Geological factors of the isotopic distribution of carbon of organic matter in sedimentary rocks

International Nuclear Information System (INIS)

Maass, J.

1981-01-01

The isotope ratio of carbon of fossile organic matter can be regarded as a definite criterion of its genetic origin. As the biofacial character of organic matter, especially the chemical composition (H/C-ratio), decisively influences the mode and quantity of the potential hydrocarbon production, isotopic analysis is an essential method for the prognostic evaluation of sedimentary basins with regard to their oil and gas perspectives. The genetic relations to the parent substance continue in the bituminization and coalification products and make it possible to apply the isotopic analysis of carbon to prospection work for hydrocarbons. (author)

Effects of ozonation and temperature on the biodegradation of natural organic matter in biological granular activated carbon filters

NARCIS (Netherlands)

Van der Aa, L.T.J.; Rietveld, L.C.; Van Dijk, J.C.

2011-01-01

Four pilot (biological) granular activated carbon ((B)GAC) filters were operated to quantify the effects of ozonation and water temperature on the biodegradation of natural organic matter (NOM) in (B)GAC filters. The removal of dissolved organic carbon (DOC), assimilable organic carbon (AOC) and

Soil organic matter

International Nuclear Information System (INIS)

1976-01-01

The nature, content and behaviour of the organic matter, or humus, in soil are factors of fundamental importance for soil productivity and the development of optimum conditions for growth of crops under diverse temperate, tropical and arid climatic conditions. In the recent symposium on soil organic matter studies - as in the two preceding ones in 1963 and 1969 - due consideration was given to studies involving the use of radioactive and stable isotopes. However, the latest symposium was a departure from previous efforts in that non-isotopic approaches to research on soil organic matter were included. A number of papers dealt with the behaviour and functions of organic matter and suggested improved management practices, the use of which would contribute to increasing agricultural production. Other papers discussed the turnover of plant residues, the release of plant nutrients through the biodegradation of organic compounds, the nitrogen economy and the dynamics of transformation of organic forms of nitrogen. In addition, consideration was given to studies on the biochemical transformation of organic matter, characterization of humic acids, carbon-14 dating and the development of modern techniques and their impact on soil organic matter research

Sequestration of carbon in soil organic matter in Senegal: an overview

Science.gov (United States)

Tieszen, Larry L.; Tappan, G. Gray; Toure, A.

2004-01-01

Sequestration of Carbon in Soil Organic Matter (SOCSOM) in Senegal is a multi-disciplinary development project planned and refined through two international workshops. The project was implemented by integrating a core of international experts in remote sensing, biogeochemical modeling, community socio-economic assessments, and carbon measurements in a fully collaborative manner with Senegal organizations, national scientists, and local knowledge and expertise. The study addresses the potential role developing countries in semi-arid areas can play in climate mitigation activities. Multiple benefits to smallholders could accrue as a result of management practices to re-establish soil carbon content lost because of land use changes or management practices that are not sustainable. The specific importance for the Sahel is because of the high vulnerability to climate change in already impoverished rural societies.

Effects of molecular weight of natural organic matter on cadmium mobility in soil environments and its carbon isotope characteristics

International Nuclear Information System (INIS)

Mahara, Y.; Kubota, T.; Wakayama, R.; Nakano-Ohta, T.; Nakamura, T.

2007-01-01

We investigated the role of natural organic matter in cadmium mobility in soil environments. We collected the dissolved organic matter from two different types of natural waters: pond surface water, which is oxic, and deep anoxic groundwater. The collected organic matter was fractionated into four groups with molecular weights (unit: Da (Daltons)) of 3 , 1-10 x 10 3 , 10-100 x 10 3 , and > 100 x 10 3 . The organic matter source was land plants, based on the carbon isotope ratios (δ 13 C/ 12 C). The organic matter in surface water originated from presently growing land plants, based on 14 C dating, but the organic matter in deep groundwater originated from land plants that grew approximately 4000 years ago. However, some carbon was supplied by the high-molecular-weight fraction of humic substances in soil or sediments. Cadmium interacted in a system of siliceous sand, fractionated organic matter, and water. The lowest molecular weight fraction of organic matter ( 3 ) bound more cadmium than did the higher molecular weight fractions. Organic matter in deep groundwater was more strongly bound to cadmium than was organic matter in surface water. The binding behaviours of organic matter with cadmium depended on concentration, age, molecular weight, and degradation conditions of the organic matter in natural waters. Consequently, the dissolved, low-molecular-weight fraction in organic matter strongly influences cadmium migration and mobility in the environment

The Role of Refractory Dissolved Organic Matter in Ocean Carbon Sequestration

DEFF Research Database (Denmark)

Jørgensen, Linda

The ocean assimilates a large amount of atmospheric CO2 and is potentially a buffer for climate change. A fraction of the assimilated CO2 is incorporated into algal biomass and further converted into refractory dissolved organic matter (DOM). Carbon bound in refractory DOM has the potential...... studies the prokaryotic production and degradation of oceanic refractory DOM and discusses the reasons for the persistent nature of this large DOM fraction. The first two papers investigate the microbial carbon pump, i.e. prokaryotic transfor-mation of organic carbon into refractory DOM. The results show...... DOM compounds in the ocean are rare—possibly too rare to sustain viable uptake and assimilation. Hence, the dilute concentration of individual compounds is a possible explanation for the apparent refractory nature of most DOM in the ocean. Understanding the mechanisms that control the quality...

TAILORING ACTIVATED CARBONS FOR ENHANCED REMOVAL OF NATURAL ORGANIC MATTER FROM NATURAL WATERS. (R828157)

Science.gov (United States)

Several pathways have been employed to systematically modify two granular activated carbons (GACs), F400 (coal-based) and Macro (wood-based), for examining adsorption of dissolved natural organic matter (DOM) from natural waters. A total of 24 activated carbons with different ...

Correlation between Soil Organic Matter, Total Organic Matter and ...

African Journals Online (AJOL)

A total of four sites distributed in different soils of Kelantan State, Malaysia was identified for the study. Soils were collected by depth interval of 0-10cm, 10-20cm and 20-30cm. The correlation of soil organic matter (SOM) content, total organic carbon (TOC) content, water content and soils texture for industrial area at ...

Carbon and nitrogen molecular composition of soil organic matter fractions resistant to oxidation

Science.gov (United States)

Katherine Heckman; Dorisel Torres; Christopher Swanston; Johannes Lehmann

2017-01-01

The methods used to isolate and characterise pyrogenic organic carbon (PyC) from soils vary widely, and there is little agreement in the literature as to which method truly isolates the most chemically recalcitrant (inferred from oxidative resistance) and persistent (inferred from radiocarbon abundance) fraction of soil organic matter. In addition, the roles of fire,...

Granular activated carbon for removal of organic matter and turbidity from secondary wastewater.

Science.gov (United States)

Hatt, J W; Germain, E; Judd, S J

2013-01-01

A range of commercial granular activated carbon (GAC) media have been assessed as pretreatment technologies for a downstream microfiltration (MF) process. Media were assessed on the basis of reduction in both organic matter and turbidity, since these are known to cause fouling in MF membranes. Isotherm adsorption analysis through jar testing with supplementary column trials revealed a wide variation between the different adsorbent materials with regard to organics removal and adsorption kinetics. Comparison with previous work using powdered activated carbon (PAC) revealed that for organic removal above 60% the use of GAC media incurs a significantly lower carbon usage rate than PAC. All GACs tested achieved a minimum of 80% turbidity removal. This combination of turbidity and organic removal suggests that GAC would be expected to provide a significant reduction in fouling of a downstream MF process with improved product water quality.

Use of carbon-14 in soil organic matter studies

International Nuclear Information System (INIS)

Vimal, O.P.; Kamath, M.B.

1974-01-01

Despite a great deal of research work on various aspects of soil organic matter, there are many gaps in the knowledge of the process of humus formation. These limitations arise mainly from the complex and heterogenous nature of soil humus substances, analytical problems in separating the fresh and decomposable materials from the old stabilized true humus substances and the lack of a clear understanding of the chemical structure of the humic acid molecule. During recent years, the use of carbon-14 has helped to trace within soil, transformation of a number of metabolites upto the point where they turn into humus. These studies have changed the concepts of the formation and stability of soil humus substances, their colloidal chemical properties and the uptake of organomolecules by plant roots. The present paper presents a synoptic view of the use of radiocarbon in studying the kinetics of humification, nature of precursors in humic acid formation, turnover of soil organic matter and the direct effects of humus substances on plant growth. (author)

Microbial control of soil organic matter mineralization responses to labile carbon in subarctic climate change treatments

DEFF Research Database (Denmark)

Rousk, Kathrin; Michelsen, Anders; Rousk, Johannes

2016-01-01

Half the global soil carbon (C) is held in high-latitude systems. Climate change will expose these to warming and a shift towards plant communities with more labile C input. Labile C can also increase the rate of loss of native soil organic matter (SOM); a phenomenon termed ‘priming’. We investig......Half the global soil carbon (C) is held in high-latitude systems. Climate change will expose these to warming and a shift towards plant communities with more labile C input. Labile C can also increase the rate of loss of native soil organic matter (SOM); a phenomenon termed ‘priming’. We...

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)

Temperature sensitivity of respiration scales with organic matter recalcitrance

Science.gov (United States)

Craine, J. M.; Fierer, N.; McLauchlan, K. K.

2010-12-01

Microbial decomposition of soil organic matter is a key process in determining the carbon sequestration potential of ecosystems and carbon fluxes to the atmosphere. Since microbial decomposition is highly sensitive to short-term changes in temperature, predicting the temperature sensitivity of microbial decomposition is critical to predicting future atmospheric carbon dioxide concentrations and feedbacks to anthropogenic warming. Fundamental principles of enzyme kinetics, embodied in the carbon-quality temperature hypothesis, predict that the temperature sensitivity of microbial decomposition should increase with increasing biochemical recalcitrance of a substrate. To test the generality of this principle, we measured the temperature sensitivity of microbial respiration of soil organic matter with serial short-term temperature manipulations over 365 days for 28 North American soils. When joined with data from similar studies that represent a wide variety of contrasts, we show that the temperature sensitivity of organic matter decomposition scales with biochemical recalcitrance. With physico-chemical protection likely an important covariate for relating plant and soil organic matter decomposition scalars, biochemically recalcitrant organic matter is highly susceptible to short-term increases in temperature, a key link in predicting the effects of warming on carbon cycling.

Content and carbon stocks in labile and recalcitrant organic matter of the soil under crop-livestock integration in Cerrado

Directory of Open Access Journals (Sweden)

Itaynara Batista

2013-12-01

Full Text Available The study of organic matter and its compartments and their relationship with management, aims to develop strategies for increasing their levels in soils and better understanding of its dynamics. This work aimed to evaluate the fractions of soil organic matter and their carbon stocks in different soil cover system in crop-livestock integration and native Cerrado vegetation. The study was conducted at the farm Cabeceira, Maracajú – MS, sample area have the following history: soybean/corn + brachiaria/cotton/oat + pasture/soybean/formation of pasture/grazing, sampling was carried out in two seasons, dry (May/2009 and rainy (March 2010, in the dry season, crops present were: pasture, corn and cotton + brachiaria and in the rainy season were corn, cotton and soybeans, so the areas in the two evaluation periods were: pasture / maize + brachiaria / cotton, cotton / soybean area and a native of Savanna. Was performed to determine the exchangeable cations, particle size analysis, bulk density, organic carbon, particle size fractionation of organic matter of the soil with the quantification of particulate organic carbon (POC and organic carbon associated with minerals (OCam. Was also quantified the carbon stock and size fractions. The area of pasture / maize showed higher carbon stock in the particulate fraction in the topsoil. The area of cotton / soy due to its lower clay, showed the greatest loss of carbon. Because of the areas have the same history, the stock of more recalcitrant fraction was not sensitive to variations in coverage. The POC fraction appears more sensitive to different soil covers and seasonality.

Phytoplankton Do Not Produce Carbon-Rich Organic Matter in High CO2 Oceans

Science.gov (United States)

Kim, Ja-Myung; Lee, Kitack; Suh, Young-Sang; Han, In-Seong

2018-05-01

The ocean is a substantial sink for atmospheric carbon dioxide (CO2) released as a result of human activities. Over the coming decades the dissolved inorganic C concentration in the surface ocean is predicted to increase, which is expected to have a direct influence on the efficiency of C utilization (consumption and production) by phytoplankton during photosynthesis. Here we evaluated the generality of C-rich organic matter production by examining the elemental C:N ratio of organic matter produced under conditions of varying pCO2. The data used in this analysis were obtained from a series of pelagic in situ pCO2 perturbation studies that were performed in the diverse ocean regions and involved natural phytoplankton assemblages. The C:N ratio of the resulting particulate and dissolved organic matter did not differ across the range of pCO2 conditions tested. In particular, the ratio for particulate organic C and N was found to be 6.58 ± 0.05, close to the theoretical value of 6.6.

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.

ORGANIC MATTER LABILE FRACTIONS AND CARBON STOCKS IN A TYPIC QUARTZIPSAMMENT CULTIVATED WITH SUGARCANE HARVESTED WITHOUT BURNING

Directory of Open Access Journals (Sweden)

JOSÉ DE SOUZA OLIVEIRA FILHO

2017-01-01

Full Text Available The permanence of sugarcane straw on the soil surface, in systems without the pre-harvest straw burning practice, directly affects the soil organic matter dynamics. The objective of this work was to evaluate the changes in total organic carbon (TOC, carbon in the light organic matter (CLOM and particulate organic carbon (POC, and their carbon stocks in a typic Quartzipsamment cultivated for nine years with sugarcane crops, which were conducted without the pre-harvest straw burning practice, in Paraipaba, State of Ceará, Brazil. Disturbed and undisturbed soil samples were collected at depths of 0.0-0.025, 0.025-0.05, 0.05-0.10, 0.10-0.20 and 0.20-0.30 m, in the sugarcane crop area and in an adjacent native forest area, in order to quantify the TOC, CLOM and POC, as well as the carbon stocks accumulated in the layer 0.0-0.30 m related to these fractions (TOCSt, CLOMSt and POCSt. TOC content changes after nine years of sugarcane crops, conducted without pre-harvest straw burning, were found only in the layers 0.10-0.20 and 0.20-0.30 m. The CLOM varied only in the layer 0.025-0.05 m. The POC content changes were more noticeable than the changes in TOC and CMOL. The CLOM of the sugarcane crop area presented high similarity with TOC, which may affect their quantification in studies related to the soil organic matter dynamics. The sugarcane crop increased the TOCSt, POCSt and CLOMSt in the layer 0.0-0.30 m, compared with the adjacent native forest area.

The Role of Physical and Human Landscape Properties on Carbon Composition of Organic Matter in Tropical Rivers

Science.gov (United States)

Ballester, M. R.; Krusche, A. V.; Victoria, R. L.; Richey, J. E.; Deegan, L.; Neill, C.

2011-12-01

To evaluate physical and human controls organic matter carbon composition in tropical rivers, we applied an integrated analysis of landscape properties and riverine isotopic composition. Our goal was to establish the relationships between basin attributes and forms and composition of dissolved and particulate organic matter in rivers. A GIS template was developed as tool to support the understanding of the biogeochemistry of the surface waters of the Ji-Paraná (Western Amazonia) and the Piracicaba (southeastern of Brazil)rivers. Each basin was divided into drainage units, organized according to river network morphology and degree of land-use impact. The delineated drainage areas were individually characterized in terms of topography, soils and land use using data sets compiled as layers in ArcGis and ERDAS-IMAGINE software. DOM and POM carbon stable isotopic composition were determined at several sites along the main tributaries and small streams. The effects of these drivers on the fluvial carbon was quantified by a multiple linear regression analysis, relating basin characteristics and river isotopic composition. The results showed that relatively recent land cover changes have already had an impact on the composition of the riverine DOM and POM, indicating that, as in natural ecosystems, the vegetation plays a key role in the composition of the riverine organic matter in agricultural systems.

Seasonal distribution of organic matter in mangrove environment of Goa

Digital Repository Service at National Institute of Oceanography (India)

Jagtap, T.G.

Water and sediments were studied for the distribution of suspended matter, organic carbon and nitrogen Suspended matter ranged from 3-373 mg.l-1 while particulate organic carbon (POC) from 0.03-9.94 mg.l-1 POC value showed significant correlation...

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

Colored dissolved organic matter in shallow estuaries: relationships between carbon sources and light attenuation

Science.gov (United States)

Oestreich, W. K.; Ganju, N. K.; Pohlman, J. W.; Suttles, S. E.

2016-02-01

Light availability is of primary importance to the ecological function of shallow estuaries. For example, benthic primary production by submerged aquatic vegetation is contingent upon light penetration to the seabed. A major component that attenuates light in estuaries is colored dissolved organic matter (CDOM). CDOM is often measured via a proxy, fluorescing dissolved organic matter (fDOM), due to the ease of in situ fDOM sensor measurements. Fluorescence must be converted to CDOM absorbance for use in light attenuation calculations. However, this CDOM-fDOM relationship varies among and within estuaries. We quantified the variability in this relationship within three estuaries along the mid-Atlantic margin of the eastern United States: West Falmouth Harbor (MA), Barnegat Bay (NJ), and Chincoteague Bay (MD/VA). Land use surrounding these estuaries ranges from urban to developed, with varying sources of nutrients and organic matter. Measurements of fDOM (excitation and emission wavelengths of 365 nm (±5 nm) and 460 nm (±40 nm), respectively) and CDOM absorbance were taken along a terrestrial-to-marine gradient in all three estuaries. The ratio of the absorption coefficient at 340 nm (m-1) to fDOM (QSU) was higher in West Falmouth Harbor (1.22) than in Barnegat Bay (0.22) and Chincoteague Bay (0.17). The CDOM : fDOM absorption ratio was variable between sites within West Falmouth Harbor and Barnegat Bay, but consistent between sites within Chincoteague Bay. Stable carbon isotope analysis for constraining the source of dissolved organic matter (DOM) in West Falmouth Harbor and Barnegat Bay yielded δ13C values ranging from -19.7 to -26.1 ‰ and -20.8 to -26.7 ‰, respectively. Concentration and stable carbon isotope mixing models of DOC (dissolved organic carbon) indicate a contribution of 13C-enriched DOC in the estuaries. The most likely source of 13C-enriched DOC for the systems we investigated is Spartina cordgrass. Comparison of DOC source to CDOM : f

Tracing the source of soil organic matter eroded from temperate forest catchments using carbon and nitrogen isotopes

Science.gov (United States)

Emma P. McCorkle; Asmeret Asefaw Berhe; Carolyn T. Hunsaker; Dale W. Johnson; Karis J. McFarlane; Marilyn L. Fogel; Stephen C. Hart

2016-01-01

Soil erosion continuously redistributes soil and associated soil organic matter (SOM) on the Earth's surface, with important implications for biogeochemical cycling of essential elements and terrestrial carbon sequestration. Despite the importance of soil erosion, surprisingly few studies have evaluated the sources of eroded carbon (C). We used natural abundance...

Age heterogeneity of soil organic matter

International Nuclear Information System (INIS)

Rethemeyer, J.; Grootes, P.M.; Bruhn, F.; Andersen, N.; Nadeau, M.J.; Kramer, C.; Gleixner, G.

2004-01-01

Accelerator mass spectrometry (AMS) radiocarbon measurements were used to investigate the heterogeneity of organic matter in soils of agricultural long-term trial sites in Germany and Great Britain. The strong age heterogeneity of the soil organic matter (SOM) is reflected by highly variable 14 C values of different organic components, ranging from modern (>100 pMC) to 7% modern carbon (pMC). At the field experiment in Halle (Germany), located in a heavily industrialized area, an increase of 14 C content with increasing depth was observed even though the input of modern plant debris should be highest in the topsoil. This is attributed to a significant contribution of old carbon (of up to 50% in the topsoil) to SOM. As a test to exclude the old carbon contamination, more specific SOM fractions were extracted. However, even a phospholipid fraction representing viable microbial biomass that is supposed to be short-lived in SOM, shows a strong influence of old, refractory carbon, when radiocarbon dated. In contrast, 14 C data of other field trials distant from industrial areas indicate that there inputs of old carbon to the soil are lower or even absent. Such locations are more favorable to study SOM stabilization and to quantify turnover of organic carbon in soils

Application of the IAS theory combining to a three compartments description of natural organic matter to the adsorption of atrazine or diuron on activated carbon.

Science.gov (United States)

Baudu, M; Raveau, D; Guibaud, G

2004-07-01

The study of natural organic matter (NOM) adsorption on an activated carbon showed that equilibrium cannot be described according to a simple model such as a Freundlich isotherm and confirms the need for a closer description of the organic matter to simulate the competitive adsorption with micropollutants. A representation of the organic matter in three fractions is chosen: non-adsorbable, weak and strong adsorbable. The Ideal Adsorbed Solution Theory (IAST) can, under restrictive conditions, be used to effectively predict the competition between the pesticides and the organic matter. Therefore, it was noted that the model simulated with good precision the competition between atrazine or diuron and natural organic matter in aqueous solution for two activated carbons (A and B). The same parameters for the modeling of organic matter adsorption (Freudlich constants for two absorbable fractions) are used with the two pesticides. However, IAST does not allow correct modeling of pesticide adsorption onto two other (C and D) activated carbons in solution in natural water to be described. IAS theory does not reveal competition between diuron and NOM and pore blockage mechanism by the NOM is proposed as the major effect for the adsorption capacity reduction. However, the difference observed between the two pesticides could be due to in addition to the pore blockage effect, a particular phenomenon with the diuron, especially with D activated carbon. We can suppose specific interactions between the diuron and the adsorbed organic matter and a competition between adsorption sites of NOM and activated carbon surface.

Stable carbon isotope analysis of soil organic matter illustrates vegetation change at the grassland/woodland boundary in southeastern Arizona, USA.

Science.gov (United States)

McPherson, G R; Boutton, T W; Midwood, A J

1993-02-01

In southeastern Arizona, Prosopis juliflora (Swartz) DC. and Quercus emoryi Torr. are the dominant woody species at grassland/woodland boundaries. The stability of the grassland/woodland boundary in this region has been questioned, although there is no direct evidence to confirm that woodland is encroaching into grassland or vice versa. We used stable carbon isotope analysis of soil organic matter to investigate the direction and magnitude of vegetation change along this ecotone. δ 13 C values of soil organic matter and roots along the ecotone indicated that both dominant woody species (C 3 ) are recent components of former grasslands (C 4 ), consistent with other reports of recent increases in woody plant abundance in grasslands and savannas throughout the world. Data on root biomass and soil organic matter suggest that this increase in woody plant abundance in grasslands and savannas may increase carbon storage in these ecosystems, with implications for the global carbon cycle.

Influence of litter diversity on dissolved organic matter release and soil carbon formation in a mixed beech forest.

Science.gov (United States)

Scheibe, Andrea; Gleixner, Gerd

2014-01-01

We investigated the effect of leaf litter on below ground carbon export and soil carbon formation in order to understand how litter diversity affects carbon cycling in forest ecosystems. 13C labeled and unlabeled leaf litter of beech (Fagus sylvatica) and ash (Fraxinus excelsior), characterized by low and high decomposability, were used in a litter exchange experiment in the Hainich National Park (Thuringia, Germany). Litter was added in pure and mixed treatments with either beech or ash labeled with 13C. We collected soil water in 5 cm mineral soil depth below each treatment biweekly and determined dissolved organic carbon (DOC), δ13C values and anion contents. In addition, we measured carbon concentrations and δ13C values in the organic and mineral soil (collected in 1 cm increments) up to 5 cm soil depth at the end of the experiment. Litter-derived C contributes less than 1% to dissolved organic matter (DOM) collected in 5 cm mineral soil depth. Better decomposable ash litter released significantly more (0.50±0.17%) litter carbon than beech litter (0.17±0.07%). All soil layers held in total around 30% of litter-derived carbon, indicating the large retention potential of litter-derived C in the top soil. Interestingly, in mixed (ash and beech litter) treatments we did not find a higher contribution of better decomposable ash-derived carbon in DOM, O horizon or mineral soil. This suggest that the known selective decomposition of better decomposable litter by soil fauna has no or only minor effects on the release and formation of litter-derived DOM and soil organic matter. Overall our experiment showed that 1) litter-derived carbon is of low importance for dissolved organic carbon release and 2) litter of higher decomposability is faster decomposed, but litter diversity does not influence the carbon flow.

Soil Organic Matter to Soil Organic Carbon ratios in recovered mountain peatlands using Vis-Nir spectroscopy approach.

Science.gov (United States)

Fernandez, Susana del Carmen; Valderrabano, Jesus; Peon, Juan Jose; Bueno, Alvaro

2015-04-01

The present research is part of a Life Project title "Inland Wetlands North of the Iberian Peninsula: Management and restoration of wetlands and hygrophilous environments" TREMEDAL (LIFE 11/ENV/ES/707) in which 25 wetland sites distributed by Galicia, Asturias, Castilla and León, País Vasco and Navarra were selected to be protected, restore or improve their conservation status and store seeds of bog plant species in the gene bank of Atlantic Botanic Garden of Gijon City, Spain. In Cantabrian Mountain Range two Poldjes (Glacio-Karstic depressions) site in Picos de Europa National Park were selected to develop an experimental action in the framework of the Life project. The selected sites harboring the most biodiverse peatland plant communities in the Cantabrian Mountain Range thus are in danger of extinction due to overgrazing. The action proposes the exclusion of livestock and wild herbivores in 5 parcels in order to contrast the differences in evolution of plant communities, hydrology and soil organic matter between grazed and non-grazed areas; and to determine future management measures that can reconcile traditional livestock raising with a better conservation of peatlands. The peatland are Vega of Liordes (Castilla-Leon) at an average altitude of 1868 m and filled mainly by clayed ferruginous sediments and Vega of Comella (Principality of Asturias) at an average altitude of 850 m and filled by at least 49 m of glacial and lacustrine sediments and 8 m of necromass from peatland vegetation. The soils developed are histosols under seasonal hydric regime in which the phreatic level suffers fluctuations over 30 cm along the year. At the time 0 (time fences were) 45 samples of the upper 15 cm of the histosols inside and outside the fences were taken. At the time 1 ( one year later) were re-sampled. Total organic carbon (TOC), Oxidizable Organic Carbon (OC), Carbonates presence and pH were analysis by chemical procedures. Also the Vis-Nir spectral analysis of the

Diagenetic fractionation of carbon isotopes in particulate and dissolved organic matter in sediments from Skan Bay, Alaska

International Nuclear Information System (INIS)

Alperin, M.J.; Reeburgh, W.S.

1991-01-01

Isotope fractionation during organic matter diagenesis was investigated by measuring detailed depth distributions of stable carbon isotope ratios in sediment particulate organic carbon (POC) and dissolved organic carbon (DOC) reservoirs. The δ 13 C value of the POC shifted systematically from -19 per-thousand at the surface to -21 per-thousand at 10 cm. Significant trends were also apparent in the δ 13 C-DOC profile. Proceeding down-core, DOC became isotopically heavier between 0 and 5 cm and isotopically lighter at greater depths. Two mechanisms could account for the observed down-core shift in δ 13 C-POC: (a) temporal changes in the isotope ratios of deposited organic matter and (b) isotope fractionation associated with diagenesis. The δ 15 C-DOC depth distribution is sensitive to which mechanism controls the isotopic composition of the POC reservoir. A diagenetic model that couples POC and DOC reservoirs was used to discriminate between temporal changes and diagenetic alteration of the POC isotopic composition. The model indicated that observed trends in δ 13 C-POC and δ 13 C-DOC depth distributions are consistent with isotopic fractionation of POC during diagenesis

Thermokarst dynamics and soil organic matter characteristics controlling initial carbon release from permafrost soils in the Siberian Yedoma region

DEFF Research Database (Denmark)

Weiss, Niels; Blok, Daan; Elberling, Bo

2016-01-01

This study relates soil organic matter (SOM) characteristics to initial soil incubation carbon release from upper permafrost samples in Yedoma region soils of northeastern Siberia, Russia. Carbon (C) and nitrogen (N) content, carbon to nitrogen ratios (C:N), δ13C and δ15N values show clear trends...

Relationships between colored dissolved organic matter and dissolved organic carbon in different coastal gradients of the Baltic Sea

OpenAIRE

Harvey, E. Therese; Kratzer, Susanne; Andersson, Agneta

2015-01-01

Due to high terrestrial runoff, the Baltic Sea is rich in dissolved organic carbon (DOC), the light-absorbing fraction of which is referred to as colored dissolved organic matter (CDOM). Inputs of DOC and CDOM are predicted to increase with climate change, affecting coastal ecosystems. We found that the relationships between DOC, CDOM, salinity, and Secchi depth all differed between the two coastal areas studied; the W Gulf of Bothnia with high terrestrial input and the NW Baltic Proper with ...

Characterization of biochars and dissolved organic matter phases obtained upon hydrothermal carbonization of Elodea nuttallii.

Science.gov (United States)

Poerschmann, J; Weiner, B; Wedwitschka, H; Zehnsdorf, A; Koehler, R; Kopinke, F-D

2015-01-01

The invasive aquatic plant Elodea nuttallii was subjected to hydrothermal carbonization at 200 °C and 240 °C to produce biochar. About 58% w/w of the organic carbon of the pristine plant was translocated into the solid biochar irrespectively of the operating temperature. The process water rich in dissolved organic matter proved a good substrate for biogas production. The E. nuttallii plants showed a high capability of incorporating metals into the biomass. This large inorganic fraction which was mainly transferred into the biochar (except sodium and potassium) may hamper the prospective application of biochar as soil amendment. The high ash content in biochar (∼ 40% w/w) along with its relatively low content of organic carbon (∼ 36% w/w) is associated with low higher heating values. Fatty acids were completely hydrolyzed from lipids due to hydrothermal treatment. Low molecular-weight carboxylic acids (acetic and lactic acid), phenols and phenolic acids turned out major organic breakdown products. Copyright © 2015 Elsevier Ltd. All rights reserved.

Molecular characterization of organic matter mobilized from Bangladeshi aquifer sediment: tracking carbon compositional change during microbial utilization

Directory of Open Access Journals (Sweden)

L. E. Pracht

2018-03-01

Full Text Available Bioavailable organic carbon in aquifer recharge waters and sediments can fuel microbial reactions with implications for groundwater quality. A previous incubation experiment showed that sedimentary organic carbon (SOC mobilized off sandy sediment collected from an arsenic-contaminated and methanogenic aquifer in Bangladesh was bioavailable; it was transformed into methane. We used high-resolution mass spectrometry to molecularly characterize this mobilized SOC, reference its composition against dissolved organic carbon (DOC in surface recharge water, track compositional changes during incubation, and advance understanding of microbial processing of organic carbon in anaerobic environments. Organic carbon mobilized off aquifer sediment was more diverse, proportionately larger, more aromatic, and more oxidized than DOC in surface recharge. Mobilized SOC was predominately composed of terrestrially derived organic matter and had characteristics signifying that it evaded microbial processing within the aquifer. Approximately 50 % of identified compounds in mobilized SOC and in DOC from surface recharge water contained sulfur. During incubation, after mobilized SOC was converted into methane, new organosulfur compounds with high S-to-C ratios and a high nominal oxidation state of carbon (NOSC were detected. We reason that these detected compounds formed abiotically following microbial reduction of sulfate to sulfide, which could have occurred during incubation but was not directly measured or that they were microbially synthesized. Most notably, microbes transformed all carbon types during incubation, including those currently considered thermodynamically unviable for microbes to degrade in anaerobic conditions (i.e., those with a low NOSC. In anaerobic environments, energy yields from redox reactions are small and the amount of energy required to remove electrons from highly reduced carbon substrates during oxidation decreases the thermodynamic

Molecular characterization of organic matter mobilized from Bangladeshi aquifer sediment: tracking carbon compositional change during microbial utilization

Science.gov (United States)

Pracht, Lara E.; Tfaily, Malak M.; Ardissono, Robert J.; Neumann, Rebecca B.

2018-03-01

Bioavailable organic carbon in aquifer recharge waters and sediments can fuel microbial reactions with implications for groundwater quality. A previous incubation experiment showed that sedimentary organic carbon (SOC) mobilized off sandy sediment collected from an arsenic-contaminated and methanogenic aquifer in Bangladesh was bioavailable; it was transformed into methane. We used high-resolution mass spectrometry to molecularly characterize this mobilized SOC, reference its composition against dissolved organic carbon (DOC) in surface recharge water, track compositional changes during incubation, and advance understanding of microbial processing of organic carbon in anaerobic environments. Organic carbon mobilized off aquifer sediment was more diverse, proportionately larger, more aromatic, and more oxidized than DOC in surface recharge. Mobilized SOC was predominately composed of terrestrially derived organic matter and had characteristics signifying that it evaded microbial processing within the aquifer. Approximately 50 % of identified compounds in mobilized SOC and in DOC from surface recharge water contained sulfur. During incubation, after mobilized SOC was converted into methane, new organosulfur compounds with high S-to-C ratios and a high nominal oxidation state of carbon (NOSC) were detected. We reason that these detected compounds formed abiotically following microbial reduction of sulfate to sulfide, which could have occurred during incubation but was not directly measured or that they were microbially synthesized. Most notably, microbes transformed all carbon types during incubation, including those currently considered thermodynamically unviable for microbes to degrade in anaerobic conditions (i.e., those with a low NOSC). In anaerobic environments, energy yields from redox reactions are small and the amount of energy required to remove electrons from highly reduced carbon substrates during oxidation decreases the thermodynamic favorability of

Colored dissolved organic matter in shallow estuaries: relationships between carbon sources and light attenuation

Science.gov (United States)

Oestreich, W.K.; Ganju, Neil K.; Pohlman, John; Suttles, Steven E.

2016-01-01

Light availability is of primary importance to the ecological function of shallow estuaries. For example, benthic primary production by submerged aquatic vegetation is contingent upon light penetration to the seabed. A major component that attenuates light in estuaries is colored dissolved organic matter (CDOM). CDOM is often measured via a proxy, fluorescing dissolved organic matter (fDOM), due to the ease of in situ fDOM sensor measurements. Fluorescence must be converted to CDOM absorbance for use in light attenuation calculations. However, this CDOM–fDOM relationship varies among and within estuaries. We quantified the variability in this relationship within three estuaries along the mid-Atlantic margin of the eastern United States: West Falmouth Harbor (MA), Barnegat Bay (NJ), and Chincoteague Bay (MD/VA). Land use surrounding these estuaries ranges from urban to developed, with varying sources of nutrients and organic matter. Measurements of fDOM (excitation and emission wavelengths of 365 nm (±5 nm) and 460 nm (±40 nm), respectively) and CDOM absorbance were taken along a terrestrial-to-marine gradient in all three estuaries. The ratio of the absorption coefficient at 340 nm (m−1) to fDOM (QSU) was higher in West Falmouth Harbor (1.22) than in Barnegat Bay (0.22) and Chincoteague Bay (0.17). The CDOM : fDOM absorption ratio was variable between sites within West Falmouth Harbor and Barnegat Bay, but consistent between sites within Chincoteague Bay. Stable carbon isotope analysis for constraining the source of dissolved organic matter (DOM) in West Falmouth Harbor and Barnegat Bay yielded δ13C values ranging from −19.7 to −26.1 ‰ and −20.8 to −26.7 ‰, respectively. Concentration and stable carbon isotope mixing models of DOC (dissolved organic carbon) indicate a contribution of 13C-enriched DOC in the estuaries. The most likely source of 13C-enriched DOC for the systems we investigated is Spartina cordgrass. Comparison of

Mercury dilution by autochthonous organic matter in a fertilized mangrove wetland.

Science.gov (United States)

Machado, Wilson; Sanders, Christian J; Santos, Isaac R; Sanders, Luciana M; Silva-Filho, Emmanoel V; Luiz-Silva, Wanilson

2016-06-01

A dated sediment core from a highly-fertilized mangrove wetland located in Cubatão (SE Brazil) presented a negative correlation between mercury (Hg) and organic carbon contents. This is an unusual result for a metal with well-known affinity to organic matter. A dilution of Hg concentrations by autochthonous organic matter explained this observation, as revealed by carbon stable isotopes signatures (δ(13)C). Mercury dilution by the predominant mangrove-derived organic matter counterbalanced the positive influences of algal-derived organic matter and clay contents on Hg levels, suggesting that deleterious effects of Hg may be attenuated. Considering the current paradigm on the positive effect of organic matter on Hg concentrations in coastal sediments and the expected increase in mangrove organic matter burial due to natural and anthropogenic stimulations of primary production, predictions on the influences of organic matter on Hg accumulation in mangrove wetlands deserve caution. Copyright © 2016 Elsevier Ltd. All rights reserved.

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.

Production of Dissolved Organic Matter During Doliolid Feeding

Science.gov (United States)

Castellane, N. J.; Paffenhofer, G. A.; Stubbins, A.

2016-02-01

The biological carbon pump (BCP) draws carbon dioxide out of the atmosphere and buries it at the seafloor. The efficiency of the BCP is determined in part by the sinking rates of particulate organic carbon (POC) from ocean surface waters. Zooplankton can package POC into fecal pellets with higher sinking rates than their food source (e.g. phytoplankton), increasing the efficiency of the BCP. However, dissolved organic carbon (DOC) is also produced as zooplankton ingest and egest food, reducing the efficiency of BCP. The pelagic tunicate Dolioletta gegenbauri (doliolid) is a gelatinous zooplankton found at high concentrations in shelf waters, including our study site: the South Atlantic Bight. Doliolids are efficient grazers capable of stripping large quantities of phytoplankton from the water column. To determine the balance between pellet formation and DOC production during feeding, doliolids (6-7 mm gonozooids) were placed in natural seawater amended with a live phytoplankton food source and incubated on a plankton wheel. Dissolved organic matter (DOM) released directly to the water as well as the water soluble fraction of pellet organic matter were quantified and optically characterized. Colored dissolved organic matter (CDOM) absorbance and fluorescence spectra revealed that doliolid feeding produces DOM with optical properties that are commonly indicative of newly produced, highly biolabile DOM of microbial origin. Based upon these optical characteristics, doliolid-produced DOM is expected to be highly bio-labile in the environment and therefore rapidly degraded by surface ocean microbes shunting phytoplankton-derived organic carbon out of the BCP and back to dissolved inorganic carbon.

Behaviour of organic matters in uranium ore processing

International Nuclear Information System (INIS)

Wu Sanmin

1991-01-01

The oxidation-reduction behaviour of organic matters in the course of oxidation roasting, acid leaching and alkali leaching, the regeneration of humic acid and the consumption of reagents are described. The mineralogical characteristics of the organic matter samples were studied. The results show that its organic matter rich in volatile carbon and with the shorter evolutionary process and lower association is easily oxidized with higher consumption of oxidant during its acid leaching; it is easily oxidized with forming humic acid during alkali leaching; and pretreating it by oxidation roasting is beneficial to the oxidation of uranium. On the contrary, the organic matter rich in fixed carbon, and with longer evolutionary process and higher association is difficultly oxidized with lower consumption of oxidant during its acid leaching; it is difficult to regenerate humic acid for it during alkali leaching; and the uranium can be easily reduced and the leaching performance of uranium can be lowered

Absorption features of chromophoric dissolved organic matter (CDOM) and tracing implication for dissolved organic carbon (DOC) in Changjiang Estuary, China

OpenAIRE

Zhang, X. Y.; Chen, X.; Deng, H.; Du, Y.; Jin, H. Y.

2013-01-01

Chromophoric dissolved organic matter (CDOM) represents the light absorbing fraction of dissolved organic carbon (DOC). Studies have shown that the optical properties of CDOM can be used to infer the distribution and diffusion characteristics of DOC in the estuary and coastal zone. The inversion of DOC concentrations from remote sensing has been implemented in certain regions. In this study we investigate the potential of tracing DOC from CDOM by the measure...

The effects of organic matter-mineral interactions and organic matter chemistry on diuron sorption across a diverse range of soils.

Science.gov (United States)

Smernik, Ronald J; Kookana, Rai S

2015-01-01

Sorption of non-ionic organic compounds to soil is usually expressed as the carbon-normalized partition coefficient (KOC), because it is assumed that the main factor that influences the amount sorbed is the organic carbon content of the soil. However, KOC can vary by a factor of at least ten across a range of soils. We investigated two potential causes of variation in diuron KOC - organic matter-mineral interactions and organic matter chemistry - for a diverse set of 34 soils from Sri Lanka, representing a wide range of soil types. Treatment with hydrofluoric acid (HF-treatment) was used to concentrate soil organic matter. HF-treatment increased KOC for the majority of soils (average factor 2.4). We attribute this increase to the blocking of organic matter sorption sites in the whole soils by minerals. There was no significant correlation between KOC for the whole soils and KOC for the HF-treated soils, indicating that the importance of organic matter-mineral interactions varied greatly amongst these soils. There was as much variation in KOC across the HF-treated soils as there was across the whole soils, indicating that the nature of soil organic matter is also an important contributor to KOC variability. Organic matter chemistry, determined by solid-state (13)C nuclear magnetic resonance (NMR) spectroscopy, was correlated with KOC for the HF-treated soils. In particular, KOC increased with the aromatic C content (R=0.64, p=1×10(-6)), and decreased with O-alkyl C (R=-0.32, p=0.03) and alkyl C (R=-0.41, p=0.004) content. Copyright © 2014 Elsevier Ltd. All rights reserved.

The effects of dissolved natural organic matter on the adsorption of synthetic organic chemicals by activated carbons and carbon nanotubes.

Science.gov (United States)

Zhang, Shujuan; Shao, Ting; Karanfil, Tanju

2011-01-01

Understanding the influence of natural organic matter (NOM) on synthetic organic contaminant (SOC) adsorption by carbon nanotubes (CNTs) is important for assessing the environmental implications of accidental CNT release and spill to natural waters, and their potential use as adsorbents in engineered systems. In this study, adsorption of two SOCs by three single-walled carbon nanotubes (SWNTs), one multi-walled carbon nanotube (MWNT), a microporous activated carbon fiber (ACF) [i.e., ACF10] and a bimodal porous granular activated carbon (GAC) [i.e., HD4000] was compared in the presence and absence of NOM. The NOM effect was found to depend strongly on the pore size distribution of carbons. Minimal NOM effect occurred on the macroporous MWNT, whereas severe NOM effects were observed on the microporous HD4000 and ACF10. Although the single-solute adsorption capacities of the SWNTs were much lower than those of HD4000, in the presence of NOM the SWNTs exhibited adsorption capacities similar to those of HD4000. Therefore, if released into natural waters, SWNTs can behave like an activated carbon, and will be able to adsorb, carry, and transfer SOCs to other systems. However, from an engineering application perspective, CNTs did not exhibit a major advantage, in terms of adsorption capacities, over the GAC and ACF. The NOM effect was also found to depend on molecular properties of SOCs. NOM competition was more severe on the adsorption of 2-phenylphenol, a nonplanar and hydrophilic SOC, than phenanthrene, a planar and hydrophobic SOC, tested in this study. In terms of surface chemistry, both adsorption affinity to SOCs and NOM effect on SOC adsorption were enhanced with increasing hydrophobicity of the SWNTs. Copyright © 2010 Elsevier Ltd. All rights reserved.

Transformation of soil organic matter in a Japanese larch forest. Radiocarbon and stable carbon isotope compositions versus soil depth

International Nuclear Information System (INIS)

Liu Wei; Moriizumi, Jun; Yamazawa, Hiromi; Iida, Takao

2008-01-01

Soil organic matter at a depth of 0-55 cm, collected from a Japanese larch forest area, was separated into particulate organic matter (size >53 μm), particulate organic matter (size 14 C and δ 13 C values were determined. The Δ 14 C values of particulate matters decreased greatly from 128 per mille to -278 per mille, indicating a relative increase of resistant organic components in particulate matters. That of humic acid matter decreased from 183 per mille to -139 per mille. For these of organic matter fractions at the same depth, the Δ 14 C values of particulate matter (size >53μm) are smallest and those of humic acid matter are the largest. That indicates that a high contribution of young organic matter to the humic acid matter exists and transformation tendency of particulate matter may be from coarse to small in the particulate size. Positive Δ 14 C values appeared at a depth of 10 cm, 25 cm, and 35 cm for the particulate organic matter (size >53μm), particulate organic matter (size 14 C values of the humic acid matter also infects that the bomb carbon has reached the depth of 35 cm. Additionally, the Δ 14 C values of these three kinds of organic matters ranged from 50 per mille to 183 per mille at a depth of 0-7 cm, which were not smaller than that of litter in the forest area, indicating high proportion of modern, plants-derived soil organic matter in this depth ranges. The δ 13 C values increased from -28 per mille to -23 per mille with the increase depth of 0-55 cm. The δ 13 C values of humic acid matter are approximately less than that of particulate matters at the same depth, which may be explained as a high contribution of young organic matter to the humic acid matter. (author)

Three-dimensional distribution of organic matter in coastal-deltaic peat : Implications for subsidence and carbon dioxide emissions by human-induced peat oxidation

NARCIS (Netherlands)

Koster, K.; Stafleu, J.; Cohen, K. M.; Stouthamer, E.; Busschers, Freek S.; Middelkoop, H.

2018-01-01

Human-induced groundwater level lowering in the Holocene coastal-deltaic plain of the Netherlands causes oxidation of peat organic matter, resulting in land subsidence and carbon dioxide (CO2) emissions. Here, a three-dimensional (3D) analysis of the distribution of the remaining peat organic matter

Is old organic matter simple organic matter?

Science.gov (United States)

Nunan, Naoise; Lerch, Thomas; Pouteau, Valérie; Mora, Philippe; Changey, Fréderique; Kätterer, Thomas; Herrmann, Anke

2016-04-01

Bare fallow soils that have been deprived of fresh carbon inputs for prolonged periods contain mostly old, stable organic carbon. In order to shed light on the nature of this carbon, the functional diversity profiles (MicroResp™, Biolog™ and enzyme activity spectra) of the microbial communities of long-term barefallow soils were analysed and compared with those of the microbial communities from their cultivated counterparts. The study was based on the idea that microbial communities adapt to their environment and that therefore the catabolic and enzymatic profiles would reflect the type of substrates available to the microbial communities. The catabolic profiles suggested that the microbial communities in the long-term bare-fallow soil were exposed to a less diverse range of substrates and that these substrates tended to be of simpler molecular forms. Both the catabolic and enzyme activity profiles suggested that the microbial communities from the long-term bare-fallow soils were less adapted to using polymers. These results do not fit with the traditional view of old, stable carbon being composed of complex, recalcitrant polymers. An energetics analysis of the substrate use of the microbial communities for the different soils suggested that the microbial communities from the long-term bare-fallow soils were better adapted to using readily oxidizable,although energetically less rewarding, substrates. Microbial communities appear to adapt to the deprivation of fresh organic matter by using substrates that require little investment.

Temporal and spatial variations in particulate matter, particulate organic carbon and attenuation coefficient in Cochin Backwaters

Digital Repository Service at National Institute of Oceanography (India)

Devi, K.S.

Nine stations over a stretch of 21 km of Periyar river estuary were sampled during January to December 1981. Particulate matter varied from 3-253 mg.1 super(1) at the surface and 24.8-257mg.1 super(1) at the bottom. Particulate organic carbon ranged...

Lessons Learned from 2 Decades of Modelling Forest Dead Organic Matter and Soil Carbon at the National Scale

Science.gov (United States)

Shaw, C.; Kurz, W. A.; Metsaranta, J.; Bona, K. A.; Hararuk, O.; Smyth, C.

2017-12-01

The Carbon Budget Model of the Canadian Forest Sector (CBM-CFS3) is a forest carbon budget model that operates on individual stands. It is applied from regional to national-scales in Canada for national and international reporting of GHG emissions and removals and in support of analyses of forest sector mitigation options and other scientific and policy questions. This presentation will review the history and continuous improvement process of representations of dead organic matter (DOM) and soil carbon modelling. Early model versions in which dead organic matter (DOM) pools only included litter, downed deadwood and soil, to the current version where these pools are estimated separately to better compare model estimates against field measurements, or new pools have been added. Uncertainty analyses consistently point at soil C pools as large sources of uncertainty. With the new ground plot measurements from the National Forest Inventory, and with a newly compiled forest soil carbon database, we have recently completed a model data assimilation exercise that helped reduce parameter uncertainties. Lessons learned from the continuous improvement process will be summarised and we will discuss how model modification have led to improved representation of DOM and soil carbon dynamics. We conclude by suggesting future research priorities that can advance DOM and soil carbon modelling in Canadian forest ecosystems.

Controls on Soil Organic Matter in Blue Carbon Ecosystems along the South Florida Coast

Science.gov (United States)

Smoak, J. M.; Rosenheim, B. E.; Moyer, R. P.; Radabaugh, K.; Chambers, L. G.; Lagomasino, D.; Lynch, J.; Cahoon, D. R.

2017-12-01

Coastal wetlands store disproportionately large amounts of carbon due to high rates of net primary productivity and slow microbial degradation of organic matter in water-saturated soils. Wide spatial and temporal variability in plant communities and soil biogeochemistry necessitate location-specific quantification of carbon stocks to improve current wetland carbon inventories and future projections. We apply field measurements, remote sensing technology, and spatiotemporal models to quantify regional carbon storage and to model future spatial variability of carbon stocks in mangroves and coastal marshes in Southwest Florida. We examine soil carbon accumulation and accretion rates on time scales ranging from decadal to millennial to project responses to climate change, including variations in inundation and salinity. Once freshwater and oligohaline wetlands are exposed to increased duration and spatial extent of inundation and salinity from seawater, soil redox potential, soil respiration, and the intensification of osmotic stress to vegetation and the soil microbial community can affect the soil C balance potentially increasing rates of mineralization.

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

Science.gov (United States)

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

Microbial bioavailability regulates organic matter preservation in marine sediments

NARCIS (Netherlands)

Koho, K. A.; Nierop, K. G. J.; Moodley, L.; Middelburg, J. J.; Pozzato, L.; Soetaert, K.; van der Plicht, J.; Reichart, G-J.; Herndl, G.

2013-01-01

Burial of organic matter (OM) plays an important role in marine sediments, linking the short-term, biological carbon cycle with the long-term, geological subsurface cycle. It is well established that low-oxygen conditions promote organic carbon burial in marine sediments. However, the mechanism

The rates of carbon cycling in several soils from AMS14C measurements of fractionated soil organic matter

International Nuclear Information System (INIS)

Trumbore, S.E.; Bonani, G.; Wolfli, W.

1990-01-01

14 C mean residence times (MRT) of fractionated organic matter are reported for three pre-bomb soil profiles. Comparisons of organic matter extracted with acid and base showed that the longest MRTs were associated with the non-acid-hydrolysable fraction. The MRT of organic matter in a soil layer represents a combination of the rates of several processes, including decay to CO 2 and transport out of the layer. In some instances (notably in the A horizon of the Podzol soil studied in this paper), the MRT is dominated by the rate of transport, rather than the rate of decay. Thus it is important to use the distribution and balance of carbon in the soil profile to assess the meaning of the MRT with respect to influencing atmospheric CO 2

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

Microbial Interactions With Dissolved Organic Matter Drive Carbon Dynamics and Community Succession

Directory of Open Access Journals (Sweden)

Xiaoqin Wu

2018-06-01

Full Text Available Knowledge of dynamic interactions between natural organic matter (NOM and microbial communities is critical not only to delineate the routes of NOM degradation/transformation and carbon (C fluxes, but also to understand microbial community evolution and succession in ecosystems. Yet, these processes in subsurface environments are usually studied independently, and a comprehensive view has been elusive thus far. In this study, we fed sediment-derived dissolved organic matter (DOM to groundwater microbes and continually analyzed microbial transformation of DOM over a 50-day incubation. To document fine-scale changes in DOM chemistry, we applied high-resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS and soft X-ray absorption spectroscopy (sXAS. We also monitored the trajectory of microbial biomass, community structure and activity over this time period. Together, these analyses provided an unprecedented comprehensive view of interactions between sediment-derived DOM and indigenous subsurface groundwater microbes. Microbial decomposition of labile C in DOM was immediately evident from biomass increase and total organic carbon (TOC decrease. The change of microbial composition was closely related to DOM turnover: microbial community in early stages of incubation was influenced by relatively labile tannin- and protein-like compounds; while in later stages the community composition evolved to be most correlated with less labile lipid- and lignin-like compounds. These changes in microbial community structure and function, coupled with the contribution of microbial products to DOM pool affected the further transformation of DOM, culminating in stark changes to DOM composition over time. Our study demonstrates a distinct response of microbial communities to biotransformation of DOM, which improves our understanding of coupled interactions between sediment-derived DOM, microbial processes, and community structure in

The forgotten part of carbon cycling: Organic matter storage and turnover in subsoils [SUBSOM

Science.gov (United States)

Marschner, B.

2013-12-01

In the past, carbon flux measurements and modelling have mostly considered the topsoil where C-concentrations, root densities and microbial activities are generally highest. However, depending on climate zone and land use, this soil compartment contains only 30-50% of the C-stocks of the first meter. If the deeper subsoil down to 3 m is also considered, the contribution of topsoil carbon stocks to total soil C-pools is only 20-40%. Another distinct property of subsoil organic matter is its high apparent 14C age. The 14C age of bulk soil organic matter below 30 cm depth generally increases continuously indicating mean residence times of several 103 to 104 years. Large pool size and high radiocarbon age suggest that subsoil OM has accumulated at very low rates over very long time periods and therefore appears to be very stable. In a review, several hypotheses for explaining why subsoil SOM is so seemingly old and inert are presented. Then a recently granted German research unit consisting of 9 subprojects from all soil science disciplines is introduced, which addresses these questions using field measurements of C-fluxes, 14C analyses and conducting field and lab experiments. 40-60% of soil C-pools are found below 40 cm depth (Data from Jobbagy & Jackson 2000).

Soil carbon dynamics inferred from carbon isotope compositions of soil organic matter and soil respiration

International Nuclear Information System (INIS)

Koarashi, Jun; Asano, Tomohiro; Iida, Takao; Moriizumi, Jun

2004-01-01

To better understand 14 C cycling in terrestrial ecosystems, 14 C abundances were evaluated for fractionated soil organic matter (SOM) and soil respiration in an urban forest. In 2001 soil profile, Δ 14 C values of litter and bulk SOM increased rapidly from litter surface (62.7 per mille) to uppermost mineral soil layer (244.9 per mille), and then decreased sharply to 6 cm depth of mineral soil (125.0 per mille). Carbon enriched in 14 C by atmospheric nuclear weapons testing had penetrated to at least 16 cm depth of mineral soil. The average Δ 14 C in atmospheric CO 2 was 58.8 per mille in August 2001, suggesting recent carbon input to the topmost litter layer. Although a similar depth distribution was observed for Δ 14 C values of residual SOM after acid hydrolysis, the Δ 14 C values were slightly lower than those in bulk SOM. This indicates input of 'bomb' C into this organic fraction and higher 14 C abundance in acid-soluble SOM. The most of CO 2 may be derived from the microbial decomposition of the acid-soluble, or labile, SOM. Therefore, the labile SOM may become most influential pool for soil carbon cycling. In contrast, carbon in base-insoluble SOM remained considerably low in 14 C abundance at all depths, suggesting no or little incorporation of 'bomb' C to this fraction. Values of Δ 14 C in soil respiration ranged from 91.9 to 146.4 per mille in August 2001, showing a significant contribution from decomposition of SOM fixed over past 2-40 years. These results indicate that the use of bulk SOM as a representative of soil carbon pool would lead to severe misunderstand of the soil C dynamics on decadal and shorter time scales. (author)

Dissolved organic carbon and chromophoric dissolved organic matter properties of rivers in the USA

Science.gov (United States)

Spencer, Robert G. M.; Butler, Kenna D.; Aiken, George R.

2012-09-01

Dissolved organic carbon (DOC) concentration and chromophoric dissolved organic matter (CDOM) parameters were measured over a range of discharge in 30 U.S. rivers, covering a diverse assortment of fluvial ecosystems in terms of watershed size and landscape drained. Relationships between CDOM absorption at a range of wavelengths (a254, a350, a440) and DOC in the 30 watersheds were found to correlate strongly and positively for the majority of U.S. rivers. However, four rivers (Colorado, Colombia, Rio Grande and St. Lawrence) exhibited statistically weak relationships between CDOM absorption and DOC. These four rivers are atypical, as they either drain from the Great Lakes or experience significant impoundment of water within their watersheds, and they exhibited values for dissolved organic matter (DOM) parameters indicative of autochthonous or anthropogenic sources or photochemically degraded allochthonous DOM and thus a decoupling between CDOM and DOC. CDOM quality parameters in the 30 rivers were found to be strongly correlated to DOM compositional metrics derived via XAD fractionation, highlighting the potential for examining DOM biochemical quality from CDOM measurements. This study establishes the ability to derive DOC concentration from CDOM absorption for the majority of U.S. rivers, describes characteristics of riverine systems where such an approach is not valid, and emphasizes the possibility of examining DOM composition and thus biogeochemical function via CDOM parameters. Therefore, the usefulness of CDOM measurements, both laboratory-based analyses and in situ instrumentation, for improving spatial and temporal resolution of DOC fluxes and DOM dynamics in future studies is considerable in a range of biogeochemical studies.

Dissolved organic carbon and chromophoric dissolved organic matter properties of rivers in the USA

Science.gov (United States)

Spencer, Robert G.M.; Butler, Kenna D.; Aiken, George R.

2012-01-01

Dissolved organic carbon (DOC) concentration and chromophoric dissolved organic matter (CDOM) parameters were measured over a range of discharge in 30 U.S. rivers, covering a diverse assortment of fluvial ecosystems in terms of watershed size and landscape drained. Relationships between CDOM absorption at a range of wavelengths (a254, a350, a440) and DOC in the 30 watersheds were found to correlate strongly and positively for the majority of U.S. rivers. However, four rivers (Colorado, Colombia, Rio Grande and St. Lawrence) exhibited statistically weak relationships between CDOM absorption and DOC. These four rivers are atypical, as they either drain from the Great Lakes or experience significant impoundment of water within their watersheds, and they exhibited values for dissolved organic matter (DOM) parameters indicative of autochthonous or anthropogenic sources or photochemically degraded allochthonous DOM and thus a decoupling between CDOM and DOC. CDOM quality parameters in the 30 rivers were found to be strongly correlated to DOM compositional metrics derived via XAD fractionation, highlighting the potential for examining DOM biochemical quality from CDOM measurements. This study establishes the ability to derive DOC concentration from CDOM absorption for the majority of U.S. rivers, describes characteristics of riverine systems where such an approach is not valid, and emphasizes the possibility of examining DOM composition and thus biogeochemical function via CDOM parameters. Therefore, the usefulness of CDOM measurements, both laboratory-based analyses and in situ instrumentation, for improving spatial and temporal resolution of DOC fluxes and DOM dynamics in future studies is considerable in a range of biogeochemical studies.

Can particulate organic matter reveal emerging changes in soil organic carbon?

DEFF Research Database (Denmark)

Simonsson, Magnus; Kirchmann, Holger; Magid, Jakob

2014-01-01

different cropping systems, N fertilizer applications, and organic amendments, we found that C and N in the fine to medium sand fraction (0.063-0.600 mm, "Fraction B") showed considerably larger relative errors according to ANOVA (RMSE was 11-20% of the mean), slightly lower values of the F statistic......This study assessed whether particulate organic matter (POM) in sand fractions, isolated by wet sieving after treatment with Na hexametaphosphate, can be a sensitive indicator of incipient changes in the content and composition of soil organic matter. In five long-term field experiments including......, and slightly less contrast between treatments than total organic C and N (RMSE 3-9% of the mean). Imprecision in laboratory procedures only explained part of the increase in RMSE for C and N in Fraction B compared with total C and N; within-field spatial variability most likely had a greater influence...

Characterization of organic matter in lake sediments from Minnesota and Yellowstone National Park

Science.gov (United States)

Dean, Walter E.

2006-01-01

Samples of sediment from lakes in Minnesota and Yellowstone National Park (YNP) were analyzed for organic carbon (OC), hydrogen richness by Rock-Eval pyrolysis, and stable carbon- and nitrogen-isotope composition of bulk organic matter. Values of delta 13C of lake plankton tend to be around -28 to -32 parts per thousand (0/00). Organic matter with values of delta 13C in the high negative 20s overlap with those of organic matter derived from C3 higher terrestrial plants but are at least 10 0/00 more depleted in 13C than organic matter derived from C4 terrestrial plants. If the organic matter is produced mainly by photosynthetic plankton and is not oxidized in the water column, there may be a negative correlation between H-richness (Rock-Eval pyrolysis H-index) and delta 13C, with more H-rich, algal organic matter having lower values of delta 13C. However, if aquatic organic matter is oxidized in the water column, or if the organic matter is a mixture of terrestrial and aquatic organic matter, then there may be no correlation between H-richness and carbon-isotopic composition. Values of delta 13C lower than about -28 0/00 probably indicate a contribution of bacterial biomass produced in the hypolimnion by chemoautotrophy or methanotrophy. In highly eutrophic lakes in which large amounts of 13C-depleted organic matter is continually removed from the epilimnion by photosynthesis throughout the growing season, the entire carbon reservoir in the epilimnion may become severely 13C-enriched so that 13C-enriched photosynthetic organic matter may overprint 13C-depleted chemosynthetic bacterial organic matter produced in the hypolimnon. Most processes involved with the nitrogen cycle in lakes, such as production of ammonia and nitrate, tend to produce 15N-enriched values of delta 15N. Most Minnesota lake sediments are 15N-enriched. However, some of the more OC-rich sediments have delta 15N values close to zero (delta 15N of air), suggesting that organic matter production is

Effects of organic matter and ageing on the bioaccessibility of arsenic

International Nuclear Information System (INIS)

Meunier, Louise; Koch, Iris; Reimer, Kenneth J.

2011-01-01

Arsenic-contaminated soils may pose a risk to human health. Redevelopment of contaminated sites may involve amending soils with organic matter, which potentially increases arsenic bioaccessibility. The effects of ageing on arsenic-contaminated soils mixed with peat moss were evaluated in a simulated ageing period representing two years, during which arsenic bioaccessibility was periodically measured. Significant increases (p = 0.032) in bioaccessibility were observed for 15 of 31 samples tested, particularly in comparison with samples originally containing >30% bioaccessible arsenic in soils naturally rich in organic matter (>25%). Samples where percent arsenic bioaccessibility was unchanged with age were generally poor in organic matter (average 7.7%) and contained both arsenopyrite and pentavalent arsenic forms that remained unaffected by the organic matter amendments. Results suggest that the addition of organic matter may lead to increases in arsenic bioaccessibility, which warrants caution in the evaluation of risks associated with redevelopment of arsenic-contaminated land. - Highlights: → Adding organic matter to contaminated soils may increase arsenic bioaccessibility. → Ageing soils with >25% organic matter can lead to increased arsenic bioaccessibility. → No changes in arsenic bioaccessibility for soils poor in organic matter (mean 7.7%). → No changes in arsenic bioaccessibility for samples containing arsenopyrite. → Organic matter in soil may favour oxidation of trivalent arsenic to pentavalent form. - Adding organic carbon may increase arsenic bioaccessibility, especially in samples originally containing >30% bioaccessible arsenic in organic carbon-rich soils (>25%).

Investigating Photosensitized Properties of Natural Organic Matter and Effluent Organic Matter

KAUST Repository

Niu, Xi-Zhi

2013-05-01

The photosensitized processes significantly enhance photolysis of various chemicals in the aqueous system with dissolved organic matter (DOM) as sensitizer. The excitation of chromophores on the DOM molecule further generates reactive species as triplet states DOM, singlet oxygen, hydroxyl radical, carbonate radical etc. We investigated the photosensitization properties of Beaufort Fulvic Acid, Suwannee River Fulvic Acid, South Platte River Fulvic Acid, and Jeddah wastewater treatment plant effluent organic matter with a sunlight simulator. DOM photochemical properties were characterized by observing their performances in 3DOM*, singlet oxygen, hydroxyl radical production with indirect probing protocols. Sensitized degradation of 0.1 μM and 0.02 μM 2, 4, 6- Trimethylphenol exhibited higher pseudo-first-order rate constant than that of 10 μM. Pre-irradiated DOMs were found to be depressed in photochemical properties. Photolysis of 5 different contaminants: ibuprofen, bisphenol A, acetaminophen, cimetidine, and caffeine were found to be enhanced in the presence of sensitizers. The possible reaction pathways were revealed. Long time irradiance induced change in contaminants degradation kinetics in some DOM solutions, which was proposed to be due to the irradiation initiated indirect transformation of DOMs. Key Words: Photolysis Dissolved Organic Matter, Triplet State DOM, Singlet Oxygen, Hydroxyl Radical, Contaminants Degradation.

Elucidating Microbial Species-Specific Effects on Organic Matter Transformation in Marine Sediments

Science.gov (United States)

Mahmoudi, N.; Enke, T. N.; Beaupre, S. R.; Teske, A.; Cordero, O. X.; Pearson, A.

2017-12-01

Microbial transformation and decomposition of organic matter in sediments constitutes one of the largest fluxes of carbon in marine environments. Mineralization of sedimentary organic matter by microorganisms results in selective degradation such that bioavailable or accessible compounds are rapidly metabolized while more recalcitrant, complex compounds are preserved and buried in sediment. Recent studies have found that the ability to use different carbon sources appears to vary among microorganisms, suggesting that the availability of certain pools of carbon can be specific to the taxa that utilize the pool. This implies that organic matter mineralization in marine environments may depend on the metabolic potential of the microbial populations that are present and active. The goal of our study was to investigate the extent to which organic matter availability and transformation may be species-specific using sediment from Guaymas Basin (Gulf of California). We carried out time-series incubations using bacterial isolates and sterilized sediment in the IsoCaRB system which allowed us to measure the production rates and natural isotopic signatures (δ13C and Δ14C) of microbially-respired CO2. Separate incubations using two different marine bacterial isolates (Vibrio sp. and Pseudoalteromonas sp.) and sterilized Guaymas Basin sediment under oxic conditions showed that the rate and total quantity of organic matter metabolized by these two species differs. Approximately twice as much CO2 was collected during the Vibrio sp. incubation compared to the Pseudoalteromonas sp. incubation. Moreover, the rate at which organic matter was metabolized by the Vibrio sp. was much higher than the Pseudoalteromonas sp. indicating the intrinsic availability of organic matter in sediments may depend on the species that is present and active. Isotopic analyses of microbially respired CO2 will be used to constrain the type and age of organic matter that is accessible to each species

Vulnerability of permafrost carbon to global warming. Part I: model description and role of heat generated by organic matter decomposition

Energy Technology Data Exchange (ETDEWEB)

Khvorostyanov, D.V.; Ciais, G. (Laboratoire des Sciences du Climat et l' Environnement, Saclay (France)); Krinner, G. (Laboratoire de Glaciologie et Geophysique de l' Environnement, St Martin d' Heres (France)). e-mail: Dimitry.Khvorostiyanov@lsce.ipsl.fr; Heimann, M. (Max-Planck Inst. of Biogeochemistry, Jena (DE)); Zimov, S.A. (Northeast Science Station, Cherskii (RU))

2008-07-01

We constructed a new model to study the sensitivity of permafrost carbon stocks to future climate warming. The one-dimensional model solves an equation for diffusion of heat penetrating from the overlying atmosphere and takes into account additional in situ heat production by active soil microorganisms. Decomposition of frozen soil organic matter and produced CO{sub 2} and methane fluxes result from an interplay of soil heat conduction and phase transitions, respiration, methanogenesis and methanotrophy processes. Respiration and methanotrophy consume soil oxygen and thus can only develop in an aerated top-soil column. In contrast, methanogenesis is not limited by oxygen and can be sustained within the deep soil, releasing sufficient heat to further thaw in depth the frozen carbon-rich soil organic matter. Heat production that accompanies decomposition and methanotrophy can be an essential process providing positive feedback to atmospheric warming through self-sustaining transformation of initially frozen soil carbon into CO{sub 2} and CH{sub 4}. This supplementary heat becomes crucial, however, only under certain climate conditions. Oxygen limitation to soil respiration slows down the process, so that the mean flux of carbon released during the phase of intense decomposition is more than two times less than without oxygen limitation. Taking into account methanogenesis increases the mean carbon flux by 20%. Part II of this study deals with mobilization of frozen carbon stock in transient climate change scenarios with more elaborated methane module, which makes it possible to consider more general cases with various site configurations. Part I (this manuscript) studies mobilization of 400 GtC carbon stock of the Yedoma in response to a stepwise rapid warming focusing on the role of supplementary heat that is released to the soil during decomposition of organic matter

The response of soil carbon storage and microbially mediated carbon turnover to simulated climatic disturbance in a northern peatland forest. Revisiting the concept of soil organic matter recalcitrance

Energy Technology Data Exchange (ETDEWEB)

Kostka, Joel [Georgia Inst. of Technology, Atlanta, GA (United States)

2015-09-14

The goal of this project was to investigate changes in the structure of dissolved and solid phase organic matter, the production of CO₂ and CH₄, and the composition of decomposer microbial communities in response to the climatic forcing of environmental processes that determine the balance between carbon gas production versus storage and sequestration in peatlands. Cutting-edge analytical chemistry and next generation sequencing of microbial genes were been applied to habitats at the Marcell Experimental Forest (MEF), where the US DOE’s Oak Ridge National Laboratory and the USDA Forest Service are constructing a large-scale ecosystem study entitled, “Spruce and Peatland Responses Under Climatic and Environmental Change”(SPRUCE). Our study represented a comprehensive characterization of the sources, transformation, and decomposition of organic matter in the S1 bog at MEF. Multiple lines of evidence point to distinct, vertical zones of organic matter transformation: 1) the acrotelm consisting of living mosses, root material, and newly formed litter (0-30 cm), 2) the mesotelm, a mid-depth transition zone (30-75 cm) characterized by labile organic C compounds and intense decomposition, and 3) the underlying catotelm (below 75cm) characterized by refractory organic compounds as well as relatively low decomposition rates. These zones are in part defined by physical changes in hydraulic conductivity and water table depth. O-alkyl-C, which represents the carbohydrate fraction in the peat, was shown to be an excellent proxy for soil decomposition rates. The carbon cycle in deep peat was shown to be fueled by modern carbon sources further indicating that hydrology and surface vegetation play a role in belowground carbon cycling. We provide the first metagenomic study of an ombrotrophic peat bog, with novel insights into microbial specialization and functions in this unique terrestrial ecosystem. Vertical structuring of microbial communities

Soil aggregates, organic matter turnover and carbon balance in a Mediterranean eroded vineyard

Science.gov (United States)

Novara, Agata; Lo Papa, Giuseppe; Dazzi, Carmelo; Gristina, Luciano; Cerdà, Artemi

2014-05-01

The carbon cycle is being affected by the human impacts (Novara et al., 2011; Yan-Gui et al., 2013), and one of those is the intensification in the soil erosion in agriculture land (Cerdà et al., 2009; García Orenes et al., 2009). Vineyards also are affected by the human activities (Fernández Calviño, 2012). Vineyards in Sicily are cultivated on 110.000 ha, 10% of which on >10% slope. Deficiencies of soil organic matter are typical of the semi arid Mediterranean environment especially where traditional intensive cropping practices are adopted (Novara et al., 2012; 2013). These practices in vineyards could lead soil to intensive erosion processes (Novara et al., 2011). The fate of SOC under erosion processes is difficult to understand because of the influence of the erosion impact on SOC pathway, which depends on the different features of the process involved (detachment, transport and/or deposition). Soil erosion must be considered a net C source (Lal, 2003), as eroded soils have lower net primary productivity (NPP) (Dick and Gregorich, 2004) caused by reduction in the effective rooting depth and all in all determining decline in soil quality. Breakdown of aggregates and soil dispersion expose SOM to microbial/enzymatic processes and chemical soil properties (Dimoyiannis, 2012; Kocyigit and Demirci, 2012). Moreover the light fraction, transported by runoff, is labile and easily mineralized determining CO2 emission in the atmosphere (Jacinthe and Lal, 2004). Therefore, the carbon pool is lower in eroded than in un-eroded soil scapes and the rate of mineralization of soil organic matter is higher in sediments than in original soil. In this survey we show a research conducted on a slope sequence of three soil profiles in an irrigated vineyard located in Sambuca di Sicilia, Italy (UTM33-WGS84: 4169367N; 325011E). The SOC content was measured at depth intervals of 10 cm up to a depth of 60 cm in each pedon. Wet aggregate-size fractions with no prior chemical

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

Chemical examination of the organic matter in oil shales

Energy Technology Data Exchange (ETDEWEB)

Robertson, J B

1914-01-01

The analyses of Broxburn (Scotland), Pumpherston (Scotland), Armadale (Scotland), Australian, and Knightsbridge oil shales were given. Also, the action of nitric acid and solvents on some of the oil shales was determined. Carbon-hydrogen ratios of the oil shales varied from 6 to more than 8, and the shales with the lowest ratio (most hydrogen per carbon) produced the largest amount of oil from a given amount of organic matter. There was little resinous material in the oil shales, and most of the organic matter was insoluble in organic solvents. Nitric acid oxidized Australian torbanite, Broxburn shale, New Battle cannel coal (Scotland), and Glenfullock peat to organic acids. The hydrogen content of the organic acids obtained by oxidizing the following materials increased from ordinary coal to cannel coal to peat to Broxburn shale to torbanite. The organic substance in oil shale is a decomposition product of vegetable matter similar to that found in peat and cannel coal, and it was produced by a definite combination of external conditions.

The impact of vegetation on sedimentary organic matter composition and PAH desorption

Energy Technology Data Exchange (ETDEWEB)

Nichols, Elizabeth Guthrie [North Carolina State University, Department of Forestry and Environmental Resources, 2800 Faucette Drive, Raleigh, NC 27695 (United States)], E-mail: elizabeth_nichols@ncsu.edu; Gregory, Samuel T.; Musella, Jennifer S. [North Carolina State University, Department of Forestry and Environmental Resources, 2800 Faucette Drive, Raleigh, NC 27695 (United States)

2008-12-15

Relationships between sedimentary organic matter (SOM) composition and PAH desorption behavior were determined for vegetated and non-vegetated refinery distillate waste sediments. Sediments were fractionated into size, density, and humin fractions and analyzed for their organic matter content. Bulk sediment and humin fractions differed more in organic matter composition than size/density fractions. Vegetated humin and bulk sediments contained more polar organic carbon, black carbon, and modern (plant) carbon than non-vegetated sediment fractions. Desorption kinetics of phenanthrene, pyrene, chrysene, and C{sub 3}-phenanthrene/anthracenes from humin and bulk sediments were investigated using Tenax beads and a two-compartment, first-order kinetic model. PAH desorption from distillate waste sediments appeared to be controlled by the slow desorbing fractions of sediment; rate constants were similar to literature values for k{sub slow} and k{sub veryslow}. After several decades of plant colonization and growth (Phragmites australis), vegetated sediment fractions more extensively desorbed PAHs and had faster desorption kinetics than non-vegetated sediment fractions. - Plants alter sediment organic matter composition and PAH desorption behavior.

The impact of vegetation on sedimentary organic matter composition and PAH desorption

International Nuclear Information System (INIS)

Nichols, Elizabeth Guthrie; Gregory, Samuel T.; Musella, Jennifer S.

2008-01-01

Relationships between sedimentary organic matter (SOM) composition and PAH desorption behavior were determined for vegetated and non-vegetated refinery distillate waste sediments. Sediments were fractionated into size, density, and humin fractions and analyzed for their organic matter content. Bulk sediment and humin fractions differed more in organic matter composition than size/density fractions. Vegetated humin and bulk sediments contained more polar organic carbon, black carbon, and modern (plant) carbon than non-vegetated sediment fractions. Desorption kinetics of phenanthrene, pyrene, chrysene, and C 3 -phenanthrene/anthracenes from humin and bulk sediments were investigated using Tenax beads and a two-compartment, first-order kinetic model. PAH desorption from distillate waste sediments appeared to be controlled by the slow desorbing fractions of sediment; rate constants were similar to literature values for k slow and k veryslow . After several decades of plant colonization and growth (Phragmites australis), vegetated sediment fractions more extensively desorbed PAHs and had faster desorption kinetics than non-vegetated sediment fractions. - Plants alter sediment organic matter composition and PAH desorption behavior

Organic matter in North Bohemian Tertiavy and Cretaceous sediments with uranium mineralization

International Nuclear Information System (INIS)

Simanek, V.

1979-01-01

Significant variability was found in the qualitative and the quantitative compositions of dispersed organic matter in Tertiary rocks with uranium ore content between hundredths and units of percentage of the rocks. In Cretaceous rocks with similar proportion of uranium in w.% the variability is much smaller. In rocks with higher organic carbon and uranium levels the organic matter is in a more advanced stage of carbonification metamorphosis than in rocks with lower levels of the components. A statistical correlation test showed free positive correlation between the levels of uranium and organic carbon and the levels of uranium and strongly carbonified organic components and negative correlation between uranium level and humic substances on one hand and the uranium level and bitumens on the other. In Cretaceous sediments, the individual organic compounds were analytically determined in addition to the total level of organic carbon, the strongly carbonified organic components, humic substances and bitumens. Higher fatty acids in ppm concentrations were also found. Their distribution corresponds to the usual distribution in sediments. Rocks with lower contents of organic matter and uranium usually contain phenol aldehydes bound to glycosides while those with higher contents of uranium and organic carbon contain higher amounts of free phenol aldehydes. The composition of amino acids indicates genetic links to the microbial activity. (author)

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

Science.gov (United States)

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

2016-01-01

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

Methods for Determining Organic Matter and Colour in Water

Directory of Open Access Journals (Sweden)

Ramunė Albrektienė

2011-02-01

Full Text Available The article examines different methods for determining organic matter and colour in water. Most of organic compounds in water have a humic substance. These substances frequently form complexes with iron. Humic matter gives water a yellow-brownish colour. Water filtration through conventional sand filters does not remove colour and organic compounds, and therefore complicated water treatment methods shall be applied. The methods utilized for organic matter determination in water included research on total organic carbon, permanganate index and the bichromate number of UV absorption of 254 nm wave length. The obtained results showed the greatest dependence between water colour and permanganate index. However, UV adsorption could be used for organic matter determination during the operation of a water treatment plant and the start-up of plants as easy and fast methods.Article in Lithuanian

Overestimation of Crop Root Biomass in Field Experiments Due to Extraneous Organic Matter.

Science.gov (United States)

Hirte, Juliane; Leifeld, Jens; Abiven, Samuel; Oberholzer, Hans-Rudolf; Hammelehle, Andreas; Mayer, Jochen

2017-01-01

Root biomass is one of the most relevant root parameters for studies of plant response to environmental change, soil carbon modeling or estimations of soil carbon sequestration. A major source of error in root biomass quantification of agricultural crops in the field is the presence of extraneous organic matter in soil: dead roots from previous crops, weed roots, incorporated above ground plant residues and organic soil amendments, or remnants of soil fauna. Using the isotopic difference between recent maize root biomass and predominantly C3-derived extraneous organic matter, we determined the proportions of maize root biomass carbon of total carbon in root samples from the Swiss long-term field trial "DOK." We additionally evaluated the effects of agricultural management (bio-organic and conventional), sampling depth (0-0.25, 0.25-0.5, 0.5-0.75 m) and position (within and between maize rows), and root size class (coarse and fine roots) as defined by sieve mesh size (2 and 0.5 mm) on those proportions, and quantified the success rate of manual exclusion of extraneous organic matter from root samples. Only 60% of the root mass that we retrieved from field soil cores was actual maize root biomass from the current season. While the proportions of maize root biomass carbon were not affected by agricultural management, they increased consistently with soil depth, were higher within than between maize rows, and were higher in coarse (>2 mm) than in fine (≤2 and >0.5) root samples. The success rate of manual exclusion of extraneous organic matter from root samples was related to agricultural management and, at best, about 60%. We assume that the composition of extraneous organic matter is strongly influenced by agricultural management and soil depth and governs the effect size of the investigated factors. Extraneous organic matter may result in severe overestimation of recovered root biomass and has, therefore, large implications for soil carbon modeling and estimations

Chemical Structure of Insoluble Organic Matter of Meteorites

Science.gov (United States)

Derenne, S.; Robert, F.; Binet, L.; Gourier, D.; Rouzaud, J.-N.; Largeau, C.

A detailed knowledge of the insoluble organic matter (IOM) of the meteorites is essential to estimate to what extent the interstellar organic matter was preserved during the formation of the solar system and to decipher the synthetic pathways of this matter in space. Although predominant, the insoluble organic fraction has been much less extensively studied than soluble one due to specific analytical difficulties. The present work reports the examination of the IOM of two carbonaceous meteorites, Orgueil and Murchison through a number of various spectroscopic and microscopic methods, i. e. XANES for sulphur, carbon and nitrogen, solid state 13C NMR, electron paramagnetic resonance, electron nuclear double resonance and high resolution transmission electron microscopy.

Carbon-isotope stratigraphy from terrestrial organic matter through the Monterey event, Miocene, New Jersey margin (IODP Expedition 313)

DEFF Research Database (Denmark)

Fang, Linhao; Bjerrum, Christian J.; Hesselbo, Stephen P.

2013-01-01

documented from oceanic settings (i.e., lack of positive excursion of carbon-isotope values in terrestrial organic matter through the Langhian Stage). Factors that may potentially bias local terrestrial carbon-isotope records include reworking from older deposits, degradation and diagenesis, as well....../or reworking of older woody phytoclasts, but where such processes have occurred they do not readily explain the observed carbon-isotope values. It is concluded that the overall carbon-isotope signature for the exchangeable carbon reservoir is distorted, to the extent that the Monterey event excursion...... is not easily identifiable. The most likely explanation is that phytoclast reworking has indeed occurred in clinoform toe-of-slope facies, but the reason for the resulting relatively heavy carbon-isotope values in the Burdigalian remains obscure....

Organic matter and soil structure in the Everglades Agricultural Area

Energy Technology Data Exchange (ETDEWEB)

Wright, Alan L. [Univ. of Florida, Gainesville, FL (United States); Hanlon, Edward A. [Univ. of Florida, Gainesville, FL (United States)

2013-01-01

This publication pertains to management of organic soils (Histosols) in the Everglades Agricultural Area (EAA). These former wetland soils are a major resource for efficient agricultural production and are important globally for their high organic matter content. Recognition of global warming has led to considerable interest in soils as a repository for carbon. Soils rich in organic matter essentially sequester or retain carbon in the profile and can contribute directly to keeping that sequestered carbon from entering the atmosphere. Identification and utilization of management practices that minimize the loss of carbon from organic soils to the atmosphere can minimize effects on global warming and increase the longevity of subsiding Histosols for agricultural use. Understanding and predicting how these muck soils will respond to current and changing land uses will help to manage soil carbon. The objectives of this document are to: a. Discuss organic soil oxidation relative to storing or releasing carbon and nitrogen b. Evaluate effects of cultivation (compare structure for sugarcane vs. uncultivated soil) Based upon the findings from the land-use comparison (sugarcane or uncultivated), organic carbon was higher with cultivation in the lower depths. There is considerable potential for minimum tillage and residue management to further enhance carbon sequestration in the sugarcane system. Carbon sequestration is improved and soil subsidence is slowed with sugarcane production, and both of these are positive outcomes. Taking action to increase or maintain carbon sequestration appears to be appropriate but may introduce some risk to farming operations. Additional management methods are needed to reduce this risk. For both the longevity of these organic soils and from a global perspective, slowing subsidence through BMP implementation makes sense. Since these BMPs also have considerable societal benefit, it remains to be seen if society will help to offset a part or all

A Chemical Comparison of STARDUST Organics with Insoluble Organic Matter in Chondritic Meteorites

Science.gov (United States)

Cody, G. D.; Yabuta, H.; Alexander, C. M.; Araki, T.; Kilcoyne, D.

2006-12-01

We have analyzed 15 organic rich particles extracted from the aerogel capture device flown on the STARDUST mission spacecraft to comet Wild 2 using C-, N-, and O-X-ray Absorption Near Edge Structure (XANES) spectroscopy. Data were acquired with the Scanning Transmission X-ray Microscopy (STXM) beam line 5.3.2 at the Advanced Light Source, Lawrence Berkeley Laboratory. XANES can provide both quantitative molecular functional group information and atomic N/C and O/C data. We use these data to place the organic matter extracted from the Aerogel Capture device in context with a large database of C-, N-, and O-XANES spectra obtained on meteoritic Insoluble Organic Matter (IOM) obtained from type 1, 2, and 3 chondrites. We find that the organic chemistry of the particles extracted from aerogel varies in functional group abundances, but is universally very rich in heteroatoms (N and O). In several cases the organic carbon is closely associated with silica (possibly derived from the aerogel), but at a concentration far in excess of the intrinsic carbon abundance of synthesized (and flown) aerogel. Independently, 29-Si, 13-C, and 1-H solid state NMR was applied to analyze the nature of organic carbon present in the aerogel as byproduct of the synthesis. The intrinsic aerogel carbon is very simple in its functional group chemistry, very low in abundance, and differs completely from that detected in the extracted organic particles.

Effect of Three Types of Exogenous Organic Carbon on Soil Organic Matter and Physical Properties of a Sandy Technosol

Directory of Open Access Journals (Sweden)

Paul Robin

2018-04-01

Full Text Available Technosols made by covering agricultural soils with coastal sediments need additional organic matter (OM to be suitable for agricultural use. Climate change will likely increase the frequency and intensity of droughts in several areas. The choice of the nature and quantity of OM to add depends on dose-response curves for soil quality. This study quantifies the influence of three contrasting organic materials (vermicompost (VF, green waste compost (GWC and dairy manure (DM on four soil properties: soil organic carbon, evaporation rate, bulk density and structural stability. Soil was sampled in April and May 2014 in an artificial crop field of the vegetable production basin of Mont Saint-Michel (France made with sediments from the bay of Mont Saint-Michel in 2013. Increasing the dose of OM increased soil organic carbon from 10 to 45 g C kg−1 dry soil and increased the porosity and the structural stability, thus decreasing compaction. Increasing the dose of OM also decreased the evaporation rate. VF and DM had similar effects, while those of GWC were weaker. Compared to DM, VF had greater biological stability. Therefore, high OM inputs along with soil decompaction can increase drought resistance by increasing rooting depth and water retention.

Physical and Human Controls on the Carbon Composition of Organic Matter in Tropical Rivers: An Integrated Analysis of Landscape Properties and River Isotopic Composition

Energy Technology Data Exchange (ETDEWEB)

Ballester, M. V.R.; Victoria, R. L.; Krusche, A. V. [Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Piracicaba (Brazil); Bernardes, M. [Universidade Federal Fluminense, Rio de Janeiro (Brazil); Neill, C.; Deegan, L. [Marine Biological Laboratory, Woods Hole, MA (United States); Richey, J. E. [University of Washington, Seatle, WA (United States)

2013-05-15

We applied an integrated analysis of landscape properties including soil properties, land cover and riverine isotopic composition. To evaluate physical and human controls on the carbon composition of organic matter in tropical rivers, we applied an integrated analysis of landscape properties including soil properties, land cover and riverine isotopic composition. Our main objective was to establish the relationship between basin attributes and forms, fluxes and composition of dissolved and particulate organic matter in river channels. A physical template was developed as a GIS-based comprehensive tool to support the understanding of the biogeochemistry of the surface waters of two tropical rivers: the Ji-Parana (Western Amazonia) and the Piracicaba (southeastern of Brazil). For each river we divided the basin into drainage units, organized according to river network morphology and degree of land use impact. Each sector corresponded to a sampling point where river isotopic composition was analysed. River sites and basin characteristics were calculated using datasets compiled as layers in ArcGis Geographical Information System and ERDAS-IMAGINE (Image Processing) software. Each delineated drainage area was individually characterized in terms of topography, soils, river network and land use. Carbon stable isotopic composition of dissolved organic matter (DOM) and particulate organic matter (POM) was determined at several sites along the main tributaries and small streams. The effects of land use on fluvial carbon composition were quantified by a linear regression analysis, relating basin cover and river isotopic composition. The results showed that relatively recent land cover changes have already had an impact on the composition of the riverine DOM and POM, indicating that, as in natural ecosystems, vegetation plays a key role in the composition of riverine organic matter in agricultural ecosystems. (author)

Terrestrial dissolved organic matter distribution in the North Sea.

Science.gov (United States)

Painter, Stuart C; Lapworth, Dan J; Woodward, E Malcolm S; Kroeger, Silke; Evans, Chris D; Mayor, Daniel J; Sanders, Richard J

2018-07-15

The flow of terrestrial carbon to rivers and inland waters is a major term in the global carbon cycle. The organic fraction of this flux may be buried, remineralized or ultimately stored in the deep ocean. The latter can only occur if terrestrial organic carbon can pass through the coastal and estuarine filter, a process of unknown efficiency. Here, data are presented on the spatial distribution of terrestrial fluorescent and chromophoric dissolved organic matter (FDOM and CDOM, respectively) throughout the North Sea, which receives organic matter from multiple distinct sources. We use FDOM and CDOM as proxies for terrestrial dissolved organic matter (tDOM) to test the hypothesis that tDOM is quantitatively transferred through the North Sea to the open North Atlantic Ocean. Excitation emission matrix fluorescence and parallel factor analysis (EEM-PARAFAC) revealed a single terrestrial humic-like class of compounds whose distribution was restricted to the coastal margins and, via an inverse salinity relationship, to major riverine inputs. Two distinct sources of fluorescent humic-like material were observed associated with the combined outflows of the Rhine, Weser and Elbe rivers in the south-eastern North Sea and the Baltic Sea outflow to the eastern central North Sea. The flux of tDOM from the North Sea to the Atlantic Ocean appears insignificant, although tDOM export may occur through Norwegian coastal waters unsampled in our study. Our analysis suggests that the bulk of tDOM exported from the Northwest European and Scandinavian landmasses is buried or remineralized internally, with potential losses to the atmosphere. This interpretation implies that the residence time in estuarine and coastal systems exerts an important control over the fate of tDOM and needs to be considered when evaluating the role of terrestrial carbon losses in the global carbon cycle. Copyright © 2018 The Author(s). Published by Elsevier B.V. All rights reserved.

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)

Measuring organic matter in Everglades wetlands and the Everglades Agricultural Area

Energy Technology Data Exchange (ETDEWEB)

Wright, Alan L. [Univ. of Florida, Gainesville, FL (United States); Hanlon, Edward A. [Univ. of Florida, Gainesville, FL (United States)

2015-01-01

estimate of organic carbon (organic matter) for decisions regarding pesticide applications and estimated contribution of nutrients released from the organic matter in their fields. Restoration efforts in the Everglades wetlands can be better documented with the lower cost, but now equally as useful, LOI test for organic carbon. Improvements to soil organic matter coupled with other measurements of biological health of the system can be documented with less work using the adjusted LOI calculations.

The effect of mixed oxidants and powdered activated carbon on the removal of natural organic matter.

Science.gov (United States)

Alvarez-Uriarte, Jon I; Iriarte-Velasco, Unai; Chimeno-Alanís, Noemí; González-Velasco, Juan R

2010-09-15

Present paper studies the influence of electrochemically generated mixed oxidants on the physicochemical properties of natural organic matter, and especially from the disinfection by-products formation point of view. The study was carried out in a full scale water treatment plant. Results indicate that mixed oxidants favor humic to non-humic conversion of natural organic matter. Primary treatment preferentially removes the more hydrophobic fraction. This converted the non-humic fraction in an important source of disinfection by-products with a 20% contribution to the final trihalomethane formation potential (THMFP(F)) of the finished water. Enhanced coagulation at 40 mg l(-1) of polyaluminium chloride with a moderate mixing intensity (80 rpm) and pH of 6.0 units doubled the removal efficiency of THMFP(F) achieved at full scale plant. However, gel permeation chromatography data revealed that low molecular weight fractions were still hardly removed. Addition of small amounts of powdered activated carbon, 50 mg l(-1), allowed reduction of coagulant dose by 50% whereas removal of THMFP(F) was maintained or even increased. In systems where mixed oxidants are used addition of powdered activated carbon allows complementary benefits by a further reduction in the THMFP(F) compared to the conventional only coagulation-flocculation-settling process. Copyright 2010 Elsevier B.V. All rights reserved.

Organic carbon, nitrogen and phosphorus contents of some tea soils

International Nuclear Information System (INIS)

Ahmed, M.S.; Zamir, M.R.; Sanauallah, A.F.M.

2005-01-01

Soil samples were collected from Rungicherra Tea-Estate of Moulvibazar district, Bangladesh. Organic carbon, organic matter, total nitrogen and available phosphorus content of the collected soil of different topographic positions have been determined. The experimental data have been analyzed statistically and plotted against topography and soil depth. Organic carbon and organic matter content varied from 0.79 to 1.24% and 1.37 to 2.14%. respectively. Total nitrogen and available phosphorus content of these soils varied respectively from 0.095 to 0.13% and 2.31 to 4.02 ppm. (author)

The soil organic carbon content of anthropogenically altered organic soils effects the dissolved organic matter quality, but not the dissolved organic carbon concentrations

Science.gov (United States)

Frank, Stefan; Tiemeyer, Bärbel; Bechtold, Michel; Lücke, Andreas; Bol, Roland

2016-04-01

Dissolved organic carbon (DOC) is an important link between terrestrial and aquatic ecosystems. This is especially true for peatlands which usually show high concentrations of DOC due to the high stocks of soil organic carbon (SOC). Most previous studies found that DOC concentrations in the soil solution depend on the SOC content. Thus, one would expect low DOC concentrations in peatlands which have anthropogenically been altered by mixing with sand. Here, we want to show the effect of SOC and groundwater level on the quantity and quality of the dissolved organic matter (DOM). Three sampling sites were installed in a strongly disturbed bog. Two sites differ in SOC (Site A: 48%, Site B: 9%) but show the same mean annual groundwater level of 15 and 18 cm below ground, respectively. The SOC content of site C (11%) is similar to Site B, but the groundwater level is much lower (-31 cm) than at the other two sites. All sites have a similar depth of the organic horizon (30 cm) and the same land-use (low-intensity sheep grazing). Over two years, the soil solution was sampled bi-weekly in three depths (15, 30 and 60 cm) and three replicates. All samples were analyzed for DOC and selected samples for dissolved organic nitrogen (DON) and delta-13C and delta-15N. Despite differences in SOC and groundwater level, DOC concentrations did not differ significantly (A: 192 ± 62 mg/L, B: 163 ± 55 mg/L and C: 191 ± 97 mg/L). At all sites, DOC concentrations exceed typical values for peatlands by far and emphasize the relevance even of strongly disturbed organic soils for DOC losses. Individual DOC concentrations were controlled by the temperature and the groundwater level over the preceding weeks. Differences in DOM quality were clearer. At site B with a low SOC content, the DOC:DON ratio of the soil solution equals the soil's C:N ratio, but the DOC:DON ratio is much higher than the C:N ratio at site A. In all cases, the DOC:DON ratio strongly correlates with delta-13C. There is no

GRANULOMETRIC AND HUMIC FRACTIONS CARBON STOCKS OF SOIL ORGANIC MATTER UNDER NO-TILLAGE SYSTEM IN UBERABA, BRAZIL

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Marcos Gervasio Pereira

2011-12-01

Full Text Available The cover plant use preceding grain crops in Cerrado soil can increase the carbon stocks of chemical and physical fractions of soil organic matter (SOM. The present study aimed to quantify the carbon stocks of SOM granulometric and humic fractions in a Cerrado area under no-tillage system with different cover plant, and compare the results with those from conventional tillage and fallow areas, in Uberaba, MG, Brazil. The implemented cover crops were: millet, tropical grass and sunn hemp. Furthermore, an area was used in fallow and another as a control area (conventional tillage. After cover crop removal, the areas were subdivided for the corn and soybean plantation. Soil samples were collected in the 0.0-0.025, 0.025-0.05, 0.05-0.10 and 0.10-0.20 m depths, with posterior quantification of total organic carbon (TOC levels and chemical and granulometric fractionation of SOM. Humic acid carbon (C-HAF, fulvic acids (C-FAF and humin (C-HUM were quantified through these fractionations. The granulometric fractions consisted in particulate organic matter (POM and mineral organic matter (MOM. Using the carbon levels for each fraction, the respective stocks for each depth were calculated, including the 0.0-0.20 m layer. In the 0.0-0.20 m layer, TOC had the highest stocks for the millet area. The highest POM stocks were found for the corn plantation over sunn hemp and the fallow and soybean area over millet and tropical grass (0.0-0.20 m. In relation to the MOM stocks, the highest values were observed in the areas with millet, sunn hemp and tropical (palisade grass, all superior to those found in the conventional tillage and fallow areas, independent of evaluated culture (0.10-0.20 m. The highest C-HUM stocks were observed in the area with tropical grass (0.025-0.05 m and areas with tropical grass and sunn hemp (0.10-0.20 m, when compared to conventional tillage, independent of evaluated culture (corn and soybean. The highest C-FAH stocks in the depth of 0

Dynamics of the organic matter from the soil resulting from the changes of the Amazon northeastern ground use

International Nuclear Information System (INIS)

Camargo, Plinio Barbosa de; Martinelli, Luiz Antonio; Victoria, Reynaldo Luiz; Trumbore, Susan

1997-01-01

Aiming a better understanding of the problems related with carbon dynamic in the Amazon soils, soil profiles have been sampled for the determination of: soil carbon content and the variations between areas covered with natural forests, pastures and brush woods; average permanence time of the soil organic matter and the variations between different vegetal covering types; soil organic matter quality in terms of the refractory characteristics and the variation resulting from the changes in the vegetation type. The obtained answers define the soil organic matter dynamic itself. Therefore, the organic matter elementary analysis has been combined, by determining the carbon concentration, with the use of carbon natural isotope 14 C and the stable 13 C

Stable isotopes of bulk organic matter to trace carbon and nitrogen dynamics in an estuarine ecosystem in Babitonga Bay (Santa Catarina, Brazil)

International Nuclear Information System (INIS)

Barros, Grace Virginia; Martinelli, Luiz Antonio; Oliveira Novais, Therezinha M.; Ometto, Jean Pierre H.B.; Zuppi, Gian Maria

2010-01-01

The biogeochemical processes affecting the transport and cycling of terrestrial organic carbon in coastal and transition areas are still not fully understood. One means of distinguishing between the sources of organic materials contributing to particulate organic matter (POM) in Babitonga Bay waters and sediments is by the direct measurement of δ 13 C of dissolved inorganic carbon (DIC) and δ 13 C and δ 15 N in the organic constituents. An isotopic survey was taken from samples collected in the Bay in late spring of 2004. The results indicate that the δ 13 C and δ 15 N compositions of OM varied from - 21.7 per mille to - 26.2 per mille and from + 9.2 per mille to - 0.1 per mille , respectively. δ 13 C from DIC ranges from + 0.04 per mille to - 12.7 per mille . The difference in the isotope compositions enables the determination of three distinct end-members: terrestrial, marine and urban. Moreover, the evaluation of source contribution to the particulate organic matter (POM) in the Bay, enables assessment of the anthropogenic impact. Comparing the depleted values of δ 13 C DIC and δ 13 C POC it is possible to further understand the carbon dynamic within Babitonga Bay.

Impact of biological activated carbon pre-treatment on the hydrophilic fraction of effluent organic matter for mitigating fouling in microfiltration.

Science.gov (United States)

Pramanik, Biplob Kumar; Roddick, Felicity A; Fan, Linhua

2017-07-24

The hydrophilic (HPI) fraction of effluent organic matter, which has protein and carbohydrate contents, has a high propensity to foul low-pressure membranes. Biological activated carbon (BAC) filtration was examined as a pre-treatment for reducing the fouling of a microfiltration (MF) membrane (0.1 µm PVDF) by the HPI organic fraction extracted from a biologically treated secondary effluent (BTSE). Although the BAC removed less dissolved organic carbon, carbohydrate and protein from the HPI fraction than the granular activated carbon treatment which was used for comparison, it led to better improvement in permeate flux. This was shown to be due to the removal/breakdown of the HPI fraction resulting in less deposition of these organics on the membrane, many components of which are high molecular weight biopolymers (such as protein and carbohydrate molecules) through biodegradation and adsorption of those molecules on the biofilm and activated carbon. This study established the potential of BAC pre-treatment for reducing the HPI fouling of the membrane and thus improving the performance for the MF of BTSE for water reclamation.

Chemical attributes, total organic carbon stock and humified fractions of organic matter soil submitted to different systems of sugarcane management

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Jean Sérgio Rosset

2014-10-01

Full Text Available Mechanized harvesting maintenance of trash from cane sugar and soil application of waste as vinasse and filter cake can improve the system of crop yield. Thus, this study aimed to evaluate the changes in the chemical, the stock of total organic carbon and humified organic matter fractions in an Oxisol cultivated with cane sugar with the following management systems: with sugarcane vinasse application (CCV, without application of burnt cane waste (CQS, with burnt cane vinasse application (CQV, with application of burnt cane filter cake (CQTF and burnt cane with joint application of vinasse and filter cake (CQVTF. For reference we used an area of natural vegetation (NV, Cerrado sensu stricto. Treatment CQVTF showed improvement in soil chemical properties, increased inventory levels of total organic carbon – TOC (values ranging from 21.28 to 40.02 Mg ha-1 and humified fractions of soil organic matter in relation to other treatments. The CQS area at a depth of 0-0.05 m, showed the greatest losses of soil TOC stocks (56.3% compared to NV. The adoption of management presented CCV and chemical attributes of the soil TOC stocks equivalent to those observed in areas with CQV CQTF and despite the short period of adoption (3 years. The TOC correlated with the sum of bases (r = 0.76 **, cation exchange capacity (r = 0.59 ** and base saturation (r = 0.63 **, while the humic acids (r = 0.40 ** fulvic acids (r = 0.49 ** and humin (r = 0.59 ** correlated with the cation exchange capacity of the soil. These results indicate that the preservation of trash in the management of cane sugar added to the application of vinasse and filter cake increases the TOC stocks promoting improvement in soil chemical properties.

Characterization of Natural Organic Matter by FeCl3 Coagulation

Science.gov (United States)

Cahyonugroho, O. H.; Hidayah, E. N.

2018-01-01

Natural organic matter (NOM) is heterogenous mixture of organic compounds that enter the water from various decomposition and metabolic reactions, including animal, plant, domestic and industrial wastes. NOM refers to group of carbon-based compounds that are found in surface water and ground water. The aim of the study is to assess organic matter characteristics in Jagir River as drinking water source and to characterize the organic components that could be removed during coagulation. Coagulation is the common water treatment process can be used to remove NOM with FeCl3 coagulant in various dosage. NOM surrogates, including total organic carbon (TOC), ultraviolet absorbance at 254 nm (UV254) and specific UV absorbance (SUVA) were chosen to assess the organic removal. Results of jar test experiments showed that NOM can be removed about 40% of NOM surrogates with 200 mg/L FeCl3. About 60% removal of total organic fraction, which is mainly humic substances, as detected by size exclusion chromatography (SEC).

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

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

NARCIS (Netherlands)

Karlsson, E. S.; Charkin, A. N.; Dudarev, O.; Semiletov, I.; Vonk, J. E.; Sánchez-García, L.; Andersson, A.

2011-01-01

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

Carbon sequestration in soil by in situ catalyzed photo-oxidative polymerization of soil organic matter.

Science.gov (United States)

Piccolo, Alessandro; Spaccini, Riccardo; Nebbioso, Antonio; Mazzei, Pierluigi

2011-08-01

Here we describe an innovative mechanism for carbon sequestration in soil by in situ photopolymerization of soil organic matter under biomimetic catalysis. Three different Mediterranean soils were added with a synthetic water-soluble iron-porphyrin, irradiated by solar light, and subjected first to 5 days incubation and, then, 15, and 30 wetting and drying (w/d) cycles. The in situ catalyst-assisted photopolymerization of soil organic carbon (SOC) increased water stability of soil aggregates both after 5 days incubation and 15 w/d cycles, but not after 30 w/d cycles. Particle-size distribution of all treated soils confirmed the induced soil physical improvement, by showing a concomitant lower yield of the clay-sized fraction and larger yields of either coarse sand- or fine sand-size fractions, depending on soil texture, though only after 5 days incubation. The gain in soil physical quality was reflected by the shift of OC content from small to large soil aggregates, thereby suggesting that photopolymerization stabilized OC by both chemical and physical processes. A further evidence of the carbon sequestration capacity of the photocatalytic treatment was provided by the significant reduction of CO(2) respired by all soils after both incubation and w/d cycles. Our findings suggest that "green" catalytic technologies may potentially be the bases for future practices to increase soil carbon stabilization and mitigate CO(2) emissions from arable soils.

Determining the spatial variability of wetland soil bulk density, organic matter, and the conversion factor between organic matter and organic carbon across coastal Louisiana, U.S.A.

Science.gov (United States)

Wang, Hongqing; Piazza, Sarai C.; Sharp, Leigh A.; Stagg, Camille L.; Couvillion, Brady R.; Steyer, Gregory D.; McGinnis, Thomas E.

2016-01-01

Soil bulk density (BD), soil organic matter (SOM) content, and a conversion factor between SOM and soil organic carbon (SOC) are often used in estimating SOC sequestration and storage. Spatial variability in BD, SOM, and the SOM–SOC conversion factor affects the ability to accurately estimate SOC sequestration, storage, and the benefits (e.g., land building area and vertical accretion) associated with wetland restoration efforts, such as marsh creation and sediment diversions. There are, however, only a few studies that have examined large-scale spatial variability in BD, SOM, and SOM–SOC conversion factors in coastal wetlands. In this study, soil cores, distributed across the entire coastal Louisiana (approximately 14,667 km2) were used to examine the regional-scale spatial variability in BD, SOM, and the SOM–SOC conversion factor. Soil cores for BD and SOM analyses were collected during 2006–09 from 331 spatially well-distributed sites in the Coastwide Reference Monitoring System network. Soil cores for the SOM–SOC conversion factor analysis were collected from 15 sites across coastal Louisiana during 2006–07. Results of a split-plot analysis of variance with incomplete block design indicated that BD and SOM varied significantly at a landscape level, defined by both hydrologic basins and vegetation types. Vertically, BD and SOM varied significantly among different vegetation types. The SOM–SOC conversion factor also varied significantly at the landscape level. This study provides critical information for the assessment of the role of coastal wetlands in large regional carbon budgets and the estimation of carbon credits from coastal restoration.

Organic carbon production, mineralisation and preservation on the Peruvian margin

Science.gov (United States)

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

2015-03-01

Carbon cycling in Peruvian margin sediments (11 and 12° S) was examined at 16 stations, from 74 m water depth on the middle shelf down to 1024 m, using a combination of in situ flux measurements, sedimentary geochemistry and modelling. Bottom water oxygen was below detection limit down to ca. 400 m and increased to 53 μM at the deepest station. Sediment accumulation rates decreased sharply seaward of the middle shelf and subsequently increased at the deep stations. The organic carbon burial efficiency (CBE) was unusually low on the middle shelf (60%) at the deep oxygenated sites. In line with other studies, CBE was elevated under oxygen-deficient waters in the mid-water oxygen minimum zone. Organic carbon rain rates calculated from the benthic fluxes alluded to efficient mineralisation of organic matter in the water column compared to other oxygen-deficient environments. The observations at the Peruvian margin suggest that a lack of oxygen does not greatly affect the degradation of organic matter in the water column but promotes the preservation of organic matter in sediments.

Organic and Inorganic Matter in Louisiana Coastal Waters: Vermilion, Atchafalaya, Terrebonne, Barataria, and Mississippi Regions.

Science.gov (United States)

Chromophoric dissolved organic matter (CDOM) spectral absorption, dissolved organic carbon (DOC) concentration, and the particulate fraction of inorganic (PIM) and organic matter (POM) were measured in Louisiana coastal waters at Vermilion, Atchafalaya, Terrebonne, Barataria, and...

Seafloor ecosystem functioning: the importance of organic matter priming

NARCIS (Netherlands)

Van Nugteren, P.; Moodley, L.; Brummer, G.J.; Heip, C.H.R.; Herman, P.M.J.; Middelburg, J.J.

2009-01-01

Organic matter (OM) remineralization may be considered a key function of the benthic compartment of marine ecosystems and in this study we investigated if the input of labile organic carbon alters mineralization of indigenous sediment OM (OM priming). Using 13C-enriched diatoms as labile tracer

Mean residence time of soil organic matter associated with kaolinite and smectite

NARCIS (Netherlands)

Wattel-Koekkoek, E.J.W.; Buurman, P.; Plicht, van der J.; Wattel, J.T.; Breemen, van N.

2003-01-01

To gain insight into the effect of clay mineralogy on the turnover of organic matter, we analysed the C-14 activity of soil organic matter associated with clay in soils dominated by kaolinite and smectite in natural savanna systems in seven countries. Assuming that carbon inputs and outputs are in

Mean residence time of soil organic matter associated with kaolinite and smectite

NARCIS (Netherlands)

Wattel-Koekkoek, E.J.W.; Buurman, P.; Plicht, J. van der; Wattel, E.; Breemen, N. van

To gain insight into the effect of clay mineralogy on the turnover of organic matter, we analysed the C-14 activity of soil organic matter associated with clay in soils dominated by kaolinite and smectite in natural savanna systems in seven countries. Assuming that carbon inputs and outputs are in

Separating the effects of organic matter-mineral interactions and organic matter chemistry on the sorption of diuron and phenanthrene.

Science.gov (United States)

Ahangar, Ahmad Gholamalizadeh; Smernik, Ronald J; Kookana, Rai S; Chittleborough, David J

2008-06-01

Even though it is well established that soil C content is the primary determinant of the sorption affinity of soils for non-ionic compounds, it is also clear that organic carbon-normalized sorption coefficients (K(OC)) vary considerably between soils. Two factors that may contribute to K(OC) variability are variations in organic matter chemistry between soils and interactions between organic matter and soil minerals. Here, we quantify these effects for two non-ionic sorbates-diuron and phenanthrene. The effect of organic matter-mineral interactions were evaluated by comparing K(OC) for demineralized (HF-treated) soils, with K(OC) for the corresponding whole soils. For diuron and phenanthrene, average ratios of K(OC) of the HF-treated soils to K(OC) of the whole soils were 2.5 and 2.3, respectively, indicating a substantial depression of K(OC) due to the presence of minerals in the whole soils. The effect of organic matter chemistry was determined by correlating K(OC) against distributions of C types determined using solid-state (13)C NMR spectroscopy. For diuron, K(OC) was positively correlated with aryl C and negatively correlated with O-alkyl C, for both whole and HF-treated soils, whereas for phenanthrene, these correlations were only present for the HF-treated soils. We suggest that the lack of a clear effect of organic matter chemistry on whole soil K(OC) for phenanthrene is due to an over-riding influence of organic matter-mineral interactions in this case. This hypothesis is supported by a correlation between the increase in K(OC) on HF-treatment and the soil clay content for phenanthrene, but not for diuron.

Calcium and organic matter removal by carbonation process with waste incineration flue gas towards improvement of leachate biotreatment performance.

Science.gov (United States)

Zhang, Cheng; Zhu, Xuedong; Wu, Liang; Li, Qingtao; Liu, Jianyong; Qian, Guangren

2017-09-01

Municipal solid wastes incineration (MSWI) flue gas was employed as the carbon source for in-situ calcium removal from MSWI leachate. Calcium removal efficiency was 95-97% with pH of 10.0-11.0 over 100min of flue gas aeration, with both bound Ca and free Ca being removed effectively. The fluorescence intensity of tryptophan, protein-like and humic acid-like compounds increased after carbonation process. The decrease of bound Ca with the increase of precipitate indicated that calcium was mainly converted to calcium carbonate precipitate. It suggested that the interaction between dissolved organic matter and Ca 2+ was weakened. Moreover, 10-16% of chemical oxygen demand removal and the decrease of ultraviolet absorption at 254nm indicated that some organics, especially aromatic compound decreased via adsorption onto the surface of calcium carbonate. The results indicate that introduce of waste incineration flue gas could be a feasible way for calcium removal from leachate. Copyright © 2017 Elsevier Ltd. All rights reserved.

Modeling the vertical soil organic matter profile using Bayesian parameter estimation

Directory of Open Access Journals (Sweden)

M. C. Braakhekke

2013-01-01

Full Text Available The vertical distribution of soil organic matter (SOM in the profile may constitute an important factor for soil carbon cycling. However, the formation of the SOM profile is currently poorly understood due to equifinality, caused by the entanglement of several processes: input from roots, mixing due to bioturbation, and organic matter leaching. In this study we quantified the contribution of these three processes using Bayesian parameter estimation for the mechanistic SOM profile model SOMPROF. Based on organic carbon measurements, 13 parameters related to decomposition and transport of organic matter were estimated for two temperate forest soils: an Arenosol with a mor humus form (Loobos, the Netherlands, and a Cambisol with mull-type humus (Hainich, Germany. Furthermore, the use of the radioisotope ²¹⁰Pb_ex as tracer for vertical SOM transport was studied. For Loobos, the calibration results demonstrate the importance of organic matter transport with the liquid phase for shaping the vertical SOM profile, while the effects of bioturbation are generally negligible. These results are in good agreement with expectations given in situ conditions. For Hainich, the calibration offered three distinct explanations for the observations (three modes in the posterior distribution. With the addition of ²¹⁰Pb_ex data and prior knowledge, as well as additional information about in situ conditions, we were able to identify the most likely explanation, which indicated that root litter input is a dominant process for the SOM profile. For both sites the organic matter appears to comprise mainly adsorbed but potentially leachable material, pointing to the importance of organo-mineral interactions. Furthermore, organic matter in the mineral soil appears to be mainly derived from root litter, supporting previous studies that highlighted the importance of root input for soil carbon sequestration. The ²¹⁰

Can Biochar Protect Labile Organic Matter Against Mineralization in Soil?

Institute of Scientific and Technical Information of China (English)

Giovanna B.MELAS; Oriol ORTIZ; Josep M.ALACA(N)IZ

2017-01-01

Biochar could help to stabilize soil organic (SOM) matter,thus sequestering carbon (C) into the soil.The aim of this work was to determine an easy method i) to estimate the effects of the addition of biochar and nutrients on the organic matter (SOM)mineralization in an artificial soil,proposed by the Organization for Economic Co-operation and Development (OECD),amended with glucose and ii) to measure the amount of labile organic matter (glucose) that can be sorbed and thus be partially protected in the same soil,amended or not amended with biochar.A factorial experiment was designed to check the effects of three single factors (biochar,nutrients,and glucose) and their interactions on whole SOM mineralization.Soil samples were inoculated with a microbial inoculum and preincubated to ensure that their biological activities were not limited by a small amount of microbial biomass,and then they were incubated in the dark at 21 ℃ for 619 d.Periodical measurements of C mineralized to carbon dioxide (CO2) were carried out throughout the 619-d incubation to allow the mineralization of both active and slow organic matter pools.The amount of sorbed glucose was calculated as the difference between the total and remaining amounts of glucose added in a soil extract.Two different models,the Freundlich and Langmuir models,were selected to assess the equilibrium isotherms of glucose sorption.The CO2-C release strongly depended on the presence of nutrients only when no biochar was added to the soil.The mineralization of organic matter in the soil amended with both biochar and glucose was equal to the sum of the mineralization of the two C sources separately.Furthermore,a significant amount of glucose can be sorbed on the biochar-amended soil,suggesting the involvement of physico-chemical mechanisms in labile organic matter protection.

Peatland Organic Matter Chemistry Trends Over a Global Latitudinal Gradient

Science.gov (United States)

Verbeke, B. A.; Hodgkins, S. B.; Carson, M. A.; Lamit, L. J.; Lilleskov, E.; Chanton, J.

2017-12-01

Peatlands contain a significant amount of the global soil carbon, and the climate feedback of carbon cycling within these peatland systems is still relatively unknown. Organic matter composition of peatlands plays a major role in determining carbon storage, and while high latitude peatlands seem to be the most sensitive to climate change, a global picture of peat organic matter chemistry is required to improve predictions and models of greenhouse gas emissions fueled by peatland decomposition. The objective of this research is to test the hypothesis that carbohydrate content of peatlands near the equator will be lower than high latitude peatlands, while aromatic content will be higher. As a part of the Global Peatland Microbiome Project (GPMP), around 2000 samples of peat from 10 to 70 cm across a latitudinal gradient of 79 N to 53 S were measured with Fourier transform infrared spectroscopy (FTIR) to examine the organic matter functional groups of peat. Carbohydrate and aromatic content, as determined by FTIR, are useful proxies of decomposition potential and recalcitrance, respectively. We found a highly significant relationship between carbohydrate and aromatic content, latitude, and depth. Carbohydrate content of high latitude sites were significantly greater than at sites near the equator, in contrast to aromatic content which showed the opposite trend. It is also clear that carbohydrate content decreases with depth while aromatic content increases with depth. Higher carbohydrate content at higher latitudes indicates a greater potential for lability and resultant mineralization to form the greenhouse gases, carbon dioxide and methane, whereas the composition of low latitude peatlands is consistent with their apparent stability. We speculate that the combination of low carbohydrates and high aromatics at warmer locations near the equator could foreshadow the organic matter composition of high latitude peat transitioning to a more recalcitrant form with a

Organic matter degradation in Chilean sediments - following nature's own degradation experiment

DEFF Research Database (Denmark)

Langerhuus, Alice Thoft; Niggemann, Jutta; Lomstein, Bente Aagaard

ORGANIC MATTER DEGRADATION IN CHILEAN SEDIMENTS – FOLLOWING NATURE’S OWN DEGRADATION EXPERIMENT Degradation of sedimentary organic matter was studied at two stations from the shelf of the Chilean upwelling region. Sediment cores were taken at 1200 m and 800 m water depth and were 4.5 m and 7.5 m...... in length, respectively. The objective of this study was to assess the degradability of the organic matter from the sediment surface to the deep sediments. This was done by analysing amino acids (both L- and D-isomers) and amino sugars in the sediment cores, covering a timescale of 15.000 years. Diagenetic...... indicators (percentage of carbon and nitrogen present as amino acid carbon and nitrogen, the ratio between a protein precursor and its non-protein degradation product and the percentage of D-amino acids) revealed ongoing degradation in these sediments, indicating that microorganisms were still active in 15...

Assessment of the unidentified organic matter fraction in fogwater using fluorescence spectroscopy

Science.gov (United States)

Valsaraj, K.; Birdwell, J.

2010-07-01

Dissolved organic matter (DOM) in fogwaters from southeastern Louisiana and central-eastern China has been characterized using excitation-emission matrix (EEM) fluorescence spectroscopy. The results demonstrate that fluorescence spectroscopy can be used to obtain a qualitative assessment of the large fraction of fogwater organic carbon (~40 - 80% by weight) that cannot be identified in terms of specific chemical compounds. The method has the principle advantage that it can be applied at natural abundance concentrations, thus eliminating the need for large sample volumes required to isolate DOM for characterization by other spectroscopic (NMR, FTIR) and chemical (elemental) analyses. It was anticipated that the fogwater organic matter fluorescence spectra would resemble those of surface and rain waters, containing peaks indicative of both humic substances and fluorescent amino acids. Humic- and protein-like fluorophores were observed in the fogwater spectra and fluorescence-derived indices had values comparable to other natural waters. Biological character (intensity of tyrosine and tryptophan peaks) was found to increase with organic carbon concentration. Fogwater organic matter appears to contain a mixture of terrestrially- and microbially-derived material. The fluorescence results show that most of the unidentified fogwater organic carbon can be represented by humic-like and biologically-derived substances similar to those present in other aquatic systems.

Vertical transport of organic matter in the various oceanic areas

International Nuclear Information System (INIS)

Handa, Nobuhiko; Hayakawa, Kazuhide

1993-01-01

Organic matter produced by the photosynthesis of the phytoplankton is removed from the euphotic layer to the underlying waters by sinking of the particles consisting of both marine snow and fecal pellet. Phytoplankton bloom always enhances the vertical flux of organic matter from the subsurface to deep waters. Turbidity current is another factor to govern the vertical flux of organic carbon especially in the continental shelf to its slope areas. However, no information are available to distinguish the organic materials from these two sources. Stable carbon isotope ratio and fatty acid composition give most promising informations to diagnose the physiological state of the phytoplankton which is one of the source of the organic materials of the sinking particle, because of the extensive variations of the δ 13 C of the phytoplankton cellular organic matter and fatty acid composition due to the phytoplankton growth rate (O'Leary, 1981; Morris et al., 1985). Δ 14 C of the organic matter of the sinking particle will provide an information as to how much organic materials are derived from the phytoplankton growing in the surface and subsurface waters and/or from the resuspended particles of the surface sediment in the continental shelf and its slope areas. Recently we analyzed various samples of the sinking particles collected from the coastal areas of the Antarctica and off Hokkaido, Japan for fatty acids and found that ratios as biomarker to diagnose these growth phases of the phytoplankton growing in the surface to subsurface waters. Thus, we intend to report here these data obtained. (J.P.N.)

Organic carbon, nitrogen and phosphorus contents of some soils of kaliti tea-estate, Bangladesh

International Nuclear Information System (INIS)

Ahmed, M. S.; Shahin, M. M. H.; Sanaullah, A. F. M.

2005-01-01

Some soil samples were collected from Kaliti Tea-Estate of Moulvibazar district, Bangladesh. Total nitrogen, organic carbon, organic matter, carbon-nitrogen ratio and available phosphorus content of the collected soil samples of different depths and of different topographic positions have been determined. Total nitrogen was found 0.07 to 0.12 % organic carbon and organic matter content found to vary from 0.79 to 1.25 and 1.36 to 2.15 % respectively. Carbon-nitrogen ratio of these soils varied from 9.84 to 10.69, while available phosphorus content varied from 2.11 to 4.13 ppm. (author)

Relationships between colored dissolved organic matter and dissolved organic carbon in different coastal gradients of the Baltic Sea.

Science.gov (United States)

Harvey, E Therese; Kratzer, Susanne; Andersson, Agneta

2015-06-01

Due to high terrestrial runoff, the Baltic Sea is rich in dissolved organic carbon (DOC), the light-absorbing fraction of which is referred to as colored dissolved organic matter (CDOM). Inputs of DOC and CDOM are predicted to increase with climate change, affecting coastal ecosystems. We found that the relationships between DOC, CDOM, salinity, and Secchi depth all differed between the two coastal areas studied; the W Gulf of Bothnia with high terrestrial input and the NW Baltic Proper with relatively little terrestrial input. The CDOM:DOC ratio was higher in the Gulf of Bothnia, where CDOM had a greater influence on the Secchi depth, which is used as an indicator of eutrophication and hence important for Baltic Sea management. Based on the results of this study, we recommend regular CDOM measurements in monitoring programmes, to increase the value of concurrent Secchi depth measurements.

Radiocarbon dating of fluvial organic matter reveals land-use impacts in boreal peatlands

DEFF Research Database (Denmark)

Hulatt, Chris J.; Kaartokallio, Hermanni; Oinonen, Markku

2014-01-01

This study measured the effects of land use on organic matter released to surface waters in a boreal peat catchment using radiocarbon dating of particulate and dissolved organic carbon (POC and DOC), DOC concentration, stable carbon and nitrogen isotope composition, and optical measurements. Undi...

Fossil organic matter characteristics in permafrost deposits of the northeast Siberian Arctic

Science.gov (United States)

Lutz Schirrmeister; Guido Grosse; Sebastian Wetterich; Pier Paul Overduin; Jens Straub; Edward A.G. Schuur; Hans-Wolfgang. Hubberton

2011-01-01

Permafrost deposits constitute a large organic carbon pool highly vulnerable to degradation and potential carbon release due to global warming. Permafrost sections along coastal and river bank exposures in NE Siberia were studied for organic matter (OM) characteristics and ice content. OM stored in Quaternary permafrost grew, accumulated, froze, partly decomposed, and...

Stabilization of dissolved organic matter by aluminium: A toxic effect or stabilization through precipitation?

NARCIS (Netherlands)

Scheel, T.; Jansen, B.; van Wijk, A.J.; Verstraten, J.M.; Kalbitz, K.

2008-01-01

Carbon mineralization in acidic forest soils can be retarded by large concentrations of aluminium (Al). However, it is still unclear whether Al reduces C mineralization by direct toxicity to microorganisms or by decreased bioavailability of organic matter (OM) because dissolved organic matter (DOM)

Storage and turnover of organic matter in soil

Energy Technology Data Exchange (ETDEWEB)

Torn, M.S.; Swanston, C.W.; Castanha, C.; Trumbore, S.E.

2008-07-15

Historically, attention on soil organic matter (SOM) has focused on the central role that it plays in ecosystem fertility and soil properties, but in the past two decades the role of soil organic carbon in moderating atmospheric CO{sub 2} concentrations has emerged as a critical research area. This chapter will focus on the storage and turnover of natural organic matter in soil (SOM), in the context of the global carbon cycle. Organic matter in soils is the largest carbon reservoir in rapid exchange with atmospheric CO{sub 2}, and is thus important as a potential source and sink of greenhouse gases over time scales of human concern (Fischlin and Gyalistras 1997). SOM is also an important human resource under active management in agricultural and range lands worldwide. Questions driving present research on the soil C cycle include: Are soils now acting as a net source or sink of carbon to the atmosphere? What role will soils play as a natural modulator or amplifier of climatic warming? How is C stabilized and sequestered, and what are effective management techniques to foster these processes? Answering these questions will require a mechanistic understanding of how and where C is stored in soils. The quantity and composition of organic matter in soil reflect the long-term balance between plant carbon inputs and microbial decomposition, as well as other loss processes such as fire, erosion, and leaching. The processes driving soil carbon storage and turnover are complex and involve influences at molecular to global scales. Moreover, the relative importance of these processes varies according to the temporal and spatial scales being considered; a process that is important at the regional scale may not be critical at the pedon scale. At the regional scale, SOM cycling is influenced by factors such as climate and parent material, which affect plant productivity and soil development. More locally, factors such as plant tissue quality and soil mineralogy affect

The role of clay minerals in the preservation of organic matter in sediments of Qinghai Lake, NW China

Science.gov (United States)

Yu, Bingsong; Dong, Hailiang; Jiang, Hongchen; Lv, Guo; Eberl, Dennis D.; Li, Shanying; Kim, Jinwook

2009-01-01

The role of saline lake sediments in preserving organic matter has long been recognized. In order to further understand the preservation mechanisms, the role of clay minerals was studied. Three sediment cores, 25, 57, and 500 cm long, were collected from Qinghai Lake, NW China, and dissected into multiple subsamples. Multiple techniques were employed, including density fractionation, X-ray diffraction, scanning and transmission electron microscopy (SEM and TEM), total organic carbon (TOC) and carbon compound analyses, and surface area determination. The sediments were oxic near the water-sediment interface, but became anoxic at depth. The clay mineral content was as much as 36.8%, consisting mostly of illite, chlorite, and halloysite. The TEM observations revealed that organic matter occurred primarily as organic matter-clay mineral aggregates. The TOC and clay mineral abundances are greatest in the mid-density fraction, with a positive correlation between the TOC and mineral surface area. The TOC of the bulk sediments ranges from 1 to 3% with the non-hydrocarbon fraction being predominant, followed by bitumen, saturated hydrocarbon, aromatic hydrocarbons, and chloroform-soluble bitumen. The bimodal distribution of carbon compounds of the saturated hydrocarbon fraction suggests that organic matter in the sediments was derived from two sources: terrestrial plants and microorganisms/algae. Depthrelated systematic changes in the distribution patterns of the carbon compounds suggest that the oxidizing conditions and microbial abundance near the water-sediment interface promote degradation of labile organic matter, probably in adsorbed form. The reducing conditions and small microbial biomass deeper in the sediments favor preservation of organic matter, because of the less labile nature of organic matter, probably occurring within clay mineral-organic matter aggregates that are inaccessible to microorganisms. These results have important implications for our

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: �

Pore water geochemistry and the oxidation of sedimentary organic matter: Hatteras Abyssal Plain 1981

International Nuclear Information System (INIS)

Heggie, D.; Lewis, T.; Graham, D.

1985-01-01

This report presents the pore water geochemistry from R/V an Endeavor cruise to an area of the Hatteras Abyssal Plain between 31 0 45' - 34 0 00'N and 69 0 37.5 - 72 0 07.5'W. The authors report on the down core variations of the products of organic matter oxidation, the stoichiometry of reactions and make a preliminary assessment of the rates of organic matter oxidation at several core locations. The authors found concentrations of total inorganic nitrogen species; nitrate, nitrite and ammonia in pore waters to be less than those predicted from a model of organic matter oxidation (Froelich et al. 1979) in sediments. The observations indicate that nitrogen is depleted over carbon as compared to typical marine organic matter. The down-core nitrate profiles over the study area were used to infer depths at which oxygen is near totally consumed in the sediments and hence to compute rates of oxygen consumption. The authors found oxygen consumption rates to vary by nearly an order of magnitude between core locations (1.7 - >15μmO 2 cm -2 yr -1 ). A simple model which combines the computed rates of oxidant consumption and the stoichiometry of organic matter oxidation was used to make estimates of organic carbon oxidation rates. These latter were found to vary between 1.3 and > 11.5 μm C cm -2 yr -1 . Highest carbon oxidation rates were found at the western boundary of the study area, and in all cases oxygen consumption was responsible for >85% of carbon oxidized. 11 references, 5 figures, 4 tables

Dissolved organic matter (DOM) in microalgal photobioreactors: a potential loss in solar energy conversion?

Science.gov (United States)

Hulatt, Chris J; Thomas, David N

2010-11-01

Microalgae are considered to be a potential alternative to terrestrial crops for bio-energy production due to their relatively high productivity per unit area of land. In this work we examined the amount of dissolved organic matter exuded by algal cells cultured in photobioreactors, to examine whether a significant fraction of the photoassimilated biomass could potentially be lost from the harvestable biomass. We found that the mean maximum amount of dissolved organic carbon (DOC) released measured 6.4% and 17.3% of the total organic carbon in cultures of Chlorellavulgaris and Dunaliella tertiolecta, respectively. This DOM in turn supported a significant growth of bacterial biomass, representing a further loss of the algal assimilated carbon. The release of these levels of DOC indicates that a significant fraction of the photosynthetically fixed organic matter could be lost into the surrounding water, suggesting that the actual biomass yield per hectare for industrial purposes could be somewhat less than expected. A simple and inexpensive optical technique, based on chromophoric dissolved organic matter (CDOM) measurements, to monitor such losses in commercial PBRs is discussed.

Long-term changes in organic matter of woodland soils cleared for arable cropping in Zimbabwe

NARCIS (Netherlands)

Zingore, S.; Manyame, C.; Nyamugafata, P.; Giller, K.E.

2005-01-01

Subsistence farmers in Africa depend largely on the soil organic matter to sustain crop productivity. Long-term changes in soil organic carbon and nitrogen were measured after woodland clearance for smallholder subsistence farming or for commercial farming. The contents of organic carbon and

Changes in different organic matter fractions during conventional treatment and advanced treatment

Institute of Scientific and Technical Information of China (English)

Chao Chen; Xiaojian Zhang; Lingxia Zhu; Wenjie He; Hongda Han

2011-01-01

XAD-8 resin isolation of organic matter in water was used to divide organic matter into the hydrophobic and hydrophilic fractions.A pilot plant was used to investigate the change in both fractions during conventional and advanced treatment processes.The treatment of hydrophobic organics (HPO), rather than hydrophilic organicas (HPI), should carry greater emphasis due to HPO's higher trihalomethane formation potential (THMFP) and haloacetic acid formation potential (HAAFP).The removal of hydrophobic matter and its transmission into hydrophilic matter reduced ultimate DBP yield during the disinfection process.The results showed that sand filtration, ozonation, and biological activated carbon (BAC) filtration had distinct influences on the removal of both organic fractions.Additionally, the combination of processes changed the organic fraction proportions present during treatment.The use of ozonation and BAC maximized organic matter removal efficiency, especially for the hydrophobic fraction.In sum, the combination of pre-ozonation,conventional treatment, and O3-BAC removed 48％ of dissolved organic carbon (DOC), 60％ of HPO, 30％ of HPI, 63％ of THMFP,and 85％ of HAAFP.The use of conventional treatment and O3-BAC without pre-ozonation had a comparable performance, removing 51％ of DOC, 56％ of HPO, 45％ of HPI, 61％ of THMFP, and 72％ of HAAFP.The effectiveness of this analysis method indicated that resin isolation and fractionation should be standardized as an applicable test to help assess water treatment process efficiency.

Investigation of vertical distribution and morphology of indigenous organic matter at Sleeping Bear site, Michigan

Science.gov (United States)

West, C. C.; Lyon, W. G.; Ross, D. L.; Pennington, L. K.

1994-11-01

This study evaluates the nature and origin of particulate organic carbon and organic coatings on aquifer sands upgradient from a fuel spill site near the Sleeping Bear Dunes National Lakeshore in Michigan. The distribution of carbon was found to be highly complex due to the occurrence of high organic carbon horizons, bounded above and below by high carbonate sediments. The organic coatings on the sands were examined using white light and fluorescence microscopy and by scanning electron microscopy. Core samples were analyzed for organic and inorganic carbon, solution pH, humic/fulvic acid ratios, and insoluble organic matter content (that is, humin) as a function of depth from the ground surface. The organic geochemistry of the soil profile at this site was found to be significantly influenced by the carbonates producing a sharp boundary of precipitated organic matter. This boundary was followed by coatings of predominantly fulvic acid salts on mineral grains deeper in the soil column. The coatings extended into the aquifer. The existence of native organic films on sand grains is well documented in the soils literature. The study reported here was greatly aided by this information and provides the framework for future studies concerning the influence of carbon distribution, chemical identity, and morphology on contaminant fate and transport processes.

Organic matter iron and nutrient transport and nature of dissolved organic matter in the drainage basin of a boreal humic river in northern Finland

International Nuclear Information System (INIS)

Heikkinen, K.

1994-01-01

Organic carbon and iron transport into the Gulf of Bothnia and the seasonal changes in the nature of dissolved organic matter (DOM) were studied in 1983 and 1984 at the mouth of the River Kiiminkijoki, which crosses an area of minerotrophic mires in northern Finland. Organic and inorganic transport within the drainage basin was studied in the summer and autumn of 1985 and 1986. The results indicate that the dissolved organic carbon (DOC) is mainly of terrestrial origin, leaching mostly from peatlands. The DOC concentrations decrease under low flow conditions. The proportion of drifting algae as a particulate organic carbon (POC) source seems to increase in summer. The changes in the ratio of Fe/DOC, the colour of the DOM and the ratio of Fe/DOC, the colour of the DOM and the ratio of fluorescence to DOC with discharge give indications of the origin, formation, nature and fate of the DOM in the river water. Temperature-dependent microbiological processes in the formation and sedimentation of Fe-organic colloids seem to be important. Estimates are given for the amounts and transport rates of organic carbon and Fe discharged into the Gulf of Bothnia by river. High apparent molecular weight (HAMW) organic colloids are important for the organic, Fe and P transport in the basin. The DOM in the water consists mainly of fulvic acids, although humic acids are also important. The results indicate an increase in the mobilization of HAMW Fe-organic colloids in the peatlands following drainage and peat mining. The transport of inorganic nitrogen from the peatlands in the area and in the river is increasing due to peat mining. The changes in the transport of organic matter, Fe and P are less marked

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.

Utilizing chromophoric dissolved organic matter measurements to derive export and reactivity of dissolved organic carbon exported to the Arctic Ocean: A case study of the Yukon River, Alaska

Science.gov (United States)

Spencer, R.G.M.; Aiken, G.R.; Butler, K.D.; Dornblaser, M.M.; Striegl, Robert G.; Hernes, P.J.

2009-01-01

The quality and quantity of dissolved organic matter (DOM) exported by Arctic rivers is known to vary with hydrology and this exported material plays a fundamental role in the biogeochemical cycling of carbon at high latitudes. We highlight the potential of optical measurements to examine DOM quality across the hydrograph in Arctic rivers. Furthermore, we establish chromophoric DOM (CDOM) relationships to dissolved organic carbon (DOC) and lignin phenols in the Yukon River and model DOC and lignin loads from CDOM measurements, the former in excellent agreement with long-term DOC monitoring data. Intensive sampling across the historically under-sampled spring flush period highlights the importance of this time for total export of DOC and particularly lignin. Calculated riverine DOC loads to the Arctic Ocean show an increase from previous estimates, especially when new higher discharge data are incorporated. Increased DOC loads indicate decreased residence times for terrigenous DOM in the Arctic Ocean with important implications for the reactivity and export of this material to the Atlantic Ocean. Citation: Spencer, R. G. M., G. R. Aiken, K. D. Butler, M. M. Dornblaser, R. G. Striegl, and P. J. Hernes (2009), Utilizing chromophoric dissolved organic matter measurements to derive export and reactivity of dissolved organic carbon exported to the Arctic Ocean: A case study of the Yukon River, Alaska, Geophys. Res. Lett., 36, L06401, doi:10.1029/ 2008GL036831. Copyright 2009 by the American Geophysical Union.

SOMPROF: A vertically explicit soil organic matter model

NARCIS (Netherlands)

Braakhekke, M.C.; Beer, M.; Hoosbeek, M.R.; Kruijt, B.; Kabat, P.

2011-01-01

Most current soil organic matter (SOM) models represent the soil as a bulk without specification of the vertical distribution of SOM in the soil profile. However, the vertical SOM profile may be of great importance for soil carbon cycling, both on short (hours to years) time scale, due to

Effect of granular activated carbon concentration on the content of organic matter and salt, influencing E. coli activity and survival in fluidized bed disinfection reactor

NARCIS (Netherlands)

Racyte, J.; Langenhoff, A.A.M.; Ribeiro, A.F.M.M.R.; Paulitsch-Fuchs, A.H.; Bruning, H.; Rijnaarts, H.

2014-01-01

Granular activated carbon (GAC) is used in water treatment systems, typically to remove pollutants such as natural organic matter, volatile organic compounds, chlorine, taste, and odor. GAC is also used as a key component of a new technology that combines a fluidized bed reactor with radio frequency

Energy Transformations of Soil Organic Matter in a Changing World

Science.gov (United States)

Herrmann, A. M.; Coucheney, E.; Grice, S. M.; Ritz, K.; Harris, J.

2011-12-01

The role of soils in governing the terrestrial carbon balance is acknowledged as being important but remains poorly understood within the context of climate change. Soils exchange energy with their surroundings and are therefore open systems thermodynamically, but little is known how energy transformations of decomposition processes are affected by temperature. Soil organic matter and the soil biomass can be conceptualised as analogous to the 'fuel' and 'biological engine' of the earth, respectively, and are pivotal in driving the belowground carbon cycle. Thermodynamic principles of soil organic matter decomposition were evaluated by means of isothermal microcalorimetry (TAM Air, TA Instruments, Sollentuna Sweden: (i) Mineral forest soils from the Flakaliden long-term nitrogen fertilisation experiment (Sweden) were amended with a range of different substrates representing structurally simple to complex, ecologically pertinent organic matter and heat signatures were determined at temperatures between 5 and 25°C. (ii) Thermodynamic and resource-use efficiencies of the biomass were determined in arable soils which received contrasting long-term management regimes with respect to organic matter and nitrogen since 1956. The work showed that (i) structurally labile components have higher activation energy and temperature dependence than structurally more complex organic components. This is, however, in contrast to the thermodynamic argument which suggests the opposite that reactions metabolising structurally complex, aromatic components have higher temperature dependence than reactions metabolising structurally more labile components. (ii) Microbial communities exposed to long-term stress by heavy metal and low pH were less thermodynamic efficient and showed a decrease in resource-use efficiency in comparison with conventional input regimes. Differences in efficiencies were mirrored in both the phenotypic and functional profiles of the communities. We will present our

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

Extending the analytical window for water-soluble organic matter in sediments by aqueous Soxhlet extraction

Science.gov (United States)

Schmidt, Frauke; Koch, Boris P.; Witt, Matthias; Hinrichs, Kai-Uwe

2014-09-01

Dissolved organic matter (DOM) in marine sediments is a complex mixture of thousands of individual constituents that participate in biogeochemical reactions and serve as substrates for benthic microbes. Knowledge of the molecular composition of DOM is a prerequisite for a comprehensive understanding of the biogeochemical processes in sediments. In this study, interstitial water DOM was extracted with Rhizon samplers from a sediment core from the Black Sea and compared to the corresponding water-extractable organic matter fraction (Soxhlet extraction, which mobilizes labile particulate organic matter and DOM. After solid phase extraction (SPE) of DOM, samples were analyzed for the molecular composition by Fourier Transform Ion-Cyclotron Resonance Mass Spectrometry (FT-ICR MS) with electrospray ionization in negative ion mode. The average SPE extraction yield of the dissolved organic carbon (DOC) in interstitial water was 63%, whereas less than 30% of the DOC in Soxhlet-extracted organic matter was recovered. Nevertheless, Soxhlet extraction yielded up to 4.35% of the total sedimentary organic carbon, which is more than 30-times the organic carbon content of the interstitial water. While interstitial water DOM consisted primarily of carbon-, hydrogen- and oxygen-bearing compounds, Soxhlet extracts yielded more complex FT-ICR mass spectra with more peaks and higher abundances of nitrogen- and sulfur-bearing compounds. The molecular composition of both sample types was affected by the geochemical conditions in the sediment; elevated concentrations of HS- promoted the early diagenetic sulfurization of organic matter. The Soxhlet extracts from shallow sediment contained specific three- and four-nitrogen-bearing molecular formulas that were also detected in bacterial cell extracts and presumably represent proteinaceous molecules. These compounds decreased with increasing sediment depth while one- and two-nitrogen-bearing molecules increased, resulting in a higher

Organic matter and the geotechnical properties of submarine sediments

Science.gov (United States)

Keller, George H.

1982-09-01

Continental slope deposits off Peru and Oregon where coastal upwelling is a pronounced oceanographic process possess significant concentrations of organic carbon. Geotechnical properties are altered to varying degrees by the organic matter. Organic matter absorbs water and causes clay-size particles to aggregate forming an open fabric. This causes unusually high water contents and plasticity and exceptionally low wet bulk densities. Some of these deposits show notable increases in shear strength, sensitivity and degree of apparent overconsolidation. Owing to the unique geotechnical properties, sediment stability characteristics are considered to be poor in situations of excess pore pressures. Failure appears to take the form of a fluidized flow somewhat similar to the quick clays of Scandinavia.

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.

Urban infrastructure influences dissolved organic matter quality and bacterial metabolism in an urban stream network

Science.gov (United States)

Urban streams are degraded by a suite of factors, including burial beneath urban infrastructure (i.e., roads, parking lots) that eliminates light and reduces direct organic matter inputs to streams, with likely consequences for organic matter metabolism by microbes and carbon lim...

Stability of Soil Organic Matter in Alpine Ecosystems: No Relationship with Vegetation

Science.gov (United States)

Matteodo, M.; Sebag, D.; Vittoz, P.; Verrecchia, E. P.

2016-12-01

There is an emerging understanding of mechanisms governing soil organic matter (SOM) stability, which is challenging the historical view of carbon persistence1. According to this alternative vision, SOM stability is not directly regulated by the molecular structure of plant inputs (i.e. the historical view), but the biotic and abiotic conditions of the surrounding environment which play a major role and mediate the influence of compound chemistry. The persistence of SOM is thus influenced by ecological conditions, controlling the access and activity of decomposers' enzymes and being ecosystem-dependent. In this study, we investigated differences of (1) carbon content, and (2) stability of organic matter in litter and organomineral layers from the most widespread plant communities at the subalpine-alpine level of the Swiss Alps. For this purpose, 230 samples from 47 soil profiles have been analysed across seven plant communities, along a subalpine-alpine elevation gradient. Both calcareous and siliceous grasslands were studied, as well as snowbed and ridge communities. Aboveground litter and A horizons were sampled and analysed using Rock-Eval Pyrolysis, a proxy-technique commonly used for the investigation of organic matter composition and stability2,3. Results show that the litter layers of the seven plant communities are significantly different in terms of total organic carbon (TOC) content, but slightly variable in terms of stability. The situation is radically different in the organomineral horizons where the amount of organic carbon is interestingly homogeneous, as well as the SOM stability. In mineral horizons, the amount and stability of SOM are mainly driven by the geological settings, and therefore vary in the different plant communities. These results show a clear disconnection between organic, organomineral, and mineral horizons in terms of factors governing soil organic matter stability. Consistent with the recent view of the carbon balance, plant input

THE USE OF BIOFILTRATION PROCESS TO REMOVE ORGANIC MATTER FROM GROUNDWATER

Directory of Open Access Journals (Sweden)

Dorota Papciak

2016-07-01

Full Text Available The article describes the research on the removal of organic matter from natural underground water using biofiltration process. The study was carried out in semi-technical scale on a model filter composed of activated carbon WD-extra. The development of biological activity in a biosorption bed, as well as observations on the relationship between the processes of sorption and biodegradation was evaluated based on the Eberhardt, Madsen, Sontheimer (EMS test. Leading operation control parameters of biologically active carbon filter BAF included: change of TOC content, dissolved oxygen and permanganate index. To evaluate the colonization of granular carbon determination of ATP value was used. The presence of the biofilm was found by observation using light and scanning microscopes. The organic compounds in the water taken were adsorbed 100% and 70% biodegradable. The combination of sorption process with biodegradation until depletion of activated carbon adsorption capacity allowed in the initial phase of coalbed work for the removal of organic matter in approx. 100% . Formation of biofilm at the right time allowed to extend the filtration cycle and helped lower the TOC by 70%, i.e. from 10 mg C/l to 3-4 mg C/l.

Organic matter and soil moisture content and double cropping with organic matter sourceplants

OpenAIRE

John Bako Baon; Aris Wibawa

2005-01-01

Double cropping of coffee with organic matter source plants is thought to increase organic matter content of soil. This study examined the effect of double cropping of coffee and organic matter source plants on soil organic matter content and yield of coffee plants. Arabica coffee trees in Andungsari Experimental Station (Bondowoso district), 1400 m asl. and climate type C; and Robusta coffee trees in Sumberasin Experimental Station (Malang district), 550 m asl. and climate type C, were used ...

Linking geochemical processes in mud volcanoes with arsenic mobilization driven by organic matter

Energy Technology Data Exchange (ETDEWEB)

Liu, Chia-Chuan; Kar, Sandeep [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Jean, Jiin-Shuh, E-mail: jiinshuh@mail.ncku.edu.tw [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Wang, Chung-Ho [Institute of Earth Sciences, Academia Sinica, Taipei, Taiwan (China); Lee, Yao-Chang [National Synchrotron Radiation Research Center, Hsinchu 30076, Taiwan (China); Sracek, Ondra [OPV s.r.o. (Groundwater Protection Ltd.), Bělohorská 31, 169 00 Praha 6 (Czech Republic); Department of Geology, Faculty of Science, Palacký University, 17. listopadu 12, 771 46 Olomouc (Czech Republic); Li, Zhaohui [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Department of Geosciences, University of Wisconsin – Parkside, Kenosha, WI 53144 (United States); Bundschuh, Jochen [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Faculty of Engineering and Surveying and National Centre for Engineering in Agriculture, The University of Southern Queensland, Toowoomba (Australia); Yang, Huai-Jen [Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan (China); Chen, Chien-Yen [Department of Earth and Environmental Sciences, National Chung Cheng University, Chiayi 621, Taiwan (China)

2013-11-15

Highlights: ► Study represents geochemical characteristics and their spatial variability among six mud volcanoes of southern Taiwan. ► Anoxic mud volcanic fluids containing high NaCl imply connate water as the possible source. ► δ{sup 18}O-rich fluids is associated with silicate and carbonate mineral released through water–rock interaction. ► High As content in mud and its sequential extraction showed mostly adsorbed As on organic and sulphidic phases. ► Organic matter specially humic acid showed redox dependence and it may play an important role in binding and mobility of arsenic. -- Abstract: The present study deals with geochemical characterization of mud fluids and sediments collected from Kunshuiping (KSP), Liyushan (LYS), Wushanting (WST), Sinyangnyuhu (SYNH), Hsiaokunshui (HKS) and Yenshuikeng (YSK) mud volcanoes in southwestern Taiwan. Chemical constituents (cations, anions, trace elements, organic carbon, humic acid, and stable isotopes) in both fluids and mud were analyzed to investigate the geochemical processes and spatial variability among the mud volcanoes under consideration. Analytical results suggested that the anoxic mud volcanic fluids are highly saline, implying connate water as the probable source. The isotopic signature indicated that δ{sup 18}O-rich fluids may be associated with silicate and carbonate mineral released through water–rock interaction, along with dehydration of clay minerals. Considerable amounts of arsenic in mud irrespective of fluid composition suggested possible release through biogeochemical processes in the subsurface environment. Sequential extraction of As from the mud indicated that As was mostly present in organic and sulphidic phases, and adsorbed on amorphous Mn oxyhydroxides. Volcanic mud and fluids are rich in organic matter (in terms of organic carbon), and the presence of humic acid in mud has implications for the binding of arsenic. Functional groups of humic acid also showed variable sources of

Predicting nitrogen and acidity effects on long-term dynamics of dissolved organic matter

International Nuclear Information System (INIS)

Rowe, E.C.; Tipping, E.; Posch, M.; Oulehle, F.; Cooper, D.M.; Jones, T.G.; Burden, A.; Hall, J.; Evans, C.D.

2014-01-01

Increases in dissolved organic carbon (DOC) fluxes may relate to changes in sulphur and nitrogen pollution. We integrated existing models of vegetation growth and soil organic matter turnover, acid–base dynamics, and organic matter mobility, to form the ‘MADOC’ model. After calibrating parameters governing interactions between pH and DOC dissolution using control treatments on two field experiments, MADOC reproduced responses of pH and DOC to additions of acidifying and alkalising solutions. Long-term trends in a range of acid waters were also reproduced. The model suggests that the sustained nature of observed DOC increases can best be explained by a continuously replenishing potentially-dissolved carbon pool, rather than dissolution of a large accumulated store. The simulations informed the development of hypotheses that: DOC increase is related to plant productivity increase as well as to pH change; DOC increases due to nitrogen pollution will become evident, and be sustained, after soil pH has stabilised. -- Highlights: • A model of dissolved organic carbon (DOC) was developed by integrating simple models • MADOC simulates effects of sulphur and nitrogen deposition and interactions with pH. • Responses of DOC and pH to experimental acidification and alkalisation were reproduced. • The persistence of DOC increases will depend on continued supply of potential DOC. • DOC fluxes are likely determined by plant productivity as well as soil solution pH. -- Effects of changes in sulphur and nitrogen pollution on dissolved organic carbon fluxes are predicted by simulating soil organic matter cycling, the release of potentially-dissolved carbon, and interactions with soil pH

Formation and Stability of Microbially Derived Soil Organic Matter

Science.gov (United States)

Waldrop, M. P.; Creamer, C.; Foster, A. L.; Lawrence, C. R.; Mcfarland, J. W.; Schulz, M. S.

2017-12-01

Soil carbon is vital to soil health, food security, and climate change mitigation, but the underlying mechanisms controlling the stabilization and destabilization of soil carbon are still poorly understood. There has been a conceptual paradigm shift in how soil organic matter is formed which now emphasizes the importance of microbial activity to build stable (i.e. long-lived) and mineral-associated soil organic matter. In this conceptual model, the consumption of plant carbon by microorganisms, followed by subsequent turnover of microbial bodies closely associated with mineral particles, produces a layering of amino acid and lipid residues on the surfaces of soil minerals that remains protected from destabilization by mineral-association and aggregation processes. We tested this new model by examining how isotopically labeled plant and microbial C differ in their fundamental stabilization and destabilization processes on soil minerals through a soil profile. We used a combination of laboratory and field-based approaches to bridge multiple spatial scales, and used soil depth as well as synthetic minerals to create gradients of soil mineralogy. We used Raman microscopy as a tool to probe organic matter association with mineral surfaces, as it allows for the simultaneous quantification and identification of living microbes, carbon, minerals, and isotopes through time. As expected, we found that the type of minerals present had a strong influence on the amount of C retained, but the stabilization of new C critically depends on growth, death, and turnover of microbial cells. Additionally, the destabilization of microbial residue C on mineral surfaces was little affected by flushes of DOC relative to wet-dry cycles alone. We believe this new insight into microbial mechanisms of C stabilization in soils will eventually lead to new avenues for measuring and modeling SOM dynamics in soils, and aid in the management of soil C to mediate global challenges.

Riverine transport of terrestrial organic matter to the North Catalan margin, NW Mediterranean Sea

Science.gov (United States)

Sanchez-Vidal, Anna; Higueras, Marina; Martí, Eugènia; Liquete, Camino; Calafat, Antoni; Kerhervé, Philippe; Canals, Miquel

2013-11-01

Rivers are the primary pathway for organic matter transport from the terrestrial to the marine environment and, thus, river fluxes are critical in regulating the quantity of terrestrial organic matter that reaches the coastal ecosystems. Hydrodynamic processes typical of the coastal zone can lead to the transport of terrestrial organic matter across the continental shelf and beyond. Such organic matter can eventually reach the deep margin and basin ecosystems. Riverine inputs of organic matter to the sea can be a significant food source to marine ecosystems contributing to carbon cycling in these ecosystems. In order to assess the marine carbon cycle it is essential to know the biogeochemical characteristics and temporal dynamics of the fluvial organic matter input discharged by rivers to the coastal zone. In this study we present a one and a half year long (November 2008 to May 2010) assessment on organic carbon (OC) and nitrogen (N) inputs from the three main rivers discharging into the North Catalan margin (Tordera, Ter and Fluvià, from south to north). Furthermore, we investigate the characteristics of the particulate organic matter discharged by these rivers by means of stable isotopic (δ13C and δ15N) and grain size analyses. We found that the hydrological regime of the rivers is a relevant factor in regulating the quantity and mediating the quality of organic matter inputs to the North Catalan margin. Overall, the three main rivers discharging into the study area deliver 1266 and 159 tonnes of terrestrial OC and N per year, respectively, to the coastal zone. Most of the OC and N load is transported during floods, which indicates that the Mediterranean climate of the area, with a strong seasonal contrast in precipitation, determines the timing of the main inputs of OC and N to the sea. Therefore, the annual OC and N load experiences a high temporal variability associated to the number and magnitude of floods with in each hydrological year. In addition, we

Utilizing Colored Dissolved Organic Matter to Derive Dissolved Black Carbon Export by Arctic Rivers

Science.gov (United States)

Stubbins, Aron; Spencer, Robert; Mann, Paul; Holmes, R.; McClelland, James; Niggemann, Jutta; Dittmar, Thorsten

2015-10-01

Wildfires have produced black carbon (BC) since land plants emerged. Condensed aromatic compounds, a form of BC, have accumulated to become a major component of the soil carbon pool. Condensed aromatics leach from soils into rivers, where they are termed dissolved black carbon (DBC). The transport of DBC by rivers to the sea is a major term in the global carbon and BC cycles. To estimate Arctic river DBC export, 25 samples collected from the six largest Arctic rivers (Kolyma, Lena, Mackenzie, Ob’, Yenisey and Yukon) were analyzed for dissolved organic carbon (DOC), colored dissolved organic matter (CDOM), and DBC. A simple, linear regression between DOC and DBC indicated that DBC accounted for 8.9 ± 0.3% DOC exported by Arctic rivers. To improve upon this estimate, an optical proxy for DBC was developed based upon the linear correlation between DBC concentrations and CDOM light absorption coefficients at 254 nm (a254). Relatively easy to measure a254 values were determined for 410 Arctic river samples between 2004 and 2010. Each of these a254 values was converted to a DBC concentration based upon the linear correlation, providing an extended record of DBC concentration. The extended DBC record was coupled with daily discharge data from the six rivers to estimate riverine DBC loads using the LOADEST modeling program. The six rivers studied cover 53% of the pan-Arctic watershed and exported 1.5 ± 0.1 million tons of DBC per year. Scaling up to the full area of the pan-Arctic watershed, we estimate that Arctic rivers carry 2.8 ± 0.3 million tons of DBC from land to the Arctic Ocean each year. This equates to ~8% of Arctic river DOC export, slightly less than indicated by the simpler DBC vs DOC correlation-based estimate. Riverine discharge is predicted to increase in a warmer Arctic. DBC export was positively correlated with river runoff, suggesting that the export of soil BC to the Arctic Ocean is likely to increase as the Arctic warms.

Utilizing Colored Dissolved Organic Matter to Derive Dissolved Black Carbon Export by Arctic Rivers

Directory of Open Access Journals (Sweden)

Aron eStubbins

2015-10-01

Full Text Available Wildfires have produced black carbon (BC since land plants emerged. Condensed aromatic compounds, a form of BC, have accumulated to become a major component of the soil carbon pool. Condensed aromatics leach from soils into rivers, where they are termed dissolved black carbon (DBC. The transport of DBC by rivers to the sea is a major term in the global carbon and BC cycles. To estimate Arctic river DBC export, 25 samples collected from the six largest Arctic rivers (Kolyma, Lena, Mackenzie, Ob’, Yenisey and Yukon were analyzed for dissolved organic carbon (DOC, colored dissolved organic matter (CDOM, and DBC. A simple, linear regression between DOC and DBC indicated that DBC accounted for 8.9 ± 0.3% DOC exported by Arctic rivers. To improve upon this estimate, an optical proxy for DBC was developed based upon the linear correlation between DBC concentrations and CDOM light absorption coefficients at 254 nm (a254. Relatively easy to measure a254 values were determined for 410 Arctic river samples between 2004 and 2010. Each of these a254 values was converted to a DBC concentration based upon the linear correlation, providing an extended record of DBC concentration. The extended DBC record was coupled with daily discharge data from the six rivers to estimate riverine DBC loads using the LOADEST modeling program. The six rivers studied cover 53% of the pan-Arctic watershed and exported 1.5 ± 0.1 million tons of DBC per year. Scaling up to the full area of the pan-Arctic watershed, we estimate that Arctic rivers carry 2.8 ± 0.3 million tons of DBC from land to the Arctic Ocean each year. This equates to ~8% of Arctic river DOC export, slightly less than indicated by the simpler DBC vs DOC correlation-based estimate. Riverine discharge is predicted to increase in a warmer Arctic. DBC export was positively correlated with river runoff, suggesting that the export of soil BC to the Arctic Ocean is likely to increase as the Arctic warms.

Heterogeneous carbonaceous matter in sedimentary rock lithocomponents causes significant trichloroethylene (TCE) sorption in a low organic carbon content aquifer/aquitard system.

Science.gov (United States)

Choung, Sungwook; Zimmerman, Lisa R; Allen-King, Richelle M; Ligouis, Bertrand; Feenstra, Stanley

2014-10-15

This study evaluated the effects of heterogeneous thermally altered carbonaceous matter (CM) on trichloroethylene (TCE) sorption for a low fraction organic carbon content (foc) alluvial sedimentary aquifer and aquitard system (foc=0.046-0.105%). The equilibrium TCE sorption isotherms were highly nonlinear with Freundlich exponents of 0.46-0.58. Kerogen+black carbon was the dominant CM fraction extracted from the sediments and accounted for >60% and 99% of the total in the sands and silt, respectively. Organic petrological examination determined that the kerogen included abundant amorphous organic matter (bituminite), likely of marine origin. The dark calcareous siltstone exhibited the greatest TCE sorption among aquifer lithocomponents and accounted for most sorption in the aquifer. The results suggest that the source of the thermally altered CM, which causes nonlinear sorption, was derived from parent Paleozoic marine carbonate rocks that outcrop throughout much of New York State. A synthetic aquifer-aquitard unit system (10% aquitard) was used to illustrate the effect of the observed nonlinear sorption on mass storage potential at equilibrium. The calculation showed that >80% of TCE mass contained in the aquifer was sorbed on the aquifer sediment at aqueous concentration TCE groundwater plume in the aquifer studied. It is implied that sorption may similarly contribute to TCE persistence in other glacial alluvial aquifers with similar geologic characteristics, i.e., comprised of sedimentary rock lithocomponents that contain thermally altered CM. Copyright © 2014 Elsevier B.V. All rights reserved.

Assessing the stability of soil organic matter by fractionation and 13C isotope techniques

Science.gov (United States)

Larionova, A. A.; Zolotareva, B. N.; Kvitkina, A. K.; Evdokimov, I. V.; Bykhovets, S. S.; Stulin, A. F.; Kuzyakov, Ya. V.; Kudeyarov, V. N.

2015-02-01

Carbon pools of different stabilities have been separated from the soil organic matter of agrochernozem and agrogray soil samples. The work has been based on the studies of the natural abundance of the carbon isotope composition by C3-C4 transition using the biokinetic, size-density, and chemical fractionation (6 M HCl hydrolysis) methods. The most stable pools with the minimum content of new carbon have been identified by particle-size and chemical fractionation. The content of carbon in the fine fractions has been found to be close to that in the nonhydrolyzable residue. This pool makes up 65 and 48% of Corg in the agrochernozems and agrogray soils, respectively. The combination of the biokinetic approach with particle-size fractionation or 6 M HCl hydrolysis has allowed assessing the size of the medium-stable organic carbon pool with a turnover time of several years to several decades. The organic matter pool with this turnover rate is usually identified from the variation in the 13C abundance by C3-C4 transition. In the agrochernozems and agrogray soils, the medium-stable carbon pool makes up 35 and 46% of Corg, respectively. The isotope indication may be replaced by a nonisotope method to significantly expand the study of the inert and mediumstable organic matter pools in the geographical aspect, but this requires a comparative analysis of particle-size and chemical fractionation data for all Russian soils.

River inputs and organic matter fluxes in the northern Bay of Bengal: Fatty acids

Digital Repository Service at National Institute of Oceanography (India)

Reemtsma, T.; Ittekkot, V.; Bartsch, M.; Nair, R.R

) 55-71 55 Elsevier Science Publishers B.V., Amsterdam \\[RA\\] River inputs and organic matter fluxes in the northern Bay of Bengal: fatty acids T. Reemtsma a, V. Ittekkot a, M. Bartsch a and R.R. Nair b alnstitut fiir Biogeochemie und Meereschemie..., R.R., 1993. River inputs and organic matter fluxes in the northern Bay of Bengal: fatty acids. Chem. Geol., 103: 55-71. Total particulate matter flux and organic carbon and fatty acid fluxes associated with settling particles collected during...

Influence of sulfate reduction on the organic matter of Wealden sediments of the Lower Saxony Basin (Germany)

Energy Technology Data Exchange (ETDEWEB)

Berner, U. [Bundesanstalt fuer Geowissenschaften und Rohstoffe (BGR), Hannover (Germany)

2013-08-01

Sediments of the Wealden (Lower Saxony Basin, Germany) as obtained from the well Isterberg 1001 consist of clay stones, marls and few massive carbonate horizons. Although, the basin is predominantly characterized as lacustrine geochemical data indicate significant influences of marine ingression which have introduced sulfur into the depositional system. Consequently the organic matter of the sediments has been substantially affected by bacterial sulfate reduction, which has led to losses of the initial organic carbon of 5 to 80 wt.- percent, which is a minimum estimate as losses of H{sub 2}S form the sediments were not taken into account for the mass balance consideration. Complete uptake of reactive iron into sulfides has led in a significant number of samples to the presence of excess sulfur not contained in sulfides. In our argumentation we assume that excess sulfur is at least partly incorporated into the organic matter. Pyrolysis investigations show that organic matter in samples containing higher amounts of excess sulfur generates hydrocarbons at lower temperatures than samples with low concentrations of excess sulfur. These observations are compatible with findings usually reported for Type S-II kerogens. The likely organically bound excess sulfur introduces a bias with thermal maturities from RockEval pyrolysis, which implies that T{sub max} data rather reflect quality changes of the organic matter than thermal maturity in the investigated Wealden sediments. The hydrocarbon potential has been reduced significantly in samples which have been affected strongly by the microbial process as indicated by hydrogen indices of the sediments. The observations of variable degrees of sulfate reduction indicate also a variation of organic matter fluxes to the sediment surface of the palaeo-lake likely resulting from changes in biological surface productivity. Low carbon fluxes likely coincide with extensive use of organic substrate by sulfate reducers whereas high

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

Processes and modeling of hydrolysis of particulate organic matter in aerobic wastewater tratment - A review

DEFF Research Database (Denmark)

Morgenroth, Eberhard Friedrich; Kommedal, Roald; Harremoës, Poul

2002-01-01

Carbon cycling and the availability of organic carbon for nutrient removal processes are in most wastewater treatment systems restricted by the rate of hydrolysis of slowly biodegradable (particulate) organic matter. To date, the mechanisms of hydrolysis are not well understood for complex...

Predicting nitrogen and acidity effects on long-term dynamics of dissolved organic matter

OpenAIRE

Rowe, E.C.; Tipping, E.; Posch, M.; Oulehle, Filip; Cooper, D.M.; Jones, T.G.; Burden, A.; Hall, J.; Evans, C.D.

2014-01-01

Increases in dissolved organic carbon (DOC) fluxes may relate to changes in sulphur and nitrogen pollution. We integrated existing models of vegetation growth and soil organic matter turnover, acid-base dynamics, and organic matter mobility, to form the ‘MADOC’ model. After calibrating parameters governing interactions between pH and DOC dissolution using control treatments on two field experiments, MADOC reproduced responses of pH and DOC to additions of acidifying and alkalising solutions. ...

Organic carbon production, mineralization and preservation on the Peruvian margin

Science.gov (United States)

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

2014-09-01

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

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

Effects of natural organic matter on PCB-activated carbon sorption kinetics: implications for sediment capping applications.

Science.gov (United States)

Fairey, Julian L; Wahman, David G; Lowry, Gregory V

2010-01-01

In situ capping of polychlorinated biphenyl (PCB)-contaminated sediments with a layer of activated carbon has been proposed, but several questions remain regarding the long-term effectiveness of this remediation strategy. Here, we assess the degree to which kinetic limitations, size exclusion effects, and electrostatic repulsions impaired PCB sorption to activated carbon. Sorption of 11 PCB congeners with activated carbon was studied in fixed bed reactors with organic-free water (OFW) and Suwannee River natural organic matter (SR-NOM), made by reconstituting freeze-dried SR-NOM at a concentration of 10 mg L(-1) as carbon. In the OFW test, no PCBs were detected in the column effluent over the 390-d study, indicating that PCB-activated carbon equilibrium sorption capacities may be achieved before breakthrough even at the relatively high hydraulic loading rate (HLR) of 3.1 m h(-1). However, in the SR-NOM fixed-bed test, partial PCB breakthrough occurred over the entire 320-d test (HLRs of 3.1-, 1.5-, and 0.8 m h(-1)). Simulations from a modified pore and surface diffusion model indicated that external (film diffusion) mass transfer was the dominant rate-limiting step but that internal (pore diffusion) mass transfer limitations were also present. The external mass transfer limitation was likely caused by formation of PCB-NOM complexes that reduced PCB sorption through a combination of (i) increased film diffusion resistance; (ii) size exclusion effects; and (iii) electrostatic repulsive forces between the PCBs and the NOM-coated activated carbon. However, the seepage velocities in the SR-NOM fixed bed test were about 1000 times higher than would be expected in a sediment cap. Therefore, additional studies are needed to assess whether the mass transfer limitations described here would be likely to manifest themselves at the lower seepage velocities observed in practice.

Effects of added organic matter and water on soil carbon sequestration in an arid region.

Directory of Open Access Journals (Sweden)

Liming Lai

Full Text Available It is generally predicted that global warming will stimulate primary production and lead to more carbon (C inputs to soil. However, many studies have found that soil C does not necessarily increase with increased plant litter input. Precipitation has increased in arid central Asia, and is predicted to increase more, so we tested the effects of adding fresh organic matter (FOM and water on soil C sequestration in an arid region in northwest China. The results suggested that added FOM quickly decomposed and had minor effects on the soil organic carbon (SOC pool to a depth of 30 cm. Both FOM and water addition had significant effects on the soil microbial biomass. The soil microbial biomass increased with added FOM, reached a maximum, and then declined as the FOM decomposed. The FOM had a more significant stimulating effect on microbial biomass with water addition. Under the soil moisture ranges used in this experiment (21.0%-29.7%, FOM input was more important than water addition in the soil C mineralization process. We concluded that short-term FOM input into the belowground soil and water addition do not affect the SOC pool in shrubland in an arid region.

Mechanistic modelling of the vertical soil organic matter profile

NARCIS (Netherlands)

Braakhekke, M.C.

2014-01-01

Soil organic matter (SOM) constitutes a large global pool of carbon that may play a considerable role for future climate. The vertical distribution of SOM in the profile may be important due to depth-dependence of physical, chemical, and biological conditions, and links to physical processes

Linking geochemical processes in mud volcanoes with arsenic mobilization driven by organic matter.

Science.gov (United States)

Liu, Chia-Chuan; Kar, Sandeep; Jean, Jiin-Shuh; Wang, Chung-Ho; Lee, Yao-Chang; Sracek, Ondra; Li, Zhaohui; Bundschuh, Jochen; Yang, Huai-Jen; Chen, Chien-Yen

2013-11-15

The present study deals with geochemical characterization of mud fluids and sediments collected from Kunshuiping (KSP), Liyushan (LYS), Wushanting (WST), Sinyangnyuhu (SYNH), Hsiaokunshui (HKS) and Yenshuikeng (YSK) mud volcanoes in southwestern Taiwan. Chemical constituents (cations, anions, trace elements, organic carbon, humic acid, and stable isotopes) in both fluids and mud were analyzed to investigate the geochemical processes and spatial variability among the mud volcanoes under consideration. Analytical results suggested that the anoxic mud volcanic fluids are highly saline, implying connate water as the probable source. The isotopic signature indicated that δ(18)O-rich fluids may be associated with silicate and carbonate mineral released through water-rock interaction, along with dehydration of clay minerals. Considerable amounts of arsenic in mud irrespective of fluid composition suggested possible release through biogeochemical processes in the subsurface environment. Sequential extraction of As from the mud indicated that As was mostly present in organic and sulphidic phases, and adsorbed on amorphous Mn oxyhydroxides. Volcanic mud and fluids are rich in organic matter (in terms of organic carbon), and the presence of humic acid in mud has implications for the binding of arsenic. Functional groups of humic acid also showed variable sources of organic matter among the mud volcanoes being examined. Because arsenate concentration in the mud fluids was found to be independent from geochemical factors, it was considered that organic matter may induce arsenic mobilization through an adsorption/desorption mechanism with humic substances under reducing conditions. Organic matter therefore plays a significant role in the mobility of arsenic in mud volcanoes. Copyright © 2012 Elsevier B.V. All rights reserved.

Experimental Study of Soil Organic Matter Loss From Cultivated Field Plots In The Venezuelan Andes.

Science.gov (United States)

Bellanger, B.; Huon, S.; Velasquez, F.; Vallès, V.; Girardin A, C.; Mariotti, A. B.

The question of discriminating sources of organic matter in suspended particles of stream flows can be addressed by using total organic carbon (TOC) concentration and stable isotope (13C, 15N) measurements when constant fluxes of organic matter supply can be assumed. However, little is known on the dynamics of organic matter release during soil erosion and on the temporal stability of its isotopic signature. In this study, we have monitored soil organic carbon loss and water runoff using natural rainfall events on three experimental field plots with different vegetation cover (bare soil, maize and coffee fields), set up on natural slopes of a tropical mountainous watershed in NW Venezuela (09°13'32'' ­ 09°10'00''N, 70°13'49'' ­ 70°18'34''W). Runoff and soil loss are markedly superior for the bare field plot than for the coffee field plot: by a factor 15 ­ 36, respectively, for the five-month experiment, and by a factor 30 ­ 120, respectively, during a single rainfall event experiment. Since runoff and soil organic matter loss are closely linked during most of the flow (at the time scales of this study), TOC concentration in suspended matter is constant. Furthermore, stable isotope compositions reflect those of top-soil organic matter from which they originate.

Effect of biochar amendment on compost organic matter composition following aerobic composting of manure.

Science.gov (United States)

Hagemann, Nikolas; Subdiaga, Edisson; Orsetti, Silvia; de la Rosa, José María; Knicker, Heike; Schmidt, Hans-Peter; Kappler, Andreas; Behrens, Sebastian

2018-02-01

Biochar, a material defined as charred organic matter applied in agriculture, is suggested as a beneficial additive and bulking agent in composting. Biochar addition to the composting feedstock was shown to reduce greenhouse gas emissions and nutrient leaching during the composting process, and to result in a fertilizer and plant growth medium that is superior to non-amended composts. However, the impact of biochar on the quality and carbon speciation of the organic matter in bulk compost has so far not been the focus of systematic analyses, although these parameters are key to determine the long-term stability and carbon sequestration potential of biochar-amended composts in soil. In this study, we used different spectroscopic techniques to compare the organic carbon speciation of manure compost amended with three different biochars. A non-biochar-amended compost served as control. Based on Fourier-transformed infrared (FTIR) and 13 C nuclear magnetic resonance (NMR) spectroscopy we did not observe any differences in carbon speciation of the bulk compost independent of biochar type, despite a change in the FTIR absorbance ratio 2925cm -1 /1034cm -1 , that is suggested as an indicator for compost maturity. Specific UV absorbance (SUVA) and emission-excitation matrixes (EEM) revealed minor differences in the extractable carbon fractions, which only accounted for ~2-3% of total organic carbon. Increased total organic carbon content of biochar-amended composts was only due to the addition of biochar-C and not enhanced preservation of compost feedstock-C. Our results suggest that biochars do not alter the carbon speciation in compost organic matter under conditions optimized for aerobic decomposition of compost feedstock. Considering the effects of biochar on compost nutrient retention, mitigation of greenhouse gas emissions and carbon sequestration, biochar addition during aerobic composting of manure might be an attractive strategy to produce a sustainable, slow

Investigation of the organic matter in inactive nuclear tank liquids

International Nuclear Information System (INIS)

Schenley, R.L.; Griest, W.H.

1990-08-01

Environmental Protection Agency (EPA) methodology for regulatory organics fails to account for the organic matter that is suggested by total organic carbon (TOC) analysis in the Oak Ridge National Laboratory (ORNL) inactive nuclear waste-tank liquids and sludges. Identification and measurement of the total organics are needed to select appropriate waste treatment technologies. An initial investigation was made of the nature of the organics in several waste-tank liquids. This report details the analysis of ORNL wastes

Dynamics of Dissolved Organic Matter and Microbes in Seawater through Sub-Micron Particle Size Analyses

Digital Repository Service at National Institute of Oceanography (India)

Goes, J.I.; Balch, W.M.; Vaughn, J.M.; Gomes, H.R.

-78. Hansell, D.A. and Carlson, C.A., (1998) Deep-ocean gradients in the concentration of dissolved organic carbon. Nature, 395, 263-266. J. E. (1977) Characterization of suspended matter in the Gulf of Mexico ? II. Particles size analysis of suspended matter.... and Morris, I. (1980) Extracellular release of carbon by marine phytoplankton: a physiological approach. Limnol. Oceanogr., 25, 262-279. Maurer, L. G. (1976) Organic polymers in seawater: changes with depth in the Gulf of Mexico. Deep-Sea Res., 23, 1059...

Origin and availability of organic matter leading to arsenic mobilisation in aquifers of the Red River Delta, Vietnam

International Nuclear Information System (INIS)

Eiche, Elisabeth; Berg, Michael; Hönig, Sarah-Madeleine; Neumann, Thomas; Lan, Vi Mai; Pham, Thi Kim Trang; Pham, Hung Viet

2017-01-01

Groundwater arsenic (As) concentrations in the Red River Delta (Vietnam) are often patchy and related to the microbially induced reduction of Fe oxy-hydroxides. In this study, we explored the influence of the origin, composition and availability of natural organic matter on the hydrochemical variability in the aquifers of Van Phuc. Carbon isotope signatures (δ"1"3C_o_r_g) and C/N ratios were assessed in combination with lithology, geochemistry, hydrochemistry, hydrology and the distribution of specific biomarkers. The elationship of C/N ratios and δ"1"3C_o_r_g distinguished four groups of sediment types that differ in their organic carbon sources. This includes organic carbon originating predominantly from vascular C_3 plants (C/N: 15.4–21.0, δ"1"3C_o_r_g: −28.6 to −26.7‰), C_4 plants (C/N: 10.6; δ"1"3C_o_r_g: −14.8‰), freshwater derived particulate organic carbon (C/N: ≤8; δ"1"3C_o_r_g:≤−24‰) as well as mixtures incorporating both sources. At the high As sites, we found particulate organic carbon (POC) being 1–2‰ less depleted in δ"1"3C_o_r_g than at low As sites. More importantly, however, our assessment shows that, the availability of organic matter has to be considered decisive with regard to groundwater As contamination. Fine-grained clayey sediments overlaying sands generally protect organic matter from substantial degradation and its leaching into an adjacent aquifer. However, at the sites that are high in dissolved As in Van Phuc, sediment layers rich in organic matter are hydraulically connected to the underlying aquifer. Here, soluble organic matter seeping into the aquifer can induce and/or enhance reducing conditions, thereby mobilising As from Fe oxy-hydroxides. Our study shows that both the clay content as well as the origin of organic matter are largely controlled by the depositional environment of the sediments. - Highlights: • Particulate organic carbon (POC) from C_3/C_4 plants and freshwater is a main source of

Microbial Contribution to Organic Carbon Sequestration in Mineral Soil

Science.gov (United States)

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

Significance of Isotopically Labile Organic Hydrogen in Thermal Maturation of Organic Matter

Energy Technology Data Exchange (ETDEWEB)

Arndt Schimmelmann; Maria Mastalerz

2010-03-30

Isotopically labile organic hydrogen in fossil fuels occupies chemical positions that participate in isotopic exchange and in chemical reactions during thermal maturation from kerogen to bitumen, oil and gas. Carbon-bound organic hydrogen is isotopically far less exchangeable than hydrogen bound to nitrogen, oxygen, or sulfur. We explore why organic hydrogen isotope ratios express a relationship with organic nitrogen isotope ratios in kerogen at low to moderate maturity. We develop and apply new techniques to utilize organic D/H ratios in organic matter fractions and on a molecular level as tools for exploration for fossil fuels and for paleoenvironmental research. The scope of our samples includes naturally and artificially matured substrates, such as coal, shale, oil and gas.

Intra-annual variability of carbon and nitrogen stable isotopes in suspended organic matter in waters of the western continental shelf of India

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M. V. Maya

2011-11-01

Full Text Available Intra-annual variations of δ¹³C and δ¹⁵N of water-column suspended particulate organic matter (SPOM have been investigated to understand the biogeochemical cycling of C and N in the Western Continental Shelf of India (WCSI. The key issues being addressed are: how the δ¹⁵N of SPOM is affected by seasonally varying processes of organic matter production and respiration and how it relates to the δ¹⁵N of sedimentary organic matter that appears to show a decreasing trend despite an apparent intensification of seasonal oxygen deficiency over the past few decades? A secondary objective was to evaluate the sources of organic carbon. Elemental carbon and nitrogen concentrations, C/N ratios in SPOM, along with ancillary chemical and biological variables including phytoplankton pigment abundance were also determined on a seasonal basis (from March 2007 to September 2008, with the partial exception of the southwest (SW monsoon period. The results reveal significant shifts in isotopic signatures, especially δ¹⁵N, of SPOM before and after the onset of SW monsoon. Very low δ¹⁵N values, reaching a minimum of −4.17 ‰, are found during the pre-monsoon period. Our results provide the first direct evidence for the addition of substantial amounts of isotopically light nitrogen by the diazotrophs, especially Trichodesmium, in the region. The δ¹⁵N of SPOM is generally lower than the mean value (7.38 ‰ for surficial sediments, presumably because of diagenetic enrichment. The results support the view that sedimentary δ¹⁵N may not necessarily reflect denitrification intensity in the overlying waters due to diverse sources of nitrogen and variability of its isotopic composition. The observed intra-annual variability of δ¹³C of SPOM during the pre-monsoon and post-monsoon periods is generally small. Phytoplankton production and probably species

Evaluating the effectiveness of mulch application to store carbon belowground: Short-term effects of mulch application on soluble soil and microbial C and N in agricultural soils with low and high organic matter

Science.gov (United States)

Chen, Janet; Heiling, Maria; Resch, Christian; Gruber, Roman; Dercon, Gerd

2017-04-01

Agricultural soils have the potential to contain a large pool of carbon and, depending on the farming techniques applied, can either effectively store carbon belowground, or further release carbon, in the form of CO2, into the atmosphere. Farming techniques, such as mulch application, are frequently proposed to increase carbon content belowground and improve soil quality and can be used in efforts to reduce greenhouse gas levels, such as in the "4 per 1000" Initiative. To test the effectiveness of mulch application to store carbon belowground in the short term and improve soil nutrient quality, we maintained agricultural soils with low and high organic carbon content (disturbed top soil from local Cambisols and Chernozems) in greenhouse mesocosms (70 cm deep with a radius of 25 cm) with controlled moisture for 4 years. Over the 4 years, maize and soybean were grown yearly in rotation and mulch was removed or applied to soils once plant material was harvested at 2 ton/ha dry matter. In addition, soil disturbance was kept to a minimum, with only surface disturbance of a few centimeters to keep soil free from weeds. After 4 years, we measured effects of mulch application on soluble soil and microbial carbon and nitrogen in the mesocosms and compared effects of mulch application versus no mulch on soils from 0-5 cm and 5-15 cm with low and high organic matter. We predicted that mulch would increase soil carbon and nitrogen content and mulch application would have a greater effect on soils with low organic matter than soils with high organic matter. In soils with low organic carbon content and larger predicted potential to increase soil carbon, mulch application did not increase soluble soil or microbial carbon or nitrogen compared to the treatments without mulch application. However, mulch application significantly increased the δ13C of both microbial and soluble soil carbon in these soils by 1 ‰ each, indicating a shift in belowground processes, such as increased

Formation of Chromophoric Dissolved Organic Matter by Bacterial Degradation of Phytoplankton-Derived Aggregates

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Joanna D. Kinsey

2018-01-01

Full Text Available Organic matter produced and released by phytoplankton during growth is processed by heterotrophic bacterial communities that transform dissolved organic matter into biomass and recycle inorganic nutrients, fueling microbial food web interactions. Bacterial transformation of phytoplankton-derived organic matter also plays a poorly known role in the formation of chromophoric dissolved organic matter (CDOM which is ubiquitous in the ocean. Despite the importance of organic matter cycling, growth of phytoplankton and activities of heterotrophic bacterial communities are rarely measured in concert. To investigate CDOM formation mediated by microbial processing of phytoplankton-derived aggregates, we conducted growth experiments with non-axenic monocultures of three diatoms (Skeletonema grethae, Leptocylindrus hargravesii, Coscinodiscus sp. and one haptophyte (Phaeocystis globosa. Phytoplankton biomass, carbon concentrations, CDOM and base-extracted particulate organic matter (BEPOM fluorescence, along with bacterial abundance and hydrolytic enzyme activities (α-glucosidase, β-glucosidase, leucine-aminopeptidase were measured during exponential growth and stationary phase (~3–6 weeks and following 6 weeks of degradation. Incubations were performed in rotating glass bottles to keep cells suspended, promoting cell coagulation and, thus, formation of macroscopic aggregates (marine snow, more similar to surface ocean processes. Maximum carbon concentrations, enzyme activities, and BEPOM fluorescence occurred during stationary phase. Net DOC concentrations (0.19–0.46 mg C L−1 increased on the same order as open ocean concentrations. CDOM fluorescence was dominated by protein-like signals that increased throughout growth and degradation becoming increasingly humic-like, implying the production of more complex molecules from planktonic-precursors mediated by microbial processing. Our experimental results suggest that at least a portion of open

An estimation of influence of humic acid and organic matter originated from bentonite on samarium solubility

International Nuclear Information System (INIS)

Kanaji, Mariko; Sato, Haruo; Sasahira, Akira

1999-10-01

Organic acids in groundwater are considered to form complexes and increase the solubility of radionuclides released from vitrified waste in a high-level radioactive waste (HLW) repository. To investigate whether the solubility of samarium (Sm) is influenced by organic substances, we measured Sm solubility in the presence of different organic substances and compared those values with results from thermodynamic predictions. Humic acid (Aldrich) is commercially available and soluble organic matter originated from bentonite were used as organic substances in this study. Consequently, the solubility of Sm showed a tendency to apparently increase with increasing the concentration of humic acid, but in the presence of carbonate, thermodynamic predictions suggested that the dominant species are carbonate complexes and that the effect of organic substances are less than that of carbonate. Based on total organic carbon (TOC), the increase of Sm solubility measured with humic acid (Aldrich) was more significant than that in the case with soluble organic matter originated from bentonite. Since bentonite is presumed to include also simple organic matters of which stability constant for forming complexes is low, the effect of soluble organic matter originated from bentonite on the solubility of Sm is considered to be less effective than that of humic acid (Aldrich). Experimental values were compared with model prediction, proposed by Kim, based on data measured in a low pH region. Tentatively we calculated the increase in Sm solubility assuming complexation with humic acid. Trial calculations were carried out on the premise that the complexation reaction of metal ion with humic acid is based on neutralization process by 1-1 complexation. In this process, it was assumed that one metal ion coordinates with one unit of complexation sites which number of proton exchange sites is equal to ionic charge. Consequently, Kim's model indicated that carbonate complexes should be dominant

Organic, elemental and inorganic carbon in particulate matter of six urban environments in Europe

Directory of Open Access Journals (Sweden)

M. Sillanpää

2005-01-01

Full Text Available A series of 7-week sampling campaigns were conducted in urban background sites of six European cities as follows: Duisburg (autumn, Prague (winter, Amsterdam (winter, Helsinki (spring, Barcelona (spring and Athens (summer. The campaigns were scheduled to include seasons of local public health concern due to high particulate concentrations or findings in previously conducted epidemiological studies. Aerosol samples were collected in parallel with two identical virtual impactors that divide air particles into fine (PM2.5 and coarse (PM2.5-10 size ranges. From the collected filter samples, elemental (EC and organic (OC carbon contents were analysed with a thermal-optical carbon analyser (TOA; total Ca, Ti, Fe, Si, Al and K by energy dispersive X-ray fluorescence (ED-XRF; As, Cu, Ni, V, and Zn by inductively coupled plasma mass spectrometry (ICP/MS; Ca2+, succinate, malonate and oxalate by ion chromatography (IC; and the sum of levoglucosan+galactosan+mannosan (∑MA by liquid chromatography mass spectrometry (LC/MS. The campaign means of PM2.5 and PM2.5-10 were 8.3-29.6 µg m-3 and 5.4-28.7 µg m-3, respectively. The contribution of particulate organic matter (POM to PM2.5 ranged from 21% in Barcelona to 54% in Prague, while that to PM2.5-10 ranged from 10% in Barcelona to 27% in Prague. The contribution of EC was higher to PM2.5 (5-9% than to PM2.5-10 (1-6% in all the six campaigns. Carbonate (C(CO3, that interferes with the TOA analysis, was detected in PM2.5-10 of Athens and Barcelona but not elsewhere. It was subtracted from the OC by a simple integration method that was validated. The CaCO3 accounted for 55% and 11% of PM2.5-10 in Athens and Barcelona, respectively. It was anticipated that combustion emissions from vehicle engines affected the POM content in PM2.5 of all the six sampling campaigns, but a comparison of mass concentration ratios of the selected inorganic and organic tracers of common sources of organic material to POM suggested

Nature and reactivity of organic matter in argillaceous formations: example of the Callovo-Oxfordian of Bure (France)

International Nuclear Information System (INIS)

Michels, R.; Elie, M.; Faure, P.; Huault, V.; Martinez, L.; Bartier, D.; Fleck, S.; Hautevelle, Y.

2004-01-01

In carbon cycle models, it is admitted that less than 1% of produced organic carbon is transferred to the geological cycle as sedimentary organic matter (Tissot and Welte, 1984). Although, coal or petroleum source rocks are most well known, sedimentary organic matter also occurs in various concentrations throughout many different rock facies. Organic matter is therefore a witness of the record of environmental changes as well as biomass evolution through time. It is also a reliable tracer of diagenetic conditions, from sediment deposition to metamorphism and subsurface alteration. Especially in the case of argillaceous sediments, known for their potential proneness of organic matter, the study of fossil organic matter is able to unravel a large amount of information concerning the geological past (depositional conditions and preservation, paleo-environment, burial, thermal history) as well as the future (effects of induced thermal perturbation, oxidative alteration, biodegradation). We are presenting here data obtained on the Callovo-Oxfordian argillaceous formations of Bure (France), which are the target layers for the installation of a future laboratory. (authors)

Production of dissolved organic carbon in aquatic sediment suspensions

NARCIS (Netherlands)

Koelmans, A.A.; Prevo, L.

2003-01-01

In many water quality models production of dissolved organic carbon (DOC) is modelled as mineralisation from particulate organic matter (POM). In this paper it is argued that the DOC production from dessicated sediments by water turbulence may be of similar importance
In many water quality

Seasonal variations and sources of sedimentary organic carbon in Tokyo Bay

International Nuclear Information System (INIS)

Kubo, Atsushi; Kanda, Jota

2017-01-01

Total organic carbon (TOC), total nitrogen (TN) contents, their stable C and N isotope ratio (δ 13 C and δ 15 N), and chlorophyll a ([Chl a] sed ) of surface sediments were investigated monthly to identify the seasonal variations and sources of organic matter in Tokyo Bay. The sedimentary TOC (TOC sed ) and TN (TN sed ) contents, and the sedimentary δ 13 C and δ 15 N (δ 13 C sed and δ 15 N sed ) values were higher in summer than other seasons. The seasonal variations were controlled by high primary production in the water column and hypoxic water in the bottom water during summer. The fraction of terrestrial and marine derived organic matter was estimated by Bayesian mixing model using stable isotope data and TOC/TN ratio. Surface sediments in Tokyo Bay are dominated by marine derived organic matter, which accounts for about 69 ± 5% of TOC sed . - Highlights: • High values of sedimentary organic carbon and nitrogen were observed in summer. • Surface sediments in Tokyo Bay were dominated by marine derived organic matter which was estimated by Bayesian mixing model. • The most amount of terrestrial POC was deposited and degraded in Tokyo Bay before being discharged to the open ocean.

Exoenzyme activities as indicators of dissolved organic matter composition in the hyporheic zone of a floodplain river

Science.gov (United States)

Sandra M. Clinton; Rick T. Edwards; Stuart E.G. Findlay

2010-01-01

We measured the hyporheic microbial exoenzyme activities in a floodplain river to determine whether dissolved organic matter (DOM) bioavailability varied with overlying riparian vegetation patch structure or position along flowpaths. Particulate organic matter (POM), dissolved organic carbon (DOC), dissolved oxygen (DO), electrical conductivity and temperature were...

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

Transient cultivation and fallow land in forests. Measurements of the specific activity of the carbon in organic matter fractions for the purpose of studying the renewal of the store of organic matter in an equatorial forest environment

International Nuclear Information System (INIS)

Turenne, J.F.; Rapaire, J.L.

1979-01-01

Different conditions of forest-type fallow land and of clearings in the equatorial forests of the Amazon region provide a basis for determining the nature, the direction and the magnitude of the transformations of the organic matter of the soil when cultivated, using the variations in the specific activity of atmospheric carbon. Calculations of the renewal rates of surface horizon organic matter show that there are two groups of products, (a) humin, a labile fraction with a high renewal rate, and (b) humic and fulvic products with a lower renewal rate. The effect of clearing is generally to retard these renewal rates. The dynamics which become established in forest fallow land mainly involve the fulvic products, and the return to forest equilibrium can be considered to occur between 60 and 100 years after clearing. (author)

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.

The role of fossil organic matter in the ecosystem development of post-mining sites revealed by isotope analyses

Science.gov (United States)

Jandova, Katerina; Hyodo, Fujio; Vindušková, Olga; Moradi, Jabbar; Frouz, Jan

2017-04-01

Sediments rich in kerogen ( 19 Ma old, 14C-free) are present in the overburden at post-mining area in Western Bohemia, near Sokolov city, the Czech Republic. There are two successional chronosequences, an alder reclamation and spontaneous succession, consisting of sites that differ in time since heaping. Both chronosequences accumulate recent organic matter over time, although the process is initially faster at reclamation. We hypothesized that (i) radiocarbon age of soil organic matter would be decreasing with time since spoil heaping; (ii) the detrital food web would show the assimilation of fossil carbon by heterotrophic organisms in the initial stages of succession when fossil organic matter is the predominant source of carbon; (iii) the isotopic track of fossil organic matter in the detrital food web would be more prominent at sites with lower vegetation cover and litter production. Nitrogen isotopic ratios of soils were high at the young sites and the decrease in δ15N was correlated with the increase in content of recent organic carbon. Nitrogen isotopic ratios of soil detritivores equalled to that of tree leaves at reclamation but were higher at successional sites. Possibly, other food sources were used apart from tree leaves litter at the latter. Interestingly, soil animals but not primary producers were 14C depleted in the youngest relative to the oldest sites. The depletion in 14C of detritivores relative to primary producers was likely due to the geophagy behaviour of the millipedes at the young sites where fossil organic matter is the largest carbon pool.

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

Effect of Carbonates and Bivalent Cations and Their Relationships with Soil Organic Matter from the View Point of Aggregate Formation

Directory of Open Access Journals (Sweden)

Vladimír Šimanský

2014-12-01

Full Text Available The effect of carbonates on soil structure has not been sufficiently studied yet, despite the fact that in the literature their positive impact is mentioned mostly. Carbonates are the source of bivalent cations in soil solution and may be involved in stabilization of the aggregates, because negatively charged organic materials can be adsorbed onto the surface of clay by bivalent or polyvalent cations. We studied the effect of carbonates and bivalent cations and their relationships with soil organic matter (SOM from the point of view of aggregate formation. The studies were carried out in several fields located on loamy Calcaric Chernozem, loamy Haplic and Mollic Fluvisols. The results showed that between exchangeable Mg2+ and water-stable macro-aggregates (WSAma in size fractions >2 mm, positive correlations were found; however, the content of Mg2+ negative correlated with the contents of WSAma in 2 mm; however, between SBC as well as CEC and smaller size fractions of WSAma >1 mm and WSAmi negative correlations were observed. Statistically significant negative correlations were observed between SOM content in WSA and carbonate content, and this effect was stronger in relation to the labile carbon. There were also positive correlations between SOM in WSA and SBC and CEC found if all loamy soils were assessed together.

Thermodynamic constrains on the flux of organic matter through a peatland ecosystem

Science.gov (United States)

Worrall, Fred; Moody, Catherine; Clay, Gareth; Kettridge, Nick; Burt, Tim

2017-04-01

The transformations and transitions of organic matter into, through and out of a peatland ecosystem must obey the 2nd law of thermodynamics. Beer and Blodau (Geochimica Cosmochimica Acta, 2007, 71, 12, 2989-3002) showed that the evolution of CH4 in peatlands was constrained by equilibrium occurring at depth in the peat as the pore water became a closed system. However, that study did not consider the transition in the solid components of the organic matter flux through the entire ecosystem. For this study, organic matter samples were taken from each organic matter reservoir and fluvial transfer pathway and analysed the samples by elemental analysis and bomb calorimetry. The samples analysed were: above- and below-ground biomass, heather, mosses, sedges, plant litter layer, peat soil, and monthly samples of particulate and dissolved organic matter. All organic matter samples were taken from a 100% peat catchment within Moor House National Nature Reserve in the North Pennines, UK, and collected samples were compared to standards of lignin, cellulose, and plant protein. It was possible to calculate ∆H_f^OM ∆S_f^OM and ∆G_f^OM for each of the samples and standards. By assuming that each thermodynamic property can be expressed per g C and that any increase in ∆G_f^OM can be balanced by the production of CO2, DOM or CH4 then it is possible to predict the consequences of the fixation of 1 g of carbon in a peatland soil. The value of ∆G_f^OMincreases from glucose to components of the biomass: 1g of C fixed as glucose by photosynthesis would result in 0.68 g C as biomass and 0.32 g C as CO2. The transition from biomass to litter could occur spontaneously but the transition from surface to 1m depth in the peat profile would release 0.18 g C as CO2 per 1 g of carbon entering the peat profile. Therefore, for every 1 g of carbon fixed from photosynthesis then 0.44g of C would be released as CO2 and 0.54 g C would be present at 1 m depth. Alternatively, if DOM only

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 ...

Dynamics of dissolved organic matter in fjord ecosystems: Contributions of terrestrial dissolved organic matter in the deep layer

Science.gov (United States)

Yamashita, Youhei; McCallister, S. Leigh; Koch, Boris P.; Gonsior, Michael; Jaffé, Rudolf

2015-06-01

Annually, rivers and inland water systems deliver a significant amount of terrestrial organic matter (OM) to the adjacent coastal ocean in both particulate and dissolved forms; however, the metabolic and biogeochemical transformations of OM during its seaward transport remains one of the least understood components of the global carbon cycle. This transfer of terrestrial carbon to marine ecosystems is crucial in maintaining trophic dynamics in coastal areas and critical in global carbon cycling. Although coastal regions have been proposed as important sinks for exported terrestrial materials, most of the global carbon cycling data, have not included fjords in their budgets. Here we present distributional patterns on the quantity and quality of dissolved OM in Fiordland National Park, New Zealand. Specifically, we describe carbon dynamics under diverse environmental settings based on dissolved organic carbon (DOC) depth profiles, oxygen concentrations, optical properties (fluorescence) and stable carbon isotopes. We illustrate a distinct change in the character of DOC in deep waters compared to surface and mid-depth waters. Our results suggest that, both, microbial reworking of terrestrially derived plant detritus and subsequent desorption of DOC from its particulate counterpart (as verified in a desorption experiment) are the main sources of the humic-like enriched DOC in the deep basins of the studied fjords. While it has been suggested that short transit times and protection of OM by mineral sorption may ultimately result in significant terrestrial carbon burial and preservation in fjords, our data suggests the existence of an additional source of terrestrial OM in the form of DOC generated in deep, fjord water.

Repeated application of organic waste affects soil organic matter composition

DEFF Research Database (Denmark)

Peltre, Clément; Gregorich, Edward G.; Bruun, Sander

2017-01-01

Land application of organic waste is an important alternative to landfilling and incineration because it helps restore soil fertility and has environmental and agronomic benefits. These benefits may be related to the biochemical composition of the waste, which can result in the accumulation...... of different types of carbon compounds in soil. The objective of this study was to identify and characterise changes in soil organic matter (SOM) composition after repeated applications of organic waste. Soil from the CRUCIAL field experiment in Denmark was sampled after 12 years of annual application...... that there was accumulation in soil of different C compounds for the different types of applied organic waste, which appeared to be related to the degree to which microbial activity was stimulated and the type of microbial communities applied with the wastes or associated with the decomposition of applied wastes...

Extractability of water-soluble soil organic matter as monitored by spectroscopic and chromatographic analyses.

Science.gov (United States)

Nkhili, Ezzhora; Guyot, Ghislain; Vassal, Nathalie; Richard, Claire

2012-07-01

Cold and hot water processes have been intensively used to recover soil organic matter, but the effect of extraction conditions on the composition of the extracts were not well investigated. Our objective was to optimize the extraction conditions (time and temperature) to increase the extracted carbon efficiency while minimizing the possible alteration of water extractable organic matter of soil (WEOM). WEOM were extracted at 20°C, 60°C, or 80°C for 24 h, 10-60 min, and 20 min, respectively. The different processes were compared in terms of pH of suspensions, yield of organic carbon, spectroscopic properties (ultraviolet-visible absorption and fluorescence), and by chromatographic analyses. For extraction at 60°C, the time 30 min was optimal in terms of yield of organic carbon extracted and concentration of absorbing and fluorescent species. The comparison of WEOM 20°C, 24 h; 60°C, 30 min; and 80°C, 20 min highlighted significant differences. The content of total organic carbon, the value of specific ultraviolet absorbance (SUVA(254)), the absorbance ratio at 254 and 365 nm (E (2)/E (3)), and the humification index varied in the order: WEOM (20°C, 24 h) < WEOM (80°C, 20 min) < WEOM (60°C, 30 min). The three WEOM contained common fluorophores associated with simple aromatic structures and/or fulvic-like and common peaks of distinct polarity as detected by ultra performance liquid chromatography. For the soil chosen, extraction at 60°C for 30 min is the best procedure for enrichment in organic chemicals and minimal alteration of the organic matter.

Evidence of micropore filling for sorption of nonpolar organic contaminants by condensed organic matter.

Science.gov (United States)

Ran, Yong; Yang, Yu; Xing, Baoshan; Pignatello, Joseph J; Kwon, Seokjoo; Su, Wei; Zhou, Li

2013-01-01

Although microporosity and surface area of natural organic matter (NOM) are crucial for mechanistic evaluation of the sorption process for nonpolar organic contaminants (NOCs), they have been underestimated by the N adsorption technique. We investigated the CO-derived internal hydrophobic microporosity () and specific surface area (SSA) obtained on dry samples and related them to sorption behaviors of NOCs in water for a wide range of condensed NOM samples. The is obtained from the total CO-derived microporosity by subtracting out the contribution of the outer surfaces of minerals and NOM using N adsorption-derived parameters. The correlation between or CO-SSA and fractional organic carbon content () is very significant, demonstrating that much of the microporosity is associated with internal NOM matrices. The average and CO-SSA are, respectively, 75.1 μL g organic carbon (OC) and 185 m g OC from the correlation analysis. The rigid aliphatic carbon significantly contributes to the microporosity of the Pahokee peat. A strong linear correlation is demonstrated between / and the OC-normalized sorption capacity at the liquid or subcooled liquid-state water solubility calculated via the Freundlich equation for each of four NOCs (phenanthrene, naphthalene, 1,3,5-trichlorobenzene, and 1,2-dichlorobenzene). We concluded that micropore filling ("adsorption") contributes to NOC sorption by condensed NOM, but the exact contribution requires knowing the relationship between the dry-state, CO-determined microporosity and the wet-state, NOC-available microporosity of the organic matter. The findings offer new clues for explaining the nonideal sorption behaviors of NOCs. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

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

Science.gov (United States)

F.S. Peterson; K. Lajtha

2013-01-01

Factors influencing soil organic matter (SOM) stabilization and dissolved organic carbon (DOC) content in complex terrain, where vegetation, climate, and topography vary over the scale of a few meters, are not well understood. We examined the spatial correlations of lidar and geographic information system-derived landscape topography, empirically measured soil...

Role of organic matter in uranium mineralisation in Vempalle dolostone; Cuddapah basin, India

International Nuclear Information System (INIS)

Goswami, Sukanta; Bhagat, Sangeeta; Zakaulla, Syed; Kumar, Suresh; Rai, A.K.

2017-01-01

Dolostone of Vempalle Formation near Tummalapalle hosts large uranium deposit (>100,000 tonnes with an average grade of 0.045% U_3O_8). It is a unique type of uranium deposit because carbonate formations have been considered to be among the least uraniferous of all the rocks of the Earth's crust due to mobility of uranium in aqueous fluid in the presence of carbonate and bicarbonate ions. Vempalle dolostone hosts syn-sedimentary uranium mineralization in the form of discrete uranium phases (pitchblende and coffinite) associated with collophane, and adsorbed uranium in organic matter. The organic matter has played dual role of concentrating uranium from solution and also chemically reducing it to pitchhblende and coffinite. (author)

Study of Organic Matter in Soils of the Amazon Region Employing Laser Induced Fluorescence Spectroscopy

Science.gov (United States)

Tadini, Amanda Maria; Nicolodelli, Gustavo; Mounier, Stéphane; Montes, Célia Regina; Marcondes Bastos Pereira Milori, Débora

2014-05-01

In the face of climate change and increasing CO2 levels in the atmosphere, the global carbon cycle, soil organic carbon (SOC) sequestration, and the role of different world biomes as potential sources and sinks of carbon are receiving increasing attention. Carbon quantification is an important environmental indicator, but the structure of organic matter is also important because is related to carbon stability. The synthesis of soil organic matter (SOM), as presented in soils of forest vegetation, can be originated from condensation polymeric polyphenols and quinones that are responsible for controlling the main physical-chemical properties of soils. These systems are present in humic substances, representing the major fluorophore of SOM[1-3]. Abiotic factors, such as soil texture, use and occupation of soil, can influence on the process of SOM formation, molecular structure and in its humification index[4]. Laser Induced Fluorescence Spectroscopy (LIFS) have become a promising technique for assessing humification index of SOM (HLIFS). In this context, the aim of this study was to analyze the humification index of the SOM in the region of Barcelos (Amazon) employing LIFS. The study area was the region of Barcelos, close the river Demeni. The whose vegetation distribution in this area, is two biomes the Dense Ombrophylous Forest (DPQD) and Campinarana (DPQT), with areas of edaphic contacts between these two phytophysiognomies, which ranged from Open field (FDE) to closed Depression (DPQ). Preliminary results showed that the area closed Depression (DPQ) there was a continuous gradient of humification with increasing soil depth. A similar behavior was verified for area Forest (DPQD), where the highest values of HLIFS were obtained between the four points analyzed, indicating the magnitude of the molecular recalcitrance this organic matter in this area. The results obtained for area Campinarana (DPQT) and Open field (FDE) showed an opposite behavior. These points there

Assessment of relative accuracy in the determination of organic matter concentrations in aquatic systems

Science.gov (United States)

Aiken, G.; Kaplan, L.A.; Weishaar, J.

2002-01-01

Accurate determinations of total (TOC), dissolved (DOC) and particulate (POC) organic carbon concentrations are critical for understanding the geochemical, environmental, and ecological roles of aquatic organic matter. Of particular significance for the drinking water industry, TOC measurements are the basis for compliance with US EPA regulations. The results of an interlaboratory comparison designed to identify problems associated with the determination of organic matter concentrations in drinking water supplies are presented. The study involved 31 laboratories and a variety of commercially available analytical instruments. All participating laboratories performed well on samples of potassium hydrogen phthalate (KHP), a compound commonly used as a standard in carbon analysis. However, problems associated with the oxidation of difficult to oxidize compounds, such as dodecylbenzene sulfonic acid and caffeine, were noted. Humic substances posed fewer problems for analysts. Particulate organic matter (POM) in the form of polystyrene beads, freeze-dried bacteria and pulverized leaf material were the most difficult for all analysts, with a wide range of performances reported. The POM results indicate that the methods surveyed in this study are inappropriate for the accurate determination of POC and TOC concentration. Finally, several analysts had difficulty in efficiently separating inorganic carbon from KHP solutions, thereby biasing DOC results.

Soil mineral assemblage influences on microbial communities and carbon cycling under fresh organic matter input

Science.gov (United States)

Finley, B. K.; Schwartz, E.; Koch, B.; Dijkstra, P.; Hungate, B. A.

2017-12-01

The interactions between soil mineral assemblages and microbial communities are important drivers of soil organic carbon (SOC) cycling and storage, although the mechanisms driving these interactions remain unclear. There is increasing evidence supporting the importance of associations with poorly crystalline, short-range order (SRO) minerals in protection of SOC from microbial utilization. However, how the microbial processing of SRO-associated SOC may be influenced by fresh organic matter inputs (priming) remains poorly understood. The influence on SRO minerals on soil microbial community dynamics is uncertain as well. Therefore, we conducted a priming incubation by adding either a simulated root exudate mixture or conifer needle litter to three soils from a mixed-conifer ecosystem. The parent material of the soils were andesite, basalt, and granite and decreased in SRO mineral content, respectively. We also conducted a parallel quantitative stable isotope probing incubation by adding 18O-labelled water to the soils to isotopically label microbial DNA in situ. This allowed us to characterize and identify the active bacterial and archaeal community and taxon-specific growth under fresh organic matter input. While the granite soil (lowest SRO content), had the largest total mineralization, the least priming occurred. The andesite and basalt soils (greater SRO content) had lower total respiration, but greater priming. Across all treatments, the granite soil, while having the lowest species richness of the entire community (249 taxa, both active and inactive), had a larger active community (90%) in response to new SOC input. The andesite and basalt soils, while having greater total species richness of the entire community at 333 and 325 taxa, respectively, had fewer active taxa in response to new C compared to the granite soil (30% and 49% taxa, respectively). These findings suggest that the soil mineral assemblage is an important driver on SOC cycling under fresh

Reactivity of Organic Matter and other Reductants in Aquifer Sediments

NARCIS (Netherlands)

Hartog, N.

2003-01-01

The molecular composition and the carbon isotope signature of sedimentary organic matter (SOM) and indicate that SOM is predominantly derived from higher land plants in sediments of both terrestrial as marine origins. The reactivity of SOM in the aquifer sediments studied is determined by the extent

Relationship between the colored dissolved organic matter and dissolved organic carbon and the application on remote sensing in East China Sea

Science.gov (United States)

Qiong, Liu; Pan, Delu; Huang, Haiqing; Lu, Jianxin; Zhu, Qiankun

2011-11-01

A cruise was conducted in the East China Sea (ECS) in autumn 2010 to collect Dissolved Organic Carbon (DOC) and Colored Dissolved Organic Matter (CDOM) samples. The distribution of DOC mainly controlled by the hydrography since the relationship between DOC and salinity was significant in both East China Sea. The biological activity had a significant influence on the concentration of DOC with a close correlation between DOC and Chl a. The absorption coefficient of CDOM (a355) decreased with the salinity increasing in the shelf of East China Sea (R2=0.9045). CDOM and DOC were significantly correlated in ECS where DOC distribution was dominated largely by the Changjiang diluted water. Based on the relationship of CDOM and DOC, we estimated the DOC concentration of the surface in ECS from satellite-derived CDOM images. Some deviations induced by the biological effect and related marine DOC accumulations were discussed.

Refractory organic matter in coastal salt marshes-effect on C sequestration calculations.

Science.gov (United States)

Leorri, Eduardo; Zimmerman, Andrew R; Mitra, Siddhartha; Christian, Robert R; Fatela, Francisco; Mallinson, David J

2018-08-15

The age and ability of salt marshes to accumulate and sequester carbon is often assessed using the carbon isotopic signatures (Δ 14 C and δ 13 C) of sedimentary organic matter. However, transfers of allochthonous refractory carbon (C RF ) from the watershed to marshes would not represent new C sequestration. To better understand how refractory carbon (C RF ) inputs affect assessments of marsh age and C sequestration, Δ 14 C and δ 13 C of both total organic carbon (TOC), C RF , and non-C RF organic matter fractions were measured in salt marshes from four contrasting systems on the North Atlantic coast. To our knowledge, no salt marsh sediment study has considered refractory or allochthonous carbon in carbon budget calculations or the impact on chronologies. Stable and radiogenic isotope data suggest that while TOC was dominated by autochthonous plant inputs, C RF was dominated by locally recycled or allochthonous C, the delivery of which was controlled by the size and slope of each watershed. Steep-gradient rivers analyzed delivered Δ 14 C-depleted C RF to their estuarine marshes, while the site located in the low-gradient river was associated with larger C RF content. Finally, the marsh isolated from riverine input contained the least fraction of TOC as C RF . Laterally transported C RF caused only a small offset in Δ 14 C in relation to TOC in low-gradient systems (average Δ 14 C offset was -44.4 and -24.2‰ at each location). However, the presence of allochthonous Δ 14 C-depleted C RF in sediments of steep-gradient rivers led to large overestimates of the time of organic matter deposition (i.e. apparent age was older than the 'true' time of deposition) (Δ 14 C offset ranged from -170.6 to -528.9‰). Further, reliance on TOC or loss on ignition analyses to calculate C sequestration by marshes might produce overestimates of at least as much as 10 to 20% since neither account for the lateral transport of allochthonous carbon. Copyright © 2018 Elsevier B

Impact of sediment organic matter quality on the fate and effects of fluoranthene in the infaunal brittle star Amphiura filiformis

DEFF Research Database (Denmark)

Selck, Henriette; Granberg, Maria E; Forbes, Valery E.

2005-01-01

Hydrophobic contaminants, such as polycyclic aromatic hydrocarbons (PAHs) readily adsorb to organic matter. The aim of this study was to determine the importance of the quality of sedimentary organic matter for the uptake, biotransformation and toxicity of the PAH, fluoranthene (Flu......), in the infaunal brittle star Amphiura filiformis. Brittle stars were exposed to a base sediment covered by a 2 cm Flu-spiked top layer (30 mug Flu/g dry wt. sed.), enriched to the same total organic carbon content with either refractory or labile organic matter. The labile carbon source was concentrated green...... to equilibrium partitioning between organism lipid content and organic content of the sediment. Biotransformation of Flu by brittle stars was very limited and unaffected by organic matter quality. A. filiformis contributed to the downward transport of Flu from the surface sediment to the burrow lining...

Including Effects of Water Stress on Dead Organic Matter Decay to a Forest Carbon Model

Science.gov (United States)

Kim, H.; Lee, J.; Han, S. H.; Kim, S.; Son, Y.

2017-12-01

Decay of dead organic matter is a key process of carbon (C) cycling in forest ecosystems. The change in decay rate depends on temperature sensitivity and moisture conditions. The Forest Biomass and Dead organic matter Carbon (FBDC) model includes a decay sub-model considering temperature sensitivity, yet does not consider moisture conditions as drivers of the decay rate change. This study aimed to improve the FBDC model by including a water stress function to the decay sub-model. Also, soil C sequestration under climate change with the FBDC model including the water stress function was simulated. The water stress functions were determined with data from decomposition study on Quercus variabilis forests and Pinus densiflora forests of Korea, and adjustment parameters of the functions were determined for both species. The water stress functions were based on the ratio of precipitation to potential evapotranspiration. Including the water stress function increased the explained variances of the decay rate by 19% for the Q. variabilis forests and 7% for the P. densiflora forests, respectively. The increase of the explained variances resulted from large difference in temperature range and precipitation range across the decomposition study plots. During the period of experiment, the mean annual temperature range was less than 3°C, while the annual precipitation ranged from 720mm to 1466mm. Application of the water stress functions to the FBDC model constrained increasing trend of temperature sensitivity under climate change, and thus increased the model-estimated soil C sequestration (Mg C ha-1) by 6.6 for the Q. variabilis forests and by 3.1 for the P. densiflora forests, respectively. The addition of water stress functions increased reliability of the decay rate estimation and could contribute to reducing the bias in estimating soil C sequestration under varying moisture condition. Acknowledgement: This study was supported by Korea Forest Service (2017044B10-1719-BB01)

Comprehensive characterization of atmospheric organic matter in Fresno, California fog water.

Science.gov (United States)

Herckes, Pierre; Leenheer, Jerry A; Collett, Jeffrey L

2007-01-15

Fogwater collected during winter in Fresno (CA) was characterized by isolating several distinct fractions and characterizing them by infrared and nuclear magnetic resonance (NMR) spectroscopy. More than 80% of the organic matter in the fogwater was recovered and characterized. The most abundant isolated fractions were those comprised of volatile acids (24% of isolated carbon) and hydrophilic acids plus neutrals (28%). Volatile acids, including formic and acetic acid, have been previously identified as among the most abundant individual species in fogwater. Recovered hydrophobic acids exhibited some properties similar to aquatic fulvic acids. An insoluble particulate organic matter fraction contained a substantial amount of biological material, while hydrophilic and transphilic fractions also contained material suggestive of biotic origin. Together, these fractions illustrate the important contribution biological sources make to organic matter in atmospheric fog droplets. The fogwater also was notable for containing a large amount of organic nitrogen present in a variety of species, including amines, nitrate esters, peptides, and nitroso compounds.

Soil Organic Carbon in the Soil Scapes of Southeastern Tanzania

OpenAIRE

Rossi, Joni

2009-01-01

Soil organic carbon (SOC) is well known to maintain several functions. On the one hand, being the major component of soil organic matter (SOM),it is a determinant of soil physical and chemical properties, an important proxy for soil biological activity and a measure of soil productivity. Land use management that will enhance soil carbon (C) levels is therefore important for farmers and land use planners, particularly in semiarid and sub-humid Africa where severe soil degradation and desertifi...

Heterogeneity of the organic matter in the Guayuta group, Eastern Venezuelan Basin

Energy Technology Data Exchange (ETDEWEB)

Alberdi, M.; Gallango, O.; Ruggiero, A.; Jordan, N. (Intevep, S.A., Caracas (Venezuela)); Lefargue, E. (I.F.P., Rueil Malmaison (France))

1993-02-01

The purpose of this study is to evaluate the organic matter heterogeneities in the Guayuta Group as a principal hydrocarbon source rock in the Eastern Venezuelan Basin. In order to do this, thirteen wells and five work stations on outcrops of the Interior Mountain Belt were analyzed to study the regional and vertical variations in the geochemical characteristics of the organic matter. It is possible to detect significant differences in quality and quantity of the organic matter which could corroborate the regional development of two organic facies from North to South in the Maturin Subbasin. The northern organic facies show excellent characteristics as source rock. The study of vertical distribution of organic matter was carried out in a well of northern part of the Monagas state, which represents the southern organic facies. It shows an irregular input of continental organic matter, thermally immature. Besides the organic matter content was low (around 1.5%) without depth tendencies. These sediments are clastic and bioclastic in contrast with carbonates and pelagic shales of the Guayuta Group in the Interior Mountain Belt. The outcrop samples studied show a high total organic content (2-6%) despite the high maturity determined on kerogen. The systematic study of this geochemical parameter show pseudocyclic relationships with a general tendency to increase toward the bottom of the section. V, Ni, and S determinations could indicate that anoxic conditions were developing toward the North where the marine organic matter was sedimenting. The results of this study are in agreement with paleogeographic model of sedimentation during middle and late Cretaceous, with sources of sediments from South and a progressive depth of the basin toward the North.

Long-term changes in primary production and mineralization of organic matter in the Neva Estuary (Baltic Sea)

Science.gov (United States)

Golubkov, Sergey; Golubkov, Mikhail; Tiunov, Alexei; Nikulina, Vera

2017-07-01

The Neva Estuary situated in the eastern part of the Gulf of Finland is one of the largest estuaries of the Baltic Sea. At present, heavy nutrient and organic matter loading, mainly from the Neva River and point sources in the upper estuary are the most serious environmental problem for the Neva Estuary and adjacent parts of the eastern Gulf of Finland. Long-term studies of mid-summer primary production and mineralization of organic matter were conducted in upper and middle parts of the Neva Estuary. A considerable increase of production and biomass of phytoplankton was observed in the middle part of the estuary during the last decades mainly due to an increase in biomass of cyanobacteria. However, they are mostly concentrated in the upper water layers and only a small part of them reached the near bottom water layers and may be used as a food by zoobenthos. The mineralization of organic matter in the water column was twice higher than primary production that indicates the importance of allochthonous organic matter in the carbon budget of the both parts of the estuary. The carbon isotope signature of seston and most of the zoobenthic species in the upper part of the estuary was close to the signature of allochthonous carbon leaking from watershed (- 27‰). Higher values of δ13C of seston in the upper mix layer of the Middle estuary indicate intensive primary production in mid-summer. The carbon isotopic signature of zoobenthos in this part of the estuary was also in general lower than in the Neva Bay reflected higher importance of autochthonous organic matter in food webs of the estuary.

Hyphenation of a carbon analyzer to photo-ionization mass spectrometry to unravel the organic composition of particulate matter on a molecular level.

Science.gov (United States)

Grabowsky, Jana; Streibel, Thorsten; Sklorz, Martin; Chow, Judith C; Watson, John G; Mamakos, Athanasios; Zimmermann, Ralf

2011-12-01

The carbonaceous fraction of airborne particulate matter (PM) is of increasing interest due to the adverse health effects they are linked to. Its analytical ascertainment on a molecular level is still challenging. Hence, analysis of carbonaceous fractions is often carried out by determining bulk parameters such as the overall content of organic compounds (OC) and elemental carbon (EC) as well as the total carbon content, TC (sum of OC and EC), however, no information about the individual substances or substance classes, of which the single fractions consist can be obtained. In this work, a carbon analyzer and a photo-ionization time-of-flight mass spectrometer (PI-TOF-MS) were hyphenated to investigate individual compounds especially from the OC fractions. The carbon analyzer enables the stepwise heating of particle samples and provides the bulk parameters. With the PI-TOF-MS, it is possible to detect the organic compounds released during the single-temperature steps due to soft ionization and fast detection of the molecular ions. The hyphenation was designed, built up, characterized by standard substances, and applied to several kinds of samples, such as ambient aerosol, gasoline, and diesel emission as well as wood combustion emission samples. The ambient filter sample showed a strong impact of wood combustion markers. This was revealed by comparison to the product pattern of the similar analysis of pure cellulose and lignin and the wood combustion PM. At higher temperatures (450 °C), a shift to smaller molecules occurred due to the thermal decomposition of larger structures of oligomeric or polymeric nature comparable to lignocelluloses and similar oxygenated humic-like substances. Finally, particulate matter from gasoline and diesel containing 10% biodiesel vehicle exhaust has been analyzed. Gasoline-derived PM exhibited large polycyclic aromatic hydrocarbons, whereas diesel PM showed a much higher total organic content. The detected pattern revealed a strong

Characterization of dissolved organic matter during landfill leachate treatment by sequencing batch reactor, aeration corrosive cell-Fenton, and granular activated carbon in series

International Nuclear Information System (INIS)

Bu Lin; Wang Kun; Zhao Qingliang; Wei Liangliang; Zhang Jing; Yang Junchen

2010-01-01

Landfill leachate is generally characterized as a complex recalcitrant wastewater containing high concentration of dissolved organic matter (DOM). A combination of sequencing batch reactor (SBR) + aeration corrosive cell-Fenton (ACF) + granular activated carbon (GAC) adsorption in series was proposed for the purpose of removing pollutants in the leachate. Fractionation was also performed to investigate the composition changes and characteristics of the leachate DOM in each treatment process. Experimental results showed that organic matter, in terms of chemical oxygen demand (COD), 5-day biological oxygen demand (BOD 5 ), and dissolved organic carbon (DOC), was reduced by 97.2%, 99.1%, and 98.7%, respectively. To differentiate the DOM portions, leachates were separated into five fractions by XAD-8 and XAD-4 resins: hydrophobic acid (HPO-A), hydrophobic neutral (HPO-N), transphilic acid (TPI-A), transphilic neutral (TPI-N), and hydrophilic fraction (HPI). The predominant fraction in the raw leachate was HPO-A (36% of DOC), while the dominant fraction in the final effluent was HPI (53% of DOC). Accordingly, macromolecules were degraded to simpler ones in a relatively narrow range below 1000 Da. Spectral and chromatographic analyses also showed that most humic-like substances in all fractions were effectively removed during the treatments and led to a simultaneous decrease in aromaticity.

Characterization of dissolved organic matter during landfill leachate treatment by sequencing batch reactor, aeration corrosive cell-Fenton, and granular activated carbon in series

Energy Technology Data Exchange (ETDEWEB)

Bu Lin [School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin 150090 (China); Wang Kun [State Key Laboratory of Urban Water Resources and Environment (SKLUWRE), Harbin Institute of Technology, Harbin 150090 (China); School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin 150090 (China); Zhao Qingliang, E-mail: zhql1962@yahoo.com.cn [State Key Laboratory of Urban Water Resources and Environment (SKLUWRE), Harbin Institute of Technology, Harbin 150090 (China); School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin 150090 (China); Wei Liangliang; Zhang Jing; Yang Junchen [School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin 150090 (China)

2010-07-15

Landfill leachate is generally characterized as a complex recalcitrant wastewater containing high concentration of dissolved organic matter (DOM). A combination of sequencing batch reactor (SBR) + aeration corrosive cell-Fenton (ACF) + granular activated carbon (GAC) adsorption in series was proposed for the purpose of removing pollutants in the leachate. Fractionation was also performed to investigate the composition changes and characteristics of the leachate DOM in each treatment process. Experimental results showed that organic matter, in terms of chemical oxygen demand (COD), 5-day biological oxygen demand (BOD{sub 5}), and dissolved organic carbon (DOC), was reduced by 97.2%, 99.1%, and 98.7%, respectively. To differentiate the DOM portions, leachates were separated into five fractions by XAD-8 and XAD-4 resins: hydrophobic acid (HPO-A), hydrophobic neutral (HPO-N), transphilic acid (TPI-A), transphilic neutral (TPI-N), and hydrophilic fraction (HPI). The predominant fraction in the raw leachate was HPO-A (36% of DOC), while the dominant fraction in the final effluent was HPI (53% of DOC). Accordingly, macromolecules were degraded to simpler ones in a relatively narrow range below 1000 Da. Spectral and chromatographic analyses also showed that most humic-like substances in all fractions were effectively removed during the treatments and led to a simultaneous decrease in aromaticity.

Assessment of Soil Organic Carbon Stock of Temperate Coniferous Forests in Northern Kashmir

Directory of Open Access Journals (Sweden)

Davood A. Dar

2015-02-01

Full Text Available  Soil organic carbon (SOC estimation in temperate forests of the Himalaya is important to estimate their contribution to regional, national and global carbon stocks. Physico chemical properties of soil were quantified to assess soil organic carbon density (SOC and SOC CO2 mitigation density at two soil depths (0-10 and 10-20 cms under temperate forest in the Northern region of Kashmir Himalayas India. The results indicate that conductance, moisture content, organic carbon and organic matter were significantly higher while as pH and bulk density were lower at Gulmarg forest site. SOC % was ranging from 2.31± 0.96 at Gulmarg meadow site to 2.31 ± 0.26 in Gulmarg forest site. SOC stocks in these temperate forests were from 36.39 ±15.40 to 50.09 ± 15.51 Mg C ha-1. The present study reveals that natural vegetation is the main contributor of soil quality as it maintained the soil organic carbon stock. In addition, organic matter is an important indicator of soil quality and environmental parameters such as soil moisture and soil biological activity change soil carbon sequestration potential in temperate forest ecosystems.DOI: http://dx.doi.org/10.3126/ije.v4i1.12186International Journal of Environment Volume-4, Issue-1, Dec-Feb 2014/15; page: 161-178

Role of sedimentary organic matter in bacterial sulfate reduction: the G model tested

International Nuclear Information System (INIS)

Westrich, J.T.; Berner, R.A.

1984-01-01

Laboratory study of the bacterial decomposition of Long Island Sound plankton in oxygenated seawater over a period of 2 years shows that the organic material undergoes decomposition via first-order kinetics and can be divided into two decomposable fractions, of considerably different reactivity, and a nonmetabolized fraction. This planktonic material, after undergoing varying degrees of oxic degradation, was added in the laboratory to anoxic sediment taken from a depth of 1 m at the NWC site of Long Island Sound and the rate of bacterial sulfate reduction in the sediment measured by the 35 S radiotracer technique. The stimulated rate of sulfate reduction was in direct proportion to the amount of planktonic carbon added. This provides direct confirmation of the first-order decomposition, or G model, for marine sediments and proves that the in situ rate of sulfate reduction is organic-matter limited. Slower sulfate reduction rates resulted when oxically degraded plankton rather than fresh plankton was added, and the results confirm the presence of the same two fractions of organic matter deduced from the oxic degradation studies. Near-surface Long Island Sound sediment, which already contains abundant readily decomposable organic matter, was also subjected to anoxic decomposition by bacterial sulfate reduction. The decrease in sulfate reduction rate with time parallels decreases in the amount of organic matter, and these results also indicate the presence of two fractions of organic carbon of distinctly different reactivity. From plots of the log of reduction rate vs. time two first-order rate constants were obtained that agree well with those derived from the plankton addition experiment. Together, the two experiments confirm the use of a simple multi-first-order rate law for organic matter decomposition in marine sediments

The influence of iron oxide nanoparticles upon the adsorption of organic matter on magnetic powdered activated carbon.

Science.gov (United States)

Lompe, Kim Maren; Menard, David; Barbeau, Benoit

2017-10-15

Combining powdered activated carbon (PAC) with magnetic iron oxides has been proposed in the past to produce adsorbents for natural organic matter (NOM) removal that can be easily separated using a magnetic field. However, the trade-off between the iron oxides' benefits and the reduced carbon content, porosity, and surface area has not yet been investigated systematically. We produced 3 magnetic powdered activated carbons (MPAC) with mass fractions of 10%, 38% and 54% maghemite nanoparticles and compared them to bare PAC and pure nanoparticles with respect to NOM adsorption kinetics and isotherms. While adsorption kinetics were not influenced by the presence of the iron oxide nanoparticles (IONP), as shown by calculated diffusion coefficients from the homogeneous surface diffusion model, nanoparticles reduced the adsorption capacity of NOM due to their lower adsorption capacity. Although the nanoparticles added mesoporosity to the composite materials they blocked intrinsic PAC mesopores at mass fractions >38% as measured by N 2 -adsorption isotherms. Below this mass fraction, the adsorption capacity was mainly dependent on the carbon content in MPAC and mesopore blocking was negligible. If NOM adsorption with MPAC is desired, a highly mesoporous PAC and a low IONP mass fraction should be chosen during MPAC synthesis. Copyright © 2017 Elsevier Ltd. All rights reserved.

Effects of salinity and organic matter on the partitioning of perfluoroalkyl acid (PFAs) to clay particles.

Science.gov (United States)

Jeon, Junho; Kannan, Kurunthachalam; Lim, Byung J; An, Kwang Guk; Kim, Sang Don

2011-06-01

The influence of salinity and organic matter on the distribution coefficient (K(d)) for perfluorooctane sulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) in a brackish water-clay system was studied. The distribution coefficients (K(d)) for PFAs onto inorganic clay surfaces increased with salinity, providing evidence for electrostatic interaction for the sorption of PFAs, whereas the relationship between K(d) and organic carbon content (f(oc)) suggested that hydrophobic interaction is the primary driving force for the sorption of PFAs onto organic matter. The organic carbon normalized adsorption coefficient (K(oc)) of PFAs can be slightly overestimated due to the electrostatic interaction within uncoated inorganic surfaces. In addition, the dissolved organic matter released from coated clay particles seemed to solvate PFA molecules in solution, which contributed to a decrease in K(d). A positive relationship between K(d) and salinity was apparent, but an empirical relationship for the 'salting-out' effect was not evident. The K(d) values of PFAs are relatively small compared with those reported for persistent organic pollutants. Thus, sorption may not be a significant route of mass transfer of PFAs from water columns in estuarine environments. However, enhancement of sorption of PFAs to particulate matter at high salinity values could evoke potential risks to benthic organisms in estuarine areas.

Radiocarbon enrichment of soil organic matter fractions in New Zealand soils

International Nuclear Information System (INIS)

Goh, K.M.; Stout, J.D.; Rafter, T.A.

1977-01-01

Soil organic matter was extracted using the classical procedure and fractionated into humin (nonextractable), humic acid, and fulvic acid. The masses of total organic carbon in the whole soil samples and in the fractions, together with their 14 C content and 13 C/ 12 C ratios, were also determined. The following New Zealand soils were studied: a Fluvaquent, with experimental pasture plots, formed from deeply mixing subsoils of low organic carbon content; a Typic Fragiaqualf and a Typic Dystrochrept with moderately productive pastures; and an Umbric Vitrandept at two sites under native tussock and under introduced grasses of low productivity. The degree of radiocarbon enrichment of the different fractions in both topsoil and subsoil samples was examined in relation to differences in soil type, soil biological activity, and vegetation history. There was variation in the distribution and enrichment of the organic matter fractions both within the same soil type and between soil types, as well as between the topsoil and subsoil of the same soil. Differences appeared to be primarily a function of the stage of decomposition and translocation of the fractions through the soil rather than due to vegetation differences

Modeling the vertical soil organic matter profile using Bayesian parameter estimation

NARCIS (Netherlands)

Braakhekke, M.C.; Wutzler, T.; Beer, C.; Kattge, J.; Schrumpf, M.; Schöning, I.; Hoosbeek, M.R.; Kruijt, B.; Kabat, P.

2012-01-01

The vertical distribution of soil organic matter (SOM) in the profile may constitute a significant factor for soil carbon cycling. However, the formation of the SOM profile is currently poorly understood due to equifinality, caused by the entanglement of several processes: input from roots, mixing

Modeling the vertical soil organic matter profile using Bayesian parameter estimation

NARCIS (Netherlands)

Braakhekke, M.C.; Wutzler, T.; Beer, C.; Kattge, J.; Schrumpf, M.; Ahrens, B.; Schoning, I.; Hoosbeek, M.R.; Kruijt, B.; Kabat, P.; Reichstein, M.

2013-01-01

The vertical distribution of soil organic matter (SOM) in the profile may constitute an important factor for soil carbon cycling. However, the formation of the SOM profile is currently poorly understood due to equifinality, caused by the entanglement of several processes: input from roots, mixing

Influence of management on the composition of organic matter in a red-brown earth as shown by 13C nuclear magnetic resonance

International Nuclear Information System (INIS)

Oades, J.M.; Waters, A.G.; Jones, G.P.; Vassallo, A.M.; Wilson, M.A.

1988-01-01

Samples were obtained from the same red-brown earth: in an undisturbed state, after 60 years of an exploitive wheat-fallow rotation and after 40 years under a fertilized mixed grass-legume pasture. Organic materials were concentrated in various fractions which enabled comparative chemical composition of the organic materials in the three soils by 13 C CPMAS n.m.r. spectroscopy. Despite more than twofold differences in the organic carbon content of the soils, the chemistry of the organic matter in the soils was similar, particularly organic matter associated with clay fractions. Most of the differences detected were associated with plant debris in particles > 20 μm which contained most of the aromatic carbon. The results indicate a rapid disappearance of phenolic-carbon which originates in lignins. The composition of sodium hydroxide extracts reflects quite well the composition of the organic matter in the soil. It is concluded that in a particulate soil type, changes in amount and nature of added photosynthate do not change the composition of the organic matter which is controlled by the microbial biomass and interactions of the biomass and its decomposition products with the soil matrix. Implications of this conclusion for the turnover of organic carbon in soil and stability of soil structure are discussed. 20 refs., 4 figs

Selective extraction methods for aluminium, iron and organic carbon from montane volcanic ash soils

NARCIS (Netherlands)

Jansen, B.; Tonneijck, F.H.; Verstraten, J.M.

2011-01-01

Montane volcanic ash soils contain disproportionate amounts of soil organic carbon and thereby play an often underestimated role in the global carbon cycle. Given the central role of Al and Fe in stabilizing organic matter in volcanic ash soils, we assessed various extraction methods of Al, Fe, and

ORGANIC MATTER FRACTIONS OF AN IRRIGATED OXISOL UNDER NO - TILL AND CONVENTIONAL TILLAGE IN THE BRAZILIAN SEMI - ARID REGION

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RAFAEL PEREIRA SALES

2017-01-01

Full Text Available The replacement of natural vegetation by crop systems directly impacts the soil organic matter fractions. The objective of this study was to evaluate the total organic carbon (TOC and nitrogen (TN contents in different fractions of the soil organic matter (SOM of an Oxisol of the Brazilian semiarid region under different irrigated crops and different soil management systems. Seven treatments were evaluated, which consisted of two soil management systems (no - till and conventional tillage and three crops (maize, sunflower and sorghum, using as reference the soil under a native forest (NF. The summer crops preceded common bean crops in the autumn - winter. The total organic carbon content, total nitrogen, carbon content in humic substances and their constituents (fulvic acids, humic acids and humin and labile, non - labile and water - soluble carbon contents were evaluated two years and three months after the experiment implementation to determine the carbon lability (L lability index (LI, partitioning index (CPI and management index (CMI. The greatest carbon, nitrogen and organic matter contents in the soil surface layer (0.00 - 0.05 m were found in crops under no - till system (NTS, especially maize. The crops under NTS presented greater carbon content in humic substances than the conventional tillage system (CTS ones in the layer 0.05 - 0.10 m. The crops under NTS presented greater sustainability in the Brazilian semiarid region compared with those under CTS, as shown by their higher CMI in the soil surface layer.

Soil type-depending effect of paddy management: composition and distribution of soil organic matter

Science.gov (United States)

Urbanski, Livia; Kölbl, Angelika; Lehndorff, Eva; Houtermans, Miriam; Schad, Peter; Zhang, Gang-Lin; Rahayu Utami, Sri; Kögel-Knabner, Ingrid

2016-04-01

Paddy soil management is assumed to promote soil organic matter accumulation and specifically lignin caused by the resistance of the aromatic lignin structure against biodegradation under anaerobic conditions during inundation of paddy fields. The present study investigates the effect of paddy soil management on soil organic matter composition compared to agricultural soils which are not used for rice production (non-paddy soils). A variety of major soil types, were chosen in Indonesia (Java), including Alisol, Andosol and Vertisol sites (humid tropical climate of Java, Indonesia) and in China Alisol sites (humid subtropical climate, Nanjing). This soils are typically used for rice cultivation and represent a large range of soil properties to be expected in Asian paddy fields. All topsoils were analysed for their soil organic matter composition by solid-state 13C nuclear magnetic resonance spectroscopy and lignin-derived phenols by CuO oxidation method. The soil organic matter composition, revealed by solid-state 13C nuclear magnetic resonance, was similar for the above named different parent soil types (non-paddy soils) and was also not affected by the specific paddy soil management. The contribution of lignin-related carbon groups to total SOM was similar in the investigated paddy and non-paddy soils. A significant proportion of the total aromatic carbon in some paddy and non-paddy soils was attributed to the application of charcoal as a common management practise. The extraction of lignin-derived phenols revealed low VSC (vanillyl, syringyl, cinnamyl) values for all investigated soils, being typical for agricultural soils. An inherent accumulation of lignin-derived phenols due to paddy management was not found. Lignin-derived phenols seem to be soil type-dependent, shown by different VSC concentrations between the parent soil types. The specific paddy management only affects the lignin-derived phenols in Andosol-derived paddy soils which are characterized by

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

International Nuclear Information System (INIS)

Schmoker, J.W.

1981-01-01

The organic-matter content of the Devonian shale of the Appalachian basin is important for assessing the natural-gas resources of these rocks, and patterns of organic-matter distribution convey information on sedimentary processes and depositional environment. In most of the western part of the Appalachian basin the organic-matter content of the Devonian shale can be estimated from gamma-ray wire-line logs using the equation: phi 0 = (γ/sub B/ - γ)/1.378A, where phi 0 is the organic-matter content of the shale (fractional volume), γ the gamma-ray intensity (API units), γ/sub B/ the gamma-ray intensity if no organic matter is present (API units), and A the slope of the crossplot of gamma-ray intensity and formation density (API units/(g/cm 3 )). Organic-matter contents estimated using this equation are compared with organic-matter contents determined from direct laboratory analyses of organic carbon for 74 intervals of varying thickness from 12 widely separated wells. The organic-matter content of these intervals ranges from near zero to about 20% by volume. The gamma-ray intensity of the Cleveland Member of the Ohio Shale and the lower part of the Olentangy Shale is anomalously low compared to other Devonian shales of similar richness, so that organic-matter content computed for each of these units from gamma-ray logs is likely to be too low. Wire-line methods for estimating organic-matter content have the advantages of economy, readily available sources of data, and continuous sampling of the vertically heterogenous shale section. The gamma-ray log, in particular, is commonly run in the Devonian shale, its response characteristics are well known, and the cumulative pool of gamma-ray logs forms a large and geographically broad data base. The quantitative computation of organic-matter content from gamma-ray logs should be of practical value in studies of the Appalachian Devonian shale. 16 figures

Organic matter processing by microbial communities throughout the Atlantic water column as revealed by metaproteomics

DEFF Research Database (Denmark)

Bergauer, Kristin; Fernandez-Guerra, Antonio; Garcia, Juan A L

2018-01-01

The phylogenetic composition of the heterotrophic microbial community is depth stratified in the oceanic water column down to abyssopelagic layers. In the layers below the euphotic zone, it has been suggested that heterotrophic microbes rely largely on solubilized particulate organic matter...... as a carbon and energy source rather than on dissolved organic matter. To decipher whether changes in the phylogenetic composition with depth are reflected in changes in the bacterial and archaeal transporter proteins, we generated an extensive metaproteomic and metagenomic dataset of microbial communities...... collected from 100- to 5,000-m depth in the Atlantic Ocean. By identifying which compounds of the organic matter pool are absorbed, transported, and incorporated into microbial cells, intriguing insights into organic matter transformation in the deep ocean emerged. On average, solute transporters accounted...

Novel estimation of the humification degree of soil organic matter by laser-induced breakdown spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Ferreira, Edilene Cristina, E-mail: edilene@iq.unesp.br [Embrapa Instrumentation, Rua XV de Novembro, 1452, CEP 13560-970 São Carlos, SP (Brazil); São Paulo State University—UNESP, Analytical Chemistry Department, P.O. Box 355, 14801-970 Rua Prof. Francisco Degni, 55, CEP 14800-900 Araraquara, SP (Brazil); Ferreira, Ednaldo José, E-mail: ednaldo.ferreira@embrapa.br [Embrapa Instrumentation, Rua XV de Novembro, 1452, CEP 13560-970 São Carlos, SP (Brazil); Villas-Boas, Paulino Ribeiro, E-mail: paulino.villas-boas@embrapa.br [Embrapa Instrumentation, Rua XV de Novembro, 1452, CEP 13560-970 São Carlos, SP (Brazil); Senesi, Giorgio Saverio, E-mail: giorgio.senesi@ba.imip.cnr.it [Institute of Inorganic Methodologies and Plasmas, CNR, Bari 70126 (Italy); Carvalho, Camila Miranda, E-mail: camilamc@gmail.com [Embrapa Instrumentation, Rua XV de Novembro, 1452, CEP 13560-970 São Carlos, SP (Brazil); Physics Institute of São Carlos, University of São Paulo, IFSC-USP, Av. Trabalhador são-carlense, 400 Pq. Arnold Schimid, 13566-590 São Carlos, SP (Brazil); Romano, Renan Arnon, E-mail: renan.romano@gmail.com [Embrapa Instrumentation, Rua XV de Novembro, 1452, CEP 13560-970 São Carlos, SP (Brazil); Physics Institute of São Carlos, University of São Paulo, IFSC-USP, Av. Trabalhador são-carlense, 400 Pq. Arnold Schimid, 13566-590 São Carlos, SP (Brazil); Martin-Neto, Ladislau, E-mail: ladislau.martin@embrapa.br [Embrapa Instrumentation, Rua XV de Novembro, 1452, CEP 13560-970 São Carlos, SP (Brazil); and others

2014-09-01

Soil organic matter (SOM) constitutes an important reservoir of terrestrial carbon and can be considered an alternative for atmospheric carbon storage, contributing to global warming mitigation. Soil management can favor atmospheric carbon incorporation into SOM or its release from SOM to atmosphere. Thus, the evaluation of the humification degree (HD), which is an indication of the recalcitrance of SOM, can provide an estimation of the capacity of carbon sequestration by soils under various managements. The HD of SOM can be estimated by using various analytical techniques including fluorescence spectroscopy. In the present work, the potential of laser-induced breakdown spectroscopy (LIBS) to estimate the HD of SOM was evaluated for the first time. Intensities of emission lines of Al, Mg and Ca from LIBS spectra showing correlation with fluorescence emissions determined by laser-induced fluorescence spectroscopy (LIFS) reference technique were used to obtain a multivaried calibration model based on the k-nearest neighbor (k-NN) method. The values predicted by the proposed model (A-LIBS) showed strong correlation with LIFS results with a Pearson's coefficient of 0.87. The HD of SOM obtained after normalizing A-LIBS by total carbon in the sample showed a strong correlation to that determined by LIFS (0.94), thus suggesting the great potential of LIBS for this novel application. - Highlights: • Humification degree of soil organic matter (HD) • Importance of soil organic matter HD in keeping carbon in soil • Laser induced fluorescence spectroscopy (LIFS) for HD estimation (reference method) • New LIBS application to predict HD.

MOTOR 2.0: module for transformation of organic matter and nutrients in soil; user guide and technical documentation

NARCIS (Netherlands)

Assinck, F.B.T.; Rappoldt, C.

2004-01-01

MOTOR is a MOdule describing the Transformation of Organic matteR and nutrients in soil. It calculates the transformations between pools of organic matter and mineral nitrogen in soil. Pools are characterized by a carbon and nitrogen content and can be labelled. MOTOR is a flexible tool because the

Modification of SWAT model for simulation of organic matter in Korean watersheds.

Science.gov (United States)

Jang, Jae-Ho; Jung, Kwang-Wook; Gyeong Yoon, Chun

2012-01-01

The focus of water quality modeling of Korean streams needs to be shifted from dissolved oxygen to algae or organic matter. In particular, the structure of water quality models should be modified to simulate the biochemical oxygen demand (BOD), which is a key factor in calculating total maximum daily loads (TMDLs) in Korea, using 5-day BOD determined in the laboratory (Bottle BOD(5)). Considering the limitations in simulating organic matter under domestic conditions, we attempted to model total organic carbon (TOC) as well as BOD by using a watershed model. For this purpose, the Soil and Water Assessment Tool (SWAT) model was modified and extended to achieve better correspondence between the measured and simulated BOD and TOC concentrations. For simulated BOD in the period 2004-2008, the Nash-Sutcliffe model efficiency coefficient increased from a value of -2.54 to 0.61. Another indicator of organic matter, namely, the simulated TOC concentration showed that the modified SWAT adequately reflected the observed values. The improved model can be used to predict organic matter and hence, may be a potential decision-making tool for TMDLs. However, it needs further testing for longer simulation periods and other catchments.

Spatial sedimentary distribution, seasonality and the characteristics of organic matter on Fernando de Noronha insular shelf

Directory of Open Access Journals (Sweden)

Roberto Lima Barcellos

Full Text Available Abstract The present study was conducted in the Fernando de Noronha archipelago (4°S/32°W. The objective is the evaluation of the spatial distribution and seasonal variations in the sediments and sedimentary organic matter in the northern insular shelf of Fernando de Noronha ("Mar de Dentro". Nineteen surface sediment samples were collected between December 2013, July 2014 and November 2014. The studied methods included analysis of the grain size, coarse fraction, morphoscopy, total organic matter content, calcium carbonate, organic carbon, total nitrogen, sedimentary phosphorus (organic, inorganic and total, elemental ratios (C/N, C/P and stable isotopic ratios (δ13C-δ15N. The results allowed to infer that there is no seasonal variation in sediment distribution. Whereas, the shelf sediments present a calcareous sandy sedimentary cover (CaCO3≈ 88.3%, predominantly of well-sorted fine sands, with low organic matter content (TOM3.0%; TN>0.4% of mixed origin (δ13C= -24.5 to -23.0%PDB, which were related to anthropogenic impacts and the biotic and abiotic local processes.

Persistence of soil organic matter as an ecosystem property

Energy Technology Data Exchange (ETDEWEB)

Schmidt, M.W.; Torn, M. S.; Abiven, S.; Dittmar, T.; Guggenberger, G.; Janssens, I.A.; Kleber, M.; Kögel-Knabner, I.; Lehmann, J.; Manning, D.A.C.; Nannipieri, P.; Rasse, D.P.; Weiner, S.; Trumbore, S.E.

2011-08-15

Globally, soil organic matter (SOM) contains more than three times as much carbon as either the atmosphere or terrestrial vegetation. Yet it remains largely unknown why some SOM persists for millennia whereas other SOM decomposes readily—and this limits our ability to predict how soils will respond to climate change. Recent analytical and experimental advances have demonstrated that molecular structure alone does not control SOM stability: in fact, environmental and biological controls predominate. Here we propose ways to include this understanding in a new generation of experiments and soil carbon models, thereby improving predictions of the SOM response to global warming.

Fungal decomposition of terrestrial organic matter accelerated Early Jurassic climate warming

Science.gov (United States)

Pieńkowski, Grzegorz; Hodbod, Marta; Ullmann, Clemens V.

2016-08-01

Soils - constituting the largest terrestrial carbon pool - are vulnerable to climatic warming. Currently existing uncertainties regarding carbon fluxes within terrestrial systems can be addressed by studies of past carbon cycle dynamics and related climate change recorded in sedimentary successions. Here we show an example from the Early Jurassic (early Toarcian, c. 183 mya) marginal-marine strata from Poland, tracking the hinterland response to climatic changes through a super-greenhouse event. In contrast to anoxia-related enhanced carbon storage in coeval open marine environments, Total Organic Carbon (TOC) concentrations in the Polish successions are substantially reduced during this event. Increasing temperature favoured fungal-mediated decomposition of plant litter - specifically of normally resistant woody tissues. The associated injection of oxidized organic matter into the atmosphere corresponds to abrupt changes in standing vegetation and may have contributed significantly to the amplified greenhouse climate on Earth. The characteristic Toarcian signature of multiple warm pulses coinciding with rapidly decreasing carbon isotope ratios may in part be the result of a radical reduction of the terrestrial carbon pool as a response to climate change.

Quantification of the carbonaceous matter origin in submicron marine aerosol particles by dual carbon isotope analysis

Science.gov (United States)

Ceburnis, D.; Garbaras, A.; Szidat, S.; Rinaldi, M.; Fahrni, S.; Perron, N.; Wacker, L.; Leinert, S.; Remeikis, V.; Facchini, M. C.; Prevot, A. S. H.; Jennings, S. G.; O'Dowd, C. D.

2011-01-01

Dual carbon isotope analysis has been performed for the first time demonstrating a potential in organic matter apportionment between three principal sources: marine, terrestrial (non-fossil) and fossil fuel due to unique isotopic signatures. The results presented here, utilising combinations of dual carbon isotope analysis, provides a conclusive evidence of a dominant biogenic organic fraction to organic aerosol over biologically active oceans. In particular, the NE Atlantic, which is also subjected to notable anthropogenic influences via pollution transport processes, was found to contain 80% organic aerosol matter of biogenic origin directly linked to plankton emissions. The remaining carbonaceous aerosol was of fossil-fuel origin. By contrast, for polluted air advecting out from Europe into the NE Atlantic, the source apportionment is 30% marine biogenic, 40% fossil fuel, and 30% continental non-fossil fuel. The dominant marine organic aerosol source in the atmosphere has significant implications for climate change feedback processes.

Dynamics of dissolved organic carbon in a stream during a quarter century of forest succession

Science.gov (United States)

Judy L. Meyer; Jackson Webster; Jennifer Knoepp; E.F. Benfield

2014-01-01

Dissolved organic carbon (DOC) is a heterogeneous mixture of compounds that makes up a large fraction of the organic matter transported in streams. It plays a significant role in many ecosystems. Riverine DOC links organic carbon cycles of continental and oceanic ecosystems. It is a significant trophic resource in stream food webs. DOC imparts color to lakes,...

Organic matter loading affects lodgepole pine seedling growth.

Science.gov (United States)

Wei, Xiaohua; Li, Qinglin; Waterhouse, M J; Armleder, H M

2012-06-01

Organic matter plays important roles in returning nutrients to the soil, maintaining forest productivity and creating habitats in forest ecosystems. Forest biomass is in increasing demand for energy production, and organic matter has been considered as a potential supply. Thus, an important management question is how much organic matter should be retained after forest harvesting to maintain forest productivity. To address this question, an experimental trial was established in 1996 to evaluate the responses of lodgepole pine seedling growth to organic matter loading treatments. Four organic matter loading treatments were randomly assigned to each of four homogeneous pine sites: removal of all organic matter on the forest floor, organic matter loading quantity similar to whole-tree-harvesting residuals left on site, organic matter loading quantity similar to stem-only-harvesting residuals, and organic matter loading quantity more similar to what would be found in disease- or insect-killed stands. Our 10-year data showed that height and diameter had 29 and 35 % increase, respectively, comparing the treatment with the most organic matter loading to the treatment with the least organic matter loading. The positive response of seedling growth to organic matter loading may be associated with nutrients and/or microclimate change caused by organic matter, and requires further study. The dynamic response of seedling growth to organic matter loading treatments highlights the importance of long-term studies. Implications of those results on organic matter management are discussed in the context of forest productivity sustainability.

Interactions of diuron with dissolved organic matter from organic amendments.

Science.gov (United States)

Thevenot, Mathieu; Dousset, Sylvie; Hertkorn, Norbert; Schmitt-Kopplin, Philippe; Andreux, Francis

2009-07-01

Diuron is frequently detected in some drinking water reservoirs under the Burgundy vineyards, where organic amendments are applied. The environmental effect of these amendments on pesticide transport is ambiguous: on the one hand it could enhance their retention by increasing soil organic carbon content; on the other hand, dissolved organic matter (DOM) could facilitate their transport. Elutions were performed using columns packed with glass beads in order to investigate DOM-diuron interactions, and the possible co-transport of diuron and DOM. Four organic amendments (A, B, C and D) were tested; C and D were sampled at fresh (F) and mature (M) stages. An increase in diuron leaching was observed only for A and D(F) amendments (up to 16% compared to the DOM-free blank samples), suggesting a DOM effect on diuron transport. These results could be explained by the higher DOM leaching for A and D(F) compared to B, C(F), C(M) and D(M) increasing diuron-DOM interactions. These interactions seem to be related to the aromatic and aliphatic content of the DOM, determining formation of hydrogen and non-covalent bonds. The degree of organic matter maturity does not seem to have any effect with amendment C, while a reduction in diuron leaching is observed between D(F) and D(M). After equilibrium dialysis measurement of diuron-DOM complexes, it appeared that less than 3% of the diuron applied corresponded to complexes with a molecular weight >1000 Da. Complexes <1000 Da could also take part in this facilitated transport.

Spectroscopic study of the water-soluble organic matter isolated from atmospheric aerosols collected under different atmospheric conditions

International Nuclear Information System (INIS)

Duarte, Regina M.B.O.; Pio, Casimiro A.; Duarte, Armando C.

2005-01-01

The composition of the water-soluble organic matter from fine aerosols collected in a rural location during two different meteorological conditions (summer and autumn) was investigated by UV-vis, synchronous fluorescence (with Δλ = 20 nm), FT-IR and CPMAS- 13 C NMR spectroscopies. A seasonal variation in the concentration of total carbon, organic carbon and water-soluble organic carbon was confirmed, with higher values during the autumn and lower values during the summer season. The chemical characterisation of the water-soluble organic matter showed that both samples are dominated by a high content of aliphatic structures, carboxyl groups and aliphatic carbons single bonded to one oxygen or nitrogen atom. However, the autumn sample exhibits a higher aromatic content than the summer sample, plus signals due to carbons of phenol, ketones and methoxyl groups. These signals were attributed to lignin breakdown products which are likely to be released during wood combustion processes. The obtained results put into evidence the major contribution of biomass burning processes in domestic fireplaces during low temperature conditions into both the concentration and the bulk chemical properties of the WSOC from fine aerosols

Microbial respiration, but not biomass, responded linearly to increasing light fraction organic matter input: Consequences for carbon sequestration.

Science.gov (United States)

Rui, Yichao; Murphy, Daniel V; Wang, Xiaoli; Hoyle, Frances C

2016-10-18

Rebuilding 'lost' soil carbon (C) is a priority in mitigating climate change and underpinning key soil functions that support ecosystem services. Microorganisms determine if fresh C input is converted into stable soil organic matter (SOM) or lost as CO 2 . Here we quantified if microbial biomass and respiration responded positively to addition of light fraction organic matter (LFOM, representing recent inputs of plant residue) in an infertile semi-arid agricultural soil. Field trial soil with different historical plant residue inputs [soil C content: control (tilled) = 9.6 t C ha -1 versus tilled + plant residue treatment (tilled + OM) = 18.0 t C ha -1 ] were incubated in the laboratory with a gradient of LFOM equivalent to 0 to 3.8 t C ha -1 (0 to 500% LFOM). Microbial biomass C significantly declined under increased rates of LFOM addition while microbial respiration increased linearly, leading to a decrease in the microbial C use efficiency. We hypothesise this was due to insufficient nutrients to form new microbial biomass as LFOM input increased the ratio of C to nitrogen, phosphorus and sulphur of soil. Increased CO 2 efflux but constrained microbial growth in response to LFOM input demonstrated the difficulty for C storage in this environment.

Quantifying immediate radiative forcing by black carbon and organic matter with the Specific Forcing Pulse

Directory of Open Access Journals (Sweden)

T. C. Bond

2011-02-01

Full Text Available Climatic effects of short-lived climate forcers (SLCFs differ from those of long-lived greenhouse gases, because they occur rapidly after emission and because they depend upon the region of emission. The distinctive temporal and spatial nature of these impacts is not captured by measures that rely on global averages or long time integrations. Here, we propose a simple measure, the Specific Forcing Pulse (SFP, to quantify climate warming or cooling by these pollutants, where we define "immediate" as occurring primarily within the first year after emission. SFP is the amount of energy added to or removed from a receptor region in the Earth-atmosphere system by a chemical species, per mass of emission in a source region. We limit the application of SFP to species that remain in the atmosphere for less than one year. Metrics used in policy discussions, such as total forcing or global warming potential, are easily derived from SFP. However, SFP conveys purely physical information without incurring the policy implications of choosing a time horizon for the global warming potential.

Using one model (Community Atmosphere Model, or CAM, we calculate values of SFP for black carbon (BC and organic matter (OM emitted from 23 source-region combinations. Global SFP for both atmosphere and cryosphere impacts is divided among receptor latitudes. SFP is usually greater for open-burning emissions than for energy-related (fossil-fuel and biofuel emissions because of the timing of emission. Global SFP for BC varies by about 45% for energy-related emissions from different regions. This variation would be larger except for compensating effects. When emitted aerosol has larger cryosphere forcing, it often has lower atmosphere forcing because of less deep convection and a shorter atmospheric lifetime.

A single model result is insufficient to capture uncertainty. We develop a best estimate and uncertainties for SFP by combining forcing results from

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

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

Science.gov (United States)

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

2006-01-01

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

Mycorrhizal associations of trees have different indirect effects on organic matter decomposition

Science.gov (United States)

Melanie K. Taylor; Richard A. Lankau; Nina Wurzburger; Franciska de Vries

2016-01-01

1. Organic matter decomposition is the main process by which carbon (C) is lost from terrestrialecosystems, and mycorrhizal associations of plants (i.e. arbuscular mycorrhizas (AM) and ectomycorrhizas(ECM)) may have different indirect effects on this loss pathway. AM and ECM plants differin the soil...

Effects of organic matter removal and soil compaction on fifth-year mineral soil carbon and nitrogen contents for sites across the United States and Canada

Science.gov (United States)

Felipe G. Sanchez; Allan E. Tiarks; J. Marty Kranabetter; Deborah S. Page-Dumroese; Robert F. Powers; Paul T. Sanborn; William K. Chapman

2006-01-01

This study describes the main treatment effects of organic matter removal and compaction and a split-plot effect of competition control on mineral soil carbon (C) and nitrogen (N) pools. Treatment effects on soil C and N pools are discussed for 19 sites across five locations (British Columbia, Northern Rocky Mountains, Pacific Southwest, and Atlantic and Gulf coasts)...

Ligand extraction of rare earth elements from aquifer sediments: Implications for rare earth element complexation with organic matter in natural waters

Science.gov (United States)

Tang, Jianwu; Johannesson, Karen H.

2010-12-01

The ability of organic matter as well as carbonate ions to extract rare earth elements (REEs) from sandy sediments of a Coastal Plain aquifer was investigated for unpurified organic matter from different sources (i.e., Mississippi River natural organic matter, Aldrich humic acid, Nordic aquatic fulvic acid, Suwannee River fulvic acid, and Suwannee River natural organic matter) and for extraction solutions containing weak (i.e., CH 3COO -) or strong (i.e., CO32-) ligands. The experimental results indicate that, in the absence of strong REE complexing ligands in solution, the amount of REEs released from the sand is small and the fractionation pattern of the released REEs appears to be controlled by the surface stability constants for REE sorption with Fe(III) oxides/oxyhydroxides. In the presence of strong solution complexing ligands, however, the amount and the fractionation pattern of the released REEs reflect the strength and variation of the stability constants of the dominant aqueous REE species across the REE series. The varying amount of REEs extracted by the different organic matter employed in the experiments indicates that organic matter from different sources has different complexing capacity for REEs. However, the fractionation pattern of REEs extracted by the various organic matter used in our experiments is remarkable consistent, being independent of the source and the concentration of organic matter used, as well as solution pH. Because natural aquifer sand and unpurified organic matter were used in our experiments, our experimental conditions are more broadly similar to natural systems than many previous laboratory experiments of REE-humic complexation that employed purified humic substances. Our results suggest that the REE loading effect on REE-humic complexation is negligible in natural waters as more abundant metal cations (e.g., Fe, Al) out-compete REEs for strong binding sites on organic matter. More specifically, our results indicate that REE

Chromophoric Dissolved Organic Matter in Southwestern Greenland Lakes

Science.gov (United States)

Osburn, C. L.; Giles, M. E.; Underwood, G. J. C.

2014-12-01

Dissolved organic matter (DOM) is an important property of Arctic lake ecosystems, originating from allochthonous inputs from catchments and autochthonous production by plankton in the water column. Little is known about the quality of DOM in Arctic lakes that lack substantial inputs from catchments and such lakes are abundant in southwestern Greenland. Colored dissolved organic matter (CDOM), the fraction that absorbs ultraviolet (UV) and visible light, is the controlling factor for the optical properties of many surface waters and as well informs on the quality of DOM. We examined the quality of CDOM in 21 lakes in southwestern Greenland, from the ice sheet to the coast, as part of a larger study examining the role of DOM in regulating microbial communities in these lakes. DOM was size fractioned and absorbance and fluorescence was measured on each size fraction, as well as on bulk DOM. The specific ultraviolet absorbance (SUVA) at 254 nm (SUVA254), computed by normalizing absorption (a254) to dissolved organic carbon (DOC) concentration, provided an estimate of the aromatic carbon content of DOM. SUVA values were generally CDOM fluorescence was used to determine the relative abundance of allochthonous and autochthonous DOM in all size fractions. Younger lakes near the ice sheet and lakes near the coast had lower amounts of CDOM and appeared more microbial in quality. However, lakes centrally located between the ice sheet and the coast had the highest CDOM concentrations and exhibited strong humic fluorescence. Overall distinct differences in CDOM quality were observed between lake locations and among DOM size fractions.

Tracing the long-term microbial production of recalcitrant fluorescent dissolved organic matter in seawater

DEFF Research Database (Denmark)

Jørgensen, Linda; Stedmon, Colin A.; Granskog, Mats A.

2014-01-01

The majority of dissolved organic matter (DOM) in the ocean is resistant to microbial degradation, yet its formation remains poorly understood. The fluorescent fraction of DOM can be used to trace the formation of recalcitrant DOM (RDOM). A long-term (> 1 year) experiment revealed 27–52% removal...... of dissolved organic carbon and a nonlinear increase in RDOM fluorescence associated with microbial turnover of semilabile DOM. This fluorescence was also produced using glucose as the only initial carbon source, suggesting that degradation of prokaryote remnants contributes to RDOM. Our results indicate...... that the formation of a fluorescent RDOM component depends on the bioavailability of the substrate: the less labile, the larger the production of fluorescent RDOM relative to organic carbon remineralized. The anticipated increase in microbial carbon demand due to ocean warming can potentially forcemicrobes...

Effects of effluent organic matter characteristics on the removal of bulk organic matter and selected pharmaceutically active compounds during managed aquifer recharge: Column study

Science.gov (United States)

Maeng, Sung Kyu; Sharma, Saroj K.; Abel, Chol D. T.; Magic-Knezev, Aleksandra; Song, Kyung-Guen; Amy, Gary L.

2012-10-01

Soil column experiments were conducted to investigate the effects of effluent organic matter (EfOM) characteristics on the removal of bulk organic matter (OM) and pharmaceutically active compounds (PhACs) during managed aquifer recharge (MAR) treatment processes. The fate of bulk OM and PhACs during an MAR is important to assess post-treatment requirements. Biodegradable OM from EfOM, originating from biological wastewater treatment, was effectively removed during soil passage. Based on a fluorescence excitation-emission matrix (F-EEM) analysis of wastewater effluent-dominated (WWE-dom) surface water (SW), protein-like substances, i.e., biopolymers, were removed more favorably than fluorescent humic-like substances under oxic compared to anoxic conditions. However, there was no preferential removal of biopolymers or humic substances, determined as dissolved organic carbon (DOC) observed via liquid chromatography with online organic carbon detection (LC-OCD) analysis. Most of the selected PhACs exhibited removal efficiencies of greater than 90% in both SW and WWE-dom SW. However, the removal efficiencies of bezafibrate, diclofenac and gemfibrozil were relatively low in WWE-dom SW, which contained more biodegradable OM than did SW (copiotrophic metabolism). Based on this study, low biodegradable fractions such as humic substances in MR may have enhanced the degradation of diclofenac, gemfibrozil and bezafibrate by inducing an oligotrophic microbial community via long term starvation. Both carbamazepine and clofibric acid showed persistent behaviors and were not influenced by EfOM.

Effects of effluent organic matter characteristics on the removal of bulk organic matter and selected pharmaceutically active compounds during managed aquifer recharge: Column study

KAUST Repository

Maeng, Sungkyu

2012-10-01

Soil column experiments were conducted to investigate the effects of effluent organic matter (EfOM) characteristics on the removal of bulk organic matter (OM) and pharmaceutically active compounds (PhACs) during managed aquifer recharge (MAR) treatment processes. The fate of bulk OM and PhACs during an MAR is important to assess post-treatment requirements. Biodegradable OM from EfOM, originating from biological wastewater treatment, was effectively removed during soil passage. Based on a fluorescence excitation-emission matrix (F-EEM) analysis of wastewater effluent-dominated (WWE-dom) surface water (SW), protein-like substances, i.e., biopolymers, were removed more favorably than fluorescent humic-like substances under oxic compared to anoxic conditions. However, there was no preferential removal of biopolymers or humic substances, determined as dissolved organic carbon (DOC) observed via liquid chromatography with online organic carbon detection (LC-OCD) analysis. Most of the selected PhACs exhibited removal efficiencies of greater than 90% in both SW and WWE-dom SW. However, the removal efficiencies of bezafibrate, diclofenac and gemfibrozil were relatively low in WWE-dom SW, which contained more biodegradable OM than did SW (copiotrophic metabolism). Based on this study, low biodegradable fractions such as humic substances in MR may have enhanced the degradation of diclofenac, gemfibrozil and bezafibrate by inducing an oligotrophic microbial community via long term starvation. Both carbamazepine and clofibric acid showed persistent behaviors and were not influenced by EfOM. © 2012 Elsevier B.V.

Effects of effluent organic matter characteristics on the removal of bulk organic matter and selected pharmaceutically active compounds during managed aquifer recharge: Column study.

Science.gov (United States)

Maeng, Sung Kyu; Sharma, Saroj K; Abel, Chol D T; Magic-Knezev, Aleksandra; Song, Kyung-Guen; Amy, Gary L

2012-10-01

Soil column experiments were conducted to investigate the effects of effluent organic matter (EfOM) characteristics on the removal of bulk organic matter (OM) and pharmaceutically active compounds (PhACs) during managed aquifer recharge (MAR) treatment processes. The fate of bulk OM and PhACs during an MAR is important to assess post-treatment requirements. Biodegradable OM from EfOM, originating from biological wastewater treatment, was effectively removed during soil passage. Based on a fluorescence excitation-emission matrix (F-EEM) analysis of wastewater effluent-dominated (WWE-dom) surface water (SW), protein-like substances, i.e., biopolymers, were removed more favorably than fluorescent humic-like substances under oxic compared to anoxic conditions. However, there was no preferential removal of biopolymers or humic substances, determined as dissolved organic carbon (DOC) observed via liquid chromatography with online organic carbon detection (LC-OCD) analysis. Most of the selected PhACs exhibited removal efficiencies of greater than 90% in both SW and WWE-dom SW. However, the removal efficiencies of bezafibrate, diclofenac and gemfibrozil were relatively low in WWE-dom SW, which contained more biodegradable OM than did SW (copiotrophic metabolism). Based on this study, low biodegradable fractions such as humic substances in MR may have enhanced the degradation of diclofenac, gemfibrozil and bezafibrate by inducing an oligotrophic microbial community via long term starvation. Both carbamazepine and clofibric acid showed persistent behaviors and were not influenced by EfOM. Copyright © 2012 Elsevier B.V. All rights reserved.

Black Carbon, Dust and Organic Matter at South Cascade Glacier in Washington State, USA: A Comprehensive Characterization of Temporal (1865-2014) and Spatial Variability

Science.gov (United States)

Kaspari, S.; Pittenger, D.; Swick, M.; Skiles, M.; Perez, A.; Sethi, H.; Sevier, E.

2017-12-01

Rising temperatures are a widely recognized cause of glacial retreat in Washington, however light absorbing aerosols (LAA, including black carbon (BC), dust and organic matter) can also contribute to increased melt by reducing snow albedo. We present updated results of BC and dust variability at South Cascade (SOCAS) glacier spanning 1865-1994 using a 158 m ice core. Peak BC deposition occurred between 1940-1958, when median BC concentrations were 25 times higher than background levels. Post 1958 BC concentrations decrease, followed by an increase post 1980 associated with melt consolidation and/or trans-Pacific aerosol transport. Dust deposition at SOCAS is dominated by local sources. Albedo reductions from LAA are dominated by dust deposition, except during high BC deposition events from wildfires, and during the 1940-1958 period when BC contributes equally to albedo reductions. Results from a 2014 field campaign that included collection of 3 shallow ice cores, surface snow, and snow albedo measurements allow the 1865-1994 ice core record to be extended toward present, and spatial variability in LAA to be characterized. Snow albedo transects were measured using a spectrometer. BC concentrations were measured using a Single Particle Soot Photometer (SP2). Gravimetric filtration was used to determine the total LAA, and a thermal gravimetric technique was used to partition the LAA between dust and organic matter. The organic matter was partitioned into organic and elemental carbon using a thermal optical method. These methods allow LAA abundances be measured, but to partition the contribution of the LAA to albedo reductions requires characterization of LAA optical properties. This was accomplished using a Hyperspectral Imaging Microscope Spectrometer method that allows particle reflectance to be measured at 138 nm2 pixel resolution. By combining these methods, we provide a comprehensive characterization of spatial and temporal LAA variability at SOCAS.

Iron traps terrestrially derived dissolved organic matter at redox interfaces

Science.gov (United States)

Riedel, Thomas; Zak, Dominik; Biester, Harald; Dittmar, Thorsten

2013-01-01

Reactive iron and organic carbon are intimately associated in soils and sediments. However, to date, the organic compounds involved are uncharacterized on the molecular level. At redox interfaces in peatlands, where the biogeochemical cycles of iron and dissolved organic matter (DOM) are coupled, this issue can readily be studied. We found that precipitation of iron hydroxides at the oxic surface layer of two rewetted fens removed a large fraction of DOM via coagulation. On aeration of anoxic fen pore waters, >90% of dissolved iron and 27 ± 7% (mean ± SD) of dissolved organic carbon were rapidly (within 24 h) removed. Using ultra-high-resolution MS, we show that vascular plant-derived aromatic and pyrogenic compounds were preferentially retained, whereas the majority of carboxyl-rich aliphatic acids remained in solution. We propose that redox interfaces, which are ubiquitous in marine and terrestrial settings, are selective yet intermediate barriers that limit the flux of land-derived DOM to oceanic waters. PMID:23733946

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.

Hydrogen and carbon isotopes of petroleum and related organic matter

International Nuclear Information System (INIS)

Yeh, H.W.; Epstein, S.

1981-01-01

D/H and 13 C/ 12 C ratios were measured for 114 petroleum samples and for several samples of related organic matter. DeltaD of crude oil ranges from -85 to -181 per thousand except for one distillate (-250 per thousand) from the Kenai gas field; delta 13 C of crude oil ranges from -23.3 to -32.5 per thousand. Variation in deltaD and delta 13 C values of compound-grouped fractions of a crude oil is small, 3 and 1.1 per thousand, respectively, and the difference in deltaD and delta 13 C between oil and coeval wax is slight. Gas fractions are 53 to 70 and 22.6 to 23.2 per thousand depleted in D and 13 C, respectively, relative to the coexisting oil fractions. The deltaD and delta 13 C values of the crude oils appear to be largely determined by the isotopic compositions of their organic precursors. The contribution of terrestrial organic debris to the organic precursors of most marine crude oils may be significant. (author)

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

Agriculture Organic Matter and Chicken Manure

Directory of Open Access Journals (Sweden)

Süleyman Taban

2013-11-01

Full Text Available Undo ubtedly organic matter content of soils is one of theim portant factor for high quality and abundant crop production. In addition to improve the physical properties ofsoil, organic matter contributest ocrop production viabeing energy source formicro-organisms in soiland contained plantnutrients. Fiftypercent of theagri cultures oil contains 1-2 % organicmatter in Turkey.In addition to being a sourceof organic matter, organic poultry manurefertilizer isricherthan other organic fertilizerse specially nitrogen content. It is possible to eliminate poultry manure based salt stress and disease factors with composting process in proper conditions.

Biochemical and stable carbon isotope records of mangrove derived organic matter in the sediment cores

Digital Repository Service at National Institute of Oceanography (India)

Manju, M.N.; Resmi, P.; RatheeshKumar, C.S.; Gireeshkumar, T.R.; Chandramohanakumar, N.; Joseph, M.M.

in mangrove sediments. This also confirms the involvement of heterotrophic microorganisms in the organic carbon dynamics of the study area. The bulk elemental ratio (total organic carbon/total nitrogen) varied between 11.39 and 24.14 in the study region...

Organic carbon and nitrogen stable isotopes in the intertidal sediments from the Yangtze Estuary, China

International Nuclear Information System (INIS)

Liu, M. . E-mail mliu@geo.ecnu.edu.cn; Hou, L.J.; Xu, S.Y.; Ou, D.N.; Yang, Y.; Yu, J.; Wang, Q.

2006-01-01

The natural isotopic compositions and C/N elemental ratios of sedimentary organic matter were determined in the intertidal flat of the Yangtze Estuary. The results showed that the ratios of carbon and nitrogen stable isotopes were respectively -29.8 per mille to - 26.0 per mille and 1.6 per mille -5.5 per mille in the flood season (July), while they were -27.3 per mille to - 25.6 per mille and 1.7 per mille -7.8 per mille in the dry season (February), respectively. The δ 13 C signatures were remarkably higher in July than in February, and gradually increased from the freshwater areas to the brackish areas. In contrast, there were relatively complex seasonal and spatial changes in stable nitrogen isotopes. It was also reflected that δ 15 N and C/N compositions had been obviously modified by organic matter diagenesis and biological processing, and could not be used to trace the sources of organic matter at the study area. In addition, it was considered that the mixing inputs of terrigenous and marine materials generally dominated sedimentary organic matter in the intertidal flat. The contribution of terrigenous inputs to sedimentary organic matter was roughly estimated according to the mixing balance model of stable carbon isotopes

Archaeal remains dominate marine organic matter from the early Albian oceanic anoxic event 1b

DEFF Research Database (Denmark)

Kuypers, M.M.M.; Blokker, P.; Hopmans, E.C.

2002-01-01

The sources for both soluble and insoluble organic matter of the early Albian (∼112 Myr) oceanic anoxic event (OAE) 1b black shales of the Ocean Drilling Program (ODP) site 1049C (North Atlantic Ocean off the coast of Florida) and the Ravel section of the Southeast France Basin (SEFB) were...... in C/C ratios was used to estimate that up to ∼40% of the organic matter of the SEFB and up to ∼80% of the organic matter of ODP site 1049C preserved in the black shales is derived from archaea. Furthermore, it is shown that, even though there are apparent similarities (high organic carbon (OC) content......, distinct lamination, C-enrichment of OC) between the black shales of OAE1b and the Cenomanian/Turonian (∼94 Myr) OAE, the origin of the organic matter (archaeal versus phytoplanktonic) and causes for C-enrichment of OC are completely different....

Decomposition of litter and soil organic matter - Can we distinguish a mechanism for soil organic matter buildup ?

International Nuclear Information System (INIS)

Berg, B.; Johansson, M.B.; McClaugherty, C.; Virzo de Santo, A.; Ekbohm, G.

1995-01-01

This synthesis paper presents a model for estimating the buildup of soil organic matter in various types of coniferous forests. The knowledge used was obtained from a well-studied forest with good litterfall data, decomposition information and validation measurements of the soil organic matter layer. By constructing a simple model for litterfall, and the information on maximum decomposition levels for litter, we could estimate the annual increase in soil organic matter and extend this to encompass stand age. The validation measurement and the estimated amount of soil organic matter differed by about 8 or 26% over a 120-yr period, depending on the litterfall model. The estimated increased storage of soil organic matter as a consequence of climate change was found to be drastic. We thus found that the soil organic matter layer would grow about four times as fast as a result of the needle component only. This estimate was based on a comparison between latitudes with a difference of 17 degrees. 35 refs, 7 figs, 3 tabs

Soil organic matter formation and sequestration across a forested floodplain chronosequence

Science.gov (United States)

John D. Wigginton; B. Graeme Lockaby; Carl C. Trettin

2000-01-01

Successional changes in soil organic matter formation and carbon sequestration across a forested floodplain chronosequence were studied at the Savannah river site, National Environmental Research Park, SC, US. Four floodplain sites were selected for study, three of which are in various stages of recovery from impact due to thermal effluent discharge. The fourth is a...

Assessing the Impact of Land Management on Organic Matter Composition in Peat Soils

Science.gov (United States)

Savage, A.; Holden, J.; Wainwright, J.

2010-05-01

Peatlands are seen as important stores of terrestrial carbon, accounting for up to one-third of global soil carbon stocks. In some cases peatlands are shown to be emitters of carbon, in other cases carbon sinks depending on the site conditions and nature of degradation. However, carbon budget calculations carried out to date have a number of uncertainties associated with them and the composition of the carbon is generally not considered when determining carbon budgets. Carbon cycling in peat is driven by four key factors (Laiho, 2006):, environmental conditions (e.g. temperature, water table level), substrate quality (e.g. how recalcitrant the peat is), nutrients (e.g. nitrogen required to synthesis the carbon stocks) and microbial community (e.g. are the microbes present able to utilise the available substrate). Land management is also recognised as an additional driver, but the impacts of many types of management are poorly understood. Among the four drivers listed by Laiho (2006) substrate quality is seen as the most significant. To date, little work has been carried out to characterise the quality of organic matter in peat soils; rather crude estimates have been made as to the quantity of carbon that is stored in peatlands, yet without understanding the composition of the peat, limitations are imposed on calculations of rates of carbon loss from peatlands. This work seeks to examine how variations in the chemical composition of organic matter in peat varies with land use. The method published by Wieder and Starr (1998) was followed to determine eight fractions: soluble fats and waxes, hot water soluble, hollocellulose, cellulose, soluble phenolics, acid insoluble carbohydrates, water soluble carbohydrates and lignin. Samples were taken from burnt, grazed, drained, afforested and undisturbed sites at the Moor House UNESCO Biosphere Reserve in Northern England. The method was used to identify if differences were present in the recalcitrance of the peat and linked

Organic matter turnover in subsoils: current knowledge and future challenges

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Marschner, Bernd

2014-05-01

In the past, carbon flux measurements and modelling have mostly considered the topsoil where C-concentrations, root densities and microbial activities are generally highest. However, depending on climate zone and land use, this soil compartment contains only 30-50% of the C-stocks of the first meter. If the deeper subsoil down to 3 m is also considered, the contribution of topsoil carbon stocks to total soil C-pools is only 20-40%. Another distinct property of subsoil organic matter is its high apparent 14C age. The 14C age of bulk soil organic matter below 30 cm depth generally increases continuously indicating mean residence times of several 103 to 104 years. Large pool size and high radiocarbon age suggest that subsoil OM has accumulated at very low rates over very long time periods and therefore appears to be very stable. In this review, several hypotheses for explaining why subsoil SOM is so seemingly old and inert are presented. These questions are being addressed in a recently granted German research unit consisting of 9 subprojects from all soil science disciplines using field measurements of C-fluxes, 14C analyses and conducting field and lab experiments.

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

Granular activated carbon adsorption of MIB in the presence of dissolved organic matter.

Science.gov (United States)

Summers, R Scott; Kim, Soo Myung; Shimabuku, Kyle; Chae, Seon-Ha; Corwin, Christopher J

2013-06-15

Based on the results of over twenty laboratory granular activated carbon (GAC) column runs, models were developed and utilized for the prediction of 2-methylisoborneol (MIB) breakthrough behavior at parts per trillion levels and verified with pilot-scale data. The influent MIB concentration was found not to impact the concentration normalized breakthrough. Increasing influent background dissolved organic matter (DOM) concentration was found to systematically decrease the GAC adsorption capacity for MIB. A series of empirical models were developed that related the throughput in bed volumes for a range of MIB breakthrough targets to the influent DOM concentration. The proportional diffusivity (PD) designed rapid small-scale column test (RSSCT) could be directly used to scale-up MIB breakthrough performance below 15% breakthrough. The empirical model to predict the throughput to 50% breakthrough based on the influent DOM concentration served as input to the pore diffusion model (PDM) and well-predicted the MIB breakthrough performance below a 50% breakthrough. The PDM predictions of throughput to 10% breakthrough well simulated the PD-RSSCT and pilot-scale 10% MIB breakthrough. Copyright © 2013 Elsevier Ltd. All rights reserved.

Microbial Communities and Organic Matter Composition in Surface and Subsurface Sediments of the Helgoland Mud Area, North Sea

Science.gov (United States)

Oni, Oluwatobi E.; Schmidt, Frauke; Miyatake, Tetsuro; Kasten, Sabine; Witt, Matthias; Hinrichs, Kai-Uwe; Friedrich, Michael W.

2015-01-01

The role of microorganisms in the cycling of sedimentary organic carbon is a crucial one. To better understand relationships between molecular composition of a potentially bioavailable fraction of organic matter and microbial populations, bacterial and archaeal communities were characterized using pyrosequencing-based 16S rRNA gene analysis in surface (top 30 cm) and subsurface/deeper sediments (30–530 cm) of the Helgoland mud area, North Sea. Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (FT-ICR MS) was used to characterize a potentially bioavailable organic matter fraction (hot-water extractable organic matter, WE-OM). Algal polymer-associated microbial populations such as members of the Gammaproteobacteria, Bacteroidetes, and Verrucomicrobia were dominant in surface sediments while members of the Chloroflexi (Dehalococcoidales and candidate order GIF9) and Miscellaneous Crenarchaeota Groups (MCG), both of which are linked to degradation of more recalcitrant, aromatic compounds and detrital proteins, were dominant in subsurface sediments. Microbial populations dominant in subsurface sediments (Chloroflexi, members of MCG, and Thermoplasmata) showed strong correlations to total organic carbon (TOC) content. Changes of WE-OM with sediment depth reveal molecular transformations from oxygen-rich [high oxygen to carbon (O/C), low hydrogen to carbon (H/C) ratios] aromatic compounds and highly unsaturated compounds toward compounds with lower O/C and higher H/C ratios. The observed molecular changes were most pronounced in organic compounds containing only CHO atoms. Our data thus, highlights classes of sedimentary organic compounds that may serve as microbial energy sources in methanic marine subsurface environments. PMID:26635758

Soil organic matter dynamics after the conversion of arable land to pasture

NARCIS (Netherlands)

Römkens, P.F.A.M.; Plicht, van der J.; Hassink, J.

1999-01-01

Conversion of arable land (maize) to pasture will affect the soil organic matter (SOM) content. Changes in the SOM content were studied using a size- and density-fractionation method and 13C analysis. Twenty-six years of maize cropping had resulted in a depletion of carbon stored in the

Quality of fresh organic matter affects priming of soil organic matter and substrate utilization patterns of microbes

Science.gov (United States)

Wang, Hui; Boutton, Thomas W.; Xu, Wenhua; Hu, Guoqing; Jiang, Ping; Bai, Edith

2015-05-01

Changes in biogeochemical cycles and the climate system due to human activities are expected to change the quantity and quality of plant litter inputs to soils. How changing quality of fresh organic matter (FOM) might influence the priming effect (PE) on soil organic matter (SOM) mineralization is still under debate. Here we determined the PE induced by two 13C-labeled FOMs with contrasting nutritional quality (leaf vs. stalk of Zea mays L.). Soils from two different forest types yielded consistent results: soils amended with leaf tissue switched faster from negative PE to positive PE due to greater microbial growth compared to soils amended with stalks. However, after 16 d of incubation, soils amended with stalks had a higher PE than those amended with leaf. Phospholipid fatty acid (PLFA) results suggested that microbial demand for carbon and other nutrients was one of the major determinants of the PE observed. Therefore, consideration of both microbial demands for nutrients and FOM supply simultaneously is essential to understand the underlying mechanisms of PE. Our study provided evidence that changes in FOM quality could affect microbial utilization of substrate and PE on SOM mineralization, which may exacerbate global warming problems under future climate change.

Agricultural practices that store organic carbon in soils: is it only a matter of inputs ?

Science.gov (United States)

Chenu, Claire; Cardinael, Rémi; Autret, Bénédicte; Chevallier, Tiphaine; Girardin, Cyril; Mary, Bruno

2016-04-01

soil organic matter mineralisation rates. This questions our understanding of the stabilization processes of organic matter in soils and especially that of physical protection. The conditions and scale, both spatial and temporal, of physical protection of organic matter are discussed in light of recent literature.

Speciation and Distribution of Trace Metals and Organic Matter in Marine Lake as In Situ Laboratory

Science.gov (United States)

Mlakar, M.; Fiket, Ž.; Cuculić, V.; Cukrov, N.; Geček, S.

2016-02-01

Marine lakes are unique, isolated marine systems, also recognized as in situ "laboratories" in which geochemical processes on a different scale compared to the open sea, can be observed. Impact of organic matter cycling on distribution of trace metals in the marine lake Mir, located on Dugi Otok Island, in the central part of the eastern Adriatic Sea, was investigated. Intense spatial and seasonal variations of physico-chemical parameters and organic matter concentrations in the water column of the Lake are governed predominantly by natural processes. Enhanced oxygen consumption in the Lake during summer season, high organic carbon concentrations and low redox potential result in occasional occurrence of anoxic conditions in the bottom layers. Speciation modelling showed that dissolved trace metals Cu, Pb and Zn, are mostly bound to organic matter, while Cd, Co and Ni are present predominantly as free ions and inorganic complexes. Trace metals removal from the water column and their retention in the sediment was found to depend on the nature of the relationship between specific metal and high proportion of organic matter (up to 9%) and inorganic phases, Fe-oxyhydroxydes or biogenic calcite. Surrounding karstic background, with occasional occurrences of red soil characterize deposited sediments as coarse grained and carbonate rich, whose elemental composition is affected by bathymetry of the basin and overall biological production.

The flux of organic matter through a peatland ecosystem: The role of cellulose, lignin, and their control of the ecosystem oxidation state

Science.gov (United States)

Worrall, Fred; Moody, Catherine S.; Clay, Gareth D.; Burt, Tim P.; Rose, Rob

2017-07-01

This study used thermogravimetric analysis (TGA) to study the transit of organic C through a peatland ecosystem. The biomass, litter, peat soil profile, particulate organic matter (POM), and dissolved organic matter (DOM) fluxes were sampled from the Moor House National Nature Reserve, a peat-covered catchment in northern England where both the dry matter and carbon budget for the catchment were known. The study showed that although TGA traces showed distinct differences between organic matter reservoirs and fluxes, the traces could not readily be associated with particular functionalities or elemental properties. The TGA trace shows that polysaccharides are preferentially removed by humification and degradation with residual peat being dominated by lignin compositions. The DOM is derived from the degradation of lignin while the POM is derived from erosion of the peat profile. The carbon lost as gases (CO2 and CH4) was estimated to be composed of 92 to 95% polysaccharide carbon. The composition of the organic matter lost from the peat ecosystem means that the oxidative ratio (OR) of the ecosystem experienced by the atmosphere was between 0.96 and 0.99: currently, the Intergovernmental Panel on Climate Change uses an OR value of 1.1 for all ecosystems.

Carbon stock and humification index of organic matter affected by sugarcane straw and soil management

Directory of Open Access Journals (Sweden)

Aline Segnini

2013-10-01

Full Text Available The maintenance of sugarcane (Saccharum spp. straw on a soil surface increases the soil carbon (C stocks, but at lower rates than expected. This fact is probably associated with the soil management adopted during sugarcane replanting. This study aimed to assess the impact on soil C stocks and the humification index of soil organic matter (SOM of adopting no-tillage (NT and conventional tillage (CT for sugarcane replanting. A greater C content and stock was observed in the NT area, but only in the 0-5 cm soil layer (p < 0.05. Greater soil C stock (0-60 cm was found in soil under NT, when compared to CT and the baseline. While C stock of 116 Mg ha-1 was found in the baseline area, in areas under CT and NT systems the values ranged from 120 to 127 Mg ha-1. Carbon retention rates of 0.67 and 1.63 Mg C ha-1 year-1 were obtained in areas under CT and NT, respectively. Laser-Induced Fluorescence Spectroscopy showed that CT makes the soil surface (0-20 cm more homogeneous than the NT system due to the effect of soil disturbance, and that the SOM humification index (H LIF is larger in CT compared to NT conditions. In contrast, NT had a gradient of increasing H LIF, showing that the entry of labile organic material such as straw is also responsible for the accumulation of C in this system. The maintenance of straw on the soil surface and the adoption of NT during sugarcane planting are strategies that can increase soil C sequestration in the Brazilian sugarcane sector.

Adsorption of organic contaminants by graphene nanosheets, carbon nanotubes and granular activated carbons under natural organic matter preloading conditions.

Science.gov (United States)

Ersan, Gamze; Kaya, Yasemin; Apul, Onur G; Karanfil, Tanju

2016-09-15

The effect of NOM preloading on the adsorption of phenanthrene (PNT) and trichloroethylene (TCE) by pristine graphene nanosheets (GNS) and graphene oxide nanosheet (GO) was investigated and compared with those of a single-walled carbon nanotube (SWCNT), a multi-walled carbon nanotube (MWCNT), and two coal based granular activated carbons (GACs). PNT uptake was higher than TCE by all adsorbents on both mass and surface area bases. This was attributed to the hydrophobicity of PNT. The adsorption capacities of PNT and TCE depend on the accessibility of the organic molecules to the inner regions of the adsorbent which was influenced from the molecular size of OCs. The adsorption capacities of all adsorbents decreased as a result of NOM preloading due to site competition and/or pore/interstice blockage. However, among all adsorbents, GO was generally effected least from the NOM preloading for PNT, whereas there was not observed any trend of NOM competition with a specific adsorbent for TCE. In addition, SWCNT was generally affected most from the NOM preloading for TCE and there was not any trend for PNT. The overall results indicated that the fate and transport of organic contaminants by GNSs and CNTs type of nanoadsorbents and GACs in different natural systems will be affected by water quality parameters, characteristics of adsorbent, and properties of adsorbate. Copyright © 2016 Elsevier B.V. All rights reserved.

Rare earth elements and neodymium isotopes in sedimentary organic matter

Science.gov (United States)

Freslon, Nicolas; Bayon, Germain; Toucanne, Samuel; Bermell, Sylvain; Bollinger, Claire; Chéron, Sandrine; Etoubleau, Joel; Germain, Yoan; Khripounoff, Alexis; Ponzevera, Emmanuel; Rouget, Marie-Laure

2014-09-01

We report rare earth element (REE) and neodymium (Nd) isotope data for the organic fraction of sediments collected from various depositional environments, i.e. rivers (n = 25), estuaries (n = 18), open-ocean settings (n = 15), and cold seeps (n = 12). Sedimentary organic matter (SOM) was extracted using a mixed hydrogen peroxide/nitric acid solution (20%-H2O2-0.02 M-HNO3), after removal of carbonate and oxy-hydroxide phases with dilute hydrochloric acid (0.25 M-HCl). A series of experimental tests indicate that extraction of sedimentary organic compounds using H2O2 may be complicated occasionally by partial dissolution of sulphide minerals and residual carbonates. However, this contamination is expected to be minor for REE because measured concentrations in H2O2 leachates are about two-orders of magnitude higher than in the above mentioned phases. The mean REE concentrations determined in the H2O2 leachates for samples from rivers, estuaries, coastal seas and open-ocean settings yield relatively similar levels, with ΣREE = 109 ± 86 ppm (mean ± s; n = 58). The organic fractions leached from cold seep sediments display even higher concentration levels (285 ± 150 ppm; mean ± s; n = 12). The H2O2 leachates for most sediments exhibit remarkably similar shale-normalized REE patterns, all characterized by a mid-REE enrichment compared to the other REE. This suggests that the distribution of REE in leached sedimentary organic phases is controlled primarily by biogeochemical processes, rather than by the composition of the source from which they derive (e.g. pore, river or sea-water). The Nd isotopic compositions for organic phases leached from river sediments are very similar to those for the corresponding detrital fractions. In contrast, the SOM extracted from marine sediments display εNd values that typically range between the εNd signatures for terrestrial organic matter (inferred from the analysis of the sedimentary detrital fractions) and marine organic matter

Study on the effect of organic fertilizers on soil organic matter and enzyme activities of soil in forest nursery

Directory of Open Access Journals (Sweden)

Piaszczyk Wojciech

2017-09-01

Full Text Available The aim of the study was to assess the effects of organic fertilization on selected chemical properties of the soil and the activity of dehydrogenase and β-glucosidase in the soil of forest nursery. The main goal was to evaluate the role of organic fertilizers in carbon storage in the forest nursery soil. Sample plots were located in northern Poland in the Polanów Forest District on a forest nursery. Soil samples were collected from horizon 0–20 cm for laboratory analyzes. In soil samples pH, soil texture, and organic carbon, nitrogen, base cation contents, dehydrogenase activity and β-glucosidase activity were determined. The obtained results were used to evaluate the carbon storage. The results confirm the beneficial effect of the applied organic fertilizer on chemical properties of the soils under study and their biological activity. The applied organic fertilizers had an impact on increased accumulation of soil organic matter. In the soils investigated, there was an increase in the activity of such enzymes as dehydrogenases and β-glucosidase.

Multiscale organisation of organic matter associated with gold and uranium minerals in the Witwatersrand basin, South Africa

Energy Technology Data Exchange (ETDEWEB)

Smieja-Krol, Beata; Duber, Stanislaw [Faculty of Earth Science, University of Silesia, 60 Bedzinska St., 41-200 Sosnowiec (Poland); Rouzaud, Jean-Noel [Laboratoire de Geologie, Ecole Normale Superieure, 24, rue Lhomond, 75231 Paris Cedex 5 (France)

2009-03-01

Organic matter from the northern part of the Early Proterozoic Witwatersrand basin (Carbon Leader reef) was investigated using optical (OM) and transmission electron (TEM) microscopes, completed by XRD analysis. The multiscale organization (texture, microtexture, structure) of the organic matter was observed in order to gain information about the processes which affected organic material after its deposition in sediments. In the micrometre scale (optical microscope), the shape and size of the Reflectance Indicating Surface (RIS) of the organic matter were determined. The organic matter reveals a prevailing biaxial symmetry. The size of RIS is generally dependent on uranium and increases with increasing uranium concentration. Furthermore, it appears that more than one RIS is present within the scale of a single sample, each with a different symmetry and size. The presence of domains differing in organisation of the aromatic framework was confirmed by TEM observation in the DF mode. The aromatic skeleton of organic matter is composed of short, often crumpled, mostly isolated (non-stacked) polyaromatic layers whose fringe length corresponds to 3-16 aromatic rings. The data indicate reorganization of the polyaromatic organic matter structure under stress in high pressure and relatively low temperature conditions. The organic matter was in a solid state within the rocks before the pressure event. (author)

Coarse Particulate Organic Matter: Storage, Transport, and Retention

Energy Technology Data Exchange (ETDEWEB)

Tiegs, Scott [Oakland University, Rochester, MI; Lamberti, Gary A. [University of Notre Dame, IN; Entrekin, Sally A. [University of Central Arkansas; Griffiths, Natalie A. [ORNL

2017-08-01

Coarse particulate organic matter, or CPOM, is a basal energy and nutrient resource in many stream ecosystems and is provided by inputs from the riparian zone, incoming tributaries, and to a lesser extent from in-stream production. The ability of a stream to retain CPOM or slow its transport is critical to its consumption and assimilation by stream biota. In this chapter, we describe basic exercises to measure (1) the amount of CPOM in the streambed and (2) the retention of CPOM from standardized particle releases. We further describe advanced exercises that (1) experimentally enhance the retentiveness of a stream reach and (2) measure organic carbon transport and turnover (i.e., spiraling) in the channel.

Coarse Particulate Organic Matter: Storage, Transport, and Retention

Energy Technology Data Exchange (ETDEWEB)

Tiegs, Scott [Oakland University, Rochester, MI; Lamberti, Gary A. [University of Notre Dame, IN; Entrekin, Sally A. [University of Central Arkansas; Griffiths, Natalie A. [ORNL

2017-06-01

Coarse particulate organic matter, or CPOM, is a basal energy and nutrient resource in many stream ecosystems and is provided by inputs from the riparian zone, incoming tributaries, and to a lesser extent from in-stream production. The ability of a stream to retain CPOM or slow its transport is critical to its consumption and assimilation by stream biota. In this chapter, we describe basic exercises to measure (1) the amount of CPOM in the streambed and (2) the retention of CPOM from standardized particle releases. We further describe advanced exercises that (1) experimentally enhance the retentiveness of a stream reach and (2) measure organic carbon transport and turnover (i.e., spiraling) in the channel.

Mineral-associated organic matter: are we now on the right path to accurately measuring and modelling it?

Science.gov (United States)

Cotrufo, M. F.

2017-12-01

Mineral-associated organic matter (MAOM) is the largest and most persistent pool of carbon in soil. Understanding and correctly modeling its dynamic is key to suggest management practices that can augment soil carbon storage for climate change mitigation, as well as increase soil organic matter (SOM) stocks to support soil health on the long-term. In the Microbial Efficiency Mineral Stabilization (MEMS) framework we proposed that, contrary to what originally thought, this form of persistent SOM is derived from the labile components of plant inputs, through their efficient microbial processing. I will present results from several experiments using dual isotope labeling of plant inputs that largely confirm this opinion, and point to the key role of dissolved organic matter in MAOM formation, and to the dynamic nature of the outer layer of MAOM. I will also show how we are incorporating this understanding in a new SOM model, which uses physically defined measurable pools rather than turnover-defined pools to forecast C cycling in soil.

Organic matter in constructed soils from a coal mining area in southern Brazil

Energy Technology Data Exchange (ETDEWEB)

Dick, Deborah P.; Avila, Leticia G. [Universidade Federal do Rio Grande do Sul, Inst. de Quimica, Porto Alegre, RS (Brazil); Knicker, Heike [Technische Universitaet Muenchen, Lehrstuhl fuer Bodenkunde, Freising-Weihenstephan (Germany); Inda, Alberto V. Jr.; Giasson, Elvio; Bissani, Carlos A. [Universidade Federal do Rio Grande do Sul, Dept. de Ciencia do Solo, Porto Alegre, RS (Brazil)

2006-11-15

In southern Brazil, the landscape restoration after the exhaustion of open cast coal mines involves the filling of mine cavities with both pedogenic and geological material. The objective of this work was to determine the content and chemical composition of the organic matter of two constructed soils (24 years and 2 years) in a coal mining area in southern Brazil. An undisturbed Acrisol and geological material from three sites were also sampled. Samples were analyzed for carbon and nitrogen contents by dry combustion and for chemical composition of the organic matter by {sup 13} C NMR CPMAS and FTIR spectroscopies. Prior to the spectroscopic analyses, the samples were treated with 10% (m/m) hydrofluoric acid solution, which lead to a carbon enrichment in the sample of 2-46 times. The three coal samples were mainly composed of aromatic C (46-63%) and alkyl C (10-28%), and differed largely in the carbon content (18-312 g kg{sup -1}). The C/N ratio of 27 and the proportions of O-alkyl C (26%) and aromatic C (29%) found in the native soil (18 g C kg{sup -1} soil) suggest a coal contamination of the native site. The proportions of O/N-alkyl C (15-17%), alkyl C (22-23%) and aromatic C (39-41%) observed in the organic matter of the A1 horizon of the two constructed soils were intermediate to those of the coal samples and the native soil. In the younger constructed soil the proportion of O/N-alkyl diminished and that of aromatic C increased with depth, whereas in the older constructed soil this trend was less evident. Our results show that, during the 24 years after site reconstruction, the input of vegetation residues diluted the proportion of recalcitrant organic matter. The aromaticity index calculated from the FTIR data (I{sub 1620} /I{sub 2920}) correlated positively with the aryl C/alkyl C ratio, obtained from the NMR data, evidencing the applicability of the FTIR index for geological and coal contaminated samples. (Author)

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...

Use of isotopes in organic matter studies: a discussion illustrated by recent applications

International Nuclear Information System (INIS)

Warembourg, F.R.

1982-01-01

After a presentation of the various concepts leading to the advantageous use of isotope tracers in soil organic matter and related studies, a discussion is proposed around three main types of methods which are related to the time scale of the processes occurring in the soil organic matter transformations. Examples help to illustrate the purpose. Static methods describing the state of soil organic matter such as carbon dating. Long term dynamic studies involving the use of labelled plant materials and their applications in situ. Short term dynamic studies as an insight into the short term lived processes such as biotic and abiotic energetic activivation, flushes, priming effect, nitrogen fixation. More than an exhaustive enumeration of the litterature, the main objective of this presentation will tend to be a comprehensive analysis of the many problems arising from the study of soil activities and of the modern approaches of investigation. (Author) [pt

Influence of biochar and plant growth on organic matter dynamics in a reclaimed mine residue

Science.gov (United States)

Moreno-Barriga, Fabián; Díaz, Vicente; Alberto, Jose; Faz, Ángel; Zornoza, Raúl

2016-04-01

This study aims at assessing the impact of biochar and marble waste amendment and the development of vegetation in acidic mine wastes on organic matter dynamics. For this purpose, a mine residue was collected in a tailing pond from the Sierra Minera of Cartagena-La Unión (SE Spain), and a greenhouse experiment was established for 120 days. Marble waste (MW) was added in a rate of 200 g kg-1 as a source of calcium carbonate to increase the pH from 3 to 7.5-8 (average pH in the native soils of the area). We added biochar as a source of organic carbon and nutrients, in two different rates, 50 g kg-1 (BC1) and 100 g kg-1 (BC2). To assess the influence of vegetation growth on the creation of a technosoil from mine residues and its impact on organic matter dynamics, the plant species Piptatherum miliaceum (PM) was planted in half the pots with the different amendments. Thus, five treatments were established: unamended and unplanted control (CT), BC1, BC2, BC1+PM and BC2+PM. Results showed that the different treatments had no significant effect on aggregates stability, microbial biomass carbon and the emission of N2O and CH4. So, it seems that longer periods are needed to increase the stability of aggregates and microbial populations, since even the combined use of biochar, marble waste and vegetation was not enough to increase these properties in 120 days. Nonetheless, it was positive that the addition of biochar and the release of root exudates did not trigger the emission of greenhouse gases. Organic carbon significantly increased with the addition of biochar, with values similar to the dose applied, indicating high stability and low mineralization of the amendment. The addition of amendments significantly increased arylesterase activity, while the growth of the plant was needed to significantly increase β-glucosidase activity. The soluble carbon significantly decreased in BC1 and BC2 with regards to CT, while no significant differences were observed among CT and

Sources and export of particle-borne organic matter during a monsoon flood in a catchment of northern Laos

Science.gov (United States)

Gourdin, E.; Huon, S.; Evrard, O.; Ribolzi, O.; Bariac, T.; Sengtaheuanghoung, O.; Ayrault, S.

2015-02-01

The yields of the tropical rivers of Southeast Asia supply large quantities of carbon to the ocean. The origin and dynamics of particulate organic matter were studied in the Houay Xon River catchment located in northern Laos during the first erosive flood of the rainy season in May 2012. This cultivated catchment is equipped with three successive gauging stations draining areas ranging between 0.2 and 11.6 km2 on the main stem of the permanent stream, and two additional stations draining 0.6 ha hillslopes. In addition, the sequential monitoring of rainwater, overland flow and suspended organic matter compositions was conducted at the 1 m2 plot scale during a storm. The composition of particulate organic matter (total organic carbon and total nitrogen concentrations, δ13C and δ15N) was determined for suspended sediment, soil surface (top 2 cm) and soil subsurface (gullies and riverbanks) samples collected in the catchment (n = 57, 65 and 11, respectively). Hydrograph separation of event water was achieved using water electric conductivity and δ18O measurements for rainfall, overland flow and river water base flow (n = 9, 30 and 57, respectively). The composition of particulate organic matter indicates that upstream suspended sediments mainly originated from cultivated soils labelled by their C3 vegetation cover (upland rice, fallow vegetation and teak plantations). In contrast, channel banks characterized by C4 vegetation (Napier grass) supplied significant quantities of sediment to the river during the flood rising stage at the upstream station as well as in downstream river sections. The highest runoff coefficient (11.7%), sediment specific yield (433 kg ha-1), total organic carbon specific yield (8.3 kg C ha-1) and overland flow contribution (78-100%) were found downstream of reforested areas planted with teaks. Swamps located along the main stream acted as sediment filters and controlled the composition of suspended organic matter. Total organic carbon

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

Influence of long-term land use (arable and forest) and soil mineralogy on organic carbon stocks as well as composition and stability of soil organic matter

Science.gov (United States)

Kaiser, M.; Ellerbrock, R. H.; Wulf, M.; Dultz, S.; Hierath, C.; Sommer, M.

2009-04-01

The function of soils to sequester organic carbon (OC) and their related potential to mitigate the greenhouse effect is strongly affected by land use and soil mineralogy. This study is aimed to clarify long-term impacts of arable and forest land use as well as soil mineralogy on topsoil soil organic carbon (SOC) stocks as well as soil organic matter (SOM) composition and stability. Topsoil samples were taken from deciduous forest and adjacent arable sites (within Germany) that are continuously used for more than 100 years. The soils are different in genesis (Albic and Haplic Luvisol (AL, HL), Colluvic and Haplic Regosol (CR, HR), Haplic and Vertic Cambisol (HC, VC), Haplic Stagnosol (HSt)). First, particulate and water soluble organic matter were separated from the topsoil samples (Ap and Ah horizons). From the remaining solid extraction residues the Na-pyrophosphate soluble organic matter fractions (OM(PY)) were extracted, analysed for its OC content (OC(PY)) and characterized by FTIR spectroscopy and 14C analyses. The SOC stocks calculated for 0-40 cm depth are in general larger for the forest as compared to the adjacent arable soils (except VC). The largest difference between forest and arable topsoils was detected for the HR site (5.9 kg m-2) and seemed to be caused by a two times larger stock of exchangeable Ca of the forest topsoil. For the arable topsoils multiple regression analyses indicate a strong influence of clay, oxalate soluble Al and pyrophosphate soluble Mg on the content of OC(PY) weighted with its C=O content. Such relation is not found for the forest topsoils. Further, a positive relation between Δ14C values of OM(PY) and the following independent variables: (i) specific mineral surface area, (ii) relative C=O group content in OM(PY) and (iii) soil pH is found for the arable topsoils (pH 6.7 - 7.5) suggesting an increase in OM(PY) stability with increasing interactions between OM(PY) and soil mineral surfaces via cation bridging. A similar

CO2 Losses from Terrestrial Organic Matter through Photodegradation

Science.gov (United States)

Rutledge, S.; Campbell, D. I.; Baldocchi, D. D.; Schipper, L. A.

2010-12-01

Net ecosystem exchange (NEE) is the sum of CO2 uptake by plants and CO2 losses from both living plants and dead organic matter. In all but a few ecosystem scale studies on terrestrial carbon cycling, losses of CO2 from dead organic matter are assumed to be the result of microbial respiration alone. Here we provide evidence for an alternative, previously largely underestimated mechanism for ecosystem-scale CO2 emissions. The process of photodegradation, the direct breakdown of organic matter by solar radiation, was found to contribute substantially to the ecosystem scale CO2 losses at both a bare peatland in New Zealand, and a summer-dead grassland in California. Comparisons of daytime eddy covariance (EC) data with data collected at the same time using an opaque chamber and the CO2 soil gradient technique, or with night-time EC data collected during similar moisture and temperature conditions were used to quantify the direct effect of exposure of organic matter to solar radiation. At a daily scale, photodegradation contributed up to 62% and 92% of summer mid-day CO2 fluxes at the de-vegetated peatland and at the grassland during the dry season, respectively. Irradiance-induced CO2 losses were estimated to be 19% of the total annual CO2 loss at the peatland, and almost 60% of the dry season CO2 loss at the grassland. Small-scale measurements using a transparent chamber confirmed that CO2 emissions from air-dried peat and grass occurred within seconds of exposure to light when microbial activity was inhibited. Our findings imply that photodegradation could be important for many ecosystems with exposed soil organic matter, litter and/or standing dead material. Potentially affected ecosystems include sparsely vegetated arid and semi-arid ecosystems (e.g. shrublands, savannahs and other grasslands), bare burnt areas, agricultural sites after harvest or cultivation (especially if crop residues are left on the surface), deciduous forests after leaf fall, or ecosystems

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.

Characteristics of sedimentary organic matter in coastal and depositional areas in the Baltic Sea

Science.gov (United States)

Winogradow, A.; Pempkowiak, J.

2018-05-01

As organic matter (OM) is readily mineralized to carbon dioxide (Smith and Hollibangh, 1993; Emerson and Hedges, 2002; Szymczycha et al., 2017) it has a direct link to the carbon dioxide abundance in seawater and an indirect influence on the carbon dioxide concentration in the atmosphere (Emerson and Hedges, 2002; Schulz and Zabel, 2006). OM is a quantitatively minor yet important component of seawater. OM in seawater can originate from internal sources (marine, or planktonic, or autochthonous OM) or external sources (terrestrial, or allochtonous OM) (Maksymowska et al., 2000; Emerson and Hedges, 2002; Turnewitsch et al., 2007; Arndt et al., 2013). It is commonly divided into two fractions: dissolved (DOM) and particulate (POM). Organic carbon (OC) is, most often, used as a measure of OM.

Some aspects of the development of the Vaal Reef uranium-gold carbon seams, Witwatersrand sequence: organic geochemical and microbiological considerations

International Nuclear Information System (INIS)

Zumberge, J.E.; Nagy, B.; Nagy, L.A.

1981-01-01

The solvent-insoluble organic matter (kerogen) that is the predominant syngenetic component of the Vaal Reef carbon seams was analyzed by combined high-vacuum pyrolysis gas-chromatography mass spectrometry, combined electron microprobe-scanning electron microscopy and electron paramagnetic resonance spectroscopy. The pyrolysis results indicate that the Vaal Reef carbon is a random polymer-type matter consisting mainly of aromatic and short-chain aliphatic hydrocarbons, as well as aromatic and other organic-sulfur constituents. Scanning electron microscopy revealed coccoid and filamentous microstructures in the carbonaceous seams. These structures are conceivably of biological affinity and may be fossil blue-green algae and (or) bacteria. Gold is often concentrated at the interfaces of admixed clay-carbon microenvironments. This implies physical and chemical interactions between clays and organic matter conducive to the entrapment of detrital gold during deposition and the crystallization of colloidal/dissolved gold in the carbon seams. High concentrations of organic free radicals (molecules with unpaired electrons) in the carbonaceous matter, deduced from electron paramagnetic resonance spectroscopy, suggest that radiation emitted from uranium played a unique role in the reconstitution and polymerization of the progenitor biochemicals

Adsorption of clofibric acid and ketoprofen onto powdered activated carbon: effect of natural organic matter.

Science.gov (United States)

Gao, Yaohuan; Deshusses, Marc A

2011-12-01

The adsorption of two acidic pharmaceutically active compounds (PhACs), clofibric acid and ketoprofen, onto powdered activated carbon (PAC) was investigated with a particular focus on the influence of natural organic matter (NOM) on the adsorption of the PhACs. Suwannee River humic acids (SRHAs) were used as a substitute for NOM. Batch adsorption experiments were conducted to obtain adsorption kinetics and adsorption isotherms with and without SRHAs in the system. The adsorption isotherms and adsorption kinetics showed that the adsorption ofclofibric acid was not significantly affected by the presence of SRHAs at a concentration of 5 mg (as carbon) L(-1). An adsorption capacity of 70 to 140 mg g(-1) was observed and equilibrium was reached within 48 h. In contrast, the adsorption of ketoprofen was markedly decreased (from about 120 mg g(-1) to 70-100 mg g(-1)) in the presence of SRHAs. Higher initial concentrations of clofibric acid than ketoprofen during testing may explain the different behaviours that were observed. Also, the more hydrophobic ketoprofen molecules may have less affinity for PAC when humic acids (which are hydrophilic) are present. The possible intermolecular forces that could account for the different behaviour of clofibric acid and ketoprofen adsorption onto PAC are discussed. In particular, the relevance of electrostatic forces, electron donor-acceptor interaction, hydrogen bonding and London dispersion forces are discussed

Soil organic matter dynamics and CO2 fluxes in relation to landscape scale processes: linking process understanding to regional scale carbon mass-balances

Science.gov (United States)

Van Oost, Kristof; Nadeu, Elisabet; Wiaux, François; Wang, Zhengang; Stevens, François; Vanclooster, Marnik; Tran, Anh; Bogaert, Patrick; Doetterl, Sebastian; Lambot, Sébastien; Van wesemael, Bas

2014-05-01

In this paper, we synthesize the main outcomes of a collaborative project (2009-2014) initiated at the UCL (Belgium). The main objective of the project was to increase our understanding of soil organic matter dynamics in complex landscapes and use this to improve predictions of regional scale soil carbon balances. In a first phase, the project characterized the emergent spatial variability in soil organic matter storage and key soil properties at the regional scale. Based on the integration of remote sensing, geomorphological and soil analysis techniques, we quantified the temporal and spatial variability of soil carbon stock and pool distribution at the local and regional scales. This work showed a linkage between lateral fluxes of C in relation with sediment transport and the spatial variation in carbon storage at multiple spatial scales. In a second phase, the project focused on characterizing key controlling factors and process interactions at the catena scale. In-situ experiments of soil CO2 respiration showed that the soil carbon response at the catena scale was spatially heterogeneous and was mainly controlled by the catenary variation of soil physical attributes (soil moisture, temperature, C quality). The hillslope scale characterization relied on advanced hydrogeophysical techniques such as GPR (Ground Penetrating Radar), EMI (Electromagnetic induction), ERT (Electrical Resistivity Tomography), and geophysical inversion and data mining tools. Finally, we report on the integration of these insights into a coupled and spatially explicit model and its application. Simulations showed that C stocks and redistribution of mass and energy fluxes are closely coupled, they induce structured spatial and temporal patterns with non negligible attached uncertainties. We discuss the main outcomes of these activities in relation to sink-source behavior and relevance of erosion processes for larger-scale C budgets.

Laboratory Calibration Studies in Support of ORGANICS on the International Space Station: Evolution of Organic Matter in Space

Science.gov (United States)

Ruiterkamp, R.; Ehrenfreund, P.; Halasinski, T.; Salama, F.; Foing, B.; Schmidt, W.

2002-01-01

This paper describes the scientific overview and current status of ORGANICS an exposure experiment performed on the International Space Station (ISS) to study the evolution of organic matter in space (PI: P. Ehrenfreund), with supporting laboratory experiments performed at NASA Ames. ORGANICS investigates the chemical evolution of samples submitted to long-duration exposure to space environment in near-Earth orbit. This experiment will provide information on the nature, evolution, and survival of carbon species in the interstellar medium (ISM) and in solar system targets.

Sources, Fate and Distribution of Organic Matter on the Western Adriatic Continental Shelf, Italy

International Nuclear Information System (INIS)

Tesi, Tommaso; Miserocchi, Stefano; Langone, Leonardo; Boni, Laurita; Guerrini, Franca

2006-01-01

In the framework of the EUROSTRATAFORM projects, a multidisciplinary research was focused on processes that involve transport and deposition of riverine material in the Adriatic Sea. The aim of our contribution was to increase a more complete understanding of organic matter deposition on the Adriatic shelf, also taking into account the role of Apennine rivers beyond the Po influence. In order to characterize origin, fate and variability of sedimentary organic carbon we utilized elemental and stable carbon isotope data in surficial sediments along shallow cross-shelf transects on the western Adriatic shelf

Source and composition of surface water dissolved organic matter (DOM) and the effect of flood events on the organic matter cycling

Science.gov (United States)

Bondar-Kunze, Elisabeth; Welti, Nina; Tritthart, Michael; Baker, Andrew; Pinay, Gilles; Hein, Thomas

2014-05-01

Floodplains are often simultaneously affected by land use change, river regulation and loss of hydrological dynamics which alter the surface water connectivity between floodplain and river main channel. These alterations can have significant impacts on the sources of organic matter and their degradation and thus, the carbon cycling of riverine landscapes. Although floodplains are known to be important sources of dissolved organic matter (DOM) within watersheds, reduced hydrological connectivity impair their role. The key questions of our research were to determine i) to what extent the degree of connection between the Danube River and its floodplain controlled the DOM composition with its backwater systems, and ii) what were the effects of the DOM changes on carbon cycling in floodplains during two flood events with different magnitude? In this study we report on the variations in DOM spectrophotometric properties of surface waters in different connected floodplain areas and during two flood events of different magnitude in a section of the Alluvial Zone National Park of the Danube River downstream Vienna, Austria. Two backwater floodplain systems were studied, one backwater system mostly disconnected from the fluvial dynamics except during high flood events (Lower Lobau) and the second one, recently restored and connected even during mean flow conditions (Orth). Fluorescence excitation-emission matrix (EEM) spectrophotometry and water chemical analyses were applied to investigate the DOM dynamics. In both backwater systems 15 sites were sampled monthly for two years and every second day during a flood event.

Effect of organic acids traces on the carbon steel corrosion behavior

International Nuclear Information System (INIS)

Stefanescu, D.; Radulescu; Mogosan, S.

2009-01-01

There are many different ways in which organic matter may get in water-steam cycles. One important pathway is constituted by organic matter admitted into the system by chemical make-up water under standard operation conditions (without inverse osmosis). The high molecular weight organic matter, in particularly polysaccharides are broken in organic acids, in particular acetic and formic acid. This paper presents an overview of the investigations undertaken referring to the behavior SA106 gr. B mild steel in secondary circuit aqueous environment contaminated with formic and acetic acid traces. The samples were filmed in static autoclaves in operation conditions of secondary circuit, in contaminated environment and after that they were investigated using metallographic microscopy and SEM. In addition, an electrochemical technique videlicet impedance spectroscopy (EIS) was used to investigate the corrosion behavior of SA106 gr. B carbon steel in secondary circuit medium contaminated with formic and acetic acid traces. (authors)

A 200 year sedimentary record of progressive eutrophication in lake Greifen (Switzerland): Implications for the origin of organic-carbon-rich sediments

Science.gov (United States)

Hollander, David J.; McKenzie, Judith A.; Lo Ten Haven, H.

1992-09-01

Over the past 200 years Lake Greifen, a small lake in northeastern Switzerland, has undergone dramatic changes in primary productivity and eutrophication due to increased nutrient supply from agricultural activity and industrialization. A 40 year historical record of the water-column chemistry indicates that productivity and eutrophication reached a maximum in 1974, after which stricter regulations on the input of nutrients resulted in a progressive decrease. Collected cores show the sedimentary expression of this anthropogenically induced eutrophication by a well-developed annual sedimentation and by enhanced values of total organic carbon, organic-carbon accumulation rates, and hydrogen indices (HI) of the kerogens. Analyses of the carbon isotopic composition of sedimentary carbonates and organic matter reveal that the fractionation between these two phases varies with the HI of kerogens. This observation is explicable in terms of changing productivity and preservation of the organic matter, and the CO2(aq) budget of the water body. We propose that if high primary productivity were primarily responsible for the preservation and accumulation of organic matter, then a negative correlation will occur between Δδ13Ccalcite-organic matter (Δδ13Ccal-om) and HI values. In an environment with relatively low to moderate productivity but with bottom-water anoxia, a positive correlation will exist between Δδ13Ccal-om and HI values. This study of Lake Greifen has implications for understanding paleoenvironmental controls on ancient organic-carbon-rich sediments.

Land use and soil organic matter in South Africa 1: A review on spatial variability and the influence of rangeland stock production

Directory of Open Access Journals (Sweden)

Pearson N.S. Mnkeni

2011-05-01

Full Text Available Degradation of soil as a consequence of land use poses a threat to sustainable agriculture in South Africa, resulting in the need for a soil protection strategy and policy. Development of such a strategy and policy require cognisance of the extent and impact of soil degradation processes. One of the identified processes is the decline of soil organic matter, which also plays a central role in soil health or quality. The spatial variability of organic matter and the impact of grazing and burning under rangeland stock production are addressed in this first part of the review. Data from uncoordinated studies showed that South African soils have low organic matter levels. About 58% of soils contain less than 0.5% organic carbon and only 4% contain more than 2% organic carbon. Furthermore, there are large differences in organic matter content within and between soil forms, depending on climatic conditions, vegetative cover, topographical position and soil texture. A countrywide baseline study to quantify organic matter contents within and between soil forms is suggested for future reference. Degradation of rangeland because of overgrazing has resulted in significant losses of soil organic matter, mainly as a result of lower biomass production. The use of fire in rangeland management decreases soil organic matter because litter is destroyed by burning. Maintaining or increasing organic matter levels in degraded rangeland soils by preventing overgrazing and restricting burning could contribute to the restoration of degraded rangelands. This restoration is of the utmost importance because stock farming uses the majority of land in South Africa.

Long-term citrus organic farming strategy results in soil organic matter recovery

Science.gov (United States)

Novara, Agata; Pereira, Paulo; Barone, Ettore; Giménez Morera, Antonio; Keesstra, Saskia; Gristina, Luciano; Jordán, Antonio; Parras-Alcantara, Luis; Cerdà, Artemi

2017-04-01

.: The significance of soils and soil science towards realization of the United Nations Sustainable Development Goals, SOIL, 2, 111-128, doi:10.5194/soil-2-111-2016, 2016. Keesstra, S.D., Geissen, V., van Schaik, L., Mosse., K., Piiranen, S., 2012. Soil as a filter for groundwater quality. Current Opinions in Environmental Sustainability 4, 507-516. doi:10.1016/j.cosust.2012.10.007 Laudicina, V. A., A. Novara, V. Barbera, M. Egli, and L. Badalucco. 2015. Long-Term Tillage and Cropping System Effects on Chemical and Biochemical Characteristics of Soil Organic Matter in a Mediterranean Semiarid Environment. Land Degradation and Development 26 (1): 45-53. doi:10.1002/ldr.2293. Mol, G., Keesstra, S.D., 2012. Editorial: Soil science in a changing world. Current Opinions in Environmental Sustainability 4: 473-477. Novara, A., L. Gristina, M. B. Bodì, and A. Cerdà. 2011. The Impact of Fire on Redistribution of Soil Organic Matter on a Mediterranean Hillslope Under Maquia Vegetation Type. Land Degradation and Development 22 (6): 530-536. doi:10.1002/ldr.1027. Parras-Alcántara, L., B. Lozano-García, E. C. Brevik, and A. Cerdá. 2015. Soil Organic Carbon Stocks Assessment in Mediterranean Natural Areas: A Comparison of Entire Soil Profiles and Soil Control Sections. Journal of Environmental Management 155: 219-228. doi:10.1016/j.jenvman.2015.03.039. Parras-Alcántara, L., B. Lozano-García, S. Keesstra, A. Cerdà, and E. C. Brevik. 2016. Long-Term Effects of Soil Management on Ecosystem Services and Soil Loss Estimation in Olive Grove Top Soils. Science of the Total Environment. doi:10.1016/j.scitotenv.2016.07.016.

Changes of Organic Carbon Quantity and Quality in Temperate Forest Soils

Science.gov (United States)

Kühnel, Anna; Satwika Lestari, Annisa; Schubert, Alfred; Wiesmeier, Martin; Spörlein, Peter; Schilling, Bernd; Kögel-Knabner, Ingrid

2017-04-01

Climate change will have profound impacts on organic matter stocks and thus on the functionality of soils. Soil organic carbon (SOC) content in soil is mainly regulated by the fluxes of organic matter which are highly associated with the aboveground and root litter production and their decompositions into CO2 by soil microorganism. The predicted rising temperatures in Bavaria might lead to an increased decomposition and release of soil carbon into the atmosphere, which would deteriorate a number of important soil functions. Here, we present an assessment of SOC stocks in three temperate forest sites over the last 30 years. Soil to a depth of 30 cm was analysed with density fractionation to evaluate SOC stocks and distribution in different pools. Additionally, tree-aboveground organic carbon (OC) stocks were measured to assess their influence on SOC. SOC stocks decreased between 1988 and 2004 and increased between 2004 and 2016. OC changes of litter + O layer and mineral soil differed. Highest changes of SOC occurred in the light fractions, followed by the mineral fractions. Tree-aboveground biomass, stand composition, and changing climate had an influence on SOC stocks. Precipitation change was correlated with the litter + O layer OC stocks. Further studies on the changes of each SOC fraction and the influence of other edaphic factors are needed to better understand the changes in SOC stocks and quality.

The destruction of organic matter

CERN Document Server

Gorsuch, T T

1970-01-01

International Series of Monographs in Analytical Chemistry, Volume 39: The Destruction of Organic Matter focuses on the identification of trace elements in organic compounds. The monograph first offers information on the processes involved in the determination of trace elements in organic matters, as well as the methods not involving complete destruction of these elements. The text surveys the sources of errors in the processes responsible in pinpointing elements in organic compounds. These processes include sampling, disruption of the samples, manipulation, and measurements. The book

Organic biomarkers to describe the major carbon inputs and cycling of organic matter in the central Great Barrier Reef region

Science.gov (United States)

Burns, Kathryn; Brinkman, Diane

2011-06-01

Controversy surrounds the sources and transport of land derived pollutants in the Great Barrier Reef ecosystem because there is insufficient knowledge of the mechanism of movement of organic contaminants and the cycling of organic matter in this dynamic system. Thus a sediment and sediment trap study was used to describe the composition of resuspended and surface sediments in the south central Great Barrier Reef and its lagoon. This region is characterised by strong tides (6-8 m at Mackay) and trade winds regularly about 15-20 knots. A series of organic biomarkers detailed the cyclical processes of sediment resuspension, recolonising with marine algae and bacteria, packaging into zooplankton faecal pellets and resettlement to sediments where the organics undergo further diagenesis. With each cycle the inshore sediments are diluted with CaCO 3 reef sediments and moved further offshore with the strong ebb tide currents. This results in transport of land derived materials offshore and little storage of organic materials in the lagoon or reef sediments. These processes were detailed by inorganic measurements such as %CaCO 3 and Al/Ca ratios, and by the compositions of hydrocarbon, sterol, alcohol, and fatty acid lipid fractions. Persistent contaminants such as coal dust from a coastal loading facility can be detected in high concentration inshore and decreasing out to the shelf break at 180 m approximately 40 nautical miles offshore. The normal processes would likely be amplified during cyclonic and other storms. The lipids show the sources of carbon to include diatoms and other phytoplankton, creanaerchaeota, sulfate reducing and other bacteria, land plants including mangrove leaves, plus coal dust and other petroleum contaminants.

Examining organic carbon transport by the Orinoco River using SeaWiFS imagery

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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.

Relative age and age sequence of fractions of soil organic matter

International Nuclear Information System (INIS)

Scharpenseel, H.W.

1975-01-01

Natural radiocarbon measurements on soil fractions provide information regarding the chances of separating the ''old biologically inert carbon'' out of samples of recent soil material. Beyond this, the relative fraction ages are scrutinized for the sequential order of the origin of the fractions within the biosynthetic reaction chain of soil humic matter. Among all fractions compared (classic humic matter fractionation by alkali and acid treatment; successive extraction with organic solvents of increasing polarity; separation according to particle size by Sephadex gel filtration; hydrolysis residue) the 6 n HCl hydrolysis residue shows the most consistent significant age increment. Repeated exhaustive hydrolysis treatment of the same sample material is still pending. All other fraction types indicate an age pattern under strong predetermination by method of origin, e.g., existence or lack of hydromorphy, without an evident enrichment of the ''old biologically inert carbon''. Among the organic extracts, no persistent age hierarchy is noticeable, whereas the classical fractions follow an age sequence mainly parallel to an increase of the molecular weight. Hymatomelanic acids appear rejuvenated by relics of recent carbon derived from the extractant ethanol. Grey humic acids are older than the brown humic acids, humines from fully terrestrial soil environment are older than humic acids, while in hydromorphic soils, cold alkali insoluble young C-compounds seem to be conserved which are liable to falsify rejuvenation of the humines

Sources and turnover of organic carbon and methane in fjord and shelf sediments off northern Norway

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Sauer, Simone; Hong, Wei-Li; Knies, Jochen; Lepland, Aivo; Forwick, Matthias; Klug, Martin; Eichinger, Florian; Baranwal, Soma; Crémière, Antoine; Chand, Shyam; Schubert, Carsten J.

2016-10-01

To better understand the present and past carbon cycling and transformation processes in methane-influenced fjord and shelf areas of northern Norway, we compared two sediment cores from the Hola trough and from Ullsfjorden. We investigated (1) the organic matter composition and sedimentological characteristics to study the sources of organic carbon (Corg) and the factors influencing Corg burial, (2) pore water geochemistry to determine the contribution of organoclastic sulfate reduction and methanogenesis to total organic carbon turnover, and (3) the carbon isotopic signature of hydrocarbons to identify the carbon transformation processes and gas sources. High sedimentation and Corg accumulation rates in Ullsfjorden support the notion that fjords are important Corg sinks. The depth of the sulfate-methane-transition (SMT) in the fjord is controlled by the supply of predominantly marine organic matter to the sediment. Organoclastic sulfate reduction accounts for 60% of the total depth-integrated sulfate reduction in the fjord. In spite of the presence of ethane, propane, and butane, we suggest a purely microbial origin of light hydrocarbons in the sediments based on their low δ13C values. In the Hola trough, sedimentation and Corg accumulation rates changed during the deglacial-to-post-glacial transition from approximately 80 cm ka-1 to erosion at present. Thus, Corg burial in this part of the shelf is presently absent. Low organic matter content in the sediment and low rates of organoclastic sulfate reduction (only 3% of total depth-integrated sulfate reduction) entail that the shallow depth of the SMT is controlled mostly by ascending thermogenic methane from deeper sources.

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.

A review: Potential and challenges of biologically activated carbon to remove natural organic matter in drinking water purification process.

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Korotta-Gamage, Shashika Madushi; Sathasivan, Arumugam

2017-01-01

The use of biologically activated carbon (BAC) in drinking water purification is reviewed. In the past BAC is seen mostly as a polishing treatment. However, BAC has the potential to provide solution to recent challenges faced by water utilities arising from change in natural organic matter (NOM) composition in drinking water sources - increased NOM concentration with a larger fraction of hydrophilic compounds and ever increasing trace level organic pollutants. Hydrophilic NOM is not removed by traditional coagulation process and causes bacterial regrowth and increases disinfection by-products (DBPs) formation during disinfection. BAC can offer many advantages by removing hydrophilic fraction and many toxic and endocrine compounds which are not otherwise removed. BAC can also aid the other downstream processes if used as a pre-treatment. Major drawback of BAC was longer empty bed contact time (EBCT) required for an effective NOM removal. This critical review analyses the strategies that have been adopted to enhance the biological activity of the carbon by operational means and summarises the surface modification methods. To maximize the benefit of the BAC, a rethink of current treatment plant configuration is proposed. If the process can be expedited and adopted appropriately, BAC can solve many of the current problems. Copyright © 2016 Elsevier Ltd. All rights reserved.

Increased nitrogen availability counteracts climatic change feedback from increased temperature on boreal forest soil organic matter degradation

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Erhagen, Bjorn; Nilsson, Mats; Oquist, Mats; Ilstedt, Ulrik; Sparrman, Tobias; Schleucher, Jurgen

2014-05-01

Over the last century, the greenhouse gas concentrations in the atmosphere have increased dramatically, greatly exceeding pre-industrial levels that had prevailed for the preceding 420 000 years. At the same time the annual anthropogenic contribution to the global terrestrial nitrogen cycle has increased and currently exceeds natural inputs. Both temperature and nitrogen levels have profound effects on the global carbon cycle including the rate of organic matter decomposition, which is the most important biogeochemical process that returns CO2 to the atmosphere. Here we show for the first time that increasing the availability of nitrogen not only directly affects the rate of organic matter decomposition but also significantly affects its temperature dependence. We incubated litter and soil organic matter from a long-term (40 years) nitrogen fertilization experiment in a boreal Scots pine (Pinus silvestris L.) forest at different temperatures and determined the temperature dependence of the decomposition of the sample's organic matter in each case. Nitrogen fertilization did not affect the temperature sensitivity (Q10) of the decomposition of fresh plant litter but strongly reduced that for humus soil organic matter. The Q10 response of the 0-3 cm soil layer decreased from 2.5±0.35 to an average of 1.9±0.21 over all nitrogen treatments, and from 2.2±0.19 to 1.6±0.16 in response to the most intense nitrogen fertilization treatment in the 4-7 cm soil layer. Long-term nitrogen additions also significantly affected the organic chemical composition (as determined by 13C CP-MAS NMR spectroscopy) of the soil organic matter. These changes in chemical composition contributed significantly (p<0.05) to the reduced Q10 response. These new insights into the relationship between nitrogen availability and the temperature sensitivity of organic matter decomposition will be important for understanding and predicting how increases in global temperature and rising anthropogenic

Distribution and sources of sedimentary organic matter in a tropical estuary, south west coast of India (Cochin estuary): A baseline study

International Nuclear Information System (INIS)

Gireeshkumar, T.R.; Deepulal, P.M.; Chandramohanakumar, N.

2013-01-01

Highlights: ► We report δ 13 C and δ 15 N values of sedimentary organic matter from the Cochin estuary. ► δ 13 C and δ 15 N values ranged from −27.5‰ to −21.7‰ and δ 15 N 3.1–6.7‰ respectively. ► Organic matter is found to be mixture terrestrial and marine derived materials. ► The δ 15 N values displayed a complex behavior in the study region. ► The fraction of terrestrial derived organic matter was estimated. -- Abstract: Surface sediments samples were collected from 9 stations of the Cochin estuary during the monsoon, post-monsoon and pre-monsoon seasons and were analyzed for grain size, total organic carbon (OC), total nitrogen (TN) and stable isotopic ratios of carbon (δ 13 C) and nitrogen (δ 15 N) to identify major sources of organic matter in surface sediments. Sediment grain size is found to be the key factor influencing the organic matter accumulation in surface sediments. The δ 13 C values ranges from −27.5‰ to −21.7‰ in surface sediments with a gradual increase from inner part of the estuary to the seaward side that suggest an increasing contribution of marine autogenous organic matter towards the seaward side. The δ 15 N value varies between 3.1‰ and 6.7‰ and it exhibits complex spatial and seasonal distributions in the study area. It is found that the dynamic cycling of nitrogen through various biogeochemical and organic matter degradation processes modifies the OC/TN ratios and δ 15 N to a considerable degree. The fraction of terrestrial organic matter in the total organic matter pool ranges from 13% to 74% in the surface sediments as estimated by δ 13 C based two end member mixing model

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

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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

Direct and indirect controls on organic matter decomposition in four coastal wetland communities along a landscape salinity gradient

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Stagg, Camille L.; Baustian, Melissa M.; Perry, Carey L.; Carruthers, Tim J.B.; Hall, Courtney T.

2018-01-01

Coastal wetlands store more carbon than most ecosystems globally. As sea level rises, changes in flooding and salinity will potentially impact ecological functions, such as organic matter decomposition, that influence carbon storage. However, little is known about the mechanisms that control organic matter loss in coastal wetlands at the landscape scale. As sea level rises, how will the shift from fresh to salt-tolerant plant communities impact organic matter decomposition? Do long-term, plant-mediated, effects of sea-level rise differ from direct effects of elevated salinity and flooding?We identified internal and external factors that regulated indirect and direct pathways of sea-level rise impacts, respectively, along a landscape-scale salinity gradient that incorporated changes in wetland type (fresh, oligohaline, mesohaline and polyhaline marshes). We found that indirect and direct impacts of sea-level rise had opposing effects on organic matter decomposition.Salinity had an indirect effect on litter decomposition that was mediated through litter quality. Despite significant variation in environmental conditions along the landscape gradient, the best predictors of above- and below-ground litter decomposition were internal drivers, initial litter nitrogen content and initial litter lignin content respectively. Litter decay constants were greatest in the oligohaline marsh and declined with increasing salinity, and the fraction of litter remaining (asymptote) was greatest in the mesohaline marsh. In contrast, direct effects of salinity and flooding were positive. External drivers, salinity and flooding, stimulated cellulytic activity, which was highest in the polyhaline marsh.Synthesis. Our results indicate that as sea level rises, initial direct effects of salinity will stimulate decay of labile carbon, but over time as plant communities shift from fresh to polyhaline marsh, litter decay will decline, yielding greater potential for long-term carbon storage

A review of modelling the interaction between natural organic matter and metal cations

International Nuclear Information System (INIS)

Falck, W.E.

1989-01-01

This report reviews techniques available to model the interaction between natural organic matter (mainly fulvic and humic acids) and protons and metal cations. A concise definition of natural organic matter is given and their properties are outlined. These materials are macromolecules which exhibit a polyelectrolyte character owing to numerous dissociable functional groups which are attached to their carbon backbone or from integral parts of the structure. The polyelectrolyte character is thought to be responsible for their conformation, hydrogen bonding or bridging by metal cations between subunits being important mechanisms. Environmental parameters like pH and ionic strength thus will have profound effects on the conformation of natural organic matter, the properties of which can change from being a flexible polymer to being a rigid gel. Binding mechanisms and binding strengh are discussed and an overview of relevant techniques of investigation is given. This work is part of the Commission's Mirage project - Phase 2, research area Geochemistry of actinides and fission products in natural aquifer systems

Sources, fluxes, and behaviors of fluorescent dissolved organic matter (FDOM) in the Nakdong River Estuary, Korea

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Lee, Shin-Ah; Kim, Guebuem

2018-02-01

We monitored seasonal variations in dissolved organic carbon (DOC), the stable carbon isotope of DOC (δ13C-DOC), and fluorescent dissolved organic matter (FDOM) in water samples from a fixed station in the Nakdong River Estuary, Korea. Sampling was performed every hour during spring tide once a month from October 2014 to August 2015. The concentrations of DOC and humic-like FDOM showed significant negative correlations against salinity (r2 = 0.42-0.98, p ocean.

Interactions between iron and organic matter may influence the fate of permafrost carbon in the Arctic

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Cory, R. M.; Trusiak, A.; Ward, C.; Kling, G. W.; Tfaily, M.; Paša-Tolić, L.; Noel, V.; Bargar, J.

2017-12-01

The ongoing thawing of permafrost soils is the only environmental change that allows tremendous stores of organic carbon (C) to be converted into carbon dioxide (CO2) on decadal time scales, thus providing a positive and accelerating feedback to global warming. Evidence suggests that iron enhances abiotic reactions that convert dissolved organic matter (DOM) to CO2 in dark soils and in sunlit surface waters depending on its redox state and association with DOM (i.e., iron-DOM complexation). However, the complexation of iron in surface waters and soils remains too poorly understood to predict how iron influences the rates of oxidation of DOM to CO2. To address this knowledge gap, we characterized iron-DOM complexation in iron-rich soil and surface waters of the Arctic, in combination with measurements of DOM oxidation to CO2. These waters contain high concentrations of dissolved iron and DOM (up to 1 and 2 mM, respectively), and low concentrations of other potential ligands for iron such as sulfide, carbonate, chloride, or bromide. Ultra-high resolution mass spectrometry (FT-ICR MS) was used to identify ligands for iron within the DOM pool, and synchrotron based X-ray analysis (XAS and EXAFS) was used to assess iron's oxidation state, to detect iron complexation, and to constrain the chemical composition of the complexes. Across a natural gradient of dissolved iron and DOM concentrations, many potential ligands were identified within DOM that are expected to complex with iron (e.g., aromatic acids). EXAFS showed substantial complexation of reduced ferrous iron (Fe(II)) to DOM in arctic soil waters, on the basis of comparison to Fe(II)-DOM reference spectra. Identification of iron complexed to DOM in soil waters is consistent with strongly co-varying iron and DOM concentrations in arctic soil and surface waters, and supports our hypothesis that complexation of iron by DOM influences dark and light redox reactions that oxidize DOM to CO2. Understanding the molecular

Organic matter on Ceres: spectral analysis of the organic-rich area

Science.gov (United States)

Ammannito, E.; De Sanctis, M. C.; Vinogradoff, V.; Ciarniello, M.; Raponi, A.; Carrorro, F. G.; Raymond, C. A.; Russell, C. T.

2017-12-01

VIR, the Visible and InfraRed mapping spectrometer onboard the Dawn mission, has detected the presence of aliphatic carbons with the 3.3-3.5 µm bands, near the Ernutet crater [1]. The origin of this Organic Matter (OM) is likely related to an endogenous source but exogenic delivery cannot be excluded [1,2,6]. After the first identification of this organic rich (OR) area, mainly based on data taken by VIR [3] at a resolution of about 1 km/pixel, here we used VIR data obtained in the following orbital phases, at a resolution of about 400 m/pixel to analyze more closely the Ernutet organic-rich area. We investigated the possible correlation of the OM with other minerals present in the area. These observations can shed new light on the origin of such organic material. Different spectra with signatures of organics, corresponding to different areas around the Ernutet crater, have been extracted from the VIR data. We observed that several small areas are characterized by the presence of OM mixed with other species such as sodium carbonates and ammonium compounds. In particular, there is an area that shows a strong and large absorption at 3.07 µm along with a strong organic band at 3.4 µm and an enhanced carbonate band relative to the average Ceres background. Analyzing the absorption at 3.07 µm, we discovered that the band has several minima, with a strong minimum centered at 2.99-3.0 microns, other minima at 2.96, 3.11, 3.14-3.18 µm, as well as the usual minima at 3.07 µm. Several functional groups are active in the 2.9-3.2 µm region. CH, NH, and OH stretching modes indeed create absorptions at these wavelengths and identifying the molecules responsible for such features is not easy. Nevertheless, the presence of Na-carbonates, yet observed on other regions of Ceres (4,5) and the presence of these additional bands can reinforce the endogenic origin of the organics of Ceres. Their possible formation processes are described in a companion abstract (6). [1] De

Production and degradation of fluorescent dissolved organic matter in surface waters of the eastern north Atlantic ocean

NARCIS (Netherlands)

Lønborg, C.; Yokokawa, T.; Herndl, G.J.; Alvarez-Salgado, X.A.

2015-01-01

The distribution and fate of coloured dissolved organic matter (CDOM) in the epipelagic Eastern North Atlantic was investigated during a cruise in the summer 2009 by combining field observations and culture experiments. Dissolved organic carbon (DOC) and nitrogen (DON), the absorption spectra of

Soil Organic Carbon assessment on two different forest management

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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.

Evaluating Activated Carbon Adsorption of Dissolved Organic Matter and Micropollutants Using Fluorescence Spectroscopy.

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Shimabuku, Kyle K; Kennedy, Anthony M; Mulhern, Riley E; Summers, R Scott

2017-03-07

Dissolved organic matter (DOM) negatively impacts granular activated carbon (GAC) adsorption of micropollutants and is a disinfection byproduct precursor. DOM from surface waters, wastewater effluent, and 1 kDa size fractions were adsorbed by GAC and characterized using fluorescence spectroscopy, UV-absorption, and size exclusion chromatography (SEC). Fluorescing DOM was preferentially adsorbed relative to UV-absorbing DOM. Humic-like fluorescence (peaks A and C) was selectively adsorbed relative to polyphenol-like fluorescence (peaks T and B) potentially due to size exclusion effects. In the surface waters and size fractions, peak C was preferentially removed relative to peak A, whereas the reverse was found in wastewater effluent, indicating that humic-like fluorescence is associated with different compounds depending on DOM source. Based on specific UV-absorption (SUVA), aromatic DOM was preferentially adsorbed. The fluorescence index (FI), if interpreted as an indicator of aromaticity, indicated the opposite but exhibited a strong relationship with average molecular weight, suggesting that FI might be a better indicator of DOM size than aromaticity. The influence of DOM intermolecular interactions on adsorption were minimal based on SEC analysis. Fluorescence parameters captured the impact of DOM size on the fouling of 2-methylisoborneol and warfarin adsorption and correlated with direct competition and pore blockage indicators.

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

RECIPROCAL RELATIONSHIPS BETWEEN AGGREGATE STABILITY AND ORGANIC CARBON CHARACTERISTICS IN A FORESTED ECOSYSTEM OF NORTHERN NIGERIA

Directory of Open Access Journals (Sweden)

Halima Mohammed Lawal

2012-10-01

Full Text Available Soil organic matter associated with different size aggregates differ in structure and function; therefore, play different roles in soil organic carbon (SOC turnover. This study assessed the relationship between aggregate stability and soil organic carbon fractions in a forested soil. Aggregate stability characterized by mean weight diameter (MWD was correlated with the various pools of SOC in a regression model. Mean weight diameter presented a 46% influence on total organic carbon (TOC while, TOC accounts for 21.8% 0f aggregate stability. The unprotected and physically protected soil organic carbon did not significantly dictate stability of these soils. However, chemically protected and biochemically protected SOC influenced significantly aggregate stability of these forested soils.

Study of the trace metal ion influence on the turnover of soil organic matter in cultivated contaminated soils

International Nuclear Information System (INIS)

Dumat, C.; Quenea, K.; Bermond, A.; Toinen, S.; Benedetti, M.F.

2006-01-01

The role of metals in the behaviour of soil organic matter (SOM) is not well documented. Therefore, we investigated the influence of metals (Pb, Zn, Cu and Cd) on the dynamic of SOM in contaminated soils where maize (C 4 plant) replaced C 3 cultures. Three pseudogley brown leached soil profiles under maize with a decreasing gradient in metals concentrations were sampled. On size fractions, stable carbon isotopic ratio (δ 13 C), metals, organic carbon and nitrogen concentrations were measured in function of depth. The determined sequence for the amount of C 4 organic matter in the bulk fractions: M 3 (0.9) > M 2 (0.4) > M 1 (0.3) is in agreement with a significant influence of metals on the SOM turnover. New C 4 SOM, mainly present in the labile coarser fractions and less contaminated by metals than the stabilised C 3 SOM of the clay fraction, is more easily degraded by microorganisms. - Measure of δ 13 C and total metal concentrations in size fractions of contaminated soils suggests an influence of metals on the soil organic matter dynamic

Modeling Coupled Landscape Evolution and Soil Organic Carbon Dynamics in Intensively Management Landscapes

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Yan, Q.; Kumar, P.

2017-12-01

Soil is the largest reservoir of carbon in the biosphere but in agricultural areas it is going through rapid erosion due disturbance arising from crop harvest, tillage, and tile drainage. Identifying whether the production of soil organic carbon (SOC) from the crops can compensate for the loss due to erosion is critical to ensure our food security and adapt to climate change. In the U.S. Midwest where large areas of land are intensively managed for agriculture practices, predicting soil quantity and quality are critical for maintaining crop yield and other Critical Zone services. This work focuses on modeling the coupled landscape evolutions soil organic carbon dynamics in agricultural fields. It couples landscape evolution, surface water runoff, organic matter transformation, and soil moisture dynamics to understand organic carbon gain and loss due to natural forcing and farming practices, such as fertilizer application and tillage. A distinctive feature of the model is the coupling of surface ad subsurface processes that predicts both surficial changes and transport along with the vertical transport and dynamics. Our results show that landscape evolution and farming practices play dominant roles in soil organic carbon (SOC) dynamics both above- and below-ground. Contrary to the common assumption that a vertical profile of SOC concentration decreases exponentially with depth, we find that in many situations SOC concentration below-ground could be higher than that at the surface. Tillage plays a complex role in organic matter dynamics. On one hand, tillage would accelerate the erosion rate, on the other hand, it would improve carbon storage by burying surface SOC into below ground. Our model consistently reproduces the observed above- and below-ground patterns of SOC in the field sites of Intensively Managed Landscapes Critical Zone Observatory (IMLCZO). This model bridges the gaps between the landscape evolution, below- and above-ground hydrologic cycle, and

Effects of watershed history on dissolved organic matter characteristics in headwater streams

Science.gov (United States)

Youhei Yamashita; Brian D. Kloeppel; Jennifer Knoepp; Gregory L. Zausen; Rudolf Jaffe'

2011-01-01

Dissolved organic matter (DOM) is recognized as a major component in the global carbon cycle and is an important driver in aquatic ecosystem function. Climate, land use, and forest cover changes all impact stream DOM and alter biogeochemical cycles in terrestrial environments. We determined the temporal variation in DOM quantity and quality in headwater streams at a...

Determining Inorganic and Organic Carbon.

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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.