Compound-specific C- and H-isotope compositions of enclosed organic matter in carbonate rocks: Implications for source identification of sedimentary organic matter and paleoenvironmental reconstruction

Energy Technology Data Exchange (ETDEWEB)

Xiong Yongqiang [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China)], E-mail: xiongyq@gig.ac.cn; Wang Yanmei; Wang Yongquan; Xu Shiping [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China)

2007-11-15

The Bohai Bay Basin is one of the most important oil-producing provinces in China. Molecular organic geochemical characteristics of Lower Paleozoic source rocks in this area have been investigated by analyzing chemical and isotopic compositions of solvent extracts and acid-released organic matter from the Lower Paleozoic carbonate rocks in the Jiyang Sub-basin of the Bohai Bay Basin. The results indicate that enclosed organic matter in carbonate rocks has not been recognizably altered by post-depositional processes. Two end-member compositions are suggested for early organic matter trapped in the Lower Paleozoic carbonate rocks: (1) a source dominated by aquatic organisms and deposited in a relatively deep marine environment and (2) a relatively high saline, evaporative marine depositional environment. In contrast, chemical and isotopic compositions of solvent extracts from these Lower Paleozoic carbonate rocks are relatively complicated, not only inheriting original characteristics of their precursors, but also overprinted by various post-depositional alterations, such as thermal maturation, biodegradation and mixing. Therefore, the integration of both organic matter characteristics can provide more useful information on the origin of organic matter present in carbonate rocks and the environments of their deposition.

Molecular characterization of macrophyte-derived dissolved organic matters and their implications for lakes

Science.gov (United States)

Chemical properties of whole organic matter (OM) and its dissolved organic matter (DOM) fraction from six dominant macrophytes in Lake Dianchi were comparatively characterized, and their environmental implications were discussed. Significant differences in chemical composition of the OM samples were...

(Tropical) soil organic matter modelling: problems and prospects

NARCIS (Netherlands)

Keulen, van H.

2001-01-01

Soil organic matter plays an important role in many physical, chemical and biological processes. However, the quantitative relations between the mineral and organic components of the soil and the relations with the vegetation are poorly understood. In such situations, the use of models is an

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

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.

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.

A Novel Type of Oil—generating Organic Matter —Crystal—enclosed Organic Matter

Institute of Scientific and Technical Information of China (English)

周中毅; 裴存民; 等

1992-01-01

The comparative study of organic matter in carbonate rocks and argillaceous rocks from the same horizon indicates that the organic thermal maturities of carbonate rocks are much lower than those of argillaceous rocks .Ana extensive analysis of extracted and inclused organic matter from the same sample shows that inclused organic matter is different from extracted organic matter,and the thermal maturity of the former is usually lower than that of the latter in terms of biomarker structural parameters.It seems that carbonate mineras could preserve organic matter and retard organic maturation.The inclused organic matter,abundant in most carbonate rocks,will be released from minerals and transformed into oil and gas during the high-thermal maturity stage.

LOSS OF ORGANIC CHEMICALS IN SOIL: PURE COMPOUND TREATABILITY STUDIES

Science.gov (United States)

Comprehensive screening data on the treatability of 32 organic chemicals in soil were developed. Of the evaluated chemicals, 22 were phenolic compounds. Aerobic batch laboratory microcosm experiments were conducted using two soils: an acidic clay soil with <1% organic matter and ...

Chemical-Structural Changes of Organic Matter in a Semi-Arid Soil After Organic Amendment

Institute of Scientific and Technical Information of China (English)

C.NICOL(A)S; G.MASCIANDARO; T.HERN(A)NDEZ; C.GARCIA

2012-01-01

A 9-month incubation experiment using composted and non-composted amendments derived from vine pruning waste and sewage sludge was carried out to study the effects of the nature and stability of organic amendments on the structural composition of organic matter (OM) in a semi-arid soil. The changes of soil OM,both in the whole soil and in the extractable carbon with pyrophosphate,were evaluated by pyrolysis-gas chromatography and chemical analyses.By the end of the experiment,the soils amended with pruning waste exhibited less organic carbon loss than those receiving sewage sludge.The non-composted residues increased the aliphatic-pyrolytic products of the OM,both in the whole soil and also in the pyrophosphate extract,with the products derived from peptides and proteins being significantly higher.After 9 months,in the soils amended with pruning waste the relative abundance of phenolic-pyrolytic products derived from phenolic compounds,lignin and proteins in the whole soil tended to increase more than those in the soils amended with sewage sludge.However,the extractable OM with pyrophosphate in the soils amended with composted residues tended to have higher contents of these phenolic-pyrolytic products than that in non-composted ones.Thus,despite the stability of pruning waste,the composting of this material promoted the incorporation of phenolic compounds to the soil OM.The pyrolytic indices (furfural/pyrrole and aliphatic/aromatic ratios) showed the diminution of aliphatic compounds and the increase of aromatic compounds,indicating the stabilization of the OM in the amended soils after 9 months.In conclusion,the changes of soil OM depend on the nature and stability of the organic amendments,with composted vine pruning waste favouring humification.

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.

The energetic and chemical signatures of persistent soil organic matter

DEFF Research Database (Denmark)

Barré, Pierre; Plante, Alain F.; Cecillon, Lauric

2016-01-01

A large fraction of soil organic matter (OM) resists decomposition over decades to centuries as indicated by long radiocarbon residence times, but the mechanisms responsible for the long-term (multi-decadal) persistence are debated. The current lack of mechanistic understanding limits our ability...

Chemical Force Spectroscopy Evidence Supporting the Layer-by-Layer Model of Organic Matter Binding to Iron (oxy)Hydroxide Mineral Surfaces

KAUST Repository

Chassé , Alexander W.; Ohno, Tsutomu; Higgins, Steven R.; Amirbahman, Aria; Yildirim, Nadir; Parr, Thomas B.

2015-01-01

© 2015 American Chemical Society. The adsorption of dissolved organic matter (DOM) to metal (oxy)hydroxide mineral surfaces is a critical step for C sequestration in soils. Although equilibrium studies have described some of the factors controlling this process, the molecular-scale description of the adsorption process has been more limited. Chemical force spectroscopy revealed differing adhesion strengths of DOM extracted from three soils and a reference peat soil material to an iron (oxy)hydroxide mineral surface. The DOM was characterized using ultrahigh-resolution negative ion mode electrospray ionization Fourier Transform ion cyclotron resonance mass spectrometry. The results indicate that carboxyl-rich aromatic and N-containing aliphatic molecules of DOM are correlated with high adhesion forces. Increasing molecular mass was shown to decrease the adhesion force between the mineral surface and the DOM. Kendrick mass defect analysis suggests that mechanisms involving two carboxyl groups result in the most stable bond to the mineral surface. We conceptualize these results using a layer-by-layer "onion" model of organic matter stabilization on soil mineral surfaces.

Chemical Force Spectroscopy Evidence Supporting the Layer-by-Layer Model of Organic Matter Binding to Iron (oxy)Hydroxide Mineral Surfaces

KAUST Repository

Chassé, Alexander W.

2015-08-18

© 2015 American Chemical Society. The adsorption of dissolved organic matter (DOM) to metal (oxy)hydroxide mineral surfaces is a critical step for C sequestration in soils. Although equilibrium studies have described some of the factors controlling this process, the molecular-scale description of the adsorption process has been more limited. Chemical force spectroscopy revealed differing adhesion strengths of DOM extracted from three soils and a reference peat soil material to an iron (oxy)hydroxide mineral surface. The DOM was characterized using ultrahigh-resolution negative ion mode electrospray ionization Fourier Transform ion cyclotron resonance mass spectrometry. The results indicate that carboxyl-rich aromatic and N-containing aliphatic molecules of DOM are correlated with high adhesion forces. Increasing molecular mass was shown to decrease the adhesion force between the mineral surface and the DOM. Kendrick mass defect analysis suggests that mechanisms involving two carboxyl groups result in the most stable bond to the mineral surface. We conceptualize these results using a layer-by-layer "onion" model of organic matter stabilization on soil mineral surfaces.

Solid-state 13C NMR experiments reveal effects of aggregate size on the chemical composition of particulate organic matter in grazed steppe soils

Science.gov (United States)

Steffens, M.; Kölbl, A.; Kögel-Knabner, I.

2009-04-01

Grazing is one of the most important factors that may reduce soil organic matter (SOM) stocks and subsequently deteriorate aggregate stability in grassland topsoils. Land use management and grazing reduction are assumed to increase the input of OM, improve the soil aggregation and change species composition of vegetation (changes depth of OM input). Many studies have evaluated the impact of grazing cessation on SOM quantity. But until today little is known about the impact of grazing cessation on the chemical quality of SOM in density fractions, aggregate size classes and different horizons. The central aim of this study was to analyse the quality of SOM fractions in differently sized aggregates and horizons as affected by increased inputs of organic matter due to grazing exclusion. We applied a combined aggregate size, density and particle size fractionation procedure to sandy steppe topsoils with different organic matter inputs due to different grazing intensities (continuously grazed = Cg, winter grazing = Wg, ungrazed since 1999 = Ug99, ungrazed since 1979 = Ug79). Three different particulate organic matter (POM; free POM, in aggregate occluded POM and small in aggregate occluded POM) and seven mineral-associated organic matter fractions were separated for each of three aggregate size classes (coarse = 2000-6300 m, medium = 630-2000 m and fine =

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 ...

Chemical and biological characterization of urban particulate matter

International Nuclear Information System (INIS)

Agurell, E.; Alsberg, T.; Assefaz-Redda, Y.

1990-11-01

Airborne particulate matter has been collected on glass fiber filter by high volume sampling in the Goeteborg urban area. The samples were, after extraction with respect to organic components, tested for biological effect in the Salmonella mutagenicity assay, affinity to the cytosol TCDD receptor and toxicity towards a mammalian cell system and analysed chemically for selected polycyclic aromatic compounds. A series of samples collected simultaneously at a street level location and a rooftop site showed that most parameters associated with the organic compounds adsorbed to airborne particulate matter has similar concentrations at the two levels. The differences observed for the mutagenic effect in different strains and conditions showed that the rooftop samples had a different composition compared to the street samples indicating that atmospheric transformations have occurred. Chemical fractionation of representative samples showed that the distribution of mutagenic activity among different fractions is dissimilar to the distribution obtained in the fractionation of both gasoline and diesel engine exhaust particles. Partial least squares regression analysis showed qualitatively that diesel exhaust is a major source of airborne particulate mutagenic activity and source apportionment with chemical mass balance and multilinear regression corroborated this quantitatively. The multilinear regression analysis gave the result that the airborne activity in Salmonella TA90-S9 originated to 54±4% from diesel exhaust and to 26±3% from gasoline exhaust. The contribution is more equal for the activity measured with TA98+S9. The usefulness of short-term bioassays as an addition to chemical analysis of airborne particulate matter depends on whether only polycylic aromatic hydrocarbons (PAH) are major carcinogens, as has been suggested in the literature, or whether also other polycyclic aromatic compound (PAC) are of importance. (au)

Contribution to physico-chemical study of Timahdit bituminous schists (Morocco): Organic matters and metalloporphyrins

International Nuclear Information System (INIS)

Saoiabi, A.

1982-01-01

The Timahdit bituminous schists have been analysed by different methods. The experimental results obtained using these methods concern the behaviour of the schists and the Kerogen facing the pyrolysis, as well as the separation of the hydrocarbons and the metalloporphyrins. For this purpose the techniques used are: 'Rock Eval' pyrolysis, thermogravimetric analysis and electron paramagnetic resonance (E.P.R.) for the raw rock and the Kerogen; infrared (I.R.), gas chromatography and E.P.R. for the extracted organic matters; E.P.R., I.R., nuclear magnetic resonance (N.M.R.), ultraviolet (U.V.) and mass spectrometry for the metalloporphyrins identification and characterization. The analysis of these schists has shown that: We can extract per solvent only 1% of organic matters, ferric oxide hasn't any effect neither on the pyrolysis nor on the organic matters extraction and that the Kerogen of these schists are relatively rich in hydrocarbonic compounds. The gas chromatography reveal the presence of alkanes with odd number of carbons and isoprenoids. All these criteria indicate an immature, little developped organic matter which having probably a marine origin but possessing a good oil potential. It has also been observed that a part of Iron, Nickel and Vanadium in the schists are incorporated into the organic matters. Nickel and Vanadium are into macrocycles which are porphyrins. A method for extracting and separating these porphyrins has been developped. 43 figs., 21 tabs., 58 refs. (author)

Organic matters: investigating the sources, transport, and fate of organic matter in Fanno Creek, Oregon

Science.gov (United States)

Sobieszczyk, Steven; Keith, Mackenzie K.; Goldman, Jami H.; Rounds, Stewart A.

2015-01-01

The term organic matter refers to the remnants of all living material. This can include fallen leaves, yard waste, animal waste, downed timber, or the remains of any other plant and animal life. Organic matter is abundant both on land and in water. Investigating organic matter is necessary for understanding the fate and transport of carbon (a major constituent of organic matter).

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)

Chemical evaluation of soil organic matter structure in diverse cropping systems

Science.gov (United States)

Soil organic matter (SOM) improves soil structure, nutrient and water retention, and biodiversity while reducing susceptibility to soil erosion. SOM also represents an important pool of C that can be increased to help mitigate global climate change. Our understanding of how agricultural management ...

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

Science.gov (United States)

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

2002-12-01

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

Decomposition of soil organic matter from boreal black spruce forest: Environmental and chemical controls

Science.gov (United States)

Wickland, K.P.; Neff, J.C.

2008-01-01

Black spruce forests are a dominant covertype in the boreal forest region, and they inhabit landscapes that span a wide range of hydrologic and thermal conditions. These forests often have large stores of soil organic carbon. Recent increases in temperature at northern latitudes may be stimulating decomposition rates of this soil carbon. It is unclear, however, how changes in environmental conditions influence decomposition in these systems, and if substrate controls of decomposition vary with hydrologic and thermal regime. We addressed these issues by investigating the effects of temperature, moisture, and organic matter chemical characteristics on decomposition of fibric soil horizons from three black spruce forest sites. The sites varied in drainage and permafrost, and included a "Well Drained" site where permafrost was absent, and "Moderately well Drained" and "Poorly Drained" sites where permafrost was present at about 0.5 m depth. Samples collected from each site were incubated at five different moisture contents (2, 25, 50, 75, and 100% saturation) and two different temperatures (10??C and 20??C) in a full factorial design for two months. Organic matter chemistry was analyzed using pyrolysis gas chromatography-mass spectrometry prior to incubation, and after incubation on soils held at 20??C, 50% saturation. Mean cumulative mineralization, normalized to initial carbon content, ranged from 0.2% to 4.7%, and was dependent on temperature, moisture, and site. The effect of temperature on mineralization was significantly influenced by moisture content, as mineralization was greatest at 20??C and 50-75% saturation. While the relative effects of temperature and moisture were similar for all soils, mineralization rates were significantly greater for samples from the "Well Drained" site compared to the other sites. Variations in the relative abundances of polysaccharide-derivatives and compounds of undetermined source (such as toluene, phenol, 4-methyl phenol, and

Estimating pesticide sampling rates by the polar organic chemical integrative sampler (POCIS) in the presence of natural organic matter and varying hydrodynamic conditions

Science.gov (United States)

Charlestra, Lucner; Amirbahman, Aria; Courtemanch, David L.; Alvarez, David A.; Patterson, Howard

2012-01-01

The polar organic chemical integrative sampler (POCIS) was calibrated to monitor pesticides in water under controlled laboratory conditions. The effect of natural organic matter (NOM) on the sampling rates (Rs) was evaluated in microcosms containing -1 of total organic carbon (TOC). The effect of hydrodynamics was studied by comparing Rs values measured in stirred (SBE) and quiescent (QBE) batch experiments and a flow-through system (FTS). The level of NOM in the water used in these experiments had no effect on the magnitude of the pesticide sampling rates (p > 0.05). However, flow velocity and turbulence significantly increased the sampling rates of the pesticides in the FTS and SBE compared to the QBE (p < 0.001). The calibration data generated can be used to derive pesticide concentrations in water from POCIS deployed in stagnant and turbulent environmental systems without correction for NOM.

Comparison of the chemical composition of dissolved organic matter in three lakes in Minnesota

Science.gov (United States)

Cao, Xiaoyan; Aiken, George R.; Butler, Kenna D.; Mao, Jingdong; Schmidt-Rohr, Klaus

2018-01-01

New information on the chemical composition of dissolved organic matter (DOM) in three lakes in Minnesota has been gained from spectral editing and two-dimensional nuclear magnetic resonance (NMR) methods, indicating the effects of lake hydrological settings on DOM composition. Williams Lake (WL), Shingobee Lake (SL), and Manganika Lake (ML) had different source inputs, and the lake water residence time (WRT) of WL was markedly longer than that of SL and ML. The hydrophobic organic acid (HPOA) and transphilic organic acid (TPIA) fractions combined comprised >50% of total DOM in these lakes, and contained carboxyl-rich alicyclic molecules (CRAM), aromatics, carbohydrates, and N-containing compounds. The previously understudied TPIA fractions contained fewer aromatics, more oxygen-rich CRAM, and more N-containing compounds compared to the corresponding HPOA. CRAM represented the predominant component in DOM from all lakes studied, and more so in WL than in SL and ML. Aromatics including lignin residues and phenols decreased in relative abundances from ML to SL and WL. Carbohydrates and N-containing compounds were minor components in both HPOA and TPIA and did not show large variations among the three lakes. The increased relative abundances of CRAM in DOM from ML, SL to WL suggested the selective preservation of CRAM with increased residence time.

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

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.

CHEMICAL CLEANING OF NANOFILTRATION MEMBRANES FOULED BY ORGANIC MATTERS

Directory of Open Access Journals (Sweden)

CHARLENE C. H. KOO

2016-07-01

Full Text Available Membrane fouling is a term to describe non-integral substance on membrane surface which results in rapid decline of permeation flux and deteriorate the performance of membrane. Chemical cleaning agents especially like alkaline cleaners are most widely employed to restore the membrane performance. This research mainly investigated the potential use of sodium hydroxide (NaOH and sodium hypochlorite (NaOCl as the chemical cleaning agents to restore the permeate flux of organically fouled nanofiltration (NF membranes under varying applied pressure and flow condition. The performances of the cleaning protocols were quantified using flux recovery and resistance removal. The results demonstrated that NaOCl is more effective than NaOH. This observation is also in line with FTIR analysis in which the transmittance intensity showed by FTIR spectra of NaOCl is higher than that of NaOH. The results also reported that higher flux recovery and resistance removal were achieved when the fouled NF membranes were cleaned with higher concentration of chemical agents and applied pressure. However, the improvements of flux recovery and resistance removal by increasing the applied pressure were found insignificant at higher applied pressure range (16 to 18 bar than the lower applied pressure range (i.e. 12 to 14 bar. This research plays an important role by identifying the key parameters that could restore the flux of organically fouled NF membranes significantly.

Chemical and isotopic signature of bulk organic matter and hydrocarbon biomarkers within mid-slope accretionary sediments of the northern Cascadia margin gas hydrate system

Science.gov (United States)

Kaneko, Masanori; Shingai, Hiroshi; Pohlman, John W.; Naraoka, Hiroshi

2010-01-01

The chemical and isotopic compositions of sedimentary organic matter (SOM) from two mid-slope sites of the northern Cascadia margin were investigated during Integrated Ocean Drilling Program (IODP) Expedition 311 to elucidate the organic matter origins and identify potential microbial contributions to SOM. Gas hydrate is present at both locations (IODP Sites U1327 and U1328), with distinct patterns of near-seafloor structural accumulations at the cold seep Site U1328 and deeper stratigraphic accumulations at the slope-basin Site U1327. Source characterization and evidence that some components of the organic matter have been diagenetically altered are determined from the concentrations and isotopic compositions of hydrocarbon biomarkers, total organic carbon (TOC), total nitrogen (TN) and total sulfur (TS). The carbon isotopic compositions of TOC (δ13CTOC = −26 to −22‰) and long-chain n-alkanes (C27, C29 and C31, δ13C = −34 to − 29‰) suggest the organic matter at both sites is a mixture of 1) terrestrial plants that employ the C3 photosynthetic pathway and 2) marine algae. In contrast, the δ15NTN values of the bulk sediment (+ 4 to + 8‰) are consistent with a predominantly marine source, but these values most likely have been modified during microbial organic matter degradation. The δ13C values of archaeal biomarker pentamethylicosane (PMI) (− 46.4‰) and bacterial-sourced hopenes, diploptene and hop-21-ene (− 40.9 to − 34.7‰) indicate a partial contribution from methane carbon or a chemoautotrophic pathway. Our multi-isotope and biomarker-based conclusions are consistent with previous studies, based only on the elemental composition of bulk sediments, that suggested a mixed marine-terrestrial organic matter origin for these mid-slope sites of the northern Cascadia margin.

Influence of chemical and structural evolution of dissolved organic matter on electron transfer capacity during composting

International Nuclear Information System (INIS)

He, Xiao-Song; Xi, Bei-Dou; Cui, Dong-Yu; Liu, Yong; Tan, Wen-Bin; Pan, Hong-Wei; Li, Dan

2014-01-01

Highlights: • Electron transfer capability (ETC) of compost-derived DOM was investigated. • Composting treatment increased the ETC of DOM from municipal solid wastes. • The ETC increase related to humic matter, and molecule weight, and N and S content. - Abstract: Dissolved organic matter (DOM) can mediate electron transfer and change chemical speciation of heavy metals. In this study, the electron transfer capability (ETC) of compost-derived DOM was investigated through electrochemical approaches, and the factors influencing the ETC were studied using spectral and elemental analysis. The results showed that the electron accepting capacity (EAC) and electron donating capacity (EDC) of compost-derived DOM were 3.29–40.14 μmol e− (g C) −1 and 57.1– 346.07 μmol e− (g C) −1 , respectively. Composting treatment increased the fulvic- and humic-like substance content, oxygenated aliphatic carbon content, lignin-derived aromatic carbon content, molecule weight, and N and S content of DOM, but decreased the aliphatic carbon content and the C and H content. This conversion increased the EDC and EAC of the DOM during composting

Aqueous organic chemistry in the atmosphere: sources and chemical processing of organic aerosols.

Science.gov (United States)

McNeill, V Faye

2015-02-03

Over the past decade, it has become clear that aqueous chemical processes occurring in cloud droplets and wet atmospheric particles are an important source of organic atmospheric particulate matter. Reactions of water-soluble volatile (or semivolatile) organic gases (VOCs or SVOCs) in these aqueous media lead to the formation of highly oxidized organic particulate matter (secondary organic aerosol; SOA) and key tracer species, such as organosulfates. These processes are often driven by a combination of anthropogenic and biogenic emissions, and therefore their accurate representation in models is important for effective air quality management. Despite considerable progress, mechanistic understanding of some key aqueous processes is still lacking, and these pathways are incompletely represented in 3D atmospheric chemistry and air quality models. In this article, the concepts, historical context, and current state of the science of aqueous pathways of SOA formation are discussed.

In Situ Mapping of the Organic Matter in Carbonaceous Chondrites and Mineral Relationships

Science.gov (United States)

Clemett, Simon J.; Messenger, S.; Thomas-Keprta, K. L.; Ross, D. K.

2012-01-01

Carbonaceous chondrite organic matter represents a fossil record of reactions that occurred in a range of physically, spatially and temporally distinct environments, from the interstellar medium to asteroid parent bodies. While bulk chemical analysis has provided a detailed view of the nature and diversity of this organic matter, almost nothing is known about its spatial distribution and mineralogical relationships. Such information is nevertheless critical to deciphering its formation processes and evolutionary history.

Chemical characterization of organic particulate matter from on-road traffic in São Paulo, Brazil

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B. S. Oyama

2016-11-01

Full Text Available This study reports emission of organic particulate matter by light-duty vehicles (LDVs and heavy-duty vehicles (HDVs in the city of São Paulo, Brazil, where vehicles run on three different fuel types: gasoline with 25 % ethanol (called gasohol, E25, hydrated ethanol (E100, and diesel (with 5 % biodiesel. The experiments were performed at two tunnels: Jânio Quadros (TJQ, where 99 % of the vehicles are LDVs, and RodoAnel Mário Covas (TRA, where up to 30 % of the fleet are HDVs. Fine particulate matter (PM2.5 samples were collected on quartz filters in May and July 2011 at TJQ and TRA, respectively. The samples were analyzed by thermal-desorption proton-transfer-reaction mass spectrometry (TD-PTR-MS and by thermal–optical transmittance (TOT. Emission factors (EFs for organic aerosol (OA and organic carbon (OC were calculated for the HDV and the LDV fleet. We found that HDVs emitted more PM2.5 than LDVs, with OC EFs of 108 and 523 mg kg−1 burned fuel for LDVs and HDVs, respectively. More than 700 ions were identified by TD-PTR-MS and the EF profiles obtained from HDVs and LDVs exhibited distinct features. Unique organic tracers for gasoline, biodiesel, and tire wear have been tentatively identified. nitrogen-containing compounds contributed around 20 % to the EF values for both types of vehicles, possibly associated with incomplete fuel burning or fast secondary production. Additionally, 70 and 65 % of the emitted mass (i.e. the OA originates from oxygenated compounds from LDVs and HDVs, respectively. This may be a consequence of the high oxygen content of the fuel. On the other hand, additional oxygenation may occur during fuel combustion. The high fractions of nitrogen- and oxygen-containing compounds show that chemical processing close to the engine / tailpipe region is an important factor influencing primary OA emission. The thermal-desorption analysis showed that HDVs emitted compounds with higher volatility, and with

Using thermal analysis to evaluate the fire effects on organic matter content of Andisols

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J. Neris

2013-09-01

Full Text Available Soil organic compounds play a relevant role in aggregate stability and thus, in the susceptibility of soils to erosion. Thermal analysis (N2 and air and chemical oxidation techniques (dichromate and permanganate oxidation were used to evaluate the effects of a forest fire on the organic matter of Andisols. Both thermal analysis and chemical methods showed a decrease in the organic matter content and an increase in the recalcitrance of the remaining organic compounds in the burned zones. Thermal analysis indicated an increase in the thermal stability of the organic compounds of fire-affected soils and a lower content of both labile and recalcitrant pools as a consequence of the fire. However, this decrease was relatively higher in the labile pool and lower in the recalcitrant one, indicative of an increase in the recalcitrance of the remaining organic compounds. Apparently, black carbon did not burn under our experimental conditions. Under N2, the results showed a lower labile and a higher recalcitrant and refractory contents in burned and some unburned soils, possibly due to the lower decomposition rate under N2 flux. Thermal analysis using O2 and the chemical techniques showed a positive relation, but noticeable differences in the total amount of the labile pool. Thermal analysis methods provide direct quantitative information useful to characterize the soil organic matter quality and to evaluate the effects of fire on soils.

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)

The Effect of paper mill waste and sewage sludge amendments on soil organic matter

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Méndez, Ana; Barriga, Sandra; Guerrero, Francisca; Gascó, Gabriel

2013-04-01

In general, Mediterranean soils have low organic matter content, due to the climate characteristics of this region and inadequate land management. Traditionally, organic wastes such as manure are used as amendment in order to improve the soil quality, increasing soil fertility by the accumulation of nitrogen, phosphorus and other plant nutrients in the soil. In the last decade, other anthropogenic organic wastes such as sewage sludge or paper waste materials have been studied as soil amendments to improve physical, chemical and biological properties of soils. The objective of the present work was to study the influence of waste from a paper mill and sewage sludge amendments on soil organic matter. For this reason, soil organic matter evolution was studied using thermogravimetric analysis (TGA), the derivative (dTG) and differential thermal analysis (DTA). Thermal analytical techniques have the advantage of using full samples without pre-treatments and have been extensively used to study the evolution of organic matter in soils, to evaluate composting process or to study the evolution of organic matter of growing media.

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.

Organic matter loading affects lodgepole pine seedling growth.

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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.

Iron oxides and quality of organic matter in sugarcane harvesting systems

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Diogo Mazza Barbieri

2014-08-01

Full Text Available Improvements in working conditions, sustainable production, and competitiveness have led to substantial changes in sugarcane harvesting systems. Such changes have altered a number of soil properties, including iron oxides and organic matter, as well as some chemical properties, such as the maximum P adsorption capacity of the soil. The aim of this study was to characterize the relationship between iron oxides and the quality of organic matter in sugarcane harvesting systems. For that purpose, two 1 ha plots in mechanically and manually harvested fields were used to obtain soil samples from the 0.00-0.25 m soil layer at 126 different points. The mineralogical, chemical, and physical results were subjected to descriptive statistical analyses, such as the mean comparison test, as well as to multivariate statistical and principal component analyses. Multivariate tests allowed soil properties to be classified in two different groups according to the harvesting method: manual harvest with the burning of residual cane, and mechanical harvest without burning. The mechanical harvesting system was found to enhance pedoenvironmental conditions, leading to changes in the crystallinity of iron oxides, an increase in the humification of organic matter, and a relative decrease in phosphorus adsorption in this area compared to the manual harvesting system.

Composition of structural fragments and the mineralization rate of organic matter in zonal soils

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Larionova, A. A.; Zolotareva, B. N.; Kolyagin, Yu. G.; Kvitkina, A. K.; Kaganov, V. V.; Kudeyarov, V. N.

2015-10-01

Comparative analysis of the climatic characteristics and the recalcitrance against decomposition of organic matter in the zonal soil series of European Russia, from peat surface-gley tundra soil to brown semidesert soil, has assessed the relationships between the period of biological activity, the content of chemically stable functional groups, and the mineralization of humus. The stability of organic matter has been determined from the ratio of functional groups using the solid-state 13C NMR spectroscopy of soil samples and the direct measurements of organic matter mineralization from CO2 emission. A statistically significant correlation has been found between the period of biological activity and the humification indices: the CHA/CFA ratio, the aromaticity, and the alkyl/ O-alkyl ratio in organic matter. The closest correlation has been observed between the period of biological activity and the alkyl/ O-alkyl ratio; therefore, this parameter can be an important indicator of the soil humus status. A poor correlation between the mineralization rate and the content of chemically stable functional groups in soil organic matter has been revealed for the studied soil series. At the same time, the lowest rate of carbon mineralization has been observed in southern chernozem characterized by the maximum content of aromatic groups (21% Corg) and surface-gley peat tundra soil, where an extremely high content of unsubstituted CH2 and CH3 alkyl groups (41% Corg) has been noted.

Changes in the chemical characteristics of water-extracted organic matter from vermicomposting of sewage sludge and cow dung.

Science.gov (United States)

Xing, Meiyan; Li, Xiaowei; Yang, Jian; Huang, Zhidong; Lu, Yongsen

2012-02-29

The chemical changes of water-extractable organic matter (WEOM) from five different substrates of sewage sludge enriched with different proportions of cow dung after vermicomposting with Eisenia fetida were investigated using various analytical approaches. Results showed that dissolved organic carbon, chemical oxygen demand, and C/N ratio of the substrates decreased significantly after vermicomposting process. The aromaticity of WEOM from the substrates enhanced considerably, and the amount of volatile fatty acids declined markedly, especially for the cow dung substrate. Gel filtration chromatography analysis showed that the molecular weight fraction between 10(3) and 10(6) Da became the main part of WEOM in the final product. 1H nuclear magnetic resonance spectra revealed that the proportion of H moieties in the area of 0.00-3.00 ppm decreased, while increasing at 3.00-4.25 ppm after vermicomposting. Fluorescence spectra indicated that vermicomposting caused the degradation of protein-like groups, and the formation of fulvic and humic acid-like compounds in the WEOM of the substrates. Overall results indicate clearly that vermicomposting promoted the degradation and transformation of liable WEOM into biological stable substances in sewage sludge and cow dung alone, as well as in mixtures of both materials, and testing the WEOM might be an effective way to evaluate the biological maturity and chemical stability of vermicompost. Copyright © 2011 Elsevier B.V. All rights reserved.

Influence of chemical and structural evolution of dissolved organic matter on electron transfer capacity during composting

Energy Technology Data Exchange (ETDEWEB)

He, Xiao-Song [State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012 (China); Innovation base of Ground Water and Environmental System Engineering, Chinese Research Academy of Environmental Science, Beijing 100012 (China); Xi, Bei-Dou, E-mail: hexs82@126.com [State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012 (China); Innovation base of Ground Water and Environmental System Engineering, Chinese Research Academy of Environmental Science, Beijing 100012 (China); Cui, Dong-Yu [State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012 (China); Innovation base of Ground Water and Environmental System Engineering, Chinese Research Academy of Environmental Science, Beijing 100012 (China); Liu, Yong [Guangdong Key Laboratory of Agro-Environmental Integrated Control, Guangdong Institute of Eco-Environmental and Soil Sciences, Guangzhou 510650 (China); Tan, Wen-Bin; Pan, Hong-Wei; Li, Dan [State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012 (China); Innovation base of Ground Water and Environmental System Engineering, Chinese Research Academy of Environmental Science, Beijing 100012 (China)

2014-03-01

Highlights: • Electron transfer capability (ETC) of compost-derived DOM was investigated. • Composting treatment increased the ETC of DOM from municipal solid wastes. • The ETC increase related to humic matter, and molecule weight, and N and S content. - Abstract: Dissolved organic matter (DOM) can mediate electron transfer and change chemical speciation of heavy metals. In this study, the electron transfer capability (ETC) of compost-derived DOM was investigated through electrochemical approaches, and the factors influencing the ETC were studied using spectral and elemental analysis. The results showed that the electron accepting capacity (EAC) and electron donating capacity (EDC) of compost-derived DOM were 3.29–40.14 μmol{sub e−} (g C){sup −1} and 57.1– 346.07 μmol{sub e−} (g C){sup −1}, respectively. Composting treatment increased the fulvic- and humic-like substance content, oxygenated aliphatic carbon content, lignin-derived aromatic carbon content, molecule weight, and N and S content of DOM, but decreased the aliphatic carbon content and the C and H content. This conversion increased the EDC and EAC of the DOM during composting.

Linking measurements of biodegradability, thermal stability and chemical composition to evaluate the effects of management on soil organic matter

Science.gov (United States)

Gregorich, Ed; Gillespie, Adam; Beare, Mike; Curtin, Denis; Sanei, Hamed; Yanni, Sandra

2015-04-01

The stability of soil organic matter (SOM) as it relates to resistance to microbial degradation has important implications for nutrient cycling, emission of greenhouse gases, and C sequestration. Hence, there is interest in developing new ways to accurately quantify and characterise the labile and stable forms of soil organic C. Our objectives in this study were to evaluate and describe relationships among the biodegradability, thermal stability and chemistry of SOM in soil under widely contrasting management regimes. Samples from the same soil under permanent pasture, an arable cropping rotation, and chemical fallow were fractionated (sand: 2000-50 μm; silt: 50-5 μm, and clay: managements and that sand-associated organic matter was significantly more susceptible than that in the silt or clay fractions. Analysis by XANES showed accumulation of carboxylates and strong depletion of amides (protein) and aromatics in the fallow whole soil. Moreover, protein depletion was most significant in the sand fraction of the fallow soil. Sand fractions in fallow and cropped soils were, however, enriched in plant-derived phenols, aromatics and carboxylates compared to the sand fraction of pasture soils. In contrast, ketones, which have been identified as products of microbially-processed organic matter, were slightly enriched in the silt fraction of the pasture soil. These data suggest reduced inputs and cropping restrict the decomposition of plant residues and, without supplemental N additions, protein-N in native SOM is significantly mineralized in fallow systems to meet microbial C mineralization demands. Analytical pyrolysis showed distinct differences in the thermal stability of SOM among the size fractions and management treatments; it also showed that the loss of SOM generally involved dehydrogenation. The temperature at which half of the C was pyrolyzed showed strong correlation with mineralizable C and thus provides solid evidence for a link between the biological and

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 ...

Insights into the nature of cometary organic matter from terrestrial analogues

Science.gov (United States)

Court, Richard W.; Sephton, Mark A.

2012-04-01

The nature of cometary organic matter is of great interest to investigations involving the formation and distribution of organic matter relevant to the origin of life. We have used pyrolysis-Fourier transform infrared (FTIR) spectroscopy to investigate the chemical effects of the irradiation of naturally occurring bitumens, and to relate their products of pyrolysis to their parent assemblages. The information acquired has then been applied to the complex organic matter present in cometary nuclei and comae. Amalgamating the FTIR data presented here with data from published studies enables the inference of other comprehensive trends within hydrocarbon mixtures as they are progressively irradiated in a cometary environment, namely the polymerization of lower molecular weight compounds; an increased abundance of polycyclic aromatic hydrocarbon structures; enrichment in 13C; reduction in atomic H/C ratio; elevation of atomic O/C ratio and increase in the temperature required for thermal degradation. The dark carbonaceous surface of a cometary nucleus will display extreme levels of these features, relative to the nucleus interior, while material in the coma will reflect the degree of irradiation experienced by its source location in the nucleus. Cometary comae with high methane/water ratios indicate a nucleus enriched in methane, favouring the formation of complex organic matter via radiation-induced polymerization of simple precursors. In contrast, production of complex organic matter is hindered in a nucleus possessing a low methane/water ration, with the complex organic matter that does form possessing more oxygen-containing species, such as alcohol, carbonyl and carboxylic acid functional groups, resulting from reactions with hydroxyl radicals formed by the radiolysis of the more abundant water. These insights into the properties of complex cometary organic matter should be of particular interest to both remote observation and space missions involving in situ

Characteristics and Biodegradability of Wastewater Organic Matter in Municipal Wastewater Treatment Plants Collecting Domestic Wastewater and Industrial Discharge

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Yun-Young Choi

2017-06-01

Full Text Available Municipal wastewater treatment plants (WWTPs in Korea collect and treat not only domestic wastewater, but also discharge from industrial complexes. However, some industrial discharges contain a large amount of non-biodegradable organic matter, which cannot be treated properly in a conventional biological WWTP. This study aimed to investigate the characteristics and biodegradability of the wastewater organic matter contained in the industrial discharges and to examine the fate of the industrial discharges in a biological WWTP. In contrast to most previous studies targeting a specific group of organic compounds or traditional water quality indices, such as biological oxygen demand (BOD and chemical oxygen demand (COD, this study was purposed to quantify and characterize the biodegradable and nonbiodegradable fractions of the wastewater organic matter. Chemical oxygen demand (COD fractionation tests and fluorescence spectroscopy revealed that the industrial discharge from dyeing or pulp mill factories contained more non-biodegradable soluble organic matter than did the domestic wastewater. Statistical analysis on the WWTPs’ monitoring data indicated that the industrial discharge containing non-biodegradable soluble organic matter was not treated effectively in a biological WWTP, but was escaping from the system. Thus, industrial discharge that contained non-biodegradable soluble organic matter was a major factor in the decrease in biodegradability of the discharge, affecting the ultimate fate of wastewater organic matter in a biological WWTP. Further application of COD fractionation and fluorescence spectroscopy to wastewaters, with various industrial discharges, will help scientists and engineers to better design and operate a biological WWTP, by understanding the fate of wastewater organic matter.

Quantifying the degradation of organic matter in marine sediments: A review and synthesis

Science.gov (United States)

Arndt, Sandra; Jørgensen, B. B.; LaRowe, D. E.; Middelburg, J. J.; Pancost, R. D.; Regnier, P.

2013-08-01

Quantifying the rates of biogeochemical processes in marine sediments is essential for understanding global element cycles and climate change. Because organic matter degradation is the engine behind benthic dynamics, deciphering the impact that various forces have on this process is central to determining the evolution of the Earth system. Therefore, recent developments in the quantitative modeling of organic matter degradation in marine sediments are critically reviewed. The first part of the review synthesizes the main chemical, biological and physical factors that control organic matter degradation in sediments while the second part provides a general review of the mathematical formulations used to model these processes and the third part evaluates their application over different spatial and temporal scales. Key transport mechanisms in sedimentary environments are summarized and the mathematical formulation of the organic matter degradation rate law is described in detail. The roles of enzyme kinetics, bioenergetics, temperature and biomass growth in particular are highlighted. Alternative model approaches that quantify the degradation rate constant are also critically compared. In the third part of the review, the capability of different model approaches to extrapolate organic matter degradation rates over a broad range of temporal and spatial scales is assessed. In addition, the structure, functions and parameterization of more than 250 published models of organic matter degradation in marine sediments are analyzed. The large range of published model parameters illustrates the complex nature of organic matter dynamics, and, thus, the limited transferability of these parameters from one site to another. Compiled model parameters do not reveal a statistically significant correlation with single environmental characteristics such as water depth, deposition rate or organic matter flux. The lack of a generic framework that allows for model parameters to be

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.

NMR studies of chemical structural variation of insoluble organic matter from different carbonaceous chondrite groups

Science.gov (United States)

Cody, George D.; Alexander, Conel M. O.'D.

2005-02-01

Solid-state 1H and 13C Nuclear Magnetic Resonance (NMR) spectroscopic experiments have been performed on isolated meteoritic Insoluble Organic Matter (IOM) spanning four different carbonaceous chondrite meteorite groups; a CR2 (EET92042), a CI1 (Orgueil), a CM2 (Murchison), and the unique C2 meteorite, Tagish Lake. These solid state NMR experiments reveal considerable variation in bulk organic composition across the different meteorite group's IOM. The fraction of aromatic carbon increases as CR2 meteorite groups. Single pulse (SP) 13C magic angle spinning (MAS) NMR experiments reveal the presence of nanodiamonds with an apparent concentration ranking in the IOM of CR2 IOM of all four meteoritic IOM fractions are highly substituted. Fast spinning SP 1H MAS NMR spectral data combined with other NMR experimental data reveal that the average hydrogen content of sp 3 bonded carbon functional groups is low, requiring a high degree of aliphatic chain branching in each IOM fraction. The variation in chemistry across the meteorite groups is consistent with alteration by low temperature chemical oxidation. It is concluded that such chemistry principally affected the aliphatic moieties whereas the aromatic moieties and nanodiamonds may have been largely unaffected.

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

A GCM study of organic matter in marine aerosol and its potential contribution to cloud drop activation

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G. J. Roelofs

2008-02-01

Full Text Available With the global aerosol-climate model ECHAM5-HAM we investigate the potential influence of organic aerosol originating from the ocean on aerosol mass and chemical composition and the droplet concentration and size of marine clouds. We present sensitivity simulations in which the uptake of organic matter in the marine aerosol is prescribed for each aerosol mode with varying organic mass and mixing state, and with a geographical distribution and seasonality similar to the oceanic emission of dimethyl sulfide. Measurements of aerosol mass, aerosol chemical composition and cloud drop effective radius are used to assess the representativity of the model initializations. Good agreement with the measurements is obtained when organic matter is added to the Aitken, accumulation and coarse modes simultaneously. Representing marine organics in the model leads to higher cloud drop number concentrations and thus smaller cloud drop effective radii, and this improves the agreement with measurements. The mixing state of the organics and the other aerosol matter, i.e. internal or external depending on the formation process of aerosol organics, is an important factor for this. We estimate that globally about 75 Tg C yr⁻¹ of organic matter from marine origin enters the aerosol phase, with comparable contributions from primary emissions and secondary organic aerosol formation.

Physical and chemical evolution of reduced organic matter in the ISM

Science.gov (United States)

Jenniskens, Peter; Blake, David F.

1995-01-01

Icy mantles on interstellar grains have been a topic of study in airborne astronomy. Recent laboratory analog studies of the yield of organic residue from UV photolyzed ices have shown that this mechanism can be the most significant source of complex reduced organic matter in the interstellar medium. However, the total yield is a function of the occurrence of heating events that evaporate the ice, i.e. T is greater than 130 K, and the mechanism for such events is debated. Recently, we proposed that the recombination of radicals in the ice does not need high temperature excursions and, instead, occurs during a structural transformation of water ice at temperatures in the range 38 - 68 K.

Sorption of polycyclic aromatic hydrocarbons on particulate organic matters

International Nuclear Information System (INIS)

Guo Xueyan; Luo Lei; Ma Yibing; Zhang Shuzhen

2010-01-01

Particulate organic matter (POM) is a key organic matter fraction which can influence soil fertility. Its interactions with hydrophobic organic pollutants (HOCs) have not been characterized and the mechanisms of retention of HOCs by POM remain unclear. In the present study, sorption behaviors of polycyclic aromatic hydrocarbons (PAHs) naphthalene (NAP), phenanthrene (PHE), and pyrene (PYR) by POMs separated from different soils were examined and the POMs were characterized by elemental analysis, solid state 13 C NMR, and Fourier transform infrared spectroscopy (FT-IR). The results indicated that POMs were mainly composed of aliphatic components with high polarity. The different original POMs showed similar chemical composition and configuration. Sorption behaviors of PAHs indicated that there was no significant difference in sorption capacity among the POMs. Sorption of NAP and PHE by POMs displayed a nonlinear isotherm, while sorption of PYR yielded a linear isotherm. No significant hysteresis and ionic strength effect were observed for PAH desorption from the POMs.

Chemical Composition of Fine Particulate Matter and Life Expectancy

Science.gov (United States)

Dominici, Francesca; Wang, Yun; Correia, Andrew W.; Ezzati, Majid; Pope, C. Arden; Dockery, Douglas W.

2016-01-01

Background In a previous study, we provided evidence that a decline in fine particulate matter (PM2.5) air pollution during the period between 2000 and 2007 was associated with increased life expectancy in 545 counties in the United States. In this article, we investigated which chemical constituents of PM2.5 were the main drivers of the observed association. Methods We estimated associations between temporal changes in seven major components of PM2.5 (ammonium, sulfate, nitrate, elemental carbon matter, organic carbon matter, sodium, and silicon) and temporal changes in life expectancy in 95 counties between 2002 and 2007. We included US counties that had adequate chemical components of PM2.5 mass data across all seasons. We fitted single pollutant and multiple pollutant linear models, controlling for available socioeconomic, demographic, and smoking variables and stratifying by urban and nonurban counties. Results In multiple pollutant models, we found that: (1) a reduction in sulfate was associated with an increase in life expectancy; and (2) reductions in ammonium and sodium ion were associated with increases in life expectancy in nonurban counties only. Conclusions Our findings suggest that recent reductions in long-term exposure to sulfate, ammonium, and sodium ion between 2002 and 2007 are associated with improved public health. PMID:25906366

Evolution of organic matter in Orgueil, Murchison and Renazzo during parent body aqueous alteration: In situ investigations

Science.gov (United States)

Le Guillou, Corentin; Bernard, Sylvain; Brearley, Adrian J.; Remusat, Laurent

2014-04-01

Chondrites accreted the oldest solid materials in the solar system including dust processed in the protoplanetary disk and diverse organic compounds. After accretion, asteroidal alteration may have impacted organic particles in various ways. To constrain these processes, we conducted a comprehensive study of organics disseminated within the matrices of the three carbonaceous chondrite falls, Renazzo (CR2), Murchison (CM2) and Orgueil (CI). By combining synchrotron-based STXM and TEM analyses on FIB sections of samples previously characterized by NanoSIMS, we investigated the influence of aqueous alteration on the morphology, isotopic signature, molecular structure, spatial distribution, and mineralogical environment of the organic matter within the matrices. Two different populations of materials are distinguishable: sub-micrometric individual grains, likely dominated by insoluble compounds and diffuse organic matter, finely interspersed within phyllosilicates and/or (amorphous) nanocarbonates at the nanometer scale. We suggest that this latter component, which is depleted in aromatics and enriched in carboxylic functional groups, may be dominated by soluble compounds. Organic matter in Renazzo (CR) mainly consists of chemically-homogeneous individual grains surrounded by amorphous and nanocrystalline phyllosilicates. Evidence of connectivity between organic grains and fractures indicates that redistribution has occurred: some areas containing diffuse organic matter can be observed. This diffuse organic component is more abundant in Murchison (CM) and Orgueil (CI). This is interpreted as resulting from fluid transport at the micrometer scale and encapsulation within recrystallized alteration phases. In contrast to Renazzo, organic grains in Murchison and Orgueil display strong chemical heterogeneities, likely related to chemical evolution during aqueous alteration. The observations suggest that the altering fluid was a brine with elevated concentrations of both

Chemical and optical changes in freshwater dissolved organic matter exposed to solar radiation

Science.gov (United States)

Osburn, C.L.; Morris, D.P.; Thorn, K.A.; Moeller, R.E.

2001-01-01

We studied the chemical and optical changes in the dissolved organic matter (DOM) from two freshwater lakes and a Sphagnum bog after exposure to solar radiation. Stable carbon isotopes and solid-state 13C-NMR spectra of DOM were used together with optical and chemical data to interpret results from experimental exposures of DOM to sunlight and from seasonal observations of two lakes in northeastern Pennsylvania. Solar photochemical oxidation of humic-rich bog DOM to smaller LMW compounds and to DIC was inferred from losses of UV absorbance, optical indices of molecular weight and changes in DOM chemistry. Experimentally, we observed a 1.2??? enrichment in ??13C and a 47% loss in aromatic C functionality in bog DOM samples exposed to solar UVR. Similar results were observed in the surface waters of both lakes. In late summer hypolimnetic water in humic Lake Lacawac, we observed 3 to 4.5??? enrichments in ??13C and a 30% increase in aromatic C relative to early spring values during spring mixing. These changes coincided with increases in molecular weight and UV absorbance. Anaerobic conditions of the hypolimnion in Lake Lacawac suggest that microbial metabolism may be turning over allochthonous C introduced during spring mixing, as well as autochthonous C. This metabolic activity produces HMW DOM during the summer, which is photochemically labile and isotopically distinct from allochthonous DOM or autochthonous DOM. These results suggest both photooxidation of allochthonous DOM in the epilimnion and autotrophic production of DOM by bacteria in the hypolimnion cause seasonal trends in the UV absorbance of lakes.

Chemical and isotopic composition of marine organic matter as indicators of its origin

International Nuclear Information System (INIS)

Malej, A.

1989-07-01

The present study was carried out to evaluate the relative importance of marine and terrestrial sources of Particulate Organic Matter (POM) in the Northern Adriatic Sea. Samples of POM were obtained from the water column at 14 stations using Niskin bottles at 4 depths and sediment traps (placed near the sea floor). Additional samples were obtained of likely source organic matter: sewage, river POM, phytoplankton bloom material, zooplankton, jelly-fish and bethic macrophytes. All samples were analyzed for total carbon and nitrogen and the delta C-13/C-12 ratio (by mass spectrometry). Marine and terrestrial sources of POM were clearly distinguished by their isotopic ratios. A linear model was set up to evaluate the relative importance of these sources at each sampling station. Except in the immediate vicinity of river sources, the marine component appears to dominate. 7 refs, 5 figs, 1 tab

Origin and fate of organic matter in sandy soils along a primary vegetation succession

NARCIS (Netherlands)

Nierop, K.

1999-01-01

Until now little is known about the role vegetation plays in the organic matter formation, particularly at the molecular level. Most ecosystems have a long history, which is unknown or too complex to find distinct relations between vegetation and the chemical composition of soil organic

Lead sequestration and species redistribution during soil organic matter decomposition

Science.gov (United States)

Schroth, A.W.; Bostick, B.C.; Kaste, J.M.; Friedland, A.J.

2008-01-01

The turnover of soil organic matter (SOM) maintains a dynamic chemical environment in the forest floor that can impact metal speciation on relatively short timescales. Here we measure the speciation of Pb in controlled and natural organic (O) soil horizons to quantify changes in metal partitioning during SOM decomposition in different forest litters. We provide a link between the sequestration of pollutant Pb in O-horizons, estimated by forest floor Pb inventories, and speciation using synchrotron-based X-ray fluorescence and X-ray absorption spectroscopy. When Pb was introduced to fresh forest Oi samples, it adsorbed primarily to SOM surfaces, but as decomposition progressed over two years in controlled experiments, up to 60% of the Pb was redistributed to pedogenic birnessite and ferrihydrite surfaces. In addition, a significant fraction of pollutant Pb in natural soil profiles was associated with similar mineral phases (???20-35%) and SOM (???65-80%). Conifer forests have at least 2-fold higher Pb burdens in the forest floor relative to deciduous forests due to more efficient atmospheric scavenging and slower organic matter turnover. We demonstrate that pedogenic minerals play an important role in surface soil Pb sequestration, particularly in deciduous forests, and should be considered in any assessment of pollutant Pb mobility. ?? 2008 American Chemical Society.

Mapping Soil Organic Matter with Hyperspectral Imaging

Science.gov (United States)

Moni, Christophe; Burud, Ingunn; Flø, Andreas; Rasse, Daniel

2014-05-01

Soil organic matter (SOM) plays a central role for both food security and the global environment. Soil organic matter is the 'glue' that binds soil particles together, leading to positive effects on soil water and nutrient availability for plant growth and helping to counteract the effects of erosion, runoff, compaction and crusting. Hyperspectral measurements of samples of soil profiles have been conducted with the aim of mapping soil organic matter on a macroscopic scale (millimeters and centimeters). Two soil profiles have been selected from the same experimental site, one from a plot amended with biochar and another one from a control plot, with the specific objective to quantify and map the distribution of biochar in the amended profile. The soil profiles were of size (30 x 10 x 10) cm3 and were scanned with two pushbroomtype hyperspectral cameras, one which is sensitive in the visible wavelength region (400 - 1000 nm) and one in the near infrared region (1000 - 2500 nm). The images from the two detectors were merged together into one full dataset covering the whole wavelength region. Layers of 15 mm were removed from the 10 cm high sample such that a total of 7 hyperspectral images were obtained from the samples. Each layer was analyzed with multivariate statistical techniques in order to map the different components in the soil profile. Moreover, a 3-dimensional visalization of the components through the depth of the sample was also obtained by combining the hyperspectral images from all the layers. Mid-infrared spectroscopy of selected samples of the measured soil profiles was conducted in order to correlate the chemical constituents with the hyperspectral results. The results show that hyperspectral imaging is a fast, non-destructive technique, well suited to characterize soil profiles on a macroscopic scale and hence to map elements and different organic matter quality present in a complete pedon. As such, we were able to map and quantify biochar in our

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

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,...

Soil erosion and organic matter loss by using fallout 137Cs as tracer in Miyun reservoir valley

International Nuclear Information System (INIS)

Hua Luo; Zhang Zhigang; Li Junbo; Feng Yan; Zhao Hong; Yin Xunxiao; Zhu Fengyun

2005-01-01

Miyun reservoir is one of the important water sources for Beijing, the water quality of the reservoir is directly influenced by soil erosion. Based on measuring the 137 Cs concentrations, organic content in the soil of selected sampling sites, the authors investigated the relationship between the quality of soil erosion and organic matters. According to classificatory standards of soil erosion, the intensity of erosion in Miyun reservoir valley is light and moderate, but in some parts erosion is serious. The land use model has dramatic influence on distribution of organic matters in the soil. Unreasonable human activities could cause serious increase of organic matter runoff and soil erosion intensity. Distributions of organic matters were increased in the following order: bush land > forestry > orchard > farmland. Organic matters in the upper course were higher than in the circumference of reservoir. The simulated model suggests that there is a cubic relation between the contents of organic matters and 137 Cs concentrations (r 2 =0.9). The math model in the single sights can forecast soil erosion and changes of concentrations of organic matters in the soils, so that the chemical analysis and measurements are simplified. (authors)

Characterization of insoluble organic matter in primitive meteorites by microRaman spectroscopy

Science.gov (United States)

Busemann, Henner; Alexander, M. O'd.; Nittler, Larry R.

2007-08-01

We have analyzed the chemically and isotopically well-characterized insoluble organic matter (IOM) extracted from 51 unequilibrated chondrites (8 CR, 9 CM, 1 CI, 3 ungrouped C, 9 CO, 9 CV, 10 ordinary, 1 CB and 1 E chondrites) using confocal imaging Raman spectroscopy. The average Raman properties of the IOM, as parameterized by the peak characteristics of the so-called D and G bands, which originate from aromatic C rings, show systematic trends that are correlated with meteorite (sub-) classification and IOM chemical compositions. Processes that affect the Raman and chemical properties of the IOM, such as thermal metamorphism experienced on the parent bodies, terrestrial weathering and amorphization due to irradiation in space, have been identified. We established separate sequences of metamorphism for ordinary, CO, oxidized, and reduced CV chondrites. Several spectra from the most primitive chondrites reveal the presence of organic matter that has been amorphized. This amorphization, usually the result of sputtering processes or UV or particle irradiation, could have occurred during the formation of the organic material in interstellar or protoplanetary ices or, less likely, on the surface of the parent bodies or during the transport of the meteorites to Earth. D band widths and peak metamorphic temperatures are strongly correlated, allowing for a straightforward estimation of these temperatures.

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.

Assessment of soil properties by organic matter and EM-microorganism incorporation

Directory of Open Access Journals (Sweden)

Valarini P. J.

2003-01-01

Full Text Available Properties of a claim loam soil, collected in Aranjuez (Madrid and enriched with organic matter and microorganisms, were evaluated under controlled temperature and moisture conditions, over a period of three months. The following treatments were carried out: soil (control; soil + 50 t ha-1 of animal manure (E50; soil + 50 t ha-1 of animal manure + 30 L ha-1 of effective microorganisms (E50EM; soil + 30 t ha-1 of the combination of various green crop residues and weeds (RC30 and soil + 30 t ha-1 of the combination of various green crop residues and weeds + 30 L ha-1 of effective microorganisms (RC30EM. Soil samples were taken before and after incubation and their physical, chemical, and microbiological parameters analyzed. Significant increase was observed in the production of exopolysaccharides and basic phosphatase and esterase enzyme activities in the treatments E50EM and RC30EM, in correlation with the humification of organic matter, water retention at field capacity, and the cationic exchange capacity (CEC of the same treatments. The conclusion was drawn that the incorporation of a mixture of effective microorganisms (EM intensified the biological soil activity and improved physical and chemical soil properties, contributing to a quick humification of fresh organic matter. These findings were illustrated by the microbiological activities of exopolysaccharides and by alkaline phosphatase and esterase enzymes, which can be used as early and integrated soil health indicators.

Non disturbing characterization and quantification of natural organic matter (NOM) contained in clay rock pore water by mass spectrometry using electro-spray and atmospheric pressure chemical ionization modes

International Nuclear Information System (INIS)

Huclier-Markai, S.; Landesman, C.; Grambow, B.; Rogniaux, H.; Monteau, F.; Vinsot, A.

2010-01-01

Document available in extended abstract form only. The Callovo-Oxfordian formation (COx) rock may contain up to 1% w/w of organic Carbon. Most of the Organic Matter (OM) is attached to the mineral particles whereas a small portion is present as Dissolved Organic Matter (DOM) in the pore water. In environmental studies, Natural Organic Matter (NOM) plays a key role on the bioavailability and the toxicity of metallic compounds. It is necessary to know the structure of any organic substance in order to assess which chemical and biological reactions occur under environmentally relevant conditions. The 150 Myears solid-bound organic matter of the COx (kerogen) has been already investigated in several studies and originates from a mixture of marine and terrestrial sources. In addition to this, the CCl 4 soluble organic fraction (bitumen) has been already characterized by liquid and gas chromatography coupled to mass spectrometry. It allows proportion and distribution of biological markers to be determined as polar compounds with aromatic and saturated hydrocarbons. DOM was extracted from a crushed clay rock of the COx formation with a high rock/water ratio of about 1500 g/L. Part of the OM from the COx is known to be sensitive to air oxidation which can significantly modify the nature of the bitumen by an overall shift towards lower molecular weight compounds. Therefore, the characteristics of the DOM must be determined in in-situ like conditions if one wants to assess the mobility of DOM in the clay pore space and to evaluate the mobility of heavy metals/ radionuclides. Due to their high binding capacity with metal ions and their colloidal sizes in natural waters, these macromolecules, through complexation reactions, might either enhance the mobility of trace elements, or reduce their migration rates by sorption processes in relation with their size and that of the porous medium. Consequently, the characterization of DOM in anoxic pore water samples from the COx

Organic matter in central California radiation fogs.

Science.gov (United States)

Herckes, Pierre; Lee, Taehyoung; Trenary, Laurie; Kang, Gongunn; Chang, Hui; Collett, Jeffrey L

2002-11-15

Organic matter was studied in radiation fogs in the San Joaquin Valley of California during the California Regional Particulate Air Quality Study (CRPAQS). Total organic carbon (TOC) concentrations ranged from 2 to 40 ppm of C. While most organic carbon was found in solution as dissolved organic carbon (DOC), 23% on average was not dissolved inside the fog drops. We observe a clear variation of organic matter concentration with droplet size. TOC concentrations in small fog drops (fogwater, consistent with the enrichment of the organic matter in smaller fog drops with lower terminal settling velocities.

Combined organic matter and nitrogen removal from a chemical industry wastewater in a two-stage MBBR system.

Science.gov (United States)

Cao, S M S; Fontoura, G A T; Dezotti, M; Bassin, J P

2016-01-01

Pesticide-producing factories generate highly polluting wastewaters containing toxic and hazardous compounds which should be reduced to acceptable levels before discharge. In this study, a chemical industry wastewater was treated in a pre-denitrification moving-bed biofilm reactor system subjected to an increasing internal mixed liquor recycle ratio from 2 to 4. Although the influent wastewater characteristics substantially varied over time, the removal of chemical oxygen demand (COD) and dissolved organic carbon was quite stable and mostly higher than 90%. The highest fraction of the incoming organic matter was removed anoxically, favouring a low COD/N environment in the subsequent aerobic nitrifying tank and thus ensuring stable ammonium removal (90-95%). However, during pH and salt shock periods, nitrifiers were severely inhibited but gradually restored their full nitrifying capability as non-stressing conditions were reestablished. Besides promoting an increase in the maximum nitrification potential of the aerobic attached biomass from 0.34 to 0.63 mg [Formula: see text], the increase in the internal recycle ratio was accompanied by an increase in nitrogen removal (60-78%) and maximum specific denitrification rate (2.7-3.3 mg NOx(-)--N). Total polysaccharides (PS) and protein (PT) concentrations of attached biomass were observed to be directly influenced by the influent organic loading rate, while the PS/PT ratio mainly ranged from 0.3 to 0.5. Results of Microtox tests showed that no toxicity was found in the effluent of both the anoxic and aerobic reactors, indicating that the biological process was effective in removing residual substances which might adversely affect the receiving waters' ecosystem.

Micro-Scale Characteristics of Insoluble Organic Matter in Chondrites: A Coordinated TEM, STXM and SIMS Study

Science.gov (United States)

Nittler, L. R.; Alexander, C. M. O'd.; Cody, G. D.; de Gregorio, B. T.; Kilcoyne, A. L. D.; Stroud, R. M.; Tiwari, A.

2009-03-01

A coordinated study of meteoritic insoluble organic matter reveals that hollow organic globules are chemically similar to other IOM, but abundances and sizes of globules vary between meteorites. IOM is sensitive to electron and X-ray induced beam damage.

Chemical compositions and sources of organic matter in fine particles of soils and sands from the vicinity of Kuwait city.

Science.gov (United States)

Rushdi, Ahmed I; Al-Zarban, Sheikha; Simoneit, Bernd R T

2006-09-01

Fine particles in the atmosphere from soil and sand resuspension contain a variety of organic compounds from natural biogenic and anthropogenic matter. Soil and sand samples from various sites near Kuwait city were collected, sieved to retain the fine particles, and extracted with a mixture of dichloromethane and methanol. The extracts were derivatized and analyzed by gas chromatography-mass spectrometry in order to characterize the chemical compositions and sources of the organic components. The major inputs of organic compounds were from both natural biogenic and anthropogenic sources in these samples. Vegetation was the major natural source of organic compounds and included n-alkanols, n-alkanoic acids, n-alkanes, sterols and triterpenoids. Saccharides had high concentrations (31-43%) in the sand dune and seafront samples, indicating sources from decomposed vegation materials and/or the presence of viable microbiota such as bacteria and fungi. Vehicular emission products, leakage of lubricating oils, discarded plastics and emissions from cooking operations were the major anthropogenic inputs in the samples from the urban areas. This input was mainly UCM, n-alkanes, hopanes, plasticizers and cholesterol, respectively.

Podzolisation and soil organic matter dynamics

NARCIS (Netherlands)

Buurman, P.; Jongmans, A.G.

2005-01-01

Present models of podzolisation emphasize the mobilization and precipitation of dissolved organic matter. together with Al(-silicates) and Fe. Such models cannot explain the dominance of pellet-like organic matter in most boreal podzols and in well-drained podzols outside the boreal zone, and the

Influence of organic matter on the solubility of ThO2 and geochemical modeling

International Nuclear Information System (INIS)

Liu Dejun; Luo Tian; Maes, N.; Bruggeman, C.

2014-01-01

Thorium (IV) is widely considered in laboratory experiments as a suitable chemical analogue for long-lived tetravalent actinides. Th (IV) is redox-insensitive, as an analogue for U (IV) to study the influence of natural organic matter on the solubility. The solubility of crystalline ThO 2 (cr) has been measured under geochemical conditions representative for the Boom Clay using Real Boom Clay Water containing organic matter to assess its influence on the ThO 2 (cr) solubility. For the purpose of comparison, Aldrich Humic Acid was also investigated. Solubility measurements of ThO 2 (cr) were approached from under-saturation in an anaerobic glove box with a controlled Ar0.4%CO 2 atmosphere. Th concentration is determined after 30000 MWCO, 300000 MWCO, and 0.45 μm filtration to distinguish solid (0.45 μm), larger colloids (300000 MWCO), and small dissolved species(30000 MWCO). X-ray diffraction was carried out to investigate the transformation of ThO 2 (cr) phase during the contact with Boom Clay Water. In Synthetic Boom Clay Water (without organic matter) the concentrations of Th (IV) are 5 × l0 -ll mol/L, 4 × lO -10 mol/L, and 8 × lO -8 mol/L after 30000 MWCO, 300000 MWCO, and 0. 45 μm filtration, respectively. It indicated the existence of inorganic colloids in solution. The increase of the total Th solution concentration with increasing organic matter concentration revealed a complexation-like interaction between Th and organic matter. All the experimental data could be modeled by Tipping humic ion-binding model VI using a combination of solubility calculations and complexation reactions between Th (IV) and organic matter functional groups. Similar to the investigation of Eu 3+ solubility, the affinity of organic matter for Th was higher for Aldrich humic acid compared to Boom Clay organic matter. However, Boom Clay organic matter with different size had the similar complexation affinity with Th (IV). (authors)

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.

Estimating pesticide sampling rates by the polar organic chemical integrative sampler (POCIS) in the presence of natural organic matter and varying hydrodynamic conditions

International Nuclear Information System (INIS)

Charlestra, Lucner; Amirbahman, Aria; Courtemanch, David L.; Alvarez, David A.; Patterson, Howard

2012-01-01

The polar organic chemical integrative sampler (POCIS) was calibrated to monitor pesticides in water under controlled laboratory conditions. The effect of natural organic matter (NOM) on the sampling rates (R s ) was evaluated in microcosms containing −1 of total organic carbon (TOC). The effect of hydrodynamics was studied by comparing R s values measured in stirred (SBE) and quiescent (QBE) batch experiments and a flow-through system (FTS). The level of NOM in the water used in these experiments had no effect on the magnitude of the pesticide sampling rates (p > 0.05). However, flow velocity and turbulence significantly increased the sampling rates of the pesticides in the FTS and SBE compared to the QBE (p < 0.001). The calibration data generated can be used to derive pesticide concentrations in water from POCIS deployed in stagnant and turbulent environmental systems without correction for NOM. - Highlights: ► We assessed the effect of TOC and stirring on pesticide sampling rates by POCIS. ► Total organic carbon (TOC) had no effect on the sampling rates. ► Water flow and stirring significantly increased the magnitude of the sampling rates. ► The sampling rates generated are directly applicable to field conditions. - This study provides POCIS sampling rates data that can be used to estimate freely dissolved concentrations of toxic pesticides in natural waters.

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

Science.gov (United States)

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

Unraveling the size-dependent optical properties of dissolved organic matter

DEFF Research Database (Denmark)

Wünsch, Urban; Stedmon, Colin; Tranvik, Lars

2018-01-01

The size-dependent optical properties of dissolved organic matter (DOM) from four Swedish lakes were investigated using High Performance Size Exclusion Chromatography (HPSEC) in conjunction with online characterization of absorbance (240–600 nm) and fluorescence (excitation: 275 nm, emission: 300....... This study demonstrates the potential for HPSEC and novel mathematical approaches to provide unprecedented insights into the relationship between optical and chemical properties of DOM in aquatic systems...

When Organization Fails: Why Authority Matters

DEFF Research Database (Denmark)

Blaschke, Steffen

2015-01-01

Review of: James R. Taylor and Elizabeth J. Van Every / When Organization Fails: Why Authority Matters. (New York: Routledge, 2014. 220 pp. ISBN: 978 0415741668)......Review of: James R. Taylor and Elizabeth J. Van Every / When Organization Fails: Why Authority Matters. (New York: Routledge, 2014. 220 pp. ISBN: 978 0415741668)...

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)

Interaction of extrinsic chemical factors affecting photodegradation of dissolved organic matter in aquatic ecosystems

Czech Academy of Sciences Publication Activity Database

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

2014-01-01

Roč. 13, č. 5 (2014), s. 799-812 ISSN 1474-905X R&D Projects: GA ČR(CZ) GAP503/12/0781 Institutional support: RVO:60077344 Keywords : photodegradation * dissolved organic matter * calcium * nitrate * iron * pH Subject RIV: DA - Hydrology ; Limnology Impact factor: 2.267, year: 2014

Chemical characterization of organic particulate matter from on-road traffic in Sao Paulo, Brazil

NARCIS (Netherlands)

Oyama, Beatriz Sayuri; Andrade, Maria de Fatima; Herckes, Pierre; Dusek, Ulrike; Rockmann, Thomas; Holzinger, Rupert

2016-01-01

This study reports emission of organic particulate matter by light-duty vehicles (LDVs) and heavy-duty vehicles (HDVs) in the city of Sao Paulo, Brazil, where vehicles run on three different fuel types: gasoline with 25% ethanol (called gasohol, E25), hydrated ethanol (E100), and diesel (with 5%

Using soil organic matter fractions as indicators of soil physical quality

DEFF Research Database (Denmark)

Pulido Moncada, Mansonia A.; Lozano, Z; Delgado, M

2018-01-01

The objective of this study was to evaluate the use of chemical and physical fractions of soil organic matter (SOM), rather than SOM per se, as indicators of soil physical quality (SPQ) based on their effect on aggregate stability (AS). Chemically extracted humic and fulvic acids (HA and FA) were...... used as chemical fractions, and heavy and light fractions (HF and LF) obtained by density separation as physical fractions. The analyses were conducted on medium-textured soils from tropical and temperate regions under cropland and pasture. Results show that soil organic carbon (SOC), SOM fractions...... and AS appear to be affected by land use regardless of the origin of the soils. A general separation of structurally stable and unstable soils between samples of large and small SOC content, respectively, was observed. SOM fractions did not show a better relationship with AS than SOC per se. In both...

Photobiogeochemistry of organic matter. Principles and practices in water environments

Energy Technology Data Exchange (ETDEWEB)

Mostofa, Khan M.G. [Chinese Academy of Sciences, Guiyang, Guizhou (China). Inst. of Geochemistry; Yoshioka, Takahito [Kyoto Univ. (Japan). Field Science Education; Mottaleb, M. Abdul [Northwest Missouri State Univ., MO (United States). Dept. of Chemistry and Physics; Vione, Davide (eds.) [Turin Univ. (Italy). Dipt. di Chimica Analitica

2013-03-01

Gives a comprehensive account of photo and biological processes of key biogeochemical functions and their interrelations in the aquatic environment. Discusses essential issues refering to the aquatic environment. Designed as a study text for students. Photoinduced processes, caused by natural sunlight, are key functions for sustaining all living organisms through production and transformation of organic matter (OM) in the biosphere. Production of hydrogen peroxide (H2O2) from OM is a primary step of photoinduced processes, because H2O2 acts as strong reductant and oxidant. It is potentially important in many aquatic reactions, also in association with photosynthesis. Allochthonous and autochthonous dissolved organic matter (DOM) can be involved into several photoinduced or biological processes. DOM subsequently undergoes several physical, chemical, photoinduced and biological processes, which can be affected by global warming. This book is uniquely structured to overview some vital issues, such as: DOM; H2O2 and ROOH; HO x; Degradation of DOM; CDOM, FDOM; Photosynthesis; Chlorophyll; Metal complexation, and Global warming, as well as their mutual interrelationships, based on updated scientific results''.

Natural organic matter to enhance electrokinetic transport of PAH

Energy Technology Data Exchange (ETDEWEB)

Suer, P.; Joensson, S.; Allard, B. [Man-Technology-Environment Research Centre, Oerebro Univ. (Sweden)

2001-07-01

The remediation of contaminated soil can be enhanced with natural organic matter (NOM) as a complexing agent for pollutants. NOM has both hydrophobic and acidic properties, so that it is charged and thus subject to electroremediation. At the same time many contaminants have a high affinity for organic matter. Organic matter was produced in situ in an electric field or added in solute form. The resulting dissolved organic matter was transported towards the cathode, probably by cationic colloids. Produced dissolved organic matter included high molecular weight molecules near the cathode, at the site of pH buffering. Pyrene and phenanthrene were likewise transported towards the cathode. Movement was small but distinctive in 2-day experiments. Clay influence the soil/water distribution of the PAH but no effect on the total transport could be discerned. The presence of solid organic matter in the soil removed all PAH from the water phase, even though the concentration of organic matter in the water phase was high as well. (orig.)

Stabilization of organic matter in the raised-bed soils of tidal swamplands is influenced by the types and the amounts of organic matter application

Directory of Open Access Journals (Sweden)

A R Saidy

2015-05-01

Full Text Available Farmers in tidal swamplands annually added organic matter (OM onto the raised beds to maintain organic matter contents and thereby maintain soil productivity of the raised beds. This experiment aimed to study the influence of the types and the amounts of OM on the stabilization of organic matter in the raised-bed soils. Four types of OM: rice straw, eceng gondok (Eichornia crassipes, purun tikus  (Eleocharis dulcis and mixed  rice straw-eceng gondok were added to a 27-year raised bed soil with 4 different rates: 0, 0.5, 1.0 and 2.0  of maximum sorption capacity (Qmax, and the OM stabilization was quantified after 10 weeks of OM addition.  Results of this study showed with the exception of rice straw, OM addition to soil resulted in increases in the mineralization of soil OM thereby inducing priming effect. Addition of rice straw at rate of 0.5 of Qmax resulted in stabilization of 46% added OM, while only 30% and 37% of added OM was stabilized when OM was added to soils at rates of 1.0 and 2.0 Qmax, respectively.  This study showed that the stabilization of OM in raised bed soils were influenced by the chemical composition of OM and the amount of added OM.

Stabilization of organic matter in the raised-bed soils of tidal swamplands is influenced by the types and the amounts of organic matter application

Directory of Open Access Journals (Sweden)

A R Saidy

2015-03-01

Full Text Available Farmers in tidal swamplands annually added organic matter (OM onto the raised beds to maintain organic matter contents and thereby maintain soil productivity of the raised beds. This experiment aimed to study the influence of the types and the amounts of OM on the stabilization of organic matter in the raised-bed soils. Four types of OM: rice straw, eceng gondok (Eichornia crassipes, purun tikus  (Eleocharis dulcis and mixed  rice straw-eceng gondok were added to a 27-year raised bed soil with 4 different rates: 0, 0.5, 1.0 and 2.0  of maximum sorption capacity (Qmax, and the OM stabilization was quantified after 10 weeks of OM addition.  Results of this study showed with the exception of rice straw, OM addition to soil resulted in increases in the mineralization of soil OM thereby inducing priming effect. Addition of rice straw at rate of 0.5 of Qmax resulted in stabilization of 46% added OM, while only 30% and 37% of added OM was stabilized when OM was added to soils at rates of 1.0 and 2.0 Qmax, respectively.  This study showed that the stabilization of OM in raised bed soils were influenced by the chemical composition of OM and the amount of added OM.

Mineral surface–organic matter interactions: basics and applications

International Nuclear Information System (INIS)

Valdrè, G; Moro, D; Ulian, G

2012-01-01

The ability to control the binding of biological and organic molecules to a crystal surface is central in several fields; for example, in biotechnology, catalysis, molecular microarrays, biosensors preparation and environmental sciences. The nano-morphology and nanostructure at the surface may have physico-chemical properties that are very different from those of the underlying mineral substrate. Recent developments in scanning probe microscopy (SPM) have widened the spectrum of possible investigations that can be performed at the nanometric level on the surface of minerals. They range from the study of physical properties such as surface potential, electric field topological determination, Brønsted–Lowry site distributions, to chemical and spectroscopic analysis in air, in liquid or in gaseous environments. After an introduction to SPM modes of operation and new SPM-based technological developments, we will present recent examples of applications in the study of interactions between organic matter and mineral surface and report on the advances in knowledge that have been made by the use of scanning probe microscopy.

Old and stable soil organic matter is not necessarily chemically recalcitrant: Implications for modeling concepts and temperature sensitivity

Energy Technology Data Exchange (ETDEWEB)

Kleber, M.; Nico, P.S.; Plante, A.; Filley, T.; Kramer, M.; Swanston, C.; Sollins, P.

2010-03-01

Soil carbon turnover models generally divide soil carbon into pools with varying intrinsic decomposition rates. Although these decomposition rates are modified by factors such as temperature, texture, and moisture, they are rationalized by assuming chemical structure is a primary controller of decomposition. In the current work, we use near edge X-ray absorption fine structure (NEXAFS) spectroscopy in combination with differential scanning calorimetry (DSC) and alkaline cupric oxide (CuO) oxidation to explore this assumption. Specifically, we examined material from the 2.3-2.6 kg L{sup -1} density fraction of three soils of different type (Oxisol, Alfisol, Inceptisol). The density fraction with the youngest {sup 14}C age (Oxisol, 107 years) showed the highest relative abundance of aromatic groups and the lowest O-alkyl C/aromatic C ratio as determined by NEXAFS. Conversely, the fraction with the oldest C (Inceptisol, 680 years) had the lowest relative abundance of aromatic groups and highest O-alkyl C/aromatic C ratio. This sample also had the highest proportion of thermally labile materials as measured by DSC, and the highest ratio of substituted fatty acids to lignin phenols as indicated by CuO oxidation. Therefore, the organic matter of the Inceptisol sample, with a {sup 14}C age associated with 'passive' pools of carbon (680 years), had the largest proportion of easily metabolizable organic molecules with low thermodynamic stability, whereas the organic matter of the much younger Oxisol sample (107 years) had the highest proportion of supposedly stable organic structures considered more difficult to metabolize. Our results demonstrate that C age is not necessarily related to molecular structure or thermodynamic stability, and we suggest that soil carbon models would benefit from viewing turnover rate as codetermined by the interaction between substrates, microbial actors, and abiotic driving variables. Furthermore, assuming that old carbon is composed

Visualising the equilibrium distribution and mobility of organic contaminants in soil using the chemical partitioning space.

Science.gov (United States)

Wong, Fiona; Wania, Frank

2011-06-01

Assessing the behaviour of organic chemicals in soil is a complex task as it is governed by the physical chemical properties of the chemicals, the characteristics of the soil as well as the ambient conditions of the environment. The chemical partitioning space, defined by the air-water partition coefficient (K(AW)) and the soil organic carbon-water partition coefficient (K(OC)), was employed to visualize the equilibrium distribution of organic contaminants between the air-filled pores, the pore water and the solid phases of the bulk soil and the relative importance of the three transport processes removing contaminants from soil (evaporation, leaching and particle erosion). The partitioning properties of twenty neutral organic chemicals (i.e. herbicides, pharmaceuticals, polychlorinated biphenyls and volatile chemicals) were estimated using poly-parameter linear free energy relationships and superimposed onto these maps. This allows instantaneous estimation of the equilibrium phase distribution and mobility of neutral organic chemicals in soil. Although there is a link between the major phase and the dominant transport process, such that chemicals found in air-filled pore space are subject to evaporation, those in water-filled pore space undergo leaching and those in the sorbed phase are associated with particle erosion, the partitioning coefficient thresholds for distribution and mobility can often deviate by many orders of magnitude. In particular, even a small fraction of chemical in pore water or pore air allows for evaporation and leaching to dominate over solid phase transport. Multiple maps that represent soils that differ in the amount and type of soil organic matter, water saturation, temperature, depth of surface soil horizon, and mineral matters were evaluated.

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.

Chemical characterization of organic particulate matter from on-road traffic in Sao Paulo, Brazil

NARCIS (Netherlands)

Oyama, Beatriz Sayuri; Andrade, Maria de Fatima; Herckes, Pierre; Dusek, Ulrike; Rockmann, Thomas; Holzinger, Rupert

2016-01-01

This study reports emission of organic particulate matter by light-duty vehicles (LDVs) and heavy-duty vehicles (HDVs) in the city of São Paulo, Brazil, where vehicles run on three different fuel types: gasoline with 25 % ethanol (called gasohol, E25), hydrated ethanol (E100), and diesel (with 5 %

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)

Molybdenum isotope fractionation during adsorption to organic matter

Science.gov (United States)

King, Elizabeth K.; Perakis, Steven; Pett-Ridge, Julie C.

2018-01-01

Organic matter is of emerging interest as a control on molybdenum (Mo) biogeochemistry, and information on isotope fractionation during adsorption to organic matter can improve interpretations of Mo isotope variations in natural settings. Molybdenum isotope fractionation was investigated during adsorption onto insolubilized humic acid (IHA), a surrogate for organic matter, as a function of time (2–170 h) and pH (2–7). For the time series experiment performed at pH 4.2, the average Mo isotope fractionation between the solution and the IHA (Δ98Mosolution-IHA) was 1.39‰ (± 0.16‰, 2σ, based on 98Mo/95Mo relative to the NIST 3134 standard) at steady state. For the pH series experiment, Mo adsorption decreased as pH increased from 2.0 to 6.9, and the Δ98Mosolution-IHA increased from 0.82‰ to 1.79‰. We also evaluated natural Mo isotope patterns in precipitation, foliage, organic horizon, surface mineral soil, and bedrock from 12 forested sites in the Oregon Coast Range. The average Mo isotope offset observed between precipitation and organic (O) horizon soil was 2.1‰, with light Mo isotopes adsorbing preferentially to organic matter. Fractionation during adsorption to organic matter is similar in magnitude and direction to prior observations of Mo fractionation during adsorption to Fe- and Mn- (oxyhydr)oxides. Our finding that organic matter influences Mo isotope composition has important implications for the role of organic matter as a driver of trace metal retention and isotopic fractionation.

Organic and chemical manure of the bean (Phaseolus vulgaris) in alluvial soils of intermediate climate

International Nuclear Information System (INIS)

Tamayo V, Alvaro; Munoz A, Rodrigo

1997-01-01

With the purpose to evaluate the effect on bean production ICA CITARA variety, four sources of organic matter (hen manure, pig manure, cow manure, and earthworm manure) in four doses 280,500 y 1.000 kg/ha with the same doses of chemical fertilization, were evaluated the experiment was carried out at Tulio Ospina Research Center, located at Bello (Antioquia) of medium climate with 1.320 m.s.n.m. This was established using an alluvial soil (Tropofluvent), frenk, with low contents of organic, matter (2,2%), phosphorus (10 ppm), and potassium (0,10 meq/l00 g). the results, after six consecutive harvests on the same plots, showed highly significative differences among treatments. The highest yield (1.836 kg/ha) was obtained when to the chemical fertilization (300 kg of 10-30-10) was added with 250 kg/ha of hen manure, followed by the application of 100 kg/ha, of cow manure (1.812 kg/ha). Chemical fertilization without organic matter produced 1.640 kg/ha of bean, which was very similar to the addition of 1.000 kg/ha of cow manure and earthworm manure with yields of 1.688 kg/ha and 1.635 kg/ha respectively

Changes in the chemical characteristics of water-extracted organic matter from vermicomposting of sewage sludge and cow dung

Energy Technology Data Exchange (ETDEWEB)

Xing, Meiyan, E-mail: xingmeiyan@tongji.edu.cn [State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China); Li, Xiaowei; Yang, Jian; Huang, Zhidong; Lu, Yongsen [State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China)

2012-02-29

Highlights: Black-Right-Pointing-Pointer Vermicomposting causes an increase in the aromaticity of WEOM from the substrates. Black-Right-Pointing-Pointer Vermicomposting homogenizes the molecular weight of WEOM from the substrates. Black-Right-Pointing-Pointer The WEOM from the vermicompost is characterized by high O-containing groups. Black-Right-Pointing-Pointer The WEOM from the vermicompost includes small aliphatic and protein-like groups. Black-Right-Pointing-Pointer The WEOM test is a good way to evaluate the biological maturity of vermicompost. - Abstract: The chemical changes of water-extractable organic matter (WEOM) from five different substrates of sewage sludge enriched with different proportions of cow dung after vermicomposting with Eisenia fetida were investigated using various analytical approaches. Results showed that dissolved organic carbon, chemical oxygen demand, and C/N ratio of the substrates decreased significantly after vermicomposting process. The aromaticity of WEOM from the substrates enhanced considerably, and the amount of volatile fatty acids declined markedly, especially for the cow dung substrate. Gel filtration chromatography analysis showed that the molecular weight fraction between 10{sup 3} and 10{sup 6} Da became the main part of WEOM in the final product. {sup 1}H nuclear magnetic resonance spectra revealed that the proportion of H moieties in the area of 0.00-3.00 ppm decreased, while increasing at 3.00-4.25 ppm after vermicomposting. Fluorescence spectra indicated that vermicomposting caused the degradation of protein-like groups, and the formation of fulvic and humic acid-like compounds in the WEOM of the substrates. Overall results indicate clearly that vermicomposting promoted the degradation and transformation of liable WEOM into biological stable substances in sewage sludge and cow dung alone, as well as in mixtures of both materials, and testing the WEOM might be an effective way to evaluate the biological maturity and

Changes in the chemical characteristics of water-extracted organic matter from vermicomposting of sewage sludge and cow dung

International Nuclear Information System (INIS)

Xing, Meiyan; Li, Xiaowei; Yang, Jian; Huang, Zhidong; Lu, Yongsen

2012-01-01

Highlights: ► Vermicomposting causes an increase in the aromaticity of WEOM from the substrates. ► Vermicomposting homogenizes the molecular weight of WEOM from the substrates. ► The WEOM from the vermicompost is characterized by high O-containing groups. ► The WEOM from the vermicompost includes small aliphatic and protein-like groups. ► The WEOM test is a good way to evaluate the biological maturity of vermicompost. - Abstract: The chemical changes of water-extractable organic matter (WEOM) from five different substrates of sewage sludge enriched with different proportions of cow dung after vermicomposting with Eisenia fetida were investigated using various analytical approaches. Results showed that dissolved organic carbon, chemical oxygen demand, and C/N ratio of the substrates decreased significantly after vermicomposting process. The aromaticity of WEOM from the substrates enhanced considerably, and the amount of volatile fatty acids declined markedly, especially for the cow dung substrate. Gel filtration chromatography analysis showed that the molecular weight fraction between 10 3 and 10 6 Da became the main part of WEOM in the final product. 1 H nuclear magnetic resonance spectra revealed that the proportion of H moieties in the area of 0.00–3.00 ppm decreased, while increasing at 3.00–4.25 ppm after vermicomposting. Fluorescence spectra indicated that vermicomposting caused the degradation of protein-like groups, and the formation of fulvic and humic acid-like compounds in the WEOM of the substrates. Overall results indicate clearly that vermicomposting promoted the degradation and transformation of liable WEOM into biological stable substances in sewage sludge and cow dung alone, as well as in mixtures of both materials, and testing the WEOM might be an effective way to evaluate the biological maturity and chemical stability of vermicompost.

Highly Viscous States Affect the Browning of Atmospheric Organic Particulate Matter.

Science.gov (United States)

Liu, Pengfei; Li, Yong Jie; Wang, Yan; Bateman, Adam P; Zhang, Yue; Gong, Zhaoheng; Bertram, Allan K; Martin, Scot T

2018-02-28

Initially transparent organic particulate matter (PM) can become shades of light-absorbing brown via atmospheric particle-phase chemical reactions. The production of nitrogen-containing compounds is one important pathway for browning. Semisolid or solid physical states of organic PM might, however, have sufficiently slow diffusion of reactant molecules to inhibit browning reactions. Herein, organic PM of secondary organic material (SOM) derived from toluene, a common SOM precursor in anthropogenically affected environments, was exposed to ammonia at different values of relative humidity (RH). The production of light-absorbing organonitrogen imines from ammonia exposure, detected by mass spectrometry and ultraviolet-visible spectrophotometry, was kinetically inhibited for RH atmospheric brown carbon production and associated influences on energy balance.

Nitrogen isotopic composition of macromolecular organic matter in interplanetary dust particles

Science.gov (United States)

Aléon, Jérôme; Robert, François; Chaussidon, Marc; Marty, Bernard

2003-10-01

Nitrogen concentrations and isotopic compositions were measured by ion microprobe scanning imaging in two interplanetary dust particles L2021 K1 and L2036 E22, in which imaging of D/H and C/H ratios has previously evidenced the presence of D-rich macromolecular organic components. High nitrogen concentrations of 10-20 wt% and δ 15N values up to +400‰ are observed in these D-rich macromolecular components. The previous study of D/H and C/H ratios has revealed three different D-rich macromolecular phases. The one previously ascribed to macromolecular organic matter akin the insoluble organic matter (IOM) from carbonaceous chondrites is enriched in nitrogen by one order of magnitude compared to the carbonaceous chondrite IOM, although its isotopic composition is still similar to what is known from Renazzo (δ 15N = +208‰). The correlation observed in macromolecular organic material between the D- and 15N-excesses suggests that the latter originate probably from chemical reactions typical of the cold interstellar medium. These interstellar materials preserved to some extent in IDPs are therefore macromolecular organic components with various aliphaticity and aromaticity. They are heavily N-heterosubstituted as shown by their high nitrogen concentrations >10 wt%. They have high D/H ratios >10 -3 and δ 15N values ≥ +400‰. In L2021 K1 a mixture is observed at the micron scale between interstellar and chondritic-like organic phases. This indicates that some IDPs contain organic materials processed at various heliocentric distances in a turbulent nebula. Comparison with observation in comets suggests that these molecules may be cometary macromolecules. A correlation is observed between the D/H ratios and δ 15N values of macromolecular organic matter from IDPs, meteorites, the Earth and of major nebular reservoirs. This suggests that most macromolecular organic matter in the inner solar system was probably issued from interstellar precursors and further processed

Thallium and Silver binding to dissolved organic matter

Science.gov (United States)

Benedetti, M. F.; Martin, L.; Simonucci, C.; Viollier, E.

2017-12-01

Silver (Ag) and thallium (Tl) are potential contaminants at the vicinity of mining sites and are harmful pollutants. Silver can be found in mine but also as released by the dissolution of Silver nanoparticles, a major new emerging contaminant. Tl is both lithophilic and calcophilic elements and found in sulphur ores (associated with lead, zinc, antimony…) or in rocks containing K-feldspar. Speciation of Ag and Tl is poorly known mainly due to their low concentrations in aquatic environments. Review of Ag and Tl geochemistry clearly shows a lack of quantitative information about interactions with natural organic matter. Organic ligands could play an important role in Ag or Tl bioavailability, chemical reactivity (adsorption or photo oxidation inhibition or catalysis) and hence geochemical transfers. Based on equilibrium between two solutions that are separated by a selectively permeable membrane, the so-called "Donnan membrane technique" (DMT) provides a measure of free ion concentrations. Analytes measurements are performed by HR-ICP-MS Element 2 (Thermo Scientific). Experimental setup allows the Donnan equilibrium to be reached after 100 and 120 hours for Tl. Experiments performed with purified natural organic matter allow calculating complexation constants in multiple pH conditions. With this work, we contribute new data and interpretations to an active debate on Ag and Tl geochemical modeling. In conclusion, this work brings a new view on risk assessment for mining activities.

Calculation of baryon chemical potential and strangeness chemical potential in resonance matter

International Nuclear Information System (INIS)

Fu Yuanyong; Hu Shouyang; Lu Zhongdao

2006-01-01

Based on the high energy heavy-ion collisions statistical model, the baryon chemical potential and strangeness chemical potential are calculated for resonance matter with net baryon density and net strangeness density under given temperature. Furthermore, the relationship between net baryon density, net strangeness density and baryon chemical potential, strangeness chemical potential are analyzed. The results show that baryon chemical potential and strangeness chemical potential increase with net baryon density and net strangeness density increasing, the change of net baryon density affects baryon chemical potential and strangeness chemical potential more strongly than the change of net strangeness density. (authors)

Integrated evaluation of soil quality after the incorporation of organic matter and microorganisms

Directory of Open Access Journals (Sweden)

Valarini Pedro J.

2002-01-01

Full Text Available The soil quality was evaluated following the addition of organic matter and microorganisms to a clay loam soil collected in Aranjuez (Madrid under controlled conditions of temperature and moisture, and over a period of three months. The following treatments were carried out: soil (control; soil + 50 t/ha of animal manure (E50; soil + 50 t/ha of animal manure + 30l/ha of effective microorganisms (E50EM; soil + 30 t/ha of combination of various green crop residues and weeds (RC30 and soil + 30 t/ha of combination of various green crop residues and weeds + 30l/ha of effective microorganisms (RC30EM. The soil samples were taken before and after the incubation and analysed using physical, chemical and microbiological parameters. A significant increase in the production of polysaccharides and alkaline phosphatase and esterase enzymes in the treatments E50EM and RC30EM was observed, being in direct correlation with the humification of the organic matter, with the water retention at field capacity, and with the cationic exchange capacity (CEC. It can be concluded that the incorporation of microorganisms EM potentialized the soil biological activity and improved physico-chemical soil properties, contributing to a quick humification of fresh organic matter. Those findings were proved by microbiological activities of exopolysaccharides by alcaline phosphatase and esterase enzymes, which can be used as earlier and integral soil health indicators.

Roles of epi-anecic taxa of earthworms in the organic matter recycling

Science.gov (United States)

Hoeffner, Kevin; Monard, Cécile; Santonja, Mathieu; Pérès, Guénola; Cluzeau, Daniel

2017-04-01

Given their impact on soil functioning and their interactions with soil organisms, earthworms contribute to the recycling of organic matter and participate significantly in the numerous ecosystem services provided by soils. Most studies on the role of earthworms in organic matter recycling were conducted at the level of the four functional groups (epigeic, epi-anecic, anecic strict and endogeic), but their effects at taxa level remain largely unknown. Still, within a functional group, anatomic and physiologic earthworm taxa traits are different, which should impact organic matter recycling. This study aims at determining, under controlled conditions, epi-anecic taxa differences in (i) leaf litter mass loss, (ii) assimilation and (iii) impact on microorganisms communities implied in organic matter degradation. In seperate microcosms, we chose 4 epi anecic taxa (Lumbricus rubellus, Lumbricus festivus, Lumbricus centralis and Lumbricus terrestris). Each taxon was exposed separately to leaves of three different plants (Holcus lanatus, Lolium perenne and Corylus avellana). In the same microcosm, leaves of each plant was both placed on the surface and buried 10cm deep. The experiment lasted 10 days for half of the samples and 20 days for the second half. Microorganisms communities were analysed using TRFLP in each earthworm taxon burrow walls at 20 days. We observed differences between epi-anecic taxa depending on species of plant and the duration of the experiment. Results are discussed taking into account physical and chemical properties of these 3 trophic resources (e.g. C/N ratio, phenolic compounds, percentage of lignin and cellulose...).

Influence of humified organic matter on copper behavior in acid polluted soils

International Nuclear Information System (INIS)

Fernandez-Calvino, D.; Soler-Rovira, P.; Polo, A.; Arias-Estevez, M.; Plaza, C.

2010-01-01

The main purpose of this work was to identify the role of soil humic acids (HAs) in controlling the behavior of Cu(II) in vineyard soils by exploring the relationship between the chemical and binding properties of HA fractions and those of soil as a whole. The study was conducted on soils with a sandy loam texture, pH 4.3-5.0, a carbon content of 12.4-41.0 g kg -1 and Cu concentrations from 11 to 666 mg kg -1 . The metal complexing capacity of HA extracts obtained from the soils ranged from 0.69 to 1.02 mol kg -1 , and the stability constants for the metal ion-HA complexes formed, log K, from 5.07 to 5.36. Organic matter-quality related characteristics had little influence on Cu adsorption in acid soils, especially if compared with pH, the degree of Cu saturation and the amount of soil organic matter. - The effect of organic matter quality on Cu adsorption in acid soils was low compared with other soil characteristics such as pH or degree of Cu saturation.

Complete and Partial Photo-oxidation of Dissolved Organic Matter Draining Permafrost Soils.

Science.gov (United States)

Ward, Collin P; Cory, Rose M

2016-04-05

Photochemical degradation of dissolved organic matter (DOM) to carbon dioxide (CO2) and partially oxidized compounds is an important component of the carbon cycle in the Arctic. Thawing permafrost soils will change the chemical composition of DOM exported to arctic surface waters, but the molecular controls on DOM photodegradation remain poorly understood, making it difficult to predict how inputs of thawing permafrost DOM may alter its photodegradation. To address this knowledge gap, we quantified the susceptibility of DOM draining the shallow organic mat and the deeper permafrost layer of arctic soils to complete and partial photo-oxidation and investigated changes in the chemical composition of each DOM source following sunlight exposure. Permafrost and organic mat DOM had similar lability to photomineralization despite substantial differences in initial chemical composition. Concurrent losses of carboxyl moieties and shifts in chemical composition during photodegradation indicated that photodecarboxylation could account for 40-90% of DOM photomineralized to CO2. Permafrost DOM had a higher susceptibility to partial photo-oxidation compared to organic mat DOM, potentially due to a lower abundance of phenolic moieties with antioxidant properties. These results suggest that photodegradation will likely continue to be an important control on DOM fate in arctic freshwaters as the climate warms and permafrost soils thaw.

Organic matter dynamics and N mineralization in grassland soils

OpenAIRE

Hassink, J.

1995-01-01

The aims of this study are i) to improve our understanding of the interactions between soil texturelsoil structure, soil organic matter, soil biota and mineralization in grassland soils, ii) to develop a procedure that yields soil organic matter fractions that can be determined directly and can be used in soil organic matter models, iii) to develop a model that predicts the long-term dynamics of soil organic matter, iv) to develop a simple model that can be used by farmers and advi...

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.

Cycling downwards - dissolved organic matter in soils

NARCIS (Netherlands)

Kaiser, K.; Kalbitz, K.

2012-01-01

Dissolved organic matter has been recognized as mobile, thus crucial to translocation of metals, pollutants but also of nutrients in soil. We present a conceptual model of the vertical movement of dissolved organic matter with soil water, which deviates from the view of a chromatographic stripping

Distribution of transformed organic matter in structural units of loamy sandy soddy-podzolic soil

Science.gov (United States)

Kogut, B. M.; Yashin, M. A.; Semenov, V. M.; Avdeeva, T. N.; Markina, L. G.; Lukin, S. M.; Tarasov, S. I.

2016-01-01

The effect of land use types and fertilizing systems on the structural and aggregate composition of loamy sandy soddy-podzolic soil and the quantitative parameters of soil organic matter has been studied. The contribution of soil aggregates 2-1 mm in size to the total Corg reserve in the humus horizon is higher than the contributions of other aggregates by 1.3-4.2 times. Reliable correlations have been revealed between the contents of total (Corg), labile (Clab), and active (C0) organic matter in the soil. The proportion of C0 is 44-70% of Clab extractable by neutral sodium pyrophosphate solution. The contributions of each of the 2-1, 0.5-0.25, and fractions to the total C0 reserve are 14-21%; the contributions of each of the other fractions are 4-12%. The chemically labile and biologically active components of humic substances reflect the quality changes of soil organic matter under agrogenic impacts. A conceptual scheme has been proposed for the subdivision of soil organic matter into the active, slow (intermediate), and passive pools. In the humus horizon of loamy sandy soddy-podzolic soil, the active, slow, and passive pools contain 6-11, 34-65, and 26-94% of the total Corg, respectively.

Clay-associated organic matter in kaolinitic and smectitic soils

NARCIS (Netherlands)

Wattel-Koekkoek, E.J.W.

2002-01-01

The primary source of soil organic matter is plant debris of all kinds, such as dead roots, leaves and branches that enter into the soil and are then biologically decomposed at variable rates. Organic matter has many different important functions on a local and global scale. Soil organic matter is

The molecular structure of the insoluble organic matter isolated from Murchison carbonaceous chondrite.

Science.gov (United States)

Robert, F.; Derenne, S.

2009-04-01

During these last 10 years, our group has characterized the various molecular moieties of the insoluble organic matter (IOM) isolated from carbonaceous meteorites with the aim of reconstructing its overall molecular structure. Indeed, a precise knowledge of the structure of an organic macromolecule contains irreplaceable information that traces its mechanisms of synthesis and its conditions of formation. Such a modelled structure will be presented. Carbonaceous chondrites contain up to 3 wt % of carbon that is under the form of soluble and insoluble fractions. The IOM, which constitutes more than 75 wt% of the bulk organic matter, was isolated from the bulk rock through successive acid dissolutions. The chemical structure of the isolated IOM has been studied by both (1) destructive and (2) non destructive methods. Methods include thermal and chemical degradations followed by GC/MS, spectroscopic techniques (nuclear magnetic resonance, Fourier transform infra red spectroscopy; X-ray absorption near-edge spectroscopy, electron paramagnetic resonance) along with high resolution transmission electron microscopy. Although each technique alone cannot provide definite information on the chemical structure of such a complex material, the combination of the results can be used to reconstruct the molecular structure of the IOM. The proposed structure accounts for all these measured parameters. The details of this structure reveal information of the conditions of its formation in space and allow to discuss the mechanisms of organo-synthesis in the cosmochemical context of the formation of the solar system.

Biologically Active Organic Matter in Soils of European Russia

Science.gov (United States)

Semenov, V. M.; Kogut, B. M.; Zinyakova, N. B.; Masyutenko, N. P.; Malyukova, L. S.; Lebedeva, T. N.; Tulina, A. S.

2018-04-01

Experimental and literature data on the contents and stocks of active organic matter in 200 soil samples from the forest-tundra, southern-taiga, deciduous-forest, forest-steppe, dry-steppe, semidesert, and subtropical zones have been generalized. Natural lands, agrocenoses, treatments of long-term field experiments (bare fallow, unfertilized and fertilized crop rotations, perennial plantations), and different layers of soil profile are presented. Sphagnum peat and humus-peat soil in the tundra and forest-tundra zones are characterized by a very high content of active organic matter (300-600 mg C/100 g). Among the zonal soils, the content of active organic matter increases from the medium (75-150 mg C/100 g) to the high (150-300 mg C/100 g) level when going from soddy-podzolic soil to gray forest and dark-gray forest soils and then to leached chernozem. In the series from typical chernozem to ordinary and southern chernozem and chestnut and brown semidesert soils, a decrease in the content of active organic matter to the low (35-75 mg C/100 g) and very low (organic matter. Most arable soils are mainly characterized by low or very low contents of active organic matter. In the upper layers of soils, active organic matter makes up 1.2-11.1% of total Corg. The profile distribution of active organic matter in the studied soils coincides with that of Corg: their contents appreciably decrease with depth, except for brown semidesert soil. The stocks of active organic matter vary from 0.4 to 5.4 t/ha in the layer of 0-20 cm and from 1.0 to 12.4/ha in the layer of 0-50 cm of different soil types.

Structure and organic matter under different soil management conditions in the center of Argentina

International Nuclear Information System (INIS)

Bricchi, E.

2004-01-01

In Central Argentina, Cordoba Province, as in different parts of the world, the equilibrium state of soil under natural condition has been modified by both the replacement of natural vegetation and by tillage. With time, these two disturbing factors have led to a new soil state whose main characteristic is an important decrease of chemical, physical and biological soil functions. The degree of these changes is directly related to soil resistance according to soil genesis. The soil organic matter and the structure of the superficial profile of soil are suitable indicators mainly for physical functions. Recently, it became necessary to look for a combination of technologies leading to an energy input throughout conservation tillage systems, soil covering and agro-chemicals which tend to improve soil quality in order to obtain a sustainable production. The removal of natural vegetation and tillage systems have caused the following effects on the first centimetres of soils: A 77 to 80% loss of organic matter during a period of about 80 years. Changes in the water stable aggregates distribution. A 77% loss of large aggregates and a 55% gain of fine aggregates. Our results would indicate that the disturbance level was higher to the natural resistance of soil. The organic carbon content in the first centimetres of soil is increased when all crop stubble remains on the field and conservationist tillage is applied. Conservation tillages are more efficient in the lower position of relief, meaning the beginning of a change of organic matter tendency that would possibly tend to new equilibrium state. On the other hand, the percentage of water stable aggregates would also be increased as consequence of a higher organic carbon content

Determination of organic products resulting of chemical and radiochemical decompositions of bitumen. Applications to embedded bitumens

International Nuclear Information System (INIS)

Walczak, I.

2000-01-01

Bitumen can be used for embedding most of wastes because of its high impermeability and its relatively low reactivity with of chemicals. Bituminization is one of selected solutions in agreement with nuclear safety, waste compatibility and economic criteria. Bitumen, during storage, undergoes an auto-irradiation due to embedded radio-elements. During this stage,drums are not airtight then oxygen is present. In disposal configuration, water, which is a potential vector of radioactivity and organic matter, is an other hazard factor liable to deteriorate the containment characteristics of bitumen wastes. The generation of water-soluble organic complexing agents can affect the integrity of the wasteform due to an increase of the radionuclides solubility. The first aim of this work is the quantitative and qualitative characterisation of soluble organic matter in bitumen leachates. Different leaching solutions were tested (various pH, ionic strength, ratio S/V). When the pH of the leaching solutions increases, the total organic carbon released increases as well. Identified molecules are aromatics like naphthalene, oxidised compounds like alcohols, linear carbonyls, aromatics, glycols and nitrogen compounds. For the cement equilibrated solution (pH 13.5), the effect of ionic strength becomes significative and influences the release of soluble organic matter. This soluble organic matter can be bio-degraded if microorganisms can growth. The second aim of this work is to study the effect of radio-oxidative ageing on the bitumen confinement properties. During radio-oxidation, the chemical properties of bitumen are modified. The μ-IRTF analysis shows the formation of hydroxyl compounds and aromatic acids. The formation of these polar groups does not influence in our study the water uptake. However the organic matter release increases significantly with the irradiation dose. (author)

Investigation of water-soluble organic matter extracted from shales during leaching experiments

Science.gov (United States)

Zhu, Yaling; Vieth-Hillebrand, Andrea; Wilke, Franziska D. H.; Horsfield, Brian

2017-04-01

The huge volumes and unknown composition of flowback and produced waters cause major public concerns about the environmental and social compatibility of hydraulic fracturing and the exploitation of gas from unconventional reservoirs. Flowback and produced waters contain not only residues of fracking additives but also chemical species that are dissolved from the shales themselves during fluid-rock interaction. Knowledge of the composition, size and structure of dissolved organic carbon (DOC) as well as the main controls on the release of DOC are a prerequisite for a better understanding of these interactions and its effects on composition of flowback and produced water. Black shales from four different geological settings and covering a maturity range Ro = 0.3-2.6% were extracted with deionized water. The DOC yields were found to decrease rapidly with increasing diagenesis and remain low throughout catagenesis. Four DOC fractions have been qualitatively and quantitatively characterized using size-exclusion chromatography. The concentrations of individual low molecular weight organic acids (LMWOA) decrease with increasing maturity of the samples except for acetate extracted from the overmature Posidonia shale, which was influenced by hydrothermal brines. The oxygen content of the shale organic matter also shows a significant influence on the release of organic acids, which is indicated by the positive trend between oxygen index (OI) and the concentrations of formate and acetate. Based on our experiments, both the properties of the organic matter source and the thermal maturation progress of the shale organic matter significantly influence the amount and quality of extracted organic compounds during the leaching experiments.

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.

Organic speciation of size-segregated atmospheric particulate matter

Science.gov (United States)

Tremblay, Raphael

Particle size and composition are key factors controlling the impacts of particulate matter (PM) on human health and the environment. A comprehensive method to characterize size-segregated PM organic content was developed, and evaluated during two field campaigns. Size-segregated particles were collected using a cascade impactor (Micro-Orifice Uniform Deposit Impactor) and a PM2.5 large volume sampler. A series of alkanes and polycyclic aromatic hydrocarbons (PAHs) were solvent extracted and quantified using a gas chromatograph coupled with a mass spectrometer (GC/MS). Large volume injections were performed using a programmable temperature vaporization (PTV) inlet to lower detection limits. The developed analysis method was evaluated during the 2001 and 2002 Intercomparison Exercise Program on Organic Contaminants in PM2.5 Air Particulate Matter led by the US National Institute of Standards and Technology (NIST). Ambient samples were collected in May 2002 as part of the Tampa Bay Regional Atmospheric Chemistry Experiment (BRACE) in Florida, USA and in July and August 2004 as part of the New England Air Quality Study - Intercontinental Transport and Chemical Transformation (NEAQS - ITCT) in New Hampshire, USA. Morphology of the collected particles was studied using scanning electron microscopy (SEM). Smaller particles (one micrometer or less) appeared to consist of solid cores surrounded by a liquid layer which is consistent with combustion particles and also possibly with particles formed and/or coated by secondary material like sulfate, nitrate and secondary organic aerosols. Source apportionment studies demonstrated the importance of stationary sources on the organic particulate matter observed at these two rural sites. Coal burning and biomass burning were found to be responsible for a large part of the observed PAHs during the field campaigns. Most of the measured PAHs were concentrated in particles smaller than one micrometer and linked to combustion sources

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.

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)

A new method for identifying the types of organic matter

International Nuclear Information System (INIS)

Tong Chunhan; Li Guodong

1991-01-01

A new method for dividing the types of organic matter according to V and Ni contents in soluble organic matter determined by NAA is introduced. The research site was an oil-gas field in northeastern China. The type of organic matter is an important parameter in evaluating an oil or a gas field. The conventional organic geochemistry methods will meet unsurmountable difficulties when the maturity of organic matter is high. The method described in this paper can solve the problem. (author) 4 refs.; 1 fig.; 2 tabs

Chemical cleaning-associated generation of dissolved organic matter and halogenated byproducts in ceramic MBR: Ozone versus hypochlorite.

Science.gov (United States)

Sun, Huifang; Liu, Hang; Han, Jiarui; Zhang, Xiangru; Cheng, Fangqin; Liu, Yu

2018-04-24

This study characterized the dissolved organic matter (DOM) and byproducts generated after the exposure of activated sludge to ozone and NaClO in ceramic MBR. It was found that NaClO triggered more significant release of DOM than ozone. Proteins with the molecular weight greater than 20 kDa and humic acid like-substances were the principal components of DOM generated by NaClO, while ozone was found to effectively degrade larger biopolymers to low molecular weight substances. The results showed that more than 80% of DOM generated by NaClO and ozone could pass through the 0.2-μm ceramic membrane. Furthermore, total organic chlorine (TOCl) was determined to be the principal species of halogenated byproducts in both cases, while the generation of TOCl by NaClO was much more significant than that by ozone. Only a small fraction of TOCl was removed by the 0.2-μm ceramic membrane. More importantly, the toxic bioassays further revealed that the supernatant of sludge suspension and permeate in the MBR with NaClO cleaning exhibited higher developmental toxicity to the polychaete embryos than those by ozone. The results clearly showed that on-line chemical cleaning with ozone should be a more eco-friendly and safer approach for sustaining long-term membrane permeability in ceramic MBR. Copyright © 2018 Elsevier Ltd. All rights reserved.

Influence of chlorothalonil on the removal of organic matter in horizontal subsurface flow constructed wetlands.

Science.gov (United States)

Casas-Zapata, Juan C; Ríos, Karina; Florville-Alejandre, Tomás R; Morató, Jordi; Peñuela, Gustavo

2013-01-01

This study investigates the effects of chlorothalonil (CLT) on chemical oxygen demand (COD) and dissolved organic carbon (DOC) in pilot-scale horizontal subsurface flow constructed wetlands (HSSFCW) planted with Phragmites australis. Physicochemical parameters of influent and effluent water samples, microbial population counting methods and statistical analysis were used to evaluate the influence of CLT on organic matter removal efficiency. The experiments were conducted on four planted replicate wetlands (HSSFCW-Pa) and one unplanted control wetland (HSSFCW-NPa). The wetlands exhibited high average organic matter removal efficiencies (HSSFCW-Pa: 80.6% DOC, 98.0% COD; HSSFCW-NPa: 93.2% DOC, 98.4% COD). The addition of CLT did not influence organic removal parameters. In all cases CLT concentrations in the effluent occurred in concentrations lower than the detection limit of the analytical method. Microbial population counts from HSSFCW-Pa showed significant correlations among different microbial groups and with different physicochemical variables. The apparent independence of organic matter removal and CLT inputs, along with the CLT depletion observed in effluent samples demonstrated that HSSFCW are a viable technology for the treatment of agricultural effluents contaminated with organo-chloride pesticides like CLT.

Including chemical-related impact categories in LCA on printed matter does it matter?

DEFF Research Database (Denmark)

Larsen, Henrik Fred; Hansen, Morten Søes; Hauschild, Michael Zwicky

2004-01-01

global warming, acidification and nutrification. The studies focus on energy consumption including the emissions and impact categories related to energy. The chemical-related impact categories comprising ecotoxicity and human toxicity are not included at all or only to a limited degree. In this paper we...... include these chemical-related impact categories by making use of some of the newest knowledge about emissions from the production at the printing industry combined with knowledge about the composition of the printing materials used during the production of offset printed matter. This paper is based...... printed matter produced on a fictitious sheet feed offset printing industry in Europe has been identified and shown in Figure 1 (light bars). „Ï The effect of including the chemical related impact categories is substantial as shown in Figure 1, e.g. the importance of paper is reduced from 67% to 31...

Global chemical composition of ambient fine particulate matter for exposure assessment.

Science.gov (United States)

Philip, Sajeev; Martin, Randall V; van Donkelaar, Aaron; Lo, Jason Wai-Ho; Wang, Yuxuan; Chen, Dan; Zhang, Lin; Kasibhatla, Prasad S; Wang, Siwen; Zhang, Qiang; Lu, Zifeng; Streets, David G; Bittman, Shabtai; Macdonald, Douglas J

2014-11-18

Epidemiologic and health impact studies are inhibited by the paucity of global, long-term measurements of the chemical composition of fine particulate matter. We inferred PM2.5 chemical composition at 0.1° × 0.1° spatial resolution for 2004-2008 by combining aerosol optical depth retrieved from the MODIS and MISR satellite instruments, with coincident profile and composition information from the GEOS-Chem global chemical transport model. Evaluation of the satellite-model PM2.5 composition data set with North American in situ measurements indicated significant spatial agreement for secondary inorganic aerosol, particulate organic mass, black carbon, mineral dust, and sea salt. We found that global population-weighted PM2.5 concentrations were dominated by particulate organic mass (11.9 ± 7.3 μg/m(3)), secondary inorganic aerosol (11.1 ± 5.0 μg/m(3)), and mineral dust (11.1 ± 7.9 μg/m(3)). Secondary inorganic PM2.5 concentrations exceeded 30 μg/m(3) over East China. Sensitivity simulations suggested that population-weighted ambient PM2.5 from biofuel burning (11 μg/m(3)) could be almost as large as from fossil fuel combustion sources (17 μg/m(3)). These estimates offer information about global population exposure to the chemical components and sources of PM2.5.

Organic matter in primitive meteorites: a study of the hydrogen isotopic distribution in CM-type carbonaceous chondrites

Science.gov (United States)

Piani, L.; Yurimoto, H.; Remusat, L.; Gonzales, A.; Marty, B.

2017-12-01

Chondrite meteorites are fragments of rocks coming from small bodies of the asteroid belt and constitute witnesses of the volatile-rich reservoirs present in the inner protoplanetary disk. Among these meteorites, carbonaceous chondrites contain the largest quantity of water and organic matter and are one of the most probable candidates for the delivery of water and molecular origin of life to Earth. Organic matter in carbonaceous chondrites is intimately mixed with hydrated minerals challenging its in situ characterization and the determination of its H-isotope composition (Le Guillou et al., GCA 131, 2014). Organic matter occurs as soluble components (in water or organic solvents) and an insoluble macromolecule. The insoluble organic matter (IOM) is efficiently isolated after acid leaching of the chondrite minerals. IOM has thus been investigated by a large set of analytical techniques allowing its structural organization, chemical composition and isotopic composition to be determined at several scales (e.g. Derenne and Robert, MAPS 45, 2010). In the soluble counterpart (SOM), targeted studies have shown large ranges of D/H ratios in the different classes of soluble organic compounds (i.e. carboxylic acids, ketones and aldehydes, amino-acids etc.) (Remusat, Planetary Mineralogy 15, 2015 and references therein). This D/H distribution indicates a complex and probably multiple-stage synthesis of this organic compounds occurring at different stages of the disk evolution. Nevertheless, inventories of the known C-bearing species in carbonaceous chondrites (carbonates, SOM and IOM) show that about 40-50 % of the carbon is hidden within the matrix (Alexander et al., MAPS 50, 2015). In this study, we perform in situ hydrogen isotope analyses at the micrometer scale by secondary ion mass spectrometry to investigate the distribution of organic matter in primitive chondrites without the use of any chemical treatment. Correlated analyses of the D/H and C/H ratios allow us to

Mitigation of algal organic matter released from Chaetoceros affinis and Hymenomonas by in situ generated ferrate

KAUST Repository

Deka, Bhaskar Jyoti; Jeong, Sanghyun; AlizadehTabatabai, S.Assiyeh; An, Alicia Kyoungjin

2018-01-01

This study demonstrates the application of in situ ferrate (Fe(VI)) for the efficient removal of dissolved algal organic matter (AOM) from seawater. Sodium hypochlorite (NaOCl) and ferric (Fe(III)) were used to produce in situ Fe(VI) by wet chemical

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

How soil organic matter composition controls hexachlorobenzene-soil-interactions: adsorption isotherms and quantum chemical modeling.

Science.gov (United States)

Ahmed, Ashour A; Kühn, Oliver; Aziz, Saadullah G; Hilal, Rifaat H; Leinweber, Peter

2014-04-01

Hazardous persistent organic pollutants (POPs) interact in soil with the soil organic matter (SOM) but this interaction is insufficiently understood at the molecular level. We investigated the adsorption of hexachlorobenzene (HCB) on soil samples with systematically modified SOM. These samples included the original soil, the soil modified by adding a hot water extract (HWE) fraction (soil+3 HWE and soil+6 HWE), and the pyrolyzed soil. The SOM contents increased in the order pyrolyzed soilsoilsoil+3 HWEsoil+6 HWE. For the latter three samples this order was also valid for the HCB adsorption. The pyrolyzed soil adsorbed more HCB than the other samples at low initial concentrations, but at higher concentrations the HCB adsorption became weaker than in the samples with HWE addition. This adsorption combined with the differences in the chemical composition between the soil samples suggested that alkylated aromatic, phenol, and lignin monomer compounds contributed most to the HCB adsorption. To obtain a molecular level understanding, a test set has been developed on the basis of elemental analysis which comprises 32 representative soil constituents. The calculated binding energy for HCB with each representative system shows that HCB binds to SOM stronger than to soil minerals. For SOM, HCB binds to alkylated aromatic, phenols, lignin monomers, and hydrophobic aliphatic compounds stronger than to polar aliphatic compounds confirming the above adsorption isotherms. Moreover, quantitative structure-activity relationship (QSAR) of the binding energy with independent physical properties of the test set systems for the first time indicated that the polarizability, the partial charge on the carbon atoms, and the molar volume are the most important properties controlling HCB-SOM interactions. Copyright © 2013 Elsevier B.V. All rights reserved.

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

Here, organic matter is a complex material that represents the long-term decay products from plants and other organisms in the soil. When organic matter is allowed to build up in a soil, the soil color at the surface usually turns a darker color, often with a red or brown hue. Typically in Florida mineral soils, organic matter content is quite low, within the range of 1 to 5%. However, in some soils that remain flooded for most of the year, organic matter can build up with time and actually become the soil. Such is the case for the organic soils, or histosols, found in southern Florida. These organic soils comprise much of the Water Conservation Areas, Everglades National Park (ENP), Big Cypress Basin, and the Everglades Agricultural Area (EAA). It is important to document organic matter accumulation in the Everglades to gauge the effectiveness of wetland creation and succession. For the EAA, the drained soils lose organic matter due to oxidation, so measurement of the organic matter content of these soils over the course of time indicates the oxidation potential and mineral incorporation from bedrock. Due to the wide diversity of soil types and methods of measuring soil organic matter, there is a need to devise a more universal method applicable to many types of histosols in south Florida. The intent of this publication is: 1.To describe a simple laboratory method for determining the organic matter content of the organic soils of southern Florida and demonstrate the importance of using this new procedure for improved accuracy and precision; 2.To utilize this updated laboratory procedure for field sites across Everglades wetlands and the EAA; and 3. To recommend this procedure be used by growers, state and federal agencies, and university and agency researchers dealing with the management of organic soils in southern Florida. Growers can use this improvement to organic matter measurement to keep lab testing costs low while getting a better, more quantitative

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.

Soil organic matter dynamics and the global carbon cycle

International Nuclear Information System (INIS)

Post, W.M.; Emanuel, W.R.; King, A.W.

1992-01-01

The large size and potentially long residence time of the soil organic matter pool make it an important component of the global carbon cycle. Net terrestrial primary production of about 60 Pg C·yr -1 is, over a several-year period of time, balanced by an equivalent flux of litter production and subsequent decomposition of detritus and soil organic matter. We will review many of the major factors that influence soil organic matter dynamics that need to be explicitly considered in development of global estimates of carbon turnover in the world's soils. We will also discuss current decomposition models that are general enough to be used to develop a representation of global soil organic matter dynamics

Organic matter of subsoil horizons under broadleaved forest: Highly processed or labile and plant-derived?

NARCIS (Netherlands)

Vancampenhout, K.; Vos, de B.; Wouters, K.; Swennen, R.; Buurman, P.

2012-01-01

Between 30 and 63% of the soil organic matter (SOM) is stored below 30 cm, making subsoil-SOM an important source and sink in the global carbon cycle. Nevertheless, detailed information on the composition of subsoil-SOM remains scarce. This study aims to evaluate the chemical composition of SOM in

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%).

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

Development and evaluation of a radial anaerobic/aerobic reactor treating organic matter and nitrogen in sewage

Directory of Open Access Journals (Sweden)

L. H. P. Garbossa

2005-12-01

Full Text Available The design and performance of a radial anaerobic/aerobic immobilized biomass (RAAIB reactor operating to remove organic matter, solids and nitrogen from sewage are discussed. The bench-scale RAAIB was divided into five concentric chambers. The second and fourth chambers were packed with polyurethane foam matrices. The performance of the reactor in removing organic matter and producing nitrified effluent was good, and its configuration favored the transfer of oxygen to the liquid mass due to its characteristics and the fixed polyurethane foam bed arrangement in concentric chambers. Partial denitrification of the liquid also took place in the RAAIB. The reactor achieved an organic matter removal efficiency of 84%, expressed as chemical oxygen demand (COD, and a total Kjeldahl nitrogen (TKN removal efficiency of 96%. Average COD, nitrite and nitrate values for the final effluent were 54 mg.L-1, 0.3 mg.L-1 and 22.1 mg.L-1, respectively.

The method for determination of parameters of the phenomenological continual model of soil organic matter transformation

Directory of Open Access Journals (Sweden)

S. I. Bartsev

2015-06-01

Full Text Available A possible method for experimental determination of parameters of the previously proposed continual mathematical model of soil organic matter transformation is theoretically considered in this paper. The previously proposed by the authors continual model of soil organic matter transformation, based on using the rate of matter transformation as a continual scale of its recalcitrance, describes the transformation process phenomenologically without going into detail of microbiological mechanisms of transformation. Thereby simplicity of the model is achieved. The model is represented in form of one differential equation in first­order partial derivatives, which has an analytical solution in elementary functions. The model equation contains a small number of empirical parameters which generally characterize environmental conditions where the matter transformation process occurs and initial properties of the plant litter. Given the values of these parameters, it is possible to calculate dynamics of soil organic matter stocks and its distribution over transformation rate. In the present study, possible approaches for determination of the model parameters are considered and a simple method of their experimental measurement is proposed. An experiment of an incubation of chemically homogeneous samples in soil and multiple sequential measurement of the sample mass loss with time is proposed. An equation of time dynamics of mass loss of incubated homogeneous sample is derived from the basic assumption of the presented soil organic matter transformation model. Thus, fitting by the least squares method the parameters of sample mass loss curve calculated according the proposed mass loss dynamics equation allows to determine the parameters of the general equation of soil organic transformation model.

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

Exploring the Contribution of Primary Marine Organic Matter to the Arctic Boundary Layer

Science.gov (United States)

Collins, D. B.; Chang, R. Y. W.; Boyer, M.; Abbatt, J.

2016-12-01

The ocean is a significant source of aerosol to the atmosphere, and contributes significantly to the aerosol population especially in remote locations. Both primary and secondary processes connect the ocean to ambient aerosol loadings, but the extent to which the ocean is a source of organic material to the atmosphere is a current topic of scientific debate. The contribution of primary marine aerosol to atmospheric organic matter may have an influence on the water uptake properties and chemical reactivity of primary marine aerosol particles, influencing their climate-relevant properties. In this study, we characterize the contribution of primary marine aerosol to the arctic marine boundary layer using coincident quantitative measurements of freshly-produced sea spray aerosol and ambient marine aerosol to the arctic boundary layer during an expedition aboard the CCGS Amundsen. Sea spray production experiments were conducted during the cruise using a tank fitted with a plunging waterfall apparatus, a technique which has been recently shown to closely mimic the aerosol production behavior of controlled breaking waves. Comparison of the chemical composition of sea spray particles generated from water samples in various locations throughout the Canadian Archipelago will be presented. A tracer analysis of specific compounds known to be important contributors to primary marine organic material are tracked using GC/MS, along with those known to be tracers of biological aerosol and other organic matter sources. Size-segregated trends in tracer concentrations and ratios with inorganic components will be discussed in the context of understanding the contribution of primary organics to the Arctic atmosphere and in comparison with other sources of organic material observed during the ship-board campaign.

Sterilization affects soil organic matter chemistry and bioaccumulation of spiked p,p'-DDE and anthracene by earthworms

Energy Technology Data Exchange (ETDEWEB)

Kelsey, Jason W., E-mail: kelsey@muhlenberg.ed [Program in Environmental Science and Department of Chemistry, Muhlenberg College, 2400 Chew Street, Allentown, PA 18104 (United States); Slizovskiy, Ilya B.; Peters, Richard D.; Melnick, Adam M. [Program in Environmental Science and Department of Chemistry, Muhlenberg College, 2400 Chew Street, Allentown, PA 18104 (United States)

2010-06-15

Laboratory experiments were conducted to assess the effects of soil sterilization on the bioavailability of spiked p,p'-DDE and anthracene to the earthworms Eisenia fetida and Lumbricus terrestris. Physical and chemical changes to soil organic matter (SOM) induced by sterilization were also studied. Uptake of both compounds added after soil was autoclaved or gamma irradiated increased for E. fetida. Sterilization had no effect on bioaccumulation of p,p'-DDE by L. terrestris, and anthracene uptake increased only in gamma-irradiated soils. Analyses by FT-IR and DSC indicate sterilization alters SOM chemistry and may reduce pollutant sorption. Chemical changes to SOM were tentatively linked to changes in bioaccumulation, although the effects were compound and species specific. Artifacts produced by sterilization could lead to inaccurate risk assessments of contaminated sites if assumptions derived from studies carried out in sterilized soil are used. Ultimately, knowledge of SOM chemistry could aid predictions of bioaccumulation of organic pollutants. - Soil sterilization affects soil organic matter chemistry and pollutant bioaccumulation.

Photochemical Reactions of Particulate Organic Matter: Deciphering the Role of Direct and Indirect Processes

Science.gov (United States)

Carrasquillo, A. J.; Gelfond, C. E.; Kocar, B. D.

2016-12-01

Photochemical reactions of natural organic matter (NOM) represent potentially important pathways for biologically recalcitrant material to be chemically altered in aquatic systems. Irradiation can alter the physical state of organic matter by facilitating the cycling between the particulate (POM) and dissolved (DOM) pools, however, a molecular level understanding of this chemically dynamic system is currently lacking. Photochemical reactions of a target molecule proceed by the direct absorption of a photon, or through reaction with a second photolytically generated species (i.e. the hydroxyl radical, singlet oxygen, excited triplet state NOM, hydrogen peroxide, etc.). Here, we isolate the major direct and indirect photochemical reactions of a lignocellulose-rich POM material (Phragmites australis) to determine their relative importance in changing the the chemical structure of the parent POM, and in the production of DOM. We measured POM molecular structure using a combination of NMR and FTIR for bulk analyses and scanning transmission x-ray microscopy (STXM) for spatially resolved chemistry, while the chemical composition of photo-produced DOM was measured using ultra-high resolution mass spectrometry. Results are discussed in the context of the differences in chemical composition of both NOM pools resulting from the isolated photochemical pathways. All treatments result in an increase in DOM with reaction time, indicating that the larger POM matrix is likely fragmenting into smaller more soluble species. Spectroscopic measurements, on the other hand, point to functionalization reactions which increase the abundance of alcohol, acid, and carbonyl moieties in both carbon pools. This unique dataset provides new insight into how photochemical reactions alter the chemical composition of NOM while highlighting the relative importance of indirect pathways.

Relationship between Mineral and Organic Matter in Shales: The Case of Shahejie Formation, Dongying Sag, China

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Xiang Zeng

2018-05-01

Full Text Available Types of organic matter and mineral associations and microstructures of shales can reflect the depositional mechanism and sedimentary environment. Therefore, analysis of organic matter and mineral associations is a prerequisite for research on fine-grained sedimentary rocks. Shales from the Eocene Shahejie Formation in the Dongying Sag of China were selected to classify their lithofacies and to investigate the characteristics of their organic matter and mineral associations. This analysis identified six lithofacies (e.g., laminated shales and massive mudstones; in all the lithofacies, clay minerals exhibit a positive correlation with detrital minerals, thus indicating that they were derived from the same source. The comprehensive analysis of mineral and organic matter associations reveals that detrital minerals were deposited with low-hydrogen index (HI OM. The deposition of detrital minerals was mainly a physical process. Clay minerals can undergo deposition in one of two ways due to their surface charge: they can either aggregate with high-HI OM via chemical deposition, thus forming organic-rich laminae, or they can be deposited together with low-HI OM via physical deposition, thus forming clay-rich laminae or a massive matrix. Carbonate minerals, which often coexist with high-HI OM, are biological sediments. The analysis of the sedimentary characteristics of these organic matter and mineral associations indicates that the sedimentary processes differ between various lithofacies: e.g., the discontinuous laminated shale represents the product of biophysical processes. Differences in depositional mechanisms are also present in each sub-member. Therefore, it is important to analyze the properties of minerals and organic matter, as well as their associations, to more deeply understand the classification of lithofacies and the depositional processes of shales and mudstones.

Organic Matter Dynamics in Soils Regenerating from Degraded ...

African Journals Online (AJOL)

The area of secondary forest (SF) regenerating from degraded abandoned rubber (Hevea brasiliensis) plantation is increasing in the rainforest zone of south southern Nigeria; however, the build-up of soil organic matter following abandonment is not well understood. This study examined the build-up of soil organic matter in ...

Analytic study of organic matters in Lodeve uranium ore

International Nuclear Information System (INIS)

Campuzano, E.J.

1981-01-01

Exploitation of uranium in the Permian basin of Lodeve is difficult because of simultaneous extraction of organic matters which are found, in small proportion, in ammonium diuranate and a supplementary purification is required. Available information on natural organic matters are briefly reviewed. Natural organic matters contained in the Lodeve uranium ore processing fluid is separated and fractionated. Physicochemical properties of ligands in each fraction are studied. The existence of bonds between these ligands and dissolved uranium is experimentally demonstrated [fr

Soil organic matter chemistry changes upon secondary succession in Imperata Grasslands , Indonesia: A pyrolysis - GC/MS study

NARCIS (Netherlands)

Yassir, I.; Buurman, P.

2012-01-01

The chemical composition of soil organic matter (SOM) following secondary succession in Imperata grassland was investigated by Pyrolysis-Gas Chromatography/Mass Spectrometry (GC/MS). We studied 46 samples from different stages of succession using plots that last burned 3 and 9 years previously,

Repeated applications of compost and manure mainly affect the size and chemical nature of particulate organic matter in a loamy soil after 8 years

Science.gov (United States)

Peltre, Clement; Dignac, Marie-France; Doublet, Jeremy; Plante, Alain; Houot, Sabine

2013-04-01

Land application of exogenous organic matter (EOM) of residual origin can help to maintain or increase soil organic carbon (SOC) stocks. However, it remains necessary to quantify and predict the soil C accumulation and to determine under which form the C accumulates. Changes to the chemical composition of soil organic matter (SOM) after repeated applications of composts and farmyard manure were investigated in a field experiment (Qualiagro experiment, Ile-de-France) after 8 years of applications of green waste and sludge compost (GWS), municipal solid waste compost (MSW), biowaste compost (BIOW) or farmyard manure (FYM). The soil was fractionated into particulate organic matter >50 µm (POM), a heavy fraction >50 µm and a 0-50 µm fraction demineralized with hydrofluoric acid (HF). Repeated EOM applications significantly increased total SOC stocks, the C amount in the POM fraction and to a less extent in the 0-50 µm fraction compared to the reference treatment. Compost applications accumulated C preferentially under the form of coarse organic matter of size >50 µm, whereas the FYM accumulated similar C proportions of size >50 µm and 0-50 µm, which was attributed to the presence in the FYM of a fraction of labile C stimulating microbial activity and producing humified by-products together with a fraction of stabilized C directly alimenting the humified fraction of SOC. Pyrolysis-GC/MS and DRIFT spectroscopy revealed enrichment in lignin in the POM fractions of amended soils with GWS, BIOW and FYM. In the soil receiving MSW compost, the pyrolysate of the POM fraction revealed the presence of plastics originating from the MSW compost. A lower C mineralization during laboratory incubation was found for the POM fractions of amended soils compared with the POM from reference soil. This feature was related to a lower ratio of (furfural+acetic acid) / pyrole pyrolysis products in POM of amended vs. reference plots, indicating a higher degree of recalcitrance.. The POM

Effect of influent aeration on removal of organic matter from coffee processing wastewater in constructed wetlands.

Science.gov (United States)

Rossmann, Maike; Matos, Antonio Teixeira; Abreu, Edgar Carneiro; Silva, Fabyano Fonseca; Borges, Alisson Carraro

2013-10-15

The aim of the present study was to evaluate the influence of aeration and vegetation on the removal of organic matter in coffee processing wastewater (CPW) treated in 4 constructed wetlands (CWs), characterized as follows: (i) ryegrass (Lolium multiflorum) cultivated system operating with an aerated influent; (ii) non-cultivated system operating with an aerated influent, (iii) ryegrass cultivated system operating with a non-aerated influent; and (iv) non-cultivated system operating with a non-aerated influent. The lowest average chemical oxygen demand (COD), biochemical oxygen demand (BOD) and total suspended solids (TSS) removal efficiencies of 87, 84 and 73%, respectively, were obtained in the ryegrass cultivated system operating with a non-aerated influent. However, ryegrass cultivation did not influence the removal efficiency of organic matter. Artificial aeration of the CPW, prior to its injection in the CW, did not improve the removal efficiencies of organic matter. On other hand it did contribute to increase the instantaneous rate at which the maximum COD removal efficiency was reached. Although aeration did not result in greater organic matter removal efficiencies, it is important to consider the benefits of aeration on the removal of the other compounds. Copyright © 2013 Elsevier Ltd. All rights reserved.

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.

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

Impact of organic-mineral matter interactions on thermal reaction pathways for coal model compounds

Energy Technology Data Exchange (ETDEWEB)

Buchanan, A.C. III; Britt, P.F.; Struss, J.A. [Oak Ridge National Lab., TN (United States). Chemical and Analytical Sciences Div.

1995-07-01

Coal is a complex, heterogeneous solid that includes interdispersed mineral matter. However, knowledge of organic-mineral matter interactions is embryonic, and the impact of these interactions on coal pyrolysis and liquefaction is incomplete. Clay minerals, for example, are known to be effective catalysts for organic reactions. Furthermore, clays such as montmorillonite have been proposed to be key catalysts in the thermal alteration of lignin into vitrinite during the coalification process. Recent studies by Hatcher and coworkers on the evolution of coalified woods using microscopy and NMR have led them to propose selective, acid-catalyzed, solid state reaction chemistry to account for retained structural integrity in the wood. However, the chemical feasibility of such reactions in relevant solids is difficult to demonstrate. The authors have begun a model compound study to gain a better molecular level understanding of the effects in the solid state of organic-mineral matter interactions relevant to both coal formation and processing. To satisfy the need for model compounds that remain nonvolatile solids at temperatures ranging to 450 C, model compounds are employed that are chemically bound to the surface of a fumed silica (Si-O-C{sub aryl}linkage). The organic structures currently under investigation are phenethyl phenyl ether (C{sub 6}H{sub 5}CH{sub 2}CH{sub 2}OC{sub 6}H{sub 5}) derivatives, which serve as models for {beta}-alkyl aryl ether units that are present in lignin and lignitic coals. The solid-state chemistry of these materials at 200--450 C in the presence of interdispersed acid catalysts such as small particle size silica-aluminas and montmorillonite clay will be reported. Initial focus will be on defining the potential impact of these interactions on coal pyrolysis and liquefaction.

Chemical characteristics of dissolved organic matter (DOM) in relation to heavy metal concentrations in soil water from boreal peatlands after clear-cut harvesting

Science.gov (United States)

Kiikkilä, O.; Nieminen, T.; Starr, M.; Ukonmaanaho, L.

2012-04-01

Boreal peatlands form an important terrestrial carbon reserve and are a major source of dissolved organic matter (DOM) to surface waters, particularly when disturbed through forestry practices such as draining or timber harvesting. Heavy metals show a strong affinity to organic matter and so, along with DOM, heavy metals can be mobilized and transported from the soil to surface waters and sediments where they may become toxic to aquatic organisms and pass up the food chain. The complexation of heavy metals with DOM can be expected to be related and determined by the chemical characteristics of DOM and oxidation/reducing conditions in the peat. We extracted interstitial water from peat samples and determined the concentrations of dissolved organic carbon (DOC), dissolved organic nitrogen (DON) and Al, Cu, Zn and Fe in various fractions of DOM isolated by adsorption properties (XAD-8 fractionation) and molecular-weight (ultrafiltration). The peat samples were taken from 0-30 and 30-50 cm depth in drained peatland catchments two years after whole-tree or stem-only clear-cut harvesting (Scots pine or Norway spruce) had been carried out. The samples from the upper layer had been subject to alternating saturation/aeration conditions while the deeper layer had been continuously under the water table. The fractionation of DOC and DON according to both adsorption properties and molecular-weight fractions clearly differed between the upper and lower peat layers. While the hydrophobic acid fraction contained proportionally more DOC and DON than the hydrophilic acid fraction in the upper peat layer the results were vice versa in the lower peat layer. High-molecular-weight compounds (> 100 kDa) were proportionally more abundant in the upper and low-molecular-weight compounds (< 1 kDa) in the lower peat layer. These differences are assumed to reflect differences in the aerobic/ anaerobic conditions and degree of decomposition between the two layers. The concentrations of Zn, Al

Effects of Organic Matter and Clay Content in Soil on Pesticide Adsorption Processes

Directory of Open Access Journals (Sweden)

Rada Đurović

2009-01-01

Full Text Available The effect of organic matter and clay content on the adsorption of atrazine, acetochlor, clomazone, pendimethalin and oxyfluorfen in soil samples was studied. In order to determine whether and to what degree different soil properties affect the process of determinationof selected pesticides, three soils with different clay and organic matter contents were used. An optimized liquid-solid extraction procedure followed by SPME measurement was applied to analyse the selected pesticides in soil samples. Detection and quantificationwere done by gas chromatography-mass spectrometry (GC/MS. Relative standard deviation (RSD values for multiple analyses of soil samples fortified at 30 μg/kg of each pesticide were below 19%. Limits of detection (LODs for all compounds studied were less than 2 μg/kg. The results indicate that soils with different physico-chemical properties have different effects on the adsorption of most pesticides, especially at higher concentration levels.

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

African Journals Online (AJOL)

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

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

Differential chemical fractionation of dissolved organic matter during sorption by Fe mineral phases in a tropical soil from the Luquillo Critical Zone Observatory

Science.gov (United States)

Plante, A. F.; Coward, E.; Ohno, T.; Thompson, A.

2017-12-01

Fe-bearing mineral phases contribute substantially to adsorption and stabilization of soil organic matter (SOM), due largely to their high specific surface area (SSA) and reactivity. While the importance of adsorption onto mineral surfaces has been well-elucidated, selectivity of various mineral and organic phases remains poorly understood. The goals of this work were to: 1) quantify the contributions of Fe-minerals of varying crystallinity to dissolved organic matter (DOM) sorption, and 2) characterize the molecular fractionation of DOM induced by reactions at the mineral interface, using a highly-weathered Oxisol from the Luquillo Critical Zone Observatory (LCZO). Three selective dissolution experiments targeting Fe-mineral phases were followed by specific surface area (SSA) analysis of the residues and characterization of extracted DOM by high resolution mass spectrometry (FT-ICR-MS). Fe-depleted extraction residue samples, untreated control soil samples, and Fe-enriched ferrihydrite-coated soil samples were then subjected to a batch sorption experiment with litter-derived DOM. Results of selective dissolution experiments indicated that a substantial proportion of soil SSA was derived from extracted Fe-bearing phases, and FT-ICR-MS analysis of extracted DOM revealed distinct chemical signatures. Sorbed C concentrations were well correlated with Fe contents induced by treatments, and thus SSA. Molecular characterization of the DOM post-sorption indicated that poorly crystalline Fe phases preferentially adsorbed highly unsaturated aromatic compounds, and higher-crystallinity Fe phases were associated with more aliphatic compounds. These findings suggests that molecular fractionation via organomineral complexation may act as a physicochemical filter of DOM released to the critical zone.

Using organic matter to increase soil fertility in Burundi: potentials and limitations

Science.gov (United States)

Kaboneka, Salvator

2015-04-01

Agriculture production in Burundi is dominated by small scale farmers (0.5 ha/household) who have only very limited access to mineral inputs. In the past, farmers have relied on fallow practices combined with farm yard manures to maintain and improve soil fertility. However, due to the high population growth and high population density (370/km²), fallow practices are nowadays no longer feasible, animal manures cannot be produced in sufficient quantities to maintain soil productivity and food insecurity has become a quasi permanent reality. Most Burundian soils are characterized by 1:1 types of clay minerals (kaolinite) and are acidic in nature. Such soils are of very low cation exchange capacity (CEC). To compare the effect of % clays and % organic matter (% C), correlations tests have been conducted between the two parameters and the CEC. It was found that in high altitude kaolinitic and acidic soils, CEC was highly correlated to % C and less correlated to % clay, suggesting that organic matter could play an important role in improving fertility and productivity of these soils. Based on these findings, additional studies have been conducted to evaluate the fertilizer and soil amendment values of animal manures (cattle, goat, chicken), and leguminous (Calliandra calothyrsus, Gliricidia sepium, Senna simea, Senna spectabilis) and non-leguminous (Tithonia diversifolia) foliar biomass. It was observed that chicken manure significantly reduces Al3+ levels in acidic soils, while Tithonia diversifolia outperforms in nutrient releases compared to the commonly known leguminous agroforestry shrubs and trees indicated above. Although the above mentioned organic sources can contribute to the soil nutrients supply, the quantities potentially available on farm are generally small. The only solution is to supplement these organic sources with other organic sources (compost, organic household waste), chemical fertilizers and mineral amendments (lime) to achieve Integrated Soil

Direct sampling of sub-µm atmospheric particulate organic matter in sub-ng m-3 mass concentrations by proton-transfer-reaction mass spectrometry

Science.gov (United States)

Armin, W.; Mueller, M.; Klinger, A.; Striednig, M.

2017-12-01

A quantitative characterization of the organic fraction of atmospheric particulate matter is still challenging. Herein we present the novel modular "Chemical Analysis of Aerosol Online" (CHARON) particle inlet system coupled to a new-generation proton-transfer-reaction time-of-flight mass spectrometer (PTR-TOF 6000 X2, Ionicon Analytik, Austria) that quantitatively detects organic analytes in real-time and sub-pptV levels by chemical ionization with hydronium reagent ions. CHARON consists of a gas-phase denuder for stripping off gas-phase analytes (efficiency > 99.999%), an aerodynamic lens for particle collimation combined with an inertial sampler for the particle-enriched flow and a thermodesorption unit for particle volatilization prior to chemical analysis. With typical particle enrichment factors of around 30 for particle diameters (DP) between 120 nm and 1000 nm (somewhat reduced enrichment for 60 nm 6000) and excellent mass accuracies (< 10 ppm) chemical compositions can be assigned and included in further analyses. In addition to a detailed characterization of the CHARON PTR-TOF 6000 X2 we will present first results on the chemical composition of sub-µm particulate organic matter in the urban atmosphere in Innsbruck (Austria).

A Prototype Sensor for In Situ Sensing of Fine Particulate Matter and Volatile Organic Compounds.

Science.gov (United States)

Ng, Chee-Loon; Kai, Fuu-Ming; Tee, Ming-Hui; Tan, Nicholas; Hemond, Harold F

2018-01-18

Air pollution exposure causes seven million deaths per year, according to the World Health Organization. Possessing knowledge of air quality and sources of air pollution is crucial for managing air pollution and providing early warning so that a swift counteractive response can be carried out. An optical prototype sensor (AtmOptic) capable of scattering and absorbance measurements has been developed to target in situ sensing of fine particulate matter (PM2.5) and volatile organic compounds (VOCs). For particulate matter testing, a test chamber was constructed and the emission of PM2.5 from incense burning inside the chamber was measured using the AtmOptic. The weight of PM2.5 particles was collected and measured with a filter to determine their concentration and the sensor signal-to-concentration correlation. The results of the AtmOptic were also compared and found to trend well with the Dylos DC 1100 Pro air quality monitor. The absorbance spectrum of VOCs emitted from various laboratory chemicals and household products as well as a two chemical mixtures were recorded. The quantification was demonstrated, using toluene as an example, by calibrating the AtmOptic with compressed gas standards containing VOCs at different concentrations. The results demonstrated the sensor capabilities in measuring PM2.5 and volatile organic compounds.

Cover plants and mineral nitrogen: effects on organic matter fractions in an oxisol under no-tillage in the cerrado

Directory of Open Access Journals (Sweden)

Isis Lima dos Santos

2014-12-01

Full Text Available Cover plants are essential for the sustainability of no-tillage systems in tropical regions. However, information on the effects of these plants and N fertilization on soil organic matter fractions is still scarce. This study evaluated the effect of cover crops with different chemical composition and of N topdressing on the labile and humified organic matter fractions of an Oxisol of the Cerrado (savanna-like vegetation. The study in a randomized complete block design was arranged in split-plots with three replications. Four cover species were tested in the plots and the presence or absence of N topdressing in the subplot. The following cover species were planted in succession to corn for eight years: Urochloa ruziziensis; Canavalia brasiliensis M. ex Benth; Cajanus cajan (L. Millsp; and Sorghum bicolor (L. Moench. In general, the cultivation of U. ruziziensis increased soil C levels, particularly of C in the humic acid and particulate organic C fractions, which are quality indicators of soil organic matter. The C in humic substances and mineral organic C accounted for the highest proportions of total organic C, demonstrating the strong interaction between organic matter, Fe and Al oxides and kaolinite, which are predominant in these weathered soils of the Cerrado.

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.

Organic matter dynamics and N mineralization in grassland soils

NARCIS (Netherlands)

Hassink, J.

1995-01-01

The aims of this study are i) to improve our understanding of the interactions between soil texturelsoil structure, soil organic matter, soil biota and mineralization in grassland soils, ii) to develop a procedure that yields soil organic matter fractions that can be determined directly

Little effects on soil organic matter chemistry of density fractions after seven years of forest soil warming.

Science.gov (United States)

Schnecker, Jörg; Borken, Werner; Schindlbacher, Andreas; Wanek, Wolfgang

2016-12-01

Rising temperatures enhance microbial decomposition of soil organic matter (SOM) and thereby increase the soil CO 2 efflux. Elevated decomposition rates might differently affect distinct SOM pools, depending on their stability and accessibility. Soil fractions derived from density fractionation have been suggested to represent SOM pools with different turnover times and stability against microbial decomposition. To investigate the effect of soil warming on functionally different soil organic matter pools, we here investigated the chemical and isotopic composition of bulk soil and three density fractions (free particulate organic matter, fPOM; occluded particulate organic matter, oPOM; and mineral associated organic matter, MaOM) of a C-rich soil from a long-term warming experiment in a spruce forest in the Austrian Alps. At the time of sampling, the soil in this experiment had been warmed during the snow-free period for seven consecutive years. During that time no thermal adaptation of the microbial community could be identified and CO 2 release from the soil continued to be elevated by the warming treatment. Our results, which included organic carbon content, total nitrogen content, δ 13 C, Δ 14 C, δ 15 N and the chemical composition, identified by pyrolysis-GC/MS, showed no significant differences in bulk soil between warming treatment and control. Surprisingly, the differences in the three density fractions were mostly small and the direction of warming induced change was variable with fraction and soil depth. Warming led to reduced N content in topsoil oPOM and subsoil fPOM and to reduced relative abundance of N-bearing compounds in subsoil MaOM. Further, warming increased the δ 13 C of MaOM at both sampling depths, reduced the relative abundance of carbohydrates while it increased the relative abundance of lignins in subsoil oPOM. As the size of the functionally different SOM pools did not significantly change, we assume that the few and small

Organic matter composition of soil macropore surfaces under different agricultural management practices

Science.gov (United States)

Glæsner, Nadia; Leue, Marin; Magid, Jacob; Gerke, Horst H.

2016-04-01

Understanding the heterogeneous nature of soil, i.e. properties and processes occurring specifically at local scales is essential for best managing our soil resources for agricultural production. Examination of intact soil structures in order to obtain an increased understanding of how soil systems operate from small to large scale represents a large gap within soil science research. Dissolved chemicals, nutrients and particles are transported through the disturbed plow layer of agricultural soil, where after flow through the lower soil layers occur by preferential flow via macropores. Rapid movement of water through macropores limit the contact between the preferentially moving water and the surrounding soil matrix, therefore contact and exchange of solutes in the water is largely restricted to the surface area of the macropores. Organomineral complex coated surfaces control sorption and exchange properties of solutes, as well as availability of essential nutrients to plant roots and to the preferentially flowing water. DRIFT (Diffuse Reflectance infrared Fourier Transform) Mapping has been developed to examine composition of organic matter coated macropores. In this study macropore surfaces structures will be determined for organic matter composition using DRIFT from a long-term field experiment on waste application to agricultural soil (CRUCIAL, close to Copenhagen, Denmark). Parcels with 5 treatments; accelerated household waste, accelerated sewage sludge, accelerated cattle manure, NPK and unfertilized, will be examined in order to study whether agricultural management have an impact on the organic matter composition of intact structures.

Study of the occurrence of organic matter, metals and chemicals in the SFR

International Nuclear Information System (INIS)

Sundqvist, J.O.

2001-03-01

Low- and intermediate level operational waste from the Swedish nuclear power plants, and the Studsvik facility, is currently placed in a repository, termed SFR-l (final repository for radioactive operational waste) near the Forsmark power plant. Two important components in the waste, which can affect the function of the repository, are organic materials, e.g. cloth and paper, and metals (scrap). The release of radionuclides from the repository may be affected by chemical reactions that involve both organic materials and metals. After sealing the repository, the conditions can be such that complexing agents (e.g. isosaccarinic acid) may form when organic materials degrade. These agents typically increase the mobility of radionuclides. Formation of gas, mainly due to metal corrosion, may affect the barrier system, surrounding the waste, such that the release of radionuclides is enhanced. SKB makes an annual report with a compilation of the waste that has been placed in SFR-l . The compilation contains both the amount of waste placed in the repository during the last year and a compilation of the waste that have been placed since the stall of SFR. Moreover, SKB provides a prognosis of the future situation in SFR-1 every third year. SKI (the Swedish Nuclear Power Inspectorate), is responsible for reviewing this reporting. This study was initiated with the purpose of evaluating the uncertainties in SKB's estimates of the amounts of organic matter, metals and chemicals in the waste in SFR- I. The estimates of the quantities of e.g. cellulose and metals in the waste are based on a method which is utilising what is called normal-containers. The waste is classified into certain waste categories. For each waste category there is a specified, presumed composition, named normal-container. The results of this study suggest that the documentation provided by SKB is lacking in some respects. There are for instance examples of incomplete notification of waste and container types

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; Sharma, Saroj K.; Abel, Chol D T; Magic-Knezev, Aleksandra; Song, Kyungguen; Amy, Gary L.

2012-01-01

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

Missing links in the root-soil organic matter continuum

Energy Technology Data Exchange (ETDEWEB)

O' Brien, Sarah L. [Argonne National Laboratory (ANL); Iversen, Colleen M [ORNL

2009-01-01

The soil environment remains one of the most complex and poorly understood research frontiers in ecology. Soil organic matter (SOM), which spans a continuum from fresh detritus to highly processed, mineral-associated organic matter, is the foundation of sustainable terrestrial ecosystems. Heterogeneous SOM pools are fueled by inputs from living and dead plants, driven by the activity of micro- and mesofauna, and are shaped by a multitude of abiotic factors. The specialization required to measure unseen processes that occur on a wide range of spatial and temporal scales has led to the partitioning of soil ecology research across several disciplines. In the organized oral session 'Missing links in the root-soil organic matter continuum' at the annual Ecological Society of America meeting in Albuquerque, NM, USA, we joined the call for greater communication and collaboration among ecologists who work at the root-soil interface (e.g. Coleman, 2008). Our goal was to bridge the gap between scientific disciplines and to synthesize disconnected pieces of knowledge from root-centric and soil-centric studies into an integrated understanding of belowground ecosystem processes. We focused this report around three compelling themes that arose from the session: (1) the influence of the rhizosphere on SOM cycling, (2) the role of soil heterotrophs in driving the transformation of root detritus to SOM, and (3) the controlling influence of the soil environment on SOM dynamics. We conclude with a discussion of new approaches for gathering data to bridge gaps in the root-SOM continuum and to inform the next generation of ecosystem models. Although leaf litter has often been considered to be the main source of organic inputs to soil, Ann Russell synthesized a convincing body of work demonstrating that roots, rather than surface residues, control the accumulation of SOM in a variety of ecosystems. Living roots, which are chemically diverse and highly dynamic, also influence a

Lowering temperature to increase chemical oxidation efficiency: the effect of temperature on permanganate oxidation rates of five types of well defined organic matter, two natural soils, and three pure phase products.

Science.gov (United States)

de Weert, J P A; Keijzer, T J S; van Gaans, P F M

2014-12-01

In situ chemical oxidation (ISCO) is a soil remediation technique to remove organic pollutants from soil and groundwater with oxidants, like KMnO4. However, also natural organic compounds in soils are being oxidized, which makes the technique less efficient. Laboratory experiments were performed to investigate the influence of temperature on this efficiency, through its effect on the relative oxidation rates - by permanganate - of natural organic compounds and organic pollutants at 16 and 15°C. Specific types of organic matter used were cellulose, oak wood, anthracite, reed - and forest peat, in addition to two natural soils. Dense Non-Aqueous Phase Liquid-tetrachloroethene (DNAPL-PCE), DNAPL trichloroethene (DNAPL-TCE) and a mixture of DNAPL-PCE, -TCE and -hexachlorobutadiene were tested as pollutants. Compared to 16°C, oxidation was slower at 5°C for the specific types of organic matter and the natural soils, with exception of anthracite, which was unreactive. The oxidation rate of DNAPL TCE was lower at 5°C too. However, at this temperature oxidation was fast, implying that no competitive loss to natural organic compounds will be expected in field applications by lowering temperature. Oxidation of DNAPL-PCE and PCE in the mixture proceeded at equal rates at both temperatures, due to the dissolution rate as limiting factor. These results show that applying permanganate ISCO to DNAPL contamination at lower temperatures will limit the oxidation of natural organic matter, without substantially affecting the oxidation rate of the contaminant. This will make such remediation more effective and sustainable in view of protecting natural soil quality. Copyright © 2014 Elsevier Ltd. All rights reserved.

From Solute, Fluidic and Particulate Precursors to Complex Organizations of Matter.

Science.gov (United States)

Rao, Ashit; Cölfen, Helmut

2018-03-24

The organization of matter from its constitutive units recruits intermediate states with distinctive degrees of self-association and molecular order. Existing as clusters, droplets, gels as well as amorphous and crystalline nanoparticles, these precursor forms have fundamental contributions towards the composition and structure of inorganic and organic architectures. In this personal account, we show that the transitions from atoms, molecules or ionic species to superstructures of higher order are intertwined with the interfaces and interactions of precursor and intermediate states. Structural organizations distributed across different length scales are explained by the multistep nature of nucleation and crystallization, which can be guided towards functional hybrid materials by the strategic application of additives, templates and reaction environments. Thus, the non-classical pathways for material formation and growth offer conceptual frameworks for elucidating, inducing and directing fascinating material organizations of biogenic and synthetic origins. © 2018 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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.

Complexation of lead by organic matter in Luanda Bay, Angola.

Science.gov (United States)

Leitão, Anabela; Santos, Ana Maria; Boaventura, Rui A R

2015-10-01

Speciation is defined as the distribution of an element among different chemical species. Although the relation between speciation and bioavailability is complex, the metal present as free hydrated ion, or as weak complexes able to dissociate, is usually more bioavailable than the metal incorporated in strong complexes or adsorbed on colloidal or particulate matter. Among the analytical techniques currently available, anodic stripping voltammetry (ASV) has been one of the most used in the identification and quantification of several heavy metal species in aquatic systems. This work concerns the speciation study of lead, in original (natural, non-filtered) and filtered water samples and in suspensions of particulate matter and sediments from Luanda Bay (Angola). Complexes of lead with organics were identified and quantified by differential pulse anodic stripping voltammetry technique. Each sample was progressively titrated with a Pb(II) standard solution until complete saturation of the organic ligands. After each addition of Pb(II), the intensity, potential and peak width of the voltammetric signal were measured. The results obtained in this work show that more than 95 % of the lead in the aquatic environment is bound in inert organic complexes, considering all samples from different sampling sites. In sediment samples, the lead is totally (100 %) complexed with ligands adsorbed on the particles surface. Two kinds of dominant lead complexes, very strong (logK >11) and strong to moderately strong (8< logK <11), were found, revealing the lead affinity for the stronger ligands.

Radionuclide - Soil Organic Matter Interactions

DEFF Research Database (Denmark)

Carlsen, Lars

1985-01-01

Interactions between soil organic matter, i.e. humic and fulvic acids, and radionuclides of primary interest to shallow land burial of low activity solid waste have been reviewed and to some extent studied experimentally. The radionuclides considered in the present study comprise cesium, strontium...

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

Science.gov (United States)

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

2013-02-01

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

Quantities and qualities of physical and chemical fractions of soil organic matter under a rye cover crop

Science.gov (United States)

To detect the effects of a rye cover crop on labile soil carbon, the light fraction, large particulate organic matter (POM), small POM, and two NaOH-extractable humic fractions were extracted from three depths of a corn soil in central Iowa having an overwinter rye cover crop treatment and a contro...

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.

[Evolution of Dissolved Organic Matter Properties in a Constructed Wetland of Xiao River, Hebei].

Science.gov (United States)

Ma, Li-na; Zhang, Hui; Tan, Wen-bing; Yu, Min-da; Huang, Zhi-gang; Gao, Ru-tai; Xi, Bei-dou; He, Xiao-song

2016-01-01

The evolution of water DOC and COD, and the source, chemical structure, humification degree and redox of dissolved organic matter (DOM) in a constructed wetland of Xiao River, Hebei, was investigated by 3D excitation--emission matrix fluorescence spectroscopy coupled with ultraviolet spectroscopy and chemical reduction, in order to explore the geochemical processes and environmental effects of DOM. Although DOC contributes at least 60% to COD, its decrease in the constructed wetland is mainly caused by the more extensive degradation of elements N, H, S, and P than C in DOM, and 65% is contributed from the former. DOM is mainly consisted of microbial products based on proxies f470/520 and BIX, indicating that DOM in water is apparently affected by microbial degradation. The result based on PARAFAC model shows that DOM in the constructed wetland contains protein-like and humus-like components, and Fulvic- and humic-like components are relatively easier to degrade than protein-like components. Fulvic- and humic-like components undergo similar decomposition in the constructed wetland. A common source of chromophoric dissolved organic matter (CDOM) and fluorescent dissolved organic matter (FDOM) exists; both CDOM and FDOM are mainly composed of a humus-like material and do not exhibit selective degradation in the constructed wetland. The proxies E2 /E3, A240-400, r(A, C) and HIX in water have no changes after flowing into the constructed wetland, implying that the humification degree of DOM in water is hardly affected by wet constructed wetland. However, the constructed wetland environment is not only beneficial in forming the reduced state of DOM, but also facilitates the reduction of ferric. It can also improve the capability of DOM to function as an electron shuttle. This result may be related to the condition that the aromatic carbon of DOM can be stabilized well in the constructed wetland.

Liming effects on the chemical composition of the organic surface layer of a mature Norway spruce stand (Picea abies [L.] Karst.)

NARCIS (Netherlands)

Rosenberg, W.; Nierop, K.G.J.; Knicker, H.; Jager, de P.A.; Kreutzer, K.; Weiá, T.

2003-01-01

The application of lime in a mature Norway spruce (Picea abies [L.] Karst.) forest in southern Germany induced major changes in the activity of soil organisms and root growth. Since this may influence the chemical compostion of the soil organic matter (SOM) of the organic surface layer, its

Mobility of the dissolved organic matter through intact boom clay cores

International Nuclear Information System (INIS)

Put, M.J.; Dierckx, A.; Aertsens, M.; Canniere, P. de

1998-01-01

Performance assessment studies are expected to predict the enhancement of the migration of trivalent lanthanides and actinides due to their complexation with organic matter, which play a role as a transport agent [1]. Therefore, the mobility of the dissolved organic matter in the interstitial boom clay water is studied. For the first time, the mobile fraction present in the clay water is concentrated and labelled with a radioisotope to study the mobility of the organic matter in clay and the interaction of the mobile with the non-mobile. The isotopes tested as label are 125 I and 14 C. The 125 I label proved to be unstable and hence discarded. The labelled organic matter is then diluted for migration experiments on boom clay cores under anaerobic conditions. The influence of the molecular size on its mobility is studied by the separation of the labelled organic matter in different size fractions. (orig.)

Organic matter in uranium concentration during ancient bed oxidation of carboniferons sediments

International Nuclear Information System (INIS)

Kruglova, V.G.; Uspenskij, V.A.; Dement'ev, P.K.; Kochenov, A.V.

1984-01-01

Changes in the organic matter accompanying the process of epigenetic ore formation are studied using the example of a deposit localized in carboniferous molasse strata of the Cretaceous period. Peculiarities of the organic matter as the main mineralization agent are studied by a complex of physical and themical methods. A distinct relationship between the uranium concentration and the degree of organic matter oxigenation is a most characteristic feature of the ore localization, however, there is no direct correlation between the contents of uranium and organic matter in ores. Uranium minerallzation was accumulated during infiltration of acid uraniferous.waters into grey stratum in the process of the bed oxidation zone formation oxidizing. Brown coal matter possessing a maximum adsorbability, as compared to other sedimentary rocks, apprared to be the uranium precipitator. The adsorption was accompanie by the formation of proper uranium minerals (coffinite, pitchblende) due to uranium reduction by oxidizing organic matter. Thus, the oxidative epigenesis was an are-forming process with the uranium concentration on organic matter proportionally to oxidation of the latter

A Prototype Sensor for In Situ Sensing of Fine Particulate Matter and Volatile Organic Compounds

Directory of Open Access Journals (Sweden)

Chee-Loon Ng

2018-01-01

Full Text Available Air pollution exposure causes seven million deaths per year, according to the World Health Organization. Possessing knowledge of air quality and sources of air pollution is crucial for managing air pollution and providing early warning so that a swift counteractive response can be carried out. An optical prototype sensor (AtmOptic capable of scattering and absorbance measurements has been developed to target in situ sensing of fine particulate matter (PM2.5 and volatile organic compounds (VOCs. For particulate matter testing, a test chamber was constructed and the emission of PM2.5 from incense burning inside the chamber was measured using the AtmOptic. The weight of PM2.5 particles was collected and measured with a filter to determine their concentration and the sensor signal-to-concentration correlation. The results of the AtmOptic were also compared and found to trend well with the Dylos DC 1100 Pro air quality monitor. The absorbance spectrum of VOCs emitted from various laboratory chemicals and household products as well as a two chemical mixtures were recorded. The quantification was demonstrated, using toluene as an example, by calibrating the AtmOptic with compressed gas standards containing VOCs at different concentrations. The results demonstrated the sensor capabilities in measuring PM2.5 and volatile organic compounds.

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...

Effect of food processing organic matter on photocatalytic bactericidal activity of titanium dioxide (TiO2).

Science.gov (United States)

Yemmireddy, Veerachandra K; Hung, Yen-Con

2015-07-02

The purpose of this study was to determine the effect of food processing organic matter on photocatalytic bactericidal activity of titanium dioxide (TiO2) nanoparticles (NPs). Produce and meat processing wash solutions were prepared using romaine lettuce and ground beef samples. Physico-chemical properties such as pH, turbidity, chemical oxygen demand (COD), total phenolics (for produce) and protein (for meat) content of the extracts were determined using standard procedures. The photocatalytic bactericidal activity of TiO2 (1 mg/mL) in suspension with or without organic matter against Escherichia coli O157:H7 (5-strain) was determined over a period of 3h. Increasing the concentration of organic matter (either produce or meat) from 0% to 100% resulted in 85% decrease in TiO2 microbicidal efficacy. 'Turbidity, total phenolics, and protein contents in wash solutions had significant effect on the log reduction. Increasing the total phenolics content in produce washes from 20 to 114 mg/L decreased the log reduction from 2.7 to 0.38 CFU/mL, whereas increasing the protein content in meat washes from 0.12 to 1.61 mg/L decreased the log reduction from and 5.74 to 0.87 CFU/mL. Also, a linear correlation was observed between COD and total phenolics as well as COD and protein contents. While classical disinfection kinetic models failed to predict, an empirical equation in the form of "Y=me(nX)" (where Y is log reduction, X is COD, and m and n are reaction rate constants) predicted the disinfection kinetics of TiO2 in the presence of organic matter (R(2)=94.4). This study successfully identified an empirical model with COD as a predictor variable to predict the bactericidal efficacy of TiO2 when used in food processing environment. Copyright © 2015 Elsevier B.V. All rights reserved.

Transuranium elements in organic chemical forms

International Nuclear Information System (INIS)

Sakanoue, Masanobu; Yamamoto, Masayoshi

1987-01-01

It is very important to achive an understanding what role organic matter plays in the behavior of transuranium elements in the environment. This paper reports the studies on characteristics of fallout Pu and Am in soil closely related to soil organic matter, and interaction of humic acid and Am (III) in aqueous solution. From the results obtained, it was suggested that the humic acids had strong interaction with transuranium elements, but such soluble complexes were removed soon from the solution by coagulation and sorption on soil. (author)

Chemical imaging techniques for the analysis of complex mixtures: New application to the characterization of ritual matters on African wooden statuettes

International Nuclear Information System (INIS)

Mazel, Vincent; Richardin, Pascale; Touboul, David; Brunelle, Alain; Walter, Philippe; Laprevote, Olivier

2006-01-01

Chemical imaging techniques, based on the combination of microscopy and spectroscopy, are well suited to study both the composition and the spatial organization of heterogeneous complex mixtures of organic and mineral matter. Time-of-flight secondary ion mass spectrometry (ToF-SIMS), followed by scanning electron microscopy with energy dispersive X-ray analysis (SEM-EDX) and Fourier transform infrared microscopy (FTIR microscopy) have been applied to non-destructive analysis of micro-samplings of ritual matters deposited on the surface of African wooden statuettes. With a very careful preparation, using ultramicrotomy on embedded samples, it was possible to perform successively all the measurements on a single fragment. Comparison and superposition of the different chemical images, obtained on a sample from a significant actual artefact, have allowed us to identify minerals (clays, quartz and calcium carbonate), proteins, starch, urate salts and lipids and to map their spatial distribution

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

Chemical, green and organic manure effects on chemical properties on a savannah oxisol and on corn under conventional tillage and no-tillage

Science.gov (United States)

Mannigel, Anny R.; Alves, Marlene C.; Valério Filho, Walter V.

2015-04-01

Modern agriculture, in general, has always been based on the concept that natural resources are endless; however, this concept is changing. Concern for the environment is increasingly becoming part of farming practices, either by the awareness of society, or because the high cost of fertilizers or even the exhaustion of soils. The objective of this research was to evaluate the effects of the green manure and mineral fertilizer and/or organic manure and, on the chemical properties of an Oxisol, on "Savannah" (cerrado) area in Mato Grosso do Sul-Brazil, cultivated with corn (Zea mays L.) on the following management conditions: no-tillage and conventional tillage, on area previously under pasture (Brachiaria decumbens). The experimental design was a randomized blocks and the tested treatments were: control (without organic manure or chemical fertilizer); chemical fertilizer, as recommended for the culture and based on the chemical soil analysis; organic manure (cow manure); organic manure + half of the mineral fertilizer recommended rate; and the green manure Crotalaria juncea and Pennisetum americanum. The chemical analyses were the soil chemical analysis to the intent of soil fertility. Corn yield was evaluated. The collect of soil samples were realized in depths of 0.00-0.05 m and 0.05-0.10 m and 0.10-0.20 m. The organic manure and the organic manure + half of the mineral recommended rate increased P, Ca, Mg, K and Organic Matter in the first depth (0.00 - 0.05 m). These treatments also increased K and Mg at the second depth analyzed (0.05 - 0.10 m) and K in the depth from 0.10 - 0.20 m. Under conventional tillage management presents better crop results with an average grain yield of 3649 kg ha-1 versus 2374 kg ha-1 obtained under no-tillage. The use of chemical fertilizer, organic manure + half of the mineral recommended rate, Crotalaria juncea, organic manure and Pennisetum americanum increased corn yield by 84, 79, 58, 44 and 41 %, respectively.

ES1406 COST Action: Soil fauna: Key to Soil Organic Matter Dynamicsand Fertility. How far have we got?

DEFF Research Database (Denmark)

Jiménez, Juan; Filser, Juliane; Barot, Sébastien

Soil organic matter (SOM) is key to soil fertility, climate change mitigation, combatting land degradation, and the conservation of above- and below-ground biodiversity and associated ecosystem services like decomposition, nutrient cycling, carbon sequestration, detoxification and maintenance...... of soil physico-chemical properties. SOM dynamics represent the balance between the input of plant material (residues, root-derived materials) and the output through decomposition (OM mineralization) by organisms, erosion and leaching. Approximately 20% of global CO2 emissions, one third of global CH4...... emissions and two thirds of N2O emissions originate from soils. In many soils, most of the macro-aggregate structure is formed by the activities of soil invertebrates and roots, with important consequences for soil organic matter dynamics, carbon sequestration and water infiltration at several spatial...

Molecular simulation of a model of dissolved organic matter.

Science.gov (United States)

Sutton, Rebecca; Sposito, Garrison; Diallo, Mamadou S; Schulten, Hans-Rolf

2005-08-01

A series of atomistic simulations was performed to assess the ability of the Schulten dissolved organic matter (DOM) molecule, a well-established model humic molecule, to reproduce the physical and chemical behavior of natural humic substances. The unhydrated DOM molecule had a bulk density value appropriate to humic matter, but its Hildebrand solubility parameter was lower than the range of current experimental estimates. Under hydrated conditions, the DOM molecule went through conformational adjustments that resulted in disruption of intramolecular hydrogen bonds (H-bonds), although few water molecules penetrated the organic interior. The radius of gyration of the hydrated DOM molecule was similar to those measured for aquatic humic substances. To simulate humic materials under aqueous conditions with varying pH levels, carboxyl groups were deprotonated, and hydrated Na+ or Ca2+ were added to balance the resulting negative charge. Because of intrusion of the cation hydrates, the model metal-humic structures were more porous, had greater solvent-accessible surface areas, and formed more H-bonds with water than the protonated, hydrated DOM molecule. Relative to Na+, Ca2+ was both more strongly bound to carboxylate groups and more fully hydrated. This difference was attributed to the higher charge of the divalent cation. The Ca-DOM hydrate, however, featured fewer H-bonds than the Na-DOM hydrate, perhaps because of the reduced orientational freedom of organic moieties and water molecules imposed by Ca2+. The present work is, to our knowledge, the first rigorous computational exploration regarding the behavior of a model humic molecule under a range of physical conditions typical of soil and water systems.

Generation of dissolved organic matter and byproducts from activated sludge during contact with sodium hypochlorite and its implications to on-line chemical cleaning in MBR.

Science.gov (United States)

Cai, Weiwei; Liu, Jiaqi; Zhang, Xiangru; Ng, Wun Jern; Liu, Yu

2016-11-01

On-line chemical cleaning of membranes with sodium hypochlorite (NaClO) has been commonly employed for maintaining a constant permeability of membrane bioreactor (MBR) due to its simple and efficient operation. However, activated sludge is inevitably exposed to NaClO during this cleaning process. In spite of the broad applications of on-line chemical cleaning in MBR such as chemical cleaning-in-place (CIP) and chemical enhanced backwash (CEB), little information is currently available for the release of emerging dissolved organic matter (DOM) and byproducts from this prevalent practice. Therefore, in this study, activated sludge suspended in a phosphate buffered saline solution was exposed to different doses of NaClO in order to determine the generation of potential DOM and byproducts. The results showed the occurrence of significant DOM release (up to 24.7 mg/L as dissolved organic carbon) after exposure to NaClO for 30 min. The dominant components of the released DOM were characterized to be humic acid-like as well as protein-like substances by using an excitation-emission matrix fluorescence spectrophotometer. Furthermore, after the contact of activated sludge with NaClO, 19 kinds of chlorinated and brominated byproducts were identified by ultra performance liquid chromatography/electrospray ionization-triple quadrupole mass spectrometry, eight of which were confirmed and characterized with standard compounds. Many byproducts were found to be halogenated aromatic compounds, including halopyrroles and halo(hydro)benzoquinones, which had been reported to be significantly more toxic than the halogenated aliphatic ones. Consequently, this study offers new insights into the practice of on-line chemical cleaning, and opens up a window to re-examine the current operation of MBR by looking into the generation of micropollutants. Copyright © 2016 Elsevier Ltd. All rights reserved.

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...

Molecular building blocks and their architecture in biologically/environmentally compatible soft matter chemical machinery.

Science.gov (United States)

Toyota, Taro; Banno, Taisuke; Nitta, Sachiko; Takinoue, Masahiro; Nomoto, Tomonori; Natsume, Yuno; Matsumura, Shuichi; Fujinami, Masanori

2014-01-01

This review briefly summarizes recent developments in the construction of biologically/environmentally compatible chemical machinery composed of soft matter. Since environmental and living systems are open systems, chemical machinery must continuously fulfill its functions not only through the influx and generation of molecules but also via the degradation and dissipation of molecules. If the degradation or dissipation of soft matter molecular building blocks and biomaterial molecules/polymers can be achieved, soft matter particles composed of them can be used to realize chemical machinery such as selfpropelled droplets, drug delivery carriers, tissue regeneration scaffolds, protocell models, cell-/tissuemarkers, and molecular computing systems.

Reproducing the organic matter model of anthropogenic dark earth of Amazonia and testing the ecotoxicity of functionalized charcoal compounds

Directory of Open Access Journals (Sweden)

Carolina Rodrigues Linhares

2012-05-01

Full Text Available The objective of this work was to obtain organic compounds similar to the ones found in the organic matter of anthropogenic dark earth of Amazonia (ADE using a chemical functionalization procedure on activated charcoal, as well as to determine their ecotoxicity. Based on the study of the organic matter from ADE, an organic model was proposed and an attempt to reproduce it was described. Activated charcoal was oxidized with the use of sodium hypochlorite at different concentrations. Nuclear magnetic resonance was performed to verify if the spectra of the obtained products were similar to the ones of humic acids from ADE. The similarity between spectra indicated that the obtained products were polycondensed aromatic structures with carboxyl groups: a soil amendment that can contribute to soil fertility and to its sustainable use. An ecotoxicological test with Daphnia similis was performed on the more soluble fraction (fulvic acids of the produced soil amendment. Aryl chloride was formed during the synthesis of the organic compounds from activated charcoal functionalization and partially removed through a purification process. However, it is probable that some aryl chloride remained in the final product, since the ecotoxicological test indicated that the chemical functionalized soil amendment is moderately toxic.

Use of native aquatic macrophytes in the reduction of organic matter from dairy effluents.

Science.gov (United States)

Queiroz, Rita de Cássia Souza de; Andrade, Rodrigo Santos; Dantas, Isadora Rosário; Ribeiro, Vinícius de Souza; Neto, Luciano Brito Rodrigues; Almeida Neto, José Adolfo de

2017-08-03

Considering the diversity and the unexplored potential of regional aquatic flora, this study aimed to identify and analyze the potential of native aquatic macrophytes to reduce the organic matter of dairy wastewater (DW) using experimental constructed wetlands. The dairy wastewater (DW) had an average chemical oxygen demand (COD) of 7414.63 mg/L and then was diluted to 3133.16 mg/L (D1) and to 2506.53 mg/L (D2). Total solids, COD, temperature, and pH analyses were performed, and the biochemical oxygen demand (BOD) was estimated from the COD values. The best performance in the reduction of the organic matter was observed for Polygonum sp. (87.5% COD and 79.6% BOD) and Eichhornia paniculata (90% COD and 83.7% BOD) at dilution D1, on the 8th day of the experiment. However, the highest total solids removal was observed for Polygonum sp. (32.2%), on the 4th day, at dilution D2. The total solid (TS) concentration has also increased starting from the 8th day of the experiment was observed which may have been due to the development of mosquito larvae and their mechanical removal by sieving, thus changing the steady state of the experimental systems. The macrophytes Polygonum sp. and E. paniculata were considered suitable for the reduction of organic matter of DW using constructed wetlands.

Simultaneous removal of organic matter and salt ions from saline wastewater in bioelectrochemical systems

KAUST Repository

Kim, Younggy

2013-01-01

A new bioelectrochemical system is proposed for simultaneous removal of salinity and organic matter. In this process, exoelectrogenic microorganisms oxidize organic matter and transfer electrons to the anode, hydrogen is evolved at the cathode by supplying additional voltage, and salt is removed from the wastewater due to the electric potential generated and the use of two ion-exchange membranes. Salinity removal (initial conductivity ~40mS/cm) increased from 21 to 84% by increasing the substrate (sodium acetate) from 2 to 8g/L. A total of 72-94% of the chemical oxygen demand was degraded in the anode and cathode chambers, with 1-4% left in the anode chamber and the balance lost through the anion-exchange membrane into the concentrate waste chamber. The maximum hydrogen production rate was 3.6m3-H2/m3-electrolyte per day at an applied potential of 1.2V. The Coulombic efficiency was ~100%, while the cathode recovery varied from 57 to 100%, depending on the extent of methanogenesis. Exoelectrogenic microbes generated high current densities (7.8mA/cm2) at ≤36g/L of total dissolved solids, but >41g/L eliminated current. These results provide a new method for achieving simultaneous removal of salinity and organic matter from a saline wastewater with H2 production. © 2012 Elsevier B.V.

Trials and Tribulations of Fluorescent Dissolved Organic Matter Chemical Interpretations: A case study of polar ice cores

Science.gov (United States)

D'Andrilli, J.

2017-12-01

Excitation emission matrix fluorescence spectroscopy is widely applied for rapid dissolved organic matter (DOM) characterization in aquatic systems. Fluorescent DOM surveys are booming, not only as a central focus in aquatic environments, but also as an important addition to interdisciplinary research (e.g., DOM analysis in concert with ice core paleoclimate reconstructions, stream metabolism, hydrologic regimes, agricultural developments, and biological activity), opening new doors, not just for novelty, but also for more challenges with chemical interpretations. Recently, the commonly used protein- versus humic-like classifications of DOM have been ineffective at describing DOM chemistry in various systems (e.g., ice cores, wastewaters, incubations/engineered). Moreover, the oversimplification of such classifications used to describe fluorescing components, without further scrutiny, has become commonplace, ultimately producing vague reporting. For example, West Antarctic ice core DOM was shown to contain fluorescence in the low excitation/emission wavelength region, however resolved fluorophores depicting tyrosine- and tryptophan-like DOM were not observed. At first, as literature suggested, we reported this result as protein-like, and concluded that microbial contributions were dominant in deep ice. That initial interpretation would disintegrate the conservation paradigm of atmospheric composition during deposition, the crux of ice core research, and contradict other lines of evidence. This begged the question, "How can we describe DOM chemistry without distinct fluorophores?" Antarctic ice core DOM was dominated by neither tyrosine- nor tryptophan-like fluorescence, causing "unusual" looking fluorescent components. After further examination, deep ice DOM was reported to contain fluorescent species most similar to monolignols and tannin-like phenols, describing the precursors of lignin from low carbon producing environments, consistent with marine sediment

Spectral band selection for classification of soil organic matter content

Science.gov (United States)

Henderson, Tracey L.; Szilagyi, Andrea; Baumgardner, Marion F.; Chen, Chih-Chien Thomas; Landgrebe, David A.

1989-01-01

This paper describes the spectral-band-selection (SBS) algorithm of Chen and Landgrebe (1987, 1988, and 1989) and uses the algorithm to classify the organic matter content in the earth's surface soil. The effectiveness of the algorithm was evaluated comparing the results of classification of the soil organic matter using SBS bands with those obtained using Landsat MSS bands and TM bands, showing that the algorithm was successful in finding important spectral bands for classification of organic matter content. Using the calculated bands, the probabilities of correct classification for climate-stratified data were found to range from 0.910 to 0.980.

The role of organic matter in the removal of emerging trace organic chemicals during managed aquifer recharge.

Science.gov (United States)

Rauch-Williams, T; Hoppe-Jones, C; Drewes, J E

2010-01-01

This study explored the effect of different bulk organic carbon matrices on the fate of trace organic chemicals (TOrC) during managed aquifer recharge (MAR). Infiltration through porous media was simulated in biologically active column experiments under aerobic and anoxic recharge conditions. Wastewater effluent derived organic carbon types, differing in hydrophobicity and biodegradability (i. e., hydrophobic acids, hydrophilic carbon, organic colloids), were used as feed substrates in the column experiments. These carbon substrates while fed at the same concentration differed in their ability to support soil biomass growth during porous media infiltration. Removal of degradable TOrC (with the exception of diclofenac and propyphenazone) was equal or better under aerobic versus anoxic porous media infiltration conditions. During the initial phase of infiltration, the presence of biodegradable organic carbon (BDOC) enhanced the decay of degradable TOrC by promoting soil biomass growth, suggesting that BDOC served as a co-substrate in a co-metabolic transformation of these contaminants. However, unexpected high removal efficiencies were observed for all degradable TOrC in the presence of low BDOC concentrations under well adopted oligotrophic conditions. It is hypothesized that removal under these conditions is caused by a specialized microbial community growing on refractory carbon substrates such as hydrophobic acids. Findings of this study reveal that the concentration and character of bulk organic carbon present in effluents affect the degradation efficiency for TOrC during recharge operation. Specifically aerobic, oligotrophic microbiological soil environments present favorable conditions for the transformation of TOrC, including rather recalcitrant compounds such as chlorinated flame retardants. (c) 2009 Elsevier Ltd. All rights reserved.

Changes in soil organic matter compositrion after introduction of riparian vegetation on shores of hydroelectric reservoires (Southeast of Brazil)

NARCIS (Netherlands)

Alcantara, de F.A.; Buurman, P.; Curi, N.; Furtini Neto, A.E.; Lagen, van B.; Meijer, E.M.

2004-01-01

This work is part of a research program with the general objective of evaluating soil sustainability in areas surrounding hydroelectric reservoirs, which have been planted with riparian forest. The specific aims were: (i) to assess if and how the soil organic matter (SOM) chemical composition has

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.

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

Advanced characterization of dissolved organic matter released by bloom-forming marine algae

KAUST Repository

Rehman, Zahid Ur

2017-06-01

Algal organic matter (AOM), produced by marine phytoplankton during bloom periods, may adversely affect the performance of membrane processes in seawater desalination. The polysaccharide fraction of AOM has been related to (bio)fouling in micro-filtration and ultrafiltration, and reverse osmosis membranes. However, so far, the chemical structure of the polysaccharides released by bloom-forming algae is not well understood. In this study, dissolved fraction of AOM produced by three algal species (Chaetoceros affinis, Nitzschia epithemoides and Hymenomonas spp.) was characterized using liquid chromatography–organic carbon detection (LC-OCD) and fluorescence spectroscopy. Chemical structure of polysaccharides isolated from the AOM solutions at stationary phase was analyzed using proton nuclear magnetic resonance (H-NMR). The results showed that production and composition of dissolved AOM varied depending on algal species and their growth stage. AOM was mainly composed of biopolymers (BP; i.e., polysaccharides and proteins [PN]), but some refractory substances were also present.H-NMR spectra confirmed the predominance of carbohydrates in all samples. Furthermore, similar fingerprints were observed for polysaccharides of two diatom species, which differed considerably from that of coccolithophores. Based on the findings of this study,H-NMR could be used as a method for analyzing chemical profiles of algal polysaccharides to enhance the understanding of their impact on membrane fouling.

Effect of phosphorus and organic matter on zinc availability on rice

International Nuclear Information System (INIS)

Gupta, G.N.; Kamath, M.B.; Motsara, M.R.

1977-01-01

Pot culture experiment was conducted on grey brown podzolic soil (Palampur) and Tarai soil (Pantnagar) to study the influence of the addition of organic matter, phosphorus and zinc on the uptake and utilization of zinc by rice crop. In podzolic soils the combined application of Zn-P and Zn-organic matter resulted in reduced zinc content in crop but the crop yield was not affected. The uptake and utilization of applied zinc increased with P application. In Tarai soil, crop response to Zn, P and organic matter was obtained when applied separately. A negative zinc x P and zinc x organic matter interaction was obtained on yield. However, zinc content of the crop increased due to the application of P, organic matter and zinc. The uptake and utilization of applied zinc increased with P application. The analysis of soils after crop harvest indicated an increased amount of 0.1 N HCl extractable zinc in soils treated with zinc in Tarai soils while in podzolic soil from Palampur, the available zinc increased only under the combined application of zinc and P. (author)

Response of organic matter quality in permafrost soils to warming

Science.gov (United States)

Plaza, C.; Pegoraro, E.; Schuur, E.

2016-12-01

Global warming is predicted to thaw large quantities of the perennially frozen organic matter stored in northern permafrost soils. Upon thaw, this organic matter will be exposed to lateral export to water bodies and to microbial decomposition, which may exacerbate climate change by releasing significant amounts of greenhouse gases. To gain an insight into these processes, we investigated how the quality of permafrost soil organic matter responded to five years of warming. In particular, we sampled control and experimentally warmed soils in 2009 and 2013 from an experiment established in 2008 in a moist acidic tundra ecosystem in Healy, Alaska. We examined surface organic (0 to 15 cm), deep organic (15 to 35 cm), and mineral soil layers (35 to 55 cm) separately by means of stable isotope analysis (δ13C and δ15N) and solid-state 13C nuclear magnetic resonance. Compared to the control, the experimental warming did not affect the isotopic and molecular composition of soil organic matter across the depth profile. However, we did find significant changes with time. In particular, in the surface organic layer, δ13C decreased and alkyl/O-alkyl ratio increased from 2009 to 2013, which indicated variations in soil organic sources (e.g., changes in vegetation) and accelerated decomposition. In the deep organic layer, we found a slight increase in δ15N with time. In the mineral layer, δ13C values decreased slightly, whereas alkyl C/O-alkyl ratio increased, suggesting a preferential loss of relatively more degraded organic matter fractions probably by lateral transport by water flowing through the soil. Acknowledgements: This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No. 654132. Web site: http://vulcan.comule.com

Effects of compost organic amendments on chemical composition and in vitro digestibility of alfalfa (Medicago sativa L.

Directory of Open Access Journals (Sweden)

Francesco Montemurro

2010-01-01

Full Text Available The following fertiliser treatments were compared during the years 2002 and 2003 on alfalfa forage (Medicago sativa L.: compost obtained from the organic fraction of the Municipal Solid Waste (MSW; olive pomace compost (OPC; mineral fertiliser (Min. All the treatments allowed a distribution of 75kg ha-1 of P2O5. Three cuttings occurred: at 168, 206 and 351 days after compost application (DAA in 2002; 119, 152 and 320 DAA in 2003. Cumulative biomass and dry matter yields were measured during each experimental year. Furthermore, chemical composition and in vitro digestibility of dry matter (DMd, organic matter (OMd, crude protein (CPd and NDF (NDFd were determined. MSW treatment showed a significantly (P<0.01 higher content of ADL than OPC and Min (77.0, 66.0 and 65.0g kg-1 DM, respectively. Fertiliser treatments also affected (P<0.01 digestibility parameters. In fact, DMd and OMd values showed the same trend with lower percentages in MSW treatment than in the OPC and Min ones. The NDFd differed in all treatments having the highest value in OPC (40.1%. The results indicated that the soil distribution of organic materials offer the possibility to reduce the application of mineral fertilisers and production costs without decreasing alfalfa yield, forage chemical composition and in vitro digestibility.

Mid-infrared study of the molecular structure variability of insoluble organic matter from primitive chondrites

Science.gov (United States)

Orthous-Daunay, F.-R.; Quirico, E.; Beck, P.; Brissaud, O.; Dartois, E.; Pino, T.; Schmitt, B.

2013-03-01

Insoluble Organic Matter (IOM) found in primitive meteorites was formed in the Early Solar System and subsequently processed on the parent asteroids. The location, temporal sequence and processes of formation of this IOM are still a matter of debate. In particular, there is no consensus on the actual effect of post-accretional aqueous alteration processes on the chemical composition and structure of IOM. In the most primitive chondrites (types 1 and 2), these alterations have so far been either neglected or generically assigned to oxidation processes induced by fluid circulation. A series of IOM samples extracted from 14 chondrites with extensively documented post-accretional histories have been studied by infrared spectroscopy. Aqueous alteration shows no detectable effect on the chemical composition and structure of IOM within or across chondrite classes. Indeed, the most effective post-accretional process appears to be a high-temperature short-duration heating event and concerns essentially type 2 chondrites. In any case, post-accretional processes cannot account for all the chemical and structural variations of IOM. Chondrites from the CI, CR and CM classes accreted IOM precursors with moderately variable compositions, suggesting a chemical heterogeneity of the protosolar disk. The 3.4 μm band, and possibly its overtones and combinations in the near-infrared range, appear to be tracer(s) of the chemical class and possibly of surface heating processes triggered by impacts.

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.

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

Controlled experimental soil organic matter modification for study of organic pollutant interactions in soil

International Nuclear Information System (INIS)

Ahmed, Ashour A.; Kühn, Oliver; Leinweber, Peter

2012-01-01

Interactions of organic pollutants with soil organic matter can be studied by adsorption of the pollutants on well-characterized soil samples with constant mineralogy but different organic matter compositions. Therefore, the objectives of the current study are establishing a set of different, well-characterized soil samples by systematic modifications of their organic matter content and molecular composition and prove these modifications by advanced complementary analytical techniques. Modifications were done by off-line pyrolysis and removal/addition of hot-water extracted organic fraction (HWE) from/to the original soil sample. Both pyrolysis-field ionization mass spectrometry (Py-FIMS) and synchrotron-based C- and N- X-ray absorption near-edge structure spectroscopy (XANES) were applied to investigate the composition of the soil organic matter. These complementary analytical methods in addition to elemental analysis agreed in showing the following order of organic matter contents: pyrolyzed soil < soil residue < original soil < soil + 3 HWE < soil + 6 HWE < HWE. The addition of HWE to the soil sample increases the relative proportions of carbohydrates, N-containing heterocyclic compounds and peptides, and decreases the relative proportions of phenols, lignin monomers and dimers, and lipids. The most abundant organic compound classes in the pyrolyzed sample are aromatics, aliphatic nitriles, aldehydes, five- and six-membered N-containing heterocyclic compounds, and aliphatic carboxylic acids. It can be expected that removal or addition of HWE, that mimic biomass inputs to soil or soil amendments, change the binding capacity for organic pollutants less intensively than heat impact, e.g. from vegetation burning. It will be possible to interpret kinetic data on the pollutants adsorption by these original and modified soil samples on the basis of the bond- and element-specific speciation data through C-XANES and N-XANES and the molecular-level characterization

Chemical equilibrium modeling of organic acids, pH, aluminum, and iron in Swedish surface waters.

Science.gov (United States)

Sjöstedt, Carin S; Gustafsson, Jon Petter; Köhler, Stephan J

2010-11-15

A consistent chemical equilibrium model that calculates pH from charge balance constraints and aluminum and iron speciation in the presence of natural organic matter is presented. The model requires input data for total aluminum, iron, organic carbon, fluoride, sulfate, and charge balance ANC. The model is calibrated to pH measurements (n = 322) by adjusting the fraction of active organic matter only, which results in an error of pH prediction on average below 0.2 pH units. The small systematic discrepancy between the analytical results for the monomeric aluminum fractionation and the model results is corrected for separately for two different fractionation techniques (n = 499) and validated on a large number (n = 3419) of geographically widely spread samples all over Sweden. The resulting average error for inorganic monomeric aluminum is around 1 µM. In its present form the model is the first internally consistent modeling approach for Sweden and may now be used as a tool for environmental quality management. Soil gibbsite with a log *Ks of 8.29 at 25°C together with a pH dependent loading function that uses molar Al/C ratios describes the amount of aluminum in solution in the presence of organic matter if the pH is roughly above 6.0.

Microbial reduction of 99Tc in organic matter-rich soils

International Nuclear Information System (INIS)

Abdelouas, A.; Grambow, B.; Fattahi, M.; Andres, Y.; Leclerc-Cessac, E.

2005-01-01

For safety assessment purposes, it is necessary to study the mobility of long-lived radionuclides in the geosphere and the biosphere. Within this framework, we studied the behaviour of 99 Tc in biologically active organic matter-rich soils. To simulate the redox conditions in soils, we stimulated the growth of aerobic and facultative denitrifying and anaerobic sulphate-reducing bacteria (SRB). In the presence of either a pure culture of denitrifiers (Pseudomonas aeruginosa) or a consortium of soil denitrifiers, the solubility of TcO 4 - was not affected. The nonsorption of TcO 4 - onto bacteria was confirmed in biosorption experiments with washed cells of P. aeruginosa regardless of the pH. At the end of denitrification with indigenous denitrifiers in soil/water batch experiments, the redox potential (E H ) dropped and this was accompanied by an increase of Fe concentration in solution as a result of reduction of less soluble Fe(III) to Fe(II) from the soil particles. It is suggested that this is due to the growth of a consortium of anaerobic bacteria (e.g., Fe-reducing bacteria). The drop in E H was accompanied by a strong decrease in Tc concentration as a result of Tc(VII) reduction to Tc(IV). Thermodynamic calculations suggested the precipitation of TcO 2 . The stimulation of the growth of indigenous sulphate-reducing bacteria in soil/water systems led to even lower E H with final Tc concentration of 10 -8 M. Experiments with glass columns filled with soil reproduced the results obtained with batch cultures. Sequential chemical extraction of precipitated Tc in soils showed that this radionuclide is strongly immobilised within soil particles under anaerobic conditions. More than 90% of Tc is released together with organic matter (60-66%) and Fe-oxyhydroxides (23-31%). The present work shows that ubiquitous indigenous anaerobic bacteria in soils play a major role in Tc immobilisation. In addition, organic matter plays a key role in the stability of the reduced Tc

ORGANIC MATTER AND CRUDE PROTEIN DEGRADATION SYNCHRONY IN DIETS SELECTED BY RANGE GOATS.

Directory of Open Access Journals (Sweden)

Rafael Ramírez Orduña

2010-09-01

Full Text Available The study was carried out with the aim to asses the synchrony of organic matter and crude protein degradation in the rumen of diets selected by range goats through two years. Five esophageal cannulated adult male goats were used to collect extrusa samples during summer (August 9–13 and autumn (November 29 –December 3 of 2006, winter (February 20 – 24, spring (April 29 –May 5, summer (September 10–15 and autumn (December 4–8 of 2007 and winter (February 20 – 25 and spring (May 9 –13 of 2008. Extrusa samples were subjected to chemical analysis to determine organic matter (OM, crude protein (CP in situ and in vitro true digestibility of dry matter. OM and CP intake were estimated by total fecal collection. Effective extent of degradation of the OM and CP was calculated hourly and total 24 hours. From the hourly quantity of OM and CP degraded, a synchrony index of CP to OM was calculated, and from the total 24 hours degradation, degraded organic matter intake and crude protein intake were also estimated. Sampling date was the main effect that determined the variation of diet OM and CP degradation parameters. Degraded crude protein intake as a proportion of degraded OM was affected by sampling date and was correlated to rainfall. During winter of the first year degraded crude protein intake was below the requirements for maintenance or to promote growth for range goats weighing 40 kg. Even though, synchrony index between OM and CP degradation was affected by sampling date goats maintained a high synchrony index throughout the years.

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

Science.gov (United States)

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

2017-12-01

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

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

Mass spectral chemical fingerprints reveal the molecular dependence of exhaust particulate matters on engine speeds.

Science.gov (United States)

Li, Yi; Zhang, Hua; Zhao, Zongshan; Tian, Yong; Liu, Kun; Jie, Feifan; Zhu, Liang; Chen, Huanwen

2018-05-01

Particulate matters (PMs) emitted by automobile exhaust contribute to a significant fraction of the global PMs. Extractive atmospheric pressure chemical ionization mass spectrometry (EAPCI-MS) was developed to explore the molecular dependence of PMs collected from exhaust gases produced at different vehicle engine speeds. The mass spectral fingerprints of the organic compounds embedded in differentially sized PMs (e.g., 0.22-0.45, 0.45-1.00, 1.00-2.00, 2.00-3.00, 3.00-5.00, and 5.00-10.00μm) generated at different engine speeds (e.g., 1000, 1500, 2000, 2500, and 3000r/min) were chemically profiled in the mass range of mass to charge ratio (m/z) 50-800. Organic compounds, including alcohols, aldehydes, and esters, were detected in all the PMs tested, with varied concentration levels for each individual PM sample. At relatively low engine speeds (≤1500r/min), the total amount of organic species embedded in PMs of 0.22-1.00μm was greater than in PMs of other sizes, while more organic species were found in PMs of 5.00-10.00μm at high engine speeds (≥3000r/min), indicating that the organic compounds distributed in different sizes of PMs strongly correlated with the engine speed. The experimental data showed that the EAPCI-MS technique enables molecular characterization of PMs in exhaust, revealing the chemical dependence of PMs on the engine speeds (i.e., the combustion conditions) of automobiles. Copyright © 2017. Published by Elsevier B.V.

Linking groundwater dissolved organic matter to sedimentary organic matter from a fluvio-lacustrine aquifer at Jianghan Plain, China by EEM-PARAFAC and hydrochemical analyses.

Science.gov (United States)

Huang, Shuang-bing; Wang, Yan-xin; Ma, Teng; Tong, Lei; Wang, Yan-yan; Liu, Chang-rong; Zhao, Long

2015-10-01

The sources of dissolved organic matter (DOM) in groundwater are important to groundwater chemistry and quality. This study examined similarities in the nature of DOM and investigated the link between groundwater DOM (GDOM) and sedimentary organic matter (SOM) from a lacustrine-alluvial aquifer at Jianghan Plain. Sediment, groundwater and surface water samples were employed for SOM extraction, optical and/or chemical characterization, and subsequent fluorescence excitation-emission matrix (EEM) and parallel factor analyses (PARAFAC). Spectroscopic properties of bulk DOM pools showed that indices indicative of GDOM (e.g., biological source properties, humification level, aromaticity and molecule mobility) varied within the ranges of those of two extracted end-members of SOM: humic-like materials and microbe-associated materials. The coexistence of PARAFAC compositions and the sustaining internal relationship between GDOM and extracted SOM indicate a similar source. The results from principal component analyses with selected spectroscopic indices showed that GDOM exhibited a transition trend regarding its nature: from refractory high-humification DOM to intermediate humification DOM and then to microbe-associated DOM, with decreasing molecular weight. Correlations of spectroscopic indices with physicochemical parameters of the groundwater suggested that GDOM was released from SOM and was modified by microbial diagenetic processes. The current study demonstrated the associations of GDOM with SOM from a spectroscopic viewpoint and provided new evidence supporting SOM as the source of GDOM. Copyright © 2015 Elsevier B.V. All rights reserved.

Impact of organic carbon and nutrients mobilized during chemical oxidation on subsequent bioremediation of a diesel-contaminated soil

NARCIS (Netherlands)

Sutton, N.B.; Grotenhuis, J.T.C.; Rijnaarts, H.H.M.

2014-01-01

Remediation with in situ chemical oxidation (ISCO) impacts soil organic matter (SOM) and the microbial community, with deleterious effects on the latter being a major hurdle to coupling ISCO with in situ bioremediation (ISB). We investigate treatment of a diesel-contaminated soil with Fenton’s

Humification and nonhumification pathways of the organic matter stabilization in soil: A review

Science.gov (United States)

Semenov, V. M.; Tulina, A. S.; Semenova, N. A.; Ivannikova, L. A.

2013-04-01

Polymeric and supramolecular models of humic substances (HSs) are considered. It has been noted that the HSs in natural objects can simultaneously occur in the forms of macromolecular polymers and supramolecularly organized monomers; macromolecular polymers of HSs can have some properties of suprastructures or be associated into aggregates, and covalent bonds can be formed between the monomers of supramolecules. Mineral particles of soil act as catalysts in chemical reactions between individual compounds, sorbents of biomolecules, and a surface for self-assembling HSs. It is supposed that the combination of such physicochemical processes and phenomena in soil as cementation, charring, incrustation, occlusion, sedimentation, sorption, coagulation, flocculation, encapsulation, complexation, and intercalation, as well as the entrapment of macroorganic, particulate, and soluble organic substances in micropores, can be as important for the stabilization of organic matter as the interactions between biomolecules with the formation of HSs.

Spatiotemporal Characterization of Chromophoric Dissolved Organic Matter (CDOM) and CDOM-DOC Relationships for Highly Polluted Rivers

OpenAIRE

Sijia Li; Jiquan Zhang; Guangyi Mu; Hanyu Ju; Rui Wang; Danjun Li; Ali Hassan Shabbir

2016-01-01

Spectral characteristics of CDOM (Chromophoric dissolved organic matter) in water columns are a key parameter for bio-optical modeling. Knowledge of CDOM optical properties and spatial discrepancy based on the relationship between water quality and spectral parameters in the Yinma River watershed with in situ data collected from highly polluted waters are exhibited in this study. Based on the comprehensive index method, the riverine waters showed serious contamination; especially the chemical...

Tritium in organic matter around Krsko Nuclear Power Plant

International Nuclear Information System (INIS)

Kristof, Romana; Zorko, Benjamin; Kozar Logar, Jasmina; Kosenina, Suzana

2017-01-01

The aim of the research was to obtain first results of tritium in the organic matter of environmental samples in the vicinity of Krsko NPP. The emphasis was on the layout of suitable sampling network of crops and fruits in nearby agricultural area. Method for determination of tritium in organic matter in the form of Tissue Free Water Tritium (TFWT) and Organically Bound Tritium (OBT) has been implemented. Capabilities of the methods were tested on real environmental samples and its findings were compared to modeled activities of tritium from atmospheric releases and literature based results of TFWT and OBT. (author)

Characterization of dissolved organic matter in fogwater by excitation-emission matrix fluorescence spectroscopy

Science.gov (United States)

Birdwell, J.E.; Valsaraj, K.T.

2010-01-01

Dissolved organic matter (DOM) present in fogwater samples collected in southeastern Louisiana and central-eastern China has been characterized using excitation-emission matrix fluorescence spectroscopy. The goal of the study was to illustrate the utility of fluorescence for obtaining information on the large fraction of organic carbon in fogwaters (typically >40% by weight) that defies characterization in terms of specific chemical compounds without the difficulty inherent in obtaining sufficient fogwater volume to isolate DOM for assessment using other spectroscopic and chemical analyses. Based on the findings of previous studies using other characterization methods, it was anticipated that the unidentified organic carbon fraction would have characteristic peaks associated with humic substances and fluorescent amino acids. Both humic- and protein-like fluorophores were observed in the fogwater spectra and fluorescence-derived indices for the fogwater had similar values to those of soil and sediment porewater. Greater biological character was observed in samples with higher organic carbon concentrations. Fogwaters are shown to contain a mixture of terrestrially- and microbially-derived fluorescent organic material, which is expected to be derived from an array of different sources, such as suspended soil and dust particles, biogenic emissions and organic substances generated by atmospheric processes. The fluorescence results indicate that much of the unidentified organic carbon present in fogwater can be represented by humic-like and biologically-derived substances similar to those present in other aquatic systems, though it should be noted that fluorescent signatures representative of DOM produced by atmospheric processing of organic aerosols may be contributing to or masked by humic-like fluorophores. ?? 2010.

[Vermicomposting of different organic materials and three-dimensional excitation emission matrix fluorescence spectroscopic characterization of their dissolved organic matter].

Science.gov (United States)

Yang, Wei; Wang, Dong-sheng; Liu, Man-qiang; Hu, Feng; Li, Hui-xin; Huang, Zhong-yang; Chang, Yi-jun; Jiao, Jia-guo

2015-10-01

In this experiment, different proportions of the cattle manure, tea-leaf, herb and mushroom residues, were used as food for earthworm (Eisenia fetida) to study the growth of the earth-worm. Then the characteristics and transformation of nutrient content and three-dimensional excitation emission matrix fluorescence (3DEEM) of dissolved organic matter (DOM) during vermistabilization were investigated by means of chemical and spectroscopic methods. The result showed that the mixture of different ratios of cattle manure with herb residue, and cattle manure with tea-leaf were conducive to the growth of earthworm, while the materials compounded with mushroom residue inhibited the growth of earthworm. With the increasing time of verimcomposting, the pH in vermicompost tended to be circumneutral and weakly acidic, and there were increases in electrical conductivity, and the contents of total nitrogen, total phosphorus, available nitrogen, and available phosphorus, while the total potassium and available potassium increased first and then decreased, and the organic matter content decreased. 3DEEM and fluorescence regional integration results indicated that, the fluorescence of protein-like fluorescence peaks declined significantly, while the intensity of humic-like fluorescence peak increased significantly in DOM. Vermicomposting process might change the compositions of DOM with elevated concentrations of humic acid and fulvic acid in the organics. In all, this study suggested the suitability of 3DEEM for monitoring the organics transformation and assessing the maturity in the vermicomposting.

Effect of radio-oxidative ageing and pH on the release of soluble organic matter from bitumen

International Nuclear Information System (INIS)

Libert, M.F.; Walczak, I.

2000-01-01

Bitumen is employed as an embedding matrix for low and medium level radioactive wastes. An high impermeability and a great resistance against most of chemicals are two of main bitumen properties. These characteristics of bitumen confinement properties may be modified under environmental parameters during intermediate storage or deep repository such as radiations or the presence of water. The radio-oxidation induces an increase of the quantity of leached organic matter. The evolution of the soluble organic species release seems to be linear with the irradiation dose, as soon as the dose is higher than 20 kGy, and seems to be no dependant of the dose rate. The generation of water-soluble organic complexing agents can affect the integrity of the wasteform due to an increase of the radionuclides solubility. An increase of the quantity of leached organic matter is also observed in presence of alkaline solutions. Identified molecules, by GC/MS analysis, are aromatics like naphthalene, oxidised compounds like alcohols, linear carbonyls, aromatics, glycols and nitrogen compounds. (authors)

Submicron particulate organic matter in the urban atmosphere: a new method for real-time measurement, molecular-level characterization and source apportionment

Science.gov (United States)

Müller, Markus; Eichler, Philipp; D'Anna, Barbara; Tan, Wen; Wisthaler, Armin

2017-04-01

We used a novel chemical analytical method for measuring submicron particulate organic matter in the atmosphere of three European cities (Innsbruck, Lyon, Valencia). Proton-Transfer-Reaction Time-of-Flight Mass Spectrometry (PTR-ToF-MS) was used in combination with the "chemical analysis of aerosol online" (CHARON) inlet for detecting particulate organic compounds on-line (i.e. without filter pre-collection), in real-time (1-min time resolution), at ng m-3 concentrations, with molecular-level resolution (i.e. obtaining molecular weight and elemental composition information). The CHARON-PTR-ToF-MS system monitored molecular tracers associated with different particle sources including levoglucosan from biomass combustion, PAHs from vehicular traffic, nicotine from cigarette smoking, and monoterpene oxidation products secondarily formed from biogenic emissions. The tracer information was used for interpreting positive matrix factorization (PMF) data which allowed us to apportion the sources of submicron particulate organic matter in the different urban environments. This work was funded through the PIMMS ITN, which was supported by the European Commission's 7th Framework Programme under grant agreement number 287382.

Radiation Dose Measurement Using Chemical Dosimeters

International Nuclear Information System (INIS)

Lee, Min Sun; Kim, Eun Hee; Kim, Yu Ri; Han, Bum Soo

2010-01-01

The radiation dose can be estimated in various ways. Dose estimates can be obtained by either experiment or theoretical analysis. In experiments, radiation impact is assessed by measuring any change caused by energy deposition to the exposed matter, in terms of energy state (physical change), chemical production (chemical change) or biological abnormality (biological change). The chemical dosimetry is based on the implication that the energy deposited to the matter can be inferred from the consequential change in chemical production. The chemical dosimetry usually works on the sample that is an aqueous solution, a biological matter, or an organic substance. In this study, we estimated absorbed doses by quantitating chemical changes in matter caused by radiation exposure. Two different chemical dosimeters, Fricke and ECB (Ethanol-Chlorobenzene) dosimeter, were compared in several features including efficacy as dose indicator and effective dose range

Composition and structure of natural organic matter through advanced nuclear magnetic resonance techniques

Directory of Open Access Journals (Sweden)

Dainan Zhang

2017-02-01

Full Text Available Abstract Natural organic matter (NOM plays important roles in biological, chemical, and physical processes within the terrestrial and aquatic ecosystem. Despite its importance, a clear and exhaustive knowledge on NOM chemistry still lacks. Aiming to prove that advanced solid-state 13C nuclear magnetic resonance (NMR techniques may contribute to fill such a gap, in this paper we reported relevant examples of its applicability to NOM components, such as biomass, deposition material, sediments, and kerogen samples. It is found that nonhydrolyzable organic carbons (NHC, chars, and polymethylene carbons are important in the investigated samples. The structure of each of the NHC fractions is similar to that of kerogens, highlighting the importance of selective preservation of NOM to the kerogen origin in the investigated aquatic ecosystems. Moreover, during the artificial maturation experiments of kerogen, the chemical and structural characteristics such as protonated aromatic, nonprotonated carbons, and aromatic cluster size play important roles in the origin and variation of nanoporosity during kerogen maturation. Graphical abstract NMR parameters of thermally stimulated kerogens

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.

Characteristics of dissolved organic matter following 20 years of peatland restoration

NARCIS (Netherlands)

Höll, B.S.; Fiedler, S.; Jungkunst, H.F.; Kalbitz, K.; Freibauer, A.; Drösler, M.; Stahr, K.

2009-01-01

The changes in the amounts and composition of dissolved organic matter (DOM) following long-term peat restoration are unknown, although this fraction of soil organic matter affects many processes in such ecosystems. We addressed this lack of knowledge by investigating a peatland in south-west

The ectomycorrhizal fungus Paxillus involutus converts organic matter in plant litter using a trimmed brown-rot mechanism involving Fenton chemistry

DEFF Research Database (Denmark)

Rineau, Francois; Roth, Doris; Shah, Firoz

2012-01-01

chemistry similar to that of brown-rot fungi. The set of enzymes expressed by Pa. involutus during the degradation of the organic matter was similar to the set of enzymes involved in the oxidative degradation of wood by brown-rot fungi. However, Pa. involutus lacked transcripts encoding extracellular...... the mycorrhizal fungi. To capture the nitrogen, the fungi must at least partly disrupt the recalcitrant organic matterprotein complexes within which the nitrogen is embedded. This disruption process is poorly characterized. We used spectroscopic analyses and transcriptome profiling to examine the mechanism...... by which the ectomycorrhizal fungus Paxillus involutus degrades organic matter when acquiring nitrogen from plant litter. The fungus partially degraded polysaccharides and modified the structure of polyphenols. The observed chemical changes were consistent with a hydroxyl radical attack, involving Fenton...

Redox chemistry and natural organic matter (NOM): Geochemists' dream, analytical chemists' nightmare

Science.gov (United States)

Macalady, Donald L.; Walton-Day, Katherine

2011-01-01

Natural organic matter (NOM) is an inherently complex mixture of polyfunctional organic molecules. Because of their universality and chemical reversibility, oxidation/reductions (redox) reactions of NOM have an especially interesting and important role in geochemistry. Variabilities in NOM composition and chemistry make studies of its redox chemistry particularly challenging, and details of NOM-mediated redox reactions are only partially understood. This is in large part due to the analytical difficulties associated with NOM characterization and the wide range of reagents and experimental systems used to study NOM redox reactions. This chapter provides a summary of the ongoing efforts to provide a coherent comprehension of aqueous redox chemistry involving NOM and of techniques for chemical characterization of NOM. It also describes some attempts to confirm the roles of different structural moieties in redox reactions. In addition, we discuss some of the operational parameters used to describe NOM redox capacities and redox states, and describe nomenclature of NOM redox chemistry. Several relatively facile experimental methods applicable to predictions of the NOM redox activity and redox states of NOM samples are discussed, with special attention to the proposed use of fluorescence spectroscopy to predict relevant redox characteristics of NOM samples.

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.

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.)

Selective Leaching of Dissolved Organic Matter From Alpine Permafrost Soils on the Qinghai-Tibetan Plateau

Science.gov (United States)

Wang, Yinghui; Xu, Yunping; Spencer, Robert G. M.; Zito, Phoebe; Kellerman, Anne; Podgorski, David; Xiao, Wenjie; Wei, Dandan; Rashid, Harunur; Yang, Yuanhe

2018-03-01

Ongoing global temperature rise has caused significant thaw and degradation of permafrost soils on the Qinghai-Tibetan Plateau (QTP). Leaching of organic matter from permafrost soils to aquatic systems is highly complex and difficult to reproduce in a laboratory setting. We collected samples from natural seeps of active and permafrost layers in an alpine swamp meadow on the QTP to shed light on the composition of mobilized dissolved organic matter (DOM) by combining optical measurements, ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectrometry, radiocarbon (14C), and solid-state 13C nuclear magnetic resonance spectroscopy. Our results show that even though the active layer soils contain large amounts of proteins and carbohydrates, there is a selective release of aromatic components, whereas in the deep permafrost layer, carbohydrate and protein components are preferentially leached during the thawing process. Given these different chemical characteristics of mobilized DOM, we hypothesize that photomineralization contributes significantly to the loss of DOM that is leached from the seasonally thawed surface layer. However, with continued warming, biodegradation will become more important since biolabile materials such as protein and carbohydrate are preferentially released from deep-layer permafrost soils. This transition in DOM leachate source and associated chemical composition has ramifications for downstream fluvial networks on the QTP particularly in terms of processing of carbon and associated fluxes.

Effects of organic, biological and chemical fertilizers on vegetative indices and essential oil content of coriander (Coriandrum sativum L.

Directory of Open Access Journals (Sweden)

M Aghhavani Shajari

2016-05-01

Full Text Available This experiment was conducted to study the effects of single and combined application of organic, biological and chemical fertilizers on qualitative and quantitative characteristics of vegetative part of coriander, (Coriandrum sativum L.. The experiment was carried out as split plot in time based on Complete Randomized Block Design with three replications and 12 treatments at Research Station, Faculty of Agriculture, Ferdowsi University of Mashhad, Iran, during growing season of 2010-2011. Treatments included: (1 mycorrhiza (Glomus mosseae, (2 biosulfur (Thiobacillus sp., (3 chemical fertilizer (NPK, (4 cow manure, (5 vermicompost, (6 mycorrhiza + chemical fertilizer, (7 mycorrhiza + cow manure, (8 mycorrhiza + vermicompost, (9 biosulfur + chemical fertilizer, (10 biosulfur + cow manure, (11 biosulfur + vermicompost and (12 control. Vegetative parts of coriander were cut at 5% of flowering stage in two dates (19 May and 5 June. Results showed that the highest plant height (28 cm and lateral branches (5.2 were obtained in combined application of biosulfur with cow manure treatment. The highest fresh and dry leaf weight, fresh and dry matter yield and stem dry matter weight were obtained in single application of chemical fertilizer. Single application of biosulfur increased leaf/stem ratio. The highest essential oil percentage and essential oil yield were observed in cow manure treatment (0.2% and 1753 g.ha-1, respectively. The maximum leaf/stem ratio were observed in the first cutting, while the highest lateral branches, stem fresh and dry matter yield, essential oil percentage and essential oil yield were obtained in second cut. Overall, results of this study showed that the plant vegetative yield increased by using chemical fertilizer, while essential oil percentage and essential oil yield of coriander were improved by using organic and biological fertilizers.

New Approaches in Soil Organic Matter Fluorescence; A Solid Phase Fluorescence Approach

Science.gov (United States)

Bowman, M. M.; Sanclements, M.; McKnight, D. M.

2017-12-01

Fluorescence spectroscopy is a well-established technique to investigate the composition of organic matter in aquatic systems and is increasingly applied to soil organic matter (SOM). Current methods require that SOM be extracted into a liquid prior to analysis by fluorescence spectroscopy. Soil extractions introduce an additional layer of complexity as the composition of the organic matter dissolved into solution varies based upon the selected extractant. Water is one of the most commonly used extractant, but only extracts the water-soluble fraction of the SOM with the insoluble soil organic matter fluorescence remaining in the soil matrix. We propose the use of solid phase fluorescence on whole soils as a potential tool to look at the composition of organic matter without the extraction bias and gain a more complete understand of the potential for fluorescence as a tool in terrestrial studies. To date, the limited applications of solid phase fluorescence have ranged from food and agriculture to pharmaceutical with no clearly defined methods and limitations available. We are aware of no other studies that use solid phase fluorescence and thus no clear methods to look at SOM across a diverse set of soil types and ecosystems. With this new approach to fluorescence spectroscopy there are new challenges, such as blank correction, inner filter effect corrections, and sample preparation. This work outlines a novel method for analyzing soil organic matter using solid phase fluorescence across a wide range of soils collected from the National Ecological Observatory Network (NEON) eco-domains. This method has shown that organic matter content in soils must be diluted to 2% to reduce backscattering and oversaturation of the detector in forested soils. In mineral horizons (A) there is observed quenching of the humic-like organic matter, which is likely a result of organo-mineral complexation. Finally, we present preliminary comparisons between solid and liquid phase

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

[Application of excitation-emission matrix spectrum combined with parallel factor analysis in dissolved organic matter in East China Sea].

Science.gov (United States)

Lü, Li-Sha; Zhao, Wei-Hong; Miao, Hui

2013-03-01

Using excitation-emission matrix spectrum(EEMs) combined with parallel factor analysis (PARAFAC) examine the fluorescent components feature of dissolved organic matter (DOM) sampled from East China Sea in the summer and autumn was examined. The type, distribution and origin of the fluorescence dissolved organic matter were also discussed. Three fluorescent components were identified by PARAFAC, including protein-like component C1 (235, 280/330), terrestrial or marine humic-like component C2 (255, 330/400) and terrestrial humic-like component C3 (275, 360/480). The good linearity of the two humic-like components showed the same source or some relationship between the chemical constitutions. As a whole, the level of the fluorescence intensity in coastal ocean was higher than that of the open ocean in different water layers in two seasons. The relationship of three components with chlorophyll-a and salinity showed the DOM in the study area is almost not influenced by the living algal matter, but the fresh water outflow of the Yangtze River might be the source of them in the Yangtze River estuary in Summer. From what has been discussed above, we can draw the conclusion that the application of EEM-PARAFAC modeling will exert a profound influence upon the research of the dissolved organic matter.

Multi-technical approach to characterize the dissolved organic matter from clay-stone

International Nuclear Information System (INIS)

Blanchart, Pascale; Michels, Raymond; Faure, Pierre; Parant, Stephane; Bruggeman, Christophe; De Craen, Mieke

2012-01-01

Document available in extended abstract form only. Currently, different clay formations (Boom Clay, Callovo-Oxfordian argilites, Opalinus Clay, Toarcian shales...) are studied as reference host rocks for methodological studies on the geological disposal of high-level and long-lived radioactive waste. While a significant effort is being done on the characterization of the mineral composition and the reactivity of the clays as barriers, the occurrence of organic matter, even in low proportion cannot be neglected. The organic matter appears as gas (C 1 -C 4 as identified in the Bure underground facilities), as solid (kerogen), as hydrocarbon liquids (free hydrocarbons within the kerogen or adsorbed on minerals) as well as in the aqueous phase (Dissolved Organic Matter - DOM). DOM raises specific interest, as it may have complexation properties towards metals and rare earth elements and is potentially mobile. Therefore, it is important to characterize the DOM as part of a study of feasibility of geological disposal. In this study, four host rocks were studied: - The Callovo-Oxfordian shales of Bure Underground Research Laboratory (Meuse, France); - The Opalinus Clay of Mont Terri Underground Research Laboratory (Switzerland); - The Toarcian shales of Tournemire (Aveyron, France); - The Boom Clay formation studied in The HADES Underground Research Laboratory (Mol, Belgium). Organic matter characteristics vary upon formation in terms of (i) origin (mainly marine type II; mixtures of marine type II and higher plants type III organic matter often poorly preserved), (ii) TOC contents, (iii) thermal maturity (for instance, Opalinus Clay and Toarcian shales are more mature and have poor oxygen content compare to Callovo-Oxfordian shales and Boom Clay). These differences in organic matter quality may have an influence on the quantity and the quality of DOM. The DOM of the rocks was isolated by Soxhlet extraction using pure water. A quantitative and qualitative multi

Seasonal changes in the chemical quality and biodegradability of dissolved organic matter exported from soils to streams in coastal temperate rainforest watersheds

Science.gov (United States)

Jason B. Fellman; Eran Hood; David V. D' Amore; Richard T. Edwards; Dan White

2009-01-01

The composition and biodegradability of streamwater dissolved organic matter (DOM) varies with source material and degree of transformation. We combined PARAFAC modeling of fluorescence excitation-emission spectroscopy and biodegradable dissolved organic carbon (BDOC) incubations to investigate seasonal changes in the lability of DOM along a soil-stream continuum in...

The sorption characteristics of mercury as affected by organic matter content and/or soil properties

Science.gov (United States)

Šípková, Adéla; Šillerová, Hana; Száková, Jiřina

2014-05-01

The determination and description of the mercury sorption extend on soil is significant for potential environmental toxic effects. The aim of this study was to assess the effectiveness of mercury sorption at different soil samples and vermicomposts. Mercury interactions with soil organic matter were studied using three soils with different physical-chemical properties - fluvisol, cambisol, and chernozem. Moreover, three different vermicomposts based on various bio-waste materials with high organic matter content were prepared in special fermentors. First was a digestate, second was represented by a mixture of bio-waste from housing estate and woodchips, and third was a garden bio-waste. In the case of vermicompost, the fractionation of organic matter was executed primarily using the resin SuperliteTM DAX-8. Therefore, the representation of individual fractions (humic acid, fulvic acid, hydrophilic compounds, and hydrophobic neutral organic matter) was known. The kinetics of mercury sorption onto materials of interest was studied by static sorption experiments. Samples were exposed to the solution with known Hg concentration of 12 mg kg-1 for the time from 10 minutes to 24 hours. Mercury content in the solutions was measured by the inductively coupled plasma mass spectrometry (ICP-MS). Based on this data, the optimum conditions for following sorption experiments were chosen. Subsequently, the batch sorption tests for all soil types and vermicomposts were performed in solution containing variable mercury concentrations between 1 and 12 mg kg-1. Equilibrium concentration values measured in the solution after sorption and calculated mercury content per kilogram of the soil or the vermi-compost were plotted. Two basic models of sorption isotherm - Langmuir and Freundlich, were used for the evaluation of the mercury sorption properties. The results showed that the best sorption properties from studied soil were identified in chernozem with highest cation exchange

The Influence of Land-Use Change on Soil and Dissolved Organic Matter Age, Lability, and Chemical Characteristics in Brazilian Oxisols

Science.gov (United States)

James, J. N.; Harrison, R. B.; Gross, C. D.; Dwivedi, P.; Myers, T.; Butman, D. E.

2017-12-01

Recent advances in freshwater research indicate that the age of carbon exported from major rivers globally increases with greater human disturbance in the watershed. This implies that human land-use can release old, previously mineral-associated C into solution with subsequent export to groundwater and ultimately freshwater systems where terrestrial organic matter is either mineralized to CO2, stored in aquatic sediments, or exported to the ocean. It is important to understand the mechanisms that cause the release of mineral-bound soil organic matter (SOM) into solution in response to human disturbance and land-use change. To better characterize the response of the total soil organic matter (SOM) pool to disturbance, this study examines the interactions between dissolved and bulk soil pools in response to conversion of Brazilian Cerrado (savannah forest) to Eucalyptus plantations. Water-extractable organic matter (WEOM) was obtained from soil samples down to 150 cm at 4 sites in Sao Paulo State, Brazil. These WEOM samples were characterized using fluorescence and NMR spectroscopy, incubated to assess biolability, and carbon-dated. Simultaneously, bulk mineral soil samples were analyzed for microbial biomass, carbon content and age, and characterized using Fourier Transform Infrared Spectroscopy. FTIR spectra of SOM were obtained by washing subsamples with sodium hypochlorite and subtracting the subsequent mineral matrix spectra from bulk soil spectra. Preliminary results show that microbial biomass decreases much more quickly with depth than WEOM, suggesting that C released into solution from deeper horizons may be less likely to be intercepted, and thus preferentially leached to groundwater. Native Cerrado forests had substantially more roots compared to Eucalyptus, and also released substantially larger quantities of WEOM from their O horizons. Furthermore, the age of WEOM released under Eucalyptus forest was more similar in age to bulk SOM, while Cerrado forest

Release of iodine from organic matter in natural water by K2S2O8 oxidation for 129I determination

DEFF Research Database (Denmark)

Dang, Haijun; Hou, Xiaolin; Roos, Per

2013-01-01

Accelerator mass spectrometry is the only method for measuring 129I in low level environmental samples. In this method, it is essential to convert organic associated iodine into inorganic form for the determination of total 129I or organic 129I because AgI is usually adopted as a target for AMS...... measurement of 129I. The chemical oxidative method to release iodine from organic matter in natural water was investigated using anion exchange chromatography and CHCl3 extraction methods. K2S2O8 was confirmed to be an ideal oxidative reagent for decomposing organic matters and converting organic iodine...... to inorganic form. More than 95% of iodine in natural water can be separated by solvent extraction after oxidation under optimal conditions, and the isotopic exchange of iodine in inorganic and organic forms was well completed during the oxidation, being able to result in an identical 129I/127I ratio...

Laboratory simulated hydrothermal alteration of sedimentary organic matter from Guaymas Basin, Gulf of California. Ph.D. Thesis

Science.gov (United States)

Leif, Roald N.

1993-01-01

High temperature alteration of sedimentary organic matter associated with marine hydrothermal systems involves complex physical and chemical processes that are not easily measured in most natural systems. Many of these processes can be evaluated indirectly by examining the geochemistry of the hydrothermal system in the laboratory. In this investigation, an experimental organic geochemical approach to studying pyrolysis of sedimentary organic matter is applied to the hydrothermal system in the Guaymas Basin, Gulf of California. A general survey of hydrothermal oils and extractable organic matter (bitumen) in hydrothermally altered sediments identified several homologous series of alkanones associated with a high temperature hydrothermal origin. The alkanones range in carbon number from C11 to C30 with no carbon number preference. Alkan-2-ones are in highest concentrations, with lower amounts of 3-, 4-, 5- (and higher) homologs. The alkanones appear to be pyrolysis products synthesized under extreme hydrothermal conditions. Hydrous pyrolysis and confinement pyrolysis experiments were performed to simulate thermally enhanced diagenetic and catagenetic changes in the immature sedimentary organic matter. The extent of alteration was measured by monitoring the n-alkanes, acyclic isoprenoids, steroid and triterpenoid biomarkers, polycyclic aromatic hydrocarbons and alkanones. The results were compared to bitumen extracts from sediments which have been naturally altered by a sill intrusion and accompanied hydrothermal fluid flow. These pyrolysis experiments duplicated many of the organic matter transformations observed in the natural system. Full hopane and sterane maturation occurred after 48 hr in experiments at 330 deg C with low water/rock mass ratios (0.29). A variety of radical and ionic reactions are responsible for the organic compound conversions which occur under extreme hydrothermal conditions. Short duration pyrolysis experiments revealed that a portion of the

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

Cosorption study of organic pollutants and dissolved organic matter in a soil

Energy Technology Data Exchange (ETDEWEB)

Flores-Cespedes, F. [Department of Inorganic Chemistry, University of Almeria, La Canada de San Urbano s/n, 04120 Almeria (Spain); Fernandez-Perez, M. [Department of Inorganic Chemistry, University of Almeria, La Canada de San Urbano s/n, 04120 Almeria (Spain)]. E-mail: mfernand@ual.es; Villafranca-Sanchez, M. [Department of Inorganic Chemistry, University of Almeria, La Canada de San Urbano s/n, 04120 Almeria (Spain); Gonzalez-Pradas, E. [Department of Inorganic Chemistry, University of Almeria, La Canada de San Urbano s/n, 04120 Almeria (Spain)

2006-08-15

In this study we have evaluated the effects of dissolved organic matter (DOM) on sorption of imidacloprid, 3,4-dichloroaniline (3,4-DCA) and 4-bromoaniline (4-BA) on a typical calcareous soil (Luvic Xerosol) from south-eastern Spain. Two different types of DOM were used, that is to say, dissolved natural organic matter extracts from a commercial peat (DNOM) and a high-purity tannic acid (TA) solution. The experiments were carried out in a 0.01 M CaCl{sub 2} aqueous medium at 25 deg. C. The results indicated that the presence of both DNOM and TA, over a concentration range of 15-100 mg L{sup -1}, produced an increase in the amount of 3,4-DCA and 4-BA sorbed and a decrease in the amount of imidacloprid retained on the soil studied. A modified distribution coefficient, K {sub doc}, has been proposed as a safer parameter for soil sorption predictions of organic pollutants and it could be of help to model the fate of these in the environment. - Cosorption of organic pollutants and DOM.

Cosorption study of organic pollutants and dissolved organic matter in a soil

International Nuclear Information System (INIS)

Flores-Cespedes, F.; Fernandez-Perez, M.; Villafranca-Sanchez, M.; Gonzalez-Pradas, E.

2006-01-01

In this study we have evaluated the effects of dissolved organic matter (DOM) on sorption of imidacloprid, 3,4-dichloroaniline (3,4-DCA) and 4-bromoaniline (4-BA) on a typical calcareous soil (Luvic Xerosol) from south-eastern Spain. Two different types of DOM were used, that is to say, dissolved natural organic matter extracts from a commercial peat (DNOM) and a high-purity tannic acid (TA) solution. The experiments were carried out in a 0.01 M CaCl 2 aqueous medium at 25 deg. C. The results indicated that the presence of both DNOM and TA, over a concentration range of 15-100 mg L -1 , produced an increase in the amount of 3,4-DCA and 4-BA sorbed and a decrease in the amount of imidacloprid retained on the soil studied. A modified distribution coefficient, K doc , has been proposed as a safer parameter for soil sorption predictions of organic pollutants and it could be of help to model the fate of these in the environment. - Cosorption of organic pollutants and DOM

Test procedure for determining organic matter content in soils : UV-VIS method.

Science.gov (United States)

2010-11-01

The Texas Department of Transportation has been having problems with organic matter in soils that they : stabilize for use as subgrade layers in road construction. The organic matter reduces the effectiveness of : common soil additives (lime/cement) ...

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.

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.

The organization for the prohibition of chemical weapons and the IAEA: A comparative overview

International Nuclear Information System (INIS)

Dorn, A.W.; Rolya, A.

1993-01-01

The long-awaited Chemical Weapons Convention (CWC) - which was endorsed in New York by the United Nations General Assembly on 30 November 1992 - was opened for signature on 13 January 1993. To oversee its implementation, a new international organization, the Organization for the Prohibition of Chemical Weapons (OPCW), will be established when the treaty enters into force, which could be as early as January 1995. The IAEA - as the only existing organization with a mandate for implementing an international verification system - is an important model for the structure and functioning of the OPCW. Many provisions in the CWC benefit from the lessons learned through the implementation of the IAEA's safeguards system in such matters as rights of access for inspectors, the designation of inspectors, and procedural arrangements. Overall, the structure of the IAEA and that foreseen for the OPCE are quite similar. There are, nonetheless, several structural differences. Most notably, the IAEA is charged with a dual mission, that of promoting the contribution of nuclear energy to social and economic development and of seeking to ensure that nuclear materials and facilities which have been placed under safeguards are not diverted from peaceful uses. The OPCW is responsible for achieving a complete ban on chemical weapons and is not responsible, at least as currently envisaged, for the promotion of peaceful uses of chemistry and chemical sciences

Alteration of Chemical Composition of Soil-leached Dissolved Organic Matter under Cryogenic Cycles

Science.gov (United States)

Zhang, X.; Bianchi, T. S.; Schuur, E.

2016-02-01

Arctic permafrost thawing has drawn great attention because of the large amount of organic carbon (OC) storage in Arctic soils that are susceptible to increasing global temperatures. Due to microbial activities, some of the OC pool is converted in part to greenhouse gases, like CH4 and CO2 gas, which can result in a positive feedback on global warming. In Artic soils, a portion of OC can be mobilized by precipitation, drainage, and groundwater circulation which can in some cases be transported to rivers and eventually the coastal margins. To determine some of the mechanisms associated with the mobilization of OC from soils to aquatic ecosystems, we conducted a series of laboratory soil leaching experiments. Surface soil samples collected from Healy, Alaska were eluted with artificial rain at a constant rate. Leachates were collected over time and analyzed for dissolved organic carbon (DOC) concentrations. Concentrations began from 387-705 mg/L and then dropped to asymptote states to 25-219 mg/L. High-resolution spectroscopy was used to characterize colored dissolved organic matter (CDOM) and CDOM fluorescence intensity also dropped with time. Fluorescence maximum intensity (Fmax) for peak C ranged from 0.7-4.2 RU, with Exmax/Emmax = 310/450 nm. Fmax for peak T ranged from 0.5-3.2 RU, with Exmax/Emmax = 275/325 nm. Peak C: peak T values indicated preferential leaching of humic-like components over protein-like components. After reaching asymptotic levels, samples were stored frozen and then thawed to study the cryogenic impact on OC composition. CDOM intensity and DOC concentration increased after the freeze-thaw cycle. It was likely that cryogenic processes promoted the breakdown of OC and the releases of more DOC from soils. PARAFAC of CDOM excitation and emission matrices (EEMs) will be used to analyze CDOM composition of the soil leachates.

Differences in chemical composition of soil organic matter in natural ecosystems from different climatic regions: a pyrolysis-GC/MS study

NARCIS (Netherlands)

Vancampenhout, K.; Wouters, K.; Vos, de B.; Buurman, P.; Swennen, R.; Deckers, J.

2009-01-01

Soil organic matter (SOM) is a key factor in ecosystem dynamics. A better understanding of the global relationship between environmental characteristics, ecosystems and SOM chemistry is vital in order to assess its specific influence on carbon cycles. This study compared the composition of extracted

Accretion and Preservation of Organic Matter in Carbonaceous Chondrites as Revealed by NanoSIMS Imaging.

Science.gov (United States)

Remusat, L.; Guan, Y.; Eiler, J.

2008-12-01

Carbonaceous chondrites are the most primitive known meteorites. Their parent bodies accreted several discrete components of the early solar system: CAIs, other silicates, oxides, sulfides, ice, organics, and noble gases. Radioactive decay of short live radionucleides quickly heated these parent bodies and drove thermal metamorphism and aqueous alteration of their constituents. Despite this post-acretionary modification, at least some components of the organic matter in the carbaceous chondrites retained distinctive isotopic and molecular properties that may relate to their pre-acretionary origins in the protosolar nebula or in the molecular cloud that gave birth to it [1]. These processes that gave rise to early solar-system organic matter and the extent to which it was modified by parent body processes are still a matter of debate [2]. We have acquired NanoSIMS images of matrices of several CI, CM, CR and CV chondrites to document, in- situ, the distribution of organics and their textural and chemical relationships to co-existing inorganic components. Importantly, we performed these analyses on essentially unmodified fragments of matrix material pressed into indium, rather than on extracts, which have been the focus of most previous work on meteoritic organic matter. Specifically, we simultaneously collected H, D, 12C, 18O, 26CN, 28Si and 32S with a spatial resolution of 200 nm. Inorganic constituents of the imaged domains were determined by SEM imaging and EDS analysis. We identify two textural classes of organic constituents: diffuse organic matter and organic particles ~ 1 micron in diameter. The particles are common and do not exhibit any textural association with any inorganic matrix constituent. This distribution is consistent with previous observations by fluorescence optical microscopy [3]. These organic particles are likely primarily composed of insoluble organic matter (IOM) that grew prior to accretion as pure organic particules and was preserved in

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.

Supramolecular chemistry: from molecular information towards self-organization and complex matter

International Nuclear Information System (INIS)

Lehn, Jean-Marie

2004-01-01

Molecular chemistry has developed a wide range of very powerful procedures for constructing ever more sophisticated molecules from atoms linked by covalent bonds. Beyond molecular chemistry lies supramolecular chemistry, which aims at developing highly complex chemical systems from components interacting via non-covalent intermolecular forces. By the appropriate manipulation of these interactions, supramolecular chemistry became progressively the chemistry of molecular information, involving the storage of information at the molecular level, in the structural features, and its retrieval, transfer, and processing at the supramolecular level, through molecular recognition processes operating via specific interactional algorithms. This has paved the way towards apprehending chemistry also as an information science. Numerous receptors capable of recognizing, i.e. selectively binding, specific substrates have been developed, based on the molecular information stored in the interacting species. Suitably functionalized receptors may perform supramolecular catalysis and selective transport processes. In combination with polymolecular organization, recognition opens ways towards the design of molecular and supramolecular devices based on functional (photoactive, electroactive, ionoactive, etc) components. A step beyond preorganization consists in the design of systems undergoing self-organization, i.e. systems capable of spontaneously generating well-defined supramolecular architectures by self-assembly from their components. Self-organization processes, directed by the molecular information stored in the components and read out at the supramolecular level through specific interactions, represent the operation of programmed chemical systems. They have been implemented for the generation of a variety of discrete functional architectures of either organic or inorganic nature. Self-organization processes also give access to advanced supramolecular materials, such as

Influence of particle characteristics and organic matter content on the bioavailability and bioaccumulation of pyrene by clams

International Nuclear Information System (INIS)

Verrengia Guerrero, N.R.; Taylor, M.G.; Wider, E.A.; Simkiss, K.

2003-01-01

An experimental model with artificial particles and humic acids describes bioavailability of sediment-bound pyrene to clams. - Hydrophobic chemicals are known to associate with sediment particles including those from both suspended particulate matter and bottom deposits. The complex and variable composition of natural particles makes it very difficult therefore, to predict the bioavailability of sediment-bound contaminants. To overcome these problems we have previously devised a test system using artificial particles, with or without humic acids, for use as an experimental model of natural sediments. In the present work we have applied this experimental technique to investigate the bioavailability and bioaccumulation of pyrene by the freshwater fingernail clam Sphaerium corneum. The uptake and accumulation of pyrene in clams exposed to the chemical in the presence of a sample of natural sediment was also investigated. According to the results obtained, particle surface properties and organic matter content are the key factors for assessing the bioavailability and bioaccumulation of pyrene by clams

Understanding dissolved organic matter reactivity in a global context: tribute to Dr. George Aiken's many contributions

Science.gov (United States)

McKnight, Diane

2017-04-01

As Dr. George Aiken emphasized throughout his distinguished research career, the diversity of sources of dissolved organic material (DOM) is associated with a diversity of dissolved organic compounds with a range of chemistries and reactivities that are present in the natural environment. From a limnological perspective, dissolved organic matter (DOM) can originate from allochthonous sources on the landscape which drains into a lake, river, wetland, coastal region, or other aquatic ecosystem, or from autochthonous sources within the given aquatic ecosystem. In many landscapes, the precursor organic materials that contribute to the DOM of the associated aquatic ecosystem can be derived from diverse sources, e.g. terrestrial plants, plant litter, organic material in different soil horizons, and the products of microbial growth and decay. Yet, through his focus on the underlying chemical processes a clear, chemically robust foundation for understanding DOM reactivity has emerged from Aiken's research. These processes include the enhancement in solubility due to ionized carboxylic acid functional groups and the reactions of organic sulfur groups with mercury. This approach has advanced understand of carbon cycling in the lakes of the Mars-like barren landscapes of the McMurdo Dry Valleys in Antarctica and the rivers draining the warming tundra of the Arctic.

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

Presence and evolution of natural organic matter in the boom clay

International Nuclear Information System (INIS)

Van Geet, M.; Deniau, I.; Largeau, C.; Bruggeman, C.; Maes, A.; Dierckx, A.

2004-01-01

Because of its very low hydraulic conductivity, reducing conditions, slightly alkaline pH, high specific surface, high cation exchange capacity and high plasticity, the Boom Clay is studied as a reference host formation for the deep disposal of high-level long-lived radioactive waste (NIRAS/ONDRAF, 1989). However, Boom Clay also contains up to 5% wt. of organic matter (OM). As radionuclides can form complexes with this organic matter, a detailed characterisation and knowledge of the evolution of the organic matter is necessary. An overview of the characteristics of the organic matter present in Boom Clay is given by Van Geet et al., (2003). The solid phase OM can be up to 5%. The dissolved OM fraction is around 200 mg C per liter of Boom Clay pore water. Both kinds of OM will be discussed. Concerning the solid phase OM the focus will be on the past evolution and its possible future evolution due to a thermal stress. For the dissolved OM, the focus will be on its origin. (author)

Organic matter in the universe

CERN Document Server

Kwok, Sun

2012-01-01

Authored by an experienced writer and a well-known researcher of stellar evolution, interstellar matter and spectroscopy, this unique treatise on the formation and observation of organic compounds in space includes a spectroscopy refresher, as well as links to geological findings and finishes with the outlook for future astronomical facilities and solar system exploration missions. A whole section on laboratory simulations includes the Miller-Urey experiment and the ultraviolet photolysis of ices.

Leader Election and Shape Formation with Self-Organizing Programmable Matter

OpenAIRE

Daymude, Joshua J.; Derakhshandeh, Zahra; Gmyr, Robert; Strothmann, Thim; Bazzi, Rida; Richa, Andréa W.; Scheideler, Christian

2015-01-01

We consider programmable matter consisting of simple computational elements, called particles, that can establish and release bonds and can actively move in a self-organized way, and we investigate the feasibility of solving fundamental problems relevant for programmable matter. As a suitable model for such self-organizing particle systems, we will use a generalization of the geometric amoebot model first proposed in SPAA 2014. Based on the geometric model, we present efficient local-control ...

Effects of exotic plantation forests on soil edaphon and organic matter fractions.

Science.gov (United States)

Xu, Gang; Liu, Yao; Long, Zhijian; Hu, Shanglian; Zhang, Yuanbin; Jiang, Hao

2018-06-01

There is uncertainty and limited knowledge regarding soil microbial properties and organic matter fractions of natural secondary forest accompanying chemical environmental changes of replacement by pure alien plantation forests in a hilly area of southwest of Sichuan province China. The aim of this study was to evaluate the impact of natural secondary forest (NSF) to pure Cryptomeria fortunei forest (CFF) and Cunninghamia lanceolata forest (CLF) on soil organic fractions and microbial communities. The results showed that the soil total phospholipid fatty acids (PLFAs), total bacteria and fungi, microbial carbon pool, organic recalcitrant carbon (C) and (N) fractions, soil microbial quotient and labile and recalcitrant C use efficiencies in each pure plantation were significantly decreased, but their microbial N pool, labile C and N pools, soil carbon dioxide efflux, soil respiratory quotient and recalcitrant N use efficiency were increased. An RDA analysis revealed that soil total PLFAs, total bacteria and fungi and total Gram-positive and Gram-negative bacteria were significantly associated with exchangeable Al 3+ , exchangeable acid, Al 3+ , available P and Mg 2+ and pH, which resulted into microbial functional changes of soil labile and recalcitrant substrate use efficiencies. Modified microbial C- and N-use efficiency due to forest conversion ultimately meets those of rapidly growing trees in plantation forests. Enlarged soil labile fractions and soil respiratory quotients in plantation forests would be a potential positive effect for C source in the future forest management. Altogether, pure plantation practices could provoke regulatory networks and functions of soil microbes and enzyme activities, consequently leading to differentiated utilization of soil organic matter fractions accompanying the change in environmental factors. Copyright © 2018 Elsevier B.V. All rights reserved.

Non-invasive localization of organic matter in soil aggregates using SR-μCT

Science.gov (United States)

Peth, Stephan; Mordhorst, Anneka; Chenu, Claire; Uteau Puschmann, Daniel; Garnier, Patricia; Nunan, Naoise; Pot, Valerie; Beckmann, Felix; Ogurreck, Malte

2014-05-01

Knowledge of the location of soil organic matter (SOM) and its spatial association to soil structure is an important step in improving modeling approaches for simulating organic matter turnover processes. Advanced models for carbon mineralization are able to account for the 3D distribution of SOM which is assumed to influence mineralisation. However, their application is still limited by the fact that no method exists to non-invasively determine the 3D spatial distribution of SOM in structured soils. SR-based X-ray microtomography (SR-µCT) is an advanced and promising tool in gaining knowledge on the 3-dimensional organization of soil phases (minerals, organic matter, water, air) which on a voxel level could be implemented into spatially explicit models. However, since the contrast of linear attenuation coefficients of soil organic matter on the one hand and mineral components and water on the other hand are relatively low, especially when materials are finely dispersed, organic matter within the soil pore space is often not resolved in ordinary X-ray absorption contrast imaging. To circumvent this problem we have developed a staining procedure for organic matter using Osmium-tetroxide since Osmium is an element with an absorption edge at a higher X-ray energy level. Osmium is known from transmission electron microscopy analysis (TEM) to stain organic matter specifically and irreversibly while having an absorption edge at approximately 74 keV. We report on the application of a novel Osmium vapor staining method to analyze differences in organic matter content and identify small scale spatial distribution of SOM in soil aggregates. To achieve this we have taken soil aggregate samples (6-8 mm across) obtained from arable soils differing in soil management. Aggregate samples were investigated by synchrotron-based X-ray microtomography (SR-µCT) after staining the sample with Osmium-tetroxide (OsO4) vapor. We utilized the monochromatic X-ray beam to locate osmium

Source and Processes of Dissolved Organic Matter in a Bangladesh Groundwater

Science.gov (United States)

McKnight, D. M.; Simone, B. E.; Mladenov, N.; Zheng, Y.; Legg, T. M.; Nemergut, D.

2010-12-01

Arsenic contamination of groundwater is a global health crisis, especially in Bangladesh where an estimated 40 million people are at risk. The release of geogenic arsenic bound to sediments into groundwater is thought to be influenced by dissolved organic matter (DOM) through several biogeochemical processes. Abiotically, DOM can promote the release of sediment bound As through the formation of DOM-As complexes and competitive interactions between As and DOM for sorption sites on the sediment. Additionally, the labile portion of groundwater DOM can serve as an electron donor to support microbial growth and the more recalcitrant humic DOM may serve as an electron shuttle, facilitating the eventual reduction of ferric iron present as iron oxides in sediments and consequently the mobilization of sorbed As and organic material. The goal of this study is to understand the source of DOM in representative Bangladesh groundwaters and the DOM sorption processes that occur at depth. We report chemical characteristics of representative DOM from a surface water, a shallow low-As groundwater, mid-depth high-As groundwater from the Araihazar region of Bangladesh. The humic DOM from groundwater displayed a more terrestrial chemical signature, indicative of being derived from plant and soil precursor materials, while the surface water humic DOM had a more microbial signature, suggesting an anthropogenic influence. In terms of biogeochemical processes occurring in the groundwater system, there is evidence from a diverse set of chemical characteristics, ranging from 13C-NMR spectroscopy to the analysis of lignin phenols, for preferential sorption onto iron oxides influencing the chemistry and reactivity of humic DOM in high As groundwater in Bangladesh. Taken together, these results provide chemical evidence for anthropogenic influence and the importance of sorption reactions at depth controlling the water quality of high As groundwater in Bangladesh.

Influence of N-15 labelled urea and azotobacter on corn yield and nitrogen budget as affected by organic matter

Energy Technology Data Exchange (ETDEWEB)

Soliman, S M; Abdelmonem, M A [Soil and Water Dept., Atomic Energy Authority, Cairo, (Egypt)

1995-10-01

As sandy soils of Egypt are poor in their chemical and physical properties, their fertilization with chemical or biological fertilizer is essential. The reported greenhouse experiment was conducted, using sandy soil of Egypt to evaluate the impact of urea fertilizer, applied alone combined with nitrification inhibitors (DCD) or (N-serve) on (corn yield and N-losses) as compared with inoculation with azotobacter under organic matter treatment as soil amendment. Total dry matter was recorded, while N-uptake by corn, and N-recovery due to inoculation with azotobacter was determined using N-15 dilution technique. Data obtained indicated that, application of DCD or N-serve with urea increased corn dry matter weight as well N-15 recovery. Significant increase in N-recovery was obtained due to nitrification inhibitor application and azotobacter inoculation. N-15 losses were reduced due to application of DCD and N-serve from 45% and respectively. Use of bio fertilizers and nitrification inhibitors could play an important role in corn production in sandy soil, as well as decrease the losses of applied N-fertilizers. fig., 3 tabs.

Influence of N-15 labelled urea and azotobacter on corn yield and nitrogen budget as affected by organic matter

International Nuclear Information System (INIS)

Soliman, S.M.; Abdelmonem, M.A.

1995-01-01

As sandy soils of Egypt are poor in their chemical and physical properties, their fertilization with chemical or biological fertilizer is essential. The reported greenhouse experiment was conducted, using sandy soil of Egypt to evaluate the impact of urea fertilizer, applied alone combined with nitrification inhibitors (DCD) or (N-serve) on (corn yield and N-losses) as compared with inoculation with azotobacter under organic matter treatment as soil amendment. Total dry matter was recorded, while N-uptake by corn, and N-recovery due to inoculation with azotobacter was determined using N-15 dilution technique. Data obtained indicated that, application of DCD or N-serve with urea increased corn dry matter weight as well N-15 recovery. Significant increase in N-recovery was obtained due to nitrification inhibitor application and azotobacter inoculation. N-15 losses were reduced due to application of DCD and N-serve from 45% and respectively. Use of bio fertilizers and nitrification inhibitors could play an important role in corn production in sandy soil, as well as decrease the losses of applied N-fertilizers. fig., 3 tabs

Effect of organic matter properties, clay mineral type and thermal maturity on gas adsorption in organic-rich shale systems

Science.gov (United States)

Zhang, Tongwei; Ellis, Geoffrey S.; Ruppel, Stephen C.; Milliken, Kitty; Lewan, Mike; Sun, Xun; Baez, Luis; Beeney, Ken; Sonnenberg, Steve

2013-01-01

A series of CH4 adsorption experiments on natural organic-rich shales, isolated kerogen, clay-rich rocks, and artificially matured Woodford Shale samples were conducted under dry conditions. Our results indicate that physisorption is a dominant process for CH4 sorption, both on organic-rich shales and clay minerals. The Brunauer–Emmett–Teller (BET) surface area of the investigated samples is linearly correlated with the CH4 sorption capacity in both organic-rich shales and clay-rich rocks. The presence of organic matter is a primary control on gas adsorption in shale-gas systems, and the gas-sorption capacity is determined by total organic carbon (TOC) content, organic-matter type, and thermal maturity. A large number of nanopores, in the 2–50 nm size range, were created during organic-matter thermal decomposition, and they significantly contributed to the surface area. Consequently, methane-sorption capacity increases with increasing thermal maturity due to the presence of nanopores produced during organic-matter decomposition. Furthermore, CH4 sorption on clay minerals is mainly controlled by the type of clay mineral present. In terms of relative CH4 sorption capacity: montmorillonite ≫ illite – smectite mixed layer > kaolinite > chlorite > illite. The effect of rock properties (organic matter content, type, maturity, and clay minerals) on CH4 adsorption can be quantified with the heat of adsorption and the standard entropy, which are determined from adsorption isotherms at different temperatures. For clay-mineral rich rocks, the heat of adsorption (q) ranges from 9.4 to 16.6 kJ/mol. These values are considerably smaller than those for CH4 adsorption on kerogen (21.9–28 kJ/mol) and organic-rich shales (15.1–18.4 kJ/mol). The standard entropy (Δs°) ranges from -64.8 to -79.5 J/mol/K for clay minerals, -68.1 to -111.3 J/mol/K for kerogen, and -76.0 to -84.6 J/mol/K for organic-rich shales. The affinity of CH4 molecules for sorption on organic matter

Evaluation of the production, composition and aluminum and iron complexation of algogenic organic matter

Czech Academy of Sciences Publication Activity Database

Pivokonský, Martin; Klouček, Ondřej; Pivokonská, Lenka

2006-01-01

Roč. 40, č. 16 (2006), s. 3045-3052 ISSN 0043-1354 R&D Projects: GA AV ČR KJB200600501 Institutional research plan: CEZ:AV0Z20600510 Keywords : affinity chromatography * algogenic organic matter * aluminum and iron coagulants * extracellular organic matter * molecular weight fractionation * intracellular organic matter Subject RIV: BK - Fluid Dynamics Impact factor: 2.459, year: 2006

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

Sorptive stabilization of organic matter by amorphous Al hydroxide

NARCIS (Netherlands)

Schneider, M.P.W.; Scheel, T.; Mikutta, R.; van Hees, P.; Kaiser, K.; Kalbitz, K.

2010-01-01

Amorphous Al hydroxides (am-Al(OH)(3)) strongly sorb and by this means likely protect dissolved organic matter (OM) against microbial decay in soils. We carried out batch sorption experiments (pH 4.5; 40 mg organic C L-1) with OM extracted from organic horizons under a Norway spruce and a European

Lability of Secondary Organic Particulate Matter

Energy Technology Data Exchange (ETDEWEB)

Liu, Pengfei; Li, Yong Jie; Wang, Yan; Giles, Mary K.; Zaveri, Rahul A.; Bertram, Allan K.; Martin, Scot T.

2016-10-24

Accurate simulations of the consenctrations of atmospheric organic particulate matter (PM) are needed for predicting energy flow in the Earth’s climate system. In the past, simulations of organic PM widely assume equilibrium partitioning of semivolatile organic compounds (SVOCs) between the PM and surrounding vapor. Herein, we test this assumption by measuring evaporation rates and associated vapor mass concentration of organic films representative of atmospheric PM. For films representing anthropogenic PM, evaporation rates and vapor mass concentrations increased above a threshold relative humidity (RH), indicating equilibrium partitioning above a transition RH but not below. In contrast for films representing biogenic PM, no threshold was observed, indicating equilibrium partitioning at all RHs. The results suggest that the mass lability of atmospheric organic PM can differ in consequential ways among Earth’s natural biomes, polluted regions, and regions of land-use change, and these differences need to be considered when simulating atmospheric organic PM.

Nitrogen-Bearing, Indigenous Carbonaceous Matter in the Nakhla Mars Meteorite

Science.gov (United States)

Thomas-Keprta, K. L.; Clemett, S. J.; Messenger, S.; Rahman, Z.; Gibson, E. K.; Wentworth, S. J.; McKay, D. S.

2017-01-01

We report the identification of discrete assemblages of nitrogen (N)-rich organic matter entrapped within interior fracture surfaces of the martian meteorite Nakhla. Based on context, composition and isotopic measurements this organic matter is of demonstrably martian origin. The presence of N-bearing organic species is of considerable importance to the habitable potential and chemical evolution of the martian regolith.

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

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.

Organic matter degradation drives benthic cyanobacterial mat abundance on Caribbean coral reefs.

Science.gov (United States)

Brocke, Hannah J; Polerecky, Lubos; de Beer, Dirk; Weber, Miriam; Claudet, Joachim; Nugues, Maggy M

2015-01-01

Benthic cyanobacterial mats (BCMs) are impacting coral reefs worldwide. However, the factors and mechanisms driving their proliferation are unclear. We conducted a multi-year survey around the Caribbean island of Curaçao, which revealed highest BCM abundance on sheltered reefs close to urbanised areas. Reefs with high BCM abundance were also characterised by high benthic cover of macroalgae and low cover of corals. Nutrient concentrations in the water-column were consistently low, but markedly increased just above substrata (both sandy and hard) covered with BCMs. This was true for sites with both high and low BCM coverage, suggesting that BCM growth is stimulated by a localised, substrate-linked release of nutrients from the microbial degradation of organic matter. This hypothesis was supported by a higher organic content in sediments on reefs with high BCM coverage, and by an in situ experiment which showed that BCMs grew within days on sediments enriched with organic matter (Spirulina). We propose that nutrient runoff from urbanised areas stimulates phototrophic blooms and enhances organic matter concentrations on the reef. This organic matter is transported by currents and settles on the seabed at sites with low hydrodynamics. Subsequently, nutrients released from the organic matter degradation fuel the growth of BCMs. Improved management of nutrients generated on land should lower organic loading of sediments and other benthos (e.g. turf and macroalgae) to reduce BCM proliferation on coral reefs.

Fixation and reduction of uranium by natural organic matter: reaction mechanisms and kinetics

International Nuclear Information System (INIS)

Nakashima, S.; Perruchot, A.; Trichet, J.; Disnar, J.R.

1987-01-01

The reactivity of lignite towards soluble uranyl species in an aqueous medium is experimentally investigated as a function of temperature (between 20 0 C and 400 0 C). The fixation process starts near 45 0 C, with reduction beginning around 120 0 C. The fixation process leads to the formation of chemically and thermally stable organo-uranyl species. The reduction of free uranyl species is accompanied by a stoichiometric (2:1) liberation of protons into the medium. These protons originate from the organic matter which thus undergoes dehydrogenation. The general evolution of the carbonaceous residue in the course of this reaction shows that alcoholic and aliphatic hydrocarbon groups are responsible for the reduction. This chemical dehydrogenation could explain the low hydrogen content of natural organic materials associated with uraniferous deposits. The kinetics of the reduction step have been studied at 180 0 C, 190 0 C and 200 0 C. The kinetic parameters determined over this temperature range, and the extrapolation made to 20 0 C, show that reduction can be a crucial process in the geochemical behaviour of uranium especially in the thermal conditions in which sedimentary basins evolve [fr

A ω-mercaptoundecylphosphonic acid chemically modified gold electrode for uranium determination in waters in presence of organic matter.

Science.gov (United States)

Merli, Daniele; Protti, Stefano; Labò, Matteo; Pesavento, Maria; Profumo, Antonella

2016-05-01

A chemically modified electrode (CME) on a gold surface assembled with a ω-phosphonic acid terminated thiol was investigated for its capability to complex uranyl ions. The electrode, characterized by electrochemical techniques, demonstrated to be effective for the determination of uranyl at sub-μgL(-1) level by differential pulse adsorptive stripping voltammetry (DPAdSV) in environmental waters, also in presence of humic matter and other potential chelating agents. The accuracy of the measurements was investigated employing as model probes ligands of different complexing capability (humic acids and EDTA). Copyright © 2016 Elsevier B.V. All rights reserved.

Characterization of Organic Matter under Different Pedoenvironments in the Viruá National Park, in Northern Amazon

Directory of Open Access Journals (Sweden)

José Frutuoso do Vale Júnior

2016-01-01

Full Text Available ABSTRACT Soil organic matter (SOM fractions result from a variety of environmental processes, which affect incorporation and production rates, decomposition, alteration, and/or mineralization of organic matter. The aim of this study was to characterize SOM under the environments of rain forest, wooded campinarana (grasslands, arboreal-shrubby campinarana, grassy-woody campinarana, and pioneer plants of the Viruá National Park, in the north of the Brazilian Amazon. After chemical and physical characterization and soil classification, total organic carbon (TOC, total N, microbial activity, organic C from fulvic acid fractions (FA, humic acid (HA, and humin (Hu were determined at two depths (0.00-0.15 and 0.15-0.30 m. The TOC was lower in the grassy-woody campinarana, arboreal-shrubby campinarana, and pioneer formation areas than in the rain forest. Higher values of microbial activity were related to forest ecosystems in soils without physical or water restrictions and with better fertility compared to the other areas. The Hu predominated in all vegetation types studied, especially in the surface layer, because of the more soluble nature of HA and FA; and the higher values of HA/FA ratios in wooded campinaranas indicate that these environments contribute to higher losses of humic substances through fulvic acid forms, due to better drainage conditions.

Toxic potential of organic constituents of submicron particulate matter (PM1) in an urban road site (Barcelona).

Science.gov (United States)

Mesquita, Sofia R; van Drooge, Barend L; Dall'Osto, Manuel; Grimalt, Joan O; Barata, Carlos; Vieira, Natividade; Guimarães, Laura; Piña, Benjamin

2017-06-01

Atmospheric particulate matter (PM) is a recognized risk factor contributing to a number of diseases in human populations and wildlife globally. Organic matter is a major component of PM, but its contribution to overall toxicity of PM has not been thoroughly evaluated yet. In the present work, the biological activity of organic extracts from PM1 (particles with less than 1 μm of aerodynamic diameter) collected from an urban road site in the centre of Barcelona (NE Spain) was evaluated using a yeast-based assay (AhR-RYA) and different gene expression markers in zebrafish embryos. Dioxin-like activity of the extracts correlated to primary emissions from local traffic exhausts, reflecting weekday/weekend alternance. Expression levels of cyp1a and of gene markers for key cellular processes and development (ier2, fos) also correlated to vehicle emissions, whereas expression of gene markers related to antioxidant defence and endocrine effects (gstal, hao1, ttr) was strongly reduced in samples with strong contribution from regional air masses with aged secondary organic species or with strong influence of biomass burning emissions. Our data suggest that the toxic potential of PM1 organic chemical constituents strongly depends on the emission sources and on the process of ageing from primary to secondary organic aerosols.

Preservation of labile organic matter in soils of drained thaw lakes in Northern Alaska

Science.gov (United States)

Mueller, Carsten W.; Rethemeyer, Janet; Kao-Kniffin, Jenny; Löppmann, Sebastian; Hinkel, Kenneth; Bockheim, James

2014-05-01

A large number of studies predict changing organic matter (OM) dynamics in arctic soils due to global warming. In contrast to rather slowly altering bulk soil properties, single soil organic matter (SOM) fractions can provide a more detailed picture of the dynamics of differently preserved SOM pools in climate sensitive arctic regions. By the study of the chemical composition of such distinctive SOM fractions using nuclear magnetic resonance spectroscopy (NMR) together with radiocarbon analyses it is possible to evaluate the stability of the major OM pools. Approximately 50-75% of Alaska's Arctic Coastal Plain is covered with thaw lakes and drained thaw lakes that follow a 5,000 yr cycle of development (between creation and final drainage), thus forming a natural soil chronosequence. The drained thaw lakes offer the possibility to study SOM dynamics affected by permafrost processes over millennial timescales. In April 2010 we sampled 16 soil cores (including the active and permanent layer) reaching from young drained lakes (0-50 years since drainage) to ancient drained lakes (3000-5500 years since drainage). Air dried soil samples from soil horizons of the active and permanent layer were subjected to density fractionation in order to differentiate particulate OM and mineral associated OM. The chemical composition of the SOM fractions was analyzed by 13C CPMAS NMR spectroscopy. For a soil core of a young and an ancient drained thaw lake basin we also analyzed the 14C content. For the studied soils we can show that up to over 25 kg OC per square meter are stored mostly as labile, easily degradable organic matter rich in carbohydrates. In contrast only 10 kg OC per square meter were sequestered as presumably more stable mineral associated OC dominated by aliphatic compounds. Comparable to soils of temperate regions, we found small POM (dating we could show the stabilization of younger more labile OM at greater depth in buried O horizons. Additionally the study of the

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

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.

Soil Organic Matter and Soil Productivity: Searching for the Missing Link

Science.gov (United States)

Felipe G. Sanchez

1998-01-01

Soil-organic matter (SOM) is a complex array of components including soil fauna and flora at different stages of decomposition (Berg et al., 1982). Its concentration in soils can vary from 0.5% in mineral soils to almost 100% in peat soils (Brady, 1974). Organic matter (OM) in the surface mineral soil is considered a major determinant of forest ecosystem productivity...

Influence of natural mobile organic matter on europium retention on Bure clay rock

International Nuclear Information System (INIS)

Vu-Do, Laurence

2013-01-01

Bure clay rock (CR) was chosen as host rock for the French high and intermediate level long lived radioactive waste repository. This choice is mostly explained by the retention ability of the Callovo-Oxfordian rock (COx). Bure clay rock contains natural organic matter (OM) that could have an influence on radionuclide retention. The aim of this work is to assess the influence of natural mobile OM on the retention of Eu on clay rock. Eu was chosen as a chemical model for trivalent actinides contained in vitrified waste. Three organic molecules were studied: suberic, sorbic and tiglic acids, small organic acids identified in COx pore water. All the experiments were carried out in an environment recreating COx water (pH=7.5; I=0.1 mol/L; PCO 2 =10 -2 bar).Clay rock sample characterization showed that the sample used in this work was similar to those previously extracted from the area of interest and that it was necessary to maintain pH at 7.5 to avoid altering the clay rock. The Eu-OM system study indicated that organic acids had no influence on Eu speciation in COx water. The Eu-CR system experimental study confirmed that retention implied sorption on CR (C(Eu)≤6.10 -6 mol/L) and precipitation in COx water (C(Eu)≥6.10 -6 mol/L). Distribution coefficient Rd (quantifying sorption) was estimated at 170 ± 30 L/g. This high value is consistent with literature values obtained on clay rocks. The ternary Eu-OM-CR system study showed a slight increase of sorption in the presence of organic matter. This synergistic effect is very satisfactory in terms of storage security: the presence of small organic acids in clay rock does not question retention properties with respect to europium and trivalent actinides. (author)

Fluorescence quantum yields of natural organic matter and organic compounds: Implications for the fluorescence-based interpretation of organic matter composition

DEFF Research Database (Denmark)

Wünsch, Urban; Murphy, Kathleen R.; Stedmon, Colin

2015-01-01

to more than 200 modeled spectra (PARAFAC components) in the OpenFluor database. Apparent matches, based on spectral similarity, were subsequently evaluated using molar fluorescence and absorbance. Five organic compounds were potential matches with PARAFAC components from 16 studies; however, the ability......Absorbance and fluorescence spectroscopy are economical tools for tracing the supply, turnover and fate of dissolved organic matter (DOM). The colored and fluorescent fractions of DOM (CDOM and FDOM, respectively) are linked by the apparent fluorescence quantum yield (AQY) of DOM, which reflects...... the likelihood that chromophores emit fluorescence after absorbing light. Compared to the number of studies investigating CDOM and FDOM, few studies have systematically investigated AQY spectra for DOM, and linked them to fluorescence quantum yields (Φ) of organic compounds. To offer a standardized approach...

Chemical characterization of soil organic matter in a Chesapeake Bay salt marsh: analyzing microbial and vegetation inputs to SOM

Science.gov (United States)

Bye, E.; Schreiner, K. M.; Abdulla, H. A.; Minor, E. C.; Guntenspergen, G. R.

2017-12-01

Coastal wetlands play a critical role in the global carbon cycle. These ecosystems sequester and store carbon, known as "blue carbon," at a rate two or three orders of magnitude larger than other terrestrial ecosystems, such as temperate, tropical, and boreal forests. Anthropogenic changes to the climate are threatening blue carbon stores in coastal wetland ecosystems. To understand and predict how these important carbon stores will be affected by anthropogenic climate changes, it is necessary to understand the formation and preservation of soil organic matter (SOM) in these ecosystems. This study will present organic geochemical data from two sediment cores collected from the Smithsonian Environmental Research Center site on a salt marsh in Maryland along the Chesapeake Bay. One core is from a location that recently transitioned from a C4 to C3 plant regime, currently dominated by the sedge Shoenplectis americanus. The second core is from a C4 plant (Spartina patens) dominated location in the marsh. The organic geochemistry of these 100 cm deep sediment cores was studied through multiple bulk analyses including stable isotopes, elemental ratios, Fourier-transform infrared spectroscopy (FTIR), solid-state magic-angle-spinning Nuclear Magnetic Resonance (NMR), and compound specific lignin-phenol analysis. By using comprehensive chemical characterization techniques, this study aims to discern between vegetation- and microbially-derived inputs to SOM in blue carbon ecosystems. The results show a general increase in the aromatic content with a concomitant decrease of carbohydrates with depth in both cores. However, substantial differences between the two cores, indicates differing inputs and/or stabilization mechanisms within SOM formed from different vegetation regimes. Further compound specific work will help to elucidate the specific source of compounds within each compound class, in surface and deep SOM, and additionally can help provide evidence for different

Fire Effects on Soil and Dissolved Organic Matter in a Southern Appalachian Hardwood Forest: Movement of Fire-Altered Organic Matter Across the Terrestrial-Aquatic Interface Following the Great Smoky Mountains National Park Fire of 2016

Science.gov (United States)

Matosziuk, L.; Gallo, A.; Hatten, J. A.; Heckman, K. A.; Nave, L. E.; Sanclements, M.; Strahm, B. D.; Weiglein, T.

2017-12-01

Wildfire can dramatically affect the quantity and quality of soil organic matter (SOM), producing thermally altered organic material such as pyrogenic carbon (PyC) and polyaromatic hydrocarbons (PAHs). The movement of this thermally altered material through terrestrial and aquatic ecosystems can differ from that of unburned SOM, with far-reaching consequences for soil carbon cycling and water quality. Unfortunately, due to the rapid ecological changes following fire and the lack of robust pre-fire controls, the cycling of fire-altered carbon is still poorly understood. In December 2016, the Chimney Tops 2 fire in Great Smoky Mountains National Park burned over co-located terrestrial and aquatic NEON sites. We have leveraged the wealth of pre-fire data at these sites (chemical, physical, and microbial characterization of soils, continuous measurements of both soil and stream samples, and five soil cores up to 110 cm in depth) to conduct a thorough study of the movement of fire-altered organic matter through terrestrial and aquatic ecosystems. Stream samples have been collected weekly beginning 5 weeks post-fire. Grab samples of soil were taken at discrete time points in the first two months after the fire. Eight weeks post-fire, a second set of cores was taken and resin lysimeters installed at three different depths. A third set of cores and grab samples will be taken 8-12 months after the fire. In addition to routine soil characterization techniques, solid samples from cores and grab samples at all time points will be analyzed for PyC and PAHs. To determine the effect of fire on dissolved organic matter (DOM), hot water extracts of these soil samples, as well as the stream samples and lysimeter samples, will also be analyzed for PyC and PAHs. Selected samples will be analyzed by 1D- and 2D-NMR to further characterize the chemical composition of DOM. This extensive investigation of the quantity and quality of fire-altered organic material at discrete time points

Effect of organic matter amendment, arsenic amendment and water management regime on rice grain arsenic species

International Nuclear Information System (INIS)

Norton, Gareth J.; Adomako, Eureka E.; Deacon, Claire M.; Carey, Anne-Marie; Price, Adam H.; Meharg, Andrew A.

2013-01-01

Arsenic accumulation in rice grain has been identified as a major problem in some regions of Asia. A study was conducted to investigate the effect of increased organic matter in the soil on the release of arsenic into soil pore water and accumulation of arsenic species within rice grain. It was observed that high concentrations of soil arsenic and organic matter caused a reduction in plant growth and delayed flowering time. Total grain arsenic accumulation was higher in the plants grown in high soil arsenic in combination with high organic matter, with an increase in the percentage of organic arsenic species observed. The results indicate that the application of organic matter should be done with caution in paddy soils which have high soil arsenic, as this may lead to an increase in accumulation of arsenic within rice grains. Results also confirm that flooding conditions substantially increase grain arsenic. -- Highlights: ► High soil arsenic and organic matter caused a reduction in plant growth. ► A delayed flowering time was observed in high arsenic and organic matter soil. ► Total grain arsenic increased in high arsenic and organic matter soil. ► Percentage organic arsenic in the grain altered in arsenic and organic matter soil. -- The addition of high amounts of organic matter to soils led to an increase in total rice grain arsenic, as well as alteration in the percentage arsenic species in the rice grains

Characterization of Soil Organic Matter in Peat Soil with Different Humification Levels using FTIR

Science.gov (United States)

Teong, I. T.; Felix, N. L. L.; Mohd, S.; Sulaeman, A.

2016-07-01

Peat soil is defined as an accumulation of the debris and vegetative under the water logging condition. Soil organic matter of peat soil was affected by the environmental, weather, types of vegetative. Peat soil was normally classified based on its level of humification. Humification can be defined as the transformation of numerous group of substances (proteins, carbohydrates, lipids, etc.) and individual molecules present in living organic matter into group of substances with similar properties (humic substances). During the peat transformation process, content of soil organic matter also will change. Hence, that is important to determine out the types of the organic compound. FTIR (Fourier Transform Infrared) is a machine which is used to differential soil organic matter by using infrared. Infrared is a types of low energy which can determine the organic minerals. Hence, FTIR can be suitable as an indicator on its level of humification. The main objective of this study is to identify an optimized method to characterization of the soil organic content in different level of humification. The case study areas which had been chosen for this study are Parit Sulong, Batu Pahat and UCTS, Sibu. Peat soil samples were taken by every 0.5 m depth until it reached the clay layer. However, the soil organic matter in different humification levels is not significant. FTIR is an indicator which is used to determine the types of soil, but it is unable to differentiate the soil organic matter in peat soil FTIR can determine different types of the soil based on different wave length. Generally, soil organic matter was found that it is not significant to the level of humification.

Soil architecture and distribution of organic matter

NARCIS (Netherlands)

Kooistra, M.J.; Noordwijk, van M.

1996-01-01

The biological component of soil structure varies greatly in quality and quantity, occurs on different scales, and varies throughout the year. It is far less predictable than the physical part and human impact. The occurrence and distribution of organic matter depends on several processes, related

A Robust Analysis Method For Δ13c Signal Of Bulk Organic Matter In Speleothems

Science.gov (United States)

Bian, F.; Blyth, A. J.; Smith, C.; Baker, A.

2017-12-01

Speleothems preserve organic matter that is derived from both the surface soil and cave environments. This organic matter can be used to understand paleoclimate and paleoenvironments. However, a stable and quick micro-analysis method to measure the δ13C signals from speleothem organic matter separate from the total δ13C remains absent. And speleothem organic geochemistry is still relatively unexplored compared to inorganic geochemistry. In this research, for the organic matter analysis, bulk homogeneous power samples were obtained from one large stalagmite. These were dissolved by phosphoric acid to produce the aqueous solution. Then, the processed solution was degassed through a rotational vacuum concentrator. A liquid chromatograph was coupled to IRMS to control the oxidization and the measurement of analytes. This method is demonstrated to be robust for the analysis of speleothem d13C organic matter analysis under different preparation and instrumental settings, with the low standard deviation ( 0.2‰), and low sample consumption (<25 mg). Considering the complexity of cave environments, this method will be useful in further investigations the δ13C of entrapped organic matter and environmental controls in other climatic and ecological contexts, including the determination of whether vegetation or soil microbial activity is the dominant control on speleothem d13C of organic matter.

Drugs as habitable planets in the space of dark chemical matter.

Science.gov (United States)

Siramshetty, Vishal B; Preissner, Robert

2018-03-01

A recent study demonstrated antifungal activity of dark chemical matter (DCM) compounds that were otherwise inactive in more than 100 HTS assays. These compounds were proposed to possess unique activity and 'clean' safety profiles. Here, we present an outlook of the promiscuity and safety of these compounds by retrospectively comparing their chemical and biological spaces with those of drugs. Significant amounts of marketed drugs (16%), withdrawn drugs (16.5%) and natural compounds (3.5%) share structural identity with DCM. Compound promiscuity assessment indicates that dark matter compounds could potentially interact with multiple biological targets. Further, thousands of DCM compounds showed presence of frequent-hitting pan-assay interference compound (PAINS) substructures. In light of these observations, filtering these compounds from screening libraries can be an irrevocable loss. Copyright © 2017 Elsevier Ltd. All rights reserved.

Formation of mercury sulfide from Hg(II)−thiolate complexes in natural organic matter

Science.gov (United States)

Alain Manceau,; Cyprien Lemouchi,; Mironel Enescu,; Anne-Claire Gaillot,; Martine Lanson,; Valerie Magnin,; Pieter Glatzel,; Poulin, Brett; Ryan, Joseph N.; Aiken, George R.; Isabelle Gautier-Lunea,; Kathryn L. Nagy,

2015-01-01

Methylmercury is the environmental form of neurotoxic mercury that is biomagnified in the food chain. Methylation rates are reduced when the metal is sequestered in crystalline mercury sulfides or bound to thiol groups in macromolecular natural organic matter. Mercury sulfide minerals are known to nucleate in anoxic zones, by reaction of the thiol-bound mercury with biogenic sulfide, but not in oxic environments. We present experimental evidence that mercury sulfide forms from thiol-bound mercury alone in aqueous dark systems in contact with air. The maximum amount of nanoparticulate mercury sulfide relative to thiol-bound mercury obtained by reacting dissolved mercury and soil organic matter matches that detected in the organic horizon of a contaminated soil situated downstream from Oak Ridge, TN, in the United States. The nearly identical ratios of the two forms of mercury in field and experimental systems suggest a common reaction mechanism for nucleating the mineral. We identified a chemical reaction mechanism that is thermodynamically favorable in which thiol-bound mercury polymerizes to mercury–sulfur clusters. The clusters form by elimination of sulfur from the thiol complexes via breaking of mercury–sulfur bonds as in an alkylation reaction. Addition of sulfide is not required. This nucleation mechanism provides one explanation for how mercury may be immobilized, and eventually sequestered, in oxygenated surface environments.

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).

ORGANIC CARBON AND TOTAL NITROGEN IN THE DENSIMETRIC FRACTIONS OF ORGANIC MATTER UNDER DIFFERENT SOIL MANAGEMEN

Directory of Open Access Journals (Sweden)

MARCELO RIBEIRO VILELA PRADO

2016-01-01

Full Text Available The evaluation of land use and management by the measurement of soil organic matter and its fractions has gained attention since it helps in the understanding of the dynamics of their contribution to soil productivity, especially in tropical environments. This study was conducted in the municipality of Colorado do Oeste, state of Rondônia, Brazil and its aim was to determinethe quantity of organic carbon and total nitrogen in the light and heavy fractions of organic matter in the surface layers of a typic hapludalf under different land use systems: Native Forest: open evergreen forest, reference environment; Agroforestry System 1: teak (Tectona grandis LF and kudzu (Pueraria montana; Agroforestry System 2: coffee (Coffea canephora, marandu palisade grass (Brachiaria brizantha cv. Marandu, “pinho cuiabano” (Parkia multijuga, teak and kudzu.; Agroforestry System 3: teak and cocoa (Theobroma cacao; Silvopasture System: teak, cocoa and marandu palisade grass; and Extensive Grazing System: marandu palisade grass. The experimental design was a randomized block in split-split plots (use systems versus soil layers of 0-0.05 and 0.05-0.10 m with three replications. The results showed that relative to Native Forest, the Agroforestry System 2 had equal- and greater amounts of organic carbon and total nitrogen respectively (light and heavy fractions in the soil organic matter, with the light fraction being responsible for storage of approximately 45% and 70% of the organic carbon and total nitrogen, respectively. Therefore, the light densimetric fraction proved to be useful in the early identification of the general decline of the soil organic matter in the land use systems evaluated.

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

Solid-state 13C nuclear magnetic resonance spectroscopic characterization of soil organic matter fractions in a forest ecosystem subjected to prescribed burning and thinning

Science.gov (United States)

Prescribed burning and thinning are gaining popularity as low-cost forest protection measures. Such field management practices could alter the chemical properties of soil organic matter (SOM), especially humic substances. In this work, we collected surface soil samples from the Bankhead National For...

Removal of nitrogen and organic matter in a submerged-membrane bioreactor operating in a condition of simultaneous nitrification and denitrification

Directory of Open Access Journals (Sweden)

Izabela Major Barbosa

2016-04-01

Full Text Available This study evaluated the removal of nitrogen and organic matter in a membrane bioreactor system operating in a condition of simultaneous nitrification and denitrification controlled by intermittent aeration. A submerged-membrane system in a bioreactor was used in a pilot scale to treat domestic wastewater. The dissolved oxygen concentration was maintained between 0.5 and 0.8 mg L-1. The concentration of the mixed liquor suspended solids (MLSS in the system ranged from 1 to 6 g L-1. The system efficiency was evaluated by the removal efficiency of organic matter, quantified by Chemical Oxygen Demand (COD, Biochemical Oxygen Demand (BOD5 and Total Organic Carbon (TOC. Nitrogen removal was assessed by quantifying Total Kjeldahl Nitrogen (TKN and ammonia nitrogen. During the system start-up, the removal efficiencies of COD and NTK were around 90% and 80%, respectively. After the simultaneous nitrification and denitrification (SND conditions were established, the removal efficiencies of COD and NTK were 70% and 99%, respectively. These results showed that sewage treatment with the membrane bioreactor (MBR system, operating with simultaneous nitrification and denitrification conditions, was able to remove organic matter and promote nitrification and denitrification in a single reactor, producing a high-quality permeate.

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

Cosorption study of organic pollutants and dissolved organic matter in a soil.

Science.gov (United States)

Flores-Céspedes, F; Fernández-Pérez, M; Villafranca-Sánchez, M; González-Pradas, E

2006-08-01

In this study we have evaluated the effects of dissolved organic matter (DOM) on sorption of imidacloprid, 3,4-dichloroaniline (3,4-DCA) and 4-bromoaniline (4-BA) on a typical calcareous soil (Luvic Xerosol) from south-eastern Spain. Two different types of DOM were used, that is to say, dissolved natural organic matter extracts from a commercial peat (DNOM) and a high-purity tannic acid (TA) solution. The experiments were carried out in a 0.01 M CaCl2 aqueous medium at 25 degrees C. The results indicated that the presence of both DNOM and TA, over a concentration range of 15-100 mg L(-1), produced an increase in the amount of 3,4-DCA and 4-BA sorbed and a decrease in the amount of imidacloprid retained on the soil studied. A modified distribution coefficient, K(doc), has been proposed as a safer parameter for soil sorption predictions of organic pollutants and it could be of help to model the fate of these in the environment.

Dependence of 210Po activity on organic matter in the reverine environs of coastal Kerala

International Nuclear Information System (INIS)

Narayana, Y.; Venunathan, N.

2011-01-01

This paper deals with the distribution of 210 Po in the river bank soil samples of three major rivers namely Bharathapuzha, Periyar and Kallada river of Kerala. The dependence of 210 Po activity on organic matter content in the samples was also studied. The soil samples were collected and analyzed for 210 Po radionuclide using standard radiochemical analytical method. Activity of 210 Po increases with increase in organic matter content in samples. Along the Bharathapuzha river bank the 210 Po activity ranges from 2.96 to 12.48 Bq kg -1 with mean 5.62 Bq kg -1 . The organic matter percentage in the samples ranges from 0.4 to 2.8 and a good correlation with correlation coefficient 0.9 was found between activity and organic matter percentage. In the Periyar river environs 210 Po activity ranges from 3.47 to 13.39 Bq kg -1 with mean value 9.27 Bq kg -1 . Organic matter percentage in these samples ranges from 1.20 to 4.10 and the correlation coefficient between 210 Po activity and organic matter percentage was found to be 0.8 In the Kallada river bank soil samples 210 Po activity ranges from 4.46 to 6.45 Bq kg -1 . The organic matter percentage ranges from 1.4 to 3. The correlation coefficient between 210 Po activity and organic matter percentage in the samples was found to be 0.9. (author)

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

International Nuclear Information System (INIS)

Ou Wenjia; Zhang Chengjun

2009-01-01

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

POM Pulses: Characterizing the Physical and Chemical Properties of Particulate Organic Matter (POM) Mobilized by Large Storm Events and its Influence on Receiving Fluvial Systems

Science.gov (United States)

Johnson, E. R.; Rowland, R. D.; Protokowicz, J.; Inamdar, S. P.; Kan, J.; Vargas, R.

2016-12-01

Extreme storm events have tremendous erosive energy which is capable of mobilizing vast amounts of material from watershed sources into fluvial systems. This complex mixture of sediment and particulate organic matter (POM) is a nutrient source, and has the potential to impact downstream water quality. The impact of POM on receiving aquatic systems can vary not only by the total amount exported but also by the various sources involved and the particle sizes of POM. This study examines the composition of POM in potential sources and within-event POM by: (1) determining the amount and quality of dissolved organic matter (DOM) that can be leached from coarse, medium and fine particle classes; (2) assessing the C and N content and isotopic character of within-event POM; and (3) coupling physical and chemical properties to evaluate storm event POM influence on stream water. Storm event POM samples and source sediments were collected from a forested headwater catchment (second order stream) in the Piedmont region of Maryland. Samples were sieved into three particle classes - coarse (2mm-1mm), medium (1mm-250µm) and fine (solid state event and source material. Future work will include examination of microbial communities associated with POM particle size classes. Physical size class separation of within-event POM exhibited differences in C:N ratios, δ15N composition, and extracted DOM lability. Smaller size classes exhibited lower C:N ratios, more enriched δ15N and more recalcitrant properties in leached DOM. Source material had varying C:N ratios and contributions to leached DOM. These results indicate that both source and size class strongly influence the POM contribution to fluvial systems during large storm events.

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...

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

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

Directory of Open Access Journals (Sweden)

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

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 NITROGEN TRANSFORMATIONS AND ROLE OF LIGHT FRACTION ORGANIC MATTER IN FOREST SOILS

Science.gov (United States)

Depletion of soil organic matter through cultivation may alter substrate availability for microbes, altering the dynamic balance between nitrogen (N) immobilization and mineralization. Soil light fraction (LF) organic matter is an active pool that decreases upon cultivation, and...

Turnover of intra- and extra-aggregate organic matter at the silt-size scale

Science.gov (United States)

I. Virto; C. Moni; C. Swanston; C. Chenu

2010-01-01

Temperate silty soils are especially sensitive to organic matter losses associated to some agricultural management systems. Long-term preservation of organic C in these soils has been demonstrated to occur mainly in the silt- and clay-size fractions, although our knowledge about the mechanisms through which it happens remains unclear. Although organic matter in such...

Elemental and isotopic characterization of organic particles in carbonaceous chondrites by NanoSIMS imaging: assessment on the origin, accretion and preservation of organic matter in chondrites

Science.gov (United States)

Remusat, L.; Guan, Y.; Eiler, J. M.

2009-12-01

Chondrites accreted primitive components, including organic compounds sampled from the proto-solar nebula. However, the molecular and isotopic fingerprints of organic matter extracted from chondrites are also potentially influenced by complex evolution on the parent bodies. We have performed NanoSIMS in situ characterisation of organic matter in the matrices of carbonaceous chondrites Orgueil (CI), Murchison (CM), Tagish Lake (C2), Renazzo (CR) and Allende (CV) with a spatial resolution of ~200 nm; we could also constrains textural relationships between organic constituents and other phases. Those meteorites have undergone a diverse set of parent body processes. I.e., CI, C2 and CM meteorites have undergone aqueous alteration, and the CV’s are thermally metamorphosed. The CR’s are inferred to be the least altered class of chondrites. Despite these differences in parent body modification, the distributions of organic carbon in these meteorites is similar: in all cases it can be found as micron-size, randomly distributed organic particles that are surrounded by the clay minerals that dominate the matrix material, but are not specifically associated with sulfides, sulfates or oxides. In addition, there is a “diffuse” fraction of organic carbon intimately associated with the clay-rich matrix. We hypothesize that the C particles we identify are hosts of insoluble organic matter that co-accreted with other primitive constituents of these materials, whereas the diffuse C fraction is the soluble component (i.e., soluble in laboratory organic and aqueous solvents). Our analytical technique lacks the spatial resolution required to analyze the diffuse organic matter without contamination by associated clays. But we are able to analyze the compositions of the interiors of relatively large C-rich particles (>500 nm) without such contamination. Some fraction of the C-rich particles in all of the examined meteorites but Allende exhibit a very high enrichment in deuterium

The Physics of Life. Part I: The Animate Organism as an Active Condensed Matter Body

OpenAIRE

Kukuruznyak , Dmitry ,

2017-01-01

Nonequilibrium "active agents" establish bonds with each other and create a quickly evolving condensed state known as active matter. Recently, active matter composed of motile self-organizing biopolymers demonstrated a biotic-like motion similar to cytoplasmic streaming. It was suggested that the active matter could produce cells. However, active matter physics cannot yet define an " organism " and thus make a satisfactory connection to biology. This paper describes an organism made of active...

Size distribution, chemical composition and oxidation reactivity of particulate matter from gasoline direct injection (GDI) engine fueled with ethanol-gasoline fuel

International Nuclear Information System (INIS)

Luo, Yueqi; Zhu, Lei; Fang, Junhua; Zhuang, Zhuyue; Guan, Chun; Xia, Chen; Xie, Xiaomin; Huang, Zhen

2015-01-01

Ethanol-gasoline blended fuels have been widely applied in markets recently, as ethanol reduces life-cycle greenhouse gas emissions and improves anti-knock performance. However, its effects on particulate matter (PM) emissions from gasoline direct injection (GDI) engine still need further investigation. In this study, the effects of ethanol-gasoline blended fuels on particle size distributions, number concentrations, chemical composition and soot oxidation activity of GDI engine were investigated. It was found that ethanol-gasoline blended fuels increased the particle number concentration in low-load operating conditions. In higher load conditions, the ethanol-gasoline was effective for reducing the particle number concentration, indicating that the chemical benefits of ethanol become dominant, which could reduce soot precursors such as large n-alkanes and aromatics in gasoline. The volatile organic mass fraction in ethanol-gasoline particulates matter was higher than that in gasoline particulate matter because ethanol reduced the amount of soot precursors during combustion and thereby reduced the elemental carbon proportions in PM. Ethanol addition also increased the proportion of small particles, which confirmed the effects of ethanol on organic composition. Ethanol-gasoline reduced the concentrations of most PAH species, except those with small aromatic rings, e.g., naphthalene. Soot from ethanol-gasoline has lower activation energy of oxidation than that from gasoline. The results in this study indicate that ethanol-gasoline has positive effects on PM emissions control, as the soot oxidation activity is improved and the particle number concentrations are reduced at moderate and high engine loads. - Highlights: • Ethanol-gasoline reduces elemental carbon in PM. • Ethanol-gasoline increases volatile organic fraction in PM. • Soot generated from ethanol-gasoline has higher oxidation activity.

Effect of selective removal of organic matter and iron oxides on the ...

African Journals Online (AJOL)

The effect of selective removal of organic matter and amorphous and crystalline iron oxides on N2-BET specific surface areas of some soil clays was evaluated. Clay fractions from 10 kaolinitic tropical soils were successively treated to remove organic matter by oxidation with Na hypochlorite, amorphous Fe oxide with acid ...

Mapping, organic matter mass and water volume of a peatland in Serra do Espinhaço Meridional

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José Ricardo da Rocha Campos

2012-06-01

Full Text Available Peatlands form in areas where net primary of organic matter production exceeds losses due to the decomposition, leaching or disturbance. Due to their chemical and physical characteristics, bogs can influence water dynamics because they can store large volumes of water in the rainy season and gradually release this water during the other months of the year. In Diamantina, Minas Gerais, Brazil, a peatland in the environmental protection area of Pau-de-Fruta ensures the water supply of 40,000 inhabitants. The hypothesis of this study is that the peat bogs in Pau-de-Fruta act as an environment for carbon storage and a regulator of water flow in the Córrego das Pedras basin. The objective of this study was to estimate the water volume and organic matter mass in this peatland and to study the influence of this environment on the water flow in the Córrego das Pedras basin. The peatland was mapped using 57 transects, at intervals of 100 m. Along all transects, the depth of the peat bog, the Universal Transverse Mercator (UTM coordinates and altitude were recorded every 20 m and used to calculate the area and volume of the peatland. The water volume was estimated, using a method developed in this study, and the mass of organic matter based on samples from 106 profiles. The peatland covered 81.7 hectares (ha, and stored 497,767 m³ of water, representing 83.7 % of the total volume of the peat bog. The total amount of organic matter (OM was 45,148 t, corresponding to 552 t ha-1 of OM. The peat bog occupies 11.9 % of the area covered by the Córrego das Pedras basin and stores 77.6 % of the annual water surplus, thus controlling the water flow in the basin and consequently regulating the water course.

pH dependence of steroid hormone-organic matter interactions at environmental concentrations

Energy Technology Data Exchange (ETDEWEB)

Neale, Peta A. [School of Engineering and Electronics, University of Edinburgh, Edinburgh, EH9 3JL (United Kingdom)], E-mail: p.neale@ed.ac.uk; Escher, Beate I. [Swiss Federal Institute of Aquatic Science and Technology (Eawag), 8600, Duebendorf (Switzerland); Schaefer, Andrea I. [School of Engineering and Electronics, University of Edinburgh, Edinburgh, EH9 3JL (United Kingdom)

2009-01-15

The interaction of estradiol, estrone, progesterone and testosterone with environmentally relevant concentrations of Aldrich humic acid, alginic acid and tannic acid was studied using solid-phase microextraction (SPME). Since bulk organic matter and certain hormones such as estradiol and estrone contain dissociable functional groups, the effect of pH on sorption was investigated as this will influence their fate and bioavailability. For humic acid and tannic acid, sorption was strongest at acidic pH when the bulk organic matter was in a non-dissociated form and decreased when they became partially negatively charged. At acidic and neutral pH the strength of partitioning was influenced by hormone functional groups content, with the strongest sorption observed for progesterone and estrone. At alkaline pH conditions, when the bulk organics were dissociated, sorption decreased considerably (up to a factor of 14), although the non-dissociated hormones testosterone and progesterone indicated greater sorption to humic acid at pH 10 compared to the partially deprotonated estradiol and estrone. This study demonstrates that SPME can be used to assess organic matter sorption behaviour of a selected range of micropollutants and at environmentally relevant organic matter concentrations.

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.

Effect of Pseudomonas and Bacillus bacteria on Yield and Nutrient Uptake in Comparison with Chemical and Organic Fertilizers in Wheat

Directory of Open Access Journals (Sweden)

A. Fallah Nosrat Abad

2015-06-01

Full Text Available The high cost of fertilizers in farming systems, soil pollution and degradation of soil are factors that caused to full use of available renewable nutrient sources of plant (organic and biological with optimal application of fertilizers in order to maintain fertility, structure, biological activity, exchange capacity and water-holding capacity of the water in soil. Therefore, in recent years, according to investigators biofertilizers and organic farming as an alternative to chemical fertilizers has been drawn. Through this study, we examined the effects of triple superphosphate, organic matters and phosphate solubilizing microorganisms on quantitative and qualitative yield of wheat and nutrient uptake. The experiment was carried out in the factorial based on randomized complete block design. The factors were: 1-phosphate solubilizing bacteria in three levels including control, Pseudomonas Putida and Bacillus Coagulans bacteria, 2- triple superphosphate in five levels of 0, 25%, 50%, 75% and 100% and 3-organic matter in 2 levels of 0 and 15 ton/ha in the soil with high phosphorous accessibility (13 mg/kg soil but lower than sufficient limit for plant 15 mg/kg soil. The results showed that the highest amount of yield has been recorded in Pseudomonas Putida bacteria treatment with organic matter and 25% phosphate fertilizer. As a result, at the conditions of this experiment phosphate solubilizing bacteria and organic matter significantly had higher yield than control and their combination with phosphate fertilizer had significant effect on reducing phosphate fertilizer use.

Dissolved organic matter in sea spray: a transfer study from marine surface water to aerosols

Science.gov (United States)

Schmitt-Kopplin, P.; Liger-Belair, G.; Koch, B. P.; Flerus, R.; Kattner, G.; Harir, M.; Kanawati, B.; Lucio, M.; Tziotis, D.; Hertkorn, N.; Gebefügi, I.

2012-04-01

Atmospheric aerosols impose direct and indirect effects on the climate system, for example, by absorption of radiation in relation to cloud droplets size, on chemical and organic composition and cloud dynamics. The first step in the formation of Organic primary aerosols, i.e. the transfer of dissolved organic matter from the marine surface into the atmosphere, was studied. We present a molecular level description of this phenomenon using the high resolution analytical tools of Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) and nuclear magnetic resonance spectroscopy (NMR). Our experiments confirm the chemoselective transfer of natural organic molecules, especially of aliphatic compounds from the surface water into the atmosphere via bubble bursting processes. Transfer from marine surface water to the atmosphere involves a chemical gradient governed by the physicochemical properties of the involved molecules when comparing elemental compositions and differentiating CHO, CHNO, CHOS and CHNOS bearing compounds. Typical chemical fingerprints of compounds enriched in the aerosol phase were CHO and CHOS molecular series, smaller molecules of higher aliphaticity and lower oxygen content, and typical surfactants. A non-targeted metabolomics analysis demonstrated that many of these molecules corresponded to homologous series of oxo-, hydroxy-, methoxy-, branched fatty acids and mono-, di- and tricarboxylic acids as well as monoterpenes and sugars. These surface active biomolecules were preferentially transferred from surface water into the atmosphere via bubble bursting processes to form a significant fraction of primary organic aerosols. This way of sea spray production leaves a selective biological signature of the surface water in the corresponding aerosol that may be transported into higher altitudes up to the lower atmosphere, thus contributing to the formation of secondary organic aerosol on a global scale or transported laterally with

Compositional changes of soil organic matter with cropping time were more profound in subsoils and distinct between Phaeozem and Chernozem in Northeast China

Science.gov (United States)

Soil organic matter (SOM) contributes to soil processes and is found both in shallow and deep soil layers. Its activity can be affected by its chemical composition, yet knowledge is incomplete of how land use alters the structural composition of SOM throughout the profiles of different soil types. T...

Organic Matter Decomposition following Harvesting and Site Preparation of a Forested Wetland

Science.gov (United States)

Carl C. Trettin; M. Davidian; M.F. Jurgensen; R. Lea

1996-01-01

Organic matter accumulation is an important process that affects ecosystem function in many northern wetlands. The cotton strip assay (CSA)was used to measure the effect of harvesting and two different site preparation treatments, bedding and trenching, on organic matter decomposition in a forested wetland. A Latin square experimental design was used to determine the...

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

Dynamics of organic matter and microbial populations in amended soil: a multidisciplinary approach

Science.gov (United States)

Gigliotti, Giovanni; Pezzolla, Daniela; Zadra, Claudia; Albertini, Emidio; Marconi, Gianpiero; Turchetti, Benedetta; Buzzini, Pietro

2013-04-01

The application of organic amendments to soils, such as pig slurry, sewage sludge and compost is considered a tool for improving soil fertility and enhancing C stock. The addition of these different organic materials allows a good supply of nutrients for plants but also contributes to C sequestration, affects the microbial activity and the transformation of soil organic matter (SOM). Moreover, the addition of organic amendment has gained importance as a source of greenhouse gas (GHG) emissions and then as a cause of the "Global Warming". Therefore, it is important to investigate the factors controlling the SOM mineralization in order to improve soil C sequestration and decreasing at the same time the GHG emissions. The quality of organic matter added to the soil will play an important role in these dynamics, affecting the microbial activity and the changes in microbial community structure. A laboratory, multidisciplinary experiment was carried out to test the effect of the amendment by anaerobic digested livestock-derived organic materials on labile organic matter evolution and on dynamics of microbial population, this latter both in terms of consistence of microbial biomass, as well as in terms of microbial biodiversity. Different approaches were used to study the microbial community structure: chemical (CO2 fluxes, WEOC, C-biomass, PLFA), microbiological (microbial enumeration) and molecular (DNA extraction and Roche 454, Next Generation Sequencing, NGS). The application of fresh digestate, derived from the anaerobic treatment of animal wastes, affected the short-term dynamics of microbial community, as reflected by the increase of CO2 emissions immediately after the amendment compared to the control soil. This is probably due to the addition of easily available C added with the digestate, demonstrating that this organic material was only partially stabilized by the anaerobic process. In fact, the digestate contained a high amounts of available C, which led to

Sorption, degradation and leaching of pesticides in soils amended with organic matter: A review

Directory of Open Access Journals (Sweden)

Fardin Sadegh-Zadeh

2017-04-01

Full Text Available The use of pesticides in modern agriculture is unavoidable because they are required to control weeds. Pesticides are poisonous; hence, they are dangerous if misused. Understanding the fate of pesticides will be useful to use them safely. Therefore, contaminations of water and soil resources could be avoided. The fates of pesticides in soils are influenced by their sorption, decomposition and movement. Degradation and leaching of pesticides are control by sorption. Soil organic matter and clay content are main soil constituents that have a high capacity for sorption of pesticides. Addition of organic maters to amend the soils is a usual practice that every year has been done in a huge area of worldwide.  The added organic amendments to the soils affect the fate of pesticides in soils as well. Pesticides fates in different soils are different. The addition of organic matter to soils causes different fates for pesticides as well. It is known from the studies that sorption of non-ionic pesticides by soil in aqueous system is controlled mainly by the organic matter content of the soils. Sorption of pesticides has been reported to increase by amending soils with organic matter. In general, conditions that promote microbial activity enhance the rate of pesticides degradation, and those that inhibit the growth of microorganisms reduce the rate of degradation. Amendment of soils with organic matter may modify leaching of pesticides in soil. Some studies showed that organic matter added to soils reduced pesticides in ground water. Generally, organic amendments induces the restriction of pesticides leaching in soils.

Organic and inorganic speciation of particulate matter formed during different combustion phases in an improved cookstove.

Science.gov (United States)

Leavey, Anna; Patel, Sameer; Martinez, Raul; Mitroo, Dhruv; Fortenberry, Claire; Walker, Michael; Williams, Brent; Biswas, Pratim

2017-10-01

Residential solid fuel combustion in cookstoves has established health impacts including bladder and lung cancers, cataracts, low birth weight, and pneumonia. The chemical composition of particulate matter (PM) from 4 commonly-used solid fuels (coal, dung, ambient/dry applewood, and oakwood pellets), emitted from a gasifier cookstove, as well as propane, were examined. Temporal changes between the different cookstove burn-phases were also explored. Normalized concentrations of non-refractory PM 1 , total organics, chloride, ammonium, nitrate, sulfate, and 41 particle-phase polycyclic aromatic hydrocarbons (PAHs) were measured using a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) and a Thermal desorption Aerosol Gas chromatograph (TAG), respectively. Coal demonstrated the highest fraction of organic matter in its particulate emission composition (98%), followed by dung (94%). Coal and dung also demonstrated the highest numbers and concentrations of PAHs. While dry applewood emitted ten times lower organic matter compared to ambient applewood, a higher fraction of these organics was composed of PAHs, especially the more toxic ones such as benzo(a)pyrene (9.63ng/L versus 0.04ng/L), and benzo(b)fluoranthene (31.32ng/L versus 0.19ng/L). Data from the AMS demonstrated no clear trends for any of the combustion fuels over the different combustion phases unlike the previously reported trends observed for the physical characteristics. Of the solid fuels, pellets demonstrated the lowest emissions. Emissions from propane were below the quantification limit of the instruments. This work highlights the benefits of incorporating additional metrics into the cookstove evaluation process, thus enriching the existing PM data inventory. Copyright © 2017. Published by Elsevier Inc.

Metal-organic frameworks for the removal of toxic industrial chemicals and chemical warfare agents.

Science.gov (United States)

Bobbitt, N Scott; Mendonca, Matthew L; Howarth, Ashlee J; Islamoglu, Timur; Hupp, Joseph T; Farha, Omar K; Snurr, Randall Q

2017-06-06

Owing to the vast diversity of linkers, nodes, and topologies, metal-organic frameworks can be tailored for specific tasks, such as chemical separations or catalysis. Accordingly, these materials have attracted significant interest for capture and/or detoxification of toxic industrial chemicals and chemical warfare agents. In this paper, we review recent experimental and computational work pertaining to the capture of several industrially-relevant toxic chemicals, including NH 3 , SO 2 , NO 2 , H 2 S, and some volatile organic compounds, with particular emphasis on the challenging issue of designing materials that selectively adsorb these chemicals in the presence of water. We also examine recent research on the capture and catalytic degradation of chemical warfare agents such as sarin and sulfur mustard using metal-organic frameworks.

PHYS: Division of Physical Chemistry 258 - Properties and Origins of Cometary and Asteroidal Organic Matter Delivered to the Early Earth

Science.gov (United States)

Messenger, Scott; Nguyen, Ann

2017-01-01

Comets and asteroids may have contributed much of the Earth's water and organic matter. The Earth accretes approximately 4x10(exp 7) Kg of dust and meteorites from these sources every year. The least altered meteorites contain complex assemblages of organic compounds and abundant hydrated minerals. These carbonaceous chondrite meteorites probably derive from asteroids that underwent hydrothermal processing within the first few million years after their accretion. Meteorite organics show isotopic and chemical signatures of low-T ion-molecule and grain-surface chemistry and photolysis of icy grains that occurred in cold molecular clouds and the outer protoplanetary disk. These signatures have been overprinted by aqueously mediated chemistry in asteroid parent bodies, forming amino acids and other prebiotic molecules. Comets are much richer in organic matter but it is less well characterized. Comet dust collected in the stratosphere shows larger H and N isotopic anomalies than most meteorites, suggesting better preservation of primordial organics. Rosetta studies of comet 67P coma dust find complex organic matter that may be related to the macromolecular material that dominates the organic inventory of primitive meteorites. The exogenous organic material accreting on Earth throughout its history is made up of thousands of molecular species formed in diverse processes ranging from circumstellar outflows to chemistry at near absolute zero in dark cloud cores and the formative environment within minor planets. NASA and JAXA are currently flying sample return missions to primitive, potentially organic-rich asteroids. The OSIRIS-REx and Hayabusa2 missions will map their target asteroids, Bennu and Ryugu, in detail and return regolith samples to Earth. Laboratory analyses of these pristine asteroid samples will provide unprecedented views of asteroidal organic matter relatively free of terrestrial contamination within well determined geological context. Studies of

Response of Arabica Coffee Cultivated on Andisols on Organic Matter Applications

Directory of Open Access Journals (Sweden)

Pujiyanto .

2013-12-01

Full Text Available Andisols  are characterized  by  dominance  of  amorphous  minerals  which form strong and stable bonding with organic matter, therefore Andisols always contain high organic matter. For that reason, organic fertilizer is generally not applied  on  Andisols,  because  it  is  assumed  that  it  will  not  give   any  positive effect  on  growth  or  yield.  The  experiment  was  aimed  to  evaluate  response  of mature Kartika 1  Arabica coffee variety (seven years old cultivated on  Andisols applied with organic matter derived from cow dung manure. The experiment was carried out at Andungsari  Experimental Station located in Bondowoso District, East  Java. Elevation of the site was 1,150 m asl., with rainfall type of C (Schmidt &  Fergusson.  The  experiment  was    arranged  according  to  completely randomized  block  design  with  four  replications  to  evaluate  effect  of  ninecombination  treatments  of  application  rates  at   application  depths  of  50,  100, and 150 cm. The  range of organic fertilizers rates were  0 - 13.5 kg/tree/year. The experiment revealed that cow dung manure applications on Arabica coffee cultivated  on  Andisols  significantly  increased  yield  at  the  average  of  33% compared  to  the  untreated  crop.  No  significant  effect  of  the  treatment  onvariables of leaf water deficit and soil moisture content during dry season and root  density.  At  range  of  application  depths  of  50  -  150  cm,  the  deeper  the organic matter applications, the higher the yield will be.Key words: Andisols, Arabica coffee, organic matter, cow dung manure

Soil Quality of Restinga Forest: Organic Matter and Aluminum Saturation

Science.gov (United States)

Rodrigues Almeida Filho, Jasse; Casagrande, José Carlos; Martins Bonilha, Rodolfo; Soares, Marcio Roberto; Silva, Luiz Gabriel; Colato, Alexandre

2013-04-01

The restinga vegetation (sand coastal plain vegetation) consists of a mosaic of plant communities, which are defined by the characteristics of the substrates, resulting from the type and age of the depositional processes. This mosaic complex of vegetation types comprises restinga forest in advanced (high restinga) and medium regeneration stages (low restinga), each with particular differentiating vegetation characteristics. Of all ecosystems of the Atlantic Forest, restinga is the most fragile and susceptible to anthropic disturbances. The purpose of this study was evaluating the organic matter and aluminum saturation effects on soil quality index (SQI). Two locations were studied: State Park of the Serra do Mar, Picinguaba, in the city of Ubatuba (23°20' e 23°22' S / 44°48' e 44°52' W), and State Park of Cardoso Island in the city of Cananéia (25°03'05" e 25°18'18" S / 47°53'48" e 48° 05'42" W). The soil samples were collect at a depth of 0-10 cm, where concentrate 70% of vegetation root system. Was studied an additive model to evaluate soil quality index. The shallow root system development occurs due to low calcium levels, whose disability limits their development, but also can reflect on delay, restriction or even in the failure of the development vegetation. The organic matter is kept in the soil restinga ecosystem by high acidity, which reduces the decomposition of soil organic matter, which is very poor in nutrients. The base saturation, less than 10, was low due to low amounts of Na, K, Ca and Mg, indicating low nutritional reserve into the soil, due to very high rainfall and sandy texture, resulting in high saturation values for aluminum. Considering the critical threshold to 3% organic matter and for aluminum saturation to 40%, the IQS ranged from 0.95 to 0.1 as increased aluminum saturation and decreased the soil organic matter, indicating the main limitation to the growth of plants in this type of soil, when deforested.

Municipal wastewater treatment for effective removal of organic matter and nitrogen

International Nuclear Information System (INIS)

Grebenevich, E.V.; Zaletova, N.A.; Terentieva, N.A.

1987-01-01

The organic matter, as well as nitrogen and phosphorus, are nutrient substances. Their excess concentrations in water receiving bodies lead to eutrophication, moreover, the nitrogen content in water bodies is standardized according the sanitary-toxicological criterion of harmfulness: NH 4 + -N ≤0,39-2,0 mgl - , NO 3 -N ≤9,1-10 mgl - . The municipal wastewater contain, usually, organic matter estimated by BOD 150-200 mgl - , and COD 300-400 mgl - , the nitrogen compounds 50-60 mgl - , and NH 4 + -N 20-25 mgl - . NO x -N are practically absent. Their presence indicated on discharge of industrial wastewater. The total phosphorus is present in the concentration of 15 mgl - , PO 4 - - P 5-8 mgl - . Activated sludge process has been most widely used in the USSR for municipal wastewater treatment. The activated sludge is biocenoses of heterotrophic and auto trophic microorganisms. They consume nutrient matters, transferring pollution of wastewater by means of enzyme systems in acceptable forms. C, N and P-containing matters are removed from wastewater by biological intake for cell synthesis. Moreover C- containing matters are removed by oxidation to CO 2 and H 2 O. P-containing compounds under definite conditions associate with solid fraction of activated sludge and thus simultaneously removed from wastewater. The removal of nitrogen in addition to biosynthesis is carried out only in the denitrification process, when oxygen of NO x -N is used for oxidation of organic matter and produced gaseous nitrogen escapes into the atmosphere

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)

Processes controlling the production of aromatic water-soluble organic matter during litter decomposition

NARCIS (Netherlands)

Klotzbücher, T.; Kaiser, K.; Filley, T.R.; Kalbitz, K.

2013-01-01

Dissolved organic matter (DOM) plays a fundamental role for many soil processes. For instance, production, transport, and retention of DOM control properties and long-term storage of organic matter in mineral soils. Production of water-soluble compounds during the decomposition of plant litter is a

Bulk Soil Organic Matter d2H as a Precipitation Proxy

Science.gov (United States)

Williams, E. K.; Terwilliger, V. J.; Nakamoto, B. J.; Berhe, A. A.; Fogel, M. L.

2016-12-01

The stable hydrogen isotopic composition (d2H) of leaf waxes have traditionally been used to infer modern and paleoclimate precipitation sources. However, the extent to which evapotranspiration of leaf waters affects the d2H of plant leaf waxes remains hotly contested with offsets varying between species. Because of the relative importance of root organic matter contribution to bulk soil pools compared to litter/leaves and the minimal fractionation between soil water and root material, it is plausible that bulk soil organic matter d2H may be an option for modern and paleoclimate precipitation reconstructions. In this study, we analyzed the non-exchangeable d2H composition of roots, litter, leaves, and bulk soils along an elevation gradient in the southern Sierra Nevada range (USA). Our results show a consistent offset of 30 ± 3‰ in bulk soil organic matter in surface soils from the measured precipitation. This consistent relationship with precipitation was not found in any of the other organic materials that we measured and implies that d2H bulk soil organic matter can record precipitation signals regardless of above-ground species composition. Additionally, we utilized physical density fractionation to determine which fractions (which vary in level of mineral association and in turnover time) of the soil control this relationship. These findings and how this relationship holds with depth will be presented in conjunction with data from a soil profile on the Ethiopian plateau spanning 6000 years.

Elimination kinetic model for organic chemicals in earthworms.

NARCIS (Netherlands)

Dimitrova, N.; Dimitrov, S.; Georgieva, D.; van Gestel, C.A.M.; Hankard, P.; Spurgeon, D.J.; Li, H.; Mekenyan, O.

2010-01-01

Mechanistic understanding of bioaccumulation in different organisms and environments should take into account the influence of organism and chemical depending factors on the uptake and elimination kinetics of chemicals. Lipophilicity, metabolism, sorption (bioavailability) and biodegradation of

Metal Speciation in Landfill Leachates with a Focus on the Influence of Organic Matter

Energy Technology Data Exchange (ETDEWEB)

F Claret; C Tournassat; C Crouzet; E Gaucher; T Schäfer; G Braibant; D Guyonnet

2011-12-31

This study characterizes the heavy-metal content in leachates collected from eight landfills in France. In order to identify heavy metal occurrence in the different size fractions of leachates, a cascade filtration protocol was applied directly in the field, under a nitrogen gas atmosphere to avoid metal oxidation. The results of analyses performed on the leachates suggest that most of the metals are concentrated in the <30 kDa fraction, while lead, copper and cadmium show an association with larger particles. Initial speciation calculations, without considering metal association with organic matter, suggest that leachate concentrations in lead, copper, nickel and zinc are super-saturated with respect to sulphur phases. Speciation calculations that account for metal complexation with organic matter, considered as fulvic acids based on C1(s) NEXAFS spectroscopy, show that this mechanism is not sufficient to explain such deviation from equilibrium conditions. It is therefore hypothesized that the deviation results also from the influence of biological activity on the kinetics of mineral phase precipitation and dissolution, thus providing a dynamic system. The results of chemical analyses of sampled fluids are compared with speciation calculations and some implications for the assessment of metal mobility and natural attenuation in a context of landfill risk assessment are discussed.

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

Non-pharmacological modulation of cerebral white matter organization

DEFF Research Database (Denmark)

Kristensen, Tina D; Mandl, Rene C W; Jepsen, Jens R M

2018-01-01

OBJECTIVE: Neuroplasticity is a well-described phenomenon, but effects of non-pharmacological interventions on white matter (WM) are unclear. Here we review associations between active non-pharmacological interventions and WM organization in healthy subjects and in psychiatric patients. METHOD...

Distribution of some organic components in two forest soils profiles with evidence of soil organic matter leaching.

Science.gov (United States)

Álvarez-Romero, Marta; Papa, Stefania; Lozano-García, Beatriz; Parras-Alcántara, Luis; Coppola, Elio

2015-04-01

Soil stores organic carbon more often than we can find in living vegetation and atmosphere together. This reservoir is not inert, but it is constantly in a dynamic phase of inputs and losses. Soil organic carbon mainly depends on land cover, environment conditions and soil properties. After soil deposition, the organic residues of different origin and nature, the Soil Organic Matter (SOM) can be seen involved in two different processes during the pedogenesis: mineralization and humification. The transport process along profile happens under certain conditions such as deposition of high organic residues amount on the top soil, high porosity of the soil caused by sand or skeleton particles, that determine a water strong infiltrating capacity, also, extreme temperatures can slow or stop the mineralization and/or humification process in one intermediate step of the degradation process releasing organic metabolites with high or medium solubility and high loads of water percolating in relation to intense rainfall. The transport process along soil profile can take many forms that can end in the formation of Bh horizons (h means accumulation of SOM in depth). The forest cover nature influence to the quantity and quality of the organic materials deposited with marked differences between coniferous and deciduous especially in relation to resistance to degradation. Two soils in the Campania region, located in Lago Laceno (Avellino - Italy) with different forest cover (Pinus sp. and Fagus sp.) and that meets the requirements of the place and pedological formation suitable for the formation and accumulation of SOM in depth (Bh horizon) were studied. The different soil C fractions were determinated and were assessed (Ciavatta C. et al. 1990; Dell'Abate M.T. et al. 2002) for each soil profile the Total Extractable Lipids (TEL). Furthermore, the lignin were considered as a major component of soil organic matter (SOM), influencing its pool-size and its turnover, due to the high

Note on the chemical potential of decoupled matter in the Universe

NARCIS (Netherlands)

Nieuwenhuizen, T.M.; Pombo, C.

2011-01-01

Textbooks on cosmology exhibit a thermodynamic inconsistency for free streaming, decoupled matter. It is connected here to the chemical potential, which deviates from its equilibrium value μ = @kBT , where @ is the usual parameter of the Fermi-Dirac or Bose-Einstein distribution function.

Organic matter characterization during the anaerobic digestion of different biomasses by means of CPMAS 13C NMR spectroscopy

International Nuclear Information System (INIS)

Tambone, Fulvia; Adani, Fabrizio; Gigliotti, Giovanni; Volpe, Daniela; Fabbri, Claudio; Provenzano, Maria Rosaria

2013-01-01

The aim of this work was to characterize ingestates and their corresponding digestates obtained in two full-scale biogas production plants processing a) mixtures of organic wastes in co-digestion, and b) pig slurry in order to assess the organic matter transformation during anaerobic digestion by means of chemical analysis and 13 CPMAS-NMR spectroscopy. Results proved that digestates obtained by different organic substrates exhibited significant chemical differences related to the different initial composition of substrates. We proposed the use of the aliphaticity index in order to highlight the different chemical nature of ingestates and their corresponding digestates. In order to verify whether the AD process leads to stabilized final products regardless the initial composition of biomass in view of a possible agronomical use of digestate, a comparison of CPMAS 13 C NMR data of a number of ingestates and digestates available in literature was carried out. Results indicated that most of the aromatic structures present in the substrate tend to degrade during the process and that anaerobic digestion proceeds through preferential degradation of carbohydrates such as cellulose and hemicellulose and, as a consequence, concentration of more chemically recalcitrant aliphatic molecules occurs. -- Highlights: ► We studied anaerobic digestion by means of chemical analysis and 13 CPMAS-NMR spectroscopy. ► Significant chemical differences in digestates were highlighted. ► We proposed the use of the aliphaticity index in order to differentiate digestates. ► Most of the aromatic structures tend to degrade. ► Carbohydrates are degraded and recalcitrant aliphatic molecules concentrate

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...

Soil organic matter stabilization in buried paleosols of the Great Plains

Science.gov (United States)

Chaopricha, N. T.; Marin-Spiotta, E.; Mason, J. A.; Mueller, C. W.

2010-12-01

Understanding the mechanisms that control soil organic matter (SOM) stabilization is important for understanding how soil carbon is sequestered over millennia, and for predicting how future disturbances may affect soil carbon stocks. We are studying the mechanisms controlling SOM stabilization in the Brady Soil, a buried paleosol in Holocene loess deposits spanning much of the central Great Plains of the United States. The Brady Soil developed 9,000-13,500 years ago during a time of warming and drying that resulted in a shift from C3 to C4 dominated plants. The Brady soil is unusual in that it has very dark coloring, although it contains less than separate particulate organic matter associated with minerals from that within and outside of soil aggregates. We found the largest and darkest amounts of organic C in aggregate-protected SOM greater than 20 µm in diameter. Density and textural fractionation revealed that much of the SOM is bound within aggregates, indicating that protection within aggregates is a major contributor to SOM- stabilization in the Brady Soil. We are conducting a long-term lab soil incubation with soils collected from the modern A horizon and the Brady Soil to determine if the buried SOM becomes microbially available when exposed to the modern atmosphere. We are measuring potential rates of respiration and production of CH4 and N2O. Results so far show respiration rates at field moisture for both modern and buried horizons are limited by water, suggesting dry environmental conditions may have helped to preserve SOM in the Brady Soil. We are investigating the potential for chemical stabilization of the dark SOM preserved in the buried paleosol by characterizing C chemistry using solid-state 13C-NMR spectroscopy. Furthermore, we plan to use lipid analyses and pyrolysis GC/MS to determine likely sources for the SOM: microbial vs plant. Combining information on the physical location of SOM in the soil, its chemical composition, decomposability

Sorption of organic chemicals at biogeochemical interfaces - calorimetric measurements

Science.gov (United States)

Krüger, J.; Lang, F.; Siemens, J.; Kaupenjohann, M.

2009-04-01

Biogeochemical interfaces in soil act as sorbents for organic chemicals, thereby controlling the degradation and mobility of these substances in terrestrial environments. Physicochemical properties of the organic chemicals and the sorbent determine sorptive interactions. We hypothesize that the sorption of hydrophobic organic chemicals ("R-determined" chemicals) is an entropy-driven partitioning process between the bulk aqueous phase and biogeochemical interface and that the attachment of more polar organic chemicals ("F-determined" chemicals) to mineral surfaces is due to electrostatic interactions and ligand exchange involving functional groups. In order to determine thermodynamic parameters of sorbate/sorbent interactions calorimetric titration experiments have been conducted at 20˚ C using a Nanocalorimeter (TAM III, Thermometric). Solutions of different organic substances ("R-determined" chemicals: phenanthrene, bisphenol A, "F-determined" chemicals: MCPA, bentazone) with concentrations of 100 mol l-1 were added to suspensions of pure minerals (goethite, muscovite, and kaolinite and to polygalacturonic acid (PGA) as model substance for biofilms in soil. Specific surface, porosity, N and C content, particle size and point of zero charge of the mineral were analyzed to characterize the sorbents. The obtained heat quantities for the initial injection of the organic chemicals to the goethite were 55 and 71 J for bisphenol A and phenanthrene ("R-determined representatives") and 92 and 105 J for MCPA and bentazone ("F-determined" representatives). Further experiments with muscovite, kaolinite and PGA are in progress to determine G and H of the adsorption process.

Differential recycling of coral and algal dissolved organic matter via the sponge loop

NARCIS (Netherlands)

Rix, L.; de Goeij, J.M.; van Oevelen, D.; Struck, U.; Al-Horani, F.A.; Wild, C.; Naumann, M.S.

Corals and macroalgae release large quantities of dissolved organic matter (DOM), one of the largest sources of organic matter produced on coral reefs. By rapidly taking up DOM and transforming it into particulate detritus, coral reef sponges are proposed to play a key role in transferring the

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...

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

International Nuclear Information System (INIS)

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

2016-01-01

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

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...

Effect of chemically processed bonemeal alone and in combination with organic materials on plant growth. [Part] I : Rice-wheat rotation in an alluvial soil

International Nuclear Information System (INIS)

Ramasami, S.; Vimal, O.P.

1975-01-01

The effect of chemically processed bonemeal added 60 kg P 2 O /ha alone and in combination with various organic materials viz., wheat straw and rice straw 3 tons/hs, starch 500 kg/ha and EDTA 250 kg/ha was studied on rice in an alluvial soil. The residual effect was studied on wheat using 32 P as a tracer. The results showed that in the first crop(rice) bonemeal organic matter combination had a significant effect both on dry matter yield and nutrient uptake. In the second crop (wheat) except chemically processed honemeal in combination with EDTA, all other combinations showed a marked positive effect on yield, total P-uptake and 'A' values. Comparison of P-uptake from soil and fertilizer indicated that there was a marked residual effect on the subsequent wheat crop. (author)

Organic Matter Quality and Partitioning of Polychlorinated Biphenyls

National Research Council Canada - National Science Library

Brannon, James

1997-01-01

...). Equilibrium partitioning of neutral organic chemicals between the organic carbon fraction of bedded sediments and the interstitial water of the sediments provides the theoretical basis for the most...

Air oxidation of samples from different clay formations of East Paris basin: quantitative and qualitative consequences on the dissolved organic matter

International Nuclear Information System (INIS)

Blanchart, Pascale; Faure, Pierre; Michels, Raymond; Parant, Stephane

2012-01-01

Document available in extended abstract form only. During the excavation and the building of an underground research laboratory in clay geological formations, exposure to air is one of the most important parameters affecting the composition of fossil organic matter. Indeed the net effect of air oxidation of the organic matter is enrichment in oxygen and carbon combined with a loss of hydrogen. Effluents formed are CO 2 and water as well as the liberation of hydrocarbons. This process may have an impact on water chemistry of the clay, especially on the quantity and composition of Dissolved Organic Matter (DOM). The clays studied were the following and may be distinguished on the basis of their organic matter content: - The Callovo-Oxfordian argillite, collected in the Bure Underground Research Laboratory (Meuse, France), which contains a mixture of type II and III kerogen; - The Toarcian shales of East Paris Basin collected from drilling EST 204 (Meuse, France) contains type II kerogen; - The Kimmeridgian shales of East Paris Basin collected from drilling HTM 102 (Meuse, France) also contains type II kerogen. The powdered clay samples were oxidized in a ventilated oven at 100 C under air flow during 2, 256, 512 and 1088 hours for Callovo-Oxfordian samples and during 512 and 2048 hours for Toarcian and Kimmeridgian samples. The DOM of each sample was extracted by soxhlet using pure water. Different analyses were carried out: - Quantitative evolution of DOM with the oxidation process; - Evolution of several chemical parameters of DOM with oxidation using molecular analyses (PyGC-MS) molecular weight distribution (GPC-HPLC) as well as spectroscopic measurements (3D-Fluorescence). Increasing oxidation induces an increase of DOC values for all samples. Also, Changes in the chemical composition of the DOM are observed: decrease in the molecular weight range; enrichment in acidic functional groups (alkane-dioic acids, alkanoic acids, aromatics poly acids). Moreover the