Organic Carbon Content (organic + carbon_content)

Distribution by Scientific Domains

Kinds of Organic Carbon Content

  • total organic carbon content


  • Selected Abstracts


    Determination of Total Organic Carbon Content and ,13C in Carbonate-Rich Detrital Sediments

    GEOSTANDARDS & GEOANALYTICAL RESEARCH, Issue 3 2007
    Valier Galy
    carbone organique; décarbonatation; solubilisation; sediment; carbonate The determination of total organic carbon content and composition in detrital sediments requires careful removal of their carbonate minerals. In detrital sediments containing large amounts of carbonates, including dolomite, this can only be achieved by liquid acid leaching that may solubilise a significant proportion of the organic carbon. For a set of detrital sediments from the Himalayan system and the Amazon River as well as five geological reference materials, we determined the proportion of organic carbon (Corg) solubilised during acid leaching. This proportion is significant for all analysed sediments and generally tends to increase with the organic carbon content. Compared to other types of sediments analysed, clay fractions extracted from river sediments and bed sediments with very low organic carbon content have high and low proportions of acid soluble Corg respectively. In Himalayan and Amazon river sediments, the proportion of Corg solubilised during acid leaching was relatively constant with average values of 14 and 19 % respectively. Thus, it is possible to correct the Corg content for the dissolved organic carbon content measured after decarbonation. Data presented here show that Corg dissolved during liquid acid leaching must be taken into account. After careful calibration, the method presented here should, therefore, be applied to any carbonate-rich detrital sediment. La détermination de la teneur totale en carbone organique et de sa composition dans des sédiments détritiques requiert leur décarbonatation préalable. l'élimination complète de carbonates tels que la dolomite ne peut être réalisée qu'au moyen d'une attaque avec un acide en phase liquide ce qui peut entrainer la solubilisation d'une partie du carbone organique. Pour un ensemble de sédiments détritiques provenant du système Himalayen et de l'Amazone ainsi que pour cinq matériaux géologiques de référence, nous avons déterminé la proportion de carbone organique (Corg) solubilisé lors de la décarbonatation. Celle-ci est significative pour l'ensemble des sédiments analysés et tend à augmenter avec la teneur en carbone organique. En comparaison avec les autres types de sédiments analysés, les fractions argileuses extraites de sédiments de rivière et les sédiments de fond très pauvres en Corg ont une proportion de Corg soluble dans l'acide respectivement élevée et faible. Dans les sédiments himalayens et amazoniens, la proportion de Corg solubilisé lors de la décarbonatation est plutôt constante avec des valeurs moyennes respectives de 14 et 19%. Nous pouvons donc calculer avec précision la teneur totale en carbone organique à partir de la teneur en Corg déterminée après décarbonatation. Nos données montrent que la solubilisation de Corg lors de la décarbonatation par un acide en solution est importante et doit être prise en compte lors de la détermination de la teneur en carbone organique. Moyennant une calibration minutieuse, la méthode que nous présentons devrait donc être utilisée pour l'analyse de sédiments détritiques riches en carbonates. [source]


    Rainwater Dissolved Organic Carbon: Characterization of Surface Active Substances by Electrochemical Method

    ELECTROANALYSIS, Issue 19-20 2007
    osovi
    Abstract Surface active substances as organic constituents of bulk precipitation were studied by AC voltammetric method. Adsorption characteristics at the mercury electrode of real rainwater samples are compared with aqueous solutions of a number model substances suggested to be representative of water soluble organic compounds (WSOC) in atmospheric aerosols and droplets: monocarboxylic, dicarboxylic, and polyacidic compounds, levoglucosan, polyaromatic hydrocarbon naphtalene and anionic surfactant sodium dodecylbenzene sulfonate. On the basis of the capacitance vs. potential curves and the surfactant activity normalized to the organic carbon content it is concluded that humic like substances, monocarboxylic acids and polyaromatic hydrocarbons may play an important role in atmospheric aquatic system because of their surface active potential. [source]


    Molecular diversity and characterization of nitrite reductase gene fragments (nirK and nirS) from nitrate- and uranium-contaminated groundwater

    ENVIRONMENTAL MICROBIOLOGY, Issue 1 2003
    Tingfen Yan
    Summary Nitrate-contaminated groundwater samples were analysed for nirK and nirS gene diversity. The samples differed with respect to nitrate, uranium, heavy metals, organic carbon content, pH and dissolved oxygen levels. A total of 958 nirK and 1162 nirS clones were screened by restriction fragment length polymorphism (RFLP) analysis: 48 and 143 distinct nirK and nirS clones, respectively, were obtained. A single dominant nirK restriction pattern was observed for all six samples and was 83% identical to the Hyphomicrobium zavarzinii nirK gene. A dominant nirS pattern was observed for four of the samples, including the background sample, and was 95% identical to the nirS of Alcaligenes faecalis. Diversity indices for nirK and nirS sequences were not related to any single geochemical characteristic, but results suggested that the diversity of nirK genes was inversely proportional to the diversity of nirS. Principal component analysis (PCA) of the sites based on geochemistry grouped the samples by low, moderate and high nitrate but PCA of the unique operational taxonomic units (OTUs) distributions grouped the samples differently. Many of the sequences were not closely related to previously observed genes and some phylogenetically related sequences were obtained from similar samples. The results indicated that the contaminated groundwater contained novel nirK and nirS sequences, functional diversity of both genes changed in relation to the contaminant gradient, but the nirK and nirS functional diversity was affected differently. [source]


    Effect of organic carbon content, clay type, and aging on the oral bioavailability of hexachlorobenzene in rats,

    ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 11 2007
    Shakil A. Saghir
    Abstract Bioavailability of lipophilic chemicals is influenced by the physicochemical properties of soils/sediment such as particle size, pH, clay, and organic carbon content. The present study investigated the effects of sediment composition and aging on the oral bioavailability of hexachlorobenzene (HCB) in rats. Formulated sediments were prepared using various ratios of kaolinite and montmorillonite clay, sand, peat moss, and black carbon, spiked with 14C-HCB, and orally administered to rats prior to and after one year of aging in dark at 10°C. In the nonaged sediments there was a 21 to 45% reduction in the oral bioavailability of HCB when compared to the corn oil standard without any clear pattern of the impact of the sediment clay and/or organic carbon content. One year of aging resulted in statistically significant (p = 0.049) reduction in the oral bioavailability of HCB from the sediments compared to the corn oil standard and nonaged sediment indicating stronger interactions between HCB and sediment contents with aging. The mean reduction in oral bioavailability after one year of aging ranged from approximately 5 to 14% greater than that observed for nonaged sediments. The fecal elimination of the HCB-derived radioactivity from the one-year-aged sediments was much higher than the nonaged sediments, consistent with the lower absorption from the gastrointestinal tract due to lower desorption of HCB from the aged sediments. Increase in the fecal elimination and decrease in oral bioavailability of 14C-HCB was related to the increase in clay and black carbon. [source]


    The long-term fate of polychlorinated biphenyls in San Francisco Bay (USA)

    ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 10 2004
    Jay A. Davis
    Abstract A simple one-box mass budget model is presented as a first step toward a quantitative understanding of the long-term fate of polychlorinated biphenyls (PCBs) in San Francisco Bay (USA). Sensitivity analysis indicated that the most influential input parameters were degradation half-life in sediment, Kow, outflow, average PCB concentration in sediment, and depth of the active sediment layer. Moderately influential parameters included organic carbon content of suspended solids, sediment burial mass transfer coefficient, and Henry's law constant. If external loading could be eliminated entirely, the mass of PCBs in the bay is predicted to drop to half of the present value in 20 years. The model predicts that sustained loading of 10 kg year,1 would prevent the total PCB mass in the bay from ever dropping below 10% of the present mass. With a sustained loading of 20 kg year,1, the model predicts that the total PCB mass would never fall below about 25% of the present mass. The half-lives in the bay for the individual PCB congeners evaluated in this report ranged from four years for PCB 18 to 30 years for PCB 194. [source]


    The potential for estradiol and ethinylestradiol to sorb to suspended and bed sediments in some English rivers

    ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 12 2002
    Karlijn I. E. Holthaus
    Abstract The endocrine-disrupting impact of steroid estrogens on fish will be strongly influenced by their distribution between sediment and water. Laboratory studies were performed to investigate the potential for sorption of 17,-estradiol (E2) and 17,-ethinylestradiol (EE2) to bed and suspended sediments taken from five British rivers. Sediment material was collected from the Rivers Aire and Calder (located in urban and industrialized areas in Yorkshire, UK), the River Thames (at a relatively rural site in Oxfordshire, UK), and from the estuaries of the Rivers Tees and Tyne. Using anaerobic conditions to inhibit biodegradation, it was found that 80 to 90% of binding to bed sediments was complete within 1 d, but that an equilibrium had not been reached after 2 d. Bed sediments gave distribution coefficients (Kd) ranging from 4 to 74 L/kg for E2 and from 8 to 121 L/kg for EE2 for samples taken over a range of seasons and locations. Sorption to suspended sediment gave Kd values ranging from 21 to 122 L/kg for E2 and 19 to 260 L/kg for EE2. However, these Kd values suggest less than 1% removal of the steroid estrogens from the aqueous phase given the ambient suspended sediment concentration. In the bed sediments, higher Kd values were associated with smaller particle size and higher organic carbon content. In most cases, the Kd values obtained for EE2 were higher than those for E2 by a factor of up to three. [source]


    Mutagenicity and disinfection by-products in surface drinking water disinfected with peracetic acid

    ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 2 2002
    Silvano Monarca
    Abstract The aims of this research were to study the influence of peracetic acid (PAA) on the formation of mutagens in surface waters used for human consumption and to assess its potential application for the disinfection of drinking water. The results obtained using PAA were compared to those found with sodium hypochlorite (NaClO) and chlorine dioxide (ClO2). The Ames test, root anaphase aberration assay, and root/micronuclei assay in Allium cepa and Tradescantia/micronuclei test were used to evaluate the mutagenicity of disinfected samples. Microbiological tests were also performed, and disinfection by-products (DBPs) were identified using gas chromatography/mass spectrometry (GC/MS). A slight bacterial mutagenicity was found in raw lake and river water, and similar activity was detected in disinfected samples. A plant test revealed genotoxicity in raw river water, and microbiological analysis showed that PAA has bactericidal activity but lower than that of the other disinfectants. The DBPs produced by PAA were mainly carboxylic acids, which are not recognized as mutagenic, whereas the waters treated with the other disinfectants showed the presence of mutagenic/carcinogenic halogenated DBPs. However, additional experiments should be performed with higher concentrations of PAA and using water with higher organic carbon content to better evaluate this disinfectant. [source]


    Chlorinated hydrocarbons in flatfishes from the Southern California, USA, Bight

    ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 6 2000
    Kenneth Schiff
    Abstract Alhough inputs of chlorinated hydrocarbon compounds to the Southern California Bight (SCB) are presently low, historical deposits represent a source of bioaccumulation potential to sediment-associated fauna. To assess this bioaccumulation potential, 14 chlorinated hydrocarbon classes were measured in livers of three species of flatfish collected from 63 randomly selected sites on the coastal shelf between Point Conception and the United States,Mexico international border. Tissue contamination was widespread throughout the SCB, but was limited to just two chlorinated hydrocarbon classes. Virtually 100% of Pacific sanddab (Citharichthys sordidus) and longfin sanddab (Citharichthys xanthostigma) populations were estimated to be contaminated with dichlorodiphenyltrichloroethane (total DDT = sum of o,p, and p,p, isomers of DDT + dichlorodiphenyldichloroethylene [DDE] + dichlorodiphenyldichloroethane [DDD]) and/or polychlorinated biphenyls (total PCBs). Total DDT also contaminated the majority (64%) of the Dover sole (Microstomus pacificus) population in the SCB. Total PCB measurements in tissues of SCB flatfish were dominated by 12 congeners (52, 66, 87, 101, 105, 118, 128, 138, 153, 170, 180, and 187), which averaged 95% of the combined mass of the 27 congeners analyzed. Sediment concentrations (normalized by total organic carbon content) accounted for most of the variability observed in tissue concentrations (normalized by lipid content) for 8 of these 12 congeners and total PCBs. Normalized sediment concentrations were also significantly correlated to normalized tissue concentrations for total DDT and p,p,-DDE. Tissue concentrations measured in this study from reference areas of the SCB were compared to tissue concentrations measured from reference areas in studies conducted in 1977 and 1985. Total DDT and total PCB liver concentrations were found to have decreased one to two orders of magnitude in Pacific and longfin sanddabs between 1985 and 1994. Total DDT and total PCB liver concentrations decreased 5- to 35-fold in Dover sole between 1977 and 1994. [source]


    Changes in shrinkage of restored soil caused by compaction beneath heavy agricultural machinery

    EUROPEAN JOURNAL OF SOIL SCIENCE, Issue 4 2008
    B. Schäffer
    Summary Compaction is a major cause of soil degradation. It affects not only the porosity of the soil, but also the soil's hydrostructural stability. Soil that is restored after temporary removal is particularly sensitive to compaction. We investigated the effects of trafficking with a heavy combine harvester on the shrinkage behaviour of a restored soil that had been gently cultivated for several years. We tested the hypothesis that compaction decreases the hydrostructural stability of restored soil by analysing simultaneously measured shrinkage and water retention curves of undisturbed soil samples. Shrinkage strongly depended on clay and organic carbon content. Taking account of this influence and normalizing the shrinkage parameters with respect to these soil properties, we found pronounced effects of trafficking on shrinkage. Ten passes with the combine harvester decreased the structural porosity by about 40% at maximum swelling and by about 30% at the shrinkage limit and increased the bulk density by 8% at maximum swelling and by 10% at the shrinkage limit, but did not significantly affect the porosity of the soil plasma. Moreover, trafficking modified shrinkage, increasing the slopes of the shrinkage curve in the basic and structural shrinkage domains by about 30% and more than 150% after 10 passes, respectively. Evidently the aggregate structure was strongly destabilized. The results indicate that the hydrostructural stability of the soil was still very sensitive to compaction by trafficking even 5 years after restoration. The analysis of shrinkage seemed well suited for the assessment of compaction effects on soil structure. [source]


    Temporal denitrification patterns in different horizons of two riparian soils

    EUROPEAN JOURNAL OF SOIL SCIENCE, Issue 1 2003
    A-C. Cosandey
    Summary The dynamics of biological denitrification in riparian soil is still poorly understood. We studied the spring-time pattern of denitrifying enzyme activity (DEA) and the rate of denitrification (DNT) in two hydromorphic riparian soils, one a mollic Gleysol and the other a terric Histosol. The average DEA ranged from 73 to 1232 ng N g,1 hour,1, and DNT ranged from 4 to 36 ng N g,1 hour,1. Both DEA and DNT diminished with increasing depth in both soil types. This decrease corresponded to a decrease in total and K2SO4 -extractable organic carbon and K2SO4 -extractable mineral nitrogen. The DEA and DNT differed in their dynamics. The former had no evident pattern in subsurface horizons but increased with temperature at the end of spring in surface and structural horizons. The DNT diminished as the soil dried in the mollic Gleysol when the water table fell. In the terric Histosol, the water table was still too high at the end of spring to affect the DNT. The results suggest that the vertical pattern of denitrification is related to that of organic carbon content. This organic carbon content determines biological activity and the supply of carbon and nitrous oxides. In biologically active horizons temperature drives the dynamics of DEA, whereas soil moisture drives the dynamics of DNT. Our results show the importance of the dynamic soil,water relationship in controlling denitrification within the riparian zone. [source]


    Soil solution concentration of Cd and Zn canbe predicted with a CaCl2 soil extract

    EUROPEAN JOURNAL OF SOIL SCIENCE, Issue 1 2003
    F. Degryse
    Summary Risk assessment of heavy metals in soil requires an estimate of the concentrations in the soil solution. In spite of the numerous studies on the distribution of Cd and Zn in soil, few measurements of the distribution coefficient in situ, Kd, have been reported. We determined the Kd of soils contaminated with Cd and Zn by measuring metal concentrations in the soil and in the soil solution and attempted to predict them from other soil variables by regression. Soil pH explained most of the variation in logKd (R2 = 0.55 for Cd and 0.70 for Zn). Introducing organic carbon content or cation exchange capacity (CEC) as second explanatory variable improved the prediction (R2 = 0.67 for Cd and 0.72 for Zn), but these regression models, however, left more than a factor of 10 of uncertainty in the predicted Kd. This large degree of uncertainty may partly be due to the variable degree of metal fixation in contaminated soils. The labile metal content was measured by isotopic dilution (E value). The E value ranged from 18 to 92% of the total metal content for Cd and from 5 to 68% for Zn. The prediction of Kd improved when metals in solution were assumed to be in equilibrium with the labile metal pool instead of the total metal pool. It seems necessary therefore to discriminate between ,labile' and ,fixed' pools to predict Kd for Cd and Zn in field contaminated soils accurately. Dilute salt extracts (e.g. 0.01 m CaCl2) can mimic soil solution and are unlikely to extract metals from the fixed pool. Concentrations of Cd and Zn in the soil solution were predicted from the concentrations of Cd and Zn in a 0.01 m CaCl2 extract. These predictions were better correlated with the observations for field contaminated soils than the predictions based on the regression equations relating logKd to soil properties (pH, CEC and organic C). [source]


    Essential fatty acids and phosphorus in seston from lakes with contrasting terrestrial dissolved organic carbon content

    FRESHWATER BIOLOGY, Issue 1 2007
    KELLY GUTSEIT
    Summary 1. It is often assumed that lakes highly influenced by terrestrial organic matter (TOM) have low zooplankton food quality because of elemental and/or biochemical deficiencies of the major particulate organic carbon pools. We used the biochemical [polyunsaturated fatty acids, especially eicosapentaenoic acid (EPA) , 20:5,3] and elemental (C : P ratio) composition of particulate matter (PM) as qualitative measures of potential zooplankton food in two categories of lakes of similar primary productivity, but with contrasting TOM influence (clear water versus humic lakes). 2. C : P ratios (atomic ratio) in PM were similar between lake categories and were above 400. The concentration (,g L,1) and relative content (,g mg C,1) of EPA, as well as the particulate organic carbon concentration, were higher in the humic lakes than in the clear-water lakes. 3. Our results show high fatty acid quality of PM in the humic lakes. The differences in the biochemical quality of the potential zooplankton food between lake categories can be attributed to the differences in their phytoplankton communities. 4. High biochemical quality of the food can result in high efficiency of energy transfer in the food chain and stimulate production at higher trophic levels, assuming that zooplankton are able to ingest and digest the resource available. [source]


    Overpressure and petroleum generation and accumulation in the Dongying Depression of the Bohaiwan Basin, China

    GEOFLUIDS (ELECTRONIC), Issue 4 2001
    X. Xie
    Abstract The occurrence of abnormally high formation pressures in the Dongying Depression of the Bohaiwan Basin, a prolific oil-producing province in China, is controlled by rapid sedimentation and the distribution of centres of active petroleum generation. Abnormally high pressures, demonstrated by drill stem test (DST) and well log data, occur in the third and fourth members (Es3 and Es4) of the Eocene Shahejie Formation. Pressure gradients in these members commonly fall in the range 0.012,0.016 MPa m,1, although gradients as high as 0.018 MPa m,1 have been encountered. The zone of strongest overpressuring coincides with the areas in the central basin where the principal lacustrine source rocks, which comprise types I and II kerogen and have a high organic carbon content (>2%, ranging to 7.3%), are actively generating petroleum at the present day. The magnitude of overpressuring is related not only to the burial depth of the source rocks, but to the types of kerogen they contain. In the central basin, the pressure gradient within submember Es32, which contains predominantly type II kerogen, falls in the range 0.013,0.014 MPa m,1. Larger gradients of 0.014,0.016 MPa m,1 occur in submember Es33 and member Es4, which contain mixed type I and II kerogen. Numerical modelling indicates that, although overpressures are influenced by hydrocarbon generation, the primary control on overpressure in the basin comes from the effects of sediment compaction disequilibrium. A large number of oil pools have been discovered in the domes and faulted anticlines of the normally pressured strata overlying the overpressured sediments; the results of this study suggest that isolated sandstone reservoirs within the overpressured zone itself offer significant hydrocarbon potential. [source]


    Determination of Total Organic Carbon Content and ,13C in Carbonate-Rich Detrital Sediments

    GEOSTANDARDS & GEOANALYTICAL RESEARCH, Issue 3 2007
    Valier Galy
    carbone organique; décarbonatation; solubilisation; sediment; carbonate The determination of total organic carbon content and composition in detrital sediments requires careful removal of their carbonate minerals. In detrital sediments containing large amounts of carbonates, including dolomite, this can only be achieved by liquid acid leaching that may solubilise a significant proportion of the organic carbon. For a set of detrital sediments from the Himalayan system and the Amazon River as well as five geological reference materials, we determined the proportion of organic carbon (Corg) solubilised during acid leaching. This proportion is significant for all analysed sediments and generally tends to increase with the organic carbon content. Compared to other types of sediments analysed, clay fractions extracted from river sediments and bed sediments with very low organic carbon content have high and low proportions of acid soluble Corg respectively. In Himalayan and Amazon river sediments, the proportion of Corg solubilised during acid leaching was relatively constant with average values of 14 and 19 % respectively. Thus, it is possible to correct the Corg content for the dissolved organic carbon content measured after decarbonation. Data presented here show that Corg dissolved during liquid acid leaching must be taken into account. After careful calibration, the method presented here should, therefore, be applied to any carbonate-rich detrital sediment. La détermination de la teneur totale en carbone organique et de sa composition dans des sédiments détritiques requiert leur décarbonatation préalable. l'élimination complète de carbonates tels que la dolomite ne peut être réalisée qu'au moyen d'une attaque avec un acide en phase liquide ce qui peut entrainer la solubilisation d'une partie du carbone organique. Pour un ensemble de sédiments détritiques provenant du système Himalayen et de l'Amazone ainsi que pour cinq matériaux géologiques de référence, nous avons déterminé la proportion de carbone organique (Corg) solubilisé lors de la décarbonatation. Celle-ci est significative pour l'ensemble des sédiments analysés et tend à augmenter avec la teneur en carbone organique. En comparaison avec les autres types de sédiments analysés, les fractions argileuses extraites de sédiments de rivière et les sédiments de fond très pauvres en Corg ont une proportion de Corg soluble dans l'acide respectivement élevée et faible. Dans les sédiments himalayens et amazoniens, la proportion de Corg solubilisé lors de la décarbonatation est plutôt constante avec des valeurs moyennes respectives de 14 et 19%. Nous pouvons donc calculer avec précision la teneur totale en carbone organique à partir de la teneur en Corg déterminée après décarbonatation. Nos données montrent que la solubilisation de Corg lors de la décarbonatation par un acide en solution est importante et doit être prise en compte lors de la détermination de la teneur en carbone organique. Moyennant une calibration minutieuse, la méthode que nous présentons devrait donc être utilisée pour l'analyse de sédiments détritiques riches en carbonates. [source]


    Contaminant Transport in Fractured Chalk: Laboratory and Field Experiments

    GROUND WATER, Issue 6 2003
    K. Witthüser
    Laboratory experiments were performed on chalk samples from Denmark and Israel to determine diffusion and distribution coefficients. Batch tests were used to define sorption isotherms for naphthalene and o-xylene. Linear sorption isotherms were observed and described with Henry-isotherms. Because of the high purity and low contents of clay minerals and organic carbon, Danish and white Israeli chalk generally have low retardation capacities. Con-trarily, gray Israeli chalk, with organic carbon fractions as high as 1.092%, remarkably retards organic contaminants. The Koc concept is not applicable to predicting distribution coefficients based on the organic carbon content in the chalk samples. Effective diffusivities of o -xylene, naphthalene, and several artificial tracers were determined using through-diffusion experiments. Based on measured diffusion coefficients and available literature values, a chalk specific exponent of 2.36 for Archie's law was derived, allowing a satisfactory estimate of relative diffusivities in chalk. A field-scale tracer test with uranine and lithium was performed in the Negev desert (Israel) to examine the transfer-ability of diffusivities determined on small rock samples in the laboratory. Due to low recovery rates of the tracer, a modified single fissure dispersion model was used for inverse modeling of the breakthrough curves. Resulting diffusivities deviate insignificantly from the laboratory values, which are considered to be representative for the investigated part of the aquifer and applicable in transport models. [source]


    Retardation of Organic Contaminants in Natural Fractures in Chalk

    GROUND WATER, Issue 3 2002
    A. Wefer-Roehl
    Transport of a conservative compound and two sorbing compounds through fractured chalk was studied using flow-through columns consisting of chalk cores with a single subvertical fracture. Two types of chalk matrix were compared, an oxidized white chalk with low organic carbon content (0.2%), and a gray chalk with a higher organic carbon content (1.3%). Initial rapid breakthrough followed by a delayed approach to a relative concentration of unity for the conservative compound (2,6,difluorobenzoic acid [DFBA]) was clear evidence for diffusion into the porous chalk matrix. Matrix diffusion of DFBA was apparently much greater in the gray chalk columns than in the white chalk columns. Breakthrough curves (BTCs) of the sorbing compounds (2,4,6,tri-bromophenol [TBP] and ametryn [AME]) were retarded in all cases as compared to the conservative compound. Sorption retardation was far greater in the gray chalk as compared with the white chalk, in good agreement with results from batch sorption experiments. BTCs for the conservative compound were relatively nonhysteretic for both white and gray chalk columns. In contrast, BTCs for the sorbing compounds were hysteretic in all cases, demonstrating that sorption was not at equilibrium before desorp-tion began. These experiments suggest that on a field scale, transport of contaminants through fractures in chalk and other fractured porous media will be attenuated by diffusion and sorption into the matrix. [source]


    Optimization of Full-Scale Permanganate ISCO System Operation: Laboratory and Numerical Studies

    GROUND WATER MONITORING & REMEDIATION, Issue 4 2008
    Jeffrey L. Heiderscheidt
    Laboratory characterization studies, one-dimensional flow-through studies, and numerical model simulations were conducted to examine site conditions and system features that may have adversely affected in situ chemical oxidation (ISCO) performance at the Naval Training Center's (NTC) Operable Unit 4 located in Orlando, Florida, and to identify potential ISCO system modifications to achieve the desired remediation performance. At the NTC site, ISCO was implemented using vertical injection wells to deliver potassium permanganate into a ground water zone for treatment of tetrachloroethylene and its breakdown products. However, oxidant distribution was much more limited than anticipated. Characterization studies revealed that the ground water zone being treated by ISCO was very fine sand with a small effective particle size and low uniformity coefficient, along with a high organic carbon content, high natural oxidant demand (NOD), and a high ground water dissolved solids concentration, all of which contributed to full-scale ISCO application difficulties. These site conditions contributed to injection well permeability loss and an inability to achieve the design oxidant injection flow rate, limiting the actual oxidant distribution at the site. Flow-through experiments demonstrated that more favorable oxidant delivery and distribution conditions are enabled by applying a lower oxidant concentration at a faster delivery rate for a greater number of pore volumes. Numerical simulations, run for a variety of conditions (injection/extraction well flow rates, injected oxidant concentration, amount of NOD present, and NOD oxidation rate), also revealed that low,oxidant concentration injection at a high flow rate is a more effective method to deliver the required mass of oxidant to the target treatment zone. [source]


    Yield, Boll Distribution and Fibre Quality of Hybrid Cotton (Gossypium hirsutum L.) as influenced by Organic and Modern Methods of Cultivation

    JOURNAL OF AGRONOMY AND CROP SCIENCE, Issue 4 2006
    D. Blaise
    Abstract India is the largest cotton-growing country (8.9 million hectares) in the world and most of the area is rain-dependent. Large amount of pesticides are used for the control of sucking pests and lepidopterans. Increasing demand for clean organic fibre has led to an interest in organic cotton. However, information on the effects of organic cultivation on fibre quality is limited. Seed cotton yield and fibre quality (length, strength, micronaire and uniformity) were determined for an organic and modern method of cultivation during 3 years (2002,2003 to 2004,2005) of a 11-year (1994,1995 to 2004,2005) study. Vertical and horizontal distribution of bolls on a cotton plant was also determined in 2003,2004 and 2004,2005. At the end of year 11, soil samples were collected and analysed for soil organic carbon content, water-stable aggregates (%), and mean weight diameter. Averaged over 3 years, an additional 94 kg seed cotton ha,1 was produced in the organic over the modern method of cultivation and the difference was significant. The year × treatment interaction was significant. Seed cotton yield in the organic plots was significantly greater than the modern method of cultivation plots in 2003,2004 because of a well-distributed normal rainfall and low pest incidence. The main stem nodes 13,22 accounted for the largest numbers of bolls present on the plant. Plants of the organic plots had significantly (37,71 %) more bolls on nodes 13,27 than those for the plants of the modern method of cultivation. Lateral distribution of bolls on a sympodial (fruiting) branch, was noticed up to fruiting point 11. However, treatment differences were not significant. With regard to fibre quality (length, strength, fineness and uniformity), differences between years were significant. Inferior quality fibre was produced in 2004,2005 because of delayed planting and early cessation of rain. On average, cotton grown under organic conditions compared with the modern method of cultivation had significantly better fibre length (25.1 vs. 24.0 mm) and strength (18.8 vs. 17.9 g tex,1). Soil samples of the organic plots had significantly greater C content, water-stable aggregates and mean weight diameter than the modern method of cultivation plots. Differences were restricted to the top layers (0,0.1 and 0.1,0.2 m). Yield benefits of growing cotton in an organic system over the modern method of cultivation are expected to be greater in years receiving normal rainfall and having low pest incidence. [source]


    GEOCHEMICAL AND GEOPHYSICAL ANOMALIES AT THE ZDANICE OIL- AND GASFIELD, SE CZECH REPUBLIC

    JOURNAL OF PETROLEUM GEOLOGY, Issue 1 2008
    M. Matolin
    Oil at the Zdanice field in the SE Czech Republic is reservoired at a depth of 900 m in weathered Precambrian granitoids and Lower Miocene sandstones and conglomerates. Tertiary claystones, siltstones and sandstones form the top seal. Surface gamma-ray spectrometry carried out along two profiles across the field (6,880 m and 8,335 m in length, respectively) found perceptible decreases of K, U, and Th concentrations relative to background values. This can be explained in terms of enhanced leaching of these radionuclides by groundwater acids derived from hydrocarbons. Observed increases in radon and thoron in soil gas above the oil-producing zone at Zdanice may be caused by enhanced gas emanation from U- and Th-bearing minerals decomposed by groundwater acids. Laboratory analyses of 444 samples collected from 18 shallow boreholes (20 m deep) pointed to a trend of decreasing K, U and Th concentrations above the oil-producing zone at Zdanice. Decreases in rock porosity and organic carbon content were also noted together with an increase in mineralogical density, magnetic susceptibility and sulphur content. Petrophysical analyses of 330 samples from deep boreholes showed lower values of K and U in samples from oil-producing wells. These observations of minor petrophysical alterations in rocks overlying the Zdanice oilfield may be characteristic and may be applicable to hydrocarbon exploration operations elsewhere. [source]


    BURIAL HISTORY RECONSTRUCTION AND THERMAL MODELLING AT KUH-E MOND, SW IRAN

    JOURNAL OF PETROLEUM GEOLOGY, Issue 4 2003
    M. R. Kamali
    At the Kuh-e Mond anticline (Fars Province, SW Iran) and in nearby offshore structures, large volumes of natural gas are reservoired in the Permian , Early Triassic Dehram Group while heavy oil has been discovered in the Cretaceous Sarvak and Eocene Jahrum Formations. In this paper, we use data from six exploration wells and from nearby surface exposures to reconstruct the burial history at Kuh-e Mond. Regional observations show that the thick sedimentary fill in this part of the Zagros Basin was subjected to intense tectonism during the Zagros Orogeny, with a paroxysmal phase during the late Miocene and Pliocene. Thermal modelling and geochemical data from Kuh-e Mond and adjacent fields allows possible hydrocarbon generation and migration mechanisms to be identified. Maturities predicted using Lopatin's TTI model are in accordance with maturities obtained from vitrinite reflectance measurements. We show that formations which have source potential in the nearby Dezful Embayment (including the Pabdeh, Gurpi, Gadvan and Kazhdumi Formations) have not reached the oil window in the Mond wells. Moreover, their organic carbon content is very low as they were deposited in oxic, shallow-water settings. Underlying units (including the Ordovician and Cambrian) could have reached the gas window but contain little organic matter. Silurian shales (Sarchahan Formation), which generate gas at Kuh-e Gahkum and Kuh-e Faraghan (north of Bandar Abbas) and in Saudi Arabia and elsewhere in the Middle East, are absent from the Mond structure. The absence of source rocks suggests that the gas and heavy oil accumulations at Kuh-e Mond and at nearby fields have most probably undergone long-distance lateral migration from distant source kitchens. [source]


    Wildfire effects on soil erodibility of woodlands in NW Spain

    LAND DEGRADATION AND DEVELOPMENT, Issue 2 2010
    M. E. Varela
    Abstract Knowledge of soil erodibility following wildfire is of crucial importance for prioritisation of post-fire restoration practices for soil erosion mitigation. The present work therefore aims to determine the effect of wildfire on soil erodibility for common woodlands in Galicia, NW Spain. This is done by comparing selected topsoil properties of 28 pairs of recently wildfire-burned and neighbouring unburned sites on different geologic substrates. The soil properties were selected for their supposed importance in erodibility, and include aggregate size distribution and water aggregate stability. Comparison of the burned and unburned sites suggested that wildfire had a noticeable negative effect on aggregate size distribution but not on particle size distribution. The effect on aggregate stability was highly variable. Aggregate stability was clearly lower at the burned than unburned site in about a third of the cases and in the remaining cases either basically the same at both sites or higher at the unburned site. The differences in aggregate stability, like those in aggregate size distribution, appear to be associated with changes in organic carbon content. The impact of wildfire on soil erodibility is supposed to operate through its effect on soil organic matter and, thus, to depend strongly on fire severity. Soil erodibility is then little affected by low-severity wildfires but markedly diminished following high-severity wildfires. All burned topsoils were strongly to very strongly water repellent. Fire-enhaced repellency is therefore viewed as a key factor in the post-fire runoff and erosion processes repeatedly observed in recently burned areas in NW Spain. Copyright © 2009 John Wiley & Sons, Ltd. [source]


    Microbial colonisation of artificial and deep-sea sediments in the Arctic Ocean

    MARINE ECOLOGY, Issue 4 2009
    Corinna Kanzog
    Abstract Although environmental factors such as grain size and organic carbon content may influence the distribution of microbes in marine sediments, there has been little experimental study of the topic to date. To investigate how those sediment variables affect microbial colonisation under in situ conditions, deep-sea sediments and artificial sediments (glass beads, sands) were incubated in the Arctic deep sea at 2500 m water depth with or without chitin, one of the most important carbon polymers in marine environments. Microbial abundance, biomass, chitobiase activity and changes in community structure were monitored after 7 days and 1 year. In control sediments without chitin addition, no significant changes in microbial abundance, biomass and activity were observed after 1 year. In the presence of chitin, however, considerable increases in these parameters were recorded in all three sediment types tested. Regardless of chitin addition, natural deep-sea sediments were always associated with higher values of microbial abundance, biomass and activity compared with artificial sediments. Sediment type was always found to be the most significant factor explaining variation in enzymatic activity and bacterial community structure as compared to the effects of chitin amount, incubation time, and changes in cell number or biomass. Overall, this is the first in situ study that has addressed the effects of multiple factors and their interactions on abundance, biomass, activity and community structure of microbial communities in the deep Arctic Ocean. [source]


    Capacity of model biobeds to retain and degrade mecoprop and isoproturon

    PEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 10 2003
    Vibeke V Henriksen
    Abstract Biobeds are used to increase the adsorption and degradation of pesticide spillage on sites used for mixing and loading and for cleaning of sprayers. The adsorption and the rate of degradation of 14C-labelled isoproturon and mecoprop (MCPP) at concentrations from 0.0005 to 25 000 mg kg,1 were determined in biobed soil. Further leaching of the two herbicides was determined in a model biobed with a surface area of 2 m2. The biobed material showed enhanced ability to adsorb the two herbicides. Kd was 5.2 litre kg,1 for isoproturon and 1.6 litre kg,1 for MCPP in biobed material, which is higher than in natural soil. In different experiments with natural soil, Kd ranges from 0.07 to 0.6 litre kg,1 for MCPP and from 1.5 to 4.6 litre kg,1 for isoproturon in soils with varying organic carbon content. Degradation of MCPP was rapid at concentrations from 0.0005 to 500 mg kg,1, delayed at 5000 mg kg,1, and very slow at 25 000 mg kg,1. For isoproturon, the relative degradation was most rapid at the lowest concentration and decreasing with increasing concentrations. After 120 days, between 55% and 8% 14C was evolved as 14CO2 at concentrations between 0.0005 and 25 000 mg kg,1. The rate of evolution of 14CO2 indicated that degradation rates at low concentrations were of first-order and at higher concentrations of zero-order. Leaching of MCPP and isoproturon was determined in a newly established model biobed during a 2-year period. About 13% of applied MCPP and 1.4% of applied isoproturon leached out during the winter following the first autumn application (worst-case scenario). Leaching was completely prevented when the biobed had a well-developed grass cover and was covered during the winter. Copyright © 2003 Society of Chemical Industry [source]


    Environmental fate of metalaxyl and chlorothalonil applied to a bentgrass putting green under southern California climatic conditions

    PEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 4 2002
    L Wu
    Abstract Putting greens usually receive high inputs of fertilizers and pesticides to meet the high demand for visual quality and to overcome the stress from close mowing and traffic. In this study, two commonly used fungicides, metalaxyl (methyl N -(methoxyacetyl)- N -(2,6-xylyl)- DL -alaninate) and chlorothalonil (2,4,5,6-tetrachloro-1,3-benzenedicarbonitrile), were evaluated for their partitioning and persistence in a bentgrass (Agrostis palustris Huds) putting green under southern California climatic conditions. The putting green site was constructed according to the US Golf Association (USGA) specifications. Lysimeter assemblies installed at the center of each plot were used to monitor the leachate, flux chambers were used to measure volatilization, clippings were collected to determine the residues on grass, and soil cores were sampled to determine residues in the soil profile. Results showed that cumulative volatilization loss accounted for 0.10 and 0.02%, clipping removal 0.11 and 0.13%, and cumulative leaching 0.71 and 0.002% of the applied metalaxyl and chlorothalonil, respectively. The two fungicides were mainly found in the top 10,cm of the soil profile due to the high organic carbon content in the thatch and mat layers. The dissipation half-life was 1.4 days for metalaxyl and 4.9 days for chlorothalonil on grass, shorter than those found in agricultural fields. This study showed that, under normal turf management practices, the offsite transport of the parent fungicides was minimal. Future research should focus on investigating the fate and mobility of the metabolites of the fungicides. © 2002 Society of Chemical Industry [source]


    Effects of tidal flat reclamation on sediment quality and hypoxia in Isahaya Bay

    AQUATIC CONSERVATION: MARINE AND FRESHWATER ECOSYSTEMS, Issue 6 2006
    Yoshikuni Hodoki
    Abstract 1.Ariake Bay, which is located in western Japan, has a large tidal range (>6 m) and a vast tidal flat (200 km2). In the early 1990s, the government-managed Isahaya Reclamation Project began in the western part of Ariake Bay. A 16-km2 area of tidal flat in the inner part of Isahaya Bay was destroyed through reclamation and separated from the sea by a dyke, which created land and a freshwater reservoir. 2.Since the initiation of the project, fishery yields around Isahaya Bay have dramatically decreased. The objective of this study was to clarify the relationship between the work associated with the Isahaya Reclamation Project and the recent environmental deterioration in Ariake Bay, with references to present sediment thickness and organic matter content, and hypoxic water distributions in Isahaya Bay. 3.The organic matter load from the reservoir has increased since the initiation of the reclamation project and has been associated with a thick layer of fine sediment at the bottom of Isahaya Bay. The thickness of fine sediment and the total organic carbon content were higher in Isahaya Bay than in the freshwater reservoir. 4.Based on measurements in August 2001, hypoxic water spread widely in and around Isahaya Bay; the lowest dissolved oxygen (DO) concentration (0.53 mg L,1) was observed just outside the dyke. An analysis based on a two-layered box model using data obtained in August 2001 showed that the DO consumption rate in the bottom layer was high (0.61 mg O2 L,1 day,1), and that 22,41% of the total organic carbon load needed to induce the hypoxic water was derived from the reclamation area. 5.Our findings strongly suggest that enclosed seas may suffer from eutrophic and hypoxic conditions because of their low seawater-exchange rate. A comprehensive conservation programme and environmental assessment including physical and material transport processes in the system is needed to manage the environment of the enclosed sea. Copyright © 2005 John Wiley & Sons, Ltd. [source]


    Labile Phosphorus in Soils of Forest Fallows and Primary Forest in the Bragantina Region, Brazil

    BIOTROPICA, Issue 1 2003
    Jacqueline Frizano
    ABSTRACT We used the Hedley sequential extraction procedure to measure nine different organic inorganic soil phosphorus fractions in forest soil of the Bragantina region of Para, Brazil. We compared the labile fractions (resin-extractable P + HCO3-extractable inorganic and organic P) in Oxisols from three secondary forests (10, 20, and 40 years old) and a primary forest. These stands were located in an area that has supported shifting agriculture for approximately a century. After agricultural use, total P and labile P in soils of young secondary forests are diminished compared to the amounts presents in the primary forest soil. Within each stand, organic carbon content was a good predictor of labile organic and inorganic P, consistent with the large body of research indicating that mineralization of organic matter is important to plant nutrition in tropical ecosystems. During the reorganization of P pools during forest development, the pool of labile organic P (HCO3-extractable) diminishes more than the other labile fractions, suggesting that it is directly or indirectly an important source of P for the regrowing forest vegetation. Across the four age classes of forest, the soil reservoir of labile P was equal to or greater than the total amount of P in the vegetation. If labile P measured by this method adequately represents P available to plants in the short term (as suggested by the current consensus), we would conclude that plant-available P is reasonable abundant, and that the effects of agriculture on available P pools are detectable but not sufficient to compromise forest regrowth in this area. [source]


    Geochemical Signatures of Early Paleogene Source Rocks in the Sanshui Basin, South China

    ACTA GEOLOGICA SINICA (ENGLISH EDITION), Issue 1 2010
    Chunlian LIU
    Abstract: The Honggang member of the early Paleogene Buxin Formation is the main source rock in the Sanshui Basin, characterized by organic-rich black shales with the cyclic recurrence of organic-poor sediments. The geochemical characteristics of the Honggang member have been documented to determine the organic matter types and depositional environments in this paper. The organic matter of the black shales mainly consists of a mixture of land plant-derived and phytoplankton-derived organic matter. Total organic carbon content (TOC)-sulfur-iron (Fe) relationships suggest that the organic-rich black shales were deposited under dysoxic-to-euxinic water conditions. The time that iron minerals remained in contact with H2S in anoxic waters possibly influenced the formation of syngenetic pyrite, and organic carbon controlled the formation of diagenetic pyrite. Organic-poor intervals usually show pyrite sulfur enrichment and higher degree of pyritization values relative to low organic carbon contents. This resulted from HS, diffusing downward from overlying organic-rich sediments and formed Fe sulfides through reactions with sufficient Fe. Trace elements generally exhibit low concentrations and little TOC dependence, suggesting some degree of depletion in these elements in the early Paleogene sediments of the Sanshui Basin. This probably resulted from cyclic recurrences of oxic benthic conditions, which promoted the remobilization of trace elements and caused the low concentration of trace elements. [source]


    Decoloration of acid dye effluent with ozone: effect of pH, salt concentration and treatment time

    COLORATION TECHNOLOGY, Issue 1 2005
    M Muthukumar
    A study of the ozone treatment of textile effluent containing acid dyes has been carried out to explore the influence of their chemistry, and the pH, salt concentration, ozone dose and time of treatment. The experiments were constructed using a Box-Hunter second-order composite design for three variables. The study has demonstrated that the type of aromatic rings and the number of sulphonic acid groups in the dye have a marked effect on decoloration. The pH, salt concentration and treatment time are also found to have a predictable influence. The ozone oxidation of acid dye effluent results in a reduction in pH and total organic carbon content. [source]


    Antioxidants in soil organic matter and in associated plant materials

    EUROPEAN JOURNAL OF SOIL SCIENCE, Issue 2 2009
    D. L. Rimmer
    Summary The presence of antioxidants in soil could have a significant effect on the dynamics of soil organic matter. In this paper we report some preliminary experiments, which demonstrate that antioxidants can be extracted from soils and that the quantities vary from soil to soil. Extraction with 1.0 m NaOH was effective, and this was then used on a range of mineral and organic soils, and the antioxidant capacity of the resulting extracts was measured. The antioxidant capacities obtained were positively correlated with soil carbon contents and with the dissolved organic carbon contents of the extracts. Expressing the data per mass of soil carbon showed that the antioxidants generally decreased with depth in the soil profile, suggesting that they were subject to degradation during humification. In a follow-up study, soil, litter and fresh plant samples were collected from 15 sites with a wide variety of vegetation types and analysed for their antioxidant capacities. The aim was to show that the antioxidant capacities in the soils were related to the antioxidant capacities of the fresh plant material and/or litter above. The antioxidant capacities of the soil samples were less than those in either fresh material or litter. While there was a significant positive relationship between the antioxidant capacities of fresh material and litter, no relationship existed between the antioxidant capacities of the soils and those of either fresh material or litter. [source]


    Gas breakthrough experiments on fine-grained sedimentary rocks

    GEOFLUIDS (ELECTRONIC), Issue 1 2002
    A. Hildenbrand
    Abstract The capillary sealing efficiency of fine-grained sedimentary rocks has been investigated by gas breakthrough experiments on fully water saturated claystones and siltstones (Boom Clay from Belgium, Opalinus Clay from Switzerland and Tertiary mudstone from offshore Norway) of different lithological compositions. Sand contents of the samples were consistently below 12%, major clay minerals were illite and smectite. Porosities determined by mercury injection lay between 10 and 30% while specific surface areas determined by nitrogen adsorption (BET method) ranged from 20 to 48 m2 g , 1. Total organic carbon contents were below 2%. Prior to the gas breakthrough experiments the absolute (single phase) permeability (kabs) of the samples was determined by steady state flow tests with water or NaCl brine. The kabs values ranged between 3 and 550 nDarcy (3 × 10,21 and 5.5 × 10,19 m2). The maximum effective permeability to the gas-phase (keff) measured after gas breakthrough on initially water-saturated samples extended from 0.01 nDarcy (1 × 10,23 m2) up to 1100 nDarcy (1.1 × 10,18 m2). The residual differential pressures after re-imbibition of the water phase, referred to as the ,minimum capillary displacement pressures' (Pd), ranged from 0.06 to 6.7 MPa. During the re-imbibition process the effective permeability to the gas phase decreases with decreasing differential pressure. The recorded permeability/pressure data were used to derive the pore size distribution (mostly between 8 and 60 nm) and the transport porosity of the conducting pore system (10 -5,10 -2%). Correlations could be established between (i) absolute permeability coefficients and the maximum effective permeability coefficients and (ii) effective or absolute permeability coefficients and capillary sealing efficiency. No correlation was found between the capillary displacement pressures determined from gas breakthrough experiments and those derived theoretically by mercury injection. [source]