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Sample records for refractory organic matter

  1. Molecular-level dynamics of refractory dissolved organic matter

    NASA Astrophysics Data System (ADS)

    Niggemann, J.; Gerdts, G.; Dittmar, T.

    2012-04-01

    Refractory dissolved organic matter (DOM) accounts for most of the global oceanic organic carbon inventory. Processes leading to its formation and factors determining its stability are still largely unknown. We hypothesize that refractory DOM carries a universal molecular signature. Characterizing spatial and temporal variability in this universal signature is a key to understanding dynamics of refractory DOM. We present results from a long-term study of the DOM geo-metabolome in the open North Sea. Geo-metabolomics considers the entity of DOM as a population of compounds, each characterized by a specific function and reactivity in the cycling of energy and elements. Ten-thousands of molecular formulae were identified in DOM by ultrahigh resolution mass spectrometry analysis (FT-ICR-MS, Fourier-Transform Ion Cyclotron Resonance Mass Spectrometry). The DOM pool in the North Sea was influenced by a complex interplay of processes that produced, transformed and degraded dissolved molecules. We identified a stable fraction in North Sea DOM with a molecular composition similar to deep ocean DOM. Molecular-level changes in this stable fraction provide novel information on dynamics and interactions of refractory DOM.

  2. Detecting refractory organic matter on Mars: how derivatization will help

    NASA Astrophysics Data System (ADS)

    Freissinet, C.; Kashyap, S.; Glavin, D. P.; Buch, A.; Brault, A.; Mahaffy, P. R.

    2012-12-01

    The search for organic molecules on Mars can provide important first clues of extinct or extant biota on the planet. Gas Chromatography Mass Spectrometry (GC-MS) is currently the most relevant space-compatible analytical tool for the detection of organics. Nevertheless, GC separation is intrinsically restricted to volatile molecules, and a lot of the molecules of exobiological interest are refractory or polar. To analyze these organics such as amino acids, nucleobases and carboxylic acids, an additional derivatization step is required to transform them into volatile derivatives that are amenable to GC analysis. As part of the Sample Analysis at Mars (SAM) experiment onboard Mars Science Laboratory (MSL) Curiosity rover which successfully landed on Mars on August 5, 2012, a single-step protocol of extraction and chemical derivatization with the silylating reagent N-methyl-N-(tert-butyldimethylsilyl)-trifluoroacetamide MTBSTFA has been developed to reach a wide range of astrobiology-relevant refractory organic molecules. Seven cups on SAM are devoted to MTBSTFA derivatization. However, this chemical reaction adds a protective silyl group in place of each labile hydrogen, which make the molecule non-identifiable in common mass spectra libraries. We thus created an extended library of mass spectra of derivatized compounds of interest, considering their potential occurrence in Mars soils. We then looked specifically at these compounds using the existing and the newly created library, in various Mars analog soils. To enable a more accurate interpretation of the in situ derivatization GC-MS results that will be obtained by SAM, the lab experiments are performed in the restrictive conditions of the SAM flight instrument. First experiments display promising results, the system permitting an extraction and detection of several proteinic amino and carboxylic acids from Martian representative matrices. Preliminary results show a lack of derivatized organic molecules in

  3. Coupled Ocean-Atmosphere Loss of Refractory Marine Dissolved Organic Matter

    NASA Astrophysics Data System (ADS)

    Kieber, D. J.; Keene, W. C.; Frossard, A. A.; Long, M. S.; Russell, L. M.; Maben, J. R.; Kinsey, J. D.; Tyssebotn, I. M.; Quinn, P.; Bates, T. S.

    2013-12-01

    Marine aerosol produced in the oceans from bursting bubbles and breaking waves is number dominated by submicron aerosol that are highly enriched in marine organic matter relative to seawater. Recent studies suggest that these organic-rich, submicron aerosol have a major impact on tropospheric chemistry and climate. It has been assumed this marine-derived aerosol organic matter is of recent origin stemming from biological activity in the photic zone. However, we deployed a marine aerosol generator on a recent cruise in the Sargasso Sea with seawater collected from 2500 m and showed that the aerosol generated from this seawater was enriched with organic matter to the same level as observed in surface Sargasso seawater, implying that the marine organic matter flux from the oceans into atmospheric aerosol is partly due to marine organic matter not of recent origin. We propose that marine aerosol production and subsequent physical and photochemical atmospheric evolution is the main process whereby old, refractory organic matter is removed from the oceans, thereby closing the carbon budget in the oceans and solving a long-standing conundrum regarding the removal mechanism for this organic matter in the sea. The implications of this study for couplings in the ocean-atmosphere cycling of organic matter will be discussed.

  4. Synthesis of refractory organic matter in the ionized gas phase of the solar nebula.

    PubMed

    Kuga, Maïa; Marty, Bernard; Marrocchi, Yves; Tissandier, Laurent

    2015-06-01

    In the nascent solar system, primitive organic matter was a major contributor of volatile elements to planetary bodies, and could have played a key role in the development of the biosphere. However, the origin of primitive organics is poorly understood. Most scenarios advocate cold synthesis in the interstellar medium or in the outer solar system. Here, we report the synthesis of solid organics under ionizing conditions in a plasma setup from gas mixtures (H2(O)-CO-N2-noble gases) reminiscent of the protosolar nebula composition. Ionization of the gas phase was achieved at temperatures up to 1,000 K. Synthesized solid compounds share chemical and structural features with chondritic organics, and noble gases trapped during the experiments reproduce the elemental and isotopic fractionations observed in primitive organics. These results strongly suggest that both the formation of chondritic refractory organics and the trapping of noble gases took place simultaneously in the ionized areas of the protoplanetary disk, via photon- and/or electron-driven reactions and processing. Thus, synthesis of primitive organics might not have required a cold environment and could have occurred anywhere the disk is ionized, including in its warm regions. This scenario also supports N2 photodissociation as the cause of the large nitrogen isotopic range in the solar system.

  5. Synthesis of refractory organic matter in the ionized gas phase of the solar nebula

    PubMed Central

    Kuga, Maïa; Marty, Bernard; Marrocchi, Yves; Tissandier, Laurent

    2015-01-01

    In the nascent solar system, primitive organic matter was a major contributor of volatile elements to planetary bodies, and could have played a key role in the development of the biosphere. However, the origin of primitive organics is poorly understood. Most scenarios advocate cold synthesis in the interstellar medium or in the outer solar system. Here, we report the synthesis of solid organics under ionizing conditions in a plasma setup from gas mixtures (H2(O)−CO−N2−noble gases) reminiscent of the protosolar nebula composition. Ionization of the gas phase was achieved at temperatures up to 1,000 K. Synthesized solid compounds share chemical and structural features with chondritic organics, and noble gases trapped during the experiments reproduce the elemental and isotopic fractionations observed in primitive organics. These results strongly suggest that both the formation of chondritic refractory organics and the trapping of noble gases took place simultaneously in the ionized areas of the protoplanetary disk, via photon- and/or electron-driven reactions and processing. Thus, synthesis of primitive organics might not have required a cold environment and could have occurred anywhere the disk is ionized, including in its warm regions. This scenario also supports N2 photodissociation as the cause of the large nitrogen isotopic range in the solar system. PMID:26039983

  6. Synthesis of refractory organic matter in the ionized gas phase of the solar nebula.

    PubMed

    Kuga, Maïa; Marty, Bernard; Marrocchi, Yves; Tissandier, Laurent

    2015-06-01

    In the nascent solar system, primitive organic matter was a major contributor of volatile elements to planetary bodies, and could have played a key role in the development of the biosphere. However, the origin of primitive organics is poorly understood. Most scenarios advocate cold synthesis in the interstellar medium or in the outer solar system. Here, we report the synthesis of solid organics under ionizing conditions in a plasma setup from gas mixtures (H2(O)-CO-N2-noble gases) reminiscent of the protosolar nebula composition. Ionization of the gas phase was achieved at temperatures up to 1,000 K. Synthesized solid compounds share chemical and structural features with chondritic organics, and noble gases trapped during the experiments reproduce the elemental and isotopic fractionations observed in primitive organics. These results strongly suggest that both the formation of chondritic refractory organics and the trapping of noble gases took place simultaneously in the ionized areas of the protoplanetary disk, via photon- and/or electron-driven reactions and processing. Thus, synthesis of primitive organics might not have required a cold environment and could have occurred anywhere the disk is ionized, including in its warm regions. This scenario also supports N2 photodissociation as the cause of the large nitrogen isotopic range in the solar system. PMID:26039983

  7. Molecular transformation and degradation of refractory dissolved organic matter in the Atlantic and Southern Ocean

    NASA Astrophysics Data System (ADS)

    Lechtenfeld, Oliver J.; Kattner, Gerhard; Flerus, Ruth; McCallister, S. Leigh; Schmitt-Kopplin, Philippe; Koch, Boris P.

    2014-02-01

    More than 90% of the global ocean dissolved organic carbon (DOC) is refractory, has an average age of 4000-6000 years and a lifespan from months to millennia. The fraction of dissolved organic matter (DOM) that is resistant to degradation is a long-term buffer in the global carbon cycle but its chemical composition, structure, and biochemical formation and degradation mechanisms are still unresolved. We have compiled the most comprehensive molecular dataset of 197 Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) analyses from solid-phase extracted marine DOM covering two major oceans, the Atlantic sector of the Southern Ocean and the East Atlantic Ocean (ranging from 50° N to 70° S). Molecular trends and radiocarbon dating of 34 DOM samples (comprising Δ14C values from -229‰ to -495‰) were combined to model an integrated degradation rate for bulk DOC resulting in a predicted age of >24 ka for the most persistent DOM fraction. First order kinetic degradation rates for 1557 mass peaks indicate that numerous DOM molecules cycle on timescales much longer than the turnover of the bulk DOC pool (estimated residence times of up to ~100 ka) and the range of validity of radiocarbon dating. Changes in elemental composition were determined by assigning molecular formulae to the detected mass peaks. The combination of residence times with molecular information enabled modelling of the average elemental composition of the slowest degrading fraction of the DOM pool. In our dataset, a group of 361 molecular formulae represented the most stable composition in the oceanic environment (“island of stability”). These most persistent compounds encompass only a narrow range of the molecular elemental ratios H/C (average of 1.17 ± 0.13), and O/C (average of 0.52 ± 0.10) and molecular masses (360 ± 28 and 497 ± 51 Da). In the Weddell Sea DOC concentrations in the surface waters were low (46.3 ± 3.3 μM) while the organic radiocarbon was significantly

  8. Redox effects on the microbial degradation of refractory organic matter in marine sediments

    NASA Astrophysics Data System (ADS)

    Reimers, Clare E.; Alleau, Yvan; Bauer, James E.; Delaney, Jennifer; Girguis, Peter R.; Schrader, Paul S.; Stecher, Hilmar A.

    2013-11-01

    Microbially mediated reduction-oxidation (redox) reactions are often invoked as being the mechanisms by which redox state influences the degradation of sedimentary organic matter (OM) in the marine environment. To evaluate the effects of elevated, oscillating and reduced redox potentials on the fate of primarily aged, mineral-adsorbed OM contained in continental shelf sediments, we used microbial fuel cells to control redox state within and around marine sediments, without amending the sediments with reducing or oxidizing substances. We subsequently followed electron fluxes in the redox elevated and redox oscillating treatments, and related sediment chemical, isotopic and bacterial community changes to redox conditions over a 748-day experimental period. The electron fluxes of the elevated and oscillating redox cells were consistent with models of organic carbon (OC) oxidation with time-dependent first-order rate constants declining from 0.023 to 0.005 y-1, in agreement with rate constants derived from typical OC profiles and down core ages of offshore sediments, or from sulfate reduction rate measurements in similar sediments. Moreover, although cumulative electron fluxes were higher in the continuously elevated redox treatment, incremental rates of electron harvesting in the two treatments converged over the 2 year experiment. These similar rates were reflected in chemical indicators of OM metabolism such as dissolved OC and ammonia, and particulate OC concentrations, which were not significantly different among all treatments and controls over the experimental time-scale. In contrast, products of carbonate and opal dissolution and metal mobilization showed greater enrichments in sediments with elevated and oscillating redox states. Microbial community composition in anode biofilms and surrounding sediments was assessed via high-throughput 16S rRNA gene sequencing, and these analyses revealed that the elevated and oscillatory redox treatments led to the

  9. Simple and simultaneous determination of glutathione, thioacetamide and refractory organic matter in natural waters by DP-CSV.

    PubMed

    Pernet-Coudrier, Benoît; Waeles, Matthieu; Filella, Montserrat; Quentel, François; Riso, Ricardo D

    2013-10-01

    Although reduced sulphur substances, such as thiol compounds, contain extremely reactive functional groups in the cell, and influence metal speciation and solubility, very few techniques have been developed to quantify such substances in natural waters. In this paper we present a novel method that allows for the simultaneous identification and quantification of glutathione (GSH), thioacetamide-like compounds (TA), and refractory organic matter (ROM) by differential pulse cathodic stripping voltammetry (DP-CSV). Organic compounds are initially deposited on a mercury drop electrode at 0.000 V, pH 1.95, in the presence of ~200 nmol L(-1) Mo(VI), and then stripped, creating reduction peak currents at specific potentials. Using a 60-s deposition time, limits of detection (LODs) are 1 nmol L(-1), 81 nmol L(-1) and 14 μg C L(-1) for GSH, TA and ROM, respectively. By increasing the deposition time to 300 s, LOD is decreased to 0.2 nmol L(-1), 22 nmol L(-1) and 2 μg C L(-1), respectively. This method has a number of advantages in terms of its rapidity, low cost, and relative simplicity (due to the lack of derivatization and pre-concentration steps) and is also an effective method for simultaneously analysing GSH, TA and ROM in water. When not mixed in solution, GSH, L-cysteine and N-acetyl-L-cysteine, as well as TA-like compounds and thiourea, can be detected and identified by measuring their peak potential and standard addition, due to the acidic pH, which also allows for a longer preservation of the filtered sample. The new method described in this paper was tested along an entire river-seawater gradient of the Aulne Estuary (Brittany, France) to assess its capability in terms of determining these natural organic compounds in various surface waters.

  10. CONDENSED MATTER: STRUCTURAL, MECHANICAL, AND THERMAL PROPERTIES: Influence of Selective Edge Removal and Refractory Period in a Self-Organized Critical Neuron Model

    NASA Astrophysics Data System (ADS)

    Lin, Min; Zhao, Gang; Chen, Tian-Lun

    2009-08-01

    A simple model for a set of integrate-and-fire neurons based on the weighted network is introduced. By considering the neurobiological phenomenon in brain development and the difference of the synaptic strength, we construct weighted networks develop with link additions and followed by selective edge removal. The network exhibits the small-world and scale-free properties with high network efficiency. The model displays an avalanche activity on a power-law distribution. We investigate the effect of selective edge removal and the neuron refractory period on the self-organized criticality of the system.

  11. Self-Organizing Maps with Refractory Periods

    SciTech Connect

    Neme, Antonio; Mireles, Victor

    2008-11-06

    Self-organizing map (SOM) has been studied as a model of map formation in the brain cortex. However, the original model present several oversimplifications. For example, neurons in the cortex present a refractory period in which they are not able to be activated, restriction that should be included in the SOM if a better model is to be achieved. Although several modifications have been studied in order to include this biological restriction to the SOM, they do not reflect biological plausibility. Here, we present a modification in the SOM that allows neurons to enter a refractory period (SOM-RP) if they are the best matching unit (BMU) or if they belong to its neighborhood. This refractory period is the same for all affected neurons, which contrasts with previous models. By including this biological restriction, SOM dynamics resembles in more detail the behavior shown by the cortex, such as non-radial activity patterns and long distance influence, besides the refractory period. As a side effect, two error measures are lower in maps formed by SOM-RP than in those formed by SOM.

  12. Removal of High -Concentration and Refractory Organic Matter from Diosgenin Manufacture Wastewater : a case study of a demonstration project in Hubei Province, P R China

    NASA Astrophysics Data System (ADS)

    Bao, J.; Wang, L.

    2009-12-01

    Wastewater from diosgenin manufacture is dark brown (3,500 ~4,000 times of the chroma) and acidic(pH=0.8~1.5)with high concentration of organic matter(COD=25,000~38,000 mg/L)and poor biodegradability(BOD5/COD= 0.25~0.30). It is highly toxic to biota due to the water-soluble saponin, tannins and pectin. Therefore removal of the organic matter is of great importance before the discharge of the wastewater into the environment. Here we presented a set of data from a demonstration project in Hubei province, P R China with an improved technics. This technics, focusing on the treatment of diosgenin wastewater, included hydrolytic acidification, internal electrolysis, neutralization, aerating-improved Up-flow Anaerobic Sludge Bed (UASB) and bio-contact oxidation treatment in sequence to remove the organic matter. After 60 days of starting-up, the water quality from hydrolytic acidification reactor was greatly improved. The effluent became clear, indicating the obvious removal of suspended solids in the water; the ratio of BOD/COD increased to 0.44, suggesting an significant increase of biodegradability; the content of volatile fatty acid (VFA) increased from 22.6 mmol/L to 86.8 mmol/L and the volume loading of COD reached 9.48 kg COD/(m3d). Basically at this stage the removal efficiency of COD was stabilized at 25%. Further treatment was conducted on the effluent from hydrolytic acidification reactor through the Improved UASB Reactor after the internal electrolysis and neutralization. The Improved UASB Reactor can start up at room temperature with an influent of 1,500 mg/L COD and inflow rate of 50(m3/d). Then, temperature was increased gradually to 38 oC (± 2 oC) to optimize the growth of the mesophilic anaerobes in the reactor. The content of VFA of the effluent was controlled below 8 mmol/L to guarantee the pH in the range of 6.8~7.2. After 150 days of debugging, the COD of the influent to UASB increased to 9,600 mg/L, hydraulic retaining time (HRT) was around 70 hrs

  13. Sulfides and refractory organic matter at the surface of 67P/Churyumov-Gerasimenko: evidence from VIRTIS data and laboratory measurements

    NASA Astrophysics Data System (ADS)

    Rousseau, Batiste; Érard, Stéphane; Beck, Pierre; Quirico, Eric; Schmitt, Bernard; Bonal, Lydie; Montes-Hernandez, German; Moroz, Lyuba; Kappel, David; Markus, Kathrin; Arnold, Gabriele; Ciarniello, Mauro; Raponi, Andrea; Longobardo, Andrea; Capaccioni, Fabrizio; Filacchione, Gianrico; Bockelee-Morvan, Dominique; Leyrat, Cedric; Rosetta VIRTIS Team

    2016-10-01

    From Aug. 2014 to Sept. 2016, Rosetta has been orbiting comet 67P and has obtained informations on the origin and evolution of comets. The imaging spectrometer VIRTIS collected reflectance spectra of the surface within the range 0.25-5.1 µm that revealed a low albedo and a homogeneous surface (Capaccioni et al., 2015; Ciarniello et al., 2015). The spectra are also characterized by red slopes in the visible and in the near infrared. These properties have been interpreted to be due to the presence of an organic polyaromatic material mixed with opaque minerals, presumably troilite-like sulfides according to the composition of presumed cometary grains (Quirico et al., 2016).In order to test this proposition, we have run a series of experimental measurements of granular mixtures of an analog of cometary polyaromatic organic matter (an immature coal) and different sulfides (pyrite, pyrrhotite and troilite). Bi-directional reflectance spectra were obtained at IPAG in the range 0.4-4 µm and under a range of viewing geometries. For the first time we are performing measurements on materials with sub-micrometer grains relevant to what is expected for cometary grains. Produced with a planetary grinder operating on colloidal solutions, these grains were characterized with SEM, X-ray diffraction and an electronic microprobe.The experiment confirms that the low albedo in the near infrared is controlled by the abundance of pyrrhotite or troilite, while pyrite is not a viable candidate. These sulfides also account very well for the red slopes in the visible and the near infrared ranges. Excellent match with VIRTIS spectra is obtained for coal+pyrrhotite mixtures with a pyrrhotite abundance ranging from 30 to 50 wt%. Although the cometary grains composition include silicates and other organic compounds (see IDPs and Wild2 samples analysis), these results offer another interpretation of the reddish nature of some small bodies' surfaces, which has been interpreted so far as the

  14. Refractory dissolved organic nitrogen accumulation in high-elevation lakes.

    PubMed

    Goldberg, S J; Ball, G I; Allen, B C; Schladow, S G; Simpson, A J; Masoom, H; Soong, R; Graven, H D; Aluwihare, L I

    2015-01-01

    The role of dissolved organic matter (DOM) as either a sink for inorganic nutrients or an additional nutrient source is an often-neglected component of nutrient budgets in aquatic environments. Here, we examined the role of DOM in reactive nitrogen (N) storage in Sierra Nevada (California, USA) lakes where atmospheric deposition of N has shifted the lakes toward seasonal phosphorus (P)-limitation. Nuclear magnetic resonance (NMR) spectroscopy and isotope analyses performed on DOM isolated from Lake Tahoe reveal the accumulation of refractory proteinaceous material with a 100-200-year residence time. In contrast, smaller lakes in the same watershed contain DOM with typical terrestrial characteristics, indicating that proteins in Lake Tahoe are autochthonously produced. These data support the role of DOM as a possible sink for reactive N in these lake ecosystems and identify a potential role for DOM in affecting the inorganic nutrient stoichiometry of these environments. PMID:25704539

  15. soil organic matter fractionation

    NASA Astrophysics Data System (ADS)

    Osat, Maryam; Heidari, Ahmad

    2010-05-01

    Carbon is essential for plant growth, due to its effects on other soil properties like aggregation. Knowledge of dynamics of organic matter in different locations in the soil matrix can provide valuable information which affects carbon sequestration and soil the other soil properties. Extraction of soil organic matter (SOM) fractions has been a long standing approach to elucidating the roles of soil organic matter in soil processes. Several kind fractionation methods are used and all provide information on soil organic matter function. Physical fractionation capture the effects on SOM dynamics of the spatial arrangement of primary and secondary organomineral particles in soil while chemical fractionation can not consider the spatial arrangement but their organic fractions are suitable for advanced chemical characterization. Three method of physical separation of soil have been used, sieving, sedimentation and densitometry. The distribution of organic matter within physical fractions of the soil can be assessed by sieving. Sieving separates soil particles based strictly on size. The study area is located on north central Iran, between 35° 41'- 36° 01' N and 50° 42'- 51° 14' E. Mean annual precipitation about 243.8 mm and mean annual air temperature is about 14.95 °C. The soil moisture and temperature regime vary between aridic-thermic in lower altitudes to xeric-mesic in upper altitudes. More than 36 surface soil samples (0-20 cm) were collected according to land-use map units. After preliminary analyzing of samples 10 samples were selected for further analyses in five size fractions and three different time intervals in September, January and April 2008. Fractionation carried out by dry sieving in five classes, 1-2 mm, 0.5-1 mm, 270 μm-0.5mm, 53-270 μm and <53 μm. Organic matter and C/N ratio were determined for all fractions at different time intervals. Chemical fractionation of organic matter also carried out according to Tan (2003), also Mineralogical

  16. Environmental factors regulating soil organic matter chlorination

    NASA Astrophysics Data System (ADS)

    Svensson, Teresia; Montelius, Malin; Reyier, Henrik; Rietz, Karolina; Karlsson, Susanne; Lindberg, Cecilia; Andersson, Malin; Danielsson, Åsa; Bastviken, David

    2016-04-01

    Natural chlorination of organic matter is common in soils. Despite the widespread abundance of soil chlorinated soil organic matter (SOM), frequently exceeding soil chloride abundance in surface soils, and a common ability of microorganisms to produce chlorinated SOM, we lack fundamental knowledge about dominating processes and organisms responsible for the chlorination. To take one step towards resolving the terrestrial chlorine (Cl) puzzle, this study aims to analyse how environmental factors influence chlorination of SOM. Four factors were chosen for this study: soil moisture (W), nitrogen (N), chloride (Cl) and organic matter quality (C). These factors are all known to be important for soil processes. Laboratory incubations with 36Cl as a Cl tracer were performed in a two soil incubation experiments. It was found that addition of chloride and nitrogen seem to hamper the chlorination. For the C treatment, on the other hand, the results show that chlorination is enhanced by increased availability of labile organic matter (glucose and maltose). Even higher chlorination was observed when nitrogen and water were added in combination with labile organic matter. The effect that more labile organic matter strongly stimulated the chlorination rates was confirmed by the second separate experiment. These results indicate that chlorination was not primarily a way to cut refractory organic matter into digestible molecules, representing one previous hypothesis, but is related with microbial metabolism in other ways that will be further discussed in our presentation.

  17. The Stable and Radio- Carbon Isotopic Content of Labile and Refractory Carbon in Atmospheric Particulate Matter

    NASA Astrophysics Data System (ADS)

    McNichol, A. P.; Rosenheim, B. E.; Gerlach, D. S.; Hayes, J. M.

    2006-12-01

    Studies of the isotopic content of atmospheric particulate matter are hampered by difficulties in chemically defining the pools of carbon and analytically isolating the different pools. We are conducting studies on reference materials and atmospheric aerosol samples to develop a method to measure stable and radio- carbon isotopes on the labile and refractory carbon. We are using a flow-through combustion system that allows us to combust, collect and measure the isotopic content of the gases produced at all stages of heating/oxidizing. We compare our results to those measured using a chemothermal oxidation method (CTO) (Gustafsson et al., 2001). In this method, refractory carbon is defined as the material remaining after pre- combusting a sample at 375°C in the presence of oxygen for 24 hours. The reference materials are diesel soot, apple leaves and a hybrid of the two (DiesApple), all from NIST. These provide carbon with two well-defined fractions -- the soot provides refractory carbon that is radiocarbon dead and the apple leaves provide organic carbon that is radiocarbon modern. Radiocarbon results from DiesApple indicate that the "refractory" carbon defined by the CTO method is actually a mixture of old and modern carbon that contains over 25% modern carbon. This suggests that charred material formed from the apples leaves during the pre-combustion step is contributing to the fraction we identify as refractory carbon. We are studying this by analyzing the individual materials and the mixture using our flow-through system. First results with this system indicate that the refractory fraction trapped from the DiesApple contains much less modern carbon than the CTO method, less than 7%. We will present detailed concentration and isotopic results of the generation of carbon dioxide during programmed combustion of each of the reference materials. We studied the radiocarbon content of both the total carbon (TC) and refractory carbon in the fine particulate matter (PM

  18. Is old organic matter simple organic matter?

    NASA Astrophysics Data System (ADS)

    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.

  19. [Refractory cardiac arrest patients in prehospital care, potential organ donors].

    PubMed

    Le Jan, Arnaud; Dupin, Aurélie; Garrigue, Bruno; Sapir, David

    2016-09-01

    Under the authority of the French Biomedicine Agency, a new care pathway integrates refractory cardiac arrest patients into a process of organ donation. It is a medical, logistical and ethical challenge for the staff of the mobile emergency services. PMID:27596502

  20. Coupled ocean-atmosphere loss of marine refractory dissolved organic carbon

    NASA Astrophysics Data System (ADS)

    Kieber, David J.; Keene, William C.; Frossard, Amanda A.; Long, Michael S.; Maben, John R.; Russell, Lynn M.; Kinsey, Joanna D.; Tyssebotn, Inger Marie B.; Quinn, Patricia K.; Bates, Timothy S.

    2016-03-01

    The oceans hold a massive quantity of organic carbon, nearly all of which is dissolved and more than 95% is refractory, cycling through the oceans several times before complete removal. The vast reservoir of refractory dissolved organic carbon (RDOC) is a critical component of the global carbon cycle that is relevant to our understanding of fundamental marine biogeochemical processes and the role of the oceans in climate change with respect to long-term storage and sequestration of atmospheric carbon dioxide. Here we show that RDOC includes surface-active organic matter that can be incorporated into primary marine aerosol produced by bursting bubbles at the sea surface. We propose that this process will deliver RDOC from the sea surface to the atmosphere wherein its photochemical oxidation corresponds to a potentially important and hitherto unknown removal mechanism for marine RDOC.

  1. Land Application of Wastes: An Educational Program. Organic Matter - Module 17, Objectives, and Script.

    ERIC Educational Resources Information Center

    Clarkson, W. W.; And Others

    This module sketches out the impact of sewage organic matter on soils. For convenience, that organic matter is separated into the readily decomposable compounds and the more resistant material (volatile suspended solids, refractory organics, and sludges). The fates of those organics are reviewed along with loading rates and recommended soil…

  2. Organic Matter Management

    SciTech Connect

    Izaurralde, Roberto C.; Cerri, Carlos C.

    2002-01-01

    Soil organic matter (S)M) is an essential attribute of soil quality with a key role in soil conservation and sustainable agriculture. Many practices-some involving land use changes-have been shown to increase SOM and thus received considerable attention for their possible role in climate change mitigation. Carbon sequestration in managed soils occurs when there is a net removal of atmospheric CO2 because of the balance between carbon inputs (net primary productivity) and outputs (soil respiration, management-related C emissions). Soil C sequestration has the additional appeal that all its practices conform to principles of sustainable agriculture (e.g., reduced tillage, erosion control, diverse cropping systems, improved soil fertility). Long-term field experiments have been instrumental to increase our understanding of SOM dynamics. This chapter presents fundamental concepts to guide readers on the role of SOM in sustainable agriculture and climate change mitigation.

  3. Arctic River organic matter transport

    NASA Astrophysics Data System (ADS)

    Raymond, Peter; Gustafsson, Orjan; Vonk, Jorien; Spencer, Robert; McClelland, Jim

    2016-04-01

    Arctic Rivers have unique hydrology and biogeochemistry. They also have a large impact on the Arctic Ocean due to the large amount of riverine inflow and small ocean volume. With respect to organic matter, their influence is magnified by the large stores of soil carbon and distinct soil hydrology. Here we present a recap of what is known of Arctic River organic matter transport. We will present a summary of what is known of the ages and sources of Arctic River dissolved and particulate organic matter. We will also discuss the current status of what is known about changes in riverine organic matter export due to global change.

  4. Identification of Reactive and Refractory Components of Dissolved Organic Nitrogen by FT-ICR Mass Spectrometry

    NASA Astrophysics Data System (ADS)

    Cooper, W. T.; Podgorski, D. C.; Osborne, D. M.; Corbett, J.; Chanton, J.

    2010-12-01

    Dissolved organic nitrogen is an often overlooked but potentially significant bioavailable component of dissolved organic matter. Studies of bulk DON turnover have been reported, but the compositions of the reactive and refractory components of DON are largely unknown. Here we show the unique ability of atmospheric pressure photoionization (APPI) coupled to ultrahigh resolution mass spectrometry to identify the reactive and refractory components of DON. Figure 1 is an isolated 0.30 m/z window from an ultrahigh resolution APPI FT-ICR mass spectrum of DON in surface waters draining an agricultural area in South Florida. Using this optimized, negative-ion APPI strategy we have been able to identify the reactive and refractory components of DON in these nitrogen-rich waters. Similar results were observed with samples from soil porewaters in sedge-dominated fens and sphagnum-dominated bogs within the Glacial Lake Agassiz Peatlands (GLAP) of northern Minnesota. Surprisingly, microbes appear to initially use similar enzymatic pathways to degrade DON and DOC, often with little release of nitrogen. Figure 1. Isolated 0.30 m/z window at nominal mass 432 from negative-ion APPI FT-ICR mass spectrum of DOM from waters draining an agricultural area in South Florida. Peaks marked contain nitrogen.

  5. Biodesulfurization of refractory organic sulfur compounds in fossil fuels.

    PubMed

    Soleimani, Mehran; Bassi, Amarjeet; Margaritis, Argyrios

    2007-01-01

    The stringent new regulations to lower sulfur content in fossil fuels require new economic and efficient methods for desulfurization of recalcitrant organic sulfur. Hydrodesulfurization of such compounds is very costly and requires high operating temperature and pressure. Biodesulfurization is a non-invasive approach that can specifically remove sulfur from refractory hydrocarbons under mild conditions and it can be potentially used in industrial desulfurization. Intensive research has been conducted in microbiology and molecular biology of the competent strains to increase their desulfurization activity; however, even the highest activity obtained is still insufficient to fulfill the industrial requirements. To improve the biodesulfurization efficiency, more work is needed in areas such as increasing specific desulfurization activity, hydrocarbon phase tolerance, sulfur removal at higher temperature, and isolating new strains for desulfurizing a broader range of sulfur compounds. This article comprehensively reviews and discusses key issues, advances and challenges for a competitive biodesulfurization process.

  6. Natural organic matter properties in Swedish agricultural streams

    NASA Astrophysics Data System (ADS)

    Bieroza, Magdalena; Kyllmar, Katarina; Bergström, Lars; Köhler, Stephan

    2016-04-01

    We have analysed natural organic matter (NOM) properties in 18 agricultural streams in Sweden covering a broad range of environmental (climate, soil type), land use and water quality (nutrient and concentrations, pH, alkalinity) characteristics. Stream water samples collected every two weeks within an ongoing Swedish Monitoring Programme for Agriculture have been analysed for total/dissolved organic carbon, absorbance and fluorescence spectroscopy. A number of quantitative and qualitative spectroscopic parameters was calculated to help to distinguish between terrestrially-derived, refractory organic material and autochthonous, labile material indicative of biogeochemical transformations of terrestrial NOM and recent biological production. The study provides insights into organic matter properties and carbon budgets in agricultural streams and improves understanding of how agricultural catchments transform natural and anthropogenic fluxes of organic matter and nutrients to signals observed in receiving waters.

  7. Interstellar organic matter in meteorites

    NASA Technical Reports Server (NTRS)

    Yang, J.; Epstein, S.

    1983-01-01

    Deuterium-enriched hydrogen is present in organic matter in such meteorites as noncarbonaceous chondrites. The majority of the unequilibrated primitive meteorites contain hydrogen whose D/H ratios are greater than 0.0003, requiring enrichment (relative to cosmic hydrogen) by isotope exchange reactions taking place below 150 K. The D/H values presented are the lower limits for the organic compounds derived from interstellar molecules, since all processes subsequent to their formation, including terrestrial contamination, decrease their D/H ratios. In contrast, the D/H ratios of hydrogen associated with hydrated silicates are relatively uniform for the meteorites analyzed. The C-13/C-12 ratios of organic matter, irrespective of D/H ratio, lie well within those observed for the earth. Present findings suggest that other interstellar material, in addition to organic matter, is preserved and is present in high D/H ratio meteorites.

  8. INTERACTIONS BETWEEN PHOTOCHEMICAL AND MICROBIAL DECOMPOSITION IN MODIFYING THE BIOLOGICAL AVAILABILITY AND OPTICAL PROPERTIES OF ESTUARINE DISSOLVED ORGANIC MATTER

    EPA Science Inventory

    Direct photodecomposition and photochemically-mediated bacterial degradation (via photochemical modification of otherwise refractory DOM into biologically labile forms) provide
    important pathways for the loss of dissolved organic matter in coastal waters. Here we report
    lab...

  9. Extraterrestrial organic matter: a review.

    PubMed

    Irvine, W M

    1998-10-01

    We review the nature of the widespread organic material present in the Milky Way Galaxy and in the Solar System. Attention is given to the links between these environments and between primitive Solar System objects and the early Earth, indicating the preservation of organic material as an interstellar cloud collapsed to form the Solar System and as the Earth accreted such material from asteroids, comets and interplanetary dust particles. In the interstellar medium of the Milky Way Galaxy more than 100 molecular species, the bulk of them organic, have been securely identified, primarily through spectroscopy at the highest radio frequencies. There is considerable evidence for significantly heavier organic molecules, particularly polycyclic aromatics, although precise identification of individual species has not yet been obtained. The so-called diffuse interstellar bands are probably important in this context. The low temperature kinetics in interstellar clouds leads to very large isotopic fractionation, particularly for hydrogen, and this signature is present in organic components preserved in carbonaceous chondritic meteorites. Outer belt asteroids are the probable parent bodies of the carbonaceous chondrites, which may contain as much as 5% organic material, including a rich variety of amino acids, purines, pyrimidines, and other species of potential prebiotic interest. Richer in volatiles and hence less thermally processed are the comets, whose organic matter is abundant and poorly characterized. Cometary volatiles, observed after sublimation into the coma, include many species also present in the interstellar medium. There is evidence that most of the Earth's volatiles may have been supplied by a 'late' bombardment of comets and carbonaceous meteorites, scattered into the inner Solar System following the formation of the giant planets. How much in the way of intact organic molecules of potential prebiotic interest survived delivery to the Earth has become an

  10. Extraterrestrial organic matter: a review

    NASA Technical Reports Server (NTRS)

    Irvine, W. M.

    1998-01-01

    We review the nature of the widespread organic material present in the Milky Way Galaxy and in the Solar System. Attention is given to the links between these environments and between primitive Solar System objects and the early Earth, indicating the preservation of organic material as an interstellar cloud collapsed to form the Solar System and as the Earth accreted such material from asteroids, comets and interplanetary dust particles. In the interstellar medium of the Milky Way Galaxy more than 100 molecular species, the bulk of them organic, have been securely identified, primarily through spectroscopy at the highest radio frequencies. There is considerable evidence for significantly heavier organic molecules, particularly polycyclic aromatics, although precise identification of individual species has not yet been obtained. The so-called diffuse interstellar bands are probably important in this context. The low temperature kinetics in interstellar clouds leads to very large isotopic fractionation, particularly for hydrogen, and this signature is present in organic components preserved in carbonaceous chondritic meteorites. Outer belt asteroids are the probable parent bodies of the carbonaceous chondrites, which may contain as much as 5% organic material, including a rich variety of amino acids, purines, pyrimidines, and other species of potential prebiotic interest. Richer in volatiles and hence less thermally processed are the comets, whose organic matter is abundant and poorly characterized. Cometary volatiles, observed after sublimation into the coma, include many species also present in the interstellar medium. There is evidence that most of the Earth's volatiles may have been supplied by a 'late' bombardment of comets and carbonaceous meteorites, scattered into the inner Solar System following the formation of the giant planets. How much in the way of intact organic molecules of potential prebiotic interest survived delivery to the Earth has become an

  11. Photodissolution of soil organic matter

    USGS Publications Warehouse

    Mayer, L.M.; Thornton, K.R.; Schick, L.L.; Jastrow, J.D.; Harden, J.W.

    2012-01-01

    Sunlight has been shown to enhance loss of organic matter from aquatic sediments and terrestrial plant litter, so we tested for similar reactions in mineral soil horizons. Losses of up to a third of particulate organic carbon occurred after continuous exposure to full-strength sunlight for dozens of hours, with similar amounts appearing as photodissolved organic carbon. Nitrogen dissolved similarly, appearing partly as ammonium. Modified experiments with interruption of irradiation to include extended dark incubation periods increased loss of total organic carbon, implying remineralization by some combination of light and microbes. These photodissolution reactions respond strongly to water content, with reaction extent under air-dry to fully wet conditions increasing by a factor of 3-4 fold. Light limitation was explored using lamp intensity and soil depth experiments. Reaction extent varied linearly with lamp intensity. Depth experiments indicate that attenuation of reaction occurs within the top tens to hundreds of micrometers of soil depth. Our data allow only order-of-magnitude extrapolations to field conditions, but suggest that this type of reaction could induce loss of 10-20% of soil organic carbon in the top 10. cm horizon over a century. It may therefore have contributed to historical losses of soil carbon via agriculture, and should be considered in soil management on similar time scales. ?? 2011 Elsevier B.V.

  12. The contentious nature of soil organic matter.

    PubMed

    Lehmann, Johannes; Kleber, Markus

    2015-12-01

    The exchange of nutrients, energy and carbon between soil organic matter, the soil environment, aquatic systems and the atmosphere is important for agricultural productivity, water quality and climate. Long-standing theory suggests that soil organic matter is composed of inherently stable and chemically unique compounds. Here we argue that the available evidence does not support the formation of large-molecular-size and persistent 'humic substances' in soils. Instead, soil organic matter is a continuum of progressively decomposing organic compounds. We discuss implications of this view of the nature of soil organic matter for aquatic health, soil carbon-climate interactions and land management.

  13. The contentious nature of soil organic matter.

    PubMed

    Lehmann, Johannes; Kleber, Markus

    2015-12-01

    The exchange of nutrients, energy and carbon between soil organic matter, the soil environment, aquatic systems and the atmosphere is important for agricultural productivity, water quality and climate. Long-standing theory suggests that soil organic matter is composed of inherently stable and chemically unique compounds. Here we argue that the available evidence does not support the formation of large-molecular-size and persistent 'humic substances' in soils. Instead, soil organic matter is a continuum of progressively decomposing organic compounds. We discuss implications of this view of the nature of soil organic matter for aquatic health, soil carbon-climate interactions and land management. PMID:26595271

  14. Synergy of fresh and accumulated organic matter to bacterial growth.

    PubMed

    Farjalla, Vinicius F; Marinho, Claudio C; Faria, Bias M; Amado, André M; Esteves, Francisco de A; Bozelli, Reinaldo L; Giroldo, Danilo

    2009-05-01

    The main goal of this research was to evaluate whether the mixture of fresh labile dissolved organic matter (DOM) and accumulated refractory DOM influences bacterial production, respiration, and growth efficiency (BGE) in aquatic ecosystems. Bacterial batch cultures were set up using DOM leached from aquatic macrophytes as the fresh DOM pool and DOM accumulated from a tropical humic lagoon. Two sets of experiments were performed and bacterial growth was followed in cultures composed of each carbon substrate (first experiment) and by carbon substrates combined (second experiment), with and without the addition of nitrogen and phosphorus. In both experiments, bacterial production, respiration, and BGE were always higher in cultures with N and P additions, indicating a consistent inorganic nutrient limitation. Bacterial production, respiration, and BGE were higher in cultures set up with leachate DOM than in cultures set up with humic DOM, indicating that the quality of the organic matter pool influenced the bacterial growth. Bacterial production and respiration were higher in the mixture of substrates (second experiment) than expected by bacterial production and respiration in single substrate cultures (first experiment). We suggest that the differences in the concentration of some compounds between DOM sources, the co-metabolism on carbon compound decomposition, and the higher diversity of molecules possibly support a greater bacterial diversity which might explain the higher bacterial growth observed. Finally, our results indicate that the mixture of fresh labile and accumulated refractory DOM that naturally occurs in aquatic ecosystems could accelerate the bacterial growth and bacterial DOM removal. PMID:18985269

  15. Formation of analogs of cometary nitrogen-rich refractory organics from thermal degradation of tholin and HCN polymer

    NASA Astrophysics Data System (ADS)

    Bonnet, Jean-Yves; Quirico, Eric; Buch, Arnaud; Thissen, Roland; Szopa, Cyril; Carrasco, Nathalie; Cernogora, Guy; Fray, Nicolas; Cottin, Hervé; Roy, Lena Le; Montagnac, Gilles; Dartois, Emmanuel; Brunetto, Rosario; Engrand, Cécile; Duprat, Jean

    2015-04-01

    Nitrogen-rich refractory organics are scarce phases recovered as a fraction of stratospheric IDPs and constitute the bulk of the organic matter of some ultracarbonaceous Antarctic micrometeorites. They are likely formed under very specific conditions within a nitrogen-rich environment and may provide valuable clues on the origin of the population of interplanetary dusts accreted by Earth. In this study, we produced relevant analogs of such refractory organics characterized in three ultracarbonaceous Antarctic micrometeorites, starting from the carbonization of an HCN polymer and a tholin. Indeed, carbonization is a process that can increase the polyaromatic character toward a structure similar to that observed in these cosmomaterials. Both these precursors were degraded in an Ar atmosphere at 300, 500, 700 and 1000 °C over ∼1 h and characterized by elemental analysis, micro-FTIR and Raman micro-spectroscopy (at 244 and 514 nm excitation wavelengths). Our results show that the precursors evolve along distinct chemical and structural pathways during carbonization and that the influence of the precursor structure is still very strong at 1000 °C. Interestingly, these different carbonization routes appear in the spectral characteristics of the G and D bands of their Raman spectra. Several of the residues present chemical and structural similarities with three recently studied ultracarbonaceous micrometeorites (Dobrica et al. [2011]. Meteorit. Planet. Sci. 46, 1363; Dartois et al. [2013]. Icarus 224, 243) and with N-rich inclusions in stratospheric IDPs. However, the residues do not simultaneously account for the carbon structure (Raman) and the chemical composition (IR, N/C ratio). This indicates that the precursors and/or heating conditions in our experiments are not fully relevant. Despite this lack of full relevancy, the formation of a polyaromatic structure fairly similar to that of UCAMMs and IDPs suggests that the origin of N-rich refractory organics lies in a

  16. Priming of native soil organic matter by pyrogenic organic matter

    NASA Astrophysics Data System (ADS)

    DeCiucies, Silene; Dharmakeerthi, Saman; Whitman, Thea; Woolf, Dominic; Lehmann, Johannes

    2015-04-01

    Priming, in relation to pyrogenic organic matter (PyOM), describes the change in mineralization rate of non-pyrogenic ("native") soil organic matter (nSOM) due to the addition of PyOM. Priming may be 'positive', in that the addition of pyC increases the mineralization rate of native SOM, or 'negative', in that the mineralization rate of nSOM is decreased. Reasons for increased mineralization may include: (i) co-metabolism: microbial decomposition of labile C-additions increases microbial activity, and facilitates additional decomposition of npSOC by active enzymes; (ii) stimulation: substrate additions result in lifted pH, nutrient, oxygen, or water constraints resulting in increased microbial activity. Decreased mineralization may be a result of: (i) inhibition: the opposite of stimulation whereby constraints are aggravated by substrate addition. Substrate addition may also cause inhibition by interfering with enzymes or signaling compounds; (ii) preferential substrate utilization: labile fraction of PyOM additions are preferentially used up by microbes thus causing a decrease in nSOC decomposition; (iii) sorption: organic compounds are adsorbed onto PyOM surfaces, decreasing their rate of mineralization; (iv) stabilization: formation of organo-mineral associations forms stable SOC pools. We have conducted a suite of experiments to investigate these potential interactions. In a seven year long incubation study, PyOM additions increased total OM mineralization for the first 2.5 years, was equal to control after 6.2 years, and was 3% lower after 7.1 years. Cumulative nSOM mineralization was 23% less with the PyOM additions than without, and over 60% of the added PyOM was present in the labile soil fraction after the 7.1 year incubation. Two additional incubation studies, one with and without plants, showed greater nSOM mineralization in the short term and lower nSOM mineralization over the long term. Increased nSOC mineralization due to the presence of plants was

  17. Evaluation of refractory organic removal in combined biological powdered activated carbon--microfiltration for advanced wastewater treatment.

    PubMed

    Seo, G T; Ohgaki, S

    2001-01-01

    Biological powdered activated carbon (BPAC) was incorporated with a microfiltration (MF, 0.2 micron pore size) system to remove the refractory organic matter contained in secondary sewage effluent. A synthetic secondary sewage effluent was used as influent in this study, containing both non-biodegradable organic substances (such as humic acid, lignin sulfonate, tannic acid and arabic gum powder) and biodegradable ones. These refractory organic materials were possibly degraded in contact with microorganisms for 20-27 days. Although humic acid and arabic gum were weakly adsorbed on the activated carbon, they could be effectively removed in the BPAC reactor. The TOC removal at a powdered activated carbon (PAC) concentration of 20 g/L was higher than at 0.5-2 g PAC/L (83% and 66-68%, respectively). The higher removal efficiency was due to the increased rejection at the membrane module in which most of the PAC was accumulated. More than 90% of non-biodegradable compounds removal (detected as E280, UV absorption at 280 nm) occurred in the BPAC reactor. The biological growth parameter b/Y, used in system design, was estimated to be 0.017 d-1. Relatively high permeate flux of 1.88 m/d could be obtained even at higher PAC concentration of 20 g/L.

  18. TOWARD THE FORMATION OF CARBONACEOUS REFRACTORY MATTER IN HIGH TEMPERATURE HYDROCARBON-RICH ATMOSPHERES OF EXOPLANETS UPON MICROMETEOROID IMPACT

    SciTech Connect

    Dangi, Beni B.; Kim, Yong S.; Krasnokutski, Serge A.; Kaiser, Ralf I.; Bauschlicher Jr, Charles W.

    2015-05-20

    We report on laboratory simulation experiments mimicking the chemical processing of model atmospheres of exoplanets containing C3 and C4 hydrocarbons at moderate temperatures of 400 K upon interaction of catalytic surfaces of micrometeoroids. By utilizing an ultrasonic levitator device and heating singly levitated particles under simulated microgravity conditions, Raman spectroscopy is utilized as a non-invasive tool to probe on line and in situ the conversion of C3 and C4 hydrocarbons to refractory carbonaceous matter on the surfaces of levitated particles. Secondary Ion Mass Spectrometry and electron microscopic imaging were also conducted to gain further insight into the elementary composition and structures of the refractories formed. Our results provide compelling evidence that in the presence of a catalytic surface, which can be supplied in the form of micrometeoroids and atmospheric dust particles, hydrocarbon gases present in the atmospheres of exoplanets can be converted to refractory, carbon-rich carbonaceous matter of mainly graphitic structure with a carbon content of at least 90% at elevated temperatures. This finding might explain the low methane to carbon monoxide (CH{sub 4}–CO) ratio in the hot Neptune GJ 436b, where the abundant methane photochemically converts to higher order hydrocarbons and ultimately to refractory graphite-like carbon in the presence of a silicon surface.

  19. Trace the evolution of organic matter in interplanetary objects using residue analogues

    NASA Astrophysics Data System (ADS)

    Danger, G.; Fresneau, A.; Abou Mrad, N.; de Marcellus, P.; Orthous-Daunay, F. R.; Modica, P.; Vuitton, V.; Duvernay, F.; Flandinet, L.; Le Sergeant d'Hendecourt, L.; Thissen, R.; Chiavassa, T.

    2015-10-01

    This contribution focuses on one aspect of our work, which is related to the analysis of refractory residues formed from the UV irradiation and the subsequent warming-up to room temperature of astrophysical ice analogs, the RAHIIA project. The understanding of the chemical composition of these refractory residues, commonly called "yellow stuff", as well as the possible pathways to their formation in astrophysical environments, is an important step to establish what kind of organic matter could be available within interplanetary objects such as comets or asteroids, part of which end up as preserved meteorites on telluric planets.

  20. Tracking the organic refractory component from interstellar dust to comets.

    PubMed

    Greenberg, J M; Li, A

    1999-01-01

    The abundance and composition of complex organic (carbonaceous) material in the interstellar dust is followed as the dust evolves in its cyclic evolution between diffuse and dense clouds. Interstellar extinction, laboratory and space analog experiments, dust infrared absorption spectra, the cosmic abundance of the condensible atoms, and space and ground-based observations of comet dust are used to impose constraints on the organic dust component as mantles on silicate cores.

  1. Refractory Organic Compounds in Enceladus' Ice Grains and Hydrothermal Activity

    NASA Astrophysics Data System (ADS)

    Postberg, F.; Khawaja, N.; Hsu, H. W.; Sekine, Y.; Shibuya, T.

    2015-12-01

    Cassini's Cosmic Dust Analyzer (CDA) generates time-of-flight mass spectra of individual grains impinging on the instruments target-plate. Following the analysis of salt rich ice grains emitted by Enceladus that indicated a salt-water ocean in contact with the moon's rocky core [1,2] a recent CDA analysis of nano-phase silica particles pointed at hydrothermal activity at the moon's rock/water interface [3]. The results imply temperatures above 80 - 90°C and alkaline pH values around 10 reminiscent of alkaline hydrothermal vents on Earth like the Lost City Hydrothermal Field. In this context the compositional analysis of organic components in CDA mass spectra of the ejected ice grains is of particular relevance. A multitude of volatile organic species has already been identified in the gas component of the plume [4]. As expected, we find more complex organic molecules in ice grains than in the gas indicating aromatic species, amines, and carbonyl group species. The composition of organic-bearing ice grains displays a great diversity indicating a variety of different organic species in varying concentrations. Recent spatially resolved CDA in situ measurements inside Enceladus' plume indicate that these organic compounds are especially frequent in 'young' ice grains that have just been ejected by high velocity jets. We investigate the implications of our findings with respect to ice grain formation at the water surface and inside the icy vents. We constrain the generation of organic compounds at the rock/water interface in the light of hydrothermal activity and the potential for the formation of life precursor molecules in Enceladus' ocean. Ref:[1] Postberg et al., Nature 459, 1098-1101 (2009). [2] Postberg et al., Nature 474, 620-622 (2011). [3]. Hsu, Postberg, Sekine et al., Nature, 519, 207-210 (2015). [4] Waite et al., Nature 460, 487-490 (2009).

  2. Chemodestructive fractionation of soil organic matter

    NASA Astrophysics Data System (ADS)

    Popov, A. I.; Rusakov, A. V.

    2016-06-01

    The method of chemodestructive fractionation is suggested to assess the composition of soil organic matter. This method is based on determination of the resilience of soil organic matter components and/or different parts of organic compounds to the impact of oxidizing agents. For this purpose, a series of solutions with similar concentration of the oxidant (K2Cr2O7), but with linearly increasing oxidative capacity was prepared. Chemodestructive fractionation showed that the portion of easily oxidizable (labile) organic matter in humus horizons of different soil types depends on the conditions of soil formation. It was maximal in hydromorphic soils of the taiga zone and minimal in automorphic soils of the dry steppe zone. The portion of easily oxidizable organic matter in arable soils increased with an increase in the rate of organic fertilizers application. The long-lasting agricultural use of soils and burying of the humus horizons within the upper one-meter layer resulted in the decreasing content of easily oxidizable organic matter. It was found that the portion of easily oxidizable organic matter decreases by the mid-summer or fall in comparison with the spring or early summer period.

  3. Molecular characterization of dissolved organic matter (DOM): a critical review.

    PubMed

    Nebbioso, Antonio; Piccolo, Alessandro

    2013-01-01

    Advances in water chemistry in the last decade have improved our knowledge about the genesis, composition, and structure of dissolved organic matter, and its effect on the environment. Improvements in analytical technology, for example Fourier-transform ion cyclotron (FT-ICR) mass spectrometry (MS), homo and hetero-correlated multidimensional nuclear magnetic resonance (NMR) spectroscopy, and excitation emission matrix fluorimetry (EEMF) with parallel factor (PARAFAC) analysis for UV-fluorescence spectroscopy have resulted in these advances. Improved purification methods, for example ultrafiltration and reverse osmosis, have enabled facile desalting and concentration of freshly collected DOM samples, thereby complementing the analytical process. Although its molecular weight (MW) remains undefined, DOM is described as a complex mixture of low-MW substances and larger-MW biomolecules, for example proteins, polysaccharides, and exocellular macromolecules. There is a general consensus that marine DOM originates from terrestrial and marine sources. A combination of diagenetic and microbial processes contributes to its origin, resulting in refractory organic matter which acts as carbon sink in the ocean. Ocean DOM is derived partially from humified products of plants decay dissolved in fresh water and transported to the ocean, and partially from proteinaceous and polysaccharide material from phytoplankton metabolism, which undergoes in-situ microbial processes, becoming refractory. Some of the DOM interacts with radiation and is, therefore, defined as chromophoric DOM (CDOM). CDOM is classified as terrestrial, marine, anthropogenic, or mixed, depending on its origin. Terrestrial CDOM reaches the oceans via estuaries, whereas autochthonous CDOM is formed in sea water by microbial activity; anthropogenic CDOM is a result of human activity. CDOM also affects the quality of water, by shielding it from solar radiation, and constitutes a carbon sink pool. Evidence in support

  4. Dissolved organic matter in anoxic pore waters from Mangrove Lake, Bermuda

    USGS Publications Warehouse

    Orem, W.H.; Hatcher, P.G.; Spiker, E. C.; Szeverenyi, N.M.; Maciel, G.E.

    1986-01-01

    Dissolved organic matter and dissolved inorganic chemical species in anoxic pore water from Mangrove Lake, Bermuda sediments were studied to evaluate the role of pore water in the early diagenesis of organic matter. Dissolved sulphate, titration alkalinity, phosphate, and ammonia concentration versus depth profiles were typical of many nearshore clastic sediments and indicated sulphate reduction in the upper 100 cm of sediment. The dissolved organic matter in the pore water was made up predominantly of large molecules, was concentrated from large quantities of pore water by using ultrafiltration and was extensively tudied by using elemental and stable carbon isotope analysis and high-resolution, solid state 13C nuclear magnetic resonance and infrared spectroscopy. The results indicate that this material has a predominantly polysaccharide-like structure and in addition contains a large amount of oxygen-containing functional groups (e.g., carboxyl groups). The 13C nulcear magnetic resonance spectra of the high-molecular-weight dissolved organic matter resemble those of the organic matter in the surface sediments of Mangrove Lake. We propose that this high-molecular-weight organic matter in pore waters represents the partially degraded, labile organic components of the sedimentary organic matter and that pore waters serve as a conduit for removal of these labile organic components from the sediments. The more refractory components are, thus, selectively preserved in the sediments as humic substances (primarily humin). ?? 1986.

  5. Fecal Microbiota Transplantation for Refractory Clostridium difficile Colitis in Solid Organ Transplant Recipients

    PubMed Central

    Friedman-Moraco, R. J.; Mehta, A. K.; Lyon, G. M.; Kraft, C. S.

    2015-01-01

    Fecal microbiota transplantation (FMT) has been shown to be safe and efficacious in individuals with refractory Clostridium difficile . It has not been widely studied in individuals with immunosuppression due to concerns about infectious complications. We describe two solid organ transplant recipients, one lung and one renal, in this case report that both had resolution of their diarrhea caused by C. difficile after FMT. Both recipients required two FMTs to achieve resolution of their symptoms and neither had infectious complications. Immunosuppressed individuals are at high risk for acquisition of C. difficile and close monitoring for infectious complications after FMT is necessary, but should not preclude its use in patients with refractory disease due to C. difficile . Sequential FMT may be used to achieve cure in these patients with damaged microbiota from antibiotic use and immunosuppression. PMID:24433460

  6. Fecal microbiota transplantation for refractory Clostridium difficile colitis in solid organ transplant recipients.

    PubMed

    Friedman-Moraco, R J; Mehta, A K; Lyon, G M; Kraft, C S

    2014-02-01

    Fecal microbiota transplantation (FMT) has been shown to be safe and efficacious in individuals with refractory Clostridium difficile. It has not been widely studied in individuals with immunosuppression due to concerns about infectious complications. We describe two solid organ transplant recipients, one lung and one renal, in this case report that both had resolution of their diarrhea caused by C. difficile after FMT. Both recipients required two FMTs to achieve resolution of their symptoms and neither had infectious complications. Immunosuppressed individuals are at high risk for acquisition of C. difficile and close monitoring for infectious complications after FMT is necessary, but should not preclude its use in patients with refractory disease due to C. difficile. Sequential FMT may be used to achieve cure in these patients with damaged microbiota from antibiotic use and immunosuppression.

  7. Biodegradability of algal-derived organic matter in a large artificial lake by using stable isotope tracers.

    PubMed

    Lee, Yeonjung; Lee, Bomi; Hur, Jin; Min, Jun-Oh; Ha, Sun-Yong; Ra, Kongtae; Kim, Kyung-Tae; Shin, Kyung-Hoon

    2016-05-01

    In order to understand the biodegradability of algal-derived organic matter, biodegradation experiments were conducted with (13)C and (15)N-labeled natural phytoplankton and periphytic algal populations in experimental conditions for 60 days. Qualitative changes in the dissolved organic matter were also determined using parallel factor analysis and the stable carbon isotopic composition of the hydrophobic dissolved organic matter through the experimental period. Although algal-derived organic matter is considered to be easily biodegradable, the initial amounts of total organic carbon newly produced by phytoplankton and periphytic algae remained approximately 16 and 44 % after 60 days, respectively, and about 22 and 43 % of newly produced particulate nitrogen remained. Further, the dissolved organic carbon derived from both algal populations increased significantly after 60 days. Although the dissolved organic matter gradually became refractory, the contributions of the algal-derived organic matter to the dissolved organic matter and hydrophobic dissolved organic matter increased. Our laboratory experimental results suggest that algal-derived organic matter produced by phytoplankton and periphytic algae could contribute significantly to the non-biodegradable organic matter through microbial transformations. PMID:26780057

  8. Biodegradability of algal-derived organic matter in a large artificial lake by using stable isotope tracers.

    PubMed

    Lee, Yeonjung; Lee, Bomi; Hur, Jin; Min, Jun-Oh; Ha, Sun-Yong; Ra, Kongtae; Kim, Kyung-Tae; Shin, Kyung-Hoon

    2016-05-01

    In order to understand the biodegradability of algal-derived organic matter, biodegradation experiments were conducted with (13)C and (15)N-labeled natural phytoplankton and periphytic algal populations in experimental conditions for 60 days. Qualitative changes in the dissolved organic matter were also determined using parallel factor analysis and the stable carbon isotopic composition of the hydrophobic dissolved organic matter through the experimental period. Although algal-derived organic matter is considered to be easily biodegradable, the initial amounts of total organic carbon newly produced by phytoplankton and periphytic algae remained approximately 16 and 44 % after 60 days, respectively, and about 22 and 43 % of newly produced particulate nitrogen remained. Further, the dissolved organic carbon derived from both algal populations increased significantly after 60 days. Although the dissolved organic matter gradually became refractory, the contributions of the algal-derived organic matter to the dissolved organic matter and hydrophobic dissolved organic matter increased. Our laboratory experimental results suggest that algal-derived organic matter produced by phytoplankton and periphytic algae could contribute significantly to the non-biodegradable organic matter through microbial transformations.

  9. Factors Regulating Soil Organic Matter Chlorination

    NASA Astrophysics Data System (ADS)

    Svensson, T.; Gustavsson, M.; Reyier, H.; Rietz, K.; Karlsson, S.; Göransson, C.; Andersson, M.; Öberg, G.; Bastviken, D.

    2013-12-01

    Natural chlorination of organic matter is a common process in various soils. Despite the widespread abundance of soil organic chlorine, knowledge on the processes and regulation of soil organic matter chlorination are modest. The purpose of this study is to elucidate how environmental factors may influence chlorination of organic matter in soil. Four factors were chosen for this study; water content, and nitrogen, organic carbon, and chloride concentrations. The variables are all known in different ways as important for microbes and transformation of chlorine in soil. The soil was collected from 5-15 cm depth in a coniferous forest southeast of Sweden. To test how the selected factors influenced chlorination of organic matter, we used soil laboratory incubations using 36Cl-chloride as a radioisotopic marker. A multivariate factorial design with two levels of i) soil moisture, ii) chloride amendment, iii) nitrogen amendment, and iv) glucose and maltose addition was used to simultaneously test for possible combination effects for all factors. A known radioactivity of 36chloride was added to the soil samples and incubated with four different factor treatments during an incubation period of 15 and 60 days. This presentation will discuss the results of this study including what combination of factors enhanced or hampered chlorination and thereby discuss previous observed variability of organic chlorine and chloride in soil.

  10. Production of recalcitrant organic matter under the influence of elevated carbon dioxide and temperature.

    PubMed

    Ki, Bomin; Park, Suyoung; Choi, Jung Hyun

    2014-09-01

    The effects of elevated CO2 and temperature on the quantity and quality of dissolved organic carbon (DOC) of wetland sediments were investigated by measuring organic matter decomposition rates and phenolic compounds as target recalcitrant organic matter. Mean rates of anaerobic microbial metabolism were consistently higher both in vegetated sediments and in elevated CO2 and temperature, although the differences were not statistically significant (P < 0.05). Concentrations of phenolic compounds in sediments with vegetation are significantly different (P < 0.05) from those in sediments without vegetation. Regarding the biodegradability of the phenolic compounds, vegetated sediments showed higher concentrations of 2-chlorophenol and 2,4-dimethylphenol under elevated CO2 and temperature conditions, which means that more refractory material can be produced through enhanced organic matter degradation by elevated CO2 and temperature. The produced phenolic compounds can be transported to the freshwater ecosystem and influence the recalcitrance of DOC.

  11. Sediment organic matter content as a confounding factor in toxicity tests with Chironomus tentans

    SciTech Connect

    Lacey, R.; Watzin, M.C.; McIntosh, A.W.

    1999-02-01

    Physicochemical characteristics of sediment unrelated to contaminant levels and bioavailability may influence the outcome of toxicity tests. In particular, sediment organic matter content has the potential to be a confounding factor in toxicity tests using the midge larva Chironomus tentans because the larvae are infaunal and feed on organic matter in the sediments. To examine the possibility, the authors conducted a series of tests using formulated sediments with varying organic matter contents following the standard US Environmental Protection Agency (US EPA) 10-day C. tentans growth and survival protocol. Formulated sediments made with peat moss, {alpha}-cellulose, and maple leaves were tested. An organic-rich natural sediment diluted with formulated sediment to achieve a range of organic matter contents was also examined. In a final experiment, sediments containing each of the four organic matter sources at the same concentration were tested against one another. Survival was not greatly affected by concentration of organic matter, except at the lowest concentrations in natural sediment, where survival dipped below 70%. In experiments using peat moss, {alpha}-cellulose, and maple leaves, significant differences in C. tentans growth were found at different organic matter concentrations. In contrast, concentration of organic matter in the natural sediment dilution series had little effect on growth, perhaps because much of this material was highly refractory. In the comparison experiment, growth differed significantly among the four sediments, with best growth achieved with {alpha}-cellulose and leaves. These results suggest that both organic matter quantity and quality can be confounding factors in toxicity tests using C. tentans.

  12. From microbial biomass compounds to non-living soil organic matter - Microbial biomass as a significant source for soil organic matter formation

    NASA Astrophysics Data System (ADS)

    Miltner, A.; Kindler, R.; Hoffmann-Jäniche, C.; Schmidt-Brücken, B.; Kästner, M.

    2009-04-01

    Soil organic matter is one of the most important pools of the global carbon cycle. Recently, it has been suggested that microbial biomass is a significant source for the formation of refractory organic matter. We tested the relevance of this source by incubation of soil with 13C-labeled Escherichia coli cells. We traced the labeled carbon in fatty acids and amino acids, both in the microbial biomass and in the bulk soil. We also localized cells and their debris by scanning electron microscopy. Although we could not detect any living cells after 100 days, about 50% of the carbon remained in the soil after 224 days. The amount of label in the fatty acids indicated that microbial lipids were degraded faster than the bulk microbial biomass. Their labeling pattern showed that they were redistributed from E. coli to the microbial food web and from the living biomass to non-living soil organic matter. In contrast, the label in the total amino acids did not decrease significantly during incubation. Proteins are thus surprisingly stable in soil, but they also shifted from microbial biomass to non-living soil organic matter. The scanning electron micrographs showed only isolated intact microbial cells in our soil, but patches of organic material of unknown origin which are about 20 - 50 nm2 in size were quite abundant. Dying microbial cells therefore are a significant carbon source for the formation of refractory organic material, but the morphology of the cells changes during degradation, as cell structures cannot be found frequently in soils.

  13. Organic Matter Loading Affects Lodgepole Pine Seedling Growth

    NASA Astrophysics Data System (ADS)

    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.

  14. Analysis of organic refractory residues coming from the heating of cometary ice analogs: an insight in complex cometary chemistry

    NASA Astrophysics Data System (ADS)

    Danger, Grégoire; Abou Mrad, Ninette; Fresnau, Aurelien; Duvernay, Fabrice; Chiavassa, Thierry

    2015-04-01

    This contribution focuses on one aspect of our work, which relate to the analysis of refractory residues formed from UV irradiation and warming of astrophysical ice analogs, the RAHIIA project. The understanding of the formation of refractory residues, commonly called "Yellow Stuff" is an important step to establish what kind of organic matter could be available within interplanetary objects such as comets or asteroids. We present here the first results obtained by spectrometric analysis with high resolution mass spectroscopy (LT-Orbitrap) of these residues. These analyzes show that these residues are composed of thousands of molecules of high molecular weight (m / z> 4000), and present an average elemental composition H/C= 1.6, N/C= 0.4, O/C= 0.4 for an initial ice containing H2O:CH3OH:NH3 3:1:1. We further develop specific data representation in order to obtain information on the residue composition. These representations allow to define that three different groups of molecules are present in these residues, molecules bearing only CHN, CHO or CHNO atoms. These representations also give important information on the family composition of each molecular group. All these developments will be used for the comparison of various residues as well as for the development of more specific analytical methods such as UHPLC-MS or GC-MS. In conclusion, these results demonstrate that from only three simple molecules CH3OH, H2O and NH3, a complex chemistry occurs when these molecules are subjected to physical processes available in cometary environments.

  15. Organic matter of urban soils: A review

    NASA Astrophysics Data System (ADS)

    Vodyanitskii, Yu. N.

    2015-08-01

    Urban environment exerts an ambiguous effect on the organic pool of soils; it may decrease (as compared to the background values) in some parts of a city and increase in other parts. The organic matter accumulation in urban soils is promoted by the input of aerial organic pollutants; slowed down mineralization of plant residues under the influence of contamination; and increased productivity of the plants owing to elevated temperatures, high content of carbon dioxide in the air, and maintenance of green zones (sodding of vast areas in cities, application of peat, irrigation and drainage of soils.)

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

    USGS Publications Warehouse

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

    2015-01-01

    The U.S. Geological Survey (USGS), in cooperation with Clean Water Services, recently completed an investigation into the sources, transport, and fate of organic matter in the Fanno Creek watershed. The information provided by this investigation will help resource managers to implement strategies aimed at decreasing the excess supply of organic matter that contributes to low dissolved-oxygen levels in Fanno Creek and downstream in the Tualatin River during summer. This fact sheet summarizes the findings of the investigation.

  17. Organic matter and sandstone-type uranium deposits: a primer

    USGS Publications Warehouse

    Leventhal, Joel S.

    1979-01-01

    Organic material is intimately associated with sandstone-type uranium deposits in the western United States.. This report gives details of the types of organic matter and their possible role in producing a uranium deposit. These steps include mobilization of uranium from igneous rocks, transportation from the surface, concentration by organic matter, reduction by organic matter, and preservation of the uranium deposit.

  18. Subaerial weathering of sedimentary organic matter

    USGS Publications Warehouse

    Clayton, J.L.; Swetland, P.J.

    1978-01-01

    Small diameter core samples were taken from outcrops of the Permian Phosphoria Formation and the Cretaceous Pierre Shale of the Western United States to determine the effects of weathering on organic matter in shale outcrops. While the Pierre Shale core showed no evidence of weathering, the Phosphoria Formation showed significant reduction of overall organic content and pronounced changes in organic composition over the near-surface interval of the core. Total organic carbon is lower by as much as 60% over the upper 2 ft of the core. Chloroform-soluble organic matter and total hydrocarbon (C15+) concentrations are 50% lower over this same interval. The ratio of saturated to aromatic hydrocarbons decreases steadily with core depth over the upper 2.6 ft of the core. Aromatic hydrocarbons are enriched in the stable carbon-13 isotope by an average of 1.7%. over this same interval. Shallow core samples also show a loss of n-paraffins relative to branched/cyclic compounds in the saturated C15+ fraction. Although the extent of weathering is variable, certain characteristic effects are recognizable and can be applied to the interpretation of outcrop data in organic geochemical studies. ?? 1978.

  19. Isotopic analysis of cometary organic matter

    NASA Astrophysics Data System (ADS)

    Kerridge, J. F.

    1991-04-01

    Carbon isotope ratios have been measured for CN in the coma of Comet Halley and for several CHON particles emitted by Halley. Of these, only the CHON-particle data may be reasonably related to organic matter in the cometary nucleus, but the true range of (C-13)/(C-12) values in those particles is quite uncertain. The D/H ratio in H2O in the Halley coma resembles that in Titan/Uranus.

  20. Isotopic analysis of cometary organic matter

    NASA Technical Reports Server (NTRS)

    Kerridge, John F.

    1991-01-01

    Carbon isotope ratios have been measured for CN in the coma of Comet Halley and for several CHON particles emitted by Halley. Of these, only the CHON-particle data may be reasonably related to organic matter in the cometary nucleus, but the true range of (C-13)/(C-12) values in those particles is quite uncertain. The D/H ratio in H2O in the Halley coma resembles that in Titan/Uranus.

  1. Analysis of Organic matter from cloud particles

    NASA Astrophysics Data System (ADS)

    Bank, Shelton; Castillo, Raymond

    1987-03-01

    Organic matter collected from filtration of two separate cloud events was analysed by Fourier Transform Infrared Spectroscopy. Particles collected from different size filters were separated by color and each type of particle gave rise to a characteristic spectrum. The major constituents were identified as complex proteins and cellulose. Additionally, some degraded material (likely protein) and an unidentified orange-brown material were present. Finally some trace components were identified as wax, oil, silicon oil, polyvinyl chloride, calcium carbonate, clay, sand and polyethylene.

  2. Isolation and chemical characterization of dissolved and colloidal organic matter

    USGS Publications Warehouse

    Aiken, G.; Leenheer, J.

    1993-01-01

    Commonly used techniques for the concentration and isolation of organic matter from water, such as preparative chromatography, ultrafiltration and reverse osmosis, and the methods used to analyze the organic matter obtained by these methods are reviewed. The development of methods to obtain organic matter that is associated with fractions of the dissolved organic carbon other than humic substances, such as organic bases, hydrophilic organic acids and colloidal organic matter are discussed. Methods specifically used to study dissolved organic nitrogen and dissolved organic phosphorous are also discussed. -from Authors

  3. Simultaneous degradation of toxic refractory organic pesticide and bioelectricity generation using a soil microbial fuel cell.

    PubMed

    Cao, Xian; Song, Hai-liang; Yu, Chun-yan; Li, Xian-ning

    2015-01-01

    In this study, the soil microbial fuel cells (MFCs) were constructed in the topsoil contaminated with toxic refractory organic pesticide, hexachlorobenzene (HCB). The performance of electricity generation and HCB degradation in the soil-MFCs were investigated. The HCB degradation pathway was analyzed based on the determination of degradation products and intermediates. Experimental results showed that the HCB removal efficiencies in the three groups (soil MFCs group, open circuit control group and no adding anaerobic sludge blank group) were 71.15%, 52.49% and 38.92%, respectively. The highest detected power density was 77.5 mW/m(2) at the external resistance of 1000 Ω. HCB was degraded via the reductive dechlorination pathway in the soil MFC under anaerobic condition. The existence of the anode promoted electrogenic bacteria to provide more electrons to increase the metabolic reactions rates of anaerobic bacteria was the main way which could promote the removal efficiencies of HCB in soil MFC.

  4. Measuring Organic Matter with COSIMA on Board Rosetta

    NASA Astrophysics Data System (ADS)

    Briois, C.; Baklouti, D.; Bardyn, A.; Cottin, H.; Engrand, C.; Fischer, H.; Fray, N.; Godard, M.; Hilchenbach, M.; von Hoerner, H.; Höfner, H.; Hornung, K.; Kissel, J.; Langevin, Y.; Le Roy, L.; Lehto, H.; Lehto, K.; Orthous-Daunay, F. R.; Revillet, C.; Rynö, J.; Schulz, R.; Silen, J. V.; Siljeström, S.; Thirkell, L.

    2014-12-01

    Comets are believed to contain the most pristine material of our Solar System materials and therefore to be a key to understand the origin of the Solar System, and the origin of life. Remote sensing observations have led to the detection of more than twenty simple organic molecules (Bockelée-Morvan et al., 2004; Mumma and Charnley, 2011). Experiments on-board in-situ exploration missions Giotto and Vega and the recent Stardust sample return missions have shown that a significant fraction of the cometary grains consists of organic matter. Spectra showed that both the gaseous (Mitchell et al., 1992) and the solid phase (grains) (Kissel and Krueger, 1987) contained organic molecules with higher masses than those of the molecules detected by remote sensing techniques in the gaseous phase. Some of the grains analyzed in the atmosphere of comet 1P/Halley seem to be essentially made of a mixture of carbon, hydrogen, oxygen and nitrogen (CHON grains, Fomenkova, 1999). Rosetta is an unparalleled opportunity to make a real breakthrough into the nature of cometary matter, both in the gas and in the solid phase. The dust mass spectrometer COSIMA on Rosetta will analyze organic and inorganic phases in the dust. The organic phases may be refractory, but some organics may evaporate with time from the dust and lead to an extended source in the coma. Over the last years, we have prepared the cometary rendezvous by the analysis of various samples with the reference model of COSIMA. We will report on this calibration data set and on the first results of the in-situ analysis of cometary grains as captured, imaged and analyzed by COSIMA. References : Bockelée-Morvan, D., et al. 2004. (Eds.), Comets II. the University of Arizona Press, Tucson, USA, pp. 391-423 ; Fomenkova, M.N., 1999. Space Science Reviews 90, 109-114 ; Kissel, J., Krueger, F.R., 1987. Nature 326, 755-760 ; Mitchell, et al. 1992. Icarus 98, 125-133 ; Mumma, M.J., Charnley, S.B., 2011. Annual Review of Astronomy and

  5. Dissolved organic matter reduces algal accumulation of methylmercury

    USGS Publications Warehouse

    Luengen, Allison C.; Fisher, Nicholas S.; Bergamaschi, Brian A.

    2012-01-01

    Dissolved organic matter (DOM) significantly decreased accumulation of methylmercury (MeHg) by the diatom Cyclotella meneghiniana in laboratory experiments. Live diatom cells accumulated two to four times more MeHg than dead cells, indicating that accumulation may be partially an energy-requiring process. Methylmercury enrichment in diatoms relative to ambient water was measured by a volume concentration factor (VCF). Without added DOM, the maximum VCF was 32 x 104, and the average VCF (from 10 to 72 h) over all experiments was 12.6 x 104. At very low (1.5 mg/L) added DOM, VCFs dropped by approximately half. At very high (20 mg/L) added DOM, VCFs dropped 10-fold. Presumably, MeHg was bound to a variety of reduced sulfur sites on the DOM, making it unavailable for uptake. Diatoms accumulated significantly more MeHg when exposed to transphilic DOM extracts than hydrophobic ones. However, algal lysate, a labile type of DOM created by resuspending a marine diatom in freshwater, behaved similarly to a refractory DOM isolate from San Francisco Bay. Addition of 67 μM L-cysteine resulted in the largest drop in VCFs, to 0.28 x 104. Although the DOM composition influenced the availability of MeHg to some extent, total DOM concentration was the most important factor in determining algal bioaccumulation of MeHg.

  6. Abiotic Bromination of Soil Organic Matter.

    PubMed

    Leri, Alessandra C; Ravel, Bruce

    2015-11-17

    Biogeochemical transformations of plant-derived soil organic matter (SOM) involve complex abiotic and microbially mediated reactions. One such reaction is halogenation, which occurs naturally in the soil environment and has been associated with enzymatic activity of decomposer organisms. Building on a recent finding that naturally produced organobromine is ubiquitous in SOM, we hypothesized that inorganic bromide could be subject to abiotic oxidations resulting in bromination of SOM. Through lab-based degradation treatments of plant material and soil humus, we have shown that abiotic bromination of particulate organic matter occurs in the presence of a range of inorganic oxidants, including hydrogen peroxide and assorted forms of ferric iron, producing both aliphatic and aromatic forms of organobromine. Bromination of oak and pine litter is limited primarily by bromide concentration. Fresh plant material is more susceptible to bromination than decayed litter and soil humus, due to a labile pool of mainly aliphatic compounds that break down during early stages of SOM formation. As the first evidence of abiotic bromination of particulate SOM, this study identifies a mechanistic source of the natural organobromine in humic substances and the soil organic horizon. Formation of organobromine through oxidative treatments of plant material also provides insights into the relative stability of aromatic and aliphatic components of SOM.

  7. Soil organic matter composition affected by potato cropping managements

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Organic matter is a small but important soil component. As a heterogeneous mixture of geomolecules and biomolecules, soil organic matter (SOM) can be fractionated into distinct pools with different solubility and lability. Water extractable organic matter (WEOM) fraction is the most labile and mobil...

  8. The surface area of soil organic matter

    USGS Publications Warehouse

    Chiou, C.T.; Lee, J.-F.; Boyd, S.A.

    1990-01-01

    The previously reported surface area for soil organic matter (SOM) of 560-800 m2/g as determined by the ethylene glycol (EG) retention method was reexamined by the standard BET method based on nitrogen adsorption at liquid nitrogen temperature. Test samples consisted of two high organic content soils, a freeze-dried soil humic acid, and an oven-dried soil humic acid. The measured BET areas for these samples were less than 1 m2/g, except for the freeze-dried humic acid. The results suggest that surface adsorption of nonionic organic compounds by SOM is practically insignificant in comparison to uptake by partition. The discrepancy between the surface areas of SOM obtained by BET and EG methods was explained in terms of the 'free surface area' and the 'apparent surface area' associated with these measurements.The previously reported surface area for soil organic matter (SOM) of 560-800 m2/g as determined by the ethylene glycol (EG) retention method was reexamined by the standard BET method based on nitrogen adsorption at liquid nitrogen temperature. Test samples consisted of two high organic content soils, a freeze-dried soil humic acid, and an oven-dried soil humic acid. The measured BET areas for these samples were less than 1 m2/g, except for the freeze-dried humic acid. The results suggest that surface adsorption of nonionic organic compounds by SOM is practically insignificant in comparison to uptake by partition. The discrepancy between the surface areas of SOM obtained by BET and EG methods was explained in terms of the 'free surface area' and the 'apparent surface area' associated with these measurements.

  9. Organic geochemical analysis of sedimentary organic matter associated with uranium

    USGS Publications Warehouse

    Leventhal, J.S.; Daws, T.A.; Frye, J.S.

    1986-01-01

    Samples of sedimentary organic matter from several geologic environments and ages which are enriched in uranium (56 ppm to 12%) have been characterized. The three analytical techniqyes used to study the samples were Rock-Eval pyrolysis, pyrolysis-gas chromatography-mass spectrometry, and solid-state C-13 nuclear magnetic resonance (NMR) spectroscopy. In samples with low uranium content, the pyrolysis-gas chromatography products contain oxygenated functional groups (as hydroxyl) and molecules with both aliphatic and aromatic carbon atoms. These samples with low uranium content give measurable Rock-Eval hydrocarbon and organic-CO2 yields, and C-13 NMR values of > 30% aliphatic carbon. In contrast, uranium-rich samples have few hydrocarbon pyrolysis products, increased Rock-Eval organic-CO2 contents and > 70% aromatic carbon contents from C-13 NMR. The increase in aromaticity and decrease in hydrocarbon pyrolysis yield are related to the amount of uranium and the age of the uranium minerals, which correspond to the degree of radiation damage. The three analytical techniques give complementary results. Increase in Rock-Eval organic-CO2 yield correlates with uranium content for samples from the Grants uranium region. Calculations show that the amount of organic-CO2 corresponds to the quantity of uranium chemically reduced by the organic matter for the Grants uranium region samples. ?? 1986.

  10. Laboratory Investigations of Complex Refractory Organic Material Produced from Irradiation of Pluto Ice Analogs

    NASA Astrophysics Data System (ADS)

    Materese, Christopher K.; Cruikshank, Dale P.; Sandford, Scott A.; Imanaka, Hiroshi

    2014-11-01

    Much of Pluto’s surface consists of N2 ice with smaller amounts of CH4 and CO ices. Despite the low temperature 45K), chemistry can be driven in the surface ices by radiation processing such as cosmic ray bombardment. When cosmic rays strike the surface, much of their energy is dispersed in the form of secondary electrons, which in turn drive much of the resulting chemical reactions. Laboratory experiments designed to simulate the conditions on these icy bodies may provide insight into this chemistry. Significant progress has been made in the laboratory toward understanding the smaller, simple compounds produced in the solid phase by radiation processing of (N2, CH4, CO) ices (Bohn et al. 1994; Moore & Hudson 2003; Hodyss et al. 2011; Kim and Kaiser 2012). Recently Materese et al. (2014) used a variety of techniques to better characterize the refractory materials produced from the UV photo-irradiation of N2:CH4:CO ices. However, because Pluto’s atmosphere is optically thick to Lyman-α UV radiation it is important to re-examine the results using an alternate radiation source. Our latest work has consisted of the analysis of refractory materials produced from the electron bombardment of low-temperature N2-, CH4-, and CO-containing ices (100:1:1). The ice mixture was chosen to be analogous to the known surface ices on Pluto and the radiation source was chosen to mimic the secondary electrons produced by cosmic rays bombardment. The residues were studied using multiple chemical techniques including, infrared (IR) spectroscopy, X-ray absorption near-edge structure (XANES) spectroscopy, and gas chromatography coupled with mass spectrometry (GC-MS). The organic residues produced in these experiments can be seen as an analog for the refractory component of the surface of Pluto, and are compared with the residues previously obtained from UV photo-irradiation. UV and near-IR spectroscopy of the surfaces of Pluto and Charon during the encounter with NASA’s New Horizons

  11. Laboratory Investigations of the Complex Refractory Organic Material Produced from Irradiation of Pluto Ice Analogs

    NASA Technical Reports Server (NTRS)

    Materese, Christopher K.; Cruikshank, Dale P.; Sanford, Scott A.; Imanaka, Hiroshi

    2014-01-01

    Much of Pluto's surface consists of N2 ice with smaller amounts of CH4 and CO ices. Despite the low temperature (approximately 45K), chemistry can be driven in the surface ices by radiation processing such as cosmic ray bombardment. When cosmic rays strike the surface, much of their energy is dispersed in the form of secondary electrons, which in turn drive much of the resulting chemical reactions. Laboratory experiments designed to simulate the conditions on these icy bodies may provide insight into this chemistry. Significant progress has been made in the laboratory toward understanding the smaller, simple compounds produced in the solid phase by radiation processing of (N2, CH4, CO) ices (Bohn et al. 1994; Moore & Hudson 2003; Hodyss et al. 2011; Kim and Kaiser 2012). Recently Materese et al. (2014) used a variety of techniques to better characterize the refractory materials produced from the UV photo-irradiation of N2:CH4:CO ices. However, because Pluto's atmosphere is optically thick to Lyman-alpha UV radiation it is important to re-examine the results using an alternate radiation source. Our latest work has consisted of the analysis of refractory materials produced from the electron bombardment of low temperature N2(-), CH4(-), and CO(-)containing ices (100:1:1). The ice mixture was chosen to be analogous to the known surface ices on Pluto and the radiation source was chosen to mimic the secondary electrons produced by cosmic rays bombardment. The residues were studied using multiple chemical techniques including, infrared (IR) spectroscopy, X-ray absorption near-edge structure (XANES) spectroscopy, and gas chromatography coupled with mass spectrometry (GC-MS). The organic residues produced in these experiments can be seen as an analog for the refractory component of the surface of Pluto, and are compared with the residues previously obtained from UV photo-irradiation. UV and near- IR spectroscopy of the surfaces of Pluto and Charon during the encounter with

  12. Fluorescent organic matter in carbonaceous chondrites.

    PubMed

    Murae, T

    1999-01-01

    Fluorescent organic matter in carbonaceous chondrites was investigated using a microscope equipped with a fluorescence spectrophotometer. Fluorescent particles were observed in powdered CM2 carbonaceous chondrites (Y-74662, Y-7791198, and Murchison) without carbon enrichment by acid treatments. Although it was difficult to find fluorescent particles in powdered sample of C3 chondrites (ALH-77307, Y-791717, and Allende) without acid treatments, many fluorescent particles were observed after carbon enrichment by acid treatments. Fluorescence of coronene and shock-altered graphite were observed using the same microscope and the same conditions as those for carbonaceous chondrites.

  13. Mapping Soil Organic Matter with Hyperspectral Imaging

    NASA Astrophysics Data System (ADS)

    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

  14. The fate of airborne polycyclic organic matter.

    PubMed Central

    Nielsen, T; Ramdahl, T; Bjørseth, A

    1983-01-01

    Biological tests have shown that a significant part of the mutagenicity of organic extracts of collected airborne particulate matter is not due to polycyclic aromatic hydrocarbons (PAH). It is possible that part of these unknown compounds are transformation products of PAH. This survey focuses on the reaction of PAH in the atmosphere with other copollutants, such as nitrogen oxides, sulfur oxides, ozone and free radicals and their reaction products. Photochemically induced reactions of PAH are also included. The reactivity of particle-associated PAH is discussed in relation to the chemical composition and the physical properties of the carrier. Recommendations for future work are given. PMID:6825615

  15. Organic Matter in the Outer Solar System

    NASA Technical Reports Server (NTRS)

    Cruiskshank, Dale P.; DeVincenzi, Donald L. (Technical Monitor)

    2000-01-01

    Many solid bodies in the outer Solar System are covered with ices of various compositions, including water, carbon dioxide, methane, nitrogen, and other molecules that are solid at the low temperatures that prevail there. These ices have all been detected by remote sensing observations made with telescopes on Earth, or more recently, spacecraft in orbit (notably Galileo at Jupiter). The data also reveal other solid materials that could be minerals or complex carbon-bearing organic molecules. A study in progress using large ground-based telescopes to acquire infrared spectroscopic data, and laboratory results on the optical properties of complex organic matter, seeks to identify the non-icy materials on several satellites of Saturn, Uranus, and Neptune. The work on the satellites of Saturn is in part preparatory to the Cassini spacecraft investigation of the Saturn system, which will begin in 2004 and extend for four years.

  16. Land-use Effect on Stream Organic Matter Composition in Two Metropolitan Areas in USA

    NASA Astrophysics Data System (ADS)

    Duan, S.; Kaushal, S.; Amon, R. M.; Brinkmeyer, R.

    2011-12-01

    Urbanization is a form of land-use change that is increasing in coastal watersheds and may affect the quantity and quality of organic carbon delivered to streams and coastal ocean. Here, we examine the changes in optical and isotopic characteristics of organic matter in streams (Gwynns Fall and Buffalo Bayou) draining Baltimore and Houston Metropolitan Areas (USA), relative to nearby less affected forested watersheds. A summer longitudinal sampling in Gwynns Fall along a rural-urban gradient showed increases in dissolved organic carbon (DOC) and fluorescent protein to humic ratio but a decrease in specific UV absorption (SUVA). Parallel Factor modeling shows dominance of terrestrial component of DOC, and the ratio of an unknown component to the component of humic substance was high in urban watersheds and it was positively correlated impervious surface cover (an index of urbanization). Incubation experiments with leaves and stream algae suggest origin of decayed leaf leachate of this component. Conversely, DOM in Buffalo Bayou showed higher intensity of protein-like fluorescence, and the intensity increased longitudinal along a rural-urban gradient but decreased from low-flows to a flooding event. The difference in fluorescent organic matter composition between the two streams probably reflected different management of wastewater in watersheds. Surface sediment collected at sites of sub-watersheds of Gwynns Fall showed changes in particle size, elemental and isotopic composition with land use. Sediment incubations showed that higher temperature (due to urban heat island effect) enhanced loss of labile organic matter and release of refractory organic matter into stream water. Release of reactive soluble phosphorus, loss of nitrogen and reduction of sulfate also occurred at high incubating temperatures, along with mineralization of sediment organic matter. Bed sediment collected along Buffalo Bayou displayed a longitudinal decrease in N-15, probably reflecting the

  17. Soil organic matter mineralization in frozen soils

    NASA Astrophysics Data System (ADS)

    Harrysson Drotz, S.; Sparrman, T.; Schleucher, J.; Nilsson, M.; Öquist, M. G.

    2009-12-01

    Boreal forest soils are frozen for a large part of the year and soil organic matter mineralization during this period has been shown to significantly influence the C balance of boreal forest ecosystems. Mineralization proceeds through heterotrophic microbial activity, but the understanding of the environmental controls regulating soil organic matter mineralization under frozen conditions is poor. Through a series of investigations we have addressed this issue in order to elucidate to what extent a range of environmental factors control mineralization processes in frozen soils and also the microbial communities potential to oxidize organic substrates and grow under such conditions. The unfrozen water content in the frozen soils was shown to be an integral control on the temperature response of biogenic CO2 production across the freezing point of bulk soil water. We found that osmotic potential was an important contributor to the total water potential and, hence, the unfrozen water content of frozen soil. From being low and negligible in an unfrozen soil, the osmotic potential was found to contribute up to 70% of the total water potential in frozen soil, greatly influencing the volume of liquid water. The specific factors of how soil organic matter composition affected the unfrozen water content and CO2 production of frozen soil were studied by CP-MAS NMR. We concluded that abundance of aromatics and recalcitrant compounds showed a significant positive correlation with unfrozen water content and these were also the major soil organic fractions that similarly correlated with the microbial CO2 production of the frozen soils. Thus, the hierarchy of environmental factors controlling SOM mineralization changes as soils freeze and environmental controls elucidated from studies of unfrozen systems can not be added on frozen conditions. We have also investigated the potential activity of soil microbial communities under frozen conditions in order to elucidate temperature

  18. Stability of Ferrihydrite and Organic Matter in Ferrihydrite-Organic Matter Associations

    NASA Astrophysics Data System (ADS)

    Eusterhues, K.; Totsche, K. U.

    2015-12-01

    Iron oxides can bind particularly large amounts of organic matter (OM) and seem to be an important control on OM storage in many soils. To better understand the interactions between Fe oxides and OM, we produced ferrihydrite-OM associations by adsorption and coprecipitation in laboratory experiments. Because ferrihydrites are often formed in OM-rich solutions, we assume that coprecipitation is a common process in nature. In contrast to adsorption on pre-existing ferrihydrite surfaces, coprecipitation involves adsorption, occlusion (physical entrapment of OM), formation of Fe-OM complexes, and poisoning of ferrihydrite growth. The reactivity of coprecipitates may therefore differ from ferriydrites with adsorbed OM. Incubation experiments with an inoculum extracted from a Podzol forest-floor were carried out to quantify the mineralization of the adsorbed and coprecipitated organic matter. These experiments showed that the association with ferrihydrite stabilized the associated organic matter, but that differences in the degradability of adsorbed and coprecipitated organic matter were small. We therefore conclude that coprecipitation does not lead to a significant formation of microbial inaccessible organic matter domains. Microbial reduction experiments were performed using Geobacter bremensis. We observed that increasing amounts of associated OM led to decreasing initial reaction rates and a decreasing degree of dissolution. Reduction of coprecipitated ferrihydrites was faster than reduction of ferrihydrites with adsorbed OM. Our data demonstrate that the association with ferrihydrite can effectively stabilize labile polysaccharides. Vice versa, these polysaccharides may protect ferrihydrite from reduction by Geobacter-like bacteria. However, a challenge for future studies will be to link formation and degradation of mineral-organic associations to natural porous systems, that is, to the complex interplay of mass transport and microbial distribution in the

  19. Detection of organic matter in interstellar grains.

    PubMed

    Pendleton, Y J

    1997-06-01

    Star formation and the subsequent evolution of planetary systems occurs in dense molecular clouds, which are comprised, in part, of interstellar dust grains gathered from the diffuse interstellar medium (DISM). Radio observations of the interstellar medium reveal the presence of organic molecules in the gas phase and infrared observational studies provide details concerning the solid-state features in dust grains. In particular, a series of absorption bands have been observed near 3.4 microns (approximately 2940 cm-1) towards bright infrared objects which are seen through large column densities of interstellar dust. Comparisons of organic residues, produced under a variety of laboratory conditions, to the diffuse interstellar medium observations have shown that aliphatic hydrocarbon grains are responsible for the spectral absorption features observed near 3.4 microns (approximately 2940 cm-1). These hydrocarbons appear to carry the -CH2- and -CH3 functional groups in the abundance ratio CH2/CH3 approximately 2.5, and the amount of carbon tied up in this component is greater than 4% of the cosmic carbon available. On a galactic scale, the strength of the 3.4 microns band does not scale linearly with visual extinction, but instead increases more rapidly for objects near the Galactic Center. A similar trend is noted in the strength of the Si-O absorption band near 9.7 microns. The similar behavior of the C-H and Si-O stretching bands suggests that these two components may be coupled, perhaps in the form of grains with silicate cores and refractory organic mantles. The ubiquity of the hydrocarbon features seen in the near infrared near 3.4 microns throughout out Galaxy and in other galaxies demonstrates the widespread availability of such material for incorporation into the many newly forming planetary systems. The similarity of the 3.4 microns features in any organic material with aliphatic hydrocarbons underscores the need for complete astronomical observational

  20. Influence of land use on soil organic matter

    NASA Astrophysics Data System (ADS)

    Rogeon, H.; Lemée, L.; Chabbi, A.; Ambles, A.

    2009-04-01

    Soil organic matter (SOM) is actually of great environmental interest as the amount of organic matter stored in soils represents one of the largest reservoirs of organic carbon on the global scale [1]. Indeed, soil carbon storage capacity represents 1500 to 2000 Gt for the first meter depth, which is twice the concentration of atmospheric CO2 [2]. Furthermore, human activities, such as deforestation (which represents a flux of 1.3 Gt C/year), contribute to the increase in atmospheric CO2 concentration for about one percent a year [3]. Therefore, carbon dioxide sequestration in plant and carbon storage in soil and biomass could be considered as a complementary solution against climate change. The stock of carbon in soils is greatly influenced by land use (ca 70 Gt for a forest soil or a grassland against 40 Gt for an arable land). Furthermore the molecular composition of SOM should be also influenced by vegetation. In this context, four horizons taken between 0-120 cm from the same profile of a soil under grassland and forest located in the vicinity of Poitiers (INRA Lusignan, ORE Prairie) were compared. For the surface horizon, the study is improved with the results from the cultivated soil from INRA Versailles. Soil organic matter was characterized using IR spectroscopy, elemental analysis and thermal analysis. Granulometric fractionation into sand (50-2000 μm), silt (2-50 μm) and clay (<2 μm) was conducted. The organic matter associated with the mineral fractions was thus characterized using thermochemolysis coupled with gas chromatography and mass spectrometry (Py-GC/MS). The total lipidic fractions were extracted with CH2Cl2/MeOH using an accelerated solvent extraction (ASE). In the three soils, lipids are concentrated into the superficial horizon (0-30 cm) which indicates a low mobilisation. Lipids from the superficial horizon are more abundant for the arable soil (1010 ppm) than for the two other (400 ppm). Lipids from the forest and the grassland were

  1. Adsorption into mineral mesopores as a stabilization mechanism for organic matter on aluminosilicates

    SciTech Connect

    Mayer, L.M. . Dept. of Oceanography)

    1992-01-01

    Measurements of mineral specific surface area and total organic carbon (TOC) indicate that many marine shelf and estuarine sediments, and aluminosilicate soils, have a TOC content equivalent to a monolayer of organic matter covering all mineral surfaces. Density separations of discrete organic particulates from mineral-associated OC are consistent with a primarily adsorbed nature foremost of TOC. Nitrogen gas adsorption data also suggest extensive organic coatings on the mineral grains. Downcore analyses indicate that sediments with TOC starting in excess of monolayer-equivalent (ME) levels decay with core depth to the ME level and then markedly slow their OC loss rate--i.e., the ME level determines the refractory background concentration of TOC. Pore size distributions of marine sediments, determined by nitrogen adsorption or mercury porosimetry, indicate that most surface area of minerals is to be found in pores of < 10 nm diameter. These observations lead to the hypothesis that organic matter is stabilized on aluminosilicate minerals by adsorption into pores too small to allow entry or functioning of the hydrolytic enzymes responsible for OC degradation. This hypothesis is consistent with, but does not require, humification reactions as necessary for OC stabilization. The ME levels of TOC found in continental platform aluminosilicates hence represent a cap on the amount of organic matter that can be protected in this manner and thus attain a residence time of > 1,000 y. Stabilization of higher levels of TOC, as in acid soils or anoxic sediments, presumably results from protection by different mechanisms.

  2. Turnover time of fluorescent dissolved organic matter in the dark global ocean.

    PubMed

    Catalá, Teresa S; Reche, Isabel; Fuentes-Lema, Antonio; Romera-Castillo, Cristina; Nieto-Cid, Mar; Ortega-Retuerta, Eva; Calvo, Eva; Álvarez, Marta; Marrasé, Cèlia; Stedmon, Colin A; Álvarez-Salgado, X Antón

    2015-01-29

    Marine dissolved organic matter (DOM) is one of the largest reservoirs of reduced carbon on Earth. In the dark ocean (>200 m), most of this carbon is refractory DOM. This refractory DOM, largely produced during microbial mineralization of organic matter, includes humic-like substances generated in situ and detectable by fluorescence spectroscopy. Here we show two ubiquitous humic-like fluorophores with turnover times of 435±41 and 610±55 years, which persist significantly longer than the ~350 years that the dark global ocean takes to renew. In parallel, decay of a tyrosine-like fluorophore with a turnover time of 379±103 years is also detected. We propose the use of DOM fluorescence to study the cycling of resistant DOM that is preserved at centennial timescales and could represent a mechanism of carbon sequestration (humic-like fraction) and the decaying DOM injected into the dark global ocean, where it decreases at centennial timescales (tyrosine-like fraction).

  3. Turnover time of fluorescent dissolved organic matter in the dark global ocean.

    PubMed

    Catalá, Teresa S; Reche, Isabel; Fuentes-Lema, Antonio; Romera-Castillo, Cristina; Nieto-Cid, Mar; Ortega-Retuerta, Eva; Calvo, Eva; Álvarez, Marta; Marrasé, Cèlia; Stedmon, Colin A; Álvarez-Salgado, X Antón

    2015-01-01

    Marine dissolved organic matter (DOM) is one of the largest reservoirs of reduced carbon on Earth. In the dark ocean (>200 m), most of this carbon is refractory DOM. This refractory DOM, largely produced during microbial mineralization of organic matter, includes humic-like substances generated in situ and detectable by fluorescence spectroscopy. Here we show two ubiquitous humic-like fluorophores with turnover times of 435±41 and 610±55 years, which persist significantly longer than the ~350 years that the dark global ocean takes to renew. In parallel, decay of a tyrosine-like fluorophore with a turnover time of 379±103 years is also detected. We propose the use of DOM fluorescence to study the cycling of resistant DOM that is preserved at centennial timescales and could represent a mechanism of carbon sequestration (humic-like fraction) and the decaying DOM injected into the dark global ocean, where it decreases at centennial timescales (tyrosine-like fraction). PMID:25631682

  4. Bacterial and organic matter distribution in the sediments of the Thracian Sea (NE Aegean Sea)

    NASA Astrophysics Data System (ADS)

    Polymenakou, Paraskevi N.; Fragkioudaki, Glykeria; Tselepides, Anastasios

    2007-10-01

    Recently, black carbon has been introduced as the form of carbon that may be separated from the biologically mediated carbon cycle thereby representing the non-bioavailable fraction of the estimated organic carbon. It has been speculated that the bioavailability of organic matter may be a limiting factor for the presence of active bacteria within the sediments. In order to address this question, marine sediments were collected from the Thracian Sea (Eastern Mediterranean), a complex system impacted by riverine inputs and Black Sea water masses. In addition to counts of total bacteria, we estimated the fraction of active bacteria by using a destaining step to the DAPI staining method. Black carbon was also estimated following the thermal oxidation method in order to determine the fraction of the refractory organic matter. The fraction of black carbon to total organic carbon varied from 16% to 53% indicating that black carbon constitutes a significant pool of sedimentary organic carbon in the Thracian sea. A fraction ranging from 18% to 97% was scored as nucleoid containing cells. We did not record any significant differences in the fraction of nucleoid-containing bacteria among sediment depths ( P<0.05) indicating that there was no accumulation of dead bacterial cells with depth. The same was observed for the fraction of black carbon and bioavailable organic carbon with sediment depth ( P<0.05) indicating that benthic consumers are not the key regulators of the organic matter pool in these sediments but have a minor effect. A possible reason for these observations and for the uncoupling between the active bacterial fraction and the bioavailability of organic matter could be (i) the presence of refractory components in the estimated bioavailable organic matter and (ii) the hydrological and geological complexity of the study area. The North Aegean marginal slopes are highly unstable experiencing frequent seismic events. These events are capable of inducing sediment

  5. Removal of refractory organics in nanofiltration concentrates of municipal solid waste leachate treatment plants by combined Fenton oxidative-coagulation with photo--Fenton processes.

    PubMed

    Li, Jiuyi; Zhao, Lei; Qin, Lele; Tian, Xiujun; Wang, Aimin; Zhou, Yanmei; Meng, Liao; Chen, Yong

    2016-03-01

    Removal of the refractory organic matters in leachate brines generated from nanofiltration unit in two full-scale municipal solid waste landfill leachate treatment plants was investigated by Fenton oxidative-coagulation and ultraviolet photo - Fenton processes in this study. Fenton oxidative-coagulation was performed under the condition of an initial pH of 5.0 and low H2O2/Fe(2+) ratios. After precipitate separation, the remaining organic constituents were further oxidized by photo - Fenton process. For both leachate brines with varying pollution strength, more than 90% COD and TOC reductions were achieved at H2O2/Fe(2+) dosages of 35 mM/8 mM and 90 mM/10 mM, respectively. The effluent COD ranged 120-160 mg/L under the optimal operating conditions, and the biodegradability was increased significantly. Fenton oxidative-coagulation was demonstrated to contribute nearly 70% overall removal of organic matters. In the combined processes, the efficiency of hydrogen peroxide varied from 216 to 228%, which may significantly reduce the operating cost of conventional Fenton method. Six phthalic acid esters and thirteen polycyclic aromatic hydrocarbons were found in leachate brines, and, on the average, around 80% phthalic acid esters and 90% polycyclic aromatic hydrocarbons were removed by the combined treatments.

  6. Removal of refractory organics in nanofiltration concentrates of municipal solid waste leachate treatment plants by combined Fenton oxidative-coagulation with photo--Fenton processes.

    PubMed

    Li, Jiuyi; Zhao, Lei; Qin, Lele; Tian, Xiujun; Wang, Aimin; Zhou, Yanmei; Meng, Liao; Chen, Yong

    2016-03-01

    Removal of the refractory organic matters in leachate brines generated from nanofiltration unit in two full-scale municipal solid waste landfill leachate treatment plants was investigated by Fenton oxidative-coagulation and ultraviolet photo - Fenton processes in this study. Fenton oxidative-coagulation was performed under the condition of an initial pH of 5.0 and low H2O2/Fe(2+) ratios. After precipitate separation, the remaining organic constituents were further oxidized by photo - Fenton process. For both leachate brines with varying pollution strength, more than 90% COD and TOC reductions were achieved at H2O2/Fe(2+) dosages of 35 mM/8 mM and 90 mM/10 mM, respectively. The effluent COD ranged 120-160 mg/L under the optimal operating conditions, and the biodegradability was increased significantly. Fenton oxidative-coagulation was demonstrated to contribute nearly 70% overall removal of organic matters. In the combined processes, the efficiency of hydrogen peroxide varied from 216 to 228%, which may significantly reduce the operating cost of conventional Fenton method. Six phthalic acid esters and thirteen polycyclic aromatic hydrocarbons were found in leachate brines, and, on the average, around 80% phthalic acid esters and 90% polycyclic aromatic hydrocarbons were removed by the combined treatments. PMID:26741550

  7. Origin of organic matter in the protosolar nebula and in comets

    NASA Technical Reports Server (NTRS)

    Greenberg, J. M.; Shalabiea, O. M.; Mendoza-Gomez, C. X.; Schutte, W.; Gerakines, P. A.

    1994-01-01

    Comet organics are traced to their origin in interstellar space. Possible sources of comet organics from solar nebula chemistry are briefly discussed. The infrared spectra of interstellar dust are compared with spectra of solar (space) irradiated laboratory organic residues and with meteorites. The spectra compare very favorably. The atomic composition of first generation laboratory organic residues compares favorably with that of comet Halley organics if divided into approrpriate 'volatile' (less refreactory) and 'refractory' (more refractory) complex organics.

  8. Soil Organic Matter and Management of Plant-Parasitic Nematodes

    PubMed Central

    Widmer, T. L.; Mitkowski, N. A.; Abawi, G. S.

    2002-01-01

    Organic matter and its replenishment has become a major component of soil health management programs. Many of the soil's physical, chemical, and biological properties are a function of organic matter content and quality. Adding organic matter to soil influences diverse and important biological activities. The diversity and number of free-living and plant-parasitic nematodes are altered by rotational crops, cover crops, green manures, and other sources of organic matter. Soil management programs should include the use of the proper organic materials to improve soil chemical, physical, and biological parameters and to suppress plant-parasitic nematodes and soilborne pathogens. It is critical to monitor the effects of organic matter additions on activities of major and minor plant-parasitic nematodes in the production system. This paper presents a general review of information in the literature on the effects of crop rotation, cover crops, and green manures on nematodes and their damage to economic crops. PMID:19265946

  9. Sensitivity of soil organic matter in anthropogenically disturbed organic soils

    NASA Astrophysics Data System (ADS)

    Säurich, Annelie; Tiemeyer, Bärbel; Bechtold, Michel; Don, Axel; Freibauer, Annette

    2016-04-01

    Drained peatlands are hotspots of carbon dioxide (CO2) emissions from agriculture. However, the variability of CO2 emissions increases with disturbance, and little is known on the soil properties causing differences between seemingly similar sites. Furthermore the driving factors for carbon cycling are well studied for both genuine peat and mineral soil, but there is a lack of information concerning soils at the boundary between organic and mineral soils. Examples for such soils are both soils naturally relatively high in soil organic matter (SOM) such as Humic Gleysols and former peat soils with a relative low SOM content due to intensive mineralization or mixing with underlying or applied mineral soil. The study aims to identify drivers for the sensitivity of soil organic matter and therefore for respiration rates of anthropogenically disturbed organic soils, especially those near the boundary to mineral soils. Furthermore, we would like to answer the question whether there are any critical thresholds of soil organic carbon (SOC) concentrations beyond which the carbon-specific respiration rates change. The German agricultural soil inventory samples all agricultural soils in Germany in an 8x8 km² grid following standardized protocols. From this data and sample base, we selected 120 different soil samples from more than 80 sites. As reference sites, three anthropogenically undisturbed peatlands were sampled as well. We chose samples from the soil inventory a) 72 g kg-1 SOC and b) representing the whole range of basic soil properties: SOC (72 to 568 g kg-1), total nitrogen (2 to 29 g kg-1), C-N-ratio (10 to 80) bulk density (0.06 to 1.41 g/cm³), pH (2.5 to 7.4), sand (0 to 95 %) and clay (2 to 70 %) content (only determined for samples with less than 190 g kg-1 SOC) as well as the botanical origin of the peat (if determinable). Additionally, iron oxides were determined for all samples. All samples were sieved (2 mm) and incubated at standardized water content and

  10. Spectrophotometric discrimination of river dissolved organic matter

    NASA Astrophysics Data System (ADS)

    Baker, Andy

    2002-11-01

    There is a need to be able to differentiate the dissolved organic matter (DOM) fraction in river waters. Research in the 1970s and 1980s has attempted to utilize both absorbance and fluorescence to distinguish between DOM fractions in river waters, but both were limited by the available technology. Total organic carbon content has, therefore, been widely used as a standard method of measuring DOM concentration, although it has little power to differentiate DOM fractions. Recent advances in fluorescence spectrophotometry enable rapid and optically precise analysis of DOM. Here, we show how a combination of both fluorescence and absorbance can be used to discriminate statistically between spatial variations of DOM in tributaries in a small catchment of the Ouseburn, NE England. The results of the discriminant analysis suggest that about 70% of the samples can be correctly classified to its tributary. Discriminant function 1 explains 60·8% of the variance in the data and the fulvic-like fluorescence intensity has the largest absolute correlation within this function; discriminant function 2 explains a further 21·5% of the variance and the fulvic-like fluorescence emission wavelength has the largest absolute correlation within this function. The discriminant analysis does not correctly classify all tributaries every time, and successfully discriminates between the different tributaries 70% of the time. Occasions when the tributary waters are less well discriminated are due to either episodic pollution events (at two sites) or due to tributaries that have strong seasonal trends in spectrophotometric parameters, which allows the sites to be misclassified. Results suggest that spectrophotometric techniques have considerable potential in the discrimination of DOM in rivers.

  11. The evolution of organic matter in space.

    PubMed

    Ehrenfreund, Pascale; Spaans, Marco; Holm, Nils G

    2011-02-13

    Carbon, and molecules made from it, have already been observed in the early Universe. During cosmic time, many galaxies undergo intense periods of star formation, during which heavy elements like carbon, oxygen, nitrogen, silicon and iron are produced. Also, many complex molecules, from carbon monoxide to polycyclic aromatic hydrocarbons, are detected in these systems, like they are for our own Galaxy. Interstellar molecular clouds and circumstellar envelopes are factories of complex molecular synthesis. A surprisingly high number of molecules that are used in contemporary biochemistry on the Earth are found in the interstellar medium, planetary atmospheres and surfaces, comets, asteroids and meteorites and interplanetary dust particles. Large quantities of extra-terrestrial material were delivered via comets and asteroids to young planetary surfaces during the heavy bombardment phase. Monitoring the formation and evolution of organic matter in space is crucial in order to determine the prebiotic reservoirs available to the early Earth. It is equally important to reveal abiotic routes to prebiotic molecules in the Earth environments. Materials from both carbon sources (extra-terrestrial and endogenous) may have contributed to biochemical pathways on the Earth leading to life's origin. The research avenues discussed also guide us to extend our knowledge to other habitable worlds.

  12. Silicate core-organic refractory mantle particles as interstellar dust and as aggregated in comets and stellar disks.

    PubMed

    Greenberg, J M; Li, A

    1997-01-01

    The principal observational properties of silicate core-organic refractory mantle interstellar dust grains in the infrared at 3.4 microns and at 10 microns and 20 microns are discussed in terms of the cyclic evolution of particles forming in stellar atmospheres and undergoing subsequent accretion, photoprocessing and destruction (erosion). Laboratory plus space emulation of the photoprocessing of laboratory analog ices and refractories are discussed. The aggregated interstellar dust model of comets is summarized. The same properties required to explain the temperature and infrared properties of comet coma dust are shown to be needed to account for the infrared silicate and continuum emission of the beta Pictoris disk as produced by a cloud of comets orbiting the star.

  13. THE REINCARNATION OF INTERSTELLAR DUST: THE IMPORTANCE OF ORGANIC REFRACTORY MATERIAL IN INFRARED SPECTRA OF COMETARY COMAE AND CIRCUMSTELLAR DISKS

    SciTech Connect

    Kimura, Hiroshi

    2013-09-20

    We consider the reincarnation of interstellar dust to be reborn in protoplanetary disks as aggregates consisting of submicron-sized grains with a crystalline or amorphous silicate core and an organic-rich carbonaceous mantle. We find that infrared spectra of reincarnated interstellar dust reproduce emission peaks at correct wavelengths where the peaks were observed in cometary comae, debris disks, and protoplanetary disks if the volume fraction of organic refractory meets the constraints on elemental abundances. We discuss what we can learn from the infrared spectra of reincarnated interstellar dust in cometary comae and circumstellar disks.

  14. Influence of sediment-organic matter quality on growth and polychlorobiphenyl bioavailability in Echinodermata (Amphiura filiformis)

    SciTech Connect

    Gunnarsson, J.S.; Granberg, M.E.; Nilsson, H.C.; Rosenberg, R.; Hellman, B.

    1999-07-01

    Sediment total organic carbon (TOC) content is considered to be a primary food source for benthic invertebrates and a major factor influencing the partitioning and bioavailability of sediment-associated organic contaminants. Most studies report that both toxicity and uptake of sediment-associated contaminants by benthic organisms are inversely proportional to sediment TOC content. The aim of this study was to determine the importance of the TOC quality for the bioavailability of sediment-associated organic contaminants and the growth of benthic macrofauna. The common infaunal brittle star Amphiura filiformis was exposed to a base sediment covered by a {sup 14}C-polychlorobipenyl (3,3{prime}4,4{prime}-{sup 14}C-tetrachlorobiphenyl (TCB)) contaminated top layer (0--2 cm), enriched to the same TOC content with 31 g TOC/m{sup 2} of different quality and origin. The following carbon sources, ranging from labile to refractory, were used: (1) green macroalga (Ulva lactuca), (2) brown macroalga (Ascophyllum nodosum), (3) eelgrass (Zostera Marina), (4) phytoplankton (Ceratium spp.), and (5) lignins of terrestrial origin. Characterization of the organic matter quality was accomplished by measuring the content of amino acids, lipids, C, N, and polyphenolic compounds. The reactivity of the sedimentary organic matter was assessed by means of respiration and dissolved inorganic nitrogen flux measurements. The experiment was carried out in 1-L glass jars, each containing four brittle stars and the contaminated and enriched sediment. The jars were circulated in a flow-through mode with filtered seawater. Somatic growth (regeneration of a precut arm) and bioaccumulation of {sup 14}C-TCB were measured at 10 sampling occasions during 48 d of exposure. Growth rates, TCB uptake rates, and steady-state concentrations differed significantly between treatments and were correlated to the qualities of the organic substrates. The greatest TCB accumulation and growth were observed in

  15. Complexation of trace metals by adsorbed natural organic matter

    USGS Publications Warehouse

    Davis, J.A.

    1984-01-01

    The adsorption behavior and solution speciation of Cu(II) and Cd(II) were studied in model systems containing colloidal alumina particles and dissolved natural organic matter. At equilibrium a significant fraction of the alumina surface was covered by adsorbed organic matter. Cu(II) was partitioned primarily between the surface-bound organic matter and dissolved Cu-organic complexes in the aqueous phase. Complexation of Cu2+ with the functional groups of adsorbed organic matter was stronger than complexation with uncovered alumina surface hydroxyls. It is shown that the complexation of Cu(II) by adsorbed organic matter can be described by an apparent stability constant approximately equal to the value found for solution phase equilibria. In contrast, Cd(II) adsorption was not significantly affected by the presence of organic matter at the surface, due to weak complex formation with the organic ligands. The results demonstrate that general models of trace element partitioning in natural waters must consider the presence of adsorbed organic matter. ?? 1984.

  16. Subcritical water extraction of organic matter from sedimentary rocks.

    PubMed

    Luong, Duy; Sephton, Mark A; Watson, Jonathan S

    2015-06-16

    Subcritical water extraction of organic matter containing sedimentary rocks at 300°C and 1500 psi produces extracts comparable to conventional solvent extraction. Subcritical water extraction of previously solvent extracted samples confirms that high molecular weight organic matter (kerogen) degradation is not occurring and that only low molecular weight organic matter (free compounds) are being accessed in analogy to solvent extraction procedures. The sedimentary rocks chosen for extraction span the classic geochemical organic matter types. A type I organic matter-containing sedimentary rock produces n-alkanes and isoprenoidal hydrocarbons at 300°C and 1500 psi that indicate an algal source for the organic matter. Extraction of a rock containing type II organic matter at the same temperature and pressure produces aliphatic hydrocarbons but also aromatic compounds reflecting the increased contributions from terrestrial organic matter in this sample. A type III organic matter-containing sample produces a range of non-polar and polar compounds including polycyclic aromatic hydrocarbons and oxygenated aromatic compounds at 300°C and 1500 psi reflecting a dominantly terrestrial origin for the organic materials. Although extraction at 300°C and 1500 psi produces extracts that are comparable to solvent extraction, lower temperature steps display differences related to organic solubility. The type I organic matter produces no products below 300°C and 1500 psi, reflecting its dominantly aliphatic character, while type II and type III organic matter contribute some polar components to the lower temperature steps, reflecting the chemical heterogeneity of their organic inventory. The separation of polar and non-polar organic compounds by using different temperatures provides the potential for selective extraction that may obviate the need for subsequent preparative chromatography steps. Our results indicate that subcritical water extraction can act as a suitable

  17. Extraterrestrial Organic Matter and the Detection of Life

    NASA Astrophysics Data System (ADS)

    Sephton, Mark A.; Botta, Oliver

    A fundamental goal of a number of forthcoming space missions is the detection and characterization of organic matter on planetary surfaces. Successful interpretation of data generated by in situ experiments will require discrimination between abiogenic and biogenic organic compounds. Carbon-rich meteorites provide scientists with examples of authentic extraterrestrial organic matter generated in the absence of life. Outcomes of meteorite studies include clues to protocols that will enable the unequivocal identification of organic matter derived from life. In this chapter we summarize the diagnostic abiogenic features of key compound classes involved in life detection and discuss their implications for analytical instruments destined to fly on future spacecraft missions.

  18. Extraterrestrial Organic Matter and the Detection of Life

    NASA Astrophysics Data System (ADS)

    Sephton, Mark A.; Botta, Oliver

    2008-03-01

    A fundamental goal of a number of forthcoming space missions is the detection and characterization of organic matter on planetary surfaces. Successful interpretation of data generated by in situ experiments will require discrimination between abiogenic and biogenic organic compounds. Carbon-rich meteorites provide scientists with examples of authentic extraterrestrial organic matter generated in the absence of life. Outcomes of meteorite studies include clues to protocols that will enable the unequivocal identification of organic matter derived from life. In this chapter we summarize the diagnostic abiogenic features of key compound classes involved in life detection and discuss their implications for analytical instruments destined to fly on future spacecraft missions.

  19. Subcritical water extraction of organic matter from sedimentary rocks.

    PubMed

    Luong, Duy; Sephton, Mark A; Watson, Jonathan S

    2015-06-16

    Subcritical water extraction of organic matter containing sedimentary rocks at 300°C and 1500 psi produces extracts comparable to conventional solvent extraction. Subcritical water extraction of previously solvent extracted samples confirms that high molecular weight organic matter (kerogen) degradation is not occurring and that only low molecular weight organic matter (free compounds) are being accessed in analogy to solvent extraction procedures. The sedimentary rocks chosen for extraction span the classic geochemical organic matter types. A type I organic matter-containing sedimentary rock produces n-alkanes and isoprenoidal hydrocarbons at 300°C and 1500 psi that indicate an algal source for the organic matter. Extraction of a rock containing type II organic matter at the same temperature and pressure produces aliphatic hydrocarbons but also aromatic compounds reflecting the increased contributions from terrestrial organic matter in this sample. A type III organic matter-containing sample produces a range of non-polar and polar compounds including polycyclic aromatic hydrocarbons and oxygenated aromatic compounds at 300°C and 1500 psi reflecting a dominantly terrestrial origin for the organic materials. Although extraction at 300°C and 1500 psi produces extracts that are comparable to solvent extraction, lower temperature steps display differences related to organic solubility. The type I organic matter produces no products below 300°C and 1500 psi, reflecting its dominantly aliphatic character, while type II and type III organic matter contribute some polar components to the lower temperature steps, reflecting the chemical heterogeneity of their organic inventory. The separation of polar and non-polar organic compounds by using different temperatures provides the potential for selective extraction that may obviate the need for subsequent preparative chromatography steps. Our results indicate that subcritical water extraction can act as a suitable

  20. Dissolved Organic Matter and Emerging Contaminants in Urban Stream Ecosystems

    NASA Astrophysics Data System (ADS)

    Kaushal, S. S.; Findlay, S.; Groffman, P.; Belt, K.; Delaney, K.; Sides, A.; Walbridge, M.; Mayer, P.

    2009-05-01

    We investigated the effects of urbanization on the sources, bioavailability and forms of natural and anthropogenic organic matter found in streams located in Maryland, U.S.A. We found that the abundance, biaoavailability, and enzymatic breakdown of dissolved organic carbon (DOC), dissolved organic nitrogen (DON), and dissolved organic phosphorus (DOP) increased in streams with increasing watershed urbanization suggesting that organic nutrients may represent a growing form of nutrient loading to coastal waters associated with land use change. Organic carbon, nitrogen, and phosphorus in urban streams were elevated several-fold compared to forest and agricultural streams. Enzymatic activities of stream microbes in organic matter decomposition were also significantly altered across watershed land use. Chemical characterization suggested that organic matter in urban streams originated from a variety of sources including terrestrial, sewage, and in-stream transformation. In addition, a characterization of emerging organic contaminants (polyaromatic cyclic hydrocarbons, organochlorine pesticides, and polybrominated diphenyl ether flame retardents), showed that organic contaminants and dissolved organic matter increase with watershed urbanization and fluctuate substantially with changing climatic conditions. Elucidating the emerging influence of urbanization on sources, transport, and in-stream transformation of organic nutrients and contaminants will be critical in unraveling the changing role of organic matter in urban degraded and restored stream ecosystems.

  1. Changes in River Organic Matter Through Time.

    NASA Astrophysics Data System (ADS)

    Hudson, N.; Baker, A.; Ward, D.

    2006-12-01

    fluorescence, as an increase in pH was also observed in these samples. This work illustrates the dynamic character of river organic matter within a timescale and under conditions that are representative of the natural system.

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

    PubMed

    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.

  3. P/Wirtanen thermal evolution: effects due to the presence of an organic component in the refractory material

    NASA Astrophysics Data System (ADS)

    Capria, M. T.; Coradini, A.; De Sanctis, M. C.; Blecka, M. I.

    2001-08-01

    In-situ experiments on cometary dust on board GIOTTO and VEGA missions demonstrated that in comet P/Halley's refractory component it is possible to evidentiate a refractory organic phase, the so called CHON, and a Mg-rich silicate phase. The two phases were interspersed in the individual grains. Each of these phases has different average physical properties. Laboratory experiments demonstrated that the characteristics of a crust mainly composed of silicatic particles would be different from that of a crust composed by silicatic and organic particles: thermal conductivities, for example, differ by orders of magnitude. In this paper we want to show how the simulation, in our numerical model of cometary nucleus thermal evolution, of two different dust distributions with different and independent physical properties gives us a much better modeling of the complexity of real phenomena. We attributed to one of these distributions the characteristics, taken mainly from laboratory experiments, of silicatic/organic material, and to the other one the characteristics of purely silicatic material. We applied the model to improve our simulation of comet P/Wirtanen, the target of Rosetta mission. Local temperature and evolution of the crust are different depending on which of the two distribution dominates: the maximum temperature reached by a crust with a strong organic component is lower than that reached by a purely silicatic crust.

  4. Spatial Complexity of Soil Organic Matter Forms at Nanometre Scales

    SciTech Connect

    Lehmann,J.; Solomon, D.; Kinyangi, J.; Dathe, L.; Wirick, S.; Jacobsen, C.

    2008-01-01

    Organic matter in soil has been suggested to be composed of a complex mixture of identifiable biopolymers1 rather than a chemically complex humic material2. Despite the importance of the spatial arrangement of organic matter forms in soil3, its characterization has been hampered by the lack of a method for analysis at fine scales. X-ray spectromicroscopy has enabled the identification of spatial variability of organic matter forms, but was limited to extracted soil particles4 and individual micropores within aggregates5, 6. Here, we use synchrotron-based near-edge X-ray spectromicroscopy7 of thin sections of entire and intact free microaggregates6 to demonstrate that on spatial scales below 50 nm resolution, highly variable yet identifiable organic matter forms, such as plant or microbial biopolymers, can be found in soils at distinct locations of the mineral assemblage. Organic carbon forms detected at this spatial scale had no similarity to organic carbon forms of total soil. In contrast, we find that organic carbon forms of total soil were remarkably similar between soils from several temperate and tropical forests with very distinct vegetation composition and soil mineralogy. Spatial information on soil organic matter forms at the scale provided here could help to identify processes of organic matter cycling in soil, such as carbon stability or sequestration and responses to a changing climate.

  5. Deformation behaviors of peat with influence of organic matter.

    PubMed

    Yang, Min; Liu, Kan

    2016-01-01

    Peat is a kind of special material rich in organic matter. Because of the high content of organic matter, it shows different deformation behaviors from conventional geotechnical materials. Peat grain has a non-negligible compressibility due to the presence of organic matter. Biogas can generate from peat and can be trapped in form of gas bubbles. Considering the natural properties of peat, a special three-phase composition of peat is described which indicates the existence of organic matter and gas bubbles in peat. A stress-strain-time model is proposed for the compression of organic matter, and the surface tension effect is considered in the compression model of gas bubbles. Finally, a mathematical model has been developed to simulate the deformation behavior of peat considering the compressibility of organic matter and entrapped gas bubbles. The deformation process is the coupling of volume variation of organic matter, gas bubbles and water drainage. The proposed model is used to simulate a series of peat laboratory oedometer tests, and the model can well capture the test results with reasonable model parameters. Effects of model parameters on deformation of peat are also analyzed. PMID:27247870

  6. Deformation behaviors of peat with influence of organic matter.

    PubMed

    Yang, Min; Liu, Kan

    2016-01-01

    Peat is a kind of special material rich in organic matter. Because of the high content of organic matter, it shows different deformation behaviors from conventional geotechnical materials. Peat grain has a non-negligible compressibility due to the presence of organic matter. Biogas can generate from peat and can be trapped in form of gas bubbles. Considering the natural properties of peat, a special three-phase composition of peat is described which indicates the existence of organic matter and gas bubbles in peat. A stress-strain-time model is proposed for the compression of organic matter, and the surface tension effect is considered in the compression model of gas bubbles. Finally, a mathematical model has been developed to simulate the deformation behavior of peat considering the compressibility of organic matter and entrapped gas bubbles. The deformation process is the coupling of volume variation of organic matter, gas bubbles and water drainage. The proposed model is used to simulate a series of peat laboratory oedometer tests, and the model can well capture the test results with reasonable model parameters. Effects of model parameters on deformation of peat are also analyzed.

  7. Diagenesis of Organic Matter in a Virginia Salt Marsh: Evaluation Through Compound Specific Isotope Analysis

    NASA Astrophysics Data System (ADS)

    Macko, S. A.; Geyer, M.

    2004-05-01

    Resolving the early diagenetic pathways to preservation of organic matter in a sedimentary sequence is one of the most intriguing challenges in organic geochemistry. What is preserved is usually ascribed to be either the product of retention of refractory materials or "protected" remnants of the destruction of the more labile matter, or more likely, a combination of both processes. A third mechanism, acquisition of newly synthesized material resulting from microbially mediated reactions, is less frequently invoked. In this study, the sources for the preserved organic matter and the sedimentary history of a Spartina marsh sequence on North Hog Island at the Virginia Coast Reserve Long Term Ecological Research (VCR-LTER) site are reported. Through the utilization of both carbon and nitrogen bulk isotopic compositions and compound specific isotopic analyses (CSIA) as well as the distributions of individual fatty acids, the depositional sequences are assessed. The variations in the cores for bulk organic carbon and nitrogen delta 13C and delta 15N typically ranged from -17 to -15 permil and +4 to +10 permil, respectively. The isotopic compositions generally show a trend of increasing in the heavy isotope downcore. These variations can be attributed to microbial utilization of amino acids resulting in bulk isotopic enrichments in deeper layers. Extensive microbial activity was evidenced at depth with increased amounts of odd-chain and branched-chain fatty acids. Overall, there is a decline with increasing depth in the amount of quantifiable fatty acids. Through the CSIA measurements, the original source of the preserved molecular components was observed to be essentially that of the Spartina, with loss of unsaturation deeper in the sequence. At greater depths, newly synthesized, longer-chain, unsaturated fatty acids were observed, possibly resulting from anaerobic pathways. Through mass balance using isotopic compositions of proposed bacterial endmember fatty acids, a

  8. Pyrogenic organic matter can alter microbial communication

    NASA Astrophysics Data System (ADS)

    Masiello, Caroline; Gao, Xiaodong; Cheng, Hsiao-Ying; Silberg, Jonathan

    2016-04-01

    Soil microbes communicate with each other to manage a large range of processes that occur more efficiently when microbes are able to act simultaneously. This coordination occurs through the continuous production of signaling compounds that are easily diffused into and out of cells. As the number of microbes in a localized environment increases, the internal cellular concentration of these signaling compounds increases, and when a threshold concentration is reached, gene expression shifts, leading to altered (and coordinated) microbial behaviors. Many of these coordinated behaviors have biogeochemically important outcomes. For example, methanogenesis, denitrification, biofilm formation, and the development of plant-rhizobial symbioses are all regulated by a simple class of cell-cell signaling molecules known as acyl homoserine lactones (AHLs). Pyrogenic organic matter in soils can act to disrupt microbial communication through multiple pathways. In the case of AHLs, charcoal's very high surface area can sorb these signaling compounds, preventing microbes from detecting each others' presence (Masiello et al., 2014). In addition, the lactone ring in AHLs is vulnerable to pH increases accompanying PyOM inputs, with soil pH values higher than 7-8 leading to ring opening and compound destabilization. Different microbes use different classes of signaling compounds, and not all microbial signaling compounds are pH-vulnerable. This implies that PyOM-driven pH increases may trigger differential outcomes for Gram negative bacteria vs fungi, for example. A charcoal-driven reduction in microbes' ability to detect cell-cell communication compounds may lead to a shift in the ability of microbes to participate in key steps of C and N cycling. For example, an increase in an archaeon-specific AHL has been shown to lead to a cascade of metabolic processes that eventually results in the upregulation of CH4 production (Zhang et al., 2012). Alterations in similar AHL compounds leads to

  9. Spectral band selection for classification of soil organic matter content

    NASA Technical Reports Server (NTRS)

    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.

  10. Interstellar chemistry recorded in organic matter from primitive meteorites.

    PubMed

    Busemann, Henner; Young, Andrea F; Alexander, Conel M O'd; Hoppe, Peter; Mukhopadhyay, Sujoy; Nittler, Larry R

    2006-05-01

    Organic matter in extraterrestrial materials has isotopic anomalies in hydrogen and nitrogen that suggest an origin in the presolar molecular cloud or perhaps in the protoplanetary disk. Interplanetary dust particles are generally regarded as the most primitive solar system matter available, in part because until recently they exhibited the most extreme isotope anomalies. However, we show that hydrogen and nitrogen isotopic compositions in carbonaceous chondrite organic matter reach and even exceed those found in interplanetary dust particles. Hence, both meteorites (originating from the asteroid belt) and interplanetary dust particles (possibly from comets) preserve primitive organics that were a component of the original building blocks of the solar system. PMID:16675696

  11. Assessment of soil organic matter fluxes at the EU level

    NASA Astrophysics Data System (ADS)

    Gobin, Anne; Campling, Paul

    2010-05-01

    Soil has a complex relationship with climate change. Soil helps take carbon dioxide out of the air and as such it absorbs millions of tons each year, but with the Earth still warming micro-organisms grow faster, consume more soil organic matter and release carbon dioxide. The net result is a relative decline in soil organic carbon. With a growing population and higher bio-energy demands, more land is likely to be required for settlement, for commercial activity and for bio-energy production. Conversions from terrestrial ecosystems to urban and commercial activity will alter both the production and losses of organic matter, and have an indirect impact on potential SOM levels. Conversions between different terrestrial ecosystems have a direct impact on SOM levels. Net SOM losses are reported for several land conversions, e.g. from grassland to arable land, from wetlands to drained agricultural land, from crop rotations to monoculture, reforestation of agricultural land. In the context of looking for measures to support best practices to manage soil organic matter in Europe we propose a method to assess soil organic matter fluxes at the EU level. We adopt a parsimonious approach that is comparable to the nutrient balance approaches developed by the OECD and Eurostat. We describe the methodology and present the initial results of a European carbon balance indicator that uses existing European statistical and land use change databases. The carbon balance consists of the following components: organic matter production (I), organic matter losses (O), land use changes that effect both production and losses (E). These components are set against the (mostly legislative) boundary conditions that determine the maximum input potential (MIP) for soil organic matter. In order to budget SOM losses due to mineralisation, runs will be made with a multi-compartment SOM model that takes into account management practices, climate and different sources of organic matter.

  12. Investigation of the organic matter in inactive nuclear tank liquids

    SciTech Connect

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

    1990-08-01

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

  13. Analysis of organic grain coatings in primitive interplanetary dust particles: Implications for the origin of Solar System organic matter

    NASA Astrophysics Data System (ADS)

    Flynn, George

    Analysis of organic grain coatings in primitive interplanetary dust particles: Implications for the origin of Solar System organic matter Chondritic, porous interplanetary dust particles (CP IDPs), the most primitive samples of extraterrestrial material available for laboratory analysis [1], are unequilibrated aggregates of mostly submicron, anhydrous grains of a diverse mineralogy. They contain organic matter not produced by parent body aqueous processing [2], some carrying H and N isotopic anomalies consistent with molecular cloud or outer Solar System material [3]. Scanning Transmission X-Ray Microscope (STXM) imaging at the C K-edge shows the individual grains in 10 micron aggregate CP IDPs are coated by a layer of carbonaceous material 100 nm thick. This structure implies a three-step formation sequence. First, individual grains condensed from the cooling nebular gas. Then complex, refractory organic molecules covered the surfaces of the grains either by deposition, formation in-situ, or a combination of both processes. Finally, the grains collided and stuck together forming the first dust-size material in the Solar System. Ultramicrotome sections, 70 to 100 nm thick were cut from several CP IDPs, embedded in elemental S to avoid exposure to C-based embedding media. X-ray Absorption Near Edge Structure (XANES) spectra were derived from image stacks obtained using a STXM. "Cluster analysis" was used to compare the C-XANES spectra from each of the pixels in an image stack and identify pixels exhibiting similar spectra. When applied to a CP IDP, cluster analysis identifies most carbonaceous grain coatings in a particle as having similar C-XANES spectra. Two processes are commonly suggested in the literature for production of organic grain coatings. The similarity in thickness and C-XANES spectra of the coatings on different minerals in the same IDP indicates the first, mineral specific catalysis, was not the process that produced these organic rims. Our results

  14. Characterizing Variability In Ohio River Natural Organic Matter

    EPA Science Inventory

    Surface water contains natural organic matter (NOM) which reacts with disinfectants creating disinfection byproducts (DBPs), some of which are USEPA regulated contaminants. Characterizing NOM can provide important insight on DBP formation and water treatment process adaptation t...

  15. Soil organic matter dynamics and the global carbon cycle

    SciTech Connect

    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[center dot]yr[sup -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.

  16. Soil organic matter dynamics and the global carbon cycle

    SciTech Connect

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

    1992-12-01

    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{center_dot}yr{sup -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.

  17. Seasonal Changes in Arctic Dissolved Organic Matter

    NASA Astrophysics Data System (ADS)

    Boot, C. M.; Wallenstein, M. D.; Schimel, J.

    2011-12-01

    The Arctic is a landscape in flux. Temperatures are shifting upward and plant communities are transitioning from tussock to shrub tundra in some regions. Decomposition processes sensitive to temperature, moisture, and plant inputs are controls on the source/sink dynamics of the Arctic C pool. The response of decomposition to warming will, in part, determine if the Arctic C pool feeds back positively or negatively to climate change. The portion of the C pool immediately available to decomposers is dissolved organic matter (DOM). The aim of this is study is to examine the molecular composition of DOM to determine which components vary seasonally in soil pore water among three vegetation types at Toolik Field Station in Alaska. Vegetation types include wet sedge (Carex aquatilis and Eriophorum angustifolium), moist acidic tussock (E. vaginatum) and shrub tundra (Betula nana and Salix sp.). These sites were sampled during winter/summer transitions in 2010 in order to capture both growing season and winter dynamics. We expected the chemical composition of DOM in pore water to be distinct among plant communities due to differences in root exudates, litter chemistry and microbial community; and vary seasonally due to shifting temperature and water availability and their impacts on decomposition of DOM. Soil pore water was isolated through centrifugation and is being characterized with ultra high performance liquid chromatography (UPLC) in line with a quadrupole time of flight mass spectrometer (QTOF-MS) as well as with specific UV absorbance at 254 nm (SUVA), and excitation emission matrices (EEMs) generated by fluorescence spectroscopy. The DOM concentrations across vegetation types show consistent seasonal patterns, spiking at thaw, and declining through late summer. As soils freeze these patterns diverge-in tussock soils DOM concentration decreases slightly, while in shrub and wet sedge sites it increases. SUVA values (indicator of aromaticity) were consistent among

  18. The fate of terrestrial organic matter in two Scottish sea lochs

    NASA Astrophysics Data System (ADS)

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

    2008-02-01

    Sea lochs are zones of rapid organic matter (OM) turnover. Most of this OM is of allochthonous origin, being introduced into the lochs via freshwater input. In this study the behaviour of terrestrially derived OM was elucidated using a combination of parameters which indicate OM diagenesis in the near surface sediments from two Scottish sea lochs, Loch Creran and Loch Etive. Alkaline CuO oxidation was used to determine lignin phenols which serve as biomarkers for terrestrial OM in sediments. Stable carbon isotope, total carbon and nitrogen and total OM (including the labile and refractory fractions) compositions were also determined. Lignin materials in the lochs were generally highly degraded and undergo little degradation further seaward. The vanillic acid to vanillin ratio, (Ad/Al)v in the lochs ranged from 0.52 to 2.69. However, there was a fraction of relatively fresh, land-derived OM, still undergoing degradation adding to the carbon cycling in the lochs, as indicated by the Rp values (ratio of refractory to total OM) and OC/N ratios in the surface sediments. The hydrological and hydrodynamic regimes in Loch Creran result in several phenomena such as the transportation of terrestrial debris via hydrodynamic sorting processes and the promotion of surface sediment diagenesis by bioturbation. Frequent water renewal results in better water circulation and oxygenation which facilitate OM decomposition. In Loch Etive the less frequent renewal gives rise to a more constant OM diagenesis along the loch.

  19. Composition and reactivity of ferrihydrite-organic matter associations

    NASA Astrophysics Data System (ADS)

    Eusterhues, Karin; Hädrich, Anke; Neidhardt, Julia; Küsel, Kirsten; Totsche, Kai

    2014-05-01

    The formation of organo-mineral associations affects many soil forming processes. On the one hand, it will influence soil organic matter composition and development, because the complex organic matter mixtures usually fractionate during their association with mineral surfaces. Whereas the associated fraction is supposed to be stabilized, the non-associated fraction remains mobile and available to degradation by microorganisms. On the other hand, the organic coating will completely change the interface properties of Fe oxides such as solubility, charge and hydrophobicity. This in turn will strongly influence their reactivity towards nutrients and pollutants, the adsorption of new organic matter, and the availability of ferric Fe towards microorganisms. To better understand such processes we produced ferrihydrite-organic matter associations by adsorption and coprecipitation in laboratory experiments. As a surrogate for dissolved soil organic matter we used the water-extractable fraction of a Podzol forest-floor layer under spruce. Sorptive fractionation of the organic matter was investigated by 13C NMR and FTIR. Relative to the original forest-floor extract, the ferrihydrite-associated OM was enriched in polysaccharides but depleted in aliphatic C and carbonyl C, especially when adsorption took place. Liquid phase incubation experiments were carried out with an inoculum extracted from the podzol forest-floor under oxic conditions at pH 4.8 to quantify the mineralization of the adsorbed and coprecipitated organic matter. These experiments showed that the association with ferrihydrite stabilized the associated organic matter, but that differences in the degradability of adsorbed and coprecipitated organic matter were small. We therefore conclude that coprecipitation does not lead to a significant formation of microbial inaccessible organic matter domains. Microbial reduction experiments were performed using Geobacter bremensis. We observed that increasing amounts of

  20. Organic matter dynamics and budgets in the turbidity maximum zone of the Seine Estuary (France)

    NASA Astrophysics Data System (ADS)

    Garnier, Josette; Billen, Gilles; Even, Stéphanie; Etcheber, Henri; Servais, Pierre

    2008-03-01

    Organic matter was studied in the turbidity maximum zone (TMZ) of the Seine Estuary during 8 tidal cycles from April to October in 2001, 2002 and 2003, covering a salinity range from 0 to 27. The hydrological conditions were quite varied (extremely wet in 2001, unusually dry in 2003). A particularly striking feature is the high organic matter content in the suspended solids (SS) of the Seine estuary (4-5%). By determining micro-organism activity and organic carbon partitioning, either linked to particles or in dissolved forms, and estimating the TMZ water volumes, together with SS, we extrapolated these activities and stocks to the whole TMZ. Carbon metabolism in the TMZ and fluxes upstream of the TMZ were compared on the dates of field surveys, and the routes and fate of carbon in the TMZ were quantified in order to learn about the trophic status of this estuarine zone in terms of autotrophy vs. heterotrophy. The upstream total organic carbon (TOC) fluxes (48% of particulate organic carbon (POC), 52% of dissolved organic carbon (DOC) on average) varied fourfold between the surveys, reaching the highest value of 280 TC d -1 during the wet summer of 2001; and the lowest value of about 70 TC d -1 in August 2003. Whereas nearly all of the DOC flux entering the TMZ reaches the coastal marine zone, mostly (at least 85%) in a refractory form, the POC accumulates in the TMZ of the estuarine channel, particle exportation being negligible. In the TMZ, biodegradation of DOC was, on average, much less (only a 2% decrease in the BDOC/DOC ratio between the TMZ upstream and downstream fluxes) than biodegradation of POC (11%). A simplified model of the TMZ (LIFT- Lumped Idealisation of the ecological Functioning in estuarine Turbidity maximum) was constructed for investigating the dynamics of organic matter on a seasonal scale. The agreement between observation and calculation allowed us to run sensitivity tests using new constraints; reductions of the upstream fluxes of

  1. Alteration of organic matter during infaunal polychaete gut passage and links to sediment organic geochemistry. Part I: Amino acids

    NASA Astrophysics Data System (ADS)

    Woulds, Clare; Middelburg, Jack J.; Cowie, Greg L.

    2012-01-01

    labelled glycine. Possible mechanisms for this enrichment include accumulation through inclusion in tissues with long residence times, preferential preservation (i.e. selection against) during metabolism, production from other labelled amino acids during varied metabolic processes, and accumulation in refractory by-products of secondary bacterial production. Overall, similarities were observed between amino-acid decay patterns in faunated microcosms, afaunal controls, and those previously reported in marine sediments. Thus, while polychaete gut passage did produce compound-selective accumulation and losses of certain amino acids in polychaete tissues and faecal matter, the impact of polychaete gut passage on sediment organic geochemistry was difficult to deconvolve from microbial decay. Despite processing large volumes of organic matter, polychaetes may not have distinctive influence on sediment compositions, possibly because metabolic processes concerning amino acids may be broadly similar across a wide range of organisms.

  2. The search for indigenous lunar organic matter.

    NASA Technical Reports Server (NTRS)

    Sagan, C.

    1972-01-01

    It is argued that the absence of organic compounds from returned lunar samples is to be expected even for a lunar history rich in primordial organics. The sites most likely to yield lunar organic compounds have not been investigated, and there may be an area of investigation conceivably critical to problems in prebiological chemistry and the early history of the solar system awaiting continued lunar exploration, manned or unmanned.

  3. High dimensional reflectance analysis of soil organic matter

    NASA Technical Reports Server (NTRS)

    Henderson, T. L.; Baumgardner, M. F.; Franzmeier, D. P.; Stott, D. E.; Coster, D. C.

    1992-01-01

    Recent breakthroughs in remote-sensing technology have led to the development of high spectral resolution imaging sensors for observation of earth surface features. This research was conducted to evaluate the effects of organic matter content and composition on narrowband soil reflectance across the visible and reflective infrared spectral ranges. Organic matter from four Indiana agricultural soils, ranging in organic C content from 0.99 to 1.72 percent, was extracted, fractionated, and purified. Six components of each soil were isolated and prepared for spectral analysis. Reflectance was measured in 210 narrow bands in the 400- to 2500-nm wavelength range. Statistical analysis of reflectance values indicated the potential of high dimensional reflectance data in specific visible, near-infrared, and middle-infrared bands to provide information about soil organic C content, but not organic matter composition. These bands also responded significantly to Fe- and Mn-oxide content.

  4. Impact of natural (storm) and anthropogenic (trawling) sediment resuspension on particulate organic matter in coastal environments

    NASA Astrophysics Data System (ADS)

    Pusceddu, A.; Grémare, A.; Escoubeyrou, K.; Amouroux, J. M.; Fiordelmondo, C.; Danovaro, R.

    2005-12-01

    In order to assess the impact of natural and anthropogenic sediment resuspension on quantity, biochemical composition and bioavailability of particulate organic matter (POM), two field investigations were carried out in two shallow coastal areas of the Mediterranean Sea. In the Gulf of Lions, we investigated the impact of a storm resuspension of sediment, whereas in the Thermaikos Gulf we investigated the impact of bottom trawling. Resuspension in the Gulf of Lions determined the increase of sedimentation rates, modified the composition of the organic fraction of settling particles and decreased the labile fraction of POM, as indicated by a drop in the enzymatically hydrolysable amino acid fraction. The increase in the refractory fraction, following short-term storm-induced resuspension, increased also the contribution of glycine and decreased the contribution of aspartic acid contents to the total amino acid pools. Trawling activities in Thermaikos Gulf determined a significant increase in suspended POM concentrations and important changes in its biochemical composition. After trawling, the protein to carbohydrate ratio decreased (as a result of a major input of sedimentary carbohydrates at the water-sediment interface) and the fraction of enzymatically hydrolysable biopolymeric C decreased by ≈30%, thus reducing the bioavailability of resuspended organic particles. Results of the present study indicate that changes in suspended POM, induced by storms and trawling activities, can have similar consequences on benthic systems and on food webs. In fact, the potential benefit of increased organic particle concentration for suspension feeders, is depressed by the shift of suspended food particles towards a more refractory composition.

  5. Modeling organic matter stabilization during windrow composting of livestock effluents.

    PubMed

    Oudart, D; Paul, E; Robin, P; Paillat, J M

    2012-01-01

    Composting is a complex bioprocess, requiring a lot of empirical experiments to optimize the process. A dynamical mathematical model for the biodegradation of the organic matter during the composting process has been developed. The initial organic matter expressed by chemical oxygen demand (COD) is decomposed into rapidly and slowly degraded compartments and an inert one. The biodegradable COD is hydrolysed and consumed by microorganisms and produces metabolic water and carbon dioxide. This model links a biochemical characterization of the organic matter by Van Soest fractionating with COD. The comparison of experimental and simulation results for carbon dioxide emission, dry matter and carbon content balance showed good correlation. The initial sizes of the biodegradable COD compartments are explained by the soluble, hemicellulose-like and lignin fraction. Their sizes influence the amplitude of the carbon dioxide emission peak. The initial biomass is a sensitive variable too, influencing the time at which the emission peak occurs. PMID:23393964

  6. Defining the quality of soil organic matter

    EPA Science Inventory

    Soils represent the largest terrestrial pool of carbon (C) and hold approximately two-thirds of all C held in these ecosystems. However, not all C in soils is of equal quality. Some fractions of the organic forms, i.e., soil organic carbon (SOC) have long residence times while ...

  7. Effects of Crayfish on Quality of Fine Particulate Organic Matter

    NASA Astrophysics Data System (ADS)

    Montemarano, J. J.; Kershner, M. W.; Leff, L. G.

    2005-05-01

    The origin and ontogeny of detritus often determines its bioavailability. Crayfish shred and consume detrital organic matter, influencing fine particulate organic matter (FPOM) availability, composition and quality. Given consumption of FPOM by many invertebrates, crayfish can indirectly affect these organisms by altering FPOM bioavailability through organic matter fragmentation, biofilm disturbance, and defecation. These effects may or may not vary among coarse particulate organic matter (CPOM) from different leaf species. To assess crayfish effects on FPOM quality, crayfish were fed stream-conditioned maple or oak leaves in hanging 1-mm mesh-bottom baskets in aquaria. After 12 h, crayfish and remaining leaves were removed. FPOM fragments that fell through the mesh were vacuum filtered and analyzed for percent organic matter, C:N ratio, and bacterial abundance. The same analyses were conducted on crayfish feces collected using finger cots encasing crayfish abdomens. C:N ratios did not differ between feces and maple leaf CPOM, but were lower in FPOM produced through fragmentation and disturbance (P = 0.023). Overall, crayfish alter the ontogeny of detritus, which may, in turn, affect stream FPOM dynamics.

  8. Soil organic matter contribution to the NW Mediterranean (Invited)

    NASA Astrophysics Data System (ADS)

    Kim, J.; Buscail, R.; Blokker, J.; Kerhervé, P.; Schouten, S.; Ludwig, W.; Sinninghe Damsté, J. S.

    2009-12-01

    The BIT (Branched and Isoprenoid Tetraether) index has recently been introduced as a proxy for soil organic matter input and is based on the relative abundance of non-isoprenoidal glycerol dialkyl glycerol tetraethers (GDGTs) derived from organisms living in terrestrial environments versus a structurally related isoprenoid GDGT “crenarchaeol” produced by marine Crenarchaeota (Hopmans et al., 2004). In this study, detailed spatial distribution patterns of BIT index were investigated in combination with other organic parameters in the continental margin of the north western Mediterranean. Based on a transect sampling strategy from source (land) to sink (sea) via river, we analysed a variety of soils from the Têt and Rhône basins, suspended particulate matter in waters of the Têt and Rhône rivers flowing into the Gulf of Lions, and marine surface sediments from the Gulf of Lions collected before and after a flood occurred in June 2008. Our study allows us to track BIT values along the transport pathway of soil organic matter and thus to estimate soil organic matter contribution in marine sediments in the Gulf of Lions (NW Mediterranean), a river-dominated continental margin. Hopmans, E.C., Weijers, J.W.H., Schefuss, E., Herfort, L., Sinninghe Damsté, J.S., Schouten, S., 2004. A novel proxy for terrestrial organic matter in sediments based on branched and isoprenoidtetraether lipids. Earth and Planetary Science Letters 224, 107-116.

  9. Dissolved Organic Matter in the Hudson River Plume

    NASA Astrophysics Data System (ADS)

    Chen, R. F.; Gardner, G. B.

    2004-12-01

    As part of the LATTE (Lagrangian Transport and Transformation Experiment) program, dissolved organic carbon (DOC), total nitrogen (TN), and chromophoric dissolved organic matter (CDOM) were measured in the Hudson River Estuary and Plume. As revealed by high resolution measurements from the Integrated Coastal Observation System (ICOS), dissolved organic matter has several sources within the estuary including the Hudson and Raritan Rivers, and a yet unidentified anthropogenic source off Manhattan. The quantity of dissolved organic matter that is exported from the Hudson River Estuary is significantly greater than that which the Hudson River can supply by simply conservative mixing with coastal seawater. In May, 2004, rhodamine dye was injected at the surface as the plume flowed out onto the New York/New Jersey shelf, once as the plume turned north towards Long Island, and once as the plume flowed south along the New Jersey coast. The ECOShuttle (a towed-undulating vehicle) carrying a rhodamine fluorometer was able to track these dye patches. An examination of dissolved organic matter transformations that occurred over these two to two and one-half day Lagrangian experiments will be discussed. In addition seasonal distributions of dissolved organic matter distributions will be presented from cruises in June 2003, June 2004 and September 2004 under different river flow and wind conditions.

  10. Recent updates on electrochemical degradation of bio-refractory organic pollutants using BDD anode: a mini review.

    PubMed

    Yu, Xinmin; Zhou, Minghua; Hu, Youshuang; Groenen Serrano, K; Yu, Fangke

    2014-01-01

    Boron-doped diamond (BDD) is playing an important role in environmental electrochemistry and has been successfully applied to the degradation of various bio-refractory organic pollutants. However, the review concerning recent progress in this research area is still very limited. This mini-review updated recent advances on the removal of three kinds of bio-refractory wastewaters including pharmaceuticals, pesticides, and dyes using BDD electrode. It summarized the important parameters in three electrochemical oxidation processes, i.e., anodic oxidation (AO), electro-Fenton (EF), and photoelectro-Fenton (PEF) and compared their different degradation mechanisms and behaviors. As an attractive improvement of PEF, solar photoelectro-Fenton using sunlight as UV/vis source presented cost-effectiveness, in which the energy consumption for enrofloxacin removal was 0.246 kWh/(g TOC), which was much lower than that of 0.743 and 0.467 kWh/(g TOC) by AO and EF under similar conditions. Finally the existing problems and future prospects in research were suggested. PMID:24777320

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

    NASA Technical Reports Server (NTRS)

    Mannino, Antonio; Harvey, H. Rodger

    2003-01-01

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

  12. Organic Matter Application Can Reduce Copper Toxicity in Tomato Plants

    ERIC Educational Resources Information Center

    Campbell, Brian

    2010-01-01

    Copper fungicides and bactericides are often used in tomato cultivation and can cause toxic Cu levels in soils. In order to combat this, organic matter can be applied to induce chelation reactions and form a soluble complex by which much of the Cu can leach out of the soil profile or be taken up safely by plants. Organic acids such as citric,…

  13. PHOTOCHEMICAL TRANSFORMATIONS OF DISSOLVED ORGANIC MATTER IN A BLACKWATER RIVER

    EPA Science Inventory

    We examined photochemical alterations of dissolved organic matter (DOM) from the Satilla River, a high DOC (10-40 mg/liter) blackwater river of southeast Georgia. Water samples were filtered to remove most organisms, placed in quartz tubes, and incubated under natural sunlight a...

  14. Pedogenesis evolution of mine technosols: focus onto organic matter implication

    NASA Astrophysics Data System (ADS)

    Grégoire, Pascaud; Marilyne, Soubrand; Laurent, Lemee; Husseini Amelène, El-Mufleh Al; Marion, Rabiet; Emmanuel, Joussein

    2014-05-01

    Keywords: Mine technosols, pedogenesis, organic matter, environmental impact, pyr-GC-MS Technosols include soils subject to strong anthropogenic pressure and particularly to soil influenced by human transformed materials. In this context, abandoned mine sites contain a large amount of transformed waste materials often enriched with metals and/or metalloids. The natural evolution of technosols (pedogenesis) may induces the change in contaminants behaviour in term of stability of bearing phases, modification of pH oxydo-reduction conditions, organic matter turnover, change in permeability, or influence of vegetation cover. The fate of these elements in the soil can induce major environmental problems (contamination of biosphere and water resource). This will contribute to a limited potential use of these soils, which represent yet a large area around the world. The initial contamination of the parental material suggests that the pedological cover would stabilize the soil; however, the chemical reactivity must be taken in consideration particularly with respect to potential metal leachings. In this case, it is quite important to understand the development of soil in this specific context. Consequently, the global aims of this study are to understand the functioning of mine Technosols focusing onto the organic matter implication in their pedogenesis. Indeed, soil organic matter constitutes an heterogeneous fraction of organic compounds that plays an important role in the fate and the transport of metals and metalloids in soils. Three different soil profiles were collected representative to various mining context (contamination, time, climat), respectively to Pb-Ag, Sn and Au exploitations. Several pedological parameters were determined like CEC, pH, %Corg, %Ntot, C/N ratio, grain size distribution and chemical composition. The evolution of the nature of organic matter in Technosol was studied by elemental analyses and thermochemolysis was realized on the total and

  15. Interstellar and Solar System Organic Matter Preserved in Interplanetary Dust

    NASA Astrophysics Data System (ADS)

    Messenger, Scott R.; Nakamura-Messenger, Keiko

    2015-08-01

    Interplanetary dust particles (IDPs) collected in the Earth’s stratosphere derive from collisions among asteroids and by the disruption and outgassing of short-period comets. Chondritic porous (CP) IDPs are among the most primitive Solar System materials. CP-IDPs have been linked to cometary parent bodies by their mineralogy, textures, C-content, and dynamical histories. CP-IDPs are fragile, fine-grained (< um) assemblages of anhydrous amorphous and crystalline silicates, oxides and sulfides bound together by abundant carbonaceous material. Ancient silicate, oxide, and SiC stardust grains exhibiting highly anomalous isotopic compositions are abundant in CP-IDPs, constituting 0.01 - 1 % of the mass of the particles. The organic matter in CP-IDPs is isotopically anomalous, with enrichments in D/H reaching 50x the terrestrial SMOW value and 15N/14N ratios up to 3x terrestrial standard compositions. These anomalies are indicative of low T (10-100 K) mass fractionation in cold molecular cloud or the outermost reaches of the protosolar disk. The organic matter shows distinct morphologies, including sub-um globules, bubbly textures, featureless, and with mineral inclusions. Infrared spectroscopy and mass spectrometry studies of organic matter in IDPs reveals diverse species including aliphatic and aromatic compounds. The organic matter with the highest isotopic anomalies appears to be richer in aliphatic compounds. These materials also bear similarities and differences with primitive, isotopically anomalous organic matter in carbonaceous chondrite meteorites. The diversity of the organic chemistry, morphology, and isotopic properties in IDPs and meteorites reflects variable preservation of interstellar/primordial components and Solar System processing. One unifying feature is the presence of sub-um isotopically anomalous organic globules among all primitive materials, including IDPs, meteorites, and comet Wild-2 samples returned by the Stardust mission. We will present

  16. GROUNDWATER TRANSPORT OF HYDROPHOBIC ORGANIC COMPOUNDS IN THE PRESENCE OF DISSOLVED ORGANIC MATTER

    EPA Science Inventory

    The effects of dissolved organic matter (DOM) on the transport of hydrophobic organic compounds in soil columns were investigated. Three compounds (naphthalene, phenanthrene and DDT) that spanned three orders of magnitude in water solubility were used. Instead of humic matter, mo...

  17. Compartmental model for organic matter digestion in facultative ponds.

    PubMed

    Giraldo, E; Garzón, A

    2002-01-01

    A model has been developed for the digestion of organic matter in facultative ponds in tropical regions. Complete mixing has been assumed for the aerobic and anaerobic compartments. Settling, aerobic layer oxidation, and anaerobic layer methanogenesis are the main processes for organic matter removal in the water column. Exchange processes between layers are dispersive or soluble exchange, solubilization and transport of organic matter from sediments to water column are also taken into account. Degradation of organic matter in the sediments produces gaseous emissions to the water column. The exchange between bubbles ascending and the water column was measured. The model was calibrated with data obtained from a pilot facultative pond built in Muña Reservoir in Bogotá. The pond was sampled during 4 months to compare data between its water hyacinth covered section and uncovered section. The results clearly show the relative importance of different BOD removal processes in facultative ponds and suggest modifications to further improve performance. The results from the model suggest that internal loadings to facultative ponds due to solubilization and return of organic matter from the sediments to the aerobic layer greatly influence the soluble BOD effluent concentration. Aerobic degradation activity in the facultative pond does not affect significantly the effluent concentration. Anaerobic degradation activity in the facultative pond can more easily achieve increases in the removal efficiencies of BOD.

  18. Compartmental model for organic matter digestion in facultative ponds.

    PubMed

    Giraldo, E; Garzón, A

    2002-01-01

    A model has been developed for the digestion of organic matter in facultative ponds in tropical regions. Complete mixing has been assumed for the aerobic and anaerobic compartments. Settling, aerobic layer oxidation, and anaerobic layer methanogenesis are the main processes for organic matter removal in the water column. Exchange processes between layers are dispersive or soluble exchange, solubilization and transport of organic matter from sediments to water column are also taken into account. Degradation of organic matter in the sediments produces gaseous emissions to the water column. The exchange between bubbles ascending and the water column was measured. The model was calibrated with data obtained from a pilot facultative pond built in Muña Reservoir in Bogotá. The pond was sampled during 4 months to compare data between its water hyacinth covered section and uncovered section. The results clearly show the relative importance of different BOD removal processes in facultative ponds and suggest modifications to further improve performance. The results from the model suggest that internal loadings to facultative ponds due to solubilization and return of organic matter from the sediments to the aerobic layer greatly influence the soluble BOD effluent concentration. Aerobic degradation activity in the facultative pond does not affect significantly the effluent concentration. Anaerobic degradation activity in the facultative pond can more easily achieve increases in the removal efficiencies of BOD. PMID:11833730

  19. Transplanting an organization: how does culture matter.

    PubMed

    Munich, Richard L

    2011-01-01

    Cultural differences are often cited as a major obstacle to the successful transition/integration into new situations of organizations. In this contribution, the author details the changing cultural factors impacting the operation and move of the Menninger Clinic from autonomous status to an affiliation with and first year of operation in the Baylor College of Medicine and Methodist Hospital Health Care System. Both functional and dysfunctional consequences are outlined, and specific examples illustrate how the organization's leadership and staff struggled to adapt during this complicated process. Based on the experience within the Clinic, general recommendations for managing such an acculturation are provided.

  20. Removal of dissolved organic matter by anion exchange: Effect of dissolved organic matter properties

    USGS Publications Warehouse

    Boyer, T.H.; Singer, P.C.; Aiken, G.R.

    2008-01-01

    Ten isolates of aquatic dissolved organic matter (DOM) were evaluated to determine the effect that chemical properties of the DOM, such as charge density, aromaticity, and molecular weight, have on DOM removal by anion exchange. The DOM isolates were characterized asterrestrial, microbial, or intermediate humic substances or transphilic acids. All anion exchange experiments were conducted using a magnetic ion exchange (MIEX) resin. The charge density of the DOM isolates, determined by direct potentiometric titration, was fundamental to quantifying the stoichiometry of the anion exchange mechanism. The results clearly show that all DOM isolates were removed by anion exchange; however, differences among the DOM isolates did influence their removal by MIEX resin. In particular, MIEX resin had the greatest affinity for DOM with high charge density and the least affinity for DOM with low charge density and low aromaticity. This work illustrates that the chemical characteristics of DOM and solution conditions must be considered when evaluating anion exchange treatment for the removal of DOM. ?? 2008 American Chemical Society.

  1. Organic matter on asteroid 130 Elektra

    NASA Technical Reports Server (NTRS)

    Cruikshank, D. P.; Brown, R. H.

    1987-01-01

    Infrared absorption spectra of a low-albedo water-rich asteroid appear to show a weak 3.4-micrometer carbon-hydrogen stretching mode band, which suggests the presence of hydrocarbons on asteroid 130 Elektra. The organic extract from the primitive carbonaceous chondritic Murchison meteorite shows similar spectral bands.

  2. A three-year time series of elemental and biochemical composition of organic matter in subtidal sandy sediments of the Ligurian Sea (northwestern Mediterranean)

    NASA Astrophysics Data System (ADS)

    Fabiano, M.; Danovaro, R.; Fraschetti, S.

    Variations in organic matter composition and microphytobenthic biomass were examined in the surface sandy sediments at a water depth of 10 m in the Gulf of Marconi (NW Mediterranean Sea) over a three year period. Seasonal changes in elemental (organic C and total N) and biochemical (lipids, proteins, carbohydrates) composition of sediment organic matter as well as Chla were assessed in order to provide information about the origin and fate of sedimentary organic matter, the contribution of microphytobenthic biomass, seasonal and interannual variations of food quantity and quality, and factors related to food availability. Data obtained in this three-year study revealed that organic matter determined with a muffle furnace is clearly an overestimate of the organic content of the sediment and is thus of little significance for benthic ecologists studying community dynamics in relation to food availability. Labile organic matter, utilized to estimate the food potentially available for benthic consumers, accounted for only a small percentage (on average less than 10%) of total organic C. The highest labile fraction was observed in spring, whereas minima were recorded in winter. Analysis of elemental and biochemical composition of organic matter showed an inverse relationship between amount of organic matter and its potential availability to consumers; small quantities of high-quality organic matter were replaced by large quantities of refractory material. The labile portion was mostly microphytobenthic (65% of the labile carbon). Protein: carbohydrate ratios were low and confirmed the role of proteins as a potentially limiting factor for consumers. Significant differences in nutritional quality of the sediment organic matter were observed from year to year, changes due to the increase in specific labile compound content.

  3. Organic matter in the Saturn system

    NASA Technical Reports Server (NTRS)

    Sagan, C.; Khare, B. N.; Lewis, J. S.

    1984-01-01

    Theoretical and experimental predictions of the formation (and outgassing) of organic molecules in the outer solar system are compared with Voyager IRIS spectral data for the Titan atmosphere. The organic molecules of Titan are of interest because the species and processes within the atmosphere of that moon may have had analogs in the early earth atmosphere 4 Gyr ago. The spacecraft data confirmed the presence of alkanes, ethane, propane, ethylene, alkynes, acetylene, butadiene, methylacetylene, nitriles, hydrogen cyanide, cyanoacetylene, and cyanogen, all heavier than the dominant CH4. Experimental simulation of the effects of UV photolysis, alpha and gamma ray irradiation, electrical discharges and proton and electron bombardment of similar gas mixtures has shown the best promise for modeling the reactions producing the Titan atmosphere chemicals.

  4. Organic matter preservation in the sediment of an acidic mining lake.

    PubMed

    Laskov, Christine; Amelung, Wulf; Peiffer, Stefan

    2002-10-15

    Sustainable management of acidic mining lakes requires knowledge on the origin and reactivity of its sedimentary organic matter. We identified different pools of organic matter (OM) in the Fe-rich sediment (up to 35 wt %) of an acidic (pH 2.8) mining lake using delta13C-signals, C/N ratios, and the markers alkanes, lignin-derived phenols, and benzenepolycarboxylic acids (BPCA). Additionally, a density fractionation was applied to each sediment layer. Three fractions, aquatic (AOM), terrestrial (TOM), and lignite-derived (LOM) organic matter, were discriminated, of which AOM comprises only a small fraction, with a minimum at the sediment bottom. The terrestrial contribution to sedimentary OM is higher than that of AOM but still low throughout the sediment core, whereas lignite-derived OM constitutes the major C-fraction, even in the upper sediment layers. The size of the carbon pools was quantified with a mass-balance approach, in which the BPCA content was utilized as an estimate for the lignite fraction in combination with the delta13C-signals of the three C fractions. The largest amount of OM was found in the heaviest (>2.4 g cm3) of the three density fractions of the two upper sediment layers, which implies strong interaction with iron hydroxides. Comparisons with C-oxidation rates revealed that besides the refractory origin of the OM, sorptive preservation by solid iron phases controls C-reactivity in the sediment and, hence, the internal neutralization capacity of the lake system.

  5. Dissolved Organic Matter in Headwater Streams: Compositional Variability across Climatic Regions of North America

    NASA Astrophysics Data System (ADS)

    Jaffé, R.; Yamashita, Y.; Maie, N.; Cooper, W. T.; Dittmar, T.; Dodds, W. K.; Jones, J. B.; Myoshi, T.; Ortiz-Zayas, J. R.; Podgorski, D. C.; Watanabe, A.

    2012-10-01

    Dissolved organic matter (DOM) represents the largest organic matter pool in freshwater systems, but much of it remains molecularly uncharacterized. Although freshwater systems cover only a small area of the earth's surface, inland waters are an important component of the global carbon cycle. The traditional idea that rivers are simply conduits for refractory carbon delivery to coastal areas is inconsistent with carbon flux estimates, and streams have been shown to serve as reactors for DOM cycling. The overall quality of DOM, and its associated reactivity, can be related to its chemical composition and molecular structure. However, the variability of DOM composition in freshwater ecosystems, particularly in headwater streams, is poorly characterized. Detailed molecular studies of DOM from small streams across climatic regions, which could provide critical information regarding carbon dynamics on a more global scale, have not been performed. To address these issues, this study applies a multi-method analytical approach in an attempt to assess molecular characteristics of DOM and ultrafiltered DOM (UDOM) in headwater streams from different climatic regions in North America. In general terms the chemical and molecular characteristics of UDOM from six different biomes were determined in unsurpassed detail to feature some clear general similarities but also specific differences. While the degree of similarity is remarkable, and suggests similar source strengths, such as soil-derived organic matter and/or similar diagenetic degradation processes for DOM from vastly different environments, each sample was clearly unique in its overall composition, featuring some distinct molecular patterns for at least one or more of the analytical determinations. Molecular and compositional differences of DOM from headwater streams should result from variations in DOM sources and localized environmental conditions, and consequently feature different photo- and bio-reactivity and

  6. Scavenging of soluble organic matter from the prebiotic oceans.

    PubMed

    Nissenbaum, A

    1976-12-01

    The existence of hot or cold "nutrient broth" or "primeval soup" is challenged on the basis of the recent geochemistry of soluble organic carbon in the oceans. Most of the dissolved organic carbon is recycled quickly by organisms, but the residual, biologically refractive, organic matter is efficiently scavenged from the oceans (residence time of 1000 to 3500 years) by nonbiologically mediated chemical and physical processes, such as adsorption on sinking minerals, polymerization and aggregation to humic type polymers or by aggregation to particulate matter through bubbling and sinking of this material to the ocean bottom. Since there is no reason to believe that such nonbiological scavenging was not operative in the prebiotic oceans as well, then the prolonged existence of "organic soup" is very doubtful. The question of the origin of life is thus assumed to be related to solid-liquid interfacial activity, and the answer may be associated with sediment-water interaction rather than with solution chemistry.

  7. Molecular insights into the microbial formation of marine dissolved organic matter: recalcitrant or labile?

    NASA Astrophysics Data System (ADS)

    Koch, B. P.; Kattner, G.; Witt, M.; Passow, U.

    2014-02-01

    The degradation of marine dissolved organic matter (DOM) is an important control variable in the global carbon cycle and dependent on the DOM composition. For our understanding of the kinetics of organic matter cycling in the ocean, it is therefore crucial to achieve a mechanistic and molecular understanding of its transformation processes. A long-term microbial experiment was performed to follow the production of non-labile DOM by marine bacteria. Two different glucose concentrations and dissolved algal exudates were used as substrates. We monitored the bacterial abundance, concentrations of dissolved and particulate organic carbon (DOC, POC), nutrients, amino acids, and transparent exopolymer particles (TEP) for two years. Ultrahigh resolution Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (FT-ICR-MS) allowed the molecular characterization of extracted DOM after 70 days and after ∼2 years of incubation. Although glucose was quickly degraded, a DOC background was generated in glucose incubations. Only 20% of the organic carbon from algal exudate was degraded within the 2 years of incubation. TEP, which are released by micro-organisms, were produced during glucose degradation but decreased within less than three weeks back to half of the maximum concentration and were below detection in all treatments after 2 years. The molecular analysis demonstrated that DOM generated during glucose degradation differed appreciably from DOM produced during the degradation of the algal exudates. Our results led to several conclusions: (i) Higher substrate levels result in a higher level of non-labile DOC which is an important prerequisite for carbon sequestration in the ocean; (ii) TEP are generated by bacteria but are also degraded rapidly, thus limiting their potential contribution to carbon sequestration; (iii) The molecular signatures of DOM derived from algal exudates or glucose after 70 days of incubation differed strongly from refractory DOM. After 2 years

  8. Influence of organic matter on collembolan communities in reedbed habitats

    NASA Astrophysics Data System (ADS)

    Uteseny, K.; Drapela, T.; Frouz, J.

    2009-04-01

    The combination of the organic matter, micro-climatic environments and plant cover belongs to important factors for the distribution of soil meso-fauna, especially Collembola. There are no studies attending to these factors on collembolan communities in reedbed vegetation. The main goals of our investigation were therefore to compare diversity of Collembola in redbed habitats of Lake Neudsiedl, eastern Austria, and to assess particularly the role of organic matter with regard to the collembolan community structure. Soil samples were taken from April 1997 to October 1997 at fifteen study sites covered with Phragmatis australis of different age. Changes in the structure and composition of the assemblages of Collembola were examined.

  9. Isotopic composition of hydrogen in insoluble organic matter from cherts

    NASA Technical Reports Server (NTRS)

    Krishnamurthy, R. V.; Epstein, S.

    1991-01-01

    Robert (1989) reported the presence of unusually enriched hydrogen in the insoluble HF-HCl residue extracted from two chert samples of Eocene and Pliocene ages. Since the presence of heavy hydrogen might be due to the incorporation of extraterrestrial materials, we desired to reexamine the same samples to isolate the D-rich components. Our experiments did not reveal any D-rich components, but the hydrogen isotope composition of the insoluble residue of the two chert samples was well within the range expected for terrestrial organic matter. We also describe a protocol that needs to be followed in the hydrogen isotope analysis of any insoluble organic matter.

  10. Andic soils : mineralogical effect onto organic matter dynamics, organic matter effect onto mineral dynamics, or both?

    NASA Astrophysics Data System (ADS)

    Basile-Doelsch, Isabelle; Amundson, Ronald; Balesdent, Jérome; Borschneck, Daniel; Bottero, Jean-Yves; Colin, Fabrice; de Junet, Alexis; Doelsch, Emmanuel; Legros, Samuel; Levard, Clément; Masion, Armand; Meunier, Jean-Dominique; Rose, Jérôme

    2014-05-01

    From a strictly mineralogical point of view, weathering of volcanic glass produces secondary phases that are short range ordered alumino-silicates (SRO-AlSi). These are imogolite tubes (2 to 3 nm of diameter) and allophane supposedly spheres (3.5 to 5 nm). Their local structure is composed of a curved gibbsite Al layer and Si tetrahedra in the vacancies (Q0). Proto-imogolites have the same local structure but are roof-shape nanoparticles likely representing the precursors of imogolite and allophanes (Levard et al. 2010). These structures and sizes give to the SRO-AlSi large specific surfaces and high reactivities. In some natural sites, imogolites and allophanes are formed in large quantities. Aging of these phases may lead to the formation of more stable minerals (halloysite, kaolinite and gibbsite) (Torn et al 1997). In natural environments, when the weathering of volcanic glass is associated with the establishment of vegetation, the soils formed are generally andosols. These soils are particularly rich in organic matter (OM), which is explained by the high ability of SRO-AlSi mineral phases to form bonds with organic compounds. In a first order "bulk" approach, it is considered that these bonds strongly stabilize the organic compounds as their mean age can reach more than 10 kyrs in some studied sites (Basile-Doelsch et al. 2005; Torn et al. 1997). However, the structure of the mineral phases present in andosols deserves more attention. Traditionally, the presence in the SRO-AlSi andosols was shown by selective dissolution approaches by oxalate and pyrophosphate. Using spectroscopic methods, mineralogical analysis of SRO-AlSi in andosols samples showed that these mineral phases were neither imogolites nor allophanes as originally supposed, but only less organized structures remained in a state of proto-imogolites (Basile-Doelsch al. 2005 ; Levard et al., 2012). The presence of OM would have an inhibitory effect on the formation of secondary mineral phases, by

  11. Negative priming effect on organic matter mineralisation in NE Atlantic slope sediments.

    PubMed

    Gontikaki, Evangelia; Thornton, Barry; Huvenne, Veerle A I; Witte, Ursula

    2013-01-01

    The priming effect (PE) is a complex phenomenon which describes a modification (acceleration or retardation) in the mineralisation rate of refractory organic matter (OM) following inputs of labile material. PEs are well-studied in terrestrial ecosystems owing to their potential importance in the evolution of soil carbon stocks but have been largely ignored in aquatic systems despite the fact that the prerequisite for their occurrence, i.e. the co-existence of labile and refractory OM, is also true for sediments. We conducted stable isotope tracer experiments in continental margin sediments from the NE Atlantic (550-950 m) to study PE occurrence and intensity in relation to labile OM input. Sediment slurries were treated with increasing quantities of the (13)C-labelled diatom Thalassiosira rotula and PE was quantified after 7, 14 and 21 days. There was a stepwise effect of diatom quantity on its mineralisation although mineralisation efficiency dropped with increasing substrate amounts. The addition of diatomaceous OM yielded a negative PE (i.e. retardation of existing sediment OM mineralisation) at the end of the experiment regardless of diatom quantity. Negative PE is often the result of preferential utilisation of the newly deposited labile material by the microbial community ("preferential substrate utilization", PSU) which is usually observed at excessive substrate additions. The fact that PSU and the associated negative PE occurred even at low substrate levels in this study could be attributed to limited amounts of OM subject to priming in our study area (~0.2% organic carbon [OC]) which seems to be an exception among continental slopes (typically >0.5%OC). We postulate that PEs will normally be positive in continental slope sediments and that their intensity will be a direct function of sediment OC content. More experiments with varying supply of substrate targeting C-poor vs. C-rich sediments are needed to confirm these hypotheses.

  12. Negative priming effect on organic matter mineralisation in NE Atlantic slope sediments.

    PubMed

    Gontikaki, Evangelia; Thornton, Barry; Huvenne, Veerle A I; Witte, Ursula

    2013-01-01

    The priming effect (PE) is a complex phenomenon which describes a modification (acceleration or retardation) in the mineralisation rate of refractory organic matter (OM) following inputs of labile material. PEs are well-studied in terrestrial ecosystems owing to their potential importance in the evolution of soil carbon stocks but have been largely ignored in aquatic systems despite the fact that the prerequisite for their occurrence, i.e. the co-existence of labile and refractory OM, is also true for sediments. We conducted stable isotope tracer experiments in continental margin sediments from the NE Atlantic (550-950 m) to study PE occurrence and intensity in relation to labile OM input. Sediment slurries were treated with increasing quantities of the (13)C-labelled diatom Thalassiosira rotula and PE was quantified after 7, 14 and 21 days. There was a stepwise effect of diatom quantity on its mineralisation although mineralisation efficiency dropped with increasing substrate amounts. The addition of diatomaceous OM yielded a negative PE (i.e. retardation of existing sediment OM mineralisation) at the end of the experiment regardless of diatom quantity. Negative PE is often the result of preferential utilisation of the newly deposited labile material by the microbial community ("preferential substrate utilization", PSU) which is usually observed at excessive substrate additions. The fact that PSU and the associated negative PE occurred even at low substrate levels in this study could be attributed to limited amounts of OM subject to priming in our study area (~0.2% organic carbon [OC]) which seems to be an exception among continental slopes (typically >0.5%OC). We postulate that PEs will normally be positive in continental slope sediments and that their intensity will be a direct function of sediment OC content. More experiments with varying supply of substrate targeting C-poor vs. C-rich sediments are needed to confirm these hypotheses. PMID:23840766

  13. Composition of dissolved organic matter in groundwater

    NASA Astrophysics Data System (ADS)

    Longnecker, Krista; Kujawinski, Elizabeth B.

    2011-05-01

    Groundwater constitutes a globally important source of freshwater for drinking water and other agricultural and industrial purposes, and is a prominent source of freshwater flowing into the coastal ocean. Therefore, understanding the chemical components of groundwater is relevant to both coastal and inland communities. We used electrospray ionization coupled with Fourier-transform ion cyclotron resonance mass spectrometry (ESI FT-ICR MS) to examine dissolved organic compounds in groundwater prior to and after passage through a sediment-filled column containing microorganisms. The data revealed that an unexpectedly high proportion of organic compounds contained nitrogen and sulfur, possibly due to transport of surface waters from septic systems and rain events. We matched 292 chemical features, based on measured mass:charge ( m/z) values, to compounds stored in the Kyoto Encyclopedia of Genes and Genomes (KEGG). A subset of these compounds (88) had only one structural isomer in KEGG, thus supporting tentative identification. Most identified elemental formulas were linked with metabolic pathways that produce polyketides or with secondary metabolites produced by plants. The presence of polyketides in groundwater is notable because of their anti-bacterial and anti-cancer properties. However, their relative abundance must be quantified with appropriate analyses to assess any implications for public health.

  14. Interstellar and Solar System Organic Matter Preserved in Interplanetary Dust

    NASA Technical Reports Server (NTRS)

    Messenger, Scott; Nakamura-Messenger, Keiko

    2015-01-01

    Interplanetary dust particles (IDPs) collected in the Earth's stratosphere derive from collisions among asteroids and by the disruption and outgassing of short-period comets. Chondritic porous (CP) IDPs are among the most primitive Solar System materials. CP-IDPs have been linked to cometary parent bodies by their mineralogy, textures, C-content, and dynamical histories. CP-IDPs are fragile, fine-grained (less than um) assemblages of anhydrous amorphous and crystalline silicates, oxides and sulfides bound together by abundant carbonaceous material. Ancient silicate, oxide, and SiC stardust grains exhibiting highly anomalous isotopic compositions are abundant in CP-IDPs, constituting 0.01 - 1 % of the mass of the particles. The organic matter in CP-IDPs is isotopically anomalous, with enrichments in D/H reaching 50x the terrestrial SMOW value and 15N/14N ratios up to 3x terrestrial standard compositions. These anomalies are indicative of low T (10-100 K) mass fractionation in cold molecular cloud or the outermost reaches of the protosolar disk. The organic matter shows distinct morphologies, including sub-um globules, bubbly textures, featureless, and with mineral inclusions. Infrared spectroscopy and mass spectrometry studies of organic matter in IDPs reveals diverse species including aliphatic and aromatic compounds. The organic matter with the highest isotopic anomalies appears to be richer in aliphatic compounds. These materials also bear similarities and differences with primitive, isotopically anomalous organic matter in carbonaceous chondrite meteorites. The diversity of the organic chemistry, morphology, and isotopic properties in IDPs and meteorites reflects variable preservation of interstellar/primordial components and Solar System processing. One unifying feature is the presence of sub-um isotopically anomalous organic globules among all primitive materials, including IDPs, meteorites, and comet Wild-2 samples returned by the Stardust mission.

  15. Caracterisation of anthropogenic contribution to the coastal fluorescent organic matter

    NASA Astrophysics Data System (ADS)

    El Nahhal, Ibrahim; Nouhi, Ayoub; Mounier, Stéphane

    2015-04-01

    It is known that most of the coastal fluorescent organic matter is of a terrestrial origin (Parlanti, 2000; Tedetti, Guigue, & Goutx, 2010). However, the contribution of the anthropogenic organic matter to this pool is not well defined and evaluated. In this work the monitoring of little bay (Toulon Bay, France) was done in the way to determine the organic fluorescent response during a winter period. The sampling campaign consisted of different days during the month of December, 2014 ( 12th, 15th, 17th, 19th) on 21 different sampling sites for the fluorescence measurements (without any filtering of the samples) and the whole month of December for the bacterial and the turbidity measurements. Excitation Emission Matrices (EEMs) of fluorescence (from 200 to 400 nm and 220 to 420 nm excitation and emission range) were treated by parallel factor analysis (PARAFAC).The parafac analysis of the EEM datasets was conducted using PROGMEEF software in Matlab langage. On the same time that the turbidity and bacterial measurement (particularly the E.Coli concentration) were determined. The results gives in a short time range, information on the the contribution of the anthropogenic inputs to the coastal fluorescent organic matter. In addition, the effect of salinity on the photochemical degradation of the anthropogenic organic matter (especially those from wastewater treatment plants) will be studied to investigate their fate in the water end member by the way of laboratory experiments. Parlanti, E. (2000). Dissolved organic matter fluorescence spectroscopy as a tool to estimate biological activity in a coastal zone submitted to anthropogenic inputs. Organic Geochemistry, 31(12), 1765-1781. doi:10.1016/S0146-6380(00)00124-8 Tedetti, M., Guigue, C., & Goutx, M. (2010). Utilization of a submersible UV fluorometer for monitoring anthropogenic inputs in the Mediterranean coastal waters. Marine Pollution Bulletin, 60(3), 350-62. doi:10.1016/j.marpolbul.2009.10.018

  16. Pre-biotic organic matter from comets and asteroids.

    PubMed

    Anders, E

    1989-11-16

    Several authors have suggested that comets or carbonaceous asteroids contributed large amounts of organic matter to the primitive Earth, and thus possibly played a vital role in the origin of life. But organic matter cannot survive the extremely high temperatures (>10(4) K) reached on impact, which atomize the projectile and break all chemical bonds. Only fragments small enough to be gently decelerated by the atmosphere--principally meteors of 10(-12)-10(-6) g--can deliver their organic matter intact. The amount of such 'soft-landed' organic carbon can be estimated from data for the infall rate of meteoritic matter. At present rates, only approximately 0.006 g cm-2 intact organic carbon would accumulate in 10(8) yr, but at the higher rates of approximately 4 x 10(9) yr ago, about 20 g cm-2 may have accumulated in the few hundred million years between the last cataclysmic impact and the beginning of life. It may have included some biologically important compounds that did not form by abiotic synthesis on Earth.

  17. Adsorption combined with ultrafiltration to remove organic matter from seawater.

    PubMed

    Tansakul, Chatkaew; Laborie, Stéphanie; Cabassud, Corinne

    2011-12-01

    Organic fouling and biofouling are the major severe types of fouling of reverse osmosis (RO) membranes in seawater (SW) desalination. Low pressure membrane filtration such as ultrafiltration (UF) has been developed as a pre-treatment before reverse osmosis. However, UF alone may not be an effective enough pre-treatment because of the existence of low-molecular weight dissolved organic matter in seawater. Therefore, the objective of the present work is to study a hybrid process, powdered activated carbon (PAC) adsorption/UF, with real seawater and to evaluate its performance in terms of organic matter removal and membrane fouling. The effect of different PAC types and concentrations is evaluated. Stream-activated wood-based PAC addition increased marine organic matter removal by up to 70% in some conditions. Moreover, coupling PAC adsorption with UF decreased UF membrane fouling and the fouling occurring during short-term UF was totally reversible. It can be concluded that the hybrid PAC adsorption/UF process performed in crossflow filtration mode is a relevant pre-treatment process before RO desalination, allowing organic matter removal of 75% and showing no flux decline for short-term experiments. PMID:21996607

  18. Adsorption combined with ultrafiltration to remove organic matter from seawater.

    PubMed

    Tansakul, Chatkaew; Laborie, Stéphanie; Cabassud, Corinne

    2011-12-01

    Organic fouling and biofouling are the major severe types of fouling of reverse osmosis (RO) membranes in seawater (SW) desalination. Low pressure membrane filtration such as ultrafiltration (UF) has been developed as a pre-treatment before reverse osmosis. However, UF alone may not be an effective enough pre-treatment because of the existence of low-molecular weight dissolved organic matter in seawater. Therefore, the objective of the present work is to study a hybrid process, powdered activated carbon (PAC) adsorption/UF, with real seawater and to evaluate its performance in terms of organic matter removal and membrane fouling. The effect of different PAC types and concentrations is evaluated. Stream-activated wood-based PAC addition increased marine organic matter removal by up to 70% in some conditions. Moreover, coupling PAC adsorption with UF decreased UF membrane fouling and the fouling occurring during short-term UF was totally reversible. It can be concluded that the hybrid PAC adsorption/UF process performed in crossflow filtration mode is a relevant pre-treatment process before RO desalination, allowing organic matter removal of 75% and showing no flux decline for short-term experiments.

  19. A marine sink for chlorine in natural organic matter

    NASA Astrophysics Data System (ADS)

    Leri, Alessandra C.; Mayer, Lawrence M.; Thornton, Kathleen R.; Northrup, Paul A.; Dunigan, Marisa R.; Ness, Katherine J.; Gellis, Austin B.

    2015-08-01

    Chloride--the most abundant ion in sea water--affects ocean salinity, and thereby seawater density and ocean circulation. Its lack of reactivity gives it an extremely long residence time. Other halogens are known to be incorporated into marine organic matter. However, evidence of similar transformations of seawater chloride is lacking, aside from emissions of volatile organochlorine by marine algae. Here we report high organochlorine concentrations from 180 to 700 mg kg-1 in natural particulate organic matter that settled into sediment traps at depths between 800 and 3,200 m in the Arabian Sea, taken between 1994 and 1995. X-ray spectromicroscopic imaging of chlorine bonding reveals that this organochlorine exists primarily in concentrated aliphatic forms consistent with lipid chlorination, along with a more diffuse aromatic fraction. High aliphatic organochlorine in particulate material from cultured phytoplankton suggests that primary production is a source of chlorinated organic matter. We also found that particulate algal detritus can act as an organic substrate for abiotic reactions involving Fe2+, H2O2 or light that incorporate chlorine into organic matter at levels up to several grams per kilogram. We conclude that transformations of marine chloride to non-volatile organochlorine through biological and abiotic pathways represent an oceanic sink for this relatively unreactive element.

  20. Search for Organic Matter in Leonid Meteoroids

    NASA Technical Reports Server (NTRS)

    Rairden, Richard L.; Jenniskens, Peter; Laux, Christophe O.; DeVincenzi, Donald L. (Technical Monitor)

    2000-01-01

    Near-ultraviolet 300-410 nm spectra of Leonid meteors were obtained in an effort to measure the strong B to X emission band of the radical CN in Leonid meteor spectra at 387 nm. CN is an expected product of ablation of nitrogen containing organic carbon in the meteoroids as well as a possible product of the aerothermochemistry induced by the kinetic energy of the meteor. A slitless spectrograph with objective grating was deployed on FISTA during the 1999 Leonid Multi-Instrument Aircraft Campaign. Fifteen first-order UV spectra were captured near the 02:00 UT meteor storm peak on November 18. It is found that neutral iron lines dominate the spectrum, with no clear sign of the CN band. The meteor plasma contains less than one CN molecule per three Fe atoms at the observed altitude of about 100 km.

  1. Aggregation of organic matter by pelagic tunicates

    SciTech Connect

    Pomeroy, L.R.; Deibel, D.

    1980-07-01

    Three genera of pelagic tunicates were fed concentrates of natural seston and an axenic diatom culture. Fresh and up to 4-day-old feces resemble flocculent organic aggregates containing populations of microorganisms, as described from highly productive parts of the ocean, and older feces resemble the nearly sterile flocculent aggregates which are ubiquitous in surface waters. Fresh feces consist of partially digested phytoplankton and other inclusions in an amorphous gelatinous matrix. After 18 to 36 h, a population of large bacteria develops in the matrix and in some of the remains of phytoplankton contained in the feces. From 48 to 96 h, protozoan populations arise which consume the bacteria and sometimes the remains of the phytoplankton in the feces. Thereafter only a sparse population of microorganisms remains, and the particles begin to fragment. Water samples taken in or below dense populations of salps and doliolids contained greater numbers of flocculent aggregates than did samples from adjacent stations.

  2. Analysis of the Organic Matter in Interplanetary Dust Particles: Clues to the Organic Matter in Comets, Asteroids, and Interstellar Grains

    NASA Technical Reports Server (NTRS)

    Flynn, G. J.; Keller, L. P.

    2003-01-01

    Reflection spectroscopy suggests the C- , P-, and D-types of asteroids contain abundant carbon, but these Vis-nearIR spectra are featureless, providing no information on the type(s) of carbonaceous matter. Infrared spectroscopy demonstrates that organic carbon is a significant component in comets and as grains or grain coatings in the interstellar medium. Most of the interplanetary dust particles (IDPs) recovered from the Earth s stratosphere are believed to be fragments from asteroids or comets, thus characterization of the carbon in IDPs provides the opportunity to determine the type(s) and abundance of organic matter in asteroids and comets. Some IDPs exhibit isotopic excesses of D and N-15, indicating the presence of interstellar material. The characterization of the carbon in these IDPs, and particularly any carbon spatially associated with the isotopic anomalies, provides the opportunity to characterize interstellar organic matter.

  3. Black Carbon in Estuarine (Coastal) High-molecular-weight Dissolved Organic Matter

    NASA Technical Reports Server (NTRS)

    Mannino, Antonio; Harvey, H. Rodger

    2003-01-01

    Dissolved organic matter (DOM) in the ocean constitutes one of the largest pools of organic carbon in the biosphere, yet much of its composition is uncharacterized. Observations of black carbon (BC) particles (by-products of fossil fuel combustion and biomass burning) in the atmosphere, ice, rivers, soils and marine sediments suggest that this material is ubiquitous, yet the contribution of BC to the ocean s DOM pool remains unknown. Analysis of high-molecular-weight DOM isolated from surface waters of two estuaries in the northwest Atlantic Ocean finds that BC is a significant component of DOM, suggesting that river-estuary systems are important exporters of BC to the ocean through DOM. We show that BC comprises 4-7% of the dissolved organic carbon (DOC) at coastal ocean sites, which supports the hypothesis that the DOC pool is the intermediate reservoir in which BC ages prior to sedimentary deposition. Flux calculations suggest that BC could be as important as vascular plant-derived lignin in terms of carbon inputs to the ocean. Production of BC sequesters fossil fuel- and biomass-derived carbon into a refractory carbon pool. Hence, BC may represent a significant sink for carbon to the ocean.

  4. Isotopic evidence for the contemporary origin of high-molecular weight organic matter in oceanic environments

    NASA Astrophysics Data System (ADS)

    Santschi, Peter H.; Guo, Laodong; Baskaran, M.; Trumbore, Susan; Southon, John; Bianchi, Thomas S.; Honeyman, Bruce; Cifuentes, Luis

    1995-02-01

    Previous work has suggested that apparent old 14C ages for oceanic DOC are the result of mixing of different organic carbon fractions. This report provides direct evidence for a contemporary 14C age of a high-molecular-weight (HMW) fraction of colloidal organic carbon (≥10 kD). Colloidal organic matter, COM 10 (from 10 kDaltons (kD) to 0.2 μm), isolated from the upper water column of the Gulf of Mexico and the Middle Atlantic Bight (MAB) region, generally has a contemporary age (i.e., younger than a few decades), while COM 1 (from 1 kD to 0.2 μm), is apparently old: 380-4500 y BP. Thus, BMW COM 10 (3-5% of DOC) from the upper water column is derived from living particulate organic matter (POM) and cycles rapidly, while a significant fraction of low-molecular-weight (≤1 kD) DOM is likely more refractory, and cycles on much longer time scales. The presence of pigment biomarker compounds in COM 1 from the upper water column points to selected phytoplankton species as one of the sources of COM. Terrestrial carbon as another source of COM is suggested from the inverse correlation between Δ 14C and δ 13C values, as well as the increasing δ 13C values with increasing salinity. 234Th-derived turnover times of COM 10 and COM 1 from both the Gulf of Mexico and MAB are consistently short, 1-20 and 3-30 days, respectively. These short residence times support the hypothesis that 14C ages of colloidal fractions of DOC are the result of COM fractions being a mixture of several endmembers with fast and slow turnover rates.

  5. The Relationship Between Dissolved Organic Matter Composition and Organic Matter Optical Properties in Freshwaters

    NASA Astrophysics Data System (ADS)

    Aiken, G.; Spencer, R. G.; Butler, K.

    2010-12-01

    Dissolved organic matter (DOM) chemistry and flux are potentially useful, albeit, underutilized, indicators of watershed characteristics, climate influences on watershed hydrology and soils, and changes associated with resource management. Source materials, watershed geochemistry, oxidative processes and hydrology exert strong influences on the nature and reactivity of DOM in aquatic systems. The molecules that comprise DOM, in turn, control a number of environmental processes important for ecosystem function including light penetration and photochemistry, microbial activity, mineral dissolution/precipitation, and the transport and reactivity of hydrophobic compounds and metals (e.g. Hg). In particular, aromatic molecules derived from higher plants exert strong controls on aquatic photochemistry, and on the transport and biogeochemistry of metals. Assessment of DOM composition and transport, therefore, can provide a basis for understanding watershed processes and biogeochemistry of rivers and streams. Here we present results of multi-year studies designed to assess the seasonal and spatial variability of DOM quantity and quality for 57 North American Rivers. DOM concentrations and composition, based on DOM fractionation on XAD resins, ultraviolet (UV)/visible absorption and fluorescence spectroscopic analyses, and specific compound analyses, varied greatly both between sites and seasonally within a given site. DOM in these rivers exhibited a wide range of concentration (<80 to >4000 µM C* L-1) and specific ultra-violet absorbance at 254 nm (SUVA254) (0.6 to 5 L *mg C-1 *m-1), an optical measurement that is an indicator of aromatic carbon content. In almost all systems, UV absorbance measured at specific wavelengths (e.g. 254 nm) correlated strongly with DOM and hydrophobic organic acid (HPOA) content (aquatic humic substances). The relationships between dissolved organic carbon (DOC) concentration and absorbance for the range of systems were quite variable due to

  6. Calculation of the enthalpy of formation of coal organic matter

    SciTech Connect

    A.M. Gyul'maliev; M.Ya. Shpirt

    2008-10-15

    The enthalpy of formation for the organic matter of coals in the coal rank series was calculated from the heat of the complete combustion reaction. Three variants were considered in which the experimental heating values and the values found from the correlation equation or calculated using the Mendeleev formula were taken as the heat of the complete combustion of coals.

  7. Photoproduction of Carbon Monoxide from Natural Organic Matter

    EPA Science Inventory

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

  8. Lyophilization and Reconstitution of Reverse Osmosis Concentrated Natural Organic Matter

    EPA Science Inventory

    Disinfection by-product (DBP) research can be complicated by difficulties in shipping large water quantities and changing natural organic matter (NOM) characteristics over time. To overcome these issues, it is advantageous to have a reliable method for concentrating and preservin...

  9. Quenching and Sensitizing Fullerene Photoreactions by Natural Organic Matter

    EPA Science Inventory

    Effects of natural organic matter (NOM) on the photoreaction kinetics of fullerenes (i.e., C60 and fullerenol) were investigated using simulated sunlight and monochromatic radiation (365 nm). NOM from several sources quenched (slowed) the photoreaction of C60 aggregates in water ...

  10. Organic matter in a coal ball: Peat or coal?

    USGS Publications Warehouse

    Hatcher, P.G.; Lyons, P.C.; Thompson, C.L.; Brown, F.W.; Maciel, G.E.

    1982-01-01

    Chemical analyses of morphologically preserved organic matter in a Carboniferous coal ball reveal that the material is coalified to a rank approximately equal to that of the surrounding coal. Hence, the plant tissues in the coal ball were chemically altered by coalification processes and were not preserved as peat. Copyright ?? 1982 AAAS.

  11. Isotopic composition of pyrite: Relationship to organic matter type and iron availability in some North American cretaceous shales

    USGS Publications Warehouse

    Gautier, D.L.

    1987-01-01

    The S isotope composition of pyrite in Cretaceous shales from the Western Interior of North America is related to organic C abundance, kerogen type and Fe availability. Both calcareous and noncalcareous rocks show a correlation between S and C, but noncalcareous rocks are relatively enriched in S with a higher S C ratio. This higher ratio probably shows that pyrite formation was Fe limited in the calcareous rocks. Organic-carbon-rich noncalcareous shales accumulated slowly beneath anoxic bottom waters. The anoxic bottom waters allowed hydrogen-rich organic matter to be preserved. Such shales have a narrow range of 34S-depleted sulfide and have Fe S ratios like stoichiometric pyrite, suggesting that pyrite formation in organic-rich shales was also limited by Fe availability. Conversely, organic-poor shales commonly accumulated at comparatively high rates, contain hydrogen-poor and refractory organic matter, and have a wide range of pyrite-S isotopic compositions. These organic-poor shales contain post-sulfidic authigenic minerals such as siderite and have excess reactive Fe rather than pyrite stoichiometry. Evidently Fe played a large role in early diagenesis and determined the course of post-sulfidic diagenesis. Fe availability was, however, mainly controlled by provenance, by the rates of sediment accumulation, and by the oxygen content of the depositional environment. ?? 1987.

  12. Fractionation of halogenated organic matter present in rain and snow

    PubMed

    Laniewski; Boren; Grimvall

    1999-01-01

    Organic matter in samples of rain and snow from Sweden, Poland, Germany and the Republic of Ireland was fractionated by employing a series of filtration, purging, evaporation and extraction steps. Determinations of the group parameter AOX (adsorbable organic halogens) in aqueous phases and EOX (extractable organic halogens) in organic phases showed that halogenated organic matter present in bulk precipitation is composed of several different groups of compounds. The largest amounts of organically bound halogens were found in fractions of relatively polar and non-volatile to semivolatile compounds. In particular, a significant part of the AOX could be attributed to alkaline-labile organic bases. Gas chromatographic analysis of different organic extracts in the chlorine channel of an atomic emission detector (AED) resulted in chromatograms with few distinct peaks, and analysis in the bromine channel did not produce any distinct peaks. Chlorinated acetic acids were the most abundant halogenated organic acids, and chlorinated alkyl phosphates were normally responsible for the largest peaks in the chlorine chromatogram of neutral, hexane-extractable compounds. When analysing volatiles, 1,4-dichlorobenzene and a thus far unidentified chloroorganic compound often caused the largest response in the chlorine channel of the AED system.

  13. CHROMOPHORIC DISSOLVED ORGANIC MATTER (CDOM) DERIVED FROM DECOMPOSITION OF VARIOUS VASCULAR PLANT AND ALGAL SOURCES

    EPA Science Inventory

    Chromophoric dissolved organic (CDOM) in aquatic environments is derived from the microbial decomposition of terrestrial and microbial organic matter. Here we present results of studies of the spectral properties and photoreactivity of the CDOM derived from several organic matter...

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

    EPA Science Inventory

    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...

  15. Molecular characterization of soil organic matter: a historic overview

    NASA Astrophysics Data System (ADS)

    Kögel-Knabner, Ingrid; Rumpel, Cornelia

    2014-05-01

    The characterization of individual molecular components of soil organic matter started in the early 19th century, but proceeded slowly. The major focus at this time was on the isolation and differentiation of different humic and fulvic acid fractions, which were considered to have a defined chemical composition and structure. The isolation and structural anlysis of specific individual soil organic matter components became more popular in the early 20th century. In 1936 40 different individual compounds had been isolated and a specific chemical strucutre had been attributed. These structural attributions were confirmed later for some, but not all of these individual compounds. In the 1950 much more individual compounds could be isolated and characterized, using complicated and time consuming chromatography. It became obvious that soil also contains a number of compounds of microbial origin, such as e.g., amino sugars and lipids. With the improvement of chrmoatographic separation techniques and the use of gas chromatography in combination with thin layerchromatography in the 1960 hundreds of individual compounds have been isolated and identified, most of them after chemical degradation of humic or fulvic acids. The chemical degradative techniques were amended with analytical pyrolysis in the 1970s. More and more, bulk soil organic matter was analyzed with these techniques and the advent of solid-stae 13C NMR spectroscopy around the 1980s allowed for the characterization of the composition of bulk soil organic matter. The gas chromatographic separation of organic matter can nowadays be combined with specific detectors, such that specific attributes ofindividual molecules can be analyzed, e.g. the radiocarbon content or the stable isotope composition.

  16. Comparison of polycyclic aromatic hydrocarbon distributions and sedimentary organic matter characteristics in contaminated, coastal sediments from Pensacola Bay, Florida.

    PubMed

    Simpson, Myrna J; Chefetz, Benny; Deshmukh, Ashish P; Hatcher, Patrick G

    2005-03-01

    In this study, we examined the distribution of polycyclic aromatic hydrocarbons (PAHs) in a contaminated coastal area and the characteristics of the natural organic matter in tandem. We present a detailed study of PAH concentration, distribution, and organic matter characteristics of three core samples from Pensacola Bay, Florida. Solid-state 13C Nuclear Magnetic Resonance (NMR), pyrolysis gas chromatography coupled with mass spectrometry (GC-MS), and tetramethyl ammonium hydroxide (TMAH) thermochemolysis GC-MS were applied to obtain structural details about the sedimentary organic matter. Elemental compositions (carbon and nitrogen) and estimates of black carbon contents are also reported. These coastal sediments were found to contain more PAHs in the upper 15 cm layers than in the bottom 15-25 cm samples. The samples that contained the most PAHs also contained the least amount of aromatic carbon and contained a significant amount of paraffinic carbon. Lignin-derived pyrolysis and TMAH thermochemolysis products were abundant and generally higher in all of the samples in comparison to those reported for modern coastal sediments, indicating a large flux of terrestrial carbon. The black carbon contents were found to range from 4.3% to 6.8%, which are significantly lower than other reports of black carbon in sediments, which represent as much as 65% of the total organic carbon content. The low black carbon content suggests that this type of refractory carbon may not be as responsible for regulating PAH distribution as indicated by other researchers.

  17. Identification and Characterization of Early Solar system Organic Matter Preserved in Chondritic Porous Interplanetary Dust Particles

    NASA Astrophysics Data System (ADS)

    Flynn, George; Wirick, Sue; Keller, Lindsay

    2015-04-01

    alternate model where carbon-bearing ices condense on the surfaces of grains, the ices are irradiated by ionizing radiation, and subsequent heating removes the ices leaving more refractory organic matter on the grain surfaces, as described by Bernstein et al. [4]. In one case we obtained C-, N-, and O-XANES spectra on the rim material. The O-XANES confirmed the presence of C=O. We found high N:C and O:C ratios that plot on the extension of the N:C vs. O:C correlation line, found in analysis of meteoritic organic matter [5], towards even more primitive organic matter than found in any meteorite. The organic rims are too thin for μ-FTIR spectroscopy, which is diffraction limited to about the wavelength/2, or ~2 μm for the aliphatic C-H stretching features. However, mid-infrared spectra obtained on CP IDPs show the presence of aliphatic C-H, C=O, C-C, and O-H, as well as crystalline and amorphous silicates [6]. Aromatic C-H is rarely detected in CP IDPs. Neither the organic rims nor the bulk organic matter in CP IDPs show the graphite exciton feature, whose strength in meteorite organic matter correlates with increasing parent body thermal metamorphism [7], indicating the organic matter in CP IDPs experienced minimal metamorphism after it formed. The spectra show variation in the aliphatic -C-H2- to -C-H3 and C=O to aliphatic C-H ratios from spot to spot on the same particle. C-XANES of ultramicrotome sections of CP IDPs also show significant variability, particularly in the C=O to C=C ratio. Variability in the C-XANES and the mid-infrared spectra indicates the organic matter in primitive CP IDPs consists of several compositionally distinct components. Our C-XANES and μ-FTIR results indicate the organic matter in CP IDPs is extremely primitive and that much of the pre-biotic organic matter of our Solar System formed early in the evolution of the Solar Nebula, by a process that preceded parent body aqueous processing. References: [1] Ishii, H. A. et al. (2008) Science, 319

  18. Organic matter variations in transgressive and regressive shales

    USGS Publications Warehouse

    Pasley, M.A.; Gregory, W.A.; Hart, G.F.

    1991-01-01

    Organic matter in the Upper Cretaceous Mancos Shale adjacent to the Tocito Sandstone in the San Juan Basin of New Mexico was characterized using organic petrology and organic geochemistry. Differences in the organic matter found in these regressive and transgressive offshore marine sediments have been documented and assessed within a sequence stratigraphic framework. The regressive Lower Mancos Shale below the Tocito Sandstone contains abundant well preserved phytoclasts and correspondingly low hydrogen indices. Total organic carbon values for the regressive shale are low. Sediments from the transgressive systems tract (Tocito Sandstone and overlying Upper Mancos Shale) contain less terrestrially derived organic matter, more amorphous non-structured protistoclasts, higher hydrogen indices and more total organic carbon. Advanced stages of degradation are characteristic of the phytoclasts found in the transgressive shale. Amorphous material in the transgressive shale fluoresces strongly while that found in the regressive shale is typically non-fluorescent. Data from pyrolysis-gas chromatography confirm these observations. These differences are apparently related to the contrasting depositional styles that were active on the shelf during regression and subsequent transgression. It is suggested that data from organic petrology and organic geochemistry provide greater resolution in sedimentologic and stratigraphic interpretations, particularly when working with basinward, fine-grained sediments. Petroleum source potential for the regressive Lower Mancos Shale below the Tocito Sandstone is poor. Based on abundant fluorescent amorphous material, high hydrogen indices, and high total organic carbon, the transgressive Upper Mancos Shale above the Tocito Sandstone possesses excellent source potential. This suggests that appreciable source potential can be found in offshore, fine-grained sediments of the transgressive systems tract below the condensed section and associated

  19. Characterisation of the organic matter pool in manures.

    PubMed

    Moral, R; Moreno-Caselles, J; Perez-Murcia, M D; Perez-Espinosa, A; Rufete, B; Paredes, C

    2005-01-01

    In this research, different types of animal manure were evaluated with respect to organic matter (OM), total organic carbon (C(ot)), total N (N(t)), C(ot)/N(t) ratio, water-soluble organic carbon (C(w)), organic N (N(org)), carbohydrates, C(w)/N(org) ratio, humic acid-like carbon (C(ha)), fulvic acid-like carbon (C(fa)), humification index ((C(ha)/C(ot))x100) (HI) and the C(ha)/C(fa) and NH(4)(+)-N/NO(3)(-)-N ratios. In comparison with the limits set by the Spanish legislation for organic fertilisers, most of the manures had high OM contents, moderate N(org) concentrations (except in the case of the chicken and pig manures where this parameter was high) and C(ot)/N(t) ratios above the value stated in the legislation. The study of the different fractions of organic matter showed that the horse, pig and rabbit manures had the greatest content of C(ot). However, the fraction of easily-biodegradable organic compounds (C(w)) was significantly higher in the horse, goat and chicken manures. The study also showed that, in most cases, the percentage of fulvic acid-like C was greater than that of the humic acid-like C, indicating that the organic matter of these wastes is not completely humified. Values of HI ((C(ha)/C(ot))x100) and C(ha)/C(fa) ratio in the studied manures were not significantly different. Regarding the parameters related to the organic matter stability such as C(w), carbohydrates and the C(ot)/N(t), C(w)/N(org) and NH(4)(+)-N/NO(3)(-)-N ratios, it has been determined that the organic matter of these materials was not completely stabilised. The heterogeneity in OM composition of the studied manures did not allow the formulation of simple equations for evaluation of the composition of these wastes from easily-determined parameters.

  20. Cumulative effects of biochar, mineral and organic fertilizers on soil organic matter

    NASA Astrophysics Data System (ADS)

    Plaza, César; López-de-Sá, Esther G.; Gascó, Gabriel; Méndez, Ana; Zaccone, Claudio

    2016-04-01

    We investigated the effect of three consecutive annual applications of biochar at rates of 0 and 20 t ha-1, in a factorial combination with a mineral fertilizer (NPK and nitrosulfate) and two types of organic amendment (municipal solid waste compost and sewage sludge), on soil organic matter in a field experiment under Mediterranean conditions. Biochar increased significantly soil organic C content and C/N ratio. In biochar-amended soils, soil organic C increased significantly with the addition of municipal solid waste compost and sewage sludge. To capture organic matter protection mechanisms related to aggregation and mineral interaction, the soil samples will be fractionated into free (unprotected), intra-macroaggregate, intra-microaggregate, and mineral-associated organic matter pools, and the isolated fractions will be subjected to further chemical and spectroscopic analysis.

  1. Pre-biotic organic matter from comets and asteroids

    NASA Technical Reports Server (NTRS)

    Anders, Edward

    1989-01-01

    Only meteoritic fragments small enough to be gently decelerated by the atmosphere (10 to the -12th g to 10 to the -6th g) can deliver organic matter intact. The amount of such 'soft-landed' organic carbon can be estimated from data for the infall rate of meteoritic matter. At present rates, only about 0.0006 g/sq cm intact organic carbon would accumulate in 100 million years, but at the higher rates of about four billion yr ago, about 20 g/sq cm may have accumulated in the few hundred million years between the last cataclysmic impact and the beginning of life. It may have included some biologically important compounds that did not form by abiotic synthesis on earth.

  2. Bacterial biomarkers thermally released from dissolved organic matter

    USGS Publications Warehouse

    Greenwood, P.F.; Leenheer, J.A.; McIntyre, C.; Berwick, L.; Franzmann, P.D.

    2006-01-01

    Hopane biomarker products were detected using microscale sealed vessel (MSSV) pyrolysis gas chromatography-mass spectrometry (GC-MS) analysis of dissolved organic matter from natural aquatic systems colonised by bacterial populations. MSSV pyrolysis can reduce the polyhydroxylated alkyl side chain of bacteriohopanepolyols, yielding saturated hopane products which are more amenable to GC-MS detection than their functionalised precursors. This example demonstrates how the thermal conditions of MSSV pyrolysis can reduce the biologically-inherited structural functionality of naturally occurring organic matter such that additional structural fragments can be detected using GC methods. This approach complements traditional analytical pyrolysis methods by providing additional speciation information useful for establishing the structures and source inputs of recent or extant organic material. ?? 2006.

  3. Nature of particulate organic matter in the River Indus, Pakistan

    NASA Astrophysics Data System (ADS)

    Ittekkot, Venugopalan; Arain, Rafee

    1986-08-01

    Suspended sediments from the Indus River collected during 1981 through 1983 were analyzed for POC and its constituent fractions including amino acids, amino sugars and sugars. Percentage of POC decreased with increasing suspended matter concentrations, which suggested dilution of organic matter by mineral matter. The concentrations of amino acids, amino sugars and sugars varied, respectively, between 180 and 2000 μg/l, 5 and 125 μg/l, and 60 and 1100 μg/l. Their contributions to POC varied between 2 and 60% for amino acids and amino sugars, and between 2 and 15% for sugars. They were high during low sediment discharge (February to June), and low during high sediment discharge (August and September). Suspended sediments associated with high sediment discharge periods were characterized by low ratios of: (i) aspartic acid:β-alanine (ii) glutamic acid:γ-aminobutyric acid (iii) amino acids:amino sugars (iv) hexoses:pentoses. These and the relative distribution pattern of the monosaccharides such as galactose, arabinose, mannose and xylose indicated that, not only dilution, but also differences in the sources and processes affect the POC transport in the Indus River. These result in transport of biodegraded organic matter during high sediment discharge periods: this appears to be common to other major rivers of the region, with depositional centers in deep sea areas. These rivers, with their high sediment loads, could contribute up to 8 to 11% of the global annual organic carbon burial in marine sediments.

  4. Mineral associations and nutritional quality of organic matter in shelf and upper slope sediments off Cape Hatteras, USA: a case of unusually high loadings

    NASA Astrophysics Data System (ADS)

    Mayer, L.; Benninger, L.; Bock, M.; DeMaster, D.; Roberts, Q.; Martens, C.

    Relationships among organic carbon (OC), enzymatically hydrolyzable amino acid (EHAA) concentrations and mineral surface area (SFA) were assessed for sediments from the shelf and slope region near Cape Hatteras, USA. Grain size, measured here as mineral-specific surface area, explained 55% of the variance in organic matter concentrations. Organic loadings, as ratios of organic carbon to surface area (OC:SFA), decrease with water column and core depth. OC:SFA ratios in this region are comparable to those found in areas with anoxic water columns, and are the highest reported for shelf-slope sediments underlying oxygenated water columns. With increasing water-column depth, organic matter becomes progressively incorporated into low-density (<2.4 g cm -3), organomineral aggregates, reflecting the increase in clay content in sediments with water-column depth. Organic coverage of mineral surfaces was determined by gas sorption methods; throughout the depth range minerals are essentially bare of organic coatings, in spite of high organic loadings. EHAA concentrations increase with water-column depth in a similar fashion as OC concentrations, and help to support intense heterotrophic communities at depth. Rapidly decreasing ratios of EHAA to total organic matter with water-column depth are consistent with previous inferences that largely refractory organic matter is exported from the shelf to the slope. Significant burial of EHAA downcore indicates protection of enzymatically hydrolyzable biopolymers with depth.

  5. Photoelectrocatalytic decontamination of oilfield produced wastewater containing refractory organic pollutants in the presence of high concentration of chloride ions.

    PubMed

    Li, Guiying; An, Taicheng; Chen, Jiaxin; Sheng, Guoying; Fu, Jiamo; Chen, Fanzhong; Zhang, Shanqing; Zhao, Huijun

    2006-11-16

    The feasibility study of the application of the photoelectrocatalytic decontamination of high saline produced water containing refractory organic pollutants was investigated in the slurry photoelectrocatalytic reactor with nanometer TiO2 particle prepared with sol-gel method using the acetic acid as hydrolytic catalyst. The efficiency of the photoelectrocatalytic decontamination of produced water was determined with both COD removal from the tested wastewater and the decrease of mutagenic activity evaluated by Ames tests. The experimental results showed that the photoelectrocatalysis is a quite efficient process for decontaminating the produced water, although there are high concentration of salt existed in oilfield wastewater. We found that the COD removal efficiencies by photoelectrocatalytic process are much higher than that of by photocatalytic or electrochemical oxidation individually in the photoelectrocatalytic reactor. The COD removal can be substantially improved by the added H2O2 and the generation of active chlorine from high concentration chlorides in the wastewater. The effects of various operating conditions, such as initial COD concentration, applied cell voltage, catalyst amount and initial pH value of solution, on the photoelectrocatalytic efficiencies, is also investigated in detail. The results showed that when the raw produced wastewater was diluted in a 1:1 (v/v) ratio, there is a highest COD removal efficiency. And the photoelectrocatalytic degradation of organic pollutants in saline water is much favored in acidic solution than that in neutral and/or alkaline solution. PMID:16875777

  6. Submicron Organic Matter in a Peri-alpine, Ultra-oligotrphic Lake

    SciTech Connect

    Chanudet,V.; Filella, M.

    2007-01-01

    Combining organic carbon (OC) measurements with the classic MBTH (3-methyl-2-benzothiazolinone hydrochloride) method for carbohydrate determination and a new voltammetric method for the determination of refractory organic matter (ROM) made it possible, for the first time, to quantify the types, sources and fate of submicron organic matter present in an ultra-oligotrophic lake (Lake Brienz, Switzerland). The lake is extremely rich in suspended glacial flour in summer (glacier melting season). Measurements were taken from June 2004 to October 2005 from 1.2 {mu}m filtered samples. OC concentration remained extremely low throughout the year (below 1 mg C L{sup -1}). MBTH carbohydrate concentration was very low in the lake (0.06-0.43 mg C L{sup -1}) and in the two tributary rivers (0.06-0.25 mg C L{sup -1}). Lake carbohydrate concentration only correlated with phytoplanktonic biomass at the onset of the productivity period. The results suggest that differences in MBTH concentration may sometimes reflect differences in the nature of the carbohydrates rather than differences in carbon concentration. Extensive fibril formation was evidenced by transmission electron microscopy (TEM) observations. ROM concentration in the lake was also very low (0.1-0.2 mg C L{sup -1}). Significant variation in ROM riverine input was due to either annual occurrences (snow melting) or irregular episodes (floods). Melting snow was responsible for about 30% of the lake's annual ROM input. One box mass balance calculations showed that about 25% of ROM was lost within the lake. Evidence gleaned from TEM and STXM (scanning transmission X-ray microscopy) observations clearly indicates that this is mainly caused by ROM sedimentation after association with inorganic colloids.

  7. Influences of sedimentary organic matter quality on the bioaccumulation of 4-nonylphenol by estuarine amphipods.

    PubMed

    Hecht, Scott A; Gunnarsson, Jonas S; Boese, Bruce L; Lamberson, Janet O; Schaffner, Christian; Giger, Walter; Jepson, Paul C

    2004-04-01

    Nonylphenol (NP) is a moderately persistent, hydrophobic chemical with endocrine-disrupting and acute narcotic effects in aquatic biota. Concern exists about the ultimate fate of NP in aquatic ecosystems and the potential for bioaccumulation by benthic biota from the sediment with the potential for further transfer to higher trophic levels. Our goals were to determine if benthic amphipods bioaccumulate significant amounts of NP from sediment and to determine how additions of organic matter influence NP bioaccumulation by amphipods. Estuarine sediment was spiked with 14C-NP and enriched with two types of organic carbon (OC) sources of different nutritional qualities. Macrophytic algae (Ulva species) were used as a labile and nutritious OC source. Wood lignins were used as a refractory and low-nutrition OC source. Nonylphenol bioaccumulation was measured in Eohaustorius estuarius, Grandidierella japonica, and Corophium salmonis after 16 d of exposure. Nonylphenol accumulation was inversely proportional to OC quantity, but was unaffected by OC nutritional quality. Significant differences were found in the accumulation patterns between the three amphipod species. Mean biota-sediment accumulation factors ranged from 8.1 to 33.9 in E. estuarius, from 4.6 to 17.2 in G. japonica, and averaged 7.1 in male C. salmonis and 16.0 in female C. salmonis. These accumulation factors indicate that estuarine amphipods could constitute an important source of NP to higher trophic levels, such as juvenile fish. PMID:15095881

  8. Loss of organic matter from riverine particles in deltas

    SciTech Connect

    Keil, R.G.; Quay, P.D.; Richey, J.E.

    1997-04-01

    In order to examine the transport and burial of terrigenous organic matter along the coastal zones of large river systems, we assessed organic matter dynamics in coupled river/delta systems using mineral surface area as a conservative tracer for discharged riverine particulate organic matter (POM). Most POM in the rivers studied (n = 6) is tightly associated with suspended mineral materiaL e.g., it is sorbed to mineral surfaces. Average organic loadings in the Amazon River (0.67 - 0.14 Mg C m{sup -2}), the river for which we have the largest dataset, are approximately twice that of sedimentary minerals from the Amazon Delta (-0.35 mg C m{sup -2}). Stable carbon isotope analysis indicate that approximately two-thirds of the total carbon on the deltaic particles is terrestrial. The combined surface-normalized, isotope-distinguished estimate is that >70% of the Amazon fluvial POM is not buried in the delta consistent with other independent evidence. Losses of terrestrial POM have also been quantified for the river/delta systems of Columbia in the USA, Fly in New Guinea. and Huange-He in China. If the losses of riverine POM observed in these river/delta systems are representative of rivers worldwide, then the surface-constrained analyses point toward a global loss of fluvial POM in delta regions of {approximately}0.1 x 10{sup 15} g C y{sup -1}. 28 refs., 2 figs., 1 tab.

  9. Natural organic matter as global antennae for primary production.

    PubMed

    Van Trump, J Ian; Rivera Vega, Fransheska J; Coates, John D

    2013-05-01

    Humic substances (HS) are high-molecular-weight complex refractory organics that are ubiquitous in terrestrial and aquatic environments. While resistant to microbial degradation, these compounds nevertheless support microbial metabolism via oxidation or reduction of their (hydro)quinone moieties. As such, they are known to be important electron sinks for respiratory and fermentative bacteria and electron sources for denitrifying and perchlorate-reducing bacteria. HS also strongly promote abiotic reduction of Fe(III) when irradiated with light. Here, we show that HS-enhanced Fe(III) photoreduction can also drive chemolithotrophic microbial respiration by producing Fe(II), which functions as a respiratory electron donor. Due to their molecular complexity, HS absorb most of the electromagnetic spectrum and can act as broad-spectrum antennae converting radiant energy into bioavailable chemical energy. The finding that chemolithotrophic organisms can utilize this energy has important implications for terrestrial, and possibly extraterrestrial, microbial processes and offers an alternative mechanism of radiation-driven primary productivity to that of phototrophy.

  10. Microbial decomposition of terrigenic organic matter discharged into the Baltic Sea

    NASA Astrophysics Data System (ADS)

    Manecki, M.; Herlemann, D.; Pollehne, F.; Labrenz, M.; Zimmermann, R.; Dittmar, T.; Schulz-Bull, D.; Jürgens, K.

    2012-04-01

    The permafrost soils in arctic regions contain a large amount of the worldwide organic carbon and global warming is expected to increase drainage of dissolved organic matter (DOM) into the adjacent oceans. It is yet unclear how this terrigenic organic matter will influence the global carbon cycle and the feedback effects to the climate. We used the Baltic Sea as a model system to investigate the role of abiotic factors on the degradation of terrigenic dissolved organic matter (tDOM) upon discharge into a brackish system as well as the response of the microbial community. Water from the Kalix River in Northern Sweden, which drains also permafrost soils, was used as the tDOM source in incubation experiments with Baltic Sea water. Different qualities of tDOM were compared by applying concentration procedures: tDOM was added to fresh Baltic Sea water as untreated Kalix River water or concentrated by commonly use DOC concentration procedures (lyophilization, ultrafiltration, solid phase extraction). We investigated the TDOC degradation by parallel measurements of dissolved organic carbon (DOC) consumption, DOM composition (using a 15 Tesla Fourier Transformation Ion Cyclotron Resonance Mass Spectrometer (FT-ICR-MS)), microbial activities and microbial community structure. FT-ICR-MS measurements showed qualitative differences in the DOM compositions for the different treatments and a drastic change in DOM composition between the third and fourth week of the incubation experiment. Despite the qualitative differences in DOM composition, the results obtained so far revealed that the added tDOC had, independent of the previous enrichment procedure, only little influence on bacterial activities, bacterial community structure and DOC decomposition dynamics. This indicates that the major portion of the added tDOC is of refractory nature. Instead, bacterial predation by heterotrophic protists had a strong impact on both bacterial community structure and DOC decomposition

  11. Relating hygroscopicity and composition of organic aerosol particulate matter

    SciTech Connect

    Duplissy, J.; DeCarlo, P. F.; Dommen, J.; Alfarra, M. R.; Metzger, A.; Barmpadimos, I.; Prevot, A. S. H.; Weingartner, E.; Tritscher, T.; Gysel, M.; Aiken, A. C.; Jimenez, J. L.; Canagaratna, M. R.; Worsnop, D. R.; Collins, D. R.; Tomlinson, J.; Baltensperger, U.

    2011-01-01

    A hygroscopicity tandem differential mobility analyzer (HTDMA) was used to measure the water uptake (hygroscopicity) of secondary organic aerosol (SOA) formed during the chemical and photochemical oxidation of several organic precursors in a smog chamber. Electron ionization mass spectra of the non-refractory submicron aerosol were simultaneously determined with an aerosol mass spectrometer (AMS), and correlations between the two different signals were investigated. SOA hygroscopicity was found to strongly correlate with the relative abundance of the ion signal m/z 44 expressed as a fraction of total organic signal (f44). m/z 44 is due mostly to the ion fragment CO2+ for all types of SOA systems studied, and has been previously shown to strongly correlate with organic O/C for ambient and chamber OA. The analysis was also performed on ambient OA from two field experiments at the remote site Jungfraujoch, and the megacity Mexico City, where similar results were found. A simple empirical linear relation between the hygroscopicity of OA at subsaturated RH, as given by the hygroscopic growth factor (GF) or "κorg" parameter, and f44 was determined and is given by κorg = 2.2 × f44 - 0.13. This approximation can be further verified and refined as the database for AMS and HTDMA measurements is constantly being expanded around the world. Finally, the use of this approximation could introduce an important simplification in the parameterization of hygroscopicity of OA in atmospheric models, since f44 is correlated with the photochemical age of an air mass.

  12. Role of organic matter in framboidal pyrite oxidation.

    PubMed

    Rigby, P A; Dobos, S K; Cook, F J; Goonetilleke, A

    2006-08-31

    An experimental system has been set up to investigate the reaction kinetics of framboidal pyrite oxidation in real, reactive acid sulfate soil assemblages. This study was undertaken to determine the degree to which pyrite oxidation rates are reduced by bacteriological reactions and organic matter, which both modify the net reaction mechanisms and compete for available oxygen. The results from these experimental runs not only confirm the role of organic matter in mitigating pyrite oxidation but indicate that at least initially, the acidity produced is consumed or otherwise ameliorated by parallel reactions. Tracking pH or [H+] in both a reactor and in soil does not accurately reflect reaction progress and may not correctly indicate the true level of risk. In comparison, the tracking of pyrite oxidation with the concentration of sulfate in solution is not affected by side reactions or precipitation and is therefore a better indicator for the rate of pyrite destruction. PMID:16839593

  13. Carbon isotopic studies of organic matter in precambrian rocks.

    PubMed

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

    1972-03-17

    Reduced carbon in early Precambrian cherts of the Fig Tree and upper and middle Onverwacht groups of South Africa is isotopically similar (the average value of delta(13)C(PDB) is -28.7 per mil) to photosynthetically produced organic matter of younger geological age. Reduced carbon in lower Onverwacht cherts (Theespruit formation) is anomalously heavy (the average value of delta(13)C(PDB) is -16.5 per mil). This discontinuity may reflect a major event in biological evolution.

  14. Degradation of refractory dibutyl phthalate by peroxymonosulfate activated with novel catalysts cobalt metal-organic frameworks: Mechanism, performance, and stability.

    PubMed

    Li, Huanxuan; Wan, Jinquan; Ma, Yongwen; Wang, Yan; Chen, Xi; Guan, Zeyu

    2016-11-15

    In this work, a new effective and relatively stable heterogeneous catalyst of Metal-Organic Framework Co3(BTC)2·12H2O (Co-BTC) has been synthesized and tested to activate peroxymonosulfate (PMS) for removal of refractory dibutyl phthalate (DBP). Co-BTC(A) and Co-BTC(B) were synthesized by different methods, which resulted in different activity towards PMS. The results indicated that Co-BTC(A) showed better performance on DBP degradation. The highest degradation rate of 100% was obtained within 30min. The initial pH showed respective level on DBP degradation with a rank of 5.0>2.75>9.0>7.0>11.0 in PMS/Co-BTC(A) system. No remarkable reduction of DBP was observed in the catalytic activity of Co-BTC(A) at 2nd run as demonstrated by recycling. However, the DBP degradation efficiency decreased by 8.26%, 10.9% and 25.6% in the 3rd, 4th, and 5th runs, respectively. The loss of active catalytic sites of Co(II) from Co-BTC(A) is responsible for the activity decay. Sulfate radicals (SO4(-)) and hydroxyl radicals (OH) were found at pH 2.75. Here, we propose the possible mechanism for activation of PMS by Co-BTC(A), which is involved in homogeneous and heterogeneous reactions in the solutions and the surface of Co-BTC(A), respectively. PMID:27420387

  15. Photochemical Degradation of Persistent Organic Pollutants: A Study of Ice Photochemistry Mediated by Dissolved Organic Matter

    NASA Astrophysics Data System (ADS)

    Bobby, R.; Pagano, L.; Grannas, A. M.

    2012-12-01

    It is well established that ice is a reactive medium in the environment and that active photochemistry occurs in frozen systems. Snow and ice contain a number of absorbing species including nitrate, peroxide and organic matter. Upon irradiation, they can generate a variety of reactive intermediates such as hydroxyl radical and singlet oxygen. It has been shown that dissolved organic matter is a ubiquitous component of snow and ice and plays an important role in overall light absorption properties of the sample. Additionally, the reactive intermediates produced can further react with contaminants present and alter their fate in the environment. Unfortunately, the role of dissolved organic matter in ice photochemistry has received little attention. Here we present results from laboratory-based studies aimed at elucidating the role of dissolved organic matter photochemistry on contaminant degradation in ice. Aqueous samples of our target pollutant, aldrin (20 μg/L), in liquid and frozen phases, were irradiated under Q-Panel 340 lamps to simulate the UV radiation profile of natural sunlight. Results indicated that frozen samples degraded more quickly than liquid samples and that the addition of dissolved organic matter increases the aldrin degradation rate significantly. Both terrestrial (Suwannee River, U.S.) and microbial sources (Pony Lake, Antarctica) of DOM were able to sensitize aldrin loss in ice. Scavengers of singlet oxygen, such as furfuryl alcohol and β-carotene, were also added to DOM solutions. Based on the type of organic matter present, the scavengers had different effects on the photochemical degradation of aldrin. Our results indicate that natural organic matter present in ice is an important component of ice photochemical processes.

  16. Thermodynamics of uranium/organic matter interactions in hydrothermal systems

    NASA Astrophysics Data System (ADS)

    Richard, L.

    2003-04-01

    Organic matter is commonly encountered in and around uranium and other ore deposits, which raises the question of the role played by organic compounds in the formation of these deposits (Landais and Gize, 1997). One of the best known examples is the observation of uraninite crystals entrapped within solid bitumens in the Oklo natural reactors. This observation led Nagy et al. (1991) to propose that a liquid, aliphatic-rich bitumen may have acted as a reductant to precipitate uraninite from hydrothermal solutions according to the reaction VIUO2+2(aq)+H_2O(l)=IVUO2(c)+2H^+(aq)+0.5 O2(g). The liquid bitumen was simultaneously oxidized into a polyaromatic solid, which may be represented by the reaction 2.7n- C20H42(l) + 17.85 O2(g) = C54H42(c)+35.7 H_2O(l) where n-C20H42(l) denotes n-eicosane present in the liquid bitumen, and C54H42(c) represents an idealized polyaromatic solid. Recent advances in theoretical organic geochemistry made it possible to generate a comprehensive thermodynamic database for hundreds of crystalline, liquid, gas and aqueous organic compounds of geochemical interest (Shock and Helgeson, 1990; Shock, 1995; Amend and Helgeson, 1997; Helgeson et al., 1998; Richard and Helgeson, 1998; Richard, 2001), which can be used together with thermodynamic properties for uranium-bearing minerals and aqueous species (Grenthe et al., 1992; Shock et al., 1997) to characterize uranium/organic matter interactions in hydrothermal systems as a function of temperature, pressure, oxygen fugacity, and organic matter composition. Activity-fO_2 diagrams have been constructed at a series of temperatures and pressures to investigate possible genetic relationships between uranium mineralizations and solid bitumens of various compositions.

  17. Particulate organic matter distribution along the lower Amazon River: addressing aquatic ecology concepts using fatty acids.

    PubMed

    Mortillaro, Jean-Michel; Rigal, François; Rybarczyk, Hervé; Bernardes, Marcelo; Abril, Gwenaël; Meziane, Tarik

    2012-01-01

    One of the greatest challenges in understanding the Amazon basin functioning is to ascertain the role played by floodplains in the organic matter (OM) cycle, crucial for a large spectrum of ecological mechanisms. Fatty acids (FAs) were combined with environmental descriptors and analyzed through multivariate and spatial tools (asymmetric eigenvector maps, AEM and principal coordinates of neighbor matrices, PCNM). This challenge allowed investigating the distribution of suspended particulate organic matter (SPOM), in order to trace its seasonal origin and quality, along a 800 km section of the Amazon river-floodplain system. Statistical analysis confirmed that large amounts of saturated FAs (15:0, 18:0, 24:0, 25:0 and 26:0), an indication of refractory OM, were concomitantly recorded with high pCO(2) in rivers, during the high water season (HW). Contrastingly, FAs marker which may be attributed in this ecosystem to aquatic plants (18:2ω6 and 18:3ω3) and cyanobacteria (16:1ω7), were correlated with higher O(2), chlorophyll a and pheopigments in floodplains, due to a high primary production during low waters (LW). Decreasing concentrations of unsaturated FAs, that characterize labile OM, were recorded during HW, from upstream to downstream. Furthermore, using PCNM and AEM spatial methods, FAs compositions of SPOM displayed an upstream-downstream gradient during HW, which was attributed to OM retention and the extent of flooded forest in floodplains. Discrimination of OM quality between the Amazon River and floodplains corroborate higher autotrophic production in the latter and transfer of OM to rivers at LW season. Together, these gradients demonstrate the validity of FAs as predictors of spatial and temporal changes in OM quality. These spatial and temporal trends are explained by 1) downstream change in landscape morphology as predicted by the River Continuum Concept; 2) enhanced primary production during LW when the water level decreased and its residence time

  18. Particulate Organic Matter Distribution along the Lower Amazon River: Addressing Aquatic Ecology Concepts Using Fatty Acids

    PubMed Central

    Mortillaro, Jean-Michel; Rigal, François; Rybarczyk, Hervé; Bernardes, Marcelo; Abril, Gwenaël; Meziane, Tarik

    2012-01-01

    One of the greatest challenges in understanding the Amazon basin functioning is to ascertain the role played by floodplains in the organic matter (OM) cycle, crucial for a large spectrum of ecological mechanisms. Fatty acids (FAs) were combined with environmental descriptors and analyzed through multivariate and spatial tools (asymmetric eigenvector maps, AEM and principal coordinates of neighbor matrices, PCNM). This challenge allowed investigating the distribution of suspended particulate organic matter (SPOM), in order to trace its seasonal origin and quality, along a 800 km section of the Amazon river-floodplain system. Statistical analysis confirmed that large amounts of saturated FAs (15:0, 18:0, 24:0, 25:0 and 26:0), an indication of refractory OM, were concomitantly recorded with high pCO2 in rivers, during the high water season (HW). Contrastingly, FAs marker which may be attributed in this ecosystem to aquatic plants (18:2ω6 and 18:3ω3) and cyanobacteria (16:1ω7), were correlated with higher O2, chlorophyll a and pheopigments in floodplains, due to a high primary production during low waters (LW). Decreasing concentrations of unsaturated FAs, that characterize labile OM, were recorded during HW, from upstream to downstream. Furthermore, using PCNM and AEM spatial methods, FAs compositions of SPOM displayed an upstream-downstream gradient during HW, which was attributed to OM retention and the extent of flooded forest in floodplains. Discrimination of OM quality between the Amazon River and floodplains corroborate higher autotrophic production in the latter and transfer of OM to rivers at LW season. Together, these gradients demonstrate the validity of FAs as predictors of spatial and temporal changes in OM quality. These spatial and temporal trends are explained by 1) downstream change in landscape morphology as predicted by the River Continuum Concept; 2) enhanced primary production during LW when the water level decreased and its residence time

  19. Laboratory experimental simulations: Chemical evolution of the organic matter from interstellar and cometary ice analogs

    NASA Astrophysics Data System (ADS)

    Abou Mrad, N.; Vinogradoff, V.; Duverney, F.; Danger, G.; Theulé, P.; Borget, F.; Chiavassa, T.

    2015-01-01

    This contribution addresses the different approaches that are developed in our laboratory to study the chemical evolution of organic matter in stellar or interplanetary environments. In the first approach, starting from interstellar or cometary ice analogs subjected to different energy processes (thermal, photochemical), we aim to explain the mechanism of formation of key molecules (RING project: Reactivity in INterstellar ice Grains) such as HMT, POM or amino acid precursors that are or may be detected in future space missions. In a second approach, we are interested in the detection of volatile molecules sublimating from ice analogs when these latter are heated and/or irradiated (VAHIIA project: Volatile Analysis from the Heating of Interstellar Ice Analogs) through an online experimental device coupling the simulation chamber where ices are formed to a GC-MS instrument. The objective is thus to simulate the effects of the ice material warming when a young star forms or when a comet becomes active. This project provides an inventory of molecules that can be found in hot corinos or in the gaseous phase of comets. In a third approach, we analyze the organic matter contained in the refractory residues that can be considered as cometary analogs (RAHIIA Project: Residue Analysis from the Heating of Interstellar Ice Analogs) using very high resolution mass spectrometry (VHRMS). The results of these analyses show that residues present an important molecular diversity. This technique gives also the possibility to determine the elementary composition of these residues that can be compared to the meteorite composition. These residues can then be a basic material to develop, in a specific planetary environment, a prebiotic chemistry.

  20. Particulate organic matter distribution along the lower Amazon River: addressing aquatic ecology concepts using fatty acids.

    PubMed

    Mortillaro, Jean-Michel; Rigal, François; Rybarczyk, Hervé; Bernardes, Marcelo; Abril, Gwenaël; Meziane, Tarik

    2012-01-01

    One of the greatest challenges in understanding the Amazon basin functioning is to ascertain the role played by floodplains in the organic matter (OM) cycle, crucial for a large spectrum of ecological mechanisms. Fatty acids (FAs) were combined with environmental descriptors and analyzed through multivariate and spatial tools (asymmetric eigenvector maps, AEM and principal coordinates of neighbor matrices, PCNM). This challenge allowed investigating the distribution of suspended particulate organic matter (SPOM), in order to trace its seasonal origin and quality, along a 800 km section of the Amazon river-floodplain system. Statistical analysis confirmed that large amounts of saturated FAs (15:0, 18:0, 24:0, 25:0 and 26:0), an indication of refractory OM, were concomitantly recorded with high pCO(2) in rivers, during the high water season (HW). Contrastingly, FAs marker which may be attributed in this ecosystem to aquatic plants (18:2ω6 and 18:3ω3) and cyanobacteria (16:1ω7), were correlated with higher O(2), chlorophyll a and pheopigments in floodplains, due to a high primary production during low waters (LW). Decreasing concentrations of unsaturated FAs, that characterize labile OM, were recorded during HW, from upstream to downstream. Furthermore, using PCNM and AEM spatial methods, FAs compositions of SPOM displayed an upstream-downstream gradient during HW, which was attributed to OM retention and the extent of flooded forest in floodplains. Discrimination of OM quality between the Amazon River and floodplains corroborate higher autotrophic production in the latter and transfer of OM to rivers at LW season. Together, these gradients demonstrate the validity of FAs as predictors of spatial and temporal changes in OM quality. These spatial and temporal trends are explained by 1) downstream change in landscape morphology as predicted by the River Continuum Concept; 2) enhanced primary production during LW when the water level decreased and its residence time

  1. Xiphinema americanum as Affected by Soil Organic Matter and Porosity.

    PubMed

    Ponchillia, P E

    1972-07-01

    The effects of four soil types, soil porosity, particle size, and organic matter were tested on survival and migration of Xiphinema americanum. Survival and migration were significantly greater in silt loam than in clay loam and silty clay soils. Nematode numbers were significantly greater in softs planted with soybeans than in fallow softs. Nematode survival was greatest at the higher of two pore space levels in four softs. Migration of X. americanum through soft particle size fractions of 75-150, 150-250, 250-500, 500-700, and 700-1,000 mu was significantly greater in the middle three fractions, with the least occurring in the smallest fraction. Additions of muck to silt loam and loamy sand soils resulted in reductions in survival and migration of the nematode. The fulvic acid fraction of muck, extracted with sodium hydroxide, had a deleterious effect on nematode activity. I conclude that soils with small amounts of air-filled pore space, extremes in pore size, or high organic matter content are deleterious to the migration and survival of X. americanum, and that a naturally occurring toxin affecting this species may be present in native soft organic matter.

  2. Temperature sensitivity of organic-matter decay in tidal marshes

    USGS Publications Warehouse

    Kirwan, Matthew L.; Guntenspergen, Glenn R.; Langley, J.A.

    2014-01-01

    Approximately half of marine carbon sequestration takes place in coastal wetlands, including tidal marshes, where organic matter contributes to soil elevation and ecosystem persistence in the face of sea-level rise. The long-term viability of marshes and their carbon pools depends, in part, on how the balance between productivity and decay responds to climate change. Here, we report the sensitivity of labile soil organic-matter decay in tidal marshes to seasonal and latitudinal variations in temperature measured over a 3-year period. We find a moderate increase in decay rate at warmer temperatures (3-6% per °C, Q10 = 1.3-1.5). Despite the profound differences between microbial metabolism in wetlands and uplands, our results indicate a strong conservation of temperature sensitivity. Moreover, simple comparisons with organic-matter production suggest that elevated atmospheric CO2 and warmer temperatures will accelerate carbon accumulation in marsh soils, and potentially enhance their ability to survive sea-level rise.

  3. Matrix protected organic matter in a river dominated margin: A possible mechanism to sequester terrestrial organic matter?

    NASA Astrophysics Data System (ADS)

    Mead, Ralph N.; Goñi, Miguel A.

    2008-06-01

    The provenance of organic matter in surface sediments from the northern Gulf of Mexico was investigated by analyzing the compositions of lipid biomarkers ( n-alkanes, fatty acids, sterols) liberated after a series of chemical treatments designed to remove different organo-mineral matrix associations (i.e. freely extractable, base-hydrolyzable, unhydrolyzable). Bulk analyses of the organic matter (carbon content, carbon:nitrogen ratios, stable and radiocarbon isotopic analyses) were also performed on the intact sediments and their non-hydrolyzable, demineralized residue. We found recognizable lipids from distinct sources, including terrestrial vascular plants, bacteria and marine algae and zooplankton, within each of the isolated fractions. Based on the lipid signatures and bulk compositions, the organic matter within the unhydrolyzable fractions appeared to be the most diagenetically altered, was the oldest in age, and had the highest abundance of terrigenous lipids. In contrast, the base-hydrolyzable fraction was the most diagentically unaltered, had the youngest ages and was most enriched in N and marine lipids. Our results indicate that fresh, autochthonous organic matter is the most important contributor to base-hydrolyzable lipids, whereas highly altered allochthonous sources appear to be predominant source of unhydrolyzable lipids in the surface sediments from the Atchafalaya River shelf. Overall, the lipid biomarker signatures of intact sediments were biased towards the autochthonous source because many of the organic compounds indicative of degraded, terrigenous sources were protected from extraction and saponification by organo-mineral matrices. It is only after these protective matrices were removed by treatment with HCl and HF that these compounds became evident.

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

    NASA Technical Reports Server (NTRS)

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

    1972-01-01

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

  5. Comments on D/H ratios in chondritic organic matter

    NASA Astrophysics Data System (ADS)

    Smith, J. W.; Rigby, D.

    1981-06-01

    D/H ratios in chondritic organic matter are investigated. Demineralized organic residues obtained from previous experiments were dried in a quartz reaction vessel under vacuum for 60 minutes at 250-300 C and then combusted in oxygen for 20 minutes at 850 C. The apparatus is described and the results of the experiments such as D/H ratios in water and measurements on total carbon dioxide are given. Atomic H/C ratios calculated directly from the quantities of carbon dioxide and water recovered, are reported according to Standard Mean Ocean Water and Pee Dee Belemnite, using the customary notation.

  6. Organic matter in meteorites and comets - Possible origins

    NASA Technical Reports Server (NTRS)

    Anders, Edward

    1991-01-01

    At least six extraterrestrial environments may have contributed organic compounds to meteorites and comets: solar nebula, giant-planet subnebulae, asteroid interiors containing liquid water, carbon star atmospheres, and diffuse or dark interstellar clouds. The record in meteorites is partly obscured by pervasive reheating that transformed much of the organic matter to kerogen; nonetheless, it seems that all six formation sites contributed. For comets, the large abundance of HCHO, HCN, and unsaturated hydrocarbons suggests an interstellar component of 50 percent or more, but the contributions of various interstellar processes, and of a solar-nebula component, are hard to quantify. A research program is outlined that may help reduce these uncertainties.

  7. [The refractory susceptibility in determination of sulfur in organic drugs using the Schoniger method].

    PubMed

    Listov, S A; Arsamastsev, A P; Gamanina, G J

    1988-10-01

    Conventional methods of the determination of sulphur in organic drugs were studied (Schöniger method) and new methods developed. Emphasis was put on the disturbance effect of 5 elements, which often occur in the structure of organic drug compounds. It could be shown, that the disturbance effect of nitrogen and chlorine was overcome by the use of carbamide and ammonium carbonate in the absorption solution. The effect of fluorine was abolished by the use of boric acid and a special two-spiral technique of the analysis. Based on these studies concrete recommendations for the Schöniger method of sulphur determination in drugs of various composition of elements were given. PMID:3212013

  8. [The refractory susceptibility in determination of sulfur in organic drugs using the Schoniger method].

    PubMed

    Listov, S A; Arsamastsev, A P; Gamanina, G J

    1988-10-01

    Conventional methods of the determination of sulphur in organic drugs were studied (Schöniger method) and new methods developed. Emphasis was put on the disturbance effect of 5 elements, which often occur in the structure of organic drug compounds. It could be shown, that the disturbance effect of nitrogen and chlorine was overcome by the use of carbamide and ammonium carbonate in the absorption solution. The effect of fluorine was abolished by the use of boric acid and a special two-spiral technique of the analysis. Based on these studies concrete recommendations for the Schöniger method of sulphur determination in drugs of various composition of elements were given.

  9. Flood Pulse Influence on Export of Terrestrial Organic Matter

    NASA Astrophysics Data System (ADS)

    Dalzell, B. J.; Harbor, J. M.; Filley, T. R.

    2004-12-01

    While much attention has been placed on characterizing Terrestrial Organic Matter (TOM) export from large rivers, recent research has shown that in-stream processing of TOM in smaller streams and rivers over shorter time scales can be an important upland component of regional carbon budgets not detected at the outlets of large rivers. With predictions of climate change accompanied by more intense rainfall patterns in some areas, it is important to understand the linkage between flood events and watershed export of TOM. To this end, we have collected water samples from Big Pine Creek watershed, an 850km2 watershed located in west central Indiana. Organic carbon in dissolved, colloidal, and particulate size fractions has been described with molecular and stable carbon isotope techniques to track source, quantity, and compositional changes of TOM over changing flow conditions. Results from these samples show that flood conditions export dramatically more TOM; not only from increases in discharge, but also from increases in concentration of terrestrial organic carbon to all size fractions. While molecular biomarkers show increases in terrestrial organic matter, bulk stable carbon isotope values show that the sources of TOM do not remain constant. Rather, relative contributions from C4 plants (corn in this study area) increase during flood conditions by up to 40 percent. Finally, increases in rainfall intensity are likely to disproportionately increase organic carbon export from terrestrial systems, especially from smaller watersheds where short duration and high intensity flow events dominate annual discharge.

  10. Why dissolved organic matter (DOM) enhances photodegradation of methylmercury

    SciTech Connect

    Qian, Yun; Yin, Xiangping Lisa; Brooks, Scott C; Liang, Liyuan; Gu, Baohua

    2014-01-01

    Methylmercury (MeHg) is known to degrade photochemically, but it remains unclear what roles naturally dissolved organic matter (DOM) and complexing organic ligands play in MeHg photodegradation. Here we investigate the rates and mechanisms of MeHg photodegradation using DOM samples with varying oxidation states and origins as well as organic ligands with known molecular structures. All DOM and organic ligands increased MeHg photodegradation under solar irradiation, but the first-order rate constants varied depending on the oxidation state of DOM and the type and concentration of the ligands. Compounds containing both thiols and aromatics (e.g., thiosalicylate and reduced DOM) increased MeHg degradation rates far greater than those containing only aromatic or thiol functional groups (e.g., salicylate or glutathione). Our results suggest that, among other factors, the synergistic effects of thiolate and aromatic moieties in DOM greatly enhance MeHg photodegradation.

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

    EPA Science Inventory

    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...

  12. Spectrometric characterization of effluent organic matter of a sequencing batch reactor operated at three sludge retention times.

    PubMed

    Esparza-Soto, M; Núñez-Hernández, S; Fall, C

    2011-12-01

    Effluent organic matter (EfOM) from activated sludge systems is composed primarily of influent refractory compounds, residual degradable substrate, intermediate products and soluble microbial products (SMPs). Depending on operational conditions (hydraulic and sludge retention time (SRT)), the quantity and quality of EfOM significantly changes. The main objective of this research was to quantify and characterize the EfOM of a lab-scale activated sludge sequencing batch reactor (SBR), which was operated at three SRTs and fed glucose, an easily biodegradable substrate. EfOM was followed with two direct-quantification methods (chemical oxygen demand (COD) and dissolved organic carbon (DOC)), three spectrometric methods (ultraviolet absorbance at 254 nm (UVA(254)), excitation-emission matrix (EEM) fluorescence and parallel factor analysis (PARAFAC)) and three organic matter (OM) indices (specific UVA(254) (SUVA), SUVA-COD, COD/DOC ratio). The significant increment of UVA(254) and OM indices after treatment indicated an accumulation of refractory high-molecular-weight humic-like compounds in the EfOM, which demonstrated that EfOM was composed mainly by SMPs and not glucose. On the other hand, as the SRT increased, the amount of EfOM decreased, but SUVA, SUVA-COD and fluorescence intensity increased; these trends indicated the accumulation of SMPs of increased molecular weight and aromaticity. Increasing SRT in the SBRs reduced the amount of EfOM, but increased its aromaticity and reactivity. Visual analysis of EfOM EEMs showed two protein- and one humic-like peak, which were attributed to SMPs generated within the SBRs. PARAFAC determined that a two-component model best represented EfOM EEMs. The two-components from PARAFAC were mathematically correlated to the visually identified protein- and humic-like SMPs peaks.

  13. Soil Quality of Restinga Forest: Organic Matter and Aluminum Saturation

    NASA Astrophysics Data System (ADS)

    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.

  14. Organic matter recycling in a shallow coastal zone (NW Mediterranean): The influence of local and global climatic forcing and organic matter lability on hydrolytic enzyme activity

    NASA Astrophysics Data System (ADS)

    Misic, Cristina; Harriague, Anabella Covazzi

    2008-12-01

    Seawater and sediment were collected on a monthly basis from a shallow (10.5 m depth) coastal site in the Ligurian Sea (NW Mediterranean) from November 1993 to December 1994 to determine the main environmental forces that influenced the biogeochemical processes and to study the relationships between the availability and lability of the organic matter (OM) and hydrolytic enzymatic activity. The current direction throughout the sampling year was influenced by the climatic conditions, which showed significant correlations with north atlantic oscillation (NAO) index values. The current generally flowed northwards in spring. This could cause significantly lower transparency values than in the summer, when an eastward current probably reduced the allochthonous input of material from the main local watercourse and contributed to turning the conditions from mesotrophic to oligotrophic. Spring and summer were separated by transitional periods more than by the canonical autumn and winter seasons. These transitions were characterised by a reduction in salinity values and by resuspension caused by water column mixing and a current flowing towards the southwest. The significant inverse correlations of the chlorophyll- a and protein concentrations, bacterial abundance and proteolysis of the bottom seawater and transparency showed the direct influence of resuspension on the organic matter dynamics. Moreover, OM trophic quality influenced the bacterial parameters and the enzymatic activities. The glycolytic β glucosidase and chitinase activities and their bacterial cell-specific hydrolytic rates were higher when substrates such as hydrolysable proteins were available, while they decreased when refractory compounds were abundant. The low leucine aminopeptidase: β glucosidase ratio values observed in the water column were presumably related to the potential ease with which microbes obtained protein-derived materials and energy, the protein hydrolysable fraction being estimated at

  15. Using Riverine Natural Organic Matter to Test the Hypothesis that Soil Organic Matter is Modified by Contact with Sodium Hydroxide

    NASA Astrophysics Data System (ADS)

    Perdue, E. Michael; Driver, Shamus; Hertkorn, Norbert; Harir, Mourad; Schmitt-Kopplin, Philippe

    2016-04-01

    It has been postulated by some scientists that soil humic acids and fulvic acids are an artifact of alkaline extractions of soil. Riverine natural organic matter (NOM) is obtained in part by dissolution and transport of organic matter from soils by meteoric waters at acidic to circumneutral pH. The NOM may be fractionated into humic acid (HA), fulvic acid (FA), and hydrophilic NOM by adsorption of HA and FA onto XAD-8 resin at pH < 2, followed by their desorption with NaOH at pH 13. Alternatively, riverine NOM may be concentrated using reverse osmosis (RO) and desalted by cation exchange. Several properties of Suwannee River NOM prior to its isolation, after concentration by RO, and after the XAD-8 process are compared to detect modifications that might have resulted from exposure of the sample to low and high pH.

  16. The composition and degradability of upland dissolved organic matter

    NASA Astrophysics Data System (ADS)

    Moody, Catherine; Worrall, Fred; Clay, Gareth

    2016-04-01

    In order to assess controls on the degradability of DOM in stream water, samples of dissolved organic matter (DOM) and particulate organic matter (POM) were collected every month for a period of 24 months from an upland, peat-covered catchment in northern England. Each month the degradability of the DOM was assessed by exposing river water to light for up to 24 hours, and the change in the dissolved organic carbon (DOC) concentration in the water was measured. To provide context for the analysis of DOM and its degradability, samples of peat, vegetation, and litter were also taken from the same catchment and analysed. The organic matter samples were analysed by several methods including: elemental analysis (CHN and O), bomb calorimetry, thermogravimetric analysis, pyrolysis GC/MS, ICP-OES, stable isotope analysis (13C and 15N) and 13C solid state nuclear magnetic resonance (NMR). The water samples were analysed for pH, conductivity, absorbance at 400nm, anions, cations, particulate organic carbon (POC) and DOC concentrations. River flow conditions and meteorology were also recorded at the site and included in the analysis of the composition and degradability of DOM. The results of multiple regression models showed that the rates of DOC degradation were affected by the N-alkyl, O-alkyl, aldehyde and aromatic relative intensities, gross heat, OR and C:N. Of these, the N-alkyl relative intensity had the greatest influence, and this in turn was found to be dependent on the rainfall and soil temperature in the week before sampling.

  17. Isotopic constraints on the origin of meteoritic organic matter

    NASA Technical Reports Server (NTRS)

    Kerridge, J. F.

    1991-01-01

    Salient features of the isotopic distribution of H, C and N in the organic material found in carbonaceous meteorites are noted. Most organic fractions are strongly enriched in D with respect to the D/H ratio characteristic of H2 in the protosolar system; substantial variations in C-13/C-12 ratio are found among different molecular species, with oxidised species tending to be C-13 enriched relative to reduced species; some homologous series reveal systematic decrease in C-13/C-12 with increasing C number; considerable variation in N-15/N-14 ratio is observed within organic matter, though no systematic pattern to its distribution has yet emerged; no interelement correlations have been observed between isotope enrichments for the different biogenic elements. The isotopic complexity echoes the molecular diversity observed in meteoritic organic matter and suggests that the organic matter was formed by multiple processes and/or from multiple sources. However, existence of a few systematic patterns points towards survival of isotopic signatures characteristic of one or more specific processes. The widespread D enrichment implies either survival of many species of interstellar molecule or synthesis from a reservoir containing a significant interstellar component. Several of the questions raised above can be addressed by more detailed determination of the distribution of the H, C and N isotopes among different well-characterized molecular fractions. Thus, the present study is aimed at discovering whether the different amino acids have comparable D enrichments, which would imply local synthesis from a D-enriched reservoir, or very viable D enrichments, which would imply survival of some interstellar amino acids. The same approach is also being applied to polycyclic aromatic hydrocarbons. Because the analytical technique employed (secondary ion mass spectrometry) can acquire data for all three isotopic systems from each molecular fraction, any presently obscured interelement

  18. Soil organic matter regulates molybdenum storage and mobility in forests

    USGS Publications Warehouse

    Marks, Jade A; Perakis, Steven; King, Elizabeth K; Pett-Ridge, Julie

    2015-01-01

    The trace element molybdenum (Mo) is essential to a suite of nitrogen (N) cycling processes in ecosystems, but there is limited information on its distribution within soils and relationship to plant and bedrock pools. We examined soil, bedrock, and plant Mo variation across 24 forests spanning wide soil pH gradients on both basaltic and sedimentary lithologies in the Oregon Coast Range. We found that the oxidizable organic fraction of surface mineral soil accounted for an average of 33 %of bulk soil Mo across all sites, followed by 1.4 % associated with reducible Fe, Al, and Mn-oxides, and 1.4 % in exchangeable ion form. Exchangeable Mo was greatest at low pH, and its positive correlation with soil carbon (C) suggests organic matter as the source of readily exchangeable Mo. Molybdenum accumulation integrated over soil profiles to 1 m depth (τMoNb) increased with soil C, indicating that soil organic matter regulates long-term Mo retention and loss from soil. Foliar Mo concentrations displayed no relationship with bulk soil Mo, and were not correlated with organic horizon Mo or soil extractable Mo, suggesting active plant regulation of Mo uptake and/or poor fidelity of extractable pools to bioavailability. We estimate from precipitation sampling that atmospheric deposition supplies, on average, over 10 times more Mo annually than does litterfall to soil. In contrast, bedrock lithology had negligible effects on foliar and soil Mo concentrations and on Mo distribution among soil fractions. We conclude that atmospheric inputs may be a significant source of Mo to forest ecosystems, and that strong Mo retention by soil organic matter limits ecosystem Mo loss via dissolution and leaching pathways.

  19. Differences in spectroscopic characteristics between dissolved and particulate organic matters in sediments: Insight into distribution behavior of sediment organic matter.

    PubMed

    He, Wei; Jung, Heonjae; Lee, Jong-Hyun; Hur, Jin

    2016-03-15

    In this study, we examined the distribution behavior of sediment organic matter (SOM) between dissolved and particulate phases and the potential influencing factors by comparing the spectroscopic features of pore water organic matter (PWOM) and alkaline-extractable organic matter (AEOM) of river sediments. The characteristics of SOM were described by several selected spectral indicators and fluorescence excitation emission matrix (EEM)-parallel factor analysis (PARAFAC). The spectral indicators showed that larger sized SOM molecules with a higher aromatic content were more enriched in sediment particles than in pore water. The relative ratios of humification index between dissolved and particulate phases revealed that the SOM constituents with a higher degree of structural condensation were preferentially distributed onto sediment particles. EEM-PARAFAC demonstrated different distribution behaviors of protein-like (tyrosine-like and tryptophan-like) and humic-like substances in sediments. The relative abundance of tyrosine-like component was much higher in PWOM than in AEOM, whereas the other three components tended to be more abundant in AEOM. The predominant presence of tyrosine-like component suggests its potential operation as a discriminant indicator between PWOM and AEOM. Spearman correlations and non-metric multidimensional scaling further revealed that distribution of protein-like components onto sediment particles might be associated with reductive environments, aluminum minerals, and anthropogenic activities of upstream watersheds. This study demonstrated a successful application of using EEM-PARAFAC to examine the distribution behavior of different SOM constitutes between dissolved and solid phases.

  20. Bulk organic matter and nitrogen removal from reclaimed water during groundwater recharge by enhanced direct injection well.

    PubMed

    Xuan, Zhao; Meng, Zhang; Xuzhou, Cheng

    2009-01-01

    Water shortages lead to increasing attention to artificial groundwater recharge by reclaimed water. A new kind of approach, enhanced direct injection-well recharge (EnDir) consisting of short- and long-term soil treatment, is considered to be suitable for large cities in China. In this paper, EnDir was simulated by soil columns in the laboratory with the secondary effluent as raw water that was ozonated before EnDir. Laboratory-scale experiments demonstrate that the short-term part of EnDir can remove 47 to 60% dissolved organic carbon (DOC), convert 5 mg/L of ammonia-nitrogen to equivalent nitrate-nitrogen, and offer preferred removal of non-UV-absorbing organics. Soluble microbial byproducts and fulvic-acid-like materials can be ozonated and then partially biodegraded. The residuals of organic matter as a refractory fraction are biodegraded continuously during the long-term part. The DOC value of 1.8 to 2.5 mg/L can be reached, and 40% of organic matter with molecular weight less than 500 Da can be removed after full-term EnDir. PMID:19280901

  1. Comprehensive assessment of precursors, diagenesis, and reactivity to water treatment of dissolved and colloidal organic matter

    USGS Publications Warehouse

    Leenheer, J.A.

    2004-01-01

    A comprehensive isolation, fractionation, and characterization research approach was developed for dissolved and colloidal organic matter (DOM) in water, and it was applied to various surface- and groundwaters to assess DOM precursors, DOM diagenesis, and DOM reactivity to water treatment processes. Major precursors for natural DOM are amino sugars, condensed tannins, and terpenoids. Amino sugar colloids derived from bacterial cell walls are incompletely removed by drinking water treatment and foul reverse osmosis membranes, but are nearly quantitatively removed by soil/aquifer treatment. When chlorinated, amino sugars produce low yields of regulated disinfection by-products (DBFs) but they produce significant chlorine demand that is likely caused by chlorination of free amino groups. Condensed tannins are major precursors for "blackwater" DOM such as that found in the Suwannee River. This DOM produces high yields of DBPs upon chorination, and is efficiently removed by coagulation/flocculation treatment. Terpenoid-derived DOM appears to be biologically refractory, infiltrates readily into groundwater with little removal by soil/aquifer treatment, gives low DBF-yields upon chlorination and is poorly removed by coagulation/flocculation treatments. Peptides derived from proteins are major components of the base DOM fraction (10% or less of the mass of DOM), and this fraction produces large yields of haloacetonitriles upon chorination.

  2. Organic matter oxidation and aragonite diagenesis in a coral reef

    SciTech Connect

    Tribble, G.W. Univ. of Hawaii, Honolulu )

    1993-05-01

    A combination of field and theoretical work is used to study controls on the saturation state of aragonite inside a coral-reef framework. A closed-system ion-speciation model is used to evaluate the effect of organic-matter oxidation on the saturation state of aragonite. The aragonite saturation state initially drops below 1 but becomes oversaturated during sulfate reduction. The C:N ratio of the organic matter affects the degree of oversaturation with N-poor organic material resulting in a system more corrosive to aragonite. Precipitation of sulfide as FeS strongly affects the aragonite saturation state, and systems with much FeS formation will have a stronger tendency to become oversaturated with respect to aragonite. Both precipitation and dissolution of aragonite are predicted at different stages of the organic reaction pathway if the model system is maintained at aragonite saturation. Field data from a coral-reef framework indicate that the system maintains itself at aragonite saturation, and model-predicted changes in dissolved calcium follow those observed in the interstitial waters of the reef. Aragonite probably acts as a solid-phase buffer in regulating the pH of interstitial waters. Because interstitial water in the reef has a short residence time, the observed equilibration suggests rapid kinetics.

  3. Organic matter and nutrient inputs to the Humber Estuary, England.

    PubMed

    Boyes, Suzanne; Elliott, Michael

    2006-01-01

    Estuaries are sinks for organic matter and nutrients entering both from their catchments and also from the adjacent lands and urban areas and in turn they are sources of such materials to the adjacent coast. The present paper quantifies the relative amounts of natural and anthropogenic organic matter and nutrients entering the Humber Estuary, Eastern England, including the allochthonous and autochthonous materials, those from urban and industrial sewage and from the catchment drainage of arable land. These data thus give a budget for the estuary which in turn answers questions fundamental to the management of the estuary. The estimations within the study have been carried out against a background of designating estuaries under the European Union Urban Waste-water Treatment Directive and the EU Nitrates Directive. The assessment has particularly addressed the question, related to the former Directive, of whether the Humber Estuary is eutrophic or likely to become eutrophic unless management measures are taken. Thus the paper indicates the nature and value of control measures such as treatment plant upgrading and the designation of Nitrate Vulnerable Zones. The paper includes the recent national and European discussions on the designation of areas under these Directives. Finally, the study has allowed a quantification of the present organic inputs to the estuary in comparison to those entering prior to large scale land-claim which had removed natural organic-producing wetlands.

  4. Remote monitoring of organic matter in the ocean

    NASA Astrophysics Data System (ADS)

    Niccolai, Filippo; Bazzani, Marco; Cecchi, Giovanna; Innamorati, Mario; Massi, Luca; Nuccio, Caterina; Santoleri, Rosalia

    1999-12-01

    The monitoring of organic matter, suspended or dissolved in the water column, is relevant for the study of the aquatic environment. Actually, the Dissolved Organic Matter (DOM) represents a major reservoir of reactive carbon in the global carbon cycle, thus influencing significantly the marine ecosystem. Due to the strong absorption in the near ultraviolet, DOM reduces considerably the extinction path of solar light in the water column, affecting phytoplankton population and its vertical distribution. The measurement of the DOM absorption coefficient has to be regarded as a good parameter for the monitoring of water quality. This paper deals with the measurements carried out during the oceanographic campaign 'Marine Fronts,' which took place in the Western Mediterranean Sea and Atlantic Ocean from July 14 to August 5, 1998. In this measurement campaign, a high spectral resolution fluorescence lidar (FLIDAR) was installed on the rear-deck of the O/V 'Urania,' acquiring remote fluorescence spectra both in ship motion and in stations. A particular attention was devoted to the monitoring of DOM distribution in the different water masses in marine frontal areas. The lidar data were compared and integrated with SST satellite data and biological samplings. The results show that FLIDAR data agree with satellite imagery, particularly for marine front detection. The comparison with water sample data gave indications for retrieving the DOM absorption coefficient directly from fluorescence remote spectra. In addition, a protein like fluorescence band was detected in the measurements carried out on total suspended matter filtered from the water samplings.

  5. Organic speciation of size-segregated atmospheric particulate matter

    NASA Astrophysics Data System (ADS)

    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

  6. Photochemical production of singlet oxygen from particulate organic matter.

    PubMed

    Appiani, Elena; McNeill, Kristopher

    2015-03-17

    Dissolved organic matter is established as one of the most relevant photosensitizers in aquatic environments, producing singlet oxygen (1O2) alongside other photochemically produced reactive intermediates. While the production of 1O2 from DOM has been well studied, the relative importance of particulate organic matter (POM) to the overall 1O2 production is less well understood. POM is known to play an important role in pollutant fate through the sorption and transport of hydrophobic pollutants. If POM is directly involved in 1O2 production, sorbed molecules would be expected to undergo enhanced photodegradation. In this work, synthetic POM was prepared by coating silica particles with commercial humic acid. The photochemical behavior of these POM samples was compared to dissolved commercial humic acids (DOM). Suspended natural sediment was also studied to test the environmental relevance of the synthetic POM model. Synthetic POM particles appear to simulate well the 1O2-production of suspended sediment. The 1O2 concentrations experienced by POM-sorbed probe molecules was up to 30% higher than experienced by DOM-sorbed ones, even though the aqueous concentration of 1O2 in irradiated POM suspensions was much lower than the analogous DOM solutions. These results were interpreted with a reaction-diffusion model, which suggested that the production rate of 1O2 by POM is lower than DOM, but the loss of 1O2 from the POM-phase is also lower than DOM. Based on the experimental results of this study, calculations were conducted to estimate the impact of removing POM on 1O2-mediated processes. These calculations indicate that compounds with a log Koc value near 4 will be most affected by removal of POM and that the magnitude of the effect is proportional to the fraction of the total organic matter represented by POM. This study demonstrates that particles can play an important role in the degradation of organic compounds via aquatic photochemistry.

  7. Missing links in the root-soil organic matter continuum.

    SciTech Connect

    O'Brien, S. L.; Iversen, C. M.; Biosciences Division; 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 (Fig. 1). 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.

  8. Competitive Sorption and Desorption of Chlorinated Organic Solvents (DNAPLs) in Engineered Natural Organic Matter

    SciTech Connect

    Tang, Jixin; Weber, Walter J., Jr.

    2004-03-31

    The effects of artificially accelerated geochemical condensation and maturation of natural organic matter on the sorption and desorption of trichloroethylene (TCE) and tetrachloroethylene (PCE) were studied. The sorption and desorption of TCE in the presence and absence of the competing PCE and 1,2-dichlorobenzene (DCB) were also examined. A sphagnum peat comprising geologically young organic matter was artificially ''aged'' using superheated water, thus increasing the aromaticity and the degree of condensation of its associated organic matter. The sorption of all solutes tested were increased remarkably and their respective desorptions reduced, by the aged peat. The sorption capacities and isotherm nonlinearities of the peat for both TCE and PCE were found to increase as treatment temperature increased. In the competitive sorption studies, both PCE and DCB were found to depress TCE sorption, with PCE having greater effects than DCB, presumably because the molecular structure o f the former is more similar to that of TCE.

  9. Application of organic geochemistry to detect signatures of organic matter in the Haughton impact structure

    NASA Astrophysics Data System (ADS)

    Parnell, John; Lee, Pascal; Osinski, Gordon R.; Cockell, Charles S.

    2005-12-01

    Organic geochemistry applied to samples of bedrock and surface sediment from the Haughton impact structure detects a range of signatures representing the impact event and the transfer of organic matter from the crater bedrock to its erosion products. The bedrock dolomite contains hydrocarbon-bearing fluid inclusions which were incorporated before the impact event. Comparison of biomarker data from the hydrocarbons in samples inside and outside of the crater show the thermal signature of an impact. The occurrence of hydrocarbon inclusions in hydrothermal mineral samples shows that organic matter was mobilized and migrated in the immediate aftermath of the impact. The hydrocarbon signature was then transferred from bedrock to the crater-fill lacustrine deposits and present-day sediments in the crater, including wind-blown detritus in snow/ice. Separate signatures are detected from modern microbial life in crater rock and sediment samples. Signatures in Haughton crater samples are readily detectable because they include hydrocarbons generated by the burial of organic matter. This type of organic matter is not expected in crater samples on other planets, but the Haughton data show that, using very high resolution detection of organic compounds, any signature of primitive life in the crater rocks could be transferred to surface detritus and so extend the sampling medium.

  10. Modelling of organic matter dynamics during the composting process.

    PubMed

    Zhang, Y; Lashermes, G; Houot, S; Doublet, J; Steyer, J P; Zhu, Y G; Barriuso, E; Garnier, P

    2012-01-01

    Composting urban organic wastes enables the recycling of their organic fraction in agriculture. The objective of this new composting model was to gain a clearer understanding of the dynamics of organic fractions during composting and to predict the final quality of composts. Organic matter was split into different compartments according to its degradability. The nature and size of these compartments were studied using a biochemical fractionation method. The evolution of each compartment and the microbial biomass were simulated, as was the total organic carbon loss corresponding to organic carbon mineralisation into CO(2). Twelve composting experiments from different feedstocks were used to calibrate and validate our model. We obtained a unique set of estimated parameters. Good agreement was achieved between the simulated and experimental results that described the evolution of different organic fractions, with the exception of some compost because of a poor simulation of the cellulosic and soluble pools. The degradation rate of the cellulosic fraction appeared to be highly variable and dependent on the origin of the feedstocks. The initial soluble fraction could contain some degradable and recalcitrant elements that are not easily accessible experimentally. PMID:21978424

  11. Coastal-offshore exchange of organic matter across the Cape Ghir filament (NW Africa) during moderate upwelling

    NASA Astrophysics Data System (ADS)

    Santana-Falcón, Yeray; Benavides, Mar; Sangrà, Pablo; Mason, Evan; Barton, Eric Desmond; Orbi, Abdellatif; Arístegui, Javier

    2016-02-01

    The net coastal-ocean export of particulate organic carbon (POC), dissolved organic carbon (DOC) and chlorophyll a is studied in August 2009 at the Cape Ghir filament, a recurrent feature located within the NW African upwelling system. The estimated flux of excess total organic carbon (the non-refractory pools of DOC and POC) is about 2.1 × 109 kg C y- 1. DOC represents ~ 70% of the excess organic carbon in August 2009, during moderate upwelling. Assuming that this flux is representative of the range within a typical year, the yearly offshore net transport of total organic carbon would represent at least 29% of the primary production in this area. Since the Cape Ghir filament may extend hundreds of kilometers offshore, the associated seaward flux of organic carbon would contribute to the high microbial respiration rates reported from the nearby oligotrophic open ocean region. Our results illustrate that, when considering the regional carbon budgets of eastern boundary regions, it is imperative to take account of the offshore transport of organic matter in the numerous and recurrent upwelling filaments.

  12. Soft X-Ray Photoionizing Organic Matter from Comet Wild 2: Evidence for the Production of Organic Matter by Impact Processes

    NASA Technical Reports Server (NTRS)

    Zolensky, Michael E.; Wirick, S.; Flynn, G. J.; Jacobsen, C.; Na

    2011-01-01

    The Stardust mission collected both mineral and organic matter from Comet Wild 2 [1,2,3,4]. The organic matter discovered in Comet Wild 2 ranges from aromatic hydrocarbons to simple aliphatic chains and is as diverse and complex as organic matter found in carbonaceous chondrites and interplanetary dust particles.[3,5,6,7,8,9]. Compared to insoluble organic matter from carbonaceous chondrites the organic matter in Comet Wild 2 more closely resembles organic matter found in the IDPS both hydrous and anhydrous. Common processes for the formation of organic matter in space include: Fischer-Tropsch, included with this aqueous large body and moderate heating alterations; UV irradiation of ices; and; plasma formation and collisions. The Fischer-Tropsch could only occur on large bodies processes, and the production of organic matter by UV radiation is limited by the penetration depth of UV photons, on the order of a few microns or less for most organic matter, so once organic matter coats the ices it is formed from, the organic production process would stop. Also, the organic matter formed by UV irradiation would, by the nature of the process, be in-sensitive to photodissocation from UV light. The energy of soft X-rays, 280-300 eV occur within the range of extreme ultraviolet photons. During the preliminary examination period we found a particle that nearly completely photoionized when exposed to photons in the energy range 280-310eV. This particle experienced a long exposure time to the soft x-ray beam which caused almost complete mass loss so little chemical information was obtain. During the analysis of our second allocation we have discovered another particle that photoionized at these energies but the exposure time was limited and more chemical information was obtained.

  13. ENVIRONMENTAL RESEARCH BRIEF: CHARACTERIZATION OF ORGANIC MATTER IN SOIL AND AQUIFER SOLIDS

    EPA Science Inventory

    The focus of this work was the evaluation of analytical methods to determine and characterize fractions of subsurface organic matter. Major fractions of total organic carbon (TOC) include: particulate organic carbon (POC) in aquifer material, dissolved organic carbon (DOC) and ...

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

    PubMed

    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.

  15. Organic Matter as an Indicator of Soil Degradation

    NASA Astrophysics Data System (ADS)

    Romero Diaz, Asuncion; Damian Ruiz Sinoga, Jose

    2010-05-01

    Numerous and expensive physical-chemical tests are often carried out to determine the level of soil degration. This study was to find one property, as Organic Matter, which is usually analyzed for determine the soil degradation status. To do this 19 areas in the south and southeast of the Iberian Peninsula (provinces of Málaga, Granada, Almería y Murcia) were selected and a wide sampling process was carried out. Sampling points were spread over a wide pluviometric gradient (from 1100 mm/yr to 232 mm/yr) covering the range from Mediterranean wet to dry. 554 soil surface samples were taken from soil (0-10 cm) and the following properties were analyzed: Texture, Organic Matter (OM), Electric Conductivity (EC), Aggregate Stability (AE) y Cation Exchange Capacity (CEC). These properties were intercorrelated and also with rainfall and the K factor of soil erosion, calculated for each sampling point. Los results obtained by applying the Pearson correlation coefficient to the database shows how as rainfall increases so does OM content (0,97) and la CEC (0,89), but K factor (-0,80) reacts inversely. The content of OM in the soil is related to its biological activity and this in turn is the result of available wáter within the system and, consequently, rainfall. This is specially important in fragile and complex ecogeomorphological systems as is the case of the Mediterranean, where greater or lesser rainfall is similarly reflected in the levels of increase or decrease of soil organic matter. This affirmation is reinforced by linking the organic matter of the soil with other indicative properties such as CEC and erosion, as has been shown by various authors (Imeson y Vis, 1984; De Ploey & Poesen, 1985; Le Bissonnais, 1996; Boix-Fayos et al., 2001; Cammeraat y Imeson, 1998; Cerdá, 1998). As has been stated, there is a direct relationship between rainfall, organic matter content, cation exchange capacity, structural stability, and the resistence to soil erosion factor

  16. Unraveling the chemical space of terrestrial and meteoritic organic matter

    NASA Astrophysics Data System (ADS)

    Schmitt-Kopplin, Philippe; Harir, Mourad; Hertkorn, Norbert; Kanawati, Basem; Ruf, Alexander; Quirico, Eric; Bonal, Lydie; Beck, Pierre; Gabelica, Zelimir

    2015-04-01

    In terrestrial environments natural organic matter (NOM) occurs in soils, freshwater and marine environments, in the atmosphere and represents an exceedingly complex mixture of organic compounds that collectively exhibits a nearly continuous range of properties (size-reactivity continuum). In these materials, the "classical" biogeosignatures of the (biogenic and geogenic) precursor molecules, like lipids, lignins, proteins and natural products have been attenuated, often beyond recognition, during a succession of biotic and abiotic (e.g. photo- and redox chemistry) reactions. Because of this loss of biochemical signature, these materials can be designated non-repetitive complex systems. The access to extra-terrestrial organic matter is given i.e. in the analysis of meteoritic materials. Numerous descriptions of organic molecules present in organic chondrites have improved our understanding of the early interstellar chemistry that operated at or just before the birth of our solar system. However, many molecular analyses are so far targeted toward selected classes of compounds with a particular emphasis on biologically active components in the context of prebiotic chemistry. Here we demonstrate that a non-targeted ultrahigh-resolution molecular analysis of the solvent-accessible organic fraction of meteorite extracted under mild conditions allows one to extend its indigenous chemical diversity to tens of thousands of different molecular compositions and likely millions of diverse structures. The description of the molecular complexity provides hints on heteroatoms chronological assembly, shock and thermal events and revealed recently new classes of thousands of novel organic, organometallic compounds uniquely found in extra-terrestrial materials and never described in terrestrial systems. This high polymolecularity suggests that the extraterrestrial chemodiversity is high compared to terrestrial relevant biological and biogeochemical-driven chemical space. (ultra

  17. Lead sequestration and species redistribution during soil organic matter decomposition.

    PubMed

    Schroth, Andrew W; Bostick, Benjamin C; Kaste, James M; Friedland, Andrew J

    2008-05-15

    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-rayfluorescence and X-ray absorption spectroscopy. When Pb was introduced to fresh forest O(i) 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 (approximately 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.

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

    PubMed

    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. PMID:27624745

  19. Lead sequestration and species redistribution during soil organic matter decomposition

    USGS Publications Warehouse

    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.

  20. Lead Sequestration And Species Redistribution During Soil Organic Matter Decomposition

    SciTech Connect

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

    2009-05-27

    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-rayfluorescence and X-ray absorption spectroscopy. When Pb was introduced to fresh forest O{sub i} 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 ({approx}20--35%) and SOM ({approx}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.

  1. Lead Sequestration and Species Redistribution During Soil Organic Matter Decomposition

    SciTech Connect

    Schroth,A.; Bostick, B.; Kaste, J.; Friedland, A.

    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 ({approx}20-35%) and SOM ({approx}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.

  2. Missing links in the root-soil organic matter continuum

    SciTech Connect

    O'Brien, Sarah L.; Iversen, Colleen M

    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 wide

  3. Priming of soil organic matter decomposition in cryoturbated Arctic soils

    NASA Astrophysics Data System (ADS)

    Richter, A.; Wild, B.; Schnecker, J.; Rusalimova, O.

    2012-12-01

    The Arctic is subjected to particularly high rates of warming, with profound consequences for the carbon cycle: on the one hand plant productivity and C storage in plant biomass have been shown to increase strongly in many parts of the Arctic, on the other hand, increasing rates of soil organic matter (SOM) decomposition have been reported. One of the possibilities that could reconcile these observations is, that increased plant growth may lead to increased root exudation rates, which are known to stimulate microbial turnover of organic matter under certain circumstances, in a process termed "priming" of SOM. Two mechanisms have been brought forward that may be responsible for priming: first, easily assimilable material exuded by plant roots may help microbes to overcome their energy limitation and second, this input of labile carbon could lead to a nitrogen limitation of the microbial community and lead to nitrogen mining, i.e. decomposition of N-rich SOM. We here report on an incubation study with arctic soil investigating potential priming of SOM decomposition in organic topsoil horizons, cryoturbated organic matter and subsoil mineral horizons of tundra soil from the Taymyr peninsula in Siberia. We used arctic soils, that are characterized by cryoturbation (mixing of soil layers due to freezing and thawing), for this study. Turbated cryosols store more than 580 Gt C globally, a significant proportion of which is stored in the cryoturbated organic matter. We hypothesized that an increased availability of labile compounds would increase SOM decomposition rates, and that this effect would be strongest in horizons with a low natural availability of labile C, i.e. in the mineral subsoil. We amended soils with 13C labelled glucose, cellulose, amino acids or proteins, and measured the mineralization of SOM C as well as microbial community composition and potential activities of extracellular enzymes. Our results demonstrate that topsoil organic, cryoturbated and

  4. Aquatic Organic Matter Fluorescence - from phenomenon to application

    NASA Astrophysics Data System (ADS)

    Reynolds, Darren

    2014-05-01

    The use of fluorescence to quantify and characterise aquatic organic matter in river, ocean, ground water and drinking and waste waters has come along way since its discovery as a phenomenon in the early 20th century. For example, there are over 100 papers published each year in international peer reviewed journals, an order of magnitude increase since a decade ago (see Figure taken from ISI database from 1989 to 2007 for publications in the fields of river water and waste water). Since then it has been extensively used as a research tool since the 1990's by scientists and is currently used for a wide variety of applications within a number of sectors. Universities, organisations and companies that research into aquatic organic matter have either recently readily use appropriate fluorescence based techniques and instrumentation. In industry and government, the technology is being taken up by environmental regulators and water and wastewater companies. This keynote presentation will give an overview of aquatic organic matter fluorescence from its conception as a phenomenon through to its current use in a variety of emerging applications within the sectors concerned with understanding, managing and monitoring the aquatic environment. About the Speaker Darren Reynolds pioneered the use of fluorescence spectroscopy for the analysis of wastewaters in the 1990's. He currently leads a research group within the Centre for Research in Biosciences and sits on the Scientific Advisory Board for the Institute of Bio-Sensing Technology at the University of the West of England, Bristol. He is a multidisciplinary scientist concerned with the development of technology platforms for applications in the fields of environment/agri-food and health. His current research interests include the development of optical technologies and techniques for environmental and biological sensing and bio-prospecting applications. He is currently involved in the development and use of synthetic biology

  5. Persistence of soil organic matter as an ecosystem property

    SciTech Connect

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

    2011-08-15

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

  6. Particulate organic matter sinks and sources in high Arctic fjord

    NASA Astrophysics Data System (ADS)

    Kuliński, Karol; Kędra, Monika; Legeżyńska, Joanna; Gluchowska, Marta; Zaborska, Agata

    2014-11-01

    The main aim of this paper is to present results on concentrations, fluxes and isotopic composition (δ13Corg) of particulate and sedimentary organic carbon (measures of particulate and sedimentary organic matter, respectively) in Kongsfjorden, Spitsbergen. The terrestrial particulate organic carbon (POC) input to the Kongsfjorden reached 760 · 106 ± 145 · 106 g Corg y- 1, forced mostly by the glaciers' activity. This constituted 5-10% of the bulk POC supplied to the system. Marine primary production was the main source of the remaining 90-95% of POC. Organic carbon burial rates amounted to 9 ± 1 g Corg m- 2 y- 1 in the central and 13 ± 1 g Corg m- 2 y- 1 in the outer part of the fjord. Two terrestrial POM δ13Corg end members were identified: the ancient organic matter (OM) supplied by glaciers and rivers fed by water discharged from the glaciers (from - 25.4‰ to - 25.1‰), and the fresh terrestrial POM (from - 26.7‰ to - 26.6‰). Marine OM was characterized by a wide range of δ13Corg signatures: from ≤ - 26.1‰ for the phytoplankton depleted in 13Corg to ca. - 15.8‰ for debris of marine phytobenthos. The lack of distinct marine δ13Corg end member and the resemblance of phytoplankton δ13Corg signatures to the terrestrial POM δ13Corg end member precluded the use of the two δ13Corg end member mixing model to trace the terrestrial OM in Kongsfjorden, which is also very likely to happen in other Arctic regions.

  7. Association of organic matter and ferrihydrite: adsorption versus coprecipitation

    NASA Astrophysics Data System (ADS)

    Eusterhues, K.; Rennert, T.; Knicker, H.; Totsche, K. U.

    2009-04-01

    Ferrihydrite (Fh) - even if present at low concentrations - may control the available surface area and therefore, the behaviour of nutrients and pollutants in soils. Its precipitation often takes place in the presence of dissolved organic matter (OM). This involves processes such as adsorption, but also coprecipitation, flocculation/coagulation and poisoning of crystal growth. In this study, we compare coprecipitation of organic matter and ferrihydrite with pure adsorption of OM on ferrihydrite. We therefore prepared an adsorption series and a coprecipitation series using (i) water extractable organic matter from a forest topsoil and (ii) sulfite extractable lignin from paper. Products were investigated by N2-adsorption, XRD and FTIR. In coprecipitation experiments with both types of OM we observed a strong interference of the organic molecules with crystal growth leading to smaller Fh crystals, increased lattice spacings and a lower crystallinity. The highest achieved C loadings were found at approximately 200 mg C per g Fh for the adsorption and coprecipitation of the soil extract as well as for the adsorption of lignin. Coprecipitation of lignin, in contrast, resulted in a much higher maximum loading of 360 mg C per g Fh. The FTIR spectrum of the unreacted soil extract is mainly characterized by carboxyl C and polysaccharide C, with a smaller contribution of phenolic C. Spectra of the adsorbed or coprecipitated soil extract reveal weaker bands and lowered wave numbers indicating removal from solution followed by the formation of chemical bonds between the organic species and Fh by inner-sphere surface complexes. The FTIR spectrum of the lignin material shows a strong contribution of carboxyl C, polysaccharide C, and several aromatic C species. Again, all of these C species seem to form surface complexes after reaction with Fh in adsorption and coprecipitation experiments. Interestingly, at low initial C concentrations in all experiments the sorption of carboxyl

  8. Conservative or reactive? Mechanistic chemical perspectives on organic matter stability

    NASA Astrophysics Data System (ADS)

    Koch, Boris

    2016-04-01

    Carbon fixation by terrestrial and marine primary production has a fundamental seasonal effect on the atmospheric carbon content and it profoundly contributes to long-term carbon storage in form of organic matter (OM) in soils, water, and sediments. The efficacy of this sequestration process strongly depends on the degree of OM persistence. Therefore, one of the key issues in dissolved and particulate OM research is to assess the stability of reservoirs and to quantify their contribution to global carbon fluxes. Incubation experiments are helpful to assess OM stability during the first, early diagenetic turnover induced by sunlight or microbes. However, net carbon fluxes within the global carbon cycle also act on much longer time scales, which are not amenable in experiments. It is therefore critical to improve our mechanistic understanding to be able to assess potential future changes in the organic matter cycle. This session contribution highlights some achievements and open questions in the field. An improved mechanistic understanding of OM turnover particularly depends on the molecular characterization of biogeochemical processes and their kinetics: (i) in soils and sediments, aggregation/disaggregation of OM is primarily controlled by its molecular composition. Hence, the chemical composition determines the transfer of organic carbon from the large particulate to the small dissolved organic matter reservoir - an important substrate for microbial metabolism. (ii) In estuaries, dissolved organic carbon gradients usually suggest conservative behavior, whereas molecular-level studies reveal a substantial chemical modification of terrestrial DOM along the land-ocean interface. (iii) In the ocean, previous studies have shown that the recalcitrance of OM depends on bulk concentration and energy yield. However, ultrahigh resolution mass spectrometry in combination with radiocarbon analyses also emphasized that stability is tightly connected to molecular composition

  9. Advanced treatment of refractory organic pollutants in petrochemical industrial wastewater by bioactive enhanced ponds and wetland system.

    PubMed

    Liu, Shuo; Ma, Qiusha; Wang, Baozhen; Wang, Jifu; Zhang, Ying

    2014-05-01

    A large-scale combined ponds-wetland system was applied for advanced treatment of refractory pollutants in petrochemical industrial wastewater. The system was designed to enhance bioactivity and biological diversity, which consisted of anaerobic ponds (APs), facultative ponds (FPs), aerobic pond and wetland. The refractory pollutants in the petrochemical wastewater to be treated were identified as alkanes, chloroalkanes, aromatic hydrocarbons, and olefins, which were significantly degraded and transformed along with the influent flowing through the enhanced bioactive ponds-wetland system. 8 years of recent operational data revealed that the average removal rate of stable chemical oxygen demand (COD) was 42.7 % and that influent COD varied from 92.3 to 195.6 mg/L. Final effluent COD could reach 65.8 mg/L (average). COD removal rates were high in the APs and FPs and accounted for 75 % of the total amount removed. This result indicated that the APs and FPs degraded refractory pollutants through the facilitation of bacteria growth. The changes in the community structures of major microbes were assessed by 16SrDNA-denaturing gradient gel electrophoresis. The same analysis was used to identify the main bacterial function for the removal of refractory pollutants in the APs and FPs. The APs and FPs displayed similar microbial diversities, and some of the identified bacteria degraded and removed refractory pollutants. The overall results proved the applicability, stability, and high efficiency of the ponds-wetland system with enhanced bioactivity in the advanced removal of refractory pollutants from petrochemical industrial wastewater.

  10. Do organic matter matter? Contribution of organic matter on scavenging and fractionation of natural radionuclides in the Oceanic Flux Program (OFP) site of Bermuda

    NASA Astrophysics Data System (ADS)

    Chuang, C.; Santschi, P. H.; Conte, M. H.; Schumann, D.; Ayranov, M.

    2012-12-01

    Natural particle-reactive radionuclides, 234Th, 233Pa, 210Po, 210Pb and 7Be, have been used for estimating particulate organic carbon (POC) export flux in the ocean for decades. However, by simply relying on empirically determined isotope ratios to POC and other parameters, sometimes results from field studies are puzzling and become controversial (e.g., one is summarized in Li, 2005). The picture becomes clearer when it was noticed that a missing fraction, e.g., natural organic matter, could be the cause. For example, a series of field and lab studies demonstrated that biopolymers excreted by marine micro-organisms are likely carrier molecules for a number of these isotopes (e.g., Guo et al., 2002; Quigley et al., 2002; Santschi et al., 2003; Roberts et al., 2009; Hung et al., 2010; Xu et al., 2011; Hung et al., 2012; Yang et al., 2012). To examine the effect of organic composition of the particle on the scavenging and fractionation of selected natural radionuclides (e.g., Th, Pa, Pb, Po, Be), organic composition (e.g., protein, polysaccharides, uronic acid, siderophore and amino acid contents, and etc.) and particle-water partition coefficients (Kd) were determined for sediment trap material collected in the Oceanic Flux Program (OFP) site of Bermuda (500, 1500 and 3200 m). Results showed that different organic components contribute differently to the fractionation of different radionuclides from the three depths. We conclude that natural organic matter control on the particle-water partition coefficients cannot be ignored.

  11. Simplified method to assess soil organic matter in landscape and carbon sequestration studies

    NASA Astrophysics Data System (ADS)

    Pallasser, Robert; Minasny, Budiman; McBratney, Alex; de Bruyn, Hank

    2010-05-01

    Soil organic matter (SOM) is composed of a variety of carbon bearing forms which are variably susceptible to degradation, itself a function of soil conditions (moisture, permeability, pH, Eh). Stability and residence time have become key questions relevant to soil carbon storage. Interestingly, organic matter types also differ in terms of their refractory stabilities making thermal analysis potentially an ideal way to resolve and analyse SOM. Elemental analyses of soils are routinely used to provide accurate total carbon determinations for the subsamples in question but cannot yield information about the relative amounts of labile to more stable carbon without involved chemical pre-treatment. Thermogravimetric analyses (TGA) have been commonly used to characterise chemical decomposition and to provide distinctive fingerprints (due to discrete mass changes) for mineral and organic materials. Such discrete changes in mass appear as peaks when registered on a DTGA (differential TGA) plot and correspond with dehydration, denaturing or oxidation events. Soil being a more complex continuum of organic and inorganic substances, many from fermentation reactions and microbial waste, does not have one particular fingerprint. Nonetheless, a number of relevant organic substances have characteristically different but consistent ignition temperatures (Lopez-Capel et. al., 2006; Laird et al., 2008; Xie et. al., 2009) allowing carbon pools to be distinguished thermally. In our studies, oxidative DTGA analyses of soils using a TA 2590 were typified by a bimodal distribution in SOM representing one less stable and one more stable group, a pattern similarly described by Siewert (2004). Current experiments indicate that the relative proportions of these SOM pulses are fairly reproducible but vary depending on soils and sampling depth (i.e. conditions) enabling it as a diagnostic parameter when considering SOM dynamics and humification. In order to compare this property numerically

  12. How does pyrogenic organic matter affect the N dynamic in agricultural soils? An incubation study

    NASA Astrophysics Data System (ADS)

    de La Rosa, José M.; Knicker, Heike

    2010-05-01

    Besides other environmental factors, N availability drives the carbon (C) and nitrogen (N) cycles in grasslands. Since grass-dominated ecosystems cover approximately 40% of the terrestrial surface and store more than 30% of global soil organic carbon (SOC), alterations to those ecosystems could have significant consequences and potential implications for global C and N cycles and climate (Schlesinger et al., 1990). Understanding the processes that govern the efficient cycling of nutrients through soil/plant systems remains an important topic to underpin the choice of strategies aimed at ensuring the long-term sustainability of ecosystems. In Mediterranean ecosystems, wild-fires occur frequently. Whereas factors such as water shortage or erosion contribute to reduced N-availability by lowering the litter input, burning additionally increase the refractory N and C-pools by charring litter and humic material (charred pyrogenic organic matter-PyOM) (Gonzalez-Pérez, 2004). In general, the addition of organic matter either as plant residues or farmyard manure has been shown to significantly increase biological activity, microbial biomass and enzyme activity in soil (Dick, 1992). Even in situations where microbial biomass appears to be unaffected, the activity of specific processes (e.g. N mineralization) can be significantly influenced by the addition of organic residues). However, little is known about the changes of the N cycle caused by the addition of PyOM. Therefore, the interest of our research was to study the impact of 15N enriched-biochars either alone or in conjunction with a 15N enriched fertilizer (K15NO3) on aggregate stability and organic carbon (C) and nitrogen (N) distribution among the different soil fractions. The latter may help to elucidate both, the quality of the stored organic matter and if the accumulation is related to interaction with the mineral matter. Therefore, biochar derived from grass material grown on 15N-enriched fertilizer was added

  13. Molecular insights into the microbial formation of marine dissolved organic matter: recalcitrant or labile?

    NASA Astrophysics Data System (ADS)

    Koch, B. P.; Kattner, G.; Witt, M.; Passow, U.

    2014-08-01

    The degradation of marine dissolved organic matter (DOM) is an important control variable in the global carbon cycle. For our understanding of the kinetics of organic matter cycling in the ocean, it is crucial to achieve a mechanistic and molecular understanding of its transformation processes. A long-term microbial experiment was performed to follow the production of non-labile DOM by marine bacteria. Two different glucose concentrations and dissolved algal exudates were used as substrates. We monitored the bacterial abundance, concentrations of dissolved and particulate organic carbon (DOC, POC), nutrients, amino acids and transparent exopolymer particles (TEP) for 2 years. The molecular characterization of extracted DOM was performed by ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) after 70 days and after ∼2 years of incubation. Although glucose quickly degraded, a non-labile DOC background (5-9% of the initial DOC) was generated in the glucose incubations. Only 20% of the organic carbon from the algal exudate degraded within the 2 years of incubation. The degradation rates for the non-labile DOC background in the different treatments varied between 1 and 11 μmol DOC L-1 year-1. Transparent exopolymer particles, which are released by microorganisms, were produced during glucose degradation but decreased back to half of the maximum concentration within less than 3 weeks (degradation rate: 25 μg xanthan gum equivalents L-1 d-1) and were below detection in all treatments after 2 years. Additional glucose was added after 2 years to test whether labile substrate can promote the degradation of background DOC (co-metabolism; priming effect). A priming effect was not observed but the glucose addition led to a slight increase of background DOC. The molecular analysis demonstrated that DOM generated during glucose degradation differed appreciably from DOM transformed during the degradation of the algal exudates. Our

  14. Influence of dissolved organic carbon content on modelling natural organic matter acid-base properties.

    PubMed

    Garnier, Cédric; Mounier, Stéphane; Benaïm, Jean Yves

    2004-10-01

    Natural organic matter (NOM) behaviour towards proton is an important parameter to understand NOM fate in the environment. Moreover, it is necessary to determine NOM acid-base properties before investigating trace metals complexation by natural organic matter. This work focuses on the possibility to determine these acid-base properties by accurate and simple titrations, even at low organic matter concentrations. So, the experiments were conducted on concentrated and diluted solutions of extracted humic and fulvic acid from Laurentian River, on concentrated and diluted model solutions of well-known simple molecules (acetic and phenolic acids), and on natural samples from the Seine river (France) which are not pre-concentrated. Titration experiments were modelled by a 6 acidic-sites discrete model, except for the model solutions. The modelling software used, called PROSECE (Programme d'Optimisation et de SpEciation Chimique dans l'Environnement), has been developed in our laboratory, is based on the mass balance equilibrium resolution. The results obtained on extracted organic matter and model solutions point out a threshold value for a confident determination of the studied organic matter acid-base properties. They also show an aberrant decreasing carboxylic/phenolic ratio with increasing sample dilution. This shift is neither due to any conformational effect, since it is also observed on model solutions, nor to ionic strength variations which is controlled during all experiments. On the other hand, it could be the result of an electrode troubleshooting occurring at basic pH values, which effect is amplified at low total concentration of acidic sites. So, in our conditions, the limit for a correct modelling of NOM acid-base properties is defined as 0.04 meq of total analysed acidic sites concentration. As for the analysed natural samples, due to their high acidic sites content, it is possible to model their behaviour despite the low organic carbon concentration.

  15. The abiotic degradation of soil organic matter to oxalic acid

    NASA Astrophysics Data System (ADS)

    Studenroth, Sabine; Huber, Stefan; Schöler, H. F.

    2010-05-01

    The abiotic degradation of soil organic matter to volatile organic compounds was studied intensely over the last years (Keppler et al., 2000; Huber et al., 2009). It was shown that soil organic matter is oxidised due to the presence of iron (III), hydrogen peroxide and chloride and thereby produces diverse alkyl halides, which are emitted into the atmosphere. The formation of polar halogenated compounds like chlorinated acetic acids which are relevant toxic environmental substances was also found in soils and sediments (Kilian et al., 2002). The investigation of the formation of other polar halogenated and non-halogenated compounds like diverse mono- and dicarboxylic acids is going to attain more and more importance. Due to its high acidity oxalic acid might have impacts on the environment e.g., nutrient leaching, plant diseases and negative influence on microbial growth. In this study, the abiotic formation of oxalic acid in soil is examined. For a better understanding of natural degradation processes mechanistic studies were conducted using the model compound catechol as representative for structural elements of the humic substances and its reaction with iron (III) and hydrogen peroxide. Iron is one of the most abundant elements on earth and hydrogen peroxide is produced by bacteria or through incomplete reduction of oxygen. To find suitable parameters for an optimal reaction and a qualitative and quantitative analysis method the following reaction parameters are varied: concentration of iron (III) and hydrogen peroxide, time dependence, pH-value and influence of chloride. Analysis of oxalic acid was performed employing an ion chromatograph equipped with a conductivity detector. The time dependent reaction shows a relatively fast formation of oxalic acid, the optimum yield is achieved after 60 minutes. Compared to the concentration of catechol an excess of hydrogen peroxide as well as a low concentration of iron (III) are required. In absence of chloride the

  16. Morphological Study of Insoluble Organic Matter Residues from Primitive

    NASA Technical Reports Server (NTRS)

    Changela, H. G.; Stroud, R. M.; Peeters, Z.; Nittler, L. R.; Alexander, C. M. O'D.; DeGregorio, B. T.; Cody, G. D.

    2012-01-01

    Insoluble organic matter (IOM) constitutes a major proportion, 70-99%, of the total organic carbon found in primitive chondrites [1, 2]. One characteristic morphological component of IOM is nanoglobules [3, 4]. Some nanoglobules exhibit large N-15 and D enrichments relative to solar values, indicating that they likely originated in the ISM or the outskirts of the protoplanetary disk [3]. A recent study of samples from the Tagish Lake meteorite with varying levels of hydrothermal alteration suggest that nanoglobule abundance decreases with increasing hydrothermal alteration [5]. The aim of this study is to further document the morphologies of IOM from a range of primitive chondrites in order to determine any correlation of morphology with petrographic grade and chondrite class that could constrain the formation and/or alteration mechanisms.

  17. Nature and transformation of dissolved organic matter in treatment wetlands

    USGS Publications Warehouse

    Barber, L.B.; Leenheer, J.A.; Noyes, T.I.; Stiles, E.A.

    2001-01-01

    This investigation into the occurrence, character, and transformation of dissolved organic matter (DOM) in treatment wetlands in the western United States shows that (i) the nature of DOM in the source water has a major influence on transformations that occur during treatment, (ii) the climate factors have a secondary effect on transformations, (iii) the wetlands receiving treated wastewater can produce a net increase in DOM, and (iv) the hierarchical analytical approach used in this study can measure the subtle DOM transformations that occur. As wastewater treatment plant effluent passes through treatment wetlands, the DOM undergoes transformation to become more aromatic and oxygenated. Autochthonous sources are contributed to the DOM, the nature of which is governed by the developmental stage of the wetland system as well as vegetation patterns. Concentrations of specific wastewaterderived organic contaminants such as linear alkylbenzene sulfonate, caffeine, and ethylenediaminetetraacetic acid were significantly attenuated by wetland treatment and were not contributed by internal loading.

  18. Literature review of organic matter transport from marshes

    NASA Technical Reports Server (NTRS)

    Dow, D. D.

    1982-01-01

    A conceptual model for estimating a transport coefficient for the movement of nonliving organic matter from wetlands to the adjacent embayments was developed in a manner that makes it compatible with the Earth Resources Laboratory's Productive Capacity Model. The model, which envisages detritus movement from wetland pixels to the nearest land-water boundary followed by movement within the water column from tidal creeks to the adjacent embayment, can be transposed to deal with only the interaction between tidal water and the marsh or to estimate the transport from embayments to the adjacent coastal waters. The outwelling hypothesis postulated wetlands as supporting coastal fisheries either by exporting nutrients, such as inorganic nitrogen, which stimulated the plankton-based grazing food chain in the water column, or through the export of dissolved and particulate organic carbon which provided a benthic, detritus-based food web which provides the food source for the grazing food chain in a more indirect fashion.

  19. Carbon isotope fractionation of sapropelic organic matter during early diagenesis

    USGS Publications Warehouse

    Spiker, E. C.; Hatcher, P.G.

    1984-01-01

    Study of an algal, sapropelic sediment from Mangrove Lake, Bermuda shows that the mass balance of carbon and stable carbon isotopes in the major organic constituents is accounted for by a relatively straightforward model of selective preservation during diagenesis. The loss of 13C-enriched carbohydrates is the principal factor controlling the intermolecular mass balance of 13C in the sapropel. Results indicate that labile components are decomposed leaving as a residual concentrate in the sediment an insoluble humic substance that may be an original biochemical component of algae and associated bacteria. An overall decrease of up to about 4??? in the ?? 13C values of the organic matter is observed as a result of early diagenesis. ?? 1984.

  20. Ironing out the details of soil organic matter cycling: The unique role of Fe-bearing minerals in regulating organic matter transformation in soils

    NASA Astrophysics Data System (ADS)

    Heckman, K. A.; Lawrence, C. R.; Harden, J. W.; Crate, J.; Swanston, C.

    2015-12-01

    Interest in the influence of mineral chemistry on soil organic matter cycling has been steadily growing, with the role of iron specifically garnering a great deal of attention. Empirical evidence from both lab and field based studies suggest that the interactions of Fe-bearing minerals and colloidal Fe species are unique from the interactions of the soil mineral matrix as a whole and may have a disproportionate influence on soil organic matter. We present results from a suite of studies examining Fe-organic matter interactions which utilize a broad range of technical approaches and highlight the use of radiocarbon analysis in terrestrial carbon cycle studies. Data suggests that interaction of organics with Fe-bearing moieties induces consistent partitioning of organics between dissolved and surface bound organic matter pools, including significant consequences for N and P availability and biodegradability of soil organic matter. Selective dissolution techniques have revealed that Fe-humus complexes comprise a significant pool of soil organic matter which cycles on a shorter-term basis across a variety of ecosystems types, while sequential density separation combined with x-ray diffraction imply concentration and long-term preservation of N-rich organics on Fe-bearing crystalline mineral surfaces. Our results explore the unique and multifaceted roles of Fe in regulating organic matter transformation and preservation in a range of soil types.

  1. Dissolved organic matter photolysis in Canadian arctic thaw ponds

    NASA Astrophysics Data System (ADS)

    Laurion, Isabelle; Mladenov, Natalie

    2013-09-01

    The abundant thaw lakes and ponds in the circumarctic receive a new pool of organic carbon as permafrost peat soils degrade, which can be exposed to significant irradiance that potentially increases as climate warms and ice cover shortens. Exposure to sunlight is known to accelerate the transformation of dissolved organic matter (DOM) into molecules that can be more readily used by microbes. We sampled the water from two common classes of ponds found in the ice-wedge system of continuous permafrost regions of Canada, polygonal and runnel ponds, and followed the transformation of DOM over 12 days by looking at dissolved organic carbon (DOC) concentration and DOM absorption and fluorescence properties. The results indicate a relatively fast decay of color (3.4 and 1.6% loss d-1 of absorption at 320 nm for the polygonal and runnel pond, respectively) and fluorescence (6.1 and 8.3% loss d-1 of total fluorescent components, respectively) at the pond surface, faster in the case of humic-like components, but insignificant losses of DOC over the observed period. This result indicates that direct DOM mineralization (photochemical production of CO2) is apparently minor in thaw ponds compared to the photochemical transformation of DOM into less chromophoric and likely more labile molecules with a greater potential for microbial mineralization. Therefore, DOM photolysis in arctic thaw ponds can be considered as a catalytic mechanism, accelerating the microbial turnover of mobilized organic matter from thawing permafrost and the production of greenhouse gases, especially in the most shallow ponds. Under a warming climate, this mechanism will intensify as summers lengthen.

  2. Terrestrial and marine perspectives on modeling organic matter degradation pathways.

    PubMed

    Burd, Adrian B; Frey, Serita; Cabre, Anna; Ito, Takamitsu; Levine, Naomi M; Lønborg, Christian; Long, Matthew; Mauritz, Marguerite; Thomas, R Quinn; Stephens, Brandon M; Vanwalleghem, Tom; Zeng, Ning

    2016-01-01

    Organic matter (OM) plays a major role in both terrestrial and oceanic biogeochemical cycles. The amount of carbon stored in these systems is far greater than that of carbon dioxide (CO2 ) in the atmosphere, and annual fluxes of CO2 from these pools to the atmosphere exceed those from fossil fuel combustion. Understanding the processes that determine the fate of detrital material is important for predicting the effects that climate change will have on feedbacks to the global carbon cycle. However, Earth System Models (ESMs) typically utilize very simple formulations of processes affecting the mineralization and storage of detrital OM. Recent changes in our view of the nature of this material and the factors controlling its transformation have yet to find their way into models. In this review, we highlight the current understanding of the role and cycling of detrital OM in terrestrial and marine systems and examine how this pool of material is represented in ESMs. We include a discussion of the different mineralization pathways available as organic matter moves from soils, through inland waters to coastal systems and ultimately into open ocean environments. We argue that there is strong commonality between aspects of OM transformation in both terrestrial and marine systems and that our respective scientific communities would benefit from closer collaboration. PMID:26015089

  3. Photochemical and Nonphotochemical Transformations of Cysteine with Dissolved Organic Matter.

    PubMed

    Chu, Chiheng; Erickson, Paul R; Lundeen, Rachel A; Stamatelatos, Dimitrios; Alaimo, Peter J; Latch, Douglas E; McNeill, Kristopher

    2016-06-21

    Cysteine (Cys) plays numerous key roles in the biogeochemistry of natural waters. Despite its importance, a full assessment of Cys abiotic transformation kinetics, products and pathways under environmental conditions has not been conducted. This study is a mechanistic evaluation of the photochemical and nonphotochemical (dark) transformations of Cys in solutions containing chromophoric dissolved organic matter (CDOM). The results show that Cys underwent abiotic transformations under both dark and irradiated conditions. Under dark conditions, the transformation rates of Cys were moderate and were highly pH- and temperature-dependent. Under UVA or natural sunlight irradiations, Cys transformation rates were enhanced by up to two orders of magnitude compared to rates under dark conditions. Product analysis indicated cystine and cysteine sulfinic acid were the major photooxidation products. In addition, this study provides an assessment of the contributions of singlet oxygen, hydroxyl radical, hydrogen peroxide, and triplet dissolved organic matter to the CDOM-sensitized photochemical oxidation of Cys. The results suggest that another unknown pathway was dominant in the CDOM-sensitized photodegradation of Cys, which will require further study to identify. PMID:27172378

  4. Terrestrial and marine perspectives on modeling organic matter degradation pathways.

    PubMed

    Burd, Adrian B; Frey, Serita; Cabre, Anna; Ito, Takamitsu; Levine, Naomi M; Lønborg, Christian; Long, Matthew; Mauritz, Marguerite; Thomas, R Quinn; Stephens, Brandon M; Vanwalleghem, Tom; Zeng, Ning

    2016-01-01

    Organic matter (OM) plays a major role in both terrestrial and oceanic biogeochemical cycles. The amount of carbon stored in these systems is far greater than that of carbon dioxide (CO2 ) in the atmosphere, and annual fluxes of CO2 from these pools to the atmosphere exceed those from fossil fuel combustion. Understanding the processes that determine the fate of detrital material is important for predicting the effects that climate change will have on feedbacks to the global carbon cycle. However, Earth System Models (ESMs) typically utilize very simple formulations of processes affecting the mineralization and storage of detrital OM. Recent changes in our view of the nature of this material and the factors controlling its transformation have yet to find their way into models. In this review, we highlight the current understanding of the role and cycling of detrital OM in terrestrial and marine systems and examine how this pool of material is represented in ESMs. We include a discussion of the different mineralization pathways available as organic matter moves from soils, through inland waters to coastal systems and ultimately into open ocean environments. We argue that there is strong commonality between aspects of OM transformation in both terrestrial and marine systems and that our respective scientific communities would benefit from closer collaboration.

  5. Photosensitizing properties of water-extractable organic matter from soils.

    PubMed

    Nkhili, Ezzhora; Boguta, Patrycja; Bejger, Romualda; Guyot, Ghislain; Sokołowska, Zofia; Richard, Claire

    2014-01-01

    Water-extractable organic matter (WEOM) was extracted using pure water from two black soils and from the Elliott reference soil of the International Humic Substances Society (IHSS). WEOMs were characterized by chemical and spectroscopic methods. The apparent quantum yields of singlet oxygen, triplet excited states and hydroxyl radicals formation upon irradiation within the wavelength range 290-450 nm were determined using chemical probes and compared to those of standard Elliott humic substances. In general, the aromatic content, as measured by the SUVA value, was close in WEOMs and humic substances, while the E2/E3 was higher and the humification index lower in the former. Quantum yield values measured for WEOMs fell within the range of those found for basic medium extracted humic substances or were even higher in one case. Thus, water soluble aromatic moiety of the soil organic matter, especially those with low humification degree, is important for the photosensitizing properties. We also found that WEOMs sensitized the bisphenol A phototransformation with rates of the same order of magnitude for all the samples.

  6. Black Carbon - Soil Organic Matter abiotic and biotic interactions

    NASA Astrophysics Data System (ADS)

    Cotrufo, Francesca; Boot, Claudia; Denef, Karolien; Foster, Erika; Haddix, Michelle; Jiang, Xinyu; Soong, Jennifer; Stewart, Catherine

    2014-05-01

    Wildfires, prescribed burns and the use of char as a soil amendment all add large quantities of black carbon to soils, with profound, yet poorly understood, effects on soil biology and chemical-physical structure. We will present results emerging from our black carbon program, which addresses questions concerning: 1) black carbon-soil organic matter interactions, 2) char decomposition and 3) impacts on microbial community structure and activities. Our understanding derives from a complementary set of post-fire black carbon field surveys and laboratory and field experiments with grass and wood char amendments, in which we used molecular (i.e., BPCA, PLFA) and isotopic (i.e., 13C and 15N labelled char) tracers. Overall, emerging results demonstrate that char additions to soil are prone to fast erosion, but a fraction remains that increases water retention and creates a better environment for the microbial community, particularly favoring gram negative bacteria. However, microbial decomposition of black carbon only slowly consumes a small fraction of it, thus char still significantly contributes to soil carbon sequestration. This is especially true in soils with little organic matter, where black carbon additions may even induce negative priming.

  7. Wastewater disinfection and organic matter removal using ferrate (VI) oxidation.

    PubMed

    Bandala, Erick R; Miranda, Jocelyn; Beltran, Margarita; Vaca, Mabel; López, Raymundo; Torres, Luis G

    2009-09-01

    The use of iron in a +6 valence state, (Fe (VI), as FeO4(-2)) was tested as a novel alternative for wastewater disinfection and decontamination. The removal of organic matter (OM) and index microorganisms present in an effluent of a wastewater plant was determined using FeO4(-2) without any pH adjustment. It was observed that concentrations of FeO4(-2) ranging between 5 and 14 mg l(-1) inactivated up to 4-log of the index microorganisms (initial concentration c.a. 10(6) CFU/100 ml) and achieved OM removal up to almost 50%. The performance of FeO4(-2) was compared with OM oxidation and disinfection using hypochlorite. It was observed that hypochlorite was less effective in OM oxidation and coliform inactivation than ferrate. Results of this work suggest that FeO4(-2) could be an interesting oxidant able to deactivate pathogenic microorganisms in water with high OM content and readily oxidize organic matter without jeopardizing its efficiency on microorganism inactivation.

  8. Wastewater disinfection and organic matter removal using ferrate (VI) oxidation.

    PubMed

    Bandala, Erick R; Miranda, Jocelyn; Beltran, Margarita; Vaca, Mabel; López, Raymundo; Torres, Luis G

    2009-09-01

    The use of iron in a +6 valence state, (Fe (VI), as FeO4(-2)) was tested as a novel alternative for wastewater disinfection and decontamination. The removal of organic matter (OM) and index microorganisms present in an effluent of a wastewater plant was determined using FeO4(-2) without any pH adjustment. It was observed that concentrations of FeO4(-2) ranging between 5 and 14 mg l(-1) inactivated up to 4-log of the index microorganisms (initial concentration c.a. 10(6) CFU/100 ml) and achieved OM removal up to almost 50%. The performance of FeO4(-2) was compared with OM oxidation and disinfection using hypochlorite. It was observed that hypochlorite was less effective in OM oxidation and coliform inactivation than ferrate. Results of this work suggest that FeO4(-2) could be an interesting oxidant able to deactivate pathogenic microorganisms in water with high OM content and readily oxidize organic matter without jeopardizing its efficiency on microorganism inactivation. PMID:19491501

  9. Photochemical and Nonphotochemical Transformations of Cysteine with Dissolved Organic Matter.

    PubMed

    Chu, Chiheng; Erickson, Paul R; Lundeen, Rachel A; Stamatelatos, Dimitrios; Alaimo, Peter J; Latch, Douglas E; McNeill, Kristopher

    2016-06-21

    Cysteine (Cys) plays numerous key roles in the biogeochemistry of natural waters. Despite its importance, a full assessment of Cys abiotic transformation kinetics, products and pathways under environmental conditions has not been conducted. This study is a mechanistic evaluation of the photochemical and nonphotochemical (dark) transformations of Cys in solutions containing chromophoric dissolved organic matter (CDOM). The results show that Cys underwent abiotic transformations under both dark and irradiated conditions. Under dark conditions, the transformation rates of Cys were moderate and were highly pH- and temperature-dependent. Under UVA or natural sunlight irradiations, Cys transformation rates were enhanced by up to two orders of magnitude compared to rates under dark conditions. Product analysis indicated cystine and cysteine sulfinic acid were the major photooxidation products. In addition, this study provides an assessment of the contributions of singlet oxygen, hydroxyl radical, hydrogen peroxide, and triplet dissolved organic matter to the CDOM-sensitized photochemical oxidation of Cys. The results suggest that another unknown pathway was dominant in the CDOM-sensitized photodegradation of Cys, which will require further study to identify.

  10. CO2 Losses from Terrestrial Organic Matter through Photodegradation

    NASA Astrophysics Data System (ADS)

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

    2010-12-01

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

  11. Climate Change Impacts on Soil Organic Matter: New Insights from Molecular-Level Studies

    NASA Astrophysics Data System (ADS)

    Simpson, M. J.; Feng, X.; Simpson, A.

    2009-05-01

    Natural organic matter is ubiquitously found in the environment and plays a critical role in several biogeochemical processes such as the regulation of atmospheric CO2, agricultural sustainability, and the fate and transport of problematic organic chemicals in the environment. Organic matter preserved within the sedimentary record also holds key information about early life on earth, insights into past climates, and the presence of specific organic matter structures is often used in the search for life on other planets. Despite the importance of natural organic matter in several disciplines, the vast majority of organic matter remains "molecularly uncharacterized" (Hedges et al. 2000, Org. Geochem. 31:945-958). The lack of organic matter structural information is mostly due to the complex nature and uniqueness of organic matter but also due to the lack of sophisticated analytical strategies designed specifically for the study of organic matter structure and environmental reactivity. Organic matter is a collection of compounds from various plant, microbial, and anthropogenic sources, all at various stages of oxidation (decomposition) and represents the most naturally occurring complex mixture on earth. Organic geochemists have long used biomarker methods to study the sources, structures, and stage of organic matter oxidation however biomarker methods only extract and measure a small fraction of the total organic matter composition. Nuclear magnetic resonance (NMR), namely solid-state 13C NMR spectroscopy, has been used extensively to study organic matter structure but suffers from poor spectral resolution due to organic matter heterogeneity and strong dipolar coupling in solids. This presentation will highlight the development of molecular-level analytical methods for organic matter and demonstrate their utility in studying soil organic matter biogeochemistry with global warming. The use of biomarker methods with conventional and innovative NMR methods in tandem

  12. Sulfur species behavior in soil organic matter during decomposition

    USGS Publications Warehouse

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

    2007-01-01

    Soil organic matter (SOM) is a primary re??servoir of terrestrial sulfur (S), but its role in the global S cycle remains poorly understood. We examine S speciation by X-ray absorption near-edge structure (XANES) spectroscopy to describe S species behavior during SOM decomposition. Sulfur species in SOM were best represented by organic sulfide, sulfoxide, sulfonate, and sulfate. The highest fraction of S in litter was organic sulfide, but as decomposition progressed, relative fractions of sulfonate and sulfate generally increased. Over 6-month laboratory incubations, organic sulfide was most reactive, suggesting that a fraction of this species was associated with a highly labile pool of SOM. During humification, relative concentrations of sulfoxide consistently decreased, demonstrating the importance of sulfoxide as a reactive S phase in soil. Sulfonate fractional abundance increased during humification irrespective of litter type, illustrating its relative stability in soils. The proportion of S species did not differ systematically by litter type, but organic sulfide became less abundant in conifer SOM during decomposition, while sulfate fractional abundance increased. Conversely, deciduous SOM exhibited lesser or nonexistent shifts in organic sulfide and sulfate fractions during decomposition, possibly suggesting that S reactivity in deciduous litter is coupled to rapid C mineralization and independent of S speciation. All trends were consistent in soils across study sites. We conclude that S reactivity is related to spqciation in SOM, particularly in conifer forests, and S species fractions in SOM change, during decomposition. Our data highlight the importance of intermediate valence species (sulfoxide and sulfonate) in the pedochemical cycling of organic bound S. Copyright 2007 by the American Geophysical Union.

  13. Characterisation of algal organic matter produced by bloom-forming marine and freshwater algae.

    PubMed

    Villacorte, L O; Ekowati, Y; Neu, T R; Kleijn, J M; Winters, H; Amy, G; Schippers, J C; Kennedy, M D

    2015-04-15

    Algal blooms can seriously affect the operation of water treatment processes including low pressure (micro- and ultra-filtration) and high pressure (nanofiltration and reverse osmosis) membranes mainly due to accumulation of algal-derived organic matter (AOM). In this study, the different components of AOM extracted from three common species of bloom-forming algae (Alexandrium tamarense, Chaetoceros affinis and Microcystis sp.) were characterised employing various analytical techniques, such as liquid chromatography - organic carbon detection, fluorescence spectroscopy, fourier transform infrared spectroscopy, alcian blue staining and lectin staining coupled with laser scanning microscopy to indentify its composition and force measurement using atomic force microscopy to measure its stickiness. Batch culture monitoring of the three algal species illustrated varying characteristics in terms of growth pattern, cell concentration and AOM release. The AOM produced by the three algal species comprised mainly biopolymers (e.g., polysaccharides and proteins) but some refractory compounds (e.g., humic-like substances) and other low molecular weight acid and neutral compounds were also found. Biopolymers containing fucose and sulphated functional groups were found in all AOM samples while the presence of other functional groups varied between different species. A large majority (>80%) of the acidic polysaccharide components (in terms of transparent exopolymer particles) were found in the colloidal size range (<0.4 μm). The relative stickiness of AOM substantially varied between algal species and that the cohesion between AOM-coated surfaces was much stronger than the adhesion of AOM on AOM-free surfaces. Overall, the composition as well as the physico-chemical characteristics (e.g., stickiness) of AOM will likely dictate the severity of fouling in membrane systems during algal blooms. PMID:25682049

  14. Dissolved organic matter concentration and quality influences upon structure and function of freshwater microbial communities.

    PubMed

    Docherty, Kathryn M; Young, Katherine C; Maurice, Patricia A; Bridgham, Scott D

    2006-10-01

    Past studies have suggested that the concentration and quality of dissolved organic matter (DOM) may influence microbial community structure. In this study, we cross-inoculated the bacterial communities from two streams and a dystrophic lake that varied in DOM concentration and chemistry, to yield nine fully crossed treatments. We measured dissolved organic carbon (DOC) concentration and heterotrophic microbial community productivity throughout a 72-h incubation period, characterized DOM quality by molecular weight, and determined microbial community structure at the initial and final time points. Our results indicate that all bacterial inoculate sources had similar effects upon DOC concentration and DOM quality, regardless of the DOM source. These effects included an overall decrease in DOM M (W) and an initial period of DOC concentration variability between 0-24h. In contrast, microbial communities and their metabolic rates converged to profiles that reflected the DOM source upon which they were growing, regardless of the initial bacterial inoculation. The one exception was that the bacterial community from the low-concentration and low-molecular-weight DOM source exhibited a greater denaturing gradient gel electrophoresis (DGGE) band richness when grown in its own DOM source than when grown in the highest concentration and molecular weight DOM source. This treatment also exhibited a higher rate of productivity. In general, our data suggest that microbial communities are selected by the DOM sources to which they are exposed. A microbial community will utilize the low-molecular-weight (or labile) DOM sources as well as parts of the high-molecular-weight (refractory) DOM, until a community develops that can efficiently metabolize the more abundant high-molecular-weight source. This experiment examines some of the complex interactions between microbial community selection and the combined factors of DOM quality and concentration. Our data suggest that the roles of

  15. Characterisation of algal organic matter produced by bloom-forming marine and freshwater algae.

    PubMed

    Villacorte, L O; Ekowati, Y; Neu, T R; Kleijn, J M; Winters, H; Amy, G; Schippers, J C; Kennedy, M D

    2015-04-15

    Algal blooms can seriously affect the operation of water treatment processes including low pressure (micro- and ultra-filtration) and high pressure (nanofiltration and reverse osmosis) membranes mainly due to accumulation of algal-derived organic matter (AOM). In this study, the different components of AOM extracted from three common species of bloom-forming algae (Alexandrium tamarense, Chaetoceros affinis and Microcystis sp.) were characterised employing various analytical techniques, such as liquid chromatography - organic carbon detection, fluorescence spectroscopy, fourier transform infrared spectroscopy, alcian blue staining and lectin staining coupled with laser scanning microscopy to indentify its composition and force measurement using atomic force microscopy to measure its stickiness. Batch culture monitoring of the three algal species illustrated varying characteristics in terms of growth pattern, cell concentration and AOM release. The AOM produced by the three algal species comprised mainly biopolymers (e.g., polysaccharides and proteins) but some refractory compounds (e.g., humic-like substances) and other low molecular weight acid and neutral compounds were also found. Biopolymers containing fucose and sulphated functional groups were found in all AOM samples while the presence of other functional groups varied between different species. A large majority (>80%) of the acidic polysaccharide components (in terms of transparent exopolymer particles) were found in the colloidal size range (<0.4 μm). The relative stickiness of AOM substantially varied between algal species and that the cohesion between AOM-coated surfaces was much stronger than the adhesion of AOM on AOM-free surfaces. Overall, the composition as well as the physico-chemical characteristics (e.g., stickiness) of AOM will likely dictate the severity of fouling in membrane systems during algal blooms.

  16. Potential enzyme activities in cryoturbated organic matter of arctic soils

    NASA Astrophysics Data System (ADS)

    Schnecker, J.; Wild, B.; Rusalimova, O.; Mikutta, R.; Guggenberger, G.; Richter, A.

    2012-12-01

    An estimated 581 Gt organic carbon is stored in arctic soils that are affected by cryoturbtion, more than in today's atmosphere (450 Gt). The high amount of organic carbon is, amongst other factors, due to topsoil organic matter (OM) that has been subducted by freeze-thaw processes. This cryoturbated OM is usually hundreds to thousands of years old, while the chemical composition remains largely unaltered. It has therefore been suggested, that the retarded decomposition rates cannot be explained by unfavourable abiotic conditions in deeper soil layers alone. Since decomposition of soil organic material is dependent on extracellular enzymes, we measured potential and actual extracellular enzyme activities in organic topsoil, mineral subsoil and cryoturbated material from three different tundra sites, in Zackenberg (Greenland) and Cherskii (North-East Siberia). In addition we analysed the microbial community structure by PLFAs. Hydrolytic enzyme activities, calculated on a per gram dry mass basis, were higher in organic topsoil horizons than in cryoturbated horizons, which in turn were higher than in mineral horizons. When calculated on per gram carbon basis, the activity of the carbon acquiring enzyme exoglucanase was not significantly different between cryoturbated and topsoil organic horizons in any of the three sites. Oxidative enzymes, i.e. phenoloxidase and peroxidase, responsible for degradation of complex organic substances, showed higher activities in topsoil organic and cryoturbated horizons than in mineral horizons, when calculated per gram dry mass. Specific activities (per g C) however were highest in mineral horizons. We also measured actual cellulase activities (by inhibiting microbial uptake of products and without substrate addition): calculated per g C, the activities were up to ten times as high in organic topsoil compared to cryoturbated and mineral horizons, the latter not being significantly different. The total amount of PLFAs, as a proxy for

  17. DETOXIFICATION OF OUTFALL WATER USING NATURAL ORGANIC MATTER

    SciTech Connect

    Halverson, N.; Looney, B.; Millings, M.; Nichols, R.; Noonkester, J.; Payne, B.

    2010-07-13

    To protect stream organisms in an ephemeral stream at the Savannah River Site, a proposed National Pollutant Discharge Elimination System (NPDES) permit reduced the copper limit from 25 {micro}g/l to 6 {micro}g/l at Outfall H-12. Efforts to reduce copper in the wastewater and stormwater draining to this outfall did not succeed in bringing copper levels below this limit. Numerous treatment methods were considered, including traditional methods such as ion exchange and natural treatment alternatives such as constructed wetlands and peat beds, all of which act to remove copper. However, the very low target metal concentration and highly variable outfall conditions presented a significant challenge for these treatment technologies. In addition, costs and energy use for most of these alternatives were high and secondary wastes would be generated. The Savannah River National Laboratory developed an entirely new 'detoxification' approach to treat the outfall water. This simple, lower-cost detoxification system amends outfall water with natural organic matter to bind up to 25 {micro}g/l copper rather than remove it, thereby mitigating its toxicity and protecting the sensitive species in the ecosystem. The amendments are OMRI (Organic Materials Review Institute) certified commercial products that are naturally rich in humic acids and are commonly used in organic farming.

  18. Spectroscopic characterization of dissolved organic matter isolated from rainwater.

    PubMed

    Santos, Patrícia S M; Otero, Marta; Duarte, Regina M B O; Duarte, Armando C

    2009-02-01

    Rainwater is a matrix containing extremely low concentrations (in the range of muM C) of dissolved organic carbon (DOC) and for its characterization, an efficient extraction procedure is essential. A recently developed procedure based on adsorption onto XAD-8 and XAD-4 resins in series was used in this work for the extraction and isolation of rainwater dissolved organic matter (DOM). Prior to the isolation and fractionation of DOM, and to obtain sufficient mass for the spectroscopic analyses, individual rainwater samples were batched together according to similar meteorological conditions on a total of three composed samples. The results of the isolation procedure indicated that the resin tandem procedure is not applicable for rainwater DOM since the XAD-4 resin caused samples contamination. On the other hand, the XAD-8 resin allowed DOM recoveries of 39.9-50.5% of the DOC of the original combined samples. This recovered organic fraction was characterized by UV-visible, molecular fluorescence, FTIR-ATR and 1H NMR spectroscopies. The chemical characterization of the rainwater DOM showed that the three samples consist mostly of hydroxylated and carboxylic acids with a predominantly aliphatic character, containing a minor component of aromatic structures. The obtained results suggest that the DOM in rainwater, and consequently in the precursor atmospheric particles, may have a secondary origin via the oxidation of volatile organic compounds from different origins.

  19. Iron traps terrestrially derived dissolved organic matter at redox interfaces.

    PubMed

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

    2013-06-18

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

  20. Hydrogen and carbon isotopes of petroleum and related organic matter

    NASA Astrophysics Data System (ADS)

    Yeh, Hsueh-Wen; Epstein, Samuel

    1981-05-01

    D/H and 13C /12C ratios were measured for 114 petroleum samples and for several samples of related organic matter. δD of crude oil ranges from -85 to -181‰, except for one distillate (-250‰) from the Kenai gas field; δ13C of crude oil ranges from -23.3 to -32.5‰, Variation in δD and δ13C values of compound-grouped fractions of a crude oil is small, 3 and 1.1%., respectively, and the difference in δD and δ13C between oil and coeval wax is slight. Gas fractions are 53-70 and 22.6-23.2‰ depleted in D and 13C, respectively, relative to the coexisting oil fractions. The δD and δ13C values of the crude oils appear to be largely determined by the isotopic compositions of their organic precursors. The contribution of terrestrial organic debris to the organic precursors of most marine crude oils may be significant.

  1. Organic matter loss from cultivated peat soils in Sweden

    NASA Astrophysics Data System (ADS)

    Berglund, Örjan; Berglund, Kerstin

    2015-04-01

    The degradation of drained peat soils in agricultural use is an underestimated source of loss of organic matter. Oxidation (biological degradation) of agricultural peat soils causes a loss of organic matter (OM) of 11 - 22 t ha-1 y-1 causing a CO2 emission of 20 - 40 t ha-1 y-1. Together with the associated N2O emissions from mineralized N this totals in the EU to about 98.5 Mton CO2 eq per year. Peat soils are very prone to climate change and it is expected that at the end of this century these values are doubled. The degradation products pollute surface waters. Wind erosion of peat soils in arable agriculture can cause losses of 3 - 30 t ha-1 y-1 peat also causing air pollution (fine organic particles). Subsidence rates are 1 - 2 cm per year which leads to deteriorating drainage effect and make peat soils below sea or inland water levels prone to flooding. Flooding agricultural peat soils is in many cases not possible without high costs, high GHG emissions and severe water pollution. Moreover sometimes cultural and historic landscapes are lost and meadow birds areas are lost. In areas where the possibility to regulate the water table is limited the mitigation options are either to increase biomass production that can be used as bioenergy to substitute some fossil fuel, try to slow down the break-down of the peat by different amendments that inhibit microbial activity, or permanent flooding. The negative effects of wind erosion can be mitigated by reducing wind speed or different ways to protect the soil by crops or fiber sheets. In a newly started project in Sweden a typical peat soil with and without amendment of foundry sand is cropped with reed canary grass, tall fescue and timothy to investigate the yield and greenhouse gas emissions from the different crops and how the sand effect the trafficability and GHG emissions.

  2. BiOMAS: Biochip for Organic Matter Analysis in Space

    NASA Astrophysics Data System (ADS)

    Dobrijevic, Michel; Incerti, Sebastien; Baque, Mickael; Le Postollec, Aurelie; Coussot, Gaelle; Moretto, Philippe; Vandenabeele Trambouze, Odile

    The search for the first steps of a prebiotic chemistry and the detection of life in the Solar System are ones of the great challenges of new upcoming space missions. In particular, some instruments will be designed to detect traces of organic matter on extra-terrestrial objects like Mars, Titan, comets, etc. A new and promising technique based on biochips is recommended by space agencies (ESA and NASA). A biochip is a miniaturized device composed of biological sensitive systems grafted on a slide. It allows the quantification of numerous target molecules simultaneously (from hundreds to thousands). With the support of the French space agency (CNES), our team currently develops a biochip especially designed for planetary exploration. The BiOMAS (Biochip for Organic Matter Analysis in Space) project, in progress for four years, has an interdisciplinary dimension bringing together specialists evolving in different area (planetology, physics, chemistry, biology and materials science) and developing complementary competences. A space biochip should be highly sensitive, specific and robust, allowing the detection of traces of various organic molecules (individuals and families). Since the conception of the biochip is at the heart of the instrumental specification, our aim is to optimize all the components (including the slide material, the ligands, the chemical bonds and the detection system) in order to meet both analytical and space constraints. Two different types of ligands (antibodies and aptamers) are under study to reach this objective. In space conditions, a lot of constraints might alter the efficiency of this analytical tool (irradiation by cosmic rays, temperature variations, vacuum, long duration mission, etc). Therefore, designing such a biochip requires testing the resistance of all its components to space conditions. Main concepts and current developments of the project are presented.

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

    SciTech Connect

    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.

  4. SNC Meteorites, Organic Matter and a New Look at Viking

    NASA Technical Reports Server (NTRS)

    Warmflash, David M.; Clemett, Simon J.; McKay, David S.

    2001-01-01

    Recently, evidence has begun to grow supporting the possibility that the Viking GC-MS would not have detected certain carboxylate salts that could have been present as metastable oxidation products of high molecular weight organic species. Additionally, despite the instrument's high sensitivity, the possibility had remained that very low levels of organic matter, below the instrument's detection limit, could have been present. In fact, a recent study indicates that the degradation products of several million microorganisms per gram of soil on Mars would not have been detected by the Viking GC-MS. Since the strength of the GC-MS findings was considered enough to dismiss the biology packet, particularly the LR results, any subsequent evidence suggesting that organic molecules may in fact be present on the Martian surface necessitates a re-evaluation of the Viking LR data. In addition to an advanced mass spectrometer to look for isotopic signatures of biogenic processes, future lander missions will include the ability to detect methane produced by methanogenic bacteria, as well as techniques based on biotechnology. Meanwhile, the identification of Mars samples already present on Earth in the form of the SNC meteorites has provided us with the ability to study samples of the Martian upper crust a decade or more in advance of any planned sample return missions. While contamination issues are of serious concern, the presence of indigenous organic matter in the form of polycyclic aromatic hydrocarbons has been detected in the Martian meteorites ALH84001 and Nakhla, while there is circumstantial evidence for carbonaceous material in Chassigny. The radiochronological ages of these meteorites are 4.5 Ga, 1.3 Ga, and 165 Ma respectively representing a span of time in Earth history from the earliest single-celled organisms to the present day. Given this perspective on organic material, a biological interpretation to the Viking LR results can no longer be ruled out. In the LR

  5. Molecular characterization of biodegradable dissolved organic matter using bioreactors and [12C/13C] tetramethylammonium hydroxide thermochemolysis GC-MS.

    PubMed

    Frazier, Scott W; Kaplan, Louis A; Hatcher, Patrick G

    2005-03-15

    Little is known about the molecular composition of the biodegradable fraction of dissolved organic matter (BDOM) in stream ecosystems. We combined plug-flow biofilm reactors, tetramethylammonium hydroxide (TMAH) thermochemolysis GC-MS, and 13C-labeled TMAH thermochemolysis GC-MS to study the molecular composition of BDOM from two stream ecosystems. TMAH products derived from fatty acids, lignin, and other aromatic molecules were quantified using an internal standard approach. We applied the 13C-TMAH thermochemolysis procedure to differentiate between compounds in dissolved organic matter (DOM) that had natural methoxyl groups from those that acquired methoxyl groups during the TMAH reaction. In Rio Tempisquito, a stream draining a tropical evergreen forest, and White Clay Creek, a stream draining a temperate deciduous woodlands, carbohydrates, fatty acids, and lignin contributed to the DOM and BDOM molecular composition. We observed 97 different peaks in the chromatograms of streamwater, with 57% of the peaks common to both streams. The DOM and BDOM pools from each site also contained a unique suite of compounds. Our combined use of TMAH and 13C-TMAH thermochemolysis revealed that heterotrophic bacteria can selectively degrade and demethylate different types of compounds in the lignin residues of DOM. This demonstration of bacterial demethylation of lignin, an abundant and refractory plant molecule, has potential implications for global carbon cycling.

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

    NASA Astrophysics Data System (ADS)

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

    2015-05-01

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

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

    PubMed

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

    2015-01-01

    Changes in biogeochemical cycles and the climate system due to human activities are expected to change the quantity and quality of plant litter inputs to soils. How changing quality of fresh organic matter (FOM) might influence the priming effect (PE) on soil organic matter (SOM) mineralization is still under debate. Here we determined the PE induced by two (13)C-labeled FOMs with contrasting nutritional quality (leaf vs. stalk of Zea mays L.). Soils from two different forest types yielded consistent results: soils amended with leaf tissue switched faster from negative PE to positive PE due to greater microbial growth compared to soils amended with stalks. However, after 16 d of incubation, soils amended with stalks had a higher PE than those amended with leaf. Phospholipid fatty acid (PLFA) results suggested that microbial demand for carbon and other nutrients was one of the major determinants of the PE observed. Therefore, consideration of both microbial demands for nutrients and FOM supply simultaneously is essential to understand the underlying mechanisms of PE. Our study provided evidence that changes in FOM quality could affect microbial utilization of substrate and PE on SOM mineralization, which may exacerbate global warming problems under future climate change. PMID:25960162

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

    PubMed

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

    2015-01-01

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

  9. Storage and turnover of organic matter in soil

    SciTech Connect

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

    2008-07-15

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

  10. Organic matter and metamorphic history of CO chondrites

    NASA Astrophysics Data System (ADS)

    Bonal, Lydie; Bourot-Denise, Michèle; Quirico, Eric; Montagnac, Gilles; Lewin, Eric

    2007-03-01

    The metamorphic grades of a series of eight CO3 chondrites (ALHA77307, Colony, Kainsaz, Felix, Lancé, Ornans, Warrenton and Isna) have been quantified. The method used was based on the structural grade of the organic matter trapped in the matrix, which is irreversibly transformed by thermal metamorphism. The maturation of the organic matter is independent with respect to the mineralogical context and aqueous alteration. This metamorphic tracer is thus valid whatever the chemical class of chondrites. Moreover, it is sensitive to the peak metamorphic temperature. The structural grade of the organic matter was used along with other metamorphic tracers such as petrography of opaque minerals, Fa and Fs silicate composition in type I chondrules, presolar grains and noble gas (P3 component) abundance. The deduced metamorphic hierarchy and the attributed petrographic types are the following: ALHA77307 (3.03) < Colony (3.1) < Kainsaz (3.6) < Felix (3.6 (1)) < Ornans (3.6 (2)) < Lancé (3.6 (3)) < Warrenton (3.7 (1)) < Isna (3.7 (2)). For most metamorphosed objects, the peak metamorphic temperature can be estimated using a geothermometer calibrated with terrestrial metasediments [Beyssac O., Goffe B., Chopin C., and Rouzaud J. N. (2002) Raman spectrum of carbonaceous material in metasediments: a new geothermometer. J. Metamorph. Geol., 20, 859-871]. A value of 330 °C was obtained for Allende (CV chondrite), Warrenton and Isna, consistent with temperatures estimated from Fe diffusion [Weinbruch S., Armstrong J., and Palme H. (1994). Constraints on the thermal history of the Allende parent body as derive from olivine-spinel thermometry and Fe/Mg interdiffusion in olivine. Geochim. Cosmochim. Acta58(2), 1019-1030.], from the Ni content in sulfide-metal assemblages [Zanda B., Bourot-Denise M., and Hewins R. (1995) Condensate sulfide and its metamorphic transformations in primitive chondrites. Meteorit. Planet. Sci.30, A605.] and from the d002 interlayer spacing in poorly

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

    PubMed

    Canuel, Elizabeth A; Hardison, Amber K

    2016-01-01

    Understanding the processes influencing the sources and fate of organic matter (OM) in estuaries is important for quantifying the contributions of carbon from land and rivers to the global carbon budget of the coastal ocean. Estuaries are sites of high OM production and processing, and understanding biogeochemical processes within these regions is key to quantifying organic carbon (Corg) budgets at the land-ocean margin. These regions provide vital ecological services, including nutrient filtration and protection from floods and storm surge, and provide habitat and nursery areas for numerous commercially important species. Human activities have modified estuarine systems over time, resulting in changes in the production, respiration, burial, and export of Corg. Corg in estuaries is derived from aquatic, terrigenous, and anthropogenic sources, with each source exhibiting a spectrum of ages and lability. The complex source and age characteristics of Corg in estuaries complicate our ability to trace OM along the river-estuary-coastal ocean continuum. This review focuses on the application of organic biomarkers and compound-specific isotope analyses to estuarine environments and on how these tools have enhanced our ability to discern natural sources of OM, trace their incorporation into food webs, and enhance understanding of the fate of Corg within estuaries and their adjacent waters. PMID:26407145

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

    PubMed

    Canuel, Elizabeth A; Hardison, Amber K

    2016-01-01

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

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

    NASA Astrophysics Data System (ADS)

    Canuel, Elizabeth A.; Hardison, Amber K.

    2016-01-01

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

  14. Impact of natural organic matter (NOM) on freshwater amphipods.

    PubMed

    Timofeyev, Maxim A; Wiegand, Claudia; Kent Burnison, B; Shatilina, Zhanna M; Pflugmacher, Stephan; Steinberg, Christian E W

    2004-02-01

    Natural organic matter (NOM) isolated from the eutrophic Sanctuary Pond (Point Pelee National Park, Canada) has an adverse impact on amphipod species (Gammarus tigrinus and Chaetogammarus ischnus from Lake Müggelsee, Germany, and Eulimnogammarus cyaneus, from Lake Baikal, Russia). Increases in amphipod mortality, changes in peroxidase activity and increases of heat shock protein (hsp70) expression were observed upon exposure to NOM. The highest resistance to the adverse impact of NOM was observed with the endemic Baikalian amphipod E. cyaneus. However, the mechanisms behind this finding remains obscure. If differences in the sensitivity of the hsp70 antibody may be excluded, different modes of action may be postulated: because the adverse impact of NOM may be caused by reactive oxygen species (ROS) and the NOM itself, the observed differences may be due to the action of ROS alone (with E. cyaneus) and a combination of both adverse modes of action (European species). PMID:14967505

  15. Modeling of natural organic matter transport processes in groundwater.

    PubMed Central

    Yeh, T C; Mas-Pla, J; McCarthy, J F; Williams, T M

    1995-01-01

    A forced-gradient tracer test was conducted at the Georgetown site to study the transport of natural organic matter (NOM) in groundwater. In particular, the goal of this experiment was to investigate the interactions between NOM and the aquifer matrix. A detailed three-dimensional characterization of the hydrologic conductivity heterogeneity of the site was obtained using slug tests. The transport of a conservative tracer (chloride) was successfully reproduced using these conductivity data. Despite the good simulation of the flow field, NOM breakthrough curves could not be reproduced using a two-site sorption model with spatially constant parameters. Preliminary results suggest that different mechanisms for the adsorption/desorption processes, as well as their spatial variability, may significantly affect the transport and fate of NOM. PMID:7621798

  16. [Dissolved organic matter (DOM) dynamics in karst aquifer systems].

    PubMed

    Yao, Xin; Zou, Sheng-Zhang; Xia, Ri-Yuan; Xu, Dan-Dan; Yao, Min

    2014-05-01

    Dissolved organic matter (DOM) and nutrients have a unique way of producing, decomposing and storing in southwest karst water systems. To understand the biogeochemical cycle of DOM in karst aquifer systems, we investigated the behavioral changes of DOM fluorescence components in Zhaidi karst river system. Two humic-like components (C1 and C2), and one autochthonous tyrosine-like component (C4) were identified using the parallel factor analysis (PARAFAC) model. Compared with the traditional physical and chemical indicators, spatial heterogeneity of DOM was more obvious, which can reflect the subtle changes in groundwater system. Traditional indicators mainly reflect the regional characteristics of karst river system, while DOM fluorescence components reflect the attribute gaps of sampling types.

  17. Systematic approaches to comprehensive analyses of natural organic matter

    USGS Publications Warehouse

    Leenheer, Jerry A.

    2009-01-01

    The more that is learned of the chemistry of aquatic natural organic matter (NOM) the greater is the scientific appreciation of the vast complexity of this subject. This complexity is due not only to a multiplicity of precursor molecules in any environment but to their associations with each other and with other components of local environments such as clays, mineral acids and dissolved metals. In addition, this complex system is subject to constant change owing to environmental variables and microbial action. Thus, there is a good argument that no two NOM samples are exactly the same even from the same source at nearly the same time. When ubiquity of occurrence, reaction with water treatment chemicals, and subsequent human exposure are added to the list of NOM issues, one can understand the appeal that this subject holds for a wide variety of environmental scientists.

  18. New monoaromatic steroids in organic matter of the apocatagenesis zone

    NASA Astrophysics Data System (ADS)

    Kashirtsev, V. A.; Fomin, A. N.; Shevchenko, N. P.; Dolzhenko, K. V.

    2016-08-01

    According to the materials of geochemical study in the core of the ultradeep hole SV-27 of aromatic fractions of bitumoids of the Vilyui syneclise (East Siberia) by the method of chromatography-mass spectrometry, starting from the depth of >5000 m, four diastereomers of previously unknown hydrocarbons, which become predominant in the fraction at a depth of ˜6500 m, were distinguished. Similar hydrocarbons were found in organic matter of Upper Paleozoic rocks of the Kharaulakh anticlinorium in the Verkhoyansk folded area. According to the intense molecular ion m/z 366 and the character of the basic fragmental ions (m/z 238, 309, and 323), the major structure of the compounds studied was determined as 17-desmethyl-23-methylmonoaromatic steroid C27. The absence of such steroids in oil of the Vilyui syneclise shows that deep micro-oils did not participate in the formation of oil fringes of gas condensate deposits of the region.

  19. A search for presolar organic matter in meteorite

    NASA Technical Reports Server (NTRS)

    Yang, J.; Epstein, S.

    1985-01-01

    The D/H ratios and the C-13/C-12 ratios of acid-insoluble organic matter of 4 meteorites, Ochansk (H4), Plainview (H5), Gladstone (H6) and Odessa (IA), were measured. delta-D values for hydrogen extracted by stepwise combustion were negative, down to -280 deg/infinity. delta-C-13 values were also negative except in the case of the carbon coming off at the highest temperature steps for Plainview and Odessa meteorites. The concentrations of C-13-rich carbon were 3-5 orders of magnitude smaller than those found in Murchison meteorite, suggesting that relic grains of stellar condensates were mostly destroyed in the meteorites examined.

  20. Grown organic matter as a fuel raw material resource

    NASA Technical Reports Server (NTRS)

    Roller, W. L.; Keener, H. M.; Kline, R. D.; Mederski, H. J.; Curry, R. B.

    1975-01-01

    An extensive search was made on biomass production from the standpoint of climatic zones, water, nutrients, costs and energy requirements for many species. No exotic species were uncovered that gave hope for a bonanza of biomass production under culture, location, and management markedly different from those of existing agricultural concepts. A simulation analysis of biomass production was carried out for six species using conventional production methods, including their production costs and energy requirements. These estimates were compared with data on food, fiber, and feed production. The alternative possibility of using residues from food, feed, or lumber was evaluated. It was concluded that great doubt must be cast on the feasibility of producing grown organic matter for fuel, in competition with food, feed, or fiber. The feasibility of collecting residues may be nearer, but the competition for the residues for return to the soil or cellulosic production is formidable.

  1. Priming-induced Changes in Permafrost Soil Organic Matter Decomposition

    NASA Astrophysics Data System (ADS)

    Pegoraro, E.; Schuur, E.; Bracho, R. G.

    2015-12-01

    Warming of tundra ecosystems due to climate change is predicted to thaw permafrost and increase plant biomass and litter input to soil. Additional input of easily decomposable carbon can alter microbial activity by providing a much needed energy source, thereby accelerating soil organic matter decomposition. This phenomenon, known as the priming effect, can increase CO2 flux from soil to the atmosphere. However, the extent to which this mechanism can decrease soil carbon stocks in the Arctic is unknown. This project assessed priming effects on permafrost soil collected from a moist acidic tundra site in Healy, Alaska. We hypothesized that priming would increase microbial activity by providing microbes with a fresh source of carbon, thereby increasing decomposition of old and slowly decomposing carbon. Soil from surface and deep layers were amended with multiple pulses of uniformly 13C labeled glucose and cellulose, and samples were incubated at 15° C to quantify whether labile substrate addition increased carbon mineralization. We quantified the proportion of old carbon mineralization by measuring 14CO2. Data shows that substrate addition resulted in higher respiration rates in amended soils; however, priming was only observed in deep layers, where 30% more soil-derived carbon was respired compared to control samples. This suggests that microbes in deep layers are limited in energy, and the addition of labile carbon increases native soil organic matter decomposition, especially in soil with greater fractions of slowly decomposing carbon. Priming in permafrost could exacerbate the effects of climate change by increasing mineralization rates of carbon accumulated over the long-term in deep layers. Therefore, quantifying priming effect in permafrost soils is imperative to understanding the dynamics of carbon turnover in a warmer world.

  2. Effects of warming on stream biofilm organic matter use capabilities.

    PubMed

    Ylla, Irene; Canhoto, Cristina; Romaní, Anna M

    2014-07-01

    The understanding of ecosystem responses to changing environmental conditions is becoming increasingly relevant in the context of global warming. Microbial biofilm communities in streams play a key role in organic matter cycling which might be modulated by shifts in flowing water temperature. In this study, we performed an experiment at the Candal stream (Portugal) longitudinally divided into two reaches: a control half and an experimental half where water temperature was 3 °C above that of the basal stream water. Biofilm colonization was monitored during 42 days in the two stream halves. Changes in biofilm function (extracellular enzyme activities and carbon substrate utilization profiles) as well as chlorophyll a and prokaryote densities were analyzed. The biofilm in the experimental half showed a higher capacity to decompose cellulose, hemicellulose, lignin, and peptidic compounds. Total leucine-aminopeptidase, cellobiohydrolase and β-xylosidase showed a respective 93, 66, and 61% increase in activity over the control; much higher than would be predicted by only the direct temperature physical effect. In contrast, phosphatase and lipase activity showed the lowest sensitivity to temperature. The biofilms from the experimental half also showed a distinct functional fingerprint and higher carbon usage diversity and richness, especially due to a wider use of polymers and carbohydrates. The changes in the biofilm functional capabilities might be indirectly affected by the higher prokaryote and chlorophyll density measured in the biofilm of the experimental half. The present study provides evidence that a realistic stream temperature increase by 3 °C changes the biofilm metabolism to a greater decomposition of polymeric complex compounds and peptides but lower decomposition of lipids. This might affect stream organic matter cycling and the transfer of carbon to higher trophic levels.

  3. Ocean warming-acidification synergism undermines dissolved organic matter assembly.

    PubMed

    Chen, Chi-Shuo; Anaya, Jesse M; Chen, Eric Y-T; Farr, Erik; Chin, Wei-Chun

    2015-01-01

    Understanding the influence of synergisms on natural processes is a critical step toward determining the full-extent of anthropogenic stressors. As carbon emissions continue unabated, two major stressors--warming and acidification--threaten marine systems on several scales. Here, we report that a moderate temperature increase (from 30°C to 32°C) is sufficient to slow--even hinder--the ability of dissolved organic matter, a major carbon pool, to self-assemble to form marine microgels, which contribute to the particulate organic matter pool. Moreover, acidification lowers the temperature threshold at which we observe our results. These findings carry implications for the marine carbon cycle, as self-assembled marine microgels generate an estimated global seawater budget of ~1016 g C. We used laser scattering spectroscopy to test the influence of temperature and pH on spontaneous marine gel assembly. The results of independent experiments revealed that at a particular point, both pH and temperature block microgel formation (32°C, pH 8.2), and disperse existing gels (35°C). We then tested the hypothesis that temperature and pH have a synergistic influence on marine gel dispersion. We found that the dispersion temperature decreases concurrently with pH: from 32°C at pH 8.2, to 28°C at pH 7.5. If our laboratory observations can be extrapolated to complex marine environments, our results suggest that a warming-acidification synergism can decrease carbon and nutrient fluxes, disturbing marine trophic and trace element cycles, at rates faster than projected.

  4. Ocean warming-acidification synergism undermines dissolved organic matter assembly.

    PubMed

    Chen, Chi-Shuo; Anaya, Jesse M; Chen, Eric Y-T; Farr, Erik; Chin, Wei-Chun

    2015-01-01

    Understanding the influence of synergisms on natural processes is a critical step toward determining the full-extent of anthropogenic stressors. As carbon emissions continue unabated, two major stressors--warming and acidification--threaten marine systems on several scales. Here, we report that a moderate temperature increase (from 30°C to 32°C) is sufficient to slow--even hinder--the ability of dissolved organic matter, a major carbon pool, to self-assemble to form marine microgels, which contribute to the particulate organic matter pool. Moreover, acidification lowers the temperature threshold at which we observe our results. These findings carry implications for the marine carbon cycle, as self-assembled marine microgels generate an estimated global seawater budget of ~1016 g C. We used laser scattering spectroscopy to test the influence of temperature and pH on spontaneous marine gel assembly. The results of independent experiments revealed that at a particular point, both pH and temperature block microgel formation (32°C, pH 8.2), and disperse existing gels (35°C). We then tested the hypothesis that temperature and pH have a synergistic influence on marine gel dispersion. We found that the dispersion temperature decreases concurrently with pH: from 32°C at pH 8.2, to 28°C at pH 7.5. If our laboratory observations can be extrapolated to complex marine environments, our results suggest that a warming-acidification synergism can decrease carbon and nutrient fluxes, disturbing marine trophic and trace element cycles, at rates faster than projected. PMID:25714090

  5. Response of Dissolved Organic Matter to Warming and Nitrogen Addition

    NASA Astrophysics Data System (ADS)

    Choi, J. H.; Nguyen, H.

    2014-12-01

    Dissolved Organic Matter (DOM) is a ubiquitous mixture of soluble organic components. Since DOM is produced from the terrestrial leachate of various soil types, soil may influence the chemistry and biology of freshwater through the input of leachate and run-off. The increased temperature by climate change could dramatically change the DOM characteristics of soils through enhanced decomposition rate and losses of carbon from soil organic matter. In addition, the increase in the N-deposition affects DOM leaching from soils by changing the carbon cycling and decomposition rate of soil decay. In this study, we conducted growth chamber experiments using two types of soil (wetland and forest) under the conditions of temperature increase and N-deposition in order to investigate how warming and nitrogen addition influence the characteristics of the DOM leaching from different soil types. This leachate controls the quantity and quality of DOM in surface water systems. After 10 months of incubation, the dissolved organic carbon (DOC) concentrations decreased for almost samples in the range of 7.6 to 87.3% (ANOVA, p<0.05). The specific UV absorption (SUVA) values also decreased for almost samples after the first 3 months and then increased gradually afterward in range of 3.3 to 108.4%. Both time and the interaction between time and the temperature had the statistically significant effects on the SUVA values (MANOVA, p<0.05). Humification index (HIX) showed the significant increase trends during the duration of incubation and temperature for almost the samples (ANOVA, p<0.05). Higher decreases in the DOC values and increases in HIX were observed at higher temperatures, whereas the opposite trend was observed for samples with N-addition. The PARAFAC results showed that three fluorescence components: terrestrial humic (C1), microbial humic-like (C2), and protein-like (C3), constituted the fluorescence matrices of soil samples. During the experiment, labile DOM from the soils was

  6. Reactivity of Pleistocene aged organic matter in the Siberian Arctic

    NASA Astrophysics Data System (ADS)

    Davydov, S.; Vonk, J. E.; Mann, P. J.; Davydova, A.; Sobczak, W. V.; Schade, J. D.; Bulygina, E. B.; Zimov, S. A.; Holmes, R. M.

    2011-12-01

    -normalized O2 losses demonstrated a different pattern. After a 24h C-loss of 5-7% for all three dilutions, the 10% dilution continued to respond up to a total of 33% lost carbon after 5 days. Enzymatic activity rates of the lignin-degrading enzyme phenoloxidase corroborated this by showing strongly elevated activity rates for the 10% Duvannyi Yar-Kolyma dilution, opposite to the 1% or 0.5% dilutions or Kolyma background. Dilutions with Kolyma water showed a slightly but consistently higher processing rate compared to dilutions of East Siberian Sea water (26 salinity). These results suggest that old OC is biologically labile upon fluvial release and its breakdown appears to be limited by availability of organic substrates. Furthermore, it appears that refractory carbon in the Kolyma is in fact being processed faster when enough Duvannyi Yar water, along with its microbes and enzymes, is added.

  7. Organic matter cycling across the sulfate-methane transition zone of the Santa Barbara Basin, California Borderland

    NASA Astrophysics Data System (ADS)

    Komada, Tomoko; Burdige, David J.; Li, Huan-Lei; Magen, Cédric; Chanton, Jeffrey P.; Cada, Abraham K.

    2016-03-01

    Consumption of sulfate (SO42-) in the sulfate-methane transition zone (SMTZ) has often been considered to be due solely to anaerobic oxidation of methane (AOM). However, recent studies show SO42- fluxes into the SMTZ that exceed methane (CH4) fluxes, thereby challenging this conceptual model. Co-occurrence of organoclastic SO42- reduction (oSR) with AOM in the SMTZ has been hypothesized to be the cause for this flux imbalance, but conclusive evidence is lacking. To address this knowledge gap, we investigated organic matter cycling in the SMTZ of the organic-rich sediments of the Santa Barbara Basin, California Borderland, and examined the occurrence of oSR within this zone using bulk solute profiles and Δ14C and δ13C values of selected carbon pools. We also tested the hypothesis that the SMTZ acts as an oxidation front not just for CH4, but also for dissolved organic carbon (DOC) that is produced below the SMTZ and migrates upward. Mass balance calculations for the SMTZ based on reaction stoichiometry and Δ14C and δ13C values of associated carbon fluxes indicate that ∼35-45% of total SO42- reduction in the SMTZ occurs via oSR, with the remainder attributable to AOM. The δ13C value of net DOC production is distinct from that of the fraction of bulk POC undergoing degradation, suggesting that pore-water DOC represents a compositionally unique slice of the metabolizable POC pool. DOC diffusing upward at 450 cm is virtually free of 14C and contain low levels of short-chain organic acids. Radiocarbon mass balance shows that >30% of this pre-aged, and presumably refractory, DOC is removed from the pore waters within or immediately below the SMTZ. Although the SMTZ does not appear to be a major net DOC oxidation front, these results show that DOC dynamics provide unique insights into organic matter processing in these subsurface sediments.

  8. Soil organic matter and the extracellular microbial matrix show contrasting responses to C and N availability

    PubMed Central

    Redmile-Gordon, M.A.; Evershed, R.P.; Hirsch, P.R.; White, R.P.; Goulding, K.W.T.

    2015-01-01

    An emerging paradigm in soil science suggests microbes can perform ‘N mining’ from recalcitrant soil organic matter (SOM) in conditions of low N availability. However, this requires the production of extracellular structures rich in N (including enzymes and structural components) and thus defies stoichiometric expectation. We set out to extract newly synthesised peptides from the extracellular matrix in soil and compare the amino acid (AA) profiles, N incorporation and AA dynamics in response to labile inputs of contrasting C/N ratio. Glycerol was added both with and without an inorganic source of N (10% 15N labelled NH4NO3) to a soil already containing a large pool of refractory SOM and incubated for 10 days. The resulting total soil peptide (TSP) and extracellular pools were compared using colorimetric methods, gas chromatography, and isotope ratio mass spectrometry. N isotope compositions showed that the extracellular polymeric substance (EPS) contained a greater proportion of products formed de novo than did TSP, with hydrophobic EPS-AAs (leucine, isoleucine, phenylalanine, hydroxyproline and tyrosine) deriving substantially more N from the inorganic source provided. Quantitative comparison between extracts showed that the EPS contained greater relative proportions of alanine, glycine, proline, phenylalanine and tyrosine. The greatest increases in EPS-peptide and EPS-polysaccharide concentrations occurred at the highest C/N ratios. All EPS-AAs responded similarly to treatment whereas the responses of TSP were more complex. The results suggest that extracellular investment of N (as EPS peptides) is a microbial survival mechanism in conditions of low N/high C which, from an evolutionary perspective, must ultimately lead to the tendency for increased N returns to the microbial biomass. A conceptual model is proposed that describes the dynamics of the extracellular matrix in response to the C/N ratio of labile inputs. PMID:26339106

  9. Geochemical drivers of organic matter decomposition in Arctic tundra soils

    SciTech Connect

    Herndon, Elizabeth M.; Yang, Ziming; Graham, David E.; Wullschleger, Stan D.; Gu, Baohua; Liang, Liyuan; Bargar, John; Janot, Noemie; Regier, Tom Z.

    2015-12-07

    Climate change is warming tundra ecosystems in the Arctic, resulting in the decomposition of previously-frozen soil organic matter (SOM) and release of carbon (C) to the atmosphere; however, the processes that control SOM decomposition and C emissions remain highly uncertain. In this study, we evaluate geochemical factors that influence anaerobic production of carbon dioxide (CO2) and methane (CH4) in the active layers of four ice-wedge polygons. Surface and soil pore waters were collected during the annual thaw season over a two-year period in an area containing waterlogged, low-centered polygons and well-drained, high-centered polygons. We report spatial and seasonal patterns of dissolved gases in relation to the geochemical properties of Fe and organic C as determined using spectroscopic and chromatographic techniques. Iron was present as Fe(II) in soil solution near the permafrost boundary but enriched as Fe(III) in the middle of the active layer, similar to dissolved aromatic-C and organic acids. Dissolved CH4 increased relative to dissolved CO2 with depth and varied with soil moisture in the middle of the active layer in patterns that were positively correlated with the proportion of dissolved Fe(III) in transitional and low-centered polygon soils but negatively correlated in the drier flat- and high-centered polygons. These results suggest that microbial-mediated Fe oxidation and reduction influence respiration/fermentation of SOM and production of substrates (e.g., low-molecular-weight organic acids) for methanogenesis. As a result, we infer that geochemical differences induced by water saturation dictate microbial products of SOM decomposition, and Fe geochemistry is an important factor regulating methanogenesis in anoxic tundra soils.

  10. Geochemical drivers of organic matter decomposition in Arctic tundra soils

    DOE PAGESBeta

    Herndon, Elizabeth M.; Yang, Ziming; Graham, David E.; Wullschleger, Stan D.; Gu, Baohua; Liang, Liyuan; Bargar, John; Janot, Noemie; Regier, Tom Z.

    2015-12-07

    Climate change is warming tundra ecosystems in the Arctic, resulting in the decomposition of previously-frozen soil organic matter (SOM) and release of carbon (C) to the atmosphere; however, the processes that control SOM decomposition and C emissions remain highly uncertain. In this study, we evaluate geochemical factors that influence anaerobic production of carbon dioxide (CO2) and methane (CH4) in the active layers of four ice-wedge polygons. Surface and soil pore waters were collected during the annual thaw season over a two-year period in an area containing waterlogged, low-centered polygons and well-drained, high-centered polygons. We report spatial and seasonal patterns ofmore » dissolved gases in relation to the geochemical properties of Fe and organic C as determined using spectroscopic and chromatographic techniques. Iron was present as Fe(II) in soil solution near the permafrost boundary but enriched as Fe(III) in the middle of the active layer, similar to dissolved aromatic-C and organic acids. Dissolved CH4 increased relative to dissolved CO2 with depth and varied with soil moisture in the middle of the active layer in patterns that were positively correlated with the proportion of dissolved Fe(III) in transitional and low-centered polygon soils but negatively correlated in the drier flat- and high-centered polygons. These results suggest that microbial-mediated Fe oxidation and reduction influence respiration/fermentation of SOM and production of substrates (e.g., low-molecular-weight organic acids) for methanogenesis. As a result, we infer that geochemical differences induced by water saturation dictate microbial products of SOM decomposition, and Fe geochemistry is an important factor regulating methanogenesis in anoxic tundra soils.« less

  11. Adsorption of paraquat on soil organic matter: effect of exchangeable cations and dissolved organic carbon.

    PubMed

    Gondar, Dora; López, Rocío; Antelo, Juan; Fiol, Sarah; Arce, Florencio

    2012-10-15

    Herbicides that interact with soil organic matter do so with both the solid and the dissolved fractions, so that the distribution of herbicide between the soil solution and solid phases is determined by competitive effects. In the present study, adsorption experiments were carried out with the cationic herbicide paraquat and untreated and acid-washed samples of a peat soil, at different values of pH and ionic strength. Less herbicide was adsorbed onto the untreated peat than onto the acid-washed peat; the difference was due to the presence of exchangeable cations, as demonstrated in experiments carried out by adding Ca(2+) to suspensions of acid-washed peat. The results were interpreted by an electrostatic model and the fitting parameters indicated that the adsorption constants were the same for both samples of peat, although the number of binding sites available was different. Simultaneous resolution of the adsorption equilibrium of paraquat for the soil organic matter (SOM) and of the binding equilibrium between paraquat and dissolved organic matter (DOM) enabled the distribution of paraquat between the solid and solution phases to be determined. The increased solubility of the SOM with increasing pH led to a decrease in the fraction of paraquat retained on the peat surface above pH 5.5, which favors the mobility of the herbicide in the soil.

  12. Partition of nonpolar organic pollutants from water to soil and sediment organic matters

    USGS Publications Warehouse

    Chiou, C.T.

    1995-01-01

    The partition coefficients (Koc) of carbon tetrachloride and 1,2-dichlorobenzene between normal soil/sediment organic matter and water have been determined for a large set of soils, bed sediments, and suspended solids from the United States and the People's Republic of China. The Koc values for both solutes are quite invariant either for the soils or for the bed sediments; the values on bed sediments are about twice those on soils. The similarity of Koc values between normal soils and between normal bed sediments suggests that natural organic matters in soils (or sediments) of different geographic origins exhibit comparable polarities and possibly comparable compositions. The results also suggest that the process that converts eroded soils into bed sediments brings about a change in the organic matter property. The difference between soil and sediment Koc values provides a basis for identifying the source of suspended solids in river waters. The very high Koc values observed for some special soils and sediments are diagnostic of severe anthropogenic contamination.

  13. Solid organic matter in the atmosphere and on the surface of outer Solar System bodies.

    PubMed

    Khare, B N; Bakes, E L; Cruikshank, D; McKay, C P

    2001-01-01

    Many bodies in the outer Solar System display the presence of low albedo materials. These materials, evident on the surface of asteroids, comets, Kuiper Belt objects and their intermediate evolutionary step, Centaurs, are related to macromolecular carbon bearing materials such as polycyclic aromatic hydrocarbons and organic materials such as methanol and related light hydrocarbons, embedded in a dark, refractory, photoprocessed matrix. Many planetary rings and satellites around the outer gaseous planets display such component materials. One example, Saturn's largest satellite, Titan, whose atmosphere is comprised of around 90% molecular nitrogen N2 and less than 10% methane CH4, displays this kind of low reflectivity material in its atmospheric haze. These materials were first recorded during the Voyager 1 and 2 flybys of Titan and showed up as an optically thick pinkish orange haze layer. These materials are broadly classified into a chemical group whose laboratory analogs are termed "tholins", after the Greek word for "muddy". Their analogs are produced in the laboratory via the irradiation of gas mixtures and ice mixtures by radiation simulating Solar ultraviolet (UV) photons or keV charged particles simulating particles trapped in Saturn's magnetosphere. Fair analogs of Titan tholin are produced by bombarding a 9:1 mixture of N2:CH4 with charged particles and its match to observations of both the spectrum and scattering properties of the Titan haze is very good over a wide range of wavelengths. In this paper, we describe the historical background of laboratory research on this kind of organic matter and how our laboratory investigations of Titan tholin compare. We comment on the probable existence of polycyclic aromatic hydrocarbons in the Titan Haze and how biological and nonbiological racemic amino acids produced from the acid hydrolysis of Titan tholins make these complex organic compounds prime candidates in the evolution of terrestrial life and

  14. Removal of bromide and natural organic matter by anion exchange.

    PubMed

    Hsu, Susan; Singer, Philip C

    2010-04-01

    Bromide removal by anion exchange was explored for various water qualities, process configurations, and resin characteristics. Simulated natural waters containing different amounts of natural organic matter (NOM), bicarbonate, chloride, and bromide were treated with a polyacrylate-based magnetic ion exchange (MIEX) resin on a batch basis to evaluate the effectiveness of the resin for removal of bromide. While bromide removal was achieved to some degree, alkalinity (bicarbonate), dissolved organic carbon (DOC), and chloride were shown to inhibit bromide removal in waters with bromide concentrations of 100 and 300 microg/L. Water was also treated using a two-stage batch MIEX process. Two-stage treatment resulted in only a slight improvement in bromide removal compared to single-stage treatment, presumably due to competition with the high concentration of chloride which is present along with bromide in natural waters. In view of the relatively poor bromide removal results for the MIEX resin, a limited set of experiments was performed using polystyrene resins. DOC and bromide removal were compared by treating model waters with MIEX and two polystyrene resins, Ionac A-641 and Amberlite IRA910. The two polystyrene resins were seen to be more effective for bromide removal, while the MIEX resin was more effective at removing DOC.

  15. Precipitates in landfill leachate mediated by dissolved organic matters.

    PubMed

    Li, Zhenze; Xue, Qiang; Liu, Lei; Li, Jiangshan

    2015-04-28

    Clogging of landfill leachate collection system is so ubiquitous that it causes problems to landfills. Although precipitations of calcite and other minerals have been widely observed, the mechanism of precipitation remains obscure. We examined the clog composition, dissolved organic matters, leachate chemical compositions and the correlation of these variables in view of the precipitation process. It is shown that Dissolved Organic Carbon (DOC) inhibits precipitation of landfill leachate. Using the advanced NICA-Donnan model, the analysis of aqueous chemical reactions between Mg-Ca-DOC-CO2 suggests a good agreement with experimental observations. Calcite and dolomite are both found to be oversaturated in most of the landfill leachate samples. DOC is found to preferentially bind with Mg than Ca, leading to more likely precipitation of Calcite than dolomite from landfill leachate. The NICA-Donnan model gives a reasonable estimation of dolomite saturation index in a wide range of DOC. Modeling confirms the major precipitation mechanism in terms of alkaline earth metal carbonate. Uncertainties in model parameters are discussed with particular focus on DOC composition, functional group types and density concentration and the influential factors. PMID:25661175

  16. Transformation of organic matters in animal wastes during composting.

    PubMed

    Wang, Ke; He, Chao; You, Shijie; Liu, Weijie; Wang, Wei; Zhang, Ruijun; Qi, Huanhuan; Ren, Nanqi

    2015-12-30

    The transformation of organic matters in swine, cow and chicken manures was compared and evaluated using elemental analysis, FTIR, (13)C NMR, pyrolysis/GC/MS, Biolog and multiple fluorochrome over 60 days composting. The results revealed that cow manure exhibited the greatest C/N and aromaticity, whereas chicken manure exhibited the highest nitrogen and sulfur contents. O-alkyl-C was predominant carbon structure in the three manures. Alkyl-C and carboxyl-C were decomposed dramatically in initial 10 days, and mineralization of O-alkyl-C dominated the curing stage. During pyrolysis of chicken, cow, and swine manures, the majority products were fatty acids, phenols and cholestene derivatives, respectively, however, phenols and cholestene derivatives were strongly reduced in the mature manures. Furthermore, microorganisms in the raw cow, chicken and swine manure demonstrated the highest degradation capabilities for carbohydrates, lipids and amino acids, respectively. Spatial differences in the contents of solid organics in the manure particles were negligible through detection by multiple staining methods during composting.

  17. Effects of pressure on thermal evolution of organic matter

    SciTech Connect

    Goffe, B.; Domine, F. )

    1989-09-01

    In the internal metamorphic zones of the French Alps, organic matter-bearing terrestrial sediments of Dogger age underwent an Eocene high-pressure metamorphic event (607 kbar at 300{degree}-330{degree}C). These metasediments now contain, trapped in metamorphic minerals, low evolved kerogen (small extent of molecular orientation), heavy hydrocarbon compounds (aromatic and aliphatic up to C{sup 30} with traces of pristane and phytane molecules), and gases with low C{sup 1}/C{sup 2}-C{sup 6} ratios. However, the degree of organic maturation (equivalent to catagenesis) is much less than that predicted by classical models. This field example indicates that the oil window opens with increasing pressure. Experimental pyrolysis of supercritical hexane performed in a closed, constant-pressure gold reactor at 210-15,600 bars pressure range and 290{degree}-365{degree}C, clearly demonstrates the important influence of pressure on the product distribution of hexane pyrolysis: as pressure is increased, relative light product yields decrease and heavy products increase. This can be interpreted mainly by considering the activation volumes of the reactions involved. In conclusion, the experimental and natural examples presented here indicate that the rate of thermal maturation decreases with pressure.

  18. Transformation of organic matters in animal wastes during composting.

    PubMed

    Wang, Ke; He, Chao; You, Shijie; Liu, Weijie; Wang, Wei; Zhang, Ruijun; Qi, Huanhuan; Ren, Nanqi

    2015-12-30

    The transformation of organic matters in swine, cow and chicken manures was compared and evaluated using elemental analysis, FTIR, (13)C NMR, pyrolysis/GC/MS, Biolog and multiple fluorochrome over 60 days composting. The results revealed that cow manure exhibited the greatest C/N and aromaticity, whereas chicken manure exhibited the highest nitrogen and sulfur contents. O-alkyl-C was predominant carbon structure in the three manures. Alkyl-C and carboxyl-C were decomposed dramatically in initial 10 days, and mineralization of O-alkyl-C dominated the curing stage. During pyrolysis of chicken, cow, and swine manures, the majority products were fatty acids, phenols and cholestene derivatives, respectively, however, phenols and cholestene derivatives were strongly reduced in the mature manures. Furthermore, microorganisms in the raw cow, chicken and swine manure demonstrated the highest degradation capabilities for carbohydrates, lipids and amino acids, respectively. Spatial differences in the contents of solid organics in the manure particles were negligible through detection by multiple staining methods during composting. PMID:26311195

  19. Chromophoric dissolved organic matter export from U.S. rivers

    NASA Astrophysics Data System (ADS)

    Spencer, Robert G. M.; Aiken, George R.; Dornblaser, Mark M.; Butler, Kenna D.; Holmes, R. Max; Fiske, Greg; Mann, Paul J.; Stubbins, Aron

    2013-04-01

    Chromophoric dissolved organic matter (CDOM) fluxes and yields from 15 major U.S. rivers draining an assortment of terrestrial biomes are presented. A robust relationship between CDOM and dissolved organic carbon (DOC) loads is established (e.g., a350 versus DOC; r2 = 0.96, p < 0.001). Calculated CDOM yields are also correlated to watershed percent wetland (e.g. a350; r2 = 0.81, p < 0.001) providing a method for the estimation of CDOM export from ungauged watersheds. A large variation in CDOM yields was found across the rivers. The two rivers in the north-eastern U.S. (Androscoggin and Penobscot), the Edisto draining into the South Atlantic Bight, and some rivers draining into the Gulf of Mexico (Atchafalaya and Mobile) exhibit the highest CDOM yields, linked to extensive wetlands in these watersheds. If the Edisto CDOM yield is representative of other rivers draining into the South Atlantic Bight, this would result in a CDOM load equivalent to that of the Mississippi from a region of approximately 10% of the Mississippi watershed, indicating the importance of certain regions with respect to the role of terrigenous CDOM in ocean color budgets.

  20. Chromophoric Dissolved Organic Matter Export from U.S. Rivers

    NASA Astrophysics Data System (ADS)

    Spencer, R. G.; Aiken, G.; Dornblaser, M.; Butler, K. D.; Holmes, R. M.; Fiske, G.; Mann, P. J.; Stubbins, A.

    2012-12-01

    Chromophoric dissolved organic matter (CDOM) fluxes and yields from 15 major U.S. rivers draining an assortment of terrestrial biomes are presented. Utilizing CDOM and dissolved organic carbon (DOC) flux data we establish a robust universal relationship between CDOM and DOC loads. The application of this relationship allows future studies to derive DOC loads from CDOM utilizing emerging in-situ or remote sensing technologies and thus refine river-to-ocean DOC fluxes, as well as exploit historic imagery to examine how fluxes may have changed. Calculated CDOM yields from the 15 U.S. rivers highlight the importance of certain regions with respect to CDOM flux to the coastal ocean. This approach indicates that future studies might predict CDOM and DOC yields for different watershed types that could then be readily converted to loads providing for the estimation of CDOM and DOC export from ungauged watersheds. Examination of CDOM yields also highlights important geographical regions for future study with respect to the role of terrigenous CDOM in ocean color budgets and CDOM's role in biogeochemical processes.

  1. Toward an experimental synthesis of the chondritic insoluble organic matter

    NASA Astrophysics Data System (ADS)

    Biron, Kasia; Derenne, Sylvie; Robert, FrançOis; Rouzaud, Jean-NoëL.

    2015-08-01

    Based on the statistical model proposed for the molecular structure of the insoluble organic matter (IOM) isolated from the Murchison meteorite, it was recently proposed that, in the solar T-Tauri disk regions where (photo)dissociation of gaseous molecules takes place, aromatics result from the cyclization/aromatization of short aliphatics. This hypothesis is tested in this study, with n-alkanes being submitted to high-frequency discharge at low pressure. The contamination issue was eliminated using deuterated precursor. IOM was formed and studied using solid-state nuclear magnetic resonance, pyrolysis coupled to gas chromatography and mass spectrometry, RuO4 oxidation, and high-resolution transmission electron microscopy. It exhibits numerous similarities at the molecular level with the hydrocarbon backbone of the natural IOM, reinforcing the idea that the initial precursors of the IOM were originally chains in the gas. Moreover, a fine comparison between the chemical structure of several meteorite IOM suggests either that (i) the meteorite IOMs share a common precursor standing for the synthetic IOM or that (ii) the slight differences between the meteorite IOMs reflect differences in their environment at the time of their formation i.e., related to plasma temperature that, in turn, dictates the dissociation-recombination rates of organic fragments.

  2. Precipitates in landfill leachate mediated by dissolved organic matters.

    PubMed

    Li, Zhenze; Xue, Qiang; Liu, Lei; Li, Jiangshan

    2015-04-28

    Clogging of landfill leachate collection system is so ubiquitous that it causes problems to landfills. Although precipitations of calcite and other minerals have been widely observed, the mechanism of precipitation remains obscure. We examined the clog composition, dissolved organic matters, leachate chemical compositions and the correlation of these variables in view of the precipitation process. It is shown that Dissolved Organic Carbon (DOC) inhibits precipitation of landfill leachate. Using the advanced NICA-Donnan model, the analysis of aqueous chemical reactions between Mg-Ca-DOC-CO2 suggests a good agreement with experimental observations. Calcite and dolomite are both found to be oversaturated in most of the landfill leachate samples. DOC is found to preferentially bind with Mg than Ca, leading to more likely precipitation of Calcite than dolomite from landfill leachate. The NICA-Donnan model gives a reasonable estimation of dolomite saturation index in a wide range of DOC. Modeling confirms the major precipitation mechanism in terms of alkaline earth metal carbonate. Uncertainties in model parameters are discussed with particular focus on DOC composition, functional group types and density concentration and the influential factors.

  3. Global effects of agriculture on fluvial dissolved organic matter.

    PubMed

    Graeber, Daniel; Boëchat, Iola G; Encina-Montoya, Francisco; Esse, Carlos; Gelbrecht, Jörg; Goyenola, Guillermo; Gücker, Björn; Heinz, Marlen; Kronvang, Brian; Meerhoff, Mariana; Nimptsch, Jorge; Pusch, Martin T; Silva, Ricky C S; von Schiller, Daniel; Zwirnmann, Elke

    2015-11-06

    Agricultural land covers approximately 40% of Earth's land surface and affects hydromorphological, biogeochemical and ecological characteristics of fluvial networks. In the northern temperate region, agriculture also strongly affects the amount and molecular composition of dissolved organic matter (DOM), which constitutes the main vector of carbon transport from soils to fluvial networks and to the sea, and is involved in a large variety of biogeochemical processes. Here, we provide first evidence about the wider occurrence of agricultural impacts on the concentration and composition of fluvial DOM across climate zones of the northern and southern hemispheres. Both extensive and intensive farming altered fluvial DOM towards a more microbial and less plant-derived composition. Moreover, intensive farming significantly increased dissolved organic nitrogen (DON) concentrations. The DOM composition change and DON concentration increase differed among climate zones and could be related to the intensity of current and historical nitrogen fertilizer use. As a result of agriculture intensification, increased DON concentrations and a more microbial-like DOM composition likely will enhance the reactivity of catchment DOM emissions, thereby fuelling the biogeochemical processing in fluvial networks, and resulting in higher ecosystem productivity and CO2 outgassing.

  4. Mineral surface-organic matter interactions: basics and applications

    NASA Astrophysics Data System (ADS)

    Valdrè, G.; Moro, D.; Ulian, G.

    2012-03-01

    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.

  5. Effects of agricultural practices on organic matter degradation in ditches

    PubMed Central

    Hunting, Ellard R.; Vonk, J. Arie; Musters, C.J.M.; Kraak, Michiel H.S.; Vijver, Martina G.

    2016-01-01

    Agricultural practices can result in differences in organic matter (OM) and agricultural chemical inputs in adjacent ditches, but its indirect effects on OM composition and its inherent consequences for ecosystem functioning remain uncertain. This study determined the effect of agricultural practices (dairy farm grasslands and hyacinth bulb fields) on OM degradation by microorganisms and invertebrates with a consumption and food preference experiment in the field and in the laboratory using natural OM collected from the field. Freshly cut grass and hyacinths were also offered to control for OM composition and large- and small mesh-sizes were used to distinguish microbial decomposition and invertebrate consumption. Results show that OM decomposition by microorganisms and consumption by invertebrates was similar throughout the study area, but that OM collected from ditches adjacent grasslands and freshly cut grass and hyacinths were preferred over OM collected from ditches adjacent to a hyacinth bulb field. In the case of OM collected from ditches adjacent hyacinth bulb fields, both microbial decomposition and invertebrate consumption were strongly retarded, likely resulting from sorption and accumulation of pesticides. This outcome illustrates that differences in agricultural practices can, in addition to direct detrimental effects on aquatic organisms, indirectly alter the functioning of adjacent aquatic ecosystems. PMID:26892243

  6. Role of dissolved organic matter in ice photochemistry.

    PubMed

    Grannas, Amanda M; Pagano, Lisa P; Pierce, Brittany C; Bobby, Rachel; Fede, Alexis

    2014-09-16

    In this study, we provide evidence that dissolved organic matter (DOM) plays an important role in indirect photolysis processes in ice, producing reactive oxygen species (ROS) and leading to the efficient photodegradation of a probe hydrophobic organic pollutant, aldrin. Rates of DOM-mediated aldrin loss are between 2 and 56 times faster in ice than in liquid water (depending on DOM source and concentration), likely due to a freeze-concentration effect that occurs when the water freezes, providing a mechanism to concentrate reactive components into smaller, liquid-like regions within or on the ice. Rates of DOM-mediated aldrin loss are also temperature dependent, with higher rates of loss as temperature decreases. This also illustrates the importance of the freeze-concentration effect in altering reaction kinetics for processes occurring in environmental ices. All DOM source types studied were able to mediate aldrin loss, including commercially available fulvic and humic acids and an authentic Arctic snow DOM sample isolated by solid phase extraction, indicating the ubiquity of DOM in indirect photochemistry in environmental ices. PMID:25157605

  7. Effects of agricultural practices on organic matter degradation in ditches.

    PubMed

    Hunting, Ellard R; Vonk, J Arie; Musters, C J M; Kraak, Michiel H S; Vijver, Martina G

    2016-01-01

    Agricultural practices can result in differences in organic matter (OM) and agricultural chemical inputs in adjacent ditches, but its indirect effects on OM composition and its inherent consequences for ecosystem functioning remain uncertain. This study determined the effect of agricultural practices (dairy farm grasslands and hyacinth bulb fields) on OM degradation by microorganisms and invertebrates with a consumption and food preference experiment in the field and in the laboratory using natural OM collected from the field. Freshly cut grass and hyacinths were also offered to control for OM composition and large- and small mesh-sizes were used to distinguish microbial decomposition and invertebrate consumption. Results show that OM decomposition by microorganisms and consumption by invertebrates was similar throughout the study area, but that OM collected from ditches adjacent grasslands and freshly cut grass and hyacinths were preferred over OM collected from ditches adjacent to a hyacinth bulb field. In the case of OM collected from ditches adjacent hyacinth bulb fields, both microbial decomposition and invertebrate consumption were strongly retarded, likely resulting from sorption and accumulation of pesticides. This outcome illustrates that differences in agricultural practices can, in addition to direct detrimental effects on aquatic organisms, indirectly alter the functioning of adjacent aquatic ecosystems. PMID:26892243

  8. Role of dissolved organic matter in ice photochemistry.

    PubMed

    Grannas, Amanda M; Pagano, Lisa P; Pierce, Brittany C; Bobby, Rachel; Fede, Alexis

    2014-09-16

    In this study, we provide evidence that dissolved organic matter (DOM) plays an important role in indirect photolysis processes in ice, producing reactive oxygen species (ROS) and leading to the efficient photodegradation of a probe hydrophobic organic pollutant, aldrin. Rates of DOM-mediated aldrin loss are between 2 and 56 times faster in ice than in liquid water (depending on DOM source and concentration), likely due to a freeze-concentration effect that occurs when the water freezes, providing a mechanism to concentrate reactive components into smaller, liquid-like regions within or on the ice. Rates of DOM-mediated aldrin loss are also temperature dependent, with higher rates of loss as temperature decreases. This also illustrates the importance of the freeze-concentration effect in altering reaction kinetics for processes occurring in environmental ices. All DOM source types studied were able to mediate aldrin loss, including commercially available fulvic and humic acids and an authentic Arctic snow DOM sample isolated by solid phase extraction, indicating the ubiquity of DOM in indirect photochemistry in environmental ices.

  9. Global effects of agriculture on fluvial dissolved organic matter

    PubMed Central

    Graeber, Daniel; Boëchat, Iola G.; Encina-Montoya, Francisco; Esse, Carlos; Gelbrecht, Jörg; Goyenola, Guillermo; Gücker, Björn; Heinz, Marlen; Kronvang, Brian; Meerhoff, Mariana; Nimptsch, Jorge; Pusch, Martin T.; Silva, Ricky C. S.; von Schiller, Daniel; Zwirnmann, Elke

    2015-01-01

    Agricultural land covers approximately 40% of Earth’s land surface and affects hydromorphological, biogeochemical and ecological characteristics of fluvial networks. In the northern temperate region, agriculture also strongly affects the amount and molecular composition of dissolved organic matter (DOM), which constitutes the main vector of carbon transport from soils to fluvial networks and to the sea, and is involved in a large variety of biogeochemical processes. Here, we provide first evidence about the wider occurrence of agricultural impacts on the concentration and composition of fluvial DOM across climate zones of the northern and southern hemispheres. Both extensive and intensive farming altered fluvial DOM towards a more microbial and less plant-derived composition. Moreover, intensive farming significantly increased dissolved organic nitrogen (DON) concentrations. The DOM composition change and DON concentration increase differed among climate zones and could be related to the intensity of current and historical nitrogen fertilizer use. As a result of agriculture intensification, increased DON concentrations and a more microbial-like DOM composition likely will enhance the reactivity of catchment DOM emissions, thereby fuelling the biogeochemical processing in fluvial networks, and resulting in higher ecosystem productivity and CO2 outgassing. PMID:26541809

  10. Organic matter in the ancient Alpine Tethyan Ocean Continental Transition

    NASA Astrophysics Data System (ADS)

    Mateeva, Tsvetomila; Wolff, George; Kusznir, Nick; Wheeler, John; Manataschal, Gianreto

    2016-04-01

    Studies of hydrothermal vents in modern ocean settings suggest that methane produced by serpentinization can support methanotrophic bio-systems. Are such bio-systems locally restricted to hydrothermal vents or are more pervasive, being linked with the geology of serpentinized mantle in the subsurface? Answering this question has implications for our understanding of the global importance of hidden sub-surface bio-systems, the fate of methane and the carbon cycle. The ocean-continent transition (OCT) of magma-poor rifted continental margins, exhumed within mountain belts by continent collision, provides an opportunity to investigate this question. Initial data from the Totalp unit in the Eastern Swiss Alps, representing exhumed OCT of the Alpine Tethyan rifted continental margin, shows the presence of various hydrocarbons (Mateeva et al., in prep.). Samples from other Tethyan OCT locations, consisting of the Tasna nappe and Platta unit of the Eastern Swiss Alps and Chenaillet in the Western Alps, have also been analysed to investigate the presence or absence of methanotrophic biosystems within serpentinized exhumed mantle and associated ophicalcite and syn-rift sediments. Samples from these remnant Tethyan OCT locations are characterized by low and varied organic carbon concentrations that reflect the large lithological diversity of this area. The samples contain hydrocarbons in the form of n-alkanes mostly in the range C20 - C32, polynuclear aromatic hydrocarbons (PAHs) and various biomarkers (e.g. steranes, hopanes). A typical sample from the hydrothermal system in Platta shows the lithological characteristics of a black smoker, but with no indication of a more developed biosystem. Preliminary results from the examined Tethyan OCT locations (Tasna, Platta, Chenaillet) show evidence for the preservation of marine organic matter in the serpentinized mantle and overlying sediments, although there is no unequivocal indication that the organic matter is generated from

  11. Do Long-Term Changes in Organic Matter Inputs to Forest Soils Affect Dissolved Organic Matter Chemistry and Export?

    NASA Astrophysics Data System (ADS)

    Lajtha, K.; Strid, A.; Lee, B. S.

    2014-12-01

    Dissolved organic matter (DOM) production and transport play an important role in regulating organic matter (OM) distribution through a soil profile and ultimately, OM stabilization or export to aquatic systems. The contributions of varying OM inputs to the quality and amount of DOM as it passes through a soil profile remain relatively unknown. The Detrital Input and Removal Treatment (DIRT) site at the H. J. Andrews Experimental Forest in Oregon has undergone 17 years of litter, wood and root input manipulations and allows us to guage shifts in DOM chemistry induced by long-term changes to aboveground and belowground OM additions and exclusions. Using fluorescence and UV spectroscopy to characterize fluorescent properties, extent of decomposition, and sources of DOM in streams and soil solutions collected with lysimeters and soil extractions, we have assessed the importance of fresh OM inputs to DOM chemistry. Soil extracts from DIRT plots had a higher fluorescence index (FI) than lysimeter solutions or stream water. A high FI in surface water is generally interpreted as indicative of a high proportion of microbially-derived DOM. However, we suspect that the high FI in soil extracts is due to a higher proportion of non-aromatic DOM from fresh soil that microorganisms consume in transit through the soil profile to lysimeters or to streams. High redox index (RI) values were observed in lysimeters from the April 2014 sampling compared with the November 2013 sampling. These RI values show evidence of more reducing conditions at the end of the rainy season in the spring compared to the onset of the rainy season in the fall. Lysimeter water collected in No Input, No Litter, and No Root treatments contained high proportions of protein, suggesting the absence of carbon inputs changes activities of the microbial community. Observed variations reflect the viability of using fluorescent properties to explore the terrestrial-aquatic interface.

  12. Fluctuations of dissolved organic matter in river used for drinking water and impacts on conventional treatment plant performance.

    PubMed

    Volk, Christian; Kaplan, Louis A; Robinson, Jeff; Johnson, Bruce; Wood, Larry; Zhu, Hai Wei; LeChevallier, Mark

    2005-06-01

    Natural organic matter (NOM) in drinking water supplies can provide precursors for disinfectant byproducts, molecules that impact taste and odors, compounds that influence the efficacy of treatment, and other compounds that are a source of energy and carbon for the regrowth of microorganisms during distribution. NOM, measured as dissolved organic carbon (DOC), was monitored daily in the White River and the Indiana-American water treatment plant over 22 months. Other parameters were either measured daily (UV-absorbance, alkalinity, color, temperature) or continuously (turbidity, pH, and discharge) and used with stepwise linear regressions to predict DOC concentrations. The predictive models were validated with monthly samples of the river water and treatment plant effluent taken over a 2-year period after the daily monitoring had ended. Biodegradable DOC (BDOC) concentrations were measured in the river water and plant effluent twice monthly for 18 months. The BDOC measurements, along with measurements of humic and carbohydrate constituents within the DOC and BDOC pools, revealed that carbohydrates were the organic fraction with the highest percent removal during treatment, followed by BDOC, humic substances, and refractory DOC.

  13. Key soil functional properties affected by soil organic matter - evidence from published literature

    NASA Astrophysics Data System (ADS)

    Murphy, Brian

    2015-07-01

    The effect of varying the amount of soil organic matter on a range of individual soil properties was investigated using a literature search of published information largely from Australia, but also included relevant information from overseas. Based on published pedotransfer functions, soil organic matter was shown to increase plant available water by 2 to 3 mm per 10 cm for each 1% increase in soil organic carbon, with the largest increases being associated with sandy soils. Aggregate stability increased with increasing soil organic carbon, with aggregate stability decreasing rapidly when soil organic carbon fell below 1.2 to 1.5 5%. Soil compactibility, friability and soil erodibility were favourably improved by increasing the levels of soil organic carbon. Nutrient cycling was a major function of soil organic matter. Substantial amounts of N, P and S become available to plants when the soil organic matter is mineralised. Soil organic matter also provides a food source for the microorganisms involved in the nutrient cycling of N, P, S and K. In soils with lower clay contents, and less active clays such as kaolinites, soil organic matter can supply a significant amount of the cation exchange capacity and buffering capacity against acidification. Soil organic matter can have a cation exchange capacity of 172 to 297 cmol(+)/kg. As the cation exchange capacity of soil organic matter varies with pH, the effectiveness of soil organic matter to contribute to cation exchange capacity below pH 5.5 is often minimal. Overall soil organic matter has the potential to affect a range of functional soil properties.

  14. Soil organic matter on citrus plantation in Eastern Spain

    NASA Astrophysics Data System (ADS)

    Cerdà, Artemi; Pereira, Paulo; Novara, Agata; Prosdocimi, Massimo

    2015-04-01

    Citrus plantations in Eastern Spain are the main crop and Valencia region is the largest world exporter. The traditional plantation are located on flood irrigated areas and the new plantation are located on slopes were drip irrigation is the source of the wetting. It has been demonstrate that the citrus plantations contribute to high erosion rates on slopes (Cerdà et al., 2009b) as it is usual on agriculture land (Cerdà et al., 2009a), but when organic farming is present the soil erosion is much lower (Cerdà and Jurgensen, 2008; Cerdà et al., 2009; Cerdà and Jurgensen, 2011). This is a worldwide phenomenon (Wu et al., 2007; Wu et al., 2011; Xu et al., 2010; Xu et al., 2012a; Xu et al., 2012b), which are a key factor of the high erosion rates in rural areas (García Orenes et al., 2009: García Orenes et al., 20010; García Orenes et al., 2012; Haregewyn et al., 2013; Zhao et al., 2013). The key factor of the contrasted response of soils to the rain in citrus is the organic matter cover. This is why the Soil Erosion and Degradation Research Team developed a survey to determine the soil erosion rates on citrus orchards under different managements. A hundred of samples were collected in a citrus plantation on slope under conventional management (Chemical management), one on organic farming, one on traditional flood irrigated organic farming and one on traditional chemical flooding farm. The organic farming soils were treated with 10000 Kg ha-1 of manure yearly. The results show that the mean soil organic matter content was 1.24 %, 3.54%, 5,43% and 2.1% respectively, which show a clear impact of organic farming in the recovery of the soil organic matter. meanwhile the on the slopes and the flood-irrigated soils are Acknowledgements The research projects GL2008-02879/BTE, LEDDRA 243857 and PREVENTING AND REMEDIATING DEGRADATION OF SOILS IN EUROPE THROUGH LAND CARE (RECARE)FP7- ENV-2013- supported this research. References Cerdà, A., Flanagan, D.C., le Bissonnais

  15. The flux of organic matter through a peatland ecosystem - evidence from thermogravimetric analysis

    NASA Astrophysics Data System (ADS)

    Worrall, Fred; Moody, Catherine; Clay, Gareth

    2016-04-01

    Carbon budgets of peatlands are now common and studies have considered nitrogen, oxygen and energy budgets, but no study has considered the whole composition of the organic matter as it transfers through and into a peatland. Organic matter samples were taken from each organic matter reservoir found in and each fluvial flux from a peatland and analysed the samples by thermogravimetric analysis. The samples analysed were: aboveground, belowground, heather, mosses and sedges, litter layer, a peat core, and monthly samples of particulate and dissolved organic matter. All organic matter samples were taken from a 100% peat catchment within Moor House National Nature Reserve in the North Pennines, UK, and collected samples were compared to standards of lignin, cellulose, humic acid and plant protein. Results showed that the thermogravimetric trace of the sampled organic matter were distinctive with the DOM traces being marked out by very low thermal stability relative other organic matter types. The peat profile shows a significant trend with depth from vegetation- to lignin-like composition. When all traces are weighted according to the observed dry matter and carbon budgets for the catchment then it is possible to judge what has been lost in the transition through and into the ecosystem. By plotting this "lost" trace it possible to assess its composition which is either 97% cellulose and 3% humic acid or 92% and 8% lignin. This has important implications for what controls the organic matter balance of peatlands and it suggests that the oxidation state (OR) of peatland is less than 1.

  16. Vehicular emissions of organic particulate matter in Sao Paulo, Brazil

    NASA Astrophysics Data System (ADS)

    Oyama, B. S.; Andrade, M. F.; Herckes, P.; Dusek, U.; Röckmann, T.; Holzinger, R.

    2015-12-01

    Vehicular emissions have a strong impact on air pollution in big cities. Many factors affect these emissions: type of vehicle, type of fuel, cruising velocity, and brake use. This study focused on emissions of organic compounds by Light (LDV) and Heavy (HDV) duty vehicle exhaust. The study was performed in the city of Sao Paulo, Brazil, where vehicles run on different fuels: gasoline with 25 % ethanol (called gasohol), hydrated ethanol, and diesel (with 5 % of biodiesel). The vehicular emissions are an important source of pollutants and the principal contribution to fine particulate matter (smaller than 2.5 μm, PM2.5) in Sao Paulo. The experiments were performed in two tunnels: Janio Quadros (TJQ) where 99 % of the vehicles are LDV, and Rodoanel Mario Covas (TRA) where up to 30 % of the fleet was HDV. The PM2.5 samples were collected on quartz filters in May and July 2011 at TJQ and TRA, respectively, using two samplers operating in parallel. The samples were analyzed by Thermal-Desorption Proton-Transfer-Reaction Mass-Spectrometry (TD-PTR-MS), and by Thermal-Optical Transmittance (TOT). The organic aerosol (OA) desorbed at TD-PTR-MS represented around 30 % of the OA estimated by the TOT method, mainly due to the different desorption temperatures, with a maximum of 870 and 350 °C for TOT and TD-PTR-MS, respectively. Average emission factors (EF) organic aerosol (OA) and organic carbon (OC) were calculated for HDV and LDV fleet. We found that HDV emitted more OA and OC than LDV, and that OC emissions represented 36 and 43 % of total PM2.5 emissions from LDV and HDV, respectively. More than 700 ions were identified by TD-PTR-MS and the EF profiles obtained from HDV and LDV exhibited distinct features. Nitrogen-containing compounds measured in the desorbed material up to 350 °C contributed around 20 % to the EF values for both types of vehicles, possibly associated with incomplete fuel burning. Additionally, 70 % of the organic compounds measured from the aerosol

  17. Chemical composition of dissolved organic matter draining permafrost soils

    NASA Astrophysics Data System (ADS)

    Ward, Collin P.; Cory, Rose M.

    2015-10-01

    Northern circumpolar permafrost soils contain roughly twice the amount of carbon stored in the atmosphere today, but the majority of this soil organic carbon is perennially frozen. Climate warming in the arctic is thawing permafrost soils and mobilizing previously frozen dissolved organic matter (DOM) from deeper soil layers to nearby surface waters. Previous studies have reported that ancient DOM draining deeper layers of permafrost soils was more susceptible to degradation by aquatic bacteria compared to modern DOM draining the shallow active layer of permafrost soils, and have suggested that DOM chemical composition may be an important control for the lability of DOM to bacterial degradation. However, the compositional features that distinguish DOM drained from different depths in permafrost soils are poorly characterized. Thus, the objective of this study was to characterize the chemical composition of DOM drained from different depths in permafrost soils, and relate these compositional differences to its susceptibility to biological degradation. DOM was leached from the shallow organic mat and the deeper permafrost layer of soils within the Imnavait Creek watershed on the North Slope of Alaska. DOM draining both soil layers was characterized in triplicate by coupling ultra-high resolution mass spectrometry, 13C solid-state NMR, and optical spectroscopy methods with multi-variate statistical analyses. Reproducibility of replicate mass spectra was high, and compositional differences resulting from interfering species or isolation effects were significantly smaller than differences between DOM drained from each soil layer. All analyses indicated that DOM leached from the shallower organic mat contained higher molecular weight, more oxidized, and more unsaturated aromatic species compared to DOM leached from the deeper permafrost layer. Bacterial production rates and bacterial efficiencies were significantly higher for permafrost compared to organic mat DOM

  18. Do aggregate stability and soil organic matter content increase following organic inputs?

    NASA Astrophysics Data System (ADS)

    Lehtinen, Taru; Gísladóttir, Guðrún; van Leeuwen, Jeroen P.; Bloem, Jaap; Steffens, Markus; Vala Ragnarsdóttir, Kristin

    2014-05-01

    Agriculture is facing several challenges such as loss of soil organic matter (SOM); thus, sustainable farming management practices are needed. Organic farming is growing as an alternative to conventional farming; in Iceland approximately 1% and in Austria 16% of utilized agricultural area is under organic farming practice. We analyzed the effect of different farming practices (organic, and conventional) on soil physicochemical and microbiological properties in grassland soils in Iceland and cropland soils in Austria. Organic farms differed from conventional farms by absence of chemical fertilizers and pesticide use. At these farms, we investigated soil physicochemical (e.g. soil texture, pH, CAL-extractable P and K) and microbiological properties (fungal and bacterial biomass and activity). The effects of farming practices on soil macroaggregate stability and SOM quantity, quality and distribution between different fractions were studied following a density fractionation. In Iceland, we sampled six grassland sites on Brown (BA) and Histic (HA) Andosols; two sites on extensively managed grasslands, two sites under organic and two sites under conventional farming practice. In Austria, we sampled four cropland sites on Haplic Chernozems; two sites under organic and two sites under conventional farming practice. We found significantly higher macroaggregate stability in the organic compared to the conventional grasslands in Iceland. In contrast, slightly higher macroaggregation in conventional compared to the organic farming practice was found in croplands in Austria, although the difference was not significant. Macroaggregates were positively correlated with fungal biomass in Iceland, and with Feo and fungal activity in Austria. In Austria, SOM content and nutrient status (except for lower CAL-extractable P at one site) were similar between organic and conventional farms. Our results show that the organic inputs may have enhanced macroaggregation in organic farming

  19. Vertical transport of particulate organic matter regulated by fjord topography

    NASA Astrophysics Data System (ADS)

    Erlandsson, Carina P.

    2008-03-01

    The deepwater in many areas with restricted water exchange suffers from low oxygen concentrations due to degradation of organic matter. The objective of this study was to investigate how topography may influence the vertical transport, Fc, of particulate organic matter, POM, to the deepwater. A conceptual/analytical model for Fc was developed covering the combination of the three possible sources of POM/nutrients to an enclosed area; the coastal water, local supply, and nutrient rich local deepwater. The mathematical formulation of the conceptual model includes several factors describing to which degree various physical mechanisms in the fjord are influencing Fc. The model consists of submodels for the different sources of POM/nutrients. A one-dimensional process oriented numerical model was used to test the conceptual model. Restricted water exchange with the coastal water led to decreased import of POM and thereby decreased vertical transport, Fc, of coastal POM. The contribution to Fc by local input of nutrients to the surface layer was described by a function of the residence time of the water above sill level, Tsw and the time Tp it takes for POM produced in the surface layer to settle below sill level. The recirculation of POM produced due to basin water renewals was shown to be a function of several factors: The relation between the depth of photic zone, Hp and the sill depth, Ht, the vertical velocity of the rising nutrient rich water mass versus the settling velocity of POM, etc. The results based on the conceptual submodels agreed well with the results from the process oriented numerical model. Methods to identify the trophic state of coastal waters, and also simple models to calculate the effect of a local point source, can be found in literature. However, using the model developed in this paper the effects of nutrient enrichment from different sources can be quantified in a simple and more efficient way than earlier. The model can thus be used to

  20. Heavy metals fractionation and organic matter mineralisation in contaminated calcareous soil amended with organic materials.

    PubMed

    Clemente, Rafael; Escolar, Angeles; Bernal, M Pilar

    2006-10-01

    Degradation of organic matter (OM) from organic amendments used in the remediation of metal contaminated soils leads to changes in soil chemical properties shortly after their addition, which may affect the soil metal distribution. The effects of two differing organic amendments on OM mineralisation and fractionation of heavy metals in a contaminated soil were investigated in an incubation experiment. The treatments were: control unamended soil, soil amended with fresh cow manure, and soil amended with a compost having a high maturity degree. The soil used was characteristic of the mining area at La Unión (Murcia, Spain) with 28% CaCO(3) and sandy-loam texture (pH 7.7; 2602 mg kg(-1)Zn; 1572 mg kg(-1)Pb). Manure and compost C-mineralisation after 56 days (24% and 3.8%, respectively) were below values reported previously for uncontaminated soils. Both amendments favoured Zn and Pb fixation, particularly the manure. Mn solubility increased at the beginning of the experiment due to a pH effect, and only Cu solubility increased through organic matter chelation in both amended soils.

  1. The Isiokpo oil-pipeline leakage: total organic carbon/organic matter contents of affected soils.

    PubMed

    Osuji, Leo C; Adesiyan, Samuel O

    2005-08-01

    The environmental impact of the 1997 leakage of the high-pressure crude-oil pipeline at Isiokpo in the Niger Delta in the southeast of Nigeria was evaluated, with particular reference to total-organic-carbon (TOC) and total-organic-matter (TOM) contents of soils within the vicinity of the oil spillage. The soils, taken from depths of 0-15 cm (surface) and 15-30 cm (subsurface), were found to be more acidic (pH 4.2-5.6) than the unpolluted soils, with a high average moisture content of 6.8%. The extractable hydrocarbon content ranged from 2.71-3.48 mg/kg, indicating hydrocarbon contamination. However, contrary to expectation, the TOC and TOM contents of the polluted soils did not show any significant increase in concentration, supposedly due to natural rehabilitation of the affected mat layer of soils. Thus, notwithstanding the possible proliferation of heterotrophic organisms by the presence of the added petroleum hydrocarbons, environmental conditions such as weathering and climatic predispositions, as well as physico-chemical parameters such as pH, moisture content, and temperature must have encumbered the carbon-mineralizing capacity of the heterotrophs, thereby reducing the turnover of carbon and the decomposition of organic matter. The restrictions by high moisture content might not come directly from H(2)O itself, but are probably a consequence of hindered soil ventilation, which reduces O(2) supply and gaseous diffusion, conditions that might have been substantially aggravated by the added petroleum hydrocarbons.

  2. Electron Shuttling Capacity of Solid-Phase Organic Matter in Forest Soils

    NASA Astrophysics Data System (ADS)

    Patel, A.; Zhao, Q.; Yang, Y.

    2015-12-01

    Soil organic matter, as an electron shuttle, plays an important role in regulating the biogeochemical cycles of metals, especially the redox reactions for iron. Microorganisms can reduce soil organic matter under anaerobic conditions, and biotically-reduced soil organic matter can abiotically donate electrons to ferric oxides. Such soil organic matter-mediated electron transport can facilitate the interactions between microorganisms and insoluble terminal electron acceptors, i.e. iron minerals. Most previous studies have been focused on the electron shuttling processes through dissolved soil organic matter, and scant information is available for solid-phase soil organic matter. In this study, we aim to quantify the electron accepting capacity for solid-phase organic matter in soils collected from four different forests in the United States, including Truckee (CA), Little Valley (NV), Howland (ME) and Hart (MI). We used Shewanella oneidensisMR-1 to biotically reduce soil slurries, and then quantified the electrons transferred to solid-phase and solution-phase organic matter by reacting them with Fe(III)-nitrilotriacetic acid (Fe(III)-NTA). The generation of Fe(II) was measured by a ferrozine assay to calculate the electron accepting capacity of soil organic matter. Our preliminary results showed that the Truckee soil organic matter can accept 0.51±0.07 mM e-/mol carbon. We will measure the electron accepting capacity for four different soils and correlate them to the physicochemical properties of soils. Potential results will provide information about the electron accepting capacity of solid-phase soil organic matter and its governing factors, with broad implication on the coupled biogeochemical cycles of carbon and iron.

  3. Effects of Natural Organic Matter on Stability, Transport and Deposition of Engineered Nano-particles in Porous Media

    EPA Science Inventory

    The interaction of nano-particles and organic substances, like natural organic matter, could have significant influence on the fate, transport and bioavailability of toxic substances. Natural organic matter (NOM) is a mixture of chemically complex polyelectrolytes with varying m...

  4. Enhancement of the natural organic matter removal from drinking water by nanofiltration.

    PubMed

    Matilainen, A; Liikanen, R; Nyström, M; Lindqvist, N; Tuhkanen, T

    2004-03-01

    Finnish surface waters are abundant in natural organic matter. Natural organic matter can be removed from drinking water in a water treatment process by coagulation and filtration. The standard treatment operations are not able to remove the smallest molar mass fraction of organic matter and the intermediate molar mass matter is only partly removed. The removal of residual natural organic matter from drinking water by nanofiltration was evalueted in this study. Three different nanofiltration membranes were compared in filtering six pre-treated surface waters. The total organic carbon content of the feed waters varied from 2.0 to 4.2 mg l(-1). Other water quality parameters measured were conductivity, alkalinity, hardness, UV-absorbance, SUVA, E2/E3 value and molecular size distribution by high-performance size-exclusion chromatography. The natural organic matter removal efficiencies of the membranes were good and varied between 100% and 49%, and between 85% and 47% according to molecular size distribution and total organic carbon measurements, respectively. Removal of different molecular size fractions varied from 100% to 56%, 100% to 54% and 88% to 19%, regarding high molar mass, intermediate molar mass and low molar mass organic matter, respectively. The Desal-5 DL membrane produced the highest natural organic matter removals.

  5. Influence of soil organic matter composition on the partition of organic compounds

    USGS Publications Warehouse

    Rutherford, D.W.; Chiou, C.T.; Klle, D.E.

    1992-01-01

    The sorption at room temperature of benzene and carbon tetrachloride from water on three high-organic-content soils (muck, peat, and extracted peat) and on cellulose was determined in order to evaluate the effect of sorbent polarity on the solute partition coefficients. The isotherms are highly linear for both solutes on all the organic matter samples, which is consistent with a partition model. For both solutes, the extracted peat shows the greatest sorption capacity while the cellulose shows the lowest capacity; the difference correlates with the polar-to-nonpolar group ratio [(O + N)/C] of the sorbent samples. The relative increase of solute partition coefficient (Kom) with a decrease of sample polar content is similar for both solutes, and the limiting sorption capacity on a given organic matter sample is comparable between the solutes. This observation suggests that one can estimate the polarity effect of a sample of soil organic matter (SOM) on Kom of various nonpolar solutes by determining the partition coefficient of single nonpolar solute when compositional analysis of the SOM is not available. The observed dependence of Kom on sample polarity is used to account for the variation of Kom values of individual compounds on different soils that results from change in the polar group content of SOM. On the assumption that the carbon content of SOM in "ordinary soils" is 53-63%, the calculated variation of Kom is a factor of ???3. This value is in agreement with the limit of variation of most Kom data with soils of relatively high SOM contents.

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

    PubMed

    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.

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

    PubMed

    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. PMID:24972176

  8. Sorptive stabilization of organic matter by amorphous Al hydroxide

    NASA Astrophysics Data System (ADS)

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

    2010-03-01

    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 beech forest. The stabilization of OM by sorption was analyzed by comparing the CO 2 mineralized during the incubation of sorbed and non-sorbed OM. The mineralization of OM was evaluated based in terms of (i) the availability of the am-Al(OH) 3, thus surface OM loadings, (ii) spectral properties of OM, and (iii) the presence of phosphate as a competitor for OM. This was done by varying the solid-to-solution ratio (SSR = 0.02-1.2 g L -1) during sorption. At low SSRs, hence limited am-Al(OH) 3 availability, only small portions of dissolved OM were sorbed; for OM from Oa horizons, the mineralization of the sorbed fraction exceeded that of the original dissolved OM. The likely reason is competition with phosphate for sorption sites favouring the formation of weak mineral-organic bindings and the surface accumulation of N-rich, less aromatic and less complex OM. This small fraction controlled the mineralization of sorbed OM even at higher SSRs. At higher SSRs, i.e., with am-Al(OH) 3 more available, competition of phosphate decreased and aromatic compounds were sorbed selectively, which resulted in pronounced resistance of sorbed OM against decay. The combined OC mineralization of sorbed and non-sorbed OM was 12-65% less than that of the original DOM. Sorbed OM contributed only little to the overall OC mineralization. Stabilization of OC increased in direct proportion to am-Al(OH) 3 availability, despite constant aromatic C (˜30%). The strong stabilization at higher mineral availability is primarily governed by strong Al-OM bonds formed under less competitive conditions. Due to these strong bonds and the resulting strong stabilization, the surface loading, a proxy for the

  9. Sustaining effect of soil warming on organic matter decomposition

    NASA Astrophysics Data System (ADS)

    Hou, Ruixing; Ouyang, Zhu; Dorodnikov, Maxim; Wilson, Glenn; Kuzyakov, Yakov

    2015-04-01

    Global warming affects various parts of carbon (C) cycle including acceleration of soil organic matter (SOM) decomposition with strong feedback to atmospheric CO2 concentration. Despite many soil warming studies showed changes of microbial community structure, only very few were focused on sustainability of soil warming on microbial activity associated with SOM decomposition. Two alternative hypotheses: 1) acclimation because of substrate exhaustion and 2) sustaining increase of microbial activity with accelerated decomposition of recalcitrant SOM pools were never proven under long term field conditions. This is especially important in the nowadays introduced no-till crop systems leading to redistribution of organic C at the soil surface, which is much susceptible to warming effects than the rest of the profile. We incubated soil samples from a four-year warming experiment with tillage (T) and no-tillage (NT) practices under three temperatures: 15, 21, and 27 °C, and related the evolved total CO2 efflux to changes of organic C pools. Warmed soils released significantly more CO2 than the control treatment (no warming) at each incubation temperature, and the largest differences were observed under 15 °C (26% increase). The difference in CO2 efflux from NT to T increase with temperature showing high vulnerability of C stored in NT to soil warming. The Q10 value reflecting the sensitivity of SOM decomposition to warming was lower for warmed than non-warmed soil indicating better acclimation of microbes or lower C availability during long term warming. The activity of three extracellular enzymes: β-glucosidase, chitinase, sulphatase, reflecting the response of C, N and S cycles to warming, were significantly higher under warming and especially under NT compared to two other respective treatments. The CO2 released during 2 months of incubation consisted of 85% from recalcitrant SOM and the remaining 15% from microbial biomass and extractable organic C based on the

  10. Macroinvertebrate and organic matter export from headwater tributaries of a Central Appalachian stream

    EPA Science Inventory

    Headwater streams export organisms and other materials to their receiving streams and macroinvertebrate drift can shape colonization dynamics in downstream reaches while providing food for downstream consumers. Spring-time macroinvertebrate drift and organic matter export was me...

  11. Sources and Distribution of Organic Matter in Sediments of the Louisiana Continental Shelf

    EPA Science Inventory

    Both riverine and marine sources of organic matter (OM) contribute to sediment organic pools, and either source can contribute significantly to sediment accumulation, burial, and remineralization rates on river dominated continental shelf systems. For the Louisiana continental sh...

  12. Tillage, crop rotation, and organic amendment effect on changes in soil organic matter.

    PubMed

    Rickman, R; Douglas, C; Albrecht, S; Berc, J

    2002-01-01

    Carbon sequestration in agricultural soils is controlled by the balance of added organic residues and microbial oxidation of both residues and native organic matter (OM) as moderated by management and tillage. The PC-based model CQESTR predicts decomposition of residues, organic amendments and soil OM, based on cropping practices. CQESTR uses RUSLE (Revised Universal Soil Loss Equation) crop rotation and management practice, crop production, and operation databases. These data are supplemented with residue nitrogen and soil OM, bulk density, and layer thickness. CQESTR was calibrated with soil carbon data from 70-year-long experiments at the Research Center at Pendleton, OR. The calibrated model provides estimates with a 95% confidence interval of 0.33% OM. Validation at 11 independent sites resulted in a matching of observed with calculated OM with a 95% confidence interval of 0.55% OM. A 12th site, with a history of severe erosion, provided a poor match.

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

    PubMed

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

    2016-07-01

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

  14. Photodegradation of dissolved organic matter in ice under solar irradiation.

    PubMed

    Xue, Shuang; Wang, Chao; Zhang, Zhaohong; Song, Youtao; Liu, Qiang

    2016-02-01

    The photodegradation behavior of dissolved organic matter (DOM) with different origins in ice under solar irradiation was investigated. Exposure to sunlight at 2.7 × 10(5) J m(-2) resulted in dissolved organic carbon (DOC) reductions of 22.1-36.5% in ice. The naturally occurring DOM had higher photodegradation potentials than the wastewater-derived DOM in ice. Ultraviolet (UV)-absorbing compounds in DOM, regardless of DOM origin, had much higher photodegradation potentials than gross DOC in ice. The susceptibility of UV-absorbing compounds with natural origin to sunlight exposure in ice was higher than those derived from wastewater. Trihalomethane (THM) precursors were more susceptible to photochemical reactions than gross DOC and haloacetic acid (HAA) precursors in ice. THM precursors in naturally occurring DOM were more photoreactive than those in wastewater-derived DOM in ice, while the photoreactivity of HAA precursors in ice was independent of DOM origin. In ice, the photoreactivity of humic-like fluorescent materials, regardless of DOM origin, was higher than that of gross DOC and protein-like fluorescent materials. DOC reductions caused by sunlight irradiation were found to be negatively correlated to DOC levels, and positively correlated to the aromaticity of DOM. The photodegradation of both wastewater-derived and naturally occurring DOM in ice was significantly facilitated at both acid and alkaline pH, as compared to neutral pH. The photodegradation of DOM in ice, regardless of the origin, was facilitated by nitrate ion [Formula: see text] , nitrite ion [Formula: see text] , ferric ion (Fe(3+)) and ferrous ion (Fe(2+)), and on the other hand, was inhibited by chloridion ion (Cl(-)) and copper ion (Cu(2+)).

  15. Natural organic matter fouling behaviors on superwetting nanofiltration membranes.

    PubMed

    Shan, Linglong; Fan, Hongwei; Guo, Hongxia; Ji, Shulan; Zhang, Guojun

    2016-04-15

    Nanofiltration has been widely recognized as a promising technology for the removal of micro-molecular organic components from natural water. Natural organic matter (NOM), a very important precursor of disinfection by-products, is currently considered as the major cause of membrane fouling. It is necessary to develop a membrane with both high NOM rejection and anti-NOM fouling properties. In this study, both superhydrophilic and superhydrophobic nanofiltration membranes for NOM removal have been fabricated. The fouling behavior of NOM on superwetting nanofiltration membranes has been extensively investigated by using humic acid (HA) as the model foulant. The extended Derjaguin-Landau-Verwey-Overbeek approach and nanoindentor scratch tests suggested that the superhydrophilic membrane had the strongest repulsion force to HA due to the highest positive total interaction energy (ΔG(TOT)) value and the lowest critical load. Excitation emission matrix analyses of natural water also indicated that the superhydrophilic membrane showed resistance to fouling by hydrophobic substances and therefore high removal thereof. Conversely, the superhydrophobic membrane showed resistance to fouling by hydrophilic substances and therefore high removal capacity. Long-term operation suggested that the superhydrophilic membrane had high stability due to its anti-NOM fouling capacity. Based on the different anti-fouling properties of the studied superwetting membranes, a combination of superhydrophilic and superhydrophobic membranes was examined to further improve the removal of both hydrophobic and hydrophilic pollutants. With a combination of superhydrophilic and superhydrophobic membranes, the NOM rejection (RUV254) and DOC removal rates (RDOC) could be increased to 83.6% and 73.3%, respectively. PMID:26900973

  16. Chemodiversity of dissolved organic matter in the Amazon Basin

    NASA Astrophysics Data System (ADS)

    Gonsior, Michael; Valle, Juliana; Schmitt-Kopplin, Philippe; Hertkorn, Norbert; Bastviken, David; Luek, Jenna; Harir, Mourad; Bastos, Wanderley; Enrich-Prast, Alex

    2016-07-01

    Regions in the Amazon Basin have been associated with specific biogeochemical processes, but a detailed chemical classification of the abundant and ubiquitous dissolved organic matter (DOM), beyond specific indicator compounds and bulk measurements, has not yet been established. We sampled water from different locations in the Negro, Madeira/Jamari and Tapajós River areas to characterize the molecular DOM composition and distribution. Ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) combined with excitation emission matrix (EEM) fluorescence spectroscopy and parallel factor analysis (PARAFAC) revealed a large proportion of ubiquitous DOM but also unique area-specific molecular signatures. Unique to the DOM of the Rio Negro area was the large abundance of high molecular weight, diverse hydrogen-deficient and highly oxidized molecular ions deviating from known lignin or tannin compositions, indicating substantial oxidative processing of these ultimately plant-derived polyphenols indicative of these black waters. In contrast, unique signatures in the Madeira/Jamari area were defined by presumably labile sulfur- and nitrogen-containing molecules in this white water river system. Waters from the Tapajós main stem did not show any substantial unique molecular signatures relative to those present in the Rio Madeira and Rio Negro, which implied a lower organic molecular complexity in this clear water tributary, even after mixing with the main stem of the Amazon River. Beside ubiquitous DOM at average H / C and O / C elemental ratios, a distinct and significant unique DOM pool prevailed in the black, white and clear water areas that were also highly correlated with EEM-PARAFAC components and define the frameworks for primary production and other aspects of aquatic life.

  17. Chemotaxis toward phytoplankton drives organic matter partitioning among marine bacteria

    PubMed Central

    Smriga, Steven; Fernandez, Vicente I.; Mitchell, James G.; Stocker, Roman

    2016-01-01

    The microenvironment surrounding individual phytoplankton cells is often rich in dissolved organic matter (DOM), which can attract bacteria by chemotaxis. These “phycospheres” may be prominent sources of resource heterogeneity in the ocean, affecting the growth of bacterial populations and the fate of DOM. However, these effects remain poorly quantified due to a lack of quantitative ecological frameworks. Here, we used video microscopy to dissect with unprecedented resolution the chemotactic accumulation of marine bacteria around individual Chaetoceros affinis diatoms undergoing lysis. The observed spatiotemporal distribution of bacteria was used in a resource utilization model to map the conditions under which competition between different bacterial groups favors chemotaxis. The model predicts that chemotactic, copiotrophic populations outcompete nonmotile, oligotrophic populations during diatom blooms and bloom collapse conditions, resulting in an increase in the ratio of motile to nonmotile cells and in the succession of populations. Partitioning of DOM between the two populations is strongly dependent on the overall concentration of bacteria and the diffusivity of different DOM substances, and within each population, the growth benefit from phycospheres is experienced by only a small fraction of cells. By informing a DOM utilization model with highly resolved behavioral data, the hybrid approach used here represents a new path toward the elusive goal of predicting the consequences of microscale interactions in the ocean. PMID:26802122

  18. Results of the 2008 dissolved organic matter fluorescence intercalibration study

    NASA Astrophysics Data System (ADS)

    Murphy, K. R.; Butler, K.; Spencer, R. G.; Boehme, J.; Aiken, G.

    2009-12-01

    In 2008, 20 laboratories around the world participated in an intercalibration study of organic matter fluorescence measurements via Excitation-Emission Matrix Spectroscopy (EEMS). The goal was to assess the variability of fluorescence measurements obtained for identical samples (n = 5 natural samples, Suwanee River Fulvic Acid, quinine sulphate and four Starna Fluorescence Reference cells) by different laboratories, and to examine potential sources of this variability. Operator error was found to be a significant source of variability, with 6 laboratories submitting erroneous EEMs in an initial round. Uncorrected EEMs were significantly different from corrected EEMs, particularly at relatively low and relatively high excitation (λex) and emission (λem) wavelengths. When data from each lab were corrected according to a standard set of algorithms, the variability between EEMs for the same sample measured by different labs was wavelength dependent, with EEMs normalized to raman areas more similar at low λex and λem, and EEMs normalized to quinine sulphate equivalents more similar at higher wavelengths. The results confirm the importance of (1) applying spectral corrections prior to comparing fluorescence data acquired on different instruments, (2) full reporting of correction procedures and implementation according to an agreed standard protocol, and (3) strict implementation of quality assurance protocols prior to reporting EEMs.

  19. Soil microstructure and organic matter: keys for chlordecone sequestration.

    PubMed

    Woignier, T; Fernandes, P; Soler, A; Clostre, F; Carles, C; Rangon, L; Lesueur-Jannoyer, M

    2013-11-15

    Past applications of chlordecone, a persistent organochlorine pesticide, have resulted in diffuse pollution of agricultural soils, and these have become sources of contamination of cultivated crops as well as terrestrial and marine ecosystems. Chlordecone is a very stable and recalcitrant molecule, mainly present in the solid phase, and has a strong affinity for organic matter. To prevent consumer and ecosystem exposure, factors that influence chlordecone migration in the environment need to be evaluated. In this study, we measured the impact of incorporating compost on chlordecone sequestration in andosols as a possible way to reduce plant contamination. We first characterized the transfer of chlordecone from soil to plants (radish, cucumber, and lettuce). Two months after incorporation of the compost, soil-plant transfers were reduced by a factor of 1.9-15 depending on the crop. Our results showed that adding compost modified the fractal microstructure of allophane clays thus favoring chlordecone retention in andosols. The complex structure of allophane and the associated low accessibility are important characteristics governing the fate of chlordecone. These results support our proposal for an alternative strategy that is quite the opposite of total soil decontamination: chlordecone sequestration.

  20. [Effects of dissolved organic matter on copper absorption by ryegrass].

    PubMed

    Tang, Chao; Wang, Bin; Liu, Man-Qiang; Hu, Feng; Li, Hui-Xin; Jiao, Jia-Guo

    2012-08-01

    In this study, dissolved organic matter (DOM) was extracted from earthworm casts and from the cattle manure with which the earthworms were fed, and a water culture experiment was conducted to study the effects of the DOM on the copper (Cu2+) absorption by ryegrass in the presence of different concentration Cu2+ (0, 5 and 10 mg x L(-1)). With the increasing concentration of Cu2+ in the medium, there was a gradual decrease in the dry mass of ryegrass shoots and roots and in the root length, surface area, volume, and tip number. In the presence of medium Cu2+, DOM increased the biomass of shoots and roots and the root length, surface area, volume, and tip number significantly. DOM reduced the Cu2+ concentration in roots, promoted the Cu2+ translocation from roots to shoots, and significantly increased the Cu2+ accumulation in shoots. The DOM from earthworm casts had better effects than that from cattle manure, and high concentration DOM had better effects than low concentration DOM. PMID:23189712

  1. Soil microstructure and organic matter: keys for chlordecone sequestration.

    PubMed

    Woignier, T; Fernandes, P; Soler, A; Clostre, F; Carles, C; Rangon, L; Lesueur-Jannoyer, M

    2013-11-15

    Past applications of chlordecone, a persistent organochlorine pesticide, have resulted in diffuse pollution of agricultural soils, and these have become sources of contamination of cultivated crops as well as terrestrial and marine ecosystems. Chlordecone is a very stable and recalcitrant molecule, mainly present in the solid phase, and has a strong affinity for organic matter. To prevent consumer and ecosystem exposure, factors that influence chlordecone migration in the environment need to be evaluated. In this study, we measured the impact of incorporating compost on chlordecone sequestration in andosols as a possible way to reduce plant contamination. We first characterized the transfer of chlordecone from soil to plants (radish, cucumber, and lettuce). Two months after incorporation of the compost, soil-plant transfers were reduced by a factor of 1.9-15 depending on the crop. Our results showed that adding compost modified the fractal microstructure of allophane clays thus favoring chlordecone retention in andosols. The complex structure of allophane and the associated low accessibility are important characteristics governing the fate of chlordecone. These results support our proposal for an alternative strategy that is quite the opposite of total soil decontamination: chlordecone sequestration. PMID:24056248

  2. The Organic Matter Biogeochemistry of the Congo River

    NASA Astrophysics Data System (ADS)

    Spencer, R. G.; Hernes, P.; Wabakanghanzi, J.; Bienvenu, D. J.; Six, J.

    2015-12-01

    Organic matter (OM) represents a fundamental link between terrestrial and aquatic carbon cycles and plays an essential role in aquatic ecosystem biogeochemistry. The Congo River, which drains pristine tropical forest and savannah is the second largest exporter of terrestrial carbon to the ocean, and represents a historically understudied basin. Our ongoing projects in the Congo Basin aim to provide pertinent information on transport and emissions of carbon by rivers that need to be incorporated into carbon budgets of terrestrial ecosystems. To date the Congo Basin has seen only limited perturbation but the carbon locked away in the Congo, as in other tropical rainforests is increasingly vulnerable to release into the aquatic system and the atmosphere. However, riverine carbon transport (both of OM to the oceans and release of CO2 to the atmosphere) as a driver of global carbon cycling is still largely overlooked. Here we present data from a multi-season field campaign to quantify the transport fluxes, mineralization fluxes, and chemical character of Congo River OM, and to elucidate how these properties relate to each other and vary seasonally driven by hydrology within the Congo Basin. Existing data demonstrates that although tropical rivers do not experience the seasonal climatic extremes of temperate or northern high-latitude rivers, they all demonstrate similar effects due to changing hydrologic inputs with respect to OM dynamics. Specifically flushing periods appear to warrant further study as maximal export of reactive freshly leached plant material occurs during this time period.

  3. Chemotaxis toward phytoplankton drives organic matter partitioning among marine bacteria.

    PubMed

    Smriga, Steven; Fernandez, Vicente I; Mitchell, James G; Stocker, Roman

    2016-02-01

    The microenvironment surrounding individual phytoplankton cells is often rich in dissolved organic matter (DOM), which can attract bacteria by chemotaxis. These "phycospheres" may be prominent sources of resource heterogeneity in the ocean, affecting the growth of bacterial populations and the fate of DOM. However, these effects remain poorly quantified due to a lack of quantitative ecological frameworks. Here, we used video microscopy to dissect with unprecedented resolution the chemotactic accumulation of marine bacteria around individual Chaetoceros affinis diatoms undergoing lysis. The observed spatiotemporal distribution of bacteria was used in a resource utilization model to map the conditions under which competition between different bacterial groups favors chemotaxis. The model predicts that chemotactic, copiotrophic populations outcompete nonmotile, oligotrophic populations during diatom blooms and bloom collapse conditions, resulting in an increase in the ratio of motile to nonmotile cells and in the succession of populations. Partitioning of DOM between the two populations is strongly dependent on the overall concentration of bacteria and the diffusivity of different DOM substances, and within each population, the growth benefit from phycospheres is experienced by only a small fraction of cells. By informing a DOM utilization model with highly resolved behavioral data, the hybrid approach used here represents a new path toward the elusive goal of predicting the consequences of microscale interactions in the ocean.

  4. Chemotaxis toward phytoplankton drives organic matter partitioning among marine bacteria.

    PubMed

    Smriga, Steven; Fernandez, Vicente I; Mitchell, James G; Stocker, Roman

    2016-02-01

    The microenvironment surrounding individual phytoplankton cells is often rich in dissolved organic matter (DOM), which can attract bacteria by chemotaxis. These "phycospheres" may be prominent sources of resource heterogeneity in the ocean, affecting the growth of bacterial populations and the fate of DOM. However, these effects remain poorly quantified due to a lack of quantitative ecological frameworks. Here, we used video microscopy to dissect with unprecedented resolution the chemotactic accumulation of marine bacteria around individual Chaetoceros affinis diatoms undergoing lysis. The observed spatiotemporal distribution of bacteria was used in a resource utilization model to map the conditions under which competition between different bacterial groups favors chemotaxis. The model predicts that chemotactic, copiotrophic populations outcompete nonmotile, oligotrophic populations during diatom blooms and bloom collapse conditions, resulting in an increase in the ratio of motile to nonmotile cells and in the succession of populations. Partitioning of DOM between the two populations is strongly dependent on the overall concentration of bacteria and the diffusivity of different DOM substances, and within each population, the growth benefit from phycospheres is experienced by only a small fraction of cells. By informing a DOM utilization model with highly resolved behavioral data, the hybrid approach used here represents a new path toward the elusive goal of predicting the consequences of microscale interactions in the ocean. PMID:26802122

  5. Pyrolysis-combustion 14C dating of soil organic matter

    USGS Publications Warehouse

    Wang, Hongfang; Hackley, Keith C.; Panno, S.V.; Coleman, D.D.; Liu, J.C.-L.; Brown, J.

    2003-01-01

    Radiocarbon (14C) dating of total soil organic matter (SOM) often yields results inconsistent with the stratigraphic sequence. The onerous chemical extractions for SOM fractions do not always produce satisfactory 14C dates. In an effort to develop an alternative method, the pyrolysis-combustion technique was investigated to partition SOM into pyrolysis volatile (Py-V) and pyrolysis residue (Py-R) fractions. The Py-V fractions obtained from a thick glacigenic loess succession in Illinois yielded 14C dates much younger but more reasonable than the counterpart Py-R fractions for the soil residence time. Carbon isotopic composition (??13C) was heavier in the Py-V fractions, suggesting a greater abundance of carbohydrate- and protein-related constituents, and ??13C was lighter in the Py-R fractions, suggesting more lignin- and lipid-related constituents. The combination of 14C dates and ??13C values indicates that the Py-V fractions are less biodegradation resistant and the Py-R fractions are more biodegradation resistant. The pyrolysis-combustion method provides a less cumbersome approach for 14C dating of SOM fractions. With further study, this method may become a useful tool for analyzing unlithified terrestrial sediments when macrofossils are absent. ?? 2003 University of Washington. Published by Elsevier Inc. All rights reserved.

  6. Natural organic matter enhanced mobility of nano zerovalent iron.

    PubMed

    Johnson, Richard L; Johnson, Graham O'Brien; Nurmi, James T; Tratnyek, Paul G

    2009-07-15

    Column studies showed that the mobility of nanometer-sized zerovalent iron (nZVI) through granular media is greatly increased in the presence of natural organic matter (NOM). At NOM concentrations of 20 mg/L or greater, the nZVI was highly mobile during transport experiments in 0.15-m long columns packed with medium sand. Below 20 mg/L NOM, mobility of the nZVI was less; however, even at 2 mg/L the nZVI showed significantly increased mobility compared to the no-NOM case. Spectrophotometric and aggregation studies of nZVI suspensions in the presence of NOM suggest that sorption of the NOM onto the nZVI, resulting in a reduced sticking coefficient, may be the primary mechanism of enhanced mobility. Modeling the mobility of nZVI in porous media with filtration theory is challenging, but calibration of a simple model with experimental results from the column experiments reported here allows simulation of transport distances during injection. The simulation results show that the increased mobility due to NOM combined with the decrease in mobility due to decreased velocity with distance from an injection well could produce an injection zone that is wide enough to be useful for remediation but small enough to avoid reaching unwanted receptors. PMID:19708381

  7. The chemical ecology of soil organic matter molecular constituents.

    PubMed

    Simpson, Myrna J; Simpson, André J

    2012-06-01

    Soil organic matter (OM) contains vast stores of carbon, and directly supports microbial, plant, and animal life by retaining essential nutrients and water in the soil. Soil OM plays important roles in biological, chemical, and physical processes within the soil, and arguably plays a major role in maintaining long-term ecological stability in a changing world. Despite its importance, there is a great deal still unknown about soil OM chemical ecology. The development of sophisticated analytical methods have reshaped our understanding of soil OM composition, which is now believed to be comprised of plant and microbial products at various stages of decomposition. The methods also have recently been applied to study environmental change in various settings and have provided unique insight with respect to soil OM chemical ecology. The goal of this review is to highlight the methods used to characterize soil OM structure, source, and degradation that have enabled precise observations of OM and associated ecological shifts. Although the chemistry of soil OM is important in its overall fate in ecosystems, the studies conducted to date suggest that ecological function is not defined by soil OM chemistry alone. The long-standing questions regarding soil OM stability and recalcitrance will likely be answered when several molecular methods are used in tandem to closely examine structure, source, age, degradation stage, and interactions of specific OM components in soil.

  8. Mercury reduction and complexation by natural organic matter

    SciTech Connect

    Gu, Baohua; Bian, Yongrong; Miller, Carrie L; Dong, Wenming; Jiang, Xin; Liang, Liyuan

    2011-01-01

    Mercuric Hg(II) species form complexes with natural dissolved organic matter (DOM) such as humic acid (HA), and this binding is known to affect the chemical and biological transformation and cycling of mercury in aquatic environments. Dissolved elemental mercury, Hg(0), is also widely observed in sediments and water. However, reactions between Hg(0) and DOM have rarely been studied in anoxic environments. Here, under anoxic dark conditions we show strong interactions between reduced HA and Hg(0) through thiol-ligand induced oxidative complexation with an estimated binding capacity of about 3.5 umol Hg(0)/g HA and a partitioning coefficient greater than 10^6 mL/g. We further demonstrate that Hg(II) can be effectively reduced to Hg(0) in the presence of as little as 0.2 mg/L reduced HA, whereas production of purgeable Hg(0) is inhibited by complexation as HA concentration increases. This dual role played by DOM in the reduction and complexation of mercury is likely widespread in anoxic sediments and water and can be expected to significantly influence the mercury species transformations and biological uptake that leads to the formation of toxic methylmercury.

  9. Biochemical composition of organic matter in UK Midlands catchments: implications for drinking water treatment

    NASA Astrophysics Data System (ADS)

    Bieroza, M.; Bridgeman, J.; Baker, A.

    2007-12-01

    Insufficient removal of natural organic matter at treatment works can lead to the formation of potentially carcinogenic disinfection by-products (mainly trihalomethanes and haloacetic acids, THMs and HAAs) due to reactions of residual organic matter with chlorine added at the disinfection stage of water treatment process. However, the total organic carbon (TOC) removal efficiency is controlled by the content and character of organic matter in treated water, spatially and temporally dependent (e.g. the ratio of hydrophylic and hydrophobic fractions). Thus, a better understanding of organic matter composition can affect the treatment process strategies, improving the THM formation prediction and the quantification of coagulant and disinfection dosages. Fluorescence analysis of organic matter composition and treatment efficiency has been carried out on raw and partially-treated water samples from catchments in the Midlands region of the UK. The catchments cover an area of different water sources, ranging from upland, peaty-rich subcatchments with coloured, young waters, to agriculturally transformed lowland subcatchments. From the spectrophotometric analysis of raw water it was found that, the abstraction from river with water storage in reservoirs corresponds with a hydrophilic character of organic matter, rather high microbial fraction and high TOC. Opposite properties (hydrophobic, low microbial and variable TOC) are specific for sites with abstraction and storage processes within reservoirs. For direct abstraction from rivers, without water storing in reservoir, a common pattern is intermediate character of organic matter. The fluorescence excitation-emission matrix (EEM) technique was used for the assessment of water treatment works performance (TOC removal) and organic matter characterization. The freshwater organic matter exhibits specific fluorescence properties, with increased intensities of fluorescence in some regions of the EEM, resulting from the water

  10. Occurrence and abundance of carbohydrates and amino compounds in sequentially extracted labile soil organic matter fractions.

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This study aimed to investigate the content of carbohydrates and amino compounds in three labile fraction of soil organic matter (SOM). Soil samples were collected from two agricultural fields in southern Italy and the light fraction (LF), the 500–53-µm particulate organic matter (POM) and the mobil...

  11. Contribution of plant lignin to the soil organic matter formation and stabilization

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Lignin is the third most abundant plant constituent after cellulose and hemicellulose and thought to be one of the building blocks for soil organic matter formation. Lignin can be used as a predictor for long-term soil organic matter stabilization and C sequestration. Soils and humic acids from fo...

  12. FACTORS INFLUENCING PHOTOREACTIONS OF DISSOLVED ORGANIC MATTER IN A COASTAL RIVER OF THE SOUTHEASTERN UNITED STATES

    EPA Science Inventory

    Photoreactions of dissolved organic matter can affect the oxidizing capacity, nutrient dynamics, trace gas exchange, and color of surface waters. This study focuses on factors that affect the photoreactions of the colored dissolved organic matter (CDOM) in the Satilla River, a co...

  13. Advances in understanding the molecular structure of soil organic matter: Implications for interactions in the environment

    EPA Science Inventory

    We take a historic approach to explore how concepts of the chemical and physical nature of soil organic matter have evolved over time. We emphasize conceptual and analytical achievements in organic matter research over the last two decades and demonstrate how these developments h...

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

    PubMed

    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.

  15. Abiotic emissions of methane and reduced organic compounds from organic matter

    NASA Astrophysics Data System (ADS)

    Roeckmann, T.; Keppler, F.; Vigano, I.; Derendorp, L.; Holzinger, R.

    2012-12-01

    Recent laboratory studies show that the important greenhouse gas methane, but also other reduced atmospheric trace gases, can be emitted by abiotic processes from organic matter, such as plants, pure organic compounds and soils. It is very difficult to distinguish abiotic from biotic emissions in field studies, but in laboratory experiments this is easier because it is possible to carefully prepare/sterilize samples, or to control external parameters. For example, the abiotic emissions always show a strong increase with temperature when temperatures are increased to 70C or higher, well above the temperature optimum for bacterial activity. UV radiation has also been clearly shown to lead to emission of methane and other reduced gases from organic matter. Interesting information on the production mechanism has been obtained from isotope studies, both at natural abundance and with isotope labeling. For example, the methoxyl groups of pectin were clearly identified to produce methane. However, analysis of the isotopic composition of methane from natural samples clearly indicates that there must be other molecular mechanisms that lead to methane production. Abiotic methane generation could be a ubiquitous process that occurs naturally at low rates from many different sources.

  16. Soil organic matter on citrus plantation in Eastern Spain

    NASA Astrophysics Data System (ADS)

    Cerdà, Artemi; Pereira, Paulo; Novara, Agata; Prosdocimi, Massimo

    2015-04-01

    Citrus plantations in Eastern Spain are the main crop and Valencia region is the largest world exporter. The traditional plantation are located on flood irrigated areas and the new plantation are located on slopes were drip irrigation is the source of the wetting. It has been demonstrate that the citrus plantations contribute to high erosion rates on slopes (Cerdà et al., 2009b) as it is usual on agriculture land (Cerdà et al., 2009a), but when organic farming is present the soil erosion is much lower (Cerdà and Jurgensen, 2008; Cerdà et al., 2009; Cerdà and Jurgensen, 2011). This is a worldwide phenomenon (Wu et al., 2007; Wu et al., 2011; Xu et al., 2010; Xu et al., 2012a; Xu et al., 2012b), which are a key factor of the high erosion rates in rural areas (García Orenes et al., 2009: García Orenes et al., 20010; García Orenes et al., 2012; Haregewyn et al., 2013; Zhao et al., 2013). The key factor of the contrasted response of soils to the rain in citrus is the organic matter cover. This is why the Soil Erosion and Degradation Research Team developed a survey to determine the soil erosion rates on citrus orchards under different managements. A hundred of samples were collected in a citrus plantation on slope under conventional management (Chemical management), one on organic farming, one on traditional flood irrigated organic farming and one on traditional chemical flooding farm. The organic farming soils were treated with 10000 Kg ha-1 of manure yearly. The results show that the mean soil organic matter content was 1.24 %, 3.54%, 5,43% and 2.1% respectively, which show a clear impact of organic farming in the recovery of the soil organic matter. meanwhile the on the slopes and the flood-irrigated soils are Acknowledgements The research projects GL2008-02879/BTE, LEDDRA 243857 and PREVENTING AND REMEDIATING DEGRADATION OF SOILS IN EUROPE THROUGH LAND CARE (RECARE)FP7- ENV-2013- supported this research. References Cerdà, A., Flanagan, D.C., le Bissonnais

  17. Where is DNA preserved in soil organic matter?

    NASA Astrophysics Data System (ADS)

    Zaccone, Claudio; Beneduce, Luciano; Plaza, César

    2015-04-01

    Deoxyribonucleic acid (DNA) consists of long chains of alternating sugar and phosphate residues twisted in the form of a helix. Upon decomposition of plant and animal debris, this nucleic acid is released into the soil, where its fate is still not completely understood. In fact, although DNA is one of the organic compounds from living cells that is apparently broken down rapidly in soils, it is also potentially capable of being incorporated in (or interact with) the precursors of humic molecules. In order to track DNA occurrence in soil organic matter (SOM) fractions, an experiment was set up as a randomized complete block design with two factors, namely biochar addition and organic amendment. In particular, biochar (BC), applied at a rate of 20 t/ha, was combined with municipal solid waste compost (BC+MC) at a rate equivalent to 75 kg/ha of potentially available N, and with sewage sludge (BC+SS) at a rate equivalent to 75 kg/ha of potentially available N. Using a physical fractionation method, free SOM located between aggregates (unprotected C pool; FR), SOM occluded within macroaggregates (C pool weakly protected by physical mechanisms; MA), SOM occluded within microaggregates (C pool strongly protected by physical mechanisms; MI), and SOM associated with the mineral fractions (chemically-protected C pool; MIN) were separated from soil samples. DNA was then isolated from each fraction of the two series, as well as from the unamended soil (C) and from the bulk soils (WS), using Powersoil DNA isolation kit (MoBio, CA, USA) with a modified protocol. Data clearly show that the DNA survived the SOM fractionation, thus suggesting that physical fractionation methods create less artifacts compared to the chemical ones. Moreover, in both BC+MC and BC+SS series, most of the isolated DNA was present in the FR fraction, followed by the MA and the MI fractions. No DNA was recovered from the MIN fraction. This finding supports the idea that most of the DNA occurring in the SOM

  18. Soil Organic Matter Effects on Phosphorus Sorption: a Path Analysis

    SciTech Connect

    Kang, J.; Hesterberg, D; Osmond, D

    2009-01-01

    While P sorption in mineral soils has been extensively studied, P sorption behavior in organic-rich soils is less known. This study was conducted to determine the relationships between Langmuir P sorption maxima (S{sub max}) and selected physicochemical properties of soils, with particular emphasis on organic matter (OM) content. The S{sub max} values were determined for 72 soil samples from the North Carolina Coastal Plain, along with pH, clay and OM contents, oxalate-extractable P (P{sub ox}), Al (Al{sub ox}), and Fe (Fe{sub ox}), and Mehlich 3 extractable P (P{sub M3}), Al (Al{sub M3}), and Fe (Fe{sub M3}). Path analysis was used to examine direct and indirect effects of soil properties on S{sub max}. In the oxalate path analysis, the direct effects of clay, Al{sub ox}, and Fe{sub ox} on S{sub max} were significant in the order Al{sub ox} > clay > Fe{sub ox} (P < 0.05). The S{sub max} was highly influenced by the indirect effect of Al{sub ox} and Fe{sub ox} through OM content. A two-piece segmented linear relationship existed between S{sub max} and OM and the regression slope in soils with OM {le} 49 g kg{sup -1} was 10-fold greater than that for soils with OM > 49 g kg{sup -1}. This finding suggested that noncrystalline or organically bound Al and Fe in the soils with OM > 49 g kg{sup -1} is less effective for P sorption than in the soils with lower OM content. In the Mehlich 3 path analysis, the direct effects of clay, OM, and Al{sub M3} on S{sub max} were significant in the order Al{sub M3} > OM > clay (P < 0.05) while the direct effect of Fe{sub M3} on S{sub max} was not significant. Oxalate may be better suited than Mehlich 3 as an extractant for predicting P sorption capacity in the Coastal Plain soils.

  19. Biogeochemistry of dissolved organic matter in an anoxic intertidal creek bank

    NASA Astrophysics Data System (ADS)

    Seidel, Michael; Beck, Melanie; Riedel, Thomas; Waska, Hannelore; Suryaputra, I. G. N. A.; Schnetger, Bernhard; Niggemann, Jutta; Simon, Meinhard; Dittmar, Thorsten

    2014-09-01

    Seawater circulation in permeable coastal sediments is driven by tidal changes in hydraulic gradients. The resulting submarine groundwater discharge is a source of nutrients and dissolved organic matter (DOM) to the water column. Yet, little is known about the cycling of DOM within tidal sediments, because the molecular DOM characterization remains analytically challenging. One technique that can dissect the multitude of molecules in DOM is ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). To aim at a high resolution DOM analysis we study the seasonal turnover and marine and terrestrial sources of DOM in an intertidal creek bank of the southern North Sea down to 3 m depth and link the biogeochemical processes to FT-ICR-MS data and the analyses of inorganic porewater chemistry, δ13C of solid-phase extracted dissolved organic carbon (SPE-DOC), dissolved black carbon (DBC) and dissolved carbohydrates (DCHO). Increasing concentrations of dissolved Fe, Mn, P, total alkalinity, dissolved nitrogen, DOC and a concomitant decrease of sulfate along the seawater circulation path from the upper tidal flat to the tidal flat margin indicate continuous microbial activity. The relative increase of Si concentrations, unsaturated aliphatics, peptide molecular formulae and isotopically more 13C-enriched SPE-DOC towards the tidal flat margin suggests that remineralization processes mobilize DOM from buried algal (diatoms) and microbial biomass. Porewater in sediments <100 cm depth contains 13C-depleted SPE-DOC and highly unsaturated compounds which are probably derived from eroded peats, suggesting rapid removal of bioavailable marine DOM such as DCHO from the water column and selective enrichment of terrestrial DOM. DBC concentrations are highest in the discharging porewater close to the tidal creek suggesting that the intertidal flat is an important DBC source to the coastal ocean. Porewater DOM accumulating at the low water line is

  20. Sources and preservation of sedimentary organic matter in the Southern Bohai Sea and the Yellow Sea: evidence from lipid biomarkers.

    PubMed

    Lin, Tian; Wang, Lifang; Chen, Yingjun; Tian, Chongguo; Pan, Xiaohui; Tang, Jianhui; Li, Jun

    2014-09-15

    The region of Southern Bohai Sea (SBS) and Yellow Sea (YS) represents one of the best examples of large river-dominated ocean margins. The transport and accumulation of sediments played a primary role in distribution of the lipids in the region and could lead to a preferential accumulation of these more refractory land-based lipids. The spatial distribution of total organic carbon (TOC) matched with the lipid distributions over the shelf, and high TOC presented in the central YS, but TOC burial fluxes decreased from 110 ton/km(2)/yr of SBS to 25-32 ton/km(2)/yr of YS. Good correlations were observed between terrestrial n-alkanes and TOC in the sediments of SBS and northern YS, but they were poor for southern YS, meanwhile higher ratios of nC27+nC29+nC31/nC15+nC17+nC19 (12±6) were observed in SBS, and lower in YS (2.2±1.0), suggesting the Yellow River discharge was an important source of terrestrial organic matter to the shelf.

  1. Reflectance spectroscopy of natural organic solids, iron sulfides and their mixtures as refractory analogues for Rosetta/VIRTIS' surface composition analysis of 67P/CG

    NASA Astrophysics Data System (ADS)

    Moroz, Lyuba V.; Markus, Kathrin; Arnold, Gabriele; Henckel, Daniela; Kappel, David; Schade, Ulrich; Rousseau, Batiste; Quirico, Eric; Schmitt, Bernard; Capaccioni, Fabrizio; Bockelee-Morvan, Dominique; Filacchione, Gianrico; Érard, Stéphane; Leyrat, Cedric; VIRTIS Team

    2016-10-01

    Analysis of 0.25-5 µm reflectance spectra provided by the Visible and InfraRed Thermal Imaging Spectrometer (VIRTIS) onboard Rosetta orbiter revealed that the surface of 67P/CG is dark from the near-UV to the IR and is enriched in refractory phases such as organic and opaque components. The broadness and complexity of the ubiquitous absorption feature around 3.2 µm suggest a variety of cometary organic constituents. For example, complex hydrocarbons (aliphatic and polycyclic aromatic) can contribute to the feature between 3.3 and 3.5 µm and to the low reflectance of the surface in the visible. Here we present the 0.25-5 µm reflectance spectra of well-characterized terrestrial hydrocarbon materials (solid oil bitumens, coals) and discuss their relevance as spectral analogues for a hydrocarbon part of 67P/CG's complex organics. However, the expected low degree of thermal processing of cometary hydrocarbons (high (H+O+N+S)/C ratios and low carbon aromaticities) suggests high IR reflectance, intense 3.3-3.5 µm absorption bands and steep red IR slopes that are not observed in the VIRTIS spectra. Fine-grained opaque refractory phases (e.g., iron sulfides, Fe-Ni alloys) intimately mixed with other surface components are likely responsible for the low IR reflectance and low intensities of absorption bands in the VIRTIS spectra of the 67P/CG surface. In particular, iron sulfides are common constituents of cometary dust, "cometary" chondritic IDPs, and efficient darkening agents in primitive carbonaceous chondrites. Their effect on reflectance spectra of an intimate mixture is strongly affected by grain size. We report and discuss the 0.25-5 µm reflectance spectra of iron sulfides (meteoritic troilite and several terrestrial pyrrhotites) ground and sieved to various particle sizes. In addition, we present reflectance spectra of several intimate mixtures of powdered iron sulfides and solid oil bitumens. Based on the reported laboratory data, we discuss the ability of

  2. Quantitative retrieving of soil organic matter using field spectrometer and hyperspectral remote sensing

    NASA Astrophysics Data System (ADS)

    Zhuo, Luo; Liu, Yaolin; Chen, Jie; Hu, Changji; Wu, Jian

    2008-12-01

    As the important component of soil, soil organic matter not only provides every nutrient element for crop, but also has determinant effect for forming of soil structure and melioration the soil physical character. Mapping and dating soil organic matter is of great importance in soil use and evaluation. In this study we examine the feasibility of soil organic matter content by using Hyperspectrally reflective remote sensing methodology. This technique was tested in Xiaochang County located in Hubei province. The soil reflectance properties of samples were measured in the laboratory by ASD field spectrometer. The correlation analysis related with organic matter content was processed from three factors: the spectral reflectance parameter ((lgρ)', ρ/ ρ450-750 and (1/lgρ623)'/ (1/lgρ564)'). The results show that the correlation coefficients of r values were: organic matter identification index (ρ/ ρ450-750) > logarithmic first derivative of reflectivity ((lgρ)') > organic matter mix identification index ((1/lgρ623)'/(1/lgρ564)'). Knowing these correlations we were able to use the best prominence correlation of organic matter identification index of 1850nm wavelength as the variable regression to build up statistical regression analysis. We used five model types (Linear Function, Logarithmic Function, Quadratic Function, Power Function and Exponential Function) to forecast the soil organic matter content Hyperion model. The accuracy assessment (R2= 0.8484) by relating forecasted organic matter values with Quadratic Function regression showed that the model is reliable and significantly correlative with known stabilization processes throughout the study area. The quantitative methodology developed in this study for refutations soil organic matter content can be adapted to other regions throughout the world.

  3. Estimating toxic damage to soil ecosystems from soil organic matter profiles

    USGS Publications Warehouse

    Beyer, W.N.

    2001-01-01

    Concentrations of particulate and total organic matter were measured in upper soil profiles at 26 sites as a potential means to identify toxic damage to soil ecosystems. Because soil organic matter plays a role in cycling nutrients, aerating soil, retaining water, and maintaining tilth, a significant reduction in organic matter content in a soil profile is not just evidence of a change in ecosystem function, but of damage to that soil ecosystem. Reference sites were selected for comparison to contaminated sites, and additional sites were selected to illustrate how variables other than environmental contaminants might affect the Soil organic matter profile. The survey was undertaken on the supposition that environmental contaminants and other stressors reduce the activity of earthworms and other macrofauna, inhibiting the incorporation of organic matter into the soil profile. The profiles of the unstressed soils showed a continuous decrease in organic matter content from the uppermost mineral soil layer (0-2.5 cm) down to 15 cm. Stressed soils showed an abrupt decrease in soil organic matter content below a depth of 2.5 cm. The 2.5-5.0 cm layer of stressed soils--such as found in a pine barren, an orchard, sites contaminated with zinc, and a site with compacted soil--had less than 4% total organic matter and less than 1% particulate organic matter. However, damaged soil ecosystems were best identified by comparison of their profiles to the profiles of closely matched reference soils, rather than by comparison to these absolute values. The presence or absence of earthworms offered a partial explanation of observed differences in soil organic matter profiles.

  4. Transport of organic contaminants in subsoil horizons and effects of dissolved organic matter related to organic waste recycling practices.

    PubMed

    Chabauty, Florian; Pot, Valérie; Bourdat-Deschamps, Marjolaine; Bernet, Nathalie; Labat, Christophe; Benoit, Pierre

    2016-04-01

    Compost amendment on agricultural soil is a current practice to compensate the loss of organic matter. As a consequence, dissolved organic carbon concentration in soil leachates can be increased and potentially modify the transport of other solutes. This study aims to characterize the processes controlling the mobility of dissolved organic matter (DOM) in deep soil layers and their potential impacts on the leaching of organic contaminants (pesticides and pharmaceutical compounds) potentially present in cultivated soils receiving organic waste composts. We sampled undisturbed soil cores in the illuviated horizon (60-90 cm depth) of an Albeluvisol. Percolation experiments were made in presence and absence of DOM with two different pesticides, isoproturon and epoxiconazole, and two pharmaceutical compounds, ibuprofen and sulfamethoxazole. Two types of DOM were extracted from two different soil surface horizons: one sampled in a plot receiving a co-compost of green wastes and sewage sludge applied once every 2 years since 1998 and one sampled in an unamended plot. Results show that DOM behaved as a highly reactive solute, which was continuously generated within the soil columns during flow and increased after flow interruption. DOM significantly increased the mobility of bromide and all pollutants, but the effects differed according the hydrophobic and the ionic character of the molecules. However, no clear effects of the origin of DOM on the mobility of the different contaminants were observed.

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

    NASA Astrophysics Data System (ADS)

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

    2015-06-01

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

  6. Non-targeted Explorations in the Compositional and Structural Space of Natural Organic Matter

    NASA Astrophysics Data System (ADS)

    Hertkorn, N.; Schmitt-Kopplin, P.; Perdue, E. M.

    2009-05-01

    Natural organic matter (NOM) occurs in soils, freshwater and marine environments, in the atmosphere and in the form of prebiotic organic matter and represents an exceedingly complex mixture of organic compounds that collectively exhibits a nearly continuous range of properties (size-reactivity continuum). The fate NOM in the bio- and geosphere is governed according to the rather fundamental restraints of thermodynamics and kinetics. In these intricate materials, the "classical" signatures of the (geogenic or ultimately biogenic) precursor molecules, like lipids, glycans, proteins and natural products have been attenuated, often beyond recognition, during a succession of biotic and abiotic (e.g. photo- and redox chemistry) reactions. Because of this loss of biochemical signature, these materials can be designated non- repetitive complex systems. The most informative, "bottom-up" approach to molecularly characterize these complex materials necessarily relies upon spectroscopic methods which translate high-precision frequency measurements into very significant molecular-level information. Frequencies can be measured with an accuracy of 15 digits. This extent of accuracy in frequency measurements translates directly into high resolution, itself a very useful and even indispensable feature to produce information-rich data with sufficient resolution to overcome the otherwise common and detrimental effects of intrinsic averaging, which deteriorate spectral resolution to the degree of a bulk-type characterization rather than to a molecular resolution analysis. High-precision frequency measurements, which can be translated into isotope-specific molecular resolution detail of unprecedented significance and richness, define the core of the two most influential methods of organic structural spectroscopy for the investigation of complex materials, namely NMR spectroscopy (provide unsurpassed insight into close-range molecular order to assess the structural space) and FTICR mass

  7. Role of organic matter fractions in the Montney tight gas reservoir quality

    NASA Astrophysics Data System (ADS)

    Sanei, Hamed; Wood, James M.; Haeri Ardakani, Omid; Clarkson, Chris R.

    2015-04-01

    This study presents a new approach in Rock-Eval analysis to quantify various organic matter fractions in unconventional reservoirs. The results of study on core samples from the Triassic Montney Formation tight gas reservoir in the Western Canadian Sedimentary Basin show that operationally-defined S1 and S2 hydrocarbon peaks from conventional Rock-Eval analysis may not adequately characterize the organic constituents of unconventional reservoir rocks. Modification of the thermal recipe for Rock-Eval analysis, in conjunction with manual peak integration, provides important information with significance for the evaluation of reservoir quality. An adapted Rock-Eval method, herein called the extended slow heating (ESH) cycle, was developed in which the heating rate was slowed to 10°C per minute over an extended temperature range (150 to 650°C). For Montney core samples from the wet gas window, this method provided quantitative distinctions between major organic matter components of the rock. We show that the traditional S1 and S2 peaks can now be quantitatively divided into three components: (S1ESH) free light oil, (S2a ESH) condensed hydrocarbon residue (CHCR), and (S2b ESH + residual carbon) solid bitumen (refractory, consolidated bitumen/pyrobitumen). The majority of the total organic carbon (TOC) in the studied Montney core samples consists of solid bitumen that represents a former liquid oil phase which migrated into the larger paleo-intergranular pore spaces. Subsequent physicochemical changes to the oil environment led to the precipitation of asphaltene aggregates. Further diagenetic and thermal maturity processes consolidated these asphaltene aggregates into "lumps" of solid bitumen (or pyrobitumen at higher thermal maturity). Solid bitumen obstructs porosity and hinders fluid flow, and thus shows strong negative correlations with reservoir qualities such as porosity and pore throat size. We also find a strong positive correlation between the quantities of

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

    NASA Astrophysics Data System (ADS)

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

    2009-04-01

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

  9. Organic matter formed from hydrolysis of metal carbides of the iron peak of cosmic elemental abundance

    NASA Astrophysics Data System (ADS)

    Cataldo, Franco

    2003-01-01

    This work is a modern revisitation of an old idea of great chemists of the past such as Berthelot, Mendeleev, Cloez and Moissan: the formation of organic matter under pre-biotic conditions starting from the hydrolysis of metal carbides. This idea was originally proposed for the formation of petroleum in the Earth and was extended to other bodies of the solar system by Sokolov at the end of the 19th century. The reason for this revisitation lies in the fact that complex organic matter resembling a petroleum fraction may exist in certain protoplanetary nebulae. The present work starts with a survey of the theory of the inorganic origin of petroleum and reports on current evidence for its derivation from residues of formerly living matter, but also considers theories that admit both a biogenic and an abiogenic origin for petroleum. By considering the cosmic abundance of elements and the evidence concerning the presence of carbides in meteorites, we discuss the formation, structure and hydrolysis products derived from the metal carbides of the iron peak of cosmic elemental abundance. Chromium carbide (Cr3C2) has then been used as a model compound for all the key carbides of the iron peak of the cosmic abundance (Cr, Fe, Ni, V, Mn, Co) and it has been hydrolysed under different conditions and the hydrocarbons formed have been analysed using electronic spectroscopy, high-performance liquid chromatography with a diode-array detector (HPLC-DAD) and by Fourier-transform infrared (FT-IR) spectroscopy. Methane, a series of about 20 different alkenes with single and conjugated double bonds have been detected. Paraffins are formed simultaneously with the alkene series but no acetylenic hydrocarbons have been detected. This study confirms early works considering the easy hydrolysis of the carbides of Cr, Fe, Ni, Mn and Co with the formation of H2, a series of alkanes including methane and a series of alkenes including ethylene. The peculiar behaviour of copper carbide (copper is

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

    USGS Publications Warehouse

    Schmoker, J.W.

    1981-01-01

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

  11. Jellyfish Lake, Palau: early diagenesis of organic matter in sediments of an anoxic marine lake

    USGS Publications Warehouse

    Orem, W.H.; Burnett, W.C.; Landing, W.M.; Lyons, W.B.; Showers, W.

    1991-01-01

    The major postdepositional change in the sedimentary organic matter is carbohydrate biodegradation. Lignin and aliphatic substances are preserved in the sediments. Dissolved organic matter in pore waters is primarily composed of carbohydrates, reflecting the degradation of sedimentary carbohydrates. Rate constants for organic carbon degradation and sulfate reduction in sediments of the lake are about 10?? lower than in other anoxic sediments. This may reflect the vascular plant source and partly degraded nature of the organic matter reaching the sediments of the lake. -from Authors

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

    USGS Publications Warehouse

    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

  13. Nanoscale Structure of Organic Matter Could Explain Litter Decomposition

    NASA Astrophysics Data System (ADS)

    Papa, G.; Adani, F.

    2014-12-01

    According to the literature biochemical catalyses are limited in their actions because of the complex macroscopic and, above all, microscopic structures of cell wall that limit mass transportation (i.e. 3D structure). Our study on energy crop showed that plant digestibility increased by modifying the 3D cell wall microstructure. Results obtained were ascribed to the enlargement, such as effectively measured, of the pore spaces between cellulose fibrils. Therefore we postulated that 3 D structure of plant residues drives degradability in soil determining its recalcitrance in short time. Here we focused on the drivers of short-term decomposition of organic matter (plant residues) in soils evaluating the architecture of plant tissues, captured via measurements of the microporosiy of the cell walls. Decomposition rates of a wide variety of biomass types were studied conducting experiments in both aerobic and anaerobic environments. Different analytical approaches were applied in order to characterize biomass at both chemical and physical level. Combined statistical approaches were used to examine the relationships between carbon mineralization and chemical/physical characteristics. The results revealed that degradation was significantly and negatively correlated with the micro-porosity surface (MiS) (surface of pores of 0.3-1.5 nm of diameter). The multiple regressions performed by using partial least square model enabled describing biomass biodegradability under either aerobic and anaerobic condition by using micro-porosity and aromatic-C content (assumed to be representative of lignin) as independent variables (R2 =0.97, R2cv =0.95 for aerobic condition; R2 =0.99, R2cv =0.98 for anaerobic condition, respectively). These results corroborate the hypothesis that plant tissues are physically protected from enzymatic attack by a microporous "sheath" that limit penetration into cell wall, and demonstrate the key role played by aromatic carbon, because of its chemical

  14. Hydrological controls on rate of organic matter mineralization in peats

    NASA Astrophysics Data System (ADS)

    Ghezzehei, Teamrat; Arnold, Chelsea; Asefaw Berhe, Asmeret

    2016-04-01

    The predominant factor that ties together the formation and persistence of peat soils across regions is their dependence on localized hydrology. Hydrology also plays a dominant role in the relative strength of peatlands as sinks for atmospheric carbon dioxide and sources of methane, and thus on peatland net climate impact. Drying of peat soils by climate change and/or drainage is typically followed by reduction in methane emissions. However, this may easily be offset by the increase in carbon dioxide production. Therefore, mechanistic understanding of peatland hydrology and its association with carbon cycling is a prerequisite for assessing vulnerability of peats to disturbances and for incorporating the associated feedbacks in carbon-climate models. We will present physically based model that ties together the structure of peat soils (mainly pore size distribution and mechanical stability) to rates of aerobic and anaerobic decomposition over a wide range of soil water potentials. Peats consist of hierarchical structure with clear separation of the pores into a population of micropores within clumps of organic matter and/or soil aggregates and a group of macropores between clumps and/or aggregates. This essentially partitions the carbon stock in peat soils in to multiple pools that become mineralizable at disparate water potential ranges. While the carbon in macropores can readily be decomposed by aerobic microorganisms when the soil is only slightly drained, the carbon in fine pores remains largely protected from aerobic microbes until the water potential exceeds a threshold that lets in oxygen. In this presentation we will show the mathematical development of the model and illustrative examples that compare projections with data derived from the literature.

  15. Concurrent photolytic degradation of aqueous methylmercury and dissolved organic matter

    USGS Publications Warehouse

    Fleck, Jacob A.; Gill, Gary W.; Bergamaschi, Brian A.; Kraus, Tamara E.C.; Downing, Bryan D.; Alpers, Charles N.

    2014-01-01

    Monomethyl mercury (MeHg) is a potent neurotoxin that threatens ecosystem viability and human health. In aquatic systems, the photolytic degradation of MeHg (photodemethylation) is an important component of the MeHg cycle. Dissolved organic matter (DOM) is also affected by exposure to solar radiation (light exposure) leading to changes in DOM composition that can affect its role in overall mercury (Hg) cycling. This study investigated changes in MeHg concentration, DOM concentration, and the optical signature of DOM caused by light exposure in a controlled field-based experiment using water samples collected from wetlands and rice fields. Filtered water from all sites showed a marked loss in MeHg concentration after light exposure. The rate of photodemethylation was 7.5 × 10-3 m2 mol-1 (s.d. 3.5 × 10-3) across all sites despite marked differences in DOM concentration and composition. Light exposure also caused changes in the optical signature of the DOM despite there being no change in DOM concentration, indicating specific structures within the DOM were affected by light exposure at different rates. MeHg concentrations were related to optical signatures of labile DOM whereas the percent loss of MeHg was related to optical signatures of less labile, humic DOM. Relationships between the loss of MeHg and specific areas of the DOM optical signature indicated that aromatic and quinoid structures within the DOM were the likely contributors to MeHg degradation, perhaps within the sphere of the Hg-DOM bond. Because MeHg photodegradation rates are relatively constant across freshwater habitats with natural Hg–DOM ratios, physical characteristics such as shading and hydrologic residence time largely determine the relative importance of photolytic processes on the MeHg budget in these mixed vegetated and open-water systems.

  16. Biogeochemical Processes That Produce Dissolved Organic Matter From Wheat Straw

    USGS Publications Warehouse

    Wershaw, Robert L.; Rutherford, David W.; Leenheer, Jerry A.; Kennedy, Kay R.; Cox, Larry G.; Koci, Donald R.

    2003-01-01

    The chemical reactions that lead to the formation of dissolved organic matter (DOM) in natural waters are poorly understood. Studies on the formation of DOM generally are complicated because almost all DOM isolates have been derived from mixtures of plant species composed of a wide variety of different types of precursor compounds for DOM formation. This report describes a study of DOM derived mainly from bales of wheat straw that had been left in a field for several years. During this period of time, black water from the decomposing wheat straw accumulated in pools in the field. The nuclear magnetic resonance and infrared spectra of the black water DOM indicate that it is composed almost entirely of lignin and carbohydrate polymeric units. Analysis by high-performance size-exclusion chromatography with multi-angle laser-light scattering detection indicates that the number average molecular weight of the DOM is 124,000 daltons. The results presented in this report indicate that the black water DOM is composed of hemicellulose chains cross-linked to lignin oligomers. These types of structures have been shown to exist in the hemicellulose matrix of plant cell walls. The cross-linked lignin-hemicellulose complexes apparently were released from partially degraded wheat-straw cell walls with little alteration. In solution in the black water, these lignin-hemicellulose polymers fold into compact globular particles in which the nonpolar parts of the polymer form the interiors of the particles and the polar groups are on the exterior surfaces of the particles. The tightly folded, compact conformation of these particles probably renders them relatively resistant to microbial degradation. This should be especially the case for the aromatic lignin structures that will be buried in the interiors of the particles.

  17. Effects of Fe on Physicochemical Characteristics of Natural Organic Matter

    NASA Astrophysics Data System (ADS)

    Maurice, P. A.; Pullin, M. J.; Anthony, C.

    2003-12-01

    Natural organic matter (NOM) is ubiquitous in aquatic and terrestrial environments, and it plays an important role in controlling many biogeochemical processes. NOM molecular weight (MW) is a key property that affects NOM reactivity. Polyvalent metals such as Fe and Al bind strongly to NOM and also can cause its coagulation. Thus, we hypothesized that the presence of Fe would affect NOM MW determinations, even at relatively low Fe and NOM concentrations. This hypothesis was tested by adding increasing amounts of Fe(III) to aqueous solutions of NOM isolate (XAD-8) at pH 5.5, in the dark, and following changes in the NOM MW (measured by size exclusion chromatography), absorbance, and fluorescence. No change in MW was observed to 3 uM total Fe concentration, but at 10 uM total Fe concentration, there was a loss of low MW components and an increase in higher MW components. The weight average MW increased from 3661 Da to 3975 Da. Absorbance at 254 nm (typically monitored in water treatment processes) was unchanged by added Fe, but absorbance increase over parts of the visible spectrum (350-600 nm), and decreased in the far UV (200-225 nm), thus altering spectral slope. The two fluorescence maxima observed for this sample (Ex 325, Em 450; Ex 230, Em 435) decreased in intensity with increasing Fe concentration, with no shift in peak location. These results have important implications for our understanding of the concept of 'molecular weight' as applied to NOM, and for NOM reactivity including bioavailability, adsorption, and other processes.

  18. Spatial Arrangement of Organic Compounds on a Model Mineral Surface: Implications for Soil Organic Matter Stabilization

    NASA Astrophysics Data System (ADS)

    Ambaye, Haile; Petridis, Loukas; Jagadamma, Sindhu; Kilbey, Michael; Lauter, Valeria; Lokitz, Bradley; Mayes, Melanie

    2015-03-01

    Stability of organic carbon compounds in soil is important for global climate futures which could be affected by the complexity of the mineral-organic carbon interfaces. We examined the nanoscale structure of model interfaces by depositing films of organic carbon compounds of contrasting chemical character, hydrophilic glucose, deuterated-amphiphilic stearic acid (SA) and Natural Organic Matters (NOM) onto a soil mineral analogue (Al2O3) . The NOM was separated into its constituent components such as NOM-Philic and NOM-Phobic when it is deposited onto the soil mineral. We used Neutron Reflectivity technique to understand the depth organization of the thin films. The result indicates that glucose molecules reside in a layer between Al2O3 and stearic acid and SA self-assembles. No self-assembly of SA was observed when SA and NOM-Phobic was deposited on the mineral soil. Molecular dynamics simulations reveal the thermodynamic driving force behind glucose partitioning on the mineral interface. Funded by ORNL Director's Research and Development Program. Research at ORNL was sponsored by the BES, DOE.

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

    PubMed Central

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

    2015-01-01

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

  20. Natural organic matter and the event horizon of mass spectrometry.

    PubMed

    Hertkorn, N; Frommberger, M; Witt, M; Koch, B P; Schmitt-Kopplin, Ph; Perdue, E M

    2008-12-01

    Soils, sediments, freshwaters, and marine waters contain natural organic matter (NOM), an exceedingly complex mixture of organic compounds that collectively exhibit a nearly continuous range of properties (size-reactivity continuum). NOM is composed mainly of carbon, hydrogen, and oxygen, with minor contributions from heteroatoms such as nitrogen, sulfur, and phosphorus. Suwannee River fulvic acid (SuwFA) is a fraction of NOM that is relatively depleted in heteroatoms. Ultrahigh resolution Fourier transform ion cyclotron (FTICR) mass spectra of SuwFA reveal several thousand molecular formulas, corresponding in turn to several hundred thousand distinct chemical environments of carbon even without accountancy of isomers. The mass difference deltam among adjoining C,H,O-molecules between and within clusters of nominal mass is inversely related to molecular dissimilarity: any decrease of deltam imposes an ever growing mandatory difference in molecular composition. Molecular formulas that are expected for likely biochemical precursor molecules are notably absent from these spectra, indicating that SuwFA is the product of diagenetic reactions that have altered the major components of biomass beyond the point of recognition. The degree of complexity of SuwFA can be brought into sharp focus through comparison with the theoretical limits of chemical complexity, as constrained and quantized by the fundamentals of chemical binding. The theoretical C,H,O-compositional space denotes the isomer-filtered complement of the entire, very vast space of molecular structures composed solely of carbon, hydrogen, and oxygen. The molecular formulas within SuwFA occupy a sizable proportion of the theoretical C,H,O-compositional space. A 100 percent coverage of the theoretically feasible C,H,O-compositional space by SuwFA molecules is attained throughout a sizable range of mass and H/C and O/C elemental ratios. The substantial differences between (and complementarity of) the SuwFA molecular

  1. Colored dissolved organic matter in Tampa Bay, Florida

    USGS Publications Warehouse

    Chen, Z.; Hu, C.; Conmy, R.N.; Muller-Karger, F.; Swarzenski, P.

    2007-01-01

    Absorption and fluorescence of colored dissolved organic matter (CDOM) and concentrations of dissolved organic carbon (DOC), chlorophyll and total suspended solids in Tampa Bay and its adjacent rivers were examined in June and October of 2004. Except in Old Tampa Bay (OTB), the spatial distribution of CDOM showed a conservative relationship with salinity in June, 2004 (aCDOM(400) = − 0.19 × salinity + 6.78, R2 = 0.98, n = 17, salinity range = 1.1–32.5) with little variations in absorption spectral slope and fluorescence efficiency. This indicates that CDOM distribution was dominated by mixing. In October, 2004, CDOM distribution was nonconservative with an average absorption coefficient (aCDOM(400), ∼ 7.76 m-1) about seven times higher than that in June (∼ 1.11 m-1). The nonconservative behavior was caused largely by CDOM removal at intermediate salinities (e.g., aCDOM(400) removal > 15% at salinity ∼ 13.0), which likely resulted from photobleaching due to stronger stratification. The spatial and seasonal distributions of CDOM in Tampa Bay showed that the two largest rivers, the Alafia River (AR) and Hillsborough River (HR) were dominant CDOM sources to most of the bay. In OTB, however, CDOM showed distinctive differences: lower absorption coefficient, higher absorption spectral slopes, and lower ratios of CDOM absorption to DOC and higher fluorescence efficiency. These differences may have stemmed from (1) changes in CDOM composition by more intensive photobleaching due to the longer residence time of water mass in OTB; (2) other sources of CDOM than the HR/AR inputs, such as local creeks, streams, groundwater, and/or bottom re-suspension. Average CDOM absorption in Tampa Bay at 443 nm, aCDOM(443), was about five times higher in June and about ten times higher in October than phytoplankton pigment absorption, aph(443), indicating that blue light attenuation in the water column was dominated by CDOM rather than by phytoplankton absorption throughout the

  2. The Contribution of Fungal Necromass to Soil Organic Matter Storage

    NASA Astrophysics Data System (ADS)

    Schreiner, K. M.; Blair, N. E.; Buiser, A.; Egerton-Warburton, L.

    2013-12-01

    Saprotrophic fungi have the ability to degrade the three most important biopolymers: cellulose, lignin, and chitin, and therefore are key moderators of a globally important flow of carbon. However, little is known about how that carbon is transformed and/or stored in soil organic matter (SOM). Fungi are also known to produce a variety of biopolymers, such as chitin, melanin, glucan, and mucus-like exudates, and it is likely that these compounds contribute to long-term storage of SOM. In fact, recent work with ectomycorrhizal fungi has shown that a portion of the fungal necromass survives after degradation times of a few weeks to one month (e.g. Drigo et al. 2012, Clemmenson et al. 2013). Until now, the potential contribution of other abundant fungi to recalcitrant SOM has been unknown. Soil incubations have been performed with the common saprotrophic fungus, Fusarium avencum. Approximately 80% of the fungal material was found to turnover over on a time period of days, but 15% of the original biomass was left over at the end of the two-month degradation experiment in both laboratory experiments and in situ in the Dixon Prairie of the Chicago Botanic Garden. In both experiments, degradation was performed by a natural soil microbial consortium. Residual fungal material at each point in the decomposition sequence was analyzed using FTIR and thermochemolysis-GCMS with tetramethyl ammonium hydroxide. The recalcitrant fraction contained carbohydrate and amide-linked functional groups, which is consistent with the chitin or chitosan biopolymer. The breakdown of more labile organic carbon (including proteins and ester-linked groups) appears to occur on a more rapid time scale. Additionally, lipid biomarker analyses revealed a succession of microbial degraders in the degradation process. This is the first time a study of this kind has been performed using a widely distributed saprotrophic fungus, and indicates that these fungi are potentially important in long-term C

  3. Evolution of soil organic matter changes using pyrolysis and metabolic indices: a comparison between organic and mineral fertilization.

    PubMed

    Marinari, S; Masciandaro, G; Ceccanti, B; Grego, S

    2007-09-01

    The aim of this study was to evaluate chemical and biochemical changes of organic matter in fertilized (ammonium nitrate) and amended (vermicompost and manure) soils using pyrolysis and metabolic indices. The metabolic potential [dehydrogenase (DH-ase)/water soluble organic carbon (WSOC)], the metabolic quotient (qCO2) and the microbial quotient (Cmic:Corg) were calculated as indices of soil organic matter evolution. Pyrolysis-gas chromatography (Py-GC) was used to study structural changes in the organic matter. Carbon forms and microbial biomass have been measured by dichromate oxidation and fumigation-extraction methods, respectively. Dehydrogenase activity has been tested using INT (p-Iodonitrotetrazolium violet) as substrate. The results showed that organic amendment increased soil microbial biomass and its activity which were strictly related to pyrolytic mineralization and humification indices (N/O, B/E3). Mineral fertilization caused a greater alteration of native soil organic matter than the organic amendments, in that a high release of WSOC and relatively large amounts of aliphatic pyrolytic products, were observed. Therefore, the pyrolysis and metabolic indices provided similar and complementary information on soil organic matter changes after mineral and organic fertilization.

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

    NASA Astrophysics Data System (ADS)

    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

  5. Bioavailability of organic matter in a highly disturbed Estuary: The role of detrital and algal resources

    USGS Publications Warehouse

    Sobczak, W.V.; Cloern, J.E.; Jassby, A.D.; Muller-Solger, A. B.

    2002-01-01

    The importance of algal and detrital food supplies to the planktonic food web of a highly disturbed, estuarine ecosystem was evaluated in response to declining zooplankton and fish populations. We assessed organic matter bioavailability among a diversity of habitats and hydrologic inputs over 2 years in San Francisco Estuary's Sacramento-San Joaquin River Delta. Results show that bioavailable dissolved organic carbon from external riverine sources supports a large component of ecosystem metabolism. However, bioavailable particulate organic carbon derived primarily from internal phytoplankton production is the dominant food supply to the planktonic food web. The relative importance of phytoplankton as a food source is surprising because phytoplankton production is a small component of the ecosystem's organic-matter mass balance. Our results indicate that management plans aimed at modifying the supply of organic matter to riverine, estuarine, and coastal food webs need to incorporate the potentially wide nutritional range represented by different organic matter sources.

  6. Bioavailability of organic matter in a highly disturbed estuary: The role of detrital and algal resources

    PubMed Central

    Sobczak, William V.; Cloern, James E.; Jassby, Alan D.; Müller-Solger, Anke B.

    2002-01-01

    The importance of algal and detrital food supplies to the planktonic food web of a highly disturbed, estuarine ecosystem was evaluated in response to declining zooplankton and fish populations. We assessed organic matter bioavailability among a diversity of habitats and hydrologic inputs over 2 years in San Francisco Estuary's Sacramento–San Joaquin River Delta. Results show that bioavailable dissolved organic carbon from external riverine sources supports a large component of ecosystem metabolism. However, bioavailable particulate organic carbon derived primarily from internal phytoplankton production is the dominant food supply to the planktonic food web. The relative importance of phytoplankton as a food source is surprising because phytoplankton production is a small component of the ecosystem's organic-matter mass balance. Our results indicate that management plans aimed at modifying the supply of organic matter to riverine, estuarine, and coastal food webs need to incorporate the potentially wide nutritional range represented by different organic matter sources. PMID:12060756

  7. Effect of water saturation in soil organic matter on the partition of organic compounds

    USGS Publications Warehouse

    Rutherford, D.W.; Chlou, G.T.

    1992-01-01

    The sorption of benzene, trichloroethylene, and carbon tetrachloride at room temperature from water solution and from vapor on two high-organic-content soils (peat and muck) was determined in order to evaluate the effect of water saturation on the solute partition in soil organic matter (SOM). The uptake of water vapor was similarly determined to define the amounts of water in the saturated soil samples. In such high-organic-content soils the organic vapor sorption and the respective solute sorption from water exhibit linear isotherms over a wide range of relative concentrations. This observation, along with the low BET surface areas of the samples, suggests that partition in the SOM of the samples is the dominant process in the uptake of these liquids. A comparison of the sorption from water solution and from vapor phase shows that water saturation reduces the sorption (partition) efficiency of SOM by ?? 42%; the saturated water content is ??38% by weight of dry SOM. This reduction is relatively small when compared with the almost complete suppression by water of organic compound adsorption on soil minerals. While the effect of water saturation on solute uptake by SOM is much expected in terms of solute partition in SOM, the influence of water on the solubility behavior of polar SOM can be explained only qualitatively by regular solution theory. The results suggest that the major effect of water in a drying-wetting cycle on the organic compound uptake by normal low-organic-content soils (and the associated compound's activity) is the suppression of adsorption by minerals rather than the mitigation of the partition effect in SOM.

  8. Enzymatic Activity, Bacterial Distribution, and Organic Matter Composition in Sediments of the Ross Sea (Antarctica)

    PubMed Central

    Fabiano, Mauro; Danovaro, Roberto

    1998-01-01

    Enzymatic activities of aminopeptidase and β-glucosidase were investigated in Antarctic Ross Sea sediments at two sites (sites B and C, 567 and 439 m deep, respectively). The sites differed in trophic conditions related to organic matter (OM) composition and bacterial distribution. Carbohydrate concentrations at site B were about double those at site C, while protein and lipid levels were 10 times higher. Proteins were mainly found in a soluble fraction (>90%). Chloropigment content was generally low and phaeopigments were almost absent, indicating the presence of reduced inputs of primary organic matter. ATP concentrations (as a measure of the living microbial biomass) were significantly higher at site B. By contrast, benthic bacterial densities at site C were about double those at site B. Bacterial parameters do not appear to be “bottom-up controlled” by the amount of available food but rather “top-down controlled” by meiofauna predatory pressure, which was significantly higher at site B. Aminopeptidase and β-glucosidase extracellular enzyme activities (EEA) in Antarctic sediments appear to be high and comparable to those reported for temperate or Arctic sediments and characterized by low aminopeptidase/β-glucosidase ratios (about 10). Activity profiles showed decreasing patterns with increasing sediment depth, indicating vertical shifts in both availability and nutritional quality of degradable OM. Vertical profiles of aminopeptidase activity were related to a decrease in protein concentration and/or to an increase in the insoluble refractory proteinaceous fraction. The highest aminopeptidase activity rates were observed at site C, characterized by much lower protein concentrations. Differences in EEA between sites do not seem to be explained by differences in the in situ temperature (−1.6 and −0.8°C at sites B and C, respectively). Aminopeptidase activity profiles are consistent with the bacterial biomass and frequency of dividing cells. Enzyme

  9. Changes in the quality of chromophoric dissolved organic matter leached from senescent leaf litter during the early decomposition.

    PubMed

    Nishimura, Satoshi; Maie, Nagamitsu; Baba, Mitsuhisa; Sudo, Takahiro; Sugiura, Toshihiro; Shima, Eikichi

    2012-01-01

    Chromophoric dissolved organic matter (CDOM) leached from leaf litter is a major source of humus in mineral soil of forest ecosystems. While their functions and refractoriness depend on the physicochemical structure, there is little information on the quality of CDOM, especially for that leached in the very early stages of litter decomposition when a large amount of dissolved organic matter (DOM) is leached. This study aimed to better understand the variations/changes in the composition of CDOM leached from senescent leaf litter from two tree species during the early stage of decomposition. Leaf litter from a conifer tree (Japanese cedar, D. Don) and a deciduous broad-leaved tree (Konara oak, Thunb.) were incubated in columns using simulated rainfall events periodically for a total of 300 d at 20°C. The quality of CDOM was investigated based on the fluorescence properties by using a combination of excitation-emission matrix fluorescence (EEM) and parallel factor analysis (PARAFAC). In addition, the phenolic composition of DOM was investigated at a molecular level by thermally assisted hydrolysis and methylation-gas chromatography-mass spectrometry (THM-GC-MS) in the presence of tetramethylammonium hydroxide (TMAH). The EEM was statistically decomposed into eight fluorescence components (two tannin/peptide-like peaks, one protein-like peak, and five humic-like peaks). A significant contribution of tannin/peptide-like peaks was observed at the beginning of incubation, but these peaks decreased quickly and humic-like peaks increased within 1 mo of incubation. The composition of humic-like peaks was different between tree species and changed over the incubation period. Since tannin-derived phenolic compounds were detected in the DOM collected after 254 d of incubation on THM-GC-MS, it was suggested that tannins partially changed its structure, forming various humic-like peaks during the early decomposition.

  10. Simplified method to assess soil organic matter in landscape and carbon sequestration studies

    NASA Astrophysics Data System (ADS)

    Pallasser, Robert; Minasny, Budiman; McBratney, Alex; de Bruyn, Hank

    2010-05-01

    Soil organic matter (SOM) is composed of a variety of carbon bearing forms which are variably susceptible to degradation, itself a function of soil conditions (moisture, permeability, pH, Eh). Stability and residence time have become key questions relevant to soil carbon storage. Interestingly, organic matter types also differ in terms of their refractory stabilities making thermal analysis potentially an ideal way to resolve and analyse SOM. Elemental analyses of soils are routinely used to provide accurate total carbon determinations for the subsamples in question but cannot yield information about the relative amounts of labile to more stable carbon without involved chemical pre-treatment. Thermogravimetric analyses (TGA) have been commonly used to characterise chemical decomposition and to provide distinctive fingerprints (due to discrete mass changes) for mineral and organic materials. Such discrete changes in mass appear as peaks when registered on a DTGA (differential TGA) plot and correspond with dehydration, denaturing or oxidation events. Soil being a more complex continuum of organic and inorganic substances, many from fermentation reactions and microbial waste, does not have one particular fingerprint. Nonetheless, a number of relevant organic substances have characteristically different but consistent ignition temperatures (Lopez-Capel et. al., 2006; Laird et al., 2008; Xie et. al., 2009) allowing carbon pools to be distinguished thermally. In our studies, oxidative DTGA analyses of soils using a TA 2590 were typified by a bimodal distribution in SOM representing one less stable and one more stable group, a pattern similarly described by Siewert (2004). Current experiments indicate that the relative proportions of these SOM pulses are fairly reproducible but vary depending on soils and sampling depth (i.e. conditions) enabling it as a diagnostic parameter when considering SOM dynamics and humification. In order to compare this property numerically

  11. Mobilization of stable organic carbon in thawing permafrost by fresh organic matter from recent vegetation

    NASA Astrophysics Data System (ADS)

    Knoblauch, C.; Beer, C.; Pfeiffer, E. M.

    2015-12-01

    Permafrost affected soils contain 1,300 Pg organic carbon which is about twice the amount of the global vegetation. Most of this carbon (C) is locked in the perennially frozen ground (permafrost) and only a minor part is stored in the seasonal surface thaw layer (active layer). Rising arctic temperatures will cause deeper active layer thaw and permafrost degradation, which liberates additional soil organic matter (SOM) for microbial mineralization. After thaw, old permafrost C will be mixed with fresh organic matter from plant residues, e.g. by cryoturbation or leaching. Recent incubation studies have increased our understanding on how fast permafrost SOM may be mineralized to the greenhouse gases (GHG) carbon dioxide (CO2) and methane (CH4). After initial maximum GHG production from labile SOM components (labile C pool) mineralization rates slow down since the remaining SOM is more recalcitrant (stable C pool). The current study investigates if this stabile C pool may be mobilized by fresh organic matter from recent vegetation ("priming effect"). Therefore, permafrost samples (14C ages 0.1 - 17 ka BP) from the Siberian tundra were spiked with a 13C-labeled sedge (Carex aquatilis) after the samples were pre-incubated for 4 years. The amount of C released from permafrost SOM was calculated from the δ13C-values of produced GHG using a mixing model. Under aerobic conditions, all samples showed an accelerated mineralization of SOM after the addition of C. aquatilis (positive priming). After 4 months, which is about one vegetation period, the measured CO2 production exceeded the estimated CO2 release without labile plant material by 60 ± 28%. Under anaerobic conditions, priming was more pronounced increasing CO2 production by 100 ± 67% and CH4 production by 33 ± 32%. The CO2/CH4 ratio increased from 0.9 before priming to 1.3 after priming. The total mineralization of SOM over 4 months was significantly higher under aerobic (14.2 ± 6.1 μmol CO2-C gdw-1) than under

  12. Effect of organic matter on the sorption activity of heavy loamy soils for volatile organic compounds under low moisture conditions

    NASA Astrophysics Data System (ADS)

    Breus, I. P.; Mishchenko, A. A.; Shinkarev, A. A.; Neklyudov, S. A.; Breus, V. A.

    2014-12-01

    The diverse effect of the organic matter content on the sorption of vapors of aromatic and aliphatic hydrocarbons in soils under low moisture (<10.5%) has been revealed in sorption experiments using profile samples from two virgin heavy loamy dark gray forest soils characterized by relatively stable contents of finely dispersed mineral components. The decrease of the hydrocarbon sorption with increasing the content of organic matter under dry conditions (in the moisture range from 0 to 5-6%) indicates its lower sorption activity than that of the clay components and the blocking of the sorption sites on soil minerals by organic matter. At moisture contents above 5-6%, the effect of the soil composition on the sorption activity changes radically: it increases with increasing the content of organic matter. This is due to the inversion of the ratio between the activities of the soil components because of the hydrophilization of the surface of the mineral soil component. As a result, the sorption of water on the minerals reduces the mineral sorption activity to hydrocarbons to a lower level than the activity of organic matter. The maximum manifestation of the revealed blocking effect has been observed for the low-humus soils and this effect decreased with the accumulation of soil organic matter.

  13. Integrating Organic Matter Structure with Ecosystem Function using Advanced Analytical Chemistry Techniques

    NASA Astrophysics Data System (ADS)

    Boot, C. M.

    2012-12-01

    Microorganisms are the primary transformers of organic matter in terrestrial and aquatic ecosystems. The structure of organic matter controls its bioavailability and researchers have long sought to link the chemical characteristics of the organic matter pool to its lability. To date this effort has been primarily attempted using low resolution descriptive characteristics (e.g. organic matter content, carbon to nitrogen ratio, aromaticity, etc .). However, recent progress in linking these two important ecosystem components has been advanced using advanced high resolution tools (e.g. nuclear magnetic resonance (NMR) spectroscopy, and mass spectroscopy (MS)-based techniques). A series of experiments will be presented that highlight the application of high resolution techniques in a variety of terrestrial and aquatic ecosystems with the focus on how these data explicitly provide the foundation for integrating organic matter structure into our concept of ecosystem function. The talk will highlight results from a series of experiments including: an MS-based metabolomics and fluorescence excitation emission matrix approach evaluating seasonal and vegetation based changes in dissolved organic matter (DOM) composition from arctic soils; Fourier transform ion cyclotron resonance (FTICR) MS and MS metabolomics analysis of DOM from three lakes in an alpine watershed; and the transformation of 13C labeled glucose track with NMR during a rewetting experiment from Colorado grassland soils. These data will be synthesized to illustrate how the application of advanced analytical techniques provides novel insight into our understanding of organic matter processing in a wide range of ecosystems.

  14. Insight into dissolved organic matter fractions in Lake Wivenhoe during and after a major flood.

    PubMed

    Aryal, Rupak; Grinham, Alistair; Beecham, Simon

    2016-03-01

    Dissolved organic matter is an important component of biogeochemical processes in aquatic environments. Dissolved organic matter may consist of a myriad of different fractions and resultant processing pathways. In early January 2011, heavy rainfall occurred across South East Queensland, Australia causing significant catchment inflow into Lake Wivenhoe, which is the largest water supply reservoir for the city of Brisbane, Australia. The horizontal and vertical distributions of dissolved organic matter fractions in the lake during the flood period were investigated and then compared with stratified conditions with no catchment inflows. The results clearly demonstrate a large variation in dissolved organic matter fractions associated with inflow conditions compared with stratified conditions. During inflows, dissolved organic matter concentrations in the reservoir were fivefold lower than during stratified conditions. Within the dissolved organic matter fractions during inflow, the hydrophobic and humic acid fractions were almost half those recorded during the stratified period whilst low molecular weight neutrals were higher during the flood period compared to during the stratified period. Information on dissolved organic matter and the spatial and vertical variations in its constituents' concentrations across the lake can be very useful for catchment and lake management and for selecting appropriate water treatment processes.

  15. Insight into dissolved organic matter fractions in Lake Wivenhoe during and after a major flood.

    PubMed

    Aryal, Rupak; Grinham, Alistair; Beecham, Simon

    2016-03-01

    Dissolved organic matter is an important component of biogeochemical processes in aquatic environments. Dissolved organic matter may consist of a myriad of different fractions and resultant processing pathways. In early January 2011, heavy rainfall occurred across South East Queensland, Australia causing significant catchment inflow into Lake Wivenhoe, which is the largest water supply reservoir for the city of Brisbane, Australia. The horizontal and vertical distributions of dissolved organic matter fractions in the lake during the flood period were investigated and then compared with stratified conditions with no catchment inflows. The results clearly demonstrate a large variation in dissolved organic matter fractions associated with inflow conditions compared with stratified conditions. During inflows, dissolved organic matter concentrations in the reservoir were fivefold lower than during stratified conditions. Within the dissolved organic matter fractions during inflow, the hydrophobic and humic acid fractions were almost half those recorded during the stratified period whilst low molecular weight neutrals were higher during the flood period compared to during the stratified period. Information on dissolved organic matter and the spatial and vertical variations in its constituents' concentrations across the lake can be very useful for catchment and lake management and for selecting appropriate water treatment processes. PMID:26837382

  16. Organic matter and thermochemical sulfate reduction in the Viburnum Trend, southeast Missouri

    USGS Publications Warehouse

    Leventhal, J.S.

    1990-01-01

    The role of organic matter in Mississippi Valley-type Pb-Zn deposits has been studied by systematically sampling and characterizing various types of organic matter in the Upper Cambrian Bonneterre Formation in lead-zinc mines from the Viburnum Trend and from rocks as far as 20 km away from the Trend. Organic matter that is several kilometers from ore consists of insoluble disseminated kerogen in carbonates. Within meters to centimeters of ore in the Milliken mine, at the south end of the Viburnum Trend, organic matter occurs as solid, partly soluble tacky bitumen and insoluble hard blebs of millimeter to centimeter size. The solid insoluble organic matter in intimate contact (intergrown) with ore (galena and chalcopyrite) is friable and brittle. The sulfur content of solid organic matter from the Milliken mine varies and is lowest for tacky material away from ore, intermediate for blebs near ore, and highest for friable material in intimate contact with ore. Pyrolysis-gas chromatography of this sample suite documents the progression of kerogen (far from ore) through solid petroleumlike material (near ore) to degraded organic matter (in contact with ore). -from Author

  17. Organic matter quality of deep permafrost carbon - a study from Arctic Siberia

    NASA Astrophysics Data System (ADS)

    Strauss, J.; Schirrmeister, L.; Mangelsdorf, K.; Eichhorn, L.; Wetterich, S.; Herzschuh, U.

    2014-11-01

    The organic carbon (OC) pool accumulated in Arctic permafrost (perennially frozen ground) equals the carbon stored in the recent atmosphere. To give an idea of how Yedoma region permafrost could respond under future climatic warming, we conducted a study to quantify the organic matter quality for future decomposition of late Pleistocene (Yedoma) and Holocene (thermokarst) deposits on the Buor Khaya Peninsula, northeast Siberia. The objective of this study was to develop a stratigraphic classified organic matter quality characterization. For this purpose the degree of organic matter decomposition was estimated by using a multiproxy approach. We applied sedimentological (grain-size analyses, bulk density, ice content) and geochemical parameters (total OC, stable carbon isotopes (δ13C), carbon : nitrogen (C / N) ratios) as well as lipid biomarkers (n-alkanes, n-fatty acids, hopanes, triterpenoids, and biomarker proxies/indices: average chain length, carbon preference index (CPI), and higher plant fatty acid index (HPFA)). Our results show that the Yedoma and thermokarst organic matter qualities exhibit no obvious degradation - depth trend. The C / N, δ13C, and hop-17(21)-ene values and the HPFA index show a better quality of the organic matter stored in thermokarst deposits compared to Yedoma deposits, but the CPI points in the other direction. As the ranges of the proxies mostly overlap, we interpret this as to indicate similar quality for both kind of deposits with perhaps slightly better thermokarst organic matter quality. Supported by principal component analyses, the sediment parameters and quality proxies of Yedoma and thermokarst deposits could not be clearly separated from each other. This lack of clear quality differences revealed that the organic matter vulnerability is heterogeneous, independent from radiocarbon age and depends on different decomposition trajectories and the previous decomposition and preservation history. Elucidating this was one of the

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

    NASA Astrophysics Data System (ADS)

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

    2012-09-01

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

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

    USGS Publications Warehouse

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

    2012-01-01

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

  20. Sedimentary pigments on the Pakistan margin: Controlling factors and organic matter dynamics

    NASA Astrophysics Data System (ADS)

    Woulds, Clare; Cowie, Greg L.

    2009-03-01

    Sedimentary pigments can provide information on various aspects of benthic processes and biogeochemistry. In this study, sediments from sites at depths of 140 to 1850 m spanning the Pakistan margin oxygen minimum zone (OMZ), and representing dramatic contrasts in depositional conditions and benthic communities, were analysed for pigment yields and compositions. This has allowed a rare consideration of how different factors, including oxygen concentration, organic matter (OM) supply and biological activity (e.g., degree of bioturbation) may influence sedimentary pigment distribution in a continental margin environment. It has also allowed one of the first efforts to study the impact of biological activity on pigment concentrations in the natural environment, rather than in a microcosm setting. Total extractable surface sediment pigment concentrations showed a range of ˜1.5-49 μg g -1 of dry sediment. The pigment suite was dominated by pheophytin and pheophorbide (which together constituted ˜75% of total pigments), with minor amounts of chlorophyll- a, alloxanthin, diatoxanthin, zeaxanthin and β-carotene. Low oxygen concentration appeared to influence pigment abundance by increasing the concentration of refractory pigments ultimately buried. In addition, maximal pigment abundances were associated with minimal amounts of sediment mixing by macrofauna, and at one site macrofaunal digestion may have altered the relative dominance of the different pheopigments. In contrast, the lack of a marked increase in pigment concentrations after the summer monsoon plus the lack of a correlation between pigment concentration and water depth suggest that OM supply plays a relatively small role in controlling sedimentary pigments. Pigment concentrations and suites, together with modelled decay half-lives (˜0.8-15 years), suggest that in general OM on the Pakistan margin, despite the low oxygen concentrations and monsoon-driven productivity, is surprisingly degraded compared to

  1. PATTERNS AND CONTROLS OF DISSOLVED ORGANIC MATTER EXPORT BY MAJOR RIVERS: A NEW SEASONAL, SPATIALLY EXPLICIT, GLOBAL MODEL

    EPA Science Inventory

    River-derived dissolved organic matter (DOM) influences metabolism, light attenuation, and bioavailability of metals and nutrients in coastal ecosystems. Recent work suggests that DOM concentrations in surface waters vary seasonally because different organic matter pools are mobi...

  2. NITROGEN DEPOSITION AND ORGANIC MATTER MANIPULATIONS AFFECT GROSS AND NET NITROGEN TRANSFORMATIONS IN TWO TEMPERATE FORESTS SOILS

    EPA Science Inventory

    Soil nitrogen transformations are intricately linked to carbon transformations. We utilized two existing organic matter manipulation sites in western Oregon, USA and Hungary to investigate these linkages. Our questions were: 1) Does the quantity and quality of organic matter af...

  3. PHOTOREACTIVITY OF CHROMOPHORIC DISSOLVED ORGANIC MATTER (CDOM) DERIVED FROM DECOMPOSITION OF VARIOUS VASCULAR PLANT AND ALGAL SOURCES

    EPA Science Inventory

    Chromophoric dissolved organic matter (CDOM) in aquatic environments is derived from the microbial decomposition of terrestrial and microbial organic matter. Here we present results of studies of the spectral properties and photoreactivity of the CDOM derived from several organi...

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

    PubMed

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

    2013-06-01

    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. PMID:23466730

  5. Sustainable Water Supplies:Reducing The Organic Matter Content of Potable Water

    NASA Astrophysics Data System (ADS)

    Sohn, Mary

    2009-07-01

    As freshwater becomes a limiting factor in sustainable development, water treatment processes which can efficiently oxidize both anthropogenic and natural sources of organic matter are becoming crucial. While many anthropogenic organic compounds found in freshwater pose a direct risk to human health, natural organic matter such as humic acids, pose an indirect risk through the production of disinfection byproducts resulting from chlorination. Removal of dissolved natural organic matter before disinfection of potable water is recommended for the production of potable water in water treatment facilities. Several promising developments in dissolved organic matter oxidation are described including hydroxyl radical, advanced oxidation processes and ferrate (VI). The feasibility of applying these processes to water treatment on a large scale is largely dependent on cost.

  6. Role of bacteria in organic matter fluxes in the Southern California Coastal Zone: (Progress report)

    SciTech Connect

    Not Available

    1988-07-01

    The fate of organic matter in the sea, whether produced in situ or introduced from land, is greatly influenced by the metabolic trophic activities of the resident biota. Until recently it was thought that much of the primary production is consumed by the herbivores, making them the main determinants of fate of organic matter. It now appears that the microbial component of marine foodweb also plays a significant role in the decomposition, distribution, and vertical flux of organic material in seawater. The goal of the proposed research is to quantify this role of the microbial foodweb as part of a DOE-sponsored interdisciplinary study. We are testing the hypothesis that organic matter utilization by heterotrophic bacterioplankton represents a major sink for organic matter in the Southern California Coastal Zone.

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

    PubMed

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

    2013-06-01

    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.

  8. Catchment scale molecular composition of hydrologically mobilized dissolved organic matter

    NASA Astrophysics Data System (ADS)

    Raeke, Julia; Lechtenfeld, Oliver J.; Oosterwoud, Marieke R.; Bornmann, Katrin; Tittel, Jörg; Reemtsma, Thorsten

    2016-04-01

    Increasing concentrations of dissolved organic matter (DOM) in rivers of temperate catchments in Europe and North Amerika impose new technical challenges for drinking water production. The driving factors for this decadal increase in DOM concentration are not conclusive and changes in annual temperatures, precipitation and atmospheric deposition are intensely discussed. It is known that the majority of DOM is released by few but large hydrologic events, mobilizing DOM from riparian wetlands for export by rivers and streams. The mechanisms of this mobilization and the resulting molecular composition of the released DOM may be used to infer long-term changes in the biogeochemistry of the respective catchment. Event-based samples collected over two years from streams in three temperate catchments in the German mid-range mountains were analyzed after solid-phase extraction of DOM for their molecular composition by ultra-high resolution mass spectrometry (FT-ICR MS). Hydrologic conditions, land use and water chemistry parameters were used to complement the molecular analysis. The molecular composition of the riverine DOM was strongly dependent on the magnitude of the hydrologic events, with unsaturated, oxygen-enriched compounds being preferentially mobilized by large events. This pattern is consistent with an increase in dissolved iron and aluminum concentrations. In contrast, the relative proportions of nitrogen and sulfur bearing compounds increased with an increased agricultural land use but were less affected by the mobilization events. Co-precipitation experiments with colloidal aluminum showed that unsaturated and oxygen-rich compounds are preferentially removed from the dissolved phase. The precipitated compounds thus had similar chemical characteristics as compared to the mobilized DOM from heavy rain events. Radiocarbon analyses also indicated that this precipitated fraction of DOM was of comparably young radiocarbon age. DOM radiocarbon from field samples

  9. Pyrogenic and Fresh Organic Matter Effects on Soil Microbial Communities

    NASA Astrophysics Data System (ADS)

    Whitman, T.; Buckley, D. H.; Lehmann, J.

    2014-12-01

    Soils hold a globally important stock of carbon (C) and can act as both a C source and sink, depending on management and environmental conditions. Pyrogenic organic matter (PyOM) is produced naturally during fires, and contains relatively stable forms of C. Its intentional production has also been proposed as a mechanism for C management (in such cases PyOM is often referred to as "biochar"). However, the impact of natural or anthropogenic PyOM production on soils is complex and depends on many factors. In particular, PyOM additions to soils may have effects on plant growth and on native soil C cycling. The response of the soil microbial community to PyOM additions is likely key to understanding these interactions, but remains poorly characterized. We studied soil C dynamics and soil microbial communities in a field study with 350°C PyOM from 13C-labelled corn stover, a C3-derived soil, and C4 plants (sudangrass). PyOM additions only temporarily increased total soil CO2 fluxes, dramatically less than the increase associated with the addition of corn stover, which likely increased SOC losses. We used high-throughput sequencing of the 16S region on the MiSeq platform to characterize the initial, 12-day and 82-day soil bacterial communiities. We used three-part stable isotopic partitioning after two months to distinguish 334% higher root-derived CO2 fluxes in the plots with PyOM additions than those without, and 45% lower PyOM-C derived CO2 fluxes in the plots with plants present. The 84% increase in estimated cumulative soil CO2 emissions with stover additions was accompanied by a significant shift in the soil bacterial community on days 12 and 82, while the PyOM additions only resulted in significant changes to the overall community on day 82. We investigate which taxa are driving these community shifts, and how they may relate to the soil CO2 fluxes.

  10. Spatial distribution and transport of soil organic matter through a semi-arid catchment

    NASA Astrophysics Data System (ADS)

    Cammeraat, L. H.

    2009-04-01

    Soil erosion and deposition plays an important role in the transport and reallocation of organic matter in terrestrial carbon dynamics. This study discusses the production, transport and storage of organic material in semi-arid, semi-natural shrubland and forest ecosystem in SE Spain. Goal is to study the faith of organic matter in these land use systems and to reveal their possible importance within the terrestrial carbon cycle and the importance of the spatial redistribution of organic matter through the landscape. The study was carried out at the Alquería field station in the Guadalentín basin in SE Spain on calcareous soils. Measurements were carried out at plant, plot and (sub-) catchment scale incorporating Stipa tenacissima tussock dominated shrublands, Pinus halepensis open forests and almond and cereal fields. The determination of organic matter was based on the production and presence of organic matter on the soil surface, the amount of organic matter incorporated in the soil as present under and around individual plants and scaled up using high resolution aerial photographs and remote sensing images. The standing biomass was determined as well, using allometric methods and scaled up also using high resolution aerial photographs to estimate total plant cover. The transport of organic matter is determined using organic matter collected in classical unbounded plots that have been monitored also for runoff and sediment yield. Sediment stored in a 60 year old retention basin was also studied to reveal the sediment and organic matter fluxes at broader spatio-temporal scales. Furthermore also soil material accumulated behind bench terraces was evaluated for soil organic carbon. The results will be discussed in the context of the sources and sinks of organic matter as well as to their linkage to erosion and hydrological processes. The spatial heterogeneity of the accumulated and transported organic matter is strongly related to the frequency-magnitude of

  11. Defining organic matter quality in sediment systems: a suggested classification scheme

    NASA Astrophysics Data System (ADS)

    Alderson, Danielle; Evans, Martin; Rothwell, James; Boult, Stephen

    2015-04-01

    The quantity and quality of the mineral component of sediments is a core focus of sedimentological investigation in terrestrial systems. This is not to say that the organic component of collected sediments is simply ignored; the organic component is often scrutinised, but in some fields in a restricted manner, limited to basic characteristics such as the ratio of organic to mineral content derived from loss on ignition. There is no doubt that this information is useful; however, these types of analysis indicate the quantity of organic matter relative to a particular temporal scale or volume, rather than treating the organic fraction as a separate entity worthy of substantial investigation. The quality of the organic component is being increasingly considered in a number of fields, with molecular, thermal, spectroscopic and bulk methods being used. However, models and theories on organic matter processing in a variety of environmental systems, have been developed without clearly defining organic matter quality, because most results do not depend on an outright measure of quality (Bosatta and Agren, 1999). With approaches and techniques varying between fields, there is a need to consider a more systematic approach to the analysis and definition of organic matter quality. The disparities in the definition of the quality of organic matter, and thus how it may be measured have vital implications for the study of carbon cycling, biogeochemical processing, and ultimately ecosystem structure and function. The quality and quantity of organic matter have an influence on the chemistry and biology of systems and may reveal a wealth of past or contemporary environmental information. In this paper we provide a classification of organic matter quality and examples of potential applications and suitable techniques for the analysis of the main classes of organic matter character. A more consistent approach to organic matter characterisation has the potential to aid understanding of

  12. Contributions of organic and inorganic matter to sediment volume and accretion in tidal wetlands at steady state

    NASA Astrophysics Data System (ADS)

    Morris, James T.; Barber, Donald C.; Callaway, John C.; Chambers, Randy; Hagen, Scott C.; Hopkinson, Charles S.; Johnson, Beverly J.; Megonigal, Patrick; Neubauer, Scott C.; Troxler, Tiffany; Wigand, Cathleen

    2016-04-01

    A mixing model derived from first principles describes the bulk density (BD) of intertidal wetland sediments as a function of loss on ignition (LOI). The model assumes that the bulk volume of sediment equates to the sum of self-packing volumes of organic and mineral components or BD = 1/[LOI/k1 + (1-LOI)/k2], where k1 and k2 are the self-packing densities of the pure organic and inorganic components, respectively. The model explained 78% of the variability in total BD when fitted to 5075 measurements drawn from 33 wetlands distributed around the conterminous United States. The values of k1 and k2 were estimated to be 0.085 ± 0.0007 g cm-3 and 1.99 ± 0.028 g cm-3, respectively. Based on the fitted organic density (k1) and constrained by primary production, the model suggests that the maximum steady state accretion arising from the sequestration of refractory organic matter is ≤ 0.3 cm yr-1. Thus, tidal peatlands are unlikely to indefinitely survive a higher rate of sea-level rise in the absence of a significant source of mineral sediment. Application of k2 to a mineral sediment load typical of East and eastern Gulf Coast estuaries gives a vertical accretion rate from inorganic sediment of 0.2 cm yr-1. Total steady state accretion is the sum of the parts and therefore should not be greater than 0.5 cm yr-1 under the assumptions of the model. Accretion rates could deviate from this value depending on variation in plant productivity, root:shoot ratio, suspended sediment concentration, sediment-capture efficiency, and episodic events.

  13. Contributions of organic and inorganic matter to sediment volume and accretion in tidal wetlands at steady state

    PubMed Central

    Barber, Donald C.; Callaway, John C.; Chambers, Randy; Hagen, Scott C.; Hopkinson, Charles S.; Johnson, Beverly J.; Megonigal, Patrick; Neubauer, Scott C.; Troxler, Tiffany; Wigand, Cathleen

    2016-01-01

    Abstract A mixing model derived from first principles describes the bulk density (BD) of intertidal wetland sediments as a function of loss on ignition (LOI). The model assumes that the bulk volume of sediment equates to the sum of self‐packing volumes of organic and mineral components or BD = 1/[LOI/k1 + (1‐LOI)/k2], where k1 and k2 are the self‐packing densities of the pure organic and inorganic components, respectively. The model explained 78% of the variability in total BD when fitted to 5075 measurements drawn from 33 wetlands distributed around the conterminous United States. The values of k1 and k2 were estimated to be 0.085 ± 0.0007 g cm−3 and 1.99 ± 0.028 g cm−3, respectively. Based on the fitted organic density (k1) and constrained by primary production, the model suggests that the maximum steady state accretion arising from the sequestration of refractory organic matter is ≤ 0.3 cm yr−1. Thus, tidal peatlands are unlikely to indefinitely survive a higher rate of sea‐level rise in the absence of a significant source of mineral sediment. Application of k2 to a mineral sediment load typical of East and eastern Gulf Coast estuaries gives a vertical accretion rate from inorganic sediment of 0.2 cm yr−1. Total steady state accretion is the sum of the parts and therefore should not be greater than 0.5 cm yr−1 under the assumptions of the model. Accretion rates could deviate from this value depending on variation in plant productivity, root:shoot ratio, suspended sediment concentration, sediment‐capture efficiency, and episodic events.

  14. Refractory maintenance and repair

    SciTech Connect

    Biglin, J.

    1996-05-01

    Practical refractory application skills are developed most often through on-the-job experience. Many application decisions are judgment decisions carefully made after evaluating much information. Some decisions are made by trial-and-error--a trial is made on a small controlled area before a larger, permanent solution is implemented. Almost everyone involved in supplying and installing refractories will be called upon, at some time, to explain instances of poor refractory performance and service. The performance of refractories is influenced by: heat processing equipment design; refractory system design and type; operating practices; refractory and installation quality.

  15. Bioaugmentation with isolated strains for the removal of toxic and refractory organics from coking wastewater in a membrane bioreactor.

    PubMed

    Zhu, Xiaobiao; Liu, Rui; Liu, Cong; Chen, Lujun

    2015-11-01

    The bioaugmentation strains for phenol, pyridine, quinoline, carbazole, and naphthalene degradation were employed to treat coking wastewater in a membrane bioreactor (MBR). The results showed that the bioaugmented MBR was much better in pollutant removal than that of the control MBR with conventional activated sludge. Compared to the control MBR, the bioaugmented MBR displayed an additional 3.2 mg/L of phenol, pyridine, quinoline, naphthalene and carbazole in total by the addition of the degrading strains. Also, about 10 % of the chemical oxygen demand in the effluent was further removed by the bioaugmentation. The pyrosequencing analysis of the sludge in the MBRs revealed that the microbial community shifted in response to the addition of the degrading strains. The diversity of the microbial community increased during the bioaugmentation, and some bacterial taxa favorable to the removal of toxic and refractory pollutants appeared in the bioaugmented MBR. The results indicated that the use of high-efficiency bacteria was a feasible method for industrial coking wastewater treatment. PMID:26510738

  16. Efficacy and Safety of Intravenous Immunoglobulin Treatment in Refractory Behcet's Disease with Different Organ Involvement: A Case Series.

    PubMed

    Cantarini, Luca; Stromillo, Maria L; Vitale, Antonio; Lopalco, Giuseppe; Emmi, Giacomo; Silvestri, Elena; Federico, Antonio; Galeazzi, Mauro; Iannone, Florenzo; De Stefano, Nicola

    2016-01-01

    Behçet's disease (BD) is a multi-systemic disorder of unknown etiology characterized by relapsing oral-genital ulcers, uveitis, and involvement of the articular, gastrointestinal, neurologic, and vascular systems. The choice of treatment is based on the severity of systemic involvement, clinical presentation and the site affected, and includes corticosteroids, azathioprine, interferon, cyclophosphamide, methotrexate or tumor necrosis factor-alpha and interleukin-1 blockers. We present a case series of four refractory BD patients successfully treated with intravenous immunoglobulins (IVIG). All patients fulfilled International Study Group criteria. The patients' mean age was 38.75 ± 12.09 years and mean disease duration 10.25 ± 8.5 years. Human leukocyte antigen B51 was positive in two of four patients. In addition to oral aphthosis, all patients suffered from genital ulcers and cutaneous BD-related manifestations; central nervous system involvement and arthralgia were found in two patients. Peripheral nervous system, gastrointestinal and eye involvement occurred in 25% of cases. In all patients, previously treated according to EULAR recommendations without reaching satisfactory results, IVIG induced immediate and sustained response over time without incurring any side effects. We propose IVIG administration as an additional effective and safe treatment option in patients with severe and resistant BD. PMID:27228652

  17. High-molecular-weight organic matter in the particles of comet 67P/Churyumov–Gerasimenko

    NASA Astrophysics Data System (ADS)

    Fray, Nicolas; Bardyn, Anaïs; Cottin, Hervé; Altwegg, Kathrin; Baklouti, Donia; Briois, Christelle; Colangeli, Luigi; Engrand, Cécile; Fischer, Henning; Glasmachers, Albrecht; Grün, Eberhard; Haerendel, Gerhard; Henkel, Hartmut; Höfner, Herwig; Hornung, Klaus; Jessberger, Elmar K.; Koch, Andreas; Krüger, Harald; Langevin, Yves; Lehto, Harry; Lehto, Kirsi; Le Roy, Léna; Merouane, Sihane; Modica, Paola; Orthous-Daunay, François-Régis; Paquette, John; Raulin, François; Rynö, Jouni; Schulz, Rita; Silén, Johan; Siljeström, Sandra; Steiger, Wolfgang; Stenzel, Oliver; Stephan, Thomas; Thirkell, Laurent; Thomas, Roger; Torkar, Klaus; Varmuza, Kurt; Wanczek, Karl-Peter; Zaprudin, Boris; Kissel, Jochen; Hilchenbach, Martin

    2016-10-01

    The presence of solid carbonaceous matter in cometary dust was established by the detection of elements such as carbon, hydrogen, oxygen and nitrogen in particles from comet 1P/Halley. Such matter is generally thought to have originated in the interstellar medium, but it might have formed in the solar nebula—the cloud of gas and dust that was left over after the Sun formed. This solid carbonaceous material cannot be observed from Earth, so it has eluded unambiguous characterization. Many gaseous organic molecules, however, have been observed; they come mostly from the sublimation of ices at the surface or in the subsurface of cometary nuclei. These ices could have been formed from material inherited from the interstellar medium that suffered little processing in the solar nebula. Here we report the in situ detection of solid organic matter in the dust particles emitted by comet 67P/Churyumov–Gerasimenko the carbon in this organic material is bound in very large macromolecular compounds, analogous to the insoluble organic matter found in the carbonaceous chondrite meteorites. The organic matter in meteorites might have formed in the interstellar medium and/or the solar nebula, but was almost certainly modified in the meteorites’ parent bodies. We conclude that the observed cometary carbonaceous solid matter could have the same origin as the meteoritic insoluble organic matter, but suffered less modification before and/or after being incorporated into the comet.

  18. Effects of dissolved organic matter on toxicity and bioavailability of copper for lettuce sprouts.

    PubMed

    Inaba, Shoko; Takenaka, Chisato

    2005-05-01

    It is well known that dissolved organic matter in soil solution may affect the toxicity or bioavailability of heavy metals to plants, but existing information on various organic substances is insufficient for treating problems with heavy metal-contaminated soils. To clarify how dissolved organic matter alters the toxicity and bioavailability of metals, we germinated lettuce seeds exposed to solutions containing Cu and several kinds of dissolved organic matters. Low molecular weight organic acids (citric, malic, and oxalic acids) increased the toxicity and bioavailability of Cu, but low concentrations of the synthetic chelators ethylenediamine tetra-acetic acid (EDTA) and diethylenetriamine penta-acetic acid (DTPA) decreased the toxicity and bioavailability of Cu. In contrast, humic acid appeared to be the most effective organic substance for detoxifying Cu, even though it did not significantly decrease the bioavailability of Cu. Consequently, the bioavailability and toxic effects of Cu in soil depend on the nature of coexisting organic substances in the soil solution.

  19. Depletion of 13C in Cretaceous marine organic matter: Source, diagenetic, or environmental sigal?

    USGS Publications Warehouse

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

    1986-01-01

    Geochemical studies of Cretaceous strata rich in organic carbon (OC) from Deep Sea Drilling Project (DSDP) sites and several land sections reveal several consistent relationships among amount of OC, hydrocarbon generating potential of kerogen (measured by pyrolysis as the hydrogen index, HI), and the isotopic composition of the OC. First, there is a positive correlation between HI and OC in strata that contain more than about 1% OC. Second, percent OC and HI often are negatively correlated with carbon isotopic composition (?? 13C) of kerogen. The relationship between HI and OC indicates that as the amount of organic matter increases, this organic matter tends to be more lipid rich reflecting the marine source of the organic matter. Cretaceous samples that contain predominantly marine organic matter tend to be isotopically lighter than those that contain predominantly terrestrial organic matter. Average ?? 13C values for organic matter from most Cretaceous sites are between -26 and -28???, and values heavier than about -25??? occur at very few sites. Most of the ?? 13C values of Miocene to Holocene OC-rich strata and modern marine plankton are between -16 to -23???. Values of ??13C of modern terrestrial organic matter are mostly between -23 and -33???. The depletion of terrestial OC in 13C relative to marine planktonic OC is the basis for numerous statements in the literature that isotopically light Cretaceous organic matter is of terrestrial origin, even though other organic geochemical and(or) optical indicators show that the organic matter is mainly of marine origin. A difference of about 5??? in ?? 13C between modern and Cretaceous OC-rich marine strata suggests either that Cretaceous marine planktonic organic matter had the same isotopic signature as modern marine plankton and that signature has been changed by diagenesis, or that OC derived from Cretaceous marine plankton was isotopically lighter by about 5??? relative to modern plankton OC. Diagenesis does

  20. Solid Phase Peat and Dissolved Organic Matter Composition and Reactivity as a Function of Surface Vegetation in Northern Minnesota Peatlands

    NASA Astrophysics Data System (ADS)

    Tfaily, M. M.; Hamdan, R.; Jaffe, R.; Cawley, K.; Cooper, W. T.; Chanton, J.

    2012-12-01

    Peatlands are unusual in greenhouse scenarios because on the one hand they sequester carbon from the atmosphere as peat, while on the other hand they re-emit it in large quantities as methane. Little is known, however, about the chemical processes that link solid phase peat and dissolved organic matter (DOM) within its porewaters. In this work we have applied FT-IR and 13C NMR spectroscopy to characterize the solid phase peat at varying depths from different sites at the Marcell Experimental Forest (MEF) where the Oak Ridge National Laboratory (ORNL) has begun the Spruce and Peatland Response Under Climatic and Environmental Change (SPRUCE) project. Parallel Factor analyzed Excitation/Emission Matrix fluorescence spectroscopy (PARAFAC-EEMS) and ultrahigh resolution Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (FT-ICR-MS) were used to characterize the molecular composition of peat porewaters. Analyses of the solid phase and the porewater suggested the presence of different zones of varying degrees of humification in the peat core. FT-IR and NMR data indicated that the relative abundances of alipahtics and aromatics increased with depth to about 100 cm, then remained relatively constant. This increase was accompanied with a concomitant decrease in the relative abundance of carbohydrates. FT-ICR MS data showed a large abundance of compounds with high O/C ratios at the surface (acrotelm) that tend to disappear with depth (catotelm), with accumulation of refractory aliphatic compounds characterized by low O/C and high H/C ratios.

  1. Enhanced binding of hydrophobic organic contaminants by microwave-assisted humification of soil organic matter.

    PubMed

    Hur, Jin; Park, Sung-Won; Kim, Min Chan; Kim, Han S

    2013-11-01

    Enhanced binding of hydrophobic organic contaminants (HOCs) with soil organic matter (SOM) by microwave (MW) irradiation was investigated in this study. We used fluorescence excitation emission matrix, humification index (HIX), and organic carbon partitioning coefficient (Koc) to examine characteristic changes in SOM and its sorptive capacity for HOCs. When MW was irradiated to soils, protein-like fluorescence decreased but fulvic- and humic-like fluorescence increased. The addition of activated carbon in the presence of oxygen facilitated the humification-like alteration of SOM more significantly, evidenced by increases in fulvic- and humic-like fluorescence signals. The extent of SOM-phenanthrene binding also increased with MW treatment, supported by a notable increase in Koc value from 1.8×10(4) to 7.3×10(5)Lkg(-1). Various descriptors indicating the physical and chemical properties of SOM along with the relative percentage of humic-like fluorescence and HIX values demonstrated strong linear relationships with Koc values. These linear relationships indicated that the increased binding affinity of SOM for phenanthrene was attributed to enhanced SOM humification, which was stimulated by MW irradiation. Thus, our results demonstrate that MW irradiation could be effectively used for remediation or for assessing the environmental risks of HOC-contaminated soils and groundwater.

  2. Effects of polar and nonpolar groups on the solubility of organic compounds in soil organic matter

    USGS Publications Warehouse

    Chiou, C.T.; Kile, D.E.

    1994-01-01

    Vapor sorption capacities on a high-organic-content peat, a model for soil organic matter (SOM), were determined at room temperature for the following liquids: n-hexane, 1,4-dioxane, nitroethane, acetone, acetonitrile, 1-propanol, ethanol, and methanol. The linear organic vapor sorption is in keeping with the dominance of vapor partition in peat SOM. These data and similar results of carbon tetrachloride (CT), trichloroethylene (TCE), benzene, ethylene glycol monoethyl ether (EGME), and water on the same peat from earlier studies are used to evaluate the effect of polarity on the vapor partition in SOM. The extrapolated liquid solubility from the vapor isotherm increases sharply from 3-6 wt % for low-polarity liquids (hexane, CT, and benzene) to 62 wt % for polar methanol and correlates positively with the liquid's component solubility parameters for polar interaction (??P) and hydrogen bonding (??h). The same polarity effect may be expected to influence the relative solubilities of a variety of contaminants in SOM and, therefore, the relative deviations between the SOM-water partition coefficients (Kom) and corresponding octanol-water partition coefficients (Kow) for different classes of compounds. The large solubility disparity in SOM between polar and nonpolar solutes suggests that the accurate prediction of Kom from Kow or Sw (solute water solubility) would be limited to compounds of similar polarity.

  3. Investigation of the organic matter in inactive nuclear tank liquids. Environmental Restoration Program

    SciTech Connect

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

    1990-08-01

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

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

    NASA Astrophysics Data System (ADS)

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

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

  5. Bacteria-organic matter coupling and its significance for oceanic carbon cycling.

    PubMed

    Azam, F; Smith, D C; Steward, G F; Hagström, A

    1994-09-01

    This paper synthesizes current ideas on the role of the microbial loop in carbon fluxes in the ocean and proposes some directions for future research. Organic matter flux into bacteria is highly variable, which can significantly influence the pathways of carbon flow in the ocean. A goal for future research is to elucidate the mechanistic bases of bacteria-organic matter coupling. This research should take into consideration the micrometer-scale distribution of bacteria and the composition, structure, and dynamics of the organic matter field in the bacterium's microhabitat. The ideas on the interactions of bacteria with the particulate organic phase need to be revised in view of recent findings of highly abundant, previously unknown particles ranging in size from nanometers to hundreds of micrometers. The "hot-spots" in the distribution of organic matter and remineralized nutrients can influence the rates as well as the direction of biogeochemical fluxes. Slow-to-degrade dissolved organic matter (DOM) may be produced because of loose bacteria-organic matter coupling resulting in DOM storage. Its use at a later time and place has profound implications for carbon fluxes and food web dynamics. A fundamental research need for the future is to understand the ecological interactions among the members of the microbial loop in an appropriate microhabitat context. While this goal was previously intractable, new molecular and optical techniques should make it possible to understand the biogeochemical activities of the microbial loop in terms of the ecology and evolution of pelagic microbial communities.

  6. Sources and Fates of Dissolved Organic Matter in the Mid-Atlantic Bight

    SciTech Connect

    Hopkinson, C. S.

    2000-08-16

    The objectives of the research program were to identify and determine the relative importance of various sources of dissolved organic matter to the continental shelf, and to estimate the net carbon balance for the Middle Atlantic Bight.

  7. Northern Gulf of Mexico estuarine coloured dissolved organic matter derived from MODIS data

    EPA Science Inventory

    Coloured dissolved organic matter (CDOM) is relevant for water quality management and may become an important measure to complement future water quality assessment programmes. An approach to derive CDOM using the Moderate Resolution Imaging Spectroradiometer (MODIS) was developed...

  8. Photobleaching Kinetics of Chromophoric Dissolved Organic Matter Derived from Mangrove Leaf Litter and Floating Sargassum Colonies

    EPA Science Inventory

    We examined the photoreactivity of chromophoric dissolved organic matter (CDOM) derived from Rhizophora mangle (red mangrove) leaf litter and floating Sargassum colonies as these marine plants can be important contributors to coastal and open ocean CDOM pools, respectively. Mangr...

  9. THE ROLE OF NITROGEN IN CHROMOPHORIC AND FLUORESCENT DISSOLVED ORGANIC MATTER FORMATION

    EPA Science Inventory

    Microbial and photochemical processes affect chromophoric dissolved organic matter (CDOM) dynamics in the ocean. Some evidence suggests that dissolved nitrogen plays a role in CDOM formation, although this has received little systematic attention in marine ecosystems. Coastal sea...

  10. CHROMOPHORIC DISSOLVED ORGANIC MATTER (CDOM) SOURCE CHARACTERIZATION IN THE LOUISIANA BIGHT

    EPA Science Inventory

    Chromophoric dissolved organic matter (CDOM) in the Mississippi plume region may have several distinct sources: riverine (terrestrial soils), wetland (terrestrial plants), biological production (phytoplankton, zooplankton, microbial), and sediments. Complex mixing, photodegradati...

  11. Lyophilization, Reconstitution, and DBP Formation in Reverse-Osmosis Concentrated Natural Organic Matter

    EPA Science Inventory

    Drinking water treatment and disinfection byproduct (DBP) research can be complicated by natural organic matter (NOM) temporal variability. NOM preservation by lyophilization (freeze-drying) has been long practiced to address this issue; however, its applicability for drinking w...

  12. REFERENCE MATERIALS AND QUALITY ASSURANCE FOR THE CHARACTERIZATION OF ORGANIC COMPOUNDS IN PARTICULATE MATTER

    EPA Science Inventory

    One of the first environmental matrix Standard Reference Materials (SRMs) developed by the National Institute of Standards and Technology (NIST) for determination of organic species was SRM 1649 Urban Dust, ambient total suspended particulate matter (PM) collected in Washington D...

  13. Natural organic matter (NOM) in a limed lake and its tributaries.

    PubMed

    Andersen, Dag O; Gjessing, Egil T

    2002-05-01

    The chemistry of a limed lake and its main tributaries were studied for 3 years (1992-94) with an emphasis on natural organic matter (NOM). Increased transparency and decreased water colour indicated a general reduction of NOM in the lake. Increased A(254 nm)/A(410 nm) ratios in the epilimnion during summer and early autumn suggested degradation of higher molecular size organic matter into low molecular size NOM. Increase in ammonium and dissolved inorganic carbon concentrations in the lake was possibly due to the NOM degradation. Using budget calculations and the literature values, photodegradation and microbial activity were estimated to be the main mechanisms of the NOM removal. These mechanisms accounted for about 30-35% and 60-65% of the total loss of organic matter, respectively, in the summer and early autumn period. Low sedimentation rates indicate that co-precipitation of organic matter with calcium, aluminium and/or iron was of minor importance in these seasons.