Degradation of surface-water dissolved organic matter: influences of DOM chemical characteristics and microbial populations

Hydrobiologia ◽  
2005 ◽  
Vol 539 (1) ◽  
pp. 1-11 ◽  
Author(s):  
Katherine C. Young ◽  
Kathryn M. Docherty ◽  
Patricia A. Maurice ◽  
Scott D. Bridgham
Keyword(s):  
Organic Matter ◽  
Surface Water ◽  
Dissolved Organic Matter ◽  
Microbial Populations ◽  
Chemical Characteristics

Removal of the Neutral Dissolved Organic Matter (NDOM) from Surface Water by Coagulation/Flocculation and Nanofiltration

2021 ◽  
pp. 1-14
Author(s):  
Sami Khettaf ◽  
Roumaissa Boumaraf ◽  
Fatiha Benmahdi ◽  
Kamel-Eddine Bouhidel ◽  
Mohammed Bouhelassa
Keyword(s):  
Organic Matter ◽  
Surface Water ◽  
Dissolved Organic Matter

scholarly journals Compositional and chemical characteristics of dissolved organic matter in various types of cropped and natural Chinese soils

2019 ◽  
Vol 6 (1) ◽  
Author(s):  
Songyan Li ◽  
Meng Li ◽  
Guoxi Wang ◽  
Xiaolei Sun ◽  
Beidou Xi ◽  
...  
Keyword(s):  
Organic Matter ◽  
Dissolved Organic Matter ◽  
Soil Type ◽  
Spectral Characteristics ◽  
Terrestrial Ecosystems ◽  
Soil Types ◽  
Chemical Characteristics ◽  
Natural Soils ◽  
Red Soils ◽  
Chernozem Soils

Abstract Background Exploration of composition and chemical characteristics of soil dissolved organic matter (DOM) is significant to understand its biogeochemical role in terrestrial ecosystems. A total of 43 cropped and 16 natural soils (0–20 cm) under four soil types (cinnamon, chernozem, red and paddy soils) across China were collected to investigate the spectral characteristics of DOM using UV–Vis and 3D-EEM spectroscopy. Results The chernozem soils exhibited the highest aromaticity and humification degree among the four soil types. Ranges of biological index (BIX, 0.53–1.17) and fluorescence index (FI, 1.55–2.10) were found in the investigated DOM, showing joint contribution from allochthonous and autochthonous sources. Higher BIX and FI in the DOM of the paddy and red soils indicated a greater reliance on autochthonous sources for these two soil types. The cropped soils showed no significant differences in chemical characteristics and sources from the natural soils for the cinnamon, chernozem and red soils. UVA (16.2–47.9%) and UVC fulvic-like substances (15.4–40.5%) were the prevailing DOM components, which were highest in the chernozem soils. Additionally, the cropped soils had a higher proportion of humic-like substances than the natural soils in the DOM. Conclusions Both soil type and land-use strongly affected the chemical characteristics of soil DOM, but only soil type had an impact on the DOM composition for the collected soils. These findings may contribute to the prediction of the biochemical behavior of soil DOM under different soil types and land-uses in terrestrial ecosystems.

scholarly journals Photomineralization and photomethanification of dissolved organic matter in Saguenay River surface water

2015 ◽  
Vol 12 (22) ◽  
pp. 6823-6836 ◽  
Author(s):  
Y. Zhang ◽  
H. Xie
Keyword(s):  
Organic Matter ◽  
Surface Water ◽  
Dissolved Organic Matter ◽  
Dimethyl Sulfide ◽  
Ultraviolet B ◽  
Global Ocean ◽  
Quantum Yields ◽  
Methyl Radical ◽  
Ch4 Production ◽  
Saguenay River

Abstract. Rates and apparent quantum yields of photomineralization (AQYDOC) and photomethanification (AQYCH4) of chromophoric dissolved organic matter (CDOM) in Saguenay River surface water were determined at three widely differing dissolved oxygen concentrations ([O2]) (suboxic, air saturation, and oxygenated) using simulated-solar radiation. Photomineralization increased linearly with CDOM absorbance photobleaching for all three O2 treatments. Whereas the rate of photochemical dissolved organic carbon (DOC) loss increased with increasing [O2], the ratio of fractional DOC loss to fractional absorbance loss showed an inverse trend. CDOM photodegradation led to a higher degree of mineralization under suboxic conditions than under oxic conditions. AQYDOC determined under oxygenated, suboxic, and air-saturated conditions increased, decreased, and remained largely constant with photobleaching, respectively; AQYDOC obtained under air saturation with short-term irradiations could thus be applied to longer exposures. AQYDOC decreased successively from ultraviolet B (UVB) to ultraviolet A (UVA) to visible (VIS), which, alongside the solar irradiance spectrum, points to VIS and UVA being the primary drivers for photomineralization in the water column. The photomineralization rate in the Saguenay River was estimated to be 2.31 × 108 mol C yr−1, accounting for only 1 % of the annual DOC input into this system. Photoproduction of CH4 occurred under both suboxic and oxic conditions and increased with decreasing [O2], with the rate under suboxic conditions ~ 7–8 times that under oxic conditions. Photoproduction of CH4 under oxic conditions increased linearly with photomineralization and photobleaching. Under air saturation, 0.00057 % of the photochemical DOC loss was diverted to CH4, giving a photochemical CH4 production rate of 4.36 × 10−6 mol m−2 yr−1 in the Saguenay River and, by extrapolation, of (1.9–8.1) × 108 mol yr−1 in the global ocean. AQYCH4 changed little with photobleaching under air saturation but increased exponentially under suboxic conditions. Spectrally, AQYCH4 decreased sequentially from UVB to UVA to VIS, with UVB being more efficient under suboxic conditions than under oxic conditions. On a depth-integrated basis, VIS prevailed over UVB in controlling CH4 photoproduction under air saturation while the opposite held true under O2-deficiency. An addition of micromolar levels of dissolved dimethyl sulfide (DMS) substantially increased CH4 photoproduction, particularly under O2-deficiency; DMS at nanomolar ambient concentrations in surface oceans is, however, unlikely a significant CH4 precursor. Results from this study suggest that CDOM-based CH4 photoproduction only marginally contributes to the CH4 supersaturation in modern surface oceans and to both the modern and Archean atmospheric CH4 budgets, but that the photochemical term can be comparable to microbial CH4 oxidation in modern oxic oceans. Our results also suggest that anoxic microniches in particulate organic matter and phytoplankton cells containing elevated concentrations of precursors of the methyl radical such as DMS may provide potential hotspots for CH4 photoproduction.

scholarly journals Surface water treatment by UV/H2O2 with subsequent soil aquifer treatment: impact on micropollutants, dissolved organic matter and biological activity

2019 ◽  
Vol 5 (10) ◽  
pp. 1709-1722 ◽  
Author(s):  
Robin Wünsch ◽  
Julia Plattner ◽  
David Cayon ◽  
Fabienne Eugster ◽  
Jens Gebhardt ◽  
...  
Keyword(s):  
Organic Matter ◽  
Biological Activity ◽  
Water Treatment ◽  
Surface Water ◽  
Dissolved Organic Matter ◽  
Microbial Activity ◽  
Soil Aquifer Treatment ◽  
Organic Micropollutants ◽  
Total Removal ◽  
Surface Water Treatment

UV/H2O2 treatment of sand-filtered surface water before soil aquifer treatment increases the total removal of organic micropollutants and has an impact on microbial activity without pronounced effects on dissolved organic matter removal.

scholarly journals Photomineralization and photomethanification of dissolved organic matter in Saguenay River surface water

2015 ◽  
Vol 12 (16) ◽  
pp. 14303-14341 ◽  
Author(s):  
Y. Zhang ◽  
H. Xie
Keyword(s):  
Organic Matter ◽  
Surface Water ◽  
Dissolved Organic Matter ◽  
Dimethyl Sulfide ◽  
Ultraviolet B ◽  
Global Ocean ◽  
Quantum Yields ◽  
Methyl Radical ◽  
Ch4 Production ◽  
Saguenay River

Abstract. Rates and apparent quantum yields of photomineralization (AQYDOC) and photomethanification (AQYCH4) of chromophoric dissolved organic matter (CDOM) in Saguenay River surface water were determined at three widely differing dissolved oxygen concentrations ([O2]) (suboxic, air-saturation, and oxygenated) using simulated-solar radiation. Photomineralization increased linearly with CDOM absorbance photobleaching for all three O2 treatments. Whereas the rate of photochemical dissolved organic carbon (DOC) loss increased with increasing [O2], the ratio of fractional DOC loss to fractional absorbance loss showed an inverse trend. CDOM photodegradation led to a nearly complete mineralization under suboxic conditions but to only a partial mineralization under oxic conditions. AQYDOC determined under oxygenated, suboxic, and air-saturated conditions increased, decreased, and remained largely constant with photobleaching, respectively; AQYDOC obtained under air-saturation with short-term irradiations could thus be applied to longer exposures. AQYDOC decreased successively from ultraviolet B (UVB) to ultraviolet A (UVA) to visible (VIS), which, alongside the solar irradiance spectrum, points to VIS and UVA being the primary drivers for photomineralization in the water column. The photomineralization rate in the Saguenay River was estimated to be 2.31 × 108 mol C yr−1, accounting for only 1 % of the annual DOC input into this system. Photoproduction of CH4 occurred under both suboxic and oxic conditions and increased with decreasing [O2], with the rate under suboxic conditions ~ 7–8 times that under oxic conditions. Photoproduction of CH4 under oxic conditions increased linearly with photomineralization and photobleaching. Under air-saturation, 0.00057 % of the photochemical DOC loss was diverted to CH4, giving a photochemical CH4 production rate of 4.36 × 10−6 mol m−2 yr−1 in the Saguenay River and, by extrapolation, of (1.9–8.1) × 108 mol yr−1 in the global ocean. AQYCH4 changed little with photobleaching under air-saturation but increased exponentially under suboxic conditions. Spectrally, AQYCH4 decreased sequentially from UVB to UVA to VIS, with UVB being more efficient under suboxic conditions than under oxic conditions. On a depth-integrated basis, VIS prevailed over UVB in controlling CH4 photoproduction under air-saturation while the opposite held true under O2-deficiency. An addition of micromolar levels of dissolved dimethyl sulfide (DMS) substantially increased CH4 photoproduction, particularly under O2-deficiency; DMS at nanomolar ambient concentrations in surface oceans is, however, unlikely a significant CH4 precursor. Results from this study suggest that CDOM-based CH4 photoproduction only marginally contributes to the CH4 supersaturation in modern surface oceans and to both the modern and Archean atmospheric CH4 budgets, but that the photochemical term can be comparable to microbial CH4 oxidation in modern oxic oceans. Our results also suggest that anoxic microniches in particulate organic matter and phytoplankton cells containing elevated concentrations of precursors of the methyl radical such as DMS may provide potential hotspots for CH4 photoproduction.

scholarly journals Protein analysis in dissolved organic matter: What proteins from organic debris, soil leachate and surface water can tell us - a perspective

2005 ◽  
Vol 2 (1) ◽  
pp. 75-86 ◽  
Author(s):  
W. X. Schulze
Keyword(s):  
Organic Matter ◽  
Surface Water ◽  
Dissolved Organic Matter ◽  
Protein Analysis ◽  
Mass Spectrometric ◽  
Environmental Research ◽  
Model Organisms ◽  
Water Current ◽  
Soil Leachate ◽  
Protein Pool

Abstract. Mass spectrometry based analysis of proteins is widely used to study cellular processes in model organisms. However, it has not yet routinely been applied in environmental research. Based on observations that protein can readily be detected as a component of dissolved organic matter (DOM), this article gives an example about the possible use of protein analysis in ecology and environmental sciences focusing on different terrestrial ecosystems. At this stage, there are two areas of interest: (1) the identification of phylogenetic groups contributing to the environmental protein pool, and (2) identification of the organismic origin of specific enzymes that are important for ecosystem processes. In this paper, mass spectrometric protein analysis was applied to identify proteins from decomposing plant material and DOM of soil leachates and surface water samples derived from different environments. It is concluded, that mass spectrometric protein analysis is capable of distinguishing phylogenetic origin of proteins from litter protein extracts, leachates of different soil horizons, and from various sources of terrestrial surface water. Current limitation is imposed by the limited knowledge of complete genomes of soil organisms. The protein analysis allows to relate protein presence to biogeochemical processes, and to identify the source organisms for specific active enzymes. Further applications, such as in pollution research are conceivable. In summary, the analysis of proteins opens a new area of research between the fields of microbiology and biogeochemistry.

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