scholarly journals The One-Sample PARAFAC Approach Reveals Molecular Size Distributions of Fluorescent Components in Dissolved Organic Matter

2017 ◽  
Vol 51 (20) ◽  
pp. 11900-11908 ◽  
Author(s):  
Urban J. Wünsch ◽  
Kathleen R. Murphy ◽  
Colin A. Stedmon
1992 ◽  
Vol 84 (6) ◽  
pp. 67-75 ◽  
Author(s):  
Gary L. Amy ◽  
Raymond A. Sierka ◽  
James Bedessem ◽  
David Price ◽  
Lo Tan

2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Svetlana Patsaeva ◽  
Daria Khundzhua ◽  
Oleg A. Trubetskoj ◽  
Olga E. Trubetskaya

Advanced fluorescence analysis within the wide range of excitation wavelengths from 230 to 510 nm accompanied with chromatography was used to study natural chromophoric dissolved organic matter (CDOM) from three freshwater Karelian lakes. The influence of excitation wavelength (λex) on fluorescence quantum yield and emission maximum position was determined. The CDOM fluorescence quantum yield has reached a minimum at λex∼270–280 nm and a maximum at λex∼340–360 nm. It was monotonously decreasing after 370 nm towards longer excitation wavelengths. Analytical reversed-phase high-performance liquid chromatography with multiwavelength fluorescence detector characterized distribution of fluorophores between hydrophilic/hydrophobic CDOM parts. This technique revealed “hidden” protein-like fluorophores for some CDOM fractions, in spite of the absence of protein-like fluorescence in the initial CDOM samples. The humic-like fluorescence was documented for all hydrophilic and hydrophobic CDOM chromatographic peaks, and its intensity was decreasing along with peaks’ hydrophobicity. On contrary, the protein-like fluorescence was found only in the hydrophobic peaks, and its intensity was increasing along with peaks’ hydrophobicity. This work provides new data on the CDOM optical properties consistent with the formation of supramolecular assemblies controlled by association of low-molecular size components. In addition, these data are very useful for understanding the CDOM function in the environment.


Water ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1617 ◽  
Author(s):  
Alexandra Tiefenbacher ◽  
Gabriele Weigelhofer ◽  
Andreas Klik ◽  
Matthias Pucher ◽  
Jakob Santner ◽  
...  

Besides the importance of dissolved organic matter (DOM) in soil biogeochemical processes, there is still a debate on how agricultural intensification affects the leaching of terrestrial DOM into adjacent aquatic ecosystems. In order to close this linkage, we conducted a short-term (45 day) lysimeter experiment with silt loam and sandy loam undisturbed/intact soil cores. Mineral (calcium ammonium nitrate) or organic (pig slurry) fertilizer was applied on the soil surface with a concentration equivalent to 130 kg N ha−1. On average, amounts of leached DOC over 45 days ranged between 20.4 mg (silt loam, mineral fertilizer) and 34.4 mg (sandy loam, organic fertilizer). Both, mineral and organic fertilization of a silt loam reduced concentration of dissolved organic carbon (DOC) in the leachate and shifted its composition towards a microbial-like signature (BIX) with a higher aromaticity (Fi) and a lower molecular size (E2:E3). However, in sandy loam only mineral fertilization affected organic matter leaching. There, lowered DOC concentrations with a smaller molecular size (E2:E3) could be detected. The overall effect of fertilization on DOC leaching and DOM composition was interrelated with soil texture and limited to first 12 days. Our results highlight the need for management measures, which prevent or reduce fast flow paths leading soil water directly into aquatic systems, such as surface flow, fast subsurface flow, or drainage water.


1984 ◽  
Vol 64 (3) ◽  
pp. 445-455 ◽  
Author(s):  
PHILIP B. DURGIN ◽  
JESSE G. CHANEY

The organic constituents of water extracts from Douglas-fir (Pseudotsuga menziesii [Mirb.] Franco var. menziesii) roots that cause kaolinite dispersion were investigated. The dissolved organic matter was fractionated according to molecular size and chemical characteristics into acids, neutrals, and bases of the hydrophilic and hydrophobic groups. The dominant fraction causing dispersion included the hydrophobic acids and organics with molecular sizes greater than 104 nominal molecular weight. Partial oxidation of the dissolved organic matter increased its carboxylic acid content and dispersion potential. Organic acids promoting kaolinite dispersion included aliphatic and aromatic carboxylic acids. The dispersing ability of a carboxylic acid was related to its charge and charge density. Kaolinite has a pH-dependent surface charge; specific adsorption of carboxyl groups makes the clay more negative and promotes dispersion. Polycarboxylic acids appear to play the major role in kaolinite dispersion by dissolved organic matter in forests. Key words: Fulvic acid, specific adsorption, carboxylic acid, fractionation


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