Waterlogging and soil reduction affect the amount and apparent molecular weight distribution of dissolved organic matter in wetland soil: a laboratory study

被引:12
作者
Rouwane, Asmaa [1 ]
Grybos, Malgorzata [1 ]
Bourven, Isabelle [1 ]
Rabiet, Marion [1 ]
Guibaud, Gilles [1 ]
机构
[1] Univ Limoges, GRESE, 123 Ave Albert Thomas, F-87060 Limoges, France
关键词
dissolved organic carbon; humic substances; hydromorphic soil; proteins; reducing conditions; SIZE-EXCLUSION CHROMATOGRAPHY; AQUATIC HUMIC SUBSTANCES; CHEMICAL-COMPOSITION; MINERAL SURFACES; CARBON; FRACTIONS; ADSORPTION; NITROGEN; WATER; SPECTROSCOPY;
D O I
10.1071/SR16308
中图分类号
S15 [土壤学];
学科分类号
0903 ; 090301 ;
摘要
The release of dissolved organic matter (DOM) from wetland soils is an important pathway for the input of organic compounds into adjacent aquatic environments. In the present study we investigated, under controlled laboratory conditions, the quantity and quality of DOM released from a wetland soil subject to waterlogging and reducing conditions. Three soil redox conditions (oxic, moderately reducing and advanced reducing) were distinguished based on nitrate, ferrous ions and sulfate concentrations in soil solution. Under each redox condition, the quantity (dissolved organic carbon (DOC), humic substances and peptides plus proteins (P-PN) and quality (aromaticity; specific ultraviolet absorbance at 254 nm (SUVA254nm)) and apparent molecular weight (aMW) distribution) of DOM were investigated. The results showed that soil redox condition affects the amount and properties of mobilised DOM. The rate of DOM release and SUVA254 values were highest during the transition from oxic to moderately reducing conditions, whereas both stabilised during progression to advanced reducing conditions. In addition, the mobilised DOM is expected to be more reactive because of an increase in polar substituents in aromatic structures between oxic and moderately reducing conditions. During the development of moderately reducing conditions, dissolved humic substances increased significantly, whereas their aMW distribution (between 500 and 6000) remained constant for each of the three different redox conditions. In contrast, the quantity of dissolved P-PN remained low and steady under the three redox conditions, whereas the aMW distribution of protein-like and microbial by-product-like compounds decreased during the development of reducing conditions (aMW of compounds between 100 and > 100 000).
引用
收藏
页码:28 / 38
页数:11
相关论文
共 72 条
  • [1] Aiken G. R., HUMIC SUBSTANCES SOI
  • [2] The pitfalls of protein quantification in wastewater treatment studies
    Avella, A. C.
    Goerner, T.
    de Donato, Ph.
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 2010, 408 (20) : 4906 - 4909
  • [3] Bock P, 2014, CHERNOZEMS AUSTRIAN
  • [4] REDOX POTENTIALS
    BOHN, HL
    [J]. SOIL SCIENCE, 1971, 112 (01) : 39 - &
  • [5] Determination of changes in wastewater quality through a treatment works using fluorescence spectroscopy
    Bridgeman, John
    Baker, Andy
    Carliell-Marquet, Cynthia
    Carstea, Elfrida
    [J]. ENVIRONMENTAL TECHNOLOGY, 2013, 34 (23) : 3069 - 3077
  • [6] Arsenite and arsenate binding to dissolved humic acids: Influence of pH, type of humic acid, and aluminum
    Buschmann, Johanna
    Kappeler, Alexandra
    Lindauer, Ursula
    Kistler, David
    Berg, Michael
    Sigg, Laura
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2006, 40 (19) : 6015 - 6020
  • [7] Calvet R., 2011, MATIERES ORGANIQUES
  • [8] Fluorescence excitation - Emission matrix regional integration to quantify spectra for dissolved organic matter
    Chen, W
    Westerhoff, P
    Leenheer, JA
    Booksh, K
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (24) : 5701 - 5710
  • [9] MOLECULAR-WEIGHT, POLYDISPERSITY, AND SPECTROSCOPIC PROPERTIES OF AQUATIC HUMIC SUBSTANCES
    CHIN, YP
    AIKEN, G
    OLOUGHLIN, E
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1994, 28 (11) : 1853 - 1858
  • [10] Reaction of forest floor organic matter at goethite, birnessite and smectite surfaces
    Chorover, J
    Amistadi, MK
    [J]. GEOCHIMICA ET COSMOCHIMICA ACTA, 2001, 65 (01) : 95 - 109