The sorption of organic carbon onto differing clay minerals in the presence and absence of hydrous iron oxide

Geoderma ◽  
2013 ◽  
Vol 209-210 ◽  
pp. 15-21 ◽  
Author(s):  
A.R. Saidy ◽  
R.J. Smernik ◽  
J.A. Baldock ◽  
K. Kaiser ◽  
J. Sanderman
2014 ◽  
Vol 66 (1) ◽  
pp. 83-94 ◽  
Author(s):  
A. R. Saidy ◽  
R. J. Smernik ◽  
J. A. Baldock ◽  
K. Kaiser ◽  
J. Sanderman

2016 ◽  
Vol 50 (3) ◽  
pp. 1552-1560 ◽  
Author(s):  
Daniel J. Cain ◽  
Marie-Noële Croteau ◽  
Christopher C. Fuller ◽  
Amy H. Ringwood

2004 ◽  
Vol 1 (3) ◽  
pp. 197 ◽  
Author(s):  
Julia A. Howitt ◽  
Darren S. Baldwin ◽  
Gavin N. Rees ◽  
Barry T. Hart

Environmental Context. Iron oxides, as suspended minerals or as a colloidal phase, are common in Australian freshwater systems. Freshwater systems are also loaded with carbon-based substances, ‘dissolved organic matter’, but not all is biologically available as food to freshwater organisms. However, photochemical interactions between these iron oxides and dissolved organic matter provide a mechanism for biologically resistant carbon to re-enter the food web. Suspended iron oxides thus need to be considered in carbon cycles in aquatic ecosystems. Abstract. The photochemical degradation of dissolved organic matter (DOM) derived from the leaves of River Red Gum (Eucalyptus camaldulensis) was examined, with a particular focus on the photochemical generation of CO2, consumption of O2, and the effect of particulate iron minerals on these photochemical reactions. Solutions of leaf leachate were irradiated with ultraviolet and visible light in the presence and absence of amorphous iron oxides. Addition of fresh iron oxide was found to increase the rate of photodegradation of the organic matter by up to an order of magnitude compared to the reactions without added iron oxide. The ratio of CO2 produced to O2 consumed was ~1:1 in both the presence and absence of iron oxyhydroxide. The reactivity of the iron oxides was dependent on the preparation method and decreased with increased storage time. These results suggest that photochemical reactions on particle surfaces should be considered when examining carbon transformation in aquatic ecosystems, especially at sites with potential for the production of iron oxyhydroxides.


1981 ◽  
Vol 38 (1) ◽  
pp. 68-76 ◽  
Author(s):  
Clifford N. Dahm

Removal of dissolved organic carbon (DOC) from water resulting from adsorption and microbial uptake was examined to determine the importance of biotic and abiotic pathways. Physical–chemical adsorption to components of the stream sediment or water and biotic assimilation associated with the microbial population was determined in recirculating chambers utilizing leachate from alder (Alnus rubra). Adsorptive mechanisms were further separated into interactions involving (1) specific clay minerals, (2) amorphous solid phases of hydrous aluminum and iron oxides, and (3) fine particulate organic matter. Physical–chemical adsorptive mechanisms for alder leachate removal exhibited rapid kinetic equilibration between the DOC and solid phases, but only a specific fraction of the DOC, likely containing certain chemical functional groups, was adsorbed. The amorphous aluminum and iron oxides possessed a much higher potential capacity than the clay minerals or fine particulate organics for DOC adsorption. Microbial uptake of DOC from the alder leachate was kinetically slower than adsorptive uptake. However, microbial activity was overall much more effective in the removal and degradation of the total DOC pool leached from alder leaves. Over a 48-h period, 97% of added 14C labeled leachate was removed from solution by adsorption (~ 20%) and microbial utilization (~ 77%). The rate of microbial uptake was 45 μg C/g sediment C∙h−1 or 14 mg C∙m−2∙h−1.


Clay Minerals ◽  
2002 ◽  
Vol 37 (4) ◽  
pp. 699-707 ◽  
Author(s):  
A. Mirabella ◽  
M. Egli ◽  
S. Carnicelli ◽  
G. Sartori

AbstractThe formation of clay minerals was investigated in Spodosols developed in the subalpine belt, with similar exposure, climate and age, but deriving from different parent materials. All the soils were classified as Haplic Podzols and showed the characteristic eluviation and illuviation features of Fe, Al and organic carbon. However, varying parent material lithology led to different clay mineral assemblages in the soil. Smectite could be found in the E horizons of soils developed from granodiorite and tonalite materials. Its formation was strongly dependent on the presence of chlorite in the parent material. If nearly no other 2:1 mineral components, such as chlorite, are present in the lower soil horizons, then a residual micaceous mineral becomes the dominant clay mineral. The latter derives from a mica-vermiculite interstratified mineral.


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