Organic C and N stabilization in a forest soil: evidence from sequential density fractionation
In mineral soil, organic matter (OM) accumulates mainly on and around surfaces of silt- and clay-size particles. When fractionated according to particle density, C and N concentration (per g fraction) and C/N of these soil organo-mineral particles decrease with increasing particle density across soils of widely divergent texture, mineralogy, location, and management. The variation in particle density is explained potentially by two factors: (1) a decrease in the mass ratio of organic to mineral phase of these particles, and (2) variations in density of the mineral phase. The first explanation implies that the thickness of the organic accumulations decreases with increasing particle density. The decrease in C/N can be explained at least partially by especially stable sorption of cationic peptidic compounds (amine, amide, and pyrrole) directly to mineral surfaces, a phenomenon well documented both empirically and theoretically. These peptidic compounds, along with ligand-exchanged carboxylic compounds, could then form a stable inner organic layer onto which less polar organics could sorb more readily than onto the highly charged mineral surfaces (''onion'' layering model). To explore mechanisms underlying this trend in C concentration and C/N with particle density, we sequentially density fractionated an Oregon andic soil at 1.65, 1.85, 2.00, 2.28, and 2.55 g cm{sup -3} and analyzed the six fractions for measures of organic matter and mineral phase properties. All measures of OM composition showed either: (1) a monotonic change with density, or (2) a monotonic change across the lightest fractions, then little change over the heaviest fractions. Total C, N, and lignin phenol concentration all decreased monotonically with increasing density, and {sup 14}C mean residence time (MRT) increased with particle density from ca. 150 y to >980 y in the four organo-mineral fractions. In contrast, C/N, {sup 13}C and {sup 15}N concentration all showed the second pattern. All these data are consistent with a general pattern of an increase in extent of microbial processing with increasing organo-mineral particle density, and also with an ''onion'' layering model. X-ray diffraction before and after separation of magnetic materials showed that the sequential density fractionation isolated pools of differing mineralogy, with layer-silicate clays dominating in two of the intermediate fractions and primary minerals in the heaviest two fractions. There was no indication that these differences in mineralogy controlled the differences in density of the organo-mineral particles in this soil. Thus, our data are consistent with the hypothesis that variation in particle density reflects variation in thickness of the organic accumulations and with an ''onion'' layering model for organic matter accumulation on mineral surfaces. However, the mineralogy differences among fractions made it difficult to test either the layer-thickness or ''onion'' layering models with this soil. Although sequential density fractionation isolated pools of distinct mineralogy and organic-matter composition, more work will be needed to understand mechanisms relating the two factors.
- Research Organization:
- Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)
- Sponsoring Organization:
- USDOE
- DOE Contract Number:
- W-7405-ENG-48
- OSTI ID:
- 897997
- Report Number(s):
- UCRL-JRNL-213892; TRN: US200706%%183
- Journal Information:
- Soil Biology and Biochemistry, vol. 38, N/A, October 1, 2006, pp. 3313?3324, Journal Name: Soil Biology and Biochemistry, vol. 38, N/A, October 1, 2006, pp. 3313?3324
- Country of Publication:
- United States
- Language:
- English
Similar Records
Reducing conditions, reactive metals, and their interactions can explain spatial patterns of surface soil carbon in a humid tropical forest
Subsoil organo-mineral associations under contrasting climate conditions