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1.
Estimation of the phosphorus sorption capacity of acidic soils in Ireland   总被引：4，自引：0，他引：4  
The test for the degree of phosphorus (P) saturation (DPS) of soils is used in northwest Europe to estimate the potential of P loss from soil to water. It expresses the historic sorption of P by soil as a percentage of the soil's P sorption capacity (PSC), which is taken to be α (Alox + Feox), where Alox and Feox are the amounts of aluminium and iron extracted by a single extraction of oxalate. All quantities are measured as mmol kg soil?1, and a value of 0.5 is commonly used for the scaling factor α in this equation. Historic or previously sorbed P is taken to be the quantity of P extracted by oxalate (Pox) so that DPS = Pox/PSC. The relation between PSC and Alox, Feox and Pox was determined for 37 soil samples from Northern Ireland with relatively large clay and organic matter contents. Sorption of P, measured over 252 days, was strongly correlated with the amounts of Alox and Feox extracted, but there was also a negative correlation with Pox. When PSC was calculated as the sum of the measured sorption after 252 days and Pox, the multiple regression of PSC on Alox and Feox gave the equation PSC = 36.6 + 0.61 Alox+ 0.31 Feox with a coefficient of determination (R2) of 0.92. The regression intercept of 36.6 was significantly greater than zero. The 95% confidence limits for the regression coefficients of Alox and Feox did not overlap, indicating a significantly larger regression coefficient of P sorption on Alox than on Feox. When loss on ignition was employed as an additional variable in the multiple regression of PSC on Alox and Feox, it was positively correlated with PSC. Although the regression coefficient for loss on ignition was statistically significant (P < 0.001), the impact of this variable was small as its inclusion in the multiple regression increased R2 by only 0.028. Values of P sorption measured over 252 days were on average 2.75 (range 2.0–3.8) times greater than an overnight index of P sorption. Measures of DPS were less well correlated with water‐soluble P than either the Olsen or Morgan tests for P in soil.  相似文献   

2.
Peat is commonly used as the main component of horticultural substrates, but it has a very low buffering capacity for the anionic macronutrient phosphorus (P), which can be increased by the addition of clays. The aim of this study was to characterize the P adsorption capacity of different substrate clays and to evaluate its significance for plant P uptake. Substrate clays were characterized with a single‐point batch experiment and adsorption and desorption isotherms. The data were fitted to the Langmuir equation for a calculation of the maximum adsorption capacity. Additionally, the contents of oxalate extractable Fe and Al (ΣFeox + Alox) were determined. The influence of a varying P adsorption capacity of the clays on the P availability to plants in the respective peat–clay substrates and pure peat was investigated in a growth experiment with Impatiens walleriana fertigated with 0, 17, and 35 mg P L?1 solution, respectively. The observed and calculated (Langmuir) P adsorption capacity of the clays could be well‐characterized by both the batch experiment and the adsorption isotherms and was highly correlated with the ΣFeox+Alox. A higher P adsorption capacity of the clay amendment in mixed substrates resulted in a lower P concentration in the substrate solution, while the CAT extractable P concentration (PCAT) was the same. Plant growth and shoot P concentrations were enhanced in the substrates, showing a higher P adsorption capacity, since plants were able to take up the whole amount of PCAT, and also part of the non‐CAT extractable P. However, the release rate was too low to ensure optimal plant growth, which was in accordance with the result of the desorption experiment. The absolute extent of P release was increased with the increasing P adsorption capacity of the clays and higher degree of P saturation (DPS).  相似文献   

3.
Pale-podzolic soils occupying slope positions in a small stream valley are more acidic and contain less pedogenic chlorites in the clay fraction than those soils occupying uplands. These characteristics are thought to be caused by more intensive leaching of matter from eluvial horizons due to intensive lateral interflow of soil water. Soddy-gleyic soils of the stream bottomland are rich in organic matter and have a slightly acidic reaction in the A1 horizon and an alkaline reaction in the calcareous subsoil. Both factors lead to accumulation of Feox and Alox supplied to bottomland positions from uplands and slopes and those formed in situ.  相似文献   

4.
Phosphate sorption on topsoil and subsoil samples from different soils located in the eastern part of Germany was studied. Two models were fitted to sorption data obtained after 4 and 40 d of gentle shaking. The models differ with respect to the fractions of iron and aluminium (hydr)oxides that are considered and whether the phosphate initially sorbed in the soil is taken into zccount. Oxalate-extractable P, (Pox), appears to be a major part of the total soil P. The total P sorption measured, F, was predominantly related to the amounts of amorphous iron (Feox) and aluminium (Alox). A significant relation between crystalline iron (Fed– Feox) and total P sorption was not found. Reversibly adsorbed phosphate (Pi), measured after 40 d reaction time, was a function of clay content and content of amorphous iron and aluminium (hydr)oxides.  相似文献   

5.
Abstract

The objective of the present study was to clarify the influence of volcanic ash addition on soil carbon stocks and the carbon accumulation process in brown forest soils (BFS) in Japan. The degree of volcanic ash addition to the soil was estimated according to the acid ammonium oxalate extractable aluminum (Alox) and lithic fragment contents, and their vertical distribution patterns. The BFS was classified in order of increasing volcanic ash influence on the soil into the following types: high Alox content with no gravel (H-Alox-NGv), high Alox with a high gravel content (H-Alox-Gv), moderate Alox (M-Alox), and low Alox (L-Alox), and then analyzed for carbon content, carbon amount, carbon stock, Alox amount and pyrophosphate extractable aluminum (Alpy) amount. The correlation between the carbon and Alpy amounts and the relationship between the Alpy and Alox amounts in the BFS samples indicated that the amount of carbon is determined by Al—humus complex formation, which is defined by the active Al generated from additional volcanic ash in BFS soil samples of BFS. Therefore, soils with thicker horizons and greater amounts of Alox had higher carbon levels in deeper horizons. For this reason, soil carbon stocks at depths of 0–30 cm and 0–100 cm, and in the effective soil depth of BFS, were larger and followed the order H-Alox-NGv = H-Alox-Gv > M-Alox > L-Alox. Furthermore, successive accumulations of volcanic ash on the soil surface promoted soil carbon accumulation as a result of the development of the surface horizon in H-Alox-NGv BFS. Our results suggest that volcanic ash additions control the soil carbon accumulation of forest soil in Japan.  相似文献   

6.
Twenty‐five pasture soils were sampled from high‐rainfall zones of southeastern Australia to examine relationships between soil properties, and between soil properties and P buffering capacity (PBC) measures. Correlations between PBC values and soil properties were generally poor, with the exception of oxalate‐extractable Al (Alox) (r ≥ 0.97). Predictions of PBC were further improved when clay, as well as Alox, was included in a linear regression model (r2 ≥ 0.98). When Alox and oxalate‐extractable Fe were excluded from the modelling exercise, a more complex three‐term linear regression model, including pHH2O, exchangeable H and cation exchange capacity, adequately fitted both PBC values of the 25 soils examined in this study (r2 ≥ 0.76). However, the Alox, Alox plus clay and the three‐term models gave poor predictions of the PBC values when the models were validated using 28 independent soils. These results emphasize the importance of model validation, because predictive models based on soil properties were not robust when tested across a broader range of soil types. In comparison, direct measures of PBC, such as single‐point P sorption measures, are more practical and robust methods of estimating PBC for Australian soils.  相似文献   

7.
Original and published data on the contents of X-ray amorphous oxalate-soluble compounds of Al, Fe, and Si in mesomorphic eluvial soils of cold, moderately cold, and moderately warm continental humid and semihumid regions are generalized. The groups of soils developed from mafic igneous, metamorphic, and pyroclastic rocks are considered. It is shown that the content of oxalate-soluble oxides (OSOx) in the horizons of their maximal accumulation varies from less than 1% to 20–30%; the Alox/Feox ratio varies from 1 to 6.5. The leading factor dictating the amount and quality of the OSOx in the soils is the presence or absence of volcanic glass in the parent materials. The boundary between the soils with and without volcanic glass corresponds to the OSOx content of 5% and the Al2O3ox/Fe2O3ox ratio equal to 2. These criteria are more reliable than the Alox/Feox ratio used by foreign soil scientists to specify Andosols (Alox/Feox > 2). The contents of oxalate-soluble oxides of Al and Fe do not depend on the total contents of these oxides in the parent material and seem to be related to the presence of these elements in minerals with different resistance to weathering. Under the natural conditions described in this paper, the content of OSOx shows a very weak response to zonal (temperature-controlled) climatic changes and/or to changes in the degree of humidity and the continentality of the climate.  相似文献   

8.
Abstract

The advanced classification of brown forest soils (BFS) is based on the specific properties of these soils, including the acid ammonium oxalate extractable aluminum (Alox) and lithic fragment contents, as well as their vertical distributions in the soil profile. In the present study, these properties were used to classify BFS, resulting in four types: (1) H-Alox-NGv BFS, (2) H-Alox-Gv BFS, (3) M-Alox BFS, (4) L-Alox BFS. H-Alox-NGv BFS is derived from volcanic ash characterized by a high Alox content and no lithic fragment, whereas L-Alox BFS is derived from weathered bedrock and has a low Alox content. H-Alox-Gv BFS and M-Alox BFS are derived from mixtures of volcanic ash and weathered bedrock. H-Alox-Gv BFS is characterized by high Alox content and many lithic fragments, whereas M-Alox BFS has moderate Alox content. H-Alox-NGv BFS and black soils (BLS) develop from accumulated volcanic ash, as indicated by declining Alox and clay content with decreasing depth in the surface horizons, as a result of successive additions of less-weathered volcanic ash to the soil surface.  相似文献   

9.
This study shows that mobilization of phosphate from soils under anaerobic conditions can be intimately coupled with reductive dissolution of iron from iron oxides. Among four soil samples from the reclaimed Skjernå estuary in Denmark incubated anaerobically and amended with glucose, 28–39% of the dithionite-citrate-bicarbonate-extractable iron and 10–25% of the oxalate-extractable phosphorus (Pox) were released to the soil solution after 31 days. Significant correlation (r = 0.992**) between the molar ratio Pox/(Feox + Alox) for the aerobic samples and (PP sol/Fesol) (the molar ratio between phosphate and iron in solution during anaerobic incubation), indicates that the phosphate saturation status of the soil is an important determinant of the amount of phosphate released during flooding of moderately acid soils.  相似文献   

10.
C.A. Igwe  M. Zarei  K. Stahr 《CATENA》2009,77(3):232-237
The stability of microaggregates in soils as opposed to its dispersion is a very important soil phenomenon that checks degradation arising from unguided tillage and soil erosion. Ten soils from southeastern Nigeria were sampled from their typical A and B horizons for the study. The aim was to identify the extent of colloidal stability of the soils and the forms of Fe and Al oxides in the soils contributing to their stability. The soils are mostly Ultisols and Inceptisols formed on sandstones and shale parent materials. The soils are low in soil basic cations including the soil organic carbon (SOC). The major clay mineral is kaolinite while the soil is acid in reaction. The various forms of soil Fe and Al oxides are high with the total forms of Fe and Al being most dominant and > dithionite extracted Fe and Al > oxalate extracted Fe and Al > pyrophosphate extracted Fe and Al. The water-dispersible clay and silt (WDC) and (WDSi) which are index of dispersion in most soils are low to medium thus reflecting in the low to medium dispersion ratio (DR). The clay flocculation index (CFI) and aggregated silt + clay (ASC) were moderate to high implying the high potential stability of the soils. Soil organic carbon did not seem to be contributing much to the stability of the microaggregates while oxalate and pyrophosphate extractable Fe (Feox, Fep) and to some extent total Al (Alt) were among the different forms of oxides that act as aggregating agents. We propose here that rather than SOC acting as a disaggregating agent in the soils, it might have acted in association with these oxides in a linkage or bridge such as C–P–OM–C to ensure stability of the soils.  相似文献   

11.
The sorption and desorption of phosphorus (P) from eroding soil particles in land runoff are important processes contributing to agriculturally‐driven eutrophication. We investigated the P‐exchange properties and related chemical characteristics of contrasting European agricultural soils and sediment material eroded from them under indoor (small‐scale) and outdoor (larger‐scale) rainfall simulations. Quantity‐intensity (Q/I) relationships revealed large variation in equilibrium P concentrations at zero net P sorption (EPC0) (0–10.3 mg l−1) and instantly labile P (−Q0, the amount of P to be desorbed to obtain a P equilibrium concentration of 0 mg l−1) (2–75 mg kg−1), both correlating closely with Al‐bound P and the P saturation degree of Al oxides (DPSAlox). Maximum P sorption (Qmax) (43–515 mg kg−1) also correlated most closely with Alox. The indoor and outdoor rainfall simulations produced sediments with different P sorption properties: in the indoor simulation (less kinetic energy, constant slope), the sediments had larger EPC0 values, and usually larger −Q0 values, than the sediments in the outdoor simulation (greater kinetic energy, variable slopes). Furthermore, the P exchange properties of the sediments differed from those of the bulk soil depending on the enrichment of soil P‐sorption components (Fe/Al oxides, clay). The outdoor simulation indicated that sites with gentle slopes produced sediments that were more enriched with Alox, Feox, Mnox and organic C than those with steeper slopes. In this study, when the bulk soil had an initial EPC0 greater than 1.3 mg l−1, the outdoor rainfall simulation produced sediment with smaller EPC0 and vice versa, indicating that, depending on the P status of the bulk soil, the sediment material was acting as source or sink for P during transport. However, on the basis of their EPC0 values, most eroding sediments might be expected to desorb, rather than adsorb, P when entering surface water.  相似文献   

12.
Most previous studies have limited the assessments of soil phosphorus (P) status within the plow layer. This study was to assess the impacts of crop sequences and nutrient sources on P status of a Labarre silty clay (Humic Cryaquept) profile in a frigid continental climate. Soil of the 0- to 15-, 15- to 30-, 30- to 60-, and 60- to 90-cm layers was sampled from a split-plot experiment comprising a barley (Hordeum vulgare L.) monoculture and a 3-year barley-forage rotation as main plots, and receiving mineral fertilizers (MIN) or liquid dairy manure (LDM) as subplots. A modified Hedley sequential fractionation was used to characterize soil P status. Labile P pools were more affected than stable ones by the investigated treatments. After 10 years, the MIN resulted in larger resin-P and NaHCO3-Pi, and lower NaHCO3-Po and NaOH-Po pools than the LDM in the top 30 cm of soil. The rotation resulted in larger labile Pi and Po pools than the monoculture in the 30- to 60-cm layer. The rotation associated with LDM produced the largest total labile P pool, whereas the LDM resulted in an about 20% higher degree of soil P saturation as expressed by the Pox/(Feox + Alox) molar ratio than the MIN in the 0- to 30-cm layer. Our observations stressed that the impacts of crop sequences and nutrient sources on soil labile P extended deeper into the profile than the disturbance caused by primary tillage.  相似文献   

13.
H.H. Le Riche 《Geoderma》1973,9(1):43-57
This previously described buried soil, developed in uniform parent material, was used to study the relative movements of elements and other soil components down the profile. Samples from all horizons were treated with hydrogen peroxide and ammonium oxalate, under ultra-violet light, to remove organic matter and sesquioxides, and the residues were subdivided into six particle size fractions.Downward movement of clay (< 0.5 μm) was accompanied by movement of extractable Al2O3 and Fe2O3, thus identifying these as part of the mobile fraction. The less close relationship of extractable Fe2O3 to the clay suggested that it also occurred partly in coarser aggregates. Proportions of minor elements extracted varied from < 1% for Sr to nearly complete extraction of Co, Cu and Mo in some horizons. The extractable fractions of most minor elements throughout the profile behaved more like Fe2O3 than Al2O3. In the extraction residues, nearly all elements were enriched in the clay fractions relative to the coarser fractions; this being greatest for V and Fe.  相似文献   

14.
In previous studies, Al extracted by acid ammonium acetate (Ala) or Na-pyrophosphate (Alp), rather than silt or clay content and climate conditions, was the most important factor that controls organic matter (OM) levels in volcanic soils. Here, the hypothesis was tested that Ala is a comparable method (as much as CuCl2) to quantify the proportion of Al bound to OM in allophanic soils. As far as we know, there are no previous antecedents in which selective dissolution method has been compared with this extractant. Secondly, we examine the effects of (a) Al, (b) silt plus clay content (particles size 0-53 µm) and (c) clay mineralogy on the control of organic carbon (OC) level in Chilean volcanic soils. This was achieved by sampling 16 soils series (11 Andisols, one Alfisol and four Ultisols, USDA classification) including 48 soil pedons up to 0.4 m depth. Soils were analyzed for Ala, Alp, oxalate (Alo, Sio and Feo), cold NaOH (Aln) and un-buffered salts, CuCl2 (AlCu), LaCl3 (AlLa) and KCl (Alk). We also measured the Al-humus as soluble C fraction after pyrophosphate extraction and the C associated to the silt plus clay fraction after sonication and gravity decantation. The statistical package (S)MATR was used to examine bivariate linear regressions among soil properties by computing the standardized major axis (SMA). Our results indicate that Ala had a good correspondence with Alp (R2 = 0.76) in the top soil with Ala/Alp ratio of 0.19 and both extractans presented significant and positively relationship with soil OC (R2 > 0.62). Acid ammonium acetate was as effective as AlCu to determine the Al-OM in allophanic soils. It is cheaper than AlCu and Alp and 0.5 h shaking is required compared to 2 h of AlCu and 16 h of Alp. The efficiency of the extraction was: Aln ≥ Alo > Alp > AlCu ≥ Ala > AlLa > Alk. We also found that allophane content (estimated by Al/Si ratio) was strongly correlated (R2 = 0.82) with the OC in the fine silt plus clay and that Al-humus together with C in the finest particles explained (R2 > 0.60) the largest proportion of variation of soil OC across studied soils.  相似文献   

15.
Abstract

To evaluate the relationship between the amount of available Silicon (Si) in paddy soils and their mineral properties on the Shounai Plain in Japan, which is formed from several parent materials, we evaluated the amount of available Si, the particle size distribution, the oxide composition of crystalline minerals and the amount of oxalate-extractable Si (Sio), iron (Feo) and aluminum (Alo) in the soil. The amount of available Si in the soil and the oxide content of the crystalline minerals differed among four soil groups that were distinguished by their clay mineral composition. There was no difference in the particle size distribution among the soil groups. The amount of available Si was positively related to the SiO2/Al2O3 ratio of clay, the CaO concentration of silt and fine sand, and the amounts of Sio, Feo and Alo in the soil. The amount of available Si in the soils was negative correlated with the Na2O and K2O concentrations of silt, the K2O concentration of fine sand, and the coarse sand content. These results suggest that the amount of available Si in soils is affected by the weathering resistivity of their minerals and that the particle size distribution and mineral composition are related to the available Si of the soils. Mineralogical properties, including the particle size distribution and mineral composition such as the SiO2/Al2O3 ratio × clay fraction content and the amounts of CaO and MgO in silt-sized particles, were positively correlated with the amount of available Si in the soil, but these correlations were not found for fine sand-sized particles. The Sio, Feo and SiO2/Al2O3 ratio × clay fraction contents contributed approximately 50% to the amount of available Si in the soils. The amount of available Si in the soil was divided into two groups according to the location of the paddy field. The amount of soil-available Si in the alluvial plain was affected by the geology upstream through the mineral composition.  相似文献   

16.
对太湖平原地区高产的黄泥土型水稻土的全土(<1毫米)及7个粒级(1—0.25,0.25—0.05,0.05—0.01,0.01—0.005,0.005—0.002,0.002—0.001和<0.001毫米)共8个土样,进行测定。结果表明:黄泥土粘粒部分(<0.002毫米)的粘土矿物,主要由水云母、高岭和蒙脱组成。粗粘粒级(0.002—0.001毫米)和细粘粒级(<0.001毫米)中粘土矿物的分配有明显差异;砂粒级(1—0.05毫米)中除了主要的石英外,还含有少量“铁锰砂”,所以该粒级中的SiO2含量较粉粒级(0.05—0.002毫米)的低,而Fe2O3的含量则相反,容积磁化率也较高;可塑性和膨胀性都是在<0.002毫米时才始现。上述特点与作者过去所研究的白土型水稻土类似。但是,与国内外报道的几种旱地土壤的资料有所不同。  相似文献   

17.
Phosphate sorption was studied in samples (0 - 20 cm depth) of five soils from Egypt (pH 7.4 - 8.7), four soils from Ethiopia (pH 3.9 - 5.3) and six soils from Germany (pH 3.3 - 7.2). Sorption parameters were calculated according to Pagel and Van Huay (1976) and according to Langmuir (Syers et al., 1973). Phosphate sorption parameters and oxalate extractable Fe and Al (Feox, Alox) were related to the phosphate uptake by young rye plants in Neubauer pot experiments. P sorption parameter after Pagel and Van Huay (A) correlated significantly positively with the Feox and Alox content in acid (r = 0.73) as well as in calcareous soils (r = 0.89) if the whole equilibrium concentration range (0 - 14 mg P/L) was considered. The relations calculated after Langmuir (B) were similar. P uptake by rye in acid soils was negatively correlated with the affinity constant n (r = ?0.76, (A)). In calcareous soils, a negative correlation between P uptake and affinity constant was calculated in the lower P equilibrium range (0 - 2.8 mg P/L) only for (B). Thus, P uptake decreased with increasing strength of P bonding to soil. From these results it is concluded that phosphate sorbed to Fe/Al oxides is an important P source for plants in acid and calcareous soils.  相似文献   

18.
There has been less concern about soil mineralogical alteration than about soil physical, chemical and biological changes induced by termite nest-building activity. Furthermore, much less attention has been paid to free sesquioxides than to phyllosilicate minerals. In the present study, we conducted field morphological observations and selective dissolution analysis to characterize free sesquioxides in termite (Macrotermes bellicosus) mounds as compared with surrounding pedons in different toposequence positions, i.e., seasonally flooded valley bottom, hydromorphic fringe and well-drained upland sites. Distinctive redoximorphic features, such as surface yellowish layers on mound structures from the fringe site, indicate possible alteration of iron sesquioxide forms in the mounds due to the transportation of soil from reductive (aquic subsoil) to oxidative (epigeal mound) environments by the nest-building activity of M. bellicosus. On the other hand, the iron-soluble content in the dithionite-citrate-bicarbonate (DCB) system (Fed) was generally higher in the mound structures than at the adjacent sub-surface (Ap2) horizon at each toposequence position, while there was less difference in the content of acid ammonium oxalate (AAO) extractable iron (Feo) as compared to Fed. As a consequence, the iron activity index (Fed/Feo ratio) was found for the most part to be lower in the mound structures than in the neighboring Ap2 horizon. In addition, the content of Fed, AAO-soluble Al (Alo) and DCB-extractable Al (Ald) was significantly correlated with clay content in these soils. These findings suggest that M. bellicosus preferentially collects clay particles, probably from the clay-rich subsoils, such as the argillic horizon, which has been formed by the co-migration of phyllosilicate minerals and relatively crystalline sesquioxides. The species then likely incorporates them into the mounds, which induces an increase in the Fed content relative to that of Feo, resulting in a decreased iron activity index in the mound structures.  相似文献   

19.
Submerged macrophytes are commonly used for the environmental engineering of the controlling of shallow lake eutrophication, and are also an effective and valid alternative for the remediation of eutrophic water bodies, not only under experimental conditions but also under natural conditions. Therefore, the effects of submerged macrophytes on the improvement of shallow lake water quality have been intensively investigated. But the mechanism was not well understood, especially the mechanism of the effects of submerged macrophytes on the exchange of nutrients at sediment–water interface in shallow lakes. This study selected a familiar submerged macrophyte Hydrilla verticillata in China and evaluated the effects of H. verticillata on the phosphate retention and release at the lake sediment–water interface in a simulated condition. The effects of H. verticillata on the phosphate sorption isotherm, phosphorus (P) availability were investigated and the subsequent kinetics of P release was also measured by repeated extraction with CaCl2 solution. Exchangeable Ca and ammonium oxalate-extractable Fe (Feox) and Al (Alox) of the sediments were also determined. The results show that the contents of organic matter, cationic exchange capacity (CEC), Ca, Fe, Al, exchangeable Ca, Feox and Alox of the sediments with H. verticillata were higher than those of the control sediments, and the contents of total phosphorus (TP), Olsen-P and reactive dissolve phosphorus (RDP) were lower. The sediments with H. verticillata had stronger P sorption ability and weaker ability of P release. H. verticillata did not significantly affect the trends of the sorption isotherms and kinetics of the released P on the sediments. H. verticillata can significantly increase the ability of P sorption, decrease in the ability of P desorption on sediments was one of the mechanism that maintained lower P levels of the overlying water through affecting the contents of organic matter, CEC, Ca, Fe, Al, exchangeable Ca, Feox and Alox in sediments.  相似文献   

20.
Recent studies with Andisols show that the carbon (C) stabilization capacity evolves with soil age relative to the evolution of the mineral phase. However, it is not clear how soil mineralogical changes during pedogenesis are related to the composition of soil organic matter (SOM) and 14C activity as an indicator for the mean residence time of soil organic matter (SOM). In the present study, we analyzed the contribution of allophane and metal–SOM complexes to soil C stabilization. Soil organic matter was analyzed with solid-state 13C nuclear magnetic resonance spectroscopy. Additionally, the soil was extracted with Na-pyrophosphate (Alp, Fep) and oxalate (Alo, Sio, and Feo). Results supported the hypothesis that allophane plays a key role for SOM stabilization in deep and oldest soil, while SOM stabilization by metal (Al and Fe) complexation is more important in the surface horizons and in younger soils. The metal/Cp ratio (Cp extracted in Na-pyrophosphate), soil pH, and radiocarbon age seemed to be important indicators for formation of SOM–metal complexes or allophane in top- and subsoils of Andisols. Changes in main mineral stabilization agents with soil age do not influence SOM composition. We suggest that the combination of several chemical parameters (Alp, Fep and Cp, metal/Cp ratio, and pH) which change through soil age controls SOM stabilization.  相似文献   

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