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1.
The dependency of the retention of dissolved organic carbon (DOC) on mineral phase properties in soils remains uncertain especially at neutral pH. To specifically elucidate the role of mineral surfaces and pedogenic oxides for DOC retention at pH 7, we sorbed DOC to bulk soil (illitic surface soils of a toposequence) and corresponding clay fraction (< 2 μm) samples after the removal of organic matter and after removal of organic matter and pedogenic oxides. The DOC retention was related to the content of dithionite‐extractable iron, specific surface area (SSA, BET‐N2 method) and cation exchange capacity (pH 7). The reversibility of DOC sorption was determined by a desorption experiment. All samples sorbed 20–40 % of the DOC added. The DOC sorption of the clay fractions explained the total sorption of the bulk soils. None of the mineral phase properties investigated was able to solely explain the DOC retention. A sorption of 9 to 24 μg DOC m–2 indicated that DOC interacted only with a fraction of the mineral surface, since loadings above 500 μg m–2 would be expected for a carbon monolayer. Under the experimental conditions used, the surface of the silicate clay minerals seemed to be more important for the DOC sorption than the surface of the iron oxides. The desorption experiment removed 11 to 31 % of the DOC sorbed. Most of the DOC was strongly sorbed.  相似文献   

2.
Soil minerals are known to influence the biological stability of soil organic matter (SOM). Our study aimed to relate properties of the mineral matrix to its ability to protect organic C against decomposition in acid soils. We used the amount of hydroxyl ions released after exposure to NaF solution to establish a reactivity gradient spanning 12 subsoil horizons collected from 10 different locations. The subsoil horizons represent six soil orders and diverse geological parent materials. Phyllosilicates were characterized by X-ray diffraction and pedogenic oxides by selective dissolution procedures. The organic carbon (C) remaining after chemical removal of an oxidizable fraction of SOM with NaOCl solution was taken to represent a stable organic carbon pool. Stable organic carbon was confirmed as older than bulk organic carbon by a smaller radiocarbon (14C) content after oxidation in all 12 soils. The amount of stable organic C did not depend on clay content or the content of dithionite–citrate-extractable Fe. The combination of oxalate-extractable Fe and Al explained the greatest amount of variation in stable organic C (R2 = 0.78). Our results suggest that in acid soils, organic matter is preferentially protected by interaction with poorly crystalline minerals represented by the oxalate-soluble Fe and Al fraction. This evidence suggests that ligand exchange between mineral surface hydroxyl groups and negatively charged organic functional groups is a quantitatively important mechanism in the stabilization of SOM in acid soils. The results imply a finite stabilization capacity of soil minerals for organic matter, limited by the area density of reactive surface sites.  相似文献   

3.
The influence of the soil mineral phase on organic matter storage was studied in loess derived surface soils of Central Germany. The seven soils were developed to different genetic stages. The carbon content of the bulk soils ranged from 8.7 to 19.7 g kg—1. Clay mineralogy was confirmed to be constant, with illite contents > 80 %. Both, specific surface area (SSA, BET‐N2‐method) and cation exchange capacity (CEC) of bulk soils after carbon removal were better predictors of carbon content than clay content or dithionite‐extractable iron. SSA explained 55 % and CEC 54 % of the variation in carbon content. The carbon loadings of the soils were between 0.57 and 1.06 mg C m—2, and therefore in the ”︁monolayer equivalent” (ME) level. The increase in SSA after carbon removal (ΔSSA) was significantly and positively related to carbon content (r2 = 0.77). Together with CEC of carbon‐free samples, ΔSSA explained 90 % of the variation in carbon content. Clay (< 2 μm) and fine silt fractions (2—6.3 μm) contained 68—82 % of the bulk soil organic carbon. A significantly positive relationship between carbon content in the clay fraction and in the bulk soil was observed (r2 = 0.95). The carbon pools of the clay and fine silt fractions were characterized by differences in C/N ratio, δ13C ratio, and enrichment factors for carbon and nitrogen. Organic matter in clay fractions seems to be more altered by microbes than organic matter in fine silt fractions. The results imply that organic matter accumulates in the fractions of smallest size and highest surface area, apparently intimately associated with the mineral phase. The amount of cations adhering to the mineral surface and the size of a certain and specific part of the surface area (ΔSSA) are the mineral phase properties which affect the content of the organic carbon in loess derived arable surface soils in Central Germany most. There is no monolayer of organic matter on the soil surfaces even if carbon loadings are in the ME level.  相似文献   

4.
We used the specific surface area (SSA), the cation exchange capacity (CEC) and the content of dithionite‐extractable iron (Fed) to predict the content of organic carbon in illitic clay fractions of topsoils from loess. We determined SSA (BET‐N2 method) and CEC of clay fractions after removing organic C or reducing oxides or both. The CEC and the SSA of the carbon‐ and oxide‐free clay fraction explained 56% and 54% of the variation in C content, respectively. The Fed content of the clay fractions was strongly and negatively related to the C content, and with the SSA of the carbon‐free clay fraction it predicted C content almost completely (R2 = 0.96). The results indicate that the amount of cations adhering to the silicate clay minerals and the size of the silicate mineral surface area are important properties of the mineral phase for the storage potential of C. The reason for the negative relation between iron oxides and C content remains unclear.  相似文献   

5.
The organic matter in soils may be stabilized by its interactions with minerals. We have studied such interactions in a Haplic Alisol under forest in which clay and organic matter have migrated from an eluvial A horizon to accumulate in an illuvial B horizon. We have tried to trace the fate of organic matter in these horizons (Ah and Bvt) by determining clay mineralogy, carbon and nitrogen content, hydrolysable amino acids, lignin signature by alkaline CuO oxidation and carbon species by 13C CPMAS NMR of bulk soils and particle‐size fractions. In both horizons, most of the organic matter was present in O–alkyl and methylene structures, each contributing one‐third to the bulk organic matter. In the Ah horizon the ratios of carbon‐to‐nitrogen, and yields for lignin and hydrolysable amino acids decreased as the particle‐size class decreased, but side‐chain oxidation of lignin compounds increased with decreasing particle size. In contrast to previous observations, the proportions of O–alkyl carbon increased as particle size decreased, constituting a major proportion of the organic carbon in the clay‐size fractions from both the Ah and Bvt horizons (≥ 38%), while proportions of methylene carbon decreased. Illite was the dominant mineral in the fraction ≤ 6 μm, whereas the mobile fine clay fraction (<0.2 μm) was rich in smectites – minerals with large surface areas. Our results support the hypothesis that potentially labile organic matter, such as O–alkyl carbon typically present in polysaccharides, may be stabilized against further degradation in organomineral complexes.  相似文献   

6.
Abstract

Chemical properties of hydrophobic acid (HoA) fractions in water-soluble organic matter in soil and water are concerned with its interactions with mineral soil surfaces and organic pollutants. In 2004 we examined the seasonal and vertical changes in chemical properties of the HoA fraction in a Cambisol profile and compared these properties with those in the HoA fraction of an adjacent stream (aquatic humic substances) in a temperate forested watershed using high performance size exclusion chromatography (HPSEC) and 1H and 13C nuclear magnetic resonance (NMR) spectroscopy. The HoA fractions from Oi, Oe/Oa, A and B horizon soils in summer had lower O-alkyl C proportions than those recorded in samples in other seasons. The proportions of aromatic C in HoA fractions from A and B horizons were highest in summer. These seasonal variations were less significant than variations with soil depth. O-alkyl C proportions in HoA fractions decreased with increasing soil depth from the Oi to the A horizon. The HoA fractions from the B horizon showed a higher alkyl C proportion than samples from other horizons in winter and spring. These changes with soil depth from the Oi to A horizons might result from selective utilization of carbohydrate carbon by microorganisms, whereas those in the B horizon may result from sorption to mineral surfaces. The HoA fractions in the stream were similar in relative molecular weight, distribution of each type of proton and carbon species in HoA fractions from the B horizon, whereas stream HoA fractions collected in summer would be derived from organic horizons. This indicated that vertical changes in the chemical properties of HoA fractions in soil and pathways of water to the stream would largely affect the chemical properties of HoA fractions in the stream.  相似文献   

7.
Summary The concentrations of organic C and total N in five different particle-size fractions were studied under different mineral and organic fertilizer regimens by examining soil samples from the 34-year-old soil-formation pot experiment Hu 3 in Rostock. The C and N concentrations were generally highest in the clay fraction and decreased in the order medium silt >fine silt >coarse silt and sand. For nearly all years and size fractions the following order was obtained for C and N concentrations under the various fertilizer regimens: Compost >farmyard manure >straw + mineral fertilizer >mineral fertilizer. The various particle-size fractions and fertilizer regimens differed in the development of soil organic matter levels. Consequently, characteristic redistributions were found in the proportions of C and N in the various particle-size fractions, particularly after organic fertilizer was no longer applied (years 20–34). This experimental phase was characterized by decreased organic C and increased total N concentrations, and increased proportions of C and N in the clay-size at the expense of the sand fractions.  相似文献   

8.
According to recent conceptual models, the organic carbon (OC) of soils can be divided into OC fractions of increasing stability from labile free OC to resistant OC associated with the soil mineral phase. In this study, we present a method for quantifying two OC fractions based on soil aggregate–size fractionation and the N2 gas–adsorption method. For this purpose, we analyzed soil material of the plow layer of a Haplic Chernozem subjected to different fertilizer treatments (no fertilizer, mineral fertilizer, mineral and organic fertilizer). The total organic‐C concentration (TOC) and the clay content of the different size fractions were determined as well as the specific surface area (SSAmineral) and the sample pore volume after thermal oxidation (OC‐free). The TOC of the different soil‐aggregate fractions was linearly related to SSAmineral. Clay‐associated OC and nonassociated OC fractions of the different soil samples were quantified using two methods based on the OC surface loading at the clay fraction. The application of organic fertilizer increased the amount of nonassociated OC but hardly affected the concentration of clay‐associated OC. This finding agrees with previous studies on C dynamics in soils and indicates a finite capacity of soil materials to sequester OC. Even without any addition of organic fertilizer, the mineral phase of the analyzed soil material appears to be C‐saturated.  相似文献   

9.
The composition of functional light soil organic matter pools of arable Cambisols with a gradient in clay content was investigated. Soil texture differences originate from increasing loess admixture to the parent material (coarse‐grained tertiary sediments). Using density fractionation in combination with ultrasonic dispersion, two types of particulate organic matter (POM) were obtained: (1) free POM and (2) POM occluded in soil aggregates. Both POM fractions were analyzed by elemental analysis (C, N) and CPMAS 13C NMR spectroscopy. With increasing clay content the amount of organic carbon stored in the occluded POM fraction increased considerably, whereas the amounts of free POM were not related to the soil clay content. With increasing soil clay contents increasing proportions of O‐alkyl C and decreasing proportions of aryl C were found for both POM fractions. The occluded POM fraction showed a higher degree of degradation as indicated by lower amounts in O‐alkyl carbon. A lower degree of POM degradation was associated with higher clay contents. Higher soil clay contents promoted the conservation of POM with a low degree of alteration. This effect of soil texture was found to be highly significant when the aryl C : O‐alkyl C ratio was used as indicator for POM decomposition rather than the alkyl C : O‐alkyl C ratio.  相似文献   

10.
The study examined the influence of compost and mineral fertilizer application on the content and stability of soil organic carbon (SOC). Soil samples collected from a long-term field experiment were separated into macroaggregate, microaggregate, and silt + clay fractions by wet-sieving. The experiment involved seven treatments: compost, half-compost N plus half-fertilizer N, fertilizer NPK, fertilizer NP, fertilizer NK, fertilizer PK, and control. The 18-year application of compost increased SOC by 70.7–121.7%, and mineral fertilizer increased by 5.4–25.5%, with no significant difference between control soil and initial soil. The C mineralization rate (rate per unit dry mass) in microaggregates was 1.52–2.87 mg C kg−1 day−1, significantly lower than in macroaggregate and silt + clay fractions (P < 0.05). Specific C mineralization rate (rate per unit SOC) in silt + clay fraction amounted to 0.48–0.87 mg C g−1 SOC day−1 and was higher than in macroaggregates and microaggregates. Our data indicate that SOC in microaggregates is more stable than in macroaggregate and silt + clay fractions. Compost and mineral fertilizer application increased C mineralization rate in all aggregates compared with control. However, compost application significantly decreased specific C mineralization rate in microaggregate and silt + clay fractions by 2.6–28.2% and 21.9–25.0%, respectively (P < 0.05). By contrast, fertilizer NPK application did not affect specific C mineralization rate in microaggregates but significantly increased that in silt + clay fractions. Carbon sequestration in compost-amended soil was therefore due to improving SOC stability in microaggregate and silt + clay fractions. In contrast, fertilizer NPK application enhanced SOC with low stability in macroaggregate and silt + clay fractions.  相似文献   

11.
The retention of dissolved organic matter in soils is mainly attributed to interactions with the clay fraction. Yet, it is unclear to which extent certain clay‐sized soil constituents contribute to the sorption of dissolved organic matter. In order to identify the mineral constituents controlling the sorption of dissolved organic matter, we carried out experiments on bulk samples and differently pretreated clay‐size separates (untreated, organic matter oxidation with H2O2, and organic matter oxidation with H2O2 + extraction of Al and Fe oxides) from subsoil horizons of four Inceptisols and one Alfisol. The untreated clay separates of the subsoils sorbed 85 to 95% of the dissolved organic matter the whole soil sorbed. The sorption of the clay fraction increased when indigenous organic matter was oxidized by H2O2. Subsequent extraction of Al and Fe oxides/hydroxides caused a sharp decrease of the sorption of dissolved organic matter. This indicated that these oxides/hydroxides in the clay fraction were the main sorbents of dissolved organic matter of the investigated soils. Moreover, the coverage of these sorbents with organic matter reduced the amount of binding sites available for further sorption. The non‐expandable layer silicates, which dominated the investigated clay fractions, exhibited a weak sorption of dissolved organic matter. Whole soils and untreated clay fractions favored the sorption of ”︁hydrophobic” dissolved organic matter. The removal of oxides/hydroxides reduced the sorption of the lignin‐derived ”︁hydrophobic” dissolved organic matter onto the remaining layer silicates stronger than that of ”︁hydrophilic” dissolved organic matter.  相似文献   

12.
黄土高原旱地连续施用锰肥的土壤效应研究   总被引：1，自引：0，他引：1  
采用连续浸提形态分级方法，研究了连续施用锰肥17a后锰的土壤化学特性变化。结果表明：经过长期连续施用锰肥，土壤全锰和DTPA—Mn含量增加不多。土壤DTPA—Mn含量随试验时间的延长呈增加趋势，施锰土壤有效锰提高不多，土壤DTPA—Mn含量只增加了0．4～1．7mgkg^-1。土壤中的锰主要以矿物态存在，占土壤全锰含量的比例为87．3％～91.8％。碳酸盐态、氧化锰态和紧结有机态锰占全锰的比例相当，土壤中各形态锰按含量大致呈矿物态〉碳酸盐态〉氧化锰态〉紧结有机态〉松结有机态〉交换态的顺序。施入土壤的锰肥有91．1％～98．6％进入碳酸盐结合态、氧化锰结合态、紧结有机态和矿物态，只有很少一部分仍留在有效态锰库中。交换态和松结有机态锰对土壤锰的有效性起着主要作用，可以反映土壤锰的供给状况，碳酸盐态和紧结有机态锰不能反映土壤锰的有效性。  相似文献   

13.
We studied the quantitative and qualitative changes of soil organic matter (SOM) due to different land uses (arable versus grassland) and treatments (organic manure and mineral fertilizer) within an agricultural crop rotation in a long‐term field experiment, conducted since 1956 at Ultuna, Sweden, on a Eutric Cambisol. The organic carbon (OC) content of the grassland plot was 1.8 times greater than that of the similarly fertilized Ca(NO3)2 treated cropped plots. The comparison of two dispersion techniques (a low‐energy sonication and a chemical dispersion which yield inherent soil aggregates) showed that increasing OC contents of the silt‐sized fractions were not matched by a linear increase of silt‐sized aggregates. This indicated saturation of the aggregates with OC and a limited capacity of particles to protect OC physically. Thermogravimetric analyses suggested an increase of free organic matter with increasing OC contents. Transmission FT‐IR spectroscopy showed relative enrichment of carboxylic, aromatic, CH and NH groups in plots with increasing OC contents. The silt‐sized fractions contained the largest SOM pool and, as revealed by 13C NMR spectroscopy, were qualitatively more influenced by the plant residue versus manure input than the clay fractions. Alkyl and O‐alkyl C in the silt‐sized fractions amounted to 57.4% of organic carbon in the animal manure treated plots and 50–53% in the other treatments.  相似文献   

14.
We studied the impact of climate, soil texture and iron mineralogy on the content and composition of organic matter in Ferralsols along a climosequence in southern Brazil. We characterized the organic matter by solid‐state cross‐polarization magic angle spinning (CPMAS) 13C nuclear magnetic resonance (NMR) spectroscopy. The organic matter content in the Ferralsols increased from the lowest to the highest sites (440–950 m altitude) as a result of the increase in humidity and the decrease in temperature. This influence was more pronounced in the heavy clayey Ferralsols, suggesting that the accumulation of organic matter was enhanced by organo‐mineral interactions. Iron oxides contributed to the stabilization of the organic matter in these soils, which was dominated by O–alkyl C structures followed by aromatic and alkyl C groups. The aromatic C contribution to the total organic C increases with depth at the expense of O–alkyl C, regardless of the site altitude and climate. Although the impact of the environment on the amount of organic matter and its chemical composition is confirmed, our results clearly show that this is so only for the surface horizons. With increasing soil depth the climatic influence decreased, showing that other factors become more important for the accumulation of organic matter.  相似文献   

15.
Summary Soil was sampled in autumn 1984 in the 132 field (sandy loam soil) of the Askov long-term experiments (started in 1894) and fractionated according to particle size using ultrasonic dispersion and sedimentation in water. The unmanured plot and plots given equivalent amounts of N (1923–1984 annual average, 121 kg N/ha) in either animal manure or mineral fertilizer were sampled to a depth of 15 cm, fractionated and analysed for C and N. Mineral fertilizer and animal manure increased the C and N content of whole soil, clay (<2 m) and silt (2–20 m) size fractions relative to unmanured samples, while the C content of the sand size fractions (fine sand 1, 20–63 m; fine sand 2, 63–200 m; coarse sand, 200–2000 m) was less affected. Clay contained 58% and 65°70 of the soil C and N, respectively. Corresponding values for silt were 30% and 26%, while sand accounted for 10% of the soil C. Fertilization did not influence this distribution pattern. The C : N ratio of the silt organic matter (14.3) was higher and that of clay (10.6) lower than whole-soil C:N ratios (12.0). Fertilization did not influence clay and silt C : N ratios. Animal manure caused similar relative increases in the organic matter content of clay and silt size fractions (36%). In contrast, mineral fertilizer only increased the organic matter content of silt by 21% and that of clay by 14%.  相似文献   

16.
The 4‐year application of pig‐manure compost (PMC) to crop fields in Jiangsu significantly increased organic‐C and total N concentrations compared to chemical fertilization and control treatment. To identify the soil processes that led to these changes, 13C cross‐polarization magic‐angle spinning nuclear‐magnetic resonance (13C CPMAS NMR) and dipolar‐dephasing nuclear‐magnetic‐resonance spectroscopy (DD NMR) were conducted on soil organic matter (SOM) fractions separated by wet‐sieving and density fractionation procedures. This allowed characterization of the SOM quality under three contrasting fertilizer regimes. The results indicate that PMC application can alter the distribution of functional groups and improve alkyl C‐to‐O‐alkyl C ratios compared to chemical‐fertilizer treatment (CF). Alkyl C contents were increased from macroaggregate fractions (> 2 mm) to microaggregate fractions (0.05–0.25 mm) for all treatments, suggesting that recalcitrant material accumulates in the microaggregate fractions. The O‐alkyl C contents were decreased from macroaggregate fractions (> 2 mm) to microaggregate fractions (0.05–0.25 mm) under CF and PMC treatments, while no consistent trend was found for the control (NF) treatment. The alkyl C‐to‐O‐alkyl C ratios in macroaggregates were lower than those in microaggregates, indicating that the degrees of SOM decomposition were lower in macroaggregates compared to microaggregates. In all aggregate‐size classes, the amount of organic matter appeared to depend on the fertilization regime. This study provides useful information regarding the buildup of organic material in soil from long‐term manure‐compost enrichment.  相似文献   

17.
The iron oxides fractions of four major physiographic units obtained from a transect of calcareous materials were studied to assess the effects of key pedogenic processes and local hydrology conditions as well as physiographic units in controlling iron oxides forms in the north-west of Iran. Samples from different horizons belonging to six pedons were selected and analyzed for soil physicochemical properties, clay minerals, and Fe oxides forms (Fed, Feo, Fep). In general, the soils indicated some variation in the concentration of iron oxides that could be related to rate of weathering, pedogenic accumulations, geomorphologic conditions (as results of different in physiographic units), wet and dry cycle, and organic matter. A wide relative variation in mean values of Fed (6.4–9.9 g kg?1), Feo (2.9–4 g kg?1), and Fep (0.68–1.3 g kg?1) was observed among physiographic units. On the plateau unit, the presence of the most stable geomorphologic conditions and high rate in situ weathering (reflected in clay content), coupled with minor deposition of sediment suggest that the soils have more dynamic conditions than other units, reflecting in the greatest amount Fed and the lowest Feo/Fed ratio. Fed content of the soils containing less clay content (15–25%) was significantly different from those with greater clay content (25–35%).  相似文献   

18.
Clay minerals have a major role in soil aggregation because of their large specific surface area and surface charges, which stimulate interactions with other mineral particles and organic matter. Soils usually contain a mixture of clay minerals with contrasting surface properties. Although these differences should result in different abilities of clay minerals regarding aggregate formation and stabilization, the role of different clay minerals in aggregation has been seldom evaluated. In this study, we took advantage of the intrinsic mineral heterogeneity of a temperate Luvisol to compare the role of clay minerals in aggregation. First, grassland and tilled soil samples were separated in water into aggregate‐size classes based on the aggregate hierarchy model. Then, clay mineralogy and organic C in the aggregate‐size classes were analysed. Interstratified minerals containing swelling phases accumulated in aggregated fractions compared with free clay fractions under the two land‐uses. The accumulation increased with decreasing aggregate size from large macroaggregates (> 500 µm) to microaggregates (50–250 µm). Carbon content and carbon‐to‐nitrogen ratio followed the opposite trend. This fully supports the aggregate hierarchy model, which postulates an increasing importance of mineral reactivity in smaller aggregates than in larger aggregates in which the cohesion relies mostly on physical enmeshment by fungal hyphae or small roots. Consequently, differences in the proportion of the different 2:1 clay minerals in soils can influence their structure development. Further research on the links between clay mineralogy and aggregation can improve our understanding of mechanisms of soil resistance to erosion and organic matter stabilization.  相似文献   

19.
l3C–nuclear magnetic resonance (NMR) spectra taken using magic–angle spinning (MAS), cross polarization (CP) and with total suppression of side bands (TOSS) are reported for soils from two long–term field experiments. One set of soils was from the Broadbalk Experiment at Rothamsted, UK (monoculture of winter wheat since 1843) and the other was from the Lermarken site of the Askov Long–Term Experiment on Animal Manure and Mineral Fertilizers (arable rotation since 1894). At both sites soil samples were taken from three fertilizer treatments: nil, inorganic fertilizers, animal manure. Spectra were obtained from whole soil samples and from the size fractions clay (<2 μrn), silt (2–20 μm) and, in some cases, sand (20–2000 μm). Comparison of the total strengths of the 13C–NMR signal for each size separate in relation to its total organic C content shows that clay, particularly, contains large percentages of C not detected by NMR because of the large magnetic susceptibilities of the soil minerals. It is proposed that the observed signals come from the more labile pools of soil organic matter (SOM), on the presumption that these pools are less closely associated with soil minerals and iron oxides and are likely to be less protected from microbial or enzymic decomposition. For both Rothamsted and Askov, functional groups in the 45–110 ppm region (N– and O–alkyls) dominate in the spectra for whole soils, with aromatics (110–160 ppm) and alkyls (0–45 ppm) signals being the next prominent. In the Askov whole soil samples 13C–NMR revealed no differences between nil, inorganic fertilizer and animal manure treatments but in the Rothamsted whole soil there were some small differences. Clay and silt fractions from Askov contain more alkyls and less aromatics than those from Rothamsted. For both sites clay in enriched in alkyls and depleted in aromatics relative to silt. Clay from Askov, but not Rothamsted, contains more N–alkyls (45–65 ppm) and less acetals (90–110 ppm) than silt. O–alkyls (65–90 ppm) account for more than 20% of the total signal in clay and silt from both sites. Fertilization regimes have not significantly affected the chemical composition of SOM associated with clay– and silt–sized fractions in the soils at either site. We conclude that the chemical composition of SOM is determined primarily by the interaction between the organisms responsible for decomposition and the mineral soil matrix rather than the nature of substrate input.  相似文献   

20.
Recent concerns about climate change and atmospheric greenhousegas concentrations have demonstrated the importance ofunderstanding ecosystem C source/sink relationships. Soilorganic matter fractionation was carried out in three paired,forested watershed sites where one of each watershed pairrepresented a different ecosystem perturbation. Theperturbations were 8 years of experimental N amendments at theBear Brook Watershed in Maine (BBWM), a 50 year old intensewildfire and subsequent regeneration at Acadia National Park(ANP), and a 17 year old whole-tree harvest at the Weymouth PointWatershed (WPW). At each site, mineral soils were sampled byuniform depth increments. Mineral soil (< 2 mm) was separatedinto light, occluded light, and heavy density fractions byfloatation in NaI solution (1.7 g cm-3). Mineral soil (< 2mm) was also separated into particle-size fractions of sand (2.0to 0.05 mm), silt (0.05 to 0.002 mm), and clay (< 0.002 mm) bywet sieving and centrifugation. Whole soils, and density andparticle-size fractions were analyzed for total C and N. Bothfractionation schemes showed that all soil organic matterfractions had lower C/N ratios as a result of N enrichment atBBWM. At ANP, soil organic matter fractions generally had lowerC/N associated with the wildfire and subsequent shift fromsoftwood to hardwood regeneration. Few significant whole soiland soil organic matter fraction differences were associated withthe whole-tree harvest. Within watershed pairs, both density andparticle-size fractionation techniques usually indicated similarresponses. Soil organic matter fractionation results indicatedthat there were no consistent shifts in fraction distributions inresponse to perturbation that were consistent across all pairedwatershed study sites.  相似文献   

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