Organic matter in density fractions of water-stable aggregates in silty soils: Effect of land use

The location of soil organic matter (SOM) within the soil matrix is considered a major factor determining its turnover, but quantitative information about the effects of land cover and land use on the distribution of SOM at the soil aggregate level is rare. We analyzed the effect of land cover/land use (spruce forest, grassland, wheat and maize) on the distribution of free particulate organic matter (POM) with a density <1.6 g cm⁻³ (free POM_<1.6), occluded particulate organic matter with densities <1.6 g cm⁻³ (occluded POM_<1.6) and 1.6-2.0 g cm⁻³ (occluded POM_1.6-2.0) and mineral-associated SOM (>2.0 g cm⁻³) in size classes of slaking-resistant aggregates (53-250, 250-1000, 1000-2000, >2000 μm) and in the sieve fraction <53 μm from silty soils by applying a combined aggregate size and density fractionation procedure. We also determined the turnover time of soil organic carbon (SOC) fractions at the aggregate level in the soil of the maize site using the ¹³C/¹²C isotope ratio. SOM contents were higher in the grassland soil aggregates than in those of the arable soils mainly because of greater contents of mineral-associated SOM. The contribution of occluded POM to total SOC in the A horizon aggregates was greater in the spruce soil (23-44%) than in the grassland (11%) and arable soils (19%). The mass and carbon content of both the free and occluded POM fractions were greater in the forest soil than in the grassland and arable soils. In all soils, the C/N ratios of soil fractions within each aggregate size class decreased in the following order: free POM_<1.6>occluded POM_<1.6-2.0>mineral-associated SOM. The mean age of SOC associated with the <53 μm mineral fraction of water-stable aggregates in the Ap horizon of the maize site varied between 63 and 69 yr in aggregates >250 μm, 76 yr in the 53-250 μm aggregate class, and 102 yr in the sieve fraction <53 μm. The mean age of SOC in the occluded POM increased with decreasing aggregate size from 20 to 30 yr in aggregates >1000 μm to 66 yr in aggregates <53 μm. Free POM had the most rapid rates of C-turnover, with residence times ranging from 10 yr in the fraction >2000 μm to 42 yr in the fraction 53-250 μm. Results indicated that SOM in slaking-resistant aggregates was not a homogeneous pool, but consisted of size/density fractions exhibiting different composition and stability. The properties of these fractions were influenced by the aggregate size. Land cover/land use were important factors controlling the amount and composition of SOM fractions at the aggregate level.     

Modeling vertical movement of organic matter in a soil incubated for 41 years with C labeled straw

The distribution of organic matter (OM) in the soil profile reflects the balance between inputs and decomposition at different depths as well as transport of OM within the profile. In this study we modeled movement of OM in the soil profile as a result of mechanisms resulting in dispersive and advective movement. The model was used to interpret the distribution of ¹⁴C in the soil profile 41 years after the labeling event. The model fitted the observed distribution of ¹⁴C well (R²=0.988, AIC_c=−82.6), with a dispersion constant of D=0.71 cm² yr⁻¹ and an advection constant of v=0.0081 cm yr⁻¹. However, the model consistently underestimated the amount of OM in the soil layers from 27 to 37 cm depth. A possible explanation for this is that different fractions of OM are transported by different mechanisms. For example, particulate OM, organomineral colloids and dissolved OM are not likely to be transported by the same mechanisms. A model with two OM fractions, one moving exclusively by dispersive processes (D=0.26 cm² yr⁻¹) and another moving by both dispersive (D=0.99 cm² yr⁻¹) and advective (v=0.23 cm yr⁻¹) processes provided a slightly better fit to the data (R²=0.995, AIC_c=−83.6). More importantly, however, this model did not show the consistent underestimation from 27 to 37 cm soil depth. This corroborates the assumption that differing movement mechanisms for different OM fractions are responsible for the observed distribution of ¹⁴C in the profile. However, varying dispersion, advection, and decay of OM with depth are also possible explanations.     

Storage and dynamics of carbon and nitrogen in soil physical fractions following woody plant invasion of grassland

Woody plant invasion of grasslands is prevalent worldwide. In the Rio Grande Plains of Texas, subtropical thorn woodlands dominated by C₃ trees/shrubs have been replacing C₄ grasslands over the past 150 yr, resulting in increased soil organic carbon (SOC) storage and concomitant increases in soil total nitrogen (STN). To elucidate mechanisms of change in SOC and STN, we separated soil organic matter into specific size/density fractions and determined the concentration of C and N in these fractions. Soils were collected from remnant grasslands (Time 0) and woody plant stands (ages 10-130 yr). Rates of whole-soil C and N accrual in the upper 15 cm of the soil profile averaged 10-30 g C m⁻² yr⁻¹ and 1-3 g N m⁻² yr⁻¹, respectively, over the past 130 yr of woodland development. These rates of accumulation have increased soil C and N stocks in older wooded areas by 100-500% relative to remnant grasslands. Probable causes of these increased pool sizes include higher rates of organic matter production in wooded areas, greater inherent biochemical resistance of woody litter to decomposition, and protection of organic matter by stabilization within soil macro- and microaggregates. The mass proportions of the free light fraction (<1.0 g cm⁻³) and macroaggregate fraction (>250 μm) increased linearly with time following woody plant invasion of grassland. Conversely, the mass proportions of free microaggregate (53-250 μm) and free silt+clay (<53 μm) fractions decreased linearly with time after woody invasion, likely reflecting stabilization of these fractions within macroaggregate structures. Carbon and N concentrations increased in all soil fractions with time following woody invasion. Approximately half of the C and N accumulated in free particulate organic matter (POM) fractions, while the remainder accrued in stable macro- and microaggregate structures. Soil C/N ratios indicated that the organic C associated with POM and macroaggregates was of more recent origin (less decomposed) than C associated with the microaggregate and silt+clay fractions. Because grassland-to-woodland conversion has been geographically extensive in grassland ecosystems worldwide during the past century, changes in soil C and N storage and dynamics documented here could have significance for global cycles of those elements.     

Organic matter turnover in soil physical fractions following woody plant invasion of grassland: Evidence from natural C and N

Soil physical structure causes differential accessibility of soil organic carbon (SOC) to decomposer organisms and is an important determinant of SOC storage and turnover. Techniques for physical fractionation of soil organic matter in conjunction with isotopic analyses (δ¹³C, δ¹⁵N) of those soil fractions have been used previously to (a) determine where organic C is stored relative to aggregate structure, (b) identify sources of SOC, (c) quantify turnover rates of SOC in specific soil fractions, and (d) evaluate organic matter quality. We used these two complementary approaches to characterize soil C storage and dynamics in the Rio Grande Plains of southern Texas where C₃ trees/shrubs (δ¹³C=−27‰) have largely replaced C₄ grasslands (δ¹³C=−14‰) over the past 100-200 years. Using a chronosequence approach, soils were collected from remnant grasslands (Time 0) and from woody plant stands ranging in age from 10 to 130 years. We separated soil organic matter into specific size/density fractions and determined their C and N concentrations and natural δ¹³C and δ¹⁵N values. Mean residence times (MRTs) of soil fractions were calculated based on changes in their δ¹³C with time after woody encroachment. The shortest MRTs (average=30 years) were associated with all particulate organic matter (POM) fractions not protected within aggregates. Fine POM (53-250 μm) within macro- and microaggregates was relatively more protected from decay, with an average MRT of 60 years. All silt+clay fractions had the longest MRTs (average=360 years) regardless of whether they were found inside or outside of aggregate structure. δ¹⁵N values of soil physical fractions were positively correlated with MRTs of the same fractions, suggesting that higher δ¹⁵N values reflect an increased degree of humification. Increased soil C and N pools in wooded areas were due to both the retention of older C₄-derived organic matter by protection within microaggregates and association with silt+clay, and the accumulation of new C₃-derived organic matter in macroaggregates and POM fractions.     

Nitrogen mineralization and nitrogen uptake by maize as influenced by light and heavy organic matter fractions

On a sandy tropical soil, organic materials (prunings of Leucaena leucocephala, Senna siamea and maize stover) with contrasting C/N ratio (13, 18 and 56, respectively) were applied at the rate of 15 t ha^?1a^?1 in order to increase the amount of soil organic matter. Two light fractions (LF1 = LF > 2 mm and LF2 = 0.25 mm < LF < 2 mm) and the heavy fraction (HF) of the soil organic matter pool were determined by means of a combined density/particle size fractionation procedure and data obtained were related to soil nitrogen mineralization under controlled conditions and to nitrogen uptake by maize under field conditions. Under controlled conditions and when the LF1 fraction was excluded, nitrogen mineralization was found not to be correlated to total organic carbon content in the soil (R²=0.02). The R²-value of the linear regression increased considerably, when amount and C/N ratio of the LF2 fraction was taken into account in the regression analysis (R² = 0.88). Under field conditions, a multiple linear regression with amount and C/N ratio of HF, LF1 and LF2 better explained variation in crop nitrogen content and nitrogen uptake of maize (R² = 0.78 and 0.94) than a simple linear regression with total organic carbon (R² = 0.48 and 0.76). The results illustrate the importance of the two light and heavy organic matter fractions for estimating soil nitrogen mineralization. Determination of light and heavy soil organic matter fractions by density/particle size fractionation seems to be a promising tool to characterize functional pools of soil organic matter.     

Molecular composition and structure of organic matter in density fractions of soils amended with corn straw for five years

Corn straw is an important source of carbon (C),and when applied to soil,it alters the accumulation and distribution of organic C.However,the mechanistic pathways by which newly added C is stored and stabilized in soil remain a subject of interest and debate among scholars.In this study,we investigated the chemistry of organic matter in different density fractions of Haplic Cambisol (sandy clay loam) in a field experiment with corn straw at8 900 kg ha^-1year^-1under no tillag...     

Organic matter status and the size, activity and metabolic diversity of the soil microbial community in the row and inter-row of sugarcane under burning and trash retention

The concentrations of organic C, labile organic fractions and the size and activity of the microbial community were measured to a depth of 30 cm below the plant row and at distances of 30 and 60 cm into the inter-row area under sugarcane under pre-harvest burning or green cane harvesting with retention of a crop residue (trash) mulch. Total root mass was similar under burning and trashing but under trashing there was a redistribution of roots towards the surface 0-10 cm in the inter-row space as roots proliferated beneath the trash mulch. Soil organic C content decreased in response to both increasing distance from the plant row (to a depth of 20 cm) and burning rather than trashing (to a depth of 10 cm). Declines in K₂SO₄-extractable C, light fraction C, microbial biomass C, basal respiration and aggregate stability in response to distance and burning were much more marked than those for organic C and occurred to a depth of 30 cm. Bulk density was greater under burnt than trashed sugarcane and was greater in the inter-row than row, particularly under burning. Heterotrophic functional diversity (measured by analysis of catabolic response profiles to 36 substrates) was also investigated. Principal component analysis of response profiles demonstrated that soils below the row and those under trashing at 30 cm out from this row were separated from the other soils on PC1 and the sample from the inter-row centre (60 cm out) under burning was separated from the others on PC2. Catabolic evenness was least for the latter soil. It was concluded that soil in the inter-row of burnt sugarcane receives few inputs of organic matter and that conversion to green cane harvesting with retention of a trash mulch greatly improves the organic matter, microbial and physical status of the inter-row soil.     

Effective retention of litter-derived dissolved organic carbon in organic layers

This study aimed to gain insight into the generation and fate of dissolved organic carbon (DOC) in organic layers. In a Free Air CO₂ Enrichment Experiment at the alpine treeline, we estimated the contribution of ¹³C-depleted recent plant C to DOC of mor-type organic layers. In an additional laboratory soil column study with 40 leaching cycles, we traced the fate of ¹³C-labelled litter-DOC (22 and 45 mg l⁻¹) in intact Oa horizons at 2 and 15 °C. Results of the field study showed that DOC in the Oa horizon at 5 cm depth contained only 20 ± 3% of less than six-year-old C, indicating minor contributions of throughfall, root exudates, and fresh litter to leached DOC. In the soil column experiment, there was a sustained DOC leaching from native soil organic matter. Less than 10% of totally added litter-DOC was leached despite a rapid breakthrough of a bromide tracer (50 ± 7% within two days). Biodegradation contributed only partly to the DOC removal with 18-30% of added litter-DOC being mineralized in the Oa horizons at 2 and 15 °C, respectively. This was substantially less than the potential 70%-biodegradability of the litter-DOC itself, which indicates a stabilization of litter-DOC in the Oa horizon. In summary, our results give evidence on an apparent ‘exchange’ of DOC in thick organic layers with litter-DOC being retained and ‘replaced’ by ‘older’ DOC leached from the large pool of indigenous soil organic matter.     

The contribution of soil organic matter fractions to carbon and nitrogen mineralization and microbial community size and structure

The aims of this study were to: (i) assess the impact of hay and fertilizer application on organic matter (OM) fractions (dissolved organic matter (DOM), light fraction organic matter (LFOM, <1.0 g cm⁻³), heavy fraction OM (HFOM, <1.7 g cm⁻³)), carbon (C) and nitrogen (N) cycling processes and microbial community size and structure, and (ii) quantify the role of OM fractions to C and N cycling. Soil was collected in 2001 from a field experiment to which grass hay (1996) and/or fertilizer (1995 and 1999) had previously been applied. DOM-C (P<0.05) and DOM-N (P=0.07) were significantly higher in control and fertilized soil than hay and hay+fertilized soil. LFOM and HFOM C and N contents and C/N ratios were significantly (P<0.05) higher in hay+fertilized and hay amended soil than in control and fertilized soil. Potentially mineralizable-N (PMN), microbial biomass-C (MB-C), microbial biomass-N (MB-N) and microbial respiration (CO₂) were not affected by fertilizer and/or hay application. Gross N mineralization (Gross Min) and gross nitrification (Gross Nit) rates were significantly (P<0.05) higher in fertilized, hay, hay+fertilized soil than control soil. However, there was no significant difference between treatments in gross N immobilization rates. Results reported here highlight the importance of a labile fraction of the DOM pool to N and C cycling as its removal significantly (P<0.05) reduced PMN, MB-N, Gross Min and Gross Nit compared with whole soil in most or all treatments. In soil where DOM+LFOM were removed PMN was significantly (P<0.05) lower, but MB-C, Gross Min and Gross Nit was significantly (P<0.05) higher than in DOM removed soil. This suggests that LFOM plays an important role as a sink for mineral-N. Total soil phospholipid fatty acid (PLFA) concentration was significantly (P<0.05) higher in hay amended than control, fertilized and hay+fertilized soil. Principal components analysis was able to clearly discriminate between control, fertilized, hay+fertilized and hay amended soil. Soil amended with hay or fertilizer had a microbial community structure which differed from that of the control or hay+fertilized soils. Redundancy analysis with Monte Carlo permutation tests revealed that PLFA profiles were strongly correlated to differences in Gross Min, Gross Nit, MB-N, MB-C, MB-C/N ratio, total soil C and total soil C/N ratio. The results of this research suggest that changes in microbial structure are related to aspects of soil C and N pools and cycling.     

Influence of earthworm activity on aggregate-associated carbon and nitrogen dynamics differs with agroecosystem management

Earthworms are known to be important regulators of soil structure and soil organic matter (SOM) dynamics, however, quantifying their influence on carbon (C) and nitrogen (N) stabilization in agroecosystems remains a pertinent task. We manipulated population densities of the earthworm Aporrectodea rosea in three maize-tomato cropping systems [conventional (i.e., mineral fertilizer), organic (i.e., composted manure and legume cover crop), and an intermediate low-input system (i.e., alternating years of legume cover crop and mineral fertilizer)] to examine their influence on C and N incorporation into soil aggregates. Two treatments, no-earthworm versus the addition of five A. rosea adults, were established in paired microcosms using electro-shocking. A ¹³C and ¹⁵N labeled cover crop was incorporated into the soil of the organic and low-input systems, while ¹⁵N mineral fertilizer was applied in the conventional system. Soil samples were collected during the growing season and wet-sieved to obtain three aggregate size classes: macroaggregates (>250 μm), microaggregates (53-250 μm) and silt and clay fraction (<53 μm). Macroaggregates were further separated into coarse particulate organic matter (cPOM), microaggregates and the silt and clay fraction. Total C, ¹³C, total N and ¹⁵N were measured for all fractions and the bulk soil. Significant earthworm influences were restricted to the low-input and conventional systems on the final sampling date. In the low-input system, earthworms increased the incorporation of new C into microaggregates within macroaggregates by 35% (2.8 g m⁻² increase; P=0.03), compared to the no-earthworm treatment. Within this same cropping system, earthworms increased new N in the cPOM and the silt and clay fractions within macroaggregates, by 49% (0.21 g m⁻²; P<0.01) and 38% (0.19 g m⁻²; P=0.02), respectively. In the conventional system, earthworms appeared to decrease the incorporation of new N into free microaggregates and macroaggregates by 49% (1.38 g m⁻²; P=0.04) and 41% (0.51 g m⁻²; P=0.057), respectively. These results indicate that earthworms can play an important role in C and N dynamics and that agroecosystem management greatly influences the magnitude and direction of their effect.     

Soil organic matter dynamics along a rice chronosequence in north-eastern Argentina: Evidence from natural C abundance and particle size fractionation

We studied the consequences of rice cultivation and its subsequent abandonment for soil organic matter (SOM) dynamics in north-eastern Argentina. Two chronosequences, which included a pristine grassland with C4 vegetation as a control, and several stages of rice (C3) fields abandoned for 1, 2, 4, 6 and 15 years were selected, and soil samples from the first 10 cm were gathered from each plot. Natural ¹³C abundance coupled with particle-size fractionation were employed to characterize SOM changes through time discriminated by SOM origin. Soil samples up to 50 cm were also collected throughout one chronosequence. Most changes in SOM occurred on the first 20 cm layer and, bulk density, carbon and nitrogen content, as well as δ¹³C remained similar at greater depths. After the rice cropping, the bulk density was slightly greater than in the natural grassland, and remained stable after the abandonment. Carbon and nitrogen contents remained almost stable in the surface layer during the cultivation. δ¹³C varied accordingly with the changes in vegetation cover with a C4 signature in the natural grassland and mainly a C3 signature in the rice fields. The abandonment of the rice cropping induced a decrease of the soil organic matter content, mainly of natural grassland origin, during the first 4 years. When the abandonment extended, the SOM content (from C4 origin) increased slowly and after 15 years, was almost the same as that of the natural grassland. The carbon turnover was greater in the coarser fractions than in the finer ones, confirming that soil organic carbon in the sand fraction was relatively labile. However, all the fractions were affected by inputs and outputs of C derived from rice and natural grassland. This fact could indicate that the former protected carbon could become less stable due to cultivation.     

Gross N transformation rates and net N mineralisation rates related to the C and N contents of soil organic matter fractions in grassland soils of different age

We investigated the relationship between soil organic matter (SOM) content and N dynamics in three grassland soils (0-10 and 10-20 cm depth) of different age (6, 14 and 50 y-old) with sandy loam textures. To study the distribution of the total C and N content the SOM was fractionated into light, intermediate and heavy density fractions of particulate macro-organic matter (150-2000 μm) and the 50-150 μm and <50 μm size fractions. The potential gross N transformation rates (mineralisation, nitrification, NH₄⁺ and NO₃⁻ immobilization) were determined by means of short-term, fully mirrored ¹⁵N isotope dilution experiments (7-d incubations). The long-term potential net N mineralisation and gross N immobilization rates were measured in 70-d incubations. The total C and N contents mainly tended to increase in the 0-10 cm layer with increasing age of the grassland soils. Significant differences in total SOM storage were detected for the long-term (50 y-old) conversion from arable land to permanent grassland. The largest relative increase in C and N contents had occurred in the heavy density fraction of the macro-organic matter, followed by the 50-150 and <50 μm fractions. Our results suggest that the heavy density fraction of the macro-organic matter could serve as a good indicator of early SOM accumulation, induced by converting arable land to permanent grassland. Gross N mineralisation, nitrification, and (long-term) gross N immobilization rates tended to increase with increasing age of the grasslands, and showed strong, positive correlations with the total C and N contents. The calculated gross N mineralisation rates (7-d incubations) and net N mineralisation rates (70-d incubations) corresponded with a gross N mineralisation of 643, 982 and 1876 kg N ha⁻¹ y⁻¹, and a net N mineralisation of 195, 208 and 274 kg N ha⁻¹ y⁻¹ in the upper 20 cm of the 6, 14 and 50 y-old grassland soils, respectively. Linear regression analysis showed that 93% of the variability of the gross N mineralisation rates could be explained by variation in the total N contents, whereas total N contents together with the C-to-N ratios of the <50 μm fraction explained 84% of the variability of the net N mineralisation rates. The relationship between long-term net N mineralisation rates and gross N mineralisation rates could be fitted by means of a logarithmic equation (net m=0.24Ln(gross m)+0.23, R²=0.69, P<0.05), which reflects that the ratio of gross N immobilization-to-gross N mineralisation tended to increase with increasing SOM contents. Microbial demand for N tended to increase with increasing SOM content in the grassland soils, indicating that potential N retention in soils through microbial N immobilization tends to be limited by C availability.     

Increased N deposition retards mineralization of old soil organic matter

The aim of this study was to investigate the effects of increased N deposition on new and old pools of soil organic matter (SOM). We made use of a 4-yr experiment, where spruce and beech growing on an acidic loam and a calcareous sand were exposed to increased N deposition (7 vs. 70 kg N ha⁻¹ yr⁻¹) and to elevated atmospheric CO₂. The added CO₂ was depleted in ¹³C, which enabled us to distinguish between old and new C in SOM-pools fractionated into particle sizes. Elevated N deposition for 4 yr increased significantly the contents of total SOM in 0-10 cm depth of the acidic loam (+9%), but not in the calcareous sand. Down to 25 cm soil depth, C storage in the acidic loam was between 100 and 300 g C m⁻² larger under high than under low N additions. However, this increase was small as compared with the SOM losses of 600-700 g C g C 0.25 m⁻¹ m⁻² from the calcareous sand resulting from the disturbance of soils during setting up of the experiment. The amounts of new, less than 4 yr old SOM in the sand fractions of both soils were greater under high N deposition, showing that C inputs from trees into soils increased. Root biomass in the acidic loam was larger under N additions (+25%). Contents of old, more than 4 yr old C in the clay and silt fractions of both soils were significantly greater under high than under low N deposition. Since clay- and silt-bound SOM consists of humified compounds, this indicates that N additions retarded mineralization of old and humified SOM. The retardation of C mineralization in the clay and silt fraction accounted for 60-80 g C m⁻² 4 yr⁻¹, which corresponds to about 40% of the old SOM mineralized in these fraction. As a consequence, preservation of old and humified SOM under elevated N deposition might be a process that could lead to an increased soil C storage in the long-term.     

Qualitative and quantitative differences in particulate organic matter fractions in organic and conventional farming systems

To quantify functionally important differences in soil organic matter (SOM) that result from use of different farming practices, soils from 9 long-term trials comparing manure+legume-based organic, legume-based organic, and conventional farming systems were collected and particulate organic matter (POM) was fractionated to reflect its position within the soil matrix. The free, light POM (FPOM; <1.6 g cm⁻³) not occluded within aggregates and occluded POM (OPOM; <2.0 g cm⁻³) were compared to an undifferentiated POM fraction (coarse fraction, CF; >53 μm) obtained by wet sieving. Fraction C, N, and hydrolyzable N (quantified using the Illinois test (IL-N)) were determined. Organic farming systems had greater quantities of C and N in the OPOM and CF and, greater IL-N contents in all POM fractions considered. The OPOM's C:N ratio (16-19) and was least in the manure+legume-based organic, intermediate in the legume-based organic, and greatest in the conventional systems (P<0.10). Trends in OPOM C:N and IL-N abundance suggested occluded POM was most decomposed, and possibly a greater N reservoir, in the manured soils. The FPOM quality reflected the residues added to each system and its removal improved resolution of quality-based differences in POM associated with long-term management. Subdivision of POM revealed differences in its quality that were not evident using the undifferentiated CF. Quantification of hydrolysable N (IL-N) in POM did not enhance our understanding of management's affect on SOM quality. This multi-site comparison showed organic management simultaneously increased the size of the labile N reservoir and the amount of POM protected within aggregates; and that, occluded POM is more decomposed in manure+legume- than in legume-based organic systems. The characteristics of POM reveal how organic practices improve SOM and suggest the nutrient and substrate decay dynamics of organic systems may differ as a result of the N fertilization strategies they employ.     

Variability in soil properties at different spatial scales (1 m-1 km) in a deciduous forest ecosystem

The purpose of this research was to test the hypothesis that variability in 11 soil properties, related to soil texture and soil C and N, would increase from small (1 m) to large (1 km) spatial scales in a temperate, mixed-hardwood forest ecosystem in east Tennessee, USA. The results were somewhat surprising and indicated that a fundamental assumption in geospatial analysis, namely that variability increases with increasing spatial scale, did not apply for at least five of the 11 soil properties measured over a 0.5-km² area. Composite mineral soil samples (15 cm deep) were collected at 1, 5, 10, 50, 250, and 500 m distances from a center point along transects in a north, south, east, and westerly direction. A null hypothesis of equal variance at different spatial scales was rejected (P?0.05) for mineral soil C concentration, silt content, and the C-to-N ratios in particulate organic matter (POM), mineral-associated organic matter (MOM), and whole surface soil. Results from different tests of spatial variation, based on coefficients of variation or a Mantel test, led to similar conclusions about measurement variability and geographic distance for eight of the 11 variables examined. Measurements of mineral soil C and N concentrations, C concentrations in MOM, extractable soil NH₄-N, and clay contents were just as variable at smaller scales (1-10 m) as they were at larger scales (50-500 m). On the other hand, measurement variation in mineral soil C-to-N ratios, MOM C-to-N ratios, and the fraction of soil C in POM clearly increased from smaller to larger spatial scales. With the exception of extractable soil NH₄-N, measured soil properties in the forest ecosystem could be estimated (with 95% confidence) to within 15% of their true mean with a relatively modest number of sampling points (n?25). For some variables, scaling up variation from smaller to larger spatial domains within the ecosystem could be relatively easy because small-scale variation may be indicative of variation at larger scales.     

Stabilization of organic matter by soil minerals — investigations of density and particle‐size fractions from two acid forest soils

We tested the hypothesis whether organic matter in subsoils is a large contributor to organic carbon (OC) in terrestrial ecosystems and if survival of organic matter in subsoils is the result of an association with the soil mineral matrix. We approached this by analyzing two forest soil profiles, a Haplic Podzol and a Dystric Cambisol, for the depth distribution of OC, its distribution among density and particle‐size fractions, and the extractability of OC after destruction of the mineral phase by treatment with hydrofluoric acid (HF). The results were related to indicators of the soil mineralogy and the specific surface area. Finally, scanning electron microscopy combined with energy dispersive X‐ray spectroscopy (SEM‐EDX) was used to visualize the location of OC at mineral surfaces and associations with elements of mineral phases. The subsoils (B and C horizons) contained 40—50% of the soil OC including the organic forest floor layers. With increasing depth of soil profiles (1) the radiocarbon ages increased, and (2) increasing portions of OC were either HF‐soluble, or located in the density fraction d >1.6 g cm^—3, or in the clay fraction. The proportions of OC in the density fraction d >1.6 g cm^—3 were closely correlated to the contents of oxalate and dithionite‐citrate‐bicarbonate‐extractable Fe (r² = 0.93 and 0.88, P <0.001). SEM‐EDX analyses suggested associations of OC with aluminum whereas silicon‐enriched regions were poor in OC. The specific surface area and the microporosity of the soil mineral matrix after destruction of organic matter were less closely correlated to OC than the extractable iron fractions. This is possibly due to variable surface loadings, depending on different OC inputs with depth. Our results imply that subsoils are important for the storage of OC in terrestrial ecosystems because of intimate association of organic matter with secondary hydrous aluminum and iron phases leading to stabilization against biological degradation.     

Soil organic matter dynamics and land use change at a grassland/forest ecotone

In the grassland/forest ecotone of North America, many areas are experiencing afforestation and subsequent shifts in ecosystem carbon (C) stocks. Ecosystem scientists commonly employ a suite of techniques to examine how such land use changes can impact soil organic matter (SOM) forms and dynamics. This study employs four such techniques to compare SOM in grassland (Bromus inermis) and recently forested (∼35 year, Ulmus spp. and Quercus spp.) sites with similar soil types and long-term histories in Kansas, USA. The work examines C and nitrogen (N) parameters in labile and recalcitrant SOM fractions isolated via size and density fractionation, acid hydrolysis, and long-term incubations. Size fractionation highlighted differences between grassland and forested areas. N concentration of forested soils’ 63-212 μm fraction was higher than corresponding grassland soils’ values (3.0±0.3 vs. 2.3±0.3 mg g_fraction⁻¹, P<0.05), and N concentration of grassland soils’ 212-2000 μm fraction was higher than forested soils (3.0±0.4 vs. 2.3±0.2 mg g_fraction⁻¹, P<0.05). Similar trends were observed for these same fractions for C concentration; forested soils exhibited 1.3 times the C concentration in the 63-212 μm fraction compared to this fraction in grassland soils. Fractions separated via density separation and acid hydrolysis exhibited no differences in [C], [N], δ¹⁵N, or δ¹³C when compared across land use types. Plant litterfall from forested sites possessed significantly greater N concentrations than that from grassland sites (12.41±0.10 vs. 11.62±0.19 mg g_litter⁻¹). Long-term incubations revealed no differences in C or N dynamics between grassland and forested soils. δ¹³C and δ¹⁵N values of the smallest size and the heavier density fractions, likely representing older and more recalcitrant SOM, were enriched compared to younger and more labile SOM fractions; δ¹⁵N of forested soils’ 212-2000 μm fraction were higher than corresponding grassland soils (1.7±0.3‰ vs. 0.5±0.4‰). δ¹³C values of acid hydrolysis fractions likely reflect preferential losses of ¹³C-depleted compounds during hydrolysis. Though C and N data from size fractions were most effective at exhibiting differences between grassland and forested soils, no technique conclusively indicates consistent changes in SOM dynamics with forest growth on these soils. The study also highlights some of the challenges associated with describing SOM parameters, particularly δ¹³C, in SOM fractions isolated by acid hydrolysis.     

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 nitrogenous N-containing 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 other organics could sorb more readily than onto the unconditioned 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⁻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 ¹⁴C mean residence time (MRT) increased with particle density from ca. 150 years to >980 years in the four organo-mineral fractions. In contrast, C/N, ¹³C and ¹⁵N 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 (SDF) 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 SDF isolated pools of distinct mineralogy and organic-matter composition, more work will be needed to understand mechanisms relating the two factors.     

Effects of past, present and future atmospheric CO2 concentrations on soil organic matter dynamics in a chaparral ecosystem

Owing to the continuously increasing concentration of atmospheric CO₂, it has become a priority to understand if soil organic matter (SOM) will behave as a sink or a source of CO₂ under future environmental changes. Although many studies have addressed this question, a clear understanding is still missing, particularly with respect to long-term responses. In this study, we quantified soil C stores and dynamics in relationship to soil aggregation and pool composition in a Californian chaparral ecosystem exposed for 6 years to a gradient of atmospheric CO₂ concentrations, ranging from pre-industrial levels 250 to 750 μl l⁻¹ CO₂. Fossil fuel-derived CO₂ depleted in ¹³C was used for the fumigation, thus providing a tracer of C input from the vegetation to the soil.Long-term CO₂ exposure invariably affected soil aggregation, with a significant decrease in the macroaggregate fraction at highest CO₂ levels relative to the other two size fractions (i.e. microaggregates and silt and clay). This soil structural change most likely reduced the stability and protection of SOM, and C content generally decreased in most fractions over the CO₂ treatments, and induced faster turnover of recently fixed C at high CO₂ levels. The strongest response was found in the C content of the microaggregates, which decreased significantly (P<0.05) with rising levels of CO₂. We conclude that increasing atmospheric CO₂ concentrations will decrease soil C in chaparral ecosystems, and that the microaggregate fraction is the most responsive to increasing concentrations of atmospheric CO₂.