Chemical composition of organic matter in a deep soil changed with a positive priming effect due to glucose addition as investigated by 13C NMR spectroscopy

Fresh organic carbon becomes more accessible to deep soil following losses of surface soil and deep intentional incorporation of crop residues, which can cause the priming effect and influence the quality and quantity of SOC in deep soil. This study determined the priming effect due to addition of water-dissolved ¹³C-labeled glucose (0.4 g C kg⁻¹ soil) to a soil taken from 1.00 to 1.20 m depth. The changes in chemical compositions of SOC in soils without (G₀) and with (G_0.4) glucose addition during a 31-d incubation were investigated with solid-state ¹³C cross polarization/total sideband suppression (¹³C-CP/TOSS) and CP/TOSS with dipolar dephasing nuclear magnetic resonance (NMR) techniques. No glucose remained in the soil after 21 days of incubation, with 48% being completely mineralized into CO₂ emission and 52% being incorporated into SOC. The native SOC was decomposed by 0.23% more in G_0.4 than in G₀. The NMR spectra demonstrated that both labile and recalcitrant organic compounds in SOC changed during the incubation, but in different manners in G₀ and G_0.4. During the incubation, the -(CH₂)_n-abundance in G₀ did not change over time, but in G_0.4 it decreased from Day 0 to Day 21 and then increased from Day 21 to Day 31, suggesting shifts of soil microbial communities only in G_0.4. After the incubation, in G₀ the abundances of ketones/aldehydes and nonpolar alkyl C increased, but those of aromatic C–C and protonated O-alkyl C (OCH) decreased; In G_0.4, the abundances of NCH and protonated O-alkyl C (OCH) increased, but those of nonpolar alkyl C and nonprotonated aromatic C–O and ketones/aldehydes decreased. Such inconsistent changes in recalcitrant compounds between G₀ and G_0.4 indicated that glucose addition likely primed the decomposition of aromatic C–O and suppressed the formation of ketones/aldehydes. We have demonstrated for the first time that the priming effect of SOC decomposition in the deep soil was involved with larger notable changes in both labile and recalcitrant structures of native SOC due to glucose addition compared with that without glucose addition.     

Drying and rewetting effects on C and N mineralization and microbial activity in surface and subsurface California grassland soils

Rewetting a dry soil has long been known to cause a burst of respiration (the “Birch Effect”). Hypothesized mechanisms for this involve: (1) release of cellular materials as a result of the rapid increase in water potential stress and (2) stimulating C-supply to microbes via physical processes. The balance of these factors is still not well understood, particularly in the contexts of multiple dry/wet cycles and of how resource and stress patterns vary through the soil profile. We evaluated the effects of multiple dry/wet cycles on surface and subsurface soils from a California annual grassland. Treatments included 4, 6, and 12 cycles that varied the length of the drying period between rewetting events. Respiration was monitored after each wetting event while extractable C and N, microbial biomass, and microbial activity were assayed initially, after the first rewetting event, and at the end of the experiment. Initially, microbial biomass and activity (respiration, dehydrogenase, and N mineralization) in subsurface soils were ca. 10% and 20% of surface soil levels. After multiple cycles, however, subsurface soil microbial biomass and activity were enhanced by up to 8-fold, even in comparison to the constantly moist treatment. By comparison, surface soil microbial biomass and activity were either moderately (i.e. 1.5 times increase) or not affected by wetting and drying. Drying and rewetting led to a cascade of responses (soluble C release, biomass growth, and enhanced activity) that mobilized and metabolized otherwise unavailable soil carbon, particularly in subsurface soils.     

Effects of soil texture and structure on carbon and nitrogen mineralization in grassland soils

Summary The hypotheses that disruption of soil structure increases mineralization rates in loams and clays more than in sandy soils and that this increase can be used to estimate the fraction of physically protected organic matter were tested. C and N mineralization was measured in undisturbed, and in finely and coarsely sieved moist or dried/remoistened soil. Fine sieving caused a temporary increase in mineralization. The relative increase in mineralization was much larger in loams and clays than in sandy soils and much larger for N than for C. The combination of remoistening and sieving of the soil gave a further increase in the mineralization flush after the disturbance. Again, the extra flush was larger in loams and clays than in sandy soils, and larger for N than for C. In loams and clays, small pores constituted a higher percentage of the total pore space than in sandy soils. The fraction of small pores explained more than 50% of the variation in the N mineralization rate between soils. There was also a good correlation between the small-pore fraction and the relative increase in N mineralization with fine sieving. For C, these relations were not clear. It is suggested that a large part of the organic matter that was present in the small pores could not be reached by microorganisms, and was therefore physically protected against decomposition. Fine sieving exposed part of this fraction to decomposition. This physically protected organic matter had a lower C: N ratio than the rest of the soil organic matter. The increase in N mineralization after fine sieving can be regarded as a measure of physically protected organic matter.     

Positive and negative carbon mineralization priming effects among a variety of biochar-amended soils

Pyrogenic carbon (biochar) amendment is increasingly discussed as a method to increase soil fertility while sequestering atmospheric carbon (C). However, both increased and decreased C mineralization has been observed following biochar additions to soils. In an effort to better understand the interaction of pyrogenic C and soil organic matter (OM), a range of Florida soils were incubated with a range of laboratory-produced biochars and CO₂ evolution was measured over more than one year. More C was released from biochar-amended than from non-amended soils and cumulative mineralized C generally increased with decreasing biomass combustion temperature and from hardwood to grass biochars, similar to the pattern of biochar lability previously determined from separate incubations of biochar alone.The interactive effects of biochar addition to soil on CO₂ evolution (priming) were evaluated by comparing the additive CO₂ release expected from separate incubations of soil and biochar with that actually measured from corresponding biochar and soil mixtures. Priming direction (positive or negative for C mineralization stimulation or suppression, respectively) and magnitude varied with soil and biochar type, ranging from −52 to 89% at the end of 1 year. In general, C mineralization was greater than expected (positive priming) for soils combined with biochars produced at low temperatures (250 and 400 °C) and from grasses, particularly during the early incubation stage (first 90 d) and in soils of lower organic C content. It contrast, C mineralization was generally less than expected (negative priming) for soils combined with biochars produced at high temperatures (525 and 650 °C) and from hard woods, particularly during the later incubation stage (250-500 d). Measurements of the stable isotopic signature of respired CO₂ indicated that, for grass biochars at least, it was predominantly pyrogenic C mineralization that was stimulated during early incubation and soil C mineralization that was suppressed during later incubation stages. It is hypothesized that the presence of soil OM stimulated the co-mineralization of the more labile components of biochar over the short term. The data strongly suggests, however, that over the long term, biochar-soil interaction will enhance soil C storage via the processes of OM sorption to biochar and physical protection.     

Activities of extracellular enzymes in physically isolated fractions of restored grassland soils

Extracellular enzymes degrade complex organic compounds and contribute to carbon turnover in soils. We used physical fractionation procedures to investigate whether soil carbon is spatially isolated from degradative enzymes across a prairie restoration chronosequence in Illinois, USA. We found that carbon-degrading enzymes were abundant in all soil fractions, including macroaggregates, microaggregates, and the clay-sized fraction. The activities of two cellulose-degrading enzymes and a chitin-degrading enzyme were 2-10 times greater in particulate organic matter (POM) fractions than in bulk soil, consistent with the rapid turnover of POM fractions. Polyphenol oxidase activity in the clay-sized fraction was 3 times that in the bulk soil, despite a higher mean residence time for carbon in the clay-sized fraction. For most enzymes, differences in activity among fractions and across the restoration chronosequence diminished when adjusted for differences in carbon concentrations. However, glycine aminopeptidase activity per unit carbon increased four-fold across the chronosequence in the clay fraction, while polyphenol oxidase activity declined by 40%. These results suggest that enzyme production and carbon turnover occur rapidly in POM fractions, but slowly in mineral-dominated fractions where enzymes and their carbon substrates are immobilized on mineral surfaces. Soil carbon accumulation in mineral fractions and across the prairie restoration chronosequence probably reflects increasing physical isolation of enzymes and substrates on the molecular to micron scale, rather than exclusion of enzymes from entire soil fractions. Based on these mechanisms, land managers could increase soil C stocks by reducing the physical disruption of soil structure associated with cultivation.     

The proportional mineralisation of microbial biomass and organic matter caused by air-drying and rewetting of a grassland soil

During the first few days after rewetting of an air-dried soil (AD-RW), microbial activity increases compared to that in the original moist soil, causing increased mineralisation (a flush) of soil organic carbon (C) and other nutrients. The AD-RW flush is believed to be derived from the enhanced mineralisation of both non-biomass soil organic matter (due to its physical release and enhanced availability) and microbial biomass killed during drying and rewetting. Our aim was to determine the effects of AD-RW on the mineralisation of soil organic matter and microbial biomass during and after repeated AD-RW cycles and to quantify their proportions in the CO₂-C flushes that resulted. To do this, a UK grassland soil was amended with ¹⁴C-labelled glucose to label the biomass and then given five AD-RW cycles, each followed by 7 d incubation at 25 °C and 50% water holding capacity. Each AD-RW cycle increased the amount of CO₂-C evolved (varying from 83 to 240 μg g⁻¹ soil), compared to the control with, overall, less CO₂-C being evolved as the number of AD-RW cycles increased. In the first cycle, the amount of biomass C decreased by 44% and microbial ATP by 70% while concentrations of extractable C nearly doubled. However, all rapidly recovered and within 1.3 d after rewetting, biomass C was 87% and ATP was 78% of the initial concentrations measured prior to air-drying. Similarly, by 2 d, extractable organic C had decreased to a similar concentration to the original. After the five AD-RW cycles, the amounts of total and ¹⁴C-labelled biomass C remaining in the soil accounted for 60 and 40% of those in the similarly incubated control soil, respectively. Soil biomass ATP concentrations following the first AD-RW cycle remained remarkably constant (ranging from about 10 to 14 μmol ATP g⁻¹ biomass C) and very similar to the concentration in the fresh soil prior to air-drying. We developed a simple mathematical procedure to estimate the proportion of CO₂-C derived from biomass C and non-biomass C during AD-RW. From it, we estimate that, over the five AD-RW cycles, about 60% of the CO₂-C evolved came from mineralisation of non-biomass organic C and the remainder from the biomass C itself.     

Differentiating sources of CO2 from organic soil under bioenergy crop cultivation: A field-based approach using C

We tested here a plant-soil system to separate recent, plant-derived and native, soil-derived carbon in soil respiration. The approach uses a perennial crop cultivated on an organic soil where upper soil layers have been removed as a result of peat extraction. There, the ¹⁴C signal from native organic matter is highly depleted compared to that in vegetation established at the site after peat extraction ceased. Radiocarbon was analyzed in carbon dioxide respired from soil over one growing season, and a two-pool isotope mixing model was applied to calculate the relative contribution of old vs. new carbon sources. The analysis showed that the approach is reliable for source partitioning with isotopes. After six years of cultivation, old peat decomposition contributed less to total soil respiration than respiration of recent plant material (30% vs. 70% on average, respectively), but the relative proportions were highly variable over the growing season. The approach offers a new possibility to follow the fate of old, native soil organic matter in highly organic soils.     

Cation exchange capacity of density fractions from paired conifer/grassland soils

The cation exchange capacity (CEC) of a soil depends on the type and amount of both mineral and organic surfaces. Previous studies that have sought to determine the relative contribution of organic matter to total soil CEC have not addressed differences in soil organic matter (SOM) composition that could lead to differences in CEC. The objectives of this study were (1) to compare the CEC of two distinct SOM pools, the “light fraction (LF)” composed of particulate plant, animal, and microbial debris, and the “heavy fraction (HF)” composed of mineral-bound organic matter; and (2) to examine the effects of differences in aboveground vegetation on CEC. Soil samples were collected from four paired grassland/conifer sites within a single forested area and density fractionated. LF CEC was higher in conifer soils than in grassland soils, but there was no evidence of an effect of vegetation on CEC for the HF or bulk soil. LF CEC (but not HF CEC) correlated well with the C concentration in the fraction. The mean CEC of both fractions (per kg fraction) exceeded that of the bulk soil; thus, when the LF and HF CEC were combined mathematically by weighting values for each fraction in proportion to dry mass, the resulting value was nearly twice the measured CEC of bulk soil. On a whole soil basis, the HF contributed on average 97% of the CEC of the whole soil, although this conclusion must be tempered given the inflation of CEC values by the density fractionation procedure.     

Physical protection of mineralizable C in aggregates from long-term pasture and arable soil

Depending on agricultural management, soil aggregation can provide physical protection of organic matter against rapid decomposition. Within a given soil series, farm management affects the quality and quantity of organic inputs, soil disturbance and biological activity, and thereby the processes of aggregate formation (biogenic vs. physicogenic). We determined the physical protection of readily mineralizable organic matter against mineralization in undisturbed aggregates from a conventional arable field and a permanent pasture (>70 years). Soil samples from the two fields were incubated at constant temperature and moisture content, corresponding to field capacity. The increase in CO₂ evolution due to crushing (<250 μm) of the aggregates was used to estimate the macroaggregate-protected C fraction. The fraction of C protected at the microstructural level was estimated from the increase in CO₂ evolution after ball-mill grinding. In addition, aggregate size distribution and bulk density and porosity of undisturbed soil and macroaggregates were determined. Unprotected C fractions were not significantly different between the management systems and ranged from 1.9% to 2.4% of total organic C. In the arable soil, 1.4% of total soil organic C was physically protected in macroaggregates. Crushing of macroaggregates did not significantly increase C mineralization in the pasture soil. The results indicate that mineralization was considerably suppressed in the dominantly large and dense physicogenic macroaggregates from the arable field, but not in the dominantly porous, biogenic macroaggregates of the pasture soil. However, the protection in macroaggregates from the arable soil is not likely to be effective on the long-term because of the low water stability and the disrupting forces of cultivation under field conditions. A relatively high additional C mineralization from ground compared to crushed soil material, especially in the upper layer of the pasture soil, suggests a more important C protection at the microstructural level. Higher C protection in microaggregates from the pasture soil was supported by a previous micromorphological study of soil microstructures in thin sections of the considered management systems.     

Contribution of sorption,DOC transport and microbial interactions to the 14C age of a soil organic carbon profile: Insights from a calibrated process model

Profiles of soil organic carbon (SOC) are often characterized by a steep increase of ¹⁴C age with depth, often leading to subsoil ¹⁴C ages of more than 1000 years. These observations have generally been reproduced in SOC models by introducing a SOC pool that decomposes on the time-scale of millennia. The overemphasis of chemical recalcitrance as the major factor for the persistence of SOC was able to provide a mechanistic justification for these very low decomposition rates. The emerging view on SOC persistence, however, stresses that apart from molecular structure a multitude of mechanisms can lead to the long-term persistence of organic carbon in soils. These mechanisms, however, have not been incorporated into most models. Consequently, we developed the SOC profile model COMISSION which simulates vertically resolved SOC concentrations based on representations of microbial interactions, sorption to minerals, and vertical transport. We calibrated COMISSION using published concentrations of SOC, microbial biomass and mineral-associated OC (MOC), and in addition, ¹⁴C contents of SOC and MOC of a Haplic Podzol profile in North-Eastern Bavaria, Germany. In order to elucidate the contribution of the implemented processes to the ¹⁴C age in different parts of the profile, we performed model-experiments in which we switched off the limitation of SOC decomposition by microbes, sorptive stabilization on soil minerals, and dissolved OC (DOC) transport. By splitting all model pools into directly litter-derived carbon and microbe-derived organic carbon, we investigated the contribution of repeated microbial recycling to ¹⁴C ages throughout the profile. The model-experiments for this site lead to the following implications: Without rejuvenation by DOC transport, SOC in the subsoil would be on average 1700 ¹⁴C years older. Across the profile, SOC from microbial recycling is on average 1400 ¹⁴C years older than litter-derived SOC. Without microbial limitation of depolymerization, SOC in the subsoil would be on average 610 ¹⁴C years younger. Sorptive stabilization is responsible for relatively high ¹⁴C ages in the topsoil. The model-experiments further indicate that the high SOC concentrations in the Bh horizon are caused by the interplay between sorptive stabilization and microbial dynamics. Overall, the model-experiments demonstrate that the high ¹⁴C ages are not solely caused by slow turnover of a single pool, but that the increase of ¹⁴C ages along a soil profile up to ages >1000 years is the result of different mechanisms contributing to the overall persistence of SOC. The dominant reasons for the persistence of SOC are stabilization processes, followed by repeated microbial processing of SOC.     

CO2 emissions from subtropical arable soils of China

CO₂ efflux plays a key role in carbon exchange between the biosphere and atmosphere, but our understanding of the mechanism controlling its temporal and spatial variations is limited. The purpose of this study is to determine annual soil CO₂ flux and assess its variations in arable subtropical soils of China in relation to soil temperature, moisture, rainfall, microbial biomass carbon (MBC) and dissolved organic carbon (DOC) using the closed chamber method. Soils were derived from three parent materials including granite (G), tertiary red sandstone (T) and quaternary red clay (Q). The experiment was conducted at the Ecological Station of Red Soil, The Chinese Academy of Sciences, in a subtropical region of China. The results showed that soil CO₂ flux had clear seasonal fluctuations with the maximum value in summer, the minimum in winter and intermediate in spring and autumn. Further, significant differences in soil CO₂ flux were found among the three red soils, generally in the order of G>T>Q. The average annual fluxes were estimated as 2.84, 2.13 and 1.41 kg CO₂ m⁻² year⁻¹ for red soils derived from G, T and Q, respectively. Soil temperature strongly affects the seasonal variability of soil CO₂ flux (85.0-88.5% of the variability), followed by DOC (55.8-84.4%) and rainfall (43.0-55.8%). The differences in soil CO₂ flux among the three red soils were partly explained by MBC (33.7-58.9% of the variability) and DOC (23.8-33.6%).     

Organic C levels in intensively managed arable soils – long-term regional trends and characterization of fractions

Substantial losses of soil organic carbon (SOC) from the plough layer of intensively managed arable soils in western Europe have recently been reported, but these estimates are associated with very large uncertainties. Following soil surveys in 1952 and 1990 of arable soils in West Flanders (Belgium), we resampled 116 sites in 2003 and thus obtained three paired measurements of the OC stocks in these soils. Ten soils were selected for detailed physical fractionation to obtain possible further explanations for changes in SOC stocks. Between 1990 and 2003, the SOC stocks decreased at an average rate of ?0.19 t OC ha^?1 year^?1. This loss is significant but is still less than half the rate of SOC decrease that was estimated previously for the whole region of Flanders, which includes the study area. Variation in SOC stocks or in the magnitude of SOC stock losses could not be related to soil texture, to changes in ploughing depth, or to recent land‐use changes. A good relationship, however, was found between the SOC losses and organic matter (OM) inputs. The results of the physical fractionation also suggested management to be the predominant factor determining variation in SOC stocks because no correlation was found between soil texture and the absolute amounts of OC present in the largest OM fractions, that is, the OC in free particulate organic matter (POM), and OC associated with the silt + clay size fraction. The proportion of OC in free POM was up to 40% of the total OC, which indicates the important impact of management on SOC and also indicates that a substantial part of the SOC still present, may in the future be lost at a time scale of years to decades assuming that the intensive management continues.     

Isotope (C and C) analysis of deep peat CO2 using a passive sampling technique

We developed and tested a new method to collect CO₂ from the surface to deep layers of a peatland for radiocarbon analysis. The method comprises two components: i) a probe equipped with a hydrophobic filter that allows entry of peat gases by diffusion, whilst simultaneously excluding water, and, ii) a cartridge containing zeolite molecular sieve that traps CO₂ passively. We field tested the method by sampling at depths of between 0.25 and 4 m at duplicate sites within a temperate raised peat bog. CO₂ was trapped at a depth-dependent rate of between ∼0.2 and 0.8 ml d⁻¹, enabling sufficient CO₂ for routine ¹⁴C analysis to be collected when left in place for several weeks. The age of peatland CO₂ increased with depth from modern to ∼170 BP for samples collected from 0.25 m, to ∼4000 BP at 4 m. The CO₂ was younger, but followed a similar trend to the age profile of bulk peat previously reported for the site (Langdon and Barber, 2005). δ¹³C values of recovered CO₂ increased with depth. CO₂ collected from the deepest sampling probes was considerably ¹³C-enriched (up to ∼+9‰) and agreed well with results reported for other peatlands where this phenomenon has been attributed to fermentation processes. CO₂ collected from plant-free static chambers at the surface of the mire was slightly ¹⁴C-enriched compared to the contemporary atmosphere, suggesting that surface CO₂ emissions were predominantly derived from carbon fixed during the post-bomb era. However, consistent trends of enriched ¹³C and depleted ¹⁴C in chamber CO₂ between autumn and winter samples were most likely explained by an increased contribution of deep peat CO₂ to the surface efflux in winter. The passive sampling technique is readily portable, easy to install and operate, causes minimal site disturbance, and can be reliably used to collect peatland CO₂ from a wide range of depths.     

Effect of dry-wet cycles on carbon dioxide release from two different volcanic ash soils in a Japanese temperate forest

ABSTRACT

In the present study, two volcanic ash soils (soil A and B) from a temperate broad-leaved forest in eastern Japan were aerobically incubated under repeated dry-wet cycles and continuously constant moisture conditions. The primary aims were to quantify the potential for enhancement of carbon dioxide (CO₂) release owing to increased water fluctuation and to examine differences in the responses of volcanic ash soils with different physicochemical properties. Soil B, rather than soil A, was a typical Andosol. During incubation at 20°C for 120 days with five dry-wet cycles, the CO₂ release rate was measured periodically. Abundance of the stable carbon isotope in CO₂ (δ¹³C-CO₂) was measured to capture changes in the origin of decomposed soil organic matter (SOM) owing to the dry-wet cycles. The CO₂ release rate under the dry-wet cycles was up to 49% higher than the values predicted from a parabolic relationship between CO₂ release and water content during incubation under the continuously constant moisture condition. The magnitude of CO₂ release enhancement was 2.7-fold higher in soil B relative to that in soil A. The δ¹³C-CO₂ value in the dry-wet cycles was enriched by 0.3–2.3‰ compared to that during incubation under the continuously constant moisture conditions, suggesting that the decomposition of well-metabolized and/or old SOM was enhanced by the dry-wet cycles. Thus, the present study suggests that Andosols, which have been believed to have a strong SOM stabilization ability, are vulnerable to dry-wet cycles. Then, increased water fluctuation in a future warmer world would have significant potential to stimulate CO₂ release from soils.     

Soil organic carbon–stock changes in Flemish grassland soils from 1990 to 2000

Total soil organic‐carbon (SOC) stocks for grassland soils in Flanders (N Belgium) were determined for the Kyoto Protocol reference year 1990 and 2000 in order to investigate whether these soils have been CO₂ sinks or sources during that period. The stocks were calculated by means of detailed SOC datasets, which were available at the community scale for the whole of Flanders. The total SOC stocks for Flemish grassland soils (1 m depth) were estimated at 38 Mt SOC in 1990 and 34 Mt SOC in 2000. The loss of SOC resulted from a decrease in the SOC content of grassland soils (71%) and could also partly (29%) be explained by a decline in grassland area. Significant decreases in %SOC for the 0–6 cm depth layer were found for the 1990s for the coarser‐textured soils with SOC losses ranging between –0.3% and –0.5% over the 10 y period. Specific management practices that disturb the SOC balance such as conversion to temporary grassland and a reduction of animal‐manure application are hypothesized to have contributed to the observed loss of SOC stocks. We furthermore conducted an analysis of uncertainty of the 1990 and 2000 grassland SOC–stocks calculation using Monte Carlo analysis. Probability‐distribution functions were determined for each of the inputs of the SOC‐stock calculation, enabling us to assess the uncertainty on the 1990 and 2000 SOC stocks. The frequency distributions of these simulated stocks both closely approached lognormal distributions, and their 95%‐confidence intervals ranged between 150% and 50% of the calculated mean SOC stock. The standard error on the measured decrease in SOC stocks in Flemish grassland soils during the 1990s was calculated to be 7–8 Tg SOC, which is equivalent to twice this decrease. This clearly shows that large‐scale changes in SOC stocks are uncertainty‐ridden, even when they are based on detailed datasets.     

Changes of soil organic carbon and its fractions in relation to soil physical properties in a long-term fertilized paddy

Soil organic carbon (SOC) has an important role in improving soil quality and sustainable production. A long-term fertilization study was conducted to investigate changes in SOC and its relation to soil physical properties in a rice paddy soil. The paddy soils analyzed were subjected to different fertilization practices: continuous application of inorganic fertilizers (NPK, N–P–K = 120–34.9–66.7 kg ha⁻¹ yr⁻¹ during 1967–1972 and 150–43.7–83.3 kg ha⁻¹ yr⁻¹ from 1973 to 2007), straw based compost (Compost, 10 Mg ha⁻¹ yr⁻¹), a combination of NPK + Compost, and no fertilization (control). Soil physical properties were investigated at rice harvesting stage in the 41st year for analyzing the relationship with SOC fraction. Continuous compost application increased the total SOC concentration in plough layers and improved soil physical properties. In contrast, inorganic or no fertilization markedly decreased SOC concentration resulting to a deterioration of soil physical health. Most of the SOC was the organo-mineral fraction (<0.053 mm size), accounting for over 70% of total SOC. Macro-aggregate SOC fraction (2–0.25 mm size), which is used as an indicator of soil quality rather than total SOC, covered 8–17% of total SOC. These two SOC fractions accumulated with the same tendency as the total SOC changes. Comparatively, micro-aggregate SOC (0.25–0.053 mm size), which has high correlation with physical properties, significantly decreased with time, irrespective of the inorganic fertilizers or compost application, but the mechanism of decrease is not clear. Conclusively, compost increased total SOC content and effective SOC fraction, thereby improving soil physical properties and sustaining production.     

Carbon sequestration in soils with annual inputs of maize biomass and maize-derived animal manure: Evidence from C abundance

The abundance of ¹³C was determined over a period of nine years in two soils (LUN, coarse sand; ASK, sandy loam) following their conversion from C3-crops and to the C4-crop silage maize (Zea mays L.). The soils were exposed to identical management and climatic conditions, and were sampled every second year. The aboveground maize biomass was either removed (stubbles and roots left), chopped and added to the soil, or fed to sheep and the faeces then added to the soil. Annual inputs of maize biomass and sheep faeces were similar (0.8 kg DM m⁻²). The study included soils maintained under C3-crops (beet roots, Beta vulgaris L.). After nine years of maize cropping, soil C from stubbles and roots accounted for 12 and 16% of the total-C in the LUN and ASK soil, respectively. Without additional organic amendment the content of total-C in the ASK soil remained constant and similar to that of soil retained under C3-crops whereas total-C tended to decrease in the LUN soil. When maize biomass and sheep faeces were added, soil total-C increased and C from these C4-sources averaged 14% and 21% of the soil total-C, respectively. Following nine annual additions, retention of C added in aboveground maize biomass averaged 19% while the retention of C added in maize-derived faeces was 30%. Our study infers that that ruminant manure C contributes about 50% more to soil C sequestration than C applied in crop residues.     

Photodegradation effects on CO2 emissions from litter and SOM and photo-facilitation of microbial decomposition in a California grassland

Decomposition of soil organic matter (SOM) and plant litter has been shown to be affected by high solar radiation; this could partly explain why biogeochemical models underestimate decomposition in arid and semi-arid ecosystems. We set out to test the effect of using traditional PVC chambers for measuring soil gas fluxes versus quartz chambers that allowed passage of light during field measurements in a dry-land field in Davis, CA. Results showed that fluxes from quartz-top chambers were on average 29% higher than from opaque chambers. We also studied the effect of solar light exposure on decomposition of native grass litter and SOM in a field experiment where plots were shaded or left exposed for 157 days during summer; litter did not seem to be affected by exposure to light. However, we concluded that SOM decomposition was affected by light exposure since shaded soil had similar respiration to sunlight-exposed soil indicating that microbial respiration occurred under the shade while photo-degradation likely occurred under the sun. Additionally, ¹⁵N-labeled grass was placed in litter bags in the field with either clear filters to allow light or aluminum covers to block light; 3-month exposure caused a change in lignin degradability as indicated by the change in the Ad/Al ratio. Incubation of that litter showed 9.3% more CO₂ produced from litter in clear and aluminum bags than unexposed litter. This showed that photo-facilitation occurred although to a small degree and was a result of light exposure and/or heat degradation. We attributed the similar respiration from clear- and aluminum-exposed litter to heat degradation of the aluminum-exposed litter. In conclusion, our results show that in hot dry ecosystems conventional PVC chambers underestimate measured CO₂ flux rates; sunlight exposure changes litter chemistry and appears to affect the degradation of soil organic matter, but the magnitude of degradation depends on an interaction of factors such as soil temperature and moisture.     

Relationship of soil phosphorus with uranium in grassland mineral soils in Ireland using soils from a long‐term phosphorus experiment and a National Soil Database

Phosphorus fertilizer contains contaminants that may increase the content in the soil and in plants. The relationship between soil P and soil uranium (U) was investigated to determine potential effects of P‐fertilizer use. This study is based on a long‐term experiment (38 years with 0, 15, and 30 kg fertilizer P ha^–1 y^–1) for beef production on grassland at Teagasc, Johnstown Castle, Wexford, Ireland and also on soils from a National Soil Database (NSD). The NSD soils were taken at fixed locations on a predetermined grid system at the density of one sample every 50 km². Of the 1310 samples in the NSD, the 760 grassland mineral soils were selected for this study. The aim was to determine to what extent P fertilizer increases the content of U in the soil. The results showed that there was a small but significant increase in soil U in the high‐P treatments, which contained high levels of soil P, in the long‐term field experiment. The results from the NSD showed that there was not a significant relationship between extractable (Morgan's) soil test P (STP) and U. It is concluded that the use of chemical P fertilizer at normal rates used in agriculture in Ireland is not a major threat to U content of soil based on the results of this study. There was a significant relationship between total P and STP, in the NSD, with the latter making up approx. 1% of the former. Soil available P increased with soil pH, probably reflecting the use of chemical P fertilizer and lime on agricultural soils.     

Soil organic matter dynamics in grassland soils under elevated CO2: Insights from long-term incubations and stable isotopes

Elevated atmospheric carbon dioxide (CO₂) levels generally stimulate carbon (C) uptake by plants, but the fate of this additional C largely remains unknown. This uncertainty is due in part to the difficulty in detecting small changes in soil carbon pools. We conducted a series of long-term (170-330 days) laboratory incubation experiments to examine changes in soil organic matter pool sizes and turnover rates in soil collected from an open-top chamber (OTC) elevated CO₂ study in Colorado shortgrass steppe. We measured concentration and isotopic composition of respired CO₂ and applied a two-pool exponential decay model to estimate pool sizes and turnover rates of active and slow C pools. The active and slow C pools of surface soils (5-10 cm depth) were increased by elevated CO₂, but turnover rates of these pools were not consistently altered. These findings indicate a potential for C accumulation in near-surface soil C pools under elevated CO₂. Stable isotopes provided evidence that elevated CO₂ did not alter the decomposition rate of new C inputs. Temporal variations in measured δ¹³C of respired CO₂ during incubation probably resulted mainly from the decomposition of changing mixtures of fresh residue and older organic matter. Lignin decomposition may have contributed to declining δ¹³C values late in the experiments. Isotopic dynamics during decomposition should be taken into account when interpreting δ¹³C measurements of soil respiration. Our study provides new understanding of soil C dynamics under elevated CO₂ through the use of stable C isotope measurements during microbial organic matter mineralization.