Biological, chemical and thermal indices of soil organic matter stability in four grassland soils

The various ecosystem functions of soil organic matter (SOM) depend on both its quantity and stability. Numerous fractionation techniques have been developed to characterize SOM stability, and thermal analysis techniques have shown promising results to describe the complete continuum of SOM in whole soil samples. However, the potential link between SOM thermal stability and biological or chemical stability has not yet been adequately explored. The objective of this study was to compare conventional chemical and biological methods used to characterize SOM stability with results obtained by thermal analysis techniques. Surface soil samples were collected from four North American grassland sites along a continental mean annual temperature gradient, each with a native and cultivated land use. Soil organic C concentrations ranged from 6.8 to 33 g C kg⁻¹ soil. Soils were incubated for 588 days at 35 °C, and C mineralization rates were determined periodically throughout the incubation by measuring CO₂ concentration using an infrared gas analyzer (IRGA) to calculate biological indices of SOM stability. Hot-water extractable organic C (HWEOC) contents were determined before and after incubation as chemical indices. Finally, samples from before and after incubation were analyzed by simultaneous thermal analysis (i.e., thermogravimetry (TG) and differential scanning calorimetry (DSC)) to determine thermal indices of SOM stability. Long-term incubation resulted in the mineralization of up to 33% of initial soil C. The number of days required to respire 5% of initial soil organic carbon (SOC), ranged from 27 to 115 days, and is proposed as a standardized biological index of SOM stability. The number of days was greater for cultivated soils compared to soils under native vegetation, and generally decreased with increasing site mean annual temperature. HWEOC (as % of initial SOC) did not show consistent responses to land use, but was significantly lower after long-term incubation. Energy density (J mg⁻¹ OM) was greater for soils under native vegetation compared to cultivated soils, and long-term incubation also decreased energy density. The temperatures at which half of the mass loss or energy release occurred typically showed larger responses to land use change than to incubation. Strong correlations demonstrated a link between the thermal and biogeochemical stability of SOM, but the interpretation of the thermal behavior of SOM in bulk soil samples remains equivocal because of the role the mineral component and organo-mineral interactions.     

The effect of warming on the vulnerability of subducted organic carbon in arctic soils

Arctic permafrost soils contain large stocks of organic carbon (OC). Extensive cryogenic processes in these soils cause subduction of a significant part of OC-rich topsoil down into mineral soil through the process of cryoturbation. Currently, one-fourth of total permafrost OC is stored in subducted organic horizons. Predicted climate change is believed to reduce the amount of OC in permafrost soils as rising temperatures will increase decomposition of OC by soil microorganisms. To estimate the sensitivity of OC decomposition to soil temperature and oxygen levels we performed a 4-month incubation experiment in which we manipulated temperature (4–20 °C) and oxygen level of topsoil organic, subducted organic and mineral soil horizons. Carbon loss (C_LOSS) was monitored and its potential biotic and abiotic drivers, including concentrations of available nutrients, microbial activity, biomass and stoichiometry, and extracellular oxidative and hydrolytic enzyme pools, were measured. We found that independently of the incubation temperature, C_LOSS from subducted organic and mineral soil horizons was one to two orders of magnitude lower than in the organic topsoil horizon, both under aerobic and anaerobic conditions. This corresponds to the microbial biomass being lower by one to two orders of magnitude. We argue that enzymatic degradation of autochthonous subducted OC does not provide sufficient amounts of carbon and nutrients to sustain greater microbial biomass. The resident microbial biomass relies on allochthonous fluxes of nutrients, enzymes and carbon from the OC-rich topsoil. This results in a “negative priming effect”, which protects autochthonous subducted OC from decomposition at present. The vulnerability of subducted organic carbon in cryoturbated arctic soils under future climate conditions will largely depend on the amount of allochthonous carbon and nutrient fluxes from the topsoil.     

Changes in mineral nitrogen, soil organic matter fractions and microbial community level physiological profiles after application of digested pig slurry and compost from municipal organic wastes to burned soils

In this study, mineralization of digested pig slurry and compost from municipal organic wastes in burned soils was followed for 60 days. The effects of amendments on organic matter fractions and microbial community level physiological profiles (CLPP) were also investigated at the end of the incubation period. Soil from a forest 10 days after a fire had a greater basal respiration, and more organic matter that a nearby soil that was not affected by fire, presumably as a consequence of black ash addition following the wildfire. Nitrification was inhibited in soils treated at 105 and 250 °C in the laboratory, but amendment application allowed nitrification to take place in the latter soil, and led to significant flushes of mineralization. Slurry amendment resulted in greater increases in mineral N compared with compost. Soil treated at 250 °C had the greatest content of water-extractable compounds (WE) at the expense of acid-extractable compounds (AE), but during the incubation the variations in these two fractions had an opposite trend, i.e. soil gained AE and lost WE fractions. The variation in N-acetyl-glucosamine-induced respiration was different between compost- and slurry-amended soils, with the greater values in the former. The effect of amendments could be further differentiated by principal component (PCA) and cluster analyses based on the variations in organic matter fractions and CLPP between the beginning and the end of the incubation period. Amendment application led to shifts on the PCA maps that depended both on the amendment and soil treatment. In fresh soil and in that treated at 250 °C, the unamended, compost- and slurry-amended treatments remained relatively close on the PCA maps and had linkage distances <1.0. In contrast, amendment application to other soils led to large shifts on the PCA maps and to linkage distances >1.0. Pig slurry led to the greatest changes in burned soil, while compost induced the greatest shifts in soil treated at 105 °C.This study suggests that an application of organic amendments after a severe fire event may contribute to a faster recovery of soil functions.     

The response of organic matter mineralisation to nutrient and substrate additions in sub-arctic soils

Global warming in the Arctic may alter decomposition rates in Arctic soils and therefore nutrient availability. In addition, changes in the length of the growing season may increase plant productivity and the rate of labile C input below ground. We carried out an experiment in which inorganic nutrients (NH₄NO₃ and NaPO₄) and organic substrates (glucose and glycine) were added to soils sampled from across the mountain birch forest-tundra heath ecotone in northern Sweden (organic and mineral soils from the forest, and organic soil only from the heath). Carbon dioxide production was then monitored continuously over the following 19 days. Neither inorganic N nor P additions substantially affected soil respiration rates when added separately. However, combined N and P additions stimulated microbial activity, with the response being greatest in the birch forest mineral soil (57% increase in CO₂ production compared with 26% in the heath soil and 8% in the birch forest organic soil). Therefore, mineralisation rates in these soils may be stimulated if the overall nutrient availability to microbes increases in response to global change, but N deposition alone is unlikely to enhance decomposition. Adding either, or both, glucose and glycine increased microbial respiration. Isotopic separation indicated that the mineralisation of native soil organic matter (SOM) was stimulated by glucose addition in the heath soil and the forest mineral soil, but not in the forest organic soil. These positive ‘priming’ effects were lost following N addition in forest mineral soil, and following both N and P additions in the heath soil. In order to meet enhanced microbial nutrient demand, increased inputs of labile C from plants could stimulate the mineralisation of SOM, with the soil C stocks in the tundra-heath potentially most vulnerable.     

Evaluating biodegradability of soil organic matter by its thermal stability and chemical composition

The stability of soil organic matter (SOM) as it relates to resistance to microbial degradation has important implications for nutrient cycling, emission of greenhouse gases, and C sequestration. Hence, there is interest in developing new ways to quantify and characterise the labile and stable forms of SOM. Our objective in this study was to evaluate SOM under widely contrasting management regimes to determine whether the variation in chemical composition and resistance to pyrolysis observed for various constituent C fractions could be related to their resistance to decomposition. Samples from the same soil under permanent pasture, an arable cropping rotation, and chemical fallow were physically fractionated (sand: 2000-50 μm; silt: 50-5 μm, and clay: <5 μm). Biodegradability of the SOM in size fractions and whole soils was assessed in a laboratory mineralization study. Thermal stability was determined by analytical pyrolysis using a Rock-Eval pyrolyser, and chemical composition was characterized by X-ray absorption near-edge structure (XANES) spectroscopy at the C and N K-edges. Relative to the pasture soil, SOM in the arable and fallow soils declined by 30% and 40%, respectively. The mineralization bioassay showed that SOM in whole soil and soil fractions under fallow was less susceptible to biodegradation than that in other management practices. The SOM in the sand fraction was significantly more biodegradable than that in the silt or clay fractions. Analysis by XANES showed a proportional increase in carboxylates and a reduction in amides (protein) and aromatics in the fallow whole soil compared to the pasture and arable soils. Moreover, protein depletion was greatest in the sand fraction of the fallow soil. Sand fractions in fallow and arable soils were, however, relatively enriched in plant-derived phenols, aromatics, and carboxylates compared to the sand fraction of pasture soils. Analytical pyrolysis showed distinct differences in the thermal stability of SOM among the whole soil and their size fractions; it also showed that the loss of SOM generally involved preferential degradation of H-rich compounds. The temperature at which half of the C was pyrolyzed was strongly correlated with mineralizable C, providing good evidence for a link between the biological and thermal stability of SOM.     

Quality and potential biodegradability of soil organic matter preserved in permafrost of Siberian tussock tundra

Soil organic matter (SOM) quality and biodegradability the permafrost underlying Siberian wet tussock tundra (Kolyma river basin, northeast Siberia) were analyzed and compared to the characteristics of the contemporary active layer. For this purpose, three permafrost affected soil cores (down to 3 m depth) and seven active layer soil cores (down to 0.3 m depth) were sampled. The samples were divided into particular layers, which were analyzed separately. SOM stability was assessed using a simple chemical fractionation (sequential extraction by cold and hot water, and hot acid). SOM biodegradability and soil mineralization potentials were tested in short-term laboratory incubations. The active layer contained 24 kg C m⁻² and 70 kg C m⁻² was preserved in 3 m of permafrost. The chemical quality and biodegradability of permafrost SOM were very similar to that of the active layer mineral horizon, and independent from depth. The only exceptions were (1) higher solubility of permafrost SOM in water, indicating its higher mobility and potential leakage after permafrost thawing and (2) higher nutrient (N, P) concentrations available to a dense permafrost microbial community, which could support decomposition of more complex substrates under suitable temperature conditions after thawing. The mineralization potential of the upper 1 m deep permafrost, which could melt by 2100 according to permafrost degradation models, was 6.7 g C m⁻² d⁻¹ (optimum conditions of 20 °C, field water capacity), which is comparable to that of the contemporary active layer of 0.5 m depth (7.5 g C m⁻² d⁻¹). Under field conditions, SOM mineralization rate would reasonably be significantly lower due to prevailing anoxia (high water table) and diffusion constraints in the deep and flooded soil profile.We conclude from our results that the permafrost (1) cryopreserves a high SOM amount, which is distributed to considerable depths, being of similar chemical quality and biodegradability to that of the active layer mineral horizon SOM, and (2) contains a dense living microbial community, which is able to decompose the present SOM rapidly without any obvious chemical limitation under suitable conditions.     

Soil organic C stabilization and thresholds in C saturation

When building soil organic matter (SOM) contents in agricultural production systems, stabilization of both pre-existing as well as added C is important. A laboratory mineralization experiment was conducted over 374 days to evaluate the effect of pre-existing SOM on soil C mineralization after addition of organic matter (OM) using sugar cane. The SOM gradient used here stretched from 21 to 106 g C kg⁻¹ soil and was a result of different periods of continuous cultivation of 5, 20, 35 and 105 years in comparison to a forest soil. The rate of organic C mineralization was found to be dependent on the status of pre-existing soil organic C (SOC). Highly degraded soil which had been under continuous cultivation for 35 years and more showed the highest rate of C mineralization per unit SOC (117.9 mg C g⁻¹ C) while forest soil had the lowest amount of C mineralized per unit SOC (73.5 mg C g⁻¹ C). Forest soil had the highest amount of increased C mineralization as a result of organic matter (OM) additions (8.0 mg C g⁻¹ soil) followed by the highly degraded soil that had been under cultivation for 105 years (5.5 mg C g⁻¹ soil). Additional mineralized C as a function of time after forest conversion declined progressively within the first 20 years of continuous soil use. Soil which had been under continuous cultivation for 20 years had the lowest amount of additional mineralized C (4.0 mg C g⁻¹ soil). SOM stabilization efficiency in the studied soils appears to be highest with intermediate cultivation history of about 20 years. These soils that have been recently converted to cultivation also appear to have a greater ability to stabilize added OM than the most degraded soils investigated in this study. It is thus advisable to provide intervention strategies to reverse SOM decline for farming communities at an intermediate stage before the soils are highly depleted of SOC.     

Phenol oxidase, peroxidase and organic matter dynamics of soil

Extracellular enzymes mediate the degradation, transformation and mineralization of soil organic matter. The activity of cellulases, phosphatases and other hydrolases has received extensive study and in many cases stoichiometric relationships and responses to disturbances are well established. In contrast, phenol oxidase and peroxidase activities, which are often uncorrelated with hydrolase activities, have been measured in only a small subset of soil enzyme studies. These enzymes are expressed for a variety of purposes including ontogeny, defense and the acquisition of carbon and nitrogen. Through excretion or lysis, these enzymes enter the environment where their aggegrate activity mediates key ecosystem functions of lignin degradation, humification, carbon mineralization and dissolved organic carbon export. Phenol oxidases and peroxidases are less stable in the environment than extracellular hydrolases, especially when associated with organic particles. Activities are also affected, positively and negatively, by interaction with mineral surfaces. High spatiotemporal variation obscures their relationships with environmental variables and ecological process. Across ecosystems, phenol oxidase and peroxidase activities generally increase with soil pH, a finding not predicted from the pH optima of purified enzymes. Activities associated with plant litter and particulate organic matter often correlate with decomposition rates and potential activities generally increase with the lignin and secondary compound content of the material. At the ecosystem scale, nitrogen amendment alters the expression of phenol oxidase and peroxidase enzymes more broadly than culture studies imply and these responses correlate with positive and negative changes in litter decomposition rates and soil organic matter content. At the global scale, N amendment of basidiomycete-dominated soils of temperate and boreal forest ecoystems often leads to losses of oxidative enzyme activity, while activities in grassland soils dominated by glomeromycota and ascomycetes show little net response. Land use that leads to loss of soil organic matter tends to increase oxidative activities. Across ecosystems, soil organic matter content is not correlated with mean potential phenol oxidase and peroxidase activities. A multiple regression model that includes soil pH, mean annual temperature, mean annual precipitation and potential phenol oxidase activity accounts for 37% of the variation in soil organic matter (SOM) content across ecosystems (n = 63); a similar model for peroxidase activity describes 32% of SOM variance (n = 43). Analysis of residual variation suggest that suites of interacting factors create both positive and negative feedbacks on soil organic matter storage. Soils with high oxygen availability, pH and mineral activity tend to be substrate limited: high in situ oxidative activities limit soil organic matter accumulation. Soils with opposing characteristics are activity limited: low in situ oxidative activities promote soil organic matter storage.     

Rhizosphere priming can promote mobilisation of N-rich compounds from soil organic matter

Soil organic matter (SOM) is the dominant store of nutrients required for plant growth, but the availability of these nutrients is dependent on transformations mediated by the microbial biomass. The addition of labile C to soil is known to alter SOM turnover (priming effect, PE), but understanding of this is limited, particularly with respect to impact on gross nitrogen (N) fluxes. Here we examined relationships between C and N fluxes from SOM under primed and non-primed conditions in two soils. Stable isotopes (¹³C and ¹⁵N) were used to measure gross C and N fluxes from SOM and to differentiate between SOM mineralised due to priming and that from basal mineralisation. ¹³C-glucose was added daily to simulate the effect of addition of labile C on SOM-C and –N mineralisation within the rhizosphere. Addition of glucose increased both gross N and C mineralisation from SOM. However, the C-to-N ratio of the mineralised flux from ‘primed’ SOM was 5:1, whereas the C-to-N ratio of the basal mineralised flux was 20:1 indicating that priming acted on specific organic matter pools. This result is consistent with the concept that priming is a distinct N-mining response of the microbial biomass, as opposed to an acceleration of the basal flux. Our data suggest that C and N fluxes are not directly linked through their gross stoichiometry in SOM. This is due to the heterogeneity and overall passiveness of OM relative to the dynamic nature of mineralisation fluxes and source pools, and in primed systems the mineralisation of N-rich compounds.     

Mineralisation and humification of plant matter in soil samples as a tool in the testing of soil quality

Since life is inevitably dependent on the assimilation and dissimilation of carbon, and since most of the organic carbon is bound in soil humic matter, the mineralisation and humification of plant carbon in soil should be monitored, so as to evaluate soil quality and avoid ecological risks. For this reason we suggested an incubation test of thirty days in duration with soil samples amended or not with lucerne meal as a source of plant carbon. During the incubation period, CO₂ release is to be measured repeatedly, and thereafter contents of humic acids (HA) and fulvic acids (FA) should be estimated and compared with those determined in the original soil samples. Our results obtained with samples from non-fertilized or long-term (?>?40 years) fertilized plots of two field trials indicate that fertilization by NPK?+ farm yard manure resulted in (i) a slight enhancement of C mineralisation, i.e., CO₂ release from soil, and (ii) a significant increases of HA and FA contents. Soil samples from a reclaimed mine spoil, and either fertilised or not with sewage sludge did not show distinct differences in the same parameters. The practicability of the incubation test as a tool in the monitoring of soil quality should be further proved using samples from differently affected soils.     

Comments on the regulatory gate hypothesis and implications for C-cycling in soil

The paper by Kemmitt et al. [2008. Mineralization of native soil organic matter is not regulated by the size, activity or composition of the soil microbial biomass - a new perspective. Soil Biology and Biochemistry 40, 61-73] proposing the existence of an abiotic regulatory gate that controls the rate-limiting step of stabilised soil organic matter (SOM) mineralization, has initiated a fundamental and far-reaching debate. In this contribution the implications of a functioning abiotic regulatory gate are considered in the context of microbial community diversity and soil carbon cycling. I argue that although the evidence presented in support of the regulatory gate is strong, abiotic routes for SOM-mineralization function in parallel with biologically mediated mechanisms. Evidence is now accumulating that, in the presence of plant-inputs to soil, enhanced microbial mobilisation of SOM into biomass is a quantitatively important and ubiquitous process. I argue that this mineralization of SOM is fuelled by energy-rich substrates and is driven by microbial nutrient-demand. This implies that the mineralization of stabilised SOM and the turnover of C-inputs from current vegetation are intimately linked through the functioning of microbial communities associated with plants. This suggests that the microbial ‘eye of the needle’ is a crucial control-point in determining the carbon balance of soils. Fortunately, there are now excellent methods that allow quantification of SOM- and plant-derived C-fluxes through the members of soil microbial communities, and will also allow quantification of the relative importance of the abiotic and biotic routes of SOM-mineralization.     

Influence of soil compaction on carbon and nitrogen mineralization of soil organic matter and crop residues

 We studied the influence of soil compaction in a loamy sand soil on C and N mineralization and nitrification of soil organic matter and added crop residues. Samples of unamended soil, and soil amended with leek residues, at six bulk densities ranging from 1.2 to 1.6 Mg m^–3 and 75% field capacity, were incubated. In the unamended soil, bulk density within the range studied did not influence any measure of microbial activity significantly. A small (but insignificant) decrease in nitrification rate at the highest bulk density was the only evidence for possible effects of compaction on microbial activity. In the amended soil the amounts of mineralized N at the end of the incubation were equal at all bulk densities, but first-order N mineralization rates tended to increase with increasing compaction, although the increase was not significant. Nitrification in the amended soils was more affected by compaction, and NO₃ ^–-N contents after 3 weeks of incubation at bulk densities of 1.5 and 1.6 Mg m^–3 were significantly lower (by about 8% and 16% of total added N, respectively), than those of the less compacted treatments. The C mineralization rate was strongly depressed at a bulk density of 1.6 Mg m^–3, compared with the other treatments. The depression of C mineralization in compacted soils can lead to higher organic matter accumulation. Since N mineralization was not affected by compaction (within the range used here) the accumulated organic matter would have had higher C : N ratios than in the uncompacted soils, and hence would have been of a lower quality. In general, increasing soil compaction in this soil, starting at a bulk density of 1.5 Mg m^–3, will affect some microbially driven processes. Received: 10 June 1999     

Temperature sensitivity of organic matter decomposition in two boreal forest soil profiles

Controversial conclusions from different studies suggest that the decomposition of old soil organic matter (SOM) is either more, less, or equally temperature sensitive compared to the younger SOM. Based on chemical kinetic theory, the decomposition of more recalcitrant materials should be more temperature sensitive, unless environmental factors limit decomposition. Here, we show results for boreal upland forest soils supporting this hypothesis. We detected differences in the temperature sensitivity 1) between soil layers varying in their decomposition stage and SOM quality, and 2) inside the layers during a 495 day laboratory incubation. Temperature sensitivity increased with increasing soil depth and decreasing SOM quality. In the organic layers, temperature sensitivity of decomposition increased during the early part of a 495 day laboratory incubation, after respiration rate and SOM quality had notably decreased. This indicates that decomposition of recalcitrant compounds was more temperature sensitive than that of the labile ones. Our results imply that Q₁₀ values for total heterotrophic soil respiration determined from short-term laboratory incubations can either underestimate or overestimate the temperature sensitivity of SOM decomposition, depending on soil layer, initial labile carbon content and temperature range used for the measurements. Using Q₁₀ values that ignore these factors in global climate models provides erroneous estimates on the effects of climate change on soil carbon storage.     

Mineralization and carbon turnover in subarctic heath soil as affected by warming and additional litter

Arctic soil carbon (C) stocks are threatened by the rapidly advancing global warming. In addition to temperature, increasing amounts of leaf litter fall following from the expansion of deciduous shrubs and trees in northern ecosystems may alter biogeochemical cycling of C and nutrients. Our aim was to assess how factorial warming and litter addition in a long-term field experiment on a subarctic heath affect resource limitation of soil microbial communities (measured by thymidine and leucine incorporation techniques), net growing-season mineralization of nitrogen (N) and phosphorus (P), and carbon turnover (measured as changes in the pools during a growing-season-long field incubation of soil cores in situ). The mainly N limited bacterial communities had shifted slightly towards limitation by C and P in response to seven growing seasons of warming. This and the significantly increased bacterial growth rate under warming may partly explain the observed higher C loss from the warmed soil. This is furthermore consistent with the less dramatic increase in the contents of dissolved organic carbon (DOC) and dissolved organic N (DON) in the warmed soil than in the soil from ambient temperature during the field incubation. The added litter did not affect the carbon content, but it was a source of nutrients to the soil, and it also tended to increase bacterial growth rate and net mineralization of P. The inorganic N pool decreased during the field incubation of soil cores, especially in the separate warming and litter addition treatments, while gross mineralized N was immobilized in the biomass of microbes and plants transplanted into the incubates soil cores, but without any significant effect of the treatments. The effects of warming plus litter addition on bacterial growth rates and of warming on C and N transformations during field incubation suggest that microbial activity is an important control on the carbon balance of arctic soils under climate change.     

The priming potential of biochar products in relation to labile carbon contents and soil organic matter status

Recognition of biochar as a potential tool for long-term carbon sequestration with additional agronomic benefits is growing. However, the functionality of biochar in soil and the response of soils to biochar inputs are poorly understood. It has been suggested, for example, that biochar additions to soils could prime for the loss of native organic carbon, undermining its sequestration potential. This work examines the priming potential of biochar in the context of its own labile fraction and procedures for their assessment. A systematic set of biochar samples produced from C4 plant biomass under a range of pyrolysis process conditions were incubated in a C3 soil at three discrete levels of organic matter status (a result of contrasting long-term land management on a single site). The biochar samples were characterised for labile carbon content ex-situ and then added to each soil. Priming potential was determined by a comparison of CO₂ flux rates and its isotopic analysis for attribution of source. The results conclusively showed that while carbon mineralisation was often higher in biochar amended soil, this was due to rapid utilisation of a small labile component of biochar and that biochar did not prime for the loss of native organic soil organic matter. Furthermore, in some cases negative priming occurred, with lower carbon mineralisation in biochar amended soil, probably as a result of the stabilisation of labile soil carbon.     

Microbial processes controlling P availability in forest spodosols as affected by soil depth and soil properties

Because carbon dioxide (CO₂) concentration is rising, increases in plant biomass and productivity of terrestrial ecosystems are expected. However, phosphorus (P) unavailability may disable any potential enhanced growth of plants in forest ecosystems. In response to P scarcity under elevated CO₂, trees may mine deeper the soil to take up more nutrients. In this scope, the ability of deep horizons of forest soils to supply available P to the trees has to be evaluated. The main objective of the present study was to quantify the relative contribution of topsoil horizons and deep horizons to P availability through processes governed by the activity of soil micro-organisms. Since soil properties vary with soil depth, one can therefore assume that the role of microbial processes governing P availability differs between soil layers. More specifically, our initial hypothesis was that deeper soil horizons could substantially contribute to total plant available P in forested ecosystems and that such contribution of deep horizons differs among sites (due to contrasting soil properties). To test this hypothesis, we quantified microbial P and mineralization of P in ‘dead’ soil organic matter to a depth of 120 cm in forest soils contrasting in soil organic matter, soil moisture and aluminum (Al) and iron (Fe) oxides. We also quantified microbiological activity and acid phosphomonoesterase activity. Results showed that the role of microbial processes generally decreases with increasing soil depth. However, the relative contribution of surface (litter and 0–30 cm) and deep (30–120 cm) soil layers to the stocks of available P through microbial processes (51–62 kg P ha^?1) are affected by several soil properties, and the contribution of deep soil layers to these stocks vary between sites (from 29 to 59%). This shows that subsoils should be taken into account when studying the microbial processes governing P availability in forest ecosystems. For the studied soils, microbial P and mineralization of P in ‘dead’ soil organic matter particularly depended on soil organic matter content, soil moisture and, to a minor extent, Al oxides. High Al oxide contents in some sites or in deep soil layers probably result in the stabilization of soil organic compounds thus reducing microbiological activity and mineralization rates. The mineralization process in the litter also appeared to be P-limited and depended on the C:P ratio of soil organic matter. Thus, this study highlighted the effects of soil depth and soil properties on the microbial processes governing P availability in the forest spodosols.     

Pasture degradation impacts soil phosphorus storage via changes to aggregate-associated soil organic matter in highly weathered tropical soils

Maintaining the productivity of tropical pastures is a major challenge for the sustainable management of tropical landscapes around the globe. To address this issue, we examined linkages between soil organic matter (SOM), aggregation, and phosphorus (P) dynamics by comparing productive vs. degraded pastures in the deforested Amazon Basin of Colombia. Paired plots of productive (dominated by planted Brachiaria spp.) vs. degraded pasture were identified on nine farms in the Department of Caquetá and sampled during the rainy season of 2011. Aboveground pasture biomass production and nutrient content were measured. Surface soils (0–10 cm) were also fractionated by wet sieving, and C, ¹³C, N and P contents were analyzed for the bulk soil and various aggregate size classes. Productive pastures yielded more than double the aboveground biomass compared to degraded pastures (during a 35 day regrowth period following cutting), with over 60% higher N and P contents in this material. Similar trends were observed for the standing litter biomass and nutrient contents. Soil aggregate stability was found to differ between pasture types, with a mean weight diameter of 3590 vs. 3230 μm in productive vs. degraded pastures, respectively. Productive pastures were found to have 20% higher total soil C and N contents than degraded pastures. While there was no difference in total P content between pasture types, organic P was found to be nearly 40% higher in soils of productive vs. degraded pastures. Differences in total SOM between pasture types were largely explained by a higher C content in the large macroaggregate fraction (>2000 μm), and more specifically in the microaggregates (53–250 μm) occluded within this fraction. These findings confirm the role of microaggregates within macroaggregates as a preferential site for the physical stabilization of SOM, and furthermore, suggest that it may serve as a useful diagnostic fraction for evaluating management impacts on SOM in tropical pasture systems. Similar to trends observed for C and N, total P content was 25% higher in the microaggregates within large macroaggregates of productive vs. degraded pasture soils. This correspondence between C and total P contents in large macroaggregate fractions, along with elevated levels of organic P in productive pastures, suggests that this P is likely in an organic form and that there is a close link between soil structure, SOM dynamics and the maintenance of organic P in these soils. Given the potential relevance of organic P for efficient P cycling in these soils, our findings offer critical new insight for the management of SOM and aggregate-associated P pools in tropical pasture systems.     

Scots pine (Pinus sylvestris L.) roots and soil moisture did not affect soil thermal sensitivity

Through their effects on microbial metabolism, temperature and moisture affect the rate of decomposition of soil organic matter. Plant roots play an important role in SOM mineralization and nutrient cycling. There are reports that rhizosphere soil exhibits higher sensitivity to temperature than root-free soil, and this can have implications for how soil CO₂ efflux may be affected in a warmer world. We tested the effects of 1-week incubation under different combinations of temperature (5, 15, 30 ^°C) and moisture (15, 50, 100% WHC) on the respiration rate of soil planted with Scots pine and of unplanted soil. Soil respiration in both soils was the highest at moderate moisture (p < 0.0001) and, increased with temperature (p < 0.0001). There was also marginally significant effect of soil kind on respiration rate (p < 0.055), but the significant interaction of temperature effect with soil kind effect, indicated, that soil respiration of planted soil was higher than unplanted soil only at 5 ^°C (p < 0.05). The soil kind effect was compared also as Q₁₀ coefficients for respiration rate, showing the relative change in microbial activity with increased temperature. However, there was no difference in the thermal sensitivity of soil respiration between planted and unplanted soils (p = 0.99), irrespective of the level of soil moisture. These findings were similar to the latest studies and confirmed, that in various models, being useful tools in studying of soil carbon cycling, there is no need to distinguish between planted and unplanted soil as different soil carbon pools.     

Determination and use of a corrected control factor in the chloroform fumigation method of estimating soil microbial biomass

Estimates of soil microbial biomass are important for both comparative system analysis and mechanistic models. The method for measuring microbial biomass that dominates the literature is the chloroform fumigation incubation method (CFIM), developed on the premise that killed microorganisms are readily mineralized to CO₂, which is a measure of the initial population. Factors that effect the CFIM have been thoroughly investigated over the last 15 years. A question that still remains after countless experiments is the use of an appropriate nonfumigated control for accounting for native soil organic matter (SOM) mineralization during incubation. Our approach was to add hot-water-leached ¹⁴C-labeled straw to both fumigated and nonfumigated samples assuming the straw would mimic a recalcitrant C substrate fraction of SOM. The ratio of the ¹⁴C evolved from the fumigated sample over the ¹⁴C evolved from the control sample would provide a corrected control value to be used in calculating microbial biomass. This experiment was conducted on soils from forest, agricultural, grassland and shrub-steppe ecosystems. The results clearly indicate that equal recalcitrant C mineralization during incubation is not a valid assumption. The results with these soils indicate than on the average only 20% of the control CO₂ should be subtracted from the fumigated CO₂ for the biomass calculation. The correction value ranged from 18% for agricultural soils to 25% for shrub-steppe soil, with the average correction value being 20%. Our experiments show that corrected biomass values will be 1.5–2 times greater than uncorrected biomass values. In addition using a corrected control improved the 1:1 correlation between the CFIM and SIR methods for these soils.     

Kinetics of native and added carbon mineralization on incubating at different soil and moisture conditions in Typic Ustochrepts and Typic Halustalf

The carbon dynamics in soils is of great importance due to its links to the global carbon cycle. The prediction of the behavior of native soil organic carbon (SOC) and organic amendments via incubation studies and mathematical modeling may bridge the knowledge gap in understanding complex soil ecosystems. Three alkaline Typic Ustochrepts and one Typic Halustalf with sandy, loamy sand, and clay loam texture, varying in percent SOC of 0.2; S₁, 0.42; S₂, 0.67; S₃ and 0.82; S₄ soils, were amended with wheat straw (WS), WS + P, sesbania green manure (GM), and poultry manure (PM) on 0.5% C rate at field capacity (FC) and ponding (P) moisture levels and incubated at 35 °C for 1, 15, 30 and 45 d. Carbon mineralization was determined via the alkali titration method after 1, 5, 7 14, 21, and 28 d. The SOC and inorganic carbon contents were determined from dried up (50 °C) soil samples after 1, 15, 30, and 45 d of incubation. Carbon from residue mineralization was determined by subtracting the amount of CO₂-C evolved from control soils. The kinetic models; monocomponent first order, two-component first order, and modified Gompertz equations were fitted to the carbon mineralization data from native and added carbon. The SOC decomposition was dependent upon soil properties, and moisture, however, added C was relatively independent. The carbon from PM was immobilized in S₄. All the models fitted to the data predicted carbon mineralization in a similar range with few exceptions. The residues lead to the OC build-up in fine-textured soils having relatively high OC and cation exchange capacities. Whereas, fast degradation of applied OC in coarse-textured soils leads to faster mineralization and lower build-up from residues. The decline in CaCO₃ after incubation was higher at FC than in the P moisture regime.