Observed and modelled soil carbon and nitrogen changes after planting a Pinus radiata stand onto former pasture

After reforesting pasture land, it is often observed that soil carbon stocks decrease. The present work reports findings from a site near Canberra, Australia, where a pine forest (Pinus radiata) was planted onto a former unimproved pasture site. We report a number of detailed observations seeking to understand the basis of the decline in soil C stocks. This is supported by simulations using the whole-ecosystem carbon and nitrogen cycling model CenW 3.1. The model indicated that over the first 18 years after forest establishment, the site lost about 5.5 t C ha^?1 and 588 kgN ha^?1 from the soil. The C:N ratio of soil organic matter did not change in a systematic manner over the observational period. Carbon and nitrogen stocks contained in the biomass of the 18-year old pine stand exceeded that of the pasture by 88 t C ha^?1 and 393 kgN ha^?1. An additional 6.1 t C ha^?1 and 110 kgN ha^?1 accumulated in above-ground litter. These changes, together with the vertical distribution of carbon and nitrogen in the soil, agreed well with the observation at the site. It was assumed that over 18 years, there was also a loss of 86 kgN ha^?1 from the ecosystem because of normal gaseous losses during nitrogen turn-over and a small amount of nitrogen leaching. Those losses could not be replenished in the pine system without symbiotic biological nitrogen fixation, and there were no fertiliser additions. A simple mass balance approach indicated that the amount of nitrogen accumulating in plant biomass and the litter layer plus the assumed nitrogen loss from the site matched the amount of nitrogen lost from the soil organic nitrogen pool. This reduction in soil nitrogen, together with an unchanged C:N ratio, provided a simple and internally consistent explanation for the observed reduction of soil carbon after reforestation. It supports the general notion that trends in soil carbon upon land-use change can often be controlled by the possible fates of available soil nitrogen.     

Dynamics of litter carbon turnover and microbial abundance in a rye detritusphere

Factors determining C turnover and microbial succession at the small scale are crucial for understanding C cycling in soils. We performed a microcosm experiment to study how soil moisture affects temporal patterns of C turnover in the detritusphere. Four treatments were applied to small soil cores with two different water contents (matric potential of ?0.0063 and ?0.0316 MPa) and with or without addition of ¹³C labelled rye residues (δ¹³C=299‰), which were placed on top. Microcosms were sampled after 3, 7, 14, 28, 56 and 84 days and soil cores were separated into layers with increasing distance to the litter. Gradients in soil organic carbon, dissolved organic carbon, extracellular enzyme activity and microbial biomass were detected over a distance of 3 mm from the litter layer. At the end of the incubation, 35.6% of litter C remained on the surface of soils at ?0.0063 MPa, whereas 41.7% remained on soils at ?0.0316 MPa. Most of the lost litter C was mineralised to CO₂, with 47.9% and 43.4% at ?0.0063 and ?0.0316 MPa, respectively. In both treatments about 6% were detected as newly formed soil organic carbon. During the initial phase of litter decomposition, bacteria dominated the mineralisation of easily available litter substrates. After 14 days fungi depolymerised more complex litter compounds, thereby producing new soluble substrates, which diffused into the soil. This pattern of differential substrate usage was paralleled by a lag phase of 3 days and a subsequent increase in enzyme activities. Increased soil water content accelerated the transport of soluble substrates, which influenced the temporal patterns of microbial growth and activity. Our results underline the importance of considering the interaction of soil microorganisms and physical processes at the small scale for the understanding of C cycling in soils.     

Effects of tillage,organic resources and nitrogen fertiliser on soil carbon dynamics and crop nitrogen uptake in semi-arid West Africa

Tillage, organic resources and fertiliser effects on soil carbon (C) dynamics were investigated in 2000 and 2001 in Burkina Faso (West Africa). A split plot design with four replications was laid-out on a loamy-sand Ferric Lixisol with till and no-till as main treatments and fertiliser types as sub-treatments. Soil was fractionated physically into coarse (0.250–2 mm), medium (0.053–0.250 mm) and fine fractions (< 0.053 mm). Particulate organic carbon (POC) accounted for 47–53% of total soil organic carbon (SOC) concentration and particulate organic nitrogen (PON) for 30–37% of total soil nitrogen concentration. The POC decreased from 53% of total SOC in 2000 to 47% of total SOC in 2001. Tillage increased the contribution of POC to SOC. No-till led to the lowest loss in SOC in the fine fraction compared to tilled plots. Well-decomposed compost and single urea application in tilled as well as in no-till plots induced loss in POC. Crop N uptake was enhanced in tilled plots and may be up to 226 kg N ha⁻¹ against a maximum of 146 kg N ha⁻¹ in no-till plots. Combining crop residues and urea enhanced incorporation of new organic matter in the coarse fraction and the reduction of soil carbon mineralisation from the fine fraction. The PON and crop N uptake are strongly correlated in both till and no-till plots. Mineral-associated N is more correlated to N uptake by crop in tilled than in no-till plots. Combining recalcitrant organic resources and nitrogen fertiliser is the best option for sustaining crop production and reducing soil carbon decline in the more stabilised soil fraction in the semi-arid West Africa.     

Mechanisms of short-term soil carbon storage in experimental grasslands

We investigated the fate of root and litter derived carbon in soil organic matter and dissolved organic matter in soil profiles, in order to explain mechanisms of short-term soil carbon storage. A time series of soil and soil solution samples was investigated at the field site of The Jena Experiment between 2002 and 2004. In addition to the main experiment with C3 plants, a C4 species (Amaranthus retroflexus L.) naturally labeled with ¹³C was grown on an extra plot. Changes in organic carbon concentration in soil and soil solution were combined with stable isotope measurements to follow the fate of plant carbon into the soil and soil solution. A split plot design with plant litter removal versus double litter input simulated differences in biomass input. After 2 years, the no litter and double litter treatment, respectively, showed an increase of 381 g C m^?2 and 263 g C m^?2 to 20 cm depth, while 71 g C m^?2 and 393 g C m^?2 were lost between 20 and 30 cm depth. The isotopic label in the top 5 cm indicated that 115 g C m^?2 and 156 g C m^?2 of soil organic carbon were derived from C4 plant material on the no litter and the double litter treatment, respectively. Without litter, this equals the total amount of 97 g C m^?2 that was newly stored in the same soil depth, whereas with double litter this clearly exceeded the stored amount of 75 g C m^?2. Our results indicate that litter input resulted in lower carbon storage and larger carbon losses and consequently accelerated turnover of soil organic carbon. Isotopic evidence showed that inherited soil organic carbon was replaced by fresh plant carbon near the soil surface. Our results suggest that primarily carbon released from soil organic matter, not newly introduced plant organic matter, was transported in the soil solution. However, the total flow of dissolved organic carbon was not sufficient to explain the observed carbon storage in deeper soil layers, and the existence of additional carbon uptake mechanisms is discussed.     

Indicators of soil ecosystem services in conventional and organic arable fields along a gradient of landscape heterogeneity in southern Sweden

Agricultural intensification has been vital for meeting global food demand but has caused environmental degradation. This has disrupted the ability of soil to provide vital ecosystem services. Organic farming is often thought to conserve and utilise soil ecosystem services, and thus be a more sustainable method of food production than conventional farming. However, evidence for this is equivocal, and little is known of the potential trade-offs between soil functions, which can be classified as supporting and provisioning ecosystem services, in conventional and organic systems. In addition, few studies have simultaneously examined how surrounding landscape heterogeneity affects soil functions in agriculture. In this study we investigated the effects of farming method (conventional versus organic) and landscape heterogeneity (100 m, 500 m and 1000 m radius) on indicators of soil ecosystem services: soil organic carbon (SOC), total nitrogen (TN), water holding capacity (WHC) and plant-available phosphorous (P) (measures of carbon storage and nutrient retention); net N mineralisation and microbial community composition and biomass (nutrient cycling); and crop yield. We found no effect of landscape heterogeneity, and no differences in any of the measured soil and microbial variables between conventional and organic farms, apart from net N mineralisation, which was higher in organic farms. However, conventional farms had significantly greater yield than organic farms, and there was no apparent trade-off between increasing yield and the level of supporting ecosystem services. The organic farms in this study appear to have been intensively managed, with a straight substitution of organic inputs for chemicals, but little other effort to enhance soil fertility. For example, the organic farms applied large quantities of manure compared with conventional farms but conducted mechanical weeding (harrowing), whereas conventional farms applied herbicides. This repeated soil disturbance may cause rapid organic matter mineralisation and undermine the ability of these organic farms to retain carbon and nitrogen. The terms ‘organic’ and ‘conventional’ agriculture both cover a wide variety of farming methods, some of which enhance or deplete ecosystem services more than others. To develop truly sustainable methods of agriculture, research should focus on the effects of specific farming practices, rather than the labels ‘conventional’ and ‘organic’.     

Differences in soil enzyme activities,microbial community structure and short-term nitrogen mineralisation resulting from farm management history and organic matter amendments

Changes in soil microbial biomass, enzyme activities, microbial community structure and nitrogen (N) dynamics resulting from organic matter amendments were determined in soils with different management histories to gain better understanding of the effects of long- and short-term management practices on soil microbial properties and key soil processes. Two soils that had been under either long-term organic or conventional management and that varied in microbial biomass and enzyme activity levels but had similar fertility levels were amended with organic material (dried lupin residue, Lupinus angustifolius L.) at amounts equivalent to 0, 4 and 8 t dry matter lupin ha^?1. Microbial biomass C and N, arginine deaminase activity, fluorescein diacetate hydrolysis, dehydrogenase enzyme activity and gross N mineralisation were measured in intervals over an 81-day period. The community structure of eubacteria and actinomycetes was examined using PCR–DGGE of 16S rDNA fragments. Results suggested that no direct relationships existed between microbial community structure, enzyme activities and N mineralisation. Microbial biomass and activity changed as a result of lupin amendment whereas the microbial community structure was more strongly influenced by farm management history. The addition of 4 t ha^?1 of lupin was sufficient to stimulate the microbial community in both soils, resulting in microbial biomass growth and increased enzyme activities and N mineralisation regardless of past management. Amendment with 8 t lupin ha^?1 did not result in an increase proportional to the extra amount added; levels of soil microbial properties were only 1.1–1.7 times higher than in the 4 t ha^?1 treatment. Microbial community structure differed significantly between the two soils, while no changes were detected in response to lupin amendment at either level during the short-term incubation. Correlation analyses for each treatment separately, however, revealed differences that were inconsistent with results obtained for soil biological properties suggesting that differences might exist in the structure or physiological properties of a microbial component that was not assessed in this study.     

Estimating heterotrophic and autotrophic soil respiration in a semi-natural forest of Lombardy,Italy

We studied a semi-natural forest in Northern Italy that was set aside more than 50 years ago, in order to better understand the soil carbon cycle and in particular the partitioning of soil respiration between autotrophic and heterotrophic respiration. Here we report on soil organic carbon, root density, and estimates of annual fluxes of soil CO₂ as measured with a mobile chamber system at 16 permanent collars about monthly during the course of a year. We partitioned between autotrophic and heterotrophic respiration by the indirect regression method, which enabled us to obtain the seasonal pattern of single components.The soil pool of organic carbon, with 15.8 (±4.5) kg m^?2, was very high over the entire depth of 45 cm. The annual respiration rates ranged from 0.6 to 6.9 μmol CO₂ m^?2 s^?1 with an average value of 3.4 (±2.3) μmol CO₂ m^?2 s^?1, and a cumulative flux of 1.1 kg C m^?2 yr^?1. The heterotrophic component accounted for 66% of annual CO₂ efflux. Soil temperature largely controlled the heterotrophic respiration (R² = 0.93), while the autotrophic component followed irradiation, pointing to the role of photosynthesis in modulating the annual course of soil respiration.Most studies on soil respiration partitioning indicate autotrophic root respiration as a first control of the spatial variability of the overall respiration, which originates mainly from the uppermost soil layers. Instead, in our forest the spatial variability of soil respiration was mainly linked to soil carbon, and deeper layers seemed to provide a significant contribution to soil respiration, a feature that may be typical for an undisturbed, naturally maturing ecosystem with well developed pedobiological processes and high carbon stocks.     

Carbon replacement and stability changes in short-term silvo-pastoral experiments in Colombian Amazonia

There is little information on the effects of land use change on soil Carbon stocks in Colombian Amazonia. Such information would be needed to assess the impact of this area on the global C cycle and the sustainability of agricultural systems that are replacing native forest. The aim of this study was to evaluate soil carbon stocks and changes after the clearing of the native forest, the establishment of pastures and the reclamation of the degraded pasture, in Caquetá, Colombia.We compared the contents of Total C, Oxidizable C and Non-Oxidizable (stable) C in four different land use systems, namely Monoculture (Brachiaria grassland), Association (Brachiaria + Arachis pintoi), Forage Bank (a mixture of forage tree species), and Natural Regeneration of the pasture in both a flat area and a sloping one. The Degraded Pasture was the reference.Results showed that in the sloping area all treatments have higher Total Carbon stocks than the Degraded Pasture, while three of the treatments significantly increased the stocks of Non-Oxidizable C.In the flat landscape, only the Association significantly increased Total C stocks. Plowing and fertilization cause significant increases in Oxidizable carbon and decreases in Non-Oxidizable carbon. This effect needs further research, as C stability will influence equilibrium stocks.In the sloping area, improved pastures and fodder bank rapidly increased Total Carbon contents and stocks, with increases as large as10 ton.ha^?1 yr^?1. In the Traditional Fodder Bank, which showed the largest increase, this is partially due to the application of organic manure. Surprisingly, also C stocks under Natural Regeneration were significantly higher than under the original Degraded Grassland. This increase was fully due to Non-Oxidizable Carbon, which is difficult to explain.Stable isotope analysis indicated that under improved grassland, especially Brachiaria monoculture, up to 40% of the original C in the upper 10 cm was replaced in 3.3 years.     

Changes in enzyme activities and microbial biomass after “in situ” remediation of a heavy metal-contaminated soil

Microbial properties such as microbial biomass carbon (MBC), arylsulfatase, β-glucosidase and dehydrogenase activities, and microbial heterotrophic potential, together with several chemical properties such as pH, CaCl₂ soluble heavy metal concentrations, total organic carbon and hydrosoluble carbon were measured to evaluate changes in soil quality, after “in situ” remediation of a heavy metal-contaminated soil from the Aznalcóllar mine accident (Southern Spain, 1998). The experiment was carried out using containers, filled with soil from the affected area. Four organic amendments (a municipal waste compost, a biosolid compost, a leonardite and a litter) and an inorganic amendment (sugarbeet lime) were mixed with the top soil at the rate of 100 Mg ha⁻¹. Unamended soil was used as control. Agrostis stolonifera L. was sown in the containers. The soil was sampled twice: one month and six months after amendment application. In general, these amendments improved the soil chemical properties: soil pH, total organic carbon and hydrosoluble carbon increased in the amended soils, while soluble heavy metal concentrations diminished. At the same time, higher MBC, enzyme activities and maximum rate of glucose mineralization values were found in the organically amended soils. Plant cover was also important in restoring the soil chemical and microbial properties in all the soils, but mainly in those that were not amended organically. As a rule, remediation measures improved soil quality in the contaminated soils.     

Long-term effects of land use and fertiliser treatments on sulphur transformations in soils from the Broadbalk experiment

Sulphur transformations were monitored in a unique set of arable, grassland and woodland soils from the Broadbalk Classical Experiment, which started in 1843. In an open incubation experiment with periodic leaching, 14–35 mg SO₄²⁻-S kg⁻¹ was mineralised in 28 weeks at 25°C, equivalent to 4.4–8.3% soil organic S. Cumulative amounts of S mineralised increased linearly during the 28 weeks, indicating constant rates of mineralisation. The rate of mineralisation was the greatest in the woodland soil (170 μg SO₄-S kg⁻¹ day⁻¹), followed by the grassland (120 μg SO₄-S kg⁻¹ day⁻¹) and the arable soil from the farmyard manure (FYM) plot (110 μg SO₄-S kg⁻¹ day⁻¹). Three soils from arable plots receiving different inorganic fertiliser treatments but no FYM had similar rates of S mineralisation (~70 μg SO₄-S kg⁻¹ day⁻¹). In an incubation experiment with ³⁵SO₄²⁻, addition of glucose greatly enhanced S immobilisation. In 132 days, the woodland and grassland soils immobilised more S than the arable soils, with or without glucose amendment. Immobilisation and mineralisation of S occurred concurrently, and both were stimulated by glucose addition. The results show that S mineralisation and immobilisation were influenced strongly by the type of land-use and long-term organic manuring, whereas annual application of sulphate-containing fertilisers for over 150 years had few effects on short-term S transformations.     

Changes in soil microbial biomass and functional diversity with a nitrogen gradient in soil columns

Fertilization generates nutrient patches that may impact soil microbial activity. In this study, nitrogen patches were generated by adding ammonium sulfate or urea to soil columns (length 25 cm; internal diameter 7.2 cm). Changes in nitrogen transformation, soil microbial biomass, and microbial functional diversity with the nitrogen gradients were investigated to evaluate the response of microbial activity to chemical fertilizer nutrient patches. After applying of ammonium sulfate or urea, the added nitrogen migrated about 7 cm. Microbial biomass carbon (MBC) was lower in fertilized soil than in the control (CK) treatment at the same soil layers. MBC increased with soil depth while microbial biomass nitrogen (MBN) decreased. BIOLOG analysis indicated that the average well color development (AWCD) and functional diversity indices of the microbial communities were lower in the 1 cm and 2 cm soil layers after application of ammonium sulfate; the highest values were in the 3 cm soil layer. AWCD and Shannon indices from the 1 to 5 cm soil layers were higher than those from other soil layers under urea application. Both principal component analysis and carbon substrate utilization analysis showed significant separation of soil microbial communities among different soil layers under application of ammonium sulfate or urea. Microbial activity was substantially decreased when NH₄⁺-N concentration was higher than 528.5 mg kg⁻¹ (1–3 cm soil layer under ammonium sulfate application) or 536.8 mg kg⁻¹ (1 cm soil layer under urea application). These findings indicated that changes in soil microbial biomass and microbial functional diversity can occur with a nitrogen gradient. The extent of changes depends on the nitrogen concentration and the form of inorganic fertilizer.     

Factors causing temporal and spatial variation in heterotrophic and rhizospheric components of soil respiration in afforested organic soil croplands in Finland

Partitioning soil respiration (SR) into its components, heterotrophic and rhizospheric respiration, is an important step for understanding and modelling carbon (C) cycling in organic soils. However, no partitioning studies on afforested organic soil croplands exist. We separated soil respiration originating from the decomposition of peat (SR_P), and aboveground litter (SR_L) and root respiration (SR_R) in six afforested organic soil croplands in Finland with varying tree species and stand ages using the trenching method. Across the sites temporal variation in SR was primarily related to changes in soil surface temperature (?5 cm), which explained 71–96% of variation in SR rates. Decomposition of peat and litter was not related to changes in water table level, whereas a minor increase in root respiration was observed with the increase in water table depth. Temperature sensitivity of SR varied between the different respiration components: SR_P was less sensitive to changes in soil surface temperature than SR_L or SR_R. Factors explaining spatial variation in SR differed between different respiration components. Annual SR_P correlated positively with peat ash content while that of SR_L was found to correlate positively with the amount of litter on the forest floor, separately for each tree species. Root respiration correlated positively with the biomass of ground vegetation. From the total soil respiration peat decomposition comprised a major share of 42%; the proportion of autotrophic respiration being 41% and aboveground litter 17%. Afforestation lowered peat decomposition rates. Nevertheless the effect of agricultural history can be seen in peat properties for decades and due to high peat decomposition rates these soils still loose carbon to the atmosphere.     

Soil organic carbon and nitrogen in a Mollisol in central Ohio as affected by tillage and land use

Minimum tillage practices are known for increasing soil organic carbon (SOC). However, not all environmental situations may manifest this potential change. The SOC and N stocks were assessed on a Mollisol in central Ohio in an 8-year-old tillage experiment as well as under two relatively undisturbed land uses; a secondary forest and a pasture on the same soil type. Cropped systems had 51±4 (equiv. mass) Mg ha⁻¹ lower SOC and lower 3.5±0.3 (equiv. mass) Mg ha⁻¹ N in the top 30 cm soil layer than under forest. Being a secondary forest, the loss in SOC and N stocks by cultivation may have been even more than these reported herein. No differences among systems were detected below this depth. The SOC stock in the pasture treatment was 29±3 Mg ha⁻¹ greater in the top 10 cm layer than in cultivated soils, but was similar to those under forest and no-till (NT). Among tillage practices (plow, chisel and NT) only the 0–5 cm soil layer under NT exhibited higher SOC and N concentrations. An analysis of the literature of NT effect on SOC stocks, using meta-analysis, suggested that NT would have an overall positive effect on SOC sequestration rate but with a greater variability of what was previously reported. The average sequestration rate of NT was 330 kg SOC ha⁻¹ year⁻¹ with a 95% confidence interval ranging from 47 to 620 kg SOC ha⁻¹ year⁻¹. There was no effect of soil texture or crop rotation on the SOC sequestration rate that could explain this variability. The conversion factor for SOC stock changes from plow to NT was equal to 1.04. This suggests that the complex mechanisms and pathways of SOC accrual warrant a cautious approach when generalizing the beneficial changes of NT on SOC stocks.     

Micro-scale modelling of carbon turnover driven by microbial succession at a biogeochemical interface

The detritusphere is a very thin but microbiological highly active zone in soil. To trace the fate of litter carbon in the detritusphere we developed a new 1D dynamic mechanistic model. In a microcosm experiment soil cores were incubated with ¹³C labelled rye residues (δ¹³C=299‰), which were placed on the surface. Microcosms were sampled after 3, 7, 14, 28, 56 and 84 days and soil cores were separated into layers of increasing distance to the litter. Gradients in soil organic carbon (TOC), dissolved organic carbon (DOC), microbial biomass and activity were detected over a distance of 3 mm from the litter layer. The newly developed 1D model simulates both the total carbon and the ¹³C carbon pools and fluxes, so that it was possible to include the ¹³C data in model optimisation. The special feature of the model is that it operates with two decomposer populations; the first one is assumed to be dominated by bacteria (initial-stage decomposer) and second one by fungi (late-stage decomposer). Moreover, in the model the DOC pool is divided into two sub pools. Each DOC pool is consumed by one of the decomposer populations. After parameter optimisation the model was well suited to simulate the experimental data. The model explained 92% of the observed variance. The model output provides a comprehensive insight into the carbon cycling within the detritusphere. The simulation results showed among others that after 84 days about 10% of total litter C was transferred to the soil organic matter (SOM) pool. Only 3% was located in the microbial biomass. From the evolved CO₂ 71% was litter-derived and 29% was soil-derived. From the litter-derived CO₂, 69% was directly formed in the litter layer. The remaining 31% was transported to soil before mineralisation. Our study shows that a combination of experimental work and mathematical modelling is a powerful approach to provide a comprehensive insight into the small-scale carbon turnover in soil.     

Litter, warming and plants affect respiration and allocation of soil microbial and plant C, N and P in arctic mesocosms

In a mesocosm experiment, we studied decomposition rates as CO₂ efflux and changes in plant mass, nutrient accumulation and soil pools of nitrogen (N) and phosphorus (P), in soils from a sub-arctic heath. The soil was incubated at 10 °C and 12 °C, with or without leaf litter and with or without plants present. The purpose of the experiment was to analyse decomposition and nutrient transformations under simulated, realistic conditions in a future warmer Arctic.Both temperature enhancement and litter addition increased respiration rates. Temperature enhancement and surprisingly also litter addition decreased microbial biomass carbon (C) content, resulting in a pronounced increase of specific respiration. Microbial P content increased progressively with temperature enhancement and litter addition, concomitant with increasing P mineralisation, whereas microbial N increased only in the litter treatment, at the same time as net N mineralisation decreased. In contrast, microbial biomass N decreased as temperature increased, resulting in a high mobilisation of inorganic N.Plant responses were closely coupled to the balance of microbial mineralisation and immobilisation. Plant growth and N accumulation was low after litter addition because of high N immobilisation in microbes and low net mineralisation, resulting in plant N limitation. Growth increased in the temperature-enhanced treatments, but was eventually limited by low supply of P, reflected in a low plant P concentration and high N-to-P ratio. Hence, the different microbial responses caused plant N limitation after litter addition and P limitation after temperature enhancement. Although microbial processes determined the main responses in plants, the plants themselves influenced nutrient turnover. With plants present, P mobilisation to the plant plus soil inorganic pools increased significantly, and N mobilisation non-significantly, when litter was added. This was presumably due to increased mineralisation in the rhizosphere, or because the nutrients in addition to being immobilised by microbes also could be absorbed by plants. This suggests that the common method of measuring nutrient mineralisation in soils incubated without plants may underestimate the rates of nutrient mobilisation, which probably contributes to a commonly observed discrepancy of measured lower rates of net nutrient mineralisation than uptake rates in arctic soils.     

Vertical distribution of microbial communities under the canopy of two legume bushes in the Tehuacán Desert,Mexico

Prosopis laevigata and Parkinsonia praecox are the most abundant perennial shrubs in the Tehuacán Desert, forming ’islands of fertility’ that dominate the alluvial terraces. Both species exhibit very similar phenology, with the timing of litter foliage being the only difference between them. P. praecox litter occurs shortly after the rains, while P. laevigata maintains its leaves until the next wet season. As degradable organic matter (OM) is one of the leading factors determining soil biota composition and activity, because of the OM provided by littering, we expected that the vertical distribution of the microbial community in the vicinity of the root zone of P. praecox would be higher in comparison to P. laevigata. One soil sampling was performed; during the rainy season in August, soil samples were collected from a 0–50-cm depth at 10-cm intervals, in the vicinity of the root canopy of four individual plants of each species and the interspaces between them. Soil moisture, organic matter, and counts of bacteria and fungi under shrubs were found to decrease from the upper to deeper layers. Respiratory activity was higher in the deeper layers (p < 0.01) in all three sampling sites. Total bacterial, fungal, and heterotrophic diazotrophs were found to be significantly (p < 0.001) more numerous under shrubs than in the interspace soil. No nitrogen-fixing bacteria were isolated from interplant soils in comparison to the soil samples collected beneath the shrubs. Heterotrophic diazotrophs significantly (p < 0.01) reduced more acetylene under P. praecox (29.0 nmol/g soil) than under P. laevigata (20.1 nmol/g soil). Although the microbial numbers were unaffected by differences in plant phenology, greater nitrogenase activity under P. praecox may influence nitrogen distribution in this arid environment. Due to the fact that only one sampling was undertaken, this study elucidates the differences in the microbial community between the two shrubs, but the dynamics in the above community could not be shown.     

Winter wheat carbon exchange in Thuringia,Germany

Eddy covariance measurements and estimates of biomass net primary production (NPP) in combination with soil carbon turnover modelled by the Roth-C model were used to assess the ecosystem carbon balance of an agricultural ecosystem in Thuringia, Germany, growing winter wheat in 2001. The eddy CO₂ flux measurements indicate an annual net ecosystem exchange (NEE) uptake in the range from −185 to −245 g C m⁻² per year. Main data analysis uncertainty in the annual NEE arises from night-time u¹ screening, other effects (e.g. coordinate rotation scheme) have only a small influence on the annual NEE estimate. In agricultural ecosystems the fate of the carbon removed during harvest plays a role in the net biome production (NBP) of the ecosystem, where NBP is given by net ecosystem production (NEP=−NEE) minus non-respiratory losses of the ecosystem (e.g. harvest). Taking account of the carbon removed by the wheat harvest (290 g C m⁻²), the agricultural field becomes a source of carbon with a NBP in the order of −45 to −105 g C m⁻² per year. Annual carbon balance modelled with the Roth-C model also indicated that the ecosystem was a source for carbon (NBP −25 to −55 g C m⁻² per year). Based on the modelling most of carbon respired resulted from changes in the litter and fast soil organic matter pool. Also, the crop and management history, particularly the C input to soil in the previous year, significantly affect next year’s CO₂ exchange.     

Comparison of forest soil carbon dynamics at five sites along a latitudinal gradient

The aim of this study was to compare the turnover time of labile soil carbon (C), in relation to temperature and soil texture, in several forest ecosystems that are representative of large areas of North America. Carbon and nitrogen (N) stocks, and C:N ratios, were measured in the forest floor, mineral soil, and two mineral soil fractions (particulate and mineral-associated organic matter, POM and MOM, respectively) at five AmeriFlux sites along a latitudinal gradient in the eastern United States. Sampling at four sites was replicated over two consecutive years. With one exception, forest floor and mineral soil C stocks increased from warm, southern sites (with fine-textured soils) to cool, northern sites (with more coarse-textured soils). The exception was a northern site, with less than 10% silt-clay content, that had a soil organic C stock similar to the southern sites. A two-compartment model was used to calculate the turnover time of labile soil organic C (MRT_U) and the annual transfer of labile C to stable C (k₂) at each site. Moving from south to north, MRT_U increased from approximately 5 to 14 years. Carbon-13 enrichment factors (ε), that described the rate of change in δ¹³C through the soil profile, were associated with soil C turnover times. Consistent with its role in stabilization of soil organic C, silt-clay content was positively correlated (r = 0.91; P ≤ 0.001) with parameter k₂. Latitudinal differences in the storage and turnover of soil C were related to mean annual temperature (MAT, °C), but soil texture superseded temperature when there was too little silt and clay to stabilize labile soil C and protect it from decomposition. Each site had a relatively high proportion of labile soil C (nearly 50% to a depth of 20 cm). Depending on unknown temperature sensitivities, large labile pools of forest soil C are at risk of decomposition in a warming climate, and losses could be disproportionately higher from coarse textured forest soils.     

Organic carbon sequestration in earthworm burrows

Earthworms strongly affect soil organic carbon cycling. The aim of this study was to determine whether deep burrowing anecic earthworms enhance carbon storage in soils and decrease C turnover. Earthworm burrow linings were separated into thin cylindrical sections with different distances from the burrow wall to determine gradients from the burrow wall to the surrounding soil. Organic C, total N, radiocarbon (¹⁴C) concentration, stable isotope values (δ¹³C, δ¹⁵N) and extracellular enzyme activities were measured in these samples. Anecic earthworms increased C stocks by 270 and 310 g m^?2 accumulated in the vertical burrows. C-enrichment of the burrow linings was spatially highly variable within a distance of millimetres around the burrow walls. It was shown that C accumulation in burrows can be fast with C sequestration rates of about 22 g C m^?2 yr^?1 in the burrow linings, but accumulated C in the burrows may be mineralised fast with turnover times of only 3–5 years. Carbon stocks in earthworm burrows strongly depended on the earthworm activity which maintains continuous C input into the burrows. The enhanced extracellular enzyme activity of fresh casts was not persistent, but was 47% lower in inhabited burrows and 62% lower in abandoned burrows. Enzyme activities followed the C concentrations in the burrows and were not further suppressed due to earthworms. Radiocarbon concentrations and stable isotopes in the burrow linings showed an exponential gradient with the youngest and less degraded organic matter in the innermost part of the burrow wall. Carbon accumulation by anecic earthworm is restricted to distinct burrows with less influence to the surrounding soil. Contrary to the initial hypothesis, that organic C is stabilised due to earthworms, relaxation time experiments with nuclear magnetic resonance spectroscopy (NMR) did not reveal any enhanced adsorption of C on iron oxides with C stabilising effect. Our results suggest that earthworm activity does not substantially increase subsoil C stocks but burrows serve as fast ways for fresh C transport into deep soil horizons.     

Influence of temperature and vegetation cover on soluble inorganic and organic nitrogen in a spodosol

In this study, the influence of temperature and vegetation cover on soluble inorganic and organic nitrogen in a spodosol from north east Scotland was investigated. Firstly, soil cores were incubated at 5, 10 and 15°C for up to 8 weeks. Net mineralisation was observed at all temperatures with larger rates observed at higher temperatures. In contrast, water extractable dissolved organic nitrogen (DON) displayed no clear trend with time and showed little response to temperature. Secondly, intact cores of the same soil, with and without vegetation, were leached with artificial rain for 6 weeks at 6.5 and 15°C. Temperature and the presence of vegetation interacted to have a significant (P<0.01) effect on the concentration of NO₃⁻ in leachates; highest concentrations were observed in leachates from cores without vegetation at 15°C, whereas lowest concentrations were observed in leachates from cores with vegetation at 6.5°C. In contrast, concentrations of DON and dissolved organic carbon (DOC) were significantly (P<0.001) higher in leachates from cores with vegetation than without vegetation and were not affected by temperature. The cumulative amounts of DON and DOC leached from the cores with vegetation were 4 and 2.5 times greater, respectively, than those leached from the cores without vegetation. Comparison of soil solution (extracted by centrifugation at 0–5 and 5–10 cm depth) after leaching for 6 weeks, showed that the upper layer contained more than twice the amount of DON than the 5–10 cm layer and that the difference in concentration between the two depths was enhanced in the presence of vegetation. The results indicate that vegetation is an important source of DON and DOC. However, the removal of vegetation did not lead to an increase in the quantity of total dissolved nitrogen (TDN) in soil water, but resulted in a change in the dominant N fraction from DON to NO₃⁻. In addition, the results show that DON, in both the incubated and leached cores, did not change as inorganic N was mineralised. This suggests that if water extractable DON was acting as a source of NH₄⁺ or NO₃⁻, then it was being replenished by, and in equilibrium with, a large reserve of organic N. Evidence of such a pool was indirect in the form of additional DON (equivalent to 2 g N m⁻²) being extracted by 0.5 M K₂SO₄.