CARBON BUDGET AND SEQUESTRATION POTENTIAL IN A SANDY SOIL TREATED WITH COMPOST

The effects of compost application on soil carbon sequestration potential and carbon budget of a tropical sandy soil was studied. Greenhouse gas emissions from soil surface and agricultural inputs (fertiliser and fossil fuel uses) were evaluated. The origin of soil organic carbon was identified by using stable carbon isotope. The CO₂, CH₄ and N₂O emissions from soil were estimated in hill evergreen forest (NF) plot as reference, and in the corn cultivation plots with compost application rate at 30 Mg ha⁻¹ y⁻¹ (LC), and at 50 Mg ha⁻¹ y⁻¹ (HC). The total C emissions from soil surface were 8·54, 10·14 and 9·86 Mg C ha⁻¹ y⁻¹ for NF, HC and LC soils, respectively. Total N₂O emissions from HC and LC plots (2·56 and 3·47 kg N₂O ha⁻¹ y⁻¹) were significantly higher than from the NF plot (1·47 kg N₂O ha⁻¹ y⁻¹). Total CO₂ emissions from fuel uses of fertiliser, irrigation and machinery were about 10 per cent of total CO₂ emissions. For soil carbon storage, since 1983, it has been increased significantly (12 Mg ha⁻¹) under the application of 50 Mg ha⁻¹ y⁻¹ of compost but not with 30 Mg ha⁻¹ y⁻¹. The net C budget when balancing out carbon inputs and outputs from soil for NF, HC and LC soils were +3·24, −2·50 and +2·07 Mg C ha⁻¹ y⁻¹, respectively. Stable isotope of carbon (δ¹³C value) indicates that most of the increased soil carbon is derived from the compost inputs and/or corn biomass. Copyright © 2011 John Wiley & Sons, Ltd.     

Kinetics of glucose uptake by soil microorganisms

The kinetics of glucose uptake by soil microorganisms was investigated. Soil amended with an inorganic nutrient solution containing C glucose at concentrations of 2.5, 5.0, 10.0 or 20.0 mmol 1⁻¹ was maintained at 4, 12 or 25°C for varying times. The soil was analyzed for glucose, soluble ^14C, total organic ¹⁴C and evolved ¹⁴CO₂ to develop a carbon balance for the system and to define Michaelis-Menten kinetic parameters (K_m and V_max) for glucose uptake at each temperature.Glucose uptake rates, as measured by the depletion of glucose or soluble ¹⁴C from solution, were similar in soils maintained at 12 or 25°C. Based on the depletion of soluble ¹⁴C, values for K_m were 2.25 and 2.43 mmol I⁻¹ at 12 and 25°C, respectively, while V_max values were 0.25 and 1.61 h¹⁴', respectively. Glucose depletion at 4°C was faster than at 12C, while soluble ¹⁴C was removed at a significantly slower rate, suggesting soluble-C intermediates were produced in the 4°C system. Based on Chromatographie techniques and GC-MS, a soluble ¹⁴C-compound accumulating in the 4°C system was identified as maltose. The conversion of glucose to maltose resulted in K_m and V_max values of 17.29 mmol I⁻¹ and 0.12h⁻¹, respectively, for soluble ¹⁴C depletion and 4.96mmol1⁻¹ and 0.43 h⁻, respectively, for glucose depletion at 4δC. These results demonstrate the need to differentiate uptake rates for the parent compound as well as for transitory intermediates excreted into the growth medium. Evolution of CO₂ was shown to be a poor indicator of the rapid disappearance of glucose in soils.     

Denitrification characteristics of subtropical soils in China affected by soil parent material and land use

Forty‐five soil samples were collected from rice paddy land (R), tea garden land (T), forestland (F), brush land (B), and upland (U) in Jiangxi province, a subtropical region of China. These soils were derived from Quaternary red earth (Q), Tertiary red sandstone (S), and granite (G). Their denitrification capacities were determined after treatment with 200 mg NO₃⁻‐N kg⁻¹ soil by measuring changes in NO₃⁻‐N content during a 28‐day anaerobic incubation under N₂ gas in the headspace, at 30°C. The subtropical soils studied here were characterized by generally small denitrification capacities, ranging from no denitrification capacity to complete disappearance of added NO₃⁻‐N within 11 days of incubation. With few exceptions, NO₃⁻‐N reduction with incubation time followed a first‐order relationship with reaction constants of 0 – 0.271 day⁻¹, but the data could be simulated better by a logarithmic relationship. Thus, denitrification capacity was determined by the reaction constant of the first‐order reaction, the slope of the logarithmic relationship, and the averaged NO₃⁻‐N reduction rate in the first 7 days of anaerobic incubation (ranging from 0 to 28.5 mg kg⁻¹day⁻¹), and was significantly larger in the soils derived from G than from Q and S for all land uses except for rice paddy land. Soil organic carbon and nitrogen availability are the key factors that determine differences in denitrification capacity among the three soil parent materials. Rice cultivation significantly promoted denitrification capacity compared with the other four land uses and masked the effect of soil parent materials on denitrification capacity. This is most likely due to increases in organic carbon and total N content in the soil, which promoted the population and biological activities of microorganisms which are able to respire anaerobically when the rice soil is flooded. Neither the increased pH of upland soil caused by the addition of lime for upland crop production, nor the decreased pH of the tea garden soil by the acidification effect of tea plants altered soil denitrification capacity. Our results suggest that land use and management practices favour soil carbon and/or nitrogen accumulation and anaerobic microorganism activities enhance soil denitrification capacity.     

Dissolved organic matter leaching in some contrasting New Zealand pasture soils

Leaching of dissolved organic matter (DOM) from pastoral soils is increasingly seen as an important but poorly understood process. This paper examined the relationship between soil chemical properties, microbial activity and the losses of dissolved organic carbon (DOC) and nitrogen (DON) through leaching from six pasture soils. These soils differed in carbon (C) (4.6–14.9%) and nitrogen (N) (0.4–1.4%) contents and in the amount of organic C and N that had accumulated or been lost in the preceding 20+ years (i.e. −5131 to +1624 kg C ha⁻¹ year⁻¹ and −263 to +220 kg N ha⁻¹ year⁻¹, respectively). The paper also examined whether between‐soil‐type differences in DOC and DON leaching was a major explanatory factor in the observed range of soil organic matter (SOM) changes in these soils. Between 280 and 1690 kg C ha⁻¹ year⁻¹ and 28–117 kg N ha⁻¹ year⁻¹ leached as DOC and DON, respectively, from the six soils in a lysimeter study, with losses being greater from two poorly drained gley soils. Losses of C and N of this magnitude, while at the upper end relative to published data, could not fully explain the losses at Rawerawe, Bruntwood and Lepperton sites reported by Schipper et al. (2007) . The study highlights the leaching of DOM as a significant pathway of loss of C and N in pasture soils that is often ignored or given little attention in predictive models and nutrient budgeting. Leaching losses of DOC and DON alone, or in combination with slightly increased respiration losses of SOM given a 0.2°C increase in the mean annual soil temperature, do not fully explain long‐term changes in the SOM observed at these sites. When soils examined in the present study were separated on the basis of drainage class, the losses of DOC by leaching were correlated with both total and hot‐water extractable C (HWC), the latter being a measure of the labile SOM fraction. Basal microbial CO₂ respiration rates, which varied between 1 and 3.5 µg CO₂‐C g⁻¹ soil hour⁻¹ in surface soils (0–75‐mm depth), was also linked to HWC and the quantities of C lost as DOC. Adoption of the HWC method as an approach that could be used as a proxy for the direct measurement of the soil organic C lost by leaching as DOC or respired needs to be examined further with a greater number of soils. In comparison, a poor relationship was found between the hot‐water extractable N (HWN) and loss of DON by leaching, despite HWN previously being shown to be a measure of the mineralizable pool of N in soils, possibly reflecting the greater competition for N than C in these soils.     

Throughfall Chemistry in a Sitka Spruce Plantation in Response to Six Different Simulated Polluted Mist Treatments

A mixed provenance Sitka spruce plantation, planted in 1986 on a drained deep peat, has been exposed to 6 different simulated mist treatments in 4 replicated blocks since 1996. Treatments provided N and/or S at a concentration of 1.6 mol m^?3, supplying ca. 50 kg S and/or N ha^?1 yr^?1 as N (NH₄NO₃), S (Na₂SO₄), NS Acid (NH₄NO₃ + H₂SO₄ at pH 2.5), 2NS Acid (double dose by application at twice frequency), a control treatment supplied with additional rainwater only and a 'no treatment' set of plots. Throughfall, preserved with thymol in the field, was collected using gutters with a surface area of 1 m² in all the replicate plots, and was analysed for all major ions. Prior to treatment in 1999, S deposition in throughfall exceeded that in rain because of dry deposition of SO₂ and SO₄ ^2? to the canopy; NH₄ ⁺ and NO₃ ^? ions were both retained in the canopy. During treatment, only 20–40% of the applied N in the high-N treatments was retained in the canopy. Acidity in the applied mist was partly neutralised by the canopy, but not primarily through exchange of base cations, leading to the conclusion that weak organic acids, in solution or in situ in the canopy, contributed to the buffering of the H⁺ ion deposition in the acid treatments.     

Carbon Life Cycle Assessment for Prairie as a Crop in Reclaimed Mine Land

A life cycle assessment with carbon (C) as the reference unit was used to balance the benefits of land preparation practices of establishing tall‐grass prairies as a crop for reclaimed mine land with reduced environmental damage. Land preparation and management practices included disking with sub‐soiling (DK‐S), disking only (DK), no tillage (NT), and no tillage with grazing (NT‐G). To evaluate the C balance and energy use of each of the land preparations, an index of sustainability (I_s = C_O/C_I, Where: C_O is the sum of all outputs and C_I is the sum of all inputs) was used to assess temporal changes in C. Of the four land preparation and management practices, DK had the highest I_s at 8·53. This was due to it having the least degradation of soil organic carbon (SOC) during land‐use change (−730 kg ha⁻¹ y⁻¹) and second highest aboveground biomass production (9,881 kg ha⁻¹). The highest aboveground biomass production occurred with NT (11,130 kg ha⁻¹), although SOC losses were similar to DK‐S, which on average was 2,899 kg ha⁻¹ y⁻¹. The I_s values for NT and DK‐S were 2·50 and 1·44, respectively. Grazing from bison reduced the aboveground biomass to 8,971 kg ha⁻¹ compared with NT with no grazing, although stocking density was low enough that I_s was still 1·94. This study has shown that converting from cool‐season forage grasses to tall‐grass prairie results in a significant net sink for atmospheric CO₂ 3 years after establishment in reclaimed mine land, because of high biomass yields compensating for SOC losses from land‐use change. Copyright © 2014 John Wiley & Sons, Ltd.     

Tea plantation destroys soil retention of NO3− and increases N2O emissions in subtropical China

The intensive conversion from woodland to tea plantation in subtropical China might significantly change the potential supply processes and cycling of inorganic Nitrogen (N). However, few studies have been conducted to investigate the internal N transformations involved in the production and consumption of inorganic N and N₂O emissions in subtropical soils under tea plantations. In a ¹⁵N tracing experiment, nine tea fields with different plantation ages (1-y, 5-y and 30-y) and three adjacent woodlands were sampled to investigate changes in soil gross N transformation rates in humid subtropical China. Conversion of woodland to tea plantation significantly altered soil gross N transformation rates. The mineralization rate (M_Norg) was much lower in soils under tea plantation (0.53–0.75 mg N kg⁻¹ d⁻¹) than in soil sampled from woodland (1.71 mg N kg⁻¹ d⁻¹), while the biological inorganic N supply (INS), defined as the sum of organic N mineralized into NH₄⁺ (M_Norg) and heterotrophic nitrification (O_Nrec), was not significantly different between soils under woodland and tea plantation, apart from soil under 30-y tea plantation which had the largest INS. Interestingly, the contribution of O_Nrec to INS increased from 19.6% in soil under woodland to 65.0–82.4% in tea-planted soils, suggesting O_Nrec is the dominant process producing inorganic N in tea-planted soils. Meanwhile, the conversion from woodland to tea plantation destroyed soil NO₃⁻ retention by increasing O_Nrec, autotrophic nitrification (O_NH4) and abiotic release of stored NO₃⁻ while decreasing microbial NO₃⁻ immobilization (I_NO3), resulting in greater NO₃⁻ production in soil. In addition, long-term tea plantation significantly enhanced the potential release of N₂O. Soil C/N was positively correlated with M_Norg and I_NO3, suggesting that an increase in soil C/N from added organic materials (e.g. rice hull) is likely to reduce the increased production of NO₃⁻ in the soils under tea plantation.     

Mulching Affects Soil Properties and Greenhouse Gas Emissions Under Long‐Term No‐Till and Plough‐Till Systems in Alfisol of Central Ohio

Agricultural activities emit greenhouse gases (GHGs) and contribute to global warming. Intensive plough tillage (PT), use of agricultural chemicals and the burning of crop residues are major farm activities emitting GHGs. Intensive PT also degrades soil properties by reducing soil organic carbon (SOC) pool. In this scenario, adoption of no‐till (NT) systems offers a pragmatic option to improve soil properties and reduce GHG emission. We evaluated the impacts of tillage systems (NT and PT) and wheat residue mulch on soil properties and GHG emission. This experiment was started in 1989 on a Crosby silt loam soil at Waterman Farm, The Ohio State University, Columbus, Ohio, USA. Mulching reduced soil bulk density and improved total soil porosity. More total carbon (16.16 g kg⁻¹), SOC (8.36 mg L⁻¹) and soil microbial biomass carbon (152 µg g⁻¹) were recorded in soil under NT than PT. Mulch application also decreased soil temperature (0–5 cm) and penetration resistance (0–60 cm). Adoption of long‐term NT reduced the GHG emission. Average fluxes of GHGs under NT were 1.84 g CO₂‐C m⁻² day⁻¹ for carbon dioxide, 0.07 mg CH₄‐C m⁻² day⁻¹ for methane and 0.73 mg N₂O‐N m⁻² day⁻¹ for nitrous oxide compared with 2.05 g CO₂‐C m⁻² day⁻¹, 0.74 mg CH₄‐C m⁻² day⁻¹ and 1.41 mg N₂O‐N m⁻² day⁻¹, respectively, for PT. Emission of nitrous oxide was substantially increased by mulch application. In conclusion, long‐term NT reduced the GHG emission by improving the soil properties. Copyright © 2016 John Wiley & Sons, Ltd.     

Modelling soil compaction impacts on nitrous oxide emissions in arable fields

Nitrous oxide (N₂O) emissions comprise the major share of agriculture's contribution to greenhouse gases; however, our understanding of what is actually happening in the field remains incomplete, especially concerning the multiple interactions between agricultural practices and N₂O emissions. Soil compaction induces major changes in the soil structure and the key variables controlling N₂O emissions. Our objective was to analyse the ability of a process‐based model (Nitrous Oxide Emissions (NOE)) to simulate the impact of soil compaction on N₂O emission kinetics obtained from field experiments. We used automatic chambers to continuously monitor N₂O and CO₂ emissions on uncompacted and compacted areas in sugar beet fields during 2 years. Soil compaction led to smaller CO₂ emissions and larger N₂O emissions by inducing anoxic conditions favourable for denitrification. Cumulative N₂O emissions during the crop cycles were 944 and 977 g N ha⁻¹ in uncompacted plots and 1448 and 1382 g N ha⁻¹ in compacted plots in 2007 and 2008, respectively. The NOE model ( Hénault et al., 2005 ) simulated 106 and 138 g N₂O‐N ha⁻¹ in uncompacted plots and 1550 and 650 g N₂O‐N ha⁻¹ in compacted plots in 2007 and 2008, respectively, markedly under‐estimating the nitrification rates and associated N₂O emissions. We modified the model on the basis of published results in order to better simulate nitrification and account for varying N₂O fractions of total end‐products in response to varying soil water and nitrate contents. The modified model (NOE2) better predicted nitrification rates and N₂O emissions following fertilizer addition. Using a fine vertical separation of soil layers of configurable, but constant, thickness (1 cm) also improved the simulations. NOE2 predicted 428 and 416 g N‐N₂O ha⁻¹ in uncompacted plots and 1559 and 1032 g N‐ N₂O ha⁻¹ in compacted plots in 2007 and 2008, respectively. These results show that a simple process‐based model can be used to predict successfully the post‐fertilizer addition kinetics of N₂O emissions and the impact of soil compaction on these emissions. However, large emissions later on during the cropping cycle were not captured by the model, emphasizing the need for further research.     

CARBON FIXATION OF CYANOBACTERIAL–ALGAL CRUSTS AFTER DESERT FIXATION AND ITS IMPLICATION TO SOIL ORGANIC CARBON ACCUMULATION IN DESERT

Enhanced carbon fixation in soil crusts may facilitate the restoration of damaged ecosystems, but this requires greater knowledge of carbon fixation patterns and mechanisms. We measured the net photosynthetic rate (P_n) and estimated annual carbon fixation (ACF) in cyanobacterial–algal crusts after desert fixation in the Tengger Desert, northwestern China. The accumulated carbon fixation since the establishment of a restoration site was also calculated. In addition, stepwise regression analysis was used to study the relation between P_n and ACF and the physicochemical properties of crusts. Results showed that P_n was significantly higher at a more established 51‐year‐old restoration site (1·57 µmol m⁻² s⁻¹) than at a younger 15‐year‐old site (0·92 µmol m⁻² s⁻¹). The ACF also increased significantly with restoration time, but in two temporal phases, a slower ACF phase between 15 and 26 years of restoration (0·28–0·7 gC m⁻² y⁻¹) and a high ACF phase after 43–51 years of restoration (3·3 gC m⁻² y⁻¹). Stepwise regression analysis revealed that P_n was significantly correlated with chlorophyll a and crust cover, whereas ACF was only correlated with crust cover. Accumulated carbon fixation increased from 2·9 gC m⁻² after 15 years to 35·4 gC m⁻² at 51 years following establishment of the restoration site. The accumulated carbon fixation was positively correlated with soil organic carbon content. This study demonstrated that carbon fixation by cyanobacterial–algal crusts increased progressively after desert fixation. Artificial measures, like the establishment of these restoration zones, can facilitate the colonization and development of biological soil crusts and are an effective biological tool for desert soil restoration. Copyright © 2011 John Wiley & Sons, Ltd.     

Implication of Gypsum Rates to Optimize Hydraulic Conductivity for Variable‐Texture Saline–Sodic Soils Reclamation

Sodium (Na⁺) dominated soils reduce saturated hydraulic conductivity (K_s) by clay dispersion and plugging pores, while gypsum (CaSO₄•2H₂O) application counters these properties. However, variable retrieval of texturally different saline–sodic soils with gypsum at soil gypsum requirement (SGR) devised to define its quantity best suited to improve K_s, leach Na⁺ and salts. This study comprised loamy‐sand (LS), sandy loam (SL), and clay loam (CL) soils with electrical conductivity of saturation extract (EC_e) of ~8 dS m⁻¹, sodium adsorption ratio (SAR) of ~44 (mmol L⁻¹)^1/2 and exchangeable sodium of ~41%, receiving no gypsum (G₀), gypsum at 25% (G₂₅), 50% (G₅₀) and 75% (G₇₅) of SGR. Soils packed in lysimeters were leached with low‐carbonate water [EC at 0·39 dS m⁻¹, SAR at 0·56 (mmol L⁻¹)^1/2 and residual sodium carbonate at 0·15 mmol_c L⁻¹]. It proved that a rise in gypsum rate amplified K_s of LS ≫ SL > CL. However, K_s of LS soil at G₂₅ and others at G₇₅ remained efficient for salts and Na⁺ removal. Retention of calcium with magnesium (Ca²⁺ + Mg²⁺) by LS and SL soils increased by G₅₀ and decreased in G₇₅, while in CL, it also increased with G₇₅. The enhanced Na⁺ leaching efficiency in LS soil with G₂₅ was envisaged by water stay for sufficient time to dissolve gypsum and exchange and leach out Na⁺. Overall, the superiority of gypsum for LS at G₂₅, SL at G₅₀ and CL at G₇₅ predicted cost‐effective soil reclamation with a decrease in EC_e and SAR below 0·97 dS m⁻¹ and 5·92 (mmol L⁻¹)^1/2, respectively. Copyright © 2015 John Wiley & Sons, Ltd.     

Long‐Term Durum Wheat‐Based Cropping Systems Result in the Rapid Saturation of Soil Carbon in the Mediterranean Semi‐arid Environment

Climate, soil physical–chemical characteristics, land management, and carbon (C) input from crop residues greatly affect soil organic carbon (SOC) sequestration. According to the concept of SOC saturation, the ability of SOC to increase with C input decreases as SOC increases and approaches a SOC saturation level. In a 12‐year experiment, six semi‐arid cropping systems characterized by different rates of C input to soil were compared for ability to sequester SOC, SOC saturation level, and the time necessary to reach the SOC saturation level. SOC stocks, soil aggregate sizes, and C inputs were measured in durum wheat monocropping with (Ws) and without (W) return of aboveground residue to the soil and in the following cropping systems without return of aboveground residue to soil: durum wheat/fallow (Wfall), durum wheat/berseem clover, durum wheat/barley/faba bean, and durum wheat/Hedysarum coronarium. The C sequestration rate and SOC content were lowest in Wfall plots but did not differ among the other cropping systems. The C sequestration rate ranged from 0.47 Mg C ha⁻¹ y⁻¹ in Ws plots to 0.66 Mg C ha⁻¹ y⁻¹ in W plots but was negative (−0.06 Mg C ha⁻¹ y⁻¹) in Wfall plots. Increases in SOC were related to C input up to a SOC saturation value; over this value, further C inputs did not lead to SOC increase. Across all cropping systems, the C saturation value for the experimental soil was 57.7 Mg ha⁻¹, which was reached with a cumulative C input of 15 Mg ha⁻¹. Copyright © 2015 John Wiley & Sons, Ltd.     

The effect of soil phosphorus on particulate phosphorus in land runoff

Accumulation of surplus phosphorus (P) in the soil and the resulting increased transport of P in land runoff contribute to freshwater eutrophication. The effects of increasing soil P (19–194 mg Olsen‐P (OP) kg⁻¹) on the concentrations of particulate P (PP), and sorption properties (Q_max, k and EPCo) of suspended solids (SS) in overland flow from 15 unreplicated field plots established on a dispersive arable soil were measured over three monitoring periods under natural rainfall. Concentrations of PP in plot runoff increased linearly at a rate of 2.6 μg litre⁻¹ per mg OP kg⁻¹ of soil, but this rate was approximately 50% of the rate of increase in dissolved P (< 0.45 μm). Concentrations of SS in runoff were similar across all plots and contained a greater P sorption capacity (mean + 57%) than the soil because of enrichment with fine silt and clay (0.45–20 μm). As soil P increased, the P enrichment ratio of the SS declined exponentially, and the values of P saturation (P_sat; 15–42%) and equilibrium P concentration (EPCo; 0.7–5.5 mg litre⁻¹) in the SS fell within narrower ranges compared with the soils (6–74% and 0.1–10 mg litre⁻¹, respectively). When OP was < 100 mg kg⁻¹, P_sat and EPCo values in the SS were smaller than those in the soil and vice‐versa, suggesting that eroding particles from soils with both average and high P fertility would release P on entering the local (Rosemaund) stream. Increasing soil OP from average to high P fertility increased the P content of the SS by approximately 10%, but had no significant (P > 0.05) effect on the P_sat, or EPCo, of the SS. Management options to reduce soil P status as a means of reducing P losses in land runoff and minimizing eutrophication risk may therefore have more limited effect than is currently assumed in catchment management.     

Comparison of the eddy covariance and automated closed chamber methods for evaluating nocturnal CO2 exchange in a Japanese cypress forest

Underestimation of nocturnal CO₂ respiration using the eddy covariance method under calm conditions remains an unsolved problem at many flux observation sites in forests. To evaluate nocturnal CO₂ exchange in a Japanese cypress forest, we observed CO₂ flux above the canopy (F_c), changes in CO₂ storage in the canopy (S_t) and soil, and trunk and foliar respiration for 2 years (2003–2004). We scaled these chamber data to the soil, trunk, and foliar respiration per unit of ground area (F_s, F_t, F_f, respectively) and used the relationships of F_s, F_t, and F_f with air or soil temperature for comparison with canopy-scale CO₂ exchange measurements (=F_c + S_t). The annual average F_s, F_t, and F_f were 714 g C m⁻² year⁻¹, 170 g C m⁻² year⁻¹, and 575 g C m⁻² year⁻¹, respectively. At small friction velocity (u_*), nocturnal F_c + S_t was smaller than F_s + F_t + F_f estimated using the chamber method, whereas the two values were almost the same at large u_*. We replaced F_c + S_t measured during calm nocturnal periods with a value simulated using a temperature response function derived during well-mixed nocturnal periods. With this correction, the estimated net ecosystem exchange (NEE) from F_c + S_t data ranged from −713 g C m⁻² year⁻¹ to −412 g C m⁻² year⁻¹ in 2003 and from −883 g C m⁻² year⁻¹ to −603 g C m⁻² year⁻¹ in 2004, depending on the u_* threshold. When we replaced all nocturnal F_c + S_t data with F_s + F_t + F_f estimated using the chamber method, NEE was −506 g C m⁻² year⁻¹ and −682 g C m⁻² year⁻¹ for 2003 and 2004, respectively.     

Changes in the amount and distribution of neutral monosaccharides of savanna soils after plantation of Pinus and Eucalyptus in the Congo

In the Congo, near Pointe-Noire, Pinus and Eucalyptus were planted on the savanna for 30 years. We have characterized the effects of this change on land-use on the composition of carbohydrates in whole soil and particle-size fractions of the soil. Carbohydrates represent variable proportions of the total soil organic carbon (TOC) of various particle size fractions. The largest proportions of sugar-C were found in the savanna soil with as much as 250 mg g⁻¹ TOC in the coarsest plant remains and approximately 190 mg g⁻¹ TOC in the finest organo-mineral fractions, whereas there was always less sugar in plantation soils. The monosaccharide xylose and mannose have different distributions: xylose appears to be the marker of the vegetal inheritance, whereas the dominance of mannose in the clay fraction bears the signature of current microbial sugar synthesis. The quantitative and qualitative evolution of the whole soil carbohydrates was studied as a function of plantation age. Carbohydrate-C represents 131 mg g⁻¹ of the soil organic carbon in the savanna soil, but decreases to an average value of 75 mg g⁻¹ in plantations more than 6 years old. This appears to be due mainly to the stimulation of the mineralization of the glucose, which represented 60% of the total sugars in savanna soil and only 45–48% in tree plantations. The ratio [arabinose + galactose + fucose]/[rhamnose + xylose], which is the largest in the oldest plantations, is significant for evaluating the replacement of carbohydrates of the original grass savanna by those of the trees.     

Effects of biochar addition on greenhouse gas emissions during freeze–thaw cycles in a black soil region,Northeast China

As global warming intensifies, the soil environment in middle to high latitudes will undergo more extensive and frequent freeze–thaw cycles (FTCs), which will significantly affect the carbon and nitrogen cycles of soil ecosystems and aggravate greenhouse gas (GHG) emissions. Biochar can increase soil organic carbon storage and mitigate climate change. To effectively control GHG emissions, soil supplemented with biochar at different application rates (0%, 2%, 4% and 6% [w/w]) under different numbers of FTCs (0, 3, 6, 9, and 12) was selected as the research object. The soil GHG emission characteristics in different experimental treatments and their relationships with soil physical and chemical properties were determined. Our results showed that N₂O and CO₂ emissions were promoted during FTCs, with values of 3.13–50.37 and 16.22–135.50 μg m⁻² h⁻¹, respectively. The order of N₂O and CO₂ emissions with respect to biochar application rate was as follows: 2% > 0% > 4% > 6%. CH₄ emissions were negative during FTCs, varying from −1.62 to −10.59 μg m⁻² h⁻¹, and negative CH₄ emissions were promoted by biochar. Correlation analysis showed that N₂O, CO₂ and CH₄ emissions were significantly correlated with pH, soil moisture and soil organic matter (SOM), total nitrogen (TN) and ${\mathrm{NH}}_4^{+}$–N contents (p < .01). The conceptual path model demonstrated that GHG emissions were significantly influenced by FTCs, moisture, SOM and biochar application rate. Our results indicate that the effects of FTCs on GHG emissions were greater than those of biochar application. Biochar application rates of 4% or 6% should be considered in the future to reduce soil GHG emissions in the black soil region of Northeast China. Our results can help provide a theoretical basis and effective strategy to reduce soil GHG emissions during FTCs in seasonally frozen regions.     

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.     

Evidence of dissolved trivalent manganese in acidic forest soils

Background

Evidence of trivalent manganese (Mn³⁺) in the aqueous phase of soils is unknown so far although this strong oxidant has large environmental implications.

Aims

We aimed to modify a spectrophotometric protocol (porphyrin method) and to discriminate between Mn²⁺ and Mn³⁺ in the aqueous phase of forest soils based on kinetic modeling.

Methods

We investigated manganese speciation in 12 forest floor solutions and 41 soil solutions from an acidic forest site by adjusting pH and correcting for absorbance.

Results

The solutions showed broad ranges in pH (3.4−6.3), dissolved organic carbon (DOC, 1.78−77.1 mg C L⁻¹), and total Mn (Mn_T, 23.9−908 µg L⁻¹). For acidic solutions, a pH-buffer was added to increase the pH of the solutions to 7.5−8.0, and background absorption was corrected for colored solutions, that is, solutions high in DOC. This was done to accelerate the reaction kinetics and avoid overestimation of Mn_T concentrations. After the pH and color adjustments, the comparison of Mn_T concentrations between the porphyrin method and optical emission spectrometry showed good agreement. Trivalent Mn, which is stabilized by organic ligands, constitutes significant proportions in both forest floor solutions (10−87%) and soil solutions (0.5−74%).

Conclusions

The dissolved Mn³⁺ is present in acidic forest soils. Thus, we revise the paradigm that this species is not stable and encourage to apply the revised method to other soils.     

Estimating diesel degradation rates from N2, O2 and CO2 concentration versus depth data in a loamy sand

The degradation rate of the pollutant is often an important parameter for designing and maintaining an active treatment system or for determining the rate of natural attenuation. A quasi‐steady‐state gas transport model based on Fick’s law with a correction term for advective flux, for estimating diesel degradation rates from N₂, O₂ and CO₂ concentration versus depth data, was evaluated in a laboratory column study. A loamy sand was spiked with diesel fuel at 0, 1000, 5000 and 10 000 mg kg⁻¹ soil (dry weight basis) and incubated for 15 weeks. Soil gas was sampled weekly at 6 selected depths in the columns and analysed for O₂, CO₂ and N₂ concentrations. The agreement between the measured and the modelled concentrations was good for the untreated soil (R²= 0.60) and very good for the soil spiked with 1000 mg kg⁻¹ (R²= 0.96) and 5000 mg kg⁻¹ (R²= 0.97). Oxygen consumption ranged from −0.15 to −2.25 mol O₂ m⁻³ soil day⁻¹ and CO₂ production ranged from 0.20 to 2.07 mol CO₂ m⁻³ soil day⁻¹. A significantly greater mean O₂ consumption (P < 0.001) and CO₂ production (P < 0.005) over time was observed for the soils spiked with diesel compared with the untreated soil, which suggests biodegradation of the diesel substrate. Diesel degradation rates calculated from respiration data were 1.5–2.1 times less than the change in total petroleum hydrocarbon content. The inability of this study to correlate respiration data to actual changes in diesel concentration could be explained by volatilization, long‐term sorption of diesel hydrocarbons to organic matter and incorporation of diesel hydrocarbons into microbial biomass, aspects of which require further investigation.     

SOIL CO2 FLUX IN GRASSLAND,AFFORESTED LAND AND RECLAIMED COALMINE OVERBURDEN DUMPS: A CASE STUDY

The aim of this study was to measure the in situ soil CO₂ flux from grassland, afforested land and reclaimed coalmine overburden dumps by using the automated soil CO₂ flux system (LICOR‐8100® infrared gas analyzer, LICOR Inc., Lincoln, NE). The highest soil CO₂ flux was observed in natural grassland (11·16 µmol CO₂ m⁻²s⁻¹), whereas the flux was reduced by 38 and 59 per cent in mowed site and at 15‐cm depth, respectively. The flux from afforested area was found 5·70 µmol CO₂ m⁻²s⁻¹, which is 50 per cent lower than natural grassland. In the reclaimed coalmine overburden dumps, the average flux under tree plantation was found to be lowest in winter and summer (0·89–1·12 µmol CO₂ m⁻²s⁻¹) and highest during late monsoon (3–3·5 µmol CO₂ m⁻²s⁻¹). During late monsoon, the moisture content was found to be higher (6–7·5 per cent), which leads to higher microbial activity and decomposition. In the same area under grass cover, soil CO₂ flux was found to be higher (8·94 µmol CO₂ m⁻²s⁻¹) compared with tree plantation areas because of higher root respiration and microbial activity. The rate of CO₂ flux was found to be determined predominantly by soil moisture and soil temperature. Our study indicates that the forest ecosystem plays a crucial role in combating global warming than grassland; however, to reduce CO₂ flux from grassland, mowing is necessary. Copyright © 2012 John Wiley & Sons, Ltd.