The Origin of Soil Organic C,Dissolved Organic C and Respiration in a Long‐Term Maize Experiment in Halle,Germany, Determined by 13C Natural Abundance

For a quantitative analysis of SOC dynamics it is necessary to trace the origins of the soil organic compounds and the pathways of their transformations. We used the ¹³C isotope to determine the incorporation of maize residues into the soil organic carbon (SOC), to trace the origin of the dissolved organic carbon (DOC), and to quantify the fraction of the maize C in the soil respiration. The maize‐derived SOC was quantified in soil samples collected to a depth of 65 cm from two plots, one ’︁continuous maize’ and the other ’︁continuous rye’ (reference site) from the long‐term field experiment ’︁Ewiger Roggen’ in Halle. This field trial was established in 1878 and was partly changed to a continuous maize cropping system in 1961. Production rates and δ¹³C of DOC and CO₂ were determined for the Ap horizon in incubation experiments with undisturbed soil columns. After 37 years of continuous maize cropping, 15% of the total SOC in the topsoil originated from maize C. The fraction of the maize‐derived C below the ploughed horizon was only 5 to 3%. The total amount of maize C stored in the profile was 9080 kg ha⁻¹ which was equal to about 31% of the estimated total C input via maize residues (roots and stubble). Total leaching of DOC during the incubation period of 16 weeks was 1.1 g m⁻² and one third of the DOC derived from maize C. The specific DOC production rate from the maize‐derived SOC was 2.5 times higher than that from the older humus formed by C₃ plants. The total CO₂‐C emission for 16 weeks was 18 g m⁻². Fifty‐eight percent of the soil respiration originated from maize C. The specific CO₂ formation from maize‐derived SOC was 8 times higher than that from the older SOC formed by C₃ plants. The ratio of DOC production to CO₂‐C production was three times smaller for the young, maize‐derived SOC than for the older humus formed by C₃ plants.     

Leaching of carbon and nitrogen from a sandy soil substrate: A comparison between suction plates and ion exchange resins

To determine boundary effects on leaching, we investigated (1) how filter materials affect the concentrations of dissolved organic carbon (DOC) and nitrate (NO₃‐N) in soil percolates and (2) whether ion exchange resins and suction plates are equally suited to capture NO₃‐N. DOC leaching was higher with PE suction plates and plate material did not affect NO₃‐N leachate concentrations. Cumulative NO₃‐N leaching was similar for glass suction plates and ion exchange resins.     

Long-term N addition effects on the C mineralization and DOC production in mor humus under spruce

This study was based on laboratory incubations of mor humus from two N fertilized stands of Norway spruce in Sweden (Skogaby and Stråsan), which had received repeated N additions (100 kg N ha⁻¹ yr⁻¹ as (NH₄)₂SO₄ at Skogaby and 35, 73 and 108 kg ha⁻¹ yr⁻¹ as NH₄NO₃ at Stråsan) during 8 and 24-29 years, respectively. The aim was to investigate long-term N effects on the mineralization of C and production of DOC. Mor humus (Oe and Oa) was incubated in columns at 20 °C for 49 days. Columns were leached once a week with artificial throughfall solution, which was analyzed for DOC, total N, NH₄⁺-N and NO₃⁻-N. Prior to each leaching event, CO₂ evolution from the columns was determined. C-to-N ratios in the N-treated Oe layers at Stråsan (21-24) and Skogaby (24) were significantly lower than those of the controls (Stråsan, 32; Skogaby, 28). The cumulative amount of CO₂-C showed a significant treatment effect in the Oe layer at Skogaby, i.e. 18 and 29 mg C g⁻¹ C in the N treatment and control, respectively. At Stråsan, the cumulative CO₂-C was significantly lower in the N3 treatment compared to the control in both layers (33 compared to 74 mg C g⁻¹ C in the Oe layer and 16 compared to 35 mg C g⁻¹ C in the Oa layer). Neither the DOC nor the DON production showed any significant treatment effects at the two sites. However, DOC was lower in the fertilized Oe layer at Skogaby throughout the incubation. The leaching of DON was highest in the Oe layers at both sites, and DON increased with time at Skogaby while there was a decreasing trend at Stråsan. The DOC-to-DON ratio tended to be lower in the fertilized Oe layers at both sites. The NH₄⁺ leaching at Skogaby decreased in the N-treated Oe and Oa layers. At Stråsan, NH₄⁺ from the Oe layer increased in N2 and control. The NO₃⁻ leaching was low and constant in both Skogaby layers. At Stråsan, NO₃⁻ increased in the Oe layer of N1. Cumulative CO₂ was positively correlated to C-to-N ratio (r2=0.71,p<0.01) and to cumulative DOC (r2=0.63,p<0.05) in the Oe layer at Stråsan. Our conclusion was that long-term N additions caused decreased C-to-N ratios and decreased CO₂ evolution rates. The correlation between CO₂ and C-to-N ratio in the Oe layers at Stråsan may be due to a changed quality of the fertilized forest floor material and presence of more N efficient microorganisms.     

Effect of temperature on the mineralization of C and N of fresh and mature compost in sandy material

Information about the mineralization rate of compost at various temperatures is a precondition to optimize mineral N fertilization and to minimize N losses in compost‐amended soils. Objectives were to quantify the influence of the temperature on the mineralization rate and leaching of dissolved organic carbon (DOC) and nitrogen (DON), NO₃^—, and NH₄⁺ from a fresh (C : N = 15.4) and a mature (C : N = 9.2) organic household waste compost. Compost samples were mixed with quartz sand to ensure aerobic conditions, incubated at 5, 10, 15, 20, and 25°C and irrigated weekly for 112 days. For the fresh compost, cumulative CO₂ evolution after 112 days ranged from 36% of the initial C content at 5°C to 54% at 25°C. The CO₂ evolution was only small in the experiments with mature compost (1 to 6% of the initial C content). The data were described satisfactorily by a combined first‐order (fresh compost) or a first‐order kinetic model (mature compost). For the fresh compost, cumulative DOC production was negatively related to the temperature, probably due to leaching of some of the partly metabolized easily degradable fractions at lower temperatures. The production ratios of DOC : CO₂‐C decreased with increasing temperature from 0.094 at 5°C to 0.038 at 25°C for the fresh and from 1.55 at 5°C to 0.26 at 25°C for the mature compost. In the experiments with fresh compost, net release of NO₃^— occurred after a time lag which depended on the temperature. Cumulative net release of NO₃^— after 112 days ranged from 1.8% of the initial N content at 5°C to 14.3% at 25°C. Approximately 10% of the initial N content of the mature compost was released as NO₃^— after 14 days at all temperatures. The DOC : DON ratios in the experiments using fresh compost ranged from 11.5 to 15.7 and no temperature dependency was observed. For the mature compost, DOC : DON ratios were slightly smaller (7.4 to 8.9). The DON : (NH₄⁺ + NO₃^—) ratio decreased with increasing temperature from 0.91 at 5°C to 0.19 at 25°C for the fresh compost and from 0.21 at 5°C to 0.12 at 25°C for the mature compost. The results of the dynamics of C and N mineralization of fresh and mature compost can be used to assess the appropriate application (timing and amount) of compost to soils.     

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.     

Different effect of drying on the fluxes of dissolved organic carbon and nitrogen from a Norway spruce forest floor

The forest floor represents the major source of dissolved organic carbon (DOC) and nitrogen (DON) in forest soils. The release mechanisms of DOC and DON from forest floors and their environmental controls as well as the dynamics of concentrations and fluxes are still poorly understood. We investigated the effect of drying and rewetting on the release of DOC and DON from a Norway spruce forest floor. Undisturbed soil columns of 17 cm diameter and 15—20 cm height were taken with 7 replicates from the forest floor of a mature Norway spruce (Picea abies [L.] Karst.) site and established at 10°C in the laboratory. Columns were exposed to different periods of drying (3, 5, 10, 20 days). Each drying period was followed by a rewetting for 5 days at an irrigation rate of 10 mm d^—1 with a natural throughfall solution. The percolates from the forest floor were collected daily and analyzed for DOC, total N, NH₄, NO₃, pH, electrical conductivity and major ions. Drying for 10 and 20 days decreased the water content of the Oi horizon from 280% dry weight to about 30%. The water content of the Oe and the Oa horizon only changed from about 300% to 200%. The fluxes of DOC from the forest floor were moderately effected by drying and rewetting with an increase after 3 and 5 days of drying, but a decrease after 10 and 20 days. On the contrary, the drying for 10 and 20 days resulted in a drastic increase of the DON fluxes and a subsequent decrease of the DOC/DON ratios in the forest floor percolates from about 50 to 3.3. These results suggest that the mechanisms for DOC release in forest floors differ from those for DON and that drying and rewetting cause temporal variations in the DOC/DON ratios in forest floor percolates.     

Plant roots are more important than temperature in modulating carbon release in a limed acidic soil

Lime is a common amendment to overcome soil acidity in agricultural production systems. However, plant root effects on lime and soil carbon (C) dynamics in acidic soils under varied temperature remain largely unknown. We monitored root effects of soybean on the fate of lime applied to an acidic soil at 20 and 30°C in growth chambers. Soil respired CO₂ was continuously trapped in columns without and with plants until the final stage of vegetative growth. Lime‐derived CO₂ was separated from total respired CO₂ based on δ¹³C measurements in CO₂. Leaching was induced at early and late vegetative growth stages, and the leachates were analysed for dissolved organic (DOC) and inorganic C (DIC) concentrations. Soil respiration significantly increased with lime addition at both temperatures (p < 0.001). The presence of soybean doubled the recovery of lime‐derived CO₂‐C at 20°C at the early growth stage; however, by the end of the experiment, the contribution of lime‐derived CO₂‐C to soil respiration was negligible in all treatments, indicating that the contribution of lime to soil respiration was shortlived. In contrast, DIC and DOC concentrations in leachates remained elevated with liming and were greater in the presence of soybean. We observed no main temperature effects and no interactive effects of temperature and soybean presence on lime‐derived CO₂‐C, DIC and DOC. These results highlight the role of plant‐modulated processes in CO₂ release and C leaching from lime in acidic soils, whereas an increase in temperature may be less important. Temperature and plant roots alter the rate of key processes controlling C dynamics in a limed acidic soil. Lime‐derived CO₂‐C, DIC and DOC increased more in the presence of plants than with increased temperature. Root effects are more important than temperature for inorganic and organic carbon dynamics in limed acidic soils.     

Carbon dynamics determined by natural C abundance in microcosm experiments with soils from long-term maize and rye monocultures

Understanding carbon dynamics in soil is the key to managing soil organic matter. Our objective was to quantify the carbon dynamics in microcosm experiments with soils from long-term rye and maize monocultures using natural ¹³C abundance. Microcosms with undisturbed soil columns from the surface soil (0-25 cm) and subsoil (25-50 cm) of plots cultivated with rye (C₃-plant) since 1878 and maize (C₄-plant) since 1961 with and without NPK fertilization from the long-term experiment ‘Ewiger Roggen’ in Halle, Germany, were incubated for 230 days at 8 °C and irrigated with 2 mm 10⁻² M CaCl₂ per day. Younger, C₄-derived and older, C₃-derived percentages of soil organic carbon (SOC), dissolved organic carbon (DOC), microbial biomass (C_mic) and CO₂ from heterothropic respiration were determined by natural ¹³C abundance. The percentage of maize-derived carbon was highest in CO₂ (42-79%), followed by C_mic (23-46%), DOC (5-30%) and SOC (5-14%) in the surface soils and subsoils of the maize plots. The percentage of maize-derived C was higher for the NPK plot than for the unfertilized plot and higher for the surface soils than for the subsoils. Specific production rates of DOC, CO₂-C and C_mic from the maize-derived SOC were 0.06-0.08% for DOC, 1.6-2.6% for CO₂-C and 1.9-2.7% for C_mic, respectively, and specific production rates from rye-derived SOC of the continuous maize plot were 0.03-0.05% for DOC, 0.1-0.2% for CO₂-C and 0.3-0.5% for C_mic. NPK fertilization did not affect the specific production rates. Strong correlations were found between C₄-derived C_mic and C₄-derived SOC, DOC and CO₂-C (r≥0.90), whereas the relationship between C₃-derived C_mic and C₃-derived SOC, DOC and CO₂-C was not as pronounced (r≤0.67). The results stress the different importance of former (older than 40 years) and recent (younger than 40 years) litter C inputs for the formation of different C pools in the soil.     

Denitrification Rate and Controlling Factors for Accumulated Nitrate in the Deep Subsoil of Intensive Farmlands: A Case Study in the North China Plain

Denitrification in subsoil(to a depth of 12 m) is an important mechanism to reduce nitrate(NO_3~-) leaching into groundwater.However, regulating mechanisms of subsoil denitrification, especially those in the deep subsoil beneath the crop root zone, have not been well documented. In this study, soil columns of 0–12 m depth were collected from intensively farmed fields in the North China Plain. The fields had received long-term nitrogen(N) fertilizer inputs at 0(N0), 200(N200) and 600(N600) kg N ha~(-1) year~(-1). Main soil properties related to denitrification, i.e., soil water content, NO_3~-, dissolved organic carbon(DOC), soil organic carbon(SOC),pH, denitrifying enzyme activity(DEA), and anaerobic denitrification rate(ADR), were determined. Statistical comparisons among the treatments were performed. The results showed that NO_3~- was more heavily accumulated in the entire soil profile of the N600 treatment, compared to the N0 and N200 treatments. The SOC, DOC, and ADR decreased with increasing soil depth in all treatments,whereas considerable DEA was observed throughout the subsoil. The long-term fertilizer rates affected ADR only in the upper 4 m soil layers. The ADRs in the N200 and N600 treatments were significantly correlated with DOC. Multiple regression analysis indicated that DOC rather than DEA was the key factor regulating denitrification beneath the root zone. Additional research is required to determine if carbon addition into subsoil can be a promising approach to enhance NO_3~- denitrification in the subsoil and consequently to mitigate groundwater NO_3~- contamination in the intensive farmlands.     

Effects of rainfall pattern on carbon and nitrogen dynamics in soil amended with biogas slurry and composted cattle manure

Soil moisture affects the degradation of organic fertilizers in soils considerably, but less is known about the importance of rainfall pattern on the turnover of C and N. The objective of this study was to determine the effects of different rainfall patterns on C and N dynamics in soil amended with either biogas slurry (BS) or composted cattle manure (CM). Undisturbed soil cores without (control) or with BS or CM, which were incorporated at a rate of 100 kg N ha^–1, were incubated for 140 d at 13.5°C. Irrigation treatments were (1) continuous irrigation (cont_irr; 3 mm d^–1); (2) partial drying and stronger irrigation (part_dry; no irrigation for 3 weeks, 1 week with 13.5 mm d^–1), and (3) periodic heavy rainfall (hvy_rain; 24 mm d^–1 every 3 weeks for 1 d and 2 mm d^–1 for the other days). The average irrigation was 3 mm d^–1 in each treatment. Cumulative emissions of CO₂ and N₂O from soils amended with BS were 92.8 g CO₂‐C m^–2 and 162.4 mg N₂O‐N m^–2, respectively, whereas emissions from soils amended with CM were 87.8 g CO₂‐C m^–2 and only 38.9 mg N₂O‐N m^–2. While both organic fertilizers significantly increased CO₂ production compared to the control, N₂O emissions were only significantly increased in the BS‐amended soil. Under the conditions of the experiment, the rainfall pattern affected the temporal production of CO₂ and N₂O, but not the cumulative emissions. Cumulative NO leaching was highest in the BS‐amended soils (9.2 g NO ‐N m^–2) followed by the CM‐amended soil (6.1 g NO ‐N m^–2) and lowest in the control (4.7 g NO ‐N m^–2). Nitrate leaching was also independent of the rainfall pattern. Our study shows that rainfall pattern may not affect CO₂ and N₂O emissions and NO leaching markedly provided that the soil does not completely dry out.     

Retention of dissolved organic matter by illitic soils and clay fractions: Influence of mineral phase properties

The dependency of the retention of dissolved organic carbon (DOC) on mineral phase properties in soils remains uncertain especially at neutral pH. To specifically elucidate the role of mineral surfaces and pedogenic oxides for DOC retention at pH 7, we sorbed DOC to bulk soil (illitic surface soils of a toposequence) and corresponding clay fraction (< 2 μm) samples after the removal of organic matter and after removal of organic matter and pedogenic oxides. The DOC retention was related to the content of dithionite‐extractable iron, specific surface area (SSA, BET‐N₂ method) and cation exchange capacity (pH 7). The reversibility of DOC sorption was determined by a desorption experiment. All samples sorbed 20–40 % of the DOC added. The DOC sorption of the clay fractions explained the total sorption of the bulk soils. None of the mineral phase properties investigated was able to solely explain the DOC retention. A sorption of 9 to 24 μg DOC m^–2 indicated that DOC interacted only with a fraction of the mineral surface, since loadings above 500 μg m^–2 would be expected for a carbon monolayer. Under the experimental conditions used, the surface of the silicate clay minerals seemed to be more important for the DOC sorption than the surface of the iron oxides. The desorption experiment removed 11 to 31 % of the DOC sorbed. Most of the DOC was strongly sorbed.     

Nitrous oxide emissions as influenced by amendment of plant residues with different C:N ratios

To investigate the influence of plant residues decomposition on N₂O emission, laboratory incubations were carried out for a period of 21 days using urea and five plant residues with a wide range of C:N ratios from 8 to 118. Incorporation of plant residues enhanced N₂O and CO₂ emissions. The two gas fluxes were significantly correlated (R²=0.775, p<0.001). Cumulative emissions of N₂O and CO₂ were negatively correlated with the C:N ratio in plant residues (R²=0.783 and 0.986 for N₂O, and 0.854 for CO₂, respectively). A negative relationship between the N₂O-N/NO₃⁻-N ratio and the C:N ratio was observed (R²=0.867) when residue plus urea was added. We calculated the changes in dissolved organic C (DOC) and the relevant changes in N₂O emission. The incorporation of residues increased DOC when compared with the control, while the incorporation of residue plus urea decreased DOC. Cumulative emissions of N₂O and CO₂ were positively correlated with DOC concentration measured at the end of the incubation. In addition, the N₂O emission fraction, defined as N₂O-N emissions per unit N input, was not found to be a constant for either residue-N or urea-N amendment but dependent on C:N ratio when plant residue was incorporated.     

Microbial decomposition of leached or extracted dissolved organic carbon and nitrogen from pasture soils

Microbial decomposition of extracted and leached dissolved organic carbon (DOC) and nitrogen (DON) was demonstrated from three pasture soils in laboratory incubation studies. DOC concentration in water extracts ranged between 29 and 148 mg C L^?1 and DON concentration ranged between 2 and 63 mg N L^?1. Between 17 and 61 % of the DOC in the water extracts were respired as CO₂ by microbes by day 36. DON concentrations in the extracts declined more rapidly than DOC. Within the first 21 days of incubation, the concentration of DON was near zero without any significant change in the concentration of NO₃ ^? or NH₄ ⁺, indicating that microbes had utilized the organic pool of N preferentially. Decomposition of leached DOC (ranged between 7 and 66 mg C L^?1) and DON (ranged between 6 and 11 mg N L^?1) collected from large lysimeters (with perennial pasture; 50 cm diameter?×?80 cm deep) followed a similar pattern to that observed with soil extracts. Approximately 28 to 61 % of the DOC in leachates were respired as CO₂ by day 49. The concentration of DON in the leachates declined to below 1 mg N L^?1 within 7–14 days of the incubation, consistent with the observations made with extractable DON. Our results clearly show that DOC and DON components of the dissolved organic matter in pasture soils, whether extracted or leached, are highly decomposable and bioavailable and will influence local ecosystem functions and nutrient balances in grazed pasture systems and receiving water bodies.     

Fate of Chinese-fir litter during decomposition as a result of inorganic N additions

We conducted a controlled experiment to evaluate Chinese-fir litter decomposition and its response to the addition of inorganic N. Litter-derived CO₂, microbial biomass carbon (MBC), and dissolved organic carbon (DOC) were monitored during an 87-d incubation of a mixed soil–litter substrate using the ¹³C tracer technique. Litter C was mostly converted to CO₂ (47.4% of original mass), followed by MBC (3.6%), and DOC (1.0%), with 48% remaining unaltered in the soil. The litter decomposition rate significantly increased with the addition of inorganic N, although the effect depended on whether N was added as NH₄⁺ or NO₃⁻. Soil-derived CO₂, MBC, and DOC also increased following the combined addition of litter and N. The results showed that only a small percentage of litter C was retained as MBC or DOC and that the conversion rate depended, in part, on the form of inorganic N added to the Chinese-fir plantation soil.     

Aeration effects on CO2, N2O,and CH4 emission and leachate composition of a forest soil

The availability of O₂ is one of the most important factors controlling the chemical and biological reactions in soils. In this study, the effects of different aeration conditions on the dynamics of the emission of trace gases (CO₂, N₂O, CH₄) and the leachate composition (NO₃^‐, DOC, Mn, Fe) were determined. The experiment was conducted with naturally structured soil columns (silty clay, Vertisol) from a well aerated forest site. The soil monoliths were incubated in a microcosm system at different O₂ concentrations (0, 0.001, 0.005, 0.01, 0.05, and 0.205 m³ m^‐3 in the air flow through the headspace of the microcosms) for 85 days. Reduced O₂ availability resulted in a decreased CO₂ release but in increased N₂O emission rates. The greatest cumulative N₂O emissions (= 1.6 g N₂O‐N m^‐2) were observed at intermediate O₂ concentrations (0.005 and 0.01 m³ m^‐3) when both nitrification and denitrification occurred simultaneously in the soil. Cumulative N₂O emissions were smallest (= 0.05 g N₂O‐N m^‐2) for the aeration with ambient air (O₂ concentration: 0.205 m³ m^‐3), although nitrate availability was greatest in this treatment. The emission of CH₄ and leaching of Mn and Fe were restricted to the soil columns incubated under completely anoxic conditions. The sequence of the reduction processes under completely anoxic conditions complied with the thermodynamic theory: soil nitrate was reduced first, followed by the reduction of Mn(IV) and Fe(III) and finally CO₂ was reduced to CH₄. The re‐aeration of the soil columns after 85 days of anoxic incubation terminated the production of CH₄ and dissolved Fe and Mn in the soil but strongly increased the emission rates of CO₂ and N₂O and the leaching of NO₃^‐ probably because of the accumulation of DOC and NH₄⁺ during the previous anoxic period.     

Application of the end-of-season stalk nitrate test for a high-yield maize production system in Northwestern China

Excessive nitrogen application has caused serious environmental pollution under high-yield maize system in China. Our objective was to evaluate critical stalk nitrate (NO₃^?) levels that support high yield (>13 Mgha^?1), but are not in excess. Optimal stalk NO₃^? concentration was determined by conducting seven nitrogen levels experiments in two high yield maize regions: Dongyang County (DY) and Wenshui County (WS). Optimal stalk NO₃^? concentration category range to obtain maximum yield in DY (sandy loam, higher accumulated temperature and solar radiation compared with WS) was 0.44–1.19, which similar to the criteria of US (0.70–2.0 g kg^?1). While for WS (loam soil, lower accumulated temperature and solar radiation compared with DY), optimal stalk NO₃^? concentration category range to obtain maximum yield was 1.95–4.15, greatly higher than the US criteria. These results suggested thatit is necessary to establish matching optimal stalk NO₃^? category ranges for different ecological regions in China.     

Repeated freeze–thaw events affect leaching losses of nitrogen and dissolved organic matter in a forest soil

Freezing and thawing may substantially influence the rates of C and N cycling in soils, and soil frost was proposed to induce NO losses with seepage from forest ecosystems. Here, we test the hypothesis that freezing and thawing triggers N and dissolved organic matter (DOM) release from a forest soil after thawing and that low freezing temperatures enhance the effect. Undisturbed soil columns were taken from a soil at a Norway spruce site either comprising only O horizons or O horizons + mineral soil horizons. The columns were subjected to three cycles of freezing and thawing at temperatures of –3°C, –8°C, and –13°C. The control columns were kept at constant +5°C. Following the frost events, the columns were irrigated for 20 d at a rate of 4 mm d^–1. Percolates were analyzed for total N, mineral N, and dissolved organic carbon (DOC). The total amount of mineral N extracted from the O horizons in the control amounted to 8.6 g N m^–2 during the experimental period of 170 d. Frost reduced the amount of mineral N leached from the soil columns with –8°C and –13°C being most effective. In these treatments, only 3.1 and 4.0 g N m^–2 were extracted from the O horizons. Net nitrification was more negatively affected than net ammonification. Severe soil frost increased the release of DOC from the O horizons, but the effect was only observed in the first freeze–thaw cycle. We found no evidence for lysis of microorganisms after soil frost. Our experiment did not confirm the hypothesis that soil frost increases N mineralization after thawing. The total amount of additionally released DOC was rather low in relation to the expected annual fluxes.     

Natural 13C abundance and soil carbon dynamics under long‐term residue retention in a no‐till maize system

Residue retention and reduced tillage are both conservation agricultural practices that may enhance soil organic carbon (SOC) stabilization in soil. We evaluated the long‐term effects of no‐till (NT) and stover retention from maize on SOC dynamics in a Rayne silt loam Typic Hapludults in Ohio. The six treatments consisted of retaining 0, 25, 50, 75, 100 and 200% of maize residues on each 3 × 3 m plot from the crop of previous year. Soil samples were obtained after 9 yrs of establishing the experiment. The whole soil (0–10 and 10–20 cm of soil depths) samples under different treatments were analysed for total C, total N, recalcitrant C (NaOCl treated sample) and ¹³C isotopic abundance (0–10 cm soil depth). Complete removal of stover for a period of 9 yrs significantly (P < 0.01) decreased soil C content (15.5 g/kg), whereas 200% of stover retention had the maximum soil C concentration (23.1 g/kg). Relative distribution of C for all the treatments in different fractions comprised of 55–58% as labile and 42–45% as recalcitrant. Retention of residue did not significantly affect total C and N concentration in 10–20 cm depth. ¹³C isotopic signature data indicated that C₄‐C (maize‐derived C) was the dominant fraction of C in the top 0–10 cm of soil layer under NT with maize‐derived C accounting for as high as 80% of the total SOC concentration. Contribution of C₄‐C or maize‐derived C was 71–84% in recalcitrant fraction in different residue retained plots. Residue management is imperative to increase SOC concentrations and long‐term agro‐ecosystem necessitates residue retention for stabilizing C in light‐textured soils.     

Rhizodeposition of maize: Short‐term carbon budget and composition

The aim of this study was to assess differences in rhizodeposition quantity and composition from maize cropped on soil or on 1:1 (w/w) soil–sand mixture and distribution of recently assimilated C between roots, shoots, soil, soil solution, and CO₂ from root respiration. Maize was labeled in ¹⁴CO₂ atmosphere followed by subsequent simultaneous leaching and air flushing from soil. ¹⁴C was traced after 7.5 h in roots and shoots, soil, soil solution, and soil‐borne CO₂. Rhizodeposits in the leachate of the first 2 h after labeling were identified by high‐pressure liquid chromatography (HPLC) and pyrolysis–field ionization mass spectrometry (Py‐FIMS). Leachate from soil–sand contained more ¹⁴C than from soil (0.6% vs. 0.4%) and more HPLC‐detectable carboxylates (4.36 vs. 2.69 μM), especially acetate and lactate. This is either because of root response to lower nutrient concentrations in the soil–sand mixture or decreasing structural integrity of the root cells during the leaching process, or because carboxylates were more strongly sorbed to the soil compared to carbohydrates and amino acids. In contrast, Py‐FIMS total ion intensity was more than 2 times higher in leachate from soil than from soil–sand, mainly due to signals from lignin monomers. HPLC‐measured concentrations of total amino acids (1.33 μM [soil] vs. 1.03 μM [soil–sand]) and total carbohydrates (0.73 vs. 0.34 μM) and ¹⁴CO₂ from soil agreed with this pattern. Higher leachate concentrations from soil than from soil–sand for HPLC‐measured carbohydrates and amino acids and for the sum of substances detected by Py‐FIMS overcompensated the higher sorption in soil than in sand‐soil. A parallel treatment with blow‐out of the soil air but without leaching indicated that nearly all of the rhizodeposits in the treatment with leaching face decomposition to CO₂. Simultaneous application of three methods—¹⁴C‐labeling and tracing, HPLC, and Py‐FIMS—enabled us to present the budget of rhizodeposition (¹⁴C) and to analyze individual carbohydrates, carboxylates, and amino acids (HPLC) and to scan all dissolved organic substances in soil solution (Py‐FIMS) as dependent on nutrient status.     

Short-term effects of an exceptionally hot and dry summer on decomposition of surface peat in a restored temperate bog

The restoration of drained peat bogs in Northwest (NW) Europe is an important task of soil protection, but needs to cope with warmer and drier summers. Our examination took place in the Pietzmoor bog (Schneverdingen, NW Germany) that had been drained for fuel peat extraction until the 1970s and rewetted since then. We determined carbon dioxide (CO₂) efflux in situ and in laboratory incubations. Also, we analyzed pore water for dissolved organic carbon (DOC), total and dissolved organic N (DON), nitrate (NO₃^–) and ammonium (NH₄⁺) concentration. In Schneverdingen, the summer 2003 was record-breaking hot (mean temperature June to August elevated > 3 K compared to long-term average) and dry (precipitation during the same period < 59% of long-term average). In July 2003, the water table in the Pietzmoor subsided to > 42 cm below the surface in July 2003, when in situ soil CO₂ efflux was up to 23.4 g m^–2 d^–1 compared to 15.7 g m^–2 d^–1 in September. Prior to March 2003, DOC concentrations in pore water were < 180 mg l^–1 and NH₄⁺ was the dominant fraction of mineral N. In July 2003, DOC concentration rose to 249 g l^–1, DON concentrations more than doubled, and NO₃^– became the dominant fraction of mineral N. Due to the increased future likelihood of hot and dry summers in NW Germany, peat bog restoration efforts need take care that a water table close to the surface is maintained.