Temperature sensitivity of soil organic matter decomposition varies with biochar application and soil type

Biochar application has the potential to improve soil fertility and increase soil carbon stock, especially in tropical regions. Information on the temperature sensitivity of carbon dioxide(CO_2) evolution from biochar-amended soils at very high temperatures, as observed for tropical surface soils, is limited but urgently needed for the development of region-specific biochar management targeted to optimize biochar effects on soil functions. Here, we investigated the temperature sensitivity of soil respiration to the addition of different rates of Miscanthus biochar(0, 6.25, 12.5, and 25 Mg ha~(-1)) in two types of soils with contrasting textures. Biochar-amended soil treatments and their controls were incubated at constant temperatures of 20, 30, and 40℃. Overall, our results show that: i) considering data from all treatments and temperatures, the addition of biochar decreased soil CO_2 emissions when compared to untreated soils;ii) CO_2 emissions from biochar-amended soils had a higher temperature sensitivity than those from biochar-free soils; iii) the temperature sensitivity of soil respiration in sandy soils was higher than that in clay soils; and iv) for clay soils, relative increases in soil CO_2 emissions from biochar-amended soils were higher when the temperature increased from 30 to 40℃, while for sandy soils, the highest temperature responses of soil respiration were observed when increasing the temperature from 20 to 30℃. Together, these findings suggest a significantly reduced potential to increase soil organic carbon stocks when Miscanthus biochar is applied to tropical soils at high surface temperatures, which could be counteracted by the soil-and weather-specific timing of biochar application.     

Formation of carcinogenic nitrosamines in soils

The possible formation of carcinogenic nitrosamines in soils was examined. Soil samples amended with NO₂^?-N and dimethylamine incubated for 30 days and analysed every 3 days, showed increasing amounts of dimethylnitrosamine up to 12–15 days. The concentration reached as high as 6.5 parts/10⁶, thereafter, a decline was noted. Most of the nitrosamines disappeared in soils after 30 days. Addition of inorganic N reduced the decomposition of dimethylamine. Soil incubation studies with NO₂^? and trimethylamine showed about 80% reduction in the amount of nitrosamines formed as compared to dimethylamine. Analysis of soil samples from fertilized and polluted areas showed significant amounts of NO^?₃-N but no nitrosamines. Application of 10 parts/10⁶ of dimethylamine to these soil samples resulted in the formation of 0.10 to 0.50 parts/10⁶ of nitrosamines. Autoclaved soil samples incubated with NO₂^? and dimethylamine for 12–15 days produced small amounts of nitrosamines. Addition of glucose to soil samples increased the amounts of nitrosamines formed.     

No-till only increases N2O emissions in poorly-aerated soils

Denitrification rates are often greater in no-till than in tilled soils and net soil-surface greenhouse gas emissions could be increased by enhanced soil N₂O emissions following adoption of no-till. The objective of this study was to summarize published experimental results to assess whether the response of soil N₂O fluxes to the adoption of no-till is influenced by soil aeration. A total of 25 field studies presenting direct comparisons between conventional tillage and no-till (approximately 45 site-years of data) were reviewed and grouped according to soil aeration status estimated using drainage class and precipitation during the growing season. The summary showed that no-till generally increased N₂O emissions in poorly-aerated soils but was neutral in soils with good and medium aeration. On average, soil N₂O emissions under no-till were 0.06 kg N ha⁻¹ lower, 0.12 kg N ha⁻¹ higher and 2.00 kg N ha⁻¹ higher than under tilled soils with good, medium and poor aeration, respectively. Our results therefore suggest that the impact of no-till on N₂O emissions is small in well-aerated soils but most often positive in soils where aeration is reduced by conditions or properties restricting drainage. Considering typical soil C gains following adoption of no-till, we conclude that increased N₂O losses may result in a negative greenhouse gas balance for many poorly-drained fine-textured agricultural soils under no-till located in regions with a humid climate.     

Long-term large N and immediate small N addition effects on trace gas fluxes in the Colorado shortgrass steppe

 Land use changes in semiarid grasslands have long-lasting effects. Reversion to near-original conditions with respect to plant populations and productivity requires more than 50 years following plowing. The impact of more subtle management changes like small, annual applications of N fertilizer or changing cattle stocking rates, which alters N redistribution caused by grazing and cattle urine deposition, is not known. To investigate the long-term effects of N addition to the Colorado shortgrass steppe we made weekly, year-round measurements of N₂O and CH₄ from the spring of 1990 through June 1996. Fluxes of NO_x (NO plus NO₂) were measured from October 1995 through June 1996. These measurements illustrated that large N applications, either in a single dose (45 g N m^–2), simulating cattle urine deposition, or in small annual applications over a 15-year period (30 g N m^–2) continued to stimulate N₂O emissions from both sandy loam and clay loam soils 6–15 years after N application. In sandy loam soils last fertilized 6 years earlier, average NO_x emissions were 60% greater than those from a comparable, unfertilized site. The long-term impact of these N additions on CH₄ uptake was soil-dependent, with CH₄ uptake decreased by N addition only in the coarser textured soils. The short-term impact of small N additions (0.5–2 g N m^–2) on N₂O, NO_x emissions and CH₄ uptake was observed in field studies made during the summer of 1996. There was little short-term effect of N addition on CH₄ uptake in either sandy loam or clay loam soils. Small N additions did not result in an immediate increase in N₂O emissions from the sandy loam soil, but did significantly increase N₂O flux from the clay loam soil. The reverse soil type, N addition interaction occurred for NO_x emissions where N addition increased NO_x emissions in the coarser textured soil 10–20 times those of N₂O. Received: 31 October 1997     

Soil engineering ants increase CO2 and N2O emissions by affecting mound soil physicochemical characteristics from a marsh soil: A laboratory study

As ecosystem engineers, ants can mediate soil processes and functions by producing biogenic structures. In their mounds, ants not only directly produce CO₂ by respiration, but may also indirectly impact soil greenhouse gas emissions by affecting substrate availability and soil physicochemical characteristics. Recent studies focused on overall gas production from ant mounds. However, little is known about mound material respiration and N₂O emissions in ant mounds in wetlands. We measured CO₂ and N₂O emissions from mound soils of three different ant species (Lasius niger Linnaeus, Lasius flavus Fabricius, and Formica candida Smith) and natural marsh soils in a laboratory incubation experiment. On the whole, average soil CO₂ and N₂O emission rates from ant mounds were significantly higher than from the natural marsh soils. Over the 64 days incubation, the cumulative soil CO₂ and N₂O production from ant mounds was, respectively, 1.5–3.0 and 1.9–50.2 times higher than from the natural soils. Soil gas emissions from ant mounds were significantly influenced by the specific ant species, with soil CO₂ and N₂O emissions from L. niger mounds being higher than those from F. candida or L. flavus mound soils. Cumulative CO₂ and N₂O emissions from ant mound soils were positively correlated with soil clay, total carbon, dissolved organic carbon, total nitrogen and NH₄⁺ content. Our laboratory results indicated that mound soil is an important source of CO₂ and N₂O emission from ant mounds in marshes, making mounds potential “hot spots” for CO₂ and N₂O emissions. Ants may increase the spatial heterogeneity of soil gas emissions by changing mound soil physicochemical properties, especially carbon and nutrition content, and soil texture. Contributions from ant mound materials should be considered when describing soil C and N cycles and their driving factors in wetland ecosystems.     

Variability of CO2 and N2O emissions during freeze‐thaw cycles: results of model experiments on undisturbed forest‐soil cores

The amounts of N₂O released in periods of alternate freezing and thawing depend on site and freezing conditions, and contribute considerably to the annual N₂O emissions. However, quantitative information on the N₂O emission level of forest soils in freeze‐thaw cycles is scarce, especially with regard to the direct and indirect effect of tree species and the duration of freezing. Our objectives were (i) to quantify the CO₂ and N₂O emissions of three soils under beech which differed in their texture, C and N contents, and humus types in freeze‐thaw cycles, and (ii) to study the effects of the tree species (beech (Fagus sylvatica L.) and spruce (Picea abies (L.) Karst.)) for silty soils from two adjacent sites and the duration of freezing (three and eleven days) on the emissions. Soils were adjusted to a matric potential of –0.5 kPa, and emissions were measured in 3‐hr intervals for 33 days. CO₂ emissions of all soils were similar in the two freeze‐thaw cycles, and followed the temperature course. In contrast, the N₂O emissions during thawing differed considerably. Large N₂O emissions were found on the loamy soil under beech (Loam‐beech) with a maximum N₂O emission of 1200 μg N m^–2 h^–1 and a cumulative emission of 0.15 g N m^–2 in the two thawing periods. However, the sandy soil under beech (Sand‐beech) emitted only 1 mg N₂O‐N m^–2 in the two thawing periods probably because of a low water‐filled pore space of 44 %. The N₂O emissions of the silty soil under beech (Silt‐beech) were small (9 mg N m^–2 in the two thawing periods) with a maximum emission of 150 μg N m^–2 h^–1 while insignificant N₂O emissions were found on the silty soil under spruce (0.2 mg N m^–2 in the two thawing periods). The cumulative N₂O emissions of the short freeze‐thaw cycles were 17 % (Sand‐beech) or 22 % (Loam‐beech, Silt‐beech) less than those of the long freeze‐thaw cycles, but the differences between the emissions of the two periods were not significant (P ≤ 0.05). The results of the study show that the amounts of N₂O emitted in freeze‐thaw cycles vary markedly among different forest soils and that the tree species influence the N₂O thawing emissions in forests considerably due to direct and indirect impacts on soil physical and chemical properties, soil structure, and properties of the humus layer.     

Functional dependencies of soil CO2 emissions on soil biological properties in northern German agricultural soils derived from a glacial till

Agricultural soil CO₂ emissions and their controlling factors have recently received increased attention because of the high potential of carbon sequestration and their importance in soil fertility. Several parameters of soil structure, chemistry, and microbiology were monitored along with soil CO₂ emissions in research conducted in soils derived from a glacial till. The investigation was carried out during the 2012 growing season in Northern Germany. Higher potentials of soil CO₂ emissions were found in grassland (20.40 µg g^?1 dry weight h^?1) compared to arable land (5.59 µg g^?1 dry weight h^?1) within the incubating temperature from 5°C to 40°C and incubating moisture from 30% to 70% water holding capacity (WHC) of soils taken during the growing season. For agricultural soils regardless of pasture and arable management, we suggested nine key factors that influence changes in soil CO₂ emissions including soil temperature, metabolic quotient, bulk density, WHC, percentage of silt, bacterial biomass, pH, soil organic carbon, and hot water soluble carbon (glucose equivalent) based on principal component analysis and hierarchical cluster analysis. Slightly different key factors were proposed concerning individual land use types, however, the most important factors for soil CO₂ emissions of agricultural soils in Northern Germany were proved to be metabolic quotient and soil temperature. Our results are valuable in providing key influencing factors for soil CO₂ emission changes in grassland and arable land with respect to soil respiration, physical status, nutrition supply, and microbe-related parameters.     

Impact of biochar addition to soil on greenhouse gas emissions following pig manure application

The application of biochar produced from wood and crop residues, such as sawdust, straw, sugar bagasse and rice hulls, to highly weathered soils under tropical conditions has been shown to influence soil greenhouse gas (GHG) emissions. However, there is a lack of data concerning GHG emissions from soils amended with biochar derived from manure, and from soils outside tropical and subtropical regions. The objective of this study was to quantify the effect on emissions of carbon dioxide (CO₂), nitrous oxide (N₂O) and methane (CH₄) following the addition, at a rate of 18 t ha⁻¹, of two different types of biochar to an Irish tillage soil. A soil column experiment was designed to compare three treatments (n = 8): (1) non-amended soil (2) soil mixed with biochar derived from the separated solid fraction of anaerobically digested pig manure and (3) soil mixed with biochar derived from Sitka Spruce (Picea sitchensis). The soil columns were incubated at 10 °C and 75% relative humidity, and leached with 80 mL distilled water, twice per week. Following 10 weeks of incubation, pig manure, equivalent to 170 kg nitrogen ha⁻¹ and 36 kg phosphorus ha⁻¹, was applied to half of the columns in each treatment (n = 4). Gaseous emissions were analysed for 28 days following manure application. Biochar addition to the soil increased N₂O emissions in the pig manure-amended column, most likely as a result of increased denitrification caused by higher water filled pore space and organic carbon (C) contents. Biochar addition to soil also increased CO₂ emissions. This was caused by increased rates of C mineralisation in these columns, either due to mineralisation of the labile C added with the biochar, or through increased mineralisation of the soil organic matter.     

N2O emissions from an irrigated and non‐irrigated organic soil in eastern Canada as influenced by N fertilizer addition

Drainage and cultivation of organic soils often result in large nitrous oxide (N₂O) emissions. The objective of this study was to assess the impacts of nitrogen (N) fertilizer on N₂O emissions from a cultivated organic soil located south of Montréal, QC, Canada, drained in 1930 and used since then for vegetable production. Fluxes of N₂O were measured weekly from May 2004 to November 2005 when snow cover was absent in irrigated and non‐irrigated plots receiving 0, 100 or 150 kg N ha⁻¹ as NH₄NO₃. Soil mineral N content, gas concentrations, temperature, water table height and water content were also measured to help explain variations in N₂O emissions. Annual emissions during the experiment were large, ranging from 3.6 to 40.2 kg N₂O‐N ha⁻¹ year⁻¹. The N₂O emissions were decreased by N fertilizer addition in the non‐irrigated site but not in the irrigated site. The absence of a positive influence of soil mineral N content on N₂O emissions was probably in part because up to 571 kg N ha⁻¹ were mineralized during the snow‐free season. Emissions of N₂O were positively correlated to soil CO₂ emissions and to variables associated with the extent of soil aeration such as soil oxygen concentration, precipitation and soil water table height, thereby indicating that soil moisture/aeration and carbon bioavailability were the main controls of N₂O emission. The large N₂O emissions observed in this study indicate that drained cultivated organic soils in eastern Canada have a potential for N₂O‐N losses similar to, or greater than, organic soils located in northern Europe.     

Efficiency of nitrification inhibitor DMPP to reduce nitrous oxide emissions under different temperature and moisture conditions

Agricultural intensification has led to the use of very high inputs of nitrogen fertilizers into cultivated land. As a consequence of this, nitrous oxide (N₂O) emissions have increased significantly. Nowadays, the challenge is to mitigate these emissions in order to reduce global warming. Addition of nitrification inhibitors (NI) to fertilizers can reduce the losses of N₂O to the atmosphere, but field studies have shown that their efficiency varies depending greatly on the environmental conditions. Soil water content and temperature are key factors controlling N₂O emissions from soils and they seem to be also key parameters responsible for the variation in nitrification inhibitors efficiency. We present a laboratory study aimed at evaluating the effectiveness of the nitrification inhibitor 3,4-dimethylpyrazol phosphate (DMPP) at three different temperatures (10, 15 and 20 °C) and three soil water contents (40%, 60% and 80% of WFPS) on N₂O emissions following the application of 1.2 mg N kg⁻¹ dry soil (equivalent to 140 kg N ha⁻¹). Also the CO₂ and CH₄ emissions were followed to see the possible side effects of DMPP on the overall microbial activities. Nitrogen was applied either as ammonium sulfate nitrate (ASN) or as ENTEC 26 (ASN + DMPP). The application of ENTEC 26 was effective reducing N₂O losses up to the levels of an unfertilized control treatment in all conditions. Nevertheless, the percentage of reduction induced by DMPP in the ENTEC treatment with respect to the ASN varied from 3% to 45% depending on temperature and soil water content conditions. At 40% of WFPS, when nitrification is expected to be the main process producing N₂O, the increase of N₂O emissions in ASN together with temperature provoked an increase in DMPP efficiency reducing these emissions from 17% up to 42%. Contrarily, at 80% of WFPS, when denitrification is expected to be the main source of N₂O, emissions after ASN application decreased with temperature, which induced a decrease from 45% to 23% in the efficiency of DMPP reducing N₂O losses. Overall, the results obtained in this study suggest that DMPP performance regarding N₂O emissions reduction would be the best in cold and wet conditions. Neither CO₂ emissions nor CH₄ emissions were affected by the use of DMPP at the different soil water contents and temperatures.     

Effect of silicate fertilizer on reducing methane emission during rice cultivation

Slag-type silicate fertilizer, which contains high amount of active iron oxide, a potential source of electron acceptor, was applied at the rate of 0, 2, 6, 10, and 20 Mg ha⁻¹ to reduce methane (CH₄) emission from rice planted in potted soils. Methane emission rates measured by closed chamber method decreased significantly with increasing levels of silicate fertilizer application during rice cultivation. Soil redox potential (Eh) decreased rapidly after flooding, but floodwater pH and soil pH increased significantly with increasing levels of silicate fertilizer application. Iron concentrations in potted soils and in percolated water significantly increased with the increasing levels of silicate fertilizer application, which acted as oxidizing agents and electron acceptors, and thereby suppressed CH₄ emissions. Silicate fertilization significantly decreased CH₄ production activity, while it increased carbon dioxide (CO₂) production activity. Rice plant growth, yield parameters, and grain yield were positively influenced by silicate application levels. The maximum increase in grain yield (17% yield increase over the control) was found with 10 Mg ha⁻¹ silicate application along with 28% reduction in total CH₄ flux during rice cultivation. It is, therefore, concluded that slag-type silicate fertilizer could be a suitable soil amendment for reducing CH₄ emissions as well as sustaining rice productivity and restoring the soil nutrient balance in rice paddy soil.     

Influence of water table level and soil properties on emissions of greenhouse gases from cultivated peat soil

A lysimeter method using undisturbed soil columns was used to investigate the effect of water table depth and soil properties on soil organic matter decomposition and greenhouse gas (GHG) emissions from cultivated peat soils. The study was carried out using cultivated organic soils from two locations in Sweden: Örke, a typical cultivated fen peat with low pH and high organic matter content and Majnegården, a more uncommon fen peat type with high pH and low organic matter content. Even though carbon and nitrogen contents differ greatly between the sites, carbon and nitrogen density are quite similar. A drilling method with minimal soil disturbance was used to collect 12 undisturbed soil monoliths (50 cm high, Ø29.5 cm) per site. They were sown with ryegrass (Lolium perenne) after the original vegetation was removed. The lysimeter design allowed the introduction of water at depth so as to maintain a constant water table at either 40 cm or 80 cm below the soil surface. CO₂, CH₄ and N₂O emissions from the lysimeters were measured weekly and complemented with incubation experiments with small undisturbed soil cores subjected to different tensions (5, 40, 80 and 600 cm water column). CO₂ emissions were greater from the treatment with the high water table level (40 cm) compared with the low level (80 cm). N₂O emissions peaked in springtime and CH₄ emissions were very low or negative. Estimated GHG emissions during one year were between 2.70 and 3.55 kg CO₂ equivalents m⁻². The results from the incubation experiment were in agreement with emissions results from the lysimeter experiments. We attribute the observed differences in GHG emissions between the soils to the contrasting dry matter liability and soil physical properties. The properties of the different soil layers will determine the effect of water table regulation. Lowering the water table without exposing new layers with easily decomposable material would have a limited effect on emission rates.     

Potential short-term effects of yak and Tibetan sheep dung on greenhouse gas emissions in two alpine grassland soils under laboratory conditions

Yak and Tibetan sheep graze extensively on natural grasslands in the Qinghai-Tibetan Plateau, and large amounts of excrement are directly deposited onto alpine grasslands. However, information on greenhouse gas (GHG) emissions from this excrement is limited. This study evaluated the short-term effects of yak and Tibetan sheep dung on nitrous oxide (N₂O), methane (CH₄), and carbon dioxide (CO₂) emissions from alpine steppe soil at a water holding capacity (WHC) of 40 or 60 % and from alpine meadow soil at a WHC of 60 or 80 % under laboratory conditions. Cumulative N₂O emissions over a 15-day incubation period at low soil moisture conditions ranged from 111 to 232 μg N₂O–N kg soil^?1 in the yak dung treatments, significantly (P?<?0.01) higher than that of sheep dung treatments (28.7 to 33.7 μg N₂O–N kg soil^?1) and untreated soils (1.04–6.94 μg N₂O–N kg soil^?1). At high soil moisture conditions, N₂O emissions were higher from sheep dung than yak dung and non-treated soils. No significant difference was found between the yak dung and non-treated alpine meadow soil at 80 % WHC. Low N₂O emission in the yak dung treatment from relatively wet soil was probably due to complete denitrification to N₂. Yak dung markedly (P?<?0.001) increased CH₄ and CO₂ emissions, likely being the main source of these two gases. The addition of sheep dung markedly (P?<?0.001) elevated CO₂ emissions. Dung application significantly (P?<?0.01) increased global warming potential, particularly for alpine steppe soil. In conclusion, our findings suggest that yak and Tibetan sheep dung deposited on alpine grassland soils may increase GHG emissions.     

Studies of Soils, Soil Water and Stream Water at a Small Catchment near Guiyang, China

Acid deposition is considered to be a major environmental problem in China, but information about effects on soils and waters is scarce. To contribute to increased knowledge about the problem a small catchment (about 7 ha) in the outskirts of Guiyang, the provincial capital of Guizhou in south-western China, was instrumented for collection of precipitation, throughfall, soil water and stream water. In addition soil samples have been collected and analyzed for key properties. Median pH in the precipitation is 4.40 (quartiles: 4.19 and 4.77) and the median sulfate concentration 228 µeq/L (quartiles: 147 and 334 µeq/L). The dry deposition of both SO₂ and alkaline dust is considerable. The sum of wet deposition of sulfate and dry deposition of SO₂ has been estimated to about 8.5 gSm^-2yr^-1. The total S-deposition may be somewhat higher due to dry deposition of sulfate and occult deposition. In soil water, SO₄ ^2- is the major anion, generally ranging from 300 to 2500 µeq/L in the different plots. Calcium is an important cation, but there is also a considerable contribution of aluminum from the soil. In some of the plots the concentrations of inorganic monomeric aluminum (Ali) are typically between 200 and 400 µm. Potential harmful levels of aluminum and/or high Ali/(Ca²⁺ + Mg²⁺) molar ratios occur in the catchment, but damages to vegetation have not yet been reported. In most cases exchangeable aluminum accounts for between 75 and 95% of the total effective cation exchange capacity (CEC_E) in the mineral soils. The aluminum chemistry cannot easily be explained by conventional models as the Gaines-Thomas ion-exchange equation or equilibrium with an Al(OH)₃ mineral phase. The stream water is generally less acidic and has considerably lower concentrations of aluminum than the soil water, even though quite acid events have been observed (pH < 4.4). The median pH values are 4.9 and 5.0 in the two first order streams and 6.3 in the dam at the lower boarder of the catchment.     

The effect of reduced tillage on nitrous oxide emissions of silt loam soils

The effect of reduced tillage (RT) on nitrous oxide (N₂O) emissions of soils from fields with root crops under a temperate climate was studied. Three silt loam fields under RT agriculture were compared with their respective conventional tillage (CT) field with comparable crop rotation and manure application. Undisturbed soil samples taken in September 2005 and February 2006 were incubated under laboratory conditions for 10 days. The N₂O emission of soils taken in September 2005 varied from 50 to 1,095 μg N kg⁻¹ dry soil. The N₂O emissions of soils from the RT fields taken in September 2005 were statistically (P < 0.05) higher or comparable than the N₂O emissions from their respective CT soil. The N₂O emission of soils taken in February 2006 varied from 0 to 233 μg N kg⁻¹ dry soil. The N₂O emissions of soils from the RT fields taken in February 2006 tended to be higher than the N₂O emissions from their respective CT soil. A positive and significant Pearson correlation of the N₂O–N emissions with nitrate nitrogen (NO₃ ⁻–N) content in the soil was found (P < 0.01). Leaving the straw on the field, a typical feature of RT, decreased NO₃ ⁻–N content of the soil and reduced N₂O emissions from RT soils.     

Response of spodic B horizons to acid precipitation in northernmost Fennoscandia

In northernmost Fennoscandia there is concern about the possible environmental effects of the sulphur emissions from Russian nickel smelters on the Kola Peninsula. The purpose of this study was to investigate to what extent the soils of this region may delay the response to pH changes through sulphate adsorption, and whether there are evidence for strong soil acidification effects. To this end 26 spodic B horizons were collected along a transect from northernmost Sweden to north-easternmost Norway, only 10 km from the Pechenganikel smelter. As the pH(H₂O) was > 4.8 in all soils, and as the exchangeable Ca/Al ratio was high, there were no evidence for strong soil acidification effects. Water-extractable SO₄ was clearly affected by the S deposition and thus SO₄ was at least partly mobile in the soils; it is therefore possible that soil solutions close to the smelter may have been acidified. In spite of this, sulphate adsorption was found to be more important than cation exchange reactions as a delaying process against soil acidification, at least in the top 10 cm of the B horizon. For the top 20 cm of the B horizon it was estimated that S04 adsorption can neutralize, on average, 700 mmol_c, m^?2 of acid before the pH is decreased to 4.4. Thus if the S deposition remains unchanged, decades are required to severely acidify most soils in the affected parts of Norway and Finland.     

Effects of biochar amendment on greenhouse gas emissions,net ecosystem carbon budget and properties of an acidic soil under intensive vegetable production

Biochar addition to soils has been frequently proposed as a means to increase soil fertility and carbon (C) sequestration. However, the effect of biochar addition on greenhouse gas emissions from intensively managed soils under vegetable production at the field scale is poorly understood. The effects of wheat straw biochar amendment with mineral fertilizer or an enhanced‐efficiency fertilizer (mixture of urea and nitrapyrin) on N₂O efflux and the net ecosystem C budget were investigated for an acidic soil in southeast China over a 1‐yr period. Biochar addition did not affect the annual N₂O emissions (26–28 kg N/ha), but reduced seasonal N₂O emissions during the cold period. Biochar increased soil organic C and CO₂ efflux on average by 61 and 19%, respectively. Biochar addition greatly increased C gain in the acidic soil (average 11.1 Mg C/ha) compared with treatments without biochar addition (average ?2.2 Mg C/ha). Biochar amendment did not increase yield‐scaled N₂O emissions after application of mineral fertilizer, but it decreased yield‐scaled N₂O by 15% after nitrapyrin addition. Our results suggest that biochar amendment of acidic soil under intensive vegetable cultivation contributes to soil C sequestration, but has only small effects on both plant growth and greenhouse gas emissions.     

Nitrous oxide emissions from a rainfed-cultivated black soil in Northeast China: effect of fertilization and maize crop

Nitrous oxide emission (N₂O) from applied fertilizer across the different agricultural landscapes especially those of rainfed area is extremely variable (both spatially and temporally), thus posing the greatest challenge to researchers, modelers, and policy makers to accurately predict N₂O emissions. Nitrous oxide emissions from a rainfed, maize-planted, black soil (Udic Mollisols) were monitored in the Harbin State Key Agroecological Experimental Station (Harbin, Heilongjiang Province, China). The four treatments were: a bare soil amended with no N (C0) or with 225?kg?N ha^?1 (CN), and maize (Zea mays L.)-planted soils fertilized with no N (P0) or with 225?kg?N ha^?1 (PN). Nitrous oxide emissions significantly (P?<?0.05) increased from 141?±?5?g N₂O-N?ha^?1 (C0) to 570?±?33?g N₂O-N?ha^?1 (CN) in unplanted soil, and from 209?±?29?g N₂O-N?ha^?1 (P0) to 884?±?45?g N₂O-N?ha^?1 (PN) in planted soil. Approximately 75?% of N₂O emissions were from fertilizer N applied and the emission factor (EF) of applied fertilizer N as N₂O in unplanted and planted soils was 0.19 and 0.30?%, respectively. The presence of maize crop significantly (P?<?0.05) increased the N₂O emission by 55?% in the N-fertilized soil but not in the N-unfertilized soil. There was a significant (P?<?0.05) interaction effect of fertilization?×?maize on N₂O emissions. Nitrous oxide fluxes were significantly affected by soil moisture and soil temperature (P?<?0.05), with the temperature sensitivity of 1.73–2.24, which together explained 62–76?% of seasonal variation in N₂O fluxes. Our results demonstrated that N₂O emissions from rainfed arable black soils in Northeast China primarily depended on the application of fertilizer N; however, the EF of fertilizer N as N₂O was low, probably due to low precipitation and soil moisture.     

Direct experimental evidence for the contribution of lime to CO2 release from managed peat soil

Liming is a common management practice used to achieve optimum pH for plant growth in agricultural soils. Addition of lime to the soil, however, may cause CO₂ release when the carbonates in lime dissolve in water. Although lime may thereby constitute a significant carbon source, especially under acidic soil conditions, experimental data on the CO₂ release are lacking so far. We conducted a split-plot experiment within a cut-away peatland cultivated with a bioenergy crop (reed canary grass, Phalaris arundinacea L.) with lime and fertilizer treatments to determine effects of lime on the CO₂ emissions from soil and to better understand mechanisms underlying liming effects. Carbon dioxide release was measured over two growing seasons in the field after liming, and complementary laboratory studies were conducted. To differentiate CO₂ derived from lime and biotic respiration the δ¹³C of CO₂ released was determined and the two-pool mixing model was applied. The results showed that lime may contribute significantly to CO₂ release from the soil. In the laboratory, more than 50% of CO₂ release was attributable to lime-carbonates during short-term incubation. Lime-derived CO₂ emissions were much lower in the field, and were only detected during the first (2–4) months after the application. However, a maximum of 12% of monthly CO₂ emissions from the cultivated peatland originated from the lime. Biotic respiration rates were similar in limed and unlimed soils, suggesting that higher pH did not, at least in the short-term, increase carbon losses from cultivated peat soils. Additional fertilization and acidification did not contribute to further CO₂ release from the lime. According to our first estimations about one sixth of the lime applied would be released as CO₂ from the managed peatland, with all lime-derived emissions occurring during the first year of application (equivalent to about 4.6% of the total annual CO₂ losses from the soil in the first year). This suggests that the mass-balance approach as proposed by the IPCC Tier 1 methodology, which assumes that all carbon in lime ends up as CO₂ in the atmosphere, overestimates the emissions from lime. Our study further shows that there is a great risk to overestimate heterotrophic microbial activity in limed soils by measuring the CO₂ release without separating abiotic and biotic CO₂ production.