Terrestrial nitrogen–carbon cycle interactions at the global scale

Interactions between the terrestrial nitrogen (N) and carbon (C) cycles shape the response of ecosystems to global change. However, the global distribution of nitrogen availability and its importance in global biogeochemistry and biogeochemical interactions with the climate system remain uncertain. Based on projections of a terrestrial biosphere model scaling ecological understanding of nitrogen–carbon cycle interactions to global scales, anthropogenic nitrogen additions since 1860 are estimated to have enriched the terrestrial biosphere by 1.3 Pg N, supporting the sequestration of 11.2 Pg C. Over the same time period, CO₂ fertilization has increased terrestrial carbon storage by 134.0 Pg C, increasing the terrestrial nitrogen stock by 1.2 Pg N. In 2001–2010, terrestrial ecosystems sequestered an estimated total of 27 Tg N yr⁻¹ (1.9 Pg C yr⁻¹), of which 10 Tg N yr⁻¹ (0.2 Pg C yr⁻¹) are due to anthropogenic nitrogen deposition. Nitrogen availability already limits terrestrial carbon sequestration in the boreal and temperate zone, and will constrain future carbon sequestration in response to CO₂ fertilization (regionally by up to 70% compared with an estimate without considering nitrogen–carbon interactions). This reduced terrestrial carbon uptake will probably dominate the role of the terrestrial nitrogen cycle in the climate system, as it accelerates the accumulation of anthropogenic CO₂ in the atmosphere. However, increases of N₂O emissions owing to anthropogenic nitrogen and climate change (at a rate of approx. 0.5 Tg N yr⁻¹ per 1°C degree climate warming) will add an important long-term climate forcing.     

Carbon Sequestration in Reclaimed Minesoils

Minesoils are drastically influenced by anthropogenic activities. They are characterized by low soil organic matter (SOM) content, low fertility, and poor physicochemical and biological properties, limiting their quality, capability, and functions. Reclamation of these soils has potential for resequestering some of the C lost and mitigating CO₂ emissions. Soil organic carbon (SOC) sequestration rates in minesoils are high in the first 20 to 30 years after reclamation in the top 15 cm soil depth. In general, higher rates of SOC sequestration are observed for minesoils under pasture and grassland management than under forest land use. Observed rates of SOC sequestration are 0.3 to 1.85 Mg C ha^{? 1} yr^{? 1} for pastures and rangelands, and 0.2 to 1.64 Mg C ha^{? 1} yr^{? 1} for forest land use. Proper reclamation and postreclamation management may enhance SOC sequestration and add to the economic value of the mined sites. Management practices that may enhance SOC sequestration include increasing vegetative cover by deep-rooted perennial vegetation and afforestation, improving soil fertility, and alleviation of physical, chemical and biological limitations by fertilizers and soil amendments such as biosolids, manure, coal combustion by-products, and mulches. Soil and water conservation are important to SOC sequestration. The potential of SOC sequestration in minesoils of the US is estimated to be 1.28 Tg C yr^?1, compared to the emissions from coal combustion of 506 Tg C yr^{? 1}.     

Soil carbon sequestrations by nitrogen fertilizer application, straw return and no-tillage in China's cropland

Soil as the largest global carbon pool has played a great role in sequestering the atmospheric carbon dioxide (CO₂). Although global carbon sequestration potentials have been assessed since the 1980s, few investigations have been made on soil carbon sequestration (SCS) in China's cropland. China is a developing country and has a long history of agricultural activities. Estimation of SCS potentials in China's cropland is very important for assessing the potential measures to prevent the atmospheric carbon rise and predicting the atmospheric CO₂ concentration in future. After review of the available results of the field experiments in China, relationships between SCS and nitrogen fertilizer application, straw return and no‐tillage (NT) practices were established for each of the four agricultural regions. According to the current agricultural practices and their future development, estimations were made on SCS by nitrogen fertilizer application, straw return and NT in China's cropland. In the current situation, nitrogen fertilizer application, straw return and zero tillage can sequester 5.96, 9.76 and 0.800 Tg C each year. Carbon sequestration potential will increase to 12.1 Tg C yr⁻¹ if nitrogen is fertilized on experts' recommendations. The carbon sequestration potentials of straw return and NT can reach 34.4 and 4.60 Tg C yr⁻¹ when these two techniques are further popularized. In these measures, straw return is the most promising one. Full popularization of straw return can reduce 5.3% of the CO₂ emission from fossil fuel combustion in China in 1990, which meets the global mean CO₂ reduction requested by the Kyoto Protocol (5.2%). In general, if more incentive policies can be elaborated and implemented, the SCS in China's cropland will be increased by about two times. So, popularization of the above‐mentioned agricultural measures for carbon sequestration can be considered as an effective tool to prevent the rapid rise of the atmospheric CO₂ in China.     

A new estimation of global soil greenhouse gas fluxes using a simple data-oriented model

Soil greenhouse gas fluxes (particularly CO₂, CH₄, and N₂O) play important roles in climate change. However, despite the importance of these soil greenhouse gases, the number of reports on global soil greenhouse gas fluxes is limited. Here, new estimates are presented for global soil CO₂ emission (total soil respiration), CH₄ uptake, and N₂O emission fluxes, using a simple data-oriented model. The estimated global fluxes for CO₂ emission, CH₄ uptake, and N₂O emission were 78 Pg C yr⁻¹ (Monte Carlo 95% confidence interval, 64–95 Pg C yr⁻¹), 18 Tg C yr⁻¹ (11–23 Tg C yr⁻¹), and 4.4 Tg N yr⁻¹ (1.4–11.1 Tg N yr⁻¹), respectively. Tropical regions were the largest contributor of all of the gases, particularly the CO₂ and N₂O fluxes. The soil CO₂ and N₂O fluxes had more pronounced seasonal patterns than the soil CH₄ flux. The collected estimates, including both the previous and the present estimates, demonstrate that the means of the best estimates from each study were 79 Pg C yr⁻¹ (291 Pg CO₂ yr⁻¹; coefficient of variation, CV = 13%, N = 6) for CO₂, 21 Tg C yr⁻¹ (29 Tg CH₄ yr⁻¹; CV = 24%, N = 24) for CH₄, and 7.8 Tg N yr⁻¹ (12.2 Tg N₂O yr⁻¹; CV = 38%, N = 11) for N₂O. For N₂O, the mean of the estimates that was calculated by excluding the earliest two estimates was 6.6 Tg N yr⁻¹ (10.4 Tg N₂O yr⁻¹; CV = 22%, N = 9). The reported estimates vary and have large degrees of uncertainty but their overall magnitudes are in general agreement. To further minimize the uncertainty of soil greenhouse gas flux estimates, it is necessary to build global databases and identify key processes in describing global soil greenhouse gas fluxes.     

Interactions between plant growth and soil nutrient cycling under elevated CO2: a meta-analysis

free air carbon dioxide enrichment (FACE) and open top chamber (OTC) studies are valuable tools for evaluating the impact of elevated atmospheric CO₂ on nutrient cycling in terrestrial ecosystems. Using meta‐analytic techniques, we summarized the results of 117 studies on plant biomass production, soil organic matter dynamics and biological N₂ fixation in FACE and OTC experiments. The objective of the analysis was to determine whether elevated CO₂ alters nutrient cycling between plants and soil and if so, what the implications are for soil carbon (C) sequestration. Elevated CO₂ stimulated gross N immobilization by 22%, whereas gross and net N mineralization rates remained unaffected. In addition, the soil C : N ratio and microbial N contents increased under elevated CO₂ by 3.8% and 5.8%, respectively. Microbial C contents and soil respiration increased by 7.1% and 17.7%, respectively. Despite the stimulation of microbial activity, soil C input still caused soil C contents to increase by 1.2% yr^?1. Namely, elevated CO₂ stimulated overall above‐ and belowground plant biomass by 21.5% and 28.3%, respectively, thereby outweighing the increase in CO₂ respiration. In addition, when comparing experiments under both low and high N availability, soil C contents (+2.2% yr^?1) and above‐ and belowground plant growth (+20.1% and+33.7%) only increased under elevated CO₂ in experiments receiving the high N treatments. Under low N availability, above‐ and belowground plant growth increased by only 8.8% and 14.6%, and soil C contents did not increase. Nitrogen fixation was stimulated by elevated CO₂ only when additional nutrients were supplied. These results suggest that the main driver of soil C sequestration is soil C input through plant growth, which is strongly controlled by nutrient availability. In unfertilized ecosystems, microbial N immobilization enhances acclimation of plant growth to elevated CO₂ in the long‐term. Therefore, increased soil C input and soil C sequestration under elevated CO₂ can only be sustained in the long‐term when additional nutrients are supplied.     

Long‐term impacts of manure amendments on carbon and greenhouse gas dynamics of rangelands

Livestock manure is applied to rangelands as an organic fertilizer to stimulate forage production, but the long‐term impacts of this practice on soil carbon (C) and greenhouse gas (GHG) dynamics are poorly known. We collected soil samples from manured and nonmanured fields on commercial dairies and found that manure amendments increased soil C stocks by 19.0 ± 7.3 Mg C ha^?1 and N stocks by 1.94 ± 0.63 Mg N ha^?1 compared to nonmanured fields (0–20 cm depth). Long‐term historical (1700–present) and future (present–2100) impacts of management on soil C and N dynamics, net primary productivity (NPP), and GHG emissions were modeled with DayCent. Modeled total soil C and N stocks increased with the onset of dairying. Nitrous oxide (N₂O) emissions also increased by ~2 kg N₂O‐N ha^?1 yr^?1. These emissions were proportional to total N additions and offset 75–100% of soil C sequestration. All fields were small net methane (CH₄) sinks, averaging ?4.7 ± 1.2 kg CH₄‐C ha^?1 yr^?1. Overall, manured fields were net GHG sinks between 1954 and 2011 (?0.74 ± 0.73 Mg CO₂ e ha^?1 yr^?1, CO₂e are carbon dioxide equivalents), whereas nonmanured fields varied around zero. Future soil C pools stabilized 40–60 years faster in manured fields than nonmanured fields, at which point manured fields were significantly larger sources than nonmanured fields (1.45 ± 0.52 Mg CO₂e ha^?1 yr^?1 and 0.51 ± 0.60 Mg CO₂e ha^?1 yr^?1, respectively). Modeling also revealed a large background loss of soil C from the passive soil pool associated with the shift from perennial to annual grasses, equivalent to 29.4 ± 1.47 Tg CO₂e in California between 1820 and 2011. Manure applications increased NPP and soil C storage, but plant community changes and GHG emissions decreased, and eventually eliminated, the net climate benefit of this practice.     

China's crop productivity and soil carbon storage as influenced by multifactor global change

Much concern has been raised about how multifactor global change has affected food security and carbon sequestration capacity in China. By using a process‐based ecosystem model, the Dynamic Land Ecosystem Model (DLEM), in conjunction with the newly developed driving information on multiple environmental factors (climate, atmospheric CO₂, tropospheric ozone, nitrogen deposition, and land cover/land use change), we quantified spatial and temporal patterns of net primary production (NPP) and soil organic carbon storage (SOC) across China's croplands during 1980–2005 and investigated the underlying mechanisms. Simulated results showed that both crop NPP and SOC increased from 1980 to 2005, and the highest annual NPP occurred in the Southeast (SE) region (0.32 Pg C yr^?1, 35.4% of the total NPP) whereas the largest annual SOC (2.29 Pg C yr^?1, 35.4% of the total SOC) was found in the Northeast (NE) region. Land management practices, particularly nitrogen fertilizer application, appear to be the most important factor in stimulating increase in NPP and SOC. However, tropospheric ozone pollution and climate change led to NPP reduction and SOC loss. Our results suggest that China's crop productivity and soil carbon storage could be enhanced through minimizing tropospheric ozone pollution and improving nitrogen fertilizer use efficiency.     

Potential Soil Carbon Sequestration and CO2 Offset by Dedicated Energy Crops in the USA

Energy crops are fast-growing species whose biomass yields are dedicated to the production of more immediately usable energy forms, such as liquid fuels or electricity. Biomass-based energy sources can offset, or displace, some amount of fossil-fuel use. Energy derived from biomass provides 2 to 3% of the energy used in the U.S.A.; but, with the exception of corn-(Zea mays L.)-to-ethanol, very little energy is currently derived from dedicated energy crops. In addition to the fossil-fuel offset, energy cropping might also mitigate an accentuated greenhouse gas effect by causing a net sequestration of atmospheric C into soil organic C (SOC). Energy plantations of short-rotation woody crops (SRWC) or herbaceous crops (HC) can potentially be managed to favor SOC sequestration. This review is focused primarily on the potential to mitigate atmospheric CO₂ emissions by fostering SOC sequestration in energy cropping systems deployed across the landscape in the United States. We know that land use affects the dynamics of the SOC pool, but data about spatial and temporal variability in the SOC pool under SRWC and HC are scanty due to lack of well-designed, long-term studies. The conventional methods of studying SOC fluxes involve paired-plot designs and chronosequences, but isotopic techniques may also be feasible in understanding temporal changes in SOC. The rate of accumulation of SOC depends on land-use history, soil type, vegetation type, harvesting cycle, and other management practices. The SOC pool tends to be enhanced more under deep-rooted grasses, N-fixers, and deciduous species. Carbon sequestration into recalcitrant forms in the SOC pool can be enhanced with some management practices (e.g., conservation tillage, fertilization, irrigation); but those practices can carry a fossil-C cost. Reported rates of SOC sequestration range from 0 to 1.6 Mg C ha^?1 yr^?1 under SRWC and 0 to 3 Mg C ha^?1 yr^?1 under HC. Production of 5 EJ of electricity from energy crops—a perhaps reasonable scenario for the U.S.A.—would require about 60 Mha. That amount of land is potentially available for conversion to energy plantations in the U.S.A. The land so managed could mitigate C emissions (through fossil C not emitted and SOC sequestered) by about 5.4 Mg C ha^?1 yr^?1. On 60 Mha, that would represent 324 Tg C yr^?1—a 20% reduction from current fossil-fuel CO₂ emissions. Advances in productivity of fast-growing SRWC and HC species suggest that deployment of energy cropping systems could be an effective strategy to reduce climate-altering effects of anthropogenic CO₂ emissions and to meet global policy commitments.     

The impact of nitrogen deposition on carbon sequestration in European forests and forest soils

An estimate of net carbon (C) pool changes and long‐term C sequestration in trees and soils was made at more than 100 intensively monitored forest plots (level II plots) and scaled up to Europe based on data for more than 6000 forested plots in a systematic 16 km × 16 km grid (level I plots). C pool changes in trees at the level II plots were based on repeated forest growth surveys At the level I plots, an estimate of the mean annual C pool changes was derived from stand age and available site quality characteristics. C sequestration, being equal to the long‐term C pool changes accounting for CO₂ emissions because of harvest and forest fires, was assumed 33% of the overall C pool changes by growth. C sequestration in the soil were based on calculated nitrogen (N) retention (N deposition minus net N uptake minus N leaching) rates in soils, multiplied by the C/N ratio of the forest soils, using measured data only (level II plots) or a combination of measurements and model calculations (level I plots). Net C sequestration by forests in Europe (both trees and soil) was estimated at 0.117 Gton yr^?1, with the C sequestration in stem wood being approximately four times as high (0.094 Gton yr^?1) as the C sequestration in the soil (0.023 Gton yr^?1). The European average impact of an additional N input on the net C sequestration was estimated at approximately 25 kg C kg^?1 N for both tree wood and soil. The contribution of an average additional N deposition on European forests of 2.8 kg ha^?1 yr^?1 in the period 1960–2000 was estimated at 0.0118 Gton yr^?1, being equal to 10% of the net C sequestration in both trees and soil in that period (0.117 Gton yr^?1). The C sequestration in trees increased from Northern to Central Europe, whereas the C sequestration in soil was high in Central Europe and low in Northern and Southern Europe. The result of this study implies that the impact of forest management on tree growth is most important in explaining the C pool changes in European forests.     

Estimation of nitrous oxide, nitric oxide and ammonia emissions from croplands in East, Southeast and South Asia

Agricultural activities have greatly altered the global nitrogen (N) cycle and produced nitrogenous gases of environmental significance. More than half of all chemical N fertilizer produced globally is used in crop production in East, Southeast and South Asia, where rice is central to nutrition. Emissions of nitrous oxide (N₂O), nitric oxide (NO) and ammonia (NH₃) from croplands in this region were estimated by considering background emission and emissions resulting from N added to croplands, including chemical N, animal manure, biologically fixed N and N in crop residues returned to fields. Background emission fluxes of N₂O and NO from croplands were estimated to be 1.22 and 0.57 kg N ha^?1 yr^?1, respectively. Separate fertilizer‐induced emission factors were estimated for upland fields and rice fields. Total N₂O emission from croplands in the study region was estimated to be 1.19 Tg N yr^?1, with 43% contributed by background emissions. The average fertilizer‐induced N₂O emission, however, accounts for only 0.93% of the applied N, which is less than the default IPCC value of 1.25%, because of the low emission factor from paddy fields. Total NO emission was 591 Gg N yr^?1 in the study region, with 40% from background emissions. The average fertilizer‐induced NO emission factor was 0.48%. Total NH₃ emission was estimated to be 11.8 Tg N yr^?1. The use of urea and ammonium bicarbonate and the cultivation of rice led to a high average NH₃ loss rate from chemical N fertilizer in the study region. Emissions were displayed at a 0.5° × 0.5° resolution with the use of a global landuse database.     

Intercropping enhances soil carbon and nitrogen

Intercropping, the simultaneous cultivation of multiple crop species in a single field, increases aboveground productivity due to species complementarity. We hypothesized that intercrops may have greater belowground productivity than sole crops, and sequester more soil carbon over time due to greater input of root litter. Here, we demonstrate a divergence in soil organic carbon (C) and nitrogen (N) content over 7 years in a field experiment that compared rotational strip intercrop systems and ordinary crop rotations. Soil organic C content in the top 20 cm was 4% ± 1% greater in intercrops than in sole crops, indicating a difference in C sequestration rate between intercrop and sole crop systems of 184 ± 86 kg C ha^?1 yr^?1. Soil organic N content in the top 20 cm was 11% ± 1% greater in intercrops than in sole crops, indicating a difference in N sequestration rate between intercrop and sole crop systems of 45 ± 10 kg N ha^?1 yr^?1. Total root biomass in intercrops was on average 23% greater than the average root biomass in sole crops, providing a possible mechanism for the observed divergence in soil C sequestration between sole crop and intercrop systems. A lowering of the soil δ¹⁵N signature suggested that increased biological N fixation and/or reduced gaseous N losses contributed to the increases in soil N in intercrop rotations with faba bean. Increases in soil N in wheat/maize intercrop pointed to contributions from a broader suite of mechanisms for N retention, e.g., complementary N uptake strategies of the intercropped plant species. Our results indicate that soil C sequestration potential of strip intercropping is similar in magnitude to that of currently recommended management practises to conserve organic matter in soil. Intercropping can contribute to multiple agroecosystem services by increased yield, better soil quality and soil C sequestration.     

Estimating soil carbon sequestration under elevated CO2 by combining carbon isotope labelling with soil carbon cycle modelling

Elevated CO₂ concentrations generally stimulate grassland productivity, but herbaceous plants have only a limited capacity to sequester extra carbon (C) in biomass. However, increased primary productivity under elevated CO₂ could result in increased transfer of C into soils where it could be stored for prolonged periods and exercise a negative feedback on the rise in atmospheric CO₂. Measuring soil C sequestration directly is notoriously difficult for a number of methodological reasons. Here, we present a method that combines C isotope labelling with soil C cycle modelling to partition net soil sequestration into changes in new C fixed over the experimental duration (C_new) and pre‐experimental C (C_old). This partitioning is advantageous because the C_new accumulates whereas C_old is lost in the course of time (ΔC_new>0 whereas ΔC_old<0). We applied this method to calcareous grassland exposed to 600 μL CO₂ L^?1 for 6 years. The CO₂ used for atmospheric enrichment was depleted in ¹³C relative to the background atmosphere, and this distinct isotopic signature was used to quantify net soil C_new fluxes under elevated CO₂. Using ¹³C/¹²C mass balance and inverse modelling, the Rothamsted model ‘RothC’ predicted gross soil C_new inputs under elevated CO₂ and the decomposition of C_old. The modelled soil C pools and fluxes were in good agreement with experimental data. C isotope data indicated a net sequestration of ≈90 g C_new m^?2 yr^?1 in elevated CO₂. Accounting for C_old‐losses, this figure was reduced to ≈30 g C m^?2 yr^?1 at elevated CO₂; the elevated CO₂‐effect on net C sequestration was in the range of≈10 g C m^?2 yr^?1. A sensitivity and error analysis suggests that the modelled data are relatively robust. However, elevated CO₂‐specific mechanisms may necessitate a separate parameterization at ambient and elevated CO₂; these include increased soil moisture due to reduced leaf conductance, soil disaggregation as a consequence of increased soil moisture, and priming effects. These effects could accelerate decomposition of C_old in elevated CO₂ so that the CO₂ enrichment effect may be zero or even negative. Overall, our findings suggest that the C sequestration potential of this grassland under elevated CO₂ is rather limited.     

Greenhouse gas fluxes from an Australian subtropical cropland under long‐term contrasting management regimes

The long‐term effects of conservation management practices on greenhouse gas fluxes from tropical/subtropical croplands remain to be uncertain. Using both manual and automatic sampling chambers, we measured N₂O and CH₄ fluxes at a long‐term experimental site (1968–present) in Queensland, Australia from 2006 to 2009. Annual net greenhouse gas fluxes (NGGF) were calculated from the 3‐year mean N₂O and CH₄ fluxes and the long‐term soil organic carbon changes. N₂O emissions exhibited clear daily, seasonal and interannual variations, highlighting the importance of whole‐year measurement over multiple years for obtaining temporally representative annual emissions. Averaged over 3 years, annual N₂O emissions from the unfertilized and fertilized soils (90 kg N ha^?1 yr^?1 as urea) amounted to 138 and 902 g N ha^?1, respectively. The average annual N₂O emissions from the fertilized soil were 388 g N ha^?1 lower under no‐till (NT) than under conventional tillage (CT) and 259 g N ha^?1 higher under stubble retention (SR) than under stubble burning (SB). Annual N₂O emissions from the unfertilized soil were similar between the contrasting tillage and stubble management practices. The average emission factors of fertilizer N were 0.91%, 1.20%, 0.52% and 0.77% for the CT‐SB, CT‐SR, NT‐SB and NT‐SR treatments, respectively. Annual CH₄ fluxes from the soil were very small (?200–300 g CH₄ ha^?1 yr^?1) with no significant difference between treatments. The NGGF were 277–350 kg CO₂‐e ha^?1 yr^?1 for the unfertilized treatments and 401–710 kg CO₂‐e ha^?1 yr^?1 for the fertilized treatments. Among the fertilized treatments, N₂O emissions accounted for 52–97% of NGGF and NT‐SR resulted in the lowest NGGF (401 kg CO₂‐e ha^?1 yr^?1 or 140 kg CO₂‐e t^?1 grain). Therefore, NT‐SR with improved N fertilizer management practices was considered the most promising management regime for simultaneously achieving maximal yield and minimal NGGF.     

Global atmospheric change effects on terrestrial carbon sequestration: Exploration with a global C- and N-cycle model (CQUESTN)

A model of the interacting global carbon and nitrogen cycles (CQUESTN) is developed to explore the possible history of C-sequestration into the terrestrial biosphere in response to the global increases (past and possible future) in atmospheric CO₂ concentration, temperature and N-deposition. The model is based on published estimates of pre-industrial C and N pools and fluxes into vegetation, litter and soil compartments. It was found necessary to assign low estimates of N pools and fluxes to be compatible with the more firmly established C-cycle data. Net primary production was made responsive to phytomass N level, and to CO₂ and temperature deviation from preindustrial values with sensitivities covering the ranges in the literature. Biological N-fixation could be made either unresponsive to soil C:N ratio, or could act to tend to restore the preindustrial C:N of humus with different N-fixation intensities. As for all such simulation models, uncertainties in both data and functional relationships render it more useful for qualitative evaluation than for quantitative prediction.With the N-fixation response turned off, the historic CO₂ increase led to standard-model sequestration into terrestrial ecosystems in 1995AD of 1.8 Gt C yr^–1. With N-fixation restoring humus C:N strongly, C sequestration was 3 Gt yr^–1 in 1995. In both cases C:N of phytomass and litter increased with time and these increases were plausible when compared with experimental data on CO₂ effects. The temperature increase also caused net C sequestration in the model biosphere because decrease in soil organic matter was more than offset by the increase in phytomass deriving from the extra N mineralised. For temperature increase to reduce system C pool size, the biosphere leakiness to N would have to increase substantially with temperature. Assuming a constant N-loss coefficient, the historic temperature increase alone caused standard-model net C sequestration to be about 0.6 Gt C in 1995. Given the disparity of plant and microbial C:N, the modelled impact of anthropogenic N-deposition on C-sequestration depends substantially on whether the deposited N is initially taken up by plants or by soil microorganisms. Assuming the latter, standard-model net sequestration in 1995 was 0.2 Gt C in 1995 from the N-deposition effect alone. Combining the effects of the historic courses of CO₂, temperature and N-deposition, the standard-model gave C-sequestration of 3.5 Gt in 1995. This involved an assumed weak response of biological N-fixation to the increased carbon status of the ecosystem. For N-fixation to track ecosystem C-fixation in the long term however, more phosphorus must enter the biological cycle. New experimental evidence shows that plants in elevated CO₂ have the capacity to mobilize more phosphorus from so-called unavailable sources using mechanisms involving exudation of organic acids and phosphatases.     

Management options for reducing CO2 emissions from agricultural soils

Crop-based agriculture occupies 1.7 billion hectares, globally, with a soil C stock of about 170 Pg. Of the past anthropogenic CO² additions to the atmosphere, about 50 Pg C came from the loss of soil organic matter (SOM) in cultivated soils. Improved management practices, however, can rebuild C stocks in agricultural soils and help mitigate CO² emissions.Increasing soil C stocks requires increasing C inputs and/or reducing soil heterotrophic respiration. Management options that contribute to reduced soil respiration include reduced tillage practices (especially no-till) and increased cropping intensity. Physical disturbance associated with intensive soil tillage increases the turnover of soil aggregates and accelerates the decomposition of aggregate-associated SOM. No-till increases aggregate stability and promotes the formation of recalcitrant SOM fractions within stabilized micro- and macroaggregate structures. Experiments using¹³ C natural abundance show up to a two-fold increase in mean residence time of SOM under no-till vs intensive tillage. Greater cropping intensity, i.e., by reducing the frequency of bare fallow in crop rotations and increasing the use of perennial vegetation, can increase water and nutrient use efficiency by plants, thereby increasing C inputs to soil and reducing organic matter decomposition rates.Management and policies to sequester C in soils need to consider that: soils have a finite capacity to store C, gains in soil C can be reversed if proper management is not maintained, and fossil fuel inputs for different management practices need to be factored into a total agricultural CO² balance.     

Simulated chronic NO3− deposition reduces soil respiration in northern hardwood forests

Chronic N additions to forest ecosystems can enhance soil N availability, potentially leading to reduced C allocation to root systems. This in turn could decrease soil CO₂ efflux. We measured soil respiration during the first, fifth, sixth and eighth years of simulated atmospheric NO₃^? deposition (3 g N m^?2 yr^?1) to four sugar maple‐dominated northern hardwood forests in Michigan to assess these possibilities. During the first year, soil respiration rates were slightly, but not significantly, higher in the NO₃^?‐amended plots. In all subsequent measurement years, soil respiration rates from NO₃^?‐amended soils were significantly depressed. Soil temperature and soil matric potential were measured concurrently with soil respiration and used to develop regression relationships for predicting soil respiration rates. Estimates of growing season and annual soil CO₂ efflux made using these relationships indicate that these C fluxes were depressed by 15% in the eighth year of chronic NO₃^? additions. The decrease in soil respiration was not due to reduced C allocation to roots, as root respiration rates, root biomass, and root turnover were not significantly affected by N additions. Aboveground litter also was unchanged by the 8 years of treatment. Of the remaining potential causes for the decline in soil CO₂ efflux, reduced microbial respiration appears to be the most likely possibility. Documented reductions in microbial biomass and the activities of extracellular enzymes used for litter degradation on the NO₃^?‐amended plots are consistent with this explanation.     

Declining trend of carbon in Finnish cropland soils in 1974–2009

Soil organic matter not only affects soil properties and productivity but also has an essential role in global carbon (C) cycle. We studied changes in the topsoil C content of Finnish croplands using a dataset produced in nationwide soil monitoring. The monitoring network consisting of fields on both mineral and organic soils was established in 1974 and resampled in 1987, 1998, and 2009. Over the monitoring period from 1974 to 2009, cultivated soils showed a continuous decline in C concentration (g kg^?1). In organic soils, C concentration decreased at a mean rate of 0.2–0.3% yr^?1 relative to the existing C concentration. In mineral soils, the relative decrease was 0.4% yr^?1 corresponding to a C stock (kg m^?2) loss of 220 kg ha^?1 yr^?1. The change in management practices in last decades toward increasing cultivation of annual crops has contributed to soil C losses noted in this study. The results, however, suggest that the C losses result partly from other processes affecting cultivated soils such as climatic change or the continuing long‐term effect of forest clearance. We estimated that Finnish cropland soils store 161 Tg carbon nationwide in the topmost 15 cm of which 117 Tg is in mineral soils. C losses from mineral soils can therefore total up to 0.5 Tg yearly.     

Anthropogenic nitrogen deposition in boreal forests has a minor impact on the global carbon cycle

It is proposed that increases in anthropogenic reactive nitrogen (N_r) deposition may cause temperate and boreal forests to sequester a globally significant quantity of carbon (C); however, long‐term data from boreal forests describing how C sequestration responds to realistic levels of chronic N_r deposition are scarce. Using a long‐term (14‐year) stand‐scale (0.1 ha) N addition experiment (three levels: 0, 12.5, and 50 kg N ha⁻¹ yr⁻¹) in the boreal zone of northern Sweden, we evaluated how chronic N additions altered N uptake and biomass of understory communities, and whether changes in understory communities explained N uptake and C sequestration by trees. We hypothesized that understory communities (i.e. mosses and shrubs) serve as important sinks for low‐level N additions, with the strength of these sinks weakening as chronic N addition rates increase, due to shifts in species composition. We further hypothesized that trees would exhibit nonlinear increases in N acquisition, and subsequent C sequestration as N addition rates increased, due to a weakening understory N sink. Our data showed that understory biomass was reduced by 50% in response to the high N addition treatment, mainly due to reduced moss biomass. A ¹⁵N labeling experiment showed that feather mosses acquired the largest fraction of applied label, with this fraction decreasing as the chronic N addition level increased. Contrary to our hypothesis, the proportion of label taken up by trees was equal (ca. 8%) across all three N addition treatments. The relationship between N addition and C sequestration in all vegetation pools combined was linear, and had a slope of 16 kg C kg⁻¹ N. While canopy retention of N_r deposition may cause C sequestration rates to be slightly different than this estimate, our data suggest that a minor quantity of annual anthropogenic CO₂ emissions are sequestered into boreal forests as a result of N_r deposition.     

Dissolved carbon leaching from soil is a crucial component of the net ecosystem carbon balance

Estimates of carbon leaching losses from different land use systems are few and their contribution to the net ecosystem carbon balance is uncertain. We investigated leaching of dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), and dissolved methane (CH₄), at forests, grasslands, and croplands across Europe. Biogenic contributions to DIC were estimated by means of its δ¹³C signature. Leaching of biogenic DIC was 8.3±4.9 g m^?2 yr^?1 for forests, 24.1±7.2 g m^?2 yr^?1 for grasslands, and 14.6±4.8 g m^?2 yr^?1 for croplands. DOC leaching equalled 3.5±1.3 g m^?2 yr^?1 for forests, 5.3±2.0 g m^?2 yr^?1 for grasslands, and 4.1±1.3 g m^?2 yr^?1 for croplands. The average flux of total biogenic carbon across land use systems was 19.4±4.0 g C m^?2 yr^?1. Production of DOC in topsoils was positively related to their C/N ratio and DOC retention in subsoils was inversely related to the ratio of organic carbon to iron plus aluminium (hydr)oxides. Partial pressures of CO₂ in soil air and soil pH determined DIC concentrations and fluxes, but soil solutions were often supersaturated with DIC relative to soil air CO₂. Leaching losses of biogenic carbon (DOC plus biogenic DIC) from grasslands equalled 5–98% (median: 22%) of net ecosystem exchange (NEE) plus carbon inputs with fertilization minus carbon removal with harvest. Carbon leaching increased the net losses from cropland soils by 24–105% (median: 25%). For the majority of forest sites, leaching hardly affected actual net ecosystem carbon balances because of the small solubility of CO₂ in acidic forest soil solutions and large NEE. Leaching of CH₄ proved to be insignificant compared with other fluxes of carbon. Overall, our results show that leaching losses are particularly important for the carbon balance of agricultural systems.     

Preliminary estimates of the potential for carbon mitigation in European soils through no-till farming

In this paper we estimate the European potential for carbon mitigation of no-till farming using results from European tillage experiments. Our calculations suggest some potential in terms of (a) reduced agricultural fossil fuel emissions, and (b) increased soil carbon sequestration. We estimate that 100% conversion to no-till farming would be likely to sequester about 23 Tg C y^–1 in the European Union or about 43 Tg C y^–1 in the wider Europe (excluding the former Soviet Union). In addition, up to 3.2 Tg C y^–1 could be saved in agricultural fossil fuel emissions. Compared to estimates of the potential for carbon sequestration of other carbon mitigation options, no-till agriculture shows nearly twice the potential of scenarios whereby soils are amended with organic materials. Our calculations suggest that 100% conversion to no-till agriculture in Europe could mitigate all fossil fuel-carbon emissions from agriculture in Europe. However, this is equivalent to only about 4.1% of total anthropogenic CO₂-carbon produced annually in Europe (excluding the former Soviet Union) which in turn is equivalent to about 0.8% of global annual anthropogenic CO₂-carbon emissions.