Nitrogen balance in the Trachypogon grasslands of Central Venezuela

The nitrogen balance of a Trachypogon grassland in Calabozo, Venezuela, is calculated for average conditions using biomass accumulation, nitrogen content, and turnover rates of organic matter. Burning Trachypogon grasslands results in losses of 8.5 kg N ha^?1 yr^?1, while rainfall inputs average 2.6 kg N ha^?1 yr^?1. Uptake of N by vegetation is 14.8 kg N ha^?1 yr^?1, but the total N required to build new tissue during a growing season is about 30 kg N ha^?1 yr^?1, so that about 50% of the nitrogen in the vegetation is recycled internally. Nitrogen lossesvia fire are probably balanced by biological N₂-fixation, but no data are available for N-fixation in these savannas. The calculations presented in this paper are based on few data and more measurements are needed to develop a conclusive picture of the N-balance of Trachypogon grasslands.     

High retention of 15N‐labeled nitrogen deposition in a nitrogen saturated old‐growth tropical forest

The effects of increased reactive nitrogen (N) deposition in forests depend largely on its fate in the ecosystems. However, our knowledge on the fates of deposited N in tropical forest ecosystems and its retention mechanisms is limited. Here, we report the results from the first whole ecosystem ¹⁵N labeling experiment performed in a N‐rich old‐growth tropical forest in southern China. We added ¹⁵N tracer monthly as ¹⁵NH₄¹⁵NO₃ for 1 year to control plots and to N‐fertilized plots (N‐plots, receiving additions of 50 kg N ha^?1 yr^?1 for 10 years). Tracer recoveries in major ecosystem compartments were quantified 4 months after the last addition. Tracer recoveries in soil solution were monitored monthly to quantify leaching losses. Total tracer recovery in plant and soil (N retention) in the control plots was 72% and similar to those observed in temperate forests. The retention decreased to 52% in the N‐plots. Soil was the dominant sink, retaining 37% and 28% of the labeled N input in the control and N‐plots, respectively. Leaching below 20 cm was 50 kg N ha^?1 yr^?1 in the control plots and was close to the N input (51 kg N ha^?1 yr^?1), indicating N saturation of the top soil. Nitrogen addition increased N leaching to 73 kg N ha^?1 yr^?1. However, of these only 7 and 23 kg N ha^?1 yr^?1 in the control and N‐plots, respectively, originated from the labeled N input. Our findings indicate that deposited N, like in temperate forests, is largely incorporated into plant and soil pools in the short term, although the forest is N‐saturated, but high cycling rates may later release the N for leaching and/or gaseous loss. Thus, N cycling rates rather than short‐term N retention represent the main difference between temperate forests and the studied tropical forest.     

Nitrogen deposition in tropical forests from savanna and deforestation fires

We used satellite‐derived estimates of global fire emissions and a chemical transport model to estimate atmospheric nitrogen (N) fluxes from savanna and deforestation fires in tropical ecosystems. N emissions and reactive N deposition led to a net transport of N equatorward, from savannas and areas undergoing deforestation to tropical forests. Deposition of fire‐emitted N in savannas was only 26% of emissions – indicating a net export from this biome. On average, net N loss from fires (the sum of emissions and deposition) was equivalent to approximately 22% of biological N fixation (BNF) in savannas (4.0 kg N ha^?1 yr^?1) and 38% of BNF in ecosystems at the deforestation frontier (9.3 kg N ha^?1 yr^?1). Net N gains from fires occurred in interior tropical forests at a rate equivalent to 3% of their BNF (0.8 kg N ha^?1 yr^?1). This percentage was highest for African tropical forests in the Congo Basin (15%; 3.4 kg N ha^?1 yr^?1) owing to equatorward transport from frequently burning savannas north and south of the basin. These results provide evidence for cross‐biome atmospheric fluxes of N that may help to sustain productivity in some tropical forest ecosystems on millennial timescales. Anthropogenic fires associated with slash and burn agriculture and deforestation in the southern part of the Amazon Basin and across Southeast Asia have substantially increased N deposition in these regions in recent decades and may contribute to increased rates of carbon accumulation in secondary forests and other N‐limited ecosystems.     

Effects of experimental nitrogen additions on plant diversity in an old‐growth tropical forest

Response of plant biodiversity to increased availability of nitrogen (N) has been investigated in temperate and boreal forests, which are typically N‐limited, but little is known in tropical forests. We examined the effects of artificial N additions on plant diversity (species richness, density and cover) of the understory layer in an N saturated old‐growth tropical forest in southern China to test the following hypothesis: N additions decrease plant diversity in N saturated tropical forests primarily from N‐mediated changes in soil properties. Experimental additions of N were administered at the following levels from July 2003 to July 2008: no addition (Control); 50 kg N ha^?1 yr^?1 (Low‐N); 100 kg N ha^?1 yr^?1 (Medium‐N), and 150 kg N ha^?1 yr^?1 (High‐N). Results showed that no understory species exhibited positive growth response to any level of N addition during the study period. Although low‐to‐medium levels of N addition (≤100 kg N ha^?1 yr^?1) generally did not alter plant diversity through time, high levels of N addition significantly reduced species diversity. This decrease was most closely related to declines within tree seedling and fern functional groups, as well as to significant increases in soil acidity and Al mobility, and decreases in Ca availability and fine‐root biomass. This mechanism for loss of biodiversity provides sharp contrast to competition‐based mechanisms suggested in studies of understory communities in other forests. Our results suggest that high‐N additions can decrease plant diversity in tropical forests, but that this response may vary with rate of N addition.     

Nitrogen aboveground turnover and soil stocks to 8 m depth in primary and selectively logged forest in southern Amazonia

Extensive areas of Amazonia undergo selective logging, modifying forest structure and nutrient cycles. Anthropogenic‐accelerated rates of nitrogen (N) turnover could increase N loss and affect regeneration, carbon sequestration and timber production. We quantified leaf area reduction, canopy opening and downed biomass and resultant N flux from reduced impact logging (RIL) activities. We compared canopy reduction, surface soil moisture and nitrate to 8 m depth between logged gaps and intact primary forest to determine if logging activities increase subsoil nitrate. To test long‐term logging effects, we evaluated surface N stocks along a 12‐year postlogging chronosequence. At the harvest rate of 2.6 trees ha^?1, total N additions in logging gaps, including leaves and wood from felled crowns (24.8 kg N ha^?1) and other killed trees (41.9 kg N ha^?1), accounted for over 80% of the total N addition to aboveground necromass from all logging activities (81.9 kg N ha^?1). Despite this N turnover by logging, belowground nitrate storage to 8 m depth did not differ between logging gaps and primary forest at the low harvest rate and disturbance intensity of this study. Soil water depletion also did not differ between gaps and primary forest over 1 year, indicating the impact on belowground inorganic N was low. Compared with primary forest, nitrate concentrations to 8 m depth in logging gaps were only significantly higher at 60–100 cm, suggesting some N redistribution beyond the bulk of the fine roots in logging gaps. Extrapolated to the Amazon Basin scale, we provide a conservative estimate that logging damage and bole export under RIL would turn over 0.14 ± 0.07 to 0.23 ± 0.12 Tg N yr^?1 based on 1999–2002 selective logging rates. Greater damage during conventional selective logging would cause higher N turnover throughout the Amazon Basin than our results based on RIL.     

Partitioning direct and indirect human-induced effects on carbon sequestration of managed coniferous forests using model simulations and forest inventories

Temperate forest ecosystems have recently been identified as an important net sink in the global carbon budget. The factors responsible for the strength of the sinks and their permanence, however, are less evident. In this paper, we quantify the present carbon sequestration in Thuringian managed coniferous forests. We quantify the effects of indirect human‐induced environmental changes (increasing temperature, increasing atmospheric CO₂ concentration and nitrogen fertilization), during the last century using BIOME‐BGC, as well as the legacy effect of the current age‐class distribution (forest inventories and BIOME‐BGC). We focused on coniferous forests because these forests represent a large area of central European forests and detailed forest inventories were available. The model indicates that environmental changes induced an increase in biomass C accumulation for all age classes during the last 20 years (1982–2001). Young and old stands had the highest changes in the biomass C accumulation during this period. During the last century mature stands (older than 80 years) turned from being almost carbon neutral to carbon sinks. In high elevations nitrogen deposition explained most of the increase of net ecosystem production (NEP) of forests. CO₂ fertilization was the main factor increasing NEP of forests in the middle and low elevations. According to the model, at present, total biomass C accumulation in coniferous forests of Thuringia was estimated at 1.51 t C ha^?1 yr^?1 with an averaged annual NEP of 1.42 t C ha^?1 yr^?1 and total net biome production of 1.03 t C ha^?1 yr^?1 (accounting for harvest). The annual averaged biomass carbon balance (BCB: biomass accumulation rate‐harvest) was 1.12 t C ha^?1 yr^?1 (not including soil respiration), and was close to BCB from forest inventories (1.15 t C ha^?1 yr^?1). Indirect human impact resulted in 33% increase in modeled biomass carbon accumulation in coniferous forests in Thuringia during the last century. From the forest inventory data we estimated the legacy effect of the age‐class distribution to account for 17% of the inventory‐based sink. Isolating the environmental change effects showed that these effects can be large in a long‐term, managed conifer forest.     

Climate- and crop-responsive emission factors significantly alter estimates of current and future nitrous oxide emissions from fertilizer use

The current Intergovernmental Panel on Climate Change (IPCC) default methodology (tier 1) for calculating nitrous oxide (N₂O) emissions from nitrogen applied to agricultural soils takes no account of either crop type or climatic conditions. As a result, the methodology omits factors that are crucial in determining current emissions, and has no mechanism to assess the potential impact of future climate and land‐use change. Scotland is used as a case study to illustrate the development of a new methodology, which retains the simple structure of the IPCC tier 1 methodology, but incorporates crop‐ and climate‐dependent emission factors (EFs). It also includes a factor to account for the effect of soil compaction because of trampling by grazing animals. These factors are based on recent field studies in Scotland and elsewhere in the UK. Under current conditions, the new methodology produces significantly higher estimates of annual N₂O emissions than the IPCC default methodology, almost entirely because of the increased contribution of grazed pasture. Total emissions from applied fertilizer and N deposited by grazing animals are estimated at 10 662 t N₂O‐N yr^?1 using the newly derived EFs, as opposed to 6 796 t N₂O‐N yr^?1 using the IPCC default EFs. On a spatial basis, emission levels are closer to those calculated using field observations and detailed soil modelling than to estimates made using the IPCC default methodology. This can be illustrated by parts of the western Ayrshire basin, which have previously been calculated to emit 8–9 kg N₂O‐N ha^?1 yr^?1 and are estimated here as 6.25–8.75 kg N₂O‐N ha^?1 yr^?1, while the IPCC default methodology gives a maximum emission level of only 3.75 kg N₂O‐N ha^?1 yr^?1 for the whole area. The new methodology is also applied in conjunction with scenarios for future climate‐ and land‐use patterns, to assess how these emissions may change in the future. The results suggest that by 2080, Scottish N₂O emissions may increase by up to 14%, depending on the climate scenario, if fertilizer and land management practices remain unchanged. Reductions in agricultural land use, however, have the potential to mitigate these increases and, depending on the replacement land use, may even reduce emissions to below current levels.     

Comparing annual and perennial crops for bioenergy production – influence on nitrate leaching and energy balance

Production of energy crops is promoted as a means to mitigate global warming by decreasing dependency on fossil energy. However, agricultural production of bioenergy can have various environmental effects depending on the crop and production system. In a field trial initiated in 2008, nitrate concentration in soil water was measured below winter wheat, grass‐clover and willow during three growing seasons. Crop water balances were modelled to estimate the amount of nitrate leached per hectare. In addition, dry matter yields and nitrogen (N) yields were measured, and N balances and energy balances were calculated. In willow, nitrate concentrations were up to approximately 20 mg l^?1 nitrate‐N during the establishment year, but declined subsequently to <5 mg l^?1 nitrate‐N, resulting in an annual N leaching loss of 18, 3 and 0.3 kg ha^?1 yr^?1 N in the first 3 years after planting. A similar trend was observed in grass‐clover where concentrations stabilized at 2–4 mg l^?1 nitrate‐N from the beginning of the second growing season, corresponding to leaching of approximately 5 kg ha^?1 yr^?1 N. In winter wheat, an annual N leaching loss of 36–68 kg ha^?1 yr^?1 was observed. For comparison, nitrate leaching was also measured in an old willow crop established in 1996 from which N leaching ranged from 6 to 27 kg ha^?1 yr^?1. Dry matter yields ranged between 5.9 and 14.8 Mg yr^?1 with lowest yield in the newly established willow and the highest yield harvested in grass‐clover. Grass‐clover gave the highest net energy yield of 244 GJ ha^?1 yr^?1, whereas old willow, winter wheat and first rotation willow gave net energy yields of 235, 180 and 105 GJ ha^?1 yr^?1. The study showed that perennial crops can provide high energy yields and significantly reduce N losses compared to annual crops.     

Regional gains and losses of nitrogen in the Amazon basin

In order to better understand the relative importance of different ecosystems and nitrogen cycling processes within the Amazon basin to the nitrogen economy of this region, we constructed a generalized nitrogen budget for the region based on data for hydrologic losses of nitrogen and nitrogen fixation in Amazon forests. Data included information available for nitrogen in water entering and leaving both the entire basin and watersheds on oxisol and ultisol soils near Manaus, Brazil, in addition to biological nitrogen fixation in forests on ultisol, oxisol and entisol (‘varzea’) soils in Central Amazonia. Available data indicate that 4–6 kg N ha^?1 yr^?1 are lost via the River Amazonas, and that a similar amount enters in rainfall. Root-associated biological nitrogen fixation contributesca. 2 kg N ha^?1 yr^?1 to forests on oxisols, 20 kg N ha^?1 yr^?1 to forests on utisols, and 200 kg N ha^?1 yr^?1 to forests on fertile varzea soils. There is 5–10 fold more NH₄ ⁺?N than NO₃?N in rain and stream water entering and leaving the waterbasin near Manaus. Calculations based on these data plus certain assumption yield the following regional nitrogen balance estimate: inputs through bulk deposition of 36×10⁸ kg N yr^?1 and through biological nitrogen fixation of 120×10⁸ kg N yr^?1, and outputsvia the River Amazonas of 36×10⁸ kg N yr^?1 andvia denitrification and volatization (by difference) of 120×10⁸ kg N yr^?1.     

The dynamics of soil redistribution and the implications for soil organic carbon accounting in agricultural south‐eastern Australia

Anthropogenically induced change in soil redistribution plays an important role in the soil organic carbon (SOC) budget. Uncertainty of its impact is large because of the dearth of recent soil redistribution estimates concomitant with changing land use and management practices. An Australian national survey used the artificial radionuclide caesium‐137 (¹³⁷Cs) to estimate net (1950s–1990) soil redistribution. South‐eastern Australia showed a median net soil loss of 9.7 t ha^?1 yr^?1. We resurveyed the region using the same ¹³⁷Cs technique and found a median net (1990–2010) soil gain of 3.9 t ha^?1 yr^?1 with an interquartile range from ?1.6 t ha^?1 yr^?1 to +10.7 t ha^?1 yr^?1. Despite this variation, soil erosion across the region has declined as a likely consequence of the widespread adoption of soil conservation measures over the last ca 30 years. The implication of omitted soil redistribution dynamics in SOC accounting is to increase uncertainty and diminish its accuracy.     

Simulated long‐term effects of harvest and biomass residue removal on soil carbon and nitrogen content and productivity for two Upper Great Lakes forest ecosystems

We used the ecosystem process model Biome‐BGC to simulate the effects of harvest and residue removal management scenarios on soil carbon (C), available soil nitrogen (N), net primary production (NPP), and net ecosystem production (NEP) in jack pine (Pinus banksiana Lamb.) and sugar maple (Acer saccharum Marsh) ecosystems in northern Wisconsin, USA. To assess harvest effects, we simulated short (50‐year) and long (100‐year) harvest intervals, high (clear‐cut) and low (selective) harvest intensities, and three levels of residue retention (15%, 25%, and 35%) over a 500‐year period. The model simulation of NPP, soil C accumulation, and NEP agreed reasonably well with biometric and eddy‐covariance measurements of these two ecosystems. The more intensive (50‐year rotation clear‐cuts with low residue retention) harvest scenarios tended to have the greatest NEP (420 and 678 t C ha^?1 for the 500‐year interval for jack pine and sugar maple, respectively). All the harvest scenarios decreased mineral soil C and available mineral soil N content relative to the no‐harvest scenario for jack pine and sugar maple. The rate of change in mineral soil C decreased the greatest in the most intensive biomass removal scenarios (?0.012 and ?0.072 t C ha^?1 yr^?1 relative to no‐harvest for jack pine and sugar maple, respectively) and the smallest decrease was observed in the least intensive biomass removal scenarios (?0.002 and ?0.009 t C ha^?1 yr^?1 relative to no‐harvest for jack pine and sugar maple, respectively). The more intensive biomass removal harvest scenarios in sugar maple significantly decreased peak productivity (NPP) in the simulation period.     

Nitrogen Addition Shapes Soil Phosphorus Availability in Two Reforested Tropical Forests in Southern China

Scant information is available on how soil phosphorus (P) availability responds to atmospheric nitrogen (N) deposition, especially in the tropical zones. This study examined the effect of N addition on soil P availability, and compared this effect between forest sites of contrasting land‐use history. Effects of N addition on soil properties, litterfall production, P release from decomposing litter, and soil P availability were studied in a disturbed (reforested pine forest with previous understory vegetation and litter harvesting) and a rehabilitated (reforested mixed pine/broadleaf forest with no understory vegetation and litter harvesting) tropical forest in southern China. Experimental N‐treatments (above ambient) were the following: Control (no N addition), N50 (50 kg N ha^?1 yr^?1), and N100 (100 kg N ha^?1 yr^?1). Results indicated that N addition significantly decreased soil P availability in the disturbed forest. In the rehabilitated forest, however, soil P availability was significantly increased by N addition. Decreases in soil P availability may be correlated with decreases in rates of P release from decomposing litter in the N‐treated plots, whereas the increase in soil P availability was correlated with an increase in litterfall production. Our results suggest that response of soil P availability to N deposition in the reforested tropical forests in southern China may vary greatly with temporal changes in tree species composition and soil nutrient status, caused by different land‐use practices.     

Interplay between yield,nitrogen application,and logistics on the potential energetic and greenhouse gas emissions from biomass crops

The interplay between nitrogen fertilization (N), yield, nitrous oxide emissions (N₂O), and diesel fuel utilization associated with harvest and transport logistics of biomass crops remains poorly understood. In this research, we show that intensification (in terms of N) of bioenergy cropping to maximize yield supports not only minimized land use but also maximized logistics efficiency in terms of diesel use. This paradigm was examined within the scope of the billion‐ton biofuels vision and the Energy Independence and Security Act of 2007 using potential yields on marginal and prime agricultural land. Sixteen scenarios were investigated that considered the primary factors with agriculture bioenergy; biomass yield (11.2 and 22.4 Mg ha^?1 yr^?1), two nitrogen fertilizer application rates (50 and 100 kg N ha^?1 yr^?1), two Greenhouse Gas Emissions (GHGE) factors for synthetic nitrogen to nitrous oxide (1.5 and 5%), and three harvest/transportation efficiencies (50, 65, and 80%). These scenarios resulted in energy consumption between 747 and 1351 MJ Mg^?1 and GHGE between 72 and 311 kg CO₂ eq Mg^?1. GHGE emissions are strongly related to the emission of nitrous oxide from soils due to nitrogen fertilization and could represent over 80% of the GHGE relative to biomass harvest logistics. These data imply that synthetic N supplementation to maximize yield could reduce the burden due to diesel fuel for harvest, but would rapidly become the most significant contributor to GHGE. Minimizing the impact of N fertilization will be critical for reducing the GHGE associated with biomass production.     

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}.     

Slow response of soil organic matter to the reduction in atmospheric nitrogen deposition in a Norway spruce forest

Global nitrogen (N) deposition rates in terrestrial environments have quadrupled since preindustrial times, causing structural and functional changes of ecosystems. Different emission reduction policies were therefore devised. The aim of our study was to investigate if, and over what timescale, processes of soil organic matter (OM) transformation respond to a decline in atmospheric N deposition. A N‐saturated spruce forest (current N deposition: 34 kg ha^?1 yr^?1; critical N load: 14 kg ha^?1 yr^?1), where N deposition has been reduced to 11.5 kg ha^?1 yr^?1 since 1991, was studied. Besides organic C and organic and inorganic N, noncellulosic carbohydrates, amino sugars and amino acids were determined. A decline in organic N in litter indicated initial effects at plant level. However, there were no changes in biomarkers upon the reduction in N deposition. In addition, inorganic N was not affected by reduced N deposition. The results showed that OM cycling and transformation processes have not responded so far. It was concluded that no direct N deposition effects have occurred due to the large amount of stored organic N, which seems to compensate for the reduction in deposited N. Obviously, the time span of atmospheric N reduction (about 14.5 years) is too short compared with the mean turnover time of litter to cause indirect effects on the composition of organic C and N compounds. It is assumed that ecological processes, such as microbial decomposition or recycling of organic N and C, react slowly, but may start within the next decade with the incorporation of the new litter.     

Nitrogen cycling in coffee plantations

Nitrogen inputs to the coffee ecosystem are dominated by additions of fertilizer-N (100–300 kg N ha^?1 yr^?1). Small nitrogen inputs from rains and variable from inputs fixation by the leguminous shade trees can amount to 1–40 kg N ha^?1 yr^?1. Organic matter mineralization can be an important nitrogen source also. Nitrogen losses from the system include removal of N in the harvest (15–90 kg N ha^?1 yr^?1), the removal of coffee and shade tree prunings for firewood, losses from erosion, leaching losses and gaseous losses. Unfortunately, very little information exists for leaching and gaseous losses and for the factors that regulate these processes. The overall nitrogen cycle in shaded coffee plantings includes three interrelated subsystems. These are the coffee, shade and weeds subcycles.     

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.     

Nitrogen fixation and nitrogen balance studies in Rhizobium-VA mycorrhiza inoculated legume-grass association by15N isotope dilution technique under a field condition

A mixed pasture comprising of buffel grass and a legume siratro was studied under field condition for a two-year period to know the fodder yield increase, nitrogen fixation and nitrogen balance with and without the inoculation of VA mycorrhiza to grass and Rhizobium to legume component.¹⁵N dilution technique was followed using labelled ammonium sulphate. The data showed that during the first year of the above study combined inoculation of VA mycorrhiza and Rhizobium to grass and legume respectively significantly increased the total dry matter (DM) (23,900 kg ha^–1 yr^–1) and total N content (308 kg ha^–1 yr^–1) of the mixed pasture over the uninoculated mixture. However, the above increase due to combined inoculation was maximum during second year with respect to DM yield (28,200 kg ha^–1 yr^–1), but the total N harvested through grass-legume mixture was comparatively lower than the first year (297 kg ha^–1 yr^–1). The amount of biologically fixed N was highest in the first year (79 kg ha^–1 yr^–1) and showed a very drastic reduction at the end of second year (39 kg ha^–1 yr^–1). A positive nitrogen balance was observed in the grass-legume mixture irrespective of inoculation of VA mycorrhiza and/or Rhizobium.     

Conversion from forests to pastures in the Colombian Amazon leads to contrasting soil carbon dynamics depending on land management practices

Strategies to mitigate climate change by reducing deforestation and forest degradation (e.g. REDD+) require country‐ or region‐specific information on temporal changes in forest carbon (C) pools to develop accurate emission factors. The soil C pool is one of the most important C reservoirs, but is rarely included in national forest reference emission levels due to a lack of data. Here, we present the soil organic C (SOC) dynamics along 20 years of forest‐to‐pasture conversion in two subregions with different management practices during pasture establishment in the Colombian Amazon: high‐grazing intensity (HG) and low‐grazing intensity (LG) subregions. We determined the pattern of SOC change resulting from the conversion from forest (C3 plants) to pasture (C4 plants) by analysing total SOC stocks and the natural abundance of the stable isotopes ¹³C along two 20‐year chronosequences identified in each subregion. We also analysed soil N stocks and the natural abundance of ¹⁵N during pasture establishment. In general, total SOC stocks at 30 cm depth in the forest were similar for both subregions, with an average of 47.1 ± 1.8 Mg C ha^?1 in HG and 48.7 ± 3.1 Mg C ha^?1 in LG. However, 20 years after forest‐to‐pasture conversion SOC in HG decreased by 20%, whereas in LG SOC increased by 41%. This net SOC decrease in HG was due to a larger reduction in C3‐derived input and to a comparatively smaller increase in C4‐derived C input. In LG both C3‐ and C4‐derived C input increased along the chronosequence. N stocks were generally similar in both subregions and soil N stock changes during pasture establishment were correlated with SOC changes. These results emphasize the importance of management practices involving low‐grazing intensity in cattle activities to preserve SOC stocks and to reduce C emissions after land‐cover change from forest to pasture in the Colombian Amazon.     

Bryophytes attenuate anthropogenic nitrogen inputs in boreal forests

Productivity in boreal ecosystems is primarily limited by available soil nitrogen (N), and there is substantial interest in understanding whether deposition of anthropogenically derived reactive nitrogen (N_r) results in greater N availability to woody vegetation, which could result in greater carbon (C) sequestration. One factor that may limit the acquisition of N_r by woody plants is the presence of bryophytes, which are a significant C and N pool, and a location where associative cyanobacterial N‐fixation occurs. Using a replicated stand‐scale N‐addition experiment (five levels: 0, 3, 6, 12, and 50 kg N ha^?1 yr^?1; n=6) in the boreal zone of northern Sweden, we tested the hypothesis that sequestration of N_r into bryophyte tissues, and downregulation of N‐fixation would attenuate N_r inputs, and thereby limit anthropogenic N_r acquisition by woody plants. Our data showed that N‐fixation per unit moss mass and per unit area sharply decreased with increasing N addition. Additionally, the tissue N concentrations of Pleuorzium schreberi increased and its biomass decreased with increasing N addition. This response to increasing N addition caused the P. schreberi N pool to be stable at all but the highest N addition rate, where it significantly decreased. The combined effects of changed N‐fixation and P. schreberi biomass N accounted for 56.7% of cumulative N_r additions at the lowest N_r addition rate, but only a minor fraction for all other treatments. This ‘bryophyte effect’ can in part explain why soil inorganic N availability and acquisition by woody plants (indicated by their δ¹⁵N signatures) remained unchanged up to N addition rates of 12 kg ha^?1 yr^?1 or greater. Finally, we demonstrate that approximately 71.8% of the boreal forest experiences N_r deposition rates at or below 3 kg ha^?1 yr^?1, suggesting that bryophytes likely limit woody plant acquisition of ambient anthropogenic N_r inputs throughout a majority of the boreal forest.