Enhanced CO2 uptake is marginally offset by altered fluxes of non-CO2 greenhouse gases in global forests and grasslands under N deposition

Despite the increasing impact of atmospheric nitrogen (N) deposition on terrestrial greenhouse gas (GHG) budget, through driving both the net atmospheric CO₂ exchange and the emission or uptake of non-CO₂ GHGs (CH₄ and N₂O), few studies have assessed the climatic impact of forests and grasslands under N deposition globally based on different bottom-up approaches. Here, we quantify the effects of N deposition on biomass C increment, soil organic C (SOC), CH₄ and N₂O fluxes and, ultimately, the net ecosystem GHG balance of forests and grasslands using a global comprehensive dataset. We showed that N addition significantly increased plant C uptake (net primary production) in forests and grasslands, to a larger extent for the aboveground C (aboveground net primary production), whereas it only caused a small or insignificant enhancement of SOC pool in both upland systems. Nitrogen addition had no significant effect on soil heterotrophic respiration (R_H) in both forests and grasslands, while a significant N-induced increase in soil CO₂ fluxes (R_S, soil respiration) was observed in grasslands. Nitrogen addition significantly stimulated soil N₂O fluxes in forests (76%), to a larger extent in grasslands (87%), but showed a consistent trend to decrease soil uptake of CH₄, suggesting a declined sink capacity of forests and grasslands for atmospheric CH₄ under N enrichment. Overall, the net GHG balance estimated by the net ecosystem production-based method (forest, 1.28 Pg CO₂-eq year⁻¹ vs. grassland, 0.58 Pg CO₂-eq year⁻¹) was greater than those estimated using the SOC-based method (forest, 0.32 Pg CO₂-eq year⁻¹ vs. grassland, 0.18 Pg CO₂-eq year⁻¹) caused by N addition. Our findings revealed that the enhanced soil C sequestration by N addition in global forests and grasslands could be only marginally offset (1.5%–4.8%) by the combined effects of its stimulation of N₂O emissions together with the reduced soil uptake of CH₄.     

Climatic role of terrestrial ecosystem under elevated CO2: a bottom‐up greenhouse gases budget

The net balance of greenhouse gas (GHG) exchanges between terrestrial ecosystems and the atmosphere under elevated atmospheric carbon dioxide (CO₂) remains poorly understood. Here, we synthesise 1655 measurements from 169 published studies to assess GHGs budget of terrestrial ecosystems under elevated CO₂. We show that elevated CO₂ significantly stimulates plant C pool (NPP) by 20%, soil CO₂ fluxes by 24%, and methane (CH₄) fluxes by 34% from rice paddies and by 12% from natural wetlands, while it slightly decreases CH₄ uptake of upland soils by 3.8%. Elevated CO₂ causes insignificant increases in soil nitrous oxide (N₂O) fluxes (4.6%), soil organic C (4.3%) and N (3.6%) pools. The elevated CO₂‐induced increase in GHG emissions may decline with CO₂ enrichment levels. An elevated CO₂‐induced rise in soil CH₄ and N₂O emissions (2.76 Pg CO₂‐equivalent year^?1) could negate soil C enrichment (2.42 Pg CO₂ year^?1) or reduce mitigation potential of terrestrial net ecosystem production by as much as 69% (NEP, 3.99 Pg CO₂ year^?1) under elevated CO₂. Our analysis highlights that the capacity of terrestrial ecosystems to act as a sink to slow climate warming under elevated CO₂ might have been largely offset by its induced increases in soil GHGs source strength.     

Carbon Abatement and Emissions Associated with the Gasification of Walnut Shells for Bioenergy and Biochar Production

By converting biomass residue to biochar, we could generate power cleanly and sequester carbon resulting in overall greenhouse gas emissions (GHG) savings when compared to typical fossil fuel usage and waste disposal. We estimated the carbon dioxide (CO₂) abatements and emissions associated to the concurrent production of bioenergy and biochar through biomass gasification in an organic walnut farm and processing facility in California, USA. We accounted for (i) avoided-CO₂ emissions from displaced grid electricity by bioenergy; (ii) CO₂ emissions from farm machinery used for soil amendment of biochar; (iii) CO₂ sequestered in the soil through stable biochar-C; and (iv) direct CO₂ and nitrous oxide (N₂O) emissions from soil. The objective of these assessments was to pinpoint where the largest C offsets can be expected in the bioenergy-biochar chain. We found that energy production from gasification resulted in 91.8% of total C offsets, followed by stable biochar-C (8.2% of total C sinks), offsetting a total of 107.7 kg CO₂-C eq Mg^-1 feedstock. At the field scale, we monitored gas fluxes from soils for 29 months (180 individual observations) following field management and precipitation events in addition to weekly measurements within three growing seasons and two tree dormancy periods. We compared four treatments: control, biochar, compost, and biochar combined with compost. Biochar alone or in combination with compost did not alter total N₂O and CO₂ emissions from soils, indicating that under the conditions of this study, biochar-prompted C offsets may not be expected from the mitigation of direct soil GHG emissions. However, this study revealed a case where a large environmental benefit was given by the waste-to-bioenergy treatment, addressing farm level challenges such as waste management, renewable energy generation, and C sequestration.     

Nitrogen deposition promotes ecosystem carbon accumulation by reducing soil carbon emission in a subtropical forest

Background and aims

Tropical and subtropical forests are experiencing high levels of atmospheric nitrogen (N) deposition, but the responses of such forests ecosystems to N deposition remain poorly understood.

Methods

We conducted an 8-year field experiment examining the effect of experimental N deposition on plant growth, soil carbon dioxide efflux, and net ecosystem production (NEP) in a subtropical Chinese fir forest. The quantities of N added were 0 (control), 60, 120, and 240 kg ha^?1 year^?1.

Results

NEP was lowest under ambient conditions and highest with 240 kg of N ha^?1 year^?1 treatment. The net increase in ecosystem carbon (C) storage ranged from 9.2 to 16.4 kg C per kg N added in comparison with control. In addition, N deposition treatments significantly decreased heterotrophic respiration (by 0.69–1.85 t C ha^?1 year^?1) and did not affect plant biomass. The nitrogen concentrations were higher in needles than that in fine roots.

Conclusions

Our findings suggest that the young Chinese fir forest is carbon source and N deposition would sequester additional atmospheric CO₂ at high levels N input, mainly due to reduced soil CO₂ emission rather than increased plant growth, and the amount of sequestered C depended on the rate of N deposition.     

Global warming intensity of biofuel derived from switchgrass grown on marginal land in Michigan

Energy crops for biofuel production, especially switchgrass (Panicum virgatum), are of interest from a climate change perspective. Here, we use outputs from a crop growth model and life cycle assessment (LCA) to examine the global warming intensity (GWI; g CO₂ MJ⁻¹) and greenhouse gas (GHG) mitigation potential (Mg CO₂ year⁻¹) of biofuel systems based on a spatially explicit analysis of switchgrass grown on marginal land (abandoned former cropland) in Michigan, USA. We find that marginal lands in Michigan can annually produce over 0.57 hm³ of liquid biofuel derived from nitrogen-fertilized switchgrass, mitigating 1.2–1.5 Tg of CO₂ year⁻¹. About 96% of these biofuels can meet the Renewable Fuel Standard (60% reduction in lifecycle GHG emissions compared with conventional gasoline; GWI ≤37.2 g CO₂ MJ⁻¹). Furthermore, 73%–75% of these biofuels are carbon-negative (GWI less than zero) due to enhanced soil organic carbon (SOC) sequestration. However, simulations indicate that SOC levels would fail to increase and even decrease on the 11% of lands where SOC stocks >>200 Mg C ha⁻¹, leading to carbon intensities greater than gasoline. Results highlight the strong climate mitigation potential of switchgrass grown on marginal lands as well as the needs to avoid carbon rich soils such as histosols and wetlands and to ensure that productivity will be sufficient to provide net mitigation.     

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.     

Amazonia and the modern carbon cycle: lessons learned

In this paper, we review some critical issues regarding carbon cycling in Amazonia, as revealed by several studies conducted in the Large Scale Biosphere Atmosphere Experiment in Amazonia (LBA). We evaluate both the contribution of this magnificent biome for the global net primary productivity/net ecosystem exchange (NPP/NEE) and the feedbacks of climate change on the dynamics of Amazonia. In order to place Amazonia in a global perspective and make the carbon flux obtained through the LBA project comparable with global carbon budgets, we extrapolated NPP/NEE values found by LBA studies to the entire area of the Brazilian Amazon covered by rainforest. The carbon emissions due to land use changes for the tropical regions of the world produced values from 0.96 to 2.4 Pg C year⁻¹, while atmospheric CO₂ inversion models have recently indicated that tropical lands in the Americas could be exchanging a net 0.62±1.15 Pg C year⁻¹ with the atmosphere. The difference calculated from these two methods would imply a local sink of approximately 1.6–1.7 Pg C year⁻¹, or a source of 0.85 ton C ha⁻¹ year⁻¹. Using our crude extrapolation of LBA values for the Amazon forests (5 million km²) we estimate a range for the C flux in the region of −3.0 to 0.75 Pg C year⁻¹. The exercise here does not account for environmental variability across the region, but it is an important driver for present and future studies linking local process (i.e. nutrient availability, photosynthetic capacity, and so forth) to global and regional dynamic approaches.     

Proteomics reveals the adaptability mechanism of Brassica napus to short-term boron deprivation

The application of pyrogenic carbon, biochar, to agricultural soils is currently discussed as a win-win strategy to sequester carbon in soil, thus improving soil fertility and mitigate global warming. Our aim was to investigate if biochar may improve plant eco-physiological responses under sufficient water supply as well as moderate drought stress. A fully randomized greenhouse study was conducted with the pseudo-cereal Chenopodium quinoa Willd, using three levels of biochar addition (0, 100 and 200?t ha^?1) to a sandy soil and two water treatments (60% and 20% of the water holding capacity of the control), investigating growth, water use efficiency, eco-physiological parameters and greenhouse gas (GHG) fluxes. Biochar application increased growth, drought tolerance and leaf-N- and water-use efficiency of quinoa despite larger plant?Cleaf areas. The plants growing in biochar-amended soil accumulated exactly the same amount of nitrogen in their larger leaf biomass than the control plants, causing significantly decreased leaf N-, proline- and chlorophyll-concentrations. In this regard, plant responses to biochar closely resembled those to elevated CO₂. However, neither soil- nor plant?Csoil-respiration was higher in the larger plants, indicating less respiratory C losses per unit of biomass produced. Soil-N₂O emissions were significantly reduced with biochar. The large application rate of 200?t ha^?1 biochar did not improve plant growth compared to 100?t ha^?1; hence an upper beneficial level exists. For quinoa grown in a sandy soil, biochar application might hence provide a win-win strategy for increased crop production, GHG emission mitigation and soil C sequestration.     

An appraisal of the utility of biochar in a rotation involving tobacco–rice in southern China

The employment of biochar in crop production can not only improve soil quality, but also helps the field ecosystem to fix carbon and reduce emissions. Although the benefits of their application in crop production have been more and more confirmed, it is not clear when it comes to the acidic soil of tobacco and rice rotation. A tobacco–rice rotation experiment was conducted in southern China to probe the application value of biochar under these conditions. Three biochar application rates were employed in this experiment. BC0 (without biochar), BC25 (25 t ha⁻¹), and BC50 (50 t ha⁻¹). The findings show that biochar significantly boosted soil fertility and crop yields. Meanwhile, the soil organic carbon of tobacco rice rotation field with biochar increased by 31.76%. After a whole growth period of tobacco and rice, the cumulative emission reduction of CO₂ and N₂O from the soil by biochar were 15,944 kg ha⁻¹ and 1810 g ha⁻¹, respectively. The use of biochar not only significantly improved the bacterial diversity of tobacco and rice rotation soil, but also altered the original microbial community structure. The profusion of Proteobacteria and Acidobacteria was reduced and the abundance of Actinobacteria and Bacteroidetes was enhanced in the treatments with biochar. Among them, Sphingomonadales, Planctomycotes, and Ktedonobacteria, which are beneficial to plant growth and soil health, have become key phylotypes. The carbon balance analysis data show that the net carbon sequestration of the two treatments with biochar is positive, while that of the treatment without biochar is negative. In terms of economic benefit, the application of biochar increased the average of 2.055 CNY kg⁻¹ consumed energy (CE) in the whole tobacco–rice rotation system. The ecological benefit was 0.51 kg C kg⁻¹ CE. In conclusion, biochar can be effectively used in the practice of tobacco–rice rotation and acidic soil improvement in southern China.     

Carbon footprint of rice production under biochar amendment – a case study in a Chinese rice cropping system

As a controversial strategy to mitigate global warming, biochar application into soil highlights the need for life cycle assessment before large‐scale practice. This study focused on the effect of biochar on carbon footprint of rice production. A field experiment was performed with three treatments: no residue amendment (Control), 6 t ha^?1 yr^?1 corn straw (CS) amendment, and 2.4 t ha^?1 yr^?1 corn straw‐derived biochar amendment (CBC). Carbon footprint was calculated by considering carbon source processes (pyrolysis energy cost, fertilizer and pesticide input, farmwork, and soil greenhouse gas emissions) and carbon sink processes (soil carbon increment and energy offset from pyrolytic gas). On average over three consecutive rice‐growing cycles from year 2011 to 2013, the CS treatment had a much higher carbon intensity of rice (0.68 kg CO₂‐C equivalent (CO₂‐C_e) kg^?1 grain) than that of Control (0.24 kg CO₂‐C_e kg^?1 grain), resulting from large soil CH₄ emissions. Biochar amendment significantly increased soil carbon pool and showed no significant effect on soil total N₂O and CH₄ emissions relative to Control; however, due to a variation in net electric energy input of biochar production based on different pyrolysis settings, carbon intensity of rice under CBC treatment ranged from 0.04 to 0.44 kg CO₂‐C_e kg^?1 grain. The results indicated that biochar strategy had the potential to significantly reduce the carbon footprint of crop production, but the energy‐efficient pyrolysis technique does matter.     

Priming effect stimulates carbon release from thawed permafrost

Climate warming leads to widespread permafrost thaw with a fraction of the thawed permafrost carbon (C) being released as carbon dioxide (CO₂), thus triggering a positive permafrost C-climate feedback. However, large uncertainty exists in the size of this model-projected feedback, partly owing to the limited understanding of permafrost CO₂ release through the priming effect (i.e., the stimulation of soil organic matter decomposition by external C inputs) upon thaw. By combining permafrost sampling from 24 sites on the Tibetan Plateau and laboratory incubation, we detected an overall positive priming effect (an increase in soil C decomposition by up to 31%) upon permafrost thaw, which increased with permafrost C density (C storage per area). We then assessed the magnitude of thawed permafrost C under future climate scenarios by coupling increases in active layer thickness over half a century with spatial and vertical distributions of soil C density. The thawed C stocks in the top 3 m of soils from the present (2000–2015) to the future period (2061–2080) were estimated at 1.0 (95% confidence interval (CI): 0.8–1.2) and 1.3 (95% CI: 1.0–1.7) Pg (1 Pg = 10¹⁵ g) C under moderate and high Representative Concentration Pathway (RCP) scenarios 4.5 and 8.5, respectively. We further predicted permafrost priming effect potential (priming intensity under optimal conditions) based on the thawed C and the empirical relationship between the priming effect and permafrost C density. By the period 2061–2080, the regional priming potentials could be 8.8 (95% CI: 7.4–10.2) and 10.0 (95% CI: 8.3–11.6) Tg (1 Tg = 10¹² g) C year⁻¹ under the RCP 4.5 and RCP 8.5 scenarios, respectively. This large CO₂ emission potential induced by the priming effect highlights the complex permafrost C dynamics upon thaw, potentially reinforcing permafrost C-climate feedback.     

Indonesia’s blue carbon: a globally significant and vulnerable sink for seagrass and mangrove carbon

The global significance of carbon storage in Indonesia’s coastal wetlands was assessed based on published and unpublished measurements of the organic carbon content of living seagrass and mangrove biomass and soil pools. For seagrasses, median above- and below-ground biomass was 0.29 and 1.13 Mg C ha^?1 respectively; the median soil pool was 118.1 Mg C ha^?1. Combining plant biomass and soil, median carbon storage in an Indonesian seagrass meadow is 119.5 Mg C ha^?1. Extrapolated to the estimated total seagrass area of 30,000 km², the national storage value is 368.5 Tg C. For mangroves, median above- and below-ground biomass was 159.1 and 16.7 Mg C ha^?1, respectively; the median soil pool was 774.7 Mg C ha^?1. The median carbon storage in an Indonesian mangrove forest is 950.5 Mg C ha^?1. Extrapolated to the total estimated mangrove area of 31,894 km², the national storage value is 3.0 Pg C, a likely underestimate if these habitats sequester carbon at soil depths >1 m and/or sequester inorganic carbon. Together, Indonesia’s seagrasses and mangroves conservatively account for 3.4 Pg C, roughly 17 % of the world’s blue carbon reservoir. Continued degradation and destruction of these wetlands has important consequences for CO₂ emissions and dissolved carbon exchange with adjacent coastal waters. We estimate that roughly 29,040 Gg CO₂ (eq.) is returned annually to the atmosphere–ocean pool. This amount is equivalent to about 3.2 % of Indonesia’s annual emissions associated with forest and peat land conversion. These results highlight the urgent need for blue carbon and REDD+ projects as a means to stem the decline in wetland area and to mitigate the release of a significant fraction of the world’s coastal carbon stores.     

Bioprocess strategies for enhancing biomolecules productivity in Chlorella fusca LEB 111 using CO2 a carbon source

The aim of this study was to evaluate the influence of different carbon dioxide (CO₂) concentrations on the distribution of carbon forms in the culture medium and the biomass production and biomolecules productivity of the strain Chlorella fusca LEB 111. In this study, experiments were carried out in which C. fusca cultures were exposed to different CO₂ concentrations, 0.03% (0.08 ml_CO2 ml_medium⁻¹ days⁻¹), 5% (0.18 ml_CO2 ml_medium⁻¹ days⁻¹), and 15% vol/vol CO₂ (0.54 ml_CO2 ml_medium⁻¹ days⁻¹). Among the carbon chemical species distributions in the culture medium, bicarbonate was predominant (94.2–98.9%), with the highest quantitative percentage in the experiment receiving a 15% CO₂ injection. C. fusca LEB 111 cultivated with 15% CO₂ showed the highest biomass productivity (194.3 mg L⁻¹ days⁻¹) and CO₂ fixation rate (390.9 mg L⁻¹ days⁻¹). The carbohydrate productivity in the culture that received 15% CO₂ was 46.2% higher than the value verified for the culture with the addition of CO₂ from the air (0.03% CO₂). In addition, CO₂ concentration providing increases of 0.03–15% to C. fusca cultures resulted in a 31.6% increase in the lipid productivity. These results showed that C. fusca can be used for CO₂ bioconversion and for producing biomass with potential applications for biofuels and bioproducts.     

Increased CO2 fluxes from a sandy Cambisol under agricultural use in the Wendland region,Northern Germany,three years after biochar substrates application

In recent years, biochar has been discussed as an opportunity for carbon sequestration in arable soils. Field experiments under realistic conditions investigating the CO₂ emission from soil after biochar combined with fertilizer additions are scarce. Therefore, we investigated the CO₂ emission and its ¹³C signature after addition of compost, biogas digestate (originating from C4 feedstock) and mineral fertilizer with and without biochar (0, 3, 10, 40 Mg biochar/ha) to a sandy Cambisol in Northern Germany. Biomass residues were pyrolized at ~650°C to obtain biochar with C3 signature. Gas samples were taken biweekly during the growing season using static chambers three years after biochar substrate addition. The CO₂ concentration and its δ¹³C isotope signature were measured using a gas chromatograph coupled to an isotope ratio mass spectrometer. Results showed increased CO₂ emission (30%–60%) when high biochar amount (40 Mg/ha) was applied three years ago together with mineral fertilizer and biogas digestate. On average, 59% of the emitted CO₂ had a C3 signature (thus, deriving from biochar and/or soil organic matter), independent of the amount of biochar added. In addition, our results clearly demonstrated that only a small amount of released CO₂ derived from biochar. The results of this field experiment suggest that biochar most likely stimulates microbial activity in soil leading to increased CO₂ emissions derived from soil organic matter and fertilizers mineralization rather than from biochar. Nevertheless, compared to the amount of carbon added by biochar, additional CO₂ emission is marginal corroborating the C sequestration potential of biochar.     

Holocene radiative forcing impact of northern peatland carbon accumulation and methane emissions

Throughout the Holocene, northern peatlands have both accumulated carbon and emitted methane. Their impact on climate radiative forcing has been the net of cooling (persistent CO₂ uptake) and warming (persistent CH₄ emission). We evaluated this by developing very simple Holocene peatland carbon flux trajectories, and using these as inputs to a simple atmospheric perturbation model. Flux trajectories are based on estimates of contemporary CH₄ flux (15–50 Tg CH₄ yr⁻¹), total accumulated peat C (250–450 Pg C), and peatland initiation dates. The contemporary perturbations to the atmosphere due to northern peatlands are an increase of ∼100 ppbv CH₄ and a decrease of ∼35 ppmv CO₂. The net radiative forcing impact northern peatlands is currently about −0.2 to −0.5 W m⁻² (a cooling). It is likely that peatlands initially caused a net warming of up to +0.1 W m⁻², but have been causing an increasing net cooling for the past 8000–11 000 years. A series of sensitivity simulations indicate that the current radiative forcing impact is determined primarily by the magnitude of the contemporary methane flux and the magnitude of the total C accumulated as peat, and that radiative forcing dynamics during the Holocene depended on flux trajectory, but the overall pattern was similar in all cases.     

Exposure to an enriched CO2 atmosphere alters carbon assimilation and allocation in a pine forest ecosystem

We linked a leaf-level CO₂ assimilation model with a model that accounts for light attenuation in the canopy and measurements of sap-flux-based canopy conductance into a new canopy conductance-constrained carbon assimilation (4C-A) model. We estimated canopy CO₂ uptake (A_nC) at the Duke Forest free-air CO₂ enrichment (FACE) study. Rates of A_nC estimated from the 4C-A model agreed well with leaf gas exchange measurements (A_net) in both CO₂ treatments. Under ambient conditions, monthly sums of net CO₂ uptake by the canopy (A_nC) were 13% higher than estimates based on eddy-covariance and chamber measurements. Annual estimates of A_nC were only 3% higher than carbon (C) accumulations and losses estimated from ground-based measurements for the entire stand. The C budget for the Pinus taeda component was well constrained (within 1% of ground-based measurements). Although the closure of the C budget for the broadleaf species was poorer (within 20%), these species are a minor component of the forest. Under elevated CO₂, the C used annually for growth, turnover, and respiration balanced only 80% of the A_nC. Of the extra 700 g C m⁻² a⁻¹ (1999 and 2000 average), 86% is attributable to surface soil CO₂ efflux. This suggests that the production and turnover of fine roots was underestimated or that mycorrhizae and rhizodeposition became an increasingly important component of the C balance. Under elevated CO₂, net ecosystem production increased by 272 g C m⁻² a⁻¹: 44% greater than under ambient CO₂. The majority (87%) of this C was sequestered in a moderately long-term C pool in wood, with the remainder in the forest floor–soil subsystem.     

Carbon Sequestration in Fine Roots and Foliage Biomass Offsets Soil CO2 Effluxes along a 19-year Chronosequence of Shrub Willow (Salix x dasyclados) Biomass Crops

Previous greenhouse gas (GHG) assessments for the shrub willow biomass crops (SWBC) production system lacked quantitative data on the soil CO₂ efflux (F_c). This study quantifies the mean annual cumulative F_c, the C sequestration in the above- and belowground biomass, and the carbon balance of the production system. We utilized four SWBC fields, which have been in production for 5, 12, 14, and 19 years. Two treatments were applied: continuous production (CP)—shrub willows were harvested, and stools were allowed to regrow, and tear-out (TO) (crop removal)—shrub willows were harvested, and stools were sprayed with herbicide following spring, crushed, and mixed into the soil. Mean annual cumulative F_c were measured using dynamic closed chambers (LI-8100A and LI-8150). Across different age classes, the mean cumulative F_c ranged from 27.2 to 35.5 Mg CO₂ ha^?1 year^?1 for CP and 26.5 to 29.3 Mg CO₂ ha^?1 year^?1 for TO. The combined carbon (C) sequestration of the standing above- and belowground biomass, excluding stems, ranged from 50.6 to 94.8 Mg CO₂ eqv. ha^?1. In the CP treatment, the annual C sequestration in the fine roots and foliage offsets the annual cumulative F_c. Across different age classes, C balances ranged from ?21.5 to ?59.3 Mg CO₂ ha^?1 for CP and 26.5 to 29.3 Mg CO₂ ha^?1 for TO. The GHG potential of SWBC is about ?36.3 Mg CO₂ eqv. ha^?1 at the end of 19 years, suggesting that the SWBC system sequesters C until termination of the crop.     

Net ecosystem carbon exchange and the greenhouse gas balance of tidal marshes along an estuarine salinity gradient

Tidal wetlands are productive ecosystems with the capacity to sequester large amounts of carbon (C), but we know relatively little about the impact of climate change on wetland C cycling in lower salinity (oligohaline and tidal freshwater) coastal marshes. In this study we assessed plant production, C cycling and sequestration, and microbial organic matter mineralization at tidal freshwater, oligohaline, and salt marsh sites along the salinity gradient in the Delaware River Estuary over four years. We measured aboveground plant biomass, carbon dioxide (CO₂) and methane (CH₄) exchange between the marsh and atmosphere, microbial sulfate reduction and methanogenesis in marsh soils, soil biogeochemistry, and C sequestration with radiodating of soils. A simple model was constructed to estimate monthly and annually integrated rates of gross ecosystem production (GEP), ecosystem respiration (ER) to carbon dioxide ( \( {\text{ER}}_{{{\text{CO}}_{2} }} \) ) or methane ( \( {\text{ER}}_{{{\text{CH}}_{4} }} \) ), net ecosystem production (NEP), the contribution of sulfate reduction and methanogenesis to ER, and the greenhouse gas (GHG) source or sink status of the wetland for 2 years (2007 and 2008). All three marsh types were highly productive but evidenced different patterns of C sequestration and GHG source/sink status. The contribution of sulfate reduction to total ER increased along the salinity gradient from tidal freshwater to salt marsh. The Spartina alterniflora dominated salt marsh was a C sink as indicated by both NEP (~140 g C m^?2 year^?1) and ²¹⁰Pb radiodating (336 g C m^?2 year^?1), a minor sink for atmospheric CH₄, and a GHG sink (~620 g CO_2-eq m^?2 year^?1). The tidal freshwater marsh was a source of CH₄ to the atmosphere (~22 g C–CH₄ m^?2 year^?1). There were large interannual differences in plant production and therefore C and GHG source/sink status at the tidal freshwater marsh, though ²¹⁰Pb radiodating indicated modest C accretion (110 g C m^?2 year^?1). The oligohaline marsh site experienced seasonal saltwater intrusion in the late summer and fall (up to 10 mS cm^?1) and the Zizania aquatica monoculture at this site responded with sharp declines in biomass and GEP in late summer. Salinity intrusion was also linked to large effluxes of CH₄ at the oligohaline site (>80 g C–CH₄ m^?2 year^?1), making this site a significant GHG source (>2,000 g CO_2-eq m^?2 year^?1). The oligohaline site did not accumulate C over the 2 year study period, though ²¹⁰Pb dating indicated long term C accumulation (250 g C m^?2 year^?1), suggesting seasonal salt-water intrusion can significantly alter C cycling and GHG exchange dynamics in tidal marsh ecosystems.     

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.     

Amending biochar affected enzyme activities and nitrogen turnover in Phaeozem and Luvisol

Soil nitrogen (N) is a vital source of nutrients for maintaining soil fertility and crop production. However, the effect of biochar application rate on the mechanism of organic N transformation and the contribution of enzyme mineralization is still unclear. Therefore, we conducted two 5-year field experiments in contrasting soils (Phaeozem and Luvisol) with biochar application rate at 0 t hm⁻² (CK, 0), 22.5 t hm⁻² (D₁, 1%), 67.5 t hm⁻² (D₂, 3%), and 112.5 t hm⁻² (D₃, 5%) to investigate the potential effects of biochar application rate on soil organic nitrogen (N) turnover and its linkage to enzymatic mineralization in contrasting soil. The results showed that soil organic carbon (SOC) and microbial biomass nitrogen (MBN) contents, microbial biomass carbon to nitrogen ratio (MBC:MBN) and protease activity are significantly influenced by biochar application rate whereas not by soil type. Ammonium nitrogen (NH₄⁺-N) and nitrate nitrogen (NO₃⁻-N) contents, and dehydrogenase activity are significantly changed by soil type whereas not by biochar application rate. Based on the redundancy analysis, we found that organic N fractions are associated with MBN, SOC, and protease in Phaeozem, but related to protease activity in Luvisol. Our findings indicate that organic N turnover is not only related to the bioavailability of N but also requires carbon substrates in Phaeozem, whereas the transformation of organic N in Luvisol is dominated by enzymatic mineralization as the relatively low level of bioavailable N.