Increasing riverine export of dissolved organic carbon from China

River transport of dissolved organic carbon (DOC) to the ocean is a crucial but poorly quantified regional carbon cycle component. Large uncertainties remaining on the riverine DOC export from China, as well as its trend and drivers of change, have challenged the reconciliation between atmosphere-based and land-based estimates of China's land carbon sink. Here, we harmonized a large database of riverine in-situ measurements and applied a random forest model, to quantify riverine DOC fluxes (F_DOC) and DOC concentrations (C_DOC) in rivers across China. This study proposes the first DOC modeling effort capable of reproducing well the magnitude of riverine C_DOC and F_DOC, as well as its trends, on a monthly scale and with a much wider spatial distribution over China compared to previous studies that mainly focused on annual-scale estimates and large rivers. Results show that over the period 2001–2015, the average C_DOC was 2.25 ± 0.45 mg/L and average F_DOC was 4.04 ± 1.02 Tg/year. Simultaneously, we found a significant increase in F_DOC (+0.044 Tg/year², p = .01), but little change in C_DOC (−0.001 mg/L/year, p > .10). Although the trend in C_DOC is not significant at the country scale, it is significantly increasing in the Yangtze River Basin and Huaihe River Basin (0.005 and 0.013 mg/L/year, p < .05) while significantly decreasing in the Yellow River Basin and Southwest Rivers Basin (−0.043 and −0.014 mg/L/year, p = .01). Changes in hydrology, play a stronger role than direct impacts of anthropogenic activities in determining the spatio-temporal variability of F_DOC and C_DOC across China. However, and in contrast with other basins, the significant increase in C_DOC in the Yangtze River Basin and Huaihe River Basin is attributable to direct anthropogenic activities. Given the dominance of hydrology in driving F_DOC, the increase in F_DOC is likely to continue under the projected increase in river discharge over China resulting from a future wetter climate.     

Alternative explanations for rising dissolved organic carbon export from organic soils

Since 1988, there has been, on average, a 91% increase in dissolved organic carbon (DOC) concentrations of UK lakes and streams in the Acid Waters Monitoring Network (AWMN). Similar DOC increases have been observed in surface waters across much of Europe and North America. Much of the debate about the causes of rising DOC has, as in other studies relating to the carbon cycle, focused on factors related to climate change. Data from our peat‐core experiments support an influence of climate on DOC, notably an increase in production with temperature under aerobic, and to a lesser extent anaerobic, conditions. However, we argue that climatic factors may not be the dominant drivers of DOC change. DOC solubility is suppressed by high soil water acidity and ionic strength, both of which have decreased as a result of declining sulphur deposition since the 1980s, augmented during the 1990s in the United Kingdom by a cyclical decline in sea‐salt deposition. Our observational and experimental data demonstrate a clear, inverse and quantitatively important link between DOC and sulphate concentrations in soil solution. Statistical analysis of 11 AWMN lakes suggests that rising temperature, declining sulphur deposition and changing sea‐salt loading can account for the majority of the observed DOC trend. This combination of evidence points to the changing chemical composition of atmospheric deposition, particularly the substantial reduction in anthropogenic sulphur emissions during the last 20 years, as a key cause of rising DOC. The implications of rising DOC export for the carbon cycle will be very different if linked primarily to decreasing acid deposition, rather than to changes in climate, suggesting that these systems may be recovering rather than destabilising.     

Influence of hydrological pathways on dissolved organic carbon fluxes in tropical streams

Water flow pathways and water balance are fundamental components for understanding the dynamics of C in the soil/water interface of small basins. The objective of this study was to describe the seasonal variations and estimate the annual balance of dissolved organic carbon (DOC ) by comparing two tropical microbasins (preserved forest—PF and cacao plantation—CP ). Twenty‐one weekly collections were conducted from September to December 2012 and from April to June 2013. The calculation of the partial balance considered precipitation (P) as inflow and the stream as outflow. The samples were filtered and analyzed using a TOC analyzer. Overall, the DOC was higher CP compared with FP . The behavior of both venues showed that rainy season caused an increase in concentrations in the overland flow (OF ) and in the stream, and a decrease in the precipitation (P) and in the throughfall (T). In the CP , the outflow and the soil were chiefly responsible for the high DOC concentrations in the stream, when compared to the PF , which is the result of constant OM decomposition. Soil composition contributes to the control of DOC consumption in each type of soil. The balances were negative in both microbasins, although losses were higher in the AFS (agroforestry systems) when compared to the PF , especially during rainy seasons (?8.98 and ?3.05 kg ha^?1 year^?1, CP and FP , respectively). Thus, the high annual loss of DOC in the CP of the microbasins during the rainy season indicates changes in ecosystem metabolism due to the vegetation cover and to the interactions with the soil.     

Climate-induced changes in the dissolved organic carbon budgets of boreal lakes

During 20 years of climatic warming, drought and increased forest firesbetween 1970 and 1990, DOC concentrations declined by 15--25%in lakesof the Experimental Lakes Area, northwestern Ontario, allowing increasedpenetration of both UV and photosynthetically-active radiation (PAR), andcausing deeper euphotic zones and thermoclines. Decreased input to thelakes of DOC from terrestrial catchments and upstream lakes was theprimary reason for the decline, although in-lake removal also increasedslightly. Decreased streamflow caused by drought was more important thanforest fires in affecting DOC exports from catchments. Experimentalacidification of lakes caused even greater losses in DOC, by enhancing ratesof in-lake removal. DOC in Lake 302S, acidified to pH 4.5 during the1980s, declined to less than 10% of preacidificationvalues.     

The significance of storms for the concentration and export of dissolved organic carbon from two Precambrian Shield catchments

Dissolved organic carbon (DOC) concentrations and DOC export arestudied during storms to examine the relationship between DOCconcentration and stream discharge and to assess the importance of stormson DOC export. Storms were monitored in seven subcatchments within twosmall watersheds (Harp 4--21 and Harp 3A) on the Precambrian Shield inCentral Ontario, Canada. Stream DOC concentrations increase during stormsby as much as 100% and 410% in Harp3A and Harp 4--21 respectively. The seasonal regression between DOC andstream discharge is significant in subcatchments without wetlands(r² > 0.7) but is not significant in thetwo subcatchments with small wetland areas (r² <0.06). On average, regressions based on weekly data yield accurate estimatesof DOC export but the variation in regressions among individual storms andthe small number of high DOC samples result in uncertainties of more than30% in DOC export. The period-weighted calculation ofDOC export from weekly data underestimates export by 14%and 22% in Harp 3A and Harp 4--21 respectively. Stormswere responsible for 57% to 68% of theDOC export in the autumn and 29% to 40%of the DOC export in the spring. A single large storm accounted for31% of the autumn DOC export in Harp 3A. The importanceof individual storms for DOC export and the variation in the relationshipbetween DOC and stream discharge among storms make it difficult to predictthe effects of climate change on DOC export and DOC concentrations.     

土壤有机碳和氮分解对温度变化的响应趋势与研究方法

总结了土壤中碳和氮贮量与温度的关系、土壤碳和氮分解对温度时空差异和直接加热升温的响应,以及土壤碳和氮分解对低温冻结及冻融循环的响应趋势,讨论了其研究方法的误差和不确定性,并对今后的研究提出了一些建议．气候变暖在短期内将使土壤碳和氮分解加速并引起CO2释放量增加,而长期过程中却并不一定会引起土壤碳和氮分解加速．合理解释不同研究结果的差异,除了需要系统分析土壤碳和氮分解对温度变化响应的机制外,还需要充分认识土壤碳和氮分解对温度变化响应的长期过程和短期过程的差异,以及研究方法、植被、土壤和气候等因素的影响．     

Potential for detecting changes in soil organic carbon concentrations resulting from climate change

The interaction between soil organic carbon pools and climate change is an important determinant of future atmospheric CO₂ concentrations. Much effort has so far been allocated to manipulative process studies and predictive modelling exercises. Here, we examine the potential for directly detecting predicted changes through repeated soil sampling. Two contrasting benchmark plots were selected in the steppe at the Russian–Mongolian border, where soil organic carbon losses are predicted to be around 10% over the first 50 years of climate change. In both plots, 50 samples were taken to 20 and 30 cm depths. The estimated time intervals before re‐sampling by the same method that were likely to prove significant soil organic carbon losses (α=0.05; statistical power=0.90) were 43 and 26 years.     

Underestimated ecosystem carbon turnover time and sequestration under the steady state assumption: A perspective from long‐term data assimilation

It is critical to accurately estimate carbon (C) turnover time as it dominates the uncertainty in ecosystem C sinks and their response to future climate change. In the absence of direct observations of ecosystem C losses, C turnover times are commonly estimated under the steady state assumption (SSA), which has been applied across a large range of temporal and spatial scales including many at which the validity of the assumption is likely to be violated. However, the errors associated with improperly applying SSA to estimate C turnover time and its covariance with climate as well as ecosystem C sequestrations have yet to be fully quantified. Here, we developed a novel model‐data fusion framework and systematically analyzed the SSA‐induced biases using time‐series data collected from 10 permanent forest plots in the eastern China monsoon region. The results showed that (a) the SSA significantly underestimated mean turnover times (MTTs) by 29%, thereby leading to a 4.83‐fold underestimation of the net ecosystem productivity (NEP) in these forest ecosystems, a major C sink globally; (b) the SSA‐induced bias in MTT and NEP correlates negatively with forest age, which provides a significant caveat for applying the SSA to young‐aged ecosystems; and (c) the sensitivity of MTT to temperature and precipitation was 22% and 42% lower, respectively, under the SSA. Thus, under the expected climate change, spatiotemporal changes in MTT are likely to be underestimated, thereby resulting in large errors in the variability of predicted global NEP. With the development of observation technology and the accumulation of spatiotemporal data, we suggest estimating MTTs at the disequilibrium state via long‐term data assimilation, thereby effectively reducing the uncertainty in ecosystem C sequestration estimations and providing a better understanding of regional or global C cycle dynamics and C‐climate feedback.     

Terrestrial export of highly bioavailable carbon from small boreal catchments in spring floods

1. We assessed the terrestrial export of organic carbon, which effectively supported aquatic bacterial production (BP), from small boreal catchments during spring flood. We analysed stream runoff from nine small catchments with different proportions of peat mires and coniferous forests by monitoring the dissolved organic carbon (DOC) flux in combination with conducting bacterial bioassays.
2. Multiple linear regression analysis showed that BP during 7-day-dark bioassays (BP₇; μg C L⁻¹day⁻¹) was explained by both the quantity and quality (low-molecular weight fractions) of the DOC. BP₇ can be used as a measure of export of terrestrial organic carbon that is highly bioavailable.
3. Total export of DOC during spring flood from the different catchments ranged from 20 to 27 kg ha⁻¹ and was negatively correlated to forest cover (%). However, the export of BP₇ carbon was positively correlated to forest cover and varied from about 0.1 kg ha⁻¹ in mire-dominated streams to about 0.2 kg ha⁻¹ in forest-dominated streams.
4. The high bioavailability of forest carbon suggests that forests are the main contributors of BP-supporting carbon in boreal streams although mires have higher area-specific export of DOC.     

Controls of dissolved organic matter quality: evidence from a large‐scale boreal lake survey

Inland waters transport large amounts of dissolved organic matter (DOM) from terrestrial environments to the oceans, but DOM also reacts en route, with substantial water column losses by mineralization and sedimentation. For DOM transformations along the aquatic continuum, lakes play an important role as they retain waters in the landscape allowing for more time to alter DOM. We know DOM losses are significant at the global scale, yet little is known about how the reactivity of DOM varies across landscapes and climates. DOM reactivity is inherently linked to its chemical composition. We used fluorescence spectroscopy to explore DOM quality from 560 lakes distributed across Sweden and encompassed a wide climatic gradient typical of the boreal ecozone. Six fluorescence components were identified using parallel factor analysis (PARAFAC). The intensity and relative abundance of these components were analyzed in relation to lake chemistry, catchment, and climate characteristics. Land cover, particularly the percentage of water in the catchment, was a primary factor explaining variability in PARAFAC components. Likewise, lake water retention time influenced DOM quality. These results suggest that processes occurring in upstream water bodies, in addition to the lake itself, have a dominant influence on DOM quality. PARAFAC components with longer emission wavelengths, or red‐shifted components, were most reactive. In contrast, protein‐like components were most persistent within lakes. Generalized characteristics of PARAFAC components based on emission wavelength could ease future interpretation of fluorescence spectra. An important secondary influence on DOM quality was mean annual temperature, which ranged between ?6.2 and +7.5 °C. These results suggest that DOM reactivity depends more heavily on the duration of time taken to pass through the landscape, rather than temperature. Projected increases in runoff in the boreal region may force lake DOM toward a higher overall amount and proportion of humic‐like substances.     

Major limitations to achieving “4 per 1000” increases in soil organic carbon stock in temperate regions: Evidence from long‐term experiments at Rothamsted Research,United Kingdom

We evaluated the “4 per 1000” initiative for increasing soil organic carbon (SOC) by analysing rates of SOC increase in treatments in 16 long‐term experiments in southeast United Kingdom. The initiative sets a goal for SOC stock to increase by 4‰ per year in the 0–40 cm soil depth, continued over 20 years. Our experiments, on three soil types, provided 114 treatment comparisons over 7–157 years. Treatments included organic additions (incorporated by inversion ploughing), N fertilizers, introducing pasture leys into continuous arable systems, and converting arable land to woodland. In 65% of cases, SOC increases occurred at >7‰ per year in the 0–23 cm depth, approximately equivalent to 4‰ per year in the 0–40 cm depth. In the two longest running experiments (>150 years), annual farmyard manure (FYM) applications at 35 t fresh material per hectare (equivalent to approx. 3.2 t organic C/ha/year) gave SOC increases of 18‰ and 43‰ per year in the 23 cm depth during the first 20 years. Increases exceeding 7‰ per year continued for 40–60 years. In other experiments, with FYM applied at lower rates or not every year, there were increases of 3‰–8‰ per year over several decades. Other treatments gave increases between zero and 19‰ per year over various periods. We conclude that there are severe limitations to achieving the “4 per 1000” goal in practical agriculture over large areas. The reasons include (1) farmers not having the necessary resources (e.g. insufficient manure); (2) some, though not all, practices favouring SOC already widely adopted; (3) practices uneconomic for farmers—potentially overcome by changes in regulations or subsidies; (4) practices undesirable for global food security. We suggest it is more realistic to promote practices for increasing SOC based on improving soil quality and functioning as small increases can have disproportionately large beneficial impacts, though not necessarily translating into increased crop yield.     

Long‐term carbon storage through retention of dissolved aromatic acids by reactive particles in soil

Soils retain large quantities of carbon, thereby slowing its return to the atmosphere. The mechanisms governing organic carbon sequestration in soil remain poorly understood, yet are integral to understanding soil‐climate feedbacks. We evaluated the biochemistry of dissolved and solid organic carbon in potential source and sink horizons across a chronosequence of volcanic soils in Hawai'i. The soils are derived from similar basaltic parent material on gently sloping volcanic shield surfaces, support the same vegetation assemblage, and yet exhibit strong shifts in soil mineralogy and soil carbon content as a function of volcanic substrate age. Solid‐state¹³carbon nuclear magnetic resonance spectra indicate that the most persistent mineral‐bound carbon is comprised of partially oxidized aromatic compounds with strong chemical resemblance to dissolved organic matter derived from plant litter. A molecular mixing model indicates that protein, lipid, carbohydrate, and char content decreased whereas oxidized lignin and carboxyl/carbonyl content increased with increasing short‐range order mineral content. When solutions rich in dissolved organic matter were passed through Bw‐horizon mineral cores, aromatic compounds were preferentially sorbed with the greatest retention occurring in horizons containing the greatest amount of short‐range ordered minerals. These minerals are reactive metastable nanocrystals that are most common in volcanic soils, but exist in smaller amounts in nearly all major soil classes. Our results indicate that long‐term carbon storage in short‐range ordered minerals occurs via chemical retention with dissolved aromatic acids derived from plant litter and carried along preferential flow‐paths to deeper B horizons.     

Soil carbon sequestration due to post‐Soviet cropland abandonment: estimates from a large‐scale soil organic carbon field inventory

The break‐up of the Soviet Union in 1991 triggered cropland abandonment on a continental scale, which in turn led to carbon accumulation on abandoned land across Eurasia. Previous studies have estimated carbon accumulation rates across Russia based on large‐scale modelling. Studies that assess carbon sequestration on abandoned land based on robust field sampling are rare. We investigated soil organic carbon (SOC) stocks using a randomized sampling design along a climatic gradient from forest steppe to Sub‐Taiga in Western Siberia (Tyumen Province). In total, SOC contents were sampled on 470 plots across different soil and land‐use types. The effect of land use on changes in SOC stock was evaluated, and carbon sequestration rates were calculated for different age stages of abandoned cropland. While land‐use type had an effect on carbon accumulation in the topsoil (0–5 cm), no independent land‐use effects were found for deeper SOC stocks. Topsoil carbon stocks of grasslands and forests were significantly higher than those of soils managed for crops and under abandoned cropland. SOC increased significantly with time since abandonment. The average carbon sequestration rate for soils of abandoned cropland was 0.66 Mg C ha^?1 yr^?1 (1–20 years old, 0–5 cm soil depth), which is at the lower end of published estimates for Russia and Siberia. There was a tendency towards SOC saturation on abandoned land as sequestration rates were much higher for recently abandoned (1–10 years old, 1.04 Mg C ha^?1 yr^?1) compared to earlier abandoned crop fields (11–20 years old, 0.26 Mg C ha^?1 yr^?1). Our study confirms the global significance of abandoned cropland in Russia for carbon sequestration. Our findings also suggest that robust regional surveys based on a large number of samples advance model‐based continent‐wide SOC prediction.     

Enhanced decomposition of stable soil organic carbon and microbial catabolic potentials by long‐term field warming

Quantifying soil organic carbon (SOC) decomposition under warming is critical to predict carbon–climate feedbacks. According to the substrate regulating principle, SOC decomposition would decrease as labile SOC declines under field warming, but observations of SOC decomposition under warming do not always support this prediction. This discrepancy could result from varying changes in SOC components and soil microbial communities under warming. This study aimed to determine the decomposition of SOC components with different turnover times after subjected to long‐term field warming and/or root exclusion to limit C input, and to test whether SOC decomposition is driven by substrate lability under warming. Taking advantage of a 12‐year field warming experiment in a prairie, we assessed the decomposition of SOC components by incubating soils from control and warmed plots, with and without root exclusion for 3 years. We assayed SOC decomposition from these incubations by combining inverse modeling and microbial functional genes during decomposition with a metagenomic technique (GeoChip). The decomposition of SOC components with turnover times of years and decades, which contributed to 95% of total cumulative CO₂ respiration, was greater in soils from warmed plots. But the decomposition of labile SOC was similar in warmed plots compared to the control. The diversity of C‐degradation microbial genes generally declined with time during the incubation in all treatments, suggesting shifts of microbial functional groups as substrate composition was changing. Compared to the control, soils from warmed plots showed significant increase in the signal intensities of microbial genes involved in degrading complex organic compounds, implying enhanced potential abilities of microbial catabolism. These are likely responsible for accelerated decomposition of SOC components with slow turnover rates. Overall, the shifted microbial community induced by long‐term warming accelerates the decomposition of SOC components with slow turnover rates and thus amplify the positive feedback to climate change.     

Response of soil carbon dioxide fluxes,soil organic carbon and microbial biomass carbon to biochar amendment: a meta‐analysis

Biochar as a carbon‐rich coproduct of pyrolyzing biomass, its amendment has been advocated as a potential strategy to soil carbon (C) sequestration. Updated data derived from 50 papers with 395 paired observations were reviewed using meta‐analysis procedures to examine responses of soil carbon dioxide (CO₂) fluxes, soil organic C (SOC), and soil microbial biomass C (MBC) contents to biochar amendment. When averaged across all studies, biochar amendment had no significant effect on soil CO₂ fluxes, but it significantly enhanced SOC content by 40% and MBC content by 18%. A positive response of soil CO₂ fluxes to biochar amendment was found in rice paddies, laboratory incubation studies, soils without vegetation, and unfertilized soils. Biochar amendment significantly increased soil MBC content in field studies, N‐fertilized soils, and soils with vegetation. Enhancement of SOC content following biochar amendment was the greatest in rice paddies among different land‐use types. Responses of soil CO₂ fluxes and MBC to biochar amendment varied with soil texture and pH. The use of biochar in combination with synthetic N fertilizer and waste compost fertilizer led to the greatest increases in soil CO₂ fluxes and MBC content, respectively. Both soil CO₂ fluxes and MBC responses to biochar amendment decreased with biochar application rate, pyrolysis temperature, or C/N ratio of biochar, while each increased SOC content enhancement. Among different biochar feedstock sources, positive responses of soil CO₂ fluxes and MBC were the highest for manure and crop residue feedstock sources, respectively. Soil CO₂ flux responses to biochar amendment decreased with pH of biochar, while biochars with pH of 8.1–9.0 had the greatest enhancement of SOC and MBC contents. Therefore, soil properties, land‐use type, agricultural practice, and biochar characteristics should be taken into account to assess the practical potential of biochar for mitigating climate change.     

Predicting long‐term carbon mineralization and trace gas production from thawing permafrost of Northeast Siberia

The currently observed Arctic warming will increase permafrost degradation followed by mineralization of formerly frozen organic matter to carbon dioxide (CO₂) and methane (CH₄). Despite increasing awareness of permafrost carbon vulnerability, the potential long‐term formation of trace gases from thawing permafrost remains unclear. The objective of the current study is to quantify the potential long‐term release of trace gases from permafrost organic matter. Therefore, Holocene and Pleistocene permafrost deposits were sampled in the Lena River Delta, Northeast Siberia. The sampled permafrost contained between 0.6% and 12.4% organic carbon. CO₂ and CH₄ production was measured for 1200 days in aerobic and anaerobic incubations at 4 °C. The derived fluxes were used to estimate parameters of a two pool carbon degradation model. Total CO₂ production was similar in Holocene permafrost (1.3 ± 0.8 mg CO₂‐C gdw^?1 aerobically, 0.25 ± 0.13 mg CO₂‐C gdw^?1 anaerobically) as in 34 000–42 000‐year‐old Pleistocene permafrost (1.6 ± 1.2 mg CO₂‐C gdw^?1 aerobically, 0.26 ± 0.10 mg CO₂‐C gdw^?1 anaerobically). The main predictor for carbon mineralization was the content of organic matter. Anaerobic conditions strongly reduced carbon mineralization since only 25% of aerobically mineralized carbon was released as CO₂ and CH₄ in the absence of oxygen. CH₄ production was low or absent in most of the Pleistocene permafrost and always started after a significant delay. After 1200 days on average 3.1% of initial carbon was mineralized to CO₂ under aerobic conditions while without oxygen 0.55% were released as CO₂ and 0.28% as CH₄. The calibrated carbon degradation model predicted cumulative CO₂ production over a period of 100 years accounting for 15.1% (aerobic) and 1.8% (anaerobic) of initial organic carbon, which is significantly less than recent estimates. The multiyear time series from the incubation experiments helps to more reliably constrain projections of future trace gas fluxes from thawing permafrost landscapes.     

气候变化对陆地生态系统土壤有机碳储量变化的影响

通过研究气候变化对土壤有机碳储藏的影响,对预测未来气候变化下土壤有机碳动态变化与深入理解陆地生态系统变化和气候变化之间的相互作用有着极其重要的意义。本文归纳了土壤类型法、模型模拟法等途径对土壤有机碳储量估算的结果并分析它们各自的不确定性,综述了气候变化对土壤碳贮藏影响机理的研究与相应过程模拟的模型研究进展,并综合分析了当前研究中还存在的问题与不足。     

Almost 50 years of monitoring shows that climate,not forestry,controls long‐term organic carbon fluxes in a large boreal watershed

Here, we use a unique long‐term data set on total organic carbon (TOC) fluxes, its climatic drivers and effects of land management from a large boreal watershed in northern Finland. TOC and runoff have been monitored at several sites in the Simojoki watershed (3160 km²) since the early 1960s. Annual TOC fluxes have increased significantly together with increased inter‐annual variability. Acid deposition in the area has been low and has not significantly influenced losses of TOC. Forest management, including ditching and clear felling, had a minor influence on TOC fluxes – seasonal and long‐term patterns in TOC were controlled primarily by changes in soil frost, seasonal precipitation, drought, and runoff. Deeper soil frost led to lower spring TOC concentrations in the river. Summer TOC concentrations were positively correlated with precipitation and soil moisture not temperature. There is some indication that drought conditions led to elevated TOC concentrations and fluxes in subsequent years (1998–2000). A sensitivity analysis of the INCA‐C model results showed the importance of landscape position, land‐use type, and soil temperature as controls of modeled TOC concentrations. Model predictions were not sensitive to forest management. Our results are contradictory to some earlier plot‐scale and small catchment studies that have shown more profound forest management impacts on TOC fluxes. This shows the importance of scale when assessing the mechanisms controlling TOC fluxes and concentrations. The results highlight the value of long‐term multiple data sets to better understand ecosystem response to land management, climate change and extremes in northern ecosystems.     

Greenhouse gas mitigation potential in crop production with biochar soil amendment—a carbon footprint assessment for cross‐site field experiments from China

Biochar soil amendment (BSA) had been advocated as a promising approach to mitigate greenhouse gas (GHG) emissions in agriculture. However, the net GHG mitigation potential of BSA remained unquantified with regard to the manufacturing process and field application. Carbon footprint (CF) was employed to assess the mitigating potential of BSA by estimating all the direct and indirect GHG emissions in the full life cycles of crop production including production and field application of biochar. Data were obtained from 7 sites (4 sites for paddy rice production and 3 sites for maize production) under a single BSA at 20 t/ha^?1 across mainland China. Considering soil organic carbon (SOC) sequestration and GHG emission reduction from syngas recycling, BSA reduced the CFs by 20.37–41.29 t carbon dioxide equivalent ha^?1 (CO₂‐eq ha^?1) and 28.58–39.49 t CO₂‐eq ha^?1 for paddy rice and maize production, respectively, compared to no biochar application. Without considering SOC sequestration and syngas recycling, the net CF change by BSA was in a range of ?25.06 to 9.82 t CO₂‐eq ha^?1 and ?20.07 to 5.95 t CO₂‐eq ha^?1 for paddy rice and maize production, respectively, over no biochar application. As the largest contributors among the others, syngas recycling in the process of biochar manufacture contributed by 47% to total CF reductions under BSA for rice cultivation while SOC sequestration contributed by 57% for maize cultivation. There was a large variability of the CF reductions across the studied sites whether in paddy rice or maize production, due likely to the difference in GHG emission reductions and SOC increments under BSA across the sites. This study emphasized that SOC sequestration should be taken into account the CF calculation of BSA. Improved biochar manufacturing technique could achieve a remarkable carbon sink by recycling the biogas for traditional fossil‐fuel replacement.     

Short‐term carbon cycling responses of a mature eucalypt woodland to gradual stepwise enrichment of atmospheric CO2 concentration

Projections of future climate are highly sensitive to uncertainties regarding carbon (C) uptake and storage by terrestrial ecosystems. The Eucalyptus Free‐Air CO₂ Enrichment (EucFACE) experiment was established to study the effects of elevated atmospheric CO₂ concentrations (eCO₂) on a native mature eucalypt woodland with low fertility soils in southeast Australia. In contrast to other FACE experiments, the concentration of CO₂ at EucFACE was increased gradually in steps above ambient (+0, 30, 60, 90, 120, and 150 ppm CO₂ above ambient of ~400 ppm), with each step lasting approximately 5 weeks. This provided a unique opportunity to study the short‐term (weeks to months) response of C cycle flux components to eCO₂ across a range of CO₂ concentrations in an intact ecosystem. Soil CO₂ efflux (i.e., soil respiration or R_soil) increased in response to initial enrichment (e.g., +30 and +60 ppm CO₂) but did not continue to increase as the CO₂ enrichment was stepped up to higher concentrations. Light‐saturated photosynthesis of canopy leaves (A_sat) also showed similar stimulation by elevated CO₂ at +60 ppm as at +150 ppm CO₂. The lack of significant effects of eCO₂ on soil moisture, microbial biomass, or activity suggests that the increase in R_soil likely reflected increased root and rhizosphere respiration rather than increased microbial decomposition of soil organic matter. This rapid increase in R_soil suggests that under eCO_2, additional photosynthate was produced, transported belowground, and respired. The consequences of this increased belowground activity and whether it is sustained through time in mature ecosystems under eCO₂ are a priority for future research.