The organic carbon dynamics of a moorland catchment in N. W. England

The carbon cycle was quantified in the catchment of Doe House Gill, which drains high-relief moorland, with thin organic-rich soils (leptosols and podzols) 10–25 cm deep, in northern England. The soil C pool of 8,300 g m^-2 is due mainly to humic acid and older humin. If steady state is assumed, and a single soil C pool, the average ¹⁴C content of the whole soil (93% modern) yields a mean carbon residence time of 800 years, although this varied from 300 to 1,600 years in the four samples studied. Stream water fluxes of dissolved and particulate organic carbon (DOC, POC) were 2.5 and 0.4 g m⁻² a⁻¹ respectively in 2002–2003, lower than values for some other upland streams in the UK. The C pool, flux, and isotope data were used, with the assumption of steady state, to calibrate DyDOC, a model that simulates the soil carbon cycle, including the generation and transport of DOC. According to DyDOC, the litter pool (ca. 100 gC m⁻²) turns over quickly, and most (>90%) of the litter carbon is rapidly mineralised. The soil is calculated to gain only 16 gC m⁻² a⁻¹, and to lose the same amount, about 80% as CO₂ and 20% as DOC. From the DO¹⁴C content of 107.5% modern (due to “bomb carbon”) the model could be calibrated by assuming all DOC to come directly from litter, but DOC is more likely a mixture, derived from more than one soil C pool. The seasonal variability exhibited by stream water DOC concentration (maximum in September, minimum in January) is attributed mainly to variations in rainfall and evapotranspiration, rather than in the metabolic production rate of “potential DOC”. The model predicts that, for a Q ₁₀ of 2, the total soil organic C pool would decrease by about 5% if subjected to warming over 200 years. DyDOC predicts higher DOC fluxes in response to increased litter inputs or warming, and can simulate changes in DOC flux due to variations in sorption to soil solids, that might occur due to acidification and its reversal.     

Modelling the production and transport of dissolved organic carbon in forest soils

DyDOC describes soil carbon dynamics, with a focus on dissolved organic carbon (DOC). The model treats the soil as a three-horizon profile, and simulates metabolic carbon transformations, sorption reactions and water transport. Humic substances are partitioned into three fractions, one of which is immobile, while the other two (hydrophilic and hydrophobic) can pass into solution as DOC. DyDOC requires site-specific soil characteristics, and is driven by inputs of litter and water, and air and soil temperatures. The model operates on hourly and daily time steps, and can simulate carbon cycling over both long (hundreds-to-thousands of years) and short (daily) time scales. An important feature of DyDOC is the tracking of ¹⁴C, from its entry in litter to its loss as DO¹⁴C in drainage water, enabling information about C dynamics to be obtained from both long-term radioactive decay, and the characteristic ¹⁴C pulse caused by thermonuclear weapon testing during the 1960s ("bomb carbon"). Parameterisation is performed by assuming a current steady state. Values of a range of variables, including C pools, annual DOC fluxes, and ¹⁴C signals, are combined into objective functions for least-squares minimisation. DyDOC has been applied successfully to spruce forest sites at Birkenes (Norway) and Waldstein (Germany), and most of the parameters have similar values at the two sites. The results indicate that the supply of DOC from the surface soil horizon to percolating water depends upon the continual metabolic production of easily leached humic material. In contrast, concentrations and fluxes of DOC in the deeper soil horizons are controlled by sorption processes, involving comparatively large pools of leachable organic matter. Times to reach steady state are calculated to be several hundred years in the organic layer, and hundreds-to-thousands of years in the deeper mineral layers. It is estimated that DOC supplies 89% of the mineral soil carbon at Birkenes, and 73% at Waldstein. The model, parameterised with "steady state" data, simulates short-term variations in DOC concentrations and fluxes, and in DO¹⁴C, which are in approximate agreement with observations.     

An improved analysis of forest carbon dynamics using data assimilation

There are two broad approaches to quantifying landscape C dynamics – by measuring changes in C stocks over time, or by measuring fluxes of C directly. However, these data may be patchy, and have gaps or biases. An alternative approach to generating C budgets has been to use process‐based models, constructed to simulate the key processes involved in C exchange. However, the process of model building is arguably subjective, and parameters may be poorly defined. This paper demonstrates why data assimilation (DA) techniques – which combine stock and flux observations with a dynamic model – improve estimates of, and provide insights into, ecosystem carbon (C) exchanges. We use an ensemble Kalman filter (EnKF) to link a series of measurements with a simple box model of C transformations. Measurements were collected at a young ponderosa pine stand in central Oregon over a 3‐year period, and include eddy flux and soil CO₂ efflux data, litterfall collections, stem surveys, root and soil cores, and leaf area index data. The simple C model is a mass balance model with nine unknown parameters, tracking changes in C storage among five pools; foliar, wood and fine root pools in vegetation, and also fresh litter and soil organic matter (SOM) plus coarse woody debris pools. We nested the EnKF within an optimization routine to generate estimates from the data of the unknown parameters and the five initial conditions for the pools. The efficacy of the DA process can be judged by comparing the probability distributions of estimates produced with the EnKF analysis vs. those produced with reduced data or model alone. Using the model alone, estimated net ecosystem exchange of C (NEE)=?251±197 g C m^?2 over the 3 years, compared with an estimate of ?419±29 g C m^?2 when all observations were assimilated into the model. The uncertainty on daily measurements of NEE via eddy fluxes was estimated at 0.5 g C m^?2 day^?1, but the uncertainty on assimilated estimates averaged 0.47 g C m^?2 day^?1, and only exceeded 0.5 g C m^?2 day^?1 on days where neither eddy flux nor soil efflux data were available. In generating C budgets, the assimilation process reduced the uncertainties associated with using data or model alone and the forecasts of NEE were statistically unbiased estimates. The results of the analysis emphasize the importance of time series as constraints. Occasional, rare measurements of stocks have limited use in constraining the estimates of other components of the C cycle. Long time series are particularly crucial for improving the analysis of pools with long time constants, such as SOM, woody biomass, and woody debris. Long‐running forest stem surveys, and tree ring data, offer a rich resource that could be assimilated to provide an important constraint on C cycling of slow pools. For extending estimates of NEE across regions, DA can play a further important role, by assimilating remote‐sensing data into the analysis of C cycles. We show, via sensitivity analysis, how assimilating an estimate of photosynthesis – which might be provided indirectly by remotely sensed data – improves the analysis of NEE.     

Soil carbon cycling in a temperate forest: radiocarbon-based estimates of residence times, sequestration rates and partitioning of fluxes

Temperate forests of North America are thought to besignificant sinks of atmospheric CO₂. Wedeveloped a below-ground carbon (C) budget forwell-drained soils in Harvard Forest Massachusetts, anecosystem that is storing C. Measurements of carbonand radiocarbon (¹⁴C) inventory were used todetermine the turnover time and maximum rate ofCO₂ production from heterotrophic respiration ofthree fractions of soil organic matter (SOM):recognizable litter fragments (L), humified lowdensity material (H), and high density ormineral-associated organic matter (M). Turnover timesin all fractions increased with soil depth and were2–5 years for recognizable leaf litter, 5–10 years forroot litter, 40–100+ years for low density humifiedmaterial and >100 years for carbon associated withminerals. These turnover times represent the timecarbon resides in the plant + soil system, and mayunderestimate actual decomposition rates if carbonresides for several years in living root, plant orwoody material.Soil respiration was partitioned into two componentsusing ¹⁴C: recent photosynthate which ismetabolized by roots and microorganisms within a yearof initial fixation (Recent-C), and C that is respiredduring microbial decomposition of SOM that resides inthe soil for several years or longer (Reservoir-C).For the whole soil, we calculate that decomposition ofReservoir-C contributes approximately 41% of thetotal annual soil respiration. Of this 41%,recognizable leaf or root detritus accounts for 80%of the flux, and 20% is from the more humifiedfractions that dominate the soil carbon stocks.Measurements of CO₂ and ¹⁴CO₂ in thesoil atmosphere and in total soil respiration werecombined with surface CO₂ fluxes and a soil gasdiffusion model to determine the flux and isotopicsignature of C produced as a function of soil depth. 63% of soil respiration takes place in the top 15 cmof the soil (O + A + Ap horizons). The average residencetime of Reservoir-C in the plant + soil system is8±1 years and the average age of carbon in totalsoil respiration (Recent-C + Reservoir-C) is 4±1years.The O and A horizons have accumulated 4.4 kgC m^–2above the plow layer since abandonment by settlers inthe late-1800's. C pools contributing the most to soilrespiration have short enough turnover times that theyare likely in steady state. However, most C is storedas humified organic matter within both the O and Ahorizons and has turnover times from 40 to 100+ yearsrespectively. These reservoirs continue to accumulatecarbon at a combined rate of 10–30 gC m^{minus 2}yr^–1. This rate of accumulation is only 5–15% of the total ecosystem C sink measured in this stand using eddy covariance methods.     

Nitrogen addition alters mineralization dynamics of 13C‐depleted leaf and twig litter and reduces leaching of older DOC from mineral soil

Recent reviews indicate that N deposition increases soil organic matter (SOM) storage in forests but the undelying processes are poorly understood. Our aim was to quantify the impacts of increased N inputs on soil C fluxes such as C mineralization and leaching of dissolved organic carbon (DOC) from different litter materials and native SOM. We added 5.5 g N m^?2 yr^?1 as NH₄NO₃ over 1 year to two beech forest stands on calcareous soils in the Swiss Jura. We replaced the native litter layer with ¹³C‐depleted twigs and leaves (δ¹³C: ?38.4 and ?40.8‰) in late fall and measured N effects on litter‐ and SOM‐derived C fluxes. Nitrogen addition did not significantly affect annual C losses through mineralization, but altered the temporal dynamics in litter mineralization: increased N inputs stimulated initial mineralization during winter (leaves: +25%; twigs: +22%), but suppressed rates in the subsequent summer. The switch from a positive to a negative response occurred earlier and more strongly for leaves than for twigs (?21% vs. 0%). Nitrogen addition did not influence microbial respiration from the nonlabeled calcareous mineral soil below the litter which contrasts with recent meta‐analysis primarily based on acidic soils. Leaching of DOC from the litter layer was not affected by NH₄NO₃ additions, but DOC fluxes from the mineral soils at 5 and 10 cm depth were significantly reduced by 17%. The ¹³C tracking indicated that litter‐derived C contributed less than 15% of the DOC flux from the mineral soil, with N additions not affecting this fraction. Hence, the suppressed DOC fluxes from the mineral soil at higher N inputs can be attributed to reduced mobilization of nonlitter derived ‘older’ DOC. We relate this decline to an altered solute chemistry by NH₄NO₃ additions, an increased ionic strength and acidification resulting from nitrification, rather than to a change in microbial decomposition.     

Partitioning sources of soil-respired CO2 and their seasonal variation using a unique radiocarbon tracer

Soil respiration is derived from heterotrophic (decomposition of soil organic matter) and autotrophic (root/rhizosphere respiration) sources, but there is considerable uncertainty about what factors control variations in their relative contributions in space and time. We took advantage of a unique whole‐ecosystem radiocarbon label in a temperate forest to partition soil respiration into three sources: (1) recently photosynthesized carbon (C), which dominates root and rhizosphere respiration; (2) leaf litter decomposition and (3) decomposition of root litter and soil organic matter >1–2 years old. Heterotrophic sources and specifically leaf litter decomposition were large contributors to total soil respiration during the growing season. Relative contributions from leaf litter decomposition ranged from a low of ～1±3% of total soil respiration (6± 3 mg C m^?2 h^?1) when leaf litter was extremely dry, to a high of 42±16% (96± 38 mg C m^?2 h^?1). Total soil respiration fluxes varied with the strength of the leaf litter decomposition source, indicating that moisture‐dependent changes in litter decomposition drive variability in total soil respiration fluxes. In the surface mineral soil layer, decomposition of C fixed in the original labeling event (3–5 years earlier) dominated the isotopic signature of heterotrophic respiration. Root/rhizosphere respiration accounted for 16±10% to 64±22% of total soil respiration, with highest relative contributions coinciding with low overall soil respiration fluxes. In contrast to leaf litter decomposition, root respiration fluxes did not exhibit marked temporal variation ranging from 34±14 to 40±16 mg C m^?2 h^?1 at different times in the growing season with a single exception (88±35 mg C m^?2 h^?1). Radiocarbon signatures of root respired CO₂ changed markedly between early and late spring (March vs. May), suggesting a switch from stored nonstructural carbohydrate sources to more recent photosynthetic products.     

Soil carbon and belowground carbon balance of a short‐rotation coppice: assessments from three different approaches

Uncertainty in soil carbon (C) fluxes across different land‐use transitions is an issue that needs to be addressed for the further deployment of perennial bioenergy crops. A large‐scale short‐rotation coppice (SRC) site with poplar (Populus) and willow (Salix) was established to examine the land‐use transitions of arable and pasture to bioenergy. Soil C pools, output fluxes of soil CO₂, CH₄, dissolved organic carbon (DOC) and volatile organic compounds, as well as input fluxes from litter fall and from roots, were measured over a 4‐year period, along with environmental parameters. Three approaches were used to estimate changes in the soil C. The largest C pool in the soil was the soil organic carbon (SOC) pool and increased after four years of SRC from 10.9 to 13.9 kg C m^?2. The belowground woody biomass (coarse roots) represented the second largest C pool, followed by the fine roots (Fr). The annual leaf fall represented the largest C input to the soil, followed by weeds and Fr. After the first harvest, we observed a very large C input into the soil from high Fr mortality. The weed inputs decreased as trees grew older and bigger. Soil respiration averaged 568.9 g C m^?2 yr^?1. Leaching of DOC increased over the three years from 7.9 to 14.5 g C m^?2. The pool‐based approach indicated an increase of 3360 g C m^?2 in the SOC pool over the 4‐year period, which was high when compared with the ?27 g C m^?2 estimated by the flux‐based approach and the ?956 g C m^?2 of the combined eddy‐covariance + biometric approach. High uncertainties were associated to the pool‐based approach. Our results suggest using the C flux approach for the assessment of the short‐/medium‐term SOC balance at our site, while SOC pool changes can only be used for long‐term C balance assessments.     

The European carbon balance. Part 2: croplands

We estimated the long‐term carbon balance [net biome production (NBP)] of European (EU‐25) croplands and its component fluxes, over the last two decades. Net primary production (NPP) estimates, from different data sources ranged between 490 and 846 gC m^?2 yr^?1, and mostly reflect uncertainties in allocation, and in cropland area when using yield statistics. Inventories of soil C change over arable lands may be the most reliable source of information on NBP, but inventories lack full and harmonized coverage of EU‐25. From a compilation of inventories we infer a mean loss of soil C amounting to 17 g m^?2 yr^?1. In addition, three process‐based models, driven by historical climate and evolving agricultural technology, estimate a small sink of 15 g C m^?2 yr^?1 or a small source of 7.6 g C m^?2 yr^?1. Neither the soil C inventory data, nor the process model results support the previous European‐scale NBP estimate by Janssens and colleagues of a large soil C loss of 90 ± 50 gC m^?2 yr^?1. Discrepancy between measured and modeled NBP is caused by erosion which is not inventoried, and the burning of harvest residues which is not modeled. When correcting the inventory NBP for the erosion flux, and the modeled NBP for agricultural fire losses, the discrepancy is reduced, and cropland NBP ranges between ?8.3 ± 13 and ?13 ± 33 g C m^?2 yr^?1 from the mean of the models and inventories, respectively. The mean nitrous oxide (N₂O) flux estimates ranges between 32 and 37 g C Eq m^?2 yr^?1, which nearly doubles the CO₂ losses. European croplands act as small CH₄ sink of 3.3 g C Eq m^?2 yr^?1. Considering ecosystem CO₂, N₂O and CH₄ fluxes provides for the net greenhouse gas balance a net source of 42–47 g C Eq m^?2 yr^?1. Intensifying agriculture in Eastern Europe to the same level Western Europe amounts is expected to result in a near doubling of the N₂O emissions in Eastern Europe. N₂O emissions will then become the main source of concern for the impact of European agriculture on climate.     

百年尺度地球系统模式模拟的陆地生态系统碳通量对CO2浓度升高和气候变化的响应

利用了加拿大地球系统模式CanE SM2(Canadian Earth System Model of the CCCma)的结果,针对百年尺度大气CO_2浓度升高和气候变化如何影响陆地生态系统碳通量这一问题,分析了1850—1989年间陆地生态系统碳通量趋势对二者响应,以及与关键气候系统变量的关系。结果表明,140年间,当仅仅考虑CO_2浓度升高影响时,陆地生态系统净初级生产力(NPP)增加了117.1 gC m~(-2)a~(-1),土壤呼吸(Rh)增加了98.4 gC m~(-2)a~(-1),净生态系统生产力(NEP)平均增加了18.7 gC m~(-2)a~(-1)。相同情景下,全球陆地生态系统的NPP呈显著增加的线性趋势(约为0.30 PgC/a~2),Rh同样呈显著增加线性趋势(约为0.25 PgC/a~2)。仅仅考虑气候变化单独影响时,NPP平均减少了19.3 gC/m~2,土壤呼吸减少了8.5 gC/m~2,NEP减少了10.8 gC/m~2。在此情景下,整个陆地生态系统的NPP线性变化趋势约为-0.07 PgC/a~2(P0.05),Rh线性变化趋势约为-0.04 PgC/a~2(P0.05)。综合二者的影响,前者是决定陆地生态系统碳通量变化幅度和空间分布的最重要影响因子,其影响明显大于气候变化。值得注意的是,CanE SM2并没有考虑氮素的限制作用,所以CO_2浓度升高对植被的助长作用可能被高估。此外,气候变化的贡献也不容忽视,特别是在亚马逊流域,由于当温度升高、降水和土壤湿度减少,NPP和Rh均呈显著减少趋势。     

Crop residue-derived dissolved organic matter accelerates the decomposition of native soil organic carbon in a temperate agricultural ecosystem

Crop residue-derived dissolved organic matter (DOM) plays an important role in soil carbon (C) cycling. To investigate the effects of maize residue-derived DOM and urea additions on the native soil organic carbon (SOC) decomposition and soil net C balance a pot experiment was carried out during the winter wheat growing season in the North China Plain (NCP). The results showed that adding maize residue-derived DOM alone (RDOM) or together with urea (RDOM?+?N) accelerated the decomposition of native SOC and resulted in a net SOC loss. The net loss of SOC was 3.90?±?0.61 and 3.53?±?0.48?g?C?m^?2 in RDOM and RDOM?+?N treatments, respectively. The stimulatory effect of per unit DOM-C addition on the native SOC decomposition was 0.25?±?0.05 and 0.45?±?0.07 for the RDOM and RDOM?+?N treatments, respectively. Increases in the microbial biomass and the activity of β-glucosidase, invertase and cellobiohydrolase as well as soil mineral N content were responsible for a more intense priming effect in DOM-amended soils. The positive relationship between primed soil C and soil available N (R?=?0.76, P?<?0.05) suggested that the stimulation of decomposition of native SOC by DOM addition would be enhanced by nitrogen fertilizer application.     

Decadal cycling within long-lived carbon pools revealed by dual isotopic analysis of mineral-associated soil organic matter

Long-lived soil organic matter (SOM) pools are critical for the global carbon (C) cycle, but challenges in isolating such pools have inhibited understanding of their dynamics. We physically isolated particulate (>53 μm), silt-, and clay-sized organic matter from soils collected over two decades from a perennial C₃ grassland established on long-term agricultural soil with a predominantly C₄ isotopic signature. Silt- and clay-sized fractions were then subjected to a sequential chemical fractionation (acid hydrolysis followed by peroxide oxidation) to isolate long-lived C pools. We quantified ¹⁴C and the natural ¹³C isotopic label in the resulting fractions to identify and evaluate pools responsible for long-lived SOM. After removal of particulate organic matter (~14% of bulk soil C) sequential chemical treatment removed 80% of mineral-associated C. In all mineral-associated fractions, at least 55% of C₄-derived C was retained 32 years after the switch to C₃ inputs. However, C₃–C increased substantially beginning ~25 years after the switch. Radiocarbon-based turnover times ranged from roughly 1200–3000 years for chemically resistant mineral-associated pools, although some pools turned over faster under C₃ grassland than in a reference agricultural field, indicating that new material had entered some pools as early as 14 years after the vegetation switch. These findings provide further evidence that SOM chemistry does not always reflect SOM longevity and resistance to microbial decomposition. Even measureable SOM fractions that have extremely long mean turnover times (>1500 years) can have a substantial component that is dynamic over much shorter timescales.     

Net ecosystem carbon exchange in two experimental grassland ecosystems

Increases in net primary production (NPP) may not necessarily result in increased C sequestration since an increase in uptake can be negated by concurrent increases in ecosystem C losses via respiratory processes. Continuous measurements of net ecosystem C exchange between the atmosphere and two experimental cheatgrass (Bromus tectorum L.) ecosystems in large dynamic flux chambers (EcoCELLs) showed net ecosystem C losses to the atmosphere in excess of 300 g C m^?2 over two growing cycles. Even a doubling of net ecosystem production (NEP) after N fertilization in the second growing season did not compensate for soil C losses incurred during the fallow period. Fertilization not only increased C uptake in biomass but also enhanced C losses through soil respiration from 287 to 469 g C m^?2, mainly through an increase in rhizosphere respiration. Fertilization decreased dissolved inorganic C losses through leaching of from 45 to 10 g C m^?2. Unfertilized cheatgrass added 215 g C m^?2 as root‐derived organic matter but the contribution of these inputs to long‐term C sequestration was limited as these deposits rapidly decomposed. Fertilization increased NEP but did not increase belowground C inputs most likely due to a concurrent increase in the production and decomposition of rhizodeposits. Decomposition of soil organic matter (SOM) was reduced by fertilizer additions. The results from our study show that, although annual grassland ecosystems can add considerable amounts of C to soils during the growing season, it is unlikely that they sequester large amounts of C because of high respiratory losses during dormancy periods. Although fertilization could increase NEP, fertilization might reduce soil C inputs as heterotrophic organisms favor root‐derived organic matter over native SOM.     

Connecting carbon and nitrogen storage in rural wetland soil to groundwater abstraction for urban water supply

We investigated whether groundwater abstraction for urban water supply diminishes the storage of carbon (C), nitrogen (N), and organic matter in the soil of rural wetlands. Wetland soil organic matter (SOM) benefits air and water quality by sequestering large masses of C and N. Yet, the accumulation of wetland SOM depends on soil inundation, so we hypothesized that groundwater abstraction would diminish stocks of SOM, C, and N in wetland soils. Predictions of this hypothesis were tested in two types of subtropical, depressional‐basin wetland: forested swamps and herbaceous‐vegetation marshes. In west‐central Florida, >650 ML groundwater day^?1 are abstracted for use primarily in the Tampa Bay metropolis. At higher abstraction volumes, water tables were lower and wetlands had shorter hydroperiods (less time inundated). In turn, wetlands with shorter hydroperiods had 50–60% less SOM, C, and N per kg soil. In swamps, SOM loss caused soil bulk density to double, so areal soil C and N storage per m² through 30.5 cm depth was diminished by 25–30% in short‐hydroperiod swamps. In herbaceous‐vegetation marshes, short hydroperiods caused a sharper decline in N than in C. Soil organic matter, C, and N pools were not correlated with soil texture or with wetland draining‐reflooding frequency. Many years of shortened hydroperiod were probably required to diminish soil organic matter, C, and N pools by the magnitudes we observed. This diminution might have occurred decades ago, but could be maintained contemporarily by the failure each year of chronically drained soils to retain new organic matter inputs. In sum, our study attributes the contraction of hydroperiod and loss of soil organic matter, C, and N from rural wetlands to groundwater abstraction performed largely for urban water supply, revealing teleconnections between rural ecosystem change and urban resource demand.     

Annual burning of a tallgrass prairie inhibits C and N cycling in soil,increasing recalcitrant pyrogenic organic matter storage while reducing N availability

Grassland ecosystems store an estimated 30% of the world's total soil C and are frequently disturbed by wildfires or fire management. Aboveground litter decomposition is one of the main processes that form soil organic matter (SOM). However, during a fire biomass is removed or partially combusted and litter inputs to the soil are substituted with inputs of pyrogenic organic matter (py‐OM). Py‐OM accounts for a more recalcitrant plant input to SOM than fresh litter, and the historical frequency of burning may alter C and N retention of both fresh litter and py‐OM inputs to the soil. We compared the fate of these two forms of plant material by incubating ¹³C‐ and ¹⁵N‐labeled Andropogon gerardii litter and py‐OM at both an annually burned and an infrequently burned tallgrass prairie site for 11 months. We traced litter and py‐OM C and N into uncomplexed and organo‐mineral SOM fractions and CO₂ fluxes and determined how fire history affects the fate of these two forms of aboveground biomass. Evidence from CO₂ fluxes and SOM C:N ratios indicates that the litter was microbially transformed during decomposition while, besides an initial labile fraction, py‐OM added to SOM largely untransformed by soil microbes. Additionally, at the N‐limited annually burned site, litter N was tightly conserved. Together, these results demonstrate how, although py‐OM may contribute to C and N sequestration in the soil due to its resistance to microbial degradation, a long history of annual removal of fresh litter and input of py‐OM infers N limitation due to the inhibition of microbial decomposition of aboveground plant inputs to the soil. These results provide new insight into how fire may impact plant inputs to the soil, and the effects of py‐OM on SOM formation and ecosystem C and N cycling.     

5300-Year-old soil carbon is less primed than young soil organic matter

Soils harbor more than three times as much carbon (C) as the atmosphere, a large fraction of which (stable organic matter) serves as the most important global C reservoir due to its long residence time. Litter and root inputs bring fresh organic matter (FOM) into the soil and accelerate the turnover of stable C pools, and this phenomenon is termed the “priming effect” (PE). Compared with knowledge about labile soil C pools, very little is known about the vulnerability of stable C to priming. Using two soils that substantially differed in age (500 and 5300 years before present) and in the degree of chemical recalcitrance and physical protection of soil organic matter (SOM), we showed that leaf litter amendment primed 264% more organic C from the young SOM than from the old soil with very stable C. Hierarchical partitioning analysis confirmed that SOM stability, reflected mainly by available C and aggregate protection of SOM, is the most important predictor of leaf litter-induced PE. The addition of complex FOM (i.e., leaf litter) caused a higher bacterial oligotroph/copiotroph (K-/r-strategists) ratio, leading to a PE that was 583% and 126% greater than when simple FOM (i.e., glucose) was added to the young and old soils, respectively. This implies that the PE intensity depends on the chemical similarity between the primer (here FOM) and SOM. Nitrogen (N) mining existed when N and simple FOM were added (i.e., Glucose+N), and N addition raised the leaf litter-induced PE in the old soil that had low N availability, which was well explained by the microbial stoichiometry. In conclusion, the PE induced by FOM inputs strongly decreases with increasing SOM stability. However, the contribution of stable SOM to CO₂ efflux cannot be disregarded due to its huge pool size.     

Paired-tower measurements of carbon and energy fluxes following disturbance in the boreal forest

Disturbances by fire and harvesting are thought to regulate the carbon balance of the Canadian boreal forest over scales of several decades. However, there are few direct measurements of carbon fluxes following disturbances to provide data needed to refine mathematical models. The eddy covariance technique was used with paired towers to measure fluxes simultaneously at disturbed and undisturbed sites over periods of about one week during the growing season in 1998 and 1999. Comparisons were conducted at three sites: a 1‐y‐old burned jackpine stand subjected to an intense crown fire at the International Crown Fire Modelling Experiment site near Fort Providence, North‐west Territories; a 1‐y‐old clearcut aspen area at the EMEND project near Peace River, Alberta; and a 10‐y‐old burned, mixed forest near Prince Albert National Park, Saskatchewan. Nearby mature forest stands of the same types were also measured as controls. The harvested site had lower net radiation (R_n), sensible (H) and latent (LE) heat fluxes, and greater ground heat fluxes (G) than the mature forest. Daytime CO₂ fluxes were much reduced, but night‐time CO₂ fluxes were identical to that of the mature aspen forest. It is hypothesized that the aspen roots remained alive following harvesting, and dominated soil respiration. The overall effect was that the harvested site was a carbon source of about 1.6 gC m^?2 day^?1, while the mature site was a sink of about ?3.8 gC m^?2 day^?1. The one‐year‐old burn had lower R_n, H and LE than the mature jackpine forest, and had a continuous CO₂ efflux of about 0.8 gC m^–2 day^?1 compared to the mature forest sink of ? 0.5 g C m^?2 day^?1. The carbon source was likely caused by decomposition of fire‐killed vegetation. The 10‐y‐old burned site had similar H, LE, and G to the mature mixed forest site. Although the diurnal amplitude of the CO₂ fluxes were slightly lower at the 10‐y‐old site, there was no significant difference between the daily integrals (? 1.3 gC m^?2 day^?1 at both sites). It appears that most of the change in carbon flux occurs within the first 10 years following disturbance, but more data are needed on other forest and disturbance types for the first 20 years following the disturbance event.     

Impact of afforestation-associated management changes on the carbon balance of grassland

Afforestations can be considerable carbon (C) sources due to C losses from the soil after site preparation for tree planting and decreased primary production. In this study, the transition from grassland to afforestation was investigated using two eddy flux towers, which were operated in parallel for 3 years, one on a young afforestation and one on an adjacent grassland. Differences between the fluxes at the two sites were attributable to the management of the sites, without confounding influences of meteorological variability. Site preparation with deep ploughing of the planting rows destroyed 30% of the grassland vegetation at the afforestation site and reduced gross primary productivity by 41% in the first year. At the afforestation site 38 g m^?2 less C was sequestered compared with the nonafforested grassland during the first year. In the following years, the C sink at the afforestation site was higher than at the grassland indicating that soil C loss due to site preparation and land use change on the afforestation occurred only during the first year. Metrological conditions, especially summer drought, caused a high interannual variability of the C balance: both sites were small C sources in 2005 (67 g C m^?2 a^?1 at the grassland and 19 g C g^?1 a^?1 at the afforestation site) and small C sinks in 2004 and 2006 (?72.5 and ?16 g C m^?2 a^?1 at the grassland and ?34 and ?61 g C g^?1 a^?1 at the afforestation). Sheep grazing and mowing affected the short‐term dynamics of the C balance and sheep grazing accelerated the C turnover on the grassland site. The investigated afforestation site did not provide any short‐term way of sequestering additional C even though soil C losses during the first 3 years were relatively small.     

Land-Use Intensity Effects on Soil Organic Carbon Accumulation Rates and Mechanisms

Restoring soil C pools by reducing land use intensity is a potentially high impact, rapidly deployable strategy for partially offsetting atmospheric CO₂ increases. However, rates of C accumulation and underlying mechanisms have rarely been determined for a range of managed and successional ecosystems on the same soil type. We determined soil organic matter (SOM) fractions with the highest potential for sequestering C in ten ecosystems on the same soil series using both density- and incubation-based fractionation methods. Ecosystems included four annual row-crop systems (conventional, low input, organic and no-till), two perennial cropping systems (alfalfa and poplar), and four native ecosystems (early successional, midsuccessional historically tilled, midsuccessional never-tilled, and late successional forest). Enhanced C storage to 5 cm relative to conventional agriculture ranged from 8.9 g C m⁻² y⁻¹ in low input row crops to 31.6 g C m⁻² y⁻¹ in the early successional ecosystem. Carbon sequestration across all ecosystems occurred in aggregate-associated pools larger than 53 μm. The density-based fractionation scheme identified heavy-fraction C pools (SOM > 1.6 g cm⁻³ plus SOM < 53 μm), particularly those in macroaggregates (>250 μm), as having the highest potential C accumulation rates, ranging from 8.79 g C m⁻² y⁻¹ in low input row crops to 29.22 g C m⁻² y⁻¹ in the alfalfa ecosystem. Intra-aggregate light fraction pools accumulated C at slower rates, but generally faster than in inter-aggregate LF pools. Incubation-based methods that fractionated soil into active, slow and passive pools showed that C accumulated primarily in slow and resistant pools. However, crushing aggregates in a manner that simulates tillage resulted in a substantial transfer of C from slow pools with field mean residence times of decades to active pools with mean residence times of only weeks. Our results demonstrate that soil C accumulates almost entirely in soil aggregates, mostly in macroaggregates, following reductions in land use intensity. The potentially rapid destruction of macroaggregates following tillage, however, raises concerns about the long-term persistence of these C pools.     

Shrub expansion stimulates soil C and N storage along a coastal soil chronosequence

Expansion of woody vegetation in grasslands is a worldwide phenomenon with implications for C and N cycling at local, regional and global scales. Although woody encroachment is often accompanied by increased annual net primary production (ANPP) and increased inputs of litter, mesic ecosystems may become sources for C after woody encroachment because stimulation of soil CO₂ efflux releases stored soil carbon. Our objective was to determine if young, sandy soils on a barrier island became a sink for C after encroachment of the nitrogen‐fixing shrub Morella cerifera, or if associated stimulation of soil CO₂ efflux mitigated increased litterfall. We monitored variations in litterfall in shrub thickets across a chronosequence of shrub expansion and compared those data to previous measurements of ANPP in adjacent grasslands. In the final year, we quantified standing litter C and N pools in shrub thickets and soil organic matter (SOM), soil organic carbon (SOC), soil total nitrogen (TN) and soil CO₂ efflux in shrub thickets and adjacent grasslands. Heavy litterfall resulted in a dense litter layer storing an average of 809 g C m^?2 and 36 g N m^?2. Although soil CO₂ efflux was stimulated by shrub encroachment in younger soils, soil CO₂ efflux did not vary between shrub thickets and grasslands in the oldest soils and increases in CO₂ efflux in shrub thickets did not offset contributions of increased litterfall to SOC. SOC was 3.6–9.8 times higher beneath shrub thickets than in grassland soils and soil TN was 2.5–7.7 times higher under shrub thickets. Accumulation rates of soil and litter C were highest in the youngest thicket at 101 g m^?2 yr^?1 and declined with increasing thicket age. Expansion of shrubs on barrier islands, which have low levels of soil carbon and high potential for ANPP, has the potential to significantly increase ecosystem C sequestration.