The catchment and climate regulation of pCO2 in boreal lakes

The regulation of surface water pCO₂ was studied in a set of 33 unproductive boreal lakes of different humic content, situated along a latitudinal gradient (57°N to 64°N) in Sweden. The lakes were sampled four times during one year, and analyzed on a wide variety of water chemistry parameters. With only one exception, all lakes were supersaturated with CO₂ with respect to the atmosphere at all sampling occasions. pCO₂ was closely related to the DOC concentration in lakes, which in turn was mainly regulated by catchment characteristics. This pattern was similar along the latitudinal gradient and at different seasons of the year, indicating that it is valid for a variety of climatic conditions within the boreal forest zone. We suggest that landscape characteristics determine the accumulation and subsequent supply of allochthonous organic matter from boreal catchments to lakes, which in turn results in boreal lakes becoming net sources of atmospheric CO₂.     

Role of lakes for organic carbon cycling in the boreal zone

We calculated the carbon loss (mineralization plus sedimentation) and net CO₂ escape to the atmosphere for 79 536 lakes and total running water in 21 major Scandinavian catchments (size range 437–48 263 km²). Between 30% and 80% of the total organic carbon that entered the freshwater ecosystems was lost in lakes. Mineralization in lakes and subsequent CO₂ emission to the atmosphere was by far the most important carbon loss process. The withdrawal capacity of lakes on the catchment scale was closely correlated to the mean residence time of surface water in the catchment, and to some extent to the annual mean temperature represented by latitude. This result implies that variation of the hydrology can be a more important determinant of CO₂ emission from lakes than temperature fluctuations. Mineralization of terrestrially derived organic carbon in lakes is an important regulator of organic carbon export to the sea and may affect the net exchange of CO₂ between the atmosphere and the boreal landscape.     

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.     

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.     

The disappearance of relict permafrost in boreal north America: Effects on peatland carbon storage and fluxes

Boreal peatlands in Canada have harbored relict permafrost since the Little Ice Age due to the strong insulating properties of peat. Ongoing climate change has triggered widespread degradation of localized permafrost in peatlands across continental Canada. Here, we explore the influence of differing permafrost regimes (bogs with no surface permafrost, localized permafrost features with surface permafrost, and internal lawns representing areas of permafrost degradation) on rates of peat accumulation at the southernmost limit of permafrost in continental Canada. Net organic matter accumulation generally was greater in unfrozen bogs and internal lawns than in the permafrost landforms, suggesting that surface permafrost inhibits peat accumulation and that degradation of surface permafrost stimulates net carbon storage in peatlands. To determine whether differences in substrate quality across permafrost regimes control trace gas emissions to the atmosphere, we used a reciprocal transplant study to experimentally evaluate environmental versus substrate controls on carbon emissions from bog, internal lawn, and permafrost peat. Emissions of CO₂ were highest from peat incubated in the localized permafrost feature, suggesting that slow organic matter accumulation rates are due, at least in part, to rapid decomposition in surface permafrost peat. Emissions of CH₄ were greatest from peat incubated in the internal lawn, regardless of peat type. Localized permafrost features in peatlands represent relict surface permafrost in disequilibrium with the current climate of boreal North America, and therefore are extremely sensitive to ongoing and future climate change. Our results suggest that the loss of surface permafrost in peatlands increases net carbon storage as peat, though in terms of radiative forcing, increased CH₄ emissions to the atmosphere will partially or even completely offset this enhanced peatland carbon sink for at least 70 years following permafrost degradation.     

森林生态系统可溶性碳和颗粒碳通量

可溶性碳(Dissolved carbon,DC)和颗粒碳(particulate carbon,PC)通量作为森林生态系统碳收支的重要组分,在森林固碳功能的评价和模型预测中具有重要意义,但常因认识不足、测定困难等而在森林碳汇研究中被忽略。综述了森林生态系统DC和PC的组成、作用、相关生态过程及其影响因子,并展望了该领域应该优先考虑的研究问题。森林生态系统DC和PC主要包括可溶性有机碳、可溶性无机碳和颗粒有机碳,主要来源于生态系统的净初级生产量。DC和PC是森林土壤的活性碳库,主要以大气沉降、穿透雨和凋落物的形式输入森林土壤系统,并通过土壤呼吸、侧向运输及渗透流失的方式输出生态系统。从局域尺度看,DC和PC通量受根系分泌、细根分解、微生物周转等生物过程的影响较大;从区域尺度看,它们受土壤和植被特性、生态过程耦联关系、气候因子以及全球变化的综合影响。该领域应该优先考虑:(1)探索不同时空尺度下森林生态系统DC和PC通量的控制因子及其耦联关系,揭示其中的驱动机理;(2)探索DC和PC与其它森林生态系统碳组分的相互关系及转化,阐明DC和PC通量与其它养分之间潜在的生态化学计量关系;(3)探索全球变化,特别是人类活动(如森林经营)和极端干扰事件(如林火、旱涝、冰冻、冻融交替等)对森林生态系统DC和PC通量的影响。     

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

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

Aquatic export of young dissolved and gaseous carbon from a pristine boreal fen: Implications for peat carbon stock stability

The stability of northern peatland's carbon (C) store under changing climate is of major concern for the global C cycle. The aquatic export of C from boreal peatlands is recognized as both a critical pathway for the remobilization of peat C stocks as well as a major component of the net ecosystem C balance (NECB). Here, we present a full year characterization of radiocarbon content (¹⁴C) of dissolved organic carbon (DOC), carbon dioxide (CO₂), and methane (CH₄) exported from a boreal peatland catchment coupled with ¹⁴C characterization of the catchment's peat profile of the same C species. The age of aquatic C in runoff varied little throughout the year and appeared to be sustained by recently fixed C from the atmosphere (<60 years), despite stream DOC, CO₂, and CH₄ primarily being sourced from deep peat horizons (2–4 m) near the mire's outlet. In fact, the ¹⁴C content of DOC, CO₂, and CH₄ across the entire peat profile was considerably enriched with postbomb C compared with the solid peat material. Overall, our results demonstrate little to no mobilization of ancient C stocks from this boreal peatland and a relatively large resilience of the source of aquatic C export to forecasted hydroclimatic changes.     

Mineralisation of dissolved organic matter by heterotrophic stream biofilm communities in a large boreal catchment

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北方森林土壤呼吸和木质残体分解释放出的CO2通量

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Carbon uptake in Eurasian boreal forests dominates the high-latitude net ecosystem carbon budget

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A stable carbon isotope study of dissolved inorganic carbon cycling in a softwater lake

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青藏高原高寒草原碳排放及其迁移过程研究

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Linking forest fires to lake metabolism and carbon dioxide emissions in the boreal region of Northern Québec

Natural fires annually decimate up to 1% of the forested area in the boreal region of Québec, and represent a major structuring force in the region, creating a mosaic of watersheds characterized by large variations in vegetation structure and composition. Here, we investigate the possible connections between this fire‐induced watershed heterogeneity and lake metabolism and CO₂ dynamics. Plankton respiration, and water–air CO₂ fluxes were measured in the epilimnia of 50 lakes, selected to lie within distinct watershed types in terms of postfire terrestrial succession in the boreal region of Northern Québec. Plankton respiration varied widely among lakes (from 21 to 211 μg C L^?1 day^?1), was negatively related to lake area, and positively related to dissolved organic carbon (DOC). All lakes were supersaturated in CO₂ and the resulting carbon (C) flux to the atmosphere (150 to over 3000 mg C m² day^?1) was negatively related to lake area and positively to DOC concentration. CO₂ fluxes were positively related to integrated water column respiration, suggesting a biological component in this flux. Both respiration and CO₂ fluxes were strongly negatively related to years after the last fire in the basin, such that lakes in recently burnt basins had significantly higher C emissions, even after the influence of lake size was removed. No significant differences were found in nutrients, chlorophyll, and DOC between lakes in different basin types, suggesting that the fire‐induced watershed features influence other, more subtle aspects, such as the quality of the organic C reaching lakes. The fire‐induced enhancement of lake organic C mineralization and C emissions represents a long‐term impact that increases the overall C loss from the landscape as the result of fire, but which has never been included in current regional C budgets and future projections. The need to account for this additional fire‐induced C loss becomes critical in the face of predictions of increasing incidence of fire in the circumboreal landscape.     

Concentration and composition of dissolved organic carbon in streams in relation to catchment soil properties

Two adjacent catchments in the Otway Ranges of Victoria, Australia (Redwater and Clearwater) produce water with markedly different concentrations of dissolved organic carbon (DOC) during summer. Water from Redwater Creek had a DOC concentration of 32 mg L^–1, while water from Clearwater Creek had a DOC concentration of 3.8 mg L^–1. Examination of the catchments revealed that while climate, topography, vegetation and land use were similar, the soils were different. The objective of this study was to examine the relationship between the concentration and chemical composition of DOC in stream waters and the nature of soils in the two catchments. Soil mapping determined that clayey soils formed on Cretaceous sediments (Cretaceous soils) occurred throughout both catchments, but that Redwater Catchment also contained a large area (39%) of sandy soils formed on Tertiary sediments (Tertiary soils). The concentration of DOC in forest floor leachate was high in both the Tertiary and Cretaceous areas; however, the concentration of DOC in water draining areas dominated by Tertiary soils was greater than that in water draining areas dominated by Cretaceous soils. Laboratory experiments showed that the Cretaceous soils had higher adsorption capacities for forest floor leachate DOC than the Tertiary soils. The difference in DOC concentrations of the streams was therefore attributed to the difference in adsorption capacity of catchment soils for DOC. Adsorption capacities of the soils were found to be a function of their clay contents and specific surface areas.Solid-state³C nuclear magnetic resonance spectroscopy and pyrolysis-mass spectrometry were used to determine the chemical structure of DOC found in streams and forest floor leachate samples and that remaining in solution after interaction with soil. Chemistry of DOC in forest floor leachate was similar before and after interaction with soil, indicating no preferential adsorption of a particular type of carbon. Thus, differences between the chemical structure of stream DOC and forest floor leachate DOC could be attributed to microbial modifications during its movement through soils and into the streams, rather than losses by adsorption.     

The Net Landscape Carbon Balance—Integrating terrestrial and aquatic carbon fluxes in a managed boreal forest landscape in Sweden

The boreal biome exchanges large amounts of carbon (C) and greenhouse gases (GHGs) with the atmosphere and thus significantly affects the global climate. A managed boreal landscape consists of various sinks and sources of carbon dioxide (CO₂), methane (CH₄), and dissolved organic and inorganic carbon (DOC and DIC) across forests, mires, lakes, and streams. Due to the spatial heterogeneity, large uncertainties exist regarding the net landscape carbon balance (NLCB). In this study, we compiled terrestrial and aquatic fluxes of CO₂, CH₄, DOC, DIC, and harvested C obtained from tall‐tower eddy covariance measurements, stream monitoring, and remote sensing of biomass stocks for an entire boreal catchment (~68 km²) in Sweden to estimate the NLCB across the land–water–atmosphere continuum. Our results showed that this managed boreal forest landscape was a net C sink (NLCB = 39 g C m^?2 year^?1) with the landscape–atmosphere CO₂ exchange being the dominant component, followed by the C export via harvest and streams. Accounting for the global warming potential of CH₄, the landscape was a GHG sink of 237 g CO₂‐eq m^?2 year^?1, thus providing a climate‐cooling effect. The CH₄ flux contribution to the annual GHG budget increased from 0.6% during spring to 3.2% during winter. The aquatic C loss was most significant during spring contributing 8% to the annual NLCB. We further found that abiotic controls (e.g., air temperature and incoming radiation) regulated the temporal variability of the NLCB whereas land cover types (e.g., mire vs. forest) and management practices (e.g., clear‐cutting) determined their spatial variability. Our study advocates the need for integrating terrestrial and aquatic fluxes at the landscape scale based on tall‐tower eddy covariance measurements combined with biomass stock and stream monitoring to develop a holistic understanding of the NLCB of managed boreal forest landscapes and to better evaluate their potential for mitigating climate change.     

Sources and sinks of dissolved organic carbon in a forested swamp catchment

Concentrations of dissolved organic carbon (DOC) were measured in precipitation, throughfall, stemflow, and soil, peat and stream water in a 50 ha catchment with a central 5 ha swamp at Mont St. Hilaire, Quebec. DOC concentrations in precipitation were low (2.0 mg L^–1), but increased in passage through the tree canopies as throughfall (9.1–14.6 mg L^–1) and stemflow (23.1–30.1 mg L^–1). For the period July 1–November 15, 1987, 0.5 g DOC m^–2 was imported as precipitation, and forest canopies contributed a further 1.4–1.7 g m^–2 2 to the soil surface. DOC concentrations were higher (46.0 and 67.6 mg L^–1) in upland soil organic horizons, but decreased with depth because subsoil mineral horizons acted as a major sink of DOC. A laboratory experiment using leaf leachate revealed that subsoil horizons were able to adsorb DOC, with equilibrium DOC concentrations ranging from 3 to 19 mg L^–1. Soil organic carbon appeared to be an important determinant of equilibrium DOC concentrations. The swamp was a major source of DOC, with an overall average DOC concentration of 58.6 mg L^–1 and showed strong spatial and temporal variations related to hydrologic and thermal regimes. During base flow periods, stream DOC concentrations were small (< 3 mg L^–1), dominated by water fed from springs draining upland soils. During high flows, stream DOC concentrations increased through the contribution of DOC-rich water originating in the swamp. Sources, sinks and transport of DOC are thus a function of a complex set of inter-related biotic and abiotic process.     

Closing the carbon budget of estuarine wetlands with tower-based measurements and MODIS time series

Compared to other ecosystems, estuarine ecosystems have distinct carbon flux dynamics – the lateral carbon flux incurred by tidal activities, and methane generation under the anaerobic conditions of wetland soils. The conventional estimation of gross primary production (GPP) based on the light use efficiency (LUE) model used for non‐wetland terrestrial ecosystems, therefore, cannot be applied directly to estuarine wetland ecosystems. In this paper, we estimated the 2005's annual carbon budget of an estuarine wetland on Chongming Island, Shanghai, and partitioned the losses of carbon due to lateral tidal dynamics and anaerobic methane production using an innovative technique. The average GPP calculated from eddy covariance between March and November was 261.79 μmol m^?2 day^?1, whereas that from the LUE model was 58.84 μmol m^?2 day^?1. The correlation coefficient between GPP simulated from the LUE model and that calculated from flux tower data was low in the growing season (R²=0.55). We hypothesized that tidal activities and uncounted methane release were responsible for the difference, which can be predicted from measurements of remote sensing products such as land surface water index (LSWI), evapotranspiration (ET), and tide height (TH). We developed an integrated GPP model by combining the LUE model and an autoregression model to estimate carbon budget. The average GPP from the modified model increased to 263.38 μmol m^?2 day^?1, and R² for the correlation between the simulated and calculated data increased to 0.88, demonstrating the potential of our technique for GPP estimation and quantification of seasonal variation in estuarine ecosystems. The approach developed in this study has great potential for correcting unavoidable errors when estimating carbon budget of coastal wetlands. Furthermore, global warming is expected to accelerate sea level rise, which may enhance the effect of tidal activities and increase the difficulty in estimating coastal carbon budgets using conventional methods.     

Effects of increased CO2 and N on CH4 efflux from a boreal mire: a growth chamber experiment

Increases in the supply of atmospheric CO₂ and N are expected to alter the carbon cycle, including CH₄ emissions, in boreal peatlands. These effects were studied in a glasshouse experiment with peat monoliths cored from an oligotrophic pine fen. The cores with living plants were kept in 720 ppm_v and 360 ppm_v CO₂ atmospheres for about 6 months under imitated natural temperature cycle. Fertilisation with NH₄NO₃ (3 g m⁻² for 25 weeks) was applied to 18 of the 36 monoliths. The rate of CH₄ flux was non-linearly dependent on the number of Eriophorum vaginatum shoots growing in the monoliths, probably due to the gas transport properties of the aerenchyma. The average CH₄ efflux rate, standardised by the number of shoots, was increased by a maximum of 10–20% in response to the raised CO₂ level. In the raised-NH₄NO₃ treatment, the increase in CH₄ release was lower. The effect of combined CO₂+NH₄NO₃ on CH₄ release was negligible and even lower than in the single treatments. Both potential CH₄ production and oxidation rates at 5, 15 and 25°C were higher near the surface than at the bottom of the core. As expected, the rates clearly depended on the incubation temperature, but the different treatments did not cause any consistent differences in either CH₄ production or oxidation. The determination of potential CH₄ production and oxidation in the laboratory is evidently too crude a method of differentiating substrate-induced differences in CH₄ production and oxidation in vivo. These results indicate that an increase in atmospheric CO₂ or N supply alone, at least in the short term, slightly enhances CH₄ effluxes from boreal peatlands; but together their effect may even be restrictive. Received: 18 June 1998 / Accepted: 25 January 1999