CO<Subscript>2</Subscript> Air–Sea Exchange due to Calcium Carbonate and Organic Matter Storage,and its Implications for the Global Carbon Cycle

Release of CO₂ from surface ocean water owing to precipitation of CaCO₃ and the imbalance between biological production of organic matter and its respiration, and their net removal from surface water to sedimentary storage was studied by means of a quotient θ = (CO₂ flux to the atmosphere)/(CaCO₃ precipitated). θ depends not only on water temperature and atmospheric CO₂ concentration but also on the CaCO₃ and organic carbon masses formed. In CO₂ generation by CaCO₃ precipitation, θ varies from a fraction of 0.44 to 0.79, increasing with decreasing temperature (25 to 5°C), increasing atmospheric CO₂ concentration (195–375 ppmv), and increasing CaCO₃ precipitated mass (up to 45% of the initial DIC concentration in surface water). Primary production and net storage of organic carbon counteracts the CO₂ production by carbonate precipitation and it results in lower CO₂ emissions from the surface layer. When atmospheric CO₂ increases due to the ocean-to-atmosphere flux rather than remaining constant, the amount of CO₂ transferred is a non-linear function of the surface layer thickness because of the back-pressure of the rising atmospheric CO₂. For a surface ocean layer approximated by a 50-m-thick euphotic zone that receives input of inorganic and organic carbon from land, the calculated CO₂ flux to the atmosphere is a function of the CaCO₃ and C_org net storage rates. In general, the carbonate storage rate has been greater than that of organic carbon. The CO₂ flux near the Last Glacial Maximum is 17 to 7×10¹² mol/yr (0.2–0.08 Gt C/yr), reflecting the range of organic carbon storage rates in sediments, and for pre-industrial time it is 38–42×10¹² mol/yr (0.46–0.50 Gt C/yr). Within the imbalanced global carbon cycle, our estimates indicate that prior to anthropogenic emissions of CO₂ to the atmosphere the land organic reservoir was gaining carbon and the surface ocean was losing carbon, calcium, and total alkalinity owing to the CaCO₃ storage and consequent emission of CO₂. These results are in agreement with the conclusions of a number of other investigators. As the CO₂ uptake in mineral weathering is a major flux in the global carbon cycle, the CO₂ weathering pathway that originates in the CO₂ produced by remineralization of soil humus rather than by direct uptake from the atmosphere may reduce the relatively large imbalances of the atmosphere and land organic reservoir at 10²–10⁴-year time scales.     

Modern carbon burial in Lake Qinghai,China

The quantification of carbon burial in lake sediments, and carbon fluxes derived from different origins are crucial to understand modern lacustrine carbon budgets, and to assess the role of lakes in the global carbon cycle. In this study, we estimated carbon burial in the sediment of Lake Qinghai, the largest inland lake in China, and the carbon fluxes derived from different origins. We find that: (1) The organic carbon burial rate in lake sediment is approximately 7.23 g m⁻² a⁻¹, which is comparable to rates documented in many large lakes worldwide. We determined that the flux of riverine particulate organic carbon (POC) is approximately 10 times higher than that of dissolved organic carbon (DOC). Organic matter in lake sediments is primarily derived from POC in lake water, of which approximately 80% is of terrestrial origin. (2) The inorganic carbon burial rate in lake sediment is slightly higher than that of organic carbon. The flux of riverine dissolved inorganic carbon (DIC) is approximately 20 times that of DOC, and more than 70% of the riverine DIC is drawn directly and/or indirectly from atmospheric CO₂. (3) Both DIC and DOC are concentrated in lake water, suggesting that the lake serves as a sink for both organic and inorganic carbon over long term timescales. (4) Our analysis suggests that the carbon burial rates in Lake Qinghai would be much higher in warmer climatic periods than in cold ones, implying a growing role in the global carbon cycle under a continued global warming scenario.     

全球变化条件下的土壤呼吸效应

土壤呼吸是陆地植物固定CO₂尔后又释放CO₂返回大气的主要途径，是与全球变化有关的一个重要过程。综述了全球变化下CO₂浓度上升、全球增温、耕作方式的改变及氮沉降增加的土壤呼吸效应。大气CO₂浓度的上升将增加土壤中CO₂的释放通量，同时将促进土壤的碳吸存；在全球增温的情形下，土壤可能向大气中释放更多的CO₂，传统的土地利用方式可能是引发温室气体CO₂产生的重要原因，所有这些全球变化对土壤呼吸的作用具有不确定性。认为土壤碳库的碳储量增加并不能减缓21世纪大气CO₂浓度的上升。据此讨论了该问题的对策并提出了今后土壤呼吸的一些研究方向。其中强调，尽管森林土壤碳固定能力有限，但植树造林、森林保护是一项缓解大气CO₂上升的可行性对策；基于现有田间尺度CO₂通量测定在不确定性方面的进展，今后应继续朝大尺度田间和模拟程序方面努力；着重回答全球变化条件下的土壤呼吸过程机理；区分土壤呼吸的不同来源以及弄清土壤呼吸黑箱系统中土壤微生物及土壤动物的功能。当然，土壤呼吸的测定方法尚有待改善。     

Effects of short-term ecosystem experimental warming on water-extractable organic matter in an ombrotrophic Sphagnum peatland (Le Forbonnet, France)

In a future warmer world, peatlands may change from a carbon sink function to a carbon source function. This study tracks changes in water-extractable organic matter (WEOM) after 1 year of in situ experimental warming using open top chambers (OTCs). WEOM was studied in the upper peat layers (0–10 cm) through analysis of water-extractable organic carbon (WEOC), stable C isotopic composition (δ¹³C), specific UV absorbance at 280 nm and sugar composition of cores taken from an open bog (DRY sites) and a transitional poor fen (WET sites). At the DRY sites, the impact of OTCs was weak with respect to WEOM parameters, whereas at the WET sites, the air warming treatment led to a decrease in peat water content, suggesting that the supply of heat by OTCs was used mainly for evapotranspiration. OTCs at the WET sites also induced a relative enrichment at the surface (0–5 cm depth) of aliphatic and/or aromatic compounds with concomitant decrease in WEOC, as a result of decomposition. On the contrary, WEOC and sugar content increased in the deeper peat layer (7.5–10 cm depth) probably as a result of increased leaching of phenolic compounds by roots, which then inhibits microbial activity. The different response to experimental warming at DRY and WET sites suggests that the spatial variability of moisture is critical for understanding of the impact of global warming on the fate of OM and the carbon cycle in peatlands.     

CO<Subscript>2</Subscript> absorption by alkaline soils and its implication to the global carbon cycle

Motivated by the rapid increase in atmospheric CO₂ due to human activities since the Industrial Revolution, and the climate changes it produced, the world’s concerned scientific community has made a huge effort to investigate the global carbon cycle. However, the results reveal that the global CO₂ budget cannot be balanced, unless a “missing sink” is invoked. Although numerous studies claimed to find the “missing sink”, none of those claims has been widely accepted. This current study showed that alkaline soil on land are absorbing CO₂ at a rate of 0.3–3.0 μmol m⁻² s⁻¹ with an inorganic, non-biological process. The intensity of this CO₂ absorption is determined by the salinity, alkalinity, temperature and water content of the saline/alkaline soils, which are widely distributed on land. Further studies revealed that high salinity or alkalinity positively affected the CO₂ absorbing intensity, while high temperature and water content had a negative effect on the CO₂ absorbing intensity of these soils. This inorganic, non-biological process of CO₂ absorption by alkaline soils might have significant implications to the global carbon budget accounting.     

Holocene carbon storage and testate amoeba community structure in treed peatlands of the western Hudson Bay Lowlands margin,Canada

The Hudson Bay Lowlands (HBL) stores a significant proportion of the northern peatland carbon pool, and constraints on the factors controlling local-scale variation are needed to better predict soil carbon stocks. We investigated two treed peatland sites, a fen and a bog, to understand how local ecohydrological factors impacted long-term carbon storage. Ecohydrological conditions were reconstructed using quantitative water table depth reconstructions from testate amoebae (TA) and broad peat type classifications. We also linked these factors and carbon storage to changes in TA community structure through the investigation of morphological and functional traits. Both sites have high rates of peat vertical accretion during the warmer Middle Holocene. A shift to a drier, Sphagnum-dominated habitat after 7400 cal a bp at the bog site, however, led to lower apparent carbon accumulation rates (aCARs) than at the fen site. aCARs decreased with the transition to a cooler Late Holocene climate at both sites. Both sites have higher total carbon masses (kg m⁻²) than other more open and younger HBL localities, demonstrating the potential importance of treed peatlands in regional carbon storage. Shifts in the frequency of TA traits corresponded to changing ecohydrological conditions and provided insights into the role of TA in carbon storage.     

Diffusion and mass flow of dissolved carbon dioxide, methane, and dissolved organic carbon in a 7-m deep raised peat bog

In 65 samples, we got values (unusually replicable and consistent for this type of work) of concentration, ¹⁴C/¹³C (AMS) age, and δ¹³C for: peat, dissolved organic carbon (DOC), peat fractions, and dissolved CO₂ and CH₄ at 50-cm intervals down to 700 cm in Ellergower Moss, a rainwater-dependent raised (domed) bog in southwest Scotland. (1) We attribute the consistency of the results to Ellergower Moss being unusually homogeneous, with unusually low hydraulic conductivity, and containing only a few gas spaces; and to the sampling methods including 18-month equilibration of in situ samplers. (2) The dissolved gas concentration depth profiles are convex and very similar to each other, though CO₂ is 5-10 times more concentrated than CH₄, while the profile of DOC is concave. (3) The age profile of peat is near linearly proportional to depth; that for DOC is about 500-1000 yr younger than the peat at the same depth; the dissolved gases are 500-4300 years younger than the peat. The age of the operational peat fractions humic acid and humin is similar to that of whole peat. (4) The δ¹³C profile for deep peat is almost constant; δ¹³C-CO₂ is more enriched than the peat (δ¹³C-CO₂ 35‰ more); δ¹³C-CH₄ is the same amount more depleted. Nearer the surface both dissolved gases become steadily more depleted, δ¹³C is about 20‰ less at the surface. (5) A simulation shows that mass flow can account for the concentration and age profiles of DOC, but for the gases diffusion and an additional source near the surface are needed as well, and diffusion accounts for over 99% of the dissolved gas movements. (6) The same processes must operate in other peatlands but the results for Ellergower should not be extrapolated uncritically to them.     

Quantifying the carbon source of pedogenic calcite veins in weathered limestone: implications for the terrestrial carbon cycle

The continent is the second largest carbon sink on Earth’s surface. With the diversification of vascular land plants in the late Paleozoic, terrestrial organic carbon burial is represented by massive coal formation, while the development of soil profiles would account for both organic and inorganic carbon burial. As compared with soil organic carbon, inorganic carbon burial, collectively known as the soil carbonate, would have a greater impact on the long-term carbon cycle. Soil carbonate would have multiple carbon sources, including dissolution of host calcareous rocks, dissolved inorganic carbon from freshwater, and oxidation of organic matter, but the host calcareous rock dissolution would not cause atmospheric CO₂ drawdown. Thus, to evaluate the potential effect of soil carbonate formation on the atmospheric pCO₂ level, different carbon sources of soil carbonate should be quantitatively differentiated. In this study, we analyzed the carbon and magnesium isotopes of pedogenic calcite veins developed in a heavily weathered outcrop, consisting of limestone of the early Paleogene Guanzhuang Group in North China. Based on the C and Mg isotope data, we developed a numerical model to quantify the carbon source of calcite veins. The modeling results indicate that 4–37 wt% of carbon in these calcite veins was derived from atmospheric CO₂. The low contribution from atmospheric CO₂ might be attributed to the host limestone that might have diluted the atmospheric CO₂ sink. Nevertheless, taking this value into consideration, it is estimated that soil carbonate formation would lower 1 ppm atmospheric CO₂ within 2000 years, i.e., soil carbonate alone would sequester all atmospheric CO₂ within 1 million years. Finally, our study suggests the C–Mg isotope system might be a better tool in quantifying the carbon source of soil carbonate.

     

Ecosystem-driven karst carbon cycle and carbon sink effects

It is recognized that karst processes are actively involved in the current global carbon cycle based on twenty years research, and the carbon sink occurred in karst processes is possibly an important part of “missing sink” in global carbon cycle. In this paper, an overview is given on karst carbon cycle research, and influence factors, formed carbon pools (background carbon sink) and sink increase potentials of current karst carbon cycle are analyzed. Carbonate weathering could contribute to the imbalance item (B_IM) and land use change item (E_LUC) in the global carbon cycle model, owing to its uptake of both atmospheric CO₂ (carbon sink effect) and CO₂ produced by soil respiration (carbon source reduction effect). Karst carbon sink includes inorganic carbon sink resulted from hydrogeochemical process and organic carbon sink generated by aquatic photosynthetic DIC conversion, forming relatively stable river (reservoir) water body or sediment carbon sink. The sizes of both sinks are controlled by terrestrial ecosystems and aquatic ecosystems, respectively. Desertification rehabilitation and carbon sequestration by aquatic plants are two effective ways to increase the carbon sink in karst area. It is estimated that the rate of carbon sink is at least 381 000 t CO₂/a with vegetation restoration and afforestation in southwest China karst area, while the annual organic carbon sink generated by aquatic photosynthesis is about 84 200 t C in the Pearl River Basin. The development of a soil CO₂ based model for assessment of regional dissolution intensity will help to improve the estimation accuracy of carbon sink increase and potential, thus provide a more clear and efficient karst sink increase scheme and pathway to achieve the goals of “double carbon”. With the deep investigation on karst carbon cycle, mechanism and carbon sink effect, and the improvement of watershed carbon sink measurement methods and regional sink increase evaluation approaches. Karst carbon sink is expected to be included in the list of atmospheric CO₂ sources/sinks of the global carbon budget in the near future.     

Revised 14C dating of ice wedge growth in interior Alaska (USA) to MIS 2 reveals cold paleoclimate and carbon recycling in ancient permafrost terrain

Establishing firm radiocarbon chronologies for Quaternary permafrost sequences remains a challenge because of the persistence of old carbon in younger deposits. To investigate carbon dynamics and establish ice wedge formation ages in Interior Alaska, we dated a late Pleistocene ice wedge, formerly assigned to Marine Isotope Stage (MIS) 3, and host sediments near Fairbanks, Alaska, with 24 radiocarbon analyses on wood, particulate organic carbon (POC), air-bubble CO₂, and dissolved organic carbon (DOC). Our new CO₂ and DOC ages are up to 11,170 yr younger than ice wedge POC ages, indicating that POC is detrital in origin. We conclude an ice wedge formation age between 28 and 22 cal ka BP during cold stadial conditions of MIS 2 and solar insolation minimum, possibly associated with Heinrich event 2 or the last glacial maximum. A DOC age for an ice lens in a thaw unconformity above the ice wedge returned a maximum age of 21,470 ± 200 cal yr BP. Our variable ¹⁴C data indicate recycling of older carbon in ancient permafrost terrain, resulting in radiocarbon ages significantly older than the period of ice-wedge activity. Release of ancient carbon with climatic warming will therefore affect the global ¹⁴C budget.     

Effect of elevated CO2 on carbon pools and fluxes in a brackish marsh

The effects of long-term exposure to elevated atmospheric CO₂ (ambient + 340 ppmv) on carbon cycling were investigated for two plant communities in a Chesapeake Bay brackish marsh, one dominated by the C₃ sedgeSchoenplectus americanus and the other by the C₄ grassSpartina patens. Elevated CO₂ resulted in a significant increase in porewater concentrations of DIC at 30 cm depth (p < 0.1). The CO₂ treatment also yielded increases in DOC (15 to 27%) and dissolved CH₄ (12–18%) in the C₃ marsh (means for several depths over the period of June 1998 and June 1999), but not at a significant level. Elevated CO₂ increased mean ecosystem emissions of CO₂ (34–393 g C m⁻² yr⁻¹) and CH₄ (0.21–0.40 g C m⁻² yr⁻¹) in the C₃ community, but the effects were only significant on certain dates. For example, CO₂ enrichment increased C export to the atmosphere in the C₃ community during one of two winter seasons measured (p = 0.09). In the C₄ community, gross photosynthesis responded relatively weakly to elevated CO₂ (18% increase, p > 0.1), and the concomitant effects on dissolved carbon concentrations, respiration, and CH₄ emissions were small or absent. We concluded that elevated CO₂ has the potential to increase dissolved inorganic carbon export to estuaries.     

Sources of dissolved organic carbon in forest soils: evidences from the differences of organic carbon concentration and isotope composition studies

There is considerable discussion and uncertainty in the literature regarding the importance of fresh litter versus older soil organic matter as sources of soil dissolved organic carbon (DOC) in forest floor. In this study, the differences of organic carbon concentration and stable isotope composition were analyzed under different background conditions to identify the origins of DOC in forest soil. The data show that there is no significant difference in SOC content between these collected soil samples (P > 0.05), but the litter-rich surface soils have relatively higher DOC concentration than the litter-lacking (P < 0.01) ones, and the δ ¹³C values of DOC (δ ¹³C_DOC) are closer to δ ¹³C of litter than δ ¹³C values of SOC (δ ¹³C_SOC). In the litter-lacking surface soil samples, the range of δ ¹³C_DOC is between δ ¹³C_SOC and δ ¹³C of dominant plant leaves. These results suggest that DOC mainly derive from litter in the litter-rich surface soil with, and the main path of DOC sources may change with surrounding conditions. In addition, δ ¹³C_SOC and δ ¹³C_DOC become more positive, and the absolute values of Δ (δ ¹³C_DOC − δ ¹³C_SOC) decrease with depth in the soil profiles, which indicate that the percentage of DOC below 5 cm, derived from degradation of humus, may increase with soil depth.     

Benthic fluxes and porewater concentration profiles of dissolved organic carbon in sediments from the North Carolina continental slope

Numerous studies of marine environments show that dissolved organic carbon (DOC) concentrations in sediments are typically tenfold higher than in the overlying water. Large concentration gradients near the sediment–water interface suggest that there may be a significant flux of organic carbon from sediments to the water column. Furthermore, accumulation of DOC in the porewater may influence the burial and preservation of organic matter by promoting geopolymerization and/or adsorption reactions. We measured DOC concentration profiles (for porewater collected by centrifugation and “sipping”) and benthic fluxes (with in situ and shipboard chambers) at two sites on the North Carolina continental slope to better understand the controls on porewater DOC concentrations and quantify sediment–water exchange rates. We also measured a suite of sediment properties (e.g., sediment accumulation and bioturbation rates, organic carbon content, and mineral surface area) that allow us to examine the relationship between porewater DOC concentrations and organic carbon preservation. Sediment depth-distributions of DOC from a downslope transect (300–1000 m water depth) follow a trend consistent with other porewater constituents (ΣCO₂ and SO₄²⁻) and a tracer of modern, fine-grained sediment (fallout Pu), suggesting that DOC levels are regulated by organic matter remineralization. However, remineralization rates appear to be relatively uniform across the sediment transect. A simple diagenetic model illustrates that variations in DOC profiles at this site may be due to differences in the depth of the active remineralization zone, which in turn is largely controlled by the intensity of bioturbation. Comparison of porewater DOC concentrations, organic carbon burial efficiency, and organic matter sorption suggest that DOC levels are not a major factor in promoting organic matter preservation or loading on grain surfaces. The DOC benthic fluxes are difficult to detect, but suggest that only 2% of the dissolved organic carbon escapes remineralization in the sediments by transport across the sediment-water interface.     

Assessment of soil carbon pool,carbon sequestration and soil CO<Subscript>2</Subscript> flux in unreclaimed and reclaimed coal mine spoils

Surface coal mining inevitably deforests the land, reduces carbon (C) pool and generates different land covers. To re-establish the ecosystem C pool, post-mining lands are often afforested with fast-growing trees. A field study was conducted in the 5-year-old unreclaimed dump and reclaimed coal mine dump to assess the changes in soil CO₂ flux and compared with the reference forest site. Changes in soil organic carbon (SOC) and total nitrogen stocks were estimated in post-mining land. Soil CO₂ flux was measured using close dynamic chamber method, and the influence of environmental variables on soil CO₂ flux was determined. Woody biomass C and SOC stocks of the reference forest site were threefold higher than that of 5-year-old reclaimed site. The mean soil CO₂ flux was highest in 5-year-old reclaimed dump (2.37 μmol CO₂ m^?2 s^?1) and lowest in unreclaimed dump (0.21 μmol CO₂ m^?2 s^?1). Soil CO₂ flux was highly influenced by environmental variables, where soil temperature positively influenced the soil CO₂ flux, while soil moisture, relative humidity and surface CO₂ concentration negatively influenced the soil CO₂ flux. Change in soil CO₂ flux under different land cover depends on plant and soil characteristics and environmental variables. The study concluded that assessment of soil CO₂ flux in post-mining land is important to estimate the potential of afforestation to combat increased emission of soil CO₂ at regional and global scale.     

Holocene development and permafrost history in sub‐arctic peatlands in Tavvavuoma,northern Sweden

Under changing climatic conditions permafrost peatlands can play an important role in the global carbon budget through permafrost carbon feedbacks and shifts in carbon assimilation. To better predict future dynamics in these ecosystems an increased understanding of their Holocene carbon and permafrost history is needed. In Tavvavuoma, northern Sweden, we have performed detailed analyses of vegetation succession and geochemical properties at six permafrost peatland sites. Peatland initiation took place around 10 000 to 9600 cal. a BP, soon after retreat of the Fennoscandian Ice Sheet, and the peatlands have remained permafrost‐free fens throughout most of the Holocene. At the four sites that showed a continuous accumulation record during the late Holocene radiocarbon dating of the shift from wet fen to dry bog vegetation, characteristic of the present permafrost peatland surface, suggests that permafrost developed at around 600–100 cal. a BP. At the other two sites peat accumulation was halted during the late Holocene, possibly due to abrasion, making it more difficult to imply the timing of permafrost aggradation. However also at these sites there are no indications of permafrost inception prior to the Little Ice Age. The mean long‐term Holocene carbon accumulation rate at all six sites was 12.3±2.4 gC m⁻² a⁻¹ (±SD), and the mean soil organic carbon storage was 114±27 kg m⁻².     

Response of peatland development and carbon cycling to climate change: a dynamic system modeling approach

Peatlands contain approximately 25% of the total soil organic carbon, despite covering only 3% of earth’s land surface. The ecological, hydrological and biogeochemical functions of peatlands are tightly coupled to climate. Therefore, both direct human impacts and indirect effects of climate change can threaten the ecological function of peatlands through changes in hydrology. However, little is known about how peatland ecosystems, and specifically their biogeochemistry, carbon cycling, and development, may respond to climatic change. In this study, the Peat Accumulation Model was adapted to investigate the response of peatland development and carbon cycling to climatic change through simulating changes in precipitation and temperature at different stages of peatland development history. The warming and wetting were imposed on this system at 10,000 years since its initialization (mid-development stage) and at 20,000 years since its initialization (late-development stage). Here, it was revealed that peatlands can switch between carbon sinks and sources suddenly, but the extent to which the change takes place depends on the developmental stage of peatland ecosystems. The simulation results for the late-development stage showed that peatlands could function as carbon sources once warming and wetting was imposed but that peatland ecosystems during the mid-development stage can still function as carbon sinks under warming and wetting conditions. Moreover, peatland ecosystems have self-regulation capabilities so that they can go back to their normal ecological and biogeochemical functions under newly stabilized climates. Also, it is the change in temperature that results in the fundamental change in peatland development and carbon cycling. This study indicates that the response of peatland ecosystems to climate change is largely determined by their developmental stages.     

Black carbon and organic carbon emissions from wildfires in Mexico

In Mexico, approximately 7650 wildfires occur annually, affecting 263 115 hectares of land. In addition to their impact on land degradation, wildfires cause deforestation, damage to ecosystems and promote land use change; apart from being the source of emissions of toxic substances to the environment (i.e., hydrogen cyanide, black carbon and organic carbon). Black carbon is a short-lived greenhouse pollutant that also promotes snow and ice melting and decreased rainfall; it has an estimated global warming potential close to 5000.¹ We present an estimate of the black carbon and organic carbon emissions from wildfires in Mexico from 2000 to 2012 using selected emission factors from the literature and activity data from local agencies. The results show average emissions of 5955 Mg/yr for black carbon and 62 085 Mg/yr for organic carbon. Black carbon emissions are estimated to be 14 888 Gg CO₂ equivalent (CO₂ eq) per year on average. With proper management of wildfires, such emissions can be mitigated. Moreover, improved air quality, conservation of ecosystems, improvement of visibility and maintenance of land use are a subset of the related co-benefits. Mitigating forest organic carbon emissions, which are ten times higher than black carbon emissions, would also prevent the morbidity and mortality impacts of toxic organic compounds in the environment.     

Holocene peat and carbon accumulation rates in the southern taiga of western Siberia

Although recent studies have recognized peatlands as a sink for atmospheric CO₂, little is known about the role of Siberian peatlands in the global carbon cycle. We have estimated the Holocene peat and carbon accumulation rate in the peatlands of the southern taiga and subtaiga zones of western Siberia. We explain the accumulation rates by calculating the average peat accumulation rate and the long-term apparent rate of carbon accumulation (LORCA) and by using the model of Clymo (1984, Philosophical Transactions of the Royal Society of London Series B 303, 605-654). At three key areas in the southern taiga and subtaiga zones we studied eight sites, at which the dry bulk density, ash content, and carbon content were measured every 10 cm. Age was established by radiocarbon dating. The average peat accumulation rate at the eight sites varied from 0.35 ± 0.03 to 1.13 ± 0.02 mm yr⁻¹ and the LORCA values of bogs and fens varied from 19.0 ± 1.1 to 69.0 ± 4.4 g C m⁻² yr⁻¹. The accumulation rates had different trends especially during the early Holocene, caused by variations in vegetation succession resulting in differences in peat and carbon accumulation rates. The indirect effects of climate change through local hydrology appeared to be more important than direct influences of changes in precipitation and temperature. River valley fens were more drained during wetter periods as a result of deeper river incision, while bogs became wetter. From our dry bulk density results and our age-depth profiles we conclude that compaction is negligible and decay was not a relevant factor for undrained peatlands. These results contribute to our understanding of the influence of peatlands on the global carbon cycle and their potential impact on global change.     

Dissolved carbon in pore waters from the carbonate barrier reef of Tahiti (French Polynesia) and its basalt basement

This paper deals with dissolved inorganic carbon (DIC) and organic carbon (DOC) in pore waters from a 150 m deep hole drilled through the carbonate barrier reef of Tahiti and its underlying basalt basement. Alkalinity-pH measurements were used to calculate the DIC species concentration, and DOC was analysed according to the high temperature catalytic oxidation technique. Salinity was used as a conservative tracer to help identify water origin and mixing within the hole. Water mixing, calcium carbonate dissolution and mineralization of organic carbon combined to form three distinct groups of pore water. In the deeper basalt layers, pore water with alkalinity of 1.4 meq kg^–1 pH of 7.6 and p(CO₂) of 1.2 mAtm was undersaturated with respect to both aragonite and calcite. In the intermediate carbonate layer, pore water with alkalinity of more than 2.0 meq kg^–1, pH of 7.70 and p(CO₂) of 1.4 mAtm was supersaturated with respect to both aragonite and calcite. The transition zone between those two groups extended between 80 and 100 m depth. The shift from aragonite undersaturation to supersaturation was mainly attributed to the mixing of undersaturated pore waters from the basalt basement with supersaturated pore waters from the overlaying limestone. In the top of the reef, inputs from a brackish water lens further increased p(CO₂) up to 5.6 times the atmospheric P(CO₂).     

Dissolved carbon in pore waters from the carbonate barrier reef of Tahiti (French Polynesia) and its basalt basement

This paper deals with dissolved inorganic carbon (DIC) and organic carbon (DOC) in pore waters from a 150 m deep hole drilled through the carbonate barrier reef of Tahiti and its underlying basalt basement. Alkalinity-pH measurements were used to calculate the DIC species concentration, and DOC was analysed according to the high temperature catalytic oxidation technique. Salinity was used as a conservative tracer to help identify water origin and mixing within the hole. Water mixing, calcium carbonate dissolution and mineralization of organic carbon combined to form three distinct groups of pore water. In the deeper basalt layers, pore water with alkalinity of 1.4 meq kg^?1 pH of 7.6 and p(CO₂) of 1.2 mAtm was undersaturated with respect to both aragonite and calcite. In the intermediate carbonate layer, pore water with alkalinity of more than 2.0 meq kg^?1, pH of 7.70 and p(CO₂) of 1.4 mAtm was supersaturated with respect to both aragonite and calcite. The transition zone between those two groups extended between 80 and 100 m depth. The shift from aragonite undersaturation to supersaturation was mainly attributed to the mixing of undersaturated pore waters from the basalt basement with supersaturated pore waters from the overlaying limestone. In the top of the reef, inputs from a brackish water lens further increased p(CO₂) up to 5.6 times the atmospheric P(CO₂).