Organic carbon accumulation rates in the Holocene and glacial Arabian Sea: implications for O2-consumption in the deep-sea and atmospheric CO2 variations

Variations in the deep-sea carbon reservoir have been invoked to explain the observed atmospheric carbon dioxide (CO₂) changes during glacial-interglacial cycles. In order to distinguish between the quantity of organic matter remineralized in the deep-sea and that permanently removed into sediments, we compared the bulk- and organic carbon-accumulation rates in Holocene and glacial sediments deposited below the oxygen minimum layer with total- and organic carbon fluxes to the deep Arabian Sea from continuous sediment trap deployments. This comparison shows that the mass of organic carbon remineralized at the sediment water interface is mainly a function of the bulk sediment flux. The oxygen consumed by the organic carbon remineralization is of the order of the observed oxygen deficiency of the modern deep Arabian Sea water. We use the evidence from the northern Indian Ocean to speculate on the possible effect of abiogenic mineral flux on the removal of organic carbon from upper layers of the world ocean to the deep-sea. We assume that if the bulk accumulation rate (not primary productivity) influences the flux of organic carbon (that is fixed from the atmosphere by marine organisms), then mineral matter flux will exert a significant control over atmospheric CO₂ contents. Model calculations incorporating transient changes in global bulk flux, caused by natural or anthropogenic changes, show that significant proportions of the observed changes in atmospheric CO₂ contents can be explained by this mechanism.This paper was presented at Clima Locarno 90, the International Conference on Past and Present Climate Dynamics: Reconstruction of Rates of Change, held in Locarno, Switzerland, September 24 to 28, 1991, organized by the Swiss National Climate Program — ProClim, with support from the Swiss Academy of Sciences. Guest editor for these papers is Dr. K. Kelts Offprint requests to: F Sirocko     

Modeling responses of the meadow steppe dominated by Leymus chinensis to climate change

Grassland is one of the most widespread vegetation types worldwide and plays a significant role in regional climate and global carbon cycling. Understanding the sensitivity of Chinese grassland ecosystems to climate change and elevated atmospheric CO₂ and the effect of these changes on the grassland ecosystems is a key issue in global carbon cycling. China encompasses vast grassland areas of 354 million ha of 17 major grassland types, according to a national grassland survey. In this study, a process-based terrestrial model the CENTURY model was used to simulate potential changes in net primary productivity (NPP) and soil organic carbon (SOC) of the Leymus chinensis meadow steppe (LCMS) under different scenarios of climatic change and elevated atmospheric CO₂. The LCMS sensitivities, its potential responses to climate change, and the change in capacity of carbon stock and sequestration in the future are evaluated. The results showed that the LCMS NPP and SOC are sensitive to climatic change and elevated CO₂. In the next 100 years, with doubled CO₂ concentration, if temperature increases from 2.7-3.9˚C and precipitation increases by 10% NPP and SOC will increase by 7-21% and 5-6% respectively. However, if temperature increases by 7.5-7.8˚C and precipitation increases by only 10% NPP and SOC would decrease by 24% and 8% respectively. Therefore, changes in the NPP and SOC of the meadow steppe are attributed mainly to the amount of temperature and precipitation change and the atmospheric CO₂ concentration in the future.     

Ocean dynamics determine the response of oceanic CO2 uptake to climate change

The increase of atmospheric CO₂ concentrations due to anthropogenic activities is substantially damped by the ocean, whose CO₂ uptake is determined by the state of the ocean, which in turn is influenced by climate change. We investigate the mechanisms of the ocean’s carbon uptake within the feedback loop of atmospheric CO₂ concentration, climate change and atmosphere/ocean CO₂ flux. We evaluate two transient simulations from 1860 until 2100, performed with a version of the Max Planck Institute Earth System Model (MPI-ESM) with the carbon cycle included. In both experiments observed anthropogenic CO₂ emissions were prescribed until 2000, followed by the emissions according to the IPCC Scenario A2. In one simulation the radiative forcing of changing atmospheric CO₂ is taken into account (coupled), in the other it is suppressed (uncoupled). In both simulations, the oceanic carbon uptake increases from 1 GT C/year in 1960 to 4.5 GT C/year in 2070. Afterwards, this trend weakens in the coupled simulation, leading to a reduced uptake rate of 10% in 2100 compared to the uncoupled simulation. This includes a partial offset due to higher atmospheric CO₂ concentrations in the coupled simulation owing to reduced carbon uptake by the terrestrial biosphere. The difference of the oceanic carbon uptake between both simulations is primarily due to partial pressure difference and secondary to solubility changes. These contributions are widely offset by changes of gas transfer velocity due to sea ice melting and wind changes. The major differences appear in the Southern Ocean (?45%) and in the North Atlantic (?30%), related to reduced vertical mixing and North Atlantic meridional overturning circulation, respectively. In the polar areas, sea ice melting induces additional CO₂ uptake (+20%).     

Uptake and Storage of Anthropogenic CO2 in the Pacific Ocean Estimated Using Two Modeling Approaches

A basin-wide ocean general circulation model(OGCM) of the Pacific Ocean is employed to estimate the uptake and storage of anthropogenic CO 2 using two different simulation approaches.The simulation(named BIO) makes use of a carbon model with biological processes and full thermodynamic equations to calculate surface water partial pressure of CO 2,whereas the other simulation(named PTB) makes use of a perturbation approach to calculate surface water partial pressure of anthropogenic CO 2.The results from the two simulations agree well with the estimates based on observation data in most important aspects of the vertical distribution as well as the total inventory of anthropogenic carbon.The storage of anthropogenic carbon from BIO is closer to the observation-based estimate than that from PTB.The Revelle factor in 1994 obtained in BIO is generally larger than that obtained in PTB in the whole Pacific,except for the subtropical South Pacific.This,to large extent,leads to the difference in the surface anthropogenic CO 2 concentration between the two runs.The relative difference in the annual uptake between the two runs is almost constant during the integration processes after 1850.This is probably not caused by dissolved inorganic carbon(DIC),but rather by a factor independent of time.In both runs,the rate of change in anthropogenic CO 2 fluxes with time is consistent with the rate of change in the growth rate of atmospheric partial pressure of CO 2.     

Diurnal variation of atmospheric CO<Subscript>2</Subscript> concentration and δ<Superscript>13</Superscript>C in an urban atmosphere during winter—role of the Nocturnal Boundary Layer

The paper presents the importance of the Nocturnal Boundary Layer in driving the diurnal variability of the atmospheric CO₂ mixing ratio and the carbon isotope ratio at ground level from an urban station in India. Our observations are the first of their kind from this region. The atmospheric CO₂ mixing ratio and the carbon isotopic ratio were measured for both the morning (05:30–07:30 IST) and afternoon time (16:00–18:00 IST) air samples at 5 m above ground level in Bangalore city, Karnataka State (12° 58′ N, 77° 38′ E, masl = 920 m) for a 10 day period during the winter of 2008. We observed a change of ~7% the in CO₂ mixing ratio between the morning and afternoon time air samples. A stable isotope analysis of CO₂ from morning samples showed a depletion in the carbon isotope ratio by ~2‰ compared to the afternoon samples. Along with the ground-based measurement of air samples, data of radiosonde measurements were also obtained from the Indian Meteorological Department to identify the vertical atmospheric structure at different time in a day. We proposed the presence or absence of the NBL as a controlling factor for the observed variability in the mixing ratio as well as its isotopic composition. Here we used the Keeling model approach to find out the carbon isotope ratio for the local sources. The local sources have further been characterized as anthropogenic and biological respiration (in %) using a two-component mixing model. We also used a vertical mixing model based on the concept of the mixing of isotopically depleted (carbon isotope) “polluted air” (PA) with isotopically enriched “free atmospheric air” (FA) above. Using this modeling approach, the contribution of FA at ground level is being estimated for both the morning and afternoon time air samples.     

The Potential Effects of Elevated Co2 and Climate Change on Tropical Forest Soils and Biogeochemical Cycling

Tropical forests are responsible for a large proportion of the global terrestrial C flux annually for natural ecosystems. Increased atmospheric CO₂ and changes in climate are likely to affect the distribution of C pools in the tropics and the rate of cycling through vegetation and soils. In this paper, I review the literature on the pools and fluxes of carbon in tropical forests, and the relationship of these to nutrient cycling and climate. Tropical moist and humid forests have the highest rates of annual net primary productivity and the greatest carbon flux from soil respiration globally. Tropical dry forests have lower rates of carbon circulation, but may have greater soil organic carbon storage, especially at depths below 1 meter. Data from tropical elevation gradients were used to examine the sensitivity of biogeochemical cycling to incremental changes in temperature and rainfall. These data show significant positive correlations of litterfall N concentrations with temperature and decomposition rates. Increased atmospheric CO₂ and changes in climate are expected to alter carbon and nutrient allocation patterns and storage in tropical forest. Modeling and experimental studies suggest that even a small increase in temperature and CO₂ concentrations results in more rapid decomposition rates, and a large initial CO₂ efflux from moist tropical soils. Soil P limitation or reductions in C:N and C:P ratios of litterfall could eventually limit the size of this flux. Increased frequency of fires in dry forest and hurricanes in moist and humid forests are expected to reduce the ecosystem carbon storage capacity over longer time periods.     

Declining Temporal Effectiveness of Carbon Sequestration: Implications for Compliance with the United National Framework Convention on Climate Change

Carbon sequestration is increasingly being promoted as a potential response to the risks of unrestrained emissions of CO₂, either in place of or as a complement to reductions in the use of fossil fuels. However, the potential role of carbon sequestration as an (at-least partial) substitute for reductions in fossil fuel use can be properly evaluated only in the context of a long-term acceptable limit (or range of limits) to the increase in atmospheric CO₂ concentration, taking into account the response of the entire carbon cycle to artificial sequestration. Under highly stringent emission-reduction scenarios for non-CO₂ greenhouse gases, 450 ppmv CO₂ is the equivalent, in terms of radiative forcing of climate,to a doubling of the pre-industrial concentration of CO₂. It is argued in this paper that compliance with the United Nations Framework Convention on Climate Change (henceforth, the UNFCCC) implies that atmospheric CO₂ concentration should be limited, or quickly returned to, a concentration somewhere below 450 ppmv. A quasi-one-dimensional coupled climate-carbon cycle model is used to assess the response of the carbon cycle to idealized carbon sequestration scenarios. The impact on atmospheric CO₂ concentration of sequestering a given amount of CO₂ that would otherwise be emitted to the atmosphere, either in deep geological formations or in the deep ocean, rapidly decreases over time. This occurs as a result of a reduction in the rate of absorption of atmospheric CO₂ by the natural carbon sinks (the terrestrial biosphere and oceans) in response to the slower buildup of atmospheric CO₂ resulting from carbon sequestration. For 100 years of continuous carbon sequestration, the sequestration fraction (defined as the reduction in atmospheric CO₂ divided by the cumulative sequestration) decreases to 14% 1000 years after the beginning of sequestration in geological formations with no leakage, and to 6% 1000 years after the beginning of sequestration in the deep oceans. The difference (8% of cumulative sequestration) is due to an eflux from the ocean to the atmosphere of some of the carbon injected into the deep ocean.The coupled climate-carbon cycle model is also used to assess the amount of sequestration needed to limit or return the atmospheric CO₂ concentration to 350–400 ppmv after phasing out all use of fossil fuels by no later than 2100. Under such circumstances, sequestration of 1–2 Gt C/yr by the latter part of this century could limit the peak CO₂ concentration to 420–460 ppmv, depending on how rapidly use of fossilfuels is terminated and the strength of positive climate-carbon cycle feedbacks. To draw down the atmospheric CO₂ concentration requires creating negative emissions through sequestration of CO₂ released as a byproduct of the production of gaseous fuels from biomass primary energy. Even if fossil fuel emissions fall to zero by 2100, it will be difficult to create a large enough negative emission using biomass energy to return atmospheric CO₂ to 350 ppmv within 100 years of its peak. However, building up soil carbon could help in returning CO₂ to 350 ppmv within 100 years of its peak. In any case, a 100-year period of climate corresponding to the equivalent of a doubled-CO₂ concentration would occur before temperatures decreased. Nevertheless, returning the atmospheric CO₂concentration to 350 ppmv would reduce longterm sea level rise due to thermal expansion and might be sufficient to prevent the irreversible total melting of the Greenland ice sheet, collapse of the West Antarctic ice sheet, and abrupt changes in ocean circulation that might otherwise occur given a prolonged doubled-CO₂ climate. Recovery of coral reef ecosystems, if not already driven to extinction, could begin.     

Role of the ocean in controlling atmospheric CO2 concentration in the course of global glaciations

Responses of ocean circulation and ocean carbon cycle in the course of a global glaciation from the present Earth conditions are investigated by using a coupled climate-biogeochemical model. We investigate steady states of the climate system under colder conditions induced by a reduction of solar constant from the present condition. A globally ice-covered solution is obtained under the solar constant of 92.2% of the present value. We found that because almost all of sea water reaches the frozen point, the ocean stratification is maintained not by temperature but by salinity just before the global glaciation (at the solar constant of 92.3%). It is demonstrated that the ocean circulation is driven not by the surface cooling but by the surface freshwater forcing associated with formation and melting of sea ice. As a result, the deep ocean is ventilated exclusively by deep water formation in southern high latitudes where sea ice production takes place much more massively than northern high latitudes. We also found that atmospheric CO₂ concentration decreases through the ocean carbon cycle. This reduction is explained primarily by an increase of solubility of CO₂ due to a decrease of sea surface temperature, whereas the export production weakens by 30% just before the global glaciation. In order to investigate the conditions for the atmospheric CO₂ reduction to cause global glaciations, we also conduct a series of simulations in which the total amount of carbon in the atmosphere?Cocean system is reduced from the present condition. Under the present solar constant, the results show that the global glaciation takes place when the total carbon decreases to be 70% of the present-day value. Just before the glaciation, weathering rate becomes very small (almost 10% of the present value) and the organic carbon burial declines due to weakened biological productivity. Therefore, outgoing carbon flux from the atmosphere?Cocean system significantly decreases. This suggests the atmosphere?Cocean system has strong negative feedback loops against decline of the total carbon content. The results obtained here imply that some processes outside the atmosphere?Cocean feedback loops may be required to cause global glaciations.     

The increasing CO2 concentration in the atmosphere and its implication on agricultural productivity

The increasing concentration of CO₂ in the atmosphere should result in a general increase in the net primary productivity of most cultivated species and forest species, assuming no counterproductive climatic changes occur. The photosynthetic rate of C₃ plants is most responsive to increasing concentration of CO₂ in the ambient air. C₄ plants demonstrate a stomatal closure that causes reduced transpiration. In the case of both types of plants, the water use efficiency (photosynthesis/transpiration) is likely to be improved.It has been suggested that photosynthetic production may be limited today more by shortages of water and nutrients than by shortages of carbon dioxide. The author speculates that the inadvertant CO₂-fertilization now occurring could, in itself, cause a moderate release from these constraints.Physiological responses to an increased atmospheric CO₂ concentration are easily demonstrated in controlled environment studies. Because of the difficulty in maintaining artifically enriched air near the crop against the forces of turbulent transfer, studies in the open field have been inconclusive. The observation of decreased photosynthetic rate in a perennial crop during that part of the growing season when CO₂ concentration is naturally low suggests a technique by which it may be possible to infer what will happen in the real world of agricultural fields if a CO₂-rich environment, such as is predicted in the coming decades, materializes. Inferences from the very limited set of data available support the view that net photosynthetic production will be increased.Published as Paper No. 6123, Journal Series, Nebraska Agricultural Experiment Station. The work reported was conducted under Regional Research Project 11–33 and Nebraska Agricultural Experiment Station Project 1149.George Holmes Professor of Agricultural Meteorology, Center for Agricultural Meteorology and Climatology, Institute of Agriculture and Natural Sources, University of Nebraska-Lincoln, Lincoln, NE 68583, U.S.A.     

A Case Study of CO<Subscript>2</Subscript>, CO and Particles Content Evolution in the Suburban Atmospheric Boundary Layer Using a 2-μm Doppler DIAL,a 1-μm Backscatter Lidar and an Array of In-situ Sensors

A network of remote and in-situ sensors was deployed in a Paris suburb in order to evaluate the mesoscale evolution of the daily cycle of CO₂ and related tracers in the atmospheric boundary layer (ABL) and its relation to ABL dynamics and nearby natural and anthropogenic sources and sinks. A 2-μm heterodyne Doppler differential absorption lidar, which combines measurements of, (1) structure of the atmosphere, (2) radial velocity, and (3) CO₂ differential absorption was a particularly unique element of the observational array. We analyse the differences in the diurnal cycle of CO, CO₂, lidar reflectivity (a proxy for aerosol content) and H₂O using the lidar, airborne measurements in the free troposphere and ground-based measurements made at two sites located few kilometres apart. We demonstrate that vertical mixing dominates the early morning drawdown of CO and aerosol content trapped in the former nocturnal layer but not the H₂O and CO₂ mixing ratio variations. Surface fluxes, vertical mixing and advection all contribute to the ABL CO₂ mixing ratio decrease during the morning transition, with the relative importance depending on the rate and timing of ABL rise. We also show evidence that when the ABL is stable, small-scale (0.1-km vertical and 1-km horizontal) gradients of CO₂ and CO are large. The results illustrate the complexity of inferring surface fluxes of CO₂ from atmospheric budgets in the stable boundary layer.     

Climate response to the physiological impact of carbon dioxide on plants in the Met Office Unified Model HadCM3

The concentration of carbon dioxide in the atmosphere acts to control the stomatal conductance of plants. There is observational and modelling evidence that an increase in the atmospheric concentration of CO₂ would suppress the evapotranspiration (ET) rate over land. This process is known as CO₂ physiological forcing and has been shown to induce changes in surface temperature and continental runoff. We analyse two transient climate simulations for the twenty-first century to isolate the climate response to the CO₂ physiological forcing. The land surface warming associated with the decreased ET rate is accompanied by an increase in the atmospheric lapse rate, an increase in specific humidity, but a decrease in relative humidity and stratiform cloud over land. We find that the water vapour feedback more than compensates for the decrease in latent heat flux over land as far as the budget of atmospheric water vapour is concerned. There is evidence that surface snow, water vapour and cloudiness respond to the CO₂ physiological forcing and all contribute to further warm the climate system. The climate response to the CO₂ physiological forcing has a quite different signature to that from the CO₂ radiative forcing, especially in terms of the changes in the temperature vertical profile and surface energy budget over land.     

太平洋海气CO2通量对气候事件的响应

应用一个嵌套了海洋生物地球化学循环的太平洋环流碳循环模式,分析了1960～2000年太平洋不同海区海气碳通量随时间的变化。模拟结果显示,赤道太平洋为大气CO₂的排放区,南、北太平洋(南、北纬15°至模式计算区域南、北边界)为吸收区。3个海区海气碳通量随时间均存在显著的波动,其中赤道太平洋海气碳通量年际波动最显著。3个海区海气碳通量年际波动对气候事件的响应并不一致,在El Niño年赤道太平洋冷舌的强度和总溶解无机碳(DIC)的浓度以及输出生产力均会受到上升流减弱的影响而降低,La Niña年这些海气碳通量控制要素的分布情况则正好相反,但在南北太平洋副热带以及高纬度海区,El Niño和La Niña对这些要素带来的影响却并不一定相反,对输出生产力的影响甚至是一致的。以海表温度(SST)为例考察海气碳通量与物理场之间的关系表明,在赤道太平洋上升流对DIC的影响是控制海气碳通量变化的主要因素,而在其他海区,尤其是副热带海区,由于垂直运动的年际变化较小,且生物生产力水平较低,SST的波动对海气碳通量年际变化的影响更加重要。     

Siberian CO2 efflux in winter as a CO2 source and cause of seasonality in atmospheric CO2

Over three years, we found a consistent CO₂ efflux from forest tundra of the Russian North throughout the year, including a large (89 g C m^–2 yr^–1) efflux during winter. Our results provide one explanation for the observations that the highest atmospheric CO₂ concentration and greatest seasonal amplitude occur at high latitudes rather than over the mid-latitudes, where fossil fuel sources are large, and where high summer productivity offset by winter respiration should give large seasonal oscillations in atmospheric CO₂. Winter respiration probably contributed substantially to the boreal winter CO₂ efflux. Respiration is an exothermic process that produces enough heat to warm soils and promote further decomposition. We suggest that, as a result of this positive feedback, small changes in surface heat flux, associated with human activities in the North or with regional or global warming, could release large quantities of organic carbon that are presently stored in permafrost.     

Acidification of Lower St. Lawrence Estuary Bottom Waters

Accumulation of metabolic CO₂ can acidify marine waters above and beyond the ongoing acidification of the ocean by anthropogenic CO₂. The impact of respiration on carbonate chemistry and pH is most acute in hypoxic and anoxic basins, where metabolic CO₂ accumulates to high concentrations. The bottom waters of the Lower St. Lawrence Estuary (LSLE), where persistently severe hypoxia has developed over the last 80 years, is one such case. We have reconstructed the evolution of pH in the bottom waters from historical and recent data, and from first principles relating the stoichiometry of CO₂ produced to oxygen consumed during microbial degradation of organic matter. Based on the value of the atmospheric partial pressure of CO₂ that best reproduces the preformed dissolved inorganic carbon concentration in the bottom waters, we estimate the average ventilation age of the bottom waters to be 16?±?3 years. The pH of the bottom waters has decreased by 0.2 to 0.3 over the last 75 years, which is four to six times greater than can be attributed to the uptake of anthropogenic CO₂. The pH decrease is accompanied by a decline in the saturation state with respect to both calcite and aragonite. As of 2007, bottom waters in the LSLE are slightly supersaturated with respect to calcite (Ω_c?≈?1.06?±?0.04) but are strongly undersaturated with respect to aragonite (Ω_a?≈?0.67?±?0.03).

     

Spectra of CO<Subscript>2</Subscript> and Water Vapour in the Marine Atmospheric Surface Layer

Spectra of CO₂ and water vapour fluctuations from measurements made in the marine atmospheric surface layer have been analyzed. A normalization of spectra based on Monin–Obukhov similarity theory, originally developed for wind speed and temperature, has been successfully extended also to CO₂ and humidity spectra. The normalized CO₂ spectra were observed to have somewhat larger contributions from low frequencies compared to humidity spectra during unstable stratification. However, overall, the CO₂ and humidity spectra showed good agreement as did the cospectra of vertical velocity with water vapour and CO₂ respectively. During stable stratification the spectra and cospectra displayed a well-defined spectral gap separating the mesoscale and small-scale turbulent fluctuations. Two-dimensional turbulence was suggested as a possible source for the mesoscale fluctuations, which in combination with wave activity in the vertical wind is likely to explain the increase in the cospectral energy for the corresponding frequency range. Prior to the analysis the turbulence time series of the density measurements were converted to time series of mixing ratios relative to dry air. Some differences were observed when the spectra based on the original density measurements were compared to the spectra based on the mixing ratio time series. It is thus recommended to always convert the density time series to mixing ratio before performing spectral analysis.     

Effects of increased CO2 levels on monsoons

Increased atmospheric carbon dioxide concentration provided warmer atmospheric temperature and higher atmospheric water vapor content, but not necessarily more precipitation. A set of experiments performed with a state-of-the-art coupled general circulation model forced with increased atmospheric CO₂ concentration (2, 4 and 16 times the present-day mean value) were analyzed and compared with a control experiment to evaluate the effect of increased CO₂ levels on monsoons. Generally, the monsoon precipitation responses to CO₂ forcing are largest if extreme concentrations of carbon dioxide are used, but they are not necessarly proportional to the forcing applied. In fact, despite a common response in terms of an atmospheric water vapor increase to the atmospheric warming, two out of the six monsoons studied simulate less or equal summer mean precipitation in the 16×CO₂ experiment compared to the intermediate sensitivity experiments. The precipitation differences between CO₂ sensitivity experiments and CTRL have been investigated specifying the contribution of thermodynamic and purely dynamic processes. As a general rule, the differences depending on the atmospheric moisture content changes (thermodynamic component) are large and positive, and they tend to be damped by the dynamic component associated with the changes in the vertical velocity. However, differences are observed among monsoons in terms of the role played by other terms (like moisture advection and evaporation) in shaping the precipitation changes in warmer climates. The precipitation increase, even if weak, occurs despite a weakening of the mean circulation in the monsoon regions (??precipitation-wind paradox??). In particular, the tropical east-west Walker circulation is reduced, as found from velocity potential analysis. The meridional component of the monsoon circulation is changed as well, with larger (smaller) meridional (vertical) scales.     

Effects of high CO2 levels on surface temperature and atmospheric oxidation state of the early Earth

One-dimensional radiative-convective and photochemical models are used to examine the effects of enhanced CO₂ concentrations on the surface temperature of the early Earth and the composition of the prebiotic atmosphere. Carbon dioxide concentrations of the order of 100–1000 times the present level are required to compensate for an expected solar luminosity decrease of 25–30%, if CO₂ and H₂O were the only greenhouse gases present. The primitive stratosphere was cold and dry, with a maximum H₂O volume mixing ratio of 10^–6. The atmospheric oxidation state was controlled by the balance between volcanic emission of reduced gases, photo-stimulated oxidation of dissolved Fe⁺² in the oceans, escape of hydrogen to space, and rainout of H₂O₂ and H₂CO. At high CO₂ levels, production of hydrogen owing to rainout of H₂O₂ would have kept the H₂ mixing ratio above 2×10^–4 and the ground-level O₂ mixing ratio below 10^–11, even if no other sources of hydrogen were present. Increased solar UV fluxes could have led to small changes in the ground-level mixing ratios of both O₂ and H₂.     

Factors influencing anthropogenic carbon dioxide uptake in the North Atlantic in models of the ocean carbon cycle

The uptake and storage of anthropogenic carbon in the North Atlantic is investigated using different configurations of ocean general circulation/carbon cycle models. We investigate how different representations of the ocean physics in the models, which represent the range of models currently in use, affect the evolution of CO₂ uptake in the North Atlantic. The buffer effect of the ocean carbon system would be expected to reduce ocean CO₂ uptake as the ocean absorbs increasing amounts of CO₂. We find that the strength of the buffer effect is very dependent on the model ocean state, as it affects both the magnitude and timing of the changes in uptake. The timescale over which uptake of CO₂ in the North Atlantic drops to below preindustrial levels is particularly sensitive to the ocean state which sets the degree of buffering; it is less sensitive to the choice of atmospheric CO₂ forcing scenario. Neglecting physical climate change effects, North Atlantic CO₂ uptake drops below preindustrial levels between 50 and 300 years after stabilisation of atmospheric CO₂ in different model configurations. Storage of anthropogenic carbon in the North Atlantic varies much less among the different model configurations, as differences in ocean transport of dissolved inorganic carbon and uptake of CO₂ compensate each other. This supports the idea that measured inventories of anthropogenic carbon in the real ocean cannot be used to constrain the surface uptake. Including physical climate change effects reduces anthropogenic CO₂ uptake and storage in the North Atlantic further, due to the combined effects of surface warming, increased freshwater input, and a slowdown of the meridional overturning circulation. The timescale over which North Atlantic CO₂ uptake drops to below preindustrial levels is reduced by about one-third, leading to an estimate of this timescale for the real world of about 50 years after the stabilisation of atmospheric CO₂. In the climate change experiment, a shallowing of the mixed layer depths in the North Atlantic results in a significant reduction in primary production, reducing the potential role for biology in drawing down anthropogenic CO₂.     

Multiple temporal scale variability during the twentieth century in global carbon dynamics simulated by a coupled climate–terrestrial carbon cycle model

A coupled climate–carbon cycle model composed of a process-based terrestrial carbon cycle model, Sim-CYCLE, and the CCSR/NIES/FRCGC atmospheric general circulation model was developed. We examined the multiple temporal scale functions of terrestrial ecosystem carbon dynamics induced by human activities and natural processes and evaluated their contribution to fluctuations in the global carbon budget during the twentieth century. Global annual net primary production (NPP) and heterotrophic respiration (HR) increased gradually by 6.7 and 4.7%, respectively, from the 1900s to the 1990s. The difference between NPP and HR was the net carbon uptake by natural ecosystems, which was 0.6 Pg C year^?1 in the 1980s, whereas the carbon emission induced by human land-use changes was 0.5 Pg C year^?1, largely offsetting the natural terrestrial carbon sequestration. Our results indicate that monthly to interannual variation in atmospheric CO₂ growth rate anomalies show 2- and 6-month time lags behind anomalies in temperature and the NiNO₃ index, respectively. The simulated anomaly amplitude in monthly net carbon flux from terrestrial ecosystems to the atmosphere was much larger than in the prescribed air-to-sea carbon flux. Fluctuations in the global atmospheric CO₂ time series were dominated by the activity of terrestrial vegetation. These results suggest that terrestrial ecosystems have acted as a net neutral reservoir for atmospheric CO₂ concentrations during the twentieth century on an interdecadal timescale, but as the dominant driver for atmospheric CO₂ fluctuations on a monthly to interannual timescale.