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1.
Variations of the atmospheric CO2 level and the global mean surface temperature during the last 150 Ma are reconstructed by using a carbon cycle model with high-resolution input data. In this model, the organic carbon budget and the CO2 degassing from the mantle, both of which would characterize the carbon cycle during the Cretaceous, are considered, and the silicate weathering process is formulated consistently with an abrupt increase in the marine strontium isotope record for the last 40 Ma. The second-order variations of the atmospheric CO2 level and the global mean surface temperature in addition to the first-order cooling trend are obtained by using high-resolution data of carbon isotopic composition of marine limestone, seafloor spreading rate, and production rate of oceanic plateau basalt. The results obtained from this model are in good agreement with the previous estimates of palaeo-CO2 level and palaeoclimate inferred from geological, biogeochemical, and palaeontological models and records. The system analyses of the carbon cycle model to understand the cause of the climate change show that the dominant controlling factors for the first-order cooling trend of climate change during the last 150 Ma are tectonic forcing such as decrease in volcanic activity and the formation and uplift of the Himalayas and the Tibetan Plateau, and, to a lesser extent, biological forcing such as the increase in the soil biological activity. The mid-Cretaceous was very warm because of the high CO2 level (4–5 PAL) maintained by the enhanced CO2 degassing rate due to the increased mantle plume activities and seafloor spreading rates at that time, although the enhanced organic carbon burial would have a tendency to decrease the CO2 level effectively at that period. The variation of organic carbon burial rate may have been responsible for the second-order climate change during the last 150 Ma.  相似文献   

2.
The importance of ocean temperature to global biogeochemistry   总被引：1，自引：0，他引：1  
Variations in the mean temperature of the ocean, on time scales from millennial to millions of years, in the past and projected for the future, are large enough to impact the geochemistry of the carbon, oxygen, and methane geochemical systems. In each system, the time scale of the temperature perturbation is key. On time frames of 1-100 ky, atmospheric CO2 is controlled by the ocean. CO2 temperature-dependent solubility and greenhouse forcing combine to create an amplifying feedback with ocean temperature; the CaCO3 cycle increases this effect somewhat on time scales longer than ∼5-10 ky. The CO2/T feedback can be seen in the climate record from Vostok, and a model including the temperature feedback predicts that 10% of the fossil fuel CO2 will reside in the atmosphere for longer than 100 ky. Timing is important for oxygen, as well; the atmosphere controls the ocean on short time scales, but ocean anoxia controls atmospheric pO2 on million-year time scales and longer. Warming the ocean to Cretaceous temperatures might eventually increase pO2 by approximately 25%, in the absence of other perturbations. The response of methane clathrate to climate change in the coming century will probably be small, but on longer time scales of 1-10 ky, there may be a positive feedback with ocean temperature, amplifying the long-term climate impact of anthropogenic CO2 release.  相似文献   

3.
河流作为连接陆地和海洋碳库之间的通道，是全球内陆水体碳排放最主要的载体，在全球碳循环中发挥着至关重要的作用。全球河流水-气界面二氧化碳（CO2）脱气显著的时间异质性特征研究有助于深入理解其碳循环过程与机制，也为准确评估碳通量以及完善碳循环模型提供了科学支撑。本文系统梳理了国内外的相关研究成果，总结了目前河流CO2脱气通量在昼夜、季节以及多年尺度上的动态变化及其影响因素，指出其昼夜变化与季节变化存在一定的周期性，并对不同空间尺度上CO2脱气通量的时间差异进行讨论。同时分析当前研究中的不足，认为缺乏河流二氧化碳分压（pCO2）与CO2脱气系数（k）高分辨率且长期连续的直接测量，限制了河流CO2脱气通量时间尺度变化的周期性及相互之间关系的厘定，使得气候变化与人类活动对河流CO2脱气时间动态的影响仍然难以量化与预测。最后，根据目前存在的问题，展望了未来的研究重点，为全球河流水-气界面碳循环过程与机制、模型研究提供新的思路与方向，以及可以更准确地评估和预测未来河流碳排放的变化趋势。  相似文献   

4.
In this paper, we use carbon isotopes in the dissolved load of rivers from the Lesser Antilles volcanic arc (Guadeloupe, Martinique and Dominica islands) to constrain the source of the carbon dioxide (CO2) involved in the neutralization reactions during water–rock interactions. The δ13C data span a large range of variations, from –19‰ to –5 · 2‰ for DIC (dissolved inorganic carbon) concentrations ranging from 11 μM to 2000 μM. Coupled with major element concentrations, carbon isotopic ratios are interpreted as reflecting a mixture of magmatic CO2 (enriched in heavy carbon (δ13C ≈ –3 · 5‰) and biogenic CO2 produced in soils (enriched in light carbon (δ13C < –17‰)). Carbon isotopes show that, at the regional scale, 23 to 40% of CO2 consumed by weathering reactions is of magmatic origin and is transferred to the river system through aquifers under various thermal regimes. These numbers remain first‐order estimates as the major uncertainty in using carbon isotopes as a source tracer is that carbon isotopes can be fractionated by a number of processes, including soil and river degassing. Chemical weathering is clearly, at least, partly controlled by the input of magmatic CO2, either under hydrothermal (hot) or surficial (cold) weathering regimes. This study shows that the contribution of magmatic CO2 to chemical weathering is an additional parameter that could explain the high weathering rates of volcanic rocks. The study also shows that a significant part of the carbon degassed from the Earth's interior is not released as CO2 to the atmosphere, but as DIC to the ocean because it interacts with the groundwater system. This study calls for a better understanding of the contributions of deep carbon to the hydrosphere and its influence on the development of the Critical Zone. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

5.
Projections of future climate change by climate system models depend on the sensitivities of models to specified greenhouse gases.To reveal and understand the different climate sensitivities of two versions of LASG/IAP climate system model FGOALS-g2 and FGOALS-s2,we investigate the global mean surface air temperature responses to idealized CO2 forcing by using the output of abruptly quadrupling CO2 experiments.The Gregory-style regression method is used to estimate the"radiative forcing"of quadrupled CO2 and equilibrium sensitivity.The model response is separated into a fast-response stage associated with the CO2 forcing during the first 20 years,and a slow-response stage post the first 20 years.The results show that the radiative forcing of CO2 is overestimated due to the positive water-vapor feedback and underestimated due to the fast cloud processes.The rapid response of water vapor in FGOALS-s2 is responsible for the stronger radiative forcing of CO2.The climate sensitivity,defined as the equilibrium temperature change under doubled CO2 forcing,is about 3.7 K in FGOALS-g2 and4.5 K in FGOALS-s2.The larger sensitivity of FGOALS-s2 is due mainly to the weaker negative longwave clear-sky feedback and stronger positive shortwave clear-sky feedback at the fast-response stage,because of the more rapid response of water vapor increase and sea-ice decrease in FGOALS-s2 than in FGOALS-g2.At the slow-response stage,similar to the fast-response stage,net negative clear-sky feedback is weaker in FGOALS-s2.Nevertheless,the total negative feedback is larger in FGOALS-s2 due to a larger negative shortwave cloud feedback that involves a larger response of total cloud fraction and condensed water path increase.The uncertainties of estimated forcing and net feedback mainly come from the shortwave cloud processes.  相似文献   

6.
Estimates of greenhouse gas evasion from rivers have been refined over the past decades to constrain their role in global carbon cycle processes. However, despite 55% of the human population living in urban areas, urban rivers have had limited attention. We monitored carbon dynamics in an urbanized river (River Kelvin, 331 km2, UK) to explore the drivers of dissolved carbon lateral and vertical export. Over a 2-year sampling period, riverine methane (CH4) and carbon dioxide (CO2) concentrations were consistently oversaturated with respect to atmospheric equilibria, leading to continual degassing to the atmosphere. Carbon stable isotopic compositions (δ13C) indicated that terrestrially derived carbon comprised most of the riverine CH4 and dissolved CO2 (CO2*) load while dissolved inorganic carbon (DIC) from groundwater was the main form of riverine DIC. The dynamics of CH4, CO2*, and DIC in the river were primarily hydrology-controlled, that is, [CH4] and [CO2*] both increased with elevated discharge, total [DIC] decreased with elevated discharge while the proportion of biologically derived DIC increased with increasing discharge. The concentration of dissolved organic carbon (DOC) showed a weak relationship with river hydrology in summer and autumn and was likely influenced by the combined sewer overflows. Carbon emission to the atmosphere is estimated to be 3.10 ± 0.61 kg C·m−2·yr−1 normalized to water surface area, with more than 99% emitted as CO2. Annual carbon loss to the coastal estuary is approximately 4.69 ± 0.70 Gg C yr−1, with annual DIC export approximately double that of DOC. Per unit area, the River Kelvin was a smaller carbon source to the atmosphere than natural rivers/streams but shows elevated fluxes of DIC and DOC under comparable conditions. This research illustrates the role urban systems may have on riverine carbon dynamics and demonstrates the potential tight link between urbanization and riverine carbon export.  相似文献   

7.
To prevent the recurrence of a disastrous eruption of carbon dioxide (CO2) from Lake Nyos, a degassing plan has been set up for the lake. Since there are concerns that the degassing of the lake may reduce the stability of the density stratification, there is an urgent need for a simulation tool to predict the evolution of the lake stratification in different scenarios. This paper describes the development of a numerical model to predict the CO2 and dissolved solids concentrations, and the temperature structure as well as the stability of the water column of Lake Nyos. The model is tested with profiles of CO2 concentrations and temperature taken in the years 1986 to 1996. It reproduces well the general mixing patterns observed in the lake. However, the intensity of the mixing tends to be overestimated in the epilimnion and underestimated in the monimolimnion. The overestimation of the mixing depth in the epilimnion is caused either by the parameterization of the k-epsilon model, or by the uncertainty in the calculation of the surface heat fluxes. The simulated mixing depth is highly sensitive to the surface heat fluxes, and errors in the mixing depth propagate from one year to the following. A precise simulation of the mixolimnion deepening therefore requires high accuracy in the meteorological forcing and the parameterization of the heat fluxes. Neither the meteorological data nor the formulae for the calculation of the heat fluxes are available with the necessary precision. Consequently, it will be indispensable to consider different forcing scenarios in the safety analysis in order to obtain robust boundary conditions for safe degassing. The input of temperature and CO2 to the lake bottom can be adequately simulated for the years 1986 to 1996 with a constant sublacustrine source of 18 l s–1 with a CO2 concentration of 0.395 mol l–1 and a temperature of 26 °C. The results of this study indicate that the model needs to be calibrated with more detailed field data before using it for its final purpose: the prediction of the stability and the safety of Lake Nyos during the degassing process.Responsible Editor: Hans Burchard  相似文献   

8.
The Nyangqu River, the largest right bank tributary of the Yarlung Zangbo River in the Qinghai–Tibet Plateau, was representative of an alpine riverine carbon cycle experiencing climate change. In this study, dissolved inorganic carbon (DIC) spatial and seasonal variations, as well as their carbon isotopic compositions (δ13CDIC) in river water and groundwater were systematically investigated to provide constraints on DIC sources, recharge and cycling. Significant changes in the δ13CDIC values (from −2.9‰ to −23.4‰) of the water samples were considered to be the result of different contributions of two dominant DIC origins: soil CO2 dissolution and carbonate weathering. Three types of rock weathering (dissolution of carbonate minerals by H2CO3 and H2SO4, and silicate dissolution by H2CO3) were found to control the DIC input into the riverine system. In DIC cycling, groundwater played a significant role in delivering DIC to the surface water, and DIC supply from tributaries to the main stream increased from the dry season to the wet season. Notably, the depleted δ13CDIC ‘peak’ around the 88.9° longitude, especially in the September groundwater samples, indicated the presence of ‘special’ DIC, which was attributed to the oxidation of methane from the Jiangsa wetland located nearby. This wetland could provide large amounts of soil organic matter available for bacterial degradation, producing 13C-depleted methane. Our study provided insights regarding the role of wetlands in riverine carbon cycles and highlighted the contribution of groundwater to alpine riverine DIC cycles.  相似文献   

9.
Hot springs in the Marsyandi Valley, Nepal, vent CO2 sourced from metamorphic fluids that mix with shallow groundwaters before degassing near the Earth's surface. The δ13C of spring waters ranges up to + 13‰, while that of the coexisting free gas phase is close to ? 4‰. Empirical and thermodynamic modelling of this isotopic fractionation suggests > 97 ± 1% CO2 degassing. The calculated minimum total CO2 degassing in the Marsyandi catchment is 5.4 × 109 mol/yr from a Cl-based estimate of the spring water discharge to the Marsyandi River and the fraction of CO2 degassed. Extrapolated to the whole of the Himalayas, this implies a probable minimum metamorphic CO2 flux of 0.9 × 1012 mol/yr, or ～ 13% of solid Earth CO2 degassing. The calculated flux is a factor of three greater than the estimated CO2 drawdown by silicate weathering in the Himalayas. Himalayan metamorphic degassing contributes a significant fraction of the global solid Earth CO2 flux and implies that metamorphism may cause changes in long-term climate that oppose those resulting from the orogenic forcing of chemical weatherability.  相似文献   

10.
Utilising newly available instrumentation, the carbon balance in two small tropical catchments was measured during two discharge events at high temporal resolution. Catchments share similar climatic conditions, but differ in land use with one draining a pristine rainforest catchment, the other a fully cleared and cultivated catchment. The necessity of high resolution sampling in small catchments was illustrated in each catchment, where significant chemical changes occurred in the space of a few hours or less. Dissolved and particulate carbon transport dominated carbon export from the rainforest catchment during high flow, but was surpassed by degassing of CO2 less than 4 h after the discharge peak. In contrast, particulate organic carbon dominated export from the cleared catchment, in all flow conditions with CO2 evasion accounting for 5–23% of total carbon flux. Stable isotopes of dissolved inorganic carbon (DIC) in the ephemeral rainforest catchment decreased quickly from ~1.5 ‰ to ~ ?16 ‰ in 5 h from the flood beginning. A two‐point mixing model revealed that in the initial pulse, over 90% of the DIC was of rainwater origin, decreasing to below 30% in low flow. In the cultivated catchment, δ13CDIC values varied significantly less (?11.0 to ?12.2 ‰) but revealed a complex interaction between surface runoff and groundwater sources, with groundwater DIC becoming proportionally more important in high flow, due to activation of macropores downstream. This work adds to an increasing body of work that recognises the importance of rapid, short‐lived hydrological events in low‐order catchments to global carbon dynamics. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

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