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1.
《Quaternary Science Reviews》2007,26(5-6):732-742
The radiocarbon reservoir age of high latitude North Atlantic Ocean surface water is essential for linking the continental and marine climate records, and is expected to vary according to changes in North Atlantic deep water (NADW) production. Measurements from this region also provide important input and/or tests of oceanic radiocarbon using 3-D global ocean circulation models. Here, we present a surface water radiocarbon reservoir age record of the high latitude western North Atlantic for the deglacial period via the use of fossil cold-water corals growing in waters that are rapidly exchanged with nearby surface waters. The reservoir age of high latitude North Atlantic surface waters was computed from the radiocarbon age difference between our radiocarbon calibration record (http://radiocarbon.LDEO.columbia.edu) and our marine radiocarbon data. 230Th/234U/238U dates provide the absolute coral ages. Our high latitude North Atlantic Ocean reservoir age data combined with recalculated reservoir ages based on published coexisting terrestrial and marine material and Vedde ash radiocarbon dates from central and eastern North Atlantic show modern values (380±140 year, n=14) during the Bolling and Allerod warm period and a 200 year increase in reservoir age (590±130 year, n=10) during the entire Younger Dryas (YD) cold episode. The reservoir age then decreased to 270±20 year (n=2) at the Preboreal/YD transition, although the dates are too sparse for us to be confident in this estimate. We are not able to resolve the timing of the transition to increased reservoir ages from the mid-Allerod to the YD due to the relatively small change and correspondingly large uncertainty in the estimates. The atmospheric Δ14C record derived from our atmospheric radiocarbon record displays a 40 per mil increase from 12,900 to 12,650 cal years BP, coincident with the shift to high reservoir ages in the early YD cold event. Intrusion of 14C depleted Antarctic Intermediate Water (AAIW) to the high latitude North Atlantic and reduction of NADW formation are possible causes for the coincident shift to high reservoir ages in the North Atlantic surface ocean and increased atmospheric Δ14C during the beginning of the YD event.  相似文献   

2.
It is generally accepted view that the ventilation of Southern Ocean during the last deglaciation was the key factor in atmospheric CO2 rise. Further, other sites were identified, like the western equatorial Pacific, the Sub-Antarctic Atlantic and the eastern equatorial Pacific. Now there are evidences that CO2 was also released from the eastern Arabian Sea. The Arabian Sea is unique in characteristic, being land locked from the North and affected by monsoon winds and seasonal reversing circulations. Furthermore, the CO2 outgassing noticed during deglaciation makes it an interesting region to understand if the outgassing occurred from the deeper waters and hence led to any rise in deepwater \([\rm{CO}_3^{2-}]\).  相似文献   

3.
The 1986 lethal eruption of Lake Nyos (Cameroon) was caused by a sudden inversion between deep, CO2-loaded bottom lake waters and denser, gas-free surface waters. A deep CO2 source has been found in fluid inclusions which occur predominantly in clinopyroxenes from lherzolitic mantle xenoliths, brought to the surface by the last erupted alkali basalts. P–T conditions of CO2 trapping correspond to a gas density equal (or higher) than that of liquid water. It is suggested that this dense CO2, found in many ultrabasic mantle xenoliths worldwide, has accumulated at km depth, below a column of descending lake water. It may remain in a stable state for a long period, as long as the temperature is above the density inversion temperature for pure H2O/CO2 systems. At an estimated depth of about 3 km, cooling by descending waters (to about 30 °C) induces a density inversion for the upper part of the CO2 reservoir. This causes a constant, regular upstream of low-density CO2 which, in its turn, feeds the shallower lake density inversion.  相似文献   

4.
Carbon Capture and Storage (CCS) is one of the effective means to deal with global warming, and saline aquifer storage is considered to be the most promising storage method. Junggar Basin, located in the northern part of Xinjiang and with a large distribution area of saline aquifer, is an effective carbon storage site. Based on well logging data and 2D seismic data, a 3D heterogeneous geological model of the Cretaceous Donggou Formation reservoir near D7 well was constructed, and dynamic simulations under two scenarios of single-well injection and multi-well injection were carried out to explore the storage potential and CO2 storage mechanism of deep saline aquifer with real geological conditions in this study. The results show that within 100 km2 of the saline aquifer of Donggou Formation in the vicinity of D7 well, the theoretical static CO2 storage is 71.967 × 106 tons (P50)①, and the maximum dynamic CO2 storage is 145.295 × 106 tons (Case2). The heterogeneity of saline aquifer has a great influence on the spatial distribution of CO2 in the reservoir. The multi-well injection scenario is conducive to the efficient utilization of reservoir space and safer for storage. Based on the results from theoretical static calculation and the dynamic simulation, the effective coefficient of CO2 storage in deep saline aquifer in the eastern part of Xinjiang is recommended to be 4.9%. This study can be applied to the engineering practice of CO2 sequestration in the deep saline aquifer in Xinjiang.  相似文献   

5.
Geochemical investigations were carried out to define the origin of the low- to moderate-temperature thermal waters feeding the Monfalcone springs in northern Italy. Chemical data indicate that waters approach the composition of seawater. Mixing processes with cold low-salinity waters are highlighted. The δ18O and δD values are in the range ?5.0 to ?6.4 ‰, and ?33 to ?40 ‰, respectively, suggesting the dilution of the saline reservoir by karst-type freshwaters. A surplus of Ca2+ and Sr2+ ions with respect to a conservative mixing is ascribed to diagenetic reactions of the thermal waters with Cretaceous carbonates at depth. The measured Sr isotopic composition (87Sr/86Sr ratio) ranges between 0.70803 and 0.70814; after correction for the surplus Sr, a 87Sr/86Sr ratio indicating Miocene paleo-seawater is obtained. The dissolved gases indicate long-lasting gas–water interactions with a deep-originated gas phase of crustal origin, dominated by CO2 and marked by a water TDIC isotopic composition in the range ?5.9 to?8.8 and helium signature with 0.08?<?R/Ra?<?0.27, which is a typical range for the crust. A possible scenario for the Monfalcone thermal reservoir consists of Miocene marine paleowaters which infiltrated through the karstic voids formed within the prevalently Cretaceous carbonates during the upper Eocene emersion of the platform, and which were entrapped by the progressive burial by terrigenous sediments.  相似文献   

6.
A geochemical survey, in shallow aquifers and soils, has been carried out to evaluate the feasibility of natural gas (CH4) storage in a deep saline aquifer at Rivara (MO), Northern Italy. This paper discusses the areal distribution of CO2 and CH4 fluxes and CO2, CH4, Rn, He, H2 concentrations both in soils and shallow aquifers above the proposed storage reservoir. The distribution of pathfinder elements such as 222Rn, He and H2 has been studied in order to identify potential faults and/or fractures related to preferential migration pathways and the possible interactions between the reservoir and surface. A geochemical and isotopic characterization of the ground waters circulating in the first 200 m has allowed to investigation of (i) the origin of the circulating fluids, (ii) the gas–water–rock interaction processes, (iii) the amount of dissolved gases and/or their saturation status. In the first 200 m, the presence of CH4-rich reducing waters are probably related to organic matter (peat) bearing strata which generate shallow-derived CH4, as elsewhere in the Po Plain. On the basis of isotopic analysis, no hints of thermogenic CH4 gas leakage from a deeper reservoir have been shown. The δ13C(CO2) both in ground waters and free gases suggests a prevalent shallow origin of CO2 (i.e. organic and/or soil-derived). The acquisition of pre-injection data is strategic for the natural gas storage development project and as a baseline for future monitoring during the gas injection/withdrawing period. Such a geochemical approach is considered as a methodological reference model for future CO2/CH4 storage projects.  相似文献   

7.
The use of radioactive isotopes plays a very important role in dating groundwater, providing an apparent age of the systems in the framework of the aquifers conceptual modelling making available important features about the water fluxes, such as recharge, horizontal flow rates and discharge. In this paper, special emphasis has been put on isotopic constraints in the use of δ13C and 14C content as a dating tool in some hot (76 °C) and cold (17 °C) CO2-rich mineral waters discharging in the Vilarelho da Raia–Pedras Salgadas region (N-Portugal). The radiocarbon content determined in these CO2-rich mineral waters (14C activity from 4.3 up to 9.9 pmc) is incompatible with the systematic presence of 3H (from 1.7 to 7.9 TU). The δ13C values of the studied CO2-rich mineral waters indicate that the total C in the recharge waters is being masked by larger quantities of CO2 (14C-free) introduced from deep-seated (upper mantle) sources. This paper demonstrates that a good knowledge of mineral water systems is essential to allow hydrologists to make sound conclusions on the use of C isotopic data in each particular situation.  相似文献   

8.
The structure of the glacial ocean was significantly different to that of the present day with intermediate to mid-depth waters being notably more δ13C enriched than deep waters. This contrast was especially pronounced in the South Atlantic suggesting the development of a sharp chemical divide, or ‘chemocline’, at around 2500 m water depth between upper and lower layers, with implications for deep-ocean carbon storage [Hodell et al., 2003. Pleistocene vertical carbon isotope and carbonate gradients in the South Atlantic sector of the Southern Ocean. Geochemistry, Geophysics, Geosystems, 4(1): doi: 1004 10.1029/2002GC000367.]. We evaluate existing benthic foraminiferal δ13C, Cd/Ca and derived carbon isotope air–sea exchange signature (δ13Cas) data sets for the Atlantic during the Last Glacial Maximum (LGM), and Marine Isotope Stages (MIS) 6 and 8 in order to examine the regional extent of the chemocline in the South Atlantic. Benthic δ13C data north of the approximate latitude of the LGM Subantarctic Front (LGM-SAF, 43°S) linearly decrease with water depth, indicative of mixing between upper ‘well’ and lower ‘poorly’ ventilated water masses, with little evidence of the sharp chemical divide. Conversely, benthic δ13C data south of the LGM-SAF below 2500 m water depth are uniformly around ?0.8‰. The apparent δ13C gradient across the LGM-SAF suggests enhanced mid-depth ventilation north of the SAF and reduced ventilation to the south. From this pattern we conclude that the regional chemocline in the South Atlantic constituted a dominantly meridional, rather than a vertical gradient, and was developed during at least the past three glacial periods. Benthic Cd/Ca data indicate that the gradient was not nutrient related, although further data from the South Atlantic are needed for a better assessment of this suggestion. The combined benthic δ13C and Cd/Ca data indicate the source of well-ventilated upper waters in the South Atlantic changed from Northern Component Water (NCW) during early glacial phases to Upper Southern Component Water (USCW) during mid-to-late glacial phases when the Southern Ocean may have become isolated. USCW maintained a positive δ13C and δ13Cas signature simulating a North Atlantic origin that has been implicated in previous studies. The data demonstrate that secular imprints on δ13C must be taken into consideration when assessing the implications of the vertical δ13C gradient. This data also supports a variable water column architecture and modes of water mass formation as primary means to draw down atmospheric CO2 and storage in the abyssal ocean by involving processes occurring on either side of the SAF in the glacial Southern Ocean.  相似文献   

9.
Pore water profiles of total-CO2, pH, PO3?4, NO?3 plus NO?2, SO2?4, S2?, Fe2+ and Mn2+ have been obtained in cores from pelagic sediments of the eastern equatorial Atlantic under waters of moderate to high productivity. These profiles reveal that oxidants are consumed in order of decreasing energy production per mole of organic carbon oxidized (O2 > manganese oxides ~ nitrate > iron oxides > sulfate). Total CO2 concentrations reflect organic regeneration and calcite dissolution. Phosphate profiles are consistent with organic regeneration and with the effects of release and uptake during inorganic reactions. Nitrate profiles reflect organic regeneration and nitrate reduction, while dissolved iron and manganese profiles suggest reduction of the solid oxide phases, upward fluxes of dissolved metals and subsequent entrapment in the sediment column. Sulfate values are constant and sulfide is absent, reflecting the absence of strongly anoxic conditions.  相似文献   

10.
Underground geological storage of CO2 in deep saline aquifers is considered for reducing greenhouse gases emissions into the atmosphere. However, some issues were raised with regard to the potential hazards to shallow groundwater resources from CO2 leakage, brine displacement and pressure build-up. An overview is provided of the current scientific knowledge pertaining to the potential impact on shallow groundwater resources of geological storage of CO2 in deep saline aquifers, identifying knowledge gaps for which original research opportunities are proposed. Two main impacts are defined and discussed therein: the near-field impact due to the upward vertical migration of free-phase CO2 to surficial aquifers, and the far-field impact caused by large-scale displacement of formation waters by the injected CO2. For the near-field, it is found that numerical studies predict possible mobilization of trace elements but concentrations are rarely above the maximum limit for potable water. For the far-field, numerical studies predict only minor impacts except for some specific geological conditions such as high caprock permeability. Despite important knowledge gaps, the possible environmental impacts of geological storage of CO2 in deep saline aquifers on shallow groundwater resources appears to be low, but much more work is required to evaluate site specific impacts.  相似文献   

11.
Review: Thermal water resources in carbonate rock aquifers   总被引：3，自引：1，他引：2  
The current knowledge on thermal water resources in carbonate rock aquifers is presented in this review, which also discusses geochemical processes that create reservoir porosity and different types of utilisations of these resources such as thermal baths, geothermal energy and carbon dioxide (CO2) sequestration. Carbonate aquifers probably constitute the most important thermal water resources outside of volcanic areas. Several processes contribute to the creation of porosity, summarised under the term hypogenic (or hypogene) speleogenesis, including retrograde calcite solubility, mixing corrosion induced by cross-formational flow, and dissolution by geogenic acids from deep sources. Thermal and mineral waters from karst aquifers supply spas all over the world such as the famous bath in Budapest, Hungary. Geothermal installations use these resources for electricity production, district heating or other purposes, with low CO2 emissions and land consumption, e.g. Germany’s largest geothermal power plant at Unterhaching near Munich. Regional fault and fracture zones are often the most productive zones, but are sometimes difficult to locate, resulting in a relatively high exploration uncertainty. Geothermal installations in deep carbonate rocks could also be used for CO2 sequestration (carbonate dissolution would partly neutralise this gas and increase reservoir porosity). The use of geothermal installations to this end should be further investigated.  相似文献   

12.
Niutuozhen geothermal field is located in the Jizhong graben, belonging to the northern part of Bohai Bay Basin in North China. Chemical and isotopic analyses were carried out on 14 samples of the geothermal fluids discharged from Neogene Minghuazhen (Nm), Guantao (Ng), and Jixianian Wumishan (Jxw) formations. The δ2H and δ18O in water, δ13C in CH4, δ13C in CO2, and 3He/4He ratio in the gases were analyzed in combination with chemical analyses on the fluids in the Niutuozhen geothermal field. The chemical and isotopic compositions indicate a meteoric origin of the thermal waters. The reservoir temperatures estimated by chemical geothermometry are in the range between 60 and 108 °C. The results show that the gases are made up mainly by N2 (18.20–97.42 vol%), CH4 (0.02–60.95 vol%), and CO2 (0.17–25.14 vol%), with relatively high He composition (up to 0.52 vol%). The chemical and isotopic compositions of the gas samples suggest the meteoric origin of N2, predominant crustal origins of CH4, CO2, and He. The mantle-derived He contributions are calculated to be from 5 to 8% based on a crust–mantle binary mixing model. The deep temperatures in the Jxw reservoir were evaluated based on gas isotope geothermometry to be in the range from 141 to 165 °C. The mantle-derived heat fraction in the surface heat flow is estimated to be in the range of 48–51% based on 3He/4He ratios.  相似文献   

13.
Three geothermal systems, Montevago, Castellammare-Alcamo and Sciacca, are located along the main seismogenetic structures in Western Sicily. Concentrations of dissolved species including the gases CO2, N2, He and the results of stable isotope measurements δ18O, δD and δ13CTDIC in water samples collected from six thermal springs and 28 cold discharges were used to characterise their feeder aquifers and to reveal the relationships between water chemistry and regional seismicity. The Sciacca thermal springs differ chemically and isotopically from those of Montevago and the Castellammare-Alcamo areas. The inferred deep end-members of the thermal waters of Montevago and Castellammare-Alcamo are almost similar, suggesting that both systems are fed by carbonate waters and selenite waters. A slight contribution (1–3%) of seawater, during groundwater ascent it is also present. The Sciacca thermal springs are fed by a deep reservoir comprising a mixture of 50% carbonate water and 50% seawater. During ascent towards the surface, these waters interact with NaCl-rich evaporite layers. By combination of published and present data significant temporal variations of temperature and some chemical parameters in the thermal waters of Western Sicily have been recorded. These variations were mostly between 1966 and 1969. Although the data are discontinuous it is still possible to reveal a direct link between physico–chemical changes in the Acqua Pia and Terme Selinuntine springs and the 1968 Belice Valley earthquake. Within the studied springs, two kinds of geochemical behaviour have been recognised. The chemistry of the Montevago thermal springs was permanently changed in response to changes in the groundwater system. Water temperature and dissolved SO4, Cl, Na, and TDS showed minimum values before the earthquake and maximum values after the event. Almost constant values substantially higher than before, were recorded after the seismic event. Conversely, the temporal variations observed in the waters of the Terme Selinuntine spring, from 1965 to 1991, exhibit a transient increase most probably caused by a temporary contribution of deep CO2-rich fluids caused by the strain release during the 1968 earthquake.  相似文献   

14.
Geochemical detection of carbon dioxide in dilute aquifers   总被引：1，自引：0，他引：1  

Background  

Carbon storage in deep saline reservoirs has the potential to lower the amount of CO2 emitted to the atmosphere and to mitigate global warming. Leakage back to the atmosphere through abandoned wells and along faults would reduce the efficiency of carbon storage, possibly leading to health and ecological hazards at the ground surface, and possibly impacting water quality of near-surface dilute aquifers. We use static equilibrium and reactive transport simulations to test the hypothesis that perturbations in water chemistry associated with a CO2 gas leak into dilute groundwater are important measures for the potential release of CO2 to the atmosphere. Simulation parameters are constrained by groundwater chemistry, flow, and lithology from the High Plains aquifer. The High Plains aquifer is used to represent a typical sedimentary aquifer overlying a deep CO2 storage reservoir. Specifically, we address the relationships between CO2 flux, groundwater flow, detection time and distance. The CO2 flux ranges from 103 to 2 × 106 t/yr (0.63 to 1250 t/m2/yr) to assess chemical perturbations resulting from relatively small leaks that may compromise long-term storage, water quality, and surface ecology, and larger leaks characteristic of short-term well failure.  相似文献   

15.
Geologic carbon sequestration is the capture of anthropogenic carbon dioxide (CO2) and its storage in deep geologic formations. The processes of CO2 seepage into surface water after migration through water-saturated sediments are reviewed. Natural CO2 and CH4 fluxes are pervasive in surface-water environments and are good analogues to potential leakage and seepage of CO2. Buoyancy-driven bubble rise in surface water reaches a maximum velocity of approximately 30 cm s−1. CO2 rise in saturated porous media tends to occur as channel flow rather than bubble flow. A comparison of ebullition versus dispersive gas transport for CO2 and CH4 shows that bubble flow will dominate over dispersion in surface water. Gaseous CO2 solubility in variable-salinity waters decreases as pressure decreases leading to greater likelihood of ebullition and bubble flow in surface water as CO2 migrates upward.  相似文献   

16.
The reservoir temperature and conceptual model of the Pasinler geothermal area, which is one of the most important geothermal areas in Eastern Anatolia, are determined by considering its hydrogeochemical and isotope properties. The geothermal waters have a temperature of 51 °C in the geothermal wells and are of Na–Cl–HCO3 type. The isotope contents of geothermal waters indicate that they are of meteoric origin and that they recharge on higher elevations than cold waters. The geothermal waters are of immature water class and their reservoir temperatures are calculated as 122–155 °C, and their cold water mixture rate is calculated as 32%. According to the δ13CVPDB values, the carbon in the geothermal waters originated from the dissolved carbon in the groundwaters and mantle-based CO2 gases. According to the δ34SCDT values, the sources of sulfur in the geothermal waters are volcanic sulfur, oil and coal, and limestones. The sources of the major ions (Na+, Ca2+, Mg2+, Cl?, and HCO3 ?) in the geothermal waters are ion exchange and plagioclase and silicate weathering. It is determined that the volcanic rocks in the area have effects on the water chemistry and elements like Zn, Rb, Sr, and Ba originated from the rhyolite, rhyolitic tuff, and basalts. The rare earth element (REE) content of the geothermal waters is low, and according to the normalized REE diagrams, the light REE are getting depleted and heavy REE are getting enriched. The positive Eu and negative Ce anomalies of waters indicate oxygen-rich environments.  相似文献   

17.
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).  相似文献   

18.
Tekkehamam geothermal field is located in the South of Menderes Graben (Aegean region) and is one of the most important geothermal sites of Western Anatolia. Umut geothermal field is a part of the Tekkehamam field. This study was conducted in order to determine the origin and hydrogeochemical properties of the geothermal waters. For this purpose, sampling was done in order to check the chemistry of the water, and 18O, 2H isotope analyses done at four wells, nine natural springs and three cold water sources. According to the results of the chemical analysis, the geothermal waters were determined to be of Na + K-SO4 type. Additionally, 14C and 3H analyses were done in selected well and spring waters for the purpose of age determination of groundwater; most of the waters were determined to be submodern. Geothermometer calculations show that the reservoir temperature for the Umut geothermal field ranges between 148 and 180 °C. Stable isotope results indicate that Umut geothermal waters are meteoric in origin. Mixing between shallow and deep waters is the dominant subsurface process that determines the physical and chemical character of the waters.  相似文献   

19.
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).  相似文献   

20.
Ground waters in North Hesse (Germany) are conspicuous by high amounts of dissolved inorganic carbon (DIC) at low pH. The DIC is received from the uptake of soil CO2 and CO2 of volcanic origin and the subsequent dissolution ofTriassic and Permian limestone and dolomites. The volcanic CO2 is related to Miocene basaltic magma which has liberated gaseous CO2 during thebreakthrough to Triassic and Permian sediments. The volcanic CO2 (-6 < 13CCO2 < -3, PDB) was trapped within pore spacesand intra- and intergranulares of Permian evaporites and Triassic sandstones and was stored within such reservoirs until recent times. The uptake of volcanic CO2 occurs as ground water migrates through such reservoirs. The 13 C/12 C-signatures of the DIC indicate mixture of soil-CO2and CO2 of volcanic origin for the dissolution of marine limestone and dolomites. The obtained two types for CO2 of volcanic origin with 13CCO 2-values of -10 ± 3 and +2 ± 2 can be explained by diffusion of CO2 through micropores, faults, and interfacesof solids. This mobilisation of CO2 is accompanied with a kinetic fractionation of -9. 13 C-depleted CO2 is liberated from the reservoir,whereas 13 CO2 is accumulated in the residue  相似文献   

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