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1.
Measuring fluxes of greenhouse gases (GHGs) is fundamental to estimating their impact on global warming. We examined diurnal variations of carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) vertical fluxes in a tidal marsh ecosystem. Measurements were recorded on neap and spring tide days in April and September 2010 in the Shanyutan wetland of the Min River estuary, southeast China. Here, we define a positive flux as directing into the atmosphere. CH4 fluxes on the diurnal scale were positive throughout, and CH4 emissions into the atmosphere on neap tide days were higher than on spring tide days. CH4 releases from the marsh ecosystem on neap tide days were higher in the daytime; however, on spring tide days, daily variations of CH4 emissions were more complex. The marsh ecosystem plays a twofold role in both releasing and assimilating CO2 and N2O gases on the diurnal scale. Average CO2 fluxes were positive on the daily scale both on neap and spring days and were greater on the neap tide days than on spring tide days. Diurnal variations of N2O fluxes fluctuated more. Over the diurnal period, soil temperature markedly controlled variations of CH4 emissions compared to other soil factors, such as salinity and redox potential. Tidal water height was a key factor influencing GHGs fluxes at the water–air interface. Compared with N2O, the diurnal course of CO2 and CH4 fluxes in the marsh ecosystem appeared to be directly controlled by marsh plants. These results have implications for sampling and scaling strategies for estimating GHGs fluxes in tidal marsh ecosystems.  相似文献   

2.
中国农田的温室气体排放   总被引：70，自引：2，他引：70  
中国是一个农业大国,拥有约1.33百万平方公里的农田。这些田地的种植、翻耕、施肥、灌溉等管理措施不仅长期改变着农田生态系统中的化学元素循环,而且给全球气候变化带来影响。农业生态系统对全球变化的影响主要是通过改变3种温室气体,即二氧化碳(CO2)、甲烷(CH4)和氧化亚氮(N2O)在土壤-大气界面的交换而实现的。为了分析多种因素(如气候、土壤质地、农作物品种及各种农田经营管理措施等)对农业土壤释放CO22222222  相似文献   

3.
Freshwater marshes could be a source of greenhouse gases emission because they contain large amounts of soil carbon and nitrogen. These emissions are strongly influenced by exogenous nitrogen. We investigate the effects of exogenous nitrogen on ecosystem respiration (CO2), CH4 and N2O emissions from freshwater marshes in situ in the Sanjiang Plain Northeast of China during the growing seasons of 2004 and 2005, using a field fertilizer experiment and the static opaque chamber/GC techniques. The results show that there were no significant differences in patterns of seasonal variations of CO2 and CH4 among the fertilizer and non-fertilizer treatments, but the seasonal patterns of N2O emission were significantly influenced by the exogenous nitrogen. Seasonal averages of the CO2 flux from non-fertilizer and fertilizer were 987.74 and 1,344.35 mg m −2 h −1, respectively, in 2004, and 898.59 and 2,154.17 mg m −2 h −1, respectively, in 2005. And the CH4 from the control and fertilizer treatments were 6.05 and 13.56 mg m −2 h −1 and 0.72 and 1.88 mg m −2 h −1, respectively, in 2004 and 2005. The difference of N2O flux between the fertilizer and non-fertilizer treatments is also significant either in 2004 and 2005. On the time scale of 20-, 100-, and 500-year periods, the integrated global warming potential (GWP) of CO2 + CH4 + N2O released during the two growing seasons for the treatment of fertilizer was 97, 94 and 89%, respectively, higher than that for the control, which suggested that the nitrogen fertilizer can enhance the GWP of the CH4 and N2O either in long time or short time scale.  相似文献   

4.
Fluxes of methane (CH4) and carbon dioxide (CO2) to the atmosphere at 52 sites within a salt marsh were measured by a dark static chamber technique from mid July to mid September. Mean CH4 fluxes ranged from 0.2 mg m?2 d?1 to 11.0 mg m?2 d?1, with an overall average of 1.6 mg m?2 d?1. Flux of CH4 was inversely correlated (r2=0.23, p = 0.001) with salinity of the upper porewater at the site, suggesting the dominant role of SO4 2? in inhibiting methanogenesis in salt-marsh sediments. The combination of salinity and water table position was able to explain only 29% of the variance in CH4 emission. Mean soil flux of CO2 ranged from 0.3 g m?2 d?1 to 3.7 g m?2 d?1, with an overall average of 2.5 g m?2 d?1; it was correlated with aboveground biomass (positive, r2=0.38, p = 0.001) and position of the water table (negative, r2 = 0.55, p = 0.001). The combination of biomass and water table position accounted for 63% of the variance in CO2 flux. There were high variations in gas flux within the six plant communities. The sequences were CH4: upland edge > panne > pool > middle marsh > low marsh > high marsh, and CO2: middle marsh > low marsh > upland edge > high marsh > panne > pool. Compared to other salt-marsh systems, this Bay of Fundy marsh emits small amounts of CH4 and CO2.  相似文献   

5.
In order to better understand the spatiotemporal variations and interrelationships of greenhouse gases (GHG), monthly surface fluxes and profile concentrations of GHG (CO2, N2O and CH4) in karst areas in the Guizhou Province, southwest China, were measured from June 2006 to May 2007. GHG fluxes showed high variability, with a range of 460.9?C1,281.2?mg?m?2?h?1 for CO2, ?25.4 to 81.5???g?m?2?h?1 for N2O and ?28.7 to ?274.9???g?m?2?h?1 for CH4, but no obvious seasonal change trends of the fluxes existed. Profile concentrations of CO2, N2O and CH4 varied between 0.5 and 31.5?mL?L?1, 0.273 and 0.734, and 0.1 and 3.5???L?L?1, respectively. In general, concentrations of CO2 and N2O increased with depth, while CH4 had an inverse trend. However, in October, November and January, the reversal of depth patterns of GHG concentrations took place below 15?cm, close to the soil?Crock interface. The spatiotemporal distribution of CO2 in soil profile was significantly positively correlated with that of N2O (p?<?0.05?C0.01) and negatively correlated with that of CH4 (p?<?0.01). The correlation analysis showed that soil temperature and moisture may be responsible for GHG dynamics in the soils, rather than the exchange of GHG between land and atmosphere.  相似文献   

6.
The freshwater marshes in northern China are heavily impacted by anthropogenic disturbances such as cultivation and fertilization and increased levels of nutrients (especially N and P) through atmospheric deposition and agricultural surface runoff. These disturbances have affected the emission of N2O from these systems. This laboratory study was conducted to determine the effects of increased inputs of inorganic N and P on N2O emission from marsh soil in response to different soil moisture conditions. The results showed that the emission of N2O increased with the enhancement of N inputs when the soil was submerged, but that the highest N treatment suppressed the emission of N2O when the soil was at 60% water holding capacity (WHC), which may have occurred due to an inadequate amount of available C. Furthermore, the results of this study indicated that a small amount of N fertilizer induced much more N2O evolution from freshwater wetland soil, while P fertilizer inputs appeared to stimulate the emission of N2O only during the first few days of the experiment. Additionally, soil that was treated with P appeared to absorb N2O when it was at 60% WHC after around 6 weeks of the incubation, which indicates that the input of P fertilizer might serve as a shift of source or N2O sink in wetland soils under non-flooded conditions. When compared to soil at 60% WHC, submerged soil had significantly higher N2O emissions, except when subjected to the medial N treatment. These findings indicate that the soil moisture condition had a significant effect on N2O emissions when the same amount of N or P was applied. Therefore, the effects of N and P fertilization in the northern temperate wetlands cannot be neglected from regional or national emissions of N2O.  相似文献   

7.
Nitrous oxide (N2O) is a potent greenhouse gas. Mitigating N2O emission is critical for combating global climate change and improving the ecological environment. Many studies have focused on factors affecting N2O emission from agricultural soils, but rarely on the relationship among these factors. In the present study, continuous measurement on N2O emission was conducted in a maize system in Griffith, Australia and the relationships between N2O emission, soil properties and weather conditions were examined. Principal component analysis and path analysis were used to analyze these data in correlation coefficient and the direct and indirect effects to N2O emission. Results indicated that (1) the major factors affecting N2O emission were WFPS, mineralized nitrogen (Mineral N), daily mean temperature (T mean) and CO2 concentration. The factors of direct influence N2O emission were following Mineral N, CO2, WFPS, and T mean. The indirect influence N2O emission was following T mean, WFPS, Mineral N, and CO2 concentration. (2) The standard multiple regression describing the relationship between N2O emission and its major factors were Y = ?37.162 + 0.5267 X 1 + 0.4331 X 2 + 0.3014 X 3 + 0.2392 X 4 (r = 0.924, p < 0.01, n = 151), where Y is N2O emission, X 1 is Mineral N, X 2 is CO2, X 3 is WFPS and X 4 is T mean. (3) N2O emission from agricultural soils can be monitored and mitigated through improved management practices such as irrigation, straw retention and fertilizer application.  相似文献   

8.
Gas adsorption isotherms of Akabira coals were established for pure carbon dioxide (CO2), methane (CH4), and nitrogen (N2). Experimental data fit well into the Langmuir model. The ratio of sorption capacity of CO2, CH4, and N2 is 8.5:3.5:1 at a lower pressure (1.2 MPa) regime and becomes 5.5:2:1 when gas pressure increases to 6.0 MPa. The difference in sorption capacity of these three gases is explained by differences in the density of the three gases with increasing pressure. A coal–methane system partially saturated with CH4 at 2.4 MPa adsorption pressure was experimentally studied. Desorption behavior of CH4 by injecting pure CO2 (at 3.0, 4.0, 5.0, and 6.0 MPa), and by injecting the CO2–N2 mixture and pure N2 (at 3.0 and 6.0 MPa) were evaluated. Results indicate that the preferential sorption property of coal for CO2 is significantly higher than that for CH4 or N2. CO2 injection can displace almost all of the CH4 adsorbed on coal. When modeling the CH4–CO2 binary and CH2–CO2–N2 ternary adsorption system by using the extended Langmuir (EL) equation, the EL model always over-predicted the sorbed CO2 value with a lower error, while under-predicting the sorbed CH4 with a higher error. A part of CO2 may dissolve into the solid organic structure of coal, besides its competitive adsorption with other gases. According to this explanation, the EL coefficients of CO2 in EL equation were revised. The revised EL model proved to be very accurate in predicting sorbed ratio of multi-component gases on coals.  相似文献   

9.
The global warming of Earth’s near-surface, air and oceans in recent decades is a direct consequence of anthropogenic emission of greenhouse gases into the atmosphere such as CO2, CH4, N2O and CFCs. The CO2 emissions contribute approximately 60% to this climate change. This study investigates experimentally the aqueous carbonation mechanisms of an alkaline paper mill waste containing about 55 wt% portlandite (Ca(OH)2) as a possible mineralogical CO2 sequestration process. The overall carbonation reaction includes the following steps: (1) Ca release from portlandite dissolution, (2) CO2 dissolution in water and (3) CaCO3 precipitation. This CO2 sequestration mechanism was supported by geochemical modelling of final solutions using PHREEQC software, and observations by scanning electron microscope and X-ray diffraction of final reaction products. According to the experimental protocol, the system proposed would favour the total capture of approx. 218 kg of CO2 into stable calcite/ton of paper waste, independently of initial CO2 pressure. The final product from the carbonation process is a calcite (ca. 100 wt%)-water dispersion. Indeed, the total captured CO2 mineralized as calcite could be stored in degraded soils or even used for diverse industrial applications. This result demonstrates the possibility of using the alkaline liquid–solid waste for CO2 mitigation and reduction of greenhouse effect gases into the atmosphere.  相似文献   

10.
This study investigates the occurrence of greenhouse gases (GHGs) and the role of groundwater as an indirect pathway of GHG emissions into surface waters in a gaining stretch of the Triffoy River agricultural catchment (Belgium). To this end, nitrous oxide (N2O), methane (CH4) and carbon dioxide (CO2) concentrations, the stable isotopes of nitrate, and major ions were monitored in river and groundwater over 8 months. Results indicated that groundwater was strongly oversaturated in N2O and CO2 with respect to atmospheric equilibrium (50.1 vs. 0.55 μg L?1 for N2O and 14,569 vs. 400 ppm for CO2), but only marginally for CH4 (0.45 vs. 0.056 μg L?1), suggesting that groundwater can be a source of these GHGs to the atmosphere. Nitrification seemed to be the main process for the accumulation of N2O in groundwater. Oxic conditions prevailing in the aquifer were not prone for the accumulation of CH4. In fact, the emissions of CH4 from the river were one to two orders of magnitude higher than the inputs from groundwater, meaning that CH4 emissions from the river were due to CH4 in-situ production in riverbed or riparian zone sediments. For CO2 and N2O, average emissions from groundwater were 1.5?×?105 kg CO2 ha?1 year?1 and 207 kg N2O ha?1 year?1, respectively. Groundwater is probably an important source of N2O and CO2 in gaining streams but when the measures are scaled at catchment scale, these fluxes are probably relatively modest. Nevertheless, their quantification would better constrain nitrogen and carbon budgets in natural systems.  相似文献   

11.
Soils act as sources and sinks for greenhouse gases (GHG) such as carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O). Since both storage and emission capacities may be large, precise quantifications are needed to obtain reliable global budgets that are necessary for land-use management (agriculture, forestry), global change and for climate research. This paper discusses exclusively the soil emission-related processes and their influencing parameters. It reviews soil emission studies involving the most important land-cover types and climate zones and introduces important measuring systems for soil emissions. It addresses current shortcomings and the obvious bias towards northern hemispheric data.When using a conservative average of 300 mg CO2e m−2 h−1 (based on our literature review), this leads to global annual net soil emissions of ≥350 Pg CO2e (CO2e = CO2 equivalents = total effect of all GHG normalized to CO2). This corresponds to roughly 21% of the global soil C and N pools. For comparison, 33.4 Pg CO2 are being emitted annually by fossil fuel combustion and the cement industry.  相似文献   

12.
Much uncertainty exists in spatial and temporal variations of nitrous oxide (N2O) emissions from coastal marshes in temperate regions. To investigate the spatial and temporal variations of N2O fluxes and determine the environmental factors influencing N2O fluxes across the coastal marsh dominated by Suaeda salsa in the Yellow River estuary, China, in situ measurements were conducted in high marsh (HM), middle marsh (MM), low marsh (LM), and mudflat (MF) in autumn and winter during 2011–2012. Results showed that mean N2O fluxes and cumulative N2O emission indicated intertidal zone of the examined marshes as N2O sources over all sampling seasons with range of 0.0051 to 0.0152 mg N2O m?2 h?1 and 7.58 to 22.02 mg N2O m?2, respectively. During all times of day and the seasons measured, N2O fluxes from the intertidal zone ranged from ?0.0004 to 0.0644 mg N2O m?2 h?1. The freeze/thaw cycles in sediments during early winter (frequent short-term cycle) and midwinter (long-term cycle) were one of main factors affecting the temporal variations of N2O emission. The spatial variations of N2O fluxes in autumn were mainly dependent on tidal fluctuation and plant composition. The ammonia-nitrogen (NH4 +–N) in sediments of MF significantly affected N2O emissions (p < 0.05), and the high concentrations of Fe in sediments might affect the spatial variation of N2O fluxes. This study highlighted the large spatial variation of N2O fluxes across the coastal marsh (coefficient of variation (CV) = 127.86 %) and the temporal variation of N2O fluxes during 2011–2012 (CV = 137.29 %). Presently, the exogenous C and N loadings of the Yellow River estuary are increasing due to human activities; thus, the potential effects of exogenous C and N loadings on N2O emissions during early winter should be paid more attention as the N2O inventory is assessed precisely.  相似文献   

13.
Nitrous oxide evolution may contribute to partial destruction of the ozone layer in the stratosphere. A two year study of the release of N2O from adjoining salt, brackish, and fresh marsh sediment indicates that the annual emission was 31, 48, and 55 mg N m?2 respectively. Emission from open water area was less than the corresponding emission from the marsh sediment. In vitro experiments indicate that the N2O emission was increased when the sediment was drained for extended periods of time. The addition of NO3? significantly increased the rate of N2O evolution, indicating that a large potential for denitrification exists in the anoxic sediment. Appreciable losses of N2O would only be expected when the marshes receive an extraneous source of nitrate such as sewage and/or wastewater.The contribution of the Gulf Coast wetlands to the atmospheric N2O balance is estimated to be 3.3 × 109 g N2O. The maximum average daily emission was equivalent to 1.5 g N2O-N ha?1, which is less than the measured emission from uncultivated soils (Mosieret al., 1981) but greater than the estimates from noncropped land (CAST, 1976).  相似文献   

14.
Methane and CO2 emissions from the two most active mud volcanoes in central Japan, Murono and Kamou (Tokamachi City, Niigata Basin), were measured in from both craters or vents (macro-seepage) and invisible exhalation from the soil (mini- and microseepage). Molecular and isotopic compositions of the released gases were also determined. Gas is thermogenic (δ13CCH4 from −32.9‰ to −36.2‰), likely associated with oil, and enrichments of 13C in CO2 (δ13CCO2 up to +28.3‰) and propane (δ13CC3H8 up to −8.6‰) suggest subsurface petroleum biodegradation. Gas source and post-genetic alteration processes did not change from 2004 to 2010. Methane flux ranged within the orders of magnitude of 101-104 g m−2 d−1 in macro-seeps, and up to 446 g m−2 d−1 from diffuse seepage. Positive CH4 fluxes from dry soil were widespread throughout the investigated areas. Total CH4 emission from Murono and Kamou were estimated to be at least 20 and 3.7 ton a−1, respectively, of which more than half was from invisible seepage surrounding the mud volcano vents. At the macro-seeps, CO2 fluxes were directly proportional to CH4 fluxes, and the volumetric ratios between CH4 flux and CO2 flux were similar to the compositional CH4/CO2 volume ratio. Macro-seep flux data, in addition to those of other 13 mud volcanoes, supported the hypothesis that molecular fractionation (increase of the “Bernard ratio” C1/(C2 + C3)) is inversely proportional to gas migration fluxes. The CH4 “emission factor” (total measured output divided by investigated seepage area) was similar to that derived in other mud volcanoes of the same size and activity. The updated global “emission-factor” data-set, now including 27 mud volcanoes from different countries, suggests that previous estimates of global CH4 emission from mud volcanoes may be significantly underestimated.  相似文献   

15.
CH4 and CO2 fluxes from a high-cold swamp meadow and an alpine meadow on the Qinghai-Tibetan Plateau, subject to different degrees of degradation, were measured over a 12-month period. Air temperature, soil temperature and moisture, and the depths of the water table and thawing-freezing layer were determined. For swamp meadows, the greater the degradation, the lesser the carbon efflux. CH4 emissions at the nondegraded swamp meadow site were 1.09–3.5 and 2.5–11.27 times greater, and CO2 emissions 1.08–1.69 and 1.41–4.43 times greater, respectively, than those from moderately and severely degraded sites. For alpine meadows, the greater the degradation, the greater the CH4 consumption and CO2 emissions. CH4 consumption at the severely degraded alpine meadow site was 6.6–21 and 1.1–5.25 times greater, and CO2 emissions 1.05–78.5 and 1.04–6.28 times greater, respectively, than those from the nondegraded and moderately degraded sites. The CH4 and CO2 fluxes at both sites were significantly correlated (R 2 > 0.59, P < 0.05) with air temperature, soil temperature, and topsoil (0–5 cm depth) moisture, indicating these to be the main environmental factors affecting such fluxes.  相似文献   

16.
Mud volcanoes are important pathways for CH4 emission from deep buried sediments; however, the importance of gas fluxes have hitherto been neglected in atmospheric source budget considerations. In this study, gas fluxes have been monitored to examine the stability of their chemical compositions and fluxes spatially, and stable C isotopic ratios of CH4 were determined, for several mud volcanoes on land in Taiwan. The major gas components are CH4 (>90%), “air” (i.e. N2 + O2 + Ar, 1–5%) and CO2 (1–5%) and these associated gas fluxes varied slightly at different mud volcanoes in southwestern Taiwan. The Hsiao-kun-shui (HKS) mud volcano emits the highest CH4 concentration (CH4 > 97%). On the other hand, the Chung-lun mud volcano (CL) shows CO2 up to 85%, and much lower CH4 content (<37%). High CH4 content (>90%) with low CO2 (<0.2%) are detected in the mud volcano gases collected in eastern Taiwan. It is suggestive that these gases are mostly of thermogenic origin based on C1 (methane)/C2 (ethane) + C3 (propane) and δ13CCH4 results, with the exception of mud volcanoes situated along the Gu-ting-keng (GTK) anticline axis showing unique biogenic characteristics. Only small CH4 concentration variations, <2%, were detected in four on-site short term field-monitoring experiments, at Yue-shi-jie A, B, Kun-shui-ping and Lo-shan A. Preliminary estimation of CH4 emission fluxes for mud volcanoes on land in Taiwan fall in a range between 980 and 2010 tons annually. If soil diffusion were taken into account, the total amount of mud volcano CH4 could contribute up to 10% of total natural CH4 emissions in Taiwan.  相似文献   

17.
太湖及其周围河流中N2O的空间分布与释放通量   总被引：2，自引：1，他引：1       下载免费PDF全文
本次研究选择中国东部一个生态和环境空间分异极大的浅水湖泊（太湖）以及周围河流,分别于2003年7月和9月两次采集湖水和河水样品,分析其中的N2O浓度,并利用扩散模型公式估算水-气界面N2O交换通量。结果显示N2O饱和度的空间变化从70％不饱和到2708％过饱和变化范围很大。N2O饱和度的空间分布,N2O与CH4、无机氮、TDS（总溶解固体物质）之间的相关性都表明：   太湖重度富营养区N2O的产生极大地受到人为N输入的影响。然而,初步的通量分析显示湖泊N2O的释放因子不超过0.63％,小于河流中的默认值,N2O产率也略低于水环境中的平均值,太湖以面积为权重的释放通量平均值并不高,在7月和9月分别为14.0μmol/m2·d和9.7μmol/m2·d。这些结果表明流域人为N输入对整个湖泊N2O的促进作用是有限的,预计未来湖泊N2O释放不会因为人为活动增加而出现大幅度增加的状况。流域内各生态景观N2O释放量的比较,也表明富营养湖泊总体上仍然是一个十分有限的大气N2O释放源。相反,太湖周围河流存在较大的N2O释放速率,在7月和9月估算的N2O释放通量分别为142.1μmol/m2·d和28.8μmol/m2·d。将这一释放速率推广到整个流域后,预计河网的N2O释放量将占到耕作土壤的10％～50％,显示了河流对区域N2O质量平衡具有较重要的影响。  相似文献   

18.
Atmospheric methane, a more effective heat-trapping gas than CO2 that may affect climate change, has its greatest man-made source in the US from municipal solid waste (MSW) landfills. Consequently, the wise management of landfills can reduce these greenhouse gas emissions to the atmosphere. Methane from modern MSW landfills built with composite covers is frequently vented directly to the atmosphere. Biofiltration of landfill gas could oxidize CH4 to CO2 and water. Methane oxidation in old landfills with conventional soil covers can be effective in reducing the amount of CH4 emitted. In this study, comparison of methane emissions from three different landfill covers was conducted. Methane emissions from old landfills constructed with conventional soil covers, modern MSW landfills constructed with composite covers, and modern MSW landfills constructed with composite covers plus biofilters were calculated using the calculated CH4 oxidation rates. The results showed that an average of only 14% of the generated CH4 was emitted from landfills with modern composite covers plus biofilters, and an average of 85% of the generated CH4 was emitted from landfills with conventional covers when 100% of the generated CH4 emissions to the atmosphere from landfills with modern composite covers was assumed. By comparing the CH4 emission rates from three different landfill types, the use of a properly sized biofilter should be an effective technique to reduce CH4 emissions from landfills across the USA and potentially in many other areas of the world.  相似文献   

19.
The chemical and isotopic composition of fumarolic gases emitted from Nisyros Volcano, Greece, and of a single gas sample from Vesuvio, Italy, was investigated in order to determine the origin of methane (CH4) within two subduction-related magmatic-hydrothermal environments.Apparent temperatures derived from carbon isotope partitioning between CH4 and CO2 of around 340°C for Nisyros and 470°C for Vesuvio correlate well with aquifer temperatures as measured directly and/or inferred from compositional data using the H2O-H2-CO2-CO-CH4 geothermometer. Thermodynamic modeling reveals chemical equilibrium between CH4, CO2 and H2O implying that carbon isotope partitioning between CO2 and CH4 in both systems is controlled by aquifer temperature.N2/3He and CH4/3He ratios of Nisyros fumarolic gases are unusually low for subduction zone gases and correspond to those of midoceanic ridge environments. Accordingly, CH4 may have been primarily generated through the reduction of CO2 by H2 in the absence of any organic matter following a Fischer-Tropsch-type reaction. However, primary occurrence of minor amounts of thermogenic CH4 and subsequent re-equilibration with co-existing CO2 cannot be ruled out entirely. CO2/3He ratios and δ13CCO2 values imply that the evolved CO2 either derives from a metasomatized mantle or is a mixture between two components, one outgassing from an unaltered mantle and the other released by thermal breakdown of marine carbonates. The latter may contain traces of organic matter possibly decomposing to CH4 during thermometamorphism.  相似文献   

20.
Characteristics of trace gases (O3, CO, CO2, CH4 and N2O) and aerosols (particle size of 2.5 micron) were studied over the Arabian Sea, equatorial Indian Ocean and southwest part of the Bay of Bengal during the monsoon transition period (October–November, 2004). Flow of pollutants is expected from south and southeast Asia during the monsoonal transition period due to the patterns of wind flow which are different from the monsoon period. This is the first detailed report on aerosols and trace gases during the sampled period as the earlier Bay of Bengal Experiment (BOBMEX), Arabian Sea Monsoon Experiment (ARMEX) and Indian Ocean Experiments (INDOEX) were during monsoon seasons. The significant observations during the transition period include: (i) low ozone concentration of the order of 5 ppbv around the equator, (ii) high concentrations of CO2, CH4 and N2O and (iii) variations in PM2.5 of 5–20μg/m3.  相似文献   

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