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1.
The dissolved methane (CH4) plume rising from the crater of the blowout well 22/4b in the Central North Sea was mapped during stratified water column conditions. Geochemical surveys were conducted close to the seafloor at 80.3 m water depth, below the thermocline (61.1 m), and in the mixed surface layer (13.2 m) using membrane inlet mass spectrometry (MIMS) in combination with a towed CTD. Seawater was continuously transferred from the respective depth levels of the CTD to the MIMS by using an inline submersible pump. Close to the seafloor a well-defined CH4 plume extended from the bubble release site ∼460 m towards the southwest. Along this distance CH4 concentrations decreased from a maximum of 7872 nmol l−1 to less than 250 nmol l−1. Below the thermocline the well-defined CH4 plume shape encountered at the seafloor was distorted and filaments were observed that extended towards the west and southwest in relation to current direction. Where the core of the bubble plume intersected this depth layer, footprints of high CH4 concentrations of up to 17,900 nmol l−1 were observed. In the mixed surface layer the CH4 distribution with a maximum of up to 3654 nmol l−1 was confined to a small patch of ∼60 m in diameter. The determination of the water column CH4 inventories revealed that CH4 transfer across the thermocline was strongly impeded as only ∼3% of the total water column inventory was located in the mixed surface layer. Best estimate of the CH4 seabed release from the blowout was 1751 tons yr−1. The fate of the trapped CH4 (∼97%) that does not immediately reach the atmosphere remains speculative. In wintertime, when the water column becomes well mixed as well as during storm events newly released CH4 and the trapped CH4 pool can be transported rapidly to the sea surface and emitted into the atmosphere.  相似文献   

2.
First direct evidence for ongoing gas seepage activity on the abandoned well site 22/4b (Northern North Sea, 57°55′ N, 01°38′ E) and discovery of neighboring seepage activity is provided from observations since 2005. A manned submersible dive in 2006 discovered several extraordinary intense seepage sites within a 60 m wide and 20 m deep crater cut into the flat 96 m deep seafloor. Capture and (isotope) chemical analyses of the gas bubbles near the seafloor revealed in situ concentrations of methane between 88 and 90%Vol. with δ13C–CH4 values around −74‰ VPDB, indicating a biogenic origin. Bulk methane concentrations throughout the water column were assessed by 120 Niskin water samples showing up to 400.000 nM CH4 in the crater at depth. In contrast, concentrations above the thermocline were orders of magnitude lower, with a median value of 20 nM. A dye tracer injection into the gas seeps revealed upwelling bubble and water motion with gas plume rise velocities up to ∼1 ms−1 (determined near the seabed). However, the dissolved dye did not pass the thermocline, but returned down to the seabed. Measurements of direct bubble-mediated atmospheric flux revealed low values of 0.7 ± 0.3 kty−1, much less than current state-of-the-art bubble dissolution models would predict for such a strong and upwelling in situ gas bubble flux at shallow water depths (i.e. ∼100 m).Acoustic multibeam water column imaging data indicate a pronounced 200 m lateral intrusion at the thermocline together with high methane concentration at this layer. A partly downward-orientated bubble plume motion is also visible in the acoustic data with potential short-circuiting in accordance to the dye experiment. This observation could partly explain the observed trapping of most of the released gas below the well-established thermocline in the North Sea. Moreover, 3D analyses of the multibeam water column data reveal that the upwelling plume transforms into a spiral expanding vortex while rising through the water column. Such a spiral vortex motion has never been reported before for marine gas seepage and might represent an important process with strong implication on plume dynamics, dissolution behavior, gas escape to the atmosphere, and is considered very important for respective modeling approaches.  相似文献   

3.
We discuss nitrous oxide (N2O) and methane (CH4) distributions in 49 vertical profiles covering the upper ∼300 m of the water column along two ∼13,500 km transects between ∼50°N and ∼52°S during the Atlantic Meridional Transect (AMT) programme (AMT cruises 12 and 13). Vertical N2O profiles were amenable to analysis on the basis of common features coincident with Longhurst provinces. In contrast, CH4 showed no such pattern. The most striking feature of the latitudinal depth distributions was a well-defined “plume” of exceptionally high N2O concentrations coincident with very low levels of CH4, located between ∼23.5°N and ∼23.5°S; this feature reflects the upwelling of deep waters containing N2O derived from nitrification, as identified by an analysis of N2O, apparent oxygen utilization (AOU) and NO3−, and presumably depleted in CH4 by bacterial oxidation. Sea-to-air emissions fluxes for a region equivalent to ∼42% of the Atlantic Ocean surface area were in the range 0.40–0.68 Tg N2O yr−1 and 0.81–1.43 Tg CH4 yr−1. Based on contemporary estimates of the global ocean source strengths of atmospheric N2O and CH4, the Atlantic Ocean could account for ∼6–15% and 4–13%, respectively, of these source totals. Given that the Atlantic Ocean accounts for around 20% of the global ocean surface, on unit area basis it appears that the Atlantic may be a slightly weaker source of atmospheric N2O than other ocean regions but it could make a somewhat larger contribution to marine-derived atmospheric CH4 than previously thought.  相似文献   

4.
Data from piston cores collected from Carolina Rise and Blake Ridge, and from many DSDP/ODP sites indicate that extreme 13C-depletion of methane and ΣCO2 occurs within the uppermost methanogenic zone of continental rise sediments. We infer that 13C-depleted methane is generated near the top of the methanogenic zone when carbon of 13C-depleted ΣCO2, produced by microbially-mediated anaerobic methane oxidation, is recycled back to methane through CO2 reduction. Interstitial water and gas samples were collected in 27 piston cores, 16 of which penetrated through the sulfate reduction zone into methane-bearing sediments of the Carolina Rise and Blake Ridge. Isotopic measurements (δ13CCH4, δ13CCO2, δDCH4, and δDH2O) indicate that this methane is microbial in origin, produced by microbially-mediated CO2 reduction. Methane samples form two distinct isotopic pools. (1) Methane from a seafloor seep site shows a mean δ13CCH4 value of − 69 ± 2%., mirroring values found at ≥ 160 mbsf from a nearby DSDP site. (2) Twenty, areally-separated sites (sample depth, 10 to 25 mbsf) have δ13CCH4 values ranging from −85 to −103%., and δ13CCO2 as negative as −48%.. The very low δ13C values from the methane and CO2 pools highlight the importance of carbon cycling within continental rise sediments at and near the sulfate-methane boundary.  相似文献   

5.
Atmospheric trace gas measurements were conducted during SEEDS-II. Atmospheric dimethylsulfide (DMS) was continuously measured by GC-MS during the R/V Hakuho cruise. Further, ambient air was sampled into canisters (42 samples) and analyzed by GC-MS and GC-FID for various biogenic and anthropogenic volatile organic compounds (VOCs) after the cruise. CO, O3, SO2, and NOx were monitored continuously aboard the ship.A fertilization experiment was conducted in a high-nitrate, low-chlorophyll (HNLC) region (48°N, 165°E). The atmospheric concentrations inside a patch (fertilized area) were compared with those outside it (natural area); however, clear differences were not observed for biogenic trace gasses (DMS, CH3Cl, CH3I, isoprene, and alkenes) in the atmosphere. However, a high DMS concentration was observed over the northwestern Pacific Ocean. The fertilized area was also observed by R/V Kilo Moana, and DMS was measured by GC-FPD. A good agreement was observed between the results of the measurements made aboard the two independent ships by different measurement methods.The atmospheric SO2 concentration was compared with the atmospheric DMS concentration. The SO2 concentration was found to vary with the atmospheric DMS concentration. A diurnal variation of the atmospheric DMS concentration was observed around the fertilized region. The DMS content tends to increase during the night and decrease during the day. A box model calculation was conducted to explain the diurnal variation of the atmospheric DMS. Since there was no diurnal variation of the wind speed, a constant DMS flux from the ocean surface was assumed. Further, the atmospheric OH radical concentration was assumed to be dependent on sunlight. The box model can roughly reproduce the atmospheric DMS diurnal variation mainly caused by its removal reaction with OH radicals.  相似文献   

6.
基于Sentinel-3载荷OLCI和SRAL数据的内波同步探测研究   总被引：1，自引：1，他引：0  
The ocean and land color instrument(OLCI) and synthetic aperture radar altimeter(SRAL) installed aboard the Sentinel-3 satellite have been in orbit for operational uses. In this study, data collected from Sentinel-3 are used to investigate internal waves in the South China Sea. An internal wave is detected using an OLCI image with a resolution of 300 m, and an analysis was performed with a quasi-synchronous moderate-resolution imaging spectroradiometer(MODIS) image. The opposite characteristics of OLCI and MODIS images of the same internal wave are explained by the critical angle in brightness reversals. The unique observational geometry of the OLCI image and its influence on observations of internal waves are discussed. The distribution of σ0 and sea surface height anomalies(SSHAs) induced by internal waves are studied using SRAL records. The σ0 records of SRAL occasionally show less sensitivity to the modulation of internal waves, which may be attributed to the observational geometry, while SSHAs show obvious variations. The synchronous pairing of OLCI images and SRAL records are analyzed to extract the three-dimensional sea surface signatures induced by internal waves. The analysis demonstrates that the profile of SSHAs in the surface shows an opposite phase to the profiles of internal waves in the ocean. The opposite phase relationship, observed in the remote sensing view, is also confirmed with a laboratory experiment.  相似文献   

7.
Temporal variations in the surface concentrations of two greenhouse gases (carbon dioxide and methane) in the atmosphere over a large city are studied on the basis of the data obtained during the 2003–2005 observations at a Moscow station for environmental monitoring. This station is based on the TROICA mobile observatory and located at the meteorological station of the Faculty of Geography, Moscow State University, on Vorob’evy gory. The methods of isolating the background concentrations of greenhouse gases under urban conditions are proposed, and the excess concentrations of CO2 and CH4 over their background values are estimated for different seasons and times of day. The CO2 and CH4 concentrations are shown to have more pronounced diurnal cycles in summer than in winter. The main causes of temporal variations in the surface concentrations of CO2 and CH4 under urban conditions and the differences between the mean concentrations of these greenhouse gases in Moscow and other areas of Russia are analyzed. It is shown that variations in the surface concentrations of carbon dioxide and methane on different time scales are caused by different atmospheric processes (global circulation, mesoscale gravity waves, surface temperature inversions, etc.)  相似文献   

8.
We present evidence for strong hydrothermal activity in the eastern Manus Basin (depth: 1700–2100 m), the existence of large scale triple-layered buoyant plumes at depths of 1100 m (“shallow plume”), 1700 m (“deep plume”), and 1400 m (“middle plume” with less extent than the other two plumes) that were revealed from water column anomalies of CH4, Mn, Al and pH observed in November to December 1990. Judging from the horizontal distribution of these parameters, the deep plume seems to originate from two distinct hydrothermal sites (eastern and western sites) in the research area, the eastern site being visually ascertained with deep-tow observations at the same time. The CH4/Mn ratio (mol mol−1) of the deep plume (0.02–0.05) is the lowest yet observed in hydrothermal plumes. The order of magnitude difference of CH4/Mn ratios between the shallow plume and the deep plume suggests that different kinds of fluid-rock interaction occurred to make the hydrothermal end members for the deep and shallow plumes. The shallow plume, which had an areal extent of more than 50 km, may be an episodic “megaplume”, because it was not recognized in the previous CH4 profiles in 1986, and because it has a similar CH4/Mn ratio as the megaplume observed in the North Fiji Basin. We found that the eastern deep plume is characterized by enormously high aluminium concentrations (0.6– 1.5 μmol kg−1), pH anomalies (0.1) and high Al/Mn ratios (10–17). The endmember fluid for the eastern deep plume may have an unusually low pH value to dissolve this much aluminum during fluid-rock interaction, or this plume may originate from an eruption-influenced fluid.  相似文献   

9.
China Marine Surveillance Force was equipped with modern aerial equipments for marine lawexecute with the advantage of functioning agilely at a large scale of surveillance coverage, providing powerful all-round safeguard, which is of benefit to the harmonious and sustainable development of coastal economy. Onboard the planes, three kinds of remote sensing sensors have been installed, including a marine airborne multi-spectrum scanner (MAMS), an optical-electronic platform, and an airborne hyper-spectral system AISA+. The specifications of remote sensing platforms were introduced briefly first, then examples of water quality monitoring by airborne remote sensing were presented, including the monitoring in coastal suspended material, oil-spill and abnormal warm water, etc.  相似文献   

10.
《Marine Geology》2006,225(1-4):129-144
Four mud extrusions were investigated along the erosive subduction zone off Costa Rica. Active fluid seepage from these structures is indicated by chemosynthetic communities, authigenic carbonates and methane plumes in the water column. We estimate the methane output from the individual mud extrusions using two independent approaches. The first is based on the amount of CH4 that becomes anaerobically oxidized in the sediment beneath areas covered by chemosynthetic communities, which ranges from 104 to 105 mol yr− 1. The remaining portion of CH4, which is released into the ocean, has been estimated to be 102–104 mol yr− 1 per mud extrusion. The second approach estimates the amount of CH4 discharging into the water column based on measurements of the near-bottom methane distribution and current velocities. This approach yields estimates between 104–105 mol yr−1. The discrepancy of the amount of CH4 emitted into the bottom water derived from the two approaches hints to methane seepage that cannot be accounted for by faunal growth, e.g. focused fluid emission through channels in sediments and fractures in carbonates. Extrapolated over the 48 mud extrusions discovered off Costa Rica, we estimate a CH4 output of 20·106 mol yr− 1 from mud extrusions along this 350 km long section of the continental margin. These estimates of methane emissions at an erosional continental margin are considerably lower than those reported from mud extrusion at accretionary and passive margins. Almost half of the continental margins are described as non-accretionary. Assuming that the moderate emission of methane at the mud extrusions off Costa Rica are typical for this kind of setting, then global estimates of methane emissions from submarine mud extrusions, which are based on data of mud extrusions located at accretionary and passive continental margins, appear to be significantly too high.  相似文献   

11.
The climate model of the Institute of Atmospheric Physics of the Russian Academy of Sciences (IAP RAS CM) has been supplemented with a module of soil thermal physics and the methane cycle, which takes into account the response of methane emissions from wetland ecosystems to climate changes. Methane emissions are allowed only from unfrozen top layers of the soil, with an additional constraint in the depth of the simulated layer. All wetland ecosystems are assumed to be water-saturated. The molar amount of the methane oxidized in the atmosphere is added to the simulated atmospheric concentration of CO2. A control preindustrial experiment and a series of numerical experiments for the 17th–21st centuries were conducted with the model forced by greenhouse gases and tropospheric sulfate aerosols. It is shown that the IAP RAS CM generally reproduces preindustrial and current characteristics of both seasonal thawing/freezing of the soil and the methane cycle. During global warming in the 21st century, the permafrost area is reduced by four million square kilometers. By the end of the 21st century, methane emissions from wetland ecosystems amount to 130–140 Mt CH4/year for the preindustrial and current period increase to 170–200 MtCH4/year. In the aggressive anthropogenic forcing scenario A2, the atmospheric methane concentration grows steadily to ≈3900 ppb. In more moderate scenarios A1B and B1, the methane concentration increases until the mid-21st century, reaching ≈2100–2400 ppb, and then decreases. Methane oxidation in air results in a slight additional growth of the atmospheric concentration of carbon dioxide. Allowance for the interaction between processes in wetland ecosystems and the methane cycle in the IAP RAS CM leads to an additional atmospheric methane increase of 10–20% depending on the anthropogenic forcing scenario and the time. The causes of this additional increase are the temperature dependence of integral methane production and the longer duration of a warm period in the soil. However, the resulting enhancement of the instantaneous greenhouse radiative forcing of atmospheric methane and an increase in the mean surface air temperature are small (globally < 0.1 W/m2 and 0.05 K, respectively).  相似文献   

12.
Atmospheric and dissolved methane (CH4) and nitrous oxide (N2O) were measured in the unique coastal ecosystem of theBoddenwaters, including the western Oder estuary, (southern Baltic Sea) during five campaigns between 1994 and 1997. The CH4saturations, ranging from 105–15 500%, showed great spatial and temporal variability with maximum values in September and minimum values in December. The N2O saturations were in the range of 91–312% with a maximum in March. Enhanced concentrations of both gases were observed only in the western Oder estuary near the mouth of the Peene River. Thus, we conclude that the distributions of CH4and N2O in the investigatedBoddenwaters are, directly or indirectly, linked to the Peene River runoff and not to the Oder River. Our estimate of the annual CH4emissions from theBoddenwaters to the atmosphere indicates a significant contribution (c. 17%) to the overall CH4emissions from the Baltic Sea. In contrast, theBoddenwaters represent only a small source for atmospheric N2O.CH4production rates estimated from sediment slurry experiments revealed a significant spatial variability and indicated that methanogenic activity was related to acetate consumption in the surface sediment layer. Sedimentary CH4production might depend on different amounts of accumulation of organic material.  相似文献   

13.
Measurements of methane (CH4) so far have always shown supersaturation in the entire North Sea relative to the atmospheric partial pressure and the distribution of surface CH4 reveals a distinct increase towards the shore. Since North Sea sediments presumably are an insignificant source for CH4 the coastal contribution via rivers and tidal flats gains in importance.In this work, CH4 data from the River Weser, the back barrier tidal flats of Spiekeroog Island (NW Germany), and the German Bight are presented. Results from the River Weser are compared to other rivers draining into the German Bight. Measurements in the tidal flat area of Spiekeroog Island highlight this ecosystem as an additional contributor to the overall CH4 budget of the southern North Sea. A tidally driven CH4 pattern is observed for the water column with maximum values during low tide. Tidal flat sediments turn out to be the dominating source because pore waters discharged during low tide are highly enriched in CH4. In contrast, the freshwater contribution to the tidal flats by small coastal tributaries has almost no impact on water column CH4 concentrations. The CH4 level seems to be disturbed irregularly by wind forcing due to elevated degassing and prevention of advective flow when tidal flats remain covered by water.Based on our data, two model calculations were used to estimate the impact of tidal flats on the CH4 budget in the German Bight. Our results demonstrate that the back barrier tidal flats of the east Frisian Wadden Sea contribute CH4 in an order of magnitude between the Wash estuary and River Elbe and thus have to be considered in budget calculations.  相似文献   

14.
MultiBeam echosounder data were collected during a surface-ship survey of the 22/4b well site in the North Sea in September 2011 using a Teledyne-Reson 7125. Modern multibeam echosounders are instrumental in providing detection and accurate localization of weak to strong bubble plumes. Two survey profiles effectively insonified the bubble plumes rising from the main crater at the well site, providing snapshot data of bubble plume processes. Additionally, three profiles insonified bubble plumes rising from, in, and to the south of a secondary crater, 1.2 km southeast of the main crater. Data processing included a simple algorithm that muted mislocated echoes from incomplete sidelobe suppression. The data processing produced a Cartesian volume of echo intensity from the water column and seabed.Plume geometry was analyzed to investigate a number of important large-scale plume processes, including plume bubble detrainment due to currents and stratification, downwelling flows, sea surface interaction, plume heterogeneity, and other fluid transport processes. The data showed strong upwelling flows, with bubble vertical motions generally much faster than currents. One important finding was that megaplumes create intrusions above the general thermocline, in part because their extensive upwelling flow lifts the thermocline locally. As a result, the intrusion layer deposits dissolved gases in the upper wave-mixed layer of the water column where it is not isolated from the atmosphere, unlike dissolved gases in the lower water column.The analysis shows that high fidelity multibeam echosounder data can provide a wealth of remote sensing information on bubble plume characteristics and processes, with important applications, including blowout monitoring and response, better understanding of megaplumes such as used in lake destratification, and improved characterization of natural seep emission processes.  相似文献   

15.
The stable carbon isotopic ratios (δ13C) of methane (CH4) and carbon dioxide (CO2) of gas-rich fluid inclusions hosted in fracture-fill mineralization from the southern part of the Lower Saxony Basin, Germany have been measured online using a crushing device interfaced to an isotopic ratio mass spectrometer (IRMS). The data reveal that CH4 trapped in inclusions seems to be derived from different source rocks with different organic matter types. The δ13C values of CH4 in inclusions in quartz hosted by Carboniferous rocks range between −25 and −19‰, suggesting high-maturity coals as the source of methane. Methane in fluid inclusions in minerals hosted by Mesozoic strata has more negative carbon isotope ratios (−45 to −31‰) and appears to represent primary cracking products from type II kerogens, i.e., marine shales. There is a positive correlation between increasing homogenization temperatures of aqueous fluid inclusions and less negative δ13C(CH4) values of in co-genetic gas inclusions probably indicating different mtaturity of the potential source rocks at the time the fluids were released. The CO2 isotopic composition of CH4-CO2-bearing inclusions shows slight negative or even positive δ13C values indicating an inorganic source (e.g., water-rock interaction and dissolution of detrital, marine calcite) for CO2 in inclusions. We conclude that the δ13C isotopic ratios of CH4-CO2-bearing fluid inclusions can be used to trace migration pathways, sources of gases, and alteration processes. Furthermore, the δ13C values of methane can be used to estimate the maturity of the rocks from which it was sourced. Results presented here are further supported by organic geochemical analysis of surface bitumens which coexist with the gas inclusion-rich fracture-fill mineralization and confirm the isotopic interpretations with respect to fluid source, type and maturity.  相似文献   

16.
海洋中生源活性气体的来源与迁移转化   总被引：1，自引：1，他引：0  
杨桂朋  张洪海 《海洋学报》2018,40(10):14-21
海洋生源活性气体主要包括二甲基硫（DMS）、甲烷（CH4）、氧化亚氮（N2O）、一氧化碳（CO）、挥发性卤代烃（VHCs）和非甲烷烃（NMHCs）等。它们通过海-气交换进入大气，不仅在全球碳、氮和硫循环中发挥关键作用，而且会直接或间接地对环境和气候变化产生重要影响。海洋释放的活性气体一类属于温室效应气体（CH4、N2O、VHCs和CO等），另一类会在大气中发生化学反应，控制着大气氧化平衡和臭氧浓度（VHCs和NMHCs）。而DMS属于负温室效应气体，其在大气中被快速氧化形成硫酸盐气溶胶，进而对云的形成和辐射强迫产生重要影响。本文综述了国内外海洋生源活性气体的研究现状，着重介绍了DMS、CH4和N2O的来源、迁移转化、海-气通量及其影响机制，并指明了该领域存在的科学问题及今后的研究方向。  相似文献   

17.
The results of measuring the methane content in the entire atmospheric thickness over the St. Petersburg region are given for 1991–2007. It is shown that, within this period, the mean annual cycle of the total methane content is characterized by its maximum values in December–January and its minimum values in June–August when the annual-cycle amplitude amounts to ∼3.6%. In this case, the annual variations in the total methane content may differ significantly from the mean annual cycle obtained in some years. A statistically significant linear trend of the total CH4 content has not been revealed for 1991–2007. The obtained values of the linear-trend index have opposite signs in the winter and summer months (positive for January 0.6 ± 0.2%/year and February 0.4 ± 0.2%/year and negative for July 0.3 ± 0.2%/year and August 0.2 ± 0.1%/year). This fact suggests the tendency for an increase in the amplitude of the annual cycle of the total CH4 content. The results of a spectral analysis of a series of data on the total CH4 content show that, for 1991–2007, the following harmonics are pronounced with a confidence of 95%: 12 months (annual harmonic), 32 months (quasi-biennial oscillations), and 55 months (4.5 years), which are also pronounced in the series of meteorological parameters and total ozone content.  相似文献   

18.
Considerable attention has focussed on methane hydrates as a potential energy resource but much less on the potential environmental problems of exploiting these deposits. In fact, methane hydrate deposits represent a dynamic system formed as a result of the continuous migration of methane gas along fracture systems. Any exploitation of methane hydrates offshore will perforce take place in these unstable systems and could lead to the large-scale release of CH4 under unfavourable circumstances. However, most of this CH4 would be oxidized to CO2 within the water column under steady-state conditions. Only under exceptional circumstances would large-scale release of CH4 into the atmosphere take place. The impact of exploiting these deposits offshore on global climate may therefore be limited provided serious efforts are made to minimize environmental impacts. At present, prospects for the commercial exploitation of methane hydrates are in their infancy. Considerable ingenuity will be required to satisfy the requirements of safe operating conditions, mitigation of environmental hazards and commercial viability. The need to exercise caution before attempting to exploit these deposits is emphasized.  相似文献   

19.
Detailed measurements of bubble composition, dissolved gas concentrations, and plume dynamics were conducted during a 9-month period at a very intense, shallow (22-m water depth) marine hydrocarbon seep in the Santa Barbara Channel, California. Methane, carbon dioxide, and heavier hydrocarbons were lost from rising seep bubbles, while nitrogen and oxygen were gained. Within the rising seawater bubble plume, dissolved methane concentrations were more than 4 orders of magnitude greater than atmospheric equilibrium concentrations. Strong upwelling flows were observed and bubble-rise times were ~40 s, demonstrating the rapid exchange of gases within the bubble plume.  相似文献   

20.
The principal statistical regularities typical of the behaviors of the CH4, CO, and CO2 concentrations in the atmospheric surface layer over the continental Russian territory are revealed from the measurements performed in 1997–2004 along the Trans-Siberian Railroad from Moscow to Khabarovsk with a mobile laboratory. The data obtained under the conditions of the atmosphere free of anthropogenic pollutants are analyzed. For near-background conditions, the typical continental methane, carbon monoxide, and carbon dioxide concentrations and characteristic features of their large-scale spatial distributions and daily variations, including those caused by surface inversions, are determined. Variations in the concentrations of these trace gases over industrial regions are analyzed. Our results are compared to the data obtained at background stations of the world network of atmospheric monitoring and to the data of a numerical simulation.  相似文献   

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