Origin of natural sulphur-bearing immiscible inclusions and H2S in oolite gas reservoir, Eastern Sichuan

Based on results of microscopic observation and laser Raman analysis about fluid inclusions, multiple special forms of immiscible inclusions that contain sulphur, liquid hydrocarbon, bitumen, etc. were discovered in samples collected from the H₂S gas reservoir-containing carbonates in the Lower Triassic Feixianguan Formation in the Jinzhu-Luojia area, Kai County, Sichuan Province. Based on the lithology and burial history of the strata involved as well as measurement results of homogenization temperature of fluid inclusions, bitumen reflectivity, etc., it is concluded that the H₂S in the gas reservoir resulted from the thermal reaction between hydrocarbons in reservoir and CaSO₄ in the gypsum-bearing dolostone section at the high temperature (140°C–17°C) oil-cracked gas formation stage in Late Cretaceous. Thereafter, research on a great number of immiscible inclusions in the reservoir reveals that elemental sulphur resulted from oxidation of part of the earlier-formed H₂S and further reaction between sulphates, hydrocarbons and H₂S in geological fluids in H₂S-bearing gas reservoir at a temperature of 86°C–89°C and a pressure of 340×10⁵Pa and during the regional uplift stage as characterized by temperature decrease and pressure decrease in Tertiary. Meanwhile, gypsum, anhydrite and calcite formed at this stage would trap particles like elemental sulphur and result in a variety of special forms of immiscible inclusions, and these inclusions would contain information concerning the complexity of the fluids in the reservoir and the origin of H₂S and natural sulphur in the gas reservoir.     

CO2-Hydrocarbon fluids of the Jade hydrothermal field in the Okinawa trough: fluid inclusion evidence

The Okinawa trough is a spreading back-are basin featuring emitting hydrothermal solutions (black chimney type) and modem sulfide precipitation on the sea floor. The study of fluid inclusions in water-rock interaction products in the Jade hydrothermal field indicates that the deep hydrothermal system beneath the sea floor is fairly rich in gas and there are two independent and coexisting fluids-CO₂-hydrocarbon fluid and salt aqueous fluid. On the whole, the composition of CO₂-hydrocarbon fluid inclusions is similar to that of the fluid inclusions in natural gas fields. The dominant composition of the inclusions in aqueous fluid is H₂O with CO₂ and CH₄ being oversaturated. The salt aqueous fluid of the Jade hydrothermal system might be emitted through a black chimney, whereas CO₂-rich fluids discharge CO₂ bubbles and CO₂ hydrate through fissures. Hydrocarbons in gas phase or in fluid might be enclosed somewhere under the sea. Large storage of CO₂-CH₄-H₂S gas or fluid and reaction of this gas or fluid with salt water will lead to commercial sulfide deposits.     

Basical characteristics of fluid geologic process of interlayer oxidation zone sandstone-type uranium deposit

This paper reveals the physicochemical properties such as component, formulation, genesis, tem-perature, pH, Eh, salinity and pressure of all main alteration fluid of interlayer oxidation zone sand-stone-type uranium deposits after studying the geologic process and geochemistry of internal typical sandstone-type uranium deposits such as Shihongtan deposit in the Turpan-Hami basin, 512 deposit in the Yili basin, Dongsheng deposit in the Ordos basin. The composition of fluid can be divided into two parts based on the analysis of inclusion: one can be affirmed as atmospheric water with ordinary temperature epigenesist according to the character of hydrogen and oxygen isotope of inclusion, the other is natural gas containing gaseous hydrocarbon like CH₄, and CO₂ as well as a little H₂S, CO, H₂, N₂ and so on, it always contains a small quantity of hydrocarbon liquid in petroliferous basins. The fluid property of oxidation alteration zone is always oxidation alkaline, and neutrality or weak acid-weak alkaline and reducibility during the metallizing process, but at secondary reduction or deoxidization zone it becomes strong reduction alkaline. Oxygenic groundwater in the fluid is the activate and mig-ratory medium of uranium element, but the gaseous hydrocarbon like CH₄ as well as H₂, H₂S, CO from natural gas is the important sedimentary reducer of uranium mineral; the transformation of pH,Eh in fluid environment is the main reason for the formation of uranium metallization.     

Characteristics and accumulation mechanisms of the Dongfang 13-1 high temperature and overpressured gas field in the Yinggehai Basin,the South China Sea

The Dongfang 13-1 is located in the diapiric structure belt of the Yinggehai Basin. The formation pressure of its main gas reservoir in the Miocene Huangliu Formation is up to 54.6 MPa(pressure coefficient=1.91) and the temperature is as high as 143°C(geothermal gradient 4.36°C/100 m), indicating that it is a typical high-temperature and overpressured gas reservoir. The natural gas is interpreted to be coal-type gas derived from the Miocene mature source rocks containing type II2-III kerogens as evidenced by high dryness index of up to 0.98 and heavy carbon isotopes, i.e., the δ13C1 ranging from -30.76‰ to -37.52‰ and δ13C2 ranging from -25.02‰ to -25.62‰. The high temperature and overpressured Miocene petroleum system is related mainly to diapir in the Yinggehai Basin and contains more pore water in the overpressured reservoirs due to undercompaction process. The experimental and calculated results show that the solubility of natural gas in formation water is as high as 10.5 m3/m3 under the temperature and pressure conditions of the Sanya Formation, indicating that at least part of the gas may migrate in the form of water-soluble phase. Meanwhile, the abundant gas source in the Basin makes it possible for the rapid saturation of natural gas in formation water and exsolution of soluble gas. Therefore, the main elements controlling formation of the Dongfang 13-1 gas pool include that(1) the diapir activities and accompanying changes in temperature and pressure accelerate the water-soluble gas exsolution and release a lot of free gas;(2) submarine fan fine sandstone in the Huangliu Formation provides good gas-water segregation and accumulation space; and(3) the overlying overpressured mud rocks act as effective caps. The accumulation mechanism reveals that the high temperatural and high pressure structure belt near the diapir structures has a good potential for large and medium-sized gas field exploration.     

Organic and inorganic geochemistry of low temperature gas discharges at the Baia di Levante beach, Vulcano Island, Italy

Discharge from subaereal and submarine gas vents of the Baia di Levante beach gases from the Vulcano Island were sampled for major and trace gas components in May and November 1995.Chemical compositions and equilibrium calculations suggest three different groups of CO₂-rich gas emissions depending on their distance from the La Fossa crater: (1) gas vents close to the Faraglione area are characterised by high H₂S contents, high calculated equilibrium temperatures based on inorganic species and relatively high proportion of alkene compounds; (2) gas vents close to Vulcanello are characterised by low calculated equilibrium temperatures and low amounts of alkenes; and (3) Pontile sample has the highest equilibrium CO₂ pressure (up to 68 bars) which may account for the observed absence of benzene. The relative large variability of H₂S in the Baia di Levante beach gas discharge may be attributed to either different interactions between iron sulphides and weakly acid waters or catalytic effect of elemental sulphur on the de-hydrogenation of cyclo-hexane. Thermodynamic calculations suggest that the main inorganic species and CH₄ may have re-equilibrated at relatively shallow depth (10–200 m b.s.l. and 30–600 m b.s.l. for a lithostatic and hydrostatic pressure, respectively). The slow kinetics of reactions in the C_nH_2n/C_nH_2n+2 systems, with respect to that of CH₄–CO–CO₂, may explain the observed propene/propane ratios, which can only be reached at reaction temperatures of 300–350°C. This low speed of reactions can also explain the observed disequilibrium of C1–C4 alkanes.     

Mapping of H2S fluxes from the ground using copper passive samplers: An application study at the Zolforata di Pomezia degassing area (Alban Hills,Central Italy)

A new method for measuring H₂S mass flux from the ground, based on the digital analysis of the interference colours produced by the sulphidation of copper passive samplers (CPS), is proposed and discussed in this article. CPS sulphidation has a wide range of linear responses to H₂S doses and can be used together the accumulation chamber method to estimate gas fluxes from natural degassing areas. These are often characterized by the presence of vent centred degassing areas (VCDAs), which are recognizable from the absence or rarefaction of vegetation due to high acid gas concentrations in the soil pores and in the air at ground level. A reference emission curve, accounting for the advective and diffusive components of the flux, can be modelled and used to estimate the total H₂S mass released from each VCDA. The application of this method can be supported by remote sensing analysis that helps identify VCDAs in the field in perivolcanic H₂S degassing areas.As an illustrative application, H₂S gas fluxes from the ground were measured in spring 2007 at the Zolforata di Pomezia degassing area (ZPDA, Alban Hills, Central Italy) using an accumulation chamber internally equipped with CPS. H₂S peak fluxes were measured over the vents after remote sensing assisted identification of the VCDAs. Further measurements were carried out in two ponds and one artificial channel bordering the study area. The total atmospheric flux released at the ZPDA, estimated to be about 1207.6 kg day^? 1, was calculated as the summation of the fluxes from all the H₂S sources, the background flux being negligible.     

Rare gas constraints on hydrocarbon accumulation, crustal degassing and groundwater flow in the Pannonian Basin

The isotopic composition and abundances of He, Ne and Ar have been measured in a sequence of vertically stacked gas reservoirs at Hajduszoboszlo and Ebes, in the Pannonian Basin of Hungary. The gas reservoirs occur at depths ranging from 727 to 1331 m, are CH₄ dominated and occupy a total rock volume of approximately 1.5 km³. There are systematic variations in both major species abundances and rare gas isotopic composition with depth: CO₂ and N₂ both increase from 0.47 and 1.76% to 14.1 and 30.5%, respectively, and ⁴⁰Ar/³⁶Ar and ²¹Ne/²²Ne increase systematically from 340 and 0.02990 at 727 m to 1680 and 0.04290 at 1331 m. A mantle-derived He component between 2 and 5% is present in all samples, the remainder is crustal-radiogenic He. The Ar and Ne isotope variations arise from mixing between atmosphere-derived components in groundwater, and crustally produced radiogenic Ar and Ne. The atmosphere-derived ⁴⁰Ar and ²¹Ne decreases from 85 and 97% of the total ⁴⁰Ar and ²¹Ne at 727 m to 18 and 68% at 1331 m. The deepest samples are shown to have both atmosphere-derived and radiogenic components close to the air-saturated water and radiogenic production ratios. The shallowest samples show significant fractionation of He/Ar and Ne/Ar ratios in atmosphere-derived and radiogenic rare gas components, but little or no fractionation of He/Ne ratios. This suggests that diffusive fractionation of rare gases is relatively unimportant and that rare gas solubility partitioning between CH₄ and H₂O phases controls the observed rare gas elemental abundances.The total abundance of atmosphere-derived and radiogenic rare gas components in the Hajduszoboszlo gas field place limits on the minimum volume of groundwater that has interacted with the natural gas, and the amount of crust that has degassed and supplied radiogenic rare gases. The radiogenic mass balance cannot be accounted for by steady state production either within the basin sediments or the basement complex since basin formation. The results require that radiogenic rare gases are stored at their production ratios on a regional scale and transported to the near surface with minimal fractionation. The minimum volume of groundwater required to supply the atmosphere-derived rare gases would occupy a rock volume of some 1000 km³ (assuming an average basin porosity of 5%), a factor of 670 greater than the reservoir volume. Interactions between groundwater and the Hajduszoboszlo hydrocarbons has been on a greater scale than often envisaged in models of hydrocarbon formation and migration.     

Isotopic evidence of TSR origin for natural gas bearing high H<Subscript>2</Subscript>S contents within the Feixianguan Formation of the northeastern Sichuan Basin,southwestern China

The northeastern area of Sichuan Basin, southwestern China, is the area with the maximal reserve of natural gas containing higher hydrogen sulphide (H₂S) that has been found among the petroliferous basins of China, with the proven and controlled gas reserve of more than 200 billion cubic meters. These gas pools, with higher H₂S contents averaging 9%, some 17%, are mainly distributed on structural belts of Dukouhe, Tieshanpo, Luojiazhai, Puguang, etc., while the oolitic-shoal dolomite of the Triassic Feixianguan Fm. (T₁f) is the reservoir. Although many scholars regard the plentiful accumulation of H₂S within the deep carbonate reservoir as the result of Thermochemical Sulfate Reduction (TSR), however, the process of TSR as well as its residual geological and geochemical evidence is still not quite clear. Based on the carbon isotopic analysis of carbonate strata and secondary calcite, etc., together with the analysis of sulfur isotopes within H₂S, sulphur, gypsum, iron pyrites, etc., as well as other aspects including the natural gas composition, carbon isotopes of hydrocarbons reservoir petrology, etc., it has been proved that the above natural gas is a product of TSR. The H₂S, sulphur and calcite result from the participation of TSR reactions by hydrocarbon gas. During the process for hydrocarbons being consumed due to TSR, the carbons within the hydrocarbon gas participate in the reactions and finally are transferred into the secondary calcite, and become the carbon source of secondary calcite, consequently causing the carbon isotopes of the secondary calcite to be lower (−18.2‰). As for both the intermediate product of TSR, i.e. sulfur, and its final products, i.e. H₂S and iron pyrites, their sulfur elements are all sourced from the sulfate within the Feixianguan Fm. During the fractional processes of sulfur isotopes, the bond energy leads to the ³²S being released firstly, and the earlier it is released, the lower δ ³⁴S values for the generated sulphide (H₂S) or sulfur will be. However, for the anhydrite that participates in reactions, the higher the reaction degree, the more ³²S is released, while the less ³²S remains and the more δ ³⁴S is increased. The testing results have proved the process of the dynamic fractionation of sulfur isotopes.     

Coseismic changes in the chemical composition of volcanic gases from the Owakudani geothermal area on Hakone volcano,Japan

The chemical and isotopic compositions of volcanic gases at a borehole and a natural fumarole in the Owakudani geothermal area, Hakone volcano, Japan, have been repeatedly measured since 2001, when a seismic swarm occurred in the area. The CO₂/H₂O and CO₂/H₂S ratios were high in 2001. It increased in 2006 and again in 2008 when seismic swarms occurred beneath the geothermal area. The observed increases suggest the injection of CO₂- and SO₂-rich magmatic gas into the underlying hydrothermal reservoir, implying that the magmatic gas was episodically supplied to the hydrothermal system in 2006 and 2008. The earthquake swarms probably resulted from the injection of gas through the shallow crust accompanying the break of the sealing zone.     

An isotope study of the accumulation mechanisms of high-sulfur gas from the Sichuan Basin,southwestern China

The mechanism of hydrogen sulfide (H₂S) generation plays a key role in the exploration and development of marine high-sulfur natural gas, of which the major targets are the composition and isotope characteristics of sulfur-containing compounds. Hydrocarbon source rocks, reservoir rocks, natural gases and water-soluble gases from Sichuan Basin have been analyzed with an online method for the content of H₂S and isotopic composition of different sulfur-containing compounds. The results of comparative analysis show that the sulfur-containing compounds in the source rocks are mainly formed by bacterial sulfate reduction (BSR), and the sulfur compounds in natural gas, water and reservoir are mainly formed by thermal sulfate reduction (TSR). Moreover, it has been shown that the isotopically reversion for methane and ethane in high sulfur content gas is caused by TSR. The sulfur isotopic composition of H₂S in natural gas is inherited from the gypsum or brine of the same or adjacent layer, indicating that the generation and accumulation of H₂S have the characteristics of either a self-generated source or a near-source.     

Measuring Concentrations of Dissolved Methane and Ethane and the 13C of Methane in Shale and Till

Baseline characterization of concentrations and isotopic values of dissolved natural gases is needed to identify contamination caused by the leakage of fugitive gases from oil and gas activities. Methods to collect and analyze baseline concentration‐depth profiles of dissolved CH₄ and C₂H₆ and δ¹³C‐CH₄ in shales and Quaternary clayey tills were assessed at two sites in the Williston Basin, Canada. Core and cuttings samples were stored in Isojars^® in a low O₂ headspace prior to analysis. Measurements and multiphase diffusion modeling show that the gas concentrations in core samples yield well‐defined and reproducible depth profiles after 31‐d equilibration. No measurable oxidative loss or production during core sample storage was observed. Concentrations from cuttings and mud gas logging (including IsoTubes^®) were much lower than from cores, but correlated well. Simulations suggest the lower concentrations from cuttings can be attributed to drilling time, and therefore their use to define gas concentration profiles may have inherent limitations. Calculations based on mud gas logging show the method can provide estimates of core concentrations if operational parameters for the mud gas capture cylinder are quantified. The δ¹³C‐CH₄ measured from mud gas, IsoTubes^®, cuttings, and core samples are consistent, exhibiting slight variations that should not alter the implications of the results in identifying the sources of the gases. This study shows core and mud gas techniques and, to a lesser extent, cuttings, can generate high‐resolution depth profiles of dissolved hydrocarbon gas concentrations and their isotopes.     

Numerical evaluation of the shear stimulation effect in naturally fractured formations

In shale gas fracking, the stimulated natural fracture system is often critical to the gas production. In this paper, we present the results of state-of-the-art modeling of a detailed parametric evolution of the shear stimulation effect in discrete fracture network (DFN) formations. Two-dimensional computational modeling studies have been used in an attempt towards understanding how naturally fractured reservoirs response in hydraulic fracturing. Simulations were conducted as a function of: (1) the in-situ stress ratio; (2) internal friction angle of DFN; (3) DFN orientation with the stress field; and (4) operational variables such as injection rate. A sensitivity study reveals a number of interesting observations resulting from these parameters on the shear stimulation in natural fracture system. This work strongly links the production technology, geomechanical evaluation and aids in the understanding and optimization of hydraulic fracturing simulations in naturally fractured reservoirs.     

Viscosity of a Teide phonolite in the welding interval

The viscosity of a natural phonolitic composition with variable amounts of H₂O has been experimentally determined. The starting materials were crystal-free phonolitic glasses from Montaña Blanca, situated within the Las Cañadas caldera of Teide. Dry phonolitic melt viscosities were determined using concentric cylinder viscometry in the low viscosity range. The glassy quench products of these runs were then hydrated by high pressure synthesis in a piston–cylinder apparatus to generate a suite of samples with water contents ranging from 0.02 to 3.75 wt%. Samples thus hydrated were quenched rapidly and prepared (cut and polished) for the determination of water contents by infrared spectroscopy before and after experimental viscometry. The viscosities of the melts (dry and hydrated) were determined at 1 bar using a micropenetration technique. Samples were stable under the measurement conditions up to 3.75 wt% H₂O. Homogeneity of water content was confirmed by infrared spectroscopy and total water contents were calculated using absorptivity coefficients for compositions extremely close to that investigated here. The variation of viscosity as a function of water content and temperature can be described in the high viscosity interval of relevance to many welding processes by the non-Arrhenian expression:

(1)

log₁₀ η=−5.900−0.286 ln (H₂O)+(10775.4−394.8(H₂O))/(T−148.7+21.65 ln (H₂O))

whereas the high viscosity range alone is adequately described by the Arrhenian expression

(2)

log₁₀ η=−10.622−0.738 ln (H₂O)+(17114.3−590.4(H₂O))×1/T

where η is the viscosity in Pa s, H₂O is the water content in wt% and T is the temperature in K.These results are particularly useful for the scaling of conditions extant during the welding of phonolitic products of Montaña Blanca. The welding of glassy phonolitic rocks is enhanced by the lower viscosity of these melts with respect to calcalkaline rhyolites. The ratio of viscosities of phonolitic to calcalkaline rhyolitic melts is a complex function of temperature and water content and reaches up to 10^4.5 at 0.1 wt% H₂O and 500°C. Abundant evidence of welding and remobilisation of pyroclastic and spatter products of Teide system volcanism are consistent with these experimental observations.     

Identification of Pathways for Hydrogen Gas Migration in Fault Zones with a Discontinuous,Heterogeneous Permeability Structure and the Relationship to Particle Size Distribution of Fault Materials

Previous studies have reported that high concentrations of H₂ gas are released from active fault zones. Experimental studies suggest that the H₂ gas is derived from the reaction of water with free radicals formed when silicate minerals are fractured at hypocenter depths during fault activities. However, the pathways for migration of deep-seated fluids to surface are still unknown. In this study we performed quick, multipoint H₂ gas measurements across a fault zone using a portable gas monitor and a hand drill. The fault zone studied includes a smectite-rich fault core dividing two clearly distinguishable damage zones: granite cataclasite and welded tuff fault breccia. The measurements show that H₂ gas emissions collected in 2–3 h sampling periods from start of measurement range from 320.3 to 446.2 ppm/min in the granite cataclasite and 60.5 to 137.8 ppm/min in the welded tuff fault breccias. Negligible quantities of H₂ gas could be collected from the fault core. Particle size distribution analyses of fault rocks indicate that the granite cataclasite tends to be rich in particles that are finer, i.e., less cohesive and easy to disaggregate, which leads to the inference that the granite cataclasite has high permeability. Based on the H₂ gas measurements and the particle size distribution analyses, the H₂ gas is considered to have migrated in permeable damage zones mostly by advection with groundwater. Multipoint H₂ gas measurement will be effective in qualitative delineation of variations in permeability of regional structures.     

Gasdynamic propagation of rocket exhaust products in the upper atmosphere

The dispersion of exhaust products of rocket fuel in the direction perpendicular to the motion of a rocket is investigated in this work. A comparison of the results of numerical calculations with a self-similar approximation of a strong cylindrically symmetric explosion is fulfilled. It is shown that at sufficiently high rocket velocity V _∞, which exceeds the sum of gas exhaust velocity V _e from the nozzle and sound speed V _s (V _∞ > V _e +V _s ), a gasdynamic hole can arise around the rocket trajectory in the upper atmosphere, inside which the total concentration of gas becomes less than the equilibrium concentration of gas at a given altitude. The dynamics of the profiles of density and temperature of the exhaust products inside a rocket plume is calculated.     

新疆呼图壁地下储气库断层气体地球化学特征研究

Rn、CO2、Hg、H2等断层气体被广泛应用于断层活动性以及断层结构特征的研究.当前,研究介质中压力变化与断层气间的关系是断层气映震研究的主要技术方法之一.新疆呼图壁地下储气库自建成以来,每年以周期性循环"注入/采出"模式运行,该运行模式带来的储气库气压变化会影响周围地区的地震活动.同时,这一定期加压存储与减压释放气体...     

Genetic features of gas-condensate reservoirs in the Kekeya Field,southwest depression in the Tarim Basin,China

Oils, condensates and natural gases in the Kekeya Field, southeast depression of the Tarim Basin were studied for their geochemical characteristics. According to the distribution analysis of the C₂/C₃ values with C₁/C₂ values, C₂/C₃ values with C₁/C₃ values, as well as C₂/C₃ values with dryness index, there are two different types of natural gases in the studied field, which are spatially regularly distributed. One is the oil cracking gas, located on shallow reservoirs over X ²₅ reservoir, namely Upper oil legs; the other is kerogen cracking gas, located on X ²₇ reservoirs, X₈ reservoirs and E₂ k reservoirs, namely Lower oil legs. In addition, the distribution patterns of molar concentration of oils and condensates with different carbon numbers of the n-alkanes in the Kekeya Field indicate that the crude oils have experienced several kinds of secondary alterations, which were closely related to the charging of gaseous hydrocarbons after petroleum accumulation. These results indicate that, based on the research of δ ¹³C values of individual hydrocarbons, heptane values and isoheptane values of light hydrocarbons and aromatic maturity parameters for oils, condensates and natural gases, oils and gases were charged at different geological time in the Kekeya Field.

     

Genetic features of gas-condensate reservoirs in the Kekeya Field,southwest depression in the Tarim Basin,China

Oils, condensates and natural gases in the Kekeya Field, southeast depression of the Tarim Basin were studied for their geochemical characteristics. According to the distribution analysis of the C₂/C₃ values with C₁/C₂ values, C₂/C₃ values with C₁/C₃ values, as well as C₂/C₃ values with dryness index, there are two different types of natural gases in the studied field, which are spatially regularly distributed. One is the oil cracking gas, located on shallow reservoirs over X ₅ ² reservoir, namely Upper oil legs; the other is kerogen cracking gas, located on X ₇ ² reservoirs, X₈ reservoirs and E₂ k reservoirs, namely Lower oil legs. In addition, the distribution patterns of molar concentration of oils and condensates with different carbon numbers of the n-alkanes in the Kekeya Field indicate that the crude oils have experienced several kinds of secondary alterations, which were closely related to the charging of gaseous hydrocarbons after petroleum accumulation. These results indicate that, based on the research of δ ¹³C values of individual hydrocarbons, heptane values and isoheptane values of light hydrocarbons and aromatic maturity parameters for oils, condensates and natural gases, oils and gases were charged at different geological time in the Kekeya Field.     

Erta'ale lava lake: heat and gas transfer to the atmosphere

Data on uncontaminated samples of volcanic gases can be counted on the fingers of one hand, yet estimation of total volcanic gas flow cannot be made without such data. In this paper the flux of gas from the lava lake to the atmosphere is calculated by a heat budget based on the excess heat loss caused by combustion of H₂ and CO and by the mass rate of loss of other gases on the basis of their ratios to H₂ and CO in the unoxidized gas samples. The estimated rates of loss of H₂O, CO₂, SO₂ and HCl are consistent with the rate of loss of heat if this heat is generated by crystallization and if the initial magma contains concentrations of gas appropriate for submarine basalt from oceanic ridges. The moderate activity of permanent degassing from the two active lava ponds studied gives a lower flux than that of other volcanoes.     

Hydropower – A Green Energy? Tropical Reservoirs and Greenhouse Gas Emissions

Reservoirs are man‐made lakes that severely impact on river ecosystems, and in addition, the new lake ecosystem can be damaged by several processes. Thus, the benefits of a reservoir, including energy production and flood control, must be measured against their impact on nature. New investigations point out that shallow and tropical reservoirs have high emission rates of the greenhouse gases CO₂ and CH₄. The methane emissions contribute strongly to climate change because CH₄ has a 25 times higher global warming potential than CO₂. The pathways for its production include ebullition, diffuse emission via the water‐air interface, and degassing in turbines and downstream of the reservoir in the spillway and the initial river stretch. Greenhouse gas emissions are promoted by a eutrophic state of the reservoir, and, with higher trophic levels, anaerobic conditions occur with the emission of CH₄. This means that a qualitative and quantitative jump in greenhouse gas emissions takes place. Available data from Petit Saut, French Guinea, provides a first quantification of these pathways. A simple evaluation of the global warming potential of a reservoir can be undertaken using the energy density, the ratio of the reservoir surface and the hydropower capacity; this parameter is mainly determined by the reservoir's morphometry but not by the hydropower capacity. Energy densities of some reservoirs are given and it is clearly seen that some reservoirs have a global warming potential higher than that of coal use for energy production.