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1.
<正>Zabuye Salt Lake in Tibet,China is a carbonate-type salt lake,which has some unique characteristics that make it different from other types of salt lakes.The lake is at the latter period in its evolution and contains liquid and solid resources.Its brine is rich in Li,B,K and other useful minor elements that are of great economic value.We studied the concentration behavior of these elements and the crystallization paths of salts during isothermal evaporation of brine at 15℃and 25℃.The crystallization sequence of the primary salts from the brine at 25℃is halite(NaCl)→aphthitalite (3K_2SO_4·Na_2SO_4)→zabuyelite(Li_2CO_3)→trona(Na_2CO_3·NaHCO_3·2H_2O)→thermonatrite (Na_2CO_3·H_2O)→sylvite(KCl),while the sequence is halite(NaCl)→sylvite(KCl)→trona (Na_2CO_3·NaHCO_3·2H_2O)→zabuyelite(Li_2CO_3)→thermonatrite(Na_2CO_3·H_2O)→aphthitalite (3K_2SO_4·Na_2SO_4) at 15℃.They are in accordance with the metastable phase diagram of the Na~+,K~+-Cl~-, CO_3~(2-),SO_4~(2-)-H_2O quinary system at 25℃,except for Na_2CO_3·7H_2O which is replaced by trona and thermonatrite.In the 25℃experiment,zabuyelite(Li_2CO_3) was precipitated in the early stage because Li_2CO_3 is supersaturated in the brine at 25℃,in contrast with that at 15℃,it precipitated in the later stage.Potash was precipitated in the middle and late stages in both experiments,while boron was concentrated in the early and middle stages and precipitated in the late stage.  相似文献   

2.
The Kalatongke Cu–Ni sulfide deposits located in the East Junggar terrane, northern Xinjiang, western China are the largest magmatic sulfide deposits in the Central Asian Orogenic Belt (CAOB). The chemical and carbon isotopic compositions of the volatiles trapped in olivine, pyroxene and sulfide mineral separates were analyzed by vacuum stepwise-heating mass spectrometry. The results show that the released volatiles are concentrated at three temperature intervals of 200–400°C, 400–900°C and 900–1200°C. The released volatiles from silicate mineral separates at 400–900°C and 900–1200°C have similar chemical and carbon isotopic compositions, which are mainly composed of H2O (av. ~92 mol%) with minor H2, CO2, H2S and SO2, and they are likely associated with the ore-forming magmatic volatiles. Light δ13CCO2 values (from ?20.86‰ to ?12.85‰) of pyroxene indicate crustal contamination occurred prior to or synchronous with pyroxene crystallization of mantle-derived ore-forming magma. The elevated contents of H2 and H2O in the olivine and pyroxene suggest a deep mantle-originated ore-forming volatile mixed with aqueous volatiles from recycled subducted slab. High contents of CO2 in the ore-forming magma volatiles led to an increase in oxygen fugacity, and thereby reduced the solubility of sulfur in the magma, then triggered sulfur saturation followed by sulfide melt segregation; CO2 contents correlated with Cu contents in the whole rocks suggest that a supercritical state of CO2 in the ore-forming magma system under high temperature and pressure conditions might play a key role in the assemblage of huge Cu and Ni elements. The volatiles released from constituent minerals of intrusion 1# have more CO2 and SO2 oxidized gases, higher CO2/CH4 and SO2/H2S ratios and lighter δ13CCO2 than those of intrusions 2# and 3#. This combination suggests that the higher oxidation state of the volatiles in intrusion 1# than intrusions 2# and 3#, which could be one of key ore-forming factors for large amounts of ores and high contents of Cu and Ni in intrusion 1#. The volatiles released at 200–400°C are dominated by H2O with minor CO2, N2+CO and SO2, with δ13CCO2 values (?25.66‰ to ?22.98‰) within the crustal ranges, and are considered to be related to secondary tectonic– hydrothermal activities.  相似文献   

3.
The Quaternary was the main evaporite deposition period in the Qaidam Basin (QB), but the correlation between the evaporite deposition period and the glacial period is still unclear. In this study, the research objects are primarily evaporite-bearing strata in a 461.58 m-long drill core in the QB. X-ray powder diffraction (XRD) and scanning electron microscopy (SEM) were applied to study the evaporite minerals, U-Th dating being applied to construct the 230Th geochronological framework. Evaporite deposition from Marine Isotope Stage (MIS) 15 to MIS 4 in the borehole was reconstructed via mineralogical and geochronological data. The evaporite minerals are mainly halite (NaCl), mirabilite (Na2SO4·10H2O), thenardite (Na2SO4) and gypsum (CaSO4·2H2O). A total of 9 effective 230Th data points, ranging from 492.5 ± 43.0 ka to 62.0 ± 11.9 ka, were obtained. The depositional age of the earliest halite layer in the borehole is 592.5–563.0 ka. There were mirabilite deposits in the QB during the cold glacial environment of MIS 6. During MIS 4, the study area desiccated, with mirabilite and halite being deposited. This study suggests that mirabilite is an indicator mineral for the glacial environment in the QB, while halite deposition does not correspond well to glaciation.  相似文献   

4.
The Dayingezhuang gold deposit, hosted mainly by Late Jurassic granitoids on Jiaodong Peninsula in eastern China, contains an estimated 170 t of gold and is one of the largest deposits within the Zhaoping fracture zone. The orebodies consist of auriferous altered pyrite–sericite–quartz granites that show Jiaojia-type (i.e., disseminated and veinlet) mineralization. Mineralization and alteration are structurally controlled by the NE- to NNE-striking Linglong detachment fault. The mineralization can be divided into four stages: (K-feldspar)–pyrite–sericite–quartz, quartz–gold–pyrite, quartz–gold–polymetallic sulfide, and quartz–carbonate, with the majority of the gold being produced in the second and third stages. Based on a combination of petrography, microthermometry, and laser Raman spectroscopy, three types of fluid inclusion were identified in the vein minerals: NaCl–H2O (A-type), CO2–H2O–NaCl (AC-type), and pure CO2 (PC-type). Quartz crystals in veinlets that formed during the first stage contain mainly AC-type fluid inclusions, with rare PC-type inclusions. These fluid inclusions homogenize at temperatures of 251°C–403°C and have low salinities of 2.2–9.4 wt% NaCl equivalent. Quartz crystals that formed in the second and third stages contain all three types of fluid inclusions, with total homogenization temperatures of 216°C–339°C and salinities of 1.8–13.8 wt% NaCl equivalent for the second stage and homogenization temperatures of 195°C–321°C and salinities of 1.4–13.3 wt% NaCl equivalent for the third stage. In contrast, quartz crystals that formed in the fourth stage contains mainly A-type fluid inclusions, with minor occurrences of AC-type inclusions; these inclusions have homogenization temperatures of 106°C–287°C and salinities of 0.5–7.7 wt% NaCl equivalent. Gold in the ore-forming fluids may have changed from Au(HS)0 as the dominant species under acidic conditions and at relatively high temperatures and fO2 in the early stages, to Au(HS)2– under neutral-pH conditions at lower temperatures and fO2 in the later stages. The precipitation of gold and other metals is inferred to be caused by a combination of fluid immiscibility and water–rock interaction.  相似文献   

5.
Calcite cements are volumetrically dominant among the most diagenetic constituents in turbidite sandstones of the Paleogene Shahejie Formation in the Dongying Depression. The results show carbonate cements mainly occur in three phases: Calcite I (pre-compaction), Calcite II (post-compaction) and ankerite in the turbidite sandstone. The isotopic composition of Calcite I and Calcite II range from ?4.3‰ to 4.4‰, ?3.5‰ to 4.3‰ PDB, respectively, suggesting that the calcite cements are mainly derived from the interbedded shales. The early calcite cement precipitated from the mixing of lacustrine and meteoric waters at 38–69°C. The late-phase calcite precipitated from pore waters modified by water-rock interactions at 64–126°C. Two distribution patterns of calcite cements can be identified, depending on their position within the sandstone. The peripheral cementation of the sandstones is near the sand-shale contact. The development of cement is controlled by sandstone thickness and the properties of the interbedded shale. For scattered cementation, the distribution of the calcite cement is not controlled by the sand-shale contact. Calcite cement was preferentially distributed in coarse-grained sandstones, indicating that sandstones with high original permeability are the preferred pathway for the migration of early diagenetic fluids.  相似文献   

6.
Character of the Si and Al Phases in Coal Gangue and Its Ash   总被引：1，自引：0，他引：1  
Abstract: Analysis of the Si and Al phases in coal gangue fuel and its ash is important for use of coal gangue ashes. A comprehensive study by theoretical and experimental analyses with differential thermal analysis, X-ray diffraction and Infrared Spectroscopy has been made in the present article to explore the diagram of the Si and Al phases in coal gangue fuel and its ashes. It is found that kaolinite and quartz are the main phases in coal gangue fuel. The ratio of moles Al2O3 to SiO2 (i.e., Al2O3 (mole) /SiO2 (mole)) is usually no more than 0.5 in most coal gangue fuel and its ashes. The kaolinit at about 984°C releases a large quantity of SiO2, which makes calcine coal gangue more active than coal gangue itself. The relationship between the ratio Al2O3 (mole)/SiO2(mole) and the components of coal gangue ash is analyzed, resulting in a formula to calculate the quantity of each phase. Applying the formula to the testing samples from an electric plant in north China supports the above conclusions.  相似文献   

7.
The high-pressure (HP) eclogite in the western Dabie Mountain encloses numerous hornblendes, mostly barroisite. Opinions on the peak metamorphic P-T condition, PT path and mineral paragenesis of it are still in dispute. Generally, HP eclogite involves garnet, omphacite, hornblendes and quartz, with or without glaucophane, zoisite and phengite. The garnet has compositional zoning with XMg increase, XCa and XMn decrease from core to rim, which indicates a progressive metamorphism. The phase equilibria of the HP eclogite modeled by the P-T pseudosection method developed recently showed the following: (1) the growth zonation of garnet records a progressive metamorphic PT path from pre-peak condition of 1.9–2.1 GPa at 508°C–514°C to a peak one of 2.3–2.5 GPa at 528°C–531°C for the HP eclogite; (2) the peak mineral assemblage is garnet+omphacite+glaucophane+quartz±phengite, likely paragenetic with lawsonite; (3) the extensive hornblendes derive mainly from glaucophane, partial omphacite and even a little garnet due to the decompression with some heating during the post-peak stage, mostly representing the conditions of about 1.4–1.6 GPa and 580°C–640°C, and their growth is favored by the dehydration of lawsonite into zoisite or epidote, but most of the garnet, omphacite or phengite in the HP eclogite still preserve their compositions at peak condition, and they are not obviously equilibrious with the hornblendes.  相似文献   

8.
The uncertainty surrounding the thermal regimes of the ultra-deep strata in the Tarim and Sichuan basins, China, is unfavorable for further hydrocarbon exploration. This study summarizes and contrasts the present-day and paleo heat flow, geothermal gradient and deep formation temperatures of the Tarim and Sichuan basins. The average heat flow of the Tarim and Sichuan basins are 42.5 ± 7.6 mW/m2 and 53.8 ± 7.6 mW/m2, respectively, reflecting the characteristics of ‘cold’ and ‘warm’ basins. The geothermal gradient with unified depths of 0–5,000 m, 0–6,000 m and 0–7,000 m in the Tarim Basin are 21.6 ± 2.9 °C/km, 20.5 ± 2.8 °C/km and 19.6 ± 2.8 °C/km, respectively, while the geothermal gradient with unified depths of 0–5,000 m, 0–6,000m and 0–7,000 m in the Sichuan Basin are 21.9 ± 2.3 °C/km, 22.1 ± 2.5 °C/km and 23.3 ± 2.4 °C/km, respectively. The differential change of the geothermal gradient between the Tarim and Sichuan basins with depth probably results from the rock thermal conductivity and heat production rate. The formation temperatures at depths of 6,000 m, 7,000 m, 8,000 m, 9,000 m and 10,000 m in the Tarim Basin are 80°C–190°C, 90°C–220°C, 100°C–230°C, 110°C–240°C and 120°C–250°C, respectively, while the formation temperatures at depths of 6,000 m, 7,000 m, 8,000 m and 9,000 m in the Sichuan Basin are 120°C–200°C, 140°C–210°C, 160°C–260°C and 180°C–280°C, respectively. The horizontal distribution pattern of the ultra-deep formation temperatures in the Tarim and Sichuan basins is mainly affected by the basement relief, fault activity and hydrothermal upwelling. The thermal modeling revealed that the paleo-heat flow in the interior of the Tarim Basin decreased since the early Cambrian with an early Permian abrupt peak, while that in the Sichuan Basin experienced three stages of steady state from Cambrian to early Permian, rapidly rising at the end of the early Permian and declining since the late Permian. The thermal regime of the Sichuan Basin was always higher than that of the Tarim Basin, which results in differential oil and gas generation and conservation in the ultra-deep ancient strata. This study not only promotes theoretical development in the exploration of ultra-deep geothermal fields, but also plays an important role in determining the maturation phase of the ultra-deep source rocks and the occurrence state of hydrocarbons in the Tarim and Sichuan basins.  相似文献   

9.
Liquid–liquid immiscibility has crucial influences on geological processes, such as magma degassing and formation of ore deposits. Sulfate, as an important component, associates with many kinds of deposits. Two types of immiscibility, including (i) fluid–melt immiscibility between an aqueous solution and a sulfate melt, and (ii) fluid–fluid immiscibility between two aqueous fluids with different sulfate concentrations, have been identified for sulfate–water systems. In this study, we investigated the immiscibility behaviors of a sulfate- and quartz-saturated Na2SO4–SiO2–H2O system at elevated temperature, to explore the phase relationships involving both types of immiscibility. The fluid–melt immiscibility appeared first when the Na2SO4–SiO2–H2O sample was heated to ~270°C, and then fluid–fluid immiscibility emerged while the sample was further heated to ~450°C. At this stage, the coexistence of one water-saturated sulfate melt and two aqueous fluids with distinct sulfate concentrations was observed. The three immiscible phases remain stable over a wide pressure–temperature range, and the appearance temperature of the fluid–fluid immiscibility increases with the increased pressure. Considering that sulfate components occur extensively in carbonatite-related deposits, the fluid–fluid immiscibility can result in significant sulfate fractionation and provides implications for understanding the formation of carbonatite-related rare earth deposits.  相似文献   

10.
Studies of the mantle-derived iherzolites from Nushan show that in addition to CO2,there were present H2O and small amounts of CO, CH4, SO2,Cl and F in the initial mantlc fluids derived fron the asthenospheric mantlc plumc .The imitial fluids accumulated in some regions of the mantle, resulting in lowering of the mantle solidus (and liquidus) and partial melting of the upper mantle. Melts formed from low-degree of fluid-involved partial melting of the upper mantle would be highly enriched in incompatible elements.Fluies and melts are allthe metasomatic agents for mantle metasomatism, and the interaction between them and the depleted mantle could result in the substan-tial local enrichment of LREE and incompatible elements in the latter.In case that the concentration of H2O in the fluids (and melts) is lower ,only cryptic metasomatism would occur, in case that the concentration of H2O is higher,the degree of partial melting would be higher and hydrous metasomatic phases(e.g. amphiboles )would nucleate. Under such circumstances, there would occur model metasomatism.  相似文献   

11.
Carbonatites from the Oldoinyo Lengai volcano, northern Tanzania, are unstable under normal atmospheric conditions. Owing to carbonatite interaction with water, the major minerals—gregoryite Na2(CO3), nyerereite Na2Ca(CO3)2, and sylvite KCl—are dissolved and replaced with secondary low-temperature minerals: thermonatrite Na2(CO3) · H2O, trona Na3(CO3)(HCO3) · 2H2O, nahcolite Na(HCO3), pirssonite Na2Ca(CO3)2 · 2H2O, calcite Ca(CO3), and shortite Na2Ca2(CO3)3. Thermodynamic calculations show that the formation of secondary minerals in Oldoinyo Lengai carbonatites are controlled by the pH of the pore solution, H2O and CO2 fugacity, and the ratio of Ca and Na activity in the Na2O–CaO–CO2–H2O system.  相似文献   

12.
Lake Kitagata, Uganda, is a hypersaline crater lake with Na–SO4–Cl–HCO3–CO3 chemistry, high pH and relatively small amounts of SiO2. EQL/EVP, a brine evaporation equilibrium model (Risacher and Clement 2001), was used to model the major ion chemistry of the evolving brine and the order and masses of chemically precipitated sediments. Chemical sediments in a 1.6-m-long sediment core from Lake Kitagata occur as primary chemical mud (calcite, magadiite [NaSi7O13(OH)3·3H2O], burkeite [Na6(CO3)(SO4)2]) and as diagenetic intrasediment growths (mirabilite (Na2SO4·10H2O)). Predicted mineral assemblages formed by evaporative concentration were compared with those observed in salt crusts along the shoreline and in the core from the lake center. Most simulations match closely with observed natural assemblages. The dominant inflow water, groundwater, plays a significant role in driving the chemical evolution of Lake Kitagata water and mineral precipitation sequences. Simulated evaporation of Lake Kitagata waters cannot, however, explain the large masses of magadiite found in cores and the formation of burkeite earlier in the evaporation sequence than predicted. The masses and timing of formation of magadiite and burkeite may be explained by past groundwater inflow with higher alkalinity and SiO2 concentrations than exist today.  相似文献   

13.
《Applied Geochemistry》1999,14(1):53-65
Owens Lake in SE California became essentially dry by the 1920s after the Los Angeles Aqueduct was constructed and diversion of water from the Owens River began. Frequent dust storms at Owens Lake produce clouds of efflorescent salts which present human health hazards as a result of their small particle size and elevated concentrations of As and SO4. This study was conducted to characterize the evolution of major elements in ground water in eastern Owens Lake and to examine the factors controlling the concentrations of dissolved As and F. Evapoconcentration of shallow ground waters at the lakebed surface produces high pH, high alkalinity brines with major ion compositions that are consistent with those predicted by the Hardie–Eugster Model. Evaporite minerals identified in the surface salts using XRD were halite (NaCl), thenardite (Na2SO4), trona (Na3H(CO3)2·2H2O), pirssonite (Na2Ca(CO3)2·2H2O), and nesquehonite (MgCO3·3H2O). Significant correlations between both As and F with Li in shallow ground waters indicate that As and F are not partitioned into surface salts until very high salinities are reached (>9.0 m). Leaching experiments show that As and F can be readily released from lakebed salts when exposed to natural precipitation. Conservative behavior of As and F results from the high pH values and low Ca activities of shallow ground waters that contribute to: (1) redox stability of As(V) even at moderately reducing conditions, (2) a decrease in the adsorption affinities of As and F to mineral surfaces, (3) undersaturation with respect to fluorite (CaF2(s)).  相似文献   

14.
Brine extremely rich in potassium, boron and bromine has been discovered from the Middle Triassic Leikoupo Formation at a depth of 4300 m in Sichuan Province. It contains ～50 g/L of K+, >92 g/L of Na+, >12 g/L of B2O3, >2.36 g/L of Br? and ～0.030 g/L of I+. The solid precipitates during evaporation at 25°C include KB5O8·4H2O, K2B4O7·3H2O, MgCl2·6H2O and KMgCl3·6H2O. The brine ranges from 2.2‰ to 2.8‰ (SMOW) in δ18O, ? 38‰ – ? 53‰ (SMOW) in δD, 15.6‰ in δ34S, and 13.5‰–15.1‰ in δ11B. These data, particularly the isotopic composition of boron, indicate that the brine has a composite derivation from marine and nonmarine brines and dissolved marine evaporites in the Triassic system.  相似文献   

15.
The ion-interaction model of PITZER (1973), is very effective in deriving stability relationships at high concentrations for the system Na-Cl-HCO3-CO3-OH-H2O. The solubility products of the main sodium carbonates have been calculated from solubility data between 5 and 50°C. The stability diagram in log pco2 — temperature coordinates and the invariant points deduced from the newly determined data are in good agreement with the most recent measurements.These results are used to calculate the activities of the major dissolved species in Lake Magadi brines (Kenya). The thermodynamic treatment confirms the main conclusions reached earlier by Eugster (1970, 1980) mainly from field observations. Trona precipitation occurs at equilibrium while natron is likely to form when the temperature decreases below 25°C. After the salt deposition the CO2 supply from the atmosphere is too slow to allow equilibrium between the atmosphere and the brines. In the next stages of evaporative concentration thermonatrite and halite precipitate. The deposition of the latter salts along with the observed HCO?3 depletion suggest that fractional crystallization is likely to control trona deposition.  相似文献   

16.
The thermal stability of sideronatrite, ideally Na2Fe3+(SO4)2(OH)·3(H2O), and its decomposition products were investigated by combining thermogravimetric and differential thermal analysis, in situ high-temperature X-ray powder diffraction (HT-XRPD) and Fourier transform infrared spectroscopy (HT-FTIR). The data show that for increasing temperature there are four main dehydration/transformation steps in sideronatrite: (a) between 30 and 40 °C sideronatrite transforms into metasideronatrite after the loss of two water molecules; both XRD and FTIR suggest that this transformation occurs via minor adjustments in the building block. (b) between 120 and 300 °C metasideronatrite transforms into metasideronatrite II, a still poorly characterized phase with possible orthorhombic symmetry, consequently to the loss of an additional water molecule; X-ray diffraction data suggest that metasideronatrite disappears from the assemblage above 175 °C. (c) between 315 and 415 °C metasideronatrite II transforms into the anhydrous Na3Fe(SO4)3 compound. This step occurs via the loss of hydroxyl groups that involves the breakdown of the [Fe3+(SO4)2(OH)] ∞ 2? chains and the formation of an intermediate transient amorphous phase precursor of Na3Fe(SO4)3. (d) for T > 500 °C, the Na3Fe(SO4)3 compound is replaced by the Na-sulfate thenardite, Na2SO4, plus Fe-oxides, according to the Na3Fe3+(SO4)3 → 3/2 Na2(SO4) + 1/2 Fe2O3 + SOx reaction products. The Na–Fe sulfate disappears around 540 °C. For higher temperatures, the Na-sulfates decomposes and only hematite survives in the final product. The understanding of the thermal behavior of minerals such as sideronatrite and related sulfates is important both from an environmental point of view, due to the presence of these phases in evaporitic deposits, soils and sediments including extraterrestrial occurrences, and from the technological point of view, due to the use of these materials in many industrial applications.  相似文献   

17.
《Chemical Geology》2006,225(3-4):256-265
SeO42− ions can substitute for sulphate in the gypsum structure. In this work crystals of different Ca(SO4,SeO4)·2H2O solid solutions were precipitated by mixing a CaCl2 solution with solutions containing different ratios of Na2SO4 and Na2SeO4. The compositions of the precipitates were analysed by EDS and the cell parameters were determined by X-ray powder diffraction. Moreover, a comparative study on dehydration behaviour of selenate rich and sulfate rich Ca(SO4,SeO4)·2H2O solid solutions was carried out by thermogravimetry.The experimental results show that the Ca(SO4,SeO4)·2H2O solid solution presents a symmetric miscibility gap for compositions ranging from XCaSO4·2H2O = 0.23 to XCaSO4·2H2O = 0.77. By considering a regular solution model a Guggenheim parameter a0 = 2.238 was calculated. The solid phase activity coefficients obtained with this parameter were used to calculate a Lippmann diagram for the system Ca(SO4,SeO4)·2H2O–H2O.  相似文献   

18.
A new microscope vacuum heating stage and gas analyzer has been developed for measurement of H2O, CO2, SO2, and noncondensable gas (H2, CO, N2, Ar, CH4, etc.) evolved from samples, particularly natural glass, at temperatures up to 1280°C. The gas evolved upon heating to 1280δC is collected in a liquid nitrogen cold trap. Gas components are identified by the characteristic vapor pressure and temperature ranges over which solid and vapor are in equilibrium during sublimation of individual components. The masses of CO2, SO2, and H2O derived from samples and blanks are calculated using the ideal gas law, the molecular weights of the components, and the gauge constant (i.e. the ratio of the number of moles of a gas to its partial pressure in the constant volume). Results obtained by repeated determinations of H2O, CO2, and SO2 evolved from a submarine basaltic glass from Kilauea volcano, Hawaii, (average sample mass = 3 × 10?3 g) gave probable errors for the determinations of H2O (0.23%), CO2 (0.025%), and S (0.071%) equal to 4, 10, and 8% respectively, of the concentrations. Determinations of H2O in smaller samples of H2O-poor basaltic pumice show a linear proportionality (0.063%) between the measured H2O and the sample mass over the range 0.1 × 10?6 to 1.7 × 10?6 g H2O. Comparisons of H2O determinations by this technique with those obtained by Penfield, gas chromatic, microcoulometric, and vacuum fusion techniques used elsewhere show reasonably good agreement. Determinations of SO2 by this technique agree reasonably well X-ray fluorescence and electron microprobe determinations of sulfur. Determinations of CO2 by the present technique are reproducible but cannot be compared directly to measurements made in other labs because of differences in samples analyzed. The principle advantages of this analytical technique are the very small sample required, the simultaneous determination of H2O, CO2, SO2 and noncondensable gas, the avoidance of calibration procedures dependent on chemical standards, and the visual observations that can be made during sample outgassing.  相似文献   

19.
Perennial ice covers on many Antarctic lakes have resulted in high lake inorganic carbon contents. The objective of this paper was to evaluate and compare the brine and CO2 chemistries of Lake Vida (Victoria Valley) and West Lake Bonney (Taylor Valley), two lakes of the McMurdo Dry Valleys (East Antarctica), and their potential consequences during global warming. An existing geochemical model (FREZCHEM-15) was used to convert measured molarity into molality needed for the FREZCHEM model, and this model added a new algorithm that converts measured DIC into carbonate alkalinity needed for the FREZCHEM model. While quite extensive geochemical information exists for ice-covered Taylor Valley lakes, such as West Lake Bonney, only limited information exists for the recently sampled brine of >25 m ice-thick Lake Vida. Lake Vida brine had a model-calculated pCO2 = 0.60 bars at the field pH (6.20); West Lake Bonney had a model-calculated pCO2 = 5.23 bars at the field pH (5.46). Despite the high degree of atmospheric CO2 supersaturation in West Lake Bonney, it remains significantly undersaturated with the gas hydrate, CO2·6H2O, unless these gas hydrates are deep in the sediment layer or are metastable having formed under colder temperatures or greater pressures. Because of lower temperatures, Lake Vida could start forming CO2·6H2O at lower pCO2 values than West Lake Bonney; but both lakes are significantly undersaturated with the gas hydrate, CO2·6H2O. For both lakes, simulation of global warming from current subzero temperatures (?13.4 °C in Lake Vida and ?4.7 °C in West Lake Bonney) to 10 °C has shown that a major loss of solution-phase carbon as CO2 gases and carbonate minerals occurred when the temperatures rose above 0 °C and perennial ice covers would disappear. How important these Antarctic CO2 sources will be for future global warming remains to be seen. But a recent paper has shown that methane increased in atmospheric concentration due to deglaciation about 10,000 years ago. So, CO2 release from ice lakes might contribute to atmospheric gases in the future.  相似文献   

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