Criteria for the recognition of acid-precipitated halite

Modern acid and neutral saline lakes in Western Australia are an excellent natural laboratory for testing how pH affects halite, and for developing criteria for distinguishing past acid saline waters from past neutral saline waters in the rock record. This study characterizes and compares physical, chemical and biological features in halite precipitated from acid (pH 1·7 to 4·2) and neutral (pH 6·8 to 7·3) saline lakes in southern Western Australia. Supplemental data include synthetic halite grown from acid and neutral saline solutions, as well as halite deposited in Permian acid lakes. Although physical processes of halite growth are not affected by pH, there are differences in the colour, accessory minerals, fluid inclusions and microfossils between acid and neutral halites. Acid lake halite commonly is yellow or orange in colour; neutral lake halites examined in this study are always snow white. Acid halites tend to contain abundant sulphate and iron oxide minerals, both as solid inclusions and as solids within fluid inclusions; neutral halites contain little, if any, sulphates and no iron oxides. Acid fluid inclusion freezing/melting behaviours include characteristics that differ from neutral fluid inclusion behaviours, such as lower eutectic temperatures, higher and wider temperature range of hydrohalite rims with a definable fuzzy border and more complex metastable phases. Acid halite contains 'hairy blobs', clusters of bacterial/archaeal/fungal remains and sulphate crystals, which are not found in halite from neutral lakes. This distinct assemblage of features characteristic of modern acid lake halites may serve as informal criteria for the recognition of past acid lake evaporites in the rock record.     

柴达木盆地西部中更新世气候转型期的古水温:来自SG-1钻孔石盐流体包裹体的证据

中更新世气候转型事件(MPT)是全球性冷气候事件,在柴达木盆地也有记录,但关于该事件形成时的古温度数据较少。石盐原生流体包裹体形成于浅水环境,其均一温度可直接反映晶体形成时的卤水温度,是恢复古温度常用的指标之一。本文选择柴达木盆地西部钻孔SG-1中1.22~0.88 Ma期间的石盐晶体进行流体包裹体均一温度测试,共获得390个石盐流体包裹体数据。其均一温度最高为50 ℃,最低为6.8 ℃,90%以上温差值在10 ℃以内,且石盐流体包裹体大小与温度没有明显线性相关关系,这说明SG-1钻孔石盐流体包裹体被捕获后没有受到后期热液的改造。均一温度数据反映了石盐沉积时的古水温特征。石盐晶体主要在暖季析出,原生流体包裹体恢复的古水温可能是暖季节的温度。均一温度的最高值可能受到热液和气候的共同作用。MPT时期,石盐流体包裹体均一温度(中位值T_h,med)接近于现代盆地7月份大气温度的平均值,高于盆地的全年温度及MPT时期的全球气温,与MPT时期地中海的海水表面温度相当,均一温度的平均值(T_h,avg)高于以上温度。SG-1钻孔记录的柴达木盆地MPT事件最冷期出现在约1.165~1.0 Ma。     

U-Series Chronology of Lacustrine Deposits in Death Valley, California

Uranium-series dating on a 186-m core (DV93-1) drilled from Badwater Basin in Death Valley, California, and on calcareous tufas from nearby strandlines shows that Lake Manly, the lake that periodically flooded Death Valley during the late Pleistocene, experienced large fluctuations in depth and chemistry over the last 200,000 yr. Death Valley has been occupied by a long-standing deep lake, perennial shallow saline lakes, and a desiccated salt pan similar to the modern valley floor. The average sedimentation rate of about 1 mm/yr for core DV93-1 was punctuated by episodes of more-rapid accumulation of halite. Arid conditions similar to the modern conditions prevailed during the entire Holocene and between 120,000 and 60,000 yr B.P. From 35,000 yr B.P. to the beginning of the Holocene, a perennial saline lake existed, over 70 m at its deepest. A much deeper and longer lasting perennial Lake Manly existed from about 185,000 to 128,000 yr B.P., with water depths reaching about 175 m, if not 330 m. This lake had two significant “dry” excursions of 10²–10³yr duration about 166,000 and 146,000 yr B.P., and it began to shrink to the point of halite precipitation between 128,000 and 120,000 yr B.P. The two perennial lake periods correspond to marine oxygen isotopic stages (OIS) 2 and 6. Based on the shoreline tufa ages, we do not rule out the possible existence 200,000 yr ago of yet a third perennial lake comparable in size to the OIS 6 lake. The²³⁴U/²³⁸U data suggest that U in tufa owes its origin mainly to Ca-rich springs fed by groundwater that emanated along lake shorelines in southern Death Valley, and that an increase of this spring-water input relative to the river-water input apparently occurred during OIS 6.     

Fluid Inclusions in Surface‐temperature Halite: Sample Preparation and Application

Paleo-temperature and paleo-environment can be interpreted from measuring homogenization temperatures of fluid inclusions within halite. In order to conduct such measurements, vapor bubbles within low-temperature fluid inclusion often need to be created through cooling process by using cooling stage or freezer. Proper cooling is critical for interpreting measured temperature data. We tested two common cooling methods, using heating/freezing stage and freezer, for studying fluid inclusions in halite precipitated in laboratory at conrtolled temperature of 25℃. While using the heating/freezing stage, halite samples were kept at-18℃ for 40–50 min; whereas for freezer, samples were stored at-18℃ for 1, 10, 20 and 40 days, respectively. By comparing the homogenization temperatures of the two cooling processes, we explored the detailed experimental processes and developed an optimal cooling nucleation procedure for homogenization temperature analyses of fluid inclusions within surface-temperature halite. The results show that the maximum homogenization temperatures from both methods approximate the actual brine temperature of 25℃. However, extended refrigeration time has noticeable influence on the results. The refrigeration time of the experiment can be shortened to meet requirements.     

Carbonatite melt–CO2 fluid inclusions in mantle xenoliths from Tenerife, Canary Islands: a story of trapping, immiscibility and fluid–rock interaction in the upper mantle

Three types of fluid inclusions have been identified in olivine porphyroclasts in the spinel harzburgite and lherzolite xenoliths from Tenerife: pure CO₂ (Type A); carbonate-rich CO₂–SO₂ mixtures (Type B); and polyphase inclusions dominated by silicate glass±fluid±sp±silicate±sulfide±carbonate (Type C). Type A inclusions commonly exhibit a “coating” (a few microns thick) consisting of an aggregate of a platy, hydrous Mg–Fe–Si phase, most likely talc, together with very small amounts of halite, dolomite and other phases. Larger crystals (e.g. (Na,K)Cl, dolomite, spinel, sulfide and phlogopite) may be found on either side of the “coating”, towards the wall of the host mineral or towards the inclusion center. These different fluids were formed through the immiscible separations and fluid–wall-rock reactions from a common, volatile-rich, siliceous, alkaline carbonatite melt infiltrating the upper mantle beneath the Tenerife. First, the original siliceous carbonatite melt is separated from a mixed CO₂–H₂O–NaCl fluid and a silicate/silicocarbonatite melt (preserved in Type A inclusions). The reaction of the carbonaceous silicate melt with the wall-rock minerals gave rise to large poikilitic orthopyroxene and clinopyroxene grains, and smaller neoblasts. During the metasomatic processes, the consumption of the silicate part of the melt produced carbonate-enriched Type B CO₂–SO₂ fluids which were trapped in exsolved orthopyroxene porphyroclasts. At the later stages, the interstitial silicate/silicocarbonatite fluids were trapped as Type C inclusions. At a temperature above 650 °C, the mixed CO₂–H₂O–NaCl fluid inside the Type A inclusions were separated into CO₂-rich fluid and H₂O–NaCl brine. At T<650 °C, the residual silicate melt reacted with the host olivine, forming a reaction rim or “coating” along the inclusion walls consisting of talc (or possibly serpentine) together with minute crystals of NaCl, KCl, carbonates and sulfides, leaving a residual CO₂ fluid. The homogenization temperatures of +2 to +25 °C obtained from the Type A CO₂ inclusions reflect the densities of the residual CO₂ after its reactions with the olivine host, and are unrelated to the initial fluid density or the external pressure at the time of trapping. The latter are restricted by the estimated crystallization temperatures of 1000–1200 °C, and the spinel lherzolite phase assemblage of the xenolith, which is 0.7–1.7 GPa.     

Marine-like potash evaporite formation on a continental playa: case study from Chott el Djerid, southern Tunisia

An exceptional flood in January 1990 led to the formation of a large ephemeral lake on the Chott el Djerid, a salt playa in southern Tunisia. Repeated observations made during 1990 show that the ephemeral lake underwent four evolutionary stages: (1) initial flooding, (2) evaporative concentration of lake waters, (3) the movement of concentrated brine pools over the playa surface as a result of wind action, and (4) total desiccation of the lake by September 1990. During all four stages the brine chemistry of the lake was monitored. Water inflow into the Chott el Djerid basin was found to have a consistent Ca-SO₄-Cl-rich and HCO₃-CO₃-poor chemistry, reflecting the recycling of homogeneous assemblages of Cretaceous, Mio—Pliocene and Quaternary evaporites within the catchment. As the ephemeral lake shrank, these waters produced an Na-Mg-K-Cl-SO₄ brine which was similar to modern sea water. Mineral saturation data show that, during the desiccation of the lake, saturation with respect to both gypsum and halite was achieved and that the most concentrated brines were ultimately saturated with respect to potash phases. After the desiccation of the lake the main mineral phases found on the Chott included gypsum and halite. In addition, ephemeral deposits of carnallite (observed as carnallitite,3KMgCl_3·6H₂0 + NaCl) were found. This assemblage is that which would be expected to form if the waters had undergone salt norm evaporation at 1 bar pressure at 25°C (SNORM) in the evaporation model proposed by Jones and Bodine (1987). The nature of both the brine chemistry and evaporite mineralogy provides a new and rare example of marine-like potash-bearing evaporites being formed in a contemporary continental playa.     

内陆盐湖石盐流体包裹体均一温度指示意义的现代过程研究

Halite precipitation with water and air temperature was observed in detail,and homogenization temperature of fluid inclusions in halite formed in ancient and modem Chaka Salt Lake was studied.Halite precipitates mainly in August every year and largely precipitates between 13 and 15pm at one day when water temperatures reach 20℃but can seldom reach 30℃.Homogenization temperatures of fluid inclusions in halite formed in Chaka Salt Lake range from 14℃to 38℃with an average of 23.7℃.The number of inclusions appears an obvious peak value at homogenization temperatures between 18～25℃,which probably represent the water temperature in which halite mainly precipitates when water temperatures reach 20℃.Therefore,homogenization temperatures of fluid inclusions in halite formed in Chaka Salt Lake can well reflect the water temperature.     

Choosing the best ancient analogue for projected future temperatures: A case using data from fluid inclusions of middle-late Eocene halites

After the Paleocene–Eocene Thermal Maximum (PETM), global temperature and CO₂ levels decreased concurrently in the middle-late Eocene. Using different approaches, estimated CO₂ levels of the middle-late Eocene are very similar to the 1000 ppm CO₂ level projected for the next 100 years. As a result of increasing greenhouse gas concentrations, the average global temperature is projected to increase from 1.4 to 5.8 °C by 2100 relative to 2001 levels. Thus, the middle-late Eocene may be the best ancient analogue for a future with increased temperatures due to burning of fossil fuels.In order to explore the sensitivity range of global annual temperature with respect to CO₂ concentration, exact atmospheric CO₂ concentrations and air temperatures of ancient analogs must be known. Previous palynological studies provide only indirect estimates of temperature; however, the homogenization temperature of fluid inclusions in halites, obtained by the ‘cooling nucleation’ method, can provide the exact temperature of saline lake water, which is similar to overlying air temperature in shallow lakes. In this paper, we measured the range of homogenization temperatures (from 5.8 to 43.3 °C) of fluid inclusions in middle-late Eocene halites of the Yunying depression, central China. The maximum homogenization temperature of fluid inclusions (Th_max) in these middle-late Eocene halites is 4.6 °C higher than the modern extreme highest temperature (38.7 °C) recorded for this area.     

Fluid inclusions in Scourian granulites from the Lewisian complex of NW Scotland: evidence for CO2-rich fluid in Late Archaean high-grade metamorphism

In this paper the first fluid-inclusion data are presented from Late Archaean Scourian granulites of the Lewisian complex of mainland northwest Scotland. Pure CO₂ or CO₂-dominated fluid inclusions are moderately abundant in pristine granulites. These inclusions show homogenization temperatures ranging from − 54 to + 10 °C with a very prominent histogram peak at − 16 to − 32 °C. Isochores corresponding to this main histogram peak agree with P-T estimates for granulite-facies recrystallization during the Badcallian (750–800 °C, 7–8 kbar) as well as with Inverian P-T conditions (550–600 °C, 5 kbar). The maximum densities encountered could correspond to fluids trapped during an early, higher P-T phase of the Badcallian metamorphism (900–1000 °C, 11–12 kbar). Homogenization temperatures substantially higher than the main histogram peak may represent Laxfordian reworking (≤ 500 °C, < 4 kbar). In the pristine granulites, aqueous fluid inclusions are of very subordinate importance and occur only along late secondary healed fractures. In rocks which have been retrograded to amphibolite facies from Inverian and/or Laxfordian shear zones, CO₂ inclusions are conspicuously absent; only secondary aqueous inclusions are present, presumably related to post-granulite hydration processes. These data illustrate the importance of CO₂-rich fluids for the petrogenesis of Late Archaean granulites, and demonstrate that early fluid inclusions may survive subsequent metamorphic processes as long as no new fluid is introduced into the system.     

Ediacaran seawater temperature: Evidence from inclusions of Sinian halite

Seawater temperatures throughout Earth's history have been suggested to illustrate a long-term cooling trend from nearly 70 °C at ～3500 Ma to around 20 °C at ～800 Ma. The terminal Neoproterozoic prior to the “Cambrian Explosion” is a key interval in evolutionary history, as complex multicellularity appeared with the advent of the Ediacara fauna. These organisms were likely the first that required higher levels of atmospheric and dissolved marine oxygen for their sustainability. It is known that most modern macroinvertebrates are intolerant of temperatures in excess of 45 °C. Perhaps more importantly, these high seawater temperatures limit the potential of dissolved oxygen, and therefore become an integral part of this evolutionary story. Previously, our understanding of seawater temperature during the terminal Neoproterozoic comes only from ¹⁸O/¹⁶O and ³⁰Si/²⁸Si ratios ascertained from a limited number of cherts. Isotopic ratio methods for assessing seawater temperatures are inherently indirect and have a wide range of oscillation. However, maximum homogenization temperatures (Th_max) of primary fluid inclusions in halite provide a direct means of assessing brine temperature, and have been shown to correlate well with average maximum air temperatures. The oldest halites date to the Neoproterozoic–lower Paleozoic (～700–500 Ma), and Ediacaran representatives can be found in Sichuan Province, China, which do preserve primary fluid inclusions for analysis via cooling nucleation methods. We utilized halite samples from the Changning-2 well, correlative to the Dengying Formation (551–542 Ma), to provide a direct assessment of terminal Neoproterozoic seawater temperature. Our measurements indicate that seawater temperatures where these halites formed are highly similar to tropical Phanerozoic seawater temperature estimates. From compiled paleotemperature data, the decline in seawater temperatures over the course of the Proterozoic, accompanied by the reduction of seawater salinity with the sequestration of salt in massive halite deposits in the Neoproterozoic, allowed the ocean system to accumulate more dissolved oxygen, and potentially paved the way for the evolutionary innovation of complex multicellularity.     

Primary Ore Mineral Assemblage and Fluid Inclusion Study of the Batu Hijau Porphyry Cu-Au Deposit, Sumbawa, Indonesia

Abstract. The Batu Hijau porphyry Cu‐Au deposit, Sumbawa Island, Indonesia, is associated with a tonalitic intrusive complex. The temperature‐pressure condition of mineralization at the Batu Hijau deposit is discussed on the basis of fluid inclusion microthermometry. Then, the initial Cu‐Fe sulfide mineral assemblage is discussed. Bornite and chalcopyrite are major copper ore minerals associated with quartz veinlets. The quartz veinlets have been classified into ‘A’ veinlets associated with bornite, digenite, chalcocite and chalcopyrite, ‘B’ veinlets having chalcopyrite bornite along vuggy center‐line, rare ‘C’ chalcopyrite‐quartz veinlets, and late ‘D’ veinlets consisting of massive pyrite and quartz (Clode et al., 1999). Copper and gold mineralization is associated with abundant ‘A’ quartz veinlets. Abundant fluid inclusions are found in veinlet quartz consisting mainly of gas‐rich inclusions and polyphase inclusions throughout the veinlet types. The hydrothermal activity occurred in temperature‐pressure conditions of aqueous fluid immiscibility into hypersaline brine and dilute vapor. The halite dissolution (Tm[halite]) and liquid‐vapor homogenization (Th) temperatures of the polyphase inclusions in veinlet quartz range from 270 to 472d?C and from 280 to 454d?C, respectively. The estimated salinity ranges from 36 to 47 wt% (NaCl equiv.). The apparent pressures lower than 300 bars are estimated to have been along the liquid‐vapor‐halite curve for the fluid inclusions having the Th lower than the Tm that trapped the brine saturated with halite, or at slightly higher pressure relative to liquid‐vapor‐halite curve for the fluid inclusions having the Th higher than the Tm that trapped the brine unsaturated with halite. The actual temperature and pressure during the hydrothermal activity at the Batu Hijau deposit are estimated to have been around 300d?C and 50 bars. At such temperature‐pressure conditions, the principal and initial Cu‐Fe sulfide mineral assemblages are thought to be chalcopyrite + bornite solid solution (bnss) for the chalcopyrite‐bearing assemblage, and chalcocite‐digenite solid solution and bnss for the chalcopyrite‐free assemblage.     

实验室合成石盐包裹体的均一温度以及古气候意义

石盐是表生环境下形成蒸发岩系的主要矿物,在形成过程中捕获大量的原生包裹体。通过低温冷冻测温技术,可以得到石盐中原生包裹体的一系列均一温度,如何正确理解这些数据是应用石盐原生包裹体恢复古气候的关键。石盐沉积可以发生在气水界面以及水体底部,其均一温度记录了卤水结晶的温度。Lowenstein et al. (1998) 曾经用水浴法在恒定水温下合成了人工合成石盐,进行原生包裹体的均一温度研究,然而如何用水温来恢复古气温是古环境解释的关键。本次实验通过40℃下(气温,烘箱中蒸发)人工合成石盐,在岩相学观察基础上,对形成于气水界面漏斗晶中的包裹体和在底水沉积人字晶中的包裹体的均一温度进行低温冷冻测温法测定。测温过程中石盐包裹体可以得到一系列均一温度(10.6~39.9℃),而只有最大均一温度才能反映卤水结晶时的温度,两种类型的包裹体也显示了相似的最大均一温度。因此在浅水环境下,两种包裹体都可以用来反映古气温。     

四川盆地三叠纪古盐湖已达钾石盐析出阶段——来自石盐流体包裹体化学组成的约束

石盐的流体包裹体成分可提供古流体组成的物理化学信息,用以探查卤水组成变化及环境演化规律等。四川盆地位于上扬子地台,其中的早-中三叠纪沉积建造是中国海相找钾的有利层位之一。获取石盐沉积时期的卤水成分信息,是深刻认识四川盆地古海水蒸发浓缩程度的重要途径。文章利用激光剥蚀电感耦合等离子体质谱法,对采自川东地区长平3井嘉陵江组的石盐流体包裹体开展了化学组成分析,结果显示古卤水化学类型为Mg_SO4型;流体包裹体中的ρ(K~+)与现代海水浓缩到钾石盐析出阶段的ρ(K~+)基本一致,可能揭示了盆地三叠纪时期古卤水已达到钾石盐析出阶段,对四川盆地沉积环境演化及钾盐成矿规律研究等具有重要的理论意义。     

Evolution of Hydrothermal System at the Dizon Porphyry Cu-Au Deposit, Zambales, Philippines

Abstract. Evolution of hydrothermal system from initial porphyry Cu mineralization to overlapping epithermal system at the Dizon porphyry Cu‐Au deposit in western central Luzon, Zambales, Philippines, is documented in terms of mineral paragen‐esis, fluid inclusion petrography and microthermometry, and sulfur isotope systematics. The paragenetic stages throughout the deposit are summarized as follows; 1) stockwork amethystic quartz veinlets associated with chalcopyrite, bornite, magnetite and Au enveloped by chlorite alteration overprinting biotite alteration, 2) stockwork quartz veinlets with chalcopyrite and pyrite associated with Au and chalcopyrite and pyrite stringers in sericite alteration, 3) stringer quartz veinlets associated with molybdenite in sericite alteration, and 4) WNW‐trending quartz veins associated with sphalerite and galena at deeper part, while enargite and stibnite at shallower levels associated with advanced argillic alteration. Chalcopyrite and bornite associated with magnetite in quartz veinlet stockwork (stage 1) have precipitated initially as intermediate solid solution (iss) and bornite solid solution (bnss), respectively. Fluid inclusions in the stockwork veinlet quartz consist of gas‐rich inclusions and polyphase inclusions. Halite in polyphase inclusions dissolves at temperatures ranging from 360d?C to >500d?C but liquid (brine) and gas (vapor) do not homogenize at <500d?C. The maximum pressure and minimum temperature during the deposition of iss and bnss with stockwork quartz veinlets are estimated to be 460 bars and 500d?C. Fluid inclusions in veinlet stockwork quartz enveloped in sericite alteration (stage 2) consist mainly of gas‐rich inclusions and polyphase inclusions. In addition to the possible presence of saturated NaCl crystals at the time of entrapment of fluid inclusions that exhibit the liquid‐vapor homogenization temperatures lower than the halite dissolution temperatures in some samples, wide range of temperatures of halite dissolution and liquid‐vapor homogenization of polyphase inclusions from 230d?C to >500d?C and from 270d?C to >500d?C, respectively, suggests heterogeneous entrapment of gaseous vapor and hypersaline brine. The minimum pressure and temperature are estimated to be about 25 bars and 245d?C. Fluid inclusions in veinlet quartz associated with molybdenite (stage 3) are dominated by gas‐rich inclusions accompanied with minor liquid‐rich inclusions that homogenize at temperatures between 350d?C and 490d?C. Fluid inclusions in vuggy veinlet quartz associated with stibnite (stage 4) consist mainly of gas‐rich inclusions with subordinate polyphase inclusions that do not homogenize below 500d?C. Fluid inclusions in veinlet quartz associated with galena and sphalerite (stage 4) are composed of liquid‐rich two‐phase inclusions, and they homogenize into liquid phase at temperatures ranging widely from 190d?C to 300d?C (suggesting boiling) and the salinity ranges from 1.0 wt% to 3.4 wt% NaCl equivalent. A pressure of about 15 bars is estimated for the dilute aqueous solution of 190d?C from which veinlet quartz associated with galena and sphalerite precipitated. In addition to a change in temperature‐pressure regime from lithostatic pressure during the deposition of iss and bnss with stockwork quartz veinlets to hydrostatic pressure during fracture‐controlled quartz veinlet associated with galena and sphalerite, a decrease in pressure is supposed to have occurred due to unroofing or removal of the overlying piles during the temperature decrease in the evolution of hydrothermal system. The majority of the sulfur isotopic composition of sulfides ranges from ±0 % to +5 %. Sulfur originated from an iso‐topically uniform and homogeneous source, and the mineralization occurred in a single hydrothermal system.     

察尔汗盐湖石盐的流质包裹体氢氧稳定同位素分析及其地球化学意义

本文是在建立了盐酸胍法制备样品用于氧同位素分析方法研究的基础上,测定了察尔汗湖区各类天然水及ZK88-01占孔岩心的原生石盐流质包裹体氢氧稳定同位素组成。该方法适用于高盐度卤水微量δ18O分析,具有成本低、操作简便和定量转化的优点,值得在国内推广。 根据原生石盐包体水δD、δ18O的分布特征,论述了察尔汗盐湖距今5万年来湖水的演化历程。划分出三种不同成盐环境下的演化期,各期中古湖水体具有波动的继承性,各期间可能存在成盐环境的突变.根据天然水δD、δ18O关系初步获得该区蒸发线为:δD=2.5δ18O-45.3;证实了剖面上部淤泥水与达布逊湖水下渗有关;下部明显地有侧向水补给.     

Geochemistry of saline minerals separated from Lake Qarun brine

Lake Qarun is an inland saline lake of the type Na---(Mg)---Cl---(SO₄). The SO₄/Cl weight ratio exceeds 0.6. The sequence of salt deposition, upon mechanical evaporation at 70°C, starts with basanite and halite, passes with magnesium sulphate minerals and ends with sylvite and carnallite. High concentrations of Sr in the gypsiferous fraction and B in the end-residue are recorded.     

大兴安岭岔路口斑岩钼矿床流体成分及成矿意义

岔路口超大型斑岩型钼矿床位于大兴安岭北段,以网脉状和角砾岩型矿化为主.该矿床经历了4个成矿阶段:Ⅰ.石英-钾长石;Ⅱ.石英-辉钼矿;Ⅲ.石英-多金属硫化物;Ⅳ.石英-萤石-方解石.包裹体的岩相学及激光拉曼研究揭示,石英斑晶内的熔体-流体包裹体中熔体成分有更长石和钠长石,为岩浆出溶作用形成;子矿物多相包裹体(S型)中含有钾盐、石盐、赤铁矿和石膏等子矿物,显示出成矿流体为高氧逸度.第Ⅰ成矿阶段包裹体有气液两相(L+V型)、富CO₂三相(C型)和含石盐、钾盐、赤铁矿及硬石膏等子矿物的多相(S型)等类型,第Ⅱ成矿阶段除了有L+V型、C型以及含钾盐、石盐、黄铜矿和辉钼矿等子矿物多相(S型)外,还可以见到S型包裹体与气相包裹体(V型)共存;第Ⅲ成矿阶段以L+V型和含方解石的S型包裹体为主;第Ⅳ成矿阶段除见到L+V型包裹体外,还可以见到液相包裹体(L型).显微测温结果显示从早到晚,流体包裹体均一温度从530 ℃变为120 ℃、盐度从66.7% NaCl equiv变为1.2% NaCl equiv,呈现逐渐降低的趋势.群体包裹体成分显示各阶段均含有气相CO₂,液相成分中Na+,K+,Ca2+,SO₄2-,Cl-含量很高,而F-含量极少.成矿流体总体属于富含CO₂的高盐度、高氧逸度的NaCl-H₂O-CO₂体系,在流体演化过程中温度、氧逸度、盐度和CO₂含量逐渐降低.温度、盐度、CO₂含量逐渐降低及绢云母化影响了矿石沉淀.      

Copper mineralization around the Ahar batholith, north of Ahar (NW Iran): Evidence for fluid evolution and the origin of the skarn ore deposit

This investigation presents and interprets fluid inclusion data from different lithological units of the Cu skarn deposits at Mazraeh, north of Ahar, Azarbaijan, NW Iran. The results provide an assessment of the P–T conditions and mineral–fluid evolution and suggest new exploration parameters. Five types of inclusions are recognized from quartz and garnet. The temperature of homogenization of Type I inclusions with daughter minerals halite and sylvite ranges from 312° to 470 °C with total salinity of 52 to 63 wt.% NaCl equiv.; Type II and III inclusions with halite have homogenization temperatures of 230° to 520 °C and salinity of 31 to 50 wt.% NaCl equiv. The salinity of Types IV and V biphase (liquid + vapor) inclusions, based on their final ice melting temperature, varies between 10.2 to 20.8 wt.% NaCl equiv. T_h vs. salinity plots of inclusions show that the salinity of the fluids correlates positively with temperature. The inclusions formed at low pressure. Changes in the temperature and salinity of the fluids can be reconstructed from the inclusions. Highly saline, high-temperature fluids were most abundant during the main chalcopyrite ore-forming phase in the skarn and mineralized quartz veins. Low-salinity aqueous fluids were abundant in barren veins, in which there is no evidence for early hot high-salinity brine, and might have resulted from late-stage dilution and mixing of hydrothermal fluids with meteoric water. Based on petrographic features and fluid-inclusion data, early-stage magnetite deposition is related to boiling of fluid at temperatures of about 500 °C. At a later stage, boiling at temperatures of around 320° to 400 °C favored the deposition of sulfides and Fe mobility was decreased at these lower temperatures. The following inclusion characteristics may be used as exploration parameters in the Mazraeh area. (i) Presence of high-temperature, salt-bearing inclusions, with T_h between 300 and 500 °C; (ii) High-salinity fluid inclusions; and (iii) Inclusions showing evidence of boiling of the fluid. In addition, the presence of magnetite is an important exploration parameter.     

Abiogenic Fischer–Tropsch synthesis of hydrocarbons in alkaline igneous rocks; fluid inclusion, textural and isotopic evidence from the Lovozero complex, N.W. Russia

A detailed fluid inclusion study has been carried out on the hydrocarbon-bearing fluids found in the peralkaline complex, Lovozero. Petrographic, microthermometric, laser Raman and bulk gas data are presented and discussed in context with previously published data from Lovozero and similar hydrocarbon-bearing alkaline complexes in order to further understand the processes which have generated these hydrocarbons. CH₄-dominated inclusions have been identified in all Lovozero samples. They occur predominantly as secondary inclusions trapped along cleavage planes and healed fractures together with rare H₂O-dominant inclusions. They are consistently observed in close association with either arfvedsonite crystals, partially replaced by aegirine, aegirine crystals or areas of zeolitization. The majority of inclusions consist of a low-density fluid with CH₄ homogenisation temperatures between −25 and −120 °C. Those in near-surface hand specimens contain CH₄+H₂ (up to 40 mol%)±higher hydrocarbons. However, inclusions in borehole samples contain CH₄+higher hydrocarbons±H₂ indicating that, at depth, higher hydrocarbons are more likely to form. Estimated entrapment temperatures and pressures for these inclusions are 350 °C and 0.2–0.7 kbar. A population of high-density, liquid, CH₄-dominant inclusions have also been recorded, mainly in the borehole samples, homogenising between −78 and −99 °C. These consist of pure CH₄, trapped between 1.2 and 2.1 kbar and may represent an early CH₄-bearing fluid overprinted by the low-density population. The microthermometric and laser Raman data are in agreement with bulk gas data, which have recorded significant concentrations of H₂ and higher hydrocarbons up to C₆H₁₂ in these samples. These data, combined with published isotopic data for the gases CH₄, C₂H₆, H₂, He and Ar indicate that these hydrocarbons have an abiogenic, crustal origin and were generated during postmagmatic, low temperature, alteration reactions of the mineral assemblage. This would suggest that these data favour a model for formation of hydrocarbons through Fischer–Tropsch type reactions involving an early CO₂-rich fluid and H₂ derived from alteration reactions. This is in contrast to the late-magmatic model suggested for the formation of hydrocarbons in the similar peralkaline intrusion, Ilímaussaq, at temperatures between 400 and 500 °C.     

Implications of super dense carbonic and hypersaline fluid inclusions in granites from the Ranchi area, Chottanagpur Gneissic Complex, Eastern India

A combined fluid inclusion and mineral thermobarometric study in groups of synchronous inclusions in quartz within weakly foliated granites from the Chottanagpur Gneissic Complex, India, reveals super dense carbonic (CO₂ with minor CH₄ and H₂O) inclusions and hypersaline (H₂O–NaCl ± NaHCO₃) inclusions, with halite- and nahcolite daughter phases. This study documents the highest density (1.115 g cm^− 3) CO₂ fluids ever reported in granites. Fluid isochores, constructed from CO₂ (± CH₄) and halite-bearing inclusions, coupled with two-feldspar thermometry constrain the minimum P–T at 8 kbar/ 750 °C for fluid entrapment in granites. By contrast, the carbonic inclusions in quartz from granite-hosted metapelite enclaves contain substantial CH₄ (up to 30 mol%), and the entrapment pressure ( 4.3 kbar/600 °C) is considerably lower compared to those in the granites. By implication, the sillimanite-free granites were not derived from the metapelitic enclaves, and instead were formed by partial melting of fluid-heterogeneous lower crustal protoliths, with fluid entrapment at magmatic conditions.