Growth of Emerald Crystals by Evaporation of Na2O—MoO3 Flux

Well-formed crystals of emerald, Be3AI2Si6O18:Cr, were easily grown from an Na2O-MoO3 flux by an isothermal technique. The crystal growth was conducted by heating a mixture of solute and flux at 1 100 ℃ for 24 h. The evaporation loss of flux depended on the amount of Na2O added to MoO3. Emerald crystals of lengths up to 2.1 mm and widths of 1. 4 mm were grown. The crystal sizes were dependent on the evaporation loss of the flux. The obtained crystals were transparent and exhibited the typical emerald-green color. The form of the emerald crystals was a twelve-sided prism bounded by well-developed faces. The aspect ratios were in the region of 1. 4 to 2. 3. The density was (2. 64±0.02) g/cm3. The IR absorption bands were in good agreement with the literature data.     

Removal of Cu（ Ⅱ） from Wastewater Using Acidified Sewage Sludge Ash

Sewage sludge ash (SSA), the waste generated in sewage sludge incineration, was obtained from Wuhan Sewage Treatment Plant and used as a low-cost sorbent for removing Cu (Ⅱ) from wastewaters. The sorbent was first modified with 5 % sulfuric acid to increase its sorption capacity. The specific surface area, porosity, cation-exchange capacity (CEC) and pHzzc of the sorbent were measured. Batch experiments were made to study the effect of contact time, solution pH value and temperature on sorption. Both Langmuir and Freundlich models well described the Cu (Ⅱ) sorption process,with correlation coefficient (R2 ) values of 0. 993 4 and 0.9899 respectively. And the sorption process follows the Lagergren first order kinetic model. The equilibrium sorption capacity of acidified SSA to Cu(Ⅱ) is estimated to be 7.78 mg/g under optimal conditions.     

Migration Fractionation of Neutral Nitrogen Compounds of Crude Oils from Tabei Oilfield in the Tarim Basin, China

The absolute amounts and relative distributions of neutral nitrogen compounds in the Tabei oilfield (e. G. Blocks Ln1-Ln1 1) showed remarkable migration fractionation in the vertical direction. From Ordovician reservoirs (O) to oil legs TⅢ and T Ⅰ of Triassic reservoirs in blocks LN1-LN11, the concentrations of [a] [c] decreased from 1. 59μg/g, 0.49μg/g to 0.17 μg/g (oil). The ratios of various alkylcarbazole isomers, such as 1,8-dimethylcarbazole/nitrogenpartially shielded isomers and 1,8-dimethylcarbazole/nitrogen-exposed isomers, were adopted as the indicators of petroleum migration. The ratios increased from 0.13, 0.20 to 0.67 and from going from the south to the north of the Tabei oilfield, the absolute concentrations of neutral nitrogen compounds decreased drastically, and the nitrogen-shielded isomers were enriched relative to nitrogen-exposed isomers and nitrogen-partially shielded isomers. Crude oils in the Tabei oilfield migrated laterally from the Jilake structure to the Sangtamu fault uplift and Lunnan fault uplift, and crude oils in the same fault uplift migrated and remigrated vertically from Ordovician reservoirs, to oil legs TⅢ to TⅠ of Triassic reservoirs.     

A novel strategy using biodegradable EDDS for the chemically enhanced phytoextraction of soils contaminated with heavy metals

For the sake of cost and potential environmental risk, it is necessary to minimize the amount of chelates used in chemically-enhanced phytoextraction. In the present study, a biodegradable chelating agent, EDDS was added in a hot solution at 90℃ to the soil in which garland chrysanthemum （Chrysanthemum coronarium L.） and beans （Phaseolus vulgaris L., white bean） were growing. The application of hot chelate solutions was much more efficient than the application of normal chelate solutions （25℃） in improving the uptake of heavy metals by plants. When 1 mmol kg1 of EDDS as a hot solution was applied to soil, the concentrations ofCu, Zn and Cd and the total phytoextraction by the shoots of the two plant species exceeded or approximated those in the shoots of plants treated with 5 mmol kg^-1 of normal EDTA solution. The concentrations of metals in the shoots of beans were significantly correlated with the relative electrolyte leakage rate of root cells, indicating that the root damage resulting from the hot solution might play an important role in the process of chelate-enhanced metal uptake. The soil leaching study demonstrated that decreasing the dosage of chelate resulted in decreased concentrations of soluble metals in soils. On the 28th day following the application of chelate, the concentrations of soluble metals in the EDDS treated soil were not significantly different from the concentrations in the control soil to which chelates had not been applied.     

Ultrahigh-pressure and Retrograde Metamorphic Ages for Paleozoic Protolith of Paragneiss in the Main Drill Hole of the Chinese Continental Scientific Drilling Project （CCSD-MH）, SW Sulu UHP Terrane

Laser Raman spectroscopy and cathodoluminescence (CL) images show that most zircon crystals separated from paragneiss in the main drill hole of the Chinese Continental Scientific Drilling Project (CCSD-MH) at Maobei, southwestern Sulu terrane, contain low-pressure mineral-bearing detrital cores, coesite-bearing mantles and quartz-bearing or mineral inclusion-free rims. SHRIMP U Pb dating on these zoned zircons yield three discrete and meaningful age groups. The detrital cores yield a large age span from 659 to 313 Ma, indicating the protolith age for the analyzed paragneiss is Paleozoic rather than Proterozoic. The coesite-bearing mantles yield a weighted mean age of 228 ± 5 Ma for the UHP event. The quartz-bearing outmost rims yield a weighted mean age of 213 ± 6 Ma for the retrogressive event related to the regional amphibolite facies metamorphism in the Sulu UHP terrane. Combined with previous SHRIMP U-Pb dating results from orthogneiss in CCSD-MH, it is suggested that both Neoproterozoic granitic protolith and Paleozoic sedimentary rocks were subducted to mantle depths in the Late Triassic. About 15 million years later, the Sulu UHP metamorphic rocks were exhumed to mid-crustal levels and overprinted by an amphibolite-facies retrogressive metamorphism. The exhumation rate deduced from the SHRIMP data and metamorphic P-T conditions is about 6.7 km/Ma. Such a fast exhumation suggests that the Sulu UHP paragneiss and orthogneiss returned towards the surface as a dominant part of a buoyant sliver, caused as a consequence of slab breakoff.     

Isotopic composition of dissolved boron and its geochemical behavior in a freshwater-seawater mixture at the estuary of the Changjiang （Yangtze） River

The isotopic composition of dissolved boron, in combination with the elemental concentrations of B, Cl and salinities in freshwater-seawater mixed samples taken from the estuary of the Changjiang River, the largest one in China, was investigated in detail in this study. Brackish water and seawater samples from the estuary of the Changjiang River were collected during low water season in November, 1998. Boron isotopic compositions were determined by the Cs2BO^＋2-graphite technique with a analytical uncertainty of 0.2‰ for NIST SRM 951 and an average analytical uncertainty of 0.8‰ for the samples. The isotopic compositions of boron, expressed in δ^11B, and boron concentrations in the Changjiang River at Nanjing and seawater from the open marine East Sea, China, are characterized by δ^11B values of -5.4‰ and 40.0‰, as well as 0.0272 and 4.43 mg B/L, respectively. Well-defined correlations between δ^11B values, B concentrations and Cl concentrations are interpreted in terms of binary mixing between fiver input water and East Sea seawater by a process of straightforward dilution. The offsets of δ^11B values are not related to the contents of clastic sediment and to the addition of boron. These relationships favor a conservative behavior of boron at the estuarine of the Changjiang River.     

Helium and argon isotopic compositions of the Longquanzhan gold deposit in the Yishu fault zone and their geological implications

The Longquanzhan gold deposit hosted in granitic cataclasites with mylontization of the foot wall of the main Yishui-Tangtou fault. 3He/4He ratios in fluid inclusions range from 0. 14 to 0. 24 R/Ra,close to those of the crust-source helium. 40Ar/36Ar ratios were measured to be 289-1811, slightly higher than those of atmospheric argon. The results of analysis of helium and argon isotopes suggested that ore-forming fluids were derived chiefly from the crust. The δ18O values of fluid inclusions from vein quartz range from -1.78‰ to 4.07‰, and the δD values of the fluid inclusions vary between -74‰ and -77‰. The hydrogen and oxygen isotope data indicated that the ore-forming fluid for the Longquanzhan gold deposit had mixed with meteoric water in the process of mineralization. This is consistent with the conclusion from the helium and argon isotope data.     

Seasonal distribution of total mercury and methylmercury in sediments of the Wujiangdu Reservoir, Guizhou, China

The concentrations of total mercury and methylmercury in sediments were determined at the dam of the Wujiangdu Reservoir in different seasons. Total mercury (HgT) levels in the whole sediment profile were 254.2±47.0 ng/g in winter, 254.2±31.6 ng/g in spring, and 256.7±60.8 ng/g in summer, without significant variations in different seasons or at different depths. In contrast, the methylmercury (MeHg) compounds were most abundant at the sediment-water interface and decreased progressively with depth. MeHg contents of the sediments during different seasons are highly dependent on microbial activity, and seem to be higher when Hg (II)-methylating microorganisms are active. Thus, MeHg levels tend to rise in the loci where nutrient supplies and biological productivity are favorable. The percentage of HgT that is present as MeHg in the sediments increased gradually from December 2003 to April 2004 and to July 2004.     

Extension of the Louzidian Metamorphic Core Complex and Development of Supradetachment Basins in Southern Chifeng, Inner Mongolia, China

The Louzidian metamorphic core complex (LMCC) in southern Chifeng is located on the northern margin of the North China craton. Structural analyses of the LMCC and its extensional detachment system indicate that the LMCC experienced two-stage extension. The ductile regime experienced top-to-northeast shearing extension and the brittle detachment fault underwent top-down-outwards slipping. Between these two stages, a semi-ductile regime recorded the transition from ductile to brittle. The hanging wall of the detachment fault is similar to those classic supradetachment basins in western North America. Analyses of provenance and paleocurrent directions in the basins show that there were two filling stages. In the early stage, materials came from the southwest margin of the basin and the hanging wall of the detachment system and were transported from southwest to northeast; while in the late stage, deposits were derived from the footwall of the detachment fault and transported outwards to the two sides of the     

Permafrost and taliks and their changes on the south and north banks of the Tuotuo River in the Qinghai-Tibet Plateau under the climate warming北大核心CSCD

The distribution of permafrost and taliks is very complex in the Tuotuo River Basin(TRB), which is located in interior of the Qinghai-Tibet Plateau. Characterizing the spatial distribution and the thermal stability of permafrost and taliks is of great significance to community activities and engineering construction in TRB. Based on the zonation of permafrost and talik distribution around TRB conducted in the 1980s, the soil temperature and its variation process of permafrost and taliks in the south and north banks of the Tuotuo River were analyzed by using the observation data of five boreholes(N1~N5)along the Qinghai-Tibet Railway in the north bank and five boreholes(S1~S5)on the first terrace in the south bank. The results showed that, under the climate warming, permafrost and taliks in the north banks experienced significant degradation and warming process. From 2005 to 2020, the permafrost at the N1 borehole has undergone a significant down-draw degradation process, from extremely unstable and high-temperature permafrost to thawed zone. From 2005 to 2013, the annual average ground temperature of the talik at N2 increased at a rate of 0. 3~0. 4 °C·(10a)-1. At Maqutang on the south bank, permafrost prevails from the first-class terrace to the gentle slope of the Kaixinling Mountain, with both through and non-through taliks on the first-class terrace. The spatial distribution and the thermal stability of permafrost and talik in the TRB are further promoted by analyzing the changes in temperatures at boreholes in the basin. However, to meet the requirements of mapping and engineering construction of permafrost and taliks in the TRB, it is still necessary to carry out geological investigation with multiple methods and in-depth research on development mechanism of taliks in the future. © 2022 Nanjing Forestry University. All rights reserved.     

Causes of variation in crystal morphology in metamorphogenic pyrite deposits of the Cameros Basin (N Spain)

The low‐grade metasediments of the Cameros Basin, northern Spain, host a number of deposits of spectacular quality pyrite mineralization. These formed during regional metamorphism and the pyrite crystals exhibit a wide range of morphologies. On the basis of pyrite crystal habit, the deposits can be classified into two groups: Group I comprises deposits with cubic, elongated or platy crystals; Group II comprises deposits characterized by pyritohedra and cubo‐pyritohedra with striated faces, along with blocky crystals and fine‐grained aggregates. Group I deposits are formed in sequences dominated by meandriform fluviatile sediments, while Group II is hosted by deltaic plain and lacustrine metasediments. Temperature differences between deposits and As content are possible causes of the different pyrite morphologies in the deposits, but no significant variation exists between the two groups for either factor. Comparison with experimentally grown pyrite crystals suggests that Group I deposits have morphologies indicative of lower degrees of pyrite supersaturation than pyrite crystals in Group II deposits. The sedimentary facies hosting Group II deposits provides a greater availability of sedimentary sulphur (pyrite and sulphates). Moreover, reactions involving sulphate during metamorphism may have modified fluid chemistry, which would also act to produce higher degrees of pyrite saturation in fluids derived from the sulphate‐rich deltaic plain and lacustrine metasediments hosting the Group II deposits. This hypothesis is confirmed by sulphur isotope data on the pyrites, which show a larger component of³⁴S‐enriched sulphate‐derived sulphur in these deposits. Copyright © 2001 John Wiley & Sons, Ltd.     

Magma hybridization in the Western Tatra Mts. granitoid intrusion (S-Poland, Western Carpathians)

In the Variscan Western Tatra granites hybridization phenomena such as mixing and mingling can be observed at the contact of mafic precursors of dioritic composition and more felsic granitic host rocks. The textural evidence of hybridization include: plagioclase?CK-feldspar?Csphene ocelli, hornblende- and biotite-rimmed quartz ocelli, plagioclase with Ca-rich spike zonation, inversely zoned K-feldspar crystals, mafic clots, poikilitic plagioclase and quartz crystals, mixed apatite morphologies, zoned K-feldspar phenocrysts. The apparent pressure range of the magma hybridization event was calculated at 6.1?kbar to 4.6?kbar, while the temperature, calculated by independent methods, is in the range of 810°C?770°C. U-Pb age data of the hybrid rocks were obtained by in-situ LA-MC-ICP-MS analysis of zircon. The oscillatory zoned zircon crystals yield a concordia age of 368?±?8?Ma (MSWD?=?1.1), interpreted as the age of magma hybridization and timing of formation of the magmatic precursors. It is the oldest Variscan magmatic event in that part of the Tatra Mountains.     

Graphite morphologies from the Borrowdale deposit (NW England,UK): Raman and SIMS data

Graphite in the Borrowdale (Cumbria, UK) deposit occurs as large masses within mineralized pipe-like bodies, in late graphite–chlorite veins, and disseminated through the volcanic host rocks. This occurrence shows the greatest variety of crystalline graphite morphologies recognized to date from a single deposit. These morphologies described herein include flakes, cryptocrystalline and spherulitic aggregates, and dish-like forms. Colloform textures, displayed by many of the cryptocrystalline aggregates, are reported here for the first time from any graphite deposit worldwide. Textural relationships indicate that spherulitic aggregates and colloform graphite formed earlier than flaky crystals. This sequence of crystallization is in agreement with the precipitation of graphite from fluids with progressively decreasing supersaturation. The structural characterization carried out by means of Raman spectroscopy shows that, with the exception of colloform graphite around silicate grains and pyrite within the host rocks, all graphite morphologies display very high crystallinity. The microscale SIMS study reveals light stable carbon isotope ratios for graphite (δ ¹³C = −34.5 to −30.2‰), which are compatible with the assimilation of carbon-bearing metapelites in the Borrowdale Volcanic Group magmas. Within the main mineralized breccia pipe-like bodies, the isotopic signatures (with cryptocrystalline graphite being lighter than flaky graphite) are consistent with the composition and evolution of the mineralizing fluids inferred from fluid inclusion data which indicate a progressive loss of CO₂. Late graphite–chlorite veins contain isotopically heavier spherulitic graphite than flaky graphite. This agrees with CH₄-enriched fluids at this stage of the mineralizing event, resulting in the successive precipitation of isotopically heavier graphite morphologies. The isotopic variations of the different graphite morphologies can be attributed therefore, to changes in the speciation of carbon in the fluids coupled with concomitant changes in the XH₂O during precipitation of graphite and associated hydrous minerals (mainly epidote and chlorite).     

Supergene geochemistry and crystal morphology of gold in a semiarid weathering environment: application to gold exploration

Oxidation of sulfide- and carbonate-rich vein gold deposits under semiarid conditions can be represented as a three-stage process, each creating supergene environments conducive to dissolution and reprecipitation of gold-silver alloys. The three-stage weathering process of sulfide-carbonate gold veins is depth-dependent, and develops from the relatively young, lowermost weathering horizon just below the water table, through an intermediate weathering horizon in the oxidation zone above the water table, and culminating in the oxide-rich upper saprolite and oxisol.Neoformed gold crystals in the weathering profile have distinct composition and morphologic characteristics from the hypogene gold crystals associated with the sulfide- and carbonate-rich ores. Two distinct types of secondary gold are present in the weathering profile: (1) gold crystals associated with sulfates and arsenates; and (2) gold crystals associated with iron and aluminum oxides/hydroxides, or with kaolinite. The distinct crystal morphologies and mineralogical associations of primary and secondary gold are useful in prospecting for gold deposits in weathered terrains.     

Zn-, Mn- and Co-rich chromian spinels from the Bou-Azzer mining district (Morocco): Constraints on their relationship with the mineralizing process

The Co–Ni arsenides from the Bou-Azzer mining district contain disseminated chromian spinels with the highest Zn, Mn and Co contents ever reported up to date in any geological environment. The rationale behind this study was checking the role of Zn, Mn and Co contents in chromian spinel as possible indicators of mineralized environments. To tackle this issue the chemical compositional variations of chromian spinel disseminated in barren serpentinite, in Co arsenide ores and in Cu sulphide ores from three different deposits (Aghbar, Tamdrost and Aït-Ahmane mines) were studied focusing on the alteration patterns of chromian spinel grains, their fracturing degree and relationship with the precipitation of ore minerals. Results show that chromian spinel crystals are zoned and strongly fractured. They record, at least, two fracturation events: an early one developed before or coeval with the alteration process that gave rise to the zoning, and a second one that disrupted the zoning pattern splitting the altered grains in fragments which became included and partly dissolved in arsenide minerals. The early fracturing and alteration of chromite occurred during the Pan-African orogenesis and became fractured again during the Variscan tectono-metamorphic evolution of the Bou-Azzer ophiolite, just before the formation of arsenide ores. Maximum ZnO contents (up to 19.7 wt.%) occur in cores of chromian spinels associated with Co minerals from Aghbar, MnO reaches its maximum (21.4 wt.%) in rims of crystals included in chalcopyrite and CoO (up to 2.3 wt.%) concentrates in cores of grains hosted by skutterudite (CoAs₃), all them from Aghbar mine. Chromian spinels from Tamdrost and Aït-Ahmane ores have much lower contents in these elements. Zn and Mn concentration in chromian spinel are neither related with the ore type nor with the mineralization degree of the host suggesting that these elements became enriched in chromian spinel during its early, ocean-floor alteration in a metal-rich environment characterized by the nearby presence of hydrothermal vent fields and forming volcano-sedimentary massive sulphide deposits (e.g. the Bleida deposit). In contrast, Co cannot be upgraded up to the levels measured in these chromian spinel grains in this ocean floor environment but its high contents seem to be related with the formation of the arsenide ores.     

Morphology and microstructure of chromite crystals in chromitites from the Merensky Reef (Bushveld Complex, South Africa)

The Merensky Reef of the Bushveld Complex consists of two chromitite layers separated by coarse-grained melanorite. Microstructural analysis of the chromitite layers using electron backscatter diffraction analysis (EBSD), high-resolution X-ray microtomography and crystal size distribution analyses distinguished two populations of chromite crystals: fine-grained idiomorphic and large silicate inclusion-bearing crystals. The lower chromitite layer contains both populations, whereas the upper contains only fine idiomorphic grains. Most of the inclusion-bearing chromites have characteristic amoeboidal shapes that have been previously explained as products of sintering of pre-existing smaller idiomorphic crystals. Two possible mechanisms have been proposed for sintering of chromite crystals: (1) amalgamation of a cluster of grains with the same original crystallographic orientation; and (2) sintering of randomly orientated crystals followed by annealing into a single grain. The EBSD data show no evidence for clusters of similarly oriented grains among the idiomorphic population, nor for earlier presence of idiomorphic subgrains spatially related to inclusions, and therefore are evidence against both of the proposed sintering mechanisms. Electron backscatter diffraction analysis maps show deformation-related misorientations and curved subgrain boundaries within the large, amoeboidal crystals, and absence of such features in the fine-grained population. Microstructures observed in the lower chromitite layer are interpreted as the result of deformation during compaction of the orthocumulate layers, and constitute evidence for the formation of the amoeboid morphologies at an early stage of consolidation. An alternative model is proposed whereby silicate inclusions are incorporated during maturation and recrystallisation of initially dendritic chromite crystals, formed as a result of supercooling during emplacement of the lower chromite layer against cooler anorthosite during the magma influx that formed the Merensky Reef. The upper chromite layer formed from a subsequent magma influx, and hence lacked a mechanism to form dendritic chromite. This accounts for the difference between the two layers.     

Facies analysis of the Trypali carbonate unit (Upper Triassic) in central-western Crete (Greece): an evaporite formation transformed into solution-collapse breccias

The Trypali carbonate unit (Upper Triassic), which crops out mainly in central‐western Crete, occurs between the parautochthonous series (Plattenkalk or Talea Ori‐Ida series, e.g. metamorphic Ionian series) and the Tripolis nappe (comprising the Tripolis carbonate series and including a basal Phyllite–Quartzite unit). It consists of interbedded dolomitic layers, represented principally by algally laminated peloidal mudstones, foraminiferal, peloidal and ooidal grainstones, as well as by fine‐grained detrital carbonate layers, in which coarse baroque dolomite crystals and dolomite nodules are dispersed. Baroque dolomite is present as pseudomorphs after evaporite crystals (nodules and rosettes), which grew penecontemporaneously by displacement and/or replacement of the host sediments (sabkha diagenesis). However, portions of the evaporites show evidence of resedimentation. Pre‐existing evaporites predominantly consisted of skeletal halite crystals that formed from fragmentation of pyramidal‐shaped hoppers, as well as of anhydrite nodules and rosettes (salt crusts). All microfacies are characteristic of peritidal depositional environments, such as sabkhas, tidal flats, shallow hypersaline lagoons, tidal bars and/or tidal channels. Along most horizons, the Trypali unit is strongly brecciated. These breccias are of solution‐collapse origin, forming after the removal of evaporite beds. Evaporite‐related diagenetic fabrics show that there was extensive dissolution and replacement of pre‐existing evaporites, which resulted in solution‐collapse of the carbonate beds. Evaporite replacement fabrics, including calcitized and silicified evaporite crystals, are present in cements in the carbonate breccias. Brecciation was a multistage process; it started in the Triassic, but was most active in the Tertiary, in association with uplift and ground‐water flow (telogenetic alteration). During late diagenesis, in zones of intense evaporite leaching and brecciation, solution‐collapse breccias were transformed to rauhwackes. The Trypali carbonate breccias (Trypali unit) are lithologically and texturally similar to the Triassic solution‐collapse breccias of the Ionian zone (continental Greece). The evaporites probably represent a major diapiric injection along the base of the parautochthonous series (metamorphic Ionian series) and also along the overthrust surface separating the parautochthonous series from the Tripolis nappe (Phyllite–Quartzite and Tripolis series). The injected evaporites were subsequently transformed into solution‐collapse breccias.     

Origin of quartz cements in some sandstones from the Jurassic of the Inner Moray Firth (UK)

The extent of quartz cementation in shallow marine sandstones of the Brora Arenaceous Formation (Oxfordian) is closely related to the occurrence and abundance of Rhaxella perforata sponge spicules. Three cement morphologies are identified, chalcedonic quartz, microquartz and mesoquartz. Chalcedonic quartz forms matrix-supported cements which preserve moulds of Rhaxella spicules. Chalcedonic quartz crystals have inequant development of crystal faces, on average 0·1 μm in diameter, and are the first formed cement and reveal homogeneous dark grey tones on the SEM-CL/BEI. Microquartz forms 5–10 μm diameter crystals, which commonly grow on chalcedonic quartz substrates and show various grey tones under SEM-CL/BEI. Mesoquartz crystals grow in optical continuity with their host grains, have >20 μm a-axial diameter crystals, and exhibit distinctly zoned luminescence. Although no opaline silica is preserved, the quartz cement is interpreted to have formed from an opaline precursor. Detrital quartz has an average δ¹⁸O composition of + 12·2‰ and mesoquartz (syntaxial overgrowth) has an average δ¹⁸O composition of +20·0‰. Estimates of the δ¹⁸O compositions of microquartz and chalcedonic quartz are complicated by the problem of isolating the two textural types; mixtures of the two give consistently higher δ¹⁸O compositions than mesoquartz, the higher estimate being +39·2‰. From oxygen isotope data the formation of quartz, microquartz and chalcedonic quartz is interpreted to have taken place between 35 and 71°C in marine derived pore waters. Organic and inorganic maturation data constrain the upper temperature limit to less than 60°C.     

水热条件下黄铁矿片、板状晶体的微结构

利用透射电子显微镜(TEM)系统观测了黄铁矿片、板状晶体的微结构,发现在水热条件下生成的黄铁矿片、板状晶体具有正方形、矩形等多种形貌。其中,正方形较多,矩形次之,另可见到一些其他不规则形状。黄铁矿片、板状晶生长完好,未见缺陷。经测定多数四边形片状黄铁矿的两组边分别平行(010)和(100),其生长晶面为(001);个别四边形片状黄铁矿的两组边分别平行(010)和(101),其生长晶面为(101),矩形片状黄铁矿长轴生长方向为001。在水热条件下黄铁矿以多形貌出现,黄铁矿的片、板状晶体多数是沿(001)面生长的结果,(001)为黄铁矿片、板状晶体的主要二维生长面,并沿001方向扩展,构成了二维晶体。