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1.
Al_2O_3和Ti在风化和热液蚀变等地球化学过程中通常被认为是不活动元素,两者的比值Al_2O_3/Ti常被用来指示地球化学作用过程。通过对中国157件火成岩样品元素含量平均值的统计发现,火成岩样品中Al_2O_3/Ti与SiO_2含量值之间存在着较好的幂函数关系:ln(Al_2O_3/Ti)=0.073×SiO_2-0.89,式中Al_2O_3和SiO_2和Ti含量单位均为%。本文基于得到的经验方程和TAS图解构建了一个新的判别岩石类型的图解——Al_2O_3-Ti图解。该图解可以区分酸性岩、中酸性岩、中性岩、中基性岩-基性岩四类岩性。通过对三个火成岩风化剖面的研究发现,花岗岩风化剖面从新鲜基岩到风化形成的土壤在Al_2O_3-Ti图解中均落在酸性岩区,花岗闪长岩风化剖面从新鲜基岩到风化形成的土壤样品均落在中酸性岩区,玄武质安山岩风化剖面从新鲜基岩到风化形成的土壤样品均落在中基性岩-基性岩区。不同风化程度的风化产物与其母岩在Al_2O_3-Ti图解中所在的区域一致,即Al_2O_3-Ti图解可以用来追溯火成岩风化产物的母岩岩性。通过对胶东焦家金矿和豫西牛头沟金矿两个矿区岩石的研究发现,黑云母花岗岩从新鲜岩石到其蚀变岩及其形成矿石的样品在Al_2O_3-Ti图解中均落在酸性岩区。玄武质安山岩从新鲜岩石到其蚀变岩及其形成矿石的样品在Al_2O_3-Ti图解中均落在中基性岩-基性岩区。即不同蚀变程度的蚀变产物与其原岩在Al_2O_3-Ti图解中所在的区域一致,这表明新构建的Al_2O_3-Ti图解可以用来示踪蚀变岩的原岩性质。  相似文献   

2.
Coastal margins, especially the river-influenced coastal areas, are considered as active interfaces between the continental and oceanic environments, which have huge dispersal of detrital materials and heavy metal input. It is well determined that the fine-grained sediments are important reservoir for the accumulation of heavy metals. In this study, we analyzed the radiocarbon age, texture, organic matter, carbonate content, and geochemical compositions of two sediment cores (GM42 and GM44) retrieved in front of the Coatzacoalcos River mouth basin, southwestern Gulf of Mexico (～864 and 845 m water depth, respectively). Our objective was to infer the sedimentation rate, intensity of weathering, provenance, and influence of anthropogenic activities on heavy metal contamination in sediments. The radiocarbon-age measurements of mixed planktonic foraminifera for core GM44 reveals an age of 21,289 ± 136 cal. years B.P., which fall within the Late Glacial Maximum (LGM; 21000 ± 2000 years B.P). The calculated sedimentation rate for core GM42 (~0.013 cm/year) is lower than in core GM44 (0.022 cm/year), which is probably due to the variations in detrital sediment input and/or seafloor topography. The weathering indices such as chemical index of alteration (CIA), chemical index of weathering (CIW), and plagioclase index of alteration (PIA) suggested that the source area experienced low to moderate intensity of chemical weathering under warm to humid climatic conditions. The SiO2/Al2O3, Al2O3/Na2O, and K2O/Al2O3 ratio values indicated moderate to high compositional maturity. The major and trace element concentrations suggested that the sediments were likely derived from intermediate source rocks. The heavy metal contents indicated that the sediments were not contaminated by the industrial waste disposals supplied by the Coatzacoalcos River. The redox proxy sensitive elements such as V, Cr, Cu, and Zn indicated an oxic depositional environment for the deep-sea sediment cores. The application of discrimination diagrams for the geochemistry data revealed a passive margin setting for the sediment cores. The compositional variations observed at the upper sections (<30 cm) between the two sediment cores revealed that the type of detrital sediments supplied by the Coatzacoalcos River to the deep sea area is not uniform, which is also revealed by the variation in sedimentation rate.  相似文献   

3.
The geochemical study of the Dankar, Thinam and Gete lakes of the Spiti Valley has revealed that these lakes are characterized by varying contents of major ions, i.e. Ca, Mg, HCO3, Na, K, Cl, SO4, SiO2 and Sr as trace element. The concentration of these elements is significant, as they indicate the nature of the lithology and the type of weathering at the source. The sediment chemistry data have also been employed to quantify weathering intensity and to elucidate the provenance and basin tectonic setting where terrigenous sediment is deposited.Dankar Lake is located on the limestone-dolomite-rich Lilang Group of rocks (Triassic), and dissolution of carbonate is the prime source of ionic concentration in this lake. The high (Ca+Mg):HCO3 equivalent ratio of 6.94 indicates carbonate weathering, and the very low (Na+K):TZ+ ratio of 0.07, which is used as an indicator of silicate weathering, shows insignificant silica dissolution in this lake. On the other hand, in Lake Thinam a relatively low (Ca+Mg):HCO3 equivalent ratio of 2.09, a (Na+K):TZ+ ratio of 0.12 and other parameters indicate that carbonate is derived from calcareous nodules and thin intercalations of limestone in the Spiti shales (Jurassic), and also some contribution from silicate lithology is evident. Mixing of groundwater cannot be ruled out, as springs are observed in this lake. In Lake Gete, the (Ca+Mg):HCO3 equivalent ratio is again high at 5.04, and the (Na+K):TZ+ ratio is 0.15, indicating dissolution of both carbonate and silicate rocks in the basin. This is consistent with the corresponding lithology in the lakes, and their denudation. Very high Sr contents of 2,331 µg/l in Dankar Lake, 715 µg/l in Gete Lake and 160 µg/l in Thinam Lake are significant and support dissolution of carbonate rocks, as the silicate rocks contribute less Sr although its isotopic ratio is high. It is also reflected that mechanical erosion and chemical weathering are perhaps the effective processes in this region. The former exposes fresh mineral surface for dissolution. The chemical index of alteration (CIA), with an average value of 78.79 in Dankar and 81.06 in Gete, indicates high weathering conditions. The K2O–Fe2O3–Al2O3 triangular plots of the samples demonstrate residual clay formation, indicating intense weathering at the source. The clay mineralogical data corroborate the above observation.The sediment chemistry data document depletion in SiO2 and Al2O3, as they are enriched in carbonates and depleted in Na2O, K2O, MnO, and TiO2, as compared to PAAS and UCC which are related to strong weathering at the source. The positive linear correlation between K and Rb suggests that they are contained in the illitic phase, and high positive correlation of Zr and Y with SiO2 indicates their association with coarser-grain, quartz-rich sandstone. The high phyllosilicates and low feldspar and major element chemistry indicate recycling and mineral maturity of sediments deposited in the Tethyan basin in a passive margin setting. This also indicates older sedimentary-metasedimentary rocks which are ideally exposed in the Spiti Valley. The tectonic discriminant plots portray a passive margin tectonic setting of the detritus in these lakes.  相似文献   

4.
Two Holocene sediment cores were retrieved respectively from the enclosed Lake Daihai in the monsoon/arid transition zone of North China and the Taihu Lake coast in the monsoonal area of the Yangtze delta, Eastern China. Distribution of major geochemical elements and their ratios were employed to reveal the characteristics of Holocene climate and associated environmental implications in the two regions. It is suggested that the temporal distribution of major elements serve as a useful indicator to denote the variations of monsoon effective precipitation for the enclosed lake area. High values of resistant elements such as Al2O3, SiO2, TiO2, (FeO + Fe2O3), MnO in the lake sediments correspond to the depressed chemical weathering and weakened mon-soon effective precipitation, while the highs of mobile and easy soluble elements such as MgO, CaO, Na2O reflect the enhanced chemical weathering and increased monsoon effective precipitation in the lake basin. In comparison, the behaviors of the major elements in sediments of the Taihu Lake coast were largely controlled by the changes both in sea transgression in the different Holocene time periods and the monsoon precipitation. The relatively highs of Al2O3, TiO2, (FeO + Fe2O3), in marine-influenced sediments suggest relatively strong coastal hydrodynamics and chemical weathering, and vice versa. Meanwhile, the lows of SiO2, Na2O and CaO in the non-marine-influenced sediments also denote relatively strong hydrodynamics and chemical weathering due to enhanced monsoon precipitation, and vice versa. Sedimentary environment should be taken into account when achieving a full understanding of their climate implications.  相似文献   

5.
Pramod Singh   《Chemical Geology》2009,266(3-4):251-264
The sediments of the Ganga River from different depositional regimes in the Plain region such as the river channel, active flood-plain and the older flood-plain sediments from the inter-fluve region were analysed for major, trace and the rare earth elements (REEs). These are compared with catchment zone sediments of the river and probable source rocks in the Himalaya. The lower CIA values between 48 and 54.7 for the catchment sediments indicates that the sediments supplied to the Ganga Plain are chemically immature and subjected mostly to physical weathering due to higher erosion rates in the Himalaya. The CIA values ranging between 55 and 74, with average value of 59, 61.4 and 67 for sediments from the Plain's bed-load, active flood-plain and older flood-plain from the inter-fluve region indicates that silicate weathering of Ganga River sediments has occurred only after entering into the plains. This is likely because of higher residence time and change in the climate from cold-frigid in the Himalaya to tropical sub-humid in the plains. Therefore, the use of geochemical data on ancient system to infer climate in their source region may not always be true. Although the CIA values indicate a moderate chemical weathering in the plains, it is far from impressive. Dominance of physical weathering in the catchment region and lower degree of chemical weathering in the Plains indicate that weathering of sediments supplied by Himalayan Rivers, particularly the Ganga River may not have affected the atmospheric CO2 to a significant level as is generally believed. Thus the net effect of the Himalaya on the CO2 sequestration and consequent global cooling needs a re-evaluation.The plots of sediments in ternary diagram among La, Th, Sc and ratios involving Co/Th, La/Sc and Sc/Th indicate granitic to granodioritic source rocks to the sediments. The ratio plots involving relatively immobile Al2O3, TiO2 and FeO along with REE plots suggest that out of the major Himalayan lithologies, gneisses and Cambro-Ordovician granites of HHCS have acted as the dominant source to the sediments.The plots of LogNa2O/K2O vs. LogSiO2/Al2O3 and FeO/SiO2 vs. Al2O3/SiO2 diagrams show that the combination of processes including erosion, weathering, sorting and aeolian activity has together played a major role in progressively changing the chemistry from source rock to catchments bed-load to Plains bed-load, active flood-plains and the older inter-fluve sediments in the Ganga River system. The above plots demonstrate that as a result of above processes the ratios between the elements generally thought to be immobile and used in provenance studies does not always remain invariant and the linear trend line in the scatter gram between the two immobile elements show rotation around the fine grained end member.  相似文献   

6.
Pyrophyllite deposit at Madrangjodi is a large lensoidal massif overlain unconformably by Dhanjori quartzite and underlain by the parent Singhbhum granite (Phase — II). Pyrophyllite and quartz are the major minerals with minor to trace amounts of muscovite, chloritoid opaques and tourmaline. It is broadly divisible into lamellar, granular and schistose varieties. SiO2 (66.90–74.36%) and Al2O3 (20.80–27.54%) are the major oxides. The major elements data indicate its derivation from Singhbhum granite with depletion of SiO2 and increment of Al2O3. Trace and REE data are discussed to corroborate its genesis.  相似文献   

7.
Conventional graphical and statistical methods were used with water quality indices to characterize the hydrochemistry of groundwater from the northern part of the Volta region of Ghana. The objective was to determine the processes that affect the hydrochemistry and the variation of these processes in space among the three main geological terrains: the Buem formation, Voltaian System and the Togo series that underlie the area, and to determine the suitability of groundwater from the area for drinking purposes. The Q-mode cluster analysis reveals three main water groups. The groups established from the Q-mode HCA appear to indicate different degrees of weathering which could further indicate varying levels of fracturing aquifer hydraulic properties. R-mode HCA and factor analysis (using varimax rotation and Kaiser Criterion) were then applied to determine the significant sources of variation in the hydrochemistry. This study finds that groundwater hydrochemistry in the area is controlled by the weathering of silicate and carbonate minerals, as well as the chemistry of infiltrating precipitation. Mineral activity diagrams for the CaO–Na2O–Al2O3–SiO2–H2O and CaO–MgO–Al2O3–SiO2–H2O systems plotted for the area indicate stability in the smectite field and attribute hydrochemistry to the weathering of silicate minerals. Silicate mineral weathering and the effects of precipitation appear to be pervasive among all the three main geological terrains, whereas carbonate weathering is localized among the Voltaian aquifers. Cation exchange does not appear to play a significant role in the hydrochemistry but mild Water quality indices (WQI) were calculated for the samples using the concentrations of Na+, Ca2+, Mg2+, Cl−, NO3 −, F−, and EC at the various sample locations. The WQI values indicate that groundwater from the study area is of excellent quality for drinking purposes. WQI values from groundwater samples are averagely higher than samples taken from surface water sources in the area. This implies that geology has had an impact on the WQI of groundwater in the area.  相似文献   

8.
This study focuses on the Lower-Middle Miocene syn-orogenic flysch deposits of the Zoumi basin to infer source area paleoclimatic conditions, the intensity of source rocks paleoweathering, and mechanical sorting and recycling effects. The mudrocks are enriched in Al2O3, Fe2O3, CaO, and TiO2 relative to PAAS and depleted in the other mobile major elements. There are high positive correlations between SiO2, Al2O3, and TiO2 and negative correlations between SiO2 and CaO. Geochemically, the mudstones are mainly classified as shales, Fe-shales, and wackes. Various discriminant diagrams were used to reveal the inferred tectonics, source paleoweathering intensity, and paleoclimatic conditions. Chemical index of alteration (CIA) and chemical index of weathering (CIW) values for Lower-Middle Miocene vary from 50 to 80% indicating low to moderate degree of source area weathering compatible with non-steady-state weathering under wet and humid paleoclimatic conditions. Locally (Zoumi mid-section) CIA values are higher (>?80) reflecting intense source area weathering, which may be attributed to high tectonic impulses and more humid conditions during deposition. The combination of ICV-CIA, Al2O3-Zr-TiO2, and Th/Sc-Zr/Sc values suggests the bulk rock is chemically immature and has experienced modest physical sorting and recycling reflecting little transportation until the final deposition.  相似文献   

9.
River water composition (major ion and 87Sr/86Sr ratio) was monitored on a monthly basis over a period of three years from a mountainous river (Nethravati River) of southwestern India. The total dissolved solid (TDS) concentration is relatively low (46 mg L−1) with silica being the dominant contributor. The basin is characterised by lower dissolved Sr concentration (avg. 150 nmol L−1), with radiogenic 87Sr/86Sr isotopic ratios (avg. 0.72041 at outlet). The composition of Sr and 87Sr/86Sr and their correlation with silicate derived cations in the river basin reveal that their dominant source is from the radiogenic silicate rock minerals. Their composition in the stream is controlled by a combination of physical and chemical weathering occurring in the basin. The molar ratio of SiO2/Ca and 87Sr/86Sr isotopic ratio show strong seasonal variation in the river water, i.e., low SiO2/Ca ratio with radiogenic isotopes during non-monsoon and higher SiO2/Ca with less radiogenic isotopes during monsoon season. Whereas, the seasonal variation of Rb/Sr ratio in the stream water is not significant suggesting that change in the mineral phase being involved in the weathering reaction could be unlikely for the observed molar SiO2/Ca and 87Sr/86Sr isotope variation in river water. Therefore, the shift in the stream water chemical composition could be attributed to contribution of ground water which is in contact with the bedrock (weathering front) during non-monsoon and weathering of secondary soil minerals in the regolith layer during monsoon. The secondary soil mineral weathering leads to limited silicate cation and enhanced silica fluxes in the Nethravati river basin.  相似文献   

10.
黔北务川瓦厂坪铝土矿床元素迁移规律研究   总被引：6，自引：0，他引：6  
金中国 《地质与勘探》2011,47(6):957-966
黔北务正道地区铝土矿矿床属古风化壳沉积型,成矿母岩具多源性,但主要来源于下覆的中下志留统韩家店组。本文依据Grant提出的质量平衡方程和图解法,对瓦厂坪矿床在成矿过程中元素迁移的富集、贫化（亏损）规律进行了定量研究。结果表明,主要成矿母岩韩家店组砂、页岩一中间产物铝土质页岩、粘土岩是主要元素A12O3、TiO2显著富集...  相似文献   

11.
Major element compositions of 36 bulk samples and 41 clay samples, which were obtained from 47 topsoils collected in monsoonal eastern China, were investigated with conventional wet chemistry and X-ray fluorescence (XRF) spectrometry, respectively. Based on major element analyses, the mobility of major elements and latitudinal distributions of SiO2/Al2O3 ratio, chemical index of alteration (CIA), chemical index of weathering (CIW) and weathering index of Parker (WIP) were analyzed. Meanwhile, the suitability of these chemical weathering indices to topsoils in monsoonal eastern China and its controls were discussed.These investigations indicate that Na, K, Ca, Mg, and Si are relatively depleted, while Mn, P, Fe and Ti are relatively enriched in topsoils of the study area by comparison with their contents in the upper continent crust (UCC), and that alkali metal (Na, K) and alkaline earth metal (Ca, Mg) elements are generally easier to be depleted from their parent materials than other major elements during chemical weathering. The latitudinal distributions of CIA, CIW and WIP show that they are suitable to both bulk and clay samples, but SiO2/Al2O3 is only suitable to clay samples, not suitable in bulk ones. All these investigations indicate a significant dependence of grain-size in major element abundance and latitudinal distributions of SiO2/Al2O3, CIA, CIW and WIP, but parent rock type has little effect on them, except its impact on the latitudinal distribution of WIP in clay samples. The significant grain-size dependence probably indicates the presence of unaltered minerals in bulk samples, thus we suggest that clay samples are more suitable to investigating chemical weathering of sediments on continents than bulk samples. The trivial effect of parent rock type probably indicates a relatively uniform chemical weathering on various parent rocks. Correlation analyses indicate that climate is the dominant control of chemical weathering of topsoils in the study area, and the significant latitude effect indicated by the spatial distributions of chemical weathering indices actually reflect the climate control on chemical weathering of topsoils.Chemical weathering indices actually reflect the integrated weathering history in the study area. Besides the dominant control of climate, other factors like tectonics, parent rock, biology, landform and soil depth and age might also have some effect on the chemical weathering of topsoils in the study area, which needs further research.  相似文献   

12.
The Beypazarı granitoid in central Anatolia was emplaced during the Late Cretaceous and it is partly covered with Early Miocene–Quaternary sedimentary and volcanic units. Compression and tension regimes of the Beypazarı granitoid emplacing along the Sakarya River were evaluated considering the kinematical characteristics of discontinuities on granitoids, petrographic/geochemical works, formation of geothermal spring and irregularities in topographic structure. It was determined that the Beypazarı granitoid was witnessed with NE–SW compressional stress and NW–SE extensional stress which resulted in the formation of the Kapullu normal fault with N55–72°E, 78°SE crossing the Kapullu spring site. There are also several other probable normal faults around this fault in the Sakarya River basin. The results of the geochemical studies reveal that SiO2, Na2O, Al2O3, CaO and K2O as a major oxide and As, Rb, Sr, Th and U as trace elements are decreased away from the Kapullu bath spring. On the other hand, the ratio of Fe2O3 and MgO as major oxide and Y as a trace element with the lost on ignition (LOI) are increased away from the Kapullu fault. Regard as the regional plate tectonism, there is a consistency between the direction of compression in the Beypazarı granitoid and that developed by the southwesterly movement of the Anatolian plate.  相似文献   

13.
 One of the main uncertainties in mineralogical models of the Earth's lower mantle is the nature of the aluminous mineral: it is not clear whether Al forms its own minerals or is mainly contained in (Mg,Fe)SiO3-perovskite. This question is very important, since it is known that if Al were mainly hosted by perovskite, it would radically change Fe/Mg-partitioning and phase equilibria between mantle minerals, and also alter many physical and chemical properties of perovskite, which is currently believed to comprise ca. 70% of the volume of the lower mantle. This, in turn, would require us to reconsider many of our geochemical and geophysical models for the lower mantle. This work considers the possibility of a V3O5-type structured modification of Al2SiO5 to be the main host of Al in the lower mantle, as proposed by previous workers. We report ab initio calculations, based on density functional theory within the generalised gradient approximation (GGA) with plane wave basis set and nonlocal pseudopotentials. We consider polymorphs of Al2SiO5 (kyanite, andalusite, sillimanite, and hypothetical V3O5-like and pseudobrookite-like phases), SiO2 (stishovite, quartz) and Al2O3 (corundum). Computational conditions (e.g., plane-wave energy cutoff, Brillouin zone sampling) were carefully chosen in order to reproduce small energy changes associated with phase transitions between the Al2SiO5 polymorphs. Good agreement of crystal structures, bulk moduli, atomisation energies and the phase diagram of Al2SiO5 with experimental data was found. Strong disagreement between the calculated lattice parameters and density of V3O5-like phase of Al2SiO5 and experimental values, assigned to it by previous workers, suggests that a V3O5-structured phase of Al2SiO5 was never observed experimentally. In addition, we found that the most stable high-pressure assembly in Al2SiO5 system is corundum+stishovite, and the value of the transition pressure at T = O K (113 kbar) is in excellent agreement with experimental estimates (95–150 kbar). We explain the instability of octahedrally coordinated silicates of Al to decomposition on the basis of Pauling's second rule. Received: 18 May 1999 / Accepted: 5 November 1999  相似文献   

14.
In the present study, the lake floor sediments of the Karlad lake, located at higher elevation in Wayanad region of north Kerala, were analyzed for textural characteristics, organic matter, calcium carbonate, major oxides and trace elements. This study was carried out to infer the chemical composition, provenance and intensity of chemical weathering of the source rocks in the lake catchment area. Textural studies signify that lake floor sediments are predominantly as clays (38.75%) followed by sand (36.36%) and silt (25.19%) fractions. The C/N ratio of the lake sediments signify that the sediments are both autochthonous and allochthonous in origin. The major oxides average content reveals the order of abundance as follows; SiO2 > Al2O3 > Fe2O3 > TiO2 > MgO > CaO > K2O > P2O5 > Na2O > MnO. Moreover, the various weathering indices such as Chemical Index of Alteration (CIAAvg. 93.5%), PlagioclaseIndex of Alteration (PIA- Avg. 95.6%) and Chemical Index of Weathering (CIW- Avg. 95.76%) suggest an intense chemical weathering of the source area. The A-CN-K diagram is also corroborating the same. Various provenance discrimination diagrams reveal that the sediments are derived from the mafic source rocks.  相似文献   

15.
云南龙街盆地第四纪沉积及环境演化   总被引：5，自引：0，他引：5  
文章记述了云南龙街盆地龙街组湖相粉砂层的特征、形成环境及地层时代,并讨论了龙街粉砂层和泥石流堆积的相变关系及其发育规律。对广布于龙街盆地的红土风化壳的化学性质、类型、时代及其所反映的气候环境进行了分析。在此基础上着重讨论了龙街盆地自中—晚更新世以来的湖盆变迁、沉积规律及气候环境特征。  相似文献   

16.
IIb trioctahedral chlorite in the Barberton greenstone belt (BGB) metavolcanic rocks was formed during pervasive greenschist metamorphism. The chem‐ical composition of the chlorite is highly variable, with the Fe/(Fe+Mg) ratio ranging from 0.12 to 0.8 among 53 samples. The chemical variation of the chlorite results from the chemical diversity of the host rock, especially the MgO content of the rock, but major details of the variation pattern of the chlorite are due to the crystal structure of the chlorite. All major cation abundances in the chlorite are strongly correlated with each other. Sil‐icon increases with Mg and decreases with Fe, while AlIV and AlVI decrease with Mg and increase with Fe2+. A complex exchange vector explains over 90% of the chlorite compositional variation: Mg4SiFe2+ −3AlVI −1 AlIV −1, which has 3 parts Fe-Mg substitution coupled with one part tschermakite substitution. This ratio is required to maintain the charge and site balances and the dimensional fit between the tetrahedral and octahedral sheets. The subtle change in Al substitution in chlorite implies that AlVI is preferentially ordered in the M(4) site, and about 84% of the AlVI present is in the M(4) sites when they are nearly filled with AlVI. Based on 47 analyzed chlorite-bearing rock samples, chlorite (Chl) composition is strongly correlated with the MgO content of the host rock. Calculated correlation coefficients are +0.91 for SiO2Chl-MgORock, −0.87 for Al2O3Chl-MgORock, +0.89 for MgOChl-MgORock, and −0.85 for FeOChl-MgORock. Only weak correlations have been found between chlorite oxides and other oxides of rock (between same oxides in chlorite and rock: SiO2−0.67, Al2O3 + 0.59, FeO −0.41). However, MgOChl is saturated at about 36 wt% in rocks that have MgO above 22 wt%.The MgOChl is about 5 wt% when the host rock approaches 0 wt% of MgO. This implies that Mg substituting into the chlorite is approximately limited to 1.5–9.2 Mg atoms per formula unit and 1.0–3.2 AlIV. Chlorite geothermometers can not be applied to all BGB samples. However, the empirical chlorite geothermometer based on AlIV of chlorite may be applicable to chlorites formed under metamorphic conditions because it can predict the chemical composition of the chlorite from basaltic and dacitic samples in this study. An estimated temperature of about 320°C for the greenschist metamorphism of the greenstone belt through this geothermometer is consistent with that obtained by other geothermometers. Received: 22 January 1996 / Accepted: 15 August 1996  相似文献   

17.
On cursory examination of hand specimens and thin sections, the abyssal tholeiite in a dredge haul may appear to be uniform in composition. Chemical analyses of a considerable number of fragments, however, have always revealed the existence of regular compositional variation in them. The MgO content decreases with increasing SiO2. In abyssal tholeiites with relatively low Al2O3 contents, the SiO2, total iron, Na2O and P2O5 contents tend to increase and the MgO content tends to decrease with increasing iron/magnesia ratio, probably owing to crystallization differentiation.In a certain dredge haul, high-alumina abyssal tholeiites (with Al2O3 contents near or over 17%) occur in association with low-alumina abyssal tholeiites. The magma of high-alumina abyssal tholeiites would be generated from that of low-alumina abyssal tholeiites by differentiation at a depth around 30 km.In pillow lavas of abyssal tholeiite free from weathering and metamorphism, the chilled rim of the pillow usually has virtually the same chemical composition as the more crystalline core except for a decrease of K2O content toward the rim. On the other hand, the weathered rim of pillow lavas shows marked compositional change. The Fe2O3/FeO ratio of unweathered abyssal tholeiite is in the range of 0.1 to 0.3. This ratio and the H2O– and H2O+ contents increase with advancing weathering.Lamont-Doherty Geological Observatory Contribution No. 1339  相似文献   

18.
A. A. Borisov 《Petrology》2009,17(6):579-590
The simultaneous saturation of silicate melts with variable Al2O3 and SiO2 contents in sodium, potassium, and rubidium was investigated at a total pressure of 1 atm and temperatures of 1300–1470°C using the crucible supported loop technique. It was shown that an increase in both SiO2 and Al2O3 contents in the melt results in a significant decrease in the activity coefficients of the alkalis, and the effect of Al2O3 is especially pronounced in silicic compositions. The extrapolation of the experimental data allowed us to estimate the influence of SiO2 and Al2O3 contents in the melt on the behavior of Li and Cs. Using a numerical experiment, it was shown how the inert and perfectly mobile behavior of alkalis in magmatic processes can be discriminated. A methodic investigation was performed on the loss of Na, K, and Rb from silicic glasses during microprobe analysis depending on beam diameter.  相似文献   

19.
The heat capacity and vibrational entropy of a calcium aluminate and three peraluminous calcium aluminosilicate glasses have been determined from 2 to 300 K by heat-pulse relaxation calorimetry. Together with previous adiabatic data for six other glasses in the system CaO-Al2O3-SiO2, these results have been used to determine partial molar heat capacities and entropies for five species namely, SiO2, CaO and three different sorts of Al2O3 in which Al is 4-, 5- and 6-fold coordinated by oxygen. Given the determining role of oxygen coordination on low-temperature heat capacity, the composition independent entropies found for SiO2 and CaO indicate that short-range order around Si and Ca is not sensitive to aluminum speciation up to the highest fraction of 25% observed for VAl by NMR spectroscopy. Because of the higher room-temperature vibrational entropy of IVAl2O3 (72.8 J/mol K) compared to VAl2O3 (48.5 J/mol K), temperature-induced changes from IVAl to VAl give rise to a small negative contribution of the order of 1 J/mol K to the partial molar configurational heat capacity of Al2O3 in melts. Near 0 K, pure SiO2 glass distinguishes itself by the importance of the calorimetric boson peak. On a g atom basis, the maximum of this peak varies with the composition of calcium aluminosilicate glasses by a factor of about 2. It does not show smooth variations, however, either as a function of SiO2 content, at constant CaO/Al2O3 ratio, or as a function of Al2O3 content, at constant SiO2 content.  相似文献   

20.
In this study, an assessment of the lithogenic concentrations of trace metals in soils and saprolite over basement rock units in Ibadan, SW-Nigeria is presented in respect of bedrock types and geochemical controls on the weathering-associated release of trace metals. Consequently, soil, weathered and fresh rock samples from the Precambrian Basement of SW Nigeria were collected from three different bedrock units within Ibadan metropolis and subjected to mineralogical and geochemical analyses. The analytical results revealed major proportions of oxides in the range of 18–20% Al2O3, 2–6% Na2O and 1–6% K2O for weathered profiles over granite-gneiss and pegmatite units, compared to 2–3% Al2O3, <0.5% Na2O and <1.0% K2O over schist-quartzite. For the trace elements, weathered profiles on granite-gneiss and schist-quartzite settings exhibit similar enrichment trends (enrichment factor, EF l) for most of the trace elements, unlike the pegmatite bedrock. However, enrichments are relatively greater in the top soil unit compared to the intermediate saprolite unit, especially for Pb, Ni, Zn, Cr, Co, Rb, Sr and Ba, a situation attributed to leaching and redistribution within the weathered profiles through pedogenetic process and percolating groundwater.Furthermore, the estimated weathering indices using Ruxton Ratio (RR = {SiO2/Al2O3}) and Chemical Index of Alteration (CIA = 100{Al2O3/[Al2O3 + CaO + Na2O + K2O]}) revealed RR of 2.9–3.7 and CIA of 54–73% for granite-gneiss and pegmatite units, implying medium levels of weathering, compared to RR of 30.8–35.5 and CIA of >60% for schist-quartzite units, which suggest weak chemical weathering. Also, the estimated high percentage loss, especially for Pb, Rb, Sr, Ba relative to the bedrocks, shows that the trace elements can be mobilized within the weathering profiles even at a low degree of chemical weathering. Such weathering-induced release of trace metals is of environmental significance as natural lithogenic input sources and as background reference for future monitoring of possible human/anthropogenic impacts.  相似文献   

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