Geochemical and palynological analyses of the Serikagni Formation, Sinjar, Iraq

Serikagni Formation (lower–middle Miocene) was studied at four outcrop sections within Sinjar Anticline, Para (the western plunge), Jaddala, Sinjar, (Southern limb), and Noaniaa (Northern limb) of Sinjar Mountain, which is part of foothill zone in northwest Iraq. This formation is composed of Globigerina limestone, marly limestone intercalated with marl, deposited in quiet, deep marine environment. Palynological analyses and the percentages of palynological matter were determined. Palynofacies analysis was recorded for paleoenvironmental interpretation. Mineralogical investigations and petrographical analyses were done. Geochemical analyses for the determination of the major constituents (CaO, MgO, and I.R.),the secondary constituents (SiO₂, Al₂O₃, Fe₂O₃, Na₂O, K₂O, and trace elements (Sr, Mn, Cu, Zn, Co, Cr, Pb) in the rock samples were accomplished. The calcite is the predominant mineral which is mostly of micrite types as well as spary calcite. The insoluble residue (I.R.) has negative correlation with the carbonate percentages in the rock formation as observed by the XRD analyses. Clay minerals show low occurrence represented by palygorskite, montmorillonite, and sepiolite. Geochemical differences can be noticed between the limy and marly facies constituting the same formation. Differences are also observed between the geochemistry and mineralogy of the four studied localities such as the relatively more pure limestone in Jaddala and Para sections than Sinjar and Noaniaa sections which indicate the higher percentages of marly limestone. This is believed to be due to the geographic location of these sections within the main depositional environment, as well as the consequences of sea level fluctuation. Two palynofacies (PF-1) and (PF-2) were identified. Palynomorphs are more numerous with high percentages (>80%) of amorphous organic matter (AOM) is present in the PF-1. The lithological association of this palynofacies is limestone and marly limestone. This palynofacies 1, indicate the deep marine depositional environment. The second palynofacies (PF-2) reflect low quantities (less than 40%) of AOM, with increase of phytoclasts (translucent-type) to more than 30% and the miospores (small spores and pollen grains) to more than 20%. The lithological association of this palynofacies is marl and marly limestone. This palynofacies 2, indicate the nearshore and shallow marine depositional environment.     

Progressive evolution of whole‐rock composition during metamorphism revealed by multivariate statistical analyses

The geochemical evolution of metamorphic rocks during subduction‐related metamorphism is described on the basis of multivariate statistical analyses. The studied data set comprises a series of mapped metamorphic rocks collected from the Sanbagawa metamorphic belt in central Shikoku, Japan, where metamorphic conditions range from the pumpellyite–actinolite to epidote–amphibolite facies. Recent progress in computational and information science provides a number of algorithms capable of revealing structures in large data sets. This study applies k‐means cluster analysis (KCA) and non‐negative matrix factorization (NMF) to a series of metapelites, which is the main lithotype of the Sanbagawa metamorphic belt. KCA describes the structures of the high‐dimensional data, while NMF provides end‐member decomposition which can be useful for evaluating the spatial distribution of continuous compositional trends. The analysed data set, derived from previously published work, contains 296 samples for which 14 elements (Si, Ti, Al, Fe, Mn, Mg, Ca, Na, K, P, Rb, Sr, Zr and Ba) have been analysed. The KCA and NMF analyses indicate five clusters and four end‐members, respectively, successfully explaining compositional variations within the data set. KCA indicates that the chemical compositions of metapelite samples from the western (Besshi) part of the sampled area differ significantly from those in the east (Asemigawa). In the west, clusters show a good correlation with the metamorphic grade. With increasing metamorphic grade, there are decreases in SiO₂ and Na₂O and increases in other components. However, the compositional change with metamorphic grade is less obvious in the eastern area. End‐member decomposition using NMF revealed that the evolutional change of whole‐rock composition, as correlated with metamorphic grade, approximates a stoichiometric increase of a garnet‐like component in the whole‐rock composition, possibly due to the precipitation of garnet and effusion of other components during progressive dehydration. Thermodynamic modelling of the evolution of the whole‐rock composition yielded the following results: (1) the whole‐rock composition at lower metamorphic grade favours the preferential crystallization of garnet under the conditions of the garnet zone, with biotite becoming stable together with garnet in higher‐grade rock compositions under the same P–T conditions; (2) with higher‐grade whole‐rock compositions, more H₂O is retained. These results provide insight into the mechanism suppressing dehydration under high‐P metamorphic conditions. This mechanism should be considered in forward modelling of the fluid cycle in subduction zones, although such a quantitative model has yet to be developed.     

Chemical analyses of Bosumtwi crater target rocks compared with the Ivory Coast tektites

The Bosumtwi crater, Ghana, was excavated in phyllites and greywackes with subordinate microgranite dykes and quartz veins of the 2000 Ma old Lower Birimian System with a granodiorite intrusion at Pepiakese on its northeastern side. New major and trace element analyses are presented for 7 phyllites, 5 greywackes, 2 microgranites, 3 Pepiakese intrusion rocks and 1 suevite using XRF and INNA.Means and standard deviations were calculated using all available modern analyses for each element in the Bosumtwi target rocks, Bosumtwi suevite glasses and Ivory Coast tektites. Good agreements between the means were found for the three groups with the suevite glasses and tektites having more limited compositional ranges than the target rocks. Least squares mixing between target rock types shows that the best fits to the tektite and suevite glass compositions require components of about a third or a quarter from the Pepiakese intrusion and some extra silica, derived from quartz veins, as well as the metasediments.The new data provide evidence for vapour phase fractionation of P₂O₅ and Na₂O in the tektites in addition to the previously reported Pb and Rb. Evidence for a meteoritic component in the tektites was found to be equivocal since the target rocks are probably a sufficient source of the meteorite indicator elements Ni and Ir.     

The crystal chemistry of mordenites

Mordenite is a zeolite whose approximate composition is (Na₂, K₂,Ca)₄[Al₈Si₄₀O₉₆] 28 H₂O. Unit cell dimensions, determined by X-ray powder diffractometry for 35 natural samples, fell within the following ranges: a=18.052–18.168, b=20.404–20.527, c=7.501–7.537 Å. The indexed powder pattern of a typical sample is reported. Complete wet chemical analyses of 12 samples, partial analyses of three others, and 6 analyses from the literature reveal that mordenites vary only slightly in chemical composition. Si occupies 80 to 85% of the tetrahedra, and the exchangeable cations are mainly Na and Ca, with minor K. The lattice constant b is negatively correlated to the ratio Si/(Si+Al+Fe?).     

Origins and evolution of rhyolitic magmas in the central Snake River Plain: insights from coupled high-precision geochronology,oxygen isotope,and hafnium isotope analyses of zircon

We present new high-precision CA-ID-TIMS and in situ U–Pb ages together with Hf and O isotopic analyses (analyses performed all on the same grains) from four tuffs from the 15?10 Ma Bruneau–Jarbidge center of the Snake River Plain and from three rhyolitic units from the Kimberly borehole in the neighboring 10?6 Ma Twin Falls volcanic center. We find significant intrasample diversity in zircon ages (ranges of up to 3 Myr) and in δ¹⁸O (ranges of up to 6‰) and ε_Hf (ranges of up to 24 ε units) values. Zircon rims are also more homogeneous than the associated cores, and we show that zircon rim growth occurs faster than the resolution of in situ dating techniques. CA-ID-TIMS dating of a subset of zircon grains from the Twin Falls samples reveals complex crystallization histories spanning 10⁴–10⁶ years prior to some eruptions, suggesting that magma genesis was characterized by the cyclic remelting of buried volcanic rocks and intrusions associated with previous magmatic episodes. Age-dependent trends in zircon isotopic compositions show that rhyolite production in the Yellowstone hotspot track is driven by the mixing of mantle-derived melts (normal δ¹⁸O and ε_Hf) and a combination of Precambrian basement rock (normal δ¹⁸O and ε_Hf down to ??60) and shallow Mesozoic and Cenozoic age rocks, some of which are hydrothermally altered (to low δ¹⁸O values) by earlier stages of Snake River Plain magmatism. These crustal melts hybridize with juvenile basalts and rhyolites to produce the erupted rhyolites. We also observe that the Precambrian basement rock is only an important component in the erupted magmas in the first eruption at each caldera center, suggesting that the accumulation of new intrusions quickly builds an upper crustal intrusive body which is isolated from the Precambrian basement and evolves towards more isotopically juvenile and lower-δ¹⁸O compositions over time.     

Geochemistry of rock units at the potential repository level,Yucca Mountain,Nevada

The compositional variability of the phenocryst-poor member of the 12.8 Ma Topopah Spring Tuff at the potential repository level was assessed by duplicate analysis of 20 core samples from the cross drift at Yucca Mountain, Nevada. Previous analyses of outcrop and core samples of the Topopah Spring Tuff showed that the phenocryst-poor rhyolite, which includes both lithophysal and nonlithophysal zones, is relatively uniform in composition. Analyses of rock samples from the cross drift, the first from the actual potential repository block, also indicate the chemical homogeneity of this unit excluding localized deposits of vapor-phase minerals and low-temperature calcite and opal in fractures, cavities, and faults. The possible influence of vapor-phase minerals and calcite and opal coatings on rock composition at a scale sufficiently large to incorporate these heterogeneously distributed deposits was evaluated and is considered to be relatively minor. Therefore, the composition of the phenocryst-poor member of the Topopah Spring Tuff is considered to be adequately represented by the analyses of samples from the cross drift. The mean composition as represented by the 10 most abundant oxides in wt.% or g/100 g is: SiO₂, 76.29; Al₂O₃, 12.55; FeO, 0.14; Fe₂O₃, 0.97; MgO, 0.13; CaO, 0.50; Na₂O, 3.52; K₂O, 4.83; TiO₂, 0.11; and MnO, 0.07.     

Die Glaukophangesteine,ihre stofflichen Äquivalente und Uniwandlungsprodukte in Nordcalabrien (Süditalien)

In the southern Apennin (= northern part of the region dealt with) and the Coasta Chain (= southern part) there are metabasalts wich are classified in the northern part as:

1. Glaucophane rocks of the albite-lawsonite-glaucophane-subfacies with the assemblage glaucophane + pumpellyite + lawsonite ±albite ±aragonite ±muscovite (7 rock analyses, 8 mineral analyses). These rocks are conceived as relics of an older burial metamorphism.
2. Rocks with pumpellyite and chlorite or also chlorite alone, that are interpreted as reaction rims between the metastable glaucophane rocks and the country rock (phyllites, quartzites). The assemblages pumpellyite + chlorite and chlorite alone are to be found (2 rock analyses and 2 mineral analyses).
3. Rocks with lawsonite and/or epidote belong to the same mineral facies as the country rock: a facies similar to the greenschist facies (called “lawsonite-albite-chlorite-subfacies”) which is characterized by the assemblages lawsonite + albite + chlorite ±calcite and also epidote ±lawsonite + albite + chlorite ± muscovite. These types are attributed to a younger dynamo-metamorphism (2 rock analyses).

In the southern part, the metabasalts can be found only as rocks with epidote and/or lawsonite, a metamorphism with more than one event cannot be proved petrologically (3 rock analyses). Equations of the observed mineral reactions are given. The transitions of one facies into another are represented in the pseudo-quaternary system Al₂O₃-CaO-Na₂O · Al₂O₃-2 Fe₂O₃ + FeO + MnO + MgO-(H₂O). The pressure-temperature conditions are estimated on the basis of published experimental data (300° C and 6–7 kb for the glaucophane rocks; 400° C and about 6 kb for the rocks with lawsonite and/or epidote) and are compared with geologic facts.     

Complete chemical analyses of metamorphic hornblendes: implications for normalizations,calculated H2O activities,and thermobarometry

Twenty-two hornblendes separated from amphibolites and granulites of the Grenville Orogen of Ontario have been quantitatively analyzed for major and minor elements by electron microprobe, for FeO/Fe₂O₃ by wet chemistry, and for H₂O by manometric measurement as H₂. Hornblende formulae were calculated on the basis of 24O+OH+Cl+F. Most samples are magnesio-hornblendes, ferroan pargasitic hornblendes and ferroan hastingsitic hornblendes, with weight fractions of Fe³⁺/(Fe²⁺+Fe³⁺) ranging from 0.15 to 0.50. An oxy-amphibole component of 0–25 mol%, with an average value of 17 mol%, is obtained for these complete analyses. When compared with structural formulae determined solely from microprobe data, normalization based on 13=Si+Ti+Al+Fe+Mn+Mg cations provides the best approximation to hornblende formulae calculated from the complete analyses. Less satisfactory agreement is obtained from a normalization scheme based on 15=Si+Ti+Al+Fe+Mn+Mg+Ca, while worst agreement is obtained from normalization to 23 oxygens assuming all Fe is Fe²⁺. No normalization scheme based on microprobe data alone consistently replicates the measured FeO, Fe₂O₃, and H₂O; accurate determination of these values requires complete chemical analysies. Ionic solution models previously have been proposed to evaluate the activity of Ca₂Mg₅Si₈ O₂₂(OH)₂(a _Trem) in hornblende for use in equilibria that constrain the activity of H₂O (a _{H 2}O) in igneous and metamorphic rocks. Application of ionic models to typical hornblendes produces low a _Trem (usually<0.01), consequetly yielding extremely low a _{H 2}O. If an oxy-amphibole component is present, the calculated a _Trem and H₂O is further reduced. An oxy-amphibole component of 25% reduces the calculated H₂O activity and that of any hydroxyl-amphibole component by 50% below that calculated with simplified assumptions regarding X _OH in the hydroxyl site (i.e., X _OH=1, or X _OH=1–X _Cl–X _f). Thus, methods of amphibole normalizations appear to have a substantial effect on calculated amphibole and H₂O activites. Before quantitative hornblende thermobarometry can be calibrated and applied, the amounts of FeO, Fe₂O₃ and H₂O must be measured in order to fully characterize hornblende solid solutions.Contribution No. 478 from the Mineralogical Laboratory, University of Michigan     

Mass transfer during sub-seafloor alteration of the upper Troodos crust (Cyprus)

Five major alteration zones in the Extrusive Series and the Sheeted Dike Complex of the Troodos Ophiolite are each characterized by (a) distinct elemental changes compared to the original composition and (b) secondary mineralogy. The upper ca. 300 m of the extrusive crust, the highly oxidatedcold seawater alteration zone (CSA), is strongly enriched in K₂O and depleted in Na₂O. It is followed downwards by alow temperature alteration zone (<170° C) which is most widespread in the Troodos extrusives and where Na₂O and K₂O are enriched, the latter less strongly than in the CSA zone. Three types ofhigh temperature alteration zones (<440° C; HTA I–III) are found in the Sheeted Dike Complex. All are marked by thorough leaching of K₂O, while the behavior of Na₂O (e.g. unchanged in type III) and CaO (depleted in type I, enriched in types II, III) is variable. Mass budgets of elemental changes are quantified by calibration of whole rock analyses via systematic stable element variations of fresh glasses found throughout the extrusive section. The Troodos extrusive crust and upper Sheeted Dike Complex are a major sink for MgO, K₂O, and Na₂O, and a source for CaO; the overall scale of fluxes drastically exceeds estimates based on fresh basalt compositions from present ocean crust.     

Calculated stabilities of sodic phases in the Sambagawa metapelites and their implications

Pressure (P)–temperature (T) pseudosection analyses were carried out on metapelites from Sambagawa belt by using Perple_X 07 so as to determine mineral equilibria and the stability of sodic phases, in the model system MnO–Na₂O–K₂O–CaO–FeO–MgO–Al₂O₃–SiO₂–H₂O–(CO₂) under high‐pressure (HP) conditions (0.5–2.5 GPa/400–600 °C). A pressure–X_NA [=Na/(Na+Al–2K–1.5Ca)] pseudosection at 500 °C is also calculated to examine the effect of Na/Al value of the bulk‐rock composition on the stabilities of sodic minerals. The bulk‐rock compositions of Sambagawa metapelite are variable in X_NA values. The calculation results of stable assemblages in metapelites under the blueschist and eclogite facies conditions indicate that: (i) paragonite and glaucophane are stable throughout the wide X_NA range of bulk‐rock compositions of host rocks; (ii) stable P–T conditions of sodic pyroxene enlarge with increasing X_NA value; and (iii) the stability field of paragonite enlarges with the presence of CO₂ in the metamorphic fluid. The suggested wide stability of paragonite in metapelites and the relationships between the stability of sodic pyroxene and the bulk‐rock compositions explain the reasons why (i) the occurrence of omphacite in metapelites from several subduction‐related terranes is rare; and (ii) paragonite commonly occurs as inclusions in garnet of metapelites from the Besshi region of the Sambagawa belt. Paragonite is an important sodic phase of HP metapelites, and a combination of paragonite and quartz with high residual pressure included in garnet may be a useful indicator to verify the evidence for the eclogite facies metamorphism recorded in metapelites.     

Calcic hydrosilicate metasomatic rocks at the Gumeshevsk skarn-porphyry copper deposit in the central Urals,Russia

The body of hydroxylellestadite metasomatic rock penetrated by a borehole drilled at the Gumeshevsk deposit at depths of 530–534 m includes a thin interval of younger lower temperature tobermorite-plombierite metasomatic rock with subordinate amounts of Ca-Si gel, tacherenite, cubic lime, and thaumasite. Hydroxylellestadite has never before been found in calc skarns. The hydroxylellestadite metasomatic rock is cut by gypsum and fukalite veinlets, and the tobermorite-plombierite metasomatic rock is intersected by thaumasite veinlets. The pristine rock of the metasomatics was marble, and the metasomatic rock replaced andradite-bearing wollastonite skarn (with wollastonite replaced by foshagite). The ore minerals (chalcopyrite, valleriite, sphalerite, and others) were formed after the hydroxylellestadite metasomatite but most probably before the tobermorite-plombierite metasomatic rock and the veinlets of calcic minerals. The metasomatic rock was produced at significant variations in the oxygen, sulfur, and carbon dioxide fugacities. The composition of the hydroxylellestadite is, according to its microprobe analysis, as follows (wt %): SiO₂ 17.10, TiO₂ 0.01, Al₂O₃ 0.02, FeO 0.20, MnO 0.00, MgO 0.04, CaO 55.40, Na₂O 0.14, K₂O 0.09, P₂O₅ 0.12, CO₂ 1.90 (chemical analysis), SO₃ 21.60, F 0.16, Cl 0.14, total 96.92. The plombierite (SiO₂ 43.8–44.1 wt %, CaO 30.5–31.1 wt %) in the metasomatic rock notably differs from rare plombierite (SiO₂ 48.18 wt %, CaO 39.19 wt %) contained in the veinlets of thaumasite (SiO₂ 12.70 wt %, CaO 30.69 wt %, SO₃ 17.78 wt %).     

基于电子探针面扫描定量化的石英闪长岩微区成分分析

岩石的微区成分特征是精细化反演岩石演化的重要依据,而常规的电子探针面扫描分析方法无法提供面扫描区域的定量分析结果.本文使用矿物分布相对均匀的代表性岩石样品开展了岩石薄片的面扫描和矿物的定量分析.通过对常规测试的主量元素的面扫描进行图像校正,并利用ZAF校正后的点分析数据与面扫描图像的灰度值进行最小二乘法曲线拟合的方式,...     

Water content of a granite magma deduced from the sequence of crystallization determined experimentally with water-undersaturated conditions

The sequence of crystallization in a biotite-granite from the Bohus batholith of Norway and Sweden, deduced from its texture, was magnetite, plagioclase, microcline, quartz, and finally biotite. Several sequences of crystallization were determined experimentally at 2 kb in the presence of varying only for H₂O contents below 1.2% by weight. The rock was fused to a homogeneous glass, and each experiment included samples of finely crushed rock and glass. The samples were reacted in Ag-Pd capsules with measured H₂O content in coldseal pressure vessels with NNO buffer. With excess H₂O (more than 6.5%) the crystallization interval extends from 865° C to 705° C. In the H₂O-deficient region, the solidus temperature remains unchanged as long as a trace of vapor is present, but the liquidus temperature increases as H₂O content decreases; with 0.8 % H₂O the liquidus temperature is 1125° C, the crystallization interval is 420° C, and a separate aqueous vapor phase is evolved only a few degrees above the solidus at 705° C. The biotite phase boundary increases slightly from 845° C with excess H₂O to 875° C with 1% H₂O, and it intersects the steep phase boundaries for quartz and feldspars; the sequence of crystallization changes at each intersection point. Similar diagrams at various pressures for related rock compositions involving muscovite, biotite and amphibole will provide grids useful in defining limits for the water content of granitic and dioritic magmas. Applications are considered for the Bohus batholith, other granitic rocks, and rhyolites. The Bohus magma could have been formed by crustal anatexis as a mobile assemblage of H₂O-undersaturated liquid and residual crystals with initial total H₂O content less than 1.2%, or it could have been derived by fractionation of a more basic parent with low H₂O content from mantle or subduction zone, but it could not have been derived from a primary andesite generated from mantle peridotite. We consider it unlikely that the H₂O content of large granitic magma bodies exceeds about 1.5% H₂O; these magmas are H₂O-undersaturated through most of their histories. Uprise and progressive crystallization of magma bodies produces H₂O-saturation around margins and in the upper regions of magma chambers. H₂O-saturated rhyolitic and dacitic magmas with phenocrysts can be tapped from the upper parts of the magma chambers.     

The major‐ and trace‐element whole‐rock fingerprints of Egyptian basalts and the provenance of Egyptian artefacts

Discrimination diagrams have been developed that source Egyptian basaltic artefacts using whole‐rock major element geochemistry. These include K₂O versus SiO₂, TiO₂ and P₂O₅ against MgO/Fe₂O₃^t (total Fe as Fe₂O₃), and a discriminant analysis diagram using SiO₂, Fe₂O₃^t, CaO, and MnO. A complementary set of diagrams uses easily obtained trace element data (Nb/Y versus Zr/Nb; Zr [ppm] versus Rb/Sr; TiO₂ [wt % volatile free] versus V; and Cr [ppm] versus Zr/Y) to determine the bedrock sources. These diagrams have been applied to seven First Dynasty basalt vessels (Abydos), two Fourth Dynasty basalt paving stones (Khufu's funerary temple, Giza), and two Fifth Dynasty paving stones (Sahure's complex, Abu Sir). They show that the bedrock source for all the artefacts was the Haddadin flow in northern Egypt. Multidimensional scaling and cluster analysis applied to the whole‐rock data (major elements and trace elements together) and previously published mineral fingerprinting studies confirm these results. Comparing mineral versus whole‐rock fingerprinting techniques, a major advantage of the former is the small sample size required (0.001 g compared to ≥ 0.1 g). Analytical costs are similar for both methods assuming that a comparison (bedrock) database can be assembled from the literature. For most archaeological problems, a whole‐rock bedrock database is more likely to exist than a mineral database, and whole‐rock analyses on artefacts will generally be easier to obtain than mineral analyses. Whole‐rock fingerprinting may be more sensitive than mineral‐based fingerprinting. Thus, if sample quantity is not an issue, whole‐rock analysis may have a slight cost, convenience, and technical advantage over mineral‐based methods. Our results also emphasize that the Egyptians cherished their Haddadin basalt flow and used it extensively and exclusively for manufacturing basalt vessels and paving stones for at least 600 years (∼3150 B.C. to 2500 B.C., approximate ages of the vessels and Abu Sir paving stones, respectively). © 2001 John Wiley & Sons, Inc.     

H2O in metamorphism and unexpected behaviour in the preservation of metamorphic mineral assemblages

The preservation of mineral assemblages that were fluid‐present during their prograde history is primarily related to the consumption of the fluid by growth of more hydrous minerals as the retrograde history begins. The range of behaviour relating to the preservation of mineral assemblages is examined using calculated phase diagrams for fluid‐saturated conditions, contoured for the H₂O content of the mineral assemblage. At equilibrium, as a mineral assemblage crosses contours of decreasing H₂O content along a pressure–temperature path, it dehydrates, the fluid being lost from the rock. If the assemblage crosses contours of increasing H₂O content, the mineral assemblage starts to rehydrate using any fluid on its grain boundaries. When the rock has consumed its fluid, the resulting mineral assemblage is that preserved in the rock. Conditions relating to the preservation of mineral assemblages are discussed, and examples of the consequences of different pressure–temperature paths on preservation in a metapelitic and a metabasic rock composition are considered on phase diagrams calculated with thermocalc .     

Compositional Variation of Hydrothermally Altered Volcanic Rocks in Hishikari Gold Epithermal System: A Useful Geochemical Indicator of Gold–Silver Epithermal Mineralization

The hydrothermally altered andesite hosting the Hishikari gold-silver vein deposits in southern Kyushu, Japan, is analyzed with respect to the spatial variation in chemical composition. The (CaO + Na₂O) content is found to be inversely correlated with the K₂O content as it progresses away from the site of mineralization. It was found that analytical data plotted on a (CaO + Na₂O) − K₂O diagram cannot be explained only by addition of K⁺ from the hydrothermal solution to the original rock and release of Ca²⁺ and Na⁺ from the original rock (K- alteration). Addition of Ca²⁺ and Na⁺ from the hydrothermal solution to the rock and release of K⁺ from the rock but release of K⁺, Ca²⁺, and Na⁺ to the hydrothermal solution (advanced argillic alteration) is important for causing the wide variations in K₂O, CaO, and Na₂O contents on the (CaO + Na₂O) − K₂O diagram. These variations can be explained by superimposed potassic, advanced argillic and calcium alterations. The altered rocks in the Honko-Sanjin area, Yamada area, and Masaki area analyzed by this study are characterized by their intermediate K₂O content and variable CaO content, high K₂O content and low CaO content, and low K₂O content and low CaO content, respectively. The K₂O, Na₂O and CaO contents and oxygen isotopic composition of altered andesite, in conjunction with the solubility of gold as a thio complex, suggest that both gold deposition and the observed compositional variation of altered andesite are the result of mixing between acidic groundwater and neutral gold-bearing hydrothermal solution. The present results indicate that the compositional variation of hydrothermally altered rocks may represent a useful geochemical indicator of epithermal gold–silver mineralization.     

河北东坪金矿区水泉沟岩体的地球化学特征

水泉沟岩体主要由二长岩构成。主要矿物是碱性长石和斜长石,它们的含量高达80%以上。石英不多见,暗色矿物含量少。副矿物主要是磁铁矿、石榴石、榍石和锆石。交代结构发育,蚀变现象普遍。主要化学组分和微量元素含量及δ18O值变化范围大。该二长岩体是由老片麻岩经热液碱交代作用而成。     

Water-saturated and undersaturated melting relations in a Paricutin andesite and an estimate of water content in the natural magma

Phase relations have been determined for a Paricutin Volcano andesite at pressures to 10 kilobars and for H₂O contents in the melt of 2 to 10 weight percent. Runs were made under H₂O-saturated and undersaturated conditions. In undersaturated runs a H₂O-CO₂ fluid phase was always present. Fugacity of H₂O in melt, which is directly related to H₂O content in the melt, was calculated from thermodynamic data. Plagioclase was found to be the liquidus phase when H₂O contents in melt were less than about two percent. With more H₂O, orthopyroxene, in some cases joined by olivine, assumes the liquidus. Clinopyroxene crystallizes near the liquidus only for H₂O contents greater than five percent. The upper temperature stability limit of hornblende is about 950° C, well below the other silicate liquidi except at H₂O-saturated conditions above 5 kb.The geometry of undersaturated liquidi and experimental phase compositions may be compared to the mode and phase compositions of the natural rock. From this comparison, megaphenocrysts of the natural rock are interpreted to have crystallized from a lava which had a water content of 2.2±0.5 percent and a temperature of 1110±40°C. Mass-balance calculations on experimental and natural phase assemblages show that the Paricutin series could not have formed by fractionation at pressures less than 10 kb; rather, it was probably derived by partial melting of subducted basaltic oceanic floor.     

Fracture-zone conditions on a recently active fault: insights from mineralogical and geochemical analyses of the Hirabayashi NIED drill core on the Nojima fault, southwest Japan, which ruptured in the 1995 Kobe earthquake

An 1800-m-deep borehole into the Nojima fault zone was drilled at Nojima-Hirabayashi, Japan, after the 1995 Hyogo-ken Nanbu (Kobe) earthquake. Three possible fracture zones were detected at depths of about 1140, 1300, and 1800 m. To assess these fracture zones in this recently active fault, we analyzed the distributions of fault rocks, minerals, and chemical elements in these zones. The central fault plane in the shallowest fracture zone was identified by foliated blue-gray gouge at a depth of 1140 m. The degree of fracturing was evidently greater in the hanging wall than in the footwall. Minerals detected in this zone were quartz, orthoclase, plagioclase, and biotite, as in the parent rock (granodiorite), and also kaolinite, smectite, laumontite, stilbite, calcite, ankerite, and siderite, which are related to hydrothermal alteration. Biotite was absent in both the hanging wall and footwall across the central fault plane, but it was absent over a greater distance from the central fault plane in the hanging wall than in the footwall. Major element compositions across this zone suggested that hydrothermal alteration minerals such as kaolinite and smectite occurred across the central fault plane for a greater distance in the hanging wall than in the footwall. Similarly, H₂O+ and CO₂ had higher concentrations in the hanging wall than in the footwall. This asymmetrical distribution pattern is probably due to the greater degree of wall–rock fracturing and associated alteration in the hanging wall. We attributed the characteristics of this zone to fault activity and fluid–rock interactions. We analyzed the other fracture zones along this fault in the same way. In the fracture zone at about 1300 m depth, we detected the same kinds of hydrothermal alteration minerals as in the shallower zone, but they were in fewer samples. We detected relatively little H₂O+ and CO₂, and little evidence for movement of the major chemical elements, indicating little past fluid–rock interaction. In the fracture zone at about 1800 m depth, H₂O+ and CO₂ were very enriched throughout the interval, as in the fracture zone at about 1140 m depth. However, smectite was absent and chlorite was present, indicating the occurrence of chloritization, which requires a temperature of more than 200 °C. Only smectite can form under the present conditions in these fracture zones. The chloritization probably occurred in the past when the fracture zone was deeper than it is now. These observations suggest that among the three fracture zones, that at about 1140 m depth was the most activated at the time of the 1995 Hyogo-ken Nanbu (Kobe) earthquake.     

A FORTRAN Program for tabulating and naming amphibole analyses according to the International Mineralogical Association Scheme

Summary Amphibole analyses input to program AMPHTAB (optionally with H₂O, F, Cl, minor elements and one or both of Fe₂O₃, FeO), are output in conventional column tables, with formula units, complete IMA names, and extensive messages indicating the quality of each analysis. AMPHTAB accepts data-files ranging from a single amphibole analysis to (in principle) unlimited batched data-e.g., multiple analyses from each of numerous probe sections. Options are provided to reallocate total Fe in probe data between Fe³ and Fe², to allow for common analytical problems (e.g., low H₂O values), and to enable the number of oxygens in the formula unit to be either preset or assigned automatically. Results for 57 probe analyses are compared with an unpublished BASIC program, which uses a different Fe-reallocation method. Three-quarters of the IMA names resulting from the two programs are essentially identical, despite somewhat different estimated formula units. The remainder are borderline cases, where incidental changes in formula units effect disproportionate differences in name.

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Ein FORTRAN-Programm zum tabellieren und benennen von amphibolanalysen entsprechend dem Schema der International Mineralogical Association

Zusammenfassung In das Programm eingegebene Amphibolanalysen (wahlweise mit H₂O, F, Cl, Spurenelementen und Fe₂O₃, und/oder FeO), werden in Form herkömmlicher Spaltentabellen mit den Formeleinheiten, vollständigen IMA-Namen und ausführlichen Bemerkungen bezüglich der Analysenqualität ausgegeben. Das AMPHTAB-Programm verarbeitet Datensätze von einer einzigen Amphibolanalyse bis zu (im Prinzip) unbegrenzten Datenblöcken; z. B. Mehrfachanalysen eines Probenabschnittes von mehreren. Es sind die Möglichkeiten vorgesehen, das Gesamteisen in einer Analyse in die Fe³ und Fe²-Anteile umzurechnen, allgemeine analytische Probleme (z. B. niedrige H₂O-Gehalte) zu lösen und die Anzahl der Sauerstoffatome in der Formeleinheit entweder vorzugeben oder automatisch setzen zu lassen. Die Resultate von 57 Mikrosonden-Analysen sind mit einem unveröffentlichten BASICProgramm, das eine andere Methode zur Aufteilung des Fe-Gehaltes benutzt, verglichen worden. Drei Viertel der von den beiden Programmen vorgeschlagenen Mineralnamen sind identisch, trotz einiger unterschiedlich berechneter Formeleinheiten. Die übrigen 25% sind Grenzfälle, bei denen zufällige Veränderungen in den Formeleinheiten unverhältnismäßige Unterschiede in der Benennung bewirkten.