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1.
In this contribution we report a study of poorly exposed, rhyodacitic welded-ignimbrite deposit from Minas Gerais. A petrographic study of textures indicate high temperature of emplacement. Key features include eutaxitic texture, flattened and agglutinated lapilli and glass menisci. Most of the feldspar minerals and glass are extensively altered to clay minerals, which pseudomorph the original volcanic textures. Glass menisci and spherules suggest a possible process of liquid immiscibility. Immobile trace element distribution indicates a possible link with other post-Palaeozoic felsic volcanic rocks in Brazil, a magmatism interpreted as due to basaltic underplating and partial melting of a hydrous continental crust. A peculiar feature is a high Light REE/Heavy REE ratio. Depletion in heavy rare earth elements is possibly due to a residual HREE-bearing phase in the source. The geologic context of these rocks suggests a Lower Cretaceous age and a tectonic relationship with a continental rifting event. 相似文献
2.
Mainly high-K, calc-alkaline, Late Miocene to Pliocene volcanic rocks cropped out of the Konya area in Central Anatolia, Turkey. The volcanic rocks are predominantly andesitic to dacitic in composition and rarely basalt, basaltic andesite, basaltic trachyandesite and pyroclastics. Kaolinite, illite, Ca-montmorillonite, alunite, jarosite, minamiite and silica polymorphs were formed by widespread and intense hydrothermal alteration in or around the volcanic products. To investigate the effects of hydrothermal alteration on the chemistry of volcanic rocks, the whole rock chemical composition (major and trace elements, including rare-earth elements (REE) was analysed. The results of the study demonstrate notable differences in the REE behaviour in the different sample groups. REE trends of fresh parent rocks to weakly-, moderately-altered, kaolinitic and alunitic rocks are characterised by strong LREE enrichment ((La/Lu)cn = 14.57, 11,8 to 15.20, 4.54 to 13.30, 12.5 to 24.2 and 34.6 to 47.26, respectively). Most of the samples have pronounced negative and/or weakly-negative Eu anomalies ranging from 0.75 to 0.98 while three samples have weakly-positive Eu anomalies. LRE element contents are higher than those of HREE in the samples. The LRE elements were strongly enriched in the kaolinitic and alunitic alteration; in weakly- and moderately-altered rocks. LREE are nearly immobile whereas HRE elements show different behaviour in different rock groups. The HFS and TRT elements are slightly mobilised in weakly-altered rocks, but enriched in other alteration types. Elements commonly assumed to be immobile (e.g. Y, Zr, Nb, Hf, TiO2, Al2O3, REE) show variation in mass calculation. LIL elements showed enrichment over LREE and MREE, and similar behaviour, in contrast with HFSE. A clear increment of trans-transition elements (TRTE) was found mainly in alunitic and partly in kaolinitic samples. 相似文献
3.
Séverine Moune Pierre-J. Gauthier Olgeir Sigmarsson 《Geochimica et cosmochimica acta》2006,70(2):461-479
During its last eruption in February 2000, Hekla volcano (Iceland) emitted a sub-Plinian plume that was condensed and scavenged down to the ground by heavy snowstorms, offering the unique opportunity to study the chemistry of the gaseous plume released during highly explosive eruptions. In this paper, we present results on trace element and minor volatile species (sulfates, chlorides, and fluorides) concentrations in snow samples collected shortly after the beginning of the eruption. The goal of this study is to better constrain the degassing and mobility of trace elements in gaseous emissions. Trace element volatility at Hekla is quantified by means of enrichment factors (EF) relative to Be. Well-known volatile trace elements (e.g., transition metals, heavy metals, and metalloids) are considerably enriched in the volcanic plume of Hekla. Their abundances are governed by the primary magmatic degassing of sulfate and/or halide compounds, which are gaseous at magmatic temperature. Their volatility is, however, slightly lower than in basaltic systems, most likely because of the lower magma temperature and higher magma viscosity at Hekla. More surprisingly, refractory elements (e.g., REE, Th, Ba, and Y) are also significantly enriched in the eruptive plume of Hekla where their apparent volatility is two orders of magnitude higher than in mafic systems. In addition, REE patterns normalized to the Hekla 2000 lava composition show a significant enrichment of HREE over LREE, suggesting the presence of REE fluorides in the volcanic plume. Such enrichments in the most refractory elements and REE fractionation are difficult to reconcile with primary degassing processes, since REE fluorides are not gaseous at magma temperature. REE enrichments at Hekla could be attributed to incongruent dissolution of tephra grains at low temperature by F-rich volcanic gases and aerosols within the eruptive plume. This view is supported by both leaching experiments performed on Hekla tephra and thermodynamic considerations on REE mobility in hydrothermal fluids and modeling of glass dissolution in F-rich aqueous solutions. Tephra dissolution may also explain the observed enrichments in other refractory elements (e.g., Th, Y, and Ba) and could contribute to the degassing mass balance of some volatile trace elements, provided they are mobile in F-rich fluids. It thus appears that both primary magmatic degassing and secondary tephra dissolution processes govern the chemistry of eruptive plumes released during explosive eruptions. 相似文献
4.
Distribution of the rare-earth elements (REE) in dacite has been studied so as to get a better understanding of the migration
behavior of REE during alteration. Both unaltered and altered samples were collected in an unpolluted area of Guangxi Zhuang
Autonomous Region, southwest China. The REE concentrations were analyzed by ICP-MS. It is concluded that the REE were enriched
during dacite alteration in varying degrees. The chondrite-normalized REE patterns of altered samples approximately maintain
the characteristics of unaltered samples. However, if we normalize the REE concentrations of altered samples with unaltered
dacite, fractionation of REE will appear. The LREE are more enriched than HREE in all altered samples with the LREE possibly
precipitated as carbonate minerals. Both positive and negative Eu anomalies exist. Enrichment, immobility and depletion are
noticed for the element Lu. Heavy mineral alteration, difference in stability constant between carbonate LREE and HREE complexes,
downward migration of weathering fluid and microenvironment change may be responsible for the fractionation of REE in the
altered dacite. 相似文献
5.
Shilpa Vuba Sadia Farnaaz Netramani Sagar S. Masood Ahmad 《Journal of the Geological Society of India》2013,82(3):217-226
The major, trace and rare earth elements geochemistry and clay mineral compositions in the river bed sediments from lower reaches of Godavari river suggest that they are derived from weathering of felsic rocks. Trace and rare earth elemental compositions indicate evidence of sedimentary sorting during transportation and deposition. Lower concentrations of transition elements, such as V, Ni and Cr imply enrichment of felsic minerals in these bed sediments. The REE pattern in lower Godavari sediments is influenced by the degree of source rock weathering. The light rare earth elements (LREE) content are indicating greater fractionation compared to the heavy rare earth elements (HREE). A striking relationship is observed between TiO2 and gZREE content suggesting a strong control by LREE-enriched titaniferous minerals on REE chemistry. Shale-normalized REE pattern demonstrate a positive Eu anomaly, suggesting weathering of feldspar and their secondary products, which are enriched in Eu. Chondrite-normalised REE pattern is characteristic of felsic volcanic, granites and gnessic source rocks. Trace elemental compositions in sediments located near urban areas suggest influence of anthropogenic activity. Chemical Index of Alteration (CIA) is high (avg. 65.76), suggesting a moderate chemical weathering environment. X-ray diffraction analysis of clay fraction shows predominance of clay minerals that are formed because of the chemical weathering of felsic rocks. 相似文献
6.
The Upper Red Formation (URF) comprises over 1–5 km of late Miocene siliciclastic sediments in the Central Iran Basin. The formation is dominated by volcaniclastic conglomerates and arenites. The prevailing arid conditions during most of the basin's history resulted in deposition of predominantly organic‐poor, red sediments with gypsum and zeolites. This investigation concentrates on the mineralogy and geochemistry of the URF in the southern and northern margins of the basin where the formation was buried to depths of 2.4 and 6.6 km, respectively. Fine fraction mineral separates from the southern margin consist of nearly pure smectite and zeolites at a depth of 400 m and smectite with minor quartz and calcite at 1800 m. Shallow samples (1350 m) from the northern section are rich in smectite, illite/smectite with some discrete illite and chlorite. This assemblage is progressively replaced by discrete illite and chlorite with increasing burial depth so that only these two minerals are found at depths greater than 4300 m. The initial alteration process involved replacement of glass and volcanic lithics by smectite and zeolites in both margins of the basin. Increased depth of burial in the northern margin resulted in the progressive isochemical alteration of smectite to discrete illite and chlorite. Diagenesis of clay assemblages occurred essentially in a closed system. Solute products of glass hydrolysis reactions were retained in highly alkaline, saline ground waters from which zeolites, carbonates and oxides precipitated as cements. It is unlikely that these sediments were ever significantly leached by meteoric waters or by organic acids generated during burial diagenesis. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
7.
Anne Salaün Benoît Villemant Martine Gérard Jean-Christophe Komorowski Agnès Michel 《Journal of Geochemical Exploration》2011,111(3):59-83
The mineralogy and the trace element compositions of hydrothermally-altered volcanic materials collected from ash fall deposits and in four debris-avalanche deposits (DADs) at La Soufrière volcano in Guadeloupe have been determined. Phreatic explosions of the 1976 eruption and flank collapse events have sampled various parts of the active and ancient hydrothermal systems of the volcano. Hydrothermal mineral assemblages (smectite + silica polymorphs ± pyrite/jarosite ± gypsum) are typical of rock alteration by low-temperature acid-sulphate fluids. High-temperature mineral assemblages are rare, indicating that phreatic explosions and flank collapse events have sampled mainly the upper parts of the volcanic edifice.Andesitic eruptive products affected by shallow hydrothermal alteration are complex assemblages of volcanic materials (glass, phenocrysts and xenocrysts with complex magmatic histories) of different ages and compositions. The use of incompatible element ratios and REE compositions normalised to an unaltered reference material overcomes the interpretation difficulties related to mass balance effects of alteration processes and the petrologic heterogeneity of the initial material.REE and other incompatible elements (Th, U, Hf, Zr) are mainly concentrated in the glassy matrix of unaltered andesitic rocks. Secondary S-bearing mineral phases (e.g., gypsum, jarosite) that have precipitated from acid-sulphate fluids do not contain substantial incompatible elements (REE, U, Th, Hf, Zr). Compositional variations of incompatible elements in hydrothermally-altered andesitic materials reflect mainly volcanic glass–smectite transformation, which is characterised by (i) strong depletion of alkalis and alkaline earths (Ba, Sr) and first transition series elements (Zn, Cu, Cr, Co, Ni), (ii) immobility of highly incompatible elements (Th, Zr, Hf, LREE) and (iii) strong depletion of MREE and HREE. The sigmoid shape of normalised REE pattern is characteristic of glass–smectite transformation by low-temperature acid-sulphate fluids. This transformation also produces significant variations in U/Th values, which offer the opportunity to date the cessation of hydrothermal alteration and to reconstruct the evolution in space and time of hydrothermal activity in a volcanic edifice. 相似文献
8.
《Chemie der Erde / Geochemistry》2019,79(2):235-246
This research is focused on the composition of the sediments produced in volcanic islands when the climate does not favour weathering. The XRD mineralogy (bulk sample and fraction finer than 63 μm), petrography and geochemistry of a set of bedload stream and beach samples collected in the “old” Maio and the “young” Fogo islands of Cape Verde archipelago are used to investigate the compositional transformations promoted by exogenous processes during island denudation. The main factor responsible for the variability in sediment composition is the incorporation of biogenic material derived from the evolving shelves; it largely exceeds the effects of the exhumation of different volcanic and basement units. Given the arid climate (and steep land surface in Fogo), only the most labile components of basaltic rocks, such as volcanic glass, are decomposed. The incipient weathering and sorting processes are responsible for the depletion of Al in bedload deposits. The same happens with other elements usually regarded as non-mobile (namely, Nb, Th, REE, etc.), while Mg is concentrated. Thus, weathering indices grounded on the premise that “mobile” elements are lost and “non-mobile” elements are enriched via weathering are useless in Cape Verde bedload sediments. With time, weathering is able to promote Na leaching and the formation of secondary minerals, which tend to retain non-mobile elements released in the earlier stages of alteration (e.g., LREE, Th, Y, Nb, Ta etc.). Sorting processes are responsible for the selective removal of less-dense grains, explaining local differences between beach and stream deposits. Beach placers are enriched in augitic clinopyroxene (occasionally also in olivine in the Fogo island), and Sc, Cr and Co. Niobium and Ta must be hosted in fine-grained particles that are easily windblown and their abundances in dusts may reveal Cape Verde as a source of airborne material crossing the Atlantic Ocean. 相似文献
9.
本文对嫩江地区中生代双峰式火山岩进行了锆石LA-ICP-MSU-Pb年代学和岩石地球化学研究。测年结果显示嫩江地区中生代双峰式火山岩形成于127.5Ma的早白垩世晚期。岩石地球化学研究表明,早白垩世晚期火山岩具有双峰式组合特点,基性端员富碱,富含轻稀土元素和大离子亲石元素,亏损重稀土元素和高场强元素（Nb、Ta、Ti、Y）,形成于富集的岩石圈地幔的部分熔融和分离结晶作用,形成的过程可能含有少量的陆壳混染。酸性端员显示A型流纹岩的特征,为幔源岩浆底侵,使中下地壳岩石发生部分熔融的成因。双峰式火山岩组合的存在暗示其形成于陆内拉张的构造环境。结合区域上中生代火山岩的空间展布特征,嫩江地区早白垩世晚期双峰式火山岩的形成应与太平洋板块向欧亚大陆的俯冲作用有关。 相似文献
10.
We have analyzed 25 trace elements (e.g., Sb, Tl, Sn, rare earth elements (REE), Th, U, Nb, Pb, Zr, Hf, and Y) in altered mid-ocean ridge basalts (MORB) from locations near the mouth of the Gulf of California. Our results imply that the heavy REE and Y are not seriously affected by seawater alteration, in agreement with previous studies. The elements Zr, Hf, Nb, light REE and Sr are enriched up to a factor of 2 in some extremely altered samples. However, element ratios between Zr, Hf, and Nb (e.g., Zr/Hf, and Zr/Nb) are not greatly affected, presumably due to the chemical similarity of these elements during any exchange process. The enrichment of Th and Sn is even higher. Antimony, Tl, Cs, Rb, Rb, and Ba are most easily altered by water-rock interaction and are therefore the best indicators for seawater alteration. The enrichment factor of the most mobile element Sb is up to 2000.
There is a weak correlation between the concentration in seawater and the enrichment factors. On the other hand, the worldwide pelagic clay pattern matches the enrichment pattern much more closely, and the limited data available for local oceanic sediments give an even better correlation. A plausible model to explain the enrichment pattern may be an elemental exchange between basalt and seawater that had interacted earlier with overlying sediments. 相似文献
11.
义县盆地早白垩世义县组为一套火山-沉积岩系,沉积层中多含凝灰质成分。为了解沉积期火山活动对沉积层产生的影响,对砖城子层火山碎屑泥灰岩(火山事件层)和纹层状泥灰岩夹层、大康堡层纹层状泥灰岩进行岩石学和地球化学的研究。研究表明:火山事件层中含大量的火山碎屑(20%±),其他各层均含凝灰质成份。样品中主量元素Ca O、Mg O和Si O_2含量较高,Si O_2含量变化较大,Al_2O_3含量较低;微量元素与上地壳(UCC)元素比值多小于1,大多数微量元素(Rb、Th、Nb、REE等)处于亏损状态,火山事件层富集Li、Sc、As、Sr和Ag元素。沉积期火山活动对沉积层中Si O_2和K_2O含量影响较大,并可能导致As元素富集。火山事件层样品化学风化指数(CIW)在82~91之间,呈逐渐增加的趋势,指示风化作用强烈。 相似文献
12.
J. J. Cochemé A. C. Lassauvagerie J. Gonzalez-Sandoval E. Perez-Segura P. Münch 《Mineralium Deposita》1996,31(6):482-491
In NW Mexico, zeolite deposits of potential economic interest occur in continental sediments related to mid-Tertiary basin and range tectonism. In central Sonora, where the stratigraphic column is thicker (e.g. in the Moctezuma Basin), two superposed sequences of sediments are distinguished on the basis of their lithology and stratigraphy. They are known as the Baucarit Formation. The lower sequence, Miocene in age and 300 to 400 m thick, is indurated and consists mainly of sandstones and conglomerates. The upper one, of variable thickness, consists of clays. Zeolites occur in both sequences as alteration products of volcanic glass in beds of white intercalated rhyolitic tuff. Previously known outcrops of zeolitites from Rio Batepito (erionite), Tetuachi and San Pedro Ures (heulandite group), Divisaderos (chabazite) and several other newly discovered occurrences are described in this work in terms of mineral association, physical properties (porosity, thermal behaviour) and chemical characteristics (major and trace elements for individual crystals and bulk rock). Heulandite-group minerals are also present as cement (30% by volume) of the sandstones from the lower sequence. Amygdales and veins from basaltic flows intercalated within the lowest sediments contain a large variety of zeolite species: chabazite, stilbite, phillipsite, mesolite, erionite, thomsonite, heulandite and analcime. Zeolites in the pyroclastic beds intercalated in the upper sequence represent the highest economic potential because they are essentially monomineralic and constitute up to 80% in volume of the whole rock. Because of the inhomogeneous distribution of amygdales, zeolites in the basaltic flows have a low economic interest. 相似文献
13.
Michael R. Perfit Hannes Brueckner James R. Lawrence Robert W. Kay 《Contributions to Mineralogy and Petrology》1980,73(1):69-87
Trace elements, including rare earth elements (REE), exhibit systematic variations in plutonic rocks from the Captains Bay pluton which is zoned from a narrow gabbroic rim to a core of quartz monzodiorite and granodiorite. The chemical variations parallel those in the associated Aleutian calcalkaline volcanic suite. Concentrations of Rb, Y, Zr and Ba increase as Sr and Ti decrease with progressive differentiation. Intermediate plutonic rocks are slightly enriched in light REE (La/Yb=3.45–9.22), and show increasing light REE fractionation and negative Eu anomalies (Eu/Eu*=1.03–0.584). Two border-zone gabbros have similar REE patterns but are relatively depleted in total REE and have positive Eu anomalies; indicative of their cumulate nature. Initial 87Sr/86Sr ratios in 8 samples (0.70299 to 0.70377) are comparable to those of volcanic rocks throughout the arc and suggest a mantle source for the magmas. Oxygen isotopic ratios indicate that many of the intermediate plutonic rocks have undergone oxygen isotopic exchange with large volumes of meteoric water during the late stages of crystallization; however no trace element or Sr isotopic alteration is evident.Major and trace element variations are consistent with a model of inward fractional crystallization of a parental high-alumina basaltic magma at low pressures (6 kb). Least-squares approximations and trace element fractionation calculations suggest that differentiation in the plutonic suite was initially controlled by the removal of calcic plagioclase, lesser pyroxene, olivine and Fe-Ti oxides but that with increasing differentiation and water fugacity the removal of sub-equal amounts of sodic plagioclase and hornblende with lesser Fe-Ti oxides effectively drove residual liquids toward dacitic compositions. Major and trace element compositions of aplites which intrude the pluton are not adequately explained by fractional crystallization. They may represent partial melts derived from the island arc crust. Similarities in Sr isotopes, chemical compositions and differentiation trends between the plutonic series and some Aleutian volcanic suites indicates that shallow-level fractional crystallization is a viable mechanism for generating the Aleutian calcalkaline rock series.LDGO Contribution no. 2964 相似文献
14.
A.E. Kelepertsis 《地学学报》1993,5(1):52-60
The mobilities of major and trace elements have been investigated in hydrothermally altered volcanic rocks of Pliocene age on the island of Lesvos. One type of hydrothermal assemblage, montmorillonite-K-feldspar-goethite, was recognized in outcrops north of Mytilini town. The alteration occurs a few metres under the surface of unaltered volcanic rocks of high-K andesite and high-K basaltic andesite composition. The unaltered latite-andesite consists of plagioclase, clinopyroxene, sanidine and magnetite with quartz, calcite, pumpellyite and montmorillonite as subordinate secondary minerals. The main control over major oxide distribution appears to be the extent of conversion of plagioclase to K-feldspar. Three distinct groups of elements were revealed to be positively correlated:
- 1 Si, Mg, Ca, Na, Mn, Sr and Ba, which are leached during the alteration process. This group of elements reflects their association with plagioclase feldspar and clinopyroxene.
- 2 Fe, K, Ti, P, Nb, Zr, Y, Rb, Ni, Cr, V. This group includes elements which are enriched relative to the unaltered volcanic rock, reflecting their association with K-feldspar, iron hydroxides and Ti and P-bearing minerals.
- 3 Ti, P, Nd, La, Ce. From this group of elements it is indicated that Nd, La and Ce are associated with Ti- and P-bearing minerals.
15.
Robert C. Walter William K. Hart John A. Westgate 《Contributions to Mineralogy and Petrology》1987,95(4):462-480
The Cindery Tuff is an unusual tephra fall deposit that contains evidence for the mixing of basaltic and rhyolitic liquids prior to eruption. It contains clear rhyolitic glass shards together with brown basaltic glass spheres and a broadly bimodal phenocryst assemblage. Brown glasses are ferrobasaltic in composition and are similar to the voluminous Pliocene tholeiites of the surrounding west-central Afar volcanic field; both are enriched in the light rare earth and incompatible elements and possess higher 87Sr/86Sr and lower 143Nd/144Nd than MORB. Rhyolitic glasses are subalkaline and, compared to the basaltic glasses, are strongly depleted in the compatible elements and enriched in the incompatible elements. Both glass types have similar incompatible element and isotopic ratios, and with the rhyolite glass showing a 2-fold parallel enrichment in rare earth element abundances over the basaltic glass. These observations suggest that the two glasses are genetically related.Rare glasses with intermediate compositions occur as phenocryst melt inclusions, as mantles on phenocrysts and as free pumice clasts. Their major element contents do not point to an origin by simple hybrid mixing of the basaltic and rhyolitic melts. Rather, major element mixing calculations indicate formation of the intermediate and rhyolite melts by fractionation of the observed phenocryst assemblage, using a starting composition of the observed basaltic glass. Model calculations from trace element data, though lacking from the intermediate glasses, support fractional crystallization. The bimodal mineral assemblage argues against an immiscible liquid origin for the contrasting glass compositions. 相似文献
16.
Rare earth element (REE) patterns of hydrothermally altered rhyolite from geothermal systems located in the Taupo Volcanic Zone in the North Island of New Zealand provide evidence of REE mobility. REE trends of unaltered rhyolites are characterised by moderate LREE enrichment ((La/Lu)cn = 3.84 to 5.62) and pronounced negative Eu anomalies. In contrast, REE patterns of hydrothermally altered rhyolites commonly exhibit different signatures and may be placed into four chemically and petrographically distinct categories. Rocks with clay + quartz + feldspar + calcite (±zeolites, epidote, sphene, chlorite, opaque minerals) assemblages typically display patterns subparallel to fresh rock, whereas, samples which contain quartz + chlorite, or quartz + clay + zeolite assemblages have flat patterns without Eu anomalies, and highly silicified samples are characterised by depleted, bowed REE trends. These patterns may be produced by interaction with alkaline or acid fluids. A fourth group of very intensely altered samples, affected by interaction with acid fluids, exhibits unusual REE trends with highly enriched HREE and depleted LREE, or depleted HREE.These results indicate that some of the REE released by the breakdown of primary phases during alteration are transported away in the fluid. In addition, the degree of depletion is positively correlated with alteration intensity and the fluid/rock ratio. The similarity of REE patterns resulting from alteration by alkaline and acid fluids suggests that the shape of the REE trends is controlled principally by fluid/rock ratios and secondarily by mineralogy. The REE are retained in rocks with a diverse alteration mineralogy, whereas in samples with only one dominant alteration phase (e.g. quartz) it is more probable that not all REE liberated during alteration can be accommodated in the altered rock. Eu commonly behaves differently from the other REE, possibly due to the dominance of Eu2+. 相似文献
17.
目前对于粘土层中伊蒙混层矿物的堆垛结构、单元层含量与岩浆母质及环境条件关系的了解等,仍然十分匮乏.一定沉积环境下火山灰层中粘土矿物组合、以及伊蒙混层堆垛方式精细结构特征,可能记录了沉积(包括成岩作用) 环境对火山物质蚀变产物的影响.采用X射线衍射(XRD)、扫描电子显微镜(SEM)、元素地球化学分析、氧同位素分析方法等方法,对贵州新民深海相二叠系-三叠系(P-T) 界线附近蚀变火山灰层的地球化学特征、粘土矿物精细结构特征等进行了深入研究.结果表明,4个火山灰粘土层均含有2种具有R3结构、不同混层比的伊蒙混层矿物相,且均出现粘土矿物集合体取代原先的火山碎屑颗粒或在颗粒表面生长的现象,粘土矿物形成于沉积-成岩阶段因而其泥质结构被保留;样品XM-5-1和XM-5-2的Fe3+原子数分别为0.16和0.17个且具有明显Eu负异常和较低的K2O含量,而XM-5-3和XM-5-4的Fe3+原子数均为0.14个,说明相对于前2个粘土层,后2个的岩浆母质更加偏向酸性而表现为成岩蚀变程度更强.粘土矿物的氧同位素组成为17.3‰~18.1‰,与常温下蒙脱石与海水的平衡数值相近,表明粘土矿物化学组成与海底成岩蚀变环境有关,而不同火山灰层的粘土矿物学特征则主要取决于岩浆岩母质以及成岩蚀变强度. 相似文献
18.
Abstract: The Onsen acid‐sulphate type of mineralization is located in the Desmos caldera, Manus back‐arc basin. Hydrothermal precipitates, fresh and altered basaltic andesite collected from the Desmos caldera were studied to determine mineralization and mobility of elements under seawater dominated condition of hydrothermal alteration. The mineralization is characterized by three stages of advanced argillic alteration. Alteration stage I is characterized by coarse subhedral pyrophyllite with disseminated anhedral pyrite and enargite which were formed in the temperature range of 260–340°C. Alteration stage II which overprinted alteration stage I was formed in the temperature range of 270–310°C and is characterized by euhedral pyrite, quartz, natroalunite, cristobalite and mixed layer minerals of smectite and mica with 14–15 Å XRD peak. Alteration stage III is characterized by amorphous silica, native sulphur, covellite, marcasite and euhedral pyrite, which has overprinted alteration stages I and II. Relative to the fresh basaltic andesite samples, the rims and cores of the partly altered basaltic andesite samples have very low major, minor and rare earth elements content except for SiO2 which is much higher (58–78 wt%) than SiO2 content of the fresh basaltic andesite (55 wt%). REE patterns of the partly altered basaltic andesite specimens are variably depleted in LREE and have pronounced negative Eu anomalies. Normalization of major, minor and REE content of the partly altered basaltic andesites to the fresh basaltic andesite indicates that all the elements except for SiO2 in the partly altered basaltic andesite are strongly lost (e.g. Al2O3 = ‐8.3 to ‐10.9 g/100cm3, Ba = ‐2.2 to ‐5.6 mg/100cm3, La = ‐130 to ‐200 μg/100cm3) during the alteration process. Abnormal depletion of MgO, total Fe as Fe2O3, LREE especially Eu and enrichment of SiO2 in the altered basaltic andesites from the Desmos caldera seafloor is caused by interaction of hot acidic hydrothermal fluid, which originates from a mixing of magmatic fluid and seawater. 相似文献
19.
Ulrike Wirsching 《Contributions to Mineralogy and Petrology》1975,49(2):117-124
In the formation of zeolites by hydrothermal alteration volcanic glasses are the starting material in most cases. The experiments aimed at demonstrating in what way the chemistry of the volcanic glass influences:
- the alteration rate of the volcanic glass to zeolites,
- the kind of zeolites being formed and their formation conditions.
20.
西天山阿希金矿成矿地球化学特征研究 总被引：11，自引：0，他引：11
阿希金矿为1990年代在西天山发现的产于晚古生代陆相火山岩中的大型金矿床.容矿围岩为下石炭统大哈拉军山组中基性-中酸性火山岩,以钙碱性为主,少量碱性系列岩石,具有富硅、钠,贫铝、钾、镁、钙成分和里特曼指数偏高的特点;岩石稀土元素含量中等,属于轻稀土富集型,分馏程度较高;容矿火山岩以K、Rb、Ba、Th等大离子元素富集和Ti、Y、Yb、Sc等亏损为特征,接近于板内过渡型玄武岩系列岩石;容矿岩、近矿蚀变岩和矿石皆富集有Au、Ag、As、Sb、Bi等低温组合元素,且表现出渐进富集之特点;火山岩和矿石中铅具壳幔混合源特征;含金石英脉锶同位素初始值与区内容矿火山岩、矿化有关的蚀变矿物十分接近,均小于0.709而大于0.705;成矿流体属于K+[Na+]-SO42-[Cl-]型,具有低温(120~180℃)、低压(7.2~21.8 MPa)、低盐度(2.4%~4.5%,NaCl)、富含CO2、N2、O2等特征;流体pH值中等(5.7~8.8),Eh值-0.88~+1.18 eV,成矿环境弱还原;金矿石中黄铁矿δ34S值0.95‰~10.51‰,以深源火山成因硫为主;氢氧同位素值域较宽,反映流体以大气降水为主.总之,阿希金矿具备了浅成低温热液系统金矿的基本地球化学特征,但在成矿时代和成矿背景等方面,有别于经典同类矿床. 相似文献