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1.
Variations in the abundances of Zn, Cu, and Pb are found to be useful in identifying tectonic regimes and separating oceanisland basalts into enriched- and depleted-source categories. The average Zn, Cu, and Pb contents of normal mid-ocean ridge basalts (N-MORB) are 84, 70, and 0.35 ppm, respectively. Differences in average Zn contents for various ridges reflect more the varying degrees of differentiation than variations of Zn content in the source rocks. At a Mg# of 70, or Mg#70, which is taken to represent primitive MORB, many MORB sequences converge at a Zn content of 58 ± 6 ppm, which is close to the value for primitive mantle (50 ppm) and ordinary chondrites (～55 ppm). Values of 0.1 to 0.15 ppm Pb in MORB at Mg#70, best defined at the superfast-spreading Southern East Pacific Rise, are similar to estimates of Pb in the primitive mantle (0.12 to 0.18 ppm). They also are near the lower end of the range for ordinary chondrites. The very slow spreading Southwest Indian Ocean Ridge has a sequence with higher Pb contents, in addition to a more normal sequence, which has a visual best value of 0.4 ppm Pb at Mg#70. With the exception of the Walvis Ridge, Zn and Cu appear to be little affected by proximity to hotspots (i.e., E-MORB); however, Pb contents are higher and average about 0.6 ppm.

Both Zn and Pb in MORB are incompatible elements (i.e., favor the melt), but Cu is a compatible element. At Mg#70, there is the suggestion of a value of 100 ppm for Cu, with lower values possibly representing partial removal of sulfides and their associated Cu from the source. Nonetheless, Cu contents of primitive MORB tend to be much higher than even high estimates for the primitive mantle (28 ppm), and are closer to ordinary chondrites (～90 ppm). Therefore, Zn, Cu, and Pb all approximate chondritic values in the primitive MORB melt.

Average contents of Zn, Cu, and Pb in oceanic island basalts (OIB) are 115, 62, and 3.2 ppm, respectively. At Mg#70, values of Zn and Cu are similar to the respective averages for OIB, with Zn higher and Cu lower than MORB. At a Mg# of ～40, however, OIB and MORB tend to have similar Zn contents. With further differentiation, OIB trachytes can contain >200 ppm Zn. Unlike MORB, OIB can differentiate to high Cu contents of 200 ppm at Mg#s of 40 to 60. In contrast to Zn and Cu, Pb regresses to a value of 0.83 ppm at Mg#70 for Hawaiian and Reunion volcanics, which is much less than the average value for Pb in OIB volcanics, but higher than for MORB.

Average Zn, Cu, and Pb contents of magmatic-arc basalts are 77, 108, and 1.9 ppm, respectively. In basalts, Zn tends to be incompatible, but a dual incompatible and compatible behavior can occur at high SiO2 contents. Dacites may average near 55 ppm Zn, but peralkalic rhyolite can contain >300 ppm Zn. A dual compatible and incompatible nature occurs for Cu. Most common, particularly in submarine volcanics, is a compatible trend, with a Cu content of around 80 ppm at a Mg# of 60, which decreases to less than 40 ppm at a Mg# of 30. The incompatible trend of increasing Cu can achieve >200 ppm at a Mg# of 30, leaving a gap approaching 100 ppm at that Mg#. The gap is less obvious on a plot of Cu vs. SiO2, but is still there. The compatible trend is proposed to result from sulfur-saturated magmas, whereas the incompatible trend is believed to result from sulfur-deficient magmas. Support for this hypothesis is found in sparse sulfur-isotope data. Zn and Cu both can be incompatible over an extended range of Mg#s or silica content. When Zn and Cu are both compatible, Cu decreases more than twice as rapidly as Zn.

Primitive magmas at Mg#70 average about 50 ppm Zn for submarine Mariana arc basalts and 58 ppm for forearc boninites, contents close to MORB values. Mariana arc basalts have a Zn content of ～45 ppm estimated at Mg#70. Cu varies more widely than Zn in primitive magmas, being about 50 ppm Cu for Mariana Islands volcanics and 120 ppm for Kermadec Islands volcanics, a range broadly around MORB values. Average Pb contents are 1.9 ppm for island-arc tholeiites, 5.6 ppm for high-Al basalt, and 3.2 ppm for alkali basalt with average boninite of approximately 1.8 ppm. Back-arc-basin basalts in the deepest parts of the Mariana trough have Pb contents of 0.45 ppm, but more shallow parts may exceed 1.0 ppm Pb. Although the lower contents are similar to MORB values, the 208Pb/204Pb values are greater than Pacific Ocean MORB. At Mg#70 for rocks from the Tonga and Kermadec island arcs, the Pb content is about 0.1 ppm, similar to MORB.  相似文献   

2.
True graphic quartz structures in pegmatites from Carrara/Giggiga and Harrar (town) districts of Ethiopia, are compared with the micrographic quartz textures in the Rapakiwi granite of Finland. Graphic-like textures of uraninite in microcline are also discussed and compared with these graphic structures.A quartz vein, about 1–2 meters in thickness, intersects a pegmatite in the Carrara/Giggiga district. This quartz vein extends into the microcline of the pegmatite as fine quartz veins which attain the form and character of graphic quartz. Also the graphic quartz of the Harrar pegmatites is observed to extend into and occupy cracks in the microcline.Comparable in origin to these graphic textures is the micrographic quartz in the Rapakiwi granite. Observations show micrographic quartz following the cleavage directions in the orthoclase as well as the interzonal spaces and the boundaries of inclusions in the K-feldspar.On the basis of the observed structures and textures these graphic and micrographic intergrowths are considered to be due to solutions penetrating or infiltrating into existing structures and not due to simultaneous crystallisation as conditions of eutectic crystallisation would require.In addition to the well known graphic structures there occur graphic or myrmekitic-like intergrowths of uraninite in microcline which, from a structural and physico-chemical point of view, cannot be considered to be due to eutectic crystallisation.  相似文献   

3.
Fine atmospheric dust includes mineral particles and aggregates, fibrous minerals and fibrous organic material. Generation, dislodgement and transport （deflation） of natural dust with the finer （〈4 microns） components suspended as silt-size aggregates, is widespread in and adjacent to the world＇s drylands, as well as deriving from volcanic vents. Silica is a highly fibrogenic agent in lung tissue. Long-term inhaling of siliceous dusts can lead to a number of fibrotic lung diseases, including natural （non-occupational） pneumoconioses （notably silicosis, but including asbestosis and others）. Different polymorphs of silica show different levels of toxicity in interaction with lung tissue. Particles with highly active surfaces may release radicals, causing cell damage. Some types of inhaled particulates are degraded by macrophages, but many are highly resistant and persist in the lungs, some stimulating fibroblastic cells to deposit collagen. Silicosis is an inflammation of the lung commonly caused by silicate mineral particles, leading to fibrosis. Three types are recognized： nodular pulmonary fibrosis （simple or chronic silicosis）, acute silicosis, and accelerated silicosis. Generally, finer particulates have greater oxidative capacity than the coarser fractions. They contain more reactive oxygen species, their greater bioreactivity making them more toxic to pulmonary tissue. Nevertheless, inhalation of large dust particles （〉 10μm） may constitute a health risk if the mineralogy is toxic, regardless of where the grains lodge in the respiratory system. Dust may absorb harmful gases, disease-generating bacteria and carcinogenic hydrocarbon compounds. Silica-related respiratory disease may also an exacerbate cardiac problem, and epidemiology suggests a link with tuberculosis. Quantification of dust loading and exposure requires study of spatial and temporal patterns, supported by meteorological analysis, airflow modeling and satellite-borne imagery. Some acute, short-term health impacts have been assessed using atmospheric and health records both before and after a dust storm or by comparison of populations within and outside such events. Analysis of the size, shape, mineralogy and geochemistry of ambient dust particulates provides information on natural dust sources, dust concentrations, and potential particulate toxicity, as well as providing a datum for assessment of human exposure levels.  相似文献   

4.
Asteroid impact spherule layers and tsunami deposits underlying banded iron-formations in the Fortescue and Hamersley Groups have been further investigated to test their potential stratigraphic relationships. This work has included new observations related to the ca 2.63 Ga Jeerinah Impact Layer (JIL) and impact spherules associated with the 4th Shale-Macroband of the Dales Gorge Iron Member (DGS4) of the Brockman Iron Formation. A unit of impact spherules (microkrystite) correlated with the ca 2.63 Ga JIL is observed within a >100 m-thick fragmental-intraclast breccia pile in drill cores near Roy Hill. The sequence represents significant thickening of the impact/tsunami unit relative to the JIL type section at Hesta, as well as relative to the 20–30 m-thick ca 2.63 Ga Carawine Dolomite spherule-bearing mega-breccia. The ca 2.48 Ga-old Dales Gorge Member of the Brockman Iron Formation is underlain by an ?0.5 m-thick rip-up clast breccia located at the top of the ca 2.50 Ga Mt McRae Shale, and is interpreted as a tsunami deposit. We suggest that the presence of impact ejecta and tsunami units stratigraphically beneath a number of banded iron-formations, and units of ferruginous shale in the Pilbara and South Africa may result from a genetic relationship. For example, it could be that under Archean atmospheric conditions, mafic volcanism triggered by large asteroid impacts enriched the oceans in soluble FeO. If so, seasonal microbial and/or photolytic oxidation to ferric oxide could have caused precipitation of Fe2O3 and silica. In view of the possible occurrence of depositional gaps and paraconformities between impact ejecta units and overlying ferruginous sediments, these relationships require further testing by isotopic age studies.  相似文献   

5.
The characteristic structures of the Precambrian cherts from the Gusui section, Guangdong ,Chi-na, include bedded structure ,laminated structure ,massive structure and pseudobrecciated structure.The chert is characterized by consistently low abundance of TiO2,Al2O3 and most trace elements.Howevver ,it is enriched in Ba,As,Sb,Hg and Se.In Al-Fe-Mn ternary diagrams,it falls into the “hydrothermal field“ .Correspondence analysis and factor analysis show that many elements show up in the factor that represents the leaching of country rocks by hydrothermal solutions,and are the very characteristic element association fo the geochemically anomalous South China basement.Petrologic and geochemical evidence suggests a hydrothermal origin for the chert.The chert may have been formed in a Precambrian fift or an extension zone developed within the Yunkai marginal geosyncline, with a fault system linking it to an unknown heat source at depth.  相似文献   

6.
This study is aimed at determining the diffusion coefficient of net-work modifiers (mainly Na, K, and Ca) in a two-phase melt-NaCl system, in which the melts are granitic and the system is NaCl-rich in composition. The diffusion coefficients of Na, K, and Ca were measured at the temperatures of 750 – 1400°C, pressures of 0.001 × 108 – 2 × 108 Pa, and initial H2O contents of 0 wt% –6.9 wt% in the granitic melts. The diffusion coefficients of Fe and Mg were difficult to resolve. In all experiments a NaCl melt was present as well. In the absence of H2O, the diffusion of net-work modifiers follows an Arrhanious equation at 1 × 105 Pa: lgDca=−3. 88−5140/T, lgDk =−3. 79−4040/T, and lgDNa, =−4.99−3350/T, where D is in cm2 /s andT is in K. The diffusion coefficients of Ca, Na, K, and Fe increase non-linearly with increasing H2O content in the melt. The presence of about 2 wt% H2O m the melt will lead to a dramatical increase in diffusivity, but higher H2O content has only a minor effect. This change is probably the result of a change in the melt structure when H2O is present. The diffusion coefficients measured in this study are significantly different from those in previous works. This may be understood in terms of the “transient two-liquid equilibrium” theory. Element interdiffusion depends not only on its concentration, but also on its activity co-efficient gradient, which is reflected by the distribution coefficient, of the two contacting melts.  相似文献   

7.
Epochs of changing atmospheric CO2 and seawater CO2–carbonic acid system chemistry and acidification have occurred during the Phanerozoic at various time scales. On the longer geologic time scale, as sea level rose and fell and continental free board decreased and increased, respectively, the riverine fluxes of Ca, Mg, DIC, and total alkalinity to the coastal ocean varied and helped regulate the C chemistry of seawater, but nevertheless there were major epochs of ocean acidification (OA). On the shorter glacial–interglacial time scale from the Last Glacial Maximum (LGM) to late preindustrial time, riverine fluxes of DIC, total alkalinity, and N and P nutrients increased and along with rising sea level, atmospheric PCO2 and temperature led, among other changes, to a slightly deceasing pH of coastal and open ocean waters, and to increasing net ecosystem calcification and decreasing net heterotrophy in coastal ocean waters. From late preindustrial time to the present and projected into the 21st century, human activities, such as fossil fuel and land-use emissions of CO2 to the atmosphere, increasing application of N and P nutrient subsidies and combustion N to the landscape, and sewage discharges of C, N, P have led, and will continue to lead, to significant modifications of coastal ocean waters. The changes include a rapid decline in pH and carbonate saturation state (modern problem of ocean acidification), a shift toward dissolution of carbonate substrates exceeding production, potentially leading to the “demise” of the coral reefs, reversal of the direction of the sea-to-air flux of CO2 and enhanced biological production and burial of organic C, a small sink of anthropogenic CO2, accompanied by a continuous trend toward increasing autotrophy in coastal waters.  相似文献   

8.
A May 2007 tornado destroyed 95% of aging, declining Greensburg, Kansas. The city took the opportunity to build back “stronger, better, and greener,” enforcing upgraded codes, requiring city-owned buildings to meet LEED Platinum level standards, and recommending energy-efficiency housing in a new Sustainable Comprehensive Plan. Using information collected from surveys of Greensburg tornado survivors, interviews, and publications, we examined the housing-related recovery, including the emergency provision of temporary shelter and rebuilding permanently. Although temporary shelter kept residents nearby for rebuilding, given the gap between insurance policy limits on the aging housing stock and rebuilding costs, housing affordability is a critical issue in Greensburg’s recovery. Local, state, and federal support have made construction of municipal buildings at LEED Platinum level and some affordable and green housing projects possible. However, far greater public and private sector funding for affordable workforce housing, in conjunction with broader economic and job development, is needed.  相似文献   

9.
This article explores the role of geographical context in generating a stigmatised identity among residents of Tara rural subdivisions in the coal seam gas fields in Queensland’s Western Downs. The research was based on qualitative interviews with Tara ‘Blockies’, as these residents are commonly referred to, that revealed how their existence in the middle of an agrarian region resulted in the assignation of a stigma that has marked them as different, and subsequently devalued their status. We explain that this distinction and category division of the normals, referring to Tara’s Agrarian residents, from the ‘stigmatised’ led to an antagonistic relationship that prevented successful socio-cultural assimilation. We demonstrate how an immoral place becomes disadvantaged, resulting in poor well-being, and how imposed labels threaten the self-esteem of its occupants.  相似文献   

10.
We collected groundwaters in and around a large (313 Mt at 1.08% Cu and 0.3% cutoff) undisturbed porphyry copper deposit (Spence) in the hyperarid Atacama Desert of northern Chile, which is buried beneath 30–180 m of Miocene piedmont gravels. Groundwaters within and down-flow of the Spence deposit have elevated Se (up to 800 μg/l), Re (up to 31 μg/l), Mo (up to 475 μg/l) and As (up to 278 μg/l) concentrations compared to up-flow waters (interpreted to represent regional groundwater flow). In contrast, Cu is only elevated (up to 2036 μg/l) in groundwaters recovered from within the deposit; Cu concentrations are low down gradient of the deposit. The differential behavior of the metals/metalloids occurs because the former group dissolves as anions, enhancing their mobility, whereas the base metals dissolve as cations and are lost from solution most likely through adsorption to clay surface exchange sites and through formation of secondary copper chlorides, carbonates, and oxides. Most groundwaters within and down-flow of the deposit have Eh–pH values around the FeII/FeIII phase boundary, limiting the impact of Fe-oxyhydroxides on oxyanions mobility. Se, Re, Mo, and As are all mobile (with filtered/unfiltered samples ～ 1) to the limit of sampling 2 km down gradient from the deposit. The increase in ore-related metals, metalloids, and sulfate and decrease in sulfate–S isotope ratios (from values similar to regional salars, + 4 to + 8‰ δ34SCDT to lower values closer to hypogene sulfides, + 1 to + 4‰ δ34SCDT) is consistent with active water–rock reactions between saline groundwaters and the Spence deposit. It is likely that hypogene and/or supergene sulfides are being oxidized under the present groundwater conditions and mineral saturation calculations suggest that secondary copper minerals (antlerite, atacamite, malachite) may also be actively forming, suggesting that supergene and exotic copper mineralization is possible even under the present hyperarid climate of the Atacama Desert.  相似文献   

11.
A series of coesite,coexisting with or without a liquid phase,was synthesized in the nominal system SiO2-H2O at800-1450℃and 5 GPa.Micro-Raman spectroscopy was used to identity the crystalline phase,electron microprobe and LA-ICP-MS were employed to quantity some major and trace elements,and unpolarized FTIR spectroscopy was applied to probe the different types of hydrogen defects,explore water-incorporation mechanisms and quantify water contents.Trace amounts of A1 and B were detected in the coesite.Combining our results with the results in the literatures,we have found no positive correlation between the Al contents and the"Al"-based hydrogen concentrations,suggesting that previously proposed hydrogen-incorporation mechanism H^++Al^3+■Si^4+does not function in coesite.In contrast,we have confirmed the positive correlation between the B contents and the B-based hydrogen concentrations.The hydrogen-incorporation mechanism H^++B3^+■Si^4+readily takes place in coesite at different P-T conditions,and significantly increases the water content at both liquid-saturated and liquid-undersaturated conditions.For the SiO2-H2O system,we have found that type-Ⅰhydrogarnet substitution plays a dictating role in incorporating water into coesite at liquid-saturated condition,type-II hydrogarnet substitution contributes significantly at nearly dry condition,and both operate at conditions in between.The water solubility of coesite,as dictated by the type-Ⅰhydrogarnet substitution,positively correlates with both P and T,cH2O=-105(30)+5.2(32)×P+0.112(26)×T,with cH2O in wt ppm,P in GPa and T in℃.Due to its low water solubility and small fraction in subducted slabs,coesite may contribute insignificantly to the vertical water transport in subduction zones.Furthermore,the water solubility of any coesite in exhuming ultra-high pressure metamorphic rocks should be virtually zero as coesite becomes metastable.With an adequately fast waterdiffusion rate,this metastable coesite should be completely dry,which may have been the key factor to the partial preservation of most natural Coe.As a byproduct,a new IR experimental protocol for accurate water determination in optically anisotropic nominally anhydrous minerals has been found.Aided with the empirical method of Paterson(1982)it employs multiple unpolarized IR spectra,collected from randomly-orientated mineral grains,to approximate both total integrated absorbance and total integrated molar absorption coefficient.Its success relies on a high-level orientation randomness in the IR analyses.  相似文献   

12.
The paper presents original authors' data on the O, H, C, S, and Sr isotopic composition of water and sediments from the basins into which the Aral Sea split after its catastrophic shoaling: Chernyshev Bay (CB), the basin of the Great Aral in the north, Lake Tshchebas (LT), and Minor Sea (MS). The data indicate that the δ18О, δD, δ13C, and δ34S of the water correlate with the mineralization (S) of the basins (as of 2014): for CB, S = 135.6‰, δ18О = 4.8 ± 0.1‰, δD = 5 ± 2‰, δ13C (dissolved inorganic carbon, DIC) = 3.5 ± 0.1‰, δ34S = 14.5‰; for LT, S = 83.8‰, δ18О = 2.0 ± 0.1‰, δD =–13.5 ± 1.5‰, δ13C = 2.0 ± 0.1‰, δ34S = 14.2‰; and for MS, S = 9.2‰, δ18О =–2.0 ± 0.1‰, δD =–29 ± 1‰, δ13C =–0.5 ± 0.5‰, δ34S = 13.1‰. The oxygen and hydrogen isotopic composition of the groundwaters are similar to those in MS and principally different from the artesian waters fed by atmospheric precipitation. The mineralization, δ13С, and δ34S of the groundwaters broadly vary, reflecting interaction with the host rocks. The average δ13С values of the shell and detrital carbonates sampled at the modern dried off zones of the basins are similar: 0.8 ± 0.8‰ for CB, 0.8 ± 1.4‰ for LT, and –0.4 ± 0.3‰ for MS. The oxygen isotopic composition of the carbonates varies much more broadly, and the average values are as follows: 34.2 ± 0.2‰ for CB, 32.0 ± 2.2‰ for LT, and 28.2 ± 0.9‰ for MS. These values correlate with the δ18O of the water of the corresponding basins. The carbonate cement of the Late Eocene sandstone of the Chengan Formation, which makes up the wave-cut terrace at CB, has anomalously low δ13С up to –38.5‰, suggesting origin near a submarine methane seep. The δ34S of the mirabilite and gypsum (11.0 to 16.6‰) from the bottom sediments and young dried off zone also decrease from CB to MS in response to increasing content of sulfates brought by the Syr-Darya River (δ34S = 9.1 to 9.9‰) and weakening sulfate reduction. The 87Sr/86Sr ratio in the water and carbonates of the Aral basins do not differ, within the analytical error, and is 0.70914 ± 0.00003 on average. This value indicate that the dominant Sr source of the Aral Sea is Mesozoic–Cenozoic carbonate rocks. The Rb–Sr systems of the silicate component of the bottom silt (which is likely dominated by eolian sediments) of MS and LT plot on the Т = 160 ± 5 Ma, I0 = 0.7091 ± 0.0001, pseudochron. The Rb–Sr systems of CB are less ordered, and the silt is likely a mixture of eolian and alluvial sediments.  相似文献   

13.
The East Tianshan is a remote Gobi area located in eastern Xinjiang, northwestern China. In the past several years, a number of gold, porphyry copper, and Fe(-Cu) and Cu-Ag-Pb-Zn skarn deposits have been discovered there and are attracting exploration interest.The East Tianshan is located between the Junggar block to the north and early Paleozoic terranes of the Middle Tianshan to the south. It is part of a Hercynian orogen with three distinct E-W-trending tectonic belts: the Devonian-Early Carboniferous Tousuquan-Dananhu island arc on the north and the Carboniferous Aqishan -Yamansu rift basin to the south, which are separated by rocks of the Kanggurtag shear zone. The porphyry deposits, dated at 322 Ma, are related to the late evolutionary stages of a subduction-related oceanic or continental margin arc. In contrast, the skarn, gold, and magmatic Ni-Cu deposits are associated with post-colli-sional tectonics at ca. 290-270 Ma. These Late Carboniferous - Early Permian deposits are associated with large-scale emplacement and eruption of magmas possibly caused by lithosphere delamination and rifting within the East Tianshan.  相似文献   

14.
The Huangsha Ag-rich tungsten deposit is genetically related to a buried granite which shows apparent vertical zoning in alteration.Greisen-type W(Mo) ores coccur at the top or the intrusive and sulfide-wolframite-quartz veins developed at the major stage of mineralization are present in low-grade metamorphic rocks in the outer-contacts.The veins exhibit a reversed zonation in the vertical section with silver concentrated in the lower part in association with sulfides.Micas,characterized by high Si and low Al.are extensively developed both in the granite and in the veins.They have similar cell parameters.belonging to 2M1 type,but those in the veins are understanding of the petrogenesis, evolution and mineralization of the granite.  相似文献   

15.
This paper examines how gender relations within rural communities in north-central Mexico affect women’s perceptions of and responses to environmental and social risks. Several studies currently exist which suggest various reasons as to how people especially vulnerable to the effects of climate change perceive their risks, and how this influences their responses. In this paper, I take a feminist approach to questions of social–environmental risks and adaptation to argue that risk perception is tightly linked to knowledge production, and knowledge production is a power-laden process involving the constant negotiation of resources, responsibilities and knowledge. I base this argument on the results of fieldwork conducted from September 2009 to May 2010 with women residents of two ejidos in northern Guanajuato, Mexico. In drawing from feminist political ecology studies, I intend to show how gender, environmental knowledge, risk perception and thus, adaptation are constituted by and embedded in social relations of power.  相似文献   

16.
F, Cl, S and P were determined, using electron microprobe, in magmatic inclusions trapped within minerals and glass mesostasis from Wudalianchi volcanic rocks. The initial volcanic magma from Wudalianchi corresponds to the basanitic magma crystallized near the surface ( pressure < 91 Mpa ). The potential H2O content of this magma is in the range 2 — 4 wt. %. The initial composition of volcanic magmas varies regularly from early to late volcanic events. From the Middle Pleistocene to the recent eruptions (1719 – 1721 yr.), the basicity of volcanic magma tends to increase, as reflected by an increase in MgO and CaO contents and by a progressive decrease in SiO2 and K2O contents. Meanwhile. from early (Q2 ) to late (Q3) episodic eruptions of the Middle Pleistocene, the initial concentrations of chlorine in volcanic magmas range from 1430 – 1930 ppm to 1700 ppm and decrease to 700 — 970 ppm for the first episodic eruption during the Holocene (Q 4 1 ). The chlorine concentrations of volcanic magmas of recent eruption (Q 4 2 ) are increased again to 2600 – 2870 ppm. A parallel evolution trend for phosphorus and chlorine concentrations in magmas has been certified: 1500 – 5970 ppm (Q2)→ 3500 – 4210 ppm (Q3)→ 1100– 3500 ppm (Q 4 1 )→ 6800– 7900 ppm (Q 4 2 ). The fluorine contents of volcanic magmas, from early to late volcanic events, show the same trend: 770 – 2470 ppm → 200–700 ppm → 700 – 800 ppm. During the crystallization-evolution of volcanic magmas, fluorine and phosphorus tend to be enriched in residual magmas as a result of crystal-melt differentiation. for example. the fluorine contents reach 5000– 6800 ppm and the phosphorus contents, 2.93wt.% in residual magmas. An appreciable amount of chlorine may be lost from water rich volcanic magmas prior to eruption as a result of degassing. Apparently, water serves as a gas carrier for the chlorine. The chlorine contents of residual magmas may decrease to 100 – 300 ppm. The volcanic magmas from Wudalianchi are poor in sulfur, normally ranging from 200 to 400ppm. On account of the behavior of sulfur in magmas and the strontium and oxygen isotopic analyses ((87Sr /86Sr)i=0.70503– 0.70589; δ18O = + 5.50 – + 6.89 ‰ ), it can be considered that the basanitic magmas in the Wudalianchi volcanic area came from the upper mantle and have not yet been contaminated probably by continental crust materials.  相似文献   

17.
《Geochimica et cosmochimica acta》1999,63(11-12):1853-1863
The oxidation states of Ni, Co, Mn, Cr, V and Si in magnesiowüstite have been determined in metal-oxide distribution experiments using a multi anvil apparatus at 9 and 18 GPa and 2200°C as a function of oxygen fugacity. Despite limitations to control oxygen fugacity by applying conventional buffering methods in high pressure experiments, a wide range of redox-conditions (3 log bar units) has been imposed to the metal-oxide partitioning experiments by varying the Si/O ratio of the starting material. The oxygen fugacity was calculated according to the Fe-FeO equilibrium between the run products. The ability to impose different oxygen fugacities by varying the starting material is confirmed by the large variation of element partitioning coefficients obtained at constant pressure and temperature. The calculated valences at both pressures investigated are divalent for Co, Mn, V and 4+ for Si. The results for Cr (∼2.5+) and Ni (∼1.5+) indicate non-ideal mixing of Ni and Cr in at least one of the product phases. Because the application of 1 bar activity coefficients for Ni and Cr in metal alloys does not change these valences, non-ideal mixing in magnesiowüstite or significantly larger non-ideal mixing properties of Ni and Cr in metal alloys at high pressure are likely to be responsible for the apparent valences. Omitting such non-ideal mixing properties when extrapolating high-pressure element partitioning data may be significant. The elements Cr, V and Mn become siderophile (DMmet/ox > 1) at 9–18 GPa and 2200°C at oxygen fugacities below IW-2.7 to IW-3.7. Considering, in addition, the influence of temperature, the depletion of Cr, Mn and V in the Earth’s mantle may be due, at least partly, to siderophile behavior at high pressure and temperature.  相似文献   

18.
INTRODUCTION Theinteractionofcomplextectonicphasesinthe IndusbasinduringtheCretaceoushasimpartedascal lopedoutlineinthesedimentarysequences.Thedevel opmentofdiversifiedsedimentaryformationsduringthe Cretaceousensuresexcellentsources(SembarandGoru formations)andreservoirs(MoghalKotandPabfor mations)forhydrocarbons.Numerousplaysandpros pectsofhydrocarbonareassociatedwiththeCretaceous system,consequentlytheIndusbasinisattractiveto petroleumexplorationcompaniesinPakistan(Sheikh andNa…  相似文献   

19.
Two sedimentary sections were measured at Tai Co (Co means lake in Tibetan) in western Tibet, China. The two sections are almost all composed of clay carbonate beds except in their lower parts where there are carbonized plants at >10 cm depths and dark-colored carbonate clay and clay at 50–70 cm depths, yielding abundant gastropods, ostracods, and charophytes. The carbon and oxygen stable isotope values of carbonate, ostracods, and charophytes and ecological features of microfossil communities indicate the following climatic change in the area from 41.4 to 4.5 ka BP: at 41.4–26.2 ka BP, the climate was relatively wet; at 26.2–25.5 ka BP, it was slightly warm-dry; at 25.5–22.5 ka BP, it was warm-wet; at 22.5–21.0 ka BP, it was slightly cold-wet; at 20.5–17.5 ka BP, it became cold abruptly and slightly wet, implying the climate of the last glacial maximum; at 17.5–16.0 ka BP, it was slightly cold-dry; at 16.0–11.8 ka BP, it was slightly warm-wet; at 11.8–10.4 ka BP, it was relatively cold-dry, roughly equivalent to the climate of the Younger Dryas, and at 10.4 ka BP, the temperatures began to rise again; at 10.4–9.4 ka BP, it was slightly warm-wet; at 9.4–8.5 ka BP, there occurred short warm-wet oscillations; at 8.5–7.9 ka BP, it was slightly dry-cold, representing a strong temperature-lowering and drying event in the postglacial stage; at 7.8–6.3 ka BP, it was slightly warm-wet; at 6.3–4.5 ka BP, the climate tended to be cold-dry. 4.5 ka BP recorded the maximum aridity since the late part of the late Pleistocene.  相似文献   

20.
The geodynamic setting of Mesozoic magmatic rocks and associated mineralization in eastern Tianshan, Northwest China, are attracting increasing attention. The newly discovered giant Donggebi molybdenum deposit (0.508 Mt at 0.115% Mo) is located in the central part of eastern Tianshan, Xinjiang. The molybdenum mineralization was genetically associated with the Donggebi stock, comprised of porphyritic granite and granite porphyry. Secondary ion mass spectrometry (SIMS) zircon U–Pb dating constrains that the porphyritic granite and granite porphyry emplacement occurred at 233.8 ± 2.5 Ma and 231.7 ± 2.6 Ma, respectively. The Re–Os model ages of six molybdenite samples range from 235.2 to 237.0 Ma, with a weighted mean age of 236.1 ± 1.4 Ma, which is roughly consistent within errors with the zircon U–Pb ages, suggesting a Middle Triassic magmatic–mineralization event at Donggebi. Geochemically, the Donggebi granitoids are characterized by high SiO2 and K2O contents, with low MgO contents, belonging to high-K calc-alkaline granites. These rocks show pronounced enrichment in K, Rb, U, and Pb, and depletion in Sr, Ba, P, and Ti, with negative Eu anomalies (Eu/Eu* = 0.20–0.38). In situ Hf isotopic analyses of zircon from the porphyritic granite and granite porphyry yielded εHf(t) values ranging from +6.6 to +10.5, and from +5.5 to +10.1, respectively. The geochemical and isotopic data imply that the primary magmas of the Donggebi granitoids could have originated by partial melting of a juvenile lower crust that involved some mantle components. Combined with the regional geological history, geochemistry of the Donggebi granitoids, and new isotopic age data, we thus propose that the Donggebi molybdenum deposit was formed in the Middle Triassic, and occurred in an intracontinental extension setting in eastern Tianshan.  相似文献   

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