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341.
The nature of the petrogenetic links between carbonatites and associated silicate rocks is still under discussion (i.e., [Gittins J., Harmer R.E., 2003. Myth and reality of the carbonatite–silicate rock “association”. Period di Mineral. 72, 19–26.]). In the Paleozoic Kola alkaline province (NW Russia), the carbonatites are spatially and temporally associated to ultramafic cumulates (clinopyroxenite, wehrlite and dunite) and alkaline silicate rocks of the ijolite–melteigite series [(Kogarko, 1987), (Kogarko et al., 1995), (Verhulst et al., 2000), (Dunworth and Bell, 2001) and (Woolley, 2003)]. In the small (≈ 20 km2) Vuoriyarvi massif, apatite is typically a liquidus phase during the magmatic evolution and so it can be used to test genetic relationships. Trace elements contents have been obtained for both whole rocks and apatite (by LA-ICP-MS). The apatites define a single continuous chemical evolution marked by an increase in REE and Na (belovite-type of substitution, i.e., 2Ca2+ = Na+ + REE3+). This evolution possibly reflects a fractional crystallisation process of a single batch of isotopically homogeneous, mantle-derived magma.The distribution of REE between apatite and their host carbonatite have been estimated from the apatite composition of a carbonatite vein, belonging to the Neskevara conical-ring-like vein system. This carbonatite vein is tentatively interpreted as a melt. So, the calculated distribution coefficients are close to partition coefficients. Rare earth elements are compatible in apatite (D > 1) with a higher compatibility for the middle REE (DSm : 6.1) than for the light (DLa : 4.1) and the heavy (DYb : 1) REE.  相似文献   
342.
Pleistocene and Holocene peralkaline rhyolites from Torfajökull (South Iceland Volcanic Zone) and Ljósufjöll central volcanoes and trachytes from Snæfellsjökull (Snæfellsnes Volcanic Zone) allow the assessment of the mechanism for silicic magma genesis as a function of geographical location and crustal geothermal gradient. The low δ18O (2.4‰) and low Sr concentration (12.2 ppm) measured in Torfajökull rhyolites are best explained by partial melting of hydrated metabasaltic crust followed by major fractionation of feldspar. In contrast, very high 87Sr/86Sr (0.70473) and low Ba (8.7 ppm) and Sr (1.2 ppm) concentrations measured in Ljósufjöll silicic lavas are best explained by fractional crystallisation and subsequent 87Rb decay. Snæfellsjökull trachytes are also generated by fractional crystallisation, with less than 10% crustal assimilation, as inferred from their δ18O. The fact that silicic magmas within, or close to, the rift zone are principally generated by crustal melting whereas those from off-rift zones are better explained by fractional crystallisation clearly illustrates the controlling influence of the thermal state of the crust on silicic magma genesis in Iceland.  相似文献   
343.
The possibility of quantifying iron content in the topsoil of the slopes of the El Hacho Mountain complex in Southern Spain using imaging spectroscopy is investigated. Laboratory, field and airborne spectrometer (ROSIS) data are acquired, in combination with soil samples, which are analysed for dithionite extractable iron (Fed) content. Analysis of the properties of two iron related absorption features present in laboratory spectra demonstrates good relations, especially between the standard deviation (S.D.) of the values in an absorption feature and the Fed content (R2 = 0.67) as well as the ratio based Redness Index (R2 = 0.51). Such derived relations are less strong for the ROSIS data (R2 for S.D. = 0.26 and R2 for Redness Index = 0.22). The spatial distribution of iron in vegetated areas shows a strong sensitivity of these relations with the presence of vegetation. A combination of both methods shows that the overestimation of the Fed content with the one method is (partly) compensated by the underestimation with the other method.  相似文献   
344.
We experimentally studied the dacitic magma ejected during the first event in the Usu 2000 eruption to investigate the conditions of syneruptive magmatic ascent. Geophysical data revealed that the magma reached under West Nishiyama, the location of the event’s craters, after rising beneath the summit. Prior study of bubble-size distributions of ejecta shows two stages (stage 1 and stage 2) with different magma ascent rates, as the magma accelerated beneath West Nishiyama with the start of the second stage. To simulate ascent of stage 1 from the main reservoir, which was located at a depth of 4–6 km (125 MPa) to 2 km (50 MPa) beneath West Nishiyama, decompression experiments were conducted isothermally at 900°C following two paths. Single step decompression (SSD) samples were decompressed rapidly (0.67 MPa/s) to their final pressure and held for 12 to 144 hours. Multiple step decompression (MSD) samples were decompressed stepwise to their final pressure and quenched instantly. In MSD, the average decompression rates and total experimental durations varied between 0.01389 to 0.00015 MPa/s and 1.5 to 144 hours, respectively. Syneruptive crystallization was confined to stage 1, and the conditions of ascent were determined by documenting similarities in decompression-induced crystallization between ejecta and experiments. Core compositions, number densities, and shapes of experimental microlites indicate that ascent to 2 km depth occurred in less than 1.5 h. Volumes and number densities of experimental microlites from the SSD experiments that best replicate the decompression rate to 2 km indicate that the magma remained at 2 km for approximately 24 h before the eruption. Stagnation at a depth of 2 km corresponds with horizontal transport through a dike from beneath the summit to West Nishiyama, according to geodetic results. The total magma transport timescale including stage 2 is tens of hours and is shorter than the timescale of precursory seismicity (3.5 days), indicating that the erupted magma did not move out of the reservoir for the first 2 days. This is consistent with the temporal change in numbers of earthquakes, which reached a peak after 2 days.  相似文献   
345.
The chemical study shows that fahlores from the Prasolovka deposit are complex compounds with significant variations in their composition and the proportions of their constituent elements. Based on their major-element composition, they are subdivided into 3 species and 11 inter-and intra-species varieties. The chemical composition of the fahlores in different mineral assemblages from different ore types indicates that As fahlores subsequently replaced by Sb, Te-Sb, and Te fahlores during ore precipitation. The revealed evolution of the ore solutions from the early to late stages testifies that different ores at the Prasolovka deposit were formed under different physicochemical conditions.  相似文献   
346.
Aerosol samples were collected in the Atlantic marine boundary layer between the English Channel and Antarctica during November–December 1999. The composition of coarse (aerodynamic diameter 1–3 μm) individual aerosol particles was studied using the SEM/EDX method. The major particle types observed were fresh sea salt, sea-salt particles reacted partly or totally with sulphuric acid or nitric acid, Mg-sulphate, Ca-sulphate, mixed aluminosilicates and sea salt, aluminosilicates, Ca-rich particles and Fe-rich particles. The relative fractions of sea-salt particles with moderate or strong Cl depletion were high near the coasts of Europe (65–74%) and Northern Africa (44–87%), low far from the coast of Western Africa (10–20%) and very low in remote sea areas between Africa and Antarctica (1%). The Cl depletion was strongest when air masses arrived from the direction of anthropogenic pollution sources. The fractions of Mg-sulphate particles were high (18–25%) in 2 samples near Europe. The Mg-sulphate particles were probably formed as a result of fractional recrystallization of sea-salt particles in which Cl was substituted by sulphate. It remained unclear whether these particles were formed in the atmosphere or during and after sampling. The relative fractions of particles from continental sources were quite low (10–15%) near Europe, very high (25–78%) near the coast of Northwestern Africa and very low in the remote sea areas (0–2%). Most of the continental particles were aluminosilicates and some of them were internally mixed with sea salt. Near the coast of Northwestern Africa, the main source of aluminosilicates was Saharan dust, and near the Gulf of Guinea, emissions from biomass burning were also mixed with aluminosilicates and sea salt.  相似文献   
347.
As a result of their relative concentration towards the respectiveAtlantic margins, the silicic eruptives of the Paraná(Brazil)–Etendeka large igneous province are disproportionatelyabundant in the Etendeka of Namibia. The NW Etendeka silicicunits, dated at  相似文献   
348.
Two series of anhydrous experiments have been performed in anend-loaded piston cylinder apparatus on a primitive, mantle-derivedtholeiitic basalt at 1·0 GPa pressure and temperaturesin the range 1060–1330°C. The experimental data provideconstraints on phase equilibria, and solid and liquid compositionsalong the liquid line of descent of primary basaltic magmasdifferentiating in storage reservoirs located at the base ofthe continental crust. The first series are equilibrium crystallizationexperiments on a single basaltic bulk composition; the secondseries are fractionation experiments where near-perfect fractionalcrystallization was approached in a stepwise manner using 30°Ctemperature steps and starting compositions corresponding tothe liquid composition of the previous, higher-temperature glasscomposition. Liquids in the fractional crystallization experimentsevolve with progressive SiO2 increase from basalts to dacites,whereas the liquids in the equilibrium crystallization experimentsremain basaltic and display only a moderate SiO2 increase accompaniedby more pronounced Al2O3 enrichment. The principal phase equilibriacontrols responsible for these contrasting trends are suppressionof the peritectic olivine + liquid = opx reaction and earlierplagioclase saturation in the fractionation experiments comparedwith the equilibrium experiments. Both crystallization processeslead to the formation of large volumes of ultramafic cumulatesrelated to the suppression of plagioclase crystallization relativeto pyroxenes at high pressures. This is in contrast to low-pressurefractionation of tholeiitic liquids, where early plagioclasesaturation leads to the production of troctolites followed by(olivine-) gabbros at an early stage of differentiation. KEY WORDS: liquid line of descent; tholeiitic magmas; equilibrium crystallization; fractional crystallization  相似文献   
349.
铁矿物形成过程中的细菌作用研究   总被引:7,自引:2,他引:7       下载免费PDF全文
研究表明,细菌作用下形成针铁矿、水针铁矿和赤铁矿的过程中,细菌对矿物的作用贯穿于溶解吸附、络合、转换、结晶成核的全过程。细菌对矿物的作用具专属性。细菌作用不仅使原来矿物产生溶解、形成新矿物,生物化学显微环境的差异也可导致生成矿物的不同。同时细菌作用对矿物晶体结构、表面性质也产生影响。  相似文献   
350.
对南大别双河超高压岩板榴辉岩中锆石进行了阴极发光、喇曼光谱、U- Pb和氧同位素离子探针微区分析。发现大部分锆石具有核边结构 ,其核和边有明显不同的 U ,Th,Pb含量、Th/ U比、2 0 6 Pb/ 2 38U年龄和δ1 8O值。锆石边部具有变质锆石的结构和化学特征 ,核部具有岩浆锆石向变质锆石变化的过渡特征。 17个点 U - Pb同位素分析中大多数为不一致年龄 ,由 14个正向不一致点所构成的不一致线与一致曲线的上、下交点年龄分别为 2 4 89± 2 5和 2 4 8± 16 Ma,它们代表了榴辉岩原岩形成时间和前进变质至峰期变质过程中原岩岩浆锆石重结晶和变质增生作用的时间 ,大别山变质锆石的成因是复杂的 ,它既可以是变质新生锆石 ,呈独立的颗粒或原岩岩浆锆石的增生边 ,也可以是由原岩锆石在固相或流体存在下的重结晶作用形成。不同程度的重结晶作用是超高压条件下双河榴辉岩原岩岩浆锆石发生的主要的物理化学变化 ,它导致锆石中 U、Th、Pb和Th/ U比的降低和岩浆振荡环带的消退  相似文献   
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