山东碳酸岩磷灰石的特征及其研究意义

鲁中隆起的北缘分布着100多个燕山期的碳酸岩体。本文详细研究了岩体中磷灰石的一些重要特征,包括晶体形态、物理性质、光学常数、晶胞参数、化学成分、包裹体及钕锶同位素组成等。并据所得资料对岩体的成因,成岩物质来源等问题进行探讨。     

Hydrochemical and isotopic properties of the Mahmutlu and Bağdatoğlu mineralized thermal springs, Kırşehir, Turkey

The present study identifies the hydrochemical and isotopic properties of the Mahmutlu and Ba?dato?lu mineralized thermal springs in K?r?ehir province, a geothermal field in central Anatolia, Turkey. Based on these properties, a hydrogeological regime is proposed in order to explain the Mahmutlu–Ba?dato?lu geothermal system. The relation between the concentrations of the environmental stable isotopes deuterium and oxygen-18 in the water is similar to the relationship in global meteoric water, indicating that the water is of meteoric origin. Evaluation of the geochemical characteristics of the water reveals that these two thermal springs belong to the same hydrogeological system. The hydrogeological system comprises a fractured limestone member of the Çevirme Formation and the Kervansaray Formation as reservoir rocks, and the Delice?rmak Formation as an overlying aquitard. The waters of the Mahmutlu and Ba?dato?lu springs are mainly of the Na-Cl-SO4 type that originate from the Pohrenk evaporite. The thermal waters are undersaturated with respect to calcite, dolomite, halite, and gypsum. The δ 18O and δ 2H contents indicate a δ 18O shift in the Mahmutlu and Ba?dato?lu waters. The temperature range of the two reservoirs is estimated to be 98–158?°C, on the basis of Na+K+Ca and SiO2 geothermometers.     

Is there a stable isotope evidence for the CO2 fertilization effect?

It has been suggested that part of the so-called “missing sink” of carbon dioxide introduced into the atmosphere by anthropogenic activities, that is the imbalance between estimated anthropogenic carbon dioxide emissions and oceanic uptake, may be stored in the vegetation in midlatitudes. Precise mechanisms of abstraction of additional carbon dioxide by vegetation, also known as the “fertilization effect”, are poorly understood. Stable carbon and hydrogen isotope ratios of cellulose extracted from annual growth rings (covering the time period 1980–1993) in an oak tree from Kalamazoo, SW Michigan provide a basis to investigate at a physiological level how the fertilization effect may operate. The carbon isotope ratios show that the intercellular concentration of carbon dioxide increased due to an increase in stomatal opening. Although increased intercellular concentration of carbon dioxide translated to increased Water Use Efficiency and assimilation rates, it also resulted in increased transpiration rate as shown by higher D/H of the fixed carbon. The two-fold significance of the isotope data are: first, they provide the first field evidence based on isotope studies for excess CO₂ induced biomass production and second, they suggest that this mechanism is likely to operate only in limited environments. Vegetation in regions where moisture availability is not restricted so that there can be a gain in water use efficiency despite increased leaf evaporation are best suited to sequester excess carbon from the atmosphere.     

江西冷水坑矿床含矿花岗斑岩的Sr-Nd及锆石Hf-O同位素研究

江西冷水坑铅锌矿床是武夷成矿带北段的典型矿床,矿区内含矿花岗斑岩锆石U-Pb年龄为（162.0±2.0）Ma,岩浆分异程度较高,具有高SiO₂（69.46%~75.52%）、高K₂O（K₂O/Na₂O>3.22）、强过铝质（ASI=1.20~1.96）的特征。岩体发育较明显的Eu负异常,富集强不相容元素Rb、Th、U,而亏损高场强元素Ba、Sr、Nb、Ta、P、Ti。全岩同位素测试结果显示,冷水坑含矿花岗斑岩具有极高的⁸⁷Sr/⁸⁶Sr初始比值（0.74005~0.76518）与低的ε_Nd值（-11.48~-10.78）,锆石Hf-O同位素测定值变化范围较小,¹⁷⁶Hf/¹⁷⁷Hf介于0.282317~0.282460,具有负的ε_Hf（t）值（-12.39~-7.62）和相对较高的δ¹⁸O值（7.23‰~8.81‰）,指示岩浆主要来自于成熟地壳,可能起源于北武夷地区变质基底,源岩为基底变质岩,这可能与古太平洋板块俯冲形成的挤压背景下的地壳熔融有关。     

Fluid Geochemistry as Indicator of Tectonically-Related,Deep Water Circulations in the Sardinian Rift-Campidano Graben (Italy): New Insights from Environmental Isotopes

The EC funded Geochemical Seismic Zonation program (EEC GSZ Project 1996–1998) chose Sardinia as a low-seismicity site, in which the relationships between fluid geochemistry and seismo-tectonics had to be investigated and results compared with outcomes from other selected high-seismicity sites. A first article, examining the role of fault segmentation and seismic quiescence on the geochemical composition of groundwaters and gases, has already been presented (Angelone et al. 2005). This article deals with environmental isotopes which, together with selected hydrochemical data, give hints on tectonically-related fluid circulations. Four water-dominated hydrothermal systems were considered, all located along regional fault systems and discharging groundwaters belonging to the Na–HCO₃ and Na–Cl facies. In the considered systems, groundwater circulation takes place, principally, in the Palaeozoic Crystalline Basement (PCB), with the exception of the Logudoro system, where hydrological circuits develop in the Mesozoic Carbonate Platform (MCP). The high CO₂ contents, the non-attainment of fluid-rock equilibrium and the large lithological variability prevent the construction of a unique hydrogeological–geochemical conceptual model. In this case, stable isotopes provide a useful tool to describe the origin of fluids and their subterranean movements. Stable isotopes of water, integrated with hydrochemical data, indicate that fluids are derived from three main end members. The dominant component is a relatively recent local meteoric water; the second one is marine water; and the third one is a fossil freshwater, depleted in heavy isotopes with respect to modern rains. The latter end member entered the aquifer system in the past, when climatic conditions were greatly different from today. At least two circulation systems can be recognised, namely a shallow cold system and a deep hydrothermal system, as well as two distinct hydrological processes: (1) gravity-controlled descent of cold water towards greater depths and (2) convection linked to a thermal gradient, causing deep fluids to rise up from the hydrothermal reservoir towards the surface. The highly variable δ¹³C_TDIC values suggest the presence of two distinct CO₂ sources, namely, a biogenic one and a thermogenic one. The relation between the isotopic compositions of CO₂ and He indicates an increased mantle signature in uprising CO₂-rich fluids.     

The Upper Crustal Evolution of a Large Silicic Magma Body: Evidence from Crystal-scale Rb Sr Isotopic Heterogeneities in the Fish Canyon Magmatic System, Colorado

Batholith-sized bodies of crystal-rich magmatic ‘mush’are widely inferred to represent the hidden sources of manylarge-volume high-silica rhyolite eruptive units. Occasionallythese mush bodies are ejected along with their trapped interstitialliquid, forming the distinctive crystal-rich ignimbrites knownas ‘monotonous intermediates’. These ignimbritesare notable for their combination of high crystal contents (35–55%),dacitic bulk compositions with interstitial high-silica rhyoliticglass, and general lack of compositional zonation. The 5000km³ Fish Canyon Tuff is an archetypal eruption deposit of thistype, and is the largest known silicic eruption on Earth. Ejectafrom the Fish Canyon magmatic system are notable for the limitedcompositional variation that they define on the basis of whole-rockchemistry, whereas 45 vol. % crystals in a matrix of high-silicarhyolite glass together span a large range of mineral-scaleisotopic variability (microns to millimetres). Rb/Sr isotopicanalyses of single crystals (sanidine, plagioclase, biotite,hornblende, apatite, titanite) and sampling by micromillingof selected zones within glass plus sanidine and plagioclasecrystals document widespread isotopic disequilibrium at manyscales. High and variable ⁸⁷Sr/⁸⁶Sr_i values for euhedral biotitegrains cannot be explained by any model involving closed-systemradiogenic ingrowth, and they are difficult to rationalize unlessmuch of this radiogenic Sr has been introduced at a late stagevia assimilation of local Proterozoic crust. Hornblende is theonly phase that approaches isotopic equilibrium with the surroundingmelt, but the melt (glass) was isotopically heterogeneous atthe millimetre scale, and was therefore apparently contaminatedwith radiogenic Sr shortly prior to eruption. The other mineralphases (plagioclase, sanidine, titanite, and apatite) have significantlylower ⁸⁷Sr/⁸⁶Sr_i values than whole-rock values (as much as –0·0005).Such isotopic disequilibrium implies that feldspars, titaniteand apatite are antecrysts that crystallized from less radiogenicmelt compositions at earlier stages of magma evolution, whereashighly radiogenic biotite xenocrysts and the development ofisotopic heterogeneity in matrix melt glass appear to coincidewith the final stage of the evolution of the Fish Canyon magmabody in the upper crust. Integrated petrographic and geochemicalevidence is consistent with pre-eruptive thermal rejuvenationof a near-solidus mineral assemblage from 720 to 760°C (i.e.partial dissolution of feldspars + quartz while hornblende +titanite + biotite were crystallizing). Assimilation and blendingof phenocrysts, antecrysts and xenocrysts reflects chamber-wide,low Reynolds number convection that occurred within the last10 000 years before eruption. KEY WORDS: Fish Canyon Tuff; Rb–Sr isotopes; microsampling; magmatic processes; crystal mush     

Oxygen isotope composition and geothermometry of granulite to greenschist facies metamorphic rocks: a study from the Neoproterozoic collision-related nappe system, south of São Francisco Craton, SE Brazil

Oxygen isotope studies were carried out across units of a Neoproterozoic nappe system, south of São Francisco Craton. A temperature decrease toward the base of the system is found, consistent with a previously recognized inverted metamorphic pattern. The tectonic contact of the basal unit and the reworked southern São Francisco craton show a steep temperature gradient, suggesting that low temperature thrusting acted as the dominant tectonic process. The contrasts between the δ¹⁸O values of the Três Pontas-Varginha and Carmo da Cachoeira nappes and the differences among the samples and minerals are consistent with the preservation of sedimentary isotopic composition during metamorphism. The small differences in the δ¹⁸O values between the undeformed and the deformed calc-silicate samples (1.6‰) suggest that the δ¹⁸O value of mylonitization fluids was close to that which equilibrated with the metamorphic assemblage. The distinct δ¹⁸O values of metapelitic and calc-silicate samples and the great temperature difference from one type to the other indicate that no large-scale fluid interaction processes occurred during metamorphism. Oxygen isotopic estimations of both Três Pontas-Varginha undeformed rocks and Carmo da Cachoeira unaltered equivalents indicate δ¹⁸O values of up to 18‰. Comparison between these values and those from the ‘basement’ orthogneisses (8.3–8.5‰) indicates the latter are not sources for the metapelites.     

Deciphering the depositional environment of the laminated Crato fossil beds (Early Cretaceous,Araripe Basin,North‐eastern Brazil)

The laminated limestones of the Early Cretaceous Crato Formation of the Araripe Basin (North‐eastern Brazil) are world‐famous for their exceptionally well‐preserved and taxonomically diverse fossil fauna and flora. Whereas the fossil biota has received considerable attention, only a few studies have focused on the sedimentary characteristics and palaeoenvironmental conditions which prevailed during formation of the Crato Fossil Lagerstätte. The Nova Olinda Member represents the lowermost and thickest unit (up to 10 m) of the Crato Formation and is characterized by a pronounced rhythmically bedded, pale to dark lamination. To obtain information on palaeoenvironmental conditions, sample slabs derived from three local stratigraphic sections within the Araripe Basin were studied using high‐resolution multiproxy techniques including detailed logging, petrography, μ‐XRF scanning and stable isotope geochemistry. Integration of lithological and petrographic evidence indicates that the bulk of the Nova Olinda limestone formed via authigenic precipitation of calcite from within the upper water column, most probably induced and/or mediated by phytoplankton and picoplankton activity. A significant contribution from a benthonic, carbonate‐secreting microbial mat community is not supported by these results. Deposition took place under anoxic and, at least during certain episodes, hypersaline bottom water conditions, as evidenced by the virtually undisturbed lamination pattern, the absence of a benthonic fauna and by the occurrence of halite pseudomorphs. Input of allochthonous, catchment‐derived siliciclastics to the basin during times of laminite formation was strongly reduced. The δ¹⁸O values of authigenic carbonate precipitates (between ?7·1 and ?5·1‰) point to a ¹⁸O‐poor meteoric water source and support a continental freshwater setting for the Nova Olinda Member. The δ¹³C values, which are comparatively rich in ¹³C (between ?0·1 and +1·9‰), are interpreted to reflect reduced throughflow of water in a restricted basin, promoting equilibration with atmospheric CO₂, probably in concert with stagnant conditions and low input of soil‐derived carbon. Integration of lithological and isotopic evidence indicates a shift from closed to semi‐closed conditions towards a more open lake system during the onset of laminite deposition in the Crato Formation.     

Spatial geochemistry of a Carboniferous platform-margin-to-basin transect: Balancing environmental and diagenetic factors

Conventional (one-dimensional) chemostratigraphy of marine carbonates assesses the chemical archive of individual stratigraphic sections and their correlation in space and time. Whereas this approach has shown to be of value when linking isobathymetric domains, usually characterised by similar facies, more caution is needed when correlations are extended across different physiographic settings and hence different facies belts. Here, the spatial geochemical record of Pennsylvanian platform-margin-to-basin transects across a bathymetric range of about 800 m is documented and discussed in a process-oriented context. Particularly, the presence of layered palaeo-water masses and their potential control on slope facies distribution and geochemical properties requires attention. Whereas Carboniferous thermo- and/or chemo-clines most likely affected depth-related slope facies zonation, it was facies change and hence, variances in porosity–permeability properties, that controlled differential early burial diagenetic alteration. Specifically, the lower-slope related breccia facies is characterised by higher volumes of early burial carbonate cements. This implies that these sediments entered the shallow-burial domain with a considerable open pore space and gave way to an increased rock:fluid ratio. Whereas the δ¹³C record is invariant with bathymetry, the more diagenesis-sensitive δ¹⁸O proxy, records pronounced shifts observed across major facies boundaries. From this it is concluded that although the primary controlling factor of slope facies distribution with depth is probably palaeoceanographic in nature, it is differential rock:fluid ratios that control the first-order, spatial shifts in δ¹⁸O composition. These findings show that one-dimensional chemostratigraphy will severely underestimate the complexity of three-dimensional (bathymetric) data sets across platform margins. This is of relevance for the interpretation of the geochemical archive of fossil carbonate platforms in general.     

Geochronology,geochemistry, and mineralization of the granodiorite porphyry hosting the Matou Cu–Mo (±W) deposit,Lower Yangtze River metallogenic belt,eastern China

Porphyry and skarn Cu–Fe–Au–Mo deposits are widespread in the Middle and Lower Yangtze River metallogenic belt (MLYMB), eastern China. The Matou deposit has long been regarded as a typical Cu–Mo porphyry deposit within Lower Yangtze part of the belt. Recently, we identified scheelite and wolframite in quartz veins in the Matou deposit, which is uncommon in other porphyry and skarn deposits in the MLYMB. We carried out detailed zircon U–Pb dating and geochemical and Sr–Nd–Hf isotopic studies of the granodiorite porphyry at Matou to define any differences from other ore-related granitoids. The porphyry shows a SiO₂ content ranging from 61.85 wt.% to 65.74 wt.%, K₂O from 1.99 wt.% to 3.74 wt.%, and MgO from 1.74 wt.% to 2.19 wt.% (Mg^# value ranging from 45 to 55). It is enriched in light rare earth elements and large ion lithophile elements, but relatively depleted in Nb, Ta, Y, Yb and compatible trace elements (such as Cr, Ni, and V), with slight negative Eu anomalies (Eu/Eu^* = 0.88–0.98) and almost no negative Sr anomalies. Results of electron microprobe analysis of rock-forming silicate minerals indicate that the Matou porphyry has been altered by an oxidized fluid that is rich in Mg, Cl, and K. The samples show relatively low ε_Nd(t) values from −7.4 to −7.1, slightly high initial ⁸⁷Sr/⁸⁶Sr values from 0.708223 to 0.709088, and low ε_Hf(t) values of zircon from −9.0 to −6.5, when compared with the other Cu–Mo porphyry deposits in the MLYMB. Zircon U–Pb dating suggests the Matou granodiorite porphyry was emplaced at 139.5 ± 1.5 Ma (MSWD = 1.8, n = 15), which is within the age range of the other porphyries in the MLYMB. Although geochemical characteristics of the Matou and other porphyries in the MLYMB are similar and all adakitic, the detrital zircons in the samples from Matou suggest that Archean lower crust (2543 ± 29 Ma, MSWD = 0.25, n = 5) was involved with the generation of Matou magma, which is different from the other porphyries in the belt. Our study suggests that the Matou granodiorite porphyry originated from partial melting of thickened lower crust that was delaminated into the mantle, similar to the other porphyries in the MLYMB, but it has a higher proportion of lower crustal material, including Archean rocks, which contributed to the formation of the porphyry and related W-rich magmatic-hydrothermal system.