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Isotope geochemistry of caliche developed on basalt   总被引：1，自引：0，他引：1  
Enormous variations in oxygen and carbon isotopes occur in caliche developed on < 3 Ma basalts in 3 volcanic fields in Arizona, significantly extending the range of δ18O and δ13C observed in terrestrial caliche. Within each volcanic field, δ18O is broadly co-variant with δ13C and increases as δ13C increases. The most 18O and 13C enriched samples are for subaerial calcite developed on pinnacles, knobs, and flow lobes that protrude above tephra and soil. The most 18O and 13C depleted samples are for pedogenic carbonate developed in soil atmospheres. The pedogenic caliche has δ18O fixed by normal precipitation in local meteoric waters at ambient temperatures and has low δ13C characteristic of microbial soil CO2. Subaerial caliche has formed from 18O-rich evapoconcentrated meteoric waters that dried out on surfaces after local rains. The associated 13C enrichment is due either to removal of 12C by photosynthesizers in the evaporating drops or to kinetic isotope effects associated with evaporation. Caliche on basalt lava flows thus initially forms with the isotopic signature of evaporation and is subsequently over-layered during burial by calcite carrying the isotopic signature of the soil environment. The large change in carbon isotope composition in subsequent soil calcite defines an isotopic biosignature that should have developed in martian examples if Mars had a “warm, wet” early period and photosynthesizing microbes were present in the early soils. The approach can be similarly applied to terrestrial Precambrian paleocaliche in the search for the earliest record of life on land. Large variations reported for δ18O of carbonate in Martian meteorite ALH84001 do not necessarily require high temperatures, playa lakes, or flood runoff if the carbonate is an example of altered martian caliche.  相似文献   
2.
The aim of this study is to apply an integrated approach to determine nitrate sources and fate in the alluvial aquifer of the River Vibrata (Abruzzi, central Italy) by coupling the Isotope and the Component approaches. Collected data include concentration and nitrogen isotope composition of groundwater samples from the alluvial aquifer and nitrogen loads arising from agricultural and non-agricultural sources. The adopted methodology identified synthetic fertilizers as main sources of nitrate in the Vibrata alluvial aquifer. At the catchment scale, two different zones have been identified: the Upper Valley, where infiltration to groundwater is dominant and nitrogen easily migrates into the aquifer; in this area, nitrate content in groundwater is stable and normally higher than EU requirements. Moreover, streamwaters are fed by groundwater with a nitrate content likely lowered by denitrification processes occurring in the hyporheic zone. In the Lower Valley, runoff processes dominate and the nitrate content in surface waters is higher. Nevertheless, groundwater is locally affected by denitrification that breaks down the nitrate content, which often reaches values consistent with law limits.  相似文献   
3.
Fluid–rock interaction was investigated in the inner aureole of the Late Miocene Monte Capanne pluton on Elba Island (Tuscany, central Italy) by integrating structural, petrological, fluid inclusion, and stable isotope analyses. In the north-western sector of the aureole (Procchio–Spartaia area), calc–silicates alternate with nearly pure carbonate layers at the metre scale. Close to the pluton, the prograde metamorphic sequence includes calc–silicates that transition within a few metres to overlying nearly pure calcite marbles. The calc–silicates are extensively metasomatised to form massive wollastonite-grossular-bearing exoskarn. The mineralogical assemblage found in the marbles and the unshifted carbon and oxygen isotopic ratios in calcite attest that the fluid phase was internally buffered. On the other hand, the calc–silicates constituted channels for infiltration of disequilibrium fluids of magmatic origin. Fluid infiltration was enhanced by hydrofracturing and structurally-controlled by existing planar anisotropies in calc–silicates (layering and lithological boundaries). At the metamorphic peak (∼600°C and 1.5–2 kbar), the marble–calc–silicate interface acted as a barrier to fluids exsolved from the crystallising intrusions, separating two different flow patterns in the inner aureole: a high fluid–flux region on its higher grade side (Wol-zone) and a low fluid–flux region on the lower-grade side (Cpx zone). Results of this study: (1) documented that fluid pathways in the aureole rocks at the top of the pluton were largely horizontal, controlled by the lithological layering and the pluton–host rock contact; and (2) elucidated the primary control exerted by the structural and rheological properties of the host rocks on the geometry of fluid flow during pluton emplacement.  相似文献   
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5.
The Ipanema alkaline-carbonatitic complex is part of the Meso-Cenozoic alkaline magmatism located within the southeastern part of the Brazilian Platform. Drill-core and field sampling have indicated the occurrence of glimmerites, with subordinate shonkinites (mela-syenites), clinopyroxene-bearing glimmerites, diorites and syenites. The glimmerites are cross-cut by lamprophyric dykes and calciocarbonatites. Fenitization has deeply affected the country rocks, originating dioritic and syenitic rocks. The Ipanema rocks show a distinct potassic affinity. The initial Sr-Nd- isotopic composition of the Ipanema rocks (87Sr/86Sr?=?0.70661–0.70754 and 143Nd/144Nd?=?0.51169–0.51181) is similar to that of tholeiitic and potassium-rich-alkaline rocks of the Eastern Paraguay. Stable isotope data for the Ipanema calciocarbonatite suggest interaction with fluids at temperatures typical of hydrothermal stages, as hypothesized for other carbonatite complexes from southeastern Brazil. The chemical differences between the lamprophyre, glimmerites, carbonatites, apatitites and magnetitites, and the absence of marked REE enrichment in the evolved lithologies, all indicate that fractional crystallization and accumulus of liquidus phases in a magma reservoir, likely coupled with liquid immiscibility processes, may have played an important role in the genesis of the Ipanema rocks.  相似文献   
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Magma-carbonate rock interaction is investigated through a geochemical and Sr-Nd-O isotope study of granular lithic clasts (ejecta) from the Alban Hills ultrapotassic volcano, Central Italy. Some samples (Group-1) basically represent intrusive equivalents of Alban Hills magmas. A few samples (Group-2) are ultramafic, have high MgO (∼30 to 40 wt%) and δ18O‰, and originated by accumulation of mafic phases that crystallised from ultrapotassic melts during assimilation of dolomitic rocks. Group-3 ejecta consist of dominant K-feldspar, and show major element compositions similar to phonolites, which, however, are absent among the Alban Hills volcanics. Finally, another group (Group-4) contains corroded K-feldspars, surrounded by a microgranular to porphyritic matrix, made of igneous minerals (K-feldspar, foids, clinopyroxene, phlogopite) plus wollastonite, garnet, and some cuspidine. Group-4 ejecta are depleted in SiO2 and enriched in CaO with respect to Group-3.The analysed ejecta have similar 143Nd/144Nd (0.51204-0.51217) as the Alban Hills lavas, whereas 87Sr/86Sr (0.70900-0.71067) is similar to lower. Whole rocks δ18O‰ ranges from +7.0 to +13.2, reaching maximum values in ultramafic samples. A positive correlation with CaO is observed in single rock groups. Large Ion Lithophile Element (LILE) abundances and REE fractionation are generally high, and extreme values of Th, U and LREE are found in some Group-3 and Group-4 rocks.Mineralogical, petrological and geochemical data reveal extensive interaction between magma and carbonate wall rocks, involving both dolostones and limestones. These processes had dramatic effects on magma compositions, especially on phonolites, which were transformed to foidites. Evidence of such a process is found in Group-4 samples, in which K-feldspar is observed to react with a matrix that represents strongly undersaturated melts formed by interaction between silicate magma and carbonates. Trace element data also testify to a very important role for F-CO2-H2O-S fluids during magma-wall rock interaction. Fluid transfer was responsible for extreme enrichments in Th, U, and LREE especially observed in Group-3 and Group-4 rocks. Implications of these processes for potassic magma evolution in Central Italy are discussed.  相似文献   
7.
International Journal of Earth Sciences - The Catalão II carbonatitic complex is part of the Alto Paranaíba Igneous Province (APIP), central Brazil, close to the Catalão I complex....  相似文献   
8.
Petrography-controlled laser ablation inductively coupled plasma mass spectrometry (LAICPMS) analyses of carbonate in fresh shallow level sub-volcanic Polino monticellite calcio-carbonatite tuffisite have been performed to assess the geochemical differences between fresh igneous, epigenetic carbonates and sedimentary accidental fragments. Igneous calcite has consistently high LREE/HREE ratios (La/Yb N , 15–130) due to high LREE (ΣLREE, 425–1,269 ppm). Secondary calcite cements are characterized by progressively lower and more variable trace element contents, with lower LREE/HREE ratios. A distinguishing geochemical feature is progressively increasing negative Ce anomalies observed through coarse secondary calcite that can be related to the surface environment processes. The limestone accidental fragments in the tuffisite have trace element contents almost two orders of magnitude lower than igneous carbonate and low LREE (ΣLREE < 9.5 ppm) with low LREE/HREE fractionation (La/Yb N ratios < 18). The stable isotope composition of different carbonate types is consistent with their formation in different environments. The tuffisitization processes during diatreme formation under high CO2-OH fugacity conditions may account for the differences noted in the igneous carbonates.  相似文献   
9.
Though the S. Susanna spring system is one of the biggest water sources in the central Apennines, its hydrogeological dynamics have been scarcely investigated. This study tried to clarify some of the factors controlling the recharge/discharge processes of this spring by modelling the available climate series, water balance equations and new isotopic and quantitative data, using statistical and raster overlay functions embedded in a Geographic Information System (GIS). Oxygen and hydrogen isotopic data were recorded monthly over a 2‐year period at the spring itself and in eight rain gauges in Reatini Mountains. The effective infiltration rate was calculated using the Kennessey coefficients and the Turc equation. Finally, the recharge area was identified with the help of an expert evaluation procedure. Local δ18O and δD versus altitude regression curves were used to validate the digital recharge model by comparing their expected values with the values actually measured. Recharge process was framed within the perspective of the ongoing local climate trends. The current discharge rate of 4·1 m3·s?1 is significantly lower than the average value of 5·5 m3·s?1 measured up to the 1980s, confirming the fall in the recharge/discharge rate. The hydrogeological system shows a delayed response, due to an average groundwater residence time in the aquifer, which is estimated to be about 15/20 years on the basis of the offset between calculated and observed isotope data at the main spring. For this reason the system is presently not equilibrated and is gradually changing towards a final equilibrium discharge estimated in about 3·4 m3·s?1. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   
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