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1.
Christophe L  cuyer 《Lithos》1990,25(4):243-259
The Trinity ophiolite consists of small magma chambers inside a large mantle body. Xenoliths of mantle peridotite occur both in gabbroic cumulates along the walls and in the matrices of ultrabasic breccias on the floors of the magma chambers. Field relationships and petrographic data suggest that these fragments of original mantle peridotite were modified by contact with basic magmas by modal metasomatism. Quantitative elemental mass transfers determined from the composition, volume and density variations of reacting minerals demonstrate both closed and open system conditions for the major (Si, Al, Ti, Na, Ca, Fe and Mg) and trace elements (Cr, Ni). In the open system, material gains and losses provide information on the composition of the fluid taking part in the metasomatic reaction.

During a first stage of metasomatism the mantle xenoliths were affected by high-temperature reactions at 600 to 925°C. They resulted from the interaction between solid mantle lherzolites and basic melts. The reactions are:

1. (1)those forming orthopyroxene-magnetite simplectite

2. (2)those forming plagioclase-magnetite corona

3. (3)clinopyroxene+spinel I→pargasitic hornblende+spinel II.

Chemical interactions between the upper mantle and oceanic magma chambers occurred as soon as the basic magmas had ascended through the upper mantle. The chemically modified magmas, within oceanic magma chambers, were depleted in Ti, Fe and Na. This could partly explain regional variations of the chemical compositions of primary magmas produced beneath slow-spreading ridges. The breakdown of olivine to orthopyroxene and magnetite participates in the control of the partition of magnetic Fe---Ti oxides between oceanic crust and mantle.

During the second stage, the serpentinization of olivine and the production of talc were superimposed on the products of the first stage. These reactions require large amounts of H2O. The hydrothermal fluid was probably seawater. It circulated in the brecciated area along the walls and floors of the magma chambers located at shallow depths. Such structural discontinuities thus played the role of penetration channels favoring seawater circulation in the oceanic crust.

All the chemical reactions examined suggest a significant open-system element transfer by infiltrating melts or circulating fluids. The results of this study suggest that caution is required in the interpretation of mineralogical and chemical information provided by mantle xenoliths carried to the surface by ascending magmas.  相似文献   

2.
Vegetation inherited from a Pliocene subtropical climate evolved through obliquity oscillations and global cooling leading to modern conditions. An integrated, highly time-resolved record of pollen and stable isotopes (δ18O and δ13C of Globigerina bulloides) was obtained to understand vegetation responses to Early Pleistocene climate changes. Continental and marine responses are compared in the Central Mediterranean region with a particular consideration of environmental changes during anoxic events.Pollen data illustrate vegetation dynamics as follows: [1] development of mesothermic elements (warm and humid conditions); [2] expansion of mid- and high-altitude elements (cooler but still humid conditions); and [3] strengthening of steppe and herb elements (cooler and dry conditions). These successions correlate with precession. δ18O variations recorded by Globigerina bulloides define two cycles (MIS 43-40) related to obliquity. At northern low- to mid-latitudes, the pollen signal records temperature and wetness changes related to precession even during global climate changes induced by obliquity. This may result in unexpected increasing wetness during glacial periods, which has to be considered specific to the Central and Eastern Mediterranean region. Lastly, an analysis of anoxic events reveals that enhanced runoff is indicated by increasing frequency of the riparian trees Liquidambar and Zelkova.  相似文献   
3.
International Journal of Earth Sciences - Four imbricated mafic to felsic plutons of Variscan age from Morocco have been investigated for their cooling history and geochemical interactions with...  相似文献   
4.
Apparent partition coefficients of Sr and Ba between calcium phosphate and water were measured experimentally for temperature ranging from 5°C to 60°C. Calcium phosphates were precipitated from an aqueous mixture of Na2HPO4 · 2H2O (10−2 M) and CaCl2 · 2H2O (10−2 M). Spiked solutions of Sr or Ba were introduced into the CaCl2 · 2H2O solution at Sr/Ca and Ba/Ca ratios of 0.1. The experiment consisted in sampling the liquid and solid phases after 1, 6, 48, and 96 h of interaction. The amorphous calcium phosphate (ACP) precipitated early in the experiment was progressively replaced by hydroxylapatite (HAP), except at 5°C where brushite (di-calcium phosphate di-hydrate or DCPD) was formed. We observed that the crystallinity of the solid phase increased with time for a given temperature and increased with temperature for a given time of reaction. With the exception of the experiment at 5°C, yield (R%) and apparent partition coefficients (Ka-wSr/Ca and Ka-wBa/Ca) both decreased with increasing reaction time. After 96 h, R%, Ka-wSr/Ca and Ka-wBa/Ca were observed to be constant, suggesting that the solid phases were at steady-state with respect to the aqueous solutions. The thermodependence of Sr and Ba partitioning between apatite and water at low temperature could therefore be calculated:
  相似文献   
5.
Intra-tooth δ18O variations within the carbonate (δ18Oc) and phosphate (δ18Op) components of tooth apatite were measured for Miocene and Pliocene hypsodont mammals from Afghanistan, Greece and Chad in order to evaluate the resistance of enamel to diagenetic alteration. Application of water-apatite interaction models suggest that the different kinetic behaviours of the phosphate-water and carbonate-water systems can be used to detect subtle oxygen isotope disequilibria in fossil enamel when intra-individual variations are considered. Selective alteration of the oxygen isotope composition from the carbonate component of Afghan and Greek enamels suggests inorganic isotopic exchange processes. Microbially-induced isotopic exchange for phosphate is demonstrated for the first time in enamel samples from Chad, in association with extensive recrystallization. In Chad, δ18Op values were derived from partial isotopic exchange with fossil groundwater during early diagenesis. Mass balance calculations using average carbonate content in enamel as a proxy for recrystallization, and the lowest δ18Op value of dentine as a proxy for the isotopic composition of the diagenetic fluid, indicate that diagenesis can alter δ18Op by as much as 3‰ in some enamel samples. This diagenetic alteration is also responsible for a decrease in intra-individual variations of up to 1‰ in affected specimens. The effects of diagenesis on δ18Op values of fossil enamel are not systematic, however, and can only be estimated if sequential δ18Op and δ18Oc analyses are performed on fossil enamel and dentine. Reconstruction of large temporal- or spatial-scale paleoclimates based on δ18Op analyses from mammalian teeth cannot be considered valid if enamel has been affected by bacterial activity or if the data cannot be corrected for diagenetic effects.  相似文献   
6.
Oxygen isotope compositions of biogenic phosphates from mammals are widely used as proxies of the isotopic compositions of meteoric waters that are roughly linearly related to the air temperature at high- and mid-latitudes. An oxygen isotope fractionation equation was determined by using present-day European arvicoline (rodents) tooth phosphate: δ18Op = 20.98(±0.59) + 0.572(±0.065) δ18Ow. This fractionation equation was applied to the Late Pleistocene karstic sequence of Gigny, French Jura. Comparison between the oxygen isotope compositions of arvicoline tooth phosphate and Greenland ice core records suggests to reconsider the previously established hypothetical chronology of the sequence. According to the δ18O value of meteoric water-mean air temperature relationships, the δ18O value of arvicoline teeth records variations in mean air temperatures that range from 0° to 15°C.  相似文献   
7.
Oxygen isotope compositions of phosphate in tooth enamel from large mammals (i.e. horse and red deer) were measured to quantify past mean annual air temperatures and seasonal variations between 145 ka and 33 ka in eastern France. The method is based on interdependent relationships between the δ18O of apatite phosphate, environmental waters and air temperatures. Horse (Equus caballus germanicus) and red deer (Cervus elaphus) remains have δ18O values that range from 14.2‰ to 17.2‰, indicating mean air temperatures between 7°C and 13°C. Oxygen isotope time series obtained from two of the six horse teeth show a sinusoidal-like signal that could have been forced by temperature variations of seasonal origin. Intra-tooth oxygen isotope variations reveal that at 145 ka, winters were colder (? 7 ± 2°C) than at present (3 ± 1°C) while summer temperatures were similar. Winter temperatures mark a well-developed West–East thermal gradient in France of about ? 9°C, much stronger than the ?4°C difference recorded presently. Negative winter temperatures were likely responsible for the extent and duration of the snow cover, thus limiting the food resources available for large ungulates with repercussions for Neanderthal predators.  相似文献   
8.
The middle Paleolithic stratigraphic sequence of Les Pradelles (Charente, France) spans from the end of Marine Isotope Stage (MIS) 4 until the middle of MIS 3. Micromammal remains are present in all the stratigraphic levels, offering a rare opportunity to address the questions of both environmental and climatic fluctuations throughout this period. Climate modes were studied through the taphonomy, biodiversity and oxygen isotope compositions of phosphate (δ18Op) from 66 samples of rodent tooth enamel. The δ18Op values from the lower sedimentary levels provide summer mean air temperatures of 19 ± 2°C (level 2/1) and of 16 ± 2°C (levels 2A, 2B and 4A). Within the middle of sequence (level 4B), a paleobiodiversity change can be identified with an increase of Dicrostonyx torquatus, which is associated with the largest amplitude in δ18Op values and the highest maximal δ18Op values. At the top of the sequence (level 5-2), a biodiversity change is observed with the increase of Microtus arvalis, but without any change in δ18Op values. The association of cold rodent species with unexpected high and large amplitudes in the δ18Op values of their teeth, possibly indicative of aridity, suggests their deposition during a Heinrich event.  相似文献   
9.
A semi-automatic, on-line method was developed to determine the δ13C and δ18O values of coexisting calcite and dolomite. An isotopic mass balance is used to calculate the compositions of dolomite after having measured that of calcite and of the “bulk” sample. The limit of validity of this method is established by performing isotopic measurements of artificial mixtures made of precisely weighted and isotopically-characterised dolomite and calcite. The accuracy and repeatability of the calculation of dolomite δ13C and δ18O are statistically determined with a Monte-Carlo procedure of error propagation. Stable isotope ratios are determined by using an automated MultiPrep™ system on-line with an isotope-ratio mass-spectrometer (IRMS). The reaction time and the temperature of reaction were optimised by comparing the results with the isotopic composition of known mixtures. The best results were obtained by phosphoric acid digestion after 20 min at 40 °C for calcite and 45 min at 90 °C for dolomite. This procedure allows an accurate determination of the isotopic ratios from small samples (300 μg). Application of this protocol to natural mixtures of calcite and dolomite requires the accurate determination of the relative abundance of calcite and dolomite by combining Mélières manocalcimetry (MMC) and X-ray diffractometry (XRD).  相似文献   
10.
Fluid inclusions represent a unique opportunity for a straightforward determination of the chemical and isotopic composition of fluids that composed the hydrosphere and atmosphere over Earth’s history. The production of reference materials in the laboratory is needed to monitor and to validate the determination of hydrogen and oxygen isotope compositions of water inclusions. We propose a protocol leading to the experimental synthesis of halite crystals that contain water inclusions whose δD and δ18O values can be related to those of surrounding evaporating waters where the crystals grew. Corrections to isotopic measurements were performed by applying an orthogonal projection of the raw data to the water evaporation trajectory line whose slope can be predicted by taking into account the parameters developed in the linear resistance model of Craig and Gordon (1965). Several hundreds of grams of halite reference material can be produced rapidly (within 2 d) at a low cost and can be stored within a vacuum desiccator at ambient temperature over several months or years. The described method is especially useful for the analysis of anhydrous salts and the interpretation of isotopic fractionations that operate within the surficial water cycle.  相似文献   
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