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Environmental geochemistry has attracted increasing interest during the last decade. In Sweden, geochemical mapping is carried out with methods that allow the data to be used in environmental research, including sampling plant roots and mosses from streams, soils and bedrock. These three sample types form an integrated strategy in environmental research, as well as in geochemical exploration. However, one problem that becomes prominent in geochemical mapping is to distinguish the signals derived from natural sources from those derived from anthropogenic sources. So far, this has mostly been done by using different types of samples, for example, different soil horizons. This is both expensive and time-consuming.We are currently developing alternative statistical solutions to this problem. The method used here is PLSR (partial least squares regression analysis). In this paper, we present an initial discussion on the applicability of PLSR in differentiating anthropogenic anomalies from natural contents.PLSR performs a simultaneous, interdependent principal component analysis decomposition in both X- and Y-matrices, in such a way that the information in the Y-matrix is used directly as a guide for optimal decomposition of the X-matrix. PLSR thus performs a generalized multivariate regression of Y on X overcoming the multicollinearity problem of correlated X-variables. The advantage of PLSR is that it gives optimal prediction ability in a strict statistical sense.Bedrock geochemistry from different lithologies in the mapping area in southern Sweden (Y-matrix) is analyzed together with stream or soil data (X-matrix). By modelling the PLS-regression between these two data sets, separate multivariate geochemical models based on the different bedrock types were developed. This step is called the training or modelling stage of the multivariate calibration. These calibrated models are subsequently used for predicting new (X) geochemical samples and estimating the corresponding Y-variable values. Information is obtained on how much of the metal contents in each new geochemical sample correlate with the different modelled bedrock types.By computing the appropriate X-residuals, we obtain information on the anthropogenic impact that is also carried by these new samples. In this way, it is possible from one single geochemical survey to derive both conventional geochemical background data and anthropogenic data, both of which can be readily displayed as maps.The present study concerns development of data analysis methods. Examples of the applications of the methodology are presented using Pb and U. The results show the share of these contents in different sampling media that is derived from bedrock on the one hand, and from anthropogenic sources, on the other. 相似文献
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The Al–Mg-rich granulites from the In Ouzzal craton, Algeria, show a great diversity of mineral reactions which correspond to continuous equilibria as predicted by phase relationships in the FeO–MgO–Al2O3–SiO2 system. The sequence of mineral reactions can be subdivided into three distinct stages: (1) a high-P stage characterized by the growth of coarse mineral assemblages involving sapphirine and the disappearance of early corundum and spinel-bearing assemblages; (2) a high-T stage characterized by the development of Sa–Qz-bearing assemblages; and (3) a later stage, in which garnet-bearing assemblages are replaced by more or less fine symplectites involving cordierite. During the course of early mineral reactions, the distribution coefficient, Kd, between the various ferromagnesian phases decreased significantly whereas Al2O3 in pyroxene increased concomitantly. These observations, when combined with topological constraints, clearly indicate that the high-P stage 1 was accompanied by a significant rise in temperature (estimated at 150 ± 50° C) under near isobaric conditions, in agreement with the reaction textures. By stage 2, pressure and temperature were extreme as evidenced by the low Kd value between orthopyroxene and garnet (Kd= 2.06–1.99), the high alumina content in pyroxene (up to 11.8%) and the high magnesium content in garnet [100 Mg/(Mg + Fe) = 60.6]. Mineral thermometry based on Fe–Mg exchange between garnet and pyroxene and on Al-solubility in pyroxene gives temperatures close to 970 ± 70° C at 10 ± 1.5 kbar. These results are in agreement with the development of Sa–Qz assemblages on a local scale. Late mineral reactions have been produced during a decompression stage from about 9 to 6 kbar. Except for local re-equilibration of Mg and Fe at grain boundaries, there is no evidence for further reactions below 700° C. We interpreted the whole set of mineral reactions as due to changes in pressure and temperature during a tectonic episode located at c. 2 Ga. Because of the lack of evidence for further uplift after the thermal relaxation which occurred at c. 6 kbar, it is possible however that the exhumation of this granulitic terrane occurred in a later tectonic event unrelated to its formation. 相似文献
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H. M. Tovmassian R. Kh. Hovhanessian R. A. Epremian D. Huguenin S. I. Serova V. G. Titov M. KH. Manarov 《Astrophysics and Space Science》1990,174(2):297-302
The results of UV-observations at 1640 Å of the regions of stellar associations Per OB1, Sco OB1, and Cyg OB1 made with the space telescope Glazar are presented. Respectively, 42, 22, and 30 hot stars brighter than 10m at 1640 Å were detected and measured in the mentioned stellar associations. A few of them are suspected to be variable in far UV. 相似文献
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Kim H. Esbensen Vagn F. Buchwald Dan J. Malvin John T. Wasson 《Geochimica et cosmochimica acta》1982,46(10):1913-1920
Concentrations of Re, Ir and Au are nearly constant within individual masses of the Cape York IIIAB iron meteorite, but differences between masses can be as large as a factor of 2, the extremes being Savik (5.1 μg/g Ir) and Agpalilik (2.7 μg/g Ir). The S concentration shows a still larger range from 13 mg/g in Agpalilik to 1.4 mg/g in Savik. A relatively large compositional hiatus between Dog and Agpalilik probably reflects inadequate sampling of the original material.Concentrations of Ir vary by ~10% and Au by ~3% between the ends of an 85-cm section from the Agpalilik mass of Cape York, but other sections through Agpalilik show smaller variations. These concentration ranges are much larger than expected from radial crystallization of a moderately large (radius 10 s of km) core. These variations in the Agpalilik mass may reflect dendritic crystallization, or they may have resulted from the process that produced the large concentration range among the Cape York masses.Large gradients in Re and Ir and small gradients in Ni and Au were also observed in samples within 2 cm of a large (100 cm3) troilite nodule. These gradients may reflect rapidly changing solid/liquid distribution coefficients during the final crystallization of S-rich liquid.The compositional trends among the various masses can either be explained by mixing of disparate end members followed by diffusive homogenization on a scale of m, or by dendritic crystallization on the ceiling of the IIIAB magma chamber. The mixing of a solid similar in composition to Savik with a liquid in equilibrium with this solid yields a good match to the observed trends, in which case Agpalilik consists of a mixture of 64% liquid and 36% solids. The bulk S content of the IIIAB core is calculated to be 14 mg/g on the basis of this model. 相似文献
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Geochemical exploration in secondary environments can be viewed as a particular manifestation of indirect geological observation. Geochemical anomalies in complex sample media reflect dispersion signatures, generally much disguised by secondary or higher-order mechanical and physico-chemical processes such as mixing, comminution, dilution, (re)transportation, weathering etc. Such complexities often make a thorough understanding of the origin of any particular sample type difficult ot obtain. The objective of data analysis in this context is to convert the geochemical data into a meaningful “signal”, particularly useful for prospecting, and other, in this case irrelevant, variability or “noise”. The experience of the last decades of practical exploration has clearly shown that statistical as well as geographical geochemical anomaly patterns are multi-element signatures. Using suitable multivariate statistical procedures (in the present case principal components modelling), it is possible to simultaneously define both a background data model and to quantify multivariate geochemical anomalies. This type of data analysis is guided very strongly by geological interaction, in which the emphasis is on modelling the background population(s), coupled with geographic plotting facilities. This outlier-screening facility is critical for many types of geochemical data evaluation. An example of this approach is described below. Another application of indirect multivariate data analysis is represented by PLS (Partial Least Squares) regression, which is a supervised pattern recognition and regression technique. We use it here to predict modal scheelite occurrences from regional stream-sediment data. 相似文献
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介绍了如何将互联网技术应用于石油行业的局域网或广域网中,在服务器端提供图形信息数据库的服务,并在客户端利用浏览器进行图形信息的查询,实现勘探开发图形信息的共享。 相似文献
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