The outlier sample effects on multivariate statistical data processing geochemical stream sediment survey (Moghangegh region, North West of Iran)

International Nuclear Information System (INIS)

Ghanbari, Y.; Habibnia, A.; Memar, A.

2009-01-01

In geochemical stream sediment surveys in Moghangegh Region in north west of Iran, sheet 1:50,000, 152 samples were collected and after the analyze and processing of data, it revealed that Yb, Sc, Ni, Li, Eu, Cd, Co, as contents in one sample is far higher than other samples. After detecting this sample as an outlier sample, the effect of this sample on multivariate statistical data processing for destructive effects of outlier sample in geochemical exploration was investigated. Pearson and Spear man correlation coefficient methods and cluster analysis were used for multivariate studies and the scatter plot of some elements together the regression profiles are given in case of 152 and 151 samples and the results are compared. After investigation of multivariate statistical data processing results, it was realized that results of existence of outlier samples may appear as the following relations between elements: - true relation between two elements, which have no outlier frequency in the outlier sample. - false relation between two elements which one of them has outlier frequency in the outlier sample. - complete false relation between two elements which both have outlier frequency in the outlier sample

Methodological approaches in estimating anomalous geochemical field structure

International Nuclear Information System (INIS)

Gavrilov, R; Rudmin, M

2015-01-01

Mathematical statistic methods were applied to analyze the core samples from vertical expendable wells in Chertovo Koryto gold ore field. The following methods were used to analyse gold in samples: assay tests and atomic absorption method (AAS), while emission spectrum semiquantative method was applied to identify traces. The analysis of geochemical association distribution in one central profile demonstrated that bulk metasomatic aureoles are characteristic of concentric zonal structure. The distribution of geochemical associations is correlated to the hydrothermal stages of mineral formation identified in this deposit. It was proved that the processed geochemical data by factor and cluster analyses provided additional information on the anomalous geochemical field structure in gold- bearing black-shale strata. Such methods are effective tools in interpretating specific features of geochemical field structures in analogous potential ore-bearing areas

Geochemical reanalysis of historical U.S. Geological Survey sediment samples from the Haines area, Juneau and Skagway quadrangles, southeast Alaska

Science.gov (United States)

Werdon, Melanie B.; Granitto, Matthew; Azain, Jaime S.

2015-01-01

The State of Alaska’s Strategic and Critical Minerals (SCM) Assessment project, a State-funded Capital Improvement Project (CIP), is designed to evaluate Alaska’s statewide potential for SCM resources. The SCM Assessment is being implemented by the Alaska Division of Geological & Geophysical Surveys (DGGS), and involves obtaining new airborne-geophysical, geological, and geochemical data. As part of the SCM Assessment, thousands of historical geochemical samples from DGGS, U.S. Geological Survey (USGS), and U.S. Bureau of Mines archives are being reanalyzed by DGGS using modern, quantitative, geochemical-analytical methods. The objective is to update the statewide geochemical database to more clearly identify areas in Alaska with SCM potential. The USGS is also undertaking SCM-related geologic studies in Alaska through the federally funded Alaska Critical Minerals cooperative project. DGGS and USGS share the goal of evaluating Alaska’s strategic and critical minerals potential and together created a Letter of Agreement (signed December 2012) and a supplementary Technical Assistance Agreement (#14CMTAA143458) to facilitate the two agencies’ cooperative work. Under these agreements, DGGS contracted the USGS in Denver to reanalyze historical USGS sediment samples from Alaska. For this report, DGGS funded reanalysis of 212 historical USGS sediment samples from the statewide Alaska Geochemical Database Version 2.0 (AGDB2; Granitto and others, 2013). Samples were chosen from the Chilkat, Klehini, Tsirku, and Takhin river drainages, as well as smaller drainages flowing into Chilkat and Chilkoot Inlets near Haines, Skagway Quadrangle, Southeast Alaska. Additionally some samples were also chosen from the Juneau gold belt, Juneau Quadrangle, Southeast Alaska (fig. 1). The USGS was responsible for sample retrieval from the National Geochemical Sample Archive (NGSA) in Denver, Colorado through the final quality assurance/quality control (QA/QC) of the geochemical

Instrumental neutron activation analysis of geochemical samples by k{sub 0} standardization method using short lived nuclides

Energy Technology Data Exchange (ETDEWEB)

Oura, Yasuji; Kanzaki, Chinatsu; Ebihara, Mitsuru [Tokyo Metropolitan Univ., Graduate School of Science, Tokyo (Japan)

2003-03-01

Mg, Al, Ca, Ti, V, and Mn contents in geochemical and cosmochemical samples were analyzed by both k{sub 0} standardization INAA and conventional INAA by a comparison method. The contents of Mg, Al, and Mn by k{sub 0} method were consistent with recommended values and ones by comparison methods. For Ti and V their values are slightly higher than recommended ones. The values by k{sub 0} method were reliable within {+-}10%. (author)

Geochemical mapping study of Panjang island

International Nuclear Information System (INIS)

Sutisna; Sumardjo

2010-01-01

Impact of industrial and regional development are not only related to an improvement of socio-economic, but also to an environmental conservation and sustainable. This impact could be observed on a change of geochemical mapping before and after an operational of the industry. In the relation with a regional development and resources utilization, the geochemical mapping have been done in the aim to know a resources and an elemental distribution at Panjang island. In this research, ko-Instrumental Neutron Activation Analysis (k_0-INAA) have been applied in an elemental quantification on the geochemical mapping. Pencuplikan of geochemical sample have been carried out by using a grid systematic method with a sample density of about 10 sample per square kilometre involved 85 pencuplikan point. The geochemical sample of sediment and soil have been provided as a dry weight of 100 mesh. Internal quality control have done by using a number of Standard Reference Materials obtained from US. Geological Survey. Fifteen elements of Sc, Co, In, Rb, Mo, Ba, Ce, Nd, Eu, La, Yb, Th, U, lr and Hf contained in standard materials have been evaluated. The analysis result show that a relative standard deviation less than 11 %, except for Mo (13 %) and lr (26 %). Fourteen elements of Al, Br, Ca, Co, Eu, Fe, La, U, Na, Ce, Mn, As, Sc and Th have been mapped and presented in this paper. The major elements of Ca, Al and Fe, and minor elements of Mn, U and Sc are distributed at all region. The lanthanide elements of La, Ce and Eu have vary concentration and could be found at the middle to the north of the island. (author)

Geochemical reanalysis of historical U.S. Geological Survey sediment samples from the Kougarok area, Bendeleben and Teller quadrangles, Seward Peninsula, Alaska

Science.gov (United States)

Werdon, Melanie B.; Granitto, Matthew; Azain, Jaime S.

2015-01-01

The State of Alaska’s Strategic and Critical Minerals (SCM) Assessment project, a State-funded Capital Improvement Project (CIP), is designed to evaluate Alaska’s statewide potential for SCM resources. The SCM Assessment is being implemented by the Alaska Division of Geological & Geophysical Surveys (DGGS), and involves obtaining new airborne-geophysical, geological, and geochemical data. As part of the SCM Assessment, thousands of historical geochemical samples from DGGS, U.S. Geological Survey (USGS), and U.S. Bureau of Mines archives are being reanalyzed by DGGS using modern, quantitative, geochemical-analytical methods. The objective is to update the statewide geochemical database to more clearly identify areas in Alaska with SCM potential. The USGS is also undertaking SCM-related geologic studies in Alaska through the federally funded Alaska Critical Minerals cooperative project. DGGS and USGS share the goal of evaluating Alaska’s strategic and critical minerals potential and together created a Letter of Agreement (signed December 2012) and a supplementary Technical Assistance Agreement (#14CMTAA143458) to facilitate the two agencies’ cooperative work. Under these agreements, DGGS contracted the USGS in Denver to reanalyze historical USGS sediment samples from Alaska. For this report, DGGS funded reanalysis of 302 historical USGS sediment samples from the statewide Alaska Geochemical Database Version 2.0 (AGDB2; Granitto and others, 2013). Samples were chosen from the Kougarok River drainage as well as smaller adjacent drainages in the Bendeleben and Teller quadrangles, Seward Peninsula, Alaska (fig. 1). The USGS was responsible for sample retrieval from the National Geochemical Sample Archive (NGSA) in Denver, Colorado through the final quality assurance/quality control (QA/QC) of the geochemical analyses obtained through the USGS contract lab. The new geochemical data are published in this report as a coauthored DGGS report, and will be incorporated

A comparison study on detection of key geochemical variables and factors through three different types of factor analysis

Science.gov (United States)

Hoseinzade, Zohre; Mokhtari, Ahmad Reza

2017-10-01

Large numbers of variables have been measured to explain different phenomena. Factor analysis has widely been used in order to reduce the dimension of datasets. Additionally, the technique has been employed to highlight underlying factors hidden in a complex system. As geochemical studies benefit from multivariate assays, application of this method is widespread in geochemistry. However, the conventional protocols in implementing factor analysis have some drawbacks in spite of their advantages. In the present study, a geochemical dataset including 804 soil samples collected from a mining area in central Iran in order to search for MVT type Pb-Zn deposits was considered to outline geochemical analysis through various fractal methods. Routine factor analysis, sequential factor analysis, and staged factor analysis were applied to the dataset after opening the data with (additive logratio) alr-transformation to extract mineralization factor in the dataset. A comparison between these methods indicated that sequential factor analysis has more clearly revealed MVT paragenesis elements in surface samples with nearly 50% variation in F1. In addition, staged factor analysis has given acceptable results while it is easy to practice. It could detect mineralization related elements while larger factor loadings are given to these elements resulting in better pronunciation of mineralization.

Application of Handheld Laser-Induced Breakdown Spectroscopy (LIBS) to Geochemical Analysis.

Science.gov (United States)

Connors, Brendan; Somers, Andrew; Day, David

2016-05-01

While laser-induced breakdown spectroscopy (LIBS) has been in use for decades, only within the last two years has technology progressed to the point of enabling true handheld, self-contained instruments. Several instruments are now commercially available with a range of capabilities and features. In this paper, the SciAps Z-500 handheld LIBS instrument functionality and sub-systems are reviewed. Several assayed geochemical sample sets, including igneous rocks and soils, are investigated. Calibration data are presented for multiple elements of interest along with examples of elemental mapping in heterogeneous samples. Sample preparation and the data collection method from multiple locations and data analysis are discussed. © The Author(s) 2016.

Application of the X-ray fluorescence analysis and X-ray diffraction in geochemical studies of the Pleistocene tills from Holy Cross Mountains

International Nuclear Information System (INIS)

Kubala-Kukuś, A.; Ludwikowska-Kedzia, M.; Banaś, D.; Braziewicz, J.; Majewska, U.; Pajek, M.; Wudarczyk-Moćko, J.

2013-01-01

X-ray fluorescence analysis methods (wavelength dispersive X-ray fluorescence analysis (WDXRF) and total reflection X-ray fluorescence (TXRF)) and X-ray powder diffraction (XRPD) have been applied in complementary geochemical studies of the Pleistocene till samples. The XRPD technique gave information about the mineral composition of the analyzed samples while the WDXRF and TXRF studies allowed the fast elemental analysis. The till samples were collected from different regions of Holy Cross Mountains (located in central Poland) which are still not unambiguously described in the context of the geochemical studies of the Quaternary sediments. The analysis was concentrated on the geochemical composition of the till samples both for materials occurring on the surface (characterized by continuous weathering processes) and for samples taken from core borehole. The overriding purpose of these studies is determination of the local lithotype of the tills and its lithologic and petrographic diagnostic properties, including the chemical composition of clay and minerals found in the clay. In the presented work the experimental sets up, sample preparation procedure and measurements programme will be discussed in details. Finally, the elemental and mineral compositions will be presented for studied different groups of the samples. - Highlights: • XRF analysis and X-ray diffraction used in studies of the till samples. • The till samples were collected from different regions of Holy Cross Mountains. • The analysis concentrates both on the samples from surface and from core borehole. • The purpose is determination of the local lithotype of the tills. • The experimental setup, sample preparation, measurements and results are discussed

Geochemical reanalysis of historical U.S. Geological Survey sediment samples from the northeastern Alaska Range, Healy, Mount Hayes, Nabesna, and Tanacross quadrangles, Alaska

Science.gov (United States)

Werdon, Melanie B.; Granitto, Matthew; Azain, Jaime S.

2015-01-01

The State of Alaska’s Strategic and Critical Minerals (SCM) Assessment project, a State-funded Capital Improvement Project (CIP), is designed to evaluate Alaska’s statewide potential for SCM resources. The SCM Assessment is being implemented by the Alaska Division of Geological & Geophysical Surveys (DGGS), and involves obtaining new airborne-geophysical, geological, and geochemical data. As part of the SCM Assessment, thousands of historical geochemical samples from DGGS, U.S. Geological Survey (USGS), and U.S. Bureau of Mines archives are being reanalyzed by DGGS using modern, quantitative, geochemical-analytical methods. The objective is to update the statewide geochemical database to more clearly identify areas in Alaska with SCM potential. The USGS is also undertaking SCM-related geologic studies in Alaska through the federally funded Alaska Critical Minerals cooperative project. DGGS and USGS share the goal of evaluating Alaska’s strategic and critical minerals potential and together created a Letter of Agreement (signed December 2012) and a supplementary Technical Assistance Agreement (#14CMTAA143458) to facilitate the two agencies’ cooperative work. Under these agreements, DGGS contracted the USGS in Denver to reanalyze historical USGS sediment samples from Alaska. For this report, DGGS funded reanalysis of 670 historical USGS sediment samples from the statewide Alaska Geochemical Database Version 2.0 (AGDB2; Granitto and others, 2013). Samples were chosen from the northeastern Alaska Range, in the Healy, Mount Hayes, Nabesna, and Tanacross quadrangles, Alaska (fig. 1). The USGS was responsible for sample retrieval from the National Geochemical Sample Archive (NGSA) in Denver, Colorado through the final quality assurance/quality control (QA/QC) of the geochemical analyses obtained through the USGS contract lab. The new geochemical data are published in this report as a coauthored DGGS report, and will be incorporated into the statewide geochemical

Multivariate analysis of ATR-FTIR spectra for assessment of oil shale organic geochemical properties

Science.gov (United States)

Washburn, Kathryn E.; Birdwell, Justin E.

2013-01-01

In this study, attenuated total reflectance (ATR) Fourier transform infrared spectroscopy (FTIR) was coupled with partial least squares regression (PLSR) analysis to relate spectral data to parameters from total organic carbon (TOC) analysis and programmed pyrolysis to assess the feasibility of developing predictive models to estimate important organic geochemical parameters. The advantage of ATR-FTIR over traditional analytical methods is that source rocks can be analyzed in the laboratory or field in seconds, facilitating more rapid and thorough screening than would be possible using other tools. ATR-FTIR spectra, TOC concentrations and Rock–Eval parameters were measured for a set of oil shales from deposits around the world and several pyrolyzed oil shale samples. PLSR models were developed to predict the measured geochemical parameters from infrared spectra. Application of the resulting models to a set of test spectra excluded from the training set generated accurate predictions of TOC and most Rock–Eval parameters. The critical region of the infrared spectrum for assessing S1, S2, Hydrogen Index and TOC consisted of aliphatic organic moieties (2800–3000 cm−1) and the models generated a better correlation with measured values of TOC and S2 than did integrated aliphatic peak areas. The results suggest that combining ATR-FTIR with PLSR is a reliable approach for estimating useful geochemical parameters of oil shales that is faster and requires less sample preparation than current screening methods.

Geochemical sensitivity analysis: Identification of important geochemical parameters for performance assessment studies

International Nuclear Information System (INIS)

Siegel, M.; Guzowski, R.; Rechard, R.; Erickson, K.

1986-01-01

The EPA Standard for geologic disposal of high level waste requires demonstration that the cumulative discharge of individual radioisotopes over a 10,000 year period at points 5 kilometers from the engineered barrier system will not exceed the limits prescribed in 40 CFR Part 191. The roles of the waste package, engineered facility, hydrogeology and geochemical processes in limiting radionuclide releases all must be considered in calculations designed to assess compliance of candidate repositories with the EPA Standard. In this talk, they will discuss the geochemical requirements of calculations used in these compliance assessments. In addition, they will describe the complementary roles of (1) simple models designed to bound the radionuclide discharge over the widest reasonable range of geochemical conditions and scenarios and (2) detailed geochemical models which can provide insights into the actual behavior of the radionuclides in the ground water. Finally, they will discuss development of sensitivity/uncertainty techniques designed to identify important site-specific geochemical parameters and processes using data from a basalt formation

Applications of prospecting geochemical techniques to the search for and to the study of uranium deposits in metropolitan France

International Nuclear Information System (INIS)

Grimbert, Arnold

1957-01-01

After having recalled facts which leaded the CEA to use new geochemical techniques for the prospecting of uranium deposits through sampling and analysis of soils and waters, the author describes the organisation and methods implemented for this prospecting activity: team composition for sampling and analysis, role of each engineer and technician in the prospecting stages (preliminary study, routine prospecting, result interpretation), sampling and analysis processes. He also reports campaigns of geochemical prospecting: study of the La Chapelle Largeau deposit (objectives, geological context, preliminary study, routine prospecting, study of geochemical anomalies), tactical research on Verneix indices (study of radioactivity anomaly discovered by radio-prospecting), strategical searches in a non prospected area in the South of Avallon. The author discusses the issues of efficiency and cost price of this geochemical prospecting technique in soils and in waters. Appendices present the equipment and operation modality for soil sampling, and for soil sample preparation, and principles, equipment and products for soil analysis and for water analysis [fr

Geochemical analysis of Minho Estuary sedimentary record and its contribution to palaeoenvironmental evolution

International Nuclear Information System (INIS)

Ivarez-Iglesias, P. A.

2009-01-01

Two sediment cores (∼30 m long) were retrieved at the mouth of the Minho Estuary to assess its palaeoenvironmental evolution for the last millennia. Samples were characterized by Energy-Dispersive X-Ray Fluorescence Spectrometry and Instrumental Neutron Activation Analysis, complemented by sedimentological analyses. Provenance of major and trace element contents (lithogenic or biogenic, continental or marine) is assessed. The influence of grain size effect on total element concentration is discussed. Most of the samples present a negative Eu anomaly. Sedimentological and geochemical parameters allow differentiating four geological units - fluvial, marine, estuarine and sand barrier - which reflects the temporal evolution of the Minho Estuary. (author)

Removal of iron interferences by solvent extraction for geochemical analysis by atomic-absorption spectrophotometry

Science.gov (United States)

Zhou, L.; Chao, T.T.; Sanzolone, R.F.

1985-01-01

Iron is a common interferent in the determination of many elements in geochemical samples. Two approaches for its removal have been taken. The first involves removal of iron by extraction with methyl isobutyl ketone (MIBK) from hydrochloric acid medium, leaving the analytes in the aqueous phase. The second consists of reduction of iron(III) to iron(II) by ascorbic acid to minimize its extraction into MIBK, so that the analytes may be isolated by extraction. Elements of interest can then be determined using the aqueous solution or the organic extract, as appropriate. Operating factors such as the concentration of hydrochloric acid, amounts of iron present, number of extractions, the presence or absence of a salting-out agent, and the optimum ratio of ascorbic acid to iron have been determined. These factors have general applications in geochemical analysis by atomic-absorption spectrophotometry. ?? 1985.

Semi-detailed uranium geochemical survey in Northwestern Samar (27 March 1979 - 4 July 1979)

International Nuclear Information System (INIS)

Santos, G. Jr.; Ogena, M.; Tauli, G.

1980-04-01

A uranium geochemical survey was conducted to delineate in detail the uranium prospective area(s) in northwestern Samar. A total of 805 stream sediments and 1.115 water samples were obtained from the target areas from uranium analysis. Geochemical anomalies were indicated in San Isidro and Mauo. Geochemical correlations between uranium and trace elements (Pb, Ag, Ni, Cu, Co, Zn and Mn) were generally poor. (ELC)

High resolution gamma-ray spectroscopy applied to bulk sample analysis

International Nuclear Information System (INIS)

Kosanke, K.L.; Koch, C.D.; Wilson, R.D.

1980-01-01

A high resolution Ge(Li) gamma-ray spectrometer has been installed and made operational for use in routine bulk sample analysis by the Bendix Field Engineering Corporation (BFEC) geochemical analysis department. The Ge(Li) spectrometer provides bulk sample analyses for potassium, uranium, and thorium that are superior to those obtained by the BFEC sodium iodide spectrometer. The near term analysis scheme permits a direct assay for uranium that corrects for bulk sample self-absorption effects and is independent of the uranium/radium disequilibrium condition of the sample. A more complete analysis scheme has been developed that fully utilizes the gamma-ray data provided by the Ge(Li) spectrometer and that more properly accounts for the sample self-absorption effect. This new analysis scheme should be implemented on the BFEC Ge(Li) spectrometer at the earliest date

Synthesizing Earth's geochemical data for hydrogeochemical analysis

Science.gov (United States)

Brantley, S. L.; Kubicki, J.; Miller, D.; Richter, D.; Giles, L.; Mitra, P.

2007-12-01

For over 200 years, geochemical, microbiological, and chemical data have been collected to describe the evolution of the surface earth. Many of these measurements are data showing variations in time or in space. To forward predict hydrologic response to changing tectonic, climatic, or anthropogenic forcings requires synthesis of these data and utilization in hydrogeochemical models. Increasingly, scientists are attempting to synthesize such data in order to make predictions for new regions or for future time periods. However, to make such complex geochemical data accessible requires development of sophisticated cyberinfrastructures that both invite uploading as well as usage of data. Two such cyberinfrastructure (CI) initiatives are currently developing, one to invite and promote the use of environmental kinetics data (laboratory time course data) through ChemxSeer, and the other to invite and promote the use of spatially indexed geochemical data for the Earth's Critical Zone through CZEN.org. The vision of these CI initiatives is to provide cyber-enhanced portals that encourage domain scientists to upload their data before publication (in private cyberspace), and to make these data eventually publicly accessible (after an embargo period). If the CI can be made to provide services to the domain specialist - e.g. to provide data analysis services or data comparison services - we envision that scientists will upload data. In addition, the CI can promote the use and comparison of datasets across disciplines. For example, the CI can facilitate the use of spatially indexed geochemical data by scientists more accustomed to dealing with time-course data for hydrologic flow, and can provide user-friendly interfaces with CI established to facilitate the use of hydrologic data. Examples of the usage of synthesized data to predict soil development over the last 13ky and its effects on active hydrological flow boundaries in surficial systems will be discussed for i) a N

Regional geochemical maps of the Tonopah 1 degree by 2 degrees Quadrangle, Nevada, based on samples of stream sediment and nonmagnetic heavy-mineral concentrate

Science.gov (United States)

Nash, J.T.; Siems, D.F.

1988-01-01

This report is part of a series of geologic, geochemical, and geophysical maps of the Tonopah 1° x 2° quadrangle, Nevada, prepared during studies of the area for the Conterminous United States Mineral Assessment Program (CUSMAP). Included here are 21 maps showing the distributions of selected elements or combinations of elements. These regional geochemical maps are based on chemical analyses of the minus-60 mesh (0.25 mm) fraction of stream-sediment samples and the nonmagnetic heavy-mineral concentrate derived from stream sediment. Stream sediments were collected at 1,217 sites. Our geochemical studies of mineralized rock samples provide a framework for evaluating the results from stream sediments.

Geochemical Interactions and Viral-Prokaryote Relationships in Freshwater Environments

Science.gov (United States)

Kyle, J. E.; Ferris, G.

2009-05-01

Viral and prokaryotic abundances were surveyed throughout southern Ontario aquatic habitats to determine relationships with geochemical parameters in the natural environment. Surface water samples were collected from acid mine drainage in summer of 2007 and 2008 and from circum-neutral pH environments in October to November 2008. Site determination was based on collecting samples from various aquatic habitats (acid mine drainage, lakes, rivers, tributaries, wetlands) with differing bedrock geology (limestone and shale dominated vs granitic Canadian Shield) to obtain a range of geochemical conditions. At each site, measurements of temperature, pH, and Eh were conducted. Samples collected for microbial counts and electron imaging were preserved to a final concentration of 2.5 % (v/v) glutaraldehyde. Additional sample were filtered into 60 mL nalgene bottles and amber EPA certified 40 mL glass vials to determine chemical constituents and dissolved organic carbon (DOC), respectively. Water was also collected to determine additional physiochemical parameters (dissolved total iron, ferric iron, nitrate, sulfate, phosphate, alkalinity, and turbidity). All samples were stored at 4 °C until analysis. Viral and prokaryotic abundance was determined by staining samples with SYBR Green I and examining with a epifluorescence microscope under blue excitation. Multiple regression analysis using stepwise backwards regression and general linear models revealed that viral abundance was the most influential predictor of prokaryotic abundance. Additional predictors include pH, sulfate, phosphate, and magnesium. The strength of the model was very strong with 90 % of the variability explained (R2 = 0.90, p < 0.007). This is the first report, to our knowledge, of viruses exhibiting such strong controls over prokaryotic abundance in the natural environment. All relationships are positively correlated with the exception of Mg, which is negatively correlated. Iron was also noted as a

Geochemical differentiation processes for arc magma of the Sengan volcanic cluster, Northeastern Japan, constrained from principal component analysis

Science.gov (United States)

Ueki, Kenta; Iwamori, Hikaru

2017-10-01

In this study, with a view of understanding the structure of high-dimensional geochemical data and discussing the chemical processes at work in the evolution of arc magmas, we employed principal component analysis (PCA) to evaluate the compositional variations of volcanic rocks from the Sengan volcanic cluster of the Northeastern Japan Arc. We analyzed the trace element compositions of various arc volcanic rocks, sampled from 17 different volcanoes in a volcanic cluster. The PCA results demonstrated that the first three principal components accounted for 86% of the geochemical variation in the magma of the Sengan region. Based on the relationships between the principal components and the major elements, the mass-balance relationships with respect to the contributions of minerals, the composition of plagioclase phenocrysts, geothermal gradient, and seismic velocity structure in the crust, the first, the second, and the third principal components appear to represent magma mixing, crystallizations of olivine/pyroxene, and crystallizations of plagioclase, respectively. These represented 59%, 20%, and 6%, respectively, of the variance in the entire compositional range, indicating that magma mixing accounted for the largest variance in the geochemical variation of the arc magma. Our result indicated that crustal processes dominate the geochemical variation of magma in the Sengan volcanic cluster.

Some results of NURE uranium geochemical studies

International Nuclear Information System (INIS)

Price, V. Jr.

1979-01-01

Some technical developments of the National Uranium Resource Evaluation Program which are of general application in geochemical exploration are being studied. Results of stream water and suspended and bottom sediment analyses are compared for an area near Williamsport, Pennsylvania. Variations of uranium content of water samples with time in the North Carolina Piedmont are seen to correlate with rainfall. Ground water samples from coastal and piedmont areas were analyzed for helium. All media sampled provide useful information when properly analyzed and interpreted as part of a total geological analysis of an area

A comparison of iron oxide-rich joint coatings and rock chips as geochemical sampling media in exploration for disseminated gold deposits

Science.gov (United States)

Crone, W.; Larson, L.T.; Carpenter, R.H.; Chao, T.T.; Sanzolone, R.F.

1984-01-01

We evaluated the effectiveness of iron oxide-rich fracture coatings as a geochemical sampling medium for disseminated gold deposits, as compared with conventional lithogeochemical methods, for samples from the Pinson mine and Preble prospect in southeastern Humboldt County, Nevada. That disseminated gold mineralization is associated with Hg, As, and Sb is clearly demonstrated in these deposits for both fracture coatings and rock chip samples. However, the relationship is more pronounced for fracture coatings. Fracture coatings at Pinson contain an average of 3.61, 5.13, 14.37, and 3.42 times more Au, As, Sb and Hg, respectively, than adjacent rock samples. At Preble, fracture coatings contain 3.13, 9.72, 9.18, and 1.85 times more Au, As, Sb and Hg, respectively, than do adjacent rock samples. Geochemical anomalies determined from fracture coatings are thus typically more intense than those determined from rock samples for these elements. The sizes of anomalies indicated by fracture coatings are also somewhat larger, but this is less obvious. In both areas, Sb anomalies are more extensive in fracture coatings. At Preble, some Hg and Au anomalies are also more extensive in fracture coatings. In addition to halos formed by the Hg, As and Sb, high values for Au/Ag and Zn/(Fe + Mn) are closely associated with gold mineralization at the Pinson mine. The large enhancement in geochemical response afforded by fracture coatings indicates a definite potential in the search for buried disseminated gold deposits. ?? 1984.

A geochemical atlas of North Carolina, USA

Science.gov (United States)

Reid, J.C.

1993-01-01

very general indication of geochemical distribution patterns and should not be used for site specific studies. The atlas maps for each element were computer-generated at the state's geographic information system (Center for Geographic Information and Analysis [CGIA]). The Division of Statistics and Information Services provided input files. The maps in the atlas are point maps. Each sample is represented by a symbol generally corresponding to a quartile class. Other reports will transmit sample and analytical data for state regions. Data are tentatively planned to be available on disks in spreadsheet format for personal computers. During the second phase of this project, stream-sediment samples are being assigned to state geologic map unit names using a GIS system to determine background and anomaly values. Subsequent publications will make this geochemical data and accompanying interpretations available to a wide spectrum of interdisciplinary users. ?? 1993.

Application of integrated Landsat, geochemical and geophysical data in mineral exploration

International Nuclear Information System (INIS)

Conradsen, K.; Nilsson, G.; Thyrsted, T.; Gronlands Geologiske Undersogelse, Copenhagen, Denmark)

1985-01-01

In South Greenland (20000 sq. km) a remote sensing investigation is executed in connection with uranium exploration. The investigation includes analysis of Landsat data, conversion of geological, geochemical and geophysical data to image format compatible with Landsat images, and analysis of the total set of integrated data. The available geochemical data consisted of samples from 2000 sites, analyzed for U, K, Rb, Sr, Nb, Ga, Y, and Fe. The geophysical data comprised airborne gamma-spectrometric measurements and aeromagnetic data. The interpolation routines consisted of a kriging procedure for the geochemical data and a minimum curvature routine for the geophysical data. The analysis of the integrated data set is at a preliminary stage. As example a composite image showing Landsat channel 7, magnetic values, and Fe values as respectively intensity, hue and saturation is analyzed. It reveals alkaline intrusions and basaltic layers as anomalies while other anomalies cannot be accounted for on the basis of the present geological knowledge. 12 references

Quest to identify geochemical risk factors associated with chronic kidney disease of unknown etiology (CKDu) in an endemic region of Sri Lanka-a multimedia laboratory analysis of biological, food, and environmental samples.

Science.gov (United States)

Levine, Keith E; Redmon, Jennifer Hoponick; Elledge, Myles F; Wanigasuriya, Kamani P; Smith, Kristin; Munoz, Breda; Waduge, Vajira A; Periris-John, Roshini J; Sathiakumar, Nalini; Harrington, James M; Womack, Donna S; Wickremasinghe, Rajitha

2016-10-01

The emergence of a new form of chronic kidney disease of unknown etiology (CKDu) in Sri Lanka's North Central Province (NCP) has become a catastrophic health crisis. CKDu is characterized as slowly progressing, irreversible, and asymptomatic until late stages and, importantly, not attributed to diabetes, hypertension, or other known risk factors. It is postulated that the etiology of CKDu is multifactorial, involving genetic predisposition, nutritional and dehydration status, exposure to one or more environmental nephrotoxins, and lifestyle factors. The objective of this limited geochemical laboratory analysis was to determine the concentration of a suite of heavy metals and trace element nutrients in biological samples (human whole blood and hair) and environmental samples (drinking water, rice, soil, and freshwater fish) collected from two towns within the endemic NCP region in 2012 and 2013. This broad panel, metallomics/mineralomics approach was used to shed light on potential geochemical risk factors associated with CKDu. Based on prior literature documentation of potential nephrotoxins that may play a role in the genesis and progression of CKDu, heavy metals and fluoride were selected for analysis. The geochemical concentrations in biological and environmental media areas were quantified. Basic statistical measurements were subsequently used to compare media against applicable benchmark values, such as US soil screening levels. Cadmium, lead, and mercury were detected at concentrations exceeding US reference values in many of the biological samples, suggesting that study participants are subjected to chronic, low-level exposure to these elements. Within the limited number of environmental media samples, arsenic was determined to exceed initial risk screening and background concentration values in soil, while data collected from drinking water samples reflected the unique hydrogeochemistry of the region, including the prevalence of hard or very hard water, and

The geochemical atlas of Alaska, 2016

Science.gov (United States)

Lee, Gregory K.; Yager, Douglas B.; Mauk, Jeffrey L.; Granitto, Matthew; Denning, Paul; Wang, Bronwen; Werdon, Melanie B.

2016-06-21

A rich legacy of geochemical data produced since the early 1960s covers the great expanse of Alaska; careful treatment of such data may provide significant and revealing geochemical maps that may be used for landscape geochemistry, mineral resource exploration, and geoenvironmental investigations over large areas. To maximize the spatial density and extent of data coverage for statewide mapping of element distributions, we compiled and integrated analyses of more than 175,000 sediment and soil samples from three major, separate sources: the U.S. Geological Survey, the National Uranium Resource Evaluation program, and the Alaska Division of Geological & Geophysical Surveys geochemical databases. Various types of heterogeneity and deficiencies in these data presented major challenges to our development of coherently integrated datasets for modeling and mapping of element distributions. Researchers from many different organizations and disparate scientific studies collected samples that were analyzed using highly variable methods throughout a time period of more than 50 years, during which many changes in analytical techniques were developed and applied. Despite these challenges, the U.S. Geological Survey has produced a new systematically integrated compilation of sediment and soil geochemical data with an average sample site density of approximately 1 locality per 10 square kilometers (km2) for the entire State of Alaska, although density varies considerably among different areas. From that compilation, we have modeled and mapped the distributions of 68 elements, thus creating an updated geochemical atlas for the State.

Pilot studies for the North American Soil Geochemical Landscapes Project - Site selection, sampling protocols, analytical methods, and quality control protocols

Science.gov (United States)

Smith, D.B.; Woodruff, L.G.; O'Leary, R. M.; Cannon, W.F.; Garrett, R.G.; Kilburn, J.E.; Goldhaber, M.B.

2009-01-01

In 2004, the US Geological Survey (USGS) and the Geological Survey of Canada sampled and chemically analyzed soils along two transects across Canada and the USA in preparation for a planned soil geochemical survey of North America. This effort was a pilot study to test and refine sampling protocols, analytical methods, quality control protocols, and field logistics for the continental survey. A total of 220 sample sites were selected at approximately 40-km intervals along the two transects. The ideal sampling protocol at each site called for a sample from a depth of 0-5 cm and a composite of each of the O, A, and C horizons. The Ca, Fe, K, Mg, Na, S, Ti, Ag, As, Ba, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Ga, In, La, Li, Mn, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Te, Th, Tl, U, V, W, Y, and Zn by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry following a near-total digestion in a mixture of HCl, HNO3, HClO4, and HF. Separate methods were used for Hg, Se, total C, and carbonate-C on this same size fraction. Only Ag, In, and Te had a large percentage of concentrations below the detection limit. Quality control (QC) of the analyses was monitored at three levels: the laboratory performing the analysis, the USGS QC officer, and the principal investigator for the study. This level of review resulted in an average of one QC sample for every 20 field samples, which proved to be minimally adequate for such a large-scale survey. Additional QC samples should be added to monitor within-batch quality to the extent that no more than 10 samples are analyzed between a QC sample. Only Cr (77%), Y (82%), and Sb (80%) fell outside the acceptable limits of accuracy (% recovery between 85 and 115%) because of likely residence in mineral phases resistant to the acid digestion. A separate sample of 0-5-cm material was collected at each site for determination of organic compounds. A subset of 73 of these samples was analyzed for a suite of

A procedure for partitioning bulk sediments into distinct grain-size fractions for geochemical analysis

Science.gov (United States)

Barbanti, A.; Bothner, Michael H.

1993-01-01

A method to separate sediments into discrete size fractions for geochemical analysis has been tested. The procedures were chosen to minimize the destruction or formation of aggregates and involved gentle sieving and settling of wet samples. Freeze-drying and sonication pretreatments, known to influence aggregates, were used for comparison. Freeze-drying was found to increase the silt/clay ratio by an average of 180 percent compared to analysis of a wet sample that had been wet sieved only. Sonication of a wet sample decreased the silt/clay ratio by 51 percent. The concentrations of metals and organic carbon in the separated fractions changed depending on the pretreatment procedures in a manner consistent with the hypothesis that aggregates consist of fine-grained organic- and metal-rich particles. The coarse silt fraction of a freeze-dried sample contained 20–44 percent higher concentrations of Zn, Cu, and organic carbon than the coarse silt fraction of the wet sample. Sonication resulted in concentrations of these analytes that were 18–33 percent lower in the coarse silt fraction than found in the wet sample. Sonication increased the concentration of lead in the clay fraction by an average of 40 percent compared to an unsonicated sample. Understanding the magnitude of change caused by different analysis protocols is an aid in designing future studies that seek to interpret the spatial distribution of contaminated sediments and their transport mechanisms.

Air-segmented continuous-flow analysis for molybdenum in various geochemical samples

International Nuclear Information System (INIS)

Harita, Y.; Sugiyama, M.; Hori, T.

2003-01-01

An air-segmented continuous-flow method has been developed for the determination of molybdenum at ultra trace levels using the catalytic effect of molybdate during the oxidation of L-ascorbic acid by hydrogen peroxide. Incorporation of an on-line ion exchange column improved the tolerance limit for various ions. The detection limits with and without the column were 64 pmol L m1 and 17 pmol L m1 , and the reproducibilities at 10 nmol L m1 were 2.1 % and 0.2 %, respectively. The proposed method was applied to the determination of molybdenum in seawater and lake water as well as in rock and sediment samples. This method has the highest sensitivity among the available literature to our knowledge, and is also convenient for routine analysis of molybdenum in various natural samples. (author)

Geochemical baseline studies of soil in Finland

Science.gov (United States)

Pihlaja, Jouni

2017-04-01

The soil element concentrations regionally vary a lot in Finland. Mostly this is caused by the different bedrock types, which are reflected in the soil qualities. Geological Survey of Finland (GTK) is carrying out geochemical baseline studies in Finland. In the previous phase, the research is focusing on urban areas and mine environments. The information can, for example, be used to determine the need for soil remediation, to assess environmental impacts or to measure the natural state of soil in industrial areas or mine districts. The field work is done by taking soil samples, typically at depth between 0-10 cm. Sampling sites are chosen to represent the most vulnerable areas when thinking of human impacts by possible toxic soil element contents: playgrounds, day-care centers, schools, parks and residential areas. In the mine districts the samples are taken from the areas locating outside the airborne dust effected areas. Element contents of the soil samples are then analyzed with ICP-AES and ICP-MS, Hg with CV-AAS. The results of the geochemical baseline studies are published in the Finnish national geochemical baseline database (TAPIR). The geochemical baseline map service is free for all users via internet browser. Through this map service it is possible to calculate regional soil baseline values using geochemical data stored in the map service database. Baseline data for 17 elements in total is provided in the map service and it can be viewed on the GTK's web pages (http://gtkdata.gtk.fi/Tapir/indexEN.html).

The U-tube sampling methodology and real-time analysis of geofluids

International Nuclear Information System (INIS)

Freifeld, Barry; Perkins, Ernie; Underschultz, James; Boreham, Chris

2009-01-01

The U-tube geochemical sampling methodology, an extension of the porous cup technique proposed by Wood (1973), provides minimally contaminated aliquots of multiphase fluids from deep reservoirs and allows for accurate determination of dissolved gas composition. The initial deployment of the U-tube during the Frio Brine Pilot CO 2 storage experiment, Liberty County, Texas, obtained representative samples of brine and supercritical CO 2 from a depth of 1.5 km. A quadrupole mass spectrometer provided real-time analysis of dissolved gas composition. Since the initial demonstration, the U-tube has been deployed for (1) sampling of fluids down gradient of the proposed Yucca Mountain High-Level Waste Repository, Armagosa Valley, Nevada (2) acquiring fluid samples beneath permafrost in Nunuvut Territory, Canada, and (3) at a CO 2 storage demonstration project within a depleted gas reservoir, Otway Basin, Victoria, Australia. The addition of in-line high-pressure pH and EC sensors allows for continuous monitoring of fluid during sample collection. Difficulties have arisen during U-tube sampling, such as blockage of sample lines from naturally occurring waxes or from freezing conditions; however, workarounds such as solvent flushing or heating have been used to address these problems. The U-tube methodology has proven to be robust, and with careful consideration of the constraints and limitations, can provide high quality geochemical samples.

Assessment Cu, Ni and Zn Pollution in the Surface Sediments in the Southern Peninsular Malaysia using Cluster Analysis, Ratios of Geochemical Nonresistant to Resistant Fractions, and Geochemical Indices

Directory of Open Access Journals (Sweden)

Yap. C. K.

2011-01-01

Full Text Available The intertidal sediment samples collected in May 2007 from 12 sampling sites in the southern part of Peninsular Malaysia, were determined for the total concentrations of Cu, Ni and Zn and their four geochemical fractions. The total concentrations (μg/g dry weight of Cu, Ni and Zn ranged from 9.48 to 115.82, 12.95 to 36.18 and 45.35 to 136.56, respectively. The ratios of nonresistant to resistant fractions based on geochemical analysis revealed that the Pantai Lido and Senibong had > 1.0, indicating > 50% of the total concentrations of Cu, Ni and Cu were contributed by anthropogenic sources. This is well complemented by the cluster analysis in which Pantai Lido and Senibong are clustered together based on the three metals clustering pattern. By using Fe as a normalizing element, Cu found at Pantai Lido and Senibong showed > 1.5 for the enrichment factor (EF, which indicated that the Cu was delivered from non-crustal materials or anthropogenic origins while all sampling sites showed Ni and Zn may be entirely from crustal materials. Based on the geoaccumulation index (Igeo (Müller, 1981, similar pattern was also found for Pantai Lido and Senibong in which again only Cu concentrations ranged from 1-2, indicating 'moderate pollution' (Igeo 1 < 2; Class 2.while other sites can be considered as 'unpolluted' (Igeo < 0; Class 0 by Cu, Ni and Zn. Ratios of NR/R exhibited better in the assessment of polluted sites while EF and Igeo should be revised according to Malaysian sedimentary characteristics. This study should prompt more biochemical and molecular studies on the intertidal molluscs from the Straits of Johore since the identified two sites are located in the Straits of Johore, especially the commercial mussel, Perna viridis.

Qualitative and quantitative analysis of environmental samples by laser-induced breakdown spectrometry

International Nuclear Information System (INIS)

Zorov, N B; Popov, A M; Zaytsev, S M; Labutin, T A

2015-01-01

The key achievements in the determination of trace amounts of components in environmental samples (soils, ores, natural waters, etc.) by laser-induced breakdown spectrometry are considered. Unique capabilities of this method make it suitable for rapid analysis of metals and alloys, glasses, polymers, objects of cultural heritage, archaeological and various environmental samples. The key advantages of the method that account for its high efficiency are demonstrated, in particular, a small amount of analyzed material, the absence of sample preparation, the possibility of local and remote analysis of either one or several elements. The use of chemometrics in laser-induced breakdown spectrometry for qualitative sample classification is described in detail. Various approaches to improving the figures of merit of quantitative analysis of environmental samples are discussed. The achieved limits of detection for most elements in geochemical samples are critically evaluated. The bibliography includes 302 references

Application of Neutron Activation Analysis to Geochemical Studies of Mineral Resources

Energy Technology Data Exchange (ETDEWEB)

Winchester, J. W. [Department Of Meteorology and Oceanography, University of Michigan, Ann Arbor, MI (United States); Catoggio, J. A. [Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata (Argentina)

1969-03-15

Sensitive and accurate measurement of closely related trace element concentrations in naturally occurring materials leads to the most useful geochemical information in the study of crystallizing systems. Studies of the rare earth elements have shown regularities that can be related to geological crystallization processes in igneous and sedimentary materials, and it is likely that similar studies of economic mineral deposits will lead to similar information. An analytical method should be chosen with great care to assure adequate sensitivity for the trace elements under investigation. Neutron activation analysis and spark source mass spectrometry both have high sensitivity adequate for many geochemical applications. However, simpler methods, such as atomic absorption, absorption spectrophotometry and electrochemical methods have adequate sensitivity for many elements and are preferred when suitable. (author)

Geochemical reanalysis of historical U.S. Geological Survey sediment samples from the Inmachuk, Kugruk, Kiwalik, and Koyuk River drainages, Granite Mountain, and the northern Darby Mountains, Bendeleben, Candle, Kotzebue, and Solomon quadrangles, Alaska

Science.gov (United States)

Werdon, Melanie B.; Granitto, Matthew; Azain, Jaime S.

2015-01-01

The State of Alaska’s Strategic and Critical Minerals (SCM) Assessment project, a State-funded Capital Improvement Project (CIP), is designed to evaluate Alaska’s statewide potential for SCM resources. The SCM Assessment is being implemented by the Alaska Division of Geological & Geophysical Surveys (DGGS), and involves obtaining new airborne-geophysical, geological, and geochemical data. As part of the SCM Assessment, thousands of historical geochemical samples from DGGS, U.S. Geological Survey (USGS), and U.S. Bureau of Mines archives are being reanalyzed by DGGS using modern, quantitative, geochemical-analytical methods. The objective is to update the statewide geochemical database to more clearly identify areas in Alaska with SCM potential. The USGS is also undertaking SCM-related geologic studies in Alaska through the federally funded Alaska Critical Minerals cooperative project. DGGS and USGS share the goal of evaluating Alaska’s strategic and critical minerals potential and together created a Letter of Agreement (signed December 2012) and a supplementary Technical Assistance Agreement (#14CMTAA143458) to facilitate the two agencies’ cooperative work. Under these agreements, DGGS contracted the USGS in Denver to reanalyze historical USGS sediment samples from Alaska. For this report, DGGS funded reanalysis of 653 historical USGS sediment samples from the statewide Alaska Geochemical Database Version 2.0 (AGDB2; Granitto and others, 2013). Samples were chosen from an area covering portions of the Inmachuk, Kugruk, Kiwalik, and Koyuk river drainages, Granite Mountain, and the northern Darby Mountains, located in the Bendeleben, Candle, Kotzebue, and Solomon quadrangles of eastern Seward Peninsula, Alaska (fig. 1). The USGS was responsible for sample retrieval from the National Geochemical Sample Archive (NGSA) in Denver, Colorado through the final quality assurance/quality control (QA/QC) of the geochemical analyses obtained through the USGS contract

Geochemical investigation of UMTRAP designated site at Durango, Colorado

International Nuclear Information System (INIS)

Markos, G.; Bush, K.J.

1983-09-01

This report is the result of a geochemical investigation of the former uranium mill and tailings site at Durango, Colorado. This is one in a series of site specific geochemical investigations performed on the inactive uranium mill tailings included in the UMTRA Project. The objectives of the investigation are to characterize the geochemistry, to determine the contaminant distribution resulting from the former milling activities and tailings, and to infer chemical pathways and transport mechanisms from the contaminant distribution. The results will be used to model contaminant migration and to develop criteria for long-term containment media such as a cover system which is impermeable to contaminant migration. This report assumes a familiarity with the hydrologic conditions of the site and the geochemical concepts underlying the investigation. The results reported are based on a one-time sampling of waters and solid material from the background, the area adjacent to the site, and the site. The solid samples are water extracted remove easily soluble salts and acids extracted to remove cabonates and hydroxides. The water extracts and solid samples were analyzed for the major and trace elements. A limited number of samples were analyzed for radiological components. The report includes the methods of sampling, sample processing, analysis, and data interpretation. Three major conclusions are: (1) carbonate salts and low TDS characterize the tailings; (2) the adjacent area and raffinate ponds contain contaminants deposited by a single event of fluid permeation of the soils; and (3) the Animas River adjacent to the site has elevated gross alpha activity attributed to 226 Ra in the sediments derived from the tailings or milling activities

Geochemical Constraints for Mercury's PCA-Derived Geochemical Terranes

Science.gov (United States)

Stockstill-Cahill, K. R.; Peplowski, P. N.

2018-05-01

PCA-derived geochemical terranes provide a robust, analytical means of defining these terranes using strictly geochemical inputs. Using the end members derived in this way, we are able to assess the geochemical implications for Mercury.

Leachate Geochemical Results for Ash Samples from the June 2007 Angora Wildfire Near Lake Tahoe in Northern California

Science.gov (United States)

Hageman, Philip L.; Plumlee, Geoffrey S.; Martin, Deborah A.; Hoefen, Todd M.; Adams, Monique; Lamothe, Paul J.; Todorov, Todor I.; Anthony, Michael W.

2008-01-01

This report releases leachate geochemical data for ash samples produced by the Angora wildfire that burned from June 24 to July 2, 2007, near Lake Tahoe in northern California. The leaching studies are part of a larger interdisciplinary study whose goal is to identify geochemical characteristics and properties of the ash that may adversely affect human health, water quality, air quality, animal habitat, endangered species, debris flows, and flooding hazards. The leaching study helps characterize and understand the interactions that occur when the ash comes in contact with rain or snowmelt, and helps identify the constituents that may be mobilized as run-off from these materials. Similar leaching studies were conducted on ash and burned soils from the October 2007 southern California wildfires (Hageman and others, 2008; Plumlee and others, 2007).

Geochemical orientation for mineral exploration in the Hashemite Kingdom of Jordan

Science.gov (United States)

Overstreet, W.C.; Grimes, D.J.; Seitz, J.F.

1982-01-01

This report is a supplement to previous accounts of geochemical exploration conducted in the Hashemite Kingdom of Jordan by the Natural Resources Authority of the Royal Government of Jordan and the U.S. Geological Survey. The field work on which this report is based was sponsored by the U.S. Agency for International Development, U.S. Department of State. Procedures used in collecting various kinds of rocks, ores, slags, eluvial and alluvial sediments, heavy-mineral concentrates, and organic materials for use as geochemical sample media are summarized, as are the laboratory procedures followed for the analysis of these sample materials by semiquantitative spectrographic, atomic absorption, fluorometric, and X-ray diffraction methods. Geochemical evaluations of the possibilities for economic mineral deposits in certain areas are presented. The results of these preliminary investigations open concepts for further use in geochemical exploration in the search for metallic mineral deposits in Jordan. Perhaps the most desirable new activity would be hydrogeochemical exploration for uranium and base metals, accompanied by interpretation of such remote-sensing data as results of airborne radiometric surveys and computer-enhanced LANDSAT imagery. For more conventional approaches to geochemical exploration, however, several fundamental problems regarding proper choice of geochemical sample media for different geologic and geographic parts of the Country must be solved before effective surveys can be made. The present results also show that such common geochemical exploration techniques as the determination of the trace-element contents of soils, plant ash, and slags have direct application also toward the resolution of several archaeological problems in Jordan. These include the relation of trace-elements chemistry of local soils to the composition of botanic remains, the trace-elements composition of slags to the technological development of the extractive metallurgy of

Geochemical and sedimentological signature of catastrophic saltwater inundations (tsunami), New Zealand

International Nuclear Information System (INIS)

Chague-Goff, C.; Goff, J.R.

1999-01-01

Three tidal marshes in Able Tasman National Par, New Zealand, were studied using geochemical, sedimentological and radiometric dating techniques. Charcoal and plant material samples were taken from one core in each inlet for 14 C analysis. radiocarbon ages were converted to dendrocalibrated years . All samples produced a terrestrial 13 C signal. Near surface samples were date d by measuring 137 Cs. A 1700 year record of catastrophic saltwater inundations (CSI) events (Tsunami) was produced. Up to four such events were identified, with ruptures of one or more of the Wellington, Wairarapa and Alpine Faults being the most likely tsunamigenic source. CSI signatures include: peaks in Fe and/or S, a peak in fines and contemporaneous or delayed peaks in organic content and/or loss on ignition (LOI). Geochemical data in association with grain size analyses proved to be a valuable tool in the interpretation of these events

Geochemical prospect ion results of Treinta y Tres aerial photo

International Nuclear Information System (INIS)

Zeegers, H.; Bonnefoy, D.; Garau, M.; Spangenberg, J.

1981-01-01

This report shows the geochemical prospect ion results carried out within the framework of the multielemental geochemical strategy. The samples were studied by e spectrometry in the laboratories of Orleans.

DNA-based methods of geochemical prospecting

Energy Technology Data Exchange (ETDEWEB)

Ashby, Matthew [Mill Valley, CA

2011-12-06

The present invention relates to methods for performing surveys of the genetic diversity of a population. The invention also relates to methods for performing genetic analyses of a population. The invention further relates to methods for the creation of databases comprising the survey information and the databases created by these methods. The invention also relates to methods for analyzing the information to correlate the presence of nucleic acid markers with desired parameters in a sample. These methods have application in the fields of geochemical exploration, agriculture, bioremediation, environmental analysis, clinical microbiology, forensic science and medicine.

Delineation of geochemical anomalies based on stream sediment data utilizing fractal modeling and staged factor analysis

Science.gov (United States)

Afzal, Peyman; Mirzaei, Misagh; Yousefi, Mahyar; Adib, Ahmad; Khalajmasoumi, Masoumeh; Zarifi, Afshar Zia; Foster, Patrick; Yasrebi, Amir Bijan

2016-07-01

Recognition of significant geochemical signatures and separation of geochemical anomalies from background are critical issues in interpretation of stream sediment data to define exploration targets. In this paper, we used staged factor analysis in conjunction with the concentration-number (C-N) fractal model to generate exploration targets for prospecting Cr and Fe mineralization in Balvard area, SE Iran. The results show coexistence of derived multi-element geochemical signatures of the deposit-type sought and ultramafic-mafic rocks in the NE and northern parts of the study area indicating significant chromite and iron ore prospects. In this regard, application of staged factor analysis and fractal modeling resulted in recognition of significant multi-element signatures that have a high spatial association with host lithological units of the deposit-type sought, and therefore, the generated targets are reliable for further prospecting of the deposit in the study area.

A Spatially Constrained Multi-autoencoder Approach for Multivariate Geochemical Anomaly Recognition

Science.gov (United States)

Lirong, C.; Qingfeng, G.; Renguang, Z.; Yihui, X.

2017-12-01

Separating and recognizing geochemical anomalies from the geochemical background is one of the key tasks in geochemical exploration. Many methods have been developed, such as calculating the mean ±2 standard deviation, and fractal/multifractal models. In recent years, deep autoencoder, a deep learning approach, have been used for multivariate geochemical anomaly recognition. While being able to deal with the non-normal distributions of geochemical concentrations and the non-linear relationships among them, this self-supervised learning method does not take into account the spatial heterogeneity of geochemical background and the uncertainty induced by the randomly initialized weights of neurons, leading to ineffective recognition of weak anomalies. In this paper, we introduce a spatially constrained multi-autoencoder (SCMA) approach for multivariate geochemical anomaly recognition, which includes two steps: spatial partitioning and anomaly score computation. The first step divides the study area into multiple sub-regions to segregate the geochemical background, by grouping the geochemical samples through K-means clustering, spatial filtering, and spatial constraining rules. In the second step, for each sub-region, a group of autoencoder neural networks are constructed with an identical structure but different initial weights on neurons. Each autoencoder is trained using the geochemical samples within the corresponding sub-region to learn the sub-regional geochemical background. The best autoencoder of a group is chosen as the final model for the corresponding sub-region. The anomaly score at each location can then be calculated as the euclidean distance between the observed concentrations and reconstructed concentrations of geochemical elements.The experiments using the geochemical data and Fe deposits in the southwestern Fujian province of China showed that our SCMA approach greatly improved the recognition of weak anomalies, achieving the AUC of 0.89, compared

Izu-Bonin rear-arc magmatism: Geochemical investigation of volcanoclastic material

OpenAIRE

Sæbø, Andreas

2017-01-01

Studied samples from the Izu Bonin rear arc show a distinct geochemical pattern that resemble the modern continental crust. In contrast to the volcanic front, samples from the Izu Bonin rear arc show enrichment of LREE (La, Ce, Pr, Nd) and higher K2O at a given SiO2. This suggest that processes leading up to the geochemistry observed in the rear arc is fundamental in creating the modern continental crust. Additional isotopic and trace element analysis from volcanic material rec...

Statistical interpretation of geochemical data

International Nuclear Information System (INIS)

Carambula, M.

1990-01-01

Statistical results have been obtained from a geochemical research from the following four aerial photographies Zapican, Carape, Las Canias, Alferez. They have been studied 3020 samples in total, to 22 chemical elements using plasma emission spectrometry methods.

Applications of inductively coupled plasma spectroscopy to geochemical reconnaissance for uranium exploration

International Nuclear Information System (INIS)

Cagle, G.W.; Butz, T.R.

1980-01-01

The analysis of large numbers of natural groundwater and stream sediment samples by Inductively Coupled Plasma (ICP) Spectroscopy has been applied to a geochemical reconnaissance program as part of the National Uranium Resource Evaluation Program. Approximately 25 elements have been determined in over 60,000 samples by ICP analysis. These data are combined with additional measurements obtained by atomic absorption, colorimetry, neutron activation, and fluorescence spectroscopy. Results are presented and interpreted in terms of the uranium favorability of areas in Texas where this survey has been completed

Cross-correlation analysis of 2012-2014 seismic events in Central-Northern Italy: insights from the geochemical monitoring network of Tuscany

Science.gov (United States)

Pierotti, Lisa; Facca, Gianluca; Gherardi, Fabrizio

2015-04-01

Since late 2002, a geochemical monitoring network is operating in Tuscany, Central Italy, to collect data and possibly identify geochemical anomalies that characteristically occur before regionally significant (i.e. with magnitude > 3) seismic events. The network currently consists of 6 stations located in areas already investigated in detail for their geological setting, hydrogeological and geochemical background and boundary conditions. All these stations are equipped for remote, continuous monitoring of selected physicochemical parameters (temperature, pH, redox potential, electrical conductivity), and dissolved concentrations of CO2 and CH4. Additional information are obtained through in situ discrete monitoring. Field surveys are periodically performed to guarantee maintenance and performance control of the sensors of the automatic stations, and to collect water samples for the determination of the chemical and stable isotope composition of all the springs investigated for seismic precursors. Geochemical continuous signals are numerically processed to remove outliers, monitoring errors and aseismic effects from seasonal and climatic fluctuations. The elaboration of smoothed, long-term time series (more than 200000 data available today for each station) allows for a relatively accurate definition of geochemical background values. Geochemical values out of the two-sigma relative standard deviation domain are inspected as possible indicators of physicochemical changes related to regional seismic activity. Starting on November 2011, four stations of the Tuscany network located in two separate mountainous areas of Northern Apennines separating Tuscany from Emilia-Romagna region (Equi Terme and Gallicano), and Tuscany from Emilia-Romagna and Umbria regions (Vicchio and Caprese Michelangelo), started to register anomalous values in pH and CO2 partial pressure (PCO2). Cross-correlation analysis indicates an apparent relationship between the most important seismic

Variation of heavy metals in recent sediments from Piratininga Lagoon (Brazil): interpretation of geochemical data with the aid of multivariate analysis

Science.gov (United States)

Huang, W.; Campredon, R.; Abrao, J. J.; Bernat, M.; Latouche, C.

1994-06-01

In the last decade, the Atlantic coast of south-eastern Brazil has been affected by increasing deforestation and anthropogenic effluents. Sediments in the coastal lagoons have recorded the process of such environmental change. Thirty-seven sediment samples from three cores in Piratininga Lagoon, Rio de Janeiro, were analyzed for their major components and minor element concentrations in order to examine geochemical characteristics and the depositional environment and to investigate the variation of heavy metals of environmental concern. Two multivariate analysis methods, principal component analysis and cluster analysis, were performed on the analytical data set to help visualize the sample clusters and the element associations. On the whole, the sediment samples from each core are similar and the sample clusters corresponding to the three cores are clearly separated, as a result of the different conditions of sedimentation. Some changes in the depositional environment are recognized using the results of multivariate analysis. The enrichment of Pb, Cu, and Zn in the upper parts of cores is in agreement with increasing anthropogenic influx (pollution).

Characterization of primary geochemical haloes for gold exploration at the Huanxiangwa gold deposit, China

NARCIS (Netherlands)

Wang, Changming; Carranza, E.J.M; Zhang, Shouting; Zhang, Jing; Liu, Xiaoji Liu; Zhang, Da; Sun, Xiang; Duan, Cunji

2013-01-01

Recognition of primary geochemical haloes is one of the most important tools for exploring undiscovered mineral resources. This tool is being routinely applied in exploration programs at the Huanxiangwa gold deposit, Xiong'er Mountains, China. Sampling of unweathered rock for multi-element analysis

Geochemical signature of land-based activities in Caribbean coral surface samples

Science.gov (United States)

Prouty, N.G.; Hughen, K.A.; Carilli, J.

2008-01-01

Anthropogenic threats, such as increased sedimentation, agrochemical run-off, coastal development, tourism, and overfishing, are of great concern to the Mesoamerican Caribbean Reef System (MACR). Trace metals in corals can be used to quantify and monitor the impact of these land-based activities. Surface coral samples from the MACR were investigated for trace metal signatures resulting from relative differences in water quality. Samples were analyzed at three spatial scales (colony, reef, and regional) as part of a hierarchical multi-scale survey. A primary goal of the paper is to elucidate the extrapolation of information between fine-scale variation at the colony or reef scale and broad-scale patterns at the regional scale. Of the 18 metals measured, five yielded statistical differences at the colony and/or reef scale, suggesting fine-scale spatial heterogeneity not conducive to regional interpretation. Five metals yielded a statistical difference at the regional scale with an absence of a statistical difference at either the colony or reef scale. These metals are barium (Ba), manganese (Mn), chromium (Cr), copper (Cu), and antimony (Sb). The most robust geochemical indicators of land-based activities are coral Ba and Mn concentrations, which are elevated in samples from the southern region of the Gulf of Honduras relative to those from the Turneffe Islands. These findings are consistent with the occurrence of the most significant watersheds in the MACR from southern Belize to Honduras, which contribute sediment-laden freshwater to the coastal zone primarily as a result of human alteration to the landscape (e.g., deforestation and agricultural practices). Elevated levels of Cu and Sb were found in samples from Honduras and may be linked to industrial shipping activities where copper-antimony additives are commonly used in antifouling paints. Results from this study strongly demonstrate the impact of terrestrial runoff and anthropogenic activities on coastal water

Thermogravimetric-quadrupole mass-spectrometric analysis of geochemical samples.

Science.gov (United States)

Gibson, E. K., Jr.; Johnson, S. M.

1972-01-01

Thermogravimetric-quadrupole mass-spectrometric-analysis techniques can be used to study a wide variety of problems involving decomposition processes and identification of released volatile components. A recording vacuum thermoanalyzer has been coupled with a quadrupole mass spectrometer. The rapid scan capabilities of the quadrupole mass spectrometer are used to identify the gaseous components released. The capability of the thermogravimetric-quadrupole mass spectrometer to provide analytical data for identification of the released volatile components, for determination of their sequence of release and for correlation of thermal-decomposition studies is illustrated by an analysis of the Orgueil carbonaceous chondrite.

Geochemical characteristics of Lower Jurassic source rocks in the Zhongkouzi Basin

Science.gov (United States)

Niu, Haiqing; Han, Xiaofeng; Wei, Jianshe; Zhang, Huiyuan; Wang, Baowen

2018-01-01

Zhongkouzi basin is formed in Mesozoic and Cenozoic and developed on the Hercynian folded belt, the degree of exploration for oil and gas is relatively low hitherto. In order to find out the geochemical characteristics of the source rocks and the potentials for hydrocarbon generation. The research result shows that by analysis the geochemical characteristics of outcrop samples and new core samples in Longfengshan Group, Longfengshan Group are most developed intervals of favorable source rocks. They are formed in depression period of the basin when the sedimentary environments is salt water lacustrine and the water is keeping stable; The organic matter abundance is middle-higher, the main kerogen type is II1-II2 and few samples act as III type, The organic matter maturity is low maturity to medium maturity. The organic matter maturity of the source rock from eastern part of the basin is higher than in the western region. The source rock of Longfengshan Group are in the hydrocarbon generation threshold. The great mass of source rocks are matured and in the peak stage of oil generation.

Multielement neutron activation analysis of underground water samples

International Nuclear Information System (INIS)

Kusaka, Yuzuru; Tsuji, Haruo; Fujimoto, Yuzo; Ishida, Keiko; Mamuro, Tetsuo.

1980-01-01

An instrumental neutron activation analysis by gamma-ray spectrometry with high resolution and large volume Ge (Li) detectors followed by data processing with an electronic computer was applied to the multielemental analysis to elucidate the chemical qualities of the underground water which has been widely used in the sake brewing industries in Mikage, Uozaki and Nishinomiya districts, called as miyamizu. The evaporated residues of the water samples were subjected to the neutron irradiations in reactor for 1 min at a thermal flux of 1.5 x 10 12 n.cm -2 .sec -1 and for 30 hrs at a thermal flux of 9.3 x 10 11 n.cm -2 .sec -1 or for 5 hrs at a thermal flux of 3.9 x 10 12 n.cm -2 .sec -1 . Thus, 11 elements in the former short irradiation and 38 elements in the latter two kinds of long irradiation can be analyzed. Conventional chemical analysis including atomic absorption method and others are also applied on the same samples, and putting the all results together, some considerations concerning the geochemical meaning of the analytical values are made. (author)

Predictive geochemical mapping using environmental correlation

International Nuclear Information System (INIS)

Wilford, John; Caritat, Patrice de; Bui, Elisabeth

2016-01-01

The distribution of chemical elements at and near the Earth's surface, the so-called critical zone, is complex and reflects the geochemistry and mineralogy of the original substrate modified by environmental factors that include physical, chemical and biological processes over time. Geochemical data typically is illustrated in the form of plan view maps or vertical cross-sections, where the composition of regolith, soil, bedrock or any other material is represented. These are primarily point observations that frequently are interpolated to produce rasters of element distributions. Here we propose the application of environmental or covariate regression modelling to predict and better understand the controls on major and trace element geochemistry within the regolith. Available environmental covariate datasets (raster or vector) representing factors influencing regolith or soil composition are intersected with the geochemical point data in a spatial statistical correlation model to develop a system of multiple linear correlations. The spatial resolution of the environmental covariates, which typically is much finer (e.g. ∼90 m pixel) than that of geochemical surveys (e.g. 1 sample per 10-10,000 km 2 ), carries over to the predictions. Therefore the derived predictive models of element concentrations take the form of continuous geochemical landscape representations that are potentially much more informative than geostatistical interpolations. Environmental correlation is applied to the Sir Samuel 1:250,000 scale map sheet in Western Australia to produce distribution models of individual elements describing the geochemical composition of the regolith and exposed bedrock. As an example we model the distribution of two elements – chromium and sodium. We show that the environmental correlation approach generates high resolution predictive maps that are statistically more accurate and effective than ordinary kriging and inverse distance weighting interpolation

Baseline geochemical data for stream sediment and surface water samples from Panther Creek, the Middle Fork of the Salmon River, and the Main Salmon River from North Fork to Corn Creek, collected prior to the severe wildfires of 2000 in central Idaho

Science.gov (United States)

Eppinger, Robert G.; Briggs, Paul H.; Brown, Zoe Ann; Crock, James G.; Meier, Allen; Theodorakos, Peter M.; Wilson, Stephen A.

2001-01-01

In 1996, the U.S. Geological Survey conducted a reconnaissance baseline geochemical study in central Idaho. The purpose of the baseline study was to establish a 'geochemical snapshot' of the area, as a datum for monitoring future change in the geochemical landscape, whether natural or human-induced. This report presents the methology, analytical results, and sample descriptions for water, sediment, and heavy-mineral concentrate samples collected during this geochemical investigation. In the summer of 2000, the Clear Creek, Little Pistol, and Shellrock wildfires swept across much of the area that was sampled. Thus, these data represent a pre-fire baseline geochemical dataset. A 2001 post- fire study is planned and will involve re-sampling of the pre-fire baseline sites, to allow for pre- and post-fire comparison.

Radioactive waste isolation in salt: peer review of the Office of Nuclear Waste Isolation's Geochemical Program Plan

International Nuclear Information System (INIS)

Harrison, W.; Seitz, M.; Fenster, D.; Lerman, A.; Brookins, D.; Tisue, M.

1984-02-01

Describe the management program for coordinating subcontractors and their work, and integrating research results. Appropriate flowcharts should be included. Provide more information on the overall scope of the program. For each subcontractor, provide specific workscopes that indicate whether analytical activities are developmental or routine, approximate number of analyses to be made, and something of the adequacy of the analyses to meet program goals. Indicate interfaces with other earth-science disciplines like hydrology and with other groups doing relevant geochemical research and engineering design. Address the priorities for each activity or group of activities. High priority should be given to early development of a geochemical statement of what constitutes suitable salt for a repository. Reference standard procedures for sampling, sample preservation, and sample analysis wherever appropriate or, if not appropriate, indicate that any deviations from standard procedures will be documented. Ensure that appropriate quality assurance procedures will be followed for the procedures listed above. Include specific procedures for the choice, verification, validation, and documentation of computer codes related to the geochemical aspects of repository performance assessment. Include activities addressing regional hydrochemistry and make clear that each principal hydrogeologic unit at each site will be studied geochemically. Indicate that proposed plans for obtaining hydrogeochemical data will be included in each site characterization plan. Describe how site geochemical stability will be handled, especially with respect to dissolution, postemplacement geochemistry, human influences, and climatic variations. Minor recommendations and suggested improvements in the text of the plan are given in Sec. 5

[Recent advances in analysis of petroleum geological samples by comprehensive two-dimensional gas chromatography].

Science.gov (United States)

Gao, Xuanbo; Chang, Zhenyang; Dai, Wei; Tong, Ting; Zhang, Wanfeng; He, Sheng; Zhu, Shukui

2014-10-01

Abundant geochemical information can be acquired by analyzing the chemical compositions of petroleum geological samples. The information obtained from the analysis provides scientifical evidences for petroleum exploration. However, these samples are complicated and can be easily influenced by physical (e. g. evaporation, emulsification, natural dispersion, dissolution and sorption), chemical (photodegradation) and biological (mainly microbial degradation) weathering processes. Therefore, it is very difficult to analyze the petroleum geological samples and they cannot be effectively separated by traditional gas chromatography/mass spectrometry. A newly developed separation technique, comprehensive two-dimensional gas chromatography (GC x GC), has unique advantages in complex sample analysis, and recently it has been applied to petroleum geological samples. This article mainly reviews the research progres- ses in the last five years, the main problems and the future research about GC x GC applied in the area of petroleum geology.

Measuring Sulfur Isotope Ratios from Solid Samples with the Sample Analysis at Mars Instrument and the Effects of Dead Time Corrections

Science.gov (United States)

Franz, H. B.; Mahaffy, P. R.; Kasprzak, W.; Lyness, E.; Raaen, E.

2011-01-01

The Sample Analysis at Mars (SAM) instrument suite comprises the largest science payload on the Mars Science Laboratory (MSL) "Curiosity" rover. SAM will perform chemical and isotopic analysis of volatile compounds from atmospheric and solid samples to address questions pertaining to habitability and geochemical processes on Mars. Sulfur is a key element of interest in this regard, as sulfur compounds have been detected on the Martian surface by both in situ and remote sensing techniques. Their chemical and isotopic composition can belp constrain environmental conditions and mechanisms at the time of formation. A previous study examined the capability of the SAM quadrupole mass spectrometer (QMS) to determine sulfur isotope ratios of SO2 gas from a statistical perspective. Here we discuss the development of a method for determining sulfur isotope ratios with the QMS by sampling SO2 generated from heating of solid sulfate samples in SAM's pyrolysis oven. This analysis, which was performed with the SAM breadboard system, also required development of a novel treatment of the QMS dead time to accommodate the characteristics of an aging detector.

Geochemical features of the elemental composition of meadowsweet (Filipendula ulmaria (L).Maxim) in Kemerovo Oblast

Science.gov (United States)

Zhdanov, V. A.; Sobolev, I. S.; Baranovskaya, N. V.; Kolesnikova, E. A.; Chernenkaya, E. V.; Yalaltdinova, A. R.

2016-09-01

Biogeochemical sampling of the aboveground part of meadowsweet (Fillipendula Ulmaria (L). Maxim) allowed us to study ecological and geochemical features of 10 regions in Kemerovo Oblast, including both natural and man-made landscapes. The content of 55 elements in the plant is determined by ICP-MS. Statistical analysis of the results allowed us to establish the effect of the soil mineral composition and the mining region specificity on the elemental composition of meadowsweet, to reveal significant positive correlations of the elements and to establish a statistically significant difference in the studied areas on the basis of the content of some elements. Sample reference to one of the clusters, followed by an assessment of their geochemical features is determined by the K-average method.

Analysis of the geochemical gradient created by surface-groundwater interactions within riverbanks of the East River in Crested Butte, Colorado

Science.gov (United States)

Lunzer, J.; Williams, K. H.; Malenda, H. F.; Nararne-Sitchler, A.

2016-12-01

An improved understanding of the geochemical gradient created by the mixing of surface and groundwater of a river system will have considerable impact on our understanding of microorganisms, organic cycling and biogeochemical processes within these zones. In this study, the geochemical gradient in the hyporheic zone is described using a variety of geochemical properties. A system of shallow groundwater wells were installed in a series of transects along a stream bank. Each transect consists of several wells that progress away from the river bank in a perpendicular fashion. From these wells, temperature, conductivity and pH of water samples were obtained via hand pumping or bailing. These data show a clear geochemical gradient that displays a distinct zone in the subsurface where the geochemical conditions change from surface water dominated to groundwater dominated. For this study, the East River near Crested Butte, Colorado has been selected as the river of interest due the river being a relatively undisturbed floodplain. Additionally, the specific section chosen on the East River displays relatively high sinuosity meaning that these meandering sections will produce hyporheic zones that are more laterally expansive than what would be expected on a river of lower sinuosity. This increase in lateral extension of the hyporheic zone will make depicting the subtle changes in the geochemical gradient much easier than that of a river system in which the hyporheic zone is not as laterally extensive. Data has been and will be continued to be collected at different river discharges to evaluate the geochemical gradient at differing rates. Overall, this characterization of the geochemical gradient along stream banks will produce results that will aid in the further use of geochemical methods to classify and understand hyporheic exchange zones and the potential expansion of these techniques to river systems of differing geologic and geographic conditions.

Use of partial dissolution techniques in geochemical exploration

Science.gov (United States)

Chao, T.T.

1984-01-01

Application of partial dissolution techniques to geochemical exploration has advanced from an early empirical approach to an approach based on sound geochemical principles. This advance assures a prominent future position for the use of these techniques in geochemical exploration for concealed mineral deposits. Partial dissolution techniques are classified as single dissolution or sequential multiple dissolution depending on the number of steps taken in the procedure, or as "nonselective" extraction and as "selective" extraction in terms of the relative specificity of the extraction. The choice of dissolution techniques for use in geochemical exploration is dictated by the geology of the area, the type and degree of weathering, and the expected chemical forms of the ore and of the pathfinding elements. Case histories have illustrated many instances where partial dissolution techniques exhibit advantages over conventional methods of chemical analysis used in geochemical exploration. ?? 1984.

Lithology and mineralogy recognition from geochemical logging tool data using multivariate statistical analysis.

Science.gov (United States)

Konaté, Ahmed Amara; Ma, Huolin; Pan, Heping; Qin, Zhen; Ahmed, Hafizullah Abba; Dembele, N'dji Dit Jacques

2017-10-01

The availability of a deep well that penetrates deep into the Ultra High Pressure (UHP) metamorphic rocks is unusual and consequently offers a unique chance to study the metamorphic rocks. One such borehole is located in the southern part of Donghai County in the Sulu UHP metamorphic belt of Eastern China, from the Chinese Continental Scientific Drilling Main hole. This study reports the results obtained from the analysis of oxide log data. A geochemical logging tool provides in situ, gamma ray spectroscopy measurements of major and trace elements in the borehole. Dry weight percent oxide concentration logs obtained for this study were SiO 2 , K 2 O, TiO 2 , H 2 O, CO 2 , Na 2 O, Fe 2 O 3 , FeO, CaO, MnO, MgO, P 2 O 5 and Al 2 O 3 . Cross plot and Principal Component Analysis methods were applied for lithology characterization and mineralogy description respectively. Cross plot analysis allows lithological variations to be characterized. Principal Component Analysis shows that the oxide logs can be summarized by two components related to the feldspar and hydrous minerals. This study has shown that geochemical logging tool data is accurate and adequate to be tremendously useful in UHP metamorphic rocks analysis. Copyright © 2017 Elsevier Ltd. All rights reserved.

Mars Geochemical Instrument (MarGI): An instrument for the analysis of the Martian surface and the search for evidence of life

Science.gov (United States)

Kojiro, Daniel R.; Mancinelli, Rocco; Martin, Joe; Holland, Paul M.; Stimac, Robert M.; Kaye, William J.

2005-01-01

The Mars Geochemical Instrument, MarGI, was developed to provide a comprehensive analysis of the rocks and surface material on Mars. The instrument combines Differential Thermal Analysis (DTA) with miniature Gas Chromatography-Ion Mobility Spectrometry (GC-IMS) to identify minerals, the presence and state of water, and organic compounds. Miniature pyrolysis ovens are used to both, conduct DTA analysis of soil or crushed rocks samples, and pyrolyze the samples at temperatures up to 1000 degrees C for GC-IMS analysis of the released gases. This combination of analytical processes and techniques, which can characterize the mineralogy of the rocks and soil, and identify and quantify volatiles released during pyrolysis, has applications across a wide range of target sites including comets, planets, asteroids, and moons such as Titan and Europa. The MarGI analytical approach evolved from the Cometary Ice and Dust Experiment (CIDEX) selected to fly on the Comet Rendezvous Asteroid Flyby Mission (CRAF).

Geochemical investigation of UMTRAP designated site at Salt Lake City, Utah

International Nuclear Information System (INIS)

Markos, G.; Bush, K.J.

1983-09-01

This report is the result of a geochemical investigation of the former uranium mill and tailings site at Salt Lake City, Utah. This is one in a series of site specific geochemical investigations performed on the inactive uranium mill tailings included in the Uranium Mill Tailings Remedial Action Project. The objectives of the investigation are to characterize the geochemistry, to determine the contaminant distribution resulting from the former milling activities and tailings, and to infer chemical pathways and transport mechanisms from the contaminant distribution. The results will be used to model contaminant migration and to develop criteria for long-term containment media such as a cover system which is impermeable to contaminant migration. This report assumes a familiarity with the hydrologic conditions of the site and the geochemical concepts underlying the investigation. The results reported are based on a one-time sampling of waters and solid material from the background, the area adjacent to the site, and the site. The solid samples were water extracted to remove easily soluble salts and acid extracted to remove carbonates and hydroxides. The water extracts and solid samples were anlyzed for the major and trace elements. The report includes the methods of sampling, sample processing, analysis, and data interpretation. Four major conclusions are: (1) sediments in the ditches and creeks adjacent to the site contain tailings, however, the waters were generally not contaminated; (2) tailings are mixed with the soils within a meter below the tailings in some locations, however, water-soluble contaminants decrease to below background levels within 30 cm below the tailings; (3) there has not been significant acid seepage into the soils below the tailings; and (4) salt crusts on the tailings contain trace elements, with the elements that form chloride complexes having the greatest accumulation

Chemical analysis of geological samples

International Nuclear Information System (INIS)

Malhotra, R.K.

1997-01-01

Most of the analytical methodology used in geochemical exploration has been based on molecular absorption, atomic absorption, and ICP-AES, ICPMAS etc. Detection limit and precision are factors in the choice of methodology in search of metallic ores and are related to the accuracy of data. A brief outline of the various chemical analysis techniques explaining essentially the basics of measurement principles and instrumentation is discussed

Manual hierarchical clustering of regional geochemical data using a Bayesian finite mixture model

International Nuclear Information System (INIS)

Ellefsen, Karl J.; Smith, David B.

2016-01-01

Interpretation of regional scale, multivariate geochemical data is aided by a statistical technique called “clustering.” We investigate a particular clustering procedure by applying it to geochemical data collected in the State of Colorado, United States of America. The clustering procedure partitions the field samples for the entire survey area into two clusters. The field samples in each cluster are partitioned again to create two subclusters, and so on. This manual procedure generates a hierarchy of clusters, and the different levels of the hierarchy show geochemical and geological processes occurring at different spatial scales. Although there are many different clustering methods, we use Bayesian finite mixture modeling with two probability distributions, which yields two clusters. The model parameters are estimated with Hamiltonian Monte Carlo sampling of the posterior probability density function, which usually has multiple modes. Each mode has its own set of model parameters; each set is checked to ensure that it is consistent both with the data and with independent geologic knowledge. The set of model parameters that is most consistent with the independent geologic knowledge is selected for detailed interpretation and partitioning of the field samples. - Highlights: • We evaluate a clustering procedure by applying it to geochemical data. • The procedure generates a hierarchy of clusters. • Different levels of the hierarchy show geochemical processes at different spatial scales. • The clustering method is Bayesian finite mixture modeling. • Model parameters are estimated with Hamiltonian Monte Carlo sampling.

Petrographic and geochemical characteristics of the Cypress Creek salt core

International Nuclear Information System (INIS)

1983-07-01

Law Engineering Testing Company supervised the drilling of a corehole into the stock of Cypress Creek Dome, located in Perry County, Mississippi. A total of 170 ft of caprock and 501 ft of salt stock was recovered for physical examination and chemical analysis. This report describes the types of analyses performed and summarizes the data developed. The entire caprock and salt core were described and photographed prior to selection of samples for petrologic and geochemical analysis. Transmitted light techniques were used to determine gross structural and compositional variations in the core. The core lithologies are presented graphically, at a scale of 1 in. to 2 ft. In addition to the detailed field descriptions and photographs, petrologic studies performed on selected caprock and salt samples included: thin-section examination, scanning-electron microscope studies, energy-dispersion analysis, and x-ray-diffraction analysis. Geochemical analyses were performed to determine the average elemental composition of the salt core and amounts of methane and carbon dioxide gases contained within the salt grains. Except for two thin (3 and 6 ft thick) gypsum zones in the top 27 ft of the caprock, the core is predominantly anhydrite (generally 80%). Minor amounts of dolomite and calcite are also present. The salt core consists predominantly of crystalline halite, fine- to medium-grained (0.25 to 1 in.) with few megacrysts. Anhydrite occurs in the salt core as disseminated grains, ranging in length from <0.1 in. to 12 in. Discrete zones exist within the salt core, distinguished from one another primarily by the character of the anhydrite inclusions

Geochemical mapping of Anheung, Wonju and Eomjeong sheets (1:50,000)

Energy Technology Data Exchange (ETDEWEB)

Lee, Jin Soo; Seo, Hyo Joon; Shin, Seong Cheon; Chi, Se Jung; Kim, Seong Jae [Korea Inst. of Geology Mining and Materials, Taejon (Korea, Republic of)

1995-12-01

A geochemical mapping was undertaken on the three quadrangles of the Anheung, Wonju and Eomjeong sheets (1:50,000, new edition) in the southwestern Taebaeg Mineralized Belt. The survey area, ca. 1,900 km{sup 2}, is covered mostly by Jurassic granites and Precambrian metamorphic rocks, and partly by Cambro-Ordovician limestones and the Cretaceous igneous and sedimentary rocks. Light mineral stream sediments and water samples, totally 751 for each media, were collected from active channels of primary or secondary order with a mean sampling density of 1/2.4 km{sup 2}. Geochemical maps were made on 17 elements (i.e., Ag, Al, As, Ba, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Sr, V, W, Zn) for stream sediments. Geochemical distribution maps for water samples were independently made on major and minor components (i.e., Na, K, Li, Si, Ca, Mg, Al, As, B, Ba, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Sr, V, Zn, F{sup -}, Cl{sup -}, NO{sub 3}{sup -}, NO{sub 2}{sup -}, PO{sub 4}{sup 3-}, SO{sub 4}{sup 2-}, HCO{sub 3}{sup -}) and other physico-chemical properties (i.e., Electric Conductivity, Total Dissolved Solids, pH, Dissolved Oxygen). Analysis was carried out by Ion Coupled Plasma Spectrometry and Ion Chromatography. Geochemical anomalies were evaluated based upon geological and other field information. The Ag-As, Cu-Pb-Zn and W-Mo anomalies of stream sediments in the northern Anheung and southern Eomjeong sheets indicate a contamination derived from mining districts. Pb-Zn anomalies from southeastern area in the Eomjeong sheet may suggest a potential of polymetallic deposits near Mesozoic granites intruding the Ogcheon strata. High concentrations of Ca, Na, K, Cl{sup -} and NO{sub 3}{sup -} in stream waters around Chungju and Wonju imply a strong pollution over urban districts and stock farms. (author). 57 refs., 70 figs.

Geochemical prospecting for Cu mineralization in an arid terrain-central Iran

Science.gov (United States)

Mokhtari, Ahmad Reza; Roshani Rodsari, Parisa; Fatehi, Moslem; Shahrestani, Shahed; Pournik, Peyman

2014-12-01

Geochemical sampling and data processing were implemented for prospecting Cu mineralization through catchment basin approach in central Iran, Yazd province, over drainage systems in order to determine areas of interest for the detailed exploration program. The target zone, inside an area called Kalout-e-Ashrafa in Yazd province-Iran, was characterized by the collection of 107 stream sediment samples. Catchment basin modeling was conducted based on digital elevation model (DEM) and geological map of the study area. Samples were studied by univariate and multivariate statistical techniques of exploratory data analysis, classical statistical analysis and cluster analysis. The results showed that only Cu had anomalous behavior and it did not exhibit a considerable correlation with other elements. Geochemical maps were prepared for Cu and anomalous zones and separated for potential copper mineralization. It was concluded that due to especial geomorphological and geographical characteristics (smooth topography, negligible annual precipitation and insufficient thickness of silicified Cu-bearing outcrops of the area), low concentrations of Cu would be expected for the delineation of promising zones in similar trains. Using cluster analysis showed that there was a strong correlation between Ag, Sr and S. Calcium and Pb present moderate correlation with Cu. Additionally, there was a strong correlation between Zn and Li, thereby indicating a meaningful correlation with Fe, P, Ti and Mg. Aluminum, Sc and V had a correlation with Be and K. Applying threshold value according to MAD (median absolute deviation) helped us to distinguish anomalous catchments more properly. Finally, there was a significant kind of conformity among anomalous catchment basins and silicified veins and veinlets (as validating index) at the central part of the area.

Geochemical wolframite fingerprinting - the likelihood ratio approach for laser ablation ICP-MS data.

Science.gov (United States)

Martyna, Agnieszka; Gäbler, Hans-Eike; Bahr, Andreas; Zadora, Grzegorz

2018-05-01

Wolframite has been specified as a 'conflict mineral' by a U.S. Government Act, which obliges companies that use these minerals to report their origin. Minerals originating from conflict regions in the Democratic Republic of the Congo shall be excluded from the market as their illegal mining, trading, and taxation are supposed to fuel ongoing violent conflicts. The German Federal Institute for Geosciences and Natural Resources (BGR) developed a geochemical fingerprinting method for wolframite based on laser ablation inductively coupled plasma-mass spectrometry. Concentrations of 46 elements in about 5300 wolframite grains from 64 mines were determined. The issue of verifying the declared origins of the wolframite samples may be framed as a forensic problem by considering two contrasting hypotheses: the examined sample and a sample collected from the declared mine originate from the same mine (H 1 ), and the two samples come from different mines (H 2 ). The solution is found using the likelihood ratio (LR) theory. On account of the multidimensionality, the lack of normal distribution of data within each sample, and the huge within-sample dispersion in relation to the dispersion between samples, the classic LR models had to be modified. Robust principal component analysis and linear discriminant analysis were used to characterize samples. The similarity of two samples was expressed by Kolmogorov-Smirnov distances, which were interpreted in view of H 1 and H 2 hypotheses within the LR framework. The performance of the models, controlled by the levels of incorrect responses and the empirical cross entropy, demonstrated that the proposed LR models are successful in verifying the authenticity of the wolframite samples. Graphical abstract Geochemical wolframite fingerprinting.

Geochemical Parameters Required from the SKB Site Characterisation Programme

International Nuclear Information System (INIS)

Bath, Adrian

2002-01-01

SKB has described its approach to site characterisation in a number of Technical Reports. One of the scientific topics in which specific information requirements and priorities are set out is geochemistry. This report for SKI examines critically whether the geochemical parameters identified in the SKB programme documents will be adequate for safety and regulatory requirements. It also examines some of the details of parameter requirements and interpretation tools that will be necessary to convert site investigation data into knowledge about chemical conditions and groundwater movements. The SKB strategy for geochemical data focuses on a small number of 'suitability indicators', primarily dissolved oxygen, pH and salinity. Their parameter requirements aim to assess those primary characteristics, as well as to acquire a wider range of data that will support those assessments and provide a broader understanding of candidate areas. An initial observation in this review that, though it is a primary suitability indicator, dissolved oxygen apparently will not be measured and instead will be inferred from other redox indicators. This raises a number of issues about sampling and monitoring measures, analytical data reliability and sensitivity, and the degree of confidence in geochemical understanding. A geochemical programme involves reconnaissance by desk study and acquisition of new data at levels of details that are appropriate to the stage of site investigations. As early as possible, a conceptual model of a candidate area should help to define the objectives of geochemical measurements on both rock and groundwater samples. It is recommended that parameters requirements should be defined and considered not only in terms of isolated measurements but more in terms of addressing broader objectives that relate to safety and also to geoscientific understanding. The safety priorities remain (e.g. dissolved oxygen) but will then be supported by an understanding of processes

Geochemical Parameters Required from the SKB Site Characterisation Programme

Energy Technology Data Exchange (ETDEWEB)

Bath, Adrian [Intellisci Ltd., Loughborough (United Kingdom)

2002-01-01

SKB has described its approach to site characterisation in a number of Technical Reports. One of the scientific topics in which specific information requirements and priorities are set out is geochemistry. This report for SKI examines critically whether the geochemical parameters identified in the SKB programme documents will be adequate for safety and regulatory requirements. It also examines some of the details of parameter requirements and interpretation tools that will be necessary to convert site investigation data into knowledge about chemical conditions and groundwater movements. The SKB strategy for geochemical data focuses on a small number of 'suitability indicators', primarily dissolved oxygen, pH and salinity. Their parameter requirements aim to assess those primary characteristics, as well as to acquire a wider range of data that will support those assessments and provide a broader understanding of candidate areas. An initial observation in this review that, though it is a primary suitability indicator, dissolved oxygen apparently will not be measured and instead will be inferred from other redox indicators. This raises a number of issues about sampling and monitoring measures, analytical data reliability and sensitivity, and the degree of confidence in geochemical understanding. A geochemical programme involves reconnaissance by desk study and acquisition of new data at levels of details that are appropriate to the stage of site investigations. As early as possible, a conceptual model of a candidate area should help to define the objectives of geochemical measurements on both rock and groundwater samples. It is recommended that parameters requirements should be defined and considered not only in terms of isolated measurements but more in terms of addressing broader objectives that relate to safety and also to geoscientific understanding. The safety priorities remain (e.g. dissolved oxygen) but will then be supported by an understanding of

Coastal Aquifer Contamination and Geochemical Processes Evaluation in Tugela Catchment, South Africa—Geochemical and Statistical Approaches

Directory of Open Access Journals (Sweden)

Badana Ntanganedzeni

2018-05-01

Full Text Available Assessment of groundwater quality, contamination sources and geochemical processes in the coastal aquifer of Tugela Catchment, South Africa were carried out by the geochemical and statistical approach using major ion chemistry of 36 groundwater samples. Results suggest that the spatial distribution pattern of EC, TDS, Na, Mg, Cl and SO4 are homogenous and elevated concentrations are observed in the wells in the coastal region and few wells near the Tugela River. Wells located far from the coast are enriched by Ca, HCO3 and CO3. Durov diagrams, Gibbs plots, ionic ratios, chloro alkaline indices (CAI1 and CAI2 and correlation analysis imply that groundwater chemistry in the coastal aquifer of Tugela Catchment is regulated by the ion exchange, mineral dissolution, saline sources, and wastewater infiltration from domestic sewage; septic tank leakage and irrigation return flow. Principle component analysis also ensured the role of saline and anthropogenic sources and carbonates dissolution on water chemistry. Spatial distributions of factor score also justify the above predictions. Groundwater suitability assessment indicates that around 80% and 90% of wells exceeded the drinking water standards recommended by the WHO and South African drinking water standards (SAWQG, respectively. Based on SAR, RSC, PI, and MH classifications, most of the wells are suitable for irrigation in the study region. USSL classification suggests that groundwater is suitable for coarse-textured soils and salt-tolerant crops. The study recommends that a proper management plan is required to protect this coastal aquifer efficiently.

Geochemical characteristics of peat from two raised bogs of Germany

Science.gov (United States)

Mezhibor, A. M.

2016-11-01

Peat has a wide range of applications in different spheres of human activity, and this is a reason for a comprehensive study. This research represents the results of an ICP-MS study of moss and peat samples from two raised bogs of Germany. Because of the wide use of sphagnum moss and peat, determining their geochemical characteristics is an important issue. According to the results obtained, we can resume that the moss samples from Germany are rich in Cu, As, Y, Zr, Nb, and REE. The geochemical composition of the bogs reflects the regional environmental features and anthropogenic influence.

A national-scale geochemical and mineralogical survey of soils of the conterminous United States

International Nuclear Information System (INIS)

Smith, David B.; Cannon, William F.; Woodruff, Laurel G.

2011-01-01

Highlights: → Sampling for national-scale soil geochemical and mineralogical survey completed for conterminous USA. → Natural variation for most elements is approximately three orders of magnitude. → Composition of soil parent material is the major controlling factor. → Climate (average annual precipitation) is also an important controlling factor for some elements. → Sample archive (4800 sites) available for future investigations. - Abstract: In 2007, the US Geological Survey initiated a low-density (1 site per 1600 km 2 , c. 4800 sites) geochemical and mineralogical survey of soils of the conterminous USA. The ideal sampling protocol at each site includes a sample from 0-5 cm depth, a composite of the soil A horizon, and a sample from the soil C horizon. The 3 , HClO 4 and HF. Separate methods are used for As, Hg, Se and total C on this same size fraction. The major mineralogical components are determined by a quantitative X-ray diffraction method. Sampling was completed in 2010 with chemical and mineralogical analysis currently underway. Preliminary results for a swath from the central USA to Florida clearly show the effects of soil parent material and climate on the chemical and mineralogical composition of soils. A sample archive will be established and made available for future investigations.

Remote Raman - laser induced breakdown spectroscopy (LIBS) geochemical investigation under Venus atmospheric conditions

Energy Technology Data Exchange (ETDEWEB)

Clegg, Sanuel M [Los Alamos National Laboratory; Barefield, James E [Los Alamos National Laboratory; Humphries, Seth D [Los Alamos National Laboratory; Wiens, Roger C [Los Alamos National Laboratory; Vaniman, D. T. [Los Alamos National Laboratory; Sharma, S. K. [UNIV OF HAWAII; Misra, A. K. [UNIV OF HAWAII; Dyar, M. D. [MT. HOLYOKE COLLEGE; Smrekar, S. E. [JET PROPULSION LAB.

2010-12-13

The extreme Venus surface temperatures ({approx}740 K) and atmospheric pressures ({approx}93 atm) create a challenging environment for surface missions. Scientific investigations capable of Venus geochemical observations must be completed within hours of landing before the lander will be overcome by the harsh atmosphere. A combined remote Raman - LIBS (Laser Induced Breakdown Spectroscopy) instrument is capable of accomplishing the geochemical science goals without the risks associated with collecting samples and bringing them into the lander. Wiens et al. and Sharma et al. demonstrated that both analytical techniques can be integrated into a single instrument capable of planetary missions. The focus of this paper is to explore the capability to probe geologic samples with Raman - LIBS and demonstrate quantitative analysis under Venus surface conditions. Raman and LIBS are highly complementary analytical techniques capable of detecting both the mineralogical and geochemical composition of Venus surface materials. These techniques have the potential to profoundly increase our knowledge of the Venus surface composition, which is currently limited to geochemical data from Soviet Venera and VEGA landers that collectively suggest a surface composition that is primarily tholeiitic basaltic with some potentially more evolved compositions and, in some locations, K-rich trachyandesite. These landers were not equipped to probe the surface mineralogy as can be accomplished with Raman spectroscopy. Based on the observed compositional differences and recognizing the imprecise nature of the existing data, 15 samples were chosen to constitute a Venus-analog suite for this study, including five basalts, two each of andesites, dacites, and sulfates, and single samples of a foidite, trachyandesite, rhyolite, and basaltic trachyandesite under Venus conditions. LIBS data reduction involved generating a partial least squares (PLS) model with a subset of the rock powder standards to

Gamma Spectrometric Determination of U, Th, K and Some Geochemical Applications

International Nuclear Information System (INIS)

Dodona, A.; Tashko, A.

2001-01-01

The application of 'in situ' gamma-spectrometric method (''infinite'' environment), made possible the simultanious determination of U, Th and K. 4 channel gamma-spectrometric analyser with NaI(TI) scintilation counter crystal detector (103 cm 3 φ=50x50mm) was used to determin U, Th(more than 1-2 ppm) and K (more than 1%) in laboratory conditions. The detector was inserted into a lead camera and calibrated for measurement geometry with vessel of ''Marineli'' type of a 17o cm 3 volume. The study of main factors, which influence in the gamma spectrometric measurements, (the technical, physical, geometrical and time parameters) has been carried out. International standards of U, Th, K and internal monitoring standard samples are used for the calibration. External analytical control has been realized by other radiometric and chemical methods. The detection limits ( 1 ppm Th, 2ppm U and 1% K) and the relative errors (17-20% for 1-10 ppm U, Th and 10-15% for more than 10 ppm U, Th and more than 1% K) guarantee a quantitative analysis that may be used successfully in the geochemical studies. Some geochemical applications, based on the content of Th, U and Th/U ratio in rocks samples that we have we have analyzed with this method, are shown in this paper. U, Th and their ratio are used as trace elements to indicate the differences between the acidic magmatic rocks of Albania (Th/U ratio=2-6 and>10). The bimodal character of Th/U scattering in ignimbrides and monzonites (Korabi zone) shows that in addition to the ''normal'' rocks, there are also some ones enriched with Th, So, the differential analysis of Th, U, and K may be used as geochemical exploration criteria for the radioactive and non-radioactive mineralization, such as REE (Rare Earth Elements), phospghorites, bauxites, placers etc. (authors)

Orientation geochemical survey for uranium exploration using 230Th

International Nuclear Information System (INIS)

Xia Dingliang.

1985-01-01

The distribution of 230 Th in soils, rocks and ores and its relationship with respect to uranium ore formation are discussed for its possible use in geochemical exploration for U. 230 Th, U and Ra, being members of the same decay series, are different in their geochemical behavior upon which the study is orientated. Twenty uranium deposits and occurrences located in western and southern Hunan province are tested. Geochemical data obtained are comprehensively correlated. It is suggested that 230 Th is useful not only in U-Ra disequilibrium study but also in understanding the geochemical evolution of U ores. The data aid to interpret the genesis of uranium deposits and to assess the radioactive anomalies and uranium-bearing zones. Therefore, it can be adopted as a tool for searching in deep-buried uranium ores. The field procedure is rather simple and flexible to meet any geological environment. It is easy to read out and is less influnced by any kind of interference. In case of disequilibrium caused by oxidation and reduction during the period of ore formation it still gives good indication compared with that of radiometry, radonmetry and geochemical sampling for U

Geochemical characterization of Parana Basin volcanic rocks: petrogenetic implications

International Nuclear Information System (INIS)

Marques, L.S.

1988-01-01

A detailed study of the geochemical characteristics of Parana Basin volcanic rocks is presented. The results are based on the analyses of major and trace elements of 158 samples. Ninety three of these volcanic samples belong to 8 flow sequences from Rio Grande do Sul and Santa Catarina States. The remaining sixty five samples are distributed over the entire basin. In order to study the influence of crustal contamination processes in changing chemical characteristics of the volcanic rocks, 47 samples representative of the crystalline basement of the southern and southeastern Parana Basin were also analysed. Several petrogenetic models were tested to explain the compocional variability of the volcanic rocks, in particular those of southern region. The results obtained sugest an assimilation-fractional crystallization process as viable to explain the differences of both the chemical characteristics and Sr isotope initial ratios observed in basic and intermediate rocks. A model involving melting processes of basic material, trapped at the base of the crust, with composition similar to low and high TiO 2 basalts appears to be a possibility to originate the Palmas and Chapeco acid melts, respectively. The study of ''uncontaminated'' or poorly contaminated low TiO 2 basic rocks from the southern, central and northern regions shows the existence of significant differences in the geochemical charactetistics according to their geographical occurrence. A similar geochemical diversity is also observed in high TiO 2 basalts and Chapeco volcanics. Differences in incompatible element ratios between low and high TiO 2 ''uncontaminated'' or poorly contaminated basalts suggest that they could have been produced by different degrees of melting in a garnet peridotite source. Geochemical and isotopic (Sr and Nd) data also support the view that basalts from northern and southern regions of Parana Basin originated from mantle source with different composition. (author) [pt

Review of geochemical measurement techniques for a nuclear waste repository in bedded salt

International Nuclear Information System (INIS)

Knauss, K.G.; Steinborn, T.L.

1980-01-01

A broad, general review is presented of geochemical measurement techniques that can provide data necessary for site selection and repository effectiveness assessment for a radioactive waste repository in bedded salt. The available measurement techniques are organized according to the parameter measured. The list of geochemical parameters include all those measurable geochemical properties of a sample whole values determine the geochemical characteristics or behavior of the system. For each technique, remarks are made pertaining to the operating principles of the measurement instrument and the purpose for which the technique is used. Attention is drawn to areas where further research and development are needed

Site study plan for geochemical analytical requirements and methodologies: Revision 1

International Nuclear Information System (INIS)

1987-12-01

This site study plan documents the analytical methodologies and procedures that will be used to analyze geochemically the rock and fluid samples collected during Site Characterization. Information relating to the quality aspects of these analyses is also provided, where available. Most of the proposed analytical procedures have been used previously on the program and are sufficiently sensitive to yield high-quality analyses. In a few cases improvements in analytical methodology (e.g., greater sensitivity, fewer interferences) are desired. Suggested improvements to these methodologies are discussed. In most cases these method-development activities have already been initiated. The primary source of rock and fluid samples for geochemical analysis during Site Characterization will be the drilling program, as described in various SRP Site Study Plans. The Salt Repository Project (SRP) Networks specify the schedule under which the program will operate. Drilling will not begin until after site ground water baseline conditions have been established. The Technical Field Services Contractor (TFSC) is responsible for conducting the field program of drilling and testing. Samples and data will be handled and reported in accordance with established SRP procedures. A quality assurance program will be utilized to assure that activities affecting quality are performed correctly and that the appropriate documentation is maintained. 28 refs., 9 figs., 14 tabs

Determination and interpretation of environmental water samples contaminated by uranium mining activities

International Nuclear Information System (INIS)

Meinrath, G.; Volke, P.; Helling, C.; Merkel, B.J.; Dudel, E.G.

1999-01-01

Interpretation of environmental behavior of uranium is based on several steps of data analysis and statistical inference. First step is sampling and analyzing of uranium in field samples by routine laboratory methods. Such methods have to fulfill multiple requirements like robustness, efficiency, low detection limit and precision. A comparison of different approaches in assigning uncertainty to experimentally obtained analytical data shows that classical error estimation is not significantly inferior to more sophisticated modern techniques like inverse regression or orthogonal regression. A second step is the correlation of analytical data with current state of insight into environmental behavior of uranium. Such a correlation furthers the choice of adequate geochemical models and quality of geochemical data base for subsequent detailed analysis, e.g. by geochemical modeling. An appraisal of the individual steps in this complex analysis is given on the basis of statistical procedures for calibration and an E H -pH diagram of uranium for atmospheric conditions. (orig.)

Multielement geochemical reconnaissance for uranium in the Palmyrides region of central Syria

International Nuclear Information System (INIS)

Jubeli, Y.M.; Hale, M.

1988-01-01

Multielement reconnaissance geochemistry coupled with ground scintillation gamma ray measurements has been used to investigate the dispersion patterns of uranium and other major and trace elements in the arid Palmyrides region of central Syria. Over 500 geochemical samples of outcropping rock, wadi and playa sediments, overburden and groundwaters were taken over an area of approximately 9000 sq km. Most samples were analyzed for 25 major and trace elements by nebulization ICPAES; for As, Sb, Bi and Se by hydride generation and ICPAES; and for U, Th and La and other REE by neutron activation analysis. The resulting data were interpreted with the aid of univariate and multivariate statistical methods. The areal distributions of U, its associated elements, multivariate geochemical functions and factor scores were mapped using computer graphics. Results of the factor analysis indicate that the primary lithogeochemical dispersion patterns of uranium and associated elements are controlled by a combination of structural, lithological and environmental factors. Uranium and associated elements have subsequently been leached out of the phosphorite and other U enriched clayey limestones and carbonate rocks into the hydro- geologic regime. Redistribution of these elements is taking place along fracture zones and major faults. A degree of urnaium accumulation in a Neogene aquifer of the Ad-Daww basin is evident

UMTRA Project water sampling and analysis plan, Gunnison, Colorado: Revision 1

International Nuclear Information System (INIS)

1994-11-01

This water sampling and analysis plan summarizes the results of previous water sampling activities and the plan for future water sampling activities, in accordance with the Guidance Document for Preparing Sampling and Analysis Plans for UMTRA Sites. A buffer zone monitoring plan for the Dos Rios Subdivision is included as an appendix. The buffer zone monitoring plan was developed to ensure continued protection to the public from residual contamination. The buffer zone is beyond the area depicted as contaminated ground water due to former milling operations. Surface remedial action at the Gunnison Uranium Mill Tailings Remedial Action Project site began in 1992; completion is expected in 1995. Ground water and surface water will be sampled semiannually at the Gunnison processing site and disposal site. Results of previous water sampling at the Gunnison processing site indicate that ground water in the alluvium is contaminated by the former uranium processing activities. Background ground water conditions have been established in the uppermost aquifer at the Gunnison disposal site. The monitor well locations provide a representative distribution of sampling points to characterize ground water quality and ground water flow conditions in the vicinity of the sites. The list of analytes has been modified with time to reflect constituents that are related to uranium processing activities and the parameters needed for geochemical evaluation

Statistical characterization of a large geochemical database and effect of sample size

Science.gov (United States)

Zhang, C.; Manheim, F.T.; Hinde, J.; Grossman, J.N.

2005-01-01

The authors investigated statistical distributions for concentrations of chemical elements from the National Geochemical Survey (NGS) database of the U.S. Geological Survey. At the time of this study, the NGS data set encompasses 48,544 stream sediment and soil samples from the conterminous United States analyzed by ICP-AES following a 4-acid near-total digestion. This report includes 27 elements: Al, Ca, Fe, K, Mg, Na, P, Ti, Ba, Ce, Co, Cr, Cu, Ga, La, Li, Mn, Nb, Nd, Ni, Pb, Sc, Sr, Th, V, Y and Zn. The goal and challenge for the statistical overview was to delineate chemical distributions in a complex, heterogeneous data set spanning a large geographic range (the conterminous United States), and many different geological provinces and rock types. After declustering to create a uniform spatial sample distribution with 16,511 samples, histograms and quantile-quantile (Q-Q) plots were employed to delineate subpopulations that have coherent chemical and mineral affinities. Probability groupings are discerned by changes in slope (kinks) on the plots. Major rock-forming elements, e.g., Al, Ca, K and Na, tend to display linear segments on normal Q-Q plots. These segments can commonly be linked to petrologic or mineralogical associations. For example, linear segments on K and Na plots reflect dilution of clay minerals by quartz sand (low in K and Na). Minor and trace element relationships are best displayed on lognormal Q-Q plots. These sensitively reflect discrete relationships in subpopulations within the wide range of the data. For example, small but distinctly log-linear subpopulations for Pb, Cu, Zn and Ag are interpreted to represent ore-grade enrichment of naturally occurring minerals such as sulfides. None of the 27 chemical elements could pass the test for either normal or lognormal distribution on the declustered data set. Part of the reasons relate to the presence of mixtures of subpopulations and outliers. Random samples of the data set with successively

Geochemical exploration for uranium

International Nuclear Information System (INIS)

1988-01-01

This Technical Report is designed mainly to introduce the methods and techniques of uranium geochemical exploration to exploration geologists who may not have had experience with geochemical exploration methods in their uranium programmes. The methods presented have been widely used in the uranium exploration industry for more than two decades. The intention has not been to produce an exhaustive, detailed manual, although detailed instructions are given for a field and laboratory data recording scheme and a satisfactory analytical method for the geochemical determination of uranium. Rather, the intention has been to introduce the concepts and methods of uranium exploration geochemistry in sufficient detail to guide the user in their effective use. Readers are advised to consult general references on geochemical exploration to increase their understanding of geochemical techniques for uranium

Petrologic and geochemical characterization of the Bullfrog Member of the Crater Flat Tuff: outcrop samples used in waste package experiments

International Nuclear Information System (INIS)

Knauss, K.G.

1983-09-01

In support of the Waste Package Task within the Nevada Nuclear Waste Storage Investigation (NNWSI), experiments on hydrothermal rock/water interaction, corrosion, thermomechanics, and geochemical modeling calculations are being conducted. All of these activities require characterization of the initial bulk composition, mineralogy, and individual phase geochemistry of the potential repository host rock. This report summarizes the characterization done on samples of the Bullfrog Member of the Crater Flat Tuff (Tcfb) used for Waste Package experimental programs. 11 references, 17 figures, 3 tables

Drowning in Geochemical Data: The Good, the bad, and the Ugly

Science.gov (United States)

Hofmann, A. W.; Goldstein, S. L.

2008-12-01

Geochemical databases are placing unprecedented amounts of geochemical data at the fingertips of professionals and students. How these data are being used is taking an increasingly important role in shaping our thinking about the Earth. Databases have helped to expose (and eventually kill?) some long- cherished myths, such as the idea of the well-homogenized upper-mantle reservoir, and and they have made geochemical data accessible to geophysicists and enabled them to look at geochemistry with fresh eyes, leading to genuinely new insights. Yet, their very accessibility also makes them "dangerous tools" in the hands of the inexperienced. Statistical treatment of masses of geochemical data without, or with excessive, filtering can yield all sorts of "answers" we would probably be better off without. Data that are severely flawed (due to alteration or poor analytical quality, errors in published data, or errors during data entry) might not be easily identified by, say, a geodynamicist. Other dangers stem from overrepresentation of over-sampled locations and the general, but faulty, assumption of random sampling of the Earth. We will show examples where raw downloads of data from databases without extensive screening can yield data collections where the garbage swamps the useful information. We will also show impressive but meaningless correlations, e.g. upper-mantle temperature versus atmospheric temperature. The lesson is that screening is necessary. On the other hand, sound database compilations now demonstrate that average incompatible-element concentrations in global MORB are two to five times higher than published estimates. This fundamentally changes 30-year-old geochemical mass balance estimates of the mantle. OIBs are fundamentally similar to MORBs but are isotopically shifted, on average, to more "enriched" values. Mantle geochemistry is now fully consistent with dynamic models of "whole-mantle" circulation, with the likely exception of a relatively small

X-Ray and Radiometrics in Geo-Ecological and Geochemical Mapping

Energy Technology Data Exchange (ETDEWEB)

Fedyanin, S. N. [Navoi Mining and Metallurgical Combinat (Uzbekistan)

2014-05-15

Monitoring of tailing pits of uranium ore conversion products and reserve supplies of low-grade ores stored in dumps is traditionally based on radiation environment on these sites and adjacent territories. The results of gamma-ray spectrometry of solid fractions and radon concentration measurement in liquid and gas phases of technogenic formations are used in radiation hazard evaluation. Radiometric testing practice of low-activity field formations in loose and lump masses shows that due to high emanating ability it is necessary to use dual-channel radiometer for ionizing radiation background record and compensation. Thus gamma-radiometry is not the direct method of uranium content determination and alfa- and beta-radiometry can be correctly used only for sample analysis in laboratory environment. Consequently, distant express testing with the help of X-ray radiometric (XRM) instruments (on calcium, iron, manganese, titanium, copper, arsenic, lead, strontium, selenium, molybdenum, uranium, etc.) is recommended for additional introduction in field observations of radio-ecological environment in mining and processing production tailing and dumps of low-grade ore reserve supplies. Thanks to preliminary areal schemes of geochemical zonality as per XRM data XRM application allows to use the sample limit, given for a wide range of laboratory analyses rationally. Sampling places and their number as well as kinds of laboratory analyses are chosen based on XRM data.It is rather effective to use laboratory variant of atomic absorptive analysis on mercury and stibium in gases (GA), generated in the process of grated samples calcination in muffle furnaces. During the presentation of the report In order to prove the effectiveness of XRM and GA presentation graphics with the results of areal mapping using the above methods and geochemical testing on the territories of Tashkent (Uzbekistan) and Chimkent (Kazakhstan) regions within the framework of the geological and ecological

The geochemical profile of Mn, Co, Cu and Fe in Kerteh Mangrove Forest, Terengganu

International Nuclear Information System (INIS)

Kamaruzzaman, B.Y.; Antotina, A.; Airiza, Z.; Syalindran, S.; Ong, M.C.

2007-01-01

The geochemical profile of Kerteh mangrove sediments was analyzed for the vertical and horizontal distribution. The 100 cm core sediment sample and 15 surface sediments samples were taken from the field. The geochemical elements of Mn, Co, Cu and Fe of the sediments were analyzed. Geochemical proxy of Mn, Co, Cu and Fe were analyzed by using Inductively Coupled Plasma-Mass Spectrometry (ICP-MS). The mean concentrations of Mn, Co, Cu and Fe for the vertical distribution were 210.18 μg/ g, 15.55 μg/ g, 43.65 μg/ g and 1.88 μg/ g respectively. on the other hand, the mean concentrations of the geochemical elements for horizontal distributions were 230.50 μg/ g for Mn, 17.57 μg/ g for Co, 43.381 μg/ g for Cu and 2.93 μg/ g for Fe. Enrichment factor and normalization was used to point out the level of pollution. The EF and the normalization indicated that all the geochemical elements were from the natural sources. (author)

History and progress of the North American Soil Geochemical Landscapes Project, 2001-2010

Science.gov (United States)

Smith, David B.; Cannon, William F.; Woodruff, Laurel G.; Rivera, Francisco Moreira; Rencz, Andrew N.; Garrett, Robert G.

2012-01-01

In 2007, the U.S. Geological Survey, the Geological Survey of Canada, and the Mexican Geological Survey initiated a low-density (1 site per 1600 km2, 13323 sites) geochemical and mineralogical survey of North American soils (North American Soil Geochemical Landscapes Project). Sampling and analytical protocols were developed at a series of workshops in 20032004 and pilot studies were conducted from 20042007. The ideal sampling protocol at each site includes a sample from 05 cm depth, a composite of the soil A horizon, and a sample from the soil C horizon. The 3, HClO4, and HF. Separate methods are used for As, Hg, Se, and total C on this same size fraction. The major mineralogical components are determined by a quantitative X-ray diffraction method. Sampling in the conterminous U.S. was completed in 2010 (c. 4800 sites) with chemical and mineralogical analysis currently underway. In Mexico, approximately 66% of the sampling (871 sites) had been done by the end of 2010 with completion expected in 2012. After completing sampling in the Maritime provinces and portions of other provinces (472 sites, 7.6% of the total), Canada withdrew from the project in 2010. Preliminary results for a swath from the central U.S. to Florida clearly show the effects of soil parent material and climate on the chemical and mineralogical composition of soils. A sample archive will be established and made available for future investigations.

Determination of geochemical distribution of platinum elements in chromites and related minerals using neutron activation analysis technique

International Nuclear Information System (INIS)

Agiorgitis, G.

1978-08-01

Results of Pt, Pd, Ir, Os and Ru determination in various rocks and minerals using radiochemical neutron activation method are presented and geochemical correlations of the platinum elements studied. The method of analysis was described in detail in 4 progress reports

Geochemical modelling: what phenomena are missing

International Nuclear Information System (INIS)

Jacquier, P.

1989-12-01

In the framework of safety assessment of radioactive waste disposal, retention phenomena are usually taken into account by the Kd concept. It is well recognized that this concept is not enough for safety assessment models, because of the several and strong assumptions which are involved in this kind of representation. One way to have a better representation of the retention phenomena, is to substitute for this Kd concept an explicit description of geochemical phenomena and then couple transport codes with geochemical codes in a fully or a two-step procedure. We use currently such codes, but the scope of this paper is to display the limits today of the geochemical modelling in connection with sites analysis for deep disposal. In this paper, we intend to give an overview of phenomena which are missing in the geochemical models, or which are not completely introduced in the models. We can distinguish, on one hand phenomena for which modelling concepts exist such as adsorption/desorption and, on the other hand, phenomena for which modelling concepts do not exist for the moment such as colloids, and complexation by polyelectrolyte solutions (organics). Moreover we have to take care of very low concentrations of radionuclides, which can be expected from the leaching processes in the repository. Under those conditions, some reactions may not occur. After a critical review of the involved phenomena, we intend to stress the main directions of the wishful evolution of the geochemical modelling. This evolution should improve substantially the quality of the above-mentioned site assessments

Soil Iodine Determination in Deccan Syneclise, India: Implications for Near Surface Geochemical Hydrocarbon Prospecting

International Nuclear Information System (INIS)

Mani, Devleena; Kumar, T. Satish; Rasheed, M. A.; Patil, D. J.; Dayal, A. M.; Rao, T. Gnaneshwar; Balaram, V.

2011-01-01

The association of iodine with organic matter in sedimentary basins is well documented. High iodine concentration in soils overlying oil and gas fields and areas with hydrocarbon microseepage has been observed and used as a geochemical exploratory tool for hydrocarbons in a few studies. In this study, we measure iodine concentration in soil samples collected from parts of Deccan Syneclise in the west central India to investigate its potential application as a geochemical indicator for hydrocarbons. The Deccan Syneclise consists of rifted depositional sites with Gondwana–Mesozoic sediments up to 3.5 km concealed under the Deccan Traps and is considered prospective for hydrocarbons. The concentration of iodine in soil samples is determined using ICP-MS and the values range between 1.1 and 19.3 ppm. High iodine values are characteristic of the northern part of the sampled region. The total organic carbon (TOC) content of the soil samples range between 0.1 and 1.3%. The TOC correlates poorly with the soil iodine (r 2 < 1), indicating a lack of association of iodine with the surficial organic matter and the possibility of interaction between the seeping hydrocarbons and soil iodine. Further, the distribution pattern of iodine compares well with two surface geochemical indicators: the adsorbed light gaseous hydrocarbons (methane through butane) and the propane-oxidizing bacterial populations in the soil. The integration of geochemical observations show the occurrence of elevated values in the northern part of the study area, which is also coincident with the presence of exposed dyke swarms that probably serve as conduits for hydrocarbon microseepage. The corroboration of iodine with existing geological, geophysical, and geochemical data suggests its efficacy as one of the potential tool in surface geochemical exploration of hydrocarbons. Our study supports Deccan Syneclise to be promising in terms of its hydrocarbon prospects.

Geochemical studies of potential source minerals of radon: case studies in Hungary

Energy Technology Data Exchange (ETDEWEB)

Rajnai, G.; Nagy-Balogh, J.; Gal-Solymos, K.; Konc, Z.; Breitner, D.; Barabas, A.; Szabo, C. [Eotvos Univ., Lithosphere Fluid Research Lab, Dept. of Petrology and Geochemistry, Budapest (Hungary); Barabas, A. [Eotvos Univ., Dept. of Geophysics, Budapest (Hungary)

2006-07-01

In Hungary, during the past decade five distinct regions have been chosen to find possible explanations of the uncommonly high radon background radiation values. The main aim of the research is to study U- and Th-bearing minerals in petrographic and geochemical characters. Besides the microscopic techniques, whole rock and in situ geochemical analytical methods were applied to determine the bulk U and Th content of the studied geological samples. We assume that some of the radon measured is related to the U and Th contents of the samples. (authors)

Utilization of Neutron Activation Analysis for geochemical study of major and trace elements in Bouregreg river basin (Morocco)

International Nuclear Information System (INIS)

Bounouira, H.; Bounakhla, M.; Embarch, K.; Choukri, A.; Cherkaoui, R.; Gaudry, A.; Treuil, M.; Chakiri, S.

2010-01-01

The Bouregreg river basin is located in the moroccan central massif which consists mainly of palaeozoic formations that were subject to the Hercynian orogeny. This study documents the backround geochemistry and hydrochemistry of the Bouregreg river basin, focusing on the distribution of major and trace elements, Rock samples were collected at 9 locations along the bouregreg river and its tributaries in the winter of 2005. Major (Al, fe, Mn, Na, K and Ti) and trace (Rb, Cs, Sr, Sc, Ba, Cr, V, Co, Ni, Zn, As, Sb, La, Ce, Nd, Sm, Tb, Dy, Yb, Lu, Hf, Ta, Mo, Th and U) elements were anlysed using instrumental Neutron Activation Analysis (INAA). Data show that most of the geochemistry and hydrochemistry are related to regional and local geology. the geochemical heritage of geological environment in the Bouregreg river basin is very important, that results from the more compatible behaviour and the inertia of some elements during the weathering (3d transition elements (Co, Ni, Cr,...), interne transition elements f (lanthanides, Zr, Hf, Nb, Ta,...)). The geochemical homogeneity of the basin shows also heritage during the crustal accretion (magmatism-metamorphism-sedimention) and the typology of this continental area is the same that the Upper Continental Crust (UCC). Some anomalously high heavy metal analyses, particulary for As and Sb, may be related to anthropogenic activities

The role of atomic absorption spectrometry in geochemical exploration

Science.gov (United States)

Viets, J.G.; O'Leary, R. M.

1992-01-01

In this paper we briefly describe the principles of atomic absorption spectrometry (AAS) and the basic hardware components necessary to make measurements of analyte concentrations. Then we discuss a variety of methods that have been developed for the introduction of analyte atoms into the light path of the spectrophotometer. This section deals with sample digestion, elimination of interferences, and optimum production of ground-state atoms, all critical considerations when choosing an AAS method. Other critical considerations are cost, speed, simplicity, precision, and applicability of the method to the wide range of materials sampled in geochemical exploration. We cannot attempt to review all of the AAS methods developed for geological materials but instead will restrict our discussion to some of those appropriate for geochemical exploration. Our background and familiarity are reflected in the methods we discuss, and we have no doubt overlooked many good methods. Our discussion should therefore be considered a starting point in finding the right method for the problem, rather than the end of the search. Finally, we discuss the future of AAS relative to other instrumental techniques and the promising new directions for AAS in geochemical exploration. ?? 1992.

Stream-sediment geochemical exploration for uranium in Narigan area Central Iran

International Nuclear Information System (INIS)

Yazdi, M.; Khoshnoodi, K.; Kavand, M.; Ashteyani, A. R.

2009-01-01

Uranium deposits of Iran occur mainly in the Central Iran zone. Several uranium deposits have been discovered in this zone. The Narigan area is one of the most important uranium mineralized area in this zone. The uranium bearing sequences in this area are contained in the plutonic to volcanic rocks of Narigan which intruded to the Pre-Cambrian pyroclastics rocks. Plutonic and volcanic rocks are granite, rhyolite and volcanoclastic. Diabasic dykes have been intruded to these igneous rocks. The plutonic and volcanic rocks have been covered by Cretaceous limestones which seem to be youngest the rocks in this area. The aim of our project is to develop a regional exploration strategy for uranium in these igneous rocks. A grid-based sampling was planned following the results of the previous geochemical mapping at a scale of 1:100,000, integrated with geophysical data and alteration zones and outcrop of intrusive rocks. The following results are based on geological, and stream geochemical explorations in 1:20000 scale of this area. During this study 121 samples were collected from the stream sediments of <80 mesh for final sampling. Ten percent of the samples were used for checking laboratories errors. The samples were collected according to conventional methods from 30-40 cm depth of stream sediments. Finally, geochemical and radiometric data were combined and the results introduced 3 anomalies in the Narigan area

Geochemical fractionation of 210Pb in oxic estuarine sediments of Coatzacoalcos River, Gulf of Mexico

International Nuclear Information System (INIS)

Ontiveros-Cuadras, J.F.; Ruiz-Fernandez, A.C.; Perez-Bernal, L.H.; Sanchez-Cabeza, J.A.; Universitat Autonoma de Barcelona; Wee-Kwong, L.L.

2012-01-01

210 Pb activities were analyzed in surface sediments from the Coatzacoalcos River (Gulf of Mexico) to evaluate its distribution according to sediment grain size and in different geochemical compartments by using sequential extraction techniques. The geochemical fractionation experiments provided compatible results: by using the Tessier's method more than 90% of the 210 Pb activity in the samples was found the residual fraction (primary and secondary minerals) and the remaining ( 210 Pb content was found in comparative amounts in the reactive, the silicate, and the pyrite fractions (accounting together for >80%), and the rest was found in the residual fraction. The grain size fractionation analyses showed that the 210 Pb activities were mostly retained in the clay fraction, accounting up to 60-70% of the 210 Pb total activity in the sediment sample and therefore, it is concluded that the separation of the clay fraction can be useful to improve the analysis of low 210 Pb content sediments for dating purposes. (author)

Geochemical dispersion of Si, Al, Fe, Mn, Na, K, Cu and Zn elements in soils and their use for characterization areas geochemically homogeneous

International Nuclear Information System (INIS)

Silva, W.R.L. da.

1982-01-01

Variations in the chemical composition of soils are used to characterize sub-areas geochemically - homogenous. The application of this methodology in a tropical humid region of accentuated topography constitute the principal objective of the present research. Samples of red latosols (Horizon B) developed over granite, sandstone and basalt occurring in the Central Granite Region of the Serra dos Carajas, Para State, Brazil were analized for the elements Si, Al, Fe, Mn, Na, K, Cu e Zn, by atomic absorption spectrophotometry. Based on the criterion of similarity in the chemical composition (Cluster Analysis, Factor Analysis) the soils were separeted in to different groups. The geographical distribution of the different groups permit the establishment of a close relationship between the different parent lithologies and their corresponding soils. (author)

Relationship of oil seep in Kudat Peninsula with surrounding rocks based on geochemical analysis

Science.gov (United States)

Izzati Azman, Nurul; Nur Fathiyah Jamaludin, Siti

2017-10-01

This study aims to investigate the relation of oil seepage at Sikuati area with the structural and petroleum system of Kudat Peninsula. The abundance of highly carbonaceous rocks with presence of lamination in the Sikuati Member outcrop at Kudat Peninsula may give an idea on the presence of oil seepage in this area. A detailed geochemical analysis of source rock sample and oil seepage from Sikuati area was carried out for their characterization and correlation. Hydrocarbon propectivity of Sikuati Member source rock is poor to good with Total Organic Carbon (TOC) value of 0.11% to 1.48%. and also categorized as immature to early mature oil window with Vitrinite Reflectance (VRo) value of 0.43% to 0.50 %Ro. Based on biomarker distribution, from Gas Chromatography (GC) and Gas Chromatography-Mass Spectrometry (GC-MS) analysis, source rock sample shows Pr/Ph, CPI and WI of 2.22 to 2.68, 2.17 to 2.19 and 2.46 to 2.74 respectively indicates the source rock is immature and coming from terrestrial environment. The source rock might be rich in carbonaceous material organic matter resulting from planktonic/bacterial activity which occurs at fluvial to fluvio-deltaic environment. Overall, the source rock from outcrop level of Kudat Peninsula is moderately prolific in term of prospectivity and maturity. However, as go far deeper beneath the surface, we can expect more activity of mature source rock that generate and expulse hydrocarbon from the subsurface then migrating through deep-seated fault beneath the Sikuati area.

Adjustment of geochemical background by robust multivariate statistics

Science.gov (United States)

Zhou, D.

1985-01-01

Conventional analyses of exploration geochemical data assume that the background is a constant or slowly changing value, equivalent to a plane or a smoothly curved surface. However, it is better to regard the geochemical background as a rugged surface, varying with changes in geology and environment. This rugged surface can be estimated from observed geological, geochemical and environmental properties by using multivariate statistics. A method of background adjustment was developed and applied to groundwater and stream sediment reconnaissance data collected from the Hot Springs Quadrangle, South Dakota, as part of the National Uranium Resource Evaluation (NURE) program. Source-rock lithology appears to be a dominant factor controlling the chemical composition of groundwater or stream sediments. The most efficacious adjustment procedure is to regress uranium concentration on selected geochemical and environmental variables for each lithologic unit, and then to delineate anomalies by a common threshold set as a multiple of the standard deviation of the combined residuals. Robust versions of regression and RQ-mode principal components analysis techniques were used rather than ordinary techniques to guard against distortion caused by outliers Anomalies delineated by this background adjustment procedure correspond with uranium prospects much better than do anomalies delineated by conventional procedures. The procedure should be applicable to geochemical exploration at different scales for other metals. ?? 1985.

Uruguay Mining inventory. Florida fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H.; Artignan, D.; Vairon, P.

1982-01-01

This work is about the geochemical prospecting carried out in Florida fotoplano within the framework of Uruguay Mining inventory. In this work were covered 660 km2 obtaining 752 samples for study which were analyzed by Plasma Emission Spectrometry in Orleans BRGM laboratories

Geochemical Investigations of Groundwater Stability

International Nuclear Information System (INIS)

Bath, Adrian

2006-05-01

palaeohydrogeological conditions. It is likely that inland areas have had longer durations of post-glacial fresh water infiltration than coastal areas, possibly causing greater degrees of dilution and dispersion of preexisting groundwaters and thus overprinting their hydrochemical and isotopic 'fingerprints'. Lower post-glacial hydraulic gradients relative to inland sites may account for the occurrence of more relict cold-climate water at coastal sites. Some general observations are based on rather thin evidence and therefore speculative. Firstly, it seems that glacial melt water penetrated many hundreds of metres and in some places to at least 1,000 m depth. However the low remaining proportions of melt water and of much older saline Shield water suggest that melt water flux did not fully displace pre-existing groundwaters at these depths. Secondly, where there has been post-glacial infiltration of palaeo-Baltic sea water, the density stratification or compartmentalisation effect coupled with low hydraulic gradient has reduced rates of subsequent fresh water circulation after shoreline recession. There are many uncertainties in interpreting these geochemical indicators in terms of the penetration depths of glacial melt waters and the degree to which they replace preexisting groundwaters, of other aspects of groundwater stability, and of comparisons between inland and coastal groundwater systems. Uncertainties derive partly from the reliability of groundwater samples as being representative of in situ conditions, and partly from the non-uniqueness of interpretative models. Future investigations using these approaches need to improve sampling, to make conjunctive use of geochemical and isotopic indicators which have varying timescales and sensitivities, and to integrate these indicators with palaeohydrogeological modelling to support the development of reliable groundwater flow and solute transport models for Performance Assessment

A geostatistical method applied to the geochemical study of the Chichinautzin Volcanic Field in Mexico

Science.gov (United States)

Robidoux, P.; Roberge, J.; Urbina Oviedo, C. A.

2011-12-01

The origin of magmatism and the role of the subducted Coco's Plate in the Chichinautzin volcanic field (CVF), Mexico is still a subject of debate. It has been established that mafic magmas of alkali type (subduction) and calc-alkali type (OIB) are produced in the CVF and both groups cannot be related by simple fractional crystallization. Therefore, many geochemical studies have been done, and many models have been proposed. The main goal of the work present here is to provide a new tool for the visualization and interpretation of geochemical data using geostatistics and geospatial analysis techniques. It contains a complete geodatabase built from referred samples over the 2500 km2 area of CVF and its neighbour stratovolcanoes (Popocatepetl, Iztaccihuatl and Nevado de Toluca). From this database, map of different geochemical markers were done to visualise geochemical signature in a geographical manner, to test the statistic distribution with a cartographic technique and highlight any spatial correlations. The distribution and regionalization of the geochemical signatures can be viewed in a two-dimensional space using a specific spatial analysis tools from a Geographic Information System (GIS). The model of spatial distribution is tested with Linear Decrease (LD) and Inverse Distance Weight (IDW) interpolation technique because they best represent the geostatistical characteristics of the geodatabase. We found that ratio of Ba/Nb, Nb/Ta, Th/Nb show first order tendency, which means visible spatial variation over a large scale area. Monogenetic volcanoes in the center of the CVF have distinct values compare to those of the Popocatepetl-Iztaccihuatl polygenetic complex which are spatially well defined. Inside the Valley of Mexico, a large quantity of monogenetic cone in the eastern portion of CVF has ratios similar to the Iztaccihuatl and Popocatepetl complex. Other ratios like alkalis vs SiO2, V/Ti, La/Yb, Zr/Y show different spatial tendencies. In that case, second

Establishing geochemical background levels of selected trace elements in areas having geochemical anomalies: The case study of the Orbetello lagoon (Tuscany, Italy)

International Nuclear Information System (INIS)

Romano, Elena; Bergamin, Luisa; Croudace, Ian W.; Ausili, Antonella; Maggi, Chiara; Gabellini, Massimo

2015-01-01

The determination of background concentration values (BGVs) in areas, characterised by the presence of natural geochemical anomalies and anthropogenic impact, appears essential for a correct pollution assessment. For this purpose, it is necessary to establish a reliable method for determination of local BGVs. The case of the Orbetello lagoon, a geologically complex area characterized by Tertiary volcanism, is illustrated. The vertical concentration profiles of As, Cd, Cr, Cu, Hg, Ni, Pb and Zn were studied in four sediment cores. Local BGVs were determined considering exclusively samples not affected by anthropogenic influence, recognized by means of multivariate statistics and radiochronological dating ( 137 Cs and 210 Pb). Results showed BGVs well-comparable with mean crustal or shale values for most of the considered elements except for Hg (0.87 mg/kg d.w.) and As (16.87 mg/kg d.w.), due to mineralization present in the catchment basin draining into the lagoon. - Highlights: • Pollution assessment in areas with geochemical anomalies needs local reference values. • A new method for the determination of background values (BGV) was established. • Geochemical data from unpolluted samples of sediment cores were used. • Statistics and geochronology were applied to recognize unpolluted sediments. • Anthropogenically influenced samples were not considered for BGV determination. - A method including multivariate statistics and radiochronological dating is proposed for determining local background values for trace elements using analytical data form sediment cores

Geochemical mapping using stream sediments in west-central Nigeria: Implications for environmental studies and mineral exploration in West Africa

International Nuclear Information System (INIS)

Lapworth, Dan J.; Knights, Katherine V.; Key, Roger M.; Johnson, Christopher C.; Ayoade, Emmanuel; Adekanmi, Michael A.; Arisekola, Tunde M.; Okunlola, Olugbenga A.; Backman, Birgitta; Eklund, Mikael; Everett, Paul A.; Lister, Robert T.; Ridgway, John; Watts, Michael J.; Kemp, Simon J.; Pitfield, Peter E.J.

2012-01-01

This paper provides an overview of regional geochemical mapping using stream sediments from central and south-western Nigeria. A total of 1569 stream sediment samples were collected and 54 major and trace elements determined by ICP-MS and Au, Pd and Pt by fire assay. Multivariate statistical techniques (e.g., correlation analysis and principal factor analysis) were used to explore the data, following appropriate data transformation, to understand the data structure, investigate underlying processes controlling spatial geochemical variability and identify element associations. Major geochemical variations are controlled by source geology and provenance, as well as chemical weathering and winnowing processes, more subtle variations are a result of land use and contamination from anthropogenic activity. This work has identified placer deposits of potential economic importance for Au, REE, Ta, Nb, U and Pt, as well as other primary metal deposits. Areas of higher As and Cr (>2 mg/kg and >70 mg/kg respectively) are associated with Mesozoic and younger coastal sediments in SW Nigeria. High stream sediment Zr concentrations (mean >0.2%), from proximal zircons derived from weathering of basement rocks, have important implications for sample preparation and subsequent analysis due to interferences. Associated heavy minerals enriched in high field strength elements, and notably rare earths, may also have important implications for understanding magmatic processes within the basement terrain of West Africa. This study provides important new background/baseline geochemical values for common geological domains in Nigeria (which extend across other parts of West Africa) for assessment of contamination from urban/industrial land use changes and mining activities. Regional stream sediment mapping is also able to provide important new information with applications across a number of sectors including agriculture, health, land use and planning.

Analysis on geochemical conditions of uranium mineralization in Bashibulake uranium deposit, Xinjiang

International Nuclear Information System (INIS)

Liu Zhangyue; Dong Wenming; Cai Genqing; Liu Hongxu; Deng Huabo

2011-01-01

By studying the palaeoclimate and metallogenesis related geochemical indexes, this paper proposes that the hosting rocks should form in geochemical oxidation setting under arid palaeoclimate. The study on element assemblage associated with uranium mineralization indicates that the target hosting rocks suffered from different degrees of reworking of reducing fluid at first and then being superimposed by supergene oxidative fluid at tectonic uplifting stage. The uranium mineralization is located in reworked and superimposed places of two types of fluid. (authors)

UMTRA project water sampling and analysis plan, Gunnison, Colorado

International Nuclear Information System (INIS)

1994-06-01

This water sampling and analysis plan summarizes the results of previous water sampling activities and the plan for water sampling activities for calendar year 1994. A buffer zone monitoring plan is included as an appendix. The buffer zone monitoring plan is designed to protect the public from residual contamination that entered the ground water as a result of former milling operations. Surface remedial action at the Gunnison Uranium Mill Tailings Remedial Action Project site began in 1992; completion is expected in 1995. Ground water and surface water will be sampled semiannually in 1994 at the Gunnison processing site (GUN-01) and disposal site (GUN-08). Results of previous water sampling at the Gunnison processing site indicate that ground water in the alluvium is contaminated by the former uranium processing activities. Background ground water conditions have been established in the uppermost aquifer (Tertiary gravels) at the Gunnison disposal site. The monitor well locations provide a representative distribution of sampling points to characterize ground water quality and ground water flow conditions in the vicinity of the sites. The list of analytes has been modified with time to reflect constituents that are related to uranium processing activities and the parameters needed for geochemical evaluation. Water sampling will be conducted at least semiannually during and one year following the period of construction activities, to comply with the ground water protection strategy discussed in the remedial action plan (DOE, 1992a)

Assessment of geochemical and hydrologic conditions near Old Yuma Mine in Saguaro National Park, Arizona, 2014–17

Science.gov (United States)

Beisner, Kimberly R.; Gray, Floyd

2018-03-13

The Old Yuma Mine is an abandoned copper, lead, zinc, silver, and gold mine located within the boundaries of Saguaro National Park, Tucson Mountain District, Arizona. This study analyzed the geochemistry of sediments associated with the Old Yuma Mine and assessed hydrologic and geochemical conditions of groundwater to evaluate the area surrounding the Old Yuma Mine. The purpose of the study was to establish the geochemical signature of material associated with the Old Yuma Mine and to compare it with background material and groundwater in the area. Few groundwater samples exceeded the U.S. Environmental Protection Agency (EPA) drinking water standards. Concentrations of several elements were elevated in the waste rock and mine tailings compared with concentrations in sediments collected in background areas. A subset of 15 sediment samples was leached to simulate precipitation interacting with the solid material. Analysis of leachate samples compared to groundwater samples suggests that groundwater samples collected in this study are distinct from leachate samples associated with mining related material. Results suggest that at this time groundwater samples collected during this investigation are not influenced by elements leached from Old Yuma Mine materials.

Geochemical investigation of UMTRAP designated site at Grand Junction, Colorado

International Nuclear Information System (INIS)

Markos, G.; Bush, K.J.

1983-09-01

This report is the result of a geochemical investigation of the former uranium mill and tailings site at Grand Junction, Colorado. The objectives of the investigation are to characterize the geochemistry, to determine the contaminant distribution resulting from the former milling activities and tailings, and to infer chemical pathways and transport mechanisms from the contaminant distribution. The results should be used to model contaminant migration and to develop criteria for long-term containment media, such as a cover system which is impermeable to contaminant migration. This report assumes a familiarity with the hydrologic conditions of the site and the geochemical concepts underlying the investigation. The results reported are based on a sampling of waters in two seasons and solid material from the background, the area adjacent to the site, and the site. The solid samples were water extracted to remove easily soluble salts and acid extracted to remove carbonates and hydroxides. The water extracts and solid samples were analyzed for the major and trace elements. A limited number of samples were analyzed for radiological components. The report includes the methods of sampling, sample processing, analysis, and data interpretation. Four major conclusions are: (1) trace element concentrations in shallow subsurface waters adjacent to the tailings temporally vary up to an order of magnitude; (2) the riverbank soils and borehole waters are contaminated with uranium, radium, and trace elements from discharge of tailings solids and solutions during the active time of the mill; however, the movement of contaminants toward the Colorado River does not appear to be significant; (3) the Colorado River adjacent to the tailings is not contaminated; and (4) trace metals have accumulated at both the tailings/cover and tailings/soil interface because of precipitation reactions caused by chemical differences between the two materials

Development of digital gamma-activation autoradiography for analysis of samples of large area

International Nuclear Information System (INIS)

Kolotov, V.P.; Grozdov, D.S.; Dogadkin, N.N.; Korobkov, V.I.

2011-01-01

Gamma-activation autoradiography is a prospective method for screening detection of inclusions of precious metals in geochemical samples. Its characteristics allow analysis of thin sections of large size (tens of cm2), that favourably distinguishes it among the other methods for local analysis. At the same time, the activating field of the accelerator bremsstrahlung, displays a sharp intensity decrease relative to the distance along the axis. A method for activation dose ''equalization'' during irradiation of the large size thin sections has been developed. The method is based on the usage of a hardware-software system. This includes a device for moving the sample during the irradiation, a program for computer modelling of the acquired activating dose for the chosen kinematics of the sample movement and a program for pixel-by pixel correction of the autoradiographic images. For detection of inclusions of precious metals, a method for analysis of the acquired dose dynamics during sample decay has been developed. The method is based on the software processing pixel by pixel a time-series of coaxial autoradiographic images and generation of the secondary meta-images allowing interpretation regarding the presence of interesting inclusions based on half-lives. The method is tested for analysis of copper-nickel polymetallic ores. The developed solutions considerably expand the possible applications of digital gamma-activation autoradiography. (orig.)

Development of digital gamma-activation autoradiography for analysis of samples of large area

Energy Technology Data Exchange (ETDEWEB)

Kolotov, V.P.; Grozdov, D.S.; Dogadkin, N.N.; Korobkov, V.I. [Russian Academy of Sciences, Moscow (Russian Federation). Vernadsky Inst. of Geochemistry and Analytical Chemistry

2011-07-01

Gamma-activation autoradiography is a prospective method for screening detection of inclusions of precious metals in geochemical samples. Its characteristics allow analysis of thin sections of large size (tens of cm2), that favourably distinguishes it among the other methods for local analysis. At the same time, the activating field of the accelerator bremsstrahlung, displays a sharp intensity decrease relative to the distance along the axis. A method for activation dose ''equalization'' during irradiation of the large size thin sections has been developed. The method is based on the usage of a hardware-software system. This includes a device for moving the sample during the irradiation, a program for computer modelling of the acquired activating dose for the chosen kinematics of the sample movement and a program for pixel-by pixel correction of the autoradiographic images. For detection of inclusions of precious metals, a method for analysis of the acquired dose dynamics during sample decay has been developed. The method is based on the software processing pixel by pixel a time-series of coaxial autoradiographic images and generation of the secondary meta-images allowing interpretation regarding the presence of interesting inclusions based on half-lives. The method is tested for analysis of copper-nickel polymetallic ores. The developed solutions considerably expand the possible applications of digital gamma-activation autoradiography. (orig.)

Uruguay Mining inventory. Minas fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H.; Artignan, D.; Vairon, P.

1982-01-01

This work is about the geochemical prospecting carried out in Minas fotoplano within the framework of Uruguay Mining inventory. In this work were covered 380 km2 obtaining with 433 samples for study which were analized by Plasma Emission Spectrometry in Orleans BRGM laboratories

Panay carborne radiometric and geochemical surveys

International Nuclear Information System (INIS)

Santos, G. Jr.

1981-09-01

A carborne radiometric survey and stream sediments collection were conducted in Panay and Guimaras Islands. An area in Nabas, Aklan, situated in the northwestern tip of Panay (Buruanga Peninsula) which indicated 2 to 3 times above background radioactivity was delineated. Uranium content in the stream sediment samples collected from Buruanga Peninsula was generally higher than those obtained in other parts of the island. Radioactivity measurements and uranium content in stream sediments were found to be within background levels. It is recommended that follow-up radiometric and geochemical surveys be undertaken in Buruanga Peninsula and additional stream sediments samples be collected in Panay to achieve better sampling density and coverage. (author)

Geochemical signature of radioactive waste: oil NORM

International Nuclear Information System (INIS)

Costa, Gilberto T. de Paula; Costa-de-Moura, Jorge; Gomes, Carlos de Almeida; Sampaio, Emidio A. Lopes

2017-01-01

The Brazilian Nuclear Agency (CNEN) rules all nuclear activity in Brazil as demanded by the Federal Constitution, articles 21, XXIII, and 177, V, and by the Federal Acts 4.118/62 and 10.308/2001. Therefore, the CNEN is responsible for any radioactive waste disposal in the country. Oil Naturally Occurring Radioactive Materials (Oil NORM) in this paper refers to waste coming from oil exploration. Oil NORM has called much attention during the last decades, mostly because it is not possible to determine its primary source due to the actual absence of regulatory control mechanism. There is no efficient regulatory tool which allows determining the origin of such NORM wastes even among those facilities under regulatory control. This fact may encourage non-authorized radioactive material transportation, smuggling and terrorism. The aim of this project is to provide a geochemical signature for each oil NORM waste using its naturally occurring isotopic composition to identify its origin. The here proposed method is a specific geochemical modeling of oil sludge NORM samples which are analyzed for radioisotopes normally present in oil pipes, such as 228 Ac, 214 Bi and 214 Pb. The activity ratios are plotted in scatter diagrams. This method was successfully tested with data of different sources obtained from analysis reports from the Campos Basin/Brazil and from literature. (author)

Geochemical signature of radioactive waste: oil NORM

Energy Technology Data Exchange (ETDEWEB)

Costa, Gilberto T. de Paula; Costa-de-Moura, Jorge; Gomes, Carlos de Almeida; Sampaio, Emidio A. Lopes, E-mail: gilberto.costa@cnen.gov.br, E-mail: jcmoura@cnen.gov.br, E-mail: cgomes@cnen.gov.br [Comissao Nacional de Energia Nuclear (CNEN), Rio de Janeiro, RJ (Brazil). Div. de Controle de Rejeitos e Transporte de Materiais Radioativos

2017-07-01

The Brazilian Nuclear Agency (CNEN) rules all nuclear activity in Brazil as demanded by the Federal Constitution, articles 21, XXIII, and 177, V, and by the Federal Acts 4.118/62 and 10.308/2001. Therefore, the CNEN is responsible for any radioactive waste disposal in the country. Oil Naturally Occurring Radioactive Materials (Oil NORM) in this paper refers to waste coming from oil exploration. Oil NORM has called much attention during the last decades, mostly because it is not possible to determine its primary source due to the actual absence of regulatory control mechanism. There is no efficient regulatory tool which allows determining the origin of such NORM wastes even among those facilities under regulatory control. This fact may encourage non-authorized radioactive material transportation, smuggling and terrorism. The aim of this project is to provide a geochemical signature for each oil NORM waste using its naturally occurring isotopic composition to identify its origin. The here proposed method is a specific geochemical modeling of oil sludge NORM samples which are analyzed for radioisotopes normally present in oil pipes, such as {sup 228}Ac, {sup 214}Bi and {sup 214}Pb. The activity ratios are plotted in scatter diagrams. This method was successfully tested with data of different sources obtained from analysis reports from the Campos Basin/Brazil and from literature. (author)

Geochemical characterization of fluoride in water, table salt, active sediment, rock and soil samples, and its possible relationship with the prevalence of enamel fluorosis in children in four municipalities of the department of Huila (Colombia).

Science.gov (United States)

Martignon, Stefania; Opazo-Gutiérrez, Mario Omar; Velásquez-Riaño, Möritz; Orjuela-Osorio, Iván Rodrigo; Avila, Viviana; Martinez-Mier, Esperanza Angeles; González-Carrera, María Clara; Ruiz-Carrizosa, Jaime Alberto; Silva-Hermida, Blanca Cecilia

2017-06-01

Fluoride is an element that affects teeth and bone formation in animals and humans. Though the use of systemic fluoride is an evidence-based caries preventive measure, excessive ingestion can impair tooth development, mainly the mineralization of tooth enamel, leading to a condition known as enamel fluorosis. In this study, we investigated the geochemical characterization of fluoride in water, table salt, active sediment, rock and soil samples in four endemic enamel fluorosis sentinel municipalities of the department of Huila, Colombia (Pitalito, Altamira, El Agrado and Rivera), and its possible relationship with the prevalence of enamel fluorosis in children. The concentration of fluoride in drinking water, table salt, active sediment, rock, and soil was evaluated by means of an ion selective electrode and the geochemical analyses were performed using X-ray fluorescence. Geochemical analysis revealed fluoride concentrations under 15 mg/kg in active sediment, rock and soil samples, not indicative of a significant delivery to the watersheds studied. The concentration of fluoride in table salt was found to be under the inferior limit (less than 180 μg/g) established by the Colombian regulations. Likewise, exposure doses for fluoride water intake did not exceed the recommended total dose for all ages from 6 months. Although the evidence does not point out at rocks, soils, fluoride-bearing minerals, fluoridated salt and water, the hypothesis of these elements as responsible of the current prevalence of enamel fluorosis cannot be discarded since, aqueducts might have undergone significant changes overtime.

Geochemical prospecting for thorium and uranium deposits

International Nuclear Information System (INIS)

Boyle, R.W.

1982-01-01

The basic purpose of this book is to present an analysis of the various geochemical methods applicable in the search for all types of thorium and uranium deposits. The general chemistry and geochemistry of thorium and uranium are briefly described in the opening chapter, and this is followed by a chapter on the deposits of the two elements with emphasis on their indicator (pathfinder) elements and on the primary and secondary dispersion characteristics of thorium and uranium in the vicinity of their deposits. The next seven chapters form the main part of the book and describe geochemical prospecting for thorium and uranium, stressing selection of areas in which to prospect, radiometric surveys, analytical geochemical surveys based on rocks (lithochemical surveys), unconsolidated materials (pedochemical surveys), natural waters and sediments (hydrochemical surveys), biological materials (biogeochemical surveys), gases (atmochemical surveys), and miscellaneous methods. A final brief chapter reviews radiometric and analytical methods for the detection and estimation of thorium and uranium. (Auth.)

TAPIR--Finnish national geochemical baseline database.

Science.gov (United States)

Jarva, Jaana; Tarvainen, Timo; Reinikainen, Jussi; Eklund, Mikael

2010-09-15

In Finland, a Government Decree on the Assessment of Soil Contamination and Remediation Needs has generated a need for reliable and readily accessible data on geochemical baseline concentrations in Finnish soils. According to the Decree, baseline concentrations, referring both to the natural geological background concentrations and the diffuse anthropogenic input of substances, shall be taken into account in the soil contamination assessment process. This baseline information is provided in a national geochemical baseline database, TAPIR, that is publicly available via the Internet. Geochemical provinces with elevated baseline concentrations were delineated to provide regional geochemical baseline values. The nationwide geochemical datasets were used to divide Finland into geochemical provinces. Several metals (Co, Cr, Cu, Ni, V, and Zn) showed anomalous concentrations in seven regions that were defined as metal provinces. Arsenic did not follow a similar distribution to any other elements, and four arsenic provinces were separately determined. Nationwide geochemical datasets were not available for some other important elements such as Cd and Pb. Although these elements are included in the TAPIR system, their distribution does not necessarily follow the ones pre-defined for metal and arsenic provinces. Regional geochemical baseline values, presented as upper limit of geochemical variation within the region, can be used as trigger values to assess potential soil contamination. Baseline values have also been used to determine upper and lower guideline values that must be taken into account as a tool in basic risk assessment. If regional geochemical baseline values are available, the national guideline values prescribed in the Decree based on ecological risks can be modified accordingly. The national geochemical baseline database provides scientifically sound, easily accessible and generally accepted information on the baseline values, and it can be used in various

Reconnaissance geochemical survey for uranium and related industrial minerals in Cebu Island

International Nuclear Information System (INIS)

Reyes, R.Y.; Ramos, A.F.; Magsambol, W.N.; Hernandez, E.

1989-03-01

Consistent with the program of evaluating the nuclear mineral resource potential and related industrial minerals of the Philippines, a reconnaissance geochemical survey was conducted in Cebu with considerable success. The total area covered by the survey was about 5,088 sq. kms. The survey consisted of systematic collection of 857 geochemical stream and water and heavy mineral samples, and measurement of radioactivity in over 352 stations. The average sampling density was about one set of samples per 15 to 30 sq. kms. All solid samples were analyzed for U, Cu, Pb, Zn, Mn, Ag, Co and Ni. Uranium, radon and conductivity were measured on most water samples collected. A total of 4,518 elemental determinations were involved. All field and analytical data were treated by statistics, and the computed parameters data were correlated with the geology of the area to establish anomalous zones. Four areas were delineated for possible uranium mineralization. Of the areas, the Mandaue river area is the most interesting for uranium. The contact zone between the diorite and the sedimentary rocks in this area appears to be a favorable geological environment for uranium mineralization. The other anomalous uranium values were found to be related with the guano and phosphate deposits. Uranium was also shown to be independent of the other seven elements in the geologic environment of Cebu. No definite elemental association could be established at present. This study also marks the thorough utilization of Q'GAS, Cadplot and Autocad, all microcomputer-based programs/systems, in the evaluation and interpretation of exploration-oriented geochemical and geological data, and with more significance in the sense that computer generated quality geochemical maps were produced, a first in the country. (Author). Appendices (23); 23 figs; 13 refs.; 4 tabs

Neutron activation analysis of rare earths and some other elements in material of geochemical interest

International Nuclear Information System (INIS)

Brunfelt, A.O.

1975-01-01

ngle-element methods for the determination by neutron activation analysis of antimony, chromium, phosphorus, selenium and silver in international geochemical standard rocks, and the determination of rare earth elements i in standard rocks and apatites are described and discussed in twelve previously published papers, and in an eighteen page summary. Chemical separationtechniques are also discussed and the results are compared with previously obtained results with the same standard rocks. The accuracy of neutron activation analysis is discussed in comparison with isotope dilution mass spectroscopy, atomic absorption, gas chromatography and spark source mass spectrometry. (JIW)

Analysis of eight argonne premium coal samples by X-ray fluorescence spectrometry

Science.gov (United States)

Evans, J.R.; Sellers, G.A.; Johnson, R.G.; Vivit, D.V.; Kent, J.

1990-01-01

X-ray fluorescence spectrometric methods were used in the analysis of eight Argonne Premium Coal Samples. Trace elements (Cr, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, La, and Ce) in coal ash were determined by energy-dispersive X-ray fluorescence spectrometry; major elements (Na, Mg, Al, Si, P, S, K, Ca, Ti, Mn, and Fe) in coal ash and trace elements (Cl and P) in whole coal were determined by wavelength-dispersive X-ray fluorescence spectrometry. The results of this study will be used in a geochemical database compiled for these materials from various analytical techniques. The experimental XRF methods and procedures used to determine these major and trace elements are described.

Geochemical Investigations of Groundwater Stability

Energy Technology Data Exchange (ETDEWEB)

Bath, Adrian [Intellisci Ltd., Loughborough (United Kingdom)

2006-05-15

local palaeohydrogeological conditions. It is likely that inland areas have had longer durations of post-glacial fresh water infiltration than coastal areas, possibly causing greater degrees of dilution and dispersion of preexisting groundwaters and thus overprinting their hydrochemical and isotopic 'fingerprints'. Lower post-glacial hydraulic gradients relative to inland sites may account for the occurrence of more relict cold-climate water at coastal sites. Some general observations are based on rather thin evidence and therefore speculative. Firstly, it seems that glacial melt water penetrated many hundreds of metres and in some places to at least 1,000 m depth. However the low remaining proportions of melt water and of much older saline Shield water suggest that melt water flux did not fully displace pre-existing groundwaters at these depths. Secondly, where there has been post-glacial infiltration of palaeo-Baltic sea water, the density stratification or compartmentalisation effect coupled with low hydraulic gradient has reduced rates of subsequent fresh water circulation after shoreline recession. There are many uncertainties in interpreting these geochemical indicators in terms of the penetration depths of glacial melt waters and the degree to which they replace preexisting groundwaters, of other aspects of groundwater stability, and of comparisons between inland and coastal groundwater systems. Uncertainties derive partly from the reliability of groundwater samples as being representative of in situ conditions, and partly from the non-uniqueness of interpretative models. Future investigations using these approaches need to improve sampling, to make conjunctive use of geochemical and isotopic indicators which have varying timescales and sensitivities, and to integrate these indicators with palaeohydrogeological modelling to support the development of reliable groundwater flow and solute transport models for Performance Assessment.

Using geochemical indicators to distinguish high biogeochemical activity in floodplain soils and sediments

Energy Technology Data Exchange (ETDEWEB)

Kenwell, Amy [Hydrologic Sciences and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Navarre-Sitchler, Alexis, E-mail: asitchle@mines.edu [Hydrologic Sciences and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Prugue, Rodrigo [Hydrologic Sciences and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Spear, John R. [Department of Civil and Environmental Engineering, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Hering, Amanda S. [Department of Applied Mathematics and Statistics, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Maxwell, Reed M. [Hydrologic Sciences and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Carroll, Rosemary W.H. [Desert Research Institute, Division of Hydrologic Sciences, 2215 Raggio Parkway, Reno, NV 89512 (United States); Williams, Kenneth H. [Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States)

2016-09-01

A better understanding of how microbial communities interact with their surroundings in physically and chemically heterogeneous subsurface environments will lead to improved quantification of biogeochemical reactions and associated nutrient cycling. This study develops a methodology to predict potential elevated rates of biogeochemical activity (microbial “hotspots”) in subsurface environments by correlating microbial DNA and aspects of the community structure with the spatial distribution of geochemical indicators in subsurface sediments. Multiple linear regression models of simulated precipitation leachate, HCl and hydroxylamine extractable iron and manganese, total organic carbon (TOC), and microbial community structure were used to identify sample characteristics indicative of biogeochemical hotspots within fluvially-derived aquifer sediments and overlying soils. The method has been applied to (a) alluvial materials collected at a former uranium mill site near Rifle, Colorado and (b) relatively undisturbed floodplain deposits (soils and sediments) collected along the East River near Crested Butte, Colorado. At Rifle, 16 alluvial samples were taken from 8 sediment cores, and at the East River, 46 soil/sediment samples were collected across and perpendicular to 3 active meanders and an oxbow meander. Regression models using TOC and TOC combined with extractable iron and manganese results were determined to be the best fitting statistical models of microbial DNA (via 16S rRNA gene analysis). Fitting these models to observations in both contaminated and natural floodplain deposits, and their associated alluvial aquifers, demonstrates the broad applicability of the geochemical indicator based approach. - Highlights: • Biogeochemical characterization of alluvial floodplain soils and sediments was performed to investigate parameters that may indicate microbial hot spot formation. • A correlation between geochemical parameters (total organic carbon and

Using geochemical indicators to distinguish high biogeochemical activity in floodplain soils and sediments

International Nuclear Information System (INIS)

Kenwell, Amy; Navarre-Sitchler, Alexis; Prugue, Rodrigo; Spear, John R.; Hering, Amanda S.; Maxwell, Reed M.; Carroll, Rosemary W.H.; Williams, Kenneth H.

2016-01-01

A better understanding of how microbial communities interact with their surroundings in physically and chemically heterogeneous subsurface environments will lead to improved quantification of biogeochemical reactions and associated nutrient cycling. This study develops a methodology to predict potential elevated rates of biogeochemical activity (microbial “hotspots”) in subsurface environments by correlating microbial DNA and aspects of the community structure with the spatial distribution of geochemical indicators in subsurface sediments. Multiple linear regression models of simulated precipitation leachate, HCl and hydroxylamine extractable iron and manganese, total organic carbon (TOC), and microbial community structure were used to identify sample characteristics indicative of biogeochemical hotspots within fluvially-derived aquifer sediments and overlying soils. The method has been applied to (a) alluvial materials collected at a former uranium mill site near Rifle, Colorado and (b) relatively undisturbed floodplain deposits (soils and sediments) collected along the East River near Crested Butte, Colorado. At Rifle, 16 alluvial samples were taken from 8 sediment cores, and at the East River, 46 soil/sediment samples were collected across and perpendicular to 3 active meanders and an oxbow meander. Regression models using TOC and TOC combined with extractable iron and manganese results were determined to be the best fitting statistical models of microbial DNA (via 16S rRNA gene analysis). Fitting these models to observations in both contaminated and natural floodplain deposits, and their associated alluvial aquifers, demonstrates the broad applicability of the geochemical indicator based approach. - Highlights: • Biogeochemical characterization of alluvial floodplain soils and sediments was performed to investigate parameters that may indicate microbial hot spot formation. • A correlation between geochemical parameters (total organic carbon and

Geochemical indicators of gold ore fields

International Nuclear Information System (INIS)

Shcherbakov, Yu.G.

1995-01-01

The principles of selection of indicators for genetic reconstructions and prognostic valuations of gold mineralization of diverse morphological and geochemical types have been substantiated. The neutron-activation analysis with radiochemical separation and detection limit of 1-10 -8 %, instrumental neutron-activation analysis and atomic-absorption analysis are the main methods of determination of gold low contents in the rocks, as well as diverse elements, including transition, rare earth elements and tellurium, in gold. 50 refs.; 1 fig.; 3 tabs

Mining inventory of Uruguay. Polanco fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H; Artignan, D; Vairon, P

1982-01-01

This work is about the geochemical prospecting carried out in Polanco fotoplano within the framework of Uruguay Mining inventory . In this work were covered 660 km2 obtaining 685 samples for study which were analyzed by Plasma Emission Spectrometry in Orleans BRGM laboratories

Geochemical landscapes of the conterminous United States; new map presentations for 22 elements

Science.gov (United States)

Gustavsson, N.; Bolviken, B.; Smith, D.B.; Severson, R.C.

2001-01-01

Geochemical maps of the conterminous United States have been prepared for seven major elements (Al, Ca, Fe, K, Mg, Na, and Ti) and 15 trace elements (As, Ba, Cr, Cu, Hg, Li, Mn, Ni, Pb, Se, Sr, V, Y, Zn, and Zr). The maps are based on an ultra low-density geochemical survey consisting of 1,323 samples of soils and other surficial materials collected from approximately 1960-1975. The data were published by Boerngen and Shacklette (1981) and black-and-white point-symbol geochemical maps were published by Shacklette and Boerngen (1984). The data have been reprocessed using weighted-median and Bootstrap procedures for interpolation and smoothing.

Geochemical Data for Samples Collected in 2007 Near the Concealed Pebble Porphyry Cu-Au-Mo Deposit, Southwest Alaska

Science.gov (United States)

Fey, David L.; Granitto, Matthew; Giles, Stuart A.; Smith, Steven M.; Eppinger, Robert G.; Kelley, Karen D.

2008-01-01

In the summer of 2007, the U.S. Geological Survey (USGS) began an exploration geochemical research study over the Pebble porphyry copper-gold-molydenum (Cu-Au-Mo) deposit in southwest Alaska. The Pebble deposit is extremely large and is almost entirely concealed by tundra, glacial deposits, and post-Cretaceous volcanic and volcaniclastic rocks. The deposit is presently being explored by Northern Dynasty Minerals, Ltd., and Anglo-American LLC. The USGS undertakes unbiased, broad-scale mineral resource assessments of government lands to provide Congress and citizens with information on national mineral endowment. Research on known deposits is also done to refine and better constrain methods and deposit models for the mineral resource assessments. The Pebble deposit was chosen for this study because it is concealed by surficial cover rocks, it is relatively undisturbed (except for exploration company drill holes), it is a large mineral system, and it is fairly well constrained at depth by the drill hole geology and geochemistry. The goals of the USGS study are (1) to determine whether the concealed deposit can be detected with surface samples, (2) to better understand the processes of metal migration from the deposit to the surface, and (3) to test and develop methods for assessing mineral resources in similar concealed terrains. This report presents analytical results for geochemical samples collected in 2007 from the Pebble deposit and surrounding environs. The analytical data are presented digitally both as an integrated Microsoft 2003 Access? database and as Microsoft 2003 Excel? files. The Pebble deposit is located in southwestern Alaska on state lands about 30 km (18 mi) northwest of the village of Illiamna and 320 km (200 mi) southwest of Anchorage (fig. 1). Elevations in the Pebble area range from 287 m (940 ft) at Frying Pan Lake just south of the deposit to 1146 m (3760 ft) on Kaskanak Mountain about 5 km (5 mi) to the west. The deposit is in an area of

Multi-Element Analysis and Geochemical Spatial Trends of Groundwater in Rural Northern New York

Directory of Open Access Journals (Sweden)

Michael O’Connor

2010-05-01

Full Text Available Samples from private wells (n = 169 throughout St. Lawrence County, NY were analyzed by ICP-MS multi-element techniques. St. Lawrence County spans three diverse bedrock terranes including Precambrian crystalline rocks of the Adirondack Lowlands (mostly paragneisses and Highlands (mostly orthogneisses, as well as Paleozoic sedimentary rocks of the St. Lawrence Valley. An ArcGIS database was constructed and used to generate contour plots for elements across the county. Strontium isotopes and unique geochemical signatures were used to distinguish water from various geologic units. The results were consistent with a large (7,309 km2, sparsely populated (~110,000, rural region with diverse bedrock and glacial cover.

DEPOSITIONAL ENVIRONMENT AND ORGANIC GEOCHEMICAL CHARACTERISTICS OF LOWER EOCENE BITUMINOUS ROCKS, IN THE KÜRNÜÇ/GÖYNÜK-BOLU AREA

Directory of Open Access Journals (Sweden)

Ali SARI

2016-12-01

Full Text Available In this study, dark gray and dark brown colored, organic-carbon rich bituminous rocks (bituminous marl and bituminous shale exposing around the Kürnüç area (Göynük, Bolu are investigated by means of or- ganic geochemical characteristics. In this respect, rock lithologies, depositional environments, rock source potential, kerogen and organic maturity types and hydrocarbon generation potentials of bituminous rocks were determined. For this reason, pyrolysis (Rock Eval–VI analysis, gas chromatography (GC and gas chromatography-mass spectrometer (GC-MS analyses were carried out. In addition, spore color index (SCI was determined with organic petrographic method and stable carbon analysis (δ13C of the samples were also conducted. Lithology of the studied samples is of clastic source and the depositional environ- ment is a lagoon with a partial connection to the sea. In bituminous rocks with excellent source rock potential TOC values are in the range of 2.52-8.38 wt % (average 6.08 wt %. With the exception of two samples (Type II kerogen type of all samples is Type I. According to pyrolysis, GC and GC-MS organic maturity results, all the samples are in immature stage. Organic geochemical data indicate that bituminous rocks have an excellent oil generation potential and there is no organic contamination.

Uruguay Mining inventory. Las Animas fotoplano geochemical prospecting results

International Nuclear Information System (INIS)

Zeegers, H.; Spangenberg, J.

1981-01-01

This work is about the geochemical prospecting carried out in Las Animas fotoplano within the framework of Uruguay Mining inventory. In this work were covered 660 km2 obtaining 738 samples for study which were analyzed by Plasma Emission Spectrometry in Orleans BRGM laboratories.

Coupled geochemical and solute transport code development

International Nuclear Information System (INIS)

Morrey, J.R.; Hostetler, C.J.

1985-01-01

A number of coupled geochemical hydrologic codes have been reported in the literature. Some of these codes have directly coupled the source-sink term to the solute transport equation. The current consensus seems to be that directly coupling hydrologic transport and chemical models through a series of interdependent differential equations is not feasible for multicomponent problems with complex geochemical processes (e.g., precipitation/dissolution reactions). A two-step process appears to be the required method of coupling codes for problems where a large suite of chemical reactions must be monitored. Two-step structure requires that the source-sink term in the transport equation is supplied by a geochemical code rather than by an analytical expression. We have developed a one-dimensional two-step coupled model designed to calculate relatively complex geochemical equilibria (CTM1D). Our geochemical module implements a Newton-Raphson algorithm to solve heterogeneous geochemical equilibria, involving up to 40 chemical components and 400 aqueous species. The geochemical module was designed to be efficient and compact. A revised version of the MINTEQ Code is used as a parent geochemical code

Predictive Analysis of Geochemical Controls in an Alpine Stream

Science.gov (United States)

Jochems, A. P.; Sherson, L. R.; Crossey, L. J.; Karlstrom, K. E.

2010-12-01

Alpine watersheds are increasingly relied upon for use in the American West, necessitating a more complete understanding of annual hydrologic patterns and geologic influences on water chemistry. The Jemez River is a fifth order stream in central New Mexico that flows from its source in the Jemez Mountains to its confluence with the Rio Grande north of the town of Bernalillo. Designated uses of the Jemez River include domestic water supply, recreation, and agriculture. Geothermal uses are currently being considered as well. The river recharges shallow aquifer waters used by several communities, including tribal lands of the Jemez Pueblo. The hydrogeology of the Jemez system is characterized by geothermal inputs from the Baca hydrothermal system associated with the 1.2Ma Valles caldera, as well as groundwater and surface water interactions. Freshwater input from the Rio Guadalupe and several ephemeral tributaries also influences the water chemistry of the Jemez system. Fifteen sites along a 35 km reach of the river were sampled between 2006 and 2010. Discharge of the Jemez River ranged from 10-876 cfs over the study period. The annual hydrograph is affected by annual snowmelt in the Jemez Mountains as well as surges due to monsoonal rains in July and August. Geochemical data collected over this period include temperature, conductivity, pH, dissolved oxygen (D.O.), major ions, trace elements, and stable isotopes. Continuous records of temperature, conductivity, pH, D.O. and turbidity data were collected from a water quality sonde installed in March 2010. Geochemical modeling and time series analysis were performed using PHREEQC, Geochemist’s Workbench, and MATLAB. Empirical data collected during this study gave rise to several models describing the hydrology and geochemistry of the Jemez system. Our data suggest that springs are the primary contributors to dissolved load, and that solute loading from geothermal inputs is intensified by low flows observed on

A comparison of geochemical exploration techniques and sample media within accretionary continental margins: an example from the Pacific Border Ranges, Southern Alaska, U.S.A.

Science.gov (United States)

Sutley, S.J.; Goldfarb, R.J.; O'Leary, R. M.; Tripp, R.B.

1990-01-01

The Pacific Border Ranges of the southern Alaskan Cordillera are composed of a number of allochthonous tectonostratigraphic terranes. Within these terranes are widespread volcanogenic, massive sulfide deposits in and adjacent to portions of accreted ophiolite complexes, bands and disseminations of chromite in accreted island-arc ultramafic rocks, and epigenetic, gold-bearing quartz veins in metamorphosed turbidite sequences. A geochemical pilot study was undertaken to determine the most efficient exploration strategy for locating these types of mineral deposits within the Pacific Border Ranges and other typical convergent continental margin environments. High-density sediment sampling was carried out in first- and second-order stream channels surrounding typical gold, chromite and massive sulfide occurrences. At each site, a stream-sediment and a panned-concentrate sample were collected. In the laboratory, the stream sediments were sieved into coarse-sand, fine- to medium-sand, and silt- to clay-size fractions prior to analysis. One split of the panned concentrates was retained for analysis; a second split was further concentrated by gravity separation in heavy liquids and then divided into magnetic, weakly magnetic and nonmagnetic fractions for analysis. A number of different techniques including atomic absorption spectrometry, inductively coupled plasma atomic emission spectrometry and semi-quantitative emission spectrography were used to analyze the various sample media. Comparison of the various types of sample media shows that in this tectonic environment it is most efficient to include a silt- to clay-size sediment fraction and a panned-concentrate sample. Even with the relatively low detection limits for many elements by plasma spectrometry and atomic absorption spectrometry, anomalies reflecting the presence of gold veins could not be identified in any of the stream-sediment fractions. Unseparated panned-concentrate samples should be analyzed by emission

The role of geochemical prospecting in phased uranium exploration. A case history

International Nuclear Information System (INIS)

Smith, A.Y.; Armour-Brown, A.; Olsen, H.; Lundberg, B.; Niesen, P.L.

1976-01-01

The commencement of a UNDP/IAEA uranium exploration project in Northern Greece in 1971 offered the opportunity to test and apply an exploration strategy based on a phased use of geochemical exploration methods. The paper reviews the exploration task, the strategy selected, and some results obtained. The project area (22000 km 2 ) was explored by car-borne survey, covering 15000 km of road and track. Concurrently, a stream sediment geochemical survey was begun which aimed at a nominal sample density of one sample per square kilometre. Samples were analysed for copper, lead, zinc, silver, cobalt, nickel, molybdenum, mercury and manganese, in addition to uranium. At each site, a general reading of radioactivity was made, and treated like another element analysis. The reconnaissance programme succeeded in delineating a number of important target areas, varying in size from a few to several hundred square kilometres with significant uranium potential. Follow-up and detailed surveys have been carried out over a number of these, including a sedimentary basin of continental deposits which have been found to contain occurrences of secondary uranium minerals, and two areas in which granitic bodies have been found to have fracture systems and secondary uranium mineralization of economic interest. In no case has sufficient work been yet done to prove economic deposits of uranium. The phased strategy used has, however, already been demonstrated to be effective in the environment of northern Greece. (author)

Determination of geochemical and natural radioactivity characteristics in Bilecik Marble, Turkey

Science.gov (United States)

Yerel Kandemir, Suheyla; Ozbay, Nurgul

2014-05-01

Natural stones are one of the oldest known building materials. There are more than 400 natural stone in Turkey. Recently, the demand for the natural stone types in markets has been increasing rapidly. For this reason, the geochemical and natural radioactivity characteristics of natural stone are very important. Bilecik province is located at the northwest part of Turkey and it is surrounded by Sakarya, Bursa, Eskisehir and Kutahya city. Bilecik is one of the important marble industry regions of Turkey. Thus, the geochemical and natural radioactivity characteristics of Bilecik marble are very important. In this study, Bilecik marble was collected to determine the geochemistry and natural radioactivity. Then, analyses of geochemical and natural radioactivity in the marble samples are interpreted. ACKNOWLEDGMENT This study is supported by Bilecik Seyh Edebali University scientific project (Project Number =2011-02-BIL.03-04).

Constraining Lateral Evolution of Magmatic Behavior in North Tanzania from Geophysical and Geochemical Analyses

Science.gov (United States)

Gautier, S.; Tiberi, C.; Parat, F.; Baudouin, C.

2016-12-01

In the framework of CRAFTI and CoLiBrEA experiments in 2013, we proceeded to both seismic and geochemical studies along an EW profile through the North Tanzania Divergence. The data were collected along a line starting at the Ngorongoro volcanic area, ending at Kitumbeine edifice and crossing the rift valley. Recent seismological studies show lateral and depth variations for both velocity and Vp/Vs ratio within this area, particularly a change of Moho depth between the western and central parts of the rift. These two zones also exhibit diverse geochemical signatures that involve different magma storage (depth of reservoir, magma volume) and ascent as well as higher partial melts content for the western part. We take advantage of the recent and precise 3D lithospheric velocity models and receiver functions in this area to compare the structure and nature of Ngorongoro area and rift valley. We first compute ray path and establish regional coherency maps between piercing points, Vp/Vs ratio and tomographic images. Second, those results are compared with the composition of magma at depth obtained from a petrophysical and geochemical analysis of lava samples. We will discuss those results in terms of magmatic processes, and how they interact with the rifting in a cratonic lithosphere.

Instrumenting caves to collect hydrologic and geochemical data: case study from James Cave, Virginia

Science.gov (United States)

Schreiber, Madeline E.; Schwartz, Benjamin F.; Orndorff, William; Doctor, Daniel H.; Eagle, Sarah D.; Gerst, Jonathan D.

2015-01-01

Karst aquifers are productive groundwater systems, supplying approximately 25 % of the world’s drinking water. Sustainable use of this critical water supply requires information about rates of recharge to karst aquifers. The overall goal of this project is to collect long-term, high-resolution hydrologic and geochemical datasets at James Cave, Virginia, to evaluate the quantity and quality of recharge to the karst system. To achieve this goal, the cave has been instrumented for continuous (10-min interval) measurement of the (1) temperature and rate of precipitation; (2) temperature, specific conductance, and rate of epikarst dripwater; (3) temperature of the cave air; and (4) temperature, conductivity, and discharge of the cave stream. Instrumentation has also been installed to collect both composite and grab samples of precipitation, soil water, the cave stream, and dripwater for geochemical analysis. This chapter provides detailed information about the instrumentation, data processing, and data management; shows examples of collected datasets; and discusses recommendations for other researchers interested in hydrologic and geochemical monitoring of cave systems. Results from the research, briefly described here and discussed in more detail in other publications, document a strong seasonality of the start of the recharge season, the extent of the recharge season, and the geochemistry of recharge.

Sampling and chemical analysis of groundwaters from the exploratory boreholes

International Nuclear Information System (INIS)

Wittwer, C.

1986-10-01

As a part of the Nagra geological investigation programme in northern Switzerland, numerous water samples were taken in the Boettstein, Weiach, Riniken, Schafisheim, Kaisten and Leuggern boreholes to obtain information on the chemistry and residence times of deep groundwaters. This report contains a compilation of hydrochemical data, comments on the individual water sampling actions and an evaluation of sample quality with respect to admixing of drilling fluids. The samples were taken from separate test intervals in the sediments and the crystalline rock. After removal of various types of drilling fluids such as mud as well as fresh water or deionised water during a cleaning phase, the samples were taken at the surface or at depth using pressure vessels. The tracers added to the drilling fluids (uranine, m-TFMBA) as well as the tritium content were used for a quantiative estimation of the content of drilling fluid in the samples (contamination). With a view fo further geochemical modelling, the samples were assessed with reference to the effect of contamination on the results of the chemical analyses. A total of 68 water samples were taken from 53 different intervals: - 27 samples had problem-free cleaning phases and were taken with negligible contamination. - 23 samples were taken under difficult conditions. Problems with hydraulic communication around packers, uncertain origin, inaccuracy as to extent of contamination, presence of cement, possible traces of salt from drilling fluid etc. meant that the analyses could only be used with extreme caution or after additional data-processing. - The analysis results from 18 samples will be disregarded due to significant drilling fluid content or because more reliable data are available for the same test interval. (author)

Geochemical Influence on Microbial Diversity in the Warm, Salty, Stinking Spring, Utah, USA

Science.gov (United States)

Spear, J. R.

2012-12-01

characterized at the two fast flowing sites. These two streamer varieties were dominated by either cyanobacteria or flavobacteria. Bicarbonate uptake in the light ranged from 0-2.1%/day with maximum rates found in floating, surface mats. Uptake in the dark ranged from 0-0.3%/day and was higher in lower layers. Both 16S rRNA analysis and pigment extractions showed no correlation between high autotrophic rates and presence of cyanobacteria or chlorophyll A. Lipid analysis showed no correlation between bicarbonate uptake and diatom abundance. The results suggest that carbon cycling in the various kinds of mats sampled is dominated by heterotrophs and anaerobic phototrophs despite abundant cyanobacteria and diatoms. A large depletion in sulfate from 16 mM to almost zero combined with low concentrations of measured sulfide and presence of elemental sulfur crystals in most mat samples indicate that the mats are a major sink of S in the system. Overall, our geochemical, genetic, lipid and bicarbonate analysis suggests that the physical and geochemical environment was more predictive of the community composition than mat morphology.

Collected radiochemical and geochemical procedures

Energy Technology Data Exchange (ETDEWEB)

Kleinberg, J [comp.

1990-05-01

This revision of LA-1721, 4th Ed., Collected Radiochemical Procedures, reflects the activities of two groups in the Isotope and Nuclear Chemistry Division of the Los Alamos National Laboratory: INC-11, Nuclear and radiochemistry; and INC-7, Isotope Geochemistry. The procedures fall into five categories: I. Separation of Radionuclides from Uranium, Fission-Product Solutions, and Nuclear Debris; II. Separation of Products from Irradiated Targets; III. Preparation of Samples for Mass Spectrometric Analysis; IV. Dissolution Procedures; and V. Geochemical Procedures. With one exception, the first category of procedures is ordered by the positions of the elements in the Periodic Table, with separate parts on the Representative Elements (the A groups); the d-Transition Elements (the B groups and the Transition Triads); and the Lanthanides (Rare Earths) and Actinides (the 4f- and 5f-Transition Elements). The members of Group IIIB-- scandium, yttrium, and lanthanum--are included with the lanthanides, elements they resemble closely in chemistry and with which they occur in nature. The procedures dealing with the isolation of products from irradiated targets are arranged by target element.

Geochemical and mineralogical analysis of stone anchors from west coast of India: Provenance study using thin sections, XRF and SEM-EDS

Digital Repository Service at National Institute of Oceanography (India)

Tripati, S.; Mudholkar, A.V.; Vora, K.H.; Rao, B.R.; Gaur, A.S.; Sundaresh

for petrographical and geochemical analysis. One surface of the rock chip was ground to finesmoothnessandwasmountedontotheglassslidewithhelp of Araldite C210 (resin & hardner) and then clamped to prevent developmentof air bubbles. After overnight cooling and curing...

Hydrogeological and geochemical monitoring system for deep disposal in rock mass

International Nuclear Information System (INIS)

Itoh, K.; Otsuka, Y.; Ohi, Y.

1996-01-01

For investigation and construction of deep underground disposal site, it is very important to monitor three dimensional hydrogeological and geochemical condition for long term in all stages of investigation, construction and management. In deep geological disposal site, permeability of rock mass should be extremely lower than conventional civil engineering field, and natural piezometric pressure should be much higher than conventional groundwater monitoring in civil engineering. So, pressure measuring device should have wide measuring range and high precision especially for interference hydraulic test in investigation stage. And, simultaneous pressure measurement in plural points would be required for cost minimization. Recently, some kinds of multi-point pressure monitoring system has been presented. However, most of all system requires borehole with large diameter, and for utilization in plural boreholes, centralized sensor control is very difficult. And, in groundwater sampling for geochemical investigation, it is important to keep original chemical condition through sampling and transportation from sampling depth to surface. For these purposes, the authors have developed multi well multi point piezometric pressure measuring device, and groundwater sampling system for 1,000m depth. (author)

Archean crust-mantle geochemical differentiation

Science.gov (United States)

Tilton, G. R.

Isotope measurements on carbonatite complexes and komatiites can provide information on the geochemical character and geochemical evolution of the mantle, including the sub-continental mantle. Measurements on young samples establish the validity of the method. These are based on Sr, Nd and Pb data from the Tertiary-Mesozoic Gorgona komatiite and Sr and Pb data from the Cretaceous Oka carbonatite complex. In both cases the data describe a LIL element-depleted source similar to that observed presently in MORB. Carbonatite data have been used to study the mantle beneath the Superior Province of the Canadian Shield one billion years (1 AE) ago. The framework for this investigation was established by Bell et al., who showed that large areas of the province appear to be underlain by LIL element-depleted mantle (Sr-85/Sr-86=0.7028) at 1 AE ago. Additionally Bell et al. found four complexes to have higher initial Sr ratios (Sr-87/Sr-86=0.7038), which they correlated with less depleted (bulk earth?) mantle sources, or possibly crustal contamination. Pb isotope relationships in four of the complexes have been studied by Bell et al.

Archean crust-mantle geochemical differentiation

Science.gov (United States)

Tilton, G. R.

1983-01-01

Isotope measurements on carbonatite complexes and komatiites can provide information on the geochemical character and geochemical evolution of the mantle, including the sub-continental mantle. Measurements on young samples establish the validity of the method. These are based on Sr, Nd and Pb data from the Tertiary-Mesozoic Gorgona komatiite and Sr and Pb data from the Cretaceous Oka carbonatite complex. In both cases the data describe a LIL element-depleted source similar to that observed presently in MORB. Carbonatite data have been used to study the mantle beneath the Superior Province of the Canadian Shield one billion years (1 AE) ago. The framework for this investigation was established by Bell et al., who showed that large areas of the province appear to be underlain by LIL element-depleted mantle (Sr-85/Sr-86=0.7028) at 1 AE ago. Additionally Bell et al. found four complexes to have higher initial Sr ratios (Sr-87/Sr-86=0.7038), which they correlated with less depleted (bulk earth?) mantle sources, or possibly crustal contamination. Pb isotope relationships in four of the complexes have been studied by Bell et al.

Petrologic and geochemical characterization of the Topopah Spring Member of the Paintbrush Tuff: outcrop samples used in waste package experiments

International Nuclear Information System (INIS)

Knauss, K.G.

1984-06-01

This report summarizes characterization studies conducted with outcrop samples of Topopah Spring Member of the Paintbrush Tuff (Tpt). In support of the Waste Package Task within the Nevada Nuclear Waste Storage Investigation (NNWSI), Tpt is being studied both as a primary object and as a constituent used to condition water that will be reacted with waste form, canister, or packing material. These studies directly or indirectly support NNWSI subtasks concerned with waste package design and geochemical modeling. To interpret the results of subtask experiments, it is necessary to know the exact nature of the starting material in terms of the intial bulk composition, mineralogy, and individual phase geochemistry. 31 figures, 5 tables

Petrologic and geochemical characterization of the Topopah Spring Member of the Paintbrush Tuff: outcrop samples used in waste package experiments

Energy Technology Data Exchange (ETDEWEB)

Knauss, K.G.

1984-06-01

This report summarizes characterization studies conducted with outcrop samples of Topopah Spring Member of the Paintbrush Tuff (Tpt). In support of the Waste Package Task within the Nevada Nuclear Waste Storage Investigation (NNWSI), Tpt is being studied both as a primary object and as a constituent used to condition water that will be reacted with waste form, canister, or packing material. These studies directly or indirectly support NNWSI subtasks concerned with waste package design and geochemical modeling. To interpret the results of subtask experiments, it is necessary to know the exact nature of the starting material in terms of the intial bulk composition, mineralogy, and individual phase geochemistry. 31 figures, 5 tables.

Geochemical Fractionations and Mobility of Arsenic, Lead and Cadmium in Sediments of the Kanto Plain, Japan.

Science.gov (United States)

Hossain, Sushmita; Oguchi, Chiaki T.; Hachinohe, Shoichi; Ishiyama, Takashi; Hamamoto, Hideki

2014-05-01

Lowland alluvial and floodplain sediment play a major role in transferring heavy metals and other elements to groundwater through sediment water interaction in changing environmental conditions. However identification of geochemical forms of toxic elements such as arsenic (As), lead (Pb) and cadmium (Cd) requires risk assessment of sediment and subsequent groundwater pollution. A four steps sequential extraction procedure was applied to characterize the geochemical fractionations of As, Pb and Cd for 44 sediment samples including one peat sample from middle basin area of the Nakagawa river in the central Kanto plain. The studied sediment profile extended from the bottom of the river to 44 m depth; sediment samples were collected at 1m intervals from a bored core. The existing sedimentary facies in vertical profile are continental, transitional and marine. There are two aquifers in vertical profile; the upper aquifer (15-20m) contains fine to medium sand whereas medium to coarse sand and gravelly sand contain in lower aquifer (37-44m). The total As and Pb contents were measured by the X-Ray Fluorescence analysis which ranged from 4 to 23 mg/kg of As and 10 to 27 mg/kg of Pb in sediment profile. The three trace elements and major heavy metals were determined by ICP/MS and ICP/AES, and major ions were measured by an ion chromatograph. The marine sediment is mainly Ca-SO4 type. The Geochemical analysis showed the order of mobility trends to be As > Pb > Cd for all the steps. The geochemical fractionations order was determined to be Fe-Mn oxide bound > carbonate bound > ion exchangeable > water soluble for As and Pb whereas the order for Cd is carbonate bound > Fe-Mn oxide bound > ion exchangeable > water soluble. The mobility tendency of Pb and Cd showed high in fine silty sediment of marine environment than for those from continental and transitional environments. In the case of As, the potential mobility is very high (>60%) in the riverbed sediments and clayey silt

Analysis of the potential geochemical reactions in the Enceladus' hydrothermal environment

Science.gov (United States)

Ramirez-Cabañas, A. K.; Flandes, A.

2017-12-01

Enceladus is the sixth largest moon of Saturn and differs from its other moons, because of its cryovolcanic geysers that emanate from its south pole. The instruments of the Cassini spacecraft reveal different compounds in the gases and the dust of the geysers, such as salts (sodium chloride, sodium bicarbonate and/or sodium carbonate), as well as silica traces (Postberg et al., 2008, 2009) that could be the result of a hydrothermal environment (Hsu et al., 2014, Sekine et al., 2014). By means of a thermodynamic analysis, we propose and evaluate potential geochemical reactions that could happen from the interaction between the nucleus surface and the inner ocean of Enceladus. These reactions may well lead to the origin of the compounds found in the geysers. From this analysis, we propose that, at least, two minerals must be present in the condritic nucleus of Enceladus: olivines (fayalite and fosterite) and feldspar (orthoclase and albite). Subsequently, taking as reference the hydrothermal processes that take place on Earth, we propose the different stages of a potential hydrothermal scenario for Enceladus.

Proceedings of the workshop on geochemical modeling

International Nuclear Information System (INIS)

1986-01-01

The following collection of papers was presented at a workshop on geochemical modeling that was sponsored by the Office of Civilian Radioactive Waste Management Program at the Lawrence Livermore National Laboratory (LLNL). The LLNL Waste Management Program sponsored this conference based on their belief that geochemical modeling is particularly important to the radioactive waste disposal project because of the need to predict the consequences of long-term water-rock interactions at the proposed repository site. The papers included in this volume represent a subset of the papers presented at the Fallen Leaf Lake Conference and cover a broad spectrum of detail and breadth in a subject that reflects the diverse research interests of the conference participants. These papers provide an insightful look into the current status of geochemical modeling and illustrate how various geochemical modeling codes have been applied to problems of geochemical interest. The emphasis of these papers includes traditional geochemical modeling studies of individual geochemical systems, the mathematical and theoretical development and refinement of new modeling capabilities, and enhancements of data bases on which the computations are based. The papers in this proceedings volume have been organized into the following four areas: Geochemical Model Development, Hydrothermal and Geothermal Systems, Sedimentary and Low Temperature Environments, and Data Base Development. The participants of this symposium and a complete list of the talks presented are listed in the appendices

Proceedings of the workshop on geochemical modeling

Energy Technology Data Exchange (ETDEWEB)

1986-01-01

The following collection of papers was presented at a workshop on geochemical modeling that was sponsored by the Office of Civilian Radioactive Waste Management Program at the Lawrence Livermore National Laboratory (LLNL). The LLNL Waste Management Program sponsored this conference based on their belief that geochemical modeling is particularly important to the radioactive waste disposal project because of the need to predict the consequences of long-term water-rock interactions at the proposed repository site. The papers included in this volume represent a subset of the papers presented at the Fallen Leaf Lake Conference and cover a broad spectrum of detail and breadth in a subject that reflects the diverse research interests of the conference participants. These papers provide an insightful look into the current status of geochemical modeling and illustrate how various geochemical modeling codes have been applied to problems of geochemical interest. The emphasis of these papers includes traditional geochemical modeling studies of individual geochemical systems, the mathematical and theoretical development and refinement of new modeling capabilities, and enhancements of data bases on which the computations are based. The papers in this proceedings volume have been organized into the following four areas: Geochemical Model Development, Hydrothermal and Geothermal Systems, Sedimentary and Low Temperature Environments, and Data Base Development. The participants of this symposium and a complete list of the talks presented are listed in the appendices.

Geochemical Investigation of the Arbuckle-Simpson Aquifer, South-Central Oklahoma, 2004-06

Science.gov (United States)

Christenson, Scott; Hunt, Andrew G.; Parkhurst, David L.

2009-01-01

A geochemical reconnaissance investigation of the Arbuckle-Simpson aquifer in south-central Oklahoma was initiated in 2004 to characterize the ground-water quality at an aquifer scale, to describe the chemical evolution of ground water as it flows from recharge areas to discharge in wells and springs, and to determine the residence time of ground water in the aquifer. Thirty-six water samples were collected from 32 wells and springs distributed across the aquifer for chemical analysis of major ions, trace elements, isotopes of oxygen and hydrogen, dissolved gases, and age-dating tracers. In general, the waters from wells and springs in the Arbuckle-Simpson aquifer are chemically suitable for all regulated uses, such as public supplies. Dissolved solids concentrations are low, with a median of 347 milligrams per liter (mg/L). Two domestic wells produced water with nitrate concentrations that exceeded the U.S. Environmental Protection Agency's nitrate maximum contaminant level (MCL) of 10 mg/L. Samples from two wells in the confined part of the aquifer exceeded the secondary maximum contaminant level (SMCL) for chloride of 250 mg/L and the SMCL of 500 mg/L for dissolved solids. Water samples from these two wells are not representative of water samples from the other wells and springs completed in the unconfined part of the aquifer. No other water samples from the Arbuckle-Simpson geochemical reconnaissance exceeded MCLs or SMCLs, although not every chemical constituent for which the U.S. Environmental Protection Agency has established a MCL or SMCL was analyzed as part of the Arbuckle-Simpson geochemical investigation. The major ion chemistry of 34 of the 36 samples indicates the water is a calcium bicarbonate or calcium magnesium bicarbonate water type. Calcium bicarbonate water type is found in the western part of the aquifer, which is predominantly limestone. Calcium magnesium bicarbonate water is found in the eastern part of the aquifer, which is predominantly a

LASL approach to uranium geochemical reconnaissance

Energy Technology Data Exchange (ETDEWEB)

Sharp, R.R. Jr.

1977-01-01

The US ERDA, as part of the NURE program, has initiated a nationwide Hydrogeochemical and Stream Sediment Reconnaissance (HSSR). The aims of the NURE program are to provide data on which to base more accurate estimates of US uranium reserves for long-range planning and to aid in meeting the nation's projected uranium demands into the next century. The HSSR objective is to complete, by 1980, a reconnaissance of the nation's surface waters, ground waters, and stream and lake sediments, to aid in assessment of uranium reserves and identification of areas of interest for exploration. Patterned after extensive uranium reconnaissance done in many other countries, the LASL project is comprised of the following five components: (1) organization and planning, which includes management, design, and execution; (2) field sampling, which includes orientation studies, generation of specifications, and contracting and inspection of field work; (3) sample receiving and analysis, which includes development of methods and hardware, quality assurance, and archival storage; (4) data handling and presentation, including verification, storage, output, and plotting; and (5) data evaluation and publication, which incorporates geochemical, geological, statistical, and empirical evaluation and report writing. The LASL approach to each component and the current status in each state are described.

LASL approach to uranium geochemical reconnaissance

International Nuclear Information System (INIS)

Sharp, R.R. Jr.

1977-01-01

The US ERDA, as part of the NURE program, has initiated a nationwide Hydrogeochemical and Stream Sediment Reconnaissance (HSSR). The aims of the NURE program are to provide data on which to base more accurate estimates of US uranium reserves for long-range planning and to aid in meeting the nation's projected uranium demands into the next century. The HSSR objective is to complete, by 1980, a reconnaissance of the nation's surface waters, ground waters, and stream and lake sediments, to aid in assessment of uranium reserves and identification of areas of interest for exploration. Patterned after extensive uranium reconnaissance done in many other countries, the LASL project is comprised of the following five components: (1) organization and planning, which includes management, design, and execution; (2) field sampling, which includes orientation studies, generation of specifications, and contracting and inspection of field work; (3) sample receiving and analysis, which includes development of methods and hardware, quality assurance, and archival storage; (4) data handling and presentation, including verification, storage, output, and plotting; and (5) data evaluation and publication, which incorporates geochemical, geological, statistical, and empirical evaluation and report writing. The LASL approach to each component and the current status in each state are described

Stand-off laser-induced breakdown spectroscopy of aluminum and geochemical reference materials at pressure below 1 torr

Energy Technology Data Exchange (ETDEWEB)

Lee, Kang-Jae; Choi, Soo-Jin; Yoh, Jack J., E-mail: jjyoh@snu.ac.kr

2014-11-01

Laser-induced breakdown spectroscopy (LIBS) is an atomic emission spectroscopy that utilizes a highly irradiated pulse laser focused on the target surface to produce plasma. We obtain spectroscopic information from the microplasma and determine the chemical composition of the sample based on its elemental and molecular emission peaks. We develop a stand-off LIBS system to analyze the effect of the remote sensing of aluminum and various geochemical reference materials at pressures below 1 torr. Using a commercial 4 inch refracting telescope, our stand-off LIBS system is configured at a distance of 7.2 m from the four United States Geological Survey (USGS) geochemical samples that include granodiorite, quartz latite, shale-cody, and diabase, which are selected for planetary exploration. Prepared samples were mixed with a paraffin binder containing only hydrogen and carbon, and were pelletized for experimental convenience. The aluminum plate sample is considered as a reference prior to using the geochemical samples in order to understand the influence of a low pressure condition on the resulting LIBS signal. A Q-switched Nd:YAG laser operating at 1064 nm and pulsed at 10 Hz with 21.7 to 48.5 mJ/pulse was used to obtain signals, which showed that the geochemical samples were successfully detected by the present stand-off detection scheme. A low pressure condition generally results in a decrease of the signal intensity, while the signal to noise ratio can vary according to the samples and elements of various types. We successfully identified the signals at below 1 torr with stand-off detection by a tightly focused light detection and by using a relatively larger aperture telescope. The stand-off LIBS detection at low pressure is promising for potential detection of the minor elements at pressures below 1 torr. - Highlights: • Stand-off LIBS signals at below 1 torr are compared to those of in-situ conditions. • Vacuum condition provides easier detection of the

Geochemical computer codes. A review

International Nuclear Information System (INIS)

Andersson, K.

1987-01-01

In this report a review of available codes is performed and some code intercomparisons are also discussed. The number of codes treating natural waters (groundwater, lake water, sea water) is large. Most geochemical computer codes treat equilibrium conditions, although some codes with kinetic capability are available. A geochemical equilibrium model consists of a computer code, solving a set of equations by some numerical method and a data base, consisting of thermodynamic data required for the calculations. There are some codes which treat coupled geochemical and transport modeling. Some of these codes solve the equilibrium and transport equations simultaneously while other solve the equations separately from each other. The coupled codes require a large computer capacity and have thus as yet limited use. Three code intercomparisons have been found in literature. It may be concluded that there are many codes available for geochemical calculations but most of them require a user that us quite familiar with the code. The user also has to know the geochemical system in order to judge the reliability of the results. A high quality data base is necessary to obtain a reliable result. The best results may be expected for the major species of natural waters. For more complicated problems, including trace elements, precipitation/dissolution, adsorption, etc., the results seem to be less reliable. (With 44 refs.) (author)

Geochemical characteristics of the Permian sedimentary rocks from Qiangtang Basin: Constraints for paleoenvironment and paleoclimate

Directory of Open Access Journals (Sweden)

Junjie Hu

2017-01-01

Full Text Available Qiangtang Basin is expected to become important strategic petroleum exploitation area in China. However, little research has been done on the Permian strata in this area. This paper presents Lower Permian Zhanjin Formation geochemical data from the Jiaomuri area, reconstructing the paleo-depositional environment and providing information for further petroleum exploration. The geochemical characteristics of 19 samples were investigated. These geochemical samples show a developed mud flat characteristic with light rich clay content. The geological data were used to constrain the paleoredox environment, which proved that these sediments were deposited mainly beneath a slightly oxic water column with relatively low paleoproductivity as evidenced by the P/Ti (mean of 0.07 and Ba/Al (mean of 20.5. Palaeoclimate indexes such as the C-value (0.24-1.75 and Sr/Cu (1.28-11.58 reveal a humid climatic condition during Zhanjin Formation sediment deposition. The ω(LaN/ω(YbN ratio values indicate a fast sedimentary rate during the deposition period.

UMTRA project water sampling and analysis plan, Naturita, Colorado

International Nuclear Information System (INIS)

1994-04-01

Surface remedial action is scheduled to begin at the Naturita UMTRA Project processing site in the spring of 1994. No water sampling was performed during 1993 at either the Naturita processing site (NAT-01) or the Dry Flats disposal site (NAT-12). Results of previous water sampling at the Naturita processing site indicate that ground water in the alluvium is contaminated as a result of uranium processing activities. Baseline ground water conditions have been established in the uppermost aquifer at the Dry Flats disposal site. Water sampling activities scheduled for April 1994 include preconstruction sampling of selected monitor wells at the processing site, surface water sampling of the San Miguel River, sampling of several springs/seeps in the vicinity of the disposal site, and sampling of two monitor wells in Coke Oven Valley. The monitor well locations provide sampling points to characterize ground water quality and flow conditions in the vicinity of the sites. The list of analytes has been updated to reflect constituents related to uranium processing activities and the parameters needed for geochemical evaluation. Water sampling will be conducted annually at minimum during the period of construction activities

Developing protocols for geochemical baseline studies: An example from the Coles Hill uranium deposit, Virginia, USA

International Nuclear Information System (INIS)

Levitan, Denise M.; Schreiber, Madeline E.; Seal, Robert R.; Bodnar, Robert J.; Aylor, Joseph G.

2014-01-01

Highlights: • We outline protocols for baseline geochemical surveys of stream sediments and water. • Regression on order statistics was used to handle non-detect data. • U concentrations in stream water near this unmined ore were below regulatory standards. • Concentrations of major and trace elements were correlated with stream discharge. • Methods can be applied to other extraction activities, including hydraulic fracturing. - Abstract: In this study, we determined baseline geochemical conditions in stream sediments and surface waters surrounding an undeveloped uranium deposit. Emphasis was placed on study design, including site selection to encompass geological variability and temporal sampling to encompass hydrological and climatic variability, in addition to statistical methods for baseline data analysis. The concentrations of most elements in stream sediments were above analytical detection limits, making them amenable to standard statistical analysis. In contrast, some trace elements in surface water had concentrations that were below the respective detection limits, making statistical analysis more challenging. We describe and compare statistical methods appropriate for concentrations that are below detection limits (non-detect data) and conclude that regression on order statistics provided the most rigorous analysis of our results, particularly for trace elements. Elevated concentrations of U and deposit-associated elements (e.g. Ba, Pb, and V) were observed in stream sediments and surface waters downstream of the deposit, but concentrations were below regulatory guidelines for the protection of aquatic ecosystems and for drinking water. Analysis of temporal trends indicated that concentrations of major and trace elements were most strongly related to stream discharge. These findings highlight the need for sampling protocols that will identify and evaluate the temporal and spatial variations in a thorough baseline study

The aqueous solubility and speciation analysis for uranium, neptunium and selenium by the geochemical code(EQ3/6)

International Nuclear Information System (INIS)

Takeda, Seiji; Shima, Shigeki; Kimura, Hideo; Matsuzuru, Hideo

1995-11-01

The geochemical condition of a geologic disposal system of HLW controls the solubility and physicochemical forms of dominant aqueous species for elements, which are one of essential information required for safety assessment. Based on the measured compositions of groundwater, the compositions of groundwater in the disposal system were calculated. The solubility and speciation analyses for the polyvalent elements, uranium, neptunium, and selenium, were performed by the geochemical code EQ3/6. The results obtained were compared with the data appeared in the literatures on the solubilities and speciations. The geochemical behaviors of the elements with respect to the solubility and speciation could quantitatively be elucidated for the compositions of the interstitial waters in an engineered barrier and ground water in a natural barrier. In the pH range of neutral to alkali, the solubilities of U and Np tend to increase with an increase of the carbonate concentration in groundwater. This carbonate concentration dependence of the solubility was also estimated. In the engineered barrier the predominant aqueous species were specified, and in the natural barrier the change of aqueous species was also predicted while the chemical compositions changed from the reducing to oxidizing conditions. The dominant aqueous species for the elements, which migrate in and through the disposal system, were determined by the speciation analysis. (author)

Quality assurance and quality control of geochemical data—A primer for the research scientist

Science.gov (United States)

Geboy, Nicholas J.; Engle, Mark A.

2011-01-01

Geochemistry is a constantly expanding science. More and more, scientists are employing geochemical tools to help answer questions about the Earth and earth system processes. Scientists may assume that the responsibility of examining and assessing the quality of the geochemical data they generate is not theirs but rather that of the analytical laboratories to which their samples have been submitted. This assumption may be partially based on knowledge about internal and external quality assurance and quality control (QA/QC) programs in which analytical laboratories typically participate. Or there may be a perceived lack of time or resources to adequately examine data quality. Regardless of the reason, the lack of QA/QC protocols can lead to the generation and publication of erroneous data. Because the interpretations drawn from the data are primary products to U.S. Geological Survey (USGS) stakeholders, the consequences of publishing erroneous results can be significant. The principal investigator of a scientific study ultimately is responsible for the quality and interpretation of the project's findings, and thus must also play a role in the understanding, implementation, and presentation of QA/QC information about the data. Although occasionally ignored, QA/QC protocols apply not only to procedures in the laboratory but also in the initial planning of a research study and throughout the life of the project. Many of the tenets of developing a sound QA/QC program or protocols also parallel the core concepts of developing a good study: What is the main objective of the study? Will the methods selected provide data of enough resolution to answer the hypothesis? How should samples be collected? Are there known or unknown artifacts or contamination sources in the sampling and analysis methods? Assessing data quality requires communication between the scientists responsible for designing the study and those collecting samples, analyzing samples, treating data, and

Geochemical prospecting for uranium and thorium deposits

International Nuclear Information System (INIS)

Boyle, R.W.

1980-01-01

A brief review of analytical geochemical prospecting methods for uranium and thorium is given excluding radiometric techniques, except those utilized in the determination of radon. The indicator (pathfinder) elements useful in geochemical surveys are listed for each of the types of known uranium and thorium deposits; this is followed by sections on analytical geochemical surveys based on rocks (lithochemical surveys), unconsolidated materials (pedochemical surveys), natural waters and sediments (hydrochemical surveys), biological materials (biogeochemical surveys) and gases (atmochemical surveys). All of the analytical geochemical methods are applicable in prospecting for thorium and uranium, particularly where radiometric methods fail due to attenuation by overburden, water, deep leaching and so on. Efficiency in the discovery of uranium and/or thorium orebodies is promoted by an integrated methods approach employing geological pattern recognition in the localization of deposits, analytical geochemical surveys, and radiometric surveys. (author)

Geochemical approach to evaluate deforest of mangroves

OpenAIRE

Ishiga, Hiroaki; Diallo, Ibrahima M'bemba; Bah Mamadou Lamine Malick,; Ngulimi. Faustine Miguta,; Magai. Paschal Justin,; Shati Samwel Stanley,

2016-01-01

Processes of mangrove deforest related human activities were examined. To evaluate changes of soil feature, multielements geochemical compositions of mangrove muds and soils of deforest were analyzed. To describe present situation of the mangrove, Conakry in Guinea, Dar es Salaam in Tanzania, Sundarbans of Bangladesh and Nago in Okinawa of Japan were selected. Soil samples of the forests were evaluated enrichment of biologically concentrated heavy metals such as Zn, Cu and Fe, and TS (total s...

Geochemical studies of backfill aggregates, lake sediment cores and the Hueco Bolson Aquifer

Science.gov (United States)

Thapalia, Anita

This dissertation comprises of three different researches that focuses on the application of geochemistry from aggregates, lake sediment cores and Hueco Bolson Aquifer. Each study is independent and presented in the publication format. The first chapter is already published and the second chapter is in revision phase. Overall, three studies measure the large scale (field) as well as bench scale (lab) water-rock interactions influenced by the climatic and anthropogenic factors spans from the field of environmental geology to civil engineering. The first chapter of this dissertation addresses the chemical evaluation of coarse aggregates from six different quarries in Texas. The goal of this work is to find out the best geochemical methods for assessing the corrosion potential of coarse aggregates prior to their use in mechanically stabilized earth walls. Electrochemical parameters help to define the corrosion potential of aggregates following two different leaching protocols. Testing the coarse and fine aggregates demonstrate the chemical difference due to size-related kinetic leaching effects. Field fines also show different chemistry than the bulk rock indicating the weathering impact on carbonate rocks. The second chapter investigates zinc (Zn) isotopic signatures from eight lake sediment cores collected both from pristine lakes and those impacted by urban anthropogenic contamination. Zinc from the natural weathering of rocks and anthropogenic atmospheric pollutants are transported to these lakes and the signatures are recorded in the sediments. Isotopic analysis of core samples provides the signature of anthropogenic contamination sources. Dated sediment core and isotopic analysis can identify Zn inputs that are correlated to the landuse and population change of the watersheds. Comparison of isotopic data from both pristine and urban lake sediment core also serves as an analog in other lake sediment cores in the world. The third chapter studies on Hueco Bolson

Geochemical and geophysical investigations, and fluid inclusion studies in the exploration area of Zafarghand (Northeast Isfahan, Iran

Directory of Open Access Journals (Sweden)

Zahra Alaminia

2017-11-01

Full Text Available Introduction Urumieh-Dokhtar Magmatic Arc (UDMA is a good prospective area for Cu, Cu-Mo and Cu-Au deposits (Fig. 1A and B. The Zafarghand district is located in the central part of the UDMA and the northeastern Isfahan. The present study concerns geological observations, alteration investigations, geochemical data and fluid inclusion studies. The purpose of the research is to identify geochemical anomalies and source of metals in this area. Geochemical anomalies for mineralizing elements and element associations were identified by using statistical analysis methods. Additionally, these results together suggest a site for exploration drilling in this study area. Materials and methods We collected 186 samples (rock along multi-cross sections oriented perpendicular to the strike of the South -Ardestan fault (Fig. 2.Trace element concentrations were determined by the ICP-MS technique in Amdel laboratory (Australia. Thin sections and doubly polished sections (100–200 µm thick from quartz veins were prepared from samples collected from the Zafarghand district in the University of Isfahan. Heating and freezing experiments on fluid inclusions were performed as defined (by Goldstein and Reynolds (1994 on a Linkam THM600 stage. Results Igneous rocks in the Zafarghand area are dominated by the Eocene and post Eocene acidic-intermediate rocks that include dacite, rhyodacite and andesite associated with diorite, quartz diorite and microdiorite intrusions. The present investigations indicate that all rocks of the Zafarghand district exhibit a variety of alterations. Hydrothermal alterations include phyllic, potassic, silicification, and argillic with widespread propylitic. The mineralization consists of malachite, azurite, hematite, and goethite, rare amounts of magnetite, pyrite, and chalcopyrite. Numerical traditional statistical analysis techniques have been applied to interpret the geochemical data of the study area. These methods are aimed at

Analysis of Regularly and Irregularly Sampled Spatial, Multivariate, and Multi-temporal Data

DEFF Research Database (Denmark)

Nielsen, Allan Aasbjerg

1994-01-01

This thesis describes different methods that are useful in the analysis of multivariate data. Some methods focus on spatial data (sampled regularly or irregularly), others focus on multitemporal data or data from multiple sources. The thesis covers selected and not all aspects of relevant data......-variograms are described. As a new way of setting up a well-balanced kriging support the Delaunay triangulation is suggested. Two case studies show the usefulness of 2-D semivariograms of geochemical data from areas in central Spain (with a geologist's comment) and South Greenland, and kriging/cokriging of an undersampled...... are considered as repetitions. Three case studies show the strength of the methods; one uses SPOT High Resolution Visible (HRV) multispectral (XS) data covering economically important pineapple and coffee plantations near Thika, Kiambu District, Kenya, the other two use Landsat Thematic Mapper (TM) data covering...

Geochemical and biogeochemical investigations in national parks [Badania geochemiczne i biogeochemiczne w parkach narodowych

Science.gov (United States)

Migaszewski, Z.M.; Lamothe, P.J.; Crock, J.G.

1998-01-01

National parks hold a key position among nature protection areas including a diversity of resources - natural, cultural, recreational and scenic. These "inviolable sanctuaries" are simultaneosuly ecologic knots and pristine nature refuges due to the presence of a number of unique plant and animal species. These species make up a natural gene bank. Classically, the level of biologic degradation in national parks is determined on the basis of qualitative and quantitative studies of plant bioindicators. Their scope encompasses phytosociologic survey the purpose of which is to identify floral assemblages with a detailed list of species to record future changes in their number. The best biomonitors of air quality are epiphytic lichens, ground mosses and conifers. Geochemical and biogeochemical investigations are widely performed in the U.S.A. to evaluate the degree of pollution in the nature protection areas including national parks (Gough et al., 1988a, b; Crock et al., 1992a, 1993; Jackson et al., 1995). Variability of element concentrations in soils and plants is assessed by using unbalanced, nested analysis-of-variance (ANOVA). It enables obtaining important statistical information with a minimum number of samples. In some cases a combined grid and barbell sampling design is applied (Jackson et al., 1995). In specific mountainous parks a method of 2-3 transects parallel to the extent of range (crest) is recommended. To determine the impact of a single pollution source on a given park, traverse sampling beginning near the emitter is used (Crock et al., 1992, 1993). The obtained results are a "snapshot" of chemical composition of soils and plant bioindicators that can be a reference for any future changes in the concentration level of chemical elements and organics. In addition, baseline element and organics composition of the media mentioned above can be compared with that obtained for geochemical atlases of polluted urban and industrial areas. Geochemical and

Geochemical fingerprints by activation analysis of tephra layers in Lake Van sediments, Turkey

Energy Technology Data Exchange (ETDEWEB)

Landmann, Guenter [Technische Universitaet Darmstadt, Institut fuer Angewandte Geowissenschaften, Schnittspahnstr. 9, 64287 Darmstadt (Germany); Steinhauser, Georg; Sterba, Johannes H. [Vienna University of Technology, Atominstitut, Stadionallee 2, 1020 Vienna (Austria); Kempe, Stephan [Technische Universitaet Darmstadt, Institut fuer Angewandte Geowissenschaften, Schnittspahnstr. 9, 64287 Darmstadt (Germany); Bichler, Max, E-mail: bichler@ati.ac.a [Vienna University of Technology, Atominstitut, Stadionallee 2, 1020 Vienna (Austria)

2011-07-15

We discuss geochemical and sedimentological characteristics of 12 tephra layers, intercalated within the finely laminated sediments of Lake Van. Within the about 15 kyr long sediment record studied, volcanic activity concentrated in the periods 2.6-7.2 and 11.9-12.9 kyr B.P. Concentrations of 25 elements provide the geochemical fingerprint of each tephra layer and allow comparison to literature values of potential source volcanoes such as Mts. Nemrut and Suephan. The youngest two tephra layers (and probably also the other three ashes from the 2.6-7.2 kyr B.P. eruptions) originate from the Nemrut volcano. The source of the older tephra (11.9-12.9 kyr B.P.), however, remains unidentified.

Geochemical maps of stream sediments in central Colorado, from New Mexico to Wyoming

Science.gov (United States)

Eppinger, Robert G.; Giles, Stuart A.; Klein, Terry L.

2015-01-01

The U.S. Geological Survey has completed a series of geologic, mineral resource, and environmental assessment studies in the Rocky Mountains of central Colorado, from Leadville eastward to the range front and from New Mexico to the Wyoming border. Regional stream-sediment geochemical maps, useful for assessing mineral resources and environmental effects of historical mining activities, were produced as part of the study. The data portrayed in this 56-parameter portfolio of landscape geochemical maps serve as a geochemical baseline for the region, indicate element abundances characteristic of various lithologic terranes, and identify gross anthropogenic effects of historical mining. However, although reanalyzed in this study by modern, sensitive methods, the majority of the stream-sediment samples were collected in the 1970s. Thus, metal concentrations portrayed in these maps represent stream-sediment geochemistry at the time of collection.

Appliance of geochemical engineering in radioactive waste disposal

International Nuclear Information System (INIS)

Li Shuang; Zhang Chengjiang; Ni Shijun; Li Kuanliang

2008-01-01

The basic foundation of applying geochemical engineering to control environment, common engineering models of disposal radioactive waste and the functions of the engineering barriers are introduced in this paper. The authors take the geochemical engineering barrier materiel research of a radioactive waste repository as an example to explain the appliance of geochemical engineering in the disposal of radioactive waste. And the results show that it can enhance the security of the nuclear waste repository if we use geochemical engineering barrier. (authors)

Effect of source integration on the geochemical fluxes from springs

International Nuclear Information System (INIS)

Frisbee, Marty D.; Phillips, Fred M.; White, Art F.; Campbell, Andrew R.; Liu, Fengjing

2013-01-01

Geochemical fluxes from watersheds are typically defined using mass-balance methods that essentially lump all weathering processes operative in a watershed into a single flux of solute mass measured in streamflow at the watershed outlet. However, it is important that we understand how weathering processes in different hydrological zones of a watershed (i.e., surface, unsaturated, and saturated zones) contribute to the total geochemical flux from the watershed. This capability will improve understanding of how geochemical fluxes from these different zones may change in response to climate change. Here, the geochemical flux from weathering processes occurring solely in the saturated zone is investigated. This task, however, remains exceedingly difficult due to the sparsity of subsurface sampling points, especially in large, remote, and/or undeveloped watersheds. In such cases, springflow is often assumed to be a proxy for groundwater (defined as water residing in fully saturated geologic formations). However, springflow generation may integrate different sources of water including, but not limited to, groundwater. The authors’ hypothesis is that long-term estimates of geochemical fluxes from groundwater using springflow proxies will be too large due to the integrative nature of springflow generation. Two conceptual models of springflow generation are tested using endmember mixing analyses (EMMA) on observations of spring chemistries and stable isotopic compositions in a large alpine watershed in the San Juan Mountains of southwestern Colorado. In the “total springflow” conceptual model, springflow is assumed to be 100% groundwater. In the “fractional springflow” conceptual model, springflow is assumed to be an integration of different sources of water (e.g., groundwater, unsaturated flow, preferential flow in the soil, etc.) and groundwater is only a fractional component. The results indicate that groundwater contributions in springflow range from 2% to 100

Analysis of the potential impact of capillarity on long-term geochemical processes in sulphidic waste-rock dumps

International Nuclear Information System (INIS)

Pedretti, Daniele; Lassin, Arnault; Beckie, Roger D.

2015-01-01

Highlights: • Capillarity may affect geochemical reactions generating acid-rock drainage. • We studied its impact in a simplified, synthetic WRD. • Capillarity mainly affects the formation of secondary minerals. • It can strongly control long-term formation of gypsum and in turn sulfate release. • Capillarity can be also important for the analysis of calcite passivation. - Abstract: Assessing long-term production of acid rock drainage (ARD) from waste-rock dumps (WRDs) requires a careful analysis of the processes controlling acid-generating geochemical reactions under unsaturated conditions. In this work, we focus on the potential control of capillarity on these reactions, as previous studies showed that capillarity affects the activity of water and solutes in the unsaturated zone through the pore water pressure. We used capillarity-corrected thermodynamic databases and compared calculated speciation and solubility results with those from databases that do not account for capillarity. We developed a simple dynamic model with reduced geochemical components to analyze in detail the effect of capillarity. Results indicate that under low pH conditions simulations with capillarity-controlled reactions generate relatively larger dissolved sulfate concentrations from the WRDs over longer time scales, when compared against simulations without capillarity control. This occurs because capillarity strongly controls the formation of secondary sulfate-bearing minerals such as gypsum. When sufficient oxygen and carbon dioxide partial pressures are maintained within WRDs (such as in well-ventilated systems) and calcite content is insufficient to buffer acidity, the amount of secondary gypsum was calculated to be much larger in capillarity-corrected models. No appreciable effects of capillarity were observed under conditions where gypsum was not generated. Model results are also insensitive to temperature changes in typical climatic ranges. These results indicate some of

Regional geochemical prospecting of uranium in the Amazon region

International Nuclear Information System (INIS)

Zenker, A.O.; Hohn, H.

1982-01-01

A regional geochemical prospecting program for uranium in the Serra dos Carajas area, south of Para, was performed by NUCLEBRAS using stream sediment samples obtained from other companies acting in this area. The results of the survey are presented compared to regional geology and an aerial total count map. The different data showed a good correlation, particularly in areas mapped regionally as granitic rocks. (Author) [pt

Establishing nursery estuary otolith geochemical tags for Sea Bass (Dicentrarchus labrax): Is temporal stability estuary dependent?

Science.gov (United States)

Ryan, Diarmuid; Wögerbauer, Ciara; Roche, William

2016-12-01

The ability to determine connectivity between juveniles in nursery estuaries and adult populations is an important tool for fisheries management. Otoliths of juvenile fish contain geochemical tags, which reflect the variation in estuarine elemental chemistry, and allow discrimination of their natal and/or nursery estuaries. These tags can be used to investigate connectivity patterns between juveniles and adults. However, inter-annual variability of geochemical tags may limit the accuracy of nursery origin determinations. Otolith elemental composition was used to assign a single cohort of 0-group sea bass Dicentrarchus labrax to their nursery estuary thus establishing an initial baseline for stocks in waters around Ireland. Using a standard LDFA model, high classification accuracies to nursery sites (80-88%) were obtained. Temporal stability of otolith geochemical tags was also investigated to assess if annual sampling is required for connectivity studies. Geochemical tag stability was found to be strongly estuary dependent.

Geochemical evidence for mixing of three components in martian orthopyroxenite ALH 84001. [Abstract only

Science.gov (United States)

Mittlefehldt, D. W.; Lindstrom, M. M.

1994-01-01

ALH 84001, a ferroan martian orthopyroxenite, originally consisted of three petrographically defined components: a cumulus assemblage of orthopyroxene + chromite, a trapped melt assemblage of orthopyroxene(?) + chromite + maskelynite + apatite + augite +/- pyrite, and a metasomatic assemblage of carbonate +/- pyrite. We present the results of Instrumental Neutron Activation Analysis (INAA) study of five bulk samples of ALH 84001, combined with Scanning Ion Mass Spectrometer (SIMS) data on the orthopyroxene, in order to attempt to set limits on the geochemical characteristics of the latter two components, and therefore on the petrogenesis of ALH 84001. The INAA data support the petrographic observations, suggesting that there are at least three components in ALH 84001. We will assume that each of the three geochemically required components can be equated with one of the petrographically observed components. Both trapped melt and metasomatic components in ALH 84001 have higher Na than orthopyroxene based on compositions of maskelynite, apatite, and carbonate. For the metasomatic component, we will assume its Na content is that of carbonate, while for a trapped melt component, we will use a typical Na content inferred for martian meteorite parent melts, approximately 1 wt% Na2O. Under these assumptions, we can set limits on the Light Rare Earth Elements/Heavy Rare Earth Elements (LREE/HREE) ratios of the components, and use this information to compare the petrogenesis of ALH 84001 with other martian meteorites. The above calculations assume that the bulk samples are representative of different portions of ALH 84001. We will also evaluate the possible heterogeneous distribution of mineral phases in the bulk samples as the cause of compositional heterogeneity in our samples.

Geochemical modeling: a review

International Nuclear Information System (INIS)

Jenne, E.A.

1981-06-01

Two general families of geochemical models presently exist. The ion speciation-solubility group of geochemical models contain submodels to first calculate a distribution of aqueous species and to secondly test the hypothesis that the water is near equilibrium with particular solid phases. These models may or may not calculate the adsorption of dissolved constituents and simulate the dissolution and precipitation (mass transfer) of solid phases. Another family of geochemical models, the reaction path models, simulates the stepwise precipitation of solid phases as a result of reacting specified amounts of water and rock. Reaction path models first perform an aqueous speciation of the dissolved constituents of the water, test solubility hypotheses, then perform the reaction path modeling. Certain improvements in the present versions of these models would enhance their value and usefulness to applications in nuclear-waste isolation, etc. Mass-transfer calculations of limited extent are certainly within the capabilities of state-of-the-art models. However, the reaction path models require an expansion of their thermodynamic data bases and systematic validation before they are generally accepted

Geochemical modeling: a review

Energy Technology Data Exchange (ETDEWEB)

Jenne, E.A.

1981-06-01

Two general families of geochemical models presently exist. The ion speciation-solubility group of geochemical models contain submodels to first calculate a distribution of aqueous species and to secondly test the hypothesis that the water is near equilibrium with particular solid phases. These models may or may not calculate the adsorption of dissolved constituents and simulate the dissolution and precipitation (mass transfer) of solid phases. Another family of geochemical models, the reaction path models, simulates the stepwise precipitation of solid phases as a result of reacting specified amounts of water and rock. Reaction path models first perform an aqueous speciation of the dissolved constituents of the water, test solubility hypotheses, then perform the reaction path modeling. Certain improvements in the present versions of these models would enhance their value and usefulness to applications in nuclear-waste isolation, etc. Mass-transfer calculations of limited extent are certainly within the capabilities of state-of-the-art models. However, the reaction path models require an expansion of their thermodynamic data bases and systematic validation before they are generally accepted.

Geochemical of trace elements in volcanics rocks Peninsula Fildes, Fildes Bay Rey Jorge island, south Shetland

International Nuclear Information System (INIS)

Masquelin, H.; Vaz Chavez, N.

1987-01-01

The authors present some geochemical data derived from the multielement analysis of three different types of volcanic rocks collected around Fildes Bay on King George Island, South Shetland. Volcanic rocks from Fildes Peninsula Group may be distinguished from those Marian Cove by their hydrothermal alteration. Apparently the correlation between NI ands Cr allows for the observation of the stratigraphic separation of samples of the same kind. Consequently, the correlation between Cu and As show a distinction between Marian Cove propylitised tuffites and both Brecciated Andesites and pyroclastic rock from Fildes Peninsula Group.

NOAA and MMS Marine Minerals Geochemical Database

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — The Marine Minerals Geochemical Database was created by NGDC as a part of a project to construct a comprehensive computerized bibliography and geochemical database...

A preliminary study on the geochemical environment for deep geological disposal of high level radioactive waste in Korea

International Nuclear Information System (INIS)

Kim, Chun Soo; Bae, Dae Seok; Kim, Kyung Su; Koh, Yong Kwon; Park, Byoung Yun

2000-03-01

Geochemical study on the groundwater from crystalline rocks (granite and gneiss) for the deep geological disposal of high-level radioactive waste was carried out in order to elucidate the hydrogeochemical and isotope characteristics and geochemical evolution of the groundwater. Study areas are Jungwon, Chojeong, Youngcheon and Yusung for granite region, Cheongyang for gneiss region, and Yeosu for volcanic region. Groundwaters of each study areas weree sampled and analysed systematically. Groundwaters can be grouped by their chemistry and host rock. Origin of the groundwater was proposed by isotope ( 18 O, 2 H, 13 C, 34 S, 87 Sr, 15 N) studies and the age of groundwater was inferred from their tritium contents. Based ont the geochemical and isotope characteristics, the geochemical evolutions of each types of groundwater were simulated using SOLVEQ/CHILLER and PHREEQC programs

Instrumental neutron and photon activation analyses of selected geochemical reference materials

Czech Academy of Sciences Publication Activity Database

Mizera, Jiří; Řanda, Z.

2010-01-01

Roč. 284, č. 1 (2010), s. 157-163 ISSN 0236-5731 Institutional research plan: CEZ:AV0Z30460519 Keywords : neutron activation analysis * photon activation analysis * geochemical reference materials Subject RIV: BG - Nuclear, Atomic and Molecular Physics, Colliders OBOR OECD: Analytical chemistry Impact factor: 0.777, year: 2010

Similarity in Evolutionary Histories of Eocene Sediments from Subathu and Cambay Basins: Geochemical and Palaeontological Studies

Science.gov (United States)

Chaudhuri, S.; Halder, K.; Sarkar, S.

2017-12-01

A systematic comparative study of microfaunal assemblage and representative geochemical elements from two Cenozoic basins of India, Mangrol-Valia Lignite Mine section (21°30'52''N:73°12'20.5''E) of Cambay Shale Formation, western India and Jigni section (33°14'45"N:74°22'0"E) from Subathu Formation in northern India was undertaken to infer the paleoenvironment, palaeobathymetry and paleoclimate of these successions. Despite a gamut of work already carried out in these two basins, the sedimentary successions still await a correlative-detailed process-based facies, geochemical characterization and paleoenvironmental analysis. With a view to fulfill this gap, the present work was carried out by studying bulk rock XRD, XRF, clay mineralogy and analyzing calcareous microfossil foraminifera from samples at equivalent depth of these two basins which are situated thousands of kilometers apart and in different tectonic settings. The faunal assemblage of Eocene sediments of Mangrol-Valia section is indicative of shallow marine and inner shelf deposition with medium oxygen supply, while that of the Jigni section suggests primarily a shallow marine condition, which gradually changes to open marine condition with time. It is pertinent to note that the two basins of Cenozoic India started their lithosuccession with coal bearing strata. Well preserved pectin aragonite shells also indicate that primarily these two basins experienced low energy lagoonal environment. The fossil assemblage in both basins also suggests a tropical moist to terrestrial lowland environment. Geochemical analysis shows that the Mangrol-Valia section mineralogically comprises of kaolinite, siderite, quartz, smectite and kaolinite with higher abundance throughout the succession indicating chemical weathering of Deccan basement and high erosional environment. Calcite is the main constituent of Jigni section that indicates intracratonic rift settings. Medium to high quartz content and other detrital

Late Cambrian magmatic arc activity in peri-Gondwana: geochemical evidence from the Basal Allochthonous Units of NW Iberia

Energy Technology Data Exchange (ETDEWEB)

Andonaegui, P.; Abati, J.; Díez-Fernández, R.

2017-07-01

The North African section of the Gondwana margin was the site of voluminous, arc-related magmatism during the Late Neoproterozoic (Avalonian–Cadomian orogen). The lower (and older) metasedimentary sequence that constitutes the Basal Units of the Allochthonous Complexes of NW Iberia was deposited in that setting. In these units, sedimentation was followed by the intrusion of tonalites and granodiorites in the late Cambrian (ca. 493–489Ma). In the Late Paleozoic, the collision of Gondwana and Laurussia (Variscan orogeny) deformed and metamorphosed the whole ensemble. New whole rock geochemical analysis performed in seven samples of metatonalites and fourteen samples of metagranodiorites are characterized by: i) slight enrichment in incompatible elements (Rb, Ba, Th, U), ii) negative anomalies in Nb, Ta, P, and Ti, and iii) negative anomalies in Eu. These chemical features are in agreement with a subduction-related setting for the genesis of both types of magma, which is also supported by chemical discrimination using tectonic setting diagrams. Positive anomalies of Pb suggest a crustal component. The new geochemical data reveal that the convergent orogen that ruled the paleogeography of the Gondwana periphery during the Neoproterozoic (Cadomian orogen) remained active bey.

Petrological mineralogical and geochemical characterization of the granitoids and fracture fillings developed in Ratones Mines (Spain)

International Nuclear Information System (INIS)

Buil Gutierrez, B.

2002-01-01

The petrological, mineralogical and geochemical characterisation of the granitoids and fracture fillings developed in the Ratones Mine (Caceres, Spain) has been done in order to understand rock-water interaction processes which control water geochemical parameters. Special interest has been devoted to the analysis and interpretation of REE patterns in the solid phase (granitoids and fracture fillings) because they constitute geochemical tracers in water-rock interaction process. Moreover, REE are considered as actinide analogues. In order to characterise the solid phase (granitoids and fracture fillings) several investigation scales (system, outcrop, whole rock, mineral and geochemical components) have been considered and different types of samples have been analysed. These factors control the methodological approach used in this investigation. The analytical methods we have used in this investigation are microscope, qualitative and semi-quantitative methods (XRD, SEM,EDAX) and quantitative methods (ICP-MS, XRF, EM, LAM-IC-MS). The bulk of the granitoids located around the Ratones Mine Belongs to the alkaline feldspar granite-sienogranite lihotype and they show a peraluminous and subalkaline pattern. From the mineralogical point of view, they are composed by quartz, K-feldspar (Or>90%), showing sericitation, moscovitization and turmolinization altherations, alkaline plagioclase (An-=-3%), usually altered to sericite, saussirite and less frequently affected by moscovitization processes, Fe-Al biotite, frequently affected by chloritization processes and sometimes replaced by muscovite, and finally muscovite (>2% celadonite and <4% paragonite) both of primary and secondary origin. The differences observed between the different lithotypes are related with the modal proportion of the principal minerals,with the presence or absence of certain accessory minerals ( turmaline, cordierite), with specific textural patterns, grain size and also with the richness in specific

Geochemical Characterization of the Upper and Middle Floridan Aquifer System, South Florida

Science.gov (United States)

Mirecki, J.; Richardson, E.; Bennett, M.; Hendel, J.

2008-05-01

Our study focus is to characterize the water quality and geochemical environment of the Floridan Aquifer System (FAS) throughout the regional flowpath. A synoptic survey of 21 wells (n=15, upper FAS; n=6 middle FAS) was supplemented by additional samples (n=11) obtained during exploratory well development at 4 aquifer storage recovery (ASR) pilot sites. Synoptic survey samples were analyzed intensively, yielding a dataset that consists of major and trace dissolved constituents (including metals), stable isotopes (δ18O, δ13C, δD, δ34S in sulfate and sulfide), carbon species (carbonate alkalinity and organic carbon), uranium-series radionuclides, nutrients, and selected microbes and pathogens. The objectives of this study are three-fold: 1) to provide baseline water-quality and geochemical information prior to initiation of ASR activities that are part of the Comprehensive Everglades Restoration Plan; 2) to quantify the major controls on geochemical evolution along upper and middle FAS flowpaths using geochemical modeling methods; and 3) to identify areas where water- quality may limit the feasibility of ASR methods in the FAS. Preliminary interpretations water quality changes along the regional FAS flowpath can be summarized as follows. Concentrations of dissolved constituents increase from north to south along the flow path; generally, the upper FAS has lower total dissolved solids than the middle FAS at locations where well pairs were analyzed. The redox environment changes from oxic to strongly anoxic, very close to the recharge area. Redox measurements, dissolved iron, sulfide, and sulfur isotope data are consistent with sulfate-reducing conditions. Uranium-series isotope concentrations and activities generally are below regulatory criteria, with few exceptions in both the upper and middle FAS. Areas with greater radionuclide activity occur primarily at distal flowpath locations or at the coast.

Integration of remote sensing and geochemical data in the mineral evaluation of the Yucca Mountain Addition, Nevada

International Nuclear Information System (INIS)

Feldman, S.C.; Castor, S.B.; Tingley, J.V.

1996-01-01

In 1989 the U.S. Department of Energy filed an application with the U.S. Bureau of Land Management for an administrative land withdrawal of about 4,300 acres bordering the western edge of the Nevada Test Site (NTS) and the southern edge of the Nellis Air Force Range. This area, which is referred to as the Yucca Mountain Addition, includes approximately 400 acres that are being considered as part of a potential repository for high-level nuclear waste at Yucca Mountain. A study of the geology and mineral deposits is required for a land withdrawal request under federal law. The Yucca Mountain Addition mineral evaluation was accomplished in late 1989 by field examination, sample collection, geochemical analysis, the analysis of satellite remote sensing data, and the collection of rock spectra in the field. Data from the Yucca Mountain Addition and from mining districts in the area were collected and analyzed, and the two data sets were then compared. The evaluation was limited to surficial data both at the Yucca Mountain Addition and in the mining districts. Evidence from both geochemical and remote sensing analyses indicate that the potential for mineral deposits is low in the Yucca Mountain Addition

Geochemical Investigation of Clay Minerals in Marte, Borno State, Nigeria

Directory of Open Access Journals (Sweden)

F. D. Adams

2017-10-01

Full Text Available Clay deposit collected from various locations in Marte (Northern Borno, were studied to determine their physical and chemical characteristics in order to evaluate their suitability for industrial uses. Major and trace element analyses were carried out on clay samples using Inductively Couple Plasma-Optical Emission Spectrometry (ICP-OES and X- Ray Fluorescence (XRF. The result of the chemical analysis of the ten (10 samples collected showed significant amounts of SiO2 and Al2O3. Silica content ranges from 51.48 to 62.44 % while alumina varies from 12.49 to 19.00 %. The calcium oxide ranges from 1.17 to 3.39 %, Na2O ranges from 1.1 to 8.61 %, K2O from 1.54 to 3.66 %, MgO varies from 0.04 to0.14 %, Fe2O3 varies from 0.3 to 2.7 % and MnO ranges from 0.01 to 1.03 %. The result showed that the clays are mainly smectite with quartz and felspar as the main non-clay minerals. Generally, the geochemical results of the samples do not meet the standard for industrial utilization when compared to the Industrial specifications. However, for industrial utilization, some of the clay samples may be used after necessary beneficiations.

Geochemical and mineralogical characteristics of Lithomargic clay

African Journals Online (AJOL)

Administrator

Geochemical and mineralogical characteristics of Lithomargic clay. GEOCHEMICAL AND .... tries, as filling material in the pulp and paper, toothpaste and paint industries as well ..... tions very vital to human health and other ac- tivities of man.

Environmental and geochemical studies using lower energy accelerator mass spectrometer

International Nuclear Information System (INIS)

Uchida, Masao; Kumata, Hidetoshi

2016-01-01

This paper introduces the latest versatile lower energy AMS, which shows a remarkable progress in recent years, the system incorporating it with a variety of analytical instruments, and environmental and geochemical studies using AMS associated with natural level "1"4C tracer, such as the analysis of Asian Brown Cloud originated from black carbon (BC) and the analysis of BC transport due to big rivers in the Arctic. Part of the lower energy AMS has been specifically developed for radiocarbon measurement. It has enabled, through a high-performance gas introduction interface system (GIS), the online introduction into the gas ion source of the sample gas that has been CO_2-converted with a pre-processing unit. Such online system achieved the simplification of sample pre-treatment, and a significant reduction (several μg-C to 1 mg-C) in necessary amount for analysis due to the above simplification. With the progress of such measurement techniques, the construction of "1"4CO_2 database on a global scale, which conventionally could not easily be realized, can be realized. From the observation data of "1"4CO_2, it is possible to more accurately grasp the amount of CO_2 released into the atmosphere through fossil fuel combustion. Therefore, the accuracy improvement of a numerical calculation model used for the estimation of CO_2 balance on earth can be expected. (A.O.)

Petrographic and geochemical data for Cenozoic volcanic rocks of the Bodie Hills, California and Nevada

Science.gov (United States)

du Bray, Edward A.; John, David A.; Box, Stephen E.; Vikre, Peter G.; Fleck, Robert J.; Cousens, Brian L.

2013-04-23

Petrographic and geochemical data for Cenozoic volcanic rocks of the Bodie Hills, California and Nevada // // This report presents petrographic and geochemical data for samples collected during investigations of Tertiary volcanism in the Bodie Hills of California and Nevada. Igneous rocks in the area are principally 15–6 Ma subduction-related volcanic rocks of the Bodie Hills volcanic field but also include 3.9–0.1 Ma rocks of the bimodal, post-subduction Aurora volcanic field. Limited petrographic results for local basement rocks, including Mesozoic granitoid rocks and their metamorphic host rocks, are also included in the compilation. The petrographic data include visual estimates of phenocryst abundances as well as other diagnostic petrographic criteria. The geochemical data include whole-rock major oxide and trace element data, as well as limited whole-rock isotopic data.

Quantitative study of Portland cement hydration by X-Ray diffraction/Rietveld analysis and geochemical modeling

Science.gov (United States)

Coutelot, F.; Seaman, J. C.; Simner, S.

2017-12-01

In this study the hydration of Portland cements containing blast-furnace slag and type V fly ash were investigated during cement curing using X-ray diffraction, with geochemical modeling used to calculate the total volume of hydrates. The goal was to evaluate the relationship between the starting component levels and the hydrate assemblages that develop during the curing process. Blast furnace-slag levels of 60, 45 and 30 wt.% were studied in blends containing fly ash and Portland cement. Geochemical modelling described the dissolution of the clinker, and predicted quantitatively the amount of hydrates. In all cases the experiments showed the presence of C-S-H, portlandite and ettringite. The quantities of ettringite, portlandite and the amorphous phases as determined by XRD agreed well with the calculated amounts of these phases after different periods of time. These findings show that changes in the bulk composition of hydrating cements can be described by geochemical models. Such a comparison between experimental and modelled data helps to understand in more detail the active processes occurring during cement hydration.

Geochemical dispersion of uranium near prospects in Pennsylvania

International Nuclear Information System (INIS)

Rose, A.W.; Schmiermund, R.L.; Mahar, D.L.

1977-06-01

The geochemical dispersion of U was investigated near sedimentary uranium prospects in eastern and north-central Pennsylvania. Near Jim Thorpe, known uranium occurrences in the Catskill Fm. are limited to the base of the Duncannon member. At Penn Haven Junction, roll-type U deposits with appreciable Pb and Se are localized adjacent to an oxidized tongue of channel-filling conglomeratic sandstone. The channel and encircling U occurrences furnish a large target for geochemical exploration. Selective extractions show that the organic, Fe-oxide, sand and silt fractions of stream sediments are the major hosts for U in stream sediments. Fe-oxides have a greater affinity for U than organic matter but are less abundant. The U content of organic matter is about 10 5 times the U content of stream water. Stream sediments furnish a representative sample of the average content of U, Zn, Cu, and major elements in soils of a drainage basin in north-central Pennsylvania, so a semiquantitative appraisal of weathering uranium occurrences can be made from stream sediments in climates and topography like Pennsylvania. The flux of uranium leaving the basin in solution is about equal to that leaving as sediment. Uranium is considerably less mobile than Ca and Na. A new method of extracting uranium from water samples, using a liquid ion exchanger (Amberlite LA-1), shows promise for simple field application

METHYL MERCURY PRODUCTION IN NATURAL-COLLECTED SEDIMENT WITH DIFFERENT GEOCHEMICAL PARAMETERS

Directory of Open Access Journals (Sweden)

Markus T. Lasut

2010-06-01

Full Text Available Production of methyl mercury (MeHg has been shown in laboratory experiments using mercuric chloride (HgCl2 compound released into natural-collected sediments with different geochemical conditions. While the HgCl2 concentration was 30 µl of 113 ppm of HgCl2, the geochemical conditions [pH, salinity, total organic content (TOC, sulfur] of sampled sediments were A: 8.20, 0.00 ppt, 1.97%, and 0.92 ppt, respectively; B: 7.90, 2.00 ppt, 4.69%, and 1.98 ppt, respectively; and C: 8.20, 24.00 ppt, 1.32 %, and 90.90 ppt, respectively. A control was set with no HgCl2. Samples and control were incubated in room temperature of 27 ± 1 °C. Observations were done along 9 days with interval of 3 days. While total Hg was measured using mercury analyzer with Cold Vapor-Atomic Absorbtion Spectrophometer (CV-AAS system, MeHg was measured by using a gas chromatograph with ECD detector after extracted by dithizone-sodium sulfide extraction method. The result shows that MeHg was found in both treatment and control experiments. The concentrations of the MeHg varied according to the geochemical condition of the sampled sediments. Peak production of MeHg occurred on the third day; however, the production was not significantly affected by the incubation time. Optimum production was found inversely related to the pH, in which highest and lowest the pH formed an ineffectively methylated mercury species. The TOC was significantly correlated to the optimum production. Salinity and sulfate contents were found not correlated to the optimum of MeHg production.   Keywords: Methyl mercury; methylation process; sediment; biogeochemistry

Proceedings of 13. International Geochemical Exploration Symposium. 2. Brazilian Geochemical Congress

International Nuclear Information System (INIS)

1989-01-01

Some works about geochemistry are presented, including themes about geochemical exploration, lithogeochemistry and isotope geochemistry, environmental geochemistry, analyical geochemistry, geochemistry of carbonatites and rare earth elements and organic geochemistry. (C.G.C.) [pt

A preliminary study on the geochemical environment for deep geological disposal of high level radioactive waste in Korea

Energy Technology Data Exchange (ETDEWEB)

Kim, Chun Soo; Bae, Dae Seok; Kim, Kyung Su; Koh, Yong Kwon; Park, Byoung Yun

2000-03-01

Geochemical study on the groundwater from crystalline rocks (granite and gneiss) for the deep geological disposal of high-level radioactive waste was carried out in order to elucidate the hydrogeochemical and isotope characteristics and geochemical evolution of the groundwater. Study areas are Jungwon, Chojeong, Youngcheon and Yusung for granite region, Cheongyang for gneiss region, and Yeosu for volcanic region. Groundwaters of each study areas weree sampled and analysed systematically. Groundwaters can be grouped by their chemistry and host rock. Origin of the groundwater was proposed by isotope ({sup 18}O, {sup 2}H, {sup 13}C, {sup 34}S, {sup 87}Sr, {sup 15}N) studies and the age of groundwater was inferred from their tritium contents. Based ont the geochemical and isotope characteristics, the geochemical evolutions of each types of groundwater were simulated using SOLVEQ/CHILLER and PHREEQC programs.

Evolved Gas Analyses of Sedimentary Materials in Gale Crater, Mars: Results of the Curiosity Rover's Sample Analysis at Mars (SAM) Instrument from Yellowknife Bay to the Stimson Formation

Science.gov (United States)

Sutter, B.; McAdam, A. C.; Rampe, E. B.; Ming, D. W.; Mahaffy, P. R.; Navarro-Gonzalez, R.; Stern, J. C.; Eigenbrode, J. L.; Archer, P. D.

2016-01-01

The Sample Analysis at Mars (SAM) instrument aboard the Mars Science Laboratory rover has analyzed 10 samples from Gale Crater. All SAM evolved gas analyses have yielded a multitude of volatiles (e.g, H2O, SO2, H2S, CO2, CO, NO, O2, HC1). The objectives of this work are to 1) Characterize the evolved H2O, SO2, CO2, and O2 gas traces of sediments analyzed by SAM through sol 1178, 2) Constrain sediment mineralogy/composition based on SAM evolved gas analysis (SAM-EGA), and 3) Discuss the implications of these results releative to understanding the geochemical history of Gale Crater.

Report on the geological-geochemical research carried out within the area of geochemical anomaly P7, Vathyrema, Drama Department

International Nuclear Information System (INIS)

Stavropoulos, Athanasios.

1982-08-01

The investigated area covering about 30 km 2 is situated in the crystalline massive of Rhodope (north of Drama deparment, E. Macedonia) where granitoids constitute its main petrological type. The geological-geochemical and radiometric investigations carried out so far in the area have localized a large number of places with high values of γ-radiation (1.000 - 15.000 c/s), as well as high concentrations of uranium (50-500 ppm). The uranium mineralization within the zone of oxidation is expressed by the uranium mineral autunite, accompanied by intensive hematitization-limonitization and chloritization-kaolinization, and additionally by small spots and veinlets of pyrite and galena. It seems that tectonic control exists on the uranium mineralization, since most of the anomalous concentrations of uranium are sitting along mylonite zones rich in chlorite and kaolin. There have been discerned seven more anomalous part areas which will have to be covered by geochemical stream sediment sampling (phase 3), as well as geological mapping (scale 1:5.000). The results from the research conducted within the concerned anomaly lead us to the conclusion that this area is very promising and possibilities of localization of uranium payable concentrations are very high. (N.Ch.)

Geochemical signatures of tephras from Quaternary Antarctic Peninsula volcanoes

OpenAIRE

Kraus,Stefan; Kurbatov,Andrei; Yates,Martin

2013-01-01

In the northern Antarctic Peninsula area, at least 12 Late Plelstocene-Holocene volcanic centers could be potential sources of tephra layers in the region. We present unique geochemical fingerprints for ten of these volcanoes using major, trace, rare earth element, and isotope data from 95 samples of tephra and other eruption products. The volcanoes have predominantly basaltic and basaltic andesitic compositions. The Nb/Y ratio proves useful to distinguish between volcanic centers located on ...

Field-based tests of geochemical modeling codes: New Zealand hydrothermal systems

International Nuclear Information System (INIS)

Bruton, C.J.; Glassley, W.E.; Bourcier, W.L.

1993-12-01

Hydrothermal systems in the Taupo Volcanic Zone, North Island, New Zealand are being used as field-based modeling exercises for the EQ3/6 geochemical modeling code package. Comparisons of the observed state and evolution of the hydrothermal systems with predictions of fluid-solid equilibria made using geochemical modeling codes will determine how the codes can be used to predict the chemical and mineralogical response of the environment to nuclear waste emplacement. Field-based exercises allow us to test the models on time scales unattainable in the laboratory. Preliminary predictions of mineral assemblages in equilibrium with fluids sampled from wells in the Wairakei and Kawerau geothermal field suggest that affinity-temperature diagrams must be used in conjunction with EQ6 to minimize the effect of uncertainties in thermodynamic and kinetic data on code predictions

Data for the geochemical investigation of UMTRAP designated site at Monument Valley, Arizona

International Nuclear Information System (INIS)

Markos, G.; Bush, K.J.

1983-09-01

This report contains the geochemical data and the methods of data collection from the former tailings site at Monument Valley, Arizona. Data are from a one-time sampling of waters and solid material from the background, the area adjacent to the site, and the site. Selected solid samples are water extracted to remove easily soluble salts. The waters and extracts of solid samples were analyzed for selected major and trace elements. 3 refs., 2 figs., 1 tab

Geochemical studies of the sediments of Barreiras group, Itaborai region-RJ, Brazil

International Nuclear Information System (INIS)

Neves, M.C.G.P.

1983-01-01

It is purpused to study the lead, copper, chromium, manganese, vanadium and zinc geochemical bahavior of the clays obtained from outcrop samples of Barreiras group and weathered Pre-Cambriam situated at Itaborai region, in Rio de Janeiro State, Brazil. Field and laboratory description, grain size analyses, X-ray diffraction, emission spectrography, X-ray fluorescence, atomic absorption, transmission electronic microscopy and pH tests were applied to twenty-two samples selected. (Author) [pt

Use of termite mounds in geochemical exploration in North Ethiopia [rapid communication

Science.gov (United States)

Kebede, Fassil

2004-09-01

The geochemistry of the termite mounds was studied in lower Giba River basin, Kolla Tambien district, northern Ethiopia to show that they are useful in searching for metals. Specimens from the termite mounds and parent materials were collected to quantify gold, silver, copper, zinc, cobalt, manganese, iron and nickel. The results of the geochemical analysis of the samples indicated that these metals exist both in the termite mound and the parent material in the surrounding area. Correlation analysis shows that termite mounds and the parent materials are positively correlated for gold ( r = 0.75∗), copper ( r = 0.77∗), silver ( r = 0.56∗) and manganese ( r = 0.72). This positive correlation leads to the conclusion that there is a direct relation between the concentration of metals in termite mound and the parent rocks. Termite mounds can therefore be used as tools in exploring for these metals.

Computer analysis to the geochemical interpretation of soil and stream sediment data in an area of Southern Uruguay

International Nuclear Information System (INIS)

Spangenberg, J.

2010-01-01

In southern Uruguay there are several known occurrences of base metal sulphide mineralization within an area of Precambrian volcanic sedimentary rocks. Regional geochemical stream sediment reconnaissance surveys revealed new polymetallic anomalies in the same stratigraphic zone. Geochemical interpretation of multi-element data from a soil and stream sediment survey carried out in one of these anomalous areas is presented.

Instrumental neutron and photon activation analyses of selected geochemical reference materials

Czech Academy of Sciences Publication Activity Database

Mizera, Jiří; Řanda, Zdeněk

2010-01-01

Roč. 284, č. 1 (2010), s. 157-163 ISSN 0236-5731 R&D Projects: GA AV ČR IAA300130706 Institutional research plan: CEZ:AV0Z10480505 Keywords : neutron activation analysis * photon activation analysis * geochemical reference materials Subject RIV: BG - Nuclear, Atomic and Molecular Physics, Colliders Impact factor: 0.777, year: 2010

Geochemical character of Southern African Kimberlites: a new approach based on isotopic constraints

International Nuclear Information System (INIS)

Smith, C.B.; Gurney, J.J.; Ebrahim, N.

1985-01-01

Major and trace element compositions of southern African kimberlite samples previously analysed for isotopic compositions confirm that isotopically defined Group I (basaltic) and Group II (micaceous) variants have distinctive geochemical signatures. These signatures are generally consistent with geochemical variation in petrographically defined types. Stepwise discriminant function analysis is used to define the most important geochemical distinctions at the group level and to derive a procedure which successfully classifies a large number of unknowns based on chemical composition only. In comparison to Group I, Group II kimberlites have consistently higher abundances of SiO 2 , K 2 O, Pb, Rb, Ba and LREE, and lower abundances of TiO 2 and Nb. In conjunction with isotopic results, the distinctions in incompatible element contents in particular are believed to reflect broad differences in source rock character. Results are consistent with derivation of Group I kimberlites from asthenospheric-like sources similar to those from which oceanic island basalts are produced. In contrast, Group II kimberlites are inferred to originate from sources within ancient stabilized subcontinental lithosphere characterized by time-averaged incompatible element enrichment. Group I kimberlites can be further subdivided into two isotopically similar types to some degree correlative with tectonic environment. Compared to subgroup IA (on-craton), IB kimberlites have lower SiO 2 and higher CaO, FeO + Fe 2 O 3 and volatile contents in addition to somewhat greater TiO 2 , P 2 O 5 , Nb, Zr and Y abundances, and tend to occur outside the inferred boundaries of the Kaapvaal Craton though exceptions are present and new unpublished data suggest that this group may be relatively common on the craton

The IUGS/IAGC Task Group on Global Geochemical Baselines

Science.gov (United States)

Smith, David B.; Wang, Xueqiu; Reeder, Shaun; Demetriades, Alecos

2012-01-01

The Task Group on Global Geochemical Baselines, operating under the auspices of both the International Union of Geological Sciences (IUGS) and the International Association of Geochemistry (IAGC), has the long-term goal of establishing a global geochemical database to document the concentration and distribution of chemical elements in the Earth’s surface or near-surface environment. The database and accompanying element distribution maps represent a geochemical baseline against which future human-induced or natural changes to the chemistry of the land surface may be recognized and quantified. In order to accomplish this long-term goal, the activities of the Task Group include: (1) developing partnerships with countries conducting broad-scale geochemical mapping studies; (2) providing consultation and training in the form of workshops and short courses; (3) organizing periodic international symposia to foster communication among the geochemical mapping community; (4) developing criteria for certifying those projects whose data are acceptable in a global geochemical database; (5) acting as a repository for data collected by those projects meeting the criteria for standardization; (6) preparing complete metadata for the certified projects; and (7) preparing, ultimately, a global geochemical database. This paper summarizes the history and accomplishments of the Task Group since its first predecessor project was established in 1988.

Toward a better understanding of the complex geochemical processes governing subsurface contaminant transport

International Nuclear Information System (INIS)

Puls, R.W.

1990-01-01

Identification and understanding of the geochemical processes, including ion exchange, precipitation, organic partitioning, chemisorption, aqueous complexation, and colloidal stability and transport, controlling subsurface contamination is essential for making accurate predictions of the fate and transport of these constituents. Current approaches to quantify the effect of these processes primarily involve laboratory techniques, including the use of closed static systems (batch experiments) where small amounts of aquifer solids or minerals are contacted with an aqueous phase containing the components of interest for relatively short durations; and dynamic systems (column experiments) where a larger segment of the aquifer is investigated by analyzing the breakthrough profiles of reactive and non-reactive species. Both approaches are constrained by differences in scale, alteration of media during sample collection and use, and spatial variability. More field reactivity studies are needed to complement established laboratory approaches for the determination of retardation factors and scaling factors, corroboration of batch and column results, and validation of sampling techniques. These studies also serve to accentuate areas of geochemical process research where data deficiencies exist, such as the kinetics of adsorption-desorption, metal-organic-mineral interactions, and colloidal mobility. The advantages and disadvantages of the above approaches are discussed in the context of achieving a more completely integrated approach to geochemical transport experiments, with supportive data presented from selected studies. (Author) (16 refs., 4 figs., 2 tabs.)

Reconnaissance Geochemical Study

African Journals Online (AJOL)

distribution patterns. The geochemical distribution maps of the elements reveal that Cu, Pb, Zn, Co, Sc, Ni, Cr, .... After filtration, the leached solutions were diluted with ultra ...... some other rare earth elements in the study area. The occurrence ...

Uranium tailings sampling manual

International Nuclear Information System (INIS)

Feenstra, S.; Reades, D.W.; Cherry, J.A.; Chambers, D.B.; Case, G.G.; Ibbotson, B.G.

1985-01-01

The purpose of this manual is to describe the requisite sampling procedures for the application of uniform high-quality standards to detailed geotechnical, hydrogeological, geochemical and air quality measurements at Canadian uranium tailings disposal sites. The selection and implementation of applicable sampling procedures for such measurements at uranium tailings disposal sites are complicated by two primary factors. Firstly, the physical and chemical nature of uranium mine tailings and effluent is considerably different from natural soil materials and natural waters. Consequently, many conventional methods for the collection and analysis of natural soils and waters are not directly applicable to tailings. Secondly, there is a wide range in the physical and chemical nature of uranium tailings. The composition of the ore, the milling process, the nature of tailings depositon, and effluent treatment vary considerably and are highly site-specific. Therefore, the definition and implementation of sampling programs for uranium tailings disposal sites require considerable evaluation, and often innovation, to ensure that appropriate sampling and analysis methods are used which provide the flexibility to take into account site-specific considerations. The following chapters describe the objective and scope of a sampling program, preliminary data collection, and the procedures for sampling of tailings solids, surface water and seepage, tailings pore-water, and wind-blown dust and radon

Geochemical analysis of the sealing system. Technical Report to work package 9.1.2. Preliminary safety case of the Gorleben site (VSG)

Energy Technology Data Exchange (ETDEWEB)

Xie, Mingliang; Herbert, Horst-Juergen

2012-02-15

The geochemical reaction simulation of ground water and brines with sealing materials for a proposed repository at the Gorleben site is a task under the framework of the VSG project. The calculations presented in this report are aimed to provide a preliminary evaluation of the geochemical stability of three potential engineering barrier materials foreseen in the shaft sealing system in case of groundwater and brine intrusion. The long-term stability of these materials is a key issue for the sealing function of the shaft seals. This is governed by many factors such as geotechnical, hydraulic and geochemical processes. In order to better understand the potential effect of geochemical processes on the long-term properties of these sealing materials, geochemical simulations of the potential interactions between groundwater and brine and shaft sealing materials were performed.

Coupling of transport and geochemical models

International Nuclear Information System (INIS)

Noy, D.J.

1986-01-01

This report considers mass transport in the far-field of a radioactive waste repository, and detailed geochemical modelling of the ground-water in the near-field. A parallel approach to this problem of coupling transport and geochemical codes is the subject of another CEC report (ref. EUR 10226). Both studies were carried out in the framework of the CEC project MIRAGE. (Migration of radionuclides in the geosphere)

k0-NAA implementation and application at IPEN neutron activation laboratory by using the k0-IAEA software: application to geological sample analysis

International Nuclear Information System (INIS)

Mariano, Davi Brigatto

2011-01-01

The Neutron Activation Analysis Laboratory (LAN-IPEN) has been analysing geological samples such as rocks, soils and sediments, for many years with the INAA comparative method, for geochemical and environmental research. This study presents the results obtained in the implementation of the k 0 -standardization method at LAN - IPEN, for geological sample analysis, by using the program k 0 - IAEA, provided by the International Atomic Energy Agency (IAEA). The thermal to epithermal flux ratio f and the shape factor α of the epithermal flux distribution of the IPEN IEA-R1 nuclear reactor were determined for the pneumatic irradiation facility and one selected irradiation position, for short and long irradiations, respectively. To obtain these factors, the 'are triple-monitor' method with 197 Au- 96 Zr- 94 Zr was used. In order to validate the methodology, the geological reference materials basalts JB-1 (GSJ) and BE-N (IWG-GIT), andesite AGV-1 (USGS), granite GS-N (ANRT), SOIL-7 (IAEA) and sediment Buffalo River Sediment (NIST - BRS-8704), which represent different geological matrices, were analysed. The concentration results obtained agreed with assigned values, with bias less than 10% except for Zn in AGV-1 (11.4%) and Mg in GS-N (13.4%). Three different scores were used to evaluate the results: z-score, zeta-score and Uscore. The z-score showed that the results can be considered satisfactory (z 3) for Mn in BE-N, Mg, Ce and La in GS-N, Mg in JB-1, and Th and Eu in Buffalo River Sediment. The U-score test showed that all results, except Mg in JB-1, were within 95% confidence interval. These results indicate excellent possibilities of using this parametric method at the LAN-IPEN for geological samples analysis in geochemical and environmental studies. (author)

Multivariate analysis of the heterogeneous geochemical processes controlling arsenic enrichment in a shallow groundwater system.

Science.gov (United States)

Huang, Shuangbing; Liu, Changrong; Wang, Yanxin; Zhan, Hongbin

2014-01-01

The effects of various geochemical processes on arsenic enrichment in a high-arsenic aquifer at Jianghan Plain in Central China were investigated using multivariate models developed from combined adaptive neuro-fuzzy inference system (ANFIS) and multiple linear regression (MLR). The results indicated that the optimum variable group for the AFNIS model consisted of bicarbonate, ammonium, phosphorus, iron, manganese, fluorescence index, pH, and siderite saturation. These data suggest that reductive dissolution of iron/manganese oxides, phosphate-competitive adsorption, pH-dependent desorption, and siderite precipitation could integrally affect arsenic concentration. Analysis of the MLR models indicated that reductive dissolution of iron(III) was primarily responsible for arsenic mobilization in groundwaters with low arsenic concentration. By contrast, for groundwaters with high arsenic concentration (i.e., > 170 μg/L), reductive dissolution of iron oxides approached a dynamic equilibrium. The desorption effects from phosphate-competitive adsorption and the increase in pH exhibited arsenic enrichment superior to that caused by iron(III) reductive dissolution as the groundwater chemistry evolved. The inhibition effect of siderite precipitation on arsenic mobilization was expected to exist in groundwater that was highly saturated with siderite. The results suggest an evolutionary dominance of specific geochemical process over other factors controlling arsenic concentration, which presented a heterogeneous distribution in aquifers. Supplemental materials are available for this article. Go to the publisher's online edition of the Journal of Environmental Science and Health, Part A, to view the supplemental file.

Geochemical modelling baseline compositions of groundwater

DEFF Research Database (Denmark)

Postma, Diederik Jan; Kjøller, Claus; Andersen, Martin Søgaard

2008-01-01

and variations in water chemistry that are caused by large scale geochemical processes taking place at the timescale of thousands of years. The most important geochemical processes are ion exchange (Valreas and Aveiro) where freshwater solutes are displacing marine ions from the sediment surface, and carbonate......Reactive transport models, were developed to explore the evolution in groundwater chemistry along the flow path in three aquifers; the Triassic East Midland aquifer (UK), the Miocene aquifer at Valreas (F) and the Cretaceous aquifer near Aveiro (P). All three aquifers contain very old groundwaters...... dissolution (East Midlands, Valreas and Aveiro). Reactive transport models, employing the code PHREEQC, which included these geochemical processes and one-dimensional solute transport were able to duplicate the observed patterns in water quality. These models may provide a quantitative understanding...

Initial geochemical characteristics of fluid fine tailings in an oil sands end pit lake

Energy Technology Data Exchange (ETDEWEB)

Dompierre, Kathryn A. [Department of Civil and Geological Engineering, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5A9 (Canada); Lindsay, Matthew B.J., E-mail: matt.lindsay@usask.ca [Department of Geological Sciences, University of Saskatchewan, Saskatoon, Saskatchewan S7N 5E2 (Canada); Cruz-Hernández, Pablo [Department of Geology, University of Huelva, Campus ‘El Carmen’, E-21071 Huelva (Spain); Halferdahl, Geoffrey M. [Environmental Research and Development, Syncrude Canada Limited, Edmonton, Alberta T6N 1H4 (Canada)

2016-06-15

Geochemical characteristics of fluid fine tailings (FFT) were examined in Base Mine Lake (BML), which is the first full-scale demonstration oil sands end pit lake (EPL) in northern Alberta, Canada. Approximately 186 Mm{sup 3} of FFT was deposited between 1994 and 2012, before BML was established on December 31, 2012. Bulk FFT samples (n = 588) were collected in July and August 2013 at various depths at 15 sampling sites. Temperature, solid content, electrical conductivity (EC), pH, Eh and alkalinity were measured for all samples. Detailed geochemical analyses were performed on a subset of samples (n = 284). Pore-water pH decreased with depth by approximately 0.5 within the upper 10 m of the FFT. Major pore-water constituents included Na (880 ± 96 mg L{sup −1}) and Cl (560 ± 95 mg L{sup −1}); Ca (19 ± 4.1 mg L{sup −1}), Mg (11 ± 2.0 mg L{sup −1}), K (16 ± 2.3 mg L{sup −1}) and NH{sub 3} (9.9 ± 4.7 mg L{sup −1}) were consistently observed. Iron and Mn concentrations were low within FFT pore water, whereas SO{sub 4} concentrations decreased sharply across the FFT–water interface. Geochemical modeling indicated that FeS{sub (s)} precipitation was favoured under SO{sub 4}-reducing conditions. Pore water was also under-saturated with respect to gypsum [CaSO{sub 4}·2H{sub 2}O], and near saturation with respect to calcite [CaCO{sub 3}], dolomite [CaMg(CO{sub 3}){sub 2}] and siderite [FeCO{sub 3}]. X-ray diffraction (XRD) suggested that carbonate-mineral dissolution largely depleted calcite and dolomite. X-ray absorption near edge structure (XANES) spectroscopy revealed the presence of FeS{sub (s)}, pyrite [FeS{sub 2}], and siderite. Carbonate-mineral dissolution and secondary mineral precipitation have likely contributed to FFT dewatering and settlement. However, the long-term importance of these processes within EPLs remains unknown. These results provide a reference for assessing the long-term geochemical evolution of oil sands EPLs, and offer

Modeling Background Radiation in our Environment Using Geochemical Data

Energy Technology Data Exchange (ETDEWEB)

Malchow, Russell L.; Marsac, Kara [University of Nevada, Las Vegas; Burnley, Pamela [University of Nevada, Las Vegas; Hausrath, Elisabeth [Uniiversity of Nevada, Las Vegas; Haber, Daniel [University of Nevada, Las Vegas; Adcock, Christopher [University of Nevada, Las Vegas

2015-02-01

Radiation occurs naturally in bedrock and soil. Gamma rays are released from the decay of the radioactive isotopes K, U, and Th. Gamma rays observed at the surface come from the first 30 cm of rock and soil. The energy of gamma rays is specific to each isotope, allowing identification. For this research, data was collected from national databases, private companies, scientific literature, and field work. Data points were then evaluated for self-consistency. A model was created by converting concentrations of U, K, and Th for each rock and soil unit into a ground exposure rate using the following equation: D=1.32 K+ 0.548 U+ 0.272 Th. The first objective of this research was to compare the original Aerial Measurement System gamma ray survey to results produced by the model. The second objective was to improve the method and learn the constraints of the model. Future work will include sample data analysis from field work with a goal of improving the geochemical model.

Concerning evaluation of eco-geochemical background in remediation strategy

Science.gov (United States)

Korobova, Elena; Romanov, Sergey

2015-04-01

The geochemical concept of biosphere developed by V.I. Vernadsky states the geological role of the living organisms in the course of their active chemical interaction with the inert matter (Vernadsky, 1926, 1960). Basing on this theory it is reasonable to suggest that coevolution of living organisms and their environment led to development of the dynamically stable biogeocenoses precisely adequate to their geochemical environment. Soil cover was treated by V.I. Vernadsky as a balanced bio-inert matter resulting from this interaction. Appearance of human mind and then a civilization led to global expansion of human beings, first able to survive in unfavorable geochemical conditions and then starting chemical transformation of the environment to satisfy the growing demands of mankind in food and energy. The residence in unfavorable environment and local contamination was followed by appearance of endemic diseases of plants, animals and man. Therefore zonal, regional and local chemical composition of the soil cover formed in natural conditions may be used for estimation of the optimum geochemical background, most adequate for the corresponding zonal biogeocenoses and species. Moreover, the natural geochemical background and technogenic fields have unequal spatial structure and this facilitates their identification that may be relatively easy realized in remediation strategy. On the assumption of the foregoing, the adequate methodical approach to remediation of technogenically affected areas should account of the interaction of the existing natural and the newly formed technogenic geochemical fields and include the following steps: 1) the study and mapping of geochemical structure of the natural geochemical background basing on soil maps; 2) the study of contaminants and mapping spatial distribution of technogenic releases; 3) construction of risk maps for the target risk groups with due regard to natural ecological threshold concentration in context of risk degree for

Surface geochemical data evaluation and integration with geophysical observations for hydrocarbon prospecting, Tapti graben, Deccan Syneclise, India

Directory of Open Access Journals (Sweden)

T. Satish Kumar

2014-05-01

Full Text Available The Deccan Syneclise is considered to have significant hydrocarbon potential. However, significant hydrocarbon discoveries, particularly for Mesozoic sequences, have not been established through conventional exploration due to the thick basalt cover over Mesozoic sedimentary rocks. In this study, near-surface geochemical data are used to understand the petroleum system and also investigate type of source for hydrocarbons generation of the study area. Soil samples were collected from favorable areas identified by integrated geophysical studies. The compositional and isotopic signatures of adsorbed gaseous hydrocarbons (methane through butane were used as surface indicators of petroleum micro-seepages. An analysis of 75 near-surface soil-gas samples was carried out for light hydrocarbons (C1–C4 and their carbon isotopes from the western part of Tapti graben, Deccan Syneclise, India. The geochemical results reveal sites or clusters of sites containing anomalously high concentrations of light hydrocarbon gases. High concentrations of adsorbed thermogenic methane (C1 = 518 ppb and ethane plus higher hydrocarbons (ΣC2+ = 977 ppb were observed. Statistical analysis shows that samples from 13% of the samples contain anomalously high concentrations of light hydrocarbons in the soil-gas constituents. This seepage suggests largest magnitude of soil gas anomalies might be generated/source from Mesozoic sedimentary rocks, beneath Deccan Traps. The carbon isotopic composition of methane, ethane and propane ranges are from −22.5‰ to −30.2‰ PDB, −18.0‰ to 27.1‰ PDB and 16.9‰–32.1‰ PDB respectively, which are in thermogenic source. Surface soil sample represents the intersection of a migration conduit from the deep subsurface to the surface connected to sub-trappean Mesozoic sedimentary rocks. Prominent hydrocarbon concentrations were associated with dykes, lineaments and presented on thinner basaltic cover in the study area

Petroleum geochemical responses to reservoir rock properties

Energy Technology Data Exchange (ETDEWEB)

Bennett, B.; Larter, S.R. [Calgary Univ., AB (Canada)

2008-07-01

Reservoir geochemistry is used to study petroleum basin development, petroleum mixing, and alterations. In this study, polar non-hydrocarbons were used as proxies for describing reservoir properties sensitive to fluid-rock interactions. A core flood experiment was conducted on a Carboniferous siltstone core obtained from a site in the United Kingdom. Core samples were then obtained from a typical upper shoreface in a North Sea oilfield. The samples were extracted with a dichloromethane and methanol mixture. Alkylcarbazoles and alkylfluorenones were then isolated from the samples. Compositional changes along the core were also investigated. Polar non hydrocarbons were studied using a wireline gamma ray log. The strongest deflections were observed in the basal coarsening upwards unit. The study demonstrated the correlations between molecular markers, and indicated that molecular parameters can be used to differentiate between clean sand units and adjacent coarsening upward muddy sand sequences. It was concluded that reservoir geochemical parameters can provide an independent response to properties defined by petrophysical methods. 6 refs., 2 figs.

Geochemical patterns in soils of the karst region, Croatia

Science.gov (United States)

Prohic, E.; Hausberger, G.; Davis, J.C.

1997-01-01

Soil samples were collected at 420 locations in a 5-km grid pattern in the Istria and Gorski Kotar areas of Croatia, and on the Croatian islands of Cres, Rab and Krk, in order to relate geochemical variation in the soils to underlying differences in geology, bedrock lithology, soil type, environment and natural versus anthropogenic influences. Specific objectives included assessment of possible agricultural and industrial sources of contamination, especially from airborne effluent emitted by a local power plant. The study also tested the adequacy of a fixed-depth soil sampling procedure developed for meager karstic soils. Although 40 geochemical variables were analyzed, only 15 elements and 5 radionuclides are common to all the sample locations. These elements can be divided into three groups: (1) those of mostly anthropogenic origin -Pb, V, Cu and Cr; (2) those of mixed origin - radionuclides and Zn; and (3) those of mostly geogene origin -Ba, Sr, Ti, Al, Na, Ca, Mg, Fe, Mn, Ni and Co. Variation in Pb shows a strong correlation with the pattern of road traffic in Istria. The distributions of Ca, Na and Mg in the flysch basins of southern Istria and Slovenia are clearly distinguishable from the distributions of these elements in the surrounding carbonate terrains, a consequence of differences in bedrock permeability, type of drainage and pH. The spatial pattern of Cs from the Chernobyl nuclear power plant accident reflects almost exclusively the precipitation in Istria during the days immediately after the explosion. ?? 1997 Elsevier Science B.V.

Geochemical processes controlling water salinization in an irrigated basin in Spain: Identification of natural and anthropogenic influence

Energy Technology Data Exchange (ETDEWEB)

Merchán, D., E-mail: d.merchan@igme.es [Geological Survey of Spain — IGME, C/Manuel Lasala 44 9B, 50006 Zaragoza (Spain); Auqué, L.F.; Acero, P.; Gimeno, M.J. [University of Zaragoza — Department of Earth Sciences (Geochemical Modelling Group), C/Pedro Cerbuna 12, 50009 Zaragoza (Spain); Causapé, J. [Geological Survey of Spain — IGME, C/Manuel Lasala 44 9B, 50006 Zaragoza (Spain)

2015-01-01

Salinization of water bodies represents a significant risk in water systems. The salinization of waters in a small irrigated hydrological basin is studied herein through an integrated hydrogeochemical study including multivariate statistical analyses and geochemical modeling. The study zone has two well differentiated geologic materials: (i) Quaternary sediments of low salinity and high permeability and (ii) Tertiary sediments of high salinity and very low permeability. In this work, soil samples were collected and leaching experiments conducted on them in the laboratory. In addition, water samples were collected from precipitation, irrigation, groundwater, spring and surface waters. The waters show an increase in salinity from precipitation and irrigation water to ground- and, finally, surface water. The enrichment in salinity is related to the dissolution of soluble mineral present mainly in the Tertiary materials. Cation exchange, precipitation of calcite and, probably, incongruent dissolution of dolomite, have been inferred from the hydrochemical data set. Multivariate statistical analysis provided information about the structure of the data, differentiating the group of surface waters from the groundwaters and the salinization from the nitrate pollution processes. The available information was included in geochemical models in which hypothesis of consistency and thermodynamic feasibility were checked. The assessment of the collected information pointed to a natural control on salinization processes in the Lerma Basin with minimal influence of anthropogenic factors. - Highlights: • Salinization in Lerma Basin was controlled by the dissolution of soluble salts. • Water salinization and nitrate pollution were found to be independent processes. • High NO{sub 3}, fresh groundwater evolved to lower NO{sub 3}, higher salinity surface water. • Inverse and direct geochemical modeling confirmed the hypotheses. • Salinization was a natural ongoing process

Shale gas characterization based on geochemical and geophysical analysis: Case study of Brown shale, Pematang formation, Central Sumatra Basin

Science.gov (United States)

Haris, A.; Nastria, N.; Soebandrio, D.; Riyanto, A.

2017-07-01

Geochemical and geophysical analyses of shale gas have been carried out in Brown Shale, Middle Pematang Formation, Central Sumatra Basin. The paper is aimed at delineating the sweet spot distribution of potential shale gas reservoir, which is based on Total Organic Carbon (TOC), Maturity level data, and combined with TOC modeling that refers to Passey and Regression Multi Linear method. We used 4 well data, side wall core and 3D pre-stack seismic data. Our analysis of geochemical properties is based on well log and core data and its distribution are constrained by a framework of 3D seismic data, which is transformed into acoustic impedance. Further, the sweet spot of organic-rich shale is delineated by mapping TOC, which is extracted from inverted acoustic impedance. Our experiment analysis shows that organic materials contained in the formation of Middle Pematang Brown Shale members have TOC range from 0.15 to 2.71 wt.%, which is classified in the quality of poor to very good. In addition, the maturity level of organic material is ranging from 373°C to 432°C, which is indicated by vitrinite reflectance (Ro) of 0.58. In term of kerogen type, this Brown shale formation is categorized as kerogen type of II I III, which has the potential to generate a mixture of gasIoil on the environment.

[Study on the method for the determination of trace boron, molybdenum, silver, tin and lead in geochemical samples by direct current arc full spectrum direct reading atomic emission spectroscopy (DC-Arc-AES)].

Science.gov (United States)

Hao, Zhi-hong; Yao, Jian-zhen; Tang, Rui-ling; Zhang, Xue-mei; Li, Wen-ge; Zhang, Qin

2015-02-01

The method for the determmation of trace boron, molybdenum, silver, tin and lead in geochemical samples by direct current are full spectrum direct reading atomic emission spectroscopy (DC-Arc-AES) was established. Direct current are full spectrum direct reading atomic emission spectrometer with a large area of solid-state detectors has functions of full spectrum direct reading and real-time background correction. The new electrodes and new buffer recipe were proposed in this paper, and have applied for national patent. Suitable analytical line pairs, back ground correcting points of elements and the internal standard method were selected, and Ge was used as internal standard. Multistage currents were selected in the research on current program, and each current set different holding time to ensure that each element has a good signal to noise ratio. Continuous rising current mode selected can effectively eliminate the splash of the sample. Argon as shielding gas can eliminate CN band generating and reduce spectral background, also plays a role in stabilizing the are, and argon flow 3.5 L x min(-1) was selected. Evaporation curve of each element was made, and it was concluded that the evaporation behavior of each element is consistent, and combined with the effects of different spectrographic times on the intensity and background, the spectrographic time of 35s was selected. In this paper, national standards substances were selected as a standard series, and the standard series includes different nature and different content of standard substances which meet the determination of trace boron, molybdenum, silver, tin and lead in geochemical samples. In the optimum experimental conditions, the detection limits for B, Mo, Ag, Sn and Pb are 1.1, 0.09, 0.01, 0.41, and 0.56 microg x g(-1) respectively, and the precisions (RSD, n=12) for B, Mo, Ag, Sn and Pb are 4.57%-7.63%, 5.14%-7.75%, 5.48%-12.30%, 3.97%-10.46%, and 4.26%-9.21% respectively. The analytical accuracy was

Geochemical Characterization of Copper Tailings after Legume Revegetation

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Justine Perry T. Domingo

2014-12-01

Full Text Available Knowledge on the geochemistry of mine tailings is important in understanding the challenges in establishing vegetation cover on tailings dumps and mined out areas. In this study, the mineralogy and trace element composition of copper tailings were examined. Two legume species, Calopogonium mucunoides and Centrosema molle, were utilized to investigate the possible effects of these plants in the geochemical development of mine tailings into soil-like material. The initial mineralogical and chemical analysis of the tailings samples indicated poor conditions for plant growth—minimal levels of major nutrients and organic matter as well as elevated copper concentrations. Despite these conditions, the two legume species exhibited good growth rates. Both legumes have likewise signif icantly reduced heavy metal concentrations in the tailings, indicating the possibility of metal hyperaccumulation in the plant tissue. The mineral composition has been retained even after revegetation; nevertheless, breakdown of primary minerals and subsequent formation of clay minerals were detected. These results provide insights on the transformation of toxic materials into habitable substrates for sustained plant growth.

Geochemical prospecting for rare earth elements using termite mound materials

Science.gov (United States)

Horiuchi, Yu; Ohno, Tetsuji; Hoshino, Mihoko; Shin, Ki-Cheol; Murakami, Hiroyasu; Tsunematsu, Maiko; Watanabe, Yasushi

2014-12-01

The Blockspruit fluorite prospect, located in North West State of the Republic of South Africa, occurs within an actinolite rock zone that was emplaced into the Kenkelbos-type granite of Proterozoic age. There are a large number of termite mounds in the prospect. For geochemical prospecting for rare earth elements (REEs), in total, 200 samples of termite mound material were collected from actinolite rock and granite zones in the prospect. Geochemical analyses of these termite mound materials were conducted by two methods: portable X-ray fluorescence (XRF) spectrometry and inductively coupled plasma-mass spectrometry (ICP-MS). Comparison of the two methods broadly indicates positive correlations of REEs (La, Ce, Pr, Nd, and Y), in particular Y and La having a strong correlation. As the result of modal abundance analyses, the actinolite rock at surface mainly consists of ferro-actinolite (89.89 wt%) and includes xenotime (0.26 wt%) and monazite (0.21 wt%) grains as REE minerals. Termite mound materials from actinolite rock also contain xenotime (0.27 wt%) and monazite (0.41 wt%) grains. In addition, termite mound materials from the actinolite rock zone have high hematite and Fe silicate contents compared to those from granite zone. These relationships suggest that REE minerals in termite mound materials originate form actinolite rock. Geochemical anomaly maps of Y, La, and Fe concentrations drawn based on the result of the portable XRF analyses show that high concentrations of these elements trend from SW to NE which broadly correspond to occurrences of actinolite body. These results indicate that termite mounds are an effective tool for REE geochemical prospection in the study area for both light REEs and Y, but a more detailed survey is required to establish the distribution of the actinolite rock body.

Development and Antarctic Testing of a Maneuverable Probe for Clean In-Situ Analysis and Sampling of Subsurface Ice and Subglacial Aquatic Ecosystems

Science.gov (United States)

Francke, G.; Dachwald, B.; Kowalski, J.; Digel, I.; Tulaczyk, S. M.; Mikucki, J.; Feldmann, M.; Espe, C.; Schöngarth, S.; Hiecker, S.; Blandfort, D.; Schüller, K.; Plescher, E.

2016-12-01

There is significant interest in sampling subglacial environments for geochemical and microbiological studies, but those environments are difficult to access. Such environments exist not only on Earth but are also expected beneath the icy crusts of some outer solar system bodies, like the Jovian moon Europa and the Saturnian moon Enceladus. Existing ice drilling technologies make it cumbersome to maintain microbiologically clean access for sample acquisition and environmental stewardship of potentially fragile subglacial aquatic ecosystems. The "IceMole" is a maneuverable subsurface ice probe for clean in-situ analysis and sampling of glacial ice and subglacial materials. The design is based on combining melting and mechanical propulsion, using an ice screw at the tip of the melting head to maintain firm contact between the melting head and the ice. It can change melting direction by differential heating of the melting head and optional side wall heaters. The first two prototypes were successfully tested between 2010 and 2012 on glaciers in Switzerland and Iceland, where they demonstrated downward, horizontal and upward melting, as well as curve driving and dirt layer penetration. Hence, the IceMole allows maneuvers which may be necessary for obstacle avoidance or target selection. Maneuverability, however, necessitates a sophisticated on-board navigation system capable of autonomous operations. Therefore, between 2012 and 2014, a more advanced probe was developed as part of the "Enceladus Explorer" (EnEx) project. The EnEx-IceMole offers systems for relative positioning based on in-ice attitude determination, acoustic positioning, ultrasonic obstacle and target detection, which is all integrated through a high-level sensor fusion. In December 2014, it was used for clean access into a unique subglacial aquatic environment at Blood Falls, Antarctica, where a subglacial brine sample was successfully obtained after about 17 meters of oblique melting. Particular

A Geochemical Mass-Balance Method for Base-Flow Separation, Upper Hillsborough River Watershed, West-Central Florida, 2003-2005 and 2009

Science.gov (United States)

Kish, G.R.; Stringer, C.E.; Stewart, M.T.; Rains, M.C.; Torres, A.E.

2010-01-01

represented somewhat diluted groundwater. Streamflow conductivity integrates the concentrations of the major ions, and the logistics of acquiring specific conductance at frequent time intervals are less complicated than data collection, sample processing, shipment, and analysis of water samples in a laboratory. The acquisition of continuous specific conductance data reduces uncertainty associated with less-frequently collected geochemical point data.

Neutron activation analysis of Permian-Triassic boundary layer samples at the Selong Site in China

International Nuclear Information System (INIS)

Miyamoto, Y.; Sakamoto, K.; Mingqing, W.

1997-01-01

Thirty samples from a limestone stratum across the Permian-Triassic (P-Tr) boundary layer in China were analyzed for 30 elements by instrumental neutron activation analysis, wavelength dispersive X-ray fluorescence and ICP-MS, and also for mineral compositions with a powder X-ray diffractometer. The depth profile was found to indicate a sudden change of elemental and mineral compositions across the P-Tr boundary. Also the profile showed several peaks in elemental concentrations in the lower Permian layered samples as well as in the overlying Triassic strata, which are associated with the change of mineral compositions. Elemental profiles were found to be classified into 4 groups and to give some insights in the geochemical records. Ir is far less abundant (0.1 ppt) compared with that of the K-T boundaries (10 ppb), and the Ir/Co ratio is outside the K-T and Cl chondrite trends. This change of elementary profile is suggestive of the internal causes rather than the external ones such as an asteroid impact for the mass extinction at the P-Tr boundary. (author)

Large Sample Neutron Activation Analysis of Heterogeneous Samples

International Nuclear Information System (INIS)

Stamatelatos, I.E.; Vasilopoulou, T.; Tzika, F.

2018-01-01

A Large Sample Neutron Activation Analysis (LSNAA) technique was developed for non-destructive analysis of heterogeneous bulk samples. The technique incorporated collimated scanning and combining experimental measurements and Monte Carlo simulations for the identification of inhomogeneities in large volume samples and the correction of their effect on the interpretation of gamma-spectrometry data. Corrections were applied for the effect of neutron self-shielding, gamma-ray attenuation, geometrical factor and heterogeneous activity distribution within the sample. A benchmark experiment was performed to investigate the effect of heterogeneity on the accuracy of LSNAA. Moreover, a ceramic vase was analyzed as a whole demonstrating the feasibility of the technique. The LSNAA results were compared against results obtained by INAA and a satisfactory agreement between the two methods was observed. This study showed that LSNAA is a technique capable to perform accurate non-destructive, multi-elemental compositional analysis of heterogeneous objects. It also revealed the great potential of the technique for the analysis of precious objects and artefacts that need to be preserved intact and cannot be damaged for sampling purposes. (author)

Field-based tests of geochemical modeling codes usign New Zealand hydrothermal systems

International Nuclear Information System (INIS)

Bruton, C.J.; Glassley, W.E.; Bourcier, W.L.

1994-06-01

Hydrothermal systems in the Taupo Volcanic Zone, North Island, New Zealand are being used as field-based modeling exercises for the EQ3/6 geochemical modeling code package. Comparisons of the observed state and evolution of the hydrothermal systems with predictions of fluid-solid equilibria made using geochemical modeling codes will determine how the codes can be used to predict the chemical and mineralogical response of the environment to nuclear waste emplacement. Field-based exercises allow us to test the models on time scales unattainable in the laboratory. Preliminary predictions of mineral assemblages in equilibrium with fluids sampled from wells in the Wairakei and Kawerau geothermal field suggest that affinity-temperature diagrams must be used in conjunction with EQ6 to minimize the effect of uncertainties in thermodynamic and kinetic data on code predictions

Use of multiple attributes decision-making Technique for Order Preference by Similarity to Ideal Solution (TOPSIS for Ghare-Gheshlagh calcite in determination of optimum geochemical sampling sites

Directory of Open Access Journals (Sweden)

Mansour Rezaei Azizi

2015-04-01

Full Text Available Introduction Several valuable calcite deposits are located in Ghare-Gheshlagh, south basin of Urmia Lake, NW Iran. Ghare-Gheshlagh area is situated in the northern part of tectono-sedimentary unit, forming NW part of Tertiary Sanandaj-Sirjan geological belt (Stocklin and Nabavi, 1972. The predominant rock types of the area include light color limestones (Qom Formation and Quaternary alluviums and underlined dolomite in depth (Eftekharnejhad, 1973. The thickness of these units varies between 10 cm and 6 meters and up to some hundred meters in length. In the present study, the effect of geochemical parameters responsible for precipitating calcite from the carbonate aqueous fluids is interpreted by the TOPSIS method to find the most preferable sampling sites and geochemical data. Materials and Methods A total of 20 samples were taken from a NE-SW trending profile including 15 calcites of fresh surface outcrops (5 samples per each colored calcite units in order to determine the nature of the rocks. The mineral assemblages were analyzed by optical methods in combination with XRD powder diffraction analysis. Major elements were determined by X-Ray Fluorescence Spectrometry (XRF, trace and rare earth elements were determined by Inductively Coupled Plasma Mass Spectrometry (ICP-MS in Geological Survey of Iran. Results The abundances of trace elements were normalized to the continental crust values (Taylor and McLennan, 1981. The green calcite revealed enrichment in Rb and Sr, while green and white calcite were enriched in U. The U enrichment in the green calcite indicates the reduction condition of deposition. Incompatible elements such as Ba, Th, Nb and P depleted in all calcites. Varying the Sr/Ba value between 3.18 and 5.21% indicates the continental deposition environment and non-magmatic waters as well (Cheng et al., 2013. The Sr2+ content of calcites varies from 123 to 427 ppm, indicates suitable condition for calcite precipitation. Eu anomalies

Overview of the geochemical code MINTEQ: applications to performance assessment for low-level wastes

International Nuclear Information System (INIS)

Graham, M.J.; Peterson, S.R.

1985-09-01

The MINTEQ geochemical computer code, developed at Pacific Northwest Laboratory, integrates many of the capabilities of its two immediate predecessors, WATEQ3 and MINEQL. MINTEQ can be used to perform the calculations necessary to simulate (model) the contact of low-level waste solutions with heterogeneous sediments or the interaction of ground water with solidified low-level wastes. The code is capable of performing calculations of ion speciation/solubility, adsorption, oxidation-reduction, gas phase equilibria, and precipitation/dissolution of solid phases. Under the Special Waste Form Lysimeters-Arid program, the composition of effluents (leachates) from column and batch experiments, using laboratory-scale waste forms, will be used to develop a geochemical model of the interaction of ground water with commercial solidified low-level wastes. The wastes being evaluated include power reactor waste streams that have been solidified in cement, vinyl ester-styrene, and bitumen. The thermodynamic database for the code is being upgraded before the geochemical modeling is performed. Thermodynamic data for cobalt, antimony, cerium, and cesium solid phases and aqueous species are being added to the database. The need to add these data was identified from the characterization of the waste streams. The geochemical model developed from the laboratory data will then be applied to predict the release from a field-lysimeter facility that contains full-scale waste samples. The contaminant concentrations migrating from the wastes predicted using MINTEQ will be compared to the long-term lysimeter data. This comparison will constitute a partical field validation of the geochemical model. 28 refs

X-ray fluorescence analysis with micro glass beads using milligram-scale siliceous samples for archeology and geochemistry

Energy Technology Data Exchange (ETDEWEB)

Ichikawa, Shintaro, E-mail: sichi@meiji.ac.jp [Organization for the Strategic Coordination of Research and Intellectual Properties, Meiji University, Kawasaki 214-8571 (Japan); Nakamura, Toshihiro [Department of Applied Chemistry, Meiji University, Kawasaki 214-8571 (Japan)

2014-06-01

A micro glass bead technique was developed to assay precious siliceous samples for geochemical and archeological analyses. The micro-sized (approximately 3.5 mm in diameter and 0.8 mm in height) glass beads were prepared by mixing and fusing 1.1 mg of the powdered sample and 11.0 mg of the alkali lithium tetraborate flux for wavelength-dispersive X-ray fluorescence determination of major oxides (Na{sub 2}O, MgO, Al{sub 2}O{sub 3}, SiO{sub 2}, P{sub 2}O{sub 5}, K{sub 2}O, CaO, TiO{sub 2}, MnO, and total Fe{sub 2}O{sub 3}). The preparation parameters, including temperature and agitation during the fusing process, were optimized for the use of a commercial platinum crucible rather than a custom-made crucible. The procedure allows preparation of minute sample amounts of siliceous samples using conventional fusing equipment. Synthetic calibration standards were prepared by compounding chemical reagents such as oxides, carbonates, and diphosphates. Calibration curves showed good linearity with r values > 0.997, and the lower limits of detection were in the 10s to 100s of μg g{sup −1} range (e.g., 140 μg g{sup −1} for Na{sub 2}O, 31 μg g{sup −1} for Al{sub 2}O{sub 3}, and 8.9 μg g{sup −1} for MnO). Using the present method, we determined ten major oxides in igneous rocks, stream sediments, ancient potteries, and obsidian. This was applicable to siliceous samples with various compositions, because of the excellent agreement between the analytical and recommended values of six geochemical references. This minimal-scale analysis may be available for precious and limited siliceous samples (e.g., rock, sand, soil, sediment, clay, and archeological ceramics) in many fields such as archeology and geochemistry. - Highlights: • X-ray fluorescence determination of major oxides was performed using 1.1 mg of sample. • Preparation and measurement techniques of the XRF micro glass bead specimen were optimized. • Calibration curves using synthetic standards showed good

Geochemical processes controlling water salinization in an irrigated basin in Spain: identification of natural and anthropogenic influence.

Science.gov (United States)

Merchán, D; Auqué, L F; Acero, P; Gimeno, M J; Causapé, J

2015-01-01

Salinization of water bodies represents a significant risk in water systems. The salinization of waters in a small irrigated hydrological basin is studied herein through an integrated hydrogeochemical study including multivariate statistical analyses and geochemical modeling. The study zone has two well differentiated geologic materials: (i) Quaternary sediments of low salinity and high permeability and (ii) Tertiary sediments of high salinity and very low permeability. In this work, soil samples were collected and leaching experiments conducted on them in the laboratory. In addition, water samples were collected from precipitation, irrigation, groundwater, spring and surface waters. The waters show an increase in salinity from precipitation and irrigation water to ground- and, finally, surface water. The enrichment in salinity is related to the dissolution of soluble mineral present mainly in the Tertiary materials. Cation exchange, precipitation of calcite and, probably, incongruent dissolution of dolomite, have been inferred from the hydrochemical data set. Multivariate statistical analysis provided information about the structure of the data, differentiating the group of surface waters from the groundwaters and the salinization from the nitrate pollution processes. The available information was included in geochemical models in which hypothesis of consistency and thermodynamic feasibility were checked. The assessment of the collected information pointed to a natural control on salinization processes in the Lerma Basin with minimal influence of anthropogenic factors. Copyright © 2014 Elsevier B.V. All rights reserved.

PIXE analysis of thin samples

International Nuclear Information System (INIS)

Kiss, Ildiko; Koltay, Ede; Szabo, Gyula; Laszlo, S.; Meszaros, A.

1985-01-01

Particle-induced X-ray emission (PIXE) multielemental analysis of thin film samples are reported. Calibration methods of K and L X-lines are discussed. Application of PIXE analysis to aerosol monitoring, multielement aerosol analysis is described. Results of PIXE analysis of samples from two locations in Hungary are compared with the results of aerosol samples from Scandinavia and the USA. (D.Gy.)

Groundwater sampling in uranium reconnaissance

International Nuclear Information System (INIS)

Butz, T.R.

1977-03-01

The groundwater sampling program is based on the premise that ground water geochemistry reflects the chemical composition of, and geochemical processes active in the strata from which the sample is obtained. Pilot surveys have shown that wells are the best source of groundwater, although springs are sampled on occasion. The procedures followed in selecting a sampling site, the sampling itself, and the field measurements, as well as the site records made, are described

Evaluation of processes controlling the geochemical constituents in deep groundwater in Bangladesh: Spatial variability on arsenic and boron enrichment

International Nuclear Information System (INIS)

Halim, M.A.; Majumder, R.K.; Nessa, S.A.; Hiroshiro, Y.; Sasaki, K.; Saha, B.B.; Saepuloh, A.; Jinno, K.

2010-01-01

Forty-six deep groundwater samples from highly arsenic affected areas in Bangladesh were analyzed in order to evaluate the processes controlling geochemical constituents in the deep aquifer system. Spatial trends of solutes, geochemical modeling and principal component analysis indicate that carbonate dissolution, silicate weathering and ion exchange control the major-ion chemistry. The groundwater is dominantly of Na-Cl type brackish water. Approximately 17% of the examined groundwaters exhibit As concentrations higher than the maximum acceptable limit of 10 μg/L for drinking water. Strong correlation (R 2 = 0.67) of Fe with dissolved organic carbon (DOC) and positive saturation index of siderite suggests that the reductive dissolution of Fe-oxyhydroxide in presence of organic matter is considered to be the dominant process to release high content of Fe (median 0.31 mg/L) in the deep aquifer. In contrast, As is not correlated with Fe and DOC. Boron concentration in the 26% samples exceeds the standard limit of 500 μg/L, for water intended for human consumption. Negative relationships of B/Cl ratio with Cl and boron with Na/Ca ratio demonstrate the boron in deep groundwater is accompanied by brackish water and cation exchange within the clayey sediments.

Geochemical Survey of Pernambuco

International Nuclear Information System (INIS)

Horowitz, A.; Duarte, P.J.; Almeida, M.G. de; Medeiros, M.O.

1988-01-01

The area studied i this work is located in a triangle formed by the Sibiro and Boca da Mata Sugar-Mills and Serinhaem country. In the Cabo Formation the search determinated conglomerates, arcos and clays. Although the highest geochemical activity have been done in the decomposed crystalin, and the values from Cabo Formation don't be encourager, this formation has lithology compatible with uranium mineralization. The Cabo Formation's sediments presents lithologic variations very expressives, with conglomerates, arcoses and clay silts, which determinate the choise of the area. This area presented favorable to uranium prospecting and to others elements interesting to ragional geochemistry. The atomic absorption analysis, fluorimetry and spectrometry were done for the following elements: Zn, V, Ti, Ni, Pb, Mn, Ga, Cu, Co, Bi, Ag, B, Mo, and U. (C.D.G.) [pt

Sampling and sample processing in pesticide residue analysis.

Science.gov (United States)

Lehotay, Steven J; Cook, Jo Marie

2015-05-13

Proper sampling and sample processing in pesticide residue analysis of food and soil have always been essential to obtain accurate results, but the subject is becoming a greater concern as approximately 100 mg test portions are being analyzed with automated high-throughput analytical methods by agrochemical industry and contract laboratories. As global food trade and the importance of monitoring increase, the food industry and regulatory laboratories are also considering miniaturized high-throughput methods. In conjunction with a summary of the symposium "Residues in Food and Feed - Going from Macro to Micro: The Future of Sample Processing in Residue Analytical Methods" held at the 13th IUPAC International Congress of Pesticide Chemistry, this is an opportune time to review sampling theory and sample processing for pesticide residue analysis. If collected samples and test portions do not adequately represent the actual lot from which they came and provide meaningful results, then all costs, time, and efforts involved in implementing programs using sophisticated analytical instruments and techniques are wasted and can actually yield misleading results. This paper is designed to briefly review the often-neglected but crucial topic of sample collection and processing and put the issue into perspective for the future of pesticide residue analysis. It also emphasizes that analysts should demonstrate the validity of their sample processing approaches for the analytes/matrices of interest and encourages further studies on sampling and sample mass reduction to produce a test portion.

Applications of prospecting geochemical techniques to the search for and to the study of uranium deposits in metropolitan France; Applications des techniques geochimiques de prospection a la recherche et a l'etude des gites uraniferes en France metropolitaine

Energy Technology Data Exchange (ETDEWEB)

Grimbert, Arnold

1957-07-01

After having recalled facts which leaded the CEA to use new geochemical techniques for the prospecting of uranium deposits through sampling and analysis of soils and waters, the author describes the organisation and methods implemented for this prospecting activity: team composition for sampling and analysis, role of each engineer and technician in the prospecting stages (preliminary study, routine prospecting, result interpretation), sampling and analysis processes. He also reports campaigns of geochemical prospecting: study of the La Chapelle Largeau deposit (objectives, geological context, preliminary study, routine prospecting, study of geochemical anomalies), tactical research on Verneix indices (study of radioactivity anomaly discovered by radio-prospecting), strategical searches in a non prospected area in the South of Avallon. The author discusses the issues of efficiency and cost price of this geochemical prospecting technique in soils and in waters. Appendices present the equipment and operation modality for soil sampling, and for soil sample preparation, and principles, equipment and products for soil analysis and for water analysis [French] A la suite des resultats satisfaisants obtenus dans la recherche de methodes de dosage adaptees au cas de l'uranium, la Direction des Recherches Minieres du Commissariat a l'Energie atomique a decide, en decembre 1954, d'utiliser, conjointement avec les methodes classiques de prospection, les techniques geochimiques pour la recherche et l'etude des gites uraniferes. Ces applications pratiques ont ete confiees a une Section de Geochimie dont l'organisation, les moyens en personnel et en materiel, ainsi que les methodes de travail, font l'objet d'un expose detaille. Quelques exemples de prospection, en France metropolitaine, montrent la nature des problemes poses (etude d'un gisement connu, recherche tactique sur des indices, recherche strategique dans une region non prospectee), les methodes utilisees pour les

Geochemical evolution of groundwater in carbonate aquifers of southern Latium region, central Italy

Directory of Open Access Journals (Sweden)

Giuseppe Sappa

2013-03-01

Full Text Available Spring and well water samples, from carbonate aquifers of Latium region, have been characterized to determine the hydrochemical processes governing the evolution of the groundwater. Most of the spring samples, issuing from Lepini, Ausoni and Aurunci Mts., are characterized as alkaline earth HCO3 waters, however, some samples show a composition of Cl--SO4 -- alkaline earth waters. Groundwater samples from Pontina Plain shows three different hydrochemical facies: alkaline earth HCO3 type, Cl-- SO4 -- alkaline earth type and Cl--SO4 -- alkaline type waters. Geochemical modeling and saturation index computation of the sampled waters show an interaction with calcareous and calcareous-dolomitic lithologies. Most of the springs and wells was kinetically saturated with respect to calcite and dolomite, and all the samples were below the equilibrium state with gypsum. This indicates that the groundwater has capacity to dissolve the gypsum along the flow paths. The electrical conductivity and Cl- concentrations of the sampled waters show a positive trend with the decrease in the distance from the coast, highlighting seawater intrusion in the coastal area. According to hydrochemistry results and geochemical modeling, the dominant factors in controlling the hydrochemical characteristics of groundwater are: (i water rock interaction with calcareous and calcareous-dolomitic lithologies; (ii seawater intrusion in the coastal area; (iii dissolution and/or precipitation of carbonate and (i.e. dolomite and calcite evaporate minerals (gypsum determined by saturation indexes; (iv mineral weathering process; (the high Mg/Ca ratio due to the weathering of Mg-rich dolomite.

Monitoring active volcanoes: The geochemical approach

Directory of Open Access Journals (Sweden)

Takeshi Ohba

2011-06-01

Full Text Available

The geochemical surveillance of an active volcano aims to recognize possible signals that are related to changes in volcanic activity. Indeed, as a consequence of the magma rising inside the volcanic "plumbing system" and/or the refilling with new batches of magma, the dissolved volatiles in the magma are progressively released as a function of their relative solubilities. When approaching the surface, these fluids that are discharged during magma degassing can interact with shallow aquifers and/or can be released along the main volcano-tectonic structures. Under these conditions, the following main degassing processes represent strategic sites to be monitored.

The main purpose of this special volume is to collect papers that cover a wide range of topics in volcanic fluid geochemistry, which include geochemical characterization and geochemical monitoring of active volcanoes using different techniques and at different sites. Moreover, part of this volume has been dedicated to the new geochemistry tools.

Geochemical mapping of the Hyeonri, Bongpyeong, Yeongog and Doam sheets (1:50,000)

Energy Technology Data Exchange (ETDEWEB)

Lee, Jin Soo; Seo, Hyo Joon [Korea Institute of Geology Mining and Materials, Taejon (Korea, Republic of)

1997-12-01

A geochemical mapping was made on the four quadrangles of the Hyeonri, Bongpyeong, Yeongog and Doam Sheets (1:50,000) located in the northeastern part of South Korea. The area of about 2,500 Km{sup 2} is covered mostly the Precambrian metamorphic rocks and Jurassic granites, and partly by Permo-Triassic sedimentary and Cretaceous granites. Geochemical samples of stream sediment and natural surface water, totally 713 for each media, were systematically collected from in the primary and secondary order streams. The samples were chemically analysed for the trace elements by ICP, and anion elements of water samples were determined by IC. The pH. EC (electrical conductivity) Eh, DO (dissolved oxygen) and bicarbonate were measured in situ by digital portable equipment. Several deposits of gold, fluorite, molybdenite and iron deposits were weakly formed at or around the contact zone between metamorphic rocks and granites. The coal mines were actively operated until 1970`s in the southeastern part of the area. At present, none of them is operating owing to shortage of ore reserves and higher mining cost excepting a few non-metallic or construction stone mines. Geochemical anomalies were revealed out several areas deriving from mineralized factors or effected by some polluted evidences of human life. The anomalies of Pb, Zn, Co, Cr, Cd, etc for sulfide minerals were poorly confined around old prospects or calcareous formation of Chosun Supergroup. The conductivity of stream in the Odae national park is extremely high value to be expecting mineral deposit such as uranium or rare earth metals etc.. The anomalies with Cl, Na, Mg, NO{sub 3}, HCO{sub 3} near or along the expressway and main roads where the population, are densely, were identified to be polluted by human activities and stock-farming. (author). 36 refs., 11 tabs., 57 figs.

Coupling between a geochemical model and a transport model of dissolved elements

International Nuclear Information System (INIS)

Jacquier, P.

1988-10-01

In order to assess the safety analysis of an underground repository, the transport of radioelements in groundwater and their interactions with the geological medium are modelled. The objective of this work is the setting up and experimental validation of the coupling of a geochemical model with a transport model of dissolved elements. A laboratory experiment was developed at the CEA center of Cadarache. Flow-through experiments were carried out on columns filled with crushed limestone, where several inflow conditions were taken into account as the temperature, the presence of a pollutant (strontium chloride) at different concentrations. The results consist of the evolution of the chemical composition of the water at the outlet of the column. The final aim of the study is to explain these results with a coupled model where geochemical and transport phenomena are modelled in a two-step procedure. This code, called STELE, was built by introducing a geochemical code, CHIMERE, into an existing transport code, METIS. At this stage, the code CHIMERE can take into account: any chemical reaction in aqueous phase (complexation, acid-base reaction, redox equilibrium), dissolution-precipitation of minerals and solid phases, dissolution-degassing of gas. The paper intends to describe the whole process leading to the coupling which can be forecasted over the next years between geochemical and transport models

Alligator Rivers Analogue project. Geochemical Data Bases

International Nuclear Information System (INIS)

Bennett, D.G.; Read, D.

1992-01-01

The Koongarra uranium deposit in the Northern Territory of Australia is being studied to evaluate the processes involved in the geochemical alteration of the ore body and the formation of the uranium dispersion fan. A broad range of research is being undertaken into the geochemistry and hydrology of the site with the aim of understanding the transport of radionuclides through the system. During the project a range of geochemical and hydrogeochemical models have been developed to account for measured data from the site and with which to predict site evolution. The majority of these models are based on the premise of thermodynamic chemical equilibrium and employ fundamental thermodynamic data to characterise the chemistry of the system. From the differences which exist between the thermodynamic data bases (Appendices I and II) it is possible to gain a view of the level of uncertainty associated with thermodynamic data in each set of calculations. This report gives a brief introduction to the geochemical processes underlying the models, and details the equations used to quantify the more common of these processes (e.g. aqueous speciation and mineral solubility). A description is given of the computer codes (EQ3/6, PHREEQE, MINTEQ) most commonly used during the project for geochemical modelling. Their key features are highlighted and comparisons made. It is concluded that the degree of uncertainty in geochemical modelling studies arising as a result of using one code rather than another is relatively insignificant when compared to that related to differences in the underlying data bases. 73 refs., 3 figs

Petrological, geochemical and isotopic characteristics of lignite and calcified lignite from mining area Pesje, Velenje Basin, Slovenia

Science.gov (United States)

Vrabec, Mirijam; Markič, Miloš; Vrabec, Marko; Jaćimović, Radojko; Kanduč, Tjaša

2014-05-01

Lignite (organic rich) and calcified lignite (inorganic rich) samples from excavation field -50c mining area Pesje, Velenje Basin, Slovenia were investigated. During geological and structural mapping lignite and calcified lignite samples were systematically taken for determination of their petrological, geochemical and isotopic characteristics. Lignite is composed of fine detritical gelified matrix. At least five different types of calcified lignite were recognized forming laminations, calcifications after wood, petrified wood and complete replacements of lignite with carbonate. All measured parameters so far indicate geochemical processes during sedimentation of the Velenej Basin. After macroscopic description samples were split to organic and inorganic component (Ward, 1984) and powdered in an agate mortar for geochemical and isotopic analyses. Major and trace elements (As, B, Ba, Cd, Co, Cr, Cu, Hg, Mn, Mo, Sb, Se, Th, U, Zn) in these samples were determined by instrumental neutron activation analysis (INAA) using k-0 standardization method (Jaćimović et al, 2002). The isotopic composition of carbon and nitrogen was determined using a Europa 20-20 continuous flow IRMS ANCA-SL preparation module. A 1 mg amount of a sample was weighed in a tin capsule for carbon and 10 mg for nitrogen analysis. Samples for carbon analyses were pretreated with 1 M HCl to remove carbonates. Carbonate samples from carbonate-rich strata and calcified xylite were first roasted at 450 deg C (Krantz et al., 1987). Three miligrams of carbonate sample was transformed into CO2 by reaction with anhydrous H3PO4 at 55 deg C under vacuum (McCrea, 1950) and measured with GV 2003 isotope ratio mass spectrometer. Measured isotopic composition of oxygen as VPDB values was recalculated to the VSMOW reference standard to enable the comparison with data from other coal basins. SEM/EDXS of carbonate rich sediments was performed with JEOL JSM 5800 electron microanalyzer scanning electron microscope

Source areas of the Grybów sub-basin: micropaleontological, mineralogical and geochemical provenance analysis (Outer Western Carpathians, Poland

Directory of Open Access Journals (Sweden)

Oszczypko-Clowes Marta

2015-12-01

Full Text Available The Grybów Unit occurring in the Ropa tectonic window was the subject of micropaleontological and geochemical investigation. Studies, based on calcareous nannofossils, proved that the level of reworked microfossil is not higher than 22 % and it varies between two sections. Quantitative analyses of the reworked assemblages confirmed the domination of Cretaceous and Middle Eocene species. The Sub-Grybów Beds, Grybów Marl Formation and Krosno Beds were assigned to the Late Oligocene and represent the terminal flysch facies. Detrital material accumulated in the Oligocene sediments originated from the Marmarosh Massif, which is the eastern prolongation of the Fore-Magura Ridge. The microscopically obtained petrological features agree with the chemical composition of the samples. Mica flakes, rounded grains of glauconite, heavy mineral assemblage, including abraded grains of zircon, rutile and tourmaline as well as charred pieces of plant tissues are reworked components. Enrichment in zircon and rutile is confirmed geochemically by positive correlation between Zr and SiO2. Zr addition is illustrated on 10×Al2O3–Zr–200×TiO2 and Zr/Sc vs. Th/Sc diagrams. Interpretation of the A–CN–K diagram and variety of CIA and CPA values indicate that the source rocks were intensely weathered granite-type rocks.

The geological, geochemical, topographical and hydrogeological characteristics of the Broubster natural analogue site, Caithness

International Nuclear Information System (INIS)

Ball, T.K.; Milodowski, A.E.

1991-01-01

One of the four analogue sites chosen for investigation by the British Geological Survey is the uranium mineralization at Broubster, Caithness, Scotland. Naturally occurring uranium has been leached from a thin mineralized limestone horizon and has been carried by groundwater flow into a peat bog about 100 m away. This process has probably been going on for at least 5 000 years. Standard surveying, hydrogeological and geochemical methods have been applied in the investigation and analysis of the area. Selected samples of the mineralization, peat soils and associated groundwaters have been examined in detail. This report summarizes the main findings accumulated since 1968 when the site was first discovered, and provides a useful information base for further modelling work. 27 refs.; 12 plates; 40 figs.; 17 tabs

The geological, geochemical, topographical and hydrogeological characteristics of the Broubster natural analogue site, Caithness

International Nuclear Information System (INIS)

Ball, T.K.; Milodowski, A.E.

1989-06-01

One of the four natural analogue sites chosen for investigation by the British Geological Survey is the uranium mineralisation at Broubster, Caithness, Scotland. Naturally occurring uranium has been leached from a thin mineralised limestone horizon and has been carried by groundwater flow into a peat bog about 100m away. This process has probably been going on for at least 5000 years. Standard surveying, hydrogeological and geochemical methods have been applied in the investigation and analysis of the area. Selected samples of the mineralisation, peat soils and associated groundwaters have been examined in detail. This report summarises the main findings accumulated since 1968 when the site was first discovered, and provides a useful information base for further modelling work. (author)

Hydro-geochemical analysis of a degraded dune slack

NARCIS (Netherlands)

Grootjans, AP; Sival, FP; Stuyfzand, PJ

A hydrochemical analysis of the groundwater composition was carried out in a degraded dune slack complex in order to assess the prospects for regeneration of low productivity, basiphilous vegetation types, typical of natural dune slacks. Two hundred and fifty water samples, most of them obtained

An overview of the geochemical code MINTEQ: Applications to performance assessment for low-level wastes

International Nuclear Information System (INIS)

Peterson, S.R.; Opitz, B.E.; Graham, M.J.; Eary, L.E.

1987-03-01

The MINTEQ geochemical computer code, developed at the Pacific Northwest Laboratory (PNL), integrates many of the capabilities of its two immediate predecessors, MINEQL and WATEQ3. The MINTEQ code will be used in the Special Waste Form Lysimeters-Arid program to perform the calculations necessary to simulate (model) the contact of low-level waste solutions with heterogeneous sediments of the interaction of ground water with solidified low-level wastes. The code can calculate ion speciation/solubilitya, adsorption, oxidation-reduction, gas phase equilibria, and precipitation/dissolution of solid phases. Under the Special Waste Form Lysimeters-Arid program, the composition of effluents (leachates) from column and batch experiments, using laboratory-scale waste forms, will be used to develop a geochemical model of the interaction of ground water with commercial, solidified low-level wastes. The wastes being evaluated include power-reactor waste streams that have been solidified in cement, vinyl ester-styrene, and bitumen. The thermodynamic database for the code was upgraded preparatory to performing the geochemical modeling. Thermodynamic data for solid phases and aqueous species containing Sb, Ce, Cs, or Co were added to the MINTEQ database. The need to add these data was identified from the characterization of the waste streams. The geochemical model developed from the laboratory data will then be applied to predict the release from a field-lysimeter facility that contains full-scale waste samples. The contaminant concentrations migrating from the waste forms predicted using MINTEQ will be compared to the long-term lysimeter data. This comparison will constitute a partial field validation of the geochemical model

Geochemical evaluation of Pabdeh Formation in Nosrat field, southeast Persian Gulf using Rock- Eval VI pyrolysis

Directory of Open Access Journals (Sweden)

mohammad sadeghi

2015-02-01

Full Text Available The present study was performed on 59 drillhole cuttings from Pabdeh Formation in Nosrat oil field using Rock- Eval VI pryrolysis. Geochemical analysis indicated that Pabdeh Formation possesses poor to good hydrocarbon potential. Plotting S1 against TOC suggests that samples were not affected by polluting substances such as crude oil and lubricants while drilling operation. Jones organic fancies diagram shows B-BC area indicating that Pabdeh Formation was deposited in marine anoxic to oxic environments. HI vesus Tmax shows that most samples initially have had type II kerogen and now reflecting a mixture of type II to III kerogen (capable of generating oil that have already entered oil generation window. In addition, S1+S2 versus TOC plot also suggests that Pabdeh Formation can be considered as a capable hydrocarbon generating source rock in the study area.

pplication of Fractal Technique for Analysis of Geophysical - Geochemical Databases in Tekieh Pb-Zn Ore Deposit (SE of Arak

Directory of Open Access Journals (Sweden)

Seyed Reza Mehrnia

2017-02-01

should emphasize on self-organized distribution of Pb-Zn anomalies to introduce a new set of nonlinear distributions in order to find the confidence regression coefficients between the variables. As the final results, fractal analysis of available databases represented new target areas with better mineralization aggregations than linear analysis of the anomalous regions according to micrographs. It means that surficial mineralization processes could be extended in depth and enriched next to altered host units because of a nonlinear but self-organized distribution of geochemical- geophysical anomalies in Tekieh ore deposit region. References Annells, R.N., Arthurton, R.S., Bazley, R.A.B., Davies, R.G., Hamedi, M.A.R. and Rahimzadeh, F.R., 1985. Geological Map of Shazand- Khomein. Scale: 1:100000, Cartographic Department of Geological Survey of Iran. Calagari, A.A., 2010. Principles of geophysical explorations. University of Tabriz, Tabriz, 485 pp. Jafari, H., 2007. Using geoelectrical techniques for Zn-Pb explorations in Haft-Emarat district, Tekieh region (South East of Arak. Kimya Kavan Tosee Novin Company, Tehran, 206 pp. Mandelbrot, B., 2005. Fractal Geometry of Nature. W.H Freeman & Company, New York, 468 pp. Mehrnia, S.R.,2013. Application of fractal geometry for recognizing the pattern of textural zoning in epithermal deposits: (case study: Shikhdarabad Au-Cu indices East- Azerbaijan province. Journal of Economic Geology, 5(1: 23-36. (in Persian Momenzadeh, M. and Ziseman, H., 1981. Lead – Zinc re mineralization potentials in Malayer – Esfahan district. Journal of Ore Deposit, 3(1: 88-101. Salehi, L., 2004. Geochemistry of REE content in Tekieh Pb-Zn ore deposit. M.Sc. Thesis, Shahid Beheshti University, Tehran, Iran, 181 pp. Torkashvand, S., Mehrnia, S.R. and Moghaddasi, S.J., 2009. Co-Processing of the geophysical parameters for Tekieh Zn-Pb ore deposits (south east of Arak. 4th PNU Geological National Conference, Payam Noor University of Mashhad, Mashhad

An integrated geophysical and geochemical exploration of critical zone weathering on opposing montane hillslope

Science.gov (United States)

Singha, K.; Navarre-Sitchler, A.; Bandler, A.; Pommer, R. E.; Novitsky, C. G.; Holbrook, S.; Moore, J.

2017-12-01

Quantifying coupled geochemical and hydrological properties and processes that operate in the critical zone is key to predicting rock weathering and subsequent transmission and storage of water in the shallow subsurface. Geophysical data have the potential to elucidate geochemical and hydrologic processes across landscapes over large spatial scales that are difficult to achieve with point measurements alone. Here, we explore the connections between weathering and fracturing, as measured from integrated geochemical and geophysical borehole data and seismic velocities on north- and south-facing aspects within one watershed in the Boulder Creek Critical Zone Observatory. We drilled eight boreholes up to 13 m deep on north- and south-facing aspects within Upper Gordon Gulch, and surface seismic refraction data were collected near these wells to explore depths of regolith and bedrock, as well as anisotropic characteristics of the subsurface material due to fracturing. Optical televiewer data were collected in these wells to infer the dominant direction of fracturing and fracture density in the near surface to corroborate with the seismic data. Geochemical samples were collected from four of these wells and a series of shallow soil pits for bulk chemistry, clay fraction, and exchangeable cation concentrations to identify depths of chemically altered saprolite. Seismic data show that depth to unweathered bedrock, as defined by p-wave seismic velocity, is slightly thicker on the north-facing slopes. Geochemical data suggest that the depth to the base of saprolite ranges from 3-5 m, consistent with a p-wave velocity value of 1200 m/s. Based on magnitude and anisotropy of p-wave velocities together with optical televiewer data, regolith on north-facing slopes is thought to be more fractured than south-facing slopes, while geochemical data indicate that position on the landscape is another important characteristic in determining depths of weathering. We explore the importance

Stream-sediment geochemical prospecting for uranium in the Paleozoic of the Belgian Ardennes

International Nuclear Information System (INIS)

Martin, H.; Lefin, J.P.; Dejonghe, L.; Henry, J.

1983-01-01

Orientation studies showed that a positive geochemical response for uranium in the Belgium Ardennes could be obtained with bank sampling, which consists of collecting colluvium and alluvium on both sides of the rivers. This necessitates a large sampling density of about one sample per km 2 (10 205 samples from an area of 11 000 km 2 ). Anomalies (> 3 ppm) are found that fall into three main areas each in a different geological setting: (1) at the periphery of the Cambro-Silurian Massif of Stavelot; (2) within the transition beds between the Visean and Namurian; and (3) in the lower Devonian of the central Ardennes. (Auth.)

Mineralization and geochemical studies in the Kalchouyeh occurrence, southwest of Naein

OpenAIRE

Hengameh Hosseini Dinani; Hashem Bagheri; Reza Shamsipour Dehkordi

2012-01-01

Kalchouyeh area in southwest of Naein is located in the Urumieh-Dokhtar volcano-plutonic belt. Mineralization occurred mainly as disseminations and veinlets hosted by trachy-andesite and pyroxene andesites. For mineralogy, alteration, fluid inclusion and geochemical studies, the two major mineralized zones: A (larger vein) from the north-northwest and B (smaller vein) from the east-southeast of the area were sampled. Alteration studies revealed that the main alteration assemblages are silicif...

Hydrogeochemical and stream sediment detailed geochemical survey for Edgemont, South Dakota; Wyoming

Energy Technology Data Exchange (ETDEWEB)

Butz, T.R.; Dean, N.E.; Bard, C.S.; Helgerson, R.N.; Grimes, J.G.; Pritz, P.M.

1980-05-31

Results of the Edgemont detailed geochemical survey are reported. Field and laboratory data are presented for 109 groundwater and 419 stream sediment samples. Statistical and areal distributions of uranium and possible uranium-related variables are given. A generalized geologic map of the survey area is provided, and pertinent geologic factors which may be of significance in evaluating the potential for uranium mineralization are briefly discussed. Groundwaters containing greater than or equal to 7.35 ppB uranium are present in scattered clusters throughout the area sampled. Most of these groundwaters are from wells drilled where the Inyan Kara Group is exposed at the surface. The exceptions are a group of samples in the northwestern part of the area sampled and south of the Dewey Terrace. These groundwaters are also produced from the Inyan Kara Group where it is overlain by the Graneros Group and alluvium. The high uranium groundwaters along and to the south of the terrace are characterized by high molybdenum, uranium/specific conductance, and uranium/sulfate values. Many of the groundwaters sampled along the outcrop of the Inyan Kara Group are near uranium mines. Groundwaters have high amounts of uranium and molybdenum. Samples taken downdip are sulfide waters with low values of uranium and high values of arsenic, molybdenum, selenium, and vanadium. Stream sediments containing greater than or equal to 5.50 ppM soluble uranium are concentrated in basins draining the Graneros and Inyan Kara Groups. These values are associated with high values for arsenic, selenium, and vanadium in samples from both groups. Anomalous values for these elements in the Graneros Group may be caused by bentonite beds contained in the rock units. As shown on the geochemical distribution plot, high uranium values that are located in the Inyan Kara Group are almost exclusively draining open-pit uranium mines.

Recent developments and evaluation of selected geochemical techniques applied to uranium exploration

International Nuclear Information System (INIS)

Wenrich-Verbeek, K.J.; Cadigan, R.A.; Felmlee, J.K.; Reimer, G.M.; Spirakis, C.S.

1976-01-01

Various geochemical techniques for uranium exploration are currently under study by the geochemical techniques team of the Branch of Uranium and Thorium Resources, US Geological Survey. Radium-226 and its parent uranium-238 occur in mineral spring water largely independently of the geochemistry of the solutions and thus are potential indicators of uranium in source rocks. Many radioactive springs, hot or cold, are believed to be related to hydrothermal systems which contain uranium at depth. Radium, when present in the water, is co-precipitated in iron and/or manganese oxides and hydroxides or in barium sulphate associated with calcium carbonate spring deposits. Studies of surface water samples have resulted in improved standardized sample treatment and collection procedures. Stream discharge has been shown to have a significant effect on uranium concentration, while conductivity shows promise as a ''pathfinder'' for uranium. Turbid samples behave differently and consequently must be treated with more caution than samples from clear streams. Both water and stream sediments should be sampled concurrently, as anomalous uranium concentrations may occur in only one of these media and would be overlooked if only one, the wrong one, were analysed. The fission-track technique has been applied to uranium determinations in the above water studies. The advantages of the designed sample collecting system are that only a small quantity, typically one drop, of water is required and sample manipulation is minimized, thereby reducing contamination risks. The fission-track analytical technique is effective at the uranium concentration levels commonly found in natural waters (5.0-0.01 μg/litre). Landsat data were used to detect alteration associated with uranium deposits. Altered areas were detected but were not uniquely defined. Nevertheless, computer processing of Landsat data did suggest a smaller size target for further evaluation and thus is useful as an exploration tool

Hydrogeochemical and stream sediment detailed geochemical survey for Edgemont, South Dakota; Wyoming

International Nuclear Information System (INIS)

Butz, T.R.; Dean, N.E.; Bard, C.S.; Helgerson, R.N.; Grimes, J.G.; Pritz, P.M.

1980-01-01

Results of the Edgemont detailed geochemical survey are reported. Field and laboratory data are presented for 109 groundwater and 419 stream sediment samples. Statistical and areal distributions of uranium and possible uranium-related variables are given. A generalized geologic map of the survey area is provided, and pertinent geologic factors which may be of significance in evaluating the potential for uranium mineralization are briefly discussed. Groundwaters containing greater than or equal to 7.35 ppB uranium are present in scattered clusters throughout the area sampled. Most of these groundwaters are from wells drilled where the Inyan Kara Group is exposed at the surface. The exceptions are a group of samples in the northwestern part of the area sampled and south of the Dewey Terrace. These groundwaters are also produced from the Inyan Kara Group where it is overlain by the Graneros Group and alluvium. The high uranium groundwaters along and to the south of the terrace are characterized by high molybdenum, uranium/specific conductance, and uranium/sulfate values. Many of the groundwaters sampled along the outcrop of the Inyan Kara Group are near uranium mines. Groundwaters have high amounts of uranium and molybdenum. Samples taken downdip are sulfide waters with low values of uranium and high values of arsenic, molybdenum, selenium, and vanadium. Stream sediments containing greater than or equal to 5.50 ppM soluble uranium are concentrated in basins draining the Graneros and Inyan Kara Groups. These values are associated with high values for arsenic, selenium, and vanadium in samples from both groups. Anomalous values for these elements in the Graneros Group may be caused by bentonite beds contained in the rock units. As shown on the geochemical distribution plot, high uranium values that are located in the Inyan Kara Group are almost exclusively draining open-pit uranium mines

Examining Volcanic Terrains Using In Situ Geochemical Technologies; Implications for Planetary Field Geology

Science.gov (United States)

Young, K. E.; Bleacher, J. E.; Evans, C. A.; Rogers, A. D.; Ito, G.; Arzoumanian, Z.; Gendreau, K.

2015-01-01

Regardless of the target destination for the next manned planetary mission, the crew will require technology with which to select samples for return to Earth. The six Apollo lunar surface missions crews had only the tools to enable them to physically pick samples up off the surface or from a boulder and store those samples for return to the Lunar Module and eventually to Earth. Sample characterization was dependent upon visual inspection and relied upon their extensive geology training. In the four decades since Apollo however, great advances have been made in traditionally laboratory-based instrument technologies that enable miniaturization to a field-portable configuration. The implications of these advancements extend past traditional terrestrial field geology and into planetary surface exploration. With tools that will allow for real-time geochemical analysis, an astronaut can better develop a series of working hypotheses that are testable during surface science operations. One such technology is x-ray fluorescence (XRF). Traditionally used in a laboratory configuration, these instruments have now been developed and marketed commercially in a field-portable mode. We examine this technology in the context of geologic sample analysis and discuss current and future plans for instrument deployment. We also discuss the development of the Chromatic Mineral Identification and Surface Texture (CMIST) instrument at the NASA Goddard Space Flight Center (GSFC). Testing is taking place in conjunction with the RIS4E (Remote, In Situ, and Synchrotron Studies for Science and Exploration) SSERVI (Solar System Exploration and Research Virtual Institute) team activities, including field testing at Kilauea Volcano, HI..

GEOCHEMICAL AND ISOTOPIC CONSTRAINTS ON GROUND-WATER FLOW DIRECTIONS, MIXING AND RECHARGE AT YUCCA MOUNTAIN, NEVADA

International Nuclear Information System (INIS)

A. Meijer; E. Kwicklis

2000-01-01

This analysis is governed by the Office of Civilian Radioactive Waste Management (OCRWM) Analysis and Modeling Report Development Plan entitled ''Geochemical and Isotopic Constraints on Groundwater Flow Directions, Mixing and Recharge at Yucca Mountain'' (CRWMS M and O 1999a). As stated in this Development Plan, the purpose of the work is to provide an analysis of groundwater recharge rates, flow directions and velocities, and mixing proportions of water from different source areas based on groundwater geochemical and isotopic data. The analysis of hydrochemical and isotopic data is intended to provide a basis for evaluating the hydrologic system at Yucca Mountain independently of analyses based purely on hydraulic arguments. Where more than one conceptual model for flow is possible, based on existing hydraulic data, hydrochemical and isotopic data may be useful in eliminating some of these conceptual models. This report documents the use of geochemical and isotopic data to constrain rates and directions of groundwater flow near Yucca Mountain and the timing and magnitude of recharge in the Yucca Mountain vicinity. The geochemical and isotopic data are also examined with regard to the possible dilution of groundwater recharge from Yucca Mountain by mixing with groundwater downgradient from the potential repository site. Specifically, the primary tasks of this report, as listed in the AMR Development Plan (CRWMS M and O 1999a), consist of the following: (1) Compare geochemical and isotopic data for perched and pore water in the unsaturated zone with similar data from the saturated zone to determine if local recharge is present in the regional groundwater system; (2) Determine the timing of the recharge from stable isotopes such as deuterium ( 2 H) and oxygen-18 ( 18 O), which are known to vary over time as a function of climate, and from radioisotopes such as carbon-14 ( 14 C) and chlorine-36 ( 36 Cl); (3) Determine the magnitude of recharge from relatively

Geochemical and physical drivers of microbial community structure in hot spring ecosystems

Science.gov (United States)

Havig, J. R.; Hamilton, T. L.; Boyd, E. S.; Meyer-Dombard, D. R.; Shock, E.

2012-12-01

Microbial communities in natural systems are typically characterized using samples collected from a single time point, thereby neglecting the temporal dynamics that characterize natural systems. The composition of these communities obtained from single point samples is then related to the geochemistry and physical parameters of the environment. Since most microbial life is adapted to a relatively narrow ecological niche (multiplicity of physical and chemical parameters that characterize a local habitat), these assessments provide only modest insight into the controls on community composition. Temporal variation in temperature or geochemical composition would be expected to add another dimension to the complexity of niche space available to support microbial diversity, with systems that experience greater variation supporting a greater biodiversity until a point where the variability is too extreme. . Hot springs often exhibit significant temporal variation, both in physical as well as chemical characteristics. This is a result of subsurface processes including boiling, phase separation, and differential mixing of liquid and vapor phase constituents. These characteristics of geothermal systems, which vary significantly over short periods of time, provide ideal natural laboratories for investigating how i) the extent of microbial community biodiversity and ii) the composition of those communities are shaped by temporal fluctuations in geochemistry. Geochemical and molecular samples were collected from 17 temporally variable hot springs across Yellowstone National Park, Wyoming. Temperature measurements using data-logging thermocouples, allowing accurate determination of temperature maximums, minimums, and ranges for each collection site, were collected in parallel, along with multiple geochemical characterizations as conditions varied. There were significant variations in temperature maxima (54.5 to 90.5°C), minima (12.5 to 82.5°C), and range (3.5 to 77.5°C) for

Sharp fronts within geochemical transport problems

International Nuclear Information System (INIS)

Grindrod, P.

1995-01-01

The authors consider some reactive geochemical transport problems in groundwater systems. When incoming fluid is in disequilibrium with the mineralogy sharp transition fronts may develop. They show that this is a generic property for a class of systems where the timescales associated with reaction and diffusion phenomena are much shorter than those associated with advective transport. Such multiple timescale problems are relevant to a variety of processes in natural systems: mathematically methods of singular perturbation theory reduce the dimension of the problems to be solved locally. Furthermore, they consider how spatial heterogeneous mineralogy can impact upon the propagation of sharp geochemical fronts. The authors developed an asymptotic approach in which they solve equations for the evolving geometry of the front and indicate how the non-smooth perturbations due to natural heterogeneity of the mineralogy on underlying ground water flow field are balanced against the smoothing effect of diffusion/dispersive processes. Fronts are curvature damped, and the results here indicate the generic nature of separate front propagation within both model (idealized) and natural (heterogeneous) geochemical systems

UMTRA Project water sampling and analysis plan, Gunnison, Colorado. Revision 2

International Nuclear Information System (INIS)

1995-09-01

Surface remedial action at the Gunnison Uranium Mill Tailings Remedial Action Project site began in 1992; completion is expected in 1995. Ground water and surface water will be sampled semiannually at the Gunnison processing site (GUN-01) and disposal site (GUN-08). Results of previous water sampling at the Gunnison processing site indicate that ground water in the alluvium is contaminated by the former uranium processing activities. Background ground water conditions have been established in the uppermost aquifer (Tertiary gravels) at the Gunnison disposal site. Semiannual water sampling is scheduled for the spring and fall. Water quality sampling is conducted at the processing site (1) to ensure protection of human health and the environment, (2) for ground water compliance monitoring during remedial action construction, and (3) to define the extent of contamination. At the processing site, the frequency and duration of sampling will be dependent upon the nature and extent of residual contamination and the compliance strategy chosen. The monitor well locations provide a representative distribution of sampling points to characterize ground water quality and ground water flow conditions in the vicinity of the sites. The list of analytes has been modified with time to reflect constituents that are related to uranium processing activities and the parameters needed for geochemical evaluation

Sulfur Geochemical Analysis and Interpretation with ChemCam on the Curiosity Rover

Science.gov (United States)

Clegg, S. M.; Anderson, R. B.; Frydenvang, J.; Forni, O.; Newsom, H. E.; Blaney, D. L.; Maurice, S.; Wiens, R. C.

2017-12-01

The Curiosity rover has encountered many forms of sulfur including calcium sulfate veins [1], hydrated Mg sulfates, and Fe sulfates along the traverse through Gale crater. A new SO3 calibration model for the remote Laser-Induced Breakdown Spectroscopy (LIBS) technique used by the ChemCam instrument enables improved quantitative analysis of SO3, which has not been previously reported by ChemCam on a routine or quantitative basis. In this paper, the details of this new LIBS calibration model will be described and applied to many disparate Mars targets. Among them, Mavor contains a calcium sulfate vein surrounded by bedrock. In contrast, Jake M. is a float rock, Wernecke is a bedrock, Cumberland and Windjana are drill targets. In 2015 the ChemCam instrument team completed a re-calibration of major elements based on a significantly expanded set of >500 geochemical standards using the ChemCam testbed at Los Alamos National Laboratory [2]. In addition to these standards, the SO3 compositional range was recently extended with a series of doped samples containing various mixtures of Ca- and Mg-sulfate with basalt BHVO2. Spectra from these standards were processed per [4]. Calibration and Mars spectra were converted to peak-area-summed LIBS spectra that enables the SO3 calibration. These peak-area spectra were used to generate three overlapping partial least squares (PLS1) calibration sub-models as described by Anderson et al. [3, 5]. ChemCam analysis of Mavor involved a 3x3 raster in which locations 5 and 6 primarily probed Ca-sulfate material. The new ChemCam SO3 compositions for Mavor 5 and Mavor 6 are 48.6±1.2 and 50.3±1.2 wt% SO3, respectively. The LIBS spectra also recorded the presence of other elements that are likely responsible for the departure from pure Ca-sulfate chemistry. On the low-abundance side, the remaining 7 Mavor locations, Jake M., Cumberland, Windjana, and Wernecke all contain much lower SO3, between 1.4±0.5 wt% and 2.3±0.3 wt% SO3. [1] Nachon et

Magnetic and geochemical characterization of Andosols developed on basalts in the Massif Central, France

Science.gov (United States)

Grison, Hana; Petrovsky, Eduard; Stejskalova, Sarka; Kapicka, Ales

2015-05-01

Identification of Andosols is primarily based upon the content of their colloidal constituents—clay and metal-humus complexes—and on the determining of andic properties. This needs time and cost-consuming geochemical analyses. Our primary aim of this study is to describe the magnetic and geochemical properties of soils rich in iron oxides derived from strongly magnetic volcanic basement (in this case Andosols). Secondary aim is to explore links between magnetic and chemical parameters of andic soils with respect to genesis factors: parent material age, precipitation, and thickness of the soil profile. Six pedons of andic properties, developed on basaltic lavas, were analyzed down to parent rock by a set of magnetic and geochemical methods. Magnetic data of soil and rock samples reflect the type, concentration, and particle-size distribution of ferrimagnetic minerals. Geochemical data include soil reaction (pH in H2O), cation exchange capacity, organic carbon, and different forms of extractable iron and aluminum content. Our results suggest the following: (1) magnetic measurements of low-field mass-specific magnetic susceptibility can be a reliable indicator for estimating andic properties, and in combination with thermomagnetic curves may be suitable for discriminating between alu-andic and sil-andic subtypes. (2) In the studied Andosols, strong relationships were found between (a) magnetic grain-size parameters, precipitation, and exchangeable bases; (b) concentration of ferrimagnetic particles and degree of crystallization of free iron; and (c) parameters reflecting changes in magneto-mineralogy and soil genesis (parent material age + soil depth).

Analysis of Frankincense in Archaeological Samples by Gas Chromatography-Mass Spectrometry

International Nuclear Information System (INIS)

Mathe, C.; Archier, P.; Vieillescazes, C.; Connan, J.; Mouton, M.

2007-01-01

Four archaeological samples, unearthed from Qana in Yemen were analysed by analytical technique, currently applied in the field of petroleum geochemistry, and by gas chromatography coupled with a mass spectrometer (GC-MS). Sample no 1286 comes from a burned warehouse and samples no 964, 963 and 962 from the central sanctuary. These specimens were probably exposed to a heating source. In each case olibanum resin was identified according to the presence of their chemical markers corresponding to α-, β-boswellic and lupeolic acids (3α-hydroxy-olean-12-en-24-oic, 3α-hydroxy-urs-12-en-24-oic and 3α-hydroxy-lup-20(29)en-24-oic acids) and their respective O-acetyled derivatives (3α- O-acetyl -olean-12-en-24-oic, 3α-O-acetyl-urs-12-en-24-oic and 3α-O-acetyl-lup-20(29)-en-24-oic acids). Concerning the thermal degradation state of samples, the GC-MS results are in agreement with the geochemical ones. Sample no 1286 and 964 correspond to ageing incense which has not undergone any heating action and are consequently relatively well preserved. Lastly, samples no 963 and 962 are thermally degraded resins and their gross composition data permits to conclude that sample no 963 is only partially burnt while sample no 962 has been much more degraded

Significance of geochemical characterization to performance at Yucca Mountain, Nevada

International Nuclear Information System (INIS)

Simmons, A.M.

1993-01-01

The U.S. concept for permanent disposal of high-level radioactive waste resembles those of other countries in that it relies upon burial in a deep geologic medium. This concept relies upon multiple barriers to retard transport of radionuclides to the accessible environment; those barriers consist of the waste form, waste container, engineered barrier system (including possible backfill) and retardant properties of the host rock. Because mobilization of radionuclides is fundamentally a geochemical problem, an understanding of past, present, and future geochemical processes is a requisite part of site characterization studies conducted by the U.S. Department of Energy at Yucca Mountain, Nevada. Geochemical information is needed for evaluating three favorable conditions (the rates of geochemical processes, conditions that promote precipitation or sorption of radionuclides or prohibit formation of colloids, and stable mineral assemblages) and four potentially adverse conditions of the site (groundwater conditions that could increase the chemical reactivity of the engineered barried system or reduce sorption, potential for gaseous radionuclide movement, and oxidizing groundwaters) for key issues of radionuclide release, groundwater quality, and stability of the geochemical environment. Preliminary results of long-term heating experiments indicate that although zeolites can be modified by long-term, low temperature reactions, their beneficial sorptive properties will not be adversely affected. Mineral reactions will be controlled by the aqueous activity of silica in groundwater with which the minerals are in contact. Geochemical barriers alone may satisfy release requirements to the accessible environment for many radionuclides; however, additional site specific geochemical and mineralogical data are needed to test existing and future radionuclide transport models

Lead Isotopes in Olivine-Phyric Shergottite Tissint: Implications for the Geochemical Evolution of the Shergottite Source Mantle

Science.gov (United States)

Moriwaki, R.; Usui, T.; Simon, J. I.; Jones, J. H.; Yokoyama, T.

2015-01-01

Geochemically-depleted shergottites are basaltic rocks derived from a martian mantle source reservoir. Geochemical evolution of the martian mantle has been investigated mainly based on the Rb-Sr, Sm-Nd, and Lu-Hf isotope systematics of the shergottites [1]. Although potentially informative, U-Th- Pb isotope systematics have been limited because of difficulties in interpreting the analyses of depleted meteorite samples that are more susceptible to the effects of near-surface processes and terrestrial contamination. This study conducts a 5-step sequential acid leaching experiment of the first witnessed fall of the geochemically-depleted olivinephyric shergottite Tissint to minimize the effect of low temperature distrubence. Trace element analyses of the Tissint acid residue (mostly pyroxene) indicate that Pb isotope compositions of the residue do not contain either a martian surface or terrestrial component, but represent the Tissint magma source [2]. The residue has relatively unradiogenic initial Pb isotopic compositions (e.g., 206Pb/204Pb = 10.8136) that fall within the Pb isotope space of other geochemically-depleted shergottites. An initial µ-value (238U/204Pb = 1.5) of Tissint at the time of crystallization (472 Ma [3]) is similar to a time-integrated mu- value (1.72 at 472 Ma) of the Tissint source mantle calculated based on the two-stage mantle evolution model [1]. On the other hand, the other geochemically-depleted shergottites (e.g., QUE 94201 [4]) have initial µ-values of their parental magmas distinctly lower than those of their modeled source mantle. These results suggest that only Tissint potentially reflects the geochemical signature of the shergottite mantle source that originated from cumulates of the martian magma ocean

Coupling of transport and geochemical models

International Nuclear Information System (INIS)

Noy, D.J.

1985-01-01

This contract stipulated separate pieces of work to consider mass transport in the far-field of a repository, and more detailed geochemical modelling of the groundwater in the near-field. It was envisaged that the far-field problem would be tackled by numerical solutions to the classical advection-diffusion equation obtained by the finite element method. For the near-field problem the feasibility of coupling existing geochemical equilibrium codes to the three dimensional groundwater flow codes was to be investigated. This report is divided into two sections with one part devoted to each aspect of this contract. (author)

Integrated geophysical-geochemical methods for archaeological prospecting

OpenAIRE

Persson, Kjell

2005-01-01

A great number of field measurements with different methods and instruments were conducted in attempts to develop a method for an optimal combination of various geochemical and geophysical methods in archaeological prospecting. The research presented in this thesis focuses on a study of how different anthropogenic changes in the ground can be detected by geochemical and geophysical mapping and how the results can be presented. A six-year pilot project, Svealand in Vendel and Viking periods (S...

Retention/sorption and geochemical modelling

Energy Technology Data Exchange (ETDEWEB)

Arcos, D.; Grandia, F.; Domenech, C. [Enviros Spain, S.L., Barcelona (Spain); SCK-CEN, Mol (Belgium); Sellin, P. [SKB - Swedish Nuclear Fuel and Waste Management, SE, Stockholm (Sweden); Hunter, F.M.I.; Bate, F.; Heath, T.G.; Hoch, A. [Serco Assurance, Oxfordshire (United Kingdom); Werme, L.O. [SKB - Svensk Karnbranslehantering AB, Stockholm (Sweden); Bruggeman, C.; Maes, I.A.; Breynaert, E.; Vancluysen, J. [Leuven Katholieke Univ., Lab. for Colloid Chemistry (Belgium); Montavon, G.; Guo, Z. [Ecole des Mines, 44 - Nantes (France); Riebe, B.; Bunnenberg, C.; Meleshyn, A. [Leibniz Univ. Hannover, Zentrum fur Strahlenschutz und Radiookologie, Hannover (Germany); Dultz, S. [Leibniz Univ. Hannover, Institut fur Bodenkunde, Hannover (Germany)

2007-07-01

This session gathers 4 articles dealing with: the long-term geochemical evolution of the near field of a KBS-3 HLNW repository: insights from reactive transport modelling (D. Arcos, F. Grandia, C. Domenech, P. Sellin); the investigation of iron transport into bentonite from anaerobically corroding steel: a geochemical modelling study (F.M.I. Hunter, F. Bate, T.G. Heath, A. Hoch, L.O. Werme); SeO{sub 3}{sup 2-} adsorption on conditioned Na-illite: XAS spectroscopy, kinetics, surface complexation model and influence of compaction (C. Bruggeman, A. Maes, G. Montavon, E. Breynaert, Z. Guo, J. Vancluysen); the influence of temperature and gamma-irradiation on the anion sorption capacity of modified bentonites (B. Riebe, C. Bunnenberg, A. Meleshyn, S. Dultz)

Geochemical reconnaissance for uranium in the Palmyrides region of central Syria

International Nuclear Information System (INIS)

Jubeli, Y.M.

1990-01-01

An account is given of the application of multielement reconnaissance rock chemistry, coupled with ground scintillation γ-ray measurements, to the investigation of the dispersion patterns of uranium and other major and trace elements in the rocks of the arid Palmyrides region of central Syria. The region is underlain by 10 km of sediments that accumulated in an interplatform depression during the Mesozoic and Caenozoic. Uranium and associated elements were syngenetically incorporated into the Upper Cretaceous and Lower Palaeogene sediments - especially phosphorites, which are well represented in the region. The oxidizing environment of the region has facilitated the subsequent geochemical redistribution of uranium. In the investigation more than 400 lithogeochemical samples collected from an area of approximately 9000 km 2 were analysed for over 30 elements. The resulting data were interpreted with the aid of univariate and multivariate statistical methods and the areal distribution of uranium, its associated elements, multivariate geochemical functions and factor scores were mapped with the use of computer graphics. Anomalies of U are accompanied by concentrations of As, Se, V, Mo, Zn, Cd, Cu, Ni and P in various combinations. The highest U concentrations are found in the Upper Cretaceous, which contains a high proportion of phosphatic rocks; younger sediments contain progressively less U. Uranium anomalies close to faults, which have provided conduits for wider U migration, are superimposed on this pattern. Lithogeochemical methods thus define geochemical dispersion patterns with good contrast and delineate areas for further investigation. (author)

Quantification of source-term profiles from near-field geochemical models

International Nuclear Information System (INIS)

McKinley, I.G.

1985-01-01

A geochemical model of the near-field is described which quantitatively treats the processes of engineered barrier degradation, buffering of aqueous chemistry by solid phases, nuclide solubilization and transport through the near-field and release to the far-field. The radionuclide source-terms derived from this model are compared with those from a simpler model used for repository safety analysis. 10 refs., 2 figs., 2 tabs

Sampling and chemical analysis in environmental samples around Nuclear Power Plants and some environmental samples

Energy Technology Data Exchange (ETDEWEB)

Cho, Yong Woo; Han, Man Jung; Cho, Seong Won; Cho, Hong Jun; Oh, Hyeon Kyun; Lee, Jeong Min; Chang, Jae Sook [KORTIC, Taejon (Korea, Republic of)

2002-12-15

Twelve kinds of environmental samples such as soil, seawater, underground water, etc. around Nuclear Power Plants(NPPs) were collected. Tritium chemical analysis was tried for the samples of rain water, pine-needle, air, seawater, underground water, chinese cabbage, a grain of rice and milk sampled around NPPs, and surface seawater and rain water sampled over the country. Strontium in the soil that sere sampled at 60 point of district in Korea were analyzed. Tritium were sampled at 60 point of district in Korea were analyzed. Tritium were analyzed in 21 samples of surface seawater around the Korea peninsular that were supplied from KFRDI(National Fisheries Research and Development Institute). Sampling and chemical analysis environmental samples around Kori, Woolsung, Youngkwang, Wooljin Npps and Taeduk science town for tritium and strontium analysis was managed according to plans. Succeed to KINS after all samples were tried.

Geochemical Characteristics of the Gyeongju LILW Repository II. Rock and Minera

International Nuclear Information System (INIS)

Kim, Geon Young; Koh, Yong Kwon; Choi, Byoung Young; Shin, Seon Ho; Kim, Doo Haeng

2008-01-01

Geochemical study on the rocks and minerals of the Gyeongju low and intermediate level waste repository was carried out in order to provide geochemical data for the safety assessment and geochemical modeling. Polarized microscopy, X-ray diffraction method, chemical analysis for the major and trace elements, scanning electron microscopy (SEM), and stable isotope analysis were applied. Fracture zones are locally developed with various degrees of alteration in the study area. The study area is mainly composed of granodiorite and diorite and their relation is gradational in the field. However, they could be easily distinguished by their chemical property. The granodiorite showed higher Sig 2 content and lower MgO and Fe 2 O 3 contents than the diorite. Variation trends of the major elements of the granodiorite and diorite were plotted on the same line according to the increase of Sig 2 content suggesting that they were differentiated from the same magma. Spatial distribution of the various elements showed that the diorite region had lower Sig 2 , Al 2 O 3 , Na 2 O and K 2 O contents, and higher CaO, Fe 2 O 3 contents than the granodiorite region. Especially, because the differences in the CaO and Na 2 O distribution were most distinct and their trends were reciprocal, the chemical variation of the plagioclase of the granitic rocks was the main parameter of the chemical variation of the host rocks in the study area. Identified fracture-filling minerals from the drill core were montmorillonite, zeolite minerals, chlorite, illite, calcite and pyrite. Especially pyrite and laumontite, which are known as indicating minerals of hydrothermal alteration, were widely distributed in the study area indicating that the study area was affected by mineralization and/or hydrothermal alteration. Sulfur isotope analysis for the pyrite and oxygen-hydrogen stable isotope analysis for the clay minerals indicated that they were originated from the magma. Therefore, it is considered that

Relation between the geochemical environment and disease incidence rate. A case study the Island Krk in the Adriatic Sea, Croatia

International Nuclear Information System (INIS)

Kutle, A.; Obhodas, J.; Valkovic, V.

2006-01-01

It has been observed that among the seven municipalities of the Island of Krk the three in the central part of the island have increased disease incidence rates for the five groups of diseases: (a) neoplasm, (b) diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism, (c) endocrine, nutritional and metabolic diseases, (d) mental and behavioral disorders and (e) diseases of the circulatory system. One of the etiological factors is assumed to be the influence of the geochemical environment. The average element concentration values of six trace elements (Mn, Fe, Ni, Cu, Zn and As) for the geochemical environment in the individual municipalities were determined by XRF analyses of soil, plant, potable water and hair samples. The data on disease incidence rates for the individual municipalities, from 1997 to 2001, have been obtained from the Public Health Institution in charge of monitoring population health on the island. Diseases' groups have been defined by the WHO methodology. The GPS-GIS methodology was used to obtain maps of trace elements in different matrices and disease incidence distributions. Data analyses were performed by multivariate statistical methods (principal component analysis and cluster analysis). It has been shown that the concentration levels of the elements could be related to disease incidence rates. (author)

Large sample neutron activation analysis of a reference inhomogeneous sample

International Nuclear Information System (INIS)

Vasilopoulou, T.; Athens National Technical University, Athens; Tzika, F.; Stamatelatos, I.E.; Koster-Ammerlaan, M.J.J.

2011-01-01

A benchmark experiment was performed for Neutron Activation Analysis (NAA) of a large inhomogeneous sample. The reference sample was developed in-house and consisted of SiO 2 matrix and an Al-Zn alloy 'inhomogeneity' body. Monte Carlo simulations were employed to derive appropriate correction factors for neutron self-shielding during irradiation as well as self-attenuation of gamma rays and sample geometry during counting. The large sample neutron activation analysis (LSNAA) results were compared against reference values and the trueness of the technique was evaluated. An agreement within ±10% was observed between LSNAA and reference elemental mass values, for all matrix and inhomogeneity elements except Samarium, provided that the inhomogeneity body was fully simulated. However, in cases that the inhomogeneity was treated as not known, the results showed a reasonable agreement for most matrix elements, while large discrepancies were observed for the inhomogeneity elements. This study provided a quantification of the uncertainties associated with inhomogeneity in large sample analysis and contributed to the identification of the needs for future development of LSNAA facilities for analysis of inhomogeneous samples. (author)

Actual stage of organic geochemical knowledge from Campos and Espirito Santo basins, Brazil

International Nuclear Information System (INIS)

Gaglianone, P.C.; Trindade, L.A.F.

1987-01-01

Campos and Espirito Santo basins display several similar geochemical aspects. The microbial and other degradation processes caused changes in the composition of the oils in the reservoir rocks. The oils are biodegraded in different degrees, with the reservoir temperature developing an important role in the control of the biodegradation process. The migration pathway model is similar for Campos and Espirito Santo basins, involving the upward secondary migration through a window in the evaporitic seals. The oils passed to the marine sequence where migration and accumulation were controlled by faults, regional unconformities and by reservoirs. The geochemical correlation of oils are realized by gaseous and liquid chromatography analysis, carbon isotopes and biolabelled compounds. (author)

Geochemical controls on groundwater chemistry in shales

International Nuclear Information System (INIS)

Von Damm, K.L.

1989-01-01

The chemistry of groundwaters is one of the most important parameters in determining the mobility of species within a rock formation. A three pronged approach was used to determine the composition of, and geochemical controls, on groundwaters specifically within shale formations: (1) available data were collected from the literature, the US Geological Survey WATSTORE data base, and field sampling, (2) the geochemical modeling code EQ3/6 was used to simulate interaction of various shales and groundwaters, and (3) several types of shale were reacted with synthetic groundwaters in the laboratory. The comparison of model results to field and laboratory data provide a means of validating the models, as well as a means of deconvoluting complex field interactions. Results suggest that groundwaters in shales have a wide range in composition and are primarily of the Na-Cl-HCO 3 - type. The constancy of the Na:Cl (molar) ratio at 1:1 and the Ca:Mg ratio from 3:1 to 1:1 suggests the importance of halite and carbonates in controlling groundwater compositions. In agreement with the reaction path modeling, most of the groundwaters are neutral to slightly alkaline at low temperatures. Model and experimental results suggest that reaction (1) at elevated temperatures, or (2) in the presence of oxygen will lead to more acidic conditions. Some acetate was found to be produced in the experiments; depending on the constraints applied, large amounts of acetate were produced in the model results. 13 refs., 1 tab

Sulfide geochemical survey in Dawahan, Larap, Camarines Norte (Southern Luzon), Philippines

International Nuclear Information System (INIS)

Santos, G. Jr.

1979-07-01

Sulfide geochemical activation analysis survey was conducted in Southern Luzon, Philippines. Trace elements in the rocks of Dawahan, Larap, Camarines Norte, particularly in the sulfide fraction of the rocks were determined and correlated in the search for mineral deposits in the project area. The study has shown that the Cu, V, Co, Pb, Mn, Zn, Ni, Au, Ag and As distributions in Dawahan are log normal with Cu, As and V having an excess of low values. There is a direct relationship between the mineralizations of Ag and Pb with Cu mineralization. Fair geochemical correlations were observed between Cu-Zn, Cu-As and Cu-Co. Low negative or inverse correlation exists between Cu-Mn, Cu-V and Cu-Au. Silver is a good pathfinder for copper deposits in Dawahan and adjacent areas and most probably including the Paracale mining district

Geochemical behaviour of natural uranium-series nuclides in geological formation

International Nuclear Information System (INIS)

Yamakawa, Minoru

1991-01-01

Recent research and investigation show that the Tono uranium deposit and its natural uranium-series nuclides have been preserved, without any significant changes like re-migration or reconcentration, throughout geological events such as upheaval-submergence, marine transgression-regression, and faulting which can readily change geological, hydrogeological, and geochemical conditions. This situation might have come about as a result of being kept in a geometrical closure system, with reducing and milk alkalic geochemical conditions, from the hydrogeological and geochemical point of view. (author)

Notes on the geochemical survey for uranium in Mindoro Island, Philippines

International Nuclear Information System (INIS)

Santos, G. Jr.; Fernandez, L.G.; Villamater, D.T.; Seguis, J.E.; Ibe, M.G.

1981-03-01

Geochemical reconnaisance using stream sediment and heavy-mineral concentrates panned from coarse alluvium has been carried out in Mindoro Island, one of the oldest and diverse geologic terrains in the Philippines. A total of 135 selected sampling points situated near accessible areas along the periphery of the island were sampled. The samples were collected at a density of one sample per 53 sq. km. A set minus 80 mesh stream sediment fraction and heavy-mineral concentrates was obtained from each sampling point. Mobile or extractable and total uranium were determined. A large uranium anomaly was delineated over the Carboniferous Mindoro Metamorphics as well as in areas underlain by Early Tertiary sedimentary formations. Another group of anomalies were outlined in the southern part of the island underlain by Jurassic Mansalay Formation and Early to Middle Tertiary sedimentary rocks with associated limestone and coal measures. (author)

Application of Fractal Technique for Analysis of Geophysical - Geochemical Databases in Tekieh Pb-Zn Ore Deposit (SE of Arak)

International Nuclear Information System (INIS)

Mehrnia, S.R.

2017-01-01

In this research, two statistical techniques that consist of classical and fractal equations (Mandelbrot, 2005) were applied in geochemical (Torkashvand et al., 2009) and geophysical (Jafari, 2007) databases for obtaining the linear and nonlinear distributions of geochemical elements (Tekieh Pb-Zn content) in association with resistivity variations and induction polarization measurements (Calagari, 2010). According to linear statistical techniques (Torkashvand et al., 2009), the main central parameters such as mean, median and mode in addition to variances and standard deviations as distribution tendencies could be used for obtaining the regression coefficients of the databases. However, in fractal statistics, a reliable regression between geo electrical - geochemical anomalies should be calculated based on measuring the fractal dimensional variations in the recursive patterns (Mehrnia, 2013). In practice, the Area-Concentration equations (Mandelbrot, 2005) were applied in resistivity, induction polarization, Pb and Zn datasets for achieving the nonlinear relationships in anomalous regions which were characterized by increasing in regression coefficients with more spatial correlation of the variable than linear statistics (Mehrnia, 2013).

Geochemical evidence for diversity of dust sources in the southwestern United States

Science.gov (United States)

Reheis, M.C.; Budahn, J.R.; Lamothe, P.J.

2002-01-01

Several potential dust sources, including generic sources of sparsely vegetated alluvium, playa deposits, and anthropogenic emissions, as well as the area around Owens Lake, California, affect the composition of modern dust in the southwestern United States. A comparison of geochemical analyses of modern and old (a few thousand years) dust with samples of potential local sources suggests that dusts reflect four primary sources: (1) alluvial sediments (represented by Hf, K, Rb, Zr, and rare-earth elements, (2) playas, most of which produce calcareous dust (Sr, associated with Ca), (3) the area of Owens (dry) Lake, a human-induced playa (As, Ba, Li, Pb, Sb, and Sr), and (4) anthropogenic and/or volcanic emissions (As, Cr, Ni, and Sb). A comparison of dust and source samples with previous analyses shows that Owens (dry) Lake and mining wastes from the adjacent Cerro Gordo mining district are the primary sources of As, Ba, Li, and Pb in dusts from Owens Valley. Decreases in dust contents of As, Ba, and Sb with distance from Owens Valley suggest that dust from southern Owens Valley is being transported at least 400 km to the east. Samples of old dust that accumulated before European settlement are distinctly lower in As, Ba, and Sb abundances relative to modern dust, likely due to modern transport of dust from Owens Valley. Thus, southern Owens Valley appears to be an important, geochemically distinct, point source for regional dust in the southwestern United States. Copyright ?? 2002 Elsevier Science Ltd.

Seeps and springs sampling and analysis plant for the Environmental Monitoring Plan at Waste Area Grouping 6, Oak Ridge National Laboratory, Oak Ridge, Tennessee

Energy Technology Data Exchange (ETDEWEB)

NONE

1995-09-01

This Sampling and Analysis Plan addresses the monitoring, sampling, and analysis activities that will be conducted at seeps and springs and at two french drain outlets in support of the Environmental Monitoring Plan for Waste Area Grouping (WAG) 6. WAG 6 is a shallow-land-burial disposal facility for low-level radioactive waste at Oak Ridge National Laboratory, a research facility owned by the U.S. Department of Energy and operated by Lockheed Martin Energy System, Inc. Initially, sampling will be conducted at as many as 15 locations within WAG 6 (as many as 13 seeps and 2 french drain outlets). After evaluating the results obtained and reviewing the observations made by field personnel during the first round of sampling, several seeps and springs will be chosen as permanent monitoring points, together with the two french drain outlets. Baseline sampling of these points will then be conducted quarterly for 1 year (i.e., four rounds of sampling after the initial round). The samples will be analyzed for various geochemical, organic, inorganic, and radiological parameters. Permanent sampling points having suitable flow rates and conditions may be outfitted with automatic flow-monitoring equipment. The results of the sampling and flow-monitoring efforts will help to quantify flux moving across the ungauged perimeter of the site and will help to identify changes in releases from the contaminant sources.

Seeps and springs sampling and analysis plant for the Environmental Monitoring Plan at Waste Area Grouping 6, Oak Ridge National Laboratory, Oak Ridge, Tennessee

International Nuclear Information System (INIS)

1995-09-01

This Sampling and Analysis Plan addresses the monitoring, sampling, and analysis activities that will be conducted at seeps and springs and at two french drain outlets in support of the Environmental Monitoring Plan for Waste Area Grouping (WAG) 6. WAG 6 is a shallow-land-burial disposal facility for low-level radioactive waste at Oak Ridge National Laboratory, a research facility owned by the U.S. Department of Energy and operated by Lockheed Martin Energy System, Inc. Initially, sampling will be conducted at as many as 15 locations within WAG 6 (as many as 13 seeps and 2 french drain outlets). After evaluating the results obtained and reviewing the observations made by field personnel during the first round of sampling, several seeps and springs will be chosen as permanent monitoring points, together with the two french drain outlets. Baseline sampling of these points will then be conducted quarterly for 1 year (i.e., four rounds of sampling after the initial round). The samples will be analyzed for various geochemical, organic, inorganic, and radiological parameters. Permanent sampling points having suitable flow rates and conditions may be outfitted with automatic flow-monitoring equipment. The results of the sampling and flow-monitoring efforts will help to quantify flux moving across the ungauged perimeter of the site and will help to identify changes in releases from the contaminant sources

Geochemical and isotopic determination of deep groundwater contributions and salinity to the shallow groundwater and surface water systems, Mesilla Basin, New Mexico, Texas, and Mexico

Science.gov (United States)

Robertson, A.; Carroll, K. C.; Kubicki, C.; Purtshert, R.

2017-12-01

The Mesilla Basin/Conejos-Médanos aquifer system, extending from southern New Mexico to Chihuahua, Mexico, is a priority transboundary aquifer under the 2006 United States­-Mexico Transboundary Aquifer Assessment Act. Declining water levels, deteriorating water quality, and increasing groundwater use by municipal, industrial, and agricultural users on both sides of the international border raise concerns about long-term aquifer sustainability. Relative contributions of present-day and "paleo" recharge to sustainable fresh groundwater yields has not been determined and evidence suggests that a large source of salinity at the distal end of the Mesilla Basin is saline discharge from deep groundwater flow. The magnitude and distribution of those deep saline flow paths are not determined. The contribution of deep groundwater to discharge and salinity in the shallow groundwater and surface water of the Mesilla Basin will be determined by collecting discrete groundwater samples and analyzing for aqueous geochemical and isotopic tracers, as well as the radioisotopes of argon and krypton. Analytes include major ions, trace elements, the stable isotopes of water, strontium and boron isotopes, uranium isotopes, the carbon isotopes of dissolved inorganic carbon, noble gas concentrations and helium isotope ratios. Dissolved gases are extracted and captured from groundwater wells using membrane contactors in a process known as ultra-trace sampling. Gas samples are analyzed for radioisotope ratios of krypton by the ATTA method and argon by low-level counting. Effectiveness of the ultra-trace sampling device and method was evaluated by comparing results of tritium concentrations to the krypton-85 content. Good agreement between the analyses, especially in samples with undetectable tritium, indicates that the ultra-trace procedure is effective and confirms that introduction of atmospheric air has not occurred. The geochemistry data indicate a complex system of geochemical

Extreme drought decouples silicon and carbon geochemical linkages in lakes.

Science.gov (United States)

Li, Tianyang; Li, Siyue; Bush, Richard T; Liang, Chuan

2018-09-01

Silicon and carbon geochemical linkages were usually regulated by chemical weathering and organism activity, but had not been investigated under the drought condition, and the magnitude and extent of drought effects remain poorly understood. We collected a comprehensive data set from a total of 13 sampling sites covering the main water body of the largest freshwater lake system in Australia, the Lower Lakes. Changes to water quality during drought (April 2008-September 2010) and post-drought (October 2010-October 2013) were compared to reveal the effects of drought on dissolved silica (DSi) and bicarbonate (HCO 3 - ) and other environmental factors, including sodium (Na + ), pH, electrical conductivity (EC), chlorophyll a (Chl-a), total dissolved solids (TDS), dissolved inorganic nitrogen (DIN), total nitrogen (TN), total phosphorus (TP) and water levels. Among the key observations, concentrations of DSi and DIN were markedly lower in drought than in post-drought period while pH, EC and concentrations of HCO 3 - , Na + , Chl-a, TDS, TN, TP and the ratio TN:TP had inverse trends. Stoichiometric ratios of DSi:HCO 3 - , DSi:Na + and HCO 3 - :Na + were significantly lower in the drought period. DSi exhibited significantly negative relationships with HCO 3 - , and DSi:Na + was strongly correlated with HCO 3 - :Na + in both drought and post-drought periods. The backward stepwise regression analysis that could avoid multicollinearity suggested that DSi:HCO 3 - ratio in drought period had significant relationships with fewer variables when compared to the post-drought, and was better predictable using nutrient variables during post-drought. Our results highlight the drought effects on variations of water constituents and point to the decoupling of silicon and carbon geochemical linkages in the Lower Lakes under drought conditions. Copyright © 2018 Elsevier B.V. All rights reserved.

Lateritinga project: a geochemical orientation study for Amazon lateritic

International Nuclear Information System (INIS)

Costa, M.L. da

1990-01-01

The aim of this project is the development of systematic geochemical orientation survey in lateritic weathered terrain, like those form Amazon Region. The main selected targets (sheets) are: Turiacu, Cajuapara and Serra dos Carajas, with 690 samples collected (soils and lateritic rocks). For the Aurizona-Serra do Pirocaua target (Turiacu sheet), within the purpose of this work, 49 samples were collected in a 100x 200m regular grid. From all samples the fraction minor than 200 mesh was taken to analyses (by XRF, AA, OES, ICP and fire assay) for SiO sub(2), Fe sub(2) O sub(3), TiO sub(2), P sub(2) O sub(5), Sr, Ba, Y, Nb, Zr, Ga, Sc, Ni, Co, Cr, Cu, Mn, V, As, Bi, Pt, Pd, Th, Au and REE, as well for their mineralogy by XRD. The chemical results were submitted to statistical treatment with the Geoquant-software for IBM-compatible microcomputer. (author)

Geochemical and physical properties of soils and shallow sediments at the Savannah River Site

Energy Technology Data Exchange (ETDEWEB)

Looney, B.B.; Eddy, C.A.; Ramdeen, M.; Pickett, J. (Savannah River Lab., Aiken, SC (USA)); Rogers, V. (Soil Conservation Service, Aiken, SC (USA). Savannah River Site Savannah River Lab., Aiken, SC (USA)); Scott, M.T.; Shirley, P.A. (Sirrine Environmental Consultants, Greenville, SC (USA))

1990-08-31

A program to characterize the geochemical and physical properties of the unimpacted soils and shallow sediments at the Savannah River Site (SRS) has been completed. The maximum, minimum, median, standard deviation, and mean values for metals, radionuclides, inorganic anions, organic compounds, and agricultural indicator parameters are summarized for six soil series that were identified as representative of the 29 soil series at SRS. The soils from unimpacted areas of SRS are typical of soils found in moderately aggressive weathering environments, including the southeastern United States. Appendix 8 organic compounds were detected in all samples. Since these constituents are not generally present in soil, this portion of the investigation was intended to assess possible laboratory artifacts. An additional objective of the SRS Soil Study was to determine if the composition of the split spoon sampler biased chemical analysis of the soils. Twenty-five duplicate samples were analyzed for a number of metals, radiological and agricultural parameters, and organics by two laboratories currently contracted with to analyze samples during waste site characterization. In all cases, the absolute values of the average differences are relatively small compared to the overall variability in the population. 31 refs., 14 figs., 48 tabs.

Geochemical and physical properties of soils and shallow sediments at the Savannah River Site

International Nuclear Information System (INIS)

Looney, B.B.; Eddy, C.A.; Ramdeen, M.; Pickett, J.; Rogers, V.; Scott, M.T.; Shirley, P.A.

1990-01-01

A program to characterize the geochemical and physical properties of the unimpacted soils and shallow sediments at the Savannah River Site (SRS) has been completed. The maximum, minimum, median, standard deviation, and mean values for metals, radionuclides, inorganic anions, organic compounds, and agricultural indicator parameters are summarized for six soil series that were identified as representative of the 29 soil series at SRS. The soils from unimpacted areas of SRS are typical of soils found in moderately aggressive weathering environments, including the southeastern United States. Appendix 8 organic compounds were detected in all samples. Since these constituents are not generally present in soil, this portion of the investigation was intended to assess possible laboratory artifacts. An additional objective of the SRS Soil Study was to determine if the composition of the split spoon sampler biased chemical analysis of the soils. Twenty-five duplicate samples were analyzed for a number of metals, radiological and agricultural parameters, and organics by two laboratories currently contracted with to analyze samples during waste site characterization. In all cases, the absolute values of the average differences are relatively small compared to the overall variability in the population. 31 refs., 14 figs., 48 tabs

Analysis of monazite samples

International Nuclear Information System (INIS)

Kartiwa Sumadi; Yayah Rohayati

1996-01-01

The 'monazit' analytical program has been set up for routine work of Rare Earth Elements analysis in the monazite and xenotime minerals samples. Total relative error of the analysis is very low, less than 2.50%, and the reproducibility of counting statistic and stability of the instrument were very excellent. The precision and accuracy of the analytical program are very good with the maximum percentage relative are 5.22% and 1.61%, respectively. The mineral compositions of the 30 monazite samples have been also calculated using their chemical constituents, and the results were compared to the grain counting microscopic analysis

Direct-push geochemical profiling for assessment of inorganic chemical heterogeneity in aquifers

Science.gov (United States)

Schulmeister, M.K.; Healey, J.M.; Butler, J.J.; McCall, G.W.

2004-01-01

Discrete-depth sampling of inorganic groundwater chemistry is essential for a variety of site characterization activities. Although the mobility and rapid sampling capabilities of direct-push techniques have led to their widespread use for evaluating the distribution of organic contaminants, complementary methods for the characterization of spatial variations in geochemical conditions have not been developed. In this study, a direct-push-based approach for high-resolution inorganic chemical profiling was developed at a site where sharp chemical contrasts and iron-reducing conditions had previously been observed. Existing multilevel samplers (MLSs) that span a fining-upward alluvial sequence were used for comparison with the direct-push profiling. Chemical profiles obtained with a conventional direct-push exposed-screen sampler differed from those obtained with an adjacent MLS because of sampler reactivity and mixing with water from previous sampling levels. The sampler was modified by replacing steel sampling components with stainless-steel and heat-treated parts, and adding an adapter that prevents mixing. Profiles obtained with the modified approach were in excellent agreement with those obtained from an adjacent MLS for all constituents and parameters monitored (Cl, NO3, Fe, Mn, DO, ORP, specific conductance and pH). Interpretations of site redox conditions based on field-measured parameters were supported by laboratory analysis of dissolved Fe. The discrete-depth capability of this approach allows inorganic chemical variations to be described at a level of detail that has rarely been possible. When combined with the mobility afforded by direct-push rigs and on-site methods of chemical analysis, the new approach is well suited for a variety of interactive site-characterization endeavors. ?? 2003 Elsevier B.V. All rights reserved.

Geochemical surveys in the United States in relation to health

Energy Technology Data Exchange (ETDEWEB)

Tourtelot, H A

1979-12-11

Geochemical surveys in relation to health may be classified as having one, two or three dimensions. One-dimensional surveys examine relations between concentrations of elements such as Pb in soils and other media and burdens of the same elements in humans, at a given time. The spatial distributions of element concentrations are not investigated. The primary objective of two-dimensional surveys is to map the distributions of element concentrations, commonly according to stratified random sampling designs based on either conceptual landscape units or artificial sampling strata, but systematic sampling intervals have also been used. Political units have defined sample areas that coincide with the units used to accumulate epidemiological data. Element concentrations affected by point sources have also been mapped. Background values, location of natural or technological anomalies and the geographic scale of variation for several elements often are determined. Three-dimensional surveys result when two-dimensional surveys are repeated to detect environmental changes.

Geochemical baseline level and function and contamination of phosphorus in Liao River Watershed sediments of China.

Science.gov (United States)

Liu, Shaoqing; Wang, Jing; Lin, Chunye; He, Mengchang; Liu, Xitao

2013-10-15

The quantitative assessment of P contamination in sediments is a challenge due to sediment heterogeneity and the lacking of geochemical background or baseline levels. In this study, a procedure was proposed to determine the average P background level and P geochemical baseline level (GBL) and develop P geochemical baseline functions (GBF) for riverbed sediments of the Liao River Watershed (LRW). The LRW has two river systems - the Liao River System (LRS) and the Daliao River System (DRS). Eighty-eight samples were collected and analyzed for P, Al, Fe, Ca, organic matter, pH, and texture. The results show that Fe can be used as a better particle-size proxy to construct the GBF of P (P (mg/kg) = 39.98 + 166.19 × Fe (%), R(2) = 0.835, n = 66). The GBL of P was 675 mg/kg, while the average background level of P was 355 mg/kg. Noting that many large cities are located in the DRS watershed, most of the contaminated sites were located within the DRS and the riverbed sediments were more contaminated by P in the DRS watershed than in the LRS watershed. The geochemical background and baseline information of P are of great importance in managing P levels within the LRW. Copyright © 2013 Elsevier Ltd. All rights reserved.

Gamma-ray analysis for U, TH and K on bulk cutting samples from deep wells in the Danish subbasin and the North German basin

International Nuclear Information System (INIS)

Leth Nielsen, B.; Loevborg, L.; Soerensen, P.; Mose, E.

1987-04-01

A total of 1329 bulk cutting samples from deep wells in Denmark were analysed for U, Th and K by laboratory gamma-ray analysis. Contamination of the samples by drilling mud additives, mud solids and fall down was studied by means of a wash down experiment and by comparison with the total gamma-ray response from wire-line logging. It is concluded that the inorganic geochemistry on bulk cutting samples must be applied with great caution. The data are useful for geochemical characterization of well sections and for regional geochemical correlation. Radioelement abundance logs and radioelement ratio logs are presented from 3 wells in the Danish Subbasin and 2 wells in the North German Basin. The radioelement geochemistry is discussed for the successive lithostratigraphical units and a reference radio element profile is established for the central part of the Danish Subbasin. Finally, a model describing the relationship between common lithofacies and their U content and Th/U ratio is suggested. The model deliniates the depositional environment and the relative distances to the provenance areas. It is concluded that 1) Uranium is mobile during deposition, but since then it is fixed by stable mineral phases at depth. 2) Thorium reflects source area characteristics and that any available ions are readily adsorped by clay minerals. Thorium anomalies may thus serve as lithostratigraphical markers. 3) Potassium occurs in unstable rock forming mineral phases. The present distribution is controlled not only by the clastic mineral assemblage, but also by the diagenetic processes through geologic time. 33 refs. (author)

Gamma-ray analysis for U, Th and K on bulk cutting samples from deep wells in the Danish Subbasin and the North German Basin

International Nuclear Information System (INIS)

Lovborg, L.

1987-07-01

A total of 1329 bulk cutting samples from deep wells in Denmark were analysed for U, Th and K by laboratory gamma-ray analysis. Contamination of the samples by drilling mud additives, mud solids and fall down was studied by means of a wash down experiment and by comparison with the total gamma-ray response from wireline logging. It is concluded that the inorganic geochemistry on bulk cutting samples must be applied with great caution. The data are useful for geochemical characterization of well sections and for regional geochemical correlation. Radioelement abundance logs and radioelement ratio logs are presented from 3 wells in the Danish Subbasin and 2 wells in the North German Basin. The radioelement geochemistry is discussed for the successive lithostratigraphical units and a reference radioelement profile is established for the central part of the Danish Subbasin. Finally, a model describing the relationship between common lithofacies and their U content and Th/U ratio is suggested. The model deliniates the depositional environment and the relative distances to the provenance areas. It is concluded that: (1) Uranium is mobile during deposition, but since then it is fixed by stable mineral phases at depth; (2) Thorium reflects source area characteristics and that any available ions are readily adsorbed by clay minerals. Thorium anomalies may thus serve as lithostratigraphical markers; (3) Potassium occurs in unstable rock forming mineral phases. The present distribution is controlled not only by the clastic mineral assemblage, but also by the diagenetic processes through geologic time

Structural, Geochemical, and Isotopic Studies on Magmatic Dyke Swarms of the South Shetland Islands Volcanic Arc, West Antarctica - Revealing the Geodynamic History

Science.gov (United States)

Kraus, S.; Miller, H.

2003-12-01

Between 2000 and 2002 areas of up to 100,000 m2 have been mapped at several locations of the South Shetland Islands, mainly on King George and Livingston Islands. A structural analysis of the dykes and the host rocks was undertaken, and about 250 dykes were sampled for geochemical studies. On Livingston Island six different strike directions were identified, yielding a reliable relative time sequence as deduced from field-relationships. Geochemically, these dykes can be separated into five different groups, correlating with the different strike directions, one of those groups comprising two directions. Analysis of the structural data shows, that at least on Livingston Island only minor changes of the tensional situation occurred. Geochemical data reveal that all dykes of the South Shetland Islands belong to a calc-alkaline, arc-related suite, ranging from primitive basalts to highly differentiated rhyolites. Interpretation of Sr isotopic data of the dykes proves difficult, as there are indications for sea-water induced Sr-alteration. Nd isotopic analysis yield better results, revealing a three-stage development from the oldest dykes (ɛ Nd -0.2 to 0.6) on Livingston Island towards a second, younger group (ɛ Nd 2.8 to 4.2, also Livingston), terminating with a third one (ɛ Nd 5.2 to 7.6), which includes the youngest dykes on Livingston and all dykes on King George and also Penguin Island. Either two mantle sources were involved, or the amount of crustal contamination changed considerately with time. It may have been high during initial arc volcanism, because of a still unstretched crust, then decreasing continually with progressing volcanism. In any case, the pattern reflects a chronological sequence corresponding with other authors' hypothesis of a migrating arc volcanism from SW to NE, i.e. from Livingston (older dykes) towards King George Island (younger dykes). Pb isotopic data, plottet together with MORB- and sediment-samples dredged from the Drake Passage

Impact assessment of artificial recharge and geo-chemical characterization of the waters of the slick Tebolba (Eastern Tunisia)

International Nuclear Information System (INIS)

Ferchichi, Hajer

2007-01-01

This study concerned the impact assessment of artificial recharge of a coastal aquifer (Tebolba) from the waters of the dam Nebhana and chemical characterization of its waters. The analysis maps piezometric drawn and salinity at various dates since 1940, the establishment of chronic recharge from the years 1992 to 2006, as well as geochemical study of groundwater in the slick Tebolba have enabled us to reach the many results. This study using a multidisciplinary approach (hydrodynamics and geochemical) seeks an assessment of impacts of recharging the water table in Tebolba from the waters of the dam Nebhana through the history of the qualitative and quantitative water the water and a hydro-geochemical study the current state of the waters of the water. (Author). 45 refs

Regional geochemical maps of uranium in Northern Scotland. Environmental and economic considerations

International Nuclear Information System (INIS)

Plant, J.

1978-01-01

The Institute of Geological Studies geochemical mapping programme is outlined. The natural levels of uranium in rocks, soils and waters are discussed. Some practical details of geochemical mapping are given. Applications of geochemical maps of uranium in Scotland are considered: economic applications and medical geography and agriculture. A list of 38 references is appended. (U.K.)

Uranium geochemical exploration in northwestern Luzon

International Nuclear Information System (INIS)

Santos, G. Jr.; Fernandez, L.; Ogena, M.; Tauli, G.

1980-01-01

A reconnaissance geochemical stream water and sediment survey which was conducted in northwestern Luzon was able to detect ten (10) uranium anomalous areas. These anomalous areas are located along a north-south trending zone of Miocene marine clastics and sedimentary rocks with tuffaceous sediment intercalations. In general, northwest Luzon has low radioactivity except for two anomalous areas which have 3 to 6 times background radioactivity. Radon anomalies occur in sparsely scattered locations. The anomalous zones appear to be related to major north-south faults and secondary northeast-southwest trending structures. Geochemical correlations between uranium and other elements such as copper, lead, zinc, manganese, silver, cobalt and nickel are generally very poor. (author)

Seeps and springs sampling and analysis plan for the environmental monitoring plan for Waste Area Grouping 6 at Oak Ridge National Laboratory, Oak Ridge, Tennessee

Energy Technology Data Exchange (ETDEWEB)

1994-08-01

This Sampling and Analysis Plan addresses the monitoring, sampling, and analysis activities that will be conducted at seeps and springs and at two french drain outlets in support of the Environmental Monitoring Plan for Waste Area Grouping (WAG) 6. WAG 6 is a shallow-land-burial disposal facility for low-level radioactive waste at Oak Ridge National Laboratory, a research facility owned by the US Department of Energy and operated by Martin Marietta Energy Systems, Inc. Initially, sampling will be conducted at as many as 15 locations within WAG 6 (as many as 13 seeps and 2 french drain outlets). After evaluating the results obtained and reviewing the observations made by field personnel during the first round of sampling, several seeps and springs will be chosen as permanent monitoring points, together with the two french drain outlets. Baseline sampling of these points will then be conducted quarterly for 1 year (i.e., four rounds of sampling after the initial round). The samples will be analyzed for various geochemical, organic, inorganic, and radiological parameters. Permanent sampling points having suitable flow rates and conditions may be outfitted with automatic flow-monitoring equipment. The results of the sampling and flow-monitoring efforts will help to quantify flux moving across the ungauged perimeter of the site and will help to identify changes in releases from the contaminant sources.

Seeps and springs sampling and analysis plan for the environmental monitoring plan for Waste Area Grouping 6 at Oak Ridge National Laboratory, Oak Ridge, Tennessee

International Nuclear Information System (INIS)

1994-08-01

This Sampling and Analysis Plan addresses the monitoring, sampling, and analysis activities that will be conducted at seeps and springs and at two french drain outlets in support of the Environmental Monitoring Plan for Waste Area Grouping (WAG) 6. WAG 6 is a shallow-land-burial disposal facility for low-level radioactive waste at Oak Ridge National Laboratory, a research facility owned by the US Department of Energy and operated by Martin Marietta Energy Systems, Inc. Initially, sampling will be conducted at as many as 15 locations within WAG 6 (as many as 13 seeps and 2 french drain outlets). After evaluating the results obtained and reviewing the observations made by field personnel during the first round of sampling, several seeps and springs will be chosen as permanent monitoring points, together with the two french drain outlets. Baseline sampling of these points will then be conducted quarterly for 1 year (i.e., four rounds of sampling after the initial round). The samples will be analyzed for various geochemical, organic, inorganic, and radiological parameters. Permanent sampling points having suitable flow rates and conditions may be outfitted with automatic flow-monitoring equipment. The results of the sampling and flow-monitoring efforts will help to quantify flux moving across the ungauged perimeter of the site and will help to identify changes in releases from the contaminant sources

Geochemical exploration for uranium

International Nuclear Information System (INIS)

Rose, A.W.

1977-01-01

The processes and types of dispersion that produce anomalies in stream water, stream sediment, and ground water, and the factors that must be considered in planning and interpreting geochemical surveys are reviewed. Examples of surveys near known deposits show the types of results to be expected. Background values depend mainly on the content of U in rocks of the drainage area. In igneous rocks, U tends to increase with potassium from ultramafic rocks (0.01 ppM) to granitic rocks (1 to 5 ppM). Some alkalic rocks have unusually high contents of U (15 to 100 ppM). Uranium-rich provinces marked by igneous rocks unusually rich in U are recognized in several areas and appear to have a deep crustal or mantle origin. In western U.S., many tertiary tuffaceous rocks have a high U content. Sandstones, limestones, and many shales approximate the crustal abundance at 0.5 to 4 ppM, but black shales, phosphates, and some organic materials are notably enriched in U. Uranium is very soluble in most oxidizing waters at the earth's surface, but is precipitated by reducing agents (organic matter, H 2 S) and adsorbed by organic material and some Fe oxides. In most surface and ground waters, U correlates approximately with the total dissolved solids, conductivity, and bicarbonate concentration of the water, and with the U content of rocks it comes into contact with. Most surveys of stream water near known districts show distinct anomalies extending a few km to tens of km downstream. A complication with water is the large variability with time, up to x 50, as a result of changes in the ratio of ground water to direct runoff, and changes in rate of oxidation and leaching. Collection and analysis of water samples also pose some difficulties

The Use of Univariate and Multivariate Analyses in the Geochemical Exploration, Ravanj Lead Mine, Delijan, Iran

Directory of Open Access Journals (Sweden)

Mostafa Nejadhadad

2017-11-01

Full Text Available A geochemical exploration program was applied to recognize the anomalous geochemical haloes at the Ravanj lead mine, Delijan, Iran. Sampling of unweathered rocks were undertaken across rock exposures on a 10 × 10 meter grid (n = 302 as well as the accessible parts of underground mine A (n = 42. First, the threshold values of all elements were determined using the cut-off values used in the exploratory data analysis (EDA method. Then, for further studies, elements with lognormal distributions (Pb, Zn, Ag, As, Cd, Co, Cu, Sb, S, Sr, Th, Ba, Bi, Fe, Ni and Mn were selected. Robustness against outliers is achieved by application of central log ratio transformation to address the closure problems with compositional data prior to principle components analysis (PCA. Results of these analyses show that, in the Ravanj deposit, Pb mineralization is characterized by a Pb-Ba-Ag-Sb ± Zn ± Cd association. The supra-mineralization haloes are characterized by barite and tetrahedrite in a Ba- Th- Ag- Cu- Sb- As- Sr association and sub-mineralization haloes are comprised of pyrite and tetrahedrite, probably reflecting a Fe-Cu-As-Bi-Ni-Co-Mo-Mn association. Using univariate and multivariate geostatistical analyses (e.g., EDA and robust PCA, four anomalies were detected and mapped in Block A of the Ravanj deposit. Anomalies 1 and 2 are around the ancient orebodies. Anomaly 3 is located in a thin bedded limestone-shale intercalation unit that does not show significant mineralization. Drilling of the fourth anomaly suggested a low grade, non-economic Pb mineralization.

Distribution of cadmium among geochemical fractions in floodplain soils of progressing development

International Nuclear Information System (INIS)

Lair, G.J.; Graf, M.; Zehetner, F.; Gerzabek, M.H.

2008-01-01

Initial soil development in river floodplains influences soil properties and processes. In this study, suites of young floodplain soils sampled at three European rivers (Danube/Austria, Ebro/Spain and Elbe/Germany) were used to link soil development to the soils' retention capacity for cadmium. Geochemichal fractionation of original and metal-spiked soils was conducted. Cadmium remained in weakly bound fractions in both original and spiked soils, representing an entirely different behaviour than observed for copper in an earlier study. The tendency of incorporation into more stable forms over time was only slightly expressed. Correlation analysis revealed the involvement of different sorption surfaces in soil, with no single soil constituent determining cadmium retention behaviour. Nevertheless, in the calcareous soils of the Danube floodplain, we found increased cadmium retention and decreased portions of desorbable cadmium with progressing soil development. - Distribution of cadmium among geochemical fractions in floodplain soils reveals high mobility but increased retention capacity with increasing soil age and development

Uruguay mining inventory. Geochemical prospecting results of the Las Flores aerial map

International Nuclear Information System (INIS)

Zeegers, H.; Bonnefoy, D.; Garau, M.; Spangenberg, J.

1981-01-01

In the context of the Uruguay mining inventory, the aerial photography map Las Flores had been covered by a specific strategic which included geochemical prospecting elements. The surface covered has the 550 km2, and 1042 samples which they have been analized in Orleans France. 22 elements by plasma spectroscopy and gold by atomic absorption and for uranium laser spectroscopy . They have been evidenced the following anomalies: gold, Pb, Pb-Ba-Cu, Ba and Ni-Cr

Computer analysis to the geochemical of soil and stream sediments data in an area of Southern Uruguay

International Nuclear Information System (INIS)

Spangenberg, J.

2012-01-01

This work is about geochemical interpretation of multi-element data from a soil and stream sediment survey carried out in Southern of Uruguay .This zone has several occurrences of metal sulphide mineralization

Regional geochemical baselines for Portuguese shelf sediments

International Nuclear Information System (INIS)

Mil-Homens, M.; Stevens, R.L.; Cato, I.; Abrantes, F.

2007-01-01

Metal concentrations (Al, Cr, Cu, Ni, Pb and Zn) from the DGM-INETI archive data set have been examined for sediments collected during the 1970s from 267 sites on the Portuguese shelf. Due to the differences in the oceanographic and sedimentological settings between western and Algarve coasts, the archive data set is split in two segments. For both shelf segments, regional geochemical baselines (RGB) are defined using aluminium as a reference element. Seabed samples recovered in 2002 from four distinct areas of the Portuguese shelf are superimposed on these models to identify and compare possible metal enrichments relative to the natural distribution. Metal enrichments associated with anthropogenic influences are identified in three samples collected nearby the Tejo River and are characterised by the highest enrichment factors (EF; EF Pb Zn < 4). EF values close to 1 suggest a largely natural origin for metal distributions in sediments from the other areas included in the study. - Background metal concentrations and their natural variability must be established before assessing anthropogenic impacts

Organic geochemical investigation and coal-bed methane characteristics of the Guasare coals (Paso Diablo mine, western Venezuela)

Science.gov (United States)

Quintero, K.; Martinez, M.; Hackley, P.; Marquez, G.; Garban, G.; Esteves, I.; Escobar, M.

2011-01-01

The aim of this work was to carry out a geochemical study of channel samples collected from six coal beds in the Marcelina Formation (Zulia State, western Venezuela) and to determine experimentally the gas content of the coals from the Paso Diablo mine. Organic geochemical analyses by gas chromatography-mass spectrometry and isotopic analyses on-line in coalbed gas samples were performed. The results suggest that the Guasare coals were deposited in a continental environment under highly dysoxic and low salinity conditions. The non-detection of 18??(H)-oleanane does not preclude that the organic facies that gave rise to the coals were dominated by angiosperms. In addition, the presence of the sesquiterpenoid cadalene may indicate the subordinate contribution of gymnosperms (conifers) in the Paleocene Guasare mire. The average coalbed gas content obtained was 0.6 cm3/g. ??13C and D values indicate that thermogenic gas is prevalent in the studied coals. Copyright ?? Taylor & Francis Group, LLC.

A review of single-sample-based models and other approaches for radiocarbon dating of dissolved inorganic carbon in groundwater

Science.gov (United States)

Han, L. F; Plummer, Niel

2016-01-01

underlying assumptions on which the various models and approaches are based can result in a wide range of estimates of 14C0 and limit the usefulness of radiocarbon as a dating tool for groundwater. In each of the three generalized approaches (single-sample-based models, statistical approach, and geochemical mass-balance approach), successful application depends on scrutiny of the isotopic (14C and 13C) and chemical data to conceptualize the reactions and processes that affect the 14C content of DIC in aquifers. The recently developed graphical analysis method is shown to aid in determining which approach is most appropriate for the isotopic and chemical data from a groundwater system.

Geochemical site-selection criteria for HLW repositories in Europe and North America

International Nuclear Information System (INIS)

Savage, David; Arthur, Randolph C.; Sasamoto, Hiroshi; Shibata, Masahiro; Yui, Mikazu

2000-01-01

Geochemical as well as socio-economic issues associated with the selection of potential sites to host a high-level nuclear waste repository have received considerable attention in repository programs in Europe (Belgium, Finland, France, Germany, Spain, Sweden, Switzerland and the U.K.) and North America (Canada and the United States). The objective of the present study is to summarize this international experience with particular emphasis on geochemical properties that factor into the adopted site-selection strategies. Results indicate that the geochemical properties of a site play a subordinate role, at best, to other geotechnical properties in the international site-selection approaches. In countries where geochemical properties are acknowledged in the site-selection approach, requirements are stated qualitatively and tend to focus on associated impacts on the stability of the engineered barrier system and on radionuclide transport. Site geochemical properties that are likely to control the long-term stability of geochemical conditions and radionuclide migration behavior are unspecified, however. This non-prescriptive approach may be reasonable for purposes of screening among potential sites, but a better understanding of site properties that are most important in controlling the long-term geochemical evolution of the site over a range of possible scenarios would enable the potential sites to be ranked in terms of their suitability to host a repository. (author)

Some results of processing NURE geochemical sampling in the northern Rocky Mountain area

International Nuclear Information System (INIS)

Thayer, P.A.; Cook, J.R.; Price, V. Jr.

1980-01-01

The National Uranium Resource Evaluation (NURE) program was begun in the spring of 1973 to evaluate domestic uranium resources in the continental United States and to identify areas favorable for uranium exploration. The significance of the distribution of uranium in natural waters and sediments will be assessed as an indicator of favorable areas for the discovery of uranium deposits. This paper is oriented primarily to the discussion of stream sediments. Data for the Challis 1 0 x 2 0 NTMS quadrangle will be used for specific samples of NURE data processing. A high-capacity neutron activation analysis facility at SRL is used to determine uranium and about 19 other elements in hydrogeochemical samples. Evaluation of the areal distributions of uranium ratios demonstrate that most of the high U/Hf, U/Th and U/(Th + Hf) ratios occur scattered throughout the western two-thirds of the quadrangle. Most of the higher ratio values are found in samples taken at sites underlain by granitic rocks of the Idaho batholith or Tertiary-age plutons

Granite-repository - geochemical environment

International Nuclear Information System (INIS)

1979-04-01

Some geochemical data of importance for a radioactive waste repository in hard rock are reviewed. The ground water composition at depth is assessed. The ground water chemistry in the vicinity of uranium ores is discussed. The redox system in Swedish bedrock is described. Influences of extreme climatic changes and of repository mining and construction are also evaluated

Geochemical signature of columbite-tantalite and radiometric survey of radioactive pegmatites in the region of Parelhas, Rio Grande do Norte, Brazil

International Nuclear Information System (INIS)

Moura, Jorge Costa de

2013-01-01

This thesis is the result of geochemical, structural and radiometric investigations on radioactive pegmatites of the Borborema Pegmatitic Province in Northeast Brazil. The studied area, located in the surroundings of the city of Parelhas in the region of the Serra da Borborema, is well known for its thousands of pegmatitic bodies exploited in primitive mines called 'garimpos'. The main goal was to find an efficient, cheap and routine inspection procedure to identify the origin of commercialized radioactive columbite-tantalite (coltan) ore. The Brazilian Nuclear Energy Agency (CNEN) controls uranium commerce and nuclear activity in Brazil. Without an effective method to characterize coltan ores from different localities it is impossible to control the trade. The here presented new method was developed by correlating structural features of these pegmatites with the geochemical behavior of their coltan samples. It was found that the variation of the ratio U/Th versus Nb 2 O 5 /Ta 2 O 5 provides geochemical signatures (analytical fingerprints) for the source location of such ore. A test of the new method with coltan samples of commercial batches from the Brazilian states Amapa and Rondonia also generated distinct geochemical signatures. A radiometric survey (CPS) was carried out in several mines and pegmatites to study the environmental impact of gamma radiation. It included in situ measurements of pegmatite walls, host rocks, soil, and accumulated water and revealed that gamma emitters are hardly solubilized and environmental gamma radiation therefore generally is not enhanced to a dangerous level. (author)

Detailed geochemical survey for east-central Minnesota, geology and geochemistry of selected uranium targets

International Nuclear Information System (INIS)

Morey, G.B.; Lively, R.S.

1980-01-01

Results of a detailed geochemical survey of approximately 6820 km 2 in parts of Aitkin, Carlton, Kanabec, and Pine Counties, east-central Minnesota are reported. Geochemical data are presented for 883 groundwater samples and 200 bedrock samples. Although all of the groundwaters in the study area have similar major-element concentrations and therefore presumably a common ancestry, small differences in the minor-element concentrations serve to characterize various aquifers, both in the Quaternary deposits and in the bedrock. All of the aquifers locally yield waters having statistically anomalous concentrations of uranium or radon, but these anomalies are spatially coincident only in a few places and particularly in three geologic environments considered favorable for uranium mineralization. These include the following: (1) Thomson Formation near the unconformably overlying Fond du Lac Formation, (2) Hinckley Sandstone near a major fault system, and (3) Denham Formation near the unconformity with the McGrath Gneiss, particularly where these rocks are faulted and overlain by the Fond du Lac Formation. One additional uranium environment characterized by thin laminae of uraniferous apatite was located in the Thomson Formation during outcrop reconnaissance and sampling. The coincidence of this and other anomalously high uranium values in the bedrock with specific uranium and radon anomalies in the groundwater confirms the usefulness of the hydrogeochemical data to uranium exploration in this glaciated terrane

Mineralogical, geochemical and radiological characterisation of Selmo Formation in Batman area, Turkey.

Science.gov (United States)

Isik, Umit; Damla, Nevzat; Akkoca, Dicle Bal; Cevik, Uğur

2012-06-01

This work deals with the mineralogical, geochemical and radiological characterisations of Selmo Formation in Batman neighbourhood. The upper Miocene-Pliocene Selmo Formation is common in the centre of Batman and composed of carbonated sandy claystones and silty-sandy stone lenses. The common whole minerals of the samples are quartz, feldspars, calcite and dolomite. The clay minerals are smectite, illite, chlorite and mixed-layer clay (chlorite-smectite). The geochemical mean values of the samples are 51.7% SiO(2); 12.6% Al(2)O(3); 6.2% Fe(2)O(3); 3.6% MgO; 6.3% CaO; 1.1% Na(2)O; 1.7% K(2)O; 0.8% TiO(2); 0.2% P(2)O(5); 0.1% MnO; and 0.03% Cr(2)O(3). In addition, baseline maps for the concentrations of each radionuclide, the radium equivalent activity and the outdoor gamma dose rate distributions have been plotted for the study area. The mean activity concentrations of (226)Ra, (232)Th, (40)K and (137)Cs were determined to be 32, 24, 210 and 9 Bq kg(-1), respectively. The assessments of the radiological hazard indices, such as radium equivalent activity, absorbed dose rate in air, annual effective dose equivalent, excess lifetime cancer risk, external hazard index and internal hazard index, were calculated and compared with the internationally accepted reference values. This study shows that the concentrations of radioactivities in the measured samples were within the recommended safety limits and did not pose to be any significant source of radiation hazard.

Expected Geochemical and Mineralogical Properties of Meteorites from Mercury: Inferences from Messenger Data

Science.gov (United States)

McCubbin, F. M.; McCoy, T. J.

2016-01-01

Meteorites from the Moon, Mars, and many types of asteroid bodies have been identified among our global inventory of meteorites, however samples of Mercury and Venus have not been identified. The absence of mercurian and venusian meteorites could be attributed to an inability to recognize them in our collections due to a paucity of geochemical information for Venus and Mercury. In the case of mercurian meteorites, this possibility is further supported by dynamical calculations that suggest mercurian meteorites should be present on Earth at a factor of 2-3 less than meteorites from Mars [1]. In the present study, we focus on the putative mineralogy of mercurian meteorites using data obtained from the MErcury Surface, Space ENvironment, GEochemistry, and Ranging (MESSENGER) spacecraft, which has provided us with our first quantitative constraints on the geochemistry of planet Mercury. We have used the MESSENGER data to compile a list of mineralogical and geochemical characteristics that a meteorite from Mercury is likely to exhibit.

The relation between geochemical characteristics and landslide in Hungtsaiping area, Nantou, Taiwan

Science.gov (United States)

Lin, P.; Tsai, L.

2009-12-01

Hungtsaiping is located at the south bank of the Yonglu stream, Chungliao Village of Nantou County, central Taiwan. Hungtsaiping landslide was triggered by the Chi-Chi earthquake (Mw=7.6) occurring on September 20, 1999 UTC near the town of Chi-Chi in Nantou County, central Taiwan. Coping with the geological and geomorphologic investigations, this study makes an attempt to find the relation between geochemical characteristics and landslide in Hungtsaiping area. Water samples were collected from spring waters, creeks, ponds, groundwater and the Yonglu stream once every month from May 2008 to May 2009. Oxygen and hydrogen stable isotopic, ionic concentrations, as well as electrical conductivity and pH value were analyzed. The results indicate that calcium and magnesium bicarbonate-rich water was found on the top and the middle part of the slope. On the other hand, sodium bicarbonate-rich water as well as exceptionally high sulfate concentration was found on the foot of the slope, the sulfate content decreased with increasing elevations until the middle part of slope. A conceptual model of flow process and water origin in Hungtsaiping landslide was established by summarizing the features of hydrogeochemical analyses and the profiles in this study. Keywords: landslide, geochemical characteristics, isotope, hydrochemistry. Fig. 1 The sampling locations of Hungtsaiping landslide. Fig. 2 Isogram: the concentration of sulfate in May 2008 in Hungtsaiping area.

Final Sampling and Analysis Plan for Background Sampling, Fort Sheridan, Illinois

National Research Council Canada - National Science Library

1995-01-01

.... This Background Sampling and Analysis Plan (BSAP) is designed to address this issue through the collection of additional background samples at Fort Sheridan to support the statistical analysis and the Baseline Risk Assessment (BRA...

A Low-Li Geochemical Province in the NE Atlantic

DEFF Research Database (Denmark)

Bailey, J. C.; Gwozdz, R.

1978-01-01

Lithium was analysed in 392 basalts and related igneous rocks from the North Atlantic Tertiary-Recent province using activation analysis and Čerenkov counting. Monotonous Li values of 5.5±2 ppm in NE Atlantic basalts define a low-Li geochemical province which has persisted for 60 million years...... basalt series. No whole-rock coherence is observed between Li and Mg, K, Rb or Ca. Mantle phlogopite is considered to play an insignificant rôle in controlling the Li levels of NE Atlantic basalts....

Geochemical effects of CO2 sequestration in sandstones under simulated in situ conditions of deep saline aquifers

International Nuclear Information System (INIS)

Wigand, M.; Carey, J.W.; Schuett, H.; Spangenberg, E.; Erzinger, J.

2008-01-01

The geochemical effects of brine and supercritical CO 2 (SCCO 2 ) on reservoir rocks from deep (1500-2000 m) saline aquifers were examined via experimental simulation at in situ conditions. Dry sandstone samples were mounted in a triaxial cell and autoclave system, evacuated, and saturated with 1 M NaCl solution. The brine-rock system was allowed to react at 30 MPa confining pressure, 15 MPa pore fluid pressure, and 60 deg. C while SCCO 2 was injected at a pressure gradient of 1-2 MPa. The experiment was conducted for a period of 1496 h, during which fluids were periodically sampled and analyzed. The pH measured in partially degassed fluid samples at 25 deg. C decreased from a starting value of 7.0-4.3 (9 days) and finally 5.1 after saturation with SCCO 2 . Fluid analyses indicate that most of the major (e.g. Ca, Mg, Fe, Mn) and trace elements (e.g. Sr, Ba, Pb) of the sandstone increase in concentration during the reaction with brine and SCCO 2 . These results are supported by scanning electron microscopy which indicates dissolution of dolomite cement, K-feldspar, and albite. In addition to dissolution reactions the formation of montmorillonite was observed. By adjusting surface area and reaction rates of dissolution and precipitation, geochemical modeling of the experiments could reproduce long-term trends in solution chemistry and indicated limited rates of dissolution as the system remained strongly undersaturated with most minerals, including carbonates. The geochemical models could not account for decreases in concentration of some elements, changes in solution composition resulting from changes in imposed pressure gradient, and the observed Ca/Mg and Si/Al ratios in solution

Application of the PHREEQC geochemical computer model during the design and operation of UK mine water treatment schemes

Energy Technology Data Exchange (ETDEWEB)

Croxford, S.J.; England, A.; Jarvis, A.P. [IMC White Young Green Engineering and Environment, Sutton-in-Ashfield (United Kingdom)

2004-07-01

The UK Coal Authority operates more than 20 full-scale mine water treatment schemes. The PHREEQC geochemical model has been used during the design and operation of two of the UK Coal Authority's treatment systems to assess whether it is possible to more accurately predict the fate and behaviour of contaminants through the treatment process. These systems are at Frances Colliery, Fife, Scotland, and at Horden Colliery, County Durham, England. The characteristics of the mine water at these sites, and the treatment systems installed to remediate them, are described. At Frances Colliery the following issues have been investigated using the PHREEQC model: determination of optimum alkali dose rate; and investment of secondary mineralization that causes pipe fouling. At Horden Colliery areas investigated using the PHREEQC model are: prediction of sludge volume production for various alkali reagents; predication of the influence of elevated carbon dioxide partial pressures on alkali requirements; and influence of elevated chloride concentration on sludge characteristics and production. The results of the investigation are presented and discussed. The study suggests that geochemical modelling may be a useful tool in determining both the geochemical processes occurring within a mine water treatment system and ultimately the likely costs involved during the operation of a particular scheme. Plans for future work include further validation of the PHREEQC model predictions by careful sampling and analysis of water chemistry and secondary mineral phases through the treatment systems. In the future it is hoped that the PHREEQC model may become a useful tool in the design phase of mine water treatment systems. 7 refs., 8 tabs.

Geochemical Distribution of Lead and Chromium in River Getsi-Kano

African Journals Online (AJOL)

Geochemical forms of lead (Pb) and Chromium (Cr) from the sediment of River Getsi Kano-Nigeria were determined using Atomic Absorption spectrometer for eighteen months. Apart from determination of the metals in water, geochemical forms of the metals were also evaluated into five fractions. Exchangeable, bound to ...

On a possible parent crater for Australasian tektites: Geochemical, isotopic, geographical and other constraints

Czech Academy of Sciences Publication Activity Database

Mizera, Jiří; Řanda, Zdeněk; Kameník, Jan

2016-01-01

Roč. 154, MAR (2016), s. 123-137 ISSN 0012-8252 R&D Projects: GA ČR GA13-22351S; GA MŠk(CZ) LM2011019 Institutional support: RVO:67985891 ; RVO:61389005 Keywords : Australasian tektite * Parent crater * Geochemical analysis * Isotope analysis * Chinese loess * Badain Jaran Subject RIV: BG - Nuclear, Atomic and Molecular Physics, Colliders; DD - Geochemistry (USMH-B) Impact factor: 7.051, year: 2016

The flotation tailings of the former Pb-Zn mine of Touiref (NW Tunisia): mineralogy, mine drainage prediction, base-metal speciation assessment and geochemical modeling.

Science.gov (United States)

Othmani, Mohamed Ali; Souissi, Fouad; Bouzahzah, Hassan; Bussière, Bruno; da Silva, Eduardo Ferreira; Benzaazoua, Mostafa

2015-02-01

The underground extraction of Pb-Zn mineralization in the Touiref area stopped in 1958. A large volume of flotation tailings (more than 500 Mt) containing sulfides were deposited in a tailings impoundment. The goals of this study are to evaluate the neutralization capacity of the unoxidized and oxidized tailings, to assess the speciation of metals between the different components of the tailings material, and to assess the mobility of metals and the secondary minerals' precipitation in pore waters using geochemical modeling. To accomplish these objectives, representative samples from both fresh and oxidized zones were collected along a vertical profile through the tailings pile. Physical, chemical (ICP-MS), and mineralogical characterization (X-ray diffraction (XRD), reflected light microscopy, scanning electron microscope (SEM)) of these samples was performed. Grain size analysis shows that the tailings are dominated by silt- to sand-sized fractions. The microscopic observation highlights the presence of pyrite, marcasite, galena, and sphalerite as primary minerals in a carbonated matrix. The study reveals also the presence of secondary minerals represented by cerussite, smithsonite, anglesite, and Fe oxi-hydroxides as important scavengers for trace elements. The static tests show that the presence of calcite in the tailing samples ensures acid-neutralizing capacity (ANC), which is significantly greater than the acidity potential (PA). The geochemical characterization of the unoxidized samples shows higher Cd, Pb, and Zn concentrations than the oxidized samples containing the highest values for Fe and SO4. Sequential extraction tests show that significant percentages of metals are distributed between the acid-soluble fractions (Cd, Pb, and Zn) and the reducible one (Zn). Pore water analysis indicates that Ca is the dominant cation (8,170 and 6,200 mg L(-1), respectively), whereas sulfate is the principal anion (6,900 and 5,100 mg L(-1), respectively). Saturation

A Geochemical Comparison of the Northern Peninsular Ranges Batholith in Southern California and the Coastal Batholith in Southern Peru

Science.gov (United States)

Clausen, B. L.; Martínez Ardila, A. M.; Morton, D. M.

2010-12-01

An extensive geochemical data set from the northern Peninsular Ranges Batholith (PRB) in southern California is compared and contrasted with the Arequipa segment of the Peruvian Coastal Batholith, including new granitoid samples recently collected near Ica (14°S, 76°W). The data include major and trace elements and Sr isotope ratios. This is part of an on-going study of subduction-related magmatism to refine a petrogenetic model of crust formation at plate boundaries, with a particular interest in the role of magma mixing. Research in the northern PRB suggests that continental crust is formed in several cycles: (1) mantle melting to give mafic volcanics and gabbroic intrusives, (2) basalt/gabbro melting to give felsic granitoids uncontaminated by continental crust and having low initial 87Sr/86Sr (Sri) values less than 0.704, and (3) crustal melting to give high Sri values greater than 0.704. Geochemical evidence was used to determine the extent of mixing between mafic and felsic magma that produced rocks of intermediate SiO2 composition. These differentiation cycles formed a west to east chronologic sequence and yielded granitoids of gabbro, tonalite, and granodiorite composition. Using principal component analysis on the northern PRB granitoids, the four factors affecting geochemical composition were categorized as differentiation, crustal contamination, depth of magma source, and conditions that yield a range from calcic to more alkaline granitoids. A similar major and trace element analysis is being done for a classic result of subduction in the Peruvian Coastal Batholith. The Peruvian samples recently collected include granitoids of the upper Cretaceous Coastal Batholith, as well as the associated volcanics of Cretaceous and Jurassic age. The Coastal Batholith samples include a range of granitoids from the early gabbros and from the four batholithic super-units (from west to east: Linga, Pampahuasi, Tiabaya, and Incahuasi) containing a combination of diorite

Investigation of the geochemical evolution of groundwater under agricultural land: A case study in northeastern Mexico

Science.gov (United States)

Ledesma-Ruiz, Rogelio; Pastén-Zapata, Ernesto; Parra, Roberto; Harter, Thomas; Mahlknecht, Jürgen

2015-02-01

Zona Citrícola is an important area for Mexico due to its citriculture activity. Situated in a sub-humid to humid climate adjacent to the Sierra Madre Oriental, this valley hosts an aquifer system that represents sequences of shales, marls, conglomerates, and alluvial deposits. Groundwater flows from mountainous recharge areas to the basin-fill deposits and provides base flows to supply drinking water to the adjacent metropolitan area of Monterrey. Recent studies examining the groundwater quality of the study area urge the mitigation of groundwater pollution. The objective of this study was to characterize the physical and chemical properties of the groundwater and to assess the processes controlling the groundwater's chemistry. Correlation was used to identify associations among various geochemical constituents. Factor analysis was applied to identify the water's chemical characteristics that were responsible for generating most of the variability within the dataset. Hierarchical cluster analysis was employed in combination with a post-hoc analysis of variance to partition the water samples into hydrochemical water groups: recharge waters (Ca-HCO3), transition zone waters (Ca-HCO3-SO4 to Ca-SO4-HCO3) and discharge waters (Ca-SO4). Inverse geochemical models of these groups were developed and constrained using PHREEQC to elucidate the chemical reactions controlling the water's chemistry between an initial (recharge) and final water. The primary reactions contributing to salinity were the following: (1) water-rock interactions, including the weathering of evaporitic rocks and dedolomitization; (2) dissolution of soil gas carbon dioxide; and (3) input from animal/human wastewater and manure in combination with by denitrification processes. Contributions from silicate weathering to salinity ranged from less important to insignificant. The findings suggest that it may not be cost-effective to regulate manure application to mitigate groundwater pollution.

The potential of mid- and near-infrared diffuse reflectance spectroscopy for determining major- and trace-element concentrations in soils from a geochemical survey of North America

Science.gov (United States)

Reeves, J. B.; Smith, D.B.

2009-01-01

In 2004, soils were collected at 220 sites along two transects across the USA and Canada as a pilot study for a planned soil geochemical survey of North America (North American Soil Geochemical Landscapes Project). The objective of the current study was to examine the potential of diffuse reflectance (DR) Fourier Transform (FT) mid-infrared (mid-IR) and near-infrared (NIRS) spectroscopy to reduce the need for conventional analysis for the determination of major and trace elements in such continental-scale surveys. Soil samples (n = 720) were collected from two transects (east-west across the USA, and north-south from Manitoba, Canada to El Paso, Texas (USA), n = 453 and 267, respectively). The samples came from 19 USA states and the province of Manitoba in Canada. They represented 31 types of land use (e.g., national forest, rangeland, etc.), and 123 different land covers (e.g., soybeans, oak forest, etc.). The samples represented a combination of depth-based sampling (0-5 cm) and horizon-based sampling (O, A and C horizons) with 123 different depths identified. The set was very diverse with few samples similar in land use, land cover, etc. All samples were analyzed by conventional means for the near-total concentration of 49 analytes (Ctotal, Ccarbonate and Corganic, and 46 major and trace elements). Spectra were obtained using dried, ground samples using a Digilab FTS-7000 FT spectrometer in the mid- (4000-400 cm-1) and near-infrared (10,000-4000 cm-1) at 4 cm-1 resolution (64 co-added scans per spectrum) using a Pike AutoDIFF DR autosampler. Partial least squares calibrations were develop using: (1) all samples as a calibration set; (2) samples evenly divided into calibration and validation sets based on spectral diversity; and (3) samples divided to have matching analyte concentrations in calibration and validation sets. In general, results supported the conclusion that neither mid-IR nor NIRS would be particularly useful in reducing the need for conventional

Geochemical study of evaporite and clay mineral-oxyhydroxide samples from the Waste Isolation Pilot Plant site

International Nuclear Information System (INIS)

Brookins, D.G.

1993-06-01

Samples of clay minerals, insoluble oxyhydroxides, and their host evaporites from the WIPP site have been studied for their major and minor elements abundances, x-ray diffraction characteristics, K-Ar ages, and Rb-Sr ages. This study was undertaken to determine their overall geochemical characteristics and to investigate possible interactions between evaporates and insoluble constituents. The evaporite host material is water-soluble, having Cl/Br ratios typical of marine evaporites, although the Br content is low. Insoluble material (usually a mixture of clay minerals and oxyhydroxide phases) yields very high Cl/Br ratios, possibly because of Cl from admixed halide minerals. This same material yields K/Rb and Th/U ratios in the normal range for shales; suggesting little, if any, effect of evaporite-induced remobilization of U, K, or Rb in the insoluble material. The rare-earth element (REE) data also show normal REE/chondrite (REE/CHON) distribution patterns, supporting the K/Rb and Th/U data. Clay minerals yield K-Ar dates in the range 365 to 390 Ma and a Rb-Sr isochron age of 428 ± 7 Ma. These ages are well in excess of the 220- to 230-Ma formational age of the evaporites, and confirm the detrital origin of the clays. The ages also show that any evaporite or clay mineral reactions that might have occurred at or near the time of sedimentation and diagenesis were not sufficient to reset the K-Ar and Rb-Sr systematics of the clay minerals. Further, x-ray data indicate a normal evaporitic assemblage of clay minerals and Fe-rich oxyhydroxide phases. The clay minerals and other insoluble material appear to be resistant to the destructive effects of their entrapment in the evaporites, which suggests that these insoluble materials would be good getters for any radionuclides (hypothetically) released from the storage of radioactive wastes in the area

Geochemical prospecting in Guiana

International Nuclear Information System (INIS)

Coulomb, R.

1957-01-01

During the last few years geochemical prospecting techniques have become common usage in the field of mineral deposit prospecting. The real scope of these methods lies in their use in the prospecting of large areas. The most promising use of the geochemistry and hydro-geochemistry of uranium is in heavily forested tropical territories, with few outcrops, where radiometry is strongly handicapped. (author) [fr

Geochemical and geochronological constrains on the Chiang Khong volcanic rocks (northwestern Thailand) and its tectonic implications

Science.gov (United States)

Qian, Xin; Feng, Qinglai; Chonglakmani, Chongpan; Monjai, Denchok

2013-12-01

Volcanic rocks in northwestern Thailand exposed dominantly in the Chiang Khong area, are commonly considered to be genetically linked to the tectonic evolution of the Paleo-Tethyan Ocean. The volcanic rocks consist mainly of andesitic to rhyolitic rocks and are traditionally mapped as Permian-Triassic sequences. Our zircon U-Pb geochronological results show that two andesitic samples (TL-1-B and TL-31-B), are representative of the Doi Yao volcanic zone, and give a mean weighted age of 241.2±4.6 Ma and 241.7±2.9 Ma, respectively. The rhyolitic sample (TL-32-B1) from the Doi Khun Ta Khuan volcanic zone erupted at 238.3±3.8 Ma. Such ages indicate that Chiang Khong volcanic rocks erputed during the early Middle Triassic period. Seven samples from the Doi Yao and Doi Khun Ta Khuan zones exhibit an affinity to arc volcanics. Three rhyolitic samples from the Chiang Khong area have a geochemical affinity to both arc and syn-collisional volcanic rocks. The Chiang Khong arc volcanic rocks can be geochemically compared with those in the Lampang area in northern Thailand, also consistent with those in Jinghong area of southwestern Yunnan. This indicates that the Chiang Rai arc-volcanic zone might northwardly link to the Lancangjiang volcanic zone in southwestern China.

Geochemical processes of mercury in Wujiangdu and Dongfeng reservoirs, Guizhou, China

International Nuclear Information System (INIS)

Feng Xinbin; Jiang Hongmei; Qiu Guangle; Yan Haiyu; Li Guanghui; Li Zhonggen

2009-01-01

The geochemical processes of mercury in Dongfeng (DF) and Wujiangdu (WJD) reservoirs, which were constructed in 1992 and 1979, respectively in Wujiang River, which is the upper branch of Yangtze River were investigated. One sampling site was chosen upriver of 1 km from the dam for each reservoir. Three sampling campaigns were conducted at these sampling sites in December 2003, April 2004 and July 2004, respectively. The distributions of different mercury species in the water column, sediment, and sediment pore water were studied. We found that the sediment is the net source of both inorganic and MeHg to the water column for both reservoirs. The MeHg diffusion fluxes in WJD reservoir at all sampling campaigns were significantly higher than those in DF reservoir. Our study demonstrated that the high primary productivity in the reservoir produced elevated organic matter content that would favor the methylmercury production in sediment. - Surface sediment in the reservoirs is the active mercury methylating sites in the systems.

Geochemical homogeneity of tuffs at the potential repository level, Yucca Mountain, Nevada

International Nuclear Information System (INIS)

Peterman, Zell E.; Cloke, Paul

2001-01-01

In a potential high-level radioactive waste repository at Yucca Mountain, Nevada, radioactive waste and canisters, drip shields protecting the waste from seepage and from rock falls, the backfill and invert material of crushed rock, the host rock, and water and gases contained within pores and fractures in the host rock together would form a complex system commonly referred to as the near-field geochemical environment. Materials introduced into the rock mass with the waste that are designed to prolong containment collectively are referred to as the Engineered Barrier System, and the host rock and its contained water and gases compose the natural system. The interaction of these component parts under highly perturbed conditions including temperatures well above natural ambient temperatures will need to be understood to assess the performance of the potential repository for long-term containment of nuclear waste. The geochemistry and mineralogy of the rock mass hosting the emplacement drifts must be known in order to assess the role of the natural system in the near-field environment. Emplacement drifts in a potential repository at Yucca Mountain would be constructed in the phenocryst-poor member of the Topopah Spring Tuff which is composed of both lithophysal and nonlithophysal zones. The chemical composition of the phenocryst-poor member has been characterized by numerous chemical analyses of outcrop samples and of core samples obtained by surface-based drilling. Those analyses have shown that the phenocryst-poor member of the Topopah Spring Tuff is remarkably uniform in composition both vertically and laterally. To verify this geochemical uniformity and to provide rock analyses of samples obtained directly from the potential repository block, major and trace elements were analyzed in core samples obtained from drill holes in the cross drift, which was driven to provide direct access to the rock mass where emplacement drifts would be constructed

Geochemical Study on an Abandoned Copper Smelting Plant Using Rare Earth Elements

Science.gov (United States)

Sun, S. H.

2017-12-01

The Shuei Nan Dong Copper Smelting Plant smelting is located on the northern coast of New Taipei City, Taiwan. The plant built in 1906 for but has been shut down since 1987. However, the watershed is continuing to discharge acid mine water into the sea; and, the acid mine drainage releases high amounts of sulfate, heavy metals without any treatment. In this study, the water samples were sequentially collected along the main channel and its tributaries in the watershed. The results of hydrochemical analysis show that the untreated inflow water can be characterized with low pH value of 80% of the total variance and almost all chemical components have high loadings in the PC. Therefore, the hydrochemical properties in the watershed are mainly dominated by the mixing process between main channel and the major tributary but the geochemical reactions during flow down the channel is insignificant. Rare earth elements (REE) are an excellent tracer, which can indicate sources of chemical components and geochemical reactions in water. The analysis results demonstrate two distinct REE patterns. The water with low REE can be characterized by prominent Eu positive anomaly and Ce negative anomaly, which may result from the alteration of Na-plagioclase in sandstone and oxidation reaction when contact with air, respectively. On the contrary, the water with high REE shows only minor Ce negative anomaly and insignificant Eu positive anomaly. In addition, there is an enrichment of middle REE in high-REE water, which is quite different with the REE pattern of pyrite. According to the Grawunder's study (2014), it corresponds to the complexation to sulphite during pyrite oxidation. It is worth noting that REE show no considerable fractionation along the channel and confirms the results from PCA. It can be derived that the water may not reached equilibrium condition. A simple aerated retention pool could dramatically reduce the pollutants due to coprecipitation of iron oxide and aluminum

Summary report on geochemical barrier special study

International Nuclear Information System (INIS)

1988-12-01

Long-term management of uranium mill tailings must provide assurance that soluble contaminants will not migrate beyond the Point of Compliance. Conventional management alternatives provide containment through the use of physical barriers which are designed to prevent migration of water through the tailings pile. An alternative is to geochemically modify the tailings to immobilize the contaminants. This investigation examined three potential geochemical modifiers to determine their ability to immobilize inorganic groundwater contaminants found in uranium mill tailings. These modifiers were hydrated lime (Ca(OH) 2 ), limestone (CaCO 3 ), and a sphaegnum peat moss. This investigation focused on both the geochemical interactions between the tailings and the modifiers, and the effects the modifiers had on the physical strength of the tailings. The geochemical investigations began with characterization of the tailings by X-ray diffraction and scanning electron microscopy. This was followed by batch leaching experiments in which various concentrations of each modifier were added to tailings in shaker flasks and allowed to come to equilibrium. Finally, column experiments were conducted to simulate flow through a tailings pile. The results show that all of the modifiers were at least moderately effective at immobilizing most of the groundwater contaminants of concern at uranium mill tailings sites. Hydrated lime was able to achieve 90 percent concentration reduction of arsenic, cadmium, selenium, uranium, and sulfate when added at a two percent concentration. Limestone was somewhat less effective and peat removed greater than 90 percent of arsenic, lead, uranium, and sulfate at a one percent concentration. The column tests showed that kinetic and/or mass transfer limitations are important and that sufficient time must be allowed for the immobilization reactions to occur

New results for Palaeozoic volcanic phases in the Prague Basin – magnetic and geochemical studies of Lištice, Czech Republic

Directory of Open Access Journals (Sweden)

Tiiu Elbra

2015-02-01

Full Text Available Palaeo-, rock magnetic and geochemical studies were conducted on volcanic samples from the Lištice area to improve the knowledge of Palaeozoic volcanic evolution in the Prague Basin. The magnetic data display no significant differences between two studied localities, indicating one magnetizing event for both localities. Geochemical data suggest that Lištice basalt could have originated from deep melting of the garnet peridotite mantle source during the attenuation and rifting of the continental lithosphere connected with asthenospheric mantle upwelling. The dataset furthermore supports the evidence of syn- or post-intrusive fluid interactions and low-temperature stages of alteration. The Ti-magnetite within amygdales of the samples was found to be carrying the characteristic remanent magnetization and reflects probably the Permo-Carboniferous remagnetization of volcanic phases.

Proceedings of 2. Brazilian Geochemical Congress

International Nuclear Information System (INIS)

1989-01-01

Some works about geochemistry are presented, including themes about geochemical exploration, lithogeochemistry and isotope geochemistry, environmental geochemistry, analytical geochemistry, geochemistry of carbonatites and rare earth elements and organic geochemistry. (C.G.C.) [pt

Factors of the accumulation of heavy metals and metalloids at geochemical barriers in urban soils

Science.gov (United States)

Kosheleva, N. E.; Kasimov, N. S.; Vlasov, D. V.

2015-05-01

The bulk contents and concentrations of mobile (extracted by an ammonium acetate buffer with EDTA) Cd, Pb, Sb, As, Bi, Zn, and Cu were determined in the surface horizons of urban soils in the Eastern administrative okrug of Moscow. The regression analysis showed that the accumulation of these metals and metalloids in the soils is controlled by the physicochemical soil properties and by number of anthropogenic factors and landscape conditions (geochemical position, type of loose deposits, character of land use, dust load, vehicle emissions, building pattern, percent of green areas, and the extent of sealed soils). The precipitation of studied elements on the geochemical barriers had the following regularities: Cd, Cu, and Zn accumulated on the alkaline barriers; Bi, Sb, As, Cu, Pb, and Zn, on chemisorption barriers; Sb, As, and Pb, on organomineral barriers; and Cd and Cu, on the sorption-sedimentation barriers. Technogenic transformation of the physicochemical properties of urban soils resulted in the increase of the mean bulk contents of heavy metals and metalloids by 33-99%; the portion of elements fixed on the geochemical barriers increased by 26-50%.

Geochemical signature of columbite-tantalite and environmental impact of radioactive pegmatite mining in the Parelhas region, Rio Grande do Norte, Northeast Brazil

International Nuclear Information System (INIS)

Moura, Jorge Costa de; Cruz, Paulo R.; Pereira, Valmir; Ludka, Isabel P.; Mendes, Julio C.

2013-01-01

This article comprises geochemical, structural and radiometric investigations on radioactive pegmatites of the Borborema Pegmatitic Province in Northeast Brazil. The studied area is located in the surroundings of the city of Parelhas, in the geotectonic Province of Borborema. It is well known for its thousands of pegmatitic bodies exploited in primitive mines called garimpos. The main goal was to find an efficient, cheap and routine inspection procedure to identify the origin of commercialized radioactive columbite-tantalite (coltan) ore. The Brazilian Nuclear Energy Agency (CNEN) controls uranium commerce and nuclear activity in Brazil. Without an effective method to characterize coltan ores from different localities it is impossible to control the trade. The here presented new method was developed by correlating structural features of these pegmatites with the geochemical behavior of their coltan samples. It was found that the variation of U/Th vs. Nb 2 O 5 /Ta 2 O 5 provides geochemical signatures (analytical fingerprints) for the source location of such ore. The new method was tested with coltan samples of commercial batches from the Brazilian states of Amapa and Rondonia and also generated distinct geochemical signatures. A radiometric survey (CPS) to study the environmental impact of gamma radiation was also carried out in several mines and pegmatites. It included in situ measurements of pegmatite walls, enclosing rocks, soil, and accumulated water and revealed that gamma emitters are hardly solubilized and therefore environmental gamma radiation generally is not enhanced to a dangerous level. (author)

Geotechnical and geochemical assessments of shales in Anambra basin, SE-Nigeria as compacted clay liner in landfill system

International Nuclear Information System (INIS)

Tijani, Moshood N.; Adesina, Rasheed B.; Wagner, Jean-Frank

2012-01-01

Document available in extended abstract form only. A major constraint to the development of properly engineered landfills is the high cost of synthetic liners and its scarcity in the local markets in developing country like Nigeria, which calls for alternative local materials for landfill liner. Consequently, crushed shale / clay shale deposits appear inexpensive and can be utilized to effectively retard the spread of leachate from landfills. Hence, this study focus on the assessment of geotechnical, geochemical and sorption characteristics of shale units from Anambra Basin, SE-Nigeria for suitability or otherwise as compacted clay liner (CCL) in landfills. Twelve samples consisting of three each from four different formations namely: Enugu, Nkporo, Imo and Ameki formations were collected and subjected to basic geotechnical tests such as grain size analysis, Atterberg's limits, compaction and coefficient of permeability following standard testing methods (BS 1377). In addition, mineralogical X-ray Diffraction (XRD) and geochemical ICP-MS / ICP-ES analyses were employed for geochemical characterization. CEC and batch sorption tests with respect to Pb, Ni, Cd, Cu and Zn as contaminant in leachates were also employed for sorption characterization. The results of the geotechnical tests conducted on the shale samples revealed that the crushed shale samples have liquid limit range of 55-79%, percentage fines of 80-93%, percentage clay of 23- 36% and activity of 0.8-2.1, all of which satisfy the basic requirements of clay liners according to the specifications of Daniel, 1993. Samples from Enugu, Nkporo and Imo shale have plasticity index range of 40- 54% which is above the recommended limit of 35% and thus likely to exhibit excessive shrinkage and settlement. However, the laboratory compaction shows maximum dry density of 16.8-18.4 kN/m 3 and 17.3- 19.1 kN/m 3 respectively for Standard Proctor and Modified AASHTO energy levels which suggests no significant change the

Geochemical prospecting for copper and nickel in the Wulgai and Tor Tangi areas southeast of Hindubagh, Quetta Division, Pakistan

Science.gov (United States)

Stanin, S. Anthony; Wahid, M.A.; Khan, Shamsher

1975-01-01

Showings of magnetite, copper, and possible nickel mineralization in the Hindubagh chromite mining district are near Wulgai and Tor Tangi. Several hundred samples of clastic material from dry streambeds in these areas were sieved for the minus-80-mesh fraction and analyzed for copper using 2, 2'-biquinoline and for nickel using alpha-furildioxime. The copper threshold is 75 ppm, and the nickel threshold is 400 ppm. A geochemical map has been prepared that shows nine areas of anomalously high copper and six areas of high nickel. The nickel anomalies may represent secondary dispersion patterns derived from the erosion of nickeliferous ultramafic rocks of the Hindubagh intrusive complex. Copper showings in and near four of the anomalous copper areas indicate that detailed geological investigation and detailed geochemical sampling of rocks, soil, and unconsolidated clastic material are required to determine the source of the anomalies.

Geochemical modelling. Pt.1, Pt.2

International Nuclear Information System (INIS)

Skytte Jensen, B.; Jensen, H.; Pearson, F.J.

1992-01-01

This work is carried out under cost-sharing contract with the European Atomic Energy Community in the framework of its fourth research programme on radioactive waste management and radioactive waste storage. This final report is subdivided into two parts. In the first part, JENSEN, a computer code for the computation of chemical equilibria in aqueous systems, describes the structure, function and use of a new geochemical computer program intended for PC's. The program, which is written in Turbo Pascal, version 4, is fundamentally similar to most other geochemical programs, but combines in one program several of the merits these programs have. The intention has been to make an advanced program, which also should be user friendly and fast, and to attain this several new algorithms have been developed and implemented. The program has a built-in database mainly based on the CHEMVAL compilation containing data for 395 soluble species and 149 minerals. The program can find equilibria in the presence of all or some of these soluble species, under conditions or fixed or floating pH and / or Redox potential. The program by itself eliminates a bad guess of a candidate for precipitation. In the present version, the program can identify which minerals and how much of them there will be formed when equilibrium is established. In the second part, LITTLE JOE, an expert system to support geochemical modelling, describes the construction of a minor expert system for use in the evaluation of analytical data for the composition of ground waters from limestone formation. Although the example given is rather limited in scope, the application of the expert system for the evaluation of the analytical data clearly demonstrates the mature expert knowledge imbedded in the system which is contrasted with the uncritical acceptance of analytical or theoretical data. With the overall neglect of ion-exchange and the formation of solid solutions in geochemical calculations, geochemistry is

Geochemical evaluation of marginal basins in the south of Bahia state, Brazil

International Nuclear Information System (INIS)

Gaglianone, P.C.; Trindade, L.A.F.; Nascimento, M.M. do

1987-01-01

Geochemical analyses were performed on more than 700 rock samples and 4 oil samples, from Mucuri, Cumuruxatiba and Jequitinhonha basins, offshore Bahia state, Brazil. The methods employed in this study includes the evaluation of organic carbon contents, Rock-Eval pyrolysis, vitrinite reflectance, carbon isotopes, assessment of oils and extrats by liquid and gas chromatography and gas chromatography - spectrometry. Three main source rock systems have been identified in offshore Bahia: the Mucuri shales from Rio da Serra and Aratu Stages lower Neocomian related to a lacustrine fresh water environment; the Jiquia shales (Upper Neocomian) deposited in a lacustrine saline water environment, and the Alagoas Shales related to an evaporitic environment of Aptian age. (author) [pt

Geochemical modelling of groundwater evolution using chemical equilibrium codes

International Nuclear Information System (INIS)

Pitkaenen, P.; Pirhonen, V.

1991-01-01

Geochemical equilibrium codes are a modern tool in studying interaction between groundwater and solid phases. The most common used programs and application subjects are shortly presented in this article. The main emphasis is laid on the approach method of using calculated results in evaluating groundwater evolution in hydrogeological system. At present in geochemical equilibrium modelling also kinetic as well as hydrologic constrains along a flow path are taken into consideration

Determination of geochemical characters of insterstitial waters of pleistocene Italian clay formations

International Nuclear Information System (INIS)

Fontanive, A.; Gragnani, R.; Mignuzzi, C.; Spat, G.

1985-01-01

The geochemical characters of clay formations and of their pore water are fundamental with regards to the mobility of the radionuclides as well as to the corrosion processes on enginered barriers. Experimental researches have been carried out in different types of clay, which represent Italian formations, for the characterization of pore water. A squeezer system, which reaches 1500 Kg/cm 2 in pressure, and an analytical micro-scale methodology, for the determination of dissolved constituents in pore water, were set up. The extracted pore water ranges from 60% to 85% in relation to consolidation state of clay. The chemical composition of the extracted fluid has been checked during the squeezing. During this step the observed variations were smaller than those between the different specimens of the same sample. The comparison between the results obtained by squeezing and by a multiple washing technique, using increasing water/sediment ratios, shows that the last one does not give reliable results on the chemical composition of pore water. This is due to the presence of easily weatherable minerals and to the exchange processes between the clayey minerals and the solution. Nevertheless both these techniques have supplied complementary information about geochemical processes in water-rock interaction. The salinity of pore water ranges from 0.45 g/l to 24.5 g/l and the chemism always shows a high content of calcium-magnesium sulfate, or sodium chloride or calcium-magnesium-sulfate with sodium chloride. The correlation between geochemical composition of pore water and mineralogical composition of clay is not significant

Behaviour of nature and technogenic radioisotopes in buried geochemical barriers

International Nuclear Information System (INIS)

Kuznetsov, V.A.; Onoshko, M.P.; Generalova, V.A.

1998-01-01

Behaviour of potassium 40, radium 226, thorium 232, strontium 90 and cesium 137 on geochemical barriers connected with buried soils and cut-off meander sediments of the Holocene age of the Sozh river valley are examined. Some sides of the barrier geochemical structure caused by syngeneic and epigenetic processes have been taken into consideration

Research on the hydrogeological and geochemical conditions at the coastal area and submarine formations

International Nuclear Information System (INIS)

Tokunaga, Tomochika; Taniguchi, Makoto; Goto, Junji

2003-05-01

One of the major concerns for the high-level radioactive waste disposal is the possibility of the radionuclides to reach biosphere by groundwater flow. Recent research results have shown that the fresh groundwater discharge from subsea formations are widespread phenomena, thus, it is necessary to evaluate the submarine groundwater discharge as possible pathways of contaminant discharge towards the biosphere. It is also important to unravel the groundwater flow and associated material transport at the coastal area and subsea formations. To better understand the groundwater flow processes and the submarine groundwater discharge, we have conducted the hydrological, hydrogeological, geochemical, and numerical modeling studies at the Kurobe alluvial fan and its offshore, Toyama Prefecture, Japan. In this report, the results of the following research activities are presented: 1) Development and application of a method to detect the locations of the submarine groundwater discharge. 2) Development and application of a method to collect uncontaminated groundwater samples from subsea formations. 3) Measurements of submarine groundwater discharge fluxes by automated seepage meter. 4) Hydrological and geochemical studies for groundwater flow at the coastal area. 5) Geochemical studies to understand sources of fresh submarine groundwater discharge. 6) Examination of groundwater flow and submarine groundwater discharge using methane concentration and carbon isotope ratio. 7) Numerical modeling studies for coastal groundwater flow system. (author)

An organic geochemical correlation study of some Drmno depresssion crude oils (southern part of the Pannonian Basin, Yugoslavia

Directory of Open Access Journals (Sweden)

D. VITOROVIC

2001-05-01

Full Text Available The results of an investigation of crude oils originating from the Sirakovo and Bradarac-Maljurevac localities (southern part of the Pannonian Basin are reported in this paper. The aim was to estimate the organic geochemical similarity of the crude oils from the Drmno (Kostolac depression oil fields. The nine selected samples originated from reservoir rocks of various depths. Reliable source and organic geochemical maturation parameters served as the basis for the correlation studies. The similar origin of the investigated Drmno depression crude oils was corroborated, characterized by a significant participation of terrestrial precursor biomass. They were shown to be of relatively low maturity and to have been formed during the earlier stages of the diagenet- ic-catagenetic sequence of processes leading to the formation of crude oils, most probably in source rocks ofTertiary age, corresponding to vitrinite reflectances between Ro = 0.70 % and Ro = 0.80 %. The crude oils from Bradarac-Maljurevac seemed to be somewhat less homogeneous with respect to organic geochemical parameters compared to Sirakovo crude oils.

Data precision of X-ray fluorescence (XRF) scanning of discrete samples with the ITRAX XRF core-scanner exemplified on loess-paleosol samples

Science.gov (United States)

Profe, Jörn; Ohlendorf, Christian

2017-04-01

XRF-scanning is the state-of-the-art technique for geochemical analyses in marine and lacustrine sedimentology for more than a decade. However, little attention has been paid to data precision and technical limitations so far. Using homogenized, dried and powdered samples (certified geochemical reference standards and samples from a lithologically-contrasting loess-paleosol sequence) minimizes many adverse effects that influence the XRF-signal when analyzing wet sediment cores. This allows the investigation of data precision under ideal conditions and documents a new application of the XRF core-scanner technology at the same time. Reliable interpretations of XRF results require data precision evaluation of single elements as a function of X-ray tube, measurement time, sample compaction and quality of peak fitting. Ten-fold measurement of each sample constitutes data precision. Data precision of XRF measurements theoretically obeys Poisson statistics. Fe and Ca exhibit largest deviations from Poisson statistics. The same elements show the least mean relative standard deviations in the range from 0.5% to 1%. This represents the technical limit of data precision achievable by the installed detector. Measurement times ≥ 30 s reveal mean relative standard deviations below 4% for most elements. The quality of peak fitting is only relevant for elements with overlapping fluorescence lines such as Ba, Ti and Mn or for elements with low concentrations such as Y, for example. Differences in sample compaction are marginal and do not change mean relative standard deviation considerably. Data precision is in the range reported for geochemical reference standards measured by conventional techniques. Therefore, XRF scanning of discrete samples provide a cost- and time-efficient alternative to conventional multi-element analyses. As best trade-off between economical operation and data quality, we recommend a measurement time of 30 s resulting in a total scan time of 30 minutes

Geochemical reversals within the lower 100 m of the Palisades sill, New Jersey

Science.gov (United States)

Gorring, Matthew L.; Naslund, H. R.

1995-03-01

Transects through the lower part of the Palisades sill were made at Fort Lee and Alpine, New Jersey in order to characterize the petrologic signature of previously proposed “reversals” in the normal, tholeiitic differentiation trend. Petrographic and geochemical data include: (1) modal and grain size analyses, (2) bulk rock major and trace element concentrations by DCP-AES, and (3) augite, orthopyroxene, magnetite, and olivine compositions by electron microprobe analysis. Anomalous horizons, defined by increased bulk rock Mg?, Cr, Ni, and Co concentrations and abrupt modal and grain-size changes, occur at 10 m (the well known olivine zone), 27 m, 45 m, and 95 m above the basal contact. Thermal models coupled with estimates of the emplacement rate and total magma volume indicate that the olivine zone (OZ) is an early-stage feature, related to the emplacement of initial magma into the Palisades chamber. Stoke’s Law calculations indicate that the settling velocity of average-sized olivine crystals in a high-titanium, quartz-normative (HTQ) magma is too slow for significant gravity settling to have occurred prior to the solidification of the basal 20 m of the sill. It is suggested that the OZ resulted from the emplacement of a heterogeneous initial magma from a compositionally stratified, sub-Palisades storage chamber located within the upper crust; however, heterogeneity may have been derived directly from the mantle or during rapid ascent. Geochemical models indicate that the OZ contains accumulated olivine that is not in cotectic (or constant) proportions with the other cumulus phases, suggesting a mechanical sorting process. Magma chamber recharge is proposed to have occurred at the 27 m and 45 m levels, when a slightly more-primitive HTQ magma was injected into the Palisades sill cha- mber. Zones of elevated Mg? and Cr, 6 to 10 m thick, at these two horizons may indicate the thickness of the hybrid magma formed by the mixing of these two compositions

Historical reconstruction of oil and gas spills during moderate and strong earthquakes and related geochemical surveys in Southern Apennines

Science.gov (United States)

Sciarra, Alessandra; Cantucci, Barbara; Ferrari, Graziano; Pizzino, Luca; Quattrocchi, Fedora

2016-04-01

The aim of this study is to contribute to the assessment of natural hazards in a seismically active area of southern Italy through the joint analysis of historical sources and fluid geochemistry. In particular, our studies have been focalized in the Val d'Agri basin, in the Apennines extensional belt, since it hosts the largest oilfield in onshore Europe and normal-fault systems with high seismogenic potential (up to M7). The work was organized into three main themes: 1) literature search aimed at identifying fluid emissions during previous moderate-strong earthquakes; 2) consultation of local and national archives to identify historic local place names correlated to natural fluids emissions; 3) geochemical sampling of groundwater and gas issuing at surface, identified on the basis of the bibliographic sources. A reasoned reading of written documents and available historical data was performed. Moreover, we reworked information reported in historical catalogues, referred to liquid and gas hydrocarbon leakages occurred during seismic events of the past (in a range of magnitude from 5 to 7) in the Southern Apennines (with a particular focus on the Val d'Agri). Special attention was given to the phenomena of geochemical emissions related to major historical earthquakes that took place in the area, most notably that of 16 December 1857 (M = 7). A careful analysis of the Robert Mallet's report, a complete work aimed at describing the social impact and the effects on the environment produced by this earthquake through illustrated maps and diagrams, included several hundred monoscopic and stereoscopic photographs, was done. From archival sources (at national and/or local administrations), "sensitive" sites to the onset of leakage of liquid and gaseous hydrocarbons in the past were identified. A soil-gas survey (22 gas concentrations and flux measurements) and 35 groundwater samplings were carried out in specific sites recognized through the above studies. From a

Signatures of geochemical changes at methane-seeps as recorded by seep carbonates

OpenAIRE

Himmler, Tobias

2011-01-01

This thesis compiles three manuscripts: (1) The first manuscript (chapter 2.1) contains petrographic and geochemical data of aragonitic seep carbonates from the Makran accretionary prism. High-resolution rare earth element (REE) analysis yield distinct total REE[aragonite] concentrations and shale-normalised REE[aragonite] patterns. The REE variations are ascribed to different pore fluid compositions and accompanied redox changes during aragonite precipitation. (2) The second manuscript (chap...

The identification of provenance-controlled facies by geochemical methods on a portion of the Vaal Reef, Klerksdorp Goldfield

International Nuclear Information System (INIS)

Henckel, J.; Schweitzer, J.K.; Horsch, H.

1990-01-01

The use of geochemical methods for identifying provenance controlled facies in Witwatersrand reefs is considered. Three methods - whole rock geochemistry, zircon analysis, and chromite analysis - have been evaluated in order to establish the feasibility of using these geochemical techniques. An area of Vaal Reef where two sedimentological facies with distinct gold distributions had previously been identified was investigated. The studies reported here gave evidence of differences in the source areas for these two facies. Accordingly, it is concluded that the application of geochemistry to identify provenance-controlled facies is a useful technique which can help geologists arrive at a better interpretation of depositional systems within Witwatersrand reefs and thereby assist in the understanding of gold distribution patterns. 26 refs., 11 figs., 4 tabs

GEOBASI: The geochemical Database of Tuscany Region (Italy

Directory of Open Access Journals (Sweden)

Brunella Raco

2015-03-01

Full Text Available In this study the new Regional Geochemical Database (RGDB, called GEOBASI, is presented and illustrated in the framework of a joint collaboration among the three Tuscan universities (Florence, Pisa and Siena, CNR-IGG (Institute of Geosciences and Earth Resources of Pisa, ARPAT (Regional Agency for the Environmental Protection, LAMMA (Environmental Modelling and Monitoring Laboratory for Sustainable Development Consortium and S.I.R.A. (Territorial and Environmental Informative System of Tuscany. The database has permitted the construction of a repository where the geochemical information (compositional and isotopic has been stored in a structured way so that it can be available for different groups of users (e.g. institutional, public and private companies. The information contained in the database can in fact be downloaded freely and queried to correlate geochemistry to other non compositional variables. The first phase of the project was aimed at promoting the use of the geochemical data already available from previous investigations through a powerful Web-GIS interface to implement the exploratory statistics graphical-numerical tools used to: 1 analyse the spatial variability of the investigated context, 2 highlight the geographic location of data pertaining to classes of values or single cases, 3 compare the results of different analytical methodologies applied to the determination of the same element and/or chemical species, 4 extract the geochemical data related to specific monitoring plans and/or geographical areas, and finally 5 recover information about data below the detection limit to understand their impact on the behaviour of the investigated variable. Developments of this project will be focused on the definition of rules and standardized methods in a way that external users could also interactively pursue the RGDB. Furthermore, a detailed investigation of the Scarlino-Follonica plain will permit the improvement and test of

Geochemical Anomalies in the Sediments of Lake Druksiai

International Nuclear Information System (INIS)

Kleinas, A.

1999-01-01

In order to evaluate the impact of Ignalina Nuclear Power Plant (NPP) on natural processes in Lake Druksiai and accumulation of pollutants, in 19931997, carrying on the state scientific program, the Marine Geochemistry Division of the Institute of Geography performed lithological geochemical mapping of lake bottom sediments on a scale of 1 .50 000. The results obtained enabled to distinguish zones of higher anthropogenous geochemical load, where geochemical anomalies of pollutants, including oil hydrocarbons and heavy metals, had been taken into account. Applying concentration coefficients for oil hydrocarbons and heavy metals (Cr, Cu, Ni, Pb, and Zn) and their natural background, the attempt was made to differentiate natural and technogenous components in the geochemical anomalies As expected, the finer sediments -aleurite-pelite mud - showed amounts of oil hydrocarbons and heavy metals being 12.1 times higher than in fine sand - the most coarse of the sediments studied Sediments with organic mater exceeding 20% contained 11.7 times more pollutants than those with organic matter below 1 .5%. Calculations of concentration coefficients (CC) showed no elements in no stations exceeded 10 - the sediments did not reach the category of high pollution However, in many sites, the coefficients exceeded values of 1-2, thus, showing sediments attributable to the categories of weakly polluted or just polluted. Mapping model done by GIS methods (by superimposing schemes of pollutant CCs distribution in the lake and summing them) for geochemical anomalies two derivative map-schemes were obtained for oil hydrocarbons and heavy metals. They showed that clean sediments cover just 24.75% (according to the pollutant background for soil types) and 12.35% (according to the organic matter background for its amount intervals) lake bottom area. Zones slightly polluted by an element at least cover 69.7 and 80.29% of lake area, correspondingly; whereas zones slightly polluted by all

Reconnaisance geochemical survey of heavy minerals in Northern Luzon, Philippines

International Nuclear Information System (INIS)

Santos, G. Jr.; Seguis, J.E.; Fernandez, L.G.

1983-07-01

A reconnaissance sampling was undertaken in northern Luzon to study the distribution of uranium as well as copper, lead, zinc, manganese, silver, cobalt and nickel in heavy minerals. The average background and threshold values of the elements were determined. Uranium content in the heavy mineral was low, in the order of 0.5-0.6 ppm U. Three uranium anomaly zones were delineated in Malanas Rever-Licuan area, Abra, Itogon, Benguet and Bambang, Nueva Viscaya, all within the Central Cordillera. The anomalous zones appeared to be related to copper-gold mineral areas. Geochemical correlations between uranium and the other elements were generally poor. (author)

Stream sediment detailed geochemical survey for Marysvale, Utah

International Nuclear Information System (INIS)

Butz, T.R.; Vreeland, J.L.; Bard, C.S.; Helgerson, R.N.; Grimes, J.G.; Pritz, P.M.

1980-01-01

Results of the Marysvale detailed geochemical survey are reported. Field and laboratory data are presented for 397 stream sediment samples and 160 radiometric readings. Statistical and areal distributions of uranium and possible uranium-related variables are displayed. A generalized geologic map of the area is provided, and pertinent geologic factors which may be of significance in evaluating the potential for uranium mineralization are briefly discussed. Stream sediments containing significant amounts of soluble uranium (greater than or equal to 16.93 ppM) occur in numerous areas, the most prevalent being in the western portion of the survey area, within and surrounding the Mount Belknap Caldera. Thorium, beryllium, cerium, manganese, molybdenum, niobium, potassium, yttrium, zinc, and zirconium occur in concentrations greater than or equal to 84th percentile in many sediment samples taken from within and surrounding the Mount Belknap Caldera. The uranium and related variables are associated with highly silicic intrusions and extrusions of the Mount Belknap Volcanics, as well as hydrothermal activity which has occurred in the Marysvale volcanic field

The geochemical environment of nuclear fuel waste disposal

International Nuclear Information System (INIS)

Gascoyne, M.

1995-01-01

The concept for disposal of Canada's nuclear fuel waste in a geologic environment on the Canadian Shield has recently been presented by Atomic Energy of Canada Limited (AECL) to governments, scientists, and the public, for review. An important part of this concept concerns the geochemical environment of a disposal vault and includes consideration of rock and groundwater compositions, geochemical interactions between rocks, groundwaters, and emplaced vault materials, and the influences and significance of anthropogenic and microbiological effects following closure of the vault. This paper summarizes the disposal concept and examines aspects of the geochemical environment. The presence of saline groundwaters and reducing conditions at proposed vault depths (500-1000 m) in the Canadian Shield has an important bearing on the stability of the used nuclear fuel, its container, and buffer and backfill materials. The potential for introduction of anthropogenic contaminants and microbes during site investigations and vault excavation, operation, and sealing is described with examples from AECL's research areas on the Shield and in their underground research laboratory in southeastern Manitoba. (author)

Well sediments: a medium for geochemical prospecting, an example from the Nisa region, Portugal

NARCIS (Netherlands)

Vriend, S.P.; Dekkers, M.J.; Janssen, M.A.; Commandeur, J.

1991-01-01

Vriend, S.P., Dekkers, M.J.. Janssen, M.A. and Commandeur, J., 1991. Well sediments: a medium for geochemical prospecting, an example from the Nisa region. Portugal. In: A.W. Rose and P.M. Taufen I Editors). Geochemical Exploration ! 989. J. Geochem. Expior., 4 ! : ! 5 I- 167. Tile potential of

Hydro-geochemical modeling of subalpine urbanized area: geochemical characterization of the shallow and deep aquifers of the urban district of Como (first results).

Science.gov (United States)

Terrana, Silvia; Brunamonte, Fabio; Frascoli, Francesca; Ferrario, Maria Francesca; Michetti, Alessandro Maria; Pozzi, Andrea; Gambillara, Roberto; Binda, Gilberto

2016-04-01

One of the greatest environmental and social-economics threats is climate change. This topic, in the next few years, will have a significant impact on the availability of water resources of many regions. This is compounded by the strong anthropization of water systems that shows an intensification of conflicts for water resource exploitation. Therefore, it is necessary a sustainable manage of natural resources thorough knowledge of the hosting territories. The development of investigation and data processing methods are essential to reduce costs for the suitable use and protection of resources. Identify a sample area for testing the best approach is crucial. This research aims to find a valid methodology for the characterization, modeling and management of subalpine urban aquifers, and the urban district of Como appears perfect. The city of Como is located at the southern end of the western sector of Lake Como (N Italy). It is a coastal town, placed on a small alluvial plain, therefore in close communication with the lake. The plain is drained by two streams, which are presently artificially buried, and have an underground flow path in the urban section till the mouth. This city area, so, is suitable for this project as it is intensely urbanized, its dimensions is not too extensive and it is characterized by two aquifers very important and little known. These are a shallow aquifer and a deep aquifer, which are important not only for any water supply, but also for the stability of the ground subsidence in the city. This research is also the opportunity to work in a particular well-known area with high scientific significance; however, there is complete absence of information regarding the deep aquifer. Great importance has also the chosen and used of the more powerful open source software for this type of area, such as PHREEQC, EnvironInsite, PHREEQE etc., used for geological and geochemical data processing. The main goal of this preliminary work is the

Current approaches to geochemical reconnaissance for uranium in the Canadian Shield

International Nuclear Information System (INIS)

Cameron, E.M.; Hornbrook, E.H.W.

1976-01-01

Wide-interval geochemical reconnaissance is currently being carried out over large areas of the Canadian Shield by the Geological Survey of Canada. This work is in support of the federal-provincial Uranium Reconnaissance Program. The paper reviews the methodology employed for this reconnaissance to outline areas of enhanced potential for uranium and other mineral commodities. The generally low relief of the Shield virtually restricts wide-interval reconnaissance to the mobile elements that can travel some distance in solution. The high mobility of uranium, particularly in waters of neutral pH, makes it one of the most suitable types of mineralization for detection. For much of the Shield the most appropriate sampling media are lake sediments and lake waters. Centre-lake sediments are homogeneous, and are readily and economically collected utilizing helicopter support. They provide a good response for uranium and a variety of other indicator elements. Waters collected at the same sample sites are a useful supplement in the search for uranium mineralization, particularly in carbonate terrain. However, because of the very low content of uranium in many Shield waters, they present as yet unresolved problems of analysis and storage. The influence of organic material, iron and manganese on the uranium content of lake sediments are examined. Their scavenging influence has been found to be significant only at their lower concentration levels, particularly for organic matter and iron. For the majority of centre-lake samples the effect is negligible. The choice of sample interval is related to total survey costs, to speed of coverage, and to ability to detect uranium and other types of mineralization. For current G.S.C. programs a sample density of one per five square mile appears optimal. The results are presented as l:250,000 symbol maps that are prepared largely by computer, and as 1:1,000,000 contoured compilation maps. (author)

Baseline and premining geochemical characterization of mined sites

Science.gov (United States)

Nordstrom, D. Kirk

2015-01-01

A rational goal for environmental restoration of new, active, or inactive mine sites would be ‘natural background’ or the environmental conditions that existed before any mining activities or other related anthropogenic activities. In a strictly technical sense, there is no such thing as natural background (or entirely non-anthropogenic) existing today because there is no part of the planet earth that has not had at least some chemical disturbance from anthropogenic activities. Hence, the terms ‘baseline’ and ‘pre-mining’ are preferred to describe these conditions. Baseline conditions are those that existed at the time of the characterization which could be pre-mining, during mining, or post-mining. Protocols for geochemically characterizing pre-mining conditions are not well-documented for sites already mined but there are two approaches that seem most direct and least ambiguous. One is characterization of analog sites along with judicious application of geochemical modeling. The other is reactive-transport modeling (based on careful synoptic sampling with tracer-injection) and subtracting inputs from known mining and mineral processing. Several examples of acidic drainage are described from around the world documenting the range of water compositions produced from pyrite oxidation in the absence of mining. These analog sites provide insight to the processes forming mineralized waters in areas untouched by mining. Natural analog water-chemistry data is compared with the higher metal concentrations, metal fluxes, and weathering rates found in mined areas in the few places where comparisons are possible. The differences are generally 1–3 orders of magnitude higher for acid mine drainage.

Vertical evolution of petrographic and organic geochemical parameters in Las Duenas mire (Cantabrian Coast, North Spain)

Energy Technology Data Exchange (ETDEWEB)

Lopez-Dias, V.; Borrego, A.G.; Blanco, C.G. [Instituto Nacional del Carbon (CSIC), Oviedo (Spain)

2010-12-01

Las Duenas mire has developed on a flat siliceous substrate over the Holocene. The sedimentary cover has a thickness of around 50 cm and the mire comprises a surface area of 27 ha. A core sample obtained using a manual probe was split into sub-samples of around 3-4 cm thickness for petrographic and organic geochemical analysis. The fen originated by minerogenesis and contains a high concentration of mineral matter throughout its profile which decreases towards the top. The present day vegetation is dominated by Sphagnum. A variety of transparent textinite with intense fluorescence is evidence of the low maturity of the profile, which is also confirmed by the presence of low reflecting huminite of the A variety (Hr {proportional_to} 0.15%). The fluorescence spectra of sporinite and cutinite are similar and, compared with those of transparent textinite, they have a lower intensity and are shifted to higher wavelengths. The low maturity of the organic matter is also confirmed by the presence of unstable {beta}{beta} hopane configurations, the abundance of hopene, and the presence of functionalized hopanoids, steroids and other triterpenoids. The evolution of the geochemical parameters in the peat profile indicates the presence of more humid conditions in the top 4 cm and at a depth of 11-15 cm. These periods are characterized by a high Sphagnum/higher plant contribution as deduced from the n-alkane ratios. The low reflectance of huminite at the depth of 11-15 cm could also support less oxidizing condition. The sediment at a depth of 22 cm where peaty matter starts to accumulate has been dated as 9603 cal BC, whereas the plant fraction at the same depth dates back to a maximum of 200 years. Sediment reworking derived from radiocarbon dates indicates that this fen is not suitable for palaeoenvironmental studies. (author)

Geochemical and Pb, Sr, and O isotopic study of the Tiva Canyon Tuff and Topopah Spring Tuff, Yucca Mountain, Nye County, Nevada

International Nuclear Information System (INIS)

Neymark, L.A.; Marshall, B.D.; Kwak, L.M.; Futa, Kiyoto; Mahan, S.A.

1995-01-01

Yucca Mountain is currently being studied as a potential site for an underground repository for high-level radioactive waste. One aspect of the site characterization studies is an evaluation o the resource potential at Yucca Mountain. Geochemical and isotopic signatures of past alteration of the welded tuffs that underlie Yucca Mountain provide a means of assessing the probability of hydrothermal ore deposits being present within Yucca Mountain. In this preliminary report, geochemical and isotopic measurements of altered Tiva Canyon Tuff and Topopah Spring Tuff collected from fault zones exposed on the east flank of Yucca Mountain and from one drill core are compared to their unaltered equivalents sampled both in outcrop and drill core. The geochemistry and isotopic compositions of unaltered Tiva Canyon Tuff and Topopah Spring Tuff (high-silica rhyolite portions) are fairly uniform; these data provide a good baseline for comparisons with the altered samples. Geochemical analyses indicate that the brecciated tuffs are characterized by addition of calcium carbonate and opaline silica; this resulted in additions of calcium and strontium,increases in oxygen-18 content, and some redistribution of trace elements. After leaching the samples to remove authigenic carbonate, no differences in strontium or lead isotope compositions between altered and unaltered sections were observed. These data show that although localized alteration of the tuffs has occurred and affected their geochemistry, there is no indication of additions of exotic components. The lack of evidence for exotic strontium and lead in the most severely altered tuff samples at Yucca Mountain strongly implies a similar lack of exotic base or precious metals

Validation of the WATEQ4 geochemical model for uranium

International Nuclear Information System (INIS)

Krupka, K.M.; Jenne, E.A.; Deutsch, W.J.

1983-09-01

As part of the Geochemical Modeling and Nuclide/Rock/Groundwater Interactions Studies Program, a study was conducted to partially validate the WATEQ4 aqueous speciation-solubility geochemical model for uranium. The solubility controls determined with the WATEQ4 geochemical model were in excellent agreement with those laboratory studies in which the solids schoepite [UO 2 (OH) 2 . H 2 O], UO 2 (OH) 2 , and rutherfordine ((UO 2 CO 3 ) were identified as actual solubility controls for uranium. The results of modeling solution analyses from laboratory studies of uranyl phosphate solids, however, identified possible errors in the characterization of solids in the original solubility experiments. As part of this study, significant deficiencies in the WATEQ4 thermodynamic data base for uranium solutes and solids were corrected. Revisions included recalculation of selected uranium reactions. Additionally, thermodynamic data for the hydroxyl complexes of U(VI), including anionic (VI) species, were evaluated (to the extent permitted by the available data). Vanadium reactions were also added to the thermodynamic data base because uranium-vanadium solids can exist in natural ground-water systems. This study is only a partial validation of the WATEQ4 geochemical model because the available laboratory solubility studies do not cover the range of solid phases, alkaline pH values, and concentrations of inorganic complexing ligands needed to evaluate the potential solubility of uranium in ground waters associated with various proposed nuclear waste repositories. Further validation of this or other geochemical models for uranium will require careful determinations of uraninite solubility over the pH range of 7 to 10 under highly reducing conditions and of uranyl hydroxide and phosphate solubilities over the pH range of 7 to 10 under oxygenated conditions

Variation of Geochemical Signatures and Correlation of Biomarkers in Icelandic Mars Analogue Environments

Science.gov (United States)

Gentry, D.; Amador, E. S.; Cable, M. L.; Cantrell, T.; Chaudry, N.; Cullen, T.; Duca, Z. A.; Jacobsen, M. B.; McCaig, H. C.; Murukesan, G.; Rennie, V.; Schwieterman, E. W.; Stevens, A. H.; Tan, G.; Yin, C.; Stockton, A.; Cullen, D.; Geppert, W.

2015-12-01

Exploration missions to Mars rely on rovers to perform deep analyses over small sampling areas; however, landing site selection is done using large-scale but low-resolution remote sensing data. Using Earth analogue environments to estimate the small-scale spatial and temporal distributions of key geochemical signatures and (for habitability studies) biomarkers helps ensure that the chosen sampling strategies meet mission science goals. We conducted two rounds of analogue expeditions to recent Icelandic lava fields. In July 2013, we tested correlation between three common biomarker assays: cell quantification via fluorescence microscopy, ATP quantification via bioluminescence, and quantitative PCR with universal primer sets. Sample sites were nested at four spatial scales (1 m, 10 m, 100 m, and > 1 km) and homogeneous at 'remote imaging' resolution (overall temperature, apparent moisture content, and regolith grain size). All spatial scales were highly diverse in ATP, bacterial 16S, and archaeal 16S DNA content; nearly half of sites were statistically different in ATP content at α = 0.05. Cell counts showed significant variation at the 10 m and 100 m scale; at the > 1 km scale, the mean counts were not distinguishable, but the median counts were, indicating differences in underlying distribution. Fungal 18S DNA content similarly varied at 1 m, 10 m, and 100 m scales only. Cell counts were not correlated with ATP or DNA content at any scale. ATP concentration and DNA content for all three primer sets were positively correlated. Bacterial DNA content was positively correlated with archaeal and fungal DNA content, though archaeal correlation was weak. Fungal and archaeal correlation was borderline. In July 2015, we repeated the sampling strategy, with the addition of a smaller-scale sampling grid of 10 cm and a third > 1 km location. This expedition also measured reflectance of the tephra cover and preserved mineral samples for future Raman spectroscopy in order to

Optimum sampling scheme for characterization of mine tailings

CSIR Research Space (South Africa)

Debba, Pravesh

2009-07-01

Full Text Available The paper describes a novice method for sampling geochemicals to characterize mine tailings. The author’s model the spatial relationships between a multi-element signature and, as covariates, abundance estimates of secondary iron-bearing minerals...

Testing and sampling of deep brine aquifers in the Palo Duro Basin, West Texas

International Nuclear Information System (INIS)

Deyling, M.A.

1984-01-01

The US Department of Energy is investigating the Palo Duro Basin of West Texas along with locations in Nevada, Washington, Utah, Mississippi and Louisiana as potential sites for storage of high-level nuclear waste. Ten wells have been drilled to depths between 3000 and 8300 feet. Testing and sampling of deep test zones requires advance planning and analysis of what must be obtained from the well. Various alternatives are available depending on data needs. In this particular instance, both hydrologic and geochemical data were required. The methods chosen were field proven methods used in the oil field industry for many years. Short term testing has included conventional oil-field-type drill stem tests and drill stem equipment with surface pressure readout. Long term testing has consisted of a series of production and recovery tests. Fluid sampling was performed in two stages. The first was at the well head under an imposed pressure of several hundred psi. The second fluid samples were collected downhole at the production zone under pressures close to ambient pressure. The geochemical data and hydrologic data can be used as independent checks on each other in many cases. Test results from the well along with examination of recovered core provided maximum data for each well. 5 references, 8 figures

Geochemical and isotopic evidences for a severe anthropogenic boron contamination: A case study from Castelluccio (Arezzo, central Italy)

International Nuclear Information System (INIS)

Venturi, Stefania; Vaselli, Orlando; Tassi, Franco; Nisi, Barbara; Pennisi, Maddalena; Cabassi, Jacopo; Bicocchi, Gabriele; Rossato, Luca

2015-01-01

In 2009 a deterioration of garden plants watered with domestic wells was related to high boron concentrations (up to 57 mg/L) measured in the shallow aquifer from the industrial area of Castelluccio (Tuscany, Italy), where several factories are or were using boron compounds for their industrial processes. Since 2012 a geochemical and isotopic survey of stream, ground and waste waters, and sediment samples was performed. In addition, monthly geochemical surveys were carried out from January to September 2013, during which concentrations of boron up to 139 mg/L were measured. The geochemical dataset also included raw (borax and sodium boron-hydride) and anthropogenic materials (B-rich slags and muds stored in one of the local factories), the latter being, to the best of our knowledge, analyzed for the first time in this work for bulk and leachate boron concentration and isotopic ratios. The results highlighted that the high concentrations of boron found in the local shallow aquifer had unequivocally an anthropogenic source. It was suggested that prolonged interaction between industrial (presently stored at ground level or buried) by-products and waste and meteoric waters was likely the main process responsible of the groundwater contamination as supported by the analysis of the major solutes. The dispersion of the contaminant could not clearly be observed downward the shallow hydrogeological circuit. Consequently, the presence of other sources of boron in the industrial area of Castelluccio cannot be excluded. This would also explain the reason why no univocal results were obtained by the "1"1B/"1"0B isotopic ratios measured in water, sediment and (bulk and leachate) anthropogenic samples. To minimize the boron contamination a hydraulic barrier should be constructed where the highest concentrations of boron were measured. - Highlights: • High boron concentrations were measured in a groundwater system near Arezzo (Italy). • Several factories in the local

Errors in instumental neutron activation analysis caused by matrix absorption

International Nuclear Information System (INIS)

Croudace, I.W.

1979-01-01

Instrumental neutron activation analysis of the geochemically important rare earth elements, together with Ta, Hf and U involves energies below 150 keV where absorption of radiation by the sample becomes inceasingly important. Determinations of the total mass absorption coefficients have been made. (C.F.)

Uruguay mining inventory. Geochemical prospecting results of the Las Flores aerial map[Study of Uranium geochemical prospection in Uruguay]; Inventario minero del Uruguay. Resultados de la prospeccion geoquimica del fotoplano Las Flores

Energy Technology Data Exchange (ETDEWEB)

Zeegers, H; Bonnefoy, D; Garau, M; Spangenberg, J

1981-07-01

In the context of the Uruguay mining inventory, the aerial photography map Las Flores had been covered by a specific strategic which included geochemical prospecting elements. The surface covered has the 550 km2, and 1042 samples which they have been analized in Orleans France. 22 elements by plasma spectroscopy and gold by atomic absorption and for uranium laser spectroscopy . They have been evidenced the following anomalies: gold, Pb, Pb-Ba-Cu, Ba and Ni-Cr.

An integrated geochemical, geophysical and mineralogical study of river sediments in alpine area and soil samples near steel plant, in Austria

Science.gov (United States)

Irfan, M. I.; Meisel, T.

2012-04-01

Concentration of nickel and chromium in any part of the ecosystem is important for environmental concerns in particular human health due to the reason that some species of them can cause health problem e.g. dermatitis and cancer. Sediment samples collected form a river Vordernberger Bach (Leoben, Austria) in an alpine region and soil samples collected in an area adjacent to steel production unit in same narrow valley were investigated. In previous studies a correlation between magnetic susceptibility values and concentration of nickel and chromium showed that a magnetic susceptibility meter can be used to point out the contaminated areas as in-situ device. The purpose of the whole study is to understand the real (point or diffuse, anthropogenic or geogenic) sources of contamination of soils, water and river sediments through heavy metal deposition. Unseparated, magnetic and non-magnetic fractions of soil samples were investigated for geochemical and mineralogical aspects with XRF, ICP-MS, EMPA, Multi-Functional Kappabridge (MFK1) and laser ablation coupled with ICP-MS. Mineralogical study of sediment samples for several sampling points with higher Ni and Cr content was performed. Sediment samples were sieved below 1.4 mm and then a concentrate of heavy minerals was prepared in the field through panning. Concentrated heavy minerals were then subjected for heavy liquid separation in the laboratory. Separated magnetic and non-magnetic fractions below 0.71/0.1 mm and density greater than 2.9 g/cm3 were selected for mineralogical investigation. The abundance of typical anthropogenic particles, e.g., spherical, tinder, roasted ores, iron and steel mill slag was observed under the microscope. Magnetite (mostly anthropogenic), maghemite, chromspinel, chromite (type I & II), (Ca,Al)-ferrite, wustite, apatite (anthropogenic), olivine mixed crystals, calcium silicate and spinel (anthropogenic) are found in magnetic fraction. Non-magnetic fractions contain hematite, siderite

Quantitative portable gamma spectroscopy sample analysis for non-standard sample geometries

International Nuclear Information System (INIS)

Enghauser, M.W.; Ebara, S.B.

1997-01-01

Utilizing a portable spectroscopy system, a quantitative method for analysis of samples containing a mixture of fission and activation products in nonstandard geometries was developed. The method can be used with various sample and shielding configurations where analysis on a laboratory based gamma spectroscopy system is impractical. The portable gamma spectroscopy method involves calibration of the detector and modeling of the sample and shielding to identify and quantify the radionuclides present in the sample. The method utilizes the intrinsic efficiency of the detector and the unattenuated gamma fluence rate at the detector surface per unit activity from the sample to calculate the nuclide activity and Minimum Detectable Activity (MDA). For a complex geometry, a computer code written for shielding applications (MICROSHIELD) is utilized to determine the unattenuated gamma fluence rate per unit activity at the detector surface. Lastly, the method is only applicable to nuclides which emit gamma rays and cannot be used for pure beta emitters. In addition, if sample self absorption and shielding is significant, the attenuation will result in high MDA's for nuclides which solely emit low energy gamma rays. The following presents the analysis technique and presents verification results demonstrating the accuracy of the method

Kriging - a challenge in geochemical mapping

Czech Academy of Sciences Publication Activity Database

Štojdl, J.; Matys Grygar, Tomáš; Elznicová, J.; Popelka, J.; Váchová, T.; Hošek, Michal

2017-01-01

Roč. 19, APR (2017) ISSN 1607-7962. [EGU General Assembly 2017. 23.04.2017-28.04.2017, Vienna] Institutional support: RVO:61388980 Keywords : kriging * geochemical mapping Subject RIV: DD - Geochemistry http://meetingorganizer.copernicus.org/EGU2017/EGU2017-3615.pdf

Geochemical modelling of groundwater evolution and residence time at the Kivetty site

Energy Technology Data Exchange (ETDEWEB)

Pitkaenen, P.; Luukkonen, A. [VTT Communities and Infrastructure, Espoo (Finland); Ruotsalainen, P. [Fintact Oy, Helsinki (Finland); Leino-Forsman, H.; Vuorinen, U. [VTT Chemical Technology, Espoo (Finland)

1998-12-01

An understanding of the geochemical evolution of groundwater is an essential part of the performance assessment and safety analysis of the final disposal of radioactive waste into the bedrock. The performance of technical barriers and migration of possibly released radionuclides depend on chemical conditions. A prerequisite for understanding these factors is the ability to specify the water-rock interactions which control chemical conditions in groundwater. The objective of this study is to interpret the processes and factors which control the hydrogeochemistry, such as pH and redox conditions. A model of the hydrogeochemical progress in different parts of the bedrock at Kivetty has been created and the significance of chemical reactions along different flowpaths calculated. Long term hydrodynamics have also been evaluated. The interpretation and modelling are based on groundwater samples (38 altogether) obtained from the soil layer, shallow wells in the bedrock, and five deep multi-packered boreholes (KRI-KR5) in the bedrock for which a comprehensive data set on dissolved chemical species and isotopes was available. Some analyses of dissolved gases and their isotopic measurements were also utilised. The data covers the bedrock at Kivetty to a depth of 850m. The results from groundwater chemistry, isotopes, petrography, hydrogeology of the site, geomicrobial studies, and PCA and speciation calculations were used in the evaluation of evolutionary processes at the site. The geochemical interpretation of water-rock interaction, isotope-chemical evolution and C-14 age calculations of groundwater was given a mass-balance approach (NETPATH). Reaction-path calculations (EQ3/6) were used to verify the thermodynamic feasibility of the reaction models obtained. The hydrogeochemistry of Kivetty is characterised by evolution from low-saline-carbonate-rich recharge water towards Na-Ca-Cl-type water. The salinity remains low. The most important changes in the chemistry of the

Geochemical modelling of groundwater evolution and residence time at the Kivetty site

International Nuclear Information System (INIS)

Pitkaenen, P.; Luukkonen, A.; Ruotsalainen, P.; Leino-Forsman, H.; Vuorinen, U.

1998-12-01

An understanding of the geochemical evolution of groundwater is an essential part of the performance assessment and safety analysis of the final disposal of radioactive waste into the bedrock. The performance of technical barriers and migration of possibly released radionuclides depend on chemical conditions. A prerequisite for understanding these factors is the ability to specify the water-rock interactions which control chemical conditions in groundwater. The objective of this study is to interpret the processes and factors which control the hydrogeochemistry, such as pH and redox conditions. A model of the hydrogeochemical progress in different parts of the bedrock at Kivetty has been created and the significance of chemical reactions along different flowpaths calculated. Long term hydrodynamics have also been evaluated. The interpretation and modelling are based on groundwater samples (38 altogether) obtained from the soil layer, shallow wells in the bedrock, and five deep multi-packered boreholes (KRI-KR5) in the bedrock for which a comprehensive data set on dissolved chemical species and isotopes was available. Some analyses of dissolved gases and their isotopic measurements were also utilised. The data covers the bedrock at Kivetty to a depth of 850m. The results from groundwater chemistry, isotopes, petrography, hydrogeology of the site, geomicrobial studies, and PCA and speciation calculations were used in the evaluation of evolutionary processes at the site. The geochemical interpretation of water-rock interaction, isotope-chemical evolution and C-14 age calculations of groundwater was given a mass-balance approach (NETPATH). Reaction-path calculations (EQ3/6) were used to verify the thermodynamic feasibility of the reaction models obtained. The hydrogeochemistry of Kivetty is characterised by evolution from low-saline-carbonate-rich recharge water towards Na-Ca-Cl-type water. The salinity remains low. The most important changes in the chemistry of the

Relative spatial soil geochemical variability along two transects across the United States and Canada

Science.gov (United States)

Garrett, Robert G.

2009-01-01

To support the development of protocols for the proposed North American Soil Geochemical Landscapes project, whose objective is to establish baselines for the geochemistry of North American soils, two continental-scale transects across the United States and Canada were sampled in 2004. The sampling employed a spatially stratified random sampling design in order to estimate the variability between 40-km linear sampling units, within them, at sample sites, and due to sample preparation and analytical chemical procedures. The 40-km scale was chosen to be consistent with the density proposed for the continental-scale project. The two transects, north–south (N–S) from northern Manitoba to the USA–Mexico border near El Paso, Texas, and east–west (E–W) from the Virginia shore north of Washington, DC, to north of San Francisco, California, closely following the 38th parallel, have been studied individually. The purpose of this study was to determine if statistically significant systematic spatial variation occurred along the transects. Data for 38 major, minor and trace elements in A- and C-horizon soils where less than 5% of the data were below the detection limit were investigated by Analysis of Variance (ANOVA). A total of 15 elements (K, Na, As, Ba, Be, Ce, La, Mn, Nb, P, Rb, Sb, Th, Tl and W) demonstrated statistically significant (p<0.05) variability at the between-40-km scale for both horizons along both transects. Only Cu failed to demonstrate significant variability at the between-40-km scale for both soil horizons along both transects.

Geochemical signature of columbite-tantalite and environmental impact of radioactive pegmatite mining in the Parelhas region, Rio Grande do Norte, Northeast Brazil

Energy Technology Data Exchange (ETDEWEB)

Moura, Jorge Costa de; Cruz, Paulo R.; Pereira, Valmir, E-mail: jcmoura@cnen.gov.br, E-mail: pcruz@cnen.gov.br, E-mail: vpereira@cnen.gov.br [Comissao Nacional de Energia Nuclear (CNEN-RJ), Rio de Janeiro, RJ (Brazil); Ludka, Isabel P.; Mendes, Julio C., E-mail: ludka@geologia.ufrj.br, E-mail: julio@geologia.ufrj.br [Universidade Federal de Rio do Janeiro (CCMN/UFRJ), Rio de Janeiro, RJ (Brazil). Centro de Ciencias Matematicas e da Natureza. Dept. de Geologia

2013-07-01

This article comprises geochemical, structural and radiometric investigations on radioactive pegmatites of the Borborema Pegmatitic Province in Northeast Brazil. The studied area is located in the surroundings of the city of Parelhas, in the geotectonic Province of Borborema. It is well known for its thousands of pegmatitic bodies exploited in primitive mines called garimpos. The main goal was to find an efficient, cheap and routine inspection procedure to identify the origin of commercialized radioactive columbite-tantalite (coltan) ore. The Brazilian Nuclear Energy Agency (CNEN) controls uranium commerce and nuclear activity in Brazil. Without an effective method to characterize coltan ores from different localities it is impossible to control the trade. The here presented new method was developed by correlating structural features of these pegmatites with the geochemical behavior of their coltan samples. It was found that the variation of U/Th vs. Nb{sub 2}O{sub 5}/Ta{sub 2}O{sub 5} provides geochemical signatures (analytical fingerprints) for the source location of such ore. The new method was tested with coltan samples of commercial batches from the Brazilian states of Amapa and Rondonia and also generated distinct geochemical signatures. A radiometric survey (CPS) to study the environmental impact of gamma radiation was also carried out in several mines and pegmatites. It included in situ measurements of pegmatite walls, enclosing rocks, soil, and accumulated water and revealed that gamma emitters are hardly solubilized and therefore environmental gamma radiation generally is not enhanced to a dangerous level. (author)

Status report on geochemical modelling

International Nuclear Information System (INIS)

Read, D.

1991-12-01

This report describes the findings of a review undertaken on behalf of the project management group of the programme 'Endlagersicherheit in der Nachbetriebsphase' based at GSF-IfT (Forschungszentrum fuer Umwelt und Gesundheit - Institut fuer Tieflagerung) to establish the current status of research into the simulation of geochemical processes relevant to radiological assessment. The review is intended to contribute to Stage 1 of a strategy formulated to enhance the use of geochemical models in Germany. Emphasis has been placed on processes deemed to be of greatest relevance to performance assessment for a HLW-repository in a salt dome principally, speciation-solubility in high salinity solutions, complexation by natural organics and generation-transport of colloids. For each of these and other topics covered, a summary is given of fundamental concepts, theoretical representations and their limitations, highlighting, where appropriate, the advantages and disadvantages of alternative approaches. The availability of data to quantify any given representation is addressed, taking into account the need for information at elevated temperatures and pressures. Mass transfer is considered in terms of aqueous, particulate and gas-mediated transport, respectively. (orig.) [de

NID Copper Sample Analysis

Energy Technology Data Exchange (ETDEWEB)

Kouzes, Richard T.; Zhu, Zihua

2011-09-12

The current focal point of the nuclear physics program at PNNL is the MAJORANA DEMONSTRATOR, and the follow-on Tonne-Scale experiment, a large array of ultra-low background high-purity germanium detectors, enriched in 76Ge, designed to search for zero-neutrino double-beta decay (0νββ). This experiment requires the use of germanium isotopically enriched in 76Ge. The MAJORANA DEMONSTRATOR is a DOE and NSF funded project with a major science impact. The DEMONSTRATOR will utilize 76Ge from Russia, but for the Tonne-Scale experiment it is hoped that an alternate technology, possibly one under development at Nonlinear Ion Dynamics (NID), will be a viable, US-based, lower-cost source of separated material. Samples of separated material from NID require analysis to determine the isotopic distribution and impurities. DOE is funding NID through an SBIR grant for development of their separation technology for application to the Tonne-Scale experiment. The Environmental Molecular Sciences facility (EMSL), a DOE user facility at PNNL, has the required mass spectroscopy instruments for making isotopic measurements that are essential to the quality assurance for the MAJORANA DEMONSTRATOR and for the development of the future separation technology required for the Tonne-Scale experiment. A sample of isotopically separated copper was provided by NID to PNNL in January 2011 for isotopic analysis as a test of the NID technology. The results of that analysis are reported here. A second sample of isotopically separated copper was provided by NID to PNNL in August 2011 for isotopic analysis as a test of the NID technology. The results of that analysis are also reported here.

Role of geochemical background at evaluation of investment attractiveness of recreational territories

Directory of Open Access Journals (Sweden)

Vdovina Ol'ga Konstantinovna

2014-09-01

Full Text Available The article shows the role of natural geochemical background when estimating investment attractiveness of recreational areas. It is noted, that geochemical background influence on people's sickness rate isn't considered now. Though it's understood, that even insignificant increase of geochemical background in relation to percentage abundance of Earth crest may lead to endemic diseases of people, animals and plants. An indicator of geochemical endemicity areas was proposed for assessing the impact of storage elements and of a lack of geological environment on human health. Thanks to this measure, and taking into account landscape features of the area, the authors allocated lands, dangerous and potentially dangerous in terms of endemicity. The importance of ratings was achieved by the use of those factors that could have a great influence on the cost of land development. This includes, first of all, the factors that affect population health, and economic and geographic factors that minimize the cost of the territory development and the factors that give rise to financial risks and risks of human losses. The main risk factors include: potential ecological and geochemical risk; high absolute heights, development and activity of dangerous geological processes and phenomena. Systemacity of researches was reached by using factors, that characterize the object from different aspects; readiness of area infrastructure to its exploration and possible risks. Objectivity was achieved by the use of figures obtained from the results of geochemical and engineering surveys with their metrological support.

Experimental study and numerical modelling of geochemical reactions occurring during uranium in situ recovery (ISR) mining

International Nuclear Information System (INIS)

Ben Simon, R.

2011-09-01

The in situ Recovery (ISR) method consists of ore mining by in situ chemical leaching with acid or alkaline solutions. ISR takes place underground and is therefore limited to the analysis of the pumped solutions, hence ISR mine management is still empirical. Numerical modelling has been considered to achieve more efficient management of this process. Three different phenomena have to be taken into account for numerical simulations of uranium ISR mining: (1) geochemical reactions; (2) the kinetics of these reactions, and (3) hydrodynamic transport with respect to the reaction kinetics. Leaching tests have been conducted on ore samples from an uranium mine in Tortkuduk (Kazakhstan) where ISR is conducted by acid leaching. Two types of leaching experiments were performed: (1) tests in batch reactors; and (2) extraction in flow through columns. The assumptions deduced from the leaching tests were tested and validated by modelling the laboratory experiments with the numerical codes CHESS and HYTEC, both developed at the Geosciences research center of Mines ParisTech. A well-constrained 1D hydrogeochemical transport model of the ISR process at laboratory-scale was proposed. It enables to translate the chemical release sequence that is observed during experiments into a geochemical reaction sequence. It was possible to highlight the controlling factors of uranium dissolution, and the precipitation of secondary mineral phase in the deposit, as well as the determination of the relative importance of these factors. (author)

Geochemical evidence for waning magmatism and polycyclic volcanism at Crater Flat, Nevada

International Nuclear Information System (INIS)

Perry, F.V.; Crowe, B.M.

1992-01-01

This paper reports that petrologic and geochemical studies of basaltic rocks in the Yucca Mountain region are currently focused on understanding the evolution of volcanism in the Crater Flat volcanic field and the mechanisms of polycyclic volcanic field and the mechanisms of polycyclic volcanism at the Lathrop Wells volcanic center, the youngest center in the Crater Flat volcanic field. Geochemical and petrologic data indicate that the magma chambers which supplied the volcanic centers at Crater Flat became situated at greater crustal depths as the field evolved. Deep magma chambers may be related to a waning magma flux that was unable to sustain upper crustal magma conduits and chambers. Geochemical data from the Lathrop Wells volcanic center indicate that eruptive units identified from field and geomorphic relationships are geochemically distinct. The geochemical variations cannot be explained by fractional crystallization of a single magma batch, indicating that several magma batches were involved in the formation of the Lathrop Wells center. Considering the low magma flux in the Yucca Mountain region in the Quaternary, the probability of several magma batches erupting essentially simultaneously at Lathrop Wells is considered remote

Spatial and Temporal Water Quality Dynamics in the Lake Maumelle Reservoir (Arkansas): Geochemical and Planktonic Variance in a Drinking Water Source

Science.gov (United States)

Carey, M. D.; Ruhl, L. S.

2017-12-01

The Lake Maumelle reservoir is Central Arkansas's main water supply. Maintaining a high standard of water quality is important to the over 400,000 residents of this area whom rely on this mesotrophic waterbody for drinking water. Lake Maumelle is also a scenic attraction for recreational boating and fishing. Past research has focused primarily on watershed management with land use/land cover modeling and quarterly water sampling of the 13.91mi2 reservoir. The surrounding land within the watershed is predominately densely forested, with timber farms and the Ouachita National Forest. This project identifies water quality changes spatially and temporally, which have not been as frequently observed, over a 6-month timespan. Water samples were collected vertically throughout the water column and horizontally throughout the lake following reservoir zonation. Parameters collected vertically for water quality profiles are temperature, dissolved oxygen, electrical conductivity, salinity, and pH. Soft sediment samples were collected and pore water was extracted by centrifuge. Cation and anion concentrations in the water samples were determined using ion chromatography, and trace element concentrations were determined using ICPMS. Planktonic abundances were determined using an inverted microscope and a 5ml counting chamber. Trace element, cation, and anion concentrations have been compared with planktonic abundance and location to determine microorganismal response to geochemical variance. During June 2017 sampling, parameters varied throughout the water column (temperature decreased 4 degrees Celsius and dissolved oxygen decreased from 98% to 30% from surface to bottom depths), revealing that the reservoir was becoming stratified. Collected plankton samples revealed the presence of copepod, daphnia, and dinoflagellate algae. Utricularia gibba was present in the littoral zone. Low electrical conductivity readings and high water clarity are consistent with the lake

Stepwise magnetic-geochemical approach for efficient assessment of heavy metal polluted sites

Science.gov (United States)

Appel, E.; Rösler, W.; Ojha, G.

2012-04-01

investment, a stepwise combined magnetic-geochemical site assessment leads to a clearly more significant characterization of soil pollution than by a common approach with exclusively random sampling for geochemical analysis, or alternatively to an equal quality result for lower costs.

Optimisation of beryllium-7 gamma analysis following BCR sequential extraction

International Nuclear Information System (INIS)

Taylor, A.; Blake, W.H.; Keith-Roach, M.J.

2012-01-01

Graphical abstract: Showing decrease in analytical uncertainty using the optimal (combined preconcentrated sample extract) method. nv (no value) where extract activities were 7 Be geochemical behaviour is required to support tracer studies. ► Sequential extraction with natural 7 Be returns high analytical uncertainties. ► Preconcentrating extracts from a large sample mass improved analytical uncertainty. ► This optimised method can be readily employed in studies using low activity samples. - Abstract: The application of cosmogenic 7 Be as a sediment tracer at the catchment-scale requires an understanding of its geochemical associations in soil to underpin the assumption of irreversible adsorption. Sequential extractions offer a readily accessible means of determining the associations of 7 Be with operationally defined soil phases. However, the subdivision of the low activity concentrations of fallout 7 Be in soils into geochemical fractions can introduce high gamma counting uncertainties. Extending analysis time significantly is not always an option for batches of samples, owing to the on-going decay of 7 Be (t 1/2 = 53.3 days). Here, three different methods of preparing and quantifying 7 Be extracted using the optimised BCR three-step scheme have been evaluated and compared with a focus on reducing analytical uncertainties. The optimal method involved carrying out the BCR extraction in triplicate, sub-sampling each set of triplicates for stable Be analysis before combining each set and coprecipitating the 7 Be with metal oxyhydroxides to produce a thin source for gamma analysis. This method was applied to BCR extractions of natural 7 Be in four agricultural soils. The approach gave good counting statistics from a 24 h analysis period (∼10% (2σ) where extract activity >40% of total activity) and generated statistically useful sequential extraction profiles. Total recoveries of 7 Be fell between 84 and 112%. The stable Be data demonstrated that the

Oak Ridge Geochemical Reconnaissance Program

International Nuclear Information System (INIS)

Arendt, J.W.

1977-03-01

The Oak Ridge reconnaissance program is responsible for the geochemical survey in a 12-state area covering Texas, Oklahoma, Kansas, Nebraska, South Dakota, North Dakota, Minnesota, Wisconsin, Michigan, Iowa, Indiana, and Illinois as part of the National Uranium Resource Evaluation Program. The program concept is outlined and the planning and organization of the program is discussed

The effects of sorting by aeolian processes on the geochemical characteristics of surface materials: a wind tunnel experiment

Science.gov (United States)

Wang, Xunming; Lang, Lili; Hua, Ting; Zhang, Caixia; Li, Hui

2018-03-01

The geochemical characteristics of aeolian and surface materials in potential source areas of dust are frequently employed in environmental reconstructions as proxies of past climate and as source tracers of aeolian sediments deposited in downwind areas. However, variations in the geochemical characteristics of these aeolian deposits that result from near-surface winds are currently poorly understood. In this study, we collected surface samples from the Ala Shan Plateau (a major potential dust source area in Central Asia) to determine the influence of aeolian processes on the geochemical characteristics of aeolian transported materials. Correlation analyses show that compared with surface materials, the elements in transported materials (e.g., Cu, As, Pb, Mn, Zn, Al, Ca, Fe, Ga, K, Mg, P, Rb, Co, Cr, Na, Nb, Si, and Zr) were subjected to significant sorting by aeolian processes, and the sorting also varied among different particle size fractions and elements. Variations in wind velocity were significantly correlated with the contents of Cr, Ga, Sr, Ca, Y, Nd, Zr, Nb, Ba, and Al, and with the Zr/Al, Zr/Rb, K/Ca, Sr/Ca, Rb/Sr, and Ca/Al ratios. Given the great variation in the geochemical characteristics of materials transported under different aeolian processes relative to those of the source materials, these results indicate that considerable uncertainty may be introduced to analyses by using surface materials to trace the potential source areas of aeolian deposits that accumulate in downwind areas.

Top Soils Geochemical and Radioactivity Survey of Naples (Italy) Metropolitan.

Science.gov (United States)

Somma, R.; De Vivo, B.; Cicchella, D.

2001-05-01

The metropolitan area of Naples due to intense human activities is an emblematic area affected by various environmental pollution of soils and waters in addition to hydrogeological volcanic, seismic and bradyseismic hazards. The geology of the area is prevailing represented by volcanics erupted, from the Upper Pleistocene to Recent by Mt. Somma-Vesuvius on the east and the Campi Flegrei fields on the west. The morphology of the metropolitan area of Naples city can be subdivided in flat areas, constituted by reworked pyroclastic terrains, and by hills originated by the overlapping of different welded pyroclastic flows (i.e.: Campanian Ignimbrite and Neapoletan Yellow Tuff) intercalated with pyroclastic deposits of different origins (i.e.: Campi Flegrei, Mt. Somma-Vesuvius, Ischia) and ages. In order to compile a multi-element baseline geochemical and radioactivity mapping of the metropolitan area of the Napoli we have sampled for this study, in situ top soil and imported filling material (mainly soil, volcanic ash, pumice and scoriae). The sampling and radioactivity survey has been carried out on about 200 sampling sites covering an area of about 150 Km2, with a grid of 0.5 x 0.5 km in the urbanised downtown and 1 km x 1 km in the sub urban areas. In each site has been determined a radioactivity by a Scintrex GRS-500 at different emission spectra as total radioactivity (> 0.08 MeV and > 0.40 MeV), 238U (at 1.76 MeV mostly from 214Bi), 232Th (at 2.6 MeV mostly from 208Tl) and 40K (at 1.46 MeV mostly for 40K). The range of values of in situ soils are as follow for the in situ soils (Total radioactivity: 1327- 360 and 114- 47; 238U: 2.6- 1.3; 40K: 8.1- 3.1; 232U: 0.5- 0.1). Analyses of major, metallic elements and pH of each soil sample are in progress, while Pb isotopes compositions, for a selected number of samples, will be determined to discriminate the natural (geogenic) from the anthropogenic components in the soils by versus the anthropogenetic origin. The data

Preliminary delineation of natural geochemical reactions, Snake River Plain aquifer system, Idaho National Engineering Laboratory and vicinity, Idaho

International Nuclear Information System (INIS)

Knobel, L.L.; Bartholomay, R.C.; Orr, B.R.

1997-05-01

The U.S. Geological Survey, in cooperation with the U.S. Department of Energy, is conducting a study to determine the natural geochemistry of the Snake River Plain aquifer system at the Idaho National Engineering Laboratory (INEL), Idaho. As part of this study, a group of geochemical reactions that partially control the natural chemistry of ground water at the INEL were identified. Mineralogy of the aquifer matrix was determined using X-ray diffraction and thin-section analysis and theoretical stabilities of the minerals were used to identify potential solid-phase reactants and products of the reactions. The reactants and products that have an important contribution to the natural geochemistry include labradorite, olivine, pyroxene, smectite, calcite, ferric oxyhydroxide, and several silica phases. To further identify the reactions, analyses of 22 representative water samples from sites tapping the Snake River Plain aquifer system were used to determine the thermodynamic condition of the ground water relative to the minerals in the framework of the aquifer system. Principal reactions modifying the natural geochemical system include congruent dissolution of olivine, diopside, amorphous silica, and anhydrite; incongruent dissolution of labradorite with calcium montmorillonite as a residual product; precipitation of calcite and ferric oxyhydroxide; and oxidation of ferrous iron to ferric iron. Cation exchange reactions retard the downward movement of heavy, multivalent waste constituents where infiltration ponds are used for waste disposal

Manual for the sampling of uranium mine tailings

International Nuclear Information System (INIS)

Feenstra, S.; Reades, D.W.; Cherry, J.A.; Chambers, D.B.; Case, G.G.; Ibbotson, B.G.

1983-04-01

The purpose of this manual is to describe the requisite sampling procedures to provide a basis for the application of uniform high-quality standards to detailed geotechnical, hydrogeological, geochemical and air quality measurements at Canadian uranium tailings disposal sites. The report describes the objective and scope of a sampling program, the preliminary data collection, and the procedures for sampling of tailings solids, surface water and seepage, tailings porewater, and wind-blown dust and radon

Modeling of geochemical processes in the submarine discharge zone of hydrothermal solutions

Directory of Open Access Journals (Sweden)

С. М. Судариков

2017-06-01

Full Text Available The paper reviews the main methods and analyzes modeling results for geochemical processes in the submarine discharge zone of hydrothermal solutions of mid-ocean ridges. Initial data for modeling have been obtained during several marine expeditions, including Russian-French expedition SERPENTINE on the research vessel «Pourquoi Рas?» (2007. Results of field observations, laboratory experiments and theoretical developments are supported by the analysis of regression model of mixing between hydrothermal solutions and sea water. Verification of the model has been carried out and the quality of chemical analysis has been assessed; degree and character of participation of solution components in the hydrothermal process have been defined; the content of end members has been calculated basing on reverse forecasting of element concentration, depending on regression character; data for thermodynamic modeling have been prepared. Regression model of acid-base properties and chloridity of mineralizing thermal springs confirms adequacy of the model of double-diffusive convection for forming the composition of hydrothermal solutions.  Differentiation of solutions according to concentrations of chloride-ion, depending on temperature and pH indicator within this model, is associated with phase conversions and mixing of fluids from two convection cells, one of which is a zone of brine circulation. In order to carry out computer thermodynamic modeling, hydro-geochemical and physicochemical models of hydrothermal discharge zone have been created. Verification of the model has been carried out basing on changes of Mn concentration in the hydrothermal plume. Prevailing forms of Mn migration in the plume are Mn2+, MnCl+, MnCl2. Two zones have been identified in the geochemical structure of the plume: 1 high-temperature zone (350-100 °С with prevalence of chloride complexes – ascending plume; 2 low-temperature zone (100-2 °С, where predominant form of

Maceral and geochemical characteristics of oil shale 2 from the Huangxian Basin, China

Energy Technology Data Exchange (ETDEWEB)

Sun, Yuzhuang; Lin, Mingyue; Li, Haimei; Zhang, Hongjian; Li, Shifeng; Jin, Kankun [Hebei Architectural Science and Technology Inst., Handan, Hebei (China)

2001-07-01

Five samples of Oil Shale 2 from the Huangxian Basin have been analysed by coal petrographic and geochemical methods in order to study its formation environment. Higher alginite ratios and hopanes in Oil Shale 2 indicate a lower plants and anoxic environment. Two ternary diagrams of 'facies diagnostic' macerals and biomarkers were used to interpret the depositional environments of organic matter in Oil Shale 2. In both diagrams, Oil Shale 2 plots in a lower plant zone, and was deposited in a deeper water environment. (Author)

Geochemical evolution of highly alkaline and saline tank waste plumes during seepage through vadose zone sediments

International Nuclear Information System (INIS)

Wan, Jiamin; Tokunaga, Tetsu K.; Larsen, Joern T.; Serne, R. JEFFREY

2004-01-01

Leakage of highly saline and alkaline radioactive waste from storage tanks into underlying sediments is a serious environmental problem at the Hanford Site in Washington State. This study focuses on geochemical evolution of tank waste plumes resulting from interactions between the waste solution and sediment. A synthetic tank waste solution was infused into unsaturated Hanford sediment columns (0.2, 0.6, and 2 m) maintained at 70C to simulate the field contamination process. Spatially and temporally resolved geochemical profiles of the waste plume were obtained. Thorough OH neutralization (from an initial pH 14 down to 6.3) was observed. Three broad zones of pore solutions were identified to categorize the dominant geochemical reactions: the silicate dissolution zone (pH > 10), pH-neutralized zone (pH 10 to 6.5), and displaced native sediment pore water (pH 6.5 to 8). Elevated concentrations of Si, Fe, and K in plume fluids and their depleted concentrations in plume sediments reflected dissolution of primary minerals within the silicate dissolution zone. The very high Na concentrations in the waste solution resulted in rapid and complete cation exchange, reflected in high concentrations of Ca and Mg at the plume front. The plume-sediment profiles also showed deposition of hydrated solids and carbonates. Fair correspondence was obtained between these results and analyses of field borehole samples from a waste plume at the Hanford Site. Results of this study provide a well-defined framework for understanding waste plumes in the more complex field setting and for understanding geochemical factors controlling transport of contaminant species carried in waste solutions that leaked from single-shell storage tanks in the past

Uranium-233 analysis of biological samples

International Nuclear Information System (INIS)

Gies, R.A.; Ballou, J.E.; Case, A.C.

1979-01-01

Two liquid scintillation techniques were compared for 233 U analysis: a two-phase extraction system (D2EHPA) developed by Keough and Powers, 1970, for Pu analysis; and a single-phase emulsion system (TT21) that holds the total sample in suspension with the scintillator. The first system (D2EHPA) was superior in reducing background (two- to threefold) and in accommodating a larger sample volume (fivefold). Samples containing > 50 mg/ml of slats were not extracted quantitatively by D2EHPA

Magnetic and Geochemical Properties of Andic Soils from the Massif Central, France

Science.gov (United States)

Grison, H.; Petrovsky, E.; Dlouha, S.; Kapicka, A.

2014-12-01

Ferrimagnetic iron oxides are the key magnetic minerals responsible for enhancement of the magnetic susceptibility in soils. Soils with andic properties contain high amount of Fe-oxides, but only few attempts were made to characterize these soils using magnetic methods. Magnetic susceptibility is in particular suitable for its sensitivity and fast measurement; the presence of Fe-oxides can be easily identified directly in the field. The aim of our study is to describe main magnetic and geochemical properties of soils rich in Fe oxides derived from strongly magnetic volcanic basement. The studied sites are located at the basalt parent rock formed during Pleistocene, Pliocene and Miocene. Investigated soils are exposed to the mountainous climate with the perudic soil moisture regime and cryic temperature soil regime. Seven basalt soil profiles with typical andic properties were analyzed down to parent rock by a set of magnetic and geochemical methods. The magnetic susceptibility was measured in situ and in laboratory using the Bartington MS2D and AGICO MFK1. Its temperature dependence was measured in order to assess phase transformations of magnetic minerals using the KLY4. Magnetic data were completed by the hysteresis, IRM and DCD measurements using ADE EV9 VSM. Geochemical data include soil reaction (pH), organic carbon, cations exchange capacity, and extractable iron and aluminium in the soil extracted by a dithionite-citrate, acid-ammonium oxalate and a pyrophosphate solution. Scanning electron microscopy was done for top/sub-soil and rock samples. Geochemical soil properties reflecting iron oxide stability correlate well with mass-specific magnetic susceptibility. Well pronounced relationship was observed between magnetic grain size, precipitation and soil pH, second group is reflecting concentration of feri-magnetic particles and age of parent rock, and the third group reflects degree of weathering and the thermomagnetic indices expressing changes in magneto

Exomars 2018 Rover Pasteur Payload Sample Analysis

Science.gov (United States)

Debus, Andre; Bacher, M.; Ball, A.; Barcos, O.; Bethge, B.; Gaubert, F.; Haldemann, A.; Kminek, G.; Lindner, R.; Pacros, A.; Rohr, T.; Trautner, R.; Vago, J.

The ExoMars programme is a joint ESA-NASA program having exobiology as one of the key science objectives. It is divided into 2 missions: the first mission is ESA-led with an ESA orbiter and an ESA Entry, Descent and Landing (EDL) demonstrator, launched in 2016 by NASA, and the second mission is NASA-led, launched in 2018 by NASA including an ESA rover and a NASA rover both deployed by a single NASA EDL system. For ESA, the ExoMars programme will demonstrate key flight and in situ enabling technologies in support of the European ambitions for future exploration missions, as outlined in the Aurora Declaration. The ExoMars 2018 ESA Rover will carry a comprehensive and coherent suite of analytical instruments dedicated to exobiology and geology research: the Pasteur Payload (PPL). This payload includes a selection of complementary instruments, having the following goals: to search for signs of past and present life on Mars and to investigate the water/geochemical environment as a function of depth in the shallow subsurface. The ExoMars Rover will travel several kilometres searching for sites warranting further investigation. The Rover includes a drill and a Sample Preparation and Distribution System which will be used to collect and analyse samples from within outcrops and from the subsurface. The Rover systems and instruments, in particular those located inside the Analytical Laboratory Drawer must meet many stringent requirements to be compatible with exobiologic investigations: the samples must be maintained in a cold and uncontaminated environment, requiring sterile and ultraclean preparation of the instruments, to preserve volatile materials and to avoid false positive results. The value of the coordinated observations suggests that a significant return on investment is to be expected from this complex development. We will present the challenges facing the ExoMars PPL, and the plans for sending a robust exobiology laboratory to Mars in 2018.

Study of the coupling of geochemical models based on thermodynamic equilibrium with models of component transfer as solutions in porous media or fractures

International Nuclear Information System (INIS)

Coudrain-Ribstein, A.

1985-01-01

This study is a contribution of analyses possibilities of modelling the transfer of components in the underground taking into account complexes geochemical phenomena. In the first part, the aim and the methodology of existing codes are presented. The transfer codes describe with a great precision the physical phenomena of transport but they are based on a very simple conceptualisation of the geochemical phenomena of retention by the rock. The geochemical models are interested by a stable unity of volume. They allow to compute the equilibrium distribution of the components between the chemical species of the solution, and the solid and gaseous phases. They use important thermodynamic data bases corresponding to each possible reaction. To sum up the situation about the geochemical codes in Europe and United States, a list of about thirty codes describe their method and potentialities. The mathematical analysis of the different methods used in both types of codes is presented. Then, the principles of a modelisation associating the potentialities of the transport codes and the geochemical codes are discussed. It is not possible to think of a simple coupling. A general code must be established on the bases of the existing codes but also on new concepts and under new constraints. In such studies one must always deal with the problem of the reactions kinetics. When the velocity of the reactions is big enough versus the velocity of transport processes, the assumption of local geochemical equilibrium can be retained. A general code would be very cumbersome, expensive and difficult to use. The results would be difficult to analyse and exploit. On the other hand, for each case study, a detailed analysis can point out many computing simplifications without simplifying the concepts [fr

Rare Earth Elements (La, Ce, Pr, Nd, and Sm from a Carbonatite Deposit: Mineralogical Characterization and Geochemical Behavior

Directory of Open Access Journals (Sweden)

Mohamed Edahbi

2018-02-01

Full Text Available Geochemical characterization including mineralogical measurements and kinetic testing was completed on samples from the Montviel carbonatite deposit, located in Quebec (Canada. Three main lithological units representing both waste and ore grades were sampled from drill core. A rare earth element (REE concentrate was produced through a combination of gravity and magnetic separation. All samples were characterized using different mineralogical techniques (i.e., quantitative evaluation of minerals by scanning electron microscopy (QEMSCAN, X-ray diffraction (XRD, and scanning electron microscopy with X-ray microanalysis (SEM-EDS in order to quantify modal mineralogy, liberation, REE deportment and composition of REE-bearing phases. The REE concentrate was then submitted for kinetic testing (weathering cell in order to investigate the REE leaching potential. The mineralogical results indicate that: (i the main REE-bearing minerals in all samples are burbankite, kukharenkoite-Ce, monazite, and apatite; (ii the samples are dominated by REE-free carbonates (i.e., calcite, ankerite, and siderite; and (iii LREE is more abundant than HREE. Grades of REE minerals, sulfides and oxides are richer in the concentrate than in the host lithologies. The geochemical test results show that low concentrations of light REE are leached under kinetic testing conditions (8.8–139.6 µg/L total light REE. These results are explained by a low reactivity of the REE-bearing carbonates in the kinetic testing conditions, low amounts of REE in solids, and by precipitation of secondary REE minerals.

Diffuse Volcanism at the Young End of the Walvis Ridge - Tristan - Gough Seamount Province: Geochemical Sampling and Constraints on Plume Dynamics

Science.gov (United States)

Class, C.; Koppers, A. A. P.; Sager, W. W.; Schnur, S.

2014-12-01

The Walvis Ridge-Tristan/Gough seamount province in the South Atlantic represents 130 Myr of continuous intra-plate volcanism that can be connected to the once conjunct Parana-Etendeka flood basalt province. With this it represents one of the few primary hotspots consistent with the thermal plume model. However, around 60 Ma, the morphological expression of the Walvis Ridge changed drastically from a robust 200 km wide aseismic ridge into a 400 km wide region of diffuse and diminished volcanism. As a result, this part of the plume trail has been described by two subtracks, one ending at Tristan da Cunha and another at Gough Island more than 400 km to the SSE. Where the Walvis Ridge forks into these two tracks there is a center prong. There is also the 39.5°S lineament of seamounts between, but oblique to, the two subtracks, which is parallel to the local fracture zone directions. All these features are at odds with the classical definition of a narrow hotspot track although Rohde et al. (2013) showed that the Tristan and Gough subtracks retain a distinct geochemical signature over 70 Myr and are consistent with a zoned, deep-seated plume. The first Sr-Nd-Hf-Pb isotopic and trace element analyses from the detailed dredge sampling cruise MV1203 show that samples from two prominent seamounts at the western end of the 39.5°S lineament have a Gough-type signature, which makes an upper mantle source for this lineament unlikely but rather indicates that the Gough-type source stretches some 200 km NNW from Gough. Tristan track seamount samples are comparable with published data, however, one new sample has a Gough-type composition suggesting leakage of this component into the Tristan-type plume zone. Seamounts on the middle prong of the Walvis Ridge fork have compositions intermediate to Gough and Tristan domains, suggesting mixing between sources or melts of the two domains. Thus, the Gough-component in the last 60 Myr of plume activity is volumetrically much more

Geochemical characterisation of Elbe river high flood sediments

Energy Technology Data Exchange (ETDEWEB)

Krueger, F. [UFZ - Umweltforschungszentrum Leipzig-Halle GmbH, Falkenberg (Germany). Sektion Boden-/Gewaesserforschung]|[UFZ - Umweltforschungszentrum Leipzig-Halle GmbH, Magdeburg (Germany). Sektion Gewaesserforschung; Rupp, H.; Meissner, R. [UFZ - Umweltforschungszentrum Leipzig-Halle GmbH, Falkenberg (Germany). Sektion Boden-/Gewaesserforschung; Lohse, M.; Buettner, O.; Friese, K. [UFZ - Umweltforschungszentrum Leipzig-Halle GmbH, Magdeburg (Germany). Sektion Gewaesserforschung; Miehlich, G. [Hamburg Univ. (Germany). Inst. fuer Bodenkunde

2001-07-01

Quality aims for land usage in flood plains have to be worked out in the Russian-German research project 'Effects of floods on the pollution of agricultural used flood plain soils of the Oka River and the Elbe River'. It is financed by the Germany Ministry of Education and Research (FKZ 02 WT 9617/0). Beside the characterisation of the present pollution of soils for the middle Elbe, it is necessary to prognosticate the current pollutant input. At the examination site nearby Wittenberge, Elbe River kilometers 435 and 440, natural deposited flood sediments were sampled by artificial lawn mats. By the geochemical characterisation it is possible to record the metal input into the flood plain and to win knowledge about the sedimentation process. The results of sediment investigation of the high flood in spring 1997 are presented. (orig.)

Influence of sampling depth and post-sampling analysis time on the ...

African Journals Online (AJOL)

Bacteriological analysis was carried out for samples taken at water depth and at 1, 6, 12 and 24 hours post-sampling. It was observed that the total and faecal coliform bacteria were significantly higher in the 3 m water depth samples than in the surface water samples (ANOVA, F = 59.41, 26.751, 9.82 (T.C); 46.41, 26.81, ...

Geochemical methods for identification of formations being prospective for uranium

International Nuclear Information System (INIS)

Zhukova, A.M.; Komarova, N.I.; Spiridonov, A.A.; Shor, G.M.

1985-01-01

Geochemical methods of uranium content evaluation in metamorphic, ultrametamorphic and sedimentary formations are considered. At that, the following four factors are of the highest importance: 1) average uranium content-geochemical background; 2) character of uranium distribution; 3) forms of uranium presence; 4) the value of thorium-uranium ratio. A complex of radiogeochemical criteria, favourable for uranium presence is formulated: high average background content of total and '' mobile''uranium and high value of variation coefficient (80-100% and above); low (approximately one or lower) thorium-uranium ratio; sharp increase in uranium concentration in accessory minerals. Radiogeochemical peculiarities of metamorphic and ultrametamorphic formations prospective for uranium are enumerated. The peculiarities condition specificity of geochemical prospecting methods. Prospecting methods first of all must be directed at the evaluation of radioelement distribution parameters and specification of the forms of their presence

Geochemical Data Package for Performance Assessment Calculations Related to the Savannah River Site

Energy Technology Data Exchange (ETDEWEB)

Kaplan, Daniel I. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2016-07-22

The Savannah River Site (SRS) disposes of low-level radioactive waste (LLW) and stabilizes high-level radioactive waste (HLW) tanks in the subsurface environment. Calculations used to establish the radiological limits of these facilities are referred to as Performance Assessments (PA), Special Analyses (SA), and Composite Analyses (CA). The objective of this document is to revise existing geochemical input values used for these calculations. This work builds on earlier compilations of geochemical data (2007, 2010), referred to a geochemical data packages. This work is being conducted as part of the on-going maintenance program of the SRS PA programs that periodically updates calculations and data packages when new information becomes available. Because application of values without full understanding of their original purpose may lead to misuse, this document also provides the geochemical conceptual model, the approach used for selecting the values, the justification for selecting data, and the assumptions made to assure that the conceptual and numerical geochemical models are reasonably conservative (i.e., bias the recommended input values to reflect conditions that will tend to predict the maximum risk to the hypothetical recipient). This document provides 1088 input parameters for geochemical parameters describing transport processes for 64 elements (>740 radioisotopes) potentially occurring within eight subsurface disposal or tank closure areas: Slit Trenches (ST), Engineered Trenches (ET), Low Activity Waste Vault (LAWV), Intermediate Level (ILV) Vaults, Naval Reactor Component Disposal Areas (NRCDA), Components-in-Grout (CIG) Trenches, Saltstone Facility, and Closed Liquid Waste Tanks. The geochemical parameters described here are the distribution coefficient, Kd value, apparent solubility concentration, k_s value, and the cementitious leachate impact factor.

Geochemical and mineralogical study of selected weathered samples from Olkiluoto site

International Nuclear Information System (INIS)

Lindberg, A.

2009-02-01

Optical microscopy, chemical analyses and X-ray diffraction method were used to study the influence of weathering from 11 drill core samples from shallow depths (< 25 m). The samples, 4 to 22 cm in length were drilled from Olkiluoto study site, Eurajoki, and they represent the common rock types of local bedrock: mica gneiss, tonalitic and granodioritic gneiss. Two of the samples were macroscopically unweathered and 9 of them were remarkably altered. The alteration was shown as porosity, the abundance of chlorite instead of biotite and pink, unclear feldspars. Many samples also contained red-brown hematite and fractures, some of them coated with secondary minerals, even clay. Microscopically the most visible feature of weathering was the total alteration of plagioclase and cordierite to sericite. In many samples also biotite was richly altered to chlorite and opaque minerals. Microfractures were common and they were filled by hematite, kaolinite and fine-grained muscovite (sericite). Hematite was, in some cases, also largely replacing the weathered minerals, feldspars and cordierite. Chemical alteration was not clear, because the alteration of main minerals have produced secondary minerals with almost the same chemical composition without any reasonable depleting or enrichment of certain elements. X-ray diffraction determination of samples proved, that often plagioclase was replaced by mica and biotite by chlorite. In some cases the samples contained products of chemical weathering, kaolinite and smectite. (orig.)

Geochemical fingerprints and pebbles zircon geochronology

Indian Academy of Sciences (India)

Home; Journals; Journal of Earth System Science; Volume 125; Issue 7. Geochemical fingerprints and pebbles zircon geochronology: Implications for the provenance and tectonic setting of Lower Cretaceous sediments in the Zhucheng Basin (Jiaodong peninsula, North China). Jin-Long Ni Jun-Lai Liu Xiao-Ling Tang ...

Enhanced AFCI Sampling, Analysis, and Safeguards Technology Review

Energy Technology Data Exchange (ETDEWEB)

John Svoboda

2009-09-01

The focus of this study includes the investigation of sampling technologies used in industry and their potential application to nuclear fuel processing. The goal is to identify innovative sampling methods using state of the art techniques that could evolve into the next generation sampling and analysis system for metallic elements. Sampling and analysis of nuclear fuel recycling plant processes is required both to monitor the operations and ensure Safeguards and Security goals are met. In addition, environmental regulations lead to additional samples and analysis to meet licensing requirements. The volume of samples taken by conventional means, can restrain productivity while results samples are analyzed, require process holding tanks that are sized to meet analytical issues rather than process issues (and that create a larger facility footprint), or, in some cases, simply overwhelm analytical laboratory capabilities. These issues only grow when process flowsheets propose new separations systems and new byproduct material for transmutation purposes. Novel means of streamlining both sampling and analysis are being evaluated to increase the efficiency while meeting all requirements for information. This report addresses just a part of the effort to develop and study novel methods by focusing on the sampling and analysis of aqueous samples for metallic elements. It presents an overview of the sampling requirements, including frequency, sensitivity, accuracy, and programmatic drivers, to demonstrate the magnitude of the task. The sampling and analysis system needed for metallic element measurements is then discussed, and novel options being applied to other industrial analytical needs are presented. Inductively coupled mass spectrometry instruments are the most versatile for metallic element analyses and are thus chosen as the focus for the study. Candidate novel means of process sampling, as well as modifications that are necessary to couple such instruments to

Geochemical, hydrological, and biological cycling of energy residual. Research plan

International Nuclear Information System (INIS)

Wobber, F.J.

1983-03-01

Proposed research goals and specific research areas designed to provide a base of fundamental scientific information so that the geochemical, hydrological, and biophysical mechanisms that contribute to the transport and long term fate of energy residuals in natural systems can be understood are described. Energy development and production have resulted in a need for advanced scientific information on the geochemical transformations, transport rates, and potential for bioaccumulation of contaminants in subsurface environments

Sample collection and sample analysis plan in support of the 105-C/190-C concrete and soil sampling activities

International Nuclear Information System (INIS)

Marske, S.G.

1996-07-01

This sampling and analysis plan describes the sample collection and sample analysis in support of the 105-C water tunnels and 190-C main pumphouse concrete and soil sampling activities. These analytical data will be used to identify the radiological contamination and presence of hazardous materials to support the decontamination and disposal activities

Determination of thorium in seawater by neutron activation analysis and mass spectrometry

International Nuclear Information System (INIS)

Huh, Chih-An.

1987-01-01

The recent development of neutron activation analysis and mass spectrometric methods for the determination of 232 Th in seawater has made possible rapid sampling and analysis of this long-lived, non-radiogenic thorium isotope on small-volume samples. The marine geochemical utility of 232 Th, whose concentration in seawater is extremely low, warrants the development of these sensitive techniques. The analytical methods and some results are presented and discussed in this article. 24 refs., 3 figs

Radiochemical analysis of phosphorus in milk samples

International Nuclear Information System (INIS)

Oliveira, R.M. de; Cunha, I.I.L.

1991-01-01

The determination of phosphorus in milk samples by thermal neutron activation analysis employing radiochemical separation is described. The radiochemical separation consists of the simultaneous irradiation of samples and standards, dissolution of the milk samples in a perchloric acid and nitric acid mixture, addition of zinc hold-back carrier, precipitation of phosphorus as ammonium phospho molybdate (A.M.P.) and sample counting in a Geiger-Mueller detector. The analysis sources of error were studied and the established method was applied to phosphorus analyses in commercial milk samples. (author)

Adaptive Multiscale Modeling of Geochemical Impacts on Fracture Evolution

Science.gov (United States)

Molins, S.; Trebotich, D.; Steefel, C. I.; Deng, H.

2016-12-01

Understanding fracture evolution is essential for many subsurface energy applications, including subsurface storage, shale gas production, fracking, CO2 sequestration, and geothermal energy extraction. Geochemical processes in particular play a significant role in the evolution of fractures through dissolution-driven widening, fines migration, and/or fracture sealing due to precipitation. One obstacle to understanding and exploiting geochemical fracture evolution is that it is a multiscale process. However, current geochemical modeling of fractures cannot capture this multi-scale nature of geochemical and mechanical impacts on fracture evolution, and is limited to either a continuum or pore-scale representation. Conventional continuum-scale models treat fractures as preferential flow paths, with their permeability evolving as a function (often, a cubic law) of the fracture aperture. This approach has the limitation that it oversimplifies flow within the fracture in its omission of pore scale effects while also assuming well-mixed conditions. More recently, pore-scale models along with advanced characterization techniques have allowed for accurate simulations of flow and reactive transport within the pore space (Molins et al., 2014, 2015). However, these models, even with high performance computing, are currently limited in their ability to treat tractable domain sizes (Steefel et al., 2013). Thus, there is a critical need to develop an adaptive modeling capability that can account for separate properties and processes, emergent and otherwise, in the fracture and the rock matrix at different spatial scales. Here we present an adaptive modeling capability that treats geochemical impacts on fracture evolution within a single multiscale framework. Model development makes use of the high performance simulation capability, Chombo-Crunch, leveraged by high resolution characterization and experiments. The modeling framework is based on the adaptive capability in Chombo

Multielemental analysis of milk samples

International Nuclear Information System (INIS)

Omar Al-Dayel; Jameel Al-Hefne; Didarul A Chowdhury; Turki Al-Ajyan

2002-01-01

Milk is a basic food since it provides essential nutrients (proteins, lipids, carbohydrates) and micronutrients (minerals, Vitamins, enzymes). In fact, in formula milk essential elements have been usually added in order to satisfy nutritional requirements. However, too high additions of these elements can produce detrimental effects on human health. More important, milk can also constitute a source of exposure to toxic elements, especially dangerous for infants. Method is presented for the multielemental analysis of a wide range of elements in milk samples. The aim of this work is the development of a multielemental method for the analysis of major, minor and trace essential and toxic elements in milk. Several milk samples with different origins were collected from the Saudi Arabia markets and analyzed by Inductively Coupled Plasma Mass Spectrometer (ICP-MS). For preparation of the samples for analysis, they were digested by closed vessel microwave digestion system with H 2 O 2 /HNO 3 . About 40 elements were determined. A reference material was analysed for the validation of the proposed method. (Author)

Geochemical model of a geothermal system: an approach on the analytical uncertainty; Modelo geoquimico de sistema geotermico: un enfoque sobre la incertidumbre analitica

Energy Technology Data Exchange (ETDEWEB)

Pal Verma, Mahendra [Instituto de Investigaciones Electricas, Cuernavaca, Morelos (Mexico)

2008-07-01

A procedure was developed to consider the analytical uncertainty in each parameter of geochemical analysis of geothermal fluid. The estimation of the uncertainty is based on the results of the geochemical analyses of geothermal fluids (numbered from the 0 to the 14), obtained within the framework of the comparisons program among the geochemical laboratories in the last 30 years. Also the propagation of the analytical uncertainty was realized in the calculation of the parameters of the geothermal fluid in the reservoir, through the methods of interval of uncertainty and GUM (Guide to the expression of Uncertainty of Measurement). The application of the methods is illustrated in the pH calculation of the geothermal fluid in the reservoir, considering samples 10 and 11 as separated waters at atmospheric conditions. [Spanish] Se desarrollo un procedimiento para estimar la incertidumbre analitica en cada parametro de analisis geoquimico de fluido geotermico. La estimacion de la incertidumbre esta basada en los resultados de los analisis geoquimicos de fluidos geotermicos (numerados del 0 al 14), obtenidos en el marco del programa de comparaciones entre los laboratorios geoquimicos en los ultimos 30 anos. Tambien se realizo la propagacion de la incertidumbre analitica en el calculo de los parametros del fluido geotermico en el yacimiento, a traves de los metodos de intervalo de incertidumbre y GUM (Guide to the expression of Uncertainty of Measurement). La aplicacion de los metodos se ilustra en el calculo de pH del fluido geotermico en el yacimiento, considerando las muestras 10 y 11 como aguas separadas a las condiciones atmosfericas.