The index map of regional geochemical surveys covering the whole of Canada is available in this OGC WMS service. The map is presented as a single layer. For more information please visit http://geochem.nrcan.gc.ca

Regional stream sediment geochemical data compilation November 2020 Release notes The regional stream sediment geochemical data compilation comprises data for more than 30 000 samples across Yukon. This compilation updates the work of Héon (2003). This new compilation includes results from the reanalysis of more than 24 000 samples; inductively coupled plasma mass spectrometry (ICPMS) analysis provides upgraded detection limits and a broader range of elements relative to previous analytical data. In addition to analytical data, efforts have been made to improve sample location accuracy. The data in this release are organized by analytical method with the geodatabase having six feature classes: RGS_SITE_WATER - site specific physiography and water quality data. These data are unchanged from the original releases. RGS_HEON - the same data as released in Héon (2003) with minor updates to sample location. RGS_AAS - all samples analyzed by atomic absorption spectrometry. Most of these data are superseded by INAA and ICPMS data. RGS_INAA - all samples analyzed by instrumental neutron activation analysis (INAA) and fire assay-neutron activation (FA-NA) analysis. RGS_ICPMS - all samples analyzed by inductively coupled plasma mass spectrometry (ICPMS). RGS_All - includes all AAS, INAA and ICPMS data. Collection of stream sediment samples in Yukon began in 1976 and ended in 2006. Three analytical methods have been used to analyze the minus 0.177 mm fraction (-80 mesh) of these samples: AAS, INNA (and FA-NA) and ICPMS. A simple description of each method is given below. For atomic absorption spectrometry (AAS) a 1 g aliquot is 'partially digested' using Lefort aqua regia or concentrated hot nitric acid. The digestion product is analyzed using an atomic absorption spectrometer. Oxide and silicate minerals are partially digested while some sulphide minerals are erratically volatilized. This means that AAS cannot be used to obtain accurate REE, Ta, Nb, As, Sb, Sn, Hg, Cr, or Au determinations. For instrumental neutron activation analysis ( INAA), aliquots of sieved sediment (the minus 0.177 mm fraction) or milled rock ranging from 5 to 40 g are encapsulated and irradiated in a nuclear reactor before counting the primary gamma radiation induced by the neutron irradiation with a high resolution germanium gamma ray detector. Fire assay-neutron activation (FA-NA) analysis is similar but includes a pre-concentration fire assay step prior to irradiation and analysis. Results for both INAA and FA-NA are similar to those for samples analyses by fusion or other total digestion techniques. Neutron activation detection limits are typically higher than those by acid digestion - ICPMS. Commodity and pathfinder elements such as Au, As, Sb and W have reasonable detection limits by INAA and the data generated are relatively precise. For ICPMS analysis, aliquots of sieved sediment ( the minus 0.177 mm fraction) ranging from 0.5 to 1 g are prepared using a partial digestion technique, typically aqua regia, followed by analysis of dissolution product by ICPMS. Sulphide minerals are completely oxidized and dissolved whereas most oxide and silicate minerals are only partially digested. This means that results produced by partial digestion methods are acceptable for elements such as Ag, As, Mo, Ni, Pb, Sb, Tl, and Zn but values for elements such as Al, Ba, Cr, Fe, P, Sn, Ti, Y, and Zr are likely to not reflect the actual element concentration in a sample. The sample size used for routine RGS sample analysis is too small be representative of Au in the original sample and thus Au by aqua regia digestion - ICPMS has poor precision. Further upgrades to this database are not anticipated. All samples that could be found in the GSC-Ottawa warehouse have been reanalyzed using ICPMS. Any errors or omissions in this database should be reported to the Yukon Geological Survey. Your feedback contributes to improving the accuracy of the geoscience databases for Yukon. Contact: YGSMinerals@yukon.ca ; geology@yukon.ca Distributed from GeoYukon by the Government of Yukon . Discover more digital map data and interactive maps from Yukon's digital map data collection. For more information: geomatics.help@yukon.ca

Regional stream sediment geochemical data compilation November 2020 Release notes The regional stream sediment geochemical data compilation comprises data for more than 30 000 samples across Yukon. This compilation updates the work of Héon (2003). This new compilation includes results from the reanalysis of more than 24 000 samples; inductively coupled plasma mass spectrometry (ICPMS) analysis provides upgraded detection limits and a broader range of elements relative to previous analytical data. In addition to analytical data, efforts have been made to improve sample location accuracy. The data in this release are organized by analytical method with the geodatabase having six feature classes: RGS_SITE_WATER - site specific physiography and water quality data. These data are unchanged from the original releases. RGS_HEON - the same data as released in Héon (2003) with minor updates to sample location. RGS_AAS - all samples analyzed by atomic absorption spectrometry. Most of these data are superseded by INAA and ICPMS data. RGS_INAA - all samples analyzed by instrumental neutron activation analysis (INAA) and fire assay-neutron activation (FA-NA) analysis. RGS_ICPMS - all samples analyzed by inductively coupled plasma mass spectrometry (ICPMS). RGS_All - includes all AAS, INAA and ICPMS data. Collection of stream sediment samples in Yukon began in 1976 and ended in 2006. Three analytical methods have been used to analyze the minus 0.177 mm fraction (-80 mesh) of these samples: AAS, INNA (and FA-NA) and ICPMS. A simple description of each method is given below. For atomic absorption spectrometry (AAS) a 1 g aliquot is 'partially digested' using Lefort aqua regia or concentrated hot nitric acid. The digestion product is analyzed using an atomic absorption spectrometer. Oxide and silicate minerals are partially digested while some sulphide minerals are erratically volatilized. This means that AAS cannot be used to obtain accurate REE, Ta, Nb, As, Sb, Sn, Hg, Cr, or Au determinations. For instrumental neutron activation analysis ( INAA), aliquots of sieved sediment (the minus 0.177 mm fraction) or milled rock ranging from 5 to 40 g are encapsulated and irradiated in a nuclear reactor before counting the primary gamma radiation induced by the neutron irradiation with a high resolution germanium gamma ray detector. Fire assay-neutron activation (FA-NA) analysis is similar but includes a pre-concentration fire assay step prior to irradiation and analysis. Results for both INAA and FA-NA are similar to those for samples analyses by fusion or other total digestion techniques. Neutron activation detection limits are typically higher than those by acid digestion - ICPMS. Commodity and pathfinder elements such as Au, As, Sb and W have reasonable detection limits by INAA and the data generated are relatively precise. For ICPMS analysis, aliquots of sieved sediment ( the minus 0.177 mm fraction) ranging from 0.5 to 1 g are prepared using a partial digestion technique, typically aqua regia, followed by analysis of dissolution product by ICPMS. Sulphide minerals are completely oxidized and dissolved whereas most oxide and silicate minerals are only partially digested. This means that results produced by partial digestion methods are acceptable for elements such as Ag, As, Mo, Ni, Pb, Sb, Tl, and Zn but values for elements such as Al, Ba, Cr, Fe, P, Sn, Ti, Y, and Zr are likely to not reflect the actual element concentration in a sample. The sample size used for routine RGS sample analysis is too small be representative of Au in the original sample and thus Au by aqua regia digestion - ICPMS has poor precision. Further upgrades to this database are not anticipated. All samples that could be found in the GSC-Ottawa warehouse have been reanalyzed using ICPMS. Any errors or omissions in this database should be reported to the Yukon Geological Survey. Your feedback contributes to improving the accuracy of the geoscience databases for Yukon. Contact: YGSMinerals@yukon.ca ; geology@yukon.ca Distributed from GeoYukon by the Government of Yukon . Discover more digital map data and interactive maps from Yukon's digital map data collection. For more information: geomatics.help@yukon.ca

Regional stream sediment geochemical data compilation November 2020 Release notes The regional stream sediment geochemical data compilation comprises data for more than 30 000 samples across Yukon. This compilation updates the work of Héon (2003). This new compilation includes results from the reanalysis of more than 24 000 samples; inductively coupled plasma mass spectrometry (ICPMS) analysis provides upgraded detection limits and a broader range of elements relative to previous analytical data. In addition to analytical data, efforts have been made to improve sample location accuracy. The data in this release are organized by analytical method with the geodatabase having six feature classes: RGS_SITE_WATER - site specific physiography and water quality data. These data are unchanged from the original releases. RGS_HEON - the same data as released in Héon (2003) with minor updates to sample location. RGS_AAS - all samples analyzed by atomic absorption spectrometry. Most of these data are superseded by INAA and ICPMS data. RGS_INAA - all samples analyzed by instrumental neutron activation analysis (INAA) and fire assay-neutron activation (FA-NA) analysis. RGS_ICPMS - all samples analyzed by inductively coupled plasma mass spectrometry (ICPMS). RGS_All - includes all AAS, INAA and ICPMS data. Collection of stream sediment samples in Yukon began in 1976 and ended in 2006. Three analytical methods have been used to analyze the minus 0.177 mm fraction (-80 mesh) of these samples: AAS, INNA (and FA-NA) and ICPMS. A simple description of each method is given below. For atomic absorption spectrometry (AAS) a 1 g aliquot is 'partially digested' using Lefort aqua regia or concentrated hot nitric acid. The digestion product is analyzed using an atomic absorption spectrometer. Oxide and silicate minerals are partially digested while some sulphide minerals are erratically volatilized. This means that AAS cannot be used to obtain accurate REE, Ta, Nb, As, Sb, Sn, Hg, Cr, or Au determinations. For instrumental neutron activation analysis ( INAA), aliquots of sieved sediment (the minus 0.177 mm fraction) or milled rock ranging from 5 to 40 g are encapsulated and irradiated in a nuclear reactor before counting the primary gamma radiation induced by the neutron irradiation with a high resolution germanium gamma ray detector. Fire assay-neutron activation (FA-NA) analysis is similar but includes a pre-concentration fire assay step prior to irradiation and analysis. Results for both INAA and FA-NA are similar to those for samples analyses by fusion or other total digestion techniques. Neutron activation detection limits are typically higher than those by acid digestion - ICPMS. Commodity and pathfinder elements such as Au, As, Sb and W have reasonable detection limits by INAA and the data generated are relatively precise. For ICPMS analysis, aliquots of sieved sediment ( the minus 0.177 mm fraction) ranging from 0.5 to 1 g are prepared using a partial digestion technique, typically aqua regia, followed by analysis of dissolution product by ICPMS. Sulphide minerals are completely oxidized and dissolved whereas most oxide and silicate minerals are only partially digested. This means that results produced by partial digestion methods are acceptable for elements such as Ag, As, Mo, Ni, Pb, Sb, Tl, and Zn but values for elements such as Al, Ba, Cr, Fe, P, Sn, Ti, Y, and Zr are likely to not reflect the actual element concentration in a sample. The sample size used for routine RGS sample analysis is too small be representative of Au in the original sample and thus Au by aqua regia digestion - ICPMS has poor precision. Further upgrades to this database are not anticipated. All samples that could be found in the GSC-Ottawa warehouse have been reanalyzed using ICPMS. Any errors or omissions in this database should be reported to the Yukon Geological Survey. Your feedback contributes to improving the accuracy of the geoscience databases for Yukon. Contact: YGSMinerals@yukon.ca ; geology@yukon.ca Distributed from GeoYukon by the Government of Yukon . Discover more digital map data and interactive maps from Yukon's digital map data collection. For more information: geomatics.help@yukon.ca

Regional stream sediment geochemical data compilation November 2020 Release notes The regional stream sediment geochemical data compilation comprises data for more than 30 000 samples across Yukon. This compilation updates the work of Héon (2003). This new compilation includes results from the reanalysis of more than 24 000 samples; inductively coupled plasma mass spectrometry (ICPMS) analysis provides upgraded detection limits and a broader range of elements relative to previous analytical data. In addition to analytical data, efforts have been made to improve sample location accuracy. The data in this release are organized by analytical method with the geodatabase having six feature classes: RGS_SITE_WATER - site specific physiography and water quality data. These data are unchanged from the original releases. RGS_HEON - the same data as released in Héon (2003) with minor updates to sample location. RGS_AAS - all samples analyzed by atomic absorption spectrometry. Most of these data are superseded by INAA and ICPMS data. RGS_INAA - all samples analyzed by instrumental neutron activation analysis (INAA) and fire assay-neutron activation (FA-NA) analysis. RGS_ICPMS - all samples analyzed by inductively coupled plasma mass spectrometry (ICPMS). RGS_All - includes all AAS, INAA and ICPMS data. Collection of stream sediment samples in Yukon began in 1976 and ended in 2006. Three analytical methods have been used to analyze the minus 0.177 mm fraction (-80 mesh) of these samples: AAS, INNA (and FA-NA) and ICPMS. A simple description of each method is given below. For atomic absorption spectrometry (AAS) a 1 g aliquot is 'partially digested' using Lefort aqua regia or concentrated hot nitric acid. The digestion product is analyzed using an atomic absorption spectrometer. Oxide and silicate minerals are partially digested while some sulphide minerals are erratically volatilized. This means that AAS cannot be used to obtain accurate REE, Ta, Nb, As, Sb, Sn, Hg, Cr, or Au determinations. For instrumental neutron activation analysis ( INAA), aliquots of sieved sediment (the minus 0.177 mm fraction) or milled rock ranging from 5 to 40 g are encapsulated and irradiated in a nuclear reactor before counting the primary gamma radiation induced by the neutron irradiation with a high resolution germanium gamma ray detector. Fire assay-neutron activation (FA-NA) analysis is similar but includes a pre-concentration fire assay step prior to irradiation and analysis. Results for both INAA and FA-NA are similar to those for samples analyses by fusion or other total digestion techniques. Neutron activation detection limits are typically higher than those by acid digestion - ICPMS. Commodity and pathfinder elements such as Au, As, Sb and W have reasonable detection limits by INAA and the data generated are relatively precise. For ICPMS analysis, aliquots of sieved sediment ( the minus 0.177 mm fraction) ranging from 0.5 to 1 g are prepared using a partial digestion technique, typically aqua regia, followed by analysis of dissolution product by ICPMS. Sulphide minerals are completely oxidized and dissolved whereas most oxide and silicate minerals are only partially digested. This means that results produced by partial digestion methods are acceptable for elements such as Ag, As, Mo, Ni, Pb, Sb, Tl, and Zn but values for elements such as Al, Ba, Cr, Fe, P, Sn, Ti, Y, and Zr are likely to not reflect the actual element concentration in a sample. The sample size used for routine RGS sample analysis is too small be representative of Au in the original sample and thus Au by aqua regia digestion - ICPMS has poor precision. Further upgrades to this database are not anticipated. All samples that could be found in the GSC-Ottawa warehouse have been reanalyzed using ICPMS. Any errors or omissions in this database should be reported to the Yukon Geological Survey. Your feedback contributes to improving the accuracy of the geoscience databases for Yukon. Contact: YGSMinerals@yukon.ca ; geology@yukon.ca Distributed from GeoYukon by the Government of Yukon . Discover more digital map data and interactive maps from Yukon's digital map data collection. For more information: geomatics.help@yukon.ca

Regional stream sediment geochemical data compilation November 2020 Release notes The regional stream sediment geochemical data compilation comprises data for more than 30 000 samples across Yukon. This compilation updates the work of Héon (2003). This new compilation includes results from the reanalysis of more than 24 000 samples; inductively coupled plasma mass spectrometry (ICPMS) analysis provides upgraded detection limits and a broader range of elements relative to previous analytical data. In addition to analytical data, efforts have been made to improve sample location accuracy. The data in this release are organized by analytical method with the geodatabase having six feature classes: RGS_SITE_WATER - site specific physiography and water quality data. These data are unchanged from the original releases. RGS_HEON - the same data as released in Héon (2003) with minor updates to sample location. RGS_AAS - all samples analyzed by atomic absorption spectrometry. Most of these data are superseded by INAA and ICPMS data. RGS_INAA - all samples analyzed by instrumental neutron activation analysis (INAA) and fire assay-neutron activation (FA-NA) analysis. RGS_ICPMS - all samples analyzed by inductively coupled plasma mass spectrometry (ICPMS). RGS_All - includes all AAS, INAA and ICPMS data. Collection of stream sediment samples in Yukon began in 1976 and ended in 2006. Three analytical methods have been used to analyze the minus 0.177 mm fraction (-80 mesh) of these samples: AAS, INNA (and FA-NA) and ICPMS. A simple description of each method is given below. For atomic absorption spectrometry (AAS) a 1 g aliquot is 'partially digested' using Lefort aqua regia or concentrated hot nitric acid. The digestion product is analyzed using an atomic absorption spectrometer. Oxide and silicate minerals are partially digested while some sulphide minerals are erratically volatilized. This means that AAS cannot be used to obtain accurate REE, Ta, Nb, As, Sb, Sn, Hg, Cr, or Au determinations. For instrumental neutron activation analysis ( INAA), aliquots of sieved sediment (the minus 0.177 mm fraction) or milled rock ranging from 5 to 40 g are encapsulated and irradiated in a nuclear reactor before counting the primary gamma radiation induced by the neutron irradiation with a high resolution germanium gamma ray detector. Fire assay-neutron activation (FA-NA) analysis is similar but includes a pre-concentration fire assay step prior to irradiation and analysis. Results for both INAA and FA-NA are similar to those for samples analyses by fusion or other total digestion techniques. Neutron activation detection limits are typically higher than those by acid digestion - ICPMS. Commodity and pathfinder elements such as Au, As, Sb and W have reasonable detection limits by INAA and the data generated are relatively precise. For ICPMS analysis, aliquots of sieved sediment ( the minus 0.177 mm fraction) ranging from 0.5 to 1 g are prepared using a partial digestion technique, typically aqua regia, followed by analysis of dissolution product by ICPMS. Sulphide minerals are completely oxidized and dissolved whereas most oxide and silicate minerals are only partially digested. This means that results produced by partial digestion methods are acceptable for elements such as Ag, As, Mo, Ni, Pb, Sb, Tl, and Zn but values for elements such as Al, Ba, Cr, Fe, P, Sn, Ti, Y, and Zr are likely to not reflect the actual element concentration in a sample. The sample size used for routine RGS sample analysis is too small be representative of Au in the original sample and thus Au by aqua regia digestion - ICPMS has poor precision. Further upgrades to this database are not anticipated. All samples that could be found in the GSC-Ottawa warehouse have been reanalyzed using ICPMS. Any errors or omissions in this database should be reported to the Yukon Geological Survey. Your feedback contributes to improving the accuracy of the geoscience databases for Yukon. Contact: YGSMinerals@yukon.ca ; geology@yukon.ca Distributed from GeoYukon by the Government of Yukon . Discover more digital map data and interactive maps from Yukon's digital map data collection. For more information: geomatics.help@yukon.ca

Regional stream sediment geochemical data compilation November 2020 Release notes The regional stream sediment geochemical data compilation comprises data for more than 30 000 samples across Yukon. This compilation updates the work of Héon (2003). This new compilation includes results from the reanalysis of more than 24 000 samples; inductively coupled plasma mass spectrometry (ICPMS) analysis provides upgraded detection limits and a broader range of elements relative to previous analytical data. In addition to analytical data, efforts have been made to improve sample location accuracy. The data in this release are organized by analytical method with the geodatabase having six feature classes: RGS_SITE_WATER - site specific physiography and water quality data. These data are unchanged from the original releases. RGS_HEON - the same data as released in Héon (2003) with minor updates to sample location. RGS_AAS - all samples analyzed by atomic absorption spectrometry. Most of these data are superseded by INAA and ICPMS data. RGS_INAA - all samples analyzed by instrumental neutron activation analysis (INAA) and fire assay-neutron activation (FA-NA) analysis. RGS_ICPMS - all samples analyzed by inductively coupled plasma mass spectrometry (ICPMS). RGS_All - includes all AAS, INAA and ICPMS data. Collection of stream sediment samples in Yukon began in 1976 and ended in 2006. Three analytical methods have been used to analyze the minus 0.177 mm fraction (-80 mesh) of these samples: AAS, INNA (and FA-NA) and ICPMS. A simple description of each method is given below. For atomic absorption spectrometry (AAS) a 1 g aliquot is 'partially digested' using Lefort aqua regia or concentrated hot nitric acid. The digestion product is analyzed using an atomic absorption spectrometer. Oxide and silicate minerals are partially digested while some sulphide minerals are erratically volatilized. This means that AAS cannot be used to obtain accurate REE, Ta, Nb, As, Sb, Sn, Hg, Cr, or Au determinations. For instrumental neutron activation analysis ( INAA), aliquots of sieved sediment (the minus 0.177 mm fraction) or milled rock ranging from 5 to 40 g are encapsulated and irradiated in a nuclear reactor before counting the primary gamma radiation induced by the neutron irradiation with a high resolution germanium gamma ray detector. Fire assay-neutron activation (FA-NA) analysis is similar but includes a pre-concentration fire assay step prior to irradiation and analysis. Results for both INAA and FA-NA are similar to those for samples analyses by fusion or other total digestion techniques. Neutron activation detection limits are typically higher than those by acid digestion - ICPMS. Commodity and pathfinder elements such as Au, As, Sb and W have reasonable detection limits by INAA and the data generated are relatively precise. For ICPMS analysis, aliquots of sieved sediment ( the minus 0.177 mm fraction) ranging from 0.5 to 1 g are prepared using a partial digestion technique, typically aqua regia, followed by analysis of dissolution product by ICPMS. Sulphide minerals are completely oxidized and dissolved whereas most oxide and silicate minerals are only partially digested. This means that results produced by partial digestion methods are acceptable for elements such as Ag, As, Mo, Ni, Pb, Sb, Tl, and Zn but values for elements such as Al, Ba, Cr, Fe, P, Sn, Ti, Y, and Zr are likely to not reflect the actual element concentration in a sample. The sample size used for routine RGS sample analysis is too small be representative of Au in the original sample and thus Au by aqua regia digestion - ICPMS has poor precision. Further upgrades to this database are not anticipated. All samples that could be found in the GSC-Ottawa warehouse have been reanalyzed using ICPMS. Any errors or omissions in this database should be reported to the Yukon Geological Survey. Your feedback contributes to improving the accuracy of the geoscience databases for Yukon. Contact: YGSMinerals@yukon.ca ; geology@yukon.ca Distributed from GeoYukon by the Government of Yukon . Discover more digital map data and interactive maps from Yukon's digital map data collection. For more information: geomatics.help@yukon.ca

A location line is defined as a straight line opened or indicated throughout between No. 1 and No. 2 location posts of a mineral claim and joining them. Distributed from GeoYukon by the Government of Yukon . Discover more digital map data and interactive maps from Yukon's digital map data collection. For more information: geomatics.help@yukon.ca

This dataset represents Lake Sediment Geochemical Analyses for the province of Saskatchewan. This dataset represents Lake Sediment Geochemical Analyses for the province of Saskatchewan. During the intense level of activity directed toward the exploration for uranium in the 1970s, the Saskatchewan Geological Survey and the Geological Survey of Canada funded the collection of several thousand samples of sediments and waters from lakes around the Athabasca Sandstone. All sediment samples were analyzed for U, Cu, Ni, Pb, Zn, Co, Fe and Mn. Selected samples were analyzed for a wide range of additional elements. All lake waters were analyzed for U, F-, and pH, and several hundred samples were analyzed for additional elements and parameters. The Summary Table that precedes this text shows the numbers of samples and elements, and the source of data from which the 8,939 samples listed in the 9 Tables are derived. Over 20 years ago the data in these listings were coded into the Saskatchewan Geological Survey’s ‘Geochemical Data File’, designed in the 1970s (Dunn, 1978b, 1979), and developed by SaskComp (the computer programming department of the Saskatchewan government at that time). The only database listed in the present report that was not in the Geochemical Data File was GSC Open File #779, jointly produced by the SGS and GSC (Coker and Dunn, 1981, 1983) and containing data from detailed surveys of the IAEA/NEA Athabasca Test Area (adjacent to Wollaston Lake). The old Geochemical Data File was state-of-the-art at the time, and data have been available for public scrutiny since inception in 1977. Demonstrations of the File were given at the SGS Open House meetings in 1977 and 1978. The explosive development of personal computers during the past 20 years has made the original Geochemical Data File something of a dinosaur, and the data have been difficult to access and manipulate. The present data file is a compilation that has resulted from detailed evaluation, streamlining, editing and breakdown of the data into simplified Excel files that can easily be manipulated by anyone with a modest knowledge of computers. These data are of historic value and their re-evaluation could assist in current uranium exploration programs. Of particular value is their use in environmental studies, since they represent a 1970s snapshot of the chemistry of the northern Saskatchewan environment prior to mine developments. At the start of sample collection in 1975 Key Lake had not been drained and the only mine site was the pit at Rabbit Lake. This compilation has divided the data into 9 tables, each presented as a shape file. There are 6 shape files of lake sediment data (1LS - 6LS) and 3 shape files of lake water data (4LW - 6LW). Lake water samples were from the same sites as the lake sediments listed in files 4LS - 6LS, hence they have been given the same numeric designation. The data are mostly compatible among the Tables. However, although analytical methods and quality control protocols were similar, they were sufficiently different to warrant treating the data as separate listings. For any regional plotting of data extracted from all Tables these differences should be considered when interpreting distribution patterns. Of particular relevance is that all sediment samples were analyzed for U by neutron activation, with the exception of 158 samples (Table 2LS) where determinations were by fluorometry. These data sets should be fully compatible, because the two techniques provide similar values. Comparison of U data from sediment samples collected and analyzed over four years, then reanalyzed as one batch has shown excellent precision and accuracy (Coker and Dunn, 1981). All U in water determinations were by fluorometry, and all F- by selective ion electrode. Loss on ignition (LOI) data were determined by ignition at 500o C for 4 hours. Table 1LS This data set comprises samples collected by SGS between 1975 and 1978. Samples were digested in aqua regia and all trace elements, except U (see above), were determined by atomic absorption spectrometry (AA).  **Please Note – All published Saskatchewan Geological Survey datasets, including those available through the Saskatchewan Mining and Petroleum GeoAtlas, are sourced from the Enterprise GIS Data Warehouse. They are therefore identical and share the same refresh schedule.

2020 DATABASE (Excel): The joint federal-provincial Regional Geochemical Surveys (RGS) have been carried out in British Columbia since 1976 as part of the National Geochemical Reconnaissance (NGR) program to aid exploration and development of mineral resources. The British Columbia Geological Survey (BCGS) maintains provincial geochemical databases capturing information from multi-media surveys. This 2020 release of the most current and complete province-wide geochemical data set collected under the (RGS) program. The database was compiled from 116 original sources with 65,429 samples and about 5 million determinations analyzed using 18 methods in 18 laboratories. This release augments the database with new RGS data compiled from BCGS and Geoscience BC publications between 2016 and 2019. Compared with the data in the last release, data in this release have been given further quality control treatment and revision. For the ease of use and consistency with previously published data, the data set was generated from the RGS database in a flat tabular format. The 2020 data set, released as BCGS GeoGile 2020-08, is presented in two MS Excel files, ‘RGS2020_ data.xlsx’ and ‘RGS2020_metadata.xlsx’. The data tables capture locations, field observations, analytical results and laboratories, and geology underlying sample sites for stream-, lake- and moss-sediment, water and lake samples, heavy mineral concentrates, tree twig, and needle ash. The analytical determinations include up to 63 analytes from sediment samples and up to 78 analytes from water samples. These samples, collected at an average density of about 1 site per 7–13 km2, provide representative geochemical data for the catchment basin upstream from the sample site. The RGS currently covers approximately 80 percent of the province.