The theme on physicochemical monitoring of rivers and rivers presents data from all stations in networks monitoring water quality in rivers in Quebec and the St. Lawrence River.The purpose of networks for monitoring general water quality is to characterize, using current physicochemical and bacteriological parameters, the quality of water in spatial terms and to monitor the evolution of this quality over time. For the regular monitoring of the general quality of river and river water, the parameters measured are: total phosphorus, total nitrogen, nitrites and nitrates, ammonia nitrogen, chlorophyll a, pheopigments, faecal coliforms, faecal coliforms, turbidity, suspended matter, pH, conductivity, dissolved organic carbon and temperature. This data is used to calculate the Bacteriological and Physicochemical Water Quality Index (IQBP), a water quality classification index.The data set on physicochemical monitoring of rivers and rivers also includes the drainage areas of some of the stations. The attribute table provides a compilation of land use by category for the last year available at the time the data was generated. Follow-up is carried out annually.**This third party metadata element was translated using an automated translation tool (Amazon Translate).**

Description:Seasonal mean nitrate concentration from the British Columbia continental margin model (BCCM) were averaged over the 1981 to 2010 period to create seasonal mean climatology of the Canadian Pacific Exclusive Economic Zone.Methods:Nitrate concentrations at up to forty-six linearly interpolated vertical levels from surface to 2400 m and at the sea bottom are included. Spring months were defined as April to June, summer months were defined as July to September, fall months were defined as October to December, and winter months were defined as January to March. The data available here contain raster layers of seasonal nitrate concentration climatology for the Canadian Pacific Exclusive Economic Zone at 3 km spatial resolution and 47 vertical levels.Uncertainties:Model results have been extensively evaluated against observations (e.g. altimetry, CTD and nutrient profiles, observed geostrophic currents), which showed the model can reproduce with reasonable accuracy the main oceanographic features of the region including salient features of the seasonal cycle and the vertical and cross-shore gradient of water properties. However, the model resolution is too coarse to allow for an adequate representation of inlets, nearshore areas, and the Strait of Georgia.

Description:Seasonal mean nitrate concentration from the British Columbia continental margin model (BCCM) were averaged over the 1993 to 2020 period to create seasonal mean climatology of the Canadian Pacific Exclusive Economic Zone.Methods:Nitrate concentrations at up to forty-six linearly interpolated vertical levels from surface to 2400 m and at the sea bottom are included. Spring months were defined as April to June, summer months were defined as July to September, fall months were defined as October to December, and winter months were defined as January to March. The data available here contain raster layers of seasonal nitrate concentration climatology for the Canadian Pacific Exclusive Economic Zone at 3 km spatial resolution and 47 vertical levels.Uncertainties:Model results have been extensively evaluated against observations (e.g. altimetry, CTD and nutrient profiles, observed geostrophic currents), which showed the model can reproduce with reasonable accuracy the main oceanographic features of the region including salient features of the seasonal cycle and the vertical and cross-shore gradient of water properties. However, the model resolution is too coarse to allow for an adequate representation of inlets, nearshore areas, and the Strait of Georgia.

Patterns of wet deposition of the nitrate (NO3), non-sea-salt sulfate (xSO4) and ammonium (NH4) ions across areas of Canada and the United States are based on measurements of precipitation depth and ion concentrations in precipitation samples. xSO4 refers to the wet deposition of sulfate with the sea-salt sulfate contribution removed at coastal sites. These measurements were collected and quality controlled by their respective networks: in Canada, the federal Canadian Air and Precipitation Monitoring Network (CAPMoN) and provincial or territorial networks in Alberta, New Brunswick, the Northwest Territories, Nova Scotia, Ontario and Quebec. In the United States, wet deposition measurements were made by two coordinated networks: the National Atmospheric Deposition Program (NADP) / National Trends Network (NTN) and the NADP/Atmospheric Integrated Research Monitoring Network (AIRMoN). Only data from sites that were designated as regionally representative were used in the mapping. Wet deposition amounts were interpolated by ordinary kriging using ArcMap Geostatistical Analyst. The map is limited to the contiguous U.S. and southeastern or southern Canada because outside that region, the interpolation error exceeds 30% due to the larger distances between stations. Links to annual and five-year average maps are available in the associated resources.

Time series of dissolved inorganic nutrients (nitrate, silicate, phosphate) (mmol/m2) at the 3 fixed stations and 46 stations, grouped into transects, of the Atlantic Zonal Monitoring Program (AZMP) under the Quebec region responsibility.The mean integrated nutrient data of 2 strata (0-50 m) et (50-150 m) from the last ten years are displayed as 12 layers, 6 for the June survey (2013-2022, 2020 not sampled) and 6 for the autumn survey (2013-2022). Finally, 2 other layers shows the positions of the fixed stations of the program (Anticosti Gyre, Gaspé Current and Rimouski).Each station is linked with a .png file showing the time series of nutrients and with a .csv file containing all the integrated nutrient data acquired at those stations since the beginning of the program sampling (columns : Station, Latitude, Longitude, Date(UTC), Sounding(m), Depth_min/Profondeur_min(m), Depth_max/Profondeur_max(m), Integrated_Nitrate/Nitrate_intégré(mmol/m²), Integrated_Phosphate/Phosphate_intégré(mmol/m²), Integrated_Silicate/Silice_intégrée(mmol/m²)).PurposeThe Atlantic Zone Monitoring Program (AZMP) was implemented in 1998 with the aim of increasing the Department of Fisheries and Oceans Canada’s (DFO) capacity to detect, track and predict changes in the state and productivity of the marine environment.The AZMP collects data from a network of stations composed of high-frequency monitoring sites and cross-shelf sections in each following DFO region: Québec, Gulf, Maritimes and Newfoundland. The sampling design provides basic information on the natural variability in physical, chemical, and biological properties of the Northwest Atlantic continental shelf. Cross-shelf sections sampling provides detailed geographic information but is limited in a seasonal coverage while critically placed high-frequency monitoring sites complement the geography-based sampling by providing more detailed information on temporal changes in ecosystem properties.In Quebec region, two surveys (46 stations grouped into transects) are conducted every year, one in June and the other in autumn in the Estuary and Gulf of St. Lawrence. Historically, 3 fixed stations were sampled more frequently. One of these is the Rimouski station that still takes part of the program and is sampled about weekly throughout the summer and occasionally in the winter period.Annual reports (physical, biological and a Zonal Scientific Advice) are available from the Canadian Science Advisory Secretariat (CSAS), (http://www.dfo-mpo.gc.ca/csas-sccs/index-eng.htm).Devine, L., Scarratt, M., Plourde, S., Galbraith, P.S., Michaud, S., and Lehoux, C. 2017. Chemical and Biological Oceanographic Conditions in the Estuary and Gulf of St. Lawrence during 2015. DFO Can. Sci. Advis. Sec. Res. Doc. 2017/034. v + 48 pp.Supplemental InformationWater sampling for nutrients analysis is done from Niskin bottles according to AZMP sampling protocol:Mitchell, M. R., Harrison, G., Pauley, K., Gagné, A., Maillet, G., and Strain, P. 2002. Atlantic Zonal Monitoring Program sampling protocol. Can. Tech. Rep. Hydrogr. Ocean Sci. 223: iv + 23 pp.

Regional stream sediment geochemical data compilationNovember 2020Release notesThe 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:1. RGS_SITE_WATER - site specific physiography and water quality data. These data are unchanged from the original releases. 2. RGS_HEON - the same data as released in Héon (2003) with minor updates to sample location. 3. RGS_AAS - all samples analyzed by atomic absorption spectrometry. Most of these data are superseded by INAA and ICPMS data. 4. RGS_INAA - all samples analyzed by instrumental neutron activation analysis (INAA) and fire assay-neutron activation (FA-NA) analysis. 5. RGS_ICPMS - all samples analyzed by inductively coupled plasma mass spectrometry (ICPMS). 6. 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](mailto:YGSMinerals@yukon.ca) ; [geology@yukon.ca](mailto:geology@yukon.ca)Distributed from [GeoYukon](https://yukon.ca/geoyukon) by the [Government of Yukon](https://yukon.ca/maps) . Discover more digital map data and interactive maps from Yukon's digital map data collection.For more information: [geomatics.help@yukon.ca](mailto:geomatics.help@yukon.ca)

Regional stream sediment geochemical data compilationNovember 2020Release notesThe 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:1. RGS_SITE_WATER - site specific physiography and water quality data. These data are unchanged from the original releases. 2. RGS_HEON - the same data as released in Héon (2003) with minor updates to sample location. 3. RGS_AAS - all samples analyzed by atomic absorption spectrometry. Most of these data are superseded by INAA and ICPMS data. 4. RGS_INAA - all samples analyzed by instrumental neutron activation analysis (INAA) and fire assay-neutron activation (FA-NA) analysis. 5. RGS_ICPMS - all samples analyzed by inductively coupled plasma mass spectrometry (ICPMS). 6. 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](mailto:YGSMinerals@yukon.ca) ; [geology@yukon.ca](mailto:geology@yukon.ca)Distributed from [GeoYukon](https://yukon.ca/geoyukon) by the [Government of Yukon](https://yukon.ca/maps) . Discover more digital map data and interactive maps from Yukon's digital map data collection.For more information: [geomatics.help@yukon.ca](mailto:geomatics.help@yukon.ca)

Regional stream sediment geochemical data compilationNovember 2020Release notesThe 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:1. RGS_SITE_WATER - site specific physiography and water quality data. These data are unchanged from the original releases. 2. RGS_HEON - the same data as released in Héon (2003) with minor updates to sample location. 3. RGS_AAS - all samples analyzed by atomic absorption spectrometry. Most of these data are superseded by INAA and ICPMS data. 4. RGS_INAA - all samples analyzed by instrumental neutron activation analysis (INAA) and fire assay-neutron activation (FA-NA) analysis. 5. RGS_ICPMS - all samples analyzed by inductively coupled plasma mass spectrometry (ICPMS). 6. 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](mailto:YGSMinerals@yukon.ca) ; [geology@yukon.ca](mailto:geology@yukon.ca)Distributed from [GeoYukon](https://yukon.ca/geoyukon) by the [Government of Yukon](https://yukon.ca/maps) . Discover more digital map data and interactive maps from Yukon's digital map data collection.For more information: [geomatics.help@yukon.ca](mailto:geomatics.help@yukon.ca)

This dataset displays aquifers with water allocation notations on them. This dataset is updated daily.

This dataset includes water chemistry data collected from five of the six lakes as part of the Northwestern Ontario Size Series project in 1987 and 1990 including species of nitrogen and phosphorus, carbon, chlorophyll a, conductivity, soluble reactive silica, chloride, sulphate, conductivity, sodium, potassium, magnesium, calcium, pH, alkalinity and organic acids