A chlorophyll fluorescence time series was collected at various locations around the coast of Vancouver Island, British Columbia, Canada for monitoring phytoplankton concentrations. A Wetlabs ECO fluorometer was deployed every few months on a schedule depending on season and sensor availability. The instrument hung by a chain attached to the side of the buoy, or dock, depending on location, and measured chlorophyll using the fluorescence emission at 695nm. The instrument also measured turbidity by detecting the scattered light at 700nm. The units had internal batteries and data storage and were programmed to make a group of 5 measurements every 30 minutes. A copper wiper covered the sampling window between groups of measurements to reduce fouling. Times are in UTC unless otherwise stated.

This study aimed to identify chemical components that could distinguish chemical mixtures in oil sands process-affected water (OSPW) from natural groundwater sources. Oil sands process-affected samples were collected from two different oil sands development tailing ponds, and natural groundwater samples were collected from both far-field (greater than one kilometer (>1km) down- or upstream from an oil sands development site), and near-field (less than 200 meters (<200m) from an oil sands development site) locations.Water samples were assessed by geochemistry, total naphthenic acid analysis, and synchronous fluorescence spectroscopy (SFS) identifying those samples with acid-extractable organics (AEO). Using electrospray ionization high resolution mass spectrometry as well as multidimensional gas chromatography time-of-flight mass spectrometry profiling allowed for differentiation of natural from OSPW sources through the measurement of O2 : O4 ion class ratios. AEO profiles from OSPW and groundwater samples adjacent to tailings ponds were similar, suggesting a common source.All data are a part subject of a publication containing method details, full QA/QC, interpretation, and conclusions: Frank, R. A., Roy, J. W., Bickerton, G., Rowland, S. J., Headley, J. V., Scarlett, A. G., West, C. E., Peru, K. M., Parrott, J. L., Conly, F. M., & Hewitt, L. M. (2014). Profiling oil sands mixtures from industrial developments and natural groundwaters for source identification. Environmental science & technology, 48(5), 2660–2670. doi.org/10.1021/es500131kResponse to comment: Frank, R. A., Roy, J. W., Bickerton, G., Rowland, S. J., Headley, J. V., Scarlett, A. G., West, C. E., Peru, K. M., Parrott, J. L., Conly, F. M., & Hewitt, L. M. (2014). Response to Comment on "Profiling oil sands mixtures from industrial developments and natural groundwaters for source identification". Environmental science & technology, 48(18), 11015–11016. doi.org/10.1021/es504008z

Moored instrument time series data include current velocity, temperature, salinity, oxygen, fluorescence, transmissivity, turbidity, sediment trap data and particle capture of carbon, nitrogen, and silicon.These data were collected by researchers from the Institute of Ocean Sciences, Sidney, BC, from locations in the North Pacific.The data links below are only a representative sample of the entire collection. If you require more data, please send your request to the data contact.

Moored instrument time series data include current velocity, temperature, salinity, oxygen, fluorescence, transmissivity, turbidity, and particle capture of carbon, nitrogen, and silicon as well as sediment trap, ice drift and ice draft data.These data were collected by researchers from the Institute of Ocean Sciences, Sidney, BC, from locations ranging from the North Pacific, the Beaufort Sea, and across the Canadian Arctic Archipelago to Baffin Bay.

Moored instrument time series data include current velocity, temperature, salinity, oxygen, fluorescence, transmissivity, turbidity, and particle capture of carbon, nitrogen, and silicon. Also included are sediment trap, ice drift and ice draft data.These data were collected by researchers from the Institute of Ocean Sciences, Sidney, BC, from locations ranging from the Beaufort Sea, and across the Canadian Arctic Archipelago to Baffin Bay.The data links below are only a representative sample of the entire collection. If you require more data, please send your request to the data contact.

This dataset represents lithogeochemistry of Saskatchewan samples.This dataset represents lithogeochemistry of Saskatchewan samples. This dataset represents the exhaustive mapping and sampling program of the Athabasca Group between 1975 and 1981 by the Saskatchewan Geological Survey (SGS), the results of which are contained in Ramaekers (1990). These samples are now stored at the Ministry of Energy and Resources, Subsurface Geological Laboratory in Regina, Saskatchewan. A selection of these samples was chosen to help characterize the background geochemical signature of the Athabasca Group and to identify anomalous regions. A total of 837 samples were chosen. All samples in this data set were processed at the Geoanalytical Laboratories at the Saskatchewan Research Council (SRC) in Saskatoon, Saskatchewan, an ISO/IEC 17025:2005 certified facility (i.e., meets the General Requirements for the Competence of Mineral Testing and Calibration Laboratories). Samples were crushed, split, agate ground, and then run with Sandstone Exploration Package ICPMS 1. The package produces three separate analysis types: inductively coupled plasma mass spectroscopy (ICP MS) partial digestion for trace elements; ICP MS total digestion for trace elements; and ICP–Optical Emission Spectrometry (ICP–OES) total digestion for major and minor elements. Details and detection limits are available on the SRC’s website. ICP total digestion: a 0.250 g pulp is gently heated in a mixture of ultrapure HF/HNO3/HClO4until dry and the residue dissolved in dilute ultrapure HNO3; ICP MS total digestion: a 0.250 g pulp is gently heated in a mixture of ultrapure HF/HNO3/HClO4until dry and the residue dissolved in dilute ultrapure HNO3; ICP MS partial digestion: a 2.00 g pulp is digested with 2.25 ml of 8:1 ultrapure HNO3:HCl for 1 hour at 95° C; Detection limits are from the SRC's 2011 Analytical Fee Schedule; null values indicate that elements are below the detection limit. NOTE: Attribute data headings ending with TD indicate Total Digestion, those ending with PD indicate Partial Digestion. Majors oxides are in percent; all other elements are in ppm. **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. 

The Sentinel mirror is maintained by the Government of Canada through the Copernicus collaborative ground segment program as well as EUMETSAT. Data is made available as quickly as possible based on Canada coverage availability at the source. **This third party metadata element follows the Spatio Temporal Asset Catalog (STAC) specification.**

The Sentinel mirror is maintained by the Government of Canada through the Copernicus collaborative ground segment program as well as EUMETSAT. Data is made available as quickly as possible based on Canada coverage availability at the source. **This third party metadata element follows the Spatio Temporal Asset Catalog (STAC) specification.**

The Sentinel mirror is maintained by the Government of Canada through the Copernicus collaborative ground segment program as well as EUMETSAT. Data is made available as quickly as possible based on Canada coverage availability at the source. **This third party metadata element follows the Spatio Temporal Asset Catalog (STAC) specification.**

The Sentinel mirror is maintained by the Government of Canada through the Copernicus collaborative ground segment program as well as EUMETSAT. Data is made available as quickly as possible based on Canada coverage availability at the source. **This third party metadata element follows the Spatio Temporal Asset Catalog (STAC) specification.**