Abstract: Geochemical analytical data are reported for 123 Cretaceous rock samples from northwestern Alberta collected by Alberta Geological Survey (AGS) staff from 2001 to 2005. The values for one repeat analysis are included (5602R), making a total of 124 analytical records. The results include analyses of 57 mudstone, 29 shale, 13 ironstone, 6 pyrite (float), 5 kimberlite (including one till clast) and 5 sandstone (including one bioclastic sandstone) samples. Geochemical analyses were performed by Acme Analytical Laboratories Ltd. of Vancouver, British Columbia, for a wide range of elements and oxides using the following analytical methods. (a) Method 1EX: four-acid (HF-HNO3-HClO4-HCl) digestion and inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS) multi-element analyses. (b) Method 1F: aqua regia digestion and inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS) multi-element analyses. (c) Method 2A: carbonate carbon (CO2), graphitic carbon, organic carbon and sulphate determined using a Leco carbon-sulphur analyzer. (d) Method 4A: fusion-HNO3 digestion and inductively coupled plasma atomic emission spectrometry (ICP-AES) analyses except for (i) total C and total S by Leco carbon-sulphur analyzer and (ii) loss on ignition (950 degrees C). (e) Method 4B: fusion-HNO3 digestion and inductively coupled plasma mass spectrometry (ICP-MS) analyses.
Metadata: 
  File identifier: 
      DIG_2006_0021.xml
  Language: 
      eng; CAN
  Character set: 
    Character set code: 
      utf8
  Hierarchy level: 
    Scope code: 
      dataset
  Metadata author: 
    Responsible party: 
      Organisation name: 
          Alberta Geological Survey
      Position name: 
          AGS Information Manager
      Contact info: 
        Contact: 
          Phone: 
            Telephone: 
              Voice: 
                  (780) 638-4491
              Facsimile: 
                  (780) 422-1918
          Address: 
            Address: 
              Delivery point: 
                  Alberta Energy Regulator
              Delivery point: 
                  4th Floor, Twin Atria Building
              Delivery point: 
                  4999-98 Avenue NW
              City: 
                  Edmonton
              Administrative area: 
                  Alberta
              Postal code: 
                  T6B 2X3
              Country: 
                  Canada
              Electronic mail address: 
                  AGS-Info@aer.ca
          Hours of service: 
              8:00 a.m. to 12:00 p.m. and 1:00 p.m. to 4:30 p.m.
      Role: 
        Role code: 
          pointOfContact
  Date stamp: 

      2016-03-29
  Metadata standard name: 
      North American Profile of ISO 19115:2003 - Geographic information - Metadata (NAP-Metadata)
  Metadata standard version: 
      ISO 19115-1.1
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Spatial representation info:

Vector spatial representation: Geometric objects: Geometric objects: Geometric object type: Geometric object type code: point Geometric object count: 124
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Reference system info:

Reference system:
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Reference system info:

xlink: https://www.ngdc.noaa.gov/docucomp/65f8b220-95ed-11e0-aa80-0800200c9a66 title: North American Datum 1983
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Reference system info:

xlink: https://www.ngdc.noaa.gov/docucomp/c3895520-95ed-11e0-aa80-0800200c9a66 title: Geodetic Reference System 1980
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Identification info:

Data identification: Citation: Citation: Title: Geochemical data for mudstones, shales and other Cretaceous rocks of northwestern Alberta Date: Date: Date: 2006-01-01 Date type: Date type code: publication Identifier: Identifier: Code: DIG 2006-021 Cited responsible party: Responsible party: Organisation name: Alberta Energy and Utilities Board Role: Role code: originator Cited responsible party: Responsible party: Organisation name: Alberta Geological Survey Role: Role code: originator Cited responsible party: Responsible party: Organisation name: Prior, G.J. Role: Role code: originator Cited responsible party: Responsible party: Organisation name: Pawlowicz, J.G. Role: Role code: originator Cited responsible party: Responsible party: Organisation name: Hathway, B. Role: Role code: originator Cited responsible party: Responsible party: Organisation name: Alberta Geological Survey Contact info: Contact: Address: Address: City: Edmonton Administrative area: Alberta, Canada Role: Role code: publisher Presentation form: Presentation form code: tableDigital Series: Series: Name: Digital Data Issue identification: DIG 2006-0021 Abstract: Geochemical analytical data are reported for 123 Cretaceous rock samples from northwestern Alberta collected by Alberta Geological Survey (AGS) staff from 2001 to 2005. The values for one repeat analysis are included (5602R), making a total of 124 analytical records. The results include analyses of 57 mudstone, 29 shale, 13 ironstone, 6 pyrite (float), 5 kimberlite (including one till clast) and 5 sandstone (including one bioclastic sandstone) samples. Geochemical analyses were performed by Acme Analytical Laboratories Ltd. of Vancouver, British Columbia, for a wide range of elements and oxides using the following analytical methods. (a) Method 1EX: four-acid (HF-HNO3-HClO4-HCl) digestion and inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS) multi-element analyses. (b) Method 1F: aqua regia digestion and inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS) multi-element analyses. (c) Method 2A: carbonate carbon (CO2), graphitic carbon, organic carbon and sulphate determined using a Leco carbon-sulphur analyzer. (d) Method 4A: fusion-HNO3 digestion and inductively coupled plasma atomic emission spectrometry (ICP-AES) analyses except for (i) total C and total S by Leco carbon-sulphur analyzer and (ii) loss on ignition (950 degrees C). (e) Method 4B: fusion-HNO3 digestion and inductively coupled plasma mass spectrometry (ICP-MS) analyses. Purpose: To release analytical data for 123 Cretaceous rock samples collected throughout northwestern Alberta by Alberta Geological Survey staff from 2001 to 2005. Status: Progress code: completed Point of contact: Responsible party: Organisation name: Alberta Geological Survey Position name: AGS Information Manager Contact info: Contact: Phone: Telephone: Voice: (780) 638-4491 Facsimile: (780) 422-1918 Address: Address: Delivery point: Alberta Energy Regulator Delivery point: 4th Floor, Twin Atria Building Delivery point: 4999-98 Avenue NW City: Edmonton Administrative area: Alberta Postal code: T6B 2X3 Country: Canada Electronic mail address: AGS-Info@aer.ca Hours of service: 8:00 a.m. to 12:00 p.m. and 1:00 p.m. to 4:30 p.m. Role: Role code: pointOfContact Resource maintenance: Maintenance information: Maintenance and update frequency: Maintenance frequency code: notPlanned Descriptive keywords: Keywords: Keyword: analysis Keyword: cretaceous Keyword: geochemical Keyword: geology Keyword: ironstone Keyword: kimberlite Keyword: mudstone Keyword: pyrite Keyword: rocks Keyword: sandstone Keyword: shale Keyword: siltstone Type: Keyword type code: theme Thesaurus name: Citation: Title: none Date: unknown Descriptive keywords: Keywords: Keyword: 83m Keyword: 83n Keyword: 83o Keyword: 84b Keyword: 84c Keyword: 84d Keyword: 84e Keyword: 84f Keyword: 84g Keyword: 84j Keyword: 84k Keyword: 84l Keyword: 84m Keyword: 84n Keyword: 84o Keyword: alberta Keyword: canada Type: Keyword type code: place Thesaurus name: Citation: Title: Date: unknown Resource constraints: Legal constraints: Access constraints: Restriction code: otherRestrictions Use constraints: Restriction code: otherRestrictions Other constraints: Access Constraints: Public Use Constraints: Acknowledgement of the Alberta Energy Regulator/Alberta Geological Survey as the originator/source of this information is required as described in the Open Government License - Alberta. Distribution Liability: The Alberta Energy Regulator/Alberta Geological Survey (AER/AGS) licenses this information under the Open Government License - Alberta. Any references to proprietary software in our documentation, and/or any use of proprietary data formats in our releases, do not constitute endorsement by the AER/AGS of any manufacturer's product. Spatial representation type: Spatial representation type code: vector Language: eng; CAN Topic category: Topic category code: geoscientificInformation Extent: Extent: Geographic element: Geographic bounding box: West bound longitude: -120 East bound longitude: -114 South bound latitude: 55 North bound latitude: 60 Temporal element: Temporal extent: Extent: Time period: Description: ground condition Begin date: 2001-01-01 End date: 2005-01-01 Supplemental Information: In English
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Content info:

Feature catalogue description: Included with dataset: false Feature catalogue citation: Citation: Title: Entity and Attribute Information Date: Other citation details: Detailed Entity and Attribute information is provided with the dataset, formatted as Federal Geographic Data Committee (FGDC) Content Standard for Digital Geospatial Metadata.
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DISTRIBUTION INFO:

Distribution: Distribution format: Format: Name: XLS (Microsoft Excel, 2003 11.6355.6360) Version: unknown File decompression technique: WinZip 8.0 (3105) Distributor: Distributor: Distributor contact: Responsible party: Organisation name: Alberta Geological Survey Position name: AGS Information Manager Contact info: Contact: Phone: Telephone: Voice: (780) 638-4491 Facsimile: (780) 422-1918 Address: Address: Delivery point: Alberta Energy Regulator Delivery point: 4th Floor, Twin Atria Building Delivery point: 4999-98 Avenue NW City: Edmonton Administrative area: Alberta Postal code: T6B 2X3 Country: Canada Electronic mail address: AGS-Info@aer.ca Hours of service: 8:00 a.m. to 12:00 p.m. and 1:00 p.m. to 4:30 p.m. Role: Role code: distributor Distribution Order Process: Standard order process: Fees: Free Transfer options: Digital transfer options: Online: Online Resource: Linkage: URL: https://static.ags.aer.ca/files/document/DIG/DIG_2006_0021.zip Name: Non-GIS Data
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Data quality info:

Data quality: Scope: Scope: Hierarchy level: Scope code: dataset Report: Absolute external positional accuracy: Name of measure: Horizontal Positional Accuracy Measure description: Evaluation method description: Field sample locations were obtained using hand-held GPS units without base station correction. The accuracy, as indicated by the GPS units when measurements were being obtained, is generally +/- 20 m or better. Result: Quantitative result: Value unit: Base unit: Identifier: Units system: xlink: http://www.bipm.org/en/si/ Value: Report: Completeness commission: Result: unknown Report: Completeness omission: Evaluation method description: Not all of the data returned by the analytical laboratory are included in this dataset. Analytical data for elements with poor quality control results were excluded, as were elements for which most or all of the analyses returned values of less than the lower detection limit. Result: unknown Report: Conceptual consistency: Measure description: The analytical data for approximately 17% of the samples were checked against the original laboratory reports to check for consistency and no errors were detected. One repeat analysis is present (5602R), so the total number of analytical records (124) exceeds the total number of samples by one. The repeat analysis was performed to more accurately determine the amount of phosphorus (P) and uranium (U) in sample 5602 by having the analytical laboratory insert high-P and high-U standards in the analytical batch. Included with the analytical results are average per cent recovery values, a measure of accuracy, based upon eight samples of CANMET certified reference material (standard) SY-4 (cf. Ziegler and Combs, 1997). Samples of SY-4 were weighted (12 to 25 g) and placed in vials by the AGS and included in batches of samples prior to shipment to the commercial analytical laboratory. The percentage recovery for each standard measurement is defined by the following equation: Percentage recovery = 100 x CM/CA where CM = the measured concentration of the standard sample CA = the actual concentration of the standard sample Percentage recovery values near 100% indicate a high degree of accuracy. Included with the analytical results are average relative per cent difference (RPD) values, a measure of precision, based upon up to ten duplicate sample pairs (cf. Ziegler and Combs, 1997; Zimmerman et al., 2001). The pairs include duplicates prepared before pulverization by AGS and duplicates prepared after pulverization by the analytical laboratory. The RPD for a set of duplicate pair results is defined by the following equation: RPD = 100 x [absolute value (C1 - C2)]/ CX where RPD = relative percentage difference C1 - C2 = the difference between the two concentrations CX = mean of the two results Low RPD values for the duplicate pairs indicate a high level of analytical precision. References Ziegler, A.C. and Combs, L.J. (1997): Baseline data-collection and quality-control protocols and procedures for the Equus beds ground-water recharge demonstration project near Wichita, Kansas, 1995-06; U.S. Geological Survey, Open-File Report 97-235, 23 p. Zimmerman, L.R., Strahan, A.P. and Thurman, E.M. (2001): Method of analysis and quality-assurance practices by the U.S. Geological Survey Organic Geochemistry Research Group - determination of four selected mosquito insecticides and a synergist in water using liquid-liquid extraction and gas chromatography/mass spectrometry; U.S. Geological Survey, Open-File Report 01-273, 11 p. Result: unknown Lineage: Lineage: Statement: Not all of the data returned by the analytical laboratory are included in this dataset. Analytical data for elements with poor quality control results were excluded, as were elements for which most or all of the analyses returned values of less than the lower detection limit. Process step: Process step: Description: The rock samples were collected from 2001 to 2005 (a) in the field by AGS staff, (b) from core stored at the Alberta Geological Survey (AGS) Mineral Core Research Facility (MCRF) in Edmonton, Alberta, and (c) from core stored at the Alberta Energy and Utilities Board (EUB) Core Research Centre in Calgary, Alberta. All analytical work, including sample preparation, was performed by Acme Analytical Laboratories Ltd. (Acme) of Vancouver, B.C. The method descriptions listed below were provided by Acme. Sample preparation: Samples were crushed and then pulverized using mild steel to <150 mesh (<0.100 mm). Four-Acid (HF-HNO3-HClO4-HCl) ICP-AES/MS Multi-Element Analyses (Acme Method 1EX): Acme completed four-acid digestion of the samples followed by inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS) analyses. Pulverized splits of 0.25 g were weighed into Teflon test tubes. A 10 mL aliquot of the acid solution (2:2:1:1 H2O-HF-HClO4-HNO3) was added, heated until fuming on a hot plate and taken to dryness. A 7.5 mL aliquot of 50% HCl was added to the residue and heated in a hot water bath (~95 degrees C) for 30 minutes. After cooling, the solutions were transferred to polypropylene test tubes and made to a 10 mL volume with 5% HCl. Solutions were analyzed by ICP-AES (Jarrel Ash AtomComp 800 ICP emission spectrometer) and ICP-MS (Perkin Elmer Elan 6000 ICP mass spectrometer). Elements with high concentrations, including major elements, are reported by ICP-AES, whereas elements with low concentrations (e.g., Be, Hf and Ta) are reported by ICP-MS. Elements that can span a broad range of concentrations (e.g., Cu, Pb and Zn) may be reported by either ICP-MS (low concentrations) or ICP-AES (high concentrations). Aqua Regia ICP-AES/MS Multi-Element Analyses (Acme Method 1F): Analyses were performed using 1 g to 15 g of material following Acme's 1F analytical procedure. The Acme version of aqua regia (equal proportions of HCl, HNO3 and demineralized H2O) was added to each sample in a ratio of 6 mL of aqua regia to 1 g of sample. Samples were digested for one hour in a hot water bath (90-95 degrees C) then diluted to a 20:1 mL/g final ratio. All sample solutions were analyzed by both ICP-AES (Jarrel Ash AtomComp 800 ICP emission spectrometer) and ICP-MS (Perkin Elmer Elan 6000 ICP mass spectrometer). ICP-AES values may be reported for several elements if concentrations exceeded laboratory-determined crossover values; otherwise, ICP-MS results are reported. Sulphate Sulphur (Acme Method 2A): Sample splits (0.1 g) in Leco crucibles were ignited at 800 degrees C for one hour to decompose sulphides and drive off the sulphur as SO2. Upon cooling the samples were analyzed in a Leco C244 Carbon-Sulphur analyzer. The sulphur determined is attributed to the presence of sulphur as sulphate. Carbonate Carbon as CO2 (Acme Method 2A): For each sample a pulp split of 0.2 g was weighed into 500 ml polypropylene bottle. A 34 mL aliquot of water was added. A test tube containing 6 mL of concentrated ACS grade HCLO4 was delicately placed inside the bottle. A cap fitted with two stopcocks was tightly screwed on. The bottle was tilted to allow the acid, water and sample to mix. The bottle was placed in a hot water bath (70 degrees C) for 30 minutes to help evolve CO2 into the gas phase. For sample analysis, the bottle was attached to a Leco C244 Carbon-Sulphur analyzer via the stopcocks. The CO2 was swept into the analyzer with an O2 carrier gas. The instrument determines and reports the carbon content from which the CO2 content is calculated. Graphitic Carbon (Acme Method 2A): The graphite-carbon content was determined by first removing the organic and carbonate-carbon fractions. Sample splits (0.1 g) were placed in Leco crucibles. Organic carbon was removed by igniting the samples for one hour at 600 degrees C. After cooling, the residues were leached with 15% HCl for one hour to remove the carbonate fraction. The residues were then analyzed using a Leco C244 Carbon-Sulphur analyzer. Induction flux was added to the residue and the samples were ignited at >1650 degrees C in an induction furnace. A carrier gas was used to sweep up released carbon to be measured by adsorption in an infrared spectrometric cell. Results are attributed to the presence of carbon as graphite. Organic Carbon (Acme Method 2A): After determination of the other forms of carbon, the organic carbon content is calculated as organic carbon = total carbon - graphitic carbon - carbonate carbon. Fusion ICP-AES Multi-Element Analyses (Acme Method 4A): Acme completed fusion digestion of the samples followed by inductively coupled plasma atomic emission spectrometry (ICP-AES) analyses. For each sample a 0.2 g sample aliquot was weighted into a graphite crucible and mixed with 1.5 g of LiBO2 flux. The flux/sample charge was heated in a muffle furnace for 15 minutes at 1050 degrees C. The molten mixture was removed and immediately poured into 100 mL of 5% HNO3 (ACS-grade nitric acid in demineralized water). The solution was shaken for two hours and then an aliquot was poured into a polypropylene test tube. Sample solutions were aspirated into an ICP emission spectrometer (Jarrel Ash Atomcomp Model 975). Determinations were made for SiO2, Al2O3, Fe2O3 (total Fe), MgO, CaO, Na2O, K2O, P2O5, MnO, Cr2O3, Ba, Ni, Sc and LOI. To determine Loss on Ignition (LOI), a 1 g sample split was ignited for 90 minutes at 950 degrees C, cooled in a desiccator and then weighted with the difference expressed as per cent Loss on Ignition. Total C and total S were determined on a 0.1 g sample split using a Leco C244 Carbon-Sulphur analyzer. Fusion ICP-MS Multi-Element Analyses (Acme Method 4B): Acme completed fusion digestion of the samples followed by inductively coupled plasma mass spectrometry (ICP-MS) analyses. A 0.2 g sample aliquot was weighted into a graphite crucible and mixed with 1.5 g of LiBO2 flux. The flux/sample charge was heated in a muffle furnace for 15 minutes at 1050 degrees C. The molten mixture was removed and immediately poured into 100 mL of 5% HNO3 (ACS-grade nitric acid in demineralized water). The solution was shaken for two hours, and then an aliquot was poured into a polypropylene test tube. Sample solutions were aspirated into an ICP mass spectrometer (Perkin-Elmer Elan 6000). Date and time: 2006-03-01T00:00:00
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Metadata constraints:

Legal constraints: Access constraints: Restriction code: otherRestrictions Use constraints: Restriction code: otherRestrictions Other constraints: Metadata Access Constraints: none Metadata Use Constraints: none
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Metadata maintenance:

Maintenance information: Maintenance and update frequency: unknown Maintenance note: This metadata was automatically generated from the FGDC Content Standard for Digital Geospatial Metadatastandard version FGDC-STD-001-1998 using the January 2013 version of the FGDC CSDGM to ISO 19115-2 transform. Metadata author: Responsible party: Organisation name: Alberta Geological Survey Position name: AGS Information Manager Contact info: Contact: Phone: Telephone: Voice: (780) 638-4491 Facsimile: (780) 422-1918 Address: Address: Delivery point: Alberta Energy Regulator Delivery point: 4th Floor, Twin Atria Building Delivery point: 4999-98 Avenue NW City: Edmonton Administrative area: Alberta Postal code: T6B 2X3 Country: Canada Electronic mail address: AGS-Info@aer.ca Hours of service: 8:00 a.m. to 12:00 p.m. and 1:00 p.m. to 4:30 p.m. Role: Role code: custodian
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