Loading...
HomeMy WebLinkAboutDRC-2014-004582 - 0901a068804757c1ENERGY FUELS Energy Fuels Resources (USA) Inc. 225 Union Blvd. Suite 600 Lakewood, CO. US, 80228 303 974 2140 www.energyfuels.com Mr. Bryce Bird Director, Utah Division of Air Quality State of Utah Department of Environmental Quality VIA EMAIL AND OVERNIGHT DELIVERY July 29, 2014 195 North 1950 West Salt Lake City, UT 84116 DRC-2014-004582 Re: White Mesa Uranium Mill, National Emissions Standards for Radon Emission from Operating Mill Tailings Transmittal of June 2014 Monthly Radon Flux Monitoring Report for Cell 2 Dear Mr. Bird: This letter transmits Energy Fuels Resources (USA) Inc.'s ("EFRI's") radon-222 flux monitoring report for June 2014 (the "Monthly Report") consistent with 40 CFR 61.254(b), for Cell 2 at the White Mesa Uranium Mill (the "Mill"). Included with this Monthly Report is a Radon Flux Measurement Program Report, dated June 2014, prepared by Tellco Environmental (the "Tellco June 2014 Monthly Report"). The Tellco June 2014 Monthly Report indicates that for the month of June 2014, the average radon flux from Cell 2 was 15.0 pCi/(m2 -sec), which is lower than the 20 pCi/(m2 -sec) set out in 40 CFR 61.252(a). As discussed in the attached Monthly Report, the radon flux from Cell 2 during 2012 was higher than the 20 pCi/(m2 -sec) set out in 40 CFR 61.252(a). Although Cell 2 is no longer in operation, consistent with 40 CFR 61.254b, EFRI chose to perform monthly radon flux monitoring beginning the month immediately following submittal of the report for the year in non-compliance. The result of the 2013 radon-222 flux monitoring for Cell 2 was 20.4 pCi/(m" -sec) (averaged over 9 monthly sampling events), which slightly exceeds the 20 pCi/(m" -sec). Monthly sampling for Cell 2 has been conducted since April of 2013. A summary of the events that gave rise to EFRI's decision to monitor radon flux at Cell 2 monthly consistent with 40 CFR 61.254(b) is set out in Section 4.0 in the attached Monthly Report. EFRI has submitted monthly reports from May 2013 through July 2014 summarizing the April 2013 through June 2014 monthly sampling at Cell 2. A summary of the monthly Cell 2 radon flux measurements, as well as the date the EFRI monthly reports were submitted to the Utah Division of Air Quality ("UDAQ"), is included as Table 1 to this letter. EFRI began interim mitigation of radon flux from Cell 2 in 2013, as a result of the 2012 monitoring results, by applying one foot of additional soil cover to areas of Cell 2 with elevated radon. Details of the interim radon mitigation cover construction activities and interim corrective actions are described in Section 7.1 and 7.2 of the attached Monthly Report, respectively. EFRI completed the first phase of the interim cover installation on 12 test areas in September of 2013. The effectiveness of the additional N:\WMM\Required Reports\NESHAPS Reports\2014 Monthly NESHAPs reportsUune 2014\transmittal ltr June 2014.doc Letter to B. Bird July 29, 2014 Page 2 of 2 compacted cover at the 12 test areas was evaluated over several months. The additional cover on the 12 test areas was successful in achieving the desired reduction to 20 pCi/(m2-sec) or lower. As a result, EFRI applied additional random fill at 90% compaction to other areas of Cell 2 to further reduce the radon flux measurements. Based on the results in Table 1, EFRI submitted a Request to Cease Monthly Sampling on May 30, 2014 with the April 2014 Monthly Report. On July 23, 2014 EFRI received approval from UDAQ and the Utah Division of Radiation Control to cease monthly sampling, and therefore, this will be the last monthly report submitted. Future sampling will be conducted in accordance with the requirements described in the July 23, 2014 letter. If you have any questions, please feel free to contact me at (303) 389-4167. Yours very truly, Energy Fuels Resources (USA) Inc. Jaime Massey Regulatory Compliance Specialist cc: David C. Frydenlund Phil Goble, Utah DRC Dan Hillsten Rusty Lundberg, Utah DRC Jay Morris, Utah DAQ Harold R. Roberts Frank Filas David E. Turk Kathy Weinel Director, Air and Toxics Technical Enforcement Program, Office of Enforcement, Compliance and Environmental Justice, U. S. Environmental Protection Agency Attachments Table 1 Cell 2 Monthly Radon Flux Sampling Sampling Event Result (pCi/(m2 -sec)) Monthly Report Submittal Date 2012 Average 25.9 April 2013 18.0 May 29, 2013 May 2013 22.6 June 20, 2013 June 2013 23.2 July 25, 2013 July 2013 24.2 August 20, 2013 August 2013 30.2 September 23, 2013 September 2013 17.0 October 23,2013 October 2013 19.0 November 15, 2013 November 2013 19.5 December 17, 2013 December 2013 10.0 January 15, 2014 2013 Average 20.4 January 2014 9.8 February 27, 2014 February 2014 11.0 March 27, 2014 March 2014 16.4 April 25,2014 April 2014 13.3 May 30, 2014 May 2014 16.7 June 25, 2014 June 2014 15.0 July 29, 2014 2014 Average 13.7 Average since April 2013 17.1 ENERGY FUELS RESOURCES (USA) INC. 40 CODE OF FEDERAL REGULATIONS 61 SUBPART W WHITE MESA MILL SAN JUAN COUNTY, UTAH TAILINGS CELL 2 MONTHLY COMPLIANCE REPORT FOR JUNE 2014 Submitted July 29, 2014 by Energy Fuels Resources (USA) Inc. 225 Union Blvd. Suite 600 Lakewood, Colorado 80228 (303) 974-2140 Table of Contents 1.0 Name and Location of the Facility 3 2.0 Monthly Report 3 3.0 Name of the Person Responsible for Operation and Preparer of Report 3 4.0 Background Information — Summary of 2012 Annual Report 4 4.1 Facility History 4 4.2 Dewatering of Cell 2 4 4.3 Radon Flux Monitoring of Cell 2 4 4.4 Evaluation of Potential Factors Affecting Radon Flux 5 5.0 June 2014 Results 6 6.0 Other Information - Status of Proposed Updated Final Cover Design 6 7.0 Additional Information Required for Monthly Reports 7 7.1 Construction and Monitoring of Interim Cover Test Area, and Application of Additional Random Fill 7 7.2 Interim Corrective Action 8 8.0 Certification 9 2 1.0 Name and Location of the Facility Energy Fuels Resources (USA) Inc. ("EFRI") operates the White Mesa Mill (the "Mill"), located in central San Juan County, Utah, approximately 6 miles (9.5 km) south of the city of Blanding. The Mill can be reached by private road, approximately 0.5 miles west of Utah State Highway 191. Within San Juan County, the Mill is located on fee land and mill site claims, covering approximately 5,415 acres, encompassing all or part of Sections 21, 22, 27, 28, 29, 32, and 33 of T37S, R22E, and Sections 4, 5, 6, 8, 9, and 16 of T38S, R22E, Salt Lake Base and Meridian. All operations authorized by the Mill's State of Utah Radioactive Materials License are conducted within the confines of the existing site boundary. The milling facility currently occupies approximately 50 acres and the tailings disposal cells encompass another 275 acres. 2.0 Monthly Report Although Cell 2 is no longer in operation, this Report is being submitted as a monthly report for the Mill's Cell 2 for June 2014, consistent with 40 Code of Federal Regulations (CFR) 61.254(b) applicable to operating tailings impoundments. A summary of the events that gave rise to EFRI's decision to file this monthly report consistent with 40 CFR 61.254(b) is set out in Section 4 of this Report. A summary of the radon emissions from Cell 2 measured in June 2014 is set out in Section 5 of this Report. The monthly monitoring data for June 2014, consistent with 40 CFR 61.254(b), is provided in Attachment 1 to this Report, which contains the Radon Flux Measurement Program Report, dated June 2014, prepared by Tellco Environmental (the "Tellco June 2014 Monthly Report"). The results are summarized in Section 5 of this Report. 3.0 Name of the Person Responsible for Operation and Preparer of Report Energy Fuels Resources (USA) Inc. 225 Union Boulevard, Suite 600 Lakewood, Colorado 80228 303.628.7798 (phone) 303.389.4125 (fax) EFRI is the operator of the Mill and its tailings impoundments (Cells 2, 3, and 4A) and evaporation impoundments (Cells 1 and 4B). The Mill is an operating conventional uranium mill, processing both conventional ores and alternate feed materials. The "method of operations" at the Mill is phased disposal of tailings. The annual radon emissions for existing impoundments are measured using Large Area Activated Charcoal Canisters in conformance with 40 CFR, Part 61, Appendix B, Method 115, Restrictions to Radon Flux Measurements, (Environmental Protection Agency ["EPA"], 2008). These canisters are passive gas adsorption sampling devices used to determine the flux rate of Radon-222 gas from the surface of the tailings material. For impoundments licensed for use after December 15, 1989 (i.e., Cell 4A, and 4B), EFRI employs the work practice standard listed at 40 CFR 61.252(b)(1) in that all tailings impoundments constructed or licensed after that date are lined, are no more than 40 acres in area, and no more than two impoundments are operated for tailings disposal at any one time. Although Cell 2 is no longer in operation, EFRI is submitting this monthly compliance report consistent 3 with the standards in 40 CFR 61.254(b) applicable to operating tailings impoundments. 4.0 Background Information -- Summary of 2012 Annual Report 4.1 Facility History Cells 2 and 3, which have surface areas of 270,624 m2 (approximately 66 acres) and 288,858 m2 (approximately 71 acres), respectively, were constructed prior to December 15, 1989 and are considered "existing impoundments" as defined in 40 CFR 61.251. Radon flux from Cells 2 and 3 is monitored annually, as discussed below. Cells 4A and 4B were constructed after December 15, 1989. and are subject to the work practice standards in 40 CFR 61.252(b)(1), which require that the maximum surface area of each cell not exceed 40 acres. For this reason, Cells 4A and 4B are not required to undergo annual radon flux monitoring. Cell 4A receives the Mill's tailings sands. Cells 1 and 4B, receive solutions only, and are in operation as evaporation ponds. Cell 3, which is nearly filled, receives the Mill's solid waste and 1 le.(2) material only. Cell 2 is filled with tailings, is covered with an interim soil cover, and is no longer in operation. 4.2 Dewatering of Cell 2 The Utah Division of Water Quality issued Groundwater Discharge Permit ("GWDP") UGW-370004 in 2005. Under Part I.D.3 of the current GWDP, EFRI has been required to accelerate dewatering of the solutions in the Cell 2 slimes drain. Dewatering of Cell 2 began in 2008. In mid-2011, changes were made in the pumping procedures for slimes drain dewatering of Cell 2 that resulted in an acceleration of dewatering since that time. As discussed in more detail below, studies performed by EFRI indicate that the increase in radon flux from Cell 2 has likely been caused by these dewatering activities. No other changes appear to have occurred in condition, use, or monitoring of Cell 2 that could have resulted in an increase in radon flux from the cell. The average water level in the Cell 2 slimes drain standpipe for each of the years 2008 through 2013 indicate that water levels in Cell 2 have decreased approximately 3.98 feet (5600.56 to 5596.58 fmsl) since 2008. Of this decrease in water level, approximately 1 foot occurred between 2010 and 2011, reflecting the improved dewatering that commenced part way through 2011, and approximately 2 feet between 2011 and 2013, reflecting improved dewatering for all of 2012 and 2013. 4.3 Radon Flux Monitoring of Cell 2 Tellco performed the 2012 radon flux sampling during the second quarter of 2012 in the month of June. On June 25, 2012, Tellco advised EFRI that the average radon flux for Cell 2 from samples taken in June 2012 was 23.1 pCi/(m2 -sec) (referred to in the Tellco report as pCi/m2-s), which was higher than the 20 pCi/(m2 -sec) standard referred to in 40 CFR 61.252(a). The result of the 2012 radon-222 flux monitoring for Cell 3 was 18 pCi/(m2 -sec). Cell 3, therefore, was in compliance with this standard for 2012. The results of the 2013 Cell 3 radon-222 flux monitoring were discussed in the 2013 Annual Radon Flux Monitoring Report for Cell 3 submitted on March 27, 2014. 4 40 CFR 61.253 provides that: "When measurements are to be made over a one year period, EPA shall be provided with a schedule of the measurement frequency to be used. The schedule may be submitted to EPA prior to or after the first measurement period." EFRI advised the Utah Division of Air Quality ("UDAQ"), by notices submitted on August 3 and September 14, 2012, that EFRI planned to collect additional samples from Cell 2 in the third and fourth quarters of 2012. These samples were collected on September 9, October 21, and November 21, 2012, respectively. As the June 2012 monitoring for Cell 3 indicated that it was in compliance with the standard, further monitoring of Cell 3 was not performed in 2012. The result of the 2012 radon-222 flux monitoring for Cell 2 was 25.9 pCi/(m2 -sec) (averaged over four monitoring events). The measured radon flux from Cell 2 in 2012 was therefore higher than the standard of 20 pCi/(m2 -sec) referred to in 40 CFR 61.252(a). The Cell 2 and Cell 3 radon flux results were reported in EFRI's 2012 Annual Radon Flux Monitoring Report (the "2012 Annual Report"). The provisions of 40 CFR 61.254(b) requires that: "If the facility is not in compliance with the emission limits of paragraph 61.252 in the calendar year covered by the report, then the facility must commence reporting to the Administrator on a monthly basis the information listed in paragraph (a) of this section, for the preceding month. These reports will start the month immediately following the submittal of the annual report for the year in non-compliance and will be due 30 days following the end of each month." This report is being submitted as the monthly report for June 2014 for Cell 2, consistent with the requirements set out in 40 CFR 61.254(b). As mentioned in the cover letter, EFRI submitted a request to cease monthly sampling on May 30, 2014 with the April 2014 Monthly Report. On July 23, 2014 EFRI received approval from UDAQ and the Utah Division of Radiation Control to cease monthly sampling, and therefore, this will be the last monthly report submitted. Future sampling will be conducted in accordance with the requirements described in the July 23, 2014 letter. 4.4 Evaluation of Potential Factors Affecting Radon Flux In an attempt to identify the cause of the increase in radon flux at Cell 2, EFRI conducted a number of evaluations in 2013, including: • Excavation of a series of 10 test pits in the Cell 2 sands to collect additional information needed to ascertain factors affecting radon flow path and flux, • Evaluation of radon trends relative to slimes drain dewatering, • Development of correlation factors relating dewatering rates to radon flux, and • Estimation of the thickness of temporary cover that would be required to reduce radon flux to levels lower than 20 pCi/(m2 -sec), during the dewatering process. These studies and results are discussed in detail in EFRI's 2012 Annual Radon Flux Report and summarized in the remainder of this section. 5 Slimes drain dewatering data indicate that a lowering of the water level in Cell 2 has resulted in an increase in the average radon flux, and that an increase in water level has resulted in a decrease in the average radon flux. Changes in radon flux have consistently been inversely proportional to changes in water levels in Cell 2 since 2008. For the last three years the change in radon flux has been between 3 and 5 pCi/(m"-sec) per each foot of change in water level. It is also noteworthy that the significant increases in radon flux from Cell 2 which occurred between 2010 and 2011 and between 2011 and 2012 coincided with the periods of improved (accelerated) dewatering of Cell 2. EFRI has evaluated these results and has concluded that the increase in radon-222 flux from Cell 2 in excess of 20 pCi/(m2 -sec) is most likely the unavoidable result of Cell 2 dewatering activities mandated by the Mill's State of Utah GWDP. This is due to the fact that saturated tailings sands attenuate radon flux more than dry tailings sands, and the thickness of saturated tailings sands decrease as dewatering progresses. There appear to have been no other changes in conditions at Cell 2 that could have caused this increase in radon flux from Cell 2. These conclusions are supported by evaluations performed by SENES Consultants Limited ("SENES"), who were retained by EFRI to assess the potential effects of dewatering on the radon flux from Cell 2 and to provide calculations of the thickness of temporary cover required to achieve the radon flux standard during the dewatering process. SENES' evaluations were presented in a report provided as an attachment to EFRI's 2012 Annual Report. SENES estimated a theoretical radon flux from the covered tailings at Cell 2 for various depths (thicknesses) of dry tailings, and predicted future increases in radon flux as a function of decreases in water levels. In order to explore potential interim actions that could be taken to maintain radon flux at levels at or below 20 pCi/(m"-sec), the SENES study also evaluated the extent to which radon emanations from the cell can be reduced by increasing the thickness of the current interim cover on Cell 2. 5.0 June 2014 Results Detailed results for June 2014 for Cell 2 are contained in the Tellco June 2014 Monthly Report. As described in the Tellco June 2014 Monthly Report, monitoring was performed consistent with 40 CFR 61 Subpart W Appendix B, Method 115 radon emissions reporting requirements. The radon monitoring consisted of 100 separate monitoring points at which individual radon flux measurements have been made by collection on carbon canisters. The individual radon flux measurements were averaged to determine whether they exceeded 20 pCi/(m2-sec). The average radon flux for Cell 2 in June 2014 was reported by Tellco to be 15.0 pCi/(m2-sec). 6.0 Other Information - Status of Proposed Updated Final Cover Design As part of developing the Mill's final reclamation plan required to achieve the radon flux standard of 20 pCiy(m2-sec), a final engineered cover design was submitted by TITAN Environmental in 1996 and approved by the US Nuclear Regulatory Commission ("NRC"). An updated final cover design for the Mill's tailings system, submitted in November 2011, is under review by the Utah Division of Radiation Control ("DRC"), and is not currently approved. DRC provided a second round of interrogatories on the proposed cover design and associated Infiltration and Contaminant Transport Model ("ICTM") in February 2013. On April 30, 2013, a meeting was held in Denver, Colorado to discuss specific issues identified in DRC's February 2013 review comments, including, but not limited to, DRC's request for site-specific tailings 6 data and a probabilistic seismic hazard analysis ("PSHA") for the Mill. Representatives of DRC, DRC's consultant (URS Professional Solutions, LLC), EFRI, and EFRI's technical consultant (MWH Americas, Inc.) attended the meeting. During the meeting, EFRI proposed a tailings investigation to address the request for site-specific tailings data. A work plan for this investigation was provided to DRC on June 24, 2013, and DRC provided approval of the work plan verbally to EFRI on September 12, 2013. The tailings investigation was completed in October 2013 and subsequent laboratory testing of samples collected was completed in April 2014. A Tailings Data Analysis Report summarizing the results of the investigation is currently being prepared for submittal to DRC in June 2014. A PSHA for the Mill is being prepared for submittal to DRC in June 2014 as well. Submission of responses to DRC's February 2013 review comments on Revision 5.0 of the Reclamation Plan are planned to be completed in 2014 after DRC's review of the Tailings Data Analysis Report and PSHA for the Mill. The results provided in the Tailings Data Analysis Report and PSHA for the Mill will be used to update technical analyses to address DRC's February 2013 review comments on Revision 5.0 of the Reclamation Plan. The responses will also incorporate decisions made at the April 30, 2013 meeting on key issues related to Revision 5.0 of the Reclamation Plan. 7.0 Additional Information Required for Monthly Reports Controls or Other Changes in Operation ofthe Facility 40 CFR 61.254(b)(1) states that in addition to all the information required for an Annual Report under 40 CFR 61.254(b), monthly reports provided under that section shall also include a description of all controls or other changes in operation of the facility that will be or are being installed to bring the facility into compliance. Based on the evaluations described in Section 4, above, and as discussed during EFRI's March 27, 2013 meeting with UDAQ and DRC staff, in addition to the monthly monitoring reported in this Monthly Report, EFRI has performed the following steps to ensure that radon emissions from Cell 2 are kept as low as reasonably achievable and at or below 20 pCi/(m2-sec). 7.1 Construction and Monitoring of Interim Cover Test Area, and Application of Additional Random Fill i. EFRI constructed 12 test areas on Cell 2 to assess the effect of the addition of one foot of additional soil cover. EFR applied one foot of random fill moistened and compacted by a dozer to 12 circular test areas of approximately 100 to 120 feet in diameter. The total tested area is larger than the single 100 foot by 100 foot area proposed in previous Cell 2 monthly radon flux monitoring reports. Installation of 12 test areas containing the additional 1 foot of compacted soil was completed by August 2, 2013. Wetting and re-compaction of all 12 areas was completed prior to the start ofthe September 21, 2013 monthly flux monitoring event. ii. The radon flux has been monitored monthly at 100 locations on Cell 2, including the 12 test areas, since April 2013. iii. The effectiveness of the additional compacted cover at the 12 test areas was evaluated over several months. The additional cover on the 12 test areas was successful in achieving the desired reduction to 20 pCi/(m2-sec) or lower. As a result, EFRI applied additional random fill at 90% compaction to other areas of Cell 2 to further reduce the radon flux measurements. 7 Based on discussions with DRC, EFRI will proceed with the application of cover and will provide a letter to DRC with information demonstrating that the application of soil cover is consistent with the design and QC requirements of the proposed Reclamation Plan, currently under revision, on the understanding that the application of cover will be credited toward the final cover design. 7.2 Interim Corrective Action EFRI has taken the following additional steps to provide interim mitigation of radon flux from Cell 2. EFRI has identified the areas of elevated radon flux associated with known sources of radiological contamination at or near the surface of the cell cover. Specifically: • Windblown tailings from Cell 3 which have been deposited on Cell 2 as Cell 3 is being closed have been removed and re-buried in Cell 3. A berm approximately five feet high, extending the length of the Cell 3 beach has been constructed at the edge of Cell 2, to prevent further carryover of sands from Cell 3 onto the Cell 2 cover prior to closure of Cell 3. • Any contaminated material near the surface of Cell 2 has been reburied. • Additional cover material has been added to each of 12 identified areas of elevated flux on Cell 2. • Additional cover material has been added to other areas with elevated flux on Cell 2. • Monthly radon flux monitoring to assess the effectiveness of the above actions is ongoing. a) Facility's Performance Under Terms of Judicial or Administrative Enforcement Decree The Mill is not under a judicial or administrative enforcement decree. 8 8.0 Certification I Certify under penalty of law that I have personally examined and am familiar with the information submitted herein and based on my inquiry of those individuals immediately responsible for obtaining the information, I believe that the submitted information is true, accurate and complete. I am aware that there are significant penalties for submitting false information including the possibility of fine and imprisonment. See IMU.S.Gf. 1001. Signed David C. Fr^dSn Senior Vice Presidenjt, General Counsel & Corporate Secretary Date: ATTACHMENT 1 National Emissions Standards for Hazardous Air Pollutants 2014 Radon Flux Measurement Program June 2014 Sampling Results National Emission Standards for Hazardous Air Pollutants 2014 Radon Flux Measurement Program White Mesa Mill 6425 South Highway 191 Blanding, Utah 84511 June 2014 Sampling Results Cell 2 Prepared for: Energy Fuels Resources (USA) Inc. 6425 S. Highway 191 P.O. Box 809 Blanding, Utah 84511 Prepared by: Tellco Environmental P.O. Box 3987 Grand Junction, Colorado 81502 TABLE OF CONTENTS Page 1. INTRODUCTION 1 2. SITE HISTORY AND DESCRIPTION 1 3. REGULATORY REQUIREMENTS FOR THE SITE 2 4. SAMPLING METHODOLOGY 2 5. FIELD OPERATIONS 3 5.1 Equipment Preparation 3 5.2 Sample Locations, Identification, and Placement 3 5.3 Sample Retrieval 3 5.4 Environmental Conditions 4 6. SAMPLE ANALYSIS 4 6.1 Apparatus 4 6.2 Sample Inspection and Documentation 5 6.3 Background and Sample Counting 5 7. QUALITY CONTROL (QC) AND DATA VALIDATION 5 7.1 Sensitivity 6 7.2 Precision 6 7.3 Accuracy 6 7.4 Completeness 6 8. CALCULATIONS 6 9. RESULTS 7 9.1 Mean Radon Flux 7 9.2 Site Results 8 References 9 Figure 1 10 Appendix A. Charcoal Canister Analyses Support Documents Appendix B. Recount Data Analyses Appendix C. Radon Flux Sample Laboratory Data, Including Blanks Appendix D. Sample Locations Map (Figure 2) 1. INTRODUCTION During June 02-03, 2014 Tellco Environmental, LLC (Tellco) of Grand Junction, Colorado, provided support to Energy Fuels Resources (USA) Inc. (Energy Fuels) to conduct radon flux measurements at its White Mesa Mill site regarding the required National Emission Standards for Hazardous Air Pollutants (NESHAPs) Radon Flux Measurements. These measurements are required of Energy Fuels to show compliance with Federal Regulations (farther discussed in Section 3 below). The standard is not an average per facility, but is an average per radon source. The standard allows mill owners or operators the option of either making a single set of measurements to represent the year or making multiple measurements over a one year period (e.g., weekly, monthly, or quarterly intervals). Energy Fuels is presently performing radon flux measurements on a monthly basis at Cell 2. Prior to 2012, Energy Fuels had been making a single set of measurements to represent the radon flux each year; however, as the radon flux levels began exceeding the regulatory standard of 20 picoCuries per square meter per second (pCi/m2-s) in 2012, Energy Fuels responded by opting to make the radon flux measurements on a more frequent basis. Also, in response to the increase in the radon flux rates, Energy Fuels has placed approximately 19,432 cubic meters of additional material, varying in depth from approximately 31-61 centimeters, throughout an area of approximately 50,130 square meters (m2). In March 2014, Energy Fuels suspended the placement of additional cover materials at Cell 2 because the average flux rate had been below the regulatory standard for several months. Tellco was contracted to provide radon canisters, equipment, and canister-placement personnel as well as lab analysis of samples collected. Energy Fuels personnel provided support for loading and unloading charcoal from the canisters. This report details the procedures employed by Energy Fuels and Tellco to obtain the results presented in Section 9.0 of this report. This report presents the radon flux measurements results only for Cell 2 for June 2014; the results of the Cell 3 radon flux measurements for the second quarter 2014 sampling are presented in a separate report. 2. SITE DESCRIPTION The White Mesa Mill facility is located in San Juan County in southeastern Utah, six miles south of Blanding, Utah. The mill began operations in 1980 for the purpose of extracting uranium and vanadium from feed stocks. Processing effluents from the operation are deposited in lined cells, which vary in depth. Cell 1, Cell 4A, and Cell 4B did not require radon flux sampling, as explained in Section 3 below. Cell 2, which has a total area of approximately 270,624 m2, has been filled and covered with interim cover. This cell is comprised of one region, an interim soil cover of varying thickness, which requires NESHAPs radon flux monitoring. There were no apparent exposed tailings within Cell 2 during the June 2014 sampling. Cell 3, which has a total area of approximately 288,858 m2, is nearly filled with tailings sand and is undergoing pre-closure activities. This cell is comprised of two source regions that require NESHAPs l radon monitoring: a soil cover region of varying thickness and an exposed tailings "beaches" region. The remaining area is covered by standing liquid in lower elevation areas. 3. REGULATORY REQUIREMENTS FOR THE SITE Radon emissions from the uranium mill tailings at this site are regulated by the State of Utah's Division of Radiation Control and administered by the Utah Division of Air Quality under generally applicable standards set by the U.S. Environmental Protection Agency (EPA) for Operating Mills. Applicable regulations are specified in 40 CFR Part 61, Subpart W, National Emission Standards for Radon Emissions from Operating Mill Tailings, with technical procedures in Appendix B. At present, there are no Subpart T uranium mill tailings at this site. These regulations are a subset of the NESHAPs. According to subsection 61.252 Standard, (a) radon-222 emissions to ambient air from an existing uranium mill tailings pile shall not exceed an average of 20 pCi/m2-s for each pile (or cell). Subsection 61.253, Determining Compliance, states that: "Compliance with the emission standard in this subpart shall be determined annually through the use of Method 115 of Appendix B." Cell 1 is completely covered with standing liquid and therefore no radon flux measurements are required on Cell 1. The repaired Cell 4A, and newly constructed Cell 4B, were both constructed after December 15, 1989 and each was constructed with less than 40 acres surface area. Cell 4A and 4B comply with the requirements of 40 CFR 61.252(b), therefore no radon flux measurements are required on either Cell 4A or 4B. 4. SAMPLING METHODOLOGY Radon emissions were measured using Large Area Activated Charcoal Canisters (canisters) in conformance with 40 CFR, Part 61, Appendix B, Method 115, Restrictions to Radon Flux Measurements, (EPA, 2013). These are passive gas adsorption sampling devices used to determine the flux rate of radon-222 gas from a surface. The canisters were constructed using a 10-inch diameter PVC end cap containing a bed of 180 grams of activated, granular charcoal. The prepared charcoal was placed in the canisters on a support grid on top of a Vz inch thick layer of foam and secured with a retaining ring under VA inches of foam (see Figure 1, page 10). One hundred sampling locations were distributed throughout Cell 2 (consisting of one region) as depicted on the Sample Locations Map (see Figure 2, Appendix D). Each charged canister was placed directly onto the surface (open face down) and exposed to the surface for 24 hours. Radon gas adsorbed onto the charcoal and the subsequent radioactive decay of the entrained radon resulted in radioactive lead-214 and bismuth-214. These radon progeny isotopes emit characteristic gamma photons that can be detected through gamma spectroscopy. The original total activity of the adsorbed radon was calculated from these gamma ray measurements using calibration factors derived from cross-calibration of standard sources containing known total activities of radium-226 with geometry identical to the counted samples and from the principles of radioactive decay. After approximately 24 hours, the exposed charcoal was transferred to a sealed plastic sample container (to prevent radon loss and/or further exposure during transport), identified and labeled, and transported to the Tellco laboratory in Grand Junction, Colorado for analysis. Upon completion of on- site activities, the field equipment was alpha and beta-gamma scanned by Energy Fuels Radiation Safety personnel for possible contamination resulting from fieldwork activities. All of the field equipment used was subsequently released for unrestricted use. Tellco personnel maintained custody of the samples from collection through analysis. 2 5. FIELD OPERATIONS 5.1 Equipment Preparation All charcoal was dried at 110°C before use in the field. Unused charcoal and recycled charcoal were treated the same. 180-gram aliquots of dried charcoal were weighed and placed in sample containers. Proper balance operation was verified daily by checking a standard weight. The balance readout agreed with the known standard weight to within ± 0.1 percent. After acceptable balance check, empty containers were individually placed on the balance and the scale was re-zeroed with the container on the balance. Unexposed and dried charcoal was carefully added to the container until the readout registered 180 grams. The lid was immediately placed on the container and sealed with plastic tape. The balance was checked for readout drift between readings. Sealed containers with unexposed charcoal were placed individually in the shielded counting well, with the bottom of the container centered over the detector, and the background count rate was documented. Three five-minute background counts were conducted on ten percent of the containers, selected at random to represent the "batch". If the background counts were too high to achieve an acceptable lower limit of detection (LLD), the entire charcoal batch was labeled non-conforming and recycled through the heating/drying process. 5.2 Sample Locations, Identification, and Placement On June 02, 2014, 100 sampling locations were spread out throughout the Cell 2 covered region. The same sampling locations that were established for previous samplings of Cell 2 were used for the placement of the canisters, although the actual sample identification numbers (IDs) are different. An individual ID was assigned to each sample point, using a sequential alphanumeric system indicating the charcoal batch and physical location within the region (e.g., 101...1100). This ID was written on an adhesive label and affixed to the top of the canister. The sample ID, date, and time of placement were recorded on the radon flux measurements data sheets for the set of one hundred measurements. Prior to placing a canister at each sample location, the retaining ring, screen, and foam pad of each canister were removed to expose the charcoal support grid. A pre-measured charcoal charge was selected from a batch, opened and distributed evenly across the support grid. The canister was then reassembled and placed face down on the surface at each sampling location. Care was exercised not to push the device into the soil surface. The canister rim was "sealed" to the surface using a berm of local borrow material. Five canisters (blanks) were similarly processed and these canisters were kept inside an airtight plastic bag during the 24-hour testing period. 5.3 Sample Retrieval On June 03, 2014 at the end of the 24-hour testing period, all canisters were retrieved, disassembled and each charcoal sample was individually poured through a funnel into a container. Identification numbers were transferred to the appropriate container, which was sealed and placed in a box for 3 transport. Retrieval date and time were recorded on the same data sheets as the sample placement information. The blank samples were similarly processed. All 100 charcoal samples from Cell 2 covered region were successfully retrieved and containerized during the retrieval and unloading process. Tellco personnel maintained custody of the samples from collection through lab analysis. 5.4 Environmental Conditions A rain gauge and thermometer were placed within Cell 2 to monitor rainfall and air temperatures during sampling; additionally, Energy Fuels maintains an onsite rain gauge. In accordance with 40 CFR, Part 61, Appendix B, Method 115: • Canisters were not placed within 24 hours of rainfall at the site. • There was no rainfall at the site after the placement of the canisters. • The criteria regarding minimum ambient air temperature and frozen ground do not apply when performing sampling on a monthly basis; however, the minimum air temperature during the sampling period was 48 degrees F, and the ground was not frozen at any of the sample locations. 6. SAMPLE ANALYSIS 6.1 Apparatus Apparatus used for the analysis: • Single- or multi-channel pulse height analysis system, Ludlum Model 2200 with a Teledyne 3" x 3" sodium iodide, thallium-activated (Nal(Tl)) detector. • Lead shielded counting well approximately 40 cm deep with 5-cm thick lead walls and a 7- cm thick base and 5 cm thick top. • National Institute of Standards and Technology (NIST) traceable aqueous solution radium- 226 absorbed onto 180 grams of activated charcoal. • Ohaus Model C501 balance with 0.1 -gram sensitivity. 4 6.2 Sample Inspection and Documentation Once in the laboratory, the integrity of each charcoal container was verified by visual inspection of the plastic container. Laboratory personnel checked for damaged or unsealed containers and verified that the data sheet was complete. All of the 100 sample containers and 5 blank containers received and inspected at the Tellco analytical laboratory were ultimately verified as valid and no damaged or unsealed containers were observed. 6.3 Background and Sample Counting The gamma ray counting system was checked daily, including background and radium-226 source measurements prior to and after each counting session. Based on calibration statistics, using two sources with known radium-226 content, background and source control limits were established for each Ludlum/Teledyne system with shielded counting well (see Appendix A). Gamma ray counting of exposed charcoal samples included the following steps: • The length of count time was determined by the activity of the sample being analyzed, according to a data quality objective of a minimum of 1,000 accrued counts for any given sample. • The sample container was centered on the Nal gamma detector and the shielded well door was closed. • The sample was counted over a determined count length and then the mid-sample count time, date, and gross counts were documented on the radon flux measurements data sheet and used in the calculations. • The above steps were repeated for each exposed charcoal sample. • Approximately 10 percent of the containers counted were selected for recounting. These containers were recounted on the next day following the original count. 7. QUALITY CONTROL (QC) AND DATA VALIDATION Charcoal flux measurement QC samples included the following intra-laboratory analytical frequency objectives: • Blanks, 5 percent, and • Recounts, 10 percent All sample data were subjected to validation protocols that included assessments of sensitivity, precision, accuracy, and completeness. All method-required data quality objectives (EPA, 2013) were attained. 5 7.1 Sensitivity A total of five blanks were analyzed by measuring the radon progeny activity in samples subjected to all aspects of the measurement process, excepting exposure to the source region. These blank sample measurements comprised approximately 5 percent of the field measurements. Analysis of the five blank samples measured radon flux rates ranging from approximately 0.06 to 0.09 pCi/m2-s, with an average of approximately 0.07 pCi/m2-s. The lower limit of detection (LLD) was approximately 0.04 pCi/m2-s. 7.2 Precision Ten recount measurements, distributed throughout the sample set, were performed by replicating analyses of individual field samples (see Appendix B). These recount measurements comprised approximately 10 percent of the total number of samples analyzed. The precision of all recount measurements, expressed as relative percent difference (RPD), ranged from less than 0.1 percent to 8.0 percent with an overall average precision of approximately 2.8 percent RPD. 7.3 Accuracy Accuracy of field measurements was assessed daily by counting two laboratory control samples with known Ra-226 content. Accuracy of these lab control sample measurements, expressed as percent bias, ranged from approximately -2.0 percent to +0.5 percent. The arithmetic average bias of the lab control sample measurements was approximately -0.5 percent (see Appendix A). 7.4 Completeness All 100 of the samples from the Cell 2 cover region were verified, representing 100 percent completeness. 8. CALCULATIONS Radon flux rates were calculated for charcoal collection samples using calibration factors derived from cross-calibration to sources with known total activity with identical geometry as the charcoal containers. A yield efficiency factor was used to calculate the total activity of the sample charcoal containers. Individual field sample result values presented were not reduced by the results of the field blank analyses. In practice, radon flux rates were calculated by a database computer program. The algorithms utilized by the data base program were as follows: Equation 8.1: , N pCi Rn-222/rrrsec = [Xs*A*b*0 5(*"i is^ 6 where: N = net sample count rate, epm under 220-662 keV peak Ts = sample duration, seconds b = instrument calibration factor, epm per pCi; values used: 0.1699, for M-01/D-21 and 0.1702, for M-02/D-20 d = decay time, elapsed hours between sample mid-time and count mid-time A = area of the canister, m2 Equation 8.2: I Gross Sample, epm Background Sample,epm + ySample Count,t,min Background Count,t,min Error,2a = 2x x Sample Concentration Net,epm Equation 8.3: TTn_ 2.71+(4.65KSh) LLD_ [Ts*A*b*0.5(d/9T75)] where: 2.71 = constant 4.65 = confidence interval factor Sb = standard deviation of the background count rate Ts = sample duration, seconds b = instrument calibration factor, epm per pCi; values used: 0.1699,forM-01/D-21 and 0.1702, for M-02/D-20 d = decay time, elapsed hours between sample mid-time and count mid-time A = area ofthe canister, m2 9. RESULTS 9.1 Mean Radon Flux Referencing 40 CFR, Part 61, Subpart W, Appendix B, Method 115 - Monitoring for Radon-222 Emissions, Subsection 2.1.7 - Calculations, "the mean radon flux for each region of the pile and for the total pile shall be calculated and reported as follows: (a) The individual radon flux calculations shall be made as provided in Appendix A EPA 86(1). The mean radon flux for each region of the pile shall be calculated by summing all individual flux measurements for the region and dividing by the total number of flux measurements for the region. (b) The mean radon flux for the total uranium mill tailings pile shall be calculated as follows: JIAI + .. . J2A2 r+i. .. JA, Js = A, Where: Js = Mean flux for the total pile (pCi/m2-s) J, = Mean flux measured in region i (pCi/m2-s) Aj = Area of region i (m2) At = Total area ofthe pile (m2)" 7 Figure 1 Large Area Activated Charcoal Canisters Diagram Hinttl* 1/4 iiu Vent Hoi* I-in Tmcli i Strubfaur Pid i^rutxiiii Pi 3 1 '2 Ttiic» C>i«rck>fl. Ruuin*r 1 rvC En* C*p F]GtfltC 1 Laro.t-Ar»i Ititfon Collector 10 Appendix A Charcoal Canister Analyses Support Documents A CD < OT 52 2 CL < < o J 2 CM o < -J 111 O CO O LU Z O Q ^ z o3 co co UJ a: co co UJ UJ or CO < UJ X 13 o a ^2 LU D LL in CL < I CO LU Z ™ co o $ CN O CO CO LU I— < Q O Z L- f <=> UJ < CN O CO o o 8 a. cn in 5 O O ^ LL Q O LU Z E < c 3. o O cu o 3 o CO - CN E * m — * c ZJ O CD LU co5 CO If) d o CO o h- d CN CO If) d o oo If) CD If) co co o o in CN o CM CD CO CD CO CM O CO CM If) If) CM Q CM I a CM O If) O i CO o o CO z o co co LU CO I < o r-> < z < < ct o LL CO < CO I-z LLI o cr LU CL LU (D LU > < co O CM co CM o CHARCOAL CANISTER ANALYSIS SYSTEM SITE LOCATION: W W\T^ \K*^1 pAU\ , "&lftH<hwj > UT CLIENT: E"grg|Vj "Pu.-lU ^ e^O^CtS, C^ft Calibration Check Lop System ID: Calibration Date: Due Date: Scaler S/N: 5^ I 5 "7 ^* High Voltage: 10'2-5 Window: 4.42 Thrshld: 2.20 Detector S/N: 0 M 3 3 Source ID/SN: Source Activity: Blank Canister Bkgd. Range, epm: 2 a = _ Gross Source Range, epm: .to. to IS1/ .3a = _ OS47 3a = 9(^12- .to. to 11 I 012.8 Technician: All counts times are one minute. Pr-e- Date By Background Counts (1 min. each) #1 #2 #3 Avg. #1 Source Counts (1 min. each) #2 #3 Average ok? Y/N X5I L3& loi 3 3? MIME. iW t0O(7)O 1 00.-2-0 -¥- Y/N: Y = average background and source epm falls within the control limits. N = average background and source epm does not fall within the control limits. The acceptable ranges were determined from prior background and source check data. CHARCOAL CANISTER ANALYSIS SYSTEM SITE LOCATION: CLIENT: £-VV&»^y FvieU *R*£OWTcfS (^KS>S) Calibration Check Log System ID: rA ~ ° * / ~ Calibration Date: Q / If))?) Due Date: (*/ / ¥ / I V~ Scaler S/N: I S'l 0~ High Voltage: ( O 2-5 Window: 4.42 Thrshld: 2.20 Detector S/N: O 4~ 1 S 3 3 Source 1D/SN: Source Activity: 5°)>3K p C I Blank Canister Bkgd. Range, epm: 2 a = B 4? to I S" f 3 a = 6> ^ to 1 "7 / Gross Source Range, epm: 2q= 96^)5 to \os\^> 3fJ= o^lHO to jOUn\ Technician: ^f"— All counts times are one minute. Date By UUM ^VfT^o Background Counts (1 min. each) #1 #2 7W #3 Avg. #1 Source Counts (1 min. each) #2 #3 Average ok? Y/N 131 O 1^-i IQIS1 HI I4S" t^ff4 \ 3^ inn. IK I0\°)3 ±0^91 I0lg4 >33 J2i Y/N: Y = average background and source epm falls within the control limits. N = average background and source epm does not fall within the control limits. The acceptable ranges were determined from prior background and source check data. CHARCOAL CANISTER ANALYSIS SYSTEM SITE LOCATION: VAj^t-T^ TA-«Hc\ \A\ W ) ~R 1 gvK) jM T CLIENT: ^ VH.n^\j F\A.-eU R^QiAfUS n) Calibration Check Lop System ID: fr° 'Z/r)-2^ Calibration Date: U j 14 / 13 Due Date: C*//4/ I *•/ 5^5 Co3 High Voltage: / Q~l S Window: 4.42 Thrshld: 2.20 Detector S/N: (9 H 15 3"3- Source ID/SN: Source Activity: Sfy^Kpl. Blank Canister Bkgd. Range, epm: 2 a = _ 7 # to I5< 3o = GO to Scaler S/N: I7C7 Gross Source Range, epm: 2a = 995°) to \OS?-7 3o = 90 17 to \Q(*lf°> Technician: ^ O^DO^' All counts times are one minute. Date By Background Counts (1 min #1 #2 #3 each) Avg. #1 Source Counts (1 min. each) #2 #3 Average ok? Y/N 1QQ67- I 4 t 5H IE 3t? -53 )H3 COCK7 1 r7/ier 17^3 t3> Y/N: Y = average background and source epm falls within the control limits. N = average background and source epm does not fall within the control limits. The acceptable ranges were determined from prior background and source check data. CHARCOAL CANISTER ANALYSIS SYSTEM SITE LOCATION: CLIENT: £y\ef^y ^weU £eSouorc^ Q^S/f) Calibration Check Log System ID: °X/VCalibration Date: *f / I 3 Due Date: ) TV > 4 Scaler S/N: 5 ^ ^3 High Voltage: > Q"7^> Window: 4.42 Thrshld: 2.20 Detector S/N: ° H 1 5 3 2- Source ID/SN: Kq^/^S "Pfp Source Activity: S^.^Kp Blank Canister Bkgd. Range, epm: 2 CT = _ "7 3 to (5) 3CT= GO to I7C> Gross Source Range, epm: 2CT= to lonqg 30*= 9^63 Technician: \j/^T/^^ to All counts times are one minute. Date By Background Counts (1 min. each) #1 #2 #3 Avg. #i 5 Source Counts (1 min. each) #2 #3 I Average ok? Y/N 2 mm Sfc 034-0 ^7 9 V3 13 H4f5 1 Ot P-7 ipg-34 (*/&/'T TH 130 Y/N: Y = average background and source epm falls within the control limits. N = average background and source epm does not fall within the control limits. The acceptable ranges were determined from prior background and source check data. BALANCE OPERATION DAILY CHECK Balance Model: OKaM^ Pgrt-P-yS.U,: 1*23 °7 Standard Weight (g): Date Pre-check (g) Post-check (g) O.K. ± 0.1 % ? By 7-Oc?. o -2-00,0 -2~oc>, o Appendix B Recount Data Analyses B CD O o o O LU o CC Q_ < CO LLI X LU CC =3 co < LU O Q O Dl CL CO LU O cc 3> o co LU cc co >-o cc LLI _1 o cc < UJ —I o cc cn CNI CD LU CC < oo m _J < O o cc < o o 1 < 9= ^ Q cc 00 < a UJ > UJ cc x— ^? o S i a LU LU 2* LU < LL CC CM ZD CO co CQ o o o csi Q _ Q . . LU X >- < 0-m LU Q cc LU > O o co •<-o CM o" —I o o • 2 q o co x^ O O LU ^ CM . . • • < LU UJ • =! cc ty o CL < U_ O —I 3 m r- rH cn — co >- < cc LU I— co -z. < CJ o o LU cc in o LD 00 in mm mm mm mm mm mm oo oo oo oo oo oo m in o o m m o o m m o o oo oo oo oo oo oo cn cn co co <4"m H H r~ r- mm CNCN CN CN r-HH OO OO H H CO GO o o CN CN O O o o io o CN in rH cNm ko in oi o •*m H rH kD kD CNm CO CTl CO o CN CN CN CN CN f CO CO rH O CN CN l> CO kD kD CNCN mm mm oo mm CN CN rH mm o o mm CNCN CNCN CNCN CN CN CNCN CNCN CNCN CNCN CNCN CNCN CNCN CNCN mcN r- m cn CN ko r- r-mcs rH mm mm rH c- ^ o C- rH rH cn mm CN rH ^ CN CN m <tf CN CN CN CN CN CN ^ 00 ^ CO m co m CN co CO CN CN CN CN m m CTl CN CO kD m m CN CN CN CN r- H m u> r» m CN CN o m co m in CN m CN ko r- r- co cn in m CN H CN CN CN m CN m >^m mm mm mm mm ko r~ h ko r- ko r- ko r- r- ID kD kD 10 kD kD kD kD kD kD m m m m oooo coco coco r~ t- COCO coco mm CNCN •^•^ co co CNCN CNCN mm mm mm r~r~ oooo r- r~ r- r~ coco oo oo oo oo oo oo rHH CNCN mm mm ID ko m rH m rH rH kD r- kD kD kD kD CN CN kD kD CN CN m CN m m m m ko m rH H O O r- o o o CO oo o o CTl CTl o o CN CN O O m m o o H H o o m m o o kD kD o o r- r- H H o o oo co o o cn cn m m o o kD CN rH m m oo ^ H m kD r- io h kD r- k0 kD kD kD kD kD CTl CTl GO CO CO CO H rH rH rH CN CN CO CO CO CO CO CO cn CTI mm oo oo H H CN CN mm oo oo oo oo oo oo o o o o o o o o Appendix C Radon Flux Sample Laboratory Data (including Blanks) c o CD ininininininininLnininininininLninininininininmLnmm ooooooooooooooooooooooooooooooooooooo ooooooooooooooooooooooooooooooooooooo co o o o LU —3 o CC Q_ 9 o or < o or LU cc < § 8- l<l(^lnoHHn^NmI<^HOlnHU)lNo^nal^llIl^o(Ilr^a)•^ri^f^(l/)^Ill^lOMoo OOOCNOOOHOCNCN^rOHrHOrHrOrOCNiHCNTHrHrMOrHrHCNrHr^ ln(^nooomol^(^l)^Il'l|^n(^)l^lH^(^M^^^^t|o^lJll^loD^^M^^(^fl/l^ll)o ^l^^oHHr^u)N^)(NHOl/lo^fn^lHllO(N^^o(OH^nof*'^|^olllo^^^ CN H CN CN ^ rO rH H HnrOCNrHCNrHrHCN rH rH CN rH CN CN CN d rH lnc«(^)colfllIl(NH^^lal'^<f^o^t'flNnnl/)^^lH^H^fl0^l)^llln(^lnalHl/^lI)0 o(N^NcnHM^^l/)m^^olnnln(nmlnMcoo(^l^oc1(tnncDHulNl/l^o1Hl»l NMHMHNMMHMHMMNMC»l(\|NlNO)HMHPiHHO)MHMMrN(NP)N(NM CNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNM < CO LU CO CC co < =3 o Q O LU O CC Q_ CO LU O CC ZD o co LU CC CO I LU zz> U_ >-o cc LU co -3- CD ca < O o cc < >-m >-cc o UJ < i— < CC °° < a LU > UJ cc Lu o < Ll- CC CM ZD CO O CO —I • • a LU > a co < o =3 o o o CN Q CN LU _ a .. LU x >- < Q. CO UJ a cc LU > o o CN . . LU Qj =! CC co -r- O CN cf ^ —I o Q 2 o • 2 q CO > CO CD a z —I ZD LU O ko CN cn CN LO CN H OJ ^ rH n rH t^mcokc^inincfiinkoc'iiii o^co^cocoLficricor-cNLn ooocNt^oncnmcrirHn (OHHHlDHHC0U)H\O^ I—I H rH CNCNrHrHrHHrHH >iocooi^oioooiom<fn(N^o(Naco-jij)o rHr^CNinrHCNCNCNinOCTit^CNminoOCNin^OO OlCDinmrHCOITvCnOror^CnincNt^kDCOkOCNrHr^rH rH^CNCNrH^OU)^HrHU5LncOLncn<TiCNCNOOCNC-- n m ^J1 'J* 'st1 r~ cn cn *xl* ^J1 *f o o CN CN ro n in m in in in in in in in ko vo co co cn cn in m in in in in in HrHCNmininr-r~coco a) tr rH .f^^^Tf^if^^^^jji^ij^^^^-f^tf^ininuiiiiiniflmwi/ii/iuiiiiiiii/ii/i ^* rHrHr—Ir—Ir-Hi—Ir—IrH ^* H H H H rH rH rH kD kD kD kD kD VD kD kD kD kD kD kD kD kD in kD t- in in in CD cn in m ocNmi^inkDt^r-oocri ^* ^* ^* rHrHrHrHrHHi-HrHrHrHi-trHHrHrHrHHrHrHHrHrH kDkDVDkDkDkOkOkOkDkOkDkDkDVDkDkOkOkDkDkDkOkD kOkOkDkDkDkDkDkDkDkDkOkDkDVDkDkDkDkDkDkDkDkO OOHNMHO-.-.n,. ,on01II<ll ^^^^^o3(DIomo5CDII)c<loo(I)a)(I)cocox(^la)ooo)o^cooococo(^)col!oa)a)^^^ CO CTl rH m ro CN in ko co 'vt1 ^ ^ o m in in in in in c^[^r~r~[^[^[^[^-r-r^r^[^oococo ,--^OCNCNOm.n^^, ^COkD^CNOCOkOLTl^CN mt^a,HrHrHrHc0U3T,,cx,oininininin^^^^^ COC0CDCOC0COCDCDC0C0 00CDI>t~l>t^t^t^[^l>t~[^ HNPixfinkOhoooio OOOOOOOOOrH CNrO^inkDt^CDcnoHCNrO^inkOC^CDaiOrHCNrO^inkOt^ rHrHrHHHrHrHrHCNCNCNCNCNCNCNCNCNCNrOrOrornrOmrom HHHHHrHHrHHHrHrHMHrHrHHrHHHHHHHHH HCNn^inkDi>cocno OOOOOOOOOH rHrHHrHrHrHrHrHHH CNr0^inkDI>aD0^OrHCNrn^inkDr-CDCTlOrHCNm'^LnkDt-~ rHHHHHrHrHHCNCNCNCNCNCNCNCNCNCNC^romrOrOrOrOrn MMMHHMHHHMMMHHMHHMHI—IHHrHrHrHrH cb cb <=>. CNJ g CT> ^ CNI I LO LnuimLnLniriininLniriLnLninLninL^ I o oooooooooooooooooooooooooooooooooooo lo oooooooooooooooooooooooooooooooooooo CO o o o o CL 05 cc < LLI I o cc LU X cc < E CL CJ |H(IlH(NHH(tri^n^o^NOl^Il^I)^^^fOlnon^^||^«^op|(J^t|Kll^)l,)(I^^Il^Il I O CNOOOOLricnO^VOrHOHOOCNOVDnrHrHrHOOOM'rHnCNOOOCNnHO n ncNvocNt^nco^ocncnvocnncncn^i^r^n^cncNLncDCNcnocD |HcriHrHHOcooi^r^koaicoHCTiLnm^m<TiLnocN[>m CN LT) 01 •# V0 rH CN VD CN rH H rH >f n O) IN ro H co I CTl HOfflOd)(IlOa)01IN01vJMH)t/)(N>(Dl/IPIHvJll0riOOOOClPIHOHOOH I CN ^naiLnn^^rHocncoonvDC^^LnoinocnncNLncnvDOrHrHOrHcNooovD MNMHHCSMINNNMN(NtNHMMHN(NNHMMMHHMC«lrSNC>IMMMrNH ICNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNCNM < co co LU cc co < CO S3 < >-O to 0 >-% cc O Lu < 1— < cc 00 < ico ml^l^^^Mlflo1^(n^^^^llnric^mr^^f^^^t^MHont•n^Il(DO)^tn<Iln^^ In riU1lflno^olmlno^cflH^a^tm^ol^s^o)^^^tlNnal(^llI)oH(«l^fmnnlIl In ^OMlnr^Hml/)oolNOl^^r-^t(^lcocIl^I)OHH()lU)^l)'fOl^rllIl^Of<)0'fv«1| iHHHriHHMI/lniOlOnM^mMOriNfd^xflllMHriainrjOHINnmilllCOl rH CN CO rH CN rH CN rH rH rH rH rH ICNrHCNCNCNmrHH |vf^o^oon^Nlnlrl^^oa)alOlOlriH(NM^f^fLOl/l^^clJcoooHHn^1^f^ll^Il^o <p linLnuiiiiLniiiLriiriininLnininLnmLriL^ IrHrHrHrHHrHHrHrHHHrHrHrHrHrHrHrHrHrHrHiHrHrHrHrHrHrHHrHrHrHrHrHrHrH X ZD o a < cc o LU CD cc CL CO LU o cc o co LU cc CO >-CD cc LU o _l a > LU cc LU TJ- O T-< LI-CC CNI ZD CO co ZD Q < o o o CNI Q CN O X o I— _l < CL m LU a Q UJ o co •<- —I o a • : 5 LU o co O CD I ^J* ^* ^Jf ^* NJ* ^< ^* ^* %TJ* ^* *^ v"J< ^< ^< ^* ^* rHrHHrHrHHrHHrHrHrHHrHrHrHrHrHrHrHHrHrHrHrHrHrHrHrHrHrHrHrHrHrHHrHrH |vDVOVOVOVDVDVDVDVOVDVDVOVOVDVOVOVOVDVDVOVOVDVOVDVOVDVDVOVDVDV^ I VD VDVDVDVOVDVOVOVDV0VDVDVOV0VDVDVDVDVDVD ^tOlI)lfl^^mmnn,Mmrtl. .n..m.OHa^l^lmoHlNn^•lJlll)^I)(IlO I r^C^C^C^C^t^l^COCOCOCDCDODCDCOCOCDCOCDCOCDCOCOCOCDrom I rH cn(^)mmHM^fvo^cnoM^fvooon ^mOM^f^^(BmHc^^^^lfl^oal0^o^^ Ivfnnmn^^vfvt^vfi/iiiiiJiwin ^ HHHHHHdMMMriiNMiNnn j t> ^^^^^^^^^^^^^^^co(locomflococooococol3)mctla)cocococococ(loo 00 moriMM*iii»3>co<riOHMnsfiJivo[sa)moHPii<i*i/ivo>a)moHr<mvf n n^t^J^t^f^l'*^f^l|^f^l|lnlflllllIlllllnlnullnln^ovo^o^fl^^Ilu^tl^I)^l)^^^^^ |M HHMHHHMMMHHHMHHMMMMHHHHHHHHHMHHMHMHHM Ico lIlOHf^n^)Ul^o^lIl(llOHr^n^fln^I)^a)moriPln^!lfl^o^^IOlOHf^n'J |n n^f^f^•^f^^«^^^<'l/)lnl/llnl/)lI1l/lUll/)l^lvo^D^JU)^Il^l)^^^I)lo^I)^^^^^ HHrHHHHHHHHHMHHHrHHHHHHMHrHHrHHHHHHHHHHH . . < O Z LU LU —I ZD _! o; yj o CO o o o o UJ o re CL < co ZTZ co" I— -z. LU LU CC ZD CO < X ZD o a o LU —D o cr: CL co LU o cc ZD o co LU Ql CO >- CD cr: LU O 05 cr: < LU —I O 01 < E CL CJ CO £0 «a < >-O £0 0 >-LL cr: ft CO T t ^ o g I < £= Q < a LU > LU CC O CD Q iii LU o < LL DC CM ZD CO ZD >- Q CD a <| LU o o o o CNI Q CNJ O _ Q . . LU ZC >- ^2 < CL m LU Q DC LU > O o CN . . • • < LU LU =! CC CL < CO T- Og ci i= —I o o • 5? LU O CO O CD —I ZD LU O LL O a -H PH o H inmuiinuiiiii/ii/iini/iini/ii/iiiiiiii/ii/iifiiiiini/iuii/iini/iir 00000000000000000000000000 00000000000000000000000000 nHri^p|ul^^nu)o^l'^H^^^^DO\nHH^lnHM OOOOOOOrHrHOOrHOHCNOOOOOOOOOOO i/iHitniiirimuiiNUiiNcoiiioioir-Mco^ion'jor'HU) rOOJ^kO^CNUlCAvffflOvOMlillTlMHOOJMrHH rH H H IN c^mlnmv0^oHcncnm^fCN^o(NM<t|l^lOHco^fc,^cfl^ooo ^Huimncoinui^NH^'joni'iooifuiHciioaiin'i1 HNMMINCNPlINrNPIOgOIOiNMCNMrNltNtNINHHrilNH | CTl H(»Nnnr-Ori>f^«)t3ri(Iltsl/l!IlHOia)0\CD^>sf In st>oomtocim(NuiiNtoiNonooovDNO'#oiiiiinM io ainnir)cDHLni>rHrHcTicnincNi^on[^HncNt--HrHLn in HrHrHrHHCNVOVDHCNnrHLnCOCNrHCNnrHrHrHHrHrHrH HCNnCNrHCNrHrHrHrHH HHHtNsfNHMtN r>cOrHHnLnt>i>cricTi Kj< vjinuiininininuiiii oocNCNnnininvovocri rH LO ^ GO CO I LD ininiiiuiinininiiiirkoiBiflWkOvOiDkOkouivOiokDLoujii) HrHrHrHHrHHHHrHrHHrHi-lrHrHrHrHrHrHrHrHrHrHrH I ^P ^* ^J* ^* ^* ^* 'NF ^* ^* *^ ^* ^* rHrHrHHrHHrHrHrHrHrHHrHrHHrHHHrHrHrHrHrHHrHrH |vDV0VOVDVOVDVDVDVDV0VDVDVDVDVDV0V0V0VOVDVOVOV0VOVDVD I >H r^^Il^o)mlJlOHN^fI^l^o^^^)(^oHr^n^«lI1^^^co In nrlrlHHHOIt>lPIN(NM(NHHHPiMNriMMNDIN I CO COCOCOCOCOCOCOCOCDCOCOCDCDCDCOCOCDaOCDCDCOCDCOCOCO In ^^vooocTirHnLni^ocNn^on^voi^cTiocNninvDco in nrHHHHCNCNcNCNnnnncNCNrNicNOJCNnnnnnn IcO COCOmcDCOCOCOOOCOCOCDaDCDCOCOCOCOCOCOCOCOCOCOCDCO in vor>cocTioHCNn^invo[^cDCTiOrHCNn^LnvDi^cDcTi:r: I r- i^t^t^t^cocococooococDCDCDcocTicTicncTicTic^ IrHMHrHHHHHHHHHMMHHHHMHHHHHrj m^l)^a)moHo^n^^L^^^^oDmoHtNn^fln^D^(^)Ol 11> ^^^^(X)cocococD(^)oomcococ^c^mc^wo1mmc^c^l HMHHHHHHHHHHHHHHHHrHrHHMHH J J hi J J OOOOO fr! pi pi Pi Oi tH E-I H H E-I a a 2 s a ooooo CJ CJ u u u ^* ^* ^* ooooo ^3 co o o CO — CO >- < cc LU — < m ooooo n n n n n ooooo ooooo VO r- CO VO 01 ooooo ooooo CO CTl O n rH CTi CTi CTi 000 CN CN CN CN CTl CTi f- CN VO VO O rH CTl H O CN CN LO 00 co 01 vo r- OOOOO VO VD C- [~- CO rH H CN CN n OOO rH rH rH *si* ^i* VD VD VD VO VD VD VO VO VD VD OOOOO 00 00 CO CO CO in in in in LD CN CN CN CN CN r- r- r- r- r- H CN n ^ m ^ ^ ^ m pq PQ pq pq tH M H HH H rH CN n in r^ r^HI r^ r^ M J J J J pq pq pq PQ pq Appendix D Sample Locations Map (Figure 2) D I h- Z Q Z < < X z n "3- < ^ 2 o ass w 5 s si L73 • £3. HQ vnQ XDQ r,0 ?:0 0 a