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AMBIENT AIR MONITORING PROGRAM MUGGAH CREEK REMEDIATION PROJECT FEBRUARY 2003 SAMPLING EVENTS FINAL REPORT

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AMBIENT AIR MONITORING PROGRAM MUGGAH CREEK REMEDIATION PROJECT

FEBRUARY 2003 SAMPLING EVENTS

FINAL REPORT

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AMBIENT AIR MONITORING PROGRAM MUGGAH CREEK REMEDIATION PROJECT

FEBRUARY 2003 SAMPLING EVENTS

FINAL REPORT

SUBMITTED TO:

NOVA SCOTIA DEPARTMENT OF TRANSPORTATION AND PUBLIC WORKS C/O CONESTOGA-ROVERS & ASSOCIATES

295 GEORGE STREET, SUITE 102 P.O. BOX 1234

SYDNEY, NOVA SCOTIA B1P 6J9

SUBMITTED BY:

AMEC EARTH & ENVIRONMENTAL LIMITED 55 TOWNSEND STREET SYDNEY, NOVA SCOTIA

B1P 5C6

TV21233 May 2003

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TABLE OF CONTENTS Page

1.0 INTRODUCTION ................................................................................................................ 1 2.0 PROGRAM DESCRIPTION ............................................................................................... 2

2.1 SUMMARY OF METHODS AND EQUIPMENT..................................................... 4 2.1.1 PM2.5............................................................................................................ 4 2.1.2 TSP and Metals .......................................................................................... 4 2.1.3 PM10 and Metals.......................................................................................... 4 2.1.4 PAHs ........................................................................................................... 4 2.1.5 VOCs........................................................................................................... 5

2.2 QA/QC SAMPLING................................................................................................. 5 2.3 FIELD OBSERVATIONS ........................................................................................ 5 2.4 WEATHER PARAMETER MEASUREMENTS ...................................................... 6

3.0 PROGRAM RESULTS...................................................................................................... 12 3.1 PM10, TSP AND METALS RESULTS................................................................... 12

3.1.1 PM2.5 Results............................................................................................. 13 3.2 PAH RESULTS ..................................................................................................... 14 3.3 VOC RESULTS..................................................................................................... 15 3.4 PROGRAM QA/QC............................................................................................... 16

3.4.1 VOCs......................................................................................................... 17 3.4.2 PAHs ......................................................................................................... 17 3.4.3 Metals........................................................................................................ 17

4.0 YEAR TO DATE AVERAGES, MAXIMUMS AND MINIMUMS ....................................... 18 5.0 CONCLUSIONS................................................................................................................ 22 6.0 REFERENCES ................................................................................................................. 23

LIST OF FIGURES

FIGURE 1 Sampling Locations................................................................................................. 3 FIGURE 2 February 8th Wind Rose Diagram for PIDC Weather Station................................. 8 FIGURE 3 February 20th Wind Rose Diagram for PIDC Weather Station............................... 9 FIGURE 4 February 8th Wind Rose Diagram for Coke Ovens Weather Station ................... 10 FIGURE 5 February 20th Wind Rose Diagram for Coke Ovens Weather Station ................. 11

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LIST OF TABLES Page TABLE 1 Summary of Sampling Locations and Parameters Analyzed................................. 2 TABLE 2 Summary of Metals Parameters Analyzed from Particulate Fractions .................. 4 TABLE 3 Summary of PAH Parameters Analyzed ................................................................ 5 TABLE 4 Summary of VOC Parameters Analyzed................................................................ 5 TABLE 5 Summary of Field Observations ............................................................................. 6 TABLE 6 Summary of Weather Information........................................................................... 7 TABLE 7 Summary of PM10, TSP and Metals Results February 8th Event ......................... 12 TABLE 8 Summary of PM10, TSP and Metals Results February 20th Event ....................... 13 TABLE 9 Summary of PM2.5 Results February 8th and 20th Events..................................... 13 TABLE 10 Summary of PAH Results February 8th Event ...................................................... 14 TABLE 11 Summary of PAH Results February 20th Event.................................................... 15 TABLE 12 Summary of VOC Results February 8th Event ..................................................... 15 TABLE 13 Summary of VOC Results February 20th Event ................................................... 16 TABLE 14 Field Duplicate Analyses by PSC and EC, February 20th .................................... 17 TABLE 15 Summary of Year to Date PM10/Metals Results ................................................... 18 TABLE 16 Summary of PM2.5 Results - December 2002 to February 2003 ......................... 19 TABLE 17 Summary of TSP/Metals Results – July 31st, 2002 to February 2003................. 19 TABLE 18 Summary of Year to Date PAH Results ............................................................... 20 TABLE 19 Summary of Year to Date VOC Results ............................................................... 21

LIST OF APPENDICES

APPENDIX A – Sampling Equipment Sketch and Procedure Description APPENDIX B – Data Validation Report APPENDIX C – Environment Canada VOC Duplicate Results

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1.0 INTRODUCTION This report provides a summary and interpretation of the Muggah Creek Remediation Project Ambient Air Monitoring Program results for the month of February 2003. In the fall of 2001, an expanded ambient air monitoring program (AAMP) was developed and implemented for the Sydney Muggah Creek Remediation Project. The AAMP was designed to monitor air quality within the Sydney airshed both prior to (background) and during the proposed remedial activities to be performed on the Sydney Tar Ponds and Coke Ovens site. The monitoring is being performed to determine whether there are any long-term and/or short-term effects on air quality from the proposed remedial activities, and also to assess impacts to the airshed from the Sydney Tar Ponds and Coke Ovens site during periods of inactivity. The program consists of sampling ambient air for total suspended particulate (TSP - 3 fixed locations), particulate matter less than 10 microns in diameter (PM10 - 3 fixed locations), metal parameters (4 fixed locations), as well as polyaromatic hydrocarbon (PAH) parameters and volatile organic compound (VOC) parameters at 6 fixed locations throughout Sydney. In addition, a mobile station is available to be used at various locations, depending on the location of remedial activities. Particulate matter less than 2.5 microns in diameter (PM2.5) was previously analyzed between the months of November 2001 and July 2002 on samples collected at 3 fixed locations, along with metals from the PM2.5 fraction. PM2.5 analysis was temporarily dropped from the AAMP because the laboratory detection limits were considered too high and did not meet the detection limit specified in the method for the analysis of PM2.5. AMEC has sourced a laboratory with equipment that can achieve the applied method detection limit. As a result, the PM2.5 analysis at 3 fixed locations was reinstated in December 2002 to the program’s sampling/analytical scope. Only a few metals were being detected from the PM2.5 and, as a result, the metals analysis was permanently dropped from the AAMP. This report summarizes air monitoring results for two sampling events, performed on February 8th and 20th.

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2.0 PROGRAM DESCRIPTION The AAMP consists of sampling at six fixed locations throughout Sydney. Table 1 provides a summary of the fixed sampling locations and parameters to be sampled at each location.

TABLE 1

Summary of Sampling Locations and Parameters Analyzed

Parameter Victoria

Road STATION 1

Frederick Street

STATION 2

Henry Street

STATION 3

Kings Road

STATION 4

Intercolonial Street

STATION 5

DesBarres Street

STATION 6 PM2.5 h h h PM10 h h h Metals in PM10 fraction h h h

TSP h h h Metals in TSP fraction h h h

PAH h h h h h h VOC h h h h h h

Refer to Figure 1 for the sampling locations. The sampling frequency for the program follows a 6-day National Air Pollution Surveillance (NAPS) schedule during periods when activity is occurring at the Tar Ponds and/or Coke Ovens site. The sampling during periods of non-activity is performed on a 12-day schedule falling on NAPS days. The sampling duration for each event is 24-hours (midnight to midnight). Sampling falling on NAPS days was performed on February 8th and 20th. Weather information for the program during the month of February was obtained from the two project weather stations, one located at the former Public Information Display Centre (PIDC) site, off of Terminal Road, and the other at the southeast end of the Coke Ovens site. Additional meteorological data (humidity, precipitation, barometric pressure and fog) was acquired from the Environment Canada weather station located at the Sydney Airport.

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2.1 SUMMARY OF METHODS AND EQUIPMENT The field program consisted of sampling for PM2.5 using low volume sampling equipment, PM10, PAHs, TSP and metals, using high volume sampling equipment, and VOCs using stainless steel evacuated canisters. The following provides a summary of methods for sampling, parameters analyzed and equipment employed. Refer to Appendix “A” for a sketch of the equipment and a description of sampling procedures. 2.1.1 PM2.5 Sampling for PM2.5 was conducted in accordance with the United States Environmental Protection Agency (USEPA) Reference Method for the Determination of Fine Particulate Matter as PM2.5 in the Atmosphere (40 CFR, Subchapter C, Part 50, Appendix L). Sampling was performed with the BGI PQ-200 PM2.5 sampling system. The media used to capture PM2.5 were 47 mm polytetrafluoroethylene (PTFE) teflon filters. Analysis was performed at Chester LabNet in Tigard, Oregon, USA. 2.1.2 TSP and Metals The sampling protocol for TSP was in accordance with the Environment Canada Method for the Measurement of Suspended Particulate in the Atmosphere (Environment Canada, 1973). All sampling was performed with Tisch High Volume samplers. Calibration of each sampler was completed using orifice resistance plates and a water manometer. Initial and final flow checks were performed on each instrument for the 24-hour sampling period. The media used to capture TSP and metals were quartz filters. Analyses were performed at the Environmental Services Laboratory (ESL) in Sydney. Refer to Table 2 for a list of metals parameters analyzed from the TSP fraction.

TABLE 2 Summary of Metals Parameters Analyzed from Particulate Fractions

Aluminum Boron Calcium Lithium Silver Uranium Magnesium Selenium Antimony Cadmium Copper Manganese Sodium Vanadium Potassium Mercury (1) Barium Chromium Iron Molybdenum Thallium Zinc Sulfur Beryllium Cobalt Lead Nickel Tin Strontium Arsenic

Note: (1) Mercury is analyzed as only the particulate fraction.

2.1.3 PM10 and Metals Sampling for PM10 was performed in accordance with the USEPA Reference Method for the Determination of Particulate Matter as PM10 in the Atmosphere (40 CFR, Part 50, Appendix M). All sampling was performed with either Graesby Anderson or Tisch High Volume samplers. Initial and final flow checks were performed during the 24-hour sampling period. The media used to capture PM10 and metals were quartz filters. ESL performed the analyses. Refer to Table 2 for a list of metals parameters analyzed from the PM10 fraction. 2.1.4 PAHs PAH compounds were sampled in accordance with the USEPA TO13A Method. All sampling was performed with either Graesby Anderson or Tisch High Volume samplers. Initial and final flow checks were performed on each sampler during the 24-hour sampling period. The media used to capture PAH compounds were glass-fibre filters with a polyurethane foam (PUF)

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sorbent backup. ESL performed sample media preparation and analyses. Refer to Table 3 for a list of PAH parameters analyzed.

TABLE 3 Summary of PAH Parameters Analyzed

Naphthalene Fluorene Fluoranthene Chrysene Indeno(1,2,3-cd)pyrene Acenaphthylene Phenanthrene Pyrene Benzo Fluoranthene Dibenz(a,h)anthracene Acenaphthene Anthracene Benzo(a)anthracene Benzo(a)pyrene Benzo(g,h,i)perylene

2.1.5 VOCs Sampling for VOCs was performed in accordance with the USEPA TO14A Method. An evacuated stainless steel canister was used to collect a sub-atmospheric (pressure) sample. A flow restrictive device (cantroller) was employed to acquire the samples over a 24-hour period. The evacuated canisters were transported to the Philip Service Corporation (PSC) analytical laboratory in Burlington, Ontario for analyses. Refer to Table 4 for the list of VOCs analyzed.

TABLE 4 Summary of VOC Parameters Analyzed

Dichlorodifluoromethane Chloroform 1,1,1-Trichloroethane Carbon tetrachloride 1,3-Dichlorobenzene

Chloromethane 1,1-Dichloroethene 1,1,2-Trichloroethane Ethylene dibromide 1,4-Dichlorobenzene

Halocarbon 114 cis-1,2-Dichloroethene Toluene Ethylbenzene 1,2-Dichlorobenzene

Vinyl chloride 1,1-Dichloroethane Benzene m&p-Xylene 1,2,4-Trichlorobenzene

Chloroethane 1,2-Dichloropropane cis-1,3-Dichloropropene o-Xylene Hexachlorobutadiene

1,2-Dichloroethane Dichloromethane trans-1,3-Dichloropropene 1,3,5-Trimethylbenzene Chlorobenzene

Bromomethane 1,1,2,2-Tetrachloroethane Trichloroethene 1,2,4-Trimethylbenzene

Trichlorofluoromethane Tetrachloroethene Halocarbon 113 2.2 QA/QC SAMPLING The February 8th QA/QC sampling consisted of obtaining field blanks for PAHs at the Victoria Road location, PM10 and metals at the Frederick Street location, TSP and metals at the Henry Street location and PM2.5 at the Kings Road location. All QA/QC sample analyses was performed at PSC. The February 20th QA/QC sampling consisted of obtaining duplicate samples for PAHs at the Frederick Street location, PM10 and metals at the Victoria Road location and VOCs at the Intercolonial Street location. The duplicate sample set for VOCs was forwarded to Environment Canada’s laboratory for analysis after PSC analyzed the samples. 2.3 FIELD OBSERVATIONS The monitoring program was performed from midnight to midnight on February 8th and 20th. Table 5 provides a summary of field observations for each sampling day.

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TABLE 5 Summary of Field Observations

Sampling Event Date Observations February 8th • Snowfall on February 8th resulted in snow removal activities occurring throughout the day of sampling.

• No activity visible on the Coke Ovens site during the event (Saturday). February 20th • Chimney smoke-like odour detected by olfaction near the Henry Street location during the event check on

February 20th at approximately 12:15 pm. • Truck traffic visible on Frederick Street and the new Port Access Road during the event check on

February 20th at approximately 12:30 pm. • Loaders working on slag piles north of the DesBarres Street location during the event check at

approximately 12:00 pm. • Crane driving piles into the Government Wharf for a building expansion during the event check at

approximately 12:00 pm. • Train shunting back and forth near the DesBarres Street location during the event check on February 20th

at approximately 12:00 pm. • No visible activity on the Coke Ovens site during the entire event.

2.4 WEATHER PARAMETER MEASUREMENTS Weather information for the wind speed, wind direction and temperature parameters were obtained from the project weather station located at the former PIDC site and from the project weather station situated at the Coke Ovens site. The PIDC project weather station is located south of the South Tar Pond, off of Terminal Road, and is approximately 900 metres from the southwest corner of the Coke Ovens site (Figure 1). The Coke Ovens project weather station is situated at the southeast perimeter of the Coke Ovens site approximately 625 metres to the east of the Victoria Road sampling location (Figure 1). Relative humidity, precipitation, barometric pressure, fog and snow cover were obtained from the Sydney Airport Environment Canada weather station. All measurements were recorded on an hourly basis. Table 6 provides a summary of weather measurements for each 24-hour sampling day for February 2003.

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TABLE 6 Summary of Weather Information

% Frequency February 8th

% Frequency February 20th

Wind Direction During Monitoring Period PIDC Project Weather Station

Coke Ovens Project Weather Station

PIDC Project Weather Station

Coke Ovens Project Weather Station

N 8.3 4.2 -- -- NNE 4.2 12.5 -- -- NE 8.3 12.5 -- -- ENE 12.5 8.3 -- -- E 4.2 -- -- -- ESE -- -- -- -- SE -- -- -- -- SSE -- -- -- -- S 4.2 4.2 37.5 25.0 SSW 4.2 -- 33.3 33.3 SW 8.3 4.2 8.3 16.7 WSW 8.3 16.6 -- 8.3 W 12.5 8.3 16.7 12.5 WNW 12.5 12.5 4.2 4.2 NW 12.5 4.2 -- -- NNW -- 12.5 -- -- Calm -- -- -- -- Average Wind speed (km/hr) [m/s] 20.0 [5.6] 36.7 [10.2] 15.8 [4.4] 29.1 [8.1] Average Temperature (ºC) -5.6 -5.5 -2.0 -1.7 Minimum Temperature (ºC) -11.4 -11.6 -4.9 -4.7 Maximum Temperature (ºC) -1.7 -1.7 1.7 2.7

ENVIRONMENT CANADA MONTHLY DATA Relative Humidity (%) 75 73 Total Precipitation (mm) (rain (mm) /snow (cm)) (1) 7.8 [0.0 / 7.8] 3.6 [0.0 / 3.6] Barometric Pressure (kPa) 99.44 100.62 Fog NO NO Snow Cover YES YES Notes: (1) Rain is reported in mm, snow in cm.

Figures 2 to 5 provide graphical presentations of wind direction and speed in the form of wind roses inset on a plan view of the sampling locations for each sampling day. The wind roses provide information on wind frequency, direction and speed for each sampling day. The length of each bar for a direction indicates the percent of time the wind blows from that direction. The wind direction is defined as that from which the wind is blowing (i.e., a north wind comes from the north). Each hatch pattern within the wind rose bars represents the percentage of time for a velocity. A legend is included on each wind rose for interpretation. Winds were predominately from the ENE/W/WNW/NW directions on February 8th and S/SSW on February 20th at the PIDC project weather station. Winds were prevailing from the WSW on February 8th and SSW on February 20th at the Coke Ovens project weather station. The winds at the PIDC project weather station location were strongest on February 8th with an average wind speed of 20.0 km/hr and weakest on February 20th with an average wind speed of 15.8 km/hr. The winds at the Coke Ovens project weather station location were strongest on February 8th with an average wind speed of 36.7 km/hr and weakest on February 20th with an average wind speed of 29.1 km/hr. We note that the wind speed readings at the Coke Ovens project weather station were higher by approximately 84% than the wind speed readings at the PIDC project weather station. Comparisons with wind speeds at the Sydney Airport Environment Canada weather station were made for the month of November 2002. The Airport data is more comparable to the PIDC weather data than to the Coke Ovens project weather data. Environment Canada is currently examining the equipment at the PIDC and Coke Ovens project weather stations to determine whether the variances are equipment related or not.

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3.0 PROGRAM RESULTS The following section provides a summary of PM10, TSP, metals, PM2.5, PAH and VOC results for the month of February. The tables in this section summarize only those values that were detected. Refer to Appendix “B” for a complete set of results contained in the Data Validation Report. A review of available Nova Scotia standards and guidelines indicate that Nova Scotia only provides an ambient air quality objective for one of the parameters, TSP. However, the province of Ontario does provide ambient air quality criteria (AAQC) for many of the program PAH, VOC and metal parameters and these have been included in the tables for this section. Currently, Nova Scotia does not have an objective for PM10. Discussions with Environment Canada have determined that the use of criteria developed in other jurisdictions is acceptable. For the Sydney AAMP, a 24-hour criterion of 50 µg/m3 for PM10 has been applied, which is the criterion being used in Ontario and British Columbia. The monitoring locations at the perimeter of the Coke Ovens site are the exception, where a 24-hour criterion of 25 µg/m3 for PM10 has been applied during periods of activity at the site, as developed in the Interim Separation Zone criteria study (AGRA, 2000). Criteria for metals, PAHs and VOCs were also developed in the Interim Separation Zone study, to be applied around the perimeter of the Coke Ovens site during periods of activity at the Coke Ovens site. 3.1 PM10, TSP AND METALS RESULTS Tables 7 and 8 provide a summary of PM10, TSP and metals results for the February 8th and 20th sampling events, respectively.

TABLE 7 Summary of PM10, TSP and Metals Results February 8th Event(1)

Parameter

Victoria Road PM10

Results (µµµµg/m3)

Frederick Street PM10

Results (µµµµg/m3)

Frederick Street PM10

Field Blank Results

(mg/filter)

DesBarres Street PM10

Results (µµµµg/m3)

24-hour Guidelines

(µµµµg/m3)

Victoria Road TSP

Results (µµµµg/m3)

Frederick Street TSP

Results (µµµµg/m3)

Henry Street TSP

Results (µµµµg/m3)

Henry Street TSP

Field BlankResults

(mg/filter)

24-Hour Criteria(3) (µµµµg/m3)

PM10 7.9 6.4 1.1 8.4 50(3) NA(2) NA NA NA NA TSP NA NA NA NA NA 13.5 12.0 14.1 1.1 120(4) Copper <0.01 U 0.01 <0.02 U <0.01 U na(5) 0.03 0.02 0.03 <0.02 U 50 Lead <0.001 U 0.002 <0.002 U <0.001 U na 0.002 <0.001 U 0.003 <0.002 U 5 Arsenic <0.001 U 0.002 <0.002 U 0.002 na <0.001 U <0.001 U 0.006 <0.002 U 0.3 Notes : (1) Not detected values are reported at detection limit and are shown with a < symbol.

(2) NA denotes not applicable. (3) Ontario MOE 24-hour Ambient Air Quality Criteria. (4) Nova Scotia Ambient Air Quality Objective for a 24-hour averaging period. (5) na denotes not available. U = Non-detected at the stated limit.

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TABLE 8 Summary of PM10, TSP and Metals Results February 20th Event(1)

Parameter

Victoria Road PM10

Results (µµµµg/m3)

Victoria Road PM10

Duplicate Results (µµµµg/m3)

Frederick Street PM10

Results (µµµµg/m3)

DesBarres Street PM10

Results (µµµµg/m3)

24-hour Guidelines

(µµµµg/m3)

Victoria Road TSP

Results (µµµµg/m3)

Frederick Street TSP

Results (µµµµg/m3)

Henry Street TSP

Results (µµµµg/m3)

24-Hour Criteria(3) (µµµµg/m3)

PM10 0.7 1.6 3.2 2.0 50(3) NA(2) NA NA NA TSP NA NA NA NA NA 2.1 R 9.2 2.5 BL 120(4) Copper 0.04 0.12 0.03 0.02 na(5) 0.37 0.26 0.18 50 Iron <0.1 U <0.1 U 0.1 <0.1 U na 0.1 0.16 0.05 4 Lead 0.003 0.003 0.004 0.006 na 0.006 0.007 0.012 5 Sodium 0.4 <0.3 U <0.4 U <0.3 U na 1.3 0.6 0.6 na Tin <0.01 U <0.01 U <0.01 U 0.01 na <0.01 U <0.01 U <0.01 U 10 Vanadium <0.001 U 0.001 0.002 0.001 na 0.001 0.003 0.003 2 Zinc <0.1 U <0.1 U <0.1 U <0.1 U na 0.1 <0.1 U <0.1 U 120 Arsenic <0.001 U 0.001 0.002 0.010 na 0.001 0.003 0.011 0.3 Notes: (1) Not detected values are reported at detection limit and are shown with a < symbol.

(2) NA denotes not applicable. (3) Ontario MOE 24-hour Ambient Air Quality Criteria. (4) Nova Scotia Ambient Air Quality Objective for a 24-hour averaging period. (5) na denotes not available. U = Non-detected at the stated limit. R = Rejected, see text for explanation. BL = Biased low, see text for explanation.

Nova Scotia provides a 24-hour objective of 120 µg/m3 for the TSP parameter and the Ontario Ministry of Environment (MOE) provides a 24-hour AAQC of 50 µg/m3 for the PM10 parameter. A comparison of the TSP results with the Nova Scotia objective and the PM10 results with MOE AAQC indicates there were no exceedances for these parameters during the month of February. It is noted that the total mass for the metals reported exceeded the TSP gravimetric result at the Victoria Road location. Hence, the TSP result was rejected. A comparison of metals results for PM10 to regulatory criteria could not be performed since there are currently no regulations or guidelines for Nova Scotia, the rest of Canada nor the United States for metals that are sampled from the PM10 fraction. There were no exceedances to available metals AAQC for the Victoria Road, Frederick Street and Henry Street TSP samples. 3.1.1 PM2.5 Results Table 9 provides a summary of PM2.5 results for the February 8th and 20th events.

TABLE 9 Summary of PM2.5 Results February 8th and 20th Events

February 8th February 20th

Parameter Henry Street PM2.5

Results (µµµµg/m3)

Kings Road PM2.5

Results (µµµµg/m3)

Kings Road PM2.5

Field Blank Results

(mg/filter)

Intercolonial Street PM2.5

Results (µµµµg/m3)

Henry Street PM2.5

Results (µµµµg/m3)

Kings Road PM2.5

Results (µµµµg/m3)

Intercolonial Street PM2.5

Results (µµµµg/m3)

24-hour Standard (µµµµg/m3)

PM2.5 11.55 4.87 0.008 4.91 9.04 7.16 7.95 30(1)

Notes: (1) CCME 24-hour Canada Wide Standard.

The Canadian Council of the Ministers of the Environment (CCME) provides a Canada wide Standard (CWS) of 30 µg/m3 for the PM2.5 parameter. A comparison of the PM2.5 results with the CWS indicates there were no exceedances during the month of February. It is also noted that on February 20th, the Henry Street PM2.5 result is higher than the TSP result for the same location. The TSP result is considered anomalously low, since PM2.5 is a part of

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TSP, and therefore, should never be lower than PM2.5. The reason for this anomalous result is unknown. Probable explanations include a loss of a portion of filter in the field or laboratory error. Since the total mass for metals did not exceed the TSP result, the sample was not rejected but considered biased low. 3.2 PAH RESULTS Tables 10 and 11 provide a summary of PAH results for the February 8th and 20th sampling events, respectively.

TABLE 10 Summary of PAH Results February 8th Event(1)

Parameter Victoria Road

Result (ng/m3)

Frederick Street Result (ng/m3)

Victoria Road Field Blank

Result (µg/PUF)

Henry StreetResult (ng/m3)

Kings Road Result (ng/m3)

Intercolonial Street Result (ng/m3)

DesBarres Street Result (ng/m3)

Ontario Ambient

Air Quality 24-hour Criteria (ng/m3)

Naphthalene 3.6 JM 2.5 JM 0.09 JM 10.6 JM 0.94 UB 3.2 JM 3.7 JM 22500 Acenaphthylene 1.15 2.25 <0.05 U 7.4 0.21 0.96 0.92 na (2) Acenaphthene 0.56 0.72 <0.05 U 1.67 0.13 0.79 0.69 na Fluorene 1.98 2.37 <0.05 U 3.7 0.75 1.90 1.56 na Phenanthrene 4.8 6.2 <0.05 U 13.2 2.01 5.2 5.0 na Anthracene 0.48 0.70 <0.05 U 2.38 0.13 0.47 0.42 na Fluoranthene 0.94 2.15 <0.05 U 4.5 0.40 0.94 1.06 na Pyrene 0.84 1.82 <0.05 U 4.0 0.32 0.74 0.84 na Benzo(a)anthracene 0.18 0.35 <0.1 U 1.22 <0.13 U 0.20 0.34 na Chrysene 0.28 0.45 <0.05 U 1.22 <0.13 U 0.27 0.37 na Benzo Fluoranthene 0.46 0.80 <0.05 U 2.09 <0.3 U 0.47 0.58 na Benzo(a)pyrene 0.15 0.27 <0.05 U 0.87 <0.13 U 0.15 0.24 1.1 Indeno(1,2,3-cd)pyrene 0.25 0.40 <0.05 U 0.93 <0.13 U 0.25 0.26 na Dibenz(a,h)anthracene <0.13 U <0.12 U <0.05 U 5.4 <0.13 U <0.12 U <0.13 U na Benzo(g,h,i)perylene 0.28 0.30 <0.05 U 0.74 <0.13 U 0.22 0.21 na Total PAH (3) 16.0 21.3 NA(4) 54.7 5.4 15.8 16.3 na Notes: (1) not detected values are reported at detection limit and are shown with a < symbol. (2) na denotes not available. (3) Total PAH is the sum of all reported values, including PAHs with values reported as non-detect, using values at half the detection limit. (4) NA denotes not applicable. U = Non-detected at the stated limit. UB = Non-detected with elevated reporting limit as a result of method and/or field blank contamination. JM = Estimated value; recovery from matrix spike indicates potential low bias.

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TABLE 11 Summary of PAH Results February 20th Event(1)

Parameter Victoria Road

Result (ng/m3)

Frederick Street Result (ng/m3)

Frederick Street

Duplicate Result (ng/m3)

Henry StreetResult (ng/m3)

Kings Road Result (ng/m3)

Intercolonial Street Result (ng/m3)

DesBarres Street Result (ng/m3)

Ontario Ambient

Air Quality 24-hour Criteria (ng/m3)

Naphthalene 0.87 UB 0.48 UB 0.42 UB 2.9 0.76 UB 0.94 UB 0.95 UB 22500 Acenaphthylene 0.87 0.58 0.49 6.3 0.32 0.81 2.9 na (2) Acenaphthene 0.41 0.78 0.84 0.60 0.16 0.42 0.66 na Fluorene 2.20 2.23 2.02 5.5 0.84 2.07 3.4 na Phenanthrene 5.4 4.5 3.7 19.4 2.7 4.4 11.6 na Anthracene 0.36 0.30 0.29 3.4 0.16 0.32 1.24 na Fluoranthene 0.82 0.50 0.61 6.6 0.49 0.69 3.7 na Pyrene 0.74 0.65 0.54 7.1 0.35 0.64 3.2 na Benzo(a)anthracene <0.13 U <0.13 U <0.12 U 1.05 <0.14 U <0.12 U 0.69 na Chrysene 0.18 0.20 0.17 1.97 <0.14 U 0.15 0.85 na Benzo Fluoranthene 0.28 0.28 0.2 2.6 <0.3 U <0.2 U 1.14 na Benzo(a)pyrene <0.13 U <0.13 U <0.12 U 1.00 <0.14 U <0.12 U 0.48 1.1 Indeno(1,2,3-cd)pyrene <0.13 U <0.13 U <0.12 U 1.00 <0.14 U <0.12 U 0.42 na Dibenz(a,h)anthracene <0.13 U <0.13 U <0.12 U 0.16 <0.14 U <0.12 U <0.13 U na Benzo(g,h,i)perylene 0.13 0.13 0.12 1.08 <0.14 U <0.12 U 0.29 na Total PAH (3) 12.4 10.9 9.6 60.7 6.4 10.8 31.6 na Notes: (1) not detected values are reported at detection limit and are shown with a < symbol. (2) na denotes not available. (3) Total PAH is the sum of all reported values, including PAHs with values reported as non-detect, using values at half the detection limit. U = Non-detected at the stated reporting limit. UB = Non-detected with elevated reporting limit as a result of method and/or field blank contamination.

All results for naphthalene and benzo(a)pyrene were below the Ontario Ministry of the Environment 24-hour criteria. It is noted that the total PAH results are higher at the Henry Street location compared to the rest of the locations for both sampling events. Smoke-like odours were noted during the February 20th event. It is likely that this location is being impacted from emissions originating from the chimneys of residential units located in the vicinity of the sampling location. The same is likely for February 8th when a higher PM2.5 value was reported for Henry Street than other locations. 3.3 VOC RESULTS Tables 12 and 13 provide a summary of VOC results for the February 8th and 20th sampling events. A VOC duplicate sample was collected on February 20th at the Intercolonial Street location and this duplicate set of samples was forwarded to Environment Canada (EC) for further analysis. A copy of the EC results is contained in Appendix “C”.

TABLE 12 Summary of VOC Results February 8th Event(1)

Parameter MDL (µµµµg/m3)

Victoria Road

Results (µµµµg/m3)

Frederick Street

Results (µµµµg/m3)

Henry Street

Results (µµµµg/m3)

Kings Road

Results (µµµµg/m3)

Intercolonial Street

Results (µµµµg/m3)

DesBarres Street

Results (µµµµg/m3)

Ontario Ambient

Air Quality 24-hour Criteria (µµµµg/m3)

Dichlorodifluoromethane 0.71 0.85 JC 0.78 JC 0.74 JC 0.81 JC 0.71 JC <1.49 U 500,000 Dichloromethane 0.76 <2.50 UB <0.76 U <1.46 UB <0.76 U <0.76 U <2.64 UB 1,765 1,1,1-Trichloroethane 0.76 <0.76 U <0.76 U <0.76 U <0.76 U 0.82 JC <1.58 U 115,000 Toluene 0.49 <0.49 U <0.49 U 0.49 JC <0.49 U <0.49 U <1.02 U 2,000 Benzene 0.58 0.70 JC <0.58 U 0.64 JC <0.58 U 0.89 JC 3.5 JC na(2) Notes: (1) not detected values are reported at detection limit and are shown with a < symbol (2) na denotes not available MDL denotes method detection limits U = Non-detected at the stated limit. UB = Non-detected with elevated reporting limit as a result of background laboratory and/or canister contamination. JC = Estimated value, measured at less than ½ the low calibration standard.

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TABLE 13 Summary of VOC Results February 20th Event(1)

Parameter MDL (µµµµg/m3)

Victoria Road

Results (µµµµg/m3)

Frederick Street

Results (µµµµg/m3)

Henry Street

Results (µµµµg/m3)

Kings Road

Results (µµµµg/m3)

IntercolonialStreet

Results (µµµµg/m3)

Intercolonial Street

Duplicate Results (µµµµg/m3)

DesBarres Street

Results (µµµµg/m3)

Ontario Ambient

Air Quality24-hour Criteria (µµµµg/m3)

Dichlorodifluoromethane 0.71 <0.71 U <0.71 U <1.20 U 0.74 JC <1.13 U 1.41 JC <0.71 U 500,000 Dichloromethane 0.76 <0.76 U <0.76 U <2.95 UB <1.84 UB <3.27 UB <4.2 UB <1.63 UB 1,765 Halocarbon 113 1.15 1.30 JC <1.15 U <1.99 U <1.15 U <1.84 U <2.07 U <1.15 U 80,000 1,1,1-Trichloroethane 0.76 <0.76 U <0.76 U <1.31 U <0.76 U 1.47 JC <1.36 U 0.87 JC 115,000 Toluene 0.49 0.53 JC <0.49 U 2.26 JC <0.49 U 1.13 JC 1.70 JC <0.49 U 2,000 Benzene 0.58 0.89 JC <0.58 U 1.63 JC 0.83 JC 1.12 JC <1.02 U 0.89 JC na(2) Notes: (1) not detected values are reported at detection limit and are shown with a < symbol (2) na denotes not available MDL denotes method detection limits U = Non-detected at the stated limit. UB = Non-detected with elevated reporting limit as a result of background laboratory and/or canister contamination. JC = Estimated value, measured at less than ½ the low calibration standard.

Currently, there are no ambient air regulations or guidelines for Nova Scotia covering the VOC parameters. The Province of Ontario provides guidelines for most of the parameters identified in Tables 12 and 13 and these guidelines have been included for comparison with the measured concentrations. A review of results compared to the Ontario AAQC indicates that all results are below the guideline values. 3.4 PROGRAM QA/QC Refer to Appendix “B” for a copy of the February Data Validation Report. The data generated for this program are supported by quality assurance/quality control measures and can be relied upon for program purposes. Accuracy, precision and completeness met or exceeded program objectives for most analyses. The uncertainties in measurements that exist in the data set for VOCs and metals are primarily reflections of the low levels of compounds present in the ambient air. VOCs and metals, when detected, were essentially just above the laboratory method detection limit, and well below the referenced guidelines. With very limited exceptions, the data, taking into consideration the qualifications applied from validation, may be used with confidence for air quality characterization. The text for the February Data Validation Report details the reasons for all qualifications to data. Quantitative results may be qualified as estimated for a variety of reasons including: measurements below the demonstrated linear range of the instrument; high or low recoveries of surrogate compounds or matrix spike compounds (samples to which target compounds have been added); canister flow uncertainties; and changes in the pressure of a canister between the end of the sampling event and receipt at the lab. The bottom line is that the identification is reliable but the measured concentration has a degree of uncertainty to it. When possible, the text provided limits to this uncertainty; for example, if the surrogate recovery is low, the sample results are likely low to a comparable degree and low surrogate recovery probably indicates that the measured result represents only a portion of the actual air concentration. In many cases, however, it is not possible to establish clear limits for the uncertainty. The sample specific reasons for data qualification are summarized in the footnotes of the tables in Sections 3.1 to 3.3 and detailed in Appendix “B”. The following provides a summary of the data validation findings for the VOC, PAH and metals parameters.

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3.4.1 VOCs Most volatiles detected were at concentrations less than one half the low calibration standard and are qualified as estimated (JC) since the linearity of the instrument response cannot be assumed. Results for dichloromethane (methylene chloride) have been qualified as non-detected with elevated reporting limits as a result of laboratory background (UB). Table 14 presents data for the replicate analyses of field duplicate samples by PSC and EC collected on February 20th at the Intercolonial Street location. All detected analytes present were below ½ the low calibration standard at PSC and are qualified as estimated. Concentrations reported by EC were consistently higher by a factor of approximately two. The EC analyses are conducted using a different technique that provides lower detection limits for target analytes; differences in results between the two laboratories near or at the PSC reporting limits are within method expectations.

TABLE 14 Field Duplicate Analyses by PSC and EC, February 20th

PSC EC

Intercolonial Street

Intercolonial Street Field Duplicate

Intercolonial Street

Intercolonial Street Field Duplicate

Component

ppbv ppbv

RPD PSC

ppbv ppbv

RPD EC

RPD, PSC/EC

Freon 12 (Dichlorodifluoromethane) <0.32U 0.40JC NA(1) 0.717 0.833 15% NA 100%Chloromethane <0.46U <0.52U NA 0.561 0.544 3% NA NA Dichloromethane <0.94UB <1.2UB NA 2.093 2.568 20% NA NA 1,1,1-Trichloroethane 0.27JC <0.25U NA 0.596 0.383 43% 75% NA Benzene 0.35JC <0.32U NA 0.618 0.416 39% 55% NA Trichloroethylene <0.27U <0.31U NA 0.379 0.300 23% NA NA Toluene 0.30JC 0.45JC 40% 0.891 1.199 30% 99% 85%

Notes: (1) NA denotes not applicable when one result below the method detection limit. JC = Estimated value; measured at less than 1/2 the low calibration standard. U = Non-detected at the stated limit. UB = Non-detected with elevated reporting limit as a result of background laboratory and/or canister contamination RPD = relative percent difference.

3.4.2 PAHs Results for naphthalene from the February 8th sampling event are qualified as estimated with potential low bias as a result of recoveries below 60% from the matrix spike samples. Naphthalene was also present in the February 8th field blank, but at a trace level that affected only the Kings Road sample result. Naphthalene was also present in the method blank for the February 20th; therefore results for all samples in this set except the Henry Street sample were qualified as non-detected with elevated reporting limits. 3.4.3 Metals No metals were detected in the method blanks or field blanks for the PM10 and TSP samples. Gravimetric results for TSP for the Victoria Road sample on February 20th were rejected since the mass of individual metals reported exceeded the reported TSP. The TSP result for Henry Street is considered biased low (BL) because the PM2.5 result is higher than the TSP result. The TSP result could not be rejected because the mass of individual metals does not exceed the TSP value.

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4.0 YEAR TO DATE AVERAGES, MAXIMUMS AND MINIMUMS This section provides a summary, including running averages, maximum and minimums, of the last 12 months of program data (March 2002 to February 2003). Refer to Tables 15, 18 and 19 for a summary of the PM10/metals, PAH and VOC for the March 2002 to February 2003 time period, respectively. Table 16 presents the summary for the PM2.5, which includes sampling performed for the time period of December 2002 to February 2003. TSP and metals results summarized for the time period of July 31st, 2002 to the end of February 2003 are contained in Table 17. It should be noted that averages were not calculated for sample sets where all results were reported as below the method detection limit. For sample sets where at least one value in the sample set is reported as above the method detection limit, the values below the method detection limit are used in the calculation of averages by inputting values at half the reported method detection limit. In some instances there is an average value reported when the maximum is reported as below the method detection limit. The reason is that there was at least one value reported in the data set as being detected and the value(s) happens to be below the maximum reported detection limit on the tables.

TABLE 15 Summary of Year to Date PM10/Metals Results(1)

Victoria Road Frederick Street DesBarres Street Parameter Average

(µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3) PM10 10.4 0.7 27.1 21.7 1.9 169.0 12.7 1.1 36.1 Aluminum 0.1 <0.1 0.5 0.3 <0.1 3.2 0.1 <0.1 0.4 Antimony 0.002 <0.001 0.054 0.001 <0.001 0.002 -- <0.001 <0.001 Barium 0.01 <0.01 0.03 0.01 <0.01 0.03 0.01 <0.01 0.03 Beryllium --(2) <0.001 <0.001 -- <0.001 <0.001 -- <0.001 <0.001 Boron -- <0.1 <0.2 -- <0.1 <0.1 -- <0.1 <0.1 Cadmium -- <0.001 <0.001 -- <0.001 <0.001 -- <0.001 <0.001 Chromium 0.001 <0.001 0.003 0.001(3) <0.001 <0.005 0.001(3) <0.001 <0.004 Cobalt 0.001 <0.001 0.004 0.001(3) <0.001 <0.005 0.001 <0.001 0.002 Calcium 0.3 <0.4 1.2 0.3 <0.4 1.8 0.4 <0.4 4.7 Copper 0.05 <0.01 0.23 0.04 <0.01 0.12 0.04 <0.01 0.23 Iron 0.1 <0.1 0.6 0.5 <0.1 7.7 0.1 <0.1 1.4 Lead 0.006 <0.001 0.104 0.003 <0.001 0.027 0.003 <0.001 0.014 Lithium 0.001(3) <0.001 <0.034 0.001(3) <0.001 <0.005 -- <0.001 <0.036 Manganese 0.01 <0.01 0.02 0.02 <0.01 0.25 0.01 <0.01 0.07 Molybdenum -- <0.01 <0.01 -- <0.01 <0.01 -- <0.01 <0.01 Nickel 0.003(3) <0.003 <0.076 0.003(3) <0.003 <0.028 0.003(3) <0.003 <0.079 Silver -- <0.001 <0.001 0.001 <0.001 0.002 -- <0.001 <0.001 Sodium 0.5 <0.3 3.6 0.5 <0.4 3.9 0.5(3) <0.3 <4.0 Thallium -- <0.001 <0.001 -- <0.001 <0.001 -- <0.001 <0.001 Tin -- <0.01 <0.01 -- <0.01 <0.01 0.01 <0.01 0.01 Uranium -- <0.0001 <0.001 -- <0.0001 <0.001 -- <0.0001 <0.001 Vanadium 0.001 <0.001 0.005 0.002 <0.001 0.010 0.002 <0.001 0.023 Zinc -- <0.1 <0.1 0.03(3) <0.1 <0.1 -- <0.1 <0.1 Strontium 0.002 <0.003 0.004 0.002 <0.003 0.004 0.002 <0.003 0.009 Magnesium 0.1 <0.1 0.6 0.2 <0.1 2.1 0.1 <0.1 0.4 Potassium -- <0.3 <0.6 0.2(3) <0.3 <0.6 0.2 <0.3 0.5 Sulphur -- <2.0 <2.6 -- <1.9 <2.5 1.2 <2.0 2.6 Arsenic 0.001 <0.001 0.003 0.001 <0.001 0.008 0.002 <0.001 0.012 Selenium 0.001 <0.001 0.006 0.001 <0.001 0.006 0.001 <0.001 0.004 Mercury -- <0.0001 <0.0001 -- <0.0001 <0.0001 -- <0.0001 <0.0001 Notes: (1) not detected values are reported at detection limit and are shown with a < symbol. (2) -- not applicable. (3) An average value has been reported because there was at least one detected value below the maximum method detection limit during the reporting period.

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TABLE 16 Summary of PM2.5 Results - December 2002 to February 2003(1)

Henry Street Kings Road Intercolonial Street

Parameter Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average(µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3) PM2.5 7.6 3.42 11.5 5.7 4.29 7.2 5.6 3.12 8.0 Notes: (1) Average, minimum and maximum are calculated using results from December 2002 to February 2003.

TABLE 17

Summary of TSP/Metals Results – July 31st, 2002 to February 2003(1)

Victoria Road Frederick Street Henry Street Parameter Average

(µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3) TSP 25.7 5.6 56.6 27.8 3.6 115.8 21.5 2.5 54.3 Aluminum 0.1 <0.1 0.4 0.2 <0.1 0.7 0.1 <0.1 0.7 Antimony --(2) <0.001 <0.001 -- <0.001 <0.001 -- <0.001 <0.001 Barium 0.01 <0.01 0.03 0.01 <0.01 0.04 0.01 <0.01 0.03 Beryllium -- <0.001 <0.001 -- <0.001 <0.001 -- <0.001 <0.001 Boron -- <0.1 <0.1 -- <0.05 <0.1 -- <0.05 <0.1 Cadmium -- <0.001 <0.001 -- <0.001 <0.001 0.001 <0.001 0.002 Chromium 0.001 <0.001 0.004 0.001(3) <0.001 <0.004 0.001(3) <0.001 <0.006 Cobalt 0.001(3) <0.001 <0.002 0.001(3) <0.001 <0.004 0.001 <0.001 0.005 Calcium 0.4 <0.4 1.2 0.4 <0.3 1.1 0.4 <0.3 1.7 Copper 0.31 0.03 0.83 0.20 <0.01 0.50 0.14 0.03 0.63 Iron 0.1(3) <0.1 <0.5 0.4 <0.05 3.3 0.2 <0.05 0.8 Lead 0.011 0.002 0.037 0.010 <0.001 0.039 0.010 <0.002 0.049 Lithium -- <0.001 <0.001 0.002(3) <0.001 <0.037 -- <0.001 <0.035 Manganese 0.01 <0.01 0.04 0.02 <0.01 0.17 0.01 <0.01 0.04 Molybdenum -- <0.01 <0.01 -- <0.01 <0.01 -- <0.01 <0.01 Nickel 0.003 <0.003 0.021 0.005(3) <0.002 <0.075 0.004(3) <0.002 <0.077 Silver -- <0.001 <0.001 -- <0.001 <0.001 -- <0.001 <0.001 Sodium 1.7(3) <0.3 <7.4 1.1 <0.3 5.7 1.1 <0.3 6.1 Thallium -- <0.001 <0.001 -- <0.001 <0.001 0.001 <0.001 0.001 Tin -- <0.01 <0.01 0.01 <0.01 0.02 -- <0.01 <0.01 Uranium -- <0.0011 <0.001 -- <0.0001 <0.001 -- <0.0001 <0.001 Vanadium 0.001 <0.001 0.003 0.002 <0.001 0.008 0.002 <0.001 0.010 Zinc 0.05 <0.05 0.1 0.04 <0.05 0.1 0.04 <0.05 0.1 Strontium 0.002 <0.003 0.004 0.002 <0.002 0.009 0.002 <0.002 0.004 Magnesium 0.2 <0.1 0.8 0.2 <0.1 0.9 0.2 <0.1 0.7 Potassium -- <0.3 <0.7 0.2(3) <0.3 <0.7 -- <0.3 <0.9 Sulphur -- <2.0 <2.2 1.1(3) <1.7 <2.8 1.0(3) <1.7 <2.3 Arsenic 0.001 <0.001 0.003 0.002 <0.001 0.005 0.003 <0.001 0.011 Selenium -- <0.001 <0.001 0.001(3) <0.001 <0.001 0.001 <0.001 0.001 Mercury -- <0.0001 <0.0001 -- <0.00005 <0.0001 -- <0.00005 <0.0001 Notes: (1) not detected values are reported at detection limit and are shown with a < symbol. (2) -- not applicable. (3) An average value has been reported because there was at least one detected value below the maximum method detection limit during the reporting period. Sampling for TSP/metals started on July 31st, 2002.

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TABLE 18 Summary of Year to Date PAH Results(1)

Victoria Road Frederick Street Henry Street Kings Road Intercolonial Street DesBarres Street Parameter Average

(ng/m3) Minimum

Value (ng/m3)

Maximum Value

(ng/m3) Average (ng/m3)

Minimum Value

(ng/m3)

Maximum Value

(ng/m3) Average (ng/m3)

Minimum Value

(ng/m3)

Maximum Value

(ng/m3) Average (ng/m3)

Minimum Value

(ng/m3)

Maximum Value

(ng/m3) Average (ng/m3)

Minimum Value

(ng/m3)

Maximum Value

(ng/m3) Average (ng/m3)

Minimum Value

(ng/m3)

Maximum Value

(ng/m3) Naphthalene 1.9 <0.07 15.4 1.4 <0.08 10.2 1.7 <0.07 10.6 1.3 <0.06 15.5 1.8 <0.08 13.1 1.4 <0.07 9.8 Acenaphthylene 0.8 <0.06 5.6 0.5 <0.06 3.2 1.3 <0.07 9.6 0.5 <0.06 4.8 0.7 <0.06 5.0 0.8 <0.06 6.3 Acenaphthene 0.5 <0.06 1.94 1.7 <0.07 10.0 0.56 <0.08 1.67 0.22 <0.06 0.83 1.0 0.18 2.8 0.62 <0.07 2.57 Fluorene 1.6 0.44 4.3 4 0.85 35 2.2 0.57 6.2 1.0 0.24 3.2 2.5 0.53 6.5 2.1 0.39 7.9 Phenanthrene 6.0 2.36 17.6 21 2.10 244 8.4 3.5 19.4 3.3 0.47 10.9 10 1.88 38 7.4 1.93 27.2 Anthracene 0.58 0.14 1.73 1.4 <0.07 16.5 1.0 0.28 3.4 0.31 <0.06 1.74 0.88 0.17 2.89 0.8 <0.08 5.1 Fluoranthene 1.3 0.43 4.6 3 0.41 32 2.2 0.62 6.6 0.68 <0.06 2.06 2.2 0.24 9.8 1.9 0.28 13.3 Pyrene 0.9 <0.13 3.7 1.5 0.23 12.1 2.0 0.54 7.1 0.52 <0.06 2.16 1.4 0.41 4.4 1.3 <0.08 9.8 Benzo(a)anthracene 0.2 <0.06 0.83 0.11 <0.04 0.38 0.29 <0.07 1.22 0.10 <0.06 0.61 0.14 <0.06 0.55 0.25 <0.06 2.53 Chrysene 0.22 <0.06 1.18 0.18 <0.04 0.62 0.46 <0.07 1.97 0.12 <0.04 0.69 0.21 <0.06 0.62 0.3 <0.06 4.1 Benzo Fluoranthene 0.7 <0.14 7.1 0.60 <0.01 2.78 0.9 <0.15 3.4 0.7 <0.02 6.6 0.5 <0.07 4.0 0.9 <0.01 5.7 Benzo(a)pyrene 0.13 <0.06 0.71 0.09 <0.04 0.34 0.24 <0.06 1.23 0.09 <0.06 0.48 0.12 <0.06 0.43 0.19 <0.06 1.43 Indeno(1,2,3-cd)pyrene 0.14 <0.06 0.56 0.10 <0.04 0.40 0.24 <0.06 1.07 0.09 <0.06 0.35 0.12 <0.06 0.38 0.17 <0.06 1.24 Dibenzo(a,h)anthracene 0.10 <0.06 0.47 --(3) <0.04 <0.14 0.08 <0.06 0.16 -- <0.06 <0.08 -- <0.06 <0.08 0.08 <0.06 0.38 Benzo(g,h,i)perylene 0.17 <0.06 0.63 0.10 <0.04 0.32 0.27 <0.06 1.15 0.09 <0.06 0.43 0.14 <0.06 0.54 0.16 <0.06 1.20 Total PAH (2) 15.2 -- -- 36 -- -- 21.8 -- -- 9.0 -- -- 22 -- -- 18.4 -- -- Notes: (1) not detected values are reported at detection limit and are shown with a < symbol. (2) Total PAH is the sum of all reported values, including PAHs with values reported as non-detect, using values at half the detection limit. (3) -- denotes not applicable.

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TABLE 19 Summary of Year to Date VOC Results(1)

Victoria Road Frederick Street Henry Street Kings Road Intercolonial Street DesBarres Street

Parameter

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Average (µµµµg/m3)

Minimum Value

(µµµµg/m3)

Maximum Value

(µµµµg/m3)

Dichlorodifluoromethane 1.58 <0.71 3.89 1.5(3) <0.7 <5.3 1.55(3) <0.71 <2.90 1.67 <0.71 3.89 1.65(3) <0.71 <3.18 1.6(3) <0.7 <4.6 Chloromethane 0.48(3) <0.60 <1.73 0.5(3) <0.6 <4.5 0.5 <0.6 2.3 0.44(3) <0.60 <1.86 0.48(3) <0.60 <2.68 0.6(3) <0.6 <3.7 Halocarbon 114 --(2) <0.92 <3.43 -- <1.1 <9.1 -- <1.03 <3.22 -- <0.92 <3.70 -- <0.92 <5.38 -- <1.1 <7.7 Vinyl chloride -- <0.20 <1.33 -- <0.2 <3.6 -- <0.20 <1.05 -- <0.20 <1.43 -- <0.20 <2.07 -- <0.2 <2.8 Chloroethane -- <0.24 <1.16 -- <0.2 <2.9 0.26(3) <0.24 <0.92 0.24(3) <0.24 <1.24 0.32 <0.24 2.08 0.29(3) <0.24 <2.51 1,2-Dichloroethane -- <0.61 <1.78 -- <0.6 <4.5 -- <0.61 <1.66 0.44(3) <0.61 <1.90 -- <0.61 <2.75 -- <0.61 <3.84 Bromomethane -- <0.35 <2.02 -- <0.3 <5.4 -- <0.35 <1.59 -- <0.35 <2.17 0.45(3) <0.35 <3.15 -- <0.3 <4.3 Trichlorofluoromethane 1.29 <0.79 2.42 1.3(3) <0.8 <6.2 1.26 <0.79 3.03 1.26 <0.79 2.83 1.4 <0.8 6.2 1.41(3) <0.79 <4.94 1,1-Dichloroethene -- <0.75 <2.18 0.6(3) <0.8 <5.6 -- <0.75 <2.02 -- <0.75 <2.34 -- <1 <3 -- <0.8 <4.8 cis-1,1-Dichloroethene -- <0.56 <2.18 -- <0.6 <5.6 -- <0.56 <1.74 -- <0.56 <2.34 -- <0.56 <3.41 -- <0.6 <4.8 1,1-Dichloroethane -- <0.69 <2.95 -- <0.7 <7.7 -- <0.69 <2.35 -- <0.69 <3.16 -- <0.69 <4.45 -- <0.7 <6.5 1,2-Dichloropropane -- <0.69 <2.54 -- <0.7 <6.5 -- <0.69 <2.03 -- <0.69 <2.73 -- <0.69 <3.97 -- <0.7 <5.5 Dichloromethane -- <1 <132 5.0(3) <0.8 <97.3 5(3) <1 <52 7(3) <1 <170 6(3) <1 <141 5(3) <1 <103 Chloroform -- <0.73 <2.15 -- <0.7 <5.4 -- <0.73 <2.05 -- <0.73 <2.29 -- <0.73 <3.32 -- <0.73 <4.64 1,1,2,2-Tetrachloroethane -- <1.17 <5.01 -- <1.5 <13.0 -- <1.31 <4.05 -- <1.17 <5.35 -- <1 <8 -- <1.5 <11.0 Halocarbon 113 0.86(3) <0.74 <3.37 1.1(3) <1.0 <8.4 0.91(3) <0.85 <2.91 0.97 <0.74 4.52 1.1 <0.7 8.4 1.3 <1.0 10.0 1,1,1-Trichloroethane 2.5 <0.8 12.0 2.2 <0.8 9.8 2.6 <0.8 13.6 2.5 <0.8 16.9 2.4 <0.8 11.5 4 <1 82 1,1,2-Trichloroethane -- <0.64 <2.40 -- <0.6 <6.0 -- <0.65 <1.91 -- <0.64 <2.56 -- <0.64 <3.71 -- <0.64 <5.18 Toluene 5.2 <0.5 17.7 4.0 <0.5 19.2 3.9 <0.5 18.1 4.3 <0.5 18.8 5 <0.5 23 4.0 <0.5 12.8 Benzene 1.9 <0.5 6.1 1.9 <0.5 8.9 2.0 <0.5 8.9 1.9 <0.5 6.7 2 <1 9 2.3 <0.5 10.2 cis-1,2-Dichloropropene -- <0.64 <2.36 -- <0.6 <6.4 -- <0.64 <1.86 -- <0.64 <2.54 -- <0.64 <3.68 -- <0.6 <5.0 trans-1,3-Dichloropropene -- <0.50 <2.22 -- <0.5 <5.9 -- <0.50 <1.77 -- <0.50 <2.41 -- <0.50 <3.49 -- <0.5 <5.0 Trichloroethene 6.7 <0.7 44.6 6.4 <0.7 38.2 6.5 <0.7 40.8 5.8 <0.7 40.8 6.7 <0.7 45.7 4.8 <0.7 35.5 Tetrachloroethene -- <0.81 <2.98 -- <1.0 <7.5 -- <0.92 <2.78 -- <0.81 <3.19 -- <0.81 <4.61 -- <1.02 <6.44 Carbon tetrachloride 0.70(3) <0.81 <2.77 -- <0.9 <6.9 -- <0.92 <2.58 -- <0.81 <2.96 -- <0.81 <4.28 -- <0.94 <5.98 Ethylene dibromide -- <0.81 <3.77 -- <1.0 <10.0 -- <0.92 <3.15 -- <0.81 <4.07 -- <0.81 <5.92 -- <1.0 <8.5 Ethylbenzene 0.8 <0.7 4.3 0.8(3) <0.7 <6.5 0.8 <0.7 3.9 0.9 <0.7 4.8 1(3) <1 <4 0.8(3) <0.7 <5.6 m&p-Xylene 2.6 <1.0 13.9 2.0 <1.0 10.0 2.1 <1.0 13.0 2.3 <1.0 12.2 2 <1 10 2.3 <1.0 10.0 o-Xylene 0.9 <0.8 3.9 0.8(3) <0.8 <6.5 0.9 <0.8 3.5 0.8 <0.8 3.5 1(3) <1 <4 0.9(3) <0.8 <5.6 1,3,5-Trimethylbenzene 1.15 <1.28 4.23 1.0(3) <1.3 <9.8 0.99(3) <1.28 <3.44 0.95(3) <1.28 <3.98 -- <1 <6 1.2 <1.3 9.8 1,2,4-Trimethylbenzene 2.0 <1.2 7.9 1.5(3) <1.2 <9.3 1.6 <1.2 6.9 1.4 <1.2 5.4 2 <1 8 1.6 <1.2 8.8 1,3-Dichlorobenzene -- <0.90 <4.39 1.3(3) <0.9 <11.4 -- <0.90 <4.09 -- <0.90 <4.69 -- <1 <7 -- <0.9 <9.6 1,4-Dichlorobenzene -- <0.90 <5.05 -- <0.9 <13.2 -- <0.90 <4.69 -- <0.90 <5.41 -- <1 <8 -- <0.9 <10.8 1,2-Dichlorobenzene -- <0.90 <5.05 -- <0.9 <13.2 -- <0.90 <4.69 -- <0.90 <5.41 -- <1 <8 -- <0.9 <10.8 1,2,4-Trichlorobenzene 1.7 1.0 <8.2 1.7(3) <1.1 <21.5 1.62(3) <0.95 <6.68 -- <0.8 <8.9 -- <1 <13 -- <1.1 <18.6 Hexachlorobutadiene -- <1.77 <10.24 -- <2.2 <26.7 -- <1.98 <9.49 -- <1.8 <10.7 -- <2 <16 -- <2.2 <22.4 Chlorobenzene 0.53(3) <0.69 <2.03 0.6(3) <0.7 <5.1 0.53(3) <0.69 <1.89 0.50(3) <0.69 <2.16 0.53(3) <0.69 <3.13 0.59(3) <0.69 <4.37 Notes: (1) not detected values are reported at detection limit and are shown with a < symbol. (2) -- not applicable. (3) An average value has been reported because there was at least one detected value below the maximum method detection limit during the reporting period.

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5.0 CONCLUSIONS Fixed station AAMP results for February 2003 were compared to available guidelines and standards that included the Nova Scotia Ambient Air Objective for TSP, the CWS for PM2.5, and the Ontario MOE AAQC for many of the remaining parameters. There were no exceedances to available 24-hour guidelines at the fixed sampling locations for the TSP, PM10, PM2.5, metals, PAH and VOC parameters during the month of February.

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6.0 REFERENCES AGRA Earth & Environmental Limited. Development of Interim Separation Zones, Former Coke

Ovens site, Sydney, Nova Scotia, 2000.

Environment Canada. Standard Reference Method for the Measurement of Suspended Particulate in the Atmosphere (High Volume Method). Report EPS 1-AP-73-2, January, 1973.

United States Environmental Protection Agency. Compendium Method TO13

Determination of Benzo(a)Pyrene and Other Polynuclear Aromatic Hydrocarbons (PAHs) in Ambient Air Using Gas Chromatographic and High Performance Liquid Chromatographic Analysis – Revision 1.0. New Jersey: Noyes Data Corporation, June 1998.

United States Environmental Protection Agency. Compendium Method TO-14A

Determination of Volatile Organic Compound (VOC) in Ambient Air Using Specially Prepared Canisters with Subsequent Analysis by Gas Chromatography. Cincinnati, OH: Center for Environmental Research Information, January 1999.

United States Environmental Protection Agency. Part II: National Ambient Air Quality Standards for Particulate Matter; Final Rule, 40 CFR part 50, Federal Register, Vol. 62, No. 138, 1997.

United States Environmental Protection Agency. Reference Method for the

Determination of Fine Particulate Matter as PM2.5 in the Atmosphere, 40 CFR, Subchapter C, Part 50 Appendix B, July 1997.

United States Environmental Protection Agency. Reference Method for the

Determination of Particulate Matter as PM10 in the Atmosphere, 40 CFR, Subchapter C, Part 50, Appendix M, July 1997.

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APPENDIX A

Sampling Equipment and Procedure Description

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PM10 Units Air sampling for PM10 is performed with a high volume sampler. Refer to Figure A1 for a sketch of the PM10 unit. The sampler consists of a size selective inlet, a filter holder, an air mover, a flow controller, and a timer. The unit works by drawing air into a size selective inlet at a flow rate, which is typically 40 ft3/min. Particles with aerodynamic diameters less than the cut point (less than 10 microns in diameter) are collected by the filter. The mass of the particles is determined by the difference in filter weights prior to and after sampling. The concentration of suspended particulate matter in the designated size range is calculated by dividing the weight gain of the filter by the volume of air sampled.

Figure A1

The main steps involved in sampling include the following:

1. Filter preparation by the Environmental Services Laboratory (ESL). 2. Installing the filter in the high volume sampler. 3. Setting the samplers timer so that it will turn on at midnight of the day of setup.

Checking the flow for a five-minute period to ensure the high volume sampler is operating properly. Inspecting the filter during the five-minute operation to ensure that the filter is installed correctly and is not damaged.

4. Performing periodic flow checks during the 24 hour sampling period to ensure the sampler is operating properly.

5. The sampler shuts off automatically after 24 hours (midnight) and AMEC collects the filter the following morning and transports it to ESL for PM10 and metals analysis. AMEC uses the field pressure measurements and laboratory results to calculate a concentration, which is reported in the monthly reports.

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PM2.5 Units Air sampling for PM2.5 in air is performed with a low volume sampler. Refer to Figure A2 for a sketch of the PM2.5 unit. The sampler consists of a size selective inlet, a filter holder, an air mover, a flow controller, and a timer. The unit works by drawing air into a size selective inlet at a flow rate, which is typically 16.7 L/min. Particles with aerodynamic diameters less than the cut point (less than 2.5 microns) are collected by the filter. The mass of the particles is determined by the difference in filter weights prior to and after sampling. The concentration of suspended particulate matter in the designated size range is calculated by dividing the weight gain of the filter by the volume of air sampled.

Figure A2

The main steps involved in sampling include the following:

1. Filter preparation by ESL. 2. Installing the filter in the low volume sampler 3. Setting the samplers timer so that it will turn on at midnight of the day of

setup. Checking the flow for a five-minute period to ensure the low volume sampler is operating properly.

4. Performing periodic flow checks during the 24 hour sampling period to ensure the sampler is operating properly.

5. The sampler shuts off automatically after 24 hours (midnight) and AMEC collects the filter the following morning and transports it to ESL for PM2.5 and metals analysis. AMEC uses the field pressure measurements and laboratory results to calculate a concentration, which is reported in the monthly reports.

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PAH Units Air sampling for PAHs in air is performed with a high volume sampler. Refer to Figure A3 for a sketch of the PAH unit. The sampler consists of a module containing a filter holder and polyurethane foam (PUF) backup media, an air mover, a flow controller, and a timer. The unit works by drawing air over a module at a flow rate, which is typically 7.9 ft3/min. PAH particulate matter is captured on a filter at the front of the PUF module, and the vapor phase of the PAHs is captured in the PUF foam backup.

Figure A3

The main steps involved in sampling include the following:

1. PUF module preparation by the ESL. 2. Installing the module in the high volume sampler 3. Setting the samplers timer so that it will turn on at midnight of the day of

setup. Checking the flow for a five-minute period to ensure the low volume sampler is operating properly.

4. Performing periodic flow checks during the 24 hour sampling period to ensure the sampler is operating properly.

5. The sampler shuts off automatically after 24 hours (midnight) and AMEC collects the module the following morning and transports it to ESL for PAH analysis. AMEC uses the field pressure measurements and laboratory results to calculate a concentration, which is reported in the monthly reports.

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Evacuated Canisters Air sampling for VOCs in air is performed with an evacuated canister. The sampler consists of a stainless steel canister, and a sampling tip with a flow restrictive orifice. The unit works by drawing in air through the evacuation of the canister (under negative pressure) through the flow restrictive orifice filling the 1.7 litre canister over a 24 hour period. VOCs will be captured in the canister, where they are analyzed at Phillip Analytical Laboratories in Burlington, Ontario.

Figure A4

The main steps involved in sampling include the following:

1. VOC canister preparation by Phillip Analytical Laboratory. 2. Installing the VOC canister at the sampling location and attaching the flow

restrictive tip. 3. Checking the initial pressure of the canister to ensure it is useable for sampling. 4. Manually opening the canister valve at midnight on the day of sampling to start

the evacuation (sampling) process. 5. Manually closing the canister valve the following midnight (24 hours later) on the

day sampling is complete in order to end the evacuation process. 6. Checking the final pressure in the canister to ensure that a complete sample was

obtained. 7. AMEC collects the canister the following morning and ships it to PSC for VOC

analysis. AMEC receives the laboratory results, which are converted to µg/m3, and are then reported in the monthly reports.

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APPENDIX B

Data Validation Report

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Memo

To Bill Chew File no From Marilyn Hoyt and Karen Hamill cc Date March 31, 2003

Peter Lund

Subject Muggah Creek Air Monitoring

Draft Data Validation Report – February Sampling Events INTRODUCTION Data for the analyses of air samples collected during February 2003 in support of the Muggah Creek Remediation Project in Sydney, Nova Scotia have been reviewed. These samples were collected on February 8 and 20, 2003 at the program’s established monitoring locations in Sydney, Nova Scotia. Samples included in this review are listed in Table 1. Samples were collected in evacuated canisters for analyses for volatile organic compounds (VOC) in accordance with U. S. EPA Method TO-14A; for polyaromatic hydrocarbons (PAH) on glass fiber filters and polyurethane foam plugs (PUF) in accordance with Method TO13A; and for metals on quartz filters. Metals samples included the collection of filters for total suspended particulate (TSP) as well as particulate matter with aerodynamic diameters of 10 microns or less (PM10) on quartz fiber filters. Particulate matter with a diameter of 2.5 microns or less (PM2.5) was collected this month on PTFE Teflon Membrane Filters. Philip Analytical Services (PSC) of Burlington, Ontario conducted analyses for VOC, Environmental Services Laboratory (ESL) of Sydney, Nova Scotia conducted analyses for PAH, particulates (TSP, PM10) and metals, and the Chester LabNET in Tigard, Oregon conducted the analyses for the PM2.5. Data validation was conducted based upon reported results for quality control/quality assurance measures and consistent with U.S. EPA guidance for data review and evaluation. SUMMARY OF VALIDATION FINDINGS Results for volatile organics, PAH and metals have been validated. Quality assurance/quality control measures met or exceeded method requirements with exceptions as discussed in the report. Although individual data points have been qualified for a variety of quality-assurance related issues, results as included in the final validated set are appropriate for use in characterizing the quality of the airshed in Sydney, Nova Scotia during the monitoring events. Qualifications to results are summarized below: Volatile Organics ! Most volatiles detected were at concentrations less than one half the low calibration

standard and are qualified as estimated (JC) since the linearity of the instrument response cannot be assumed.

! Results for dichloromethane (methylene chloride) have been qualified as non-detected with elevated reporting limits as a result of laboratory background (UB).

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Validated data for VOC are presented in Tables 2 and 3. Table 5 presents data for the analyses of field duplicate samples by PSC and Environment Canada. PAH Results for naphthalene from the February 8, 2003 sampling event are qualified as estimated with potential low bias as a result of recoveries below 60% from the matrix spike samples. Naphthalene was also present in the February 8, 2003 field blank, but at a trace level that affected only the Kings Road sample result. Naphthalene was also present in the method blank for the February 20, 2003; results for all samples in this set except the Henry Street sample were qualified as non-detected with elevated reporting limits. Validated data for PAH are presented in Tables 5 and 6. Results for field duplicates are presented in Table 7. Metals and Particulates Results for metals and particulates are presented in Tables 8 through 10. No metals were detected in the Method Blanks or Field Blanks for the PM10 and TSP samples. Gravimetric results for TSP for the Victoria Road sample on February 20th were rejected since the mass of individual metals reported exceeded the reported TSP. The TSP result for Henry Street is considered biased low because the PM2.5 result is higher than the TSP result. The TSP result could not be rejected because the mass of individual metals does not exceed the TSP value. REVIEW ELEMENTS Data validation included review and evaluation of the following elements:

1. Sampling records 2. Chain of Custody documentation 3. Holding times 4. Canister certification analyses (VOC samples) 5. Canister pressure after sampling and upon laboratory receipt (VOC samples) 6. Method blanks 7. Laboratory spike samples 8. Matrix spike samples 9. Sample duplicate analyses 10. Internal Standard recoveries (VOC) 11. Surrogate recoveries (PAH) 12. Field blanks

Only those areas where discrepancies or anomalous results were noted are discussed below. The attached data tables indicate specific samples affected by these instances. VOLATILE ORGANIC ANALYSES

Method Blank and Canister Certification Analyses Dichloromethane was detected in the method blanks and certification analyses at concentrations ranging up to 0.68 ppbv. U.S. EPA guidance followed for this review directs that data for common laboratory chemicals such as dichloromethane be qualified unless the analyte is detected at 10

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times above the level in the associated blanks. Unless this is the case, sample analysis results are considered potentially attributable to the laboratory background and dichloromethane is reported as non-detected with reporting limits set at the concentrations actually detected during the analyses (UB). PSC flagged all dichloromethane results as potentially attributable to laboratory background. Dichloromethane in all samples has been qualified as non-detected (UB) with reporting limits set at the concentrations detected in the individual samples.

Canister Pressure Readings The pressure of the canister is measured in the field at the end of the sampling event and then again by the laboratory prior to analysis. Sampling flows are designed so that canisters will still be at negative pressure (under vacuum) at the end of each sampling event. The readings at the laboratory are taken to confirm that in-leakage of air through the valve has not occurred during shipment or storage. There were no pressure anomalies for samples collected in February 2003.

Matrix Spike Analysis The matrix spikes prepared and analyzed with the field samples demonstrated recoveries within acceptance limits. Internal Standards Internal standards added to samples are used to quantify detected target analytes. Their recovery is monitored as a measure of the overall accuracy of the analysis. All internal standards recoveries were within acceptance limits. Field Duplicates and Quality Control Analyses by Environment Canada Field duplicate samples were collected at the Intercolonial Street location on February 20, 2003. Results for the analyses at PSC and Environment Canada (EC) are presented in Table 4. All detected analytes present were below ½ the low calibration standard at PSC and are qualified as estimated. Concentrations reported by EC were consistently higher by a factor of approximately two. The EC analyses are conducted using a different technique that provides lower detection limits for target analytes; differences in results between the two laboratories near or at the PSC reporting limits are within method expectations. PAH ANALYSES The recovery of naphthalene for the matrix spike associated with the February 8, 2003 samples was 55%, below the method control limit of 60%. Results for naphthalene in these samples are qualified as estimated with a potential low bias. In addition, the field blank collected February 8, 2003 contained a trace level (0.09 µg) of naphthalene. Naphthalene in all samples except the Kings Road sample was greater than 10 times above the level in the associated blanks; the result for Kings Road was qualified as non-detected with an elevated reporting limit and data for other samples were accepted with qualification as noted above. The method blank for the February 20, 2003 samples contained naphthalene at a concentration such that results for all samples except the Henry Street sample could potentially be attributed to background laboratory contamination. Results have been qualified as non-detected with reporting limits set at the concentrations noted in the individual samples.

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Field duplicate PAH results as presented in Table 7. Results for the Frederick Street samples on February 20, 2003 demonstrated acceptable agreement for all analytes. METALS ANALYSES Method and Field Blanks Method and field blanks for the analyses of quartz filters were reported to have no detectable metals. Gravimetric Analyses – PM2.5, PM10 and TSP Both field blanks for PM10 and TSP on February 8, 2003 contained trace levels of particulate. Sample results were all greater than 10 times the blank, so results have not been qualified. Results for TSP for the Victoria Road sample on February 20, 2003 were rejected. The total mass of metals reported for this filter exceeded the TSP mass, indicating either a laboratory error or a possible tear or loss of a small fragment of the filter material. Results for TSP for the February 20, 2003 Henry Street sample are considered biased low (BL) since the PM2.5 result is anomously higher than the TSP result for the same location.

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Table 1: Air Samples in February 2003

Muggah Creek Remediation ProjectSydney, Nova Scotia

Location Analysis February 8, 2003 February 20, 20031 Victoria Road VOC 1090-V-33-L1-080203-AC-M46 1115-V-33-L1-200203-AC-M02

PAH 1096-P-33-L1-080203-AC-G 1122-P-33-L1-200203-AC-DMetals, PM10 1103-10-33-L1-080203-AC-Q013596 1129-10-33-L1-200203-AC-Q013541TSP 1107-TSP-33-L1-080203-AC-Q013562 1133-TSP-33-L1-200203-AC-Q013545

2 Frederick Street VOC 1091-V-33-L2-080203-AC-M26 1116-V-33-L2-200203-AC-M11PAH 1097-P-33-L2-080203-AC-T 1123-P-33-L2-200203-AC-1Metals, PM10 1104-10-33-L2-080203-AC-Q013597 1130-10-33-L2-200203-AC-Q013542TSP 1108-TSP-33-L2-080203-AC-Q013563 1134-TSP-33-L2-200203-AC-Q013546

3 Henry Street VOC 1092-V-33-L3-080203-AC-M14 1117-V-33-L3-200203-AC-M41PAH 1098-P-33-L3-080203-AC-27 1124-P-33-L3-200203-AC-27Metals, PM2.5 1111-25-33-L3-080203-AC-6520 1136-25-33-L3-200203-AC-6522TSP 1109-TSP-33-L3-080203-AC-Q013564 1135-TSP-33-L3-200203-AC-Q013566

4 Kings Road VOC 1094-V-33-L4-080203-AC-M31 1119-V-33-L4-200203-AC-M47PAH 1100-P-33-L4-080203-AC-23 1125-P-33-L4-200203-AC-23Metals, PM2.5 1112-25-33-L4-080203-AC-6521 1137-25-33-L4-200203-AC-6523

5 Intercolonial Street VOC 1093-V-33-L5-080203-AC-M04 1118-V-33-L5-200203-AC-M31PAH 1099-P-33-L5-080203-AC-D 1126-P-33-L5-200203-AC-GMetals, PM2.5 1113-25-33-L5-080203-AC-6542 1138-25-33-L5-200203-AC-6524

6 DesBarres Street VOC 1095-V-33-L6-080203-AC-M28 1120-V-33-L6-200203-AC-M24PAH 1101-P-33-L6-080203-AC-24 1127-P-33-L6-200203-AC-24Metals, PM10 1105-10-33-L6-080203- AC-Q013560 1131-10-33-L6-200203- AC-Q013543

Field Blank VOCPAH 1102-P-33-L1-080203-AC-1 AMetals, PM10 1106-10-33-L2-080203-AC-Q013561 AMetals, PM2.5 1114-25-33-L4-080203-AC-6543 ATSP 1110-TSP-33-L3-080203-AC-Q013565 A

Field Duplicate VOC 1121-V-33-L5 -200203-AC-M39 BPAH 1128-P-33-L2-200203-AC-T BMetals, PM10 1132-10-33-L1-200203-AC-Q013544 BMetals, PM2.5TSP

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Table 2: Validated Data for Volatile Organics in AirMuggah Creek Remediation Program

February 8, 2003 Sampling EventSydney, Nova Scotia

Victoria Road Frederick Street Henry Street Kings Road Intercolonial Street DesBarres Street

1090-V-33-L1-080203-AC-M46

1091-V-33-L2-080203-AC-M26

1092-V-33-L3-080203-AC-M14

1094-V-33-L4-080203-AC-M31

1093-V-33-L5-080203-AC-M04

1095-V-33-L6-080203-AC-M28

005776 03 005777 03 005778 03 005780 03 005779 03 005781 0308-Feb-2003 08-Feb-2003 08-Feb-2003 08-Feb-2003 08-Feb-2003 08-Feb-2003

ppbv ppbv ppbv ppbv ppbv ppbvDichlorodifluoromethane 0.24JC 0.22JC 0.21JC 0.23JC 0.20JC <0.42UChloromethane <0.29U <0.29U <0.29U <0.29U <0.29U <0.61UHalocarbon 114 <0.17U <0.17U <0.17U <0.17U <0.17U <0.36UVinyl Chloride <0.18U <0.18U <0.18U <0.18U <0.18U <0.38UChloroethane <0.15U <0.15U <0.15U <0.15U <0.15U <0.32U1,2-Dichloroethane <0.15U <0.15U <0.15U <0.15U <0.15U <0.32UBromomethane <0.18U <0.18U <0.18U <0.18U <0.18U <0.38UTrichlorofluoromethane <0.14U <0.14U <0.14U <0.14U <0.14U <0.29U1,1-Dichloroethylene <0.19U <0.19U <0.19U <0.19U <0.19U <0.40Ucis-1,2-dichloroethylene <0.19U <0.19U <0.19U <0.19U <0.19U <0.40U1,1-Dichloroethane <0.25U <0.25U <0.25U <0.25U <0.25U <0.53U1,2-Dichloropropane <0.19U <0.19U <0.19U <0.19U <0.19U <0.40UDichloromethane <0.72UB <0.22U <0.42UB <0.22U <0.22U <0.76UBChloroform <0.15U <0.15U <0.15U <0.15U <0.15U <0.32U1,1,2,2-Tetrachloroethane <0.25U <0.25U <0.25U <0.25U <0.25U <0.53UHalocarbon 113 <0.15U <0.15U <0.15U <0.15U <0.15U <0.32U1,1,1-Trichloroethane <0.14U <0.14U <0.14U <0.14U 0.15JC <0.29U1,1,2-Trichloroethane <0.15U <0.15U <0.15U <0.15U <0.15U <0.32UToluene <0.13U <0.13U 0.13JC <0.13U <0.13U <0.27UBenzene 0.22JC <0.18U 0.20JC <0.18U 0.28JC 1.1JCcis-1,3-Dichloropropene <0.18U <0.18U <0.18U <0.18U <0.18U <0.38Utrans-1,3-Dichloropropene <0.17U <0.17U <0.17U <0.17U <0.17U <0.36UTrichloroethylene <0.17U <0.17U <0.17U <0.17U <0.17U <0.36UTetrachloroethylene <0.15U <0.15U <0.15U <0.15U <0.15U <0.32UCarbon tetrachloride <0.15U <0.15U <0.15U <0.15U <0.15U <0.32UEthylene Dibromide <0.17U <0.17U <0.17U <0.17U <0.17U <0.36UEthylbenzene <0.2U <0.2U <0.2U <0.2U <0.2U <0.4UM&P-Xylene <0.23U <0.23U <0.23U <0.23U <0.23U <0.48UO-Xylene <0.2U <0.2U <0.2U <0.2U <0.2U <0.4U1,3,5-Trimethylbenzene <0.26U <0.26U <0.26U <0.26U <0.26U <0.55U1,2,4-Trimethylbenzene <0.25U <0.25U <0.25U <0.25U <0.25U <0.53U1,3-Dichlorobenzene <0.25U <0.25U <0.25U <0.25U <0.25U <0.53U1,4-Dichlorobenzene <0.29U <0.29U <0.29U <0.29U <0.29U <0.61U1,2-Dichlorobenzene <0.29U <0.29U <0.29U <0.29U <0.29U <0.61U1,2,4-Trichlorobenzene <0.39U <0.39U <0.39U <0.39U <0.39U <0.82UHexachlorobutadiene <0.33U <0.33U <0.33U <0.33U <0.33U <0.69UChlorobenzene <0.15U <0.15U <0.15U <0.15U <0.15U <0.32UStyrene <2.0U <2.0U <2.0U <2.0U <2.0U <4.2UU = Non-detected at stated limit.UB = Non-detected with elevated reporting limit as a result of background laboratory and/or canister contamination.JC = Estimated value, measured at less than 1/2 the low calibration standard.

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Table 3: Validated Data for Volatile Organics in AirMuggah Creek Remediation Program

February 20, 2003 Sampling EventSydney, Nova Scotia

Victoria Road Frederick Street Henry Street Kings Road Intercolonial StreetIntercolonial Street

Field Duplicate DesBarres Street1115-V-33-L1-200203-AC-

M021116-V-33-L2-200203-AC-

M111117-V-33-L3-200203-AC-

M411119-V-33-L4-200203-AC-

M471118-V-33-L5-200203-AC-

M311121-V-33-L5-200203-AC-

M39B1120-V-33-L6-200203-AC-

M24007597 03 007598 03 007599 03 007600 03 007601 03 007603 03 007602 03

20-Feb-2003 20-Feb-2003 20-Feb-2003 20-Feb-2003 20-Feb-2003 20-Feb-2003 20-Feb-2003ppbv ppbv ppbv ppbv ppbv ppbv ppbv

Dichlorodifluoromethane <0.20U <0.20U <0.34U 0.21JC <0.32U 0.40JC <0.20UChloromethane <0.29U <0.29U <0.49U <0.29U <0.46U <0.52U <0.29UHalocarbon 114 <0.17U <0.17U <0.29U <0.17U <0.27U <0.31U <0.17UVinyl Chloride <0.18U <0.18U <0.31U <0.18U <0.29U <0.32U <0.18UChloroethane <0.15U <0.15U <0.26U <0.15U <0.26U <0.27U <0.15U1,2-Dichloroethane <0.15U <0.15U <0.26U <0.15U <0.26U <0.27U <0.15UBromomethane <0.18U <0.18U <0.31U <0.18U <0.29U <0.32U <0.18UTrichlorofluoromethane <0.14U <0.14U <0.24U <0.14U <0.24U <0.25U <0.14U1,1-Dichloroethylene <0.19U <0.19U <0.32U <0.19U <0.30U <0.34U <0.19Ucis-1,2-dichloroethylene <0.19U <0.19U <0.32U <0.19U <0.30U <0.34U <0.19U1,1-Dichloroethane <0.25U <0.25U <0.43U <0.25U <0.40U <0.45U <0.25U1,2-Dichloropropane <0.19U <0.19U <0.32U <0.19U <0.30U <0.34U <0.19UDichloromethane <0.22U <0.22U <0.85UB <0.53UB <0.94UB <1.2UB <0.47UBChloroform <0.15U <0.15U <0.26U <0.15U <0.24U <0.27U <0.15U1,1,2,2-Tetrachloroethane <0.25U <0.25U <0.43U <0.25U <0.40U <0.45U <0.25UHalocarbon 113 0.17JC <0.15U <0.26U <0.15U <0.24U <0.27U <0.15U1,1,1-Trichloroethane <0.14U <0.14U <0.24U <0.14U 0.27JC <0.25U 0.16JC1,1,2-Trichloroethane <0.15U <0.15U <0.26U <0.15U <0.24U <0.27U <0.15UToluene 0.14JC <0.13U 0.60JC <0.13U 0.30JC 0.45JC <0.13UBenzene 0.28JC <0.18U 0.51JC 0.26JC 0.35JC <0.32U 0.28JCcis-1,3-Dichloropropene <0.18U <0.18U <0.31U <0.18U <0.29U <0.32U <0.18Utrans-1,3-Dichloropropene <0.17U <0.17U <0.29U <0.17U <0.27U <0.31U <0.17UTrichloroethylene <0.17U <0.17U <0.29U <0.17U <0.27U <0.31U <0.17UTetrachloroethylene <0.15U <0.15U <0.26U <0.15U <0.24U <0.27U <0.15UCarbon tetrachloride <0.15U <0.15U <0.26U <0.15U <0.24U <0.27U <0.15UEthylene Dibromide <0.17U <0.17U <0.29U <0.17U <0.27U <0.31U <0.17UEthylbenzene <0.2U <0.2U <0.3U <0.2U <0.3U <0.3U <0.2UM&P-Xylene <0.23U <0.23U <0.39U <0.23U <0.37U <0.41U <0.23UO-Xylene <0.2U <0.2U <0.3U <0.2U <0.3U <0.3U <0.2U1,3,5-Trimethylbenzene <0.26U <0.26U <0.44U <0.26U <0.42U <0.47U <0.26U1,2,4-Trimethylbenzene <0.25U <0.25U <0.43U <0.25U <0.40U <0.45U <0.25U1,3-Dichlorobenzene <0.25U <0.25U <0.43U <0.25U <0.40U <0.45U <0.25U1,4-Dichlorobenzene <0.29U <0.29U <0.49U <0.29U <0.46U <0.52U <0.29U1,2-Dichlorobenzene <0.29U <0.29U <0.49U <0.29U <0.46U <0.52U <0.29U1,2,4-Trichlorobenzene <0.39U <0.39U <0.66U <0.39U <0.62U <0.70U <0.39UHexachlorobutadiene <0.33U <0.33U <0.56U <0.33U <0.53U <0.59U <0.33UChlorobenzene <0.15U <0.15U <0.26U <0.15U <0.24U <0.27U <0.15UStyrene <2.0U <2.0U <3.4U <2.0U <3.2U <3.6U <2.0UU = Non-detected at stated limit.UB = Non-detected with elevated reporting limit as a result of background laboratory and/or canister contamination.JC = Estimated value, measured at less than 1/2 the low calibration standard.

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Table 4: Field Duplicates for Volatile Organics in AirFebruary 2003

Muggah Creek Remediation ProgramSydney, Nova Scotia

Intercolonial Street

Intercolonial Street Field Duplicate

1118-V-33-L5-200203-AC-M31

1121-V-33-L5-200203-AC-M39B

EC 007601 03 007603 03 PSCKC-M31 KC-M39 RPD 20-Feb-2003 20-Feb-2003 RPD

ppbv ppbv ppbv ppbvFreon 12 (Dichlorodifluoromethane) 0.717 0.833 15% <0.32U 0.40JC 100%Chloromethane 0.561 0.544 3% <0.46U <0.52UDichloromethane 2.093 2.568 20% <0.94UB <1.2UB1,1,1-Trichloroethane 0.596 0.383 43% 0.27JC <0.25U 75%Benzene 0.618 0.416 39% 0.35JC <0.32U 55%Trichloroethylene 0.379 0.300 23% <0.27U <0.31UToluene 0.891 1.199 30% 0.30JC 0.45JC 40% 99% 85%

U = Non-detected at the stated limit.JC = Estimated value; measured at less than 1/2 the low calibration standardRPD = Relative percent difference

Environment Canada (EC)EC/PSC

RPD

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Table 5: Validated Data for PAH in AirFebruary 8, 2003 Sampling Event

Muggah Creek Remediation ProgramSydney, Nova Scotia

Victoria Road Frederick Street Henry Steet Kings Road Intercolonial Street DesBarres Street Victoria Road Field Blank

1096-P-33-L1-080203-AC-G

1097-P-33-L2-080203-AC-T

1098-P-33-L3-080203-AC-27

1100-P-33-L4-080203-AC-23

1099-P-33-L5-080203-AC-D

1101-P-33-L6-080203-AC-24

1102-P-33-L1-080203-AC-1A

µg/sample µg/sample µg/sample µg/sample µg/sample µg/sample

Naphthalene-PUF 1.4JM 1.0JM 4.0JM 0.35UB 1.3JM 1.4JM 0.09JMAcenaphthylene-PUF 0.45 0.9 2.8 0.08 0.39 0.35 <0.05UAcenaphthene-PUF 0.22 0.29 0.63 0.05 0.32 0.26 <0.05UFluorene-PUF 0.78 0.95 1.4 0.28 0.77 0.59 <0.05UPhenanthrene-PUF 1.9 2.5 5.0 0.75 2.1 1.9 <0.05UAnthracene-PUF 0.19 0.28 0.90 0.05 0.19 0.16 <0.05UFluoranthene-PUF 0.37 0.86 1.7 0.15 0.38 0.40 <0.05UPyrene-PUF 0.33 0.73 1.5 0.12 0.30 0.32 <0.05UBenzo(a)anthracene-PUF 0.07 0.14 0.46 <0.05U 0.08 0.13 <0.05UChrysene-PUF 0.11 0.18 0.46 <0.05U 0.11 0.14 <0.05UBenzo Fluoranthene-PUF 0.18 0.32 0.79 <0.1U 0.19 0.22 <0.1UBenzo(a) pyrene-PUF 0.06 0.11 0.33 <0.05U 0.06 0.09 <0.05UIndeno (1,2,3-cd) pyrene-PUF 0.10 0.16 0.35 <0.05U 0.10 0.10 <0.05UDibenz(a,h,) anthracene-PUF <0.05U <0.05U 0.05 <0.05U <0.05U <0.05U <0.05UBenzo(g.h,i)perylene-PUF 0.11 0.12 0.28 <0.05U 0.09 0.08 <0.05USurrogate, % recoveryAcenaphthene-d10 - PUF 85 66 77 65 90 86 74Phenanthrene-d10 - PUF 90 74 85 83 125 97 78Chrysene-d12 - PUF 93 73 82 90 134 98 87

JM = Estimated value; recovery from matrix spike indicates potential low bias.

UB = Non-detected with elevated reporting limit as a result of method and/or field blank contamination.U = Non-detected at the stated limit.

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Table 6: Validated Data for PAH in AirFebruary 20, 2003 Sampling Event

Muggah Creek Remediation ProgramSydney, Nova Scotia

Victoria Road Frederick Street Frederick Street Field Duplicate Henry Steet Kings Road Intercolonial Street DesBarres Street

1122-P-33-L1-200203-AC-D

1123-P-33-L2-200203-AC-1

1128-P-33-L2-200203-AC-TB

1124-P-33-L3-200203-AC-27

1125-P-33-L4-200203-AC-23

1126-P-33-L5-200203-AC-G

1127-P-33-L6-200203-AC-24

µg/sample µg/sample µg/sample µg/sample µg/sample µg/sample µg/sample

Naphthalene-PUF 0.34UB 0.19UB 0.17UB 1.1 0.28UB 0.38UB 0.36UBAcenaphthylene-PUF 0.34 0.23 0.20 2.4 0.12 0.33 1.1Acenaphthene-PUF 0.16 0.31 0.34 0.23 0.06 0.17 0.25Fluorene-PUF 0.86 0.89 0.82 2.1 0.31 0.84 1.3Phenanthrene-PUF 2.1 1.8 1.5 7.4 1.0 1.8 4.4Anthracene-PUF 0.14 0.12 0.12 1.3 0.06 0.13 0.47Fluoranthene-PUF 0.32 0.29 0.25 2.5 0.18 0.28 1.4Pyrene-PUF 0.29 0.26 0.22 2.7 0.13 0.26 1.2Benzo(a)anthracene-PUF <0.05U <0.05U <0.05U 0.4 <0.05U <0.05U 0.26Chrysene-PUF 0.07 0.08 0.07 0.75 <0.05U 0.06 0.32Benzo Fluoranthene-PUF 0.11 0.11 0.1 1.0 <0.1U <0.1U 0.43Benzo(a) pyrene-PUF <0.05U <0.05U <0.05U 0.38 <0.05U <0.05U 0.18Indeno (1,2,3-cd) pyrene-PUF <0.05U <0.05U <0.05U 0.38 <0.05U <0.05U 0.16Dibenz(a,h,) anthracene-PUF <0.05U <0.05U <0.05U 0.06 <0.05U <0.05U <0.05UBenzo(g.h,i)perylene-PUF 0.07 0.05 0.05 0.41 <0.05U <0.05U 0.13Surrogate, % recoveryAcenaphthene-d10 - PUF 71 75 83 62 79 83 78Phenanthrene-d10 - PUF 88 92 82 89 83 83 86Chrysene-d12 - PUF 94 97 84 91 91 91 87

UB = Non-detected with elevated reporting limit as a result of method and/or field blank contamination.U = Non-detected at the stated limit.

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Table 7: Field Duplicate Samples for PAH in AirFebruary, 2003

Muggah Creek Remediation ProgramSydney, Nova Scotia

Frederick Street Frederick Street Field Duplicate

1123-P-33-L2-200203-AC-1

1128-P-33-L2-200203-AC-TB RPD

µg/sample µg/sampleNaphthalene-PUF 0.19UB 0.17UBAcenaphthylene-PUF 0.23 0.2 14%Acenaphthene-PUF 0.31 0.34 9%Fluorene-PUF 0.89 0.82 8%Phenanthrene-PUF 1.8 1.5 18%Anthracene-PUF 0.12 0.12 0%Fluoranthene-PUF 0.29 0.25 15%Pyrene-PUF 0.26 0.22 17%Benzo(a)anthracene-PUF <0.05U <0.05U Chrysene-PUF 0.08 0.07 13%Benzo Fluoranthene-PUF 0.11 0.1 10%Benzo(a) pyrene-PUF <0.05U <0.05U Indeno (1,2,3-cd) pyrene-PUF <0.05U <0.05U Dibenz(a,h,) anthracene-PUF <0.05U <0.05UBenzo(g.h,i)perylene-PUF 0.05 0.05 0%

RPD = relative percent difference

U = Non-detected at the stated limit.UB = Non-detected with elevated reporting limit as a result of method and/or field blank contamination.

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Table 8: Validated Data for Metals in AirFebruary 8, 2003 Sampling Event

Muggah Creek Remediation ProgramSydney, Nova Scotia

Victoria Road Frederick Street DesBarres Street Frederick Street Victoria Road Frederick Street Henry Street Henry Street Field Blank

Field Blank

1103-10-33-L1-080203-AC-Q013596

1104-10-33-L2-080203-AC-Q013597

1105-10-33-L6-080203-AC-Q013560

1106-10-33-L2-080203-AC-Q013561A

1107-TSP-33-L1-080203-AC-Q013562

1108-TSP-33-L2-080203-AC-Q013563

1109-TSP-33-L3-080203-AC-Q013564

1110-TSP-33-L3-080203-AC-Q013565A

mg/filter mg/filter mg/filter mg/filter mg/filter mg/filter mg/filter mg/filterAluminum - Filter <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2UAntimony - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UBarium - Filter <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02UBeryllium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UBoron - Filter <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1UCadmium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UChromium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UCobalt - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UCalcium - Filter <0.7U <0.7U <0.7U <0.7U <0.7U <0.7U <0.7U <0.7U <0.7UCopper - Filter <0.02U <0.02U 0.02 <0.02U <0.02U 0.05 0.03 0.06 <0.02UIron - Filter <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1ULead - Filter <0.002U <0.002U 0.003 <0.002U <0.002U 0.003 <0.002U 0.005 <0.002ULithium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UManganese - Filter <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02UMolybdenum - Filter <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02UNickel - Filter <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005USilver - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002USodium - Filter <0.6U <0.6U <0.6U <0.6U <0.6U <0.6U <0.6U <0.6U <0.6UThallium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UTin - Filter <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02UUranium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UVanadium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UZinc - Filter <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1UStrontium - Filter <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005UMagnesium - Filter <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2UPotassium - Filter <0.6U <0.6U <0.6U <0.6U <0.6U <0.6U <0.6U <0.6U <0.6USulfur - Filter <3.7U <3.7U <3.7U <3.7U <3.7U <3.7U <3.7U <3.7U <3.7UArsenic - Filter <0.002U <0.002U 0.003 0.003 <0.002U <0.002U <0.002U 0.012 <0.002USelenium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UMercury - Filter <0.0001U <0.0001U <0.0001U <0.0001U <0.0001U <0.0001U <0.0001U <0.0001U <0.0001U

Particulates 14.4 10.4 15.3 1.1 24.1 23.8 28 1.1U = Non-detect at stated limit.

PM10, mg/Filter TSP, mg/filter

February 8, 2003 Quartz Filter Blank

TSP, mg/filterPM10, mg/filter

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Table 9: Validated Data for Metals in AirFebruary 20, 2003 Sampling Event

Muggah Creek Remediation ProgramSydney, Nova Scotia

Victoria Road Victoria Road Frederick Street DesBarres Street Victoria Road Frederick Street Henry StreetField Duplicate

1129-10-33-L1-200203-AC-Q013541

1132-10-33-L1-200203-AC-Q013544B

1130-10-33-L2-200203-AC-Q013542

1131-10-33-L6-200203-AC-Q013543

1133-TSP-33-L1-200203-AC-Q013545

1134-TSP-33-L2-200203-AC-Q013546

1135-TSP-33-L3-200203-AC-Q013566

mg/filter mg/filter mg/filter mg/filter mg/filter mg/filter mg/filterAluminum - Filter <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2UAntimony - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UBarium - Filter <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02UBeryllium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UBoron - Filter <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1U <0.1UCadmium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UChromium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UCobalt - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UCalcium - Filter <0.7U <0.7U <0.7U <0.7U <0.7U <0.7U <0.7U <0.7UCopper - Filter <0.02U 0.08 0.22 0.05 0.03 0.64 0.5 0.36Iron - Filter <0.1U <0.1U <0.1U 0.1 <0.1U 0.1 0.3 0.1Lead - Filter <0.002U 0.006 0.006 0.007 0.01 0.011 0.013 0.023Lithium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UManganese - Filter <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02UMolybdenum - Filter <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02U <0.02UNickel - Filter <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005USilver - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002USodium - Filter <0.6U 0.7 <0.6U <0.6U <0.6U 2.2 1.2 1.1Thallium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UTin - Filter <0.02U <0.02U <0.02U <0.02U 0.02 <0.02U <0.02U <0.02UUranium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UVanadium - Filter <0.002U <0.002U 0.002 0.003 0.002 0.002 0.006 0.006Zinc - Filter <0.1U <0.1U <0.1U <0.1U <0.1U 0.1 <0.1U <0.1UStrontium - Filter <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005U <0.005UMagnesium - Filter <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2U <0.2UPotassium - Filter <0.6U <0.6U <0.6U <0.6U <0.6U <0.6U <0.6U <0.6USulfur - Filter <3.7U <3.7U <3.7U <3.7U <3.7U <3.7U <3.7U <3.7UArsenic - Filter <0.002U <0.002U 0.002 0.004 0.018 0.002 0.006 0.022Selenium - Filter <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002U <0.002UMercury - Filter <0.0001U <0.0001U <0.0001U <0.0001U <0.0001U <0.0001U <0.0001U <0.0001U

Particulates 1.3 3 5.2 3.5 2.1 R 17.7 5BLU = Non-detect at stated limit.

PM10, mg/filter

R = Rejected; see text of report for discussion.

TSP, mg/filter

Quartz Filter Blank

TSP, mg/filterPM10, mg/filter

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Table 10: PM2.5 in AirFebruary 2003

Mugah Creek Remediation ProgramSydney, Nova Scotia

Henry Street Kings Road Intercolonial Street Kings Road Field Blank Henry Street Kings Road Intercolonial Street

1111-25-33-L3-080203-AC-6520

1112-25-33-L4-080203-AC-6521

1113-25-33-L5-080203-AC-6542

1114-25-33-L4-080203-AC-6543A

1136-25-33-L3-200203-AC-6522

1137-25-33-L4-200203-AC-6523

1138-25-33-L5-200203-AC-6524

µg µg µg µg µg µg µg277 117 118 8 217 171 191

µg/m3 µg/m3 µg/m3 µg/m3 µg/m3 µg/m3

11.55 4.87 4.91 NA 9.04 7.16 7.95NA = Not applicable

February 20, 2003February 8, 2003

PM2.5

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APPENDIX C

Environment Canada VOC Duplicate Results

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February 20, 2003 Collocated Samples Field Sample ID Canister ID 1118-V-33-L5-200203-AC-M31 KC-M31 1121-V-33-L5-200203-AC-M39B KC-M39 All values in µg / m3 28-Jan-03

MDL Method Blank KC-M31 KC-M39

Freon 12 (Dichlorodifluoromethane) 0.018 0.014 2.54 2.95 Chloromethane 0.018 0.010 1.16 1.12 Freon 114 (1,2-Dichlorotetrafluoroethane) 0.027 0.025 0.09 0.10 Vinylchloride (Chloroethene) 0.006 < 0.01 0.01 Bromomethane 0.021 < 0.06 0.05 Chloroethane 0.013 < 0.10 0.05 Freon 11 (Trichlorofluoromethane) 0.006 < 1.38 1.46 1,1-Dichloroethene 0.013 < 0.01 0.01 Dichloromethane 0.013 0.019 7.27 8.92 Freon 113 (1,1,2-Trichlorotrifluoroethane) 0.011 < 0.51 0.52 1,1-Dichloroethane 0.009 < < < c-1,2-Dichloroethene 0.009 < < < Chloroform 0.006 < 0.15 0.23 1,2-Dichloroethane 0.011 < 0.04 0.04 1,1,1-Trichloroethane 0.007 < 3.25 2.09 Benzene 0.013 0.009 1.98 1.33 Carbontetrachloride 0.014 < 0.50 0.46 1,2-Dichloropropane 0.009 < 0.01 0.01 Trichloroethylene 0.012 0.009 2.03 1.61 c-1,3-Dichloropropene 0.003 < < < t-1,3-Dichloropropene 0.006 < < < 1,1,2-Trichloroethane 0.015 < < < Toluene 0.013 < 3.36 4.52 1,2-Dibromoethane 0.027 < < < Tetrachloroethene 0.016 < 0.11 0.14 Chlorobenzene 0.009 < 0.02 0.01 Ethylbenzene 0.007 < 0.36 0.45 m,p-Xylene 0.012 < 1.03 1.26 Styrene 0.003 0.004 0.07 0.19 1,1,2,2-Tetrachloroethane 0.017 < < < o-Xylene 0.007 < 0.39 0.45 1,3,5-Trimethylbenzene 0.004 < 0.20 0.18 1,2,4-Trimethylbenzene 0.008 < 0.71 0.63 Benzyl Chloride 0.009 < < < 1,3-Dichlorobenzene 0.015 < < < 1,4-Dichlorobenzene 0.007 < 0.04 0.07 1,2-Dichlorobenzene 0.014 < < < 1,2,4-Trichlorobenzene 0.025 < < < Hexachlorobutadiene 0.035 < < <

Sample date 20-Feb-03 20-Feb-03 Date of Receipt 07-Mar-03 07-Mar-03 Analysis Date 07-Mar-03 07-Mar-03 07-Mar-03 Initial Pressure / Vacuum 2.1 psig 3.7 psig Valve Type PGI PGI Lab File Name BL096C.D SYD031.D SYD032.D

note : no "correction" of sample data for negligible VOC levels in method blank < = Less Than Method Detection Limit