Monthly and annual site performance and explanations are shown in table 3, based on 10–minute averages for continuously monitored data. Per cent of valid data (V) is defined as the per cent of valid data following quality assurance adjustments. Per cent of captured data (C) is the per cent of valid data excluding calibration and maintenance.
The 2000 Ministry for the Environment Good Practice Guide for Air Quality Monitoring and Data Management suggests that it is difficult to reach anything close to 100 per cent valid data for long-term monitoring. As such, site performance has been evaluated against a target of 95 per cent for capture data and 75 per cent for valid data.
The performance of continuously monitored pollutant instruments during 2009 was generally very good. All sites had annual valid data and data capture rates greater than 95 per cent with the exception of TSP at St Albans.
Table 3: Percentage valid and capture data, 2009
CO was monitored at Greers Road, Burnside. One-hour and eight-hour rolling averages have been calculated from 10-minute averages recorded by the instrument.
Summary statistics for CO and their dates are described below.
| Site | Maximum 1-hour average (mg/m3 ) | 99.9 percentile 1-hour average (mg/m3 ) | Maximum 8-hour average (mg/m3 ) | 99.9 percentile 8-hour average (mg/m3 ) |
|---|---|---|---|---|
| Greers Road, Burnside |
11.5 (26 June 22:00) |
7.7 |
7.6 (27 June 01:00) |
6.6 |
At Greers Road, Burnside during 2009 there were no exceedences of the ambient air quality one-hour guideline (30 mg/m3) or the eight-hour national environmental standard (10 mg/m3). Carbon monoxide results are shown in figures 7 to 11.
Oxides of nitrogen were monitored at Gavin Street, Penrose and Greers Road, Burnside. One hour and 24-hour averages have been calculated from 10-minute averages recorded by the instruments.
Summary statistics for NO2 and their dates for each site are described below.
| Site | Maximum 1-hour average (µg/m3 ) | 99.9 percentile 1-hour average (µg/m3 ) | Maximum 24-hour average (µg/m3 ) | 99.5 percentile 24-hour average (µg/m3 ) |
|---|---|---|---|---|
| Gavin Street, Penrose |
221.3 (5 April 13:00) |
137.0 |
54.1 (5 April) |
53.2 |
| Greers Road, Burnside |
67.4 (5 June 11:00) |
57.6 |
34.5 (9 September) |
31.8 |
At Gavin Street, Penrose, there was one exceedence of the NO2 one-hour national environmental standard (200 µg/m3) and no exceedences of the NO2 24-hour guideline (100 µg/m3). The 2009 NOx results for Penrose are shown in figures 12 to 21.
The 1-hour NO2 national environmental standard exceedence of 221.3μg/m³ was on 5 April 2009 at 13:00. The source of this exceedence was most likely from construction work. A crane was being used to move transformers 5–10 m from the Penrose monitoring site operating from 1 April to 6 April 2009. Elevated levels of NO2 occurred throughout this period due to the construction work.
There were no exceedences of the NO2 one-hour national environmental standard (200 µg/m3) or the NO2 24-hour guideline (100 µg/m3) in Christchurch during the 12-month period. The 2009 NOx results for Burnside are shown in figures 22 to 31.
Sulphur dioxide was monitored at Gavin Street, Penrose and Greers Road, Burnside. One-hour and 24-hour averages have been calculated from 10-minute averages recorded by the instruments.
Summary statistics for SO2 and their dates for each site are described below.
| Site | Maximum 1-hour average (µg/m3 ) | 99.9 percentile 1-hour average (µg/m3 ) | Maximum 24-hour average (µg/m3 ) | 99.5 percentile 24-hour average (µg/m3 ) |
|---|---|---|---|---|
| Gavin Street, Penrose |
51.6 (13 July 08:00) |
27.3 |
13.0 (12 July) |
11.4 |
| Greers Road, Burnside |
111.8 (20 March 01:00) |
49.3 |
22.9 (16 March) |
19.1 |
There were no exceedences of the SO2 national environmental 1-hour standard (350 µg/m3) or the 24-hour guideline (120 µg/m3) during 2009 at any site. The 2009 SO2 results for Gavin Street, Penrose are shown in figures 32 to 36 and Greers Road, Burnside are shown in figures 37 to 41.
Monitoring of VOCs was conducted at three sites: Gavin Street, Penrose; Greers Road, Burnside; and Coles Place, Christchurch. VOC monitoring utilises passive sampling badges exposed over a three-month period. Results for each 2009 quarter are shown in tables 4 to 7.
The benzene guideline is 10 µg/m3 as an annual average, with an average value of 3.6 µg/m3 to be achieved by 2010. The 2009 six-month and 12-month averages are described below. The benzene annual averages from all the sites are less than the annual average guideline (10 µg/m3) and are graphed in figure 1.
| Site |
Six-month average (January–June 2009) benzene (µg/m3 ) |
Six-month average (July–December 2009) benzene (µg/m3 ) |
2009 annual average benzene (µg/m3 ) |
|---|---|---|---|
| Gavin Street, Penrose | 0.9 | 0.7 | 0.8 |
| Greers Road, Burnside | 1.0 | 1.0 | 1.0 |
| Coles Place, St Albans | 1.1 | 1.0 | 1.0 |
| January–February–March 2009 | Limit of detection (µg/m3) |
Results (µg/m3) | ||
|---|---|---|---|---|
| Analyte | Coles Place | Burnside | Penrose | |
| Target VOCs | ||||
| ethanol | ND | |||
| isopropyl alcohol | ND | |||
| acetone | ND | |||
| pentane | ND | |||
| dichloromethane | ND | |||
| butan-2-one | ND | |||
| hexane | 0.5 | 0.7 | 1.1 | 0.9 |
| ethyl acetate | ND | |||
| trichloromethane | ND | |||
| 1,1,1-trichloroethane | ND | |||
| n-butanol | ND | |||
| benzene | 0.3 | 0.6 | 0.5 | 0.8 |
| 2-methylhexane | ND | |||
| 2,3-dimethylpentane | ND | |||
| 3-methylhexane | ND | |||
| heptane | 0.6 | 0.9 | ||
| trichloroethene | ND | |||
| propyl acetate | ND | |||
| methylcyclohexane | ND | |||
| 4-methylpentan-2-one | ND | |||
| toluene | 0.3 | 3.3 | 3.3 | 5.4 |
| octane | ND | |||
| tetrachloroethene | ND | |||
| butyl acetate | ND | |||
| ethylbenzene | 0.3 | 0.6 | 0.5 | 0.9 |
| m+p-xylene | 0.3 | 1.3 | 1.2 | 2.7 |
| styrene | ND | |||
| o-xylene | 0.3 | 0.5 | 0.5 | 0.9 |
| nonane | ND | |||
| alpha pinene | ND | |||
| propylbenzene | ND | |||
| 1,3,5-trimethylbenzene | ND | |||
| beta pinene | ND | |||
| decane | ND | |||
| 1,2,4-trimethylbenzene | 0.7 | 0.7 | 1.1 | |
| limonene | ND | |||
| undecane | ND | |||
| dodecane | ND | |||
| tetradecane | ND | |||
ND = Not detected.
| April–May–June 2009 | Limit of detection (µg/m3) | Results (µg/m3) | ||
|---|---|---|---|---|
| Analyte | Coles Place | Burnside | Penrose | |
| Target VOCs | ||||
| ethanol | ND | |||
| isopropyl alcohol | ND | |||
| acetone | ND | |||
| pentane | 2.3 | 4.5 | 3.8 | 11.3 |
| dichloromethane | ND | |||
| butan-2-one | ND | |||
| hexane | 0.5 | 0.8 | 0.9 | 1.1 |
| ethyl acetate | ND | |||
| trichloromethane | ND | |||
| 1,1,1-trichloroethane | ND | |||
| n-butanol | ND | |||
| benzene | 0.2 | 1.6 | 1.5 | 1.0 |
| 2-methylhexane | ND | |||
| 2,3-dimethylpentane | ND | |||
| 3-methylhexane | 0.5 | 0.6 | ||
| heptane | ND | |||
| trichloroethene | ND | |||
| propyl acetate | ND | |||
| methylcyclohexane | ND | |||
| 4-methylpentan-2-one | ND | |||
| toluene | 0.3 | 4.1 | 3.6 | 5.8 |
| octane | ND | |||
| tetrachloroethene | ND | |||
| butyl acetate | ND | |||
| ethylbenzene | 0.3 | 0.6 | 0.5 | 0.8 |
| m+p-xylene | 0.3 | 1.9 | 1.6 | 3.0 |
| styrene | ND | |||
| o-xylene | 0.3 | 0.7 | 0.6 | 1.0 |
| nonane | ND | |||
| alpha pinene | ND | |||
| propylbenzene | ND | |||
| 1,3,5-trimethylbenzene | ND | |||
| beta pinene | ND | |||
| decane | ND | |||
| 1,2,4-trimethylbenzene | 0.6 | 1.0 | 0.8 | 0.8 |
| limonene | ND | |||
| undecane | ND | |||
| dodecane | ND | |||
| tetradecane | ND | |||
ND = Not detected.
| July–August–September 2009 | Limit of detection (µg/m3) |
Results (µg/m3) | ||
|---|---|---|---|---|
| Analyte | Coles Place | Burnside | Penrose | |
| Target VOCs | ||||
| ethanol | ND | |||
| isopropyl alcohol | ND | |||
| acetone | ND | |||
| pentane | 2.3 | 3.4 | 3.4 | 7.5 |
| dichloromethane | ND | |||
| butan-2-one | ND | |||
| hexane | 0.5 | 1.0 | 1.3 | 0.9 |
| ethyl acetate | ND | |||
| trichloromethane | ND | |||
| 1,1,1-trichloroethane | ND | |||
| n-butanol | ND | |||
| benzene | 0.2 | 1.5 | 1.5 | 0.9 |
| 2-methylhexane | ND | |||
| 2,3-dimethylpentane | ND | |||
| 3-methylhexane | 0.5 | 0.6 | ||
| heptane | 0.5 | 0.7 | 0.5 | |
| trichloroethene | ND | |||
| propyl acetate | ND | |||
| methylcyclohexane | ND | |||
| 4-methylpentan-2-one | ND | |||
| toluene | 0.3 | 4.8 | 4.0 | 4.7 |
| octane | ND | |||
| tetrachloroethene | ND | |||
| butyl acetate | ND | |||
| ethylbenzene | 0.3 | 0.7 | 0.6 | 0.6 |
| m+p-xylene | 0.3 | 2.2 | 1.8 | 2.2 |
| styrene | ND | |||
| o-xylene | 0.3 | 0.7 | 0.6 | 0.7 |
| nonane | ND | |||
| alpha pinene | ND | |||
| propylbenzene | ND | |||
| 1,3,5-trimethylbenzene | ND | |||
| beta pinene | ND | |||
| decane | ND | |||
| 1,2,4-trimethylbenzene | 0.6 | 0.8 | 0.6 | 0.7 |
| limonene | ND | |||
| undecane | ND | |||
| dodecane | ND | |||
| tetradecane | ND | |||
ND = Not detected.
October–November–December 2009 |
Limit of detection |
Results (µg/m3) |
||
|---|---|---|---|---|
Analyte |
Coles Place |
Burnside |
Penrose |
|
Target VOCs |
|
|
|
|
ethanol |
ND |
|
|
|
isopropyl alcohol |
ND |
|
|
|
acetone |
ND |
|
|
|
pentane |
2.1 |
|
|
4.7 |
dichloromethane |
ND |
|
|
|
butan-2-one |
ND |
|
|
|
hexane |
0.4 |
0.4 |
1.0 |
0.6 |
ethyl acetate |
ND |
|
|
|
trichloromethane |
ND |
|
|
|
1,1,1-trichloroethane |
ND |
|
|
|
n-butanol |
ND |
|
|
|
benzene |
0.2 |
0.5 |
0.4 |
0.6 |
2-methylhexane |
ND |
|
|
|
2,3-dimethylpentane |
ND |
|
|
|
3-methylhexane |
0.5 |
|
0.5 |
|
heptane |
0.5 |
|
0.7 |
|
trichloroethene |
ND |
|
|
|
propyl acetate |
ND |
|
|
|
methylcyclohexane |
ND |
|
|
|
4-methylpentan-2-one |
ND |
|
|
|
toluene |
0.2 |
1.8 |
1.9 |
3.3 |
octane |
ND |
|
|
|
tetrachloroethene |
ND |
|
|
|
butyl acetate |
ND |
|
|
|
ethylbenzene |
0.3 |
0.3 |
0.3 |
0.6 |
m+p-xylene |
0.3 |
1.0 |
0.9 |
1.7 |
styrene |
ND |
|
|
|
o-xylene |
0.3 |
0.4 |
0.3 |
0.6 |
nonane |
ND |
|
|
|
alpha pinene |
ND |
|
|
|
propylbenzene |
ND |
|
|
|
1,3,5-trimethylbenzene |
ND |
|
|
|
beta pinene |
ND |
|
|
|
decane |
ND |
|
|
|
1,2,4-trimethylbenzene |
0.6 |
|
0.6 |
0.7 |
limonene |
ND |
|
|
|
undecane |
ND |
|
|
|
dodecane |
ND |
|
|
|
tetradecane |
ND |
|
|
|
ND = Not detected.

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In 2009, all annual average benzene results at all sites were within the current ambient air quality guideline of 3.6 mg/m3.
PM10 was monitored at Gavin Street, Penrose and Greers Road, Burnside. Twenty-four-hour averages have been calculated from 10-minute averages recorded by the instruments.
Summary statistics for PM10 and their dates for each site are described below.
| Site | Maximum 24-hour average (µg/m 3 ) | 99.5 percentile 24-hour average (µg/m 3 ) |
|---|---|---|
| Gavin Street, Penrose |
132 (25 September) |
40 |
| Greers Road, Burnside |
108 (4 June) |
70 |
There was one exceedence of the 24-hour national environmental standard (50 µg/m3) at the Auckland site during 2009. This PM10 exceedence of 132 μg/m³ occurred on 25 September 2009 and is the highest ever recorded at the Penrose site. Elevated levels of PM10 were recorded at Penrose from 24 September at 21:10 until 25 September at 10:50. Particulate matter collected during this period was orange and originated from Australian dust storms. The 2009 PM10 results for Penrose are shown in figures 42 to 44.
At Greers Road, Burnside, there were nine exceedences of the 24-hour standard. Each exceedence and the date of the exceedence are listed in table 8 below. As there were multiple exceedences at the Christchurch site, more data analysis was carried out and reported in section 7.9. The 2009 PM10 results for Burnside are shown in figures 45 to 47.
Eight out of the nine exceedences occurred over the winter period, a time when wood burning is widely used for domestic heating. Cold winter conditions strongly influence air pollution in the region especially in calm conditions. The PM10 exceedence of 77 μg/m³ on 14 September 2009 was due to PM10 sources that originated from Australia. Elevated levels of PM10 were recorded at Burnside from 14 September at 09:20 until 15 September at 01:50.
| Date |
Burnside PM
10
( µ g/m 3 ) |
|---|---|
| 3 June 2009 | 57 |
| 4 June 2009 | 108 |
| 5 June 2009 | 63 |
| 26 June 2009 | 70 |
| 7 July 2009 | 51 |
| 9 July 2009 | 57 |
| 14 July 2009 | 57 |
| 26 July 2009 | 53 |
| 14 September 2009 | 77 |
Note: National environmental standard for PM10 = 50 µg/m³.
TSP is measured as a seven-day average at Gavin Street, Penrose and Coles Place, St Albans. Maximum results and their dates (seven-day ending period) for each site are described below.
| Site | Maximum seven-day average (µg/m 3 ) |
|---|---|
| Gavin Street, Penrose |
38 (30 September) |
| Coles Place, St Albans |
36 (2 July) |
There were no exceedences of the MoH guideline of 60 µg/m3 at any site. The TSP concentrations in Auckland are shown in figures 2 and 3 while Christchurch TSP concentrations are shown in figures 4 and 5.

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In 2009, all seven-day TSP results at the Penrose site were within the Ministry of Health guideline of 60 mg/m3. All seven day averages were below 30 mg/m3.

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The Penrose site has shown a downward trend over most of this period with a levelling off of values in recent years. TSP levels at this site have only exceeded the Ministry of Health guideline (60 mg/m3) in 1996 and 1999. TSP levels at the Kowhai and Kelly Street sites did not exceed the Ministry of Health guideline while they were operating.

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In 2009, TSP values remained below the Ministry of Health guideline throughout the year. Peak seven-day TSP levels occurred in June, July and August.

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Between 2002 and 2009, similar seasonal variations occurred each year, with peak levels occurring in or around June. A downward trend of peak levels occurred from 2005 to 2008. The peak TSP levels increased in 2009.
Lead is measured from seven-day averaged TSP samples to derive a three-month average at Gavin Street, Penrose and Coles Place, St Albans. The results are described in the table below. Figure 6 provides moving three-month averaged lead data between January 1996 and September 2000 when lead monitoring was performed on a monthly basis. From this point lead was monitored over a three-month period (June to August) annually.
| Site | June 2009 average (µg/m 3 ) | July 2009 average (µg/m 3 ) | August 2009 average (µg/m 3 ) | Winter 2009 average (µg/m 3 ) |
|---|---|---|---|---|
| Gavin Street, Penrose | 0.014 | 0.012 | 0.004 | 0.010 |
| Coles Place, St Albans | 0.025 | 0.029 | 0.031 | 0.028 |
No site exceeded the three-month average guideline for lead (0.2 µg/m3).

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Between 1996 and 2009, all lead results were within the ambient air quality guideline (0.2 mg/m3). The 3-month average levels in winter from 2003 to 2009 did not exceed 0.05 mg/m3.

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In 2009, all carbon monoxide results at the Burnside monitoring site were within the ambient air quality guideline (30 mg/m3). Peak levels occurred in June, July and August and were less than 15 mg/m3.

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Between 2003 and 2009, all carbon monoxide (CO) 1-hour average results were below the ambient air quality guideline (30 mg/m3). Annual variations in carbon monoxide levels were similar for all seven years, with peak levels generally occurring in June, July and August. The highest result was recorded in 2006 and was less than 15 mg/m3.

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In 2009, all carbon monoxide (CO) 8-hour average results were below the national environmental standard for CO (10 mg/m3). Peak levels occurred in June and July. Results were the lowest during the first and fourth quarters of the year.

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Between 2003 and 2009, the only exceedance of the national environmental standard for carbon monoxide (10 mg/m3) occurred in 2006. Peak levels halved in 2007, but have since steadily increased.

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Between 2003 and 2009, the highest carbon monoxide annual average was in 2006, while the lowest was in 2005. The annual average value has steadily decreased from 2006 to 2009.

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In April 2009, the national environmental standard for nitrogen dioxide (200 µg/m3) was exceeded. Nitrogen dioxide levels were below 100 mg/m3 in all other months.

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The national environmental standard for nitrogen dioxide was exceeded twice in the 13 years from 1997 to 2009, once in 2005 and once in 2009.

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In 2009, all nitrogen dioxide daily results at the Penrose site were within the ambient air quality guideline (100 µg/m3). There were no recorded results exceeding 60 µg/m3. Peak levels occurred between April and September.

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There have been no exceedances of the ambient air quality guideline (100 µg/m3) in the past 13 years. Nitrogen dioxide daily averages show similar annual trends from 1997 to 2009 with values increasing between April and September.

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There has been little change in annual nitrogen dioxide levels from 1997 to 2009. The highest annual average was in 2001 while the lowest was in 1998.

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In 2009, NO levels displayed a greater degree of variation throughout the year compared to NO2. Peak NO levels occurred in August, while peak NO2 levels occurred in April.

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In 2009, NO levels during most of the year were generally below 70 µg/m3 with peak levels occurring in June, July and August.

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Annual NO (1-hour average) trends are similar from 1997 to 2009 with peak levels generally occurring in June, July and /or August.

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Daily NO levels trends are similar from 1997 to 2009 with peak levels generally occurring in June, July and/or August.

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Annual averages of NO show a generally decreasing trend from 1997 to 2009. The annual NO level in 2009 is nearly half of the 1997 level.

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In 2009, all hourly NO2 results were below the national environmental standard (200 µg/m3). No result at the Burnside site was above 80 µg/m3. NO2 levels increased during the months of June to September.

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Between 2003 and 2009, no exceedances of the national environmental standard (200 µg/m3) occurred. All hourly NO2 results were less than 100 µg/m3. Levels increased during the months of June to September for all years.

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In 2009, the daily NO2 results were all within the ambient air quality guideline (100 µg/m3). All results were below 40 µg/m3. NO2 levels increased from June to September.

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Between 2003 and 2009, daily NO2 levels in the past six years were all below the ambient air quality guideline of (100 µg/m3). The highest daily NO2 average in Burnside occurred in the winter of 2005. Increased levels generally occurred during the months of May to September for all years.

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Between 2003 and 2009, the highest annual NO2 average occurred in 2005. The annual NO2 levels decreased from this peak in 2005.

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In 2009, hourly NO2 levels have less variation during the year than hourly NO levels. The hourly NO levels in Burnside peak in June and July, and are the lowest during the months of January and October-December.

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In 2009, the daily NO averages in Burnside have a great degree of variation during the year compared to NO2 daily averages. The peak levels occurred in June and July. Daily NO2 levels peaked in August and September.

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Annual NO (1-hour average) variations in Burnside were similar from 2003 to 2009 with peak levels occurring between June and September for all years. The highest result was recorded in 2006. The second highest hourly average was recorded in 2007 and the third highest in 2009.

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The variations in daily NO levels were similar from 2003 to 2009 with peak levels occurring between June and September for all years. The highest result was recorded in 2006. The second highest hourly average was recorded in 2009.

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The annual average NO level has increased from 2003, peaked in 2006 and has decreased since then.

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In 2009, there were no exceedances of the national environmental standards for SO2 (350 µg/m3). Hourly SO2 levels at Penrose were all below 50 µg/m3. Peak levels occurred in July and August.

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Between 2003 and 2009, there have been no exceedances of the national environmental standard for SO2 (350 µg/m3). For the past six years, the hourly SO2 levels at Penrose have been relatively similar. Peaks occurred in 2005 and 2009, but these were below 60 µg/m3.

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In 2009, all daily SO2 results at Penrose were below the ambient air quality guideline (120 µg/m3). Daily SO2 results from July and August were slightly higher than other months. Results from January to April and August to December were very low (less than 10 µg/m3).

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Between 2003 and 2009, the daily SO2 levels at the Penrose site were all below the ambient air quality guideline (120 µg/m3). The peak daily level was recorded in 2005. No daily result has been above 25 µg/m3 for the past seven years.

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The annual average SO2 at Penrose had an increasing trend from 2003, peaking in 2005, followed by a large decrease in annual SO2 levels in 2006. These levels decreased further in 2007 and again in 2008. Annual average levels increased in 2009.

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In 2009, all hourly SO2 results at Burnside were within the national environmental standard (350 µg/m3). There were elevated results in March but these were less than 120 µg/m3. Hourly SO2 results for the rest of the year were below 60 µg/m3.

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Between 2003 and 2009, there were no exceedances of the national environmental standard for SO2 (350 µg/m3). The highest hourly SO2 averages were recorded in 2003 and 2009. These were the only results that exceeded 100 µg/m3. Most of the hourly results for the other years were below 50 µg/m3.

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In 2009, all daily SO2 averages were below the ambient air quality guideline of 120 µg/m3. All results were below 30 µg/m3. Peak levels occurred in March and November.

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For the period 2003-2009, all daily levels of SO2 were below the ambient air quality guideline (120 µg/m3). Most of the daily SO2 results were below 20 µg/m3. Peak levels occurred in 2003 and 2006.

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There have been fluctuations in annual averages in the past six years. Results were similar from 2003 to 2005, they decreased in 2006 and 2007, and then increased in 2008 and 2009.

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In September 2009, one exceedance of the national environmental standard for PM10 (50 µg/m3) occurred. Generally daily PM10 levels were below 30 µg/m3. There were slightly elevated PM10 levels (but still below the standard) in March, June, August and December.

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All daily PM10 results from 2003 to 2008 were below the national environmental standard of 50 µg/m3. One exceedance occurred in 2009. PM10 levels varied within each year.

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All annual average PM10 levels from 2003 to 2009 were below the ambient air quality guideline of 20 µg/m3. The lowest annual average at Penrose was recorded in 2005 while the highest was in 2003.

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In 2009, there were 9 exceedances of the national environmental standard (50 µg/m3) for daily PM10. The exceedances ranged from 51 to 108 µg/m3 and occurred in June, July and September.

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There have been yearly exceedances of the national environmental standard for PM10 (50 µg/m3) between 2003 and 2009. The highest daily value was recorded in 2006. Peaks generally occurred during the months of June, July and August.

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Annual average PM10 levels in 2003 and 2004 were above the ambient air quality guideline of 20 µg/m3. Results from 2005 to 2009 were all below the guideline value with the lowest annual average recorded in 2007.
There was one NO2 national environmental standard exceedence at Penrose with the likely source being construction works near the monitoring station. There was also one PM10 standard exceedence at Penrose due to Australian dust. The nine PM10 exceedences recorded during 2009 at Greers Road, Burnside are examined below. All the other parameters monitored at all sites were below the National Environmental Standards (NES) for Air Quality.
The PM10 standard of 50 µg/m3 was exceeded on eight days in 2009 during the cooler months from June to July. During June there were three consecutive days that incurred exceedences (3–5 June). On 14 September there was one exceedence linked to Australian dust.
The typical diurnal trend in PM10 during winter is shown in figure 48. PM10 hourly averages for those days where the daily PM10 average exceeded 50 µg/m3 are plotted against time of day. From figure 48, the biggest contributions to PM10 levels were between the hours of 18:00 and 03:00. This would suggest contributions from wood burning for home heating. On 4 June PM10 concentrations remained high at night and in the morning. On 5 June elevated PM10 levels occur from the early morning until 11 am. On 14 September elevated PM10 levels start around 10am and remained throughout the day.
Figures 49, 50 and 51 plot PM10 hourly averages for those days where the daily PM10 average exceeded 50 µg/m3 against hourly average temperature measured at 1.5 m, and 10 m, and the difference between the two temperature heights. From figure 49, the biggest contributions to PM10 levels were when temperature measured at 1.5 m was below 5°C. Figure 50 shows the biggest contributions to PM10 levels were when temperature measured at 10 m was below 7°C. Figure 51 shows the biggest contributions to PM10 were when temperature difference between 10 m and 1.5 m was greater than zero, ie, when temperature inversion conditions prevailed. This is consistent with the trapping of pollutants and subsequent higher concentrations expected during temperature inversion conditions.
Figure 52 plots PM10 hourly averages for those days where the daily PM10 average exceeded 50 µg/m3 against hourly average relative humidity (RH). Figure 52 shows contribution to PM10 levels began when RH was above 75 per cent and peaked at around 95 per cent, ie, high RH conditions. This is consistent with diurnal RH patterns throughout the day.
Figure 53 plots PM10 hourly averages for those days where the daily PM10 average exceeded 50 µg/m3 against hourly average wind directions. Figure 53 shows no particular wind direction seems to contribute significantly higher concentrations of PM10 over other wind directions. This is consistent with an area with wide diffuse sources of pollution as opposed to point/line source of pollution. There were very few data points in the sector 120 degrees to 180 degrees as wind frequency from this sector is usually low.
Figure 54 plots PM10 hourly averages for those days where the daily PM10 average exceeded 50 µg/m3 against hourly average wind speeds. Figure 54 shows contributions to PM10 began when wind speed was below 1.5 m/s and peaked at a wind speed of 0.5 m/s, ie, low wind speed conditions. This is consistent with reduced dispersion under low wind speed conditions. On 5 June winds increased from mid-afternoon until the evening increasing dispersion and decreasing the PM10 concentrations.
Figure 55 plots PM10 hourly averages for those days where the daily PM10 average exceeded 50 µg/m3 against hourly average NO. Figure 55 shows a positive linear relationship seems to exist between PM10 and NO concentrations. This relationship is usually more defined at PM10 concentrations below 60 µg/m3 and NO concentrations below 80 µg/m3. This is expected as PM10 and NO is co-generated during the burning of wood and fossil fuels.
Figure 56 plots PM10 hourly averages for those days where the daily PM10 average exceeded 50 µg/m3 against hourly average CO. Figure 56 shows a positive linear relationship seems to exist between PM10 and CO concentrations. This relationship is usually more defined at PM10 concentrations below 60 µg/m3 and CO concentrations below 2.5 mg/m3. This is expected as PM10 and CO is co-generated during the burning of wood and fossil fuels.
Figure 57 plots PM10 hourly averages for those days where the daily PM10 average exceeded 50 µg/m3 against hourly average SO2. Figure 57 shows the relationship between PM10 and SO2 concentrations seems to depend on the exceedence day. On a few days there seems to be a positive trend although this is probably due to meteorological conditions.
From the comparisons of available meteorological parameters and other pollutants as discussed above, it can be concluded that almost all of the PM10 exceedences were likely due to home heating during the colder months. This is observed especially in the evenings, when PM10 levels are worsened by temperature inversions trapping the pollutants and low wind speed conditions preventing effective dispersion of pollutants.
The elevated PM10 concentrations on 14 September are the exception as the source was linked to Australian dust. The elevated levels occurred from 09:20 onward. With PM10 concentrations greater than 50 µg/m³ the meteorological conditions for the day were warm and dry with low to gentle breezes.

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In 2009, the biggest contributions to PM10 in 2009 were between the hours of 18:00 and 03:00 peaking at around 22:00.

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In 2009, the biggest contributions to PM10 when the temperature, measured at 1.5 m, was below 5 °C.

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In 2009, the biggest contributions to PM10 were when the temperature, measured at 10 m, was below 7°C.

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In 2009, the biggest contributions to PM10 were when the temperature difference between 10 and 1.5 metres was greater than zero. This is when temperature inversion conditions occur.

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In 2009, PM10 began increasing when the relative humidity was above 75 per cent and peaked at around 95 per cent.

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In 2009, no wind direction seemed to contribute significantly higher PM10 levels than any other wind direction. There were very few data points from 120 to 180 degrees as wind frequency from this sector is usually low.

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In 2009, the biggest contributions to PM10 began when wind speed was below 1.25 m/s and peaked at a wind speed of 0.25 m/s.

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In 2009, a positive linear relationship seemed to exist between PM10 and NO levels. This relationship is more defined at PM10 levels below 60 µg/m3 and NO levels below 80µg/m3.

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In 2009, a positive linear relationship seemed to exist between PM10 and CO levels. This relationship is more defined at PM10 levels below 60 µg/m3 and CO levels below 2.5 mg/m3.

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In 2009, a relationship between PM10 and SO2 concentrations seemed to depend on the day of the exceedence. On a few days there seemed to be a positive trend although this is probably due to meteorological conditions.