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Original article

Human health risks posed by exposure to PM10 for four life stages in a low socio-economic community in South Africa

Human health risks posed by exposure to PM10 for four life stages in a low socio-economic community in South Africa

 

Nomsa Duduzile Lina Thabethe1, Jacobus Christoffel Engelbrecht1,&, Caradee Yael Wright2, Maria Aletta Oosthuizen2

 

1Tshwane University of Technology, Faculty of Science, Department of Environmental Health, Private Bag X680, Pretoria. 0001. South Africa, 2Council for Scientific and Industrial Research, Climate Studies, Modelling and Environmental Health, P.O Box 395, Pretoria, 0001. South Africa

 

 

&Corresponding author
Jacobus Christoffel. Engelbrecht, Tshwane University of Technology, Faculty of Science, Department of Environmental Health, Private Bag X680, Pretoria. 0001, South Africa

 

 

Abstract

Introduction: Mine ash dumps, industries and domestic fuel use have a great impact on air quality and PM10 (particles with a diameter equal to or less than 10 µm) is a pollutant of particular concern.

 

Methods: The objective of this study was to assess the human health risks posed by exposure to PM10 among a low socio-economic community. The Human Health Risk Assessment (HHRA) framework (i.e. hazard assessment, dose-response assessment, exposure assessment and risk characterization) was applied. PM10 concentrations were monitored for one month during winter and summer, respectively. A HHRA was conducted to assess whether the community was exposed to PM10 concentrations that may pose carcinogenic and non-carcinogenic health risks.

 

Results: Generally, the residents were exposed to higher concentrations of PM10 during winter than summer, resulting in a higher risk to health during winter. Results of the HHRA showed that infants were exposed to a higher dose of PM10 than the other life stages when exposed to the same concentration due to differences in inhalation rates and the ratio between inhalation and body weight. However, they were at the same risk of developing adverse effects from exposure to the same concentration of PM10 as the other life stages were exposed to, because the 'safe' dose was also higher for infants and since all life stages, in general, are similarly affected by PM unless the chemical composition of the PM is known.

 

Conclusion: This study recommends that infants and children, in particular, should not be exposed to air pollution from domestic fuel burning as one positive step to try and reduce their dose.

 

 

Introduction

Particulate matter (PM) is a complex, heterogeneous mixture of smoke, soot, dust, salt, acids, and metals and varies in concentration, size, chemical composition, surface area and sources of origin [1]. PM may comprise, among others, sulphate, nitrate, ammonia, chloride and organic carbon particles [2]. PM10 is defined as particles with a diameter of equal to or less than 10 microns. Exposure to 10 in particular, poses a definite risk to health because it is more likely to be inhaled and the fine fraction of PM10 (i.e. PM2.5) is respirable and may reach the alveolar region of the lung. Ultra-fine PM (i.e. PM0.1) that is inhaled settles in the lung by Brownian motion and some may be exhaled before it deposits in the lungs [3].

 

One area that is surrounded by industries, power stations and mines, all of which are recognised emitters of PM, is that of eMbalenhle, a township located in the Mpumalanga Province of South Africa, about 12 km from the town of Secunda . Domestic fuel burning has a great impact on air quality in eMbalenhle. The major sources of PM in eMbalenhle are motor vehicles, domestic fuel burning, mine ash dumps, dust from unpaved roads, landfills, agriculture, wildfires, waste burning, industrial sources and windblown dust from open lands. Given these air pollution sources, it was deemed necessary to estimate the likely human health risks posed by PM10 to the residents of eMbalenhle, an activity never done before for this geographic region, for future planning and management of air pollution in the area.

 

 

Methods

The study comprised two parts namely an ambient air quality monitoring and a Human Health Risk Assessment (HHRA).

 

Ambient air quality monitoring

 

A TOPAS airborne particulate monitor (Sira MC 090158/00) was used to measure the ambient PM10 concentrations to which the population of eMbalenhle were exposed. The monitor was installed at eMbalenhle Sasol Club, alongside the Department of Environmental Affairs (DEA) monitoring station (GPS coordinates: S26°33,039' and E29°04,747'). Ambient PM10 concentrations were monitored for one month during winter (August 2010) and one month during summer (February 2011). DEA monitoring station data were also extracted for the same periods as the TOPAS instrument was installed for comparison purposes.

 

The particulate monitor was calibrated and maintained according to the manufacturers specifications. The fibre filters were replaced once after two weeks. Monitored data used to assess the health risks posed by exposure to PM10 in the population of eMbalenhle were compared with the South African National Ambient Air Quality Standard (NAAQS) [4]. The PM10 concentrations were measured in 15 minutes intervals, the raw data output was divided by a calibration factor of 2 and the 24-hour averages were calculated. The monitored PM10 concentrations were compared with the NAAQS which were originally set to protect human health.

 

Human Health Risk Assessment

 

HHRA is a useful tool to estimate human health risks posed by exposure to a given environmental pollutant. HHRA have been applied in previous studies in South Africa, for example to estimate kerosene [5] and sulphur dioxide-related health risks [6]. However, a HHRA on PM10 has never been conducted in eMbalenhle. The HHRA framework applied in this study comprised four parts: hazard identification, exposure assessment, dose-response assessment and risk characterisation. The formal identification of PM10 as a hazard as well as the types of health risks that may occur as a result of exposure to PM10 was done from existing literature.

 

Dose-response assessment, i.e. how an individual will react to a particular exposure, was not performed in this study as the extent of the work requires comprehensive screening and additional health data presently not available in South Africa. Instead, the measured levels of PM10 were compared with the NAAQS. This national standard was therefore used as a benchmark value.

 

The information obtained during the hazard identification and the exposure assessment was used to estimate the concentrations of PM10 that are likely to cause significant health risks in humans. The PM10 monitored data were used to estimate how the different levels of exposure to PM10 can impact on the likelihood and severity of health effects.

 

It was postulated that the population of eMbalenhle was exposed to levels exceeding the NAAQS for PM10 that may have a negative impact on their health. It was assumed that inhalation was the most important route of exposure (not ingestion or dermal contact) and that people were exposed for 24 hours per day.

 

Two equations were used to characterise the risks posed by exposure to PM10, namely; the United States Environmental Protection Agency (USEPA) Exposure Factors Handbook and the EPA Integrated Risk Information System (IRIS) equations [7]. The magnitude, frequency and duration of exposure of the population of eMbalenhle to PM10 were unknown, thus the default values based on the USEPA equations were used. The South African 24-hour PM10 NAAQS of 120 µg/m3 was used as a benchmark value.

 

The USEPA equation was used to calculate the Field Average Daily Dose (FADD). In order to calculate the FADD, the average concentrations (C) of P PM10 monitored in eMbalenhle in August 2010 and February 2011 were multiplied by the Inhalation Rate (IR), Exposure Frequency (EF) and Exposure Duration (ED), and then divided by the Body Weight (BW) multiplied by the Average Time (AT).

 

FADD was calculated using the following equation:

 

FADD = C × IR × EF x ED/ BW × AT (Equation 1)

 

Where:

 

FADD is the dose the population of eMbalenhle may be exposed to when inhaling PM10 concentrations measured at eMbalenhle in August 2010 and February 2011, expressed in µg/kg/day.

 

C is the average value of the PM10 concentration in the atmosphere expressed in µg/m3. IR is the amount of contaminated medium (air) inhaled per unit time or event. It is expressed in m3/day.

 

EF (Exposure Frequency) which is 350 days, because it was assumed that a person will leave the area for about two weeks per year.

 

ED (Exposure Duration) expressed in years. For non-carcinogens assumed to be one year. BW is the average body weight of the receptor over the exposure period (kg). AT is the period over which exposure is averaged (1 year = 365 days). For non- carcinogens the AT equals ED (years) multiplied by 365 days [7].

 

The long-term inhalation rates for adults and children (including infants) were presented as daily rates (m3/day). It was assumed that the 95th percentile inhalation rates for long-term exposures for infants, children and adults (males and females combined, unadjusted for body weight) range from 9.2 m3/day for infants from birth to 1 year, 16.6 m3/day for children aged 6 to 10 years to 21.4 m3/day for adults aged 31 to 40 years [7].

 

The Safe Average Daily Dose (SADD) was calculated as follows:

 

SADD = C × IR × ED/ BW × AT (Equation 2)

 

Where:

 

SADD is the dose that the population of eMbalenhle may be exposed to without suffering negative health risks, expressed in µg/kg/day. In this case the concentration C represents the South African 24-h standard for PM10 expressed in µg/m3. The rest of the formula is the same as described above.

 

The risks caused by exposure to PM10 in the population of eMbalenhle were characterised in terms of the potential risk to illness or symptoms in the exposed population. The information developed in the previous three steps (hazard identification, exposure assessment and dose-response assessment) was brought together in the risk characterisation step to quantify the potential health risks in the exposed population, expressed as a Hazard Quotient (HQ).

 

The HQ was calculated using the following equation [7]:

 

HQ = FADD / SADD (Equation 3)

 

Where:

 

HQ is the Hazard Quotient (which is always unit less)

 

FADD is the Field Average Daily Dose calculated (in µg/kg/day)

 

SADD is the "safe" average daily dose calculated (in µg/kg/day)

 

Guidelines for interpreting HQ calculations are (Lemly, 1996):

 

HQ <0.1: no hazard exists;

 

HQ 0.1-1.0: the hazard is low;

 

HQ 1.1-10: the hazard is moderate; and

 

HQ >10: hazard is high

 

All statistical analyses were performed in Microsoft Excel. Ethical clearance was obtained for this study from the Tshwane University of Technology Research Ethics Committee on the 14th March 2011 (Reference number: 2011/03/007).

 

 

Results

Measured results of PM10

 

The measured 24-hour average PM10 concentrations for winter (August 2010) and summer (February 2011) using both the TOPAS and DEA instruments are presented in Figure 1 and Figure 2, respectively. The PM10 concentrations measured in August 2010 were generally higher than the PM10 concentrations measured in February 2011. The 24-h average level for PM10 (August 2010) was 157.37 µg/m3 and the 24-h average NAAQS of 120 µg/m3 was exceeded on most of the days.

 

Figure 2 illustrates the PM10 concentrations monitored with the TOPAS and DEA instruments during February 2011. The particle pollution reported was relatively low (24-h average 63.70 µg/m3), which means that even if the population of eMbalenhle was exposed to that average concentration of PM10, negative health impacts would be unlikely, as concentrations were below the 24-hour average NAAQS of 120 µg/m3, although some individuals may still be sensitive to relatively low PM10 concentrations [8].

 

Figure 3 presents the concentrations of PM10 versus time of the day. High concentrations of PM10 were reported in eMbalenhle between 04:45 and 07:45 probably due to the fact that people were burning domestic fuel to prepare for work and they also travelled from different areas during these times, thus elevated vehicle emission levels were present. Figure 3 reflects that between 9:45 and 16:45, the PM10 concentrations decreased because most residents were at work, thus the need for energy for cooking and space heating decreased. Between 17:45 and 21:45, the PM10 concentrations increased because residents were home and engaged in cooking and household activities requiring domestic fuel use.

 

A comparison between the winter and summer data from the TOPAS PM10 data and DEA PM10 data was made (Figure 4 and Figure 5 respectively). Although the monitoring equipment were placed at the same site, monitoring the same pollutant (PM10) and within the same period (August 2010 and February 2011), the PM10 concentrations monitored with the TOPAS monitor were higher (but following a similar pattern in most cases) than those monitored by the DEA monitoring station. The reason could be that an error occurred during sampling or that one of the instruments was not calibrated appropriately. Generally, when the PM10 concentrations monitored with the TOPAS monitor increased, the PM10 concentrations monitored by DEA monitoring station also increased and vice-versa. However, the DEA PM10 instrument measured on average three times lower than the TOPAS instrument. Hence, to determine the worst-case scenario risk estimates, the TOPAS data were used for the HHRA.

 

Human health risk assessment in eMbalenhle

 

The PM10 concentrations monitored in eMbalenhle in August 2010 and February 2011 were applied in the USEPA HHRA model to assess and characterise the potential health risks posed by the community. The population of eMbalenhle was categorised into three life-stage scenarios (infant, child and adult). The three life-stage scenarios were categorised based on the fact that infants, children and adults are exposed differently to PM10.

 

As per the USEPA Exposure Factors Handbook [7], the identified life-stage scenarios have 95th percentile inhalation rates of 7.1 m3/day, 16.6 m3/day and 21.4 m3/day for an infant (birth to 1 year), a child (6 to 11 years) and an adult (31 to 41 years) respectively. It was assumed that the BW of an infant is 9.2kg, that of a child 52.5kg and that of an adult 118kg [7] .

 

Table 1 gives the SADD of the three life-stage scenarios. The SADD was calculated using equation 2 (multiplying the "safe" PM10 concentration (C) of 120 µg/m3 with the Inhalation Rate (IR), the Exposure Frequency (EF) and the Exposure Duration (ED), then divided by the Body Weight (BW) multiplied by the Average Time (AT).

 

The FADD was calculated using Equation 1 (multiplying the measured PM10 concentrations monitored in winter and summer by the IR, the EF and the ED, divided by the BW multiplied by the AT). The results of the FADD for the PM10 concentrations measured in winter for the different life-stages are given in Table 2.

 

The results of the FADD for the PM10 concentrations measured in summer for the different life-stages are given in Table 3. For each life-stage, the winter dose was higher than the summer dose.

 

In order to characterise the health risks posed by exposure to PM10 in the different life-stage scenarios, the Hazard Quotient (HQ) was calculated by dividing the calculated FADD by the calculated SADD.

 

Another method of calculating an HQ to characterise the risk, is to directly divide the actual level of exposure (the concentration measured in the field), by the level of exposure that is not expected to cause adverse effects (the bench mark concentration, which in this case was the national 24-h standard for PM10). This method can only be used in the case of inhalation, where both the level of exposure and the benchmark value are presented as a concentration (mass per volume), to have a unit less HQ. The results of the HQ calculations are presented in Table 4 and Table 5. In winter (August 2010), the HQ was 2.97, indicating a moderate risk according to [9] and in summer (February 2011) the HQ was 0.53, indicating that adverse health effects were unlikely, thus a low risk.

 

The calculated HQs using the IRIS formula, of dividing the concentration by a benchmark concentration, were between 1.1 and 10 for the winter period, which means that the population of eMbalenhle were at moderate risk of negative health effects from exposure to PM10. In summer, the HQs were above 0.1 but below 1, which means that the population of eMbalenhle were at low risk and it is unlikely that they may have experienced negative health effects due to PM10 exposure.

 

 

Discussion

This study aimed to determine the human health risks posed by ambient PM10 concentrations to residents of eMbalenhle in an air pollution hotspot area in South Africa. Similar studies have been carried out elsewhere in the world [10-11]. Our results showed that ambient PM10 concentrations were higher during the winter month than the summer month. Possible reasons for the elevated levels in winter may be adverse climatic conditions (such as inversion layers), increased domestic coal burning for space heating, as well as wind-blown dust from mine ash dumps and unpaved roads during the windy month of August. In summer, PM10 concentrations were lower, despite industrial emissions that probably remained constant throughout the year, likely due to rain that washed the particulates out of the atmosphere and a decrease in domestic fuel burning due to warmer ambient temperatures as well as less wind-blown dust and the absence of inversion layers.

 

The PM10 concentrations monitored in winter exceeded the national 24-hr average standard of 120 µg/m3 on at least 70% of the days in August 2010. Winter concentrations were the highest between 04:45 and 07:45 and again between 17:45 and 21:45, the times when people would cook and heat their houses against the cold in the evenings, indicating that domestic fuel burning, in this case mostly coal, has an impact on the PM10 levels. Even if most households are electrified in eMbalenhle, residents may still prefer to use domestic fuel, at least for space heating.

 

Several studies have considered the health impact of air pollution on children and infants [12-14]. Children in eMbalenhle may be more exposed to ambient PM10 concentrations than infants and adults, because they spend more time outdoors by walking to school, playing outside during school breaks and have sport activities in the afternoons [15]. Infants will be mostly indoors. However, if there are indoor sources of PM10 such as domestic fuel use, these infants may be exposed to even higher concentrations than outdoors. The adults living in eMbalenhle may have different exposure levels, depending on their occupation and age. Caregivers and the elderly may be exposed to high levels of PM10 if they mostly stay indoors and use domestic fuel. The exposure levels of workers may differ depending on their occupation and whether they work indoors or outdoors. [16] showed that outdoor air pollution in urban areas in South Africa was estimated to cause 3.7% of the national mortality from cardiopulmonary disease and 5.1% of mortality attributable to cancers of the trachea, bronchus and lung in adults aged 30 years and older, and 1.1% of mortality in children under 5 years of age.

 

The results of the human health risk assessment showed that the infant had the highest calculated dose per kilogram body weight, followed by the child and then the adult, yet the risk was the same for all life stages. The reason for the infant's higher dose compared to the other life stages was due to the breathing rate relative to body weight being greater in infants than in adults. For example, the volume of air passing through the lungs of a resting infant is twice that of a resting adult per unit body weight, which implies that twice the amount of chemical may be taken up by the infant than by the adult under identical exposures. The breathing rate in both boys and girls decreases steadily as the child grows older [17]. A study [11] showed that exposure to even moderate levels of air pollution was associated with increased respiratory symptoms in healthy infants. Ambient air quality standards for pollutants do not distinguish between different life stages, in other words there are not different benchmark concentrations for the different life stages, although air quality standards are supposed to protect even sensitive individuals.

 

It is envisaged that children who are exposed to pollutants that may have developmental effects or are mutagenic, will be especially susceptible to exposure to such pollutants. The mechanism of action of a pollutant in the human body is therefore important but unfortunately not known for most pollutants. The USEPA therefore suggests that in cases where children are more affected by a pollutant than an adult, an adjustment is needed. In such cases, a 10 fold adjustment is recommended for exposure before 2 years of age, a 3 fold adjustment for exposure between 2 and 16 years of age and no adjustment after age 16 years [18]. This adjustment was not applied in this study since the chemical composition of the PM10 was not determined.

 

 

Conclusion

The study found that even though eMbalenhle is surrounded by industries and other sources of PM10, emissions at ground level from domestic fuel burning, may contribute mostly to the levels of particulate pollution in eMbalenhle, especially in winter. The results of the HHRA indicated that the infant, child and adult are at equal risk from exposed to the same levels of PM10 for the same duration and individuals are more at risk during winter than summer. More studies should be conducted to assess the indoor exposure to air pollution focussing on the more vulnerable groups such as infants, the elderly and those suffering from other respiratory and cardiovascular diseases.

 

 

Competing interests

The authors declare that they have no competing interests

 

 

Authors’ contributions

This study formed the main study of a M-Tech degree for Nomsa Thabethe. Nomsa Thabethe: Carried out the fieldwork, data analysis and compilation of the draft manuscript. Professor Jacobus Engelbrecht (supervisor), Dr. Caradee Wright (co-supervisor) and Mrs Maria Oosthuizen: Assisted to conceptualise the study and assisted with manuscript preparation. All the authors have read and approved the final version of the manuscript.

 

 

Acknowledgments

We would like to thank Tshwane University of Technology (TUT), The National Association for Clean Air (NACA) and the Council for Scientific and Industrial Research (CSIR) for funding the study. We thank Dr Rebecca Garland (CSIR) for re-drawing Figure 3.

 

 

Tables and figures

Table 1: Safe average daily doses of the different life-stage scenarios

Table 2: Field average daily doses of the different life-stage scenarios (winter)

Table 3: Field average daily doses of the different life-stages scenarios (summer)

Table 4: The results of the calculated hazard quotients (FADD/SADD)

Table 5: The results of the calculated hazard quotients (Field Concentration/NAAQS)

Figure 1: 24-hour PM10 averages monitored with the TOPAS Monitor and by the DEA monitoring station in winter (August 2010)

Figure 2: 24-hour PM10 averages monitored with the TOPAS monitor and by DEA monitoring station in summer (February 2011)

Figure 3: PM10 concentration versus time of day for August 2010 (winter)

Figure 4: Correlation of the 24-hour PM10 averages monitored with the TOPAS monitor and by the DEA monitoring station in winter

Figure 5: Correlation of the 24-hour PM10 averages monitored with the TOPAS monitor and by the DEA monitoring station in summer

 

 

References

  1. Pope CA, Dockey DW. Health effects of fine particulate air pollution: Lines that Connect. Journal of the Air & Waste Management Association, 2006; 56(6):710. Google Scholar

  2. Vallius M, Jassen NAH, Heinrich J, Hoek G, Ruuskanen J, van Grieken CR, de Hartog JJ, Kreyling WG, Pekkanen J. Sources and elemental composition of ambient PM5 in three European cities. Science of the total environment. 2005; 337(1-3):147-162. PubMed | Google Scholar

  3. Darquenne C, Paiva M, Prisk GK. 2000. Effect of gravity on aerosol dispersion and deposition in the human lung after periods of breath holding. Journal of applied physiology, University of California. 2000; 89(5):1787-1792. PubMed | Google Scholar

  4. South Africa. National Environmental Management: Air Quality Act (Act No. 39). February 24 2004. South Africa. Government Gazette, 476 (27318). Google Scholar

  5. Muller E, Diab RD, Binedell M, Hounsome R. Health risk assessment of kerosene usage in an informal settlement in Durban, South Africa. Atmospheric Environment. 2003. 37(15):2015-2022. PubMed | Google Scholar

  6. Matooane M, Diab, RD. Health risk assessment for sulphur dioxide pollution in South Africa, South Africa. Arch Environ Health. 2003; 58(12): 763-770. PubMed | Google Scholar

  7. USEPA. Child-Specific Exposure Factors Handbook, Chapter 6 - Inhalation Rates. 2011. USA: Washington. USEPA. Google Scholar

  8. WHO. Air quality guidelines for particulate matter, ozone, nitrogen dioxide and sulfur dioxide, Global update, Summary of risk assessment. 2006. Geneva. WHO. Google Scholar

  9. Lemly AD. Evaluation of the Hazard Quotient method for Risk Assessment of Selenium Ecotoxicology and Environmental Safety. 1996; 35(2):156-162. Google Scholar

  10. An X, Hou Q, Li N, Zhai, S. Assessment of human exposure level to PM10 in China. Atmospheric Environment. 2013; 70:376-386. PubMed | Google Scholar

  11. Wiriya W, Prapamontol T, Chantara S. PM10-bound polycyclic aromatic hydrocarbons in Chiang Mai (Thailand): seasonal variations, source identification, health risk assessment and their relationship to air-mass movement. Atmospheric Research. 2013; 124: 109-122. PubMed | Google Scholar

  12. Sram RJ, Binkova B, Dostal M, Merkerova-Dostalova M, Libalova H, Milcova A, Rossner R Jr, Rossnerova A, Schmuczerova J, Svecova V, Topinka J and Votavova H. Health impact of air pollutants to children. Int J Hyg Environ Health. 2013; 216(5)533-540. PubMed | Google Scholar

  13. Stern G, Latzin P, Roosli M, Fuchs O, Proietti E, Kuehni C, Frey U. A Prospective Study of the Impact of Air Pollution on Respiratory Symptoms and Infections in Infants. American Journal of Respiratory Critical Care Medicine. 2013; 187(12): 1341-1348. PubMed | Google Scholar

  14. Batterman S, Feng-Chiau S, Chunrong J, Naidoo RN, Robins T, Naik I. Manganese and lead in children's blood and airborne particulate matter in Durban, South Africa. Science of the Total Environment. 2011; 409(6):1058-1068. PubMed | Google Scholar

  15. Barnes B, Mathee A and Moiloa K. Assessing child time-activity patterns in relation to indoor cooking fires in developing countries: a methodological comparison. Int J Hyg Environ Health. 2005; 208(3): 219-225. PubMed | Google Scholar

  16. Norman R, Cairncross E, Witi J, Bradshaw D. Estimating the burden of disease attributable to urban outdoor air pollution in South Africa in 2000. South African Medical Journal. 2007; 97(8 part2):782-90. PubMed | Google Scholar

  17. WHO. Principles for evaluating health risks in children associated with exposure to chemicals. International Programme on Chemical Safety (IPCS) Environmental Health Criteria document (EHC-237). http://www.who.int/ipcs/features/ehc/en/index.html. Accessed 4th February 2010. 2006.

  18. USEPA. Supplemental Guidance for Assessing Susceptibility from Early-Life Exposure to Carcinogens. 2005. USA: Washington DC. USEPA. PubMed | Google Scholar