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. 2021 Jan 3;23(8):12252–12271. doi: 10.1007/s10668-020-01167-1

COVID-19 lockdowns reduce the Black carbon and polycyclic aromatic hydrocarbons of the Asian atmosphere: source apportionment and health hazard evaluation

Balram Ambade 1,, Tapan Kumar Sankar 1, Amit Kumar 1, Alok Sagar Gautam 2,, Sneha Gautam 3
PMCID: PMC7779106  PMID: 33424424

Abstract

Abstract

The entire world is affected by Coronavirus disease (COVID-19), which is spreading worldwide in a short time. India is one of the countries which is affected most, therefore, the Government of India has implemented several lockdowns in the entire country from April 25, 2020. We studied air pollutants (i.e., PM2.5, Black Carbon (BC), and Polycyclic Aromatic Hydrocarbons (PAHs) level, and observed significantly sudden reduced. In India, most of the anthropogenic activities completely stopped. Therefore, we studied the levels of BC, PAHs and PM2.5 concentrations, their sources apportion, and health risk assessment during normal days, lockdown (from lockdown 1.0 to lockdown 4.0) and unlock down 1.0 situation at Sakchi, Jamshedpur city. It was observed that lockdowns and unlock down situations BC, PAHs and PM2.5 concentrations were significantly lower than regular days. We applied the advanced air mass back trajectory (AMBT) model to locate airborne particulate matter dispersal from different directions to strengthen the new result. The diagnostic ratio analyses of BC shows that wood burning contribution was too high during the lockdown situations. However, during normal days, the PAHs source profile was dedicated toward biomass, coal burning, and vehicle emission as primary sources of PAHs. During the lockdown period, emission from biomass and coal burning was a significant contributor to PAHs. The summaries of health risk assessment of BC quantified an equal number of passively smoked cigarettes (PSC) for an individual situation was studied. This study focuses on the overall climate impact of pandemic situations.

Graphic abstract

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Keywords: COVID-19, Black carbon, PAHs, Backward trajectory, Health risk assessment

Introduction

The world is facing an extremely challenging situation due to the feast of coronavirus disease (COVID-19) infectious diseases caused by a recently discovered coronavirus. Based on the increasing rate of COVID-19 worldwide, the World Health Organization (WHO) has announced the COVID-19 as an ‘international pandemic’. The government of many countries declared lockdown in their countries as a containment strategy after mid of March. According to WHO, 215 countries were seriously affected by a coronavirus (COVID-19) disease before June 1, 2020. Due to COVID-19 diseases, over 6.2 million infection cases and 374,229 death were conformed reported throughout the world (WHO 2020b). The first COVID-19 positive person was confirmed reported on January 30, 2020, in India, and the first death was confirmed reported on March 12, 2020 (WHO 2020a). COVID-19 is still increasing day-to-day in India. Due to this pandemic scenario, India’s Prime Minister declared a public curfew on March 22, 2020. Furthermore, India (GoI) government announced a nationwide lockdown (phase I) for more than half a month (21 days) that started from March, 25 to April 1 4, 2020. Phase II was for 19 days from April, 15 to May 3, 2020. Phase III & IV was for 14 days each i.e., started from 4th May to 31st May 2020. To control COVID-19, GoI recommended the Indian states and citizens to stringently maintain the social distancing ways as a precautionary tactic. Although on one side, the COVID-19 outbreak was an extreme condition for human life, on the other side, it has had specific positive influences on the natural situation. In this present work, we had evaluated the effect on the atmospheric concentration of various pollutants such as black carbon (BC), and Polycyclic Aromatic Hydrocarbons (PAHs)) during regular days, different phases of lockdown, and unlock down 1.0.

The BC and PAHs are major constitutes of PM2.5 in the atmosphere. BC and organic carbon (OC) are two essential components of carbonaceous aerosols, which are the most significant segments of airborne particles (Prasad et al. 2018). Some new studies reported that BC might be second-most elevated compared to the greenhouse effect (GHE) and CO2 (Liu et al. 2018). Furthermore, BC is also responsible for glacier melting due to its deposition on snow’s surface (Prasad et al. 2018). BC has the physical property to absorb visible light because of its dark or intense black color (Cachier 1995; Hansen et al. 1984). As a result, it produces a strong heating effect in the Himalayan–Tibetan region (Lau et al. 2010). BC can serve as CCN (cloud condensation nuclei) and affect clouds’ microphysical properties when it is mixed with water-soluble aerosol compositions (Riemer et al. 2010; Rose et al. 2011). Due to smaller size and irregular morphology, BC may cause severe health problems such as mutagenic/carcinogenic pollutants like polycyclic aromatic hydrocarbons (PAHs) and can penetrate deeply into the bronchial part (Janssen et al. 2012). Day-to-day BC emissions have been increasing due to energy demands, industrialization, urbanization, uncontrolled agricultural waste burning, and forest fires in the East and South Asia region (Rastogi et al. 2016; Vadrevu et al. 2015). According to Ramanathan and Carmichael 2008, BC emitted 20% from bio-fuel burning, 40% from open biomass burning and fossil fuel burning. Previous research reported that Asia was the highest BC emission producer in 2000 (Ohara et al. 2007).

Polycyclic aromatic hydrocarbons (PAHs) are organic chemical pollutants with two or more aromatic-fused rings fused (Arey and Atkinson 2003; IARC 1984). PAHs are emitted from both natural and anthropogenic processes. In atmosphere, chief natural sources of PAHs are volcanic eruption fires and forest fires (Baek et al. 1991) while primary anthropogenic sources are coal combustion, biomass burning, petroleum, coke and metal production, etc. (Zhang and Tao 2008). Mainly PAHs are emitted from vehicle emission (Bull 2003; Liu, Liu, Lin, Mostert et al. 2010; Wang et al. 2007), industrial activities, during energy production, and incomplete burn of carbonaceous materials (Xu et al. 2006; Cristale et al. 2012). The study of PAHs receives significant concerns from the last few decades because of its harmful properties such as carcinogenic, teratogenic, and mutagenic properties (Boeuf et al. 2016). Almost 95% of PAHs are associated with size below 3 µm (Venkataraman et al. 1994).

In this study, we assessed the variation in BC, PM2.5 and PAH data in Jamshedpur city, India during normal days, lockdown 1.0, lockdown 2.0, lockdown 3.0, lockdown 4.0, and unlock down 1.0 in the COVID-19 pandemic. This study helps to understand the conditions of atmosphere, sources appropriation, and health risk assessment of Jamshedpur city during COVID-19 (Table 1).

Table 1.

BC, PM2.5 and PAHs concentrations data of normal days, different lockdown situations, and unlock down situations at Sakchi, Jamshedpur

BC PM2.5 PAHs
Min Max Mean SD Min Max Mean SD Min Max Mean SD
ND 6.61 16.45 9.40 2.73 91.67 205.67 136.26 32.16 128.81 150.52 135.70 24.60
LD 1.0 1.19 2.44 1.85 0.36 26.37 62.61 41.39 8.33 12.81 16.04 14.92 03.84
LD 2.0 1.31 2.79 2.24 0.55 25.39 69.88 43.75 12.45 15.97 16.46 16.19 02.81
LD 3.0 1.07 3.35 2.69 0.71 29.11 58.00 45.50 9.14 14.52 16.91 15.46 05.85
LD 4.0 2.25 5.27 4.11 1.02 30.41 79.35 52.99 16.21 33.62 42.23 16.16 10.56
ULD 1.0 2.97 9.64 5.64 1.68 59.34 120.54 86.48 15.77 53.60 66.32 61.42 15.95

ND = Normal Days, LD 1.0 = Lockdown 1.0, LD 2.0 = Lockdown 2.0, LD 3.0 = Lockdown 3.0, LD 4.0 = Lockdown 4.0 and ULD 1.0 = Unlock down 1.0

Sampling site

BC measurements were made in the Sakchi, Jamshedpur city (220 80′ N Longitude and 860 20′ E Latitude), located in the southern part of Jharkhand, India. Sakchi is the heart of Jamshedpur. The city stretches over the Chota Nagpur Plateau (CNP) area and covers approximately 6500 km2. Sackhi is the central part of Jamshedpur and is a very densely populated area. The total population of the city of Jamshedpur is around 1.3 million (according to the 2011 census). The city of Jamshedpur is surrounded on one side by the Dalma Hills which include dense forested areas, green mountains, and world-renowned large industrial conglomerates such as TATA Motors and TATA Iron and Steel Company (TISCO). The Adityapur Industrial Development Authority (AIDA) area is also located in the city of Jamshedpur. More than 1000 industries (small, medium, and large industries) operate in Adityapur in the AIDA region. The main source of pollution in this area is emissions from city building construction, traffic emissions, road construction, and industrial activities. The map of the sampling location is shown in Fig. 1. Due to the large number of industries and road networks that are the main source of BC, PM2.5 and PAH in the atmosphere of the city of Jamshedpur. BC, PAHs, and PM2.5 aerosols were monitored in three situations (normal days, different lockdown, and unlock down situations) environment or we can say that six situations, i.e., normal days (ND), lockdown 1.0 (LD 1.0), lockdown 2.0 (LD 2.0), lockdown 3.0 (LD 3.0), lockdown 4.0 (LD 4.0), and unlock down 1.0 (ULD 1.0).

Fig. 1.

Fig. 1

Satellite aerial view of the sampling site at Sakchi, Jamshedpur city

Measurements and methodologies

Measurement of BC mass concentrations

The various essential methodologies to measure the BC mass concentration compared to other techniques like particle soot absorption photometer, thermal oxidation/reflectance, coefficient of haze tape sample, etc. (Allen et al. 1999). Aethalometer is the most straightforward technique to measure the BC mass concentrations because, the mass concentration of BC aerosol is measured with the help of seven different wavelengths 370 nm, 470 nm, 525 nm, 590 nm, 660 nm, 880 nm, and 940 nm. This technique is based on a filter that methods the attenuation of light because the particle’s mass is deposited on a filter. The air inlet was fitted to the roof of the building. Atmospheric air pumped over an inlet at the flow rate (nearby 5 LPM) that collides on a quartz filter. BC mass concentrations were reported on the time basis of every 5 min. According to recent research, 880 nm is the standard wavelength for measuring BC mass concentration because BC is the main absorber of light in this particular wavelength; further, aerosol components have unrelated absorption (Weingartner et al. 2003). At 880 nm, a light beam from an extraordinary-intensity light-emitting-diode lamp was transferred over the sample collected on the filter strip. Continuous real-time observation of BC mass concentrations was performed from three different situations i.e., normal days, lockdown (from LD 1.0 to LD 4.0), and unlock down situations. Lockdown and unlock down situations were entirely affected by the COVID-19 pandemic.

Measurement of PM2.5 and PAHs concentrations

The sampling was conducted using a mini volume sampler (Envirotech Model APM 550) operating at a continuous flow rate of 16.5 L/m3. PTFE filter (47 mm, Merck, catalog no- PM2547050) was used to collect particulate associated PAHs. Before examining, the filter was weighed and kept in a desiccator. Weight balance having a single pan-top loading digital weight balance (VWR, Model no: VWR1611-2263: with Weighing Chamber L × W × H: 162 × 171 × 225 mm) was used. The foundation contamination was checked using operational blanks (unexposed filters), which were handled simultaneously with field tests. Furthermore, the sample filter was kept in a culture box. These samples were retained at 4 °C for preservation. The sample was kept in the refrigerator until analysis. In this study, a total of 16 PAHs were analyzed. 16 priority USEPA-PAHs were extracted using soxhlet extraction. To avoid dust loss, the filter was divided into two or more pieces and put into 200 mL distillation vessels for 10 h. Using the dichloromethane (DCM) solvent in which the extraction cap is primarily dropped and illustrations almost more than 97% recovery rates. After the extraction process was done. The extracted volume was decreased to 10 mL by rotary evaporator. The temperature of the chiller was maintained for condensing DCM. The solvent boiling of the, such that the entire extraction period is decreased whereas the vaporized solvent reduces rapidly for reprocessing, dropping the amount of total solvent necessary. Sodium sulfate—silica gel column (glass column of 30 cm long and 3 cm in diameter) was used for extract purification. Further, 99% pure nitrogen gas was used again and again to reduce the volume of purified extract up to 1–2 mL and then quantified by advanced Gas Chromatography (GC- FID, Agilent 7890B) coupled with a flame ionization detector (FID) equipped with capillary column HP- 5MS (30 m × 0.25 mm i.d × 0.25 µm). Nitrogen gas was used as carrier gas with a flow rate of 2 mL min−1. In the splitless mode, 1 µL of each sample was injected into GC-FID. The oven temperature was started at 60 °C for 3 min and increased up to 320 °C at a rate of 5 °C min−1 and kept for 20 min. The 16 USEPA priority PAH concentrations were quantified with the help of the peak area of spectra and retention time. The field and laboratory blank samples were isolated and then examined similarly to the field sample. The PAH compound was not identified in the blank samples.

Source apportionment method of BC mass concentration and PAHs

In this study, a handy aethalometer was used to reveal the source apportionment of BC mass concentration. Many methods were used to clarify the source apportionment of BC mass concentration, such as positive matrix factorization (PMF), the macro-tracer method, principal component analysis (PCA), chemical mass balance (CMB), the aethalometer model, and other specialized models (Florou et al. 2017; Thepnuan et al. 2019; Briggs and Long 2016; Belis et al. 2013; Larsen et al. 2012; Favez et al. 2010). But Aethalometer is one of the easiest methods. This model characterizes fewer source-category (e.g., traffic emissions and wood burning); however, it only requires a different-wavelength light absorption dataset (Zotter et al. 2017). Significant sources of BC mass concentrations were incomplete combustion of biofuel burning and fossil fuel in the atmosphere. To characterize the BC mass sources of regional emissions from the sources mentioned above, we must determine the percentage difference in BC measured at two wavelengths i.e., BC370 and BC880.

i.e.,%differenceofBC=BC370-BC880/BC880. 1

From Eq. (1), if the percentage difference of BC value was reported to a negative fraction, it suggested that BC emission comes out from fossil fuel (e.g., diesel, petrol, etc.). And if a difference in the percentage of BC value was reported to positive fraction, it suggested that BC emission comes out from wood burning (e.g., domestic use products like coal, forest fire, dry leaf, etc.) (Wang et al. 2011).

We can have characterized the different sources of PAHs from diagnostic ratio analysis. For diagnostic ratio analysis, the biomass burning, coal burning, traffic emission, and industry emissions were analyzed. We also described the fire count data and air backward trajectory to analyses the source apportionment of BC mass concentrations, PAHs, and PM2.5 concentrations.

Assessment of health risks of BC

According to modern scientific studies and current research, exposure to BC may cause serious health issue to humans such as non-cancer (respiratory-related problem, cardiovascular diseases) and cancer (lung cancer) diseases in humans (Niranjan and Thakur 2017; De Prins et al. 2014; Magalhaes et al. 2018). The health risks of passive smoking are equivalent to the health risk of BC (e.g., Muller and Muller 2013; Wu et al. 2018; Van der Zee et al. 2016). Since both show identical characteristics. Mainly three main features show to compare the health risk between passive smoking and BC aerosol, (1) both show alike health effects, (2) contact to environmental tobacco smoke (ETS) and atmospheric BC contamination, and (3) both risks have the similar exposure way, i.e., through inhalation (Van der Zee et al. 2016). According to Van der Zee et al. 2016 had developed a model by which we can easily determine the health hazard evaluation, which is grounded on ETS. The value of ETS was used to calculate the health risk of BC pollution. Four health-related issues were detected with the help of this model. The four health issues are cardiovascular mortality (CM), lung cancer (LC), low birth weight (LBW), and percentage lung function decrement of school-aged children (PLFDSC). All four health-related issues are noticeable by reference to both ETS and BC pollution (Kelly and Fussell 2015; WHO 2014; Oberg et al. 2010). The calculation part of health risk estimation was primarily dependent on relative risks (RRs), comparable to a different health issue for ETS exposure and air pollutant like BC; where RR refers to the prospect of growing an illness induced by contact to air pollutants (WHO 2003; Rothman et al. 2008). The connection between a health-related risk issue and a specified change in BC aerosol was identified by a meta-analysis of recorded concentration–response functions (CRFs). Since the particular fitness issue (i.e., R), the BC concentration increases by one µg m−3, comparable to the number of passively smoked cigarettes (PSC) (Van der Zee et al. 2016).

Therefore, R is written as

R=lnRRBC/ΔConc/lnRRETS/expectednumberofPSC 2

where [ln(RRBC)/ΔConc] = the consequential risks for variation in ΔConcentration (i.e., 1 µg m−3) of BC. RRBC = RR of BC concerning particular health issues. [ln(RRETS)/assumed number of PSC] = the ensuing risks of ETS exposure for the expected number of PSC per day. RRETS = RR of ETS for the particular health issue.

The value of RRBC and RRETS is resultant from precisely organized assessments and can be summarized to implement the relevant, yet immature, health hazard estimations. The value of RRBC and RRETS was taken from the selected reference paper (Pani et al. 2020). The expected number of PSC per day is different for different health risk issues. For the child of a non-smoking mother, the expected number of PSC per day is 7 for CVM, LC and LBW (Van der Zee et al. 2016). The assumed number of PSC per day is 9 in the case of PLFDSC. The following formula calculated the corresponding numbers of PSC per day (i.e., NPSC: passive cigarette-equivalence),

NPSC=ΔBC×R 3

And

ΔBC=BCrep-BCbac 4

where BCrep = Reported Black Carbon and BCbac = Background Black Carbon.

In this recent study, our aim to reported only health risk estimates of BC pollution but not reported the inclusive concern of disease because of ETS exposure or BC effluence (Wu et al. 2018), which are accessible to understand for the public as well as the policymakers. Our assessment was depended on the WHO-based review of Van der Zee et al. (2016), where the 14 daily cigarette intake smokers from North-West Europe and the united state (US). In this new study, our target to report the health hazards of atmospheric BC effluence corresponding to residents of Jamshedpur city in the different situation during the COVID-19 pandemic i.e., for normal days, lockdown (from lockdown 1.0 to lockdown 4.0) and unlock down 1.0 situations, who may be the probable receptor as matched with passive cigarette smoking.

Evaluation of health risks due to PAHs

The health hazard allied with PAHs contact was calculated using the Toxicity equivalent concentration (TEQ) equation (Yu et al. 2008). The equation shows the summation of projected cancer risk related to BaP for all PAHs having carcinogenic potential, which can be designed by multiplying the concentration of every carcinogenic PAHs and Toxicity equivalence factor (TEF).

TEQ=Ci x TEFi 5

where Ci = Separate PAHs concentration and TEFi = the toxic equivalency factor

TEFi value was given by Nisbet and Lagoy (1992); 0.01 for Phe, Flt, and Pyr; 0.01 value for Chr, Ant, and B(ghi)P; 0.1 value for BaA, BkF, and IcP and 1 value for BaP and DBahA. Moreover, the exposure risk due to individual PAHs can be quantitatively calculated by Incremental lifetime cancer risk (ILCR) (EPA. 1991; U.S. Chen and Liao 2006; Peng et al. 2011). ILCR was measured by considering the corresponding lifetime average daily dose (LADD) of PAHs by allowing for dual age group adults (age 70 years) and children (age 6 years). LADD demonstrates the quantity of uncertain chemical consumption per kg of body mass per day and harms health when detected by the body for an extended period. The following equation is used for the expression and assessment of LADD and ILCR.

LADDmgkg-1day-1=Cs×CF×IR×EF×ED/BW×AT 6
ILCR=LADD×CSFCancerOralSlopeFactor 7

where C01s means the quantity of PAHs’ transformed concentration concerning TEQ assessment in airborne particulate (ng m−3). In the present study, the ILCR value was evaluated for adult and child, where parameters were, CF means the unit change factor (1 × 10−6 mg kg−1), IR was the air inhalation rate (m3 day−1), EF means the exposure frequency (day year−1), ED means the lifetime exposure period. BW means the Bodyweight (kg), AT means the averaging time for carcinogens (days), and CSF means the inhalation cancer slope factor (3.85 mg kg−1 day−1) (Peng et al. 2011). The detail of the parameter designated in Table 4.

Table 4.

Health risk assessment due to PAHs exposure to children and adults over the study area

Exposure parameter Unit Child Adult
BWa kg 18 60
ATb years 70 70
IRc m3 day−1 10 20
EFd days year−1 365 365
EDb years 6 24
Age group Normal days Lockdown (1.0–4.0) Unlock down (1.0)
LADD (mg kg−1 day−1) ILCR LADD (mg kg−1 day−1) ILCR LADD (mg kg−1 day−1) ILCR
Children 7. 9 × 10−5 3.06 × 10−6 4.0 × 10−5 1.55 × 10−6 4.4 × 10−5 1.68 × 10−6
Adult 1.91 × 10−6 7.36 × 10−6 9.7 × 10−5 3.72 × 10−6 1.05 × 10−5 4.05 × 10−6

aICMR (2009)

bFerreira-Baptista and De-Miguel (2005)

cSoltani et al. (2015)

dKumar et al. (2013)

eUSEPA (2011)

Results and discussion

Black carbon mass concentration variation during the study period

The satellite study through the GIOVANNI NASA website demonstrated the BC surface mass concentration monthly 0.5 × 0.625 deg. [MERRA-2 Model M2TMNXAER v 5.12.4] µg m−3 at three situations i.e., Normal Days, different lockdown (from lockdown 1.0 to lockdown 4.0), and Unlock down 1.0-situations, as shown in Fig. 2. According to the GIOVANNI NASA website, BC mass concentration was reported to be highest during normal days i.e., approx. 3 µg m−3 to 4 µg m−3 compared to lockdown situation (from lockdown 1.0 to lockdown 4.0) and unlock down 1.0 situation. In lockdown situation, BC mass concentration was approx. 1.88 µg m−3 to 2.77 µg m−3 and in the unlock down situation was approx. 2.33 µg m−3 to 3.22 µg m−3. It was seen that in the unlock down situation, the BC mass concentration was a little bit high as associated with the lockdown situation. This is because during a lockdown situation, all traffic transportation, industries activities were closed, and unlock down situation, most of the traffic transportation and some industries were open. The eastern part and the northern part of Indian had a more BC concentration compared to the rest part of the country i.e., the Indo-Gangetic Plain (IGP) region had more BC concentration in all three situations. i.e., during normal days, lockdown (from lockdown 1.0 to lockdown 4.0) situations and unlock down 1.0 situation. It was clearly shown in Fig. 2. Simultaneously, we conducted fieldwork to determine the BC mass concentrations. BC mass concentrations were analyzed for 12 h a day during six situations. The averaged BC mass concentrations were noticed to be about 9.40 ± 2.73 µg m−3, 1.85 ± 0.36 µg m−3, 2.24 ± 0.55 µg m−3, 2.69 ± 0.71 µg m−3, 4.11 ± 1.02 µg m−3 and 5.64 ± 1.68 µg m−3 during normal days, lockdown 1.0, lockdown 2.0, lockdown 3.0, lockdown 4.0, and unlock down 1.0, respectively. On normal days, maximum and minimum BC mass concentrations were16.45 µg m−3 and 6.61 µg m−3, respectively. BC’s concentration was very high because all activities such as industries, construction work, traffics, roads were working during normal days. In different lockdown situations, BC’s maximum and minimum concentration was 1.07 µg m−3 (during lockdown 3.0) and 5.27 µg m−3 (during lockdown 4.0), respectively. The low BC mass concentrations were observed because all activities such as construction work, industries work, transportation work, traffic roads were closed during lockdown situations. In unlock down situations, maximum and minimum BC mass concentrations were 2.97 µg m−3 and 9.64 µg m−3, respectively. During these days, BC’s mass concentration was moderate, i.e., neither high as in normal days nor low like lockdown situations. This is because during these days some activities were open like transport work, traffic roads are open but industries work was not fully open and maybe some industries were open. During the whole study, BC mass concentration was varied from 1.07 to 16.45 µg m−3. It was seen that the BC mass concentration continuously decreased throughout lockdown situations and again a little bit increasing during unlock down situations as revealed in Fig. 3.

Fig. 2.

Fig. 2

Time average map of Black carbon surface mass concentration monthly 0.5 × 0.625 deg. [MERRA-2 Model M2TMNXAER v 5.12.4] µg m−3 at three different situations a Normal Days, b Lockdown 1.0, 2.0, 3.0, & 4.0, and c unlock down 1.0

Fig. 3.

Fig. 3

Mass concentration with stand deviation of PM2.5 and BC at different situations i.e., normal days (ND), lockdown 1.0 (LD 1.0), lockdown 2.0 (LD 2.0), lockdown 3.0 (LD 3.0), lockdown 4.0 (LD 4.0), and unlock down 1.0 (ULD 1.0) at Sakchi, Jamshedpur

PM2.5 and PAHs concentration variation during the study period

Like BC mass concentration, PM2.5 concentrations and 16 PAHs were also determined in different situations i.e., Normal Days, Lockdown 1.0, Lockdown 2.0, Lockdown 3.0, & Lockdown 4.0, and unlock down 1.0 as shown in Fig. 3. On normal days’ maximum and minimum of PM2.5 concentrations were 91.67 µg m−3 and 205.67 µg m−3, respectively, and the minimum concentration of PAHs was 128.81 ng m−3, and maximum concentration was 150.52 ng m−3. The concentration of PM2.5 and PAHs was high because all activities like industries traffic transport, roads, construction works were open during normal days. In different lockdown situations, minimum and maximum concentrations of PM2.5 were 25.39 µg m−3 (during lockdown 2.0) and 79.35 µg m−3 (during lockdown 4.0), respectively, and minimum concentration of PAHs was 12.81 ng m−3 (during lockdown 1.0), and maximum concentration was 42.23 ng m−3 (during lockdown 4.0). The low PM2.5 and PAH concentrations were observed because all activities such as industries work, transportation work, construction work, traffic roads were closed during lockdown situations. In the unlock down situation, maximum and minimum PM2.5 concentrations were 59.34 µg m−3 and 120.54 µg m−3, respectively, and minimum concentration of PAHs was 53.60 ng m−3 and the maximum concentration was 66.32 ng m−3. During these days the PM2.5 and PAH’s concentration was moderate i.e., neither high as in normal days nor low like lockdown situations because during these days in some activities were open, such as transport work, traffic road, etc. but industries work was not fully open, somewhere maybe some industries were open. The averaged PM2.5 concentrations were noticed to be about 136.26 ± 32.16 µg m−3, 41.39 ± 8.33 µg m−3, 43.75 ± 12.45 µg m−3, 45.50 ± 9.14 µg m−3, 52.99 ± 16.21 µg m−3, and 86.48 ± 15.77 µg m−3 during normal days, lockdown 1.0, lockdown 2.0, lockdown 3.0, lockdown 4.0, and unlock down 1.0, respectively. During the whole study, PM2.5 concentrations were varied from 25.39 to 205.67 µg m−3. It was seen that the PM2.5 concentrations were continuously decreasing during lockdown situations (from lockdown 1.0 to lockdown 4.0) and again a little bit increasing during unlock down 1.0 situations as shown in Fig. 3. The averaged PAHs concentrations were noticed to be about 135.70 ± 24.60 ng m−3, 14.92 ± 3.84 ng m−3, 16.19 ± 2.81 ng m−3, 15.46 ± 5.85 ng m−3, 16.16 ± 10.56 ng m−3, and 61.42 ± 15.95 ngvm−3 during normal days, lockdown 1.0, lockdown 2.0, lockdown 3.0, lockdown 4.0, and unlock down 1.0, respectively. And during study of PAHs concentrations was varied from 12.81 to 150.52 ng m−3, and it was seen in Fig. 4 that the PAHs concentrations were continuously decreasing during lockdown situations, and again small numbers of concentrations were increasing during unlock down 1.0 situations.

Fig. 4.

Fig. 4

Concentration (ng m−3) of PAHs at three different situations i.e., normal days (ND), lockdown 1.0–4.0 (LD 1-4), and unlock down 1.0 (ULD 1) situations at Sakchi, Jamshedpur

In all phases of lockdown, the anthropogenic activities were closed. As a result, fewer air pollutants were coming into the atmosphere. In the current study, it was reported that Anthracene (Ant) concentrations were maximum i.e., 11.98 ± 1.38 ng m−3 and Dibenzo[ah]anthracene (DBahA) concentrations were minimum i.e., 5.82 ± 0.72 ng m−3 during normal days. During lockdown 1.0 situations, Pyrene (Pyr) concentrations were maximum i.e., 1.18 ± 0.30 ng m−3, and Naphthalene (Nap) concentrations were minimum i.e., 0.61 ± 0.16 ng m−3. Indeno[123-cd]pyrene (IcP) concentration was maximum i.e., 1.12 ± 0.13 ng m−3, and Benzo[a]pyrene (BaP) concentration was minimum i.e., 0.56 ± 0.24 ng m−3 in lockdown 2.0 situation, and Acenaphthene (Ace) concentration was maximum i.e., 1.39 ± 0.37 ng m−3, and Benzo[a]pyrene (BaP) concentration was minimum i.e., 0.48 ± 0.34 ng m−3 in lockdown 3.0 situation. During lockdown 4.0 situations, Indeno[123-cd]pyrene (IcP) concentration was maximum i.e., 1.29 ± 1.00 ng m−3, and Benzo[a]pyrene (BaP) concentration was minimum i.e., 0.66 ± 0.0.41 ng m−3. Indeno[123-cd]pyrene (IcP) concentration was maximum i.e., 4.95 ± 0.69 ng m−3, and Acenaphthylene (Acy) concentration was minimum i.e., 2.67 ± 0.66 ng m−3 during unlock down 1.0 situation. The 16 PAH concentrations are reported in Table 2. The regular emission PAHs concentrations in Sakchi, Jamshedpur city was due to local residence burning such as burning coal, wood, biomass, kerosene, traffic emission, industrialization. The whole research study shows that the concentrations of all air pollutants such as BC, PAHs and PM2.5 were decreased during the lockdown as compare to normal days and unlock down situations due to the COVID-19 pandemic.

Table 2.

The concentration of PAHs (ng m−3) in six different situations

Abbr ND LD 1.0 LD 2.0 LD 3.0 LD 4.0 ULD 1.0
PAHs SD PAHs SD PAHs SD PAHs SD PAHs SD PAHs SD
Nap 8.25 1.16 0.61 0.16 0.88 0.09 1.15 0.34 0.87 0.53 3.39 0.58
Acy 6.02 1.55 0.73 0.16 1.08 0.14 0.88 0.28 1.01 0.78 2.67 0.66
Ace 7.04 0.89 1.38 0.40 0.86 0.17 1.39 0.37 1.10 0.52 3.44 0.62
Flu 7.64 0.71 0.74 0.38 0.98 0.14 0.61 0.56 0.86 0.65 3.11 0.78
Phe 10.94 1.86 1.02 0.16 1.08 0.15 1.13 0.41 1.01 0.53 4.17 0.98
Ant 11.98 1.38 0.90 0.09 1.34 0.20 0.63 0.42 0.92 0.57 4.71 1.24
Flua 10.25 1.56 0.82 0.22 1.06 0.20 1.24 0.49 1.12 0.75 4.27 1.49
Pyr 7.04 2.05 1.18 0.30 1.09 0.14 1.14 0.40 1.05 0.50 2.81 1.25
Chr 10.29 2.24 0.86 0.20 0.88 0.16 1.11 0.37 1.01 0.66 4.71 1.15
BaA 7.70 1.68 0.72 0.25 1.09 0.19 0.65 0.40 1.01 0.92 4.79 1.18
BbF 10.56 1.83 1.13 0.37 1.07 0.21 0.92 0.34 1.16 0.81 3.59 1.37
BkF 11.88 1.79 0.98 0.20 0.98 0.19 0.90 0.26 0.97 0.56 3.68 1.22
BaP 6.55 3.15 0.74 0.15 0.56 0.24 0.48 0.34 0.66 0.41 3.55 1.43
DBahA 5.82 0.72 0.91 0.17 1.10 0.32 1.10 0.35 1.11 0.72 3.81 0.96
B(ghi)P 6.06 0.64 1.14 0.26 1.02 0.15 0.85 0.19 1.03 0.64 3.78 0.38
IcP 7.69 1.39 1.06 0.36 1.12 0.13 1.27 0.31 1.29 1.00 4.95 0.69
ΣPAH 135.70 0.67 14.92 0.09 16.19 0.05 15.46 0.09 16.16 0.14 61.42 0.34

SD standard deviation, Abbr abbreviation

Naphthalene (Nap), Acenaphthylene (Acy), Acenaphthene (Ace), Fluorene (Flu), Phenanthrene (Phe), Anthracene (Ant), Fluoranthene (Flua), Pyrene (Pyr), Chrysene (Chr), Benzo[a]anthracene (BaA), Benzo[b]fluoranthene (BbF), Benzo[k]fluoranthene (BkF), Benzo[a]pyrene (BaP), Dibenzo[ah]anthracene (DBahA), Benzo[ghi]perylene (B(ghi)P), Indeno[123 cd]pyrene (IcP)

Source apportionment of BC and PAHs concentration

The sources of BC mass concentration and PAH concentration may have the same but their technique is different from characterized the source apportionment. The source recognition of BC mass concentration was determined by the aethalometer technique. Although, this model characterized some selective source-category such as wood burning and traffic emissions. According to SAFAR 2010, the burning of coal is a major source of BC mass concentration into the atmosphere, and coal burning is the highest source of energy that supplies 76% of our requirement in India. An examination of BC estimated at UV (370 nm) frequencies and near IR (880 nm) frequencies was made, which is great for the source characterization of BC (Srivastava et al. 2012). Bio-fuel consuming and horticulture fires have been perceived as the most significant source of BC over the Indo-Gangetic Basin (IGB) territories (Venkataraman et al. 2006). The source separates between wood-consuming and petroleum products in various circumstances, i.e., ordinary days, lockdown-1.0, lockdown-2.0, lockdown-3.0, lockdown-4.0, and unlock down-1.0-circumstance. The origins of BC mass concentration are processes, i.e., the natural process such as volcanic eruptions, forest fires, and anthropogenic exercises like coal consumption, consuming petroleum products, biomass consumption for agribusiness, and vehicular developments yet the significant sources are a petroleum product and wood-consuming. It was reported that in normal days’ and unlock down 1.0-situation aids of wood burning and fossil fuel are approximately the same, but during different lockdown situations, fossil fuel contribution was low compared to wood burning. This is because of the movement of vehicles and industries shut down, i.e., all activities were closed. The contribution of BC toward various wavelength during numerous circumstances are depicted in the Fig. 5.

Fig. 5.

Fig. 5

Fractional contribution of BC measured at 370 nm and 880 nm at six different situations i.e., normal days, lockdown 1.0, lockdown 2.0, lockdown 3.0, lockdown 4.0, and unlock down 1.0-situations at Sakchi, Jamshedpur

Source appropriation of PAHs

As per an ongoing investigation of PAHs, the symptomatic proportion (DR) examination strategy has been utilized for PAHs’ source division (Tobiszewski and Namieśnik 2012). The proportion of IcP/(IcP + B(ghi)P), Flua/(Flua + Pyr), BaA/(BaA + Chr), BaP/B(ghi)P, and Ant/(Ant + Phe) was utilized to recognize the wellsprings of PAHs in the air. The proportion of IcP/(IcP + B(ghi)P) is a pointer of petrogenic, oil-consuming, and biomass coal ignition source. Proportion esteem < 0.2 and > 0.5 characteristic of Petrogenic and biomass burning. The proportion of esteem lies between the scope of 0.2–0.5 the source will demonstrate the oil burning (Ravindra et al. 2008). The proportion estimation of IcP/(IcP + B(ghi)P) was determined 0.54 before lockdown and 0.49 during the lockdown period, which recommended the outflow from biomass and coal ignition over the investigation site. On the off chance that the proportion of Flua/(Flua + Pyr) is < 0.1 the characteristic source is Unburned oil/Petrogenic, if esteem saw between 0.4 and 0.5, the source is petroleum derivative ignition if esteem watched > 0.5 the source distinguished as coal burning and biomass (Yunker et al. 2002; De La Torre-Roche et al. 2009). In this current investigation, the proportion of Flua/(Flua + Pyr) was seen 0.55 Before lockdown and 0.53 during the lockdown period recommending PAHs emanation from biomass and coal burning. The proportion of BaA/(BaA + Chr) is < 0.2 and > 0.35 demonstrates ignition and petrogenic source (Yunker et al. 2002; Tobiszewski and Namiesnik 2012). BaA/(BaA + Chr) proportion esteem was seen to be 0.42 and 0.45 before lockdown and during the lockdown period, separately, proposing the coal ignition and biomass source. BaP/B(ghi)P proportion determines traffic emanation, < 0.6 esteem shows non-traffic source and worth > 0.6 demonstrates the traffic wellspring of discharge. BaP/B(ghi)P proportion esteem was determined 1.19 before the lockdown period and 0.56 during the lockdown period recommending traffic source before lockdown and non-traffic source during the lockdown. The proportion of Ant/(Ant + Phe) characteristic of pyrogenic and petrogenic sources. The off chance that the worth discovered < 0.1 assigns petrogenic and > 0.1 shows pyrogenic sources (Pies et al. 2008). Insect/(Ant + Phe) proportion esteem was found to be 0.50 and 0.46 before lockdown and during lockdown period individually, proposing the pyrogenic source. The entire count of indicative proportion investigation has appeared in Table 4.

The Diagnostic proportion examination inferred that biomass, vehicle emanation, and coal consumption were essential drivers of PAHs before the lockdown period. Yet, during the lockdown period, the outflow from consuming biomass and coal was a significant supporter of PAHs.

Backward trajectories analysis

Backward trajectory analysis is a model to explain the transportation routes of air pollutants. It also determines the direction of airflow to describe the possible region of sources before reaching a specific target position. The back trajectories were calculated for two situations, i.e., normal days and different lockdown situations (from lockdown 1.0 to lockdown 4.0) along with unlock down 1.0. The overall trajectories were prepared using a global environmental dataset online program NCEP (National Centers for Environmental Prediction) Climate Forecast System and Meteorological Data Explorer developed by Center for Global Environmental Research (CGER), Japan and Igor software. Backward trajectories were calculated at different heights (altitude) from 0 to 4000 m with an other color band. The fire count data downloaded from NASA FIRMS (https://firms.modaps.eosdis.nasa.gov/data/download/DL_FIRE_M6_76896.zip). The fire count data were also incorporated along with back trajectories in Fig. 6. The back trajectory analysis indicated that the air mass (air pollutants) originating from different places from different heights to enter the target places. According to the backward trajectory analysis model, the air-born particulate matter migrated from the northeast part of our country during normal days. Maximum air particulate mass was coming from the Himalayan region, and little air particulate mass was coming from the Bay of Bengal (BoB). It was likewise reported that some air particulate mass was traveled from western countries such as Iran, Afghanistan, and Pakistan, and some air particulate mass was migrated from Nepal and Sikkim as shown in Fig. 6a. It was seen that the air-born particulate matter migrated from the northeast part of, the Indian Ocean, the northern part of our country as well as BoB. The maximum air particulate mass was migrated from western countries mainly from Afghanistan and Pakistan. But the height of trajectories is moderate during lockdown situations (from lockdown 1.0 to lockdown 4.0) and unlock down situations as shown in Fig. 6b.

Fig. 6.

Fig. 6

7-days air mass back trajectories as well as fire count graph on the two different situations a normal days and b different lockdown and unlock down situations, at an altitude level of 500 m above ground level, over the sampling side

Health risk assessment of BC and PAHs

In the current study, we tried to report the health risk assessment expressed in three different situations i.e., normal days, different lockdown situations (from lockdown 1.0 to lockdown 4.0), and unlock down 1.0 situations at Sakchi, Jamshedpur city. The summary of health risk assessment indicated in an identical number of PSC for an individual period of investigation as shown in Table 3. We consider that the day to a daily exposure level of BC for the people living in Jamshedpur city was equivalent to the day-to-day mean BC (balance load concerning the background BC) level. The BCbac concentration level was calculated as the 1.25th percentile of BCrep concentrations for the datasets (Rupakheti et al. 2017) at three different situations i.e., 6.72 µg m−3 (normal days), 1.14 µg m−3 (during different lockdown situations) and 3.13 µg m−3 (during unlock down 1.0-situation) for Jamshedpur city in this study. On normal days, the health risk assessment of BC concentration was reported as high as 4.81, 9.79, 8.62, and 19.66 passive cigarettes comparable concerning the risk of CVM, LC, LBW, and PLEDSC, respectively. And during different lockdown situations (from lockdown 1.0 to lockdown 4.0) and unlock down 1.0-situation, the health risk assessment of BC concentration was reported as low as 2.69, 5.48, 4.82, 11 and 4.51, 9.17, 8.07, 18.41 passive cigarettes comparable concerning the risk of CVM, LC, LBW, and PLEDSC, respectively. It was noticed that the health risk issue is higher on normal days compared to the COVID-19 pandemic (during different lockdown situations and unlock down 1.0-situation).

Table 3.

The health risk estimates of BC communicated into equivalent numbers of PSC per day concerning four various health issues

Parameters Normal Days Lockdown (1.0–4.0) Unlock down 1.0
CVM 4.81 2.69 4.51
LC 9.79 5.48 9.17
LBW 8.62 4.82 8.07
PLEDSC 19.66 11 18.41

PSC passively smoked cigarettes, CVM cardiovascular mortality, LC lung cancer, LBW low birth weight, PLFDSC percentage lung function decrement of school-aged children

In this recent study, the health risk of 16 USEPA priority PAHs was analyzed. The LADD’S value for carcinogenic PAHs for an adult was found to be 1.91 × 10−6, 9.7 × 10−5 and 1.05 × 10−5 mg kg−1 day−1 over the study site during normal days, different lockdown situations (from lockdown 1.0 to lockdown 4.0) and unlock down 0.1 situations, respectively. Established on LADD value over the study spot, ILCR value for an adult was estimated at 7.36 × 10−6, 3.72 × 10−6 and 4.05 × 10−6 during normal days, different lockdowns and unlock down 0.1 situations, respectively. During normal days, different lockdown situations and unlock down 0.1 situations, the LADD value for children was found to be 7.9 × 10−5, 4.0 × 10−5 and 4.4 × 10−5 mg kg−1 day−1, respectively. ILCR value for children was estimated at 3.06 × 10−6, 1.55 × 10−6 and 1.68 × 10−6 during normal days, different lockdown and unlock down situations, respectively. Furthermore, the excess lifetime cancer risk (ELCR) was estimated by some ILCR for adult and ILCR values for the child over the study sites. The ELCR values for normal days, different lockdown situations and during unlock down situations were 10.42 × 10−6, 5.27 × 10−6, and 5.73 × 10−6, respectively. The ELCR value were lies between the acceptable limit 10−6–10−4 specified by regulatory agency USEPA (USEPA. 1989) during normal days, different lockdown, and unlock down situations. A concise of the health hazards assessment of PAHs has been given in Table 4. The result showed that the risk level was acceptable over the study site during normal days, different lockdown and unlock down situations.

Conclusion

Measurements of BC mass concentrations, PAHs concentration, and PM2.5 were reported in different situations i.e., normal days, lockdown-1.0, lockdown-2.0, lockdown-3.0, lockdown-4.0, and unlock down-1.0-situation. The averaged BC mass concentrations were 9.40 ± 2.73 µg m−3, 1.85 ± 0.36 µg m−3, 2.24 ± 0.55 µg m−3, 2.69 ± 0.71 µg m−3, 4.11 ± 1.02 µg m−3, and 5.64 ± 1.68 µg m−3 during normal days, lockdown-1.0, lockdown-2.0, lockdown-3.0, lockdown-4.0, and unlock down-1.0 situation, respectively, at Sakchi, Jamshedpur city. The averaged PM2.5 mass concentrations were 136.26 ± 32.16 µg m−3, 41.39 ± 8.33 µg m−3, 43.75 ± 12.45 µg m−3, 45.50 ± 9.14 µg m−3, 52.99 ± 16.21 µg m−3, and 86.48 ± 15.77 µg m−3 during normal days, lockdown-1.0, lockdown-2.0, lockdown-3.0, lockdown-4.0, and unlock down-1.0-situation, respectively, at Sakchi, Jamshedpur city. BC mass concentrations and PM2.5 concentration varies from 1.07 µg m−3 to 16.45 µg m−3 and 25.39 µg m−3 to 205.67 µg m−3 during study period. During normal days, BC mass concentration and PAHs concentration as high compared to different lockdown and unlock down situations and moderate during unlock down situations; neither is higher than normal days nor low compared to different lockdown situations. The average PAH concentrations were 135.70 ± 24.60 ng m−3, 14.92 ± 3.84 ng m−3, 16.19 ± 2.81 ng m−3, 15.46 ± 5.85 ng m−3, 16.16 ± 10.56 ng m−3, and 61.42 ± 15.95 ng m−3 during normal days, lockdown-1.0, lockdown-2.0, lockdown-3.0, lockdown-4.0, and unlock down-1.0 situation, respectively, at study side. PAH concentration varies from 12.81 to 135.70 ng m−3 during the study period. PAHs concentration was low during different lockdown situations because, during lockdown situations, all the activities were closed. The industry work, transport work, construction work, traffic movement, etc., was shut down due to the COVID-19 pandemic. As a result, air pollutants’ emission was less compared to normal days in Jamshedpur city atmosphere. According to the diagnostic ratio analysis of BC, it was noticed that the influence of wood burning as well as fossil fuel was the same in the normal days and unlock down. It was also reported that the fossil fuel contribution was low as compared to wood burning during different lockdown situations. The diagnostic ratio analysis of PAHs suggests that biomass, coal burning and vehicle emission were primary causes of PAHs during the study period. The summary of health risk assessment indicated an equal number of PSC for an individual month of investigation. The health hazard assessment of BC concentration was reported as 4.81, 9.79, 8.62, 19.66; 2.69, 5.48, 4.82, 11 and 4.51, 9.17, 8.07, 18.41 during normal days, lockdown (from lockdown-1.0 to lockdown-4.0) and unlock down-1.0 situations in Sakchi, Jamshedpur city, the passive cigarettes comparable concerning the risk of CVM, LC, LBW, and PLEDSC, respectively. The excess lifetime cancer risk (ELCR) value was reported to be 10.42 × 10−6, 5.27 × 10−6, and 5.73 × 10−6 for normal days, different lockdown situations (from LD 1.0 to LD 4.0) and during unlock down (ULD 1.0) situation.

Acknowledgements

The present study was supported by the Science & Engineering Research Board (SERB) (Grant No. ECR1) Government of India. The Sanction Order number of the project is ECR/2017/000597. The author thanks NASA FIRMS (Fire Information for Resource Management System), GIOVANNI NASA, Fire Archive for fire count data by Moderate Resolution Imaging Spectroradiometer (MODIS) C6. The Meteorological Data Explorer developed by the Center for Global Environmental Research (CGER), Japan (METEX, http://db.cger.nies.go.jp/metex/trajectory.html) and for the provision of trajectories used in the publication.

Funding

Science & Engineering Research Board (SERB) Government of India. The Sanction Order number of the project is ECR/2017/000597.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Footnotes

Publisher's Note

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Change history

1/9/2021

Authors email address has been corrected

Contributor Information

Balram Ambade, Email: bambade.chem@nitjsr.ac.in.

Alok Sagar Gautam, Email: phyalok@gmail.com.

Sneha Gautam, Email: gautamsneha@gmail.com.

References

  1. Allen GA, Lawrence J, Koutrakis P. Field validation of a semicontinuous method for aerosol black carbon (aethalometer) and temporal patterns of summertime hourly black carbon measurements in southwestern PA. Atmospheric Environment. 1999;33:817–823. [Google Scholar]
  2. Arey J, Atkinson R. Photochemical reactions of PAH in the atmosphere. In: Douben PET, editor. PAHs: An ecotoxicological perspective. New York, NY: John Wiley and Sons Ltd; 2003. pp. 47–63. [Google Scholar]
  3. Baek SO, Field RA, Goldstone ME, Kirk PW, Lester JN, Perry R. A review of atmospheric polycyclic aromatic hydrocarbons: sources, fate and behavior. Water, Air, and Soil Pollution. 1991;60:79–300. [Google Scholar]
  4. Belis CA, Karagulian F, Larsen BR, Hopke PK. Critical review and metaanalysis of ambient particulate matter source apportionment using receptor models in Europe. Atmospheric Environment. 2013;69:94–108. [Google Scholar]
  5. Boeuf B, Fritsch O, Martin-Ortega J. Undermining European environmental policy goals? The EU water framework directive and the politics of exemptions. Water. 2016;8:388. [Google Scholar]
  6. Briggs NL, Long CM. Critical review of black carbon and elemental carbon source apportionment in Europe and the United States. Atmospheric Environment. 2016;144:409–427. [Google Scholar]
  7. Bull, K. (2003). Protocol to the 1979 convention on long-range trans boundary air pollution on persistent organic pollutants: The 1998 agreement for the UNECE region, Geneva.
  8. Cachier H. Combustion carbonaceous aerosols in the atmosphere: implications for ice core studies. In: Robert JD, editor. Ice core studies of global biogeochemical cycles. Berlin: Springer; 1995. pp. 313–346. [Google Scholar]
  9. Chen SC, Liao CM. Health risk assessment on human exposed to environmental polycyclic aromatic hydrocarbons pollution sources. Science of the Total Environment. 2006;366:112–123. doi: 10.1016/j.scitotenv.2005.08.047. [DOI] [PubMed] [Google Scholar]
  10. Cristale J, Silva FS, Zocolo GJ, Marchi MRR. Influence of sugarcane burning on indoor/outdoor PAH air pollution in Brazil. Environmental Pollution. 2012;169:210–216. doi: 10.1016/j.envpol.2012.03.045. [DOI] [PubMed] [Google Scholar]
  11. De La Torre-Roche RJ, Lee W-Y, Campos-Díaz SI. Soil–borne polycyclic aromatic hydrocarbons in El Paso, Texas: analysis of a potential problem in the United States/Mexico border region. Journal of Hazardous Materials. 2009;163:946–958. doi: 10.1016/j.jhazmat.2008.07.089. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. De Prins S, Dons E, Van Poppel M, IntPanis L, Van de Mieroop E, Nelen V, Cox B, Nawrot TS, Teughels C, Schoeters G, Koppen G. Airway oxidative stress and inflammation markers in exhaled breath from children are linked with exposure to black carbon. Environment International. 2014;73:440–446. doi: 10.1016/j.envint.2014.06.017. [DOI] [PubMed] [Google Scholar]
  13. Favez O, Haddad EII, Piot C, Boreave A, Abidi E, Marchand N, Jaffrezo J-L, Besombes J-L, Personnaz MB, Sciare J, Wortham H, George C, D’Anna B. Inter-comparison of source apportionment models for the estimation of wood burning aerosols during wintertime in an Alpine city (Grenoble, France) Atmospheric Chemistry and Physics. 2010;10:5295–5314. [Google Scholar]
  14. Ferreira-Baptista L, De-Miguel E. Geochemistry and risk assessment of street dust in Luanda: Angola. A tropical urban environment. Atmospheric Environment. 2005;39:4501–4512. [Google Scholar]
  15. Florou K, Papanastasiou DK, Pikridas M, Kaltsonoudis C, Louvaris E, Gkatzelis GI, Patoulias D, Mihalopoulos N, Pandis SN. The contribution of wood burning and other pollution sources to wintertime organic aerosol levels in two Greek cities. Atmospheric Chemistry and Physics. 2017;17:3145–3163. [Google Scholar]
  16. Hansen ADA, Rosen H, Novakov T. The aethalometer: an instrument for the realtime measurements of optical absorption by aerosol particles. Science of the Total Environment. 1984;36:191–196. [Google Scholar]
  17. IARC. (1984). Polynuclear aromatic compounds. Part 1. Chemical environmental and experimental data IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, vol. 32. International Agency for Research on Cancer, Lyon, France. [PubMed]
  18. ICMR. (2009). Nutrient requirements and recommended dietary allowances for Indians. A report of the expert group of the Indian Council of Medical Research Hyderabad, India: National Institute of Nutrition.
  19. Janssen NH, Janssen N, Gerlofs NM. Health effects of black carbon. Copenhagen: World Health Organization; 2012. [Google Scholar]
  20. Kelly FJ, Fussell JC. Air pollution and public health: emerging hazards and improved understanding of risk. Environmental Geochemistry and Health. 2015;37:631–649. doi: 10.1007/s10653-015-9720-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Kumar M, Furumai H, Kurisu F, Kasuga I. Tracing source and distribution of heavy metals in road dust: Soil and soak away sediment through speciation and isotopic fingerprinting. Geoderma. 2013;211–212:8–17. [Google Scholar]
  22. Larsen BR, Gilardoni S, Stenstrom K, Niedzialek J, Jimenez J, Belis CA. Sources for PM air pollution in the Po Plain, Italy: II. Probabilistic uncertainty characterization and sensitivity analysis of secondary and primary sources. Atmospheric Environment. 2012;50:203–213. [Google Scholar]
  23. Lau KM, Kim MK, Kim KM, Lee WS. Enhanced surface warming and accelerated snow melt in the Himalayas and Tibetan Plateau induced by absorbing aerosols. Environmental Research Letters. 2010;5:025204. [Google Scholar]
  24. Liu Y, Yan C, Zheng M. Source apportionment of black carbon during winter in Beijing. Science of the Total Environment. 2018;618:531–541. doi: 10.1016/j.scitotenv.2017.11.053. [DOI] [PubMed] [Google Scholar]
  25. Magalhaes S, Baumgartner J, Weichenthal S. Impacts of exposure to blackcarbon, elemental carbon, and ultrafine particles from indoor and outdoor sources on blood pressure in adults: a review of epidemiological evidence. Environmental Research. 2018;161:345–353. doi: 10.1016/j.envres.2017.11.030. [DOI] [PubMed] [Google Scholar]
  26. Mostert MMR, Ayoko GA, Kokot S. Application of chemometrics to analysis of soil pollutants. TrAC Trends in Analytical Chemistry. 2010;29:430–435. [Google Scholar]
  27. Muller, R. A., & Muller, E. A. (2013). Air pollution and cigarette equivalence. Berkeley Earth 47.
  28. Niranjan R, Thakur AK. The toxicological mechanisms of environmental soot (black carbon) and carbon black: Focus on oxidative stress and inflammatory pathways. Frontiers in Immunology. 2017;8:763. doi: 10.3389/fimmu.2017.00763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Nisbet ICT, Lagoy PK. Toxic equivalency factors (TEFs) for polycyclic aromatic hydrocarbons (PAHs) Regulatory Toxicology and Pharmacology. 1992;16(3):290–300. doi: 10.1016/0273-2300(92)90009-x. [DOI] [PubMed] [Google Scholar]
  30. Oberg, M., Jaakkola, M. S., Prüss-Üstün, A., Schweizer, C., & Woodward, A. (2010). Second Hand Smoke, Assessing the Environmental Burden of Disease at National and Local Levels, vol. 18. World Health Organization, Geneva, Environmental Burden of Disease Series. http://www.who.int/quantifying_ehimpacts/publications/SHS.pdf.
  31. Ohara T, Akimoto H, Kurokawa J, Horii N, Yamaji K, Yan X, Hayasaka T. An Asian emission inventory of anthropogenic emission sources for the period 19802020. Atmospheric Chemistry and Physics. 2007;7:4419–4444. doi: 10.5194/acp-7-4419-2007. [DOI] [Google Scholar]
  32. Pani SK, Wang SH, Lin NH, Chantara S, Lee CT, Thepnuan D. Black carbon over an urban atmosphere in northern peninsular Southeast Asia: Characteristics, source apportionment, and associated health risks. Environmental Pollution. 2020;259(2020):113871. doi: 10.1016/j.envpol.2019.113871. [DOI] [PubMed] [Google Scholar]
  33. Peng C, Chen WP, Liao XL, Wang ME, Ouyang ZY, Jiao WT, Bai Y. Polycyclic aromatic hydrocarbons in urban soils of Beijing: Status, sources, distribution and potential risk. Environmental Pollution. 2011;159:802–808. doi: 10.1016/j.envpol.2010.11.003. [DOI] [PubMed] [Google Scholar]
  34. Pies C, Hoffmann B, Petrowsky J, Yang Y, Ternes TA, Hofmann T. Characterization and source identification of polycyclic aromatic hydrocarbons (PAHs) in river bank soils. Chemosphere. 2008;72:1594–1601. doi: 10.1016/j.chemosphere.2008.04.021. [DOI] [PubMed] [Google Scholar]
  35. Prasad P, Raman MR, Ratnam MV, Chen WN, Rao SVB, Gogoi MM, Kompalli SK, Kumar KS, Babu SS. Characterization of atmospheric black carbon over a semi-urban site of Southeast India: Local sources and long-range transport. Atmospheric Research. 2018;213:411–421. [Google Scholar]
  36. Ramanathan V, Carmichael G. Global and regional climate changes due to black carbon. Nature Geoscience. 2008;1:221–227. [Google Scholar]
  37. Rastogi N, Singh A, Sarin MM, Singh D. Temporal variability of primary and secondary aerosols over northern India: Impact of biomass burning emissions. Atmospheric Environment. 2016;125:396–403. [Google Scholar]
  38. Ravindra K, Sokhi R, Van Grieken R. Atmospheric polycyclic aromatic hydrocarbons: Source attribution, emission factors and regulation. Atmospheric Environment. 2008;42:2895–2921. [Google Scholar]
  39. Riemer N, West M, Zaveri R, Easter R. Estimating black carbon aging time-scales with a particle-resolved aerosol model. Journal of Aerosol Science. 2010;41:143–158. [Google Scholar]
  40. Rose D, Gunthe SS, Su H, Garland RM, Yang H, Berghof M, Cheng YF, Wehner B, Achtert P, Nowak A, Wiedensohler A, Takegawa N, Kondo Y, Hu M, Zhang Y, Andreae MO, Pöschl U. Cloud condensation nuclei in polluted air and biomass burning smoke near the mega-city Guangzhou, China—Part 2: Size-resolved aerosol chemical composition, diurnal cycles, and externally mixed weakly CCN-active soot particles. Atmospheric Chemistry and Physics. 2011;11:2817–2836. doi: 10.5194/acp-11-2817-2011. [DOI] [Google Scholar]
  41. Rothman KJ, Greenland S, Lash TL. Modern epidemiology. Philadelphia, PA: Wolters Kluwer/Lippincott Williams & Wilkins; 2008. pp. 53–77. [Google Scholar]
  42. Rupakheti D, Adhikary B, Praveen PS, Rupakheti M, Kang S, Mahata KS, Naja M, Zhang Q, Panday AK, Lawrence MG. Pre-monsoon air quality over Lumbini, a world heritage site along the Himalayan foothills. Atmospheric Chemistry and Physics. 2017;17:11041–11063. [Google Scholar]
  43. Soltani N, Keshavarzi B, Moore F, Tavakol T, Lahijanzadeh AR, Jaafarzadeh N, Kermani M. Ecological and human health hazards of heavy metals and polycyclic aromatic hydrocarbons (PAHs) in street dust of Isfahan metropolis, Iran. Science of the Total Environment. 2015;505:712–723. doi: 10.1016/j.scitotenv.2014.09.097. [DOI] [PubMed] [Google Scholar]
  44. Srivastava AK, Singh S, Pant P, Dumka UC. Characteristics of black carbon over Delhi and Manora Peak—a comparative study. Atmospheric Science Letters. 2012 doi: 10.1002/asl.386,223-230(July). [DOI] [Google Scholar]
  45. Thepnuan D, Chantara S, Lee CT, Lin NH, Tsai YI. Molecular markers for biomass burning associated with the characterization of PM2.5 and component sources during dry season haze episodes in Upper South East Asia. Science of the Total Environment. 2019;658:708–722. doi: 10.1016/j.scitotenv.2018.12.201. [DOI] [PubMed] [Google Scholar]
  46. Tobiszewski M, Namieśnik J. PAH diagnostic ratios for the identification of pollution emission sources. Environmental Pollution. 2012;162:110–119. doi: 10.1016/j.envpol.2011.10.025. [DOI] [PubMed] [Google Scholar]
  47. USEPA. (2011). Exposure factors handbook edition. EPA/600/R-09/052F. Washington, DC: National Center for Environmental Assessment, Office of Research and Development, U.S. Environmental Protection Agency 20460.
  48. Vadrevu KP, Lasko K, Giglio L, Justice C. Vegetation fires, absorbing aerosols and smoke plume characteristics in diverse biomass burning regions of Asia. Environmental Research Letters. 2015;10:105003. doi: 10.1088/1748-9326/10/110/105003. [DOI] [Google Scholar]
  49. Van der Zee SC, Fischer PH, Hoek G. Air pollution in perspective: health risks of air pollution expressed in equivalent numbers of passively smoked cigarettes. Environmental Research. 2016;148:475–483. doi: 10.1016/j.envres.2016.04.001. [DOI] [PubMed] [Google Scholar]
  50. Venkataraman C, Habib G, Kadamba D, Shrivastava M, Leon J-F, Crouzille B, Boucher O, Streets DG. Emissions from open biomass burning in India: Integrating the inventory approach with high resolution Moderate Resolution Imaging Spectroradiometer (MODIS) active-fire and land cover data. Global BiogeochemicalCycles. 2006;20:GB2013. doi: 10.1029/2005GB002547. [DOI] [Google Scholar]
  51. Venkataraman C, Lyons JM, Friedlander SK. Size distributions of polycyclic aromatic hydrocarbons and elemental carbon. 1. Sampling, measurement methods, and source characterization. Environmental Science and Technology. 1994;28:555–562. doi: 10.1021/es00053a005. [DOI] [PubMed] [Google Scholar]
  52. Wang Y, Hopke PK, Utell MJ. Urban-scale spatial-temporal variability of black carbon and winter residential wood combustion particles. Aerosol and Air Quality Research. 2011;11:473–481. [Google Scholar]
  53. Wang Z, Li K, Lambert P, Yang C. Identification, characterization and quantitation of pyrogenic polycyclic aromatic hydrocarbons and other organic compounds in tire fire products. Journal of Chromatography A. 2007;1139(1):14–26. doi: 10.1016/j.chroma.2006.10.085. [DOI] [PubMed] [Google Scholar]
  54. Weingartner E, Saathoff H, Schnaiter M, Streit N, Bitnar B, Baltensperger U. Absorption of light by soot particles, determination of the absorption coefficient by means of aethalometers. Journal of Aerosol Science. 2003;34:1445–1463. [Google Scholar]
  55. WHO. (2020b). World Health Organization, Coronavirus Disease (COVID-2019) Situation Reports– Situation Report – 116; [accessed 2020 May 15]. https://www.who.int/docs/default-source/coronaviruse/situation-reports/20200515-covid-19-sitrep-116.pdf?sfvrsn=8dd60956_2.
  56. WHO (World Health Organization). (2003). Health Aspects of Air Pollution with Particulate Matter, Ozone and Nitrogen Dioxide. http://www.euro.who.int/document/e79097.
  57. WHO (World Health Organization). (2014). Burden of Disease from Air Pollution. http://www.who.int/phe/health_topics/outdoorair/databases/FINAL_HAP_AAP_BoD_24March2014.pdf, 02.02.16.
  58. World Health Organization. (2020a). Novel coronavirus – Thailand (ex-China).
  59. Wu J, Lu J, Min X, Zhang Z. Distribution and health risks of aerosol black carbon in a representative city of the Qinghai-Tibet Plateau. Environmental Science and Pollution Research. 2018;25(20):19403–19412. doi: 10.1007/s11356-018-2141-9. [DOI] [PubMed] [Google Scholar]
  60. Xu S, Liu W, Tao S. Emission of polycyclic aromatic hydrocarbons in China. Environmental Science and Technology. 2006;40:702–708. doi: 10.1021/es0517062. [DOI] [PubMed] [Google Scholar]
  61. Yu Y, Guo H, Liu Y, Huang K, Wang Z, Zhan X. Mixed uncertainty analysis of polycyclic aromatic hydrocarbon inhalation and risk assessment in ambient air of Beijing. Journal of Environmental Science. 2008;20:505–512. doi: 10.1016/s1001-0742(08)62087-2. [DOI] [PubMed] [Google Scholar]
  62. Yunker M, MacDonald R, Vingarzan R, Mitchell R, Goyette D, Sylvestre S. PAHs in the Fraser River basin: a critical appraisal of PAH ratios as indicators of PAH source and composition. Organic Geochemistry. 2002;33:489–515. [Google Scholar]
  63. Zhang YX, Tao S. Emission of polycyclic aromatic hydrocarbons (PAHs) from indoor straw burning and emission inventory updating in China. Annals of the New York Academy of Sciences. 2008;1140:218–227. doi: 10.1196/annals.1454.006. [DOI] [PubMed] [Google Scholar]
  64. Zotter P, Herich H, Gysel M, El-Haddad I, Zhang Y, Močnik G, Hüglin C, Baltensperger U, Szidat S, Prévôt ASH. Evaluation of the absorption Ångstrom exponents for traffic and wood burning in the Aethalometer-based source apportionment using radiocarbon measurements of ambient aerosol. Atmospheric Chemistry and Physics. 2017;17:4229–4249. [Google Scholar]

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