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Environ Monit Assess (2016) 188: 402

DOI 10.1007/s10661-016-5393-1

Meteorology drives ambient air quality in a valley: a case


of Sukinda chromite mine, one among the ten
most polluted areas in the world
Soumya Ranjan Mishra & Rudra Pratap Pradhan &
B. Anjan Kumar Prusty & Sanjat Kumar Sahu

Received: 19 February 2016 / Accepted: 25 May 2016 / Published online: 11 June 2016
# Springer International Publishing Switzerland 2016

Abstract The ambient air quality (AAQ) assessment varied significantly among the monitoring stations sug-
was undertaken in Sukinda Valley, the chromite hub of gesting (i) the distance of sampling location to the mine
India. The possible correlations of meteorological vari- site and other allied activities, (ii) landscape features and
ables with different air quality parameters (PM10, PM2.5, topography and (iii) meteorological parameters to be the
SO2, NO2 and CO) were examined. Being the fourth forcing functions. The area was highly polluted with
most polluted area in the globe, Sukinda Valley has particulate matters, and in most of the cases, the PM
always been under attention of researchers, for level exceeded the National Ambient Air Quality Stan-
hexavalent chromium contamination of water. The mon- dards (NAAQS). The meteorological parameters
itoring was carried out from December 2013 through seemed to play a major role in the dispersion of pollut-
May 2014 at six strategic locations in the residential and ants around the mine clusters. The role of wind direc-
commercial areas around the mining cluster of Sukinda tion, wind speed and temperature was apparent in dis-
Valley considering the guidelines of Central Pollution persion of the particulate matters from their source of
Control Board (CPCB). In addition, meteorological pa- generation to the surrounding residential and commer-
rameters viz., temperature, relative humidity, wind cial areas of the mine.
speed, wind direction and rainfall, were also monitored.
The air quality data were subjected to a general linear Keywords Ambient air quality . Air pollution index .
model (GLM) coupled with one-way analysis of vari- Mining . Particulate matter . Sukinda Valley
ance (ANOVA) test for testing the significant difference
in the concentration of various parameters among sea-
sons and stations. Further, a two-tailed Pearson’s corre-
Introduction
lation test helped in understanding the influence of
meteorological parameters on dispersion of pollutants
Rapid industrialization and urbanization have resulted in
in the area. All the monitored air quality parameters
degradation of environment and its components. Mining in
developing countries like India plays a vital role in the
S. R. Mishra : B. A. K. Prusty (*)
overall economy and simultaneously contribute to envi-
Gujarat Institute of Desert Ecology, PO Box No. 83, Opp. ronmental degradation (Chandra et al. 2014). Air pollution
Changleshwar Temple, Mundra Road, Bhuj, Gujarat 370001, is one of the inevitable impacts of mining activities leading
India to air quality degradation and subsequent health implica-
e-mail: anjaneia@gmail.com tions on humans and animals and also affects plants and
R. P. Pradhan : S. K. Sahu materials. Chromium is one of the most commonly occur-
P.G. Department of Environmental Sciences, Sambalpur ring elements in the earth’s crust and occupies the 21st
University, Jyoti Vihar, Odisha 768019, India position in abundance. Chromite ore mining has become

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402 Page 2 of 17 Environ Monit Assess (2016) 188: 402

essential due to its important uses in stainless steel, chrome operational (02 underground and 10 opencast) and 05
plating, manufacturing of dyes and pigments, leather and are non-operational due to lack of statutory clearances
wood preservation, treatment of evaporative tower water, (Pattnaik et al. 2012). The most common environmental
drilling mud, textiles, ink toners, chemical catalyst, aircraft problems due to mining are (i) large-scale deforestation
and in refractory industries for aluminium-forming bricks. (Saha et al. 2011); (ii) accumulation of huge overburden
Almost entire consumption (98.9 %) is used in ferro- dumps (Maiti 2007); (iii) extensive air, water, soil and
alloys/charge-chrome industry. The elements found in noise pollution (Lad and Samant 2013); (iv) impaired
group VI of the periodic table bear identical properties plant growth with removal of top soil and formation of
but cannot replace chromium due to cost and marginal man-made wastelands (Dhal et al. 2010); (v) formation
advantages. Elemental chromium (Cr) does not occur in of poor soil conditions viz., low nutrient content, poor
nature but is present as ores mainly chromite (FeOCr2O3). water holding capacity, imbalanced pH, toxic heavy
Chromite is the mixture of iron-chromium oxide mineral metal accumulation along with soil erosion, which
and is the only ore of chromium metal (IBM 2013). transfers the heavy metal ions to the nearby water chan-
The overall world reserves of shipping-grade chro- nels (Misra et al. 2004). Chromite mines generate con-
mite are more than 12 billion tonnes. The major siderable quantity of pollutants containing toxic
chromite-producing countries are South Africa, Zimba- hexavalent chromium, a known carcinogen, which con-
bwe, Kazakhstan, Brazil, Turkey, Finland, Russia and tributes to the 10–4000 ppm of total chromium in air,
India, among which South Africa contributes over 95 % water and soil environment (Vijayan and Nikos 2015).
of the total world deposits (Pattnaik et al. 2012). India Airborne emissions occur during each stage of the min-
contributes about 2 % of the total chromite deposits in ing cycle, especially during drilling, blasting, explora-
the world and has reserves of 203 million tonnes (MT). tion, development, construction, operation and transpor-
Of this, about 190 MT (95 %) is mostly concentrated in tation activities. The ancillary developments such as
Sukinda Valley (IBM 2013) and the rest are concentrat- development of different industries like sponge iron,
ed in other states of India, viz., Jharkhand, Karnataka, crushers and railway sidings around the mining area
Tamil Nadu, Andhra Pradesh and Manipur (Fig. 1, IBM also create gaseous and particulate pollutants (Panda
2013). The chromite ore belt at Sukinda is spread over and Barik 2010).
an area of approximately 200 km2 in Jajpur district of Mining operations mobilize large amount of waste
Odisha, India and is a well-known chromite hub in the materials containing minute particles, which are easily
world (Das and Mishra 2010). In India, most of the dispersed by wind. Particulate matter (PM) includes
mining operations are done by opencast method. The both organic and inorganic substances, which could be
chromium ore grade >38 % is marketed directly, where- solid, liquid or suspended in the atmosphere (Davidson
as the ones between 10 and 35 % are stacked as sub- et al. 2005). Particles with aerodynamic diameter
grade ore and kept for further beneficiation. The ore <10 μm (PM10) are of concern for health (Chen et al.
grade <10 % is stacked as overburden dumps (IBM 2005) and environmental problems (Seinfeld and Pandis
2013). The consumption of chromite in India in the 2006). Aerosols with aerodynamic diameter <2.5 μm
organized sector has increased by 25.4 % (IBM 2012). (PM2.5) are responsible for health hazards, as it contains
Though the chromite mining in Sukinda Valley greatly acidity (hydrogen ion) and mutagenic activity (Prusty
contributes towards India’s economic development, at et al. 2005), and those with <1.0 μm size (PM1) contrib-
the same time, it deteriorates natural environment utes to visibility reduction and radiative effects (Berico et
(Tiwary et al. 2005) and hence is listed as the fourth al. 1997). Furthermore, PM has wider impacts on climate,
most polluted area in the world (BSI 2007). Alarming causing direct (absorbing, reflecting and scattering), indi-
concentrations of hexavalent chromium in surface and rect (cloud formation, cloud albedo and lifetime) and semi-
groundwater has affected nearly 2.6 million people in direct (heating and cooling) effects on the global radiative
Sukinda (Mishra and Sahu 2013). budget (Solomon et al. 2007). The gaseous pollutants like
SO2, NO2 and CO are released to the atmosphere by
Mining activities and environmental implications vehicular and other allied activities in the mining area
(Talebi 1997; Katiyar et al. 2003; Madhuri et al. 2003).
Opencast mining in Sukinda Valley was started in Sulphur and nitrogen compounds in both gaseous and
1950s. Of the total 17 mining leases, currently 12 are particulate phases are known to have environmental and

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Environ Monit Assess (2016) 188: 402 Page 3 of 17 402

Fig. 1 Chromite resource map of


India (source: IBM 2013)

health implications (Lee et al. 1999). An overview of air In view of the above specifics, we carried out a study
pollution scenario in other opencast (non-ferrous) mines to assess the level of particulate and gaseous pollutants
around the globe is presented in Table 1. arising from the mining and ancillary activities along
with the meteorological interaction in and around the
chromite belt of Sukinda Valley. The AAQ was moni-
Air pollution index tored from December 2013 through May 2014 to assess
the seasonal variation of air pollutants, inter-pollutant
Air pollution index (API) is an environmental index, correlations and meteorological interactions with the
which describes the overall ambient air quality (AAQ) pollutant concentrations.
status and trend of a particular place based on prescribed
standards. The overall AAQ of a specified area can be
assessed in a better way and quantified in terms of API,
since it represents the cumulative effect of all the pol- Materials and methods
lutants, and provides a succinct view of the overall air
quality of an area, and aids in informed decision and Study area
policy making for prevention of air pollution. It also
provides insights to design air pollution control equip- Sukinda Valley (Fig. 2) is present at the south-eastern
ment, which, for instance, will reduce the level of certain part of India in Jajpur district of Odisha and lies between
pollutants while increasing the level of others. The latitude 21° 00′ N to 21° 05′ N and longitude 85° 44′ E
higher the API value, greater is the level of air pollution to 85° 53′ E (Survey of India toposheet no. 73 G/16, 73
and hence greater is the health risk. The API scale is H/9 and 73 H/13). The Mahagiri hill ranges lie to the
divided into five categories (Table 2). south of Sukinda Valley with an altitude of 300 m above

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402 Page 4 of 17 Environ Monit Assess (2016) 188: 402

Table 1 Air pollutants in the other (non-ferrous) mining clusters throughout the globe

Air quality parameters Comparison with the previous studies

Concentration range Type of industry Location of mine Reference

PM10 (μg/m3) 12–200 Coal mine Zonguldak, Turkey Tecer et al. (2008)
144.8–342.9 Coal mine Dhanbad, Chhattisgarh, India Sing and Pal (2010)
161.39–394.01 Coal mine Jharia coal field, Chhattisgarh, India Mishra et al. (2012)
40.8–171.9 Coal mine Ib valley, Odisha, India Chaulya (2005)
34–153 Lignite mine Western Kachchh, Gujarat, India Prusty (2012)
135.9–271.9 Coal mine Jharia coal field, Chhattisgarh, India Pandey et al. (2014)
44.2–171.9 Coal mine and metal mine Kosova, Mitrovica, Europe Syla et al. (2007)
32–288 Coal mine Talcher coal field, Odisha, India Roy et al. (2012)
338–369 Coal mine Jharia coal field, Chhattisgarh, India Roy et al. (2015)
PM2.5 (μg/m3) 4.55–96.65 Coal mine Zonguldak, Turkey Tecer et al. (2008)
6.6–52.7 Coal mine and metal mine Kosova, Mitrovica, Europe Syla et al. (2007)
SO2 (μg/m3) 1.47–6.14 Coal mine Tirap colliery, Assam, India Sarmah et al. (2012)
8–36.5 Lignite mine Western Kachchh, Gujarat, India Prusty (2012)
10–105 Coal mine Jharia coal field, Chhattisgarh, India Pandey et al. (2014)
3
NO2 (μg/m ) 1.92–2.40 Coal mine Tirap colliery, Assam, India Sarmah et al. (2012)
7.5–77.5 Lignite mine Western Kachchh, Gujarat, India Prusty (2012)
10–70 Coal mine Jharia coal field, Chhattisgarh, India Pandey et al. (2014)
CO (μg/m3) 65–295 Lignite mine Western Kachchh, Gujarat, India Prusty (2012)
4–10 Coal mine Angul-Talcher belt, Odisha, India Suman et al. (2007)

mean sea level (MSL), whereas to the north lie the predominantly due to south-west monsoon. The
Daitari Hill ranges with an altitude of 400 m above relative humidity of the area varies from 65 to
MSL. The valley meanders towards west and then south 93 %. The area mainly comprises of ultramafic
along its slope and is drained by Damsala Nala, which rocks consisting of alternate chromite, dunite, peri-
flows from north-east (NE) to south-west (SW) and dotite and orthopyroxinite bands (Dhakate and
drains into the Brahmani River. The site is located at a Singh 2008). These bands are repeated in a rhyth-
distance of about 140 km from the state capital, mic fashion and synformally folded plunging west
Bhubaneswar. south-west (WSW) at an angle of 100○ to 150○.
Sukinda experiences humid climate, and temper- Hexavalent chromium (Cr VI) in surface water and
ature varies from around 14 to 46 °C. The average groundwater is a major culprit, affecting around 2.6
annual rainfall of the area is around 1500 mm, million people in the area (Mishra and Sahu 2013).

Table 2 API range with air quality and health impacts

Sl. no Index range Quality of air Health concern

1 0–25 Clean air (CA) None/minimal health effect


2 26–50 Light air pollution (LAP) Possible respiratory or cardiac effect for most sensitive group
3 51–75 Moderate air pollution (MAP) Increasing symptoms of respiratory and cardiovascular illness
4 76–100 Heavy air pollution (HAP) Aggravation of heart and lung diseases
5 >100 Severe air pollution (SAP) Serious aggravation of heart and lung diseases Risk of death in children

Ziauddin and Siddiqui (2006)

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Environ Monit Assess (2016) 188: 402 Page 5 of 17 402

Fig. 2 Location map of Sukinda


Valley along with different
mining leases

Mining activities below the groundwater table and Sampling and analysis
discharge of mining effluents to natural water bod-
ies without proper treatment lead to contamination The ambient air sampling was carried out from Decem-
of ground and surface water. ber 2013 through May 2014 at six strategic locations.
Considering the accuracy of the results into account, the
Selection of the monitoring stations monitoring was carried out during dry seasons only, i.e.
in winter (December 2013 to February 2014) and sum-
AAQ monitoring was carried out at strategic locations in mer (March 2014 to May 2014). Sampling was carried
Sukinda Valley following the guidelines of Central Pol- out as per CPCB guidelines and methods. The instru-
lution Control Board (CPCB 2011). The stations were ments were fixed at a height of 3 to 10 m above ground
selected to obtain representative picture of the air quality level in order to get a representative sample avoiding
in the region by considering different characteristic fea- dust lifted from ground (CPCB 2011).
tures, viz., (i) sensitivity of the station, (ii) source of The sampling of particulate and gaseous pollutants was
pollutants, (iii) meteorological parameters such as pre- carried out twice a week at uniform intervals throughout
dominant wind direction, (iv) human settlements, (v) the sampling period (CPCB 2011). For the sampling of
provisions of electricity and safety of the instruments, PM10 (respirable suspended particulate matter (RSPM)),
(vi) height of instrument fixation and (vii) accessibility respirable dust sampler (RDS, make: Ecotech, model:
of the station. The meteorological data were collected by AAS 217 BL) was used. The sampling was carried out
installing an Automatic Weather Monitoring Station for 24 h at an air flow rate of 1.0 to 1.3 m3/min using glass
(AWMS) at mining office of South Kaliapani chromite microfibre filter paper (make: Whatman, type: GF/A, size
mine of M/s OMC Ltd. in Sukinda Valley. The meteo- 20.3 × 25.4 cm). The sampling of PM2.5 was carried out by
rological data for the preceding 1 year (December 2012 fine particulate sampler (FPS, make: Ecotech, model no
to November 2013) was processed using WRPLOT AAS 127) using polytetrafloroethylene (PTFE, diameter
View (Lakes Environmental) software to prepare wind 46.2 mm) filter paper supported by polypropylene ring.
rose diagram, which provided insights on the predomi- The sampling was carried out for 24 h with a fixed air flow
nant wind directions in the study area (Fig. 3). rate of 1 m3/h. The sampling of SO2 and NO2 was carried
From the wind rose diagram, it was learnt that the out by attaching a gaseous attachment (make: Ecotech,
predominant wind direction was from east (E) to west model: AAS 109) with the suction outlet of RDS through
(W) and vice versa followed by NE. Thus, we presumed a suction pipe. Potassium tetrachloromercurate (KTCM)
that western and eastern part of the study area are likely was used for sampling of SO2, and a mixed solution of
to be highly impacted, and south-western part of the sodium hydroxide and sodium arsenite was used for the
study area are likely to be moderately impacted by air sampling of NO2 as an absorbing solution. The sampling
pollutants. Considering these above facts from meteo- for both SO2 and NO2 were carried out for 04 h with an air
rological data and the previously described factors, six flow rate of 1.0 L/min, totalling to six samplings in 24 h
AAQ stations were selected (Table 3 and Fig. 4). (CPCB 2011). CO was analysed by digital CO analyser

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402 Page 6 of 17 Environ Monit Assess (2016) 188: 402

Fig. 3 Wind rose diagram of Sukinda Valley (December 2012 to November 2013)

(make: UNIPHOS, model no. 299). The sampling of CO humidity (RH), wind speed, wind direction and rainfall
was carried out for 1 h for each monitoring station. The during the study period were monitored using an Auto-
meteorological parameters, viz., temperature, relative matic Weather Monitoring Station (make: Virtual

Table 3 Ambient air quality monitoring stations

Sl. no. Station name Station code Geo-coordinates Direction of station wrt study area Type of area

1 Kalarangita A1 21° 00′ 31.40″ N 85° 44′ 10.58″ E South-west (SW) Commercial area
2 Chingudiapal A2 21° 02′ 31.38″ N 85° 45′ 35.84″ E West (W) Residential area
3 Sukurangi A3 21° 02′ 00.52″ N 85° 47′ 17.13″ E South (S) Residential area
4 Ostapal A4 21° 04′ 03.46″ N 85° 48′ 40.59″ E North (N) Residential area
5 Kansa A5 21° 01′ 13.27″ N 85° 52′ 03.56″ E East (E) Residential area
6 Kamarda A6 21° 03′ 24.24″ N 85° 51′ 0.96″ E East (E) Commercial area

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Environ Monit Assess (2016) 188: 402 Page 7 of 17 402

Fig. 4 Monitoring stations in the study area (Source: Google Earth 2014, imagery date 30 May 2010)

Hydromet). The methods followed for AAQ and meteo- overall pollutant concentration wrt the prescribed na-
rology monitoring are presented in Table 4. All the re- tional standards of pollutants and identifies the antici-
agents were prepared using metal-free analytical grade pated effect on health and environment. The API was
(Extra Pure) chemicals (Merck Millipore) for quality as- calculated by ‘average method’ following Ziauddin and
surance throughout the experiments and analyses. Double- Siddiqui (2006), using the formula as below:
distilled water prepared using a quartz distillation assembly
was used for preparing the reagents. Room temperature  
1 IPM10 IPM2:5 ISO2 INO2 ICO
was ∼30 °C while the analyses were carried out. All the API ¼  þ þ þ þ  100
5 SPM10 SPM2:5 SSO2 SNO2 SCO
polypropylene bottles and glassware were subjected to
cleaning procedures prescribed by Laxen and Harrison
(1981). where, IPM10, IPM2.5, ISO2, INO2 and ICO represent
the individual concentration of PM10, PM2.5, SO2, NO2
Air pollution index and CO, respectively. Similarly, SPM10, SPM2.5, SSO2,
SNO2 and SCO represent their respective values (24
API represents the status of the air environment in a hourly) in National Ambient Air Quality Standards
particular area at a given time. It is the measure of the (NAAQS) as prescribed by CPCB.

Table 4 Methods adopted and instruments used for the sampling of the AAQ and meteorological parameters

Sl. no Parameter Methods of analysis Sampling instrument/apparatus Reference

1 PM10 Gravimetric method Respirable dust sampler (Ecotech, AAS 217 BL) CPCB (2011)
2 PM2.5 Gravimetric method Fine particulate sampler (Ecotech, AAS 127) CPCB (2011)
3 SO2 Improved West and Gaeke method Gaseous attachment (Ecotech, AAS 109) CPCB (2011)
4 NO2 Modified Jacob and Hochheiser method
5 CO Sealed electrochemical sensor CO analyser (UNIPHOS, 299) BIS (2006)
6 Meteorology Sensor detection and digital display Automatic Weather Monitoring Station (Virtual Hydromet) –

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402 Page 8 of 17 Environ Monit Assess (2016) 188: 402

Table 5 Pollutant range in Sukinda Valley in comparison with the other chromite and iron ore mines throughout the globe

Air quality Present observation Comparison with the previous studies


parameters
Range Average Concentration Type of industry Location of mine Reference
± SD range

PM10 (μg/m3) 52–187 107 ± 22.5 32–124 Chromite mine Sukinda, Odisha, India IEP (2015)
10–131 Chromite mine Rusterburg, South Africa Kgabi et al. (2011)
32–69 Chromite mine Sukinda, India IBM (2013)
13–215 Chromite mine Rustenberg, South Africa Kgabi (2006)
3–9 Chromite mine Rustenberg, South Africa Karonga and Kgabi
(2009)
195–259 Iron Mine Dubuna, Keonjhar, Sahoo and Behera
Odisha, India (2013)
PM2.5 (μg/m3) 25–88 51.9 ± 12.2 16–26 Chromite mine Rustenberg, South Africa Karonga and Kgabi
(2009)
SO2 (μg/m3) 7.2–18.1 12.5 ± 1.9 BDL Chromite mine Sukinda, Odisha, India IEP (2015)
8.5–45.5 Iron and manganese mine Joda-Barbil, Odisha, India Das et al. (2003)
3.3–4.9 Iron mine Dubuna, Keonjhar, Sahoo and Behera
Odisha, India (2013)
NO2 (μg/m3) 16.4–34.2 25.4 ± 3.61 6.8–59.7 Chromite mine Sukinda, Odisha, India IEP (2015)
10.5–55.9 Iron and manganese mine Joda Barbil Odisha, India Das et al. (2003)
21.6–28.7 Iron mine Dubuna, Keonjhar, Sahoo and Behera
Odisha, India (2013)

Statistical analysis pollutants (SO2, NO2 and CO) varied significantly


among the AAQ monitoring stations (GLM-ANOVA,
The data as obtained for various AAQ and meteorological p < 0.05), whereas only NO2 varied significantly
parameters throughout the monitoring period were subject- within the months (GLM-ANOVA, p < 0.05).
ed to a suite of statistical tests for better interpretation and Many of the previous studies reveal that Sukinda
inference. To find the range and distribution of different Valley is impacted by Cr(VI) (Dhakate and Singh
parameters, basic descriptive statistics was performed. A 2008; Pattnaik and Panda 2011; Pattnaik et al.
two-tailed Pearson’s correlation test was performed to 2012; Mishra and Sahu 2013). Further, the present
understand the association between different AAQ param- findings substantiate the fact and reveal that the
eters and those with meteorological variables, which influ- region is also polluted by various air pollutants
ence the dispersion of various air pollutants, using (both particulate and gaseous pollutants). The con-
MEGASTAT 8.8 (Orris 2000). We conducted univariate centration of gaseous pollutants in the study area
test, general linear model ANOVA (GLM-ANOVA), to were low and within the prescribed limits, whereas
assess the variations in the AAQ parameters among the the concentration of particulate pollutants were
stations and months. All the statistical tests were performed above the prescribed limits of NAAQS (CPCB
at α = 0.05 level. These statistical tests were performed 2011). The levels of air pollutants were also com-
using SPSS 13.0 (Norusis 1990). pared with those reported earlier from other chro-
mite and ferrous mines to understand the prevail-
ing situation in Sukinda Valley (Table 5). This is
Results and discussion due to the fact that chromite contains higher per-
centage of Fe (IBM 2013). The details of the
The findings of the present study revealed that both the results obtained for each of the AAQ parameters
particulate pollutants (PM10 and PM2.5) and gaseous are described in the following sections.

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Environ Monit Assess (2016) 188: 402 Page 9 of 17 402

API AM ± SD
Particulate matter concentrations

46.6 ± 8.13

53.7 ± 10.3
44.1 ± 5.9
53.5 ± 8.6
56 ± 9.7
45.7 ± 8.7
The concentration of PM10 in the study area ranged from
52 μg/m3 (A4) to 187 μg/m3 (A6, Table 6). Though the
24 hourly concentration of PM10 exceeded in all the

493.2 ± 232.6
493.6 ± 232.6
287.2 ± 152.7
293.6 ± 163.4

391.5 ± 209.4
214.9 ± 117.9
AM ± SD monitoring stations, stations like A1, A3, A5 and A6
showed average six monthly concentrations above the
prescribed standards of NAAQ (100 μg/m3, CPCB
2011), i.e. 101.3, 114, 113.5 and 119.6 μg/m3, respec-
tively. Similarly, the concentration of PM2.5 ranged from
CO (μg/m3)

25 μg/m3 (station A4) to 88 μg/m3 (station A6). All the


100–800
100–900
100–600

100–500
100–600

100–800
Range

monitoring stations exceeded the prescribed standards


of NAAQ (60 μg/m3, CPCB 2011) except station A4,
where the reported maximum PM2.5 concentration was
26.7 ± 3.1
23.2 ± 2.1
27.3 ± 3.1
23.6 ± 3.9
24.4 ± 3.3
26.5 ± 3.6
AM ± SD

55 μg/m3. The concentration range of PM10 and PM2.5


in all the six monitoring stations along with their mean
and standard deviations are presented in Table 6. Similar
NO2 (μg/m3)

trends of PM concentration was found in several chro-


20.5–33.4
18.8–28.6
20.9–34.2
16.4–31.2
18.4–30.1
18.7–33.8

mite and iron mines (Kgabi 2006; Karonga and Kgabi


Range

2009; Kgabi et al. 2011; IBM 2013; Sahoo and Behera


2013; IEP 2015). Opencast mining contributed about
73 % of the total PM to the atmosphere (Sing and Pal
13.3 ± 1.7
11.9 ± 1.5
13.7 ± 1.6
11.3 ± 1.8
11.9 ± 1.8
12.9 ± 1.8
AM ± SD

2010).
GLM-ANOVA test revealed that the concentration of
PM10 and PM2.5 varied significantly within the sam-
SO2 (μg/m3)

pling stations (F 10.879, df 5, p < 0.05 for PM10 and F


9.2–17.3
9.5–18.1
7.2–16.5
8.5–14.5
8.3–15.5
8.6–15.5

12.645, df 5, p < 0.05 for PM2.5). This could be ascribed


Range

to the differences in the sampling stations especially


with respect to the landscape, proximity to the mine
Table 6 Concentrations of the monitored air pollutants in Sukinda Valley

site and the prevailing meteorological conditions of the


55 ± 10.6
56.9 ± 13.4
47.1 ± 11.6

58.8 ± 3.2
48.6 ± 9.5

area. Charron and Harrison (2005) during their study on


AM ± SD

44.8 ± 6

fine (PM2.5) and coarse (PM2.5–10) fraction of PM in


PM2.5 (μg/m3)

London highway area also supports this view. Further,


various mining and ancillary activities such as vehicular
movements in the area might have contributed to the
Range

32–88
33–82
25–55
38–73
34–73
28–73

reported higher levels of PM concentration. Similar


causative factors were also observed by Prusty (2012),
AM arithmetic mean, SD standard deviation

during an ambient air quality monitoring programme in


114 ± 23.6
96.5 ± 15.3

119.6 ± 23.8
97 ± 21.1
101.3 ± 19.4

113.5 ± 20
AM ± SD

lignite mines of Western Kachchh region, India. The


main source of PM in the opencast mines is the fugitive
dust and their lateral dispersion much beyond the mine
PM10 (μg/m3)

lease area. The primary source of fugitive dust in an


70–187
68–161

68–152
68–144
54–137

52–116

operational mining area includes the activities like over-


Range

burden removal, blasting, mineral haulage, mechanical


handling operations, stock piles and site restoration
(Appleton et al. 2006).
Station code

The concentration of PM may fluctuate in many of


the similar mining clusters, as it depends upon factors
A5
A6
A1
A2
A3
A4

like climatic conditions, meteorology, mining and

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402 Page 10 of 17 Environ Monit Assess (2016) 188: 402

ancillary activities. Though dust in the Sukinda Valley as drilling, blasting and combustion processes add NO2
mainly comprises of chromite particles, sometimes it to the atmosphere (Pandey et al. 2014). Along with the
also contains trace amounts of Cr(VI) which have ad- mining activities, large number of vehicles around the
verse impact on environment (Mishra and Sahu 2013). mine site and nearby villages might have contributed to
PM10 was highly correlated with PM2.5. Being the frac- the higher levels of NO2 as was observed in other
tion of PM10, PM2.5 is also high and showed higher opencast mining areas in the country (Prusty 2012). A
correlation (Table 8). Similar correlations were found number of Heavy Earth Moving Machineries (HEMMs)
in the mining areas of Northern European countries and other heavy vehicles emit considerable amount of
(Tecer et al. 2008). API was found to be highly corre- NO2 leading to elevated concentration. Since monsoon
lated with PM10 and PM2.5, which is indicative of the plays an important role in the seasonal variation in NO2
contribution of PM in API increment. concentrations over India (Ghude et al. 2008), we ex-
amined the seasonal pattern of NO2 in relation with
Gaseous pollutant concentrations temperature and RH. NO2 was positively correlated
(r = 0.220) with temperature and negatively correlated
The concentration of SO2 varied from 7.2 μg/m3 (station (r = −0.201) with RH (Table 8).
A3) to 18.1 μg/m3 (station A6, Table 6) and was well CO concentration varied significantly among the
within the NAAQS (80 μg/m3, CPCB 2011). Concen- sampling stations (GLM-ANOVA, F 15.30, df 5,
tration of SO2 was well within the prescribed standards p < 0.05) and was well below the limits of NAAQS
of NAAQ (80 μg/m3, CPCB 2011). The concentration (4000 μg/m3, 1 hourly, CPCB 2011). The concentration
of SO2 varied significantly among the stations (GLM- of CO varied from 100 μg/m3 (all stations) to 900 μg/m3
ANOVA, F 14.542, df 5, p < 0.05) and months (GLM- (station A6, Table 6). The average value of CO varied
ANOVA, F 2.279, df 5, p < 0.05). Significant variation from 214.9 μg/m3 (station A4) to 493.6 μg/m3 (station
of SO2 among the stations is indicative of the occurrence A6). The unequal distribution of the sources of CO
of discrete mining and allied activities and the proximity emission, such as mining and vehicular activities, might
of the sampling stations to the mine site. Further, several have contributed to the observed variability of CO level
factors such as temperature inversions, changing wind in the area, and thus, PM10 and PM2.5 were significantly
patterns, landscape features and topography of the area correlated (positively) with CO (Table 8). This may be
in a valley might be a factor in restricting the dispersion due to the increment of vehicular activities in the mining
of the gases. Prusty (2012) also ascribes the temperature areas, which might have simultaneously exceeded the
inversion and mixing height in the lower atmosphere in concentration of PM along with CO. Vehicular emission
reducing the dispersion of pollutants, thereby increasing contributes considerably to the CO concentrations
the concentration of gases in and around the mining (Katiyar et al. 2003; Madhuri et al. 2003). As the major
sites. Wind speed, air masses and height of mixing layer transportation in the area is through HEMM and other
can also govern SO2 concentration (Pio and Feliciano heavy transporting vehicles, a significant generation of
1996). Processes such as advective inversion might play CO was expected. Sarmah et al. (2012) also of the view
a significant role in reduced dispersion of gaseous pol- that the mining activity alone does not cause the emis-
lutants in Sukinda Valley, which is predominantly land- sion of toxic gases but other collateral activities such as
locked by hillocks. burning of fuel and waste materials from mining have
The observed spatial (F 13.964, df 5, p < 0.05) and also greater influence on SO2, NO2 and CO concentra-
temporal (F 5.673, df 5, p < 0.05) variation in the NO2 tions (Fig. 4).
concentration in the area was significant (GLM-
ANOVA). The observed range for NO2 was between Air pollution index
16.4 μg/m3 (station A1) and 33.8 μg/m3 (station A3,
Table 6). The concentration of NO2 in all the monitoring The API being an indicative parameter of overall air
stations throughout the sampling period was well below quality of the area revealed that the area is under light to
the prescribed values of NAAQS (80 μg/m3, CPCB moderate air pollution with an API score of 25–75. The
2011). The observed variation in NO2 might be due to six monthly average API values varied from 44.1 (sta-
the variation in mining and transportation activities in tion A4) to 56 (station A6, Table 6), with the order of the
each monitoring station in the valley. The activities such stations as A6 > A3 > A5 > A1 > A2 > A4. Station A6

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Environ Monit Assess (2016) 188: 402 Page 11 of 17 402

a December 2013 b January 2014

c February 2014 d March 2014

e April 2014 f Ma y 2014


Fig. 5 a–f Monthly wind rose diagram (December 2013 to May 2014)

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402 Page 12 of 17 Environ Monit Assess (2016) 188: 402

Table 7 Meteorological parameters of the study area

Sl. no. Parameters December January February March April May


2013 2014 2014 2014 2014 2014

1 Temperature (°C) Range 12.11–31.3 12.79–30.73 12.26–30.75 16.86–41.87 20.78–44.59 24.63–44.87


Average ± SD 20.49 ± 5.6 21.31 ± 4.9 23.76 ± 5.6 27.93 ± 5.7 32.23 ± 5.8 32.60 ± 5.2
2 Relative humidity Range 26.35–96.68 31.09–96.26 17.63–97.65 16.2–97.2 10.25–97.17 12.83–98.17
(%) Average ± SD 72.11 ± 21.1 72.20 ± 18.6 64.13 ± 21.5 64.84 ± 21.6 54.61 ± 22.5 62.27 ± 22.2
3 Wind speed (m/s) Range 0–6.1 0–4.9 0–7.5 0–12.3 0–14.6 0–17.6
Average ± SD 1.1 ± 1 1.2 ± 1.1 1.8 ± 1.5 2±2 2.5 ± 2 2.5 ± 2
5 Rainfall (mm) Monthly total 0 0 11.6 23.4 1.4 62.6
No. of rainy days 0 0 1 9 4 10

was the highest polluted site of Sukinda Valley consid- during the monitoring period from W and NE (Fig. 5a–f)
ering API. Three of the monitoring stations (A3, A5 and could have also led to the increment of the pollutant
A6) were within the range of moderate air pollution, concentrations at stations A3, A5 and A6, which are
whereas the other three (A1, A2 and A4) of the moni- located in the E and SW direction with respect to the
toring stations were in the range of light air pollution mine area.
(Fig. 8). The daily air pollution index of the study area
showed that the area was within moderate to high air Meteorological condition of the study area
pollution (API 50–100). Stations A3 and A6 were with-
in the range of heavy air pollution (API 75–100) con- An analysis of the meteorological information
sidering the daily air pollution index (Fig. 8). The gen- (Table 7) reveals that both cold winter and hot
eral API level below 50 means that all pollutant levels summer were experienced in the study area. The
are in the satisfactory range over a 24-h monitoring pollution load depends upon the emission levels
period and from 50 to 100 indicates the pollutants are from different sources, the locations and height
at high level (Wang and Wei-Zhen 2006). As previously of emission sources and micrometeorological fac-
discussed, API is highly correlated with PM10 and tors (Prusty et al. 2005). The temperature varied
PM2.5. Similar results were also found by Pandey et al. from 12.11 to 44.87 °C and increased significantly
(2014). The higher concentrations of pollutants in sta- from December 2013 through May 2014. Higher
tions A3, A5 and A6 could be ascribed to their proxim- temperature of the area can play a significant role
ity to the mine site. The predominant wind direction in the dispersion of particulate as well as gaseous

Table 8 Correlation matrix of air quality parameters and meteorological variables

PM10 PM2.5 SO2 NO2 CO API WS TEMP RH

PM10 1.000
PM2.5 0.946** 1.000
SO2 0.388** 0.403** 1.000
**
NO2 0.469 0.459** 0.463** 1.000
** **
CO 0.523 0.538 0.383** 0.411** 1.000
** ** **
API 0.975 0.974 0.481 0.567** 0.631** 1.000
WS 0.107 0.096 0.113 0.220 **
−0.090 0.106 1.000
TEMP 0.020 0.031 0.111 0.160** −0.183** 0.023 0.662** 1.000
RH −0.189 **
−0.162 **
−0.099 −0.201 **
0.022 −0.175**
−0.510** −0.643** 1.000

282 sample size


** ± 0.153 critical value 0.01 (two-tail), * ± 0.117 critical value 0.05 (two-tail)

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Environ Monit Assess (2016) 188: 402 Page 13 of 17 402

pollutants. Temperature and PM have a significant pollutants except CO (Table 8). The lower RH along
effect on the occurrence of episodic events (Tecer with high wind speed may lead to the dispersion of
et al. 2008). Being a valley, during the daytime, pollutants in and around the mining area. The increment
and in the active hours of the mining, the air near of RH plays a significant role in increase in the episodic
the mountain slope warms up faster than the air at value of PM10 and PM2.5. Further, the cloud scavenging
the same altitude but away from the mountain. characteristics of RH levels (>83 %) might result in low
This can cause a local pressure gradient, and air concentration of gases and aerosols (Elminir 2005). In
is forced to flow up the mountain slope as moun- addition, mining and allied activities during the peak
tain breeze, which can be a major factor for the hours could also be responsible for the increase in
dispersion of the particulate pollutants (Rao 1991). episodic values of PM.
The RH varied from 10.25 to 98.17 %, and the The total rainfall (62.6 mm) and the number of rainy
average RH was higher in winter days than summer. days (10) were highest in May 2014. There was no rain
The RH was negatively correlated with all the examined during the winter months, i.e. during December 2013 and

a A1 b A2

c A3 d A4

e A5 f A6

Fig. 6 a–f Correlation between wind direction and PM10

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402 Page 14 of 17 Environ Monit Assess (2016) 188: 402

Fig. 7 Temporal variation of


PM10 concentrations
120

PM10 Concentrations ()µg/m3)


100

Dec-13
80
Jan-14
Feb-14
60
Mar-14
Apr-14
40
May-14

20

0
A1 A2 A3 A4 A5 A6
AAQ Sampling Stations

January 2014. Though no monitoring was done during the frequent dust storm and hazy conditions which
rainy days, it can have an impact on the suppression and build up high PM levels in the ambient air. The
washout of air pollutants (Tecer et al. 2008). Under the influence of meteorological parameters on PM is
condition of low rainfall, PM concentration in ambient air discussed in the subsequent sections. Wind speed
tends to increase (Larssen et al. 2007). was significantly correlated with temperature
The highest wind speed in the study area was (r = 0.662) and RH (r = −0.510, two-tailed
17.6 m/s. The average wind speed increased from Pearson’s correlation test, Table8). This might be
December 2013 through May 2014. The decrease due to the temperature inversion phenomena (Rao
in RH and increase in the wind speed could be a 1991), as previously described.
major cause for the dispersion of pollutants. The
results of PM10 revealed that wind speed higher Correlation between wind direction and PM10
than 2.80 m/s decreased the episodic days up to concentrations
40 % (Tecer et al. 2008). Prakash and Bassin
(2010) observed that strong and medium winds Wind direction was one of the major factors for the
during April to June create turbulent conditions dispersion of air pollutants from their source of gener-
and local disturbances in the environment causing ation. Sukinda Valley is surrounded in the north and

Fig. 8 Daily air pollution index


(monthly average) in the study
area (X-axis represents the
stations A1–A6)

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Environ Monit Assess (2016) 188: 402 Page 15 of 17 402

south, by hill stations (Daitari and Mahagiri hills). Conclusion


Thus, the predominant wind direction was from E
and from W. In the present study, wind direction was The present study at Sukinda Valley revealed that the
from W during the months of December 2013 through operation of the opencast chromite mine has significant
March 2014 (Fig. 5a–f). During the months of April impact on the residential and commercial areas in the
and May 2014, the wind direction was reversed and buffer zone. The area is highly polluted with coarse
was from E and NE direction. Stations A3, A5 and A6 (PM10) and fine (PM2.5) fraction of particulate matters.
were highly impacted which could be ascribed to The ongoing mining activities without proper environ-
these reasons. SPM is known to be strongly associat- mental management strategies seemed to have caused
ed with the predominant wind direction of a particular the degradation of the surrounding environment.
area (Poykio et al. 2002; Tecer et al. 2008), which was
closely observed during the present study. Most of the (i) Particulate matter concentrations were above the pre-
monitoring stations were significantly impacted by scribed limits of NAAQS indicating the said area to
wind direction. PM10 concentration was highest when be polluted. However, the concentrations of the gas-
the wind direction was either from east or west direc- eous pollutants, viz., SO2, NO2 and CO were well
tion, due to the geographical position of the valley. within the prescribed standards of NAAQ. Sukurangi
Thus, the stations present in the W (station A1 and (residential), Kansa (residential) and Kamarda
station A2) and in the E (station A5 and station A6) (commercial) stations were highly impacted with PM.
were highly impacted (Fig. 6a–f). Though the stations (ii) The API is suggestive of the area to be in light to
A1 and A2 were impacted throughout the sampling moderately polluted category considering the half
period, they seemed to be highly impacted when the yearly average value. Daily API indicated the area
wind direction was from eastern quadrant (45° to in the zone of moderate to high air pollution and
135°) of the study area, i.e. during the months of April Sukurangi (residential), Kansa (residential) and
and May 2014 (Fig. 6a–f). Kamarda (commercial) stations fall under highly
Similarly, during the months of February 2014– polluted zone.
May 2014, though the predominant wind direction (iii) API was highly correlated with the particulate
was from W and E, wind direction was also ob- matter indicating its higher contribution in the
served from NE quadrant. This may be a major score.
cause for the higher dust concentration at station (iv) The role of meteorological variables, viz., temper-
A3, which is located in the SW direction of the ature, relative humidity, wind speed and wind di-
study area (Fig. 4). Similarly, stations A5 and A6 rection in dispersing the particulate matter was
are in the E of the study area and had higher evident. Wind speed and temperature in association
concentrations of PM during the months of Decem- with wind direction seemed to be responsible for
ber 2013 to March 2014 (Fig. 7), wherein the wind dispersion of particulate matters from their source
direction was from the west (Fig. 5a–f). Station A4 of generation to the receptor points, i.e. the sur-
did not show any relation between wind direction rounding residential and commercial areas.
and PM10 throughout the sampling period, which (v) Proper mitigation measures and pollution control
may be due to its location, in the north (N) direction strategies should be followed by the mining lessees
of the study area. Further the wind direction was of Sukinda Valley to control the particulate matters.
least observed from the southern quadrant throughout Appropriate water sprinkling in the haul and trans-
the monitoring period. Poykio et al. (2002) observed portation roads under supervision and by specially
the impact of wind direction on PM around chromite designed tankers (rear water sprays) should be prac-
mines from heap of mining spoil, enrichment plants, tised. Auto sprinklers on both sides of the road can be
railway line, etc. The presence of discrete mining used for more effective sprinkling. Wet drilling sys-
overburden dumps, transportation roads, crushing tems should be developed instead of dry drilling
and enrichment plants were the major source of process, which suppresses the dust particles generat-
PM in mining areas. These particulates were ed during drilling. The use of wet spray system (dry
transported by wind and seemed to affect the nearby fog) should be incorporated in the major dust emit-
residential areas as per the wind patterns (Fig. 8). ting activities such as crushing and screening.

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402 Page 16 of 17 Environ Monit Assess (2016) 188: 402

Acknowledgments We are thankful to Mr. Dayananda Pandey, Dhal, B., Das, N. N., Pandey, B. D., & Thatoi, H. N. (2010).
Managing Director, M/s Ecological Development Consultancy Environmental quality of Boula-Nuasahi chromite mine area
Pvt. Ltd., Bhubaneswar, Odisha, for providing the sampling and in India. Mine Water and the Environment, 30, 191–196.
analysis facilities to Mr. S. R. Mishra to carry out the work. We are Elminir, H. K. (2005). Dependence of urban air pollutants on
also thankful to Dr. Rachna Chandra, Senior Scientist in Terrestrial meteorology. Science of the Total Environment, 350, 225–
Ecology Division of Gujarat Institute of Desert Ecology for her 237.
guidance and suggestions during the data analysis and preparation Ghude, S. D., Fadnavis, S., Beig, G., Polade, S. D., & Van der A.,
of manuscript. R. J. (2008). Detection of surface emission hot spots, trends,
and seasonal cycle from satellite-retrieved NO2 over India.
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