ABSTRACT- To evaluate the susceptibility of plants growing in the industrial area of Tarapur, Maharashtra, Air
pollution tolerance index (APTI) was determined for 30 plants species by calculating Ascorbic acid content, Leaf-extract
pH, Total chlorophyll content and Relative water content and computing together in a formula. The result showed the
order of tolerant species as Putranjiva roxburghii >Mangifera indica >Ficus racemosa >Ficus hispida >Morinda citrifolia
and the order of sensitive species as Nyctanthes arbor-tristis >Bauhinia purpurea> Peltophorum pterocarpum>Psidium
guajava> Morinda pubescens. Air pollution tolerance index (APTI) serves as a reliable technique in qualifying plants as
tolerant and sensitive species in regard to air pollution. Tolerant species serve as sink of air pollutants and thus can help in
abatement of air pollutants to some extent if planted in and around industrial vicinity and along traffic islands.
Key-words- Air pollution tolerance index (APTI), Ascorbic acid content, Leaf-extract pH, Total Chlorophyll Content,
Relative Water Content
1. INTRODUCTION
Today the most important topic of global concern is
pollution. With rising industrialization and development, an
increase in degradation of environment is faced all over the
world. Air pollution is one of most fatal of all as we can’t
cease the air we breathe. The three main sources of air
pollution problem in India are vehicles, industries and
domestic sources. As per the guidelines of Ambient air
quality monitoring by Central pollution control board,[1] the
reasons for high air pollution in India are: poor quality of
fuel, poor vehicular design, uncontrolled expansion of
vehicle population, old process technology in industries,
wrong location of industries, no pollution preventive step in
early stage of industrialization,
no pollution prevention or control system and poor
compliance of standard in small/medium scale industries.
Air pollution affects the plants as much as it affects humans
and animals. On exposure to air borne pollutants, plants
experience physiological changes before showing visible
damage to leaves [2]. Some plants can thrive in polluted
environment and can thus help in cleaning the various
sources of manmade pollution both organic (petrochemical)
and inorganic (heavy metal toxins) [3]. As part of their
regular functioning, trees remove significant amount of
pollution from the environment, increasing the air quality
and thus should be considered an integral part in aiming
overall air quality [4]. The response of plants to pollutants at
physiological and biochemical level can be understood by
analyzing the factors that determine sensitivity and
tolerance.[5] [6] Rao suggested a method where four
biochemical parameters such as Ascorbic acid, Total
chlorophyll content, Leaf-extract pH and Relative water
content were used in determining the resistance and
susceptibility of plants to air pollution. Plants with higher
APTI value are more accomplished to combat against air
pollution and can be used to mitigate pollution, while those
with low index value show less tolerance and can be used
to signify levels of air pollution. [7]
2. MATERIALS AND METHOD
2.1 Study Area:
Tarapur industrial area was established
in Palghar Taluka of Thane district, Maharashtra by
Government of India in 1972. Also known as MIDC
Tarapur, it is one of the largest chemical industrial estates
of Maharashtra. Tarapur is located 100 km away from
Mumbai on western railway track and Boisar is the nearest
railway station. It houses many industries like 392 dye
industries, 265 textile industries, 138 engineering, 26 iron
and steel industries and 1 pesticide industry which are
considered as the highly polluting industries by
Maharashtra Pollution Control Board [8]. CPCB [9] based on
the Comprehensive Environmental Pollution Index (CEPI
Index) declared 43 critically polluted areas in India. CEPI
Index for Tarapur was 60.75 indicating high pollution
levels and hence this area was considered for the
experimental study. The location of study site is given in
Fig 1.
2.2 Sampling of plant species:
Fully matured leaves
samples were collected from 30 plant species found in this
industrial area during two dry seasons i.e. summer and
winter (2014). The leaves were brought to laboratory with
care, were washed with distilled water to get rid of dust
particles and fresh weight was taken immediately. Fresh
leaf samples were then analyzed for Ascorbic acid, [10]
Leaf-extract pH. [11] Total chlorophyll, [12] and Relative
water content. [13]
2.3 Analysis:
2.3.1 Ascorbic acid determination:
A homogenate was
prepared using fresh leaf of the concerned tree species and
oxalic acid which was later reacted with 2, 4–Dinitrophenyl
hydrazine reagent along with Sulphuric acid to give an
orange red color solution. The absorbance was measured at
540nm.
2.3.2 Leaf-extract pH:
1 gm fresh leaf of the concerned
tree species was homogenized using distilled water and pH
of the filtrate was detected using digital pH meter.
2.3.3 Total chlorophyll content:
Chlorophyll content
was analyzed by homogenizing 1gm leaf sample in 20 ml
pre-chilled acetone and centrifuging at 5000rpm. The
supernatant was later collected and absorbance was
measured at 645 and 663nm.
2.3.4 Relative water content:
Relative water was
calculated by taking fresh weight, dry weight and turgid
weight of leaf samples and substituting them in the
following formula:
(FW – DW)
RWC = ------------------------x 100
(TW– DW)
Where,
FW- Fresh weight, DW- Dry weight and TW- Turgid
weight
2.3.5 Air Pollution Tolerance Index (APTI):
The values
of all the above parameters where then incorporated in
the equation as suggested by Singh and Rao
[6] and the Air
Pollution Tolerance Index for plants was calculated using
the formula:
A (T+P) +R
APTI = ----------------------
10
Where, A =Ascorbic Acid (mg/g),
T =Total Chlorophyll
(mg/g),
P = pH of the leaf extract and
R = Relative water
content of leaf (%).
2.4 Statistical Analysis:
Data was analyzed using Correlation and Linear regression
analysis between independent variables i.e. ascorbic acid,
total chlorophyll, pH, relative water content and dependant
variable like A.P.T.I.
                         
Fig 1: Location of study site – Tarapur M.I.D.C.
Table 1: General description of the plant species considered for APTI study
S.No | Plant species name | Family | Sub-family |
Common
name | Tree type |
1 | Acacia auriculiformis Benth | Leguminosae | Mimosaceae |
Australian babul |
Evergreen |
2 | Albizia saman (Jacq.) Merr. | Leguminosae | Mimosaceae | Rain tree | Deciduous |
3 | Alstonia scholaris (L.) R. Br. | Apocynaceae | – | Saptaparni | Evergreen |
4 | Annona squamosa L. | Annonaceae | – | Custard apple | Deciduous |
5 | Artocarpus heterophyllus Lam. | Moraceae | – | Jackfruit | Evergreen |
6 | Azadirachta indica A. Juss. | Meliaceae | – | Neem | Evergreen |
7 | Bauhinia purpurea L. | Leguminosae | Caesalpiniaceae | Apta | Deciduous |
8 | Butea monosperma (Lam.) Taub. | Leguminosae | Caesalpiniaceae |
Palas, Flame
of forest |
Deciduous |
9 | Cassia fistula L. | Leguminosae | Caesalpiniaceae |
Indian laburnum |
Deciduous |
10 | Delonix regia (Boj. ex. Hook.) Raf | Leguminosae | Caesalpiniaceae | Gulmohar | Deciduous |
11 | Ficus benghalensis L. | Moraceae | – | Banyan | Evergreen |
12 | Ficus hispida L. | Moraceae | – | Benjamin tree | Evergreen |
13 | Ficus racemosa L. | Moraceae | – | Umbar | Evergreen |
14 | Ficus religiosa L. | Moraceae | – | Pipal | Evergreen |
15 | Gardenia jasminoides J.Ellis | Rubiaceae | – | Anant | Evergreen |
16 | Gliricidia sepium (Jacq.) Kunth ex Walp. | Leguminosae | Fabaceae | Giripushpa | Deciduous |
17 | Lagerstroemia speciosa (L.) Pers | Lythraceae | – | Taman | Deciduous |
18 | Mangifera indica L. | Anacardiaceae | – | Mango | Evergreen |
19 | Morinda citrifolia L. | Rubiaceae | – | Noni | Evergreen |
20 | Morinda pubescensJ. E. Sm. | Rubiaceae | – | Bartondi | Evergreen |
21 | Nyctanthes arbor-tristis L. | Oleaceae | – | Parijatak | Evergreen |
22 | Peltophorum pterocarpum (DC.) K.Heyne | Leguminosae | Caesalpiniaceae |
Copper pod
tree |
Evergreen |
23 | Plumeria obtusa L. | Apocynaceae | – | Chafa | Evergreen |
24 | Polyalthia longifolia Sonn. | Annonaceae | – | False Asoka | Evergreen |
25 | Pongamia pinnata (L.) Pierre | Leguminosae | Fabaceae | Karanj | Deciduous |
26 | Psidium guajava L. | Myrtaceae | – | Guava | Evergreen |
27 | Putranjiva roxburghii Wall. | Putranjivaceae | – | Putranjiva | Evergreen |
28 |
Senna siamea (Lam.) H.S. Irwin & Barneby |
Leguminosae | Caesalpiniaceae | Kashid | Evergreen |
29 | Syzygium cumini (L.) Skeels | Myrtaceae | – | Jamun | Evergreen |
30 | Tamarindus indica L. | Leguminosae | Caesalpiniaceae | Imli | Evergreen |
Table 2: Air pollution tolerance index of trees from industrial area of Tarapur (Average of biochemical parameters
from summer and winter season± SD)
S. No | Plant species name |
Ascorbic acid
content |
Total chlorophyll
content |
pH |
Relative water
content |
APTI |
1 | Acacia auriculiformis | 0.64±0.04 | 0.39±0.03 | 6.44±0.54 | 85.01±1.91 | 8.93±0.13 |
2 | Albizia saman | 0.48±0.09 | 0.74±0.25 | 6.43±0.13 | 67.06±2.34 | 7.05±1.16 |
3 | Alstonia scholaris | 0.88±0.25 | 0.78±0.02 | 5.94±0.01 | 82.11±2.66 | 8.80±0.44 |
4 | Annona squamosa | 0.31±0.02 | 0.40±0.09 | 5.53±0.72 | 73.44±1.00 | 7.53±0.07 |
5 | Artocarpus heterophyllus | 0.54±0.09 | 0.45±0.11 | 6.58±0.07 | 71.72±1.30 | 7.55±0.64 |
6 | Azadirachta indica | 1.39±0.02 | 0.41±0.05 | 6.21±0.13 | 73.56±2.56 | 8.27±0.26 |
7 | Bauhinia purpurea | 0.47±0.17 | 0.39±0.02 | 4.82±2.57 | 66.75±2.00 | 6.92±0.82 |
8 | Butea monosperma | 0.64±0.05 | 0.42±0.13 | 6.42±0.27 | 78.94±1.85 | 8.33±0.23 |
9 | Cassia fistula | 1.55±0.05 | 0.67±0.02 | 6.79±0.45 | 78.50±3.17 | 9.00±0.72 |
10 | Delonix regia | 0.21±0.04 | 0.40±0.24 | 6.83±0.13 | 74.06±2.22 | 7.56±1.31 |
11 | Ficus benghalensis | 0.58±0.05 | 0.36±0.01 | 6.18±0.91 | 87.96±3.21 | 9.17±0.21 |
12 | Ficus hispida | 0.49±0.04 | 0.55±0.15 | 5.75±0.91 | 90.08±3.37 | 9.31±0.67 |
13 | Ficus racemosa | 0.97±0.03 | 0.37±0.01 | 5.55±0.45 | 92.87±3.01 | 9.86±0.20 |
14 | Ficus religiosa | 0.51±0.04 | 0.69±0.01 | 5.88±0.91 | 80.21±0.65 | 8.36±0.67 |
15 | Gardenia jasminoides | 0.61±0.06 | 0.43±0.47 | 6.27±0.13 | 76.17±2.44 | 8.02±0.47 |
16 | Gliricidia sepium | 0.91±0.03 | 0.33±0.08 | 6.23±0.15 | 64.75±1.71 | 7.07±1.94 |
17 | Lagerstroemia speciosa | 0.97±0.15 | 0.31±0.04 | 5.59±0.13 | 71.38±1.60 | 7.71±0.85 |
18 | Mangifera indica | 1.49±0.41 | 0.51±0.01 | 6.47±0.31 | 89.88±1.17 | 10.03±1.44 |
19 | Morinda citrifolia | 1.30±0.01 | 0.70±0.16 | 6.31±0.06 | 83.53±3.13 | 9.26±0.30 |
20 | Morinda pubescens | 1.47±0.56 | 0.64±0.06 | 5.97±0.62 | 60.32±3.06 | 7.00±2.00 |
21 | Nyctanthes arbor-tristis | 0.64±0.06 | 0.50±0.04 | 6.38±0.04 | 64.25±0.25 | 6.87±0.02 |
22 | Peltophorum pterocarpum | 0.33±0.04 | 0.70±0.01 | 6.29±0.28 | 67.40±3.08 | 6.97±0.60 |
23 | Plumeria obtusa | 0.60±0.03 | 0.58±0.18 | 5.89±0.14 | 83.62±3.13 | 8.75±0.53 |
24 | Polyalthia longifolia | 0.20±0.01 | 0.42±0.03 | 6.68±0.11 | 89.69±1.83 | 9.11±0.26 |
25 | Pongamia pinnata | 1.59±0.37 | 0.58±0.35 | 6.92±0.08 | 80.01±2.99 | 9.19±0.27 |
26 | Psidium guajava | 1.56±0.01 | 0.30±0.01 | 6.45±0.21 | 59.48±2.43 | 7.00±0.23 |
27 | Putranjiva roxburghii | 8.35±0.19 | 0.53±0.06 | 6.25±0.13 | 91.97±2.70 | 14.85±0.45 |
28 | Senna siamea | 0.64±0.31 | 0.65±0.06 | 5.65±0.28 | 78.55±3.29 | 8.26±0.53 |
29 | Syzygium cumini | 0.45±0.09 | 0.34±0.15 | 6.23±0.14 | 77.95±1.81 | 8.09±1.74 |
30 | Tamarindus indica | 0.44±0.01 | 0.38±0.01 | 3.63±0.04 | 81.64±2.62 | 8.34±0.47 |
Table 3: Correlation between different biochemical parameters and APTI values
| Ascorbic acid content |
Total chlorophyll
content |
pH | Relative water
content |
APTI |
Ascorbic acid content | 1 | | | | |
Total chlorophyll content | 0.075 1 | | | | |
pH | 0.122 | 0.174 | 1 | | |
Relative water content | 0.246 | 0.058 | -0.030 | 1 | |
APTI | 0.800 | 0.094 | 0.080 | 0.777 | 1 |
Fig. 2: Linear regression analysis between APTI and Ascorbic acid content
Fig. 3: Linear regression analysis between APTI and pH
Fig. 4: Linear regression analysis between APTI and Total chlorophyll content
Fig. 5: Linear regression analysis between APTI and relative water content
Fig. 6: APTI of plant species from industrial area of Tarapur
3. RESULTS AND DISCUSSION
Most of the plant species selected for the study showed
higher APTI in winter as compared to summer season. The
average value of summer and winter season was evaluated
for all the biochemical parameters and then substituted in
APTI formula to give an average APTI for all the plant
species considered for the study (Table 2, Fig. 6). This
helped in identifying the tolerant and sensitive nature of
plant species towards pollution.
3.1 Ascorbic acid content:
Ascorbic acid showed a
weak positive correlation with Total chlorophyll content
(r=0.075), pH (r=0.122) and relative water content
(r= 0.246) but had a strong positive correlation with APTI
(r=0.80) of plant species (Table 3). P
utranjiva roxburghii
(8.35mg/g) showed high ascorbic acid content while lowest
ascorbic acid was seen in
Polyalthia longifolia (0.2mg/g)
(Table 2). Being a natural antioxidant, Ascorbic acid plays
an important role in pollution tolerance by activating many
physiological and defense mechanism in plants.
[13] According
to Garg
[14] boost in the level of ascorbic acid content
may be due to the resistance mechanism of plant to cope
with stress condition since it slows down the leaf
senescence. Thus
Putranjiva shows tolerance nature to air
pollutants while Polyalthia shows stive nature.
3.2 Leaf-extract pH: A negative correlation (r= -0.030)
was seen between pH and relative water content and weak
correlation existed between pH and APTI value (r=0.080)
(Table: 3). Highest value for pH was seen in Pongamia
pinnata (6.92) while lowest pH value was seen in
Tamarindus indica (3.63) (Table 2). Agarwal [15] stated that
low pH decreases the efficiency of hexose sugar conversion
to ascorbic acid and the reducing activity of Ascorbic acid
is more at higher pH than at lower pH. Thus high pH can
provide tolerance to plants against pollutants. Hence we
can say that Pongamia is tolerant species while Tamarindus
is sensitive species.
3.3 Total chlorophyll content:
Total chlorophyll
depicted a weak positive correlation with pH (r=0.174),
relative water content (r=0.058) and APTI (r=0.094) (Table:
3).
Alstonia scholaris (0.78mg/g) showed high total
chlorophyll content, thus showing sensitivity to pollution
while lowest chlorophyll content was seen in
Psidium
guajava (0.3mg/g) thus showing tolerance behavior. Joshi
[16] concluded in their research that the most important
photoreceptor in photosynthesis is Chlorophyll and its
measurement is a significant tool to calculate the effects of
air pollutants on plants as it plays a crucial role in plant
metabolism; any reduction in chlorophyll content directly
affects the plant growth. Total chlorophyll content of all the
plant samples was less than 1mg/g. Das
[17] suggested that
high dust accumulation during the winter may be due to
wet leave surface with foggy condition and gentle breeze
which prevents particle dispersion; and low dust accumulation
in summer may be due to high wind speed. Low
chlorophyll content during winter season may be due to
high dust accumulation on foliar surface of plants inhibiting
photosynthesis due to presence of various metals and
particles.
3.4 Relative water content:
A strong positive correlation
(r=0.777) exists between relative water content and
APTI of plant species (Table: 3).
Ficus glomerata (92.87%)
showed high relative water content while lowest was seen
in
Psidium guajava (59.48%). Relative water content is the
water content of leaf which helps in maintaining the
physiological balance in plant body under stress conditions
induced by air pollution.
[18] High Relative water content
would mean tolerance to pollutants.
3.5 Air pollution tolerance index of plants:
By
evaluating all the four biochemical parameters in the
equation of APTI given by Singh and Rao,
[17] Air pollution
tolerance index of plants was calculated for 30 plants
species and is depicted in Table 2. The tolerant plant
species were
Putranjiva roxburghii, Mangifera indica,
Ficus glomerata, Ficus benjamina and Morinda citrifolia
while the sensitive species were
Nyctanthes arbor-tristis,
Peltophorum pterocarpum, Bauhinia purpurea, Psidium
guajava and Pithecolobium saman (Fig. 6). Regression
analysis as shown in Fig. 2, 3, 4 and 5 revealed that
Ascorbic acid content and Relative water content were
positively correlated with APTI value while Leaf extract
pH and total chlorophyll content showed a lesser
correlation with APTI of the plant species. This means that
both Ascorbic acid content and Relative water content are
reliable parameters for checking the susceptibility of plant
species.
4. CONCLUSIONS
Air pollution tolerance index (A.P.T.I.) study proves
significant in determining the tolerant and sensitive nature
of plant species in environment. Higher the A.P.T.I. value
more is the tolerance of the plant species and lesser the
APTI value, more is the sensitivity of the plant species.
Among 30 plant species considered for the experimental
study, the order of plants tolerant to air pollution can be
stated as
Putranjiva roxburghii>Mangifera indica>Ficus
racemosa>Ficus hispida>Morinda citrifolia> Pongamia
pinnata>Ficus benghalensis> Polyalthia longifolia>
Cassia fistula> Acacia auriculiformis. Tolerant plant
species can be used in green belt development as they tend
to serve as barriers and act as sink for air pollutants. These
can thus be planted in and around industrial vicinity and
traffic islands to control the level of air pollution. The order
of sensitive plant species can be given as
Nyctanthes
arbor-tristis>Bauhinia purpurea> Peltophorum pterocarpum>
Psidium guajava> Morinda pubescens> Albizia
saman> Gliricidia sepium> Annona squamosa>
Artocarpus heterophyllus> Delonix regia. Sensitive plant
species on the other hand act as Bioindicators of air
pollution and thus can be planted in order to check the
environmental health from time to time. High pollution
levels can lead to deforestation in long run and thus this
kind of study helps in understanding the plants susceptibility
and resistance to pollution loads.
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