Results and Discussion
Ichthyofauna Diversity of Lakes
The present study records 18 species of ichthyofauna belonging to
4 orders, 7 families and 14 genera (Figure 9.2). The
ichthyofauna belonging to order (Figure 9.3a) Cypriniformes were
dominant in lakes (41 per cent) followed by Perciformes (33 per
cent), Cyprinodontiformes (15 per cent) and Siluriformes (11 per
cent).
The order Cypriniformes consists of species namely Catla
catla, Labeo rohita, Ctenopharyngodon
idella, Cyprinus carpio, Cirrhinus
mrigala, Labeo fimbriatus, Puntius ticto and
Hypophthalmichthys molitrix. Cyprinodontiformeswas
represented by species such as Gambusia affinis and
Poecilia reticulata. Perciformes was represented by
Oreochromis mossambicus, Oreochromis niloticus,
Channa punctata, Channa striata and Parambassis
ranga. Siluriformeswas represented by Clarias
gariepinus, Clarias batrachus and Heteropneustes
fossilis. Similar results were observed in other lakes, for example, the order Cypriniformes
were dominant in Mallasandralake of Tumakuru (Nayaka, 2018);
Kelagerilake of Dharwad (Kamble and Ganesh, 2016) and Nagaram
tank (Ramulu and Benarjee, 2013).
Figure 9.2: Distribution of Ichthyofauna (Order wise and
family wise) in Lakes of Bangalore.Fish species
belonged to 7 families (Figure 9.3b) namely, Ambassidae, Channidae,
Cichlidae, Clariidae, Cyprinidae, Heteropneustidae and Poeciliidae.
Among these, Cyprinidae was dominated in 41 per cent of monitored
lakes, followed by Cichlidae (28 per cent), Poeciliidae (15 per
cent), Clariidae (9 per cent), Channidae (3 per cent), Ambassidae (1
per cent) and Heteropneustidae (1 per cent).
Figure 9.3: The Percentage Occurrence of Fish Orders (a) and
Families (b) in Lakes of Bangalore.Cyprinus
carpio, Ctenopharyngodon idella, Gambusia
affinis, Oreochromis sp., Clariasgarie pinus and
Hypophthalmichthys molitrix are exotic fishes recorded in
the current study. Clarias gariepinus is a hardy species
and can tolerate both oxygenated as well as poorly oxygenated
waterbodies (Ogundiran et al., 2010).
Table 9.1: Ichthyofauna Diversity in Lakes of Bangalore,
Karnataka
Ichthyofauna Diversity in Relation to Water Quality of Lakes
of Bangalore
Sl.No. |
Fish Species |
Common Name |
Order |
Family |
Genus |
1 |
Catla catla |
Catla |
Cypriniformes |
Cyprinidae |
Catla |
2 |
Channa punctata |
Spotted Snakehead |
Perciformes |
Channidae |
Channa |
3 |
Channa striata |
Striped Snakehead |
Perciformes |
Channidae |
Channa |
4 |
Cirrhinus mrigala |
Mrigal |
Cypriniformes |
Cyprinidae |
Cirrhinus |
5 |
Clarias batrachus |
Walking catfish/Magur |
Siluriformes |
Clariidae |
Clarias |
6 |
Clarias gariepinus |
African catfish |
Siluriformes |
Clariidae |
Clarias |
7 |
Ctenopharyngodon idella |
Grass carp |
Cypriniformes |
Cyprinidae |
Ctenopharyngodon |
8 |
Cyprinus carpio |
Common carp |
Cypriniformes |
Cyprinidae |
Cyprinus |
9 |
Gambusia affinis |
Mosquitofish |
Cyprinodontiformes |
Poeciliidae |
Gambusia |
10 |
Heteropneustes fossilis |
Stinging catfish |
Siluriformes |
Heteropneustidae |
Heteropneustes |
11 |
Hypophthalmichthys molitrix |
Silver carp |
Cypriniformes |
Cyprinidae |
Hypophthalmichthys |
12 |
Labeo fimbriatus |
Fringed-lipped peninsula carp |
Cypriniformes |
Cyprinidae |
Labeo |
13 |
Labeo rohita |
Rohu |
Cypriniformes |
Cyprinidae |
Labeo |
14 |
Oreochromis mossambicus |
Mozambique tilapia |
Perciformes |
Cichlidae |
Oreochromis |
15 |
Oreochromis niloticus |
Nile tilapia |
Perciformes |
Cichlidae |
Oreochromis |
16 |
Parambassis ranga |
Indian glassy fish |
Perciformes |
Ambassidae |
Parambassis |
17 |
Poecilia reticulata |
Guppy |
Cyprinodontiformes |
Poeciliidae |
Poecilia |
18 |
Puntius ticto |
Ticto Barb |
Cypriniformes |
Cyprinidae |
Puntius |
Gambusia affinis and Poecilia reticulata feed
on larvae and is used for mosquito control (Mahapatra et
al., 2014). The invasion of exotic species results in
loss of native and endemic species (Singh et al., 2013;
Sandilyan, 2016). Exotic fish species were introduced in India
for aquaculture, aquarium, sport fishing, weed control,
etc. and the introduction of exotic species led to the
decline in native species of fish and biodiversity (Kumar,
2000).
Figure 9.4: Distribution of Catla and Oreochromis in
Bangalore Lakes.Among the 14 genera, Catla was
found in 32 lakes and Oreochromis was recorded in 29 lakes in the
current investigation (Figures 9.4 and 9.5). Based on the diet
(Table 9.2), fishes are grouped as herbivorous, omnivorous,
larvivorous, planktivorous and carnivorous. For example, Labeo
rohita (column and bottom feeder) prefers plant material
and decaying vegetation. Catla catla (surface feeder) feed
mainly on phytoplankton whereas Cirrhinus mrigala (bottom-feeder)
feed mainly on decaying vegetation (Chattopadhyay, 2017). Oreochromis
niloticus are opportunistic feeders and feed on detritus,
phytoplankton, crustacean, aquatic Ichthyofauna Diversity in Relation to Water Quality of Lakes
of Bangalore insects, small fish, zooplankton and macrophytes (Mohamed and
Al-Wan, 2020; Chatterjee et al., 2015).Under
conservation status as per IUCN (2010),one species was
categorized as critically endangered, one species under near
threatened, 13 under least concern and one species under
vulnerable category (Table 9.2).
Figure 9.5: Fish Genera found in Bangalore
LakesTable 9.2: List of Ichthyofauna,
their IUCN Status, Diet Pattern and their Benefits
Sl.No. |
Fish Species |
IUCN* |
Diet |
Benefits |
1 |
Catla catla |
LC |
Omnivorous |
Food fish |
2 |
Channa punctata |
LC |
Carnivorous |
Food fish |
3 |
Channa striata |
LC |
Carnivorous |
Food fish |
4 |
Cirrhinus mrigala |
LC |
Omnivorous |
Food fish |
5 |
Clarias batrachus |
LC |
Omnivorous |
Food fish |
6 |
Clarias gariepinus |
LC |
Omnivorous |
Food fish |
7 |
Ctenopharyngodon idella |
NE |
Herbivorous |
Control of weeds/
Food fish |
8 |
Cyprinus carpio |
CR |
Omnivorous |
Food fish |
9 |
Gambusia affinis |
LC |
Larvivorous |
Mosquito-control/ Ornamental |
10 |
Heteropneustes fossilis |
LC |
Omnivorous |
Food fish |
11 |
Hypophthalmichthys molitrix |
NT |
Planktivorous |
Food fish/controls
pest population |
Sl.No. |
Fish Species |
IUCN* |
Diet |
Benefits |
12 |
Labeo fimbriatus |
LC |
Herbivorous |
Food fish |
13 |
Labeo rohita |
LC |
Omnivore |
Food fish |
14 |
Oreochromis mossambicus |
VU |
Omnivorous |
Food fish |
15 |
Oreochromis niloticus |
LC |
Omnivorous |
Food fish |
16 |
Parambassis ranga |
LC |
Carnivorous/ Larvivorous |
Ornamental fish |
17 |
Poecilia reticulata |
NE |
Omnivorous |
Ornamental fish |
18 |
Puntius ticto |
LC |
Planktivorous |
Food fish/ Ornamental fish |
*LC: Least Concern; NE: Not Evaluated; CR: Critically Endangered;
NT: Near Threatened; VU: Vulnerable.
Indian major carps such as Catla catla, Cirrhinus
mrigala and Labeo rohita contribute 70 to 75 per
cent of the total freshwater fish production and have high
economic importance (Jayasankar, 2018). Genus such as Clarias,
Channa and Heteropneustes are air breathing fishes with good
market value for live fish (Thirumala et al., 2011).Dishes
prepared with fish flour (of Oreochromis niloticus) are
rich in proteins, lipids, essential amino acids, ash and
polyunsaturated fatty acids (PUFAs) (Alam and Aslam, 2020),
which highlights the need to conserve fish fauna to sustain food
and medicine to the dependent population.
Water Quality of Lakes
Health of aquatic ecosystems are assessed based on water quality
considering the physical, chemical and biological
characteristics of water. Evaluation of these parameters will
aid in understanding the suitability of lake water for biotic
consumption and health of a particular aquatic ecosystem. Fish
is very sensitive to variations in water quality and hence
considered as biological indicator in aquatic ecosystems. Thus,
it is necessary to understand the water quality of lakes or
habitat conditions of fishes. Physical, chemical and biological
parameters assessed in sampled lakes are discussed next.
Water Temperature and pH
Water temperature influences both the physico-chemical variables
and biological activities in the aquatic ecosystems. Temperature
affects the microbial (algae and bacteria) activities in water
as it influences the organic matter decomposition and nutrient
cycling. Temperature also affects the solubility of gases like O2,
CO2 and NH3 (Siriwardana et al., 2019).
Water temperature in the current study varied between 23.5oC to
34.2oC (Figure 9.6). pH varied among the monitored lakes and
found to range between 7.2 to 10.19, indicated an alkaline
nature of lake water (Figure 9.6). Ichthyofauna Diversity
in Relation to Water Quality of Lakes of Bangalore
Figure 9.6: The Variation of Water Temperature and pH across
Lakes of Bangalore.pH regulates many biological
processes and biochemical reactions. In case of pH, the desirable
range for fish culture is 6.5 - 9.0. Doddakallasandra had high
levels of pH among all the lakes due to high photosynthetic
activities by phytoplankton. The photosynthesis raises the pH
whereas respiration and decomposition processes lowers pH in lake
water. Fish have an average blood pH of 7.4, so the acceptable range
for fish culture would be 6.5 - 9.0. The pH in water ranging from
4.0 - 6.5 and 9.0 - 11.0 is stressful for fish growth and
reproduction. Fish death can occur at pH level of <4 or>11
(Ekubo and Abowei, 2011).
Total Dissolved Solids (TDS) and Electrical Conductivity
(EC)
Total dissolved solids in natural waters are mainly contributed
by the presence of carbonates, bicarbonates, sulphates,
chlorides, phosphates and nitrates of magnesium, calcium,
sodium, potassium, iron etc. and tiny amounts of
organic matter (Ramachandra et al., 2014). Electrical
conductivity gives the measure of the capacity of water to
conduct an electric current. When the concentration of dissolved
ions in water increases then, electrical conductivity also
increases. The value of total dissolved solids and electrical
conductivity in lakes ranged from 152.5 mg/L to 1548 mg/L and
306.67µS/cm to 2814 µS/cm, respectively (Figure 9.7). Lakes such
as Basapura-1 and Basapura-2 had higher ionic contents with
higher TDS and EC levels. The increased levels of dissolved and
suspended solids will decrease the dissolved oxygen levels in
aquatic ecosystems (Yýlmaz et al., 2020). The optimum
conductivity level for fish culture differs among different
species as they vary in their capability to maintain osmotic
pressure (Kumar et al., 2017).
Turbidity and Dissolved Oxygen (DO)
Turbidity occurs due to the presence of various suspended and
colloidal matter in lake water such as clay, silt, inorganic
matter, organic matter, plankton and tiny micro-organisms
(Ramachandra et al., 2018). Turbidity in monitored
lakes was found to range between10.14 NTU - 306.33 NTU (Figure
9.8) .High turbidity in lakes result in low light penetration to
bottom levels, reduces photosynthetic rate and may even cause
fish death due to clogging of gills (Saraswathy et
al., 2015). The concentration of dissolved oxygen in
lake water varies with temperature, amount of organic waste,
sediment quality/quantity, turbulence, photosynthetic rate and
respiration/decomposition (Devi et al., 2015). The
solubility of dissolved oxygen decreases under low atmospheric
pressure and high saline conditions (Rouse, 1979). The dissolved
oxygen levels ranged between 1.52 mg/L - 11.27 mg/L in lakes
with minimum value in Gangadharkere while maximum value in
Jakkur lake (Figure 9.8).
Biochemical Oxygen Demand (BOD) and Chemical Oxygen Demand
(COD)
Biochemical oxygen demand is the amount of oxygen utilized by
micro- organisms in stabilizing the organic matter (Davraz et
al., 2019). The chemical oxygen demand is the amount of
oxygen equivalent of the organic matter in lakeIchthyofauna
Diversity in Relation to Water Quality of Lakes of
Bangalore
Figure 9.7: Variation of Total Dissolved Solids and
Electrical Conductivity in Lakes of Bangalore.
Biodiversity Challenges: A Way Forward
Figure 9.8: The Turbidity and Dissolved Oxygen Levels in
Lakes of Bangalore.water that is susceptible to
oxidation with the help of a strong chemical oxidant. The BOD and
COD of lake water samples ranged between 7.45 mg/L - 99.59 mg/L and
11.33 mg/L - 150 mg/L, respectively (Figure 9.9). Both BOD and COD
of lake water increases with an increase in the organic matter
content due to organic pollution from point as well as non-point
sources.
Total Alkalinity and Chloride
Total alkalinity provides the measure of the ability of water to
neutralize acids. Alkalinity is due to the presence of
carbonates, bicarbonates and hydroxides of calcium, magnesium,
potassium, sodium and salts of borates, silicates, phosphates,
etc. (Sarkar et al., 2020, Qureshimatva et
al., 2015). The salts of sodium (NaCl), potassium (KCl)
and calcium (CaCl2) contribute chlorides in lake
water. The total alkalinity and chloride in sampled lakes were
recorded as 81.33 mg/L - 684.33mg/L and 25.56 mg/L - 1165.82
mg/L, respectively (Figure 9.10). The desired level of
alkalinity for fish culture is between 50-150 mg/L whereas the
desirable level of chlorides for catfish production is > 60
mg/L (Rajbongshi et al., 2016). The main source of
chloride in lake water include salt deposits, untreated sewage,
industrial effluents and through agricultural inputs (Sajeev
et al., 2020).
Total Hardness, Calcium and Magnesium
Total hardness is caused due to the presence of cations and
anions such as calcium and magnesium, carbonates, bicarbonates
and chloride in lake water (Kamboj and Kamboj, 2019). Calcium
levels in water help in osmoregulation under stressful
conditions and are important for egg and larvae development in
fishes. A calcium concentration of >400 mg/L is detrimental
to fish and crustaceans (Stone et al., 2013). Magnesium
generally occurs in lesser concentrations than calcium in lakes.
The total hardness ranged between 72 mg/L – 510 mg/L in sampled
lakes. Calcium and magnesium are necessary for metabolic
activities like bone and scale formation in fishes (Bhatnagar
and Devi, 2013). A hardness level of 150 mg/L is recommended for
the optimum growth and survival of Labeo rohita (Rajkumar
et al., 2018). The calcium and magnesium varied among
lakes and recorded as 14.43 mg/L - 160.32 mg/L and 3.72 mg/L -
42.41 mg/L, respectively (Figure 9.11).
Nitrate and Ortho-phosphate
Nitrate and phosphate are the limiting nutrients in aquatic
ecosystem. Nitrate ranged between 0.118 mg/L - 4.283 mg/L among
lakes of Bangalore (Figure 9.12).
The increased levels of nitrogen and phosphorus in water occurs
due to the discharge of untreated domestic wastes, industrial
effluents and agricultural runoff (Pinto et al., 2020).
In the present study, ortho-phosphate ranged between 0.06 mg/L -
4.41 mg/L (Figure 9.12). The increase of phosphorus levels in
freshwater are due to domestic, agricultural and industrial
inputs (external P loading) along with internal P loading from
the bottom sediments (Calijuri et al., 2002). The
extensive use of detergents and sewage are the major sources of
phosphates in lake
Biodiversity Challenges: A Way Forward
Figure 9.9: Concentration of BOD and COD in Lakes of
Bangalore.
Figure 9.10: Variation of Total Alkalinity and Chloride in
Lakes of Bangalore.
Biodiversity Challenges: A Way Forward
Figure 9.11: The Total Hardness and Calcium Levels in Lakes
of Bangalore.
Figure 9.12: Variation of Nitrate and Ortho-phosphate in
Lakes of Bangalore.water (Abdusalam et
al., 2019). Water rich in phosphorus favors the growth and
proliferation of algae, which results in the eutrophication in water
bodies (Rocha et al., 2015). Detergent effluents can induce
several toxicological effects in Clarias gariepinus (Ogundiran
et al., 2010; Nkpondion et al., 2016).
Factors Affecting Lake Water Quality
Principal component analysis (PCA) was applied to the normalized
data sets (i.e., 15 physico-chemical parameters of 36
lakes) to identify underlying factors affecting water quality of
lakes. The PC loadings of > 0.75, 0.75 - 0.50 and 0.50 - 0.30 were classified as ‘strong’, ‘moderate’ and ‘weak’
respectively (Liu et al., 2003). The principal
components (PCs) with eigenvalues greater than one (>1) were
considered significant to explain the whole dataset.
In the present study, four principal components were obtained
with eigenvalues greater than 1, that explained 81.4 per cent of
the total variance in the water quality dataset (Table 9.3). The
first component, PC1 accounted for about 47.5 per cent of the
total variance in the water quality data set. PC1 has positive
loadings on water temperature (0.50), TDS (0.94), EC (0.97),
total hardness (0.90), calcium (0.93), magnesium (0.53), chloride (0.88), turbidity (0.76), BOD
(0.83) and COD (0.76). This factor is attributed to ionic and
organic pollutants, which highlights of industrial and domestic
discharges.
Table 9.3: Loadings of Environmental Variables on
Principal Components for Water Quality Datasets
|
PC 1 |
PC 2 |
PC 3 |
PC 4 |
Water Temperature |
0.50 |
0.52 |
-0.02 |
-0.16 |
TDS |
0.94 |
-0.10 |
0.08 |
0.19 |
EC |
0.97 |
0.02 |
-0.04 |
0.15 |
pH |
0.15 |
0.57 |
0.61 |
0.07 |
Total Hardness |
0.90 |
-0.36 |
0.03 |
0.11 |
Calcium |
0.93 |
-0.17 |
-0.08 |
0.09 |
Magnesium |
0.53 |
-0.62 |
0.26 |
0.12 |
Chloride |
0.88 |
0.08 |
-0.16 |
0.25 |
Total Alkalinity |
0.41 |
-0.73 |
0.19 |
0.00 |
Turbidity |
0.76 |
0.40 |
-0.29 |
-0.15 |
DO |
0.06 |
0.51 |
0.18 |
0.73 |
BOD |
0.83 |
0.23 |
-0.08 |
-0.35 |
COD |
0.76 |
0.30 |
-0.33 |
-0.18 |
OP |
0.45 |
-0.34 |
0.53 |
-0.36 |
Nitrate |
0.28 |
0.58 |
0.53 |
-0.22 |
Eigenvalue |
7.1 |
2.7 |
1.3 |
1.1 |
Per cent variance |
47.5 |
18.0 |
8.7 |
7.2 |
PC2 accounted for about 18.0 per cent of the total variance with
positive loadings of water temperature (0.52), pH (0.57),
nitrate (0.58) and DO (0.51) and negative loadings of magnesium
(-0.62) and alkalinity (-0.73). This factor corresponds to
organic pollution and relates to the productivity of freshwater
ecosystem. The PC3 explained 8.7 per cent of the total variance
with positive loadings of ortho- phosphate (0.53), nitrate
(0.53) and pH (0.61). This factor represents the varied sources
of nutrient pollution due to domestic sources, agricultural
activities (fertilizer input), industrial discharges and
urbanization (urban wastewater). PC4 explained 7.2 per cent of
the total variance and is related to DO (0.73) which suggests
that lakes had enough amount of dissolved oxygen to sustain
aquatic life. A healthy aquatic ecosystem holds DO level of 4 -
6 mg/L (Avvannavar and Shrihari, 2008). DO varies with time,
season, rate of photosynthesis, decomposition and respiration
activities in lake water. The untreated sewage flowing into
lakes alters water chemistry by increasing the ionic, organic
and nutrient contents.
WQI Status of Lakes in Bangalore
WQI is computed considering ten water quality parameters - pH,
electrical conductivity, total dissolved solids, dissolved
oxygen, total hardness, calcium, magnesium, chloride, total
alkalinity and nitrate. The water quality condition is described
on the basis of WQI value in the range of 0-25, 26-50, 51-75,
76-100 and >100 which corresponds to excellent, good, poor,
very poor and unsuitable respectively. Overall, Water quality
index (WQI) for the lake water samples were found in the range
of 38 to 122 (Figure 9.13).
In the current study on lakes of Bangalore, about 5 per cent of
lakes (Lalbagh and Yediyur) fell under good category while 31
per cent lakes fell under poor category. Majority of lakes
(about 56 per cent) were classified under very poor category.
Lakes namely Basavanapura, Mallathahalli and Sheelavanthakere
which fell under the category of unsuitable (8 per cent), is not
appropriate for fish culture. The water quality of lakes is
deteriorating as evident from WQI status of lakes, mainly due to
the inflow of sewage water from residential and commercial
complexes, agricultural run-off, anthropogenic activities,
untreated effluents from industries and factories, dumping of
solid wastes into lakes and lack of proper sanitation.
In earlier studies, WQI values of Sankey tank water belonged to
good water class whereas Mallathahallilake fell under poor water
category (Ravikumar et al., 2013). WQI values of
Hebballake fell under very poor category (Sudarshan et
al., 2019). Earlier study has reported WQI of 3 lakes
in Haryana of > 100, indicating that water is unsuitable for
drinking, outdoor bathing and other uses (Kumar et
al., 2018). WQI status of Pariyejlake is poor and unfit
for human consumption (Thakor et al., 2011).
Anthropogenic stress caused the deterioration of water quality
of Dal lake as evident from WQI i.e., polluted and
unfit for human consumption (Ahmad et al., 2020).
Figure 9.13: WQI Status of Lakes of Bangalore.
Water quality parameters such as temperature, suspended solids,
pH, DO, ammonia, nitrite, carbon-dioxide and alkalinity play a
crucial role in the growth, reproduction and survival of fish
(Okoliegbe et al., 2020). The diversity and
distribution of ichthyofaunais governed by pH, turbidity and
electrical conductivity (Shetty et al., 2015). The
climate change with a decline in rainfall and delayed monsoon,
affects temperature of freshwater ecosystems and the breeding
behavior/ ecology of fishes (Ninawe et al., 2018). The
growth rate of Oreochromis niloticus increased at
higher temperature and DO whereas the growth rate declined under
increased pH, conductivity and ammonia levels (Makori et
al., 2017). The sewage and industrial effluents let
into water bodies increases the levels of total suspended
solids, total dissolved solids, COD and BOD (Ramanujam et
al., 2014). The detergent effluents in lake water
induce severe damage to gills, skin, kidney, heart, liver and
brain of fish (Nkpondion et al., 2016).Inorganic
pollution from industries is another main threat to ichthyofauna
(Rao et al., 2014). The waterdepth, pressure,
turbulence, temperature, light and turbidity are important for fish culture
(Priyamvada et al., 2013), which necessitates maintaining water quality to sustain
fish production.
In 1970s, about 55 fish species were recorded in Bangalore. At
present, there is a massive reduction in ichthyofauna diversity
in Bangalore as the lakes are under threat due to water
pollution,urbanization, encroachment of lakes, habitat loss or
habitat degradation, invasion of exotic species, agricultural
practices, climate change,flood, drought, over-harvesting of
fish resources and loss of interconnectivity among lakes. The
anthropogenic activities, water pollution, eutrophication,
habitat degradation, overexploitation, hydrologic alterations,
flow modification, damconstruction and climate change are the
major threats to fish biodiversity (Borah and Das, 2020; Bhakta
et al., 2019; Gupta et al., 2015; Vijaylaxmi
et al., 2010). Introduction of exotic species and
adopting destructive fishing method such as dynamite or
poisoning would cause serious threat to native ichthyofauna
(Bose et al., 2019). Urbanization, pollution and water
abstraction for irrigation and power generation impose threat to
fish diversity (Kumar Sarkar et al., 2013). Hence, it
is essential to regulate the sustained inflow of untreated
sewage and industrial effluents into lakes to maintain the
integrity of aquatic ecosystems and sustain fish diversity. The
nutrient removal in lakes (bioremediation) can be achieved in a
cost effective way through the integration of conventional water
treatment methods with the constructed wetlands (macrophytes)
and algal pond (Ramachandra et al., 2018).In order to
increase the ichthyofauna diversity, there is a need to avoid
habitat destruction, control pollution sources, should ban the
introduction of invasive species, harvesting of fish during the
spawning period and the harvesting of juveniles. Environmental
awareness through awareness programs would help in educating
public on the impacts of water pollution on freshwater fish and
also the role of healthy ecosystem in supporting people’s
livelihood. Regular workshops and awareness programs on wetland
goods and services would also help in the conservation of
aquatic biodiversity.
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