Biological Analysis of Small Reservoir Budha Talab in Raipur
Raghav M. and Biswas
P.
Department
of Fisheries, I.G.K.V, Raipur, India
ABSTRACT
Budha Talab
is the largest pond (30.25 ha.) among total 22 ponds present in the Raipur
city. It receives domestic waste and sewage and also used for cloth washing,
animal bathing and therefore water quality is fast deteriorating. Total 24
phytoplankton and 10 zooplankton species were identified. Among phytoplankton Scenedesmus sp., Microcystis
sp., Oscillatoria sp., Anabaena sp.,
Melosira sp., Nitzchia
sp., Chlorella sp. and among zooplankton Daphnia sp., Moina sp., Diaphanosoma
sp. were found throughout the year. Microcystis
sp., Oscillatoria sp., Melosira sp., Anabaena sp.
(phytoplankton) and Brachionus sp. and
Keratella sp. (zooplankton) indicate organic
pollution and eutrophic nature of Budha
Talab.
INTRODUCTION:
Reservoirs
which are situated near human settlements are greatly influenced with the
habitation viz. with disposal of sewage, soap and detergents and
industrial wastes. In developing countries like India where only few of the big
cities posses sewage treatment plants, the proper
disposal of sewage is an acute problem. Most of the city sewage and domestic
water is disposed into rivers, reservoirs and ponds without any treatment.The sewage water is rich in phosphate due to
extensive use of hard and /or soft detergents. It is estimated that about 800 x
106 gallons/day of sewage and sullage can
yield an annual out turn of 60,000 t N P K. Domestic sewage contains 250-400 ppm Organic Carbon and 80-120 ppm
total nitrogen with a C: N ratio of 3:1
(Mukhophodhyay and Sarangi,
2006). Even small addition of organic matter eutrophicates
reservoirs and stimulates bloom in the chain of waters connected to them (Sreenivasan, 1969). Raipur is known as city of ponds. Once
upon a time there were 70 ponds (1977) in Raipur city (Marothia,
1997) while reduced to 40 in 1997, but as of today there exists only 22 ponds. Vivekanada sarovar (popularly
known as Budha Talab) is
the largest tank in the city of Raipur (21014’N, 81038’E).
It is surrounded by thick dense habitation. Therefore, Physico-chemical
and biological conditions of water get affected due to human interference.
Surface water samples
were collected at monthly intervals for twelve months (July 2005-June 2006)
from three sampling sites between 2 p.m. to 5 p.m. from Budha
Talab. There were three
sampling sites-
Site-1 Near outlet (Southern side).
Site-2 Near Vivekananda statue
Site-3 Near Shyam takies (Northern side)
Plankton
was collected from surface water by plankton net and sample was fixed in 5%
formaldehyde and Lugol’s solution for zooplankton and
phytoplankton respectively.
The plankton samples
were stored in plastic bottles and observed under compound microscope for
identification. The plankton and algae were identified with the help of various
keys e.g. Needham (1962), Cramar (1984), Plaskitt (1997), Sinha and Naik (1997) and APHA (1998). Quantitative analysis of
plankton was done by Sedgwick Rafter cell. Primary productivity was measured by
light and dark bottle method (APHA, 1998). Light and dark DO bottles (300ml)
were placed at one-foot depth and kept incubated for 3 hours. After 3 hours
bottles were taken up and oxygen was fixed with Winkler’s A and Winkler’s B
solution. The result is expressed in mg C/cm 3/h.
RESULT AND
DISCUSSION:
The monthly distributions of phytoplankton
are given in Table-4.2. Twenty
four phytoplankton species were identified and among them 13 were represented
by Chlorophyceae, 5 species of Cyanophyceae,
4 of Bacillariophyceae and 2 species of Euglenophyceae. Among phytoplankton Chlorophyceae
was also found to be a dominant group (Selot, 1977).
Six genera observed by Palmer (1969) are common with present study (Euglena
sp., Oscillatoria sp., Scenedesmus
sp., Chlorella sp., Nitzchia sp.
and Navicula sp.). Among Chlorophyceae
Actinastrum sp., chlorella sp.,
Scenedesmus sp., Richtirella
sp.; among Cyanophyceae, Microcystis
sp., Anabaena sp., Oscillatoria sp.
were found throughout the year in all months. Among Bacillariophyceae Melosira
sp. and Nitzchia sp. and
among Euglenophyceae Euglena sp. was found in
all months over the year. The presence of Microcystis
sp. indicates the eutrophic nature and the organic
pollution in the pond as indicated by Ganapati (1940)
and Singh (1955). The presence of other species like Oscillatoria,
Scenedesmus, Chlorella and Nitzchia
indicate organic pollution as also reported by Rao et
al. 1978) and Mukhopadhaya and Sarangi (2006). Kanungo, 1987)
identified Melosia sp as bioindicator of pollution and this species was found almost
throughout the year. Most of these phytoplankton found in our study indicated
that, the pond is organically polluted with eutrophic
condition. It is also proved by palmer
Index (1969) that six phytoplankton genera found in Budha
Talab stand in first seven genera listed given by
Palmer.
Zooplankton
Monthly variation in zooplankton population
is given in Table- 4.1. Quantitative values of zooplankton show significant
variation over the months. The highest number was recorded in the month of July
(252 no./l) and the lowest was in the month of March
(93 no./l). In this study it was seen that, phytoplankton were predominant over
zooplankton. Sarwar and Parveen
(1996) opined that, higher zooplankton was recorded in summer but in present
study higher zooplankton were observed in late summer or monsoon. Sukumaran and Das (2002) also found higher zooplankton in
monsoon (July).
Zooplankton population in the water of the Budha Talab mainly consisted of
four major groups: Protozoa, Rotifera, Cladocera and Copepoda. Total 10
species of zooplankton were identified, among which 1 was represented by Protozoa,
2 by Rotifera, 4 by Cladocera
and 3 by Copepoda. Protozoans
were represented by Zoothamnium sp., Rotifera by Brachionus sp.
and Keratella sp., Cladocera
by Daphnia sp., Moina sp., Bosmina sp. and Diaphanosmona
sp.. Among Copepod, Diaptomus
sp. and Cyclops sp. were found in all most all the months. Vasisht and Sra (1979) while studying the Chandigarh
wastewaters recorded, characteristics of many species
of Zooplankton as bio indicator of population. Keratella
sp. was observed to be present in both the studies. Sampath
et al. (1979) in their studies on water quality of river Cauvery
concluded that, Brachionus sp. might be
used as bio indicator of pollution. Arora (1963) and
Khan (1967) have also observed that Brachionus
sp. was abundant in moderately polluted water. This could mean that the
presence of Brachionus sp. and Keratella sp. indicate polluted state with eutrophic nature of Budha Talab.
Productivity
studies
Gross primary productivity (GPP)
In this study the highest GPP recorded was
850 (mgC/m3/h) in the September and the
lowest was 375 (mgC/m3 /h) in the June
(Tab 4.1). Seasonal mean GPP were respectively 729.3 (mgC/m3/h)
in monsoon and 475 (mgC/m3/h) in spring.
GPP varied significantly over the months and seasons. A significant
relationship between GPP and phytoplankton is relatively a good index of
productivity. Similar results were also obtained by Basheer
(1996.).
Net primary productivity (NPP)
The highest net primary productivity recorded
in September was 197 (mgC/m3 /h) and the
lowest in February was 114(mgC/m3 /h).The
NPP varied significantly over the months. The water temperature and
transparency played an important role in determining pond productivity (Ali and
Khan, 1978 and Ayyappan and Gupta, 1985). however, no such relationship was found in this study.
Fig. A
Fig. B
Fig. C
Fig-1: Monthly variation in phytoplankton (Fig. A), zooplankton
(Fig. B) and GPP and NPP (Fig. C)
|
Zooplankton |
July |
Aug |
Sep |
Oct |
Nov |
Dec |
Jan |
Feb |
March |
April |
May |
June |
Protozoa
|
||||||||||||
|
Zoothanium sp |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
- |
- |
- |
- |
+ |
Rotifera
|
||||||||||||
|
Brachionus sp |
+ |
+ |
- |
+ |
- |
+ |
+ |
- |
+ |
- |
- |
- |
|
Keratella sp |
+ |
+ |
+ |
+ |
- |
+ |
+ |
- |
+ |
- |
+ |
+ |
Cladoceara
|
||||||||||||
|
Moina sp |
+ |
+ |
+ |
- |
+ |
- |
+ |
- |
- |
- |
- |
+ |
|
Daphnia
sp |
+ |
+ |
+ |
- |
- |
- |
- |
+ |
- |
+ |
+ |
- |
|
Bosmina sp |
+ |
+ |
+ |
- |
+ |
+ |
- |
- |
- |
- |
- |
+ |
|
Diaphanosmona sp |
+ |
+ |
+ |
- |
- |
|
- |
+ |
- |
+ |
- |
- |
Copepoda
|
||||||||||||
|
Diaptomus sp |
+ |
+ |
+ |
+ |
+ |
- |
+ |
+ |
+ |
+ |
+ |
+ |
|
Cyclops
sp |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
|
Rhinediaptomus sp |
+ |
- |
+ |
+ |
- |
- |
- |
- |
- |
+ |
+ |
- |
Total
zooplankton (no./L)
|
252 |
216 |
155 |
125 |
122 |
134 |
107 |
123 |
94 |
116 |
144 |
174 |
|
SEm |
±9.54 |
|||||||||||
|
CV (%) |
11.26 |
|||||||||||
|
Family/Genera |
July |
Aug |
Sep |
Oct |
Nov |
Dec |
Jan |
Feb |
March |
April |
May |
June |
|
|
Chlorophyceae |
|||||||||||||
|
Actinastrum sp |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
|
|
Ankistrodesmus sp |
+ |
- |
- |
- |
+ |
+ |
- |
- |
- |
- |
- |
- |
|
|
Botryococcus sp |
- |
- |
- |
- |
- |
- |
+ |
+ |
+ |
+ |
- |
+ |
|
|
Crucigenia sp |
+ |
+ |
+ |
+ |
- |
- |
- |
- |
- |
+ |
+ |
+ |
|
|
Chlorella sp |
- |
- |
+ |
- |
- |
- |
- |
+ |
- |
+ |
- |
- |
|
|
Clostrum sp |
- |
+ |
+ |
+ |
- |
- |
+ |
- |
- |
- |
+ |
+ |
|
|
Scenedesmus sp |
+ |
+ |
+ |
+ |
+ |
- |
+ |
+ |
+ |
+ |
+ |
+ |
|
|
Cladophora sp |
+ |
+ |
+ |
- |
-+ |
- |
- |
+ |
- |
+ |
+ |
- |
|
|
Anacystis sp |
+ |
+ |
+ |
- |
+ |
- |
- |
- |
- |
+ |
+ |
- |
|
|
Volvox sp |
- |
- |
+ |
- |
- |
+ |
- |
- |
- |
+ |
- |
+ |
|
|
Tetraspora sp |
+ |
- |
+ |
- |
- |
- |
- |
- |
- |
- |
+ |
- |
|
|
Selenostrum sp |
- |
- |
- |
+ |
+ |
+ |
+ |
- |
+ |
- |
+ |
- |
|
|
Richtrella sp |
+ |
+ |
+ |
+ |
+ |
- |
+ |
- |
+ |
+ |
- |
- |
|
|
Cyanophyceae |
|||||||||||||
|
Mycrocystis sp |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
|
|
Oscillatoria sp |
+ |
+ |
+ |
+ |
+ |
- |
|
+ |
+ |
+ |
- |
+ |
|
|
Spirulena sp |
+ |
+ |
- |
- |
+ |
- |
+ |
- |
+ |
-- |
+ |
+ |
|
|
Anabaena sp |
+ |
+ |
+ |
+ |
+ |
- |
-- |
+ |
+ |
+ |
+ |
+ |
|
|
Synechocystis sp |
+ |
+ |
+ |
+ |
- |
- |
- |
+ |
- |
- |
+ |
+ |
|
|
Bacillariophycae |
|||||||||||||
|
Melosira sp |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
- |
- |
+ |
+ |
|
|
Navicula sp |
+ |
+ |
- |
- |
- |
- |
- |
- |
- |
-- |
+ |
+ |
|
|
Nitzchia sp |
+ |
+ |
+ |
+ |
+ |
- |
+ |
+ |
+ |
+ |
+ |
+ |
|
|
Stephnodiscus sp |
+ |
+ |
+ |
+ |
+ |
- |
- |
+ |
|
+ |
+ |
+ |
|
|
Euglenophyceae |
|||||||||||||
Phacus sp
|
+ |
+ |
- |
- |
- |
- |
- |
-- |
- |
- |
+ |
+ |
|
Euglina sp
|
+ |
+ |
- |
- |
- |
- |
+ |
- |
- |
- |
- |
+ |
|
Total phytoplankton (no./L)
|
905 |
1167 |
1606 |
1496 |
1343 |
819 |
720 |
542 |
777 |
842 |
894 |
914 |
|
SEm
|
±36.10 |
||||||||||||
|
CV (%) |
6.24 |
||||||||||||
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Received on 20.11.2009
Accepted on 27.12.2009
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