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IJEDR

International Journal of Ecology and Development Research


Vol. 4(1), pp. 044-052, March, 2018. © www.premierpublishers.org. ISSN: 2326-7204

Research Article

The Contribution of Phytoplankton to the Primary Production


in Floodplain Lakes (Chaurs) of North Bihar, India
1AK Singh, 2*Rani Kumari, 3Arun Kumar
1,2
Department of Zoology, B.D. College (Magadh University), Patna 800 001, India
3
P.G. Department of Zoology, B.N. Mandal University, Madhepura 852 113, India

This study aimed to estimate photosynthetic productivity of phytoplankton and water quality in
two floodplain lakes of north Bihar, India. Gross phytoplankton productivity ranged from 1.849 g
Cm-2day-1 to 4.994 g Cm-2day-1 at Tarawe chaur and 1.319 g Cm-2day-1 to 3.965 g Cm-2day-1 at
Gamharia chaur. The net primary productivity measured as 1.037 g Cm-2day-1 to 3.849 g Cm-2day-1
at Tarawe chaur and 1.003 g Cm-2day-1 to 2.621 g Cm-2day-1 at Gamharia chaur. Primary productivity
(GPP and NPP) of phytoplankton show a single annual peak. Respiration rates varied between
0.428 g Cm-2day-1 to 2.017 g Cm-2day-1 at Tarawe chaur and 0.489 g Cm-2day-1 to 1.475 g Cm-2day-1 at
Gamharia chaur. Seasonal variation in phytoplankton gross and the net productivity was almost
similar, highest in summer and lowest in winter. NPP/GPP ratio and respiration as percentage of
gross production were computed. Physico-chemical parameters of water were analysed
concurrently.

Keywords: Floodplain lakes, phytoplankton productivity, water quality, environmental factors, correlation

INTRODUCTION

Wetlands situated on flood plains of major river systems chemosynthetic bacteria etc.) may occur, but usually
are one of the most highly productive ecosystems on earth. contribute less to primary production (Robertson et al.,
Floodplain wetlands are frequently found at the interface 2001). More recently, the impact of solar radiation on the
between terrestrial and aquatic ecosystems. Besides aquatic ecosystem and primary production has been
supporting a wide range of biological diversity and discussed and measured in temperate and tropical regions
important fisheries they offer spawning and nursery areas of the world (Rogers and Ralph, 2010). In India, a large
for many riverine fish. Biotic interactions and the number of studies have been made on the physical,
productivity of these wetlands are strongly influenced by chemical and biological characteristics of floodplain
the flood condition (Junk et al., 1989). Despite of the wetlands, but, estimation of primary productivity is ignored.
ecological importance, little information is available on However, in recent year, primary productivity of
productivity of floodplain wetlands. photosynthetic communities in wetlands have highlighted
by some workers (Sugunan et al., 2000; Datta, 2003; Palui
Primary productivity is the rate at which solar energy is and Jha, 2003; Baruah, 2003; Sarma et al., 2007; Banerjee
converted to organic compounds by the autotrophs or and Chattopadhyaya, 2008; Sharma, 2010; Dash et al.,
primary producers that is available to next trophic level 2011; Ziauddin et al., 2013), but, information from north
(Odum, 1971; Wetzel and Likens, 1979), thus forms base Bihar is lacking.
of food chain (Helbling and Villafane, 2009). Measuring
primary productivity of aquatic ecosystem is crucial for
understanding the trophic status in relation to maximizing *Corresponding author: Rani Kumari, Department of
fish production (Oglesby, 1977; McConnell et al., 1988). Zoology, B.D. College (Magadh University), Patna 800
Phytoplankton, periphyton and macrophytes are the most 001, India. E-mail: ranikumari2474@gmail.com Tel:
important primary producers in lakes ecosystems. Other +919470667254, +919431950370 Co-Authors:
primary producers (e.g. photosynthetic and 1arnksingh@gmail.com, 3prf.arunkumar@gmail.com

The Contribution of Phytoplankton to the Primary Production in Floodplain Lakes (Chaurs) of North Bihar, India
Singh et al. 045

North Bihar is endowed with a large number of floodplain the light and dark bottles relative to the initial oxygen, the
wetlands, called mans (ox-bow lakes), chaurs (tectonic rate of primary production can be calculated (Jhingran et
depressions/floodplain lakes) and dhars (old-channels), al., 1969) and expressed as g C m-2d-1. Oxygen values
covers area of 40,000 ha (Sugunan and Bhattacharjya, were converted to carbon values by multiplying with the
2000). Among the wetlands, floodplain lakes are critical, factor 0.375 (Sreenivasan, 1964). The physico-chemical
they are the sources of food, income and with a huge parameters were analysed following standard methods
fishery potential with more fish species. Keeping in view (APHA, 1989; Trivedy and Goel, 1986). Pearson’s
the need for maximizing fish production, the present study correlation analyses were made to assess relationships
was carried out to estimate the primary production of between primary productivity and water parameters.
phytoplankton and to provide information on water quality
in floodplain lakes of north Bihar, India.
RESULTS AND DISCUSSION

MATERIALS AND METHODS Physico-chemical characteristics of water

Study area Changes in water quality regulate the rates of primary


productivity by limiting characteristics of the autotrophs or
The study was conducted in floodplain lakes, namely primary producers. Table 1 summarizes the water quality
Gamharia chaur and Tarawe chaur located in Madhepura of floodplain lakes.
district of Bihar, India. Both lakes are situated in the river
Kosi basin at 26o8′N latitude and 86o5′E longitude 23 km The selected lakes were shallow water bodies, therefore
north of Madhepura town. Location of the floodplain lakes heated up rapidly by the sun’s radiation, increase in
is shown in Figure 1. The selected lakes are located in temperature increasing chemical and biochemical
similar geographical area and climate, but, vary in shape, reaction, which ultimately affects primary productivity
size and depths. Seasonal flooding and rainwater runoff agrees with the findings of previous workers (Sugunan et
are major source of water. Of the two lakes, Gamharia al., 2000). Light is a central factor limiting natural
chaur is small shallow lake lies close to Gamharia village, productivity, Secchi dish visibility was high at Tarawe
covers an area of 10 ha with mean depth of 1.5 m and chaur (34.82±17.10 cm), though, the discharge of waste
receive domestic waste water continuously from village. water reduces water clarity at Gamharia chaur
This lake is located near NH-106, usually infested by water (27.92±11.56 cm), which in turn affecting productivity.
hyacinth (Eicchornia sp). Tarawe chaur is a large lake Conductivity was high at Gamharia chaur (284.04±108.24
located 3 km north from Gamharia chaur. The size of lake µmho cm-1) could be due to release of waste water from
is 21 ha with mean depth of 2.3 m. Marginal area is village increase ionic concentrations. pH falls within acidic
occupied by floating macrophytes. These lakes serve as to alkaline range. The removal of free carbon dioxide
fishing ground, a place for fish production and aqua-fruits during photosynthesis increases pH at Tarawe chaur (6.9-
cultivation. Water is used for agriculture and irrigation. 8.3), while the respiratory release of carbon dioxide might
be the reason for lower pH at Gamharia chaur (6.2-7.9).
Water sampling and analyses DO was higher at Tarawe chaur (5.2 mgl-1 to 8.9 mgl-1)
might be due to more light penetration in water, thus
Monthly productivity experiments were conducted in situ facilitating high rate of photosynthesis. The lower DO at
from November 2012 to October 2013. Rates of Gamharia chaur (4.9 mgl-1to 7.4 mgl-1) could be due to the
phytoplankton primary production and respiration were microbial breakdown of organic wastes consuming oxygen
measured using the light-dark bottle incubation method agrees with the findings of some workers (Moundiotiya et
(Gaarder and Gran, 1927). Light bottle allows al., 2004). Carbon dioxide is used in photosynthesis hence
photosynthesis and respiration, and dark bottles permit it is vital for primary productivity. Free carbon dioxide was
only respiration. Winkler’s method was followed for oxygen recorded only in monsoon might be due to high
determination (APHA, 1989). For the analysis of primary decomposition rates of waste materials release carbon
productivity water samples were taken from lakes with a dioxide (Sugunan et al., 2000), though, its concentration
one-liter polyethylene bottle from the selected depth (30 was very low agreeing with the findings of some workers
cm below the surface water). The samples collected (Sugunan et al., 2000). Carbonate and bicarbonate are the
contain planktonic organisms including phytoplankton. The major source of alkalinity. Carbonate was observed when
light and dark bottles filled in duplicate with same water. the carbon dioxide was absent. Bicarbonate was higher at
Oxygen of one light bottle was measured immediately Gamharia chaur (176.26±32.30 mgl-1) probably due to the
regarded as the initial level of oxygen. The remaining disposal of nutrient-rich wastes from village. Calcium and
bottles were placed in situ at the same depth and place. magnesium concentration was too low reflecting soft-water
Incubation was done for 6 hrs (9.00 am to 3.00 pm). The characteristics might be due to high rate of cations (Ca +2
bottles were removed at the end of the experiments and and Mg+2) assimilation by the aquatic plants. Chloride
analysed for oxygen. From the difference in oxygen within concentration was not alarming, however, its higher value
The Contribution of Phytoplankton to the Primary Production in Floodplain Lakes (Chaurs) of North Bihar, India
Int. J. Ecol. Devel. Res. 046

at Gamharia chaur probably due to addition of waste water productivity ranged from 2.7 g C m -2d-1 to 4.27 g C m-2d-1
from human habitation and cattle-shed. Nitrogen and and net productivity 2.05 g C m -2d-1 to 2.80 g C m-2d-1 in
phosphorus are regarded as primary productivity limiting beels of Assam (Sarma et al., 2007). Highest gross and
nutrients. In this study, nitrate-N and phosphate-P falls net primary productivity in beels of Assam was 0.847 mg
within productive range. The lakes receive nitrogen and C m-3h-1 and 0.798 mg C m-3h-1 (Hazarika, 2010). Gross
phosphorus either naturally from flooding or through runoff primary productivity of phytoplankton ranged from 2.88 g
from nutrient-rich agricultural fields agrees with the C m-2d-1 to 4.66 g C m-2d-1 and the net productivity 1.72 g
findings of some workers (Ganesan and Khan, 2008; C m-2d-1 to 2.94 g C m-2 d-1 in riverine wetlands of Assam
Sharma, 2010). Low BOD at Tarawe chaur (1.4 mgl-1 to (Sarma et al., 2013). The primary production rates as
2.9 mgl-1) show a good water quality while the high at obtained in the present study are comparatively high as
Gamharia chaur (2.1 mgl-1 to 6.1 mgl-1) reveal decline in reported from other wetland this indicates that a large
water quality might be due to release of organic waste- amount of organic production is available to next trophic
loaded water from village (Moundiotiya et al., 2004). level. High primary production at Tarawe chaur showed a
Overall water quality was similar in the lakes as they good trophic condition maybe due to better conversion rate
receive water from same sources. of solar energy into chemical energy.

Primary productivity Seasonal variation in phytoplankton primary productivity


show an increasing trend from winter, reached highest in
Gross and net primary productivity, respiration, NPP/GPP summer and then decline in monsoon. Gross and net
ratio and respiration as percentage of gross data are primary productivity in this study showed a single annual
summarized in Table 2. Seasonal variation is shown in peak, although, some workers reported bimodality in
Figure 2 to 4. Correlation analysis data is given in Table 3. riverine wetlands (Sarma et al., 2007). Phytoplankton
In this study, gross primary production of phytoplankton primary productivity was high in summer might be due to
ranged from 1.849 g C m-2d-1 to 4.994 g C m-2d-1 at Tarawe greater light intensity, long photoperiods and high
chaur and 1.319 g C m-2d-1 to 3.965 g C m -2d-1 at Gamharia temperature increase photosynthetic production agree the
chaur. Mean phytoplankton GPP was 2.872±1.11 g C m- findings of some workers (Sugunan and Bhattacharjya,
2d-1and 2.395±0.78 g C m-2d-1 (Table 2). Net primary 2000), while, the low during winter could be due to low
productivity (NPP) is the GPP minus the organic matter temperature, poor light intensity and short photoperiods. In
consumed as energy source in the metabolisms of spite of these, there are numerous factors that determine
producers. Net phytoplankton production was less than of photosynthetic rate of phytoplankton. GPP showed
gross production ranged from 1.037 g C m-2d-1 to 3.849 g significant (p>0.01) positive correlation with water
C m-2d-1 at Tarawe chaur and 1.003 g C m-2d-1 to 2.621 g temperature (r=0.674), chloride (r=0.619) and magnesium
C m-2d-1 at Gamharia chaur. Mean NPP was 1.854±0.84 g (r=0.752) and significant negative correlation with
C m-2d-1and 1.385±0.54 g C m-2d-1 (Table 2). The two lakes carbonate (r=-0.630) at Tarawe chaur, while, it depicted
did not differ much in overall rate of gross and net primary significant positive correlation with water temperature
production. When the obtained value of primary (r=0.543), magnesium (r=0.566) and calcium (r=0.559) at
productivity compared with range reported from others Gamharia chaur (Table 3). The net primary productivity
wetlands showed that it varies tremendously in terms of can be influenced by the different light environments and
gross and net primary productivity. Primary productivity of increase in rates of respiration (Hubas et al., 2006). Net
an ox-bow lake of Kashmir was 2112 mg C m-2d-1 (Vass productivity provides the energetic and material basis for
and Langer, 1990). Net primary productivity was 41.8 mg all heterotrophic life. The NPP showed significant (p>0.01)
C m-3h-1 in floodplain lakes of West Bengal (Vinci and positive correlation with water temperature (r=0.516),
Mitra, 2000). Net phytoplankton production varied from calcium (r=0.655), magnesium (r=0.797) and chloride
110 mg C m-2d-1to 1750 mg C m-2d-1in beels of Assam (r=0.682) and significant negative correlation with
(Sugunan and Bhattacharjya, 2000). Mean gross and net carbonate (r=-0.638) at Tarawe chaur, but, it showed
primary production was 1148.13±246.80 mg C m-3d-1 and significant positive correlation with calcium (r=0.552) and
548.41 ± 86.78 mg C m-3d-1 in ox-bow beels of magnesium (r=0.540) at Gamharia chaur (Table 3).
Brahmaputra floodplain (Baruah, 2003). Phytoplankton
productivity ranged from 2220 mg C m-2d-1 to 2919 mg C During the periods of flooding, phytoplankton density
m-2d-1 in floodplain wetlands of Bihar (Palui and Jha, 2003). declined abruptly, which in turn affects lake productivity
Net primary productivity varied between 12.5 mg C m-3h-1 agrees with findings of some workers (Sarma et al., 2007).
to 412.5 mg C m-3h-1 in wetlands of West Bengal (Datta, Furthermore, when the floodwater recedes, density of
2003). Net productivity fluctuates between 150 mg C m-3h- phytoplankton increase sharply dominates ecosystem,
1 to 137 mg C m -3h-1 in Loktak Lake of Manipur (Mukherjee latter on aquatic macrophytes become dominant
et al., 2006). Gross productivity of phytoplankton ranged communities. The rates of primary productivity increased
from 0.389 g C m-2d-1 to 1.393 g C m -2d-1 and the net with increasing temperature (Davison, 1991). The results
productivity 0.294 g C m -2d-1 to 9.699 g C m-2d-1 in beels of contradict this pattern as phytoplankton production was
West Bengal (Chaudhuri, 2007).Gross phytoplankton low in monsoon when the temperature was high. This
The Contribution of Phytoplankton to the Primary Production in Floodplain Lakes (Chaurs) of North Bihar, India
Singh et al. 047

means, temperature is not solely responsible for limiting differences in ecological condition, size and depth.
primary productivity agrees with the findings of some NPP/GPP ratio was low in monsoon might be due to the
workers (Banerjee and Chattopadhyaya, 2008; Dash et al., rainfall and floodwater dilutes phytoplankton density
2011). Gross and net production was highest at Tarawe (Singh and Singh, 1999). The NPP/GPP ratio reflects
chaur might be due to the greater phytoplankton density, productivity potential of water body because it remains low
though, the lowest at Gamharia chaur could be attributed in productive ecosystem (Ganf and Horne, 1975).
to discharge of waste water interrupt functioning of aquatic NPP/GPP ratio less than 0.5 reveal eutrophication
ecosystem. Furthermore, invasion of floating macrophytes (Bindloss et al., 1972). The results showed Gamharia
reduced light supply in water and suppressed chaur (0.57±0.04) progressing towards eutrophic
phytoplankton development which untimely leads to low condition.
production.
Respiration as percentage of GPP
Community respiration
Respiration as percentage of gross may be as a measure
Respiration rate did not show much difference between the of eutrophic nature (Ganff and Horne 1975). This percent
lakes ranged from 0.428 g C m-2d-1 to 2.017 g C m-2d-1 at was really determined in previous studies, however, in this
Tarawe chaur and 0.489 g C m-2d-1 to 1.475 g C m-2d-1 at study it ranged from 20.23% to 49.23% at Tarawe chaur
Gamharia chaur. Mean respiration rate was 1.065±0.329 and 22.11% to 49.53% at Gamharia chaur, with mean
g C m-2d-1 and 1.009±0.275 g C m-2d-1 (Table 2). value of 34.46±8.05% and 42.79±4.40% (Table 2). Some
Respiration rate exhibited seasonal variability, high in workers reported the respiration as percentage of gross
summer might be due to greater microbial metabolisms, 20% to 45% in tropical estuary (Qasim et al., 1969) and
while low during winter could be due to the low 5.55% to 31.94% in fresh water body (Ahmad and Singh,
temperature and poor sun’s light affects rate of 1987). Variation in respiration as percentage of gross was
photosynthetic efficiency (Ahmad and Singh, 1987). Some seen, highest in monsoon and lowest in winter. Respiration
workers reported high respiration rate in winter and higher than 40% of gross production is characteristic of
moderate during flood season in bor-beel and the high in eutrophication (Ganf, 1972). The data obtained indicate
monsoon and low during autumn in beels of Assam eutrophic conditions at Gamharia chaur.
(Hazarika, 2010). Primary production rate in this study
exceeds respiration, it showed that lakes have autotrophic
environments. High respiration at Tarawe chaur could be CONCLUSIONS
due to unpredictable nature of heterotrophic organisms.
Respiration showed significant (p>0.01) positive The study highlighted phytoplankton productivity status
correlation with water temperature (r=0.847) and BOD and water quality in floodplain lakes of north Bihar, India.
(r=0.614) and significant negative correlation with Results show that floodplain lakes were highly productive
carbonate (r=-0.592) at Tarawe chaur while, it showed ecosystems as sufficient organic material is synthesized
significant (p>0.01) positive correlation with water for rising and supporting aquatic life and boosting fishery
temperature (r=0.834), phosphate (r=0.645), BOD production. Phytoplankton productivity was affected by the
(r=0.591) and bicarbonate (r=0.694), and significant interactions of a number of factors, like light, photoperiod
negative correlation with pH (r=-0.572) and carbonate (r=- and temperature. Water quality variables were interrelated
0.720) at Gamharia chaur (Table 3). and have profound effects on primary productivity. Primary
productivity showed close links with seasonal flooding.
NPP/GPP ratio

The ratio of NPP/GPP should approach unity in a healthy ACKNOWLEDGEMENTS


population, if, respiration is 5% to 10% of the total
photosynthesis (Ketchem et al., 1958). If this ratio is zero The authors would like to thank the Principal (B.D. College,
it shows poor physiological state of producer organisms Magadh University, Patna), and the Department of
due to nutrient deficiency. In the present study, NPP/GPP Zoology for providing necessary facilities for this work.
ratio was almost similar in both lakes ranged from 0.51 to
0.80 at Tarawe chaur and 0.50 to 0.79 at Gamharia chaur.
Mean ratio was 0.64±0.08 and 0.57±0.04 (Table 2). Similar REFERENCES
ratio was reported from floodplain lakes of Bihar (Palui and
Jha, 2003). NPP/GPP ratio of 0.5 g O 2/m2/day is good for Ahmad SH, Singh AK (1987). Seasonal fluctuations of
water body (Odum, 1971). NPP/GPP ratio was generally primary production and fish yield in Mangle’s tank,
less than one reflects that both lakes were productive. Patna City (Bihar). Geobios, 14: 62-66.
Ratio value was almost similar in lakes might be due to APHA (1989). Standard Methods for the Examination of
similarity in geographical location, topography and Water and Wastewater. 19th edn. APHA, AWWA,
catchment features, but, a little variation could be due to WPCF, Washington DC, USA.
The Contribution of Phytoplankton to the Primary Production in Floodplain Lakes (Chaurs) of North Bihar, India
Int. J. Ecol. Devel. Res. 048

Banerjee TC, Chattopadhyaya C (2008). Water Symposium. Can. Spec. Publ. Fish. Aquat. Sci. Ottawa,
temperature and primary production in the euphotic Canada 106, pp. 110-127
zone of a tropical shallow freshwater lake. Asian J. Exp. Ketchem BH, Ryther JH, Yentsch CS, Crwin N (1958).
Sci. 22(1): 103-108. Productivity in relation to nutrients. Rapp. Proc. Verb.
Baruah PP (2003). Primary productivity status of a Cons. Prem. Int. Explor. Metr. 144: 132-140.
reclaimed ox-bow beel of middle Assam. Geobios, McConnell WJ, Lewis S, Olson JE (1988). Gross
30(1): 49-52. photosynthesis as an estimator of potential fish
Bindloss M E, Holden A V, Balley Watts A E, Smith I R production. Trans. Amer. Fish. Soc. 106: 417- 423.
(1972). Phytoplankton primary production, chemical Moundiotiya C, Sisodia R, Kulshreshtha M, Bhatia AL
and physical conditions in Lake Leven. In: Kajak Z, (2004). A case study of the Jamwa Ramgarh wetland
Hillbricht-Ilkowska A, eds. Productivity problems in with special reference to physico-chemical properties of
freshwater. Polish Science Publication, Warsaw. pp. water and its environs. J. Environ. Hydrol. 12: 1-7.
639-659. Mukherjee A, Suresh VR, Mitra K (2006). Floodplain
Chaudhuri AB (2007). Endangered Wetlands. Daya wetlands of Ganga and Brahma-putra river systems:
publishing House, Delhi. p. 292. Status and sustainable fisheries development. In: Vass
Dash S, Patra AK, Adhikari S (2011). Primary productivity KK, Mitra K, Suresh VR, Katiha PK, Shrivastava NP,
of Kharasrota river (India). J. Ecophysiol. Occup. Hlth. eds. Proceeding of the national seminar on
11: 219-225. management challenges in fisheries of river and
Datta S (2003). Net primary production of phytoplankton in associated ecosystem: Issue and strategies, Inland
some tropical wetlands. Environ. Eco. 21: 6-9. Fisheries Society of India, Barrackpore, WB, pp. 164-
Davison IR (1991). Environmental effects on algal 183.
photosynthesis: temperature. J. Phycol. 27: 2-8. Odum EP (1971). Fundamentals of Ecology. 2nd edn.
Gaarder T, Gran HH (1927). Investigations of the W.B. Saunders Company, Philadelphia & London, p.
production of plankton in theOslo Fjord. Rapport et 574.
proces-verbaux desreunions. Conseil permanent Oglesby RT (1977). Relationships of fish yield to lake
international pour l'exploration de la mer. 42: 1-31. phytoplankton standing crops, production and
Ganesan L, Khan RA (2008). Studies on the ecology of morphometric-edaphic factors. J. Fish. Res. Bd Can.
zooplankton in a floodplain wetland of West Bengal, 34: 2271-2279.
India. In: Sengupta M, Dalwani R, eds. Proceedings of Palui D, Jha BC (2003). Productivity trends in two
Taal 2007, The 12th World Lake Conference, Jaipur, floodplain wetlands of Bihar. In: Sugunan VV, Vinci GK,
Rajasthan, India, pp. 67-73. Katiha PK, Das MK, eds. Fisheries Enhancement in
Ganf GG (1972). Regulation of net primary production in Inland Water: Challenge Ahead. Proceeding of the
Lake George, Uganda, East Africa. In: Kajak Z, Hill National Symposium Inland Fisheries Society of India,
Bright Illkowska A, eds. Productivity Problem in Fresh Barrackpore WB, pp. 87-94.
Water. Pol. Acad. Sci. Warsaw. Qasim SZ, Wellershaus S, Bhattathiri PMA, Abidi SAH
Ganf GG, Horne AJ (1975). Diurnal stratification, (1969). Organic production in a tropical estuary. Proc.
photosynthesis and nitrogen fixation in a shallow Indian Acad. Sci. 69(B): 51-94.
equatorial lake (Lake George, Uganda). Fresh. Wat. Robertson AI, Bacon P, Heagney G (2001). The
Biol. 5(1): 13-39. responses of floodplain primary production to flood
Hazarika S (2010). The study of the impact of flood in the frequency and timing. J. Appl. Ecol. 38(1): 126-136.
wetlands of Assam, North Eastern Region of India. The Rogers K, Ralph TJ (2010). Floodplain Wetland Biota in
Bioscan, 1: 269-281. the Murray-Darling Basin: Water and Habitat
Helbling EW, Villafañe VE (2009). Phytoplankton and Requirements. CSIRO Publishing, Australia, p. 348.
primary production. In: Safran P, eds. Fisheries and Sarma D, Das J, Dutta A (2013). Ecology of two riverine
Aquaculture, Vol. 5, Encyclopedia of Life Support wetlands of Goalpara district, Assam in relation to
Systems (EOLSS) developed under the Auspices of the plankton productivity. International journal of Applied
UNESCO, EOLSS Publishers, Oxford, pp. 206-226. Biology and Pharmaceutical Technology, 4(4): 219-
Hubas C, Davoult D, Cariou T, Artigas LF (2006). Factors 225.
controlling benthic metabolism during low tide along a Sarma D, Dutta A, Choudhury M (2007). Limnology and
granulometric gradient in an intertidal bay (Roscoff fisheries of Urpodbeel, Goalpara, Assam. J. Inland
Aber Bay, France). Mar. Ecol. Prog. Ser. 316: 53-68. Fish. Soc. India, 39(1): 51-54.
Jhingran VG, Natrajan AV, Banerjee SM, David A (1969). Sharma BK (2010). Phytoplankton diversity of two
Methodology on reservoir fisheries investigation in floodplain lakes (Pats) of Manipur (N.E. India). J.
India. Bull. Central Inland Fisheries Research Institute, Threat. Taxa, 2: 1273-1281.
Barrackpore, WB, 12: 1-109. Singh AK, Singh DK (1999). A comparative study of the
Junk WJ, Bayley PB, Sparks RE (1989). The flood pulse phytoplanktonic primary production of river Ganga and
concept in river: Floodplain systems. In: Dodge DP, ed. pond of Patna (Bihar), India. J. Environ. Biol. 26: 263-
Proceedings of the International Large River 270.
The Contribution of Phytoplankton to the Primary Production in Floodplain Lakes (Chaurs) of North Bihar, India
Singh et al. 049

Sreenivasan A (1964). The limnology, primary production Ziauddin G, Chakraborty SK, Jaiswar AK, Bhaumik U
and fish production in a tropical pond. Limnol. (2013). Productivity study in relation to temperature and
Oceanogr. 9(3): 391-396. transparency in the euphotic zone of selected tropical
Sugunan VV, Bhattacharjya BK (2000). Ecology and freshwater floodplain wetlands of West Bengal. The
Fisheries of Beelsin Assam. Bulletin No. 104. Central Ecoscan, 7(3-4): 101-107.
Inland Fisheries Research Institute, Barrackpore, WB,
p. 65.
Sugunan VV, Bhattacharjya BK, Hassan MA (2000).
Ecology and Fisheries of Beelsin West Bengal. Bulletin
No.103. Central Inland Fisheries Research Institute, Accepted 17 March 2018
Barrackpore, WB, p. 82.
Trivedy RK, GoelPK, (1986). Chemical and Biological Citation: Singh AK, Kumari R, Kumar A (2018). The
Methods for Water Pollution Studies. Environmental Contribution of Phytoplankton to the Primary Production in
Publications, Karad, India, p. 217. Floodplain Lakes (Chaurs) of North Bihar, India.
Vass KK, Langer RK (1990). Changes in primary International Journal of Ecology and Development
production and trophic status of a Kashmir ox-bow lake. Research, 4(1): 044-052.
J. Inland Fish. Soc. India, 22(1-2): 43-51.
Vinci GK, Mitra K (2000). Environmental issues and
sustainable fish production from floodplain lakes of
Ganga basin. In: Sinha M, Jha BC, Khan MA, eds.
Copyright: © 2018 Singh et al. This is an open-access
Environmental Impact Assessment of Inland Waters for
Sustainable Fisheries Management and Conservation article distributed under the terms of the Creative
of Biodiversity. Central Inland Capture Fisheries Commons Attribution License, which permits unrestricted
use, distribution, and reproduction in any medium,
Research Institute, Barrackpore, WB, pp. 67-75.
provided the original author and source are cited.
Wetzel RG, Likens GE (1979). Limnological Methods.
W.B. Saunders Co., Philadelphia, p. 357.

The Contribution of Phytoplankton to the Primary Production in Floodplain Lakes (Chaurs) of North Bihar, India
Int. J. Ecol. Devel. Res. 050

APPENDIX

Fig. 1: Geographical location of sampling sites.

Fig. 2: Variations of Gross Primary Production.

The Contribution of Phytoplankton to the Primary Production in Floodplain Lakes (Chaurs) of North Bihar, India
Singh et al. 051

Fig. 3: Variations of Net Primary Production.

Fig. 4: Variations of Community Respiration.

Table 1: Selected physico-chemical variables of floodplain lakes (Minimum/Maximum, mean and standard
deviation).

Parameters Tarawe chaur Gamharia chaur


Min/Max Mean ± SD Min/Max Mean ± SD
Water temperature 18.5 - 35.3 27.85 ± 5.69 18.3 - 33.8 26.82 ± 4.48
Transparency 9.9 - 59.6 34.82 ± 17.10 10.5 - 44.3 27.92 ± 11.56
Electrical conductivity 89.6 - 227.4 160.32 ± 43.39 109.3 - 461.8 284.04 ± 108.24
pH 6.9 - 8.3 7.55 ± 0.41 6.2 - 7.7 6.94 ± 0.47
Dissolved oxygen 5.2 - 8.9 6.97 ± 1.14 4.9 - 7.4 6.08 ± 0.84
Free CO₂ 4.7 - 9.4 7.05 ± 3.32 5.2 - 11.8 8.63 ± 3.30
Carbonate alkalinity 11.0 - 16.1 13.27 ± 1.60 12.8 - 22.1 16.73 ± 3.17
Bicarbonate alkalinity 107.6 - 159.5 131.18 ± 17.29 121.7 - 215.7 176.26 ± 32.30
Calcium 18.6 - 29.5 24.10 ± 3.68 10.8 - 26.9 18.92 ± 4.82
Magnesium 6.0 - 9.9 7.75 ± 1.26 7.1 - 13.4 10.30 ± 2.10
Chloride 6.3 - 16.2 11.80 ± 3.32 17.4 - 35.7 27.31 ± 5.73
Nitrate nitrogen 0.11 - 0.41 0.28 ± 0.11 0.33 - 0.70 0.51 ± 0.11
Phosphate phosphorus 0.06 - 0.20 0.12 ± 0.04 0.09 - 0.21 0.15 ± 0.04
BOD 1.4 - 2.9 2.29 ± 0.49 2.1 - 6.1 4.35 ± 1.40
All the parameters are expressed in mg/l, except pH, temperature (oC), transparency (cm), electrical conductivity (µ
mho/cm).

The Contribution of Phytoplankton to the Primary Production in Floodplain Lakes (Chaurs) of North Bihar, India
Int. J. Ecol. Devel. Res. 052

Table 2: Primary productivity parameters of floodplain lakes.


Parameters Tarawe chaur Gamharia chaur
Range Mean ± SD Range Mean ± SD
Gross Primary Production 1.849 - 4.994 2.872 ± 1.11 1.319 -3.965 2.395 ± 0.78
Net Primary Production 1.037 - 3.382 1.854 ± 0.84 0.728 -2.621 1.385 ± 0.54
Community respiration 0.491 - 1.816 1.065 ± 0.33 0.591 -1.475 1.009 ± 0.28
NPP: GPP ratio 0.51 - 0.76 0.64 ± 0.08 0.50 - 0.66 0.57 ± 0.04
Respiration as % of gross 24.18 - 49.23 34.46 ± 8.05 33.9 - 49.53 42.79 ± 4.40

42.790 ± 4.40
GPP, NPP and CR values in g C/m 2/day

Table 3: Correlation co-efficient (r) values between primary productivity and water quality variables.
Parameters Tarawe chaur Gamharia chaur
GPP NPP CR GPP NPP CR
Water Temperature 0.674* 0.516* 0.847* 0.543* 0.324 0.834*
Transparency - 0.069 0.098 - 0.366 - 0.123 0.088 -0.536*
Sp. Conductivity. 0.010 0.163 - 0.322 - 0.048 0.160 - 0.480
pH - 0.292 - 0.144 - 0.519* - 0.144 0.075 -0.572*
Dissolved oxygen - 0.229 - 0.098 - 0.440 - 0.148 0.057 -0.541*
Free carbon dioxide - 0.341 - 0.185 - 0.700 - 0.425 - 0.428 - 0.126
Carbonate alkalinity - 0.630* - 0.638* - 0.592* - 0.511 - 0.342 -0.720*
Bicarbonate alkalinity 0.113 - 0.059 0.412 0.377 0.172 0.694*
Calcium 0.604* 0.655* 0.359 0.559* 0.552* 0.386
Magnesium 0.752* 0.797* 0.563* 0.566* 0.540* 0.432
Chloride 0.619* 0.682* 0.380 0.466 0.511 0.212
Nitrate-nitrogen 0.168 0.012 0.454 0.153 - 0.066 0.576*
Phosphate-phosphorus 0.212 0.059 0.459 0.290 0.081 0.645*
Biochemical oxygen demand 0.372 0.211 0.614* 0.192 - 0.023 0.591*
* = Significant at p >0.01

The Contribution of Phytoplankton to the Primary Production in Floodplain Lakes (Chaurs) of North Bihar, India

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