CHAPTER II PRIMARY PRODUCTIVITY- NET AND GROSS
Page 60
INTRODUCTION
The flow of energy through any ecosystem starts with the fixation
of sunlight by plants and other autotrophic organisms. In this way the
plant accumulates energy and this energy is called primary production.
The rate at which this energy accumulates is called primary productivity.
The total energy accumulated is gross primary production; however,
since plants use some of this energy themselves, it is not all available for
the food web (Mitsch and Gosselink, 1993).
According to Vollenweider (1974), estimation of primary production
estimation is concerned with "evaluation of the capacity of an ecosystem
to build up, at the expense of external energy (radiant and chemical),
primary organic compounds for transformation and flow to a higher level
trophic system". It measures the trophic status and changes in trophic
characteristics, over time, of open water systems.
The fundamental process involved in primary production is usually
expressed by the following equation:
6CO 2 + 6H2 + Light energy = C6 H12O6 +6O 2
Concepts of Productivity:-
There are successive steps in the process of primary productivity-
Gross Primary Productivity: - It is the total rate of photosynthesis
including the organic matter used up in respiration during the
measurement period. This is also known as total photosynthesis or
total assimilation.
Net Primary Productivity: - It is the rate of storage of organic
matter in plant tissues in the excess of the respiratory use by the
Page 61
plants during the measurement period. This is also called as
apparent photosynthesis or net assimilation.
Net Community Productivity: - It is the rate of storage of organic
matter not used by heterotrophs during the growing season or
year. Actually this is the net primary production minus the period
of consideration.
Net Production Efficiency: - The ratios measure the efficiency with
which an organism converts assimilated energy into primary or
secondary production.
The early investigations done (Datta, 1984; Wondie et al, 2007) on
lakes in different parts of the globe indicate that the physico-chemical
properties of water have a direct relation with the primary production.
Inflow and outflow of water, nutrient loading and entry of harmful
materials (pollutants) of any kind, all have a distinct, both immediate
and long term, effects on the metabolic rates. Hence measurements of
the rate of primary production can be used as an important bioassay
method for pollution studies. Primary production depends on the density
of various planktonic groups, availability of light, and changes in
environmental factors such as temperature, meteorological, hydrological,
nutritional and biological characteristics. It may vary greatly due to local
conditions such as morphology, water currents, local inflows of rivers, or
nature of the substratum (Prabhakar et al., 2009).
The estimation of primary productivity of an ecosystem is essential
to understand its food chains and food web. The daily and seasonal
carbon flow in the system forms the base of annual food pyramid and
can be used to estimate production of at higher tropic levels. The
evaluation of primary production of an ecosystem is one of the important
factors to form estimates of potential fish yield. Photosynthesis is the
Page 62
fundamental process involved in primary productivity. Primary
production may be the most important biological phenomenon in nature
on which the entire diverse array of life depends, either directly or
indirectly. It is the driving force for all metabolic activities in the
biosphere. It also shows the ability of an area to support the growth of
biological population, including fish population. To estimate the total
bioactivity of a reservoir it is necessary to determine the magnitude of
primary production (Prasad, 1990). The study of primary production in
lakes is fundamental to understanding both water quality and fisheries
(Wondie et al, 2007).
Primary production is influenced by a combination of physical and
biological factors: sunlight, lake morphometry, lake chemistry, nutrient
cycling, mixing, and consumer community composition. Sunlight
provides the energy for photosynthesis to occur, and thus is critical for
primary production. Primary production is limited to depths to which
sunlight can penetrate, regardless of any other factors (Wetzel, 2001).
Shallow lakes by area are often more productive than deep lakes in part
due to nutrient recycling from sediments (Flanagan and McCauley, 2008)
and the extent of attached macrophytes growth (Meding and Jackson,
2003).
The overall productivity of a water body can easily be deduced from
its primary productivity, which forms the backbone of the aquatic food
chain (Ahmed and Singh, 1989). The concept of primary productivity is
related to the ideas of energy flow in ecosystem (Odum, 1971). Primary
productivity of aquatic ecosystem gives the quantitative details regarding
energy fixation and its availability to support bioactivity of the total
system. Productivity of lakes depends on the presence of plankton
biomass (Joseph and Shanthi, 2010).
Page 63
Lakes are one of the important sources of potential production in
the world. Physical, chemical, and biological aspects influence primary
productivity directly and the fish production indirectly (Chinnaiah and
Madhu, 2008). Diversity in the distribution, abundance, and vari ations
in the biotic factors provides information of energy turnover in aquatic
ecosystem. Estimation of primary productivity of the aquatic system, are
adversely affected by anthropogenic activity servers as an important tool
in standing the effect of those activities in the ecosystem. Rates of
primary productivity indeed have been included as a component of many
trophic state assessment frameworks for freshwater and marine
ecosystems worldwide (Rodhe, 1970; Andersen et al., 2006). Nearly every
abiotic and biotic characteristic of the reservoir system influences the
resultant primary productivity, often rapidly in response to diel,
seasonal, or irregular periodicities of these characteristics unlike
temperate lakes where temperature and light intensity are the chief
limiting factors, biological productivity in tropical lakes are largely
controlled by nutrient regimes (Kumar, 1990).
The primary productivity plays an important role in the
penetration, absorption and distribution of light & heat and density
stratification of the lakes (Cole, 1983). The primary production is
dependent on physical condition such as temperature, light, and
nutrients (Davis, 1955). Productivity of lakes depends upon a variety of
factors such as the distance between the photosynthetic and
decomposition zone and volume of the water available (Tonapi, 1980).
Primary productivity gives information related to the amount of energy
available to support bio-activities of the system (Vollenweider, 1974).
Primary productivity has been measured for aquatic ecosystem by
several workers. Singh and Desai (1980) estimated the rates of primary
Page 64
production on Rihand reservoirs in U.P. Palahiappan et al (1981)
recorded the primary productivity of two rock polls in Salem, Tamilnadu.
Datta et al (1984) have assessed the primary productivity in relation to
some physico chemical properties of a freshwater pond in Kolkata.
Ayyappan and Gupta (1985) opined that the production of Ramasamudra
tank from coastal Karnataka was controlled by several hydrobiological
factors. Singh (1986) has determined the primary productivity of two
lakes at Pune in relation to environmental parameters. Sharma and
Sahai (1988) have conducted work on primary productivity and energy
flow in upper Lake of Bhopal and observed a seasonal variation in
primary productivity with maxima in winter and minima in summer.
Shukla and Bais (1990) observed a correlation between phytoplankton
biomass and productivity with physico chemical parameters of Bila
reservoirs, Shahgarh, Madhya Pradesh. Vijaykumar and Paul (1990)
reported on primarily productivity of different water bodies of Gulberga,
Karnataka. Patil and Sahu (1993) studied on primary production of
Rengali reservoirs, Orissa. Vijaykumar (1994) reported on seasonal
variation in primary productivity of tropical pond in Gulberga.
Vasantkumar et al (1996) studied on impacts of dairy effluents on
primary production in freshwater pond at Gulberga, Karnataka. Singh
and Sharma (1999) carried out hydrobiological and primary productivity
in fish pond manure with different organic manures. Vijaykumar et al
(2000) studied on seasonal variation in primary productivity of Gobbur
tank, Gulberga. Prakash (2001) carried out a seasonal dynamics of
zooplankton and primary productivity at Balarampur (U.P). Shukla and
Pawar (2001) estimated primary productivity of Govindgarh Lake, Rewa,
(M.P). Yeragi et al (2002) estimated the gross primary production of
urban creek in Thane. Sukumaran (2002) studied on primary production
dynamics of a perennial tank in Bangalore. Sobha et al (2003) made an
effort to analyze primary productivity of Paravar canal. Sivakumar and
Page 65
Karuppasamy (2008) studied on factors affecting productivity of
phytoplankton in a reservoir of Tamilnadu, India. Joseph and Shanthi
(2010) studies on assessment of the primary productivity of
Muvattupuzha River, Kottayam, Kerala. Mohan et al (2010) observed
seasonal variations in the phytoplankton diversity and primary
productivity of Pechiparai reservoir, Kanyakumari. Patil and Chavan
(2010) have reported primary productivity of three lakes from Sangli
district. Bhosle et al (2010) reported on seasonal variations in occurrence
of phytoplankton and primary productivity of some selected lakes in
Maharashtra. Chinnaiah and Madhu (2010) carried out assessment of
primary productivity of Darmasagar Lake in Adilabad, Andhra Pradesh.
Vasantkumar and Vijaykumar (2011) studied on diurnal variation of
physico chemical properties and primary productivity of phytoplankton
in Bheema River, Gulberga, Karnataka.
The present study has been undertaken to analyse the net and
gross primary productivity of two freshwater lakes namely Mombatta and
Kagzipura, in Aurangabad district, Maharashtra.
Page 66
MATERIALS AND METHODS
STUDY AREA
Kagzipura lake (latitude 190 57’ N and longitude 750 15’ E) is
located near Kagzipura village, Tal. Khultabad 16 km away from
Aurangabad city whereas Mombatta lake is situated in Daulatabad valley
(latitude 190 57’ 42” N and longitude 750 13’ 24” E) near Daulatabad
village, Tal. Aurangabad, 15 km away from Aurangabad. Both lakes are
used for irrigation and aquaculture purposes.
The Primary productivity of Mombatta and Kagzipura is
determined by using standard “Light and Dark bottle” method of Gardner
and Gran (1927) at an interval of 15 days in every month for a period of
two years from October 2008 to September 2010.
The method of Gardner and Gran (1927) method is slightly
modified by Vollenweider et al (1974) and Wetzel and Likens (1991) to
make it more suitable. A set of one light and one dark bottle with a
capacity of 200ml were filled with surface water and closed tightly and
the dark bottle was covered with black aluminum foil to prevent the
penetration of light. Both bottles were suspended in the lake at level 10
cm deep from which the original water was taken and exposed to natural
light. At the time of keeping these two light and dark bottles in water
their maintain the difference of 30 to avoid the self-shading effect. The
dissolved oxygen was determining using the sample from third (initial)
bottle. The primary productivity study carried out after 7 to 9 AM. The
time of exposure (incubation period) in the present study was for the
period of 2 hrs. After completion incubation period the two set of light
and dark bottles were fixing the samples with magnous Sulphate and
alkali iodide at the site of the study area then transferred to the lab, for
Page 67
further estimation. The dissolved oxygen is determined by the initial
bottle and light and dark bottle (after 2 hour incubation) by Winkler’s
method. The estimation of dissolved oxygen is done by Winkler’s method
(Wetzel and Likens, 1991) described in chapter first. The observed Net
primary productivity (NPP), gross primary productivity (GPP) and
Community respiration (CR) in mg/l/hr were converted into gC/m3/hr
by multiplying these values with a factor 0.375 as suggested by Benton
and Werner (1972).
The Gross and Net primary production and community respiration
was estimated by using following formulae of Wetzel and Likens (1991):
Gross primary productivity (GPP): gC/m3/hr = DL-DD X 0.375
Hr
Net primary productivity (NPP): gC/m3/hr = DL-DI X 0.375
Hr
Community respiration (CR): gC/m3/hr = DI-DD X 0.375
Hr
Net Production Efficiency (NPE): % = NPP × 100
GPP
Respiration (% of GPP): % = CR × 100
GPP
Where,
DL = Dissolved oxygen in light bottle in mg/l.
DD = Dissolved oxygen in dark bottle in mg/l.
DI = Dissolved oxygen in initial bottle in mg/l.
Hr = Duration of exposure (incubation period) in hrs.
0.375 = Respiratory quotient.
Page 68
Procedure:
1. Gross Primary Productivity:
Gross primary productivity is determined by with the help of above
said formula. In which, the value of dissolved oxygen obtained from light
bottle is minus from the value of dissolved oxygen obtained from dark
bottle. Then these values are divided by duration exposure in hours and
then it multiplied by a factor (0.375). The values are expressed in
gC/m3/hr.
2. Net Primary Productivity:
Net Primary productivity is determined by with the help of above
said formula. In which, the value of dissolved oxygen obtained from light
bottle is minus from value of dissolved oxygen obtained from initial
bottle. Then these values are divided by duration exposure in hours and
then it multiplied by a factor (0.375). The values are expressed in
gC/m3/hr.
3. Community Respiration:
Community respiration is determined by using above said formula.
In which, the value of dissolved oxygen obtained from initial bottle minus
the value of dissolved oxygen obtained from dark bottle. Then these
values are divided by duration exposure in hours and then it multiplied
by a factor (0.375). The values are expressed in gC/m3/hr.
Statistics was applied to determine the correlation coefficient
(Mungikar, 2003) between Physico-chemical water parameters and
zooplanktons with primary productivity.
Page 69
RESULT
MOMBATTA LAKE
PRIMARY PRODUCTIVITY
Monthly data of Primary Productivity is recorded as Gross primary
productivity, net primary productivity, Community respiration, Net
production efficiency and Respiration (% of GPP) from Mombatta Lake
during October 2008 to September 2009 is depicted in Table 1 from
October 2009 to September 2010 and in Table 2. Average of monthly
record of Primary Productivity during the period of October 2008 to
September 2010 is given in Table 3 and Fig 1 to 5. Seasonal changes in
Primary Productivity during October 2008 to September 2009 and
October 2009 to September 2010 are given in Table 4. Average of
seasonal record of Primary Productivity during October 2008 to
September 2009 and October 2009 to September 2010 is given in Table 5
and Fig 6 to11. Simple correlation coefficient of Primary Productivity is
given in Table 6.
Gross Primary Productivity (gC/m3/hr):
Gross primary productivity found minimum in the month of
September (0.53 ± 0.0.03) and maximum in May (1.82 ± 0.06) as given in
Table 3 and Fig 1. Average seasonal record of Gross primary productivity
in Mombatta Lake showed minimum in monsoon season (0.66 ± 0.17)
and maximum in summer season (1.65 ± 0.15) as given in Table 5 and
Fig 6.
Statistical analysis of data collected from Mombatta Lake revealed
that Gross primary productivity is positively correlated (P<0.01) with Net
primary productivity and (P<0.05) Community respiration whereas,
Page 70
negatively correlated (P>0.05) with Net production efficiency and
Respiration (Table, 6).
Net Primary Productivity (gC/m3/hr):
In Mombatta Lake, minimum Net primary productivity was
observed in the month of September (0.50 ± 0.03) and maximum in the
month of October (1.67 ± 0.01) [Table 3 and Fig 2]. Average seasonal
record of Net primary productivity in Mombatta Lake showed minimum
in monsoon season (0.60 ± 0.17) and maximum in summer season (1.45
± 0.23) [ Table 5 and Fig 7].
Statistical analysis of data collected from Mombatta Lake revealed
that Net primary productivity is positively correlated (P<0.01) with Gross
primary productivity whereas, negatively correlated (P>0.05) with
Respiration and no correlation with Community respiration and Net
production efficiency (Table, 6).
Community Respiration (gC/m3/hr):
In Mombatta Lake, minimum Community respiration was observed
in the month of September (0.03 ± 0.01) and maximum in the month of
May (0.25 ± 0.02) as given in Table 3 and Fig 3. Average seasonal record
of Community Respiration in Mombatta Lake showed minimum in
monsoon season (0.06 ± 0.01) and maximum in winter season (0.20 ±
0.07) as given in Table 5 and Fig 8.
Statistical analysis of data collected from Mombatta Lake revealed
that community respiration is positively correlated (P<0.05) with Gross
primary productivity whereas, negatively correlated (P>0.05) with Net
production efficiency and no correlation with Net primary productivity
and Respiration (Table, 6).
Page 71
Net Production Efficiency (gC/m3/hr):
In Mombatta Lake, minimum Net production efficiency was
observed in the month of March (84.25 ± 0.18) and maximum in the
month of October (95.98 ± 0.31) [Table 3 and Fig 4]. Average seasonal
record of Net production efficiency in Mombatta Lake showed minimum
in monsoon season (87.74 ± 3.37) and maximum in winter season (95.39
± 0.60) [Table 5 and Fig 9].
Statistical analysis of data collected from Mombatta Lake revealed
that net production efficiency is negatively correlated (P>0.05) with gross
primary productivity, community respiration and respiration whereas, no
correlation with net primary productivity. (Table, 6).
Respiration (gC/m3/hr):
In Mombatta Lake, minimum Respiration was observed in the
months of November (0.06 ± 0.01) and maximum in June (5.81 ± 0.03)
[Table 3 and Fig 5]. Average seasonal record of Respiration in Mombatta
Lake showed minimum in summer season (1.04 ± 0.79) and maximum in
monsoon season (2.97 ± 2.27) [Table 5 and Fig 10].
Statistical analysis of data collected from Mombatta Lake revealed
that net production efficiency is negatively correlated (P>0.05) with gross
primary productivity, net primary productivity and net production
efficiency and no correlation with community respiration (Table, 6).
Page 72
KAGZIPURA LAKE
Primary Productivity (gC/m3/hr):
Monthly record of Primary Productivity recorded as Gross primary
productivity, net primary productivity, community respiration, net
production efficiency and respiration (% of GPP) from Kagzipura Lake
during October 2008 to September 2009 is depicted in Table 7 and from
October 2009 to September 2010 in Table 8. Average of monthly record
of Primary Productivity during the period of October 2008 to September
2010 is given in Table 9 and Fig 1 to 6. Average of seasonal record of
Primary Productivity during October 2008 to September 2009 and
October 2009 to September 2010 are given in Table 10. Seasonal
changes in Primary Productivity during October 2008 to September 2009
and October 2009 to September 2010 given in Table 11. Correlation
coefficient of Primary Productivity is given in Table 11 and Fig 7 to 11.
Gross Primary Productivity (gC/m3/hr):
Gross primary productivity was observed minimum in the month of
September (1.02 ± 0.16) and maximum in October (3.32 ± 0.27) as given
in Table 7 and Fig 1. Average seasonal record of Gross primary
productivity in Kagzipura Lake showed minimum in monsoon season
(1.19 ± 0.78) and maximum in summer season (2.50 ± 0.90) as given in
Table 11 and Fig 6.
Statistical analysis of data collected from Kagzipura Lake revealed
that Gross primary productivity is positively correlated (P<0.01) with Net
primary productivity and negatively correlated (P>0.05) Net production
efficiency and no correlation with community respiration and respiration
(Table, 12).
Page 73
Net Primary Productivity (gC/m3/hr):
In Kagzipura Lake, minimum Net primary productivity was
observed in the month of August (1.06 ± 0.01) and September (0.50 ±
0.03) whereas, maximum in the months of October (3.15 ± 0.01) and
November (3.12 ± 0.02) as given in Table 9 and Fig 2. Average seasonal
record of Net primary productivity in Kagzipura Lake showed that, it is
found minimum in monsoon season (1.12 ± 0.73) and maximum in
winter season (2.38 ± 0.88) given in Table 11 and Fig 7.
Statistical analysis of data collected from Kagzipura Lake revealed
that net primary productivity is positively correlated (P<0.01) with Gross
primary productivity and negatively correlated (P>0.05) Net production
efficiency and no correlation with Community respiration and
Respiration (Table, 12).
Community Respiration (gC/m3/hr):
In Kagzipura Lake, minimum Community respiration was observed
in the month of July (0.04 ± 0.01) and August (0.04 ± 0.01) and
maximum in the month of April (0.31 ± 0.01) as given in Table 9 and Fig
3. Average seasonal record of Community respiration in Kagzipura Lake
showed minimum in monsoon season (0.07 ± 0.09) and maximum in
summer season (0.23 ± 0.09) as given in Table and 11and Fig 8.
Statistical analysis of data collected from Kagzipura Lake revealed
that community respiration is positively correlated (P<0.05) with
respiration and negatively correlated (P>0.05) Net production efficiency
whereas no correlation with Gross primary productivity and Net primary
productivity (Table, 12).
Page 74
Net Production Efficiency (gC/m3/hr):
In Kagzipura Lake, minimum Net production efficiency was
observed in the month of April (83.88 ± 0.23) and maximum in August
(96.80 ± 0.14) as given in Table 9 and Fig 4. Average seasonal record of
Net production efficiency in Kagzipura Lake showed minimum in
summer season (89.16 ± 5.12) and maximum in winter season (95.64 ±
0.44) as given in Table 11 and Fig 9.
Statistical analysis of data collected from Kagzipura Lake revealed
that Net production efficiency is negatively correlated (P>0.05) with Gross
primary productivity and Net primary productivity, Community
respiration and Respiration (Table, 12).
Respiration (gC/m3/hr):
In Kagzipura Lake, minimum Respiration was observed in the
month of July (0.07 ± 0.003) and maximum in May (6.02 ± 0.92) as given
in Table 9 and Fig 5. Average seasonal record of Respiration in Kagzipura
Lake showed minimum in monsoon season (0.75 ± 0.67) and maximum
in summer season (2.29 ± 2.37) as given in Table 11 and Fig 10.
Statistical analysis of data collected from Kagzipura Lake revealed
that respiration is positively correlated (P<0.05) with community
respiration and negatively correlated (P>0.05) with net production
efficiency whereas no correlation with gross primary productivity and net
primary productivity (Table, 12).
Page 75
DISCUSSION
Primary production is the direct product of photosynthesis, and
primary productivity is the sum of all photosynthetic rates in an
ecosystem (Fee, 1998). Information on the primary production enables to
improve the understanding of food web relationship in aquatic ecosystem
(Kauer et al, 2009).
Changes in primary productivity have been causally linked to the
nutrient status of aquatic ecosystem for over a century and it has
recently recommended that measurement of primary productivity, being
a sensitive and accurate indicator of eutrophication and diagnostic tool
for assessing the metabolic status of any Lake (Smith, 2007). Similarly,
the ratio between the Net and Gross primary productivity would
approach unity when the respiration ranges between 5 to 10 percent of
Gross primary productivity in a healthy Lake (Ketcham et al., 1958).
Primary productivity gives information related to the amount of
energy available to support bioactivities of the system (Vollenweider,
1974). The estimation of primary productivity of an ecosystem is
essential to understand its food chains and food web. The daily and
seasonal carbon flow in the system forms the base of annual food
pyramid and can be used to estimate production at higher trophic level.
Lakes are one of the important sources of potential production in the
world. Physical, chemical and biological aspects influence primary
productivity directly and the fish production indirectly (Chinnaiah and
Madhu, 2010).
Page 76
Primary production is an important biological phenomenon in the
aquatic environment in which phytoplankton act as a primary producer,
their physiological activities greatly controlled by physicochemical
characters of the water body (Sahu et al,. 1995; Aravind Kumar, 1997).
Phytoplankton also serve as food for aquatic animals especially for fishes
and also they play an important role in ecological balance and quality of
the water (Pandey et al., 1994). Sharma and Sharma (1992) noted that
phytoplankton found in the water body as well as they may be used as
indicators of the water quality.
Shallow lakes (by area) are often more productive than deep lakes
in part due to nutrient recycling from sediments (Flanagan and
McCauley, 2008) and the extent of attached macrophyte growth (Meding
and Jackson, 2003). As lake surface area increases, the amount of
sunlight penetrating the water increases, as well as providing more area
for CO2 diffusion. The absolute abundance of critical nutrients such as
phosphorus, nitrogen and silica, are important determinants of primary
production, and producer biomass has been shown to increase along
increasing gradients of nutrient supply (Elser et al. 1988).
In any aquatic body primary productivity gives information relating
to the amount of energy available to support bioactivity of the system
(Vollenweider 1969). Estimation of primary productivity of the aquatic
systems, those are adversely affected by anthropogenic activities, serves
as an important tool in studying the effect of those activities on the
system. Several studies are available relating to the primary productivity
of different ponds, lakes and reservoirs in different parts of India (Verma
& Mohanty 1994).
Page 77
The reservoir ecosystems are intermediate between rivers and
natural Lakes in relation to morphology, hydrology, nutrients loadings
and cycling, and source of organic matter. Much of the primary
production within reservoir is by phytoplankton. Primary productivity is
most important biological phenomenon in nature, which involves the
trapping of radiant energy of sun, and its transformation into high
potential biochemical energy flow in a ecosystem. Understanding of
primary production becomes all the more essential in the evaluation of
the capacity of any ecosystem, including that of standing water bodies.
The primary productivity relates to the amount of organic matter
synthesized in certain space per unit term. Primary productivity can be
access as gross and net values. Gross primary production is the total
range of photosynthesis including organic matter used up in the
respiration in a given time while net productivity is the total amount of
chemical energy net after it has been utilized by plants for respiration.
Primary productivity has been used for potential index of productivity for
many diverse ecosystem of the world (Wetzel, 2001). Primary productivity
is concerned with the evaluation of the capacity of an ecosystem to the
synthesis of organic matter of high chemical potential. Primary
productivity in aquatic ecosystem mainly is controlled by interaction of
many factors like environmental and biotic factors and nutrient status of
the water body. Thus, this aspect has drawn the attention of numerous
hydrobiologists.
GROSS AND NET PRIMARY PRODUCTIVTY (gC/m3/hr):
Gross primary productivity is the total rate of photosynthesis
including the organic matter used up in respiration during the
measurement period. This is also known as total photosynthesis or total
assimilation. Net primary productivity is the rate of storage of organic
matter in plant tissues in the excess of the respiratory use by the plants
Page 78
during the measurement period. This is also called as apparent
photosynthesis or net assimilation.
In the present study, Gross primary productivity of Mombatta Lake
was minimum in the months of August and September whereas,
maximum in the months of April and May. In Kagzipura Lake, minimum
Gross primary productivity was observed in the months of August and
September whereas maximum in the months of October and November.
Average seasonal record of Gross primary productivity in Mombatta Lake
showed minimum in monsoon and maximum in summer season. Average
seasonal record of Gross primary productivity in Kagzipura Lake showed
minimum in monsoon and maximum in winter season.
In the present study, Net primary productivity of Mombatta and
Kagzipura Lake was minimum in the months of August and September
whereas maximum in the months of October and November. Average
seasonal record of Net primary productivity in Mombatta Lake showed
minimum in monsoon season and maximum in winter season.
Mandal et al (1999) stated that the trend of fluctuations shows
that values of Gross primary productivity and Net primary productivity
increased gradually during winter and summer and decreased during
monsoon. The highest rate of productivity during summer may be due to
bright sunshine with high temperature, high phytoplankton density and
algal blooms. The monsoon lows could be attributed to the reduced
photoperiod coupled with low light intensity, temperature and scare
phytoplankton. Majagi and Vijaykumar (2005) from Karanja reservoir
near Byalhalli village of Bidar district reported high primary productivity
during summer season due to the high light penetration while low
Page 79
productivity during monsoon season because of the influx of the turbid
water to the reservoir.
Prabhakar et al (2009) from Khadakwasla reservoir of Pune
reported that the primary productivity maximum in winter and minimum
in monsoon season. Clear water surface, which permitted more light to
penetrate and lower water flow perhaps, accounted for the higher values
of primary productivity during winter. Addition of nutrients with runoff
water during monsoon rain and later clarity of water during this season
are responsible for high primary productivity during winter. Lower values
are observe during monsoon might be due to increased turbidity and
suspended silt content of water resulting from soil erosion from
surrounding hills. As a consequence penetration of light into the water,
the most essential factor for photosynthesis drooped sharply. Higher rate
of water flow and more depth of the reservoir are also responsible for low
primary productivity.
Patil and Chavan (2010) from three lakes of Sangli district
observed that productivity increased from winter and attains the peak in
summer and then declines in monsoon. Highest rate of productivity
during summer was probably due to bright sunlight and higher
temperature. In concluding remarks they found that these three lakes
have low values of primary productivity due to less availability of
nutrients. Joseph and Shanthi (2010) from Muvattupuzha river,
Kottayam, Kerala reported maximum primary productivity in the months
of April and May due to algal blooms. Sawant et al (2010) from Atyal
Pond in Gadhinglaj Tahsil, Dist. Kolhapur, Maharashtra, reported the
Productivity of lakes depends on presence of planktonic biomass.
Page 80
According to Koli and Ranga (2011) high values of primary
productivity was mainly due to sewage discharged, industrial influents,
agricultural runoff and other human activities by surrounding city
population. High values of productivity and nutrients also exposed its
eutrophic condition. They found highest values of primary productivity in
summer season due to high temperature, which enhances the release of
nutrients from sediments through bacterial decomposition. The excessive
amounts of nutrients along with higher temperature favor the maximum
growth of aquatic flora, which ultimately favors the primary productivity.
Such findings are supported to present study for Mombatta and
Kagzipura Lake.
The Kagzipura and Mombatta Lake show bimodal trend of primary
productivity with two clear peaks, first in the months of October and
second in May. The magnitude and higher values of primary productivity
suggest that Lake is entropic in nature. Similar findings are reported by
various authors. Prabhakar et al (2009) from Khadakwasla reservoir in
Pune. Chinnaiah and Madhu (2010) from Darmasagar Lake in Adilabad.
Similar bimodal pattern also observed by Mohan et al (2010) from
Pechiparai Reservoir in Kanyakumari district.
Rajput and Negi (2011) from Nainital and Bhimtal lakes of Kumaon
Himalaya of Uttarkhand state reported that a lake having dense
population of plankton indicting higher productivity and less plankton
concentration indicates low productivity. Less phytoplankton, plankton
density, nutrient status and deep water body is responsible for low
primary productivity of Mombatta Lake while Kagzipura Lake has during
winter and summer season rich population of planktons, high nutrient
load due to inflow of swage, human activities, brick factories, excessive
algal growth and macrophytes resulting in high productivity. Hence high
Page 81
productivity indicating the polluted and eutrophication of water body.
Similar results are also observed by Anjinappa (2002) and Das (2002).
Statistical analysis of data collected for Mombatta Lake revealed
that Gross primary productivity positively is correlated with Net primary
productivity and Community respiration whereas negatively correlated
with Net production efficiency and Respiration. Statistical analysis of
data collected for Kagzipura Lake revealed that Gross primary
productivity is positively correlated with Net primary productivity and
negatively correlated with Net production efficiency and no correlation
with Community respiration and Respiration.
Statistical analysis of data collected for Mombatta Lake revealed
that Net primary productivity is positively correlated with Gross primary
productivity whereas negatively correlated with Respiration and no
correlation with Community respiration and Net production efficiency.
Statistical analysis of data collected for Kagzipura Lake revealed that net
primary productivity is positively correlated with Gross primary
productivity and negatively correlated with Net production efficiency and
no correlation with Community respiration and Respiration.
Majagi and Vijaykumar (2005) from Karanja reservoir, Karnataka,
reported Gross primary productivity is positively correlated with Net
primary productivity, Community respiration, water temperature, pH,
dissolved oxygen, total alkalinity, chloride, Rotifera, Copepoda, and
Cladocera whereas, Net primary productivity is positively correlated with
Gross primary productivity, Community respiration water temperature,
pH, dissolved oxygen, total alkalinity chloride, Copepoda, ostracoda and
Rotifera.
Page 82
Rajput and Negi (2011) from Nainital Lake of Kumaon Himalaya of
Uttarkhand, reported that Gross primary productivity is positively
correlated with Net primary productivity, pH and water transparency and
negatively correlated with total alkalinity, dissolved solids, chlorides and
total hardness whereas Net primary productivity is positively correlated
with pH and Gross primary productivity whereas negatively correlated
with water temperature, air temperature, total dissolved solids, chlorides
and carbon dioxide. Rajput and Negi (2011) from Bhimtal Lake of
Kumaon Himalaya of Uttarkhand, reported that Gross primary
productivity is positively correlated with Net primary productivity and
water transparency and negatively correlated with water temperature, air
temperature, nitrate, phosphate, chlorides, dissolved solids and chlorides
whereas Net primary productivity is positively correlated with pH and
Gross primary productivity, turbidity, total alkalinity, dissolved oxygen,
total hardness and water transparency whereas negatively correlated
with water temperature, air temperature, pH and phosphate.
COMMUNITY RESPIRATION (gC/m3/hr):
Community respiration means deducting the net primary
productivity from gross primary productivity and conververted into Co2
release.
In Mombatta Lake, minimum Community respiration was observed
in the months of August and September whereas, maximum in the
months of October and November. In Kagzipura Lake, minimum
Community respiration was observed in the months of July and August
whereas, maximum in the months of April and May. Average seasonal
record of Community respiration in Mombatta Lake showed that,
minimum in monsoon season and maximum in winter season. Average
seasonal record of Community respiration in Kagzipura Lake showed
Page 83
that, it is found minimum in rainy season and maximum in summer
season.
Community respiration is high during the summer season and low
during the monsoon season. (Majagi and Vijaykumar, 2005).
Chattoppadhyay and Banerjee (2008) from Krishnasayar Lake at
Burdwan reported that Community respiration is maximum in the
month of April and minimum in September. Bhosle et al (2010) from
some selected lake of three districts, Maharashtra.
Shallow Lake water leads to a rapid change in the productivity with
the change in Physico-chemical conditions of water. Due to high
respiration of all living organisms and non living organic matter reduce
the dissolved oxygen content (Leonard et al, 2000). This observation
supports the present study as values of dissolved oxygen content were
found lower during the summer season in Mombatta and Kagzipura
Lake.
According to Radwan (2005) rate of respiration attained highest
values in summer months was due to the effect of drainage water
discharged from the different drains around the station. These effluents
enhance the biological activities of bacteria, especially in summer
months due to the decomposition of organic matter. Similar findings are
observed in present study for Kagzipura Lake because Kagzipura Lake
receives domestic sewage from surrounding village and other human
activities responsible for maximum community respiration. And also low
count of phytoplankton and high density of zooplanktons might be
responsible for high values of community respiration. Similar findings
are reported by Sheriff and Ezz (1988) from Burulus Lake of Egypt.
Radwan (2005) reported maximum primary productivity for Lake
Page 84
Burulus of Egypt in summer season and minimum in winter and
monsoon season. Such findings are supported the present study. Values
of community respirations of Kagzipura Lake are higher than the
Mombatta Lake.
Patil and Chavan (2010) for three lakes of Sangli district and
Sawant et al (2010) for Atyal Pond in Gadhinglaj Tahsil, Dist. Kolhapur,
reported that community respiration is increased during summer and
decreased in monsoon season.
Statistical analysis of data collected for Mombatta Lake revealed
that community respiration is positively correlated with Gross primary
productivity whereas, negatively correlated with Net production efficiency
and no correlation with Net primary productivity and Respiration.
Statistical analysis of data collected for Kagzipura Lake revealed that
community respiration is positively correlated with respiration and
negatively correlated with Net production efficiency whereas no
correlation with Gross primary productivity and Net primary
productivity.
Majagi and Vijaykumar (2005) reported that community
respiration is positively correlated with Gross primary productivity, water
temperature, dissolved oxygen, total alkalinity, chloride, Rotifera,
Copepoda and Cladocera.
NET PRODUCTION EFFICIENCY (gC/m3/hr):
Net production efficiency is the ratios measure the efficiency with
which an organism converts assimilated energy into primary or
secondary production.
Page 85
In Mombatta Lake, minimum Net production efficiency was
observed in the months of August and September whereas, maximum in
the months of October and November. In Kagzipura Lake, minimum Net
production efficiency was observed in the months of April and May
whereas maximum Net production efficiency was recorded in the months
of August and September. Average seasonal record of Net production
efficiency in Mombatta Lake showed minimum in monsoon season and
maximum in winter season. Average seasonal record of Net production
efficiency in Kagzipura Lake showed minimum in summer season and
maximum in winter season.
Chattoppadhyay and Banerjee (2008) for Krishnasayar Lake at
Burdwan reported that Net production efficiency is maximum in
September and minimum in April. Their seasonal record shows that
maximum in monsoon and minimum in winter season. Chinnaiah and
Madhu (2010) for Darmasagar Lake in Adilabad reported that Net
production efficiency was maximum in the month of November and
minimum in the month of October. Their seasonal record shows that Net
production efficiency was maximum in monsoon and summer, and
minimum in winter season. Such findings inverse relationship to present
study of Mombatta and Kagzipura Lake , in which Net production
efficiency increased in winter and decreased monsoon and summer
season .
Statistical analysis of data collected for Mombatta Lake revealed
that net production efficiency is negatively correlated with gross primary
productivity, community respiration and respiration whereas no
correlation with net primary productivity. Statistical analysis of data
collected for Kagzipura Lake revealed that Net production efficiency
Page 86
negatively correlated with Gross primary productivity, Net primary
productivity, Community respiration and Respiration.
RESPIRATION (gC/m3/hr):
In Mombatta Lake minimum Respiration was observed in the
months of August and September whereas maximum Respiration was
recorded in the months of October and November. In Kagzipura Lake
minimum Respiration was observed in the months of March and
September whereas maximum Respiration was recorded in the months of
January and May. Average seasonal record of Respiration in Mombatta
Lake showed minimum in monsoon season and maximum in winter
season. Average seasonal record of Respiration in Kagzipura Lake
showed minimum in monsoon season and maximum in summer season.
Chinnaiah and Madhu (2010) for Darmasagar Lake in Adilabad
reported that Respiration (% of GPP) was maximum in the month of
October and minimum in February. Their Seasonal record shows that
maximum in winter and summer and minimum in monsoon seasons.
Such findings are supported to present study of Mombatta and
Kagzipura Lake.
Statistical analysis of data collected for Mombatta Lake re vealed
that net production efficiency is negatively correlated with gross primary
productivity, net primary productivity and net production efficiency, and
no correlation with community respiration. Statistical analysis of data
collected for Kagzipura Lake revealed that respiration positively
correlated with community respiration and negatively correlated with net
production efficiency whereas no correlation with gross primary
productivity and net primary productivity.
Page 87
REFERENCES
Abbasi, S. A and Chari, K. B (2008): Environmental Management of
Urban Lakes with special reference to Oussudu. Daya Publishing House Pvt.Ltd. New Delhi. Pp 82-87.
Ahmed S. H and Singh, A. K (1989): Correlation between antibiotic
factors of water and zooplanktonic communities of a tank in Patna, Bihar. In. Proc. Nat. Sem. on Forty years of Freshwater Aquaculture in
India. 7-9 November, 1989, Central Institute of Freshwater Aquaculture,
Bhubhneshwar Pp.119-121.
Andersen, J. H., Schluter, L., and Ertebjerg, G (2006): Coastal
eutrophication: recent developments in definitions and implications for
monitoring strategies. J. Plankton Res. 28 621–628.
Anjinappa, H (2002): Hydrobiological studies and Avi-fauna at Bonal reservoir, Shorapur Gulberga district, Ph.D Thesis, Gulberga, University,
Gulberga. Pp.156.
Aravind Kumar, (1997) :Comparative hydrological studies of tropical water bodies with special reference to sewage pollution in south Bihar. J.
Ecobiol., 9(4): 255-262
Arvindkumar (1995): Some limnological aspects of the freshwater tropical wetland of Santhal Paranga (Bihar), Indian J.Env and Poll. 2 (3):
137-141.
Ayyapan, S and Gupta T. R. C (1985): Limnology of Rammascrudra tank primary production. Bull.Soc.Sagx 32: 82-88.
Benton, A. H. and Werner, W. E (1972): Manual of field biology and
ecology. 5th edition. Burgess Publishing Company. Minniapolis, Minnesota.
Bhosle, L., Dhumal, S and Sable, A (2010): Seasonal variations in
occurrence of phytoplankton and primary productivity of some selected lakes in Maharashtra. The Bioscan, Vol. 2: 569-578.
Bhushan, P. B and Singh, B (2003): Ecological status in relation to
primary productivity of a tropical water body, East Champarns, Bihar, Nature Env. and Poll. Tech., 2 (4): 387-390.
Page 88
Chinnaiah, B and Madhu, V (2010): Primary productivity of
Darmasagar Lake in Adilabad, Andhra Pradesh, India. International Journal of Pharmacy and Life Sciences, 1(8): 437-439.
Cole, G. A (1983): Textbook of Limnology.3rd edition. The C.V. Mosby
Company. USA. 401 Pp.
Das, A. K (2002): Phytoplankton Primary production in some selected
reservoirs of Andhra Pradesh. Geobios.29:52-57.
Datta, N. C, Mandal N and Bandopodhya, B. K (1984): Seasonal
variations of primary productivity in relation to some physico chemical
properties of a freshwater pond, Kolkata. Int. J.Acad. Ischthyol, 5: 113-
120.
Davis, C. C., (1955): The Marine and Freshwater plankton. Constable
and Company Ltd., London, pp 539.
Dodson, S. I., Arnott, S.E and Cottingham, K. L (2000): the
relationship in lake communities between primary productivity and
species richness. Ecology 8 (10): 2662-2679.
Elser, J., Elser, M., MacKay, N and Carpenter, S (1988): Zooplankton
mediated transitions between N- and P- limited algal growth. Limnology
and Oceanography 33: 1-14.
Fee, E. J (1998): Computer Programs for calculating in situ
phytoplankton photosynthesis. Canadian Technical Report of Fisheries
and Aquatic Sciences, No. 1740.
Flanagan, K and McCauley, E (2008): Depth and warming interact to
affect carbon dioxide concentration in aquatic mesocosms. Freshwater
Biology 53: 669-680
Gaarder, T and Gran, H. H (1927): Investigation of the production of
plankton in the Oslo Fiord. Rapp. et Proc-Verb. Cons. Internat. Explor.
Scient. Mer. Mediterr. 42: 1-48.
Hujare, M. S and Muley, M. B (2007): Studies on the primary
productivity in the perennial tanks from Kolhapur district (Maharashtra),
India. Indian Journal of Environment and Ecoplaning, 14 (3): 683-690.
Joseph, K and Shanthi, K (2010): Assessment of the primary
productivity of Muvattupuzha River, Kottayam, Kerala. J.Ecotoxicol.
Environ. Monit. 20 (4) 355-358.
Page 89
Kaur, T., Arst, A., Noges, T and Tuvikene, L (2009): Estimation of the
phytoplankton productivity in three Estonian lakes. Estonian Journal of Ecology. Vol 58 (4):297-312.
Koli, V. K and Ranga, M. M (2011): Physicochemical status and
Primary productivity of Ana Sagar Lake, Ajmer (Rajasthan), India.
Kumar, H. D (1990): Introductory Phycology. Affiliated East-West Press
Pvt. Ltd. New Delhi.
Meding, M and Jackson, L (2003): Biotic, chemical and morphometric
factors contributing to winter anoxia in prairie lakes. Limnology and
Oceanography 48: 1633-1642.
Mitsch, W. J. and Gosselink, J. G (1993): Wetlands, 2nd edition. Van
Nostrand Reinhold, New York, USA, 722 Pp.
Mohan, J. P. J., Wesley, S. G., Ramya, S., Alaguchamy, N.,
Kalayanasunderam, M and Jayakumaraj, R (2010): Seasonal
variations in the phytoplankton diversity and Primary productivity of
Pechiparai reservoir, Kanyakumari. Journal of Ecobiology. Vol. 26(4):
319-323.
Mungikar, A. M (2003): An Introduction to Biometry. Saraswati
Publication, Aurangabad. Pp. 1-63.
Odum, E. P (1971): Fundamentals of ecology. 3rd edition. Philadelphia,
W.B. Saunders. Co: 574 Pp. London, Toronto.
Palahiappan, N., Marimathu, R and Rajendra, M (1981): Seasonal
variations in primary productivity of two rock pools in Salem, Tamilnadu.
Instit.Experimental.Boil. Pp 58-62.
Pandey, B. N., Jha, A.K. and Das, P.K.L. (1994): Hydrobiological study
of a swamp at Purina, Bihar in relation to phytoplankton fauna. J.
Ecobiol., 6(1): 0.13-0.16.
Pandey, J., Pandey, U and Tyagi, H. R (1999): The relation of algal productivity to the nature of physico chemical environment of a
freshwater tropical lake, Ecol. Env and Cons. Vol. 5 (4): 365-368.
Patil, A. and Chavan, N. (2010): Primary productivity studies in some freshwater reservoirs of Sangli District, Maharashtra. Nature
Environment and Pollution Technology. 9(1): 101-103.
Page 90
Patil, S and Sahu, B. K (1993): Studies on the primary production in
Rengali reservoir (Orissa). J. Ecotoxicology. 5 (2): 85-88.
Prabhakar V. M, Vaidya, S. P., Garud, V. S. and Swain K. K. (2009): “Trend of Primary Production in Khadakwasla Reservoir“, 13th World
Lake Conference, Wuhan, China.
Prakash, S (2001): Seasonal dynamics of plankton in a freshwater body
at Balarampur. Geobios. 28: 29-32.
Prasad, D. Y. (1990): Primary Productivity and Energy Flow in Upper
Lake, Bhopal. Indian J. Environ Health. 32(2): 132-139.
Radwan, A. M (2005): Some factors affecting the primary production of
phytoplankton in Lake Burrulus. Egyptian Journal of Aquatic Research.
Vol. 31(2): 72-88.
Rodhe, W (1970): Crystallization of eutrophication concepts in Northern
Europe. Eutrophication: Causes, Consequences, Correctives Washington,
DC National Academy of Sciences Pp. 50–64.
Saadaun, I., Bataineh, E and Handal, A. Y (2008): The primary
production conditions of Wadi Al-Arab Dam (reservoir), Jordon. Jordon
Journal of Biological Science. Vol 1 (2):67-72.
Sahu, B.K., Roa, R.J., Behera, S.K. and. Pundit, R.K. (1995): Phytoplankton and primary production in the River Ganga from
Rishikesh to Kanpur. J. Ecobiol., 7(3): 219-224.
Sharma, M and Sahai, Y. N (1988): Primary productivity of Jari tank.
Proc.Nat.Symp. Past, Present and Future of Bhopal Lake.Pp. 97-104.
Sharma, R (1993): Limnological studies on the Yeshwanth Sagar reservoir with special reference to plankton population dynamics. Ph.D.
thesis. Devi, Ahilya Vishwavidyalaya, Indore. (M.P).
Sharma, R. and Sharma, K.C. (1992): Diatoms of Anasagar lake of
Aimer, Rajasthan, Acta. Ecol., 14: 6-9.
Sherif, Z. M and Ezz, S. M (1988): Preliminary study on phytoplankton
zooplankton relationship in lake Burullus. Egypt. Bull.Inst.
Oceanogr.Fish. A. R. E., 14(1): 23-30.
Shukla, A. N and Pawar, S (2001): Primary productivity of Govindgarh
Lake, Rewa (M.P), India. J.Environ.Poll. 8 (3): 249-253.
Page 91
Shukla, S. N. and Bais, V. S. (1990): Changes in physico chemical
profile of the Bila reservoir during winter season. Trends in Ecotoxicology. Pp. 37-41.
Singh, F. D (1986): Relation between primary productivity and
environmental parameters of tropical lakes. Stat.Anal.Poll.Res.5 (3&4): 103-110.
Singh, R. K and Desai, V. R (1980): Limnological observations on
Rihand reservoir, part III, primary productivity. J.Inland.Fish.Soc.India.12 (2): 63-68.
Singh, V. K. and Sharma, A. P (1999): Hydrobiological characteristics
and primary production in fish pond manured with different organic manures. Indian J.Fish. 46 (1): 79-85.
Sivakumar, K and Karuppasamy, R (2008): Factors Affecting
Productivity of Phytoplankton in a Reservoir of Tamilnadu, India .American-Eurasian Journal of Botany, 1 (3): 99-103, 2008.
Smith, V. H (2007): Using primary productivity as an index of coastal
eutrophication: the units of measurement matter. Journal of Plankton Research. Vol. 29 (1): 1-6.
Sobha, V. S., Santhosh, T., Gayadevi, P and Sheeba, S (2003):
Primary productivity of Paravar canal-An analysis. Eco.Env and Cons. 9 (4): 441-444
Sukumaran, P. K and Das, A. K (2002): Distribution of phytoplankton
in some freshwater reservoirs Karnataka. J. Inland Fish Society, India. 33 (2): 29-36.
Sultan, S., Chauhan, M and Sharma, V. I (2003): Physicochemical
status and primary productivity of Pahunj reservoir, Uttar Pradesh. J.Inland Fish Soc. India, 35:73-80.
Synudeen, S. S. (2002): Primary productivity studies in some aquatic
bodies of Kollam district, Kerala. Uttar Pradesh J. Zool. 22(3): 247-250.
Tonapi, G. T (1980): Fresh Water Animals of India (An Ecological
Approach). New Delhi: Oxford & IBH. Publ.Co.341 pp.
Page 92
Usha, R., Ramalingam, K and Rajan, U.D (2006): Freshwater lakes- a
potential source for aquaculture activities- a model study on Perumal Lake, Cuddalore, Tamilnadu. Journal of Environmental Biology. Vol.
27(4):713-722.
Vasanthkumar, B and Vijaykumar, K (2011): Diurnal variation of physicochemical properties and primary productivity of phytoplankton in
Bheema River, Gulberga.Recent Research in Science and Technology,
3(4): 39-42.
Vasanthkumar, B., Vijaykumar, K., Reddy, B. R and Kalpana, M. R (1996): Effect of dairy effluents on primary production of phytoplankton
in freshwater fishpond at Gulberga, Karnataka. Proc.Acad.Environ.Biol 5
(2): 145-148.
Verma, J. P. and Mohanty, R. C.(1995): Phytoplankton of Malyanta
pond of Laxmisagar and its correlation with physicochemical parameters.
Poll Res., 14: 243-253.
Vijaykumar, K (1994): Seasonal variations in the primary productivity of
tropical pond, Gulberga. J.Ecobiology. 6 (3): 207-211.
Vijaykumar, K and Paul, R (1990): Physico chemical studies of the
Bhosghu reservoir in Gulberga Kolkata. J. Ecobiol. 2 (4): 330-335.
Vijaykumar, K., Anjinappa H., Viruppanna and Padmavati, C (2000): Seasonal variations in the primary productivity of Gobbur tank,
Gulberga. Proc.Acad. Environ.Biol. 9 (2): 119-123.
Vollenweider, R. A (1974): A manual on methods for measuring primary
production in aquatic environments. 2nd
Ed. Blackwell Scientific Publications, Oxford. 225 p.
Vollenweider, R.A (1969): a manual on methods for measuring primary
production in aquatic environments, IBP Handbook No. 12, F.A.Davis
Co., Philadelphia.`
Vollenweider, R.A., Munawar, M and Stadelmann, P (1974): A
comparative review of phytoplankton and primary production in the
Laurentian Great Lakes. J. Fish. Res. Bd. Can. 31: 739-762.
Wetzel, R. G (2001): Limnology. Lake and River Ecosystems. 3rd Ed.
Academic Press, San Diego. Xvi, 1006 pp.
Page 93
Wetzel, R. G and Likens, G. E (2000): Limnological Analyses. 3rd Ed.
Springer, New York. Xv, 429 pp.
Wondie, A., Mengistu, S., Vijverberg, J and Dejen (2007): Seasonal
variation in primary production of a large high altitude tropical lake
(Lake Tana, Ethiopia): effects of nutrient availability and water transparency, Auat. Ecol, Vol. 41, Pp 195-207.
Yeragi S. G., Babu K. N and Yeragi S. S. (2002): Estimation of gross
primary production of urban creek. Proc.The National Seminar on Creeks, Estuaries and Mangroves, Thane. Poll and Cons. Pp.93-
TABLE 1: Monthly record of Primary Productivity of freshwater Mombatta Lake during
October 2008 to September 2009.
Parameter →
Months ↓ GPP
(gC/m3/hr) NPP
(gC/m3/hr) CR
(gC/m3/hr) NPE
(%)
RESP
(% of GPP)
October 2008 1.72 ± 0.31 1.66 ± 0.12 0.06 ± 0.19 96.51 ± 0.32 3.48 ± 0.028
November 1.64 ± 0.38 1.56 ± 0.12 0.08 ± 0.16 95.12 ± 0.25 4.87 ± 0.037
December 1.36 ± 0.35 1.32 ± 0.23 0.04 ± 0.11 97.05 ± 0.27 2.94 ± 0.014
January 2009 1.42 ± 0.59 1.36 ± 0.18 0.06 ± 0.10 95.77 ± 0.41 4.22 ± 0.032
February 1.46 ± 0.41 1.35 ± 0.27 0.11 ± 0.14 92.46 ± 0.14 7.53 ± 0.16
March 1.53 ± 0.54 1.30 ± 0.26 0.23 ± 0.23 84.96 ± 0.36 15.03 ± 1.41
April 1.82 ± 0.33 1.62 ± 0.29 0.20 ± 0.12 89.01 ± 0.12 10.98 ± 0.70
May 1.87 ± 0.21 1.68 ± 0.41 0.19 ± 0.24 89.83 ± 0.35 10.16 ± 0.64
June 0.94 ± 0.17 0.82 ± 0.21 0.12 ± 0.16 87.23 ± 0.27 12.76 ± 0.82
July 0.62 ± 0.30 0.54 ± 0.19 0.08 ± 0.16 87.09 ± 0.14 12.90 ± 0.86
August 0.58 ± 0.30 0.51 ± 0.48 0.07 ± 0.18 87.93 ± 0.27 12.06 ± 0.78
September 0.55 ± 0.29 0.52 ± 0.18 0.03 ± 0.11 94.54 ± 0.35 5.45 ± 0.70
Values are in an average of 8 samples ± Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 2: Monthly record of Primary Productivity of freshwater Mombatta Lake during
October 2009 to September 2010.
Parameter →
Months ↓ GPP
(gC/m3/hr) NPP
(gC/m3/hr) CR
(gC/m3/hr) NPE
(%)
RESP
(% of GPP)
October 2009 1.76 ± 0.17 1.68 ± 0.12 0.08 ± 0.01 95.45 ± 0.24 4.54 ± 0.039
November 1.67 ± 0.24 1.59 ± 0.15 0.08 ±0.02 95.20 ± 0.14 4.79 ± 0.042
December 1.28 ± 0.29 1.21 ± 0.24 0.07 ±0.04 94.53 ± 0.34 5.46 ± 0.064
January 2010 1.39 ± 0.23 1.30 ± 0.13 0.09 ±0.16 93.52 ± 0.36 6.47 ± 0.14
February 1.46 ± 0.38 1.34 ± 0.22 0.08 ±0.06 91.78 ± 0.27 5.47 ± 0.062
March 1.58 ± 0.29 1.32 ± 0.14 0.26 ±0.03 83.54 ± 0.25 16.45 ± 1.72
April 1.64 ± 0.39 1.44 ± 0.29 0.20 ±0.10 87.80 ± 0.28 12.19 ± 1.10
May 1.78 ± 0.21 1.47 ± 0.10 0.31 ±0.08 82.58 ± 0.36 17.41 ± 1.84
June 0.88 ± 0.28 0.84 ± 0.22 0.04 ±0.06 95.45 ± 0.23 4.54 ± 0.069
July 0.64 ± 0.34 0.58 ± 0.17 0.06 ±0.12 90.62 ± 0.28 9.37 ± 0.42
August 0.54 ± 0.14 0.50 ± 0.18 0.04 ±0.12 92.59 ± 0.22 7.40 ± 0.50
September 0.51 ± 0.13 0.48 ± 0.23 0.03 ±0.09 94.11 ± 0.35 5.88 ± 0.027
Values are in an average of 8 samples ± Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 3: Average of monthly record of Primary Productivity of Freshwater Mombatta Lake
during October 2008 to September 2010.
Parameter →
Months ↓
GPP
(gC/m3/hr)
NPP
(gC/m3/hr)
CR
(gC/m3/hr)
NPE
(%)
RESP
(% of GPP)
October 1.74 ± 0.03 1.67 ± 0.01 0.07 ± 0.01 95.98 ± 0.31 0.75 ± 0.035
November 1.65 ± 0.02 1.58 ± 0.02 0.08 ± 0.01 95.16 ± 0.23 0.06 ± 0.007
December 1.32 ± 0.06 1.27 ± 0.08 0.06 ± 0.02 95.79 ± 0.25 1.78 ± 0.049
January 1.40 ± 0.02 1.33 ± 0.04 0.08 ± 0.02 94.65 ± 0.32 1.59 ± 0.035
February 1.47 ± 0.02 1.35 ± 0.01 0.10 ± 0.02 92.12 ± 0.32 0.48 ± 0.012
March 1.55 ± 0.04 1.31 ± 0.01 0.25 ± 0.02 84.25 ± 0.18 1.00 ± 0.014
April 1.73 ± 0.13 1.53 ± 0.13 0.20 ± 0.01 88.41 ± 0.22 0.86 ± 0.049
May 1.82 ± 0.06 1.58 ± 0.15 0.25 ± 0.08 86.21 ± 0.14 5.13 ± 0.94
June 0.91 ± 0.04 0.83 ± 0.01 0.08 ± 0.06 91.34 ± 0.28 5.81 ± 0.98
July 0.63 ± 0.01 0.56 ± 0.03 0.07 ± 0.01 88.86 ± 0.16 2.50 ± 0.14
August 0.56 ± 0.03 0.51 ± 0.01 0.06 ± 0.02 90.26 ± 0.15 3.30 ± 0.26
September 0.53 ± 0.03 0.50 ± 0.03 0.03 ± 0.01 94.33 ± 0.20 0.30 ± 0.014
±Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 4 Seasonal record of Primary Productivity of Mombatta Lake during October
2008 to September 2009 and October 2009 to September 2010.
Seasons→
Parameters↓
2008-2009 2009-2010
Winter Summer Monsoon Summer Winter Monsoon
GPP
(gC/m3/hr) 1.54 ± 0.17 1.67 ± 0.21 0.67 ± 0.18 1.53 ± 0.23 1.62 ± 0.13 0.64 ± 0.17
NPP
(gC/m3/hr) 1.48 ± 0.16 1.49 ± 0.19 0.60 ± 0.15 1.45 ± 0.23 1.39 ± 0.07 0.6 ± 0.17
CR
(gC/m3/hr) 0.06 ± 0.02 0.19 ± 0.05 0.08 ± 0.04 0.08 ± 0.01 0.21 ± 0.10 0.043 ± 0.01
NPE
(%) 96.11 ± 0.84 89.07 ± 3.11 89.20 ± 3.58 94.68± 0.86 86.43 ± 4.23 93.19 ± 2.08
RESP.
(% of GPP) 3.88 ± 0.84 10.93 ± 3.11 10.79 ± 3.58 5.32 ± 0.86 12.88 ± 5.44 6.79 ± 2.08
± Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 5: Average of seasonal record of primary productivity of Mombatta Lake during
October 2008 to September 2010.
Seasons→
Parameters↓ Winter Summer Monsoon
GPP(gC/m3/hr) 1.53 ± 0.19 1.65 ± 0.15 0.66 ± 0.17
NPP(gC/m3/hr) 1.46 ± 0.19 1.44 ± 0.13 0.60 ± 0.15
CR (gC/m3/hr) 0.07 ± 0.010 0.20 ± 0.07 0.06 ± 0.02
NPE (%) 95.39 ± 0.60 87.74 ± 3.37 91.19 ± 2.32
RESP.(% of GPP) 1.04 ± 0.79 1.86 ± 2.18 2.97 ± 2.27
± Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 6: Simple correlation coefficient (r) of Primary Productivity of Mombatta Lake
during October 2008 to September 2010.
PARAMETERS GPP NPP CR NPE RESP
GPP 0.000
NPP 0.991** 0.000
CR 0.609* 0.498 0.000
NPE -0.075 0.056 -0.814** 0.000
RESP -0.210 -0.530 0.175 -0.369 0.000
** = significant at 1% (p < 0.01); *=significant at 5% (p<0.05)
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 7: Monthly record of Primary Productivity of freshwater Lake of Kagzipura
during October 2008 to September 2009.
Parameter →
Months ↓
GPP
(gC/m3/hr)
NPP
(gC/m3/hr)
CR
(gC/m3/hr)
NPE
(%)
RESP
(% of GPP)
October 2008 3.32 ± 0.27 3.14 ± 0.36 0.18 ± 0.07 94.57 ± 0.25 5.42±0.027
November 3.26 ± 0.17 3.10 ± 0.22 0.16 ± 0.05 95.09 ± 0.24 4.90±0.035
December 1.62 ± 0.15 1.54 ± 0.25 0.08 ± 0.07 95.06 ± 0.30 4.93±0.049
January 2009 1.82 ± 0.22 1.71 ± 0.18 0.11 ± 0.11 98.95 ± 0.34 6.04±0.12
February 1.90 ± 0.21 1.83 ± 0.13 0.07 ± 0.21 96.31 ± 0.39 3.68±0.014
March 2.07 ± 0.17 1.85 ± 0.14 0.23 ± 0.12 89.37 ± 0.28 11.11±0.84
April 2.18 ± 0.19 1.87 ± 0.10 0.31 ± 0.09 85.77 ± 0.24 14.22±1.14
May 2.29 ± 0.13 2.10 ± 0.16 0.19 ± 0.07 91.70 ± 0.27 8.29±0.49
June 1.46 ± 0.13 1.36 ± 0.24 0.10 ± 0.09 93.15 ± 0.25 6.48±0.10
July 1.14 ± 0.27 1.07 ± 0.17 0.07 ± 0.07 93.85 ± 0.35 6.14±0.21
August 1.09 ± 0.29 1.05 ± 0.12 0.04 ± 0.08 96.33 ± 0.32 3.66±0.029
September 1.02 ± 0.16 0.99 ± 0.12 0.03 ± 0.04 97.05 ± 0.39 2.94±0.014
Values are in an average of 8 samples ± Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 8: Monthly records of Primary Productivity of freshwater Lake of Kagzipura during
October 2009 to September 2010.
Parameter →
Months ↓
GPP
(gC/m3/hr)
NPP
(gC/m3/hr)
CR
(gC/m3/hr)
NPE
(%)
RESP
(% of GPP)
October 2009 3.28 ± 0.12 3.16 ± 0.28 0.12 ± 0.12 96.34 ± 0.29 3.65 ± 0.035
November 3.22 ± 0.12 3.14 ± 0.29 0.08 ± 0.21 97.51 ± 0.22 2.48 ± 0.014
December 1.58 ± 0.27 1.51 ± 0.19 0.07 ± 0.13 95.56 ± 0.32 4.43 ± 0.049
January 2010 1.88 ± 0.01 1.73 ± 0.13 0.15 ± 0.10 92.02 ± 0.38 7.97 ± 0.27
February 1.94 ± 0.14 1.86 ± 0.19 0.08 ± 0.14 95.87 ± 0.39 4.12 ± 0.078
March 2.12 ± 0.22 1.89 ± 0.14 0.23 ± 0.27 89.15 ± 0.31 10.84 ± 0.35
April 2.22 ± 0.13 1.82 ± 0.18 0.30 ± 0.15 81.98 ± 0.35 13.51 ± 0.92
May 2.32 ± 0.23 1.93 ± 0.23 0.39 ± 0.17 83.18 ± 0.28 16.81 ± 1.27
June 1.52 ± 0.39 1.38 ± 0.20 0.14 ± 0.19 90.78 ± 0.24 9.21 ± 0.84
July 1.12 ± 0.19 1.05 ± 0.21 0.07 ± 0.27 93.75 ± 0.29 6.25 ± 0.14
August 1.10 ± 0.28 1.07 ± 0.19 0.03 ± 0.18 97.27 ± 0.26 2.72 ± 0.022
September 1.06 ± 0.17 1.02 ± 0.24 0.04 ± 0.12 96.22 ± 0.32 3.77 ± 0.049
Values are in an average of 8 samples ± Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 9 Average of monthly record of Primary Productivity of Freshwater Kagzipura
Lake during October 2008 to September 2010.
Parameter →
Months ↓
GPP
(gC/m3/hr)
NPP
(gC/m3/hr)
CR
(gC/m3/hr)
NPE
(%)
RESP
(% of GPP)
October 3.30 ± 0.03 3.15 ± 0.01 0.15 ± 0.04 95.46 ± 0.21 1.25 ± 0.032
November 3.24 ± 0.03 3.12 ± 0.03 0.12 ± 0.06 96.30 ± 0.27 1.71 ± 0.045
December 1.60 ± 0.03 1.53 ± 0.02 0.08 ± 0.01 95.31 ± 0.32 0.35 ± 0.017
January 1.85 ± 0.04 1.72 ± 0.01 0.13 ± 0.03 95.49 ± 0.25 4.90 ± 0.82
February 1.92 ± 0.03 1.85 ± 0.02 0.08 ± 0.01 96.09 ± 0.36 0.31 ± 0.014
March 2.10 ± 0.04 1.87 ± 0.03 0.23 ± 0.01 89.26 ± 0.22 0.16 ± 0.010
April 2.20 ± 0.03 1.85 ± 0.04 0.31 ± 0.01 83.88 ± 0.23 2.68 ± 0.052
May 2.31 ± 0.02 2.02 ± 0.12 0.29 ± 0.14 87.44 ± 0.18 6.02 ± 0.92
June 1.49 ± 0.04 1.37 ± 0.01 0.12 ± 0.03 91.97 ± 0.19 1.68 ± 0.035
July 1.13 ± 0.01 1.06 ± 0.01 0.07 ± 0.01 93.80 ± 0.24 0.07 ± 0.003
August 1.10 ± 0.01 1.06 ± 0.01 0.04 ± 0.01 96.80 ± 0.14 0.66 ± 0.035
September 1.04 ± 0.03 1.01 ± 0.02 0.04 ± 0.01 96.64 ± 0.32 0.59 ± 0.029
± Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 10 Seasonal records of primary productivity of Kagzipura Lake during October
2008 to September 2009 and October 2009 to September 2010.
Seasons→
Parameters↓
2008-2009 2009-2010
Winter Summer Monsoon Summer Winter Monsoon
GPP
(gC/m3/hr) 2.51 ± 0.91 2.11 ± 0.17 1.18 ± 0.19 2.49 ±0.89 2.15 ± 0.16 1.20 ± 0.21
NPP
(gC/m3/hr) 2.37 ± 0.87 1.91 ± 0.13 1.12 ± 0.17 2.68 ± 0.82 1.88 ± 0.05 1.13 ± 0.17
CR
(gC/m3/hr) 0.13 ± 0.05 0.20 ± 0.10 0.06 ± 0.03 0.11 ± 0.04 0.25 ± 0.13 0.07 ± 0.05
NPE
(%) 95.92 ± 2.04 90.79 ± 4.42 95.10 ± 1.89 95.36 ± 2.36 87.55 ± 6.37 94.51 ± 2.89
RESP.
(% of GPP) 5.32 ± 0.53 9.33 ± 4.48 4.81 ± 1.77 4.63 ± 2.36 11.32 ± 5.39 5.49 ± 2.89
± Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 11: Average of seasonal records of primary productivity of Kagzipura Lake during
October 2008 to September 2010.
Seasons→
Parameters↓ Winter Summer Monsoon
GPP(gC/m3/hr) 2.50 ± 0.90 2.13 ± 0.72 1.19 ± 0.78
NPP(gC/m3/hr) 2.38 ± 0.88 1.89 ± 0.69 1.12 ± 0.73
CR (gC/m3/hr) 0.12 ± 0.03 0.23 ± 0.09 0.07 ± 0.09
NPE (%) 95.64 ± 0.44 89.16 ± 5.12 94.80 ± 2.33
RESP.(% of GPP) 2.05 ± 1.98 2.29 ± 2.37 0.75 ± 0.67
± Standard deviation of mean
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
TABLE 12: Simple correlation coefficient (r) of primary productivity of Kagzipura Lake
during October 2008 to September 2010.
** = significant at 1% (p < 0.01); *=significant at 5% (p<0.05)
Abbreviations: GPP = Gross Primary Productivity, NPP = Net Primary Productivity, CR =
Community Respiration, NPE = Net Production Efficiency, RESP = Respiration.
PARAMETERS GPP NPP CR NPE RESP
GPP 0.000
NPP 0.992** 0.000
CR 0.478 0.364 0.000
NPE -0.146 -0.023 -0.915** 0.000
RESP 0.274 0.024 0.581* -0.413 0.000
COMPARATIVE MONTHLY RECORD OF PRIMARY PRODUCTIVITY OF
MOMBATTA AND KAGZIPURA LAKE DURING OCT 2008 TO SEPT 2010.
GROSS PRIMARY PRODUCTIVITY
0.5
1
1.5
2
2.5
3
3.5
OCT NOV DEC JAN FEB MAR APR MAY JUN JUL AUG SEPT
MONTHS
gC/m
3 /hr
KAGZIPURA LAKE
MOMBATTA LAKE
Fig: 1 Comparative monthly record of Gross Primary Productivity of Mombatta and Kagzipura Lake during Oct 2008 to Sept 2010. The minimum GPP was observed in the
month of September whereas higher GPP was recorded in the month of October in both lakes.
NET PRIMARY PRODUCTIVITY
0
0.5
1
1.5
2
2.5
3
3.5
OCT NOV DEC JAN FEB MAR APR MAY JUN JUL AUG SEPT
MONTHS
gC/m
3 /hr
KAGZIPURA LAKE
MOMBATTA LAKE
Fig: 2 Comparative monthly record of Net Primary Productivity of Mombatta and Kagzipura Lake during Oct 2008 to Sept 2010. The minimum NPP was observed in the
month September and whereas higher NPP was recorded in the month of October and November in both lakes.
COMMUNITY RESPIRATION
0
0.05
0.1
0.15
0.2
0.25
0.3
0.35
OCT NOV DEC JAN FEB MAR APR MAY JUN JUL AUG SEPT
MONTHS
gC/m
3 /hr
KAGZIPURA LAKE
MOMBATTA LAKE
Fig: 3 Comparative monthly record of Community Respiration of Mombatta and Kagzipura Lake during Oct 2008 to Sept 2010. The minimum CR was observed in the month of September and maximum in April from Mombatta Lake whereas; in Kagzipura
Lake minimum CR was observed in the month of September and maximum in May.
NET PRODUCTION EFFICIENCY
83
85
87
89
91
93
95
97
99
OCT NOV DEC JAN FEB MAR APR MAY JUN JUL AUG SEPT
MONTHS
gC/m
3 /hr
KAGZIPURA LAKE
MOMBATTA LAKE
Fig: 4 Comparative monthly record of Net Production Efficiency of Mombatta and Kagzipura Lake during Oct 2008 to Sept 2010. The minimum NPE was observed in the
month of April in both lakes whereas maximum in January in Mombatta lake and November and august in Kagzipura lake.
RESPIRATION (% OF GPP)
0.05
2.05
4.05
6.05
8.05
10.05
12.05
14.05
OCT NOV DEC JAN FEB MAR APR MAY JUN JUL AUG SEPT
MONTHS
gC/m
3 /hr
KAGZIPURA LAKE
MOMBATTA LAKE
Fig: 5 Comparative monthly record of Respiration of Mombatta and Kagzipura Lake during Oct 2008 to Sept 2010. The minimum Respiration was observed in the month of September and maximum in April whereas in Kagzipura lake, minimum in the month of
November and august and maximum in the may.
COMPARATIVE SEASONAL RECORD OF PRIMARY PRODUCTIVITY OF
MOMBATTA AND KAGZIPURA LAKE DURING OCT 2008 TO SEPT 2010.
GROSS PRIMARY PRODUCTIVITY
0
0.5
1
1.5
2
2.5
3
WINTER SUMMER MONSOON
SEASONS
gC/m
3 /hr
MOMBATTA LAKE
KAGZIPURA LAKE
Fig 6: Comparative seasonal record of Gross primary productivity of Mombatta and Kagzipura Lake during Oct 2008 to Sept 2010. The minimum GPP was observed in mansoon season in both lakes whereas maximum in winter from Mombatta lake and
winter season in case of Kagzipura Lake. Average seasonal values of GPP of Kagzipura Lake higher in summer season and lower values are in monsoon season from Mombatta
Lake.
NET PRIMARY PRODUCTIVITY
0.5
0.7
0.9
1.1
1.3
1.5
1.7
1.9
2.1
2.3
2.5
WINTER SUMMER MONSOON
SEASONS
gC/m
3/hr
MOMBATTA LAKE
KAGZIPURA LAKE
Fig 7: Comparative seasonal record of Net primary productivity of Mombatta and Kagzipura Lake during Oct 2008 to Sept 2010. The minimum NPP was observed in mansoon season whereas maximum in winter season in both lakes. Average seasonal
values of NPP of Kagzipura Lake are higher in winter season and lower values in monsoon in Mombatta Lake.
COMMUNITY RESPIRATION
0.05
0.07
0.09
0.11
0.13
0.15
0.17
0.19
0.21
0.23
0.25
WINTER SUMMER MONSOON
SEASONS
gC/m
3/hr
MOMBATTA LAKE
KAGZIPURA LAKE
Fig 8: Comparative seasonal record of Community Respiration of Mombatta and
Kagzipura Lake during Oct 2008 to Sept 2010. The minimum CR was observed in winter and mansoon season whereas higher CR was recorded in summer season. Average
seasonal values of CR of Kagzipura Lake are higher in summer season and lower values in monsoon season from Mombatta Lake.
NET PRODUCTION EFFICIENCY
82
84
86
88
90
92
94
96
98
WINTER SUMMER MONSOON
SEASONS
gC/m
3/hr
MOMBATTA LAKE
KAGZIPURA LAKE
Fig 9 Comparative seasonal record of Net Production Efficiency of Mombatta and Kagzipura Lake during Oct 2008 to Sept 2010. The NPE minimum was observed in
summer season whereas higher NPE were recorded in winter and mansoon season. Average seasonal values of NPE of Kagzipura Lake are higher in winter season and lower values in summer season from Mombatta Lake.
RESPIRATION (% OF GPP)
0.7
1.2
1.7
2.2
2.7
WINTER SUMMER MONSOON
SEASONS
gC/m
3 /hr
MOMBATTA LAKE
KAGZIPURA LAKE
Fig 10: Comparative seasonal record of Respiration of Mombatta and Kagzipura Lake
during Oct 2008 to Sept 2010. In Mombatta Lake minimum Respiration was observed in winter season and maximum in monsoon season whereas in Kagzipura Lake, minimum in
monsoon season and maximum in winter season. Average seasonal values of Mombatta Lake are higher in monsoon season and lower values in winter season from Kagzipura Lake.