IJLSSR,VOLUME 3, ISSUE 1, JANUARY 2017 : 771-778

    
Research Article (Open Access)

Zooplankton Diversity in Madduvalasa Reservoir, India

Ramachandra Rao R1, Manjulatha C2*, Raju D V S N3
1Ph. D Scholar, Department of Zoology, Andhra University, Visakhapatnam, India
2Professor, Department of Zoology, Andhra University, Visakhapatnam, India
3Ph. D Scholar, Department of Zoology, Andhra University, Visakhapatnam, India

*Address for Correspondence: Dr. C. Manjulatha, Professor, Department of Zoology, Andhra University, Visakhapatnam, India
Received: 29 October 2016/Revised: 18 November 2016/Accepted: 23 December 2016

ABSTRACT- The zooplankton diversity was studied in four stations at Madduvalasa reservoir during June 2014 to May ’15 and forty five species were identified. Among eight groups, the diversity of Rotifera comprises of 17 species (21.37%), Cladocera 8 (16.44%), Copepoda 5 (17.28%), Ostracoda 2 (15.21 %), Protozoa 3 (12.24%), Crustacea 9 (11.26%), Mollusca 1 species (01.60%) respectively along with fish larvae and eggs (04.61%). The monthly and group wise zooplankton density analysed and found that the number was highest during summer followed by monsoon and lowest during winter.
Key-Words- Zooplankton, Monthly variation, Madduvalasa reservoir, Rotifera, Copepoda

INTRODUCTION- Plankton is one of the most favourable food items for many aquatic organisms; almost all the fishes at their larval stages depend on it and some of them exclusively feed on zooplankton. They invariably form an integral component for fresh water communities and contribute to biological productivity [1]. In the last two decades, much attention has been paid in tropical countries towards the study of biology, ecology and toxicology of zooplankton due to their important role in rapidly emerging concepts in environmental management like Environmental Impact Assessment (EIA). Zooplankton is good indicator of the changes in water quality because they are strongly affected by environmental conditions and respond quickly. The study of zooplankton is necessary to evaluate the fresh water reservoir in respect to their ecological and fishery status [2]. The Zooplankton community fluctuates according to physicochemical parameters of the environment, especially Rotifer species change with biotic factors [3]. Zooplankton is the link between phytoplankton and fish; hence, their qualitative and quantitative studies are of great importance.

MATERIALS AND METHODS-
Study Area: Sri Gorle Sriramulu Naidu Madduvalasa reservoir is present at Madduvalasa village of Srikakulam district, Andhra Pradesh, India (Fig. 1). Samples were collected from four stations of the above reservoir i.e., S1: Narendra puram, S2: Vangara, S3: Kottisa and S4: Gudivada agraharam.


Fig. 1. Madduvalasa reservoir (18° 35' 30''N Latitude and 83° 37' 20'' E longitude)

Collection of sample, preservation and identification: Zooplankton samples were collected randomly with plankton net (bolting silk mesh size 25µ) on monthly basis from June 2014 to May 15, between 9.00 to 10.00 am. 100 lit of surface water was sieved through the plankton net and transferred to plastic containers and 4% formalin was added for preservation; density [4] and diversity of zooplankton was studied by Lackey’s drop count method under light microscope. The total number of zooplankton present in a litre of water sample calculated by using following formula:

N = n × v / V

Where,
N = Total no. of organisms/ lit of water filtered,
n = Number of organisms counted in 1 ml of sample,
v = Volume of concentrate plankton sample (ml),
V= Volume of total water filtered through (L)

The systematic identification of plankton was made by using standard keys of various authors [5-10].

Biodiversity: The statistical calculation on biodiversity of zooplankton was studied using the formula of Shannon- Wiener diversity index and Menhinick’s index [11-12] which was calculated as follows:

1: Shannon - Wiener diversity index
Shannon-Wiener index denoted by
H = -SUM [(pi) × ln(pi)]
SUM = summation
pi = proportion of total sample represented by species i Divide no. of individuals of species i by total number of samples
S = number of species = species richness
Hmax = ln(S) Maximum diversity possible
E = Evenness = H/Hmax

2: Menhinick’s index
Menhinick’s index (d1) = S / /ÖN Where,
d1 = Menhinick’s index
S = total number of species.
ÖN = total number of organism (density)

RESULTS-
In the present study, diversity and monthly availability of zooplankton in Madduvalasa reservoir are analyzed and given in Table 1. Forty five species were identified in four stations, which consist of rotifera, cladocera, copepoda, ostracoda, protozoa, crustacea, mollusca along with fish larvae and fish eggs.

Table 1. Check list of Zooplankton species at Madduvalasa reservoir, Srikakulam dt.
Group Family Species
Rotifera Brachionidae Brachionus angularis (Gosse,1851)
Brachionus calyciflorus (Pallas, 1766)
Brachionus caudatus (Haner, 1937)
Brachionus diersicornis (Daday, 1883)
Brachionus plicatelis
Brachionus quadridentata (Hermann, 1783)
Keratella cochlearis (Gosse,1851)
Keratella tropica (Apstein, 1907)
Lecanidae Lecane lunaris (Ehrenberg,1982)
Lacane monostyla (Daday, 1897)
Gastropodidae Gastropus minor (Rousselet 1892)
Asplanchnidae Ascomorpha ovalis (Begendal, 1892)
Asplanchna sp
Synchaetidae Synchaeta sp
Polyarthra vulgaris (Carlin, 1943)
Philodinidae Philodina citrine (Ehrenberg)
Testudinellidae Filinia longiseta (Ehrenberg)
Cladocera Daphnidae Daphania pulex
Daphania carinata
Monia micrua (Kurz)
Monia brachiata
Bosminidae Bosmina longirostris
Chydoridae Alona pulchella (King)
Alona intermedia (Sars)
Alonella. Sp
Copepoda Diaptomidae Cyclopoid copepodite
Diaptomus pallidus
Cyclopidae Cyclops sp
Mesocyclops sp
Nauplius larva
Ostracoda Cyprididae Cypris sp
Stenocypris sp
Protozoa Parameciidae Paramecium caudatum
Vorticellidae Vorticella campanula
Epistylis sp
Crustacea Prawn nauplius larva
Zoea larva
Chironimid larva
Dragonfly nymph
Mayfly nymph
Damselfly nymph
Stonefly nymph
Waterbeetle nymph
Mosquito larva
Mollusca Velligar larva
Fish larvae Fish larva
Fish eggs Fish eggs

The monthly variation of zooplankton density (nos/ lit) at four stations found that the maximum number of rotifera (262 nos/lit) recorded at station 1 during May 2015 and minimum (142 nos/lit) at station 3 in November 2014. Followed by the maximum number of cladocera (186 nos /lit) recorded at station 1 occurred during May 2015 and the minimum (112 nos /lit) at station 2 in January 2015. The maximum number of copepoda (224 nos /lit) recorded at station 1 during May 2015 and minimum (120 nos/lit) at station 2 in December 2014. The maximum number of ostracoda (162 nos /lit) recorded at station1 during May 2015 and minimum (104 nos /lit) at station 4 in January 2015. The maximum number of protozoa (142 nos /lit) recorded at station 1 during May 2015 and minimum (75 nos /lit) at station 2 in January 2015. The maximum number of crustacea (132 nos /lit) recorded at station 2 during August 2014 and minimum (54 nos /lit) at station 4 in January 2015. The maximum number of mollusca (36 nos /lit) recorded at station 3 during August 2014 and the nil at summer season and the maximum number of fish larvae (66 nos /lit) recorded at station 2 during August 2014 and the number was minimum (18 nos /lit) at station 3 in May 2015 (Table 2).

Table 2. Monthly variation of zooplankton density (no. / lit) during June 2014 – May 2015
STATIONS/ MONTHS ROTIFERA CLADOCERA COPEPODA OSTRACODA
S1 S2 S3 S4 S1 S2 S3 S4 S1 S2 S3 S4 S1 S2 S3 S4
JUN-14 236 204 222 216 162 152 158 148 158 145 152 155 158 142 148 142
JUL 215 195 201 198 145 142 136 146 158 133 128 142 148 138 144 143
AUG 195 181 187 196 136 128 138 122 146 138 135 138 136 132 138 136
SEP 172 169 159 178 125 118 127 116 143 142 138 142 132 128 132 138
OCT 163 172 168 158 122 115 120 122 128 126 132 124 128 125 126 128
NOV 150 146 142 148 132 130 125 134 138 134 128 134 122 112 126 125
DEC 178 153 163 169 144 125 132 138 124 120 134 128 112 108 115 118
JAN-15 186 168 176 174 138 112 124 128 142 135 132 141 118 121 108 104
FEB 180 175 177 168 152 145 149 149 167 152 145 158 125 135 118 115
MAR 197 177 181 178 164 158 168 156 184 164 155 174 142 142 130 125
APR 205 196 188 204 178 166 172 175 202 187 164 192 158 158 142 136
MAY 262 244 254 237 186 175 178 184 224 198 188 198 162 156 155 146
TOTAL 2339 2180 2218 2224 1784 1666 1727 1718 1914 1774 1731 1826 1641 1597 1582 1556
MEAN 2240.25 1723.75 1811.25 1594.00
STATIONS/ MONTHS PROTOZOA CRUSTACEA MOLLUSCA FISH LARVAE
S1 S2 S3 S4 S1 S2 S3 S4 S1 S2 S3 S4 S1 S2 S3 S4
JUN-14 126 115 122 118 077 122 092 078 022 032 026 028 058 062 048 055
JUL 131 112 125 124 122 126 115 098 032 025 032 028 042 057 045 064
AUG 118 106 105 108 124 132 124 112 025 033 036 024 064 066 038 068
SEP 102 108 100 115 122 128 118 121 028 034 025 022 052 060 046 052
OCT 090 092 085 102 105 122 122 104 025 022 024 022 048 056 033 047
NOV 082 085 092 096 102 113 108 096 012 016 021 019 042 056 032 042
DEC 095 098 086 091 102 108 110 086 0 009 014 017 038 053 025 035
JAN-15 096 075 084 085 096 106 094 054 0 0 009 010 033 042 028 038
FEB 106 082 102 102 085 112 094 076 0 0 0 0 028 035 026 027
MAR 112 096 113 122 075 095 085 078 0 0 0 0 025 038 022 025
APR 135 102 126 131 062 077 082 065 0 0 0 0 022 032 021 019
MAY 142 118 135 138 065 082 077 072 0 0 0 0 022 027 018 022
TOTAL 1335 1189 1275 1332 1137 1323 1221 1040 144 171 187 170 474 584 382 494
MEAN 1282.75 1180.25 168.00 483.50
S1: Narendra puram, S2: Vangara, S3: Kottisa, S4: Gudivada Agraharam

The monthly group wise zooplankton diversity observed from June 2014 to May 15 at four stations (Table 3 & Fig. 2). Rotifera group in the present study observed to show a numeric superiority over other groups of zooplankton and occupied with 21.37%. Followed by copepod groups with 17.28%, cladocera with 16.44%, ostracoda with 15.21%, protozoa with 12.24%, crustacea with 11.26%, fish larvae and eggs with 4.61% and mollusca with 1.60%.

Table 3: Group wise zooplankton diversity during June 2014 – May 2015
S. No Groups Number of organisms Percentage (%)
1 Rotifera 2240.25 21.37
2 Cladocera 1723.75 16.44
3 Copepoda 1811.25 17.28
4 Ostracoda 1594.00 15.21
5 Protozoa 1282.75 12.24
6 Crustacea 1180.25 11.26
7 Mollusca 168.00 01.60
8 Fish larvae 483.50 04.61



Fig. 2

The group wise diversity in the distribution of macro and micro zooplankton was represented in Table 4 and Fig. 3. Rotifera, cladocera and copepoda were found in maximum number during summer, followed by monsoon and minimum during winter. In case of crustacea, mollusca, fish larvae and fish eggs maximum number was recorded during monsoon, followed by winter and minimum in summer. In the total population the maximum number of rotifera is 805.75 and comprises 35.97%, followed by the second largest number of copepoda is 713.00 and comprises 39.37%, cladocera is 663.75 and comprises 38.51%, ostracoda is 561.25 and comprises 35.21%, protozoa is 465.5 and comprises 36.29% during summer season. The maximum number of crustacea is 452.75 and comprises 38.36%, followed by the second largest number of mollusca is 113.00 and comprises 67.26% and fish larvae and fish eggs the number was recorded is 215.25 and comprises 45.35% during monsoon period.

Table 4. Monthly diversity of zooplankton during June 2014 to May 2015
GROUP SEASONS
MONSOON % WINTER % SUMMER %
ROTIFERA 781.00 34.86 653.50 29.17 805.75 35.97
CLADOCERA 549.75 31.89 510.25 29.60 663.75 38.51
COPEPODA 573.25 31.65 525.00 28.99 713.00 39.37
OSTRACODA 558.75 35.05 474.00 29.74 561.25 35.21
PROTOZOA 458.75 35.76 358.50 27.95 465.50 36.29
CRUSTACEA 452.75 38.36 407.00 34.48 320.50 27.16
MOLLUSCA 113.00 67.26 055.00 32.74 0 0
FISH LARVAE 219.25 45.35 162.00 33.51 102.25 21.15

Monsoon: Rotifera > Copepoda > Ostracoda > Cladocera > Protozoa > Crustacea > Fish larvae > Mollusca
Winter: Rotifera > Copepoda > Cladocera > Ostracoda > Crustacea > Protozoa > Fish larvae > Mollusca
Summer: Rotifera > Copepoda > Cladocera > Ostracoda > Protozoa > Crustacea > Fish larvae> Mollusca


Fig. 3

In the present investigation, the group wise seasonal diversity of zooplankton is represented as the maximum rotifera were recorded in summer season is 22.19% followed by monsoon 21.07% and winter 20.78%. The maximum copepoda were recorded in summer season is 19.63% followed by winter 16.69% and monsoon 15.47%. The maximum cladocera were recorded in summer season is 18.28% followed by winter 16.22% and monsoon 14.83%. The maximum ostracoda were recorded in summer season is 15.45% followed by monsoon 15.08% and winter 15.08%. The maximum protozoa were recorded in summer season is 12.82% followed by monsoon 12.38% and winter 11.40%. The maximum crustacea were recorded in winter season is 12.94% followed by monsoon 12.22% and winter 8.82%. The maximum mollusca were recorded in monsoon season is 3.05% followed by winter 1.75%. The maximum fish larvae and eggs were recorded in monsoon season is 5.92% followed by winter 5.15% and summer 2.82% (Table 5 & Fig. 4).

Table 5. Group wise seasonal diversity of zooplankton during June 2014 to May 2015
GROUP MONSOON % WINTER % SUMMER %
ROTIFERA 781.00 21.07 653.50 20.78 805.75 22.19
CLADOCERA 549.75 14.83 510.25 16.22 663.75 18.28
COPEPODA 573.25 15.47 525.00 16.69 713.00 19.63
OSTRACODA 558.75 15.08 474.00 15.07 561.25 15.45
PROTOZOA 458.75 12.38 358.50 11.40 465.50 12.82
CRUSTCEA 452.75 12.22 407.00 12.94 320.50 08.82
MOLLUSCA 113.00 03.05 055.00 01.75 0 0
FISH LARVAE 219.25 05.92 162.00 05.15 102.25 2.82
TOTAL 3706.50 3145.25 3632.00



Fig. 4

The total number of macro and micro zooplankton in this reservoir showed that the highest zooplankton numbers were noted during monsoon period (35.36%) followed by summer season (34.64%) and lowest during winter season (30.00%) (Fig 5).


Fig. 5

The biodiversity of zooplankton was calculated by using Shannon- Wiener diversity index represented that 1.98 in monsoon, 1.95 in winter and 1.82 in summer season at all four stations. The maximum diversity possible is represented 3.85 in monsoon, 3.81 in winter and 3.73 in summer season. The evenness noted 0.51 both in monsoon and winter, and 0.49 in summer season. The Menhinick’s index was represented as 0.772 in monsoon, 0.802 in winter and 0.697 in summer. These results represented that the diversity indices were more or less similar in all seasons in the reservoir (Table 6 and Fig. 6).

Table 6. Shannon-Wiener and Menhinick’s diversity index
Biodiversity Index Monsoon Winter Summer
H= Shannon-Wiener Index 1.98 1.95 1.82
Hmax= Maximum diversity possible 3.85 3.81 3.73
E = Evenness 0.51 0.51 0.49
Menhinick’s index 0.772 0.802 0.697



Fig. 6

DISCUSSION- Madduvalasa reservoir is used for irrigation and fisheries where plankton is important for fishes as a food source. The fish diversity in this reservoir was reported by Ramachandrarao and Mukundarao [13]. Taxonomic dominance has been reported in several water bodies [1, 14]. During the present study period the concentration of zooplankton was recorded to be minimum in November and maximum in June. This pattern is common in lakes, ponds, reservoirs and rivers [15]. Adoni [7] and George [16] also reported maximum of zooplankton population during summer. In present work, overall view reveals that the fluctuation of zooplankton diversity occurs distinctly in four study areas and normally in monsoon there is less population due to dilution factors in reservoir. Vasanth [17] recorded a total of 61 species of zooplanktion, in three ponds of Karwar district, Karnataka with rorifera being the dominant group.
In the present study, a total of 17 species of rotifer recorded from seven families on the whole, rotifera exhibited higher density in summer season. Rotifera play a vital role in the trophic tiers of fresh water impoundments and serve as living capsule of nutrition [18]. Sharma and Diwan [19] reported rotifera to form a dominant group during summer in Yeswinisagar reservoir; similar results were occurred at various fresh water bodies in India [20-24]. In the present investigation the population density of rotifera found rich in summer season (805.75 nos/lit) and less in winter season (653.50 nos/lit). A similar study was conducted on the number of rotifera which increased in summer may be due to the higher population of bacteria and organic matter of dead and decaying vegetation [7, 25-26]. According to Hutchinson [27], Brachionus species are very common in temperate and tropical waters indicating alkaline nature of water and excess growth of rotifera and reservoirs indicate the eutrophic conditions.
In the present study period, a total of 8 species of cladocera were recorded in three families. The population densities of cladocera were highest in summer season (663.75 nos/lit) followed by monsoon (549.75 nos/lit) and lowest in winter (510.25 nos/lit.). Diversity has also been reported higher in summer and lower in winter in Thigra Reservoir Gwalior [28] and in Majalgaon reservoir [24], cladocera is an order of small crustacea commonly called as “water fleas”. It has been reported that the density and biomass of cladocera was primarily determined by food supply [29]. Jhingran [30] recorded cladocera population to be most abundant in February, followed by July and Oct. in Ramgarh reservoir in Rajasthan. Sharma and Diwan [19] studied plankton dynamics of Yeshwantsagar reservoir in which the cladocera showed maximum density in June. Khare [31] observed an increasing trend in the months of winter season with peak during summer months March to June.He recorded minimum population during rainy season. Five species of copepoda from two families were recorded during the present study period. Copepoda showed higher population density in summer season (713 nos/lit) and lowest in winter (525 nos/lit). Similar results have also been reported to various seasonal fluctuation of zooplankton [24, 32-34]. In the present investigation two species of ostracoda were recorded from one family showing higher population diversity in summer season (561.25 nos/lit) and lowest in winter (474 nos/lit). Rajkumar [24] also reported 2 species of ostracoda a very low diversity and population density as compared to other groups of zooplankton. The population density was higher in summer season (851 org/lit) and less in Monsoon (637 org/lit). The similar results have also been observed various water bodies at different districts in India [35-37].
Three species of protozoa from two families were recorded during the present study. The density of population is highest during summer season (465.50 nos/lit) and lowest in winter season (358.5 nos/lit). Rajkumar [24] reported two species of protozoa and population density was higher in summer season (590.333 org/lit) and less in monsoon (379.333 org/lit). Similar observation was made by Shivashankar [38] at Bhadra reservoir, Karnatka. In the present investigation crustacea, mollusca, fish larvae and fish eggs play a vital role in the reservoir. The crustacea leads to sixth position in total number of organisms which comprises nine species like prawn nauplius larva¸ zoea larva, chironimid larva, dragonfly nymph, stonefly nymph, waterbeetle nymph, mosquito larva contain 11.26% in the total population. Importance of phytoplankton in Kalyanapulova reservoir was reported by Sasikala [39].

CONCLUSION- In the present study the seasonal variation in the diversity and distribution of zooplankton in Madduvalasa reservoir in all eight groups of zooplankton were recorded throughout the study period. The number was highest during summer and lowest during winter seasons in this reservoir. Shannon-wiener and Menhinicks biodiversity indices have been indicated that the zooplankton was evenly distributed in all seasons in Madduvalasa reservoir. It provides more information than simply the number of species present in four stations by revealing the abundance of rare and common species in different seasons.

REFERENCES
  1. Kanagasabhapati V and Rajan MK. A Preliminary survey of plankton in Irrukkangudi reservoir, Virudhnagar District, TN, India. Journal of Phytology, 2010, 2 (3): pp 63-72.
  2. Goswami, A.P., Mankodi, P.C. (2012). Study on zooplankton of freshwater reservoir Nyari- II Rajkot Dist, Gujarat, India, ISCA. J. Biol. Sci., 1(1): 30 34.
  3. Karuthapandi M, Rao DV and Xavier Innocent B. Zooplankton composition and diversity of Umdasager, Hyderabad. Int. J. Life Sci. Edu. Res. 2013; 1(1): 21 26.
  4. APHA. Standard methods for examination of water and waste water. 20th edn., American Public Health Association, Washington, D.C. ,1998.
  5. Pennak R.W. Freshwater Invertebrates of United states, 2nd Ed., John Wiley and Sons New York. 1968; pp 1-803.
  6. Krishnaswamy S. A Guide to the study of freshwater organisms.1973.
  7. Adoni AD, Joshi G, Gosh K, Chowasia SK, Vaishy AK, Yadav M and Verma HG. Work book on limnology, Prathibha Publishers, Sagar, India, 1985.
  8. Dhanapathi M.V.S S.S. Taxonomic notes on the Rotifera from India (from 1889-2000). Indian association of Aquatic Biologists’ (IAAB), Hyderabad. 2000.
  9. Altaff K. A manual of Zooplankton. Department of Zoology, the New College, Chennai. University Grants commission, New Delhi.2004.
  10. Lynne M Witty. Practical Guide to Identifying Freshwater Crustacean Zooplankton 2nd edition 2004; 1-49pp
  11. Shannon, C.E. and W. Weaver. The Mathematical Theory of Communication. University Illinois Press, Urbana. 1963; 1-117.
  12. Menhinick Edward F. A Comparison of Some Species- Individuals Diversity Indices Applied to Samples of Field Insects. Ecology. 1964; (45), 859–861.
  13. Ramachandrarao R and Mukundarao S. Checklist and economic classification of fresh water fishes of the Madduvalasa reservoir in Palakonda division, Srikakulam district, A.P. India. Int. J Fauna and Biological studies. 2015; 2(1): 25-29.
  14. Kudari VA, Kanamadi RD & Kadadevaru GG. Limnological studies of Attiveri and Bachanki reservoir of Utar Kannada district, Karnataka, India, Ecology, Environment and Conservation. 2005; 13(1): pp 1-6.
  15. Naveed, Md.S., A. Saboor and K.Altaff . Studies on the planktonic fauna of Madhavaram pond. Poll.Re. 2005; 24 (spl. issue): 199-204.
  16. George J P. “Limnological Investigations on the Plankton of Govindgarh Lake and Co-relation With Physico Chemical Factors”, Proc. Semi. Ecol. Fish Fresh Water Reservoir, 1970; pp. 37-46.
  17. Vasanth K. B. Khajure P. V. and Roopa, S.V. zooplankton and bacterial diversity in three ponds of Karwar District, Karnataka. Rec. Res. Sci. Tech. 2011; 39-48.
  18. Suresh Kumar, Altaff, R.K. and Raghunathan, M.B. New record of a Chydorid Cladoceran, pleuroxuy Aduncus jurine (1920), from Chennai, South India, with the description of the Development stages, International Journal of Aquatic Biology. 1999; 14 (1& 2), pp 7-10.
  19. Sharma Rekha and Diwan AP. Limnological studies of YeshwantSagar Reservoir Plankton population dynamics. Recent Advances in freshwater Biology, Ed. K.S. Rao, 1993; 1:199-211.
  20. Deshmukh U.S. Ecological studies of Chhatri Lake, Amravati with special reference to plankton and productivity. Ph. D. thesis Amravati University, Amravati. 2001.
  21. Akin-oriola G.A. Zooplankton association and environmental factors in Ogupa and Ona rivers, Nigeria. Rev. Biol. Trop. 2003; (2):391-398.
  22. Kadam S.U., Gaikwad J.M. and Md. Babar. Water quality and ecological studies of Masoli Reservoir in Parbhani District, Maharashtra. Ecology of Lakes and Reservoir Ed. V.B. Sakhare, Daya Publishing House, Delhi. 2006; pp 163-175.
  23. Rajashekhar M., Vijaykumar K. and Paerveen Zeba. Seasonal variations of Zooplankton community in freshwater reservoir Gulberga District, Karnataka, South India. Int. J. of Systems Biology. 2010; (1):6-11.
  24. Rajkumar T. Pawar. Zooplankton diversity and seasonal variation of Majalgaon reservoir, Maharashtra state, India. Int. J. Envi. Sci. 2016; 6:5.
  25. Segers H. A biogeographical analysis of rotifera of the genus Trichocerca Lamarck, 1801 with notes on taxonomy, Hydrobiologia. 2003; 500, pp 103-114.
  26. Majagi G. and Vijaykumar K. Ecology and abundance in Karanja reservoir. Environ. Monit. Asses. 2009; 152: 137-144.
  27. Hutchinson G. E. A treati se on Limnology, Vol. II: Limnoplancton. Wiley. New York.1967; 1015.
  28. Dushyant kumar Sharma and R.P Singh (2012), seasonal variation in zooplankton diversity in Tighra Reservoir Gwalior (M.P.) Indian Journal of Science and Research, 3(2), pp 155-161.
  29. Smitha P.G., Byrappa K. and Ramaswamy S.N. Physico chemical characteristics of water samples of bantwal Taluk, South-estern Karnataka, India, Journal of Environmental Biology. 2007; 595.
  30. Jhingran A.G. Limnology and production biology of two man-made lakes on Rajasthan (India) with management strategies for their fish yield optimization. Final Report IDA Fisheries Management in Rajasthan. Central Inland Fisheries Research Institute, Barrackpore, India: 1989; 1-63.
  31. Khare P.K. Physico-chemical characteristics in relation to Abundance of plankton of JagatSagar Pond, Chattapur, India. Advances in Limnology Edited by S.R. Mishra (Daya Publishing House), NewDelhi. 2005; pp 162-174.
  32. Somani V. and Pejavar M. Crustacean zooplankton of Lake Masunda, Thane, Maharashtra, International Journal of Aquatic Biology. 2004; l (19), pp 57-60.
  33. Mustapha M. K. Zooplankton assemblage of Oyun reservoir, Offa, Nigeria. Rev. Biol. Trop, International Journal of Tropical Biology. 2009; 57 (4), pp 1027-1047.
  34. Mahor R. K. Diversity and seasonal fluctuation of zooplankton in freshwater reservoir Tighra Gwalior (M.P.), Internet Referred Research Journal. 2011; 1(17), pp 47-48.
  35. Sukand B.N. and Patil H.S. Water quality assessment of Fort lake of Belgaum (Karnataka) with special reference to zooplankton, Journal of Environmental Biology. 2004; 25(1), 99-102.
  36. Kedar G.T., Patil G.P. and Yeole S.M. Effect of physicochemical factors on the seasonal abundance of zooplankton population in Rishi Lake. Proceedings of Taal 2007. The 12th world lake conference. 2008; pp 88-91.
  37. Patil S D, and Shirgur G A Morphology and identification characteristics of copepod species occurring in the government fish farm, Goregaon, Mumbai, Journal Eco biology, 2004; 16(1), pp 45-52.
  38. Shivashankar P and Venkataramana GV. Zooplankton diversity and their Seasonal varation in Bhadra Reservoir Karnatka, India. 2013.
  39. Sasikala T, Manjulatha C and D.V.S.N.Raju. Freshwater phytoplankton communities in Varaha reservoir, Kalyanapulova, Visakhapatnam. International journal of zoology studies. 2016, 1(5):5-7.
       
International Journal of Life-Sciences Scientific Research (IJLSSR) Open Access Policy
Authors/Contributors are responsible for originality, contents, correct references, and ethical issues.
IJLSSR publishes all articles under Creative Commons Attribution- Non-Commercial 4.0 International License (CC BY-NC).
https://creativecommons.org/licenses/by-nc/4.0/legalcode
      
How to cite this article:
Ramachandra RR, Manjulatha C, Raju D V S N: Zooplankton Diversity in Madduvalasa Reservoir, India. Int. J. Life. Sci. Scienti. Res., 2017; 3(1): 771-778. DOI:10.21276/ijlssr.2017.3.1.4
Source of Financial Support: Nil, Conflict of interest: Nil