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J. Env. Bio-Sci., 2014: Vol.

28 (2): 305-309 ISSN 0973-6913 (Print), ISSN 0976-3384 (On Line)

GUT CONTENT ANALYSIS OF THE CHANNA PUNCTATA (BLOCH) FROM RIVER BEAS,
HIMACHAL PRADESH, INDIA
Arun Koundal1 , Somu Koundal 2, Indu Sharma3 and Rani Dhanze4
Dept. Fisheries, COVAS, CSKHPKV, Palampur- 176062 (H.P.)1,2,4
Zoological Survey of India, High Altitude Regional Centre, Solan- 173212, H.P., India3
koundal.arun@gmail.com1 ;koundal.somu@gmail.com 2; induzsi@gmail.com3 ; rdhanze@ gmail.com4

Received: 25-09-2014 Accepted: 01-11-2014


The food and feeding of the Channa punctata (Bloch) was studied from different reaches of River Beas, based on the
collection of 153 fish ranging from 40-160 mm (SL). The studies of guts indicated that there was a preponderance of empty
stomachs during the breeding months of this fish. The insect was the dominant food item during all the months. Sand and semi
digested food of plant and animal origin also formed part of the stomach content. The highest value of Ga.SI was found during the
pre-breeding and post-breeding periods, while inverse relationship of feeding and breeding was noticed.

Analysis of gut content is widely used to ascertain the food was done as per standard procedures 22. The guts were
and feeding habits of fish species. Accurate description of diets preserved in 5% after taking their weight (in grams) and fullness
and feeding habits provides the basis for understanding the of the stomach was ascertained. Moreover gut microscopic
trophic interactions in aquatic food webs1. Feeding is usually examination was carried out by using light microscope
a part of the daily routine, the rate of which sometimes changes (OLYMPUS, CH20iBlMF).The sex, condition and weight (in
with the breeding activities of the fish. The nature of food grams) of gonad were also noticed for calculating Gonado-
composition of fish also reveals the possible habitats in which somatic index (G.S.I) of each fish. To record the number of
it lives frequently. C. punctata (Bloch) is well known for its stomachs containing one or more individuals of each food
hardy nature, can survive well in harsh environmental conditions category, frequency of occurrence method was used23. The
(low water levels, low dissolved oxygen, unclear-swampy water feeding intensity was assessed based method given by kow24.
regions etc.). Moreover it's capability of engulfing oxygen from The gut contents were isolated and identified as far as possible
air, good survivability and growth at higher densities, nutritive up to the genus or family level, following the point method25
and medicinal qualities and above all less chances of disease was adopted. The data were analyzed to obtain the percentage
makes it best option for culture practice2-8. Hence correct of empty stomachs, average index of fullness, percentage of
knowledge of the relationship of fish with its food organism is different categories of food items per fish and the percentage
essential for the production and exploitation of fish stocks. frequency of occurrence of different food items. Average index
Various workers have done the food feeding behaviour of this of fullness and Gastro-somatic index (Ga.S.I) were also
species9-14 and others15- 21 have undertaken same kind of studies calculated to find out the fullness of gut and monthly variations
in different species of Genus Channa in different climatic in feeding intensity of the fish while Gonado-somatic index
conditions. But no work has been reported so far from the (G.S.I) was monitored to indicate the spawning season and
Western Himalaya of Himachal Pradesh. So considering the frequency of spawning in different months. The respective
importance of this species the present study has been values of Ga.S.I and G.S.I in different months were plotted
conducted. graphically to find out the relationship of feeding and breeding.
Following standard formulae were used for calculations:
MATERIALS AND METHODS

Fish samples (N=153, 40-160 mm Standard length), were


collected from the sub-tributaries of river Beas i.e. Mole and
Neugal at different reaches of District Kangra (H.P) during the
period of February to October 2011. The collection was done
monthly by using diversified gears like hooks and lines, cast
nets and local fishing traps. The examination of gut contents
Gut Content Analysis of the Channa Punctata (Bloch) (306)

Table-1. List of various food items under different food groups

Table-2. Diet composition, based on % age of occurrence and % age of total points

Table-3. Monthly variations based on average index of fullness and average points/fish
(307) Koundal, Koundal, Sharma and Dhanze

Table-4. Monthly variation in abundance of food items during the study period

Fig. 1 a. Monthly variation in the Mean Ga.S.I values and G.S.I; Fig.1 b. Mean Ga.S.I in different sized groups of female and male.

based diet (Table-1). The data obtained from the (%)


RESULTS AND DISCUSSION occurrence and (%) total points revealed insect as the most
dominating group (Table-2). Moreover, on the basis of average
The gut contents were analyzed qualitatively as well as
index of fullness, average points per fish and (%) empty
quantitatively. The different food types recorded from the gut
stomachs, the monthly variations in the amount of food was
were categorized into 10 main food groups. The highest
analyzed and an inverse relationship between feeding and
percentage (69.33 %) of total food items consumed by this
breeding cycles was noticed (Table-3). The analysis based
fish were of animal origin, 19.04 (%) of the plant origin and
on monthly variation depicted the presence of abundant food
11.63 (%) of semi-digested material, which indicated that it is
varieties (table-4).
mainly a carnivorous fish that feeds mainly on animal based
food items such as insects, small sized fish, fish eggs, fish Monthly variations in the mean Ga.SI and GSI values of 105
larvae and hatchlings mainly. The copepods, cladocerans, female and 48 male fish, ranging from 40 to 160 mm SL is
molluscs, annelids and amphibians also contributed to animal presented in Fig.1.a displayed an inverse relationship of
feeding (Ga.SI) and breeding (GSI). It was observed that during
Gut Content Analysis of the Channa Punctata (Bloch) (308)

June-July (breeding period) the corresponding values of Ga.SI has also pointed out its carnivorous, surface feeding habits
decreased while increase in the GSI values was noticed in the and poor feeding intensity during spawning period14 and
same period. There was not much difference in average Ga.SI confirmed the present views.
values of both sexes except in range of 60-80mm (Fig. 1.b). Further, monthly variation in the abundance of food items based
However the Ga.SI values of male was significantly (p=0.5) on total number depicted insects as the most dominant food
higher than female in range of 140-160 mm. during all the months with the highest number (152) in April.
The (%) occurrence and (%) total points of diet composition The abundance of diatoms (19), green algae (18), molluscs
indicated that insect was, the most dominating group, while and small fish (17 each) was almost same, while copepods
the next preferred food items were small fish (12.43 %), diatoms (2), cladocerans (1) and amphibians (0) were found least in
and green algae (9.52 % each) respectively. Studies indicated number during the month of February. C. punctata (Bloch) is a
the food and feeding habits of juvenile as well as the adult C. carnivorous fish which mainly feeds upon animal based food
punctata (Bloch) and reported crustaceans, insects, molluscs, items13,14. But based on present study it was inferred that in
fishes, plant materials, and semi digested materials in the gut addition to animal based diets, diatoms (9.52 %) and green
contents in which crustaceans were found more and rest group algae (9.52 %) were also accepted by this fish, during the
followed the same priority orders13,14. However, in the present scarcity of animal origin food. Among the semi-digested
study the same food groups were observed, but the difference materials (11.63 %) dry leaves, small stems, plant twigs, scales
was noticed in respect of (%) occurrence and total point. This etc were also noticed in addition to sand and mud. Moreover,
could be attributed to the fact that abundance and type of food The zooplanktons, cyclops, daphnia, insect's body parts, larvae
items greatly depends upon the nature of the habitat in which and pupae as the primary food while plant diet as the secondary
fish accommodates. Hence the lowest value was recorded of food, sand and oligochaetes were the incidental food and the
amphibians (tadpoles), and annelids, due to the fact that fish scales were the emergency food12.
tadpoles were available only during the months of July to Monthly variations in the average Ga.SI values depicted that
September while the availability of annelids (small earthworms), during March, April and May the values get elevated and showed
was rare. highest or first peak (6.539) in May (fig.1a). This could be
The monthly variations on the basis of average index of fullness, attributed to the fact that, this period (February to May) is
average points/fish and (%) empty stomachs revealed that considered as the pre-breeding season of the fish, which
during February, all the guts were non empty with an average corresponded to gonad maturation and therefore high energy
index of fullness 4.61 and 11.21 average points/fish while, from is required for attaining sexual maturity. As a result during this
March to May only few stomachs were empty. But the season fish became highly voracious in nature leading to rise
maximum number of empty stomachs were obtained during in Ga.SI values. But after that, the trend line showed
June (63.16 %), July (73.68 per cent) i.e., breeding period. depression, during the month of June (4.381) and July (4.529)
Further, the (%) of empty stomachs was decreased during as during breeding period the feeding activity became low.
August, but yet it was higher as compared to September and Further there was little increment of Ga.SI value in August,
October. It clearly indicated that, amount of food acceptance which itself explained the low feeding activity during parental
varied with seasonal changes as well as the periods of sexual care. But after that the feeding activity, became normal as fish
cycle (pre breeding, breeding and post breeding season). During adopted voracious nature of feeding to resume the spent
the breeding period (June, July) the presence of maximum energy. Hence the second highest peak was recorded during
empty stomachs indicated decreased feeding rate and feeding September (5.876) after which it declined due to fall in
intensity, which was followed by August, i.e., period of parental temperature. The evaluation of average Ga.SI value's for different
care. An inverse relationship between feeding and breeding size groups (Fig.1.b) depicted that both sexes did not show
cycles has been reported by many workers26, 27 and confirmed much differences accept few exceptions, which proved that
the present findings. The seasonal changes in food and feeding both sexes have equally voracious nature at any size, during
habits have also been reported by some investigator12,14,28. It their life period. However, 60-80 mm group exhibited the highest
(309) Koundal, Koundal, Sharma and Dhanze

Ga.SI value's, in both the sexes, which could be attributed to 8. Lee, P. G. and Ng, P. K. L. (1991). Nature Malaysiana., 16
the fact that female at this size range, was found to be in 'pre- (4): 113.
breeding' stage while male fish, showed first sexual maturity 9. Prasad, A., Nataranjan, M., Gupta, S. C. and Chandra, R.
as such fed less than the female of that size. Moreover, this (1987). Indian Veterinary Research Institute, Izatnagar,
period of poor feeding coincided with the peak spawning India,4: 277.
season, as the maximum numbers of empty stomachs were 10. Rao, L. M., Ramaneswari, K. and Rao, L. V. (1998). Ind.
also recorded (fig.1.a). It has been reported that feeding intensity J. Fish., 45(3): 349.
was very poor in case of mature fish and confirmed the present
11. Dasgupta, M. (2000).Ind. J. Fish., 47(3): 265.
views14.
12. Saxena, A. (2000).U. P. J. Zool., 17.:18.
T h u s t h e p r e s C. punctata (Bloch)
e n t f i n d i n g s c o n f i r m e d t h a t

13. Nazrul, M. I., Shahanaz, P., Hyder, F. and Fawiza, A. (2004).


is highly voracious carnivorous fish at any size, and its feeding
J. Biol. Sci. Flora., 3(2): 352.
activity could change drastically, during the different periods
of sexual maturity. The feeding intensity of this fish decreases 14. Bhuiyan, A. S, Afroz, S. and Zaman, T. (2006). J. Life Earth
during the months of June-July i.e. the breeding period and Sci., 1(2): 53.
after that it again adopts its voracious nature. 15. Guseva, L. N. (1990). J. Ichthyol., 30(4): 11.
16. Arul, V. (1991). Aquacult.Fish. Manage., 22(1): 423.
ACKNOWLEDGEMENTS 17. Ahmed, I.(1993).In: Influence of pond size, artificial feed
The authors are grateful to Director, Zoological Survey of India, and Tilipia mixed culture on the growth performance of
Kolkata and Officer-in-Charge HARC, ZSI, Solan for facilities Channa marulius in the fertilized ponds. Department of
and encouragement. We are thankful to the Dean, COVAS, Zoology and Fisheries, University of Agriculture,
CSKHPKV, Palampur for providing facilities. Faisalabad, Pakistan. 152 p.
18. Mohanty, S. S. and Samantaray, K. (1996). J. Aqua,. 4(1): 37.
REFERENCES 19. Jianguang, Q. and Fast, A. W. (1996). Aquaculture., 144
1. Vander, Z., Shuter, B. J., Lester, N. P., and Rasmussen, J. (4): 313.
B. (2000). Can. J. Fish. Aquat. Sci., 57: 725. 20. Congxin, X., Chuanxi, X., Zhou, J., Xinmiao, W., and Hui,
2. Alam, M. M. and Parween, S. (2001). Pak. J. Zool., 33(3) : 259. J. (1997). Acta hydro. Sinica., 2(3): 213-218.

3. Dambo, W. B. and Rana, K. J. (1992). Aquacult.Fish. 21. Choudhury, M. and Biswas, S. P. (2004). J.Inland Fish.
Manag., 23(1): 71. Soc. India., 36(2): 65.

4. Munshi, J. S. D. and Hughes, G. M. (1992). In: Air breathing 22. Windell, J. T. and Bowen, S. H. (1978). In: Methods for the
fishes of India. Their structure, function and life history: Assessment of Fish production in freshwater, Third
Rotterdam, A. A. Balkema., 338 p. edition, (Bagnel T,ed) Oxford. Blackwell Scientific
Publications, 219-226 p.
5. Gosh S. (2006). Composition and distribution of lipids
and fatty acids in two local fishes of West Bengal. In: 23. Crisp, D. T., Mann, R. H. K., and McCormack, J. C. (1978).
Ph.D thesis, University of Calcutta. J. Fish. Biol., 12(1): 287.

6. Kumar, D. (1992). Fish Culture in undrainable ponds - A 24. Kow, T. A. (1950). In: The food and feeding relationships
manual for extension. FAO: Fisheries Technical Paper. of the fishes of Singapore Straits. Colonial Office Fishery
ISBN: 9251031398, ISSN: 0429-9345., http://www.fao.org/ Publications, U.K. 1(1).1-35 p.
DOCREP/003/T0555E/T0555E00.html. 25. Hynes, H. B. N.(1950). J. Anim. Ecol., 19(1): 36.
7. Kuppulakshmi, C., Prakash, M., Gunasekaran, G., 26. Pandian,T. J.(1966). Ind. J. Fish., 13(1-2): 322.
Manimegalai, G., and Sarojini, S. (2008). European 27. Pantulu, V. R. (1961). Proc. Nat. Inst. Sci. India., 27(1):
Review for Medical and Pharmacological Sciences., 198-225.
12(3): 149.
28. Dewan, S. and Shaha, S. N. (1979). Beng. J. Zool., 7(2): 75.

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