Successful hatchery production of fish and shellfish seeds for aquaculture depends on the availability of suitable live feed organisms

Kandasamy, D

Mohan, S

Palanichamy, S

CMFRI Digital Repository

TECHNIQUES FOR THE MASS CULTURE OF ROTIFERS AND MOINA D. KANDASAMII S. PALANICHAMYI AND S. MOHANI Central Marine Fisheries Research Institute, Cochin - 682014. INTRODUCTION Successful hatchery production of fish and shellfish seeds for aquaculture depends on the availability of suitable live feed organisms. The rotife-t Br(f ~hi()ItJ,M; sp., clf.I~ docetan, Moina sp. and brine shrimp Artemia sp., ha ve high repl'oduct'v poi:en 'ial, !J.hort geJl~tion period, high nutritiv value and c.apacity to live ,nd grow in higb density. These are favoura bleCliarac ers for the mass eul ,u1' of the fl b V rga:ni:!;ltns und r oontroJ1ed cl'lnditions. Among these sp des B. plW£lisl M. bmdrla{~ ,and A aUna (heterosex and pru'theneo genetic rain) have be n most BU :s.sfully .utilized in fish and shellfish hatcheries all OVal' ,he world. This paper deaJs with he methods for the mass production of rotifers and cladocerans carried out under controlled con-ditions at the Regional Centre of Central Marine Fisheries Research Institute (CMFRI), Mandapam Camp. ROTIFER Rotifers are available in the intertidal regions along the sea coast, brackiswater chan-nels, pools and ponds where they grow naturally. Isolation is done by micropipette method under binocular microscope or through the sub-culture method. Stock cul-ture can be developed within a few days from the isolated culture. MASS CULTURE Techniques for the continuou.s mass cultu.re of euryhalilw rotifer B. plica,tili,q have been developed and perfected. H 'gh pl'es ure filtGI'ed seawater is pumpe-d into a. t.ank and fertiliUld with ground-nut oilcake, urea and super phosphate at ~h.(3 rate nf250g-, 109 and 5g per tonne respectively. This medium. is inoculated with Morella . p, on the same day and the rotifers are in roduced 1000-10000 nos.!] on, tb , second day; vigorouB aeration is:given from the start of the culture since the dense concentration of algae and rotire s requires large quant'ty of oxygen espeoia.lly during night time, C1llcken drops or pig manure can also be used as fertilizers. The planktonic, eU:f..Ypaline <.\fid ftlt.er feed'ng rotifer multiplies very fa t by p!lrthe~ no genesis under ideal condjtion and attains maximum concentr.ation (4 -5 x 105 l'otiferJitre) within 5-7 days. It grOW!! very well at salinity levels .20-80 pp and tem-perature range between 26 and 34°C. It is better to harvest daily .25 to 50% of the culture with a replacement of harvested volume of fresh algal culture. Handnet of:>O micron meshsize may be used for harvesting in the morning hours when they I'each the surface. Harvesting at regular intervals helps the culture for good nia'n ,ena.nce I Present Address: Regional Centreo! C.MF.R.l Mandapam Camp - 623 520 82 A mds cla-tiaJ, tligh sms dA. ized lods con-tut an-lette cul-1ave ~ank 50g, ). on day; ltion ime. ·the-105 tem-fthe :>f60 each ance for a long period and should be carried out during the exponential growing phase with 3 or more eggs attached to the body of the rotifers. The nutritive value of the rotifers will be very high during this stage. The harvested rotifers are washed in clean sea water and may be fed directly as fresh or stored by mixing with 10% glyc-erin in a deep freezer at 14°C for later use. Another method involves culturing Chlorella sp. in a 50 t cement tank with above rate offertilization to achieve 20-40 million cells/ml concentration. These micro algae are filtered and passed into 5 t tanks. They are inoculated with stock rotifers. During unfavourable conditions such as high density of rotifer, low oxygen level and scarcity of food, amictic female produces male. By sexual reproduction, the resting eggs get released and settle at the bottom of the culture tank. These cysts are col-lected along with sediments, dried and stored in the dessicator at room temperature. They can also be stored in a deep freezer at 14°C for 3-4 months. The cysts can be safety transported. the dried cysts hatch out within 36-48 hours after hydration with sea water. The resting cysts can be induced to hatch out by sudden reduction of the . salinity in the culture medium. High temperature reduces the length, width and DLS (distance between lateral spines) of the rotifer. The distance between the median spines (DMS) changes with salinity. The size of the rotifers is bigger (130-l40/u in length) at low temperature (below 20°C) and smaller (100/2l0u) at hig!J.er temperatures. B. plicatilis is more tolerant to temperature and salinity fluctuations. Antibacterial treatment As the rotifer may harbour bacteria such as Vibrio, Pseeudomonas, Moraxella, Cytophaga and Flavo bacterium, antibacterial treatment is required. ~I!l ~ifurstyrenat.e (NFS-Na) at the rate of 5 microgram/ml with ultra violet radiation is most effective. Nutritive value The nutritive value of the rotifers depends on the diet they are given. Microalgal diet such as Chlorella sp. Tetraselmis sp.,Dunaliella sp. give better nutritive values. Marine fish and crustacean larvae require poly unsaturated fatty acids (essential fatty acids) (PUFA) for the developmental stages and these can be met through the enriched rotifers. The high initial algal density enhances the fatty acid enrichment in rotifers. The rotifers can also be enriched by using micro encapsulated (3-5 micro size) par-ticles offish oil (cod liver oil) or any other oil extract from. the marine sources. EAA (Essential aminoacid) such as proline and methionine are rich in rotifers fed with 37.5 x 106 Chlorella sp. cell concentration/ml. Basic amino acids such as histi-dine and lysine are more in 25 x 106 fed rotifers. The nutritional quality of rotifers could vary with different cell densities ofChlorella sp. utilised in the culture system. The yeast (yeast supplemented with fish oil) are fed to increase the nutritional qual-83 ity of rotifer. Concentration of protein at the exponential and stationary phase of , growth in the rotifer varies from 34 to 52% dependingupon feeding treatment. This can meet the protein requirement offish and crustacean larvae (30-50%) . For commercial enrichment, super seleo, dry seleo or protein seleo may be used for 3-6 hours along with fresh water Chiorella sp. or baker's yeast, which contains high quantity of 0:3 PUFA. Several enrichment techniques using yeast, micro encaposultated particles or oil based emulsion are available. Mol A Moina can be collected from brackishwater channels, pools and freshwater ponds. A stock culture can be built up from a single parthenogenetic female. The adult re-leases young ones at the rate of 10-12 nos./day and the young ones become adult in 18-24 hours and begin to reproduce. It is possible to obtain 42,000 nos. within 12 days from a single female. MASS CULTURE The filtered freshwater is pumped into a tank (1-10 tonne) an.d fertilized with ground-nut-oil cake (250g), urea (lOg) and super phosphate (5g) per tonne of water. Freshwater Chlorella sp. is inoculated on the same day with a cell concentration of 30-50 million! ml (5-10 litre/tonne). Vigorous aeration should be provided. On the second day after the water becomes slightly greenish the culture of Moina is inoculated from the stock culture with stocking density of 1-5 nosllitre. The plankton multiply rapidly by feeding on the Chiorella sp. and finer particles of ground-nut-oil cake and attain the maximum concentration of 25,000 - 30,000 nos.llitre within 5 to 7 days. At this stage 30 to 50% of the population can be harvested and replaced by freshwater with proportional amount of the above fertilizer or with Chiorella from a separate tank. Harvesting can be done daily morning or evening, when they swarm at the surface by a zooplankton net. Chlorella sp. bloom can be also be obtained by fertilizing with chickett'drops or pig manure. During'unfavourable conditions such as high population. low oxygen level, scarcity of feed, the parthenogenetic females release the male. Mter mating, the female produces the dormant cyst in the brood-pouch. The released cysts settle at the bottom of the tank and can be collected along with the sediments, dried in the room temperature and stored in an airtight container for 3 to 4 months. This can be easily transported without risk. Embryonic development starts when the dry cysts are hydrated with freshwater. The hatchlings come out within 24-36 hours. Harvesting Harvesting is done by using a zooplankton net in the exponential growing phase when the females start reproducing. Parthenogenetic females containing 8-12 em-bryos in the broodpouch have rich inorganic matter and more nutritive values than 84 ;e of , This Jf 3-high ated .s . A I r . lt in in I) md-ater ion! Jter the yby the ;age vith mk. e by vith ;yof Ices the lUre ·ted lith an females with resting eggs or the males . Harvested Moina are washed with freshwa-ter and fed to the larvae or are preserved by mixing equal volume of 10% glycerin and frozen ones (small blocks) in a deep freezer for future use . Nutritive value Moina fed with fish algae are nutritionally richer in PUFA than the ones grown on yeast or commercial single cell proteins. The enrichment of harvested Moina is essential before feeding the fish and crusta-cean larvae. Enrichment of PUFA (cod liver oil or squid oil) can be done as mentioned for the rotifers. The harvested Moina 200-300 nos.!ml. are mixed with enrichment medium along with freshwater Chlorella sp. for 3·4 hours. Conclusion Since Moina are freshwater parthenogenetic animals the a3 PUFA contents are naturally inadequate to feed the fish and crustacean larvae. So, the enrichment is inevitable. 85 

Techniques for the mass culture of rotifers and moina

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Techniques for the mass culture of rotifers and moina

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