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Farming carps in leased ponds, Bangladesh - Library - NACA

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Mar<strong>in</strong>e F<strong>in</strong>fi sh Aquaculture<br />

Magaz<strong>in</strong>e<br />

An electronic magaz<strong>in</strong>e of the<br />

Asia-Pacifi c Mar<strong>in</strong>e F<strong>in</strong>fi sh<br />

Aquaculture Network<br />

Contact<br />

Asia-Pacifi c Mar<strong>in</strong>e F<strong>in</strong>fi sh<br />

Aquaculture Network<br />

PO Box 1040<br />

Kasetsart Post Offi ce<br />

Bangkok 10903, Thailand<br />

Tel +66-2 561 1728 (ext 120)<br />

Fax +66-2 561 1727<br />

Email grouper@enaca.org<br />

Website http://www.enaca.org/<br />

mar<strong>in</strong>efi sh<br />

Editors<br />

Koji Yamamoto<br />

Asia-Pacifi c Mar<strong>in</strong>e F<strong>in</strong>fi sh<br />

Aquaculture Network<br />

c/o <strong>NACA</strong><br />

sim@enaca.org<br />

Dr Michael J. Phillips<br />

Environmental Specialist &<br />

Manager of R&D, <strong>NACA</strong><br />

Michael.Phillips@enaca.org<br />

Simon Wilk<strong>in</strong>son<br />

Communications Manager<br />

simon.wilk<strong>in</strong>son@enaca.org<br />

Dr Mike Rimmer<br />

Pr<strong>in</strong>cipal Fisheries Biologist<br />

(Mariculture & Stock<br />

Enhancement)<br />

DPIF, Northern Fisheries Centre<br />

PO Box 5396<br />

Cairns QLD 4870<br />

Australia<br />

Mike.Rimmer@dpi.gov.au<br />

January-March 2006<br />

Larval rear<strong>in</strong>g<br />

Rear<strong>in</strong>g methodologies were <strong>in</strong>itially<br />

developed from small-scale replicated<br />

experiments used to address issues<br />

dur<strong>in</strong>g the early larval stages. However,<br />

larval survival <strong>in</strong> small-scale recirculation<br />

systems is poor with 100%<br />

mortality common by day 10. Physical<br />

parameters identifi ed dur<strong>in</strong>g smallscale<br />

trials were transferred to a larger<br />

pilot scale rear<strong>in</strong>g trial us<strong>in</strong>g mesocosm<br />

technology. The same protocol has<br />

been used to produce fi ngerl<strong>in</strong>gs of two<br />

grouper species with diffi cult early life<br />

stages.<br />

Tank management<br />

Newly fertilised eggs (day 0) were<br />

stocked at a density of 30/litre <strong>in</strong>to a<br />

6m³ fi breglass mesocosm system. Water<br />

was exchanged dur<strong>in</strong>g days 1-2 at 5%<br />

tank volume per hour dur<strong>in</strong>g the day.<br />

No water was exchanged on days 3-4<br />

to prevent the removal of prey, particularly<br />

copepod nauplii, from the tank<br />

dur<strong>in</strong>g the critical fi rst feed<strong>in</strong>g period.<br />

From day 5, water was exchanged overnight<br />

start<strong>in</strong>g at 5% per hour, <strong>in</strong>creas<strong>in</strong>g<br />

to 11% per hour with cont<strong>in</strong>uous<br />

fl ow from day 17 post-hatch<strong>in</strong>g.<br />

Squid oil was added to the water<br />

surface twice daily from day 1 to 6<br />

post-hatch<strong>in</strong>g to prevent larvae from<br />

becom<strong>in</strong>g caught <strong>in</strong> the water surface<br />

tension. A photophase of 12 hours of<br />

light and 12 hours of dark was supplied<br />

by two overhead daylight fl uorescent<br />

tubes supplemented by a low level of<br />

natural light. Light <strong>in</strong>tensity ranged be-<br />

Mar<strong>in</strong>e F<strong>in</strong>fi sh Aquaculture Network<br />

tween 300 and 700 lux across the tank<br />

water surface.<br />

Feed<strong>in</strong>g schedule<br />

Four microalgal species (Tetraselmis<br />

sp., Cryptomonad sp., Isochrysis sp.<br />

(T.ISO) and Nannochloropsis oculata)<br />

were added daily from day 0 to 22.<br />

They were added on an equal ration<br />

(organic weight) basis to ma<strong>in</strong>ta<strong>in</strong> an<br />

algal concentration equivalent to 2.2<br />

x 105 N. oculata cells/ml -1 . On day<br />

2 post-hatch<strong>in</strong>g, copepods (Acartia<br />

s<strong>in</strong>jiensis) and super-small stra<strong>in</strong> rotifers<br />

(B. rotundiformis) were added at<br />

densities of 1.25/ml -1 and 10/ml -1 , respectively.<br />

Enriched rotifers (Algamac<br />

2000) were added from day 6 until day<br />

16 to ma<strong>in</strong>ta<strong>in</strong> a density of 15 to 20/ml -<br />

1 . Artemia nauplii were <strong>in</strong>troduced<br />

from day 9 - 13 and enriched (Algamac<br />

3050) meta-nauplii from day 13 - 28.<br />

Artifi cial diets were <strong>in</strong>troduced from<br />

day 9 onwards as detailed <strong>in</strong> Figure 1.<br />

Metamorphosis/<br />

cannibalism<br />

The fi rst metamorphosis of larvae to<br />

juveniles was noted on day 29-30 for<br />

both species and the majority had metamorphosed<br />

by day 40. Growth rates<br />

were similar for both species dur<strong>in</strong>g the<br />

larval phase with a slight <strong>in</strong>crease <strong>in</strong><br />

gold-spot cod growth rates compared to<br />

that of fl owery cod dur<strong>in</strong>g the juvenile<br />

phase. Cannibalism co<strong>in</strong>cided with the<br />

start of metamorphosis and was the major<br />

cause of mortality. Grouper larvae<br />

are very sensitive to handl<strong>in</strong>g stress<br />

Figure 2. Total length (mean value and standard error) of fl owery cod<br />

(open circles) and gold-spot cod (closed squares).<br />

35

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