Farming carps in leased ponds, Bangladesh - Library - NACA
Farming carps in leased ponds, Bangladesh - Library - NACA
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