Both larvae and juveniles were cultured under static conditions,
seawater in the cylindro-conical tank being moderately aerated
and fully renewed every 1–2 days with 1-μm filtered and UV-treated
seawater at a mean temperature of 15.5 ± 0.4 °C (±SD). During the
post-set period, the upwelling water motion by aeration also facilitated
water exchange between the inside and outside of the settlement tray.
Larvae were fed predominantly a bi-algal diet of CC+ TL and juveniles
with CM + TL (both mixed at a 1:1 ratio by ash-free dry weight,
AFDW) at 1–2 × 104 and 2–5 × 104 equivalent TL cells by AFDW
(E-TL) ml−1 d−1, respectively. A photoperiod of 16-h light and 8-h
dark, using overhead cool-white fluorescent lights, was used throughout
Both larvae and juveniles were cultured under static conditions,seawater in the cylindro-conical tank being moderately aeratedand fully renewed every 1–2 days with 1-μm filtered and UV-treatedseawater at a mean temperature of 15.5 ± 0.4 °C (±SD). During thepost-set period, the upwelling water motion by aeration also facilitatedwater exchange between the inside and outside of the settlement tray.Larvae were fed predominantly a bi-algal diet of CC+ TL and juvenileswith CM + TL (both mixed at a 1:1 ratio by ash-free dry weight,AFDW) at 1–2 × 104 and 2–5 × 104 equivalent TL cells by AFDW(E-TL) ml−1 d−1, respectively. A photoperiod of 16-h light and 8-hdark, using overhead cool-white fluorescent lights, was used throughout
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