This study aimed to investigate the feeding behaviour (particularly gut fullness and evacuation, preying on rotifers and feeding preference in the water column) of the calanoid copepod, Pseudodiaptomus hessei, as a potential live feed species for aquaculture. Fed and starved, male and female P. hessei were fed rotifers (Brachionus plicatilis) in the presence and absence of microalgae for 24 hr. Starved copepods consumed more rotifers (11.31 ± 1.01, individual rotifers) than fed (8.06 ± 1.01, individual rotifers) while the number of rotifers consumed in the presence of microalgae was similar when fed or starved. Gut fullness and evacuation was determined by feeding copepods two different cell size microalgae species (Tetraselmis suecica and Isochrysis galbana). Gut fullness and evacuation percentage were observed under the dissecting microscope (as 0, 25, 50, 75 and 100%). Copepods fed on T. suecica (large cell) filled their guts more rapidly, while those fed on I. galbana (small cell) evacuated their guts faster. Feeding preference was determined using a multifactorial experiment where copepods were fed two microalgae species, T. suecica and I. galbana, each presented as benthic and planktonic food sources. P. hessei preferred to feed on planktonic microalgae first regardless of microalgae choice species for ±80 min, before shifting to benthic food source. This information can be used as baseline information for aquaculturists to rear the species as live feed for marine fish larvae.
Reducing the time to settlement and metamorphosis of abalone larvae is critical for ensuring that abalone larvae settle within the seeding site for ocean ranching or to increase production in hatcheries. This study investigated the effect of biological (planktonic Nitzschia sp.) and chemical (potassium chloride) cues in inducing settlement and metamorphosis of abalone larvae Haliotis midae on diatom‐coated plastic sheets. Larvae were exposed to different concentrations of KCl (10–20 mM), with settlement being highest at 10 mM in the first 20 h. Settlement of larvae exposed to a combined KCl and Nitzschia treatment for 24 h was highest, followed by larvae exposed to KCl for 12 h, while larvae exposed to KCl for 24 h, and both controls (12 and 24 h) had the lowest settlement. However, in both experiments, larval settlement in all treatments declined after 24 h of exposure, while that of the controls (no added settlement cues) increased and surpassed the other treatments after 24 h. Finally, the settlement was very low on uncoated sheets, compared to diatom‐coated sheets, regardless of exposure to different combinations of KCl and Nitzschia. The exposure period's results should be interpreted with caution when drawing biological conclusions for field studies. This is due to the dramatic decrease in mean settlement post‐exposure to the cue. Therefore, we hypothesize that exposure of H. midae larvae to 10 mM KCl and Nitzschia sp. will not enhance settlement in the ocean, as the inducers are primarily only effective at a KCl concentration level equal to 10 mM for 12 h. However, long‐term exposure to KCl and Nitzschia over 24 h could be used in hatcheries to improve the settlement of H. midae larvae.
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