1998
DOI: 10.1016/s0044-8486(97)00223-8
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Factors affecting the food value of diatom strains for post-larval abalone Haliotis iris

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Cited by 69 publications
(45 citation statements)
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“…Individuals of a cohort, alike in age and grown under the same conditions, present a heterogeneous distribution of sizes. Examples have been described for clams (Malinowski 1988), oysters (Pit and Souhgate 2003), abalone (Kawamura et al 1998;Mgaya and Mercer 1995;Steinarsson and Imsland 2003;Heath and Moss 2009), among others. Given the variances in the growth rates, a cohort attains a specific market size in different spans, which affects the efficiency of production (Malinowski 1988).…”
Section: Introductionmentioning
confidence: 99%
“…Individuals of a cohort, alike in age and grown under the same conditions, present a heterogeneous distribution of sizes. Examples have been described for clams (Malinowski 1988), oysters (Pit and Souhgate 2003), abalone (Kawamura et al 1998;Mgaya and Mercer 1995;Steinarsson and Imsland 2003;Heath and Moss 2009), among others. Given the variances in the growth rates, a cohort attains a specific market size in different spans, which affects the efficiency of production (Malinowski 1988).…”
Section: Introductionmentioning
confidence: 99%
“…For instance, Kawamura & Takami (1995) reported very low digestion efficiency (8.5%) for a certain species of Nitzschia. In a subsequent study, however, Nitzschia ovalis was observed to have a digestion efficiency of 32.3% while another species of Nitzschia had a rather high digestion efficiency of 92.7% (Kawamura et al, 1998). These studies simply demonstrate the varying digestion efficiencies among different species of Nitzschia alone and possibly similar nature or disposition may hold true for other diatom species.…”
Section: Introductionmentioning
confidence: 79%
“…These cues can be an appropriate substrate (Woodin, 1991;Hadfield et al, 1994), a food source (Hadfield, 1978;Garland et al, 1985) or a biochemical signal (Hadfield, 1977;Pavlik, 1992). Benthic diatoms are important components in the haliotid diet where extracellular substances from these microalgae served as essential food of the young postlarval abalone (Kawamura & Takami, 1995;Kawamura, 1996;Takami et al, 1997a, Kawamura et al, 1998. The inductive effects of the chemical compound, GABA, on the larval settlement and metamorphosis of temperate, semi-tropical or tropical abalone species are well documented (see Morse et al, 1979;Morse & Morse, 1984;Barlow, 1990;Searcy-Bernal et al, 1992;Yang & Wu, 1995;Roberts & Nicholson, 1997;Searcy-Bernal & Anguiano-Beltran, 1998;Bryan & Qian, 1998;Gapasin & Polohan, 2004).…”
Section: Introductionmentioning
confidence: 99%
“…A limited number of diatoms showed high digestion efficiencies and induced rapid growth in larger postlarvae 14,15,28 . Attachment strength of diatoms was one of the factors that affected the diatom digestibility for postlarval abalone.…”
Section: Changes In Digestibility Of Diatomsmentioning
confidence: 99%