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Embryonic and Larval Development of the Giant Clam Tridacna noae (Röding, 1798) (Cardiidae: Tridacninae)
Journal article   Open access   Peer reviewed

Embryonic and Larval Development of the Giant Clam Tridacna noae (Röding, 1798) (Cardiidae: Tridacninae)

Paul C Southgate, Richard D Braley and Thane A Militz
Journal of Shellfish Research, Vol.35(4), pp.777-783
2016
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https://doi.org/10.2983/035.035.0406View
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Abstract

giant clam Tridacna noae Tridacninae embryology larval development Papua New Guinea
This paper reports on embryonic and larval development of the giant clam Tridacna noae. Spawning was induced by serotonin injection into the gonad. Unfertilized eggs had a mean (±SE) diameter of 101.14±0.47 mm and spermatozoa heads were 8.92±0.09 mmlong. Embryonic development had progressed to the 8-cell and 16-cell stages by 3 h postfertilization and to the 32-cell stage by 4 h postfertilization. Rotating gastrulae accounted for 82% of developing embryos at 9 h postfertilization. Trochophore larvae accounted for 54% of embryos at 16 h postfertilization, and 98% of larvae at 20 h postfertilization. Straighthinged (D-stage) veligers comprised 74% of developing larvae at 22 h postfertilization with mean (±SE) anteroposterior measurement (APM) of 146.32±0.58 mm, dorsoventral measurement (DVM) of 118.12±0.74 mm, and hinge length of 77.46±0.73 mmat 24 h postfertilization. At 96 h postfertilization, 74% of veligers had settled but had retained the velum without showing development of the foot and, by 120 h postfertilization, 78% of settled veligers had become pediveligers with a probing foot. The mean (±SE) APM of pediveligers at 144 h postfertilization was 176.50±0.97 mm, DVM was 151.86±1.01 mm, and hinge length was 63.50±0.95 mm. Gills were first observed in settled individuals 11 days after fertilization, indicating completion of metamorphosis. The methods used in this study supported successful larval culture of T. noae and provide a basis for large-scale propagation of this species.

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