Jeanne B. Wexler

Tank culture of yellowfin tuna, Thunnus albacares: developing a spawning population for research purposes

Abstract A land-based culture facility for research on yellowfin tuna, Thunnus albacares , was developed at the Achotines Laboratory in the Republic of Panama. Six concrete tanks, and seawater and life support systems were built to maintain a yellowfin broodstock. On average, 50% of the yellowfin caught survived capture and handling, and approximately 30% became broodstock in Tank 1 (17 m diameter, 6 m depth) or Tank 2 (8.5 m diameter, 3 m depth). Each fish was tagged with a microchip implant tag, then weighed, measured, and injected with oxytetracycline (OTC) prior to stocking. Daily rations of primarily market squid, Loligo opalescens , and Pacific thread herring, Opisthonema spp., were regulated based on the feeding activity and energy requirements of the fish. Feeding activity of the broodstock decreased when the water temperatures decreased, and the fish ate decreasing daily rations and increasing calories with increasing size. Spawning occurred in both tanks within 6–8 months of capture. Spawning first occurred in Tank 1 when 24 females ranged in size from 6 to 16 kg and 65 to 93 cm fork length (FL). Spawning was intermittent during the first 2 months and occurred near daily thereafter. Tank size appeared to affect survival rates, the types of mortalities that occurred, and the growth of the fish. Survival rates after 1 year in captivity were higher, and the fish were larger, on average, in Tank 1 than in Tank 2. Most of the mortalities in Tank 1 were the result of wall strikes, which occurred more frequently after the fish reached their highest density of 0.64 kg m −3 and sizes greater than 96 cm FL and 19 kg. Non-linear growth models were fitted to the initial stocking sizes and final sizes of fish that died or were removed from Tank 1 during 1996–1999. Estimated growth rates in length (11–48 cm year −1 ) for fish between 51 and 150 cm FL decreased with increasing length. Estimated growth rates in weight ranged from 9 to 19 kg year −1 for fish less than 19 kg and 20–23 kg year −1 for fish greater than 19 kg. The results of this work demonstrate that the stable environment of a land-based culture facility may be the preferred system for long-term maintenance of a yellowfin broodstock.

Genetic monitoring for spawning ecology of captive yellowfin tuna (Thunnus albacares) using mitochondrial DNA variation

Abstract Mitochondrial DNA genotypes of captive broodstock of yellowfin tuna ( Thunnus albacares ) were compared with those of their offspring in order to monitor spawning frequency and periodicity. Among 38 broodstock individuals, 27 genotypes were observed, 18 of which established a single individuals identity. Spawned eggs and hatched larvae were collected on 48 sampling days over a period of 1 year. Among 538 eggs and larvae analyzed, 10 genotypes were observed; eight of them established a single females identity, and two types were shared by two females. The spawning profiles of these females were determined by observing the occurrence of these genotypes in the offspring. Based on the dates when genotypes first occurred and on growth trajectories estimated for individual fish, the size of a female at first spawning was estimated to be 12–28 kg and 75–112 cm. Usually, multiple females spawned on a given date. The same genotypes were observed on almost any sampling day throughout the year. The results indicated that some individual females were capable of spawning almost daily for extended periods of time as long as they remained in the appropriate range of water temperatures and had sufficient food.

Direct Evidence for Mendelian Inheritance of the Variations in the Ribosomal Protein Gene Introns in Yellowfin Tuna (Thunnus albacares)

Abstract: Restriction fragment length polymorphism found in the S7 ribosomal protein gene introns of yellowfin tuna (Thunnus albacares) was compared between a single pair of parents and their offspring. The sizes of the first intron (RP1) and second intron (RP2) amplified by polymerase chain reaction were 810 bp and 1400 bp, respectively. The dam and sire had different restriction types from one another in HhaI and RsaI digestions for RP1 and in DdeI, HhaI, and ScrFI digestions for RP2. Putative genotypes in both introns of 64 larvae were found to be segregated in Mendelian proportions. Genotype distributions in a wild yellowfin tuna sample (n= 34) were in Hardy-Weinberg proportions, and observed heterozygosity ranged from 0.149 to 0.388. This study presents novel Mendelian markers, which are feasible for tuna population genetic study and pedigree analysis.