Giant trevally Life history
Giant trevally
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Life history
A school of subadult giant trevally in a sandy bay, Hawaii
The giant trevally (ulua) reaches sexual maturity at 54 to 61 cm in length and 3 to 4 years of age, although many authors narrow this down to 60 cm and 3 years of age. Sex ratio estimates from the Hawaiian Islands suggest that the population is slightly skewed toward females, with the male:female ratio being 1:1.39. Spawning occurs during the warmer months in most locations, although the exact dates differ by location. In southern Africa this occurs between July to March, with a peak between November and March; in the Philippines between December and January with a lesser peak during at June; and in Hawaii between April and November with a major peak during May to August. Lunar cycles are also known to control the spawning events, with large schools forming in certain locations at specific phases of the moon in Hawaii and the Solomon Islands. Locations for spawning include reefs, the reef channels and offshore banks. Sampling of schools prior to spawning suggests the fish segregate into schools of only one sex, although the details of this are still unclear. Observations in the natural habitat found spawning occurred during the day immediately after and just before the change of tide when there were no currents. Giant trevally gathered in schools of over 100 individuals, although ripe individuals occurred slightly deeper; around 2 to 3 m above the seabed in groups of 3 to 4, with one silver female being chased by several black males Eventually a pair would sink down to a sandy bottom, where eggs and sperm were released. The fish then diverged and swum away. It appears that that each individual spawns more than once in each period, with only part of the gonads ripe in spawners. Fecundity is not known, although females are known to release several thousand eggs on capture during the spawning process. Eggs are described as pelagic and transparent in nature.
The giant trevally’s early larval stages and their behaviour have been extensively described, with all fins having formed by at least 8 mm of age, with larvae and sub-juveniles being silver with six dark vertical bars. Laboratory populations of fish show a significant variability in the length at a certain age, with the average range being around 6.5 mm. Growth rates in larvae between 8.0 and 16.5 mm are on average 0.36 mm per day. The speed at which larvae swim increases with age from 12 cm/s at 8 mm in length to 40 cm/s at 16.5 mm, with size rather than age a better predictor of this parameter. Size is also a better predictor of endurance in larvae than age. These observations suggest that the species becomes an effective swimmer (is able to swim against a current) at around 7–14 mm. No obvious relationships with age and either swimming depth or trajectory have been found. Larvae appear to also opportunistically feed on small zooplankton while swimming. The larvae actively avoid other large fish, and jellyfish are occasionally used as temporary cover. Larvae have no association with reefs, and appear to prefer to live pelagically. Daily growth is estimated at between 3.82 g/day and 20.87 g/day, with larger fish growing at a more rapid rate. Age at 1 year old is 18 cm, age at 2 years is 35 cm and by 3 years, the fish is around 50 to 60 cm. The use of von Bertalanffy growth curves fitted to observed otolith data shows an individual of around 1 m in length is approximately 8 years old, while a 1.7 m fish would be around 24 years old. The maximum theoretical length of the species predicted by the growth curves is 1.84 m, however the largest reported individual was 1.7 m long. As previously mentioned, as the giant trevally grows it shifts from turbid inshore waters or estuaries to reefs and lagoons in bays, moving finally to outer reefs and atolls. A hybrid of C. ignobilis and C. melampygus (bluefin trevally) has been recorded from Hawaii. The specimen was initially thought to be a bluefin trevally of world record size, however was later rejected when it was discovered to be a hybrid. Initial evidence of hybridisation was morphological characteristics intermediate to the two species, with later genetic tests confirmed that it was indeed a hybrid. It is known the two species school together, including at spawning time, which was considered to be the reason for hybridisation.
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