Larval and early juvenile development of Paralomis granulosa reared at different temperatures: tolerance of cold and food limitation in a lithodid crab from high latitudes

Paralomis granulosa Jacquinot is a commercially fished lithodid crab species living in subantarctic and cold-temperate regions of southern South America. Its larval stages (Zoea I, II, Megalopa) are fully lecithotrophic, developing in the complete absence of food from hatching through metamorphosis; first feeding occurs in the first juvenile crab stage. In laboratory rearing experiments conducted at constant 1, 3, 6, 9, 12, and 15°C, we studied rates of larval and early juve- nile survival and development in relation to temperature. At 1°C, many larvae (52%) reached the Megalopa stage almost 2 mo after hatching, but all died subsequently without passing through meta- morphosis. Larval development was successfully completed at all other temperatures, with maximum survival at 6 to 9°C. The time of non-feeding larval development from hatching to metamorphosis lasted, on average, from 24 d (at 15°C) to almost 4 mo (117 d, at 3°C). When the experiment was ter- minated 1 yr after hatching, the 3rd (3°C) to 8th (15°C) juvenile crab instar had been reached. The relationship between the time of development through individual larval or juvenile stages (y) and temperature (T) was described as a power function (y = a × T b , or log(y) = log(a) + b · log(T); the same regression model was also used to describe the temperature-dependence of cumulative periods of development from hatching. The wide thermal tolerance window for successful larval development (at least 3 to 15°C) and the broad geographic range of this species show that the early life-cycle stages of P. granulosa are cold-eurythermal. This physiological trait together with larval independence of food indicate that this lithodid crab species is well adapted to severe conditions of cold in com- bination with the food-limitation in subantarctic regions. Since similar traits have been also observed in other Lithodidae, we suggest that early life-history adaptations to low temperatures and low plank- tonic productivity may explain the high number of lithodid species occurring at high latitudes and in the deep sea, i.e. in conditions under which other Decapoda show strongly reduced diversity.

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