A. Folkvord et al., EARLY-LIFE HISTORY OF HERRING LARVAE IN CONTRASTING FEEDING ENVIRONMENTS DETERMINED BY OTOLITH MICROSTRUCTNRE ANALYSIS, Journal of Fish Biology, 51, 1997, pp. 250-263
Newly hatched autumn-spawned herring larvae Clupea harengus were relea
sed in two 2500-m(3) outdoor mesocosms and reared over a 2-month perio
d. Hydrographic conditions were similar in the two mesocosms, but the
average plankton density was initially more than 10 times higher in me
socosm B compared to mesocosm A (>11(-1) v. <0.11(-1)). Half-way throu
gh the experiment the feeding conditions reversed with three times hig
her average densities in mesocosm A than in mesocosm B (>31(-1) v. sim
ilar to 11(-1)). Herring larvae were sampled with a 0.3-m(2) two-chamb
ered net twice weekly, and survivors were harvested by draining the me
socosms at the end of the experiment. Otolith growth trajectories of i
ndividual larvae were determined by relating radial otolith size with
number of increments from the outer edge of the otolith (days before c
apture). The increment widths during the first 3 weeks after hatching,
including the first-check size, were generally wider among larvae fro
m mesocosm B (relatively good initial feeding conditions) than among t
hose from mesocosm A (poor initial feeding conditions). The otolith gr
owth pattern also confirmed that the surviving herring in mesocosm A b
elonged to the upper size range of larvae in the mesocosm after only 2
-3 weeks from hatching, no such trend was found in mesocosm B. In both
mesocosms the otolith size-al-age indicated that with the present sam
pling gear, herring larvae larger than 20-25 mm were underrepresented
in the net samples. The information obtained from otolith-size-at-age
is compared with other morphometric and biochemical measures of size a
nd condition of larvae obtained throughout the experiment. (C) 1997 Th
e Fisheries Society of the British Isles.