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Dissertation - HQ

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94 Vertical distribution during ontogeny<br />

Vertical shifts cause<br />

horizontal movement<br />

Vertical distribution<br />

vs. vertical migration<br />

where there is enough light to feed but not too much to be seen by<br />

predators becomes deeper and deeper in the course of ontogeny. Finally,<br />

temperature also varies vertically and may affect this trade-off, because<br />

of its influence on metabolic rates 72 : fishes staying deeper in the water<br />

column live in colder environments, have lower metabolic rates hence<br />

need to find less food but also grow more slowly.<br />

Apart from influencing the probability to find food, these vertical<br />

movements also affect how larvae are advected by currents. Indeed, a<br />

shear is often noticeable between fast surface velocities and moderate<br />

flow at depth, because of wind stress at the surface and/or bottom<br />

friction at depth. Actually, most hydrographic variables (i.e. current<br />

speed but also temperature, salinity, etc.) vary faster vertically that horizontally.<br />

Therefore, moving vertically may have dramatic consequences,<br />

even on horizontal advection. For example, in Chesapeake Bay, vertical<br />

diffusion influences the result of an advection model more than horizontal<br />

diffusion does 195 . And, indeed, vertical swimming by oyster larvae<br />

greatly modifies their dispersal routes 196 . On coasts featuring strong<br />

tides, synchronisation of vertical migration with tides is a very efficient<br />

means of transport, either inshore or offshore 197,198 . Ontogenetic vertical<br />

migration may also favour retention, as models suggest either on a<br />

large scale (Georges Bank 84 ) or around a smaller island (Barbados 71 ).<br />

Finally, more theoretical works suggest that exploiting vertical shear is<br />

an efficient strategy to reach a settlement site, especially for larvae not<br />

capable of swimming against the flow 199 .<br />

Most of the data on vertical distribution comes from stratified sampling<br />

by towed plankton nets 71,74,130,200–203 . An alternative for late stage<br />

larvae are stratum-specific light traps 204 , but their limited scope restricts<br />

their use. To understand the results of these methods correctly, it is<br />

important to bear in mind that they describe the vertical distribution of<br />

fish larvae and do not give direct information on their vertical migration<br />

behaviour. If individuals move around but that the overall distribution<br />

of the population stays the same, the range of vertical movement of each<br />

larva would be greater than what is inferred from the distribution 79 . At<br />

the other limit, an ontogenetic shift in distribution toward depth could<br />

be the result of selective mortality in the surface without any movement<br />

by larvae. Therefore caution is advised when interpreting distribution<br />

data and trying to infer the movement of individuals, or even patches,<br />

from it.<br />

In this study we seek to detect and quantify ontogenetic shifts in<br />

the vertical distribution of coral reef fish larvae, and to estimate their<br />

impact on the advection of larvae by currents. We use repeated, large<br />

scale, vertically stratified sampling to capture the vertical distribution<br />

of the population of fish larvae around an oceanic island. Eventually,<br />

an oceanographic model, calibrated by observations on the study site,<br />

is used to advect larvae in a realistic, dynamic flow field and compare<br />

the trajectories of passive and vertically migrating ones. Furthermore,<br />

given the prevalence of depth stratified data and the disparateness of

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