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Acknowledgements 91<br />

This evidence and the lack of correlation with physical variables,<br />

except for a possible accumulation in the atoll’s lee or in eddies, suggest<br />

that larval distribution was determined by the combined effects of advection<br />

by currents, spawning time (because it determines which currents<br />

the larvae will be subjected to), and family-specific swimming strategies<br />

interacting with the current. Indeed larvae did not seem to position<br />

themselves in areas of specific hydrographic or feeding conditions, so<br />

their swimming was probably more related to the interaction with, and<br />

exploitation of, flow structures. And at least some larvae probably swam<br />

because some Pomacentridae larvae, for example, were found more<br />

than 20 km away from the nearest shore (while species with demersal<br />

eggs were thought to stay close to shore 162,168 ). If those larvae were to<br />

recruit, Tetiaroa was the nearest opportunity, and it would demand<br />

some significant swimming to get there.<br />

. . . and this is<br />

a behaviourally<br />

driven process<br />

In a nutshell, no strong biophysical correlates could actually be<br />

detected between the overall distribution of coral reef fish larvae and<br />

hydrographic factors such as temperature, phytoplankton richness, or<br />

local current speed. No general “law” regarding the spatial position of<br />

larval aggregations was obvious either (close or far from shore, on the<br />

windward or leeward side of land masses, etc.). This lack of evidence<br />

could be caused by the limitations of currently available sampling<br />

methods which do not resolve both metre and kilometre scale structures<br />

at once. Such limitations will only be overcome by instruments allowing<br />

both high frequency and large scale sampling, such as towed video<br />

recording systems 188 . Alternatively, the spatial distribution could be the<br />

result, seemingly random and probably chaotic, of advection by currents<br />

together with behaviour by fish larvae. The only way to predict the<br />

distribution of larvae in such a situation is probably that used in Paris<br />

& Cowen 71 : small temporal and spatial scale modelling with immediate<br />

feedback from observations. Only by progressing in small time steps is it<br />

possible to resolve such non-linear interactions between behaviour and<br />

currents. While the advances in physical oceanography are promising,<br />

predicting larval advection accurately will remain impossible until we<br />

gain, at least, a clear understanding of the behaviour of fish larvae<br />

throughout ontogeny.<br />

4.A Acknowledgements<br />

The authors are grateful to the captain and crew of the N. O. Alis who<br />

showed unweary enthusiasm and ingenuity, to the rest of the scientific<br />

crew (C. Guigand, L. Carassou, D. Lecchini, P. Ung), to R. K. Cowen<br />

for accepting to lend his equipment and let go some of his best crew<br />

members for a month, to P. Torres for his help with the sorting of<br />

MOCNESS samples, to A. Fukui, D. Johnson, J. M. Leis, M. J. Miller,<br />

D. Richardson, and A. Suntsov for their advice on the identification of<br />

fish larvae, and to the staff of the CRIOBE, in Moorea, for pre- and post-

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