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Mireille Consalvey PhD Thesis - University of St Andrews

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Temporal changes in the microscale distribution <strong>of</strong> pigments can be used<br />

to infer changes in biomass associated with migration (Paterson et al. 1998).<br />

However, LTSEM and pigment sampling is destructive. Non-destructivc remote<br />

sensing (RS) techniques use the optical properties <strong>of</strong> the sediments to make<br />

inferences about the distribution/abundance <strong>of</strong> benthic autotrophs (Paterson et al.<br />

1998). However, RS still requires considerable ground truthing.<br />

1.6.2. Algae got rhythm?: Description <strong>of</strong> migratory work to date<br />

Palmer and Round (1965) and Round and Palmer (1966) provided some<br />

<strong>of</strong> the first detailed descriptions <strong>of</strong> the vertical migratory rhythms <strong>of</strong><br />

microphytobenthos which can be surnmarised:<br />

1) Cells move to the sediment surface during the daylight hours when the<br />

sediment surface is exposed by the tides.<br />

2) Prior to submersion cells migrate away from the surface (also Faur6-Fremiet<br />

1951; Happey-Wood and Jones 1988; Ser6dio et al. 1997; Paterson et al.<br />

1998).<br />

3) Individual species come to the surface at different times and may arrive in a<br />

distinct order (also Paterson 1986) and stay for differing times.<br />

4) Species may appear at the sediment for only a short period before leaving but<br />

may return, hence showing a bimodal presence at the surface<br />

5) There can be a difference in the migratory patters observed at low tide in the<br />

moming, to low tide in the aftemoon<br />

6) Migratory rhythms can be maintained in the absence <strong>of</strong> environmental cues<br />

7) Migratory rhythms can be reset/rephased.<br />

32<br />

tl()n

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