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Mireille Consalvey PhD Thesis - University of St Andrews

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Cha ici 8 Oencral Di-scussion<br />

largely be-determined by drying out and compaction <strong>of</strong> the sediments as would<br />

be expected, however, more subtle changes were also occurring and may relate to<br />

taxonomic and/or structural (e. g. cell layering) changes within the bi<strong>of</strong>ilm.<br />

8.3. Appraisal <strong>of</strong> main microphytobenthic sampling techniques used<br />

8.3.1. PAM Fluorescence<br />

The linear relationship shown to exist between minimum fluorescence<br />

and microphytobenthic biomass in the laboratory and in situ has been the basis <strong>of</strong><br />

several studies into microphytobenthic migration (see Ser6dio et al. 1997,2001;<br />

Honeywill 2001). In this study changes in F,, 15 at the sediment surface followed<br />

the broadly expected patterns <strong>of</strong> microphytobenthic migration and proved to be a<br />

valuable remote sensing tool.<br />

However, the limitations <strong>of</strong> the technique must also be considered. Whilst<br />

the linear nature <strong>of</strong> the relationship between chlorophyll a and<br />

dark level<br />

minimum fluorescence has been shown (Ser6dio et aL 1997; Barranguet and<br />

Kromkamp 2000; Honeywill 2001; Scr6dio et al. 2001; Honeywill et al. 2002)<br />

the slope and intercept <strong>of</strong> the line are open to variation (Ser6dio et al. 1997).<br />

Therefore the chlorophyll a content per se cannot be inferred from this<br />

technique. Furthen-nore no inference can be made with reference to changes in<br />

the depth distnbution within this zone. In a situation with identical biomass the<br />

distance <strong>of</strong> cells from the surface, as well as their orientation, may alter the<br />

relationship between F, 15 and biomass (Figure 8.1 A, B and C). Also in a<br />

situation <strong>of</strong> high biomass (Figure S. ID) there are additional questions relating to<br />

237

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