1 1.10 Application of estuarine and coastal classifications in marine ...
1 1.10 Application of estuarine and coastal classifications in marine ...
1 1.10 Application of estuarine and coastal classifications in marine ...
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distributions, both with<strong>in</strong> <strong>and</strong> surround<strong>in</strong>g their jurisdictions. Spatial characterizations can be<br />
species-centered, biological community centered, can represent bioregions <strong>and</strong> can be derived<br />
from geophysical or chemical variables <strong>and</strong> more recently have extended to characterize human<br />
use patterns <strong>and</strong> threats to ecosystems. The most common data types used for basel<strong>in</strong>e<br />
characterizations <strong>in</strong> the mar<strong>in</strong>e environment are benthic habitat maps <strong>and</strong> l<strong>and</strong>cover maps <strong>in</strong><br />
terrestrial environments. Thematic habitat maps are typically developed from <strong>in</strong>terpretation <strong>of</strong><br />
remotely sensed data (space-, air- or ship-based) guided by georeferenced <strong>in</strong> situ samples to<br />
def<strong>in</strong>e classes or through spatial <strong>in</strong>terpolation <strong>of</strong> georeferenced <strong>in</strong> situ samples. In many<br />
<strong>in</strong>stances the ecological relevance <strong>of</strong> mapped classes is unclear <strong>and</strong> much work is required to<br />
determ<strong>in</strong>e the relationship between the spatial distributions <strong>of</strong> habitat classes <strong>and</strong> the distribution<br />
<strong>of</strong> other ecological attributes <strong>in</strong>clud<strong>in</strong>g species <strong>and</strong> biological communities.<br />
In the Bahamas, Mumby et al. (2008) found that approximately 25-30% <strong>of</strong> benthic<br />
<strong>in</strong>vertebrate species <strong>and</strong> fish were associated with a s<strong>in</strong>gle habitat class, yet they determ<strong>in</strong>ed that<br />
all classes (n=11) were needed if the management objective was to represent all species <strong>in</strong> the<br />
seascape. In the same region, Harborne et al. (2008) found that although each habitat class<br />
supported a dist<strong>in</strong>ct assemblage <strong>of</strong> fish, the efficacy <strong>of</strong> mapped habitats as surrogates for fish<br />
communities was limited by <strong>in</strong>tra-habitat variability that <strong>in</strong>creased with geographical scale. The<br />
relevance <strong>of</strong> mapped classes to biological communities, however, can be dependent on the<br />
mapp<strong>in</strong>g tools applied <strong>and</strong> the variables measured. In southern Engl<strong>and</strong>, Eastwood et al. (2006)<br />
determ<strong>in</strong>ed that benthic <strong>classifications</strong> <strong>of</strong> s<strong>of</strong>t sediments derived from side-scan sonar were not<br />
effective at classify<strong>in</strong>g biological assemblages. Similarly, Stevens <strong>and</strong> Connolly (2004) found<br />
that abiotic surrogates classified from underwater video transects <strong>in</strong> Moreton Bay, Australia,<br />
were not good surrogates for patterns <strong>of</strong> mar<strong>in</strong>e biodiversity. In northern Australia, however,<br />
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