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Final Technical Report: - Southwest Fisheries Science Center - NOAA

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2.0 Background<br />

The Navy and other military users of the marine environment are required to assess the<br />

impact of their activities on marine mammals to comply with the Marine Mammal Protection<br />

Act, the Endangered Species Act, and the National Environmental Policy Act. The number of<br />

marine mammals that might be impacted by Navy activities must be estimated in any such<br />

Environmental Assessment or Environmental Impact Statement. However, existing marine<br />

mammal density data are typically estimated for areas that are much larger than the area of<br />

interest for a naval exercise. For example, the Navy might be interested in knowing the number<br />

of whales and dolphins in a portion of their Southern California Offshore Range (SCORE), and<br />

density estimates are only available collectively for all of California’s offshore waters.<br />

Stratification to estimate density in smaller areas is not effective because the number of sightings<br />

is typically not sufficient to make an estimate. Clearly, a method is needed to estimate cetacean<br />

density on a finer geographic scale. Also, marine mammal densities are known to change as a<br />

function of the oceanographic variables that define their habitat, and historical densities might<br />

not be the best estimates of current or projected density. There is therefore a need to predict<br />

marine mammal density based on measured or projected oceanographic conditions. In addition<br />

to their need for absolute estimates of marine mammal density (the expected number of animals<br />

per square km), the Navy also could use relative measures of marine mammal density in<br />

selecting among alternative sites for their training activities.<br />

The development of tools for the statistical analysis of geographic distribution and<br />

abundance has accelerated recently, as evidenced by special issues of two journals dedicated to<br />

this subject (Ecological Modelling 2002, Vol. 157, Issues 2-3 and Ecography 2002, Vol. 25,<br />

Issue 5). Although Generalized Linear Models (GLMs) are still commonly used (Martínez et al.<br />

2003), there is a growing recognition that species abundances should not be expected to vary<br />

linearly with habitat gradients (Austin 2002, Oksanen and Minchin 2002). There is growing<br />

acceptance of non-linear habitat relationships including Huisman-Olff-Fresco and Gausian<br />

models (Oksanen and Minchin 2002) as well as non-parametric Generalized Additive Models<br />

(Guisan et al. 2002, Wood and Augustin 2002). Active areas of current research in this field<br />

include methods of model selection such as ridge regression (Guisan et al. 2002), dealing with<br />

spatial autocorrelations (Keitt et al. 2002, Wood and Augustin 2002), and investigations of the<br />

appropriate scale for modeling (Dungan et al. 2002).<br />

The development of spatially explicit methods of analyzing cetacean line-transect data<br />

has increased rapidly in recent years (see review by Redfern et al. 2006). Reilly (1990) used<br />

multivariate analysis of variance to examine the relationship of dolphin distributions to<br />

environmental variables in the ETP. Reilly and Fiedler (1994) and Fiedler and Reilly (1994)<br />

used canonical correspondence analysis (CCA) to quantitatively determine the relationship<br />

2

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