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Table 7.

Competitive and global linear models examined to explain variation in size of 69 square-root-transformed seasonal ranges (95% fixed-kernel home-range contour, SR) and square-root-transformed daily core areas (50% fixed-kernel home-range contour, SCA) for 16 adult male and 12 adult female Cooper's hawk on two north Florida study areas, 1996–2000. Model ranking was based on Akaike's Information Criterion (AIC) corrected for small sample size (AICc). All competitive models (within 2 AIC units of the top model) and the global model are shown. Models were fit with an identity link function.

Competitive and global linear models examined to explain variation in size of 69 square-root-transformed seasonal ranges (95% fixed-kernel home-range contour, SR) and square-root-transformed daily core areas (50% fixed-kernel home-range contour, SCA) for 16 adult male and 12 adult female Cooper's hawk on two north Florida study areas, 1996–2000. Model ranking was based on Akaike's Information Criterion (AIC) corrected for small sample size (AICc). All competitive models (within 2 AIC units of the top model) and the global model are shown. Models were fit with an identity link function.
Competitive and global linear models examined to explain variation in size of 69 square-root-transformed seasonal ranges (95% fixed-kernel home-range contour, SR) and square-root-transformed daily core areas (50% fixed-kernel home-range contour, SCA) for 16 adult male and 12 adult female Cooper's hawk on two north Florida study areas, 1996–2000. Model ranking was based on Akaike's Information Criterion (AIC) corrected for small sample size (AICc). All competitive models (within 2 AIC units of the top model) and the global model are shown. Models were fit with an identity link function.
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