Table 1.
Hypotheses | Proposed process | Implicated bioclimatic variable(s) considered in this study |
---|---|---|
Heat balance | Large body size advantageous for thermoregulation in cold environments because increases thermal inertia (Olalla-Tárraga & Rodríguez, 2007) | Mean temperature |
Endurance | Large body size favoured in areas with high thermal excursion, because it is associated to more fat reserves (Ashton, 2002) | Thermal excursion |
Seasonality | Large body size favoured in areas with long growing season (Mousseau, 1997, Schutze & Clarke, 2008) | Temperature, thermal excursion, precipitation seasonality* |
Starvation resistance | Large individuals have more reserves and can better survive during periods of food shortage, thus large body size is favoured in seasonal/cold environments where animals are inactive for long periods (Arnett & Gotelli, 2003, Ashton & Feldmann, 2003) | Temperature, thermal excursion, precipitation seasonality* |
Water availability | Large body size is favoured in dry climates because it reduces desiccation tolerance (Ashton, 2002) | Precipitation, aridity |
Primary productivity | Evolution of large body size favoured in more productive environments, where food supply is higher (Olalla-Tárraga & Rodríguez, 2007, Ficetola et al., 2010) | Normalized Difference Vegetation Index (NDVI) |
*amphibian activity depends on both temperature and water availability