Data from: Body temperature distributions of active diurnal lizards in three deserts: skewed up or skewed down?

1. The performance of ectotherms integrated over time depends in part on the position and shape of the distribution of body temperatures (Tb) experienced during activity. For several complementary reasons, physiological ecologists have long expected that Tb distributions during activity should have a long left tail (left-skewed); but only infrequently have they quantified the magnitude and direction of Tb skewness in nature. 2. To evaluate whether left-skewed Tb distributions are general for diurnal desert lizards, we compiled and analyzed Tb (∑ = 9,023 temperatures) from our own prior studies of active desert lizards on three continents (25 species in Western Australia, 10 in the Kalahari Desert of Africa, and 10 species in western North America). We gathered these data over several decades, using standardized techniques. 3. Many species showed significantly left-skewed Tb distributions, even when records were restricted to summer months. However, magnitudes of skewness were always small, such that mean Tb were never more than 1°C lower than median Tb. The significance of Tb skewness was sensitive to sample size, and power tests reinforced this sensitivity. 4. The magnitude of skewness was not obviously related to phylogeny, desert, body size, or median body temperature. Moreover, formal phylogenetic analysis is inappropriate because geography and phylogeny are confounded (that is, are highly collinear). 5. Skewness might be limited if lizards pre-warm inside retreats before emerging in the morning, emerge only when operative temperatures are high enough to speed warming to activity Tb, or if cold lizards are especially wary and difficult to spot or catch. Telemetry studies may help evaluate these possibilities

Ecological consequences of foraging mode

Desert lizards are typically either widely foraging or sit-and-wait predators, and these foraging modes are correlated with major differences in ecology. Foraging mode is related to the type of prey eaten by lizards. Widely foraging lizards in the Kalahari desert, the Western Australian desert, and the North American desert generally eat more prey that are sedentary, unpredictably distributed, and clumped (e.g., termites) or that are large and inaccessible (inactive scorpions) than do sit-and-wait lizards. In contrast, sit-and-wait lizards eat more prey that are active. Foraging mode also appears to influence the types of predators that in turn eat the lizards. For example, a sit-and-wait snake eats predominately widely foraging lizards. Crossovers in foraging mode thus exist between trophic levels. Widely foraging lizards may also encounter predators more frequently, as suggested by analyses of relative tail lengths; but tail break frequencies are ambiguous. Daily maintenance energetic expenditures of widely foraging lizards appear to be about 1.3-1.5 times greater than those of sit-and-wait lizards in the same habitats, but gross food gains are about 1.3-2.1 times greater. Widely foraging species also have lower relative clutch volumes, apparently in response to enhanced risks of predation. Foraging mode within one species varies with changes in food availability. Physiology, morphology, and risk of predation might generally restrict the flexibility of foraging mode. Because foraging mode constrains numerous important aspects of ecology, any general model of foraging velocity must be complex

How often do lizards "run on empty"?

Energy balance is relevant to diverse issues in ecology, physiology, and evolution. To determine whether lizards are generally in positive energy balance, we synthesized a massive data set on the proportion of individual lizards (N = 18223) with empty stomachs (127 species), representing nine families distributed on four continents, primarily in temperate zone deserts but also in the neotropics. The average percentage of individuals with empty stomachs is low (13.2%) across all species, even among desert lizards, suggesting that most lizards are in positive energy balance. Nevertheless, species vary substantially in this regard (among all species, 0% to 66% of individuals have empty stomachs). Several patterns are detectable among species with unusually high frequencies of empty stomachs. In particular, nocturnal lizards “run on empty” more often on average than do diurnal species (24.1% vs. 10.5%); and this pattern holds even for nocturnal vs. diurnal geckos (21.2% vs. 7.2%, respectively). Several (but not all) top predators have a higher frequency of empty stomachs than do species that feed at lower trophic levels. Diet breadth and body size appear unrelated to frequency of empty stomachs. Widely foraging species sometimes have a high frequency of empty stomachs relative to sit-and-wait species, but patterns vary among continents and appear to be confounded by phylogeny and trophic level. Ant-eating specialists have uniformly low frequencies of empty stomachs. Diurnal termite specialists also have low frequencies of empty stomachs, but nocturnal ones have high frequencies. Lizards from certain families (Gekkonidae [including Pygopodidae], Gymnophthlamidae, and Varanidae) are more likely to have empty stomachs than are those of other families (Agamidae, Iguanidae, Lacertidae, Scincidae, and Teiidae)

Appendix A. Dietary and related data on lizard species.

Dietary and related data on lizard species