We have previously shown that ecological habit (e.g., arboreal, terrestrial, amphibious) correlates with thermoregulatory behaviors and water balance physiology among species of hylid frogs in northern Australia. We hypothesized that these frogs would be different with respect to their field hydration states because of the challenges associated with the different ecological habits. There are very few data on the hydration levels that frogs maintain in the field, and the existing data are from disparate species and locations and do not relate hydration state to habit or changes in seasonal water availability. We measured the hydration state of 15 species of frogs from tropical northern Australia to determine the influences of ecological habit and season on the hydration state that these frogs maintain. As predicted, frogs were significantly less hydrated in the dry season than they were in the wet season and showed significantly higher variation among individuals, suggesting that maintaining hydration is more challenging in the dry season. In the wet season, terrestrial species were significantly less hydrated than arboreal or amphibious species. During the dry season, amphibious species that sought refuge in cracking mud after the pond dried were significantly less hydrated than terrestrial or arboreal species. These data suggest that hydration behaviors and voluntary tolerance of dehydration vary with habitat use, even within closely related species in the same family or genus. Terrestrial and arboreal species might be expected to be the most vulnerable to changes in water availability, because they are somewhat removed from water sources, but the physiological characteristics of arboreal frogs that result in significant cutaneous resistance to water loss allow them to reduce the effects of their dehydrating microenvironment.

Amphibians are typically intolerant of high temperatures and dehydrating conditions, and small species are particularly susceptible to desiccation. The rockhole frog, Litoria meiriana (Hylidae), is diurnal and is often observed on rocks in the sun near streams in tropical Australia. These hot, desiccating conditions are avoided by most frog species.We measured the microclimate in the areas used by frogs and the activity, body temperatures and hydric state of free-ranging individuals of this small frog.We also used plaster models to further explore the dynamic nature of hydric state by combining estimates of water loss and water uptake with behavioural observations of activity and microhabitat selection. Both direct measures and estimates of dynamic hydric state indicated that free-ranging frogs generally maintained a hydric state above 95% of full hydration, but occasionally, particularly during the afternoon, frogs allowed their hydric state to fall as low as 85%. Body temperatures of frogs remained below the critical thermal maximum (CTmax) even when the frogs were in the sun, because this species has no cutaneous resistance to evaporative water loss and so they cool by evaporation. However, during the hotter part of the day, on dry sunny substrates, the hydric state of the frogs could fall to near lethal hydration states (approximately 70% of full hydration) within a short period (approximately 20 min). Thus, the threat of desiccation appears to be more limiting than the threat of overheating. These diurnal frogs rely on frequent bouts of rehydration to support their ability to venture onto hot, dry rocks during the day.

Closely related syntopic species have been shown to avoid competition by differentiating in the type of food they process. This can be achieved by changes in size or in the masticatory apparatus that produce modifications in bite force. The wood mouse (Apodemus sylvaticus (Linnaeus, 1758)) and Western Mediterranean mouse (Mus spretus Lataste, 1883) are two murid rodent species found in syntopy in the south of France. We measured bite force in wild specimens of both species to test for differences in performance. Despite its greater body mass, the wood mouse showed only slightly higher bite force than the Western Mediterranean mouse. We found no clear sexual dimorphism in either species; however, among the males of the Western Mediterranean mouse, two groups appeared in terms of bite force. This bite force difference may correspond to a hierarchical organization of these males. Overall, it seems that both species have similar bite forces and accordingly overlap in the resources they use. Other factors may exist that create a niche differentiation between the wood mouse and the Western Mediterranean mouse. Another explanation may be a great abundance of food, which would cancel competition for this resource in these species.