Amphibian biology and husbandry.

Extant amphibians comprise three lineages-- salamanders (Urodela or Caudata), frogs and toads (Anura), and caecilians (Gymnophiona, Apoda, or Caecilia)--which contain more than 6,000 species. Fewer than a dozen species of amphibians are commonly maintained in laboratory colonies, and the husbandry requirements for the vast majority of amphibians are poorly known. For these species, a review of basic characteristics of amphibian biology supplemented by inferences drawn from the morphological and physiological characteristics of the species in question provides a basis for decisions about housing and feeding. Amphibians are ectotherms, and their skin is permeable to water, ions, and respiratory gases. Most species are secretive and, in many cases, nocturnal. The essential characteristics of their environment include appropriate levels of humidity, temperature, and lighting as well as retreat sites. Terrestrial and arboreal species require moist substrates, water dishes, and high relative humidity. Because temperature requirements for most species are poorly known, it is advisable to use a temperature mosaic that will allow an animal to find an appropriate temperature within its cage. Photoperiod may affect physiology and behavior (especially reproduction and hibernation), and although the importance of ultraviolet light for calcium metabolism by amphibians is not yet known, ecological observations suggest that it might be important for some species of frogs. Some amphibians are territorial, and some use olfactory cues to mark their territory and to recognize other individuals of their species. All amphibians are carnivorous as adults, and the feeding response of many species is elicited by the movement of prey. Diets should include a mixture of prey species, and it may be advisable to load prey with vitamins and minerals.

Effects of body temperature and hydration state on organismal performance of toads, Bufo americanus.

Temperature and humidity are dominant environmental variables affecting performance of nocturnal, terrestrial amphibians. Toads are frequently active at body temperatures (T(b)) and hydration states (HS) that yield suboptimal performance. We investigated the combined effects of T(b) and HS on feeding, locomotion, and metabolism of Bufo americanus. More toads responded to the presence of prey when fully hydrated than when dehydrated, and times to orient to prey, maneuver around a barrier, and reach prey were less in hydrated than in dehydrated animals. Time to capture prey decreased with increasing T(b) in fully hydrated, but not dehydrated, toads, and hydrated animals caught prey more rapidly than did dehydrated animals. Distance traveled in 5 min and aerobic scope were affected by T(b). Generally, individuals that performed well in the feeding experiments at a particular T(b) and HS also performed well at a different T(b) and HS. The same was true for distance traveled and aerobic scope. However, within combinations of T(b) and HS, correlations between performance variables were minimal. Specialization of a particular variable resulting in high performance at a certain T(b) and HS does not appear to exact a cost in terms of performance at a different T(b) and HS.

Prey-handling and the evolutionary ecology of sand-swimming lizards (Lerista : Scincidae).

Fossorial lizards differ in morphology from their surface-dwelling relatives. The Australian sphenomorphine skink genus Ctenotus consists of surface-dwelling species, and is closely related to the genus Lerista, which includes both surface-dwelling and fossorial species. Sand-swimming represents the derived condition and has evolved independently in several lineages of Lerista. The heads of lizards in the two genera differ in shape (blunt snout for Ctenotus versus wedge-shaped for Lerista) and in length relative to the body (approximately 20% of snout-vent length for Ctenotus versus 12% for sand-swimming Lerista). Do these specializations affect the sizes or types of prey that can be consumed by Lerista? We compared prey-handling by Ctenotus and Lerista to correlate morphological differences with differences in prey-handling ability, and to distinguish the effects of snout shape and head length. Feeding trials included three categories of insect prey that the lizards normally eat: soft-bodied larvae (Lepidoptera), hard-bodied larvae (Coleoptera), and roaches (Blatoidea). In comparisons based on the mass of a prey item relative to the mass of a lizard, Lerista had longer handling times for all prey categories and were limited to smaller prey than were Ctenotus. However, when comparisons were based on the length of prey relative to the length of a lizard's head, Lerista ate some elongate prey as fast or faster than did Ctenotus, and both genera successfully swallowed prey more than twice the length of their own head. Thus, the differences in prey-handling performance of Ctenotus and Lerista probably result from the fact that Lerista have a relatively shorter head than Ctenotus. All Lerista species, surface-dwelling and fossorial, have short heads compared to primitive sphenomorphine lizards. Fossorial species of Lerista have elongate trunks, and consequently their heads are shorter in proportion to trunk length than those of surface-dwelling Lerista. However, most fossorial species of Lerista are longer and heavier than any of their surface-dwelling congeners, and the heads of these fossorial species are large relative to the prey they encounter. As a consequence, the diets of large fossorial species of Lerista do not appear to be limited by their morphological specialization for sand-swimming.

Post-metamorphic change in activity metabolism of anurans in relation to life history.

Newly-metamorphosed individuals of some species of frogs and toads differ from adults in behavior, ecology, and physiology. These differences may be related to broader patterns of the life histories of different species of frogs. In particular, the length of larval life and the size of a frog at metamorphosis appear to be significant factors in post-metamorphic ontogenetic change. These changes in performance are associated with rapid post-metamorphic increases in oxygen transport capacity. Bufo americanus (American toads) and Rana sylvatica (wood frogs) spend only 2-3 months as tadpoles and metamorphose at body masses of 0.25 g or less. Individuals of these species improve endurance and aerobic capacity rapidly during the predispersal period immediately following metamorphosis. Increases in hematocrit, hemoglobin concentration, and heart mass relative to body mass are associated with this improvement in organismal performance. Rana clamitans (green frogs) spend from 3 to 10 months as larvae and weigh 3 g at metamorphosis. Green frogs did not show immediate post-metamorphic increases in performance. Rana palustris (pickerel frogs) are intermediate to wood frogs and green frogs in length of larval life and in size at metamorphosis, and they are intermediate also in their post-metamorphic physiological changes.American toads and wood frogs appear to delay dispersal from their natal ponds while they undergo rapid post-metamorphic growth and development, whereas green frogs disperse as soon as they leave the water, even before they have fully absorbed their tails. The very small body sizes of newly metamorphosed toads and wood frogs appear to limit the scope of their behaviors. The brief larval periods of these species permit them to exploit transient aquatic habitats, but impose costs in the form of a period of post-metamorphic life in which their activities are restricted in time and space compared to those of adults.

Ecological correlates of anuran exercise physiology.

Studies of exercise physiology of anuran amphibians have led to the suggestion that there is a dichotomy between species that depend upon movement to escape from predators and species that utilize static defenses. This generalization has been based upon a limited taxonomic survey and it contrasts with morphological, ecological, and behavioral studies that have revealed diverse and complex interrelationships among these features of anuran biology. We tested the hypothesis of a dichotomy of physiological types among anurans by measuring aerobic and anaerobic metabolism during maximum exercise for 17 species representing seven families and a variety of ecological types and locomotor modes. All degrees of dependence upon aerobic and anaerobic power input were found among the 17 species and the variation did not follow phylogenetic divisions. No single, simple prediction of the predominant source of power utilized for activity by the anurans we studied is possible. Predator avoidance behavior was not significantly correlated with the metabolic pattern. Predatory mode (active versus passive searchers) and mode of locomotion (non-jumpers versus jumpers) were correlated with dependence upon aerobic energy production and with each other. Reproductive behavior is probably another associated factor. The diversity of modes of power input among anurans is great and is intimately linked with numerous features of a species' biology. Single-factor explanations of this physiological characteristic are not appropriate.

Physiological basis of habitat partitioning in Jamaican Eleutherodactylus.

Rate of evaporation, resistance to drying, temperature selection, and critical thermal maximum were measured for Jamaican Eleutherodactylus acclimated to 20° C and a 12:12 L:D photoperiod. Two introduced species, E. planirostris and E. johnstonei, selected higher temperatures and had higher CTMs than two native species, E. cundalli and E. gossei. The introduced species lost water as rapidly as the native species, but tolerated 30-73% greater water loss before losing their righting response. The physiological differences are reflected in the microhabitat selection and activity patterns of the four species.