Total evaporative water loss is the sum of respiratory water loss (RWL) and cutaneous water loss (CWL) and constitutes the main avenue of water loss in bats. Because bats fly and have large surface-to-volume ratios, they potentially have high rates of RWL and CWL. Most species of small insectivorous bats have the ability to reduce their body temperature (T(b)) at rest, which substantially reduces energy expenditure and water loss. We hypothesized that bats reduce evaporative water loss during bouts of deep hypothermia (torpor) by decreasing RWL and CWL. We measured T(b), RWL, CWL, and resting metabolic rate (RMR) in Kuhl's pipistrelle Pipistrellus kuhlii, a small insectivorous bat. In support of our hypothesis, we found that RWL decreased with decreasing RMR. We found that CWL was lower in torpid individuals than in normothermic bats; however, bats in deep torpor had similar or higher CWL than bats in shallow torpor, suggesting that they exert a less effective physiological control over CWL when in deep torpor. Because insectivorous bats spend most of their lives in torpor or hibernation, the regulation of CWL in different heterothermic states has relevant ecological and evolutionary consequences.

The water vapour permeability barrier of mammals and birds resides in the stratum corneum (SC), the outermost layer of the epidermis. The molar ratio and molecular arrangement of lipid classes in the SC determine the integrity of this barrier. Increased chain length and polarity of ceramides, the most abundant lipid class in mammalian SC, contribute to tighter packing and thus to reduced cutaneous evaporative water loss (CEWL). However, tighter lipid packing also causes low SC hydration, making it brittle, whereas high hydration softens the skin at the cost of increasing CEWL. Cerebrosides are not present in the mammalian SC; their pathological accumulation occurs in Gaucher's disease, which leads to a dramatic increase in CEWL. However, cerebrosides occur normally in the SC of birds. We tested the hypothesis that cerebrosides are also present in the SC of bats, because they are probably necessary to confer pliability to the skin, a quality needed for flight. We examined the SC lipid composition of four sympatric bat species and found that, as in birds, their SC has substantial cerebroside contents, not associated with a pathological state, indicating convergent evolution between bats and birds.

Burrows are animal-built structures that can buffer their occupants against the vagaries of the weather and provide protection from predators. We investigated whether the trapdoors of wolf spider (Lycosa sp.; temporary working name "L. hyraculus") burrows in the Negev Desert serve to maintain favorable environmental conditions within the burrow by removing trapdoors and monitoring the ensuing temperature and relative humidity regime within them. We also monitored the behavioral responses of “L. hyraculus” to trapdoor removal at different times of the day and in different seasons. “L. hyraculus” often spun silk mesh in their burrow entrances in response to trapdoor removal during the day, possibly to deter diurnal predators. The frequency of web-spinning peaked on summer mornings, but spiders began spinning webs sooner after trapdoor removal later in the day. In addition, we monitored temperature and relative humidity in artificial burrows in the summer during the morning and at midday. At noon, air temperature (T_a) at the bottom of open burrows increased by <1 °C more than in covered burrows, but water vapor pressure in burrows did not change. The relatively small increase in T_a in uncovered burrows at midday can probably be ascribed to the penetration of direct solar radiation. Thus, air temperature and humidity at the bottom of the burrow are apparently decoupled from airflow at the surface.

Nidicolous ectoparasites such as fleas and gamasid mites that feed on small and medium-sized mammals spend much of their time in their hosts' burrows, which provide an environment for living, and often feeding, to their pre-imaginal and/or adult stages. Thus, these ectoparasites should be adapted to environmental conditions in burrows, including high fractional concentrations of CO₂ (FCO₂). We examined how a high FCO₂ (0.04) affected survival and reproductive success of a hematophagous ectoparasite of burrowing rodents using fleas Xenopsylla ramesis and Sundevall's jirds Meriones crassus. In the first experiment, fleas fed on hosts housed in high-CO₂ (FCO₂=0.04) or atmospheric-CO₂ (FCO₂≈0.0004) air, and were allowed to breed. In a second experiment, fleas were maintained in high CO₂ or CO₂-free air with no hosts to determine how CO₂ levels affect survival and activity levels. We found that at high FCO₂ fleas laid fewer eggs, reducing reproductive success. In addition, at high FCO₂, activity levels and survival of fleas were reduced. Our results indicate that fleas do not perform well in the FCO₂ used in this experiment. Previous research indicated that the type and intensity of the effects of CO₂ concentration on the fitness of an insect depend on the FCO₂ used, so we advise caution when generalizing inferences drawn to insects exposed to other FCO₂. If, however, FCO₂ found in natural mammal burrows brings about reduced fitness in fleas in general, then burrowing hosts may benefit from reduced parasite infestation if burrow air FCO₂ is high.

We studied the influence of manipulating predation risk on Allenby’s gerbil ( Gerbillus andersoni allenbyi) held in a large, outdoor enclosure. We measured giving up densities (GUDs), apprehension, time allocation to foraging, harvest strategy (grab and go (GAG) vs. eat at tray (EAT)), and fecal cortisol concentration. First we established the time necessary for cortisol and corticosterone concentrations to change significantly from baseline after a stressful experience. To do this we collected feces from gerbils 2, 4, 6, or 8 hours after being handled (treatment) or not (control). After 8 h, fecal cortisol, but not corticosterone, concentration was significantly higher in treatment animals. We used the results from the hormone time course experiment to design the predation experiment. We used a dog, trained to harass gerbils, to increase predation risk for the gerbils. We predicted that fecal cortisol concentrations would increase directly in the face of predation risk, or indirectly, due to reduced foraging time because of perceived predation risk that, in turn, leads to increased hunger levels. As predicted, in the presence of a predator, GUDs were higher, time allocation lower, and GAG foraging was used more in treatment animals than in controls, but we found no change in apprehension. There was no difference in cortisol concentration between predator present and no-predator treatments. However, individuals that tended to have higher average fecal cortisol concentrations also tended, on average, to spend more time foraging. This indicates a relationship between stress hormones and optimal foraging. This relationship is potentially causal. While nightly changes in behavior may not be related to stress hormones, over course time scales, stress hormones may be driving gerbils to forage more.