Canopy Closure and Emigration by Juvenile Gopher Frogs

ABSTRACT Although studies have addressed effects of abrupt transitions in habitat type (e.g., forest-clear-cut or forest-field edges) on amphibian movements, little is known about effects of more subtle habitat transitions on patterns of migration and habitat use in amphibians. We used radiotelemetry to study movement patterns of juvenile gopher frogs (Rana capito) emigrating from ponds that were surrounded by longleaf pine (Pinus palustris) forest that varied in structure as a result of fire suppression. Our primary purpose was to determine if frogs emigrate directionally from their natal ponds and select habitat at random during their first month following metamorphosis. We found that frogs emigrated in nonrandom directions from ponds that were surrounded by heterogeneous habitat and selected fire-maintained habitat that was associated with an open canopy, few hardwood trees, small amounts of leaf litter, and large amounts of wiregrass (Aristida beyrichiana). Fire-maintained habitat contained higher densities of burrows excavated by gopher tortoises (Gopherus polyphemus) and small mammals, which are the priamry refuge sites for both juvenile and adult gopher frogs. Frogs moved up to 691 m from their natal ponds, frequently crossed dirt roads, and even seemed to use these roads as migration corridors. To maintain suitable terrestrial habitat for gopher frogs, including habitat used by migrating individuals, it is important to apply frequent prescribed fire to uplands surrounding breeding ponds that lead all the way to the edges of breeding ponds, as well as through ponds during periodic droughts.     

The influence of hydrostatic pressure and urethane on the thermal inactivation of bacteriophage

In Difco nutrient broth, containing 0.5 per cent NaCl, pH 6.6, Escherichia coli phages T1, T2, and T5 were inactivated at 66 degrees C., and T7 at 60 degrees C., at nearly the same rate. In each case the rate of destruction was not uniform but more or less decreased with time of heating. With T2 there was an initial increase in number of infective centers after heating for several minutes at 66 degrees C. Hydrostatic pressures up to 10,000 pounds per square inch retarded the thermal destruction of T1, T2, and T5, but accelerated that of T7, while small concentrations of urethane accelerated the rate of each. The rate of inactivation was increased by the addition of 0.005 M phosphate, and was decreased by 0.005 M MgCl(2) in all but T7, whose rate was unaffected by this amount of Mg. The influence of Ca was similar to that of Mg. The addition of 0.005 M MgCl(2) to the broth medium resulted in a first order rate of destruction of T5 at either normal or increased pressure, and with as well as without urethane. Analysis of data obtained under these conditions indicated that the thermal inactivation proceeds with a volume increase of activation of 113 cc. per mol, and with a heat and entropy of 170,000 calories and 425 E. U., respectively, in the rate-limiting reaction. In the presence of 0.1 M urethane the heat and volume change of activation are apparently slightly greater. The relation between concentration of urethane and the amount of acceleration in rate of destruction at normal pressure and 66 degrees C. indicated that the total rate involves at least two first order rate processes: the thermal inactivation itself and a urethane-catalyzed reaction, the latter involving the combination of an average of 2.3 molecules of urethane in the activated state of the bacteriophage molecule whose destruction results in loss of phage activity.