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Geology topics

Justine A. Becker

Publications and source records attributed to Justine A. Becker.

2 recordsLinked to original sources

Expression and mechanisms of behavioral plasticity in large mammals

Behavioral plasticity, the alteration of behavior in response to stimuli, is becoming increasingly important in the context of human-induced rapid environmental change. Theoretical and empirical studies suggest that the expression and magnitude of behavioral plasticity are likely facilitated or constrained primarily by two factors: environmental variation and endogenous traits such as body size. The contextual role of these factors on behavioral plasticity, however, is poorly understood; there are relatively few studies that have compared the magnitude and potential drivers of behavioral plasticity at different levels (i.e., population and individual) across species, especially in free-ranging animals with diverse behavioral traits such as large mammals. Here, we quantify and test potential hypotheses for the mechanisms underpinning behavioral plasticity at the individual and population level in response to variation in summer temperatures for 1068 animal-years in 17 populations across nine species of large mammals. All populations displayed behavioral plasticity in response to increased temperatures, modifying their relative selection for heat-relieving habitat attributes (e.g., elevation) and heat-generating behavior (i.e., movement speed). We found strong support for the hypothesis that the variability of the physical environment is an important driver of behavioral plasticity—both mean population behavioral plasticity and variation among individuals within each population in plasticity were lower with increased heterogeneity of habitat attributes such as tree cover. Yet, the variability in environmental conditions (i.e., the magnitude of the temperature increase) had no effect on behavioral plasticity within and among populations. We did not detect an effect of endogenous traits on the expression of behavioral plasticity; however, we note that data availability limited our tests of this hypothesis to a select few endogenous traits (body size, feeding guild, and sex of the tracked individuals) that predominantly vary at the species level, for which we had one to three replicate populations per species. Our results provide an integrative and generalizable understanding of the expression of behavioral plasticity among populations of large mammals in temperate environments and emphasize the important but nuanced role of environmental variation in determining the scope of behavioral plasticity in these populations.

Wyoming

How sampling design of GPS collar deployment influences consistency of mapped migration corridors over time

Federal and state agencies within the United States have recently issued directives prioritizing the conservation of ungulate migration corridors and winter ranges. The ability to identify and delineate the spatial distribution of seasonal ranges underpins these policies. While such delineations are often derived from global positioning system (GPS) collar data collected for a few years on a focal population, they are being used in long-term conservation planning. Our objectives were to quantify consistency in migration corridors from year to year and cumulatively across multiple years and identify which aspects of the sampling design of GPS collar deployment will delineate a consistent and relatively complete migration corridor. We used data from 6 sub-herds of mule deer ( Odocoileus hemionus ), a species known to have high migratory fidelity, located in Wyoming and northern New Mexico, USA, monitored for 5–7 years (510 unique individuals). We calculated 2 types of migration corridors over time: cumulative corridors where each new year of data was added to all previous years and yearly corridors where each year was based only on data collected in that year. We then calculated the year-to-year consistency in the 2 types of migration corridors by calculating the percent overlap between corridors calculated in sequential years. We found that collaring a higher proportion of a sub-herd increased the consistency in migration corridors, whereas collaring new individuals via redeployments in a subsequent year of monitoring caused corridors to shift. To obtain a corridor with ≥90% consistency (i.e., approaching the complete area used by a population in our data), our results suggest that biologists should strive to collar ≥6% of a sub-herd for a minimum of 2 years. However, if ≥6% of a sub-herd cannot be collared, monitoring for longer (3–4 years) will provide roughly 90% consistency in a migration corridor estimate for mule deer. Furthermore, adding 16–25% new individuals each year will help capture variation among individuals while maintaining corridor consistency of ≥90%, leading to a more accurate delineation of the corridor. Our results provide managers with a logistical framework for collaring projects aimed at delineating migration corridors that are durable into the future.

Colorado, New Mexico, Wyoming