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Geology topics

Mark A. Thonhoff

Publications and source records attributed to Mark A. Thonhoff.

2 recordsLinked to original sources

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

Short-term responses to a human-altered landscape do not affect fat dynamics of a migratory ungulate

According to risk-sensitive foraging theory, animals should make foraging decisions that balance nutritional costs and gains to promote fitness. Human disturbance is a form of perceived risk that can prompt avoidance of risky habitat over acquisition of food. Consequently, behavioural responses to perceived risk could induce nutritional costs. Population declines often coincide with increases in human disturbance, which likely is associated with direct and indirect habitat loss. Nevertheless, behavioural and physiological responses to perceived risks associated with human disturbance could be an added nutritional deficit with population-level repercussions. Using GPS-collar data from three populations of migratory mule deer Odocoileus hemionus exposed to a gradient of established industrial energy development on winter ranges where direct and indirect habitat loss were well documented, we evaluated whether exposure and behavioural responses to human disturbance alter changes in nutritional condition (i.e. fat reserves) over winter. Although animals exhibited behaviours indicative of perceived risk of human disturbance, such as increased movement rates and avoidance of infrastructure, exposure and behavioural responses to human disturbance had little to no measurable effect on fat loss over a winter. Instead, catabolism of fat reserves occurred primarily as a function of the amount of fat animals had entering winter, suggesting that, in the short term, animals were able to mitigate the energetic costs of perceived risk of human disturbance over winter. Animals, however, did not appear to overcome persistent food limitations, and animals with less food availability lost more fat over winter. Our findings heed caution in using short-term behavioural and physiological responses to inform long-term nutritional consequences of human disturbance. Although animals appear to mitigate the energetic costs of perceived risk, food limitations exacerbated by broader-scale avoidance of food near human disturbance may be the primary pathway causing the frequently observed population declines following human disturbance to pristine landscapes.

Wyoming