| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Population impacts of movements of individuals | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Previously, we had considered how growth, survival, and behavioral preferences of individuals affected population dynamics, but it became clear in these studies that movement is also an individual response that must be incorporated. Much of our recent and current work continues to focus on understanding population and community consequences of individual behaviors and vital rates, but with an emphasis on individual movements and their implications. | Dr. Elizabeth Marschall Home page | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
The cost of dispersal: predation as a function of movement and site familiarity in ruffed grouse] Ecologists often assume that dispersing individuals experience increased predation risk owing to increased exposure to predators while moving. To test the hypothesis that predation risk is a function of movement distance or rate of movement, we used radio-telemetry data collected from 193 ruffed grouse (Bonasa umbellus) during 19961999 in southeastern Ohio. Cox's proportional hazards model was used to examine whether the risk of predation was affected by the rate of movement and site familiarity. We found evidence indicating that increased movement rates may increase the risk of predation for adult birds but not juveniles. We also found juvenile and adult birds inhabiting unfamiliar space were consistently at a much higher risk of predation (three to 7.5 times greater) than those in familiar space. Our results indicate that although movement itself may have some effect on the risk of being preyed upon, moving through unfamiliar space has a much greater effect on risk for ruffed grouse. This supports the hypothesis that increased predation risk may be an important cost of dispersal for birds.
Understanding movement and spatial structure of Lake Erie fish populations
Movement of reservoir-stocked riverine fish between tailwaters, streams, and rivers We first characterized the timing and direction of movement of stocked saugeye (hatchery produced walleye x saugeye hybrid) from Ohio reservoirs so that we could begin to understand the potential for undesirable side effects, such as genetic mixing with downstream parental stocks and ecological impacts on native stream communities. We designed the study to address the conventional wisdom that small fish are susceptible to being flushed from reservoirs during high discharge and that adult saugeye exhibit seasonal directional movement patterns similar to those exhibited by its parent species, walleye and sauger. Contrary to our initial expectations, (1) saugeye tailwater abundance was unrelated to reservoir discharge, (2) first-summer saugeye survival was highest in reservoirs with fast turnover (i.e., high discharges), (3) small saugeye were less likely to move downstream than larger ones, and (4) soon after stocking, YOY saugeye moved both up- and downstream from reservoirs, in some cases moving upstream some 50 km during high discharges. In our view, much of conventional wisdom suggesting that discharge drives saugeye abundance in tailwaters and negatively affects within-reservoir survival through direct losses of YOY can be explained by seasonal hydrographs that happen to coincide with behavioral cues (i.e., temperature, photoperiod, etc.) rather than by reservoir discharge per se.
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||