JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org.. Ecological Society of America is collaborating with JSTOR to digitize, preserve and extend access to Ecology.Abstract. Coexisting heteromyid rodent species of North American deserts differ in habitat use and in locomotory morphology. Quadrupedal species forage primarily in structurally complex microhabitats, such as under bush canopies, while bipedal species forage in open spaces. A common explanation for this morphology-microhabitat association is that species differing in morphology also differ in vulnerability to predators, that microhabitat structure affects predation risk, and that animals preferentially forage in the safest microhabitats. We tested this for two bipedal and two quadrupedal heteromyid species (matched by body size), and one cricetid species, by quantifying effects of habitat and illumination on activity and on risk of predation by Great Homed Owls.Capture frequencies were lower for all heteromyid species than for the cricetid species, Peromyscus maniculatus. Heteromyid activity was lower in open habitat and under bright illumination. Illumination had no significant effect on risk, perhaps because rodents changed activity patterns under full moon to compensate for a potential increment in risk. Habitat, however, did affect risk: all species were attacked and captured more frequently in the open. Bipedal species were attacked relatively more in the open than were quadrupeds. If these results apply to all predators, they indicate that predation alone cannot account for the divergent microhabitat associations of bipedal and quadrupedal species. Bipedal heteromyids, however, escaped owl attacks more frequently than did quadrupeds of equivalent size. It is therefore conceivable that they experience lower overall risk in nature, where owls may preferentially attack more easily captured prey species when given a choice. Under these circumstances, owl predation could reinforce divergent microhabitat specializations based on some other factor, such as foraging economics, by restricting quadrupeds more strongly than bipeds to the safety of bushes. Hafner 1983) in this ecologically uniform family of nocturnal, burrowing seed-eaters are found in North American deserts, where they form a dominant part of the granivore guild (Brown et al. 1979). Several heteromyid species often coexist, and one of the most conspicuous differences among species that might be important for coexistence involves habitat or microhabitat affinities (Rosenzweig and Winakur 1969, Brown and Lieberman 1973, Price 1978, Price and Brown 1983, Kotler and Brown 1988) that are correlated with locomotory morphology, a major axis of morphological variation in the family as a whole (Wood 1935). Bipedal kanga...
Natural and anthropogenic boundaries have been shown to affect population dynamics and population structure for many species with movement patterns at the landscape level. Understanding population boundaries and movement rates in the field for species that are cryptic and occur at low densities is often extremely difficult and logistically prohibitive; however genetic techniques may offer insights that have previously been unattainable. We analysed thirteen microsatellite loci for 739 mountain lions (Puma concolor) using muscle tissue samples from individuals in the Great Basin throughout Nevada and the Sierra Nevada mountain range to test the hypothesis that heterogeneous hunting pressure results in source-sink dynamics at the landscape scale. We used a combination of non-spatial and spatial model-based Bayesian clustering methods to identify genetic populations. We then used a recently developed Bayesian multilocus genotyping method to estimate asymmetrical rates of contemporary movement between those subpopulations and to identify source and sink populations. We identified two populations at the highest level of genetic structuring with a total of five subpopulations in the Great Basin of Nevada and the Sierra Nevada range. Our results suggest that source-sink dynamics occur at landscape scales for wide-ranging species, such as mountain lions, and that source populations may be those that are under relatively less hunting pressure and that occupy refugia.
Granivorous animals that cache as well as consume seeds may actually serve as mutualists to their plant resources. Seeds of Indian ricegrass (Oryzopsis hymenoides), a perennial bunchgrass in North American deserts, are consumed by various desert granivores and dispersed by seed-caching heteromyid rodents. We used a three-way factorial design at a western Nevada site to selectively exclude or allow access to experimental plots by granivorous rodents and seed harvester ants, and to subsequently follow the fate of radiolabeled Indian ricegrass seeds introduced to the plots. In addition to the presence or absence of rodents or ants, the third experimental treatment factor was to allow ''initial caching'' of the radiolabeled seeds by single Merriam's kangaroo rats (Dipodomys merriami), which were confined to certain plots for one night. Both rodents and ants larder-hoarded seeds in their burrows, but seedlings rarely established from larders. Only rodents also placed seeds in scatterhoards: shallowly buried surface caches distributed about an animal's home range. Following initial caching by a kangaroo rat, the number of seedlings established from scatterhoards was significantly greater (usually by more than an order of magnitude) than those from seeds unharvested by either type of granivore. With no initial caching, rodents reduced seedling recruitment from unharvested seeds but facilitated compensatory seedling recruitment from scatterhoards. Seeds harvested by ants seldom established seedlings. We used a seed fate model to estimate that, on average, rodents and ants harvested 96% and 7%, respectively, of seeds to which they had exclusive access, and that the probability of seedling establishment for a seed harvested by a rodent was an order of magnitude greater than from a seed harvested by an ant and slightly greater than for an unharvested seed. The predicted rank order of seedling recruitment among nine experimental treatments based on expected effects of rodent seed caching closely matched the observed ranking pattern, indicating that rodents determined seedling recruitment patterns of Indian ricegrass. Because rodents harvested such a large majority of seeds and their caches enhanced seedling establishment, they played a central role in the population dynamics of Indian ricegrass.
During 1997-1998, we investigated the influence of both the relative abundance of truffles, preferred food items, and microhabitat structure on the occurrence of northern flying squirrels (Glaucomys sabrinus Shaw) in old-growth forest habitat of the Sierra Nevada Range, U.S.A. Following live-trapping sessions, we searched the forest floor for truffle diggings and sampled the soil for truffles. Diggings were more abundant where flying squirrels were captured, suggesting squirrels were active near areas of the forest floor where truffles had recently been excavated. The frequency of sampling plots with truffles was higher where squirrels were captured, further suggesting preferences for microhabitats where truffles were more abundant. We also measured 15 microhabitat variables at trap stations to evaluate the influence of aboveground microhabitat characteristics on squirrel occurrence. Results indicated that flying squirrels preferred microhabitats with understory cover, which may minimize predation from aerial predators like spotted owls (Strix occidentalis Merriam). Neither abundance of coarse woody debris, a feature conducive to fungal growth, nor the abundance of potential nesting sites (i.e., snags) measurably influenced squirrel occurrence. While various aboveground forest-microhabitat characteristics affect the use of old-growth forests by flying squirrels, these animals refine their use of these forests based on fine-scale changes in the availability of a highly preferred and ephemeral food item.
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