Impact of predation risk on emergence by little brown bats, Myotis lucifugus (Chiroptera: Vespertilionidae), from a maternity colony.

When bats emerge from their roosts in the evening to forage and drink, it appears as though their departure involves brief periods when many individuals emerge interspersed with periods during which few individuals emerge. Clustering is seen in many species of animals and probably has an anti-predator or information-transfer function. Regardless of its function, clustering in the emergence of bats may intensify as a result of large numbers of individuals trying to pass through a small exit hole in a short period of time. A total of 31 observations of emergence were made from May to Aug. 1992 and 1993 at a maternity colony of little brown bats (Myotis lucifugus), in Cypress Hills, Saskatchewan, Canada. To determine the effects of a predator on clustering in the emergence, a plastic great horned owl (Bubo virginianus) was used as a predator model and mounted close to roost exits on 8 nights. Recorded calls of a great horned owl were played back towards the roost. The predator model and associated calls did not affect the number of bats that emerged, the median time of emergence, or the degree of clustering in the emergence. There was a significant positive relationship between the extent of clustering in the emergence and the number of bats that emerged. Emergences of more than 25 bats were clustered. Thus, we found no evidence to support clustering during emergence as being an anti-predator response. However, clustering may be intensified with increased numbers of individuals trying to pass through a narrow space in a short period of time

Food Habits of Rodents Inhabiting Arid and Semi-arid Ecosystems of Central New Mexico

In this study, we describe seasonal dietary composition for 15 species of rodents collected in all major habitats on the Sevilleta National Wildlife Refuge (Socorro County) in central New Mexico. A comprehensive literature review of food habits for these species from throughout their distribution also is provided. We collected rodents in the field during winter, spring and late summer in 1998 from six communities: riparian cottonwood forest; piñon-juniper woodland; juniper-oak savanna; mesquite savanna; short-grass steppe; and Chihuahuan Desert scrubland. Rodents included Spermophilus spilosoma (Spotted Ground Squirrel), Perognathus flavescens (Plains Pocket Mouse), Perognathus flavus (Silky Pocket Mouse), Dipodomys merriami (Merriams Kangaroo Rat), Dipodomys ordii (Ord\u27s Kangaroo Rat), Dipodomys spectabilis (Banner-tailed Kangaroo Rat), Reithrodontomys megalotis (Western Harvest Mouse), Peromyscus boylii (Brush Mouse), Peromyscus eremicus (Cactus Mouse), Peromyscus leucopus (White-footed Mouse), Peromyscus truei (Piñon Mouse), Onychomys arenicola (Mearn\u27s Grasshopper Mouse), Onychomys leucogaster (Northern Grasshopper Mouse), Neotoma albigula/leucodon (White-throated Woodrats), and Neotoma micropus (Southern Plains Woodrat). We collected stomach contents of all species, and cheek-pouch contents of heteromyids, and quantified them in the laboratory. We determined seasonal diets in each habitat by calculating mean percentage volumes of seeds, arthropods and green vegetation (plant leaves and stems) for each species of rodent. Seeds consumed by each rodent were identified to genus, and often species, and quantified by frequency counts. Comparisons of diets between and among species of rodents, seasons, and ecosystems were also examined. We provide an appendix of all plant taxa documented.\u2