Shifts in microbial populations of the intestinal tract have been associated with a multitude of nutritional, autoimmune, and infectious diseases. The limited diversity following antibiotic treatments creates a window for opportunistic pathogens, diarrhea, and inflammation as the microbiome repopulates. Depending on the antibiotics used, microbial diversity can take weeks to months to recover. To alleviate this loss of diversity in the intestinal microbiota, supplementation with probiotics has become increasingly popular. However, our understanding of the purported health benefits of these probiotic bacteria and their ability to shape the microbiome is significantly lacking. This study examined the impact of probiotics concurrent with antibiotic treatment or during the recovery phase following antibiotic treatment of mice. We found that probiotics did not appear to colonize the intestine themselves or shift the overall diversity of the intestinal microbiota. However, the probiotic supplementation did significantly change the types of bacteria which were present. In particular, during the recovery phase the probiotic caused a suppression of Enterobacteriaceae outgrowth (Shigella and Escherichia) while promoting a blooming of Firmicutes, particularly from the Anaerotruncus genus. These results indicate that probiotics have a significant capacity to remodel the microbiome of an individual recovering from antibiotic therapy.

The roles of dispersal and population dynamics in determining species' range boundaries recently have received theoretical attention but little empirical work. Here we provide data on survival, reproduction, and movement for a Virginia opossum (Didelphis virginiana) population at a local distributional edge in central Massachusetts (USA). Most juvenile females that apparently exploited anthropogenic resources survived their first winter, whereas those using adjacent natural resources died of starvation. In spring, adult females recolonized natural areas. A life-table model suggests that a population exploiting anthropogenic resources may grow, acting as source to a geographically interlaced sink of opossums using only natural resources, and also providing emigrants for further range expansion to new human-dominated landscapes. In a geographical model, this source-sink dynamic is consistent with the local distribution identified through road-kill surveys. The Virginia opossum's exploitation of human resources likely ameliorates energetically restrictive winters and may explain both their local distribution and their northward expansion in unsuitable natural climatic regimes. Landscape heterogeneity, such as created by urbanization, may result in source-sink dynamics at highly localized scales. Differential fitness and individual dispersal movements within local populations are key to generating regional distributions, and thus species ranges, that exceed expectations.

While climatic limitations are widely recognized as primary factors determining the distributions of many species, the physiological link between climate and species’ persistence is poorly understood. The Virginia opossum Didelphis virginiana is a species for which winter energetics have been evaluated and a northern geographical limit has been hypothesized. Expansion of opossum populations beyond this limit, however, suggests that a previous winter energetics model requires modification. I update this energetics model by incorporating random foraging success to estimate the probability of opossum survival under varying winter temperature regimes. Estimation of opossum “success” for winters in Amherst, Massachusetts, since 1926 showed that juvenile females, the key breeding component of the population, would survive at a rate high enough to maintain a stable population in only 4 of the 77 yr. The model correctly predicted the fate of 13 of 14 opossums monitored in the Amherst area during the winters of 2000–2003. The current energetics model does not correctly predict autumn weight gain, but it does accurately estimate opossum winter survival. However, the model predicts that opossums should be winter‐limited in areas such as Amherst, Massachusetts, where in fact they are well established. This discrepancy may be explained in three ways: weather station data do not adequately reflect available microclimates, opossums show high levels of flexibility in cold‐weather foraging behavior, and most likely, humans provide food and shelter that mitigate the effect of winter.

Individual personality is an important source of variation in animal behavior. However, few studies have examined the reliability of individual behaviors across both time and context for even common temperament traits such as boldness, especially in mammals. We tested a laboratory colony of Siberian dwarf hamsters (Phodopus sungorus) in two similar assays, a tunnel maze and an open field, both provisioned with a home nestbox for shelter. Animals were tested in each assay at three ages, beginning at weaning. Principal components analysis on each assay identified an axis of activity level in both tests, boldness and reactivity in the tunnel maze, and nestbox orientation in the open field. All traits were moderately (7–18%) heritable. Individual activity level was the most reliably consistent trait, both within and between tests. Tunnel maze boldness, tunnel maze reactivity, and open field nestbox orientation did not correlate at any age. Correlation between boldness and activity changes from positive to negative as animals age, while reactivity was consistently negatively associated with activity. A negative correlation emerged in adults between open field activity and nestbox orientation. These results suggest that either development or habituation results in different personality trait associations in an individual over time. Individual temperament traits such as general activity level may be quite stable, but caution should be used in generalizing single assays to represent boldness across time and across contexts.