Population size and trends of large carnivores are difficult to determine, but are often needed to inform conservation actions. Direct counts maintained over long time periods are extremely difficult to achieve. Indices of population sizes can be used to estimate large carnivore abundances, but are often case-, species-and sitespecific. Here, we test the general applicability of track-based indices to estimate large carnivore abundance. We surveyed 15 306.4 km of roads associated with 339 transects across a wide geographical scale, large range of densities and variable substrates for tracks of African large carnivores. A combined model for all carnivore species on sandy soils serves as a robust approach to predict large carnivore densities. Thus, indices based on track counts can provide useful estimates of carnivore abundance. We found consistent relationships between track densities and the actual carnivore densities, having taken account of substrate.

An efficient method for estimating bryophyte diversity in forest stands must consider more than just the dominant forest mesohabitat. We compared two methodologies commonly used for estimating diversity in forest ecosystems. Floristic habitat sampling (FHS) utilizes stratification of all forest mesohabitats, which includes the natural diversity of microhabitats found within and stratifies a mosaic of mesohabitats (e.g. forest, streams, seeps, and cliffs) and microhabitats (e.g. rocks logs, etc.) that are often not considered in forest research projects that use plot sampling to estimate species diversity. In Canadian cedar hemlock forest, FHS methodology recorded more than twice as many bryophyte species as plot sampling (PS). A comparison of the dominant forest mesohabitat concluded that plot sampling was not as efficient as FHS in estimating bryophyte diversity and that plot sampling can result in different interpretations of species diversity. Rare species ordination of stands sampled using FHS showed strong clustering of sites with respect to biogeoclimatic zones and age since the last major disturbance (fire or logging) as compared with rare species ordinations from PS data, which showed no delineation of stands along temporal gradients. Plot sampling has many useful applications in ecology, but floristic habitat sampling is more efficient for quantifying overall bryophyte diversity. FHS provides an excellent way to record a comprehensive list of species.

Given climate change, species' climatically suitable habitats are increasingly expected to shift poleward. Some imperilled populations towards the poleward edge of their species' range might therefore conceivably benefit from climate change. Interactions between climate and population dynamics may be complex, however, with climate exerting effects both indirectly via influence over food availability and more directly, via effects on physiology and its implications for survival and reproduction. A thorough understanding of these interactions is critical for effective conservation management. We therefore examine the relationship between climate, survival and reproduction in Canadian black-tailed prairie dogs, a threatened keystone species in an imperilled ecosystem at the northern edge of the species' range. Our analyses considered 8 years of annual mark-recapture data (2007)(2008)(2009)(2010)(2011)(2012)(2013)(2014) in relation to growing degree days, precipitation, drought status and winter severity, as well as year, sex, age and body mass. Survival was strongly influenced by the interaction of drought and body mass class, and winter temperature severity. Female reproductive status was associated with the interaction of growing degree days and growing season precipitation, with spring precipitation and with winter temperature severity. Results related to body mass suggested that climatic variables exerted their effects via regulation of food availability with potential linked effects of food quality, immunological and behavioural implications, and predation risk. Predictions of future increases in drought conditions in North America's grassland ecosystems have raised concerns for the outlook of Canadian black-tailed prairie dogs. Insights gained from the analyses, however, point to mitigating species management options targeted at decoupling the mechanisms by which climate exerts its negative influence. Our approach highlights the importance of understanding the interaction between climate and population dynamics in peripheralThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

Data paucity can seem to hinder science‐based approaches to the conservation of imperiled species. Yet, even individually limited datasets can improve understanding and management of complex ecological systems when carefully integrated. We demonstrate this approach to gain first insights on the transmission ecology of Yersinia pestis in Grasslands National Park (GNP), Canada, where both the bacterium and its rodent host, the nationally threatened black‐tailed prairie dog (BTPD, Cynomys ludovicianus), reach the northern limit of their distribution in North America. Primarily flea‐borne, Y. pestis causes sylvatic plague, a disease of exceptional relevance to both human health and wildlife conservation. We integrated data collected independently by multiple organizations in 2010–2017 across 17 BTPD colonies, where the species co‐occur with Richardson's ground squirrels (RGS, Urocitellus richardsonii). Available data included estimates of BTPD density and occupancy from visual counts and colony mapping; information on flea distribution, abundance, and prevalence of infection with Y. pestis from burrow swabbing, animal combing, and PCR assays; and the response of these variables to deltamethrin application on BTPD colony sections. Our analyses suggest that sylvatic plague in GNP is maintained at an enzootic level (i.e., chronic presence affecting a low proportion of individuals) with no evidence of widespread mortality, at least partially due to reduced flea activity after spring (percentage of prevalence in burrows: April–May = 11.69–33.89%; June–September: 1.75–3.19%), low prevalence of Y. pestis in flea samples (95% CI = 0.42–2.27%), and relatively low BTPD densities. Nonetheless, reducing flea prevalence through insecticide application had a positive effect on BTPD abundance, suggesting that enzootic plague is causing chronic mortality. Because flea prevalence on hosts was higher following drier years and higher on RGS than on BTPD (26.69% vs. 3.27%), insecticide application may be particularly important during dry periods and may need to take RGS and their movements into consideration. Differences between flea communities sampled by burrow swabbing and host combing suggest that plague surveillance should integrate both methods. Effects of projected climate change on vector life cycles, flea community composition, and host–parasite interactions warrant continued monitoring and an adaptive approach to species recovery actions and plague mitigation measures.

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