Herbivory by domestic and wild ungulates is a major driver of global vegetation dynamics. However, grazing is not considered in dynamic global vegetation models, or more generally in studies of the effects of environmental change on ecosystems at regional to global scale. An obstacle to this is a lack of empirical tests of several hypotheses linking plant traits with grazing. We, therefore, set out to test whether some widely recognized trait responses to grazing are consistent at the global level. We conducted a meta-analysis of plant trait responses to grazing, based on 197 studies from all major regions of the world, and using six major conceptual models of trait response to grazing as a framework. Data were available for seven plant traits: life history, canopy height, habit, architecture, growth form (forb, graminoid, herbaceous legume, woody), palatability, and geographic origin. Covariates were precipitation and evolutionary history of herbivory. Overall, grazing favoured annual over perennial plants, short plants over tall plants, prostrate over erect plants, and stoloniferous and rosette architecture over tussock architecture. There was no consistent effect of grazing on growth form. Some response patterns were modified by particular combinations of precipitation and history of herbivory. Climatic and historical contexts are therefore essential for understanding plant trait responses to grazing. Our study identifies some key traits to be incorporated into plant functional classifications for the explicit consideration of grazing into global vegetation models used in global change research. Importantly, our results suggest that plant functional type classifications and response rules need to be specific to regions with different climate and herbivory history.

This work shows the applicability of a set of protocols that can be widely applied to assess the impacts of global change drivers on species, communities and ecosystems.

The spatial distribution of woody plants was studied in an arid savanna in Botswana. The study included stands of mixed species and sizes as well as monospecific even‐sized stands of different size classes of the tree Acacia erioloba and the shrub Acacia mellifera. In the case of A. mellifera both dense stands on overgrazed land and more open stands were included. The analysis used all plant‐to‐plant distances, and individuals were represented with a realistic canopy extension. The mixed stands showed aggregated distribution of individuals, mainly caused by strong clumping of small shrubs. In A. erioloba saplings were aggregated, small trees were randomly or regularly distributed and large trees were randomly spaced. In open stands of A. mellifera aggregation increased with size of the shrubs, while in dense stands with overgrazing aggregation decreased with increasing size. The different patterns are discussed in relation to the relative importance of inter‐ and intraspecific competition for water and of disturbance by fire as regulatory mechanisms for total amount and spatial distribution of woody plants in this savanna.

Habitat alteration by humans may change the supply of food and cover for wild ungulates, but few studies have examined how these resources are utilised over time by individuals of different sex and reproductive status. We examined circadian and seasonal variation in habitat utilisation within a moose Alces alces population in central Norway. Our study area covers forests and open habitats, both influenced by human alterations (e.g. forestry and agriculture). We expected moose to select habitats with good forage and cover in all seasons, but to select open foraging habitats mainly during night-time. Moose selected good foraging habitats, such as young forest stands and cultivated land during night, whereas the utilisation of older forest stands providing cover increased during daytime. This circadian pattern changed throughout the year, seemingly related to variation in hours of daylight and provision of forage. Young forest stands provided higher density of preferred food plants compared to older stands and were highly selected from spring until autumn. Relative to young forest, the selection for older forest stands increased towards winter, likely due to provision of higher plant quality late in the growing season, and to reduced accumulation of movement-impeding snow during winter. Selection of cultivated land varied among seasons, being highest when crop biomass was high. We also found some indications of state-dependent habitat selection as reproducing females avoided open, food rich areas in the first months after their calves were born, whereas males and females without young selected these areas in spring and summer. Our results clearly show that moose exploit the variations in cover and food caused by forestry and agriculture. This is particularly relevant for moose in Norway as current changes in forestry practice lead to a reduction in young, food-rich forest stands, possibly aggravating the already declining body conditions and recruitment rates of moose.

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