Summary 1.Competitor, stress-tolerator, ruderal (CSR) theory is a prominent plant functional strategy scheme previously applied to local floras. Globally, the wide geographic and phylogenetic coverage of available values of leaf area (LA), leaf dry matter content (LDMC) and specific leaf area (SLA) (representing, respectively, interspecific variation in plant size and conservative vs. acquisitive resource economics) promises the general application of CSR strategies across biomes, including the tropical forests hosting a large proportion of Earth's diversity. 2. We used trait variation for 3068 tracheophytes (representing 198 families, six continents and 14 biomes) to create a globally calibrated CSR strategy calculator tool and investigate strategy-environment relationships across biomes world-wide. 3. Due to disparity in trait availability globally, co-inertia analysis was used to check correspondence between a 'wide geographic coverage, few traits' data set and a 'restricted coverage, many traits' subset of 371 species for which 14 whole-plant, flowering, seed and leaf traits (including leaf nitrogen content) were available. CSR strategy/environment relationships within biomes were investigated using fourth-corner and RLQ analyses to determine strategy/climate specializations. 4. Strong, significant concordance (RV = 0Á597; P < 0Á0001) was evident between the 14 trait multivariate space and when only LA, LDMC and SLA were used. 5. Biomes such as tropical moist broadleaf forests exhibited strategy convergence (i.e. clustered around a CS/CSR median; C:S:R = 43:42:15%), with CS-selection associated with warm, stable situations (lesser temperature seasonality), with greater annual precipitation and potential evapotranspiration. Other biomes were characterized by strategy divergence: for example, deserts varied between xeromorphic perennials such as Larrea divaricata, classified as S-selected (C:S:R = 1:99:0%) and broadly R-selected annual herbs (e.g. Claytonia perfoliata; R/CR-selected; C:S:R = 21:0:79%). Strategy convergence was evident for several growth habits (e.g. trees) but not others (forbs). 6. The CSR strategies of vascular plants can now be compared quantitatively within and between biomes at the global scale. Through known linkages between underlying leaf traits and growth rates, herbivory and decomposition rates, this method and the strategy-environment relationships it elucidates will help to predict which kinds of species may assemble in response to changes in biogeochemical cycles, climate and land use.

International audienceno abstrac

International audienceWe expand the concept of “old growth” to encompass the distinct ecologies and conservation values of the world's ancient grass-dominated biomes. Biologically rich grasslands, savannas, and open-canopy woodlands suffer from an image problem among scientists, policy makers, land managers, and the general public, that fosters alarming rates of ecosystem destruction and degradation. These biomes have for too long been misrepresented as the result of deforestation followed by arrested succession. We now know that grassy biomes originated millions of years ago, long before humans began deforesting. We present a consensus view from diverse geographic regions on the ecological characteristics needed to identify old-growth grasslands and to distinguish them from recently formed anthropogenic vegetation. If widely adopted, the old-growth grassland concept has the potential to improve scientific understanding, conservation policies, and ecosystem management

No abstract

No abstract

The classification of plant species according to the CSR ecological strategy scheme has been proposed as a common language that allows comparison among species, communities and floras.Although several studies on European continent have demonstrated a consistent association between CSR strategies and key ecosystem processes, studies of this type are still lacking in other ecoregions worldwide. For the first time the CSR strategy scheme is applied in a tropical plant community. In a Brazilian mountain grassland ecosystem characterized by both high biodiversity and environmental stress, we sampled various functional traits of 48 herbaceous species in stony and sandy grasslands, and evaluated the relationship between CSR strategies and functional traits with several environmental parameters. The extremely infertile soils in the two studied habitats may have acted as a major environmental filter leading to a clear predominance of the stress-tolerant strategy in both communities. However, fine-scale environmental differences between the two communities resulted in the filtering of distinct functional trait values. The sites with coarser soil texture, lower percentage of plant cover and (paradoxically) higher mineral nutrient concentrations favored plants with narrower leaves, higher stress tolerance, lower competitiveness, and higher sclerophylly (i.e., lower specific leaf area and higher leaf dry matter content). The comparison between the functional character of stony and sandy communities evidenced the influence of soil texture and water availability in the environmental filtering. This study highlighted the validity of the CSR classification outside the temperate region where it was originally developed and corroborated.

Ontogenetic shifts in plants are ubiquitous, but their ecological and evolutionary significance remain largely unknown. Juveniles have few opportunities to accumulate sufficient biomass to withstand damage, whereas adults allocate resources to reproduction. Thus, age‐specific environmental filters are expected to drive selection towards specific resource‐investment strategies for each developmental stage. We tested whether species exhibited strategies that favour faster rates of biomass accumulation during early developmental stages to cope with vulnerability, shifting towards habitat‐dependent strategies to optimise resource acquisition and use later on. We also hypothesised that juveniles exhibit greater intraspecific variability of strategies than adults, as a result of continuous filtering of traits throughout the plant’s development towards adulthood. We measured key leaf traits—leaf area (LA), leaf dry matter content (LDMC) and specific leaf area (SLA)—and calculated scores for competitor (C), stress‐tolerator (S), ruderal (R) strategies of the CSR system for juveniles of 54 species and conspecific adults of 27 species naturally occurring either in unproductive (grassland) or productive (forest) habitats. Juveniles exhibited higher SLA and LA and lower LDMC, and thus a more R‐strategy in both habitats when compared with adults, but were not necessarily “R” in absolute terms. We also found smaller intraspecific variation for the R‐strategy in adults compared with juveniles in both habitats, whereas the variation of the other strategies was habitat dependent. Ontogenetic shifts in ecological strategies appear to have been selected as a response to ontogeny‐dependent filters. Thus, strategies that favour less costly leaves and faster growth rates (relatively R‐selected) in juveniles shift towards C and/or S strategies in adulthood, depending on habitat productivity. Nevertheless, habitat‐dependent specialisation seems to be a major driver of ecological strategy selection in juveniles. Our study reveals ontogeny‐dependent strategies, offering a new approach to integrate plant development and functional specialisation. A http://onlinelibrary.wiley.com/doi/10.1111/1365-2435.13221/suppinfo is available for this article.

Our results support the view that long-term climatic and geological stability favour ND. Seed viability data show that campo rupestre species have a markedly low investment in regeneration from seeds, highlighting the need for specific in situ and ex situ conservation strategies to avoid loss of biodiversity.