Worldwide decomposition rates depend both on climate and the legacy of plant functional traits as litter quality. To quantify the degree to which functional differentiation among species affects their litter decomposition rates, we brought together leaf trait and litter mass loss data for 818 species from 66 decomposition experiments on six continents. We show that: (i) the magnitude of species-driven differences is much larger than previously thought and greater than climate-driven variation; (ii) the decomposability of a species' litter is consistently correlated with that species' ecological strategy within different ecosystems globally, representing a new connection between whole plant carbon strategy and biogeochemical cycling. This connection between plant strategies and decomposability is crucial for both understanding vegetation-soil feedbacks, and for improving forecasts of the global carbon cycle.

Environmental conditions, dispersal lags, and interactions among species are major factors structuring communities through time and across space. Ecologists have emphasized the importance of biotic interactions in determining local patterns of species association. In contrast, abiotic limits, dispersal limitation, and historical factors have commonly been invoked to explain community structure patterns at larger spatiotemporal scales, such as the appearance of late Pleistocene no‐analog communities or latitudinal gradients of species richness in both modern and fossil assemblages. Quantifying the relative influence of these processes on species co‐occurrence patterns is not straightforward. We provide a framework for assessing causes of species associations by combining a null‐model analysis of co‐occurrence with additional analyses of climatic differences and spatial pattern for pairs of pollen taxa that are significantly associated across geographic space. We tested this framework with data on associations among 106 fossil pollen taxa and paleoclimate simulations from eastern North America across the late Quaternary. The number and proportion of significantly associated taxon pairs increased over time, but only 449 of 56 194 taxon pairs were significantly different from random. Within this significant subset of pollen taxa, biotic interactions were rarely the exclusive cause of associations. Instead, climatic or spatial differences among sites were most frequently associated with significant patterns of taxon association. Most taxon pairs that exhibited co‐occurrence patterns indicative of biotic interactions at one time did not exhibit significant associations at other times. Evidence for environmental filtering and dispersal limitation was weakest for aggregated pairs between 16 and 11 kyr BP, suggesting enhanced importance of positive species interactions during this interval. The framework can thus be used to identify species associations that may reflect biotic interactions because these associations are not tied to environmental or spatial differences. Furthermore, temporally repeated analyses of spatial associations can reveal whether such associations persist through time.

Aim Biotic homogenization – the tendency for communities to converge in species composition – has occurred in many ecosystems, creating management challenges. The extent to which this convergence in species composition is related to convergence in trait composition (‘functional homogenization’), however, remains unresolved. Location North America, Wisconsin. Methods Using extensive plant community survey data from the 1950s and 2000s, and values for 11 traits measured on 169 species, we examined changes in functional beta diversity across 151 upland forest stands distributed across southern and northern Wisconsin. To estimate functional beta diversity, we used two recently developed pairwise functional dissimilarity metrics, plus an additive partitioning of functional diversity approach. Results Using pairwise functional dissimilarity metrics, we found no significant changes in functional beta diversity through time in either southern or northern upland forests. Under additive partitioning, species alpha diversity was lower than species beta diversity; whereas functional alpha diversity was much higher than functional beta diversity in both time periods and across all forest types. This suggests a high turnover of species but a low turnover of traits among communities. Main conclusions Although upland forests in Wisconsin have experienced taxonomic homogenization, they have not undergone functional homogenization, which may reflect a high functional redundancy among Wisconsin forest plants. As species decline further or disappear in response to habitat fragmentation and other global changes, functional redundancy may decline in a way that could diminish the functional diversity of Wisconsin's forests at both local and regional scales.

Question: What are the physical and chemical effects of plant litter on annual grassland community composition, aboveground net primary production (ANPP), and density? Location: California annual grassland. Methods: We manipulated litter and light levels independently and in concert. Litter removal and litter addition treatments tested both the physical and chemical impacts of litter's presence. We additionally simulated the effect of litter physical shading by using shade cloth, and added powdered litter to test for the chemical impacts of decomposing litter. Results: Increased whole litter and shading decreased grass germination and establishment, but not that of forbs or legumes. Species shifts occurred within all groups across treatments, including a transition from small-seeded to large-seeded grass and legume species with increased shading. ANPP was highest in control plots (473 ± 59 g/m 2 ), and species richness was highest in litter removal plots. While the physical effects of litter via shading were significant, the chemical effects of adding powdered litter were negligible. Conclusions: This work suggests that over one growing season, the physical impacts of litter are more important than chemical impacts in shaping community structure and ANPP in annual grasslands. Changes in light availability with altered litter inputs drive shifts in species and functional group composition. Litter feedbacks to ANPP and species composition of local patches may help maintain diversity and stabilize ANPP in this grassland.

Temperate North American forest communities have changed considerably in response to logging, fragmentation, herbivory, and other global change factors. Significant changes in the structure and composition of seemingly undisturbed Wisconsin forest communities have occurred over the past 50 years, including widespread declines in alpha and beta species diversity. To investigate how shifts in species composition have affected distributions of plant functional traits, we first compiled extensive data on understory plant species traits. We then computed community-weighted trait means and functional diversity metrics for communities in both the 1950s and 2000s. We examined how trait values and diversity varied across environmental gradients and among Wisconsin's four main ecoregions. Trait means and diversity values reflect conspicuous gradients in species composition, soils, and climatic conditions. Over the past 50 years, values of most traits have changed as communities shifted toward species with higher leaf nutrient levels and specific leaf area, particularly in the southern ecoregions. Trait richness and diversity have declined, particularly in historically species- and trait-rich unglaciated southwestern Wisconsin. Reductions in within-site trait diversity may be diminishing the ability of these forest communities to resist or resiliently respond to shifts in environmental conditions. Despite changes in trait and community composition, trait-environment relationships measured directly via fourth-corner analysis remain strong for most plant traits. Nevertheless, accelerating ecological change (including climate change) could outstrip the ability of plant species and traits to match their environment, particularly in more fragmented landscapes.

Understanding how ecological communities are organized and how they change through time is critical to predicting the effects of climate change. Recent work documenting the co-occurrence structure of modern communities found that most significant species pairs co-occur less frequently than would be expected by chance. However, little is known about how co-occurrence structure changes through time. Here we evaluate changes in plant and animal community organization over geological time by quantifying the co-occurrence structure of 359,896 unique taxon pairs in 80 assemblages spanning the past 300 million years. Co-occurrences of most taxon pairs were statistically random, but a significant fraction were spatially aggregated or segregated. Aggregated pairs dominated from the Carboniferous period (307 million years ago) to the early Holocene epoch (11,700 years before present), when there was a pronounced shift to more segregated pairs, a trend that continues in modern assemblages. The shift began during the Holocene and coincided with increasing human population size and the spread of agriculture in North America. Before the shift, an average of 64% of significant pairs were aggregated; after the shift, the average dropped to 37%. The organization of modern and late Holocene plant and animal assemblages differs fundamentally from that of assemblages over the past 300 million years that predate the large-scale impacts of humans. Our results suggest that the rules governing the assembly of communities have recently been changed by human activity.

Aim  Plant communities across the temperate zone are changing in response to successional processes and human‐induced disturbances. Here, we assess how upland forest under‐ and overstorey community composition has changed along an edaphic gradient. Location  Northern Wisconsin, USA. Methods  Forest sites initially sampled in the 1950s were resampled for overstorey composition and diversity, basal area, and understorey composition and diversity. We used clustering methods to identify groups of stands based on overstorey composition, and we used similarity indices, ordination and diversity indices to evaluate changes in species abundance and overall community structure. Results  Sites clustered into four overstorey groups along the edaphic gradient: ‘hemlock’ sites dominated by hemlock in 1950, ‘mesic’ sites dominated by northern hardwoods, ‘dry’ sites with a significant pine inclusion in the canopy and diverse ‘dry‐mesic’ sites in the middle. Collectively, forests gained maple, ash and cherry while losing pines, birches and red oaks. The hemlock forest sites gained hardwoods, while the dry‐mesic sites shifted towards a more mesic hardwood composition. Only the driest sites have remained relatively stable in species composition. Main conclusions  These trends reflect both ‘mesification’ and homogenization among northern forests. Highly diverse mid‐gradient and mesic hemlock‐dominated stands are transitioning to maple dominance. Fire suppression may be favouring invasions of more mesic plants into historically drier sites, while high deer abundance likely limits hemlock regeneration. If current trends continue, maples will dominate the majority of northern forests, with significant losses of local native species richness and substantial shifts in understorey composition.

Questions: Do ecological sorting processes and functional diversity of forest ground-layer plant communities vary among mature (65-85-yr-old) even-aged, managed uneven-aged and old-growth forest stands? How does functional diversity relate to environmental variables within stands? Location: Northern temperate deciduous forests of Wisconsin and the Upper Peninsula of Michigan, USA. Methods: Ground-layer species cover and light availability were measured at each of four old-growth, even-aged second-growth, and managed uneven-aged stands (n = 12 stands total). We used mixed-effect models and fourth-corner analysis to assess relationships among forest structure, species traits and the three components of functional diversity (functional richness, evenness, divergence) based on 32 leaf, reproductive and whole plant traits from 111 species. Results: We identified differences in leaf phenology and morphology, life form and dispersal among stand types at the community level. Ground-layer plant communities of even-aged and uneven-aged stands were at opposite ends of a spectrum of strategies aimed at tolerating stressful vs competitive environments, respectively. In even-aged stands, communities were characterized by species adapted to relatively dark and closed conditions (heavy-seeded tree saplings, spring ephemerals). In contrast, managed uneven-aged stands were characterized by species with potential for quick returns on investment of nutrients and dry mass in leaves (i.e. early summer species with high specific leaf area, low leaf dry matter content and high phosphorus concentration). Old-growth stands had fewer trait associations than managed stands, and were characterized by ferns and species with either ballistic or wind-assisted seed dispersal. Functional diversity metrics were related in complex ways to light, management and soil texture. Managed stands had higher functional richness and divergence than old-growth stands, which, instead, showed higher functional evenness. Conclusions: Even-aged and managed stands support ground-layer species with a distinct set of traits relative to those found in old-growth forests. Although there is broad interest in uneven-aged management as a means to restore the structures and functions of old-growth forests, uneven-aged management does not, at least initially, produce ground-layer plant communities more similar to old-growth forests than even-aged management. We elucidated a set of life-history traits providing a synthetic view of vegetation response to forest management. Functional diversity of ground-layer plant communities was related to differences in environmental conditions related to forest structure, suggesting that habitat filtering contributes to compositional differences at the community level. We discussed these differences with reference to plants' general strategies and carbon econom