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  1. Abstract Exotic tree species, though widely used in forestry and restoration projects, pose great threats to local ecosystems. They need to be replaced with native species from natural forests. We hypothesized that natural forests contain large, fast-growing, dominant native tree species that are suitable for specific topographic conditions in forestry. We tested this hypothesis using data from a 50-ha forest dynamics plot in subtropical China. We classified the plot into the ridge, slope, and valley habitats and found that 34/87 species had significant associations with at least one topographic habitat. There were 90 tree species with a maximum diameter ≥ 30 cm, and their abundances varied widely in all habitat types. In all habitat types, for most species, rate of biomass gain due to recruitment was < 1% of its original biomass, and rate of biomass gain due to tree growth was between 1 and 5% of its original biomass. For most species, biomass loss due to tree mortality was not significantly different than biomass gain due to recruitment, but the resulting net biomass increment rates did not significantly differ from zero. The time required to reach a diameter of 30 cm from 1 cm diameter forAltingia chinensisin the slope habitat, forQuercus chungiiandMorella rubrain the ridge habitat and forCastanopsis carlesiiin all habitats could be as short as 30 years in our simulations based on actual distributions of tree growth observed in the forest. Principal component analyses of maximum diameter, abundance and net biomass increment rates suggested several species were worthy of further tests for use in forestry.Our study provides an example for screening native tree species from natural forests for forestry. Because native tree species are better for local ecosystems, our study will also contribute to biodiversity conservation in plantations. 
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  2. Abstract Over 125 million years of ant-plant interactions have culminated in one of the most intriguing evolutionary outcomes in life history. The myrmecophyteDuroia hirsuta(Rubiaceae) is known for its mutualistic association with the antMyrmelachista schumanniand several other species, mainlyAzteca, in the north-western Amazon. While both ants provide indirect defences to plants, onlyM. schumanninests in plant domatia and has the unique behaviour of clearing the surroundings of its host tree from heterospecific plants, potentially increasing resource availability to its host. Using a 12-year survey, we asked how the continuous presence of either onlyM. schumannior onlyAztecaspp. benefits the growth and defence traits of host trees. We found that the continuous presence ofM. schumanniimproved relative growth rates and leaf shearing resistance ofDuroiabetter than trees withAzteca. However, leaf herbivory, dry matter content, trichome density, and secondary metabolite production were the same in all trees. Survival depended directly on ant association (> 94% of trees died when ants were absent). This study extends our understanding of the long-term effects of strict ant-plant mutualism on host plant traits in the field and reinforces the use ofD. hirsuta–M. schumannias a model system suitable for eco-co-evolutionary research on plant–animal interactions. 
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  3. Abstract The Andes are a major dispersal barrier for lowland rain forest plants and animals, yet hundreds of lowland tree species are distributed on both sides of the northern Andes, raising questions about how the Andes influenced their biogeographic histories and population genetic structure. To explore these questions, we generated standardized datasets of thousands of SNPs from paired populations of 49 tree species co‐distributed in rain forest tree communities located in Panama and Amazonian Ecuador and calculated genetic diversity (π) and absolute genetic divergence (dXY) within and between populations, respectively. We predicted (1) higher genetic diversity in the ancestral source region (east or west of the Andes) for each taxon and (2) correlation of genetic statistics with species attributes, including elevational range and life‐history strategy. We found that genetic diversity was higher in putative ancestral source regions, possibly reflecting founder events during colonization. We found little support for a relationship between genetic divergence and species attributes except that species with higher elevational range limits exhibited higherdXY, implying older divergence times. One possible explanation for this pattern is that dispersal through mountain passes declined in importance relative to dispersal via alternative lowland routes as the Andes experienced uplift. We found no difference in mean genetic diversity between populations in Central America and the Amazon. Overall, our results suggest that dispersal across the Andes has left enduring signatures in the genetic structure of widespread rain forest trees. We outline additional hypotheses to be tested with species‐specific case studies. 
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  4. Abstract Growing evidence suggests that liana competition with trees is threatening the global carbon sink by slowing the recovery of forests following disturbance. A recent theory based on local and regional evidence further proposes that the competitive success of lianas over trees is driven by interactions between forest disturbance and climate. We present the first global assessment of liana–tree relative performance in response to forest disturbance and climate drivers. Using an unprecedented dataset, we analysed 651 vegetation samples representing 26,538 lianas and 82,802 trees from 556 unique locations worldwide, derived from 83 publications. Results show that lianas perform better relative to trees (increasing liana‐to‐tree ratio) when forests are disturbed, under warmer temperatures and lower precipitation and towards the tropical lowlands. We also found that lianas can be a critical factor hindering forest recovery in disturbed forests experiencing liana‐favourable climates, as chronosequence data show that high competitive success of lianas over trees can persist for decades following disturbances, especially when the annual mean temperature exceeds 27.8°C, precipitation is less than 1614 mm and climatic water deficit is more than 829 mm. These findings reveal that degraded tropical forests with environmental conditions favouring lianas are disproportionately more vulnerable to liana dominance and thus can potentially stall succession, with important implications for the global carbon sink, and hence should be the highest priority to consider for restoration management. 
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  5. Life‐history strategies emerge from eco‐evolutionary constraints, where organisms allocate limited resources to growth, survival, and reproduction, resulting in trade‐offs such as the growth–survival trade‐off. There is still a limited understanding of whether and how disturbance regimes and successional stages might mediate such trade‐offs, with potential consequences for species population dynamics and community assembly. Here, we investigate how disturbances shape the growth–survival trade‐off by comparing early and late‐successional forest stands across the eastern United States. Using large‐scale sampling to capture the realised niche of 68 temperate species, we estimated species‐specific mortality probabilities under zero growth (a proxy for resource‐poor environments) applying a Bayesian multilevel modelling framework. We tested trade‐offs between these estimates and species' maximum growth capacity (a proxy for resource‐rich environments), within and across early and late‐successional stands. Overall, we found a weak growth–survival trade‐off among temperate tree species. No clear evidence of this trade‐off was found in early successional stands , while late‐successional stands showed a relatively stronger—though still weak—positive association between species' maximum growth and mortality under zero growth conditions. Disturbances therefore seem to mediate a filtering of tree life‐history strategies. Consequently, an increase in disturbance rates or changes in their regime could disrupt the growth–survival trade‐off in temperate forests. Life‐history strategies arise from eco‐evolutionary constraints and can lead to trade‐offs like tree growth and survival. While temperate tree species in late‐successional or low‐disturbance‐frequency forests do show a growth–survival trade‐off, this trade‐off is weak and was not found in early successional or high‐disturbance‐frequency stands, nor across all stages combined. Our findings highlight a role of disturbances in filtering life‐history strategies and their potential impact on forest dynamics and global carbon cycling but also a need to better understand the mediating processes of tree demographic trade‐offs. 
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  6. It is widely recognized that large‐scale topographic variation affects the distribution of tree diversity, yet the effects of topography at smaller scales are less appreciated but can be no less consequential. We evaluated how small‐scale topographic variation affects tree demography and diversity in a hyperdiverse Amazonian forest where species distributions respond strongly to elevation differences as small as 22 m. For topographically structured species distributions to arise, species should grow and survive (perform) better in the topographic habitat they are associated with, and they should outperform other species that are found, but not strongly aggregated, in that habitat. Here, we tested these demographic hypotheses using data on the growth and mortality of 79,911 trees (352 species) among three topographic habitats (valleys, slopes and ridges) in the 25‐ha Amacayacu Forest Dynamics Plot.Despite the small variation in elevation, there was significant community‐level variation in growth and mortality among topographic habitats: trees growing in valleys, where soil moisture is higher, had significantly higher growth and mortality rates than those growing on slopes and ridges. However, tree growth rates did not depend on, and mortality rates varied inconsistently with, species' habitat association. Our results partially support the resident‐advantage hypotheses for valley‐associated species, which grew best in their home habitat (valleys) than elsewhere and had lower mortality there compared to slope‐associated or generalist species (foreigners). For slope‐ and ridge‐associated species, our results did not support these hypotheses at the community level. Species‐specific analyses revealed that 73 out of the 352 species analysed at the community level supported either hypothesis. Our findings show that even small differences in elevation can lead to biologically meaningful variation in resource access that translates into significant differences in tree growth and survival. However, resource access could not fully explain the patterns of topographically driven demographic variation we observed. While certain species may still exhibit home and resident advantages in specific habitats, even when community‐level averages partially reflect this pattern, alternative hypotheses are likely driving the patterns observed at the community level. 
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  7. Tree growth and longevity trade-offs fundamentally shape the terrestrial carbon balance. Yet, we lack a unified understanding of how such trade-offs vary across the world’s forests. By mapping life history traits for a wide range of species across the Americas, we reveal considerable variation in life expectancies from 10 centimeters in diameter (ranging from 1.3 to 3195 years) and show that the pace of life for trees can be accurately classified into four demographic functional types. We found emergent patterns in the strength of trade-offs between growth and longevity across a temperature gradient. Furthermore, we show that the diversity of life history traits varies predictably across forest biomes, giving rise to a positive relationship between trait diversity and productivity. Our pan-latitudinal assessment provides new insights into the demographic mechanisms that govern the carbon turnover rate across forest biomes. 
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  8. The interspecific trade‐off between growth versus mortality rates of tree species is thought to be driven by functional biology and to contribute to species ecological niche differentiation. Yet, functional trait variation is often not strongly correlated with growth and mortality, and few studies have investigated the relationships of both traits and niches, specifically encompassing above and belowground resources, to the trade‐off itself. These relationships are particularly relevant for seedlings, which must often survive resource limitation to reach larger size classes.We investigated the functional basis of the interspecific growth–mortality trade‐off and its relationship with ecological niches for seedlings of 14 tree species in a tropical forest in southwest China.We found evidence for an interspecific growth–mortality trade‐off at the seedling stage using 15 functional traits and 15 ecological niche variables. None of the organ‐level traits correlated with growth, mortality, nor the trade‐off, whereas specific stem length (SSL), a biomass allocation trait, was the only trait to have a significant correlation (positive). Moreover, light‐defined niches were not correlated with growth, mortality or the trade‐off, but soil‐defined niches did. Species at the faster growth/higher mortality end of the trade‐off were associated with higher fertility defined by lower soil bulk density and slope, and higher soil organic matter concentration and soil total nitrogen.Our findings indicate the importance of stem elongation and soil fertility for growth, mortality and their trade‐off at the seedling stage in this Asian tropical forest. Our findings contrast with analogous studies in neotropical forests showing the importance of photosynthesis‐related leaf traits related to insolation. Therefore, the functional drivers of demographic rates and trade‐offs, as well as their consequences for ecological niches, can vary among forests, likely owing to differences in biogeography, canopy disturbance rates, topography and soil properties. Moreover, the effects of functional trait variation on demographic rates and trade‐offs may be better revealed when biomass allocation is accounted for in a whole‐plant context. Read the freePlain Language Summaryfor this article on the Journal blog. 
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