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  1. Abstract

    Numerous studies have shown reduced performance in plants that are surrounded by neighbours of the same species1,2, a phenomenon known as conspecific negative density dependence (CNDD)3. A long-held ecological hypothesis posits that CNDD is more pronounced in tropical than in temperate forests4,5, which increases community stabilization, species coexistence and the diversity of local tree species6,7. Previous analyses supporting such a latitudinal gradient in CNDD8,9have suffered from methodological limitations related to the use of static data10–12. Here we present a comprehensive assessment of latitudinal CNDD patterns using dynamic mortality data to estimate species-site-specific CNDD across 23 sites. Averaged across species, we found that stabilizing CNDD was present at all except one site, but that average stabilizing CNDD was not stronger toward the tropics. However, in tropical tree communities, rare and intermediate abundant species experienced stronger stabilizing CNDD than did common species. This pattern was absent in temperate forests, which suggests that CNDD influences species abundances more strongly in tropical forests than it does in temperate ones13. We also found that interspecific variation in CNDD, which might attenuate its stabilizing effect on species diversity14,15, was high but not significantly different across latitudes. Although the consequences of these patterns for latitudinal diversity gradients are difficult to evaluate, we speculate that a more effective regulation of population abundances could translate into greater stabilization of tropical tree communities and thus contribute to the high local diversity of tropical forests.

     
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    Free, publicly-accessible full text available March 21, 2025
  2. Abstract

    Increasing temperatures and human activity are likely to reduce fire return intervals in the seasonal tropics. Anticipating how more frequent fires may alter forest community structure and composition requires understanding how fire intensity and species‐specific responses to fires interact to drive fire‐induced mortality for large numbers of species. We developed an analytical framework to estimate unobserved fire intensities and species‐ and size‐specific susceptibility to fire using observed mortality data.

    We used census data from a 50‐ha forest dynamics plot in western Thailand to better understand species and community responses to a fire that burned60% of the plot in 2005. Trees species, size and status (live, dead) were censused just before the fire (2004) and again 5 years later (2009). We jointly estimated a map of relative fire intensity and species‐specific size‐dependent background and fire‐induced mortality. We then calculated the time required for individuals of each species to reach a fire‐safe size threshold (the age at which the fire‐induced mortality probability was <50%). To better understand community‐level responses to fire, we compared results among different species groups (canopy status, forest‐type association).

    Our model‐derived map of fire intensity closely matched the field survey taken in the days after the fire. On average, individuals growing at the 95th percentile growth rate for most species groups required5 years to reach their species’ fire‐safe size threshold, while individuals growing at the median growth rate required17 years (assuming growth <1 cm diameter at breast height was similar to growth >1 cm). However, understorey species associated with the seasonal evergreen forest took 1.8 times longer than average to reach their fire‐safe size threshold, with one species requiring up to 190 years.

    Synthesis.Our approach provided insights into spatial patterning of fire intensity in a seasonal tropical forest and species‐ and size‐specific susceptibility to fire‐induced mortality. Our results suggest increasing fire frequency will have the greatest impact on slow‐growing understorey species of the evergreen forest. In addition, our model accurately predicts the growing dominance of a fast‐growing understorey species,Croton roxburghii;Euphorbiaceae, common to evergreen and deciduous forests that can reach its fire‐safe size threshold in 1.3 years.

     
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  3. Abstract

    Organisms of all species must balance their allocation to growth, survival and recruitment. Among tree species, evolution has resulted in different life‐history strategies for partitioning resources to these key demographic processes. Life‐history strategies in tropical forests have often been shown to align along a trade‐off between fast growth and high survival, that is, the well‐known fast–slow continuum. In addition, an orthogonal trade‐off has been proposed between tall stature—resulting from fast growth and high survival—and recruitment success, that is, a stature−recruitment trade‐off. However, it is not clear whether these two independent dimensions of life‐history variation structure tropical forests worldwide.

    We used data from 13 large‐scale and long‐term tropical forest monitoring plots in three continents to explore the principal trade‐offs in annual growth, survival and recruitment as well as tree stature. These forests included relatively undisturbed forests as well as typhoon‐disturbed forests. Life‐history variation in 12 forests was structured by two orthogonal trade‐offs, the growth−survival trade‐off and the stature−recruitment trade‐off. Pairwise Procrustes analysis revealed a high similarity of demographic relationships among forests. The small deviations were related to differences between African and Asian plots.

    Synthesis. The fast–slow continuum and tree stature are two independent dimensions structuring many, but not all tropical tree communities. Our discovery of the consistency of demographic trade‐offs and life‐history strategies across different forest types from three continents substantially improves our ability to predict tropical forest dynamics worldwide.

     
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  4. Abstract

    Despite benefits for precision, ecologists rarely use informative priors. One reason that ecologists may prefer vague priors is the perception that informative priors reduce accuracy. To date, no ecological study has empirically evaluated data‐derived informative priors' effects on precision and accuracy. To determine the impacts of priors, we evaluated mortality models for tree species using data from a forest dynamics plot in Thailand. Half the models used vague priors, and the remaining half had informative priors. We found precision was greater when using informative priors, but effects on accuracy were more variable. In some cases, prior information improved accuracy, while in others, it was reduced. On average, models with informative priors were no more or less accurate than models without. Our analyses provide a detailed case study on the simultaneous effect of prior information on precision and accuracy and demonstrate that when priors are specified appropriately, they lead to greater precision without systematically reducing model accuracy.

     
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  6. Abstract

    Tree rings provide an invaluable long‐term record for understanding how climate and other drivers shape tree growth and forest productivity. However, conventional tree‐ring analysis methods were not designed to simultaneously test effects of climate, tree size, and other drivers on individual growth. This has limited the potential to test ecologically relevant hypotheses on tree growth sensitivity to environmental drivers and their interactions with tree size. Here, we develop and apply a new method to simultaneously model nonlinear effects of primary climate drivers, reconstructed tree diameter at breast height (DBH), and calendar year in generalized least squares models that account for the temporal autocorrelation inherent to each individual tree's growth. We analyze data from 3811 trees representing 40 species at 10 globally distributed sites, showing that precipitation, temperature, DBH, and calendar year have additively, and often interactively, influenced annual growth over the past 120 years. Growth responses were predominantly positive to precipitation (usually over ≥3‐month seasonal windows) and negative to temperature (usually maximum temperature, over ≤3‐month seasonal windows), with concave‐down responses in 63% of relationships. Climate sensitivity commonly varied with DBH (45% of cases tested), with larger trees usually more sensitive. Trends in ring width at small DBH were linked to the light environment under which trees established, but basal area or biomass increments consistently reached maxima at intermediate DBH. Accounting for climate and DBH, growth rate declined over time for 92% of species in secondary or disturbed stands, whereas growth trends were mixed in older forests. These trends were largely attributable to stand dynamics as cohorts and stands age, which remain challenging to disentangle from global change drivers. By providing a parsimonious approach for characterizing multiple interacting drivers of tree growth, our method reveals a more complete picture of the factors influencing growth than has previously been possible.

     
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  7. Abstract

    Among the local processes that determine species diversity in ecological communities, fluctuation‐dependent mechanisms that are mediated by temporal variability in the abundances of species populations have received significant attention. Higher temporal variability in the abundances of species populations can increase the strength of temporal niche partitioning but can also increase the risk of species extinctions, such that the net effect on species coexistence is not clear. We quantified this temporal population variability for tree species in 21 large forest plots and found much greater variability for higher latitude plots with fewer tree species. A fitted mechanistic model showed that among the forest plots, the net effect of temporal population variability on tree species coexistence was usually negative, but sometimes positive or negligible. Therefore, our results suggest that temporal variability in the abundances of species populations has no clear negative or positive contribution to the latitudinal gradient in tree species richness.

     
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