Large-scale abandoned agricultural areas in Southeast Asia resulted in patches of forests of multiple successions and characteristics, challenging the study of their responses to environmental ...changes, especially under climatic water stress. Here, we investigated seasonal variation in leaf water status and drought tolerance of dominant tree species in three multi-aged tropical forests, ranging from 5 to > 200 years old, with contrasting soil moisture in Thailand. Seasonal variation in leaf water status differed among the forests with trees in young and intermediate sites demonstrating larger differences between seasons than the old-growth forest. Although vulnerability to embolism curves revealed that trees in old-growth forest were potentially more sensitive to declining leaf water status than others, they were predicted to lose < 5% of their hydraulic capacity as opposed to 13% for the trees in the younger sites. Our results suggest that the responses to water stress of tree species in different forest ages greatly vary with a tendency of trees in younger sites to be more resilience than those in older sites. Such information would benefit the selection of tree species that could adapt well to specific environments, thus improving the strategies for managing forests of different ages under a warmer future.
Soil respiration (SR) in forests contributes significant carbon dioxide emissions from terrestrial ecosystems and is highly sensitive to environmental changes, including soil temperature, soil ...moisture, microbial community, surface litter, and vegetation type. Indeed, a small change in SR may have large impacts on the global carbon balance, further influencing feedbacks to climate change. Thus, detailed characterization of SR responses to changes in environmental conditions is needed to accurately estimate carbon dioxide emissions from forest ecosystems. However, data for such analyses are still limited, especially in tropical forests of Southeast Asia where various stages of forest succession exist due to previous land‐use changes. In this study, we measured SR and some environmental factors including soil temperature (ST), soil moisture (SM), and organic matter content (OM) in three successional tropical forests in both wet and dry periods. We also analyzed the relationships between SR and these environmental variables. Results showed that SR was higher in the wet period and in older forests. Although no response of SR to ST was found in younger forest stages, SR of the old‐growth forest significantly responded to ST, plausibly due to the nonuniform forest structure, including gaps, that resulted in a wide range of ST. Across forest stages, SM was the limiting factor for SR in the wet period, whereas SR significantly varied with OM in the dry period. Overall, our results indicated that the responses of SR to environmental factors varied temporally and across forest succession. Nevertheless, these findings are still preliminary and call for detailed investigations on SR and its variations with environmental factors in Southeast Asian tropical forests where patches of successional stages dominate.
We measured and analyzed soil respiration (SR) with environmental factors in three successional forests in Thailand. Results showed that SR was generally higher in the wet season and in older forests. Across all forest stages, soil moisture was the main factor contributing to variation in SR in the wet season while organic matter content played significant role in the dry season.
Abstract
Sapwood area is an important parameter for estimating canopy transpiration in the forest water cycle. However, sapwood area highly varies across species and forest ecosystems and is ...difficult to measure directly. Therefore, species- and site-specific allometric equations are needed to estimate the sapwood area of all trees in a forest. Here, we conducted a comprehensive campaign to measure sapwood thickness and to estimate the sapwood area of 14 common tree species in a successional forest in Thailand. These data represent the first comprehensive measurements of sapwood area in south-east Asian successional forests growing under diverse environmental conditions in terms of soil moisture and canopy density. The results show that a power function can significantly explain the relationship between sapwood area and stem size, represented by diameter at breast height (DBH), in all species in both primary and secondary forests. Interestingly, a single equation could describe the sapwood area~DBH relationship in all species and forest stages, except for Dipterocarpus gracilis, an emergent, dominant species in the primary forest. The latter showed slower growth in sapwood area once the trees reached a DBH of ~30 cm. Overall, our results can benefit future studies that estimate canopy transpiration of tropical forests with similar conditions as in our study sites.
•Liana abundance and diversity unexpectedly increased along a succession gradient.•Forest stages with homogeneous closed canopy could not inhibit colonization.•Size structure analysis indicated liana ...colonization along the succession gradient.•These results contradicted to all other studies of liana succession.•Community composition patterns are relatively more predictable in older ages.
One-half of the pantropical forests are regrowth that develop in certain stages along the succession gradient. As lianas can colonize rapidly in disturbed areas, they play a key role in forest succession and carbon sequestration. However, current knowledge remains limited and is from only a few sites in neotropical forests. Here we investigated liana succession in a chronosequence located in a Southeast Asian Forest. We determined liana abundance (stem density, basal area, prevalence) and diversity along the succession gradient with ages in the range 3–100 years. We also analyzed community composition, size structure, and the correlation with host tree size. We found that liana abundance and diversity increased non-linearly along the succession gradient, suggesting that the stem exclusion stage (35–41 years)—homogeneous closed canopy with low light penetration—did not inhibit liana colonization. Assuming the reverse J-shaped distribution, we fitted the size structure of each plot with the exponential distribution. The results demonstrated no differences among the fitted parameters of plots in the stem exclusion and the old-growth stage, suggesting the same capability of recruitment and colonization in both stages. Furthermore, we found a weak correlation between liana and host tree size (R2 ≤ 0.16, which varied among plots, implying that many lianas recruited after the establishment of large host trees in the past. The results regarding community composition perhaps suggested a stochastic process of liana colonization during the early stage (3–20 years) because of high spatial heterogeneity (a mosaic of open area alternating with closed canopy). In the stem exclusion and old-growth stages, we observed a predictable trajectory, with the composition of plots in the same stage being clustered. This implied that forest structure or unpredictable treefall gaps of old-growth forests have a limited impact on community dissimilarity. Collectively, these results suggested that (1) some liana species may be generalists or even shade-tolerant species, or (2) there was no seed dispersal limitation in the landscape. The contrary direction of the succession patterns reported here suggests a need for more studies across tropical forests including investigating life history trade-offs such as light tolerance.
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