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Interspecific differences in tree performance due to variation in resource availability are expected to influence the structure and dynamics of tropical forest communities. Patterns of mortality and growth over 32 mo in 11 species of Macaranga were analyzed to investigate factors influencing tree spatial distributions and the dynamics of early successional communities. Tree performance was assessed in relation to variation in light levels, soil texture, and tree ontogeny. Rates of mortality and growth varied by over an order of magnitude among species. Species common in high-light microsites had higher mortality and growth rates. Higher low-light mortality for these species reflected lower shade tolerances, supporting the view that shade tolerance involves a trade-off between high-light growth and low-light mortality. Logistic and multiple regressions were used to test for independent effects of tree size and microenvironment on performance in the 11 species. Mortality and growth were significantly related to tree size in nine and eight species, respectively. Higher mortality and lower growth rates for juvenile trees were common. Despite positive correlations between light availability and tree size, mortality rates increased in three species, and growth rates decreased in four species at larger tree sizes. This pattern was particularly strong in smaller statured shade-intolerant species and may reflect changes in biomass allocation following reproductive onset. Declines in growth at larger tree sizes for only some species resulted in changes in species' performance rankings through succession. Low-light mortality rates were strongly correlated with species' distributions in the forest with respect to light levels, whereas biases in distributions with respect to soil texture were not supported by differential mortality. For all trees pooled and in several species, growth showed a threshold response to light levels, being light-limited in low light but not in high light. Across all light levels, soil texture significantly influenced growth in six species. Five species and all trees pooled had significantly lower growth on the more nutrient-poor and potentially drought-prone sandy soils. The dynamics of Macaranga-dominated early successional communities are strongly influenced by soil resource and light availability, coupled with species-specific ontogenetic trajectories of performance.

To examine interspecific variation in the intensity of ant defense among three sympatric species of obligate myrmecophytes of Macaranga (Euphorbiaceae), we measured the ratio of ant biomass to plant biomass, ant aggressiveness to artificial damage on host plants, and increase in herbivore damage on host plants when symbiont ants were removed. Increase in herbivore damage from two- and four-week ant exclusion varied significantly among the three species. The decreasing order of vulnerability to herbivory was M. winkleri, M. trachyphylla, and M. beccariana. The ant/plant biomass ratio (= rate of the dry weight of whole ant colonies to the dry weight of whole aboveground plant parts) and ant agressiveness also varied significantly among the three species; the orders of both the ant/plant biomass ratio and ant aggressiveness were the same as in the herbivory increase. These results indicated that the intensity of ant defense differs predictably among sympatric species of obligate myrmecophytes on Macaranga. In addition to the interspecific difference in the total intensity of ant defense, when symbiont ants were excluded, both patterns of within-plant variation in the amount of herbivore damage and compositions of herbivore species that caused the damage differed among species. This suggests that the three Macaranga species have different systems of ant defense with reference to what parts of plant tissue are protected and what herbivorous species are avoided by ant defense. Thus, it is important to consider the interspecific variation in ant defense among Macaranga species to understand the herbivore community on Macaranga plants and the mechanisms that promote the coexistence of multiple Macaranga myrmecophytes.

To examine interspecific variation in the intensity of ant defense among three sympatric species of obligate myrme‐cophytes of Macaranga (Euphorbiaceae), we measured the ratio of ant biomass to plant biomass, ant aggressiveness to artificial damage on host plants, and increase in herbivore damage on host plants when symbiont ants were removed. Increase in herbivore damage from two‐ and four‐week ant exclusion varied significantly among the three species. The decreasing order of vulnerability to herbivory was M. winkleri, M. trachyphylla, and M. beccariana. The antip/ant biomass ratio (= rate of the dry weight of whole ant colonies to the dry weight of whole aboveground plant parts) and ant agressiveness also varied significantly among the three species; the orders of both the ant/plant biomass ratio and ant aggressiveness were the same as in the herbivory increase. These results indicated that the intensity of ant defense differs predictably among sympatric species of obligate myrmecophytes on Macaranga. In addition to the interspecific difference in the total intensity of ant defense, when symbiont ants were excluded, both patterns of within‐plant variation in the amount of herbivore damage and compositions of herbivore species that caused the damage differed among species. This suggests that the three Macaranga species have different systems of ant defense with reference to what parts of plant tissue are protected and what herbivorous species are avoided by ant defense. Thus, it is important to consider the interspecific variation in ant defense among Macaranga species to understand the herbivore community on Macaranga plants and the mechanisms that promote the coexistence of multiple Macaranga myrmecophytes.

To examine interspecific variation in the intensity of ant defense among three sympatric species of obligate myrmecophytes of Macaranga (Euphorbiaceae), we measured the ratio of ant biomass to plant biomass, ant aggressiveness to artificial damage on host plants, and increase in herbivore damage on host plants when symbiont ants were removed. Increase in herbivore damage from two- and four-week ant exclusion varied significantly among the three species. The decreasing order of vulnerability to herbivory was M. winkleri, M. trachyphylla, and M. beccariana. The ant/plant biomass ratio (= rate of the dry weight of whole ant colonies to the dry weight of whole aboveground plant parts) and ant agressiveness also varied significantly among the three species; the orders of both the ant/plant biomass ratio and ant aggressiveness were the same as in the herbivory increase. These results indicated that the intensity of ant defense differs predictably among sympatric species of obligate myrmecophytes on Macaranga. In addition to the interspecific difference in the total intensity of ant defense, when symbiont ants were excluded, both patterns of within-plant variation in the amount of herbivore damage and compositions of herbivore species that caused the damage differed among species. This suggests that the three Macaranga species have different systems of ant defense with reference to what parts of plant tissue are protected and what herbivorous species are avoided by ant defense. Thus, it is important to consider the interspecific variation in ant defense among Macaranga species to understand the herbivore community on Macaranga plants and the mechanisms that promote the coexistence of multiple Macaranga myrmecophytes.