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Summary: Nutrient limitation may constrain the ability of recovering and mature tropical forests to serve as a carbon sink. However, it is unclear to what extent trees can utilize nutrient acquisition strategies – especially root phosphatase enzymes and mycorrhizal symbioses – to overcome low nutrient availability across secondary succession.Using a large‐scale, full factorial nitrogen and phosphorus fertilization experiment of 76 plots along a secondary successional gradient in lowland wet tropical forests of Panama, we tested the extent to which root phosphatase enzyme activity and mycorrhizal colonization are flexible, and if investment shifts over succession, reflective of changing nutrient limitation. We also conducted a meta‐analysis to test how tropical trees adjust these strategies in response to nutrient additions and across succession.We find that tropical trees are dynamic, adjusting investment in strategies – particularly root phosphatase – in response to changing nutrient conditions through succession. These changes reflect a shift from strong nitrogen to weak phosphorus limitation over succession. Our meta‐analysis findings were consistent with our field study; we found more predictable responses of root phosphatase than mycorrhizal colonization to nutrient availability.Our findings suggest that nutrient acquisition strategies respond to nutrient availability and demand in tropical forests, likely critical for alleviating nutrient limitation. [ABSTRACT FROM AUTHOR]

Lianas are a prominent growth form in tropical forests, and there is compelling evidence that they are increasing in abundance throughout the Neotropics. While recent evidence shows that soil resources limit tree growth even in deep shade, the degree to which soil resources limit lianas in forest understories, where they coexist with trees for decades, remains unknown. Regardless, the physiological underpinnings of soil resource limitation in deeply shaded tropical habitats remain largely unexplored for either trees or lianas. Theory predicts that lianas should be more limited by soil resources than trees because they occupy the quick-return end of the "leaf economic spectrum," characterized by high rates of photosynthesis, high specific leaf area, short leaf life span, affinity to high-nutrient sites, and greater foliar nutrient concentrations. To address these issues, we asked whether soil resources (nitrogen, phosphorus, and potassium), alone or in combination, applied experimentally for more than a decade would cause significant changes in the morphology or physiology of tree and liana seedlings in a lowland tropical forest. We found evidence for the first time that phosphorus limits the photosynthetic performance of both trees and lianas in deeply shaded understory habitats. More importantly, lianas always showed significantly greater photosynthetic capacity, quenching, and saturating light levels compared to trees across all treatments. We found little evidence for nutrient x growth form interactions, indicating that lianas were not disproportionately favored in nutrient-rich habitats. Tree and liana seedlings differed markedly for six key morphological traits, demonstrating that architectural differences occurred very early in ontogeny prior to lianas finding a trellis (all seedlings were self-supporting). Overall, our results do not support nutrient loading as a mechanism of increasing liana abundance in the Neotropics. Rather, our finding that lianas always outperform trees, in terms of photosynthetic processes and under contrasting rates of resource supply of macronutrients, will allow lianas to increase in abundance if disturbance and tree turnover rates are increasing in Neotropical forests as has been suggested.

1. Nutrients are a critical resource for plant growth, but the elements limiting growth in tropical forests have rarely been determined. 2. We investigated the influence of nitrogen (N), phosphorus (P), potassium (K) and micronutrients on seedling biomass and nutrient allocation in a factorial nutrient fertilization experiment in lowland tropical forest at the Barro Colorado Nature Monument, Panama. We also measured 8 years of herbivory and growth for 1800 seedlings. We sought to determine the identity of limiting elements and possible nutrient interactions. 3. The five study species were Alseis blackiana, Desmopsis panamensis, Heisteria concinna, Sorocea affinis and Tetragastris panamensis. Plants grew in deeply shaded understorey with a mean canopy openness of 4.9% (±0.7%; 1 SE). 4. Tissue N concentration increased by 11% with N addition. Tissue P concentration increased by 16% with P addition. Tissue K increased by 4% with K addition. K addition reduced root‐to‐shoot biomass ratio. There was no significant effect of fertilization on specific leaf area or leaf area ratio. 5. The proportion of leaves damaged and the mean level of damage by herbivory increased with P and K addition and showed a significant P × K interaction. 6.7ensp;Across all species and years, relative growth rate of height increased with K addition and with N and P in combination. Relative growth rate of leaf count trended 8.5% higher with K addition (P = 0.076). 7. We also added micronutrients in a parallel experiment. There was no effect of micronutrient addition on any seedling parameter. 8. Synthesis. K addition affected seedlings by enhancing tissue nutrient concentration, increasing herbivory, reducing root‐to‐shoot biomass ratio and increasing height growth. Additional effects of N or P on tissue chemistry, herbivory and growth offer support for the multiple limiting resources hypothesis. Our results suggest that seedling growth is limited by nutrients, especially K, even under highly shaded conditions in this lowland tropical forest.

We maintained a factorial nitrogen (N), phosphorus (P), and potassium (K) addition experiment for 11 years in a humid lowland forest growing on a relatively fertile soil in Panama to evaluate potential nutrient limitation of tree growth rates, fine-litter production, and fine-root biomass. We replicated the eight factorial treatments four times using 32 plots of 40 x 40 m each. The addition of K was associated with significant decreases in stand-level fine-root biomass and, in a companion study of seedlings, decreases in allocation to roots and increases in height growth rates. The addition of K and N together was associated with significant increases in growth rates of saplings and poles (1-10 cm in diameter at breast height) and a further marginally significant decrease in stand-level fine-root biomass. The addition of P was associated with a marginally significant (P = 0.058) increase in fine-litter production that was consistent across all litter fractions. Our experiment provides evidence that N, P, and K all limit forest plants growing on a relatively fertile soil in the lowland tropics, with the strongest evidence for limitation by K among seedlings, saplings, and poles.

Nutrient addition experiments indicate that nitrogen and phosphorus limit plant processes in many tropical forests. However, the long‐term consequences for forest structure and species composition remain unexplored. We are positioned to evaluate potential long‐term consequences of nutrient addition in central Panama where we have maintained a factorial nitrogen–phosphorus–potassium fertilization experiment for 21 yr and an independent study quantified the species‐specific nutrient requirements of 550 local tree species. Here, we ask whether nutrients limit reproduction at the species and community levels. We also ask whether species‐specific reproductive responses to nutrient addition are stronger among species associated with naturally fertile soils, which could contribute to a shift in species composition. We quantified species‐level reproductive responses for 38 focal species in the 21st year of the experiment and community‐level reproductive litter production for the first 20 yr. Species‐level reproductive responses to nitrogen and potassium addition were weak, inconsistent across species, and insignificant across the 38 focal species. In contrast, species‐level responses to phosphorus addition were consistently and significantly positive across the 38 focal species but were unrelated to species‐specific phosphorus requirements documented independently for the same species. Community‐level reproductive litter production was unaffected by nutrient addition, possibly because spatial and temporal variation is large. We conclude that phosphorus limits reproduction by trees in our experiment but find no evidence that reproductive responses to phosphorus addition favor species associated with naturally phosphorus‐rich soils. [ABSTRACT FROM AUTHOR]

Myxomycetes (plasmodial slime molds) are abundant protist predators that feed on bacteria and other microorganisms, thereby playing important roles in terrestrial nutrient cycling. Despite their significance, little is known about myxomycete communities and the extent to which they are affected by nutrient availability. We studied the influence of long‐term addition of N, P, and K on the myxomycete community in a lowland forest in the Republic of Panama. In a previous study, microbial biomass increased with P but not N or K addition at this site. We hypothesized that myxomycetes would increase in abundance in response to P but that they would not respond to the sole addition of N or K. Moist chamber cultures of leaf litter and small woody debris were used to quantify myxomycete abundance. We generated the largest myxomycete dataset (3,381 records) for any single locality in the tropics comprised by 91 morphospecies. In line with our hypothesis, myxomycete abundance increased in response to P addition but did not respond to N or K. Community composition was unaffected by nutrient treatments. This work represents one of very few large‐scale and long‐term field studies to include a heterotrophic protist highlighting the feasibility and value in doing so. [ABSTRACT FROM AUTHOR]

Human activities are rapidly changing biogeochemistry across the globe, yet little is known about biogeochemical impacts on higher-level consumers. In a Panamanian rainforest, we measured the effects of chronic nitrogen, phosphorus, and potassium fertilization on ants: hyper-abundant terrestrial arthropods and ecosystem engineers. We tested two compatible hypotheses: the nutrient limitation hypothesis-where adding a limiting nutrient increases ant activity and abundance; and the community homogenization hypothesis-where adding a limiting nutrient decreases ant diversity. Lowland tropical rainforests are expected to be phosphorus-limited, so we predicted higher ant activity but lower diversity on phosphorus plots. In each fertilization plot, we baited trees and lianas to attract both canopy and ground nesting ants. After controlling for temperature, which accounted for roughly 20% of the variation in ant foraging activity, ant activity remained higher on phosphorus addition plots than on any other fertilization treatment. Genus level diversity was 16% lower on plots receiving phosphorus than the control, consistent with the paradox of enrichment frequently observed in plant communities. This pattern, however, did not hold for species level diversity. The community-level response was largely driven by the most abundant genus, Azteca, which increased foraging activity and abundance across phosphorus plots. The high activity and low diversity of ants on experimental phosphorus plots point to the potentially strong influence of biogeochemistry on these ubiquitous insects with potential ramifications for the forest food web. This is, to our knowledge, the first study relating biogeochemistry of macronutrients to foraging activity, diversity, and abundance of consumers, implicating strong bottom-up structuring of the ant community in one of the world's most diverse ecosystems. [ABSTRACT FROM AUTHOR]

I present a meta‐analysis of plant responses to 48 nutrient addition experiments conducted with native species in naturally growing tropical forests, exclusive of mangrove forests. The added nutrients include nitrogen (N) in 36 experiments, phosphorus (P) in 33 experiments, calcium and potassium in one experiment each, and various mixtures of essential nutrients in the remaining experiments. I evaluate the hypotheses that nutrients limit tropical forest plants, nutrient limitation is stronger in successional than in old‐growth forests, P but not N is limiting in lowland forests, and N is limiting in montane forests. Responses to the most complete nutrient mix used in each experiment were strong for plant functions that contribute to aboveground production (Hedges' g averages 0.87) and nonsignificant for fine root biomass. Responses to N addition and to P addition were strong for tissue concentrations of the added element (Hedges' g averages 0.75 and 1.4, respectively), moderate for fine litter production (0.64 and 0.65, respectively), moderate to weak for plant growth (0.46 and 0.37, respectively) and nonsignificant for fine root biomass. Growth responses were stronger in successional than in old‐growth forests. All responses were unrelated to elevation. The 48 experiments included 30 factorial nitrogen‐phosphorus experiments that enable additional direct tests of the widely cited hypotheses that P limitation is stronger than N limitation in lowland forests and vice versa in montane forests. Both hypotheses were rejected. The N × P interaction effect was nonsignificant across the factorial experiments. In conclusion, nutrients clearly limit tropical forest plants. Limitation by N is widespread in both lowland and montane forests, and the same is true for P. Single experiments identify limitation by calcium and potassium, and correlative studies suggest limitation by calcium, potassium, and magnesium. The available evidence is consistent with the possibility that most macronutrients limit tropical forest plants; however, experiments focus almost exclusively on N and P. The way forward will include taking fuller advantage of existing nutrient addition experiments, siting new experiments strategically, and developing cost‐effective methods to assay responses to all of the essential nutrients soils supply to plants. [ABSTRACT FROM AUTHOR]