76 research outputs found
Thinner bark increases sensitivity of wetter Amazonian tropical forests to fire
Understory fires represent an accelerating threat to Amazonian tropical forests and can, during drought, affect larger areas than deforestation itself. These fires kill trees at rates varying from < 10 to c. 90% depending on fire intensity, forest disturbance history and tree functional traits. Here, we examine variation in bark thickness across the Amazon. Bark can protect trees from fires, but it is often assumed to be consistently thin across tropical forests. Here, we show that investment in bark varies, with thicker bark in dry forests and thinner in wetter forests. We also show that thinner bark translated into higher fireâdriven tree mortality in wetter forests, with between 0.67 and 5.86 gigatonnes CO2 lost in Amazon understory fires between 2001 and 2010. Traitâenabled global vegetation models that explicitly include variation in bark thickness are likely to improve the predictions of fire effects on carbon cycling in tropical forests
Individual-Based Modeling of Amazon Forests Suggests That Climate Controls Productivity While Traits Control Demography
Climate, species composition, and soils are thought to control carbon cycling and forest structure in Amazonian forests. Here, we add a demographics scheme (tree recruitment, growth, and mortality) to a recently developed non-demographic modelâthe Trait-based Forest Simulator (TFS)âto explore the roles of climate and plant traits in controlling forest productivity and structure. We compared two sites with differing climates (seasonal vs. aseasonal precipitation) and plant traits. Through an initial validation simulation, we assessed whether the model converges on observed forest properties (productivity, demographic and structural variables) using datasets of functional traits, structure, and climate to model the carbon cycle at the two sites. In a second set of simulations, we tested the relative importance of climate and plant traits for forest properties within the TFS framework using the climate from the two sites with hypothetical trait distributions representing two axes of functional variation (âfastâ vs. âslowâ leaf traits, and high vs. low wood density). The adapted model with demographics reproduced observed variation in gross (GPP) and net (NPP) primary production, and respiration. However, NPP and respiration at the level of plant organs (leaf, stem, and root) were poorly simulated. Mortality and recruitment rates were underestimated. The equilibrium forest structure differed from observations of stem numbers suggesting either that the forests are not currently at equilibrium or that mechanisms are missing from the model. Findings from the second set of simulations demonstrated that differences in productivity were driven by climate, rather than plant traits. Contrary to expectation, varying leaf traits had no influence on GPP. Drivers of simulated forest structure were complex, with a key role for wood density mediated by its link to tree mortality. Modeled mortality and recruitment rates were linked to plant traits alone, drought-related mortality was not accounted for. In future, model development should focus on improving allocation, mortality, organ respiration, simulation of understory trees and adding hydraulic traits. This type of model that incorporates diverse tree strategies, detailed forest structure and realistic physiology is necessary if we are to be able to simulate tropical forest responses to global change scenarios
The presence of peat and variation in tree species composition are under different hydrological controls in Amazonian wetland forests
This research was funded by the Gordon and Betty Moore Foundation, through grant #5349 âMonitoring protected areas in Peru to increase forest resilience to climate changeâ, and NERC standard grant âCarbon Storage in Amazonian Peatlands: Distribution and Dynamicsâ(NE/R000751/1).The peat-forming wetland forests of Amazonia are characterised by high below-carbon stocks and supply fruit, fibres and timber to local communities. Predicting the future of these ecosystem services requires understanding how hydrological conditions are related to tree species composition and the presence, or absence, of peat. Here, we use continuous measurements of water table depth over 2.5 years and manual measurements of pore-water pH and electrical conductivity to understand the ecohydrological controls of these variables across the large peatland complex in northern Peruvian Amazonia. Measurements were taken in permanent forest plots in four palm swamps, four seasonally flooded forests and four peatland pole forests. All trees â„10 cm diameter were also measured and identified in the plots to assess floristic composition. Peat occurs in eight of these twelve sites; three seasonally flooded forests and one palm swamp are not associated with peat. Variation in tree species composition among forest types was linked to high flood levels (maximum flooding height) and pH: seasonally flooded forests experience high flood levels (up to 3.66 m from the ground surface) and have high pH values (6?7), palm swamps have intermediate flood levels (up to 1.34 m) and peatland pole forests experience shallow flooding (up to 0.28 m) and have low pH (4). In contrast, the presence of peat was linked to variation in maximum water table depth (ie the depth to which the water table drops below the ground surface). Surface peat is found in all forest types where maximum water table depth does not fall >0.55 m below the ground surface at any time. Peat formation and variation in tree species composition therefore have different ecohydrological controls. Predicted increases in the frequency and strength of flooding events may alter patterns of tree species composition, whereas increases in drought severity and declines in minimum river levels may pose a greater risk to the belowground carbon stores of these peatland ecosystems.Publisher PDFPeer reviewe
Net primary productivity and litter decomposition rates in two distinct Amazonian peatlands
Measurements of net primary productivity (NPP) and litter decomposition from tropical peatlands are severely lacking, limiting our ability to parameterise and validate models of tropical peatland development and thereby make robust predictions of how these systems will respond to future environmental and climatic change. Here, we present total NPP (i.e., above- and below-ground) and decomposition data from two floristically and structurally distinct forested peatland sites within the Pastaza Marañón Foreland Basin, northern Peru, the largest tropical peatland area in Amazonia: (1) a palm (largely Mauritia flexuosa) dominated swamp forest and (2) a hardwood dominated swamp forest (known as âpole forestâ, due to the abundance of thin-stemmed trees). Total NPP in the palm forest and hardwood-dominated forest (9.83â±â1.43 and 7.34â±â0.84âMg C haâ»Âčâyearâ»Âč, respectively) was low compared with values reported for terra firme forest in the region (14.21â15.01âMg C haâ»Âčâyearâ»Âč) and for tropical peatlands elsewhere (11.06 and 13.20âMg C haâ»Âčâyearâ»Âč). Despite the similar total NPP of the two forest types, there were considerable differences in the distribution of NPP. Fine root NPP was seven times higher in the palm forest (4.56â±â1.05âMg C haâ»Âčâyearâ»Âč) than in the hardwood forest (0.61â±â0.22âMg C haâ»Âčâyearâ»Âč). Above-ground palm NPP, a frequently overlooked component, made large contributions to total NPP in the palm-dominated forest, accounting for 41% (14% in the hardwood-dominated forest). Conversely, Mauritia flexuosa litter decomposition rates were the same in both plots: highest for leaf material, followed by root and then stem material (21%, 77% and 86% of mass remaining after 1 year respectively for both plots). Our results suggest potential differences in these two peatland types' responses to climate and other environmental changes and will assist in future modelling studies of these systems
Fine root dynamics across pantropical rainforest ecosystems
Fine roots constitute a significant component of the net primary productivity (NPP) of forest ecosystems but are much less studied than aboveground NPP. Comparisons across sites and regions are also hampered by inconsistent methodologies, especially in tropical areas. Here, we present a novel dataset of fine root biomass, productivity, residence time, and allocation in tropical old-growth rainforest sites worldwide, measured using consistent methods, and examine how these variables are related to consistently determined soil and climatic characteristics. Our pantropical dataset spans intensive monitoring plots in lowland (wet, semi-deciduous, and deciduous) and montane tropical forests in South America, Africa, and Southeast Asia (n = 47). Large spatial variation in fine root dynamics was observed across montane and lowland forest types. In lowland forests, we found a strong positive linear relationship between fine root productivity and sand content, this relationship was even stronger when we considered the fractional allocation of total NPP to fine roots, demonstrating that understanding allocation adds explanatory power to understanding fine root productivity and total NPP. Fine root residence time was a function of multiple factors: soil sand content, soil pH, and maximum water deficit, with longest residence times in acidic, sandy, and water-stressed soils. In tropical montane forests, on the other hand, a different set of relationships prevailed, highlighting the very different nature of montane and lowland forest biomes. Root productivity was a strong positive linear function of mean annual temperature, root residence time was a strong positive function of soil nitrogen content in montane forests, and lastly decreasing soil P content increased allocation of productivity to fine roots. In contrast to the lowlands, environmental conditions were a better predictor for fine root productivity than for fractional allocation of total NPP to fine roots, suggesting that root productivity is a particularly strong driver of NPP allocation in tropical mountain regions.WHH was funded by Peruvian FONDECYT/CONCYTEC (grant contract number 213-2015-FONDECYT). The GEM network was supported by a European Research Council Advanced Investigator Grant to YM (GEM-TRAITS: 321131) under the European Union's Seventh Framework Programme (FP7/2007-2013). The field data collection was funded NERC Grants NE/D014174/1 and NE/J022616/1 for in Peru, BALI (NE/K016369/1) for work in Malaysia, the Royal Society-Leverhulme Africa Capacity Building Programme for work in Ghana and Gabon and ESPA-ECOLIMITS (NE/1014705/1) in Ghana and Ethiopia. Plot inventories in South America were supported by funding from the US National Science Foundation Long-Term Research in Environmental Biology program (LTREB; DEB 1754647) and the Gordon and Betty Moore Foundation Andes-Amazon Program. GEM data in Gabon were collected under authorization to YM and supported by the Gabon National Parks Agency. Y.M. is supported by the Jackson Foundation. We would like to acknowledge the GEM team across the tropical regions and countries of Bolivia, Brazil, Ghana, Gabon, Ethiopia, Malaysia, and Peru
Seasonal trends of Amazonian rainforest phenology, net primary productivity, and carbon allocation.:Seasonal trends of Amazonian forests.
The seasonality of solar irradiance and precipitation may regulate seasonal variations in tropical forests carbon cycling. Controversy remains over their importance as drivers of seasonal dynamics of net primary productivity in tropical forests. We use ground data from nine lowland Amazonian forest plots collected over 3 years to quantify the monthly primary productivity (NPP) of leaves, reproductive material, woody material, and fine roots over an annual cycle. We distinguish between forests that do not experience substantial seasonal moisture stress (âhumid sitesâ) and forests that experience a stronger dry season (âdry sitesâ). We find that forests from both precipitation regimes maximize leaf NPP over the drier season, with a peak in production in August at both humid (mean 0.39 ± 0.03 Mg C haâ1 monthâ1 in July, n = 4) and dry sites (mean 0.49 ± 0.03 Mg C haâ1 monthâ1 in September, n = 8). We identify two distinct seasonal carbon allocation patterns (the allocation of NPP to a specific organ such as wood leaves or fine roots divided by total NPP). The forests monitored in the present study show evidence of either (i) constant allocation to roots and a seasonal trade-off between leaf and woody material or (ii) constant allocation to wood and a seasonal trade-off between roots and leaves. Finally, we find strong evidence of synchronized flowering at the end of the dry season in both precipitation regimes. Flower production reaches a maximum of 0.047 ± 0.013 and 0.031 ± 0.004 Mg C haâ1 monthâ1 in November, in humid and dry sites, respectively. Fruitfall production was staggered throughout the year, probably reflecting the high variation in varying times to development and loss of fruit among species
Understanding different dominance patterns in western Amazonian forests
Dominance of neotropical tree communities by a few species is widely documented, but dominant trees show a variety of distributional patterns still poorly understood. Here, we used 503 forest inventory plots (93,719 individuals â„2.5 cm diameter, 2609 species) to explore the relationships between local abundance, regional frequency and spatial aggregation of dominant species in four main habitat types in western Amazonia. Although the abundance-occupancy relationship is positive for the full dataset, we found that among dominant Amazonian tree species, there is a strong negative relationship between local abundance and regional frequency and/or spatial aggregation across habitat types. Our findings suggest an ecological trade-off whereby dominant species can be locally abundant (local dominants) or regionally widespread (widespread dominants), but rarely both (oligarchs). Given the importance of dominant species as drivers of diversity and ecosystem functioning, unravelling different dominance patterns is a research priority to direct conservation efforts in Amazonian forests
Understanding different dominance patterns in western Amazonian forests
Dominance of neotropical tree communities by a few species is widely documented, but dominant trees show a variety of distributional patterns still poorly understood. Here, we used 503 forest inventory plots (93,719 individuals â„2.5âcm diameter, 2609 species) to explore the relationships between local abundance, regional frequency and spatial aggregation of dominant species in four main habitat types in western Amazonia. Although the abundance-occupancy relationship is positive for the full dataset, we found that among dominant Amazonian tree species, there is a strong negative relationship between local abundance and regional frequency and/or spatial aggregation across habitat types. Our findings suggest an ecological trade-off whereby dominant species can be locally abundant (local dominants) or regionally widespread (widespread dominants), but rarely both (oligarchs). Given the importance of dominant species as drivers of diversity and ecosystem functioning, unravelling different dominance patterns is a research priority to direct conservation efforts in Amazonian forests.Publisher PDFPeer reviewe
Tree mode of death and mortality risk factors across Amazon forests
The carbon sink capacity of tropical forests is substantially affected by tree mortality. However, the main drivers of tropical tree death remain largely unknown. Here we present a pan-Amazonian assessment of how and why trees die, analysing over 120,000 trees representing > 3800 species from 189 long-term RAINFOR forest plots. While tree mortality rates vary greatly Amazon-wide, on average trees are as likely to die standing as they are broken or uprootedâmodes of death with different ecological consequences. Species-level growth rate is the single most important predictor of tree death in Amazonia, with faster-growing species being at higher risk. Within species, however, the slowest-growing trees are at greatest risk while the effect of tree size varies across the basin. In the driest Amazonian region species-level bioclimatic distributional patterns also predict the risk of death, suggesting that these forests are experiencing climatic conditions beyond their adaptative limits. These results provide not only a holistic pan-Amazonian picture of tree death but large-scale evidence for the overarching importance of the growthâsurvival trade-off in driving tropical tree mortality
The number of tree species on Earth
One of the most fundamental questions in ecology is how many species inhabit the Earth. However, due to massive logistical and financial challenges and taxonomic difficulties connected to the species concept definition, the global numbers of species, including those of important and well-studied life forms such as trees, still remain largely unknown. Here, based on global ground-sourced data, we estimate the total tree species richness at global, continental, and biome levels. Our results indicate that there are âŒ73,000 tree species globally, among which âŒ9,000 tree species are yet to be discovered. Roughly 40% of undiscovered tree species are in South America. Moreover, almost one-third of all tree species to be discovered may be rare, with very low populations and limited spatial distribution (likely in remote tropical lowlands and mountains). These findings highlight the vulnerability of global forest biodiversity to anthropogenic changes in land use and climate, which disproportionately threaten rare species and thus, global tree richness
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