77 research outputs found

    Representatividad a escala regional de un inventario florĂ­stico detallado de una hectĂĄrea en los andes tropicales

    Get PDF
    Floristic composition of vascular plants and their distribution is reported for growth habits in a low montane rain forest (2600 m and 2500 mm/yr mean annual precipitation) in the northern Andes, based on a plot of 1 ha. The samples collected represented 318 species/morphospecies, 82 families (nine of which were pteridophytes) and 173 genera. 78% of the samples were identified to species. Groups with most species are pteridophytes (sensu lato), Orchidaceae, Asteraceae, Rubiaceae, Melastomataceae and Piperaceae, that represented 44% of all species recorded. The most diverse genera arePeperomia, Elaphoglossum, Mikania, Anthurium, and Miconia. Three species endemic to Antioquia (Brunellia trianae, Meriania antioquiensis and Mikania fragrans) were found. The individuals found in the plot represent 47% of the species, 48% of the genera and 60% of the families found in ArvĂ­ Park, a reserve of 11400 hectares in which the plot was located. The plot had 108 species, 30 genera and one family not previously reported for Arvi Park. The number of common taxa between the plot and the ArvĂ­ Park was 144 species, 142 genera and 69 families. Species richness/family in the plot accounts for 89% of the variation of species richness/family in the ArvĂ­ Park, and 75% of the generic richness. We conclude that detailed floristic inventory of known area plots provide information representative of the regional flora and permit a rapid approximation of its biodiversity.Se reporta la composiciĂłn florĂ­stica de plantas vasculares y su distribuciĂłn por hĂĄbitos de crecimiento en un bosque hĂșmedo montano bajo en el norte de los Andes, con base en una parcela de 1 ha. Dentro de la parcela de 1 ha se colectaron muestras botĂĄnicas de manera intensiva y se identificaron 318 especies/morfoespecies, 82 familias (9 de las cuales pertenecen a la divisiĂłn Pteridophyta) y 173 gĂ©neros. Orchidaceae, Asteraceae, Rubiaceae, Melastomataceae y Piperaceae aportan el 44% del total de especies registradas en la parcela. Los gĂ©neros mĂĄs diversos sonPeperomia, Elaphoglossum, Mikania, Anthurium y Miconia. Se encontraron tres especies endĂ©micas del departamento de Antioquia (Brunellia trianae, Meriania antioquiensis y Mikania fragrans). Las especies encontradas representan el 47%, los gĂ©neros el 48% y las familias el 60% del total con respecto al Parque ArvĂ­, una reserva de 11 400 ha donde se localizĂł la parcela. Se encontraron 108 especies, 30 gĂ©neros y 1 familia no reportados previamente para el Parque ArvĂ­. El nĂșmero de taxones comunes entre la parcela y el Parque fue de 144 especies, 142 gĂ©neros y 69 familias. La riqueza de especies/familia en la parcela explica el 89% de la variaciĂłn en la riqueza de especies/familia en al Parque ArvĂ­, y la riqueza de gĂ©neros el 75%. Se concluye que los inventarios florĂ­sticos detallados en parcelas de ĂĄrea conocida aportan informaciĂłn representativa de la flora a nivel regional y permiten una aproximaciĂłn rĂĄpida a su biodiversidad

    Regional and seasonal patterns of litterfall in tropical South America

    Get PDF
    The production of aboveground soft tissue represents an important share of total net primary production in tropical rain forests. Here we draw from a large number of published and unpublished datasets (n=81 sites) to assess the determinants of litterfall variation across South American tropical forests. We show that across old-growth tropical rainforests, litterfall averages 8.61±1.91 Mg ha−1 yr−1 (mean ± standard deviation, in dry mass units). Secondary forests have a lower annual litterfall than old-growth tropical forests with a mean of 8.01±3.41 Mg ha−1 yr−1. Annual litterfall shows no significant variation with total annual rainfall, either globally or within forest types. It does not vary consistently with soil type, except in the poorest soils (white sand soils), where litterfall is significantly lower than in other soil types (5.42±1.91 Mg ha−1 yr−1). We also study the determinants of litterfall seasonality, and find that it does not depend on annual rainfall or on soil type. However, litterfall seasonality is significantly positively correlated with rainfall seasonality. Finally, we assess how much carbon is stored in reproductive organs relative to photosynthetic organs. Mean leaf fall is 5.74±1.83 Mg ha−1 yr−1 (71% of total litterfall). Mean allocation into reproductive organs is 0.69±0.40 Mg ha−1 yr−1 (9% of total litterfall). The investment into reproductive organs divided by leaf litterfall increases with soil fertility, suggesting that on poor soils, the allocation to photosynthetic organs is prioritized over that to reproduction. Finally, we discuss the ecological and biogeochemical implications of these result

    Evenness mediates the global relationship between forest productivity and richness

    Get PDF
    1. Biodiversity is an important component of natural ecosystems, with higher species richness often correlating with an increase in ecosystem productivity. Yet, this relationship varies substantially across environments, typically becoming less pronounced at high levels of species richness. However, species richness alone cannot reflect all important properties of a community, including community evenness, which may mediate the relationship between biodiversity and productivity. If the evenness of a community correlates negatively with richness across forests globally, then a greater number of species may not always increase overall diversity and productivity of the system. Theoretical work and local empirical studies have shown that the effect of evenness on ecosystem functioning may be especially strong at high richness levels, yet the consistency of this remains untested at a global scale.2. Here, we used a dataset of forests from across the globe, which includes composition, biomass accumulation and net primary productivity, to explore whether productivity correlates with community evenness and richness in a way that evenness appears to buffer the effect of richness. Specifically, we evaluated whether low levels of evenness in speciose communities correlate with the attenuation of the richness–productivity relationship.3. We found that tree species richness and evenness are negatively correlated across forests globally, with highly speciose forests typically comprising a few dominant and many rare species. Furthermore, we found that the correlation between diversity and productivity changes with evenness: at low richness, uneven communities are more productive, while at high richness, even communities are more productive.4. Synthesis. Collectively, these results demonstrate that evenness is an integral component of the relationship between biodiversity and productivity, and that the attenuating effect of richness on forest productivity might be partly explained by low evenness in speciose communities. Productivity generally increases with species richness, until reduced evenness limits the overall increases in community diversity. Our research suggests that evenness is a fundamental component of biodiversity–ecosystem function relationships, and is of critical importance for guiding conservation and sustainable ecosystem management decisions

    Global patterns and environmental drivers of forest functional composition

    Get PDF
    To determine the relationships between the functional trait composition of forest communities and environmental gradients across scales and biomes and the role of species relative abundances in these relationships. We integrated species abundance records from worldwide forest inventories and associated functional traits (wood density, specific leaf area and seed mass) to obtain a data set of 99,953 to 149,285 plots (depending on the trait) spanning all forested continents. We computed community-weighted and unweighted means of trait values for each plot and related them to three broad environmental gradients and their interactions (energy availability, precipitation and soil properties) at two scales (global and biomes). Our models explained up to 60% of the variance in trait distribution. At global scale, the energy gradient had the strongest influence on traits. However, withinbiome models revealed different relationships among biomes. Notably, the functional composition of tropical forests was more influenced by precipitation and soil properties than energy availability, whereas temperate forests showed the opposite pattern. Depending on the trait studied, response to gradients was more variable and proportionally weaker in boreal forests. Community unweighted means were better predicted than weighted means for almost all models. Worldwide, trees require a large amount of energy (following latitude) to produce dense wood and seeds, while leaves with large surface to weight ratios are concentrated in temperate forests. However, patterns of functional composition within-biome differ from global patterns due to biome specificities such as the presence of conifers or unique combinations of climatic and soil properties. We recommend assessing the sensitivity of tree functional traits to environmental changes in their geographic context. Furthermore, at a given site, the distribution of tree functional traits appears to be driven more by species presence than species abundance.Fil: Bouchard, Elise. UniversitĂ© du QuĂ©bec a Montreal; CanadĂĄFil: Searle, Eric B.. UniversitĂ© du QuĂ©bec a Montreal; CanadĂĄFil: Drapeau, Pierre. UniversitĂ© du QuĂ©bec a Montreal; CanadĂĄFil: Liang, Jingjing. Purdue University; Estados UnidosFil: Gamarra, Javier G. P.. Food and Agriculture Organization of the United Nations; ItaliaFil: Abegg, Meinrad. No especifĂ­ca;Fil: Alberti, Giorgio. No especifĂ­ca;Fil: Zambrano, Angelica Almeyda. No especifĂ­ca;Fil: Alvarez Davila, Esteban. No especifĂ­ca;Fil: Alves, Luciana F.. No especifĂ­ca;Fil: Avitabile, Valerio. No especifĂ­ca;Fil: Aymard, Gerardo. No especifĂ­ca;Fil: Bastin, Jean François. No especifĂ­ca;Fil: Birnbaum, Philippe. No especifĂ­ca;Fil: Bongers, Frans. No especifĂ­ca;Fil: Bouriaud, Olivier. No especifĂ­ca;Fil: Brancalion, Pedro. No especifĂ­ca;Fil: Broadbent, Eben. No especifĂ­ca;Fil: Bussotti, Filippo. No especifĂ­ca;Fil: Gatti, Roberto Cazzolla. No especifĂ­ca;Fil: ČeĆĄljar, Goran. No especifĂ­ca;Fil: Chisholm, Chelsea. No especifĂ­ca;Fil: Cienciala, Emil. No especifĂ­ca;Fil: Clark, Connie J.. No especifĂ­ca;Fil: Peri, Pablo Luis. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas. Centro de Investigaciones y Transferencia de Santa Cruz. Universidad TecnolĂłgica Nacional. Facultad Regional Santa Cruz. Centro de Investigaciones y Transferencia de Santa Cruz. Universidad Nacional de la Patagonia Austral. Centro de Investigaciones y Transferencia de Santa Cruz; ArgentinaFil: ZawiƂa NiedĆșwiecki, Tomasz. No especifĂ­ca;Fil: Zhou, Mo. No especifĂ­ca;Fil: Zhu, Zhi Xin. No especifĂ­ca;Fil: Zo Bi, IriĂ© C.. No especifĂ­ca;Fil: Paquette, Alain. UniversitĂ© du QuĂ©bec a Montreal; Canad

    The number of tree species on Earth

    Get PDF
    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 ∌73,000 tree species globally, among which ∌9,000 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

    Regional and large-scale patterns in Amazon forest structure and function are mediated by variations in soil physical and chemical properties

    Get PDF
    Forest structure and dynamics have been noted to vary across the Amazon Basin in an east-west gradient in a pattern which coincides with variations in soil fertility and geology. This has resulted in the hypothesis that soil fertility may play an important role in explaining Basin-wide variations in forest biomass, growth and stem turnover rates. To test this hypothesis and assess the importance of edaphic properties in affect forest structure and dynamics, soil and plant samples were collected in a total of 59 different forest plots across the Amazon Basin. Samples were analysed for exchangeable cations, C, N, pH with various Pfractions also determined. Physical properties were also examined and an index of soil physical quality developed. Overall, forest structure and dynamics were found to be strongly and quantitatively related to edaphic conditions. Tree turnover rates emerged to be mostly influenced by soil physical properties whereas forest growth rates were mainly related to a measure of available soil phosphorus, although also dependent on rainfall amount and distribution. On the other hand, large scale variations in forest biomass could not be explained by any of the edaphic properties measured, nor by variation in climate. A new hypothesis of self-maintaining forest dynamic feedback mechanisms initiated by edaphic conditions is proposed. It is further suggested that this is a major factor determining forest disturbance levels, species composition and forest productivity on a Basin wide scale

    Evenness mediates the global relationship between forest productivity and richness

    Get PDF
    1. Biodiversity is an important component of natural ecosystems, with higher species richness often correlating with an increase in ecosystem productivity. Yet, this relationship varies substantially across environments, typically becoming less pronounced at high levels of species richness. However, species richness alone cannot reflect all important properties of a community, including community evenness, which may mediate the relationship between biodiversity and productivity. If the evenness of a community correlates negatively with richness across forests globally, then a greater number of species may not always increase overall diversity and productivity of the system. Theoretical work and local empirical studies have shown that the effect of evenness on ecosystem functioning may be especially strong at high richness levels, yet the consistency of this remains untested at a global scale. 2. Here, we used a dataset of forests from across the globe, which includes composition, biomass accumulation and net primary productivity, to explore whether productivity correlates with community evenness and richness in a way that evenness appears to buffer the effect of richness. Specifically, we evaluated whether low levels of evenness in speciose communities correlate with the attenuation of the richness–productivity relationship. 3. We found that tree species richness and evenness are negatively correlated across forests globally, with highly speciose forests typically comprising a few dominant and many rare species. Furthermore, we found that the correlation between diversity and productivity changes with evenness: at low richness, uneven communities are more productive, while at high richness, even communities are more productive. 4. Synthesis. Collectively, these results demonstrate that evenness is an integral component of the relationship between biodiversity and productivity, and that the attenuating effect of richness on forest productivity might be partly explained by low evenness in speciose communities. Productivity generally increases with species richness, until reduced evenness limits the overall increases in community diversity. Our research suggests that evenness is a fundamental component of biodiversity– ecosystem function relationships, and is of critical importance for guiding conservation and sustainable ecosystem management decisions

    The number of tree species on Earth

    Get PDF
    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 ∌73,000 tree species globally, among which ∌9,000 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. Please note an (erratum/corrigendum) for this article is available via https://www.pnas.org/doi/10.1073/pnas.220278411

    Aboveground forest biomass varies across continents, ecological zones and successional stages: refined IPCC default values for tropical and subtropical forests

    Get PDF
    For monitoring and reporting forest carbon stocks and fluxes, many countries in the tropics and subtropics rely on default values of forest aboveground biomass (AGB) from the Intergovernmental Panel on Climate Change (IPCC) guidelines for National Greenhouse Gas (GHG) Inventories. Default IPCC forest AGB values originated from 2006, and are relatively crude estimates of average values per continent and ecological zone. The 2006 default values were based on limited plot data available at the time, methods for their derivation were not fully clear, and no distinction between successional stages was made. As part of the 2019 Refinement to the 2006 IPCC Guidelines for GHG Inventories, we updated the default AGB values for tropical and subtropical forests based on AGB data from >25 000 plots in natural forests and a global AGB map where no plot data were available. We calculated refined AGB default values per continent, ecological zone, and successional stage, and provided a measure of uncertainty. AGB in tropical and subtropical forests varies by an order of magnitude across continents, ecological zones, and successional stage. Our refined default values generally reflect the climatic gradients in the tropics, with more AGB in wetter areas. AGB is generally higher in old-growth than in secondary forests, and higher in older secondary (regrowth >20 years old and degraded/logged forests) than in young secondary forests (20 years old). While refined default values for tropical old-growth forest are largely similar to the previous 2006 default values, the new default values are 4.0-7.7-fold lower for young secondary forests. Thus, the refined values will strongly alter estimated carbon stocks and fluxes, and emphasize the critical importance of old-growth forest conservation. We provide a reproducible approach to facilitate future refinements and encourage targeted efforts to establish permanent plots in areas with data gaps

    Variation in stem mortality rates determines patterns of above-ground biomass in Amazonian forests: implications for dynamic global vegetation models

    Get PDF
    Understanding the processes that determine above-ground biomass (AGB) in Amazonian forests is important for predicting the sensitivity of these ecosystems to environmental change and for designing and evaluating dynamic global vegetation models (DGVMs). AGB is determined by inputs from woody productivity [woody net primary productivity (NPP)] and the rate at which carbon is lost through tree mortality. Here, we test whether two direct metrics of tree mortality (the absolute rate of woody biomass loss and the rate of stem mortality) and/or woody NPP, control variation in AGB among 167 plots in intact forest across Amazonia. We then compare these relationships and the observed variation in AGB and woody NPP with the predictions of four DGVMs. The observations show that stem mortality rates, rather than absolute rates of woody biomass loss, are the most important predictor of AGB, which is consistent with the importance of stand size structure for determining spatial variation in AGB. The relationship between stem mortality rates and AGB varies among different regions of Amazonia, indicating that variation in wood density and height/diameter relationships also influences AGB. In contrast to previous findings, we find that woody NPP is not correlated with stem mortality rates and is weakly positively correlated with AGB. Across the four models, basin-wide average AGB is similar to the mean of the observations. However, the models consistently overestimate woody NPP and poorly represent the spatial patterns of both AGB and woody NPP estimated using plot data. In marked contrast to the observations, DGVMs typically show strong positive relationships between woody NPP and AGB. Resolving these differences will require incorporating forest size structure, mechanistic models of stem mortality and variation in functional composition in DGVMs
    • 

    corecore