8 research outputs found

    Author Correction: One sixth of Amazonian tree diversity is dependent on river floodplains

    Get PDF

    Mapping density, diversity and species-richness of the Amazon tree flora

    Get PDF
    Using 2.046 botanically-inventoried tree plots across the largest tropical forest on Earth, we mapped tree species-diversity and tree species-richness at 0.1-degree resolution, and investigated drivers for diversity and richness. Using only location, stratified by forest type, as predictor, our spatial model, to the best of our knowledge, provides the most accurate map of tree diversity in Amazonia to date, explaining approximately 70% of the tree diversity and species-richness. Large soil-forest combinations determine a significant percentage of the variation in tree species-richness and tree alpha-diversity in Amazonian forest-plots. We suggest that the size and fragmentation of these systems drive their large-scale diversity patterns and hence local diversity. A model not using location but cumulative water deficit, tree density, and temperature seasonality explains 47% of the tree species-richness in the terra-firme forest in Amazonia. Over large areas across Amazonia, residuals of this relationship are small and poorly spatially structured, suggesting that much of the residual variation may be local. The Guyana Shield area has consistently negative residuals, showing that this area has lower tree species-richness than expected by our models. We provide extensive plot meta-data, including tree density, tree alpha-diversity and tree species-richness results and gridded maps at 0.1-degree resolution

    Pervasive gaps in Amazonian ecological research

    Get PDF
    Biodiversity loss is one of the main challenges of our time, and attempts to address it require a clear understanding of how ecological communities respond to environmental change across time and space. While the increasing availability of global databases on ecological communities has advanced our knowledge of biodiversity sensitivity to environmental changes, vast areas of the tropics remain understudied. In the American tropics, Amazonia stands out as the world's most diverse rainforest and the primary source of Neotropical biodiversity, but it remains among the least known forests in America and is often underrepresented in biodiversity databases. To worsen this situation, human-induced modifications may eliminate pieces of the Amazon's biodiversity puzzle before we can use them to understand how ecological communities are responding. To increase generalization and applicability of biodiversity knowledge, it is thus crucial to reduce biases in ecological research, particularly in regions projected to face the most pronounced environmental changes. We integrate ecological community metadata of 7,694 sampling sites for multiple organism groups in a machine learning model framework to map the research probability across the Brazilian Amazonia, while identifying the region's vulnerability to environmental change. 15%–18% of the most neglected areas in ecological research are expected to experience severe climate or land use changes by 2050. This means that unless we take immediate action, we will not be able to establish their current status, much less monitor how it is changing and what is being lost

    Consistent patterns of common species across tropical tree communities

    Get PDF
    Trees structure the Earth’s most biodiverse ecosystem, tropical forests. The vast number of tree species presents a formidable challenge to understanding these forests, including their response to environmental change, as very little is known about most tropical tree species. A focus on the common species may circumvent this challenge. Here we investigate abundance patterns of common tree species using inventory data on 1,003,805 trees with trunk diameters of at least 10 cm across 1,568 locations1,2,3,4,5,6 in closed-canopy, structurally intact old-growth tropical forests in Africa, Amazonia and Southeast Asia. We estimate that 2.2%, 2.2% and 2.3% of species comprise 50% of the tropical trees in these regions, respectively. Extrapolating across all closed-canopy tropical forests, we estimate that just 1,053 species comprise half of Earth’s 800 billion tropical trees with trunk diameters of at least 10 cm. Despite differing biogeographic, climatic and anthropogenic histories7, we find notably consistent patterns of common species and species abundance distributions across the continents. This suggests that fundamental mechanisms of tree community assembly may apply to all tropical forests. Resampling analyses show that the most common species are likely to belong to a manageable list of known species, enabling targeted efforts to understand their ecology. Although they do not detract from the importance of rare species, our results open new opportunities to understand the world’s most diverse forests, including modelling their response to environmental change, by focusing on the common species that constitute the majority of their trees

    Modeling Drying Isotherms Using A Structure Transition Model

    No full text
    Drying introduces structural changes in the target material that modify its interaction with water. In this work, we developed a model based on star fruit drying that considered two forms of interaction with water. This model provided a very good fit to the experimental data and was applicable to drying of other products such as apple, barley, and coffee. This model yielded better fits for data reported in the literature than other models. These findings suggest that the model is applicable to a wide range of systems. © 2013 Copyright Taylor and Francis Group, LLC.31910081019Fellows, P., (2000) Food Processing Technology Principles and Practice, 2nd Ed, , CRC Press, Boca Raton, FLMao, S.W., Srzednicki, G., Driscoll, R.H., Modeling of drying of selected varieties of australian peanuts (2012) Drying Technology, 30 (16), pp. 1890-1895Neto, M.M., Robl, F., Netto, J.C., Intoxication by star fruit (Averrhoa carambola) in six dialysis patients? (Preliminary report) (1998) Nephrology Dialisis Transplantation, 13 (3), pp. 570-572Chang, J.M., Hwang, S.J., Kuo, H.T., Tsai, J.C., Guh, J.Y., Chen, H.C., Tsai, J.H., Lai, Y.H., Fatal outcome after ingestion of star fruit (Averrhoa carambola) in uremic patients (2000) American Journal of Kidney Diseases, 35 (2), pp. 189-193Provasi, M., Oliveira, C.E., Martino, M.C., Pessini, L.G., Bazotte, R.B., Cortez, D.A.G., Avaliação da toxicidade e do potencial antihiperglicemiante da Averrhoa carambola L. (Oxalidaceae) (2001) Acta Scientiarum, 23 (3), pp. 665-669Baldini, V.L.S., Draeta, I.S., Nomura, E.H., Avaliação bioquímica de carambola (Averrhoa carambola, L.) (1982) Coletânea do ITAL, 12, pp. 283-291Bispo, J.A.C., Bonafe, C.F.S., de Souza, V.B., Silva, J.B.A., Carvalho, G.B.M., Extending the kinetic solution of the classic Michaelis-Menten model of enzyme action (2011) Journal of Mathematical Chemistry, 49 (9), pp. 1976-1995Bispo, J.A.C., Bonafe, C.F.S., Koblitz, M.G.B., Silva, C.G.S., Souza, A.R., Substrate and enzyme concentration dependence of the Henri-Michaelis-Menten model probed by numerical simulation (2013) Journal of Mathematical Chemistry, 51, pp. 144-152Page, G., (1949) Factors Influencing the Maximum Rates of Air-Drying Shelled Corn in Thin Layers, , Purdue University, Lafayatte, INKarathanos, V.T., Determination of water content of dried fruits by drying kinetics (1999) Journal of Food Engineering, 39 (4), pp. 337-344Verma, L.R., Bucklin, R.A., Endan, J.B., Wratten, F.T., Effects of drying air parameters on rice drying models (1985) Transactions of the ASAE, 28 (1), pp. 296-301Chen, X.D., Lin, S.X.Q., Air drying of milk droplet under constant and time-dependent conditions (2005) AIChE Journal, 51 (6), pp. 1790-1799Putranto, A., Chen, X.D., Roasting of barley and coffee modeled using the lumped-reaction engineering approach (L-REA) (2012) Drying Technology, 30 (5), pp. 475-483Lin, S.X.Q., Chen, X.D., A model for drying of an aqueous lactose droplet using the reaction engineering approach (2006) Drying Technology, 24 (11), pp. 1329-1334Putranto, A., Chen, X.D., Modeling intermittent drying of wood under rapidly varying temperature and humidity conditions with the lumped reaction engineering approach (L-REA) (2012) Drying Technology, 30 (14), pp. 1658-1665O'Callagh, J.R., Menzies, D.J., Bailey, P.H., Digital simulation of agricultural drier performance (1971) Journal of Agricultural Engineering Research, 16 (3), pp. 223-244Baini, R., Langrish, T.A.G., Choosing an appropriate drying model for intermittent and continuous drying of bananas (2007) Journal of Food Engineering, 79 (1), pp. 330-343Xu, G., Weber, G., Dynamics and time-averaged chemical potential of proteins: importance in oligomer association (1982) Proceedings of the National Academy of Sciences of the United States of America, 79 (17), pp. 5268-5271Weber, G., Phenomenological description of the association of protein subunits subjected to conformational drift. Effects of dilution and of hydrostatic pressure (1986) Biochemistry, 25 (12), pp. 3626-3631Weber, G., (1992) Protein Interactions, , Chapman & Hall, New YorkBispo, J.A.C., Bonafe, C.F.S., Joekes, I., Martinez, E.A., Carvalho, G.B.M., Norberto, D.R., Entropy and volume change of dissociation in tobacco mosaic virus probed by high pressure (2012) Journal of Physical Chemistry B, 166, pp. 14817-14828Velic, D., Planinic, M., Tomas, S., Bilic, M., Influence of airflow velocity on kinetics of convection apple drying (2004) Journal of Food Engineering, 64 (1), pp. 97-102Henderson, S.M., Pabis, S., Grain drying theory: IV. The effect of air flow rate on the drying index (1962) Journal of Agricultural Engineering Research, 7 (1), pp. 85-89Claussen, I.C., Ustad, T.S., Strommen, I., Waide, P.M., Atmospheric freeze drying-A review (2007) Drying Technology, 25 (4-6), pp. 947-957Wolff, E., Gibert, H., Part 2. Modeling drying kinetics using adsorption isotherms (1990) Drying Technology, 8 (2), pp. 405-428. , Atmosphericfreeze-dryingJangam, S.V., Joshi, V.S., Mujumdar, A.S., Thorat, B.N., Studies on dehydration of sapota (Achras zapota) (2008) Drying Technology, 26 (3), pp. 369-377Sharaf-Eldeen, Y.I., Blaisdell, J.L., Hamdy, M.Y., A model for ear corn drying (1980) Transactions of the ASAE, 23 (5), pp. 1261-1265Monod, J., Wyman, J., Changeux, J.P., On the nature of allosteric transitions: A plausible model (1965) Journal of Molecular Biology, 12 (1), pp. 88-118Akanbi, C.T., Adeyemi, R.S., Ojo, A., Drying characteristics and sorption isotherm of tomato slices (2006) Journal of Food Engineering, 73 (2), pp. 157-163Fabra, M.J., Talens, P., Moraga, G., Martinez-Navarrete, N., Sorption isotherm and state diagram of grapefruit as a tool to improve product processing and stability (2009) Journal of Food Engineering, 93 (1), pp. 52-5

    Local hydrological conditions influence tree diversity and composition across the Amazon basin

    Get PDF
    Tree diversity and composition in Amazonia are known to be strongly determined by the water supplied by precipitation. Nevertheless, within the same climatic regime, water availability is modulated by local topography and soil characteristics (hereafter referred to as local hydrological conditions), varying from saturated and poorly drained to well-drained and potentially dry areas. While these conditions may be expected to influence species distribution, the impacts of local hydrological conditions on tree diversity and composition remain poorly understood at the whole Amazon basin scale. Using a dataset of 443 1-ha non-flooded forest plots distributed across the basin, we investigate how local hydrological conditions influence 1) tree alpha diversity, 2) the community-weighted wood density mean (CWM-wd) – a proxy for hydraulic resistance and 3) tree species composition. We find that the effect of local hydrological conditions on tree diversity depends on climate, being more evident in wetter forests, where diversity increases towards locations with well-drained soils. CWM-wd increased towards better drained soils in Southern and Western Amazonia. Tree species composition changed along local soil hydrological gradients in Central-Eastern, Western and Southern Amazonia, and those changes were correlated with changes in the mean wood density of plots. Our results suggest that local hydrological gradients filter species, influencing the diversity and composition of Amazonian forests. Overall, this study shows that the effect of local hydrological conditions is pervasive, extending over wide Amazonian regions, and reinforces the importance of accounting for local topography and hydrology to better understand the likely response and resilience of forests to increased frequency of extreme climate events and rising temperatures

    One sixth of Amazonian tree diversity is dependent on river floodplains

    Get PDF
    Amazonia’s floodplain system is the largest and most biodiverse on Earth. Although forests are crucial to the ecological integrity of floodplains, our understanding of their species composition and how this may differ from surrounding forest types is still far too limited, particularly as changing inundation regimes begin to reshape floodplain tree communities and the critical ecosystem functions they underpin. Here we address this gap by taking a spatially explicit look at Amazonia-wide patterns of tree-species turnover and ecological specialization of the region’s floodplain forests. We show that the majority of Amazonian tree species can inhabit floodplains, and about a sixth of Amazonian tree diversity is ecologically specialized on floodplains. The degree of specialization in floodplain communities is driven by regional flood patterns, with the most compositionally differentiated floodplain forests located centrally within the fluvial network and contingent on the most extraordinary flood magnitudes regionally. Our results provide a spatially explicit view of ecological specialization of floodplain forest communities and expose the need for whole-basin hydrological integrity to protect the Amazon’s tree diversity and its function

    The biogeography of the Amazonian tree flora

    Get PDF
    We describe the geographical variation in tree species composition across Amazonian forests and show how environmental conditions are associated with species turnover. Our analyses are based on 2023 forest inventory plots (1 ha) that provide abundance data for a total of 5188 tree species. Within-plot species composition reflected both local environmental conditions (especially soil nutrients and hydrology) and geographical regions. A broader-scale view of species turnover was obtained by interpolating the relative tree species abundances over Amazonia into 47,441 0.1-degree grid cells. Two main dimensions of spatial change in tree species composition were identified. The first was a gradient between western Amazonia at the Andean forelands (with young geology and relatively nutrient-rich soils) and central–eastern Amazonia associated with the Guiana and Brazilian Shields (with more ancient geology and poor soils). The second gradient was between the wet forests of the northwest and the drier forests in southern Amazonia. Isolines linking cells of similar composition crossed major Amazonian rivers, suggesting that tree species distributions are not limited by rivers. Even though some areas of relatively sharp species turnover were identified, mostly the tree species composition changed gradually over large extents, which does not support delimiting clear discrete biogeographic regions within Amazonia
    corecore