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Talaga, S.; Dezerald, O.; Carteron, A.; Petitclerc, F.; Leroy, C.; Céréghino, R.; Dejean, A. |
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Tank bromeliads as natural microcosms: A facultative association with ants influences the aquatic invertebrate community structure |
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Journal Article |
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2015 |
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Comptes Rendus – Biologies |
Abbreviated Journal |
Comptes Rendus – Biologies |
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338 |
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10 |
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696-700 |
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Aechmea; Ant-bromeliad associations; Aquatic communities; Odontomachus; Phytotelm |
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Many tank bromeliads have facultative relationships with ants as is the case in French Guiana between Aechmea aquilega (Salib.) Griseb. and the trap-jaw ant, Odontomachus haematodus Linnaeus. Using a redundancy analysis, we determined that the presence of O. haematodus colonies is accompanied by a greater quantity of fine particulate organic matter in the water likely due to their wastes. This increase in nutrient availability is significantly correlated with an increase in the abundance of some detritivorous taxa, suggesting a positive bottom-up influence on the aquatic macroinvertebrate communities living in the A. aquilega wells. On the other hand, the abundance of top predators is negatively affected by a lower number of available wells due to ant constructions for nesting, releasing a top-down pressure that could also favor lower trophic levels. © 2015 Académie des sciences. |
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CNRS, Ecolab (UMR-CNRS 5245), 118, route de Narbonne, Toulouse, France |
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Export Date: 2 October 2015 |
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EcoFoG @ webmaster @ |
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627 |
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Fayad, I.; Baghdadi, N.; Guitet, S.; Bailly, J.-S.; Herault, B.; Gond, V.; El Hajj, M.; Tong Minh, D.H. |
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Aboveground biomass mapping in French Guiana by combining remote sensing, forest inventories and environmental data |
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Journal Article |
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2016 |
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International Journal of Applied Earth Observation and Geoinformation |
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International Journal of Applied Earth Observation and Geoinformation |
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52 |
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502-514 |
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Aboveground biomass mapping; Forests; French Guiana; ICESat GLAS; LiDAR |
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Mapping forest aboveground biomass (AGB) has become an important task, particularly for the reporting of carbon stocks and changes. AGB can be mapped using synthetic aperture radar data (SAR) or passive optical data. However, these data are insensitive to high AGB levels (>150 Mg/ha, and >300 Mg/ha for P-band), which are commonly found in tropical forests. Studies have mapped the rough variations in AGB by combining optical and environmental data at regional and global scales. Nevertheless, these maps cannot represent local variations in AGB in tropical forests. In this paper, we hypothesize that the problem of misrepresenting local variations in AGB and AGB estimation with good precision occurs because of both methodological limits (signal saturation or dilution bias) and a lack of adequate calibration data in this range of AGB values. We test this hypothesis by developing a calibrated regression model to predict variations in high AGB values (mean >300 Mg/ha) in French Guiana by a methodological approach for spatial extrapolation with data from the optical geoscience laser altimeter system (GLAS), forest inventories, radar, optics, and environmental variables for spatial inter- and extrapolation. Given their higher point count, GLAS data allow a wider coverage of AGB values. We find that the metrics from GLAS footprints are correlated with field AGB estimations (R2 = 0.54, RMSE = 48.3 Mg/ha) with no bias for high values. First, predictive models, including remote-sensing, environmental variables and spatial correlation functions, allow us to obtain “wall-to-wall” AGB maps over French Guiana with an RMSE for the in situ AGB estimates of ∼50 Mg/ha and R2 = 0.66 at a 1-km grid size. We conclude that a calibrated regression model based on GLAS with dependent environmental data can produce good AGB predictions even for high AGB values if the calibration data fit the AGB range. We also demonstrate that small temporal and spatial mismatches between field data and GLAS footprints are not a problem for regional and global calibrated regression models because field data aim to predict large and deep tendencies in AGB variations from environmental gradients and do not aim to represent high but stochastic and temporally limited variations from forest dynamics. Thus, we advocate including a greater variety of data, even if less precise and shifted, to better represent high AGB values in global models and to improve the fitting of these models for high values. © 2016 Elsevier B.V. |
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NOVELTIS, 153 rue du Lac, Labège, France |
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Export Date: 9 December 2016 |
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EcoFoG @ webmaster @ |
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699 |
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Mortier, F.; Rossi, V.; Guillot, G.; Gourlet-Fleury, S.; Picard, N. |
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Population dynamics of species-rich ecosystems: The mixture of matrix population models approach |
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2013 |
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Methods in Ecology and Evolution |
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Methods Ecol. Evol. |
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4 |
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4 |
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316-326 |
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Bayesian; Clustering; Mixture models; Population dynamics; Reversible jump Markov chain Monte Carlo; Species-rich ecosystems; Tropical rain forests |
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Matrix population models are widely used to predict population dynamics, but when applied to species-rich ecosystems with many rare species, the small population sample sizes hinder a good fit of species-specific models. This issue can be overcome by assigning species to groups to increase the size of the calibration data sets. However, the species classification is often disconnected from the matrix modelling and from the estimation of matrix parameters, thus bringing species groups that may not be optimal with respect to the predicted community dynamics. We proposed here a method that jointly classified species into groups and fit the matrix models in an integrated way. The model was a special case of mixture with unknown number of components and was cast in a Bayesian framework. An MCMC algorithm was developed to infer the unknown parameters: the number of groups, the group of each species and the dynamics parameters. We applied the method to simulated data and showed that the algorithm efficiently recovered the model parameters. We applied the method to a data set from a tropical rain forest in French Guiana. The mixture matrix model classified tree species into well-differentiated groups with clear ecological interpretations. It also accurately predicted the forest dynamics over the 16-year observation period. Our model and algorithm can straightforwardly be adapted to any type of matrix model, using the life cycle diagram. It can be used as an unsupervised classification technique to group species with similar population dynamics. © 2012 The Authors. Methods in Ecology and Evolution © 2012 British Ecological Society. |
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Statistics Section IMM, Technical University of Denmark, Copenhagen, Denmark |
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2041210x (Issn) |
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Export Date: 16 April 2013; Source: Scopus; :doi 10.1111/2041-210x.12019; Language of Original Document: English; Correspondence Address: Mortier, F.; CIRAD, UPR Bsef, Montpellier, 34398, France; email: frederic.mortier@cirad.fr |
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EcoFoG @ webmaster @ |
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480 |
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Marcon, E. |
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Entropy as a common measure of biodiversity and the spatial structure of economic activity |
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2019 |
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Revue Economique |
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Rev. Econ. |
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70 |
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3 |
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305-326 |
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Diversity; Economic geography; Spatial concentration; Specialization |
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Measures of spatial concentration and specialization in economics are similar to those of biodiversity and ubiquity of species in ecology. Entropy is the fundamental tool that originated in statistical physics and information theory. The definition of number equivalents or effective numbers, that is the number of types in an ideal, simplified distribution, is introduced along with the partitioning of the joint diversity of a bi-dimensional distribution into absolute and relative concentration or specialization and replication. The whole framework is theoretically robust and allows measuring the spatial structure of a discrete space. |
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AgroParisTech, UMR Écologie des forêts de Guyane, CNRS, Cirad, INRA, Université des Antilles, Université de Guyane, Campus Agronomique, BP 701, Kourou, 97310, French Guiana |
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Presses de Sciences Po |
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00352764 (Issn) |
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EcoFoG @ webmaster @ |
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912 |
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Marcon, E.; Herault, B. |
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Decomposing phylodiversity |
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2015 |
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Methods in Ecology and Evolution |
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Methods in Ecology and Evolution |
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6 |
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3 |
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333-339 |
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Biodiversity; Entropy; Functional diversity; Phylogenetic diversity |
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Measuring functional or phylogenetic diversity is the object of an active literature. The main issues to address are relating measures to a clear conceptual framework, allowing unavoidable estimation-bias correction and decomposing diversity along spatial scales. We provide a general mathematical framework to decompose measures of species-neutral, phylogenetic or functional diversity into α and β components. We first unify the definitions of phylogenetic and functional entropy and diversity as a generalization of HCDT entropy and Hill numbers when an ultrametric tree is considered. We then derive the decomposition of diversity. We propose a bias correction of the estimates allowing meaningful computation from real, often undersampled communities. Entropy can be transformed into true diversity, that is an effective number of species or communities. Estimators of α- and β-entropy, phylogenetic and functional entropy are provided. Proper definition and estimation of diversity is the first step towards better understanding its underlying ecological and evolutionary mechanisms. © 2015 British Ecological Society. |
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Cirad, UMR EcoFoG, BP 709Kourou, French Guiana |
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Export Date: 31 March 2015 |
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EcoFoG @ webmaster @ |
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590 |
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Courtois, E. A.; Stahl, C.; Burban, B.; Van Den Berge, J.; Berveiller, D.; Bréchet, L.; Larned Soong, J.; Arriga, N.; Peñuelas, J.; August Janssens, I. |
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Automatic high-frequency measurements of full soil greenhouse gas fluxes in a tropical forest |
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2019 |
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Biogeosciences |
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Biogeosciences |
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16 |
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3 |
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785-796 |
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Measuring in situ soil fluxes of carbon dioxide (CO 2 ), methane (CH 4 ), and nitrous oxide (N 2 O) continuously at high frequency requires appropriate technology. We tested the combination of a commercial automated soil CO 2 flux chamber system (LI-8100A) with a CH 4 and N 2 O analyzer (Picarro G2308) in a tropical rainforest for 4 months. A chamber closure time of 2 min was sufficient for a reliable estimation of CO 2 and CH 4 fluxes (100% and 98.5% of fluxes were above minimum detectable flux – MDF, respectively). This closure time was generally not suitable for a reliable estimation of the low N 2 O fluxes in this ecosystem but was sufficient for detecting rare major peak events. A closure time of 25 min was more appropriate for reliable estimation of most N 2 O fluxes (85.6% of measured fluxes are above MDF±0.002 nmolm -2 s -1 ). Our study highlights the importance of adjusted closure time for each gas. © Author(s) 2019. |
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CREAF, Cerdanyola Del Vallès, Catalonia, 08193, Spain |
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Copernicus GmbH |
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Export Date: 25 February 2019; Correspondence Address: Alice Courtois, E.; Department of Biology University of Antwerp, Centers of Excellence Global Change Ecology and PLECO (Plants and Ecosystems), Universiteitsplein 1, Belgium; email: courtoiselodie@gmail.com; Funding details: Centre de Coopération Internationale en Recherche Agronomique pour le Développement, CIRAD; Funding details: European Research Council, ERC, ERC-2013-SyG 610028-IMBALANCE-P; Funding details: ANR-10-LABX-25-01, ANR-11-INBS-0001; Funding details: U.S. Department of Energy, DOE, DE-AC02-05CH11231; Funding details: Agence Nationale de la Recherche, ANR; Funding details: Institut National de la Recherche Agronomique, INRA; Funding details: Fonds Wetenschappelijk Onderzoek, FWO; Funding text 1: Acknowledgements. This research was supported by the European Research Council Synergy grant ERC-2013-SyG 610028-IMBALANCE-P. We thank Jan Segers for help in the initial setting of the system and Renato Winkler from Picarro and Rod Madsen and Jason Hupp from LI-COR for their help in combining the systems. We thank the staff of Paracou station, managed by UMR Ecofog (CIRAD, INRA; Kourou), which received support from “Investissement d’Avenir” grants managed by Agence Nationale de la Recherche (CEBA: ANR-10-LABX-25-01, ANAEE-France: ANR-11-INBS-0001). This study was conducted in collaboration with the Guyaflux program belonging to SOERE F-ORE-T, which is supported annually by Ecofor, Allenvi, and the French national research infrastructure, ANAEE-F. This program also received support from an “investissement d’avenir” grant from the Agence Nationale de la Recherche (CEBA, ref ANR-10-LABX-25-01). Ivan August Janssens acknowledges support from Antwerp University (Methusalem funding), Nicola Arriga from ICOS-Belgium and Fonds Wetenschappelijk Onderzoek (FWO), and Jennifer Larned Soong from the U.S. Department of Energy under contract DE-AC02-05CH11231.; References: Aguilos, M., Hérault, B., Burban, B., Wagner, F., Bonal, D., What drives long-Term variations in carbon flux and balance in a tropical rainforest in French Guiana? (2018) Agr. Forest Meteorol, 253, pp. 114-123; Ambus, P., Skiba, U., Drewer, J., Jones, S., Carter, M.S., Albert, K.R., Sutton, M., Development of an accumulation-based system for cost-effective chamber measurements of inert trace gas fluxes (2010) Eur. J. Soil Sci, 61, pp. 785-792; Arias-Navarro, C., Díaz-Pinés, E., Klatt, S., Brandt, P., Rufino, M.C., Butterbach-Bahl, K., Verchot, L., Spatial variability of soil N2O and CO2 fluxes in different topographic positions in a tropical montane forest in Kenya (2017) J. Geophys. Res.-Biogeo, 122, pp. 514-527; Bonal, D., Bosc, A., Ponton, S., Goret, J.Y., Burban, B., Gross, P., Bonnefond, J., Epron, D., Impact of severe dry season on net ecosystem exchange in the Neotropical rainforest of French Guiana (2008) Glob. Change Biol, 14, pp. 1917-1933; Bréchet, L., Ponton, S., Roy, J., Freycon, V., Coteaux, M.-M., Bonal, D., Epron, D., Do tree species characteristics influence soil respiration in tropical forests? A test based on 16 tree species planted in monospecific plots (2009) Plant Soil, 319, pp. 235-246; Breuer, L., Papen, H., Butterbach-Bahl, K., N2O emission from tropical forest soils of Australia (2000) J. Geophys. Res.-Atmos, 105, pp. 26353-26367; Christiansen, J.R., Outhwaite, J., Smukler, S.M., Comparison of CO2, CH4 and N2O soil-Atmosphere exchange measured in static chambers with cavity ring-down spectroscopy and gas chromatography (2015) Agr. Forest Meteorol, 211, pp. 48-57; Courtois, E.A., Stahl, C., Dataset from Automatic high-frequency measurements of full soil greenhouse gas fluxes in a tropical forest (2019) Biogeosciences, 2019. , https://doi.org/10.5281/zenodo.2555299; Courtois, E.A., Stahl, C., Van Den Berge, J., Bréchet, L., Van Langenhove, L., Richter, A., Urbina, I., Janssens, I.A., Spatial variation of soil CO2, CH4 and N2O fluxes across topographical positions in tropical forests of the Guiana Shield (2018) Ecosystems, 21, pp. 1445-1458; Davidson, E., Savage, K., Verchot, L., Navarro, R., Minimizing artifacts and biases in chamber-based measurements of soil respiration (2002) Agr. Forest Meteorol, 113, pp. 21-37; Davidson, E.A., Nepstad, D.C., Ishida, F.Y., Brando, P.M., Effects of an experimental drought and recovery on soil emissions of carbon dioxide, methane, nitrous oxide, and nitric oxide in a moist tropical forest (2008) Glob. Change Biol, 14, pp. 2582-2590; De Klein, C., Harvey, M., (2012) Nitrous Oxide Chamber Methodology Guidelines, , Ministry for Primary Industries, Wellington, New Zealand; Denmead, O., Chamber systems for measuring nitrous oxide emission from soils in the field (1979) Soil Sci. Soc. Am. J, 43, pp. 89-95; Dutaur, L., Verchot, L.V., A global inventory of the soil CH4 sink (2007) Glob. Biogeochem. Cy, p. 21. , https://doi.org/10.1029/2006GB002734; Epron, D., Bosc, A., Bonal, D., Freycon, V., Spatial variation of soil respiration across a topographic gradient in a tropical rain forest in French Guiana (2006) J. Trop. Ecol, 22, pp. 565-574; (1998) World Reference Base for Soil Resources, , FAO/ ISRIC/ISSS.FAO, ISRIC, ISSS, World Soil Resources Reports 84, Rome; Görres, C.-M., Kammann, C., Ceulemans, R., Automation of soil flux chamber measurements, potentials and pitfalls (2016) Biogeosciences, 13, pp. 1949-1966. , https://doi.org/10.5194/bg-13-1949-2016; Hupp, J.R., Garcia, R.L., Madsen, R., McDermitt, D.K., Measurement of CO2 evolution in a multiplexed flask system (2009) Amer. Soc. Horticultural Science, Alexandria USA, 44, pp. 1143-1143; Janssens, I.A., Kowalski, A.S., Longdoz, B., Ceulemans, R., Assessing forest soil CO2 efflux, an in-situ comparison of four techniques (2000) Tree Physiol, 20, pp. 23-32; Koskinen, M., Minkkinen, K., Ojanen, P., Kämäräinen, M., Laurila, T., Lohila, A., Measurements of CO2 exchange with an automated chamber system throughout the year, challenges in measuring night-Time respiration on porous peat soil (2014) Biogeosciences, 11, pp. 347-363. , https://doi.org/10.5194/bg-11-347-2014; Kostyanovsky, K., Huggins, D., Stockle, C., Waldo, S., Lamb, B., Developing a flow through chamber system for automated measurements of soil N2O and CO2 emissions (2018) Measurement, 113, pp. 172-180; Merbold, L., Wohlfahrt, G., Butterbach-Bahl, K., Pilegaard, K., DelSontro, T., Stoy, P., Zona, D., Preface, Towards a full greenhouse gas balance of the biosphere (2015) Biogeosciences, 12, pp. 453-456. , https://doi.org/10.5194/bg-12-453-2015; Nickerson, N., (2016) Evaluating Gas Emission Measurements Using Minimum Detectable Flux (MDF), , Eosense Inc., Dartmouth, Nova Scotia, Canada; Nicolini, G., Castaldi, S., Fratini, G., Valentini, R., A literature overview of micrometeorological CH4 and N2O flux measurements in terrestrial ecosystems (2013) Atmos. Environ, 81, pp. 311-319; O'Connell, C.S., Ruan, L., Silver, W.L., Drought drives rapid shifts in tropical rainforest soil biogeochemistry and greenhouse gas emissions (2018) Nat. Commun, 9, p. 1348. , https://doi.org/10.1038/s41467-018-03352; Oertel, C., Matschullat, J., Zurba, K., Zimmermann, F., Erasmi, S., Greenhouse gas emissions from soils-A review (2016) Chem. Erde-Geochem, 76, pp. 327-352; Petitjean, C., Hénault, C., Perrin, A.-S., Pontet, C., Metay, A., Bernoux, M., Jehanno, T., Roggy, J.-C., Soil N2O emissions in French Guiana after the conversion of tropical forest to agriculture with the chop-And-mulch method (2015) Agr. Ecosyst. Environ, 208, pp. 64-74; Petrakis, S., Seyfferth, A., Kan, J., Inamdar, S., Vargas, R., Influence of experimental extreme water pulses on greenhouse gas emissions from soils (2017) Biogeochemistry, 133, pp. 147-164; Petrakis, S., Barba, J., Bond-Lamberty, B., Vargas, R., Using greenhouse gas fluxes to define soil functional types (2017) Plant Soil, pp. 1-10; Pumpanen, J., Kolari, P., Ilvesniemi, H., Minkkinen, K., Vesala, T., Niinistö, S., Lohila, A., Pihlatie, M., Comparison of different chamber techniques for measuring soil CO2 efflux (2004) Agr. Forest Meteorol, 123, pp. 159-176; Rowland, L., Hill, T.C., Stahl, C., Siebicke, L., Burban, B., Zaragoza-Castells, J., Ponton, S., Williams, M., Evidence for strong seasonality in the carbon storage and carbon use efficiency of an Amazonian forest (2014) Glob. Change Biol, 20, pp. 979-991; Rubio, V.E., Detto, M., Spatiotemporal variability of soil respiration in a seasonal tropical forest (2017) Ecol. Evol, 7, pp. 7104-7116; Savage, K., Phillips, R., Davidson, E., High temporal frequency measurements of greenhouse gas emissions from soils (2014) Biogeosciences, 11, pp. 2709-2720. , https://doi.org/10.5194/bg-11-2709-2014; Silver, W.L., Lugo, A., Keller, M., Soil oxygen availability and biogeochemistry along rainfall and topographic gradients in upland wet tropical forest soils (1999) Biogeochemistry, 44, pp. 301-328; Teh, Y.A., Diem, T., Jones, S., Huaraca Quispe, L.P., Baggs, E., Morley, N., Richards, M., Meir, P., Methane and nitrous oxide fluxes across an elevation gradient in the tropical Peruvian Andes (2014) Biogeosciences, 11, pp. 2325-2339. , https://doi.org/10.5194/bg-11-2325-2014; Verchot, L.V., Davidson, E.A., Cattânio, H., Ackerman, I.L., Erickson, H.E., Keller, M., Land use change and biogeochemical controls of nitrogen oxide emissions from soils in eastern Amazonia (1999) Global Biogeochem. Cy, 13, pp. 31-46; Verchot, L.V., Davidson, E.A., Cattânio, J.H., Ackerman, I.L., Land-use change and biogeochemical controls of methane fluxes in soils of eastern Amazonia (2000) Ecosystems, 3, pp. 41-56; Wagner, F., Hérault, B., Stahl, C., Bonal, D., Rossi, V., Modeling water availability for trees in tropical forests (2011) Agr. Forest Meteorol, 151, pp. 1202-1213 |
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EcoFoG @ webmaster @ |
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860 |
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Verryckt, L.T.; Van Langenhove, L.; Ciais, P.; Courtois, E.A.; Vicca, S.; Peñuelas, J.; Stahl, C.; Coste, S.; Ellsworth, D.S.; Posada, J.M.; Obersteiner, M.; Chave, J.; Janssens, I.A. |
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Coping with branch excision when measuring leaf net photosynthetic rates in a lowland tropical forest |
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Journal Article |
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2020 |
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Biotropica |
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Biotropica |
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52 |
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4 |
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608-615 |
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branch cutting; canopy physiology; French Guiana; gas exchange; photosynthesis; rainforest; stomatal conductance; ecological modeling; environmental conditions; forest canopy; leaf; measurement method; photosynthesis; tree; tropical forest; Gruidae |
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Measuring leaf gas exchange from canopy leaves is fundamental for our understanding of photosynthesis and for a realistic representation of carbon uptake in vegetation models. Since canopy leaves are often difficult to reach, especially in tropical forests with emergent trees up to 60 m at remote places, canopy access techniques such as canopy cranes or towers have facilitated photosynthetic measurements. These structures are expensive and therefore not very common. As an alternative, branches are often cut to enable leaf gas exchange measurements. The effect of branch excision on leaf gas exchange rates should be minimized and quantified to evaluate possible bias. We compared light-saturated leaf net photosynthetic rates measured on excised and intact branches. We selected branches positioned at three canopy positions, estimated relative to the top of the canopy: upper sunlit foliage, middle canopy foliage, and lower canopy foliage. We studied the variation of the effects of branch excision and transport among branches at these different heights in the canopy. After excision and transport, light-saturated leaf net photosynthetic rates were close to zero for most leaves due to stomatal closure. However, when the branch had acclimated to its new environmental conditions—which took on average 20 min—light-saturated leaf net photosynthetic rates did not significantly differ between the excised and intact branches. We therefore conclude that branch excision does not affect the measurement of light-saturated leaf net photosynthesis, provided that the branch is recut under water and is allowed sufficient time to acclimate to its new environmental conditions. © 2020 The Association for Tropical Biology and Conservation |
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UMR 5174 Laboratoire Evolution et Diversité Biologique, Université Paul Sabatier, CNRS, Toulouse, France |
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Blackwell Publishing Ltd |
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00063606 (Issn) |
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EcoFoG @ webmaster @ |
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960 |
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Chevolot, M.; Louisanna, E.; Azri, W.; Leblanc-Fournier, N.; Roeckel-Drevet, P.; Scotti-Saintagne, C.; Scotti, I. |
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Isolation of primers for candidate genes for mechano-sensing in five Neotropical tree species |
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2011 |
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Tree Genetics & Genomes |
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Tree Genet. Genomes |
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7 |
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3 |
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655-661 |
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Population genomics; Functional gene; Mechanical signals; Fabaceae |
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Mechanical signals have an impact on plant development. Tropical rainforest trees display large variability for life-history traits related to biomechanics and therefore are a unique study system to better understand biomechanical trait variability from an evolutionary perspective. From sequences and gene expression data available in model species, we developed specific primers for six candidate genes for mechano-sensing in five tropical species. Most of the gene sequences were polymorphic in most species. |
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[Chevolot, Malia; Louisanna, Eliane; Scotti-Saintagne, Caroline; Scotti, Ivan] INRA, Unite Mixte Rech Ecol Forets Guyane, Kourou 97310, French Guiana, Email: ivan.scotti@ecofog.gf |
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Springer Heidelberg |
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1614-2942 |
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ISI:000290571900018 |
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EcoFoG @ webmaster @ |
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315 |
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Denis, T.; Richard-Hansen, C.; Brunaux, O.; Guitet, S.; Hérault, B. |
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Birds of a feather flock together: Functionally similar vertebrates positively co-occur in Guianan forests |
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2019 |
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Ecosphere |
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Ecosphere |
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10 |
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3 |
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e02566 |
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activity matching; birds; Guiana Shield; information exchange; mammals; mixed-species associations; mutualism; terra firme rainforests |
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Medium- and large-sized vertebrates play a key role in shaping overall forest functioning. Despite this, vertebrate interactions, from competition to mutualism, remain poorly studied, even though these interactions should be taken into account in our conservation and management strategies. Thus, we tackled the question of vertebrate co-occurrence in tropical rainforests: Are (negative or positive) co-occurrences dependent on forest structure and composition? and Are these co-occurrences linked to functional species similarity? We recorded the occurrence of 21 medium- and large-sized vertebrates in 19 French Guianan locations in which a large set of forest structure and composition descriptors were collected. We used a probabilistic model to look for co-occurrences at different spatial scales, and species pairwise co-occurrences were then compared to those generated solely on the basis of forest structure and composition. We then quantified the co-occurrence strength between pairwise species dyads and determined whether they relied on species functional similarity, controlling for the environmental effects. We found that positive co-occurrences vastly outnumbered negative co-occurrences, were only partly shaped by the local environment, and were closely linked to species functional similarity. Thus, groups of species sharing similar functional traits are more prone to co-occur, highlighting the key role of functional redundancy in structuring species assemblages. We discuss how positive interactions could generate the predominance of positive co-occurrences in oligotrophic terra firme (unflooded) forests when resources are scarce and dispersed in dry season. Finally, we identified functional groups based on co-occurrence strength and suggested that frugivory/granivory and body size are of primary importance in species interactions in Neotropical vertebrate communities. © 2019 The Authors. |
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INPHB, Institut National Polytechnique Félix Houphouët-Boigny, Yamoussoukro, Cote d'Ivoire |
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Wiley-Blackwell |
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21508925 (Issn) |
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Export Date: 16 March 2020; Correspondence Address: Denis, T.; Office National de la Chasse et de la Faune Sauvage, UMR EcoFoG (AgroParisTech, Cirad, CNRS, INRA, Université des Antilles, Université de Guyane)France; email: thomas.denis@ecofog.gf |
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EcoFoG @ webmaster @ |
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924 |
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Mony, R.; Dejean, A.; Bilong, C.F.B.; Kenne, M.; Rouland-Lefèvre, C. |
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Melissotarsus ants are likely able to digest plant polysaccharides |
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2013 |
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Comptes Rendus – Biologies |
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C. R. Biol. |
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336 |
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10 |
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500-504 |
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Ant-plant interactions; Degradation of plant material; Enzymatic activity; Melissotarsus ants |
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Melissotarsus ants have an extremely specialized set of behaviours. Both workers and gynes tunnel galleries in their host tree bark. Workers walk with their mesothoracic legs pointing upwards and tend Diaspididae hemiptera for their flesh. The ants use their forelegs to plug the galleries with silk that they secrete themselves. We hypothesised that the ants' energetic needs for nearly constant gallery digging could be satisfied through the absorption of host tree tissues; so, using basic techniques, we examined the digestive capacities of workers from two species. We show that workers are able to degrade oligosaccharides and heterosides as well as, to a lesser degree, polysaccharides. This is one of the rare reports on ants able to digest plant polysaccharides other than starch. © 2013 Académie des sciences. |
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IRD, UMR BIOEMCO-IBIOS, 32, rue Henri-Varagnat, 93143 Bondy cedex, France |
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16310691 (Issn) |
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Export Date: 6 December 2013; Source: Scopus; Coden: Crboc; doi: 10.1016/j.crvi.2013.08.003; Language of Original Document: English; Correspondence Address: Dejean, A.; Université de Toulouse, UPS, Ecolab, 118, route de Narbonne, 31062 Toulouse, France; email: alain.dejean@wanadoo.fr; References: Hölldobler, B., Wilson, E.O., (1990) The Ants, , Harvard University Press Cambridge, MA, USA 730 p; Duchesne, L.C., Larson, D.W., Cellulose and the evolution of plant life (1989) BioScience, 39, pp. 238-241; Watanabe, H., Tokuda, G., Cellulolytic Systems in Insects (2010) Annu. Rev. Entomol., 55, pp. 609-632; Wenzel, M., Schonig, I., Berchtold, M., Kampfer, P., König, K., Aerobic and facultatively anaerobic cellulolytic bacteria from the gut of the Termite Zootermopsis angusticollis (2002) J. Appl. Microbiol., 92, pp. 32-40; Brune, A., Microbial symbioses in the digestive tract of lower termites (2011) Beneficial Microorganisms in Multicellular Life Forms, pp. 3-25. , E. Rosenberg, U. Gophna, Heidelberg Springer; Tokuda, G., Watanabe, H., Hidden cellulases in termites: Revision of an old hypothesis (2007) Biol. Lett., 3, pp. 336-339; Nobre, T., Aanen, D.K., Fungiculture or termite husbandry? The ruminant hypothesis (2012) Insects, 3, pp. 307-323; Zientz, E., Feldhaar, H., Stoll, S., Gross, R., Insights into the microbial world associated with ants (2005) Arch. Microbiol., 184, pp. 199-206; Aylward, F., Burnum, K.E., Scott, J.J., Suen, G., Tringe, S.G., Metagenomic and metaproteomic insights into bacterial communities in leaf-cutter ant fungus gardens (2012) ISME J., pp. 1-14; Cook, S.C., Davidson, D.W., Nutritional and functional biology of exudate-feeding ants (2006) Entomol. Exp. Appl., 118, pp. 1-10; He, H., Chen, Y., Zhang, Y., Wei, C., Bacteria associated with gut lumen of Camponotus japonicus Mayr (2011) Environ. Entomol., 40, pp. 1405-1409; Blochmann, F., Über das Vorkommen von bakterienähnlichen Gebilden in den Geweben und Eiern verschiedener Insekten (1892) Zentbl. Bakteriol., 11, pp. 234-240; Feldhaar, H., Straka, J., Krischke, M., Berthold, K., Stoll, S., Nutritional upgrading for omnivorous carpenter ants by the endosymbiont Blochmannia (2007) BMC Biol., 5, p. 48; De Souza, D.J., Bézier, A., Depoix, D., Drezen, J.M., Lenoir, A., Blochmannia endosymbionts improve colony growth and immune defence in the ant Camponotus fellah (2009) BMC Microbiol., 9, p. 29; Van Borm, S., Buschinger, A., Boomsma, J.J., Billen, J., Tetraponera ants have gut symbionts related to nitrogen-fixing root-nodule bacteria (2002) Proc. R. Soc. Lond. B., 269, pp. 2023-2027; Eilmus, S., Heil, M., Bacterial associates of arboreal ants and their putative functions in an obligate ant-plant mutualism (2009) Appl. Env. Microbiol., 75, pp. 4324-4332; Russell, J.A., Moreau, C.S., Goldman-Huertas, B., Fujiwara, M., Lohman, D.J., Pierce, N.E., Bacterial gut symbionts are tightly linked with the evolution of herbivory in ants (2009) Proc. Natl. Acad. Sci. USA, 106, pp. 21236-21241; Delage-Darchen, B., Une fourmi de Côte d'Ivoire: Melissotarsus titubans Del., N. Sp. (1972) Insect. Soc., 19, pp. 213-226; Prins, A.J., Ben-Dov, Y., Rust, D.J., A new observation on the association between ants (Hymenoptera: Formicidae) and armoured scale insects (Homoptera: Diaspididae) (1975) J. Entomol. Soc. S. Afr., 38, pp. 211-216; Mony, R., Kenne, M., Dejean, A., (2002) Biology and Ecology of Pest Ants of the Genus Melissotarsus (Formicidae: Myrmicinae), with Special Reference to Tropical Fruit Tree Attacks, Sociobiology, 40, pp. 645-654; Mony, R., Fisher, B.L., Kenne, M., Tindo, M., Dejean, A., Behavioural ecology of bark-digging ants of the genus Melissotarsus (2007) Funct. Ecosyst. Commun., 1, pp. 121-128; Fisher, B.L., Robertson, H.G., Silk production by adult workers of the ant Melissotarsus emeryi (Hymenoptera, Formicidae) in South African fynbos (1999) Insect. Soc., 46, pp. 78-83; Sanson, G., The biomechanics of browsing and grazing (2006) Am. J. Bot., 93, pp. 1531-1545; Clissold, F., Sanson, G.D., Read, J., The paradoxical effects nutrient ratios and supply rates on an outbreaking insect herbivore, the Australian plague locust (2006) J. Anim. Ecol., 75, pp. 1000-1013; Cannon, C.A., (1998) Nutritional Ecology of the Carpenter Ant Camponotus Pennsylvanicus (De Geer): Macronutrient Preference and Particle Consumption, , (PhD thesis) Blacsburg VA; Eisner, T., A comparative morphological study of the proventriculus of ants (Hymenoptera, Formicidae) (1957) Bull. Mus. Comp. Zool., 116, pp. 441-490; Caetano, F.H., Can we use the digestive tract for phyllogenetic studies in ants (1990) Social Insects and the Environment, pp. 321-322. , G.K. Veeresh, B. Mallik, C.A. 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Physiol., 99 A, pp. 657-663; Williams, J., Villaroya, H., Petek Galactosidase, F., II, III and IV from seeds of Trifolium repens (1978) Biochem. J., 175, pp. 1069-1077; Werner, W., Rey, H.G., Wielinger, R.H., Properties of a new chromogen for determination of glucose in blood according to the COD/POD method (1970) Anal. Chem., 252, pp. 224-228; Mora, P., Rouland, C., Comparison of hydrolytic enzyme produced during growth on carboidrate substrated by Termitomyces associates of Pseudacanthotermes spiniger and Microtermes subhyalinus (isopteran: Termitidae) (1994) Sociobiology, 26, pp. 39-53; Koning, R.E., Secondary Growth. Plant Physiology Information, , http://plantphys.info/plant_biology/secondary.shtml; Scheffrahn, R.H., Termites (Isoptera) (2008) Encyclopedia of Entomology Part 20, pp. 3737-3747. , J.L. Capinera, Springer Berlin; Richard, F.J., Mora, P., Errard, C., Rouland, C., Digestive capacities of leaf-cutting ants and the contribution of their cultivar to the degradation of plant material (2005) J. Comp. Physiol. B, 175, pp. 297-303; Ayre, G.L., The relationships between food and digestive enzymes in five species of ants (Hymenoptera: Formicidae) (1967) Can. Entomol., 99, pp. 408-411; Went, F.W., Wheeler, J., Wheeler, G.C., Feeding and digestion in some ants (Veromessor and Manica) (1972) BioScience, 22, pp. 82-88; Moller, I.E., De Fine Licht, H.H., Harholt, J., Willats, G.T., Boomsma, J.J., The dynamics of plant cell-wall polysaccharide decomposition in leaf-cutting ant fungus garden (2011) PloS ONE, 6, p. 17506 |
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EcoFoG @ webmaster @ |
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516 |
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