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Maurice, L.; López, F.; Becerra, S.; Jamhoury, H.; Le Menach, K.; Dévier, M.-H.; Budzinski, H.; Prunier, J.; Juteau-Martineau, G.; Ochoa-Herrera, V.; Quiroga, D.; Schreck, E. |
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Drinking water quality in areas impacted by oil activities in Ecuador: Associated health risks and social perception of human exposure |
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2019 |
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Science of the Total Environment |
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Sci. Total Environ. |
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690 |
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1203-1217 |
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Demineralized waters; Domestic waters; Hydrocarbons; Metal(loid)s; Oil activities; Social risk perception; Benzene refining; Health; Health risks; Hydrocarbons; Petroleum refineries; Petroleum refining; Polycyclic aromatic hydrocarbons; Potable water; Risk assessment; Risk perception; Toluene; Trace elements; Water quality; Water wells; Zinc; Arsenic concentration; Demineralized water; Domestic water; Information sources; Living conditions; Microbiological analysis; Natural backgrounds; Oil activities; Water distribution systems |
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The unregulated oil exploitation in the Northern Ecuadorian Amazon Region (NEAR), mainly from 1964 to the 90's, led to toxic compounds largely released into the environment. A large majority of people living in the Amazon region have no access to drinking water distribution systems and collects water from rain, wells or small streams. The concentrations of major ions, trace elements, PAHs (polycyclic aromatic hydrocarbons) and BTEX (benzene, toluene, ethylbenzene, xylenes) were analyzed in different water sources to evaluate the impacts of oil extraction and refining. Samples were taken from the NEAR and around the main refinery of the country (Esmeraldas Oil Refinery/State Oil Company of Ecuador) and were compared with domestic waters from the Southern region, not affected by petroleum activities. In most of the samples, microbiological analysis revealed a high level of coliforms representing significant health risks. All measured chemical compounds in waters were in line with national and international guidelines, except for manganese, zinc and aluminum. In several deep-water wells, close to oil camps, toluene concentrations were higher than the natural background while PAHs concentrations never exceeded individually 2 ng·L−1. Water ingestion represented 99% of the total exposure pathways for carcinogenic and non-carcinogenic elements (mainly zinc) in adults and children, while 20% to 49% of the Total Cancer Risk was caused by arsenic concentrations. The health index (HI) indicates acceptable chronic effects for domestic use according the US-EPA thresholds. Nevertheless, these limits do not consider the cocktail effects of metallic and organic compounds. Furthermore, they do not include the social determinants of human exposure, such as socio-economic living conditions or vulnerability. Most (72%) of interviewed families knew sanitary risks but a discrepancy was observed between knowledge and action: religious beliefs, cultural patterns, information sources, experience and emotions play an important role front to exposure. © 2019 |
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Department of Environmental Sciences and Engineering, Gillings School of Global Public Health, University of North Carolina at Chapel HillNC 2759, United States |
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Elsevier B.V. |
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00489697 (Issn) |
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EcoFoG @ webmaster @ |
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877 |
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Pavoine, S.; Marcon, E.; Ricotta, C. |
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‘Equivalent numbers’ for species, phylogenetic or functional diversity in a nested hierarchy of multiple scales |
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Journal Article |
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2016 |
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Methods in Ecology and Evolution |
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Methods in Ecology and Evolution |
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7 |
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10 |
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1152-1163 |
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alpha diversity; beta diversity; biodiversity; community ecology; community phylogenetics; diversity apportionment; gamma diversity; quadratic entropy |
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Many recent studies have searched to integrate species’ functions and phylogenies in the measurement of biodiversity. To obtain easily interpretable measures, some researchers recommended diversity indices expressed in terms of equivalent numbers of species: the number of equally likely and maximally dissimilar species needed to produce the given value of diversity. Then, biodiversity is often calculated at three scales: within communities (α diversity), among communities (β diversity) and in a region (γ diversity). These three scales are, however, insufficient to tackle the organization of biodiversity in space because, for most organisms, there is a nested hierarchy of multiple scales characterized by different patterns and processes, from the small neighbourhood to the biosphere. We developed methodologies for analysing species, functional, taxonomic or phylogenetic diversity in a hierarchy of multiple scales using equivalent numbers of species. As an example, we analysed the taxonomic and functional diversity of macroinvertebrate assemblages in the Loire River, France, at four levels: within sites (α diversity), among sites within geological regions (β1 diversity), among geological regions (β2 diversity) and at the river scale (γ diversity). The new hierarchical approaches of biodiversity revealed very low differences among sites within regions and among regions in terms of taxonomy and functional traits (size and diet), despite moderate, significant species turnover among geological regions. We compare our framework with those other authors have developed. We argue that different definitions of α, β, γ diversities are used in the literature reflecting different points of view on biodiversity. We make recommendations on how to normalize functional (or phylogenetic) dissimilarities among species to render sites and regions comparable, and discuss the pros and cons of our approach. The hierarchical approaches of biodiversity in terms of ‘equivalent numbers’ respond to current demands to obtain intuitive, easily interpretable components of biodiversity. The approaches we propose go beyond current developments by considering a hierarchy of spatial scales and unbalanced sampling design. They will provide powerful tools to detect the ecological and evolutionary processes that act differently at different scales. © 2016 The Authors. Methods in Ecology and Evolution © 2016 British Ecological Society |
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Department of Environmental Biology, University of Rome ‘La Sapienza’, Piazzale Aldo Moro 5, Rome, Italy |
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Export Date: 20 October 2016 |
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EcoFoG @ webmaster @ |
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697 |
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Fortunel, C.; Paine, C.E.T.; Fine, P.V.A.; Mesones, I.; Goret, J.; Burban, B.; Cazal, J.; Baraloto, C.; Comita, L. |
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There's no place like home: seedling mortality contributes to the habitat specialisation of tree species across Amazonia |
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Journal Article |
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2016 |
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Ecology Letters |
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Ecology Letters |
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19 |
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10 |
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1256-1266 |
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Amazon basin; forests habitats; habitat association; herbivory; light availability; plant lineages; rainfall temporal variation; seedling performance; soil fertility; tropical trees |
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Understanding the mechanisms generating species distributions remains a challenge, especially in hyperdiverse tropical forests. We evaluated the role of rainfall variation, soil gradients and herbivory on seedling mortality, and how variation in seedling performance along these gradients contributes to habitat specialisation. In a 4-year experiment, replicated at the two extremes of the Amazon basin, we reciprocally transplanted 4638 tree seedlings of 41 habitat-specialist species from seven phylogenetic lineages among the three most important forest habitats of lowland Amazonia. Rainfall variation, flooding and soil gradients strongly influenced seedling mortality, whereas herbivory had negligible impact. Seedling mortality varied strongly among habitats, consistent with predictions for habitat specialists in most lineages. This suggests that seedling performance is a primary determinant of the habitat associations of adult trees across Amazonia. It further suggests that tree diversity, currently mostly harboured in terra firme forests, may be strongly impacted by the predicted climate changes in Amazonia. © 2016 John Wiley & Sons Ltd/CNRS |
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Department of Ecology and Evolutionary Biology, University of California, Los Angeles, CA, United States |
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Export Date: 27 October 2016 |
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698 |
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Falster, D.S.; Duursma, R.A.; Ishihara, M.I.; Barneche, D.R.; FitzJohn, R.G.; Vårhammar, A.; Aiba, M.; Ando, M.; Anten, N.; Aspinwall, M.J.; Baltzer, J.L.; Baraloto, C.; Battaglia, M.; Battles, J.J.; Lamberty, B.B.; Van Breugel, M.; Camac, J.; Claveau, Y.; Coll, L.; Dannoura, M.; Delagrange, S.; Domec, J.C.; Fatemi, F.; Feng, W.; Gargaglione, V.; Goto, Y.; Hagihara, A.; Hall, J.S.; Hamilton, S.; Harja, D.; Hiura, T.; Holdaway, R.; Hutley, L.B.; Ichie, T.; Jokela, E.J.; Kantola, A.; Kelly, J.W.G.; Kenzo, T.; King, D.; Kloeppel, B.D.; Kohyama, T.; Komiyama, A.; Laclau, J.P.; Lusk, C.H.; Maguire, D.A.; Le Maire, G.; Mäkelä, A.; Markesteijn, L.; Marshall, J.; McCulloh, K.; Miyata, I.; Mokany, K.; Mori, S.; Myster, R.W.; Nagano, M.; Naidu, S.L.; Nouvellon, Y.; O'Grady, A.P.; O'Hara, K.L.; Ohtsuka, T.; Osada, N.; Osunkoya, O.O.; Peri, P.L.; Petritan, A.M.; Poorter, L.; Portsmuth, A.; Potvin, C.; Ransijn, J.; Reid, D.; Ribeiro, S.C.; Roberts, S.D.; Rodríguez, R.; Acosta, A.S.; Santa-Regina, I.; Sasa, K.; Selaya, N.G.; Sillett, S.C.; Sterck, F.; Takagi, K.; Tange, T.; Tanouchi, H.; Tissue, D.; Umehara, T.; Utsugi, H.; Vadeboncoeur, M.A.; Valladares, F.; Vanninen, P.; Wang, J.R.; Wenk, E.; Williams, R.; De Aquino Ximenes, F.; Yamaba, A.; Yamada, T.; Yamakura, T.; Yanai, R.D.; York, R.A. |
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Title |
BAAD: a Biomass And Allometry Database for woody plants |
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Journal Article |
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2015 |
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Ecology |
Abbreviated Journal |
Ecology |
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96 |
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5 |
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1445 |
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Allometric equations; Biomass allocation; Biomass partitioning; Global carbon cycle; Plant allometry; Plant traits |
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Understanding how plants are constructed; i.e., how key size dimensions and the amount of mass invested in different tissues varies among individuals; is essential for modeling plant growth, estimating carbon stocks, and mapping energy fluxes in the terrestrial biosphere. Allocation patterns can differ through ontogeny, but also among coexisting species and among species adapted to different environments. While a variety of models dealing with biomass allocation exist, we lack a synthetic understanding of the underlying processes. This is partly due to the lack of suitable data sets for validating and parameterizing models. To that end, we present the Biomass and allometry database (BAAD) for woody plants. The BAAD contains 259 634 measurements collected in 176 different studies, from 21 084 individuals across 678 species. Most of these data come from existing publications. However, raw data were rarely made public at time of publication. Thus the BAAD contains individual level data from different studies, transformed into standard units and variable names. The transformations were achieved using a common workflow for all raw data files. Other features that distinguish the BAAD are: (i) measurements were for individual plants rather than stand averages; (ii) individuals spanning a range of sizes were measured; (iii) inclusion of plants from 0.01-100 m in height; and (iii) biomass was estimated directly, i.e., not indirectly via allometric equations (except in very large trees where biomass was estimated from detailed subsampling). We included both wild and artificially grown plants. The data set contains the following size metrics: total leaf area; area of stem crosssection including sapwood, heartwood, and bark; height of plant and crown base, crown area, and surface area; and the dry mass of leaf, stem, branches, sapwood, heartwood, bark, coarse roots, and fine root tissues. We also report other properties of individuals (age, leaf size, leaf mass per area, wood density, nitrogen content of leaves and wood), as well as information about the growing environment (location, light, experimental treatment, vegetation type) where available. It is our hope that making these data available will improve our ability to understand plant growth, ecosystem dynamics, and carbon cycling in the world's vegetation. |
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Department of Disturbance Ecology, University of Bayreuth, Germany |
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Export Date: 1 September 2016 |
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EcoFoG @ webmaster @ |
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686 |
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Verheyen, K.; Vanhellemont, M.; Auge, H.; Baeten, L.; Baraloto, C.; Barsoum, N.; Bilodeau-Gauthier, S.; Bruelheide, H.; Castagneyrol, B.; Godbold, D.; Haase, J.; Hector, A.; Jactel, H.; Koricheva, J.; Loreau, M.; Mereu, S.; Messier, C.; Muys, B.; Nolet, P.; Paquette, A.; Parker, J.; Perring, M.; Ponette, Q.; Potvin, C.; Reich, P.; Smith, A.; Weih, M.; Scherer-Lorenzen, M. |
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Contributions of a global network of tree diversity experiments to sustainable forest plantations |
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2016 |
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Ambio |
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Ambio |
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45 |
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1 |
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29-41 |
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Biodiversity experiments; Ecological restoration; Functional biodiversity research; Plantation forest; Sustainable forest management |
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The area of forest plantations is increasing worldwide helping to meet timber demand and protect natural forests. However, with global change, monospecific plantations are increasingly vulnerable to abiotic and biotic disturbances. As an adaption measure we need to move to plantations that are more diverse in genotypes, species, and structure, with a design underpinned by science. TreeDivNet, a global network of tree diversity experiments, responds to this need by assessing the advantages and disadvantages of mixed species plantations. The network currently consists of 18 experiments, distributed over 36 sites and five ecoregions. With plantations 1–15 years old, TreeDivNet can already provide relevant data for forest policy and management. In this paper, we highlight some early results on the carbon sequestration and pest resistance potential of more diverse plantations. Finally, suggestions are made for new, innovative experiments in understudied regions to complement the existing network. © 2015, Royal Swedish Academy of Sciences. |
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Department of Crop Production Ecology, Swedish University of Agricultural Sciences, PO Box 7043, Uppsala, Sweden |
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Export Date: 29 January 2016 |
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652 |
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Vanbellingen, Q.P.; Fu, T.; Bich, C.; Amusant, N.; Stien, D.; Della-Negra, S.; Touboul, D.; Brunelle, A. |
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Mapping Dicorynia guianensis Amsh. wood constituents by submicron resolution cluster-TOF-SIMS imaging |
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2016 |
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Journal of Mass Spectrometry |
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Journal of Mass Spectrometry |
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51 |
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6 |
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412-423 |
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Dicorynia guianensis; heartwood formation; mass spectrometry imaging; Tof-Sims; tropical wood; tryptamine |
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The preparation of tropical wood surface sections for time-of-flight secondary ion mass spectrometry imaging is described, and the use of delayed extraction of secondary ions and its interest for the analysis of vegetal surface are shown. The method has been applied to the study by time-of-flight secondary ion mass spectrometry imaging with a resolution of less than one micron of a tropical wood species, Dicorynia guianensis, which is one of the most exploited wood in French Guiana for its durable heartwood. The heartwood of this species exhibits an economical importance, but its production is not controlled in forestry. Results show an increase of tryptamine from the transition zone and a concomitant decrease of inorganic ions and starch fragment ions. These experiments lead to a better understanding of the heartwood formation and the origin of the natural durability of D. guianensis. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd. |
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Department of Chemistry and Biochemistry, Florida International University, Miami, FL, United States |
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Export Date: 28 June 2016 |
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EcoFoG @ webmaster @ |
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684 |
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Chartier, M.; Gibernau, M.; Renner, S.S. |
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The evolution of pollinator-plant interaction types in the araceae |
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2014 |
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Evolution |
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Evolution |
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68 |
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5 |
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1533-1543 |
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Ancestral state reconstruction; Inflorescence traits; Phylogeny; Pollination syndromes; Trap flowers |
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Most plant-pollinator interactions are mutualistic, involving rewards provided by flowers or inflorescences to pollinators. Antagonistic plant-pollinator interactions, in which flowers offer no rewards, are rare and concentrated in a few families including Araceae. In the latter, they involve trapping of pollinators, which are released loaded with pollen but unrewarded. To understand the evolution of such systems, we compiled data on the pollinators and types of interactions, and coded 21 characters, including interaction type, pollinator order, and 19 floral traits. A phylogenetic framework comes from a matrix of plastid and new nuclear DNA sequences for 135 species from 119 genera (5342 nucleotides). The ancestral pollination interaction in Araceae was reconstructed as probably rewarding albeit with low confidence because information is available for only 56 of the 120-130 genera. Bayesian stochastic trait mapping showed that spadix zonation, presence of an appendix, and flower sexuality were correlated with pollination interaction type. In the Araceae, having unisexual flowers appears to have provided the morphological precondition for the evolution of traps. Compared with the frequency of shifts between deceptive and rewarding pollination systems in orchids, our results indicate less lability in the Araceae, probably because of morphologically and sexually more specialized inflorescences. © 2013 The Society for the Study of Evolution. |
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Department of Biology, University of Munich, Munich, 80638, Germany |
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Society for the Study of Evolution |
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15585646 (Issn) |
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Export Date: 30 May 2014; Source: Scopus; Coden: Evola; Language of Original Document: English |
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Ter Steege, H.; Henkel, T.W.; Helal, N.; Marimon, B.S.; Marimon-Junior, B.H.; Huth, A.; Groeneveld, J.; Sabatier, D.; Coelho, L.S.; Filho, D.A.L.; Salomão, R.P.; Amaral, I.L.; Matos, F.D.A.; Castilho, C.V.; Phillips, O.L.; Guevara, J.E.; Carim, M.J.V.; Cárdenas López, D.; Magnusson, W.E.; Wittmann, F.; Irume, M.V.; Martins, M.P.; Guimarães, J.R.D.S.; Molino, J.-F.; Bánki, O.S.; Piedade, M.T.F.; Pitman, N.C.A.; Mendoza, A.M.; Ramos, J.F.; Luize, B.G.; Moraes de Leão Novo, E.M.; Núñez Vargas, P.; Silva, T.S.F.; Venticinque, E.M.; Manzatto, A.G.; Reis, N.F.C.; Terborgh, J.; Casula, K.R.; Honorio Coronado, E.N.; Montero, J.C.; Feldpausch, T.R.; Duque, A.; Costa, F.R.C.; Arboleda, N.C.; Schöngart, J.; Killeen, T.J.; Vasquez, R.; Mostacedo, B.; Demarchi, L.O.; Assis, R.L.; Baraloto, C.; Engel, J.; Petronelli, P.; Castellanos, H.; de Medeiros, M.B.; Quaresma, A.; Simon, M.F.; Andrade, A.; Camargo, J.L.; Laurance, S.G.W.; Laurance, W.F.; Rincón, L.M.; Schietti, J.; Sousa, T.R.; de Sousa Farias, E.; Lopes, M.A.; Magalhães, J.L.L.; Mendonça Nascimento, H.E.; Lima de Queiroz, H.; Aymard C, G.A.; Brienen, R.; Revilla, J.D.C.; Vieira, I.C.G.; Cintra, B.B.L.; Stevenson, P.R.; Feitosa, Y.O.; Duivenvoorden, J.F.; Mogollón, H.F.; Araujo-Murakami, A.; Ferreira, L.V.; Lozada, J.R.; Comiskey, J.A.; de Toledo, J.J.; Damasco, G.; Dávila, N.; Draper, F.; García-Villacorta, R.; Lopes, A.; Vicentini, A.; Alonso, A.; Dallmeier, F.; Gomes, V.H.F.; Lloyd, J.; Neill, D.; de Aguiar, D.P.P.; Arroyo, L.; Carvalho, F.A.; de Souza, F.C.; do Amaral, D.D.; Feeley, K.J.; Gribel, R.; Pansonato, M.P.; Barlow, J.; Berenguer, E.; Ferreira, J.; Fine, P.V.A.; Guedes, M.C.; Jimenez, E.M.; Licona, J.C.; Peñuela Mora, M.C.; Villa, B.; Cerón, C.; Maas, P.; Silveira, M.; Stropp, J.; Thomas, R.; Baker, T.R.; Daly, D.; Dexter, K.G.; Huamantupa-Chuquimaco, I.; Milliken, W.; Pennington, T.; Ríos Paredes, M.; Fuentes, A.; Klitgaard, B.; Pena, J.L.M.; Peres, C.A.; Silman, M.R.; Tello, J.S.; Chave, J.; Cornejo Valverde, F.; Di Fiore, A.; Hilário, R.R.; Phillips, J.F.; Rivas-Torres, G.; van Andel, T.R.; von Hildebrand, P.; Noronha, J.C.; Barbosa, E.M.; Barbosa, F.R.; de Matos Bonates, L.C.; Carpanedo, R.S.; Dávila Doza, H.P.; Fonty, É.; GómeZárate Z, R.; Gonzales, T.; Gallardo Gonzales, G.P.; Hoffman, B.; Junqueira, A.B.; Malhi, Y.; Miranda, I.P.A.; Pinto, L.F.M.; Prieto, A.; Rodrigues, D.J.; Rudas, A.; Ruschel, A.R.; Silva, N.; Vela, C.I.A.; Vos, V.A.; Zent, E.L.; Zent, S.; Weiss Albuquerque, B.; Cano, A.; Carrero Márquez, Y.A.; Correa, D.F.; Costa, J.B.P.; Flores, B.M.; Galbraith, D.; Holmgren, M.; Kalamandeen, M.; Nascimento, M.T.; Oliveira, A.A.; Ramirez-Angulo, H.; Rocha, M.; Scudeller, V.V.; Sierra, R.; Tirado, M.; Umaña Medina, M.N.; van der Heijden, G.; Vilanova Torre, E.; Vriesendorp, C.; Wang, O.; Young, K.R.; Ahuite Reategui, M.A.; Baider, C.; Balslev, H.; Cárdenas, S.; Casas, L.F.; Farfan-Rios, W.; Ferreira, C.; Linares-Palomino, R.; Mendoza, C.; Mesones, I.; Torres-Lezama, A.; Giraldo, L.E.U.; Villarroel, D.; Zagt, R.; Alexiades, M.N.; de Oliveira, E.A.; Garcia-Cabrera, K.; Hernandez, L.; Palacios Cuenca, W.; Pansini, S.; Pauletto, D.; Ramirez Arevalo, F.; Sampaio, A.F.; Sandoval, E.H.V.; Valenzuela Gamarra, L.; Levesley, A.; Pickavance, G.; Melgaço, K. |
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Rarity of monodominance in hyperdiverse Amazonian forests |
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2019 |
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Scientific reports |
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Scientific reports |
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9 |
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1 |
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13822 |
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Tropical forests are known for their high diversity. Yet, forest patches do occur in the tropics where a single tree species is dominant. Such “monodominant” forests are known from all of the main tropical regions. For Amazonia, we sampled the occurrence of monodominance in a massive, basin-wide database of forest-inventory plots from the Amazon Tree Diversity Network (ATDN). Utilizing a simple defining metric of at least half of the trees over 10cm diameter belonging to one species, we found only a few occurrences of monodominance in Amazonia, and the phenomenon was not significantly linked to previously hypothesized life history traits such wood density, seed mass, ectomycorrhizal associations, or Rhizobium nodulation. In our analysis, coppicing (the formation of sprouts at the base of the tree or on roots) was the only trait significantly linked to monodominance. While at specific locales coppicing or ectomycorrhizal associations may confer a considerable advantage to a tree species and lead to its monodominance, very few species have these traits. Mining of the ATDN dataset suggests that monodominance is quite rare in Amazonia, and may be linked primarily to edaphic factors. |
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Department of Biology, University of Missouri, St. Louis, MO, 63121, USA |
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Export Date: 7 October 2019 |
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Vedel, V.; Cerdan, A.; Martinez, Q.; Baraloto, C.; Petitclerc, F.; Orivel, J.; Fortunel, C. |
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Day-time vs. Night-time sampling does not affect estimates of spider diversity across a land use gradient in the Neotropics |
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2015 |
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Journal of Arachnology |
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Journal of Arachnology |
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43 |
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3 |
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413-416 |
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Araneae; community; day; night; sampling protocol |
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To obtain a reliable description of spider communities, robust sampling protocols are crucial. However, it remains unclear if descriptions of spider communities in tropical habitats require both day and night sampling. Here we tested whether sampling both day and night in high and low vegetation strata would lead to better diversity estimates of spider communities than sampling at only one period of the day. We determined spider taxonomic diversity in a network of 12 plots in French Guiana along a vegetation gradient. We found high alpha diversity of spiders as expected for a tropical area at every site. We showed strong differences in spider alpha and beta diversity between high and low vegetation strata, while they were similar between day and night sampling. Our results suggest that collecting spiders at only one period is sufficient to describe the diversity of spider communities across land use types in the neotropics. © The American Arachnological Society. |
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Department of Biology, University of Maryland, College Park, MD, United States |
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Export Date: 10 December 2015 |
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Fortunel, C.; Fine, P.V.A.; Baraloto, C. |
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Leaf, stem and root tissue strategies across 758 Neotropical tree species |
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2012 |
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Functional Ecology |
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Funct. Ecol. |
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26 |
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5 |
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1153-1161 |
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French Guiana; Functional trade-offs; Leaf economics; Peru; Plant traits; Tropical forest; Wood economics |
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1. Trade-offs among functional traits reveal major plant strategies that can give insight into species distributions and ecosystem processes. However, current identification of plant strategies lacks the integration of root structural traits together with leaf and stem traits. 2. We examined correlations among 14 traits representing leaf, stem and woody root tissues. Traits were measured on 1084 individuals representing 758 Neotropical tree species, across 13 sites representative of the environmental variation encompassed by three widespread habitats (seasonally flooded, clay terra firme and white-sand forests) at opposite ends of Amazonia (French Guiana and Peru). 3. Woody root traits were closely aligned with stem traits, but not with leaf traits. Altogether leaf, stem and woody root traits delineated two orthogonal axes of functional trade-offs: a first axis defined by leaf traits, corresponding to a 'leaf economics spectrum', and a second axis defined by covarying stem and woody root traits, corresponding to a 'wood economics spectrum'. These axes remained consistent when accounting for species evolutionary history with phylogenetically independent contrasts. 4. Despite the strong species turnover across sites, the covariation among root and stem structural traits as well as their orthogonality to leaf traits were strongly consistent across habitats and regions. 5. We conclude that root structural traits mirrored stem traits rather than leaf traits in Neotropical trees. Leaf and wood traits define an integrated whole-plant strategy in lowland South American forests that may contribute to a more complete understanding of plant responses to global changes in both correlative and modelling approaches. We suggest further meta-analyses in expanded environmental and geographic zones to determine the generality of this pattern. © 2012 The Authors. Functional Ecology © 2012 British Ecological Society. |
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Department of Biology, University of Florida, Gainesville, FL, 32611, United States |
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Export Date: 10 October 2012; Source: Scopus; Coden: Fecoe; doi: 10.1111/j.1365-2435.2012.02020.x; Language of Original Document: English; Correspondence Address: Fortunel, C.; INRA, UMR Ecologie des Forêts de Guyane, BP 709, 97387 Kourou Cedex, France; email: claire.fortunel@ecofog.gf |
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