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Leitão, R.P.; Zuanon, J.; Villéger, S.; Williams, S.E.; Baraloto, C.; Fortunel, C.; Mendonça, F.P.; Mouillot, D. |
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Rare species contribute disproportionately to the functional structure of species assemblages |
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Journal Article |
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2016 |
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Proceedings of the Royal Society B: Biological Sciences |
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Proceedings of the Royal Society B: Biological Sciences |
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283 |
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1828 |
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Conservation; Extinction; Functional diversity; Null models; Rarity index; Tropical biodiversity |
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There is broad consensus that the diversity of functional traits within species assemblages drives several ecological processes. It is also widely recognized that rare species are the first to become extinct following human-induced disturbances. Surprisingly, however, the functional importance of rare species is still poorly understood, particularly in tropical species-rich assemblages where the majority of species are rare, and the rate of species extinction can be high. Here, we investigated the consequences of local and regional extinctions on the functional structure of species assemblages. We used three extensive datasets (stream fish from the Brazilian Amazon, rainforest trees from French Guiana, and birds from the Australian Wet Tropics) and built an integrative measure of species rarity versuscommonness, combining local abundance, geographical range, andhabitat breadth. Using different scenarios of species loss, we found a disproportionate impact of rare species extinction for the three groups, with significant reductions in levels of functional richness, specialization, and originality of assemblages, which may severely undermine the integrity of ecological processes. The whole breadth of functional abilities within species assemblages, which is disproportionately supported by rare species, is certainly critical in maintaining ecosystems particularly under the ongoing rapid environmental transitions. © 2016 The Author(s) Published by the Royal Society. All rights reserved. |
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Instituto Federal de Educação, Ciência e Tecnologia, Presidente Figueiredo, Brazil |
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Export Date: 7 May 2016 |
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EcoFoG @ webmaster @ |
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676 |
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Mouillot, D.; Bellwood, D.R.; Baraloto, C.; Chave, J.; Galzin, R.; Harmelin-Vivien, M.; Kulbicki, M.; Lavergne, S.; Lavorel, S.; Mouquet, N.; Paine, C.E.T.; Renaud, J.; Thuiller, W. |
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Rare Species Support Vulnerable Functions in High-Diversity Ecosystems |
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Journal Article |
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2013 |
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PLoS Biology |
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PloS Biol. |
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11 |
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5 |
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e1001569 |
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Around the world, the human-induced collapses of populations and species have triggered a sixth mass extinction crisis, with rare species often being the first to disappear. Although the role of species diversity in the maintenance of ecosystem processes has been widely investigated, the role of rare species remains controversial. A critical issue is whether common species insure against the loss of functions supported by rare species. This issue is even more critical in species-rich ecosystems where high functional redundancy among species is likely and where it is thus often assumed that ecosystem functioning is buffered against species loss. Here, using extensive datasets of species occurrences and functional traits from three highly diverse ecosystems (846 coral reef fishes, 2,979 alpine plants, and 662 tropical trees), we demonstrate that the most distinct combinations of traits are supported predominantly by rare species both in terms of local abundance and regional occupancy. Moreover, species that have low functional redundancy and are likely to support the most vulnerable functions, with no other species carrying similar combinations of traits, are rarer than expected by chance in all three ecosystems. For instance, 63% and 98% of fish species that are likely to support highly vulnerable functions in coral reef ecosystems are locally and regionally rare, respectively. For alpine plants, 32% and 89% of such species are locally and regionally rare, respectively. Remarkably, 47% of fish species and 55% of tropical tree species that are likely to support highly vulnerable functions have only one individual per sample on average. Our results emphasize the importance of rare species conservation, even in highly diverse ecosystems, which are thought to exhibit high functional redundancy. Rare species offer more than aesthetic, cultural, or taxonomic diversity value; they disproportionately increase the potential breadth of functions provided by ecosystems across spatial scales. As such, they are likely to insure against future uncertainty arising from climate change and the ever-increasing anthropogenic pressures on ecosystems. Our results call for a more detailed understanding of the role of rarity and functional vulnerability in ecosystem functioning. © 2013 Mouillot et al. |
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Biological and Environmental Sciences, University of Stirling, Stirling, United Kingdom |
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Export Date: 12 June 2013; Source: Scopus; Art. No.: e1001569; Coden: Pblib; :doi 10.1371/journal.pbio.1001569; Language of Original Document: English; Correspondence Address: Mouillot, D.; Unité Mixte de Recherche (UMR) Centre National de la Recherche Scientifique (CNRS)-UM2, Institut français de recherche pour l'exploitation de la mer (IFREMER), Institute for Research and Development (IRD) 5119 ECOSYM, Université Montpellier 2 cc 093, Montpellier, France; email: david.mouillot@univ-montp2.fr |
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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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Title |
Rarity of monodominance in hyperdiverse Amazonian forests |
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Journal Article |
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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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EcoFoG @ webmaster @ |
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887 |
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Dejean, A.; Corbara, B. |
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Reactions by army ant workers to nestmates having had contact with sympatric ant species |
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Journal Article |
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2014 |
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Comptes Rendus Biologies |
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C. R. Biol. |
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337 |
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11 |
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642-645 |
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Army ants Antipredation Colony-mate recognition Eciton Transferring cuticular compounds; Eciton; Formicidae |
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It was recently shown that Pheidole megacephala colonies (an invasive species originating from Africa) counterattack when raided by the army ant, Eciton burchellii. The subsequent contact permits Pheidole cuticular compounds (that constitute the “colony odour”) to be transferred onto the raiding Eciton, which are then not recognised by their colony-mates and killed. Using a simple method for transferring cuticular compounds, we tested if this phenomenon occurs for Neotropical ants. Eciton workers rubbed with ants from four sympatric species were released among their colony-mates. Individuals rubbed with Solenopsis saevissima or Camponotus blandus workers were attacked, but not those rubbed with Atta sexdens, Pheidole fallax or with colony-mates (control lot). So, the chemicals of certain sympatric ant species, but not others, trigger intra-colonial aggressiveness in Eciton. We conclude that prey-ant chemicals might have played a role in the evolution of army ant predatory behaviour, likely influencing prey specialization in certain cases. |
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Clermont Université, Université Blaise-Pascal, LMGE, BP 10448Clermont-Ferrand, France |
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Elsevier Masson SAS |
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Export Date: 12 November 2014; Coden: Crboc; Correspondence Address: Dejean, A.; CNRS, É Cologie des Forêts de Guyane, UMR-CNRS 8172, BP 316, France |
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Nirma, C.; Eparvier, V.; Stien, D. |
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Reactivation of antibiosis in the entomogenous fungus Chrysoporthe sp. SNB-CN74 |
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2015 |
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Journal of Antibiotics |
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Journal of Antibiotics |
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68 |
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9 |
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586-590 |
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Chrysoporthe sp. SNB-CN74 was isolated from a Nasutitermes corniger nest, and its ethyl acetate extract was found to exhibit very strong antibacterial activity. Two antibacterial metabolites were isolated, (-)-R-skyrin (2) and (+)-rugulosin A (3). Eventually, the fungus lost its antibiotic potential when subcultured, and the use of yeast extract induced the re-expression of these two antibiotics. Yeast extract possibly activated a cryptic pathway by mimicking the presence of an ecological competitor. © 2015 Japan Antibiotics Research Association All rights reserved. |
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Sorbonne Universités, Laboratoire de Biodiversité et Biotechnologies Microbiennes (LBBM), Observatoire Océanologique, Banyuls-sur-mer, France |
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Export Date: 12 October 2015 |
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EcoFoG @ webmaster @ |
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628 |
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Le Guen, R.; Corbara, B.; Rossi, V.; Azémar, F.; Dejean, A. |
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Reciprocal protection from natural enemies in an ant-wasp association |
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2015 |
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Comptes Rendus – Biologies |
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Comptes Rendus – Biologies |
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338 |
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4 |
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255-259 |
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Aggressiveness; Arboreal ants; Azteca; Polybia; Protection mutualism; Social wasps |
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Abstract We show that in French Guiana the large carton nests of Azteca chartifex, a territorially-dominant arboreal dolichoderine ant, are protected from bird attacks when this ant lives in association with Polybia rejecta, an epiponine social wasp. Because A. chartifex colonies are well known for their ability to divert army ant raids from the base of their host tree so that they protect their associated wasps from these raids, there is a reciprocal benefit for these two partners, permitting us to call this association a mutualism. We also show that P. rejecta nests are significantly less often attacked by birds than are those of two compared epiponine social wasp species. Furthermore, experimentation using a standardized protocol demonstrated the significantly higher aggressiveness of P. rejecta compared to seven other wasp species. We conclude that the efficacious protection of its associated ant nests is likely due to the extreme aggressiveness of P. rejecta. © 2015 Académie des sciences. Published by Elsevier Masson SAS. All rights reserved. |
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CNRS, Écologie des forêts de Guyane (UMR-CNRS 8172), Campus agronomique, BP 316Kourou cedex, France |
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Export Date: 24 April 2015 |
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600 |
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Herault, B. |
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Reconciling niche and neutrality through the Emergent Group approach |
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2007 |
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Perspectives in Plant Ecology Evolution and Systematics |
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Perspect. Plant Ecol. Evol. Syst. |
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9 |
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71-78 |
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Biodiversity; ecological equivalency; biological traits; neutral theory; niche differentiation; redundancy |
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Both niche and neutral theories have been suggested as potential frameworks for modelling biodiversity. Niche models assume that biological traits represent evolutionary adaptations and define individuals in terms of functional trade-offs. Neutral models assume that all individuals at a single trophic level are functionally equivalent on a per capita basis with respect to their birth, death, dispersal and speciation. The opinion of many researchers is that neutral and niche processes operate simultaneously to generate diversity without knowing how the unification of both models can be achieved. Recently, several theoretical papers have reported evidence on the evolutionary emergence of niche structures shaping the emergence of groups of similar species. In this way, an Emergent Group is defined as a set of species that have a similar functional niche owing to a convergent ecological strategy. Central to the Emergent Group concept are the assumptions of functional equivalence within and of functional divergence between Emergent Groups. Within an Emergent Group, species richness is subject to a zero-sum rule set by the balance between the rate of individual loss and of immigration. Between Emergent Groups, tradeoffs such as seed size/seedling competitivity, investment in reproductive system/investment in vegetative systems or competitive ability/predator invulnerability are cornerstones of the evolutionary divergence. Delineating Emergent Groups amounts to reaching a compromise between maximizing niche differentiation (i.e. maximizing differences in functional tradeoffs) between Emergent Groups and maximizing neutrality within Emergent Groups. Up to now, the Emergent Group concept has been mostly proposed by theoretical scientists but it should be tested by empirical ecologists. The way in which niche and neutral models could be combined provides a profitable opportunity for theoretical and empirical scientists to collaborate fruitfully. (c) 2007 Rubel Foundation, ETH Zurich. Published by Elsevier GmbH. All rights reserved. |
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[Herault, Bruno] Univ Antilles Guyane, UMR Ecol Forets Guyane, F-97379 Kourou, France, Email: Bruno.Herault@cirad.fr |
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ELSEVIER GMBH, URBAN & FISCHER VERLAG |
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1433-8319 |
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ISI:000251685100002 |
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Sist, P.; Sheil, D.; Kartawinata, K.; Priyadi, H. |
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Reduced-impact logging in Indonesian Borneo: some results confirming the need for new silvicultural prescriptions |
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2003 |
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Forest Ecology and Management |
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For. Ecol. Manage. |
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179 |
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1-3 |
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415-427 |
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Reduced-impact logging (RIL) and conventional techniques (CNV) were compared in a mixed dipterocarp hill forest in East Kalimantan in three blocks of about 100 ha each. Damage was evaluated using pre- and post-harvesting assessments in 24 one-hectare sample plots. RIL techniques nearly halved the number of trees destroyed (36 vs 60 trees/ha). RIL's main benefit was in the reduction of skidding damage (9.5% of the original tree population in RIL vs 25% in CNV). Before logging, mean canopy openness in CNV (three plots only) and RIL (9 plots) was similar (3.6 and 3.1%) and not significantly different (x(2) = 2.73, P = 0.254). After logging, the mean canopy openness was 19.2% in CNV (n = 9 plots) and 13.3% in RIL (n = 8 plots), and the distributions of the canopy class in RIL and CNV significantly different x(2) = 43.56, P < 0.001). CNV plots showed a higher proportion of measurements in the most open class greater than or equal to30% than in RIL. At a larger scale, the area of skidtrail per unit timber volume extracted was halved in the RIL compartment (15 m(2) vs 27 m(2) m(-3) for CNV). However, under high felling intensity (>8 trees/ha), both stand damage and canopy disturbance in RIL approached those recorded in CNV under low or moderate felling regime. Over this felling intensity threshold the effectiveness of RIL in reducing tree damage is limited. In mixed dipterocarp forest where harvestable timber density generally exceeds 10 trees/ha, a minimum diameter felling limit is clearly insufficient to keep extraction rates below 8 trees/ha. Based on these new results and previous studies in Borneo, we suggest three silvicultural rules: (1) to keep a minimum distance between stumps of ca. 40 m, (2) to ensure only single tree gaps using directional felling, (3) to harvest only stems with 60-100 cm dbh. Foresters, policy makers and certifiers should consider these as criteria for sustainable forest management. We emphasise the need to expand harvesting studies to look at impacts and trade-offs across larger forest landscapes, to expand RIL beyond silvicultural concepts and to include the maintenance of other forest goods and services. (C) 2002 Elsevier Science B.V. All rights reserved. |
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WOS:000183836300033 |
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EcoFoG @ webmaster @ |
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311 |
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Herault, B.; Bornet, A.; Tremolieres, M. |
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Title |
Redundancy and niche differentiation among the European invasive Elodea species |
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2008 |
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Biological Invasions |
Abbreviated Journal |
Biol. Invasions |
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10 |
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7 |
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1099-1107 |
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biological traits; functional equivalence; invasivness; niche overlapping; waterweeds |
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Community ecologists implicitly assume redundancy when they aggregate species into functional groups. But there have been remarkably few empirical efforts to investigate the accuracy of this concept in situ. The concept of redundancy could be roughly split into two components: the ecological redundancy (similar response to environmental variations involving similar ecological processes) and the functional redundancy (similar biological trait combinations shaping similar functional processes). Both types of redundancy are tested among the 3 invasive European Elodeas. In 11 sites and during two successive years 2004-2005, the cover growth rate of each Elodea species was monthly recorded. To test ecological redundancy, cover growth rates were related to a large suite of environmental variables. To test functional redundancy, 13 biological traits involved in competitive relationships were measured each month. Firstly, the redundancy hypothesis looks problematic for Elodea ernstiae. Indeed, the later possess numerous biological traits involved in light competition and niche overlap with the other Elodeas is very low. Secondly, ecological and functional redundancy can be successfully applied to Elodea canadensis and Elodea nuttallii. They share a large suite of biological traits leading to wide niche overlaps through the growing season. And the measured environmental variables do not differentially influence their growth rates, which are, in turn, controlled by a similar group of biological traits. In this way, the different invasiveness patterns of E. canadensis and E. nuttallii could be solely due to the ecological drift and their ecological dynamic could follow neutral rules. |
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[Herault, Bruno] Univ Antilles Guyane, INRA, UMR Ecol Forets Guyane, F-97379 Kourou, France, Email: Bruno.Herault@cirad.fr |
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SPRINGER |
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1387-3547 |
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ISI:000258704400015 |
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EcoFoG @ eric.marcon @ |
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131 |
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Chave, J.; Navarrete, D.; Almeida, S.; Alvarez, E.; Aragao, L.E.O.C.; Bonal, D.; Chatelet, P.; Silva-Espejo, J.E.; Goret, J.Y.; von Hildebrand, P.; Jimenez, E.; Patino, S.; Penuela, M.C.; Phillips, O.L.; Stevenson, P.; Malhi, Y. |
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Title |
Regional and seasonal patterns of litterfall in tropical South America |
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Journal Article |
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2010 |
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Biogeosciences |
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Biogeosciences |
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7 |
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1 |
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43-55 |
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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 results. |
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[Chave, J.] CNRS UPS, Lab Evolut & Divers Biol, UMR 5174, Toulouse, France, Email: chave@cict.fr |
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COPERNICUS GESELLSCHAFT MBH |
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1726-4170 |
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ISI:000274058100004 |
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EcoFoG @ eric.marcon @ |
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70 |
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