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Dejean, A.; Corbara, B.; Azémar, F.; Carpenter, J.M. |
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When attempts at robbing prey turn fatal |
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Journal Article |
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2012 |
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Naturwissenschaften |
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Naturwissenschaften |
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99 |
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7 |
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579-582 |
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Ant predation; Azteca andreae; Cleptobiosis; Flies and dung beetles; Myrmecophyte; Reduviidae; Socialwasps; Stinglessbees |
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Because group-hunting arboreal ants spread-eagle insect prey for a long time before retrieving them, these prey can be coveted by predatory flying insects. Yet, attempting to rob these prey is risky if the ant species is also an effective predator. Here, we show that trying to rob prey from Azteca andreae workers is a fatal error as 268 out of 276 potential cleptobionts (97.1 %) were captured in turn. The ant workers hunt in a group and use the “Velcro®” principle to cling firmly to the leaves of their host tree, permitting them to capture very large prey. Exceptions were one social wasp, plus some Trigona spp. workers and flies that landed directly on the prey and were able to take off immediately when attacked. We conclude that in this situation, previously captured prey attract potential cleptobionts that are captured in turn in most of the cases. © Springer-Verlag 2012. |
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Division of Invertebrate Zoology, American Museum of Natural History, Central Park West at 79th Street, New York, NY 10024, United States |
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00281042 (Issn) |
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Export Date: 30 July 2012; Source: Scopus; Coden: Natwa; doi: 10.1007/s00114-012-0929-x; Language of Original Document: English; Correspondence Address: Dejean, A.; CNRS, Écologie des Forêts de Guyane (UMR-CNRS 8172), Campus agronomique, BP 316, 97379 Kourou cedex, France; email: alain.dejean@wanadoo.fr |
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EcoFoG @ webmaster @ |
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417 |
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Dejean, A.; Revel, M.; Azémar, F.; Roux, O. |
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Altruism during predation in an assassin bug |
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Journal Article |
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2013 |
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Naturwissenschaften |
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Naturwissenschaften |
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100 |
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10 |
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913-922 |
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Conspecific tolerance; Predation; Prey sharing; Reduviidae; Zelus annulosus |
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Zelus annulosus is an assassin bug species mostly noted on Hirtella physophora, a myrmecophyte specifically associated with the ant Allomerus decemarticulatus known to build traps on host tree twigs to ambush insect preys. The Z. annulosus females lay egg clutches protected by a sticky substance. To avoid being trapped, the first three instars of nymphs remain grouped in a clutch beneath the leaves on which they hatched, yet from time to time, they climb onto the upper side to group ambush preys. Long-distance prey detection permits these bugs to capture flying or jumping insects that alight on their leaves. Like some other Zelus species, the sticky substance of the sundew setae on their forelegs aids in prey capture. Group ambushing permits early instars to capture insects that they then share or not depending on prey size and the hunger of the successful nymphs. Fourth and fifth instars, with greater needs, rather ambush solitarily on different host tree leaves, but attract siblings to share large preys. Communal feeding permits faster prey consumption, enabling small nymphs to return sooner to the shelter of their leaves. By improving the regularity of feeding for each nymph, it likely regulates nymphal development, synchronizing molting and subsequently limiting cannibalism. © 2013 Springer-Verlag Berlin Heidelberg. |
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IRD, Maladies Infectieuses et Vecteurs, Ecologie, Genetique, Evolution et Controle (UMR-IRD 224), IRD 01, BP 171, Bobo-Dioulasso, Burkina Faso |
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00281042 (Issn) |
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Export Date: 30 October 2013; Source: Scopus; Coden: Natwa; doi: 10.1007/s00114-013-1091-9; Language of Original Document: English; Correspondence Address: Dejean, A.; Écologie des Forêts de Guyane, Campus Agronomique, BP 316, 97379 Kourou cedex, France; email: alain.dejean@wanadoo.fr |
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EcoFoG @ webmaster @ |
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508 |
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Dejean, A.; Labrière, N.; Touchard, A.; Petitclerc, F.; Roux, O. |
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Nesting habits shape feeding preferences and predatory behavior in an ant genus |
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Journal Article |
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2014 |
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Naturwissenschaften |
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Naturwissenschaften |
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101 |
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4 |
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323-330 |
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Ant genus Pseudomyrmex; Arboreal and ground nesting; Feeding preferences; Myrmecophytism; Predation |
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We tested if nesting habits influence ant feeding preferences and predatory behavior in the monophyletic genus Pseudomyrmex (Pseudomyrmecinae) which comprises terrestrial and arboreal species, and, among the latter, plant-ants which are obligate inhabitants of myrmecophytes (i.e., plants sheltering so-called plant-ants in hollow structures). A cafeteria experiment revealed that the diet of ground-nesting Pseudomyrmex consists mostly of prey and that of arboreal species consists mostly of sugary substances, whereas the plant-ants discarded all the food we provided. Workers forage solitarily, detecting prey from a distance thanks to their hypertrophied eyes. Approach is followed by antennal contact, seizure, and the manipulation of the prey to sting it under its thorax (next to the ventral nerve cord). Arboreal species were not more efficient at capturing prey than were ground-nesting species. A large worker size favors prey capture. Workers from ground- and arboreal-nesting species show several uncommon behavioral traits, each known in different ant genera from different subfamilies: leaping abilities, the use of surface tension strengths to transport liquids, short-range recruitment followed by conflicts between nestmates, the consumption of the prey's hemolymph, and the retrieval of entire prey or pieces of prey after having cut it up. Yet, we never noted group ambushing. We also confirmed that Pseudomyrmex plant-ants live in a kind of food autarky as they feed only on rewards produced by their host myrmecophyte, or on honeydew produced by the hemipterans they attend and possibly on the fungi they cultivate. © 2014 Springer-Verlag Berlin Heidelberg. |
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IRD, MIVEGEC (IRD 224-CNRS 5290-UM1-UM2), Équipe BEES, 911 avenue Agropolis, 34394 Montpellier Cedex 5, France |
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Springer Verlag |
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Export Date: 5 May 2014; Source: Scopus; Coden: Natwa; Language of Original Document: English; Correspondence Address: Dejean, A.; CNRS, Écologie des Forêts de Guyane (UMR-CNRS 8172), Campus Agronomique, BP 316, 97379 Kourou cedex, France; email: alain.dejean@wanadoo.fr |
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EcoFoG @ webmaster @ |
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539 |
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Leguet, A.; Gibernau, M.; Shintu, L.; Caldarelli, S.; Moja, S.; Baudino, S.; Caissard, J.-C. |
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Evidence for early intracellular accumulation of volatile compounds during spadix development in Arum italicum L. and preliminary data on some tropical Aroids |
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Journal Article |
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2014 |
Publication |
Naturwissenschaften |
Abbreviated Journal |
Naturwissenschaften |
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101 |
Issue |
8 |
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623-635 |
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Araceae; Cytochemistry; Gas chromatography; Nuclear magnetic resonance; Volatile compounds |
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Staining and histochemistry of volatile organic compounds (VOCs) were performed at different inflorescence developmental stages on nine aroid species; one temperate, Arum italicum and eight tropical from the genera Caladium, Dieffenbachia and Philodendron. Moreover, a qualitative and quantitative analysis of VOCs constituting the scent of A. italicum, depending on the stage of development of inflorescences was also conducted. In all nine species, vesicles were observed in the conical cells of either the appendix or the stamens (thecae) and the staminodes. VOCs were localised in intracellular vesicles from the early stages of inflorescence development until their release during receptivity of gynoecium. This localisation was observed by the increase of both number and diameter of the vesicles during 1 week before receptivity. Afterwards, vesicles were fewer and smaller but rarely absent. In A. italicum, staining and gas chromatography analyses confirmed that the vesicles contained terpenes. The quantitatively most important ones were the sesquiterpenes, but monoterpenes were not negligible. Indeed, the quantities of terpenes matched the vesicles' size evolution during 1 week. Furthermore, VOCs from different biosynthetic pathways (sesquiterpenes and alkanes) were at their maximum quantity 2 days before gynoecium receptivity (sesquiterpenes and alkanes) or during receptivity (isobutylamine, monoterpenes, skatole and p-cresol). VOCs seemed to be emitted during gynoecium receptivity and/or during thermogenesis, and FADs are accumulated after thermogenesis in the spadix. These complex dynamics of the different VOCs could indicate specialisation of some VOCs and cell machinery to attract pollinators on the one hand and to repulse/protect against phytophagous organisms and pathogens after pollination on the other hand. © 2014 Springer-Verlag Berlin Heidelberg. |
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CNRS, UMR-6134 SPE, 20000 Ajaccio, France |
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Springer Verlag |
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Export Date: 1 September 2014; Coden: Natwa; Correspondence Address: Gibernau, M.; CNRS, UMR-6134 SPE, 20000 Ajaccio, France; email: gibernau@univ-corse.fr |
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558 |
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Fauset, S.; Johnson, M.O.; Gloor, M.; Baker, T.R.; Monteagudo M., A.; Brienen, R.J.W.; Feldpausch, T.R.; Lopez-Gonzalez, G.; Malhi, Y.; Ter Steege, H.; Pitman, N.C.A.; Baraloto, C.; Engel, J.; Petronelli, P.; Andrade, A.; Camargo, J.L.C.; Laurance, S.G.W.; Laurance, W.F.; Chave, J.; Allie, E.; Vargas, P.N.; Terborgh, J.W.; Ruokolainen, K.; Silveira, M.; Aymard C., G.A.; Arroyo, L.; Bonal, D.; Ramirez-Angulo, H.; Araujo-Murakami, A.; Neill, D.; Herault, B.; Dourdain, A.; Torres-Lezama, A.; Marimon, B.S.; Salomão, R.P.; Comiskey, J.A.; Réjou-Méchain, M.; Toledo, M.; Licona, J.C.; Alarcón, A.; Prieto, A.; Rudas, A.; Van Der Meer, P.J.; Killeen, T.J.; Marimon Junior, B.-H.; Poorter, L.; Boot, R.G.A.; Stergios, B.; Torre, E.V.; Costa, F.R.C.; Levis, C.; Schietti, J.; Souza, P.; Groot, N.; Arets, E.; Moscoso, V.C.; Castro, W.; Coronado, E.N.H.; Peña-Claros, M.; Stahl, C.; Barroso, J.; Talbot, J.; Vieira, I.C.G.; Van Der Heijden, G.; Thomas, R.; Vos, V.A.; Almeida, E.C.; Davila, E.Á.; Aragão, L.E.O.C.; Erwin, T.L.; Morandi, P.S.; De Oliveira, E.A.; Valadão, M.B.X.; Zagt, R.J.; Van Der Hout, P.; Loayza, P.A.; Pipoly, J.J.; Wang, O.; Alexiades, M.; Cerón, C.E.; Huamantupa-Chuquimaco, I.; Di Fiore, A.; Peacock, J.; Camacho, N.C.P.; Umetsu, R.K.; De Camargo, P.B.; Burnham, R.J.; Herrera, R.; Quesada, C.A.; Stropp, J.; Vieira, S.A.; Steininger, M.; Rodríguez, C.R.; Restrepo, Z.; Muelbert, A.E.; Lewis, S.L.; Pickavance, G.C.; Phillips, O.L. |
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Title |
Hyperdominance in Amazonian forest carbon cycling |
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Journal Article |
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2015 |
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Nature Communications |
Abbreviated Journal |
Nature Communications |
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6 |
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6857 |
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While Amazonian forests are extraordinarily diverse, the abundance of trees is skewed strongly towards relatively few â € hyperdominantâ €™ species. In addition to their diversity, Amazonian trees are a key component of the global carbon cycle, assimilating and storing more carbon than any other ecosystem on Earth. Here we ask, using a unique data set of 530 forest plots, if the functions of storing and producing woody carbon are concentrated in a small number of tree species, whether the most abundant species also dominate carbon cycling, and whether dominant species are characterized by specific functional traits. We find that dominance of forest function is even more concentrated in a few species than is dominance of tree abundance, with only â ‰1% of Amazon tree species responsible for 50% of carbon storage and productivity. Although those species that contribute most to biomass and productivity are often abundant, species maximum size is also influential, while the identity and ranking of dominant species varies by function and by region. © 2015 Macmillan Publishers Limited. All rights reserved. |
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Instituto de Biologia, Universidade Estadual de CampinasCampinas, Brazil |
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Export Date: 18 May 2015 |
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Steidinger, B.S.; Crowther, T.W.; Liang, J.; Van Nuland, M.E.; Werner, G.D.A.; Reich, P.B.; Nabuurs, G.; de-Miguel, S.; Zhou, M.; Picard, N.; Herault, B.; Zhao, X.; Zhang, C.; Routh, D.; Peay, K.G.; Abegg, M.; Adou Yao, C.Y.; Alberti, G.; Almeyda Zambrano, A.; Alvarez-Davila, E.; Alvarez-Loayza, P.; Alves, L.F.; Ammer, C.; Antón-Fernández, C.; Araujo-Murakami, A.; Arroyo, L.; Avitabile, V.; Aymard, G.; Baker, T.; Bałazy, R.; Banki, O.; Barroso, J.; Bastian, M.; Bastin, J.-F.; Birigazzi, L.; Birnbaum, P.; Bitariho, R.; Boeckx, P.; Bongers, F.; Bouriaud, O.; Brancalion, P.H.S.; Brandl, S.; Brearley, F.Q.; Brienen, R.; Broadbent, E.; Bruelheide, H.; Bussotti, F.; Cazzolla Gatti, R.; Cesar, R.; Cesljar, G.; Chazdon, R.; Chen, H.Y.H.; Chisholm, C.; Cienciala, E.; Clark, C.J.; Clark, D.; Colletta, G.; Condit, R.; Coomes, D.; Cornejo Valverde, F.; Corral-Rivas, J.J.; Crim, P.; Cumming, J.; Dayanandan, S.; de Gasper, A.L.; Decuyper, M.; Derroire, G.; DeVries, B.; Djordjevic, I.; Iêda, A.; Dourdain, A.; Obiang, N.L.E.; Enquist, B.; Eyre, T.; Fandohan, A.B.; Fayle, T.M.; Feldpausch, T.R.; Finér, L.; Fischer, M.; Fletcher, C.; Fridman, J.; Frizzera, L.; Gamarra, J.G.P.; Gianelle, D.; Glick, H.B.; Harris, D.; Hector, A.; Hemp, A.; Hengeveld, G.; Herbohn, J.; Herold, M.; Hillers, A.; Honorio Coronado, E.N.; Huber, M.; Hui, C.; Cho, H.; Ibanez, T.; Jung, I.; Imai, N.; Jagodzinski, A.M.; Jaroszewicz, B.; Johannsen, V.; Joly, C.A.; Jucker, T.; Karminov, V.; Kartawinata, K.; Kearsley, E.; Kenfack, D.; Kennard, D.; Kepfer-Rojas, S.; Keppel, G.; Khan, M.L.; Killeen, T.; Kim, H.S.; Kitayama, K.; Köhl, M.; Korjus, H.; Kraxner, F.; Laarmann, D.; Lang, M.; Lewis, S.; Lu, H.; Lukina, N.; Maitner, B.; Malhi, Y.; Marcon, E.; Marimon, B.S.; Marimon-Junior, B.H.; Marshall, A.R.; Martin, E.; Martynenko, O.; Meave, J.A.; Melo-Cruz, O.; Mendoza, C.; Merow, C.; Monteagudo Mendoza, A.; Moreno, V.; Mukul, S.A.; Mundhenk, P.; Nava-Miranda, M.G.; Neill, D.; Neldner, V.; Nevenic, R.; Ngugi, M.; Niklaus, P.; Oleksyn, J.; Ontikov, P.; Ortiz-Malavasi, E.; Pan, Y.; Paquette, A.; Parada-Gutierrez, A.; Parfenova, E.; Park, M.; Parren, M.; Parthasarathy, N.; Peri, P.L.; Pfautsch, S.; Phillips, O.; Piedade, M.T.; Piotto, D.; Pitman, N.C.A.; Polo, I.; Poorter, L.; Poulsen, A.D.; Poulsen, J.R.; Pretzsch, H.; Ramirez Arevalo, F.; Restrepo-Correa, Z.; Rodeghiero, M.; Rolim, S.; Roopsind, A.; Rovero, F.; Rutishauser, E.; Saikia, P.; Saner, P.; Schall, P.; Schelhaas, M.-J.; Schepaschenko, D.; Scherer-Lorenzen, M.; Schmid, B.; Schöngart, J.; Searle, E.; Seben, V.; Serra-Diaz, J.M.; Salas-Eljatib, C.; Sheil, D.; Shvidenko, A.; Silva-Espejo, J.; Silveira, M.; Singh, J.; Sist, P.; Slik, F.; Sonké, B.; Souza, A.F.; Stereńczak, K.; Svenning, J.-C.; Svoboda, M.; Targhetta, N.; Tchebakova, N.; Steege, H.; Thomas, R.; Tikhonova, E.; Umunay, P.; Usoltsev, V.; Valladares, F.; van der Plas, F.; Van Do, T.; Vasquez Martinez, R.; Verbeeck, H.; Viana, H.; Vieira, S.; von Gadow, K.; Wang, H.-F.; Watson, J.; Westerlund, B.; Wiser, S.; Wittmann, F.; Wortel, V.; Zagt, R.; Zawila-Niedzwiecki, T.; Zhu, Z.-X.; Zo-Bi, I.C.; GFBI consortium |
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Climatic controls of decomposition drive the global biogeography of forest-tree symbioses |
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Journal Article |
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2019 |
Publication |
Nature |
Abbreviated Journal |
Nature |
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569 |
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7756 |
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404-408 |
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Fungi |
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The identity of the dominant root-associated microbial symbionts in a forest determines the ability of trees to access limiting nutrients from atmospheric or soil pools 1,2 , sequester carbon 3,4 and withstand the effects of climate change 5,6 . Characterizing the global distribution of these symbioses and identifying the factors that control this distribution are thus integral to understanding the present and future functioning of forest ecosystems. Here we generate a spatially explicit global map of the symbiotic status of forests, using a database of over 1.1 million forest inventory plots that collectively contain over 28,000 tree species. Our analyses indicate that climate variables—in particular, climatically controlled variation in the rate of decomposition—are the primary drivers of the global distribution of major symbioses. We estimate that ectomycorrhizal trees, which represent only 2% of all plant species 7 , constitute approximately 60% of tree stems on Earth. Ectomycorrhizal symbiosis dominates forests in which seasonally cold and dry climates inhibit decomposition, and is the predominant form of symbiosis at high latitudes and elevation. By contrast, arbuscular mycorrhizal trees dominate in aseasonal, warm tropical forests, and occur with ectomycorrhizal trees in temperate biomes in which seasonally warm-and-wet climates enhance decomposition. Continental transitions between forests dominated by ectomycorrhizal or arbuscular mycorrhizal trees occur relatively abruptly along climate-driven decomposition gradients; these transitions are probably caused by positive feedback effects between plants and microorganisms. Symbiotic nitrogen fixers—which are insensitive to climatic controls on decomposition (compared with mycorrhizal fungi)—are most abundant in arid biomes with alkaline soils and high maximum temperatures. The climatically driven global symbiosis gradient that we document provides a spatially explicit quantitative understanding of microbial symbioses at the global scale, and demonstrates the critical role of microbial mutualisms in shaping the distribution of plant species. © 2019, The Author(s), under exclusive licence to Springer Nature Limited. |
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Faculty of Environmental Sciences and Natural Resource Management, Norwegian University of Life Sciences, Ås, Norway |
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Nature Publishing Group |
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00280836 (Issn) |
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Brienen, R.J.W.; Phillips, O.L.; Feldpausch, T.R.; Gloor, E.; Baker, T.R.; Lloyd, J.; Lopez-Gonzalez, G.; Monteagudo-Mendoza, A.; Malhi, Y.; Lewis, S.L.; Vásquez Martinez, R.; Alexiades, M.; Álvarez Dávila, E.; Alvarez-Loayza, P.; Andrade, A.; Aragaõ, L.E.O.C.; Araujo-Murakami, A.; Arets, E.J.M.M.; Arroyo, L.; Aymard C., G.A.; Bánki, O.S.; Baraloto, C.; Barroso, J.; Bonal, D.; Boot, R.G.A.; Camargo, J.L.C.; Castilho, C.V.; Chama, V.; Chao, K.J.; Chave, J.; Comiskey, J.A.; Cornejo Valverde, F.; Da Costa, L.; De Oliveira, E.A.; Di Fiore, A.; Erwin, T.L.; Fauset, S.; Forsthofer, M.; Galbraith, D.R.; Grahame, E.S.; Groot, N.; Herault, B.; Higuchi, N.; Honorio Coronado, E.N.; Keeling, H.; Killeen, T.J.; Laurance, W.F.; Laurance, S.; Licona, J.; Magnussen, W.E.; Marimon, B.S.; Marimon-Junior, B.H.; Mendoza, C.; Neill, D.A.; Nogueira, E.M.; Núñez, P.; Pallqui Camacho, N.C.; Parada, A.; Pardo-Molina, G.; Peacock, J.; Penã-Claros, M.; Pickavance, G.C.; Pitman, N.C.A.; Poorter, L.; Prieto, A.; Quesada, C.A.; Ramírez, F.; Ramírez-Angulo, H.; Restrepo, Z.; Roopsind, A.; Rudas, A.; Salomaõ, R.P.; Schwarz, M.; Silva, N.; Silva-Espejo, J.E.; Silveira, M.; Stropp, J.; Talbot, J.; Ter Steege, H.; Teran-Aguilar, J.; Terborgh, J.; Thomas-Caesar, R.; Toledo, M.; Torello-Raventos, M.; Umetsu, R.K.; Van Der Heijden, G.M.F.; Van Der Hout, P.; Guimarães Vieira, I.C.; Vieira, S.A.; Vilanova, E.; Vos, V.A.; Zagt, R.J. |
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Long-term decline of the Amazon carbon sink |
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Journal Article |
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2015 |
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Nature |
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Nature |
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519 |
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7543 |
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344-348 |
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Atmospheric carbon dioxide records indicate that the land surface has acted as a strong global carbon sink over recent decades, with a substantial fraction of this sink probably located in the tropics, particularly in the Amazon. Nevertheless, it is unclear how the terrestrial carbon sink will evolve as climate and atmospheric composition continue to change. Here we analyse the historical evolution of the biomass dynamics of the Amazon rainforest over three decades using a distributed network of 321 plots. While this analysis confirms that Amazon forests have acted as a long-term net biomass sink, we find a long-term decreasing trend of carbon accumulation. Rates of net increase in above-ground biomass declined by one-third during the past decade compared to the 1990s. This is a consequence of growth rate increases levelling off recently, while biomass mortality persistently increased throughout, leading to a shortening of carbon residence times. Potential drivers for the mortality increase include greater climate variability, and feedbacks of faster growth on mortality, resulting in shortened tree longevity. The observed decline of the Amazon sink diverges markedly from the recent increase in terrestrial carbon uptake at the global scale, and is contrary to expectations based on models. © 2015 2015 Macmillan Publishers Limited. |
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Centro de Investigación y Promoción Del Campesinado, C/Nicanor Gonzalo Salvatierra Nu 362Riberalta, Bolivia |
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Export Date: 1 April 2015 |
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591 |
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Kunstler, G.; Falster, D.; Coomes, D.A.; Hui, F.; Kooyman, R.M.; Laughlin, D.C.; Poorter, L.; Vanderwel, M.; Vieilledent, G.; Wright, S.J.; Aiba, M.; Baraloto, C.; Caspersen, J.; Cornelissen, J.H.C.; Gourlet-Fleury, S.; Hanewinkel, M.; Herault, B.; Kattge, J.; Kurokawa, H.; Onoda, Y.; Peñuelas, J.; Poorter, H.; Uriarte, M.; Richardson, S.; Ruiz-Benito, P.; Sun, I.-F.; Ståhl, G.; Swenson, N.G.; Thompson, J.; Westerlund, B.; Wirth, C.; Zavala, M.A.; Zeng, H.; Zimmerman, J.K.; Zimmermann, N.E.; Westoby, M. |
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Title |
Plant functional traits have globally consistent effects on competition |
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Journal Article |
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2016 |
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Nature |
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Nature |
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529 |
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7585 |
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204-207 |
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Phenotypic traits and their associated trade-offs have been shown to have globally consistent effects on individual plant physiological functions, but how these effects scale up to influence competition, a key driver of community assembly in terrestrial vegetation, has remained unclear. Here we use growth data from more than 3 million trees in over 140,000 plots across the world to show how three key functional traits – wood density, specific leaf area and maximum height – consistently influence competitive interactions. Fast maximum growth of a species was correlated negatively with its wood density in all biomes, and positively with its specific leaf area in most biomes. Low wood density was also correlated with a low ability to tolerate competition and a low competitive effect on neighbours, while high specific leaf area was correlated with a low competitive effect. Thus, traits generate trade-offs between performance with competition versus performance without competition, a fundamental ingredient in the classical hypothesis that the coexistence of plant species is enabled via differentiation in their successional strategies. Competition within species was stronger than between species, but an increase in trait dissimilarity between species had little influence in weakening competition. No benefit of dissimilarity was detected for specific leaf area or wood density, and only a weak benefit for maximum height. Our trait-based approach to modelling competition makes generalization possible across the forest ecosystems of the world and their highly diverse species composition. © 2016 Macmillan Publishers Limited. All rights reserved. |
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Forestry and Forest Products Research Institute, Tsukuba, Japan |
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Cited By :1; Export Date: 29 January 2016 |
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653 |
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Díaz, S.; Kattge, J.; Cornelissen, J.H.C.; Wright, I.J.; Lavorel, S.; Dray, S.; Reu, B.; Kleyer, M.; Wirth, C.; Colin Prentice, I.; Garnier, E.; Bönisch, G.; Westoby, M.; Poorter, H.; Reich, P.B.; Moles, A.T.; Dickie, J.; Gillison, A.N.; Zanne, A.E.; Chave, J.; Joseph Wright, S.; Sheremet’ev, S.N.; Jactel, H.; Baraloto, C.; Cerabolini, B.; Pierce, S.; Shipley, B.; Kirkup, D.; Casanoves, F.; Joswig, J.S.; Günther, A.; Falczuk, V.; Rüger, N.; Mahecha, M.D.; Gorné, L.D. |
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Title |
The global spectrum of plant form and function |
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Journal Article |
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2016 |
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Nature |
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Nature |
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529 |
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7585 |
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167-171 |
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Earth is home to a remarkable diversity of plant forms and life histories, yet comparatively few essential trait combinations have proved evolutionarily viable in today’s terrestrial biosphere. By analysing worldwide variation in six major traits critical to growth, survival and reproduction within the largest sample of vascular plant species ever compiled, we found that occupancy of six-dimensional trait space is strongly concentrated, indicating coordination and trade-offs. Three-quarters of trait variation is captured in a two-dimensional global spectrum of plant form and function. One major dimension within this plane reflects the size of whole plants and their parts; the other represents the leaf economics spectrum, which balances leaf construction costs against growth potential. The global plant trait spectrum provides a backdrop for elucidating constraints on evolution, for functionally qualifying species and ecosystems, and for improving models that predict future vegetation based on continuous variation in plant form and function. |
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Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. |
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0028-0836 |
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654 |
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Duval, R.; Duplais, C. |
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Fluorescent natural products as probes and tracers in biology |
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2017 |
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Natural Product Reports |
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Natural Product Reports |
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34 |
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2 |
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161-193 |
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Covering: 1985 up to the end of 2016 Fluorescence is a remarkable property of many natural products in addition to their medicinal and biological values. Herein, we provide a review on these peculiar secondary metabolites to stimulate prospecting of them as original fluorescent tracers, endowed with unique photophysical properties and with applications in most fields of biology. The compounds are spectrally categorized (i.e. fluorescing from violet to the near infra-red) and further structurally classified within each category. Natural products selected for their high impact in modern fluorescence-based biological studies are highlighted throughout the article. Finally, we discuss aspects of chemical ecology where fluorescent natural products might have key evolutionary roles and thus open new research directions in the field. © 2017 The Royal Society of Chemistry. |
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CNRS, UMR 8172 EcoFoG (Ecologie des Forêts de Guyane), AgroParisTech, Cirad, INRA, Université des Antilles, Université de Guyane, 23 avenue Pasteur, Cayenne, France |
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