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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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Title |
Climatic controls of decomposition drive the global biogeography of forest-tree symbioses |
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Journal Article |
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2019 |
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Nature |
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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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00280836 (Issn) |
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Aili, S.R.; Touchard, A.; Hayward, R.; Robinson, S.D.; Pineda, S.S.; Lalagüe, H.; Mrinalini; Vetter, I.; Undheim, E.A.B.; Kini, R.M.; Escoubas, P.; Padula, M.P.; Myers, G.S.A.; Nicholson, G.M. |
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Title |
An integrated proteomic and transcriptomic analysis reveals the venom complexity of the bullet ant Paraponera clavata |
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Journal Article |
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2020 |
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Toxins |
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Toxins |
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12 |
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5 |
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DRG neurons; Hyaluronidase; Neurotoxins; Paraponeritoxin; Phospholipases; Rp-Hplc; alpha latrotoxin; ant venom; arginine kinase; cathepsin; contig; defensin 2; hyaluronidase; icarapin; metalloproteinase; neurotoxin; novel toxin like protein; phospholipase; phospholipase A2; poneratoxin; proteome; serine proteinase; transcriptome; unclassified drug; amino acid sequence; ant; Article; liquid chromatography-mass spectrometry; neurotoxicity; nonhuman; Paraponera clavata; protein expression; proteomics; sequence database; tandem mass spectrometry; transcriptomics; venom gland |
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A critical hurdle in ant venom proteomic investigations is the lack of databases to comprehensively and specifically identify the sequence and function of venom proteins and peptides. To resolve this, we used venom gland transcriptomics to generate a sequence database that was used to assign the tandem mass spectrometry (MS) fragmentation spectra of venom peptides and proteins to specific transcripts. This was performed alongside a shotgun liquid chromatography-mass spectrometry (LC-MS/MS) analysis of the venom to confirm that these assigned transcripts were expressed as proteins. Through the combined transcriptomic and proteomic investigation of Paraponera clavata venom, we identified four times the number of proteins previously identified using 2D-PAGE alone. In addition to this, by mining the transcriptomic data, we identified several novel peptide sequences for future pharmacological investigations, some of which conform with inhibitor cysteine knot motifs. These types of peptides have the potential to be developed into pharmaceutical or bioinsecticide peptides. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. |
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Faculty of Science, University of Nice, Nice, 06000, France |
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20726651 (Issn) |
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EcoFoG @ webmaster @ |
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972 |
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Vleminckx, J.; Bauman, D.; Demanet, M.; Hardy, O.J.; Doucet, J.-L.; Drouet, T. |
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Title |
Past human disturbances and soil fertility both influence the distribution of light-demanding tree species in a Central African tropical forest |
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Journal Article |
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2020 |
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Journal of Vegetation Science |
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J. Veg. Sci. |
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31 |
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3 |
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440-453 |
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light-demanding species; moist tropical forests; past human disturbances; shade-bearer species; soil charcoal abundance; soil properties; tree community assemblages; wood-specific gravity; anthropogenic effect; forest canopy; forest ecosystem; shifting cultivation; soil fertility; soil property; tree; tropical forest; Cameroon |
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Questions: In vast areas of Central African forests, the upper canopy is presently dominated by light-demanding tree species. Here, we confront three hypotheses to explain this dominance: (a) these species have expanded their distribution because of widespread past slash-and-burn activities, as suggested by important charcoal amounts recorded in the soils of the region; (b) their abundance is rather explained by soil properties, as this guild establishes preferentially on favourable physico-chemical conditions for rapid growth; (c) soil properties have been substantially influenced by past human disturbances and those two effects cannot be disentangled. Location: Pallisco-CIFM logging concession, southeastern Cameroon (300,000 ha). Methods: We quantified soil charcoal abundance and measured ten soil variables at the basis of 60 target trees that belonged to a list of three long-living pioneer light-demanding (LLP) and four shade-bearer (SB) species. We identified all stems with a diameter at breast height (DBH) ≥ 20 cm within a distance of 15 m around each target tree. Species were characterised by their wood-specific gravity (WSG), which reflected their light requirement. Multiple regression models were used to quantify and test the relative effects of charcoal abundance and soil variables on the mean WSG of the 60 tree communities, as well as the abundance of three guilds: LLP, SB, and non-pioneer light demanders (NPLD). Results: The mean WSG was the only response variable significantly explained by soil variables and charcoal abundance combined. It was significantly negatively associated with soil calcium and Mg content and with charcoal abundance, with soil and charcoal influencing the mean WSG independently. Conclusion: Our study provides evidence that past human disturbances and soil fertility have independently promoted the establishment of light-demanding species in western Central African forests, thereby shedding light on tree community assembly rules in these ecosystems which remain considerably understudied compared to the tropical forests of other continents. © 2020 International Association for Vegetation Science |
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Forest is life, TERRA Teaching and Research Centre, Université de Liège – Gembloux Agro-Bio Tech, Gembloux, Belgium |
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Wiley-Blackwell |
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11009233 (Issn) |
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EcoFoG @ webmaster @ |
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970 |
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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 |
Abbreviated Journal |
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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EcoFoG @ webmaster @ |
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653 |
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Schepaschenko, D.; Chave, J.; Phillips, O.L.; Lewis, S.L.; Davies, S.J.; Réjou-Méchain, M.; Sist, P.; Scipal, K.; Perger, C.; Herault, B.; Labrière, N.; Hofhansl, F.; Affum-Baffoe, K.; Aleinikov, A.; Alonso, A.; Amani, C.; Araujo-Murakami, A.; Armston, J.; Arroyo, L.; Ascarrunz, N.; Azevedo, C.; Baker, T.; Bałazy, R.; Bedeau, C.; Berry, N.; Bilous, A.M.; Bilous, S.Y.; Bissiengou, P.; Blanc, L.; Bobkova, K.S.; Braslavskaya, T.; Brienen, R.; Burslem, D.F.R.P.; Condit, R.; Cuni-Sanchez, A.; Danilina, D.; Del Castillo Torres, D.; Derroire, G.; Descroix, L.; Sotta, E.D.; d'Oliveira, M.V.N.; Dresel, C.; Erwin, T.; Evdokimenko, M.D.; Falck, J.; Feldpausch, T.R.; Foli, E.G.; Foster, R.; Fritz, S.; Garcia-Abril, A.D.; Gornov, A.; Gornova, M.; Gothard-Bassébé, E.; Gourlet-Fleury, S.; Guedes, M.; Hamer, K.C.; Susanty, F.H.; Higuchi, N.; Coronado, E.N.H.; Hubau, W.; Hubbell, S.; Ilstedt, U.; Ivanov, V.V.; Kanashiro, M.; Karlsson, A.; Karminov, V.N.; Killeen, T.; Koffi, J.-C.K.; Konovalova, M.; Kraxner, F.; Krejza, J.; Krisnawati, H.; Krivobokov, L.V.; Kuznetsov, M.A.; Lakyda, I.; Lakyda, P.I.; Licona, J.C.; Lucas, R.M.; Lukina, N.; Lussetti, D.; Malhi, Y.; Manzanera, J.A.; Marimon, B.; Junior, B.H.M.; Martinez, R.V.; Martynenko, O.V.; Matsala, M.; Matyashuk, R.K.; Mazzei, L.; Memiaghe, H.; Mendoza, C.; Mendoza, A.M.; Moroziuk, O.V.; Mukhortova, L.; Musa, S.; Nazimova, D.I.; Okuda, T.; Oliveira, L.C.; Ontikov, P.V.; Osipov, A.F.; Pietsch, S.; Playfair, M.; Poulsen, J.; Radchenko, V.G.; Rodney, K.; Rozak, A.H.; Ruschel, A.; Rutishauser, E.; See, L.; Shchepashchenko, M.; Shevchenko, N.; Shvidenko, A.; Silveira, M.; Singh, J.; Sonké, B.; Souza, C.; Stereńczak, K.; Stonozhenko, L.; Sullivan, M.J.P.; Szatniewska, J.; Taedoumg, H.; Ter Steege, H.; Tikhonova, E.; Toledo, M.; Trefilova, O.V.; Valbuena, R.; Gamarra, L.V.; Vasiliev, S.; Vedrova, E.F.; Verhovets, S.V.; Vidal, E.; Vladimirova, N.A.; Vleminckx, J.; Vos, V.A.; Vozmitel, F.K.; Wanek, W.; West, T.A.P.; Woell, H.; Woods, J.T.; Wortel, V.; Yamada, T.; Nur Hajar, Z.S.; Zo-Bi, I.C. |
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Title |
The Forest Observation System, building a global reference dataset for remote sensing of forest biomass |
Type |
Journal Article |
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2019 |
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Scientific data |
Abbreviated Journal |
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6 |
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198 |
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Forest biomass is an essential indicator for monitoring the Earth's ecosystems and climate. It is a critical input to greenhouse gas accounting, estimation of carbon losses and forest degradation, assessment of renewable energy potential, and for developing climate change mitigation policies such as REDD+, among others. Wall-to-wall mapping of aboveground biomass (AGB) is now possible with satellite remote sensing (RS). However, RS methods require extant, up-to-date, reliable, representative and comparable in situ data for calibration and validation. Here, we present the Forest Observation System (FOS) initiative, an international cooperation to establish and maintain a global in situ forest biomass database. AGB and canopy height estimates with their associated uncertainties are derived at a 0.25 ha scale from field measurements made in permanent research plots across the world's forests. All plot estimates are geolocated and have a size that allows for direct comparison with many RS measurements. The FOS offers the potential to improve the accuracy of RS-based biomass products while developing new synergies between the RS and ground-based ecosystem research communities. |
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Address ![sorted by Address field, ascending order (up)](img/sort_asc.gif) |
FRIM Forest Research Institute of Malaysia, 52109 Kepong, Selangor, Kuala Lumpur, Malaysia |
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Export Date: 21 October 2019 |
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EcoFoG @ webmaster @ |
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889 |
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Lambs, L.; Bompy, F.; Imbert, D.; Corenblit, D.; Dulormne, M. |
![goto web page url](img/www.gif)
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Title |
Seawater and freshwater circulations through coastal forested wetlands on a Caribbean Island |
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Journal Article |
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2015 |
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Water |
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Water |
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7 |
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8 |
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4108-4128 |
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18O/2H stable isotope; Hydrology; Mangrove; Salinity; Swamp forest; Water level |
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Structure and composition of coastal forested wetlands are mainly controlled by local topography and soil salinity. Hydrology plays a major role in relation with tides, seaward, and freshwater inputs, landward. We report here the results of a two-year study undertaken in a coastal plain of the Guadeloupe archipelago (FWI). As elsewhere in the Caribbean islands, the study area is characterized by a micro-tidal regime and a highly seasonal climate. This work aimed at understanding groundwater dynamics and origin (seawater/freshwater) both at ecosystems and stand levels. These hydrological processes were assessed through 18O/16O and 2H/1H isotopic analyses, and from monthly monitoring of water level and soil salinity at five study sites located in mangrove (3) and swamp forest (2). Our results highlight the importance of freshwater budget imbalance during low rainfall periods. Sustained and/or delayed dry seasons cause soil salinity to rise at the mangrove/swamp forest ecotone. As current models on climate change project decreasing rainfall amounts over the inner Caribbean region, one may expect for this area an inland progression of the mangrove forest to the expense of the nearby swamp forest. © 2015 by the authors. |
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Address ![sorted by Address field, ascending order (up)](img/sort_asc.gif) |
Geolab, UMR 6042, CNRS-Université Blaise Pascal, 4 rue Ledru, Clermont-Ferrand Cedex, France |
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Export Date: 8 September 2015 |
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EcoFoG @ webmaster @ |
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621 |
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Longo, M.; Knox, R.G.; Levine, N.M.; Swann, A.L.S.; Medvigy, D.M.; Dietze, M.C.; Kim, Y.; Zhang, K.; Bonal, D.; Burban, B.; Camargo, P.B.; Hayek, M.N.; Saleska, S.R.; Da Silva, R.; Bras, R.L.; Wofsy, S.C.; Moorcroft, P.R. |
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The biophysics, ecology, and biogeochemistry of functionally diverse, vertically and horizontally heterogeneous ecosystems: The Ecosystem Demography model, version 2.2-Part 2: Model evaluation for tropical South America |
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2019 |
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Geoscientific Model Development |
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Geoscientific Model Dev. |
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12 |
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10 |
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4347-4374 |
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The Ecosystem Demography model version 2.2 (ED-2.2) is a terrestrial biosphere model that simulates the biophysical, ecological, and biogeochemical dynamics of vertically and horizontally heterogeneous terrestrial ecosystems. In a companion paper (Longo et al., 2019a), we described how the model solves the energy, water, and carbon cycles, and verified the high degree of conservation of these properties in long-term simulations that include long-term (multi-decadal) vegetation dynamics. Here, we present a detailed assessment of the model's ability to represent multiple processes associated with the biophysical and biogeochemical cycles in Amazon forests. We use multiple measurements from eddy covariance towers, forest inventory plots, and regional remote-sensing products to assess the model's ability to represent biophysical, physiological, and ecological processes at multiple timescales, ranging from subdaily to century long. The ED-2.2 model accurately describes the vertical distribution of light, water fluxes, and the storage of water, energy, and carbon in the canopy air space, the regional distribution of biomass in tropical South America, and the variability of biomass as a function of environmental drivers. In addition, ED-2.2 qualitatively captures several emergent properties of the ecosystem found in observations, specifically observed relationships between aboveground biomass, mortality rates, and wood density; however, the slopes of these relationships were not accurately captured. We also identified several limitations, including the model's tendency to overestimate the magnitude and seasonality of heterotrophic respiration and to overestimate growth rates in a nutrient-poor tropical site. The evaluation presented here highlights the potential of incorporating structural and functional heterogeneity within biomes in Earth system models (ESMs) and to realistically represent their impacts on energy, water, and carbon cycles. We also identify several priorities for further model development. |
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Georgia Institute of Technology, Atlanta, GA, United States |
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Copernicus GmbH |
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Cited By :1; Export Date: 27 October 2019; Correspondence Address: Longo, M.; Harvard UniversityUnited States; email: mdplongo@gmail.com |
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EcoFoG @ webmaster @ |
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Malé, P.-J.G.; Bardon, L.; Besnard, G.; Coissac, E.; Delsuc, F.; Engel, J.; Lhuillier, E.; Scotti-Saintagne, C.; Tinaut, A.; Chave, J. |
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Genome skimming by shotgun sequencing helps resolve the phylogeny of a pantropical tree family |
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Journal Article |
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2014 |
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Molecular Ecology Resources |
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Mol. Ecol. Resour. |
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14 |
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5 |
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966-975 |
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Next-generation sequencing; Organellar genome; Phylogenomics; Tropical trees |
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Whole genome sequencing is helping generate robust phylogenetic hypotheses for a range of taxonomic groups that were previously recalcitrant to classical molecular phylogenetic approaches. As a case study, we performed a shallow shotgun sequencing of eight species in the tropical tree family Chrysobalanaceae to retrieve large fragments of high-copy number DNA regions and test the potential of these regions for phylogeny reconstruction. We were able to assemble the nuclear ribosomal cluster (nrDNA), the complete plastid genome (ptDNA) and a large fraction of the mitochondrial genome (mtDNA) with approximately 1000×, 450× and 120× sequencing depth respectively. The phylogenetic tree obtained with ptDNA resolved five of the seven internal nodes. In contrast, the tree obtained with mtDNA and nrDNA data were largely unresolved. This study demonstrates that genome skimming is a cost-effective approach and shows potential in plant molecular systematics within Chrysobalanaceae and other under-studied groups. © 2014 John Wiley & Sons Ltd. |
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GeT-PlaGe, Genotoul, INRA Auzeville, Castanet-Tolosan, F-31326, France |
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Blackwell Publishing Ltd |
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17550998 (Issn) |
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Export Date: 1 September 2014; Correspondence Address: Malé, P.-J.G.; UMR 5174 Laboratoire Évolution and Diversité Biologique, CNRS, Université Paul Sabatier, ENFA, 118 route de Narbonne, Toulouse, F-31062, France; email: pjg.male@gmail.com |
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EcoFoG @ webmaster @ |
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559 |
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Van Langenhove, L.; Janssens, I.A.; Verryckt, L.; Brechet, L.; Hartley, I.P.; Stahl, C.; Courtois, E.; Urbina, I.; Grau, O.; Sardans, J.; Peguero, G.; Gargallo-Garriga, A.; Peñuelas, J.; Vicca, S. |
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Rapid root assimilation of added phosphorus in a lowland tropical rainforest of French Guiana |
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Journal Article |
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2020 |
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Soil Biology and Biochemistry |
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Soil Biol. Biochem. |
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140 |
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107646 |
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Fertilization; Nitrogen; Phosphorus; Plant root simulator probes; Root system; Tropical forest; Nitrogen; Nitrogen fertilizers; Phosphorus; Plants (botany); Soils; Tropics; Fertilization; Mycorrhizal fungus; N and P fertilizer; P availabilities; Plant root simulators; Root system; Tropical forest; Tropical rain forest; Forestry; Fungi |
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Tree growth on weathered soils in lowland tropical forests is limited by low phosphorous (P) availability. However, nutrient manupulation experiments do not always increase the P content in these trees, which raises the question whether trees are taking up added P. In French Guianese lowland rainforest, we measured changes in nitrogen (N) and P availability before and up to two months after N and P fertilizer addition, in soils with intact root systems and in soils where roots and mycorrhizal fungi were excluded by root exclusion cylinders. When the root system was excluded, P addition increased P availability to a much greater extent and for a longer time than in soils with an intact root system. Soil N dynamics were unaffected by root presence/absence. These results indicate rapid P uptake, but not N uptake, by tree roots, suggesting a very effective P acquisition process in these lowland rainforests. |
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Global Change Research Institute, Czech Academy of Sciences, Czech Republic |
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Elsevier Ltd |
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00380717 (Issn) |
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Export Date: 19 November 2019; Coden: Sbioa; Correspondence Address: Van Langenhove, L.; Centre of Excellence PLECO (Plants and Ecosystems), Department of Biology, University of Antwerp, Wilrijk, Belgium; email: leandro.vanlangenhove@uantwerpen.be |
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EcoFoG @ webmaster @ |
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897 |
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Aguilos, M.; Stahl, C.; Burban, B.; Hérault, B.; Courtois, E.; Coste, S.; Wagner, F.; Ziegler, C.; Takagi, K.; Bonal, D. |
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Interannual and seasonal variations in ecosystem transpiration and water use efficiency in a tropical rainforest |
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Journal Article |
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2018 |
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Forests |
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Forests |
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10 |
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1 |
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Drought; Evapotranspiration; Radiation; Tropical rainforest; Water use efficiency; Atmospheric radiation; Carbon dioxide; Climate change; Drought; Efficiency; Evapotranspiration; Forestry; Heat radiation; Radiation effects; Soil moisture; Tropics; Water supply; Climate condition; Drought conditions; Interannual variability; Mechanistic models; Seasonal variation; Tropical ecosystems; Tropical rain forest; Water use efficiency; Ecosystems |
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Warmer and drier climates over Amazonia have been predicted for the next century with expected changes in regional water and carbon cycles. We examined the impact of interannual and seasonal variations in climate conditions on ecosystem-level evapotranspiration (ET) and water use efficiency (WUE) to determine key climatic drivers and anticipate the response of these ecosystems to climate change. We used daily climate and eddyflux data recorded at the Guyaflux site in French Guiana from 2004 to 2014. ET and WUE exhibited weak interannual variability. The main climatic driver of ET and WUE was global radiation (Rg), but relative extractable water (REW) and soil temperature (Ts) did also contribute. At the seasonal scale, ET and WUE showed a modal pattern driven by Rg, with maximum values for ET in July and August and for WUE at the beginning of the year. By removing radiation effects during water depleted periods, we showed that soil water stress strongly reduced ET. In contrast, drought conditions enhanced radiation-normalized WUE in almost all the years, suggesting that the lack of soil water had a more severe effect on ecosystem evapotranspiration than on photosynthesis. Our results are of major concern for tropical ecosystem modeling because they suggest that under future climate conditions, tropical forest ecosystems will be able to simultaneously adjust CO2 and H2O fluxes. Yet, for tropical forests under future conditions, the direction of change in WUE at the ecosystem scale is hard to predict, since the impact of radiation on WUE is counterbalanced by adjustments to soil water limitations. Developing mechanistic models that fully integrate the processes associated with CO2 and H2O flux control should help researchers understand and simulate future functional adjustments in these ecosystems. |
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Hokkaido University, Sapporo, 060-0808, Japan |
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Mdpi Ag |
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19994907 (Issn) |
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Export Date: 1 February 2019; Correspondence Address: Bonal, D.; Université de Lorraine, AgroParisTech, INRA, UMR SilvaFrance; email: damien.bonal@inra.fr; References: Von Randow, C., Zeri, M., Restrepo-Coupe, N., Muza, M.N., de Gonçalves, L.G.G., Costa, M.H., Araujo, A.C., Saleska, S.R., Interannual variability of carbon and water fluxes in Amazonian forest, Cerrado and pasture sites, as simulated by terrestrial biosphere models (2013) Agric. For. Meteorol, 182-183, pp. 145-155; Duffy, P.B., Brando, P., Asner, G.P., Field, C.B., Projections of future meteorological drought and wet periods in the Amazon (2015) Proc. Natl. Acad. Sci. USA, 112, pp. 13172-13177; Cox, P.M., Betts, R.A., Collins, M., Harris, P.P., Huntingford, C., Jones, C.D., Amazonian forest dieback under climate-carbon cycle projections for the 21st century (2004) Theor. Appl. Climatol, 78, pp. 137-156; Poulter, B., Hattermann, F., Hawkins, E., Zaehle, S., Sitch, S., Restrepo-Coupe, N., Heyder, U., Cramer, W., Robust dynamics of Amazon dieback to climate change with perturbed ecosystem model parameters (2010) Glob. Chang. Biol, 16, pp. 2476-2495; Saleska, S.R., Didan, K., Huete, A.R., Da Rocha, H.R., Amazon forests green-up during 2005 drought (2007) Science, 318, p. 612; Phillips, O.L., Aragão, L.E.O.C., Lewis, S.L., Fisher, J.B., Lloyd, J., López-González, G., Malhi, Y., Quesada, C.A., Drought sensitivity of the amazon rainforest (2009) Science, 323, pp. 1344-1347; Bonal, D., Burban, B., Stahl, C., Wagner, F., Hérault, B., The response of tropical rainforests to drought-Lessons from recent research and future prospects (2016) Ann. For. Sci, 73, pp. 27-44; Wang, K.C., Dickinson, R.E., A review of global terrestrial evapotranspiration: Observation, modeling, climatology, and climatic variability (2012) Rev. Geophys, p. 50; Fisher, R.A., Williams, M., da Costa, A.L., Malhi, Y., da Costa, R.F., Almeida, S., Meir, P., The response of an Eastern Amazonian rain forest to drought stress: Results and modelling analyses from a throughfall exclusion experiment (2007) Glob. Chang. Biol, 13, pp. 2361-2378; Costa, M.H., Biajoli, M.C., Sanches, L., Malhado, A.C.M., Hutyra, L.R., Da Rocha, H.R., Aguiar, R.G., De Araújo, A.C., Atmospheric versus vegetation controls of Amazonian tropical rain forest evapotranspiration: Are the wet and seasonally dry rain forests any different? (2010) J. Geophys. Res. Biogeosci, 115, pp. 1-9; Carswell, F.E., Costa, A.L., Palheta, M., Malhi, Y., Meir, P., Costa, J.D.P.R., Ruivo, M.D.L., Clement, R.J., Seasonality in CO2 and H2O flux at an eastern Amazonian rain forest (2002) J. Geophys. Res. D Atmos, 107, p. 8076; Hasler, N., Avissar, R., What controls evapotranspiration in the Amazon basin? (2007) J. Hydrometeorol, 8, pp. 380-395; Da Rocha, H.R., Manzi, A.O., Cabral, O.M., Miller, S.D., Goulden, M.L., Saleska, S.R., Coupe, N.R., Artaxo, R., Patterns of water and heat flux across a biome gradient from tropical forest to savanna in brazil (2009) J. Geophys. Res. Biogeosci, p. 114; Kim, Y., Knox, R.G., Longo, M., Medvigy, D., Hutyra, L.R., Pyle, E.H., Wofsy, S.C., Moorcroft, P.R., Seasonal carbon dynamics and water fluxes in an Amazon rainforest (2012) Glob. Chang. Biol, 18, pp. 1322-1334; Maeda, E.E., Ma, X., Wagner, F.H., Kim, H., Oki, T., Eamus, D., Huete, A., Evapotranspiration seasonality across the Amazon Basin (2017) Earth Syst. Dyn, 8, pp. 439-454; Farquhar, G.D., Ehleringer, J.R., Hubick, K.T., Carbon isotope discrimination and photosynthesis (1989) Ann. Rev. Plant Physiol, 40, pp. 503-537; Hutyra, L.R., Munger, J.W., Saleska, S.R., Gottlieb, E., Daube, B.C., Dunn, A.L., Amaral, D.F., Wofsy, S.C., Seasonal controls on the exchange of carbon and water in an Amazonian rain forest (2007) J. Geophys. Res. Biogeosci; Negrón Juárez, R.I., Hodnett, M.G., Fu, R., Gouden, M.L., von Randow, C., Control of dry season evapotranspiration over the Amazonian forest as inferred from observation at a Southern Amazon forest site (2007) J. Clim, 20, pp. 2827-2839; Fisher, J.B., Malhi, Y., Bonal, D., Da Rocha, H.R., De Araújo, A.C., Gamo, M., Goulden, M.L., Kondo, H., The land-atmosphere water flux in the tropics (2009) Glob. Chang. Biol; Christoffersen, B.O., Restrepo-Coupe, N., Arain, M.A., Baker, I.T., Cestaro, B.P., Ciais, P., Fisher, J.B., Gulden, L., Mechanisms of water supply and vegetation demand govern the seasonality and magnitude of evapotranspiration in Amazonia and Cerrado (2014) Agric. For. Meteorol, 191, pp. 33-50; Da Costa, A.C.L., Rowland, L., Oliveira, R.S., Oliveira, A.A.R., Binks, O.J., Salmon, Y., Vasconcelos, S.S., Poyatos, R., Stand dynamics modulate water cycling and mortality risk in droughted tropical forest (2018) Glob. Chang. Biol; Huang, M., Piao, S., Sun, Y., Ciais, P., Cheng, L., Mao, J., Poulter, B., Wang, Y., Change in terrestrial ecosystem water-use efficiency over the last three decades (2015) Glob. Chang. Biol; Brienen, R.J.W., Wanek, W., Hietz, P., Stable carbon isotopes in tree rings indicate improved water use efficiency and drought responses of a tropical dry forest tree species (2011) Trees, 25, pp. 103-113; Yu, G., Song, X., Wang, Q., Liu, Y., Guan, D., Yan, J., Sun, X., Wen, X., Water-use efficiency of forest ecosystems in eastern China and its relations to climatic variables (2008) New Phytol, 177, pp. 927-937; Aguilos, M., Hérault, B., Burban, B., Wagner, F., Bonal, D., What drives long-term variations in carbon flux and balance in a tropical rainforest in French Guiana? Agric (2018) For. Meteorol, pp. 253-254; Bonal, D., Bosc, A., Ponton, S., Goret, J.Y., Burban, B.T., Gross, P., Bonnefond, J.M., Epron, D., Impact of severe dry season on net ecosystem exchange in the Neotropical rainforest of French Guiana (2008) Glob. Chang. Biol; Aubinet, M., Grelle, A., Ibrom, A., Rannik, U., Moncrieff, J.B., Foken, T., Kowalski, A.S., Bernhofer, C., Estimates of the annual net carbon and water exchange of forests: The Euroflux methodology (2000) Adv. Ecol. Res, 30, pp. 113-175; Wagner, F., Hérault, B., Stahl, C., Bonal, D., Rossi, V., Modeling water availability for trees in tropical forests (2011) Agric. For. Meteorol, 151, pp. 1202-1213; Kuglitsch, F.G., Reichstein, M., Beer, C., Carrara, A., Ceulemans, R., Granier, A., Janssens, I.A., Loustau, D., Characterisation of ecosystem water-use efficiency of european forests from eddy covariance measurements (2008) Biogeosci. Discuss, 5, pp. 4481-4519; Dekker, S.C., Groenendijk, M., Booth, B.B.B., Huntingford, C., Cox, P.M., Spatial and temporal variations in plant water-use efficiency inferred from tree-ring, eddy covariance and atmospheric observations (2016) Earth Syst. Dyn, 7, pp. 525-533; Yang, Y., Guan, H., Batelaan, O., McVicar, T.R., Long, D., Piao, S., Liang, W., Simmons, C.T., Contrasting responses of water use efficiency to drought across global terrestrial ecosystems (2016) Sci. Rep, 6, p. 23284; Granier, A., Bréda, N., Biron, P., Villette, S., A lumped water balance model to evaluate duration and intensity of drought constraints in forest stands (1999) Ecol. Model, 116, pp. 269-283; Kume, T., Takizawa, H., Yoshifuji, N., Tanaka, K., Tantasirin, C., Tanaka, N., Suzuki, M., Impact of soil drought on sap flow and water status of evergreen trees in a tropical monsoon forest in northern Thailand (2007) For. Ecol. Manag, 238, pp. 220-230; Xiao, J., Sun, G., Chen, J., Chen, H., Chen, S., Dong, G., Gao, S., Han, S., Carbon fluxes, evapotranspiration, and water use efficiency of terrestrial ecosystems in China (2013) Agric. For. Meteorol; Boese, S., Jung, M., Carvalhais, N., Reichstein, M., The importance of radiation for semi-empirical water-use efficiency models (2017) Biogeosciences, 14, pp. 3015-3026; Bonal, D., Ponton, S., Le Thiec, D., Richard, B., Ningre, N., Hérault, B., Ogée, J., Sabatier, D., Leaf functional response to increasing atmospheric CO2 concentrations over the last century in two northern Amazonian tree species: An historical δ13C and δ18O approach using herbarium samples (2011) Plant Cell Environ, 34, pp. 1332-1344; Wagner, F., Rossi, V., Stahl, C., Bonal, D., Hérault, B., Water availability is the main climate driver of neotropical tree growth (2012) PLoS ONE, 7; Van der Molen, M.K., Dolman, A.J., Ciais, P., Eglin, T., Gobron, N., Law, B.E., Meir, P., Reichstein, M., Drought and ecosystem carbon cycling (2011) Agric. For. Meteorol, 151, pp. 765-773; Allen, C.D., Macalady, A.K., Chenchouni, H., Bachelet, D., McDowell, N., Vennetier, M., Kitzberger, T., Hogg, E.H., A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forests (2010) For. Ecol. Manag, 259, pp. 660-684; Da Rocha, H.R., Goulden, M.L., Miller, S.D., Menton, M.C., Pinto, L.D., De Freitas, H.C., Seasonality of water and heat fluxes over a tropical forest in eastern Amazonia (2004) Ecol. Appl, 14, pp. 22-32; Baldocchi, D., Falge, E., Gu, L., Olson, R., Hollinger, D., Running, S., Anthoni, P., Evans, R., FLUXNET: A New tool to study the temporal and spatial variability of ecosystem-scale carbon dioxide, water vapor, and energy flux densities (2001) Bull. Am. Meteorol. Soc, 82, pp. 2415-2434; Stahl, C., Hérault, B., Rossi, V., Burban, B., Bréchet, C., Bonal, D., Depth of soil water uptake by tropical rainforest trees during dry periods: Does tree dimension matter? (2013) Oecologia, 173, pp. 1191-1201; Nepstad, D.C., De Carvalho, C.R., Davidson, E.A., Jipp, P.H., Lefebvre, P.A., Negreiros, G.H., Da Silva, E.D., Vieira, S., The role of deep roots in the hydrological and carbon cycles of Amazonian forests and pastures (1994) Nature; Lee, J.-E., Boyce, K., Impact of the hydraulic capacity of plants on water and carbon fluxes in tropical South America (2010) J. Geophys. Res; Xiao, X., Zhang, Q., Saleska, S., Hutyra, L., De Camargo, P., Wofsy, S., Frolking, S., Moore, B., Satellite-based modeling of gross primary production in a seasonally moist tropical evergreen forest (2005) Remote Sens. Environ, 94, pp. 105-122; Wagner, F.H., Hérault, B., Bonal, D., Stahl, C., Anderson, L.O., Baker, T.R., Becker, G.S., Botosso, P.C., Climate seasonality limits leaf carbon assimilation and wood productivity in tropical forests (2016) Biogeosciences, 13, pp. 2537-2562; Stahl, C., Burban, B., Wagner, F., Goret, J.-Y., Bompy, F., Bonal, D., Influence of Seasonal Variations in Soil Water Availability on Gas Exchange of Tropical Canopy Trees (2013) Biotropica, 45, pp. 155-164; Maréchaux, I., Bonal, D., Bartlett, M.K., Burban, B., Coste, S., Courtois, E.A., Dulormne, M., Mirabel, A., Dry-season decline in tree sapflux is correlated with leaf turgor loss point in a tropical rainforest (2018) Funct. Ecol, 32, pp. 2285-2297; Chaves, M.M., Maroco, J.P., Pereira, J.S., Understanding plant responses to drought-from genes to the whole plant (2003) Funct. Plant Biol, 30, pp. 239-264 |
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EcoFoG @ webmaster @ |
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856 |
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Permanent link to this record |