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Perrin, A.-S.; Fujisaki, K.; Petitjean, C.; Sarrazin, M.; Godet, M.; Garric, B.; Horth, J.-C.; Balbino, L.C.; Filho, A.S.; de Almeida Machado, P.L.O.; Brossard, M. |
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Conversion of forest to agriculture in Amazonia with the chop-and-mulch method: Does it improve the soil carbon stock? |
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Journal Article |
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2014 |
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Agriculture, Ecosystems and Environment |
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Agric. Ecosyst. Environ. |
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184 |
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101-114 |
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Annual crops; Brachiaria; Deforestation; Fire-free; French Guiana; No-tillage |
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Fire-free forest conversion with organic inputs as an alternative to slash-and-burn could improve agro-ecosystem sustainability. We assessed soil carbon mass changes in a sandy-clayey and well-drained soil in French Guiana after forest clearing by the chop-and-mulch method and crop establishment. At the experimental site of Combi, native forest was cut down in October 2008; woody biomass was chopped and incorporated into the top 20cm of soil. After about one year of legume and grass cover, three forms of land management were compared: grassland (Urochloa ruziziensis), maize/soybean crop rotation with disk tillage and in direct seeding without tillage. There were four replicates. We measured 14.16kgm-2 of carbon in 2mm-sieved soil down to 2m depth for the initial forest. Forest clearing did not induce significant soil compaction; neither did any specific agricultural practice. In converted soils, C stocks were measured in the 0-30cm layer after each crop for three years. Carbon mass changes for soil fractions <2mm (soil C stock) and >2mm (soil C pool) in the 0-5, 5-10, 10-20 and 20-30cm soil layers were assessed on an equivalent soil mass basis. One year and 1.5 years after deforestation, higher C stocks (+0.64 to 1.16kgCm-2yr-1) and C pools (+0.52 to 0.90kgCm-2yr-1) were measured in converted soils, compared to those of the forest into the top 30cm of soil. However, the masses of carbon in these converted soils declined later. The highest rates of carbon decrease were measured between 1.5 and 2 years after forest conversion in the <2mm soil fraction, from 0.46kgCm-2yr-1 (in grassland soils) to 0.71kgCm-2yr-1 (in cropland under no tillage). The carbon pool declined during the third year at rates of 0.41kgCm-2yr-1 (cropland under disk tillage) to 0.76kgCm-2yr-1 (grassland soils). Three years after forest conversion, C masses in the top 30cm of soils for grassland showed similar values than for forest. In comparison, the carbon stock in cropped soils managed under no tillage in direct seeding (without mulch) was significantly 17% and 16% lower than in forest and grassland soils, respectively. None of the studied agricultural practices succeeded in accumulating carbon from the chopped forest biomass. © 2013 Elsevier B.V. |
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EMBRAPA Arroz e Feijao, Cx Postal 179, CEP 75375-000 Santo Antonio de Goias, GO, Brazil |
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Export Date: 2 January 2014; Source: Scopus; Coden: Aeend; doi: 10.1016/j.agee.2013.11.009 |
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Groc, S.; Delabie, J.H.C.; Fernández, F.; Leponce, M.; Orivel, J.; Silvestre, R.; Vasconcelos, H.L.; Dejean, A. |
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Leaf-litter ant communities in a pristine Guianese rainforest: stable functional structure versus high species turnover |
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2013 |
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Myrmecological News |
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Myrmecol. News |
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19 |
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43-51 |
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Leroy, C.; Gril, E.; Si Ouali, L.; Coste, S.; Gérard, B.; Maillard, P.; Mercier, H.; Stahl, C. |
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Water and nutrient uptake capacity of leaf-absorbing trichomes vs. roots in epiphytic tank bromeliads |
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Journal Article |
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2019 |
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Environmental and Experimental Botany |
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Environ. Exp. Bot. |
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163 |
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112-123 |
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15 N labelling; Carbon metabolism; Nutrient uptake; Plant performance; Tank bromeliad; Water status; Aechmea |
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The water and nutrient uptake mechanisms used by vascular epiphytes have been the subject of a few studies. While leaf absorbing trichomes (LATs) are the main organ involved in resource uptake by bromeliads, little attention has been paid to the absorbing role of epiphytic bromeliad roots. This study investigates the water and nutrient uptake capacity of LATs vs. roots in two epiphytic tank bromeliads Aechmea aquilega and Lutheria splendens. The tank and/or the roots of bromeliads were watered, or not watered at all, in different treatments. We show that LATs and roots have different functions in resource uptake in the two species, which we mainly attributed to dissimilarities in carbon acquisition and growth traits (e.g., photosynthesis, relative growth rate, non-structural carbohydrates, malate), to water relation traits (e.g., water and osmotic potentials, relative water content, hydrenchyma thickness) and nutrient uptake (e.g., 15 N-labelling). While the roots of A. aquilega did contribute to water and nutrient uptake, the roots of L. splendens were less important than the role played by the LATs in resource uptake. We also provide evidenced for a synergistic effect of combined watering of tank and root in the Bromelioideae species. These results call for a more complex interpretation of LATs vs. roots in resource uptake in bromeliads. © 2019 Elsevier B.V. |
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INRA, UMR EcoFoG, CNRS, CIRAD, AgroParisTech, Université des Antilles, Université de Guyane, Kourou, 97310, France |
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Elsevier B.V. |
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00988472 (Issn) |
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EcoFoG @ webmaster @ |
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871 |
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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 |
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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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Nature Publishing Group |
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00280836 (Issn) |
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872 |
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Salhi, L.; Nait-Rabah, O.; Deyrat, C.; Roos, C. |
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Numerical Modeling of Single Helical Pile Behavior under Compressive Loading in Sand |
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Journal Article |
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2013 |
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Electronic Journal of Geotechnical Engineering |
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Electron. J. Geotech. Eng. |
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18 |
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Bundle T |
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4119-4338 |
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helical pile; finite element method; failure mechanisms; sand |
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The present research deals with helical piles behavior in cohesionless soil through finite element modeling. An approach of modeling of the screw-pile geometry has been proposed through the Finite Element Analysis (FEA) computer program Plaxis. The numerical results are compared with measurements from large scale test and the bearing capacity has been estimated using both cylindrical and individual bearing model. Moreover, different failure criterions have been applied to estimate the ultimate capacity. The effect of spacing ratio (S/Dh) on the screw-pile behavior has been further studied. It has found that results from the model fit the field results. Through the study of the load transfer mechanism, the transition from cylindrical shear to individual plate behavior occurs at a value of spacing ratio (1.5 to 2). |
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Laboratoire des matériaux et molécules en milieu amazonien, EcoFoG-Université des Antilles-Guyane, 97351 Cayenne, French Guiana |
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Houel, E.; Rodrigues, A.M.S.; Jahn-Oyac, A.; Bessière, J.-M.; Eparvier, V.; Deharo, E.; Stien, D. |
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In vitro antidermatophytic activity of Otacanthus azureus (Linden) Ronse essential oil alone and in combination with azoles |
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2014 |
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Journal of Applied Microbiology |
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J. Appl. Microbiol. |
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116 |
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2 |
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288-294 |
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Antifungal activity; Azoles; Dermatophytes; Essential oil; Otacanthus azureus; Synergy |
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Aims: We determined the chemical composition and investigated the antifungal activity of Otacanthus azureus (Linden) Ronse essential oil (EO) against a range of dermatophytes alone or in combination with azole antifungals. Methods and Results: Aerial parts of the plant were steam-distilled and the obtained oil was analysed by gas chromatography/mass spectrometry and 1H-NMR. It was shown to be largely composed of sesquiterpenes, with the main component being β-copaen-4-α-ol. Using broth microdilution techniques, this oil was found to have remarkable in vitro antifungal activities. Minimum inhibitory concentrations as low as 4 μg ml-1 were recorded. The analysis of the combined effect of the O. azureus EO with azoles using chequerboard assays revealed a synergism between the EO and ketoconazole, fluconazole or itraconazole against Trichophyton mentagrophytes. Notably, the O. azureus essential oil showed low cytotoxicity to VERO cells. Conclusions: The O. azureus essential oil alone or in combination with azoles is a promising antifungal agent in the treatment for human dermatomycoses caused by filamentous fungi. Significance and Impact of the Study: There is much interest in the study of essential oils for the discovery of new antimicrobial drugs. This study has highlighted the antidermatophytic activity of the O. azureus EO. © 2013 The Society for Applied Microbiology. |
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Institut de Recherche pour le Développement (IRD), UMR 152 Pharma-DEV, Toulouse, France |
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Export Date: 9 February 2014; Source: Scopus; Coden: Jamif; Language of Original Document: English; Correspondence Address: Houël, E.; CNRS – UMR Ecologie des Forêts de Guyane (EcoFoG), Institut Pasteur de la Guyane, 23 Avenue Pasteur, BP6010, 97306 Cayenne Cedex, French Guiana; email: emeline.houel@ecofog.gf |
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Woolfit, M.; Iturbe-Ormaetxe, I.; Brownlie, J.C.; Walker, T.; Riegler, M.; Seleznev, A.; Popovici, J.; Rancès, E.; Wee, B.A.; Pavlides, J.; Sullivan, M.J.; Beatson, S.A.; Lane, A.; Sidhu, M.; McMeniman, C.J.; McGraw, E.A.; O'Neill, S.L. |
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Genomic evolution of the pathogenic Wolbachia strain, wMelPop |
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2013 |
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Genome Biology and Evolution |
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Genome Biolog. Evol. |
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5 |
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11 |
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2189-2204 |
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Endosymbiont; Evolution; Genomics; Wolbachia |
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Most strains of the widespread endosymbiotic bacterium Wolbachia pipientis are benign or behave as reproductive parasites. The pathogenic strain wMelPop is a striking exception, however: it overreplicates in its insect hosts and causes severe life shortening. The mechanism of this pathogenesis is currently unknown. We have sequenced the genomes of three variants of wMelPop and of the closely related nonpathogenic strain wMelCS. We show that the genomes of wMelCS and wMelPop appear to be identical in the nonrepeat regions of the genome and differ detectably only by the triplication of a 19-kb region that is unlikely to be associated with life shortening, demonstrating that dramatic differences in the host phenotype caused by this endosymbiont may be the result of only minor genetic changes. We also compare the genomes of the original wMelPop strain from Drosophila melanogaster and two sequentialderivatives, wMelPop-CLA and wMelPop-PGYP. To develop wMelPop as a novel biocontrol agent, it was first transinfected into and passaged in mosquito cell lines for approximately 3.5 years, generating wMelPop-CLA. This cell line-passaged strain was then transinfected into Aedesaegypti mosquitoes, creating wMelPop-PGYP,which wassequenced after 4yearsin the insecthost. We observe a rapid burst of genomic changes during cell line passaging, but no further mutations were detected after transinfection into mosquitoes, indicating either that host preadaptation had occurred in cell lines, that cell lines are a more selectively permissive environment than animal hosts, or both. Our results provide valuable data on the rates of genomic and phenotypic change in Wolbachia associated with host shifts over short time scales. © The Author(s) 2013. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. |
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Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia |
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Export Date: 9 February 2014; Source: Scopus; Language of Original Document: English; Correspondence Address: O'Neill, S.L.; School of Biological Sciences, Monash University, Clayton, VIC, Australia; email: scott.oneill@monash.edu; Funding Details: NIH, National Institutes of Health |
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Rockwell, C.A.; Kainer, K.A.; d'Oliveira, M.V.N.; Staudhammer, C.L.; Baraloto, C. |
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Logging in bamboo-dominated forests in southwestern Amazonia: Caveats and opportunities for smallholder forest management |
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Journal Article |
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2014 |
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Forest Ecology and Management |
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For. Ecol. Manage. |
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315 |
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202-210 |
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Bamboo; Community forest management; Guadua; Logging; Timber management; Tropical forest |
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Guadua sarcocarpa and Guadua weberbaueri (Poaceae: Bambuseae) have a negative influence on tree regeneration and recruitment in bamboo-dominated forests of southwestern Amazonia. The lack of advanced regeneration and sparse canopy in this forest type present a considerable challenge for developing sustainable timber management plans. We conducted field studies in the Porto Dias Agroextractive Settlement Project in Acre, Brazil to assess influences of logging in bamboo-dominated forest sites. Taxonomic composition, stand structure, aboveground biomass, commercial timber volume, and commercial tree seedling and bamboo culm density were compared between five logged vs. unlogged sites in different landholdings, using modified 0.5. ha Gentry plots. No differences in taxonomic composition, aboveground biomass, adult and juvenile stem density, or woody seedling and bamboo culm density were detected between paired logged and unlogged sites. Commercial timber volume, however, was reduced by almost two-thirds in logged plots, suggesting that long-term timber management goals in this forest type are compromised since so few future crop trees remained onsite. Our findings indicate that in order to maximize local management objectives, community forest managers must approach logging in bamboo-dominated forests with caution. We suggest an integration of non-timber forest product extraction with low harvest intensity and low-impact logging, tending of natural regeneration, and diversification of commercial species. © 2014 Elsevier B.V. |
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INRA, UMR Ecologie des Forêts de Guyane, 97387 Kourou Cedex, French Guiana |
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Export Date: 15 February 2014; Source: Scopus; Coden: Fecmd; Language of Original Document: English; Correspondence Address: Rockwell, C.A.; School of Forest Resources and Conservation, University of Florida, Gainesville, FL 32611, United States; email: rockwell_cara@yahoo.com; Funding Details: DGE-0221599, NSF, National Science Foundation |
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Rowland, L.; Hill, T.C.; Stahl, C.; Siebicke, L.; Burban, B.; Zaragoza-Castells, J.; Ponton, S.; Bonal, D.; Meir, P.; Williams, M. |
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Evidence for strong seasonality in the carbon storage and carbon use efficiency of an Amazonian forest |
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2014 |
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Global Change Biology |
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Global Change Biol. |
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20 |
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3 |
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979-991 |
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Carbon use efficiency; Dalec; Data assimilation; Ecosystem respiration; French Guiana; Seasonal carbon fluxes; Tropical forest |
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The relative contribution of gross primary production and ecosystem respiration to seasonal changes in the net carbon flux of tropical forests remains poorly quantified by both modelling and field studies. We use data assimilation to combine nine ecological time series from an eastern Amazonian forest, with mass balance constraints from an ecosystem carbon cycle model. The resulting analysis quantifies, with uncertainty estimates, the seasonal changes in the net carbon flux of a tropical rainforest which experiences a pronounced dry season. We show that the carbon accumulation in this forest was four times greater in the dry season than in the wet season and that this was accompanied by a 5% increase in the carbon use efficiency. This seasonal response was caused by a dry season increase in gross primary productivity, in response to radiation and a similar magnitude decrease in heterotrophic respiration, in response to drying soils. The analysis also predicts increased carbon allocation to leaves and wood in the wet season, and greater allocation to fine roots in the dry season. This study demonstrates implementation of seasonal variations in parameters better enables models to simulate observed patterns in data. In particular, we highlight the necessity to simulate the seasonal patterns of heterotrophic respiration to accurately simulate the net carbon flux seasonal tropical forest. © 2013 The Authors Global Change Biology Published by John Wiley & Sons Ltd. |
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Research School of Biology, Division of Plant Sciences, Australian National University, Canberra, ACT, 0200, Australia |
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Cited By (since 1996):1; Export Date: 24 February 2014; Source: Scopus; Language of Original Document: English; Correspondence Address: Rowland, L.; School of Geosciences, University of Edinburgh, Edinburgh, EH9 3JN, United Kingdom; email: lucy.rowland@ed.ac.uk; Funding Details: FT110100457, ARC, Australian Research Council; Funding Details: NE/F002149/1, NERC, Natural Environment Research Council; Funding Details: NE/J011002/1, NERC, Natural Environment Research Council |
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Lamarre, G.P.A.; Mendoza, I.; Fine, P.V.A.; Baraloto, C. |
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Leaf synchrony and insect herbivory among tropical tree habitat specialists |
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2014 |
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Plant Ecology |
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Plant Ecol. |
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215 |
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2 |
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209-220 |
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Escape; French Guiana; Herbivorous insects; Phenology; Resource availability; Time lag |
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Growth defense tradeoff theory predicts that plants in low-resource habitats invest more energy in defense mechanisms against natural enemies than growth, whereas plants in high-resource habitats can afford higher leaf loss rates. A less-studied defense against herbivores involves the synchrony of leaf production, which can be an effective defense strategy if leaf biomass production exceeds the capacity of consumption by insects. The aim of this study was to determine whether leaf synchrony varied across habitats with different available resources and whether insects were able to track young leaf production among tree habitat specialists in a tropical forest of French Guiana. We predicted that high-resource habitats would exhibit more synchrony in leaf production due to the low cost and investment to replace leaf tissue. We also expected closer patterns of leaf synchrony and herbivory within related species, assuming that they shared herbivores. We simultaneously monitored leaf production and herbivory rates of five pairs of tree species, each composed of a specialist of terra firme or white-sand forests within the same lineage. Our prediction was not supported by the strong interaction of habitat and lineage for leaf synchrony within individuals of the same species; although habitat specialists differed in leaf synchrony within four of five lineages, the direction of the effect was variable. All species showed short time lags for the correlation between leaf production and herbivory, suggesting that insects are tightly tracking leaf production, especially for the most synchronous species. Leaf synchrony may provide an important escape defense against herbivores, and its expression appears to be constrained by both evolutionary history and environmental factors. © 2014 Springer Science+Business Media Dordrecht. |
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Department of Biology, University of Florida, Gainesville, FL, 32611, United States |
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13850237 (Issn) |
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Export Date: 24 February 2014; Source: Scopus; Coden: Plecf; Language of Original Document: English; Correspondence Address: Lamarre, G. P. A.; Université Antilles Guyane, UMR Ecologie des Forêts de Guyane, 97310 Kourou, French Guiana; email: greglamarre973@gmail.com; Funding Details: DEB-0743103/0743800, NSF, National Science Foundation |
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