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Esquivel-Muelbert, A.; Baker, T.R.; Dexter, K.G.; Lewis, S.L.; Brienen, R.J.W.; Feldpausch, T.R.; Lloyd, J.; Monteagudo-Mendoza, A.; Arroyo, L.; Álvarez-Dávila, E.; Higuchi, N.; Marimon, B.S.; Marimon-Junior, B.H.; Silveira, M.; Vilanova, E.; Gloor, E.; Malhi, Y.; Chave, J.; Barlow, J.; Bonal, D.; Davila Cardozo, N.; Erwin, T.; Fauset, S.; Hérault, B.; Laurance, S.; Poorter, L.; Qie, L.; Stahl, C.; Sullivan, M.J.P.; ter Steege, H.; Vos, V.A.; Zuidema, P.A.; Almeida, E.; Almeida de Oliveira, E.; Andrade, A.; Vieira, S.A.; Aragão, L.; Araujo-Murakami, A.; Arets, E.; Aymard C, G.A.; Baraloto, C.; Camargo, P.B.; Barroso, J.G.; Bongers, F.; Boot, R.; Camargo, J.L.; Castro, W.; Chama Moscoso, V.; Comiskey, J.; Cornejo Valverde, F.; Lola da Costa, A.C.; del Aguila Pasquel, J.; Di Fiore, A.; Fernanda Duque, L.; Elias, F.; Engel, J.; Flores Llampazo, G.; Galbraith, D.; Herrera Fernández, R.; Honorio Coronado, E.; Hubau, W.; Jimenez-Rojas, E.; Lima, A.J.N.; Umetsu, R.K.; Laurance, W.; Lopez-Gonzalez, G.; Lovejoy, T.; Aurelio Melo Cruz, O.; Morandi, P.S.; Neill, D.; Núñez Vargas, P.; Pallqui Camacho, N.C.; Parada Gutierrez, A.; Pardo, G.; Peacock, J.; Peña-Claros, M.; Peñuela-Mora, M.C.; Petronelli, P.; Pickavance, G.C.; Pitman, N.; Prieto, A.; Quesada, C.; Ramírez-Angulo, H.; Réjou-Méchain, M.; Restrepo Correa, Z.; Roopsind, A.; Rudas, A.; Salomão, R.; Silva, N.; Silva Espejo, J.; Singh, J.; Stropp, J.; Terborgh, J.; Thomas, R.; Toledo, M.; Torres-Lezama, A.; Valenzuela Gamarra, L.; van de Meer, P.J.; van der Heijden, G.; van der Hout, P.; Vasquez Martinez, R.; Vela, C.; Vieira, I.C.G.; Phillips, O.L. |
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Title |
Compositional response of Amazon forests to climate change |
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Journal Article |
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Year |
2019 |
Publication |
Global Change Biology |
Abbreviated Journal  |
Global Change Biol. |
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Volume |
25 |
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1 |
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39-56 |
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bioclimatic niches; climate change; compositional shifts; functional traits; temporal trends; tropical forests; bioclimatology; climate change; floristics; lowland environment; niche; temporal variation; tropical forest; Amazonia; carbon dioxide; water; biodiversity; Brazil; classification; climate change; ecosystem; forest; physiology; season; tree; tropic climate; Biodiversity; Brazil; Carbon Dioxide; Climate Change; Ecosystem; Forests; Seasons; Trees; Tropical Climate; Water |
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Most of the planet's diversity is concentrated in the tropics, which includes many regions undergoing rapid climate change. Yet, while climate-induced biodiversity changes are widely documented elsewhere, few studies have addressed this issue for lowland tropical ecosystems. Here we investigate whether the floristic and functional composition of intact lowland Amazonian forests have been changing by evaluating records from 106 long-term inventory plots spanning 30 years. We analyse three traits that have been hypothesized to respond to different environmental drivers (increase in moisture stress and atmospheric CO 2 concentrations): maximum tree size, biogeographic water-deficit affiliation and wood density. Tree communities have become increasingly dominated by large-statured taxa, but to date there has been no detectable change in mean wood density or water deficit affiliation at the community level, despite most forest plots having experienced an intensification of the dry season. However, among newly recruited trees, dry-affiliated genera have become more abundant, while the mortality of wet-affiliated genera has increased in those plots where the dry season has intensified most. Thus, a slow shift to a more dry-affiliated Amazonia is underway, with changes in compositional dynamics (recruits and mortality) consistent with climate-change drivers, but yet to significantly impact whole-community composition. The Amazon observational record suggests that the increase in atmospheric CO 2 is driving a shift within tree communities to large-statured species and that climate changes to date will impact forest composition, but long generation times of tropical trees mean that biodiversity change is lagging behind climate change. |
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Museu Paraense Emílio Goeldi, Pará, Brazil |
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Blackwell Publishing Ltd |
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13541013 (Issn) |
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Cited By :21; Export Date: 6 January 2020; Correspondence Address: Esquivel-Muelbert, A.; School of Geography, University of LeedsUnited Kingdom; email: adriane.esquivel@gmail.com |
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EcoFoG @ webmaster @ |
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905 |
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Bodin, S.C.; Scheel-Ybert, R.; Beauchene, J.; Molino, J.-F.; Bremond, L. |
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CharKey: An electronic identification key for wood charcoals of French Guiana |
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Journal Article |
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Year |
2019 |
Publication |
IAWA Journal |
Abbreviated Journal |
Iawa J. |
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40 |
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1 |
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75-91 |
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anthracology; Charcoal anatomy; computeraided identification; Note: Supplementary material can be accessed in the online edition of this journal via brill.com/iawa.; tropical flora; Xper 2 |
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Tropical tree floras are highly diverse and many genera and species share similar anatomical patterns, making the identification of tropical wood charcoal very difficult. Appropriate tools to characterize charcoal anatomy are thus needed to facilitate and improve identification in such species-rich areas. This paper presents the first computer-aided identification key designed for charcoals from French Guiana, based on the wood anatomy of 507 species belonging to 274 genera and 71 families, which covers respectively 28%, 67% and 86% of the tree species, genera and families currently listed in this part of Amazonia. Species of the same genus are recorded together except those described under a synonym genus in Détienne et al. (1982) that were kept separately. As a result, the key contains 289 'items' and mostly aims to identify charcoals at the genus level. It records 26 anatomical features leading to 112 feature states, almost all of which are illustrated by SEM photographs of charcoal. The descriptions were mostly taken from Détienne et al.'s guidebook on tropical woods of French Guiana (1982) and follow the IAWA list of microscopic features for hardwood identification (Wheeler et al. 1989). Some adjustments were made to a few features and those that are unrelated to charcoal identification were excluded. The whole tool, named CharKey, contains the key itself and the associated database including photographs. It can be downloaded on Figshare at https://figshare.com/s/d7d40060b53d2ad60389 (doi: 10.6084/m9.figshare.6396005). CharKey is accessible using the free software Xper 2 , specifically conceived for taxonomic description and computer aided-identification. |
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Ecole Pratique des Hautes Etudes, PSL Research University, Paris, France |
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Brill Academic Publishers |
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09281541 (Issn) |
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EcoFoG @ webmaster @ |
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864 |
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Ruiz-González, M.X.; Leroy, C.; Dejean, A.; Gryta, H.; Jargeat, P.; Carrión, A.D.A.; Orivel, J. |
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Do host plant and associated ant species affect microbial communities in myrmecophytes? |
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Journal Article |
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Year |
2019 |
Publication |
Insects |
Abbreviated Journal |
Insects |
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10 |
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11 |
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391 |
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Allomerus decemarticulatus; Allomerus octoarticulatus; Azteca sp; Cf; Cordia nodosa; Depilis; Domatia; Hirtella physophora; Microbial diversity |
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Ant-associated microorganisms can play crucial and often overlooked roles, and given the diversity of interactions that ants have developed, the study of the associated microbiomes is of interest. We focused here on specialist plant-ant species of the genus Allomerus that grow a fungus to build galleries on their host-plant stems. Allomerus-inhabited domatia, thus, might be a rich arena for microbes associated with the ants, the plant, and the fungus. We investigated the microbial communities present in domatia colonised by four arboreal ants: Allomerus decemarticulatus, A. octoarticulatus, A. octoarticulatus var. demerarae, and the non-fungus growing plant-ant Azteca sp. cf. depilis, inhabiting Hirtella physophora or Cordia nodosa in French Guiana. We hypothesized that the microbial community will differ among these species. We isolated microorganisms from five colonies of each species, sequenced the 16S rRNA or Internal TranscribedSpacer (ITS) regions, and described both the alpha and beta diversities. We identified 69 microbial taxa, which belong to five bacterial and two fungal phyla. The most diverse phyla were Proteobacteria and Actinobacteria. The microbial community of Azteca cf. depilis and Allomerus spp. differed in composition and richness. Geographical distance affected microbial communities and richness but plant species did not. Actinobacteria were only associated with Allomerus spp. |
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Biodiversity Genomics Team, Plant Ecophysiology & Evolution Group, Guangxi Key Laboratory of Forest Ecology and Conservation, College of Forestry, Daxuedonglu 100, Nanning, Guangxi 530005, China |
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Mdpi Ag |
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20754450 (Issn) |
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Export Date: 18 November 2019; Correspondence Address: Ruiz-González, M.X.; Departamento de Ciencias Biológicas, Universidad Técnica Particular de Loja, San Cayetano Alto s/n, Ecuador; email: marioxruizgonzalez@gmail.com |
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EcoFoG @ webmaster @ |
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896 |
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Sprenger, P.P.; Hartke, J.; Feldmeyer, B.; Orivel, J.; Schmitt, T.; Menzel, F. |
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Influence of Mutualistic Lifestyle, Mutualistic Partner, and Climate on Cuticular Hydrocarbon Profiles in Parabiotic Ants |
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Journal Article |
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Year |
2019 |
Publication |
Journal of Chemical Ecology |
Abbreviated Journal |
J Chem Ecol |
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45 |
Issue |
9 |
Pages |
741-754 |
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A vital trait in insects is their cuticular hydrocarbon (CHC) profile, which protects the insect against desiccation and serves in chemical communication. Due to these functions, CHC profiles are shaped by both climatic conditions and biotic interactions. Here, we investigated CHC differentiation in the neotropical parabiotic ant species Crematogaster levior and Camponotus femoratus, which mutualistically share a nest. Both consist of two cryptic species each (Cr. levior A and B and Ca. femoratus PAT and PS) that differ genetically and possess strongly different CHC profiles. We characterized and compared CHC profiles of the four cryptic species in detail. Our results suggest that Cr. levior A, Ca. femoratus PAT and Ca. femoratus PS adapted their CHC profiles to the parabiotic lifestyle by producing longer-chain CHCs. At the same time, they changed their major CHC classes, and produce more alkadienes and methyl-branched alkenes compared to Cr. levior B or non-parabiotic species. The CHC profiles of Cr. levior B were more similar to related, non-parabiotic species of the Orthocrema clade than Cr. levior A, and the chain lengths of B were similar to the reconstructed ancestral state. Signals of both the parabiotic partner (biotic conditions) and climate (abiotic conditions) were found in the CHC profiles of all four cryptic species. Our data suggest that mutualisms shaped the CHC profiles of the studied species, in particular chain length and CHC class composition. Beside this, signals of the parabiotic partners indicate potential impacts of biotic interactions, via chemical mimicry or chemical camouflage. |
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1573-1561 |
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EcoFoG @ webmaster @ Sprenger2019 |
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894 |
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Ciminera, M.; Auger-Rozenberg, M.-A.; Caron, H.; Herrera, M.; Scotti-Saintagne, C.; Scotti, I.; Tysklind, N.; Roques, A. |
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Genetic Variation and Differentiation of Hylesia metabus (Lepidoptera: Saturniidae): Moths of Public Health Importance in French Guiana and in Venezuela |
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Journal Article |
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Year |
2019 |
Publication |
Journal of medical entomology |
Abbreviated Journal |
J. Med. Entomol. |
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56 |
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1 |
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137-148 |
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Hylesia moths impact human health in South America, inducing epidemic outbreaks of lepidopterism, a puriginous dermatitis caused by the urticating properties of females' abdominal setae. The classification of the Hylesia genus is complex, owing to its high diversity in Amazonia, high intraspecific morphological variance, and lack of interspecific diagnostic traits which may hide cryptic species. Outbreaks of Hylesia metabus have been considered responsible for the intense outbreaks of lepidopterism in Venezuela and French Guiana since the C20, however, little is known about genetic variability throughout the species range, which is instrumental for establishing control strategies on H. metabus. Seven microsatellites and mitochondrial gene markers were analyzed from Hylesia moths collected from two major lepidopterism outbreak South American regions. The mitochondrial gene sequences contained significant genetic variation, revealing a single, widespread, polymorphic species with distinct clusters, possibly corresponding to populations evolving in isolation. The microsatellite markers validated the mitochondrial results, and suggest the presence of three populations: one in Venezuela, and two in French Guiana. All moths sampled during outbreak events in French Guiana were assigned to a single coastal population. The causes and implications of this finding require further research. |
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INRA, Unité de Recherche Ecologie des forêts méditerranéennes, Avignon, UR629, France |
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NLM (Medline) |
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19382928 (Issn) |
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Export Date: 1 February 2019 |
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EcoFoG @ webmaster @ |
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857 |
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Zinger, L.; Taberlet, P.; Schimann, H.; Bonin, A.; Boyer, F.; De Barba, M.; Gaucher, P.; Gielly, L.; Giguet-Covex, C.; Iribar, A.; Réjou-Méchain, M.; Rayé, G.; Rioux, D.; Schilling, V.; Tymen, B.; Viers, J.; Zouiten, C.; Thuiller, W.; Coissac, E.; Chave, J. |
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Title |
Body size determines soil community assembly in a tropical forest |
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Journal Article |
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Year |
2019 |
Publication |
Molecular Ecology |
Abbreviated Journal |
Mol Ecol |
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28 |
Issue |
3 |
Pages |
528-543 |
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DNA metabarcoding; eDNA; French Guiana; multitaxa; neutral assembly; niche determinism; propagule size; soil diversity |
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Tropical forests shelter an unparalleled biological diversity. The relative influence of environmental selection (i.e., abiotic conditions, biotic interactions) and stochastic?distance-dependent neutral processes (i.e., demography, dispersal) in shaping communities has been extensively studied for various organisms, but has rarely been explored across a large range of body sizes, in particular in soil environments. We built a detailed census of the whole soil biota in a 12-ha tropical forest plot using soil DNA metabarcoding. We show that the distribution of 19 taxonomic groups (ranging from microbes to mesofauna) is primarily stochastic, suggesting that neutral processes are prominent drivers of the assembly of these communities at this scale. We also identify aluminium, topography and plant species identity as weak, yet significant drivers of soil richness and community composition of bacteria, protists and to a lesser extent fungi. Finally, we show that body size, which determines the scale at which an organism perceives its environment, predicted the community assembly across taxonomic groups, with soil mesofauna assemblages being more stochastic than microbial ones. These results suggest that the relative contribution of neutral processes and environmental selection to community assembly directly depends on body size. Body size is hence an important determinant of community assembly rules at the scale of the ecological community in tropical soils and should be accounted for in spatial models of tropical soil food webs. |
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John Wiley & Sons, Ltd (10.1111) |
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0962-1083 |
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EcoFoG @ webmaster @ |
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873 |
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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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Year |
2019 |
Publication |
Nature |
Abbreviated Journal |
Nature |
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569 |
Issue |
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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EcoFoG @ webmaster @ |
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872 |
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Author |
Clair, B.; Ghislain, B.; Prunier, J.; Lehnebach, R.; Beauchene, J.; Alméras, T. |
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Title |
Mechanical contribution of secondary phloem to postural control in trees: the bark side of the force |
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Journal Article |
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Year |
2019 |
Publication |
New Phytologist |
Abbreviated Journal |
New Phytol |
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221 |
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1 |
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209-217 |
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Keywords |
bark; Malvaceae; maturation stress; secondary phloem; tree biomechanics |
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Summary To grow straight, plants need a motor system that controls posture by generating forces to offset gravity. This motor function in trees was long thought to be only controlled by internal forces induced in wood. Here we provide evidence that bark is involved in the generation of mechanical stresses in several tree species. Saplings of nine tropical species were grown tilted and staked in a shadehouse and the change in curvature of the stem was measured after releasing from the pole and after removing the bark. This first experiment evidenced the contribution of bark in the up-righting movement of tree stems. Combined mechanical measurements of released strains on adult trees and microstructural observations in both transverse and longitudinal/tangential plane enabled us to identify the mechanism responsible for the development of asymmetric mechanical stress in the bark of stems of these species. This mechanism does not result from cell wall maturation like in wood, or from the direct action of turgor pressure like in unlignified organs, but is the consequence of the interaction between wood radial pressure and a smartly organized trellis structure in the inner bark. |
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John Wiley & Sons, Ltd (10.1111) |
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0028-646x |
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doi: 10.1111/nph.15375 |
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EcoFoG @ webmaster @ |
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853 |
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Fichaux, M.; Béchade, B.; Donald, J.; Weyna, A.; Delabie, J.H.C.; Murienne, J.; Baraloto, C.; Orivel, J. |
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Title |
Habitats shape taxonomic and functional composition of Neotropical ant assemblages |
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Journal Article |
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2019 |
Publication |
Oecologia |
Abbreviated Journal |
Oecologia |
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189 |
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2 |
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501-513 |
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Formicidae; Functional diversity; Habitat filtering; Rainforest; Traits; Formicidae |
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Determining assembly rules of co-occurring species persists as a fundamental goal in community ecology. At local scales, the relative importance of environmental filtering vs. competitive exclusion remains a subject of debate. In this study, we assessed the relative importance of habitat filtering and competition in structuring understory ant communities in tropical forests of French Guiana. Leaf-litter ants were collected using pitfall and Winkler traps across swamp, slope and plateau forests near Saül, French Guiana. We used a combination of univariate and multivariate analyses to evaluate trait response of ants to habitat characteristics. Null model analyses were used to investigate the effects of habitat filtering and competitive interactions on community assembly at the scale of assemblages and sampling points, respectively. Swamp forests presented a much lower taxonomic and functional richness compared to slope and plateau forests. Furthermore, marked differences in taxonomic and functional composition were observed between swamp forests and slope or plateau forests. We found weak evidence for competitive exclusion based on null models. Nevertheless, the contrasting trait composition observed between habitats revealed differences in the ecological attributes of the species in the different forest habitats. Our analyses suggest that competitive interactions may not play an important role in structuring leaf-litter ant assemblages locally. Rather, habitats are responsible for driving both taxonomic and functional composition of ant communities. |
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International Center for Tropical Botany, Department of Biological Sciences, Florida International University, Miami, FL 33199, United States |
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Springer Verlag |
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00298549 (Issn) |
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EcoFoG @ webmaster @ |
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863 |
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Grossiord, C.; Christoffersen, B.; Alonso-Rodríguez, A.M.; Anderson-Teixeira, K.; Asbjornsen, H.; Aparecido, L.M.T.; Carter Berry, Z.; Baraloto, C.; Bonal, D.; Borrego, I.; Burban, B.; Chambers, J.Q.; Christianson, D.S.; Detto, M.; Faybishenko, B.; Fontes, C.G.; Fortunel, C.; Gimenez, B.O.; Jardine, K.J.; Kueppers, L.; Miller, G.R.; Moore, G.W.; Negron-Juarez, R.; Stahl, C.; Swenson, N.G.; Trotsiuk, V.; Varadharajan, C.; Warren, J.M.; Wolfe, B.T.; Wei, L.; Wood, T.E.; Xu, C.; McDowell, N.G. |
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Precipitation mediates sap flux sensitivity to evaporative demand in the neotropics |
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Journal Article |
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2019 |
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Oecologia |
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Oecologia |
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191 |
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3 |
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519-530 |
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Evapotranspiration; Plant functional traits; Transpiration; Vapor pressure deficit; drought; evapotranspiration; flux measurement; hydrological cycle; Neotropical Region; precipitation (chemistry); precipitation (climatology); tree; tropical forest; tropical region; vapor pressure; water; drought; evapotranspiration; forest; tree; vapor pressure; Droughts; Forests; Plant Transpiration; Trees; Vapor Pressure; Water |
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Transpiration in humid tropical forests modulates the global water cycle and is a key driver of climate regulation. Yet, our understanding of how tropical trees regulate sap flux in response to climate variability remains elusive. With a progressively warming climate, atmospheric evaporative demand [i.e., vapor pressure deficit (VPD)] will be increasingly important for plant functioning, becoming the major control of plant water use in the twenty-first century. Using measurements in 34 tree species at seven sites across a precipitation gradient in the neotropics, we determined how the maximum sap flux velocity (vmax) and the VPD threshold at which vmax is reached (VPDmax) vary with precipitation regime [mean annual precipitation (MAP); seasonal drought intensity (PDRY)] and two functional traits related to foliar and wood economics spectra [leaf mass per area (LMA); wood specific gravity (WSG)]. We show that, even though vmax is highly variable within sites, it follows a negative trend in response to increasing MAP and PDRY across sites. LMA and WSG exerted little effect on vmax and VPDmax, suggesting that these widely used functional traits provide limited explanatory power of dynamic plant responses to environmental variation within hyper-diverse forests. This study demonstrates that long-term precipitation plays an important role in the sap flux response of humid tropical forests to VPD. Our findings suggest that under higher evaporative demand, trees growing in wetter environments in humid tropical regions may be subjected to reduced water exchange with the atmosphere relative to trees growing in drier climates. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature. |
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Earth Systems Science Division, Pacific Northwest National Laboratory, Richland, WA, United States |
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Springer Verlag |
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00298549 (Issn) |
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EcoFoG @ webmaster @ |
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904 |
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