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Author Hartke, J.; Sprenger, P.P.; Sahm, J.; Winterberg, H.; Orivel, J.; Baur, H.; Beuerle, T.; Schmitt, T.; Feldmeyer, B.; Menzel, F. pdf  url
doi  openurl
  Title Cuticular hydrocarbons as potential mediators of cryptic species divergence in a mutualistic ant association Type Journal Article
  Year (down) 2019 Publication Ecology and Evolution Abbreviated Journal  
  Volume 9 Issue 16 Pages 9160-9176  
  Keywords environmental association; integrative taxonomy; niche differentiation; population structure; sexual selection; speciation  
  Abstract Upon advances in sequencing techniques, more and more morphologically identical organisms are identified as cryptic species. Often, mutualistic interactions are proposed as drivers of diversification. Species of the neotropical parabiotic ant association between Crematogaster levior and Camponotus femoratus are known for highly diverse cuticular hydrocarbon (CHC) profiles, which in insects serve as desiccation barrier but also as communication cues. In the present study, we investigated the association of the ants’ CHC profiles with genotypes and morphological traits, and discovered cryptic species pairs in both genera. To assess putative niche differentiation between the cryptic species, we conducted an environmental association study that included various climate variables, canopy cover, and mutualistic plant species. Although mostly sympatric, the two Camponotus species seem to prefer different climate niches. However in the two Crematogaster species, we could not detect any differences in niche preference. The strong differentiation in the CHC profiles may thus suggest a possible role during speciation itself either by inducing assortative mating or by reinforcing sexual selection after the speciation event. We did not detect any further niche differences in the environmental parameters tested. Thus, it remains open how the cryptic species avoid competitive exclusion, with scope for further investigations. © 2019 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.  
  Address Department of Evolutionary Animal Ecology, University of Bayreuth, Bayreuth, Germany  
  Corporate Author Thesis  
  Publisher John Wiley and Sons Ltd Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 20457758 (Issn) ISBN Medium  
  Area Expedition Conference  
  Notes Export Date: 2 September 2019; Correspondence Address: Hartke, J.; Senckenberg Biodiversity and Climate Research CentreGermany; email: Juliane.Hartke@senckenberg.de; Funding details: Leibniz-Gemeinschaft; Funding details: Agence Nationale de la Recherche, Not Available; Funding details: Deutsche Forschungsgemeinschaft, DFG, ME 3842/5‐1; Funding text 1: We thank Philippe Cerdan and Aurelie Dourdain for research permissions in the Hydreco Lab Petit Saut and the Paracou Research Station, respectively. Similarly, we thank Patrick Châtelet, Philippe Gaucher, and Dorothée Deslignes for permission to sample in the Les Nouragues Reserve. Further on, we thank Heike Stypa for supporting us in preparing the chemical samples. We thank Aidin Niamir for his helpful advice regarding climate data analysis. Financial support for this study was provided by the German Science Foundation (DFG) as a grant to Barbara Feldmeyer (FE 1333/7‐1), Thomas Schmitt (SCHM 2645/7‐1), and Florian Menzel (ME 3842/5‐1) and a grant managed by the French Agence Nationale de la Recherche (CEBA, ref. ANR‐10‐LABX‐25‐01) to Jérôme Orivel. The publication of this article was funded by the Open Access Fund of the Leibniz Association. Finally, we thank Markus Pfenninger and two anonymous reviewers for providing helpful comments on an earlier version of this manuscript.; References: Adler, P.B., HilleRisLambers, J., Levine, J.M., A niche for neutrality (2007) Ecology Letters, 10, pp. 95-104. , https://doi.org/10.1111/j.1461-0248.2006.00996.x; Aitchison, J., The statistical analysis of compositional data (1982) Journal of the Royal Statistical Society: Series B (Methodological), 44, pp. 139-177. , https://doi.org/10.1111/j.2517-6161.1982.tb01195.x; Andersson, M., Sexual selection, natural selection and quality advertisement (1982) Biological Journal of the Linnean Society, 17, pp. 375-393. , https://doi.org/10.1111/j.1095-8312.1982.tb02028.x; Bartlett, J.W., Frost, C., Reliability, repeatability and reproducibility: Analysis of measurement errors in continuous variables (2008) Ultrasound in Obstetrics and Gynecology, 31, pp. 466-475. , https://doi.org/10.1002/uog.5256; Baur, H., Kranz-Baltensperger, Y., Cruaud, A., Rasplus, J.Y., Timokhov, A.V., Gokhman, V.E., Morphometric analysis and taxonomic revision of Anisopteromalus Ruschka (Hymenoptera: Chalcidoidea: Pteromalidae) – An integrative approach (2014) Systematic Entomology, 39, pp. 691-709; Baur, H., Leuenberger, C., Analysis of ratios in multivariate morphometry (2011) Systematic Biology, 60, pp. 813-825. , https://doi.org/10.1093/sysbio/syr061; Bell, G., The distribution of abundance in neutral communities (2017) The American Naturalist, 155, p. 606. , https://doi.org/10.2307/3078983; Bickford, D., Lohman, D.J., Sodhi, N.S., Ng, P.K.L., Meier, R., Winker, K., Das, I., Cryptic species as a window on diversity and conservation (2007) Trends in Ecology & Evolution, 22, pp. 148-155. , https://doi.org/10.1016/j.tree.2006.11.004; Blomberg, S.P., Garland, T., Ives, A.R., Testing for phylogenetic signal in comparative data: Behavioral traits are more labile (2003) Evolution, 57, pp. 717-745; Blomquist, G.J., Structure and analysis of insect hydrocarbons (2010) Insect hydrocarbons: Biology, biochemistry, and chemical ecology, pp. 19-34. , G. J. Blomquist, A.-G. Bagnères, (Eds.),, New York, NY, Cambridge University Press; Blomquist, G.J., Bagnères, A.-G., Introduction: History and overview of insect hydrocarbons (2010) Insect hydrocarbons: Biology, biochemistry, and chemical ecology, pp. 3-18. , G. J. Blomquist, A.-G. Bagnères, (Eds.),, New York, NY, Cambridge University Press; Bolaños, L.M., Rosenblueth, M., Manrique de Lara, A., Migueles-Lozano, A., Gil-Aguillón, C., Mateo-Estrada, V., Martínez-Romero, E., Cophylogenetic analysis suggests cospeciation between the Scorpion Mycoplasma Clade symbionts and their hosts (2019) PLoS ONE, 14. , https://doi.org/10.1371/journal.pone.0209588; Bouckaert, R., Heled, J., Kühnert, D., Vaughan, T., Wu, C.-H., Xie, D., Drummond, A.J., BEAST 2: A Software Platform for Bayesian Evolutionary Analysis (2014) PLoS Computational Biology, 10. , https://doi.org/10.1371/journal.pcbi.1003537; Boyle, J.H., Martins, D., Musili, P.M., Pierce, N.E., Population genomics and demographic sampling of the ant-plant Vachellia drepanolobium and its symbiotic ants from sites across its range in East Africa (2018) Frontiers in Ecology and Evolution, 7, p. 206. , https://doi.org/10.3389/fevo.2019.00206; Brückner, A., Heethoff, M., A chemo-ecologists' practical guide to compositional data analysis (2017) Chemoecology, 27, pp. 33-46. , https://doi.org/10.1007/s00049-016-0227-8; Carlson, D.A., Bernier, U.R., Sutton, B.D., Elution patterns from capillary GC for methyl-branched alkanes (1998) Journal of Chemical Ecology, 24, pp. 1845-1865; Chomicki, G., Ward, P.S., Renner, S.S., Macroevolutionary assembly of ant/plant symbioses: Pseudomyrmex ants and their ant-housing plants in the Neotropics (2015) Proceedings of the Royal Society B: Biological Sciences, 282, p. 20152200; Chung, H., Carroll, S.B., Wax, sex and the origin of species: Dual roles of insect cuticular hydrocarbons in adaptation and mating (2015) BioEssays, 37, pp. 822-830. , https://doi.org/10.1002/bies.201500014; Chung, H., Loehlin, D.W., Dufour, H.D., Vaccaro, K., Millar, J.G., Carroll, S.B., A single gene affects both ecological divergence and mate choice in Drosophila (2014) Science, 343 (6175), pp. 1148-1151; Cruaud, A., Rønsted, N., Chantarasuwan, B., Chou, L.S., Clement, W.L., Couloux, A., Savolainen, V., An extreme case of plant – insect codiversification: Figs and fig-pollinating wasps (2012) Systematic Biology, 61, pp. 1029-1047. , https://doi.org/10.1093/sysbio/sys068; Csösz, S., Wagner, H.C., Bozsó, M., Seifert, B., Arthofer, W., Schlick-Steiner, B.C., Pénzes, Z., Tetramorium indocile Santschi, 1927 stat. rev. is the proposed scientific name for Tetramorium sp. C sensu Schlick-Steiner et al. (2006) based on combined molecular and morphological evidence (Hymenoptera: Formicidae) (2014) Zoologischer Anzeiger, 253, pp. 469-481; Darwell, C.T., Cook, J.M., Cryptic diversity in a fig wasp community — morphologically differentiated species are sympatric but cryptic species are parapatric (2017) Molecular Ecology, 26, pp. 937-950. , https://doi.org/10.1111/mec.13985; Davidson, D.W., Ecological studies of Neotropical ant gardens (1988) Ecology, 69, pp. 1138-1152. , https://doi.org/10.2307/1941268; De Queiroz, K., Species concepts and species delimitation (2007) Systematic Biology, 56, pp. 879-886. , https://doi.org/10.1080/10635150701701083; de Vienne, D.M., Refrégier, G., López-Villavicencio, M., Tellier, A., Hood, M.E., Giraud, T., Cospeciation vs host-shift speciation: Methods for testing, evidence from natural associations and relation to coevolution (2013) New Phytologist, 198, pp. 347-385. , https://doi.org/10.1111/nph.12150; Degnan, P.H., Lazarus, A.B., Brock, C.D., Wernegreen, J.J., Host – symbiont stability and fast evolutionary rates in an ant – Bacterium Association: Cospeciation of Camponotus species and their endosymbionts, Candidatus Blochmannia (2004) Systematic Biology, 53, pp. 95-110. , https://doi.org/10.1080/10635150490264842; Dieckmann, U., Doebeli, M., On the origin of species by sympatric speciation (1999) Nature, 400, pp. 354-357. , https://doi.org/10.1038/22521; Doebeli, M., Dieckmann, U., Evolutionary branching and sympatric speciation caused by different types of ecological interactions (2000) The American Naturalist, 156, pp. S77-S101. , https://doi.org/10.1086/303417; Emery, V.J., Tsutsui, N.D., Recognition in a social symbiosis: Chemical phenotypes and nestmate recognition behaviors of Neotropical parabiotic ants (2013) PLoS ONE, 8. , https://doi.org/10.1371/journal.pone.0056492; Excoffier, L., Lischer, H.E.L., Arlequin suite ver 3.5: A new series of programs to perform population genetics analyses under Linux and Windows (2010) Molecular Ecology Resources, 10, pp. 564-567; García-Robledo, C., Kuprewicz, E.K., Staines, C.L., Erwin, T.L., Kress, W.J., Limited tolerance by insects to high temperatures across tropical elevational gradients and the implications of global warming for extinction (2015) Proceedings of the National Academy of Sciences of the United States of America, 113, pp. 680-685. , https://doi.org/10.1073/pnas.1507681113; Gause, G.F., Experimental studies on the struggle for existence I. Mixed population of two species of yeast (1932) Journal of Experimental Biology, 9, pp. 389-402; Gebiola, M., Monti, M.M., Johnson, R.C., Woolley, J.B., Hunter, M.S., Giorgini, M., Pedata, P.A., A revision of the Encarsia pergandiella species complex (Hymenoptera: Aphelinidae) shows cryptic diversity in parasitoids of whitefly pests (2017) Systematic Entomology, 42, pp. 31-59; Grundt, H.H., Kjølner, S., Borgen, L., Rieseberg, L.H., Brochmann, C., High biological species diversity in the arctic flora (2006) Proceedings of the National Academy of Sciences of the United States of America, 103, pp. 972-975. , https://doi.org/10.1073/pnas.0510270103; Guimarães, P.R., Jordano, P., Thompson, J.N., Evolution and coevolution in mutualistic networks (2011) Ecology Letters, 14, pp. 877-885. , https://doi.org/10.1111/j.1461-0248.2011.01649.x; Gustafson, K.D., Kensinger, B.J., Bolek, M.G., Luttbeg, B., Distinct snail (Physa) morphotypes from different habitats converge in shell shape and size under common garden conditions (2014) Evolutionary Ecology Research, 16, pp. 77-89; Han, M.V., Zmasek, C.M., PhyloXML: XML for evolutionary biology and comparative genomics (2009) BMC Bioinformatics, 10, p. 356. , https://doi.org/10.1186/1471-2105-10-356; Hardin, G., The competitive exclusion principle (1960) Science, 131, pp. 1292-1297; Heethoff, M., Laumann, M., Weigmann, G., Raspotnig, G., Integrative taxonomy: Combining chemical, morphological and molecular data for delineation of the parthenogenetic Trhypochthonius tectorum complex (Acari, Oribatida, Trhypochthoniidae) (2011) Frontiers in Zoology, 8, p. 2; Hoeksema, J.D., Bruna, E.M., Pursuing the big questions about interspecific mutualism: A review of theoretical approaches (2000) Oecologia, 125, pp. 321-330. , https://doi.org/10.1007/s004420000496; Hoffmann, A.A., Turelli, M., Simmons, G.M., Unidirectional incompatibility between populations of Drosophila simulans (1986) Evolution, 40, pp. 692-701; Hosokawa, T., Kikuchi, Y., Nikoh, N., Shimada, M., Fukatsu, T., Strict Host-Symbiont cospeciation and reductive genome evolution in insect gut bacteria (2006) PLoS Biology, 4. , https://doi.org/10.1371/journal.pbio.0040337; Hubbell, S.P., (2001) The unified neutral theory of biodiversity and biogeography, , Princeton, NJ, Princeton University Press; Hubbell, S.P., Neutral theory in community ecology and the hypothesis of functional equivalence (2005) Functional Ecology, 19, pp. 166-172. , https://doi.org/10.1111/j.0269-8463.2005.00965.x; Hudson, E.J., Price, T.D., Pervasive reinforcement and the role of sexual selection in biological speciation (2014) Journal of Heredity, 105, pp. 821-833. , https://doi.org/10.1093/jhered/esu041; Janz, N., Nyblom, K., Nylin, S., Evolutionary dynamics of host-plant specialization: A case study of the Tribe Nymohalini (2001) Evolution, 55, pp. 783-796; Jousselin, E., van Noort, S., Berry, V., Rasplus, J.-Y., Rønsted, N., Erasmus, J.C., Greeff, J.M., One fig to bind them all: Host conservatism in a fig wasp community unraveled by cospeciation analyses among pollinating and nonpollinating fig wasps (2008) Evolution, 62, pp. 1777-1797. , https://doi.org/10.1111/j.1558-5646.2008.00406.x; Kamilar, J.M., Cooper, N., Phylogenetic singal in primate behaviour, ecolog anf life history (2013) Philosophical Transactions of the Royal Society of London. Series B, 368, p. 20120341; Karger, D.N., Conrad, O., Böhner, J., Kawohl, T., Kreft, H., Soria-Auza, R.W., Kessler, M., Climatologies at high resolution for the earth's land surface areas (2017) Scientific Data, 4, p. 170122. , https://doi.org/10.1038/sdata.2017.122; Kawakita, A., Takimura, A., Terachi, T., Sota, T., Kato, M., Cospeciation analysis of an obligate pollination mutualism: Have Glochidon trees (Euphorbiaceae) and pollinating Epicephala moths (Gracillaridae) diverified in parallel? (2004) Evolution, 58, pp. 2201-2214; Klingenberg, C.P., Size, shape, and form: Concepts of allometry in geometric morphometrics (2016) Development Genes and Evolution, 226, pp. 113-137. , https://doi.org/10.1007/s00427-016-0539-2; Kumar, S., Stecher, G., Li, M., Knyaz, C., Tamura, K., MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms (2018) Molecular Biology and Evolution, 35, pp. 1547-1549. , https://doi.org/10.1093/molbev/msy096; Leavitt, D.H., Starrett, J., Westphal, M.F., Hedin, M., Multilocus sequence data reveal dozens of putative cryptic species in a radiation of endemic Californian mygalomorph spiders (Araneae, Mygalomorphae, Nemesiidae) (2015) Molecular Phylogenetics and Evolution, 91, pp. 56-67. , https://doi.org/10.1016/j.ympev.2015.05.016; Leigh, J.W., Bryant, D., POPART: Full-feature software for haplotype network construction (2015) Methods in Ecology and Evolution, 6, pp. 1110-1116; Liaw, A., Wiener, M., Classification and regression by randomForest (2002) R News, 2, pp. 18-22; Martin, S.J., Helanterä, H., Drijfhout, F.P., Evolution of species-specific cuticular hydrocarbon patterns in Formica ants (2008) Biological Journal of the Linnean Society, 95, pp. 131-140. , https://doi.org/10.1111/j.1095-8312.2008.01038.x; Menzel, F., Blaimer, B.B., Schmitt, T., How do cuticular hydrocarbons evolve? Physiological constraints and climatic and biotic selection pressures act on a complex functional trait (2017) Proceedings of the Royal Society B-Biological Sciences, 284, p. 20161727. , https://doi.org/10.1098/rspb.2016.1727; Menzel, F., Linsenmair, K.E., Blüthgen, N., Selective interspecific tolerance in tropical Crematogaster-Camponotus associations (2008) Animal Behavior, 75, pp. 837-846. , https://doi.org/10.1016/j.anbehav.2007.07.005; Menzel, F., Orivel, J., Kaltenpoth, M., Schmitt, T., What makes you a potential partner? Insights from convergently evolved ant-ant symbioses (2014) Chemoecology, 24, pp. 105-119. , https://doi.org/10.1007/s00049-014-0149-2; Menzel, F., Schmitt, T., Blaimer, B.B., The evolution of a complex trait: Cuticular hydrocarbons in ants evolve independent from phylogenetic constraints (2017) Journal of Evolutionary Biology, 30, pp. 1372-1385. , https://doi.org/10.1111/jeb.13115; Montero-Pau, J., Gomez, A., Muñoz, J., Application of an inexpensive and high-throughput genomic DNA extraction method for the molecular ecology of zooplanktonic diapausing eggs (2008) Limnology and Oceanography: Methods, 6, pp. 218-222. , https://doi.org/10.4319/lom.2008.6.218; Nosil, P., (2012) Ecological speciation, , Oxford, UK, Oxford University Press; Oksanen, J., Blanchet, F.G., Friendly, M., Kindt, R., Legendre, P., McGlinn, D., Wagner, H., (2016) vegan: Community Ecology Package, , https://cran.r-project.org/web/packages/vegan/; Orivel, J., Errard, C., Dejean, A., Ant gardens: Interspecific recognition in parabiotic ant species (1997) Behavioral Ecology and Sociobiology, 40, pp. 87-93. , https://doi.org/10.1007/s002650050319; Paradis, E., Pegas: An R package for population genetics with an integrated-modular approach (2010) Bioinformatics, 26, pp. 419-420. , https://doi.org/10.1093/bioinformatics/btp696; Quek, S.-P., Davies, S.J., Itino, T., Pierce, N.E., Codiversification in an ant-plant mutualism: Stem texture and the evolution of host use in Crematogaster (Formicidae: Myrmicinae) Inhabitants of Macaranga (Euphorbiaceae) (2004) Evolution, 58, pp. 554-570; (2018) R: A language and environment for statistical computing, , Vienna, Austria, R Foundation for Statistical Computing; Rambaut, A., Drummond, A.J., Xie, D., Baele, G., Suchard, M.A., Posterior summarization in Bayesian Phylogenetics using Tracer 1.7 (2018) Systematic Biology, 67, pp. 901-904. , https://doi.org/10.1093/sysbio/syy032; Ronquist, F., Teslenko, M., Van Der Mark, P., Ayres, D.L., Darling, A., Höhna, S., Huelsenbeck, J.P., MrBayes 3.2: Efficient bayesian phylogenetic inference and model choice across a large model space (2012) Systematic Biology, 61, pp. 539-542; Schlenke, T.A., Begun, D.J., Strong selective sweep associated with a transposon insertion in Drosophila simulans (2004) Proceedings of the National Academy of Sciences of the United States of America, 101, pp. 1626-1631. , https://doi.org/10.1073/pnas.0303793101; Schuler, H., Köppler, K., Daxböck-Horvath, S., Rasool, B., Krumböck, S., Schwarz, D., Riegler, M., The hitchhiker's guide to Europe: The infection dynamics of an ongoing Wolbachia invasion and mitochondrial selective sweep in Rhagoletis cerasi (2016) Molecular Ecology, 25, pp. 1595-1609; Schultz, T.R., Solomon, S.A., Mueller, U.G., Villesen, P., Boomsma, J.J., Adams, R.M.M., Norden, B., Cryptic speciation in the fungus-growing ants Cyphomyrmex longiscapus Weber and Cyphomyrmex muelleri Schultz and Solomon, new species (Formicidae, Attini) (2002) Insectes Sociaux, 49, pp. 331-343. , https://doi.org/10.1007/PL00012657; Schwander, T., Arbuthnott, D., Gries, R., Gries, G., Nosil, P., Crespi, B.J., Hydrocarbon divergence and reproductive isolation in Timema stick insects (2013) BMC Evolutionary Biology, 13, p. 151. , https://doi.org/10.1186/1471-2148-13-151; Scriven, J.J., Whitehorn, P.R., Goulson, D., Tinsley, M.C., Niche partitioning in a sympatric cryptic species complex (2016) Ecology and Evolution, 6, pp. 1328-1339. , https://doi.org/10.1002/ece3.1965; Seifert, B., Removal of allometric variance improves species separation in multi-character discriminant functions when species are strongly allometric and exposes diagnostic characters (2008) Myrmecological News, 11, pp. 91-105; Servedio, M.R., Van Doorn, G.S., Kopp, M., Frame, A.M., Nosil, P., Magic traits in speciation: “magic” but not rare? (2011) Trends in Ecology & Evolution, 26, pp. 389-397; Smadja, C., Butlin, R.K., On the scent of speciation: The chemosensory system and its role in premating isolation (2009) Heredity, 102, pp. 77-97. , https://doi.org/10.1038/hdy.2008.55; Steiner, F.M., Csöcs, S., Markó, B., Gamisch, A., Rinnhofer, L., Folterbauer, C., Schlick-Steiner, B.C., Molecular phylogenetics and evolution turning one into five: Integrative taxonomy uncovers complex evolution of cryptic species in the harvester ant Messor “structor” (2018) Molecular Phylogenetics and Evolution, 127, pp. 387-404. , https://doi.org/10.1016/j.ympev.2018.04.005; Stork, N.E., How many species of insects and other terrestrial arthropods are there on earth? (2018) Annual Review of Ecology Evolution and Systematics, 63, pp. 31-45; Ströher, P.R., Li, C., Pie, M.R., Exon-primed intron-crossing (EPIC) markers as a tool for ant phylogeography (2013) Revista Brasileira de Entomologia, 57, pp. 427-430. , https://doi.org/10.1590/S0085-56262013005000039; Struck, T.H., Feder, J.L., Bendiksby, M., Birkeland, S., Cerca, J., Gusarov, V.I., Dimitrov, D., Finding evolutionary processes hidden in cryptic species (2018) Trends in Ecology & Evolution, 33, pp. 153-163. , https://doi.org/10.1016/j.tree.2017.11.007; Tajima, F., Statistical method for testing the neutral mutation hypothesis by DNA polymorphism (1989) Genetics, 123, pp. 585-595; Tamura, K., Nei, M., Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees (1993) Molecular Biology and Evolution, 10, pp. 512-526; Thibert-Plante, X., Gavrilets, S., Evolution of mate choice and the so-called magic traits in ecological speciation (2013) Ecology Letters, 16, pp. 1004-1013. , https://doi.org/10.1111/ele.12131; Thomas, M.L., Simmons, L.W., Sexual dimorphism in cuticular hydrocarbons of the Australian field cricket Teleogryllus oceanicus (Orthoptera: Gryllidae) (2008) Journal of Insect Physiology, 54, pp. 1081-1089. , https://doi.org/10.1016/j.jinsphys.2008.04.012; Thompson, J.D., Higgins, D.G., Gibson, T.J., CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice (1994) Nucleic Acids Research, 22, pp. 4673-4680. , https://doi.org/10.1093/nar/22.22.4673; Thompson, J.N., Schwind, C., Guimarães, P.R., Friberg, M., Diversification through multitrait evolution in a coevolving interaction (2013) Proceedings of the National Academy of Sciences of the United States of America, 110, pp. 11487-11492. , https://doi.org/10.1073/pnas.1307451110; Türke, M., Fiala, B., Linsenmair, K.E., Feldhaar, H., Estimation of dispersal distances of the obligately plant-associated ant Crematogaster decamera (2010) Ecological Entomology, 35, pp. 662-671. , https://doi.org/10.1111/j.1365-2311.2010.01222.x; van Wilgenburg, E., Symonds, M.R.E., Elgar, M.A., Evolution of cuticular hydrocarbon diversity in ants (2011) Journal of Evolutionary Biology, 24, pp. 1188-1198. , https://doi.org/10.1111/j.1420-9101.2011.02248.x; van Zweden, J.S., d'Ettorre, P., Nestmate recognition in social insects and the role of hydrocarbons (2010) Insect hydrocarbons: Biology, biochemistry, and chemical ecology, pp. 222-243. , G. J. Blomquist, A.-G. Bagnères, (Eds.),, New York, NY, Cambridge University Press; Vantaux, A., Dejean, A., Dor, A., Orivel, J., Parasitism versus mutualism in the ant-garden parabiosis between Camponotus femoratus and Crematogaster levior (2007) Insectes Sociaux, 54, pp. 95-99. , https://doi.org/10.1007/s00040-007-0914-0; Violle, C., Nemergut, D.R., Pu, Z., Jiang, L., Phylogenetic limiting similarity and competitive exclusion (2011) Ecology Letters, 14, pp. 782-787. , https://doi.org/10.1111/j.1461-0248.2011.01644.x; Vodă, R., Dapporto, L., Dincă, V., Vila, R., Why do cryptic species tend not to co-occur? A case study on two cryptic pairs of butterflies (2015) PLoS ONE, 10. , https://doi.org/10.1371/journal.pone.0117802; Wickham, H., (2016) ggplot2: Elegant graphics for data analysis, , 2nd ed., New York, NY, Springer-Verlag; Wolak, M.E., Fairbairn, D.J., Paulsen, Y.R., Guidelines for estimating repeatability (2012) Methods in Ecology and Evolution, 3, pp. 129-137. , https://doi.org/10.1111/j.2041-210X.2011.00125.x Approved no  
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Author Ruiz-González, M.X.; Leroy, C.; Dejean, A.; Gryta, H.; Jargeat, P.; Carrión, A.D.A.; Orivel, J. pdf  url
doi  openurl
  Title Do host plant and associated ant species affect microbial communities in myrmecophytes? Type Journal Article
  Year (down) 2019 Publication Insects Abbreviated Journal Insects  
  Volume 10 Issue 11 Pages 391  
  Keywords Allomerus decemarticulatus; Allomerus octoarticulatus; Azteca sp; Cf; Cordia nodosa; Depilis; Domatia; Hirtella physophora; Microbial diversity  
  Abstract 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.  
  Address Biodiversity Genomics Team, Plant Ecophysiology & Evolution Group, Guangxi Key Laboratory of Forest Ecology and Conservation, College of Forestry, Daxuedonglu 100, Nanning, Guangxi 530005, China  
  Corporate Author Thesis  
  Publisher Mdpi Ag Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 20754450 (Issn) ISBN Medium  
  Area Expedition Conference  
  Notes 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 Approved no  
  Call Number EcoFoG @ webmaster @ Serial 896  
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Author Ghislain, B.; Engel, J.; Clair, B.; Donaldson, L.; Baas, P. url  doi
openurl 
  Title Diversity of anatomical structure of tension wood among 242 tropical tree species Type Journal Article
  Year (down) 2019 Publication IAWA Journal Abbreviated Journal  
  Volume 40 Issue 4 Pages 765-784  
  Keywords  
  Abstract Angiosperm trees produce tension wood to actively control their vertical position. Tension wood has often been characterised by the presence of an unlignified inner fibre wall layer called the G-layer. Using this definition, previous reports indicate that only one-third of all tree species have tension wood with G-layers. Here we aim to (i) describe the large diversity of tension wood anatomy in tropical tree species, taking advantage of the recent understanding of tension wood anatomy and (ii) explore any link between this diversity and other ecological traits of the species. We sampled tension wood and normal wood in 432 trees from 242 species in French Guiana. The samples were observed using safranin and astra blue staining combined with optical microscopy. Species were assigned to four anatomical groups depending on the presence/absence of G-layers, and their degree of lignification. The groups were analysed for functional traits including wood density and light preferences. Eighty-six% of the species had G-layers in their tension wood which was lignified in most species, with various patterns of lignification. Only a few species did not have G-layers. We found significantly more species with lignified G-layers among shade-tolerant and shade-demanding species as well as species with a high wood density. Our results bring up-to-date the incidence of species with/without G-layers in the tropical lowland forest where lignified G-layers are the most common anatomy of tension wood. Species without G-layers may share a common mechanism with the bark motor taking over the wood motor. We discuss the functional role of lignin in the G-layer.  
  Address  
  Corporate Author Thesis  
  Publisher Brill Place of Publication Leiden, The Netherlands Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number EcoFoG @ webmaster @ Serial 903  
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Author Bréchet, L.; Courtois, E.A.; Saint-Germain, T.; Janssens, I.A.; Asensio, D.; Ramirez-Rojas, I.; Soong, J.L.; Van Langenhove, L.; Verbruggen, E.; Stahl, C. pdf  url
doi  openurl
  Title Disentangling Drought and Nutrient Effects on Soil Carbon Dioxide and Methane Fluxes in a Tropical Forest Type Journal Article
  Year (down) 2019 Publication Frontiers in Environmental Science Abbreviated Journal Front. Environ. Sci.  
  Volume 7 Issue 180 Pages  
  Keywords carbon dioxide; drought; fertilization; methane; nitrogen; phosphorus; soil GHG fluxes; tropical forest  
  Abstract Tropical soils are a major contributor to the balance of greenhouse gas (GHG) fluxes in the atmosphere. Models of tropical GHG fluxes predict that both the frequency of drought events and changes in atmospheric deposition of nitrogen (N) will significantly affect dynamics of soil carbon dioxide (CO2) and methane (CH4) production and consumption. In this study, we examined the combined effect of a reduction in precipitation and an increase in nutrient availability on soil CO2 and CH4 fluxes in a primary French Guiana tropical forest. Drought conditions were simulated by intercepting precipitation falling through the forest canopy with tarpaulin roofs. Nutrient availability was manipulated through application of granular N and/or phosphorus (P) fertilizer to the soil. Soil water content (SWC) below the roofs decreased rapidly and stayed at continuously low values until roof removal, which as a consequence roughly doubled the duration of the dry season. After roof removal, SWC slowly increased but remained lower than in the control soils even after 2.5 months of wet-season precipitation. We showed that drought-imposed reduction in SWC decreased the CO2 emissions (i.e., CO2 efflux), but strongly increased the CH4 emissions. N, P, and N × P (i.e., NP) additions all significantly increased CO2 emission but had no effect on CH4 fluxes. In treatments where both fertilization and drought were applied, the positive effect of N, P, and NP fertilization on CO2 efflux was reduced. After roof removal, soil CO2 efflux was more resilient in the control plots than in the fertilized plots while there was only a modest effect of roof removal on soil CH4 fluxes. Our results suggest that a combined increase in drought and nutrient availability in soil can locally increase the emissions of both CO2 and CH4 from tropical soils, for a long term.  
  Address Lawrence Berkeley National Laboratory, Climate and Ecosystem Science Division, Berkeley, CA, United States  
  Corporate Author Thesis  
  Publisher Frontiers Media S.A. Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 2296665x (Issn) ISBN Medium  
  Area Expedition Conference  
  Notes Export Date: 16 December 2019; Correspondence Address: Bréchet, L.; Centre of Excellence PLECO (Plant and Ecosystems), Department of Biology, University of AntwerpBelgium; email: laeti.brechet@gmail.com Approved no  
  Call Number EcoFoG @ webmaster @ Serial 899  
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Author Ghislain, B.; Alméras, T.; Prunier, J.; Clair, B. pdf  url
doi  openurl
  Title Contributions of bark and tension wood and role of the G-layer lignification in the gravitropic movements of 21 tropical tree species Type Journal Article
  Year (down) 2019 Publication Annals of Forest Science Abbreviated Journal Ann. Forest Sci.  
  Volume 76 Issue 4 Pages 107  
  Keywords Bark; Biomechanics; G-layer; Lignification; Tension wood; Tropical rainforest; Magnoliophyta  
  Abstract Key message: Gravitropic movements in angiosperm woody stems are achieved through the action of bark and/or wood motor, depending on the bark and wood fibre anatomy (with trellis structure or not; with G-layers or not). Bark motor is as efficient as wood motor to recover from tilting in young trees of 21 tropical species. Context: Angiosperm trees produce tension wood to control their orientation through changes in stem curvature. Tension wood is classified into 3 anatomical groups: with unlignified G-layer, with lignified G-layer and without G-layer. Aims: This study aimed at assessing whether this anatomical diversity reflects a diversity in efficiency of gravitropic movement. Methods: The study was conducted on tropical seedling from the three anatomical groups. Seedlings were staked and grown tilted. At the end of the experiment, changes in curvature when releasing the stem from the stake and when removing bark were measured. Three parameters were computed to compare the global efficiency of gravitropism (stem gravitropic efficiency) and the specific efficiency of motor mechanism based on wood (maturation strain of tension wood) and bark (standardized debarking curvature). Results: The maturation strain of tension wood was similar between species with unlignified and lignified G-layer. Species without G-layer exhibited low maturation strain and large debarking curvature, showing they rely on bark for gravitropism. Bark and wood achieved similar motor efficiency. Conclusion: Lignin does not affect the generation of tensile stress in the G-layer. Bark can be as efficient as wood as a motor of gravitropic movements. © 2019, The Author(s).  
  Address Laboratoire de Mécanique et Génie Civil (LMGC), Université de Montpellier, CNRS, Montpellier, 34095, France  
  Corporate Author Thesis  
  Publisher Springer Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 12864560 (Issn) ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number EcoFoG @ webmaster @ Serial 900  
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Author Ziegler, C.; Coste, S.; Stahl, C.; Delzon, S.; Levionnois, S.; Cazal, J.; Cochard, H.; Esquivel-Muelbert, A.; Goret, J.-Y.; Heuret, P.; Jaouen, G.; Santiago, L.S.; Bonal, D. url  doi
openurl 
  Title Large hydraulic safety margins protect Neotropical canopy rainforest tree species against hydraulic failure during drought Type Journal Article
  Year (down) 2019 Publication Annals of Forest Science Abbreviated Journal Ann. Forest Sci.  
  Volume 76 Issue 4 Pages 115  
  Keywords Amazon rainforest; Embolism resistance; Hydraulic safety margins; Turgor loss point; Water potential  
  Abstract Key message: Abundant Neotropical canopy-tree species are more resistant to drought-induced branch embolism than what is currently admitted. Large hydraulic safety margins protect them from hydraulic failure under actual drought conditions. Context: Xylem vulnerability to embolism, which is associated to survival under extreme drought conditions, is being increasingly studied in the tropics, but data on the risk of hydraulic failure for lowland Neotropical rainforest canopy-tree species, thought to be highly vulnerable, are lacking. Aims: The purpose of this study was to gain more knowledge on species drought-resistance characteristics in branches and leaves and the risk of hydraulic failure of abundant rainforest canopy-tree species during the dry season. Methods: We first assessed the range of branch xylem vulnerability to embolism using the flow-centrifuge technique on 1-m-long sun-exposed branches and evaluated hydraulic safety margins with leaf turgor loss point and midday water potential during normal- and severe-intensity dry seasons for a large set of Amazonian rainforest canopy-tree species. Results: Tree species exhibited a broad range of embolism resistance, with the pressure threshold inducing 50% loss of branch hydraulic conductivity varying from − 1.86 to − 7.63 MPa. Conversely, we found low variability in leaf turgor loss point and dry season midday leaf water potential, and mostly large, positive hydraulic safety margins. Conclusions: Rainforest canopy-tree species growing under elevated mean annual precipitation can have high resistance to embolism and are more resistant than what was previously thought. Thanks to early leaf turgor loss and high embolism resistance, most species have a low risk of hydraulic failure and are well able to withstand normal and even severe dry seasons. © 2019, The Author(s).  
  Address Smithsonian Tropical Research Institute, Balboa, Ancon, Panama  
  Corporate Author Thesis  
  Publisher Springer Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 12864560 (Issn) ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number EcoFoG @ webmaster @ Serial 901  
Permanent link to this record
 

 
Author Barassé, V.; Touchard, A.; Téné, N.; Tindo, M.; Kenne, M.; Klopp, C.; Dejean, A.; Bonnafé, E.; Treilhou, M. pdf  url
doi  openurl
  Title The peptide venom composition of the fierce stinging ant tetraponera aethiops (formicidae: Pseudomyrmecinae) Type Journal Article
  Year (down) 2019 Publication Toxins Abbreviated Journal Toxins  
  Volume 11 Issue 12 Pages 732  
  Keywords Defensive venom; Dimeric peptides; Peptidome; Tetraponera aethiops  
  Abstract In the mutualisms involving certain pseudomyrmicine ants and different myrmecophytes (i.e., plants sheltering colonies of specialized “plant-ant” species in hollow structures), the ant venom contributes to the host plant biotic defenses by inducing the rapid paralysis of defoliating insects and causing intense pain to browsing mammals. Using integrated transcriptomic and proteomic approaches, we identified the venom peptidome of the plant-ant Tetraponera aethiops (Pseudomyrmecinae). The transcriptomic analysis of its venom glands revealed that 40% of the expressed contigs encoded only seven peptide precursors related to the ant venom peptides from the A-superfamily. Among the 12 peptide masses detected by liquid chromatography-mass spectrometry (LC-MS), nine mature peptide sequences were characterized and confirmed through proteomic analysis. These venom peptides, called pseudomyrmecitoxins (PSDTX), share amino acid sequence identities with myrmeciitoxins known for their dual offensive and defensive functions on both insects and mammals. Furthermore, we demonstrated through reduction/alkylation of the crude venom that four PSDTXs were homo- and heterodimeric. Thus, we provide the first insights into the defensive venom composition of the ant genus Tetraponera indicative of a streamlined peptidome.  
  Address CNRS, UMR EcoFoG, AgroParisTech, Cirad, INRA, Université des Antilles, Université de Guyane, Kourou, 97310, France  
  Corporate Author Thesis  
  Publisher Mdpi Ag Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 20726651 (Issn) ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number EcoFoG @ webmaster @ Serial 902  
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Author 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. url  doi
openurl 
  Title Precipitation mediates sap flux sensitivity to evaporative demand in the neotropics Type Journal Article
  Year (down) 2019 Publication Oecologia Abbreviated Journal Oecologia  
  Volume 191 Issue 3 Pages 519-530  
  Keywords 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  
  Abstract 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.  
  Address Earth Systems Science Division, Pacific Northwest National Laboratory, Richland, WA, United States  
  Corporate Author Thesis  
  Publisher Springer Verlag Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 00298549 (Issn) ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number EcoFoG @ webmaster @ Serial 904  
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Author Honorio Coronado, E.N.; Blanc-Jolivet, C.; Mader, M.; García-Dávila, C.R.; Sebbenn, A.M.; Meyer-Sand, B.R.V.; Paredes-Villanueva, K.; Tysklind, N.; Troispoux, V.; Massot, M.; Degen, B. url  doi
openurl 
  Title Development of nuclear and plastid SNP markers for genetic studies of Dipteryx tree species in Amazonia Type Journal Article
  Year (down) 2019 Publication Conservation Genetics Resources Abbreviated Journal Conserv. Genet. Res.  
  Volume 11 Issue 3 Pages 333-336  
  Keywords  
  Abstract We developed nuclear and plastid single nucleotide polymorphism (SNP) and insertion/deletion (INDEL) markers for Dipteryx species using a combination of restriction associated DNA sequencing (RADSeq) and low coverage MiSeq genome sequencing. Of the total 315 loci genotyped using a MassARRAY platform, 292 loci were variable and polymorphic among the 73 sampled individuals from French Guiana, Brasil, Peru, and Bolivia. A final set of 56 nuclear SNPs, 26 chloroplast SNPs, 2 chloroplast INDELs, and 32 mitochondrial SNPs identifying significant population structure was developed. This set of loci will be useful for studies on population genetics of Dipteryx species in Amazonia.  
  Address  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1877-7260 ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number EcoFoG @ webmaster @ Honorio Coronado2019 Serial 906  
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Author 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. pdf  url
doi  openurl
  Title Compositional response of Amazon forests to climate change Type Journal Article
  Year (down) 2019 Publication Global Change Biology Abbreviated Journal Global Change Biol.  
  Volume 25 Issue 1 Pages 39-56  
  Keywords 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  
  Abstract 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.  
  Address Museu Paraense Emílio Goeldi, Pará, Brazil  
  Corporate Author Thesis  
  Publisher Blackwell Publishing Ltd Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 13541013 (Issn) ISBN Medium  
  Area Expedition Conference  
  Notes 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 Approved no  
  Call Number EcoFoG @ webmaster @ Serial 905  
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