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Author Hudson, L.N.; Newbold, T.; Contu, S.; Hill, S.L.L.; Lysenko, I.; De Palma, A.; Phillips, H.R.P.; Alhusseini, T.I.; Bedford, F.E.; Bennett, D.J.; Booth, H.; Burton, V.J.; Chng, C.W.T.; Choimes, A.; Correia, D.L.P.; Day, J.; Echeverría-Londoño, S.; Emerson, S.R.; Gao, D.; Garon, M.; Harrison, M.L.K.; Ingram, D.J.; Jung, M.; Kemp, V.; Kirkpatrick, L.; Martin, C.D.; Pan, Y.; Pask-Hale, G.D.; Pynegar, E.L.; Robinson, A.N.; Sanchez-Ortiz, K.; Senior, R.A.; Simmons, B.I.; White, H.J.; Zhang, H.; Aben, J.; Abrahamczyk, S.; Adum, G.B.; Aguilar-Barquero, V.; Aizen, M.A.; Albertos, B.; Alcala, E.L.; del Mar Alguacil, M.; Alignier, A.; Ancrenaz, M.; Andersen, A.N.; Arbeláez-Cortés, E.; Armbrecht, I.; Arroyo-Rodríguez, V.; Aumann, T.; Axmacher, J.C.; Azhar, B.; Azpiroz, A.B.; Baeten, L.; Bakayoko, A.; Báldi, A.; Banks, J.E.; Baral, S.K.; Barlow, J.; Barratt, B.I.P.; Barrico, L.; Bartolommei, P.; Barton, D.M.; Basset, Y.; Batáry, P.; Bates, A.J.; Baur, B.; Bayne, E.M.; Beja, P.; Benedick, S.; Berg, Å.; Bernard, H.; Berry, N.J.; Bhatt, D.; Bicknell, J.E.; Bihn, J.H.; Blake, R.J.; Bobo, K.S.; Bóçon, R.; Boekhout, T.; Böhning-Gaese, K.; Bonham, K.J.; Borges, P.A.V.; Borges, S.H.; Boutin, C.; Bouyer, J.; Bragagnolo, C.; Brandt, J.S.; Brearley, F.Q.; Brito, I.; Bros, V.; Brunet, J.; Buczkowski, G.; Buddle, C.M.; Bugter, R.; Buscardo, E.; Buse, J.; Cabra-García, J.; Cáceres, N.C.; Cagle, N.L.; Calviño-Cancela, M.; Cameron, S.A.; Cancello, E.M.; Caparrós, R.; Cardoso, P.; Carpenter, D.; Carrijo, T.F.; Carvalho, A.L.; Cassano, C.R.; Castro, H.; Castro-Luna, A.A.; Rolando, C.B.; Cerezo, A.; Chapman, K.A.; Chauvat, M.; Christensen, M.; Clarke, F.M.; Cleary, D.F.R.; Colombo, G.; Connop, S.P.; Craig, M.D.; Cruz-López, L.; Cunningham, S.A.; D'Aniello, B.; D'Cruze, N.; da Silva, P.G.; Dallimer, M.; Danquah, E.; Darvill, B.; Dauber, J.; Davis, A.L.V.; Dawson, J.; de Sassi, C.; de Thoisy, B.; Deheuvels, O.; Dejean, A.; Devineau, J.-L.; Diekötter, T.; Dolia, J.V.; Domínguez, E.; Dominguez-Haydar, Y.; Dorn, S.; Draper, I.; Dreber, N.; Dumont, B.; Dures, S.G.; Dynesius, M.; Edenius, L.; Eggleton, P.; Eigenbrod, F.; Elek, Z.; Entling, M.H.; Esler, K.J.; de Lima, R.F.; Faruk, A.; Farwig, N.; Fayle, T.M.; Felicioli, A.; Felton, A.M.; Fensham, R.J.; Fernandez, I.C.; Ferreira, C.C.; Ficetola, G.F.; Fiera, C.; Filgueiras, B.K.C.; Fırıncıoğlu, H.K.; Flaspohler, D.; Floren, A.; Fonte, S.J.; Fournier, A.; Fowler, R.E.; Franzén, M.; Fraser, L.H.; Fredriksson, G.M.; Freire, G.B., Jr.; Frizzo, T.L.M.; Fukuda, D.; Furlani, D.; Gaigher, R.; Ganzhorn, J.U.; García, K.P.; Garcia-R, J.C.; Garden, J.G.; Garilleti, R.; Ge, B.-M.; Gendreau-Berthiaume, B.; Gerard, P.J.; Gheler-Costa, C.; Gilbert, B.; Giordani, P.; Giordano, S.; Golodets, C.; Gomes, L.G.L.; Gould, R.K.; Goulson, D.; Gove, A.D.; Granjon, L.; Grass, I.; Gray, C.L.; Grogan, J.; Gu, W.; Guardiola, M.; Gunawardene, N.R.; Gutierrez, A.G.; Gutiérrez-Lamus, D.L.; Haarmeyer, D.H.; Hanley, M.E.; Hanson, T.; Hashim, N.R.; Hassan, S.N.; Hatfield, R.G.; Hawes, J.E.; Hayward, M.W.; Hébert, C.; Helden, A.J.; Henden, J.-A.; Henschel, P.; Hernández, L.; Herrera, J.P.; Herrmann, F.; Herzog, F.; Higuera-Diaz, D.; Hilje, B.; Höfer, H.; Hoffmann, A.; Horgan, F.G.; Hornung, E.; Horváth, R.; Hylander, K.; Isaacs-Cubides, P.; Ishida, H.; Ishitani, M.; Jacobs, C.T.; Jaramillo, V.J.; Jauker, B.; Hernández, F.J.; Johnson, M.F.; Jolli, V.; Jonsell, M.; Juliani, S.N.; Jung, T.S.; Kapoor, V.; Kappes, H.; Kati, V.; Katovai, E.; Kellner, K.; Kessler, M.; Kirby, K.R.; Kittle, A.M.; Knight, M.E.; Knop, E.; Kohler, F.; Koivula, M.; Kolb, A.; Kone, M.; Kőrösi, Á.; Krauss, J.; Kumar, A.; Kumar, R.; Kurz, D.J.; Kutt, A.S.; Lachat, T.; Lantschner, V.; Lara, F.; Lasky, J.R.; Latta, S.C.; Laurance, W.F.; Lavelle, P.; Le Féon, V.; LeBuhn, G.; Légaré, J.-P.; Lehouck, V.; Lencinas, M.V.; Lentini, P.E.; Letcher, S.G.; Li, Q.; Litchwark, S.A.; Littlewood, N.A.; Liu, Y.; Lo-Man-Hung, N.; López-Quintero, C.A.; Louhaichi, M.; Lövei, G.L.; Lucas-Borja, M.E.; Luja, V.H.; Luskin, M.S.; MacSwiney G, M.C.; Maeto, K.; Magura, T.; Mallari, N.A.; Malone, L.A.; Malonza, P.K.; Malumbres-Olarte, J.; Mandujano, S.; Måren, I.E.; Marin-Spiotta, E.; Marsh, C.J.; Marshall, E.J.P.; Martínez, E.; Martínez Pastur, G.; Moreno Mateos, D.; Mayfield, M.M.; Mazimpaka, V.; McCarthy, J.L.; McCarthy, K.P.; McFrederick, Q.S.; McNamara, S.; Medina, N.G.; Medina, R.; Mena, J.L.; Mico, E.; Mikusinski, G.; Milder, J.C.; Miller, J.R.; Miranda-Esquivel, D.R.; Moir, M.L.; Morales, C.L.; Muchane, M.N.; Muchane, M.; Mudri-Stojnic, S.; Munira, A.N.; Muoñz-Alonso, A.; Munyekenye, B.F.; Naidoo, R.; Naithani, A.; Nakagawa, M.; Nakamura, A.; Nakashima, Y.; Naoe, S.; Nates-Parra, G.; Navarrete Gutierrez, D.A.; Navarro-Iriarte, L.; Ndang'ang'a, P.K.; Neuschulz, E.L.; Ngai, J.T.; Nicolas, V.; Nilsson, S.G.; Noreika, N.; Norfolk, O.; Noriega, J.A.; Norton, D.A.; Nöske, N.M.; Nowakowski, A.J.; Numa, C.; O'Dea, N.; O'Farrell, P.J.; Oduro, W.; Oertli, S.; Ofori-Boateng, C.; Oke, C.O.; Oostra, V.; Osgathorpe, L.M.; Otavo, S.E.; Page, N.V.; Paritsis, J.; Parra-H, A.; Parry, L.; Pe'er, G.; Pearman, P.B.; Pelegrin, N.; Pélissier, R.; Peres, C.A.; Peri, P.L.; Persson, A.S.; Petanidou, T.; Peters, M.K.; Pethiyagoda, R.S.; Phalan, B.; Philips, T.K.; Pillsbury, F.C.; Pincheira-Ulbrich, J.; Pineda, E.; Pino, J.; Pizarro-Araya, J.; Plumptre, A.J.; Poggio, S.L.; Politi, N.; Pons, P.; Poveda, K.; Power, E.F.; Presley, S.J.; Proença, V.; Quaranta, M.; Quintero, C.; Rader, R.; Ramesh, B.R.; Ramirez-Pinilla, M.P.; Ranganathan, J.; Rasmussen, C.; Redpath-Downing, N.A.; Reid, J.L.; Reis, Y.T.; Rey Benayas, J.M.; Rey-Velasco, J.C.; Reynolds, C.; Ribeiro, D.B.; Richards, M.H.; Richardson, B.A.; Richardson, M.J.; Ríos, R.M.; Robinson, R.; Robles, C.A.; Römbke, J.; Romero-Duque, L.P.; Rös, M.; Rosselli, L.; Rossiter, S.J.; Roth, D.S.; Roulston, T.H.; Rousseau, L.; Rubio, A.V.; Ruel, J.-C.; Sadler, J.P.; Sáfián, S.; Saldaña-Vázquez, R.A.; Sam, K.; Samnegård, U.; Santana, J.; Santos, X.; Savage, J.; Schellhorn, N.A.; Schilthuizen, M.; Schmiedel, U.; Schmitt, C.B.; Schon, N.L.; Schüepp, C.; Schumann, K.; Schweiger, O.; Scott, D.M.; Scott, K.A.; Sedlock, J.L.; Seefeldt, S.S.; Shahabuddin, G.; Shannon, G.; Sheil, D.; Sheldon, F.H.; Shochat, E.; Siebert, S.J.; Silva, F.A.B.; Simonetti, J.A.; Slade, E.M.; Smith, J.; Smith-Pardo, A.H.; Sodhi, N.S.; Somarriba, E.J.; Sosa, R.A.; Soto Quiroga, G.; St-Laurent, M.-H.; Starzomski, B.M.; Stefanescu, C.; Steffan-Dewenter, I.; Stouffer, P.C.; Stout, J.C.; Strauch, A.M.; Struebig, M.J.; Su, Z.; Suarez-Rubio, M.; Sugiura, S.; Summerville, K.S.; Sung, Y.-H.; Sutrisno, H.; Svenning, J.-C.; Teder, T.; Threlfall, C.G.; Tiitsaar, A.; Todd, J.H.; Tonietto, R.K.; Torre, I.; Tóthmérész, B.; Tscharntke, T.; Turner, E.C.; Tylianakis, J.M.; Uehara-Prado, M.; Urbina-Cardona, N.; Vallan, D.; Vanbergen, A.J.; Vasconcelos, H.L.; Vassilev, K.; Verboven, H.A.F.; Verdasca, M.J.; Verdú, J.R.; Vergara, C.H.; Vergara, P.M.; Verhulst, J.; Virgilio, M.; Vu, L.V.; Waite, E.M.; Walker, T.R.; Wang, H.-F.; Wang, Y.; Watling, J.I.; Weller, B.; Wells, K.; Westphal, C.; Wiafe, E.D.; Williams, C.D.; Willig, M.R.; Woinarski, J.C.Z.; Wolf, J.H.D.; Wolters, V.; Woodcock, B.A.; Wu, J.; Wunderle, J.M., Jr.; Yamaura, Y.; Yoshikura, S.; Yu, D.W.; Zaitsev, A.S.; Zeidler, J.; Zou, F.; Collen, B.; Ewers, R.M.; Mace, G.M.; Purves, D.W.; Scharlemann, J.P.W.; Purvis, A. pdf  url
doi  openurl
  Title (down) The database of the PREDICTS (Projecting Responses of Ecological Diversity In Changing Terrestrial Systems) project Type Journal Article
  Year 2017 Publication Ecology and Evolution Abbreviated Journal Ecology and Evolution  
  Volume 7 Issue 1 Pages 145-188  
  Keywords data sharing; global biodiversity modeling; global change; habitat destruction; land use  
  Abstract The PREDICTS project—Projecting Responses of Ecological Diversity In Changing Terrestrial Systems (www.predicts.org.uk)—has collated from published studies a large, reasonably representative database of comparable samples of biodiversity from multiple sites that differ in the nature or intensity of human impacts relating to land use. We have used this evidence base to develop global and regional statistical models of how local biodiversity responds to these measures. We describe and make freely available this 2016 release of the database, containing more than 3.2 million records sampled at over 26,000 locations and representing over 47,000 species. We outline how the database can help in answering a range of questions in ecology and conservation biology. To our knowledge, this is the largest and most geographically and taxonomically representative database of spatial comparisons of biodiversity that has been collated to date; it will be useful to researchers and international efforts wishing to model and understand the global status of biodiversity. © 2016 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.  
  Address Computational Ecology and Environmental Science, Microsoft Research, Cambridge, United Kingdom  
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  Notes Export Date: 17 January 2017 Approved no  
  Call Number EcoFoG @ webmaster @ Serial 705  
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Author Maia, A.C.D.; Gibernau, M.; Carvalho, A.T.; Gonçalves, E.G.; Schlindwein, C. url  openurl
  Title (down) The cowl does not make the monk: Scarab beetle pollination of the Neotropical aroid Taccarum ulei (Araceae: Spathicarpeae) Type Journal Article
  Year 2013 Publication Biological Journal of the Linnean Society Abbreviated Journal  
  Volume 108 Issue 1 Pages 22-34  
  Keywords Flower predation; Nocturnal pollinators; Pollination syndromes; Scarabaeidae; Thermogenesis  
  Abstract Taccarum ulei (Araceae, Spathicarpeae) is a seasonal geophytic aroid, native to north-eastern Brazil, that flowers during two months of the rainy season. Patterns of floral thermogenesis, pollination biology, and floral traits associated with pollination syndromes were studied and compared with those of other Araceae. Two species of cyclocephaline scarabs (Scarabaeidae, Cyclocephalini) were recognized as effective pollinators: Cyclocephala celata and Cyclocephala cearae. Larvae of an unidentified species of fruit fly (Melanolomaspp., Richardiidae, Diptera) were also frequently observed in inflorescences at various maturation stages, feeding on the connectives of male florets and fruits, and thus lowering the reproductive success of individual plants. Beetles were attracted by odoriferous inflorescences in the early evening of the first day of anthesis, during the female phase. The emission of attractive volatiles was coupled with intense thermogenic activity in the entire spadix, unlike other aroids in which only certain zones of the spadix heat up. Pollen release, which marks the beginning of the male phase on the subsequent evening, was not related to floral thermogenesis. Comparative multivariate analysis of the floral traits of T.ulei points to a beetle-pollinated aroid, although some of the observed traits of the species are not common to other taxa sharing this pollination strategy. Such incongruence might be explained by the evolutionary history of the tribe Spathicarpeae and potential pollinator shifts. © 2012 The Linnean Society of London.  
  Address Departamento de Botânica, Universidade Federal de Minas Gerais, Belo Horizonte, 31270-901, Brazil  
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  Notes Export Date: 3 January 2013; Source: Scopus Approved no  
  Call Number EcoFoG @ webmaster @ Serial 453  
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Author Leroy, C.; Carrias, J.-F.; Céréghino, R.; Corbara, B. url  doi
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  Title (down) The contribution of microorganisms and metazoans to mineral nutrition in bromeliads Type Journal Article
  Year 2016 Publication Journal of Plant Ecology Abbreviated Journal Journal of Plant Ecology  
  Volume 9 Issue 3 Pages 241-255  
  Keywords digestive mutualism; insect-assisted nutrients; leaf δ15N; multiple N sources; myrmecotrophy  
  Abstract Aims One critical challenge for plants is to maintain an adequate nutrient supply under fluctuating environmental conditions. This is particularly true for epiphytic species that have limited or no access to the pedosphere and often live in harsh climates. Bromeliads have evolved key innovations such as epiphytism, water-absorbing leaf trichomes, tank habit and Crassulacean acid metabolism (CAM) photosynthesis that enable them to survive under various environmental conditions. Bromeliads encompass diverse ecological types that live on different substrates (they can be terrestrial, epilithic or epiphytic) and vary in their ability to retain water (they can be tank-forming or tankless) and photosynthetic pathway (i.e. C3 or CAM). In this review, we outline the nutritional modes and specializations that enable bromeliads to thrive in a wide range of nutrient-poor (mostly nitrogen-depleted) environments. Important Findings Bromeliads have evolved a great diversity of morphologies and functional adaptations leading to the existence of numerous nutritional modes. Focusing on species that have absorptive foliar trichomes, we review evidence that bromeliads have evolved multi-faceted nutritional strategies to respond to fluctuations in the supply of natural nitrogen (N). These plants have developed mutualistic associations with many different and functionally diverse terrestrial and aquatic microorganisms and metazoans that contribute substantially to their mineral nutrition and, thus, their fitness and survival. Bacterial and fungal microbiota-assisted N provisioning, protocarnivory, digestive mutualisms and myrmecotrophic pathways are the main strategies used by bromeliads to acquire nitrogen. The combination of different nutritional pathways in bromeliads represents an important adaptation enabling them to exploit nutrient-poor habitats. Nonetheless, as has been shown for several other vascular plants, multiple partners are involved in nutrient acquisition indicating that there have been convergent adaptations to nutrient scarcity. Finally, we point out some gaps in the current knowledge of bromeliad nutrition that offer fascinating research opportunities. © The Author 2015. Published by Oxford University Press on behalf of the Institute of Botany, Chinese Academy of Sciences and the Botanical Society of China.  
  Address CNRS, EcoLab, 118 Route de Narbonne, Toulouse, France  
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  Notes Export Date: 28 June 2016 Approved no  
  Call Number EcoFoG @ webmaster @ Serial 683  
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Author Seibold, Sebastien ; Rammer, Werner ; Hothorn, Torsten ; Seidl, Rupert ; Ulyshen, Michael ; Lorz, Janina ; Cadotte, Marc ; Lindenmayer, David ; Adhikari, Yagya ; Aragón, Roxana ; Bae, Soyeon ; Baldrian, Petr ; Barimani Varandi, Hassan ; Barlow, Jos ; Bässler, Clauss ; Beauchêne, Jacques ; and all ................... doi  openurl
  Title (down) The contribution of insects to global forest deadwood decomposition Type Journal Article
  Year 2021 Publication Nature Abbreviated Journal  
  Volume 597 Issue 7874 Pages 77-81  
  Keywords  
  Abstract The amount of carbon stored in deadwood is equivalent to about 8 per cent of the global forest carbon stocks1. The decomposition of deadwood is largely governed by climate2-5 with decomposer groups-such as microorganisms and insects-contributing to variations in the decomposition rates2,6,7. At the global scale, the contribution of insects to the decomposition of deadwood and carbon release remains poorly understood7. Here we present a field experiment of wood decomposition across 55 forest sites and 6 continents. We find that the deadwood decomposition rates increase with temperature, and the strongest temperature effect is found at high precipitation levels. Precipitation affects the decomposition rates negatively at low temperatures and positively at high temperatures. As a net effect-including the direct consumption by insects and indirect effects through interactions with microorganisms-insects accelerate the decomposition in tropical forests (3.9% median mass loss per year). In temperate and boreal forests, we find weak positive and negative effects with a median mass loss of 0.9 per cent and -0.1 per cent per year, respectively. Furthermore, we apply the experimentally derived decomposition function to a global map of deadwood carbon synthesized from empirical and remote-sensing data, obtaining an estimate of 10.9 ± 3.2 petagram of carbon per year released from deadwood globally, with 93 per cent originating from tropical forests. Globally, the net effect of insects may account for 29 per cent of the carbon flux from deadwood, which suggests a functional importance of insects in the decomposition of deadwood and the carbon cycle.  
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  Publisher NATURE PUBLISHING GROUP Place of Publication Editor  
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  Call Number EcoFoG @ webmaster @ Serial 1046  
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Author Touchard, A.; Koh, J.M.S.; Aili, S.R.; Dejean, A.; Nicholson, G.M.; Orivel, J.; Escoubas, P. url  openurl
  Title (down) The complexity and structural diversity of ant venom peptidomes is revealed by mass spectrometry profiling Type Journal Article
  Year 2015 Publication Rapid Communications in Mass Spectrometry Abbreviated Journal Rapid Communications in Mass Spectrometry  
  Volume 29 Issue 5 Pages 385-396  
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  Abstract Rationale Compared with other animal venoms, ant venoms remain little explored. Ants have evolved complex venoms to rapidly immobilize arthropod prey and to protect their colonies from predators and pathogens. Many ants have retained peptide-rich venoms that are similar to those of other arthropod groups. Methods With the goal of conducting a broad and comprehensive survey of ant venom peptide diversity, we investigated the peptide composition of venoms from 82 stinging ant species from nine subfamilies using matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOFMS). We also conducted an in-depth investigation of eight venoms using reversed-phase high-performance liquid chromatography (RP-HPLC) separation coupled with offline MALDI-TOFMS. Results Our results reveal that the peptide compositions of ant venom peptidomes from both poneroid and formicoid ant clades comprise hundreds of small peptides (<4 kDa), while large peptides (>4 kDa) are also present in the venom of formicoids. Chemical reduction revealed the presence of disulfide-linked peptides in most ant subfamilies, including peptides structured by one, two or three disulfide bonds as well as dimeric peptides reticulated by three disulfide bonds. Conclusions The biochemical complexity of ant venoms, associated with an enormous ecological and taxonomic diversity, suggests that stinging ant venoms constitute a promising source of bioactive molecules that could be exploited in the search for novel drug and biopesticide leads. Copyright © 2015 John Wiley & Sons, Ltd. Copyright © 2015 John Wiley & Sons, Ltd.  
  Address VenomeTech, 473 Route des DolinesValbonne, France  
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  Notes Export Date: 24 April 2015 Approved no  
  Call Number EcoFoG @ webmaster @ Serial 599  
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Author Longo, M.; Knox, R.G.; Levine, N.M.; Swann, A.L.S.; Medvigy, D.M.; Dietze, M.C.; Kim, Y.; Zhang, K.; Bonal, D.; Burban, B.; Camargo, P.B.; Hayek, M.N.; Saleska, S.R.; Da Silva, R.; Bras, R.L.; Wofsy, S.C.; Moorcroft, P.R. pdf  url
doi  openurl
  Title (down) The biophysics, ecology, and biogeochemistry of functionally diverse, vertically and horizontally heterogeneous ecosystems: The Ecosystem Demography model, version 2.2-Part 2: Model evaluation for tropical South America Type Journal Article
  Year 2019 Publication Geoscientific Model Development Abbreviated Journal Geoscientific Model Dev.  
  Volume 12 Issue 10 Pages 4347-4374  
  Keywords  
  Abstract The Ecosystem Demography model version 2.2 (ED-2.2) is a terrestrial biosphere model that simulates the biophysical, ecological, and biogeochemical dynamics of vertically and horizontally heterogeneous terrestrial ecosystems. In a companion paper (Longo et al., 2019a), we described how the model solves the energy, water, and carbon cycles, and verified the high degree of conservation of these properties in long-term simulations that include long-term (multi-decadal) vegetation dynamics. Here, we present a detailed assessment of the model's ability to represent multiple processes associated with the biophysical and biogeochemical cycles in Amazon forests. We use multiple measurements from eddy covariance towers, forest inventory plots, and regional remote-sensing products to assess the model's ability to represent biophysical, physiological, and ecological processes at multiple timescales, ranging from subdaily to century long. The ED-2.2 model accurately describes the vertical distribution of light, water fluxes, and the storage of water, energy, and carbon in the canopy air space, the regional distribution of biomass in tropical South America, and the variability of biomass as a function of environmental drivers. In addition, ED-2.2 qualitatively captures several emergent properties of the ecosystem found in observations, specifically observed relationships between aboveground biomass, mortality rates, and wood density; however, the slopes of these relationships were not accurately captured. We also identified several limitations, including the model's tendency to overestimate the magnitude and seasonality of heterotrophic respiration and to overestimate growth rates in a nutrient-poor tropical site. The evaluation presented here highlights the potential of incorporating structural and functional heterogeneity within biomes in Earth system models (ESMs) and to realistically represent their impacts on energy, water, and carbon cycles. We also identify several priorities for further model development.  
  Address Georgia Institute of Technology, Atlanta, GA, United States  
  Corporate Author Thesis  
  Publisher Copernicus GmbH Place of Publication Editor  
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  ISSN 1991959x (Issn) ISBN Medium  
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  Notes Cited By :1; Export Date: 27 October 2019; Correspondence Address: Longo, M.; Harvard UniversityUnited States; email: mdplongo@gmail.com Approved no  
  Call Number EcoFoG @ webmaster @ Serial 890  
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Author Touchard, A.; Aili, S.R.; Fox, E.G.P.; Escoubas, P.; Orivel, J.; Nicholson, G.M.; Dejean, A. pdf  url
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  Title (down) The biochemical toxin arsenal from ant venoms Type Journal Article
  Year 2016 Publication Toxins Abbreviated Journal Toxins  
  Volume 8 Issue 1 Pages 30  
  Keywords Alkaloids; Ant venom; Enzymes; Formic acid; Peptides; Toxins; Venom biochemistry  
  Abstract Ants (Formicidae) represent a taxonomically diverse group of hymenopterans with over 13,000 extant species, the majority of which inject or spray secretions from a venom gland. The evolutionary success of ants is mostly due to their unique eusociality that has permitted them to develop complex collaborative strategies, partly involving their venom secretions, to defend their nest against predators, microbial pathogens, ant competitors, and to hunt prey. Activities of ant venom include paralytic, cytolytic, haemolytic, allergenic, pro-inflammatory, insecticidal, antimicrobial, and pain-producing pharmacologic activities, while non-toxic functions include roles in chemical communication involving trail and sex pheromones, deterrents, and aggregators. While these diverse activities in ant venoms have until now been largely understudied due to the small venom yield from ants, modern analytical and venomic techniques are beginning to reveal the diversity of toxin structure and function. As such, ant venoms are distinct from other venomous animals, not only rich in linear, dimeric and disulfide-bonded peptides and bioactive proteins, but also other volatile and non-volatile compounds such as alkaloids and hydrocarbons. The present review details the unique structures and pharmacologies of known ant venom proteinaceous and alkaloidal toxins and their potential as a source of novel bioinsecticides and therapeutic agents. © 2016 by the authors; licensee MDPI, Basel, Switzerland.  
  Address Laboratoire Écologie Fonctionnelle et Environnement, 118 Route de Narbonne, Toulouse, France  
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  Notes Export Date: 8 February 2016 Approved no  
  Call Number EcoFoG @ webmaster @ Serial 656  
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Author Dejean, A.; Corbara, B.; Roux, O.; Orivel, J. url  openurl
  Title (down) The antipredatory behaviours of neotropical ants towards army ant raids (Hymenoptera: Formicidae) Type Journal Article
  Year 2014 Publication Myrmecological News Abbreviated Journal Myrmecological News  
  Volume 19 Issue Pages 17-24  
  Keywords Antipredatory behaviour; Army ants; Ecitoninae; Prey-ant species  
  Abstract Group hunting, nomadism, wingless queens and colony fission characterize army ants, allowing them to have become the main tropical arthropod predators, mostly of other social insects. We studied the reactions of different ant species to the New World army ants Eciton burchellii (WESTWOOD, 1842) and E. hamatum (FABRICIUS, 1782) (Ecitoninae). We compiled our results with those already known in a synthetic appendix. A wide range of ant species react to the ap-proach of army ant raids by evacuating their nests with several workers transporting brood. The Eciton plunder a large part of the brood but rarely kill workers or queens, so that the latter return to their nest and resume colony activity. One exception is Paratrechina longicornis (LATREILLE, 1802) colonies that quickly evacuate their nest, so that the entire col-ony can generally escape a raid. Another is Leptogenys mexicana (MAYR, 1870) that leave their nests in columns while some nestmates resist the attack; they therefore lose only a few larvae. We noted that colonies can avoid being raided if the army ants ignore them (Atta cephalotes (LINNAEUS, 1758)), or if the workers produce a repellent substance (Azteca associated with myrmecophytic Cecropia) or are repellent themselves (Pachycondyla villosa (FABRICIUS, 1804), Ec-tatomma spp.). In the other cases, a part of the brood is lost. When an Eciton raid approached the base of their host-tree trunk, Azteca andreae GUERRERO, DELABIE and DEJEAN, 2010 workers dropped a part of their brood on the ground. While numerous Eciton workers were gathering up this brood, the front of the column advanced, so that the Azteca andreae nests were not plundered. Pheidole megacephala (FABRICIUS, 1793) nests were partly plundered as the workers reacted aggressively, blocking the Eciton inside their nests during a long time. When the latter returned toward their bivouac, they were attacked and killed by their nestmates whether or not they had retrieved Pheidole brood. Consequently, the front of the column turned away from the Pheidole nest.  
  Address Maladies Infectieuses et Vecteurs, Evolution et Contrôle (UMR- IRD 224) Équipe BEES, IRD 01, BP 171 Bobo-Dioulasso, Burkina Faso  
  Corporate Author Thesis  
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  ISSN 19944136 (Issn) ISBN Medium  
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  Notes Export Date: 10 March 2014; Source: Scopus; Language of Original Document: English; Correspondence Address: Dejean, A.; Écologie des Forêts de Guyane (UMR-CNRS 8172), Campus agronomique, BP 316, 97379 Kourou cedex, France; email: alain.dejean@wanadoo.fr Approved no  
  Call Number EcoFoG @ webmaster @ Serial 535  
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Author Rodrigues, A.M.S.; Eparvier, V.; Odonne, G.; Amusant, N.; Stien, D.; Houël, E. pdf  url
doi  openurl
  Title (down) The antifungal potential of (Z)-ligustilide and the protective effect of eugenol demonstrated by a chemometric approach Type Journal Article
  Year 2019 Publication Scientific Reports Abbreviated Journal Sci. Rep.  
  Volume 9 Issue Pages 8729  
  Keywords  
  Abstract Mankind is on the verge of a postantibiotic era. New concepts are needed in our battle to attenuate infectious diseases around the world and broad spectrum plant-inspired synergistic pharmaceutical preparations should find their place in the global fight against pathogenic microorganisms. To progress towards the discovery of potent antifungal agents against human pathologies, we embarked upon developing chemometric approach coupled with statistical design to unravel the origin of the anticandidal potential of a set of 66 essential oils (EOs). EOs were analyzed by GC-MS and tested against Candida albicans and C. parapsilosis (Minimal Inhibitory Concentration, MIC). An Orthogonal Partial Least Square (OPLS) analysis allowed us to identify six molecules presumably responsible for the anticandidal activity of the oils: (Z)-ligustilide, eugenol, eugenyl acetate, citral, thymol, and β-citronellol. These compounds were combined following a full factorial experimental design approach in order to optimize the anticandidal activity and selectivity index (SI = IC50(MRC5 cells)/MIC) through reconstituted mixtures. (Z)-Ligustilide and citral were the most active compounds, while (Z)-ligustilide and eugenol were the two main factors that most contributed to the increase of the SI. These two terpenes can, therefore, be used to construct bioinspired synergistic anticandidal mixtures. © 2019, The Author(s).  
  Address CNRS, UMR EcoFoG, AgroParisTech, Cirad, INRA, Université des Antilles, Université de Guyane, Cayenne, 97300, France  
  Corporate Author Thesis  
  Publisher Nature Publishing Group Place of Publication Editor  
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  ISSN 20452322 (Issn) ISBN Medium  
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  Notes Approved no  
  Call Number EcoFoG @ webmaster @ Serial 876  
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Author Roy, M.; Vasco-Palacios, A.; Geml, J.; Buyck, B.; Delgat, L.; Giachini, A.; Grebenc, T.; Harrower, E.; Kuhar, F.; Magnago, A.; Rinaldi, A.C.; Schimann, H.; Selosse, M.-A.; Sulzbacher, M.A.; Wartchow, F.; Neves, M.-A. url  doi
openurl 
  Title (down) The (re)discovery of ectomycorrhizal symbioses in Neotropical ecosystems sketched in Florianópolis Type Journal Article
  Year 2017 Publication New Phytologist Abbreviated Journal New Phytologist  
  Volume 214 Issue 3 Pages 920-923  
  Keywords barcoding; biodiversity; ectomycorrhizal fungi; ectomycorrhizal roots; ectomycorrhizal symbioses; fruitbodies; Neotropical ecosystems  
  Abstract  
  Address Departamento de Sistemática e Ecologia/CCEN, Laboratório de Morfo-Taxonomia Fúngica, Universidade Federal da Paraíba, João Pessoa, Paraíba, Brazil  
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  Notes Cited By :1; Export Date: 23 April 2017 Approved no  
  Call Number EcoFoG @ webmaster @ Serial 749  
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