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Effects of phenotypic complementarity and phylogeny on the nested structure of mutualistic networks. (2007)

by E L Rezende
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The ecological and evolutionary implications of merging different types of networks

by Colin Fontaine , Paulo R Guimarã , Sonia Ké Jr , Nicolas Loeuille , Jane Memmott , Wim H Van Der Putten , Frank J F Van Veen , Elisa Thé Bault - Ecol. Lett , 2011
"... Abstract Interactions among species drive the ecological and evolutionary processes in ecological communities. These interactions are effectively key components of biodiversity. Studies that use a network approach to study the structure and dynamics of communities of interacting species have reveal ..."
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Abstract Interactions among species drive the ecological and evolutionary processes in ecological communities. These interactions are effectively key components of biodiversity. Studies that use a network approach to study the structure and dynamics of communities of interacting species have revealed many patterns and associated processes. Historically these studies were restricted to trophic interactions, although network approaches are now used to study a wide range of interactions, including for example the reproductive mutualisms. However, each interaction type remains studied largely in isolation from others. Merging the various interaction types within a single integrative framework is necessary if we want to further our understanding of the ecological and evolutionary dynamics of communities. Dividing the networks up is a methodological convenience as in the field the networks occur together in space and time and will be linked by shared species. Herein, we outline a conceptual framework for studying networks composed of more than one type of interaction, highlighting key questions and research areas that would benefit from their study.
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...o move forwards. THE ARCHITECTURE OF BIPARTITE NETWORKS VARIES ACCORDING TO THE TYPE AND INTIMACY OF THE INTERACTION CONSIDERED The determinants of network architecture An important body of work has looked for the determinants of network architecture. Most of the studies to date have looked for these in species traits such as body size in food webs (Woodward et al. 2005; Petchey et al. 2008), morphology and phenology in pollination networks (Stang et al. 2006; Olesen et al. 2008) or integrative proxies for species traits with the use of the evolutionary history of species (Cattin et al. 2004; Rezende et al. 2007a,b). It is becoming clear though that interaction characteristics (type and intimacy, Fig. 1A) could also affect the architecture of ecological networks. It has been proposed that antagonistic interactions should be more specific than mutualistic ones because the arms race between hosts and antagonists often leads to adaptation at the expense of the ability to attack alternative hosts (Thompson 1982; Nuismer & Thompson 2006), whereas species in mutualistic interactions are often specialised in traits shared by several species within a community resulting in enhanced generalism (Thompson 2005;...

Ecophylogenetics: advances and perspectives.

by Nicolas Mouquet , Vincent Devictor , Christine N Meynard , Francois Munoz , Louis-Félix Bersier , Jérôme Chave , Pierre Couteron , Ambroise Dalecky , Colin Fontaine , Dominique Gravel , Olivier J Hardy , Franck Jabot , Sébastien Lavergne , Mathew Leibold , David Mouillot , Tamara Münkemüller , Sandrine Pavoine , Andreas Prinzing , Ana S L Rodrigues , Rudolf P Rohr , Elisa Thébault , Wilfried Thuiller - Biol. Rev. , 2012
"... ABSTRACT Ecophylogenetics can be viewed as an emerging fusion of ecology, biogeography and macroevolution. This new and fastgrowing field is promoting the incorporation of evolution and historical contingencies into the ecological research agenda through the widespread use of phylogenetic data. Inc ..."
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ABSTRACT Ecophylogenetics can be viewed as an emerging fusion of ecology, biogeography and macroevolution. This new and fastgrowing field is promoting the incorporation of evolution and historical contingencies into the ecological research agenda through the widespread use of phylogenetic data. Including phylogeny into ecological thinking represents an opportunity for biologists from different fields to collaborate and has provided promising avenues of research in both theoretical and empirical ecology, towards a better understanding of the assembly of communities, the functioning of ecosystems and their responses to environmental changes. The time is ripe to assess critically the extent to which the integration of phylogeny into these different fields of ecology has delivered on its promise. Here we review how phylogenetic information has been used to identify better the key components of species interactions with their biotic and abiotic environments, to determine the relationships between diversity and ecosystem functioning and ultimately to establish good management practices to protect overall biodiversity in the face of global change. We evaluate the relevance of information provided by phylogenies to ecologists, highlighting current potential weaknesses and needs for future developments. We suggest
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...ifically designed to find a phylogenetic signal in bipartite networks based on a generalized least-square model. These studies generally focus on local interaction networks and they show that, indeed, phylogenetically similar species tend to interact with the same set of species and/or tend to occupy similar structural positions in the network (i.e. species having similar specialization or belonging to the same compartment). This has been shown in food webs (Cattin et al., 2004; Bersier & Kehrli, 2008), in host-parasitoid networks (Ives & Godfray, 2006), in frugivory and pollination networks (Rezende et al., 2007b) and plant-plant facilitation networks (Verdu & Valiente-Banuet, 2011). A BMatrix of similarity in interaction between species vs Species traits vs related to network structure Fig. 3. Interaction networks and phylogenetic signal. There are two main methods to assess phylogenetic signal in networks. (A) By relating phylogenetic similarity with the similarity the identity of interacting partners. Simple Mantel tests can be used to relate phylogenetic similarity with the similarity in interactions for species in the network. Similarity in interaction between two species is generally measured b...

A neutralniche theory of nestedness in mutualistic networks.

by Abhay Krishna , Paulo R Guimarães Jr , Pedro Jordano , Jordi Bascompte , abhay@ebd.csic.es A Krishna , P R Guimarães Jr , P Jordano , J Bascompte - Oikos, , 2008
"... Recently, there has been a vigorous interest in community ecology about the structure of mutualistic networks and its importance for species persistence and coevolution. However, the mechanisms shaping mutualistic networks have been rarely explored. Here we extend for the first time the neutral the ..."
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Recently, there has been a vigorous interest in community ecology about the structure of mutualistic networks and its importance for species persistence and coevolution. However, the mechanisms shaping mutualistic networks have been rarely explored. Here we extend for the first time the neutral theory of biodiversity to a multi trophic system. We focus on nestedness, a distinctive pattern of mutualistic community assembly showing two characteristics, namely, asymmetrical specialization (specialists interacting with generalists) and a generalist core (generalists interacting with generalists). We investigate the importance of relative species abundance (RSA) for the nested assembly of plantÁanimal mutualistic networks. Our results show that neutral mutualistic communities give rise to networks considerably more nested than real communities. RSA explains 60Á70% of nested patterns in two real communities studied here, while 30Á40% of nestedness is still unexplained. The nested pattern in real communities is better explained when we introduce interactionspecific species traits such as forbidden links and intensity of dependence (relative importance of fruits for the diet of a frugivore) in our analysis. The fact that neutral mutualistic communities exhibit a perfectly nested structure and do not show a random or compartmentalized structure, underlines the importance of RSA in the assembly of mutualistic networks. Recent studies demonstrate that mutualisms among free living species often form nested networks, i.e. those species with fewer interactions are preferentially associated with a subset of species that interact with the most connected ones (Bascompte et al.

Abstract Probabilistic Modelling of the Evolution of Ecological Interaction Networks

by Henintsoa Onivola Minoarivelo, Supervisor Prof, H. O. Minoarivelo, H. O. Minoarivelo , 2011
"... By submitting this thesis electronically, I declare that the entirety of the work contained therein is my own, original work, that I am the owner of the copyright thereof (unless to the extent explicitly otherwise stated) and that I have not previously in its entirety or in part submitted it for obt ..."
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By submitting this thesis electronically, I declare that the entirety of the work contained therein is my own, original work, that I am the owner of the copyright thereof (unless to the extent explicitly otherwise stated) and that I have not previously in its entirety or in part submitted it for obtaining any qualification.

rspb.royalsocietypublishing.org

by Bromeliaceae Chamela-cuixmala Biosphere, Martha Lopezaraiza-mikel , 2012
"... reserve, ecological interactions, Mexico, Evaluating factors that predict the largely predicted pairwise interactions and several network metrics. Wood density and bark texture of hosts also contributed to explain network struc-on September 15, ..."
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reserve, ecological interactions, Mexico, Evaluating factors that predict the largely predicted pairwise interactions and several network metrics. Wood density and bark texture of hosts also contributed to explain network struc-on September 15,
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...oyalsocietypublishing.org/Downloaded from signal. Additionally, if traits important for species associations are phylogenetically conserved, then phylogeny will indirectly influence network structure =-=[62,63]-=-. Abundance does not show a phylogenetic signal in the epiphyte or phorophyte assemblage (see the electronic supplementary material, table S2 and figure S4). Wood density is highly conserved across th...

hummingbird-pollinated

by Sjirk Geerts, Anton Pauw
"... sunbirds hover to pollinate an invasive ..."
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sunbirds hover to pollinate an invasive

unknown title

by unknown authors
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...Sukhdeo, 2008; Lafferty et al., 2006). Indeed, a number of sources highlight the importance of a variety of simultaneous mechanism leading to nestedness (Bastolla et al., 2009; Fontaine et al., 2009; =-=Rezende et al., 2007-=-; Vázquez et al., 2009a). Krishna et al. (2008) even demonstrate that, although abundance and trait matching separately can be seen to influence nestedness, considering the two together provides a fa...

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by unknown authors
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unknown title

by Kazuhiro Takemoto A, Masanori Arita A
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...text (e.g., geographic and temporal variation). The structure of interactions between plants and animals may be affected by not only species traits and external factors but also evolutionary history (=-=Rezende et al., 2007-=-a). Thus far, few efforts have been made to theoretically explain the development of interactions between plants and animals. For example, Rezende et al. (2007b) showed that plant-animal mutualistic n...

Co-evolution of resource trade-offs driving species interactions in a

by unknown authors
"... host-parasite network: An exploratory model ..."
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host-parasite network: An exploratory model
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...nfects (Lewinsohn et al., 2006; Poulin, 2007). This does not, for example, explain the frequent occurrence of anti-nestedness. Further explanations for nestedness in networks include complementarity (=-=Rezende et al., 2007-=-), based on phenotypic matching between species, and competitive load (Bastolla et al., 2009), based on a new species entering a network targeting a host with less competition provided by resident par...

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