UMA ESTRATÉGIA UNIFICADA PARA A ESTIMATIVA DE COMPONENTES ESPACIAIS, TEMPORAIS E FILOGENÉTICOS EM MODELOS ECOLÓGICOS

The goals of this paper are to expose ecologists to the problem related to statistical inference when testing the association between data sets that are autocorrelated and to introduce a relatively new method for controlling the bias introduced by autocorrelation that can be easily incorporated in any statistical approach. In addition, I show the flexibility of this class of methods to the types of data that ecologists are currently most interested, namely temporal, spatial and phylogenetic data. In this contribution, I also stress the point that is not all variation due to autocorrelation that affects statistical inference and is important to control only the component that biases inference. Thus, statistical frameworks should attempt to separate the autocorrelation component that biases inference from the one that may prove interesting for understanding important ecological processes, such as contagious processes, driving spatial patterns in species distributions.O objetivo deste trabalho é de expor aos ecólogos o problema relacionado aos testes de inferência estatística quando os dados são autocorrelacionados e apresentar uma técnica relativamente nova que pode ser facilmente incorporada em análises estatísticas para controlar os erros causados pela autocorrelação. Além disso, eu demonstro a flexibilidade deste método utilizando três tipos de dados que são importantes em análises ecológicas: dados temporais, espaciais e filogenéticos. Neste trabalho, eu reitero que não é toda a variação autocorrelacionada que afeta as inferências estatísticas e que é importante controlar apenas o componente de variação reponsável. Assim, análises estatísticas devem ser realizadas com o objetivo de separar o componente de variação autocorrelacionada -- que causa erros em testes de hipóteses -- do componente que pode ser importante para a compreensão de processos ecológicos, como processos contagiosos (e.g., dispersão), estruturando padrões de distribuição espacial em espécies

Inferring explicit weighted consensus networks to represent alternative evolutionary histories

Background: The advent of molecular biology techniques and constant increase in availability of genetic material have triggered the development of many phylogenetic tree inference methods. However, several reticulate evolution processes, such as horizontal gene transfer and hybridization, have been shown to blur the species\ud evolutionary history by causing discordance among phylogenies inferred from different genes.\ud Methods: To tackle this problem, we hereby describe a new method for inferring and representing alternative(reticulate) evolutionary histories of species as an explicit weighted consensus network which can be constructed from a collection of gene trees with or without prior knowledge of the species phylogeny.\ud Results: We provide a way of building a weighted phylogenetic network for each of the following reticulation\ud mechanisms: diploid hybridization, intragenic recombination and complete or partial horizontal gene transfer. We successfully tested our method on some synthetic and real datasets to infer the above-mentioned evolutionary events which may have influenced the evolution of many species.\ud Conclusions: Our weighted consensus network inference method allows one to infer, visualize and validate statistically major conflicting signals induced by the mechanisms of reticulate evolution. The results provided by the new method can be used to represent the inferred conflicting signals by means of explicit and easy-to-interpret phylogenetic networks

The Interaction of Phylogeny and Community Structure: Linking the Community Composition and Trait Evolution of Clades

Aim Community phylogenetic studies use information about the evolutionary relationships of species to understand the ecological processes of community assembly. A central premise of the field is that the evolution of species maps onto ecological patterns, and phylogeny reveals something more than species traits alone about the ecological mechanisms structuring communities, such as environmental filtering, competition, and facilitation. We argue, therefore, that there is a need for better understanding and modelling of the interaction of phylogeny with species traits and community composition. Innovation We outline a new approach that identifies clades that are ecophylogenetically clustered or overdispersed and assesses whether those clades have different rates of trait evolution. Ecophylogenetic theory would predict that the traits of clustered or overdispersed clades might have evolved differently, in terms of either tempo (fast or slow) or mode (e.g., under constraint or neutrally). We suggest that modelling the evolution of independent trait data in these clades represents a strong test of whether there is an association between the ecological co‐occurrence patterns of a species and its evolutionary history. Main conclusions Using an empirical dataset of mammals from around the world, we identify two clades of rodents whose species tend not to co‐occur in the same local assemblages (are phylogenetically overdispersed) and find independent evidence of slower rates of body mass evolution in these clades. Our approach, which assumes nothing about the mode of species trait evolution but instead seeks to explain it using ecological information, presents a new way to examine ecophylogenetic structure

Towards an applied metaecology

The complexity of ecological systems is a major challenge for practitioners and decision-makers who work to avoid, mitigate and manage environmental change. Here, we illustrate how metaecology – the study of spatial interdependencies among ecological systems through fluxes of organisms, energy, and matter – can enhance understanding and improve managing environmental change at multiple spatial scales. We present several case studies illustrating how the framework has leveraged decision-making in conservation, restoration and risk management. Nevertheless, an explicit incorporation of metaecology is still uncommon in the applied ecology literature, and in action guidelines addressing environmental change. This is unfortunate because the many facets of environmental change can be framed as modifying spatial context, connectedness and dominant regulating processes - the defining features of metaecological systems. Narrowing the gap between theory and practice will require incorporating system-specific realism in otherwise predominantly conceptual studies, as well as deliberately studying scenarios of environmental change.We thank FAPESP (grants 2014/10470-7 to AM, 2013/04585-3 to DL, 2013/50424-1 to TS and 2015/18790-3to LS), CNPq (Productivity Fellowships 301656/2011-8 to JAFDF,308205/2014-6 to RP, 306183/2014-5 to PIP and 307689/2014-0 to VDP), the National Science Foundation (DEB 1645137 toJGH), the Natural Sciences and Engineering Council of Canada (SJL,PPN), and the Academy of Finland (grants 257686 and 292765 toMC) for support. This work contributes to the Labex OT-Med (no.ANR-11-LABX-0061), funded by the French government throughthe A*MIDEX project (no. ANR-11-IDEX-0001-02)

Towards an applied metaecology

The complexity of ecological systems is a major challenge for practitioners and decision-makers who work to avoid, mitigate and manage environmental change. Here, we illustrate how metaecology - the study of spatial interdependencies among ecological systems through fluxes of organisms, energy, and matter - can enhance understanding and improve managing environmental change at multiple spatial scales. We present several case studies illustrating how the framework has leveraged decision-making in conservation, restoration and risk management. Nevertheless, an explicit incorporation of metaecology is still uncommon in the applied ecology literature, and in action guidelines addressing environmental change. This is unfortunate because the many facets of environmental change can be framed as modifying spatial context, connectedness and dominant regulating processes - the defining features of metaecological systems. Narrowing the gap between theory and practice will require incorporating system-specific realism in otherwise predominantly conceptual studies, as well as deliberately studying scenarios of environmental change. (C) 2019 Associacao Brasileira de Ciencia Ecologica e Conservacao. Published by Elsevier Editora Ltda.Peer reviewe

Seed Dispersal Anachronisms: Rethinking the Fruits Extinct Megafauna Ate

Background: Some neotropical, fleshy-fruited plants have fruits structurally similar to paleotropical fruits dispersed by megafauna (mammals.10 3 kg), yet these dispersers were extinct in South America 10–15 Kyr BP. Anachronic dispersal systems are best explained by interactions with extinct animals and show impaired dispersal resulting in altered seed dispersal dynamics. Methodology/Principal Findings: We introduce an operational definition of megafaunal fruits and perform a comparative analysis of 103 Neotropical fruit species fitting this dispersal mode. We define two megafaunal fruit types based on previous analyses of elephant fruits: fruits 4–10 cm in diameter with up to five large seeds, and fruits.10 cm diameter with numerous small seeds. Megafaunal fruits are well represented in unrelated families such as Sapotaceae, Fabaceae, Solanaceae, Apocynaceae, Malvaceae, Caryocaraceae, and Arecaceae and combine an overbuilt design (large fruit mass and size) with either a single or few (,3 seeds) extremely large seeds or many small seeds (usually.100 seeds). Within-family and within-genus contrasts between megafaunal and non-megafaunal groups of species indicate a marked difference in fruit diameter and fruit mass but less so for individual seed mass, with a significant trend for megafaunal fruits to have larger seeds and seediness. Conclusions/Significance: Megafaunal fruits allow plants to circumvent the trade-off between seed size and dispersal b