scispace - formally typeset
Search or ask a question
Author

Luís Borda-de-Água

Other affiliations: University of Georgia, Columbia University, University of Lisbon  ...read more
Bio: Luís Borda-de-Água is an academic researcher from University of Porto. The author has contributed to research in topics: Relative abundance distribution & Population. The author has an hindex of 17, co-authored 36 publications receiving 6168 citations. Previous affiliations of Luís Borda-de-Água include University of Georgia & Columbia University.

Papers
More filters
Book
01 Jan 2001
TL;DR: A study of the issue indicates that it is not a serious problem for neutral theory, and there is sometimes a difference between some of the simulation-based results of Hubbell and the analytical results of Volkov et al. (2003).
Abstract: study of the issue indicates that it is not a serious problem for neutral theory, for reasons we discuss below. First, a bit of background. Hubbell (2001) derived the analytical expression for the stochastic mean and variance of the abundance of a single arbitrary species in a neutral community undergoing immigration from a metacommunity source area. However, his approach did not lend itself to an analytical solution for the distribution of relative species abundance (RSA) in a multispecies community for community sizes larger than a handful of individuals. As a result, all of Hubbell's RSA distributions for local communities were based on simulations. This problem was solved by Volkov et al. (2003), who derived an analytical expression for the RSA distribution in local communities of arbitrary size. However, as Chisholm and Burgman noted, there is sometimes a difference between some of the simulation-based results of Hubbell and the analytical results of Volkov et al. (2003). Chisholm and Burgman computed Volkov's equation and resimulated Hubbell's results for the four cases

5,317 citations

Journal ArticleDOI
TL;DR: This work uses neutral theory to estimate the number, relative abundance, and range size of tree species in the Amazon metacommunity and estimate likely tree-species extinctions under published optimistic and nonoptimistic Amazon scenarios.
Abstract: New roads, agricultural projects, logging, and mining are claiming an ever greater area of once-pristine Amazonian forest. The Mil- lennium Ecosystems Assessment (MA) forecasts the extinction of a large fraction of Amazonian tree species based on projected loss of forest cover over the next several decades. How accurate are these estimates of extinction rates? We use neutral theory to estimate the number, relative abundance, and range size of tree species in the Amazon metacommunity and estimate likely tree-species ex- tinctions under published optimistic and nonoptimistic Amazon scenarios. We estimate that the Brazilian portion of the Amazon Basin has (or had) 11,210 tree species that reach sizes >10 cm DBH (stem diameter at breast height). Of these, 3,248 species have population sizes >1 million individuals, and, ignoring possible climate-change effects, almost all of these common species persist under both optimistic and nonoptimistic scenarios. At the rare end of the abundance spectrum, however, neutral theory predicts the existence of 5,308 species with <10,000 individuals each that are expected to suffer nearly a 50% extinction rate under the nonop- timistic deforestation scenario and an 37% loss rate even under the optimistic scenario. Most of these species have small range sizes and are highly vulnerable to local habitat loss. In ensembles of 100 stochastic simulations, we found mean total extinction rates of 20% and 33% of tree species in the Brazilian Amazon under the optimistic and nonoptimistic scenarios, respectively. Amazonian tree diversity neutral theory tropical tree extinction "To obtain even a very rough estimate of the total number of species in the (Amazonian) forest commu- nity, a hypothesis must be made concerning the rela- tionship between the common and rare species." Pires et al., (1)

239 citations

Journal ArticleDOI
TL;DR: It is highlighted that species abundance distributions collected at different spatial scales may collapse into a single curve after appropriate renormalization, and the power‐law form of the species‐area relationship and the Shannon, Simpson, and Berger‐Parker diversity indices belong to a family of equations relating the species number, species abundance, and area through the moments of thespecies abundance–probability density function.
Abstract: Although fractals have been applied in ecology for some time, multifractals have, in contrast, received little attention. In this article, we apply multifractals to the species-area relationship and species abundance distributions. We highlight two results: first, species abundance distributions collected at different spatial scales may collapse into a single curve after appropriate renormalization, and second, the power-law form of the species-area relationship and the Shannon, Simpson, and Berger-Parker diversity indices belong to a family of equations relating the species number, species abundance, and area through the moments of the species abundance-probability density function. Explicit formulas for these diversity indices, as a function of area, are derived. Methods to obtain the multifractal spectra from a data set are discussed, and an example is shown with data on tree and shrub species collected in a 50-ha plot on Barro Colorado Island, Panama. Finally, we discuss the implications of the multifractal formalism to the relationship between species range and abundance and the relation between the shape of the species abundance distribution and area.

83 citations

Journal ArticleDOI
Paulo A. V. Borges1, Paulo A. V. Borges2, Pedro Cardoso1, Pedro Cardoso3, Pedro Cardoso2, Holger Kreft4, Robert J. Whittaker5, Robert J. Whittaker6, Simone Fattorini2, Simone Fattorini7, Brent C. Emerson8, Artur Gil2, Rosemary G. Gillespie9, Thomas J. Matthews2, Thomas J. Matthews10, Ana M. C. Santos11, Ana M. C. Santos2, Manuel J. Steinbauer12, Christophe Thébaud13, Claudine Ah-Peng14, Isabel R. Amorim1, Isabel R. Amorim2, Silvia C. Aranda15, Ana Margarida Moura Arroz2, Ana Margarida Moura Arroz1, José M. N. Azevedo2, Mário Boieiro2, Mário Boieiro1, Luís Borda-de-Água16, José Carvalho2, José Carvalho17, Rui B. Elias2, José María Fernández-Palacios18, Margarita Florencio11, Margarita Florencio19, Margarita Florencio2, Juana María González-Mancebo18, Lawrence R. Heaney20, Joaquín Hortal8, Joaquín Hortal21, Joaquín Hortal2, Christoph Kueffer22, Benoit Lequette, José Luis Martín-Esquivel, Heriberto López8, Lucas Lamelas-Lopez2, Lucas Lamelas-Lopez1, Jose A.P. Marcelino2, Rui Nunes2, Pedro Oromí18, Jairo Patiño, Antonio José Pérez8, Carla Rego2, Carla Rego1, Sérvio P. Ribeiro2, Sérvio P. Ribeiro23, François Rigal24, François Rigal2, Pedro Rodrigues2, Pedro Rodrigues25, Andrew J. Rominger9, Margarida Santos-Reis21, Hanno Schaefer26, Cecília Sérgio21, Artur R. M. Serrano21, Manuela Sim-Sim21, P. J. Stephenson1, P. J. Stephenson22, António O. Soares2, Dominique Strasberg14, Alain Vanderporten27, Alain Vanderporten2, Virgílio Vieira1, Virgílio Vieira2, Rosalina Gabriel1, Rosalina Gabriel2 
TL;DR: The Global Island Monitoring Scheme (GIMS) as mentioned in this paper was proposed to monitor the remaining native island forests, using bryophytes, vascular plants, selected groups of arthropods and vertebrates as model taxa.
Abstract: Islands harbour evolutionary and ecologically unique biota, which are currently disproportionately threatened by a multitude of anthropogenic factors, including habitat loss, invasive species and climate change. Native forests on oceanic islands are important refugia for endemic species, many of which are rare and highly threatened. Long-term monitoring schemes for those biota and ecosystems are urgently needed: (i) to provide quantitative baselines for detecting changes within island ecosystems, (ii) to evaluate the effectiveness of conservation and management actions, and (iii) to identify general ecological patterns and processes using multiple island systems as repeated ‘natural experiments’. In this contribution, we call for a Global Island Monitoring Scheme (GIMS) for monitoring the remaining native island forests, using bryophytes, vascular plants, selected groups of arthropods and vertebrates as model taxa. As a basis for the GIMS, we also present new, optimized monitoring protocols for bryophytes and arthropods that were developed based on former standardized inventory protocols. Effective inventorying and monitoring of native island forests will require: (i) permanent plots covering diverse ecological gradients (e.g. elevation, age of terrain, anthropogenic disturbance); (ii) a multiple-taxa approach that is based on standardized and replicable protocols; (iii) a common set of indicator taxa and community properties that are indicative of native island forests’ welfare, building on, and harmonized with existing sampling and monitoring efforts; (iv) capacity building and training of local researchers, collaboration and continuous dialogue with local stakeholders; and (v) long-term commitment by funding agencies to maintain a global network of native island forest monitoring plots.

71 citations

Journal ArticleDOI
TL;DR: In this paper, the authors provided the first comprehensive global assessment of the exposure of terrestrial mammalian carnivores to roads using an integrated modelling framework and estimated critical road densities and critical patch sizes for each species based on a spatially explicit model and life-history traits.
Abstract: Aim Land-use change is a major threat to biodiversity globally. Roads cause direct mortality and limitation of individual movements, which may isolate populations and affect their viability in the long term. Here we provide the first comprehensive global assessment of the exposure of terrestrial mammalian carnivores to roads using an integrated modelling framework. Location Global. Methods We estimated critical road densities and critical patch sizes for each species based on a spatially explicit model and life-history traits. We calculated the distribution of landscape fragment sizes for each carnivore species by intersecting global road density with each species range. The proportion of a species’ geographical range with fragments below the critical patch size is used as an index of the vulnerability to roads. Results We found that the carnivores expected to be most exposed to roads belong to families Felidae, Ursidae, Mustelidae, Canidae and Procyonidae. Approximately one-third of the species most affected have not been identified by the IUCN as threatened by roads. Our model projects time to extinction that may be as low as one century for some species, such as the endangered Iberian lynx. Species are expected to be more exposed in areas with medium to high road density but, surprisingly, also in areas where road density is relatively low. Hotspots of the number of species locally endangered by roads occur in North America and Asia. Main conclusions Our results suggest the need to reassess the status and threats of those species that have not been previously recognized as strongly affected by roads. Our framework can be applied at different spatial scales, to assess the effects of the development of the road network and inform prioritization schemes for road building, and to identify areas for conservation, and species requiring particular mitigation and restoration measures.

68 citations


Cited by
More filters
Journal ArticleDOI
TL;DR: Preface to the Princeton Landmarks in Biology Edition vii Preface xi Symbols used xiii 1.
Abstract: Preface to the Princeton Landmarks in Biology Edition vii Preface xi Symbols Used xiii 1. The Importance of Islands 3 2. Area and Number of Speicies 8 3. Further Explanations of the Area-Diversity Pattern 19 4. The Strategy of Colonization 68 5. Invasibility and the Variable Niche 94 6. Stepping Stones and Biotic Exchange 123 7. Evolutionary Changes Following Colonization 145 8. Prospect 181 Glossary 185 References 193 Index 201

14,171 citations

Journal ArticleDOI
01 Jul 2004-Ecology
TL;DR: This work has developed a quantitative theory for how metabolic rate varies with body size and temperature, and predicts how metabolic theory predicts how this rate controls ecological processes at all levels of organization from individuals to the biosphere.
Abstract: Metabolism provides a basis for using first principles of physics, chemistry, and biology to link the biology of individual organisms to the ecology of populations, communities, and ecosystems. Metabolic rate, the rate at which organisms take up, transform, and expend energy and materials, is the most fundamental biological rate. We have developed a quantitative theory for how metabolic rate varies with body size and temperature. Metabolic theory predicts how metabolic rate, by setting the rates of resource uptake from the environment and resource allocation to survival, growth, and reproduction, controls ecological processes at all levels of organization from individuals to the biosphere. Examples include: (1) life history attributes, including devel- opment rate, mortality rate, age at maturity, life span, and population growth rate; (2) population interactions, including carrying capacity, rates of competition and predation, and patterns of species diversity; and (3) ecosystem processes, including rates of biomass production and respiration and patterns of trophic dynamics. Data compiled from the ecological literature strongly support the theoretical predictions. Even- tually, metabolic theory may provide a conceptual foundation for much of ecology, just as genetic theory provides a foundation for much of evolutionary biology.

6,017 citations

Journal ArticleDOI
TL;DR: This framework is used to discuss why the metacommunity concept is useful in modifying existing ecological thinking and illustrate this with a number of both theoretical and empirical examples.
Abstract: The metacommunity concept is an important way to think about linkages between different spatial scales in ecology. Here we review current understanding about this concept. We first investigate issues related to its definition as a set of local communities that are linked by dispersal of multiple potentially interacting species. We then identify four paradigms for metacommunities: the patch-dynamic view, the species-sorting view, the mass effects view and the neutral view, that each emphasizes different processes of potential importance in metacommunities. These have somewhat distinct intellectual histories and we discuss elements related to their potential future synthesis. We then use this framework to discuss why the concept is useful in modifying existing ecological thinking and illustrate this with a number of both theoretical and empirical examples. As ecologists strive to understand increasingly complex mechanisms and strive to work across multiple scales of spatio-temporal organization, concepts like the metacommunity can provide important insights that frequently contrast with those that would be obtained with more conventional approaches based on local communities alone.

4,266 citations

Journal ArticleDOI
TL;DR: A common pattern of phylogenetic conservatism in ecological character is recognized and the challenges of using phylogenies of partial lineages are highlighted and phylogenetic approaches to three emergent properties of communities: species diversity, relative abundance distributions, and range sizes are reviewed.
Abstract: ▪ Abstract As better phylogenetic hypotheses become available for many groups of organisms, studies in community ecology can be informed by knowledge of the evolutionary relationships among coexisting species. We note three primary approaches to integrating phylogenetic information into studies of community organization: 1. examining the phylogenetic structure of community assemblages, 2. exploring the phylogenetic basis of community niche structure, and 3. adding a community context to studies of trait evolution and biogeography. We recognize a common pattern of phylogenetic conservatism in ecological character and highlight the challenges of using phylogenies of partial lineages. We also review phylogenetic approaches to three emergent properties of communities: species diversity, relative abundance distributions, and range sizes. Methodological advances in phylogenetic supertree construction, character reconstruction, null models for community assembly and character evolution, and metrics of community ...

3,615 citations

Journal ArticleDOI
TL;DR: Current evidence confirms that, as proposed by the Baas-Becking hypothesis, 'the environment selects' and is, in part, responsible for spatial variation in microbial diversity, but recent studies also dispute the idea that 'everything is everywhere'.
Abstract: We review the biogeography of microorganisms in light of the biogeography of macroorganisms A large body of research supports the idea that free-living microbial taxa exhibit biogeographic patterns Current evidence confirms that, as proposed by the Baas-Becking hypothesis, 'the environment selects' and is, in part, responsible for spatial variation in microbial diversity However, recent studies also dispute the idea that 'everything is everywhere' We also consider how the processes that generate and maintain biogeographic patterns in macroorganisms could operate in the microbial world

2,456 citations