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Showing papers in "Biodiversity Informatics in 2020"


Journal ArticleDOI
TL;DR: In this article, the authors provide a manual with the basic routines used in this field and a practical example of its implementation to promote good practices and guidance for new users, as well as a good example of how to use them.
Abstract: Ecological niche modeling (ENM) and species distribution modeling (SDM) are sets of tools that allow the estimation of distributional areas on the basis of establishing relationships among known occurrences and environmental variables. These tools have a wide range of applications, particularly in biogeography, macroecology, and conservation biology, granting prediction of species potential distributional patterns in the present and dynamics of these areas in different periods or scenarios. Due to their relevance and practical applications, the usage of these methodologies has significantly increased throughout the years. Here, we provide a manual with the basic routines used in this field and a practical example of its implementation to promote good practices and guidance for new users.

31 citations


Journal ArticleDOI
TL;DR: In this paper, point location records for 226 anonymised species from six regions of the world, with accompanying predictor variables in raster (grid) and point formats, are published as a benchmark for modeling approaches and for testing new ways to evaluate the accuracy of SDMs.
Abstract: Species distribution models (SDMs) are widely used to predict and study distributions of species. Many different modeling methods and associated algorithms are used and continue to emerge. It is important to understand how different approaches perform, particularly when applied to species occurrence records that were not gathered in structured surveys (e.g. opportunistic records). This need motivated a large-scale, collaborative effort, published in 2006, that aimed to create objective comparisons of algorithm performance. As a benchmark, and to facilitate future comparisons of approaches, here we publish that dataset: point location records for 226 anonymised species from six regions of the world, with accompanying predictor variables in raster (grid) and point formats. A particularly interesting characteristic of this dataset is that independent presence-absence survey data are available for evaluation alongside the presence-only species occurrence data intended for modeling. The dataset is available on Open Science Framework and as an R package and can be used as a benchmark for modeling approaches and for testing new ways to evaluate the accuracy of SDMs.

29 citations


Journal ArticleDOI
TL;DR: This work assesses a body of work that has attempted to use co-occurrence networks to infer the existence and type of biotic interactions between species and examines a series of examples that demonstrates striking discords between interactions inferred from co-Occurrence patterns and previous experimental results and known life-history details.
Abstract: We assess a body of work that has attempted to use co-occurrence networks to infer the existence and type of biotic interactions between species. Although we see considerable interest in the approach as an exploratory tool for understanding patterns of co-occurrence of species, we note and describe numerous problems in the step of inferring biotic interactions from the co-occurrence patterns. These problems are both theoretical and empirical in nature, and limit confidence in inferences about interactions rather severely. We examine a series of examples that demonstrates striking discords between interactions inferred from co-occurrence patterns and previous experimental results and known life-history details.

18 citations


Journal ArticleDOI
TL;DR: The abundant niche centroid hypothesis as discussed by the authors is a popular alternative to the abundance-distance-to-niche hypothesis. But it has been shown that for some species, when the environmental equilibrium condition is violated, it is impossible to accurately characterize their true niche.
Abstract: Correlative estimates of fundamental niches are gaining momentum as an alternative to predict species’ abundances, particularly via the abundant niche-centroid hypothesis (an expected inverse relationship between species’ abundance variation across its range and the distance to the geometric centroid of its multidimensional ecological niche). The main goal of this review is to recapitulate what has been done, where we are now, and where should we move towards in regards to this hypothesis. Despite evidence in support of the abundance-distance to niche centroid relationship, its usefulness has been highly debated, although with little consideration of the underlying theory regarding the circumstances that might break down the relationship. We address some key points about the conditions needed to test the hypothesis in correlative studies, specifically in relation to nichecharacterization and configurations of the Biotic-Abiotic-Mobility (BAM) framework to illustrate the problem of unfilled niches. Using a created supraspecific modeling unit, we show that species for which only a portion of their fundamental niche is represented in their area of historical accessibility (M)—i.e., when the environmental equilibrium condition is violated—it is impossible to characterize their true niche centroid. Therefore, we strongly recommend to analyze this assumption prior toassess the abundant niche-centroid hypothesis. Finally, we discuss the potential of using modeling units above the species level for cases in which environmental conditions associated with species’ occurrences may not be sufficient to fully characterize their fundamental niches.

16 citations


Journal ArticleDOI
TL;DR: In this paper, the authors provide a joint review of the submissions by Stephens et al. and Peterson et al., and suggest that spatiotemporal data, when available, is a much more powerful tool for discerning interactions than do staticspatial data.
Abstract: Dr. Luis Escobar asked me to provide a joint review of the submissions by Stephens et al. (2019, this issue) and Peterson et al. (2019, this issue). I pulled thoughts together, but by the time I sent them along, he had received other reviews and made an editorial decision. He felt my perspective might nevertheless warrant publishing as a commentary alongside these two pieces. My review was of the original submissions, which are now appearing with minor, mainly cosmetic changes. I have only lightly edited the text of my review, and added a few additional thoughts and pertinent references. Neither group of authors has seen my commentary, and so I am responsible for any omissions or lapses in interpretation. The protocol developed by Stephens seems to me a potentially valuable exploratory tool in describing patterns of co-occurrence, but I note several potential problems in identifying interactions usingsolely this protocol. I also gently disagree with Peterson et al., who state flatly that co-occurrence data can shed no light at all on interspecific interactions. I suggest there are a number of counter-examples to this claim in the literature. I argue that spatiotemporal data, when available, iprovide a much more powerful tool for discerning interactions, than do staticspatial data. Finally, I use a simple thought experiment to point out that biotic drivers could be playing a key causal role in limitnig distributions, even in equisitlvely accurate SDMs that use only abiotic (scenopoetic) data as input data.

9 citations


Journal ArticleDOI
TL;DR: The abundant-center hypothesis as mentioned in this paper posits that species density should be highest in the center of the geographic range or climatic niche of a species, based on the idea that the centre of either will be the area with the highest demographic performance (e.g., greater fecundity, survival or carrying capacity).
Abstract: The abundant-center hypothesis posits that species density should be highest in the center of the geographic range or climatic niche of a species, based on the idea that the center of either will be the area with the highest demographic performance (e.g., greater fecundity, survival, or carrying capacity). While intuitive, current support for the hypothesis is quite mixed. Here, we discuss the current state of the abundant-center hypothesis, highlighting the relatively low level of support for the relationship. We then discuss the potential reasons for this lack of empirical support, emphasizing the inherent ecological complexity which may prevent the observation of the abundant-center in natural systems. This includes the role of non-equilibrial population dynamics, species interactions, landscape structure, and dispersal processes, as well as variable data quality and inconsistent methodology. The incorporation of this complexity into studies of the distribution of species densities in geographic or niche space may underlie the limited empirical support for the abundant-center hypothesis. We end by discussing potentially fruitful research avenues. Most notably, we highlight the need for theoretical development and controlled experimental testing of the abundant-center hypothesis.

7 citations


Journal ArticleDOI
TL;DR: An overview of a Bayesian inference framework, developed over the last 10 years, which, using spatial data, offers a general formalism within which ecological interactions may be characterised and quantied, and which can be used to quantify confounding and therefore help disentangle the complex causal chains that are present in ecosystems.
Abstract: The characterisation and quantication of ecological interactions, and the construction of species distributions and their associated ecological niches, is of fundamental theoretical and practical importance. In this paper we give an overview of a Bayesian inference framework, developed over the last 10 years, which, using spatial data, offers a general formalism within which ecological interactions may be characterised and quantied. Interactions are identied through deviations of the spatial distribution of co-occurrences of spatial variables relative to a benchmark for the non-interacting system, and based on a statistical ensemble of spatial cells. The formalism allows for the integration of both biotic and abiotic factors of arbitrary resolution. We concentrate on the conceptual and mathematical underpinnings of the formalism, showing how, using the Naive Bayes approximation, it can be used to not only compare and contrast the relative contribution from each variable, but also to construct species distributions and niches based on arbitrary variable type. We show how the formalism can be used to quantify confounding and therefore help disentangle the complex causal chains that are present in ecosystems. We also show species distributions and their associated niches can be used to infer standard "micro" ecological interactions, such as predation and parasitism. We present several representative use cases that validate our framework, both in terms of being consistent with present knowledge of a set of known interactions, as well as making and validating predictions about new, previously unknown interactions in the case of zoonoses.

6 citations


Journal ArticleDOI
TL;DR: For instance, Stephens et al. as mentioned in this paper proposed a method to detect the presence of cancer in the human brain using the results of the Centro de Ciencias de la Complejidad (C3) of the Universidad Nacional Autónoma de México (Unidad Lerma).
Abstract: Christopher R. Stephens1, 2, Constantino González-Salazar1, 3, María del Carmen Villalobos-Segura4 and Pablo A. Marquet1, 5 1C3 Centro de Ciencias de la Complejidad, Universidad Nacional Autónoma de México, Mexico City, Mexico. 2Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Mexico City, Mexico; stephens@nucleares.unam.mx. 3Departamento de Ciencias Ambientales, CBS Universidad Autónoma Metropolitana, Unidad Lerma; Estado de México, Mexico; cgsalazar7@gmail.com. 4Laboratorio Ecología de Enfermedades y Una Salud, Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autónoma de México, Mexico City, Mexico. 5Departamento de Ecología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile; Instituto de Ecología y Biodiversidad (IEB), Santiago, Chile and The Santa Fe Institute, 1399 Hyde Park Road, Santa Fe, NM 8731, USA.

4 citations