Institution
Konrad Lorenz Institute for Evolution and Cognition Research
Other•Klosterneuburg, Austria•
About: Konrad Lorenz Institute for Evolution and Cognition Research is a other organization based out in Klosterneuburg, Austria. It is known for research contribution in the topics: Philosophy of biology & Population. The organization has 105 authors who have published 282 publications receiving 10639 citations. The organization is also known as: KLI.
Papers published on a yearly basis
Papers
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TL;DR: The powerful visualization tools of geometric morphometrics and the typically large amount of shape variables give rise to a specific exploratory style of analysis, allowing the identification and quantification of previously unknown shape features.
Abstract: Geometric morphometrics is the statistical analysis of form based on Cartesian landmark coordinates. After separating shape from overall size, position, and orientation of the landmark configurations, the resulting Procrustes shape coordinates can be used for statistical analysis. Kendall shape space, the mathematical space induced by the shape coordinates, is a metric space that can be approximated locally by a Euclidean tangent space. Thus, notions of distance (similarity) between shapes or of the length and direction of developmental and evolutionary trajectories can be meaningfully assessed in this space. Results of statistical techniques that preserve these convenient properties—such as principal component analysis, multivariate regression, or partial least squares analysis—can be visualized as actual shapes or shape deformations. The Procrustes distance between a shape and its relabeled reflection is a measure of bilateral asymmetry. Shape space can be extended to form space by augmenting the shape coordinates with the natural logarithm of Centroid Size, a measure of size in geometric morphometrics that is uncorrelated with shape for small isotropic landmark variation. The thin-plate spline interpolation function is the standard tool to compute deformation grids and 3D visualizations. It is also central to the estimation of missing landmarks and to the semilandmark algorithm, which permits to include outlines and surfaces in geometric morphometric analysis. The powerful visualization tools of geometric morphometrics and the typically large amount of shape variables give rise to a specific exploratory style of analysis, allowing the identification and quantification of previously unknown shape features.
1,017 citations
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Memorial Sloan Kettering Cancer Center1, Bilkent University2, SRI International3, Université libre de Bruxelles4, Ontario Institute for Cancer Research5, New York University6, National Institutes of Health7, National Autonomous University of Mexico8, Boston University9, Cold Spring Harbor Laboratory10, Johns Hopkins University11, University of Toronto12, Rothamsted Research13, University of Rennes14, Cell Signaling Technology15, Broad Institute16, Food and Drug Administration17, Virginia Tech18, Oregon Health & Science University19, United States Environmental Protection Agency20, Argonne National Laboratory21, University of Connecticut22, Harvard University23, National Institute of Standards and Technology24, University of Cambridge25, National University of Ireland, Galway26, Konrad Lorenz Institute for Evolution and Cognition Research27, Maastricht University28, University of Auckland29, Syngenta30, Stanford University31, Yale University32, Loyola Marymount University33, St. John's University34, Columbia University35, SRA International36, Novartis37, University of Ottawa38, Vertex Pharmaceuticals39, Medical College of Wisconsin40, Gladstone Institutes41, Cornell University42, Takeda Pharmaceutical Company43, University of Chicago44, Total S.A.45, Kyoto University46, California Institute of Technology47
TL;DR: Thousands of interactions, organized into thousands of pathways, from many organisms are available from a growing number of databases, and this large amount of pathway data in a computable form will support visualization, analysis and biological discovery.
Abstract: Biological Pathway Exchange (BioPAX) is a standard language to represent biological pathways at the molecular and cellular level and to facilitate the exchange of pathway data. The rapid growth of the volume of pathway data has spurred the development of databases and computational tools to aid interpretation; however, use of these data is hampered by the current fragmentation of pathway information across many databases with incompatible formats. BioPAX, which was created through a community process, solves this problem by making pathway data substantially easier to collect, index, interpret and share. BioPAX can represent metabolic and signaling pathways, molecular and genetic interactions and gene regulation networks. Using BioPAX, millions of interactions, organized into thousands of pathways, from many organisms are available from a growing number of databases. This large amount of pathway data in a computable form will support visualization, analysis and biological discovery.
673 citations
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TL;DR: The aim of the ecospat package is to make available novel tools and methods to support spatial analyses and modeling of species niches and distributions in a coherent workflow and stimulate the use of comprehensive approaches in spatial modelling of species and community distributions.
Abstract: The aim of the ecospat package is to make available novel tools and methods to support spatial analyses and modeling of species niches and distributions in a coherent workflow. The package is written in the R language (R Development Core Team 2016) and contains several features, unique in their implementation, that are complementary to other existing R packages. Pre-modeling analyses include species niche quantifications and comparisons between distinct ranges or time periods, measures of phylogenetic diversity, and other data exploration functionalities (e.g. extrapolation detection, ExDet). Core modeling brings together the new approach of Ensemble of Small Models (ESM) and various implementations of the spatially-explicit modeling of species assemblages (SESAM) framework. Post-modeling analyses include evaluation of species predictions based on presence-only data (Boyce index) and of community predictions, phylogenetic diversity and environmentally-constrained species co-occurrences analyses. The ecospat package also provides some functions to supplement the biomod2 package (e.g. data preparation, permutation tests and cross-validation of model predictive power). With this novel package, we intend to stimulate the use of comprehensive approaches in spatial modelling of species and community distributions.
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618 citations
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TL;DR: This essay identifies major theoretical themes of current evo–devo research and highlights how its results take evolutionary theory beyond the boundaries of the Modern Synthesis.
Abstract: Evolutionary developmental biology (evo-devo) explores the mechanistic relationships between the processes of individual development and phenotypic change during evolution. Although evo-devo is widely acknowledged to be revolutionizing our understanding of how the development of organisms has evolved, its substantial implications for the theoretical basis of evolution are often overlooked. This essay identifies major theoretical themes of current evo-devo research and highlights how its results take evolutionary theory beyond the boundaries of the Modern Synthesis.
499 citations
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TL;DR: A general methodological framework by which missing information about biological specimens can be estimated using geometric morphometric methods is outlined and how this relates to effective paleoanthropological use of incomplete and distorted crania is discussed.
376 citations
Authors
Showing all 107 results
Name | H-index | Papers | Citations |
---|---|---|---|
Fred L. Bookstein | 94 | 382 | 45669 |
Antoine Guisan | 85 | 332 | 55475 |
Nicolas Salamin | 50 | 180 | 9178 |
Thomas Bugnyar | 45 | 152 | 5652 |
Christophe F. Randin | 42 | 75 | 8837 |
D. Kimbrough Oller | 42 | 152 | 8152 |
Philipp Mitteroecker | 36 | 101 | 6655 |
Gerd B. Müller | 36 | 92 | 6170 |
Johannes Jaeger | 35 | 76 | 3831 |
Olivier Broennimann | 34 | 70 | 8604 |
Joanna J. Bryson | 31 | 175 | 4654 |
Judith M. Burkart | 30 | 91 | 4201 |
Luca Tommasi | 29 | 133 | 3004 |
Mihaela Pavlicev | 28 | 75 | 3647 |
Zsófia Virányi | 26 | 56 | 3636 |