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1.
Proc Natl Acad Sci U S A ; 114(51): E10937-E10946, 2017 12 19.
Article in English | MEDLINE | ID: mdl-29196525

ABSTRACT

Our ability to understand and predict the response of ecosystems to a changing environment depends on quantifying vegetation functional diversity. However, representing this diversity at the global scale is challenging. Typically, in Earth system models, characterization of plant diversity has been limited to grouping related species into plant functional types (PFTs), with all trait variation in a PFT collapsed into a single mean value that is applied globally. Using the largest global plant trait database and state of the art Bayesian modeling, we created fine-grained global maps of plant trait distributions that can be applied to Earth system models. Focusing on a set of plant traits closely coupled to photosynthesis and foliar respiration-specific leaf area (SLA) and dry mass-based concentrations of leaf nitrogen ([Formula: see text]) and phosphorus ([Formula: see text]), we characterize how traits vary within and among over 50,000 [Formula: see text]-km cells across the entire vegetated land surface. We do this in several ways-without defining the PFT of each grid cell and using 4 or 14 PFTs; each model's predictions are evaluated against out-of-sample data. This endeavor advances prior trait mapping by generating global maps that preserve variability across scales by using modern Bayesian spatial statistical modeling in combination with a database over three times larger than that in previous analyses. Our maps reveal that the most diverse grid cells possess trait variability close to the range of global PFT means.


Subject(s)
Ecosystem , Plants , Quantitative Trait, Heritable , Environment , Geography , Models, Statistical , Plant Dispersal , Spatial Analysis
2.
Bioinformatics ; 27(3): 295-302, 2011 Feb 01.
Article in English | MEDLINE | ID: mdl-21115437

ABSTRACT

MOTIVATION: High-throughput sequencing technologies produce very large amounts of data and sequencing errors constitute one of the major problems in analyzing such data. Current algorithms for correcting these errors are not very accurate and do not automatically adapt to the given data. RESULTS: We present HiTEC, an algorithm that provides a highly accurate, robust and fully automated method to correct reads produced by high-throughput sequencing methods. Our approach provides significantly higher accuracy than previous methods. It is time and space efficient and works very well for all read lengths, genome sizes and coverage levels. AVAILABILITY: The source code of HiTEC is freely available at www.csd.uwo.ca/~ilie/HiTEC/.


Subject(s)
Algorithms , Sequence Analysis, DNA/methods , Genome , Models, Genetic , Reproducibility of Results , Software
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