ArticleTheory in biosciences = Theorie in den Biowissenschaften2007
Sympatric speciation as intrinsic property of the expanding population.
Article in Theory in biosciences = Theorie in den Biowissenschaften, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Distribution of recombination hotspots in the human genome--a comparison of computer simulations with real data.PloS one · 2013Article
- Modelling survival and allele complementation in the evolution of genomes with polymorphic loci.Theory in biosciences = Theorie in den Biowissenschaften · 2011Article
- The penna model of biological aging.Bioinformatics and biology insights · 2009Article
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Authors and funding
4 authors.
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Abstract
Sympatric speciation is still debatable, though some well documented empirical data that support it already exist. Our computer modeling reveals that sympatric speciation is an intrinsic property of the expanding populations with differentiated inbreeding-higher at the edges and lower inside the territory. At the edges of expanding populations, the probability of forming deleterious phenotypes by placing two defective alleles in the corresponding loci is relatively high even with low genetic load. Thus, the winning strategy is to use rather the complementary haplotypes to form zygotes. This strategy leads to a very fast sympatric speciation and specific distribution of recombination activity along the chromosomes-higher at the subtelomeric regions (close to the ends of chromosomes) and lower in the middle of chromosomes, which is also observed in all human chromosomes (excluding Y).
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Registered trials
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