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Principios de Taxonomia

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138j 6 Biological Species as a Gene-Flow Community<br />

6.7<br />

Why do the Individuals of a Species Resemble Each Other?<br />

Why do the organisms of a species resemble each other? There are three possible<br />

ways to explain this.<br />

1) First, resemblance can be the result of a common <strong>de</strong>scent. Children resemble<br />

their parents because of <strong>de</strong>scent; however, mutation and selection cause increasing<br />

alteration of traits. As a consequence, genetic and phenotypic heterogeneity<br />

grow over time. Finally, over long evolutionary stretches, the more or less<br />

homogeneous appearance of the individuals of a species can no longer be<br />

explained by their common <strong>de</strong>scent.<br />

2) Secondly, the homogeneous appearance of the organisms of a species may result<br />

from a repeated stabilizing of the genomes via sexual genome fusion. Thus,<br />

continuing biparental sexual contacts between organisms prevent genomic<br />

divergence. If a group of organisms at the periphery of the distribution area of<br />

the species were to adapt to local environmental conditions, these divergent<br />

<strong>de</strong>velopments would be reversed by backcrossing with the organisms living at the<br />

center of the distribution area. How strong are these forces? How often and across<br />

which distances are the genomes of distant organisms stabilized by sperm-egg<br />

fusion and genetic recombination? Can newly mutated alleles really reach all<br />

distant areas of the species range? Does the well-known phenomenon of allele<br />

fixation really reach all distant populations of a species?<br />

The cofoun<strong>de</strong>rs of the gene-flow-community species concept, Theodosius<br />

Dobzhansky and Ernst Mayr, put substantial weight on the homogenizing force<br />

of genetic recombination. In sexual gene flow, they saw a main reason why species<br />

actually exist (see the Section The why of speciation in Mayr, 2000). The 1930s<br />

and 1940s were the time of the Great Synthesis, which was a joining of<br />

evolution, genetics and taxonomy. Gene flow among the organisms of a geneflow<br />

community was not only perceived as a connecting force that keeps the<br />

individuals of a species together, but also as the cause of the organisms i<strong>de</strong>ntity of<br />

traits across the entire range of the species. Gene flow was thought to cause the<br />

organisms in a community to have an overall homogeneous appearance and<br />

thus belong to the same species (Dobzhansky, 1937; Mayr, 1942). The morphological<br />

and physiological integrity of a species was thought to be created and<br />

maintained by gene flow.<br />

The reasoning behind this was as follows: because of local adaptations in<br />

different regions, the subpopulations in the long run would follow separate<br />

evolutionary pathways and thus would become increasingly divergent. Backcrossing,<br />

however, would occur repeatedly. Consequently, genomic interchange<br />

among the distant organisms would result in homogeneity of the genotypes.<br />

Because of genetic recombination, in principle, all allelic variants would reach all<br />

of the genomes in a population of a species. If some organisms were to diverge by<br />

mutation and selection, these <strong>de</strong>viations would again be reversed. Biparental<br />

sexuality would hin<strong>de</strong>r this divergence among the organisms of a gene-flow

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