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