Principios de Taxonomia
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84j 4 What are Traits in Taxonomy?<br />
In contrast, the same or similar <strong>de</strong>velopmental processes in different taxa can be<br />
controlled by markedly different genes that are non-homologous to each other. For<br />
example, gastrulation in the early embryonic <strong>de</strong>velopment is referred to as homologous<br />
across all vertebrates, although this <strong>de</strong>velopmental process is controlled by<br />
significantly different genetic mechanisms. Thus, it is not consistent to label the<br />
gastrulae of different animal phyla as homologous. This constraint is at best present<br />
for some of the partial components that are involved in gastrulation. Only these<br />
components can be consi<strong>de</strong>red to be homologous. Another example are the supposedly<br />
homologous body segments of Drosophila and of the Migratory Locust<br />
(Locusta), which are, however, genetically controlled by different transcription<br />
factors. Thus, these body segments, as a whole, cannot be homologous to each<br />
other, because only some components are homologous. Similarly, one would not<br />
label two things as being colored red when they are colored both red and blue, so that<br />
the commonness of both is not only the color red.<br />
Furthermore, the concept of homology becomes less and less useful in its<br />
significance and meaning when going further back into phylogeny. If two structures<br />
<strong>de</strong>scend from a common ancestor that traces far back into phylogeny, then the<br />
assessment of the common <strong>de</strong>scent and, thus, the prevailing homology relation does<br />
not produce any specific gain in scientific knowledge, although it is logically<br />
unassailable to call all of these structures homologous. Because of the common<br />
<strong>de</strong>scent of all of life, every structure is, in the end, homologous to every other<br />
structure.<br />
4.9<br />
The Vertebrate Eye and the Squid Eye: They Cannot be Homologous Nor can they<br />
be Non-Homologous<br />
Most traits are complex. This observation means that what is consi<strong>de</strong>red by the<br />
taxonomist to be a trait in reality is a complex structure that is composed of several<br />
components, because evolution has structured the traits of a phenotype according<br />
to a modular principle. The individual components of a single trait sometimes<br />
share very different evolutionary histories. This scenario clearly means that many<br />
traits cannot be homologous and also not non-homologous, because they are<br />
composed of components with different phylogenetic <strong>de</strong>scents. Even several<br />
proteins can be partially homologous to each other and partially not homologous,<br />
because different proteins can be modularly assembled from different domains. If<br />
two proteins in two different organisms are compared, some of the domains of a<br />
specific protein might be homologous, whereas other domains of the same protein<br />
might be convergent parts that have in<strong>de</strong>pen<strong>de</strong>nt evolutionary origins. Examples of<br />
this phenomenon are some trans-membrane domains and specific receptor<br />
domains (Ast, 2005).<br />
The concept of homology is often misun<strong>de</strong>rstood. The disagreement of scientists<br />
on the concept s formation has led to the homology problem (Bock, 1989).<br />
Researchers with differing interests, experiences and objectives have <strong>de</strong>fined the