Principios de Taxonomia
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42j 2 Why is there a Species Problem?<br />
populations that would double or triple today s internationally agreed upon number<br />
of approximately 9000 bird species.<br />
The situation is the same with regard to <strong>de</strong>scent relations or kinship. Monophyletic,<br />
apomorphy-based bifurcations can be traced by mo<strong>de</strong>rn molecular technology<br />
into the minutest branches, and in doing so, these traces can be justified in a<br />
theoretically consistent manner to represent speciation according to the cladistic<br />
species concept. There are always some autapomorphies if two sister individuals are<br />
born by the parents (Chapter 7). In the exploration of the cladistic bifurcations in the<br />
genealogical tree, branching into repeatedly new lateral branches can lead to an<br />
inscrutable chaos of cla<strong>de</strong>s. One branch follows the other and the branches are<br />
continually inter-nested (Mishler, 1999). This may increase the species numbers<br />
currently in use by a 100-fold (Cracraft, 1997; Mallet, 1995). Where does one begin to<br />
assign organisms to species, and where does one stop?<br />
A similar situation arises with regard to species as gene-flow communities<br />
(Chapter 6). Tiny, isolated, reproductively separated populations can disaggregate<br />
into hundreds or thousands of groups of organisms that no longer have gene flow<br />
among themselves. These <strong>de</strong>limited gene-flow communities can be small if the<br />
organisms are not very mobile and if numerous barriers splinter the totality of<br />
organisms into the smallest separated gene-flow communities. Consi<strong>de</strong>ring each<br />
isolated gene-flow community as a separate species also could increase the species<br />
number currently in use by a 100-fold.<br />
What is the consequence of this dilemma? From this dilemma it follows that there<br />
are, and probably always must be, two different taxonomies (Schmitt, 2004).<br />
Biodiversity can be sorted into manageable units with which humans pursue goals<br />
and achieve results that satisfy practical needs, but nothing more. The second<br />
taxonomy is based on the theory of evolution. Descent and kinship play a role, as<br />
do reproductive communities. This is a taxonomy that does not follow operational<br />
convenience, but it satisfies the human need for consistency in lines of thinking.<br />
The species problem as a never-ending story does not seem to stem from the<br />
disagreement about the more than twenty species concepts currently on the market<br />
(May<strong>de</strong>n, 1997), ranging from the phenetic species concept and the concept of the<br />
reproductive community to the ecological species concept. This abundance of species<br />
concepts is usually called species pluralism (Hull, 1999). Instead, the species<br />
problem seems to hearken back to the fundamental difference between the theoretical<br />
concept of and the practical instructions for how to distinguish different<br />
species (Ereshefsky, 1999).<br />
It may be unavoidable to separate both taxonomies from the start. Both<br />
taxonomies pursue different goals. One taxonomy conducts a classification that<br />
is feasible and serves for communication between scientists and laypeople. The<br />
other taxonomy is concerned with the biological unit that plays a role in evolution<br />
and is subject to natural selection for this reason. The question is to what extent<br />
nature has an interest in organizing organisms into cohesive groups that are<br />
maintained as isolated groups without merging into others. This kind of a natural<br />
species is a unit in biodiversity that would be present without human-imposed<br />
principles of or<strong>de</strong>r.