PHILOSOPHICAL POSTURE
Iver Leandro Daza
Traditionally the objective of parsimony has been reduced to the expression of William de Ockham: "it is useless to do with more what can be done with less", and this in essence has been said to be the principle of parsimony [1]. Parsimony, among other principles for inference, have been proposed to reach conclusions about phylogenetic relationships [2]. Maximum parsimony (MP), seeks to find the tree topology that requires the least amount of changes in the state of the character to produce the characteristics of the terminals present in the tree and build said phylogenetic relationships and, additionally, provides an ordering of the trees produced from "best" to “worst” [3]. This inference method requires that the researcher distinguish between antetral and derived characters, plesiomorphies of apomorphies, in the data set to be used [4]. With this said, the best genealogy is the one that contains the least homoplasy [2].
Among the main arguments against the use
of parsimony, it is found that parsimony implicitly assumes doubtful
propositions about evolutionary processes [3]. For authors who propose against the use of
parsimony, such as Felsenstein, this may be inconsistent under a simplified
process model and also consider that in empirical data it has a higher
probability of failure [5]. Another argument mentions that it tries to
estimate too many parameters, this comes from the fact that, if each character
of the data is allowed its own branch length vector, the parsimony results are
similar to Maximum likelihood [6]. Parsons also argues against it, mentioning that
the simplest explanation is not always correct, and there is no prima facie
reason to believe that a theory is correct because of the number of objects or
entities it contains [7].
Despite the opposition against this approach,
there are others who favor this perspective. Platnick and Gaffne in a discussion of Popper and systematics suggested
that the best method for phylogenetic inferences is the one on which strong
proofs can be developed in the Popperian sense, which could offer a
justification for the use of cladistic parsimony [8]. In fact, Sober maintains that phylogenetic
reconstructions are better interpreted from the Popperian corroboration [5]. Even when it’s generally accepted that for molecular analyzes likelihood is
more appropriate, as well as inference by parsimony is more appropriate for
morphological data, it has not been proven and in fact it is more “a social
fact and not something logically inevitable", in other words, the data
does not have an explicit indicator of which method is better for the analysis [3]
It seems the homoplasy interference while
trying to study the phylogenetic relationship in the clade caudata has not been
fully resolved using these approaches, that’s why the implied weighing method
of the MP has a certain appeal given the fact that no other research (not even
the amphibian tree of life phylogeny [9]) has tried to reweight characters
given the rampant homoplasy some authors claim have found [10,11]. The justification for the use of
parsimony is quite dependent on philosophical and statistical inference [1] just as corroboration and
probability both are linked, as discussed by popper [8]. In the maximum parsimony the
implied weighing method follows the inverse ratio path that the corroboration
and probability have, as the more homoplasy found in a tree’s character, the
less impact it has on the subsequent construction of the trees.
The ongoing debate on which method might be
better will continue, but I am not going to say that future works using
Bayesian inference or maximum likelihood methods will not be helpful. The
current approach is a proposal to resolve the current situation and try to
emphasize the important of parsimony method among the family-level relationship
of the salamanders
Bibliography
1.Sober E. 2004 The contest between
parsimony and likelihood. Syst. Biol. 53, 644–653.
2.Rodríguez
A et al. 2017 Inferring the shallow phylogeny of true salamanders
(Salamandra) by multiple phylogenomic approaches. Mol. Phylogenet. Evol.
115, 16–26.
3.Coelho
MTP, Diniz-Filho JA, Rangel TF. 2019 A parsimonious view of the parsimony
principle in ecology and evolution. Ecography (Cop.). 42,
968–976.
4.Sober
E. 1983 Parsimony in Systematics. Ann. Rev. Ecol. Syst. 14,
335–357.
5.Popper
K. 2005 The logic of scientific discovery. Routledge.
6.Daniel
F, Peter C. 2016 Probability , Parsimony , and Popper . Cranston Published by :
Oxford University Press for the Society of Systematic Biologists Stable Pa. Syst.
Biol. 41, 252–257.
No hay comentarios:
Publicar un comentario