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Why Alpha Taxonomy is Better than
Phylogenetics Richard H. Zander April 3, 2012 |
Why Alpha Taxonomy is Better than Phylogenetics Richard H.
Zander, Alpha taxonomy and cladistics both attempt the devising of
hypotheses about groups of organisms in nature. The hypotheses must be
testable, relevant, preferably bold in the Popperian sense, and explanatory.
There should be as few as possible that are supported by the same data. The
simplest or most easily refutable can be tested first to minimize time and
labor. Abduction, as opposed to induction or deduction, is the process of
creating testable hypotheses, usually through educated guesswork or a system
of rules. A most impressive example of abduction is that of physicist Edward
Tryon (Parker 1988: 190) who realized that the universe’s gravitational
potential energy was exactly that of its mass energy, but negative, thus the
net energy of the universe was zero. Thus, probabilistic vacuum quantum pair
fluctuation could well have been the origin of the universe. A neat
hypothesis like this is based on expertise and hundreds of years of standing
on the shoulders of giants. The “creative act” associated with intuition is well discussed by
Springer and Deutsch (1993: 312), who give examples of major scientific
discoveries associated with hypnagogic semi-dream states. Such eureka events,
however, are cited as not “accidental or purely intuitive discovery.” Most
are in a scientific context associated with a long term problem, with a
background “set by years of rigorous work,” often with a latent period in
which, apparently, the unconscious attends to the puzzle. Alpha taxonomy has, in fact, this same background for its
hypotheses, even the grounding in physics. A recent study (Zander, in
preparation3) found that the metric dimensional paradigm in descriptions
where a usual range of measurements is given along with ranges for extreme
low and extreme high measurements in the form (low-)usual(-high), or
(a–)b–c(–d). Analysis of actual measurements for several alpha taxonomic
treatments of mosses showed that the ideal range proportion was represented by
a Fibonacci series in powers of the golden ratio, or 1:1.62:1.6,
or 1:2.6:1.6. (Where 1.6 is
approximately the golden ratio.) The geometric mean of the usual range was
the same as the geometric mean of the full range including the extremes,
which is expected statistically for ranges that cross most of a magnitude or
with are a large proportion of the range from zero to the greatest extreme. Alpha taxonomy is particularly good at identifying conservative
expressed traits that are operative in signaling relationships in small or
large groups, and in weighting traits according to their covariant value in
discerning groups explainable by macroevolutionary transformations. Morphological cladistics is good at creating branching trees by
organizing complex data, but (1) usually weights all data the same, thus
rejecting the special value of conservative traits as tracking evolution, and
(2) globalizes traits, including the conservative, such that traits that do
signal relationship in one group are necessarily forced to track
relationships in another in which they may not be conservative. The best one
can do is split the data sets into small groups, weight the data, and try to
construct a natural key with more precision and detail than one could do
without software. Molecular analysis ignores the possibility of unsampled paraphyly
and extended paraphyly by representing at least species and genera by one or
few sampled specimens. Thus resolution of a molecular cladogram is not good,
limited by the general extent of known paraphyly and extended paraphyly in
related well-sampled groups (if there are any). The many possible alternative
branching patterns supports many almost equally plausible hypotheses of
relationship, and thus the abduction of hypotheses is less efficient than
that of alpha taxonomy. The comparatively large sampling involved in alpha taxonomy allows a
focus on one best-by-far hypothesis for testing, in which case classification
may be changed based on abduction. But the restriction of sampling
distributions in molecular studies to one or very few specimens for species
or genera makes changing classifications to reflect molecular cladograms a
dubious practice. References Parker, B. 1988. Creation: The Story of the Origin and Evolution of
the Universe. Basic Books, Cambridge, Massachusetts. Springer, S. P. & G. Deutsch. 1993. Left Brain, Right Brain.
Fourth Edition. W. H. Freeman and Company, New York. |
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