Please hold while I work out the "redundancy"
Without wedging in either the current ID or Darwinworship sense and more space for genetics, it might be possible to state more than metaphorically,
quote:
" the subset of genes in one species is greater than the set of all genes of all species,"
Where "of genes" refers to Johannsen but the set refers to parts of expressible genes susceptible to recombinant techniques only emphasis is on the subjective problem in the word "species" than the objective ostentation of "genes."
I know my work below is too confident and written only "for me" just now but I see no reason that if proved by actual statistical information that vitally it is not insignificant to what may prevent abduction to all macro-issues.
As for which is the larger number... well that depends through the ordertype whether the FIRST one was manifested in thought as a cardinal of ordinal before...etc.
Mendel’s “Developmental” Bionomial, Boole, and Relational Database Normal Forms - Using 1-D Frieze Patterns to take apart the the “+” in the symbolization of “A+2Aa+a”
ABSTRACT--During a period in the history of biology that SJ Gould feels can be phased, organismic biologists realized that they had not properly focused on their level of preference, the organism, as molecular biology advanced. This has resulted in various versions biophilosophy and the plausible relations of contingency to form-making and translation in space among creatures. The cause of this failure in inution of a phenotype is due to failure in the history of logic to extend its line of thought theoretically far enough to be incident with outlines of form-making that might be co-ordinated Cartesiastically. Advances in the molecular nature of inheritance provide a means to support Mendel’s original use of the form of maths’ bionomial through the use “ornaments.” The traditional/classic/standard explanation that a disagreement over adaptive vs non-adaptive traits was the “fall guy” is thus shown false and the actual reason becomes a failure to project theoretical structures into the area of visible comparative ability, subjectively held by biologists. Application is made to the biology of Lichens and a potential niche construction among Cicadas, CicadaKiller Parasitic Wasps and Fowler’s Toads.
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Olby wrote 93/4:” Added to this evidence is the well-known absence of double letters to represent the pure breeding offspring of hybrids in Mendel's scheme. Thus the three classes in this second hybrid generation (F2) are given the symbols: A + 2Aa + a rather than AA + 2Aa + aa. If these letters refer to the hereditary elements or factors to which Wilhelm Johannsen later gave the name 'gene', we would expect Mendel to have used double letters for each class. To defend Mendel's claim to the gene concept geneticists have indulged in special pleading thus: 'It is but an abridged way of expression. It was perfectly clear to Mendel that those elements occurred paired in homozygotes . . .' Or: 'throughout the papers (and even in his later correspondence with the botanist Ngeli) he has described the three classes of individuals in an F2 as A, Aa and a, evading the unproved doubleness of the "homozygote" AA class.' “
Olby's "Mendel, Mendelism, and Genetics," at MendelWeb
This is why I take apart the “+” rather than focus on sexual group selection issues over the sign”\” between pollen and seed etc generalized to any living thing.
The reason that the unknown or neutral phenotype arose by the early 70s was because the “doubleness” that differentiates the work of Fisher, Haldane or Wright , (Kimura etc) is false and due to a decomposable situation statistically where a ring field replaces a Cartesian space but because Russell ruled against a particular kind of mathematical proof about “ limits” the narrow focus of Boole’s x^2 only dominated the language of biology such that not even the restrictions of Woodger’s attempts (or others analytically) could be furthered within the organism and instead the plan was frustrated by criticism outside biology (creationism etc) This false double or false positive can be recomposed by splitting the “/” sign into group theory symbols of 1-D Freize patterns when ordinated to actual effective population numbers.
The lie is thus given to “overcrowding” as the first and foremost image of the surface of transformative biological potential and the notion(Gould SETH 473) of wedging(Darwin) is shown erroneous because the Mendelization of population genetics with Freize pattern decompositions has increased the place of genetic rotation and revolution (Gould on Goldschmidt and D’Arcy Thompson (Gould SETH 463”He then praises D’Arcy Thompson for locating the phyletic meaning of these ideas in small mutational changes in rates, operating early in development to yield saltational origin of a new adult phenotypes”’’ “)without altering the mathematics of analytic geometry. The prejudice of 2-D is revealed as “saltational origin” and first order logic only in relational databases constricted by the historical relay from Boole’s resticted rules to X^2 only, in “perception.”
In the mean-time I for one have to remain content with my own marginilzation here:
quote:
Edited by Brad McFall, : justification