dust1n
Zindīq
That organisms carry useless garbage around for 3000 generations, at which point it suddenly becomes useful, is not a working model. In the model that would mean the organisms become garbage, rather than that they carry garbage around.
Sigh... welcome back, Mohammad. I can see your fixation with refuse-based vocabulary hasn't left.
I'm aware you'd yet to have a luxury of taking a couple of evolutionary biology courses, so Ii'll drop this here:
"Genetic drift (or allelic drift) is the change in the frequency of a gene variant (allele) in a population due to random sampling of organisms.[1] The alleles in the offspring are a sample of those in the parents, and chance has a role in determining whether a given individual survives and reproduces. A population's allele frequency is the fraction of the copies of one gene that share a particular form.[2] Genetic drift may cause gene variants to disappear completely and thereby reduce genetic variation...
The law of large numbers predicts that when the population is large, the effect of genetic drift is much milder. When the reproductive population is small, however, the effects of sampling error can alter the allele frequencies significantly. Genetic drift is therefore considered to be a consequential mechanism of evolutionary change primarily within small, isolated populations.[25]
Although both processes affect evolution, genetic drift operates randomly while natural selection functions non-randomly. While natural selection has a direction, guiding evolution towards heritable adaptations to the current environment, genetic drift has no direction and is guided only by the mathematics of chance.[26] As a result, drift acts upon the genotypic frequencies within a population without regard to their phenotypic effects. In contrast, selection favors the spread of alleles whose phenotypic effects increase survival and/or reproduction of their carriers, lowers the frequencies of alleles that cause unfavorable traits, and ignores those that are neutral.[27]
In natural populations, genetic drift and natural selection do not act in isolation; both forces are always at play, together with mutation and migration. However, the magnitude of drift on allele frequencies per generation is larger when the absolute number of copies of the allele is small, e.g. in small populations. The magnitude of drift is large enough to overwhelm selection when the selection coefficient is less than 1 divided by the effective population size.
The mathematics of genetic drift depend on the effective population size, but it is not clear how this is related to the actual number of individuals in a population.[13] Genetic linkage to other genes that are under selection can reduce the effective population size experienced by a neutral allele. With a higher recombination rate, linkage decreases and with it this local effect on effective population size.[28][29] This effect is visible in molecular data as a correlation between local recombination rate and genetic diversity,[30] and negative correlation between gene density and diversity at noncoding sites.[31] Stochasticity associated with linkage to other genes that are under selection is not the same as sampling error, and is sometimes known as genetic draft in order to distinguish it from genetic drift.[13]
When the allele frequency is very small, drift can also overpower selection even in large populations. For example, while disadvantageous mutations are usually eliminated quickly in large populations, new advantageous mutations are almost as vulnerable to loss through genetic drift as are neutral mutations. Not until the allele frequency for the advantageous mutation reaches a certain threshold will genetic drift have no effect.[27]
In general, "global" solutions to many adaptive challenges at once can evolve at a smaller effective population size than "local" solutions that must evolve separately to each adaptive challenge.[32]""
https://en.wikipedia.org/wiki/Genetic_drift