I'm assuming you simply misspoke here, because all creationists deny speciation.
Not at all. The changes have to conform to the conditions that foster them.
Yes, and for some reason those limits prevent speciation.
What do you see as the relevant difference?
Really! Boy, I've been here on RF for quite some time now and I've seldom seen any confusion over either term. Almost without fail:
Evolution, as it stands in opposition to creationism, posits the evolution of species.
Creationism claims that god created all species as is.
And I assume you believe some of this testable and verifiable evidence proves YEC claims to be true and evolution to be wrong. If so, please share.
Sorry, but I'm a bit ignorant of why and how the mechanics of evolution are so limited as to prevent speciation. Any help will be appreciated.
Thanks.
But there is no such dilemma.
The Claim
J. B. S. Haldane calculated that new genes become fixed only after 300 generations due to the cost of natural selection (Haldane 1957). Since humans and apes differ in 4.8 × 107 genes, there has not been enough time for difference to accumulate. Only 1,667 nucleotide substitutions in genes could have occurred if their divergence was ten million years ago.
The Response
1. Haldane's "cost of natural selection" stemmed from an invalid simplifying assumption in his calculations. He divided by a fitness constant in a way that invalidated his assumption of constant population size, and his cost of selection is an artifact of the changed population size. He also assumed that two mutations would take twice as long to reach fixation as one, but because of sexual recombination, the two can be selected simultaneously and both reach fixation sooner. With corrected calculations, the cost disappears (Wallace 1991; Williams n.d.).
Haldane's paper was published in 1957, and Haldane himself said, "I am quite aware that my conclusions will probably need drastic revision" (Haldane 1957, 523). It is irresponsible not to consider the revision that has occurred in the forty years since his paper was published.
2. ReMine (1993), who promotes the claim, makes several invalid assumptions. His model is contradicted by the following:
The vast majority of differences would probably be due to genetic drift, not selection.
Many genes would have been linked with genes that are selected and thus would have hitchhiked with them to fixation.
Many mutations, such as those due to unequal crossing over, affect more than one codon.
Human and ape genes both would be diverging from the common ancestor, doubling the difference.
ReMine's computer simulation supposedly showing the negative influence of Haldane's dilemma assumed a population size of only six (Musgrave 1999).
source
For references see linked article.
The role of horizontal gene transfer needs to be explored as well as the evolutionary mechanisms of natural mutations, natural selection, gene flow, genetic drift, and genetic recombination for the emergence of genetic diversity generational changes of a population's gene pool.
Cosmic ancestry theory can often explain the transitional evolutionary changes between species that aren't well-explained by traditional Darwinian evolution.
Viruses can insert new genes, which have never before encountered by a species, to become part of the species' genome. These transferred genes are a vital part evolution. According to Cosmic Ancestry, the horizontal transfer of genes by viruses and other means is essential for evolutionary progress.
Three New Human Genes
and De Novo Genes in General |
What'sNEW
Entirely novel human-specific protein-coding genes originating from ancestrally noncoding sequences have been reported by two geneticists at the University of Dublin
Reference:
David G. Knowles and Aoife McLysaght, "Recent de novo origin of human protein-coding genes" [abstract], doi:10.1101/gr.095026.109,
Genome Research, online 2 Sep 2009.
Discovery of novel genes..., by EurekAlert!, 1 Sep 2009.
Genes That Make Us Human, by Elizabeth Pennisi, ScienceNOW, 1 Sep 2009.
Three human genes evolved from junk, by Michael Le Page, NewScientist, 3 Sep 2009.
Which Genes Make Us Human? by Alan Boyle, MSNBC, 3 Sep 2009.
."Analyzing available data, they identified genes that are expressed in the human species but not in chimps. They then looked for simiar sequences in other primates, finding three. The chimp and macaque (unexpressed) sequences are nearly identical to the human one, but are interrupted by frameshifting insertions and stop codons.
Although the three human genes are known to be expressed from several lines of evidence, their functions are not definitively characterized. However one, chronic lymphocytic leukemia upregulated gene 1 (
CLLU1), appears to have a role in that human disease. Its sequence among humans, compared to the matching one in chimps and macaques, is illustrated below.
"Multiple sequence alignment of the gene sequence of the human gene
CLLU1 and similar nucleotide sequences from the syntenic location in chimp and macaque. The start codon is located immediately following the first alignment gap, which was inserted for clarity. Stop codons are indicated by red boxes. The sequenced peptide identified from this locus is indicated in orange. The critical mutation that allows the production of a protein is the deletion of an A nucleotide, which is present in both chimp and macaque (indicated by an arrow). This causes a frameshift in human that results in a much longer ORF capable of producing a 121-amino acids-long protein. Both the chimp and macaque sequences have a stop codon after only 42 potential codons." © Genome Research 2009
CLLU1 is also disabled by a matching point insertion in the gorilla and gibbon, but not orangutan, genomes. The geneticists reason,
If the ancestral primate sequence was coding, then we would need to infer that an identical 1-bp insertion occurred in four lineages independently, whereas if we infer the presence of the disabler in the ancestral sequence, then we must infer two independent 1-bp deletions. The inference that the ancestral sequence was noncoding is a more parsimonious explanation of the data, even without considering that the parallel insertion of a specific base into an identical location is probably less likely than the parallel deletion of one base. ...We hypothesize that these genes have originated de novo in the human lineage, since the divergence with chimp from ancestrally noncoding sequence.
Consider the human nucleotide sequence designated
CLLU1, 121 codons in length. A codon, three nucleotides, may encode any of 20 amino acids, or a stop. (But this sequence is a gene, an open reading frame with no stops.)
Assume that the protein encoded by this nucleotide sequence needs ~25%, or 30, of its codons exactly right. In other words, only 1 out of 21 codons can occupy each of those 30 positions. The chance that 30 random codons will match this sequence in one trial can be estimated as
(1/21)^30 = ~10^-40
Assume that the remaining 91 codons in this sequence may vary widely, encoding any of 10 of life's 20 amino acids, but no stops. In other words, 10 out of 21 codons can occupy each of those 91 codon positions. The chance that 91 random codons will satisfy these criteria in one trial is approximately
(10/21)^91 = ~10^-30
Combining these assumptions, the chance that a given sequence of 121 random codons will constitute a working version of this gene is on the order of
10^(-40-30) = 10^-70 ..."
(This method copies Chandra Wickramasinghe's in
The Legacy of Fred Hoyle, reviewed
2005.)
Reference:
Metazoan Genes Older Than Metazoa?, 25 Oct 1996.
"If a new genetic program arrives by the strong panspermia process, intervening (ancestral) species should possess either nearly identical versions of it ...or nothing similar.."
Reference:
New genetic programs in Darwinism and strong panspermia, 7 Apr 2002.
.At least some of the silent DNA is for future use ."]Reference:
Why Sexual Reproduction?, first posted May 1996.
"Point mutations and other simple mechanisms can switch existing programs off and on."
Reference:
Testing Darwinism versus Cosmic Ancestry, 24 Nov 2002
"This process would ...depend on sophisticated software management that can recognize an installed program."
Reference:
Duplication Makes A New Primate Gene, 21 Feb 2005.
"New genetic programs will be continually offered for testing."
Reference:
How is it Possible?, first posted May 1996.
The human genome has 145 "alien" genes that can't be linked to any of our distant past ancestors; these genes are in our genome from the process of horizontal gene transfer. These 145 human genes, which nobody inherited from any distant past ancestor, might have been the result of genetic engineering by advanced extraterrestrial intelligence.
Reference:
Expression of multiple horizontally acquired genes is a hallmark of both vertebrate and invertebrate genomes
Genome Biology201516:50
Expression of multiple horizontally acquired genes is a hallmark of both vertebrate and invertebrate genomes
- Received: 25 September 2014
- Accepted: 4 February 2015
- Published: 13 March 2015
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