In your posts 260, 261, 265 and 266 you set out your arguments in support of your position that belief in a literal Adam and Eve is warranted. In this, and subsequent posts, I intend to show why such a belief is unwarranted if one applies the standards of a well and broadly educated reasonable person. In your posts you make much of the claim that belief in a literal Adam and Eve is warranted in the context of Christian philosophy. This is not a valid argument on its own for assenting to a proposition about human origins that is amenable to investigation using the methods of natural science. Where there is a conflict between evidence available from the natural world and arguments based on philosophical reflection or pure reason, one needs to make a judgment about the relative strength of the evidence from the natural world and the philosophical reasoning. In this case, the natural science arguments against the existence of a literal Adam and Eve are compelling and the philosophical arguments you put forward in support of the idea are flawed.
**The natural science arguments are compelling. **
The existence of a literal Adam and Eve implies that all humans alive today descend from a single pair of parents who are the first representatives of a new species and who represent a sharp demarcation between humanity and other animals. The molecular and palaeontological evidence indicates otherwise. First, the number of ancient lineages at highly polymorphic loci arithmetically exceeds that which can pass through a bottleneck of two individuals; second, considerations from population genetics based on multiple studies using a range of methods on many different loci concur that the effective human population through Palaeolithic times is about 10,000 which is inconsistent with a bottleneck of two; third, the existence of a number of ancient haplotypes in nuclear genes is inconsistent with a simple single origin for modern humans and an extreme population bottleneck; fourth, the palaeontological evidence is that human powers of technology, language, symbolism, abstract thought and so on evolved gradually over more than a million years. Let’s look at each of these.
Various investigations of highly polymorphic loci in the primate genome, such as the Class II MHC genes, DRB1, DQB1 and DPB1 conclude that many more than four allelic lineages predate the divergence of humans and chimpanzees. Although recent work by Bergstrom et al have shown that amongst the 618 (!) known human alleles at DRB1 (Holdsworth et al, The HLA Dictionary 2008,
Tissue Antigens 73, 95 – 170 (2009)) many rare alleles are of recent (ie in the last 500,000 years) origin, all studies have concluded that a substantial number of allelic lineages predate the divergence of humans and chimpanzees:
Ayala, The myth of Eve, Molecular biology and human origins,
Science 270, 1930 – 1936
Ayala and Escalate, The evolution of human populations: a molecular perspective. Mol Phylogenet Evol 5,188–201.
Ayala et al, Molecular genetics of speciation and human origins, PNAS 91, 6787 – 6794 (1994)
Bergstrom et al, Recent Origin of DRB1 alleles and implications for human evolution, Nature Genetics 18, 237 (1998)
Bergstrom et al, Phylogenetic history of hominoid DRB1 loci and alleles inferred from intron sequences, Immunological reviews 167:351-365 (1999)
Klein J. & C. O’hUigin: Class II B Mhc motifs in an evolutionary perspective.
Immunol Rev 143, 89-112 (1995)
Code:
In addition, other work shows that DR haplotypes (DR1 to DR16 of DRB1, and DR51 to DR53 of DRB3, DRB4 and DRB5) predate the divergence of human and chimp; for example:
Gongora et al, The HLA-DRB9 gene and the origin of HLA-DR haplotypes, *Human Immunology *51, 23 –31.
Svensson et al, Evolutionary relationship between human major histocompatibility complex
HLA-DR haplotypes,
Immunogenetics 43, 304 - 314
Since two individuals can carry, at most four different alleles at any given locus (and four different haplotypes of the class II region of the MHC), it is arithmetically impossible for the human lineage to have passed through a bottleneck of two (even if we ignore the fact that in a tiny population, one or more of those alleles might well drift to extinction). The Shiina paper that you cited against this is irrelevant to this conclusion (in fact it is irrelevant to the questions of human demography and phylogeny altogether) for reasons that I have already pointed out (primarily because the study is methodologically incapable of revealing any information about the phylogeny of the human DRB1 locus – I assume that you will read and absorb my more detailed explanation in my earlier post for why that is so and refrain from repeating the irrelevant quotation from the paper).
to be continued