You misunderstand sxb. What I suggested was that haplogroup T, alongside E1b1b-V32, was already present among Somalis prior to the medieval Futuh. I was just hypothesizing that the Futuh may have somehow skewed those original T frequencies; possibly through a population bottleneck. I based this mainly on the fact that haplogroup T appears to reach a frequency peak today in the former Adal Sultanate area.Jabuutawi wrote:Not quite. Wars with Abyssinia were comparatively recent events and had nothing to do with change in genetic composition of the populations. You are insinuating that the V-32 clade was predominant in the region, but that is not true. The population then, as now, were predominantly the same clans, hence same genetic markers, Hap T. It had less to do with bottleneck, and more to do (perhaps) with founder effect. I would believe your hypothesis if Futuh al-Habash occurred 5,000 years ago, not 500 years ago. In molecular evolution that is how long it takes for mutation to happen.
Timeline:
Haplgroup T is a rare and fairly young haplogroup, about 16K to 20K years old. Its origins were in the Levant. Back migrated to Africa and settled with E1b1b1 in southern Egypt/northern Sudan. Both drifted downward and finally settled in the Horn region, with Hap T getting to the Somali peninsula first about 2K years ago.
However, given the significant presence of both haplogroups E1b1b-V32 and T in the southern Egypt/northern Sudan area today, I agree that a founder effect from an ancestral migration from that area is more likely.

True walaal, haplogroup T is found at significant frequencies in the Northeast Africa corridor. A founder effect indeed makes sense since the autosomal ancestry of T-carrying Somalis is essentially the same as that of E1b1b-carrying Somalis.zumaale wrote:Why do you think that haplogroup T is not found between Southern Egypt and Northern Somalia in any significant numbers?
I ask this question because I am puzzled by how Somali T haplogroup carriers have a recent common ancestor going back 2000 or so years. This point towards a relatively recent founder effect among T Somalis. I am aware that with new technological advents in genetics, the TMCRA could be subject to change. However, it cannot be ruled out that the concentration of haplogroup T among certain Somalis could also be the result of overseas migration as it is a very young lineage in contrast to the surrounding cushitic E1b1b markers.
I guess a better picture will be obtained once a comparison has been made with the Egyptian T carriers.
Do you know what are the specific T haplotypes in the Somali territories? Are they closer to the Egyptian haplotypes or to the ones in Southern Arabia?