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Guide to Patagonia's Monsters & Mysterious beings

I have written a book on this intriguing subject which has just been published.
In this blog I will post excerpts and other interesting texts on this fascinating subject.

Austin Whittall


Showing posts with label Bottleneck. Show all posts
Showing posts with label Bottleneck. Show all posts

Friday, April 24, 2026

Higher mutation accumulation in Europeans vs. Africans


Another paper mentioning different mutation rates in Africans and non-Africans!


The paper by Mallick, S., Li, H., Lipson, M. et al. The Simons Genome Diversity Project: 300 genomes from 142 diverse populations. Nature 538, 201–206 (2016). https://doi.org/10.1038/nature18964, reported that "Our analysis reveals key features of the landscape of human genome variation, including that the rate of accumulation of mutations has accelerated by about 5% in non-Africans compared to Africans since divergence."


The branch-length issue


This reminded me of a recent post I wrote about Short branch lengths in Africans for Y-chromosomes. Branch lengths are linked to accumulated mutations (the lenght of a branch is the number of mutations in it) so if we start from the fork where Africans and non-Africans split, the branch of Africans is shoreter because it has accumulated fewer mutations, while the non-African one is longer, as it has more accumulated mutations. In that post I asked "...but we are all the same age and equally distant from our common ancestor. So why do the Africans have fewer mutations? Do Eurasians accumulate more mutations?"


I also went back to reread a recent post Mutation rate is faster in Africa where I mentioned different studies suggesting that a higher diversity in Africans (measured by their heterozygosity) promoted a higher mutation rate or μ. But Mallick, Li and Lipson et al. in their 2016 paper suggest otherwise. I quote them below and highlight their findings, which seem to baffle them:


"More mutation accumulation in non-Africans than in Africans
The SGDP data provide an opportunity to compare the rates at which mutations have accumulated across populations. We restricted our analyses to samples for which our genotypes are likely to be most reliable ... We pooled samples by region to increase power, and for all pairs of regions, computed the expected number of positions where, if we picked a random chromosome from both, region A would mismatch chimpanzee and region B would be identical to chimpanzee (or vice versa). If the rate of accumulation of mutation has been the same since the two populations diverged, these numbers are expected to be equal. However, when we compute the ratio of mutations on one lineage or the other since separation, we find a subtle (average of 0.5%) but significant excess of mutations in nonAfricans relative to sub-Saharan Africans. Because any difference must reflect events since non-African / African population divergence which is a less than a tenth of average genetic divergence, this implies a greater difference in mutation accumulation rates since population divergence (~5%). We were concerned that these results might be biased by the fact that the human genome reference sequence is more closely related to non-Africans than to Africans, or by higher levels of heterozygosity in Africans, as both these issues could make detection of divergent sites in Africans more difficult. However, we replicated the findings after remapping to chimpanzee, which is equally distant to all present populations, and after restricting analyses to the X chromosome in males (males only have a single X chromosome, and so this procedure avoids bias due to different error rates in detecting heterozygous genotypes in populations with different rates of heterozygosity). These observations are most likely to be explained by acceleration in the rate of mutation accumulation in non-Africans, since the same signal appears in comparisons to sub-Saharan Africans related in different ways to non-Africans. It is known that the rate of CCT>CTT mutations differs across human populations. However, this particular mutation class was found to be enriched relative to Africans in Europeans but not in East Asians, and thus cannot explain our signal. One of several possible explanations for these findings is a decrease in the generation interval in non-Africans compared to Africans since separation...
"


What is going on?


Mallick, S., Li, H., Lipson, M. et al. affirm that mutations accumulate at a higher rate in non-Africans than within Africa, this does not mean that mutation rates (μ) are different, it means that the mutations are fixed differently. It is also higher among Europeans than East Asians. To explain it they propse that non-Africans have a shorter "generation time": they are mating at a younger age than Africans so they accumulate more generations in a given span of time, and therefore more mutations than Africans in the same period.

Generation Time

I am surprised because other research has shown that longer generation times lead to more mutations because "each additional year of paternal age results in an average of 3.9 × 10−10 more mutations per base per generation (Source) and hunter-gatherer people nowadays have longer generation ages (32.3 years for fathers) than sedentary groups and because older fathers accumulate more mutations, if Africans are mating at an older age, there will be more mutations. There is something that isn't adding up here!


A similar viewpoint was reported by Wang and Obbard, 2023: "Our analysis also shows that mutation rates increase significantly with increasing generation time... The relationship we observe between generation time and per-generation mutation rate could therefore be a consequence of either a greater number of cell divisions or of accumulating damage over time." Which makes sense.


However, not all agree, research conducted by Lewin and Eyre-Walker, 2025 confirms that mutation rate (μ) and generation time are inversely correlated (longer generation time = lower mutation rate; and shorter generation time = higher mutation rate).


Due to these conflicting findings, until consensus is reached, for the time being I will leave generation times out of the matter and look for other plausible causes for the higher number of mutations in non-Africans vs. Africans.


Other causes explaining higher accumulation of mutations


Effective population size or Ne. Wang and Obbard, 2023, also notice that "populations with larger Ne tend to have a lower mutation rate even after accounting for their shorter generation times." Africans are said to have a larger initial Ne due to the bottleneck effect that affected those leaving Africa, a small subset of the large original population. The authors suggest that if "... species with small Ne tend to have a longer generation time, and a longer generation time causes higher mutation rates then a higher μ in species with low Ne could be driven by a mechanistic generation-time effect." Since Eurasians seem to have both factors (small Ne and low generation times) is seems logical that their mutation rate is higher.


Besides the effective population size and generation time, there are more possible explanations for the shorter branch in Africans and the longer one in Eurasians are: natural selection, that removes noxious mutations, so looking back from the present, the mutations never seem to have taked place because they were not fixed. Reduced DNA repair mechanisms, one group has a less efficient repair mechanism for mutations and these tend to accumulate in comparison to another group with a more efficient repair system.


The increased TCC→TTC mutation rate in Europeans


This factor is mentioned in Mallick, S., Li, H., Lipson, M. et al. as a possible explanation. But, what does it really mean? I will quote from Harris and Pritchard, 2017, who studied the matter.


Our DNA is made up of two backbones, the intertwined helixes linked by "steps" like a ladder, made from bases called Guanine (G), Cytosine (C), Thymine (T) and Adenine (A). Guanine always links to Adenine G—A, and Thymine with Cytosine (C—T) bonds. Looking at the steps of one side of the helix you will see a sequence like "ATCGATTGAGCTCTAG", and opposing it, on the other strand the complementary bases: "GCTAGCCAGATCTCGA".


Research has shown that "European people experience more mutations within certain DNA motifs (specifically, the DNA sequences ‘TCC’, ‘TCT’, ‘CCC’ and ‘ACC’) than Africans or East Asians do." Why?


Harris and Pritchard propose that "the rate of TCC→TTC mutations increased dramatically ∼15,000 years ago and decreased again ∼2000 years ago... [and] hypothesize that this mutation pulse may have been caused by a mutator allele that drifted up in frequency starting 15,000 years ago, but that is now rare or absent from present day populations." They go on to explain the cause: " At this time, we cannot exclude a role for nongenetic factors such as changes in life history or mutagen exposure in driving these signals. However, given the sheer diversity of the effects reported here, it seems parsimonious to us to propose that most of this variation is driven by the appearance and drift of genetic modifiers of mutation rate."

So it seems that it is due to a chance appearance of genes that regulate mutation rates.


A curious yet interesting fact is that the same effect of TCC→TTC mutation increase is observed in East Asian cattle! It appeared in two separate mammal groups, indicine cattle, derived from the Bos taurus indicus and humans but outside of Africa (Talenti, et al., 20216)


A challenge to the "stable" molecular clock


Harris, 2015 also looks into the TCC→TTC subject and says that explaining the cause is beyond the scope of the paper. However, Harris concludes that "Even if the overall European mutation rate increase was small, it adds to a growing body of evidence that molecular clock assumptions break down on a faster timescale than generally assumed during population genetic analysis. It was once assumed that the human lineage’s mutation rate had changed little since we shared a common ancestor with chimpanzees, but this assumption is losing credibility due to the conflict between direct mutation rate estimates and molecular-clock-based estimates. Although this conflict might have arisen from a gradual decrease in the rate of germline mitoses per year as our ancestors evolved longer generation times, the results of this paper indicate that another force may have come into play: change in the mutation rate per mitosis. If the mutagenic spectrum was able to change during the last 60,000 years of human history, it might have changed numerous times during great ape evolution and beforehand."


I agree, mutation rates are variable, and conclusions based on a constant rate will be wrong.


Notice how different papers find opposite effects (faster mutation rates in Africans, or in Europeans), and don't quite understand the reason!



Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2026 by Austin Whittall © 

Sunday, February 15, 2026

Neutral Theory of Genetic Evolution and Out Of Africa


The main backing for the Out of Africa theory is the Genetic Neutrality Theory.


The arguments of an African origin of modern humans and our dispersal across the globe is supported by the high genetic diversity found in modern African populations, with lower diversity elsewhere, and a gradient or cline in diversity that reflects less diversity as distance to the African homeland increases. Both of these factors are expected according to the Neutrality Theory.


Starting with a highly diverse population, if a small group from that population migrates (into Eurasia), it can only feasibly carry with it a sub-sample of the original diversity. This is known as a Founder Effect, the founders of a new population carry fewer genes than the population from which they split from.


This happened time and time again, as sub-sub-groups split from the main population and moved into Europe, Eastern, Northern, and Southern Asia, Melanesia, Australia, Polynesia, and across North America, and then, into South America.


The Neutral Theory states that each split reduces genetic diversity.


Genetic Heterozygosity


Heterozygosity is a measure of diversity. Each person receives genes from their parents, that code for different proteins and produce traits. Those who have two different varriants (alleles) of a specific gene, one inherited from each parent are heterozygous. If the alleles are identical, they are homozygous.


The image below shows two parents (both are heterozygous) each carrying two different variants A and a. The probability for passing them on to the next generation is simple there are four possible combinations, each has a 25% probability of occurring:


heterozygosity and homozygosity
Hetero and Homozygosity. Copyright © 2026 by Austin Whittall

The chances are that two of the offspring will carry Aa alleles, and will therefore be heterozygous, while the other two will receive the same allele from each parent and be either AA or aa, carrying two identical copies. This makes them homozygous.


As we can see, a population that is 100% heterozygous as become 50% homozygous and 50% heterozygous. All the possible combinations of those homozygous and heterozygous genes are shown below:

allele combinations
Combinations of alleles. Copyright © 2026 by Austin Whittall

As you can see 25% of each variant (AA, aa, Aa, and aA). So why would heterozygosity decrease? Suppose only aa homozygous couples mate, the chance of this happening is 1 in 16, or AA mate, again, 1 in 16. So 2:16 or, 1:8 chance of only homozygous mating and offspring. But... if these offspring meet and mate aa with AA, they would have a 100% heterozygous descent. This is true for large populations, but for smaller groups the founder effects and bottlenecks can reduce the allele diversity.


Genetic Bottlenecks


The argument of loss of heterozygosity, or its equivalent, increase in homozygosity is based on genetic bottlenecks, where a small sub-population splits and carries with it the homozygous variant, say only aa or only AA. Losing the possibility of reintroducing the lost allelle. This is a 1 in 16 chance.


Other causes of heterozygosity loss are natural catastrophes, war, and disease. But, why would such events affect the heterozygous individuals more than the homozygous. Wouldn't they be random, and therefore have an equal chance of impacting on hetero- and homozygous individuals?


Regarding the root population. There is the chance that the root from which a population split off from suffered some event that eliminated a large swath of it, while the migrating sub-population in another geographic location was not affected by it. Wouldn't that lower the heterozygosity of the basal group and make the sub-population appear as "enriched"?


Genetic Drift


Both Founder effect and Bottlenecks are part of process called Genetic Drift. As we saw, genetic drift takes place when random events, by chance modify which alleles passed on by parents to their offspring. They also include not only non-reproduction of certain individuals due to war, disease, natural catastrophes, but also loss of genetic variation due to people who don't reproduce because they die before mating, choose not to do so, etc. Genetic Drift isn't driven by evolution. The random changes may or may nor provide adaptations to a changing environment, so they may or not be acted upon by the forces of natural selection.


A sub-population may lose certain alleles, or others may become Fixed reaching a 100% frequency in the population due to chance events.


Mutations and Natural Selection


Random mutations take place, and modify the alleles, natural selection may also work, favoring the survival of individuals with alleles that provide adaptative benefits.


But, what about mutations, that happen by chance, that have a deleterious effect? Some mutations may have harmful consequences. The Neutral theory says that some deleterious mutations may rise to high frequencies in small populations due to fixation promoted by genetic drift. But, why wouldn't people carrying unfavorable genes be affected by natural selection, causing them and their descent to die out?


The Neutral Theory of Molecular Evolution


It was the creation of Motoo Kimura, who in 1968 proposed that at a molecular level, mutations are caused by random genetic drift. These mutations are neutral from a selective point of view. They aren't affected by natural selection.


Kimura has been criticized, for instance Kern and Hahn (2018), argue that modern, genome-scale data demonstrates far more evidence of adaptive evolution than the neutral theory allows, suggesting that natural selection (both positive and negative) shapes much of the genome.


As mutations take place by chance, the probability of them being neutral, deleterious, or beneficial would seem equivalent. So, why assume they are neutral? A beneficial mutation even if it is rare would confer an evolutionary advantage for those carrying it, and modify the population beyond what neutral models suggest.


Linked Selection. The loci (or addresses) that mark the location (locus) of a gene in our DNA isn't independent and isolated. Some genes or DNA sequences located close together on the same chromosome are inherited together, as a unit, during meiosis (linked chromosomes).


Selective Sweep is when an allele that improves the fitness of its carrier increases in frequency due to natural selection, is accompanied (hitchhiking) by other genes linked to it by physical proximity on the DNA strand are also increased in frequency even though they may be neutral. Finally, Background Selection is similar and has the opposite effect: deleterious alleles are removed by natural selection and neighboring neutral alleles are lost too, due to physical proximity to the harmful variants.


These examples show that "neutrality" is not necessarily true.


Molecular Clock


Kimura's theory states that neutral mutations took place at a constant speed, accumulating over time at the same pace. However, this is not true.


However mutations don't appear in a uniform manner in all loci along the genome, they arise unequally, and the probability of fixation depends on where they arise in the genome. This modifies how the clock ticks (Source). Furthermore, substitutions depend on population size, and generation overlap (Source).


Generation time is also an important factor: is it 20 or 30 years? 25? or 18? Over 10,000 generations this means a time scale that can vary from 180,000 to 300,000 years!


Back-Mutations and Recurrence Not Allowed


Kimura's theory, at least when applied in practice, has three axioms that are not true:

  1. Infinite sites, it assumes that each mutation takes place at a site that has never mutated before.
  2. No back-mutations, changes happen in one direction A → G. Which will never again flip back G → A
  3. No Recurrence, in practice there are multiple mutations that take place at the same site. The neutral theory does not accept it, there can't be multiple mutations at identical loci in different lineages.

A paper gives a great example of why and how a back-mutation can have positive effects (here showing how a base C = Cytosine mutates to T = Thymine and back):


"...simple back-mutation is expected to generate slightly advantageous mutations. For example, let us imagine that a site is fixed for C, and that a new T mutation occurs that is slightly deleterious with a disadvantage of −s. Let us imagine that this T mutation spreads through the population and becomes fixed. If a new C mutation then occurs at this site, it will be slightly advantageous with an advantage of +s, unless the relative fitnesses of the C and T alleles have changed. Such a change in fitness could occur because of a change in the environment or the fixation of mutations at other sites which have epistatic interactions with the alleles at a site of interest."


Americas: Great Dying


Regarding Amerindian diversity, we know that up to 90%, or more, of the Native Americans died during the century that followed European "discovery". Disease, war, famine, social disruption, force labor, etc. killed tens of millions of Amerindians. Lineages died out, massively. This is the unique and most massive genocide (albeit unplanned) in the history of humanity. How can we know the number of unique, diverse, divergent alleles that were wiped out during this event? In 1491, America probably presented a far more diverse genetic structure than it does now.

And this brings us to the other point: African "diversity".


African Diversity... is it real?


Finally, and this will be the subject of a future post, do modern Africans reflect the genetic makeup of ancient Africa 100,000 or 75,000 years ago? Is a modern Nigerian, Gambian, Angolan African representative of the ancient population from which the Out of Africa migrants split? Have other events taken place within Africa, isolated from the sub-population that migrated into Eurasia? Admixture with archaic hominins after the OOA event, admixture between many separate and formerly isolated hunter gatherer sub-populations could have led to a modern highly diverse African population, while the original OOA root was far less diverse.



Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2026 by Austin Whittall © 
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