2018/02/11

January 2018: More Real World Evidence of Genetic Degeneration

January 2018: More Real World Evidence of Genetic Degeneration

http://www.geneticentropy.org/latest-development

Excerpt: "The newest edition of Genetic Entropy (2014), has shown that genetic degeneration is not just a theoretical concern, but is observed in numerous real-life situations. Genetic Entropy has reviewed research that shows: a) the ubiquitous genetic degeneration of the somatic cells of all human beings; and b) the genetic germline degeneration of the whole human population. Likewise Genetic Entropy has reviewed research that shows rapid genetic degeneration in the H1N1 influenza virus. Genetic Entropy also documents “evolution in reverse” in the famous LLEE bacterial experiment (article available here).
  • A new paper (Lynch, 2016) written by a leading population geneticist, shows that human genetic degeneration is a very serious problem. He affirms that the human germline mutation rate is roughly 100 new mutations per person per generation, while the somatic mutation rate is roughly 3 new mutations per cell division. Lynch estimates human fitness is declining 1-5% per generation, and he adds; “most mutations have minor effects, very few have lethal consequences, and even fewer are beneficial.”
  • Our new book “Contested Bones” (available at ContestedBones.org) cites evidence showing that the early human population referred to as Neanderthal (Homo neanderthalensis) was highly inbred, and had a very high genetic load (40% less fit than modern humans) (Harris and Nielsen, 2016; Roebroeks and Soressi, 2016). See pages pages 315-316. This severe genetic degeneration probably contributed to the disappearance of that population (PrÜfer et al., 2014; Sankararaman et al., 2014).
  • Similarly, the new book Contested Bones (pages 86-89), cites evidence that the early human population referred to as “Hobbit” (Homo floresiensis), was also inbred and apparently suffered from a special type of genetic degeneration called “reductive evolution” (insular dwarfing) (Berger et al., 2008; Morwood et al., 2004). This results in reduced body size, reduced brain volume, and various pathologies (Henneberg et al., 2014).
  • Contested Bones (pages 179-210) also cites evidence that the early human population referred to as Naledi (Homo naledi), was likewise inbred and suffered from “reductive evolution”, again resulting in reduced body size, reduced brain volume, and various pathologies.
  • Contested Bones (pages 53-75) also cites evidence that many other early human populations, broadly referred to as Erectus (Homo erectus), were inbred and suffered from “reductive evolution” (Anton, 2003). However, it seems the genetic degeneration of Erectus was less advanced—generally resulting in more moderate reductions in body size, brain size, and pathologies. Indeed, many paleoanthropologists would fold both Hobbit and Naledi into the more diverse Erectus category. 
  • An important but overlooked paper, written by leading population geneticists (Keightley et al., 2005), reported that the two hypothetical populations that gave rise to modern man and modern chimpanzee both must have experienced continuous genetic degeneration during the last 6 million years. The problems associated with this claim should be obvious. Their title is: Evidence for Widespread Degradation of Gene Control Regions in Hominid Genomes, and they state that there has been the“accumulation of a large number of deleterious mutations in sequences containing gene control elements and hence awidespread degradation of the genome during the evolution of humans and chimpanzees.” (emphasis added).
  • A new paper (Gaur, 2017), shows that if a substantial fraction of the human genome is functional (is not junk DNA), then the evolution of man would not be possible (due to genetic degeneration). Gaur states that human evolution would be very problematic even if the genome was 10% functional, but would be completely impossible if 25% or more was functional. Yet the ENCODE project shows that at least 60% of the genome is functional.
  • A new paper (Rogers and Slatkin, 2017), shows that mammoth populations were highly inbred and carried an elevated genetic load (likely contributing to their extinction due to “mutational meltdown”).
  • A paper (Kumar and Subramanian, 2002) shows that mutation rates are similar for all mammals, when based on mutation rate per year (not per generation). This means that mammals (both mice and men) should degenerate similarly in the same amount of time. This suggests that the major mutation mechanisms are not tightly correlated to cell divisions.
  • A new paper (Ramu et al., 2017), shows that the tropical crop, cassava, has been accumulating many deleterious mutations, resulting a seriously increasing genetic load, and a distinct decline in fitness.
  • Another paper (Mattila et al. 2012), shows high genetic load in an old isolated butterfly population. “This population exemplifies the increasingly common situation in fragmented landscapes, in which small and completely isolated populations are vulnerable to extinction due to high genetic load.”
  • Another paper (Holmes, E. C. 2003), shows that all RNA viruses must be young—less than 50,000 years. This is consistent with our H1N1 influenza study that show that RNA virus strains degenerate very rapidly."
My comment: Time will not rescue the theory of evolution. Time means degeneration. We can only observe rapid change in nature caused by epigenetic regulation of existing biological information OR gradual but inevitable disppearance of information.