Curt Doolittle shared a link.
Source date (UTC): 2018-07-22 18:55:19 UTC
Curt Doolittle shared a link.
Source date (UTC): 2018-07-22 18:55:19 UTC
Curt Doolittle shared a post.
Source date (UTC): 2018-07-22 14:55:00 UTC
https://www.thecascadelegion.com/single-post/2018/07/22/Is-Leftism-a-Diseasehttps://www.thecascadelegion.com/single-post/2018/07/22/Is-Leftism-a-Disease
Source date (UTC): 2018-07-22 14:55:00 UTC
Source date (UTC): 2018-07-22 14:55:00 UTC
—“Lewontin and Gould were Marxist biologists who were so shameless about their ideology shaping their research that even left-leaning colleagues like Dawkins called them out.”— Matthew GenackLewontin: ‘greater variation within than across groups’ Gould: ‘mismeasure of man – cranium size is irrelevant’ What is “Lewontin’s Fallacy”? By Justin Smith, PhD Genetics and Heredity, Stanford University (2016) This is copied directly from Wikipedia but I think explains it well. Basically Lewontin’s argument was that because common genetic variation varies more between individuals than between races, race/ethnicitiy doesn’t really mean anything biologically, and that races/ethnicities aren’t real genetic categories. Human Genetic Diversity: Lewontin’s Fallacy “Lewontin’s argument In the 1972 study “The Apportionment of Human Diversity”, Richard Lewontin performed a fixation index (FST) statistical analysis using 17 markers, including blood group proteins, from individuals across classically defined “races” (Caucasian, African, Mongoloid, South Asian Aborigines, Amerinds, Oceanians, and, Australian Aborigines). He found that the majority of the total genetic variation between humans (i.e., of the 0.1% of DNA that varies between individuals), 85.4%, is found within populations, 8.3% of the variation is found between populations within a “race”, and only 6.3% was found to account for the racial classification. Numerous later studies have confirmed his findings.[5] Based on this analysis, Lewontin concluded, “Since such racial classification is now seen to be of virtually no genetic or taxonomic significance either, no justification can be offered for its continuance.” This argument has been cited as evidence that racial categories are biologically meaningless, and that behavioral differences between groups cannot have any genetic underpinnings.[6] One example is the “Statement on ‘Race’” published by the American Anthropological Association in 1998, which rejected the existence of races as unambiguous, clearly demarcated, biologically distinct groups.[7] Edwards’ critique: Edwards argued that while Lewontin’s statements on variability are correct when examining the frequency of different alleles (variants of a particular gene) at an individual locus (the location of a particular gene) between individuals, it is nonetheless possible to classify individuals into different racial groups with an accuracy that approaches 100 percent when one takes into account the frequency of the alleles at several loci at the same time. This happens because differences in the frequency of alleles at different loci are correlated across populations — the alleles that are more frequent in a population at two or more loci are correlated when we consider the two populations simultaneously. Or in other words, the frequency of the alleles tends to cluster differently for different populations.[8] In Edwards’s words, “most of the information that distinguishes populations is hidden in the correlation structure of the data.” These relationships can be extracted using commonly used ordination and cluster analysis techniques. Edwards argued that, even if the probability of misclassifying an individual based on the frequency of alleles at a single locus is as high as 30 percent (as Lewontin reported in 1972), the misclassification probability becomes close to zero if enough loci are studied.[9] Edwards’s paper stated that the underlying logic was discussed in the early years of the 20th century. Edwards wrote that he and Luigi Luca Cavalli-Sforza had presented a contrasting analysis to Lewontin’s, using very similar data, already at the 1963 International Congress of Genetics. Lewontin participated in the conference but did not refer to this in his later paper. Edwards argued that Lewontin used his analysis to attack human classification in science for social reasons.[9]” There are also real traits that vary a lot my ethnicity. Another argument against the Lewontin’s argument has to with rare or functional variation. For example sickle cell anemia is much more prevalent in subsaharan african populations than in the rest of the human population, and cystic fibrosis is much more prevalent in european populations than in the rest of the world.
—“Lewontin and Gould were Marxist biologists who were so shameless about their ideology shaping their research that even left-leaning colleagues like Dawkins called them out.”— Matthew GenackLewontin: ‘greater variation within than across groups’ Gould: ‘mismeasure of man – cranium size is irrelevant’ What is “Lewontin’s Fallacy”? By Justin Smith, PhD Genetics and Heredity, Stanford University (2016) This is copied directly from Wikipedia but I think explains it well. Basically Lewontin’s argument was that because common genetic variation varies more between individuals than between races, race/ethnicitiy doesn’t really mean anything biologically, and that races/ethnicities aren’t real genetic categories. Human Genetic Diversity: Lewontin’s Fallacy “Lewontin’s argument In the 1972 study “The Apportionment of Human Diversity”, Richard Lewontin performed a fixation index (FST) statistical analysis using 17 markers, including blood group proteins, from individuals across classically defined “races” (Caucasian, African, Mongoloid, South Asian Aborigines, Amerinds, Oceanians, and, Australian Aborigines). He found that the majority of the total genetic variation between humans (i.e., of the 0.1% of DNA that varies between individuals), 85.4%, is found within populations, 8.3% of the variation is found between populations within a “race”, and only 6.3% was found to account for the racial classification. Numerous later studies have confirmed his findings.[5] Based on this analysis, Lewontin concluded, “Since such racial classification is now seen to be of virtually no genetic or taxonomic significance either, no justification can be offered for its continuance.” This argument has been cited as evidence that racial categories are biologically meaningless, and that behavioral differences between groups cannot have any genetic underpinnings.[6] One example is the “Statement on ‘Race’” published by the American Anthropological Association in 1998, which rejected the existence of races as unambiguous, clearly demarcated, biologically distinct groups.[7] Edwards’ critique: Edwards argued that while Lewontin’s statements on variability are correct when examining the frequency of different alleles (variants of a particular gene) at an individual locus (the location of a particular gene) between individuals, it is nonetheless possible to classify individuals into different racial groups with an accuracy that approaches 100 percent when one takes into account the frequency of the alleles at several loci at the same time. This happens because differences in the frequency of alleles at different loci are correlated across populations — the alleles that are more frequent in a population at two or more loci are correlated when we consider the two populations simultaneously. Or in other words, the frequency of the alleles tends to cluster differently for different populations.[8] In Edwards’s words, “most of the information that distinguishes populations is hidden in the correlation structure of the data.” These relationships can be extracted using commonly used ordination and cluster analysis techniques. Edwards argued that, even if the probability of misclassifying an individual based on the frequency of alleles at a single locus is as high as 30 percent (as Lewontin reported in 1972), the misclassification probability becomes close to zero if enough loci are studied.[9] Edwards’s paper stated that the underlying logic was discussed in the early years of the 20th century. Edwards wrote that he and Luigi Luca Cavalli-Sforza had presented a contrasting analysis to Lewontin’s, using very similar data, already at the 1963 International Congress of Genetics. Lewontin participated in the conference but did not refer to this in his later paper. Edwards argued that Lewontin used his analysis to attack human classification in science for social reasons.[9]” There are also real traits that vary a lot my ethnicity. Another argument against the Lewontin’s argument has to with rare or functional variation. For example sickle cell anemia is much more prevalent in subsaharan african populations than in the rest of the human population, and cystic fibrosis is much more prevalent in european populations than in the rest of the world.
https://www.jihadwatch.org/2018/07/turkish-government-using-us-mosques-to-spread-islamist-nationalistic-fervorhttps://www.jihadwatch.org/2018/07/turkish-government-using-us-mosques-to-spread-islamist-nationalistic-fervor
Source date (UTC): 2018-07-21 16:30:00 UTC
Source date (UTC): 2018-07-21 16:30:00 UTC
they still do.
Source date (UTC): 2018-07-21 15:40:43 UTC
Original post: https://twitter.com/i/web/status/1020695072646541312
Reply addressees: @danqueseq
Replying to: https://twitter.com/i/web/status/1020683863549456385
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Original post: https://twitter.com/i/web/status/1020683863549456385
Curt Doolittle shared a post.
EUGENICS VS. DYSGENICS
by Ely Harman
Eugenics is the tendency of genes to get “better.” It relates to politics because all policies are either Eugenic, they tend to make genes better, or they are “dysgenic,” they tend to make genes “worse.”
I understand the definitions of “better” or “worse” are going to be a stumbling block for most people, since they seem kind of subjective. But I believe they have more or less objective definitions, at least as related to policy. A policy is eugenic if it selects for the genes that enable the policy to be carried into effect. And it is dysgenic if it selects for genes that disrupt, retard or arrest the policy itself or against genes that the policy relies upon.
E.g. Insisting people feed themselves is a eugenic policy because it selects for people who can feed themselves, and against people who can’t. There is no systemic failure mode. Things only get better over time as individuals who fail to feed themselves remove their failure genes from the gene pool. But feeding people is a dysgenic policy because it selects for people who can’t feed themselves and against people who can feed them (the ability to feed people who can’t feed themselves becomes a burden, risk, and cost, because it carries the obligation to do so.) Thus, the latter policy will tend to break down over time as people who can’t feed themselves proliferate and the people who can feed them are consumed. But a eugenic policy can be maintained indefinitely and be built upon continuously.
Put another way, Eugenia is the gradual, sustainable, accumulation and inprovement of genetic capital, that can be built upon with further improvements, while dysgenia is its consumption for the short term propagation of defective garbage.
Accumulation vs. consumption. Production vs. parasitism. Eugenia vs. dysgenia.
Source date (UTC): 2018-07-21 12:35:03 UTC