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12-23-2002, 04:59 PM | #31 | |
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Try harder next time. |
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12-23-2002, 05:04 PM | #32 | ||||||||||||||
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Do you have any knowledge of population genetics at all? Quote:
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"Just so stories" are plausible explanations invented in the complete absence of supporting evidence. We do have evidence of long term change in the history of life on this planet -- but if it is brought up, I'm sure you'll start chanting the usual silly creationist litany of "were you there?" Quote:
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And again, what do you know of population genetics? Your claim that drift only happens in "tiny, isolated populations" again suggests that you don't know anything about it -- that is a false statement. Quote:
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Again, you seem to be completely oblivious to what the theory of evolution actually says. Natural selection is not considered a major factor in speciation. Quote:
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12-23-2002, 05:37 PM | #33 | |
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Can you please explain why it is not or provide a link that does? Thanks, Rick |
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12-23-2002, 05:58 PM | #34 | |
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Disruptive selection would be an exception, but even there a process that does not involve selection had to be present to generate the range of heritable variation that is subsequently selected for the extremes. |
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12-23-2002, 06:21 PM | #35 |
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That makes sense; thanks
Rick |
12-23-2002, 06:27 PM | #36 |
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Hey, pz...once again THANKS! I learned something new about evolution today. I guess that's roughly what I was thinking when I was thinking "dieback" in my other thread. Let me see then if I've got this strait-speciation seems to always involve some kind of isolation of a population, be it Darwin's finches on islands or Neanderthal man in Europe. So in nature, then the reason that we have so many species of say, beetles in Hawaii is that there are many small ecological niches that these animals can fill. Also, beetles don't travel especially well, so it would make sense in a pre-human populated Hawaii for beetles to perhaps occupy one small area and become isolated by drift and isolation. Do I understand this correctly or am I still off in my thinking somewhere? Bubba |
12-23-2002, 06:29 PM | #37 | |
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12-23-2002, 06:30 PM | #38 |
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Oh, and by the way on behalf of thiests everywhere I apologize for Evolskeptics actions.
We now return you to your regularly scheduled debate. Bubba |
12-23-2002, 08:39 PM | #39 |
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Hello again, Evolskeptic.
Tip number 1 of web etiquette, if you don't want to be flamed, don't light the first match. Our rules do still apply to you, so I request that you cut out the imflamatory posts and stick to the topic at hand. Now, if you'd rather deal with just one poster at a time, I'd be happy to engauge you in a debate in our structured debate forum. I have been waiting for almost a year for a creationist to take me up on my challenge to debate the existance/inexistance of multiple immutable kinds. Are you willing to spar with me? If not, is there a topic that you would be willing to debate me in? However, before you accept, let me intorduce myself. I am a second-year graduate student in the Department of Genetics at the University of Georgia. I study evolutionary theory with respect to population genetics. Most of my work involves mathematical and computational modeling of flucuating gene pools. I currently have three projects: a frequency-dependent selection model for the evolution of language ability, an evolutionary algorithm for data mining of cyto-nuclear data, and a stocastic density dependent model for density-vagueness. PZ already covered most of my points but I have one thing to add. Earlier you said you couldn't be bothered with studying evolutionary theory, specifically the constant viability selection model. However, I happen to have already exposed the board to it in <a href="http://iidb.org/cgi-bin/ultimatebb.cgi?ubb=get_topic&f=58&t=000207&p=" target="_blank">this thread</a>. I will assume that you have read it when I make the following statements. A result of the model is that the change in allele frequency of a trait between generations is d=p*(1-p)*(w1-w2)/wbar. Thus it is clear from (w1-w2) that the change in the frequency an allele is proportional to the advantage that it has over the other allele. Directional selection (w11 >= w12 >= w22, one or no inequalities strict) is all that is required to drive an allele to fixation. It doesn't matter how strong the selection is, thus your "secret" doesn't exist. ~~RvFvS~~ |
12-23-2002, 08:40 PM | #40 | |
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I can't wait. |
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