Regular Member
Join Date: Jul 2003
Location: California
Posts: 454
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Quote:
Originally posted by Soralis
Let's take a look at some of those questions:
That would basically be the total number of organisms that lived, that were basically within the same species as those organisms that were among those directly along the fish-giraffe line. In one generation, this would be simply all the members of that species. Over a time span such as is involved here, it would be the sum of all the organisms of the species from which giraffes are direct descendants of.
That could be somewhat determined by looking at the genomes of the giraffe and fish, and noting the number of differences between the two. Of course, it's a bit more complicated then that.
First of all, there's the problem of for this to be straightforward, you'd need a 500 million year old fish (if you're going from the first fish to currently living giraffes, rather then from last common ancestor to those that fit into the species giraffe or family giraffidae or such), that would be an ancestor of current giraffes. If you took a currently living fish, it could have a common ancestor with a giraffe, but it also would have changed during all of that time period as well. You can still tell something from the difference there, since if the mutation rate is fairly close, or is known fairly well, then this can still be found out, since they would only start having a difference in mutations from the point of their most recent common ancestors.
There's also the other factor that not all mutations are of the same type, a duplication or inversion could produce a different sequence in far less mutations then point mutations could. Assuming you could recognize duplicated/inverted sequences that had some differences in them from other changes, you could recognize a number of those.
Now that would be much more difficult to account for, since that involves selection, and the environment of the organism. The actual changes wouldn't be made by selection, but if the changes are neutral, negative or positive would be. For example, in a lab situation, if I took a population of bacteria, and at every generation, I sequenced all of the bacteria, and killed any organism with a change, 100% of all changes would be negative. In the same situation, if I instead killed all organisms that were the same as their immediate ancestor, nearly all changes would be positive (the only ones that wouldn't be would basically be those that killed the organism or made it sterile).
To determine the rate of negative/neutral/positive changes would require the knowledge of the environment and situation of every generation, since that ratio would be different depending on the situation. And if you wanted to determine which mutations between fish and giraffe were -/0/+, would not only determine a knowledge of the environment and situation of each generation, but what specific changes were made when, and what changes and effects they had, given that environment, and given the rest of the genetic sequence that currently existed. There would be a greater proportion of them that would be positive, since it would be a descendant that would still be alive.
Hmm.. what do you mean by "fixed" in this context? From what you've previously said, it seems to mean that a specific allele has become very widespread within a population. (perhaps you mean to the exclusion of all other alleles, although that would probably be fairly rare in realistic situations.) Also, as the organisms involved are capable of sexual reproduction, the mutations would not have to happen in sequence from ancestor to descendant. In other words, you wouldn't have to have first one mutation in one generation, and then a second mutation with an organism that already had the first mutation. You could have both mutations arise separately in different organisms, that don't have the other mutation. Then, when those changes spread enough to the point where organisms with one mutation reproduce with organisms that have the other mutation, you can end up having an offspring that has both mutations. This means that the time for a mutation to become more common or fixed within a population isn't an issue for changes made affecting different areas. Different mutations can all happen separately from each other, and then come together in descendant populations. At least for those changes that might not work well without some other change in place. Those that would work better or need a certain other change to work well could still work in this fashion, as long as they could survive long enough on their own, although it's less likely, because of that reason. Which is why sideways transfer (in things such as sexual reproduction, plasmids, etc.) of genetic material is so useful. Since in organisms that reproduce asexually, and don't have such sideways transfer, one mutation would have to happen first, and then the other would have to happen in an organism that has the first, in order for a descendant to have both of them.
How fast a mutation spreads through a population, is dependent on how beneficial that mutation is. There are some equations for this that you can search for, on how fast a specific change will spread through a population, based on how likely an organism is to reproduce with that mutation over not having it, and give an estimate at how long it will take for it to be in a certain % of the population.
Well that depends what question you're asking, if you're asking what's the probability that the evidence that has been collected leads to the conclusion that this processes happened, I'd say so, that's basically been the whole point of this thread, except for a more general case. 
If on the other hand, you're asking that if you had a 500 million year old fish, what the probability of a giraffe being it's great^(200 million) grandchild or so, the probability would be extremely small, since it would rely on a large number of chance events and mutations that you couldn't predict in advance. Of course, there's no reason that a giraffe had to exist in the first place, so couldn't be used as an argument against it. It's like flipping a coin 100 times or so, before you flip the coin, the result of getting any particular sequence is the improbable 1/(2^100). However, that can't be used as an argument in reverse, about how that sequence couldn't happen after the fact, since that could be said about any sequence.
If you're asking more along the lines of if the rates of mutation and number of generations and organisms involved would produce the necessary variation in order for such a change to happen, that would be a bit more complex. As well as requiring some estimates of population size within generations and some other factors. You could get some estimates, based on the genetic difference between then two organisms, and how many changes would be necessary for that to happen, and to make it possible for those specific changes to happen.
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Excellent thoughts. And no, my point is not in the same category of your coin flipping analogy. Your final paragraph summarizes it better, though we'd need to add questions such as how many mutations are ever going to be helpful in getting to the giraffe; so that mutation rate alone is not sufficient. We'd need to consider how many mutations are harmful, or otherwise will never help get to the giraffe.
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