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Member (Idle past 4979 days) Posts: 228 From: jo'burg, RSA Joined: |
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Author | Topic: Can Domestic Selection cause Macroevolution? | |||||||||||||||||||||||||||
Wepwawet Member (Idle past 6134 days) Posts: 85 From: Texas Joined: |
Hi folks, new poster here although I've been lurking for a while.
If we limit this topic to animals I don't think we can reasonably expect to see speciation within the 15,000 or so years which have passed since we started domesticating animals. The art and eventual science of animal husbandry which allows us to breed for or against specific traits has been around for considerably less time. Most domestic animals have a life expectancy of from 10-20 years (considerably less for animals bred specifically for meat which is a much more recent practice than other uses). And we have long recognized the advantages of bringing in new blood to strengthen stock lines(including the addition of wild members of the species). Both factors which should reduce expectations of seeing speciation within domestic animals. I believe the case has been made that we have seen speciation within domesticated plants. I just wonder if that's sufficient for the critics. On a side note to Faith who thinks meanings change too fast, I'd like to remind you that we're communicating in a living language that grows and changes as we do. We can't expect words to hold the same meaning forever unless we want to invent words as fast as we change. How much good would it do me to tell you that while macroevolution has never been observed, grizification has? As a party to this conversation you are just as responsible as the writer for understanding the meaning and context of the writer. Since this is a science forum you should also realize that the scientific definition for any particular word is usually more appropriate than the common definition. If I look up the word in a dictionary I can immediately see that the word can be used in many ways:
quote: If I look a little harder (okay it's really on the same page) I can find medical dictionaries to help me understand how a scientist might use the word:
quote:Source: Species Definition & Meaning | Dictionary.com Just as long as the writer used the word with a meaning similar to one of the above definitions (and not a definition from say the 1930 edition), a reasonable reader can be expected to understand exactly what the writer means. Playing word games looks like an attempt to dodge the underlying issue. When science and the Bible differ, science has obviously misinterpreted its data. - Henry Morris, Head of Institute for Creation Research |
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kuresu Member (Idle past 2539 days) Posts: 2544 From: boulder, colorado Joined: |
i would reply that they did not pick this path, and without our intervention the version of corn we eat would have died (never mind never having been created). There's nothing symbiotic about this relationship. Unless you want to call mankind a bunch of parasites.
when did I assume that we would suddenly disappear? What if we were to just stop eating corn?
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Belfry Member (Idle past 5111 days) Posts: 177 From: Ocala, FL Joined: |
kuresu writes:
This is nonsensical. What does "picking a path" have to do with the discussion?
i would reply that they did not pick this path... kuresu writes:
Everything dies, the issue in this case is reproduction. Domesticated maize now requires us for part of its life cycle, just like in any other obligate symbiosis (from mutualism to parasitism). One way of looking at it is that domesticated maize is well-adapted to exploit humans as a highly efficient dispersal agent. As I have pointed out, it has proven to be a very effective strategy for this lineage. ...and without our intervention the version of corn we eat would have died (never mind never having been created) This is not at all unusual. Flowering plants have developed structures allowing them to exploit insects and other animals for pollination, and specialized fruit to employ animal seed dispersers. Their animal counterparts have also adapted to better benefit from the relationship. This is coevolution in a nutshell.
kuresu writes:
I have demonstrated that both humans and maize, as species, benefit from their interaction in the same way that other well-documented symbiotic organisms do in nature (such as ambrosia beetles and their fungi). If you think you can refute this, please do so. Your comment about parasitism is a non sequitur, as far as I can tell.
There's nothing symbiotic about this relationship. Unless you want to call mankind a bunch of parasites. kuresu writes:
Well, disappear from the interaction, anyway - same issue and same problems with your statement. when did I assume that we would suddenly disappear? What if we were to just stop eating corn? This message has been edited by Belfry, 04-05-2006 08:41 PM
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crashfrog Member (Idle past 1492 days) Posts: 19762 From: Silver Spring, MD Joined: |
There's nothing symbiotic about this relationship. Unless you want to call mankind a bunch of parasites. Symbiosis is not the same as parasitism. Symbiosis is defined as a relationship between two dissimilar species that is both intimate and potentially obligatory. Largely, the contiuum of symbiotic relationships can be described as: 1) Mutualism, where the two organisms each benefit from the relationship;2) Commensuralism, where one organism benefits and another is not affected; 3) Parasitism, where one organism benefits to the detriment of another. The relationship between humans and our crops could certainly be described as mutualism, and therefore does qualify as a symbiotic relationship. Humans benefit from the food source provided by corn; Zea mays mays certainly benefits from human husbandry to the extent that it has become the world's most popular and profitable cereal crop. This message has been edited by crashfrog, 04-05-2006 09:09 PM
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kuresu Member (Idle past 2539 days) Posts: 2544 From: boulder, colorado Joined: |
when I said died, I should have said become extinct. As far as I know, in no symbiotic relationship (in which there are those three types: commensualism, parasitism, and mutualism) does one alter the other for its own purpose.
and if you remember, in first post on this topic I said I may have been shooting myself in the foot. evolution, as I understand it, has no pre-picked paths. It is not goal-oriented. Birds did not develop wings in order to fly, but fly becasue they have wings. We did not develop a brain in order to think, but rather think becasue we have a brain. I might need to clarify this at a later point. The corn, as for that matter all domesticated crops and animals, have been selected for with specific goals in mind. With corn, it was to produce a plant that would provide us with a better food source. Why do you think we introduced Russian wheat to the US? Russian wheat is better at surviving winters, and it would not surprise me that we have been hybridizing for that trait with our own wheat.
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kuresu Member (Idle past 2539 days) Posts: 2544 From: boulder, colorado Joined: |
Symbiosis is not the same as parasitism. really? you contradict yourself later on
the contiuum of symbiotic relationships can be described as: 1) Mutualism, where the two organisms each benefit from the relationship;2) Commensuralism, where one organism benefits and another is not affected; 3) Parasitism, where one organism benefits to the detriment of another. another contradiction
relationship between humans and our crops could certainly be described as mutualism, and therefore does qualify as a symbiotic relationship if mutualism is one type of symbiotic relationship, which the defintion you provide earlier does say, then how can you claim that mutualism is not symbiotic, or parasitism for that matter?
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kuresu Member (Idle past 2539 days) Posts: 2544 From: boulder, colorado Joined: |
hey, this is this dudes brother. while i can see where you're coming from i think, which is that they are three completly different definitions but the only problem there is if you take two of the three that fall under symbitotic relationship there is only one left and though the english language is messed up why would they make two completly different words for the same thing and the other two you discluded fall under symbiotic relationship due to both of these definitions which makes your argument completly pointless along with the fact that you cannot even argue a simple arguement even a little bit on the good side. and although these is one extremly one long run on sentence it still makes more sense then your pitifull excuse for an argument.
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Quetzal Member (Idle past 5898 days) Posts: 3228 Joined: |
As far as I know, in no symbiotic relationship (in which there are those three types: commensualism, parasitism, and mutualism) does one alter the other for its own purpose. Just a point of correction: a number of parasites induce behavioral or other changes in their hosts - especially intermediate hosts. One example: Robb T, Reid ML, 1996 “Parasite-induced changes in the behaviour of cestode-infected beetles: Adaptation or simple pathology?”, Canadian Journal of Zoology/Revue Canadien de Zoologie. Vol. 74, no. 7, pp. 1268-1274.quote: I think this is a pretty clear indicator that at least sometimes parasites DO alter their hosts for their own benefit.
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Belfry Member (Idle past 5111 days) Posts: 177 From: Ocala, FL Joined: |
kuresu writes:
Conscious intent is immaterial, though it may make the process more efficient. The process in non-human examples is much the same as in human agriculture; crops which are more beneficial to the cultivator (be it human or insect) are selected for, deleterious phenotypes are selected against. Not until we developed more direct genetic manipulation techniques (gene insertion and such) did human methods fundamentally differ from this process.
when I said died, I should have said become extinct. As far as I know, in no symbiotic relationship (in which there are those three types: commensualism, parasitism, and mutualism) does one alter the other for its own purpose. kuresu writes:
This is essentially correct... it's not necessarily goal-oriented, but even if evolution is guided by humans, with humans as the primary NS agent and with a human goal in mind, it's still evolution.
evolution, as I understand it, has no pre-picked paths. It is not goal-oriented. Birds did not develop wings in order to fly, but fly becasue they have wings. We did not develop a brain in order to think, but rather think becasue we have a brain. I might need to clarify this at a later point. kuresu writes:
Well, I think it is arguable whether the Native Americans foresaw what would result when they started to cultivate that native annual grass, or whether they just preferentially cultivated varieties that arose on their own. The corn, as for that matter all domesticated crops and animals, have been selected for with specific goals in mind. With corn, it was to produce a plant that would provide us with a better food source. Why do you think we introduced Russian wheat to the US? Russian wheat is better at surviving winters, and it would not surprise me that we have been hybridizing for that trait with our own wheat. In any case, I agree that human consciousness and forethought are unique in contributing to these interactions. However, "domestic selection" still isn't a fundamentally a different process from natural selection. The more beneficial plants are still selected as more "fit," it's just that human perception is the primary determinant of fitness in that case.
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kuresu Member (Idle past 2539 days) Posts: 2544 From: boulder, colorado Joined: |
Everyone, please ignore the post my brother made. He's a bit rude, if you couldn't tell, and while he can think, its a touch difficult to understand him a times. And I need to remember to log off when I'm finished.
As far as I can tell, I'm defending the OP, in that NS and DS are two different processes. I wasn't aware of the parasites changing the behavior of the hosts, but does this have an affect on that host's evolution? The answer is most likely yes, but I should probably read that paper in full before I open my mouth. I'm not sure how one can equate a human as being the agent of NS in the domestication of animals and plants. In ToE, fitness is measured by the number of offspring one has and some other factors dealing with those offspring (if I'm not mistaken). If one has more offspring, the more your genes are present, and if they are beneficial, they will eventually become the dominant phenotype. That is the fitness of NS. The fitness we look for in crops and animals is not their ability to produce successful offspring, but their ability to provide us with a better yield. This fitness is not the same as that in NS, and therefore DS becomes a corrupted version.
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AdminJar Inactive Member |
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kuresu Member (Idle past 2539 days) Posts: 2544 From: boulder, colorado Joined: |
agreed.
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U can call me Cookie Member (Idle past 4979 days) Posts: 228 From: jo'burg, RSA Joined: |
Whoa! Didn't expect this topic to blow up overnight.
Welcome Faith Glad you could join us. Nothing like a bit of YEC interjection to get the pulses racing on this forum...
All I had in mind was that domestic selection is more intense and focused than natural selection, so that the level of genetic changes you'd expect to see if macroevolution is true would be seen there first. It was a way of saying that while natural selection provided Darwin with the needed explanation for how macroevolution MIGHT occur, it didn't do anything to show that it HAS occurred, which could be demonstrated just as well by artificial selection if there's anything to the idea. That's just it tho, Faith. DS is a lot more intense than NS. It is this increase in intensity that would possibly limit its macroevolutionary potential. For macroevolution to occur (and i am using a speciational definition*, will get to this just now), variation (old and new) is required. DS often results in a much faster decrease in variation than NS; so much so that it could restrict the function of variation in speciation. Apart from the above, DS is strongly directed. Humans breed for the characteristics they want. This, added to the weakened effect of variation and drift, could also, intuitively, restrict macroevolution; since humans aren't breeding FOR macroevolution. Then,to bring in a point that Ned raised, macroevolution is not only about Selection. There are other factors involved. Some that, maybe, would lend to DS causing speciation, and some that would take away from this possibility. it should be noted, I'm not saying that speciation is impossible under DS; just that it is, intuitively, less likely. *Speciation in the sense that two different species are genetically incompatible. I do this since there is no reason to set macroevolution at a higher taxonomic level, which are usually just arbitrary anyway.Fact is, i've noticed that it is often the case that anti-evolutionists get to "set the limits", and evolutionists usually just accomodate them. I don't see why this should be the case, and i tire of it. (Any reply to this particular statement should be taken to the Microevolution vs Macroevolution thread. "The good Christian should beware the mathematician and all those who make empty prophecies. The danger already exists that the mathematicians have made a covenant with the devil to darken the spirit and to confine man in the bonds of hell." - St. Augustine
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Mammuthus Member (Idle past 6501 days) Posts: 3085 From: Munich, Germany Joined: |
I found a few studies in plants addressing some of the issues brought up here. For example
Genetics. 2006 Jan;172(1):457-65. Epub 2005 Sep 12. Related Articles, Links Genetic variation and selection response in model breeding populations of Brassica rapa following a diversity bottleneck. Briggs WH, Goldman IL. Department of Horticulture, University of Wisconsin, Madison, Wisconsin 53706, USA. whbriggs@wisc.edu Domestication and breeding share a common feature of population bottlenecks followed by significant genetic gain. To date, no crop models for investigating the evolution of genetic variance, selection response, and population diversity following bottlenecks have been developed. We developed a model artificial selection system in the laboratory using rapid-cycling Brassica rapa. Responses to 10 cycles of recurrent selection for cotyledon size were compared across a broad population founded with 200 individuals, three bottleneck populations initiated with two individuals each, and unselected controls. Additive genetic variance and heritability were significantly larger in the bottleneck populations prior to selection and this corresponded to a heightened response of bottleneck populations during the first three cycles. However, the overall response was ultimately greater and more sustained in the broad population. AFLP marker analyses revealed the pattern and extent of population subdivision were unaffected by a bottleneck even though the diversity retained in a selection population was significantly limited. Rapid gain in genetically more uniform bottlenecked populations, particularly in the short term, may offer an explanation for why domesticators and breeders have realized significant selection progress over relatively short time periods. So genetic gain in the selected (bottleneck populations) can lead to rapid diversification i.e. potential macroevolution...but the trait being selected is fairly broad as opposed to most DS scenarios..this makes this study a bit more realistic in terms of NS. A similar study in butterflies
Genet Res. 2001 Apr;77(2):167-81. Related Articles, Links Effects of bottlenecks on quantitative genetic variation in the butterfly Bicyclus anynana. Saccheri IJ, Nichols RA, Brakefield PM. Research Group in Evolutionary Biology, Institute of Evolutionary and Ecological Sciences, University of Leiden, Kaiserstraat 63, PO Box 9516, 2300 RA Leiden, The Netherlands. saccheri@liverpool.ac.uk The effects of a single population bottleneck of differing severity on heritability and additive genetic variance was investigated experimentally using a butterfly. An outbred laboratory stock was used to found replicate lines with one pair, three pairs and 10 pairs of adults, as well as control lines with approximately 75 effective pairs. Heritability and additive genetic variance of eight wing pattern characters and wing size were estimated using parent-offspring covariances in the base population and in all daughter lines. Individual morphological characters and principal components of the nine characters showed a consistent pattern of treatment effects in which average heritability and additive genetic variance was lower in one pair and three pair lines than in 10 pair and control lines. Observed losses in heritability and additive genetic variance were significantly greater than predicted by the neutral additive model when calculated with coefficients of inbreeding estimated from demographic parameters alone. However, use of molecular markers revealed substantially more inbreeding, generated by increased variance in family size and background selection. Conservative interpretation of a statistical analysis incorporating this previously undetected inbreeding led to the conclusion that the response to inbreeding of the morphological traits studied showed no significant departure from the neutral additive model. This result is consistent with the evidence for minimal directional dominance for these traits. In contrast, egg hatching rate in the same experimental lines showed strong inbreeding depression, increased phenotypic variance and rapid response to selection, highly indicative of an increase in additive genetic variance due to dominance variance conversion. Also, corn after domestication changed in macroevolutionary terms but also regained genetic diversity quickly even though coalescence suggests a founder population of only 20 individuals
Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4441-6. Related Articles, Links Investigation of the bottleneck leading to the domestication of maize. Eyre-Walker A, Gaut RL, Hilton H, Feldman DL, Gaut BS. Department of Plant Sciences and Center for Theoretical and Applied Genetics, Rutgers University, New Brunswick, NJ 08902, USA. Maize (Zea mays ssp. mays) is genetically diverse, yet it is also morphologically distinct from its wild relatives. These two observations are somewhat contradictory: the first observation is consistent with a large historical population size for maize, but the latter observation is consistent with strong, diversity-limiting selection during maize domestication. In this study, we sampled sequence diversity, coupled with simulations of the coalescent process, to study the dynamics of a population bottleneck during the domestication of maize. To do this, we determined the DNA sequence of a 1,400-bp region of the Adh1 locus from 19 individuals representing maize, its presumed progenitor (Z. mays ssp. parviglumis), and a more distant relative (Zea luxurians). The sequence data were used to guide coalescent simulations of population bottlenecks associated with domestication. Our study confirms high genetic diversity in maize-maize contains 75% of the variation found in its progenitor and is more diverse than its wild relative, Z. luxurians-but it also suggests that sequence diversity in maize can be explained by a bottleneck of short duration and very small size. For example, the breadth of genetic diversity in maize is consistent with a founding population of only 20 individuals when the domestication event is 10 generations in length. And from mammals, it shows depending on how one selects, the populations can separate (macroevolution) or merge
J Anim Sci. 1991 Jun;69(6):2387-94. Related Articles, Links
Selection within and across populations in livestock improvement. Smith C, Banos G. University of Guelph, Ontario, Canada. Genetic evaluations within and across populations (countries, breeds, herds) allow ranking on estimated genetic merit and selecting breeding individuals across populations. Selection within and across populations (combined selection) should by definition always be as good as, or better than, within-population selection, the limiting case. The advantage depends on the sizes of the populations, the number of populations, the initial genetic means, and the correspondence of the breeding objectives in the different populations, as measured by the genetic correlation for economic merit. The advantages of combined selection are evaluated deterministically for a simple case of selecting the best males for use across populations by using a common truncation line over the distributions of EBV for the different populations. Combined selection increases overall response rates in the cooperating populations. Where the initial genetic means are the same, small populations (100 males tested) benefit greatly from combined selection. Large populations (500 to 1,000 males tested) also benefit, but less. The results depend on the increased selection response to scale, response being approximately linear with the logarithm of the number tested. When the initial means differ, the genetically poorer population can catch up in three to five generations and then contribute to the increased responses with combined selection. When breeding objectives differ, selection usually gradually pulls the populations apart and they make less and less contribution to each other and finally become separate. These results have implications for breeding strategies. Their application would affect structures of populations and rates of genetic change possible by selection.
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Mammuthus Member (Idle past 6501 days) Posts: 3085 From: Munich, Germany Joined: |
Always great to have you around with references! Makes the rest of us have to scramble to get them and catch up
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