Huh?
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THWOTH wrote:The mode of the creationist shows scant regard for things like facts, evidence or an honestly representing information. One of their main argumentative tactics involves promoting the idea that "science invalidates science" in some way.
With that in mind, one can imagine any number of creationist arguments around Mendel, such as:
a) scientists and biology teachers have always told us that evolution operates according to Mendel's strict model of generic inheritance.
b) since the 1970s scientists have understood that the deterministic Mendelian model of inheritance is not how DNA, genes, chromosome, and therefore evolution, actually works.
c) therefore everything you have heard or been taught about Mendel, and how his ideas are supposed to sit at the very foundation of evolution, is not just wrong, but an out-and-out lie.
d) therefore the only possible alternative explanation for life on Earth is 'god did it'.
Just guessing here though.
collecemall wrote:THWOTH wrote:The mode of the creationist shows scant regard for things like facts, evidence or an honestly representing information. One of their main argumentative tactics involves promoting the idea that "science invalidates science" in some way.
With that in mind, one can imagine any number of creationist arguments around Mendel, such as:
a) scientists and biology teachers have always told us that evolution operates according to Mendel's strict model of generic inheritance.
b) since the 1970s scientists have understood that the deterministic Mendelian model of inheritance is not how DNA, genes, chromosome, and therefore evolution, actually works.
c) therefore everything you have heard or been taught about Mendel, and how his ideas are supposed to sit at the very foundation of evolution, is not just wrong, but an out-and-out lie.
d) therefore the only possible alternative explanation for life on Earth is 'god did it'.
Just guessing here though.
Given my mental abilities right now I'm doing good to remember to come back and check the follow up messages here yet alone the genetics courses I took 10 or so years ago or high school biology some 25+ years ago. I know this would be a very simplified explanation but are b) and c) the case because the mendelian model doesn't account for the random nature of mutations and how they would impact DNA/genes/etc. and how they are selected? Don't feel obligated to spend an inordinate amount of time trying to explain if it's significantly more complex and you don't know of an easy resource to point me at for an explanation.
To be honest I don't really expect most of the creationists I run into to be able to articulate what it is they are arguing when more often than not they don't even really have a rudimentary understanding of what evolution includes/precludes. Typically I've found the folks here (and other similar forums) know the arguments the creationists are trying to make even if the creationist does not. So I thought it worth a shot asking here. I just had not seen this particular beast out in the wild before and encountered it 4-5 times across two threads in a short span of time. If I get a better grasp of what it is they seem to be getting at or a miracle occurs and they'll actually cite the argument for me I'll come back and possibly try again. I'm hopeful some of this cognitive fog I'm dealing with will eventually lift and maybe I can answer it for myself.
Thanks to both of you for your response.
collecemall wrote:Long term lurker, rare poster, middling mental abilities. So please be gentle and if needed move this to a more appropriate subforum etc.
collecemall wrote:Anyway, I keep encountering commenters making claims that mendelian genetics are a barrier to evolution. I vaguely remember doing the squares in general biology in high school and can't remember anything from the two college level genetics courses I took online that would create issues for evolution. I'm really not even sure what it is they seem to be arguing other than because there are dominant and recessive genes that this somehow precludes evolution? I realize this is not a fantastic way of explaining an argument I'm running into and an even worse way to then ask "what the hell are they on about?" but I thought if anyone has seen this argument these forums would be the place to find out A) what is it they are trying to argue? and B) If there isn't an obvious counter can you give me a short explanation of why it is/isn't an issue. A couple of the comments seemed to focus on the inability of hybrids to reproduce as well. Which again I'm not sure how that precludes evolution in some way. I've asked a couple of them how this is a barrier and so far have not gotten coherent responses when I've gotten them at all. I should probably just forget about it but I'm seeing this way too frequently for them to not be getting this from somewhere. One of the typical offenders (DI/AIG/etc) has to have put this out at some point which I guess is what I'm counting on for you guys to have seen.
collecemall wrote:
... are b) and c) the case because the mendelian model doesn't account for the random nature of mutations and how they would impact DNA/genes/etc. and how they are selected?
Andersson, 1982 wrote:
Darwin's1 bypothesis that male secondary sexual ornaments evolve through female preferences is theoretically plausible2-7, but there is little field experimental evidence that such preferences exist8-10. I have studied female mate choice in relation to male tail length in the Long-Tailed Widowbird, Euplectes progne, and report here that males in which the tail was experimentally elongated showed higher mating success than males having normal or reduced tail. The possibility that intrasexual competition among males maintains the long tail was not supported; males with shortened tails held their territories as long as did other males. These results suggest that the extreme tail length in Long-Tailed Widowbirds is maintained by female mating preferences.
Calilasseia wrote:I'll elaborate a little on what Spearthrower has presented above in his usual succinct manner.
Back in the 1970s, tropical fishkeepers specialising in the breeding of domesticated Betta splendens (Siamese Fighting Fish) found an unusual mutation appearing in their stocks - the Double Tail mutation.
Fish inheriting this mutation have two tails. Interestingly, the two tails in question are not arranged side by side, as is the case with domesticated Fantail or Veiltail Goldfish, but stacked vertically - what I refer to as an "over-under shotgun" arrangement). Each tail has its own caudal plate, and associated musculature.
Now it transpires that a single gene is implicated in this mutation, and that gene exhibits single-factor Mendelian recessive inheritance. But wait, it's also selectable, at least in the aquarium environment. Females are more powerfully attracted to Double Tail males than their single tail relations, and this can be demonstrated experimentally in the requisite setup. You'll find I've been fairly prolific with respect to discussing Double Tail Betta splendens here.
Note my caveat above, about this being selectable in the aquarium environment. I'll explain now in more detail.
In the wild, females of the species have relatively short fins, while males have somewhat longer fins (though nowhere near as long as in in aquarium bred specimens). There's a tradeoff - longer male finnage makes the males more attractive to females for mating purposes, but fins that are too long impede escape from predators to a potentially lethal extent. The wild environment therefore exhbiits two selection pressures - one arising from sexual selection, driving the emergence of longer male finnage, and the other from natural selection, curbing the extent of that male finnage extension.
In the aquarium, of course, threats from predators are removed. Consequently, mutants that would not survive in the wild, with the sort of enormously extended finnage seen in many aquarium specimens, can survive happily under human care, and breed. If you perform the requisite experiments, a female of the species, given a choice between several wild type males and aquarium bred males with much enhanced finnage, choose the aquarium males for mating. The more luxuriant the finnage, the greater the effect, and since Double Tail males have some of the most luxuriant finnage of all, they are powerfully sexually selectable in the aquarium.
Indeed, if those fish could survive in the wild, humans would not have needed to wait for mutants to appear in aquarium stocks, as natural forces would already have driven the appearance and preservation of those mutants in the wild. They would be the norm, not an exception restricted to the aquarium environment.
If you need another example to see this in action, look at Mexican Resplendent Quetzals (Pharomacrus mocinno). Males of this bird species have outlandish tail feathers, the appearance of which was driven by sexual selection on the part of the females. Females lack such ornamentation, and have tail feathers of more conventional length. Quite simply, any phenotype (and its underling genotype) will establish itself in a population if sufficient selection pressure exists to do so.
Possibly even more outrageous looking is the Long-Tailed Widowbird, Euplectes progne, which again exhibits tail feather elongation in males, and a fair amount of research has been published into the operation of sexual selection in this species. Perhaps the classic paper on this is the one documenting an experimental test of sexual selection in this species, viz:
Female Choice Selects For Extreme Tail Length In A Widowbird by Malte Andersson, Nature, 299: 818-820 (28th October 1982) [Paper can be found here, though sadly behind a paywall].
From that paper:Andersson, 1982 wrote:
Darwin's1 bypothesis that male secondary sexual ornaments evolve through female preferences is theoretically plausible2-7, but there is little field experimental evidence that such preferences exist8-10. I have studied female mate choice in relation to male tail length in the Long-Tailed Widowbird, Euplectes progne, and report here that males in which the tail was experimentally elongated showed higher mating success than males having normal or reduced tail. The possibility that intrasexual competition among males maintains the long tail was not supported; males with shortened tails held their territories as long as did other males. These results suggest that the extreme tail length in Long-Tailed Widowbirds is maintained by female mating preferences.
Quite simply, the first port of call when dealing with creationist assertions, is the primary peer reviewed scientific literature, which invariably informs the honest reader that creationists are lying.
Oh, by the way, if you want an example of a test of sexual selection that you yourself can perform in your own home, try this from Ole Seehausen:
The Effect Of Male Colouration On Female Mate Choice In Closely Related Lake Victoria Cichlids (Haplochromis nyererei Complex) by Ole Seehausen and Jacques J. M. van Alphen, Behavioural Ecology & Sociobiology, 42: 1-8 (1998)
This is an experimental test that can be replicated by any competent tropical fishkeeper with half a dozen fish tanks and the requisite perseverance. I cover that paper in much more detail in this document. I think you'll find that document suitably informative.
fluttermoth wrote:
I've always wondered; what is it about long tails that is so attractive? Does anyone know? Long tails seem almost ubiquitous in birds and fish!
fluttermoth wrote:There are two very closely related species of aquarium fish; the platy and the swordtail. Only the male swordtails have a longer tail, but female platies far prefer them to their own males, who have short tails, to the extent that I've been told that ALL platies in the aquarium trade are now platy/swordtail hybrids. So, female platies clearly have a preference for long tails, even though long tails don't occur in their own species.
fluttermoth wrote:Is the 'conspicuous handicap' hypothesis an adequate explanation for such a wide range of examples, and how could a preference evolve before the characteristic and the mutations for it?
Oh, by the way, if you want an example of a test of sexual selection that you yourself can perform in your own home, ...
THWOTH wrote:The mode of the creationist shows scant regard for things like facts, evidence or honestly representing information.[Reveal] Spoiler:One of their main argumentative tactics involves promoting the idea that "science invalidates science" in some way.
With that in mind, one can imagine any number of creationist arguments around Mendel, such as:
a) scientists and biology teachers have always told us that evolution operates according to Mendel's strict model of generic inheritance.
b) since the 1970s scientists have understood that the deterministic Mendelian model of inheritance is not how DNA, genes, chromosome, and therefore evolution, actually works.
c) therefore everything you have heard or been taught about Mendel, and how his ideas are supposed to sit at the very foundation of evolution, is not just wrong, but an out-and-out lie.
d) therefore the only possible alternative explanation for life on Earth is 'god did it'.
Just guessing here though.
Spearthrower wrote:
I think it's an interesting hypothesis that may be true in some cases, but my guess for the most prominent reason is simply real estate. If flashing a bit of colour gets the ladies hot in the cheeks, then flashing a bit more of that colour makes the signal more likely to be received.
Calilasseia wrote:
Indeed, this Genus once again illustrates that tidy categories have a habit of being of limited utility in biology. Although classified as distinct species, the members of that Genus are possibly best thought of as an incipient species complex.
Fenrir wrote:Ultimately there is no such thing as a species.
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