SezMe
post-pre-born
I'm not a biologist but I thought this article was interesting. I'd be interested in comments from those more knowledgeable than I.
It doesn't seem controversial to me, especially when you add extinction into the mix as a confounding factor. All it depends on is "soft" niches - so many available ways to live that survival doesn't depend on a particular ability.
I think the controversial part of the hypothesis is the 2 million years per speciation event, regardless of generation time. They're effectively saying that a mosquito will throw up a new species, given geographical isolation, no faster than an elephant. Not sure about this.
I think the controversial part of the hypothesis is the 2 million years per speciation event, regardless of generation time. They're effectively saying that a mosquito will throw up a new species, given geographical isolation, no faster than an elephant. Not sure about this.
I'm not a biologist but I thought this article was interesting. I'd be interested in comments from those more knowledgeable than I.
Is it radical mutation that is the main driving force of evolution? I thought separation of populations within the same species played a leading role. Some S American tortoises found their way to the Galápagos Islands and new species gradually evolved there.That's a nuance I didn't pick up on, but I could see why generation-time wouldn't necessarily make a difference. If mutation rates (here I mean successful, species-defining types of mutations) are relatively slow, then the generation-time would impact the spread of the mutation, but the overall rate could still be the driver - especially if it takes 2 million years for a suite of chance mutations to have a significant impact.
Is it radical mutation that is the main driving force of evolution? I thought separation of populations within the same species played a leading role. Some S American tortoises found their way to the Galápagos Islands and new species gradually evolved there.
The evolution did not require the S American tortoises to await a radical gigantism mutation for the species now on the Galápagos to be formed.
Is it radical mutation that is the main driving force of evolution? I thought separation of populations within the same species played a leading role. Some S American tortoises found their way to the Galápagos Islands and new species gradually evolved there.
The evolution did not require the S American tortoises to await a radical gigantism mutation for the species now on the Galápagos to be formed.
I was wondering the same thing about the same example. Every isolated island a species of tortoise has made it to has seen some variation of gigantism occur
You can separate populations for a billion years, but if the genes don't change they'll still be the same species. Mutations are necessary to drive differentiation between the species. They don't have to be radical individually, but en mass small changes can have profound effects.Craig B said:Is it radical mutation that is the main driving force of evolution? I thought separation of populations within the same species played a leading role.
It's the same thing, isn't it? If we never separate a subgroup, then any neutral or positive mutations permeate the entire population. You still get different species, but they are only different through time, not contemporaries.
However the common wisdom seems to be, the bigger the base population the slower mutations have an effect over the entire population. Islands present a fascinating laboratory for genetic variation because it is highly likely the entire genetic make up of a species is not represented. So in theory mutation and the rise of new species should be a lot faster in such and environment. But if I am reading this article correctly. That is not the case at all.
Lighten up, Dinwar. I didn't say "surprised", I said I found it interesting.People are surprised by this? This was stuff I learned as an undergrad, right along with how to prep fossils and how to identify the various phyla.
So basically the vast majority of DNA changes are little quirks that don't affect the organism, and that a buildup of these is what causes the speciation (DNA is no longer compatible) milestone to occur.
I always thought sexual reproduction, although somewhat controlled (compared to random neutrons & friends) did the vast majority of changes, and that these could build up at the DNA level as well (e.g. you aren't just safely touching some quasi-variables leading to, say, leg length). Sexual reproduction is magnitudes faster in scouring the evolutionary fitness gradient descent space, which is why it itself evolved, leaving "only" chance nuclear or chemical copy error mutation far behind in the dust.
^Dude, you were born taking umbrage.
Interesting, what do you think of this then?
http://creation.com/refuting-evolution-2-chapter-11-argument-evolution-of-sex
Indeed, the program acknowledges that sex has many disadvantages, e.g., only 50 percent of the genes are passed on to an offspring. This means that there is a 50 percent chance of losing a beneficial mutation.
It is an interesting analysis, but I don't think in the way the reporting suggests.
First, we need some kind of definition of a species that makes some sense. None of them do except with respect to our human desire to attach discrete names to things. The whole of life is an evolutionary continuum. We humans can notice a "boundary" at nodes on a branch where gene flow is restricted over time. If the loss of gene flow is dramatic or prolonged enough, then differences that accumulate over time can be sufficient that prevent any renewed gene flow. That can occur through little changes over a long time (genetic drift) or big changes over a short time (natural and/or sexual selection).
We have abundant examples of very rapid diversification in a lineage - adaptive radiations - and they are very well studied on archipelagos. The combination of isolation from parent stock and intense natural selection in the novel environment is a recipe for speciation, and it don't take no 2 million years. (By my count, there are 5 extant endemic bird species on Hawaii, which is estimated to be 500,000 years old).
I suspect what Hedges and his team have encountered is speciation (largely judged indirectly through gross morphological changes apparent in the fossil record) occurring without isolation and/or marked changes in natural selection. In other words, a raccoon today will likely be quite different from its distant descendants, just through the accumulation of random mutations over time. How long does it take for descendants and ancestors to diverge in this way? Sounds like about 2 million years.
If that analysis holds up, it is in fact really cool. To my knowledge, no one has ever suggested that X amount of genetic change = Y likelihood of speciation. Because the great majority of living things do not occur in extreme environments conducive to rapid speciation, a "whole biosphere" analysis would probably result in Hedges' genetic drift over time thing swamping the influence of things like adaptive radiations in the grand scheme of the development of life on Earth.
Part of the problem, as illustrated by chronospecies, is that the term "speciation" isn't precise. It's not a thing, not a process, not really a suite of processes--it's an end result, which can be brought about by any number of processes.marplots said:My suggestion is that the difference between neutral mutation and positive, speciation-causing mutation, isn't necessarily the mutation itself, but the environment as well. In a much-different, high stress environment, a neutral might actually be a positive.
Tricky to determine. The problem is, a LOT of selection is in-utero. A lot of mutations are such that the zygote doesn't survive long enough to get noticed, much less be born. A mutation to the HOX Box can easily prove fatal, as can mutations to key proteins. So we're left with the rather unenviable option of looking at mutation rates in surviving organisms. That said, we can look at unexpressed genes, or genes where mutations CAN survive, to get a sense of this.A neat question, which has likely been addressed by those in the field, but which I don't know the answer to, is whether there is a fixed background to variability/mutation rate, or whether the mutation rate itself is variable and subject to feedback.
So the short answer is we have a few good guesses, but we're working on it.
Radical mutation is not a significant driving force for evolution. The mutations that contribute to evolution have phenotypic effects that are barely perceptible. A population evolves due to the accumulation of barely perceptible changes, all of which originate as de nova mutations that are barely perceptible.Is it radical mutation that is the main driving force of evolution?
thought separation of populations within the same species played a leading role. Some S American tortoises found their way to the Galápagos Islands and new species gradually evolved there.
The evolution did not require the S American tortoises to await a radical gigantism mutation for the species now on the Galápagos to be formed.
Depends on the mutation. Some are barely perceptible. Some are glaringly so. That was a major finding of de Vrise' primrose experiments, and what allowed him to propose the existence of mutations.Darwin123 said:The mutations that contribute to evolution have phenotypic effects that are barely perceptible.
Sorry, no. It states that the rate of evolution is determined by fitness space, which can be related to changes in the environment. In fact, Gould and other PE advocates argued that most organisms will follow the environment they prefer (if possible, over generations), mitigating the effects of the environment on rates of evolution. That's part of stasis.Punctuated equilibrium theory says that the rate of evolution is almost entirely determined by changes in environment.
A common misconception. In fact, most speciation occurs without mass extinctions; mass extinctions account for only a small amount of new speciation. Local and regional effects are less well-understood. There have been six, maybe seven mass extinctions (depends on how you count). Those cannot account for all diversity, or even a significant chunk of it.In fact, evolution occurs mostly after the environment changes catastrophically in a very short time.
So you're taking umbrage to the charge that you're quick to take umbrage? Got it.Not really.
I'd ask what the Sam Hill you're talking about, but the most parsimonious explanation seems to be that you've confused me with someone else (with whom you've also taken umbrage).You just have a bad habit of saying things that are not true,then declaring that you didn't say them when called out on it. Or denying the whole conversation. Whatever; not really interested in another futile conversation laced with insults, and I will not peruse this further.
Nope, I see them as all equally valid concepts, which renders them equally invalid as well.. . . you appear to be saying that morphology is only an indirect indicator of speciation. This can only mean that you subscribe to a strictly genetic or biological species concept, or a combination of the two.
If there is a second person named "The Shrike", you should report them. They are rapidly eroding your credibility. If not, again, I've drawn my conclusion, and this only supports it.I'd ask what the Sam Hill you're talking about, but the most parsimonious explanation seems to be that you've confused me with someone else (with whom you've also taken umbrage).
Common misconception. The reality is that each taxa has specific traits that are diagnostic at each taxonomic level. Certain traits seem to vary most within species, others between species, others between genera, others between families, and so on. It takes years to understand which traits tell you what about each organism. This makes sense, however; higher-order taxa evolved earlier, and therefore SHOULD be identifiable via different markers than lower-order taxa, and different organisms have different responses to selection pressures and statistical genetic issues. My point is, it's not intuitive which characters are important. It requires a fairly intimate knowledge of the taxa in question to understand this.Using a morphospecies approach, the variability in size and bill shape would be enough to identify multiple species within the currently recognized Song Sparrow.
Depends on the mutation. Some are barely perceptible. Some are glaringly so. That was a major finding of de Vrise' primrose experiments, and what allowed him to propose the existence of mutations.
If I saw something report-worthy I would. You're the one claiming habitual lying and pointless, insult-laden conversations courtesy of this brigand. (You're also the one who sent me an angry PM recently that was clearly directed at someone else, so if there's a pattern here maybe it's you confusing the posters with whom you're interacting.)If there is a second person named "The Shrike", you should report them.
Of course, but I think you take this too far. Each taxa diagnostic for each taxonomic level? I think you've indicated in the past that you work with Forams, and I agree that would be the case with them - perhaps tautologically so if test morphology is the primary criterion for classification. Here's an example of the variability I'm talking about within and between two species of congeneric birds. In this case, the comparison is wing length in mm from the wrist to the tip of the longest primary:Common misconception. The reality is that each taxa has specific traits that are diagnostic at each taxonomic level.
I'm with you on the Mammalia. Re: bird bills - I might agree, but can you clarify what you mean by important in your context? Important for what?I would be astonished, however, to find that variability in bill shape is so important. I'm not entirely convinced that dental variability is as critical as often portrayed in Mammalia.
Hey, this all sounds familiar. Maybe you don't take umbrage with my position after all . . .The issue is, "species" do not, as such, exist in the wild. The concept of a species is a human-made construct that assists in understanding biology. What exists in biology are populations. . . . As such, I see no reason to assume one species concept is inherently superior to any other--
Wait, is that what that means? I'm not sure. This is where I need to read the paper and get a better idea of what they did. My gut tells me that they should have only included in their analysis examples using ONE strictly applied species concept, rather than jumble them all together which is what it superficially appears they did. You don't have any problem with them running the analysis on examples that applied different species concepts?. . . and that means that we can move between them as needed without any hesitation, so long as we acknowledge the limitations of each concept.
Very cool, but the thing that's on me is only in the context of this paper and the methods they used to obtain what might be a really provocative result. Again, I'd be a lot more comfortable about interpreting the analysis if they only used osteological evidence and only applied a morphospecies concept. Your experience tells you that I'm being too rigid and that my concerns over source material and different species concepts are red herrings in this context. Correct?I will say that limiting yourself to osteological evidence is on you, not paleontology. We work with squishy bits quite frequently.
Actually, I'm vert paleo these days. I merely know folks who work with forams, and am reporting what they've told me. I've seen enough data to agree with their conclusions, but am not an expert.The Shrike said:I think you've indicated in the past that you work with Forams
I'm not sure how this CAN be taken too far. What I mean is, in Decapoda, there are certain traits that differentiate between the various suborders and families. Within, say, Brachyura, there are DIFFERENT traits that differentiate between THOSE sub-groups. Within Raninoida, there are DIFFERENT traits that differetiate between THOSE sub-groups. All of these traits are found in each species--a Raninid has all the traits of Brachyura and Decapoda--and it takes a fair amount of expertise to differentiate between them.Of course, but I think you take this too far. Each taxa diagnostic for each taxonomic level?
I think we can agree that there's a gulf of difference between "we can move between them as needed without any hesitation, so long as we acknowledge the limitations of each concept" and "jumble them all together". Jumbling things all together rather indicates that one has not properly acknowledged the limitations of each concept.Wait, is that what that means? I'm not sure. This is where I need to read the paper and get a better idea of what they did. My gut tells me that they should have only included in their analysis examples using ONE strictly applied species concept, rather than jumble them all together which is what it superficially appears they did.
Depends on how they do it, but fundamentally, no. I CAN'T have such a problem. No one who works with cladograms that include both extant and extinct taxa can. When you do phylogenies that include extinct and extant species, this happens all the time. There are methods to address the issues that arise from such mixtures of methods, and obviously great caution must be exercised, but it's standard procedure anymore.You don't have any problem with them running the analysis on examples that applied different species concepts?
I don't know enough about the species in question to know if the example is valid, but I suspect that there are more differences than merely the beak length. I may be wrong, but in most of the cases I've seen that's been the case. Even when working with just skulls and teeth--even when just working with teeth--there are multiple characters involved.So here is an example - and I'm sure you can think of many more of these than I can - in which a morphospecies concept is limiting, just as there are limitations in applying genetic and biological species concepts.