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GP on the Origin of Body Plans [OoBP] challenge

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. . . here (at 194) in his amazing engineering thread as he responds to Dionisio:

>>Dionisio:

Thank you for summarizing that interesting discussion.

I will summarize it even more.

1) Nobody knows how morphogenesis is controlled and guided.

2) Moran is no exception to that.

3) “Experts” are no exception to that.

4) However, according to Moran (and, unfortunately, he is probably quite right): “experts do not see a need to encode body plans and brain in our genome”

5) You and I, and probably some more sensible people, do see that need.

6) So, it seems, the problem is not about what we know, but about what we see as a need.

Now, I notice that Moran says:

“experts do not see a need to encode body plans and brain in our genome” (emphasis mine)

OK, that can mean two very different things:

a) Experts do not see a need to encode body plans and brain in our genome, but they think that body plans and the brain are encoded elsewhere

OR

b) Experts do not see a need to encode body plans and brain anywhere.

I will not ask Moran what he really meant, because I think it unlikely that he would respond. So, I can only guess.

I would say that he means b). Why? Because, if he means a), I could probably partially agree, and that is a rather unlikely situation, IMO.

Now, a) just means that the procedures are encoded elsewhere. That is probably true, at least in part. That “elsewhere can still mean two different things:

a1) At some epigenetic level, that we can imagine

a2) In some other way, that at present we cannot even imagine

Well, I believe that all of that is true. The procedures are encoded in the genome, both at the level of proteome (see my OP here, for that) and at the level of non coding DNA (Ouch! Moran will not like that). And they are also encoded at many epigenetic levels. And they are also encoded at other levels that at present we cannot imagine.

But there is one certainty, for me: they are encoded somewhere.

Because, you see, most neo darwinists would rather go with b): they really believe that those things are not encoded anywhere.

Now, while you and I certainly find that idea completely absurd, let’s try to understand what they think.

The best, and most honest, admission about that, in my memory, was made by Piotr, some time ago, in a discussion that was exactly about the procedures for cell (and tissue, and organ, and body) development. He said, if I remember well:

“I think it’s just the memory of what worked”.

OK, that’s a very honest statement of a neo darwinian perspective. But, as it is honest, it includes a precious little word: memory.

Now, you and I, having some love for informatics and programming, know all too well that “memory” is not a vague concept.

Memory of information must be stored to survive and be available. And that requires, in our human experience, some storage medium. Usually some physical (and often expensive) storage medium.

IOWs, no memory storage medium, no party.

So, I would like to ask Piotr (if he still reads this blog, that is unlikely), or Moran (if he likes to answer, that is unlikely), or anyone else:

Where and how are the procedure for cell (and tissue, and organ, and body) development stored?

Because, you see, they are certainly available in some way, otherwise how could the embryo of any organism generate the full body?

I suppose that the most likely argument of any neo darwinist, at this point, would be that those procedures must, after all, be very simple. A few HARs, a few hundred, at best a few thousand, nucleotides, and the deed is done.

Done? The human body plan? The human brain and nervous system? The whole immunology network? And so on, and so on?

You and I, having some love for informatics and programming, know all too well a very basic truth: very simple programs require some limited memory to be stored, but very complex programs require a lot of memory.

So, is the information for human brain really so simple? Is it like squeezing, say, Windows 10 in 1-2 KB at most?

OK, we know that the biological designer must be very good, but so good?

Ah, but I forgot: neo darwinian evolution can do practically anything: even miracles, provided we don’t call them miracles! >>

He goes on, in 201:

>>By the way, let’s comment some more on this interesting issue of development, always in the light of the results presented in this OP.

Vertebrates are considered as a subphylum of chordates: chordates with backbones.

So, in a sense, the basic body plan is set up in chordates, with the appearance of the notochord, and other features.

As we know, phyla correspond to basic body plans. But, strangely enough, they all appear very “suddenly”, during the so called “Cambrian explosion” (approximately 541 – 520 million years ago).

We know well all the debates about that amazing event. Of course, neo darwinist have tried their best to hypothesize that the explosion is not an explosion at all, and that the true information for all those new body plans was being “manufactured” more gradually during the previous times. And so on.

But the evidence of the fossils remains what it is, and I don’t think that our “polite dissenters” have succeeded in explaining away the “almost miracle” of the Cambrian events.

However, with vertebrates we are apparently observing an event slightly later than the Cambrian explosion itself. The emergence of a very important (for future developments) subphylum in the well established phylum of chordata.

That allows to localize better the emergence of the new information, to somewhat later than the Cambrian, but anyway well more than 400 million years ago.

Now, if we judge from the following natural history, it seems that the emergence of vertebrates was a very successful innovation: indeed, chordates not vertebrates are a rather small bunch of organisms today, while vertebrates are, in comparison, one of the main representative groups of animals, from many points of view, even if we don’t consider the side aspect that we, as humans, are part of it.

So, it is rather interesting to observe, according to the data presented in the OP, that the transition to vertebrates was a very exceptional “jump” from the point of view of some specific functional information in the proteome, certainly the biggest step we can observe in the accumulation of human conserved protein information. In that sense, it is a much bigger step than the simple appearance of the phylum chordata, with the appearence of more than twice human conserved information (3,708,977 bits vs 1,685,550, not corrected for redundancy).

If we want to make hypotheses about that interesting fact, we could probably reason that the new body plan of vertebrates includes at least two major innovations that will be very important in all the future natural history of that branch:

1) Cephalization, and in particular the gradual development of the brain, and therefore of all new functiona connected to that

2) Adaptive immunity, which appears for the first time in jawed vertebrates.

Both these innovations have a common denominator: they are linked to the appearance and development of two very complex regulatory systems, both aimed to a very complex and nuanced interaction with the outer environment.

IOWs, they are both, in different ways, complex systems that process information from the outer world.

That is an important concept, because it bears a fundamental implication:

If the bulk of the huge informational jump that appears in the vertebrate proteome is really linked to the premises for the development of the central nervous system and the brain and of the adaptive immune system, then it is perfectly reasonable to think that much of that new information must be strongly connected, as one can expect in any big and complex system that mainly processes information and reacts to it in very complex and nuanced modalities.

Another way to say it is that, in that huge informational jump, a great part of the total information can be expected to be irreducibly complex.>>

Sobering issues, well worth headlining and inviting further discussion. Let’s see if objectors to design thought have a good, cogent and plausible counter-case that is suitably empirically well-grounded in actual observations rather than ideologically loadesd reconstructions of the inherently unobservable remote past of origins. END

PS: I have been very busy RW.

Comments
Dionisio @ 28: Yeah, RVB8 is far well too documented by now and I've spent too much time debating in some of the dumbest places on the internet for me to not know better. A bit foolish of me to try squeezing blood from a turnip. Thanks for the consideration. RVB8: If you wish to retreat from a challenge for specifics to a vacuous literary polemic, I really feel no need or point to giving chase. Should you ever decide on a proper argument, I would gladly engage you at that point.LocalMinimum
April 3, 2017
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GPuccio - I'm not sure how much of the scientific literature you've read, but I think you should read it more carefully. You write
Of course, there are also maternal (or other) epigenetic components, and personally I think that much is to be found, probably in unsuspected forms, in non coding DNA.
but we already know this - a major theme of Endless Forms Most Beautiful, and indeed the evo-devo revolution, is that a lot of evolution in development is due to changes in the control of gene expression (i.e. epigenetics is involved, in one form or another).Bob O'H
April 3, 2017
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Bob O'H: Thank you for your very balanced intervention. No, I have not read that book, but I read much of what is published in the scientific literature, because I am very interested in this field. I don't agree that "my argument in the OP is largely from ignorance". I think it is a reasonable way to ask questions about what we observe. However, you are obviously entitled to your opinion. You say: "what is (mostly*) encoded in our genes is the process to produce a body plan, not the plan itself" I can agree. But frankly, I can't see the difference. A plan is the recording of the procedures to obtain a final result. I can agree that we will not find in the genome something like the "homunculus" we find in the cerebral cortex, but still we have to find there all the detailed and complex information that controls and guides the process to the end. And I don't thing that it will be all in the protein coding genes, although I have tried to argue here that some relevant part of it is there, and is often underestimated, Please, read my post #47 here for that. Of course, there are also maternal (or other) epigenetic components, and personally I think that much is to be found, probably in unsuspected forms, in non coding DNA. But you will probably think differently about that. Finally, I would really like to know if you have read my OP from which this OP is derived: https://uncommondescent.com/intelligent-design/the-amazing-level-of-engineering-in-the-transition-to-the-vertebrate-proteome-a-global-analysis/ I would really like to know what you think about that. If you like to tell.gpuccio
April 3, 2017
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KF, Dionisio: In my post #54 at the other thread: https://uncommondescent.com/intelligent-design/the-amazing-level-of-engineering-in-the-transition-to-the-vertebrate-proteome-a-global-analysis/#comment-627591 I wrote: "Transcription factors are a good example: the DNA binding domain is usually the most conserved part of the molecule. But TFs do not simply interact with DNA: they interact with one another, often in complex cumulative structures, and with other molecules and biochemical pathways. That part, the “regulatory” part, that in the end determines what the TF bound to DNA will do, is much less understood, and often less conserved, probably because it is functionally tweaked to different final functions." I think it can be interesting to offer an example of that here, because it can show the point that specific changes in the existing proteome can have great importnace in new body plans, and happen in jumps. So, let's take Pax-6, an important transcription factor active during embryonic development, which is so quoted in the Wikipedia page so kindly linked by rvb8:
The field is characterised by some key concepts, which took biologists by surprise. One is deep homology, the finding that dissimilar organs such as the eyes of insects, vertebrates and cephalopod molluscs, long thought to have evolved separately, are controlled by similar genes such as pax-6, from the evo-devo gene toolkit. These genes are ancient, being highly conserved among phyla; they generate the patterns in time and space which shape the embryo, and ultimately form the body plan of the organism.
True. But let's take a more detailed look to this important TF using the concept of Human Conserved Information (from now on, HCI), developed in my OP. The functional density (per aminoacid site) of HCI in PAX-6 is as follows: Cnidaria: 0.7393365 Cephalopoda: 1.21564 Deuterostomia (not vertebrates): 1.232227 (jump here) Cartilaginous fish: 1.966825 Bony fish: 2.007109 Amphibia: 2.035545 Crocodylia: 2.052133 Marsupialia: 2.033175 Afrotheria: 2.061611 As everybody can see, while the protein has a very good homology with the human form already in protostomia (1.21 baa in Cephalopoda), there is a sudden and important jump in cartilaginous fish, of: 0.7345972 baa That jump is obviosuly linked to the new vertebrate body plan. Moreover, the density of HCI in cartilaginous fish reaches almost its maximum value (remember, 2,2 baa is the value for identity), and remains rather constant up to mammals and humans. Now, let's try to understand in detail what happens. I have blasted the human protein against Drosophila melanogaster (fruit fly, a Protostome) and Callorhincus milii (a shark, Cartilaginous fish). Well, as expected, the homology is: Drosophila: 435 bits, 52% identities, 1.030805 baa Callorhincus: 830 bits, 95% identities, 1.966824 baa Here, again, the jump is conspicuous. But the interesting thing is: what changes? If we look at the blast, it is i,,ediately obvious that the homology found in Drosophila (or, say, in all protostomia and non vertebrate dueterostomia) is strictly confined to two well defined regions of the sequence: 1) The Paired Box domain (AAs 4 - 128) 2) The Homeobox domain (AAs 211 - 266) Both are DNA binding domains. Together, they are responsible for the about 50% identity, slightly more than 400 bits homology, slightly more than 1 baa, that we find between pre-vertebrates and humans. IOWs, the basci homology of PAX-6 in pre-vertebrates with the human protein is almost entirely attributable to the two recognizable DNA binding domains, which are both highly conserved. But what about the rest of the sequence? PAX-6 is 422 AAs long. The two domains, together, are less than 200 AAs. And the rest? The rest is essentially made of two parts: a) A segment of slightly more than 50 AAs, between the two domains. b) The C-terminal part of the molecule, about 150 AAs long. Well, the interesting point is: These two parts of the molecule (not corresponding to recognizable domains), when compared to the human protein, are almost completely different in Drosophila (and, in general, in pre-vertebrates), while they are almost identical already in Cartilaginous fish, and so they remain, almost unchanged, throughout the following natural evolutionary history (more than 400 million years). So, not only a big jump, but a very specific, targeted jump. Just as a check, I will paste here again my statement from my other thread, that was the starting point for this post:
Transcription factors are a good example: the DNA binding domain is usually the most conserved part of the molecule. But TFs do not simply interact with DNA: they interact with one another, often in complex cumulative structures, and with other molecules and biochemical pathways. That part, the “regulatory” part, that in the end determines what the TF bound to DNA will do, is much less understood, and often less conserved, probably because it is functionally tweaked to different final functions.
What do you think? Am I right here?gpuccio
April 3, 2017
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gpuccio: Your example on the use and meaning of the words 'controlled' and 'guided' vs. the word 'implemented' is an excellent illustration I may refer to in future discussions.Dionisio
April 3, 2017
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gpuccio @ 29 - the questions you raise are important ones, and are central to developmental genetics. So, I'm curious to know - have you read much about that area? I found Endless Forms Most Beautiful helpful in explaining how cell differentiation is controlled. It's not a simple process, I'm afraid, but we actually do have a lot of knowledge about it ("we", BTW, means scientists and humanity, not including me specifically). Your argument in the OP is largely from ignorance. I can't comment on what Larry Moran meant (partly because I'm too lazy to try to find the original quote), but what is (mostly*) encoded in our genes is the process to produce a body plan, not the plan itself. * 'mostly' because there are also maternal factors in play too, i.e. the mother provides some of the information for development to occur correctly. As with most of biology, it's more complicated than we'd wish.Bob O'H
April 3, 2017
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gpuccio @41:
By the way, did you notice that the Wikipedia article says: “at exactly the right times and in exactly the right places” using “exactly” not once but twice, without even bolding it? Tricky article that it is!
Tricky? That's how we call it, but the distinguished Canadian biochemistry professor would call it dishonest article! :) According to his criteria, the referenced article proves that Wikipedia doesn't have honest articles!Dionisio
April 3, 2017
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gpuccio: Ah, it's fun to argue with "l'italiano vero"! :) BTW, I'm not a teenager either. This modern lack of attention to details and word meaning is annoying. But perhaps you're right when you said that words should be bolder in the questions. :)Dionisio
April 3, 2017
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Dionisio: "That seems old fashioned." Well, I am not exactly (!) a teenager.gpuccio
April 3, 2017
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Dionisio: Ah, words! I love them. :) By the way, did you notice that the Wikipedia article says: "at exactly the right times and in exactly the right places" using "exactly" not once but twice, without even bolding it? Tricky article that it is! :)gpuccio
April 3, 2017
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gpuccio @29:
Please, note that I have said: “Nobody knows how morphogenesis is controlled and guided.” Not: Nobody knows how morphogenesis is implemented.
C'mon doctor, I can see you're 'picky' about the contextual meaning of different words. :) That seems old fashioned. These days many people don't pay that kind of careful attention to words and meanings. :)Dionisio
April 3, 2017
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Dionisio: Maybe the jellyfish has escaped... :)gpuccio
April 3, 2017
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rvb8: "I can’t answer your in depth reply." Well, that's a honest admission, at least. Thank you. "take these brilliant insights to a wider audience " I think they are public enough here. However, thank you for the kind suggestion. :)gpuccio
April 3, 2017
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KF: Wonderful point about switches. Switches are, definitely, the best tool for the old three-card trick. Just an example: We know well that overexpression of just 4 TFs, Oct4, Sox2, Klf4 and c-Myc, can induce pluripotent stem cells from differentiated fibroblasts. Indeed, even simpler cocktails can do that. A miracle? Does that mean that we understand how pluripotent stem cells work? Does that mean that we understand the process of differentiation or de-differentiation? No and no. Not at all. Those are switches. Wonderful, powerful, elegant switches. In a sense, a switch that lights a lamp can be the same as a switch that turns on a computer. Same complexity in the switch, but some small difference in the circuit! :)gpuccio
April 3, 2017
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gpuccio, Dionisio, I can't answer your in depth reply. As said, take these brilliant insights to a wider audience at say Pandas, WEIT, or the more friendly TSZ. Let them be eviscerated there.rvb8
April 3, 2017
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GP, it is often a feature of communication-based and cybernetic systems that they contain switches, short/ small, seemingly simple components that redirect complex processes down alternative paths. I think of the not function in logic, or of mode bits in assembly languages, or of comparators [or subtractors or differencing amplifiers) in control loops, or even of word shifts like "moral" vs "amoral" vs again something like "non-moral." But to focus on the switch misses the key: for the alternative pathways to exist, they have to each be present, nodes that trigger modified pathways do not remove the need for valid pathways to be present. If a similar switch element triggers compound vs mammalian eye development, that does not change the differing and astonishingly precise information and process requisites for both. Optical systems often require surfaces set up correctly to order a fraction of the wavelength of light; and here there are significant architectural differences and even strategies. The issue of Hox genes pops up just as a term. When an eye is to be built into an organism, too, it does not stand on its own: skeletal structure, nerve paths and brain structures to process the notoriously wide bandwidth information involved with video come into play. There have to be wider issues on what to do with visual info, as in: that's a cat there, run. Pattern recognition in real time and appropriate rapid responsiveness, etc. The wings of various animals come to mind also: a wing is already a complex aerodynamic entity, and it needs muscles, power flows, control, etc to work. And much more. KFkairosfocus
April 3, 2017
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mike1962: Thank you for the very kind words. "Write a book" Maybe, maybe...gpuccio
April 3, 2017
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Dionisio: "Did I understand this right?" Yes! "I think GP is cooking a delicious meal for thoughts." Thank you. That's probably the only kind of thing I can cook! :) "Despite some noise in the environment, caused by jellyfish that got trapped in the net." Maybe a jellyfish is better than nothing! :)gpuccio
April 3, 2017
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KF, I think GP is cooking a delicious meal for thoughts. Despite some noise in the environment, caused by jellyfish that got trapped in the net. :) Let's stay tuned. GP's comments are keeping me at the edge of the seat. :)Dionisio
April 3, 2017
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gpuccio, Excellent explanation! Are you saying that at this point scientists can describe many processes right as they are observed, but that doesn't tell us much about how exactly all those biological shows are managed and where are the scripts for all the actors and the choreographies kept stored, so that they are easily accessible when needed? Could it be compared to someone going to a theatre and seeing a beautiful ballet performance, then later being able to describe the whole show in many details, but not knowing how exactly that show was managed or directed and not having any idea where the documents containing the choreographies are stored? Note that in the case of how the actual management processes occur they may have some clues or hints, though perhaps many times vague or blurred. But much less is known about the location where the procedures are stored and the format they are stored in. Did I understand this right? Thanks. PS. I still want to read your comment mere carefully. It's possible will have more questions.Dionisio
April 3, 2017
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rvb8: The Wikipedia article you point to is a very good example of the ideological bias I have described in post #29. We learn that:
Among the more surprising and, perhaps, counterintuitive (from a neo-Darwinian viewpoint) results of recent research in evolutionary developmental biology is that the diversity of body plans and morphology in organisms across many phyla are not necessarily reflected in diversity at the level of the sequences of genes, including those of the developmental genetic toolkit and other genes involved in development. Indeed, as Gerhart and Kirschner have noted, there is an apparent paradox: "where we most expect to find variation, we find conservation, a lack of change".[43] So, if the observed morphological novelty between different clades does not come from changes in gene sequences (such as by mutation), where does it come from? Novelty may arise by mutation-driven changes in gene regulation.
OK. But my OP here: https://uncommondescent.com/intelligent-design/the-amazing-level-of-engineering-in-the-transition-to-the-vertebrate-proteome-a-global-analysis/ is about the huge modfications that have to occur in the proteome too, so that gene regulation may be different. That is an important point, often underestimated in current biological thinking. And:
The protein products of the regulatory toolkit are reused not by duplication and modification, but by a complex mosaic of pleiotropy, being applied unchanged in many independent developmental processes, giving pattern to many dissimilar body structures.[36] The loci of these pleiotropic toolkit genes have large, complicated and modular cis-regulatory elements. For example, while a non-pleiotropic rhodopsin gene in the fruit fly has a cis-regulatory element just a few hundred base pairs long, the pleiotropic eyeless cis-regulatory region contains 6 cis-regulatory elements in over 7000 base pairs.[36] The regulatory networks involved are often very large. Each regulatory protein controls "scores to hundreds" of cis-regulatory elements. For instance, 67 fruit fly transcription factors controlled on average 124 target genes each.[36] All this complexity enables genes involved in the development of the embryo to be switched on and off at exactly the right times and in exactly the right places. Some of these genes are structural, directly forming enzymes, tissues and organs of the embryo. But many others are themselves regulatory genes, so what is switched on is often a precisely-timed cascade of switching, involving turning on one developmental process after another in the developing embryo.[36]
Emphasis mine. OK, That seems a fine passage. Merely descriptive again, but at least it admits the complexity of the whole. But then, just a few vague words about "The origin of novelty", and in particular this jewel:
Given that small changes in toolbox genes can cause significant changes in body structures, they have often enabled the same function convergently or in parallel.
Emphasis mine. ??????? Wait a moment, what does that mean? All that talk about "all this complexity", and "large, complicated and modular cis-regulatory elements", and all they can say is that: "small changes in toolbox genes can cause significant changes in body structures"? So, the idea is simple and elegant: I just change a couple of aminoacids in a transcription factor and look: Before: it interacted with 1000 other modular components so that it generated the eye in drosophila. After. it interacts with some other 1000 modular components, so that it generate the eye in the mouse. Perfect! Everybody can see how a very small change (no real complex functional information implied) has implement an apparently complex result. That procedure is so simple, that it has certainly "often enabled the same function convergently or in parallel". Where's the problem? Well, for myself, I definitely feel fooled. Like in the old three-card trick. A simple and elegant trick, but a trick just the same. Anybody else feels fooled, like me? :)gpuccio
April 3, 2017
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Dionisio: OK, it's a very hard statement. But maybe I will retain it. Please, note that I have said: "Nobody knows how morphogenesis is controlled and guided." Not: Nobody knows how morphogenesis is implemented. IOWs, we certainly know a lot about pathways that are implied in morphogenesis. For example, we know that in many steps there is a role for some morphogens. But, as you have kindly reminded to Moran and to us, how is a morphogen gradient generated in each specific case? IOWs, what initiates, controls and guides the generation of a specific morphogen gradient in each specific context? My impression is that all knowledge we have about morphogenesis is descriptive: OK, we see that when a cell differentiates in this way this and that happen. But my question is different: What kind of information is necessary in a cell so that it can differentiate along some pathway or some other pathway in different conditions? I will try to be even more clear with a generic example. Let's say that we have a simple multicellular organism A where a cell "a" generates 30 cells that are all similar: aaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa. That's all, in the development of that organism. Now, let's say that from that organism derives a more complex, but still rather simple, multicellular organism B where an original cell "b" generates three different layers of cells, each with very different features and functionalities, and specific spatial arrangements: ccccccccccddddddddddeeeeeeeeee OK, now let's say that the second organism B derives, by common descent, from the older organism A. Now, the simple question is: What has to change in the original cell "a" so that it becomes the new original cell "b", with the new potential to generate three different types of cells? Whatever it is, that is exactly the information necessary for the cell differentiation that we observe in the organism B, and that was not present in organism A. That information must exist, and must be, in principle, quantifiable. It must include not only the effectors (proteins like transcription factors, promoters, enhancers, epigenetic tools, and so on), but also the specific configuration of those effectors, and very likely of other components that we still don't understand, that initiate, control and guide the processes we observe. That's what I call the functional information linked to the procedure. Because, of course, if I need to make a specific change to something to generate a new functionality in that object, what I am doing is simply that: I am adding functional information. Each change that is necessary to implement a new functionality is functional information linked to that function Now, the myth of darwinists is that such "functional information linked to the procedures" may be very simple. They believe, with the simple and sometimes aggressive faith of a new enthusiastic religious adept, that certainly a few small changes here and there, some of them still elusive, are able to make an embryo generate "simple" new objects like a liver cell, or T and B lymphocytes, or "simple" structure like the kidney and the brain. After all, what's all the fuss about? Neo-darwinian evolution can do almost-miracles like OOL, why should it be afraid to try cell, tissue, organ and body plan development? The important point is not to connect too much new information to that, because those tricky creationists, camouflaged as IDists, are proud enough of the functional information they already see in known proteins, and we certainly don't want to give them further ammunition! :)gpuccio
April 2, 2017
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LocalMinimum @23: I see your valid point, but you may want to consider not taking that senseless post @22 seriously. Save your precious time for better things. Don't squander it.Dionisio
April 2, 2017
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LocalM, No! If you can't, or won't read it I can't and won't make you. But these two parts are full of links you can and, no doubt with the curiosity inherrant in ID folk, will ignore. 2.)The control of body structure. 3.)The origins of novelty. The two other scientists and their books that I mention, you should also avoid, being full of facts, and research etc. You should keep reading Jonathan Wells's earth shattering 'Icons of Evolution'. To be followed by 'More Icons of Evolution', and most recently 'Zombie Science: More Icons of Evolution'. (Zombie Science? Really? This man who is perrenially ignored, is getting annoyed and irritated, and it shows in this childish tantrum title.) Perhaps in a few years we'll get, 'Icons 3', maybe 'Icons Rebooted'. Seriously? Talk about flogging a dead horse. I leave it to Christopher Hitchens to describe the impact on science of this man and these tomes; "Mr Wells's book is unlikely to merit even a footnote in the history of piffle." The man was indeed a word smith. Dionosio, no I made a mistake. It shoud be one 'l'. I don't mind admitting my errors and failures in syntax and style; you?rvb8
April 2, 2017
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KF, Sorry, the jellyfish (@22) got in the net. Please, would you mind removing it so that it leaves room for better quality fish? :)Dionisio
April 2, 2017
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@22:
The article on, ‘Evollutionary development biology’,in Wikipedia would be a convenient non-threatening place [...]
Does the word "evollution" (with double 'L') refer to the Neo-Darwinian stuff? Do they write it with double 'L' to indicate that it's wrong or that it doesn't exist? :)Dionisio
April 2, 2017
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rvb8 at #22: Is that an attempt at "discussion"? Because, you know, it really doesn't look that way. Not at all. Maybe you are only trying to remind us that you exist. OK, you exist. But are you capable of personal thinking, ideas, intellectual confrontation, debate, and similar human activities? Just to know...gpuccio
April 2, 2017
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RVB8: The article on, ‘Evollutionary[sic] development biology’,in Wikipedia would be a convenient non-threatening place for you ostriches to start with. Again, you won’t like it. It’s full of clear evidence based theories, with elegant hypotheses explaining likely routes, and even predictive possible futures.
What I see is what would be a decent little blurb on developmental biology, padded out with pretty standard and not particularly inspiring or useful evolutionary speculation. Could you explain precisely what it is that I should be finding here? Perhaps list the best/strongest examples of your statement?LocalMinimum
April 2, 2017
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The article on, 'Evollutionary development biology',in Wikipedia would be a convenient non-threatening place for you ostriches to start with. Again, you won't like it. It's full of clear evidence based theories, with elegant hypotheses explaining likely routes, and even predictive possible futures. The chapters 5, 'Getting a Head'; 6, 'The Best-Laid (Body) Plans; and 7, 'Adventures in Bodybuilding', from Neil Shubin's 'Your Inner Fish', could also be of use for understanding where CURRENT research is at, on this question. Also Coyne's 'WEIT', chapter 3, 'Remnants: Vestiges, Embryos, and Bad Design', also delves into body plans, and their building. Feel free however to declare the non-argument won, and to watch the clouds float over that very deep well you find youselves in. Dionosio, the silence eminates from the ID side. With Irreducible Complexity, and Specified Complexity, (along of course, with the utterly unknown non-concept, FSCO/I), the only partially defined (with zero experimentation, and evidence) ideas, it is ID that is home to those crickets.rvb8
April 2, 2017
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gpuccio wrote:
Nobody knows how morphogenesis is controlled and guided.
That's a very hard statement. I'll soften it a little: Biologists do know something about it, but what is known points doubtlessly to intelligent design. What will be revealed tomorrow will keep pointing in that direction, even more. No objections out there? ...deafening silence… Hello! Anybody out there? ...crickets chirp...Dionisio
April 2, 2017
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