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Originally posted by mattison0922
Originally posted by soficrow
Okay - this isn't really on topic, and I just scanned only the first post.
BUT - the examples in the first post all fit with what might be described as "fractal design."
Sofi, your example escapes me. I can't for the life of me come up with a way that a biological rotary motor can be considered a fractal. Can please elaborate? Thanks.
Originally posted by soficrow
Okay. I could be full of it on this one - but - I scanned the bits about jaws and hinges, then ball and sockets - both organic, biological. Relevant background to me is that inventors seem usually to copy from life, and simply translate into non-living mechanical.
Anyway - the jaw and hinges/ball and socket examples made me think of faces and joints - and fractals. ...There is a hypothesis that complex organisms like animals really are just composites of microbes - again, fractals - what happens/forms in the minute particular are reflected in the macro.
...Not a 'position' I can defend. Just a leap. And that's how I got there, more or less.
Originally posted by mattison0922
Sofi, thanks for the clarification. I understand your point. I think your argument is reasonable, but it is not really in conflict with IDT. IDT doesn't have a problem with the idea of 'common descent,' which is what I think you were going for with the fractals thing.
So the fractal analogy is somewhat reasonable right down the the level of single cell. Below this level is where the 'fractal equation' breaks down.
In essence this is why IDT has come about. Thus far, there is not a reasonable naturlistic law, phenomena, theory, or otherwise that can account for the formation of the first fractal.
Now I am going to comment on something I don't really know much about, But in essence isn't the fractal argument and argument from an ID perspective?
Certainly the fractal is a repeat of some mathematical expression, that continues from the 'micro' to 'macro' scales, but the ultimate source of that fractal equation is based on an intelligent source, ie; the individual that derived or input or whatever is done with equation. So while the fractal is in fact a repeated pattern, is it not derived from sort sort of intelligence, or is it a consequence of some mathematical law?
Originally posted by soficrow
Are you sure? (I don't know, but it seems the info above may suggest otherwise.)
That may be. On the surface, I have no problem with accepting the notion of an "over intelligence" - described as a God, or as an evolved cohesion, or any of several other descriptions.
Maybe the original fractal IS God - but if so, who created her?
And BTW - if an intelligence is responsible for the first fractal, then offering to postulate a mathematical law as an opposing argument does not work IMO.
Originally posted by Zipdot
Hoo boy... There's a lot to talk about here... I don't know where to begin.
I liked the idea of "irreducible complexity" the first time around, when it was predicted by evolution supporter Hermann J. Muller in 1939 and called "interlocking complexity." (Source)
We're currently exploring the possible step by step evolution of complex biochemical pathways. It's a work in progress. However, we're not ready to throw our hands up and say "Ya got me. It must be DESIGNED that way. Yeah," and then wipe our sweatty brows.
It may appear that evolutionary theory "breaks down" in microbiological examination, but I believe that what we're really seeing is a simple lag period between discovery and explanation.
As an FSME, I am attempting a campaign for cohesiveness, which I think has largely been achieved. More and more, in our forum, we are seeing concessions and willingness to accept alternative ideas.
Originally posted by soficrow
Okay - this isn't really on topic, and I just scanned only the first post.
BUT - the examples in the first post all fit with what might be described as "fractal design."
burgeoning field of research in DNA science involves attempts to understand the self- assembly capabilities of complex biological molecules such as proteins and DNA by producing synthetic molecules that form periodic or aperiodic crystals, thereby demonstrating the propensity for such synthetic molecules to bind together in predictable ways. Recently, such experiments have been combined with prefatory computer simulations to produce more complex fractal aperiodic crystals based on synthetic molecules, and although the results are interesting, it is noteworthy that the self-assembling biological molecules being so 'modeled' are assumed to have evolved by Darwinian mechanisms - despite the probabilistic prohibitions of such a process occurring - and that little reference is made to the likelihood of complex self assembly capabilities arising by such mechanisms ...(more)
Using DNA configured abstract Wang tiles in xgrow simulation software with the kinetic tile assembly model, researchers Paul Rothemind et. al have attempted to begin to gain an insight into the principles behind the rules for biochemical self assembly by generating Sierpinski Triangles with DNA binding rules computationally, and producing amazing rezults in-vitro with fractal crystal grow guided by the simulated tile configurations. This fascinating work incorporates some astonishing observations and conclusions (with actual Sierpinski Triangle fractal patterns produced in crystals in- vitro) but may demonstrate some of the hallmark problems with using in-silica simulations to draw conclusions about biochemical/biological systems, in that CSI is assumed to be the product of chance based evolution, and the methodology and experimental-simulative procedures involve the induction and imposition of externally imputed rules and parameters for cellular automata in order to obtain desired results, which are then reflected in-vitro...(more)
www.iscid.org...
benito (Mar 25, 2004 9:18:59 PM)
i read your book Treasures and i am amazed at the complexity and order inherent in the patterns. Unlike the monsters of the Mandelbrot set, the natural patterns of those of order and suggest an underlying design. What do you think underpins the order and complexity of such design: is there a Design in the designs we see?
carlos puente (Mar 25, 2004 9:22:46 PM)
Thanks benito, the object one gets via these ideas certainly evoke those in the Mandelbrot set, but these ones turn out not be fractal, for if one looks inside at increased resolutions one would not find additional structure. The objects are indeed mathematical designs, for once a trail of iterations is set one always finds them. The order one sees is rather lovely and at the same time mysterious for it depends in a non trivial manner on the actual iterations.
J. Nelse (Mar 25, 2004 9:31:39 PM)
Dr. Puente, how does your research relate to Intelligent Design, if at all?
carlos puente (Mar 25, 2004 9:35:38 PM)
Thanks J. Nelse, well, this research is not classical intelligent design research as practiced by others at ISCID, but certainly the objects that one encounters inside the bell are indeed designs, and the relevance to nature of some of them, i.e., ice crystals and biochemical rosettes, clearly show an intelligent way to think about them. That there is aconnection between the binary expansion of pi and the rosette structure of DNA inside the bell, certainly makes one wonder how is it that such is there.
Originally posted by mattison0922
My point was more akin to if life was based on some fractal equation, then the origin of the equation/formula itself must have had an intelligent source.
Of course, please keep in mind, I know pretty much nothing about fractals other than the basics.
Originally posted by Frosty
They then make the arguement that a designer was needed to... program them initially and therefore does not represent evolution but intelligent design. Wrong.
Evolution does not hinge on the belief of a creator or the non belief of a creator, but whether or not life is capable of evolving.
I have also never heard of a link between Adam's lifespan and the great debate. Maybe they are confused as to what they are saying or are they providing an arguement for both sides?
www.reasons.org...
I am also unsure of the article "Virus Argument No Longer Immune to Challenge". Why does this genetic drift occur?
Originally posted by mattison0922So.... a designer WASN'T required to build and program the initial robots?
Please clarify.
Originally posted by mattison0922Okay... but this thread isn't about evolution, it's about ID. Besides, IDT is an origins theory, and doesn't necessarily stand in opposition to the idea of extant live 'evolving' by any traditional definition.
Originally posted by mattison0922What does Adam's lifespan have to do with IDT?
Originally posted by mattison0922'Reasons' is an Old Earth Creationist site, not an ID site.
Originally posted by mattison0922Your question is vague and not well stated. Genetic Drift occurs as result of alteration of allelic frequencies in reproductively isolated populations as a result of natural selection. What's your issue?
Originally posted by mattison0922What does Adam's lifespan have to do with IDT?
Originally posted by Frosty
I have no idea, I read the article and did not understand it, maybe you should give a it a go.
Originally posted by mattison0922'Reasons' is an Old Earth Creationist site, not an ID site.
Originally posted by Frosty
C'mon, ID is just PC slang for 'creationist'.
Originally posted by mattison0922Your question is vague and not well stated. Genetic Drift occurs as result of alteration of allelic frequencies in reproductively isolated populations as a result of natural selection. What's your issue?
Originally posted by Frosty
No it doesn't, that is what the genetic drift is, but why does it happen they were unable to clarify, so they simply say it debunks evolution?
Instead, modeling studies show that the drug-resistant strains are already present when drug therapy begins. They do not emerge after drug therapy is initiated. In other words, pre-existing strains of RNA viruses happen to be insensitive to specific antiviral drugs, and these continue to live while the drug-sensitive strains die off.
Originally posted by mattison0922
Allelic variation exists. End of story. Allelic variation exists, and allelic frequencies shift as a result of selective pressure. I don't see how it could be anymore clear than this.
The point is that drugs, and selective pressure in general, don't induce genetic change, they exploit pre-existing genetic change. This is true in the case of antibiotic resistance in general. What's so difficult to grasp here?
Originally posted by saint4God
Hey teach, how'd I do?
Originally posted by saint4God
What words do you see here? Imagine these words are exhibited traits. We don't "see" the alleles, rather the "words" that they spell. There will never be an @ to show up. Nor a # or a ? or a %. Why not? Well @, #, ?, or % were never printed on the dice placed inside the cube. DNA is made of up 4 nitrogenous bases - Adenine, Thymine, Guanine, and Cytosine (Urasil in RNA). There will never be 5 bases, nor 3 (does not work either since they need matching pairs). Those are the letters printed on the dice whether we like it or not. It's true that with the length of the DNA strands, that means a LOT of combinations, but can't ame a @ # ? % show up on those dice.
The head of the harpoon is laminated. This means that it is compressible. As it is pushed up the barrel of the gun it will fit tightly and prevent leakage to maintain maximum muzzle velocity. As it emerges from the muzzle it pierces the cuticle of the nematode. At the head emerges it will 'decompress' and make a hole wider than the width of the bore. This will facilitate penetration by the everting tubular "hypodermic".
The gun cell is anchored to the substratum by a mucilaginous glue. It also has a swollen base. When the base is anchored the business end of the gun cell is then tilted upwards at an angle of about 30 degrees which is very suitable for contact with the nematodes and rotifers that graze bacteria in the vicinity of the cell.
The basal vacuole is the power pack for the cell. It is at high Osmotic Pressure. When the gun cell is released the pressure up front is removed and water flows in rapidly through the semipermeable membrane surrounding the vacuole. This squeezes the protoplasm and nucleus, like toothpaste, through the tubular hypodermic. The Haptoglossa gun cell is only about 15 microns long.
Originally posted by mattison0922
My new position as a molecular plant pathologist
An Oomycete (fungus-like organism, but not a true fungus) named Haptoglossa mirabilis infects its host rotifer cells via a miniature cannon called a ‘gun cell’ As the image below suggests, gun cell is an appropriate description based on physical appearance and mechanism.
The basic mechanism of action is described below.
....snip....
Note: The entire process from # 1 - #8 takes place in about 1/10th sec.
Now… the question: Is this an IC system? It’s certainly not homologous to any system I am familiar with, which means pretty much nothing. But there is surprisingly little information about the genetics of such a system.
We could look up sequences, etc, and perform alignments, look for potential homologous genes, etc. In short, we could attempt to support or reject a hypothesis of IC based on circumstantial evidence, ie: gene homologies and other techniques that don’t require us to be in a lab. Most of the resources to perform this type of analysis are freely available on the internet… could be fun and informative. All are welcome to participate, but it’d be nice if we could get some ATS authorities from both sides of the argument in on the fun. Members that come to mind: Rren, Zipdot, Nygdan, Byrd, FatherLukeDuke, etc., though it is understood that mods are especially busy and may not have time to participate in such a project. Feedback?
Originally posted by Rren
Is that anything like a janitor calling himself a sanitation engineer? C'mon Matt fess up. You're just cleaning the beakers and getting coffee for the "real scientists"......
Found another site with pics taken from Chapter 15 of Dr. Barron's "The Nematode-Destroying Fungi" that may be usefull: www.mycolog.com...
Pretty amazing. But when we normally talk about an IRC(ie., designed) molecular machine it's usefull, or serves a positve function in the cell, no? What i mean is that this 'gun cell' seems like a bad thing, so why would you design one...does that make any sense?
Does it perform a neccesarry job or does it only have a negative impact on its host cell?
I'm still reading on this, so these questions may be stupid and/or irrelevant. I get so lost in the jargon when i read ID material sometimes, that it takes me awhile to get a decent grasp of the basics (ie., what's relevant and what's not). I'll reread some of the more technical stuff 10 times before i even comprehend the basics of an issue.....this looks like it's gonna be one of those.
I've been thinking about what IC means quite a bit lately. Normally IDists concern themselves with what components are part of the "IC core"...ie., couldn't have been "built" or evolved via a series of small steps. But, do we not also have to try and identify what system handled this function prior to the component in question being built via an evolutionary process?
What component did the bacterial flagellum's job prior to its "creation" via evolution, or the ATP, cilium, gun cell, etc., etc.?
Forget about the IC argument that the "component parts" are not functional seperate from the "whole" (therefore invisible to natural selection)...but what happens if we remove "the whole"? Is that a seperate question or just a different way to say/ask the same thing?
Originally posted by Rren
Forget about the IC argument that the "component parts" are not functional seperate from the "whole" (therefore invisible to natural selection)...but what happens if we remove "the whole"? Is that a seperate question or just a different way to say/ask the same thing?
Well i'll help wherever i can, but i don't know what help i'd be in "performing alignments, looking for homologous genes, etc". Mostly cause i have no idea what you're talking about. ...[deletia] You said, " techniques that don’t require us to be in a lab" and "resources ... are freely available on the internet" so if us layman can help, tell/show me what i can do and i'm in.
Ok i'm back to the books...where's the best place to start in your opinion? Is there any point in getting Dr. Barron's book? I assume from what i've seen so far that it's intended for scientists and not layman....i'm still trying to understand the captions from the pics in the page i linked.
Originally posted by mattison0922
I have no idea, I read the article and did not understand it, maybe you should give a it a go.
I just read through Virus Argument No Longer Immune to Challenge again, and I don't see anything about Adam. Irrespective of where you got this information, it's irrelevant to ID, as Adam is irrelevant to IDT.
Originally posted by mattison0922
Okay... You're right
Originally posted by mattison0922Your question is vague and not well stated. Genetic Drift occurs as result of alteration of allelic frequencies in reproductively isolated populations as a result of natural selection. What's your issue?
Originally posted by Frosty
No it doesn't, that is what the genetic drift is, but why does it happen they were unable to clarify, so they simply say it debunks evolution?
Not sure what your beef is but did you not read the statement:
Instead, modeling studies show that the drug-resistant strains are already present when drug therapy begins. They do not emerge after drug therapy is initiated. In other words, pre-existing strains of RNA viruses happen to be insensitive to specific antiviral drugs, and these continue to live while the drug-sensitive strains die off.
Allelic variation exists. End of story. Allelic variation exists, and allelic frequencies shift as a result of selective pressure. I don't see how it could be anymore clear than this.
The point is that drugs, and selective pressure in general, don't induce genetic change, they exploit pre-existing genetic change. This is true in the case of antibiotic resistance in general. What's so difficult to grasp here?
Originally posted by Rren
The information below is from an old-earth creationist web-site which I highly recommend(believers and non). These men are real scientists, not the pseudo types that are often seen in the creationist set, and IMO they present a logical and scientific approach to intelligent design that both the believer and non believer can appreciate.Reasons To Believe
Protein Structures Reveal Even More Evidence for Design
By Fazale (Fuz) R. Rana, Ph.D.IN FULL HERE
Recent structural characterization of three proteins, RNA polymerase II, thioredoxin reductase (from E. coli), and chloroplast F1-F0 ATPase, provides exciting additional evidence for Design at the subcellular level.1, 2, 3 These three proteins possess, as part of their architectural make-up, components that are literally machine parts. These new discoveries add to the growing list of molecular motors (enzyme assemblies responsible for cellular movement) and other enzyme systems that are direct analogs to man-made devices
Chains with jaws and hinges:
RNA polymerase II has remarkable machine-like character.9 RNA polymerase II subunits form a channel that houses the chain-like DNA template. “Jaws” help grip the DNA template holding it in place during RNA synthesis. The newly formed RNA chain locks into place a hinge clamp as it exits the RNA polymerase II channel. A funnel-like pore delivers the small subunit molecules to the RNA polymerase II channel. Then the small subunit molecules in the channel are added to the growing end of the RNA chain.
Ball and socket joint:
In a similar vein, structural characterization at 3.0 Å resolution reveals that thioredoxin reductase function is built around a ball and socket joint.10 This enzyme, isolated from the bacterium E. coli, assists in the transfer of electrons between molecules. During the catalytic cycle, the enzyme undergoes a conformational rearrangement that involves the 67° rotation of one of its domains around a clearly defined swivel surface.
Rotary motors:
Finally, recent image analysis by a team from Germany and Switzerland using atomic force microscopy has revealed structural information about chloroplast F1-F0 ATPase. On the basis of this work, we can now add this enzyme to the growing list of ATPase enzymes that are rotary motors.11 As with the other rotary motor ATPases, chloroplast ATPase has a rotor, stator, and turbine.
The watchmaker Arguement, originally from William Paley in 18th century, basically says: as a watch needs a maker, so nature does also.
Skeptics have long argued that nature and a watch are sufficiently dissimilar so that the conclusion drawn from the Watchmaker argument is unsound.
The discovery of enzymes with domains that are direct analogs to man-made devices addresses this concern, because of the striking similarity between the machine parts of these enzymes and man-made devices. Furthermore, as the list of enzymes with machine parts grows, the conclusion of the Watchmaker analogy grows even more certain. Experts in inductive thinking will point out that the more objects taking part in an analogy, the more sound the conclusion arrived at through analogical reasoning.
Seems interesting, that these very small, things have such "designed qualities"......A question: Are these seemingly designed mechanisms believed to have been apart of the original forms of life soon after abiogenesis, and how is this explained in evolutionary theory.
[edit on 25-4-2005 by Rren]