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Grengor
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Agreed.Charlie Hatchett said:a. Billions of years are not necessary (but not disallowed either) to create or
produce life.
Where is your calculations for this? This would also assume a constant rate of shrinkage. Measurements from 1980 and above do not show any significant shrinkage. And since they used different techniques back then it was likely to be inaccurate. This is what's known as a PRATT: Point Refuted A Thousand Times. It's claims so rediculous that no self-respecting creationist uses them any longer.Charlie Hatchett said:1. The sun is shrinking at 5 feet/hour which limits the earth-sun relationshipto less than 5 million years. (Significant Acceptance is Assumed for Example
sake)
Again, this is another PRATT. The actual influx of dust on the moon is 240 tons a year, and the original claim was based on a very obsolete measurement, sometimes mistakingly cited as being more recent.Charlie Hatchett said:2. Given the rate at which cosmic dust accumulates, 4.5 billion years would
have produced a layer on the moon much deeper than observed. By
implication, the earth is also young. (Significant Acceptance is Assumed for
Example sake)
Unless you'd like to show me your calculations?
Charlie Hatchett said:b. Irreducible Complexity of Cellular Systems:
1. "An example of an irreducibly complex cellular system is the bacterial flagellum: a rotary propeller, powered by a flow of acid, that bacteria use to swim. The flagellum requires a number of parts before it works -- a rotor, stator and motor. Furthermore, genetic studies have shown that about 40 different kinds of proteins are needed to produce a working flagellum."...Behe and Crew
Untill you get your onw argument in your own words with your own calculations I'm just gonna fight fire with fire.
TalkOrigins said:1. This is an example of argument from incredulity, because irreducible complexity can evolve naturally. Many of the proteins in the bacterial flagellum or eukaryotic cilium are similar to each other or to proteins for other functions. Their origins can easily be explained by a series of gene duplication events followed by modification and/or co-option, proceeding gradually through intermediate systems different from and simpler than the final flagellum.
One plausible path for the evolution of flagella goes through the following basic stages (keep in mind that this is a summary, and that each major co-option event would be followed by long periods of gradual optimization of function):
1. A passive, nonspecific pore evolves into a more specific passive pore by addition of gating protein(s). Passive transport converts to active transport by addition of an ATPase that couples ATP hydrolysis to improved export capability. This complex forms a primitive type-III export system.
2. The type-III export system is converted to a type-III secretion system (T3SS) by addition of outer membrane pore proteins (secretin and secretin chaperone) from the type-II secretion system. These eventually form the P- and L-rings, respectively, of modern flagella. The modern type-III secretory system forms a structure strikingly similar to the rod and ring structure of the flagellum (Hueck 1998; Blocker et al. 2003).
3. The T3SS secretes several proteins, one of which is an adhesin (a protein that sticks the cell to other cells or to a substrate). Polymerization of this adhesin forms a primitive pilus, an extension that gives the cell improved adhesive capability. After the evolution of the T3SS pilus, the pilus diversifies for various more specialized tasks by duplication and subfunctionalization of the pilus proteins (pilins).
4. An ion pump complex with another function in the cell fortuitously becomes associated with the base of the secretion system structure, converting the pilus into a primitive protoflagellum. The initial function of the protoflagellum is improved dispersal. Homologs of the motor proteins MotA and MotB are known to function in diverse prokaryotes independent of the flagellum.
5. The binding of a signal transduction protein to the base of the secretion system regulates the speed of rotation depending on the metabolic health of the cell. This imposes a drift toward favorable regions and away from nutrient-poor regions, such as those found in overcrowded habitats. This is the beginning of chemotactic motility.
6. Numerous improvements follow the origin of the crudely functioning flagellum. Notably, many of the different axial proteins (rod, hook, linkers, filament, caps) originate by duplication and subfunctionalization of pilins or the primitive flagellar axial structure. These proteins end up forming the axial protein family.
The eukaryotic cilium (also called the eukaryotic flagellum or undulipodium) is fundamentally different from the bacterial flagellum. It probably originated as an outgrowth of the mitotic spindle in a primitive eukaryote (both structures make use of sliding microtubules and dyneins). Cavalier-Smith (1987; 2002) has discussed the origin of these systems on several occasions.
2. The bacterial flagellum is not even irreducible. Some bacterial flagella function without the L- and P-rings. In experiments with various bacteria, some components (e.g. FliH, FliD (cap), and the muramidase domain of FlgJ) have been found helpful but not absolutely essential (Matzke 2003). One third of the 497 amino acids of flagellin have been cut out without harming its function (Kuwajima 1988). Furthermore, many bacteria have additional proteins that are required for their own flagella but that are not required in the "standard" well-studied flagellum found in E. coli. Different bacteria have different numbers of flagellar proteins (in Helicobacter pylori, for example, only thirty-three proteins are necessary to produce a working flagellum), so Behe's favorite example of irreducibility seems actually to exhibit quite a bit of variability in terms of numbers of required parts (Ussery 1999).
Eukaryotic cilia are made by more than 200 distinct proteins, but even here irreducibility is illusive. Behe (1996) implied and Denton (1986, 108) claimed explicitly that the common 9+2 tubulin structure of cilia could not be substantially simplified. Yet functional 3+0 cilia, lacking many microtubules as well as some of the dynein linkers, are known to exist (Miller 2003, 2004).
3. Eubacterial flagella, archebacterial flagella, and cilia use entirely different designs for the same function. That is to be expected if they evolved separately, but it makes no sense if they were the work of the same designer.
Do you know what this is? This is an argument from incredulity. It's a logical fallacy and holds no weight in an actual debate. Also, evidence against evolutions is not evidence for design, that's another reason why ID currently isn't science, and untill they toss aside their Creationist yoke they never will be.Charlie Hatchett said:2. Macosko, molecular biology researcher who holds chemistry degrees from Cal and MIT, and Crew at UC Berkeley research lab believe that the work going on inside those bacteria isn't just amazingly complex-it's so incredibly complex that it couldn't conceivably have formed through evolution. The only reasonable explanation, he says, is that these systems and their processes were deliberately created by an "intelligent designer." Macosko, who has co-authored a handful of published scientific papers, calls that designer God, though he says you could call it anything you're comfortable with. If you like, he says, call it space aliens. He is inspired by what he claims is growing evidence that Charles Darwin's theory of evolution-the very bedrock of biology-has collapsed on the molecular level.
No one. Each hypothesis is discussed and tested, and everyone reviews eachother's work. Because the evidence points to a theory, all the scientists gradually accept it, that's exactly what happened when Evolution first reared it's head. If ID is to have any hope to be scientific, they've got a lot of work to do.Charlie Hatchett said:Oh, by the way, who decides or how is it decided if a hypotheses is "proven".
Oh, and from a previous post, the formation of laws and theories are different than they now are. Back in Newton's time, there were natural philosophers that were to find the "underlying laws" in nature that are fixed and never changeable. That was his job. But since science is tentative, meaning it can always be proven wrong, nothing can ever be 100% correct. The problem here is that you're arguing from hundreds of years ago, get with the times man!