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the moon and the stars that you have ordainged they give you praise.
If the universe wasn't created billions of years ago, then we wouldn't be able to see most distant stars we do.
Source:
http://rationalwiki.com/wiki/Evidence_agai...stant_starlightyou said:
And the firmament shows His handiwork.Only because you WANT to believe it to be so. The human mind believes what it wants to believe.
you said:
The universe, the sun, the moon, the stars, and evWen man himself shows evidence of God's creative capability (man = mankind, people; men and women). See above. It doesn't. Just because you say it does, does not make it so.
you said:
We believe we were created in his image and therefore share many of his attributes.But God is invisible according to the bible. How could we be created in the image of something invisible?
you said:
Why are we the most intelligent creature on the planet?Because we have evolved to be so.
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Why do we alone have to ability to perceive the future, understand the concepts of eternity, etc?
I seriously doubt any human can comprehend eternity.
Squirrels can predict the future. They see winter coming every year, and get ready for it. We are no different.
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Is it because our brains are bigger? No, whales have bigger brains than we do! Elephants and dolphins have large brains as well. We have the capacity for rational thought because we were designed that way.
A. Wow. Do you have any idea how Brains work? Intelligence as we understand it has only somewhat to do with brain size.
http://science-community.sciam.com/blog-en...arter/300006091We EVOLVED THAT WAY. We evolved as some kind of ape/hominid, which are very able at working with tools and building/growing. This, with an additional large brain, allowed our early ancestors to survive more, and become more populous.
Whales on the other hand, are not well equiped like us. They cannot expand their knowledge much in the water, or build, pass down large amounts of knowledge, or develop written language, although they do communicate.
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Consider the many systems of the body and how they work together. From the autonomic to the reproductive, to repiratory and digestive, our sense organs, just to name a few. These are highly advanced systems all by themselves, and yet they work together in us in perfect harmony. This is the complex systems idea I have mentioned before. Others call it irreducable complexity. The first I heard of irreducible complexity was on a thread yesterday but it is similar to my opinion so I will borrow it. The idea is that we are way too complicated to arise by random chance or small changes over long periods of time. Our systems are complex enough to imply the work of a designer.
Our systems slowly developed over hundreds of millions of years. You say a guy snapped his fingers. Which seems more likely to produce something complex?
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Black box: a system whose inner workings are unknown.Scientists use the term “black box” for a system whose inner workings are unknown. To Charles Darwin and his contemporaries, the living cell was a black box because its fundamental mechanisms were completely obscure. We now know that, far from being formed from a kind of simple, uniform protoplasm (as many nineteenth-century scientists believed), every living cell contains many ultrasophisticated molecular machines.
Which works perfectly and provides even more support for evolution. Darwin knew little of the DNA evidence for Evolution, or the evidence hidden within our bodies.
I'd say he's pretty good, aye?(A Christian would claim 'lol PROPHETY!!!')
For DNA and molecular evidence of Evolution inside us, see:
http://en.wikipedia.org/wiki/Evidence_of_c...nd_biochemistryhttp://www.talkorigins.org/faqs/evolution-...h.html#magnoliahttp://txtwriter.com/Backgrounders/Evolution/EVpage13.htmlhttp://www.actionbioscience.org/evolution/ingman.htmlQUOTE
Natural selection can only choose among systems that are already working so irreducibly complex biological systems pose a powerful challenge to Darwinian theory.
What nonsense is this? Slow mutations can easily create another system.(Such as the Eye, or the Brain.)
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We frequently observe such systems in cell organelles, in which the removal of one element would cause the whole system to cease functioning.
You have no idea how organs Evolve, do you? Organs slowly evolve. AT FIRST THEY ARE NOT ESSENTIAL. They grow to be essential over the years.
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The flagella of bacteria are a good example. They are outboard motors that bacterial cells can use for self-propulsion. They have a long, whiplike propeller that is rotated by a molecular motor. The propeller is attached to the motor by a universal joint. The motor is held in place by proteins that act as a stator. Other proteins act as bushing material to allow the driveshaft to penetrate the bacterial membrane. Dozens of different kinds of proteins are necessary for a working flagellum. In the absence of almost any of them, the flagellum does not work or cannot even be built by the cell.
Wow. The Evolution of Flagellum is easily explained.
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):
Step 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.
Step 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).
Step 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).
Step 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.
Step 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.
Step 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).
Linkshttp://www.talkdesign.org/faqs/flagellum.htmlhttp://www.talkreason.org/articles/flag.pdfhttp://www.talkdesign.org/faqs/flagellum_background.htmlhttp://www.talkreason.org/articles/flagback.cfmDunkelberg, Pete. 2003. Irreducible complexity demystified
http://www.talkdesign.org/faqs/icdmyst/ICDmyst.htmlMusgrave, Ian. 2000. Evolution of the bacterial flagella.
http://www.health.adelaide.edu.au/Pharm/Mu...ys/flagella.htmSources: --Matzke, N. J. 2003. Evolution in (brownian) space: a model for the origin of the bacterial flagellum.
---Blocker, Ariel, Kaoru Komoriya, and Shin-Ichi Aizawa. 2003. Type III secretion systems and bacterial flagella: Insights into their function from structural similarities. Proceedings of the National Academy of Science USA 100(6): 3027-3030.
http://www.pnas.org/cgi/content/full/100/6/3027--Cavalier-Smith, T. 1987. The origin of eukaryote and archaebacterial cells. Annals of the New York Academy of Sciences 503: 17-54.
--Cavalier-Smith, T. 2002. The phagotrophic origin of eukaryotes and phylogenetic classification of Protozoa. International Journal of Systematic and Evolutionary Microbiology 52: 297-354.
--Denton, M. 1986. Evolution: A Theory in Crisis. Bethesda, MD: Adler & Adler.
--Hueck, C. J. 1998. Type III protein secretion systems in bacterial pathogens of animals and plants. Microbiology and Molecular Biology Reviews 62: 379-433.
--Kuwajima, G. 1988. Construction of a minimum-size functional flagellin of Escherichia coli. Journal of Bacteriology 170: 3305-3309.
--Matzke, N. J. 2003. (see above)
--Miller, K. 2003. Answering the biochemical argument from design. in: Manson, N. (Ed.), God and design: the teleological argument and modern science, Routledge, London, pp. 292-307.
http://www.millerandlevine.com/km/evol/design1/article.html --Miller, K. 2004. The flagellum unspun. In Debating Design: from Darwin to DNA, 81-97, eds. Dembski, W., and M. Ruse, New York: Cambridge University Press.
http://www.millerandlevine.com/km/evol/design2/article.html--Ussery, D. 1999. (see below)
from:
http://www.talkorigins.org/indexcc/CB/CB200_1.htmlOK. In case you didn't get it, the evolution of flagellum is well backed up by genetic evidence, observation, and reasoning.
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Dozens of different kinds of proteins are necessary for a working flagellum. In the absence of almost any of them, the flagellum does not work or cannot even be built by the cell.
Explained above.
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Constant, regulated traffic flow in cells is an example of a complex, irreducible system.Another example of irreducible complexity is the system that allows proteins to reach the appropriate subcellular compartments. In the eukaryotic cell there are a number of places where specialized tasks, such as digestion of nutrients and excretion of wastes, take place. Proteins are synthesized outside these compartments and can reach their proper destinations only with the help of “signal” chemicals that turn other reactions on and off at the appropriate times
# Despite the complexity of the system that Behe describes, protein transport need not be that complex. Some proteins direct their own secretion so that no transport mechanism is necessary (see references in Ussery 1999). Certainly, other simple systems that could serve as precursors to vesicular transport should be possible.
# Many of the proteins involved in transport in eukaryote cells have molecular "ancestors" in bacteria. These molecules, the ABC transporters, serve in a much simpler system. If Behe is interested in the simplest system that accomplishes a function, why does he not even mention them?
Ussery, David. 1999. A biochemist's response to "The biochemical challenge to evolution". Bios 70: 40-45.
http://www.cbs.dtu.dk/staff/dave/Behe.htmlQUOTE
Still another example is the exquisitely coordinated mechanism that causes blood to clot.
Sigh. Wrong again.
# The blood clotting systems appears to be put together by using whatever long polymeric bridges are handy. There are many examples of complicated systems made from components that have useful but completely different roles in different components. There is also evidence that the genes for blood clotting (indeed, the whole genome) duplicated twice in the course of its evolution (Davidson et al. 2003). The duplication of parts and co-opting of parts with different functions gets around the "challenge" of irreducible complexity evolving gradually.
# Blood clotting is not irreducibly complex. Some animals -- dolphins, for example -- get along fine without the Hagemann factor (Robinson et al. 1969), a component of the human blood clotting system which Behe includes in its "irreducible" complexity (Behe 1996, 84). Doolittle and Feng (1987) predicted that "lower" vertebrates would lack the "contact pathway" of blood clotting. Work on the genomes of the puffer fish and zebrafish have confirmed this (Yong and Doolittle 2003).
Links:Acton, George, 1997. Behe and the blood clotting cascade.
http://www.talkorigins.org/origins/postmonth/feb97.htmlBehe, M. and K. Miller. 2002. Transcript: American Museum of Natural History April 23, 2002 (Part 7).
http://www.ncseweb.org/resources/articles/..._10_31_2002.aspDunkelberg, Pete, 2003. Irreducible complexity demystified.
http://www.talkdesign.org/faqs/icdmyst/ICDmyst.htmlEvoWiki, 2004. Blood clotting.
http://www.evowiki.org/wiki.phtml?title=Blood_clottingMusgrave, Ian, 2005. Clotted rot for rotten clots.
http://www.pandasthumb.org/pt-archives/000884.htmlfrom:
http://www.talkorigins.org/indexcc/CB/CB200_2.htmlQUOTE
Molecular machines are designed.Biochemistry textbooks and journal articles describe the workings of some of the many living molecular machines within our cells, but they offer very little information about how these systems supposedly evolved by natural selection. Many scientists frankly admit their bewilderment about how they may have originated, but refuse to entertain the obvious hypothesis: that perhaps molecular machines appear to look designed because they really are designed.
'If one does not want to find the answer, he will surely not'.
Here's a nice rebuttal to Behe's Work:
http://www.cbs.dtu.dk/staff/dave/Behe.htmlQUOTE
Also, consider the sun. It gives life to everything on this planet. We owe our existence on this planet to this wonder of God's creation. It's amazing how we were placed exactly as far away from the sun that we needed to be in order to live on this planet. With just a few degrees of internal termperature variance, we die. Here's a link to some scientific information about the sun.
So? Some kind of life(perhaps not as we know it) could begin at a variety of temperatures. In fact, this is just as much evidence for God as for Naturalism.
We evolved to live at the distance from the sun we are at simply because that is the only way life could have arisen; all other life wouldn't have made it.
IE- THIS ISN'T EVIDENCE FOR GOD.
Our planet is suitable for life. Hundreds, possibly billions others are. Are we to assume this is a sign of God? Life happened to arise here to live in our temperature range simply because it HAD TO.
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We know that the sun is reducing itself every year as it gives off heat thus expelling life giving energy but at the same time killing itself (entropy). I think it is important to remember that the sun would have been import in allowing evolution to occur billions of years ago. This is not the evolution part, but I'm inserting something interesting about the sun.
'The sun would have been import'?
What does that mean?
Well. that's it.
Also important is that 'irreducable complexity', which you refer to several times, does not hinder Evolution/Abiogenesis, EVEN IF IT DOES EXIST:
http://www.talkorigins.org/indexcc/CB/CB200.htmlOK. Lets sum up the Creation thing, shall we?
A. You start with a lot of baseless claims about how humans are too complex, blah, blah blah.
B. THEN you get into science with Behe's essay.
C. I explain that it is quite simple for organs to evolve.(I'll get into this in my next post)
D. I show you how all of Behe's 'complexity' arguments are not in fact examples of compexity, and could easily have arisen Evolutionarily based on MicroBiological and Genetic evidence.
E. I show you a link which explains why Irreducible complexity isn't a hindrance to Evolution even if it does exist.
Doesn't look like you really got anywhere here. It seems like you tried to give examples that would prove too complex to have evolved, but I showed you they could quite easily.
I'm working on an Evidence of Evolution and Evolution of Organs post
Cheers,
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