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I want to know what are those. So I can ask: why are they not changing?
IF, I were an evolutionist, I WILL devote my whole effort to prove that evolution does happen. Not only we see "change", but it changes to such an extent that we see speciation (however is it defined). So, with that purpose, I will explicitly say in the proposal that I like to see the E. coli evolves into something else (based on some reasons, of course).
The word evolution in that research title is misleading, or confusing, at least.
Is it possible to have a cell made of only dozens biochemicals?
I guess it is not possible today.
If so, does a single cell also evolve? From dozens elements to thousands elements?
Further, do we see the evolution of a single cell today? I am not sure what does this question mean. But it is a question, isn't it?
I don't have any base. I do not know this thing. I am just ask questions.I don't know the specific lower limit, but a simple virus is not much more than a core of DNA/RNA, and a protein capsid (shell). If you're conemplating the first self-replicator, it would be somewhat more than a virus, but less than an amoeba...
If the question were instead; is it possible to have a simple self-replicator which uses fewer than thousands of biochemicals? I think the answer is certainly yes, therefore the picture of early life complexity you're trying to paint fopr abiogenesis here isn't accurate on this point.
You've got a lot of questions, but before we get too far away from it, the original question went unanswered in your reply; upon what basis do you assert that thousands of biochemicals are necessary for life?
I don't have any base. I do not know this thing. I am just ask questions.
So you said "fewer than thousands" in respond to my suggestion of "dozens". I remember ICR people held an argument that even to put one thousand (?) elements together is a practically impossible task. What you say?
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Besides, virus, it is a good idea. How do we define the "species" of virus? Is H5N1 a different species than H1N5? I think virus mutates. Does that fit the idea of speciation?
Without knowing what the first living cell was , how can you assign any quantity to the number of biochemicals necessary for life? Upon what basis do you assert thousands, rather than dozens?
Proteins and enzymes were probably a late addition to life.
Not true. Introduce your reagents onto a crystalline substrate, such as calcite, or a minteral rich in titanium dioxide such as rutile or anatase, and you get an l-enatiomeric excess, which can be further enriched by natural processes. Its also interesting that depositing formamide onto titanium dioxide and exposing it to UV light can give you all of the RNA and DNA nucleotides SOURCE.
True, this is not the case. Life did not arise from a typical homogenous mixture of nucleic acids in a glass erlenmeyer flask. It more likely happened on a mineral substrate, and started off with a small level of enantiomeric enrichment, then was further enriched by day-night cycles of reaction and chemical decomposition. Again, the products of a chemical reaction are predictable, not accidental.
What if the first life form simply was an organelle? Your timeline gets too far ahead of itself too quickly... the first organism you envision is vastly more complex than any that an abiogenesis researcher would suggest as a protobiont (first self-replicator)...
You assume that the first living thing must be as complex as, say, an amoeba. The first life structure might have been as simple as a virus, or mitochondria, so your 'criticism from complexity' don't really withstand scrutiny,
Your argument falls along the lines of a very intelligent re-telling of the fallacious "tornado making an airplane" argument; "what I see is too complex to have formed by accident". To continue that analogy, abiogenesis isn't looking to make an airplane... maybe a hang glider or a paper airplane, at best
Also not true. Abiogenesis has, as of yet, nothing firm for anyone to believe in or investigate, one way or another. Its a very early scientific "work in progress". I'd challenge you to find anyone who 'believes in' it at this early stage. "Believes in what?" shoudl be the normal response. Its like critiquing a film before the first cast member has been chosen, by pretending you know just what the final movie will be like from reading the first draft script alone... I hope once it is a fully developed hypothesis, there will be something more than the usual arguments from incredulity postulated against it.
Have a great day!!
I doubt that very much based on the cell today. What we need to do to determine what it took is to look at what we have now as the bottom line for what constitutes life. There's no reason to think that the first cell was vastly less complex than what we have today.
The cell today is a very complex structure but within it exists very few redundancies or excess parts that are unneccesary for it's function as a living unit.
Most cytologist will tell you that the cell is the basic structure for life.
Anyway here's some basic defintions to consider:
http://en.wikipedia.org/wiki/Life
http://encarta.msn.com/dictionary_1861696586/life.html
The thing we need to do here is to look at the cell and see just how much we could take away and still have life.
To do that all we need to do is go look at the simplest cells i.e. the microbe which doesn't even have a nucleus. Inside a microbe or bacteria there are massive complexities that allow it to survive as a "living" entity in it's environment. I don't see how you could get more basic than the bacteria and still call it life. Certainly virus' are not life neither is prions.
You are describing an intelligently manipulated scenario not a naturally occurring one.
Natural occuring end products outside of living systems will produce both levo and dextro.
In the few and rare places on earth where we find naturally occuring necleotides we always see both produced.
I used the term accidental to describe a non-manipulated by an intelligent designer modality.
There is absolutely no evidence to suggest life started in a fortuitous way.
Statisticaly analysis alone precludes that life as we know it could have resulted from such beginnings.
As a matter of fact just producing a simple protein from randomly occurring molecules would be very hard to do.
Think about what you are saying. Look around and see what exists. If life could have arose from natural pools of organic compounds and a lightning strike we would still see it happeing now.
Sure it does, for life to exist it must be able to do three basic things. It must bring in nutrients , metabolize those nutrients, reproduce, communicate within itself and do all that within a functional cell wall or membrane ( that is a whole different problem in and of itself there ).
The simplest cell complexity wise makes an airplane look like a rock.
For you to have any validity at all you must show using available evidence that a fortuitous origin was possible. No one has done that to date.
Not true my friend. The mainstream paradigm fully accepts abiogenesis as an origin for life.
Here is some articles showing just how much they believe in it.
http://www.talkorigins.org/faqs/abioprob/
You assume that the first living thing must be as complex as, say, an amoeba. The first life structure might have been as simple as a virus, or mitochondria, so your 'criticism from complexity' don't really withstand scrutiny, as it doesn't accurately represent any position within what little investigation is being done in the field of abiogenesis.
Your argument falls along the lines of a very intelligent re-telling of the fallacious "tornado making an airplane" argument; "what I see is too complex to have formed by accident". To continue that analogy, abiogenesis isn't looking to make an airplane... maybe a hang glider or a paper airplane, at best
Reverse engineering and the study of cytology tells us that the bottom line for life is the cell. To survive it has to take in nutrients, metabolize those nutrients, expell waste and reproduce.
Can you show from any valid evidence that life can exist in any less complex form than the cell we have today?
Compared to a very simple bacterium complexity wise an airplane is about like a rock. There are very few redundancies in life. You argue from a faith that something "Could" have existed way back then that was far less complex but have no idea what that could have been.
Reverse engineering and the study of cytology tells us that the bottom line for life is the cell.
To survive it has to take in nutrients, metabolize those nutrients, expell waste and reproduce. There are too many irreducible complex factors in life for it to have taken extremely slow evolving steps to occurr.
Yes, virii.
Again, the goal of abiogenesis is to describe a process that results in a protobiont, a precursor to the first living thing. We see in nature today that there are reproducing things, virii, which show some of the aspects of life (genetic material, descent with modification) and lack some things which most life definitions require (lacks autonomy, doesn't metabolize).
Virii show some interesting properties; as I mentioned above, when a strand of isolated genetic material from the tobbaco mosaic virus is introduced into a solution of its associated protein, its capsid spontaneously reforms, apparently because that is the low energy state for that system.
If virii exist, why cannot other examples of systems with a mixture of living and non-living properties be posited to have existed?
Again with the cytology... Cytology is the study of cells. Of course a study of modern cells is going to consider modern cells the bottom line for modern life. What does this have to do with a process which contemplates the state of things before life existed? Cytology in no way accounts for the conditions of a prebiotic Earth.
Here, you fall victim to utilizing a scientific concept beyond its scope, in much the same way as creationists mistake the theory of evolution for a theory of life origins, you instead are trying to use the principles of cytology as a basis for a critique of the work done in abiogenesis, a field almost entirely separate...
As for reverse engineering, again; abiogenesis, you're doing it backwards.
'Irreducible complexity'; refuted multiple times in multiple ways. Do you have anything recent (from the last two years) on the topic that makes it worth considering again? The bacterial flagellum, the eye, and the mousetrap examples have all been thoroughly refuted...
Primarily because you can't show that one could produce the other based on the bottom line of life today the cell.
The study of cytology in no way makes this discussion conceptually beyond the scope of abiogenesis. As engineers we can figure out how something is made by analyzing it's components and functions.
If you look at something like a car engine it doesn't take too long to figure out what it took to create it piece by piece. The supposed conditions of prebiotic earth are not confirmed by doing trace analysis of the gases in certain rocks.
So they again make assumptions that are not sustained by the evidence. Look here:
http://www.creationresearch.org/crsq/articles/41/41_1/Q%206-04%20Helium%20diffus.htm
How so?
Yes, lets take a look at Mitosis or Meosis. BTW, I disagree that they were refuted especially the flagellum or the eye.
Non sequitur, that is not the goal of the research. Virii merely verify that intermediates between life and non life exist today, and so others might have existed at other times, under other conditions. Remember, you asked for evidence that something simpler than a cell which could be living, but that isn't the goal of abiogenesis, where most intermediates (other than possible the protobiont) would certainly be non-living things.
Analyzing life as a collection of engineered components is your intellectual pitfall. Like the cytologist-cell example you offer, you cannot conceive of anything simpler than the systems with which you are personally familiar... Its no wonder that the modernized 'Paley's watchmaker' argument is so appealing to you.
Gentry picked as poor a location for helium analysis as he could possibly find.
Is there anything more recent? I've read the 2004 paper...
Have their helium analyses of 2004 been re-confirmed in any location absent the ridiculously complex thermal history of the Fenton Hill site?
Has another research group confirmed the three valid samples (out of six) with high helium content?
Humphries says his rock samples were hot granite, but site surveys record gneiss at the depths that he sampled (750 and 1490 meters)... has the identity of the source rock been resolved/confirmed?
Has he revised to include all relevant measurement errors and variabilities?
Even if Humphries is right, and a billion years of radioactive decay happened in a week, where did all of the heat from that event go to, and why is there an Earth around after such an event?
Underground helium deposits are mined in New Mexico because of their abundance. Has anyone confirmed whether or not the surrounding area is yet another helium-rich location, which would more or less confound any quantiative helium analysis in the area?
Ask an exploration geologist (preferably, a Christian one) what he thinks of helium analysis of that site...
Abiogenesis is the investigation of possible processes which progress from non-living chemicals to living systems, through a series of stages. If you are going to attempt to argue against abiogenesis, it makes little sense to start with the last step (a living cell), leap from there all the way back to simple chemicals, and just state that you cannot conceive of how it happened. If you are going to argue against abiogenesis, argue against abiogenesis... follow the process (basic chemicals -> polymers -> self replicating polymers -> hypercycle -> protobiont -> living cell) and not your guess as to what it might look like, when run in reverse.
Each time Behe and Denton claim that this or that flagellum is irreducibly complex, somethign comes along to refute them. Denton's blunder with the 9+2 tubulin cilia comes to mind. Take a bacterial flagellum, and remove the P and L rings, and its still a functioning bacterial flagellum. Is there anything you've got on the topic which is something new, say from 2007 or 2008? As far as I know ,they haven't come up with anything new (since the last update to Matzke's essay; http://www.talkdesign.org/faqs/flagellum.html) Otherwise, the ball remains in Behe and Denton's court to pony up the next example to refute... I think that I've seen enough instances of the failure of irreducible complexity in its first decade as a concept, to be comfortable rejecting the idea as having merit.
http://www.ncbi.nlm.nih.gov/pubmed/10704296?dopt=Abstract
Thornhill is a good reference for understanding why IC systems are not actually irreducible, and can be evolved from simpler precursors in almost any circumstance...
[edit - I see you have a thread dedicated to IC. If it makes things easier for you, cut and paste the IC segment above there, and we can keep a discussion going on that topic in a more appropriate thread... No sense in you duplicating your efforts on a topic in two threads.]
What I asked for and what you gave are not congruous or provide the challenge of showing intermediacy for life.
Virus are not alive, nor will they ever be.
I don't remember saying anything about "Paley's" watchmaker's argument. Where did that come from?
Analyzing living systems as a collection of engineering components is not necessarily a down fall for me but shows teleological appropriatness because there is an obvious "design" in place for such complexity to function.
There's other studies that show the same thing in other places.
I don't buy into that amount of decay in a week. Nor do I buy into the speed of light exponentially being faster either. Things would get to screwy physics wise for that.
I already have and he agrees with the author of the article.
I can do that statistically and show the near impossible chance of amino acids or proteins forming from random modalities but you would dismiss that as well.
No, my friend, I can look at the end product and tell it didn't just happen by fortuitous random means. Even a small child could see that.
Is the appearance of design the same as actual design? No. What's more, if you're arguing from the perspective of Christian creation, it would seem you are arguing for a god who only creates by improbable routes, and not the probable ones. Here's an example of what I mean (taken from a creationist, no less)
Say an avalance occurs, making a large pile of rubble. Sometime afterwards, rain washes away all of the little stones and the mud and dirt, leaving behind a framework of large stones perched one atop the other in an intricate, interdependent framework. Pull away any one large stone, and the structure would collapse. It looks as if each rock were deliberately placed such that all the gaps and crevices were deliberate, and it is a complex, balanced, interdependent system, but no design was originally conceived. Its an elegant analogy to the current living system framework;
In other words, if the hypercycle which generated the protobiont was itself efficient enough to outcompete all previous polymer catalytic processes in competition for resources, the hypercycle would collapse shortly after generating the protobiont, and leave no evidence of its passing (any raw materials that it was using would be taken up by the protobiont, which uses them for replication). You, looking at current life systems with another few billion years of evolution thrown into the mix, cannot envision the original hypercycle because of the complexity of the structures life currently has...
Got sources?
Then please tell me why there isn't a radioactive hole in the ground where Fenton Hill, NM is found. If all of that helium was made by radioactive decay in a few thousand year time frame as the authors assert, it generated heat while it occurred, enough to melt the surrounding landscape. And yet, no one in Los Alamos seems to have noticed...
It's always funny to me to debate this. Giving examples of randomly piled rocks eroded away to compare with what may have happened for unassisted abiogenesis to be valid is like comparing the crystalline structure of the silica in a computer chip to the computer itself.
Talk about ludicrous!!!! ID is very detectable to anyone with a modicum of intelligence themselves.
All you have to do is look at the complexity of the systems or the biochemistry in the cell to see it could never have just happened by fortuitous means.
Look at this little article and explain how a chaperone or chaperonin molecule could just happen.
http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/D/DenaturingProtein.html
This is nothing more than pure speculation. If your premise is valid then we should still be able to find hypercycles in the sub-oceanic hot vents where they say life began.
IOW, we should still see life emerging from these speculative mechanisms.
Here's an article on this that shows it's not just that particlur place in New Mexico that shows Helium retention.
http://www.minsocam.org/ammin/AM26/AM26_403.pdf
The main issue to me in radiometric dating is that so many assumptions have to be made to be able to come up with the proper ratios.
In situ analysis is always made being subject to enviromental influences like water or near by radioactive sources that may be different.
atomweaver,
Do you believe life started from unassisted abiogenesis,
or are you just positioned on the opposite side of me for the debating sake of it all?
I don't buy into that amount of decay in a week. Nor do I buy into the speed of light exponentially being faster either. Things would get to screwy physics wise for that.
EXAMINING THE DATA
The data obtained over the last 320 years at least imply a decay in 'c' [56]. Over this period, all 163 measurements of light-speed by 16 methods reveal a non-linear decay trend. Evidence for this decay trend exists within each measurement technique as well as overall. Furthermore, an initial analysis of the behaviour of a number of other atomic constants was made in 1981 to see how they related to 'c' decay. On the basis of the measured value of these 'constants', it became apparent that energy was being conserved throughout the process of 'c' variation. In all, confirmatory trends appear in 475 measurements of 11 other atomic quantities by 25 methods. Analysis of the most accurate atomic data reveals that the trend has a consistent magnitude in all the other atomic quantities that vary synchronously with light-speed [56].
All these measurements have been made during a period when there have been no quantum increases in the energy of atomic orbits. These observations reinforce the conclusion that, between any proposed quantum jumps, energy is conserved in all relevant atomic processes, as no extra energy is accessible to the atom from the ZPF. Because energy is conserved, the c-associated atomic constants vary synchronously with c, and the existing order in the cosmos is not disrupted or intruded upon. Historically, it was this very behaviour of the various constants, indicating that energy was being conserved, which was a key factor in the development of the 1987 Norman-Setterfield report, The Atomic Constants, Light And Time [56].
The mass of data supporting these conclusions comprises some 638 values measured by 43 methods. Montgomery and Dolphin did a further extensive statistical analysis on the data in 1993 and concluded that the results supported the 'c' decay proposition if energy was conserved [60]. The analysis was developed further and formally presented in August 1994 by Montgomery [61]. These papers answered questions related to the statistics involved and have not yet been refuted.
ATOMIC QUANTITIES AND ENERGY CONSERVATION
Planck's constant and mass are two of the quantities which vary synchronously with 'c'. Over the period when 'c' has been measured as declining, Planck's constant 'h' has been measured as increasing as documented in the 1987 Report. The most stringent data from astronomy reveal 'hc' must be a true constant [62 - 65]. Consequently, 'h' must be proportional to '1/c' exactly. This is explicable in terms of the SED approach since, as mentioned above, 'h' is essentially a measure of the strength of the zero-point fields (ZPF). If the ZPE is increasing, so, in direct proportion, must 'h'. As noted above, an increasing ZPE also means 'c' must drop. In other words, as the energy density of the ZPF increases, 'c' decreases in such a way that 'hc' is invariant. A similar analysis could be made for other time-varying 'constants' that change synchronously with 'c'.
This analysis reveals some important consequences resulting from Einstein's famous equation [E = mc[SIZE=-1]2[/SIZE]], where 'E' is energy, and 'm' is mass. Data listed in the Norman/Setterfield Report confirm the analysis that 'm' is proportional to 1/c[SIZE=-1]2[/SIZE] within a quantum interval, so that energy (E) is unaffected as 'c' varies. Haisch, Rueda and Puthoff independently verify that when the energy density of the ZPF decreases, mass also decreases. They confirm that 'E' in Einstein's equation remains unaffected by these synchronous changes involving 'c' [16].
If we continue this analysis, the behaviour of mass 'm' is found to be very closely related to the behaviour of the Gravitational constant 'G' and gravitational phenomena. In fact 'G' can be shown to vary in such a way that 'Gm' remains invariant at all times. This relationship between 'G' and 'm' is similar to the relationship between Planck's constant and the speed of light that leaves the quantity 'hc' unchanged. The quantity 'Gm' always occurs as a united entity in the relevant gravitational or orbital equations [66]. Therefore, gravitational and orbital phenomena will be unchanged by varying light speed as will planetary periods and distances [67]. In other words, acceleration due to gravity, weight, and planetary orbital years, remain independent of any variation of 'c'. As a result, astronomical orbital periods of the earth, moon, and planets form an independent time-piece, a dynamical clock, with which it is possible to compare atomic processes.
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