B
Let me put this point as strongly as I can. Without these pathways of synonymous texts, these sets of genes that express precisely the same function in ever-shifting sequences of letters, it would not be possible to keep finding new innovations via random mutation. Evolution would not work.
“Let me put this point as strongly as I can. Without these pathways of synonymous texts, these sets of genes that express precisely the same function in ever-shifting sequences of letters, it would not be possible to keep finding new innovations via random mutation. Evolution would not work.”
So, the way he is laying it out is muddy at best. His use of “precisely” is loaded. As stated above, there are ridiculous variations of protein arrangements that perform the same general function. Humans have multiple variations of the same functional proteins ( e.g. haemoglobin). His analogy of randomly changing letters is a bit misleading as well. Many random changes to the text (what I am assuming is the Base or Base Pair) lead to little or no functional changes. Real observable changes occur in the protein chain and one of the four protein form levels, which are dominated by physical and chemical property interactions.The support for common descent given by studies of molecular sequences can be phrased as a deductive argument. This argument is unique within this FAQ, as it is the only instance we can directly conclude that similarity implies relatedness. This conclusion depends upon the similarity of biological structures within a specific context: the similarity observed between ubiquitous genes from different species.
The following discussion is somewhat technical, so it is first presented in the outline of a deductive argument, which makes the logical thread easy to follow. Here are listed the premises of the argument followed by the conclusion and further discussion.
The gist of the argument:
(P1) Ubiquitous genes: There are certain genes that all living organisms have because they perform very basic life functions; these genes are called ubiquitous genes.
(P2) Ubiquitous genes are uncorrelated with species-specific phenotypes: Ubiquitous genes have no relationship with the specific functions of different species. For example, it doesn't matter whether you are a bacterium, a human, a frog, a whale, a hummingbird, a slug, a fungus, or a sea anemone - you have these ubiquitous genes, and they all perform the same basic biological function no matter what you are.
(P3) Molecular sequences of ubiquitous genes are functionally redundant: Any given ubiquitous protein has an extremely large number of different functionally equivalent forms (i.e. protein sequences which can perform the same biochemical function).
(P4) Specific ubiquitous genes are unnecessary in any given species: Obviously, there is no a priori reason why every organism should have the same sequence or even similar sequences. No specific sequence is functionally necessary in any organism - all that is necessary is one of the large number of functionally equivalent forms of a given ubiquitous gene or protein.
(P5) Heredity correlates sequences, even in the absence of functional necessity: There is one, and only one, observed mechanism which causes two different organisms to have ubiquitous proteins with similar sequences (aside from the extreme improbability of pure chance, of course). That mechanism is heredity.
(C) Thus, similar ubiquitous genes indicate genealogical relationship: It follows that organisms which have similar sequences for ubiquitous proteins are genealogically related. Roughly, the more similar the sequences, the closer the genealogical relationship.
“Like protein sequence similarity, the DNA sequence similarity of two ubiquitous genes also implies common ancestry. Of course, comprehensive DNA sequence comparisons of conserved proteins such as cytochrome c also indirectly take into account amino acid sequences, since the DNA sequence specifies the protein sequence. However, with DNA sequences there is an extra level of redundancy. The genetic code itself is informationally redundant; on average there are three different codons (a codon is a triplet of DNA bases) that can specify the exact same amino acid (Voet and Voet 1995, p. 966). Thus, for cytochrome c there are approximately 3104, or over 1046, different DNA sequences (and, hence, 1046 different possible genes) that can specify the exact same protein sequence.
1. Essentially this argument is just a variation on the argument from design. The key difference here is that it misrepresents actual scientific evidence in such a way to support an unscientific conclusion. A more scientific conclusion would be to state that there is some unknown natural phenomenon to explain this apparent "fine tuning". It is also worth mentioning that a counter-argument to design, natural-law argument, and the anthropic principle is also a counter-argument to fine-tuning. See below.
2. A problem arises from the premise that the cosmological constants are in fact 'fine tuned' at all. This premise assumes that there is a certain range of values that each constant could assume. The greater these ranges, the more unlikely that a given set of constants would have assumed the values we observe. However, to simply imagine a certain range of possible numerical values that each constant could assume and calculating the probability that this value would be arrived at by mere chance is fallacious for two reasons. Currently, we have no access to data that would tell us a) what range the constants could possibly assume in reality and b) how many trials there were in which the constants assumed certain values. If in a lottery one number were drawn from a pot of five numbers, then winning the lottery would become comparatively likely. Likewise, even if a trial with an extremely unlikely outcome - say winning an actual national lottery - were repeated a sufficient number of times, the outcome would become likely to occur overall. (See next point)
3. Scientists theorize that given the infinite nature of time and space, an infinite number of other unobservable universes could exist parallel to our own, each with infinite variations of constants. This is known as the multiverse theory. Given infinite possibilities, the formation of a universe such as our own is not so inconceivable.
4. Another flaw with this argument is that it assumes our universe is finely tuned for the sole purpose of supporting life. This is not the case at all. Given the laws of our universe, scientists theorize that our universe is composed of less than 2% baryonic matter, that is matter consisting of protons, neutrons or other particles equal or greater than that of a proton. Dark matter is by far the most common form of matter in our universe. Our universe, if anything, is far more suited for the creation of black holes than it is for supporting life. Life on our planet constitutes only an insignificant portion of our universe.
5. The Earth's total mass is 5.9736×10^24 kg while the estimated total biomass on Earth is around 7×10^13 kg. This means that the percentage of life on Earth is 1.17182269 × 10^-9. That is .00000000117%. The Earth, let alone the universe, is hardly fine tuned for life. Man has created and tested much more finely tuned mediums for simple life in the form of specialized agar solutions that support life/medium ratios far greater than .00000000117%.
6. In order for the probability argument to be valid, the fundamental constants under consideration have to be independent. That is, one cannot claim that the gravitational constant and the speed of expansion of the universe were individually tuned, since they are clearly related. The electromagnetic force is mediated by massless photons which travel at the speed of light, so therefore the strength of this force is likely related to the speed of light. Similar relationships may yet emerge between other constants.
7. If there were a creator who "fine tuned" the universe for our existence, who "fine tuned" the universe in order for said creator to exist? The argument of a creator is infinitely paradoxical.
8. The initial premise of the argument is that in order for life to exist, the universe must have such properties that warrant a designer. However in this line of reasoning, the designer of those properties would exist in a state where none of these properties were true. Therefore any properties deemed to require a designer can't be necessary for existence in the first place, as the designer can exist without them. The argument is self-refuting.
9. If one starts with the assumption that humanity is an accident, the fine tuning argument makes no sense since if we are an accident, no fine tuning was necessary. For the fine tuning argument to make any sense, one has to start with the assumption that humanity is not an accident, which begs the question of a creator. But since the purpose of the argument is to prove that there is a god who created us, any such assumption renders the argument circular.
10. If we are to consider the chance of the universe existing the way it did, surely the same principle of chance can be reversed. What is the chance that a truly omnipotent God, as proposed by many religions, made the constants, factors and general details of the universe as he did? he would have infinite possibilities meaning the probability would be 1 in infinity - much less than the supposed calculations of those presenting the argument.
11. It may be useful to realize that the vast majority of the universe is uninhabitable by any form of life, albeit human life. If there are so many regions of space, and indeed our own planet, that are uninhabitable by life, then why should we call the universe "fine-tuned"?.
12. The argument also seems to call into question the omnipotence of the creator. If he were infinitely powerful, why did he make life constrained to survive only in a tiny fraction of the universe? The case for supernatural intervention would be much more plausible if humans found themselves floating in the vacuum of space, on a toxic planet with no oxygen, or somewhere else where our continued survival was a complete mystery to scientists. As it is, we find life only in areas where the facts of biology tell us it can exist. This is exactly what we would expect if we were not the products of omnipotence.
13. When considering the arguments fourth premise, which includes "...created out of nothing by a single being who is omnipotent, omniscient, all-loving, eternal...", the question must be raised of how does the God being posited as the creator of said universe gain the attributes stated by the argument? the argument is in no way structured to determine the precise attributes of the personal being of which the presenter asserts. It is not necessary for the creator to be all-loving, he could be making us with the notion of torturing us for all we know. It is not necessary for the creator to be eternal, he could have fizzled out in the creation or could have died of some unfathomable cause. And it is likewise unnecessary for the creator to be omniscient and/or omnipotent, there are logical arguments against the proposition of such attributes, and the being need not be all-powerful/knowing - he could just be really, really powerful and know a lot, but not everything.
14. It may be worth noting, also, that the some of the constants specified not not require arbitrary precision. With regards to the Goldilocks zone, the amount Earth can be distanced from the sun is approximately 37%, right out to Mars (yes, our solar system has two planets in the Goldilocks zone). The point being that the so-called precision we find, is actually not that precise in reality (this is one of the more extreme cases, most others can be changed but the difference being not as much).
"Why did God issue just those natural laws and no others? If you say that he did it simply from his own good pleasure, and without any reason, you then find that there is something which is not subject to law, and so your train of natural law is interrupted. If you say, as more orthodox theologians do, that in all the laws which God issues he had a reason for giving those laws rather than others -- the reason, of course, being to create the best universe, although you would never think it to look at it -- if there was a reason for the laws which God gave, then God himself was subject to law, and therefore you do not get any advantage by introducing God as an intermediary." –Bertrand Russell
“According to the anthropic principle proponents, if the universal constants (e.g. gravitation, the strong force, etc.) were just a nose-hair off, the universe as we know it would not exist; stars wouldn't form and there would be no life and no us. That supposedly makes our universe truly special. To demonstrate just how ridiculous this fine-tuning argument is, consider the fact that no measurement in physics is perfect. All of them are approximations and have margins of error. That means the universal constants, that make our universe what it is, have some wiggle room. Within that wiggle room are an infinite quantity of real numbers. Each of those real numbers could represent constants that could make a universe like ours. Since there are an infinite number of potential constants within that wiggle room, there are an infinite number of potential universes, like ours, that could have existed in lieu of ours. Thus, there is really nothing special about our universe.”
― G.M. Jackson, Debunking Darwin's God: A Case Against BioLogos and Theistic Evolution
@Cack,
I can't say I found the 14 arguments all that satisfying or the quote from Bertrand Russell but I'm not sure I really follow the discussion being had.
Did someone argue against evolution? Or that ubiquitous genes cannot be used in the approximation of ancestry? Although I do appreciate the biology refresher, I need someone to help bridge the divide on what's being purported
In regards to your information about how the texts/words metaphor doesn't align itself with the genetic code created by our DNA. You talked about the biological safeguards builtin with codon redundancy but there are many more ways for an amino acid to be affected by a base pair substitution. We can abuse numbers for our purpose here: There are 3 BPs per codon per AA and the redundancy builtin often applies to the 3rd bp so if there is a mutation, you'll still likely get the correct AA. But if you affect either of the previous two codons you are sure to get a different AA. Since there are 3 opportunities to go wrong at each BP and you average three redundancies per AA, you have 6 opportunities to screw it up and 3 opportunities to silently screw it up
This also doesn't take into account catastrophic affects like frameshifts and stop codons being accidentally transcribed.
The nice thing is that we often see minimal effect in protein folding and functionality when a single amino acid is swapped, I'm assuming if swapped, it's better for the swap to occur within the amino acid classes, eg - arginine & histidine
Veritae, my post was in response to Whiskeyjack's prior post with specific questions. My attempt to be concise failed lol. The point of the first part was to expound on how complex but inherently directed evolution is as opposed to randomly occurring. It's so natural that it may be as fundamental to life as a medium is to sound/music. That does not mean it can't happen another way either, it's just the case as we know it to be. Ultimately variation is required but it is not confined to random events and also requires time, heredity etc. happen"
1. The second part was in response to the finely tuned argument. It is ultimately a argument from design, which I find incoherent and unnecessarily anthropomorphized logic. The counter points are simple but I think it exposes several aspects of an argument for design and its assumptions.
2. As to your number crunching... That's not really accurate. Mutation rates are highly variable between species and can speed up or slow down. Environmental changes also can affect Mutation rates Mutation rate - Wikipedia, the free encyclopedia. We are talking x10^-6 and smaller base pairs per group per generation. That is small. Even then, mutations are mostly mute. The real effects are in respect to gene/allele frequencies in populations which is dominated by Natural selection (non-random) pressures.
Just curious wher your assertion about the 15:15:70 idea comes from? Do you have a source I can check to understand better because my understanding of transcription and translation doesn't jive with that. Single point mutations are typically corrected quickly during transcription and during translation there are also several things that prevent errors reading a codon. Errors including 3-6 billion base pairs every time a cell divides result in very few (relatively) errors and certainly not as high or in the manner as I think you are saying.1. It's very difficult to extract out anthropomorphized logic given that everything we sense and experience is through the human lens. I don't really want to make a design argument as I see no purpose for it, inside or outside of a theistic philosophy. I do understand that some of our forum members may believe in some variation of "finely tuned" and I don't see how that has been disproven, since all of these phenomena could come about by a fine tuner.
2. My number crunching still holds. Mutation rates can wax and wane but that variable is simply applied to each codon being transcribed/translated without bias. There may be some published biology papers that can dispel my logic but they'd have to be focused on positional mutation percentages, aka - mutation rate percentages for any given codon have mutation rates across their BPs in a non-uniform pattern, 15%:15%:70%
The rest of what you said I am in agreement with.
It appears this discussion always comes down to a leap of faith in one of two directions:
All things that exist, had a beginning or an inception point. Given that fact, it is reasonable to believe there is a great progenitor that acts as the ultimate end to all of existence.
...or....
The universe/multiverse has always existed, there was no beginning and there will be no true end. Moments of creation are only equaled by moments of destruction and entropy, a sinusoidal pattern that has ruled existence ad infinitum.
Taking Pascal's wager, I tend to fall in the former but I certainly recognize those who put their faith in the other option are not holding an unreasonable position.
Just curious wher your assertion about the 15:15:70 idea comes from? Do you have a source I can check to understand better because my understanding of transcription and translation doesn't jive with that. Single point mutations are typically corrected quickly during transcription and during translation there are also several things that prevent errors reading a codon. Errors including 3-6 billion base pairs every time a cell divides result in very few (relatively) errors and certainly not as high or in the manner as I think you are saying.
I think you misunderstood the intent of my post. I'm not positing there is a high error rate in transcription/translation. I was trying to spell out that the redundancy built in for some codon-AAs only show up on the 3rd base pair. So, let's look at an example to be more specific. My favorite AA, Leucine (tied to skeletal muscle increases) two of it's codons are CUU and CUC, so the third base pair provides the redundancy in case there were a mutation. I was attempting to state, that I would assume mutations across all base pairs in the codon would occur at equal rates. So if the error rate is x 10^-6, then it applies to all BPs in the codon. so there are still better chances that any given mutation will result in either a different amino acid or a stop codon.
Three base pairs per codon, each base pair has the same likelihood of being mutated, which means if a mutation occurs at BP1 or BP2, you definitely get something different than originally intended. If it occurs at BP3, for simplicity sake, we'll say it still gives the same amino acid, since that's where the majority of the redundancy is built in.
With three base pairs per codon, you have twice as high likelihood that any given error in translation will result in a "non-silent" mutation. I can't tell if I'm being too basic or too nebulous in my description. This doesn't take into account the fact that some proteins will still fold correctly or that some amino acids are of the same class and may minimize the effect of any given mutation. It's also possible that a single AA mutation in a protein can reduce it's enzymatic ability drastically, to the point of certainly causing a de novo branch to be selected against in the population.
Obviously, I'm discounting a great deal of complexity seen in this pathway but for our purpose, I believe it still holds true.
What I intended with my previous post was to simply say: if my numbers are wrong, then it'd be due to some academic publishing a paper that describes the relative percentage of BP mutations in any given set of codons. Perhaps it's not true that mutations occur equally across all BPs. To disprove my point above, one would require a study of specific sequences (most likely in yeast or some other fast-propagating organism), which introduced mutagens. You'd then track mutation rate across specific gene sequences to see if there was a biological preference for mutation at a 3rd BP vs 1 or 2. My lab skills have completely atrophied so I'm not sure how you'd setup the study but the underlying theory is explained above.
Let me know if you see an error in this thinking.
This is obviously limited to human non-mitochondrial DNA Mitochondrial DNA does not follow Chargraffs rule. Also other organisms display similar behaviors but with different rates, so its hard for me to agree that "each base pair is equally likely to be mutated"...lolMolecular Human Genetics
The frequency of individual base substitutions is nonrandom
Base substitutions are among the most common mutations and can be grouped into two classes:
Transitions are substitutions of a pyrimidine (C or T) by a pyrimidine, or of a purine (A or G) by a purine.
Transversions are substitutions of a pyrimidine by a purine or of a purine by a pyrimidine.
When one base is substituted by another, there are always two possible choices for transversion, but only one choice for a transition. For example, the base adenine can undergo two possible transversions (to cytosine or to thymine) but only one transition (to guanine; see Figure 9.1). One might, therefore, expect transversions to be twice as frequent as transitions. Because the substitution of alleles in a population takes thousands or even millions of years to complete, nucleotide substitutions cannot be observed directly. Instead, they are always inferred from pairwise comparisons of DNA molecules that share a common origin, such as orthologs in different species. When this is done, the transition rate in mammalian genomes is found to be unexpectedly higher than transversion rates. For example, Collins and Jukes (1994) compared 337 pairs of human and rodent orthologs and found that the transition rate consistently exceeded the transversion rate. The ratio was 1.4 to 1 for substitutions which did not lead to an altered amino acid, and more than 2 to 1 for those that did result in an amino acid change.
Figure 9.1. Transversions are theoretically expected to be twice as frequent as transitions.
Figure 9.1
Transversions are theoretically expected to be twice as frequent as transitions. Blue arrows, transversions; black arrows, transitions.
Transitions may be favored over transversions in coding DNA because they usually result in a more conserved polypeptide sequence (see below). In both coding and noncoding DNA the excess of transitions over transversions is at least partly due to the comparatively high frequency of C [implies] T transitions, resulting from instability of cytosine residues occurring in the CpG dinucleotide. In such dinucleotides the cytosine is often methylated at the 5′ C atom and 5-methylcytosines are susceptible to spontaneous deamination to give thymine (Section 8.4.2). Presumably as a result of this, the CpG dinucleotide is a hotspot for mutation in vertebrate genomes: its mutation rate is about 8.5 times higher than that of the average dinucleotide (see Cooper et al., 1995). Other factors favoring transitions over transversions are likely to include differential repair of mispaired bases by the sequence-dependent proofreading activities of the relevant DNA polymerases.
The location of base substitutions in coding DNA is nonrandom
Nucleotide substitutions occurring in noncoding DNA usually have no net effect on gene expression. Exceptions include some changes in promoter elements or some other DNA sequence that regulates gene expression, and in important intronic sequence positions, such as at splice junctions or the splice branch site (see Figure 1.15). Substitutions occurring in coding DNA sequences which specify polypeptides show a very nonrandom pattern of substitutions because of the need to conserve polypeptide sequence and biological function. In principle, base substitutions can be grouped into three classes, depending on their effect on coding potential (see Box 9.2).
Classes of single base substitution in polypeptide-encoding DNA. On very rare occasions, a single nucleotide substitution within polypeptide-encoding DNA causes defective gene expression by activating a cryptic splice site within an exon (see Figure 9.12). (more...)
The different classes of base substitution listed in the box show differential tendencies to be located at the first, second or third base positions of codons. Because of the design of the genetic code, different degrees of degeneracy characterize different sites. Base positions in codons can be grouped into three classes:
Nondegenerate sites are base positions where all three possible substitutions are nonsynonymous. They include the first base position of all but eight codons, the second base position of all codons and the third base position of two codons, AUG and UGG (Figure 9.2). Taking into account the observed codon frequencies in human genes, they comprise about 65% of the base positions in human codons. The base substitution rate at nondegenerate sites is very low, consistent with a strong conservative selection pressure to avoid amino acid changes (Figure 9.3).
Fourfold degenerate sites are base positions in which all three possible substitutions are synonymous and are found at the third base position of several codons (Figure 9.2). They comprise about 16% of the base positions in human codons. The substitution rate at fourfold sites is very similar to that within introns and pseudogenes, consistent with the assumption that synonymous substitutions are selectively neutral (Figure 9.3).
Twofold degenerate sites are base positions in which one of the three possible substitutions is synonymous. They are often found at the third base positions of codons, but also at the first base position in eight codons (Figure 9.2). They comprise about 19% of the base positions in human codons. As expected, the substitution rate for twofold degenerate sites is intermediate (Figure 9.3): only one out of the three possible substitutions, a transition, maintains the same amino acid. The other two possible substitutions are transversions which, because of the way in which the genetic code has evolved, are often conservative substitutions. For example, at the third base position of the glutamate codon GAA, a transition A [implies] G is silent, while the two transversions (A [implies] C; A [implies] T) result in replacement by a closely similar amino acid, aspartate.
Figure 9.2. Codon frequencies in human genes and locations of nondegenerate, two- and fourfold degenerate sites.
The rate of nucleotide substitution varies in different gene components and gene-associated sequences. On the basis of the above substitution rates and the observation that an average mammalian coding DNA sequence comprises 400 codons, the coding DNA (more...)
I think I get what your saying and it appears to be a form of the Chargroff (sp) rule??? and I have seen that as an assumption for various modeling that base pairs are equally likely to be mutated (changed) but they aren't....
This is obviously limited to human non-mitochondrial DNA Mitochondrial DNA does not follow Chargraffs rule. Also other organisms display similar behaviors but with different rates, so its hard for me to agree that "each base pair is equally likely to be mutated"...lol![]()
Thank God that "Eve" ate that "Apple".
Never really worried about the atheist or the lukewarm Christian. To be honest, not much good in either one of them for the Kingdom of God. I figure both will get their due in the end and wind up at the same place.
What a condescending tone for other people. You wonder why there are atheists that evangelize, its because of people like you that will stricken them to hell for simply not believing in your god. Meanwhile, you don't even care if they are good people, good citizens or care for others.
I doubt they are losing sleep over people like you either.
Not concerned if they are or if they are not. Im nobody to be concerned about. The power that they should be concerned about they clearly arent. If they arent devote followers of Jesus the Bible CLEARLY states the outcome. It doesnt matter if they are good people or good citizens AT ALL. If they are not picking up their cross daily and following Him, whether they are Atheist or lukewarm Christians, the destination is the same.
Maybe you should pick up the Bible sometimes and actually read what it says???
Not concerned if they are or if they are not. Im nobody to be concerned about. The power that they should be concerned about they clearly arent. If they arent devote followers of Jesus the Bible CLEARLY states the outcome. It doesnt matter if they are good people or good citizens AT ALL. If they are not picking up their cross daily and following Him, whether they are Atheist or lukewarm Christians, the destination is the same.
Maybe you should pick up the Bible sometimes and actually read what it says???
IMO, atheism is an extremely arrogant belief-set founded mainly in over-confidence in the "truths" of science. I don't feel like getting into this now as it's a really deep topic and much too complex for a forum post, but there is an awful lot that is inherently flawed about someone saying there is not or must not be a higher power. I understand the choice of agnosticism, I do not understand the choice of atheism.
It's perfectly within someone's rights to believe what Wingman Ray does. It's also perfectly within someone's rights to be an atheist. And there is nothing you can do to prove either viewpoint "right" or "wrong"... such are matters of faith.
IMO, atheism is an extremely arrogant belief-set founded mainly in over-confidence in the "truths" of science. I don't feel like getting into this now as it's a really deep topic and much too complex for a forum post, but there is an awful lot that is inherently flawed about someone saying there is not or must not be a higher power. I understand the choice of agnosticism, I do not understand the choice of atheism.
You seem like a really deep thinker... lol
You sound just like the guy that's always on my college campus. He holds up a sign that says "Take the 'Are You a Good Person?' Quiz!"
You answer a bunch of questions about being a generally good person, and then lastly he asks you if you go to church every Sunday, if you support gay marriage, and if you've accepted Jesus as your lord and savior.
Regardless of how "good" you are after answering his initial questions, if you answer "no" to any of his final three questions, he begins shouting to the entire campus that you will burn in hell for eternity.
Fantastic stuff.
I think you are looking at it wrong, he is obviously a Christian and believes the Bible, which clearly states what he is saying. You may disagree with him but to challenge whether or not he is a "deep thinker" is a pretty arrogant statement just because he firmly believes in his faith
I would be interested in why that is. In my opinion, I don't understand what is fundamentally flawed in thinking that we are not all special creatures.
That maybe... just maybe... the light simply turns off and we become dust in an endless abyss that is the universe. Considering the fact that human life is a grain of sand in the scope of the universe, it see almost "arrogance founded mainly in over-confidence in the belief" of God.
I'm not saying those are my thoughts, but I have never understood why someone believing that we are not a hand-picked population of a higher power, but rather a speck of existence in a much larger plane, is seemed illogical. That almost seems more logical than a magic man in the heavens watching our every move and demanding our allegiance.
Couldn't the vies of Christians who believe in the one true God be considered arrogant, too?
Not concerned if they are or if they are not. Im nobody to be concerned about. The power that they should be concerned about they clearly arent. If they arent devote followers of Jesus the Bible CLEARLY states the outcome. It doesnt matter if they are good people or good citizens AT ALL. If they are not picking up their cross daily and following Him, whether they are Atheist or lukewarm Christians, the destination is the same.
Maybe you should pick up the Bible sometimes and actually read what it says???
That is not what atheism is. Atheism is an affirmative belief set that there are no gods. Atheism does not leave any room for interpretation... as non-compromising Christianity is about there being one God and Jesus Christ, atheism affirmatively states that there are no gods, deities, supreme beings... extrapolated, it's a belief set that fundamentally rejects beings, metaphysical, and other phenomena beyond our comprehension.
I don't get your point here. First of all, the bolded is only a small part of atheism, and isn't the part I find arrogant. Second, I'm not measuring or contrasting the level of arrogance intrinsic to atheism relative to Wingman Ray relative to ISIS relative to...
I'm saying, in a vacuum, there is a ton wrong with core concepts of atheism. There is as much if not more wrong with atheism as any other major religion in terms theological arguments that undermine the integrity of the belief set.
Rejection of the bolded does not necessarily relegate someone to atheism.