Posts Tagged ‘origins’

The following is a re-posted article from:

Origins Science Needs Design Rehab

The following article was written by Dr John C Walton in response to an article by Richard Dawkins and Jerry Coyne which was published in the Guardian on 1 September 2005. Dr Walton’s response was sent to the Guardian on Tuesday 20 December 2005 but not published. Dr. Walton is Professor of Reactive Chemistry at St Andrews University.

Are highly accredited scientists like Professor John Walton “ignorant, stupid, insane (or wicked)” because they reject the ‘molecules to man’ view of origins? This is what Richard Dawkins would apply to scientists like him. With prestigious qualifications Professor Walton surely has a right to object! He can be found speaking on the Edinburgh Creation Group.

During the last decade a fresh, enlightening breeze has been blowing into every corner of the house that Darwin built. The enterprise promoting this sea change, known as Intelligent Design (ID), started to cohere in the mid 1990s. Lehigh University biochemist Michael Behe published his book Darwin’s Black Box in which he convincingly showed that many biological structures display “irreducible complexity”. Structures like vision cascades, cellular cilia, bacterial flagella and other “molecular machines” require many complex and coordinated molecular working parts. Behe combed the literature in search of evolutionary scenarios involving many small steps, to account for the origin of such structures, but found them few and far between and totally inadequate. For biological machines to work, all (or most) of the molecular parts are needed at once, i.e. the complexity cannot be reduced to some much simpler state. Individual component proteins, or small selections of them, do not function at all and hence the Darwinian mechanism cannot build the observed complexity by gradual selection of increasingly efficient precursors. Irreducibly complex mechanical and electronic machines offer a pertinent analogy and are known to be the products of intelligent minds taking advantage of natural laws. Consequently, Behe argued that biological machines are powerful evidence of intelligent design in biology.

At about the same time Berkeley Law Professor, Phillip Johnson, applied his relentless logic to show that the full diversity of Darwinian evolution is not supported by compelling factual evidence from palaeontology or by empirical data from biology (see his book Darwin on Trial). Most importantly, Johnson highlighted the fact that the main support for Darwinian Theory derives from its philosophical assumptions. Evolutionists see science as essentially materialist and based on philosophical naturalism. Only chance and the laws of nature are admitted as acceptable explanatory tools. Any interpretation departing from this narrow arena will automatically be rejected as non-science or worse still as superstition.

But how is it possible to decide if something has been designed or if the design is only apparent? An important step was taken by mathematician and philosopher William Dembski who established criteria for detecting design. Dembski drew attention to the fact that detecting design is already a well established scientific activity in fields such as forensic science, archaeology and cryptology. Methods employed with obvious success in these areas to distinguish criminal from accidental activity, to differentiate artefacts from natural objects and to decode messages, should also be applicable to biological structures and to events in nature. In his book The Design Inference Dembski described a general method he called “specified complexity” for identifying design and distinguishing it from the effects of natural causes. He demonstrated that systems exhibiting high complexity combined with “specification” are always produced by intelligent agents. To be “specified” an object or event must correspond to an independent pattern or dynamic sequence. An example of specification would be a dart board with a bulls eye in the centre. The bulls eye is the specified target. Randomly throwing darts is unlikely to result in hitting a bulls eye. There is something special about hitting a bulls eye in a board on a wall that is very different from throwing darts then drawing a bulls eye around them wherever they hit. The difference is that the bulls eye is specified. It turns out that nature, and particularly biology, is equivalent to a long series of bulls eyes that have all been hit by darts. When something has the property of specified complexity it is logical and rational to conclude it was designed.

Dembski, Stephen Meyer and others have applied the specified complexity criterion to biological phenomena and find good agreement with Behe’s conclusion that their origin implies intelligent design. It is especially significant that the Intelligent Design criterion enables data from across a spectrum of scientific areas to be rationalised. Physicists have discovered that the existence of life in the universe depends on a highly improbable balance of fundamental factors, often referred to as the “fine tuning of the universe” or as “anthropic coincidences”. Application of the specified design criterion to this cosmic enigma also signals intelligent design as the most likely cause.

It is apparent that this is a fresh, logical and rational way of thinking, which enables design to be detected independently of any philosophical or religious beliefs. Objective thinkers will welcome this as a way of shedding light on some of science’s most perplexing impasses. In practise Intelligent Design is growing in influence among scientists and philosophers who are willing to consider design as a third fundamental cause along with chance and natural law. On the other hand the old school of materialists, who hold that only chance and necessity are admissible causes, oppose Intelligent Design with every means their powerful establishment positions give them.

Richard Dawkins and Jerry Coyne are long-time members of this vintage group and are adamantly opposed to Intelligent Design. No surprises there! Distinguished philosopher of science Karl Popper wrote “the wrong view of science betrays itself in the craving to be right”. The intolerant tone of the article written by Dawkins and Coyne “One Side Can Be Wrong”, which appeared in the Guardian Newspaper on September 1st. 2005 is a pity, and shows an emotional and ideological attachment to their world-view has led them deeply into wrong territory. For them evolution should brook no rivals. Origins research is one of the softest sciences so proponents particularly need to avoid the craving Popper spoke of and to cultivate an impartial and objective attitude. It is worth taking time to evaluate the more coherent of the points made in the article.

One label Dawkins and Coyne immediately stick on Intelligent Design is: “There is nothing new about Intelligent Design. It is simply creationism camouflaged with a new name.” The major players in Intelligent Design science emphatically reject this assertion. Proponents of Intelligent Design regard it as a scientific research programme that investigates the effects of intelligent causes. Intelligent Design advocates such as Michael Behe and William Dembski are not young earth creationists and do not reject evolution. For Dembski the purpose of Intelligent Design is “to rehabilitate design as a mode of scientific explanation.” Meyer wrote “The question that must be asked about the origin of life is not ‘which materialistic scenario seems most adequate?’, but ‘what actually caused life to arise on the earth?’”. The specified complexity criterion for detecting design makes no appeal to sacred books and is independent of all religious authority. Phillip Johnson remarked that, “Our objective is not to impose a solution, but to open the most important areas of intellectual inquiry to fresh thinking”. Of course Intelligent Design research has important implications for creationism, but support for creationism is not its objective. Intelligent Design advocates accept evolution, but they doubt that it can do everything that Darwinists claim. Their purpose is to ‘follow the evidence wherever it leads’. This statement has become a slogan of Intelligent Design advocates, and is entirely in harmony with the open-minded attitude with which any scientific investigation should be pursued. It is important to understand that Intelligent Design is not a claim that miracles occur. Rather, it seeks to establish if design is an actual feature of the universe that cannot be duplicated by the effects of natural law and chance.

Early in their article Dawkins and Coyne say “So, why are we so sure that intelligent design is not a real scientific theory, worthy of “both sides” treatment? Isn’t that just our personal opinion? It is an opinion shared by the vast majority of professional biologists . .”. “If Intelligent Design really were a scientific theory, positive evidence for it, gathered through research, would fill peer-reviewed scientific journals. This doesn’t happen. It isn’t that editors refuse to publish Intelligent Design research.” As already mentioned, for material naturalists “real science” only admits chance and necessity as valid causes. Dawkins and the majority of his evolutionary peers automatically rule out Intelligent Design on these philosophical grounds and consider it a waste of time to evaluate the evidence. The majority of professional biologists work in institutions dedicated to evolution and its sister disciplines. Many institutes are specifically named “Evolutionary Biology” or some variant of this. The research funding, the livelihoods, the careers, the professional reputations of all these scientists depend on adherence to evolutionary orthodoxy. Objectivity on foundational questions of origins is not an option for them in these circumstances. The majority scientific opinion cannot be taken as a trustworthy yardstick for gauging the validity of Intelligent Design. In any case, Dawkins and Coyne, after making their misleading point admit that it is nonsense: “[But of course science does not proceed by majority vote among scientists.]”

It is totally unsurprising that Intelligent Design research is not reported in mainline science journals. Contrary to Dawkins and Coynes’ assertion, editors routinely refuse to publish. When Dr Richard Sternberg, editor of the Proceedings of the Biological Society of Washington, published a single paper by Cambridge educated Stephen Meyer making the case for Intelligent Design, he immediately became the subject of a closet campaign of ridicule and intimidation. “They were saying I accepted money under the table, that I was a crypto-priest, that I was a sleeper cell operative for the creationists” said Sternberg. He was advised not to attend a biological society meeting because feelings were running so high order couldn’t be guaranteed. An independent agency, the US Office of Special Counsel, examined email traffic emanating from the Smithsonian Institution, where Sternberg held a fellowship, and noted that “retaliation came in many forms … Misinformation was disseminated through the Smithsonian and to outside sources. The allegations against you were later determined to be false” (see: for Sternberg’s own restrained account of the affair). Editors are well aware of the intimidation and harassment they will face so it is small wonder they shy away from publishing articles favourable to Intelligent Design. It is ironic for Dawkins of all people to denigrate Intelligent Design because, “Its advocates bypass normal scientific due process by appealing directly to the non-scientific public and – with great shrewdness – to the government officials they elect” when these are exactly the methods he adopts himself! His main contribution to science is the series of popular books expounding his brand of evolution to the general public. In fact Dawkins is following a long line of evolutionists including Charles Darwin, Thomas Huxley and Stephen Gould all of whom have appealed directly to the non-scientific public in books and popular articles. Dawkins and Coynes’ belief that it is fine for evolutionists to appeal directly to the public, but wrong for those who disagree with them, is deeply revealing of their ultra-partisan approach.

According to Dawkins and Coyne, Intelligent Design scientists make unreasonable demands for evidence: “One side (Evolution) is required to produce evidence, every step of the way. The other side is never required to produce one iota of evidence, but is deemed to have won automatically, the moment the first side encounters a difficulty – the sort of difficulty that all sciences encounter every day, and go to work to solve, with relish.” For over a century evolutionary scientists have been promising that laboratory science will someday discover a quantifiable mechanism for evolutionary change. Scientifically rigorous explanations have also been promised for: how life originated; how the genetic code and new genetic information could arise; how complex biological organs like eyes, cilia, etc. originated; how new biological species developed from ancestral forms and why the fossil record does not show the “innumerable transitional forms” Darwin expected. Intelligent Design scientists do not denigrate the huge progress that biologists have made in understanding how smaller changes have come about, how new varieties of animals and plants are produced, i.e. microevolution in general. Evolutionists assert that the large steps to really new structures (macroevolution) are just an accumulation of smaller steps. It is very significant however, that even after all this time, verifiable laboratory evidence is completely absent, the fossil record presents major problems, and only fanciful “scenarios” are on offer. The point Intelligent Design scientists are making is that the time has now come to examine alternative explanations in which design is evaluated alongside natural causes. The relish with which scientists work in solving origins problems could be pleasantly enhanced by adding the Intelligent Design criterion to their arsenal of scientific tools.

Dawkins and Coyne believe: “Biologists, on the other hand, can confidently claim the equivalent “cinematic” sequence of fossils for a very large number of evolutionary transitions. Not all, but very many, including our own descent from the bipedal ape Australopithecus.” This claim is seriously at odds with considered opinion in the scientific literature emanating from specialists in palaeontology. For example, Kemp says “the observed fossil pattern is invariably not compatible with a gradualistic evolutionary process” (Fossils and Evolution, Oxford University Press, 1999, p. 16; see also: Carroll, Patterns and Processes of Vertebrate Evolution, Cambridge University Press, 1997, p. 8-10.) Even evolutionist icon Stephen Gould admitted: “The history of most fossil species includes two features particularly inconsistent with gradualism: 1. Stasis. Most species exhibit no directional change during their tenure on earth. They appear in the fossil record looking pretty much the same as when they disappear, morphological change is usually limited and directionless; 2. Sudden appearance. In any local area, a species does not arise gradually by the steady transformation of its ancestors; it appears all at once and fully formed.” The fossil record does not supply evidence for macroevolution. What is more, if the fossil record were really as portrayed by Dawkins and Coyne, there would have been no need for the “Punctuated Equilibria” hypothesis to have been formulated to try and explain the universal gaps.

Dawkins and Coyne keep up their courage by suggesting: “And – far more telling – not a single authentic fossil has ever been found in the “wrong” place in the evolutionary sequence. Such an anachronistic fossil, if one were ever unearthed, would blow evolution out of the water. As the great biologist J B S Haldane growled, when asked what might disprove evolution: “Fossil rabbits in the pre-Cambrian.”” This is to seriously underestimate the capacity of evolution to absorb bad news! When it comes to the fossil record, even Charles Darwin admitted that it was strong evidence against his theory and appealed to the incomplete nature of the record to try to get around this. Not surprisingly, Dawkins and Coyne also appeal to the incompleteness of the record. But appealing to fossils that have not been found, and trying to explain away those that have been found, hardly constitute strong evidence supporting Darwinism. There is a great deal of flexibility about exactly what the right evolutionary sequence is. Furthermore, geochronology is far from an exact science. Different dating methods frequently give discordant results. Samples for radioactive dating may contain contamination from younger material or from older source rock so that the classify them either as intrusive, i.e. buried at a later date by human or natural means, or they are labelled frauds. Enough doubt can always be thrown. For a recent example, consider the report by Bennett, Huddart et al. of fossil human footprints in volcanic ash near Puebla, Mexico, dated to 40,000 yr by a variety of techniques including radiocarbon analysis (“right” date can usually be found, either by “selection” from available samples or by selection from the range of dates. A nice example of this process unconsciously in action during the controversy over the date of skull KNM ER 1470 from the Lake Turkana region of Kenya is described by Roger Lewin in his book “Bones of Contention”. Nor do grossly out of place fossils like rabbits in the pre-Cambrian present any threat to evolution. Evolutionary palaeontologists “know” such fossils are impossible and therefore they always classify them either as intrusive, i.e. buried at a later date by human or natural means, or they are labelled frauds. Enough doubt can always be thrown. For a recent example, consider the report by Bennett, Huddart et al. of fossil human footprints in volcanic ash near Puebla, Mexico, dated to 40,000 yr by a variety of techniques including radiocarbon analysis which challenged evolutionary views about the timing of human entry into the Americas. No surprise that it was rapidly followed by a rebuttal from Renne et al. (Nature 2005, 438, E7) re-dating the footprints by a gigantic leap to 1.3 Myr and redefining them as “markings” caused by erosion. Although many anachronistic fossils have been found, evolution routinely shrugs them off.

Dawkins and Coyne assure us that: “In fact, the bacterial flagellum is certainly not too complex to have evolved, nor is any other living structure that has ever been carefully studied. Biologists have located plausible series of intermediates, using ingredients to be found elsewhere in living systems”; but this is largely wishful thinking. What is meant by “located”? Does this mean located in the fossil record, located in laboratories or located in the imagination? When it comes to explaining the origin of the bacterial flagellum, and similarly complex, information-rich biological organelles, evolutionary ingenuity has found little to offer, as recourse to biochemistry textbooks and journals has demonstrated. Of course, a few, short “plausible series of intermediates” for these organelles may be “located” in imaginary scenarios regarded even by their originators as incomplete and highly tentative. Scientific imagination knows no limits! But the broad picture of this area of evolution is noteworthy for the scarcity of ideas and their insubstantial character.

The oft repeated dictum “evolution is fact” has become a password ritually affirmed by orthodox Darwinians. Even distinguished academics like Dawkins and Coyne clutch this shaky prop. “The weight of the evidence has become so heavy that opposition to the fact of evolution is laughable to all who are acquainted with even a fraction of the published data. Evolution is a fact: as much a fact as plate tectonics or the heliocentric solar system.” The trouble is, the word evolution has become too ambiguous in its meaning. In many contexts “evolution” means simply change, and who would deny change in the natural world? There is indeed a large volume of evidence that microevolution happens. This is not in dispute; but neither is this the process Intelligent Design scientists are addressing. To quote Phillip Johnson “The point … is whether it (microevolution) tells us anything important about the processes responsible for creating birds, insects and trees in the first place.” All the evidence favouring evolution is of the “finch beak” kind; small variations within a known species or closely related group of species. Fossil sequences of trilobites showing size gradations are well known, as are the laboratory experiments developing fruit flies with divergent morphology. The problem is that this kind of evidence does little to advance knowledge of how trilobites or fruit flies came into existence in the first place. That evolution was supposed to be about the origin of species has become lost in a maze of trivia.

For about 150 years science has striven mightily to explain the origins of everything in terms of only chance, allied with the laws of nature. Dawkins and Coyne offer nothing new, just the same unsubstantiated assertions and unfulfilled promises that have led origins science into decades of sterile wandering. Origins science seems gripped in a mesmeric addiction to games of chance. It is now time to check into design rehab. Their article shows that Dawkins and Coyne are still in full denial. The prime objective of the Intelligent Design enterprise is to establish design as a basic cause, along with chance and natural law, and hence to advance understanding of how complex biological and other structures originated. There are hopeful signs that a new generation is recognising this as a logically sound, rational and reasonable programme.

John C Walton (St Andrews, December 2005)



What happens when you put a frog in a blender and turn it on? The Frog dies, his body becoming a mish-mash of liquefied flesh, tissue and blood. Kind of gross to think about, right? Now if I take this puréed of frog juice and heat it up, or freeze it, or send 100 volts of electricity through it, will the frog-juice ever reassemble itself back to the frog it once was? Nope. In fact, no matter what you do to the frog-juice, it never reassembles itself back into a frog. But why not?

The following article is based off of questions I’ve had from my Biology 140 class on Human Genetics, and my Biology 100 Lab course. This article contains no theories or conclusions, just facts followed with questions. I’m curious as to what your conclusions are after reading these facts, and what your answers are to my questions.

But back to the frog in the blender; it’s still sitting there in the blender container a mish-mash of frog juice. No frog has yet to emerge… A similar experiment is done by biologists, but not with frogs. A small eukaryotic cell is placed in sterile test tube. The test tube is filled with distilled water, at the perfect temperature and alkalinity for the cell’s environment. The cell’s membrane is then punctured with a needle. With the membrane wall punctured all of the internal components of the cell (organelles) begin to spill out into the test tube water. What happens next? The test tube has within it all the necessary components of a living cell, yet the cell dies. The floating organelles themselves never arrange themselves into another living cell even though all they need to do so is right there in the test tube. Why is this? Why don’t the organelles organize themselves into another living cell?

Let’s look at something smaller though. Let’s look at the basic building block of life; DNA. DNA is the absolute prerequisite for life. The world’s first living thing ever to exist on earth had DNA. In order for a living organism to live (grow and reproduce) its DNA must perform three functions; replication, transcription and translation.[1]


In order for an organism to grow its DNA must replicate itself to make more DNA. The DNA unwinds, breaks, builds a new nucleotide chain, and then mends, producing two DNA strands where there was just one before. The DNA is unwound by an enzyme called a helicase which then holds the strand open while another enzyme called a DNA polymerase then guides RNA to the exposed DNA nucleotides. The RNA is primed and another enzyme called Ligase, then seals up the new DNA strand.


Enzymes are protein molecules, and protein molecules are made up from amino acids, and amino acids require DNA in order to be organized into a protein. Take note of how many enzymes were needed in order for the basic action of DNA replication to occur. At least three different enzymes are required (more are actually needed, but for sake of space I’ve condensed the DNA replication process listed here). But here’s the problem; in order to replicate DNA needed to build enzymes, enzymes are needed to replicate.[2] So how could the very first DNA have replicated itself to make enzymes, if enzymes are needed to replicate in the first place?


So just how does the DNA build a protein? Well, first the DNA must be transcribed. Just like replication, the DNA strand is again split and unwound by enzymes. Then comes along Ribosomal RNA which is made up of proteins and RNA. The Ribosomal RNA then takes RNA nucleotides and bonds them to the exposed DNA to form a template. This template strand of RNA can then leave the nucleus of the cell to be translated to build a protein.[3]


Here we find the same problem. In order for transcription to take place to build a protein, proteins are needed to transcribe. How was the first Ribosomal RNA protein built, when the only process that can build it, Transcription, requires a ribosomal RNA already present?


A ribosomal rRNA subunit then attaches to the mRNA, attracting tRNA. The tRNA carries different amino acids based on the code each particular tRNA is. One by one the tRNA match up along the mRNA, fitting like a key in a lock, then they leave behind the particular amino acid they brought with them. The amino acid chain left behind is referred to as a polypeptide chain. This chain of multiple combined amino acids is then folded into a three-dimensional shape by various other proteins called chaperones. Depending on the three dimensional shape it is folded into will determine the function of a brand new protein![4]


So as you can see, the processes of replication, transcription and translation requires the involvement and interaction of various different types of proteins; helicases, chaperones, ribosomal rRNA, etc. But the only way proteins are made is via replication, transcription and translation of DNA followed by proper protein folding by other proteins. So how did proteins come to be, if proteins are needed to have already existed to make other proteins?

Amino Acids and Chiralty

To answer the question of origins we learned that amino acids have been found in various places like on meteorites and have been produced in experiments to simulate the early atmosphere of earth, such as the Miller Urey experiment.[5] The conclusion being that amino acids can form naturally from chemicals, and thus life can form from chemicals (non-life). But recall that even one protein requires a specific combination amino acids, followed by proper folding from other proteins. Without other proteins present how could the amino acid polypeptide chain be folded into a protein? Also, both my textbooks failed to mention that there are over 2,000 amino acids found naturally occurring, but only 20 can be used to build proteins.[6] Were the amino acids from the meteorites and lab experiment the correct 20, or were they just a few of the other 1,980 other amino acids that cannot be used to build a protein?

Furthermore there is an even a greater issue with amino acids called Chiralty. I learned about Chiralty from my personal studies outside of school because it also was not mentioned in either of my biology textbooks. I’ve presented that it takes the proper combination of specific amino acids out of thousands followed by the proper folding of amino acids to create just one protein. But there is a fourth and more important perquisite for amino acids in the polypeptide chain. When the atoms that make up the amino acids fuse together they make two different shaped amino acids, left-handed and right-handed. Just like our two human hands which are completely opposite of each other, amino acids are likewise opposite of each other, mirror like-reflections of one another but not identical, allowing them to fuse together. Interestingly enough when a left-handed amino acid fuses to a right-handed amino acid, they become useless for building a polypeptide chain and therefore useless to building a protein, which is known as being racemic.[7] This phenomenon is called chiralty, which is Greek for handedness.[8]


Here is where it gets interesting; all amino acids used to build proteins in life are all 100% left-handed. There are no right handed amino acids used in life.[9] Equal amounts of left and right handed amino acids called “racemates,” is the product of chemical production of amino acids, which naturally want to bond together. So here are my questions: If all amino acids found chemically are both right-handed and left-handed which naturally want to fuse together making them useless for building proteins, how is it that all proteins found in living organisms have only left-handed amino acids? If life came from non-life, how did the first amino acids, 20 out of 2,000, only left-handed, manage to get in the right combination, and become properly folded to build the first protein?


Law of Biogenesis

Definition: The principle stating that life arises from pre-existing life, not from nonliving material.[10] There are many theories, but facts that cannot be refuted are called laws. Take the law of gravity for example. Life has only been observed forming from other life. If life can arise from non-life it should be doing so frequently to this day and should be observable, yet it is not. If there is no evidence of life arising from non-life, then how can we believe it once did in the past?


Another interesting topic regarding the origin of life is reproduction. The first life form would have to have had the capability to reproduce. Obviously if it did not have the capability to reproduce no subsequent life would follow after it. If it couldn’t reproduce, than life would have to “accidentally” start over again and again. Ultimately, the first life form would have to be capable of reproducing from the beginning. Philosophically speaking, how does an accident in living matter also bring about accidental ability to reproduce itself?

As you can see, when you read just the facts and questions with unbiased it becomes evident that life is incredibly complex, the origins of which (in my opinion) can’t be adequately explained via evolution theory. In my opinion, when one studies biology and genetics, it becomes more and more obvious that life has an immensely complicated design.  Here I believe one can make a teleological argument:

Every design has a designer.

Biological life has a very complex design.

Therefore, biological life had a designer.

This outlook becomes even more solidified when one studies the immense amount of information stored in our DNA. How does chemical accident bring forth intelligent information more complex than any computer code ever created by man? Personally, when I read about these things I can’t help but conclude that there is indeed a God who created us and all of life. But in the meantime, the frog juice… has yet to turn back into a frog.

[1] Ricki Lewis, Human Genetics; Concepts and Applications, (New York:NY McGraw-Hill, 2008) Eighth Edition, Pg. 174.

[2] Ricki Lewis, Human Genetics; Concepts and Applications, (New York:NY McGraw-Hill, 2008) Eighth Edition, Pg. 174.

[3] Ricki Lewis, Human Genetics; Concepts and Applications, (New York:NY McGraw-Hill, 2008) Eighth Edition, Pg. 184.

[4] Ricki Lewis, Human Genetics; Concepts and Applications, (New York:NY McGraw-Hill, 2008) Eighth Edition, Pg. 190.

[5] It should be noted that the meteorites analyzed had of course been in the ground on earth for some time before being analyzed, so finding amino acids on them should not be surprising considering they were probably contaminated while in the ground. Also, the Miller Urey experiment yields multiple flaws outside of the amino acids it produced.

[6] Mike Riddle, The New Answers Book 2, “Can Natural Processes Explain the Origin of Life?” (), Pg. 67.

[7] The definition of racemic;  “of, relating to, or constituting a compound or mixture that is composed of equal amounts of dextrorotatory and levorotatory forms of the same compound and is optically inactive.”, medical dictionary.

[8] Mike Riddle, The New Answers Book 2, “Can Natural Processes Explain the Origin of Life?” (), Pg. 67.

[9] Linus Pauling, General Chemistry, 3rd Edition (San Francisco,CA: W.H. Freeman & Co. 1970) Pr. 774.

The F-22 fighter plane is a highly-sophisticated state of the art military aircraft. It is comprised of thousands of complex parts that all work together to enable the plane to perform a multitude of functions. Individually, these parts cannot operate or fly. But collectively they can fly and execute many different functions.

Now let’s take a hypothetical situation. Let’s imagine the entire earth is covered in huge piles of mechanical parts, thousands and thousands of miles of nothing but pieces of metal, plastic, rubber, etc. Now let’s imagine there are thousands of tornados and hurricanes all over the earth blowing all these parts around and into each other 24-7. Now with all this in mind, do you think it is possible that over the course of thousands or millions or even billions of years, that one of these storms would blow together an F-22 fighter plane in perfect operational condition?

Seems ridiculous right? Given an infinite amount of time, something like this just could not happen…

Now let’s look at the typical human eukaryotic cell. It too, just like the F22, is incredibly sophisticated and complex, but at a much smaller microscopic scale. This cell is also comprised of thousands of working parts (called organelles) that all work together to enable the cell to provide a multitude of functions. Individually, these parts are useless, but collectively they’re necessary. Remove anyone of these important parts and the cell will lose functionality and parish.

So if it is ridiculous to think that a perfectly operational F-22 fighter plane could come into existence via chance, then it is likewise just as illogical to think that such a sophisticated organism could assemble by chance as well. It gets even more absurd to think that this living cell would also form by chance and have the capability to reproduce.

Life cannot come from non-life even if given infinite time and chance. If life could spontaneously generate from non-life than it still should be doing that to this day. However, we’ve never observed it… Hence the Law of Biogenesis: The principle stating that life arises from pre-existing life, not from non-living material.[1] Life is clearly a product of God’s Creation.