Science Disproves Evolution

[Pahu]

Codes, Programs, and Information 1


In our experience, codes are produced only by intelligence, not by natural processes or chance. A code is a set of rules for converting information from one useful form to another. Examples include Morse code and Braille. Code makers must simultaneously understand at least two ways of representing information and then establish the rules for converting from one to the other and back again.

The genetic material that controls the physical processes of life is coded information. Also coded are complex and completely different functions: the transmission, translation, correction, and duplication systems, without which the genetic material would be useless, and life would cease (a). It seems obvious that the genetic code and the accompanying transmission, translation, correction, and duplication systems were produced simultaneously in each living organism by an extremely high intelligence (b).

a. In 2010, another level of complexity was discovered in the genetic code. On a strand of DNA, a sequence of three adjacent nucleotides form a unit in the genetic code called a codon. Prior to 2010, some codons were thought to have the same function as others. That turns out to not be the case.

“...synonymous codon changes can so profoundly change the role of a protein [that it] adds a new level of complexity to how we interpret the genetic code.” Ivana Weygand-Durasevic and Michael Ibba, “New Roles for Codon Usage,” Science, Vol. 329, 17 September 2010, p. 1474. Also see Fangliang Zhang et al., “Differential Arginylation of Actin Isoforms Is Regulated by Coding Sequence-Dependent Degradation,” Science, Vol. 329, 17 September 2010, p. 1734–1537.

b. “Genomes [all the DNA of a species] are remarkable in that they encode most of the functions necessary for their interpretation and propagation.” Anne-Claude Gavin et al., “Proteome Survey Reveals Modularity of the Yeast Cell Machinery,” Nature, Vol. 440, 30 March 2006, p. 631.

c. The genetic code is remarkably insensitive to translation errors. If the code were produced by random processes, as evolutionists believe, life would have needed about a million different starts before a code could have been stumbled on that was as resilient as the code used by all life today. [See Stephen J. Freeland and Laurence D. Hurst, “Evolution Encoded,” Scientific American, Vol. 290, April 2004, pp. 84–91.]

“This analysis gives us a reason to believe that the A–T and G–C choice forms the best pairs that are the most different from each other, so that their ubiquitous use in living things represents an efficient and successful choice rather than an accident of evolution.” [emphasis added] Larry Liebovitch, as quoted by David Bradley, “The Genome Chose Its Alphabet with Care,” Science, Vol. 297, 13 September 2002, p. 1790.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Codes, Programs, and Information 2
​

​

​

No natural process has ever been observed to produce a program. A program is a planned sequence of steps to accomplish some goal. Computer programs are common examples. Because programs require foresight, they are not produced by chance or natural processes. The information stored in the genetic material of all life is a complex program. Therefore, it appears that an unfathomable intelligence created these genetic programs (d).

d. “No matter how many ‘bits’ of possible combinations it has, there is no reason to call it ‘information’ if it doesn’t at least have the potential of producing something useful. What kind of information produces function? In computer science, we call it a ‘program.’ Another name for computer software is an ‘algorithm.’ No man-made program comes close to the technical brilliance of even Mycoplasmal genetic algorithms. Mycoplasmas are the simplest known organisms with the smallest known genome, to date. How was its genome and other living organisms’ genomes programmed?” Abel and Trevors, p. 8.

“No known hypothetical mechanism has even been suggested for the generation of nucleic acid algorithms.” Jack T. Trevors and David L. Abel, “Chance and Necessity Do Not Explain the Origin of Life,” Cell Biology International, Vol. 28, 2004, p. 730.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Codes, Programs, and Information 3


Life contains matter, energy, and information (e).

e. How can we measure information? A computer file might contain information for printing a story, reproducing a picture at a given resolution, or producing a widget to specified tolerances. Information can usually be compressed to some degree, just as the English language could be compressed by eliminating every “u” that directly follows a “q”. If compression could be accomplished to the maximum extent possible (eliminating all redundancies and unnecessary information), the number of bits (0s or 1s) would be a measure of the information needed to produce the story, picture, or widget.

Each living system can be described by its age and the information stored in its DNA. Each basic unit of DNA, called a nucleotide, can be one of four types. Therefore, each nucleotide represents two (log24 = 2) bits of information. Conceptual systems, such as ideas, a filing system, or a system for betting on race horses, can be explained in books. Several bits of information can define each symbol in these books. The number of bits of information, after compression, needed to duplicate and achieve the purpose of a system will be defined as its information content. That number is also a measure of the system’s complexity.

Objects and organisms are not information. Each is a complex combination of matter and energy that the proper equipment—and information—could theoretically produce. Matter and energy alone cannot produce complex objects, living organisms, or information.

While we may not know the precise amount of information in different organisms, we do know those numbers are enormous and quite different. Simply changing (mutating) a few bits to begin the gigantic leap toward evolving a new organ or organism would likely kill the host.

“Information is information, not matter or energy. No materialism which does not admit this can survive at the present day.” Norbert Wiener, Cybernetics; or, Control and Communication in the Animal and the Machine, 2nd edition (Cambridge, Massachusetts: MIT Press, 1948), p. 132.

[From “In the Beginning” by Walt Brown]

 

[lil_christian]

Evolution was disproved long ago. Evolutionists just don't want to admit defeat.

 

[Pahu]

Codes, Programs, and Information 4


All isolated systems, including living organisms, have specific, but perishable, amounts of information. No isolated system has ever been shown to increase its information content significantly (f). Nor do natural processes increase information; they destroy it. Only outside intelligence can significantly increase the information content of an otherwise isolated system. All scientific observations are consistent with this generalization, which has three corollaries:

Macroevolution cannot occur (g).
Outside intelligence was involved in the creation of the universe and all forms of life (h).
Life could not result from a “big bang” (i).

f. Werner Gitt (Professor of Information Systems) describes man as the most complex information processing system on earth. Gitt estimated that about 3×10^24 bits of information are processed daily in an average human body. That is thousands of times more than all the information in all the world’s libraries. [See Werner Gitt, In the Beginning Was Information, 2nd edition (Bielefeld, Germany: CLV, 2000), p. 88.]

“There is no known law of nature, no known process and no known sequence of events which can cause information to originate by itself in matter.” Ibid., p. 107.

g. Because macroevolution requires increasing complexity through natural processes, the organism’s information content must spontaneously increase many times. However, natural processes cannot significantly increase the information content of an isolated system, such as a reproductive cell. Therefore, macroevolution cannot occur.

“The basic flaw of all evolutionary views is the origin of the information in living beings. It has never been shown that a coding system and semantic information could originate by itself in a material medium, and the information theorems predict that this will never be possible. A purely material origin of life is thus precluded.” Gitt, p. 124.

h. Based on modern advances in the field of information theory, the only known way to decrease the entropy of an isolated system is by having intelligence in that system. [See, for example, Charles H. Bennett, “Demons, Engines and the Second Law,” Scientific American, Vol. 257, November 1987, pp. 108–116.] Because the universe is far from its maximum entropy level, a vast intelligence is the only known means by which the universe could have been brought into being. [See also “Second Law of Thermodynamics” ]

i. If the “big bang” occurred, all the matter in the universe was at one time a hot gas. A gas is one of the most random systems known to science. Random, chaotic movements of gas molecules contain virtually no useful information. Because an isolated system, such as the universe, cannot generate nontrivial information, the “big bang” could not produce the complex, living universe we have today, which contains astronomical amounts of useful information.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Compatible Senders and Receivers


Only intelligence creates codes, programs, and information (CP&I). Each involves senders and receivers. Senders and receivers can be people, animals, plants, organs, cells, or certain molecules. (The DNA molecule is a prolific sender.) The CP&I in a message must be understandable and beneficial to both sender and receiver; otherwise, the effort expended in transmitting and receiving messages (written, chemical, electrical, magnetic, visual, and auditory) will be wasted.

Consider the astronomical number of links (message channels) that exist between potential senders and receivers: from the cellular level to complete organisms, from bananas to bacteria to babies, and across all of time since life began. All must have compatible understandings (CP&I) and equipment (matter and energy). Designing compatibilities of this magnitude requires one or more superintelligences who completely understand how matter and energy behave over time. In other words, the superintelligence(s) must have made, or at least mastered, the laws of chemistry and physics wherever senders and receivers are found. The simplest, most parsimonious way to integrate all of life is for there to be only one superintelligence.

Also, the sending and receiving equipment, including its energy sources, must be in place and functional before communication begins. But the preexisting equipment provides no benefit until useful messages begin arriving. Therefore, intelligent foresight (planning) is mandatory—something nature cannot do.

[From “In the Beginning” by Walt Brown]

 

[HeIsNowHere]

Perhaps I may shed some light onto your post.



While what you are saying is true, you're leaving out some vital information. In the example, it's true that the man with the large muscles won't pass his large muscles on to his offspring. The evolutionary characteristic that he passes down to his offspring is the genetic potential for large muscles. Over time, the need to develop large muscles in order to survive tweaks the man's ancestors' bodies in such a way that they are better adapted to maintain large muscles (such as passing down high metabolism). In the same way, no evolutionist is honestly claiming that a primitive short-necked giraffe-like creature began to stretch it's neck out and then it's offspring began to do the same. As you well know, parents pass on physical genetic traits to their offspring. That's the reason why children tend to look like their parents. These physical traits include eye color, nose curvature, bone structure, and yes, even neck length. Natural selection claims that giraffes have long necks because as some point in their ancestral past, there was a food crisis. During this food crisis, most of the foliage which these creatures needed to survive could be reached only by individuals whose neck stretched high enough to grab it. Since the individuals born with the slightly longer necks were the only ones receiving nutrition, the short-neck gene eventually died off. Let's say, for instance, that the neck length of this creature ranged from 10 cm to 15 cm. During this hypothesized (and archaeologically supported) period of a food crisis, the foliage was only available to a creature with a neck size of 14 cm and higher (of course the numbers are arbitrary because I made them up for the metaphor, but surely you follow). Since only the creatures with necks 14 cm or higher are able to obtain food, they are the only ones who are able to pass their genes on to a new generation. In this new generation, all of the creatures have necks ranging somewhere within the general range of 14 cm to 15 cm. Another characteristic that is passed down is the potential to stretch the neck a little higher in case there is a need for food on even higher branches. Though acquired characteristics are not handed down genetically, their potential is.

Perhaps that clarified a few things.

When you state that there is "potential" you have gone from observable science to belief. What is the empirical evidence for "potential". The fact of selection from a Biblical creation perspective is was written long before Darwin by Creationist Edward Blythe. The Creator has created within kinds ability to adapt to differing environments on earth. That fact is not denied and is supported by breeding. However, this process does not add information content to the genome and at best mutations (the mechanism that supposedly creates "potential") can only rearrange information. There is NEVER any mechanism that has been observed to add information to the set of genes between kinds. Universal information is the achilles heel of the GTE (general theory of evolution). If you read Dr. Werner Gitt's 2nd book on the scientific laws of information found in the book "Without Excuse" you will discover natural laws disproving the GTE and proving a Creator of life who is a genius of geniuses. Where did the coded information in life come from? If a simple 1st life evolved with complete coded information, and all of the other vast numbers of required bio-machinery even for the simplest of creatures, where or how did information content increase to make the next higher order creature? Evolution or the GTE is based on an anti-Creator religion of naturalism and pure beliefs. Words such as "potential" are simply wishful thinking. The fact is the Bible is the expired Word of God and Genesis as history was expired from God to Moses live on the Mountain over 40 days and then Moses wrote it for us. "The fear (respect) of God is the beginning of Wisdom" "The fool has said in his heart there is no God". We are barraged by so many fools who speak well and tell clever stories that sound like "fact" but are actually religious propoganda of the anti-Creator religion.

 

[Pahu]

The fact is the Bible is the expired Word of God and Genesis as history was expired from God to Moses live on the Mountain over 40 days and then Moses wrote it for us. "The fear (respect) of God is the beginning of Wisdom" "The fool has said in his heart there is no God". We are barraged by so many fools who speak well and tell clever stories that sound like "fact" but are actually religious propoganda of the anti-Creator religion.

Did you mean to say inspired rather than expired? I hope that wasn't a Freudian Slip.

 

[Pahu]

Convergent Evolution or Intelligent Design? 1


When the same complex capability is found in unrelated organisms but not in their alleged evolutionary ancestors, evolutionists say that a common need caused identical complexities to evolve. They call this convergent evolution.

For example, wings and flight occur in some birds, insects, and mammals (bats). Pterosaurs, an extinct reptile, also had wings and could fly. These capabilities have not been found in any of their alleged common ancestors. Other examples of convergent evolution are the three tiny bones in the ears of mammals: the stapes, incus, and malleus. Their complex arrangement and precise fit give mammals the unique ability to hear a wide range of sounds. Evolutionists say that those bones evolved from bones in a reptile’s jaw. If so, the process must have occurred at least twice (a)—but left no known transitional fossils. How did the transitional organisms between reptiles and mammals hear during those millions of years (b)? Without the ability to hear, survival—and reptile-to-mammal evolution—would cease.

Concluding that a miracle—or any extremely unlikely event—happened once requires strong evidence or faith; claiming that a similar “miracle” happened repeatedly requires either incredible blind faith or a cause common to each event, such as a common designer.

a. “...the definitive mammalian middle ear evolved independently in living monotremes and therians (marsupials and placentals).” Thomas H. Rich et al., “Independent Origins of Middle Ear Bones in Monotremes and Therians,” Science, Vol. 307, 11 February 2005, p. 910.

“Because of the complexity of the bone arrangement, some scientists have argued that the innovation arose just once—in a common ancestor of the three mammalian groups. Now, analyses of a jawbone from a specimen of Teinolophos trusleri, a shrew-size creature that lived in Australia about 115 million years ago, have dealt a blow to that notion.” Sid Perkins, “Groovy Bones,” Science News, Vol. 167, 12 February 2005, p. 100.

b. Also, for mammals to hear also requires the organ of Corti and complex “wiring” in the brain. No known reptile (the supposed ancestor of mammals), living or fossil, has anything resembling this amazing organ.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Convergent Evolution or Intelligent Design? 2


It is illogical to maintain that similarities between different forms of life always imply a common ancestor (c); such similarities may imply a common designer and show efficient design. In fact, where similar structures are known to be controlled by different genes (d) or are developed from different parts of embryos (e), a common designer is a much more likely explanation than evolution.

c. “By this we have also proved that a morphological similarity between organisms cannot be used as proof of a phylogenetic [evolutionary] relationship...it is unscientific to maintain that the morphology may be used to prove relationships and evolution of the higher categories of units...” Nilsson, p. 1143.

“But biologists have known for a hundred years that homologous [similar] structures are often not produced by similar developmental pathways. And they have known for thirty years that they are often not produced by similar genes, either. So there is no empirically demonstrated mechanism to establish that homologies are due to common ancestry rather than common design.” Jonathan Wells, “Survival of the Fakest,” The American Spectator, December 2000/January 2001, p. 22.

d. Fix, pp. 189–191.

Denton, pp. 142–155.

“Therefore, homologous structures need not be controlled by identical genes, and homology of phenotypes does not imply similarity of genotypes. [emphasis in original] It is now clear that the pride with which it was assumed that the inheritance of homologous structures from a common ancestor explained homology was misplaced; for such inheritance cannot be ascribed to identity of genes. ... But if it is true that through the genetic code, genes code for enzymes that synthesize proteins which are responsible (in a manner still unknown in embryology) for the differentiation of the various parts in their normal manner, what mechanism can it be that results in the production of homologous organs, the same ‘patterns’, in spite of their not being controlled by the same genes? I asked this question in 1938, and it has not been answered.” [Nor has it been answered today.] Gavin R. deBeer, formerly Professor of Embryology at the University of London and Director of the British Museum (Natural History), Homology, An Unsolved Problem (London: Oxford University Press, 1971), p. 16.

e. “Structures as obviously homologous as the alimentary canal in all vertebrates can be formed from the roof of the embryonic gut cavity (sharks), floor (lampreys, newts), roof and floor (frogs), or from the lower layer of the embryonic disc, the blastoderm, that floats on the top of heavily yolked eggs (reptiles, birds). It does not seem to matter where in the egg or the embryo the living substance out of which homologous organs are formed comes from. Therefore, correspondence between homologous structures cannot be pressed back to similarity of position of the cells of the embryo or the parts of the egg out of which these structures are ultimately differentiated.” [emphasis in original] Ibid., p. 13.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Vestigial Organs


Some structures in humans were once thought to have no function but to have been derived from functioning organs in claimed evolutionary ancestors (a). They were called vestigial organs. As medical knowledge has increased, at least some function has been discovered for all alleged vestigial organs (b). For example, the human appendix was once considered a useless remnant from our evolutionary past. The appendix plays a role in antibody production, protects part of the intestine from infections and tumor growths (c), and safely stores “good bacteria” that can replenish the intestines following bouts of diarrhea, for example (d). Indeed, the absence of true vestigial organs implies evolution never happened.

a. “The existence of functionless ‘vestigial organs’ was presented by Darwin, and is often cited by current biology textbooks, as part of the evidence for evolution....An analysis of the difficulties in unambiguously identifying functionless structures and an analysis of the nature of the argument, leads to the conclusion that ‘vestigial organs’ provide no evidence for evolutionary theory.” S. R. Scadding, “Do ‘Vestigial Organs’ Provide Evidence for Evolution?” Evolutionary Theory, Vol. 5, No. 3, May 1981, p. 173.

b. Jerry Bergman and George Howe, “Vestigial Organs” Are Fully Functional (Terre Haute, Indiana: Creation Research Society Books, 1990).

c. “The appendix is not generally credited with substantial function. However, current evidence tends to involve it in the immunologic mechanism.” Gordon McHardy, “The Appendix,” Gastroenterology, Vol. 4, editor J. Edward Berk (Philadelphia: W. B. Saunders Co., 1985), p. 2609.

“Thus, although scientists have long discounted the human appendix as a vestigial organ, a growing quantity of evidence indicates that the appendix does in fact have a significant function as a part of the body’s immune system. ” N. Roberts, “Does the Appendix Serve a Purpose in Any Animal?” Scientific American, Vol. 285, November 2001, p. 96.

d. “...the human appendix is well suited as a ‘safe house’ for commensal bacteria, providing support for bacterial growth and potentially facilitating re-inoculation of the colon in the event that the contents of the intestinal track are purged following exposure to a pathogen....the appendix...is not a vestige.” R. Randal Bollinger et. al., “Biofilms in the Large Bowel Suggest an Apparent Function of the Human Vermiform Appendix,” Journal of Theoretical Biology, Vol. 249, 2007, p. 826.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Two-Celled Life?
​

​

​

Many single-celled forms of life exist, but no known forms of animal life have 2, 3, 4, or 5 cells (a). Known forms of life with 6–20 cells are parasites, so they must have a complex animal as a host to provide such functions as respiration and digestion. If macroevolution happened, one should find many transitional forms of life with 2–20 cells—filling the gap between one-celled and many-celled organisms.

a. E. Lendell Cockrum and William J. McCauley, Zoology (Philadelphia: W. B. Saunders Co., 1965), p. 163.

Lynn Margulis and Karlene V. Schwartz, Five Kingdoms: An Illustrated Guide to the Phyla of Life on Earth (San Francisco: W. H. Freeman and Co., 1982), pp. 178–179.

Perhaps the simplest forms of multicellular life are the Myxozoans, which have 6–12 cells. While they are quite distinct from other multicellular life, they are even more distinct from single-celled life (kingdom Protista). [See James F. Smothers et al., “Molecular Evidence That the Myxozoan Protists are Metazoans,” Science, Vol. 265, 16 September 1994, pp. 1719–1721.] So, if they evolved from anywhere, it would most likely have been from higher, not lower, forms of life. Such a feat should be called devolution, not evolution.

Colonial forms of life are an unlikely bridge between single-celled life and multicelled life. The degree of cellular differentiation between colonial forms of life and the simplest multicellular forms of life is vast. For a further discussion, see Libbie Henrietta Hyman, The Invertebrates: Protozoa through Ctenophora, Vol. 1 (New York: McGraw-Hill, 1940), pp. 248–255.

Nor do Diplomonads (which have two nuclei and four flagella) bridge the gap. Diplomonads are usually parasites.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Embryology 1


Evolutionists have taught for over a century that as an embryo develops, it passes through stages that mimic an evolutionary sequence. In other words, in a few weeks an unborn human repeats stages that supposedly took millions of years for mankind. A well-known example of this ridiculous teaching is that embryos of mammals have “gill slits,” because mammals supposedly evolved from fish. (Yes, that’s faulty logic.) Embryonic tissues that resemble “gill slits” have nothing to do with breathing; they are neither gills nor slits. Instead, those embryonic tissues develop into parts of the face, bones of the middle ear, and endocrine glands.

Embryologists no longer consider the superficial similarities between a few embryos and the adult forms of simpler animals as evidence for evolution (a).

a. “This generalization was originally called the biogenetic law by Haeckel and is often stated as ‘ontogeny [the development of an embryo] recapitulates [repeats] phylogeny [evolution].’ This crude interpretation of embryological sequences will not stand close examination, however. Its shortcomings have been almost universally pointed out by modern authors, but the idea still has a prominent place in biological mythology.” Paul R. Ehrlich and Richard W. Holm, The Process of Evolution (New York: McGraw-Hill, 1963), p. 66.

“It is now firmly established that ontogeny does not repeat phylogeny.” George Gaylord Simpson and William S. Beck, Life: An Introduction to Biology (New York: Harcourt, Brace & World, Inc., 1965), p. 241.

Hitching, pp. 202–205.

“The enthusiasm of the German zoologist, Ernst Haeckel, however, led to an erroneous and unfortunate exaggeration of the information which embryology could provide. This was known as the ‘biogenetic law’ and claimed that embryology was a recapitulation of evolution, or that during its embryonic development an animal recapitulated the evolutionary history of its species.” Gavin R. deBeer, An Atlas of Evolution (New York: Nelson, 1964), p. 38.

“...the theory of recapitulation has had a great and, while it lasted, regrettable influence on the progress of embryology.” Gavin R. deBeer, Embryos and Ancestors, revised edition (London: Oxford University Press, 1951), p. 10.

“Moreover, the biogenetic law has become so deeply rooted in biological thought that it cannot be weeded out in spite of its having been demonstrated to be wrong by numerous subsequent scholars.” Walter J. Bock, “Evolution by Orderly Law,” Science, Vol. 164, 9 May 1969, pp. 684–685.

“...we no longer believe we can simply read in the embryonic development of a species its exact evolutionary history.” Hubert Frings and Marie Frings, Concepts of Zoology (Toronto: Macmillan Publishing Co., 1970), p. 267.

“The type of analogical thinking which leads to theories that development is based on the recapitulation of ancestral stages or the like no longer seems at all convincing or even interesting to biologists.” Conrad Hal Waddington, Principles of Embryology (London: George Allen and Unwin Ltd., 1956), p. 10.

“Surely the biogenetic law is as dead as a doornail.” Keith Stewart Thomson, “Ontogeny and Phylogeny Recapitulated,” American Scientist, Vol. 76, May–June 1988, p. 273.

“The biogenetic law—embryologic recapitulation—I think, was debunked back in the 1920s by embryologists.” David Raup, as taken from page 16 of an approved and verified transcript of a taped interview conducted by Luther D. Sunderland on 27 July 1979. [See also Luther D. Sunderland, Darwin’s Enigma (San Diego: Master Book Publishers, 1984), p. 119.]

“The theory of recapitulation was destroyed in 1921 by Professor Walter Garstang in a famous paper. Since then no respectable biologist has ever used the theory of recapitulation, because it was utterly unsound, created by a Nazi-like preacher named Haeckel.” Ashley Montagu, as quoted by Sunderland, p. 119.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Embryology 2


Ernst Haeckel, by deliberately falsifying his drawings (b), originated and popularized this incorrect but widespread belief [of the “biogenetic law”]. Many modern textbooks continue to spread this false idea as evidence for evolution (c).

b. Haeckel, who in 1868 advanced this “biogenetic law” that was quickly adopted in textbooks and encyclopedias worldwide, distorted his data. Thompson explains:

“A natural law can only be established as an induction from facts. Haeckel was of course unable to do this. What he did was to arrange existing forms of animal life in a series proceeding from the simple to the complex, intercalating [inserting] imaginary entities where discontinuity existed and then giving the embryonic phases names corresponding to the stages in his so-called evolutionary series. Cases in which this parallelism did not exist were dealt with by the simple expedient of saying that the embryological development had been falsified. When the ‘convergence’ of embryos was not entirely satisfactory, Haeckel altered the illustrations of them to fit his theory. The alterations were slight but significant. The ‘biogenetic law’ as a proof of evolution is valueless.” W. R. Thompson, p. 12.

“To support his case he [Haeckel] began to fake evidence. Charged with fraud by five professors and convicted by a university court at Jena, he agreed that a small percentage of his embryonic drawings were forgeries; he was merely filling in and reconstructing the missing links when the evidence was thin, and he claimed unblushingly that ‘hundreds of the best observers and biologists lie under the same charge.’” Pitman, p. 120.

M. Bowden, Ape-Men: Fact or Fallacy? 2nd edition (Bromley, England: Sovereign Publications, 1981), pp. 142–143.

Wilbert H. Rusch, Sr., “Ontogeny Recapitulates Phylogeny,” Creation Research Society Quarterly, Vol. 6, June 1969, pp. 27–34.

“...ontogeny recapitulates phylogeny, meaning that in the course of its development [ontogeny] an embryo recapitulates [repeats] the evolutionary history of its species [phylogeny]. This idea was fathered by Ernst Haeckel, a German biologist who was so convinced that he had solved the riddle of life’s unfolding that he doctored and faked his drawings of embryonic stages to prove his point.” Fix, p. 285.

“[The German scientist Wilhelm His] accused Haeckel of shocking dishonesty in repeating the same picture several times to show the similarity among vertebrates at early embryonic stages in several plates of [Haeckel’s book].” Stephen Jay Gould, Ontogeny and Phylogeny (Cambridge, Massachusetts: The Belknap Press of Harvard University Press, 1977), p. 430.

“It looks like it’s turning out to be one of the most famous fakes in biology.” Michael K. Richardson, as quoted by Elizabeth Pennisi, “Haeckel’s Embryos: Fraud Rediscovered,” Science, Vol. 277, 5 September 1997, p. 1435.

“When we compare his [Haeckel’s] drawings of a young echidna embryo with the original, we find that he removed the limbs (see Fig. 1). This cut was selective, applying only to the young stage. It was also systematic because he did it to other species in the picture. Its intent is to make the young embryos look more alike than they do in real life.” Michael K. Richardson and Gerhard Keuck, “A Question of Intent: When Is a ‘Schematic’ Illustration a Fraud?” Nature, Vol. 410, 8 March 2001, p. 144.

c. “Another point to emerge from this study is the considerable inaccuracy of Haeckel’s famous figures. These drawings are still widely reproduced in textbooks and review articles, and continue to exert a significant influence on the development of ideas in this field.” Michael K. Richardson et al., “There Is No Highly Conserved Embryonic Stage in the Vertebrates,” Anatomy and Embryology, Vol. 196, No. 2, August 1997, p. 104.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Rapid Burial


Rapid Burial


Fossils all over the world show evidence of rapid burial. Many fossils, such as fossilized jellyfish (a), show by the details of their soft, fleshy portions (b) that they were buried rapidly, before they could decay. (Normally, dead animals and plants quickly decompose.) The presence of fossilized remains of many other animals, buried in mass graves and lying in twisted and contorted positions, suggests violent and rapid burials over large areas (c). These observations, together with the occurrence of compressed fossils and fossils that cut across two or more layers of sedimentary rock, are strong evidence that the sediments encasing these fossils were deposited rapidly—not over hundreds of millions of years. Furthermore, almost all sediments that formed today’s rocks were sorted by water. The worldwide fossil record is, therefore, evidence of rapid death and burial of animal and plant life by a worldwide, catastrophic flood. The fossil record is not evidence of slow change (d).

Figure 7: Fossil of Fish Swallowing Fish. The fossilization process must have been quite rapid to have preserved a fish in the act of swallowing another fish. Thousands of such fossils have been found.

Figure 8: Fish in Long Fish. In the belly of the above 14-foot-long fish is a smaller fish, presumably the big fish’s breakfast. Because digestion is rapid, fossilization must have been even more so.

Figure 9: Fish in Curved Fish. The curved back shows that this fish died under stress.

Figure 10: Dragonfly Wing. This delicate, 1 1/2-foot-long wing must have been buried rapidly and evenly to preserve its details. Imagine the size of the entire dragonfly!

a. Thousands of jellyfish, many bigger than a dinner plate, are found in at least seven different horizons of coarse-grained, abrasive sandstone in Wisconsin. [See James W. Hagadorn et al., “Stranded on a Late Cambrian Shoreline: Medusae from Central Wisconsin,” Geology, Vol. 30, No. 2, February 2002, pp. 147–150.]

Coarse grains slowly covering a jellyfish would allow atmospheric oxygen to migrate in and produce rapid decay. Burial in clay or mud would better shield an organism from decay. If coarse-grain sand buried these jellyfish in a storm, turbulence and abrasion by the sand grains would tear and destroy the jellyfish. To understand how thousands of jellyfish were gently collected and preserved in coarse-grained sand, see pages [178-189 ].

Charles Darwin recognized the problem of finding fossilized soft-bodied organisms such as jellyfish. He wrote:

“No organism wholly soft can be preserved.” Charles Darwin, The Origin of Species, p. 330.

Once again, a prediction of evolution is seen to be wrong.

Preston Cloud and Martin F. Glaessner, “The Ediacarian Period and System: Metazoa Inherit the Earth,” Science, Vol. 217, 27 August 1982, pp. 783–792. [See also the cover of that issue.]

Martin F. Glaessner, “Pre-Cambrian Animals,” Scientific American, Vol. 204, March 1961, pp. 72–78.

b. Donald G. Mikulic et al., “A Silurian Soft-Bodied Biota,” Science, Vol. 228, 10 May 1985, pp. 715–717.

“...preconditions for the preservation of soft-bodied faunas: rapid burial of fossils in undisturbed sediment; deposition in an environment free from the usual agents of immediate destruction—primarily oxygen and other promoters of decay, and the full range of organisms, from bacteria to large scavengers, that quickly reduce most carcasses to oblivion in nearly all earthly environments; and minimal disruption by the later ravages of heat, pressure, fracturing, and erosion....But the very conditions that promote preservation also decree that few organisms, if any, make their natural homes in such places.” Stephen Jay Gould, Wonderful Life (New York: W. W. Norton & Co., 1989), pp. 61–62.

c. Presse Grayloise, “Very Like a Whale,” The Illustrated London News, 1856, p. 116.

Sunderland, pp. 111–114.

David Starr Jordan, “A Miocene Catastrophe,” Natural History, Vol. 20, January–February 1920, pp. 18–22.

Hugh Miller, The Old Red Sandstone, or New Walks in an Old Field (Boston: Gould and Lincoln, 1858), pp. 221–225.

d. Harold G. Coffin, Origin By Design (Washington, D.C.: Review and Herald Publishing Assn., 1983), pp. 30–40.

[From “In the Beginning” by Walt Brown]

 

[akirarene]

I ended up not reading anything u wrote instead I saw like "AAAAAAAAAAAAAAWWWWWWWWWWWWWWWWW" THE middle one looks like my doggie XD

 

[Pahu]

Parallel Strata

The earth’s sedimentary layers are typically parallel to adjacent layers. Such uniform layers are seen, for example, in the Grand Canyon and in road cuts in mountainous terrain. Had these parallel layers been deposited slowly over thousands of years, erosion would have cut many channels in the topmost layers. Their later burial by other sediments would produce nonparallel patterns. Because parallel layers are the general rule, and the earth’s surface erodes rapidly, one can conclude that almost all sedimentary layers were deposited rapidly relative to the local erosion rate—not over long periods of time (The mechanism involved is explained on pages 178-189 ).

Figure 11: Polystrate Fossil. Fossils crossing two or more sedimentary layers (strata) are called poly- (many) strate (strata) fossils. Consider how quickly this tree trunk in Germany must have been buried. Had burial been slow, the tree top would have decayed. Obviously, the tree could not have grown up through the strata without sunlight and air. The only alternative is rapid burial. Some polystrate trees are upside down, which could occur in a large flood. Soon after Mount St. Helens erupted in 1980, scientists saw trees being buried in a similar way in the lake-bottom sediments of Spirit Lake. Polystrate tree trunks are found worldwide. (Notice the 1-meter scale bar, equal to 3.28 feet, in the center of the picture.)

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Fossil Gaps 1


If evolution happened, the fossil record should show continuous and gradual changes from the bottom to the top layers. Actually, many gaps or discontinuities appear throughout the fossil record (a).

a. “But, as by this theory innumerable transitional forms must have existed, why do we not find them imbedded in countless numbers in the crust of the earth?” Darwin, The Origin of Species, p. 163.

“...the number of intermediate varieties, which have formerly existed [must] truly be enormous. Why then is not every geological formation and every stratum full of such intermediate links? Geology assuredly does not reveal any such finely-graduated organic chain; and this, perhaps, is the most obvious and serious objection which can be urged against the theory [of evolution].” Ibid., p. 323.

Darwin then explained that he thought that these gaps existed because of the “imperfection of the geologic record.” Early Darwinians expected the gaps would be filled as fossil exploration continued. Most paleontologists now agree that this expectation has not been fulfilled.

[From “In the Beginning” by Walt Brown]

 

[Pahu]

Fossil Gaps 2


The Field Museum of Natural History in Chicago has one of the largest collections of fossils in the world. Consequently, its former dean, Dr. David Raup, was highly qualified to discuss the absence of transitions in the fossil record:

“Well, we are now about 120 years after Darwin and the knowledge of the fossil record has been greatly expanded. We now have a quarter of a million fossil species bu
t the situation hasn’t changed much. The record of evolution is still surprisingly jerky and, ironically, we have even fewer examples of evolutionary transition than we had in Darwin’s time. By this I mean that some of the classic cases of Darwinian change in the fossil record, such as the evolution of the horse in North America, have had to be discarded or modified as a result of more detailed information—what appeared to be a nice simple progression when relatively few data were available now appears to be much more complex and much less gradualistic. So Darwin’s problem has not been alleviated in the last 120 years and we still have a record which does show change but one that can hardly be looked upon as the most reasonable consequence of natural selection.” David M. Raup, “Conflicts Between Darwin and
Paleontology,” Field Museum of Natural History Bulletin, Vol. 50, No. 1, January 1979, p. 25.

“Surely the lack of gradualism—the lack of intermediates—is a major problem.” Dr. David Raup, as taken from page 16 of an approved and verified transcript of a taped interview conducted by Luther D. Sunderland on 27 July 1979.

“In fact, the fossil record does not convincingly document a single transition from one species to another.” Stanley, p. 95.

“But fossil species remain unchanged throughout most of their history and the record fails to contain a single example of a significant transition.” David S. Woodruff, “Evolution: The Paleobiological View,” Science, Vol. 208, 16 May 1980, p. 716.

[From “In the Beginning” by Walt Brown]

 

[Dude653]

I have no interest in a science that teaches a theory that has been proven to be mathematicaly impossible. I'm not intersted in a science that carbon dated a live penguin to be 1000 yrs old