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Friday, September 30, 2022

Australia's Unique Animals

 

Australia's Unique Animals

Q.

How do creationists explain the origin and distribution of Australia’s unique animals in terms of a young Earth and a worldwide flood?

A.

Explaining the origin of Australia’s marsupial population, and especially its uniqueness to that one isolated southern continent, is difficult for evolutionists and creationists alike. Marsupials such as kangaroos, opossums, wallabies, and koalas seem unusual, but monotremes (i.e., the echidna and the platypus) are even more puzzling. The main difference between marsupials and most other mammals' centers on the reproductive system. Marsupials give birth prematurely and allow the fetus to develop in an external pouch. In other mammals, excluding the monotremes which lay eggs, the fetus develops within the uterus and is attached to, and nourished by, the placenta.

Perhaps the most interesting fact about marsupials is that they nearly all have non-marsupial equivalents in other parts of the world (see Dobzhansky, et al., 1977, Figure 9.3, p. 267). The kangaroo has a similar role to the antelope roaming the African savanna. The wombat resembles a badger, and even has a backward-pointing pouch so that it will not fill with dirt while burrowing! There also are many small marsupials that have rodent counterparts. Evolutionists attribute such similarities to “parallel evolution” in both homology (being alike in form) and analogy (occupying a corresponding niche). That is, they believe that these marsupials and their placental peers developed independently; they share similar characteristics, but took two different paths to get there (see Simpson and Beck, 1965, pp. 499-501). A common ancestry, combined with similar forces of natural selection, evolutionists assert, will result in the same sort of changes through time. This common ancestor is thought to be the opossum because it is a marsupial and is found in other areas of the world apart from Australia.

According to evolutionary theory, the opossum was a primitive mammal living 200 million years ago on a single southern land mass called Gondwanaland. When parts of this supercontinent divided into what are now Australia and South America, the opossums were separated geographically. Over eons of time, so the story goes, the Australian descendants of the opossum developed into the various types of marsupials seen today. However, in South America, they “evolved” placentas and eventually migrated to North America and Eurasia.

These evolutionary ideas suffer from a number of problems, as listed below:

  • There are no intermediate fossils (“transitional forms”) showing the development of the various marsupials from an opossum or opossum-like ancestor. Further, to suggest that one type of mammal could arise by supposed evolutionary mechanisms is incredible enough, but the chances of having both placental and non-placental forms evolve in the same way, at the same time, and in different regions, are remote to say the least.
     
  • The humble opossum has been nominated as the ancestor of all mammals because it is supposed to be so “primitive,” having a relatively small brain and no “specialized” characteristics. But the opossum has thrived virtually unchanged in many parts of the world. In general, marsupials often are considered less “advanced” because they lack the complex internal reproductive system of placental mammals. However, they possess many other characteristics that could give them an edge over their placental counterparts. For instance, a female kangaroo can nourish two young ones of different ages at the same time, providing the appropriate formula from each teat. Unlike placental mammals, marsupials can suspend or abort the embryo deliberately if adverse conditions arise. And, of course, the pouch provides a superior place of protection for the young marsupial. Yes, marsupials are different, but they are not inferior.
     
  • The distribution of marsupials is not well-answered by evolutionary theories. According to Michael Pitman, “the most diverse fossil assemblies have been obtained from South America and, later (Pliocene), Australia” (1984, p. 206). That is, according to the fossil record, the marsupials already were well-defined as a distinct group before the separation of Australia from other continents. Thus, geographic separation cannot be as significant to their development as evolutionists like to think. An alternate, biblically based model is as follows:

    1. It is reasonable to suggest that God created the various kinds of marsupials. Hence, the many varieties of opossums, kangaroos, wallabies, and so on, most likely have arisen since the time of creation.
       
    2. There could be any number of reasons that God created both placental and non-placental forms. One possibility is that marsupials were created for a specific environment. For example, on the African savannas or North American plains, animals migrate to different areas according to the seasons, and range over huge tracts of land in search of better grazing. However, vegetation patterns in Australia do not allow such flexibility. The unique characteristics of marsupials that allow them to survive in a tough environment are indicative of good design, not blind evolution.
       
    3. Representatives of marsupial kinds went into the ark and were carried through the Flood. Any other varieties not in the ark became extinct with the Flood (and now exist only as fossils).
       
    4. After the Flood, marsupials may have migrated to Australia across land connections or narrow waterways. Perhaps there is a supernatural element involving the second point made above. That is, God, having created specially equipped creatures, may have directed them to settle in Australia in particular. If God can arrange for all the animals to go to Noah (Genesis 6:20), then He very well could assist and direct them in their migration from Ararat once they left the ark (Genesis 8:17).
       
    5. There is no need to postulate long periods of time for whole-scale movement of animal kinds over the Earth. Initial studies by Richard Culp show that there are minimal differences between many North American, European, and Asian varieties of certain plant and animal species (Culp, 1988). The lack of dissimilarities, and the occurrence of unique animal or plant assemblages in various parts of the world (not just Australia), may be evidence for a rapid resettlement in relatively recent times. This would be consistent with the Genesis account.

    REFERENCES

    Bartz, Paul A. (1989), “Questions and Answers,” Bible-Science Newsletter, 27[7]:12, July.

    Culp, G. Richard (1988), “The Geographical Distribution of Animals and Plants,” Creation Research Society Quarterly, 25[1]:24-27, June.

    Dobzhansky, Theodosius, F.J. Ayala, G.L. Stebbins, and J.W. Valentine (1977), Evolution (San Francisco, CA: W.H. Freeman).

    Pitman, Michael (1984), Adam and Evolution (London: Rider).

    Simpson, G.G. and W.S. Beck (1965), Life: An Introduction to Biology (New York: Harcourt, Brace & World), second edition.

     

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Thursday, September 29, 2022

Who Is This "Eve"?

 

Who Is This "Eve"?

A scientific “discovery” has captured the attention of the popular press. It seems scientists have “proven” that all modern human beings can trace their ancestry back to one woman living 200,000 years ago in Africa (Cann, et al., 1987). This one woman was nicknamed “Eve”—much to the media’s delight. An article in the January 1987 issue of Time magazine was headed, “Everyone’s Genealogical Mother: Biologists Speculate that ‘Eve’ Lived in Sub-Saharan Africa” (Lemonick, 1987). A year later, that “speculation” became a major Newsweek production titled “The Search for Adam and Eve” (Tierney, et al., 1988). The provocative front cover presented a snake, tree, and nude African couple in a “Garden of Eden” setting. The Bible-story imagery was reinforced by showing the woman offering an apple to the man.

Many people latched onto these findings as proof of the biblical record. After all, didn’t they prove what the Bible has always taught—that Eve was the first woman? Others have seen the story for what it is: media hype over a new twist in evolutionary thinking encumbered with questionable assumptions. After some background discussion, several difficulties with the evolutionary “Eve” hypothesis will be presented.

MAKING OUR FAMILY TREE

Two questions come to mind in responding to the researchers’ claims described above. First, how can they say that our common ancestor was a woman living in Africa? And second, how can they say she lived around 200,000 years ago?

A Female Prerogative

The genetic material in the cell nucleus, with its DNA code, controls the functions of the cell, bringing in nutrients from the body, and making hormones, proteins, and other chemicals. Outside the nucleus is an area called the cytoplasm which contains, among other things, tiny bean-shaped objects called mitochondria. These are often described as the “energy factories” of the cell.

Mitochondria have their own DNA which is used to make some of the mitchondrion’s proteins; the nuclear DNA does the rest. The mitchondrial DNA (or mtDNA) is special for two reasons. First, it is short and simple in comparison to the nuclear DNA, containing only thirty-seven genes instead of around 30,000 genes. This makes it relatively easy to analyze. 

Second, unlike nuclear DNA, which we inherit in a jumbled, mixed-up form from both our parents, mitochondrial DNA is passed on through the mother’s line only. Apparently, either the sperm cell does not contain mitochondria, or it is somehow excluded when the sperm enters the egg. So, when the fertilized cell divides, each new cell will contain copies of the egg’s mitochondria. Even if we look the “spitting image” of our father, every cell in our bodies is supposed to contain our mother’s mitochondrial DNA.

In trying to draw up the human family tree, therefore, researchers have taken a special interest in these minute strands of genetic code. What they are really interested in, however, is the variations in mitochondrial DNA from one group of people to another.

The Daughters are Tested

Although our mitochondrial DNA is probably the same as our mother’s mitochondrial DNA, small changes or mutations in the genetic code can arise. On rare occasions, mutations are serious enough to do harm. More often, however, the mutations have no effect on the proper functioning of the DNA or the mitochondria. In these cases, the changes will be preserved, and carried on through the female line to succeeding generations.

If we look further and further into the past, we will find that the number of women who contributed the modern varieties of mitochondrial DNA get less and less until, finally, we get to one “lucky” mother. She would be the only woman out of all the women living in her day to have a daughter in every generation till the present. Coming forward in time, we would see that the mitochondrial DNA varieties of her female contemporaries were gradually eliminated as their daughters did not have children, had only sons, or had daughters who did not have daughters. This doesn’t mean to say that we look like this ancestral mother, only that we all get our mitochondrial DNA from her.

To find this woman, researchers compared the different varieties of mitochondrial DNA in the human family. As mitochondrial DNA occurs in small quantities, and the researchers wanted a large sample from each person, they decided to use human placentas. So, Rebecca Cann and her colleagues selected 145 pregnant women and two cell lines representing the five major geographic regions: 20 Africans, 34 Asians, 46 Caucasians, 21 aboriginal Australians, and 26 aboriginal New Guineans (1987, p. 32). All placentas from the first three groups came from babies born in American hospitals. Only two of the 20 Africans were born in Africa.

The Tree of EveAfter analyzing a portion of the mitochondrial DNA in the cells of each placenta, they found that the differences grouped the samples by region. In other words, Asians were more like each other than they were like Europeans, New Guineans more like each other than they were like Australians, and so on.

Next, they saw two major branches in their computer-concocted tree of recent human evolution. Seven African individuals form one distinct branch that starts lower on the trunk than the other four. This is because the differences among these individuals are much greater than the differences between other individuals and other groups. More differences mean more mutations, and hence more time to accumulate those changes. If the Africans have more differences, then their lineage must be older than all the others. The second major branch bears the non-African groups and, significantly, a scattering of the remaining thirteen Africans in the sample. To the researchers, the presence of Africans among non-Africans meant an African common ancestor for the non-African branches which, likewise, meant an African common ancestor for both branches. The nickname “Eve” stuck to this hypothetical common ancestral mother, and later fired the media’s imagination.

“Eve’s” Birthday

Having concluded that the African group was the oldest, Cann and her colleagues wanted to find out how old. To do this, they used what is known as a molecular clock based, in this case, on mutations in mitochondrial DNA. The rate at which the clock is ticking is determined from the accumulation of changes over a given period of time. So, if two groups had a common ancestor 100,000 years ago, and if there is 0.2% difference in their genetic code, and if the rate of mutation is constant, then the rate of change is 0.2% per 100,000 years (or 2% every million years).

The researchers looked in two places for their figures. First, they compared mitochondrial DNA from humans with chimpanzees, and used paleontology and other molecular clock data to determine the age of the common ancestor. This, and similar calculations on other species, revealed a mutation rate in the range 2% to 4% per million years. Second, they compared groups in their study that were close geographically and took the age of the common ancestor from estimated times of settlement as indicated by anthropology and archaeology. Again, 2% to 4% every million years seemed reasonable to them.

As the common mitochondrial ancestor diverged from all others by 0.57%, she lived sometime between approximately 140,000 (0.57 ÷ 4 × 1,000,000) and 290,000 (0.57 ÷ 2 × 1,000,000) years ago. The figure of 200,000 was chosen as a suitable round number.

Theories Offered

The results obtained from analysis of mitochondrial DNA led to the “Out of Africa” theory. It is the idea that the descendants of mitochondrial “Eve” were the only ones to colonize Africa and the rest of the world, supplanting all other hominid populations in the process. If the descendants of Homo erectus groups living in China had mixed with their African counterparts, for example, then a distinct Asian branch would emerge on the tree. However, no other groups show as much variety as the African mitochondrial DNA pool. Further, if non-African females did not contribute any mitochondrial DNA, then it is possible that non-African populations did not contribute any nuclear DNA either. Evolutionists claim that such an interpretation is in accord with archaeologic, paleontologic, and other genetic data (Stringer and Andrews, 1988).

While many have accepted the mitochondrial DNA tree, they differ on the source of nuclear DNA and the humanity of “Eve.” Some believe she contributed all the nuclear DNA in addition to the mitochondrial DNA. Some believe she was an “archaic” Homo sapiens, while others believe she was fully human. The exact interpretation is debated because mitochondrial DNA is “something of a passenger in the genetic processes that lead to the formation of new species: it therefore neither contributes to the formation of a new species nor reveals anything about what actually happened” (Lewin, 1987, p. 24).

PROBLEMS WITH MITOCHONDRIAL “EVE”

Rebecca Cann and her colleagues obtained 145 placentas, extracted the mitochondrial DNA, analyzed certain portions of the genetic code, and used a computer program to derive the simplest or most parsimonious solution. All this work was carried out with assumptions, many of which are open to criticism on a scientific basis. Most important, their mitochondrial “Eve” is totally different from the biblical Eve; it is impossible to reconcile the two.

(1) Perhaps the most obvious problem relates to the molecular clock used to date the branches of “Eve’s” “family tree” and the appearance of “Eve” herself. Even those involved in the research are uncertain about the assumption of rate constancy. In addition, the “calibrations” of the clock are based on archaeology and paleontology, and involve a reliance on radiometric dating methods, evolutionary interpretations of the fossil record, and evolutionary views of cultural and social development.

(2) Evolutionists place “Eve” in a sequence of developing creatures. Depending on the model used, her ancestors may have been fully human, or an “archaic sapiens species” derived from an African population of Homo erectus. However, the true biblical Eve was the first woman; there were no preceding human or “sub-human” species. Adam called his wife Eve, because she was the mother of all the living (Genesis 3:20). Further, modern humanity owes its characteristics to the three sons of Noah and their wives; the genetic information of all others perished in the Flood. Thus, the most recent common mitochondrial forebear of all people living today would be the common female ancestor of Noah’s three daughters-in-law (this woman may have been Eve herself).

(3) Some objections surround the selection of contributors to the mitochondrial DNA sample. As many of the samples came from representatives of ethnic groups living in the U.S., there is a chance that the mitochondrial DNA may have been modified by intermarriages with other groups on the American continent. This limitation was supposedly overcome by excluding any pregnant woman whose family history involved cross-cultural mixing. Cann considered this screening process successful because most of the black Americans shared many mitochondrial DNA attributes with the African-born individuals. However, the possibility of genetic mixing is not eliminated altogether, in which case the results may change with a different sample set. This was the case for researchers at Emory University in Atlanta who, in conducting mitochondrial DNA research, took samples from 700 people on four continents. They also concluded that mitochondrial “Eve” originated around 200,000 years ago, but they suggested the place may have been Asia, rather than Africa. It should be noted that the biblical Eve originated not in Africa or Asia, but in the Garden of Eden—a place no longer in existence owing to the destructive force of the Noachian flood (Bromling, 1989).

(4) As with nuclear DNA, there are questions concerning both the theory and the actual mechanics of the experimental process. For example, is the process of accumulating mutations understood sufficiently? Does the technique assess an adequate proportion of codes along the mitochondrial DNA? Can mitochondrial DNA comparisons be used to indicate family relationships over long periods of time, or are there other complicating factors which would limit such use? These issues arise frequently in the scientific literature, although they are often dismissed as temporary gaps in knowledge. However, research is proceeding as if these answers will do nothing but vindicate the latest findings. Evolutionists derive some solace from their interpretation of the fossil record, which is used to confirm the assumptions and conclusions used in theories of molecular evolution. Such circular reasoning severely limits an unbiased consideration of the data.

(5) Lastly, other scientists find the popular “Out of Africa” interpretation unrealistic. Is it reasonable to expect a population to spread out over the whole world without ever interbreeding with other people? According to Milford Wolpoff of the University of Michigan, “In recorded history, there has always been intermixing as populations moved or villages exchanged wives. I believe we have a long history of people constantly mixing with one another and cooperating with one another and evolving into one great family” (quoted by Tierney, 1988, p. 51). Thus, if the interpretation requires special pleading (i.e., that no interbreeding occurred), then this may throw doubt on the method itself.

CONCLUSION

Who is this “Eve”? She is a hypothetical creature living tens of thousands of years ago; she allegedly lies somewhere in the evolutionary line of descent from Homo erectus to Homo sapiens; and she is the supposed source of all the varieties of mitochondrial DNA found in the world today. But she is not the Eve of Scripture; she is not the first female to be made in the image of God; she is not the woman created especially for Adam; and she is not the mother who bore Cain and Abel. The mitochondrial “Eve” issue is a good example of how the media can sensationalize a highly tenuous theory. To them, references to Eve and the Garden provide that additional twist to capture the public’s imagination, its attention, and thus its money. Upon further examination, calling this common ancestor “Eve” turns out to be a slap in the face of those people who respect the Word of God. Rather, ample valid scientific evidence exists to show the truth of human origins without having to embrace speculative and unscriptural ideas.

REFERENCES

Avise, John C. (1989), “Nature’s Family Archives,” Natural History, pp. 24-26, March.

Bromling, Brad T. (1989), “Will Eden Ever Be Found?,” The Restorer, 9[2]:6-7, February.

Cann, Rebecca L., Mark Stoneking, and Allan C. Wilson (1987), “Mitochondrial DNA and Human Evolution,” Nature, 325:31-36, January 1.

Denton, Michael (1985), Evolution: A Theory in Crisis (Bethesda, MD: Adler and Adler).

Edey, Maitland A. and Donald C. Johanson (1989), Blueprints (Boston: Little, Brown).

Gibson, L.J. (1987), “Do DNA Distances Reveal Avian Phylogeny?,” Origins (Loma Linda, CA: Geoscience Research Institute), 14[2]:47-76.

Kirsch, John A.W. and Carey Krajewski (1988), “Letters: Conflict Over the Molecular Clock,” Science, 242:1624, December 23.

Lemonick, Michael D. (1987), “Everyone’s Genealogical Mother,” Time, p. 66, January 26.

Lewin, Roger (1987), “The Unmasking of Mitochondrial Eve,” Science, 238:24-26, October 2.

Lewin, Roger (1988a), “Conflict Over DNA Clock Results,” Science, 241:1598-1600, September 23.

Lewin, Roger (1988b), “DNA Clock Conflict Continues,” Science, 241:1756-1759, September 30.

Major, Trevor and Bert Thompson (1986), “Evolution, Creation, and the Fossil Record—[Parts I-III]” Reason & Revelation, 6:27-38, July/August/September.

Stringer, C.B. and P. Andrews (1988), “Genetic and Fossil Evidence for the Origin of Modern Humans,” Science, 239:1263-1268, March 11.

Tierney, John, Lynda Wright, and Karen Springen (1988), “The Search for Adam and Eve,” Newsweek, pp. 46-52, January 11.

AUTHOR’S POSTSCRIPT, 1992

Research that purports to confirm Cann’s findings has appeared in the years since my article was published (e.g., Vigilant, et al., 1991). Meanwhile, Milford Wolpoff and others have continued to pit their fossils against the molecular data (see the debate in the April 1992 issue of Scientific American). More important, various geneticists have criticized the statistical basis of the “Eve” hypothesis. They have shown that other trees with non-African roots are possible, but that the variation among these computer-generated solutions is so great as to negate any conclusions about human evolution that might be based on mitochondrial DNA (e.g., Templeton, et al., 1992).

Templeton, A.R., S.B. Hedges, S. Kumar, and K. Tamura (1992), “Human Origins and Analysis of Mitochondrial DNA Sequences,” Science, 255:737-739, February 2.

Vigilant, Linda, et al. (1991), “African Populations and the Evolution of Human Mitochondrial DNA,” Science, 253:1503-1507, September 27.


Originally published in Reason & Revelation, April 1989, 9[4]:13-16. Copyright © 1989 Apologetics Press, Inc. All rights reserved.


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Wednesday, September 28, 2022

Origins and the "Created Kind" Concept

 

Origins and the "Created Kind" Concept

Q.

The Bible speaks of things reproducing “after their kind.” What does the biblical word “kind” indicate?

A.

Today, most creationists take the view that variation and speciation can occur only within created kinds. These kinds appeared for the first time in the creation week and have since colonized the Earth. For land-dwelling animals, modern representatives would have to be the descendants of the kinds carried on the ark (Genesis 6:17; 8:17-19).

However, there is no consensus on the biological definition of kind, or the criteria for grouping animals within a kind. Some creationists equate the term with a particular taxonomic level higher than species, such as genus or family. Most, however, avoid such comparisons altogether. Byron Nelson wrote:

The “kinds” of Genesis refer not to the “systematic” species identified by men, but to those natural species of which the world is full, which have power to vary within themselves in such a way that the members of the species are not all exactly alike, but which, nevertheless, cannot go out of the bounds that the creator set (1967, p. 4).

In 1941, Frank Marsh coined the term “baramin”—a compound of the Hebrew word's bara (“created”) and min (“kind”). He suggested that the nearest equivalent to the created kind would vary, depending on the greatest taxonomic level at which two organisms could interbreed (1976, p. 34). For example, while there are several species of cattle and bison, they probably belong to the same kind because they all can interbreed (Marsh, 1976, p. 31).

The differences of opinion, and the apparent flexibility in the idea, have given Anti creationists cause for criticism. Joel Cracraft complained:

The “created kind” is the unit of creation event just as the species is the unit of evolutionary change. Consequently, if the concept of “created kind” cannot be defined so that it can be used to interpret and investigate nature, then it is of little or no importance for the growth of knowledge (1983, p. 169).

However, the same sort of criticisms leveled at kinds also can be turned on the species concept, which is neither well defined nor objective. First, the widely held biological species concept “holds that a species is a population of organisms that can at least potentially breed with one another but that do not breed with other populations” (Rennie, 1991). Unfortunately, two populations may not breed because they are isolated geographically. This may lead to taxonomic splitting, by which taxonomists give two different names to populations that could interbreed if given the chance. Practically speaking, very few species undergo extensive cross-breeding experiments before classification to test their reproductive isolation. Hybridization is another problem. Two seemingly distinct plant species may cross to produce fertile hybrids.

The potential for taxonomic splitting is especially acute in the fossil record, where it is impossible to apply the biological species concept. Instead, paleontologists tend to define species on their morphology alone. However, the soft parts of an organism rarely are preserved, and the identification must rest almost entirely on hard parts (e.g., bones, teeth, etc.). Any evolutionary relationships drawn from such studies are necessarily limited (Major, 1991).

Second, the species idea often takes on a definite evolutionary connotation. As we have already seen, Cracraft claims that the species is “the unit of evolutionary change” (1983, p. 169). He wants to replace the biological species concept with his own phylogenetic species concept, mainly because he is not satisfied with any definition that ignores alleged evolutionary relationships. Cracraft’s concept defines a species as “the smallest recognizable cluster of individuals that share a common pattern of ancestry” (Rennie, 1991).

The created kind concept can hold its own against these definitions. It proposes that a kind will consist of populations that can interbreed, while still allowing room for variation. If implemented systematically, the concept would reveal barriers or discontinuities between created kinds. “In order to make this evidence of creation available,” Kurt Wise has suggested, “there is a serious need for creation biologists to create, adopt, and employ a reproducible method of flagging identifiable phyletic discontinuities” (1990, 2:354). Creationists, like Wise, are continuing their work on kinds. In the meantime, we face a taxonomic system encumbered with evolutionary presuppositions.

REFERENCES

Cracraft, Joel (1983), “Systematics, Comparative Biology, and the Case against Creationism,” Scientists Confront Creationism, ed. Laurie R. Godfrey (New York: W.W. Norton), pp. 163-191.

Major, Trevor (1991), “Problems in the Interpretation of Variation Within the Fossil Record,” Creation Research Society Quarterly, 28:52-53, September.

Marsh, Frank L. (1976), Variation and Fixity in Nature (Mountain View, CA: Pacific Press).

Nelson, Byron (1967), After Its Kind (Minneapolis, MN: Bethany Fellowship).

Rennie, John (1991), “Are Species Specious?,” Scientific American, 265[5]:26, November.

Wise, Kurt P. (1990), “Baraminology: A Young-Earth Creation Biosystematic Method,” Proceedings of the Second International Conference on Creationism, July 30-August 4, 1990, ed. Robert E. Walsh (Pittsburgh, PA: Creation Science Fellowship), pp. 345-360.


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Tuesday, September 27, 2022

From Nonlife to Nonlife

 

From Nonlife to Nonlife

Q.

Organic evolution is based on the concept of something inorganic and nonliving becoming organic and living. Do the actual scientific data support such a concept?

A.

How did life arise from nonliving chemicals? This is the most fundamental, yet sketchiest chapter of evolutionary theory.

One proposal is to start with seemingly lifelike chemicals. This is the approach taken by Julius Rebek and his coworkers (Hong, et al., 1992; Feng, et al., 1992). Like DNA, Rebek’s chemicals can make copies of themselves (i.e., replicate). Further, Rebek can make more efficient replicators by subjecting them to ultraviolet radiation. These new varieties outproduce other forms, eventually dominating their test-tube world. Supposedly, these chemicals could provide the missing link between nonlife and life.

Yet, the gap remains because Rebek’s system contains little information (see Hurst and Dawkins, 1992, 357:199). Life is defined by a set of elegant instructions recorded on the DNA molecule, and there is more to life than replication.

Another proposal tries to circumvent the famous chicken-and-egg problem of chemical evolution by starting with RNA. If we think of DNA as the “brain,” then RNA is the “nervous system” carrying the message of protein formation to the rest of the cell. However, the whole process involves crucial enzymes (specialized proteins). So, which came first, the protein or the DNA?

The answer, many evolutionists believe, lies in the discovery that a special part of RNA can act like an enzyme. This means it can carry information and do various jobs within the cell. If this is the case, then perhaps evolution worked both ways, turning RNA into DNA for better information storage, and into specialized enzymes for more efficient copying. Last year, the proponents of this RNA world received a boost from the work of Beaudry and Joyce (1992) who used selection and mutations to make a more efficient RNA enzyme.

Some journalists and scientists have made extraordinary claims about this new research. First, they described the techniques and chemical processes in evolutionary terms such as “selection” and “mutation.” One newspaper article hailed Beaudry and Joyce’s work as the “first complete laboratory demonstration of evolution” (Graham, 1992). Second, they believe the experiments show that “Darwinian selection is universal for all lifes” (Hurst and Dawkins, 1992, 357:198), not just for “life as we know it.” And third, because this research has a practical application in biotechnology, they wish to promote evolution as a fundamental tool of science, and not a mere theory.

However, using terms such as selection, mutation, and evolution does not explain the origin of life. These experiments entail a great deal of design and technical innovation. The human experimenters are forcing or directing “evolution” to achieve goals they have set (Culotta, 1992). As Leslie Orgel noted, to really show how life could have evolved, we need to start with something that does not require the “intervention of organic chemists” (1992, 358:207).

Further, this research may come closer to Darwin’s arguments than they would really like. By showing that man can use artificial selection to change species dramatically, even within recorded history, Darwin hoped to establish his case for long-term, large-scale evolution by natural selection (1859, pp. 133,153). But this analogy breaks down because artificial selection, by definition, involves human intelligence. The same is true for this recent research. We are seeing nothing more than high-tech horse breeding. Actually, we may be seeing less, because the experiments do not deal with life at all. If anything, they resemble Edison’s efforts to find a better filament for his electric light bulb.

What we must emphasize is that an evolutionist can invent any theory about the origin of life, no matter how implausible it may sound. He might succeed in modeling that theory in the laboratory. However, a model is not necessarily the same as reality; he has not proved that life evolved in that way. Ultimately, all he would have displayed is his God-given intellectual and physical abilities.

REFERENCES

Beaudry, Amber A. and Gerald F. Joyce (1992), “Directed Evolution of an RNA Enzyme,” Science, 257:635-641, July 31.

Culotta, Elizabeth (1992), “Forcing the Evolution of an RNA Enzyme in the Test Tube,” Science, 257:613, July 31.

Darwin, Charles (1859), The Origin of Species (New York: Avenel Books, 1979 reprint of the 1968 Penguin edition).

Feng, Qing, Tae Kyo Park and Julius Rebek, Jr. (1992), “Crossover Reactions Between Synthetic Replicators Yield Active and Inactive Recombinants,” Science, 256:1179-1180, May 22.

Graham, David (1992), “Evolution in the Lab at Scripps,” San Diego-Union Tribune, July 31, pp. A1-A2, July 31.

Hong, Jong-In, Qing Feng, Vincent Rotello and Julius Rebek, Jr. (1992), “Competition, Cooperation, and Mutation: Improving a Synthetic Replicator by Light Irradiation,” Science, 255:848-850, February 14.

Hurst, Lawrence D. and Richard Dawkins (1992), “Life in a Test Tube,” Nature, 357:198-199, May 21.

 



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Monday, September 26, 2022

Was the Behemoth of Job 40:15 a Dinosaur?

 

Was the Behemoth of Job 40:15 a Dinosaur?

 

Q.

Some writers have suggested that “behemoth,” mentioned in Job 40:15ff., could have been a type of dinosaur. However, since the Bible mentions behemoth’s “navel” (40:16), would not this exclude dinosaurs, since they were egg-layers and would not have possessed navels?

 

A.

The word rendered “navel” in the King James Version of the Bible derives from the Hebrew term sharir. Scholars have suggested that the term originally meant “firm, hard,” hence, denoted “the firm parts of the belly” (Gesenius, 1979, p. 850). In Job 40:16, it thus means “sinew, muscle” (see Brown, et al., 1906, p. 1057; Harris, et al., 1980, 2:957).

In Job 40:16, the term is the plural form. Would anyone suggest that the behemoth had more than one navel? The comments of Albert Barnes are appropriate:

The word here rendered navel means properly firm, hard, tough, and in the plural form, which occurs here, means the firm, or tough parts of the belly. It is not used to denote the navel in any place in the Bible, and should not have been rendered so here (1949, 2:248).

While many commentators have identified behemoth with the elephant or the hippopotamus, elsewhere I have argued that the descriptions given in the book of Job do not fit either of these animals (see Jackson, 1983, pp. 86-87) and that there is no valid reason for rejecting the idea that behemoth could have been some species of dinosaur.

Those who reject this possibility do so solely on the assumption that dinosaurs and man were never contemporary—a view that not only is contrary to principles of sound biblical interpretation, but is, in fact, saturated with evolutionary presuppositions. Were it not for modern-day influences of evolutionary pseudoscience, certain Bible believers would have no problem at all with such passages as this.

 

REFERENCES

 

Barnes, Albert (1949 reprint), Notes on the Old and New Testaments—Job (Grand Rapids, MI: Baker).

Brown, F., S. Driver, and C. Briggs (1906) Hebrew and English Lexicon (Boston, MA: Houghton-Mifflin).

Gesenius, William (1979 reprint), Hebrew-Chaldee Lexicon of the Old Testament (Grand Rapids, MI: Baker).

Harris, R.L., G.L. Archer, and B.K. Waltke (1980), Theological Wordbook of the Old Testament (Chicago, IL: Moody).

Jackson, Wayne (1983), The Book of Job—Analyzed and Applied (Abilene, TX: Quality).

 


Originally published in Reason and Revelation, December 1986, 6[12]:47. Copyright © 1986 Apologetics Press, Inc. All Rights Reserved.

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