Evolusi

[E = mc²]

Unity of Life

The unity of life is no less remarkable than its diversity. Most forms of life are similar in many respects. The universal biologic similarities are particularly striking in the biochemical dimension. From viruses to man, heredity is coded in just two, chemically related substances: DNA and RNA. The genetic code is as simple as it is universal. There are only four genetic "letters" in DNA: adenine, guanine, thymine, and cytosine. Uracil replaces thymine in RNA. The entire evolutionary development of the living world has taken place not by invention of new "letters" in the genetic "alphabet" but by elaboration of ever-new combinations of these letters.

Not only is the DNA-RNA genetic code universal, but so is the method of translation of the sequences of the "letters" in DNA-RNA into sequences of amino acids in proteins. The same 20 amino acids compose countless different proteins in all, or at least in most, organisms. Different amino acids are coded by one to six nucleotide triplets in DNA and RNA. And the biochemical universals extend beyond the genetic code and its translation into proteins: striking uniformities prevail in the cellular metabolism of the most dirverse living beings. Adenosine triphosphate, biotin, riboflavin, hemes, pyridoxin, vitamins K and B12, and folic acid implement metabolic processes everywhere.

What do these biochemical or biologic universals mean? They suggest that life arose from inanimate matter only once and that all organisms, no matter now diverse, in other respects, conserve the basic features of the primordial life. (It is also possible that there were several, or even many, origins of life; if so, the progeny of only one of them has survived and inherited the earth.) But what if there was no evolution and every one of the millions of species were created by separate fiat? However offensive the notion may be to religious feeling and to reason, the antievolutionists must again accuse the Creator of cheating. They must insist that He deliberately arranged things exactly as if his method of creation was evolution, intentionally to mislead sincere seekers of truth.

The remarkable advances of molecular biology in recent years have made it possible to understand how it is that diverse organisms are constructed from such monotonously similar materials: proteins composed of only 20 kinds of amino acids and coded only by DNA and RNA, each with only four kinds of nucleotides. The method is astonishingly simple. All English words, sentences, chapters, and books are made up of sequences of 26 letters of the alphabet. (They can be represented also by only three signs of the Morse code: dot, dash, and gap.) The meaning of a word or a sentence is defined not so much by what letters it contains as by the sequences of these letters. It is the same with heredity: it is coded by the sequences of the genetic "letters" the nucleotides in the DNA. They are translated into the sequences of amino acids in the proteins.

Molecular studies have made possible an approach to exact measurements of degrees of biochemical similarities and differences among organisms. Some kinds of enzymes and other proteins are quasiuniversal, or at any rate widespread, in the living world. They are functionally similar in different living beings, in that they catalyze similar chemical reactions. But when such proteins are isolated and their structures determined chemically, they are often found to contain more or less different sequences of amino acids in different organisms. For example, the so-called alpha chains of hemoglobin have identical sequences of amino acids in man and the chimpanzee, but they differ in a single amino acid (out of 141) in the gorilla. Alpha chains of human hemoglobin differ from cattle hemoglobin in 17 amino acid substitutions, 18 from horse, 20 from donkey, 25 from rabbit, and 71 from fish (carp).

Cytochrome C is an enzyme that plays an important role in the metabolism of aerobic cells. It is found in the most diverse organisms, from man to molds. E. Margoliash, W. M. Fitch, and others have compared the amino acid sequences in cytochrome C in different branches of the living world. Most significant similarities as well as differences have been brought to light. The cytochrome C of different orders of mammals and birds differ in 2 to 17 amino acids, classes of vertebrates in 7 to 38, and vertebrates and insects in 23 to 41; and animals differ from yeasts and molds in 56 to 72 amino acids. Fitch and Margoliash prefer to express their findings in what are called "minimal mutational distances." It has been mentioned above that different amino acids are coded by different triplets of nucleotides in DNA of the genes; this code is now known. Most mutations involve substitutions of single nucleotides somewhere in the DNA chain coding for a given protein. Therefore, one can calculate the minimum numbers of single mutations needed to change the cytochrome C of one organism into that of another. Minimal mutational distances between human cytochrome C and the cytochrome C of other living beings are as follows:

monkey	1	chicken	18
dog	13	penguin	18
horse	17	turtle	19
donkey	16	rattlesnake	20
pig	13	fish (tuna)	31
rabbit	12	fly	33
kangaroo	12	moth	36
duck	17	mold	63
pigeon	16	yeast	56

It is important to note that amino acid sequences in a given kind of protein vary within a species as well as from species to species. It is evident that the differences among proteins at the level of species, genus, family, order, class, and phylum are compounded of elements that vary also among individuals within a species. Individual and group differences are only quantitatively, not qualitatively, different. Evidence supporting the above propositions is ample and is growing rapidly. Much work has been done in recent years on individual variations in amino acid sequences of hemoglobin of human blood. More that 100 variants have been detected. Most of them involve substitutions of single amino acids – substitutions that have arisen by genetic mutations in the persons in whom they are discovered or in their ancestors. As expected, some of these mutations are deleterious to their carriers, but others apparently are neutral or even favorable in certain environments. Some mutant hemoglobins have been found only in one person or in one family; others are discovered repeatedly among inhabitants of different parts of the world. I submit that all these remarkable findings make sense in the light of evolution: they are nonsense otherwise.

Comparative Anatomy and Embryology

The biochemical universals are the most impressive and the most recently discovered, but certainly they are not the only vestiges of creation by means of evolution. Comparative anatomy and embryology proclaim the evolutionary origins of the present inhabitants of the world. In 1555 Pierre Belon established the presence of homologous bones in the superficially very different skeletons of man and bird. Later anatomists traced the homologies in the skeletons, as well as in other organs, of all vertebrates. Homologies are also traceable in the external skeletons of arthropods as seemingly unlike as a lobster, a fly, and a butterfly. Examples of homologies can be multiplied indefinitely.

Embryos of apparently quite diverse animals often exhibit striking similarities. A century ago these similarities led some biologists (notably the German zoologist Ernst Haeckel) to be carried by their enthusiasm as far as to interpret the embryonic similarities as meaning that the embryo repeats in its development the evolutionary history of its species: it was said to pass through stages in which it resembles its remote ancestors. In other words, early-day biologists supposed that by studying embryonic development one can, as it were, read off the stages through which the evolutionary development had passed. This so-called biogenetic law is no longer credited in its original form. And yet embryonic similarities are undeniable impressive and significant.

Probably everybody knows the sedentary barnacles which seem to have no similarity to free-swimming crustaceans, such as the copepods. How remarkable that barnacles pass through a free-swimming larval stage, the nauplius! At that stage of its development a barnacle and a Cyclops look unmistakably similar. They are evidently relatives. The presence of gill slits in human embryos and in embryos of other terrestrial vertebrates is another famous example. Of course, at no stage of its development is a human embryo a fish, nor does it ever have functioning gills. But why should it have unmistakable gill slits unless its remote ancestors did respire with the aid of gills? It is the Creator again playing practical jokes?

Adaptive radiation: Hawaii’s Flies

There are about 2,000 species of drosophilid flies in the world as a whole. About a quarter of them occur in Hawaii, although the total area of the archipelago is only about that of the state of New Jersey. All but 17 of the species in Hawaii are endemic (found nowhere else). Furthermore, a great majority of the Hawaiian endemics do not occur throughout the archipelago: they are restricted to single islands or even to a part of an island. What is the explanation of this extraordinary proliferation of drosophilid species in so small a territory? Recent work of H. L. Carson, H. T. Spieth, D. E. Hardy, and others makes the situation understandable.

The Hawaiian Islands are of volcanic origin; they were never parts of any continent. Their ages are between 5.6 and 0.7 million years. Before man came there inhabitants were descendants of immigrants that had been transported across the ocean by air currents and other accidental means. A single drosophilid species, which arrived in Hawaii first, before there were numerous competitors, faced the challenge of an abundance of many unoccupied ecologic niches. Its descendants responded to this challenge by evolutionary adaptive radiation, the products of which are the remarkable Hawaiian drosophilids of today. To forestall a possible misunderstanding, let it be made clear that the Hawaiian endemics are by no means so similar to each other that they could be mistaken for variants of the same species; if anything, they are more diversified than are drosophilids elsewhere. The largest and the smallest drosophilid species are both Hawaiian. They exhibit an astonishing variety of behavior patterns. Some of them have become adapted to ways of life quite extraordinary for a drosophilid fly, such as being parasites in egg cocoons of spiders.

Oceanic islands other than Hawaii, scattered over the wide Pacific Ocean, are not conspicuously rich in endemic species of drosophilids. The most probable explanation of this fact is that these other islands were colonized by drosophilid after most ecologic niches had already been filled by earlier arrivals. This surely is a hypothesis, but it is a reasonable one. Antievolutionists might perhaps suggest an alternative hypothesis: in a fit of absentmindedness, the Creator went on manufacturing more and more drosophilid species for Hawaii, until there was an extravagant surfeit of them in this archipelago. I leave it up to you to decide which hypothesis makes sense.