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. Anti-evolutionists 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.
Strength and Acceptance of the Theory
Seen in the light of evolution, biology is, perhaps, intellectually the most satisfying and inspiring science. Without that light it becomes a pile of sundry facts some of them interesting or curious but making no meaningful picture as a whole.
This is not to imply that we know everything that can and should be known about biology and about evolution. Any competent biologist is aware of a multitude of problems yet unresolved and of questions yet unanswered. After all, biologic research shows no sign of approaching completion; quite the opposite is true. Disagreements and clashes of opinion are rife among biologists, as they should be in a living and growing science. Anti-evolutionists mistake, or pretend to mistake, these disagreements as indications of dubiousness of the entire doctrine of evolution. Their favorite sport is stringing together quotations, carefully and sometimes expertly taken out of context, to show that nothing is really established or agreed upon among evolutionists. Some of my colleagues and myself have been amused and amazed to read ourselves quoted in a way showing that we are really anti-evolutionists under the skin.