Exclusive sib mating destroys the major premise of Fisher’s argument for one to one sex ratios. If females are always fertilized by their brothers, then the same parents manufacture both partners of any mating. Fisher assumed that the males had different parents and that an undersupply of males awarded genetic advantages to those parents that could produce males preferentially. But if the same parents produce both the mothers and fathers of their grandchildren, then they have an equal genetic investment in each grandchild, no matter what percentage of males and females they produce among their children. In this case, the reason for an equal balance of males and females disappears and the previous argument for female predominance reasserts itself. If each pair of grandparents has a limited store of energy to invest in offspring, and if grandparents producing more offspring gain a Darwinian edge, then grandparents should make as many daughters as possible, and produce only enough sons to ensure that all their daughters will be fertilized. In fact, if their sons can muster sufficient sexual prowess, then parents should make just one son and use every bit of remaining energy to produce as many daughters as they can. As usual, bountiful nature comes to our aid with numerous exceptions to probe Fisher’s rule: indeed, species with sib mating also tend to produce a minimal number of males.
Consider the curious life of a male mite in the genus Adactylidium, as described by E.A. Albadry and M.S.F. Tawfik in 1966. It emerges from its mother’s body and promptly dies within a few hours, having done apparently nothing during its brief life. It attempts, while outside its mother, neither to feed nor to mate. We know about creatures with short adult lives—the mayfly’s single day after a much lengthier larval life, for example. But the mayfly mates and insures the continuity of its kind during these few precious hours. The males of Adactylidium seem to do nothing at all but emerge and die.
To solve the mystery, we must study the entire life cycle and look inside the mother’s body. The impregnated female of Adactylidium attaches to the egg of a thrips. That single egg provides the only source of nutrition for rearing all her offspring—for she will feed on nothing else before her death. This mite, so far as we know, engages exclusively in sib mating; thus, it should produce a minimal number of males. Moreover, since total reproductive energy is so strongly constrained by the nutritional resources of a single thrips’ egg, progeny are strictly limited, and the more females the better. Indeed, Adactylidium matches our prediction by raising a brood of five to eight sisters accompanied by a single male who will serve as both brother and husband to them all. But producing a single male is chancy; if it dies, all sisters will remain virgins and their mother’s evolutionary life is over.
If the mite takes a chance on producing but a single male, thus maximizing its potential brood of fertile females, two other adaptations might lessen the risk—providing both protection for the male and guaranteed proximity to his sisters. What better than to rear the brood entirely within a mother’s body, feeding both larvae and adults within her, and even allowing copulation to occur inside her protective shell. Indeed, about forty-eight hours after she attaches to the thrips’ egg, six to nine eggs hatch within the body of a female Adactylidium. The larvae feed on their mother’s body, literally devouring her from inside. Two days later, the offspring reach maturity, and the single male copulates with all his sisters. By this time, the mother’s tissues have disintegrated, and her body space is a mass of adult mites, their feces, and their discarded larval and nymphal skeletons. The offspring then cut holes through their mother’s body wall and emerge. The females must now find a thrips’ egg and begin the process again, but the males have already fulfilled their evolutionary role before “birth.” They emerge, react however a mite does to the glories of the outside world, and promptly die.
But why not carry the process one stage further? Why should the male be born at all? After copulating with its sisters, its work is done. It is ready to chant the acarine version of Simeon’s prayer, Nunc dimittis—Oh Lord, now lettest thou thy servant depart in peace. Indeed, since everything that is possible tends to occur at least once in the multifarious world of life, a close relative of Adactylidium does just this. Acarophenax tribolii also indulges exclusively in sib mating. Fifteen eggs, including but a single male, develop within the mother’s body. The male emerges within his mother’s shell, copulates with all his sisters and dies before birth. It may not sound like much of a life, but the male Acarophenax does as much for its evolutionary continuity as Abraham did in fathering children into his tenth decade.
Nature’s oddities are more than good stories. They are material for probing the limits of interesting theories about life’s history and meaning.
7 | Shades of Lamarck
THE WORLD, UNFORTUNATELY, rarely matches our hopes and consistently refuses to behave in a reasonable manner. The psalmist did not distinguish himself as an acute observer when he wrote: “I have been young, and now am old; yet have I not seen the righteous forsaken, nor his seed begging bread.” The tyranny of what seems reasonable often impedes science. Who before Einstein would have believed that the mass and aging of an object could be affected by its velocity near the speed of light?
Since the living world is a product of evolution, why not suppose that it arose in the simplest and most direct way? Why not argue that organisms improve themselves by their own efforts and pass these advantages to their offspring in the form of altered genes—a process that has long been called, in technical parlance, the “inheritance of acquired characters.” This idea appeals to common sense not only for its simplicity but perhaps even more for its happy implication that evolution travels an inherently progressive path, propelled by the hard work of organisms themselves. But, as we all must die, and as we do not inhabit the central body of a restricted universe, so the inheritance of acquired characters represents another human hope scorned by nature.
The inheritance of acquired characters usually goes by the shorter, although historically inaccurate, name of Lamarckism. Jean Baptiste Lamarck (1744–1829), the great French biologist and early evolutionist, believed in the inheritance of acquired characters, but it was not the centerpiece of his evolutionary theory and was certainly not original with him. Entire volumes have been written to trace its pre-Lamarckian pedigree (see Zirkle in bibliography). Lamarck argued that life is generated, continuously and spontaneously, in very simple form. It then climbs a ladder of complexity, motivated by a “force that tends incessantly to complicate organization.” This force operates through the creative response of organisms to “felt needs.” But life cannot be organized as a ladder because the upward path is often diverted by requirements of local environments; thus, giraffes acquire long necks and wading birds webbed feet, while moles and cave fishes lose their eyes. Inheritance of acquired characters does play an important part in this scheme, but not the central role. It is the mechanism for assuring that offspring benefit from their parents’ efforts, but it does not propel evolution up the ladder.
In the late nineteenth century, many evolutionists sought an alternative to Darwin’s theory of natural selection. They reread Lamarck, cast aside the guts of it (continuous generation and complicating forces), and elevated one aspect of the mechanics—inheritance of acquired characters—to a central focus it never had for Lamarck himself. Moreover, many of these self-styled “neo-Lamarckians” abandoned Lamarck’s cardinal idea that evolution is an active, creative response by organisms to their felt needs. They preserved the inheritance of acquired characters but viewed the acquisitions as direct impositions by impressing environments upon passive organisms.
Although I will bow to contemporary usage and define Lamarckism as the notion that organisms evolve by acquiring adaptive characters and passing them on to offspring in the form of altered genetic information, I do wish to record how poorly this name honors a very fine scientist who died 150 years ago. Subtlety and richness are so often degraded in our world. Consider the poor marshmallow—the plant, that is. Its roots once made a fine cand
y; now its name adheres to that miserable ersatz of sugar, gelatine, and corn syrup.
Lamarckism, in this sense, remained a popular evolutionary theory well into our century. Darwin won the battle for evolution as a fact, but his theory for its mechanism—natural selection—did not win wide popularity until the traditions of natural history and Mendelian genetics were fused during the 1930s. Moreover, Darwin himself did not deny Lamarckism, although he regarded it as subsidiary to natural selection as an evolutionary mechanism. As late as 1938, for example, Harvard paleontologist Percy Raymond, writing (I suspect) at the very desk I am now using, said of his colleagues: “Probably most are Lamarckians of some shade; to the uncharitable critic it might seem that many out-Lamarck Lamarck.” We must recognize the continuing influence of Lamarckism in order to understand much social theory of the recent past—ideas that become incomprehensible if forced into the Darwinian framework we often assume for them. When reformers spoke of the “taint” of poverty, alcoholism, or criminality, they usually thought in quite literal terms—the sins of the father would extend in hard heredity far beyond the third generation. When Lysenko began to advocate Lamarckian cures for the ills of Soviet agriculture during the 1930s, he had not resuscitated a bit of early nineteenth-century nonsense, but a still respectable, if fast fading, theory. Although this tidbit of historical information does not make his hegemony, or the methods he used to retain it, any less appalling, it does render the tale a bit less mysterious. Lysenko’s debate with the Russian Mendelians was, at the outset, a legitimate scientific argument. Later, he held on through fraud, deception, manipulation, and murder—that is the tragedy.
Darwin’s theory of natural selection is more complex than Lamarckism because it requires two separate processes, rather than a single force. Both theories are rooted in the concept of adaptation—(he idea that organisms respond to changing environments by evolving a form, function, or behavior better suited to these new circumstances. Thus, in both theories, information from the environment must be transmitted to organisms. In Lamarckism, the transfer is direct. An organism perceives the environmental change, responds in the “right” way, and passes its appropriate reaction directly to its offspring.
Darwinism, on the other hand, is a two-step process, with different forces responsible for variation and direction. Darwinians speak of genetic variation, the first step, as “random.” This is an unfortunate term because we do not mean random in the mathematical sense of equally likely in all directions. We simply mean that variation occurs with no preferred orientation in adaptive directions. If temperatures are dropping and a hairier coat would aid survival, genetic variation for greater hairiness does not begin to arise with increased frequency. Selection, the second step, works upon unoriented variation and changes a population by conferring greater reproductive success upon advantageous variants.
This is the essential difference between Lamarckism and Darwinism—for Lamarckism is, fundamentally, a theory of directed variation. If hairy coats are better, animals perceive the need, grow them, and pass the potential to offspring. Thus, variation is directed automatically toward adaptation and no second force like natural selection is needed. Many people do not understand the essential role of directed variation in Lamarckism. They often argue: isn’t Lamarckism true because environment does influence heredity—chemical and radioactive mutagens increase the mutation rate and enlarge a population’s pool of genetic variation. This mechanism increases the amount of variation but does not propel it in favored directions. Lamarckism holds that genetic variation originates preferentially in adaptive directions.
In the June 2, 1979, issue of Lancet, the leading British medical journal, for example, Dr. Paul E. M. Fine argues for what he calls “Lamarckism” by discussing a variety of biochemical paths for the inheritance of acquired, but non-directed, genetic variation. Viruses, essentially naked bits of DNA, may insert themselves into the genetic material of a bacterium and be passed along to offspring as part of the bacterial chromosome. An enzyme called “reverse transcriptase” can mediate the reading of information from cellular RNA “back” into nuclear DNA. The old idea of a single, irreversible flow of information from nuclear DNA through intermediary RNA to proteins that build the body does not hold in all cases—even though Watson himself had once sanctified it as the “central dogma” of molecular biology: DNA makes RNA makes protein. Since an inserted virus is an “acquired character” that can be passed along to offspring, Fine argues that Lamarckism holds in some cases. But Fine has misunderstood the Lamarckian requirement that characters be acquired for adaptive reasons—for Lamarckism is a theory of directed variation. I have heard no evidence that any of these biochemical mechanisms leads to the preferential incorporation of favorable genetic information. Perhaps this is possible; perhaps it even happens. If so, it would be an exciting new development, and truly Lamarckian.
But so far, we have found nothing in the workings of Mendelism or in the biochemistry of DNA to encourage a belief that environments or acquired adaptations can direct sex cells to mutate in specific directions. How could colder weather “tell” the chromosomes of a sperm or egg to produce mutations for longer hair? How could Pete Rose transfer hustle to his gametes? It would be nice. It would be simple. It would propel evolution at much faster rates than Darwinian processes allow. But it is not nature’s way, so far as we know.
Yet Lamarckism holds on, at least in popular imagination, and we must ask why? Arthur Koestler, in particular, has vigorously defended it in several books, including The Case of the Midwife Toad, a full-length attempt to vindicate the Austrian Lamarckian Paul Kammerer, who shot himself in 1926 (although largely for other reasons) after the discovery that his prize specimen had been doctored by an injection of India ink. Koestler hopes to establish at least a “mini-Lamarckianism” to prick the orthodoxy of what he views as a heartless and mechanistic Darwinism. I think that Lamarckism retains its appeal for two major reasons.
First, a few phenomena of evolution do appear, superficially, to suggest Lamarckian explanations. Usually, the Lamarckian appeal arises from a misconception of Darwinism. It is often and truly stated, for example, that many genetic adaptations must be preceded by a shift in behavior without genetic foundation. In a classic and recent case, several species of tits learned to pry the tops off English milk bottles and drink the cream within. One can well imagine a subsequent evolution of bill shape to make the pilferage easier (although it will probably by nipped in the bud by paper cartons and a cessation of home delivery). Is this not Lamarckian in the sense that an active, nongenetic behavioral innovation sets the stage for reinforcing evolution? Doesn’t Darwinism think of the environment as a refining fire and organisms as passive entities before it?
But Darwinism is not a mechanistic theory of environmental determinism. It does not view organisms as billiard balls, buffeted about by a shaping environment. These examples of behavioral innovation are thoroughly Darwinian—yet we praise Lamarck for emphasizing so strongly the active role of organisms as creators of their environment. The tits, in learning to invade milk bottles, established new selective pressures by altering their own environment. Bills of a different shape will now be favored by natural selection. The new environment does not provoke the tits to manufacture genetic variation directed toward the favored shape. This, and only this, would be Lamarckian.
Another phenomenon, passing under a variety of names, including the “Baldwin effect” and “genetic assimilation,” seems more Lamarckian in character but fits just as well into a Darwinian perspective. To choose the classic illustration: Ostriches have callosities on their legs where they often kneel on hard ground; but the callosities develop within the egg, before they can be used. Does this not require a Lamarckian scenario: Ancestors with smooth legs began to kneel and acquire callosities as a nongenetic adaptation, just as we, depending on our profession, develop writer’s calluses or thickened soles. These callosities were then inherited as genetic adaptations, forming w
ell before their use.
The Darwinian explanation for “genetic assimilation” can be illustrated with the midwife toad of Paul Kammerer, Koestler’s favorite example—for Kammerer, ironically, performed a Darwinian experiment without recognizing it. This terrestrial toad descended from aquatic ancestors that grow roughened ridges on their forefeet—the nuptial pads. Males use these pads to hold the female while mating in their slippery environment. Midwife toads, copulating on terra firma, have lost the pads, although a few anomalous individuals do develop them in rudimentary form—indicating that the genetic capacity for producing pads has not been entirely lost.
Kammerer forced some midwife toads to breed in water and raised the next generation from the few eggs that had survived in this inhospitable environment. After repeating the process for several generations, Kammerer produced males with nuptial pads (even though one later received an injection of India ink, perhaps not by Kammerer, to heighten the effect). Kammerer concluded that he had demonstrated a Lamarckian effect: he had returned the midwife toad to its ancestral environment; it had reacquired an ancestral adaptation and passed it on in genetic form to offspring.
But Kammerer had really performed a Darwinian experiment: when he forced the toads to breed in water, only a few eggs survived. Kammerer had exerted a strong selection pressure for whatever genetic variation encourages success in water. And he reinforced this pressure over several generations. Kammerer’s selection had gathered together the genes that favor aquatic life—a combination that no parent of the first generation possessed. Since nuptial pads are an aquatic adaptation, their expression may be tied to the set of genes that confer success in water—a set enhanced in frequency by Kammerer’s Darwinian selection. Likewise, the ostrich may first develop callosities as a nongenetic adaptation. But the habit of kneeling, reinforced by these callosities, also sets up new selective pressures for the preservation of random genetic variation that may also code for these features. The callosities themselves are not mysteriously transferred by inheritance of acquired characters from adult to juvenile.
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