The Variation of Animals and Plants under Domestication — Volume 2 — Inside the Classic
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Hysterics was put to a son of Bedlamite, "but the result of the fifth cross is not as yet, I believe, more satisfactory than that of the fourth." On the other hand, with sheep, Fleischmann (15/13. As quoted in the 'True Principles of Breeding' by C.H. Macknight and Dr. H. Madden 1865 page 11.) shows how persistent the effects of a single cross may be: he says "that the original coarse sheep (of Germany) have 5500 fibres of wool on a square inch; grades of the third or fourth Merino cross produced about 8000, the twentieth cross 27,000, the perfect pure Merino blood 40,000 to 48,000." So that common German sheep crossed twenty times successively with Merino did not by any means acquire wool as fine as that of the pure breed. But in all cases, the rate of absorption will depend largely on the conditions of life being favourable to any particular character; and we may suspect that there would be a constant tendency to degeneration in the wool of Merinos under the climate of Germany, unless prevented by careful selection; and thus perhaps the foregoing remarkable case may be explained. The rate of absorption must also depend on the amount of distinguishable difference between the two forms which are crossed, and especially, as Gartner insists, on prepotency of transmission in the one form over the other. We have seen in the last chapter that one of two French breeds of sheep yielded up its character, when crossed with Merinos, very much more slowly than the other; and the common German sheep referred to by Fleischmann may be in this respect analogous. In all cases there will be more or less liability to reversion during many subsequent generations, and it is this fact which has probably led authors to maintain that a score or more of generations are requisite for one race to absorb another. In considering the final result of the commingling of two or more breeds, we must not forget that the act of crossing in itself tends to bring back long-lost characters not proper to the immediate parent-forms.
With respect to the influence of the conditions of life on any two breeds which are allowed to cross freely, unless both are indigenous and have long been accustomed to the country where they live, they will, in all probability, be unequally affected by the conditions, and this will modify the result. Even with indigenous breeds, it will rarely or never occur that both are equally well adapted to the surrounding circumstances; more especially when permitted to roam freely, and not carefully tended, as is generally the case with breeds allowed to cross. As a consequence of this, natural selection will to a certain extent come into action, and the best fitted will survive, and this will aid in determining the ultimate character of the commingled body.
How long a time it would require before such a crossed body of animals would assume a uniform character within a limited area, no one can say; that they would ultimately become uniform from free intercrossing, and from the survival of the fittest, we may feel assured; but the characters thus acquired would rarely or never, as may be inferred from the previous considerations, be exactly intermediate between those of the two parent-breeds. With respect to the very slight differences by which the individuals of the same sub-variety, or even of allied varieties, are characterised, it is obvious that free crossing would soon obliterate such small distinctions. The formation of new varieties, independently of selection, would also thus be prevented; except when the same variation continually recurred from the action of some strongly predisposing cause. We may therefore conclude that free crossing has in all cases played an important part in giving uniformity of character to all the members of the same domestic race and of the same natural species, though largely governed by natural selection and by the direct action of the surrounding conditions.
ON THE POSSIBILITY OF ALL ORGANIC BEINGS OCCASIONALLY INTERCROSSING.
Darwin opens Volume 2 with a dense chapter on reversion, or atavism, immediately establishing that inherited traits can reappear after generations of absence. He distinguishes reversions in pure breeds—such as pigeons and hornless cattle—from those in crossed varieties, and notes that the act of crossing itself can trigger the reappearance of latent characters. The chapter headings alone reveal a methodical structure: each topic is announced in a full sentence, as if Darwin is building an argument step by step.
Readers should note how Darwin uses specific, named examples—Fenton wheat found on a pile of basalt, Chidham wheat from a hedge—to ground his theoretical claims. These are not anecdotes but evidence for a broader principle: that domestic organisms never stop varying under uniform conditions, and that the rate of variation can accelerate once a type begins to change.
Reversion as a Window into Latent Characters
Darwin devotes the first chapter to reversion, which he treats as a key to understanding inheritance. He catalogs cases where pure breeds revert to ancestral forms—for instance, pigeons and fowls that throw back to wild coloration—and argues that these reversions prove the existence of latent characters carried in the germ. The germ, he writes, is “a wonderful object” because it contains all the potential traits of both parents and ancestors.
He also examines reversion through bud-propagation and in segments of the same flower or fruit, showing that the phenomenon is not limited to sexual reproduction. A peloric flower, for example, may represent a reversion to an ancestral symmetry. Darwin’s method is to collect diverse instances and then infer a common cause, rather than to propose a mechanism he cannot observe.
Prepotency and the Limits of Inheritance
In the second chapter, Darwin introduces the concept of prepotency—the tendency of certain individuals or breeds to transmit their characters more strongly than others. He notes that prepotency can be stronger in one sex than the other, and that it sometimes depends on whether a character is visible in one breed and latent in the other. This idea helps explain why some crosses produce offspring that resemble one parent almost exclusively.
Darwin also discusses inheritance limited by sex, citing newly acquired characters in domesticated animals that are transmitted by only one sex, or lost by only one sex. He connects these observations to the principle of inheritance at corresponding periods of life, which he argues is crucial for embryology. The chapter ends with a summary of three chapters on inheritance, reinforcing the cumulative nature of his argument.
Crossing, Absorption, and the Formation of New Races
Darwin turns to crossing in the third chapter, explaining that free intercrossing obliterates differences between allied breeds. When two breeds commingle in unequal numbers, the more numerous absorbs the other, a process influenced by prepotency, conditions of life, and natural selection. He notes that all organic beings occasionally intercross, with apparent exceptions being rare.
He then examines characters that seem incapable of fusion—chiefly those that have suddenly appeared in an individual—and discusses how crossing can modify old races or create new ones. Some crossed races, he observes, breed true from their first production. The chapter also addresses the crossing of distinct species in relation to domestic races, a topic that would later become central to debates about speciation.
The Accumulative Action of Changed Conditions
In the later excerpts, Darwin argues that the influence of changed conditions accumulates over generations. New flowers introduced to gardens do not vary at first, but after several years they begin to show variation. He cites the Dahlia, Zinnia, and Swan River daisy as examples where the timing of variation was recorded. The principle, he says, is that “the more a type has entered into a state of variation, the greater is its tendency to continue doing so.”
Darwin also discusses whether domestic productions could become so habituated to their conditions as to cease varying. He concludes that they never are exposed to uniform conditions long enough, and that even the most anciently cultivated plants and animals still vary. The chapter on accumulative action reinforces his broader argument that variation is not random but follows patterns that can be studied empirically.
Readers approaching this volume for the first time will benefit from tracking Darwin’s use of concrete examples—each named variety or experiment serves as a test of a general principle. The book is not a narrative but a series of linked arguments, and the chapter headings function as a roadmap. Pay attention to how Darwin qualifies his claims: he often admits when evidence is incomplete or when a conclusion is tentative. This caution is part of his scientific method, not a weakness.
Reading Darwin’s patient notes on pigeon reversion, I remembered my grandmother’s gnarled hands sorting seed packets, her quiet claim that flowers “remember” their wildness. My childhood copy of Texas Flowers in Natural Colors — Inside the Classic carried that same tenderness—each bloom a small argument for persistence, not perfection. Both books feel like watching someone breathe life back into a stubborn, familiar soil.
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