V
The fact that the stimulus-receiving cortical layer lacks any shield protecting it against excitations from within must presumably mean that these stimuli acquire greater economic importance, and often give rise to economic dysfunctions, which are equatable with traumatic neuroses. The most abundant sources of such excitation from within are the organism's so-called drives, which represent all those manifestations of energy that originate in the inner depths of the body and are transmitted to the psychic apparatus – and which are themselves the most important and the most inscrutable element of psychological research.
We shall perhaps not think it too bold to suppose that the impulses deriving from the drives adhere not to the ‘annexed’ type of nervous process, but rather to the type that is free-flowing and constantly pressing for release. The best information we possess concerning these processes comes from our study of dream-work. We found that the processes in the unconscious systems are fundamentally different from those in the (pre-) conscious ones; that within the unconscious, cathexes can easily be completely transferred, displaced, compressed – something that could only produce flawed results if applied to pre-conscious material, and indeed for that very reason produces the familiar peculiarities of manifest dreams, the pre-conscious residua of the preceding day having been processed according to the laws of the unconscious. I termed this kind of process in the unconscious the ‘primary’ psychic process, in contradistinction to the ‘secondary’ process that obtains in our normal waking life. As the drive-impulses all act on our unconscious systems, it is scarcely a new departure to assert that they follow the primary process, and it is also no very great step to identify the primary psychic process with Breuer's ‘free-flowing’ cathexis, and the secondary one with his ‘annexed’ or ‘tonic’ cathexis.33 This would then mean that it was the task of the higher echelons of the psychic apparatus to annex excitations originating from the drives and reaching it via the primary process. Any failure of this annexion process would bring about a dysfunction analogous to traumatic neurosis. Only when the annexion has taken place would the pleasure principle (or, once the latter has been duly modified, the reality principle) 34 be able to assert its dominion unhindered. In the meantime, however, the psychic apparatus's other task of controlling or annexing the excitation would be very much to the fore – not, it is true, in opposition to the pleasure principle, but independently of it, and to some extent quite heedless of it.
The manifestations of a compulsion to repeat that we have described with respect to the early activities of the infant psyche, and also with respect to our experiences in the course of psychoanalytic practice, plainly bear the stamp of drives, and wherever they are in opposition to the pleasure principle they equally plainly exhibit their daemonic character.35 In the case of children's play it seems readily comprehensible to us that the child also repeats unpleasurable experiences, because by thus being active he gains far more thorough-going control of the relevant powerful experience than was possible when he was merely its passive recipient. Each new repetition seems to add to the sense of command that the child strives for; and in the case of pleasurable experiences, too, the child never tires of repeating them, and will be implacable in insisting that every experience is identical to the first. This trait is destined to disappear later on: a joke will fall flat at the second time of hearing; a play will never again make the same impression that it did on first viewing; indeed it would be difficult to get an adult to re-read a much-enjoyed book until considerable time had elapsed. Novelty will always be the precondition of enjoyment. The child, however, will never tire of requiring adults to repeat a game that they showed him or played with him, until they refuse out of sheer exhaustion. And once anyone has told him a nice story, he wants to hear the same story again and again rather than a new one; he implacably insists that every repetition be exactly the same; and he corrects every least change that the story-teller misguidedly incorporates, perhaps fondly imagining it will gain him extra kudos. In this, the pleasure principle is not being contradicted; it is evident that the repetition, the replication of the original experience in identical terms, itself represents a source of pleasure. In the case of analysis, on the other hand, it becomes clear that the compulsion to repeat the events of infancy in the transference process flouts the pleasure principle in every way. The patient behaves in a completely infantile manner, and thus shows us that the repressed memory traces of his primal experiences are not in an annexed state, indeed are to all intents and purposes incapable of secondary processing. It is this non-annexed state, moreover, that accounts for their ability to form a wish-fantasy36 by latching on to the residua of the day, a fantasy that finds expression in dreams. The same compulsion to repeat very often confronts us as an obstacle to therapy when at the end of a patient's course of treatment we seek to bring about his complete disattachment from the physician; and we may reasonably suppose that the turbid fear of patients unfamiliar with analysis, who shrink from reawakening something that in their view is best left dormant, essentially reflects their dread of seeing this daemonic compulsion make its appearance.37
But what is the nature of the connection between the realm of the drives and the compulsion to repeat? At this point we cannot help thinking that we have managed to identify a universal attribute of drives – and perhaps of all organic life – that has not hitherto been clearly recognized, or at any rate not explicitly emphasized. A drive might accordingly be seen as a powerful tendency inherent in every living organism to restore a prior state, which prior state the organism was compelled to relinquish due to the disruptive influence of external forces; we can see it as a kind of organic elasticity, or, if we prefer, as a manifestation of inertia in organic life.38
This conception of drives sounds strange, for we have become accustomed to seeing drives as the key factor pressing for change and development, and now we are supposed to see them as the direct opposite: as the expression of the conservative nature of organic life. On the other hand it doesn't take us very long to think of examples in the animal world that seem to confirm that drives are indeed historically determined. When certain kinds of fish undertake arduous journeys at spawning time in order to lay their eggs in particular waters, far from their normal habitat, then in the view of numerous biologists they are simply returning to the previous domain of their species, which, in the course of time, they have exchanged for others. The same is said to apply to the migration of birds; but we have no need to search around for further examples once we remember that the phenomena of heritability and the facts of embryology offer us the most spectacular proofs of the existence of an organic compulsion to repeat. We see how in the course of its development the embryo of any existing animal is compelled to repeat – albeit in the most fleeting and abbreviated way – the structures of all the forms from which the animal is descended, instead of hurrying by the shortest route to its definitive shape; and given that we can explain this behaviour scarcely at all in mechanical terms, we have no call to disregard the historical explanation. And we similarly find a reproductive faculty extending far into the higher echelons of the animal kingdom whereby a lost organ is replaced through the creation of a new one altogether identical to it.
Some consideration must doubtless be given to the evident objection that as well as the conservative drives that compel repetition, there may also be others that press for new forms and for progress; indeed, we shall take account of this objection later in our discussions. But in the meantime we may find it enticing to pursue the hypothesis that ‘all drives seek to restore a prior state’ right through to its logical conclusion. While the outcome of this might seem airy-fairy or reminiscent of the mystical, we are none the less confident in the knowledge that no one can accuse us of intending such an outcome. We seek the sober results of research or of reflections founded on research, and we seek to impart to these results no other quality but that of reliability.39
If, then, all organic drives are conservative, h
istorically acquired, and predisposed to regression and the restoration of prior states, we must accordingly ascribe the achievements of organic development to external influences and their disruptive and distracting effects. On this view, the elementary organism did not start out with any desire to change, and given the continuance of the same circumstances would have constantly repeated the selfsame life-cycle; but in the final analysis, so the argument goes, it must be the developmental history of our planet and its relationship to the sun that has left its imprint for us to behold in the development of organisms. The conservative organic drives have assimilated every one of these externally imposed modifications of the organism's life-cycle and duly preserved them in order to repeat them, and therefore inevitably give the misleading impression of being forces bent on change and progress, whereas they merely seek to achieve an old goal by new means as well as old. And this ultimate goal of all organic striving may be equally susceptible of definition. It would contradict the conservative nature of drives if it were the goal of life to achieve a state never previously attained to. Rather, it must aspire to an old state, a primordial state from which it once departed, and to which via all the circuitous byways of development it strives to return. If we may reasonably suppose, on the basis of all our experience without exception, that every living thing dies – reverts to the inorganic – for intrinsic reasons, then we can only say that the goal of all life is death, or to express it retrospectively: the inanimate existed before the animate.
At some point or other, the attributes of life were aroused in non-living matter by the operation upon it of a force that we are still quite incapable of imagining. Perhaps it was a process similar in essence to the one that later, at a certain level of living matter, gave rise to consciousness. The tension generated at that point in previously inanimate matter sought to achieve equilibrium; thus the first drive came into existence: the drive to return to the inanimate. At that stage death was still easy for living matter; the course of life that had to be gone through was probably short, its direction determined by the newly created organism's chemical structure. In this way living matter may have experienced a long period of continual re-creation and easy death, until decisive external factors changed in such a way that they compelled still-surviving matter to take ever greater diversions from its original course of life and ever more complex detours in achieving its death-goal. These detours on the path to death, all faithfully preserved by the conservative drives, may well be what gives us our present picture of the phenomena of life. If one holds fast to the notion that the drives are exclusively conservative in nature, one cannot arrive at any other logical postulates concerning the origin and goal of life.
These conclusions may seem disturbing, but so too is the picture that emerges in respect of the great groups of drives that we posit behind the vital phenomena of organisms. The theory that there are drives directed at self-preservation, drives that we ascribe to all living beings, stands in striking opposition to the hypothesis that the entire life of the drives serves to procure death. Considered in this light, the theoretical significance of the drives concerned with self-preservation, self-assertion and dominance diminishes greatly. They are indeed ‘partial’ drives,40 charged with the task of safe-guarding the organism's own particular path to death and barring all possible means of return to the inorganic other than those already immanent; but the baffling notion of the organism striving to endure in defiance of the entire world – a notion incapable of being fitted into any sensible nexus – simply evaporates. The fact that remains is that the organism wants only to die in its own particular way; and so these guardians of life, too, were originally myrmidons of death.41 Thus arises the paradox that the living organism resists in the most energetic way external influences (‘dangers’) that could help it to take a short cut to its life's goal (to short-circuit the system, as it were); but it is precisely this sort of behaviour that characterizes purely drive-engendered strivings as against those of intelligence.
But if we really think about it, this cannot be true! Things take on a quite different aspect in the light of the sexual drives, to which neurosis theory has attached particuler importance. Not all organisms have yielded to the external pressure impelling them to ever greater development. Many have succeeded in remaining at their own lowly level right into the present time; indeed, there are many living things still in existence today that must resemble, if not all, then at least many of the early stages in the development of the higher animals and plants. And by the same token, not all the individual organic elements that make up the complex body of a higher organism stay with it throughout the entire course of its development to the point of natural death. Some of them, the germ-cells, probably retain the original structure of living matter, and after a certain period they separate off from the organism, carrying with them the full gamut of inherited and newly acquired drives. It is perhaps precisely these two characteristics that enable these cells to have an independent life. Given favourable circumstances, they begin to develop, i.e. they repeat the game to which they owe their own existence, and the outcome of this is that one portion of their matter continues its development right through to the end, while another reverts once more to the beginnings of the development process as a new germ particle. These germ-cells thus work in opposition to the death of living matter, and succeed in giving it what in our eyes must seem like potential immortality, while in reality perhaps signifying merely an extension of the dying process. We attach the greatest possible significance to the fact that the germ-cell acquires the strength, not to say the actual ability to achieve this feat only by merging with another germ-cell similar to it and yet different.
The drives that take charge of the destiny of these organic elements that outlive the larger entity, keep them safe while they are vulnerable to the stimuli of the external world, and bring about their encounter with the other germ-cells – these constitute the group termed sexual drives. They are conservative in the same sense that the others are in that they reincorporate previous states of the relevant living matter, only to a more marked degree inasmuch as they show themselves to be particularly resistant to external influences; and they are also conservative in a further sense, since they preserve life itself for longer periods.42 They constitute the true life-drives; and the fact that they act against the intent of the other drives, an intent that by its very nature conduces to death, points to a conflict between them and the rest, the importance of which was recognized very early on by neurosis theory. It amounts to a kind of fluctuating rhythm within the life of organisms: one group of drives goes storming ahead in order to attain the ultimate goal of life at the earliest possible moment, another goes rushing back at a certain point along the way in order to do part of it all over again and thus prolong the journey. But even though sexuality and gender differentiation were assuredly not present when life began, it none the less remains possible that the drives that subsequently merited the term ‘sexual’ were active from the very beginning, and that it was not only at some later stage that they began to counter the antics of the ‘ego drives’.43
Let us go back for a moment ourselves and ask whether all these speculations are not perhaps entirely baseless. Are there really no other drives apart from the sexual drives that seek to restore a prior state, nor others again that strive for a state never previously attained to? I know of no reliable example in the organic world that contradicts the picture that we have suggested. There seems to be no clear evidence of a universal drive favouring higher development within the animal and plant worlds, even though it remains an undisputed fact that developments do in fact proceed in that direction. But for one thing, it is in many cases merely a matter of subjective judgement when we declare one level of development to be ‘higher’ than some other; and for another thing, biology shows us that higher development in one particular respect is very often paid for or balanced out by regression in another. Moreover, there are plenty of animal forms whose early stages cl
early reveal that they have developed regressively rather than progressively. Higher development and regression might both be the result of the pressure to adapt exerted by external forces, and the role of the drives might be limited in both cases to the task of assimilating the imposed change as an inner source of pleasure.44
Many of us, too, may find it difficult to abandon the belief that there is in mankind itself an inherent drive towards perfection that has brought human beings to their present high level of intellectual attainment and ethical sublimation, and that can be relied on to ensure their further development to the status of Übermensch. For my own part, however, I do not believe in any such inner drive, and can see no way of salvaging this agreeable illusion. The development of mankind thus far appears to me to call for no other explanation than that applicable to animals; and the restless urge for ever greater perfection that we observe in a minority of individual human beings can readily be understood as resulting from the repression of drives – the foundation on which all that is most precious in human civilization is built. The repressed drive never abandons its struggle to achieve full gratification, which would consist in the repetition of a primary gratification experience. All the sublimations and reaction-formations and surrogate-formations in the world are never enough to resolve the abiding tension; and the gulf between the level of gratificatory pleasure demanded and the level actually achieved produces that driving force that prevents the individual from resting content with any situation he ever contrives, and instead – as the poet says – he ‘presses ever onward unbridled, untamed’ (Mephisto in Faust I, ‘Faust's Study’). The way back, the way to full gratification, is usually blocked by the resistances that keep the repressions fully active, and there is accordingly no alternative but to proceed in the one direction still available, namely that of development – though without any prospect of bringing the process to a conclusion and attaining the desired goal. The pattern of events during the formation of a neurotic phobia (which is nothing other than an attempt to evade the gratification of a drive) offers us a model exemplifying the genesis of this seeming ‘drive for perfection’, which, however, we cannot possibly attribute to all individual human beings. The dynamic conditions for the phenomenon are indeed universally present, but the economic circumstances appear to favour it only in rare cases.
Beyond the Pleasure Principle and Other Writings Page 12
