Read Beyond the Pleasure Principle Online
Authors: Sigmund Freud
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.
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If, then, all organic drives are conservative, historically 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,
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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.
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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.
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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’.
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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 clearly 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.
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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.
However, we would draw attention here, albeit very briefly, to the fact that, having rejected the ‘perfection drive’, we can probably find a replacement in the striving of Eros to concentrate organic matter in ever larger units.
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Taken in conjunction with the effects of repression, it could well account for the phenomena attributed to the ‘perfection drive’.
There are no doubt many respects in which we ourselves are going to feel dissatisfied with our conclusions thus far, which posit a sharp contrast between the ‘ego drives’ and the sexual drives, and argue that the former are bent on death, the latter on the continuation of life. Furthermore, it was really only the
former
that we could claim showed the conservative character of drives or – better – their regressive character, corresponding to the compulsion to repeat. For according to our hypothesis, the ego drives arise when inanimate matter becomes animate, and set out to restore the inanimate state. In the case of the sexual drives, on the other hand, they clearly
do
reproduce the primitive states of the organism – but the goal they strive for with all the means at their disposal is the merging of two germ-cells that are differentiated in a particular way. If this union does not come about, then the germ-cell dies, just like all the other elements of multicellular organisms. Only in this one circumstance can the sexual function extend life and confer upon it a semblance of immortality. But what important event in the developmental history of living matter is being repeated by sexual reproduction or by its precursor, the conjugation of two individual organisms amongst the protista? We do not know the answer to this question, and would therefore find it a considerable relief if our entire theory were to prove wrong. The antithesis of ego drives (death drives) and sexual drives (life drives) would then lose all validity, and at the same time the compulsion to repeat would lose the significance that we have attached to it.
Let us therefore go back to one of the postulates woven into our argument, in the confident expectation that it will lend itself to
complete rebuttal. We based a whole variety of conclusions on the presupposition that all living matter dies for reasons that are
intrinsic
to it. We made this assumption so blithely because it does not appear to us to
be
an assumption. It is our habit of mind to think in these terms, and the habit is reinforced by our poets and playwrights. Perhaps we have decided to embrace this belief because it brings us comfort. If we are to die ourselves, having first lost to death all those most dear to us, then we prefer to succumb to an implacable law of nature, the majestic 'Avάγχη [‘necessity’], rather than to a chance event that might well have proved avoidable. But perhaps this belief that death has its own intrinsic logic is simply one of the illusions we have created for ourselves in order to be able to ‘bear the heavy burden of existence’.
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It is certainly not primal: the idea of ‘natural death’ is alien to primitive peoples, who attribute every death that occurs amongst them to the influence of an enemy or an evil spirit. To investigate this belief, therefore, let us turn without further ado to biological science.