Ethics of the Abyss by Denys Spirin - HTML preview

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​Chapter 10

One may suggest that ontoviruses, once established, can become permanent; that a sufficiently well-fed, well-protected ontoviral system should persist indefinitely. History says otherwise. No ontovirus has ever achieved permanent stability. They all either fragment or die.

Christianity began splitting within decades of its founding. The Pauline version displaced the Judaic-Christian one; the Great Schism divided East from West; the Reformation shattered the West into a thousand pieces. Two millennia of continuous feeding, billions of ritual performances, an institutional apparatus of staggering sophistication — and the result is proliferation. The same Christianity that was one in the fourth century has thousands of denominations today.

Marxism followed the same arc in compressed time: a unified theory in 1848, a dozen warring factions by 1960. Liberalism is fracturing right now. Other ontoviruses skip fragmentation and go straight to extinction — local belief systems vanishing by the hundreds, political regimes collapsing within a generation when the feeding apparatus is destroyed. Fascism, Nazism, Khmer Rouge communism: postulates that seemed to their carriers like the foundations of reality evaporated almost overnight.

The parallel with evolutionary processes is striking in this context. A biological species fragments when a population encounters divergent environmental pressures. Geographical isolation produces genetic drift; over time, the populations become incompatible. The mechanism requires three elements: variation, selection, and isolation.

Variation arises because every host is a unique experiential substrate. A subject who receives an ontovirus already carries his own history and previously installed ontoviruses. The same postulate, absorbed by two different subjects, becomes two postulates — it lands on new soil and fuses with unique material. A fourth-century monk and a sixteenth-century merchant both receive "God is love," but the monk's version is saturated with desert asceticism and Neoplatonic cosmology, while the merchant's is filled with contractual obligation and printed catechism. Occasionally, a mutation hits a postulate that matters, and a viable variant emerges: Lutheranism, Leninism, Reform Judaism. The variant is close enough to the parent to compete for the same hosts and diverse enough to offer a distinct normativity.

Selection works through the feeding mechanism. An ontovirus survives by extracting ritual performance from its carriers. Any variant that does that more efficiently in a given environment outcompetes variants that do not. Calvinism outcompeted Catholicism in early-capitalist Northern Europe because it aligned better with the emerging economic order: individual responsibility, the sanctification of labor. Catholicism persisted in agrarian Southern Europe, where its communal rituals and hierarchy still matched the institutional landscape.

Once a variant has established itself in a distinct environment (a different country, for example), the population of carriers ceases to exchange ontoviral material. The Catholic and the Protestant read different books, attend their own rituals, and raise their children inside specific ethical frameworks. Within a few generations, the variants become incompatible and speciation is complete.

Fragmentation, then, is ontoviral mutation. It is the inevitable consequence of imprecise transmission under divergent selection pressures. The surprise is that any ontovirus holds together at all — and indeed the ones that do hold longest are those that have evolved the most rigorous mechanisms of transmission fidelity: catechisms, creeds, standardized liturgies, and inquisitions. Each of these is the equivalent of a proofreading enzyme — a mechanism that reduces the mutation rate by catching deviations before they propagate.

The Catholic Church's institutional genius lies here: a centralized authority that standardizes doctrine, a ritual calendar that synchronizes practice across continents, and a dedicated apparatus (the Congregation for the Doctrine of the Faith, formerly the Inquisition) whose sole function is to identify and eliminate variants before they reach reproductive viability. This machinery slowed the mutation rate for fifteen centuries.

Extinction, correspondingly, is the ontoviral equivalent of a species losing its ecological niche. An ontovirus becomes extinct when the environment that sustained its feeding cycle disappears. Fascism died because the regulatory apparatus was physically destroyed. The postulates persist in books, in memories, the way a species might linger as a handful of individuals in a zoo, but the reproductive cycle has been broken. A generation of non-performance, and the ontovirus exists only as an archival specimen: readable but inert.

Biological extinction is permanent. A species, once gone, does not return. Ontoviral extinction is reversible — the postulates, unlike genes, can be stored in text and recovered. Nazism is extinct as a living ontovirus; but the doctrine survives in libraries, and under the right conditions a new ontovirus can assemble itself from the archived material. It will resemble the original the way a reconstruction resembles the extinct animal: ecologically functional but assembled from contemporary components. Neo-fascist movements are ontoviral reconstructions: they install the archived principles into a new feeding apparatus (online platforms, meme-based transmission). The Hermetic revival of the Renaissance was exactly this: a set of dormant Hellenistic ontoviruses, preserved in manuscripts, reactivated when the governing structures of late-medieval Italy provided a suitable ground.

In biology, genetic material flows vertically, from parent to offspring. Horizontal gene transfer exists (bacteria do it routinely) but is the exception in complex organisms. In ontoviral evolution, horizontal transfer is the norm. A subject raised inside one ontovirus can acquire material from another through reading, conversation, migration, or conversion. The resulting hybrid may be unstable: two incompatible normative grids running on the same host, producing guilt and confusion. Or it may be viable: a new synthesis that combines postulates from multiple sources. Christianity itself was such a hybrid — Judaic monotheism crossed with Hellenistic philosophy and Roman institutional practice, assembled over three centuries of horizontal transfer into an organism that could outcompete its parents.

The evolutionary framework also explains the arms race between ontovirus and host. Biological parasites evolve to exploit hosts more efficiently; while hosts build resistance. Ontoviruses face the same pressure. A population exposed to a particular ontovirus for long enough develops a degree of immune response — the rituals lose their charge, and the feeding cycle weakens. The Enlightenment was, among other things, a host resistance event: a population of European intellectuals who had been exposed to Christian ontoviruses for so many generations that the postulates had become transparent. The opposition took the form of critique, philosophy, science, and satire, making the core vulnerable. The ontovirus responded by evolving: liberal Christianity, deism, and secular humanism — variants that retained the feeding mechanics (guilt, epistemic authority) while shedding the postulates that had become obsolete. A wave of critique produces a new strain of camouflaged ontoviruses, and the new generation eventually provokes a fresh wave of critique.

The question of agency is the one that the evolutionary framework does not address. Biological evolution is blind; organisms compete, genes replicate, and adaptation occurs unintentionally. Ontoviral evolution can be described in the language of will. We say that Christianity wants to convert the heathen, and the nation strives to expand its borders. An ideology seeks to dominate. Want, strive, seek, resist — the verbs of agency, applied to entities that are nothing more than sets of postulates.

This language is considered metaphorical in biology. Dawkins spent a book explaining that the "selfish gene" is a figure of speech: genes do not want anything, natural selection has no goals, and evolution is a blind process without intention or direction. The gene simply replicates, and the ones that replicate more effectively persist.

With ontoviruses, the situation is reversed. When we say that Christianity wants to convert the heathen, this is not a metaphor. There are real missionaries, campaigns, resources allocated, and specific strategies devised. When it is stated that an ideology seeks to dominate, there are propagandists, media, and institutions dedicated to exactly this purpose. The will is actual. But whose will is it?

The ontovirus is a set of postulates and a moral vocabulary. It does not have a nervous system and desires. It cannot want anything at all. Left alone on a shelf written in a book that nobody reads, encoded in a ritual that nobody performs, it is inert.

The will belongs to the carriers. The missionaries who cross oceans, the soldiers, the activists, the parents who raise their children inside the teaching — the will is theirs. Each of them experiences this will as his own.

This is what distinguishes the ontovirus from the biological virus, or gene. A virus hijacks the cell's replicative machinery, but it does not need the cell to believe in it, nor does it require the mind's active commitment or consent. The ontovirus needs all three: the host's cognitive and social apparatus, belief, and will.

The ontovirus is both more powerful and more fragile than any biological parasite. A host who wants to serve is more effective than one who only carries. The human inhabited by an ontovirus produces crusades, constitutions, cathedrals, and revolutions. However, it is more fragile because the will can be withdrawn. A gene cannot decide to stop replicating, but a will that has been given can be taken back. The entire edifice of the ontovirus rests on the host's continuous, moment-by-moment delegation of his will to the system.

The host does not lose his will; this is not possession. He lends it. He experiences the ontovirus's objectives as his own goals, its prohibitions as his own conscience. The will remains his; what has shifted is the criteria it serves. This is delegation in the precise sense: the authority to decide what matters has been transferred to the system, while the energy of execution remains with the subject.

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