| …the
mere presence in the dictionary of a word like “living” does not mean
it necessarily has to refer to something definite in the real world. –
Richard Dawkins. The Selfish Gene p.18 |
Our language has but one word that aptly describes the presence of
humans on earth—INFESTATION. In contemplating a thriving wilderness, we
observe a rich variety of species engaged in elaborate systems of
conflict and collaboration. Diversity, variation, and a formidable
complexity of inter-species relations characterize such vibrant
communities. But disease may strike. A plague of millions of identical
locusts defoliate a landscape overnight, or a swarming brood of mites
may encrust a green leaf, withering it at once. These horrific
burgeoning monocultures provide the closest analogs in nature to the
human presence on this planet. The rectilinear, asphaltic crust
extruded by industrial civilization replaces flowering diversity with
vacuous repetition. Monolithic and oppressive crystalline geometry
overwhelms the delicate fractal foliations of natural forms. An empty
parking lot at night, lit by buzzing lamps of metallic halides, summarizes our civilization—brutal, pointless and ugly.
But while the necessity of violently obliterating this infestation
could not be any more manifestly apparent to all beings possessed of
some sliver of moral or æsthetic sense, a just and reasonable curiosity
impels us to inquire into the origins of this horror. And here we shall
find out and uncover realities so shocking, so threatening to all the
assumptions upon which our activities and common aspirations are based,
that we shall be tempted to recoil in abject horror, like the
overcurious child who turns back some forest stone or log to reveal
gelatinous scurrying forms, bristling with inscrutable appendages. Yet
children we find often to be possessed of an admirable scientific
detachment, permitting them to inquire into narrow by-ways of new
thought cemented off to more learned investigators. And what is thought
but the traversing of worn paths laid out by our ancestors in the deep
structures of our language? And what is insight but the demolition of
false semantic categories erected by the arbitrary structures of our
language and culture?Language, the claw by means of which we seek to
apprehend reality, is also the diaphanous baffle that forbids us from
approaching it.
Of course, it is quite possible to
think of things for which your language has no words, or to entertain
non-linguistic conceptions. These feats, however, are a lot less likely
to be attempted, and far more difficult to manage than simply picking
up the linguistic tools at hand. Alexandra David-Neel notes somewhere
that the Tibetans have something like twelve distinct words for
consciousness. It would be foolish to assert that such a fact had no
bearing on the ease with which the speakers of Tibetan negotiated that
tricky ground.
The adequate and ample
explication of the true significance of the human infestation will
require that we undertake a re-evaluation of several basic linguistic
categories. The fact that the manifestly abominable nature of our
civilization is so completely unrecognized indicates that such a
re-evaluation is long overdue.
Intention in our
language is ascribed only to beings agreed to be conscious. An angry
student at a riot willfully hurls a rock at the police, whereas a stone
in an eroding stream bank merely falls into the water below. The
osmoregulation of molecules across the lipid membrane of cells is
considered to occur as the result of blind and inalterable physical
laws, but the organism composed of such cells is somehow commonly
supposed to act by means of a separate and distinct will, unrelated to
the parts of which it is composed. Innumerable, intractable, and
irresolvable difficulties arise in defining the oppositions “conscious
and unconscious” and “alive and dead.”

A
beached whale, incapable of movement or breath, is yet for some time
admitted to be alive, while an ice crystal growing with speed out
across a winter windowpane, reproducing its form in an intricate and
symmetrical pattern, is thought dead. A lounging hominid is said to
consciously select a television channel, but a termite colony is
thought to produce an enormous and elaborately constructed edifice,
complete with independently interjoining bridges and tunnels, while
wholly unconscious. When intention is ascribed to dead things in out
language, these statements are said to be merely figurative i.e.: your
hair wants cutting, the computer virus is trying to spread, the
floodwaters aggressively surged over the levee, the engine was
reluctant to start, and so on. But in what respect these dead and
figurative agents differ from our own brains, which are merely globules
of fatty tissue, is unclear. If we ascribe intention to humans, how
could it be denied to other primates, or indeed to other animals? The
evolution of animals may be traced back to bacteria, which we know to
have arisen from matter itself. A mature and responsible view of
evolution can not just ignore the problems that immediately arise in
vainly attempting to restrict consciousness and intention to a few of
its outermost branches. Consciousness and intention are inherent to
matter itself. It is extremely difficult for most people to accept this
fairly obvious fact about our reality because their conditioned
assumptions, their daily mundane experiences, and the very structures
of their language itself, all mitigate against it. How much more
difficult is it then to grasp a reality that entails the flagrant
contradictions of one’s basic linguistic categories! The train of
thought is reluctant to hurl itself from the rigidly established rails.
An indiscriminate pile-up threatens. But we must recall that our
linguistic categories, useful as they may be, have absolutely no real,
necessary or essential relation to the actual reality in which we find
ourselves. Crisp, inscrutable, vast and unfathomable, it notoriously
defies language.
As we would throw away a tool
that could neither grip nor interact with any mechanism in our
environments, let us

at last jettison these words, intention and
consciousness, which by remaining in our linguistic toolbox serve only
to prevent us from grasping our situation. But how are we to explain
the presence of these empty concepts in our linguistic arsenal? Are
they merely artifacts of out own limited abilities, convenient
shortcuts in navigating our daily reality? Or, instead, do they serve a
more sinister purpose, blinding us to certain forces that are farming
us out for their own purposes?
How useful would
it be to a jailer if his prisoners were prevented, not by iron bars and
granite walls, but by the very structures of their own language and
thought from ever contemplating escape! Perhaps it was more by
eliminating in them the concept of liberty, than by the construction of
corrals, sties, pens and leashes that animals were domesticated. The
fact is, the entirety of civilization, a foul smut blighting the fair
face of our planet, is essentially a vast factory farm being run by
entities to which our language prevents us from ascribing intention.
Chief among these are technology, hierarchical social systems, and
cheap scams being run out of the lower astral (religions).
But try suggesting to someone that their computer is using them, and
you will be met with sputtering incredulity. While the established
categories of our thought render such an idea outlandish and perverse,
an objective analysis of reality strongly suggests that agency, and
indeed intelligence, are inherent to all complex systems. How do these
things arise in our own brains, if they are not native attributes of
matter? It seems clear that will and intelligence, and indeed cunning
of the vilest sort, all arise out of matter itself. This view of
reality is an essentially magical one, applicable to belief systems
termed animist. Such systems of thought remain uninfected with false
distinctions between alive and
dead. Systems of thought labeling
themselves scientific or rational, are actually found to be wallowing
in the rankest superstition, unwilling to face the fact that
consciousness and will exist throughout matter. Cavernous voids of
unexamined self-contradiction lie below worldviews restricting agency
to humans. The investigator heedlessly torturing rodents in a lab,
despite his ostensible “scientific” detachment, is actually relying on
the most phantastical and baseless superstition to disguise the fact
that his unwilling laboratory assistants are as conscious as himself.
The human intellect in its pristine and undomesticated state easily
recognized this pansophistical reality. Yet at some point, something
began to cloud over these hitherto obvious facts. At what point? At the
beginning of civilization, when the process of domestication began. As
we shall see, when we domesticated plants and animals, something
domesticated us.

In medieval times, a view of
reality once prevailed, now characterized as “the great chain of
being.” This led upwards from mineral to vegetable, to human, angelic
and divine strata of existence. Alchemical engravings depicted these
realms as radiating out from a central core, the crude ball of earth
itself. In classical times, that great goddess Artemis of Ephesus, was
depicted as a glorious female being, ringed with breasts, arising out
of successive levels of minerals, vegetables and animals. Here let us
adopt that old system of thought, as we investigate the feats of
intelligence and will in the complex interactions of matter. From base
Physics we shall progress to Biology, that vast and scintillating field
of lights upon which we can most easily observe the interactions of
complex organizations of matter, commonly termed life. Nor shall we
draw a thick and arbitrary line between the biological and
anthropological realms, or between the dæmonic and the divine.
But this hierarchical chain of being serves also to disguise and
obscure from us a great truth, namely, that simpler, blinder, less
aware and even atavistic forms often dominate and control more complex,
mobile and outwardly evolved forms. A population of magnificent lions,
striding across the Serengeti, may be rigidly regulated by their
intestinal parasites. Submicroscopic viruses are often more responsible
for population dynamics than spectacular predators.
In attempting to understand the human infestation on earth, we must
first understand perhaps the single and central ruling dynamic of all
biological systems—Parasitism. Parasites are simply species that live
on or in another organism, and harm it. No parasitology text fails to
inform its readers, in its first paragraph, that the majority, or even
the vast majority of species are parasitic. In tracing the parasitic
lifestyle up through the chain of being, we will everywhere observe how
parasites control and farm out their host’s populations. An objective
view of human civilization will reveal us to be essentially a farmed
species. What are some of the characteristics of farmed animals? First:
large, crowded populations of redundant individuals, entailing the
concentration of waste products, with its attendant diseases. Second:
loss of wild attributes, such as self-reliance, endurance, and
especially awareness. Third: confinement into sties, cubicles, corrals
or enclosures. Fascinating morphological curiosities such as obesity
and the persistence of malformed individuals into adulthood are also
highly characteristic of domesticated animals. But while it is clear
who domesticated hogs or cattle, who domesticated humans?
When my housemate’s rabbits, raised for meat, escape from their cage,
they don’t wander far, but sadly seek only to re-enter their befouled
enclosure, encrusted with rotten shit, where the extruded pellets to
which they are accustomed are provided. Such is domestication—abject,
craven enslavement to bloodthirsty beings, a castration of possibility,
a sick lust for whatever foul pit most overflows with our own diseased
shit. While caged rabbits can have little conception of their masters
beyond a beneficial source of food and treats, just so do humans look
upon their parasitic overlords. Engorged hominids squeeze out of their
transport pods and mob the entrances of malls, lusting after the latest
electronics. Placed in the wild, they require rescue.
But let me restrain for a moment these delightful spasms of vitriolic
hyperbole. Let us take the deep view, the view corresponding to the
immense layered deposits of geological time. Let us seek to understand
the human infestation by tracing its parasitical roots back down the
great chain of being, back through animals to bacteria, to viruses and
at last to the molecular codons of life itself.
Biology
All species are complex arrangements of matter whose forms and
functions are controlled by their DNA, the spiral molecule that codes
for their constituent proteins. The DNA of a typical species contains
tens of thousands of base pairs. But if we are to look closely the
genetic code of any organism, a strange and striking fact will become
apparent: the vast majority of this DNA does not code for any protein,
and indeed has nothing to do with the expressed form and function of
the individual. This non-coding or “junk” DNA can take up almost the
entirety of a species genetic code. Something like 98% of human DNA is
non-coding. Junk DNA just gets pointlessly carried along from
generation to generation. Occasionally, the repetition of these vast
sequences of useless DNA goes awry and interferes with the coding DNA,
producing mutations. Francis Crick, co-discoverer of the DNA molecule
itself, was the first to suggest that these vast stretches of
non-coding DNA were essentially parasitic. This opinion has since
gained wider acceptance. So, just as the majority of organisms are
parasitic, so too is the majority of genetic code. The very book of
life itself largely consists of meaninglessly garbled and empty symbols
bearing no relation to the organism that carries them. These empty
codons reproduce solely for the sake of reproduction itself.
Before going on, let’s here address a crucial point. You might very
well ask why any organism reproduces but for the sake of reproduction
itself. Is there any other purpose for the reproduction of organisms
besides merely the blind and empty struggle of genes to replicate?
Perhaps, in the strictest sense, there is not. Yet I see a difference
between parasitic and independent organisms in what their life-process
seems to be striving towards. Parasitic beings are exclusively
concerned with reproducing themselves in their hosts, while independent
beings seem to be striving towards something else, something that
William Burroughs in a memorable essay termed “my own business”. This
ulterior goal seems to pertain to the unfoldment of latent potentials,
the development of new parts, and the extension of faculties of
awareness. Vision, freedom, and a sort of aspiration towards the
infinite differentiate independent from parasitic organisms. Those
latter tend to recede into blindness, atavism, loss of parts and
dwarfism. Their effect in populations is one of control, coercion and
prevention, hindrance and impediment.
It is of
course most unfashionable and politically incorrect to speak in such
terms. An egalitarian view of species is now favored. I am fully aware
of, and indeed overawed by the astounding intricacy and complexity of
many parasite morphologies and life cycles, from the thousands of
tapeworm attachment structures, to the fearsome strategies of the
parasitic wasps, the ghastly Ichneumonidæ. Yet while it would clearly
be unfair to term these triumphs of parasitic evolution as somehow less
“highly developed” than their hosts structures and strategies, and
setting aside any moralistic opprobrium that may attach in our culture
to a derivative and parasitic existence, I think it is still clear that
independent beings, in their struggle for existence, are perusing
something beyond mere replication – namely, the outward and
aspirational unfoldment of latent possibilities of autonomous
development and awareness, i.e.: “their own business.”
The DNA that does actually code for proteins builds some kind of
external structure or body in order to facilitate its own reproduction.
This structure may take the form of a fungus, an oak, a squid or you.
The majority of DNA, derisively termed “junk,” is merely along for the
ride. But, to take a parasitical view of the matter, could we not view
the coding DNA as a host inhabited, and to some extent perhaps designed
by its vaster parasite, the junk DNA? Peering into these deep
foundations of the phenomenon of life, we see that exploitation and
parasitic relations are the most basic blocks there, upon which the
vast superstructure of biology is erected. Parasitism is the cryptic
subtext in the book of life, which can be easily overlooked by a
superficial reader whose eye is drawn merely to the most flamboyant and
florid passages. The profounder critic reads another book in the same
covers, one layered with interfolded latencies of control and
exploitation.
Surely no joy could be greater
than to slay your enemy, crack open his skull, and greedily devour the
hot, limpid mush of his brains. But even this pure and simple source of
innocent delight is fraught with a parasitical peril, and one acting in
the sub-biological or molecular realms. Prions are misfolded molecules
which, once they enter the brain, somehow manage to replicate
themselves, eventually reducing that marvelous organ to a sagging
terrain of cratered rot. Mad cow disease, Kreutzfeld–Jacob disease, and
Alzheimer’s disease are all thought to be caused by prions. So is kuru,
the inevitably fatal malady of progressive brain rot, observed in the
highlands of Papua New Guinea, where ritual cannibalism was a popular
practice. Although the exact mechanics of prion action are far from
being understood, these pathogens indicate that the phenomenon of
parasitism extends down to the molecular realm.
The foul rupturing of crustulous pustules, the atrophy of limbs into
frail sticks, the spasmodic, convulsive ejaculation of mucosal
globules, threaded with blood, and the fevered gibbering of the
terminally diseased – all these familiar domestic occurrences are
provided for us by that “sub-microscopic, obligate, intercellular
parasite” the virus. Like certain other parasites we shall investigate
later, viruses enjoy the distinction of being powerful entities not
generally classified as being alive. They do not grow, but are
manufactured ready-made by their host cells. If ground up into bits,
they will re-assemble into the complete virus. In humans they cause
diseases like smallpox, polio, herpes, rabies, measles, mumps, AIDS,
SARS, Ebola, and the common cold. The author of Principles of Molecular
Virology proudly declaims “There is more biological diversity within
viruses that in all the rest of the bacterial, plant and animal
kingdoms put together. This is the result of the success of viruses in
parasitizing all known groups of organisms …”
A
virus is a small strip of DNA encased in a protein coat, to which some
sort of attachment or injection structure is frequently added. When the
viral DNA enters a host cell, the cell stops going about its own
business, and starts manufacturing viruses. Often the cell is destroyed
when the new viruses are released. This cell death leads to the
symptoms of disease in the host organism. Obviously, it cannot be in
the interest of the virus to kill or totally eradicate its host. Here
we come to the central goal for all parasites: achieving optimal
virulence. A parasite with suboptimal virulence is unable to fully
exploit its host population, while excessive virulence will eliminate
the host entirely. Newly emerged viral diseases in humans, like Ebola
hemorrhagic fever, are often excessively virulent. They kill their
hosts before the virus has been allowed to spread much. In contrast,
more established viruses, like the flu virus, generally allow plenty of
time for their hosts to go about spraying viruses everywhere. The
practical result of a parasite’s struggle to attain optimal virulence
is that the parasite is managing, controlling, and in fact farming out
its host population. This farming effect is one of the basic actions of
parasites. Farming is what parasites do. They seek to manage their
hosts with maximal economy. Their account books and ledgers are the
statistical permutations of natural selection.
Consider a human farmer of rabbits. Although the entire point of the
operation is to kill and eat the rabbits, he spends far more time
caring for them than he does killing them. Still, were he to lavish too
much care on them, perhaps by feeding them special delicacies,
caressing them and reading them bedtime stories, he would be easily
undersold by his rabbit farming neighbors. Were he to devote too little
time to the rabbits, they would either starve from neglect, or else be
buried in a conglobulated accumulation of their own pelleted shit.
In seeking a relationship of optimal virulence with its host, a
parasite is doing something similar to our rabbit farmer. Both their
livelihoods depend on the successful management of their host
populations. Since a rabbit farmer does not live inside his rabbits, he
is not termed a parasite, but he is still living a characteristically
parasitic existence. He might keep the rabbits confined, but he himself
cannot stray too far, or linger too long, from the cages he has set up.
In domesticating animals, he domesticates himself.
It is popularly imagined that viruses are the simplest pathogen, but
incredibly, even these simple entities can themselves be infected by
still smaller agents. These sub-viral parasites, termed virusoids, are
small RNA molecules that depend entirely on the presence of another
virus for replication. Their replication interferes with the function
of their host viruses, making them true parasites. Certain viral
diseases of plants are particularly vulnerable to virusoids, whose
effects are visible in the types of leaf damage caused. These minute
agents are the first example we encounter of hyperparasitism, or the
parasitization of parasites themselves. Hyperparasites indicate the
fearsome complexity of biological relations, in which a sort of fractal
parasitism can often be perceived. Infinitely unfolding and symmetrical
patterns of parasitism spring to life wherever we look. From these most
minute sub-elements of the microcosm, up to the vast planetary agencies
that dominate the earth, a single script is being played out.
Replication of forms through the exploitation of others is its keynote,
and domination, domestication and control are its themes. Everywhere a
gravitational lapse towards parasitism is evident. While all known
parasitic species presumably evolved from free forms, there are no
known examples of a parasite that evolved into a free-living form.
In passing from the viral to the bacterial realms, new aspects of the
farming and domesticating behavior of organisms become apparent. Most
parasitology texts are careful to make the distinction between
parasitic and mutualistic organisms. While both live within other
organisms, parasites harm (to a carefully modulated degree), and
mutualists help. Frequently cited examples of mutualistic life-forms
are the symbiotic algæ within corals or lichens, or the bacteria within
the digestive tracts of vertebrates that permit digestion to occur. The
more candid accounts, however, admit that “the distinction between
parasites and mutualists can become a headache.” It can be difficult to
determine who is exploiting whom. Some symbionts exploit their hosts,
some hosts their symbionts.
Around deep-sea
sulfur vents, far below the level where sunlight can penetrate, live
certain bivalve mollusks. In the absence of photosynthetic energy from
plants, these organisms feed on certain chemosynthetic bacteria that
live within their own flesh. While the mollusks provide a protected
environment in which the bacteria can live, they also kill the bacteria
in order to feed upon them. This is a very clear example of parasitic
farming relations, in which two species have become enslaved to each
other. One author mentions a laboratory experiment in which “a strain
of (free-living) Amœba proteus became infected with a parasitic
bacteria, and over a period of several years, the Amœbas became unable
to survive without that bacteria.” I met one unfortunate individual who
had lost 80 pounds while traveling in India, due to the massive chronic
diarrhea that he acquired there. He mentioned endless days spent lying
befouled on the floor of the bathroom of a cheap hotel, uncontrollably
spewing fœtid waste from all orifices. But when passing amateur nurses
gave him an antibiotic that killed off all his intestinal bacteria, he
assured me his condition then became even worse. I myself escaped from
that abominably foul nation, and from death itself, only with the aid
of many bed-ridden days of continual intravenous antibiotics. These
experiences left me with a renewed appreciation of our mutualistic
intestinal species.
With the sole exception of
the noble echinoderms, all animal phyla have evolved parasitic forms.
Some, such as the coelenterates have only one parasitic species, while
others, such as the Platyhelminths or flatworms, are mostly parasitic.
The worm phyla provide an excellent starting point for an investigation
of parasitic animals. The staggering fecundity of these parasites would
certainly merit reward from the Catholic or Mormon churches, could
these animals only be converted to those religions. The Ascaris species
of roundworm can lay 2,000,000 eggs per day, and their ovaries threaten
to rupture with 27 million developing eggs. These production
statistics, which would have aroused paroxysms of delight in Stalin or
Mao, have resulted in Ascaris infecting 1.4 billion humans. Yet
Hymenolepis diminuta, a tapeworm parasite of rats, can unleash up to
250,000 eggs each day, and 100,000,000 per year.

Let us linger here a while on the subject of tapeworms. These charming
animals, which often prove a source of amusement or diversion as they
crawl out the anus, mouth, or even the nostrils of our acquaintances,
reside in the intestines of vertebrates. Here they attain to prodigious
lengths. Tapeworms (Cestodes) consist of a head or scolex, beyond which
is a neck containing the stem cells that generate the proglottids or
reproductive segments. The scolex, often fearsomely armed with spines,
thorns and suckers, serves merely to attach the tapeworm to the
intestinal wall. There is no digestive or excretory apparatus at all.
Nutrition is obtained through absorption alone. The proglottids are
hermaphroditic, and can fertilize each other. “Immediately behind the
neck are the young proglottids, followed by mature, then gravid
proglottids. As new proglottids are formed in the neck, the previous
ones move posteriorly in a continuous process” Eventually the oldest
proglottids rupture, releasing eggs that are passed out with shit.
Entire proglottids observed in human craps were considered by ancient
and medieval philosophers to resemble melon seeds. Only with the dawn
of experimental science were these recognized as pertaining to
tapeworms.
That most august journal of the
heroic days of science, the Philosophical Transactions of the Royal
Society, documents progress on the cestodological front. Edward Tyson,
in the 1683 edition of that publication, corrected in his doubtlessly
enthralled readers, the view hitherto falsely held, that the wide end
of tapeworms was the head. He notes “a specimen of T. sagina, which he
obtained from a young man who ‘dragged it from himself, not without
some frightful apprehensions, that guts, and all, were coming out’; he
plainly perceived it alive, and to move: and having put it into a wide
mouthed glass it often endeavored by raising its body to get out.” Like
many parasites, tapeworms often require two hosts in their life cycles.
Once a tapeworm egg is eaten, it hatches and migrates in the body of
its first host before forming a podlike cyst. Only when the cyst-filled
meat is eaten can an adult tapeworm form in the secondary host.
Humans may obtain their own tapeworms by eating the cyst-filled flesh
of hogs or cattle. Pigs, notoriously coprophagic, provide an ideal way
for people to get tapeworms. When people ingest the tapeworm eggs, or
proglottids, the cysts form in human meat. The larval tapeworms exhibit
a decided preference for encysting in the brain. Perhaps the resultant
neurological damage increases the chances of the human being eaten by a
predator. At any rate, these tapeworm cysts in the brain are the
leading cause of epilepsy in humans worldwide.

How might a person chance to ingest a proglottid? Aside from those who
mitigate the tedium of their hours with protracted debaucherous bouts
of anilingus and coprophagia, ample opportunity for proglottid
ingestion abound. This possibility becomes understandable once one
grasps the enormous magnitude of proglottid production of which the
cestodes are capable. They have evolved the capability to continually
deluge their environments with eggs. While amazing reproductive
capabilities are characteristic of most parasites, the tapeworm is a
paradigm of fecundity, even in this overflowing field. Hexagonoporus
physeteris, a tapeworm parasite of sperm whales, can attain to lengths
of over 30 meters (100 feet), and have over 45,000 proglottids. Each
proglottid may have 4–14 complete sets of genitalia. With up to 630,000
independently functioning sets of genitalia, the Hexogonoprus
physeteris perhaps ranks as the sexiest animal on the planet.
Nevertheless, cryptopaleontologists are left to speculate on the
glorious lengths that may once have been attained by tapeworms in the
intestines of the largest dinosaurs. Parasites over a kilometer long,
fully capable of extruding billions of eggs per day, remain as a
tantalizing possibility. But perhaps far greater parasites exist today,
attached to human populations by means of a semantic scolex that
prevents us from recognizing autonomous agency in the institutions that
dominate our lives. Spreading over thousands of kilometers, infecting
billions of organisms at once, and resistant not only to eradication,
but to recognition, these parasites are the true factory farmers
engineering the human infestation now befouling our planet.
Organisms pursuing a parasitic lifestyle exhibit characteristic
morphological changes. In mollusks, these may include loss of shell,
reduction or disappearance of sense organs, disappearance of anus, and
then of the entire the digestive tract. They become progressively more
wormlike in shape. Absorption replaces digestion. Yet as the bodies of
these animals seem to be undergoing atavistic degeneration, their
lifestyles frequently sprout new and phantastic innovations. The life
of a predator (catch food and eat it) seems atrophied and dull compared
to the brilliant and profoundly cunning strategies parasites often
employ to reach new hosts.
The Dicrocoelium
trematode worm, whose secondary intermediate host is an ant, penetrates
into that animal’s brain and somehow makes it crawl up to the top of a
blade of grass and latch on. Here it is far more likely to be ingested
by a sheep, the main host. If no sheep comes by, the parasite retreats
and lets the ant go about its business for a day, before trying the
same trick the following night. Another trematode worm,
Leucochloridium, resembles a banded caterpillar. It enters its
intermediate host, a snail, and worms its way up into the poor animal’s
tentacles, where it proceeds to pulsate and gyrate in a colorful
display designed to attract a hungry bird, its main host. In a human
example, the Guinea worm Dracunculus, causes an extremely painful
burning ulcer to erupt on its host’s limb. Seeking relief, the infected
person goes to the nearest body of water to cool the inflammation. Upon
immersion, the freshly hatched juveniles are released into the water,
where they find their intermediate host, a copepod.
The annals of parasitology burgeon with similar accounts, each
exemplifying the profound and villainous cunning of these superficially
degenerated animals. Again and again, we find small unforbidding forms,
lacking even basic sense organs, manipulating their host’s behavior and
engineering their host’s populations for their own purposes of endless
reproduction. Accustomed to expect that anything damaging will be more
powerful than we are, we fail to perceive the forces that engineer our
own populations and dictate the details of our behavior. We seldom
expect to encounter cleverness in non-human, let alone non-animal
agents. Yet in truth, intelligence, will and downright villainous
cunning are inherent to all systems and their interactions. But before
rushing on to these human concerns, we must pay at least a brief call
to the arthropods, where gruesome and fascinating parasitological
narratives await.
At the family reunion of life
forms, the arthropods far outnumber all other classes. In grotesque
feats of ingestion and unfathomable depths of degeneracy these organism
likewise excel. The female cattle tick, Boophilus microplus, can drink
150 times its own weight in blood. Try as they might, even the most
ardent and dedicated consumers can seldom purchase, let alone ingest
such quantities of the extruded pellets upon which they feed. The
Pentastomida, or “toungeworms,” are an almost wholly inscrutable class
of parasites that infest the lungs of reptiles. It is unclear whether
they are indeed worms, or else some form of absolutely degenerated
arthropod, having lived sequestered in reptilian lungs since the
Triassic era. The latest speculation affirms that they are “probably a
very degenerate crustacean.” One hundred million years of parasitism
have reduced these animals to almost total estrangement from all other
forms of life. The intricate and fearsome arrays of vicious thorns with
which they are adorned have, however, endeared them to several of the
more morbidly inclined parasitologists of note.
Several arthropods also provide excellent examples of a parasite’s
ability to modify the behavior of its host. The Rizocephela, a
crustacean parasite of crustaceans, is one such animal. After a
“normal” youth, spent in a state in which it resemble a free-roving
barnacle larva, the parasite becomes “a living hypodermic syringe” that
seeks out a crab, its host. The Rizocephala injects itself into the
crab, where it becomes an “undifferentiated cell mass” It lacks a gut
and appendages (“not even reduced ones”) but “gets its nutrients by
means of root-like processes ramifying through the tissue of the crab
host.” Strange things then begin to happen to the crab, most notably
“parasitic castration.” “Various degrees of feminization appear in
subsequent instars.” In females, the result is hyperfeminization.
The
mechanism of host castration has yet to be explained … however, the
combined results of parasite structure and castration lead to an
astonishing diversion of host behavior to promote parasite survival.
The externa of the parasite is in the same position and is the same
size as the egg mass of the crab, as it would be carried on the crab’s
abdomen. Reacting as if the parasite were its own egg mass, the crab
protects, grooms and ventilates the parasite. If the grooming legs of
the host are artificially removed, the externa of the parasite soon
becomes fouled and necrotic. At the time the parasite begins to release
its larvæ, the crab performs spawning behavior. The parasites
apparently release pheromones that elicit larval release behavior in
the host crabs. And a final note: because they are castrated and
feminized, the male crabs also display appropriate maternal behavior!
The host departs from its normal hiding place, stands high on its legs,
and waves its abdomen back and forth. The naupuli (the earliest larval
stage) of the parasite are released into the current created by the
host.
The parasitic isopod Ancyroniscus bonnieri also feminizes its host.
After
infection of a definitive host Ancyroniscus bonnieri feed heavily, and
engorged isopods begin to produce eggs. During the process most of the
internal organs, including those of the digestive and nervous system,
disappear, and the animal becomes increasingly distended with eggs.
Finally all that is left is a large pulsatile sac of eggs that
ruptures, freeing the eggs
Eyeless, wingless
and flattened, armed with clinging claws and feeding on blood, mucus
and sloughed skin, able to attach their eggs to hair or feathers with
cement, lice have been a constant companion throughout human evolution.
The world record for lice removed from one person is over one thousand.
“Years of infestation lead to a darkened, thickened skin, a condition
called vagabond’s disease. In untreated cases of head lice, the hair
becomes matted together from exudate, a fungus grows, and the mass
develops a fetid odor. This condition is known as Plica Polonica. Large
numbers of lice are found under the mat of hair.” Obscure museums
preserve enormous specimens. How, you might ask, could anyone with a
six foot long enfungated monodread fail to instantaneously ameliorate
their situation by the simple expedient of cutting it off?
Superstition, we are told, was responsible for the preservation of
these moldy paradises for parasites. Similarly, Saint Simeon Stylites,
who spent 37 years living atop a pillar in the 5th century AD, was
widely lauded at the time for the solicitous and tender care with which
he deliberately re-attached to himself the lice that fell from his
body. Today on a sunny summer’s day, we may seen local hominids
diligently polishing their multiton transport pods, or hulking bloblike
on couches, absorbing programming, or even more likely, toiling in
cubicles under grim synthetic lighting. Lacking any distinct business
of their own, they do the business of their parasites.
But fleas, lice and ticks, merely external parasites, hold not half the
horror of the unspeakably repellant BOTFLY, a large pulsating larva,
ringed with sharp spines, that grows to grotesque magnitudes while
inextricably ensconced deep in human flesh. Amateur attempts at botfly
extraction generally fail, thwarted by the animal’s multiple rings of
spines. Panicked gringos at posh Costa Rican resorts reach in vain for
the forceps when the larval nature of the pulsating saclike
pustulosities in their pampered flesh becomes apparent. The mangled
remains of the mutilated grub rapidly putrify, opening into a
gangrenous, festering lesion, rank with oozing purulent matter. The
insufferable stench of flagrant rot precedes them as they come down to
breakfast, and irrepressible geysers of vomit mar the polished floors,
as executives and tycoons are treated to a gratuitous display of
hyperparasitsm.
Yet even these abominably
parasitized tourists get off easy, compared to children who get
botflies in their heads. Since the plates of their young skulls have
yet to grow together, the botflies are able to penetrate into the
brain, where they wax fat on the vehicle of thought itself. Death
follows for the fortunate, debility for those less so.

In this survey of the phenomena of parasitism from the molecular to the
animal realms, several significant trends have become apparent. First,
we commonly find simpler, blinder, more atavistic and less aware forms
controlling and farming out more complex and aware ones. Second, we
observe the amazing abilities of parasites to modify the behavior of
their hosts for their own purposes. Not content merely to passively
inhabit their host’s tissues, parasites can control all aspects of
their host’s behavior, hijacking the entire organism. Third, we notice
the care with which an effective parasite must manage its host
population. Excessive or insufficient virulence are alike detrimental
to parasites. A parasite that has attained optimal virulence is
analogous to a farmer who wisely manages the plants and animals on his
farm. Parasites farm their hosts. Finally, we note that the general
trend in parasite evolution is toward greater and more effective
attachment. While this may be achieved by all manner of hooks, thorns,
spines, suckers, or by deep burial within the host’s most vital
tissues, these merely external apparatus are less effective than the
ruses and deceits by which a parasite makes itself invisible to its
host’s often formidable immune system. This defense having been
circumvented, the parasite is able not merely to skim off the host’s
excess, but to use every aspect of the host’s body and behavior for its
own purposes. The host then becomes essentially an extension of the
parasite.
As we pass from the mineral,
vegetable, and animal, to the human, dæmonic and divine parasites, let
us keep these four dynamics in mind. We shall see them like luminous
worms, writhing and glowing, extending to obscene lengths as they
emanate from the foundations to the most exalted pinnacle of that vast
structure, the interaction of complex systems, Life.
next section- human parasites
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