northanger (northanger) wrote,
northanger
northanger

rhizosphere

AQ 246 = RHIZOSPHERE = ALPHA CENTAURI = ICHTHYOSAUR =
JULIUS EVOLA = MAGICAL ALPHABET = MESSENGER RNA = NECRONOMICON =
PATH OF VENUS = PRAXIS OF ART = SACRED LEMURS = SECRET RUNES =
SEVEN RISHIS = THOTHTODLANA = UAG AMBER (STOP)

A Thousand Plateaus: Capitalism and Schizophrenia

Gilles Deleuze + Felix Guattari

The abnormal clicking went on, beating out the dark, cosmic rhythm which underlies all mystical gate-openings—the Mechanosphre, or rhizosphere.

Principle of asignifying rupture: against the oversignifying breaks separating structures or cutting across a single structure. A rhizome may be broken, shattered at a given spot, but it will start up again on one of its old lines, or on new lines. You can never get rid of ants because they form an animal rhizome that can rebound time and again after most of it has been destroyed. Every rhizome contains lines of segmentarity according to which it is stratified, territorialized, organized, signified, attributed, etc., as well as lines of deterritorialization down which it constantly flees. There is a rupture in the rhizome whenever segmentary lines explode into a line of flight, but the line of flight is part of the rhizome. These lines always tie back to one another. That is why one can never posit a dualism or a dichotomy, even in the rudimentary form of the good and the bad. You may make a rupture, draw a line of flight, yet there is still a danger that you will reencoutner organizations that restratify everything, formations that restore power to a signifier, attributions that reconstitute a subject—anything you like, from Oedipal resurgences to fascist concretions. Groups and individuals contain microfascisms just waiting to crystallize. Yes, couchgrass is also a rhizome. Good and bad are only the products of an active and temporary selection, which must be renewed.

How could movements of deterritorialization and processes of reterritorialization not be relative, always connected, caught up in one another? The orchid deterritorializes by forming an image, a tracing of a wasp; but the wasp reterritorializes on that image. The wasp is nevertheless deterritorialized, becoming a piece in the orchid’s reproductive apparatus. But it reterritorializes the orchid by transporting its pollen. Wasp and orchid, as heterogeneous elements, form a rhizome. It could be said that the orchid imitates the wasp, reproducing its image in a signifying fashion (mimesis, mimicry, lure, etc.). But this is true only on the level of the strata—a parallelism between two strata such that a plant organization on one imitates an animal organization on the other. At the same time, something else entirely is going on: not imitation at all but a capture of code, surplus value of code, and increase in valence, a veritable becoming, a becoming-wasp of the orchid and a becoming-orchid of the wasp. Each of these becomings brings about the deterritorialization of one term and the reterritorialization of the other; the two becomings interlink and form relays in a circulation of intensities pushing the deterritorialization ever further. There is neither imitation nor resemblance, only an exploding of two heterogeneous series on the line of flight composed by a common rhizome that can no longer be attributed to or subjugated by anything signifying. Rémy Chauvin expresses it well: "the aparallel evolution of two beings that have absolutely nothing to do with each other." More generally, evolutionary schemas may be forced to abandon the old model of the tree and descent. Under certain conditions, a virus can connect to germ cells and transmit itself as the cellular gene of a complex species; moreover, it can take flight, move into the cells of an entirely different species, but not without bringing with it "genetic information" from the first host (for example, Benveniste and Todaro's current research on type C virus, with its double connection to baboon DNA and the DNA of certain kinds of domestic cats). Evolutionay schemas would no longer follow models of arborescent descent going from the least to the most differentiated, but instead a rhizome operating immediately in the heterogeneous and jumping from one already differentiated line to another. Once again, there is aparallel evolution, of the baboon and the cat; it is obvious that they are not models or copies of each other (a becoming-baboon in the cat does not mean that the cat "plays" baboon). We form a rhizome with our viruses, or rather our viruses cause us to form a rhizome with other animals. As François Jacob says, transfers of genetic material by viruses or through other procedures, fusions of cells originating in different species, have results analogous to those of "the abominable coupling dear to antiquity and the Middle Ages." Transversal communications between different lines scramble the genealogical trees. Always look for the molecular, or even submolecular, particle with which we are allied. We evolve and die more from our polymorphous and rhizomatic flus than from hereditary diseases, or diseases that have their own line of descent. The rhizome is an anti-genealogy.

The same applies to the book and the world: contrary to a deeply rooted belief, the book is not an image of the world. It forms a rhizome with the world, there is an aparallel evolution of the book and the world; the book assures the deterritorialization of the world, but the world effects a reterritorialization of the book, which in turn deterritorializes itself in the world (if it is capable, if it can). Mimicry is a very bad concept, since it relies on binary logic to describe the phenomena of an entirely different nature. The crocodile does not reproduce a tree trunk, any more than the chameleon reproduces the colors of its surroundings. The Pink Panther imitates nothing, it reproduces nothing, it paints the world its color, pink on pink; this is its becoming-world, carried out in such a way that it becomes imperceptible itself, asignifying, makes its rupture, its own line of flight, follows it's "aparallel evolution" through to the end. The wisddom of the plants: even when they have roots, there is always an outside where they form a rhizome with something else—with the wind, an animal, human beings (and there is also an aspect under which animals themselves form rhizomes, as do people, etc.). "Drunkenness as a triumphant irruption of the plant in us." Always follow the rhizome by rupture; lengthen, prolong, and relay the line of flight; make it vary, until you have produced the most abstract and tortuous of lines of n dimensions and broken directions. Conjugate deterritorialized flows. Follow the plants: you start by delimiting a first line consisting of circles of convergence around successive singularities; then you see whether inside that line new circles of convergence establish themselves, with new points located outside the limits and in other directions. Write, form a rhizome, increase your territory by deterritorialization, extend the line of flight to the point where it becomes an abstract machine covering the entire plane of consistency. "Go first to your old plant and watch carefully the watercourse made by the rain. By now the rain must have carried the seeds far away. Watch the crevices made by the runoff, and from them determine the direction of the flow. Then find the plant that is growing at the farthest point from your plant. All the devil's weed plants that are growing in between are yours. Later ... you can extend the size of your territory by following the watercourse form each point along the way." Music has always sent out lines of flight, like so many "transformational multiplicities," even overturning the very codes that structure or arborify it; that is why musical form, right down to its ruptures and proliferations, is comparable to a weed, a rhizome.

Write to the nth power, the n-1 power, write with slogans: Make rhizomes, not roots, never plant! Don't sow, grow offshoots! Don't be one or multiple, be multiplicities! Run lines, never plot a point! Speed turns the point into a line! Be quick, even when standing still! Line of chance, line of hips, line of flight. Don't bring out the General in you! Don't have just ideas, have just an idea (Godard). Have short-term ideas. Make maps, not photos or drawings. Be the Pink Panther and your loves will be like the wasp and the orchid, the cat and the baboon. As they say about old man river:

He don't plant 'tatos
Don't plant cotton
Them that plants them is soon forgotten
But old man river he just keeps rollin' along

A rhizome has no beginning or end; it is always in the middle, between things, interbeing, intermezzo.

...if we consider the plane of consistency we note that the most disparate of things and signs move upon it: a semiotic fragment rubs shoulders with a chemical interaction, an electron crashes into a language, a black hole captures a genetic message, a crystallization produces a passion, the wasp and the orchid cross a letter ... There is no "like" here, we are not saying "like an electron," "like an interaction," etc. The plane of consistency is the abolition of all metaphor; all that consists is Real. These are electrons in person, veritable black holes, actual organites, authentic sign sequences. It's just that they have been uprooted from their strata, destratified, decoded, deterritorialized, and that is what makes their proximity and interpenetration in the plane of consistency possible. A silent dance.

If evolution includes any veritable becomings, it is in the domain of symbioses that bring into play beings of totally different scales and kingdoms, with no possible filiation. There is a block of becoming that snaps up the wasp and the orchid, but from which no wasp-orchid can ever descend. There is a block of becoming that takes hold of the cat and baboon, the alliance between which is effected by a C virus. There is a block of becoming between young roots and certain microorganisms, the alliance between which is effected by the materials synthesized in the leaves (rhizosphere). If there is orginality in neoevolutionism, it is attributable in part to phenomena of this kind in which evolution does not go from something less differentiated to something more differentiated, in which it ceases to be a hereditary filiative evolution, becoming communicative or contagious. Accordingly, the term we would prefer for the form of evolution between heterogeneous terms is "involution," on the condition that involution is in no way confused with regression. Becoming is involutionary, involution is creative.

The line or block of becoming that unites the wasp and the orchid produces a shared deterritorialization: of the wasp, in that it becomes a liberated piece of the orchid's reproductive system, but also of the orchid, in that it becomes the object of an orgasm in the wasp, also liberated from its own reproduction. A coexistence of two asymmetrical movements that combine to form a block, down a line of flight that sweeps away selective pressures. The line, or the block, does not link the wasp to the orchid, any more than it conjugates or mixes them: it passes between them, carrying them away in a shared proximity in which the discernibility of points disappears. The line-system (or block-system) of becoming is opposed to the point-system of memory. Becoming is the movement by which the line frees itself from the point, and renders points indiscernible: the rihzome, the opposite of arborescence; break away from arborescence. Becoming is an antimemory.

How does actualization occur in things themselves? ... Beneath the actual qualities and extensities [of things themselves] there are spatio-temporal dynamisms. They must be surveyed in every domain, even though they are ordinarly hidden by the constituted qualities and extensities. Embryology shows that the division of the egg is secondary in relation to more significant morphogenetic movements: the augmentation of free surfaces, stretching of cellullar layers, invagination by folding, regional displacement of groups. A whole kinimatics of the egg appears which implies a dynamic. —Deleuze

Rhizosphere visualization :: The Rhizosphere is the zone surrounding the roots of plants in which complex relations exist among the plant, the soil microorganisms and the soil itself. The plant roots and the biofilm associated with them can profoundly, influence the chemistry of the soil including pH and nitrogen transformations. The fluorescence microscopic image [page top] shows red fluorescing fungal filaments across the rhizosphere of spring wheat together with mainly red fluorescent bacteria. The original image was at 100X and is a part of the ASM Biofilm Collection. This exercise developed by J.R. Heckman (Plant Science Department, Rutgers University, New Brunswick, NJ.) and J.E. Strick (Program in History of Science, Princeton University, Princeton, NJ. illustrates a technique by which the rhizosphere of plants can be visualized by its effect on soil pH.


Martin Day, PhD, Cardiff School of Biosciences :: Bacteria are ubiquitous microorganisms that can sometimes be cultured in isolation on selective media. My research interests are broad in the sense I have looked at gene exchange in Gram-positives and Gram-negatives, in clinical and ‘ecological’ sites. However the theme is really encompasssed by a desire to understand how genetic interactions (of gene flow and exchange) and selection drive microbial evolution. All bacteria participate in gene exchange and the three recognised mechanisms that have evolved are designed to do so. One of which is termed transduction. This process is driven by bacteriophage. When these phage plate on their host (Figure 1) they produce distinctive plaque morphologies. Of many questions you could ask, it is interesting to ask how and why three have evolved? Is any one more significant than any other?
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