Founding day, May 1, found us on line. Informal discussion with the faculty (ff's) senate, by that evening offered oriented vibrations toward developing a personality within this new institution. It will attempt rigor and good humor. Of the two possible forms of expression, comedic or tragic and dramatic, we opt for the former.
This is your AM (ancient mariner) call. We present a 'brief' paragraph of some additional introduction to our university and its style-to-be. Many of you may recall the toy, a small round box with a playing field of small holes and a ball. The object of the play is to keep the ball rolling, by jiggling the box, so that it circles around the pitfalls. We are going to try to keep you moving and circling around our themes in the style of play of 'Bourbaki'. Punch and Judy, and an American TV sitcom. A few of our auditors have caught on, in part, to the need of looking up words we use in a 'good' dictionary or encyclopedia to feel for the sense of the discourse we conduct. Why is this needed? Very simple.
Language is a very entangling web. It is loaded with meaning. It almost requires a thick book of unpacking for each word. That, in part, is the dilemma we face in an exposition of homeokinetics (as a physics for complex systems). Read our recent article on language in Winter 1977, Comparative Civilizations Review for a taste of the problem of communication - with self or others. Enough. Since we want to get on to two great antinomies: is there a physical science for the biological system without vitalistic undertones; is there a physical science for the human social system with 'explanatory' and 'predictive' power, we have to keep moving. [We can express our basic issue as: is you is, is you ain't.; or in higher class form,"to be or not to be" without metaphor]
Our physically oriented group in the social sciences - nine disciplines in all - gave a seminar series to an applied school of technical study [occupational therapy, at USC] in 1992. The following handout was used as what appeared to be a useful introduction to homeokinetics. As such, it may serve, once again, to stimulate multidisciplined dialogues with other systems' outlooks. If you are prepared to enter into discussion, feel free to either attack or defend the theses (or both). If adequately sharp, it will be presented (Fax or call (714) 768 1963).
Complex Systems Science (Homeokinetics): Principles and Applications (Seminar 1/31/93)
The sum of momentum-displacement product interactions is measured by a small number of units of a fundamental 'natural' constant of action, Planck's constant h.
Our macroscopic form of that principle is that an energy dissipating complex field unit expends a unit of factory day action which is characteristic of the complex atomistic species (note that according to the first law of thermodynamics, energy in the physical universe is neither created nor destroyed; but according to the second law it may be transformed dissipatively into lower, more degraded forms of energy). We have scaled that measure H for all mammals. It varies with the 0.80 power of adult body mass; illustratively, about 2,000 kcal-days of action per day for humans.
What is proposed is to maintain a single species colony of say 10,000 live bacteria in a particular region in a flow system. Take a U-tube and arrange a steady drip of water into that tube so that it overflows out in the exit end, say at a level a little lower than at the entrance end. By changing the difference in height, we can adjust to any velocity flow field that we wish to elect. Our proposal is to maintain a colony of bacteria in the entrance region of the tube at a definite number level. However, we propose to make them work at some reachable energy consumption level within their competence. That is why we have adjusted the velocity of the field. We propose to make them swim at that speed.
The external modes of action of flagellated bacteria are: ingest food, swim in a straight line by rotating their flagella one preferred way, and tumble in motion by reversing that flagellar motion. The empirical findings are that in favorable media, the straight line segments are longer. The resultant motion is an apparent diffusion up a favorable food gradient. In addition, there is a division period in which the bacteria divide in half (double their number) by reproductive fission. That time scale depends on temperature. A common temperature range is somewhere between near freezing and boiling water temperatures. A typical doubling time at room temperature may be in the vicinity of, say, 20 minutes. Thus one elects some in-between temperature to thermostat the flow system.
Now we have to know the energy consumption of our selected bacterial species when swimming in a stream of our elected velocity at our given temperature. We can perform tests on a small sample to determine that specific consumption, or we might make a crude estimate from our mammalian data. Such an estimate might come out in the vicinity of say 50 picograms (10-12 grams) per minute of glucose. So we add such a stream of glucose to our U-tube flow system.
What would happen if we put in one, a few, the number we wish to maintain, or many more of our desired bacteria? Obviously they would be swept along by the stream, but in the competition for the limited glucose supply, (a) there would be continued growth and division, number doubling per 20 minutes, and (b) by glucose depletion, there would form a gradient of glucose concentration in the stream, so that the more favorable region of occupancy is toward the entrance. A diminishing exponential concentration would develop, concentrating the cell number up near the entrance. Is that the flow equilibrium resultant?
No, because the energy expenditure is for the dissipative cost of swimming. It does not supply the required material - proteins and nucleic acids - needed to maintain the bacterial body material growth supply. Thus the doubling growth could not take place. Either the number growth would have to stop, or - if forced to continue - some cells would become moribund and die. Since they could not swim, they would be swept away.
Thus we see the additional conservation condition. To maintain a dilute noninteracting colony of say 10,000 bacteria, we have to supply the material replacement for the bacteria that die and are swept away. So we must add to our stream the required material flux in protein or amino acids and nucleic acids that are disappearing. If the various streams are correct in magnitude, then when we introduce whatever number of the pure strain we wish to maintain, it will move by fission and death toward the equilibrium in number, in action, in mass flow streams, and in the energy stream that represents one point in the equation of state for those bacteria at that operating temperature, with no unaccounted-for ingredients in the outflow. By repeating the experiment at different temperatures and velocities, etc., we can determine the entire mathematical relationship among the components of this four variable equation of state (This is as an idealized but realizable equation of state. There are some more dynamic unstable states for the bacterial processes which are possible, but we do not have to confront them in our first simple modelling). And then this can be done for other living species. Social systems for modern humans can be similarly treated with some further extension. [To be done in the future].