#23. Proxy Natural Selection: The God-shaped Gap at the Heart of Biology [genetics, evolution]

EV    GE    

Red, theory; black, fact.

2-06-2017

As promised, here is my detailed and hypothetical description of the entity responsible for compensating for the fact that our microbial, insect, and rodent competitors evolve much faster than we do because of their shorter generation times. In these pages, I have been variously calling this entity the intermind, the collective unconscious, the mover of the zeitgeist, and the real, investigable system that the word "God" points to. I here recant my former belief that epigenetic marks are likely to be the basis of an information storage system sufficient to support an independent evolution-like process. I will assume that the new system, "proxy natural selection" (PNS) is DNA-based.

11-20-2017

The acronym PNS is liable to be confused with "peripheral nervous system," so a better acronym would be "PGS," meaning "post-zygotic gamete selection."

2-06-2017

First, a refresher on how standard natural selection works. DNA undergoes point mutations (I will deal with the other main type of mutation later) that add diversity to the genome. The developmental process translates the various genotypes into a somewhat diverse set of phenotypes. Existential selection then ensues from the interaction of these phenotypes with the environment, made chronically stringent by population pressure. Differential reproduction of phenotypes then occurs, leading to changes in gene frequencies in the population gene pool. Such changes are the essence of evolution.

PNS assumes that the genome contains special if-then rules, perhaps implemented as cis-control-element/structural gene partnerships, that collectively simulate the presence of an objective function that dictates the desiderata of survival and replaces or stands in for existential selection. A given objective function is species-specific but has a generic resemblance across the species of a genus. The genus-averaged objective function evolves by species-replacement group selection, and can thus theoretically produce altruism between individuals. The if-then rules instruct the wiring of the hypothalamus during development, which thereby comes to dictate the organism's likes and dislikes in a way leading to species survival as well as (usually) individual survival. Routinely, however, some specific individuals end up sacrificed for the benefit of the species.

Here is how PNS may work. Crossing-over mutations during meiosis to produce sperm increase the diversity of the recombinotypes making up the sperm population. During subsequent fertilization and brain development, each recombinotype instructs a particular behavioral temperament, or idiosyncratotype. Temperament is assumed to be a set of if-then rules connecting certain experiences with the triggering of specific emotions. An emotion is a high-level, but in some ways stereotyped, motor command, the details of which are to be fleshed out during conscious planning before anything emerges as overt behavior. Each idiosyncratotype interacts with the environment and the result is proxy-evaluated by the hypothalamus to produce a proxy-fitness (p-fitness) measurement. The measurement is translated into blood-borne factors that travel from the brain to the gonads where they activate cell-surface receptors on the spermatogonia. Good p-fitness results in the recombination hot spots of the spermatogonia being stabilized, whereas poor p-fitness results in their further destabilization. 

Thus, good p-fitness leads to good penetrance of the paternal recombinotype into viable sperm, whereas poor p-fitness leads to poor penetrance, because of many further crossing-over events. Changes in hotspot activity could possibly be due to changes in cytosine methylation status. The result is within-lifetime changes in idiosyncratotype frequencies in the population, leading to changes in the gross behavior of the population in a way that favors species survival in the face of environmental fluctuations on an oligogenerational timescale. On such a timescale, neither standard natural selection nor synapse-based learning systems are serviceable.

2-07-2017

The female version of crossing over may set up a slow, random process of recombination that works in the background to gradually erase any improbable statistical distribution of recombinotypes that is not being actively maintained by PNS.

7-29-2017

Here is a better theory of female PNS. First, we need a definition. PNS focus: a function that is the target of most PNS. Thus, in trees, the PNS focus is bio elaboration of natural pesticides. In human males, the PNS focus is brain development and the broad outlines of emotional reactivity, and thus behavior. In human females, the PNS focus is the digestive process. The effectiveness of the latter could be evaluated while the female fetus is still in the womb, when the eggs are developing. The proxy fitness measure would be how well nourished the fetus is, which requires no sensory experience. This explains the developmental timing difference between oogenesis and spermatogenesis. Digestion would be fine tuned by the females for whatever types of food happen to be available in a given time and place.

8-18-2017

Experimental evidence for my proposed recombination mechanism of proxy natural selection has been available since 2011, as follows:

Stress-induced recombination and the mechanism of evolvability

by Weihao Zhong; Nicholas K. Priest

Behavioral Ecology and Sociobiology, 03/2011, Volume 65, Issue 3

permalink:

http://ncsu.summon.serialssolutions.com/#!/search?bookMark=ePnHCXMwfV1NS8QwEC2yBz9-gxL0JgTytUl7EUQU767nkDQJeCgu7uLv903SVlEQepx0pmky8yaTvJx3G-StuZsLiKLydSpLO8QEx8Ry3J3QgR9Nmx6t2tAivxGcaNhOFw9qZd-fdXcv9bQER26Kr0yMMsQJ6WK1mCHPZoBIbMp0QvbtMLH3wjKm9GfjtwbEen163D088_lSAT4i9js-xgi_DdSQBplcwQhXIQSggNjHVEpwUlIlK-uSyJI4JMRspZKKymyzTfqiu27vXVy3n__6wQO9GARIQVXsqyZEbt7TWDl-hNEj1wHg2A5EOiqbwBIM_b6xS_iVR7h2mxcNpTtPN7vf_NIcIq2HjEeotopifT_8L_XDwNsmtZR_V_2ECDxpxqOr6m9j_wpDiOrp_r6N82bqPhW0uWxt6i7PtYGRhgh9lP4C2uagLw

Abstract:

"The concept of evolvability is controversial. To some, it is simply a measure of the standing genetic variation in a population and can be captured by the narrow-sense heritability (h2). To others, evolvability refers to the capacity to generate heritable phenotypic variation. Many scientists, including Darwin, have argued that environmental variation can generate heritable phenotypic variation. However, their theories have been difficult to test.

 Recent theory on the evolution of sex and recombination provides a much simpler framework for evaluating evolvability. It shows that modifiers of recombination can increase in prevalence whenever low fitness individuals produce proportionately more recombinant offspring. Because recombination can generate heritable variation, stress-induced recombination might be a plausible mechanism of evolvability if populations exhibit a negative relationship between fitness and recombination. Here we use the fruit fly, Drosophila melanogaster, to test for this relationship.

We exposed females to mating stress, heat shock or cold shock and measured the temporary changes that occurred in reproductive output and the rate of chromosomal recombination. We found that each stress treatment increased the rate of recombination and that heat shock, but not mating stress or cold shock, generated a negative relationship between reproductive output and recombination rate. The negative relationship was absent in the low-stress controls, which suggests that fitness and recombination may only be associated under stressful conditions. Taken together, these findings suggest that stress-induced recombination might be a mechanism of evolvability."

However, my theory also has a macro aspect, namely that the definition of what constitutes "stress," in terms of neuron interconnections or chemical signaling pathways, itself  evolves, by species-replacement group selection. Support for that idea is the next thing I must search for in the literature. &&

#22. The Cogs of Armageddon [evolutionary psychology]

EP

Red, theory; black, fact.

1-27-2017

This is a "just-so story" about how I believe everyday human behavior eventually accomplishes the all-important biological function of dispersal for the human race. A future post will attempt to explain how the "just-so story" got written in terms of natural selection and possible faster-acting proxies thereof needed by organisms with long generation times.

Dispersal is things like dandelions shedding airborne seeds, slime molds developing into spore cases on stalks and releasing the spores into the wind, territorial systems of birds and mammals forcing the unlanded young to seek widely for their own territories, and humans going into space because our science fiction writers keep scaring us about the possibility of meteor crashes wiping out life on Earth. To paraphrase the latter, a way to avoid extinction, long-term, is not putting all your eggs in one basket, geographically speaking.

The slime mold dictyostelium is triggered into its dispersal program by the food supply running short; I will adopt the assumption that the human dispersal program is also triggered by the end of the good times, that is, the price of bread rising relative to wages.

I conjecture that human neural pathways potentiate aggression when the hard times come, but of an elaborate kind adapted for ensuring efficient dispersal (i.e., with minimal loss of life). It begins with a two-person feud of the sort illustrated in cultural references too numerous to mention. In Canada, where I live, a cough accompanied by an angry expression plays the role of the instigation. The arbitrary stimulus, made offensive by some piece of Pavlovian conditioning, is traded back and forth with rapidly increasing energy. The process is remarkably like flirting, not surprising since the ultimate purpose has commonalities with reproduction--but of an entire society. 

However, the emotional component is strongly threatening rather than rewarding, because the participants must be induced to seek allies, which people do when threatened, until all of society is eventually polarized. The acts of provocation being traded back and forth become progressively more outrageous, as they must, to keep the polarization process going. Eventually, one side gets the upper hand and forces the other to flee.

The result is a diaspora, i.e., dispersal. Because of the long polarization process, an entire group is expelled, not single individuals one at a time. Thus, members of such a group can assist each other to survive and relocate, thereby reducing the mortality associated with dispersal, thereby making the dispersal event more efficient in terms of number of people relocated. The group who flees is then seen by the international community as the blameless victim, and the group who stays is seen as the unprincipled aggressor. This tends to elicit a sheltering of the refugees and an intimidation of the "aggressor," who is deterred from pressing his advantage, that is, pursuing the refugees and slaughtering them to the last man, which is what each side would dearly like to do to the other by this point. This, again, is an efficiency from the point of view of producing dispersal.

However, if each side is continually threatening the other, why don't they flee each other's presence during the very early stages? The answer seems to be that humans have a reflex that converts feeling threatened into a wish to injure the threatening party, possibly a behavioral leftover from some earlier adaptation, such as an anti-predation defense; to injure, you have to stick around. (Leftovers such as these form the building blocks of future just-so plots.)

Finally, settled refugees usually do not integrate completely into the host society, instead forming ethnic neighborhoods. This increases the resemblance to an entire society reproducing itself. However, the growth phase following reproduction in individuals seems to be lacking at the society level. However, being seen as ethnic by the host society, due to slow integration, could improve individual-level reproductive success of refugees because of disassortative mate-choice effects evolved to favor genes that produce dispersal.

2-24-2017

The dispersal-producing dynamic just outlined is fantastically powerful, as it must be to overcome all the reasons you would not leave your homeland forever at some arbitrary time: expense, risk of mortality in transit, opportunity costs, temporary loss of livelihood, need to learn a new language and customs, vulnerability to exploitation in the new country, etc., etc.

This dynamic is basically what theologians call evil, for which I propose the less judgmental, substitute term "dispersalism." If this is truly an insight, it should have a liberating effect on your life, even if you just remember that one word, but with the price of always being population-conscious: always trying to see what is happening at the population/zeitgeist level, and reading the paper every day at the very least.

At least one "just-so story" could probably be written for each of the pillars of the human species-specific objective function mentioned in previous posts, these being as follows: dispersal, genetic diversity, memetic diversity, and altruism. (The latter has not been mentioned until now.) Each of these must be optimized, not blindly maximized, for each comes at a cost. In terms of neurobiology, each pillar is probably a family of functionally related likes and dislikes wired up in the hypothalamus, but not obviously related to individual-level survival or reproduction.

#21. Is Higher Math Really Undiscovered Physics? [physics]

PH

Red, theory; black, fact.

This post was inspired by the realization that to progress in physics, we need to accept the Newtonian position that absolute space exists. Not only that, but that it is complicated, like a network, crystal, or condensate. Too many fundamental constants of nature (20, according to Lee Smolin) are required to explain the behaviour of supposedly elementary particles with no internal structures to which such constants could refer.

Thus, the constants must refer to the vacuum between the particles, now more readily understood as a complex medium. Looking at the pattern set by the rest of physics and cosmology, such a medium is more readily understood as a condensate of myriad "space-forming entities." Matter would be flaws in this condensate, entropy left over from its rapid formation. Energy may have the same relation to time: irregularities in its rate of progression.

To theorize about how space formed and what came before it, we have to give up visualization, obviously. I suspect this will be a big deal for most physicists. However, the abstractions of higher math may be an island of understanding already existing on the far side of the spatial thought barrier.

In other words, sets, integers, categories, mappings, etc., may be concrete things, and not abstractions at all. Presumably, our spatial and temporal reality still bears the properties it had from the very earliest stages of the universe, co-existing with later-developed properties, which have enabled mathematicians throughout history to access the deepest levels of description of reality, deeper than space time itself.

Consider set theory. Can the familiar concepts of set, union, intersection, and complement be placed into correspondence with physical processes and objects in today's space time to make a case that set theory is pre-spatial physics, so primordial as to be literally unimaginable if thought of as the rules of a real universe? To get started, we have to begin with Leibniz's monads, the "empty set," now considered a real thing. (If you must visualize these, visualize something ridiculous like Cheereos™ floating in milk, when the bowl has reached the single-layer stage.)

The physical process of binding is prefigured by the set-theoretical operation of union. In the simplest case, two monads combine to form a second-order set.

The physical process of pattern recognition, which is, in essence, energy release, is prefigured by intersection. Note that with intersection, the internal subset structure of the set is important, suggesting that the "operating system" of the universe at this stage must keep track of such structures.

We can associate a size measure with a set, namely the total of all the monads inside it once all subsets have been accounted for. The usefulness of numbers in dealing with the world is explained if this size measure is the basis of laws governing what sets may combine as unions and in what frequency (i.e., fraction of all sets extant.)

The fact that most of physics seems to be governed by differential equations may be prefigured by a tendency of these combining laws to depend on the difference of two sizes. The set-theoretical operation of complementation may prefigure the existence of positive and negative charge and the Pauli exclusion principle of fermions, on which molecular complementarity interactions depend.

#20. The Two-clock Universe [physics]

PH

Red, theory; black, fact.

The arrow of time is thought to be thermodynamic in origin, namely the direction in which entropy (disorder of an isolated system) increases. Entropy is one of the two main extensive variables of thermodynamics, the other being volume. I would like to propose that since we live in an expanding universe, the direction of cosmological volume increase makes sense as a second arrow of time; it's just not our arrow of time.

One of the outstanding problems of cosmology is the nature of dark energy, thought to be responsible for the recently discovered acceleration of the Hubble expansion. Another problem is the nature of the inflationary era that occurred just after the Big Bang (BB), introduced to explain why the distribution of matter in the universe is smoother than predicted by the original version of the BB.

Suppose that the entropy of the universe slowly oscillates between a maximal value and a minimal value, like a mass oscillating up and down on the end of a spring, whereas the volume of the universe always smoothly increases. Thus, entropy would trace out a sinusoidal wave when plotted against volume.

If the speed of light is only constant against the entropic clock, then the cosmological acceleration is explainable as an illusion due to the slowing of the entropic increase that occurs when nearing the top of the entropy oscillation, just before it reverses and starts down again. The cosmological volume increase will look faster when measured by a slower clock.

The immensely rapid cosmological expansion imputed to the inflationary era would originate analogously, as an illusion caused by the slowness of the entropy oscillation when it is near the bottom of its cycle, just after having started upward again.

These ideas imply that entropy at the cosmological scale has properties analogous to those of a mass-and-spring system, namely inertia (ability to store energy in movement) and stiffness (ability to store energy in fields). The only place it could get these properties appears to be from the subatomic particles of the universe and their fields. Thus, there has to be a hidden network of relationships among all the particles in the universe to create and maintain this correspondence. Is this the meaning of quantum-mechanical entanglement and quantum-mechanical conservation of information? However, if the universe is closed, properties of the whole universe, such as a long circumnavigation time at the speed of light, could produce the bounce.

These ideas also imply the apocalyptic conclusion that all structures in the present universe will be disassembled in the next half-period of the entropy oscillation. The detailed mechanism of this may be an endothermic, resonant absorption of infrared and microwave photons that have circumnavigated a closed universe and returned to their starting point. Enormous amounts of phase information would have to be preserved in intergalactic space for billions of years to make this happen, and here is where I depend heavily on quantum mechanical results. I have not figured out how to factor in the redshift due to volume expansion.&&

#19. Explaining Science-religion Antipathy also Explains Religion [evolutionary psychology]

EP

Red, theory; black, fact.

I will be arguing here that the Darwinian selective advantage to humans of having a propensity for religion is that it regulates the pace of introduction of new technology, which is necessitated by the disruptive side effects of new technology.

If this sounds like a weak argument, perhaps people have been chronically underestimating the costs to society of the harmful side effects of new technology, ever since there have been people. Take the downside of the taming of fire, for instance. You can bet that the first use would have been military, just as in the case of nuclear energy. Remember that everything was covered in forests in those days; there must have been an appalling time of fire until kin selection slowly put a stop to it. The lake-bottom charcoal deposits will still be there, if anyone cares to look for them. (Shades of Asimov's story "Nightfall.")

The sedimentary record does not seem to support the idea that the smoke from such a time of fire caused a planetary cooling event sufficient to trigger the last ice age. However, the mere possibility helps to drive home the point, namely that prehistoric, evolutionary-milieu technology was not necessarily too feckless to produce enough disruption to constitute a source of selection pressure.

Natural selection could have built a rate-of-innovation controller by exaggerating people's pleasure at discovering a new, unexplored phenomenon, until they bog down in rapture at that moment and never progress to the next step of actually experimenting or exploring. The latter activities would be just upstream of the nominally controlled process, the introduction of new technology. People's tendency for "rapture capture" would be causally linked via genetically specified neural pathways to the kinds of hardships caused by technological side effects, thereby completing a negative feedback loop that would work like a steam engine governor.

I conjecture that all present-day religions are built on this phenomenon of "rapture capture." This may explain why the most innovative country, the USA, is also the most religiose, according to Dawkins, writing in "The God Delusion." An Einsteinian sense of wonder at the cosmos that, according to Dawkins, most scientists feel, could be a mild, non-capturing version of the same thing. The unlikely traits attributed to God, omnipotence, omni this and that, could have instrumental value in intensifying the rapture.

Another possible name for what I have been calling rapture could be "arcanaphilia." A basic insight for me here was that religion is fundamentally hedonistic. I do not seem to be straying too far from Marx's statement that "Religion is the opiate of the people."

These ideas help to explain why some sciences such as astronomy and chemistry began as inefficient protosciences (e.g., astrology, alchemy): they were inhibited from the start by an excessive sense of wonder, until harder heads eventually prevailed (Galileo, Lavoisier). Seen as a protoscience, the Abrahamic religions could originally have been sparked by evidence that "someone is looking out for us" found in records of historical events such as those the ancient Israelites compiled (of which the Dead Sea Scrolls are a surviving example). That "someone" would in reality be various forms of generation-time compensation, one of which I have been calling the "intermind" in these pages. Perhaps when the subject of study is in reality a powerful aspect of ourselves as populations, the stimulus for rapture capture will be especially effective, explaining why religion has yet to become an experimental science.

By the way, there is usually no insurmountable difficulty in experimenting on humans so long as the provisions of the Declaration of Helsinki are observed: volunteer basis only; controlled, randomized, double-blind study; experiment thoroughly explained to volunteers before enrollment; written consent obtained from all volunteers before enrollment; approval of the experimental design obtained in advance from the appropriate institutional ethics committee; and the experiment registered online with the appropriate registry.

Religions seem to be characterized by an unmistakable style made up of little touches that exaggerate the practitioner's sense of wonder and mystery, thus, their arcanaphilic "high." I refer to unnecessarily high ceilings in places of worship, use of enigmatic symbols, putting gold leaf on things, songs with Italian phrases in the score, such as "maestoso," wearing colorful costumes, etc. I shall refer to all the elements of this style collectively as "bractea," Latin for tinsel or gold leaf. I propose the presence of bractea as a field mark for recognizing religions in the wild. By this criterion, psychiatry is not a religion, but science fiction is.

It seems to me that bractea use can easily graduate into the creation of formal works of art, such as canticles, stained glass windows, statues of the Buddha, and the covers of science fiction magazines. Exposure to concentrations of excessive creativity in places of worship can be expected to drive down the creativity of the worshipers by a negative feedback process evolved to regulate the diversity of the species memeplex, already alluded to in my post titled, "The Intermind: Engine of History?"

This effect should indirectly reduce the rate of introduction of new technology, thereby feeding into the biological mission of religion. Religion could be the epi-evolutionary solution, and the artistic feedback could be the evolutionary solution, to the disorders caused by creativity. Bractea would represent a synergy between the two.

#17. Hell's Kitchen [evolutionary psychology]

EP

Red, theory; black, fact.

Ever since the assassination of JFK in '63, people of my generation have been wondering why the Americans kill off their best and brightest. It's not just the Americans, of course. The same thing happened to Gandhi and Our Savior no less.

I think a homey kitchen metaphor nails it. Once you have emptied the milk carton of all its milk, you can use it to dispose of the grease. That is, by the logic of "The Insurance of the Heart," once tremendous acclaim has been conferred on someone's name, the physical person no longer matters for the purposes of enhancing the name their descendents will inherit, and so can safely be used to draw the fire of the genetic undesirables; the resulting tremendous indignation will confer bad odor on the name of said undesirable for quite long enough to eradicate their meh genes in all copies.

Thus, Booth's genes were eradicated to make way for Lincoln's, and Oswald's genes were eradicated to make way for Kennedy's, without overall change in population density.

If the intermind could be said to have thoughts, this is what they would be like. Clearly, it's not God.

#16. The Intermind, Engine of History? [evolutionary psychology]

EP

Red, theory; black, fact.

9-21-2016

This post is a further development of the ideas in the post, "What is intelligence? DNA as knowledge base." It was originally published 9-21-2016 and extensively edited 10-09-2016 with references added 10-11-2016 and 10-30-2016. Last modified: 10-30-2016.

In "AviApics 101" and "The Insurance of the Heart," I seem to be venturing into human sociobiology, which one early critic called "An outbreak of neatness." With the momentum left over from "Insurance," I felt up for a complete human sociobiological theory, to be created from the two posts mentioned.

However, what I wrote about the "genetic intelligence" suggests that this intelligence constructs our sociobiology in an ad hoc fashion, by rearranging a knowledge base, or construction kit, of "rules of conduct" into algorithm-like assemblages. This rearrangement is (See Deprecated, Part 7) blindingly fast by the standards of classical Darwinian evolution, which only provides the construction kit itself, and presumably some further, special rules equivalent to a definition of an objective function to be optimized. The ordinary rules translate experiences into the priming of certain emotions, not the emotions themselves, 

Thus, my two sociobiological posts are best read as case studies of the products of the genetic intelligence. I have named this part the intermind, because it is intermediate in speed between classical evolution and learning by operant conditioning. (All three depend on trial-and error.) The name is also appropriate in that the intermind is a distributed intelligence, acting over continental, or a least national, areas. If we want neatness, we must focus on its objective function, which is simply whatever produces survival. It will be explicitly encoded into the genes specifying the intermind, (For more on multi-tier, biological control systems with division of labor according to time scale, see "Sociobiology: the New Synthesis," E. O. Wilson, 1975 & 2000, chapter 7.)

Let us assume that the intermind accounts for evil, and that this is because it is only concerned with survival of the entire species and not with the welfare of individuals. Therefore, it will have been created by group selection of species. (Higher taxonomic units such as genus or family will scarcely evolve because the units that must die out to permit this are unlikely to do so, because they comprise relatively great genetic and geographical diversity.* However, we can expect adaptations that facilitate speciation. Imprinted genes may be one such adaptation, which might enforce species barriers by a lock-and-key mechanism that kills the embryo if any imprinted gene is present in either two or zero active copies.) Species group selection need act only on the objective function used by epigenetic trial-and-error processes.

In these Oncelerian times, we know very well that species survival is imperiled by loss of range and by loss of genetic diversity. Thus, the objective function will tend to produce range expansion and optimization of genetic diversity. My post "The Insurance of the Heart" concluded with a discussion of "preventative evolution," which was all about increasing genetic diversity. My post "AviApics 101" was all about placing population density under a rigid, negative feedback control, which would force excess population to migrate to less-populated areas, thereby expanding range. Here we see how my case studies support the existence of an intermind with an objective  function as described above.

However, all this is insufficient to explain the tremendous cultural creativity of humans, starting at the end of the last ice age with cave paintings, followed shortly thereafter by the momentous invention of agriculture. The hardships of the ice age must have selected genes for a third, novel component, or pillar, of the species objective function, namely optimization of memetic diversity. Controlled diversification of the species memeplex may have been the starting point for cultural creativity and the invention of all kinds of aids to survival. Art forms may represent the sensor of a feedback servomechanism by which a society measures its own memeplex diversity, measurement being necessary to control.

A plausible reason for evolving an intermind is that it permits larger body size, which leads to more internal degrees of freedom and therefore access to previously impossible adaptations. For example, eukaryotes can phagocytose their food; prokaryotes cannot. However, larger body size comes at the expense of longer generation time, which reduces evolvability. A band of high frequencies in the spectrum of environmental fluctuations therefore develops where the large organism has relinquished evolvability, opening it to being out competed by its smaller rivals. 

The intermind is a proxy for classical evolution that fills the gap, but it needs an objective function to provide it with its ultimate gold standard of goodness of adaptations. Species-replacement group selection makes sure the objective function is close to optimal. This group selection process takes place at enormously lower frequencies than those the intermind is adapting to, because if the timescales were  too similar, chaos would result. For example, in model predictive control, the model is updated on a much longer cycle than are the predictions derived from it.

12-25-2016

Today, when I was checking to see if I was using the word "cathexis" correctly (I wasn't), I discovered the Freudian term "collective unconscious," which sounds close to my "intermind" concept.

* 3-12-2018

I now question this argument. Why can't there be as many kinds of group selection as taxonomic levels? Admittedly, the higher-level processes would be mind-boggling in their slowness, but in evolution, there are no deadlines.