08.18.08

Where Does Probability Come From? (and randomness to boot)

Posted in Idependence Friendly logic, Relativity, Special Relativity, biology, epistemology, evolution, fitness, fun, logic, measurement, mind, philosophy, physics, science, technology at 1:26 pm by nogre


I just returned from a cruise to Alaska. It is a wonderful, beautiful place. I zip-lined in a rain forest canopy, hiked above a glacier, kayaked coastal Canada and was pulled by sled-dogs. Anywho, as on many cruises, there was a casino, which is an excellent excuse for me to discuss probability.

What is probability and where does it come from? Definitions are easy enough to find. Google returns:

a measure of how likely it is that some event will occur; a number expressing the ratio of favorable cases to the whole number of cases possible …

So it’s a measure of likelihood. What’s likelihood? Google returns:

The probability of a specified outcome.

Awesome. So ‘probability as likelihood’ is non-explanatory. What about this ‘ratio of favorable cases to the whole number of cases possible’? I’m pretty wary about the word favorable. Let’s modify this definition to read:

a number expressing the ratio of certain cases to the whole number of cases possible.

Nor do I like ‘a number expressing…’ This refers to a particular probability, not probability at large, so let’s go back to using ‘measure’:

a measure of certain cases to the whole number of cases possible.

We need to be a bit more explicit about what we are measuring:

a measure of the frequency of certain cases to the whole number of cases possible.

OK. I think this isn’t that bad. When we flip a fair coin the probability is the frequency of landing on heads compared to the total cases possible, heads + tails, so 1 out of 2. Pretty good.

But notice the addition of the word fair. Where did it come from, what’s it doing there? Something is said to be fair if that thing shows no favoritism to any person or process. In terms of things that act randomly, this means that the thing acts in a consistently random way. Being consistently random means it is always random, not sometimes random and other times not random. This means that fairness has to do with the distribution of the instances of the cases we are studying. What governs this distribution?

In the case of of a coin, the shape of the coin and the conditions under which it is measured make all the difference in the distribution of heads and tails. The two sides, heads and tails, must be distinguishable, but the coin must be flipped in a way such that no one can know which side will land facing up. The shape of the coin, even with uniform mass distribution, cannot preclude this previous condition. Therefore the source of probability is the interdependence of physical conditions (shape and motion of the coin) and an epistemic notion (independence of knowledge of which side will land up). When the physical conditions and our knowledge of the conditions are dependent upon each other then the situation becomes probabilistic because the conditions preclude our knowing the exact outcome of the situation.

It is now time to recall that people cheat at gambling all the time. A trio of people in March 2004 used a computer and lasers to successfully predict the decaying orbit of a ball spinning on a roulette wheel (and walked out with £1.3 million). This indicates that after a certain point it is possible to predict the outcome of a coin flipping or a roulette ball spinning, so the dependence mentioned above is eventually broken. However this is only possible once the coin is flipping or the roulette ball is rolling, not before the person releases the roulette ball or flips the coin.

With the suggestion that it is the person that determines the outcome we can expand the physical-epistemic dependence to an physical-epistemic-performative one. If I know that I, nor anyone else, can predict the outcome until after I perform a task, then the knowledge of the outcome is dependent upon how I perform that task.

This makes sense because magicians and scam artists train themselves to be able to perform tasks like shuffling and dealing cards in ways that most of us think is random but are not. The rest of us believe that there is a dependence between the physical setup and the outcome that precludes knowing the results, but this is merely an illusion that is exploited.

What about instances in which special training or equipment is unavailable; can we guarantee everyone’s ability to measure the thing in question to be equal? We can: light. Anyone who can see at all sees light that is indistinguishable from the light everyone else sees: it has no haecceity.

This lack of distinguishability, lack of haecceity (thisness), is not merely a property of the photon but a physical characteristic of humans. We have no biology that can distinguish one photon from another of equivalent wavelength. To distinguish something we have to use a smaller feature of the thing to tell it apart from its compatriots. Since we cannot see anything smaller, this is impossible. Nor is there a technology that we could use to augment our abilities: for us to have a technology that would see something smaller than a photon would require us to know that the technology interacted at a deeper level with reality than photons do. But we cannot know that because we are physically limited to using the photon as our minimal measurement device. The act of sight is foundational: we cannot see anything smaller than a photon nor can anything smaller exist in our world.

The way we perceive photons will always be inherently distributed because of this too. We cannot uniquely identify a single photon, and hence we can’t come back and measure the properties of a photon we have previously studied. Therefore the best we will be able to accomplish when studying photons is to measure a group of photons and use a distribution of their properties, making photons inherently probabilistic. Since the act of seeing light is a biological feature of humans, we all have equal epistemological footing in this instance. This means that the epistemic dependence mentioned above can be ignored because it adds nothing to the current discussion. Therefore we can eliminate the epistemic notion from our above dependence, reducing it to a physical-performative interdependence.

Since it is a historical/ evolutionary accident that the photon is the smallest object we can perceive, the photon really is not fundamental to this discussion. Therefore, the interdependence of the physical properties of the smallest things we can perceive and our inherent inability to tell them apart is a source of probability in nature.

This is a source of natural randomness as well: once we know the probability of some property that we cannot measure directly, the lack of haecceity means that we will not be able to predict when we will measure an individual with said property. Therefore the order in which we measure the property will inherently be random. [Assume the contradiction: the order in which we measure the property is not random, but follows some pattern. Then there exists some underlying structure that governs the appearance of the property. However, since we are already at the limit of what can be measured, no such thing can exist. Hence the order in which we measure the property is random.]

————–

If I were Wittgenstein I might have said:

Consider a situation in which someone asks, “How much light could you see?” Perhaps a detective is asking a hostage about where he was held. But then the answer is, “I didn’t look.” —— And this would make no sense.

hmmmm…. I did really mean to get back to gambling.

 


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03.18.08

Psychopharmacological Enhancement

Posted in biology, ethics, evolution, fitness, mind, philosophy, technology at 9:47 pm by nogre


The only ways to enhance the mind is to learn or evolve. Since evolution is out of our hands, all that is left is to learn.

Drugs that purport psychopharmacological enhancement do not do what their name states: they may change certain psychological factors but there is no drug that will make you smarter. This would be to eat from the tree of knowledge.

However drugs may be able to let you do things that you were unable previously, but this is nothing mysterious. If you do not breath enough oxygen, you will not be able to run. You get enough oxygen, you will be able to do more things. Now is oxygen a performance enhancing drug? It depends: the World Anti-Doping Agency recently ruled on oxygen tents (tents that vary the amount of oxygen inside) because using these tents can affect red blood cell counts. This example illustrates two things: that there is nothing inherently special about any particular chemical, be it oxygen or a newfangled drug, and secondly, that drugs only affect intermediary situations, not the final outcome.

The first point is that there is no moral dimension associated with the chemicals themselves. If it is possible to use the most fundamental of chemicals required for our survival in a way that could be seen as inappropriate, then any other chemical could be equally accused. If any chemical can be equally accused, then there is nothing unique about any individual chemical that makes its use morally wrong.

The second point is that drugs only have a specific range of effects. In the above example, the oxygen tents affect red blood cell count. An increased red blood cell count can be used to boost endurance, but this benefit will only appear under certain situations. The tents themselves do not increase endurance: they merely increase red blood cells. If a different drug was consumed to weaken the muscles, then the two ‘drugs’ would counteract each other and there would be no change in ability. Therefore it is not a drug that gives people an ability, such as endurance, but a drug may change how an ability is expressed.

The question is (and always was), “What do you want?” Since drugs have no moral dimension nor imbue the user with unknown (super-human) ability, the only issue is of fair play. Fair play in terms of other people and with your own goals. If you want to be able to lift heavy things, then you can use a machine, you can use drugs or you can work hard. Using a machine or drugs is to use someone else’s technology to assist whatever ability you have. If you use discipline to achieve the same results, then the technology that is being used is your own. Therefore if you are trying to play fair with others, then you have to ensure everyone has access to the same technology, be it machine or drug. If you are trying to achieve something yourself, then only you know whether or not using drugs makes a difference.

As we learn what is safe(r), we are going to have a fun future. Nothing changes our natural born ability or the hard work we have put in, but that has never stopped us from trying. Better drugs are on the way and this means options will be open to us that weren’t possible in the past. Good luck, be safe, have fun.

 


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12.05.07

The Logic of Biological Relativity [draft]

Posted in Idependence Friendly logic, Relativity, biology, evolution, fitness, game theory, logic, measurement, science at 7:57 pm by nogre


How can we represent biological relativity in logical notation?

Organism a is adapting relative to organism b

Aab

Organism b is adapting relative to a

Aba

Organisms a and b are adapting relative to each other

Aab & Aba

This schema is unsatisfactory because it describes the situation from an indeterminate outside perspective: a and b are said to be adapting relative to each other without regard to the observer describing the situation. Relativity applies to all the perspectives in question (with special focus on any observer perspective) and hence we need a way to include the observer perspective. This means we need to take into account how the observer is adapted such that the observer(s) can be compared to the organisms in question.

To remedy this problem let quantifiers range over organisms and include witnesses to identify the specific organisms in question:

For any organism x, for any organism y, there exists an organism z and there exists an organism u such that x is adapted relative to y according to organism z, and y is adapted relative to x according to organism u.

(∀x)(∀y)(∃z)(∃u)A[xyzu]

Unfortunately this formulation is insufficient because witness z is logically dependent upon both x and y (as is u as well) and we want z to only witness x and u to only witness y: as both z and u are dependent upon both x and y, both x and y must be chosen before selecting z and u. This means that organisms x and y are selected (logically) independent of the witness organisms defeating the purpose of having those witnesses.

Getting around this difficulty is not trivial in first order logic. There is no way in first order logic to linearly order the four quantifiers such that z only depends on x and u only depends on y (Kolak & Symons p.249 [p.40 of the pdf]). Independence Friendly logic suffices though :

(∀x)(∀y)(∃z/∀y)(∃u/∀x)A[xyzu]

This statement says that for any organism x, for any organism y, there exists an organism z that does not depend on y and an organism u that does not depend on x, such that organism x as witnessed by z, and organism y as witnessed by u, are adapted relative to each other.

However, though this statement gets very close to describing biological relativity, if we consider how the witnesses witness the organisms, i.e. how z witnesses the organism x, there is a problem. By stating that z witnesses x and that z is independent of y, the statement ‘x is adapted relative to y as witnessed by z’ is nonsense: since z is independent of y it could not be a witness to ‘x adapting relative to y.’ Likewise for u.

The solution is simple enough though:

(∀x)(∀y)(∃z/∀x)(∃u/∀y)((x=z) & (y=u) & A[x,y])

By letting x=z, making z independent of x and dependent on y, z witnesses y from the perspective of x without requiring x to be chosen before z. Likewise for u: if y=u, u is logically independent of y and u is dependent on x, then u may be chosen before y, u is dependent as a witness to the choice of x and witnesses x from the perspective of y. Perhaps more prosaically: x and y are adapting relative to each other, as witnessed by organisms z and u (who have the equivalent adaptations respectively to x and y), and it is not necessary to predetermine what those adaptations are.

 


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12.04.07

Relativity in Biology notes from 2005

Posted in General Relativity, Relativity, Special Relativity, biology, evolution, fitness, measurement, philosophy, physics, science at 8:22 pm by nogre


It’s always interesting to see the start of ideas. Although I don’t have anything from the Spring of ‘04 when I recall realizing biorelativity for the first time, I have found a file with a ‘last modified’ date of June12, ‘05, the contents of which are below:

Quantum Biology

biology: the study of the physical attributes of life.

the rate of mutation is constant, much as the speed of light

organisms mutate. light shines. hence organisms bend/curve life-time as objects bend/curve space-time. greater the mass, the more the curve… the greater the inertia (momentum), the greater the curve. so what is meant by inertia in biology (or in physics)? what does mutation light, as photons light objects? [mutation is the smallest unit of life. photons smallest things with momentum.] we use mutation to view changes of a species. so if a species remains the same, its genetic(?) inertia/ momentum is remaining constant. that with the greatest inertia/ momentum creates the most gravity. that with the greatest inertia/ momentum creates biological gravitation towards itself…

space as vacuum for objects, DNA as vacuum for mutations. objects bend space; mutations do what to DNA? organisms bend life. as objects move to the speed of light their mass (apparently) goes to infinity. as organisms move to the rate of mutation (sex), their DNA (apparently) goes to infinity. as objects slow to absolute 0, their mass (apparently) disappears; as organisms cease mutation (death) the DNA (apparently) disappears. [space is a non-material object, same as concepts, numbers, words etc]

so when there is some massive change to the organism.. say when bats developed sonar, every other mutation became pulled closer around that as to become a part of it. nose, ears, face… eyes are just satellites now

we can then use the fossil history to see what was a major mutative innovation of the day- when preexisting mutations became reoriented around a new mutation (as we can see objects by the change they cause in the motion of other objects, and know their relative size)

location * momentum </= const
species * mutation </= const

——————-

Biological General, Special and plain Relativity in both physics and biology are all confused and mixed together and I was nowhere near my current understanding of biological mass (which didn’t happen till sometime in September of this year and perhaps I’ll go through how I came to that a bit later). It looks like I used DNA for biological mass.

Still, there is a lot of good stuff here.

 


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11.17.07

Why Evolutionary Principles Cannot be Used to Support Racial Prejudices DRAFT

Posted in biology, evolution, fitness, measurement, news, philosophy, science at 3:40 pm by nogre


Evolutionary principles are sometimes used to justify racial prejudices. While no rigorous scientific study has yet proven one race to be inferior to any others it should be recognized that it is in principle impossible to prove racial superiority/inferiority and hence no study ever will.

Firstly a note on the meaning of ‘more evolved’ and ‘less evolved’. Every species on the face of the earth today has been evolving for the exact same amount of time. We all started at the same time. However you believe that life started, either as a single celled organism in the ancient seas of earth or by some intervention, if you believe in evolution then everything started roughly at that one point and proceeded from there. Hence we are all equally evolved, from humans to gnats. The only things that may be considered less evolved are things that are no longer around to complain about it.

Secondly, if the claim of racial superiority/inferiority is not one of being ‘more evolved’, then it is a claim about being differently evolved to have some properties that other races do not have. This roughly means that one race has some qualities that make them more fit, or, conversely, one race lacks some features that the rest of us have (even if they have made it this far) that makes them less fit. Either way the claim boils down to either having or lacking a certain characteristic or characteristics. These characteristics, by definition, were passed down through the successive generations eventually proliferating throughout a family, later a population and thence to the entire race some time later.

In order to objectively measure the fitness of an organism or species we need to be able to replicate a controlled environment and a control group. Regardless of the implications of cloning people for a control group, the concept of a controlled human environment will present us with insurmountable theoretical problems.

The environment that we place organisms in is the ‘test’ that we are judging them on. Specifically, if we want to see which of two species flourishes in a particular environment we would place both in the same environment and see what happens. However, not only is it impossible for us to replicate an environment to test people in, none of us know what the future will hold for our species. Hence, without foresight into the future, it is impossible for us to have an environment that could be used as an objective test environment.

In lieu of this impossible situation, approximations are the only possibility. To approximate requires making decisions about what will be included and what will be excluded. The decisions made will influence the results making them a function of the decisions made. Hence it is impossible to approximate without biasing the results, rendering the study useless for the purpose of establishing superiority.

Since we are all here now and none of us knows the future, there will be no study that can prove the superiority or inferiority of any race. Anyone who claims otherwise is claiming they can predict the future perfectly, is racist or both.

——-

If there are any argument structure fans (such as myself woohoo!) this argument’s in a mathematical induction style. The first paragraph argues against a base case (of a race being no more fit than any other) and then the subsequent paragraphs argue against any possible way to argue that the property (of being no more fit) could be used as an inductive hypothesis: Base case is day zero for our species, in which we are all obviously equally fit, and then the induction is on day n (today) and n+1 (tomorrow). Since we are all here now and none of us know what tomorrow holds (by way of Relativity in Evolutionary Biology we have no way objectively view the trajectory of our species), we can move from n to n+1 and the inductive step is made. Hence it is impossible to prove future fitness in our species.

If anyone cares to give me some feedback, I’d like to know if you think it is worthwhile to include some of this argument structure stuff into the body of the paper. I’ve had experiences where I’ve written arguments but people have completely missed them because they were not as familiar with argument forms.

Also would it be worth it to have some commentary on recent developments such as Watson’s gaff or the recent NYTimes article about genetics and race?

 


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11.13.07

Evolutionary Drift, revisited yet again

Posted in General Relativity, Relativity, biology, evolution, fitness, measurement, philosophy, physics, science at 9:32 pm by nogre


With my recent paper on Measuring Fitness I realize that my previous responses to evolutionary drift, though not incorrect, may have not stated the solution particularly clearly. When fitness is defined and measured as described in the aforementioned article, evolutionary drift is irrelevant. The method of measuring the fitness of an organism or species makes no reference to any mutations whatsoever. Therefore evolutionary drift is no problem for the theory of fitness described here.

If we are trying to identify whether a certain mutation makes an organism more fit, we can of course test it against an organism without that mutation. However if we are unable to test it (say we are studying a historical period or it is just unfeasible), then I believe my previous posts are accurate. I mainly argue that you can’t tell what exactly makes an organism more fit- it’s an underdetermination thesis of sorts - based upon our limited evolutionary perspective.

I think I just failed to say how irrelevant drift was to fitness before this.

 


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11.12.07

Measuring Fitness

Posted in General Relativity, Relativity, biology, evolution, fitness, measurement, philosophy, physics, science at 12:01 am by nogre


The basic premise is to measure fitness in a conceptually similar way to how we measure mass.  To measure mass we can use a scale to compare the effect of gravity on a test object to an object with an agreed upon mass, or we can compare the test object’s resistance to acceleration as compared to an object with an agreed upon mass.  These methods measure the ‘gravitational’ mass and ‘inertial mass’ respectively.

Gravitational Mass and Selection Fitness

Measuring an object’s gravitational mass requires a uniform gravitational field, e.g. the gravitational field at the surface of the earth.  The gravitational field accelerates things based upon how massive they are: the more massive an object is the greater the force that the gravitational field exerts.  To measure the mass of an object it is placed on one pan of a scale and pre-calibrated masses (objects of known mass) are placed on the other pan.  When the two pans are level the test object has an equivalent mass to the calibrated masses because they have equivalent forces being applied to them by the gravitational field.

To measure fitness we require a similar experimental setup.  First, a uniform gravitational field: according to the General Theory of Biological Relativity ecosystems create large natural selection fields.  A uniform natural selection field requires an ecosystem free from disturbances which could skew the reproductive rates of the organisms.  Secondly we would need organisms with a standard fitness.  A suitable organism would be easily clonable and of a fitness that we suspect our test organism to be near.  That organism’s fitness would be defined as one ‘biogram’ (or what you will).  Lastly we would need to see how the organisms fair in the ecosystem.  Their fitness will be proportional: if both proliferate (or die off) at the same rate, then their fitness will be equivalent, if one does much better than the other then it’s fitness will be proportionally higher.

Inertial Mass and Survival Fitness

Measuring an object’s inertial mass is measuring how resistant it is to acceleration as compared to how resistant to acceleration an object of known mass is.  To measure inertial mass the test mass is attached to a spring clamped horizontally to a stable structure.  The mass and spring are then pulled to one side and let oscillate back and forth: the more massive the object, the slower oscillations.  The number of oscillations per unit of time can be compared to the oscillations per time of a known mass and thence the inertial mass can be calculated.

As above a controlled environment and an organism whose fitness is known (even if by definition) is needed.  However the organisms need to be ‘accelerated’ for this measurement.  According to the General Theory of Biological Relativity environmental conditions will dictate how a species changes over time.  Therefore to ‘accelerate’ a species a changing environment is needed.  Simply put: measuring ‘survival fitness’ is measuring how well an organism or species fairs in a changing environment.  For example a plant that can survive in a wide range of temperatures will be fitter than one that requires a narrow temperature range.  If a test plant proliferates and the benchmark organism withers under a temperature swing, the test organism has a greater fitness.

 


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11.05.07

NEWS: General Relativity in Evolutionary Biology Final Version and NYC Area Philosophy Mailing List started!!!!!

Posted in General Relativity, Relativity, Special Relativity, biology, evolution, fitness, internet, philosophy, physics, science at 5:33 pm by nogre


I’ve posted my final version of General Relativity in Evolutionary Biology to the articles section (and to GroundReport) and I’ve also started a mailing list/rss for philosophy events in NYC. So lots to check out.

 


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10.22.07

Blogged by The Philosophers’ Carnival #55, Sweet!

Posted in Relativity, fitness, internet, philosophy, science at 3:42 pm by nogre


The Philosopher’s Carnival picked up my Relativity in Evolutionary Biology! Completely cool. And I won the shortest description contest- take that all you people who write things that can be summarized. And hyphenation to boot. Props to the editor who used an archaic device to help me out in lieu of delving into unruly philosophy of science sure to scare people.

It’s all relative
Noah Greenstein has written a well-worth-a-peek post on ‘Relativity in Evolutionary Biology’ here.

 


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10.19.07

General Relativity in Evolutionary Biology DRAFT

Posted in General Relativity, Relativity, Special Relativity, biology, fitness, philosophy, physics, science at 3:37 pm by nogre


DRAFT: DO NOT REFERENCE/QUOTE THIS WORK WITHOUT MY EXPLICIT PERMISSION- Noah Greenstein

 
I’ve discussed relativity in evolutionary biology with regards to uniform change but, as with the Special Theory of Relativity in physics, we want a theory that covers all change.

This means that insofar as relativity applies to biology under uniform motion, i.e. when a species is reproducing in a regular fashion, we want a theory of relativity that applies to biology even when a species is undergoing non-uniform motion, i.e. when the species reproductive cycle has undergone a serious change. 

 

It is a fundamental equivalence of evolutionary biology that the struggle for survival and natural selection yield the exact same results.  This relationship has yet to be interpreted.  If we consider a person in love, financially secure and who wants nothing more than to raise children for foreseeable rest of his life.  That person may view this situation as the culmination of his struggle to survive and replicate.  That person may equally view the situation to be nature selecting him as suitable to continue life. 

 

For what apparently are good reasons action at a distance is not allowed.  Struggle for survival does not occur at a distance; ‘struggle’ seems to inherently imply some local interaction.  Natural selection, however, is much more amorphous in nature: how exactly does nature select?  I suggest that we think of natural selection as a biofield that acts upon organisms. 

 

 

Inertial ‘fitness’ and Gravitational ‘fitness’

 

 

The fitness of a thing creates a (teeny) natural selection field.  The fitness of a species creates a (small) natural selection field.  The fitness of an ecosystem creates a (large) natural selection field. 

 


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