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Darwin’s Big Idea May Be The Biggest Yet

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Back in 1859, Charles Darwin released his famous theory of evolution by natural selection whereby inherent variations in the individual members of some population of organisms under consideration would eventually lead to speciation events due to those variations producing a differential in survival and reproductive success and thus leading to the natural selection of some subset of organisms within that population.  As Darwin explained in his On The Origin of Species:

If during the long course of ages and under varying conditions of life, organic beings vary at all in the several parts of their organisation, and I think this cannot be disputed; if there be, owing to the high geometrical powers of increase of each species, at some age, season, or year, a severe struggle for life, and this certainly cannot be disputed; then, considering the infinite complexity of the relations of all organic beings to each other and to their conditions of existence, causing an infinite diversity in structure, constitution, and habits, to be advantageous to them, I think it would be a most extraordinary fact if no variation ever had occurred useful to each being’s own welfare, in the same way as so many variations have occurred useful to man. But if variations useful to any organic being do occur, assuredly individuals thus characterised will have the best chance of being preserved in the struggle for life; and from the strong principle of inheritance they will tend to produce offspring similarly characterised. This principle of preservation, I have called, for the sake of brevity, Natural Selection.

While Darwin’s big idea completely transformed biology in terms of it providing (for the first time in history) an incredibly robust explanation for the origin of the diversity of life on this planet, his idea has since inspired other theories pertaining to perhaps the three largest mysteries that humans have ever explored: the origin of life itself (not just the diversity of life after it had begun, which was the intended scope of Darwin’s theory), the origin of the universe (most notably, why the universe is the way it is and not some other way), and also the origin of consciousness.

Origin of Life

In order to solve the first mystery (the origin of life itself), geologists, biologists, and biochemists are searching for plausible models of abiogenesis, whereby the general scheme of these models would involve chemical reactions (pertaining to geology) that would have begun to incorporate certain kinds of energetically favorable organic chemistries such that organic, self-replicating molecules eventually resulted.  Now, where Darwin’s idea of natural selection comes into play with life’s origin is in regard to the origin and evolution of these self-replicating molecules.  First of all, in order for any molecule at all to build up in concentration requires a set of conditions such that the reaction leading to the production of the molecule in question is more favorable than the reverse reaction where the product transforms back into the initial starting materials.  If merely one chemical reaction (out of a countless number of reactions occurring on the early earth) led to a self-replicating product, this would increasingly favor the production of that product, and thus self-replicating molecules themselves would be naturally selected for.  Once one of them was produced, there would have been a cascade effect of exponential growth, at least up to the limit set by the availability of the starting materials and energy sources present.

Now if we assume that at least some subset of these self-replicating molecules (if not all of them) had an imperfect fidelity in the copying process (which is highly likely) and/or underwent even a slight change after replication by reacting with other neighboring molecules (also likely), this would provide them with a means of mutation.  Mutations would inevitably lead to some molecules becoming more effective self-replicators than others, and then evolution through natural selection would take off, eventually leading to modern RNA/DNA.  So not only does Darwin’s big idea account for the evolution of diversity of life on this planet, but the basic underlying principle of natural selection would also account for the origin of self-replicating molecules in the first place, and subsequently the origin of RNA and DNA.

Origin of the Universe

Another grand idea that is gaining heavy traction in cosmology is that of inflationary cosmology, where this theory posits that the early universe underwent a period of rapid expansion, and due to quantum mechanical fluctuations in the microscopically sized inflationary region, seed universes would have resulted with each one having slightly different properties, one of which that would have expanded to be the universe that we live in.  Inflationary cosmology is currently heavily supported because it has led to a number of predictions, many of which that have already been confirmed by observation (it explains many large-scale features of our universe such as its homogeneity, isotropy, flatness, and other features).  What I find most interesting with inflationary theory is that it predicts the existence of a multiverse, whereby we are but one of an extremely large number of other universes (predicted to be on the order of 10^500, if not an infinite number), with each one having slightly different constants and so forth.

Once again, Darwin’s big idea, when applied to inflationary cosmology, would lead to the conclusion that our universe is the way it is because it was naturally selected to be that way.  The fact that its constants are within a very narrow range such that matter can even form, would make perfect sense, because even if an infinite number of universes exist with different constants, we would only expect to find ourselves in one that has the constants within the necessary range in order for matter, let alone life to exist.  So any universe that harbors matter, let alone life, would be naturally selected for against all the other universes that didn’t have the right properties to do so, including for example, universes that had too high or too low of a cosmological constant (such as those that would have instantly collapsed into a Big Crunch or expanded into a heat death far too quickly for any matter or life to have formed), or even universes that didn’t have the proper strong nuclear force to hold atomic nuclei together, or any other number of combinations that wouldn’t work.  So any universe that contains intelligent life capable of even asking the question of their origins, must necessarily have its properties within the required range (often referred to as the anthropic principle).

After our universe formed, the same principle would also apply to each galaxy and each solar system within those galaxies, whereby because variations exist in each galaxy and within each substituent solar system (differential properties analogous to different genes in a gene pool), then only those that have an acceptable range of conditions are capable of harboring life.  With over 10^22 stars in the observable universe (an unfathomably large number), and billions of years to evolve different conditions within each solar system surrounding those many stars, it isn’t surprising that eventually the temperature and other conditions would be acceptable for liquid water and organic chemistries to occur in many of those solar systems.  Even if there was only one life permitting planet per galaxy (on average), that would add up to over 100 billion life permitting planets in the observable universe alone (with many orders of magnitude more life permitting planets in the non-observable universe).  So given enough time, and given some mechanism of variation (in this case, differences in star composition and dynamics), natural selection in a sense can also account for the evolution of some solar systems that do in fact have life permitting conditions in a universe such as our own.

Origin of Consciousness

The last significant mystery I’d like to discuss involves the origin of consciousness.  While there are many current theories pertaining to different aspects of consciousness, and while there has been much research performed in the neurosciences, cognitive sciences, psychology, etc., pertaining to how the brain works and how it correlates to various aspects of the mind and consciousness, the brain sciences (though neuroscience in particular) are in their relative infancy and so there are still many questions that haven’t been answered yet.  One promising theory that has already been shown to account for many aspects of consciousness is Gerald Edelman’s theory of neuronal group selection (NGS) otherwise known as neural Darwinism (ND), which is a large scale theory of brain function.  As one might expect from the name, the mechanism of natural selection is integral to this theory.  In ND, the basic idea consists of three parts as read on the Wiki:

  1. Anatomical connectivity in the brain occurs via selective mechanochemical events that take place epigenetically during development.  This creates a diverse primary neurological repertoire by differential reproduction.
  2. Once structural diversity is established anatomically, a second selective process occurs during postnatal behavioral experience through epigenetic modifications in the strength of synaptic connections between neuronal groups.  This creates a diverse secondary repertoire by differential amplification.
  3. Re-entrant signaling between neuronal groups allows for spatiotemporal continuity in response to real-world interactions.  Edelman argues that thalamocortical and corticocortical re-entrant signaling are critical to generating and maintaining conscious states in mammals.

In a nutshell, the basic differentiated structure of the brain that forms in early development is accomplished through cellular proliferation, migration, distribution, and branching processes that involve selection processes operating on random differences in the adhesion molecules that these processes use to bind one neuronal cell to another.  These crude selection processes result in a rough initial configuration that is for the most part fixed.  However, because there are a diverse number of sets of different hierarchical arrangements of neurons in various neuronal groups, there are bound to be functionally equivalent groups of neurons that are not equivalent in structure, but are all capable of responding to the same types of sensory input.  Because some of these groups should in theory be better than others at responding to some particular type of sensory stimuli, this creates a form of neuronal/synaptic competition in the brain, whereby those groups of neurons that happen to have the best synaptic efficiency for the stimuli in question are naturally selected over the others.  This in turn leads to an increased probability that the same network will respond to similar or identical signals in the future.  Each time this occurs, synaptic strengths increase in the most efficient networks for each particular type of stimuli, and this would account for a relatively quick level of neural plasticity in the brain.

The last aspect of the theory involves what Edelman called re-entrant signaling whereby a sampling of the stimuli from functionally different groups of neurons occurring at the same time leads to a form of self-organizing intelligence.  This would provide a means for explaining how we experience spatiotemporal consistency in our experience of sensory stimuli.  Basically, we would have functionally different parts of the brain, such as various maps in the visual centers that pertain to color versus others that pertain to orientation or shape, that would effectively amalgamate the two (previously segregated) regions such that they can function in parallel and thus correlate with one another producing an amalgamation of the two types of neural maps.  Once this re-entrant signaling is accomplished between higher order or higher complexity maps in the brain, such as those pertaining to value-dependent memory storage centers, language centers, and perhaps back to various sensory cortical regions, this would create an even richer level of synchronization, possibly leading to consciousness (according to the theory).  In all of the aspects of the theory, the natural selection of differentiated neuronal structures, synaptic connections and strengths and eventually that of larger re-entrant connections would be responsible for creating the parallel and correlated processes in the brain believed to be required for consciousness.  There’s been an increasing amount of support for this theory, and more evidence continues to accumulate in support of it.  In any case, it is a brilliant idea and one with a lot of promise in potentially explaining one of the most fundamental aspects of our existence.

Darwin’s Big Idea May Be the Biggest Yet

In my opinion, Darwin’s theory of evolution through natural selection was perhaps the most profound theory ever discovered.  I’d even say that it beats Einstein’s theory of Relativity because of its massive explanatory scope and carryover to other disciplines, such as cosmology, neuroscience, and even the immune system (see Edelman’s Nobel work on the immune system, where he showed how the immune system works through natural selection as well, as opposed to some type of re-programming/learning).  Based on the basic idea of natural selection, we have been able to provide a number of robust explanations pertaining to many aspects of why the universe is likely to be the way it is, how life likely began, how it evolved afterward, and it may possibly be the answer to how life eventually evolved brains capable of being conscious.  It is truly one of the most fascinating principles I’ve ever learned about and I’m honestly awe struck by its beauty, simplicity, and explanatory power.

DNA & Information: A Response to an Old ID Myth

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A common myth that goes around in Intelligent Design (creationist) circles is the idea that DNA can only degrade over time, and thus any and all mutations are claimed to be harmful and only serve to reduce “information” stored in that DNA.  The claim is specifically meant to suggest that evolution from a common ancestor is impossible by naturalistic processes because DNA wouldn’t have been able to form in the first place and/or it wouldn’t be able to grow or change to allow for speciation.  Thus, the claim implies that either an intelligent designer had to intervene and guide evolution every step of the way (by creating DNA, fixing mutations as they occurred or preventing them from happening, and then ceasing this intervention as soon as scientists began studying genetics), or it implies that all organisms must have been created all at once by an intelligent designer with DNA that was “intelligently” designed to fail and degrade over time (thus questioning the intelligence of this designer).

These claims have been refuted a number of times over the years by the scientific community with a consensus that’s been drawn from years of research in evolutionary biology among other disciplines, and the claims seem to be mostly a result of fundamental misunderstandings of biology (or intentional misrepresentations of the facts) and also the result of an improper application of information theory to biological processes.  What’s unfortunate is that these claims are still circulating around, largely because the propagators aren’t interested in reason, evidence, or anything that may threaten their beliefs in the supernatural, and so they simply repeat this non-sense to others without fact checking them and without any consideration as to whether the claims even appear to be rational or logically sound at all.

After having recently engaged in a discussion with a Christian that made this very claim (among many other unsubstantiated, faith-based assertions), I figured it would be useful to demonstrate why this claim is so easily refutable based on some simple thought experiments as well as some explanations and evidence found in the actual biological sciences.  First, let’s consider a strand of DNA with the following 12 nucleotide sequence (split into triplets for convenience):

ACT-GAC-TGA-CAG

If a random mutation occurs in this strand during replication, say, at the end of the strand, thus turning Guanine (G) to Adenine (A), then we’d have:

ACT-GAC-TGA-CAA

If another random mutation occurs in this string during replication, say, at the end of the string once again, thus turning Adenine (A) back to Guanine (G), then we’d have the original nucleotide sequence once again.  This shows how two random mutations could lead to the same original strand of genetic information, thus showing how it can lose its original information and have it re-created once again.  It’s also relevant to note that because there are 64 possible codons produced from the four available nucleotides (4^3 = 64), and since only 20 amino acids are needed to make proteins, there are actually several codons that code for any individual amino acid.

In the case given above, the complementary RNA sequence produced for the two sequences (before and after mutation) would be:

UGA-CUG-ACU-GUC (before mutation)
UGA-CUG-ACU-GUU (after mutation)

It turns out that GUC and GUU (the last triplets in these sequences) are both codons that code for the same amino acid (Valine), thus showing how a silent mutation can occur as well, where a silent mutation is one in which there are no changes to the amino acids or subsequent proteins that the sequence codes for (and thus no functional change in the organism at all).  The fact that silent mutations even exist also shows how mutations don’t necessarily result in a loss or change of information at all.  So in this case, as a result of the two mutations, the end result was no change in the information at all.  Had the two strands been different such that they actually coded for different proteins after the initial mutation, then the second mutation would have reversed this problem anyway thus re-creating the original information that was lost.  So this demonstration in itself already refutes the claim that DNA can only lose information over time, or that mutations necessarily lead to a loss of information.  All one needs are random mutations, and there will always be a chance that some information is lost and then re-created.  Furthermore, if we had started with a strand that didn’t code for any amino acid at all in the last triplet, and then the random mutation changed it such that it did code for an amino acid (such as Valine), this would be an increase in information regardless (since a new amino acid was expressed that was previously absent), although this depends on how we define information (more on that in a minute).

Now we could ask, is the mutation valuable, that is, conducive to the survival of the organism?  That would entirely depend on the internal/external environment of that organism.  If we changed the diet of the organism or the other conditions in which it lived, we could arrive at opposite conclusions.  Which goes to show that of the mutations that aren’t neutral (most mutations are neutral), those that are harmful or beneficial are often so because of the specific internal/external environment under consideration. If an organism is able to digest lactose exclusively and it undergoes a mutation that provides some novel ability of digesting sucrose at the expense of digesting lactose a little less effectively than before, this would be a harmful mutation if the organism lived in an environment with lactose as the only available sugar.  If however, the organism was already in an environment that had more sucrose than lactose available, then the mutation would obviously be beneficial for now the organism could exploit the most available food source.  This would likely lead to that mutation being naturally selected for and increasing its frequency in the gene pool of that organism’s local population.

Another thing that is often glossed over with the Intelligent Design (ID) claims about genetic information being lost is the fact that they first have to define what exactly information is necessarily before presenting the rest of their argument.  Whether or not information is gained or lost requires knowing how to measure information in the first place.  This is where other problems begin to surface with ID claims like these because they tend to leave this definition either poorly defined, ambiguous or conveniently malleable to serve the interests of their argument.  What we need is a clear and consistent definition of information, and then we need to check that the particular definition given is actually applicable to biological systems, and then we can check to see if the claim is true.  I have yet to see this actually demonstrated successfully.  I was able to avoid this problem in my example above, because no matter how information is defined, it was shown that two mutations can lead to the original nucleotide sequence (whatever amount of genetic “information” that may have been).  If the information had been lost, it was recreated, and if it wasn’t technically lost at all during the mutation, then it shows that not all mutations lead to a loss of information.

I would argue that a fairly useful and consistent way to define information in terms of its application to describing the evolving genetics of biological organisms would be to describe it as any positive correlation between the functionality that the genetic sequences code for and the attributes of the environment that the organism is contained in.  This is useful because it represents the relationship between the genes and the environment and it seems to fit in line with the most well-established models in evolutionary biology, including the fundamental concept of natural selection leading to favored genotypes.

If an organism has a genetic sequence such that it can digest lactose (as per my previous example), and it is within an environment that has a supply of lactose available, then whatever genes are responsible for that functionality are effectively a form of information that describes or represents some real aspects of the organism’s environment (sources of energy, chemical composition, etc.).  The more genes that do this, that is, the more complex and specific the correlation, the more information there is in the organism’s genome.  So for example, if we consider the aforementioned mutation that caused the organism to develop a novel ability to digest sucrose in addition to lactose, then if it is in an environment that has both lactose and sucrose, this genome has even more environmental information stored within it because of the increased correlation between that genome and the environment.  If the organism can most efficiently digest a certain proportion of lactose versus sucrose, then if this optimized proportion evolves to approach the actual proportion of sugars in the environment around that organism (e.g. 30% lactose, 70% sucrose), then once again we have an increase in the amount of environmental information contained within its genome due to the increase in specificity.

Defining information in this way allows us to measure degrees of how well-adapted a particular organism is (even if only one trait or attribute at a time) to its current environment as well as its past environment (based on what the convergent evidence suggests) and it also provides at least one way to measure how genetically complex the organism is.

So not only are the ID claims about genetic information easily refuted with the inherent nature of random mutations and natural selection, but we can also see that the claims are further refuted once we define genetic information such that it encompasses the fundamental relationship between genes and the environment they evolve in.

The Origin and Evolution of Life: Part II

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Even though life appears to be favorable in terms of the second law of thermodynamics (as explained in part one of this post), there have still been very important questions left unanswered regarding the origin of life including what mechanisms or platforms it could have used to get itself going initially.  This can be summarized by a “which came first, the chicken or the egg” dilemma, where biologists have wondered whether metabolism came first or if instead it was self-replicating molecules like RNA that came first.

On the one hand, some have argued that since metabolism is dependent on proteins and enzymes and the cell membrane itself, that it would require either RNA or DNA to code for those proteins needed for metabolism, thus implying that RNA or DNA would have to originate before metabolism could begin.  On the other hand, even the generation and replication of RNA or DNA requires a catalytic substrate of some kind and this is usually accomplished with proteins along with metabolic driving forces to accomplish those polymerization reactions, and this would seem to imply that metabolism along with some enzymes would be needed to drive the polymerization of RNA or DNA.  So biologists we’re left with quite a conundrum.  This was partially resolved when several decades ago, it was realized that RNA has the ability to not only act as a means of storing genetic information just like DNA, but it also has the additional ability of catalyzing chemical reactions just like an enzyme protein can.  Thus, it is feasible that RNA could act as both an information storage molecule as well as an enzyme.  While this helps to solve the problem if RNA began to self-replicate itself and evolve over time, the problem still remains of how the first molecules of RNA formed, because it seems that some kind of non-RNA metabolic catalyst would be needed to drive this initial polymerization.  Which brings us back to needing some kind of catalytic metabolism to drive these initial reactions.

These RNA polymerization reactions may have spontaneously formed on their own (or evolved from earlier self-replicating molecules that predated RNA), but the current models of how the early pre-biotic earth would have been around four billion years ago seem to suggest that there would have been too many destructive chemical reactions that would have suppressed the accumulation of any RNA and would have likely suppressed other self-replicating molecules as well.  What seems to be needed then is some kind of a catalyst that could create them quickly enough such that they would be able to accumulate in spite of any destructive reactions present, and/or some kind of physical barrier (like a cell wall) that protects the RNA or other self-replicating polymers so that they don’t interact with those destructive processes.

One possible solution to this puzzle that has been developing over the last several years involves alkaline hydrothermal vents.  We actually didn’t know that these kinds of vents existed until the year 2000 when they were discovered on a National Science Foundation expedition in the mid-Atlantic.  Then a few years later they were studied more closely to see what kinds of chemistries were involved with these kinds of vents.  Unlike the more well-known “black smoker” vents (which were discovered in the 1970’s), these alkaline hydrothermal vents have several properties that would have been hospitable to the emergence of life back during the Hadeon eon (between 4.6 and 4 billion years ago).

The ocean water during the Hadeon eon would have been much more acidic due to the higher concentrations of carbon dioxide (thus forming carbonic acid), and this acidic ocean water would have mixed with the hydrogen-rich alkaline water found within the vents, and this would have formed a natural proton gradient within the naturally formed pores of these rocks.  Also, electron transfer would have likely occurred when the hydrogen and methane-rich vent fluid contacted the carbon dioxide-rich ocean water, thus generating an electrical gradient.  This is already very intriguing because all living cells ultimately derive their metabolic driving forces from proton gradients or more generally from the flow of some kind of positive charge carrier and/or electrons.  Since the rock found in these vents undergoes a process called surpentization, which spreads the rock apart into various small channels and pockets, many different kinds of pores form in the rocks, and some of them would have been very thin-walled membranes separating the acidic ocean water from the alkaline hydrogen.  This would have facilitated the required semi-permeable barrier that modern cells have which we expect the earliest proto-cells to also have, and it would have provided the necessary source of energy to power various chemical reactions.

Additionally, these vents would have also provided a source of minerals (namely green rust and molybdenum) which likely would have behaved as enzymes, catalyzing reactions as various chemicals came into contact with them.  The green rust could have allowed the use of the proton gradient to generate molecules that contained phosphate, which could have stored the energy produced from the gradient — similar to how all living systems that we know of store their energy in ATP (Adenosine Tri-Phosphate).  The molybdenum on the other hand would have assisted in electron transfer through those membranes.

So this theory provides a very plausible way for catalytic metabolism as well as proto-cellular membrane formation to have resulted from natural geological processes.  These proto-cells would then likely have begun concentrating simple organic molecules formed from the reaction of CO2 and H2 with all the enzyme-like minerals that were present.  These molecules could then react with one another to polymerize and form larger and more complex molecules including eventually nucleotides and amino acids.  One promising clue that supports this theory is the fact that every living system on earth is known to share a common metabolic system, known as the citric acid cycle or Kreb’s cycle, where it operates in the forward direction for aerobic organisms and in the reverse direction for anaerobic organisms.  Since this cycle consists of only 11 molecules, and since all biological components and molecules that we know of in any species have been made by some number or combination of these 11 fundamental building blocks, scientists are trying to test (among other things) whether or not they can mimic these alkaline hydrothermal vent conditions along with the acidic ocean water that would have been present in the Hadrean era and see if it will precipitate some or all of these molecules.  If they can, it will show that this theory is more than plausible to account for the origin of life.

Once these basic organic molecules were generated, eventually proteins would have been able to form, some of which that could have made their way to the membrane surface of the pores and acted as pumps to direct the natural proton gradient to do useful work.  Once those proteins evolved further, it would have been possible and advantageous for the membranes to become less permeable so that the gradient could be highly focused on the pump channels on the membrane of these proto-cells.  The membrane could have begun to change into one made from lipids produced from the metabolic reactions, and we already know that lipids readily form micelles or small closed spherical structures once they aggregate in aqueous conditions.  As this occurred, the proto-cells would no longer have been trapped in the porous rock, but would have eventually been able to slowly migrate away from the vents altogether, eventually forming the phospholipid bi-layer cell membranes that we see in modern cells.  Once this got started, self-replicating molecules and the rest of the evolution of the cell would have underwent natural selection as per the Darwinian evolution that most of us are familiar with.

As per the earlier discussion regarding life serving as entropy engines and energy dissipation channels, this self-replication would have been favored thermodynamically as well because replicating those entropy engines and the energy dissipation channels means that they will only become more effective at doing so.  Thus, we can tie this all together, where natural geological processes would have allowed for the required metabolism to form, thus powering organic molecular synthesis and polymerization, and all of these processes serving to increase entropy and maximize energy dissipation.  All that was needed for this to initiate was a planet that had common minerals, water, and CO2, and the natural geological processes can do the rest of the work.  These kinds of planets actually seem to be fairly common in our galaxy, with estimates ranging in the billions, thus potentially harboring life (or where it is just a matter of time before it initiates and evolves if it hasn’t already).  While there is still a lot of work to be done to confirm the validity of these models and to try to find ways of testing them vigorously, we are getting relatively close to solving the puzzle of how life originated, why it is the way it is, and how we can better search for it in other parts of the universe.

The Origin and Evolution of Life: Part I

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In the past, various people have argued that life originating at all let alone evolving higher complexity over time was thermodynamically unfavorable due to the decrease in entropy involved with both circumstances, and thus it was believed to violate the second law of thermodynamics.  For those unfamiliar with the second law, it basically asserts that the amount of entropy (often referred to as disorder) in a closed system tends to increase over time, or to put it another way, the amount of energy available to do useful work in a closed system tends to decrease over time.  So it has been argued that since the origin of life and the evolution of life with greater complexity would entail decreases in entropy, these events are therefore either at best unfavorable (and therefore the result of highly improbable chance), or worse yet they are altogether impossible.

We’ve known for quite some time now that these thermodynamic arguments aren’t at all valid because earth isn’t a thermodynamically closed or isolated system due to the constant supply of energy we receive from the sun.  Because we get a constant supply of energy from the sun, and because the entropy increase from the sun far outweighs the decrease in entropy produced from all biological systems on earth, the net entropy of the entire system increases and thus fits right in line with the second law as we would expect.

However, even though the emergence and evolution of life on earth do not violate the second law and are thus physically possible, that still doesn’t show that they are probable processes.  What we need to know is how favorable the reactions are that are required for initiating and then sustaining these processes.  Several very important advancements have been made in abiogenesis over the last ten to fifteen years, with the collaboration of geologists and biochemists, and it appears that they are in fact not only possible but actually probable processes for a few reasons.

One reason is that the chemical reactions that living systems undergo produce a net entropy as well, despite the drop of entropy associated with every cell and/or it’s arrangement with respect to other cells.  This is because all living systems give off heat with every favorable chemical reaction that is constantly driving the metabolism and perpetuation of those living systems. This gain in entropy caused by heat loss more than compensates for the loss in entropy that results with the production and maintenance of all the biological components, whether lipids, sugars, nucleic acids or amino acids and more complex proteins.  Beyond this, as more complexity arises during the evolution of the cells and living systems, the entropy that those systems produce tends to increase even more and so living systems with a higher level of complexity appear to produce a greater net entropy (on average) than less complex living systems.  Furthermore, once photosynthetic organisms evolved in particular, any entropy (heat) that they give off in the form of radiation ends up being of lower energy (infrared) than the photons given off by the sun to power those reactions in the first place.  Thus, we can see that living systems effectively dissipate the incoming energy from the sun, and energy dissipation is energetically favorable.

Living systems seem to serve as a controllable channel of energy flow for that energy dissipation, just like lightning, the eye of a hurricane, or a tornado, where high energy states in the form of charge gradients or pressure or temperature gradients end up falling to a lower energy state by dissipating that energy through specific focused channels that spontaneously form (e.g. individual concentrated lightning bolts, the eye of a hurricane, vortices, etc.).  These channels for energy flow are favorable and form because they allow the energy to be dissipated faster since the channels are initiated by some direction of energy flow that is able to self-amplify into a path of decreasing resistance for that energy dissipation.  Life and the metabolic processes involved with it, seem to direct energy flow in ways that are very similar to these other naturally arising processes in non-living physical systems.  Interestingly enough, a relevant hypothesis has been proposed for why consciousness and eventually self-awareness would have evolved (beyond the traditional reasons proposed by natural selection).  If an organism can evolve the ability to predict where energy is going to flow, where an energy dissipation channel will form (or form more effective ones themselves), conscious organisms can then behave in ways that much more effectively dissipate energy even faster (and also by catalyzing more entropy production), thus showing why certain forms of biological complexity such as consciousness, memory, etc., would have also been favored from a thermodynamic perspective.

Thus, the origin of life as well as the evolution of biological complexity appears to be increasingly favored by the second law, thus showing a possible fundamental physical driving force behind the origin and evolution of life.  Basically, the origin and evolution of life appear to be effectively entropy engines and catalytic energy dissipation channels, and these engines and channels produce entropy at a greater rate than the planet otherwise would in the absence of that life, thus showing at least one possible driving force behind life, namely, the second law of thermodynamics.  So ironically, not only does the origin and evolution of life not violate the second law of thermodynamics, but it actually seems to be an inevitable (or at least favorable) result because of the second law.  Some of these concepts are still being developed in various theories and require further testing to better validate them but they are in fact supported by well-established physics and by consistent and sound mathematical models.

Perhaps the most poetic concept I’ve recognized with these findings is that life is effectively speeding up the heat death of the universe.  That is, the second law of thermodynamics suggests that the universe will eventually lose all of its useful energy when all the stars burn out and all matter eventually spreads out and decays into lower and lower energy photons, and thus the universe is destined to undergo a heat death.  Life, because it is producing entropy faster than the universe otherwise would in the absence of that life, is actually speeding up this inevitable death of the universe, which is quite fascinating when you think about it.  At the very least, it should give a new perspective to those that ask the question “what is the meaning or purpose of life?”  Even if we don’t think it is proper to think of life as having any kind of objective purpose in the universe, what life is in fact doing is accelerating the death of not only itself, but of the universe as a whole.  Personally, this further reinforces the idea that we should all ascribe our own meaning and purpose to our lives, because we should be enjoying the finite amount of time that we have, not only as individuals, but as a part of the entire collective life that exists in our universe.

To read about the newest and most promising discoveries that may explain how life got started in the first place, read part two here.