It looks like you're using an Ad Blocker.
Please white-list or disable AboveTopSecret.com in your ad-blocking tool.
Thank you.
Some features of ATS will be disabled while you continue to use an ad-blocker.
No, that's not all I've said. The point I'm trying to help you understand is that the organism represents an emergent property of the ecological relations it has with it's environment.
It means that when the environment changes significantly, the organism's thermodynamic structure either a) adapts by countering the effect of the environment, or b) dies off.
Sometimes, the organism becomes simpler in its organization, whereas other times the organism becomes more complex.Thus, evolution from prokaryotes to eukaryotes to sponge onward is a process of dynamic equilibrium with the environment, and, as the process continues, fusions and symbioses occur between cells, leading to a complexification of the total system i.e more elements, and indeed, symbioses like this entail a sort of "emegent property", where large-scale features of the environment (mechanics in movement, for instance) 'act down' upon the organization of the smallest elements.
I mentioned Terrence Deacon because you would do well to understand the concept of orthograde and contragrade, which helps explain how evolution could progress through non-stop oscillation between stability and organized chaos. An orthograde state corresponds to an attractor (a stable condition or a "structural coupling" with the environment) whereas a perturbation triggers a contragrade state, which, at this point, experiments with different adaptations to the pertubation to maintain its systems continuity. It's in contragrade states that growth and increased coherency can occur - what the ecologist Robert Ulanowicz calls "ascendance".
Also, and for someone who calls himself "seresnt of the lamb", it would be nice if you could be more mindful in your choice of words about what I mean i.e. "Are you just trying to use words you think most people won't take that time to look up?". This isn't an appropriate way of speaking - at least in real intellectual conversations, this would be regarded as an 'ad hominem' attack. Its also cynical and assumes that I am not making sense.
No, what makes sense - and what you should understand, is the diachronic nature of existence. You are obviously committed to a biblical timetable formulated in a period of human history where narrative and story-telling took the place of empirical study.
To know the mighty works of God; to comprehend His wisdom and majesty and power; to appreciate, in degree, the wonderful working of His laws, surely all this must be a pleasing and acceptable mode of worship to the Most High, to whom ignorance can not be more grateful than knowledge. --Copernicus
Those who study the stars have God for a teacher. -- Tycho Brahe
I do not feel obliged to believe that the same God who has endowed us with sense, reason, and intellect has intended us to forgo their use. --Galileo Galilei
When I reflect on so many profoundly marvelous things that persons have grasped, sought, and done, I recognize even more clearly that human intelligence is a work of God, and one of the most excellent. --Galileo Galilei
Our piety is deeper, the greater is our awareness of creation and its grandeur. --Johannes Kepler
We astronomers are priests of the highest God in regard to the book of nature. --Johannes Kepler
Thus I see plainly that the certainty and truth of all knowledge [scientiae] depends uniquely on my awareness of the true God, to such an extent that I was incapable of perfect knowledge [perfecte scire] about anything else until I became aware of him. -- Rene Decartes
There are two kinds of people one can call reasonable: those who serve God with all their heart because they know him, and those who seek him with all their heart because they do not know him. --Blaise Pascal
"The vastness, beauty, orderliness of heavenly bodies; the excellent structure of animals and plants; and other phenomena of nature justly induce an intelligent, unprejudiced observer to conclude a supreme, powerful, just, and good author." --Robert Boyle
Do you pay attention to your emotions when you write? This is another mean-spirited thing to say. I understand you - I'm not an idiot. You don't need to call the other person stupid if it you - in fact, who is having the problem understanding the nature of the criticism I'm making.
Buddy - I've already answered this. When you scale back billions of years ago into the precambrian you have nothing but different versions of life. You are assuming that life only happened once. I am assuming that the life we see today is the life that survived.
Now, you seem to think that invertebrates HAD to be the ancestor for modern vertebrates. THAT IS NOT NECESSARY. You are completely overlooking how unnecessary that assumption is - but clearly this is where your focus lies. As I've already written - and to which you felt the need to ignore and then mock - invertebrates may be the evolutionary heir to a DIFFERENT EUKARYOTIC ANCESTOR. This is your issue - I've explained it, have told you that this is not that big a problem, but you apparently see it as the death of the evolutionary theory.
My resolution: there were different sorts of bacteria with different genetic organizations of their nucleic acids. To say this is impossible is apparently gainsaid by the reality that vertebrates and invertebrates process oxygen in different ways. This merely means that the mitochondria - or ancient bacteria - had different ways of adapting to the presence of oxygen.
AGA and AGG were thought to have become mitochondrial stop codons early in vertebrate evolution (Osawa, Ohama, Jukes & Watanabe 1989). However, at least in humans it has now been shown that AGA and AGG sequences are not recognized as termination codons. A -1 mitoribosome frameshift occurs at the AGA and AGG codons predicted to terminate the CO1 and ND6 ORFs, and consequently both ORFs terminate in the standard UAG codon (Temperley et al. 2010).
Several arthropods translate the codon AGG as lysine instead of serine (as in the invertebrate mitochondrial genetic code) or arginine (as in the standard genetic code) (Abascal et al., 2006).
GUG may possibly function as an initiator in Drosophila (Clary and Wolstenholme, 1985; Gadaleta et al., 1988). AUU is not used as an initiator in Mytilus (Hoffmann et al., 1992).
Imaginary transitional invertabrets
originally posted by: ServantOfTheLamb
a reply to: Astrocyte
This is a plausible hypothesis but I feel it is at odds with observation. Let us again consider the car engine as thermodynamic system. You may be able to add, modify, or even remove entire constraints on that system and make it work better, but it is also just as reasonable to conclude that you may add, modify. or remove a constraint that is detrimental to the performance of the system. The latter seems to be more probable if the orthograde change in the environment that does the work for the contragrade change inside the organism is not controlled. The hierarchical nature of the dGRN makes certain constraints a necessity for the production of a new self-regulating system. So again I don't see how this helps one bypass the canalization of this system. Seems to be yet another problem for body plan morphogenesis.
Also, and for someone who calls himself "seresnt of the lamb", it would be nice if you could be more mindful in your choice of words about what I mean i.e. "Are you just trying to use words you think most people won't take that time to look up?". This isn't an appropriate way of speaking - at least in real intellectual conversations, this would be regarded as an 'ad hominem' attack. Its also cynical and assumes that I am not making sense.
Well 'ad hominem' would be me saying your argument is wrong, because of some flaw in your character. I never did that.At no point in time did I say you weren't making sense. The last post had no substance for me to respond to. It was just extremely general so since I don't know you personally this seems to be a perfectly reasonable question to ask, however since it offended you I will say I am sorry.
No, what makes sense - and what you should understand, is the diachronic nature of existence. You are obviously committed to a biblical timetable formulated in a period of human history where narrative and story-telling took the place of empirical study.
Please elaborate on what you mean by diachronic nature of existence. The statement is to general. Diachronic simply means concerned with the way in which something, especially language, has developed and evolved through time. So you are just saying I should understand that as things exist they develop and evolve thru time. I never denied that. I just think there are obviously limitations on what can happen when we study population genetics and the developmental biology. The reason empirical study took off was because theist in the 16th and 17th century wanted to read the book nature, which they thought gave you knowledge of God and was even a form of worship to them.
To know the mighty works of God; to comprehend His wisdom and majesty and power; to appreciate, in degree, the wonderful working of His laws, surely all this must be a pleasing and acceptable mode of worship to the Most High, to whom ignorance can not be more grateful than knowledge. --Copernicus
Those who study the stars have God for a teacher. -- Tycho Brahe
I do not feel obliged to believe that the same God who has endowed us with sense, reason, and intellect has intended us to forgo their use. --Galileo Galilei
When I reflect on so many profoundly marvelous things that persons have grasped, sought, and done, I recognize even more clearly that human intelligence is a work of God, and one of the most excellent. --Galileo Galilei
Our piety is deeper, the greater is our awareness of creation and its grandeur. --Johannes Kepler
We astronomers are priests of the highest God in regard to the book of nature. --Johannes Kepler
Thus I see plainly that the certainty and truth of all knowledge [scientiae] depends uniquely on my awareness of the true God, to such an extent that I was incapable of perfect knowledge [perfecte scire] about anything else until I became aware of him. -- Rene Decartes
There are two kinds of people one can call reasonable: those who serve God with all their heart because they know him, and those who seek him with all their heart because they do not know him. --Blaise Pascal
"The vastness, beauty, orderliness of heavenly bodies; the excellent structure of animals and plants; and other phenomena of nature justly induce an intelligent, unprejudiced observer to conclude a supreme, powerful, just, and good author." --Robert Boyle
Many if not all of these were Christians, so yes where this thought process originated was story-telling and narrative, but that doesn't mean that it leads one to think empirical study should not be used. As we can tell it lead to the opposite.
Do you pay attention to your emotions when you write? This is another mean-spirited thing to say. I understand you - I'm not an idiot. You don't need to call the other person stupid if it you - in fact, who is having the problem understanding the nature of the criticism I'm making.
Its not mean spirited to point out when you think someone isn't grasping a concept. You haven't made a criticism on the dilemma I've posed, everything I've responded to so far is off topic. Its all a red herring, but I felt it was interesting so I let us go down that rabbit hole.
Buddy - I've already answered this. When you scale back billions of years ago into the precambrian you have nothing but different versions of life. You are assuming that life only happened once. I am assuming that the life we see today is the life that survived.
Now, you seem to think that invertebrates HAD to be the ancestor for modern vertebrates. THAT IS NOT NECESSARY. You are completely overlooking how unnecessary that assumption is - but clearly this is where your focus lies. As I've already written - and to which you felt the need to ignore and then mock - invertebrates may be the evolutionary heir to a DIFFERENT EUKARYOTIC ANCESTOR. This is your issue - I've explained it, have told you that this is not that big a problem, but you apparently see it as the death of the evolutionary theory.
Okay and this is exactly what shows me you haven't completely grasped what the problem is. Let's say invertebrates did come from a different eukaryotic ancestor, then we have no evolutionary history for vertebrates in the fossil record. Are you saying we should just assume these vertebrates spontaneously arose from eukaryotic cells 500 million years ago with no evolutionary history to be found in the fossil record?!?? Where is the gradual evolution that takes a long time to occur? Where is the evidence of from this gradual process?? If we take your route we haven't solved the dilemma, the only other option is to say they came from invertebrates, but this puts us in a rock in a hard place as well due to the differences in mitochondria DNA. (To be continued next post)
Idiot, if everyone had the same sequence of nucleotides, everyone would look the same and be the same. The four base pairs make up the codons. And of course they are read differently because they code for different functional parts of an organism.
The alphabet is the database that's used to form words. In English it's "yes", Spanish "Si", French "Oui".
Get over it. Your sources are wrong. Not only are they wrong, but if they were right, the genetic code would be chaotic and there would be no genetic relationship among species on this planet. Common ancestry. It's so obvious that even one of your primate ancestors could figure it out.
No.. the truth is we observe gain in function in mutations leading to novel phenotype everywhere we look, from primates to plants. If you actually study this stuff you would know this.
originally posted by: ServantOfTheLamb
a reply to: flyingfish
No.. the truth is we observe gain in function in mutations leading to novel phenotype everywhere we look, from primates to plants. If you actually study this stuff you would know this.
Oh yea, lets ignore the work of people in the field because it doesn't fit my preconceived notions of how you think the world should work. I gave you the resources to show that everything you thought showed a gain in function mutation was not actually a gain in function mutation from the molecular perspective. If you wish to just assert I am ignorant an move on that is your right, but it isn't the intellectually honest route.
If you're not intentionally lying then you have some mental block preventing you from understanding basic biology. Why don't face the fact that you're no good at this. Novel phenotypes are gains in function.
originally posted by: ServantOfTheLamb
a reply to: flyingfish
If you're not intentionally lying then you have some mental block preventing you from understanding basic biology. Why don't face the fact that you're no good at this. Novel phenotypes are gains in function.
No they aren't. If you would cough of the ten bucks for the source I sent you, you would see that it addresses this very claim. All one has to do is read that source and they can tell that you are simply in denial.
Abstract
The central role of beneficial mutations for adaptive processes in natural populations is well established. Thus, there has been a long-standing interest to study the nature of beneficial mutations. Their low frequency, however, has made this class of mutations almost inaccessible for systematic studies. In the absence of experimental data, the distribution of the fitness effects of beneficial mutations was assumed to resemble that of deleterious mutations.
Abstract
Beneficial mutations are intuitively relevant to understanding adaptation 1, 2 and 3, yet not all beneficial mutations are of consequence to the long-term evolutionary outcome of adaptation. Many beneficial mutations—mostly those of small effect—are lost due either to (1) genetic drift 4 and 5 or to (2) competition among clones carrying different beneficial mutations, a phenomenon called the “Hill-Robertson effect” for sexual populations [6] and “clonal interference” for asexual populations [7]. Competition among clones becomes more prevalent with increasing genetic linkage and increasing population size, and it is thus generally characteristic of microbial populations 8 and 9. Together, these two phenomena suggest that only those beneficial mutations of large fitness effect should achieve fixation, despite the fact that most beneficial mutations produced are predicted to have very small fitness effects 10 and 11. Here, we confirm this prediction—both empirically and theoretically—by showing that fitness effects of fixed beneficial mutations follow a distribution whose mode is positive.
These results suggest that the initial step in adaptive evolution—the production of novel beneficial mutants from which selection sorts—is very general, being characterized by an approximately exponential distribution with many mutations of small effect and few of large effect. We also document substantial variation in the pleiotropic costs of antibiotic resistance, a result that may have implications for strategies aimed at eliminating resistant pathogens in animal and human populations.
Sequence analysis showed that the Dominant white allele was exclusively associated with a 9-bp insertion in exon 10, leading to an insertion of three amino acids in the PMEL17 transmembrane region. Similarly, a deletion of five amino acids in the transmembrane region occurs in the protein encoded by Dun. The Smoky allele shared the 9-bp insertion in exon 10 with Dominant white, as expected from its origin, but also had a deletion of 12 nucleotides in exon 6, eliminating four amino acids from the mature protein. These mutations are, together with the recessive silver mutation in the mouse, the only PMEL17 mutations with phenotypic effects that have been described so far in any species.
Abstract Lipoprotein lipase (LPL) hydrolyzes triglycerides in the circulation and promotes the hepatic uptake of remnant lipoproteins. Since the gene was cloned in 1989, more than 100 LPL gene mutations have been identified, the majority of which cause loss of enzymatic function. In contrast to this, the naturally occurring LPLS447X variant is associated with increased lipolytic function and an anti-atherogenic lipid profile and can therefore be regarded as a gain-of-function mutation.
Abstract Hereditary persistence of fetal hemoglobin (HPFH) is a benign condition in which the normal shutoff of fetal hemoglobin (Hb F) production fails to occur. In the G gamma beta+ type of HPFH, erythrocytes of adult heterozygotes contain approximately equal to 20% Hb F, which is almost exclusively of the G gamma-globin variety, without increased levels of gamma-globin chains from the nearby A gamma-globin gene. Unlike some forms of HPFH, no major deletions in the globin gene cluster have been found by genomic blotting in the G gamma beta+ variety. We report here a family with this condition, from which cosmid clones of the beta-globin gene cluster from the G gamma beta+ HPFH allele have been obtained. Sequencing around the fetal genes has identified a point mutation 202 base pairs 5' to the G gamma-globin gene that is present in genomic DNA of 3/3 unrelated individuals with G gamma beta+ HPFH but in none of more than 100 non-HPFH individuals.
This is the second time you have tried to make it appear as I said everything needs to have the same sequence of nucleotides, when I have never said or implied anything of the sort. You are being dishonest. I don't think you understand that we are comparing the interpretation of the same codon in two different organisms. Many organisms use the Standard Code which is why for a long time we thought there was a tree of life. Now we know that is wrong. Organisms that don't interpret the same codon in the same way cannot be related.
The origin of eukaryotes was one of life’s major evolutionary transitions (1, 2). Despite much progress in recent years, the issue is far from being resolved to everyone’s satisfaction. There is broad agreement that the last eukaryotic common ancestor (LECA) possessed numerous features that are lacking in prokaryotes, including a mitochondrion, a nucleus, an extensive endomembrane traffic system, meiosis, sex, spliceosomal introns, a eukaryotic flagellum, a cytoskeleton, and the like (2, 3).
The order of events that gave rise to those attributes is still debated (3–5), as are issues concerning (i) the number and nature of prokaryotic partners that were involved in eukaryotic symbioses, (ii) the role of gene transfers from the ancestral mitochondrion, and (iii) the possible role of lateral gene transfer (LGT) from donors that were distinct from the mitochondrial (or plastid) endosymbiont, or its host. Three recent developments have shed new light on the problem of eukaryote origins.
The first is the insight that the host for the origin of eukaryotes is now best understood as a gardenvariety archaeon, one that branches within the diversity of known archaeal lineages (4, 6–9). An origin of the host from within the TACK superphylum (4, 7, 9) is the position most widely discussed at present, but the TACK superphylum was itself only recently recognized through the discovery of new archaeal lineages (7). It is possible that, as new archaeal lineages become discovered, the phylogenetic arrangement of eukaryotes and archaea might undergo further adjustments still (10).
A second development is the recognition that the origin of the roughly 2,000 gene families that underpinned the origin of eukaryotic-specific traits in the eukaryote ancestor required the biochemical power of internalized bioenergetic membranes that mitochondria provided (3). Mitochondria, not oxygen, made the energetic difference that separates eukaryotes from prokaryotes. That is because anaerobic mitochondria generate about five ATP per glucose and fermentations in eukaryotes generate two to four ATP per glucose (11), such that the meager 5- to 10-fold increase in ATP yield per glucose conferred by oxygen respiration is dwarfed by the 104 to 105 increase in ATP yield per gene manifest in cells with mitochondria (3). The key to the orders of magnitude increase in energy available for evolutionary invention that mitochondria conferred is the eukaryotic configuration of internal, compartmentalized bioenergetic membranes relative to genes (3, 5). After all, had oxygen been the key to eukaryote complexity, Escherichia coli would have become eukaryotic for the same reason. Furthermore, eukaryotic aerobes and anaerobes interleave across eukaryote phylogeny (11), and bioenergetics point to a mitochondrion ancestor with a facultatively anaerobic lifestyle (12). Only those cells became complex that experienced the increased energy per gene afforded by mitochondria, and the long puzzling lack of true intermediates in the prokaryote– eukaryote transition has a bioenergetic cause (3).
A third, and more involved, development is the recognition of genomic chimerism in eukaryotes (13), an issue that has been brewing for some time (13–22). Genome analyses showed that genes of bacterial origin outnumber genes of archaeal origin in yeast (21) and other eukaryotic genomes (23, 24) by a factor of about 3:1 and that roughly 15–20% of the nuclear genes in photosynthetic eukaryotes are acquisitions attributable to the endosymbiotic origin of plastids from cyanobacteria (25–27). However, many of the gene acquisitions in photosynthetic eukaryotes do not trace, in gene trees, directly to a cyanobacterial, and thus obviously plastid, origin.
Conclusion
Inherited chimerism is an alternative to the problematic practice of conjuring up additional, gene-donating symbionts at organelle origins to explain gene trees. It merely requires a selective force to associate the symbiont (either plastid or mitochondrion) to its host so that the endosymbiosis (one cell living within another) can be established and gene transfer from the symbiont can commence. It places no constraints on the collections of genes that the plastid and the mitochondrial symbionts possessed, other than that it needs to be a genome-sized collection, not tens of thousands of genes, and it allows freely for LGT among prokaryotes before the endosymbionts become organelles and afterward. LGT among prokaryotes has received much attention in the past decades. Inherited chimerism incorporates LGT among prokaryotes into endosymbiotic theory
Oh yea my peer reviewed sources are wrong because some guy on a blog says so....I'll stick with my sources over you anyday...