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Icons of Evolution

Buzzard3

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Evolutionary theory is used for tracking changes it's also function as a guide for examining animals. Genetics is one pathway and inherited traits are understood via the demonstrated mechanisms of evolution.
... none of which depends on the theory of common descent (ie, all life on earth descended from a common ancestor).
 
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Warden_of_the_Storm

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... none of which depends on the theory of common descent.

Knowing how inherited traits work doesn't depend on the theory of common descent...
 
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Buzzard3

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Knowing how inherited traits work doesn't depend on the theory of common descent...
Exactly. The theory of common descent is irrelevant and useless to medical research and every other form of applied science.
 
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Warden_of_the_Storm

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Exactly. The theory of common descent is irrelevant and useless to medical research and every other form of applied science.

No, my comment was made in disbelief that you could say that in all seriousness when it's a contradictory statement.

Though saying that, maybe you can actually explain HOW and WHY the theory of common descent is irrelevant and useless to medical research and every other form of applied science. Saying it is and showing why it is are two very different things after all.
 
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Buzzard3

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Privately???
What I should have said is, all atheist scientists privately believe that the theory of evolution is the truth, but publicly they say they accept ToE as the best available scientific explanation.
 
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Buzzard3

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View attachment 367173
"According to a 1998 survey of members of the National Academy of Sciences (NAS), nearly 95% of NAS biologists identify themselves as either atheists or agnostics, a percentage of unbelief far higher than in any other scientific discipline ...

Similarly, according to a 2003 Cornell survey of leading scientists in the field of evolution, 87% deny existence of God, 88% disbelieve in life after death, and 90% reject idea that evolution directed toward “ultimate purpose.”"


"In “Evolution, Religion and Free Will� (American Scientist, Volume 95, 294ff), Gregory W. Graffin and William B. Provine found that, of 149 eminent evolutionists polled, 78% were pure naturalists (no God) and only two were clearly theists (traditional idea of God) ...

They note that the evolutionary biologists scored the lowest so far in any such poll. They described the vast majority of their respondents as “metaphysical naturalists�, “materialists�, and “monists�. In other words, these are people who are serious about their materialism and atheism."

 
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Buzzard3

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No, my comment was made in disbelief that you could say that in all seriousness when it's a contradictory statement.

Though saying that, maybe you can actually explain HOW and WHY the theory of common descent is irrelevant and useless to medical research and every other form of applied science. Saying it is and showing why it is are two very different things after all.
Please provide an example of how the theory that all life on earth descended from a common ancestor has proven useful in medical science.
 
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Buzzard3

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The development of new antibiotics to combat the evolution of resistant strains of bacteria provides an excellent example of the application of the theory of evolution.

AspectEvolutionary PrincipleHow Pathogens Use It to Evolve ResistanceSpecific Ancestor ExampleHow Medicine Uses Evolution to Counter Resistance
MutationRandom genetic change introduces variationSpontaneous mutations in bacterial genes confer resistance (e.g., rpsL)Mycobacterium tuberculosis H37Rv (pre-streptomycin)Screen for naturally occurring bacterial compounds (e.g., streptomycin); use mutagenesis to find weak spots in bacteria
Natural SelectionFitter variants survive and reproduceDrug-resistant strains survive treatment and dominateStaphylococcus aureus 8325-4 (pre-penicillin resistance)Use high-throughput evolution models to simulate resistance and pre-select drugs less likely to fail
Variation within PopulationsGenetic diversity affects survival outcomesResistant subpopulations survive while others dieMycobacterium tuberculosis wild strains (mixed katG variants)Tailor combination therapy (e.g., rifampin + isoniazid) to minimize survival of diverse resistant clones
AdaptationPopulations evolve to changing environmentsEnterococcus faecium evolves vancomycin resistance via vanA genesE. faecium DO (vancomycin-sensitive)Develop next-generation antibiotics targeting new pathways (e.g., linezolid targeting protein synthesis)
Survival of the FittestMost fit reproduce in the new environmentMDR strains outcompete sensitive ones in drug-rich environmentsKlebsiella pneumoniae ATCC 13883Rotate or cycle antibiotics in hospitals to reduce selective pressure on any one resistance trait
Selective PressureEnvironmental conditions shape evolutionAntibiotic overuse selects resistant bacteriaE. coli K-12 (pre-fluoroquinolone resistance)Use antimicrobial stewardship to reduce unnecessary pressure; limit broad-spectrum drug use
Co-evolutionInteracting species evolve in responseBacteria develop β-lactamases, we develop β-lactamase inhibitorsH. influenzae Rd KW20 (non–β-lactamase producer)Design inhibitors (e.g., clavulanic acid) based on enzyme evolution structure modeling
Evolutionary Arms RaceOngoing adaptations between rivalsPathogens modify surface proteins to evade immunityBordetella pertussis Tohama IContinuously update vaccine components (e.g., DTaP formulation changes) to match new variants
Genetic Drift / Gene FlowRandom changes & horizontal gene transferResistance genes spread across species (e.g., CTX-M plasmids)E. coli K-12 & Klebsiella MGH 78578 (pre-ESBL)Use genomic surveillance to monitor plasmid transmission and inform targeted antibiotic policies
Predictive Power of EvolutionEvolutionary models can forecast changeStreptococcus pneumoniae shifts to non-vaccine serotypesS. pneumoniae D39 (serotype 2)Predict future mutations and preemptively design mRNA or conjugate vaccines (e.g., PCV13, mRNA COVID-19 updates)
... none of which depend on the theory that all life on earth evolved from a common ancestor.
 
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Fervent

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"According to a 1998 survey of members of the National Academy of Sciences (NAS), nearly 95% of NAS biologists identify themselves as either atheists or agnostics, a percentage of unbelief far higher than in any other scientific discipline ...

Similarly, according to a 2003 Cornell survey of leading scientists in the field of evolution, 87% deny existence of God, 88% disbelieve in life after death, and 90% reject idea that evolution directed toward “ultimate purpose.”"


"In “Evolution, Religion and Free Will� (American Scientist, Volume 95, 294ff), Gregory W. Graffin and William B. Provine found that, of 149 eminent evolutionists polled, 78% were pure naturalists (no God) and only two were clearly theists (traditional idea of God) ...

They note that the evolutionary biologists scored the lowest so far in any such poll. They described the vast majority of their respondents as “metaphysical naturalists�, “materialists�, and “monists�. In other words, these are people who are serious about their materialism and atheism."

This reminds me of the old adage about lies, [big] lies, and statistics. There's clear monkeying with the numbers to drive a narrative. But let's get out the pitchforks.
 
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sjastro

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... none of which depend on the theory that all life on earth evolved from a common ancestor.
Regretfully you can't stick to the same story as I was responding to this.
Buzzard3:
A theory that attempts to describe the process that produced the history of life isn't "exceedingly useful" in producing medications ... it's exceedingly useless.
Here is the table again for reference.
AspectEvolutionary PrincipleHow Pathogens Use It to Evolve ResistanceSpecific Ancestor ExampleHow Medicine Uses Evolution to Counter Resistance
MutationRandom genetic change introduces variationSpontaneous mutations in bacterial genes confer resistance (e.g., rpsL)Mycobacterium tuberculosis H37Rv (pre-streptomycin)Screen for naturally occurring bacterial compounds (e.g., streptomycin); use mutagenesis to find weak spots in bacteria
Natural SelectionFitter variants survive and reproduceDrug-resistant strains survive treatment and dominateStaphylococcus aureus 8325-4 (pre-penicillin resistance)Use high-throughput evolution models to simulate resistance and pre-select drugs less likely to fail
Variation within PopulationsGenetic diversity affects survival outcomesResistant subpopulations survive while others dieMycobacterium tuberculosis wild strains (mixed katG variants)Tailor combination therapy (e.g., rifampin + isoniazid) to minimize survival of diverse resistant clones
AdaptationPopulations evolve to changing environmentsEnterococcus faecium evolves vancomycin resistance via vanA genesE. faecium DO (vancomycin-sensitive)Develop next-generation antibiotics targeting new pathways (e.g., linezolid targeting protein synthesis)
Survival of the FittestMost fit reproduce in the new environmentMDR strains outcompete sensitive ones in drug-rich environmentsKlebsiella pneumoniae ATCC 13883Rotate or cycle antibiotics in hospitals to reduce selective pressure on any one resistance trait
Selective PressureEnvironmental conditions shape evolutionAntibiotic overuse selects resistant bacteriaE. coli K-12 (pre-fluoroquinolone resistance)Use antimicrobial stewardship to reduce unnecessary pressure; limit broad-spectrum drug use
Co-evolutionInteracting species evolve in responseBacteria develop β-lactamases, we develop β-lactamase inhibitorsH. influenzae Rd KW20 (non–β-lactamase producer)Design inhibitors (e.g., clavulanic acid) based on enzyme evolution structure modeling
Evolutionary Arms RaceOngoing adaptations between rivalsPathogens modify surface proteins to evade immunityBordetella pertussis Tohama IContinuously update vaccine components (e.g., DTaP formulation changes) to match new variants
Genetic Drift / Gene FlowRandom changes & horizontal gene transferResistance genes spread across species (e.g., CTX-M plasmids)E. coli K-12 & Klebsiella MGH 78578 (pre-ESBL)Use genomic surveillance to monitor plasmid transmission and inform targeted antibiotic policies
Predictive Power of EvolutionEvolutionary models can forecast changeStreptococcus pneumoniae shifts to non-vaccine serotypesS. pneumoniae D39 (serotype 2)Predict future mutations and preemptively design mRNA or conjugate vaccines (e.g., PCV13, mRNA COVID-19 updates)

Explain how the theory of evolution is useless in the development of medicines.
 
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Warden_of_the_Storm

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Please provide an example of how the theory that all life on earth descended from a common ancestor has proven useful in medical science.

Not playing this game. You said "The theory of common descent is irrelevant and useless to medical research and every other form of applied science."

You've not said how or why. Answer that question.
 
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Fervent

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Please provide an example of how the theory that all life on earth descended from a common ancestor has proven useful in medical science.
Please provide an example of someone who has argued that.

May as well ask how the theory of stellar evolution has proven useful in medical science. No one has made the claim, so all you are doing is presenting a straw objection.
 
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Hans Blaster

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May as well ask how the theory of stellar evolution has proven useful in medical science. No one has made the claim, so all you are doing is presenting a straw objection.
Well...

If you want to turn inorganic matter into living organic matter (as was briefly mentioned over the weekend on one of these threads) you will definitely need stellar evolution to cook up some carbon. :)
 
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Fervent

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Well...

If you want to turn inorganic matter into living organic matter (as was briefly mentioned over the weekend on one of these threads) you will definitely need stellar evolution to cook up some carbon. :)
Playing the long game, I see
 
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Buzzard3

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Regretfully you can't stick to the same story as I was responding to this.

Here is the table again for reference.
AspectEvolutionary PrincipleHow Pathogens Use It to Evolve ResistanceSpecific Ancestor ExampleHow Medicine Uses Evolution to Counter Resistance
MutationRandom genetic change introduces variationSpontaneous mutations in bacterial genes confer resistance (e.g., rpsL)Mycobacterium tuberculosis H37Rv (pre-streptomycin)Screen for naturally occurring bacterial compounds (e.g., streptomycin); use mutagenesis to find weak spots in bacteria
Natural SelectionFitter variants survive and reproduceDrug-resistant strains survive treatment and dominateStaphylococcus aureus 8325-4 (pre-penicillin resistance)Use high-throughput evolution models to simulate resistance and pre-select drugs less likely to fail
Variation within PopulationsGenetic diversity affects survival outcomesResistant subpopulations survive while others dieMycobacterium tuberculosis wild strains (mixed katG variants)Tailor combination therapy (e.g., rifampin + isoniazid) to minimize survival of diverse resistant clones
AdaptationPopulations evolve to changing environmentsEnterococcus faecium evolves vancomycin resistance via vanA genesE. faecium DO (vancomycin-sensitive)Develop next-generation antibiotics targeting new pathways (e.g., linezolid targeting protein synthesis)
Survival of the FittestMost fit reproduce in the new environmentMDR strains outcompete sensitive ones in drug-rich environmentsKlebsiella pneumoniae ATCC 13883Rotate or cycle antibiotics in hospitals to reduce selective pressure on any one resistance trait
Selective PressureEnvironmental conditions shape evolutionAntibiotic overuse selects resistant bacteriaE. coli K-12 (pre-fluoroquinolone resistance)Use antimicrobial stewardship to reduce unnecessary pressure; limit broad-spectrum drug use
Co-evolutionInteracting species evolve in responseBacteria develop β-lactamases, we develop β-lactamase inhibitorsH. influenzae Rd KW20 (non–β-lactamase producer)Design inhibitors (e.g., clavulanic acid) based on enzyme evolution structure modeling
Evolutionary Arms RaceOngoing adaptations between rivalsPathogens modify surface proteins to evade immunityBordetella pertussis Tohama IContinuously update vaccine components (e.g., DTaP formulation changes) to match new variants
Genetic Drift / Gene FlowRandom changes & horizontal gene transferResistance genes spread across species (e.g., CTX-M plasmids)E. coli K-12 & Klebsiella MGH 78578 (pre-ESBL)Use genomic surveillance to monitor plasmid transmission and inform targeted antibiotic policies
Predictive Power of EvolutionEvolutionary models can forecast changeStreptococcus pneumoniae shifts to non-vaccine serotypesS. pneumoniae D39 (serotype 2)Predict future mutations and preemptively design mRNA or conjugate vaccines (e.g., PCV13, mRNA COVID-19 updates)

Explain how the theory of evolution is useless in the development of medicines.
That depends on what you mean by "the theory of evolution", for there are different interpretations of that term.
If by "the theory of evolution" you mean the mechanisms of evolution (as your posts suggest), please be advised that I never claimed that the mechanisms of evolution (as listed in your posts) are "useless in the development of medicines".

My argument is that the theory of common descent (that all life on earth descended from a common ancestor - often referred to as the theory of evolution) is useless in the field of medical science.
 
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Buzzard3

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No, my comment was made in disbelief that you could say that in all seriousness when it's a contradictory statement.
Please explain why it's a "contradictory statement".
 
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Buzzard3

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Not playing this game. You said "The theory of common descent is irrelevant and useless to medical research and every other form of applied science."

You've not said how or why. Answer that question.
If no one is aware of any use for the theory of common descent in medical or biological research, it's a fair guess that none exist.
 
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Buzzard3

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Please provide an example of someone who has argued that.

May as well ask how the theory of stellar evolution has proven useful in medical science. No one has made the claim, so all you are doing is presenting a straw objection.
Stephen W. Schaeffer (Professor Emeritus of Biology) claims that the theory of common descent has proven useful in identifying so-called conserved sequences in human DNA (if "conserved", such sequences are understood to serve a functional purpose ... as opposed to so-called junk DNA, which is generally understood to serve no functional purpose).

My understanding is that process involves comparing human and chimps DNA, then finding similar DNA sequences, which are alleged (according to the theory of common descent) to have been "conserved" by natural selection from a common ancestor.

But it seems debatable to me if identifying conserved sequences has actually proven fruitful in curing or improving the treatment of any disease.
 
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sjastro

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That depends on what you mean by "the theory of evolution", for there are different interpretations of that term.
If by "the theory of evolution" you mean the mechanisms of evolution (as your posts suggest), please be advised that I never claimed that the mechanisms of evolution (as listed in your posts) are "useless in the development of medicines".

My argument is that the theory of common descent (that all life on earth descended from a common ancestor - often referred to as the theory of evolution) is useless in the field of medical science.
A common mistake made by individuals who are unfamiliar with science is to confuse theory with interpretation. There is only one theory of evolution defined by the drivers of evolution in the Aspect column of the table. (The exception is the last entry since predictive power is not a driver but a strength of the theory).
Interpretation is more nuanced where a particular aspect of the theory such as whether the dominant spread of genetic change is due to natural selection or genetic drift which does not alter the theory itself.

Then there is the application of the theory such as the development of strain resistant antibiotics as defined in the table where the same evolutionary drivers are used which also explains a common ancestor to all life forms. You cannot divorce the two.
 
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