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originally posted by: Krazysh0t
originally posted by: WarminIndy
See the circular reasoning?
Darwinism is not true -> we have discovered more since Darwinism -> evolution is true because Darwin told us about it -> Darwinism is not true
If the whole premise of Darwinism was faulty, then anything built on it is faulty, yet somehow Darwinism is defended. Circular reasoning.
How many times does it have to be explained to you that modern evolutionary theory is built on Darwinian evolution? Darwinian evolution isn't 100% wrong, Darwin got the basic gist of how it works, he just didn't have all the available evidence that we do today and detailed an incomplete picture. The reason Darwinian evolution doesn't enter into modern evolutionary debates is because of this reason. That is like trying to say that because a Model T car cannot reach the speed of 120 miles per hour, a modern day race car is unable to do it. It is absurd and a VERY poor example of a circular reasoning. You want a GOOD example of circular reasoning?
How do we know the bible is true? It is the divine inspired word of god
How do we know that the bible is the divine inspired word of god? The bible says so.
As for the rest of your fallacies. Who cares? They don't pertain to evolution being true or not. I mean they are certainly valid fallacies, but they are irrelevant to the discussion because they neither prove nor disprove evolution. Though going by your tendency to embellish or conflate details, as can be seen from your example about peter vlar's work, I'd wager that these fallacies didn't work out the way you are describing them in this thread.
originally posted by: WarminIndy
originally posted by: Krazysh0t
originally posted by: WarminIndy
See the circular reasoning?
Darwinism is not true -> we have discovered more since Darwinism -> evolution is true because Darwin told us about it -> Darwinism is not true
If the whole premise of Darwinism was faulty, then anything built on it is faulty, yet somehow Darwinism is defended. Circular reasoning.
How many times does it have to be explained to you that modern evolutionary theory is built on Darwinian evolution? Darwinian evolution isn't 100% wrong, Darwin got the basic gist of how it works, he just didn't have all the available evidence that we do today and detailed an incomplete picture. The reason Darwinian evolution doesn't enter into modern evolutionary debates is because of this reason. That is like trying to say that because a Model T car cannot reach the speed of 120 miles per hour, a modern day race car is unable to do it. It is absurd and a VERY poor example of a circular reasoning. You want a GOOD example of circular reasoning?
How do we know the bible is true? It is the divine inspired word of god
How do we know that the bible is the divine inspired word of god? The bible says so.
As for the rest of your fallacies. Who cares? They don't pertain to evolution being true or not. I mean they are certainly valid fallacies, but they are irrelevant to the discussion because they neither prove nor disprove evolution. Though going by your tendency to embellish or conflate details, as can be seen from your example about peter vlar's work, I'd wager that these fallacies didn't work out the way you are describing them in this thread.
So now what? Do you continue in the fallacies during arguments?
That's the point of the whole discussion, because the fallacies are now pop culture, so how will you convince pop culture that the next scientific theory is valid if they hold on to the last one?
You still assume this is against scientific methods. No, this is about how the interpretations are forced into pop culture.
originally posted by: WarminIndy
Premises - it is assumed that all Christians are against science.
Faulty premise because there are scientists who are Christians.
Inference - it is inferred that Christians are not educated, therefore stupid.
Faulty inference - many Christians are highly intellectual and educated.
faulty argumentum - The premise for Christianity is that God does exist. Which takes us back to the original logical fallacy. What makes this faulty is that not every Christian doctrine is understood. Christians also teach Christian charity because the founder of the religion who was historical made historical claims to be nice to your neighbors and yet all religions teach a Golden Rule. Even non-religious people accept the Golden Rule. So the ad ignoratum is that all Christians must be wrong about all of premise, even though part of the premise is shared among all people groups.
Argumentum ad misericordiam - fallacy here because I don't think this one has been presented by either side.
Argumentum ad populum - this logical fallacy is that on this thread the claims have been made that religion is detrimental
Faulty ad populum - Religions have offered good things to society.
See, we could go on. If there is to be true debate, then the faulty logic must be removed in order to discuss anything. I never said religious people were against science, that was a charge made against religious people.
Darwinism is not true -> we have discovered more since Darwinism -> evolution is true because Darwin told us about it -> Darwinism is not true
If the whole premise of Darwinism was faulty, then anything built on it is faulty, yet somehow Darwinism is defended. Circular reasoning.
originally posted by: WarminIndy
What I am objecting to is this...people don't allow the scientists who do use science and employ the scientific methods to even be heard in the first place. All of this jumping the gun isn't helpful.
What I DID say is that I believe in the possibility of an Intelligence that designed the natural world, including the process of evolution.
I DID question the theories of speciation. I asked that if an individual in a population does not mutate at the same rate, is that individual no longer a member of the species.
But I was told that speciation and evolution is observed in evolution for a population. I was wondering then how that is, considering that populations are made of individuals. If evolution occurs at the population level, then what processes are occurring that some individuals evolve further than others, within the same population group.
Either the whole population of individuals evolve at the same rate, hence speciation, or there are differences in mutations occurring that make the individuals not as evolved.
So what process is occurring for the entire population? When experiments have been done, they have stated that it shows that not all evolve in the same way, and not all evolve to the same degree.
But you, are you an evolved member of the species group, or are you a highly adapted individual in the highly adapted species group?
Is the whole species group highly adapted? I am sure that not every individual in the Homo Sapien group is as adapted in the same respect.
natural selection certainly then favors certain individuals, and then that's why certain traits are passed on. But what makes an individual favored to carry these traits?
But does the recombination lead to a more highly adaptable individual? This is the question that Darwin was proposing when he said "Favored Races".
where is the evidence of any eukaryote from the eukaryotic population?
It then doesn't seem to me that mutations are just random or that natural selection is what guides, because of the vastly different genetic populations and yet your chromosomes can only hold so much information from your ancestors. If mutations are random, then it would be a totally random thing to have individuals in the same population group to be completely different than others in the same group.
But this is speciation, which is populations that share similarity. It doesn't seem to work that way when certain population groups have unique markers. Are they evolved or are they adapated? And if they are adapted, then to what purpose?
pop·u·la·tion
ˌpäpyəˈlāSHən/Submit
noun
all the inhabitants of a particular town, area, or country.
"the island has a population of about 78,000"
synonyms: inhabitants, residents, people, citizens, citizenry, public, community, populace, society, body politic, natives, occupants; formaldenizens
"a new social agenda for the population of these emerging nations"
a particular section, group, or type of people or animals living in an area or country.
"the country's immigrant population"
the specified extent or degree to which an area is or has been populated.
"areas of sparse population"
In biology, populations are groups of individuals belonging to the same species that live in the same region at the same time. Population density is a measure of the number of organisms that make up a population in a defined area.
Nature has selected for people with darker skin in tropical latitudes, especially in nonforested regions, where ultraviolet radiation from the sun is usually the most intense.
By doing this, it helps to prevent sunburn damage that could result in DNA changes and, subsequently, several kinds of malignant skin cancers.
e. Since the Sun radiance varies to some extent over short and long periods (Fröhlich 1991), the solar constant does not remain steady over time. There is a variation of about ± 1 Wm-2 around the mean solar constant during a typical Sun cycle of 11 years (Gueymard and Myers 2008)
Terrestrial Spectra
The spectrum of the solar radiation at the earth's surface has several components (see Fig. 2). Direct radiation comes straight from the sun, diffuse radiation is scattered from the sky and from the surroundings. Additional radiation reflected from the surroundings (ground or sea) depends on the local "albedo." The total ground radiation is called the global radiation. The direction of the target surface must be defined for global irradiance. For direct radiation the target surface faces the incoming beam.
The Changing Terrestrial Solar Spectrum
Absorption and scattering levels change as the constituents of the atmosphere change. Clouds are the most familiar example of change; clouds can block most of the direct radiation. Seasonal variations and trends in ozone layer thickness have an important effect on terrestrial ultraviolet level.
Standard Spectra
Solar radiation reaching the earth's surface varies significantly with location, atmospheric conditions including cloud cover, aerosol content, and ozone layer condition, and time of day, earth/sun distance, solar rotation and activity. Since the solar spectra depend on so many variables, standard spectra have been developed to provide a basis for theoretical evaluation of the effects of solar radiation and as a basis for simulator design. These standard spectra start from a simplified (i.e. lower resolution) version of the measured extraterrestrial spectra, and use sophisticated models for the effects of the atmosphere to calculate terrestrial spectra.
originally posted by: WarminIndy
Lions live in Africa, kangaroos live in Australia, except for zoos in Stockholm or Berlin. But naturally, those animals typically remain in their own geographic regions. Therefore, they are adapted to live in their environments, yes?
But humans can live anywhere, reasonably, except for in water. They can live in Arctic or Antarctic regions only with the ability themselves to adapt, but never naturally.
And that's what I am trying to say, if a human population can live naturally anywhere, except those places, then why have humans not reverted to being able to live in the water? We don't see Polynesians that have devolved or reverted to being able to live in water.
So my point was, given that species are considered populations, and species are subject to evolution, then it can only occur at the individual level, even though evolution is counted at the population level. So if a group of people are naturally adapted through random means, then human population groups must have been adapted for specific geographic regions, individually.
And yet human population groups are capable of living in Tropical zones and still remain a particular skin color. Hence, Richard Dawkins is a white European that grew up in Africa. So who in his family was adapted for him to remain with very little change that Richard Dawkins remains as Caucasian, living in the very zone that nature selects for people to have dark skin tones?
So did the evolution of certain groups occur in one particular locations or did it occur after certain individuals went to another location?
originally posted by: peter vlar
originally posted by: WarminIndy
Lions live in Africa, kangaroos live in Australia, except for zoos in Stockholm or Berlin. But naturally, those animals typically remain in their own geographic regions. Therefore, they are adapted to live in their environments, yes?
But humans can live anywhere, reasonably, except for in water. They can live in Arctic or Antarctic regions only with the ability themselves to adapt, but never naturally.
And that's what I am trying to say, if a human population can live naturally anywhere, except those places, then why have humans not reverted to being able to live in the water? We don't see Polynesians that have devolved or reverted to being able to live in water.
theres no such thing as Devolving. Evolution is the sum of genetic changes over time, that all. There is no forward or backwards or most evolved or less evolved.
So my point was, given that species are considered populations, and species are subject to evolution, then it can only occur at the individual level, even though evolution is counted at the population level. So if a group of people are naturally adapted through random means, then human population groups must have been adapted for specific geographic regions, individually.
that still doesn't put it at an individual level. You're over thinking it and trying to make it more complicated than it is.
And yet human population groups are capable of living in Tropical zones and still remain a particular skin color. Hence, Richard Dawkins is a white European that grew up in Africa. So who in his family was adapted for him to remain with very little change that Richard Dawkins remains as Caucasian, living in the very zone that nature selects for people to have dark skin tones?
I'm sorry but that's so far outside the bounds of any biological or anthropological theory or hypothesis that it's almost insane. Just because he can survive in that environment with modern technology doesn't mean he would have thrived in it let alone been able to pass on his genes if he were to have spent the rest of his days their. This is some serious mental gymnastics to get this to appear logical, I'm sorry.
So did the evolution of certain groups occur in one particular locations or did it occur after certain individuals went to another location?
Both. Anatomically modern humans evolved in East Africa, the oldest confirmed remains are from Ethiopia and are over 160,000 years old. The initial adaptation is for that climate. As humans moved out of Africa and into other ecological niches, they slowly adapted to those as well.
originally posted by: Tangerine
originally posted by: peter vlar
originally posted by: WarminIndy
This is a game she plays. My suggestion is to not feed into it.
Mitochondrial DNA (mtDNA) has been a marker of choice for reconstructing historical patterns of population demography, admixture, biogeography and speciation. However, it has recently been suggested that the pervasive nature of direct and indirect selection on this molecule renders any conclusion derived from it ambiguous
The study of evolution frequently requires understanding the history of the population, species or clade under study. In population genetics, a recent history of population bottlenecks may restrict genetic variation and thus constrain the speed of adaptation. In examining diversification over space, we need to have detailed knowledge of the different populations' histories of colonization and the gene flow between them
Thirdly, as an area of at least low recombination, the whole molecule can be assumed to have the same genealogical history.
This analysis shows that the putative secondary/intermediate LHON mutations 4216, 4917, 13708, 15257, and 15812 are ancient polymorphisms, are associated in specific combinations, and define two common Caucasoid-specific haplotype groupings (haplogroups J and T). On the contrary, the same analysis shows that the primary mutations 11778, 3460, and 14484 are recent and are due to multiple mutational events. However, phylogenetic analysis also reveals a different evolutionary pattern for the three primary mutations. The 3460 mutations are distributed randomly along the phylogenetic trees, without any preferential association with the nine haplogroups (H, I, J, K, T, U, V, W, and X) that characterize European populations, whereas the 11778 and 14484 mutations show a strong preferential association with haplogroup J. This finding suggests that one ancient combination of haplogroup J-specific mutations increases both the penetrance of the two primary mutations 11778 and 14484 and the risk of disease expression.
The JT tree (outlined in Figure 1; see Figures S1 and S2 for details) confirms the presence of two main phylogenetic clusters, J and T, with no intermediates. The ML age estimates suggest that JT arose ∼58 ka ago, probably before the settlement of the Fertile Crescent according to current evidence, and that J and T diverged within the timeframe of settlement in the Fertile Crescent, ∼40 ka (with ML; ∼35 ka with ρ) and ∼30 ka ago, respectively (Table 1). Fragments of both J and T now extend well beyond their core Near Eastern and European range into North Africa, the Indian subcontinent, and central Asia
Like haplogroup J, haplogroup T falls into two distinct subclades, T1 and T2. However, the structure of these subclades is more complex than that of the five nested subclades found in J. Both T1 and T2 include several paraphyletic lineages, and whereas T1 falls into just two nested subclades, T2 displays at least nine, although a single one, T2b, encompasses about half of T2 among Europeans.
The early presence of T2 in Europe (even with the assumption that it arose in the Near East) suggests that ancestors of T2b might have been present in Europe well before the age of T2b itself, at any time back to the LGM, although T2b seems to have been dispersed within Europe during the early Neolithic period.
Several minor T2 subclades, such as T2g, T2h, and T2i, are found in both Europe and the Near East and remain enigmatic. Additional subclades, represented by only two complete mtDNAs each, along with many more paraphyletic members of T2, have so far been seen almost exclusively in Europe and date collectively (as a paragroup) to the Late Glacial period.
Our analysis confirms that haplogroups J and T and their major subclades (J1 and J2, T1 and T2) most likely arose in the Near East between the time of first settlement by modern humans and the LGM
It seems plausible to regard JT and U as belonging to members of the same early human group, ancestral to both Near Easterners and Europeans.
Indeed, the major T2 lineage, T2b, although displaying a star-like pattern dating to ∼10 ka ago, suggesting an expansion across Europe at the time of the early Neolithic period, may well have arisen indigenously within Europe from a T2 ancestor.
It was recognized at the outset that mtDNA was strictly a marker for historical processes in females; should male and female history differ in a species, then this marker would not reflect the history of the species as a whole but that of the female portion.
I don't think anybody has claimed that in this thread. Folks are talking about biblical literalists aka Christian fundamentalists. Nobody said all Christians are against science.
originally posted by: WarminIndy
a reply to: peter vlar
Thank you for the science discussion. I recognize that this is your field, but as a layperson, I still have the right to ask questions.
Now, about mtDNA haplotypes, mine is T2b, so that's where I focus most of my energy at, understanding the T clade and my subclade T2b.
I mentioned bottlenecked populations.
OK for understanding T2b, we have to know the history of the population in question, so I will focus on T2b, if that is ok.
So if there is a decreased speed of adaptation, then my statement that certain populations do not adapt as the same rate still holds.
I asked in the context of recombination and here is the what the author says
Thirdly, as an area of at least low recombination, the whole molecule can be assumed to have the same genealogical history.
I made the statement with the understanding that there are very highly admixed people groups as well as low admixture, the Ashkenazi were simply set as an example of a low admixed, bottlenecked population group. So it could be assumed then by the literature that this group had a lower speed of adaptation. This is what I simply said and nothing was implied in that. I also mentioned Han Chinese and Roma, as well as Native American. Currently there are only four accepted mtDNA haplotypes for Native Americans.
I wanted to remain with T and T2b for now.
From NCBI
This analysis shows that the putative secondary/intermediate LHON mutations 4216, 4917, 13708, 15257, and 15812 are ancient polymorphisms, are associated in specific combinations, and define two common Caucasoid-specific haplotype groupings (haplogroups J and T). On the contrary, the same analysis shows that the primary mutations 11778, 3460, and 14484 are recent and are due to multiple mutational events. However, phylogenetic analysis also reveals a different evolutionary pattern for the three primary mutations. The 3460 mutations are distributed randomly along the phylogenetic trees, without any preferential association with the nine haplogroups (H, I, J, K, T, U, V, W, and X) that characterize European populations, whereas the 11778 and 14484 mutations show a strong preferential association with haplogroup J. This finding suggests that one ancient combination of haplogroup J-specific mutations increases both the penetrance of the two primary mutations 11778 and 14484 and the risk of disease expression.
What does it mean, different evolutionary pattern for the three primary mutations? There are recent, and yet there is also ancient mutations, in an evolutionary sense, meaning that J is unique because there are specific mutations. Something is going on with the women.
OK J and T have no intermediates, but it shows that J and T both arose in the Levant.
This is my ancestresses lineage, so I feel I should be able to discuss this.
How does T2b get into Europe, before T2b arose?
T2b is indigenous to the Levant. While it says that
Our analysis confirms that haplogroups J and T and their major subclades (J1 and J2, T1 and T2) most likely arose in the Near East between the time of first settlement by modern humans and the LGM
OK, as it says here, they were not the AMH, but they come from a more ancient population.
It seems plausible to regard JT and U as belonging to members of the same early human group, ancestral to both Near Easterners and Europeans.
They arose at the same time R did, in the Levant, so R can not be ancestral if they arose at the same time. But their clade is indigenous
Indeed, the major T2 lineage, T2b, although displaying a star-like pattern dating to ∼10 ka ago, suggesting an expansion across Europe at the time of the early Neolithic period, may well have arisen indigenously within Europe from a T2 ancestor.
OK, what have we got going on here? That means that T2b is an indigenous European population, and that it was not bottlenecked, meaning that it had a different and accelerated evolutionary process. Therefore, not all populations of human groups can evolve at the same rate and speed, that means some populations reach speciation before others.
Would this not be true? But as genetics for evolution have been based primarily before on male individuals within the Homo Species.
It was recognized at the outset that mtDNA was strictly a marker for historical processes in females; should male and female history differ in a species, then this marker would not reflect the history of the species as a whole but that of the female portion.
TBC...