Geographical origin tally

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After getting some much needed rest, I now feel prepared to start the gradual process of sorting out what the studies in this article say about R1a origins, as well as clearing out the unreliable sources (such as blogs or tweets) in the article and general tidying.

I would also like to acknowledge my mis-characterization of the studies on 21:16 16 July 2023. I implied with this comment that most of the studies say the haplogroup originated in West Asia. As I will show below by compiling quotes from all of the studies, that was incorrect. I also hinted that we should specify that Wells (2001) was talking about R1a1, when the article already does. These errors might reflect my insufficent sleeing patterns and general laziness; at least that is what I am hoping for.

I will create sub-sections below tallying the studies for their proposed geographical origin of R1a.

Eastern Europe

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I will start this section off by saying is that there is a problematic statement in the "R1a origins" section that reads:

The ancient DNA record has shown the first R1a during the Mesolithic in Eastern Hunter-Gatherers (from Eastern Europe),[5][6] and the earliest case of R* among Upper Paleolithic Ancient North Eurasians,[7] from which the Eastern Hunter-Gatherers predominantly derive their ancestry.[8]

Haak, et al. (2015) ([6]) do mention the mesolithic R1a individual from Karelia, who they describe as the "oldest known" R1a specimen found to date, but not "the first". And yet they also acknowledge that the modern R1a was brought to Europe from the East and that Karelia did not belong to the derived lineage M417 within R1a.

These statements, while interesting and notable, don't explicitly support an Eastern European origin. They just note that mesolithic hunter gatherers had R1a and that a Karelian HG is the oldest sample of R1a yet identifed. Saag, et al. (2016) also suggest that it may have been a common haplogroup among EHG.

There is seemingly one citation in the body that does directly support an Eastern European origin: Semino, et al. (2000), who do say on page 1156:

... haplotypes Eu18 and Eu19 as signaatures of expansions from isolated population nuclei in the Iberian peninsula and the present Ukraine, following the Last Glacial Maximum (LGM). In fact, during this glacial period (20,000 to 13,000 years ago), human groups were forced to vacate Central Europe, with the exception of a refuge in the northern Balkans (16). Similar discrete patterns of the flora and fauna in Europe have been attributed to glaciation-modulated isolation followed by dispersal from climatic sanctuaries (18). This scenario is also supported by the finding that the maximum variation for microsatellites linked to Eu19 is found in Ukraine (19).

This beings my tally of studies supporting an Eastern European origin for haplogroup R1a to a grand total of 1. If anyone has more studies that support an Eastern European origin of R1a, go ahead and cite them, but until then I see no rationale for listing it as the first (and therefore, most supported, according to convention) location in the infobox. - Hunan201p (talk) 08:23, 19 July 2023 (UTC)Reply

@Hunan201p: Should we rearrange Possible place of origin paramter? And what would be the order? - Fylindfotberserk (talk) 09:56, 2 November 2023 (UTC)Reply
Hunan201p I think it would be more interesting to consider how many studies think R1a entered Europe from the east (via eastern europe). I think that by tallying to come to a conclusion we risk WP:SYNTH because in reality there is not much consensus about where R1a originated apart from somewhere between Europe and India.--Andrew Lancaster (talk) 10:48, 2 November 2023 (UTC)Reply
@Fylindfotberserk and Andrew Lancaster: thanks for your comments, sorry it has taken so long for me to respond. Running short on time these days. I totally agree with Andrew Lancaster that it would be original research to tally the sources to re-arrange the order in the infobox. That's why I feel better about giving up on that task, but also why I don't have much of an answer for Fylindfotberserk. I also concur with Andrew's observation that there doesn't appear to be a consensus as to where R1a originated. I will add more if I can find the time. Please press ahead if you've got a plan. - Hunan201p (talk) 11:43, 7 November 2023 (UTC)Reply
@Hunan201p and Andrew Lancaster: Possibly the reason why it was "Eurasia" for years in the "|Possible place of origin= parameter" before some newb editor replaced it with various regions . I wouldn't have a problem if we revert back to it and/or use some arrangement like this → "[[Haplogroup_R1a#Origins|see here]]" for the parameter. - Fylindfotberserk (talk) 12:18, 7 November 2023 (UTC)Reply
There will inevitably be editors who want to narrow it down further, but Eurasia is at least difficult for anyone to get upset about. Another source-based option is a list "x, y or z", or something like "proposals are mainly in the area stretching from x to y" although even that is difficult in this case?--Andrew Lancaster (talk) 12:55, 7 November 2023 (UTC)Reply
Good idea, folks! I'll start with Andrew's proposal and invite him to do the second when he finds the time. Hunan201p (talk) 00:46, 16 November 2023 (UTC)Reply

South Asia

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@Plumeater2: "South Asia is the preferred terminology. Pinging Fowler&fowler and RegentsPark for input. Joshua Jonathan - Let's talk! 09:18, 2 November 2023 (UTC)Reply

"Opinion piece from a newspaper"

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Regarding this revert diff, edit-summary

It doesn't explain the relationship between older TMRCA datings and high populations, nor can we accept an opinion piece from a newspaper without any academic study supporting such extraordinary genetic claims.

and this revert diff, edit-summary

Blatant POV pushing using an opinion piece. Discrediting all the studies mentioned before it. If anyone else wants to investigate the sources they are free to do it. Thsi is my last revert.

Tony Joseph refers to recent research, qouting dr. Richards, co-author of "“A Genetic Chronology for the Indian Subcontinent Points to Heavily Sex-biased Dispersals,” who rejects the idea that Indian R1a is very diverse. Anyone with even superficial knowledge of DNA-research knows that this research confirms the introduction of Indo-European related R1a into India around 2000 BCE. Joshua Jonathan - Let's talk! 21:10, 15 July 2024 (UTC)Reply

No, it doesn't. And I don't understand how you can disregard TMRCA datings like they are nothing. Diversity may be impacted by population density, but the South Asian diversity confirmed by various genetic studies could not have just formed after 2000 BC. As I said on my Talk page, to each their own. Someone rejecting the idea does not discredit years of genetic studies. 103.95.83.27 (talk) 21:16, 15 July 2024 (UTC)Reply
@Joshua Jonathan and Austronesier: I believe, we are giving too much emphasis to Tony Joseph's article. He isn't a geneticist and certainly not a scholar in this field, which is obvious from some of the excerpts from his work. I suggest we use the research papers directly for whatever we are citing here, instead of quoting Joseph. - Fylindfotberserk (talk) 10:49, 16 July 2024 (UTC)Reply
He's referenced two times, plus an additional quote in a note to support the reference. In both cases he quotes Richards, a geneticist. That's not "too much emphasis," I think. Joshua Jonathan - Let's talk! 11:49, 16 July 2024 (UTC)Reply
@Joshua Jonathan: Why not quote Richard and his paper directly? This person (Joseph) isn't a scholar and not qualified in this topic area, Indian media is politically driven, there are multiple factions in the media, especially when it comes to these historical topics. You'll find many articles supporting OIT as well. Don't need to use news articles and opinion pieces when we can diretly use research papers, for the sake of balance. - Fylindfotberserk (talk) 12:02, 16 July 2024 (UTC)Reply
Yes, and also inline citations from the study should be provided to support this extraordinary statement. These citations must include information about BOTH STR diversity and TMRCA datings, as both are being targeted here. No original research or synthesis by any 'Wikipedia scholar' should be tolerated. And even if we are able to find those inline citations( which i was unable to find), proper attribution must be provided, especially considering that one study is attempting to disregard all the previous multiple studies conducted before it. 103.95.83.206 (talk) 12:42, 16 July 2024 (UTC)Reply
So, you want to argue that R1a originated in India, and wasn't brought there with the Indo-Aryan migrations? Is microsatellite diversity even still being used as an instrument? It seems to be outdated; the dates of those studies are quite telling. Joshua Jonathan - Let's talk! 13:22, 16 July 2024 (UTC)Reply
See, Joshua, no one is discarding the possibility of Indo-European migrations during the last phase of the Indus Valley Civilization. I also believe in a close relationship between the Aryan and Andronovo/Sintashta cultures. But the problem arises when editors try to conduct original research. What do you mean by "it's still a thing"? How do you think the origin of a haplogroup is decided? The only exception is this haplogroup (for obvious reasons) where we are arguing. And let's say it didn't originate in South Asia. However, the highest frequencies and most diversity of R1a in South Asia, along with the oldest TMRCA datings, indicate a long and complex history of human presence and migration in the region. The Indo-Aryan migrations likely involved multiple waves and significant interaction with existing populations, leading to the genetic patterns observed today. It’s not that simple that one small group came from Central Asia and changed the whole South Asian and Iranian genetics at this level. All we are asking is that if you are trying to negate all these studies, something better is required. Dont fall for biased indian newspapers (from both sides of political spectrum) 103.95.83.206 (talk) 14:13, 16 July 2024 (UTC)Reply

Regarding the highest frequencies and most diversity of R1a in South Asia, along with the oldest TMRCA datings, the research you cherish is outdated, and rejected by more recent research, such as Underhill et al. (2015) and Narasimhan et al. (2019), conducted with much better methods. Regarding biased indian newspapers, what you call 'an opinion piece' was published in the science-section of The Hindu. That Hindu nationalists have problems with appreciating scientific insights does not mean that their opponnts are suffering from the same deficiency. Joshua Jonathan - Let's talk! 16:00, 16 July 2024 (UTC)Reply

Yes, please cite "the research" with inline citations. Cite the better methods (what are those?). And provide attribution if it's only one study. The whole argument is about that. But its your old habit to divert the topic of debate. Even in the opinion piece, there is nothing about TMRCA dating. Only a vague statement about diversity, which I was unable to find in your "top-notch research." And what research rejected highest frequencies? I mean seriously, now you included frequency rejection too, lol? The thing is, it's pointless having any conversation with you. You are in complete denial. I understand. You have a set agenda and a worldview you can't seem to break down. I don't have time for this. If others are interested, they can engage with you. Otherwise, hey, it's Wikipedia. Most articles here need serious improvements, but I am not going to waste my time as it's full of editors like you. If others have no problem with your baseless extraordinary assertions, do what you wish. Who am I to stop you? Have a good day! 103.95.83.51 (talk) 16:19, 16 July 2024 (UTC)Reply
So anyone who goes against your opinion is a hindu nationalist? Nice. M out 103.95.83.51 (talk) 16:21, 16 July 2024 (UTC)Reply
Underhill et al. (2015) is already exyensively mentioned; I've added Narasimhan et al. (2018) to the India-subsection. You have a point about the genetic diversity and multiple waves; I've adjusted some text in line with that diff. Joshua Jonathan - Let's talk! 16:28, 16 July 2024 (UTC)Reply
Again, don't reply to me. Do what you wish. Change the article however you want. Make the frequency of R1a in Brahmins from 72% to 27%, in Khatris from 65% to 15%, etc., citing the Hindu article or whatever source you have. Make the STR diversity of South Asia lower than that of Europe, West Asia, and Central Asia. Adjust the TMRCA datings in South Asia to 2,000 years from more than 15,000 years. I don't care. I made my points above. Provide inline citations for your statement, which I initially marked as "failed verification," that attempt to reject whatever we know about South Asian populations. And now, don't bother me. I am done. 103.95.83.51 (talk) 16:37, 16 July 2024 (UTC)Reply
(edit conflict)@Joshua Jonathan: As I said, there are many factions in the Indian media, the anti-Hindu nationalist lobby is as much problematic as the other. Hence, it would be wise to use research papers directly instead of quoting lay-people from Indian media, supporting a certain narrative. Don't we already have links to Underhill, Narasimhan and Silva? We do not need quote from Joseph's article, who doesn't seem to know the obvious that females can't have R1a. - Fylindfotberserk (talk) 16:36, 16 July 2024 (UTC)Reply
Jospeh quotes Richards, a published genetic scientist; Richard questions the idea, based on microsatellite variations, that R1a originated in India; it seems to me that this is relevant, precisely because of the reference Hindu nationalists make to these outdated studies. Joshua Jonathan - Let's talk! 16:45, 16 July 2024 (UTC)Reply
@Joshua Jonathan: I'm not questioning the points raised by Richard, but the use of Joseph's work who isn't a scholar of the subject. Why can't we use Richard work directly. Why do we have to make Wikipedia a vehicle for Anti-Hindu-nationalist agenda if we are vehemently against Hindu-nationalist agenda? For the sake of balance, we shouldn't be entertaining both. Don;t we have Richard's work available? If not Underhill and Narasimhan will do. - Fylindfotberserk (talk) 16:58, 16 July 2024 (UTC)Reply
he's co-author of Da Silva et al. (2017). Joshua Jonathan - Let's talk! 17:06, 16 July 2024 (UTC)Reply
@Joshua Jonathan: I'm aware that Martin B. Richards is a co-author of Da Silva et al. (2017). But not journo Tony Joseph. Let's replace this with Martin B. Richard's work in which he said − "the idea that R1a is very diverse in India, which was largely based on fuzzy microsatellite data, has been laid to rest”. - Fylindfotberserk (talk) 17:15, 16 July 2024 (UTC)Reply

Suggestions? Joshua Jonathan - Let's talk! 18:14, 16 July 2024 (UTC)Reply

@Joshua Jonathan: Is Martin B. Richards paper where he said, "the idea that R1a is very diverse in India, which was largely based on fuzzy microsatellite data, has been laid to rest” available in the internet, do we have a link? - Fylindfotberserk (talk) 18:31, 16 July 2024 (UTC)Reply
It's a reply from Richards to Joseph in an email-exchange, in the context of their 2017 publication. Joshua Jonathan - Let's talk! 19:04, 16 July 2024 (UTC)Reply
I'm with Fyl here. Not for the sake of balance, but for the sake of science. It's pretty simple. Two days ago, we have rejected the addition of a small piece of text in Indus Valley Civilisation based on promotional interviews given by no one less than David Reich for launching the publication of Shinde et al. (2019). Some editor was so determined on adding (and re-re-re-adding) the piece that they got blocked. I rejected the addition with a plain rationale: WP:SCHOLARSHIP. Unless you want to cover ideological meta-debates surrounding findings from population genetics (in which case press articles can be fine as sources), the only apt sources for a scientific topic like this one are peer-reviewed academic sources, ideally secondary sources (like Fox (2022) which is a good addition here), or if we feel we can't do without primary sources, then at least widely cited primary sources with widely supported findings. So no, please don't cite news media for genetic research, whether they interview Reich or Richards. If the things scholars say in an interview are indeed relevant and supported by their research, we should be able to find sources that pass WP:SCHOLARSHIP in suppport of the very things they say in interviews. –Austronesier (talk) 19:34, 16 July 2024 (UTC)Reply
@Joshua Jonathan: Also this one - "According to Martin P. Richards, co-author of Silva et al. (2017), the prevalence of R1a in India was "very powerful evidence for a substantial Bronze Age migration from central Asia that most likely brought Indo-European speakers to India."[19][note 2]" - should be removed.
Have a look at this - "offering proof that R1a arrived in India with multiple waves of migration, including Iranian hunter-gatherers and the Indo-Aryans." - don't see any of the sources associating this hg with Iranian HGs. - Fylindfotberserk (talk) 20:52, 16 July 2024 (UTC)Reply
Sorry, I couldn't resist coming back after reading "from Richards to Joseph in an email exchange"—I literally laughed at this. This should not be the standard of a high-level editor. It is a clear example of how ideological biases can make a usually rational and well-read person like Joshua no better than the people he criticizes day and night. Joshua has now removed the objectionable sentence for which I asked for verification, which is commendable ( i know its never easy to swallow your pride- i am very similar);
Although there is still some bias, such as using a random phylogenetic reconstruction (which should not be used) to claim that more recent research has questioned older studies, there's no need to state 'older' studies "from this year to this"—they were not done thousands of years ago. Also, multiple waves of migration do not necessarily mean that migration only started after 2000 BC, which we are using as support for the conclusion (considering older TMRCA datings). However, these are comparatively smaller issues that may be addressed in the future by someone else (I am not touching the article now).
Overall, what remains is not as biased as the previous statement, which didn't even make any sense. It was not only illogical but also impossible, considering the number of genetic studies we have that we can also cite—with inline citations. It's also not OK to convey the message, directly or indirectly, that all previous researchers were maybe lying because maybe they were all Hindu nationalists. Regards, 103.95.83.148 (talk) 20:54, 16 July 2024 (UTC)Reply

Paper: Decoding Quraysh Origins

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Hi @InfernoHues,

I have restored the content with the paper now properly cited:

Zenodo is not on the blacklist, and the paper is also indexed on OpenAIRE https://www.unesco.org/en/open-science/inclusive-science/openaire-portal here: https://explore.openaire.eu/search/result?pid=10.5281/zenodo.20078805. The same content is also presented on grokipedia.com here: https://grokipedia.com/page/Sayyid

The earlier removal was because the first version used a clear LLM-generated draft. This version uses the formal published Zenodo paper.

Would you mind taking another look? I'm happy to discuss whether this meets WP:RS / WP:PREPRINTS for the specific claims.

Thanks, ~2026-34474-45 (talk) 22:37, 10 June 2026 (UTC)Reply

I've responded on Talk:Sayyid, so we don't have identical discussions going on. InfernoHues (talk) 23:28, 10 June 2026 (UTC)Reply
Hi @InfernoHues,
Thank you for your reply and for explaining your concerns.
I am a separate editor who believes the paper contains useful information.
Regarding the source:
  • Yes, I understand it is a preprint on Zenodo and not a peer-reviewed journal article.
  • However, Zenodo is not blacklisted, and the paper is indexed on OpenAIRE.
  • I have made sure the article text reflects the content of the published paper (doi:10.5281/zenodo.20078805).
Would you be okay with keeping the material with proper attribution and inline citation, possibly with a note that it is a preprint? Or do you think this topic needs a peer-reviewed journal source before it can be included?
I'm happy to adjust the wording or provide additional context if needed. Looking forward to your thoughts.
Thanks, ~2026-34474-45 (talk) 23:53, 10 June 2026 (UTC)Reply
Please keep the conversation on one page. InfernoHues (talk) 00:04, 11 June 2026 (UTC)Reply
Hi @InfernoHues,
Zenodo is not on the blacklist and is an accepted academic repository. I would like to present the following sources regarding the most common paternal lineage among self-identified Syeds:
These sources indicate that R1a (particularly subclades such as R-Y6) is the most common Y-DNA lineage among many self-identified Syeds.
Thanks, ~2026-34474-45 (talk) 00:59, 11 June 2026 (UTC)Reply
None of those are reliable sources (WP:RS). InfernoHues (talk) 01:28, 11 June 2026 (UTC)Reply
Hi @InfernoHues,
All the sources I mentioned are included and discussed in the Decoding Quraysh Origins paper. They indicate that R1a is the most common Y-DNA lineage among many self-identified Syeds in South Asia.
Relevant studies:
These are also summarized on the last page of this document:
https://archive.org/download/SyedR1aGlance-BayesianAnalysis/1.SyedR1aGlance.pdf
Given the data from South Asia, it is difficult to ignore that a majority of self-identified Syeds belong to R1a.
Thanks, ~2026-34474-45 (talk) 01:50, 11 June 2026 (UTC)Reply
You'll need to find a reliable source for that claim. The Decoding Quraysh Origins "paper" is not one. If you want to cite a different reliable source, that's all fine with me. InfernoHues (talk) 01:59, 11 June 2026 (UTC)Reply
Hi @InfernoHues,
The Decoding Quraysh Origins paper is based on several reliable sources. It provides a detailed explanation showing that many self-identified Syeds belong to an unbranched Y6 (a subclade of R1a).
No single peer-reviewed source has yet combined all of this information together. Therefore, we have to work with the currently available source until better one is published.
The reliable sources include:
Thanks, ~2026-34474-45 (talk) 02:23, 11 June 2026 (UTC)Reply
"Therefore, we have to work with the currently available source until better one is published." - No we don't. Please see WP:Reliable sources. InfernoHues (talk) 02:40, 11 June 2026 (UTC)Reply
Hi @InfernoHues,
I find it a bit surprising that the Decoding Quraysh Origins paper has been accepted and indexed on platforms such as Archive, Zenodo, OpenAIRE and Grokipedia, yet it is still not considered suitable here.
If you have a moment, could you please take a look at the paper? We have reviewed it carefully ourselves along with feedback from multiple AIs, and we did not find any major issues with the work.
For context on how AI-assisted research is increasingly being viewed in academia, you may find this recent New York Times article interesting:
https://www.nytimes.com/2026/06/08/science/ai-scoop-young-mathematicians.html
I would appreciate your thoughts.
Thanks, ~2026-34474-45 (talk) 03:19, 11 June 2026 (UTC)Reply
Those platforms have nothing to do with the reliable sources guideline which I have already linked several times. My personal opinion does not matter, the guideline does. InfernoHues (talk) 03:24, 11 June 2026 (UTC)Reply
Hi @InfernoHues,
Zenodo (which is not on the blacklist) reviewed the Decoding Quraysh Origins paper and officially accepted it. The author received a formal acceptance email from Zenodo.
Thanks, ~2026-34474-45 (talk) 03:33, 11 June 2026 (UTC)Reply
Yet again, please read WP:ZENODO and WP:Reliable sources. We're going in circles here. InfernoHues (talk) 03:36, 11 June 2026 (UTC)Reply
Also, how do you know the author received an email? InfernoHues (talk) 03:37, 11 June 2026 (UTC)Reply
Hi @InfernoHues,
Zenodo's status is clearly listed as "No consensus" and not "Blacklisted". Please read the relevant pages carefully:
Regarding the acceptance email: the author has publicly stated on his social account that he received an official acceptance email from Zenodo.
Thanks, ~2026-34474-45 (talk) 03:48, 11 June 2026 (UTC)Reply
I'm not going to repeat myself for the umpteenth time. Please don't add the text back into the article. InfernoHues (talk) 03:50, 11 June 2026 (UTC)Reply
Hi @InfernoHues,
Wikipedia decisions are not made by a single person.
Here is the Zenodo acceptance email:
https://x.com/SheikhAbrahams_/status/2064919437837234554
https://pbs.twimg.com/media/HKgRRD_XcAAZCnG?format=jpg&name=large
Thanks, ~2026-34474-45 (talk) 04:02, 11 June 2026 (UTC)Reply
That's irrelevant to adding the line or not. Feel free to follow other WP:Dispute resolution steps to see what other editors think. InfernoHues (talk) 04:10, 11 June 2026 (UTC)Reply

Should the "Decoding Quraysh Origins" preprint (Zenodo) be used as a source for claims about Syed Y-DNA?

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The following discussion is an archived record of a request for comment. Please do not modify it. No further edits should be made to this discussion. A summary of the conclusions reached follows.
Opener blocked for sockpuppetry. InfernoHues (talk) 03:20, 13 June 2026 (UTC)Reply

Should the preprint Decoding Quraysh Origins (Abrahams, 2026, Zenodo doi:10.5281/zenodo.20078805) and its associated supplementary materials be considered a reliable source for claims that R1a-Y6 is the most common paternal haplogroup among self-identified Syeds?

Background:

  • The paper compiles data from several studies (including Belle et al. 2010) and 23andMe surname statistics.
  • It concludes that many Syeds belong to an unbranched Y6 subclade of R1a.
  • One editor argues it is not a reliable source because it is a self-published preprint.
  • The other side argues that Zenodo is not blacklisted and the paper should be usable with attribution.

Question: Is this preprint acceptable as a source (with clear attribution as a preprint) for genetic claims about Syeds in the Haplogroup R1a and/or Sayyid articles?

~2026-34474-45 (talk) 04:19, 11 June 2026 (UTC)Reply

No - Not only does this "paper" not meet the reliable source policy, at the end it says that it was generated with an LLM. There's also a duplicate RfC at Talk:Sayyid. InfernoHues (talk) 04:26, 11 June 2026 (UTC)Reply
Hi @InfernoHues (and others),
I would like to summarize my position clearly in one place:
The Decoding Quraysh Origins paper (Zenodo, doi:10.5281/zenodo.20078805) was formally accepted by Zenodo and is indexed on OpenAIRE. It is not on the blacklist (its status is "No consensus"). The paper compiles data from several existing studies, including Belle et al. (2010), regional Khyber Pakhtunkhwa genetic papers, and 23andMe surname statistics. It argues that R1a-Y6 is the most common paternal lineage among many self-identified Syeds in South Asia.
I acknowledge that it is a preprint and that parts of it involved LLM assistance. However, the author states it was reviewed before final upload, and Zenodo sent an official acceptance email.
I understand concerns about reliability, but I believe the paper can be used with clear attribution as a preprint.
Since discussions are happening on both Talk:Sayyid and Talk:Haplogroup R1a, I suggest we continue in one place. I would appreciate input from other editors.
Thanks, ~2026-34474-45 (talk) 05:19, 11 June 2026 (UTC)Reply
Ai assistant usage is good for polishing if the content based on reliable sources and widely acceptable on various platforms and moreover published well ~2026-34452-66 (talk) 18:04, 11 June 2026 (UTC)Reply
I've terminated the identical discussion at Talk:Sayyid#Should the "Decoding Quraysh Origins" preprint (Zenodo) be used as a source for claims about Syed Y-DNA? per WP:MULTI. But really this should have been brought up at WP:RSN, but as a normal discussion, not as a full-blown thirty-day formal WP:RFC. --Redrose64 🌹 (talk) 19:44, 11 June 2026 (UTC)Reply
Hi @Redrose64,
Thank you for closing the duplicate discussion on Talk:Sayyid and for the advice.
I understand now that this type of question is better suited for the Reliable Sources Noticeboard (WP:RSN) as a regular discussion rather than a formal RfC. I will open a thread there shortly.
Thanks again for your help, ~2026-34537-99 (talk) 21:45, 11 June 2026 (UTC)Reply
You might want to explain why you think the WP:PREPRINT rules don't apply here. WhatamIdoing (talk) 06:00, 12 June 2026 (UTC)Reply
The discussion above is closed. Please do not modify it. Subsequent comments should be made on the appropriate discussion page. No further edits should be made to this discussion.