FamilyTreeDNA and WikiTree Collaboration – In Two Easy Steps!!

I’m thrilled to see that FamilyTreeDNA and WikiTree have joined genealogical forces!

FamilyTreeDNA  has announced a second option for tree connections for their customers – WikiTree. If you’ve been a blog subscriber for long, you know that I love WikiTree and use it almost daily.

A few months ago, FamilyTreeDNA obsoleted their own family trees and encouraged their customers to migrate their family trees to MyHeritage. Now there’s an additional option for FamilyTreeDNA customers.

This is NOT an either/or decision, because you can easily choose both. You can link to your MyHeritage tree, or you can link to your WikiTree profile, or both. I’m doing both because I want the maximum reach for my testing dollar!

Katy Rowe at FamilyTreeDNA  has done a wonderful job of providing examples of how to use the various WikiTree DNA features, here, in her blog article, so I’m not replowing that field.

I do want to show you how to implement the new WikiTree connection in two easy steps.

But first, let me tell you why I love WikiTree so much, and why you will too.

Why I Love WikiTree

Let me confess – in general, I don’t care for one-world-trees, but WikiTree is the exception because WikiTree has built a platform that incorporates a collaborative community.

I will always maintain my detailed genealogy information in my desktop computer program, and I will also maintain my trees at both Ancestry and MyHeritage, which are subscription sites that facilitate records searching. Both have different strengths and weaknesses, but WikiTree is free, and everyone can participate.

I think of WikiTree as an “ancestor information aggregator” or maybe a “data repository” that’s available to everyone.

People often ask, “How can I preserve my research for future generations?” and WikiTree is certainly an excellent answer.

Here’s the link to my profile at WikiTree so you can take a look.

https://www.wikitree.com/wiki/Estes-2153

Click on any image to enlarge

I’ve made this much of my profile information public, but just so you know, you’re in charge of what information is private and what is not by clicking on the little lock at the top right of your profile page.

You can see that there’s a lot of information available to help with just about everything WikiTree, including privacy selections.

On my profile, you might notice that I’m fairly active.

At right, I’ve entered the DNA tests that I’ve taken, except I need to update this to include both Ancestry and MyHeritage.

WikiTree shows other testers who have tested and may match people related to this ancestor, populating the information up and down the tree appropriately.

WikiTree also populates Y-DNA and mitochondrial DNA information up the tree to the appropriate ancestors. I can’t tell you how much I LOVE THIS!! As you know, I encourage everyone to “collect” the Y-DNA and mtDNA haplogroups of their ancestors because they not only are genealogically relevant, but haplogroups also reach back before surnames where no other tests can reach – and let’s face it, you don’t know what you don’t know.

Here’s the DNA section of my mother’s profile, with my mtDNA test showing for her, because I’m her direct matrilineal descendant and received my mitochondrial DNA from her.

In the autosomal section, you’ll find other people who might share some of her DNA, and where they tested.

Wait! What??? There’s a new person, Helene, that I don’t know. I need to run right over and take a look at Helene’s profile. Because I can just click on these tester’s name to see their tree, I immediately know how they are related to my mom.

My Tree

You can also see my tree easily from my profile by clicking on the “Ancestors” tab.

And you know what, I didn’t have to build the entire thing. I only had to build the part that is unique to me, until I connected with a WikiTree profile that already exists.

Step 1 – Getting Started at WikiTree

WikiTree has provided a series of instructional pages to help you get started, here.

This article tells you very specifically how to begin to set up your profile and find your ancestors.

You can approach this one of two ways:

  • You can search to see if your grandparents or great grandparents are already at WikiTree. Mine were, so all I had to do was add the profiles that don’t already exist down to me.
  • Or, you can upload a 5000-person or less GEDCOM file and use the GEDCOMpare report which shows you which profiles already in WikiTree might be your ancestors.

My recommendation is to try searching for your grandparents and great-grandparents first because you only need to provide information until you connect with a profile that already exists.

And yes, after you get started and “settled in,” you absolutely will want to review the profiles of each ancestor, add sourced information, and make corrections, if needed. If there’s a conflict, the comments serve as a discussion area, there’s a profile manager, and if needed, there are moderators with specialties to help. That’s what WikiTree is all about – jointly beneficial collaboration.

Once you’ve set up your profile at WikiTree, you just provide a link at FamilyTreeDNA to your WikiTree profile. That’s it. Seriously, just this easy.

Step 2 – Entering Your WikiTree ID at FamilyTreeDNA

Sign on to your account at FamilyTreeDNA.

On your personal page, in the upper right-hand corner, click the down arrow, then “Account Settings.”

Then select “Genealogy” and “Family Tree” and scroll to the WikiTree section at the bottom.

You’ll just copy and paste your WikiTree profile ID.

You can find your WikiTree profile ID in two places. The URL is shown at the top of your profile page, or you can click the link button, which copies the link for you. Be sure you’re on the profile of the page you want to enter into the account at FamilyTreeDNA . I manage several accounts, so don’t forget whose profile you’re viewing.

Back at FamilyTreeDNA, just paste your WikiTree profile ID link into that field at the bottom of the page, and click “Save.” That’s it!!

It takes effect immediately, so now your matches can choose to view any tree you have made available at FamilyTreeDNA.

Viewing WikiTree Trees of Your Matches

I’m signing on to my Mom’s account at FamilyTreeDNA, which I manage, to show you how WikiTree availability appears to your matches.

On my Mom’s match with me, if you click on the little tree icon at far right, you’ll see that you can now select from both trees that I have available, MyHeritage and WikiTree.

If you click on WikiTree, you will see my profile page. Just click on the “Ancestors” tab to view my tree!

That’s it.

I’m signing in right now to every FamilyTreeDNA kit that I manage and adding their WikiTree profile link. This is SO EASY, and FamilyTreeDNA says that more collaborative features are on the way!

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Mitotree Q&A for Everyone

I recently presented Mitotree Webinar – What It Is, How We Did It, and What Mitotree Means to You at Legacy Family Tree Webinars. It’s still free to view through June 13th, and after that, it’s available in the webinar library with a subscription. The 31-page syllabus is also a subscription feature.

Thank you to all 1000+ of you who attended and everyone else who has since watched the webinar – or will now.

We had a limited amount of time for Q&A at the end, so Geoff, our host, was kind enough to send me the list of questions from the Chat, and I’m doing the Q&A here. But keep in mind, please, that I’m assuming when I answer that you’ve watched the webinar or are familiar with how the new Mitotree and tools work.

That said, I think this Q&A can help everyone who is interested in mitochondrial DNA. Your genealogy gift from your mother and her female lineage.

Just a quick reminder that the mitochondrial DNA test tracks your direct matrilineal line only, meaning your mother’s mother’s mother’s line on up your tree until you run out of mothers. Of course, our goal is always to break through that brick wall.

This is a wonderful opportunity, because, unlike autosomal DNA, mitochondrial DNA is not admixed with the DNA of the other parent, so it’s a straight line look back directly up your mother’s female line.

Aha Moment!

Geoff said at the end that he had an aha moment during the webinar. Both males and females have mitochondrial DNA inherited from their mother, so we think of testing our own – but forget to obtain the mitochondrial DNA of our father. Testing your father’s mitochondrial DNA means obtaining your paternal grandmother’s mitochondrial DNA, so test your father to learn about his mother’s maternal line.

And it’s Father’s Day shortly.

Q&A

I’ve combined and summarized similar questions to make this short and sweet. Well, as short and sweet as I can make anything!

  • Can I benefit from Discover even if I don’t have a full sequence test?

You can benefit from the free FamilyTreeDNA Discover tool with any haplogroup, even a partial haplogroup. Be sure to click the down arrow and select mtDNA before entering the haplogroup if you’re using the public version.

However, to gain the most advantage from your test results and Discover, and to receive your closest matches, you need the full sequence test, called the mtFull, which you can purchase here. If you took one of the lower-level “Plus” tests, years ago, click here to sign in and upgrade or check your account to see if you have the full sequence test.

  • What benefits do I receive if I click through to Discover from my account versus using the public version of Discover?

Click any image to enlarge

If you click through to Discover directly from your FamilyTreeDNA account, you will receive features and additional information that are not available in the free, public version of Discover.

You’ll receive additional Notable Connections and up to 30 Ancient Connections based on how many are available and relevant for you.

You’ll also be able to view the Match Time tree, showing your matches, their earliest known ancestors, and where they fit in your haplogroup and haplotype cluster. In this example, two EKAs hinted at a common lineage, which turned out to be accurate after I did some digging.

I think the Match Time Tree is indispensable – the best thing since sliced bread!

The Scientific Details report is also customized for you with your Haplotype Cluster and your private variants.

  • Will a child and their mother always have the same haplogroup?

Yes, but if one of them has a mutation that the other doesn’t, or a heteroplasmy, they may be in a different haplotype cluster.

Also, they both need to have taken the full sequence test. Otherwise, the one who did not take the full sequence test will only have a partial haplogroup until they upgrade.

We will talk more about edge cases in Q&A on down the list.

Great question. Sign in to your account.

In the Maternal Line Ancestry section, which is mitochondrial DNA, check to see if both the Plus and Full boxes are pink. If so, you have taken both and you’ll have a new Mitotree haplogroup and haplotype cluster.

If the “Full” box is grey, you can either click there or at the top where it says “Add Ons and Upgrades” to upgrade to the full sequence test.

  • Why is it called the Million Mito Project? What were you counting?

When we first launched the project, we hoped for a million full sequence samples to build the initial tree. After removing duplicates, such as parent/child, partial sequence samples such as HVR1/2, unreliable samples from PhyloTree, and including FamilyTreeDNA  testers and academic samples, we had between one-third and half a million samples when we launched. The Mitotree and Discover are growing with new testers and groups of samples from archaeological studies, academic samples, and other publicly available resources, following quality analysis, of course.

  • Is there a way to confirm that I submitted an mtDNA to the Mito Tree project? I think I submitted my mom’s when you first started, but my husband recently tested, and I don’t remember if we opted him in at that time.

The science team at FamilyTreeDNA  is using all of the full sequence tests in the construction of the Mitotree, so you don’t need to do anything special.

  • Do or can haplotype F numbers (haplotype clusters) ever become haplogroups?

The answer is maybe. (I know – I’m sorry!)

If you have private variants in addition to your haplotype cluster, then yes, those are haplogroup seeds.

This is my result and I have no additional private variants left to use.

If you don’t have any private variants, or mutations, left over, then no, you won’t receive a new haplogroup for this reason. However, if for some reason the haplogroup splits upstream, you might receive a new haplogroup in the future due to that split.

In addition to the webinar, I wrote about haplotype clusters in the article, Mitochondrial DNA: What is a Haplotype Cluster and How Do I Find and Use Mine?

  • How can mitochondrial DNA and the Mitotree be useful for breaking down genealogy in various parts of the world?

There are two aspects to mitochondrial DNA testing.

The first is to connect genealogically, if possible. To do that, you’ll be paying attention to your matches EKAs (earliest known ancestors), their trees, and their locations. You may well need to do some genealogy digging and build out some trees for others.

The second aspect is to learn more about that lineage before you can connect genealogically. Where did they come from? Do they share a haplogroup with any Ancient Connections, and what cultures do they share? Where did they come from most recently in the world, and where do the breadcrumbs back in time lead?

I wrote about this in the article, New Mitotree Haplogroups and How to Utilize Them for Genealogy.

Sometimes, DNA testing of any type is simply a waiting game until the right person tests and matches you. That’s one reason it bothers me so much to see people “not recommend” mitochondrial DNA testing. We all need more testers so we can have more matches.

  • When will Globetrekker for mtDNA be available?

I don’t know and neither does the team. The Mitotree is still being refined. For example, we are adding thousands of samples to the tree right now from multiple locations around the world. I probably wouldn’t expect Globetrekker until the tree is officially out of Beta, and no, I don’t know when that will happen either. It’s difficult to know when you’re going to be “finished” with something that has never been done before.

While it’s not Globetrekker, you do have the Matches Map to work with, and the Migration Map in Discover, which also shows the locations of your Ancient Connections.

  • During the webinar, Roberta mentioned that her ancestor is German, but she discovered her ancestors were Scandinavian. Can you expand about the “event” that explained this unexpected discovery.

In my case, the church records for the tiny village where my ancestor lived in Germany begin right after the 30 Years’ War, which was incredibly destructive. Looking at Swedish troop movements in Germany, the army of Gustavus Adolphus of Sweden marched through the region with more than 18,000 soldiers. Women accompanied the baggage trains, providing essential, supportive roles and services to the soldiers and military campaign. I’ll never know positively, of course, but given that the majority of my full sequence matches are in Scandinavia, mostly Sweden, and not in Germany, it’s a reasonable hypothesis.

People often receive surprises in their results, and the history of the region plays a big role in the stories of our ancestors.

You don’t know what you don’t know, until you test and follow the paths ahd hints revealed.

  • Why do I have fewer matches in the HVR2 region than the HVR1 region?

Think of the mitochondria as a clock face.

The older (now obsolete) HVR1 test tested about 1000 locations, from about 11-noon and the HVR2/3 region tested another 1000 locations, from about noon-1 PM. The full sequence test tests the full 16,569 locations of the entire mitochondria.

Each level has its own match threshold. So, if you have one mutation at either the HVR1 or HVR2/3 level, combined, you are not considered a match. For example, you can match 10 people at the HVR1 level, and have a mutation in the HVR2 level that 4 people don’t share, so you’ll only match 6 people at the HVR2 level.

If you have one mutation in the HVR1 region, you won’t match anyone in either the HVR1 or HVR1/HVR2 regions.

At the full sequence level, you can have three mutation differences (GD 3) and still be considered a match.

So, the short answer is that you probably have a mutation that some of your matches at the HVR2 level don’t have.

In addition to matches on your Matches page, you will (probably) have haplogroup matches that aren’t on your match list, so check Discover for those.

  • I have HVR1/HVR2 matches, but none at the full sequence level. Why?

It’s possible that none of your matches have tested at that level.

You have no mutations in the HVR1/2 region, or you would not be a match. If your HVR1/2 matches have tested at the full sequence level, then you have more than 3 mutations difference in the coding region.

  • Why do I match people at the full sequence level but not HVR1/2?

The match threshold at the HVR1/2 level is 1, so if you have one mismatch, you’re not listed as a match. However, at the full sequence level, the GD (genetic distance) is 3 mismatches. This tells me you have a mismatch in the HVR1 region, which also precludes HVR2 matching, but less than 4 mutations total. Click on the little “i” button above each match level on the matches page.

  • Why don’t all of my matches show on the Match Time Tree?

Only full sequence matches can show on the Match Time Tree, because they are the only testers who can receive a full haplogroup.

  • How does a heteroplasmy interfere with mtDNA research?

Heteroplasmies, where someone carries two different nucleotides at the same location in different mitochondrial in their body, are both extremely fascinating and equally as frustrating.

Heteroplasmies can interfere with your matching because you might have a T nucleotide in a specific location, which matches the reference model, so no mutation – like 16362T. Your mother might have a C in that location, so T16362C, which is a mutation from T to C. Your aunt or sister might have both a T and a C, which means she is shown with letter Y, so 16362Y, which means she has more than 20% of both. All three of you probably have some of each, but it’s not “counted” as a heteroplasmy unless it’s over 20%.

The challenge is how to match these people with these different values accurately, and how heteroplasmies should “count” for matching.

I wrote about this in the article What is a Heteroplasmy and Why Do I Care?

Bottom line is this – if you are “by yourself” and have no matches, or you don’t match known relatives exactly, suspect a heteroplasmy. If you ask yourself, “What the heck is going on?” – rule out a heteroplasmy. Check out my article and this heteroplasmy article in the FamilyTreeDNA help center.

  • Someone asked about the X chromosome and may have been confusing it with mitochondrial DNA. The X chromosome is not the same as mitochondrial DNA.

The confusion stems from the fact that both are associated with inheritance from the maternal line. Everyone inherits their mitochondrial DNA from their mother. Men inherit their X chromosome ONLY from their mother, because their father gives them a Y chromosome, which makes them a male. Females inherit an X chromosome from both parents. And yes, there are medical exceptions, but those are unusual.

I wrote about this in the article, X Matching and Mitochondrial DNA is Not the Same Thing.

  • How do you determine the location of the last mutation? A tester and their aunt are from one country, and another man in the same haplogroup is from another country, but he has tested only the HVR1/HVR2 level.

There are really two answers here.

First, you can’t really compare your full sequence new Mitotree haplogroup with a partial haplogroup based on only the HVR1/2 test. Chances are very good that if he upgraded to a full sequence test, he would receive a more complete haplogroup, and one that might be near the tester’s haplogroup, but perhaps not the same.

For example, my full sequence haplogroup is J1c2f. I have matches with people who only tested at the HVR1/HVR2 level, but they can only be predicted to haplogroup J, with no subgroup, because they are missing about 14,000 locations that are included in the full sequence test.

Using the Discover Compare feature, comparing haplogroup J to J1c2f clearly shows that the mutations that define haplogroup J1c2f happened long after the mutation(s) that define haplogroup J.

You can use other Discover tools such as the Match Time Tree (if you click through from your account), the Time Tree, the Ancestral Path and the Classic Tree to see when the various haplogroups were born.

  • My mother took the full sequence test in 2016, so should I look for an upgrade now? She is deceased so can’t retest.

First, I’m sorry for your loss, but so glad you have her DNA tests.

The good news is that you ordered the full sequence right away, so you don’t need to worry about an upgrade failing later. In this case, there is no upgrade because the full sequence tests all 16,569 locations.

Additionally, had you needed an upgrade, or wanted to do a Family Finder test, for example, FamilyTreeDNA stores the DNA vials for future testing, so you could potentially run additional tests.

And lastly, since we’re talking mitochondrial DNA, which you inherit from your mother with no admixture from your father, your mtDNA should match hers exactly, so you could test in proxy for her, had she not already tested.

  • Has anything changed in Native American haplogroups?

Absolutely. About 75% of testers received a new haplogroup and that includes people with Native American matrilineal ancestors.

For example, my Native ancestor was haplogroup A2f1a, formed about 50 CE and is now A2f1a4-12092, formed about 1600 CE, so has moved 2 branches down the tree and about 1500 years closer. My ancestor was born about 1683. Her descendant has 58 full sequence matches, 22 in the same haplogroup, and 16 people in their haplotype cluster.

I’m so excited about this, because it helps provide clarity about her ancestors and where they were before she entered my genealogy by marrying a French settler.

  • Are mtDNA mutations the same or similar to autosomal SNPs?

A SNP is a single nucleotide polymorphism, which means a single variation in a specific location. So yes, a mutation is a change in a nucleotide at a genetic location in Y-DNA, autosomal DNA, or mitochondrial DNA.

  • Can we filter or sort our matches by haplotype on our match page?

Not yet. Generally, your closest matches appear at or near the top of your match list. Of course, you can use the Discover Match Time Tree and you can download your matches in a CSV file. (Instructions are further down in Q&A.)

  • Is there a way to make it more obvious that the EKA should be in their matrilineal line? There are so many men as EKAs!

So frustrating. The verbiage has been changed and maybe needs to be revised again, but of course, that doesn’t help with the people who have already entered males. We know males aren’t the source of mitochondrial DNA.

When I see males listed as an EKA, I send the match a pleasant note. I’m not sure they make the connection between what they entered and what is being displayed to their matches. If they have included or linked to a tree, I tell them who, in their tree, is their mtDNA EKA.

I’ve written about how to correctly add an Earliest Known Ancestor. I’ll update that article and publish again so that you can forward those instructions to people with no EKA, or male EKAs.

  • I love learning about my ancient connections. I have a new match due to the updates, who is from a neighboring area to my great-great-great-grandmother.

I love, love, LOVE Ancient Connections. They tell me who my ancestors were before I have any prayer of identifying them individually. Then I can read up on the culture from which they sprang.

I’ve also had two situations where Ancient Connections have been exceptionally useful.

One is an exact haplogroup match to my ancestor, and the burial was in a necropolis along the Roman road about 3-4 km outside the medieval “city” where my ancestor lived.

In a second case, there were two villages in different parts of the same country, hundreds of miles apart, and one burial from about 200 years before my ancestor lived was found about 10 km from one of those villages. While this isn’t conclusive, it’s certainly evidence.

  • What does the dashed line on the Time Tree mean?

Dashed lines on the time tree can mean two things.

The red dashed line, red arrow above, is the haplogroup formation date range and correlates to the dates at the top of Time Tree, not show in this screen shot. You can also read about those dates and how they are calculated on the Scientific Details tab in Discover.

The brown dashed lines, green arrow above, connect an ancient sample to its haplogroup, but the sample date is earlier than the estimated haplogroup.

At first this doesn’t make sense, until you realize that ancient samples are sometimes carbon dated, sometimes dated by proximity to something else, and sometimes dated based on the dates of the cemetery or cultural dig location.

Archaeological samples can also be contaminated, or have poor or low coverage. In other words, at this point in time, the samples are listed, but would need to be individually reviewed before shifting the haplogroup formation date. Haplogroup formation dates are based on present day testers.

  • A cousin and I have been mtDNA tested. What might be gained by testing our other six female cousins/10 or so male cousins?

Probably not much, so here’s how I would approach this.

I would test one cousin who descends from another daughter of the EKA, if possible. This helps to sift out if a haplogroup-defining mutation has occurred.

If you or that cousin has private variants left over after their haplotype cluster is formed,  testing a second person from that line may well results in a new haplogroup formation for that branch.

I absolutely would ask every single one of those cousins to take an autosomal test, however, because you never know what tools the future will bring, and we want to leverage every single segment of DNA that our ancestors carried. Testing cousins in the only way to find those.

  • In the Mitotree, I am grouped in a haplogroup that, according to the Mitotree Match Time Tree, branched off only about 200 years ago and has four mtDNA testers in it, including me. In fact, my earliest known maternal line ancestor I found using pen-and-paper genealogy was indeed born around 230 years ago and is also the known maternal ancestor for one of these three testers – confirming the Mitotree grouping is correct. But the other two matches in this haplogroup are completely unknown to me. Unfortunately, they do not have a tree online, and they did not respond to several messages. Is there any way to find out more about them using the new Mitotree tools?

First of all, this is great news. Having said that, I share your frustration. However, you’re a genealogist. Think of yourself as a sleuth.

I’d start by emailing them, but in this case, you already have. Tell them what you know from your line and ask if their line is from the same area? End with a question for them to answer. Share tidbits from Discover – like Ancient Connections maybe. Something to peak their interest.

Next, put on your sleiuh hat. I’d google their name and email address, and check Facebook and other social media sites. I’d check to see if they match me, or any cousins who have tested, on an autosomal test. If they do match autosomally, use shared matching and the matrix tool. If they are an autosomal match, I’d also check other testing sites to see if they have a tree there.

  • One webinar attendee is haplogroup H1bb7a+151 and is frustrated because they only have eight matches and don’t understand how to leverage this.

Of course, without knowing more, I can’t speak to what they have and have not done, and I certainly understand their frustration. However, in mitochondrial and Y-DNA, you really don’t want thousands of matches. It’s not autosomal. You want close, good matches, and that’s what the Mitotree plus haplotype clusters provide.

Your personal goals also make a lot of difference.

For me, I wanted to verify what I think I know – and received a surprise. I also want to go further back if possible. Then, I want to know the culture my ancestors came from.

First, step through every single one of Discover’s 13 tools and READ EVERY PAGE – not skim. These are chapters in your free book about your ancestor.

Their haplogroup was formed about 1200, so all of those matches will be since that time. The Ancient Connections tell me it’s probably British, maybe Irish – but they will see more from their account than I can see on the public version of Discover.

The Time Tree shows me one haplotype cluster, which is where the tester’s closest matches will probably be, barring a mutation or heteroplasmy.

Looking at the matches, e-mail people, look for common locations in their trees, and see if any of them are also autosomal matches using the Advanced Matching tool.

Looking at the 10 success story examples I used, one man was able to connect 19 of his matches into three groups by doing their genealogy for them. This doesn’t work for everyone, but it will never work if we don’t make the attempt.

  • An attendee would like to search on the Earliest Known Ancestor’s (EKA’s) name field.

I would like that too. You can search on surnames, but that’s often not terribly useful for mitochondrial DNA. The Match Time Tree shows the EKA for all full sequence testers.

In the upper right hand corner of your Matches page, there’s an “Export CSV” file link. Click there to download in a spreadsheet format. The EKA is a column in that file, along with both the new Mitotree haplogroup and haplotype F number, and it’s very easy to do a sort or text search from there.

  • Several questions about why people have so many more autosomal matches than either Y-DNA or mitochondrial.

There are several considerations.

First, autosomal testing became very popular, often based on ethnicity. There are many times more autosomal testers than there are either Y or mitochondrial.

Second, if you look back just six generations, you have 64 lineages. Y-DNA and mtDNA tests one line each and you don’t have to figure out which line. It also reaches back much further in time because it’s not admixed, so nothing washes out or rolls off in each generation like with autosomal.

Third, the Y-DNA and mitochondrial DNA tests are very specific and granular.

More is not necessarily better. You’re looking for refinement – and mitochondrial is just one line. No confusion. Think how happy you’d be if your autosomal matches weren’t all jumbled together and could be placed into 64 neat little baskets. Think how much time we spend sorting them out by shared matches and other criteria. Both Y-DNA and mitochondrial is already sorted out.

I’ve broken through several brick walls with unrecombined Y-DNA and mitochondrial DNA that could never be touched with autosomal – especially older lines where autosomal DNA is either gone or negligible.

  • You mentioned a Facebook group where I can ask questions about mitochondrial DNA?

The mitochondrial DNA Facebook group is the FamilyTreeDNA mtDNA Group, here.

  • To the webinar attendee who came to see me more than 20 years ago at Farmington Hills, Michigan, at one of my first, if not the first, genetic genealogy presentation – thank you!

Thank you for attending then when I really had no idea if ANYONE would come to hear about this new DNA “thing” for genealogy. I remember how nervous I was. And thank you for sticking around, continuing to research, and saying hello now!

Closing Comment

Mitochondrial DNA testing is different than autosomal, of course. It’s often the key to those females’ lines with seemingly insurmountable brick walls.

I attempt to collect the mitochondrial DNA of every ancestor. I trace “up the tree” to find people to test who descend from those ancestors through all women to the current generation, which can be males.

To find testers, I shop:

  • Autosomal matches at FamilyTreeDNA
  • Projects at FamilyTreeDNA
  • WikiTree
  • FamilySearch
  • Ancestry DNA matches
  • Ancestry Thrulines
  • Ancestry trees
  • MyHeritage DNA matches, where ther are a lot more European testers
  • MyHeritage Theories of Family Relativity
  • MyHeritage Cousin Finder
  • Relatives at RootsTech during the month before and after RootsTech when it’s available
  • Facebook Genealogy and family groups that appear relevant

When I find an appropriately descended person, I ask if they have already taken either the Y-DNA or mitochondrial DNA test, whichever one I’m searching for at that moment. If yes, hurray and I ask if they will share at least their haplogroup. If they haven’t tested, I tell them I’m offering a testing scholarship.

I will gladly explain the results if they will share them with me. Collaboration is key and a rising tide lifts all ships.

My mantra in all of this is, “You don’t know what you don’t know, and if you don’t test, you’ll never know.” I’ve missed testing opportunities that I desperately wish I hadn’t, so test your DNA and find testers to represent your ancestors.

I hope you enjoyed the webinar. It’s not too late to watch.

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Mitotree Webinar – What It Is, How We Did It, and What Mitotree Means to You

You’re invited to a free free webinar at Legacy Family Tree Webinars titled Rewriting the Tree of Humankind: The Million Mito Project – What Is It, How We Did It, and What It Means To You.

Think of this as a peek inside the Million Mito Project – an insider view of the process of creating the new Mitotree. As both a genealogist and scientist, being a member of the dream team that birthed the new Mitotree has been the opportunity of a lifetime. We’re not finished yet, either! The Mitotree lives, and new releases and features provide new discoveries every day.

For example, our next release will add another 5,000 branches, bringing the total from 40,000 to about 45,000.

You can sign up, here, and join me live this Friday, June 6th, at 2 PM EDT. The webinar remains free for the following 7 days. After that, it will be added to the subscription library of over 2400 webinars, and members can watch at any time, plus download the included handouts.

This webinar is similar to a TED talk and covers what has changed with the release of the new Mitotree, and why. The tree has its own genealogy and “history” and it’s a fascinating story about what we did and why – challenges we never expected, and how we overcame them in new ways to make mitochondrial DNA even more valuable to genealogists.

You don’t need to understand the science behind mitochondrial DNA to enjoy this webinar. So, make yourself a nice cuppa something and enjoy learning about how we developed new scientific methodologies to create better ways to break through those maternal line brick walls. The results are incredible!

What’s This All About?

The mitochondrial tree of humanity has been rewritten, connecting all of us more succinctly than ever before on the new Mitotree.

Everyone receives mitochondrial DNA from their mother with no admixture from the father, unlike autosomal DNA. This unique feature makes mitochondrial DNA very unique and extremely useful for genealogy. Your mother received her mitochondrial DNA from her mother, then mother to daughter, all the way back in time to Mitochondrial Eve.

Mitochondrial DNA is never admixed with the DNA of the other parent, so you never have to sort out which lines it comes from. We are all leaves on the twigs on the branches of the tree of humankind and mitochondrial DNA shows you exactly where you fit, how you got there, and who else is there with you.

I don’t know about you, but I want to know where my ancestors came from – even if I don’t know their names beyond my end-of-line brick wall. I can still learn about who they were and now, with new matching tools, you can focus on which matches may solve those brick-wall mysteries.

The mitochondrial tree had not been updated since 2016, but now, with more than a million samples to work with, 50 times more than before, the tree structure has been expanded eight-fold (soon to be nine) by combining samples from academic publications, ancient DNA, public sources, and testers at FamilyTreeDNA.

The new Mitotree and companion tools provide information never before available to genealogists about their matrilineal lineages. In addition to the vastly expanded genetic tree, FamilyTreeDNA rolled out mtDNA Discover that provides a dozen fascinating chapters in your mitochondrial book.

As a Million Mito Team member, I’ll explain the challenges we overcame to create the tree of humanity – and how the new Mitotree is useful to genealogists. All genealogists can benefit, because everyone has mitochondrial DNA that holds the key to information never before available!

Let those brick walls fall!!!

Sign up to reserve your space and see you on Friday!!

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If you haven’t already subscribed (it’s free,) you can receive an e-mail whenever I publish by clicking the “follow” button on the main blog page, here.

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The Mystery of the Blue Fugates and Smiths: A Study in Blue Genes and Pedigree Collapse

The story of the Blue Fugates, an Appalachian family, is quite interesting, from a genetic perspective, a genealogical perspective, and a genetic genealogy perspective.

Who Are the Blue Fugates?

Martin Fugate, supposedly an orphan from France, and his bride, Elizabeth Smith, who had married by 1840, have long been attributed as the progenitors of the Blue Fugate Family of Troublesome Creek, in and around Perry County, Kentucky.

Their descendants were known as “The Blue Fugates” and also “The Blue People of Kentucky” because some of their children and descendants carried a recessive autosomal genetic trait, Methemoglobinemia.

Methemoglobinemia causes the skin to appear blue due to an oxygen deficiency in the red blood cells. Some people only exhibit this characteristic, or even just blue tinges in their fingernails and lips, when they are cold or agitated, such as when infants cry. Yet others are very, very blue.

Inheritance

In order for someone to exhibit the autosomal recessive trait of blueness due to Methemoglobinemia, they must inherit a copy of the gene from BOTH PARENTS. That’s why this trait is so rare.

  • If the parents have only one copy each, they are carriers and will not have the condition themselves.
  • If one parent carries either one or two copies, and the other parent does NOT carry a copy, their offspring CANNOT carry two copies of the mutation and will not be blue.
  • If both parents carry a copy, and both parents pass their copy on to their offspring, the offspring will probably exhibit some level of blueness – from just a tinge when they are cold, ill or or upset, to very, very blue.

I’m not a physician, so I’m not delving into the medical specifics of Methemoglobinemia, but suffice it to say that levels of 10-20% of methemoglobin in the blood produce blue skin, higher levels can produce more severe medical conditions, and levels beneath that may not be visually detectible.

What’s important for the genealogy aspect of this story is that both parents must carry a copy AND pass their copy on for the condition to express in their offspring.

We’ve learned a lot since the 1800s when this was first observed in various members of the Fugate family in Perry County, KY, and since the 1960s when this phenomenon was first studied in the Fugate family and their descendants. To be clear, there are also references to the blue Combs and blue Ritchies in and around Perry County – but the common factor is that they have ancestors that descend from the Fugate family AND the Smith family ancestors, both.

During my research, I’ve proven some of what was initially accepted as fact was incorrect – and I’d like to correct the record. Bonus points too, because it’s just such a great genealogy story!

My Interest

I’ve been inordinately interested in the Fugate family for a long time – but not because of their famous blueness.

The Fugate family has been found for more than 225 years alongside my Cook, Claxton, Campbell, and Dobkins families. First, in Russell County, VA, where Josiah Fugate was granted land along Sword’s Creek in 1801 that adjoined Harry Smith, Richard Smith, and others, including my brick-wall ancestor, Joel Cook. Keep in mind that we have never discovered the birth surname of Joel’s wife or Joel’s parents.

Joel’s daughter, Sarah, married James Claxton about 1799 or 1800 in Russell County, and in February of 1802, James Claxton and Zachariah Fugate, among others, were ordered to view and lay out a new road. They were clearly neighbors, living on the same road, and knew each other well. We don’t know who James’ parents were either.

The Fugates first lived adjacent to the Cook, Riley, Stephens, and Claxton families on Mockason Creek in Russell County, then later migrated with the same group of families to Claiborne County where they lived along the Powell River near the Lee County, VA line, and are very closely associated with the Dobkins and Campbell lines.

Sometime between 1802 and 1805, several Russell County families moved 110 miles down the mountain range and settled together on the Powell River in Claiborne County, TN.  About the same time, others from the same cluster moved to what would eventually become Perry County, KY.

In 1805, the Fugates were ordered as road hands on the north side of Wallen’s Ridge in Claiborne County, the part that would become Hancock County in the 1840s, along with James Claxton and several Smiths.

In 1808, James Claxton witnessed a deed to Henley Fugate and John Riley.

The unsubstantiated family rumor, repeated as fact but with no source, has always been that William Fugate married the sister of my John Campbell. If that were true, tracking the Fugates would help me track my Campbells – yet another brick wall. Hence, my early interest in the Fugate family. Until now, I’ve never solved any part of that puzzle.

In 1827, in Claiborne County, Henry Cook, road overseer, is assigned John Riley, Henly Fugate, William Fugate, Fairwick Claxton (son of James who had died in 1815), and others. These families continued to be allied, living close to each other.

In 1842, William Fugate (1799-1855), born to William Fugate and Sarah Jane Stephens in Russell County, is involved in the estate of John Campbell, born about 1772, who had died in 1838. John Campbell was the husband of Jane “Jenny” Dobkins, daughter of Jacob Dobkins (1751-1835).

William Fugate of Claiborne County signed a deposition in 1851 saying he came to Claiborne County, TN, in 1826. Claiborne County is rugged terrain, located on the south side of the Cumberland Gap, where Virginia, Tennessee, and Kentucky intersect.

In 1853, both William Fugate and Jehiel Fugate are neck-deep in lawsuits surrounding the estate of Jacob Dobkins, who died in 1835, lived on Powell River, and whose daughters married John Campbell and his brother George Campbell

I recently discovered that this William Fugate was born about 1799 in Russell County, VA, and according to his son’s death certificate, William’s wife was Nancy Riley, which makes a lot of sense, given the proximity of these families. I must admit, I’m glad to solve this, but I’m also disappointed that he wasn’t married to John Campbell’s sister.

So, why does any of this matter in the Blue Fugate story?

In part, because I knew decades ago that Martin Fugate, of the Kentucky Blue Fugates, was not an orphan from France who had somehow made his way to the eastern shores of Maryland, then to Perry County, KY by 1820 when he supposedly received a land grant. That land grant date doesn’t square with Martin’s birth year of 1820 either, nor his marriage about 1840, both of which are substantiated by the census.

You can see from the information gleaned from Russell County that the Fugate family was there well before 1800. In fact, a Martin Fugate is shown on the 1789 tax list and other Fugates were there earlier, as early as 1771, according to extracted Russell County records in the book “The Fugate Family of Russell County, Virginia” by David Faris. The Fugate descendants continued to press on westward from there. Fugate, unlike Smith, Cook, and even Campbell, is not a common surname.

“Orphan” stories are often early ways that people said “I don’t know”, without saying, “I don’t know where he came from”, so they speculated and said “maybe he was an orphan.” Then that speculation was eventually passed on as fact.

That might have been happening in Perry County in the 1960s, but in Claiborne County in the 1980s, family members were telling me, “Martin waren’t no orphan,” and would roll their eyes and sigh with great exasperation. You could tell this was far from the first time they had had to combat that story. To be clear, the Fugate family lived down along Little Sycamore Creek with my Estes, Campbell and other ancestral families. In the 1980s, I was finding the oldest people possible and talking to them.

Some records in Russell County, where the Fugates of Perry County, KY, and the Fugates of Claiborne County, TN, originated, did and do exist, so could have been researched in the 1960s, but you would have had to know where to look. No one back then knew that the Perry County Fugates originated in Russell County, so they wouldn’t have known to look there. Research wasn’t easy. If they had known to look in Russell County, they would have had to travel there in person to review records. Early records exist in Perry County, too, but in the 1960s, not even the census was available, and people simply didn’t remember back to the early to mid-1800s.

Truthfully, no one would ever have doubted those early stories that had been handed down. They were revered, in all families, and treated as gospel. Those stories were the only connection they had to their ancestors – and the generations inbetween who passed them on. Nope, no one was going to question what Grandpa or Uncle Joe said.

So, in the 1960s, when the Blue Fugates in Perry and adjacent Breathitt County, KY were first studied by Dr. Cawein and his nurse, Ruth Pendergrass, they gathered oral family history and constructed a family pedigree from that information. They documented who was blue from first-hand eye-witness accounts – which would only have stretched back into the late 1800s, best case.

It probably never occurred to anyone to validate or verify earlier information that was provided. Plus, it would have been considered rude. After all, they weren’t genealogists, and they were trying to solve a medical mystery. The information they collected did not conflict with what was known about the disease and how it was transmitted, so they had no reason to doubt its historical accuracy.

The Mystery of the Blue Fugates?

The Blue Fugates were a family renowned for their blue skin – at least some of them had blue skin. That’s part of what makes this story so interesting.

Originally, it was believed that only one progenitor couple was involved, Martin Fugate and his wife, Elizabeth Smith, but now we know there were two. Maybe I should say “at least two.”

Martin Fugate and his bride, Elizabeth Smith, whose first known child was born in 1841, according to the 1850 census, are progenitors of the Blue Fugate Family of Troublesome Creek, but they aren’t the only progenitors.

Martin was not shown in the Perry County, KY 1840 census, but two Zachariah Fugates are present, 8 Fugate families are found in neighboring Breathitt County, more than a dozen in Russell County and surrounding counties in Virginia, and four, including two William Fugates, in Claiborne County, TN. The younger of the two lived next door to John Dobkins, son of deceased Jacob Dobkins.

Martin Fugate (c1820-1899) of Perry County and his second cousin, Zachariah Fugate (1816-1864), who each married a Smith sister, are both progenitors of the Blue Fugates through their common ancestor, their great-grandfather, Martin Fugate, who was born in 1725 and died in 1803 in Russell County, VA.

Obviously, if Martin (c1820-1899) had a Fugate second cousin who also lived in Perry County, Martin wasn’t an orphan. That knowledge is due to more recently available information, like census and other data – and that’s part of what I want to correct.

In 1948, Luke Combs, from Perry County, KY, took his sick wife to the hospital, but Luke’s blueness caused the medical staff to focus on him instead, thinking he was experiencing a medical emergency. He wasn’t. His skin was just blue. In 1974, Dr Charles H. Behlen II said, ‘Luke was just as blue as Lake Louise on a cool summer day.’ The Blue Fugates were “discovered” by the rest of the world, thanks to Luke, but they were nothing new to local people, many of whom did not welcome the notoriety.

In the 1960s, hematologist Madison Cawein III, with the assistance of Ruth Pendergrass, studied 189 members of the extended Fugate family, treated their symptoms, and published his findings. He included a pedigree chart, but not everyone was keen on cooperating with Dr. Cawein’s research project.

The Fugate family history collected for the study was based on two things:

  • Personal knowledge of who respondents knew was blue
  • Remembered oral history beyond the reach of personal knowledge.

That remembered oral history reported that Martin Fugate and Elizabeth Smith’s youngest son, Zachariah Fugate (born in 1871), married his mother’s (older) sister, Mary Smith, (born about 1820), and had a family. I’ve added the dates and information in parentheses, or they would have immediately known that marriage was impossible. Or, more directly, even if they married when Zachariah was 14, Mary would have been 70 years old, and they were certainly not going to produce offspring. This is the second piece of information I want to correct. That marriage never happened, although people were accurate that:

  • Martin Fugate and his wife, Elizabeth Smith, did have a son named Zachariah Fugate
  • One Zachariah Fugate did marry Mary Smith, sister of Elizabeth Smith

It’s just that they were two different Zachariah Fugates, born 75 years apart. Same name confusion strikes again.

I constructed this census table of Martin Fugate with Elizabeth Smith, and Zachariah Fugate with Mary Smith. They lived next door to each other in Perry County – and it seemed that every family reused the same “honoring” names for their children – and had been doing such for generations.

In the 1960s, when the information was being compiled for Dr. Cawein, the census and other documents that genealogists rely on today were not readily available.

Furthermore, genetically, for the mystery Dr. Cawein was attempting to solve, it didn’t really matter, because it was still a Smith female marrying a Fugate male. I know that it made no difference today, but he wouldn’t have known that then. To track down the source of the blueness, he needed to identify who was blue and as much about their ancestors as possible.

The Zachariah Fugate (1816-1864) who married Elizabeth Smith’s sister, Mary Smith, was Martin Fugate’s second cousin by the same name, Zachariah. Both Martin (c1820-1899) and his second cousin, Zachariah (c1816-1864), married to Smith sisters, had blue children, which helps cement the fact that the responsible genes were passed down through BOTH the Fugate and Smith lines, and weren’t just random mutations or caused by environmental or other factors.

Proof

In case you’re wondering exactly how I confirmed that Martin and Zachariah did indeed marry Elizabeth and Mary Smith – their children’s birth and death records confirmed it. These records correlate with the census.

Unlike most states, Kentucky has some pre-1900 birth and death records.

Wilson Fugate’s birth in February, 1855 was recorded, naming both of his parents, Martin Fugate and Elizabeth Smith.

Martin Fugate and Elizabeth Smith’s son, Henley or Hendley, died in 1920, and his death certificate gave the names of both parents. Betty is a nickname for Elizabeth.

On the same page with Wilson Fugate’s birth, we find a birth for Zachariah Fugate and Mary Smith, too.

Hannah Fugate was born in December 1855.

Zachariah Fugate and Mary Smith’s son, Zachariah died in 1921, and his death certificate gives his parents as Zach Fugate and Polly Smith, a nickname for Mary.

There are more death records for children of both sets of parents.

Both couples, Martin Fugate and Elizabeth Smith, and Zachariah Fugate and Mary Smith, are progenitors of the Blue Fugate family.

Of Martin’s 10 known children, 4 were noticeably “blue” and lived long, healthy lives. At least two of Zachariah’s children were blue as well.

Some people reported that Martin, himself, had deep blue skin. If so, then both of his parents would have carried that genetic mutation and passed it to him.

Unfortunately, color photography didn’t exist when Martin (c1820-1899), lived, so we don’t know for sure. For Martin’s children to exhibit blue skin, they would have had to inherit a copy of the gene from both parents, so we know that Martin’s wife, Elizabeth, also inherited the mutation from one of her parents. Ditto for Zachariah Fugate and Mary Smith. The chances of two families who both carry such a rare mutation meeting AND having two of their family members marry are infinitesimally small.

Dr. Cawein’s Paper

In 1964, Dr. Cawein published his findings, but only with a pedigree chart with no names. What was included was an explanation about how remote and deep the hills and hollows were, and that out-migration was almost impossible, explaining the propensity to marry cousins.

Legend:

  • Measured – Found to have elevated methemoglobin
  • Measured – Found to have decreased methemoglobin
  • Not measured – Reported to be “blue”
  • Measured – Found to be normal

Cawein further stated that data was collected by interviewing family members who personally knew the individual in question and could say if they were actually blue.

Cawein erroneously reported that “Martin Fugate was an orphan born about 1800, landed in Maryland, obtained a land grant in Perry County, KY in 1820, and married a local gal. From 1820 to about 1930, the population consisted of small, isolated groups living in creek valleys and intermarriage was quite common.” Bless his heart.

Later, geneticist Ricky Lewis wrote about the Blue Fugates, sharing, among other things, the provenance of that “blue” family photo that circulates on the internet, revealing that it is a composite that was assembled and colorized back in 1982. She also erroneously stated that, “after extensive inbreeding in the isolated community—their son married his aunt, for example—a large pedigree of “blue people” of both sexes arose.” Bless her heart too.

Dr. Lewis is incorrect that their son married his aunt – but she’s right that intermarriage between the families is responsible for the blue descendants. In colonial America, and elsewhere, cousin marriages were fairly common – everyplace. You married who you saw and knew. You saw your family and neighbors, who were generally your extended family. No left-handed apology needed.

Pedigree collapse, sharing the same ancestors in multiple places in your tree, is quite common in genealogy, as is endogamy among isolated populations.

Today, things have changed somewhat. People move into and out of an area. The younger generation moves away a lot more and has for the past 100+ years. Most people know their first cousins, but you could easily meet a second or third cousin and never know you were related.

While early stories reported that Martin Fugate (c1820-1899) was an orphan from France, mysteriously appearing in Kentucky around 1820, later genealogical evidence as well as genetic research proves that Martin Fugate was actually born about 1820, in Russell County, VA and his ancestors, over several generations, had followed the typical migration path across Virginia into Kentucky.

We’ve also proven that Martin’s son, Zachariah (born 1871) was not the Zachariah who married Elizabeth Smith’s sister, Mary, who was 50 years old when Zachariah was born.

What else do we know about these families?

The Back Story

Compared to the Smith story, the Fugate story was “easy.”

Don’t laugh, but I spent several days compiling information and charting this in a way I could see and understand in one view.

I hesitate to share this, but I’m going to because it’s how I think. I also put together a very basic Fugate tree at Ancestry, here. Many children and siblings are missing. I was just trying to get this straight in my mind.

Click to enlarge any image

This spreadsheet is color-coded:

  • The text of each lineage has a specific color. For example, Fugates are blue.
  • Some people (or couples) are found in multiple descendants’ lines and are duplicated in the tree. Duplicated people also have a cell background color. For example, Mahala Richey (Ritchey, Ritchie) is highlighted yellow. James and Alexander Richey have green text and apricot background because they are duplicated.
  • The generation of parents who had blue children is marked with black boxes and the label “Blue Kids.”
  • Only the blue kids for this discussion are listed below those couples.
  • The bluest person was Luna Fugate (1886-1964).
  • While Luna’s husband, John Stacey, also descended from the Smith/Combs line, only one of their children expressed the blue trait. That child’s lips turned blue when they cried. John and Luna were actually related in three ways. Yes, my head hurts.
  • The last known “blue” person was Luna Fugate’s great-grandchild, whose name I’ve obfuscated.

Ok, let’s start with the blue Fugates on our spreadsheet. You’ll probably want to follow along on the chart.

Martin Fugate (1725-1803) and wife Sarah, had several children, but only two, the ones whose grandchildren married Smith sisters are known to have had blue children.

On our chart, you can see that Martin (1725-1803) is blue, and so is Son 1, William Fugate and Sarah Stephens, along with Son 2, Benjamin Fugate and Hannah Devers. Both William and Benjamin are mentioned in Martin’s estate in 1803 in Russell County, VA.

Two generations later, Martin Fugate (c1820-1899) and Elizabeth Smith had four blue children, and Zachariah Fugate (c1816-1864) and Mary Smith had at least two blue children. Furthermore, Zachariah Fugate’s sister, Hannah (1811-1877), married James Monroe Richie.

The Richey’s are green, and you can see them on both the left and right of the chart. Hannah’s husband descended from the same Richey line that Elizabeth Smith did. It was no surprise when their child, Mahala Ritchie (1854-1922), married Levi Fugate, to whom she was related three ways, they became the parents of a blue child. Their daughter, Luna Fugate, was known as “the Bluest of the Blue Fugates.”

Mahala Ritchie (1854-1922) could have inherited her blue gene (or genes) from either her mother Hannah Fugate, or her father, James Monroe Ritchie, or both. We don’t know if Hannah was blue or not.

We do know that Mahala married Levi Fugate, her third cousin through the Fugate line, and her third and fourth cousin also through the Richie and Grigsby lines, respectively. This is the perfect example of pedigree collapse.

You can see the purple Grigsby lines in the center and to the right of the pedigree chart too, with Benjamin Grigsby, highlighted in blue, being common to both lineages.

Zachariah Fugate (1816-1864) and Mary Smith had at least two blue sons, but I am not tracking them further. Suffice it to say that Blue John married Letha Smith, his first cousin, the granddaughter of Richard Smith and Nancy Elitia Combs. Lorenzo, “Blue Anze”, married a Fugate cousin, so it’s no surprise that Zachariah and Mary were also progenitor couples of the Blue Fugates.

Martin’s son, Levi Fugate, married Mahala Ritchie, mentioned above, and had Luna Fugate who would have been personally known to Dr. Cawein. Luna, pictured above, at left, was known as the bluest of the Blue Fugates.

Luna married John Stacey who some thought wasn’t related to Luna, so it was confusing why they had one child that was slightly blue. However, John turns out to be Luna’s second cousin, third cousin once removed and first cousin once removed through three different lines. His great-grandparents were Richard Smith and Nancy Combes. Since one of their children had a slight blue tinge, John, while not visibly blue himself, clearly carried the blue gene.

Where Did the Blue Gene Come From?

The parents of Elizabeth Smith and Mary Smith were Richard Smith and Nancy (Eletia) Combs. His Smith ancestors include both the Richeys and Caldwells.

James Richey (1724-1888) married Margaret Caldwell (1729-1802) and his father, Alexander Richey (1690-1749) married Jeanne Caldwell (1689-1785). While the Caldwell females weren’t closely related, Jeanne was the daughter of Joseph Alexander Caldwell (1657-1730) and Jane McGhie, and Margaret Caldwell (1729-1802) was the great-granddaughter of that couple. The Caldwells are shown in magenta, with both Richey/Caldwell couples shown as duplicates. The Richey are highlighted in apricot, and the Caldwell’s with a light grey background. It was difficult to show how these lines connect, so that’s at the very top of the pedigree chart.

When just viewing the Smith-Combs line, it’s easier to view in the Ancestry pedigree.

The Smith, Richey, Combs, Grigsby, and Caldwell lines are all repeated in different locations in the trees, such as with Hannah Fugate’s husband. These repeated ancestors make it almost impossible for us to determine where in the Smith ancestral tree that blue gene originated.

We don’t know which of these ancestral lines actually contributed the blue gene.

Can We Figure Out Where the Blue Gene Came From?

How could we potentially unravel this mystery?

We know for sure that the blue gene in the Fugate side actually descends from Martin Fugate who was born in 1725, or his wife, Sarah, whose surname is unknown, because their two great-grandchildren, Martin (c1820-1899) and Zachariah (1816-1864) who both married Smith sisters had blue children. For those two intervening generations between Martin Fugate (1725-1803) and those two great-grandsons, that blue gene was quietly being passed along, just waiting for a blue Fugate gene carrier to meet another blue gene carrier. They found them in the Smith sisters.

None of Martin (1725-1803) and Sarah’s other children were known to have had any blue children or descendants. So either they didn’t carry the blue gene, or they didn’t marry someone else who did – that we know of.

We can’t tell on the Smith side if the blue gene descends from the Smith, Richey, Grigsby or Caldwell ancestors, or maybe even an unknown ancestor.

How can we narrow this down?

If a Fugate in another geographic location married someone from one of these lineages, say Grigsby, for example, and they had blue offspring, and neither of them shared any of the other lineages, then we could narrow the blue gene in the Smith line to the Grigsby ancestor.

Unfortunately, in Perry and surrounding counties in Kentucky, that would be almost impossible due to intermarriage and pedigree collapse. Even if you “think you know” that there’s no connection through a third line, given the deep history and close proximity of the families, the possibility of unknown ancestry or an unexpected parent is always a possibility.

Discover

While the blue gene is not connected to either Y-DNA or mitochondrial DNA, we do have the Fugate’s Y-DNA haplogroup and the Smith sisters’ mitochondrial DNA.

Y-DNA

The Big Y-700 haplogroup for the Martin Fugate (c1820-1899) line is R-FTA50432, which you can see, here..

You can see the Blue Fugate Family by clicking on Notable Connections.

If you’re a male Fugate descendant who descends from anyone other than Martin Fugate (c1820-c1899), and you take a Big Y test, you may well discover a new haplogroup upstream of Martin (c1820-1899) that represents your common Fugate ancestor.

If you descend from Martin, you may find youself in either of the two haplogroups shown for Martin’s descendants, or you could split the line to form a new haplogroup.

We don’t have the mitochondrial DNA of Martin Fugate (c1820-1899), which would be the mitochondrial DNA of his mother, Nancy Noble. We also don’t have the the mtDNA of Mary (Polly) Wells, the mother of Zachariah Fugate (c1816-1864). If you descend from either of these women in a direct matrilineal line, through all women, please take a mitochondrial DNA test and reach out. FamilyTreeDNA will add it as a Notable Connection.

We do, however, have the mitochondrial DNA of Elizabeth and Mary Smith

Mitochondrial DNA of Elizabeth and Mary Smith

The mitochondrial DNA of both Elizabeth and Mary Smith follows their mother’s line – Nancy Combs through Nancy (Eletia?) Grigsby. Nancy’s mother is unknown, other than the possible first name of Margaret.

Nancy Grigsby’s descendant is haplogroup K1a61a1, which you can see here.

The Blue Fugates show under Notable Connections.

The Smith sisters’ haplogroup, K1a61a1, tells us immediately that their ancestor is European, eliminating other possibilities.

The time tree on Discover is quite interesting

Haplogroup K1a61a1 was formed about the year 1400. Descendants of this haplogroup are found in the UK, Scotland, England, several unknown locations, and one person who selected Native American, which is clearly in error. Haplogroup K is not Native American.

By focusing on the haplotype clusters, identified by the F numbers in the elongated ovals, our tester may be able to identify the mother of Nancy Grigsby, or upstream lineages that they can work back downstream to find someone who married Thomas Grigsby.

This story is far from over. In fact, a new chapter may just be beginning.

If you’re a Fugate, or a Fugate descendant, there’s still lots to learn, even if autosomal DNA is “challenging,” to say the least, thanks to pedigree collapse. Testing known females lineages can help us sort which lines are which, and reveal their hidden stories.

Other resources if you want to read more about the Fugates: The Blue People of Troublesome Creek, Fugates of Kentucky: Skin Bluer than Lake Louise, Those Old Kentucky Blues: An Interrupted Case Study, and Finding the Famous Paintings of the Blue People of Kentucky.

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Discover’s Ancient Connections – How Are You Related?

When FamilyTreeDNA released the new Mitotree, they also introduced their new mtDNA Discover tool, which is a series of 13 reports about each haplogroup, including one titled Ancient Connections.

Ancient Connections shows you ancient relatives from your direct matrilineal line through a mitochondrial DNA test or through a Y-DNA (preferably Big Y-700) test.

Ancient Connections help you connect the present to the past based on archaeological excavations around the world and DNA sequencing of remains. Ancient Connections links you through your DNA to ancient people, cultures, and civilizations that would be impossible to discover any other way. You don’t have to wonder if it’s accurate, or which line it came from, because you know based on the test you took. Discover’s Ancient Connections track the journey of your ancestors and relatives.

Ancient Connections can be very exciting – and it’s easy to get swept away on a wave of jubilation.

Are those people your ancestors, or relatives, or what? How do you know? How can you figure it out?

So let me just answer that question generally before we step through the examples, so you can unveil your own connections.

  • You are RELATED to both Ancient and Notable Connections. Notable Connections are famous or infamous people who have lived more recently, and their relatives have been tested to identify their haplogroups.
  • It’s VERY unlikely that Ancient Connections are your direct ancestors – but someone in the line that you share IS your ancestor.
  • Many factors enter into the equation of how you are related, such as the haplogroup(s), the timeframe, and the location.
  • The sheer number of people who were living at any specific time makes it very unlikely that any one person with that haplogroup actually was your direct ancestor. They are much more likely to be your distant cousin.

Factors such as whether you share the same haplogroup, similar locations, and the timeframe make a huge difference. Everyone’s situation is different with each Ancient Connection.

Ok, are you ready for some fun???

Let’s find out how to leverage these tools.

Ancient Connections

Ancient connections are fun and can also be quite useful for genealogy.

In this article, I’m going to use a mitochondrial DNA example because full sequence testers at FamilyTreeDNA just received their new Mitotree haplogroup. mtDNA Discover was released with Mitotree, so it’s new too. However, the evaluation process is exactly the same for Y-DNA.

Everyone’s results are unique, so your mileage absolutely WILL vary. What we are going to learn here is a step-by-step analytical process to make sure you’re hearing the message from your ancestors – and interpreting it correctly.

To learn about your new mitochondrial DNA haplogroup and haplotype, read the articles:

Radegonde Lambert

Let’s start with an Acadian woman by the name of Radegonde Lambert. She’s my ancestor, and I wrote about her years ago in the article, Radegonde Lambert (1621/1629-1686/1693), European, Not Native.

At the time, that article caused a bit of a kerfluffle, along with the article, Haplogroup X2b4 is European, Not Native American, because Radegonde’s X2b4 haplogroup had been interpreted by some to mean that her matrilineal ancestors were Native American.

That often happens when a genealogical line abruptly ends and hits a brick wall. What probably began with “I wonder if…”, eventually morphed into “she was Native,” when, in fact, she was not. In Radegonde’s case, it didn’t help any that her haplogroup was X2b4, and some branches of base haplogroup X2 are in fact Native, specifically X2a, However, all branches of X2 are NOT Native, and X2b, which includes X2b4, is not.

The Acadians were French people who established a colony in what is now Nova Scotia in the 1600s. They did sometimes intermarry with the Native people, so either Native or European heritage is always a possibility, and that is exactly why DNA testing is critically important. Let’s just say we’ve had more than one surprise.

I always reevaluate my own work when new data becomes available, so let’s look to see what’s happening with Radegonde Lambert now, with her new haplogroup and mtDNA Discover.

Sign on and Identify Your Haplogroup

You can follow along here, or sign on to your account at FamilyTreeDNA.

The first step is to take note of your new Mitotree haplogroup.

Your haplogroup badge is located near the bottom right of your page after signing in.

The tester who represents Radegonde Lambert has a Legacy Haplogroup of X2b4 and has been assigned a new Mitotree haplogroup of X2b4g.

Click Through to Discover

To view your personal Discover information, click on the Discover link on your dashboard.

You can simply enter a haplogroup in the free version of mtDNA Discover, but customers receive the same categories, but significantly more information if they sign in and click through.

You can follow along on the free version of Discover for haplogroups X2b4 here, and X2b4g here.

Clicking on either the Time Tree, or the Classic Tree shows that a LOT has changed with the Mitotree update.

Each tree has its purpose. Let’s look at the Classic Tree first.

The Classic Tree

I like the Classic Tree because it’s compact, detailed and concise, all in one. Radegonde Lambert’s new haplogroup, X2b4g is a subgroup of X2b4, so let’s start there.

Click on any image to enlarge

Under haplogroup X2b4, several countries are listed, including France. There are also 7 haplotype clusters, which tell you that those testers within the cluster all match each other exactly.

It’s worth noting that the little trowels (which I thought were shovels all along) indicate ancient samples obtained from archaeological digs. In the Discover tools, you’ll find them under Ancient Connections for that haplogroup. We will review those in a minute.

In Mitotree, haplogroup X2b4 has now branched several granular and more specific sub-haplogroups.

Radegonde Lambert’s new haplogroup falls below another new haplogroup, X2b4d’g, which means that haplogroup X2b4d’g is now the parent haplogroup of both haplogroups X2b4d and X2b4g. Both fall below X2b4d’g.

Haplogroup names that include an apostrophe mean it’s an umbrella group from which the two haplogroups descend – in this case, both X2b4d and X2b4g. Apostrophe haplogroups like X2b4d’g are sometimes referred to as Inner Haplogroups.

You can read more about how to understand your haplogroup name, here.

In this case, haplogroup X2b4d’g is defined by mutation G16145A, which is found in both haplogroups X2b4d and X2b4g. Both of those haplogroup have their own defining mutations in addition to G16145A, which caused two branches to form beneath X2b4d’g.

You can see that Radegonde Lambert’s haplogroup X2b4g is defined by mutation C16301T, but right now, that really doesn’t matter for what we’re trying to accomplish.

In descending order, for Radegonde, we have haplogroups:

  • X2b4
  • X2b4d’g
  • X2b4g

Your Match Page

Looking at the tester’s match page, Radegonde’s haplotype cluster number and information about the cluster are found below the haplogroup. You can view your cluster number on:

  • Your match page
  • The Match Time Tree beside your name and those of your matches in the same haplotype cluster
  • The Scientific Details – Variants page

I wrote about haplotype clusters, here.

Click on any image to enlarge

On your match page, which is where most people look first, you are in the same haplogroup and haplotype cluster with anyone whose circle is also checked and is blue. If the little circles are not checked and blue, you don’t share either that haplogroup, haplotype cluster, or haplogroup and haplotype cluster. If you share a haplotype cluster, you will always share the same haplogroup.

Haplotype clusters are important because cluster members match on exactly the same (but less stable) mutations IN ADDITION to haplogroup-defining (more stable) mutations.

However, you may also share an identifiable ancestor with people in different haplotype clusters. Mutations, and back mutations happen – and a lot more often at some mutation locations, which is why they are considered less stable. Normally, though, your own haplotype cluster will hold your closest genealogical matches.

In Discover, you can see that Radegonde’s haplotype cluster, F585777, displays three tester-supplied countries, plus two more. Click on the little plus to expand the countries.

What you’re viewing are the Earliest Known Ancestor (EKA) countries that testers have entered for their direct matrilineal ancestor.

Let’s hope they understood the instructions, and their genealogy information was accurate.

Notice that Canada and France are both probably quite accurate for Radegonde, based on the known history of the Acadians. There were only French and Native women living in Nova Scotia in the 1600s, so Radegonde had to be one or the other.

The US may be accurate for a different tester whose earliest known ancestor (EKA) may have been found in, say, Louisiana. Perhaps that person has hit a brick wall in the US, and that’s all they know.

The US Native American flag is probably attributable to the old “Native” rumor about Radegonde, and the tester didn’t find the Canadian First Nations flag in the “Country of Origin” dropdown list. Perhaps that person has since realized that Radegonde was not Native and never thought to change their EKA designation.

The little globe with “Unknown Origins” is displayed when the tester doesn’t select anything in the “Country of Origin.”

Unfortunately, this person, who knew when Radegonde Lambert lived, did not complete any additional information, and checked the “I don’t know this information” box. Either Canada, or France would have been accurate under the circumstances. If they had tracked Radegonde back to Canada and read about her history, they knew she lived in Canada, was Acadian, and therefore French if she was not Native. Providing location information helps other testers, whose information, in turn, helps you.

Please check your EKA, and if you have learned something new, PLEASE UPDATE YOUR INFORMATION by clicking on the down arrow by your user name in the upper right hand corner, then Account Settings, then Genealogy, then Earliest Known Ancestors.

Don’t hesitate to email your matches and ask them to do the same. You may discover that you have information to share as well. Collaboration is key.

Radegonde’s Discover Haplogroup

First, let’s take a look at Radegonde’s haplogroup, X2b4g, in Discover.

The Discover Haplogroup Story landing page for haplogroup X2b4g provides a good overview. Please READ this page for your own haplogroup, including the little information boxes.

The history of Radegonde’s haplogroup, X2b4g, is her history as well. It’s not just a distant concept, but the history of a woman who is the ancestor of everyone in that haplogroup, but long before surnames. Haplogroups are the only way to lift and peer behind the veil of time to see who our ancestors were, where they lived, and the cultures they were a part of.

We can see that Radegonde’s haplogroup, X2b4g, was born in a woman who lived about 300 CE, Common (or Current) Era, meaning roughly the year 300, which is 1700 years ago, or 1300 years before Radegonde lived.

  • This means that the tester shares a common ancestor with everyone, including any X2b4g remains, between now and the year 300 when haplogroup X2b4g was born.
  • This means that everyone who shares haplogroup X2b4g has the same common female ancestor, in whom the mutation that defines haplogroup X2b4g originated. That woman, the common ancestor of everyone in haplogroup X2b4g, lived about the year 300, or 1700 years ago.
  • Your common ancestor with any one individual in this haplogroup can have lived ANYTIME between very recently (like your Mom) and the date of your haplogroup formation.
  • Many people misinterpret the haplogroup formation date to mean that’s the date of the MRCA, or most recent common ancestor, of any two people. It’s not, the haplogroup formation date is the date when everyone, all people, in the haplogroup shared ONE ancestor.
  • The MRCA, or most recent common ancestor, is your closest ancestor in this line with any one person, and the TMRCA is the “time to most recent common ancestor.” It could be your mother, or if your matrilineal first cousin tested, your MRCA is your grandmother, and the TMRCA is when your grandmother was born – not hundreds or thousands of years ago.
  • Don’t discount mitochondrial DNA testing by thinking that your common ancestor with your matches (MRCA) won’t be found before the haplogroup birth date – the year 300 in Radegonde’s case. The TMRCA for all of Radegonde’s descendants is about 1621 when she was born.
  • The haplogroup birth date, 1700 years ago, is the common ancestor for EVERYONE in the haplogroup, taken together.
  • Mitochondrial DNA is useful for BOTH recent genealogy and also reveals more distant ancestors.
  • Looking back in time helps us understand where Radegonde’s ancestors lived, which cultures they were part of, and where.

There are two ways to achieve that: Radegonde’s upstream or parent haplogroups, and Ancient Connections.

Parent Haplogroups

X2b4g split from X2b4d’g, the parent haplogroup of BOTH X2b4d and X2b4g, around 3700 years ago, or about 1700 BCE (Before Common (or Current) Era).

Looking at either the Classic Tree, the Time Tree (above) or the Match Time Tree, you can see that haplogroup X2b4g has many testers, and none provide any locations other than France, Canada, the US, unknown, and one Native in the midst of a large haplotype cluster comprised of French and Canadian locations. Due to the size of the cluster, it’s only partially displayed in the screen capture above.

You can also see that sister haplogroup X2b4d split from X2b4d’g around the year 1000, and the ancestors of those two testers are reported in Norway.

Many, but not all of the X2b4g testers are descendants of Radegonde. Even if everyone is wrong and Radegonde is not French, that doesn’t explain the other matches, nor how X2b4g’s sister haplogroup is found in Norway.

Clearly, Radegonde isn’t Native, but there’s still more evidence to consider.

Let’s dig a little deeper using Radegonde’s Ancient Connections.

Ancient Connections

While ancestor and location information are user-provided, Ancient Connections are curated from scientifically published papers. There’s no question about where those remains were found.

When signed in to your account, if you’ve taken the mtFull Sequence test, clicking on the Ancient Connections tab in Discover shows a maximum of around 30 Ancient Connections. If you’re viewing the free version of Discover, or you’ve only tested at the HVR1 or HVR1+HVR2 levels, you’ll see two of your closer and one of your most distant Ancient Connections. It’s easy to upgrade to the mtFull.

In Discover, the first group of Ancient Connections are genetically closest to you in time, and the last connections will be your most distant. Some connections may be quite rare and are noted as such.

Please keep in mind that oldest, in this case, Denisova 8 and Sima de los Huesos, will never roll off your list. However, as new studies are released and the results are added to the tree, you may well receive new, closer matches. New results are being added with each Discover update.

It’s very exciting to see your Ancient Connections, but I need to say three things, loudly.

  1. Do NOT jump to conclusions.
  2. These remains are probably NOT YOUR ANCESTORS, but definitely ARE your distant cousins.
  3. Ancient Connections ARE wonderful hints, especially when taken together with each other and additional information.

It’s VERY easy to misinterpret Ancient Connections because you’re excited. I’ve done exactly that. To keep the assumption monster from rearing its ugly head, I have to take a breath and ask myself a specific set of questions. I step through the logical analysis process that I’m sharing with you.

The first thing I always want to know is where the genetically closest set of remains was found, when, and what we know about them, so let’s start there. Keep in mind that the closest remains genetically may not be the most recent set of remains to have lived. For example, my own haplogroup will be the closest genetically, but that person may have lived 2000 years ago. An Ancient Connection in a more distant haplogroup may have lived only 1000 years ago. The closest person genetically is NOT the same as the person who lived the most recently.

Our tester, Radegonde’s descendant, has no Ancient Connections in haplogroup X2b4g or X2b4d’g, but does have two in haplogroup X2b4, so let’s start there.

Discover provides a substantial amount of information about each set of ancient remains. Click on the results you want to view, and the information appears below.

Radegonde’s first Ancient Connection is Carrowkeel 534. The graphic shows the tester, the Ancient Connection being viewed, and their shared ancestor’s haplogroup. In this case, the shared ancestor haplogroup of Carrowkeel 534 and the tester is X2b4, who lived about 5000 years ago.

It’s very easy to look at Carrowkeel 534, become smitten, and assume that this person was your ancestor.

By Shane Finan – Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=35098411

It’s especially easy if you WANT that person to be your ancestor. Carrowkeel 534 was buried in a passage tomb in County Sligo, Ireland. I’ve been there.

However, don’t let your emotions get involved – at least not yet.

This is the first example of the steps that determine that these remains are NOT YOUR ANCESTOR.

  • Carrowkeel 534 was a male, and we all know that males do not pass on their mitochondrial DNA. Well, that’s an inconvenient fact.😊
  • There are two sets of X2b4 remains in Ancient Connections. Carrowkeel 534 remains are about 4600-5000 years old, and your common ancestor with them lived about 5000 years ago. However, Radegonde was French and migration from Ireland to France is not typical.
  • The other set of X2b4 remains, Ladoga 16, lived more recently, between the years of 900 and 1200 (or 800-1100 years ago), but they are found in Russia.
  • Radegonde’s parent haplogroup, X2b4d’g was born about 3700 years ago, which excludes the Russian remains from being Radegonde’s direct ancestor.
  • Radegonde’s common ancestor with both these sets of remains lived about 5000 years ago, but these remains were not found even close to each other.

In fact, these remains, if walking, are about 3299 km (2049 miles) apart, including two major water crossings.

  • Given that Radegonde is probably French, finding her ancestor around 5000 years ago in an Irish passage tomb in County Sligo, or in a location east of St. Petersburg, is extremely unlikely.

What IS likely, though, is that X2b4d’g descendants of your common ancestor with both sets of remains, 5000 years ago, went in multiple directions, meaning:

  • Radegonde’s ancestor found their way to France and along the way incurred the mutations that define X2b4d’g and X2b4g by the year 1600 when she lived, or about four hundred years ago.
  • Another X2b4 descendant found their way to what is today Ireland between 4600 and 5000 years ago
  • A third X2b4 descendant found their way to Russia between 800-1100 years ago, and 5000 years ago

If any question remains about the genesis of Radegonde’s ancestors being Native, Ancient Connections disproves it – BUT – there’s still an opportunity for misunderstanding, which we’ll see in a few minutes.

Ancient Connections Analysis Chart

I’ve created an analysis chart, so that I can explain the findings in a logical way.

Legend:

  • Hap = Haplogroup
  • M=male
  • F=female
  • U=unknown

Please note that ancient samples are often degraded and can be missing important mutations. In other words, the tree placement may be less specific for ancient samples. Every ancient sample is reviewed by FamilyTreeDNA’s genetic anthropologist before it’s placed on the tree.

Ancient samples use carbon dating to determine ages. Sometimes, the carbon date and the calculated haplogroup age are slightly “off.” The haplogroup age is a scientific calculation based on a genetic clock and is not based on either genealogy or ancient burials. The haplogroup age may change as the tree matures and more branches are discovered.

I’m dividing this chart into sections because I want to analyze the findings between groups.

The first entry is the earliest known ancestor of the current lineage – Radegonde Lambert, who was born about 1621, or roughly 400 years ago. I’ve translated all of the years into “years ago” to avoid any confusion.

If you wish to do the same, with CE (Current or Common Era) dates, subtract the date from 2000. 300 CE= (2000-300) or1700 years ago. With BCE dates, add 2000 to the BCE number. 1000 BCE= (1000+2000) or 3000 years ago.

Connection Identity Age Years Ago Location & Cultural Group Hap Hap Age Years Ago Shared Hap Shared Hap Age Years Ago
Radegonde Lambert (F) 400 France or Canada -Acadian X2b4g 1700 X2b4 5000
Carrowkeel 534 (M) 4600-5100 Sligo, Ireland – Neolithic Europe X2b4 5000 X2b4 5000
Ladoga 16 (M) 800-1100 Ladoga, Russia Fed – Viking Russia X2b4 5000 X2b4 5000
  • Age Years Ago – When the Ancient Connection lived
  • Hap Age Years Ago – When the haplogroup of the Ancient Connection (X2b4) originated, meaning was born
  • Shared Hap Age Years Ago – When the Shared Ancestor of everyone in the Shared Haplogroup originated (was born)

In this first section, the haplogroup of the Ancient Connections and the Shared Haplogroup is the same, but that won’t be the case in the following sections. Radegonde Lambert’s haplogroup is different than her shared haplogroup with the Ancient Connections.

Let’s assume we are starting from scratch with Radegonde.

The first question we wanted to answer is whether or not Radegonde is European, presumably French like the rest of the Acadians, or if she was Native. That’s easy and quick.

Native people crossed Beringia, arriving from Asia someplace between 12,000 and 25,000 years ago in multiple waves of migration that spread throughout both North and South America.

Therefore, given that the first two samples, Carrowkeel 534 and Ladoga 16, share haplogroup X2b4, an upstream haplogroup with Radegonde Lambert, and haplogroup X2b4 was formed around 5000 years ago, the answer is that Radegonde’s X2b4 ancestor, whoever that was, clearly lived in Europe, NOT the Americas.

According to Discover, Haplogroup X2b4:

  • Was formed about 5000 years ago
  • Has 16 descendant haplogroups
  • Has 29 unnamed lineages (haplotype clusters or individuals with no match)
  • Includes testers whose ancestors are from 23 countries

The Country Frequency map shows the distribution of X2b4, including all descendant haplogroups. Please note that the percentages given are for X2b4 as a percentage of ALL haplogroups found in each colored country. Don’t be misled by the relative physical size of the US and Canada as compared to Europe.

The table view shows the total number of self-identified locations of the ancestors of people in haplogroup X2b4 and all downstream haplogroups.

The Classic Tree that we looked at earlier provides a quick view of X2b4, each descendant haplogroup and haplotype cluster, and every country provided by the 331 X2b4 testers.

For the X2b4 Ancient Connections, we’ve already determined:

  • That Radegonde’s ancestors were not Native
  • Carrowkeel 534 is a male and cannot be Radegonde’s ancestor. It’s extremely likely that Carrowkeel 534’s mother is not Radegonda’s ancestor either, based on several factors, including location.
  • Based on dates of when Ladoga 16 lived, and because he’s a male, he cannot be the ancestor of Radegonde Lambert.

Radegonda’s haplogroup was formed long before Ladoga 16 lived. Each Ancient Connection has this comparative Time Tree if you scroll down below the text.

  • Both Carrowkeel and Ladoga share an ancestor with our tester, and Radegonde, about 5000 years ago.

Think about how many descendants the X2b4 ancestor probably had over the next hundreds to thousands of years.

  • We know one thing for sure, absolutely, positively – X2b4 testers and descendant haplogroups live in 32 countries. People migrate – and with them, their haplogroups.

What can we learn about the genealogy and history of Radegonde Lambert and her ancestors?

We find the same haplogroup in multiple populations or cultures, at different times and in multiple places. Country boundaries are political and fluid. What we are looking for are patterns, or sometimes, negative proof, which is often possible at the continental level.

X2b4, excluding downstream haplogroups, is found in the following locations:

  • Bulgaria
  • Canada (2)
  • Czech Republic
  • England (2)
  • Finland (2)
  • France (3)
  • Germany (4)
  • Portugal
  • Scotland (2)
  • Slovakia (2)
  • Sweden (2)
  • UK (2)
  • Unknown (11)
  • US (2)

Note that there are three people in France with haplogroup X2b4 but no more refined haplogroup.

Looking at X2b4’s downstream haplogroups with representation in France, we find:

  • X2b4a (none)
  • X2b4b (none)
  • X2b4b1 (1)
  • X2b4d’g (none)
  • X2b4d (none)
  • X2b4g (24) – many from Radegonde’s line
  • X2b4e and subgroups (none)
  • X2b4f (none)
  • X2b4j and subgroups (none)
  • X2b4k (none)
  • X2b4l (1)
  • X2b4m (none)
  • X2b4n and subgroups (none)
  • X2b4o (none)
  • X2b4p (none)
  • X2b4r (none)
  • X2b4+16311 (none)

I was hoping that there would be an Ancient Connection for X2b4, X2b4d’g, or X2b4g someplace in or even near France – because that makes logical sense if Radegonde is from France.

All I can say is “not yet,” but new ancient sites are being excavated and papers are being released all the time.

Ok, so moving back in time, let’s see what else we can determine from the next set of Ancient Connections. Haplogroup X2b1”64 was formed about 5050 years ago.

Connection Identity Age Years Ago Location & Cultural Group Hap Hap Age Years Ago Shared Hap Shared Hap Age Years Ago
Radegonde Lambert (F) 400 France or Canada X2b4g 1700
Carrowkeel 534 (M) 5100-4600 Sligo, Ireland – Neolithic Europe X2b4 5000 X2b4 5000
Ladoga 16 (M) 800-1100 Ladoga, Russia Fed – Viking Russia X2b4 5000 X2b4 5000
Parknabinnia 186 (M) 5516-5359 Clare, Ireland – Neolithic Europe X2b1”64 5516-5259 X2b1”64 Before 5050 years ago
Rössberga 2 (M) 5339-5025 Vastergotland, Sweden – Funnel Beaker X2b1”64 5516-5259 X2b1”64 Before 5050
Rössberga 29 (M) 5366-5100 Vastergotland, Sweden – Funnel Beaker and Early Plague X2b1”64 5516-5259 X2b1”64 Before 5050
Rössberga 38 (M) 5340-5022 Vastergotland, Sweden – Funnel Beaker X2b1”64 5516-5259 X2b1”64 Before 5050
Monte Sirai 797263 (U) 2600-2400 Monte Sirai, Italy (Sardinia) – Phoenicians X2b35a1 3350 X2b1”64 5050
Bogovej 361 (F) 1000-1100 Lengeland, Denmark – Viking Denmark X2b1”64 5516-5259 X2b1”64 5050
Ladoga 410 (M) 800-1000 Leningrad Oblast, Russia – Viking Russia X2b1”64 5516-5259 X2b1”64 5050

Our first group ended with haplogroup X2b4, and our second group consists of haplogroup X2b1”64, the parent haplogroup of X2b4. X2b1”64 is a significantly larger haplogroup with many downstream branches found throughout Europe, parts of western Asia, the Levant, India, and New Zealand (which probably reflects a colonial era settler). The Country Frequency Map and Table are found here.

X2b1”64 is just slightly older than X2b4, but it’s much more widespread, even though they were born about the same time. Keep in mind that haplogroup origination dates shift as the tree is developed.

  • These seven individuals who share X2b1”64 as their haplogroup could be related to each other individually, meaning their MRCA, anytime between when they lived and when their haplogroup was formed.
  • The entire group of individuals all share the same haplogroup, so they all descend from the one woman who formed X2b1”64 about 5050 years ago. She is the shared ancestor of everyone in the haplogroup.

One X2b4 and one X2b1”64 individual are found in the same archaeological site in Russia. Their common ancestor would have lived between the time they both lived, about 800 years ago, to about 5000 years ago. It’s also possible that one of the samples could be incomplete.

A second X2b1”64 Ancient Connection is found in the Court Tomb in County Clare, Ireland, not far from the Carrowkeel 534 X2b4 site.

However, Monte Sirai is fascinating, in part because it’s not found near any other site. Monte Sirai is found all the way across France, on an island in the Tyrrhenian Sea.

It may be located “across France” today, but we don’t know that the Phoenician Monte Sirai site is connected with the Irish sites. We can’t assume that the Irish individuals arrived as descendants of the Monte Sirai people, even though it would conveniently fit our narrative – crossing France. Of course, today’s path includes ferries, which didn’t exist then, so if that trip across France did happen, it could well have taken a completely different path. We simply don’t know and there are very few samples available.

Three Ancient Connections are found in the Rössberga site in Sweden and another in  Denmark.

Adding all of the Ancient sites so far onto the map, it looks like we have two clusters, one in the northern latitudes, including Denmark, Sweden, and Russia, and one in Ireland with passage burials, plus one single Connection in Monte Sirai.

If I were to approximate a central location between all three, that might be someplace in Germany or maybe further east. But remember, this is 5000 years ago and our number of samples, as compared to the population living at the time is EXTREMELY LIMITED.

Let’s move on to the next group of Ancient Connections, who have different haplogroups but are all a subset of haplogroup X2.

Identity Age Years Ago Location & Cultural Group Hap Hap Age Years Ago Shared Hap Shared Hap Age Years Ago
Radegonde Lambert (F) 400 France or Canada X2b4g 1700
Carrowkeel 534 (M) 5100-4600 Sligo, Ireland – Neolithic Europe X2b4 5000 X2b4 5000
Ladoga 16 (M) 800-1100 Ladoga, Russia Fed – Viking Russia X2b4 5000 X2b4 5000
Parknabinnia 186 (M) 5516-5359 Clare, Ireland – Neolithic Europe X2b1”64 5516-5259 X2b1”64 Before 5050
Ross Rössberga 2 (M) 5339-5025 Vastergotland, Sweden – Funnel Beaker X2b1”64 5516-5259 X2b1”64 Before 5050
Rössberga 29 (M) 5366-5100 Vastergotland, Sweden – Funnel Beaker and Early Plague X2b1”64 5516-5259 X2b1”64 Before 5050
Rössberga 38 (M) 5340-5022 Vastergotland, Sweden – Funnel Beaker X2b1”64 5516-5259 X2b1”64 Before 5050
Monte Sirai 797263 (U) 2600-2400 Monte Sirai, Italy (Sardinia) – Phoenicians X2b35a1 3350 X2b1”64 5050
Bogovej 361 (F) 1000-1100 Lengeland, Denmark – Viking Denmark X2b1”64 5516-5259 X2b1”64 5050
Ladoga 410 (M) 800-1000 Leningrad Oblast, Russia – Viking Russia X2b1”64 5516-5259 X2b1”64 5050
Barcin 31 (M) 8236-8417 Derekoy, Turkey – Neolithic Anatolia Ceramic X2m2’5’7^ 9200 X2b”aq 13,000
Abasar 55 (M) 500-800 Abasár Bolt-tető, Abasar, Hungary – Medieval Hungary X2m1e 5350 X2b”aq 13,000
Gerdrup 214 3779-3889 Gerdrup, Sealand, Denmark – Middle Bronze Age X2c1 3400 X2+225 13,000
Sweden Skara 275 800-1100 Varnhem, Skara, Sweden – Viking Sweden X2c1 3400 X2+225 13,000
Kopparsvik 225 950-1100 Gotland, Sweden – Viking Sweden X2z 5650 X2+225 13,000
Sandomierz 494 900-1100 Sandomierz, Poland – Viking Poland X2c2b 1650 X2+225 13,000
Kennewick man 8390-9250 Kennewick, Washington – Native American X2a2’3’4^ 10,450 X2 13,000
Roopkund 39 80-306 Roopkund Lake, Uttarakhand, India – Historical India X2d 13,000 X2 13,000

The next several Ancient Connections have haplogroups that are a subgroup of haplogroup X2. These people lived sometime between 500 years ago in Hungary, and 8390-9250 years ago when Kennewick Man lived in the present-day state of Washington in the US. Kennewick Man merits his own discussion, so let’s set him aside briefly while we discuss the others.

The important information to be gleaned here isn’t when these people lived, but when Radegonde shared a common ancestor with each of them. The shared haplogroup with all of these individuals was born about 13,000 years ago.

Looking at the map again, and omitting both X2 samples, we can see that the descendants of that shared ancestor 13,000 years ago are found more widely dispersed.

Including these additional burials on our map, it looks like we have a rather large Swedish and Viking cluster, where several of the older burials occurred prior to the Viking culture. We have a Southeastern Europe cluster, our two Irish tomb burials, and our remaining single Monte Sirai Phoenician burial on the island of Sardinia.

Stepping back one more haplogroup to X2, which was born about the same time, we add a burial in India, and Kennewick Man.

The Migration Map

The Migration map in Discover provides two different features.

  • The first is the literal migration map for the various ancestral haplogroups as they migrated out of Africa, if in fact yours did, culminating in your base haplogroup. In this case, the base haplogroup is X2, which is shown with the little red circle placed by FamilyTreeDNA. I’ve added the red squares, text and arrows for emphasis.
  • The second feature is the mapped Ancient Connections, shown with little brown trowels. Clicking on each one opens a popup box.

After haplogroup X2 was formed, it split into haplogroups X2a and X2b.

The X2a group, Kennewick Man’s ancestors, made their way eastward, across eastern Russia to Beringia where they crossed into the Americas.

They either crossed Beringia, follow the Pacific coastline, or both, eventually making their way inland, probably along the Hood River, to where Kennewick Man was found some 2,800 years later on the banks of the Kennewick River.

The X2b group made their way westward, across western Europe to a location, probably France, where Radegonde Lamberts’ ancestors lived, and where Radegonde set sail for Nova Scotia.

After being separated for nearly 13,000 years, the descendants of the single woman who founded haplogroup X2 and lived someplace in central Asia around 13,000 years ago would find themselves on opposite coasts of the same continent.

So, no, Radegonde Lambert was not Native American, but her 600th matrilineal cousin or so, Kennewick Man, absolutely was.

Radegonde Lambert and Kennewick Man

Here’s where confirmation bias can rear its ugly head. If you’re just scanning the Ancient Connections and see Kennewick Man, it would be easy to jump to conclusions, leap for joy, slap a stamp of “confirmed Native American” on Radegonde Lambert, and never look further. And if one were to do that, they would be wrong.

Let’s work through our evaluation process using Discover.

Radegonde Lambert and Kinnewick Man, an early Native American man whose remains were found Kennewick, Washington in 1996, are both members of the broader haplogroup X2. Kennewick Man lived between 8290 and 9350 years ago, and their shared ancestor lived about 13,000 years ago – in Asia, where mitochondrial haplogroup X2 originated. This is the perfect example of one descendant line of a haplogroup, X2 in this case, going in one direction and a second one traveling in the opposite direction.

Two small groups of people were probably pursuing better hunting grounds, but I can’t help but think of a tundra version of the Hatfields and McCoys and cousin spats.

“I’m going this way. There are better fish on that side of the lake, and I won’t have to put up with you.”

“Fine, I’m going that way. There are more bears and better hunting up there anyway.”

Their wives, who are sisters, “Wait, when will I ever see my sister again?”

One went east and one went west.

X2a became Native American and X2b became European.

Looking back at our information about Kennewick Man, his haplogroup was born significantly before he lived.

He was born about 8390-9250 years ago, so let’s say 8820 years ago, and his haplogroup was born 10,500 years ago, so about 1680 years before he lived. That means there were many generations of women who carried that haplogroup before Kennewick Man.

Let’s Compare

Discover has a compare feature.

I want to Compare Radegonde Lambert’s haplogroup with Kennewick Man’s haplogroup X2a2’3’4^.

The Compare tool uses the haplogroup you are viewing, and you enter a second haplogroup to compare with the first.

The ancestral path to the shared ancestor, meaning their shared haplogroup, is given for each haplogroup entered. That’s X2 in this case. Then, from the shared haplogroup back in time to Mitochondrial Eve.

I prefer to view this information in table format, so I created a chart and rounded the haplogroup ages above X2.

Hap Age – Years Ago Radegonde’s Line Shared Ancestors and Haplogroups Kennewick’s Line Hap Age – Years Ago
143,000 mt-Eve
130,000 L1”7
119,000 L2”7
99,000 L2’3’4’6
92,000 L3’4’6
73,500 L3’4
61,000 L3
53,000 N
53,000 N+8701
25,000 X
22,500 X1’2’3’7’8
13,000 X2 – Asia
13,000 X2+225 X2a 10,500
12,900 X2b”aq X2a2’3’4^ 10,400 Kennewick Man born c 8800 years ago
11,000 X2b
5,500 X2b1”64
5,000 X2b4
1,900 X2b4d’g
Radegonde Lambert born c 1661 – 400 years ago 1,700 X2b4g

More Ancient Connections

Radegonde Lambert’s matrilineal descendants have an additional dozen Ancient Connections that are found in upstream haplogroup N-8701. Their shared ancestors with Radegonde reach back to 53,000 years ago in a world far different than the one we inhabit today. I’m not going to list or discuss them, except for one.

Identity Age Years Ago Location & Cultural Group Hap Hap Age Years Ago Shared Hap Shared Hap Age Years Ago
Radegonde Lambert (F) 400 France or Canada X2b4g 1700
Carrowkeel 534 (M) 5100-4600 Sligo, Ireland – Neolithic Europe X2b4 5000 X2b4 5000
Ladoga 16 (M) 800-1100 Ladoga, Russia Fed – Viking Russia X2b4 5000 X2b4 5000
Parknabinnia 186 (M) 5516-5359 Clare, Ireland – Neolithic Europe X2b1”64 5516-5259 X2b1”64 Before 5050
Rössberga 2 (M) 5339-5025 Vastergotland, Sweden – Funnel Beaker X2b1”64 5516-5259 X2b1”64 Before 5050
Rössberga 29 (M) 5366-5100 Vastergotland, Sweden – Funnel Beaker and Early Plague X2b1”64 5516-5259 X2b1”64 Before 5050
Rössberga 38 (M) 5340-5022 Vastergotland, Sweden – Funnel Beaker X2b1”64 5516-5259 X2b1”64 Before 5050
Monte Sirai 797263 (U) 2600-2400 Monte Sirai, Italy (Sardinia) – Phoenicians X2b35a1 3350 X2b1”64 5050
Bogovej 361 (F) 1000-1100 Lengeland, Denmark – Viking Denmark X2b1”64 5516-5259 X2b1”64 5050
Ladoga 410 (M) 800-1000 Leningrad Oblast, Russia – Viking Russia X2b1”64 5516-5259 X2b1”64 5050
Barcin 31 (M) 8236-8417 Derekoy, Turkey – Neolithic Anatolia Ceramic X2m2’5’7^ 9200 X2b”aq 13,000
Abasar 55 (M) 500-800 Abasár Bolt-tető, Abasar, Hungary – Medieval Hungary X2m1e 5350 X2b”aq 13,000
Gerdrup 214 3779-3889 Gerdrup, Sealand, Denmark – Middle Bronze Age X2c1 3400 X2+225 13,000
Kopparsvik 225 950-1100 Gotland, Sweden – Viking Sweden X2z 5650 X2+225 13,000
Sandomierz 494 900-1100 Sandomierz, Poland – Viking Poland X2c2b 1650 X2+225 13,000
Sweden Skara 275 800-1100 Varnhem, Skara, Sweden – Viking Sweden X2c1 3400 X2+225 13,000
Kennewick man 8390-9250 Kennewick, Washington – Native American X2a2’3’4^ 10,450 X2 13,000
Roopkund 39 80-306 Roopkund Lake, Uttarakhand, India – Historical India X2d 13,000 X2 13,000
Ranis 10 43,500-47,000 Ranis, Germany – LRJ Hunger Gatherer N3’10 53,000 N+8701 53,000
Zlatý kůň woman 47,000 Czech Republic – N+8701 53,000 N+8701 53,000

Zlatý kůň Woman

Zlatý kůň Woman lived some 43,000 years ago and her remains were discovered in the Czech Republic in 1950.

Believed to be the first anatomically modern human to be genetically sequenced, she carried about 3% Neanderthal DNA. Europeans, Asians and indigenous Americans carry Neanderthal DNA as well.

Unlike many early remains, Zlatý kůň Woman’s facial bones have been scanned and her face approximately reconstructed.

There’s something magical about viewing a likeness of a human that lived more than 40,000 years ago, and to whom I’m at least peripherally related.

Like all other Ancient Connections, it’s unlikely that I descend from Zlatý kůň Woman herself, but she is assuredly my very distant cousin.

What else do we know about Zlatý kůň Woman? Quoting from her Ancient Connection:

She lived during one of the coldest periods of the last ice age, surviving in harsh tundra conditions as part of a small hunter-gatherer group. She died as a young adult, though the cause of death remains unknown.

Her brain cavity was larger than that of modern humans in the comparative database, another trait showing Neanderthal affinity. While the exact colors of her features cannot be determined from available evidence, researchers created both a scientific grayscale model and a speculative version showing her with dark curly hair and brown eyes.

Zlatý kůň Woman may or may not have direct descendants today, but her haplogroup ancestors certainly do, and Radegonde Lambert is one of them, which means Radegonde’s matrilineal ancestors and descendants are too.

Ancient Connections for Genealogy

While Ancient Connections are fun, they are more than just amusing.

You are related through your direct matrilineal (mitochondrial) line to every one of your mtDNA Discover Ancient Connections. Everyone, males and females, can take a mitochondrial DNA test.

I find people to test for the mitochondrial DNA of each of my ancestral lines – like Radegonde Lambert, for example. I wrote about various methodologies to find your lineages, or people to test for them, in the article, Lineages Versus Ancestors – How to Find and Leverage Yours.

Radegonde’s mitochondrial DNA is the only key I have into her past, both recent and distant. It’s the only prayer I have of breaking through that brick wall, now or in the future.

Interpreted correctly, and with some luck, the closer Ancient Connections can provide genealogical insight into the origins of our ancestors. Not just one ancestor, but their entire lineage. While we will never know their names, we can learn about their cultural origins – whether they were Vikings, Phoenicians or perhaps early Irish buried in Passage Graves.

On a different line, an Ancient Connection burial with an exact haplogroup match was discovered beside the Roman road outside the European town where my ancestral line was believed to have been born.

Ancient Connections are one small glimpse into the pre-history of our genetic line. There are many pieces that are missing and will, in time, be filled in by ancient remains, Notable Connections, and present-day testers.

Check your matches and your Ancient Connections often. You never know when that magic piece of information you desperately need will appear.

What is waiting for you?

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New Mitotree Haplogroups and How to Utilize Them for Genealogy

Have you received a new Mitotree haplogroup? Or maybe you didn’t? Are you wondering why you might not have received a new haplogroup? How do the new haplogroups work anyway? And how do you work with them?

Great questions!

Approximately 75% of full sequence testers received a new haplogroup with the Mitotree Beta release, which means that about 25% did not. Keep in mind that new sequences are being added to the database, so the tree will be sprouting new haplogroups with each subsequent release.

Check For Your New Haplogroup

Click on any image to enlarge

Sign in to your account at FamilyTreeDNA and look at the Badges in the bottom right corner of your page.

Your Beta haplogroup is your new Mitotree haplogroup, and your Legacy haplogroup is your old one – prior to Mitotree. They may be the same. My haplogroup, shown above, did not change.

This is a good place to note that the tree is not “done,” yet, nor will it ever be. New samples are added daily as more people test and as academic samples from published papers are added to the database as well. Additionally, FamilyTreeDNA is tweaking the algorithm, so the tree branching structure may change from time to time.

When your haplogroup changes, you’ll receive a notification email.

Some people’s haplogroup will remain the same. There can be several reasons why you might not have received a new haplogroup.

Before we discuss that, I’d like to stress that your haplogroup remaining the same isn’t exactly a bad thing because there is SO MUCH new content for everyone. It’s like receiving a whole new book about your mother’s direct matrilineal line.

mtDNA Discover Offers 13 New Reports for Everyone

MtDNA Discover was released with the new Mitotree, and it includes a dozen new reports for EVERY haplogroup.

Discover is available publicly, and also through your FamilyTreeDNA dashboard which provides a customized experience for mtFull testers with additional information that is not available in the free version.

Think of these Discover reports as chapters in your personal book – all about you and your matrilineal ancestors.

The Discover reports are provided in addition to the tools in the mtDNA Results and Tools section of your dashboard on FamilyTreeDNA.

There’s something for everyone, even if you don’t have a new haplogroup. There’s certainly new information that will help with your genealogy and with understanding the history and ancestral journey of your mother’s direct line maternal ancestors.

Three Reasons Why You Might Not Receive a New Haplogroup

Ok, so why might you not have received a new haplogroup?

The first reason that you might not have received a new haplogroup assignment is the simplest. The new tree is only updated periodically.

After your results are returned, and before the next Mitotree version is available, your Mitotree haplogroup Badge will show as “Analyzing.”

If one of your matches is waiting for a new haplogroup, their Mitotree Haplogroup will show as “Pending Analysis.”

There is no published tree-update schedule, but you’ll receive your new haplogroup soon.

However, you can probably determine your new haplogroup quite easily. If you have any exact matches on your mtDNA Match page, their haplogroup will be your haplogroup as well, so check your full sequence mtDNA Matches on your dashboard for a hint.

For, example, here’s one of my exact matches with their haplogroup.

The second reason you might not have a new haplogroup assignment is that you may not have taken the full sequence mitochondrial DNA test – mtFull.

Only testers with full sequence test results can receive an updated haplogroup, because the full mitochondria needs to be tested. The older HVR1/HVR2 Plus tests only tested a fraction of the full sequence – around 1000 locations of the 16,569 locations tested in the full sequence test.

If you have only taken the HVR1 or HVR1/HVR2 level test, you will only have one badge, and it will say “Predicted.”

The haplogroup for the Plus test is predicted at a high level based on those 1000 locations, while the full sequence test tests the entire mitochondria and uses all locations to confirm your most granular and detailed haplogroup possible.

On your dashboard, if both the Plus and Full icons are pink, you have taken the mtFull test. If the “Full” is grey, you have not. You can click on that grey button to upgrade.

You can also navigating to on Add Ons and Upgrades in the top bar to upgrade to the full sequence test.

The third reason why someone might not have received a new haplogroup assignment is if they didn’t match with anyone else who has the same mutations, or variants, for a particular haplogroup.

In other words, if my mitochondrial DNA has had a mutation or two since my assigned haplogroup was formed and no one else has tested that has those exact same mutations, there’s no one else to form a new haplogroup with, but there might be in the future as additional people test and the tree continues to grow.

Think of those additional mutations, called Private Variants, as foundation blocks, or haplogroup seeds since they are still private to you, and not yet used for a haplogroup.

It’s easy to see if you have any Private Variants by clicking on Discover on your mitochondrial dashboard.

Scientific Details – Private Variants, Building Blocks, Haplogroup Seeds

If you have taken the full sequence test, click through to mtDNA Discover from your dashboard. If you aren’t signed in and click through from your dashboard, you won’t be able to see your variants or other information customized for you.

Navigate to Scientific Details, then click on the Variants tab.

Click on image to enlarge

Be sure that “Show private variants” is toggled to “on,” which is blue with a checkmark.

At the very top, you’ll see two things:

  1. Your haplogroup, which is indicated by the solid pink square.
  2. An F number followed by your private variants, if any, and if so, which ones.

I have no private variants or haplogroup seeds available to form a new haplogroup, so I have no ability to receive a more refined haplogroup.

Haplotype Clusters

However, I’m NOT out of luck, because I have something else – a Haplotype Cluster, indicated by having an F#. My Haplotype Cluster is F1752176 and is indicated by the pink outlined box.

I wrote about haplotype clusters in the article, Mitochondrial DNA: What is a Haplotype Cluster and How Do I Find and Use Mine?.

In a nutshell, haplogroups are only formed around reliable, relatively stable mutations, meaning those that are reliable and don’t tend to randomly mutate back and forth.

You may match exactly with a group of other people who share the same haplogroup, PLUS the same unstable mutations that don’t qualify to become haplogroup-defining.

Those groups of two or more people who match exactly on all mutations are members of the same  Haplotype Cluster – and Haplotype Clusters can be INCREDIBLY genealogically useful. In fact, let me go out on a limb here and say that I think they are even more genealogical useful than haplogroups, although both have their strengths. Let’s look at a good example.

Using Haplogroups and Haplotype Clusters Together

My family member, Jim, had a surprise waiting for him in his mitochondrial DNA. When he received his new haplogroup, I took a look to see what new information might be forthcoming.

His legacy haplogroup was V, and his new Mitotree haplogroup is V216a2 which is significantly more refined.

Before Mitotree and Haplotype Clusters, there wasn’t much to differentiate him from his other matches.

Let’s take a look at JUST his genetic information before adding genealogy.

If I click on the Time Tree for haplogroup V216a2, I see two testers with no cluster, meaning no one matches them exactly, and Jim’s cluster number F9712482.

Keep in mind that Jim might not match everyone in his haplogroup – only people at or beneath the matching threshold.

Jim’s new haplogroup, V216a2 was formed about 1056 CE, or about 975 years ago. Note that as the tree changes and becomes more refined, haplogroup formation dates change too. A haplogroup’s birth date is an approximate year when the mutations occurred that define that haplogroup, based on surrounding mutations and mutation rates.

Many people look at a haplogroup, especially one with a birth date of, say, 1056 CE, which is long before the formation of surnames, shrug their shoulders, and give up.

Don’t. Do. That.

So, let me say this as loudly as possible.

A haplogroup’s most recent common ancestor is NOT the EKA (earliest known ancestor) with any individual match. It’s the approximate date when ALL of the people with this haplogroup share a common ancestor.

When looking at haplogroups, don’t let locations thrown you. Keep in mind that country boundaries are fluid. What was at one time Hungary could be Germany or Romania or something else just a few years earlier or later. So don’t discount that information either. Think regions and take into consideration that people move around – and some people enter incorrect genealogy/location information.

Your common ancestor with the people, individually, who share your haplogroup,  is sometime between the haplogroup formation date and today. Everything else is a clue. 

Think about it this way. You share a haplogroup with your mother, and while you are both descended from the woman who lived when your haplogroup was formed – your most recent ancestor with that haplogroup is your mother – not the woman 975 years ago. Your most recent common ancestor (MRCA) with your mother and her sister is your grandmother – a lot closer in time than 1056 CE. 1056 CE the most recent common ancestor (MRCA) date for everyone in the haplogroup, not between you and any one person in particular. The MRCA date for you plus another person is sometime between now and 1056 CE.

So, let’s take a look at Jim’s results.

Finding Jim’s Gold Nugget

Jim has 27 coding region matches, of which six share both his new haplogroup, V216a2, AND Haplotype Cluster F9712482. His other matches are split between three related haplogroups, and multiple haplotype clusters.

Most of his family, meaning three of his grandparents, were from eastern Europe, meaning Germany, Hungary or the Austro-Hungarian empire as it was recorded in American records. Many genealogical records no longer exist in that region, or if they do, you have to know exactly where to look.

We were brick-walled with Jim’s matrilineal great-grandmother, Sophia Smith, who was born about 1877 and seemed to appear out of thin air.

Thanks to the new haplogroups, combined with Haplogroup Clusters, I knew to focus on his matches in this order:

  • Same haplogroup plus same Haplotype Cluster
  • Same haplogroup plus different Haplotype Cluster, because clusters are built around identical but less reliable mutations
  • Related haplogroup – this is unlikely to yield direct genealogical results, but can be very useful in terms of origins

Of Jim’s exact matches with the same Haplotype Cluster, three showed an earliest known ancestor (EKA) and three did not. Three provided a tree, and three did not. Of the trees, one was private and the other two provided no useful insight.

Of the people who provided EKA information, one EKA matches their tree information, one conflicts with their tree. After viewing their tree, it appears that they did not understand that the mitochondrial EKA is the most distant ancestor in your mother’s direct maternal line. They listed someone in their grandmother’s paternal line.

I find this easiest to deal with if I organize the research in a chart for each match.

Match # Earliest Known Ancestor EKA Location Tree Comment
#1 No No No
#2 No No No
#3 No No Yes – Private
#4 Yes – only one name “Egan” with brith and death dates Ireland Yes – Egan is surname of their grandmother EKA person listed tracks up wrong line in tree
#5 Yes Hungary No Elizabeth Schmidt Hornung b1888 d 1930
#6 Yes No Yes – matches EKA Ancestor born NC in 1811, no common names or location

Match #5 provided an EKA, but no tree, showed a country of origin as Hungary, and the identity of her EKA as “Elizabeth Schmidt Hornung b.1888 and d.1930.”

Hmmm…three things of interest here:

  • The location of Hungary, even though the oral history in Jim’s family said his great-grandmother was a Smith from the US, maybe New York. Jim’s family, including Sophia’s husband, was Eastern European. Remember, I couldn’t find any early records for Sophia Smith.
  • Smith is the anglicized version of Schmidt.
  • Hornung may be a married name.

I’m a genealogist, and Jim’s match had provided enough information that I was able to identify her ancestor, Elizabeth Schmidt, and find additional information.

Sure enough, Elizabeth Schmidt immigrated as an adult by herself, married Karl Hornung in Richland County, Ohio, the same location where Jim’s family was living. That information led me to another record, identifying a brother whose marriage license application provided their parents. Elizabeth’s parents were Ignatius Schmidt and Catherine Schlowe, and her sister was Sophia Schmidt, Jim’s great-grandmother. Deeper digging suggests that Ignatius and Catherine were from Timisoara in what is now Romania. I have been unable to confirm with birth, death or marriage records, but that part of Romania was part of the Austro-Hungarian Empire during that timeframe.

Immigration of siblings, alone, at different times after the 1910 census, without their parents, made this particularly difficult, as did cultural and language barriers – but mitochondrial DNA, and Jim’s Haplotype Cluster in particular, provided the key I needed.

Jim’s common ancestor with his Schmidt match is the birth date of Catherine Schlowe, which was probably about 1850 – NOT 1056 CE, which is the haplogroup formation date.

Don’t get discouraged by misinterpreting haplogroup origin information or missing genealogy information. All you need is that one good match. That gold nugget. Don’t forget that you can email your matches and ask for more information.

The Match Time Tree makes all of this easier.

Match Time Tree

The Match Time Tree shows match, haplogroup, location and Haplotype Cluster information all in one place.

It’s easy to use the Match Time Tree to view how all of your matches are grouped, along with their EKA, displayed together in one place.

Here are all of Jim’s matches. They were all originally haplogroup V, but now his matches have been divided into V216, V216a, V216a1, and V216a2 (Jim’s haplogroup).

I’ve obfuscated the names of his matches, but the EKA, when provided, is there. Each person is grouped into their haplotype cluster of exact matches, and the user-provided country of origin for their ancestor is shown by their profile photo.

Jim’s match with the descendant of Elizabeth Schmidt is indicated in the red boxes, and Jim has updated his own EKA and her country of origin.

Who is waiting for you in your match list?

Will extending and building out trees help?

Have you emailed your matches to see what additional information they can provide?

Female ancestors are sometimes the MOST difficult to find, often due to name changes  – so be sure to mine every possible avenue and don’t become discouraged if you don’t immediately see something “familiar.”

Every generation in a female lineage will probably carry a different surname and the match you need may not have researched as far back as your ancestor, or vice versa.

Don’t forget that autosomal matching can play an important role in confirming relationships.

But wait – there’s STILL more about Jim’s ancestors…

There’s Even More to Discover

There’s more to discover about Jim’s ancestors.

Jim’s Discover Ancient Connections tells me that 5200 years ago, Jim shared a common mitochondrial DNA ancestor with two Hungarian and a Slovakian Yamnaya cultural burial whose remains date to about 2800 BCE, or about 4800 years ago.

To be clear, the common haplogroup between Jim and all three burials dates to 5200 years ago, when their common haplogroup was formed, but the remains themselves are from about 4800 years ago – so only about 400 years difference between the haplogroup birth date and when those people lived, died and were buried.

How close are the remains to the location of Jim’s ancestor in Timisoara?

Using Google Maps, I placed the three Yamnaya burial locations (blue pins), plus Timisoara.

The two most distant points, Timisoara to Lesne, Slovakia, walking, is 393 km or 245 miles. The closest burial to Timisoara, located in Sárrétudvari, Hungary, is 157 km  or 119 miles.

So Jim’s ancestors remained in the same general area for someplace between 4,800 and 5,200 years. And, his great-grandmother was born not far from those burials. That alone is an INCREDIBLE find!

So, what happened to the people of the Yamnaya culture? I think we might have gained some insight into that question.

So, there’s even more to discover using Discover.

You don’t know what you don’t know about your matrilineal ancestors, so test your mitochondrial DNA at FamilyTreeDNA and break through those brick walls. I’ve already solved multiple long-standing mysteries and added generations to my own tree.

Plus, I really, REALLY want to know where every single ancestor “came from,” what culture they were a part of, and when. History is part of genealogy – and a part of our ancestral journey that we can’t reach any other way.

Fortunately, your matches, Scientific Details, Time Tree, Match Time Tree, and Ancient Connections help you visualize all of these various situations and aspects of your ancestor’s history, and evaluate your results.

Both haplogroups and Haplotype Clusters provide very fine degrees of granularity that were not previously available. MtDNA Discover adds a dozen new reports, and Ancient Connections allow you to time travel.

Let me know what you discover!

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Mitochondrial DNA: What is a Haplotype Cluster and How Do I Find and Use Mine?

A new feature called Haplotype Clusters was released with the new Mitotree and mtDNA Discover.

MtDNA Discover includes a dozen new reports for EVERY haplogroup. You can use the public version of Discover with any haplogroup.

However, there are additional included features for mtFull testers, and other information provided will be much more detailed and robust because the mtFull test is much more specific than any partial haplogroup.

If you have only taken the older partial-coverage HVR1 or HVR1/HVR2 tests at FamilyTreeDNA, you can sign in and upgrade, or if you have received a partial haplogroup from another source, you can take the mtFull test at FamilyTreeDNA.

OK, I’ve Taken the mtFull Test, So How Do I Access My Discover Reports?

Sign in to your FamilyTreeDNA account, then from your mtDNA dashboard, click through to Discover to access your Discover reports.

Discover reports are in addition to the tools in the mtDNA Results and Tools section of your dashboard on FamilyTreeDNA.

Definitions

Let’s start with some basic definitions.

  • Haplotype – Your individual DNA results at specific adjacent locations that are generally inherited together.

Other people may have the same haplotype as you. If they have mutations that you don’t have, or vice versa, then you have different haplotypes. People with the same haplotypes match exactly on whatever type of DNA is being discussed, such as Y-DNA or mitochondrial DNA, with no mutations or differences. Multiple people who match exactly are considered a Haplotype Cluster.

  • Haplogroup – A group of specific mutations that identify people who share a common genetic clan. Haplogroups, based on a series of mutations, can be traced forward and backward in time.

A haplogroup is a grouping of haplotypes with the same foundation mutations. You will share those mutations with other people in your haplogroup, but you may have other, different mutations that form your haplotype.

  • Other people will have the same haplogroup as you, because a group implies two or more.
  • You may or may not share a haplotype with other people. If you share the exact same haplotype with at least one other person, the two (or more) of you form a Haplotype Cluster

What is a Haplotype Cluster?

Haplotype Clusters are new and have been added to provide additional granularity to the new Mitotree, making results more genealogically useful.

In addition to your mitochondrial DNA haplogroup, you may also have a Haplotype Cluster if you took a full sequence mitochondrial DNA test, called the mtFull.

A mitochondrial DNA haplogroup, such as J1c2f for example, means that everyone within that haplogroup has the same foundation grouping of mutations. You may have additional mutations, or even some missing mutations, based on the older Phylotree Build 17, which was last updated in 2016.

Click to enlarge any image

To see your Extra and Missing Mutations in the Classic, or Phylotree build, on the FamilyTreeDNA mtDNA dashboard, click on “See More,” then on Mutations.

In the recently released Mitotree, which reconstructs the tree of humanity with more than 35,000 new branches, or haplogroups, many of those “extra” or “missing” mutations have been used in the definition of new haplogroups.

At FamilyTreeDNA, on your matches page, you’ll see your matches, like always. Matching has not changed.

You’ll notice that some are exact matches, and some may be “1 step” or more distant. That means they have one qualifying genetic mutation difference from you.

Some mutations have always been excluded from matching because they are unreliable. In my case, location 315.1C is one of those. You can read more about matching here. Matching has NOT been rerun with the release of the new Mitotree, but may be in the future.

The new Haplotype Clusters designate other people who you literally match exactly, with no differences – and no excluded marker locations.

So, let’s compare how I match people and what it means:

  • Haplogroup match – I match these people at the haplogroup level, which can reach back hundreds or even thousands of years ago. In addition, I may match them on both other relevant, reliable mutations, and/or unreliable mutations. On the current matching page, the mtDNA Haplogroup is the PhyloTree Build 17 haplogroup. Before Mitotree, matches to any other haplogroup were not displayed. Now, new haplogroups of my J1c2f matches, if they received a new haplogroup, are shown in the Mitotree Haplogroup column. My common ancestor with a match can have occurred anytime between when the haplogroup was formed and today.

Some people receive partial haplogroup level matches from other testing companies that also don’t include matching. A haplogroup match alone isn’t particularly useful except when it can eliminate a connection.

That’s why we need matching on the Matches page.

  • FamilyTreeDNA Matches Page Match – On the Matches page, I match these people at the haplogroup level as calculated based on Phylotree Build 17, as shown in the mtDNA Haplogroup Column at the Genetic Distance displayed. This means that I match them on the haplogroup markers PLUS possibly other markers.

My first match with Per, above, is listed as an exact match. Before Haplotype Clusters were introduced, I had no way of knowing if I matched him on all of my mutation locations, or just the ones that are NOT excluded from matching. But now I do.

My Haplotype Cluster number is F1752176. I know this because the little circle is checked and blue – meaning this person and I share both a haplogroup in the new Mitotree, and a Haplotype Cluster.

Ronald, above, is a match with a “1 step” Genetic Difference. I know for sure that I match him on the haplogroup markers. I also know that we don’t match on one non-excluded marker – but I have no idea which one. We may also match, or not, on some of the excluded markers. But we are not members of the same Haplotype Cluster. The blue circle is not checked.

You cannot be a member of more than one Haplotype Cluster, because everyone in a Haplotype Cluster must match exactly.

  • Haplotype Cluster – A Haplotype Cluster, if you have one, is a random F number assigned to people whose mitochondrial DNA matches exactly – and by exactly, I mean without excluding unstable or unreliable mutations.

You can see my Haplotype Cluster number, above, in the Mitotree Haplogroup column, in addition to my new Mitotree haplogroup – which is still J1c2f and did not change from the earlier version. In Mitotree, some people will receive new haplogroups, and some will not – based on your and other people’s mutations.

My match with Ronald is one step difference. Our haplogroup is the same, so that circle is checked, but Ronald belongs to a different Haplotype Cluster, so that circle is not checked, and he has a different F number. I can’t see his mutations that are different from mine, but I know he matches everyone else in his Haplotype Cluster exactly.

Let’s look at another example.

Click on any image to enlarge

Looking at my match list, I can see that beneath my matches’ haplogroup, which is the same as mine, F1752176 is checked and the checked circle is blue, which means that I share that Haplotype Cluster with those people. Everyone in that cluster has all of the same mutations in addition to the haplogroup-defining mutations, which is why both the haplogroup and haplotype circles are checked. I match both.

If I look at my Matches page, or the mtDNA Discover Time Tree, or Matches Time Tree, I can see that I have many exact haplotype matches, which means:

  • We all share haplogroup-defining mutations and
  • We match exactly on all other mutations as well

Before Haplotype Clusters were introduced, I had no way of knowing which of these people I matched exactly if no mutations were excluded.

To summarize, a Haplotype Cluster is a group of people who all match each other exactly within a haplogroup. People in Haplotype Clusters always match exactly, which INCLUDES mutations that are EXCLUDED from haplogroup formation and matching.

If you don’t match someone exactly, you’re not in the same Haplotype Cluster. You can either be in a different cluster, or no cluster at all if no one matches you exactly.

Everyone has a Haplotyupe Cluster number, but you will only be a member of a Haplotype Cluster if you have an exact match to at least one other person.

Don’t Ignore Other Clusters

The F number itself isn’t important. What is important is that Haplotype Clusters serve to focus your genealogy on that cluster first. However, understand that because the Haplotype Cluster does include unreliable or fast-mutating markers, it’s possible for you to share a more recent ancestor with people in a different cluster. It depends on the marker and the mutation, so don’t discount that possibility.

Who Can See Haplotype Cluster Mutations?

The only people who know the exact mutations of the people in a specific Haplotype Cluster are the members of that cluster – because they all match exactly.

If you scroll down your match list, you’ll notice that people, like Anastasia, who have a genetic distance of 1 step or greater have a different F Haplotype Cluster number, which is expected.

You may also notice that someone who is an “exact match” with you on the match list is assigned to a different Haplotype Cluster, such as Rose and Per. Rose is not in my Haplotype Cluster, but Per is, even though they are both “exact matches.”

Remember, “matching exactly” on the match list excludes unreliable mutation locations. Haplotype Clusters always match exactly and include all mutations. So, this tells me that I match Per on all mutation locations, regardless of their stability, and I match Rose on all stable locations, and we mismatch on at least one location that was excluded from matching.

However, the only people who know the exactly mutations of any other person are me and Per, because we both share a Haplotype Cluster. People in other clusters, or without a cluster, don’t know and can’t identify the mutations in clusters not their own.

  • The only thing I can tell about my match with Rose is that we don’t share one of the unreliable markers, because we are an “exact match” on the match list which excludes unstable markers. I have no idea whether I carry that unstable marker, or she does, or which marker it is.
  • The only thing I can tell about my match with Anastasia is that we don’t share at least one stable marker, because we are a “1-step” genetic distance, and we could also not share some of the unstable markers. I have no way of identifying those markers.
  • I know that I match Per exactly on all markers, including unstable or unreliable markers.

Included Versus Excluded Markers

Sometimes people who are listed as exact matches on your Matches page are assigned to different Haplotype Clusters. This is because mutations such as 309 and several others are included in Haplotype Clusters, but excluded from matching and haplogroup formation. The reason they are excluded is because they are sometimes unreliable – but they may be useful to your research. They aren’t always unreliable, but it varies on a case-by-case basis, including when the mutation occurred.

Location Haplogroup Formation Matching on Matches Page Haplotype Cluster
309 Excluded Excluded Included

Here’s an example using location 309. While some locations are excluded from matching, their inclusion in the formation of Haplotype Clusters may be very genealogically relevant to you – or perhaps not. That’s where genealogy research becomes important.

Haplotype Clusters give you the ability to focus your research on a specific group of people that you know do, in fact, match you exactly. Just keep in mind that some people in a different Haplotype Cluster, that don’t have a mutation at 309, for example, could have a closer common ancestor. That’s the nature of 309, 315 and other unstable SNPs, especially heteroplasmies, which tend to “come and go,” which I wrote about here. In other words, don’t ignore other Haplotype Clusters that appear on your match list – just begin with your own and evaluate using genealogy..

The Haplotype Cluster number itself isn’t important. What is important is that they serve to focus your genealogy efforts.

Where Else Can I Find My Haplotype Cluster

You can identify your Haplotype Cluster number by looking at your match list, as we have discussed, or by navigating to the Variants tab on the Scientific Details page.

On the variants tab, your haplogroup is marked with the solid red square, along with other information which I have truncated here.

Immediately above your haplogroup, you’ll see your Haplotype Cluster number, if you have one, along with any remaining private variants, aka mutations, that are haplogroup seeds and qualify to potentially become part of a haplogroup in the future.

In my case, this tells me that either all of my mutations are now included in a haplogroup definition, or they are excluded due to their instability or unreliability. Everyone else in this Haplotype Cluster is in exactly the same situation.

The only person who can see your Haplotype Cluster in Discover is you, if you are signed in to FamilyTreeDNA and you toggle “Show Private Variants” to “on.”

Haplotype Clusters as a Subset of Haplogroups

Haplogroups can and do have mutations “beneath” them, meaning haplogroup members may have different mutations or variants, in addition to the mutations used to form the haplogroup. Think of them as twigs or leaves on the tree.

Using the Classic Mitotree view in mtDNA Discover, you’ll notice that haplogroup J1c2f contains six Haplotype Clusters.

Please note that one of these clusters could be people who match the haplogroup definition exactly, and have no additional mutations of any type. They would form their own cluster.

Additionally, above the clusters, there are individual branches listed that don’t (yet) form clusters. You don’t know from looking at the individuals listed by country, such as Sweden, Germany, Norway, and so forth, if these people have only the exact mutations in haplogroup J1c2f, or if they have additional mutations that are unique and no one else has those exact mutations. What you do know is that so far, no one else matches them exactly, but as other people test, they may develop into a HaploType Cluster.

You may not match all of the people in your haplogroup on your matches page, because they may be over the match threshold and have too many mutations difference from you.

Some testers with unique, stable mutations may form new haplogroups as additional people test.

Using the Time Tree, you can see that there are currently 33 people who are in haplogroup J1c2f but do not match anyone else exactly.

The Discover Time Tree

Now that we’ve looked at examples individually, I took a screenshot of my entire haplogroup on the mtDNA Discover Time Tree to get the big picture.

The Time Tree offers a nice visual summary of all of J1c2f, including my full sequence matches, all in one place, along with Haplotype Clusters.

My haplogroup is shown in the black circle, and downstream haplogroups are shown in red circles.

You can see my Haplotype Cluster, which I can identify by the F#. You can see other Haplotype Clusters within my haplogroup, along with some individuals who don’t have any exact matches, who are shown alone on their line.

The Match Time Tree

When you click on Discover Haplogroup Reports from your dashboard, then on the Match Time Tree, you’ll see your matches’ names on your personal Time Tree, along with their self-reported earliest known matrilineal ancestors, in addition to their ancestor’s country of origin.

Here’s an example of a portion of my Match Time Tree with my matches’ names redacted.

With these new Discover and Mitotree tools, you know where to focus your research most closely. Which matches’ trees to view or build out to identify common ancestors, and who to prioritize for communications.

If you have a new haplogroup – that’s wonderful, but you don’t need one to make headway. The clue you need may well be found in your Haplotype Cluster.

There’s so much new information available for you. What can you discover?

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If you haven’t already subscribed (it’s free,) you can receive an e-mail whenever I publish by clicking the “follow” button on the main blog page, here.

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I receive a small contribution when you click on some of the links to vendors in my articles. This does NOT increase your price but helps me keep the lights on and this informational blog free for everyone. Please click on the links in the articles or to the vendors below if you are purchasing products or DNA testing.

Thank you so much.

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DNA for Native American Genealogy Webinar & Companion Book

For those who couldn’t attend RootsTech 2025, you’re in luck, because my session, DNA for Native American Genealogy, was recorded as a webinar.

RootsTech tried something new this year, and some webinars were recorded live on the actual show floor. Seating for approximately 50 people was available, but unfortunately, these sessions weren’t included in the session schedule, so no one was aware that they could attend them live.

I’m very grateful to RootsTech for making the recording widely available – and for free.

The webinar includes 10 different techniques and tools available for testers to find and confirm (or sometimes refute) Native American ancestors.

I discuss ethnicity and why it may or may not be helpful, and how to morph your ethnicity results into a tool to identify which ancestors were Native. You may have Native ancestry, even if your ethnicity results don’t reveal that. Learn how to guage that possibility and what to do next.

Y-DNA and mitochondrial DNA, yours and other peoples, can confirm or refute Native heritage in each individual ancestral line.

After we discuss each of these techniques and how to use them, we talk about creating a DNA testing plan, and various ways to find autosomal, Y-DNA, and mitochondrial DNA test candidates – or identify people who have already tested.

You can watch this webinar for free on YouTube, here.

Companion Book

I’ve also written a companion book, DNA for Native American Genealogy, which is available here for buyers inside the US, and purchasers outside the US can order at Amazon, here.

Enjoy both the webinar and the book!

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Share the Love!

You’re always welcome to forward articles or links to friends and share on social media.

If you haven’t already subscribed (it’s free,) you can receive an e-mail whenever I publish by clicking the “follow” button on the main blog page, here.

You Can Help Keep This Blog Free

I receive a small contribution when you click on some of the links to vendors in my articles. This does NOT increase your price but helps me keep the lights on and this informational blog free for everyone. Please click on the links in the articles or to the vendors below if you are purchasing products or DNA testing.

Thank you so much.

DNA Purchases and Free Uploads

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The Chauvet Cave: Trip Back in Time With Prehistoric European Humans – Are We Related?

One of the reasons I love both mitochondrial and Y-DNA testing is because it doesn’t mix with the DNA of the other parent like autosomal DNA does. This means that in additional to being useful genealogically, it provides a direct laser-line back in time – even thousands of years – to your earlier ancestors.

You’ll never know their names, of course, but you can track where they lived and where they migrated – through their mutations – breadcrumbs that function as signposts pointing the way to your ancestors. Using Discover, you can discover (pardon the pun):

  • Their migration path
  • When haplogroup defining mutations occurred
  • Other countries where ancestors of people with that haplogroup lived in a genealogical timeframe
  • Where that haplogroup is found further back in time through Ancient Connections

Your haplogroup and DNA matching is a gift from and a ticket to our ancestors that every genealogist should unwrap.

My mitochondrial DNA haplogroup is J1c2f, but the earliest tests that I took two decades ago when this industry was young positioned my haplogroup first as J, then as J1, then as J1c.

It wasn’t until a dozen years later than my full haplogroup, J1c2f was identified when the mitochondrial haplotree was initially published, then developed as more testers tested, both academically and personally at FamilyTreeDNA. Today, of course, we have the new Mitotree with even more refinement.

The earliest tests only covered the HVR1 or HVR1 plus HVR2 regions of mitochondrial DNA, while the current mtFull test covers all 16,569 locations.

Nevertheless, knowing that I was a member of haplogroup J told me something about my early ancestry, as well as provided matching to other testers. That “something” was information I could obtain no other way

In 2003, we knew that early humans had been in Europe by 50,000 years ago, Hunter-gatherers who spent their lives seeking shelter and food. We knew little else about their lives or cultures.

In 1994, stunning rock art had been discovered in Chauvet Cave in France. Thanks to a landslide blocking the entrance some 21,000 years ago, this cave and its art had been protected from humans, wildlife and the elements.

After its accidental discovery, the French government guarded and protected this astounding record of humanity with fervor, not repeating earlier mistakes in other locations, such as the Lascaux Cave, by allowing tourism which essentially destroyed those caves and their art.

By JYB Devot – Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=64503410

Chauvet cave is sealed behind a steel door with very limited access

Research at Chauvet remains closely controlled. Scientists have revealed that the stunning cave art created by early humans was older than initially thought, having been created beginning about 35,000 years ago and extending over thousands of years.

This charcoal drawing of an Irish elk was tested at location GifA 96063 (green dot) and was dated to 36,000 years ago (14C AMS). Furthermore, it’s drawn over what may be the earliest potential known depiction of an erupting volcano.

Just imagine what our predecessors must have thought when volcanos erupted.

Were the Chauvet artists Neanderthal or modern humans, or a mixture of both? We don’t know, but we do know that the earliest DNA recovered from Germany and Czechia, who surprisingly, were distantly related groups, dated from 42,000 and 49,000 years ago. They carried mitochondrial haplogroups N and R and those people were admixed and had Neanderthal ancestors. Then again, so do contemporary Europeans and their descendants.

Later papers expanded on haplogroup migration to and through Europe. We are still learning today – in many cases due to paleoanthropology or archaeogenetics by genetic anthropologists. Excavation and testing of ancient remains continues to reveal fragments and details of our human migration story.

However, back in 2003, when my first results arrived, all we knew was that haplogroup J was a European haplogroup, probably having initially formed in the Levant or Fertile Crescent – and making its way to Europe over thousands of years.

By Communication Grotte Chauvet 2 – Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=137822676

We also knew that Chauvet Cave was the earliest evidence of humankind in a specific European location – so it made sense to wonder if my ancestors were among the cave-painters.

I voraciously read everything I could find about Chauvet Cave, looking at each image and wondering if my ancestor, someplace between 1200 and 1700 generations ago, stood holding red ochre, painted those amazing spiritual images and signed their work with a handprint signature by spitting red pigment over their hand, leaving an outline on the rock wall. Was this a shamanistic ritual, connecting the shaman with the rocks with the animals they painted?

Did the practitioners perhaps hold handfuls of red ochre paint, then splat them against the wall, creating large red polka-dots that remain some 30,000 years later? Was this something fun, adding a little levity to cave painting, or maybe it depicted a wound?

Scientists tell us today that two individuals created those dots. A male that stood about 5’9” and either a female or younger male who pressed their ochre-reddened hands into the cave walls. Did they laugh as they were making art, or was this a spiritual ritual and deadly serious? Did they have a concept of “art” as we do today, or was this their form of religion? Were they praying for a good hunt, or perhaps begging for protection – or maybe both. Maybe looking to appease the Gods if the volcano was threatening to erupt.

Was a trip to the Chauvet Cave a vision quest? Perhaps a rite of passage? Were the animals either signatures of a sort, or visions?

What did they call this cave? Did it have a name? Did they have names?

I could close my eyes and see them. Were these artists specially trained in these techniques – the best of the best in their cultural group? Was it talent or training, or both? Rites of passage? There seems to be a pattern of quality among the paintings that suggest that cave painting wasn’t just left to anyone.

Was this skill or trade passed down through the generations? Was it a right of the leaders or powerful – or maybe followed specific lines? Perhaps direct maternal or direct paternal, or some other inheritance pattern?

Did the painters ritually prepare the wood, making it into charcoal used to draw the lions?

Lions? In Europe?

And rhinoceroses? In present-day France?

How things have changed!

Perhaps they used early handmade tools to engrave and scratch images into the walls for us to marvel at today. They used horsehair brushes with pigments found in their environment to paint and shape the images.

Were the horses domesticated in any way, or were they wild horses?

Did they hunt the animals portrayed – animals long extinct before modern history? Horses, aurochs, deer and mammoths? Was this their way of blessing the hunt, as such?

Many paintings depicted predatory animals such as lions, panthers, leopards, bears, buffaloes, hyenas and even rhinoceroses and are not found in any other European caves.

This hyena and leopard, which is much smaller, both have red ochre spots.

Was this art meant to absorb the power of these powerful awe-inspiring animals, or perhaps they were drawm for protection?

Or, was the act of drawing itself a rite of passage?

Why are no smaller animals portrayed? Was this a cave of special power, or powers?

The cave was inhabited during two historical periods, the first some 30,000-40,000 years ago, and the second roughly 25,000-27,000 years ago. The artwork is from the first habitation.

What happened to those people? Did they move on and cease to inhabit this region?

The remnants of hearths are found in the cave’s soft clay floor, along with a child’s footprints. So are pawprints of cave bears who hibernated there, along with their skulls and the skull of a horned ibex.

Pawprints from about 26,000 years ago are either those of a dog or wolf. Was there a difference then? Had wolves yet been domesticated into dogs as we know them?

Were the paintings meant to protect the painters and their clan? Were they shamanic portals to a spiritual world?

Did they pray to these animals as deities? Why are no humans depicted?

Who were these people?

By JYB Devot – Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=64503433

Why did they select the Chauvet Cave, high on this limestone wall, in a cliff over hung by the massive rock column known as the Pillar of Abraham, as opposed to another location? Is there a special significance? Is the location above the natural bridge relevant? Was it a meeting place or a journey destination? Did the landscape look, from a particular angle, like a prehistoric animal or deity? Some suggest the bridge bears some resemblance to a mammoth from the cave entrance.

There’s only one problem with that theory. The river elevation at that time was much higher than it is today, and the bridge wasn’t carved by the river when the caves were being painted. Many caves in the area are archaeologically significant – but nothing like the Chauvet Cave.

Why this cave?

And why did they choose the deepest recesses of the cave, nearly impossible to reach, in which to paint the best of their stunningly realistic artworks? Was the difficult journey to the cave part of the ritual itself? Did they work in a trance, perhaps? Trances and shamanic practitioners, functioning in the realm of the supernatural, are as old as humanity itself.

Did the artists join their ancestors there? Carbon dioxide levels in the cave reach levels considered unsafe in the winter months.

Were my ancestors among the hundreds of generations of those artists? Were they buried there? Did they become one with the art, the spirits, and ascend to the spirit world from Chauvet Cave?

Or, were some perhaps born in the safety of the deep recesses of the cave where the most spectacular art is found in the Gallery of Lions? Future shamans, perhaps, under the watchful eyes of the spirit animals and those shamans who had come and gone on before?

Could their power or presence be summoned?

So, so many questions.

Yes, I allowed myself to be drawn into the mesmerizing, elusive and unknowable history of Chauvet Cave.

There’s a very real possibility that my ancestors had been there.

Stood there.

Maybe participated in rituals there.

Placed red ochre on the walls.

This slide from a very early DNA presentation pretty much says it all.

I never forgot Chauvet Cave.

I also never thought I would accidentally visit.

Perhaps they summoned me.

But first, let’s go back to 1994 in the Ardèche Valley, high above the Ardèche Gorge and the natural bridge carved into the limestone by the Ardèche River millennia ago.

1994

It was a cold afternoon on a day that would live forever, shaping and changing our understanding of human prehistory. On December 18, 1994, three friends, amateur cavers, officially discovered the cave. Another person, Michel Rosa, nicknamed Baba, had discovered a hole the previous summer, which he deemed an airhole or vent into a cave, but was blocked by a stalactite that he could not get past. He was not among the group of three who would make their way into the cave that winter.

By Thilo Parg – Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=97312442

The entrance, marked above, was steep and difficult. The cave was long, and the depths, where the most remarkable art awaited, would not be reached for another several months.

Credit for discovery of the cave, and how much credit is deserved by whom is hotly disputed yet today.

Regardless, Eliette Brunel was the first to wedge her way into the hole, dropping into a world that time had frozen. After her eyes had adjusted and she looked past the crystalline deposits that had formed since the last humans visited more than 20,000 years earlier, she spotted fuzzy red lines on the wall, and exclaimed, “They have been here!”

The cave consists of six chambers, filled with prehistoric animals, plus two vulva-type figures, and perhaps one minotaur, depending on your interpretation.

These early artists achieved a realism not before known, nor discovered since, by incorporating the natural fissured and curves of the cave wall into the paintings, giving them motion, movement and life. That speaks of talent, not just copying and repeating a pattern.

Another of the three explorers, Jean-Marie Chauvet, for whom the cave was named the Chauvet-Pont d’Arc, remarked at the “remarkable realism” and “aesthetic mastery” of the early artists and their drawings.

The sophistication of these paintings exceeded that of any early works, and most later ones as well. In one word, they are unique, and we may never fully understand their genesis, purpose or impact.

Less than a decade later, when my haplogroup J DNA results arrived, the thrill of the Chauvet Cave discovery was still fresh – as was my palpable excitement about understanding the path of haplogroup J, then nicknamed Jasmine, as she trekked across Europe.

Was Jasmine in the Chauvet Cave? I don’t know.

Were my other ancestors in the Chauvet Cave? Probably, if the people of Chauvet survived? When Europe was first populated, animals and hazards far outnumbered small bands of people. A tiny village or family group of, say, maybe 20 people could easily be wiped out. Their genetic line forever extinguished.

Let’s hope that we continue to find ancient remains in Europe, and perhaps in the limestone caves along the Ardèche River. If people returned to this same location for around 20,000 years, one might surmise that the legend or custom of cave painting was passed from generation to generation, or maybe group to group. However, the truly masterful paintings seemed to only occur when the first group of people lived there.

Of course, they couldn’t return to this cave after the rockslide sealed the entrance. I can only imagine how the people, who may have been returning for time immemorial, 700-900 generations, felt to return and see their sacred cave permanently sealed.

Did they feel it was divine intervention? How did they interpret that? It seems like they would have done more than just shrug.

Did they have any concept of the number of future generations that might succeed them, as they had succeeded their ancestors for those 800 or so generations?

Probably not, but yet there I was, at Chauvet, in the summer of 2023, quite my accident.

The Surprise Visit

I journeyed to France in the summer of 2023 to travel to various ancestral locations via riverboat along the Rhone River, and to bask in the land of countless ancestors.

The tour operators offered day trips that guests could select from, and I chose one that included a walk in the beautiful village of Viviers, a visit to a lavender distillery, and the Ardèche Gorge. Truthfully, it was the lavender distillery, Maison de la Lavande, and the medieval village that hooked me. The Gorge was an added benefit.

Little did I realize…

We set out to visit the Massif Central and the Ardèche region. Ironically, I almost didn’t go, because I was concerned about the twisty curvy roads, and I didn’t want to feel ill. I sat near the front of the tour bus, just behind the driver, which afforded a wonderful view. Albeit, sometimes, a frightening view as the magnitude of the driving challenge was evident.

What I didn’t anticipate was a day trip that would include the Chauvet Cave.

The bus route through the Massif Central followed the Ardèche Gorge and winding Ardèche River, hundreds of feet below.

The river carves its way through the limestone cliffs, sculpting the land beneath and beside it’s wandering path.

It’s truly a long way down. Kayakers enjoy the slow-moving waters.

Kayak rentals abound along the lower reaches of the river.

The road runs high in the mountains, parallel to the river gorge, with overlooks at a few locations along the way. Few places have enough space for an extra lane, so overlooks are quite limited.

It was difficult for me to fend off motion sickness, but I managed, and it turned out to be well worth the effort.

It was an exceptionally hot day, so excuse my appearance.

If I look happy here, I didn’t yet know that the Chauvet Cave would present itself, literally, in front of me.

I hadn’t thought about the Chauvet Cave in some time and hadn’t put two and two together.

A few hours into our journey, we needed to stop for a bathroom break, to give the poor bus and driver a break, and to eat lunch.

When you are driving along the road beneath Chauvet Cave, at the base of the cliffs, you can’t see much of anything except foliage.

You can see the little walk in the field that begins a very steep hike and climb onto the cliffs. I took pictures here with absolutely no idea what I was photographing, although this one is from Google Maps later. What were the chances of taking a photo of that exact place and discovering it only later after the cave’s location had been pointed out to me?

The cave is unmarked, so you’d never know it was there if you didn’t know. We drove right past this incredible site, and no one was aware. It hadn’t clicked yet for me, either.

This unremarkable, humble little fence is the only clue. If you’re worried about me revealing the location, don’t be. The site is impenetrable.

You can see the loop, the location of the cave, the “person” on the road beside the stone building where we ate, and the camera icon is the natural bridge.

Our lunch stop, the stone building above, is essentially the only place in the area that has amenities with parking that could accommodate the bus. There were no other choices, but it was lovely and we didn’t care. I’ve marked the cave to the right, but we still had no idea.

When I say amenities, I mean remote French country, with a very cute, rather rustic but very clean building surrounded by flowers.

We piled out, stood in line for the restroom facilities which had been built onto a historic stone building without restroom facilities. There are very few new buildings in France. You can tell this is the only facility for many miles because this sign expressed exactly how we all felt.

We had a good laugh.

We were invited to find a seat at the few tables at what I think was actually a campground. There were maybe three tables inside and several more outside on the patio.

I’m an outside person, hot weather or not, so I found my way to the most distant table, beneath a tree, across from the vineyard, beside a flower box. Yes indeed, this is my idea of a wonderful, peaceful respite.

I could stay here forever.

This choice would turn out to be an incredible “happy accident.”

One of the two servers brought us a pitcher of ice water and glasses. And wine. Every meal has wine, but I’m not a wine connoisseur so my husband always gets mine too. I’m happy and he’s very happy:)

When traveling as a group, you often don’t get a lunch choice, or if you do, it’s either item 1 or item 2. I don’t recall what I selected. The menu was in French and I got the gist of it, but it really didn’t matter – I’m flexible and like to try new things. Often Jim and I order something different so we can both try two new things. We call it “adventure eating.”

Keep in mind that France is a much more laid back place than the US. Lunch may take an hour. Maybe two. Maybe all afternoon. It’s more about the event and the camaraderie and enjoying the food that getting full.

As we relaxed, waited for our lunch, enjoyed the wine, and chatted among ourselves, for some reason, it struck me that I thought I recalled that the Chauvet Cave was someplace in this region.

I had no cell reception, so I found our lovely French tour guide who was sitting inside with our bus driver, and asked.

I struggle with French, and she struggled with English, so I thought sure she had misunderstood my question when her answer was “Oui, Juste ici,” meaning “Yes, right here.”

No, I didn’t mean generally – I mean where, exactly? Will be pass anyplace close?

Yes, she replied, “it’s right here.”

Wait? What?

Me: Chauvet Cave?

Her: Oui, Grotte Chauvet?

Me: Where?

Her, pointing: “Juste là-bas.“ – Right over there.

Me: Vraiment? (Really?)

Her: “Oui, vraiment.”

My incredulity must have been written all over my face.

She came outside and sat down beside me. I showed her my phone with a picture of a map from earlier. She put the phone on the table and started pointing.

I was very confused.

She stood up and motioned for me to come with her.

We walked across the gravel road to the vineyard and she began to point.

“Right there,” she said, “on the cliff.”

“Where on the cliff?”

“Under the bushes?”

“Which bushes?”

I took this picture, and she pointed to the bushes beneath the rocky portion of the mountain, to the right of the large bushy glob, for lack of another word.

I was utterly and completely dumbstruck.

Speechless.

I stood mute in disbelief.

I finally found my words again and asked how she knew the exact location of the cave? She told me she lived in the little nearby village, and her friend actually discovered the cave. Everyone, she said, who lives there knows exactly where it is.

How is this even remotely possible?

July 8, 2023 – Facebook posting

OMG, I’ve died and gone to Heaven. I’m literally at the Chauvet Cave, the oldest evidence of human art in Europe. And it’s beyond stunning.

I’m pinching myself.

I had no idea we’d be here. This is not a bucket list item for most people, but it assuredly is for me. I’ve worked with and studied human migration for 25 years now, and this cave is sacred.

Very few people inhabited what would be Europe 35K years ago. Those that did painted this cave, recording animals we had no idea lived here. They were probably the ancestors, one way or the other, of most Europeans and their descendants today.

As luck would have it, a friend of our guide that lives in her tiny village discovered the cave, so she knew exactly where it is – and showed me.

Better yet, I’m having lunch looking directly at the cave. I feel like I’m living a dream. First this stunning location and then to discover I sat myself in front of the cave.

I truly could not believe the incredible odds that I would accidentally manage, by happenstance, to wind up having lunch is a remote region of mountainous France, literally looking at Chauvet Cave immediately in front of me.

And, by luck of the draw, have a women from this area who knew exactly where the cave is as my tour guide – for a tour that originated maybe three hours away on the Rhone River.

Tell me my ancestors weren’t calling to me.

I sat spellbound, eating the artistic, beautiful food, in the best seat in all of the Ardèche Department in France.

I cannot take my eyes off of the limestone cliff wall – connecting with those people who walked there, perhaps my most distant ancestors in Europe, across 40,000 years. I wonder how those humans originally found the cave. Were they seeking shelter?

We had some free time, and I left the group and walked alone in the vineyard that stands as a silent sentry today. Did the people who painted the cave also cultivate any agriculture, or was that still too early in human history.

I was spellbound to this place and that time. Utterly transfixed.

I saw a path, and I had to explore. Isn’t that the story of my life. Is that what they did, too?

I walked towards the cave, which seems to beckon me. Perhaps the cave that sheltered humanity, allowing us to survive.

I feel like I’ve been drawn home to the cradle of European humanity – the wellspring of our shared human story. Hooked like an unwitting fish in the water and reeled right in by some powerful ancestral force.

I don’t know how to describe this surreal moment other than perhaps some combination of an out-of-body experience and transcendent state of flow. Time paused, or perhaps collapsed in on itself. The boundaries between then and now, and them and me, dissolved. It felt both ancient and present – beyond time as we understand it – an umbilical cord somehow inexplicably tethering us.

Words are entirely inadequate.

In this picture, you can see the steep access path, beneath the rocky ledge, and other caves as well.

You’ll notice other limestone caves all along the cliffs throughout the region, but none of those caves even hold a candle to Chauvet – and none were treated in the same way. Why was Chauvet special?

Caves aren’t easy to access. Either they are high on the cliff walls, requiring either rappelling down or climbing up through narrow paths, then fissured rocks.

Here’s a nearby limestone cave. And no, I did not go splunking. Being with a tour group does not afford that amount of flexibility – especially since the cave wasn’t even on the agenda at all. Plus, by this time, I was alone, and you NEVER embark on a risky adventure alone. I’ve been there, done that, and broke my ankle in the process. Plus, there was more to see.

I turned around and hiked down to the river to see what awaited there.

This area is extremely popular with kayakers who walk their kayaks down this path and launch just before the beautiful natural arch bridge which you can see, at left, above.

By Jan Hager – Own work, CC BY-SA 4.0, https://commons.wikimedia.org/w/index.php?curid=51738871

After reaching the water, I decided to hike on the path above and along the river, which afforded me a stunning view of the river, bridge and the mountains on both sides.

I suddenly realized that the river level 35,000 years ago was MUCH higher than it is today. It didn’t run beneath the arch, which hadn’t yet been hollowed out, but over the top, which meant the valley floor was also elevated.

OH!

The river is to my immediate right, and path in front of me continues straight to the mountains, or turns left to Chauvet. Isn’t that the perfect metaphor for life.

Standing at the intersection of the walk to the river, and the path alongside the river, you can see the bridge in the center, just to the right of the fence, the mountains on both sides, and Chauvet to the far left.

On this photo, I’ve marked both the top of the arch of the bridge, and the Chauvet cave, with red arrows. Based on the elevation, you can see that before the river carved the bridge, the landscape of the valley would not have been worn away, and human access to the cave would have been much different. In other words, the valley floor would have been much closer to the cave.

This makes so much sense.

As much as I wanted to stay, it was time for me to go.

I found it ironic that on the way back to join the group at the bus, I found this sign which, translated by ChatGPT, says:

The Invisible History of the Pont d’Arc

The arch of the Pont d’Arc is a unique natural monument in the world.
It has probably fascinated humanity for millennia.

Like a totem, it evokes a gateway between two worlds: the visible and the invisible, the familiar and the wild, mystery and knowledge.

Hidden within this setting is the decorated Chauvet-Pont d’Arc Cave,
classified as a UNESCO World Heritage Site.

It has revealed to our amazed eyes drawings over 36,000 years old.

But did you know that this site holds other hidden stories?

By exploring the Combe d’Arc, discover the invisible stories sheltered by this majestic landscape:

    • how water sculpted, drop by drop, this mineral arch
    • how, over the ages, humans found their place in this extraordinary location

Introspective Journey

While the rest of our tour group had lunch, sandwiched between two other stops, plus some time to walk along the river and view the natural bridge, I had taken an amazing journey back in time and visited ancient humanity. The people who painted those incredible images in the Chauvet Cave are probably the ancestors of every European, assuming even one of them survived to reproduce, or the ancestors of no one today, if their lines perished.

One way or another, humanity did survive, and standing on this sacred site allows us, today, to glimpse a time far in the past – just as our mitochondrial and Y-DNA do as well.

Our own ancestors speak to us from long ago, and the mutations we carry from them light the way back in time, through the Ardeche and the mountainous regions of France, expanding into the rest of Europe.

A priceless window in time.

Indeed, as Eliette exclaimed, “They have been here,” and perhaps they still are, in us.

Resources

If you’re interested, I found three YouTube videos that expand upon the Chauvet Cave.

My one regret is that I didn’t know about the Cavern du Pont-d’Arc, a vast to-scale reproduction of the Chauvet Cave. I would have found a way to visit, even if I had to hire a private driver for a day.

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New “Share” Features at FamilyTreeDNA Blur Match Information and Make Sharing Easy

Have you ever wished you didn’t have to blur or otherwise redact each name and other sensitive information in order to share your DNA match results? Or maybe you’d like to share fun Discover pages? Well, you got your wish!

FamilyTreeDNA has introduced a new “Share” feature in two locations. The first Share feature is available in your personal account after signing in, and two additional features can be found in Discover.

  1. “Share Mode” on your personal page obfuscates the names and photos of your matches.
  2. “Share Mode” in Discover obfuscates the names and photos of your matches on your Match Time Tree.
  3. “Share Page” in Discover shares publicly available pages to social media or provides a sharing link for you.

These are extremely easy to use and help immensely, allowing you to share screenshots on social media and with family without revealing the names of your matches.

I’ll show you, step-by-step, how to use all three.

“Share Mode” in Your Personal Account

When you want to enable Share Mode, you just toggle it on.

Sign in to your account at FamilyTreeDNA.

Select Account Settings beneath your name in the upper right-hand corner.

Under Privacy and Sharing, toggle Share Mode to “ON.” Default is “OFF.”

Sharing turns itself back off each time you sign out, so you’ll need to do this each time you sign on and want to share.

To see the results, let’s take a look at my match page. Sharing works the same way for Y-DNA matching, mitochondrial or Family Finder.

Not only does Share obfuscate your matches’ names, it also blurs their picture, and your information as well, at upper right.

This is wonderful for presenters!

Using “Share Mode” in Discover

On your dashboard, for either Y-DNA or mitochondrial DNA, select “Discover Haplogroup Reports” in the appropriate section.

Discover has two ways to share.

You can share your Match Time Tree, or other pages – using different tools.

Only one Discover page, the Match Time Tree, contains potentially sensitive match information. There’s a “Share Mode” for the Match Time Tree that blurs private information.

However, you may want to share your other Discover reports on social media. “Share Page” provides a quick and easy way to share any publicly available page.

Let’s look at both of those options.

Discover “Share Page”

Every page in Discover, except for the Match Time Tree and Globetrekker, has a “Share Page” icon at the top.

You can share any Discover page on social media (except as noted below), whether you’ve clicked through to Discover from your dashboard, or you’re using the public version of Discover.

In this case, I clicked on “Share Page” to share my Haplogroup Story page to Facebook. On your social media platform of choice, or by sharing the link, your friends can click through to see the page you’ve shared – minus your name and photo.

Please note that there are four Discover pages that either do not share or will display reduced information when using “Share Page,” as follows:

  • Globetrekker is an amazing animated video of your ancestors’ trek across the planet which is reserved for FamilyTreeDNA clients who purchase the Big-Y test or the mtFull, full sequence mitochondrial DNA test. Globetrekker does not use the “Share Page” feature, and is not yet released for mtDNA Discover.
  • Ancient Connections uses the “Share Page” feature, but only publicly displays a few ancient DNA haplogroup matches. Several more are reserved for testers who have taken either the Big-Y or mitochondrial DNA full sequence test, and click through from their dashboard. In a kit I just checked, two or three displayed when shared publicly, but the tester had more than 20 when clicking through his dashboard.
  • Notable Connections uses the “Share Page” feature and functions like Ancient Connections.
  • The Match Time Tree does not use the “Share Page” feature, which populates to social media, but there is a “Share Mode” option which blurs your matches’ sensitive information, similar to your personal page. After blurring, you can take screen shots to share.

Discover Share Mode for the Match Time Tree

The Match Time Tree on Discover is an extension of matching – meaning that your matches are placed on the Time Tree with names of tester-provided Earliest Known Ancestors (EKA) and their country of origin listed.

To view your Match Time Tree, click through to Discover from your FamilyTreeDNA dashboard, then select “Match Time Tree.”

You need to enable “Share Mode” within Discover, even if you had it enabled on your personal page. Toggle “Share Mode” to ON at the top of your Match Time Tree page.

Enabling “Share Mode” obfuscates the names and photos of people on your match list, who now appear on your Discover Time Tree in their proper place. You’re there too!

To share this page publicly, you’ll need to take a screenshot – so please don’t forget to enable “Share Mode” within Discover before doing this.

Benefits of Sharing

The best thing we can do for DNA testing, speaking broadly, is to encourage additional testers who are excited about what they can discover.

Sharing our pages and discoveries on social media is a great way to generate excitement.

Who do you know that might be excited to discover that they share an ancestor with Leo Tolstoy or maybe “Wild Bill” Hickock, even if it’s hundreds of years ago?

How about discovering that an Ancient Connection is a Viking man who was buried in Shestovista, Ukraine about a thousand years ago, and you two shared an ancestor about 1900 years ago? Might that provide a clue about your genealogy? What was the life of your ancestor like?

Or, maybe your friends and relatives would be excited to view the path their ancestors took, marching across the map, until their ancestor arrives on the globe where their haplogroup is most recently anchored?

Trying to get Uncle John or Aunt Mary to test? What kind of information would they think is cool?

A scientist I know especially loves the Ancient Connections that extend far beyond the reach of surnames.

One of my ancestral lines has an ancient DNA match just 9 kilometers from the town where they are rumored to have originated in France. Along the ancient Roman road. How else would I have EVER made this discovery?

The more people that test, the larger the matching pool – and the better for all genealogists.

Thank you to FamilyTreeDNA for introducing “Share Mode,” which makes sharing matches with other researchers effortless, and for “Share Page” within Discover, which makes sharing publicly a breeze!

Who can you share and collaborate with?

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Here’s the link. Just look for the black “follow” button on the right-hand side on your computer screen below the black title bar, enter your e-mail address, and you’re good to go!

In case you were wondering, I never have nor ever will share or use your e-mail outside of the intended purpose.

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Share the Love!

You’re always welcome to forward articles or links to friends and share on social media.

If you haven’t already subscribed (it’s free,) you can receive an e-mail whenever I publish by clicking the “follow” button on the main blog page, here.

You Can Help Keep This Blog Free

I receive a small contribution when you click on some of the links to vendors in my articles. This does NOT increase your price but helps me keep the lights on and this informational blog free for everyone. Please click on the links in the articles or to the vendors below if you are purchasing products or DNA testing.

Thank you so much.

DNA Purchases and Free Uploads

Genealogy Products and Services

My Books

Genealogy Books

Genealogy Research