Many members of the Calhoun family have participated in genealogical genetic testing, particularly Y-DNA testing. This is the first of two posts that I wanted to devote to what we have learned from these results so far. Most people participate in genealogical genetic testing because they want to learn something about their own personal ancestry. However, the crowd-sourced nature of comparative genetics means that everyone’s individual results also tell us something about testers as a population, in this case the Calhoun family. The conclusions I draw here can and probably will change as more family members participate and we develop an ever clearer picture of the family’s structure. Although we have learned a lot already, I would encourage all Calhoun family members to join in this effort, whether you know a lot about your own ancestry or not.
Y-DNA Genetic Testing
Modern genealogists and family historians have two parallel tracks of evidence available to them. One is a paper trail of historical documents, often supplemented with oral history and tradition, stating personal relationships between people. The other is genetic testing results, which provide evidence of biological relationships between people. These two tracks provide complementary information, and each can sometimes help to overcome roadblocks in the other.
There are several types of genealogical genetic testing, but Y-DNA testing, which looks only at the Y-chromosome, is the type best suited for the study of males with a particular surname. This is because the Y-chromosome, found only in men, is passed nearly unchanged from father to son, in the same way that surnames are typically passed down in Western societies. I say “nearly” unchanged because it does undergo occasional changes (mutations), and these minor differences allow us to compare testers to one another and estimate when their most recent common patrilineal ancestor may have lived. In general, Y-DNA of men who are more closely related will have fewer differences than those of men who are more distantly related. Two kinds of mutations are commonly examined for genealogical purposes: short tandem repeats (STRs) and single nucleotide polymorphisms (SNPs). For further information on how Y-DNA testing works and what the terminology is, a good resource is the ISOGG wiki page on Y-DNA tests.
At present, the company that does the most genealogical Y-DNA testing and has the largest match database is FamilyTreeDNA (FTDNA). FTDNA offers both STR testing and comprehensive SNP testing, the latter via a relatively new test called “Big Y”. In contrast with STR mutations, which change back and forth between states relatively frequently, SNP mutations are very stable, meaning once one occurs, it is unlikely that it will later change back to its original state. This means the Big Y test provides more accurate results than STR testing alone. However, it is more difficult to perform: while STR tests only need to examine a relatively small number of predetermined locations on the Y-chromosome, comprehensive SNP tests like Big Y require a more open-ended search that interrogates hundreds of thousands of locations, not only determining the states of previously known SNPs but also looking for new ones.
Surnames and Y-DNa
The earliest heritable surnames in Britain are just under 1,000 years old. When two men whose most recent patrilineal common ancestor lived less than 1,000 years ago share the same surname, the simplest explanation is that their common ancestor had that surname, with both men inheriting it by unbroken patrilineal descent. When two men whose most recent patrilineal common ancestor lived more than 1,000 years ago share the same surname, it is not by common inheritance, and several alternative explanations are possible. Some examples:
- The surname was acquired independently by several founders in early medieval times, and each man has inherited the name from a different founder.
- At some point in the ancestry of at least one of the men, the surname was acquired from an adoptive father, not a biological one.
- At some point in the ancestry of at least one of the men, the biological father was not the mother’s husband.
- At some point in the ancestry of at least one of the men, the surname was acquired from the mother (perhaps because she was unmarried), not from the father.
In the first example above, each independently founded family with the same surname would be of comparable age, resulting in––theoretically, at least––comparable numbers of modern male-line descendants. The last three examples above are referred to in genetic genealogy as non-paternity events (NPEs), and they can occur anytime between the early medieval period when surnames were first acquired and the present day. Generally speaking, the more recent the NPE, the fewer the number of possible descendants in the present day.
The calhoun Surname project
Because Y-DNA tests are so often used to study ancestry within a surname group, FTDNA hosts client-administered research projects for many surnames. One of these is the Calhoun Surname Project, which as of this writing has 416 members, roughly 250 of whom have posted Y-DNA testing results for comparison. Of the 250 tests, roughly 100 include Big Y SNP profiling. Because Big Y is newer and more expensive than STR tests, fewer people have taken it, but the numbers are growing, and I would encourage any Calhouns who are considering testing for the first time, or who have only taken STR tests, to take or upgrade to Big Y.
The Calhoun testers fall into several Y-DNA genetic groups (haplogroups) that are for all intents and purposes unrelated to each other. (In other words, with common paternal ancestry long before the surname era.) As of this writing, the Calhoun Surname Project identifies 8 haplogroups that include more than one tester with the name Calhoun, at least one of whom has tested to 111 STR markers or more. The following table shows, for each of these 8 groups, the haplogroup name (as per the Project), the number of testers to date, and a description of the group members:
Group | Size | Members |
E1b1b1 | 107 | Calhouns, Kilpatricks, McCarters from Scotland, Ireland, America, and elsewhere. Common haplogroup of the Calhouns and McCarters BY5775 (ca. 1100 CE). |
R1b1a2_A | 12 | Mostly descendants of Samuel, son of William Cahoon (1633-1675), Scottish prisoner transported to Massachusetts. Possible haplogroup BY76688 (ca. 1550 CE). |
R1b1a2_C | 12 | Mostly descendants of William Cahoon (1633-1675), Scottish prisoner transported to Massachusetts, by various sons. No Big Y testers. |
R1b1a2_N | 5 | Calhouns with Irish roots. |
R1a1_A | 4 | Colquhoun family from Argyll, Scotland, including descendants of Archibald Colquhoun (1758-1839) and Mary McCorquodale, and Malcolm Colquhoun (1767-1823) and Christian McCorquodale. |
R1b1a2_G | 3 | Calhouns with Scottish roots. |
R1b1a2_M | 3 | Stated descendants of Patrick Calhoun Sr., grandfather of US Vice President John C. Calhoun. (Others of his descendants belong to E1b1b1.) |
J2 | 2 | Samuel Colhoun of Ireland and his son John Colhoun (1845-1916) of Trinidad and Tobago. |
Note that one of these haplogroups, E1b1b1, is more than twice as large as all of the others combined. I suggest that this haplogroup represents the Y-DNA lineage of Humphrey of Kilpatrick, 13th century founder of the Calhoun family, for several reasons:
- It includes by far the largest number of testers, suggesting it has the most descendants today and is therefore the oldest of the groups above. (However, there are alternative explanations for this.)
- The SNP common to all Calhouns in this group, BY5775, is believed to have arisen about 1100 CE, give or take a couple of centuries, which is consistent with the adoption of the Colquhoun name by Humphrey of Kilpatrick around 1240 CE.
- It includes Calhouns from many families, from Scotland, Ireland, America, and elsewhere, suggesting it predates the dispersion of the family from its Scottish homeland.
- Some of the closest genetic relatives of the Calhouns within this group have variants of the name Kilpatrick, which is consistent with a name change from Kilpatrick to Colquhoun by Humphrey.
All the other haplogroups above are much smaller, and the common ancestors of the Calhouns in each appear to be much more recent, than in E1b1b1. This suggests that all of the other seven groups above originated with breaks in the co-inheritance of Y-DNA and surname from the original lineage, i.e., NPEs.
The fact that there is only one haplogroup with both a large number of testers and common ancestry in or before the 13th century supports the idea that the Colquhoun name was adopted only once in medieval times, by a single individual. Based on the data we have now, no other Calhoun haplogroups are as old as the 15th century, which is when some Scottish commoners began adopting the surnames of their clan chiefs. In my earlier post about the origin of the Calhoun family, I stated that I saw little or no evidence of this practice within the Colquhoun clan, at least on a wide scale, and this is why. Of course there are many assumptions in this hypothesis, including “every male founder has a comparable number of patrilineal descendants”, “there is no bias in who decides to take a Y-DNA test”, etc. I recognize this, but it’s the best I can do for now, and I welcome any comments.
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Thanks to Marc McDermott for kind permission to use and modify his figure, and once again, special thanks to Paul Calhoun for critical reading of this post and helpful edits.
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© 2023 Brian Anton. All rights reserved.
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