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each donor arrives, they wait to be checked in. This, we jointly decided, was the best time for us to<br />

introduce ourselves and to ask for their consent to having us analyse their DNA. I was extremely<br />

fortunate in having a team of researchers in my group at the time who were absolutely brilliant in<br />

the art of persuasion. To the waiting donors, we explained that we were creating a new genetic map<br />

of Britain and trying to work out from it our Celtic, Pictish and Viking roots. That was about all the<br />

explanation anyone needed before agreeing to take part, especially when they realized we would<br />

only be taking a sample of blood from their donation, so there was no need for another needle.<br />

Donors told us where they were from, as far back as their grandparents. Those who didn’t know,<br />

generally the men, took a purple form home with them to ask someone in the family, invariably a<br />

woman, and sent it on to us.<br />

By the end of the session in Auchterarder we had collected 187 blood samples, a wonderful<br />

start. Over the next two years we visited almost all of the donor sessions throughout Scotland, from<br />

Galashiels and Thornhill in the Borders, to Thurso at the very top of Caithness, to Stornoway in the<br />

Western Isles, to Campbeltown on the tip of the Kintyre peninsula. Everyone in my research lab<br />

joined in, even if they were working on different projects. Itineraries were prepared so that, with<br />

luck, several different sessions in different regions could be covered in one trip. We travelled to<br />

Scotland by road, by air or by the Highland sleeper from Euston. We set aside a small office at the<br />

Institute as a planning room, with donor-session schedules on the wall and a large map of Scotland<br />

next to them. By the time we went to our last Scottish session, two years later in Fort William, we<br />

had collected over 5,000 blood samples and clocked up over 50,000 miles between us. It is a<br />

testament to the team’s powers of persuasion that we only ever had one person decline to take part<br />

in the project – a farmer from Callander in the Trossachs, north of Stirling – who had to rush off<br />

because one of his cows was about to give birth and he didn’t have time to fill in our form. It says a<br />

lot about him, and donors in general, that they take their blood donations very seriously. None of<br />

the donors is paid a penny and the sessions have a tangible atmosphere of selfless community<br />

service. Most sessions are entirely run by women, with the only men present being the drivers of<br />

the vans that bring the teams and the equipment. It was friendly, calm and efficient. Very impressive<br />

all round.<br />

To begin looking for the genetic signatures of the Picts on the mainland I began by dividing<br />

Scotland into regions. It was easy to decide where to draw the line on Orkney, Shetland and the<br />

Hebrides – they were islands – but on the mainland I needed to draw boundaries. These are shown<br />

on the map on page 15. Pictland was covered by two of these: the Grampian region and Tayside<br />

and Fife, which for convenience we will henceforth refer to simply as Tayside.<br />

Since we began our analysis of the Northern Isles with the Y-chromosome, and also in<br />

deference to the Pictish tradition of matrilineal inheritance, we began the search with<br />

mitochondrial DNA. The clan proportions for both Pictish regions were remarkably similar to one<br />

another – again you can see this in the Appendix. When I put the results through a statistical test, the<br />

only clans that had a significantly different frequency in the two regions were Jasmine, higher in<br />

Grampian, lower in Tayside, and Tara, higher in Tayside, lower in Grampian. Otherwise there was<br />

no difference. It looked, at this level of scrutiny, as if the maternal ancestry of the two Pictish<br />

regions was almost indistinguishable one from the other.<br />

When it came to analysing the detailed sequences, though, I could see plenty of differences.<br />

That is always to be expected, because a large proportion of mitochondrial sequences are unique to

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