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The Irish Origin
of the surname 'Butler'
The
surname of the Butlers of Ireland has its origins in the hereditary office of ‘Butler
of Ireland’ originating with Theobald Walter, 1st Chief Butler
of Ireland who lived in the 12th century. Theobald was granted the
hereditary title of Butler of Ireland, or ‘Pincerna Hiberniae’, having
served as butler to Prince John who was created Lord of Ireland in 1177 by his
father King Henry II. The 7th Chief Butler, James Butler, was
created 1st Earl of Ormond in 1328.
In
royal households, the title denoted a high-ranking officer and the ‘butler’ was
one of the top five ranked senior offices in the household, along with the
chamberlain, the seneschal, the chancellor and the constable. While officially
in charge of the wine cellar/buttery and all of the under-staff required in
that position, he held other important duties such as serving the king his wine
at dinner, presenting the newly crowned king his first cup of wine as monarch,
and other appointed duties required at court.
While
the family surname was ‘Walter’, Theobald’s heirs and descendants
adopted the surname ‘le botiller’ and then ‘Butler’.
The
following blog URL links, explore the history of Theobald Walter and his Norman
origins.
Theobald Walter,
Chief Butler of Ireland
Part 1: Ancestral origins of Theobald Walter, ancestor of the Butlers of
Ireland, and the history of the Walter family
Part 2: Ancestral origins of Theobald Walter:
possible candidates for the Walter surname named ‘Walter’ in the Domesday Book
Part 3: Ancestral origins of Theobald Butler:
Analysis of the various theories of the origins of the Walter family:
Part 4: Ancestral origins of Theobald Butler:
The Lands held by the Walter family:
https://theobaldwalter-1stbutler-of-ireland.blogspot.com/2022/07/part-4-ancestral-origins-of-theobald.html
Y-DNA GENEALOGICAL TESTING
The newly developing
science of genealogical Y-DNA matching will probably gain
momentum in the coming years and may play an important role in unraveling these
family tree mysteries and help with matching family links. It may also pose new
unanswerable genealogical questions as well. DNA can provide information about
our ancestor's migratory paths through thousands of years as well as individual
descent from one's forebears. The same DNA markers are handed down from
generation to generation for hundreds even thousands of years, with occasional
mutations of individual markers in the DNA profile. A recent example was the
use of DNA matching to identify the remains of King Richard III whose bones
were found in a carpark in Leicester. Also the remains of the Russian Imperial
family, murdered by the Bolshevics in 1917, were identified using Prince
Philip's DNA (through his mother) and the Y-DNA of a Russian Count living in
France. Two types of DNA testing were used in these cases- Y-DNA passed down
through the male line (from father to son) and Mitochondrial DNA (mtDNA) passed
down through the female line (although mtDNA is passed from the mother to both
male and female children, only the female child can pass it onto her
children).
The mtDNA of Richard III matched two living relatives of eldest sister Anne of
York who held a rare additional genetic variant, which carried down through the female line.
Wikipedia states: “A genealogical DNA test is a
DNA-based test which looks at specific locations of a person’s genome in order
to determine ancestral ethnicity and genealogical relationships. Results give
information about ethnic groups the test subject may be descended from, and
about other individuals that they may be related to.”
Everyone inherits 23
pairs of chromosomes, half from each parent, including 22 pairs of autosomal chromosomes and 1 pair of sex chromosomes, either XY (male)
or XX (female).
Three principal types of genealogical DNA tests are
available, with each looking at a different part of the genome. The three types
of genealogical DNA tests:
1) AUTOSOMAL TESTS look at chromosomes 1 to 22 and X. The
autosomes are inherited from both parents and all recent ancestors. The number
of markers (SNP’s) inherited from a specific ancestor decreases by about half
each generation, so this test is mainly useful to determine close relationships
(ie. up to about 4th-5th cousin level), as the amount of
DNA inherited dilutes with each generation back in time (half from each parent,
quarter from each grandparent, one eighth from each great grandparent, etc). The
test also gives one a general idea of ethnicity based on the testing company’s
databases, but these often change in time as more testing is conducted. This
test is the one offered by Ancestry.com in its advertisements, as well as FamilyTreeDNA,
23 & Me, and My Heritage. Using these large and growing databases, the tests can
also provide information about the ethnicity of one’s ancestors, which regions
of the world they likely called home, and are gaining a better understanding of
the unique genetic variations for each reference population.
2) Y-DNA TESTS look at the Y-chromosome, which is inherited father to son, and so can only be taken by males to explore their
direct paternal line. As the Y chromosome is inherited with little change for
generations, it is useful to determine and prove the paternal line for many
generations back. It also provides information on the paternal line going back
thousands of years, and one’s ancestral origins, divided into ancestral groups called Haplogroups. This test is only provided by the company FamilyTree
DNA (FTDNA).
3) mtDNA TESTS look at the mitochondria,
which is inherited from mother to child (to both male and female) but can only be passed on by the female, and so can be
used to explore one’s direct maternal line back into the distant past. It also
determines the maternal ancestral origins, or, Haplogroup. This test is
provided by FTDNA.
This blog article is only concerned with the Y-DNA
testing of a male descendant of Laurence Butler, who inherited his Y chromosome. The aim of the Y-DNA test was to provide proof of that descent, and ultimately to try and determine Laurence’s
paternal ancestry in Ireland, as well as his ancient paternal
origins/Haplogroup.
DNA is the only genealogical record that is absolute proof of one's true
heritage, and combined with the traditional genealogical paper trail, it
promises an exciting future in family research. Research estimates there is a 1-3% rate of false paternity per generation.
Y-DNA is passed down from father to son, as only the male child inherits the Y chromosome from his father. And it is through the Y-DNA tests that Surname genealogical groups can be set up such as the Butler Surname Y-DNA Project. This project aims to try and sort out the different origins of Butlers, such as the varied Butler family groupings with origins in Ireland and England, worked out by the late Lord Patrick Dunboyne, as seen on the Butler Society website.
Surnames were established in Britain about 700 years ago, and the correlation between Y chromosome type and surname is complicated by several factors. Common surnames named after occupations, such as Smith, Butler, Carpenter, Cooper, Weaver, Cook, etc., or from patronyms such as Johnson, Jackson, Williamson, Williams, etc., had been founded independently more than once and have relatively large numbers of founders. This will result in more than one Y type being associated with a given surname. Non-paternity events, the adoption of male children, the tradition of the servant classes of taking their master's name, the husband or son of a sole heiress taking her surname for inheritance purposes, and deliberate name change will have the same consequence. Genetic drift, known as 'daughtering out', can lead to the extinction of some Y chromosome lineages, and is responsible for the complete extinction of some British surnames, and consequently can lead to the increase in the frequency of other lineages within the surname groups.
At this point, the Butler Surname Project bears this out, as there is no single lineage standing out as predominant in the Y-DNA results, and subsequently there are a large number of unrelated Butler lineages showing up.
It should also be remembered that, at ten generations back, an individual has up to 1024 unique ancestors, and a Y-DNA test is only studying one of those ancestors.
DNA also determines our deep ancestry, viz. from where our ancient ancestors originated. The ancient migratory paths of ancestors out of Africa, tens of thousands of years ago, have been grouped into HAPLO groups.
HAPLOGROUPS
All the world's peoples are divided into ancestral groups called 'haplogoups', using their DNA code.
A Haplogroup
is defined as a genetic population group
of people, or, a group of
similar haplotypes that share a common ancestor on the patrilineal or
matrilineal line;
and a haplotype
is defined as a group of genes or a set of DNA variations which is inherited
together by a single parent.
It is like a pedigree chart of the different clans of humans throughout the world.
The earliest haplogroups were found in Africa. As people moved away from Africa and crossed into Asia and Europe and then spread further into the Americas, Australasia, etc, they developed unique mutations in their genetic code that would give rise to the various human clans worldwide, dating back tens of thousands of years ago. A new haplogroup is formed when a specific new mutation occurs in a chromosome of an individual, and all descendants carry that mutation.
The different haplogroups worldwide have been assigned a letter
of the alphabet, and refinements consist of additional number and letter
combinations eg. Haplogroup 'R' can be divided into R1a and R1b, and further
R1b1b1a…; and Haplogroup 'I' can be divided into I1 and I2 etc.
With each mutation, called a Single Nucleotide Polymorphism, or 'SNP' for short, a subgroup or subclade of the original haplogroup begins a new haplogroup. As more and more haplogroups are rapidly being discovered as more SNP's downstream are discovered, the old letter numbering system is becoming unwieldly and will probably change, and may give way to the label of the lowest branch, or terminal SNP, to identify one's haplogroup, eg. Haplogroup 'I- L813' means original haplogroup 'I' (originating in northern Europe around 25,000 years ago) and subclade terminal SNP 'L813' which indicates a single ancestor with a unique mutation living about 1700 years ago in Norway. This subclade will be further refined as more SNP's are discovered 'downstream' of L813, and the time-frame of the most recent ancient ancestor is reduced further, giving rise to a new terminal SNP.
To understand these different groupings, one would need to read
some of the numerous online articles on this subject. Suffice to say that the
most common Haplogroups for western European ancestry fall into the Haplogroups I and R and their subclades.
Haplogroup I (I1 and I 2) is of 100% European origin and represents nearly one-fifth of the European
population, whereas the R1b haplogroup which
represents the majority of Western Europeans, is Eurasian/Indo-European and believed to have originated
in West Asia/India.
Estimates
of the age of Haplogroup I suggests it arose prior to the last Glacial
Maximum (approx. 25,000 years ago), and is the oldest Haplogroup in Europe,
having arrived from the Middle East as haplogroup IJ sometime between 40,000 and
30,000 years ago. There are two main subgroups, I1-M253
(Scandinavian origin) and I2-M438 (Central
and SE Europe origin).
I1-M253 is estimated to
have branched off and dispersed from the area of the northern Germany area below
the Jutland Peninsula of Denmark, possibly about 5,000 years ago.
I1 would have been the first to penetrate into Scandinavia
during the farming transition that lasted from about 4,200 to 2,300 BC.
The
largest concentration of those from the I1 Haplogroup appear in the
Scandinavian countries of Denmark, Sweden (particularly Gotland) and Norway,
and to a lesser extent in parts of Finland, northern Germany, Poland, the Low
Countries (Netherlands, Belgium), Britain, Ireland, France, Switzerland, the
Baltic countries, parts of Russia, and the Balkans.
The
Haplotree for the Y-DNA Haplogroup I and its subclades, as of 2016, produced by ISOGG
(International Society for Genetic Genealogists) can be seen at:
http:www.isogg.org/tree/ISOGG_HapgrpI.html
The
remainder of western and central Europe, Britain, and Ireland
are concentrated in the R1b Haplogroup.
As Britain, peopled by the early Celts and Britons, was invaded by Romans,
Angles, Saxons, Danes, Vikings and Normans, the majority of those of long British
heritage are a mixture of the two Haplogroups, with R1b (and its
subgroups) the most common, and I1 found in greater numbers in the Danelaw settlement areas
of Great Britain, and around York and Eastern Scotland, the western isles such as the Hebrides, and in parts of SE
Ireland including Dublin which were subject to Viking and Norman invasion. The
Celtic regions of Wales, SW England, Ireland and Scotland have a high
percentage of people in the R1b Haplogroup.
The following website gives information on the breakdown of
Haplogroups within Europe, based on the limited number of tests that have so
far been analysed for each area (constantly updated as the number of tests
increase):
http://www.eupedia.com/europe/european_y-dna_haplogroups.shtml
The newly developing science of genealogical Y-DNA matching will probably gain momentum in the coming years and may play an important role in unraveling these family tree mysteries and help with matching family links. It may also pose new unanswerable genealogical questions as well. DNA can provide information about our ancestor's migratory paths through thousands of years as well as individual descent from one's forebears. The same DNA markers are handed down from generation to generation for hundreds even thousands of years, with occasional mutations of individual markers in the DNA profile. A recent example was the use of DNA matching to identify the remains of King Richard III whose bones were found in a carpark in Leicester. Also the remains of the Russian Imperial family, murdered by the Bolshevics in 1917, were identified using Prince Philip's DNA (through his mother) and the Y-DNA of a Russian Count living in France. Two types of DNA testing were used in these cases- Y-DNA passed down through the male line (from father to son) and Mitochondrial DNA (mtDNA) passed down through the female line (although mtDNA is passed from the mother to both male and female children, only the female child can pass it onto her children).
A Haplogroup is defined as a genetic population group of people, or, a group of similar haplotypes that share a common ancestor on the patrilineal or matrilineal line;
It is like a pedigree chart of the different clans of humans throughout the world.
The earliest haplogroups were found in Africa. As people moved away from Africa and crossed into Asia and Europe and then spread further into the Americas, Australasia, etc, they developed unique mutations in their genetic code that would give rise to the various human clans worldwide, dating back tens of thousands of years ago. A new haplogroup is formed when a specific new mutation occurs in a chromosome of an individual, and all descendants carry that mutation.
With each mutation, called a Single Nucleotide Polymorphism, or 'SNP' for short, a subgroup or subclade of the original haplogroup begins a new haplogroup. As more and more haplogroups are rapidly being discovered as more SNP's downstream are discovered, the old letter numbering system is becoming unwieldly and will probably change, and may give way to the label of the lowest branch, or terminal SNP, to identify one's haplogroup, eg. Haplogroup 'I- L813' means original haplogroup 'I' (originating in northern Europe around 25,000 years ago) and subclade terminal SNP 'L813' which indicates a single ancestor with a unique mutation living about 1700 years ago in Norway. This subclade will be further refined as more SNP's are discovered 'downstream' of L813, and the time-frame of the most recent ancient ancestor is reduced further, giving rise to a new terminal SNP.
How are Recent and Ancient Ancestry determined, and what are STR
and SNP mutations?
As mentioned, Y-DNA is only present in males and is passed
down from father to son, as only the male child inherits the Y chromosome from
his father, and this information can reveal information on the patrilineal line
and determine one’s ancestral roots. The Y chromosome is passed down almost completely unchanged, although changes or mutations occur every couple of generations and those mutations are also passed on, giving each male lineage a unique signature.
There are two types of mutations: the more frequent STR, and the rare SNP mutation, and these are explained in more detail below.
Human DNA consists of about 3 billion bases and more
than 99% of those bases are the same in all people.
In the nucleus of each cell, the DNA molecule is
packed into thread-like structures called chromosomes. Each chromosome is made
up of DNA, containing thousands of genes which contain the instructions for our
individual characteristics. Humans have 23 pairs of chromosomes: 22 pairs of
numbered chromosomes, and one pair of sex chromosomes, X and Y. Each parent
contributes one chromosome to each pair so that offspring get half of their chromosomes
from their mother and half from the father. Males have one X and one Y chromosome,
while females have two X chromosomes.
Your genome is made of DNA which contains four basic
building blocks or ‘bases’.
In scientific terms, the chemical structure of DNA
consists of four nitrogenous bases: Adenin (A), Thymine (T), Guanine (G) and
Cytosine (C).
DNA bases pair up with each other, A with T, and C with G to form units called
base pairs. Each base is also attached to a sugar molecule and a phosphate
molecule, which together are called a nucleotide.
A DNA strand is a string of Nucleotides joined together, and the Nucleotides are then arranged in two long strands that twist around one another, joining together to make base pairs, and form
a spiral called a double helix, looking like a ladder with the base pairs
forming the ladder’s rungs, and they only pair up in a specific way- A only pairs
with T, and G pairs only with C. Each strand has a backbone made of alternating
groups of sugar and phosphate groups.
The order of these bases is what determines DNA's instructions or genetic code, and the entire human genome contains about 20,000 genes.
A 'Single Nucleotide Polymorphism', or SNP mutation is a single, small change in your DNA code. A SNP happens when a single base pair, or nucleotide, at all known locations along the Y, switches to another nucleotide/base pair, by
mistake eg. a base switched from the Ancestral C to a G (ie. Derived). This mutation, or nucleotide/base at this location being a G, is then
inherited down to all male descendants of the man in whom it first occurred.
This type of mutation on a single position in Y-DNA is very, very rare and seldom changes back. It
points to a certain individual as your paternal ancestor, although his name,
exact lifetime and location remain unknown. The more people who have SNPs
tested within a group will eventually lead to more accurate estimates as to
when and where he must have lived. The further down the Haplogroup tree, the closer in time the mutation occurred, and, as more males test, the chance of finding a common ancestor within a closer time-frame, say within the past 1000 years, increases.
Mutations are estimated to occur on average, once in 100 to 150 years. the following chart (from one of the Haplogroup Projects) gives an example of age estimates of these mutations:
If the common ancestor had two sons, 1500 years ago, and each line incurred one mutation every hundred years, at the end of 1500 years the number of mutations between the two men would be approximately 30, which would show up in the descendants of the original common ancestor.
Understanding the Terms "Ancestral" and "Derived":
Ancestral= unmutated version of a SNP (a negative result on a SNP means it is 'ancestral')
Derived= mutated version of a SNP (a positive result on a SNP means it is 'derived').
eg.
If the ancestral state for SNP 1234 is G, and if you have G for that SNP you are ancestral; if it has changed to, eg. A, your value is derived.
If you are tested for the L813 SNP and the result is negative (L813-) that means your Y-DNA has the original non-mutated (ancestral) value at the position on the Y Chromosome where L813 is found ie. you are NOT in the L813 subclade. If you are tested for L813 and the result is positive (L813+), that means your Y-DNA has the mutated (derived) value at that position on the Y Chromosome, and therefore you ARE within the L813 subclade.
A STR is a 'Short Tandem Repeat', ie. a place in your DNA code where a letter sequence in a single strand is repeated, eg. AGTAAGTAAGTA is three repeats of the sequence AGTA. STR's have a much faster mutation rate, and when they change, it is an increase or decrease in the number of repeats. STR values change back more commonly, and can occur every couple of generations , passing on to male descendants.
Y-DNA testing involves the STR
(short tandem repeat), and sometimes, SNP
(single-nucleotide polymorphism) testing of the Y-chromosome. These tests can
provide insight into the recent (via
STRs) and ancient (via SNPs) genetic ancestry.
A Y-chromosome STR test
(of several markers) will reveal the ‘haplotype’,
which should be similar among all the direct male descendants of a male
ancestor.
SNP tests are used to assign people to a patrilineal Haplogroup, which defines a much larger
genetic population.
Mutation acts to diversify the Y chromosome types associated
with a particular surname, but its impact is relatively predictable. The
mutation rates of SNPs are low, so, within the time-frame of surnames in most
populations, the widely typed SNPs are not expected to undergo many mutations, and this can help sort out
our deep ancestry of thousands of years past.
By contrast, STRs mutate rapidly, so several mutations are relatively
likely to be observed in that surname time-frame (ie. 700 years), and even
within a few generations, with some markers
having faster mutation rates than others and are more likely to change
within the genealogical time frame of 15 generations (500 years) or less.
The following example illustrates the difference between SNP’s
and STR’s:
Example of STR and SNP mutations in a single DNA strand of nucleotides
STR mutation- When reading the Y-DNA chromosome above, the
number of repeats of ‘CTA’ is recorded as a STR marker value, for example, the marker
DYSxxx =5 repeats for Male 1; DYSxxx=6 for Male 2; and DYSxxx=7 for Male 3.
This change, or mutation, in the numbers of repeats can occur in
any generation.
‘Short tandem repeats’-STR’s (or 'microsatellites'), are tandemly repeated sequences of a repeating
unit of 1 to 4 ‘nucleotides’ long. The number
of times the unit is repeated in a given STR can be highly
variable, a characteristic that makes them useful as genetic markers, widely
used for kinship analysis. STR’s occur at thousands of
locations in the human genome and they are notable for their high mutation rate
and high diversity in the population.
STR markers are usually
identified with DYS and a three digit number eg. DYS393. The D stands for DNA,
the Y stands for the Y chromosome, and the S stands for ‘a unique segment’. (A few
markers are identified differently, eg. CDY, Y-GATA-H4, YCAII, etc.)
STR’s that have faster changing mutation rates are:
DYS385, DYS439, DYS458, DYS449, DYS464, DYS456, DYS576, DYS570, CDY, DYS413, DYS557,
DYS481, and DYS446.
The SNP mutation
occurs between Male 1 and Male 2 with ‘A’ instead of ‘T’ in the sequence. If Male 1 was
the original lineage with a marker of T following GTAC, then Male 2
has the SNP mutation of A and will be the
ancestor of a new lineage, or his descendant, ( Male 3 descends from the same ancestor as Male 2, with
a STR mutation of 7 repeats of CTA instead of 6). That ‘nucleotide’ mutation or
genetic variation, may remain unchanged for many hundreds or even thousands of
years before another SNP mutation occurs. Male 1 is classed as a different
subclade than Males 2 and 3.
Haplogroups and Subclades
making up a Haplotree
Haplogroups can be further divided into subgroups, called
subclades, as defined by a change in a SNP, each with their own branches of SNP
changes, which narrows down a place and time when the original ancestor of
one’s particular lineage lived. They refer to these branches as a mutation
occurring “downstream” from the line
of descent - eg., in the I1-M253, or M253+ tree, - the
DF29 and Z131 SNPs are two
different branches of the I1- M253 tree; DF29 has further branches, and so on, reducing the time-frame
of a shared ancestor, and predicted place of migration.
Further SNP divisions are being discovered all the time, so the
Haplotree continues to evolve.
Genetic tree of I1-M253,
as of 2016 (ISOGG)
Each branch in the tree is a SNP mutation
that has divided a subgroup or subclade, which has occurred over a time span of
thousands of years.
Laurence Butler’s proven haplogroup and subclades on this tree are marked in
red.
One of Laurence Butler's male descendants has done a Y-DNA test
(111 STR markers tested) and his Haplogroup (deep ancestral roots) was
confirmed as belonging to the I Haplogroup, I1 subclade, confirmed by the Single
Nucleotide Polymorphisms, ie. SNPs (mutations), known as M253, DF29, CTS6364, L22, Z74 and L813.In
2021, Laurence Butler’s Terminal SNP was FGC15301,
with 5 unique/Novel Variants (mutations), downstream
from Z74 and L813.
‘BIG Y’ DNA test by FamilyTreeDNA
With the Big Y DNA
test, your Y chromosome is completely tested and your haplogroup defined to the
most refined level possible, often called your ‘TERMINAL SNP’, and given your
position on the Y
TREE.
The Big Y sequences approximately 12 million base pairs of the Y chromosome, and identifies SNP results within those 12 million base pairs.
DNA scientists have learned an incredible amount about the human Y-DNA tree as a result of more and more men taking the Big Y test.
Your results of this test reveal various lists of positive
SNPs based on:
a) Whether the SNP’s are ANCESTRAL (inherited intact from distant ancestors thousands of
years ago) or DERIVED for a SNP (ie.
a SNP/mutation at some time by a more recent ancestor and no longer has ancestral value); these are listed as ‘NAMED VARIANTS’.
b)Whether it is on the established Y TREE (ie. at least two or three found with the same
mutation), which is growing constantly, as increasing numbers of males test
their BIG Y. As of the present (July 2018), the list of Named Variants in Big Y
includes 124,085 SNP’s.
c)And ‘NOVEL/UNNAMED VARIANTS’, which means there are
not yet enough males tested with this mutation to be listed on the Y Tree yet-
there could be thousands of people that have the same mutation that have not
tested their BIG Y, or, there could be just yourself with this SNP, or just a few
people, most probably closely related. Eventually all, or most, of these ‘Novel/Unnamed
Variants’ will hopefully be mapped to the Y-Tree.
d) ‘MATCHES’, which is a list of males who have
tested with BigY, and are found to have matched your SNP’s down to your
Terminal SNP, and therefore have a common ancestor at some point in time. They
may have further positive SNP’s downstream from your Terminal SNP, to which you
are negative, and therefore have a different branch on the Y Tree.
There are several separate Y-Trees being constructed: BIG Y TREE, plus those by third party
analysis companies such as FGC (Full
Genomes Corporation ) and YFULL, who
assign names to newly discovered SNP’s. If discovered by Big Y, the SNP begins
with the prefix BY (or L if found pre
the BigY tests) (eg. BY15746 at
position 7493637, Mutation A->G);
if discovered by Full
Genomes Corporation, the SNP starts with prefix, FGC (eg. FGC15301,
position 11713440, G->A);
and if by YFULL,
the SNP starts with prefix Y (eg. Y17060, position 12203189, C->A).
This increases the possibility of dual naming when
multiple entities name the same SNP about the same time. Eg. FGC15301 is also known as Y17060.
At this point, BY
and L prefixes have named 153,902
Novel Variants SNP’s; YFULL has named 133,571 Novel Variant SNP’s and FGC has
81,363 Novel Variant SNP’s, but these SNP’s do not go onto the YTree until a
second example (and non-family) is found with a good read (of 10 repeats or
more).
ISOGG (International Society of Genetic Genealogy)
also has a Y tree constructed using all of the above tree information.
A named branch may be defined by several SNP’s with
one chosen to name the branch. This changes when a discovery is made that will
further divide this branch into 2 or more branches. That’s how the tree is
built.
BIG Y Test of descendant of Laurence Butler
Haplogroup 'I' dates to 23,000 years
ago, or older. The I-M253 lineage likely has its roots in northern France.
Today it is found most frequently within Viking/Scandinavian populations in
northwest Europe and has since spread down into Central and Eastern Europe,
where it is found at low frequencies. Haplogroup I represents one of the first
peoples in Europe.
At this point (July 2021), the descendant of Laurence
Butler has been given a Terminal SNP of I-FGC15301, or, I-Y17060.
FTDNA’s REPORT:
Your
Confirmed Haplogroup is I-FGC15301
There is a separate branch downstream from FCG15301, named as FGC15300, or, I-Y20364This chart shows the
Y-tree branches off subclade I-L813 (which branches off I-Z74), including subclade I-Y5153/FGC15298 which in turn
branches off to subclade I-Y17060 which includes SNP FCG15301, viz. Laurence
Butler’s terminal SNP.
I-Y17060 further branches
off to subclade I-Y20364 which includes SNP FGC15300, the terminal SNP of two
descendants of a man named Hicks (see below).
(Terms:
ybp= years before present (averaged given a 600
to 800 year range)
TMRCA=
The Most Recent Common Ancestor (of everyone who has tested for a given
haplogroup)
YDNA BIG Y Test matches
Out of all the millions of Big-Y tests conducted so far, there is only one other match for Laurence Butler's terminal SNP of FGC15301. He is identified as a descendant of a man named Henry Atkins, born 1718 and died 1786, from Kent in England.
Notably, this does not mean that the Butlers are really Atkins descendants, or that the Atkins are really Butler descendants. They do share a common ancestor, but in a period of time, hundreds of years before the general use of surnames.
Two descendants of a male ancestor named Hicks, Thomas Hicks from England c 1598-1653 who migrated to the Plymouth Colony USA, and the other ancestor Joseph Hicks 1765-1800 lived in Ontario Canada- their terminal SNP is downstream from Butler and Atkins, meaning their ancestor developed a new SNP after their shared common ancestor with Laurence, and is named FGC15300.
On the chart above, YFULL gives an estimate of ancestors back in time. They are measured using the terms, 'ybp' = 'Years Before Present' (using the standard, January 1, 1950; averaged given a 600-800 year range), and the term 'TMRCA' = 'Time of the Most Recent Common Ancestor', which depends on the number of testers testing positive for that particular SNP, and an analysis of their STR mutations.
The following quotes are from FTDNA Forums:
“The core of
each calculation is a mathematical formula that references how to estimate the
date range based on the mutation rate of the changes in STR’s. Each male
inherits his father’s SNPs and STRs of their male lineage; a SNP mutation
occurs in a single man and is inherited by his descendants and not found in his
father or male siblings. It is one of the best ways to trace the male ancestry
especially since the STR mutations are predictable and are unchanged being an
excellent means of dating the occurrence of SNPs. The way the STRs calculate
the SNP date range is called finding the Time to the Most Recent Common Ancestor
or TMRCA.”
“The formed and TMRCA dates are just estimates and
they are based on an average mutation of one SNP every 144.41 years and
an assumed age of 60 years for living providers of YFull samples. On average, one
male generation is 32.5 years which is about 4.44 generations permutation.
The estimated age of a subclade that is several thousands of years old isn’t going
to be miscalculated to be thousands of years older or younger than it actually
is. It will be off by a few hundred and that is as close as we can get with
current testing and participation rates.”
YFULL estimates that the 'most recent common ancestor' for I-Y17060 (ie. FGC 15301) to be formed approximately 2100 ybp, TRMCA 1500 ybp, whereas I-Y20364 (ie. FGC15300) formed 1500 ybp and TRMCA about 400ybp.
The SNP from which they branched off, I-Y5153 (SNP FGC15298) branched off the I-L813 SNP about 2100 TMRCA ybp which branched off Z74 about 3100 TMRCA, and Z74 branched off L22 about 3900 TMRCA ybp.
FTDNA's Y HAPLOGEOUP TREE
However, FamilyTreeDNA has analysed their data to make their own estimated haplogroup origin time range for TMRCA which is calculated based on SNP and STR test results from DNA testers, which is represented in this 'probability plot', showing the most likely time when the common ancestor was born amongst the other statistical possibilities:
bce= 'before common era'; ce= 'common era'- used exactly the same as traditional Latin abbreviations BC and AD.
They have also applied the information to make a
haplogroup origin tree and timeline for this subclade:
This shows a divergence of FGC15301 from FGC15298 between about 300
BC and 800 AD, with the Hicks SNP of FGC15300 diverging from FGC15301 between
1200 AD and1800 AD.
The SNP chart (FTDNA) shows the identified SNPs unique
to that particular terminal SNP.
Laurence has 5 Unnamed/Novel Variants unique to
him, that do not as yet match with any other person who has tested, including
Atkins who has his own Unnamed Variants (ie. 9). When a second positive test match
occurs with these Unnamed Variants, they become a ‘Named Variant’, and the
terminal SNP may change.
A FTDNA Forum explained:
“Each ‘reliable’ SNP appears to correspond to 140-150
years of patrilineage.
If you are determined to have 11 novel SNPs, then you
and the nearest other tester share a MRCA roughly 1540-1650 years ago.”
Using that calculation, Laurence Butler, with 5 Novel
SNPs, and Atkins with 9 Novel SNP's should share an ancestor about 1300 years ago.
The Atkins descendant, has 688569 Shared Variants with
Laurence Butler’s descendant, and 26 Non-Matching
Variants.
The Hicks descendant has 425,415 Shared Variants
with Laurence Butler and 30 Non-Matching Variants.
FTDNA- BIG Y test- two listed matches
between Laurence Butler and 1. Atkins, and 2. Hicks. Butler’s Y-DNA SNP matches showing Non-Matching Variants and the numbers of Shared Variants:
1. ATKINS
(NB. SNP's 7493637, 7924151, 14858373, 20781736 and 26658532 are Butler's Novel SNPs, and 20766127, 21221496 and 22225420 are Atkins' Novel SNP's
2. HICKS
Chart
1= Atkins’ descendant, and Chart 2 = Thomas Hicks’ descendant (which shows that
the particular SNP FGC15300 is listed in Non-Matching Variants with Butler). Interestingly, Atkins and Hicks share SNPs L431, L432, L433, L434, L435, which do not match with Butler. This would seem to indicate that the Hicks branched off the Atkins branch later than with Butler.
(NB. for some unknown reason, FTDNA analysts have not put Butler's Novel SNP's in the Hicks list of non-matching variants, so maybe that list should have 5 more than stated)
The I-L813 Y-DNA Project (FTDNA) has Butler,
Atkins, and Hicks, grouped as follows, showing their SNP progression from L813,
and their Terminal SNP:
STR Mutations (Notably, STR
mutations occur more frequently than SNP mutations- a generation is calculated at about 31 years)
The following chart (from one of the Haplogroup Projects) gives an example of age estimates of mutations which occur, on average, once in 100 or 150 years.
If a common ancestor had two sons, 1500 years ago, and each line incurred 1 mutation every hundred years, at the end of 1500 years the number of mutations between the men would be approximately 30, which would show up in the descendants of the original common ancestor.
The following chart shows the STR markers of
Laurence Butler, Henry Atkins, Thomas Hicks and Joseph Hicks, and where the
individual marker mutations occur. Notably there are mutations between the two
Hicks descendants as well, indicating more recent mutations:
Looking at, and comparing the STR marker values for
the Butler and Hicks’ descendants, there are 19 variations in the STR markers
(92 matching out of 111 markers) between the Butler descendant and Thomas Hicks’
descendant, and a slightly different 16 variations between Butler and Joseph
Hicks’ descendant (95 out of 111 markers). Using the mutation rate chart above, this approximates a common ancestor about 800-1000 years ago.
The Atkins and Butler STR Markers show 17 variations
(ie. 94 out of 111 markers), similar to the Hicks. Using the mutation rate chart above, this approximates a
common ancestor about 800-900 years ago.
It should be noted that there are many variables,
including the rate of mutation by each lineage, that can make a much wider
margin of error.
The following chart shows the
variants in the STR markers between Butler and Atkins, marked by a red star. Two stars mark variants of 2 in the same marker.
As the FTDNA learning centre explains about genetic distance for 111 markers:
The 'genealogical time-frame' is considered about 700 years.
Haplogroup Geographical
Origins
Haplogroup ‘I’, subclade ‘I1’, geographically, is highly concentrated
in Nth Germany, Denmark, Sth Norway and Sth Sweden.
A new study in 2015 estimated the origin of I1-M253 between 3,470 to 5,070
years ago or between 3,180 to 3,760 years ago, using two different techniques.
It is suggested that it initially dispersed from the area that is now Jutland
in Denmark and Holstein in adjacent NW Germany, although the Haplo I expert Dr. Ken Nordvedt, has now suggested
that I1 possibly originated in the ancient Old Prussia
territory, or Pomerania (a region on the Baltic Sea split between Germany and
Poland). The Danish and Norwegian Vikings brought I1 to Britain, Ireland, the Isle of Man, Normandy, Flanders, and
Iberia (Spain, Portugal, Andorra) in the 9th and 10th
centuries.
However, there is still great debate on the estimated ages of
these subclades. The names of subclades continually change as new markers are
discovered which clarify the sequence of branchings of the I tree. Subclade Z74 is one such recently identified subclade.
Subclades
L22+ and the later Z74 are Norse, founders having lived up in Scandinavia. Z74 is further divided
into the L287
branch which is predominantly Finnish (using SNP CTS2208 to confirm or negate),
and L813
which spread NW into Norway and via the Vikings into Britain, SE Ireland, and
the Nth Netherlands area, and probably the Normandy area.
It has been observed that Haplogroup I decreases in Britain when moving east to west,
influenced by the Danish Vikings settling in the Danelaw areas of the eastern
counties, and that the Norwegian Viking invaders influenced the northern area of Britain around York, and including
mainland Scotland in the east and the western Isles
How Haplogroups and subclades have specific STR marker values in
common
The human genome is full of repeated
DNA sequences coming in various sizes.
The Y-DNA test creates a Y-DNA signature or haplotype using the
Y-chromosome STR Markers, which can be compared with the
Y-DNA signature of others.
All men with the I1- M253 Y-chromosome SNP share a common ancestor, and all of
their STR markers can be expected to
be in a range around that of their forefather.
The 111 STR markers of Laurence Butler’s descendant can be seen
in the STR results chart below. Each STR marker is numbered, eg. DYS 393, and
given a value of repeats, eg. 13.
Certain STR Markers (and their ‘repeat values’) indicate
belonging specifically to the I1 Haplogroup.
Varieties of I1 have been defined by Dr. Ken Nordtvedt
based on STR haplotypes:
DYS455 = repeat value
8, is virtually
exclusive to I1. Most males have a value of 11 at this
marker and the deletion to 8 is believed to have taken place about 5000 years
ago. (Laurence’s descendant’s
TEST= 8)
DYS511 has a value of
10 in Norse and
Ultra-Norse varieties, but have a value
of 9 in Anglo Saxon varieties. (descendant’s TEST=10)
DYS462 is similarly useful- value 13 in Norse, and value
12 in Anglo-Saxon varieties. (descendant's TEST= 13)
YCAII is universally
19, 21 for I1 (descendant's TEST= 19, 21)
DYS388 = value 14 (Test=14)
DYS437 = value16 (Test=16)
The website http://www.eupedia.com/europe/Haplogroup_I1_Y-DNA.shtml, is worth reading for information on the
history of this haplogroup.
Grouping by STR:
All Germanic tribes expanded from a small geographic core around
Denmark and Southern Sweden. STR variations allow the division of I1 members into various categories.
There are two main clusters, each with their own subgroups:
The NORTHERN CLUSTER:
peaking in Norway, Sweden and Finland, which corresponds to the
I1a2 (L22+) subclade, normally has an STR value
greater than 22 for DYS390 (descendant's TEST= 23)
-the NORSE group corresponds to Ken
Nordtvedt’s Norse (mostly Swedish, and smaller quantities in Finland,
Norway and Denmark) and ULTRA-NORSE (mostly Norwegian and Icelandic, smaller
quantities in Sweden and Denmark) haplotypes:
STR's: DYS 390 greater
than 22 (Test =23); DYS
511 greater than 9 (Test =10); DYS617
less or equal 13 (Test=13); DYS 462 =13 (Test 13)
The Ultra-Norse
haplotype I (ie. I1-uN1) differs from the Norse by
having DYS385b=15 and
usually DYS449=29 (descendant's TEST: DYS385=13-14; DYS449=28); DYS19=14 (Test=14); DYS 390 =23 (Test =23), DYS 385=14-15 (Test =13,14), DYS462=13 (Test=
13)
-The BOTHNIAN
group is found
mostly in Finland and NE Sweden, bordering the Gulf of Bothnia. Western Finland
STR's: DYS390 greater than 22 (Test=23); DYS511 less or equal 9
(Test=10); DYS
462=13 (Test=13) ; DYS458 less or equal 15
(Test =16); DYS439=10, (Test=11) DYS385=
14,14 (Test= 13,14) DYS464d=15 (Test=16)
The SOUTHERN CLUSTER:
mostly in Denmark, Germany, the Low Countries and the British
Isles.
-The Danish/Polish group usually has a DYS557 value greater than 15 (descendant's TEST= 15)
-The Western Group/Anglo-Saxon, comprising the Low Countries, England,
Scotland, and Ireland, matches the Z58+ subclade. It probably matches Anglo-Saxon and Frisian/Batavian
ancestry (notably marked by DYS 511=9;
DYS462 =12; descendant’s Test =10, 13).
There appears to be a
specific Welsh subgroup defined by a GATA-H4 value superior or equal to 11 (descendant's TEST=10)
-The German group is the most common type of I1 in Germany, France, Italy and Central Europe,
but is also found in the British Isles and to a lower extent in Scandinavia. It
is defined by a DYS456 value
inferior to 15. It corresponds to the Z63+ subclade. (descendant's TEST= 14)
NB. DYS462 and DYS511 are two markers that mutate very rarely.
Refer to the 'I haplogroup, subclade I1 Project'-
https://www.familytreedna.com/public/yDNA_I1):
The L22+/Norse/ultra Norse subclades have also been given a further
breakdown, with the predicted time of the most recent common ancestor:
(ref: https://www.familytreedna.com/public/I1d/default.aspx?section=results)
M253-uN1315 (ultra-Norse 13 15)- about 3500 years (the
first to carry the mutation known as I1)
L22-N (Norse)- about 3000 years ago (I1-L22 Norse
was born- the first to carry the mutation known as I1d- ie DYS462=13, DYS 511
=10)
L22-NuN14 (Norse ultra-Norse)- about 2750 years ago
L22-uN1 (ultra-Norse type 1)- about 2550 years ago
(now concentrated in Sweden)
L22-uN2 (ultra-Norse type 2)- about 1570 years ago
(now concentrated in Norway)
L22-uN9 (ultra-Norse type 9)- about 1800 years ago
(now concentrated in Sweden)
L22-uN9a (ultra-Norse type 9a)- about 1450 years ago
(now concentrated in Sweden)
L22-Bothnian- about 1850 years ago- still have the value 9
for DYS511 (now concentrated in Sweden/Finland)
Laurence Butler’s Deep
Ancestral Origins
The L22+ subclade is
from the Northern Cluster- Norse group, and appeared about 3000 years ago..
The website
http://www.eupedia.com/europe/Haplogroup_I1_Y-DNA.shtml, has the
following explanation of the subclade L22:
L22+ is the main Nordic subclade. It is also very
common in Britain, especially on the east coast where the Vikings settled most
heavily, in the Low Countries and Normandy (also doubtlessly the heritage of
the Danish Viking), as well as in Poland and Russia (Swedish Vikings). The L22
subclade is further divided into P109+
(all regions settled by the Danish Vikings), L205+ (mostly limited to the Low Countries, France and Britain), L300+ (almost exclusively southern
Finland), and the Z74 branch divides into L287 (predominantly Bothnian- test CTS2208)
and L813 (predominantly Scandinavian- common in southern Norway, and
in Britain and northern Netherlands, but not Germany). (NB. ‘SNP L813’ determined by a SNP mutation
in Y chromosome position 7719777 from an ancestral base A changing to a new ancestral base G, found in L22- ultra Norse people).
There are two types of mutations: the more frequent STR, and the rare SNP mutation, and these are explained in more detail below.
DNA bases pair up with each other, A with T, and C with G to form units called base pairs. Each base is also attached to a sugar molecule and a phosphate molecule, which together are called a nucleotide.
A DNA strand is a string of Nucleotides joined together, and the Nucleotides are then arranged in two long strands that twist around one another, joining together to make base pairs, and form a spiral called a double helix, looking like a ladder with the base pairs forming the ladder’s rungs, and they only pair up in a specific way- A only pairs with T, and G pairs only with C. Each strand has a backbone made of alternating groups of sugar and phosphate groups.
Understanding the Terms "Ancestral" and "Derived":
Ancestral= unmutated version of a SNP (a negative result on a SNP means it is 'ancestral')
Derived= mutated version of a SNP (a positive result on a SNP means it is 'derived').
eg.
If the ancestral state for SNP 1234 is G, and if you have G for that SNP you are ancestral; if it has changed to, eg. A, your value is derived.
If you are tested for the L813 SNP and the result is negative (L813-) that means your Y-DNA has the original non-mutated (ancestral) value at the position on the Y Chromosome where L813 is found ie. you are NOT in the L813 subclade. If you are tested for L813 and the result is positive (L813+), that means your Y-DNA has the mutated (derived) value at that position on the Y Chromosome, and therefore you ARE within the L813 subclade.
Laurence Butler’s proven haplogroup and subclades on this tree are marked in red.
In 2021, Laurence Butler’s Terminal SNP was FGC15301, with 5 unique/Novel Variants (mutations), downstream from Z74 and L813.
The Big Y sequences approximately 12 million base pairs of the Y chromosome, and identifies SNP results within those 12 million base pairs.
DNA scientists have learned an incredible amount about the human Y-DNA tree as a result of more and more men taking the Big Y test.
Haplogroup 'I' dates to 23,000 years
ago, or older. The I-M253 lineage likely has its roots in northern France.
Today it is found most frequently within Viking/Scandinavian populations in
northwest Europe and has since spread down into Central and Eastern Europe,
where it is found at low frequencies. Haplogroup I represents one of the first
peoples in Europe.
This chart shows the
Y-tree branches off subclade I-L813 (which branches off I-Z74), including subclade I-Y5153/FGC15298 which in turn
branches off to subclade I-Y17060 which includes SNP FCG15301, viz. Laurence
Butler’s terminal SNP.
I-Y17060 further branches
off to subclade I-Y20364 which includes SNP FGC15300, the terminal SNP of two
descendants of a man named Hicks (see below).
(Terms:
ybp= years before present (averaged given a 600
to 800 year range)
TMRCA=
The Most Recent Common Ancestor (of everyone who has tested for a given
haplogroup)
YDNA BIG Y Test matches
Out of all the millions of Big-Y tests conducted so far, there is only one other match for Laurence Butler's terminal SNP of FGC15301. He is identified as a descendant of a man named Henry Atkins, born 1718 and died 1786, from Kent in England.
Notably, this does not mean that the Butlers are really Atkins descendants, or that the Atkins are really Butler descendants. They do share a common ancestor, but in a period of time, hundreds of years before the general use of surnames.
Two descendants of a male ancestor named Hicks, Thomas Hicks from England c 1598-1653 who migrated to the Plymouth Colony USA, and the other ancestor Joseph Hicks 1765-1800 lived in Ontario Canada- their terminal SNP is downstream from Butler and Atkins, meaning their ancestor developed a new SNP after their shared common ancestor with Laurence, and is named FGC15300.
On the chart above, YFULL gives an estimate of ancestors back in time. They are measured using the terms, 'ybp' = 'Years Before Present' (using the standard, January 1, 1950; averaged given a 600-800 year range), and the term 'TMRCA' = 'Time of the Most Recent Common Ancestor', which depends on the number of testers testing positive for that particular SNP, and an analysis of their STR mutations.
The following quotes are from FTDNA Forums:
“The core of
each calculation is a mathematical formula that references how to estimate the
date range based on the mutation rate of the changes in STR’s. Each male
inherits his father’s SNPs and STRs of their male lineage; a SNP mutation
occurs in a single man and is inherited by his descendants and not found in his
father or male siblings. It is one of the best ways to trace the male ancestry
especially since the STR mutations are predictable and are unchanged being an
excellent means of dating the occurrence of SNPs. The way the STRs calculate
the SNP date range is called finding the Time to the Most Recent Common Ancestor
or TMRCA.”
“The formed and TMRCA dates are just estimates and they are based on an average mutation of one SNP every 144.41 years and an assumed age of 60 years for living providers of YFull samples. On average, one male generation is 32.5 years which is about 4.44 generations permutation. The estimated age of a subclade that is several thousands of years old isn’t going to be miscalculated to be thousands of years older or younger than it actually is. It will be off by a few hundred and that is as close as we can get with current testing and participation rates.”
YFULL estimates that the 'most recent common ancestor' for I-Y17060 (ie. FGC 15301) to be formed approximately 2100 ybp, TRMCA 1500 ybp, whereas I-Y20364 (ie. FGC15300) formed 1500 ybp and TRMCA about 400ybp.
The SNP from which they branched off, I-Y5153 (SNP FGC15298) branched off the I-L813 SNP about 2100 TMRCA ybp which branched off Z74 about 3100 TMRCA, and Z74 branched off L22 about 3900 TMRCA ybp.
FTDNA's Y HAPLOGEOUP TREE
However, FamilyTreeDNA has analysed their data to make their own estimated haplogroup origin time range for TMRCA which is calculated based on SNP and STR test results from DNA testers, which is represented in this 'probability plot', showing the most likely time when the common ancestor was born amongst the other statistical possibilities:
bce= 'before common era'; ce= 'common era'- used exactly the same as traditional Latin abbreviations BC and AD.
They have also applied the information to make a
haplogroup origin tree and timeline for this subclade:
This shows a divergence of FGC15301 from FGC15298 between about 300
BC and 800 AD, with the Hicks SNP of FGC15300 diverging from FGC15301 between
1200 AD and1800 AD.
The SNP chart (FTDNA) shows the identified SNPs unique to that particular terminal SNP.
Laurence has 5 Unnamed/Novel Variants unique to
him, that do not as yet match with any other person who has tested, including
Atkins who has his own Unnamed Variants (ie. 9). When a second positive test match
occurs with these Unnamed Variants, they become a ‘Named Variant’, and the
terminal SNP may change.
A FTDNA Forum explained:
“Each ‘reliable’ SNP appears to correspond to 140-150
years of patrilineage.
If you are determined to have 11 novel SNPs, then you
and the nearest other tester share a MRCA roughly 1540-1650 years ago.”
Using that calculation, Laurence Butler, with 5 Novel SNPs, and Atkins with 9 Novel SNP's should share an ancestor about 1300 years ago.
The Atkins descendant, has 688569 Shared Variants with Laurence Butler’s descendant, and 26 Non-Matching Variants.
The Hicks descendant has 425,415 Shared Variants with Laurence Butler and 30 Non-Matching Variants.
FTDNA- BIG Y test- two listed matches between Laurence Butler and 1. Atkins, and 2. Hicks. Butler’s Y-DNA SNP matches showing Non-Matching Variants and the numbers of Shared Variants:
1. ATKINS
Chart 1= Atkins’ descendant, and Chart 2 = Thomas Hicks’ descendant (which shows that the particular SNP FGC15300 is listed in Non-Matching Variants with Butler). Interestingly, Atkins and Hicks share SNPs L431, L432, L433, L434, L435, which do not match with Butler. This would seem to indicate that the Hicks branched off the Atkins branch later than with Butler.
(NB. for some unknown reason, FTDNA analysts have not put Butler's Novel SNP's in the Hicks list of non-matching variants, so maybe that list should have 5 more than stated)
The I-L813 Y-DNA Project (FTDNA) has Butler,
Atkins, and Hicks, grouped as follows, showing their SNP progression from L813,
and their Terminal SNP:
STR Mutations
The following chart (from one of the Haplogroup Projects) gives an example of age estimates of mutations which occur, on average, once in 100 or 150 years.
If a common ancestor had two sons, 1500 years ago, and each line incurred 1 mutation every hundred years, at the end of 1500 years the number of mutations between the men would be approximately 30, which would show up in the descendants of the original common ancestor.
The following chart shows the STR markers of Laurence Butler, Henry Atkins, Thomas Hicks and Joseph Hicks, and where the individual marker mutations occur. Notably there are mutations between the two Hicks descendants as well, indicating more recent mutations:
Looking at, and comparing the STR marker values for
the Butler and Hicks’ descendants, there are 19 variations in the STR markers
(92 matching out of 111 markers) between the Butler descendant and Thomas Hicks’
descendant, and a slightly different 16 variations between Butler and Joseph
Hicks’ descendant (95 out of 111 markers).
The Atkins and Butler STR Markers show 17 variations (ie. 94 out of 111 markers), similar to the Hicks. Using the mutation rate chart above, this approximates a common ancestor about 800-900 years ago.
It should be noted that there are many variables,
including the rate of mutation by each lineage, that can make a much wider
margin of error.
The following chart shows the variants in the STR markers between Butler and Atkins, marked by a red star. Two stars mark variants of 2 in the same marker.
As the FTDNA learning centre explains about genetic distance for 111 markers:
It has been observed that Haplogroup I decreases in Britain when moving east to west, influenced by the Danish Vikings settling in the Danelaw areas of the eastern counties, and that the Norwegian Viking invaders influenced the northern area of Britain around York, and including mainland Scotland in the east and the western Isles
The Ultra-Norse haplotype I (ie. I1-uN1) differs from the Norse by having DYS385b=15 and usually DYS449=29 (descendant's TEST: DYS385=13-14; DYS449=28); DYS19=14 (Test=14); DYS 390 =23 (Test =23), DYS 385=14-15 (Test =13,14), DYS462=13 (Test= 13)
NB. DYS462 and DYS511 are two markers that mutate very rarely.
Laurence Butler’s Deep Ancestral Origins
L22+ is the main Nordic subclade. It is also very common in Britain, especially on the east coast where the Vikings settled most heavily, in the Low Countries and Normandy (also doubtlessly the heritage of the Danish Viking), as well as in Poland and Russia (Swedish Vikings). The L22 subclade is further divided into P109+ (all regions settled by the Danish Vikings), L205+ (mostly limited to the Low Countries, France and Britain), L300+ (almost exclusively southern Finland), and the Z74 branch divides into L287 (predominantly Bothnian- test CTS2208) and L813 (predominantly Scandinavian- common in southern Norway, and in Britain and northern Netherlands, but not Germany).
Conclusion on the ancient ancestry of Laurence Butler
The above information indicates that
Laurence’s descendant comes from the Northern Cluster of Norse haplotypes (I1-L22, Z74+, L813), and L22- uN2 (ultra Norse type
2 ), which means Laurence and his descendants are probably
of Norwegian Viking heritage.
Interestingly, the first of the Butler line in Ireland was Theobald Walter, and
Theobald’s grandfather Hervey and father Hervey Walter were granted lands in
Weeton, Lancashire and also held lands in East Anglia, Norfolk & Suffolk in
1130 which are in the Danelaw areas. The name 'Hervey', derived from the French 'Herve', arrived in England with the Norman Conquest of 1066. It is a name of ancient Norman or Breton origin, from the Breton given name Haerviu, meaning 'battle worthy'.
Hervey the elder (no surnames in England at
this point) is supposed to have been a son or grandson of a Norman who accompanied William
the Conqueror to England in 1066, identity unknown at this stage.
The Normans first settled in the area of
France named Normandy in around 918 by the leader of a group of Viking settlers, named Rollo (c.846-c.932), who supposedly came from a noble warrior
family of Scandinavia. Legends say that Rollo sailed off to Scotland, Ireland, England and
Flanders on pirating expeditions before settling on Frankish soil in the valley
of the lower Seine. The King of West Francia ceded them lands between the mouth
of the Seine and the city of Rouen in return for protection against further
incursion by Norse bands. This became the Duchy of Normandy which was ruled by
Rollo’s descendants. William the Conqueror, Duke of Normandy and King of England, was 3x great grandson of Rollo, and his many Norman followers were mostly descendants of this original Viking band.
However,
not all of William’s followers were necessarily Normans. The historian, Gwyn Jones ['History
of the Vikings'] makes it clear that:
although Danes formed the bulk of Rollo's band, there were Anglo-Danes from the
Danelaw amongst them, some Hiberno-Norse, a few Swedes and a small Norwegian
contingent that allegedly settled the Cotentin (peninsula on NW coast of France
extending into the English Channel towards Great Britain, near the Channel
Islands) in the 9th and 10th centuries. Duke William
recruited from the whole of northern France with some outliers. The bulk of his
invasion force of 1066 were 'native Norman' but these men would not be
Scandinavian on all lines due to intermarriage with women of the Gallo-Frankish
culture. The second largest contingents were from Flanders and Brittany. Other
areas of recruitment were Ile De France, Gascony etc. The invasion force of
1066 was, far from being 'Danish', something of a mixed Celto-Germanic bag-
native Normans, Bretons, Flemings, Franks, Gascons etc.
During the 9th century, Ireland
was attacked by Viking raids and a Viking longport (Viking ship enclosure along rivers, or a shore fortress)
was established at Dublin. Most of the early raiders came from the fjords of
western Norway, under the leadership of Olaf and his kinsman Ivar. They entered
into alliances with various Irish rulers. Their descendants were forced to
leave Dublin in 902, but remained active around the Irish Sea. A new Viking
fleet appeared in Waterford Harbour in 914 and another near Leixlip in
Leinster, and regained control of Dublin. Some of these were Danish Vikings. A
more intensive period of settlement in Ireland began, with Viking longports established at Dublin,
Wexford, Waterford, Cork and Limerick which became the first large towns in
Ireland, and they founded many other coastal towns. Wexford in pre-Norman times was part of the Kingdom of UÃ Cheinnselaig, with its capital at Ferns. The first recorded raid by the Vikings in Co. Wexford occurred in 819, and in 835 Ferns was plundered. In 839 and 919 Ferns was burned by the Vikings. At least as early as 888, the Vikings had established a separate settlement of some sort at Wexford Town, known then as Loch Garman by the Irish, and in 919 "the foreigners of Loch Garman" are mentioned, and again in 1088. The original separate Viking settlement was named 'Waesfjord' by the Vikings (meaning 'inlet or fjord of the mudflats', in old Norse language). The two separate settlements eventually merged to become Wexford Town.
After several generations
of coexistence and intermarriage, a group of mixed Irish and Norse ethnic
background arose, which shows in the DNA evidence in some residents of these
coastal cities, particularly in Wexford, to this day.
Laurence Butler’s Norse DNA ancestry could be
attributed to either of the above scenarios- as a direct descendant of Theobald
Walter, a Norman knight who arrived in Co. Wexford in Leinster when King Henry
II invaded in 1171, and was granted the hereditary title 'Chief Butler of Ireland', hence the origin of the surname 'le Botelier' or 'Butler' in Ireland; or a direct descendant of one of the Viking settlers in Leinster,
particularly Wexford, dating back to the 9th or 10th
centuries, and having acquired the Butler surname, possibly through a marriage
alliance, sometime down the centuries that followed.
Laurence Butler's 'Recent Ancestry' and Y-DNA
Haplotype Signature
To prove that the results of the Y-DNA test done on the descendant of Laurence
Butler makes up Laurence Butler's Y-DNA haplotype signature, a Y-DNA test was conducted on
a descendant of each of Laurence Butler's two sons, viz. Walter
Butler (b. 1807 Sydney, to Mary Ann Fowles) and Lawrence Butler Junior
(b.1812 Sydney, to Ann Roberts).
These Y-DNA results
can be viewed on the Butler Surname Y-DNA Project website
at FamilyTreeDNA under the name of ancestor Laurence Butler b.1750 Wexford, Ire.
The Y-DNA tests were
conducted by Family Tree DNA at www.familytreedna.com
https://www.familytreedna.com/group-join.aspx?Group=Butler
The descendant of Walter Butler (by 1st wife Margaret Dunn) had 111 STR markers tested and is 7th generation down from Laurence Senior;
and the descendant of Lawrence Butler Junior (by 1st wife Catherine Gorman)
had 67 STR markers tested, and is also 7th generation.
The test results for various levels show that the two
descendants match exactly for the first 25
markers; for 36 out of 37 markers; and for 64 out of 67 markers, with three
mutations, which is defined as a Genetic Distance of 3; and they have the same HAPLO group ( I1- M253). Also,
it should be noted that the 111 marker STR test done by the descendant of Henry
Atkins, as previously analysed, shows that, of the three marker changes above,
one occurred in Walter’s descendant lineage and two occurred in Lawrence Jnr’s descendant lineage.
Historically, it should also be taken into account that when
Walter (b.1807) and Lawrence Jnr (b.1812) were born, the colony of New South
Wales had a population of only a few thousand, many of whom lived outside of
Sydney, whereas Laurence Butler Snr lived in Sydney. This small population statistic can
be further divided by gender, age, and class status viz. convict, emancipated
convict, free settler, military, or government official. Both sons were named
and recognised as Laurence Butler’s sons in his Will of 1820. So this further
confirms that Laurence Butler Senior was undoubtedly the biological father of
Walter and Lawrence Junior.
'Familytreedna' interprets the criteria for Genetic Distance at 67
Y-Chromosome STR markers, when two men share a surname:
A Genetic Distance of 3 or 4 are related- 63/67 or 64/67 match
between two men who share the same surname (or a variant) means that they are
likely to share a common ancestor within the genealogical time frame.
The common ancestor is probably not extremely recent but is likely within
the range of most well-established surname lineages in Western Europe.
The 'Genealogical Time Frame' is the most recent one to fifteen
generations.
'Recent genealogical times' are the last one to five generations.
A Genetic Distance of 1 or 2 are tightly related- 65/67 or 66/67
match between two men who share the same surname (or a variant) indicates a
close relationship (within one to five generations). It is most likely that
they matched 36/37 or 37/37 on a previous Y-DNA test. Very few people achieve
this close level of a match.
In the case of these two descendants, 7th
generation down from Laurence Butler is not classed as within the ‘recent
genealogical time-frame of 5 generations’, which accounts for one extra
marker variation, viz. 64 out of 67, in that time-frame. Notably, all three
marker changes were in fast changing STR’s (DYS570, DYS557 and DYS446).
The Y-DNA match plus the matching genealogy, proves beyond doubt
that Walter and Lawrence Junior were true blood brothers, and both sons of
Laurence Butler Senior.
In the Butler Surname Y-DNA Project, Atkins is
included with the two Butler descendants. The 1st Butler (444174-
IM253) is Lawrence Jnr's descendant, and the 2nd Butler (294887) is Walter's descendant. NB. Lawrence Jnr's descendant's haplogroup is designated I-M253 as he has not undertaken the Big-Y SNP test:
The Y-DNA tests therefore provide us with Laurence Butler's Y-DNA haplotype signature for 67 markers,
plus the probable haplotype for the remaining markers between 67 and 111 (with
the possibility of some further mutations occurring in one or two of
the remaining markers, noting that some markers are more prone to mutations
than others). Only an upgrade to a 111 marker test of the second descendant, or
of another descendant, would prove if there are any further mutations.
The testing of these two descendants of Laurence's two sons by two different women, is a rather rare and unusual scientific study, providing absolute proof of the Y chromosome haplotype of a man, born in 1750 living more than 260 years ago, and where the paper trail of descent matches the Y-DNA evidence.
After several generations of coexistence and intermarriage, a group of mixed Irish and Norse ethnic background arose, which shows in the DNA evidence in some residents of these coastal cities, particularly in Wexford, to this day.
'Recent genealogical times' are the last one to five generations.
Explanations:
DYS393 - 13
DYS390 - 23
DYS19 – 14 (also =DYS394)
DYS391 - 10
DYS385 - 13-14
DYS426 - 11
DYS388 - 14
DYS439 - 11
DYS389I - 12
DYS392 - 11
DYS389II - 28
Panel 2 (13-25)
DYS458 - 16
DYS459 - 8-9
DYS455 - 8
DYS454 - 11
DYS447 - 23
DYS437 - 16
DYS448 - 20
DYS449 - 28
DYS464 - 12-14-14-16
Panel 3 (26-37)
DYS460 - 10
Y-GATA-H4 - 10
YCAII - 19-21
DYS456 - 14
DYS607 - 14
DYS576 - 17
DYS570 – 19 (matches with Atkins)
CDY - 36-38
DYS442 - 12
DYS438 - 10
DYS531 - 11
DYS578 - 8
DYF395S1 - 15-15
DYS590 - 8
DYS537 - 11
DYS641 - 10
DYS472 - 8
DYF406S1 - 9
DYS511 - 10
Panel 4 (48-60)
DYS425 - 12
DYS413 – 24-24
DYS557 – 15 (matches with Atkins)
DYS594 - 10
DYS436 - 12
DYS490 - 12
DYS534 - 15
DYS450 - 8
DYS444 - 14
DYS481 - 25
DYS520 - 20
DYS446 – 13 (matches with Atkins)
Panel 4 (61-67)
DYS617 - 13
DYS568 - 11
DYS487 - 12
DYS572 - 11
DYS640 - 11
DYS492 - 12
DYS565 – 11
Theobald FitzWalter (1st Hereditary Chief Butler of Ireland appointed 1177)
Theobald FitzWalter d.1230 (2nd Hereditary Chief Butler of Ireland)
Theobald Butler d.1248 (3rd Hereditary Chief Butler of Ireland)
Theobald Butler d.1285 (4th Hereditary Chief Butler of Ireland)
Edmund Butler d.1321 (6th Hereditary Chief Butler of Ireland)
John Butler 1306- 1330 (brother of James 1st Earl of Ormond 7th Chief B)
Edmund Butler
Pierce Butler
James Butler
James Butler
Pierce Butler (?of Lismalin Tipp d.1526)
James Butler
James Butler
Sir James Butler of Lismalin Tipp.
Sir Pierce Butler d.1661(1st Viscount Ikerrin) m.Ellen Butler (d.o. Walter 11th E. of Ormond) d.1668 BTR8
James Butler (Hon) 1616-1638 BTR373) m.Ellen Butler (d.o. Edmund 3/13th Baron Dunboyne & Margaret Butler)
Pierce Butler 1637-1661 (2nd Viscount Ikerrin) m Eleanor Bryan in 1657
James Butler 1658- 1688 (3rd Viscount Ikerrin) m Eleanor Redman in 1678
Thomas Butler 1683- 1719 (Rev 6th Viscount Ikerrin) m Margaret Hamilton
Somerset Hamilton Butler 1718-1774 (8th Viscount Ikerrin and 1st Earl of Carrick in 1748) m.1745 Juliana Boyle d.o. 1st Earl of Shannon
Henry Thomas Butler b.1746 d.1813 (2nd Earl of Carrick) m.1774 Sarah Taylor
Henry Edward Butler b.1780 d.1856 (Lt Gen) m.1812 Jane Gowan (second son- when eldest brother 3rd EofC and 2 heirs died, Henry’s grandson inherited as 6th EofC)
Charles George Butler b.1823 d.1854 m.1850 Jane Elizabeth Prosser
Charles Henry Somerset Butler b.1851 d.1909 (6th Earl of Carrick) m.1856 Ellen Sarah Morgan
Charles Ernest Alfred French Somerset Butler b.1873 d.1931 (7th Earl of Carrick) m.1898 Ellen Rosamund Mary Lindsay
G.S.L. Butler b.1905 Dublin d.1983
R. L. S. Butler born New Zealand
CONCLUSION
Laurence Butler- what was he like as a man?
At his trial, Laurence claimed he was not politically involved in the United Irish movement before the rebellion, and was forced by the tide of revolution sweeping his county to become an active participant. His initial reaction to becoming involved, knowing full well the repercussions of failure, was to “hide under the bed” when his acquaintances came to fetch him. As he was accused of “disguising himself in women’s clothing and returning home” that same evening, it would suggest that he was rather horrified by the atrocities being committed by some of the more extreme rebels on Vinegar Hill. However, on reflection that night, he apparently returned voluntarily the following day and became actively involved in the struggle. As he was elected a captain of his unit, was mounted on a horse, and was eventually tried in a court-martial, he must have had some standing in his community. He "carried the colours” at the battle of Tubberneering, probably for his local parish unit of Ferns, which indicates a position of trust and respect. It possibly also indicates that his role was a non-combative one, probably due to his age and disposition. A further witness stated that he had heard that Laurence had been quite “active” during the uprising, so at some point, Laurence must have realised that there was no turning back, and that failure meant the loss of everything he had worked for throughout his life, as well as life itself. However, his defence may have also been a ruse to save his skin from the dire consequences of conviction, and he may well have played an active role in the United Irish Society well before the uprising began, as the society was very active in the region of Wexford in the near vicinity to where Laurence lived. The Orangemen Society led by local landowner in Ferns, Richard Donovan, was conducting secret meetings at the old castle in Ferns. That cannot have gone unnoticed by Laurence and may have fired up his support of the opposing United Irish Society. His true beliefs in this matter will remain a mystery. However, non-participation in any of the Irish disturbances or revolts in his years living in the Colony would suggest that he was not politically active.
In 1816, Laurence purchased the lease of his second Pitt Street property from his neighbour Samuel Terry, having previously bought the Kent street and Elizabeth street properties the year before. The Pitt Street purchase was of considerable value, having paid ₤400, and put him into substantial debt to Samuel Terry (considered the richest man in the colony). Although this appears to have caused a problem financially for a short period, evidenced by his court case with D'Arcy Wentworth, his financial situation at this time must have been very profitable, possibly largely due to his substantial Government furniture order for the new Courts of Law buildings.
In the same year, on the recommendation of D’Arcy Wentworth, he was granted 100 acres neighbouring Dr. William Balmain's grant, and Captain John Piper and Major George Johnston’s land grants. For Laurence to be granted land in an area reserved for community leaders and high ranking military officers, would indicate he had some standing and influence in the community. He must have had a close association with someone with influence, probably Wentworth, a fellow Irishman. He carefully nurtured a business rapport with the Protestant members of the community, as most of his clientele were English Protestants. This was also evidenced by his financial support of the Protestant Bible Society. Laurence was one of only four Irish businessmen and inhabitants of Sydney (including William Davis, Ed Redmond and Patrick Cullen) who were signatories to the 1817 Memorial to Governor Macquarie, signed by seventy-eight of , as Macquarie stated in his own words, ‘a great majority of the most respectable Inhabitants of the Colony’, requesting Macquarie to rescind a Government restriction on the importation of goods from England. To be included in this list shows his standing and acceptance in that community.
He also had considerable business skills, not only as a cabinet maker but also as a merchant. At various times he appeared to be in considerable debt which was due to expansion of the business and property investments, plus poor cash flow due to the difficult currency situation in the Colony. He was not averse to using the Civil Court system to sort out his monetary problems with customers and suppliers as evidenced by his stand against West and Laing, resulting in their disputes being sorted out in the Civil Court. Just as happens today, one had to be paid by customers before one could pay the suppliers, and the promissory note system hindered fast payments of debt. The lack of any banking system in the Colony must have greatly hindered progress.
There was also his friendship with Isaac Wood who arrived in 1813 from Wexford for a seven year sentence, and set up an educational Academy for young gentlemen. Both Hayes and Woods witnessed his Will.
Employee, Miles Leary, who had a relationship with Ann Roberts after Laurence’s death, was also from Wexford and was probably related to another Wexford rebel John Leary. The Learys came from the Gorey district, a few miles north-east of Ferns, and John and James Leary were transported on the 'Atlas 2' with Laurence.
His close friendships with rebels from Wexford in particular, does seem to indicate that he had lived there for a considerable time, and was maybe a native of Wexford.
trustworthiness, and strength of character who was a respected member of the fledgling community of Sydney. He left a legacy to his new country in the form of his beautiful furniture, which exists to the present day in museums and in private collections.
As an ancestor, he was a man to be proud of.
The Wearing of the Green
Contact email butler1802 @hotmail. com (NB. no spaces)
Link back to Introduction:
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-intro.html
Links to all the chapters in this blog:
The 1798 rebellion
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch1-1798-irish-rebellion.html
Laurence Butler's trial for his role in the Rebellion
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch2-butlers-trial_7.html
Analysis of Butler's trial
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-3-trial-analysis_7.html
Laurence Butler at the Battle of Tubberneering
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-4-battle-of-tubberneering.html
Laurence Butler's imprisonment
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-5-butlers-imprisonment.html
Butler's life and family in Wexford
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-6-family-and-life-in-wexford.html
Laurence Butler's transportation to Sydney in 1802 on the Atlas 2
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-7-transportation-to-sydney.html
Conditions on Convict Ships
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-8-conditions-on-convict-ships.html
Life as a convict in Sydney
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-9-life-as-convict-in.html
Laurence Butler's property investments in Pitt Street Sydney
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-10-butlers-property.html
Sydney Town in 1800-1810
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-11-sydney-town.html
Laurence Butler's petitions to the Governor
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-12-butlers-petitions.html
Laurence Butler's 100 acre land grant in District of Petersham
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-13-butlers-land-grant.html
Butler's membership of the Commercial Society of Sydney
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-14-commercial-society-of-sydney.html
Laurence Butler's court cases
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-15-court-cases.html
Laurence Butler's business interests in Sydney
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-16-butlers-business.html
Laurence Butler's cabinet making business
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-17-cabinetmaking.html
Laurence Butler's property investments in Sydney
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-18-property-investments.html
Laurence Butler's colonial family
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-19-butlers-colonial-family.html
Laurence Butler's death in 1820
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-20-butlers-death.html
Laurence Butler's issue- Walter, Lawrence Junior and Mary Ann
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-21-butlers-children.html
The Catholic Community of Sydney up until 1820
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-22-catholic-community-sydney.html
Genealogy- Butler's possible ancestry and possible descendants in Ireland, and BDM records
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-23-possible-birth.html
Butler's fellow Irish rebels transported to Sydney
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-24-rebels_12.html
Conclusion about the life of Laurence Butler
http://butlerfamilyhistoryaustralia.blogspot.com.au/2012/08/laurence-butler-ch-25-conclusion.html