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Introduction and Summary |
D*mond
in
Colonial North America |
yDNA
All you need to know |
Contact Participate |
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Q-M3 Lineage |
Records |
I-M253 European Rooted Diamond, Dymond, Dimond Lineage
updated:
11.17.11
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Note to Participants
11.11.2011
1.
Please keep your personal pages at FTDNA updated and maintained.
Contact information etc.
2. Be aware that you can control match notifications. Multiple notifications can be irksome. I suggest adjusting the setting so that you are only notified of 37 marker matches. There is no good reason for 12 and 25. If you need help contact us. We can do it for you. 3. Visit your personal pages periodically. Personal pages at FTDNA have evolved over the past decade. There are more changes coming in 2012. Among these will be an association with Archives.com 4. Be aware you can add a ged. file to your personal page if you wish. This links your yDNA results with your family genealogy. 5. The page you are currently viewing is the primary location and home of the project. While I maintain the project page at FTDNA this is the page to come to for the latest and most complete information. Check this page periodically for new and updates. This is the primary source of communication. I will not personally email updates to each participant. If I do email you I will clearly indicate the reason in the subject line. 6. If you have any questions don't hesitate to contact us. There have been significant changes in the past couple of years.
Results pending:
All lines should be tested to a minimum of 37 markers.
The introduction of yDNA technology as a tool in 2002
led to the yDNA study of the D*mon(d) surname in
colonial America. That goal was met
in
2007. That same year Y chromosome testing of men believed to descend
from
Edward Dimond of Beekman Patent
thru his sons Johannes 1723, Marcus 1726, and Jabok
[Jacob] reveled two distinct biologic y lines. The
identified lineages are
Q-M3 or I-M253 rooted. Up until this time it was
believed that the Q-M3 lineage were descended from
Johannes and Jabok documented sons of Edward Dimond
though there has never been direct documentation that supports the
idea.
This conflict has not been resolved by either
traditional research or genetic testing. It remains
solvable by either means. |
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Genetic
Root [Deep] Ancestry The Single Nucleotide Polymorphism (SNP) M253 is a subclade within haplogroup I. Y DNA haplogroup I represents nearly one-fifth of the male population of Europe. It is found in the majority of present-day European populations; the greatest density is found in Bosnia and Herzegovina, Croatia, Norway, Sweden, Serbia, Sardinia, Denmark and Germany. The haplogroup is almost non-existent outside of Europe, suggesting that it arose here.
It is believed that generations of Dimonds from both
Kittery and Marblehead were involved in the seasonal
fishery at Newfoundland, sometimes manning their own
schooners. The Maritime History Archive at St. John’s,
Newfoundland, is a repository for a number of records on
the merchants and ship owners of New England and their
dealings with the fishermen. The fact that such records
are housed in St. John’s speaks to the relationship
between the two colonies. For example, in the fishing
account books (1658-1672) of George Curwen, a prominent
Salem merchant who supplied fishermen at Salem and
Marblehead, there is a record of Edward Diamond (of
Marblehead), whom he outfitted in 16631,
providing him with such sundries as soup plates,
stockings, “woolmill mittings”, salt, gloves, hooks, and
a knife. A century later, William and Benjamin Knight,
shoremen from Marblehead who were themselves involved in
the deep sea cod fishery, similarly outfitted Joseph
Diman of Salem (1756), Jeames (sic) Dimon of Gloucester
(1759), and John Diamont of Danvers (1773).
Documentation for this time
is scarce, but from piecing together what is available
it appears that William arrived with what must have been
his parents and at least two of his brothers. Old
cemetery records show that a John Dimond died in Adam’s
Cove in 1779 (six years after William staked his claim),
at the age of 56. Some 15 years onward, an Ann Dimond
and her son Robert were mortgaging property, including
their fishing room or plantation, in Adam’s Cove.4
This property bordered on the land claimed by William
Diamond in 1773. Two years later, in 1796, this property
formed part of the holdings of William Dimond & Co.—at
that time the property was, the claim stated,
“bequeathed by mother’s Will”. This suggests that Ann,
who was clearly the owner of the property in 1794, had
died sometime between 1794 and 1796. It therefore seems
reasonable to infer that:
It is not surprising that
John Sr.—or Ann, for that matter—does not appear in
these early property records: These records were created
in 1805, and although any claims of ownership were
back-dated, the records reflected only those owners
alive in 1805.
Lower Island Cove
John stayed, and with his
wife, Grace Snelgrove (c 1787-1883), raised a large
family, consisting of at least two daughters—Ann (abt
1831) and Eliza (1833)—and five sons: twins Peter
(1817-1874) and James (1817-1887), William (bef 1827),
Robert (1827), and Nathan (1836). In later years, around
1852, Peter, James, and Nathan would move to Russell’s
Cove (now known as New Melbourne), while it would appear
that William and Robert would eventually (after 1871)
move on to St. John’s. There have been no Diamonds in
Lower Island Cove since at least the 1890s and probably
even before then.
Newfoundland
Peter Dimond abt. 1790 - 1864
Clement Diamond 1840
Locations: Adam’s Cove Lower Island Cove Russell’s Cove (now New Melbourne) Flat Islands (later called Port Elizabeth Participant Lines: Lower Island Cove
197085
Adams Cove
211892
GB20026
New York Branch The majority of these sons were over twenty year of age during the Revolution. They must be taken into account when attributing records.
Locations:
New York Branch
Link to Stephentown Genealogy
Possible descendants of Marcus1726
and Edward Dimond
of Beekman and Kinderhook
New York Province and in turn may be descendants of Edward
Dimond of Marblehead Massachusetts Colony
119366
Edward1 Dimond, b. c 1695, NY Colony m. Christina Snyder Marcus2 Dymond, b. 1726, NY m. Marytje Simson John3 Dymond, b. m. Elizabeth Peter4 Dymond, b. , m. Lucretia Amidon Charles5 Dymond, b. , m. Sarah Ann Robinson
George6
Dymond, b. , m. Lydia Cleveland
Floyd James7 Dymond, b. , m. Mota L. McKinney Pvt8 Pvt9
43806
Edward1 Dimond, b. c 1695, NY Colony m. Christina Snyder Marcus2 Dymond, b. 1726, NY m. Marytje Simson John, Abram, or Henry3 Dymond John4 Dymond, b. 1809, m. Avis Simkins George5 Dymond, b. 1828, m. Betsey Pratt
William6
Dymond, b. 1865
Ulysses7 Dymond (Sweener) , b. 1899 Pvt8
128052
Edward1
Dimond, b. c 1695, NY Colony
m. Christina Snyder
Marcus2 Dymond, b. 1726, NY m. Marytje Simson John, Abram, or Henry3 Dymond John4 Dymond, b. 1809, m. Avis Simkins George5 Dymond, b. 1828, m. Betsey Pratt
George6
Dymond, b. 1856, m.
(1)
Abba
(2)
Laura M.
George7 Dymond , b. 1894, m. Sarah L. Pvt8 Pvt9
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Y Haplotype Signature A 67 marker yDNA modal haplotype has been identified [subject to change] . A deduced ancestral haplotype [subject to change] to about 29 makers represents the haplotype of the oldest common ancestor.
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Descendant
Lineage Chart
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Haplotype Data
Note that there are random mutations away from
the modal and ancestral. These are expected in
two hundred and fifty years (5 to 7
generations). Mutations ‘Altered DNA’ is another name for mutation. In molecular biology and genetics, mutations are changes in a genomic sequence: the DNA sequence of a cell's genome or the DNA. They can be defined as sudden and spontaneous changes in the cell. Mutations are caused by radiation, viruses, transposons and mutagenic chemicals, as well as errors that occur during meiosis. No one has yet established a connection between any mutagenic agent and the particular kind of mutation we measure replication slippage in STRs [Short Tandem Repeats] which is simply the lack of absolute perfection in counting repeats in the Y chromosome. The mutations we are measuring occur during the continuous process of sperm creation through replication slippage. At the point in time when sperm reside "in" the father most of the millions of sperm in an ejaculate will be identical for the markers we test, but a extremely small fraction will differ. The occurrence of a mutation in a son is therefore a matter of chance as to which sperm fertilizes the egg. When we say the mutation occurred "in" the son, that's saying the mutation occurred during the creation of the sperm that fertilized the egg that developed into the son. The next son to be born is a product of the same process, and his haplotype is independent of the prior son or future sons. The father's DNA has not changed. The next ejaculate will be similar, with sperm that are identical for the most part but with a few mutations occurring in a random fashion. Genetic genealogy Paternal line genetic genealogy studies the sequences of repeating nucleotide (the base components of DNA) patterns on the Y chromosome known as short tandem repeats (STRs). Each STR is considered a separate marker for potential genetic matching because the number of times it is repeated will be the same for related males.
If a father were to have sons, no matter the number, the
odds are extremely high that all will have the same yDNA
measurements as their father. Every so often there will
be the rare random mutation. This son will have a
measurement that is different than his brothers and
father. We can use this knowledge to study and construct paternal lineage relationships Process The first and primary use of Y DNA is to prove or disprove relationship to a specific paternal lineage. This can be taken a step further by assembling lineage descendant haplotype data across as many descendants of a common paternal ancestor as possible. The first step is to first determine the modal lineage haplotype. Modals are determined by comparing measurements marker by marker the greatest tally being the modal. As sample size increases we begin to see within the charted data random mutations becoming branch defining mutations. Random mutations are today yet to be triangulated branch markers or are future branches. With each mutation sons and direct line male descendants beyond the man will there ever after carry the same mutation. It will become a branch defining marker. Through a carefully thought out process of testing appropriate brothers, cousins, and fathers is possible to triangulate to the individual where the mutation first occurred. With a broad representation of data across branches we can sometimes deduce the most distant common ancestor’s haplotype, this deduced ancestral haplotype. Many markers ancestral markers will mirror the modal haplotype and are obvious. Where there are branch markers this is not as cut and dried. Sample bias be a real problem
By working back from the modal or ancestral haplotype we
can, given enough data, construct a biological tree of
descent. This is especially important when considering
pre 1850 tree and branch constructions for accuracy
the paucity of documentary evidence obscures or
confuses.
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What is the data telling us? There are too few participants to determine the ancestral haplotype. Additionally data from Genebase and Ancestry is incomplete for comparison purposes however we can say we have firmly established the Y DNA signature of this paternal lineage. The lineage consists of two primary branches descending from a common ancestor. These branches separated some 300 years ago and have had no contact or knowledge of the other over this time. One branch settled in Newfoundland and the other in Massachusetts and New York. The Newfoundland branch in settled at least the 1700s and the Massachusetts and New York branch perhaps as early as the mid 1600s and certainly by the early 1700s. It is now proven that the Diamond's of Newfoundland all descend from the same common ancestor. This fact had been lost over time.
Markers
389-2, 449, 570, and 531 are random mutations
[un-triangulated branches]. Marker 449 is a clear
branch marker among the Newfoundland branch. |
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Genetic genealogy studies the sequences of repeating nucleotide (the base components of DNA) patterns on the Y chromosome known as short tandem repeats (STRs). Each STR is considered a separate marker for potential genetic matching because the number of times it is repeated will be the same for related males.
The true
nature of relationship in the earliest generations of the
Hudson's River Lineages and their branches are obscured by the paucity
of documents
pre 1800. The immediate benefit using the tool of yDNA technology along with traditional documentation has led to more accurate lineage constructions. |
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I-M253 Lineage Data |
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 | 21 | 22 | 23 | 24 | 25 | 26 | 27 | 28 | 29 | 30 | 31 | 32 | 33 | 34 | 35 | 36 | 37 | 38 | 39 | 40 | 41 | 42 | 43 | 44 | 45 | 46 | 47 | 48 | 49 | 50 | 51 | 52 | 53 | 54 | 55 | 56 | 57 | 58 | 59 | 60 | 61 | 62 | 63 | 64 | 65 | 66 | 67 | 68 | 69 | 70 | 71 | 72 | 73 | 74 | 75 | 76 | 77 | 78 | 79 | 80 | 81 | 82 | 83 | 84 | 85 | 86 | 87 | 88 | 89 | 90 | 91 | 92 | 93 | 94 | 95 | 96 | 97 | 98 | 99 | 100 | 101 | 102 | 103 | 104 | 105 | |||||||||||||||||||||
| 67 marker+
y haplotype Any male that is related in a direct line from the oldest common ancestor of the lineage will match or nearly match the ancestral haplotype Markers reported by Sorenson have been converted to FTDNA standard. These include: (441 [-1]), (442[-5]), (463[-2]), (H4[-11]), (A10[-2]) |
STR |
3 9 3 |
3 9 0 |
1 9 |
3 9 1 |
3 8 5 a |
3 8 5 b |
4 2 6 |
3 8 8 |
4 3 9 |
3 8 9 - 1 |
3 9 2 |
3 8 9 - 2 |
4 5 8 |
4 5 9 a |
4 5 9 b |
4 5 5 |
4 5 4 |
4 4 7 |
4 3 7 |
4 4 8 |
4 4 9 |
4 6 4 a |
4 6 4 b |
4 6 4 c |
4 6 4 d |
4 6 0 |
G A T A H 4 |
Y C A II a |
Y C A II b |
4 5 6 |
6 0 7 |
5 7 6 |
5 7 0 |
C D Y a |
C D Y b |
4 4 2 |
4 3 8 |
5 3 1 |
5 7 8 |
3 9 5 S 1 |
3 9 5 S 2 |
5 9 0 |
5 3 7 |
6 4 1 |
4 7 2 |
4 0 6 S 1 |
5 1 1 |
4 2 5 |
4 1 3 A |
4 1 3 B |
5 5 7 |
5 9 4 |
4 3 6 |
4 9 0 |
5 3 4 |
4 5 0 |
4 4 4 |
4 8 1 |
5 2 0 |
4 4 6 |
6 1 7 |
5 6 8 |
4 8 7 |
5 7 2 |
6 4 0 |
4 9 2 |
5 6 5 |
5 8 8 |
5 2 7 |
5 2 7 |
5 2 2 |
4 8 4 |
4 6 8 |
4 5 3 |
4 4 1 |
4 4 5 |
4 5 2 |
4 6 1 |
4 6 2 |
4 6 3 |
G A T A B 0 7 |
G A T A A 1 0 |
6 3 5 |
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# | SNP | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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John Diamond 1788 Lower Island Cove, Newfoundland |
John Diamond, James, John, Fredrick William , Pvt, Pvt | 197085 | I-M253+ | 13 | 22 | 15 | 10 | 13 | 14 | 11 | 14 | 11 | 12 | 11 | 28 | 15 | 8 | 9 | 8 | 11 | 23 | 16 | 20 | 29 | 12 | 14 | 15 | 16 | 10 | 10 | 19 | 21 | 14 | 14 | 16 | 21 | 35 | 35 | 12 | 10 | 11 | 8 | 15 | 15 | 8 | 11 | 10 | 8 | 9 | 9 | 12 | 20 | 21 | 15 | 11 | 12 | 12 | 16 | 8 | 13 | 25 | 20 | 13 | 13 | 11 | 12 | 11 | 11 | 12 | 11 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Peter
Dimond abt. 1790 Adams Cove, Newfoundland |
Peter Diamondabt. 1790, William Thomas Diamond1835, Joseph1858, Leonard1893, Pvt | 207266 | I-M253+ | 13 | 22 | 15 | 10 | 13 | 14 | 11 | 14 | 11 | 12 | 11 | 28 | 15 | 8 | 9 | 8 | 11 | 23 | 16 | 20 | 29 | 12 | 14 | 15 | 16 | 10 | 10 | 19 | 21 | 14 | 14 | 16 | 20 | 35 | 37 | 12 | 10 | 11 | 8 | 15 | 15 | 8 | 11 | 10 | 8 | 9 | 9 | 12 | 20 | 21 | 15 | 11 | 12 | 12 | 16 | 8 | 13 | 25 | 20 | 13 | 13 | 11 | 12 | 11 | 11 | 12 | 11 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Peter
Dimond abt. 1790 Adams Cove, Newfoundland |
Peter Dimondabt 1790, John Diamond1816, John Thomas Diamond1841, John Thomas1873, James Edison1909, Pvt, Pvt | 211892 | I-M253+ | 13 | 22 | 15 | 10 | 13 | 14 | 11 | 14 | 11 | 12 | 11 | 29 | 15 | 8 | 9 | 8 | 11 | 23 | 16 | 20 | 29 | 12 | 14 | 15 | 16 | 10 | 10 | 19 | 21 | 14 | 14 | 16 | 20 | 35 | 35 | 12 | 10 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Clement Diamond 1840 Adams Cove, Newfoundland |
Clement Diamond1840 | GB20026 | I-M253+ | 13 | 22 | 15 | 10 | 13 | 14 | - | 14 | - | 12 | - | 28 | 15 | 8 | 9 | 8 | 11 | 23 | 16 | 20 | 30 | 12 | 14 | 15 | 16 | 10 | 10 | 19 | 21 | 14 | - | - | - | - | - | 12 | - | 10 | 15 | 13 | 19 | 20 | 23 | 11 | 13 | 31 | 11 | 11 | 12 | 21 | 13 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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John Dymond 1809 Stephentown, NY |
Edward Dimond, Marcus1726 Dymond?, John , Peter, Charles, George, Floyd James, Pvt, Pvt | 119366 | I-M253+ | 13 | 22 | 15 | 10 | 13 | 14 | 11 | 14 | 11 | 12 | 11 | 28 | 15 | 8 | 9 | 8 | 11 | 23 | 16 | 20 | 30 | 12 | 14 | 15 | 16 | 10 | 10 | 19 | 21 | 14 | 14 | 16 | 20 | 35 | 35 | 12 | 10 | 11 | 8 | 15 | 15 | 8 | 11 | 10 | 8 | 9 | 9 | 12 | 20 | 21 | 15 | 11 | 12 | 12 | 16 | 8 | 13 | 25 | 20 | 13 | 13 | 11 | 12 | 11 | 11 | 12 | 11 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
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John
Dymond 1809 Stephentown, NY |
Edward Dimond, Marcus1726 Dymond?, John, George C., William C., Ulysses, Pvt | 43806 | I-M253+ | 13 | 22 | 15 | 10 | 13 | 14 | 11 | 14 | 11 | 12 | 11 | 28 | 15 | 8 | 9 | 8 | 11 | 23 | 16 | 20 | 30 | 12 | 14 | 15 | 16 | 10 | 10 | 19 | 21 | 14 | 14 | 16 | 20 | 35 | 35 | 12 | 10 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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John
Dymond 1809 Stephentown, NY |
Edward Dimond, Marcus1726 Dymond?, John , George C., George, George H., Pvt, Pvt | 128052 | I-M253+ | 13 | 22 | 15 | 10 | 13 | 14 | 11 | 14 | 11 | 12 | 11 | 28 | 15 | 8 | 9 | 8 | 11 | 23 | 16 | 20 | 30 | 12 | 14 | 15 | 16 | 10 | 10 | 19 | 21 | 14 | 14 | 16 | 20 | 35 | 35 | 12 | 10 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Dymond NY |
Genebase data - |
GB | I-M253 | 13 | 22 | 15 | 10 | 13 | 14 | - | 14 | - | 12 | - | - | - | - | - | - | - | 23 | 16 | 20 | - | - | - | - | - | 10 | 10 | 19 | 21 | - | - | - | - | - | - | 12 | - | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||