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;aturday, January 8, 2000 Statement.

Subject: Statement.
Date: Fri, 24 Dec 1999 12:44:05 -0400
From: "BaiTY & Barb G.llptill" .1: b.ca>
To: Clmc"ka Jet obI "t.ub.cd>
Hi folks, Here is a copy of the statement my f<lther prepared and had notarized a month or so ago. If you want to
send me a fax number, I can fax the notarized item to you. Regards, Barry Guptill.
************************************************************
The following is a true statement as 1 remember it and as I know it to be.
My grandfather, Sidney Nason Guptill, (1873 to 1956) was in appearance and disposition an Indian. He lived with my
father's (Ralph Weston Bancroft Guptill, 1902 to 1971) family from before my birth in 1924, until his death, with the
exceptions of a few short breaks for employment off Grand Manan Island. As a child, a boy & a teenager, I spent
much time in the woods with him. He knew the names of all the different birds & flowers, & never tired of naming &
talking of them. He used roots, leaves & other thjngs as medicine and especially of a tree that he called Balm Gilead.
As a child, we had no TV or radio, so he spent many hours telling my sister Bernice Guptill Thomas and I stories &
showing us pictures in his very large picture album----. He had a picture of a lady who was very obvious an Indian &
in showing us her picture he would always say" This was my Grandmother. She was a full blood Mic-Mac lady, and
she was a lady." In one of the pictures she was smoking a clay pipe and I feel that was why he always added H and she
was a lady." Her name was Elizabeth Tomah (or possibly Thomah) Thomas Cheney (1818 to 1911) married to
William Guptill.
He never explained the Cheney that I remember, but it was obvious where the Thomas came from. Tomah (or
Thomah) was not a middle name, but her Maiden name.
My father Ralph & his two brothers Denison Percy (1894 to 1956) & Vance RUpelt (1899 to 1959) knew great
Grandmother & accepted the fact that she was an Indian Lady & never seemed to be ashamed of her, but some cousins
were. Denison's grand children look very much Indian & some of them live in Labrador & are married into local
Indian families. Grandfather Sidney's brother, Judson Jr. had the Indian look & many of his children & grandchildren
were Indian in appearence. His sister, Susan Guptill Wooster, as I remember her in her rocking chair with a shawl
around her shoulders, looked very much like Old Grandmother Tomah.
I have no doubt of my Indian ancestry & I am very proud of it. The album and pictures of Grandmother Tomah have
long since disappeared or are hidden by some family member, as some were ashamed of Old Grandfather William
marrying an Indian.
Signed, sworn to, witnessed and sealed in New Brunswick,
this day of 1999.
Signature: Witness: _
Keith Bonden Guptill.
mailbox:/SuperMac%AA%20HD/System%20FoJdffl
Preferences/Netscape%2OUserslArt%20MacKayI
Subject: New II cousins"
Date: Fri, 05 Mar 1999 19:3313 +0000
From; ART ]vIACKAY <2ll1ackav@nbnetnbca>
ART MACKL\Y STUDIOS
To; "Kosky, Kem
'
Guptill" <wal tel'. j .koskv@snet.net>
'-.-.
BCC: kpenlton@nbnet.nb.ca
Hi Kerry:
Thanks for the e-mail and the information. I am just beginning to try
and piece together my families. My references up to now have been the
Grand Manan Historian, primarily XVII "Family History" which reprints
the Census of 1851, but other issues as well. Also there are a number of
other local references which are Interesting and useful. In any event
my "connection" follows:
abt 1650 Thomas Gubtail
married
Mary Abbott
begat
1685 Nathaniel Gubtail
married
Mary Isselton
begat
1726 JOM Gubt3il
married
Abigail Goodwin
begat
1756 \M.lliam Gubtail
married
Jane Downs
begat
17'70 \Nilliam Gubtail
L ed
Mar)1 Ann Smith
begat
1814 \Mlliam Gubtail
married
Bizabeth Cheney*
begat
Judson L Guptill (Sr)
married
Susan Bancroft**
begat
Judson L Guptill Or)
married
Caroline Foster
begat
Chester L Guptill
married
Eula M. Russel
begat
Lois Muriel Guptill ***
married
,",Vesley Stew811 McKay (MacKay)
begat
Ar1hur Allison McKay (MacKay)
married
Margaret Rose Getchell ****
begat
K Allison

Clifford Penclleton* ** **
*Bizabeth Thomas Cheney - mystery lady #1. There appears to be no
record of Bizabeth being from other Cheney families on Grand Manall.
However, I ran across a reference to her coming from Indian Island, an
important trading post close to Deer Island, Campobello and Eastport
T ~ c o r d s include her siblings but I cannot find the names of her
pc.......dts. I am seeking more information on her family
** Susan (Susanne Bancroft) - mystef'j lady #2 - The census of 1851 lists
her as being a "Lodger" at William's home (18 years of age). Judson L
was 15 years at this time. They later married. Susan also is not listed
as a member of other Grand Ivlanan Bancroft families. One note suggests
she came from Machias. Others suggest that she came from Nova Scoria. I
am seeking information on Susan as well
*** Lois Muriel (Guptill) McKay is my mother. She is 89 this spring and
as bright as can be. She was delighted when I told her about your web
site and the information on it. Our family myth "vas that the Gubtails
were Dutch!!! She thought that she liked the idea of Wales nevertheless I
She has requested printed copies which I am to deliver forthwith!
****Margaret Rose Getchell As a matter of interest, Marg's family came
from one of the first settlers at St. Stephen, N.B. He moved from
Machias and the connections and moves are very similar to those of the
Gubtail's. Interesting history ... one of her relatives was the guide
for Benedict Amold when he went up the Kennebec to attack Quebec in
1775.
***** Kimberly (MacKay) Pendleton, I noticed the reference to the
numerous marriages between the Gubtails and Pendletons ... the tradition
continues!!! !
Please feel free to add me to your "cousin chart". Yes I would love to
re
r
'Ie a
cc I think that I might have some Grand 1vlanan infonnation which would
interest you. Unfortunately, I haven't had time to digitize it. I would
be glad to fa.x or mail copies of what I have if you would like. My
brother has tons of material which I am trying to get access to and I
hope to gradually get it all together sometime.
Thanks for \'vriting. I hope that this is all of interest to you.
Kind Regards
Art MacKay
amackay <amackay@nbnetnb.ca>
Art lvfacKay Studios
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What 1S DNA and Genealogy
All humans have 23 pairs of chromosomes, including a pair of sex chromosomes, known as "X" and "Y".
Males have both an X- and a Y-chromosome (with the Y-chromosome inherited from the father) while
females have two X-chromosomes (one X-chromosome inherited from each parent.) Genetic Genealogy
is interested in heritage markers or the area of the chromosome which reveals family relatedness.
Father-to-Son
Because the Y-chromosome is passed essentially unchanged from father-to-son, it provides genetic
genealogists with a powerful tool for tracing a paternal lineage. Specific portions of the Y-chromosome
are analyzed and compared against other partidpants' Y results to determine the relatedness between
the two participants.
Mother-to-Child
Since both parents contribute X-chromosomes to their daughters, a different source of DNA must be used
to trace the maternal line. Mitochondrial DNA (mtDNA) is inherited by both male and female children
exclUsively from their mothers and provides insight into one's maternal lineage. (!,-earn m re about
mitochondrial D ~ c )
What DNA Ancestry Testing Cannot Do
The type of testing performed by DNA Ancestry is limited to areas of DNA that have the greatest
application to genealogy which reveal insight into family relatedness. The portion of DNA tested is within
the non-coding regions and do not prOVide distinguishing information about an individual such as hair
color.
While DNA testing in general has a promising future as a tool for predicting one's chances for developing
disease such as diabetes, Alzheimer's, and cancer; DNA Ancestry does not perform medical diagnostic
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A common application of DNA testing is in determining the paternity of a child for custody or inheritance.
Results of a DNA Ancestry test can definitively disprove a genetic relation. A large number of mismatches
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other hand, cannot be used as legal proof of paternity, but can serve as a strong indication.
Privacy
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hides your Ancestry .com username, but allows your DNA results to still be matched with others in the
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genetic cousins and, if the match is close enough, contact them safely and anonymously.
Connection Service
Your privacy is also protected by using Ancestry.com's Connection Service to contact other DNA
participants. The Connection Service allows you to send an e-mail to a potential genetic relative without
revealing your own e-mail address. Instead, the message is sent through Ancestry .com and the system
transfers the message to your e-mail address without revealing your actual address. Replies can also be
made through the Connection Service until you feel you wish to make direct e-mail contact with the other
party.
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How do I collect a sample?
Collecting a DNA sample is easy and painless. Simply swab the inside of your mouth to collect cheek cells
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Shortly after you confirm your order, you'll receive an e-mail indicating that your test kit has been sent.
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Step 1 - Prepare to Collect DNA Sample
Included in each DNA Collection Kit, is a form printed on the Collection Envelope to be completed by the
participant (person prOViding the DNA sample.)
Before you collect the sample, make sure you have waited at least 30 minutes from your last meal or
snack to help reduce sample contamination.
Step 2 - Collect DNA Sample
Open the Swab Packet and remove one swab. Leave the other swabs in the sterile package until
ready for use.
Holding only the stick portion (do not touch the swab area), rub the swab up and down the inside
left wall of your mouth. Vigorously scrape the inner left cheek using a vertical, up-and-down
motion. Rotate the swab while scraping the inner cheek surface. Do this for a minimum of 30
seconds.
Place swab directly into the Collection Envelope. Do NOT put it back into the Swab Packet. Do NOT
touch the swab area to any other surface.
Repeat steps A and B with the remaining two swabs in the Swab Packet, swabbing the inner right
cheek with one of the swabs and the inside front of the mouth with the other.
This kit is for one individual only. The same person must use all three swabs.
Do NOT return samples from more than one person in a single envelope.
We recommend leaving the Collection Envelope open for about 30 minutes after collection to allow
the samples to dry before sealing the envelope.
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Once the swabs have dried, carefully place them into the Collection Envelope and enclose this envelope
into the pre-addressed mailing envelope. If you are mailing from outside of the United States or Canada,
please place the appropriate postage on the envelope.
You will receive an e-mail notification when the lab receives your DNA sample, and again when your DNA
results are available. It only takes a few weeks for the lab to process your DNA and make your results
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Once your test results have been entered into the system, DNA Ancestry will continually look for people
who have similar DNA results so that you might find your long lost genetic cousin.
The Science Behind Genetic Genealogy
The follOWing sections prOVide an overview of the science behind DNA and genealogy. It will familiarize
you with some of the technical terms commonly used in the field of genetic genealogy.
DNA is found in every cell in your body except the red blood cell. It is located in the center of the cell in a
membrane called the nucleus. DNA contains all the information necessary to coordinate the functions of
your body from wiggling your toes to operating your heart. That's a lot of information! A typical animal
cell contains one meter of DNA. Written in a linear alphabet of four letters, the genetic information carried
in a human cell could fill a book of more than 500,000 pages' But how is that much information packaged?
DNA is tightly wrapped in configurations known as Genes, which are the functional units of DNA. Genes
prOVide provide the instructions for life. The human genome is estimated to contain 30,000 to 40,000
genes.
Only about 2% of the human genome contains genes; the remainder consists of non-coding regions,
whose functions vary from proViding structure to the chromosome, to having no detectable purpose. It is
these non-coding segments that are being compared for genealogical purposes.
Humans have a total of 46 chromosomes, which are grouped into pairs. Each of the 23 pairs consists of
one chromosome from our mother and one from our father. In females the 23rd chromosome pair
consists of two X-chromosomes. Males, however, have an X-chromosome and a V-chromosome. It is,
therefore, the V-chromosome (Yes) that determines the male gender. It is also the V-chromosome (Yes)
that is one of the most useful chromosomes in genealogical studies. The Y-chromosome has the unique
property of being passed virtually unchanged from generation to generation. This means that a man and
all his sons will have the same, or similar, V-chromosome. likeWise, he will have the same
V-chromosome as his father and grandfather and so on. This gives the V-chromosome the unique
property of following the surname, in most cases, which makes it a very valuable genealogical tool.
In addition to DNA found within the nucleus of the cell, DNA can also be found in the mitochondria of the
cell. The mitochondria is the power house of the cell. It is responsible for producing energy to perform all
the cellular functions. The mitochondrial DNA (mtDNA) follows the direct maternal line. Women pass their
mtDNA to all of their children, but then only the daughters will pass it on to the next generation.
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:Jenetic Genealogy - Ancestry.com ...
>
DNA itself is a helical structure, similar to a ladder. The outside of the ladder is a sugar-phosphate
backbone and the rungs are made of paired nitrogenous bases. These bases come in four varieties:
Adenine (A). Thiamine (T), Cytosine (C), and Guanine (G). A always pairs with T and C always pairs with
G along the rungs of the ladder.
The type of testing performed by DNA Ancestry is limited to areas of DNA that have the greatest
application to genealogy which reveal insight into family relatedness. Heritage markers are within the
non-coding regions and do not provide distinguishing information about an individual such as hair color.
Typically there are three main kinds of analysis performed for genealogical purposes: DNA sequencing,
Single Nucleotide Polymorphism testing (SNPs), and Short Tandem Repeat testing (STRs).
DNA Sequencing is the process of determining the exact base pair sequence in a predetermined section of
DNA. This technique is most often used in mitochondrial DNA (mtDNA) testing where the sequence of
hypervariable region I (HVR I) and hypervariable region II (HVR II) is determined. This kind of analysis is
useful for direct maternal lineage testing or for maternal ancient ancestry typing.
Single Nucleotide Polymorphisms (SNPs, pronounced "snips") are single base pair changes that occur
infrequently throughout the genome. SNP testing is available for mtDNA, and V-chromosome. This testing
can confirm an indiVidual's deep ancestral grouping or haplogroup. While not directly genealogically
(recent past) relevant, haplogroups are instead anthropological (ancient past) in nature. This type of
analysis allows us to track the branching of haplogroups and subgroups from our original African home
and discover interesting facts about our own ancient ancestor's movements across time and geography.
Short Tandem Repeats (STRs) are segments of DNA that repeat themselves, for example a GATA
sequence repeated several times (GATA GATA GATA). Every individual has STR segments at specific
locations on the chromosome. The specific locations are referred to as Loci or Markers and are generally
noted as DYS###, for example DYS459. DYS indicates the location is on the V-chromosome at position
459.
While everyone has these repeated regions, the distinction between one individual and another is the
number of times the segment repeats. For example, at a given locus or marker on the chromosome, one
individual may have 12 GATA's, and another indiVidual may have only 10 GATA's. These numbers, 12 and
10, are called alleles. It is the collection of alleles for an indiVidual at specific locations (loci) that make up
his or her unique DNA profile or haplotype. These profiles or haplotypes are used for identification
purposes, to determine paternity, or to establish relatedness.
Ancient Ancestry - Haptogroups
About Haplogroups
Humans began to diversify as they migrated out of Africa and populated the rest of the world, adapting to
new climates, diets, and liVing conditions. Over tens of thousands of years, these ancient populations
became isolated and their DNA changed until they became genetically distinct from one another. These
deep ancestral groupings are referred to today as MPL9.C-Ql!.P5. Through DNA testing, we can track the
branching of haplogroups and their SUbgroups from the original African home and thus discover interesting
facts about our own ancient ancestors' movements across time and geography. DNA Ancestry prOVides a
complimentary haplogroup prediction with each V-chromosome or mtDNA test.
Paternal Ancient Ancestry
Your Ychromosome haplogroup can provide an interesting glimpse into the deep ancestry of your
paternal line. Every race of people indigenous to this earth is a member of a particular haplogroup. Your
Paternal Ancient Ancestry (or Haplogroup) is predicted based on your Y-DNA results. You will receive the
name of the haplogroup, a detailed description of the group, and a map showing how your ancient
ancestors migrated out of Africa over 100,000 years ago and split off to populate the different regions of
the world.
Approximately 18 major paterna/line haplogroups exist, known as A through R and are subdivided into
subclades represented by numbers and subsequent subclades labeled with a lower case alphabetic
character, e.g. E, E3, E3a. Haplogroup R1b is the most common haplogroup in European populations. It is
believed to have expanded throughout Europe 10-12 thousand years ago.
Major V-chromosome Haplogroups include:
Rib
I
B
E3a
E3b
J
Maternal Ancient Ancestry
Maternal ancient lineages or haplogroups can be subdivided into sub-lineages which are often regionally
or population specific. For example, haplogroup H accounts for about 50% of European populations. It is
believed to have originated in the Near East approximately 23,000-28,000 years ago and expanded into
Europe about 20,000 years ago. DNA Ancestry examines multiple regions of the mitochondrial DNA to
provide the most information possble about a maternal lineage. Participants can be either male or
female.
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