FA11

GEMS & GEMOLOGY
VOLUME XLVII
FALL 2011
FALL 2011
PAGES 181258
Pallasitic Peridot
Vietnamese Ruby and Sapphire
CVD Synthetic Diamond and
Synthetic Amethyst Identication
VOLUME 47
Diamond Stamp Collection
NO. 3
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GGWI10
Fall 2011
Volume 47, No. 3
EDITORIAL
181
New Beginnings
Jan Iverson
FEATURE ARTICLES
182
Carat Points
Ruby and Sapphire from the Tan HuongTruc Lau Area,

Yen Bai Province, Northern Vietnam
Nguyen Ngoc Khoi, Chakkaphan Sutthirat, Duong Anh Tuan, Nguyen Van Nam,
Nguyen Thi Minh Thuyet, and Nguy Tuyet Nhung
Although not as well known as the Luc Yen district, this area is an important
source of ruby and sapphire suitable for cabochons, including star ruby.
NOTES & NEW TECHNIQUES

pg.182
196
Infrared Spectroscopy of Natural vs. Synthetic Amethyst: An Update

Stefanos Karampelas, Emmanuel Fritsch, Triantafillia Zorba, and
Konstantinos M. Paraskevopoulos
High-resolution FTIR analysis can provide a conclusive determination of the
natural or synthetic origin of amethyst.
202
Exploring the Origin and Nature of Luminescent Regions in

CVD Synthetic Diamond
Bert Willems, Alexandre Tallaire, and Julien Barjon
Blue to blue-green luminescent zones, seen in the DiamondView instrument,
reveal the growth history of some CVD synthetic diamonds.
208
Identification of Extraterrestrial Peridot by Trace Elements

Andy H. Shen, John I. Koivula, and James E. Shigley
LA-ICP-MS analysis offers an excellent means of separating meteoritic peridot
from the earthly form.
214
A History of Diamonds through Philately: The Frank Friedman Collection

Stuart D. Overlin
Diamond history is chronicled in a collection of stamps and postal material.
pg. 218
REGULAR FEATURES
220
2011 Challenge Winners
222
Lab Notes
Large clinohumite Black diamond colored by plastic deformation Coated black diamond Pinkcoated diamond with natural spectroscopic features Untreated diamonds with high strain Subtle
HPHT color enhancement Luminescent cleavage Large HPHT-annealed pink CVD synthetic diamonds from Gemesis Treated pink synthetic diamonds Cultured pearls with plastic bead nuclei
Large conch pearl Be-diffused pink sapphire High Be in blue sapphires Green sapphires with
different chromophores
234
Gem News International

Greenish brown diamonds with color shift Afghanite from Afghanistan Ammonite from Madagascar Aquamarine from Vietnam Chalcedony from Peru Afghan emerald mining Fuchsite-rich
rock Color-change garnet from Tanzania Colorless gems from Myanmar Nuummite from Mauritania Blue opal from Mexico Freshwater cultured pearl beads Quartz with spessartine inclusions
Pink cats-eye quartz Rhodochrosite carving Sapphire and zircon from Ethiopia Sapphire mining in Sri Lanka Green cats-eye spodumene from Brazil Color-zoned topaz Variscite from Peru
Corundum and lead glass triplet Glass triplet resembling mystic topaz A jewel that survived 9/11
258
Book Reviews/Gemological Abstracts Online Listing
pg. 232
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THE
ABOUT
COVER
Pallasite is a stony iron meteorite that contains areas of gem olivine (peridot). In this issue, Dr. Andy H.
Shen and coauthors demonstrate the separation of pallasitic from terrestrial peridot by LA-ICP-MS analysis.
The pallasite slab is courtesy of Robert A. Haag (The MeteoriteMan, Tucson, Arizona). The 4.3-cm-tall peridot crystal from Myanmar is courtesy of William Larson (Palagems.com, Fallbrook, California). The 17.53 ct
trillion and the 20.25 ct square antique cushion, both from Pakistan, were faceted and supplied by Stephen
M. Avery (Colorado). The crystal and cut stones have been enlarged approximately 10% relative to the pallasite slab. Photo by Robert Weldon.
Color separations for Gems & Gemology are by Pacific Plus, Carlsbad, California.
Printing is by Allen Press, Lawrence, Kansas.
GIA World Headquarters The Robert Mouawad Campus 5345 Armada Drive Carlsbad, CA 92008 USA
2011 Gemological Institute of America All rights reserved. ISSN 0016-626X
NEW BEGINNINGS
hank you for t he warm welcome that I ve received as the new e ditor-in-chief of
Gems & Ge mology. I am pr ivileged to now be a par t of t he g emological community and to join such a passionate industryto be captivated not only by the beauty
of the gem world, but also by its science.
Of course, the challenge for scie ntists today is t he same a s it w as yesterday: to translate
ongoing research into definitive answers. As you k now, science do esnt a lways come u p
with absolutes; conclusions are mostly partial and incremental. Its like adding chapters to
a never-ending book.
We all know that technology is a lways pushing the
boundary of what is possible. Just look at its impact
not on ly on g em treatments, but a lso on m ining,
stone cutting , g em identification, and so on .
Gemologists now have to chase more subtle features in determining whether a g em is natural or
synthetic.
In this digital age, we can brace ou rselves or si mply
embrace the new wave of ( inevitable) change. As
the saying goes, change is constant. So the timeliness
and the fashion in which we disseminate scientific
results and i nformation will be more important
than ever to keep you abreast of these developments.
As I fol low in the footsteps of m y esteemed predecessors, this will continue to be a par t of G&Gs
mission, particularly as new g em and j ewelry markets open up and new challenges arise.
In this issue of G&G, we report on t he g eology and g emological characteristics of r uby
and sapphire from Yen Ba i Province, in nor thern V ietnam. There is an ar ticle by G IA
researchers on the use of trace-element analysis to distinguish meteoritic peridot from terrestrial p eridot, an d a
study of t he origin and
...the challenge for scientists today is t he same a s it
nature of lu minescent
was yesterday: to translate ongoing research into
regions in C VD-grown
synthetic diamond, which
definitive answers.
distinguish them from
natural material. We also
feature an important collection of diamond-themed stamps, and an update on the separation of natural versus synthetic amethyst using infrared spectroscopy.
I certainly look forward to working with all of you. Were not just in the industrywere all
a part of the industry as a whole.
I will close with Richard T. Liddicoats words from the Spring 1981 issue of G&G: It is the
intention of t he staff of Gems & G emology to provide g emologists and g em enthusiasts
everywhere with the latest developments and the most comprehensive coverage in the field.
This still rings true today!
Cheers,
Jan Iverson | Editor-in-Chief | jan.iverson@gia.edu
EDITORIAL
GEMS & GEMOLOGY
FALL 2011
181
RUBY AND SAPPHIRE FROM THE

TAN HUONGTRUC LAU AREA,
YEN BAI PROVINCE,
NORTHERN VIETNAM
Nguyen Ngoc Khoi, Chakkaphan Sutthirat, Duong Anh Tuan,
Nguyen Van Nam, Nguyen Thi Minh Thuyet, and Nguy Tuyet Nhung
Primary and secondary deposits in the Tan HuongTruc Lau area of northern Vietnams Yen Bai
Province have supplied rubies (especially star rubies) and some sapphiresmostly of cabochon
qualityfor more than a decade. The gems are typically translucent to semitransparent and pink
to purplish or brownish red, with rare color zoning. The most distinctive features of this corundum after polishing include growth zoning and asterism. The samples contain relatively high
amounts of Fe and variable Ti and Cr. The geologic origin and gemological properties of this
corundum are distinct from that of the adjacent Khoan ThongAn Phu area.
or more than 20 years, Vietnams Yen Bai

Province, and the Luc Yen District in particular,
have been widely known for producing highquality rubies and sapphires. Subsequent deposits
found elsewhere in Vietnam (Long et al., 2004)
include Quy ChauQuy Hop (Nghe An Province), Di
Linh (Lam Dong), Dak Ton (Dak Nong), and Ma Lam
and Da Ban (Binh Thuan). Still, Yen Bai remains the
countrys most important source of ruby and sapphire. Much of the production consists of cabochonquality stones from the Tan HuongTruc Lau area
(e.g., figure 1), as described in this article.
Vietnamese geologists first discovered gem-quality corundum and spinel at Luc Yen in 1983 (Vinh,
1991). In early 1987, the Geological Survey of
Vietnam found abundant gem material in alluvium
in Luc Yens Khoan Thong area. Mining activity
soon thrived, with many companies operating in the
region (Voi, 1991). Other gem occurrences near

Khoan Thong followed, such as Nuoc Ngap, Hin
Om, Khau Nghien, Vang Sao, May Thuong, May Ha,
An Phu, Phai Chap, Tan Lap, and Lam Dong. These
Figure 1. These star rubies (6.1611.66 ct) are from
the Tan HuongTruc Lau area of northern Vietnam.
Photo by Nuttapol Kitdee, GIA, Bangkok.
See end of article for About the Authors and Acknowledgments.

GEMS & GEMOLOGY, Vol. 47, No. 3, pp. 182195,
http://dx.doi.org/10.5741/GEMS.47.3.182.
2011 Gemological Institute of America
182
RUBY AND SAPPHIRE FROM NORTHERN VIETNAM
GEMS & GEMOLOGY
FALL 2011
H
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CORUNDUM DEPOSITS
Khoan Thong-An Phu area

arre
ea (old
(o mines)
Figure 2. In northern
Vietnams Yen Bai
Province, primary and
secondary corundum
deposits have been
mined on both sides of
the Chay River: the original Khoan ThongAn
Phu mines on the east
side and the newer Tan
HuongTruc Lau mines
on the west. The size of
each symbol is proportional to the importance
of that mining area.
Modified after Xuyen
(2000) and Vinh (2005).
25 km
Primary
Secondary
Tan
Huong-Truc
T
an Huong-T
ruc Lau area
arre
ea (new
(ne mines)
Primary
Secondary
Road
River or lake
Province
Pr
ovince boundary
District boundary
are located on the east side of the Chay River and

have been referred to by locals as bi cu , or old
mines (see figure 2).
In the mid-1990s, several bi mi (new mines)
were established on the west side of the Chay River.
These included Tan Huong, Truc Lau, kilometer 12
of National Road 70, Tan Dong, Hoa Cuong, Cam
An, Bao Ai, Ngoi Nhau, and Ngoi Hop (again, see figure 2). Although corundum was discovered in this
area in 1986 (Quan et al., 1998), there was no significant mining until local diggers arrived at Tan Huong
in 1994 (Thang, 1998). In 1996 the Vietnam National

Gold and Gem Corporation (VIGEGO) conducted
systematic assessments of Tan Huong (covering an
area of 6 km2) and Truc Lau (20 km2). Official mining operations by VIGEGO started at Tan Huong the
following year, yielding hundreds of kilograms of
ruby and star ruby (Thang, 1998). Subsequently,
other secondary (placer) and primary occurrences
were discovered and mined (e.g., Quan et al., 2000).
Currently, the only large-scale mechanized operation (figure 3) belongs to DOJI Gold & Gems Group
Figure 3. DOJI Gold &

Gems Group currently
conducts the only largescale mining activities
in the Tan HuongTruc
Lau area. These 2010
photos show open-pit
mining at Truc Lau (left)
and the associated processing plant (right).
Photos by N. N. Khoi.
GEMS & GEMOLOGY
FALL 2011
183
occurrences occupy the northeastern part of Yen Bai

Province, ~250 km northwest of Hanoi. From the
city of Yen Bai, it is easy to reach the new mining
area by driving northwest along National Road 70,
along which most of the occurrences are located.
This article describes the geology and gemological characteristics of gem corundum from Tan
HuongTruc Lau and compares it to the material
from the well-known Luc Yen deposits.
GEOLOGY AND OCCURRENCE
Figure 4. Local miners dig for spinel and corundum

at the Lang Chap occurrence in June 2010.
Photo by N. N. Khoi.
in the Truc Lau valley. Also some small-scale mining using primitive methods occurs sporadically,
particularly during the dry season. Most recently, in
February 2010, hundreds of local miners began operating illegally at Lang Chap, mostly for spinel (figure 4).
The mines on the west side of the Chay River
typically yield cabochon-quality ruby and pink sapphire. However, some very large rubies weighing
tens of kilograms have been found. Some of these
contain transparent, gem-quality portions that can
be faceted. A semitransparent to nearly transparent
290 ct fragment, detached from a 2.58 kg rough ruby
discovered at Tan Huong in 1997, sold for
US$290,000 at the Rangoon Gem Emporium
(Myanmar) later that year (Nguyen Xuan An, pers.
comm., 1998). Large star rubies and pink sapphires
are also known. Two pieces (1.96 and 2.58 kg) now
belong to the State Treasurys collection, while DOJI
Gold & Gems Group has preserved an 18.8 kg specimen (figure 5).
For the sake of clarity, we will refer to the original
deposits on the east side of the Chay River as Khoan
ThongAn Phu and to the newer localities on the
west side as Tan HuongTruc Lau (the latter names
are the main mining areas). The older deposits also
have been referred to in the literature as simply Luc
Yen (Kane et al., 1991; Long et al., 2004; Garnier et
al., 2008), while the newer ones have been called Yen
Bai (Long et al., 2004). This terminology is potentially confusing because Khoan Thong, An Phu, and
Truc Lau administratively belong to the Luc Yen
District, while Tan Huong is part of the Yen Binh
District (again, see figure 2). Nevertheless, all of these
184
The Khoan ThongAn Phu and Tan HuongTruc Lau

mining regions lie about 15 km from one another,
but their geologic settings are clearly different. Most
primary and secondary corundum occurrences in the
Tan HuongTruc Lau area are located within the Dy
Ni Con Voi mountain range, which stretches from
Figure 5. The 18.8 kg Great Star Ruby, one of many

large gems mined at Tan HuongTruc Lau, belongs to
DOJI Gold & Gems Group. The stone measures
approximately 32 24 17 cm and has been partly
tumbled and polished to reveal its asterism. Photo by
N. N. Khoi.
GEMS & GEMOLOGY
FALL 2011
KEY
To
QUATERNARY
Sediments
La
Ca
Ch
ay
NEOGENE
Sediments
Khoan Thong
Ri
ve
LO
Lang Chap
PALEOGENE
Tan Huong Complex: biotite granite,
granosyenite, and pegmatite
GA LUC YEN
M
ZO
NE
Truc Lau
TRIASSIC
Nui Chua Complex: pyroxene gabbro,
gabbrodiorite, hornblende diorite
Minh Tien
Phia Bioc Complex: biotite granite,

pegmatite, and aplite
ED
An Phu
NEOPROTEROZOIC-CAMBRIAN
An Phu Formation: graphite-bearing
marble, two-mica schist
IV
ER
SH
EA
Thac Ba Formation: quartz-mica

schist, epidote-biotite-hornblende
schist, marble
Thac Ba
Lake
ZO
N
E
PALEO-MESOPROTEROZOIC
Ngoi Chi Formation: quartz-biotitesillimanite-garnet schist, amphibolite,
marble
Mong Son
Bao Ai
Re
dR
iv
er
Nui Voi Formation: biotite-sillimanitegarnet plagiogneiss, amphibole gneiss,

amphibolites, diopside marble
Kinh La
Figure 6. This simplified

geologic map shows the
locations and rock formations of the corundum
occurrences at Khoan
ThongAn Phu and Tan
HuongTruc Lau.
Modified after Vinh
(2005) and Xuyen (2000).
Smaller deposits are not
shown here.
CORUNDUM DEPOSITS
Tan Huong
To
Khoan ThongAn Phu area (old mines)
Ha
no
Primary
Secondary
Tan HuongTruc Lau area (new mines)
TRAN YEN
R70
0
Primary
Secondary
Fault
Road
10 km
Yen Bai City
Lao Cai Province southeast to Yen Bai Province. The

mountains are bounded by lateral strike-slip faults
(figure 6) forming a major Cenozoic geologic discontinuity in Southeast Asia known as the Ailao
NEED TO KNOW
Northern Vietnams Yen Bai Province has produced ruby and sapphire from adjacent geologically distinct areas referred to as Luc Yen and
Yen Bai.
The latter area pertains to deposits (both primary
and secondary) located on the west side of the
Chay River in the Tan HuongTruc Lau area.
Since the mid-1990s, these deposits have produced mainly cabochon-quality rubies (especially star rubies) and some sapphires.
Although large pieces are known, the corundum
is typically semitransparent to translucent, and
most ranges from pink to purplish or brownish red.
ShanRed River Shear Zone (Trinh et al., 1998, 1999;

Leloup et al., 2001).
Rocks in the Tan HuongTruc Lau area mainly
consist of plagiogneiss and other gneisses intercalat-
ed with lenses of amphibolite and marble; they are

grouped as the Nui Voi Formation (Long et al., 2004;
Nam, 2007; Garnier et al., 2008; again, see figure 6).
These rocks underlie the Ngoi Chi Formation,
which comprises schist, amphibolite, and marble.
Both formations appear to have been intruded by
granite, syenite, and pegmatite of the Tan Huong
magmatic complex, which is 2225 million years old
(Nam and Huyen, 2010).
Primary corundum deposits in the Tan
HuongTruc Lau area can be classified into three
main types:
1. Gray, grayish white to bluish gray, and yellowish gray corundum embedded in gneisses, such
as the Co Man outcrop in Truc Lau valley, and
the Khe Nhan and Kinh La occurrences in the
Tan Huong area (Nam, 2007; Thuyet, 2008).
The corundum usually consists of large (13
cm, with some over 10 cm) well-formed crystals of very low or non-gem quality (Nam, 2007;
Thuyet, 2008; figure 7, left).
2. Dark red to pinkish red rubies of low-to-medium gem quality. These are usually also large
and come from weathered pegmatoid feldspathic rocks (e.g., the occurrences at kilometers 12,
GEMS & GEMOLOGY
FALL 2011
185
Figure 7. The left sample

of corundum-bearing
gneiss, from Co Man, contains mainly feldspar,
biotite, sillimanite, and
sapphire crystals up to 3
cm long. The feldspathic
rock from the Slope 700
outcrop (right) typically
consists of K-feldspar,
biotite, and ruby. Photos
by N. V. Nam.
15, and 23 along National Road 70, and also

Slope 700).
3. Rubies in large marble lenses intercalated within gneiss, mica schist, and amphibolites (e.g.,
the Tan Huong drill core, and DOJIs Truc Lau
mine). This type of ruby appears to have higher
gem quality, but its distribution is limited.
These occurrences, mostly related to gneisses and
schists of metasedimentary origin, are much different from the corundum deposits of Khoan
ThongAn Phu, which are mainly hosted by marble
formations.
The corundum-bearing host rocks in the Tan
HuongTruc Lau area appear to have originated from
the metamorphism of fine-grained sediments of variable composition (Katz, 1972; Simandl and Paradis,
1999). For example, gneisses from the Co Man and
Kinh La outcrops have a wide compositional range,
from 5090% feldspar, up to 40% biotite, and up to
20% sillimanite. In addition, ruby-bearing feldspathic
rocks (e.g., the Slope 700 outcrop) typically consist of
K-feldspar and biotite (or vermiculite; figure 7, right).
The primary host rocks are usually deeply weathered,

forming numerous eluvial deposits.
The secondary (eluvial and alluvial) corundum
deposits usually contain dark red ruby, pink sapphire, and red and brown spinel, as well as some garnet, trapiche-like bluish gray sapphire, sillimanite,
and quartz. Of these mining areas, Truc Lau and Tan
Huong are the most important. Truc Lau occupies a
large valley, about 5 km long, that contains eluvial
and alluvial sediments. The eluvium consists of
three layers: topsoil (averaging 1 m thick); a gembearing layer (0.81 m thick) containing corundum
and spinel that is composed of pebbles, gravel, and
sand; and a deeply weathered gneiss layer (3 m thick)
that typically contains ruby and sapphire. Compared
to the eluvium, the alluvial deposits at Truc Lau are
thicker (~10 m). Ruby, sapphire, and spinel are found
within a gravel paleoplacer (1.25.0 m thick) that
lies on bedrock, and is buried below 0.53.5 m of
Quaternary sediments and 0.51.5 m of topsoil
(figure 8). In 2002, 12 kg per month of pink sapphire
and star ruby were produced from this paleoplacer.
At Tan Huong, the main gem occurrences are
Figure 8. Alluvial layers in the Tan HuongTruc Lau area consist of soil, sandy and pebbly clays,
and gravels containing gem corundum.
Cross-section of alluvial layers
Layer 1
(0.5-1.5 m): Soil
Layer 2
(0.5-3.5 m): Sandy and pebbly clay
with small-sized corundum and spinel
Layer 3
(1.2-5.0 m): Pebbly and sandy gravel
with gem-quality corundum and spinel
Layer 4
Bedrock (gneiss)
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GEMS & GEMOLOGY
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arranged in a northwesterly direction, bounded by

two small lakes. The alluvial deposits consist of a
topsoil layer (~0.5 m thick); a sand horizon with
areas of humus (~0.51 m thick); and a ruby-, sapphire-, and spinel-bearing layer above the bedrock
that contains mixed sand, pebbles, and boulders
(~1.22.5 m thick). All of the alluvial deposits in the
Tan HuongTruc Lau area are quite similar to those
shown in figure 8.
PRODUCTION AND DISTRIBUTION

Current production of gem material from Tan
HuongTruc Lau is about 10 kg per month. This
includes approximately 2030% ruby and some sapphire, and 7080% spinel. Only 1015% of the
stones are of gem quality; the rest are suitable for
carving material or as specimens. Most of the gems
are cut and sold locally. DOJI Gold & Gems Group
is the major exporter of faceted Vietnamese gemstones to the world market, either directly or
through the international gem fairs in Bangkok,
Hong Kong, Tokyo, and Kobe. The main markets for
high-quality corundum are Japan, North America,
and Hong Kong. Large, medium-quality stones are
sold in the Middle East, Taiwan, and Southeast Asia,
while low-quality commercial products go to India
and China.
Heat treatments, including lead-glass filling, have
been applied to these materials, but most appear to
be unsuccessful. After heat treatment, white stripes
often appear along fractures.
MATERIALS AND METHODS

A total of 57 gem samples from Tan HuongTruc
Lau, including 15 rough and 42 cut stones (12
faceted and 30 cabochons), were collected by the
authors over a period of many years, and examined
as summarized in table 1. Among these, 29 cut samples (nine faceted and 20 cabochons) and 10 pieces of
rough were from secondary deposits (e.g., figure 9).
The remaining 13 cut samples (three faceted and 10
cabochons) and five pieces of rough were from primary host rocks (e.g., figure 10) along National Road
70, at kilometers 12, 15, and 23, and at Slope 700.
All of these were gem quality, although those from
primary occurrences typically were of much lower
quality.
We used standard gemological equipment to
record optic character, refractive indices and birefringence, pleochroism, absorption spectra, and UV fluorescence (to long- and short-wave radiation). Specific
gravity was measured by the hydrostatic method

using an electronic balance. Various gemological
microscopes (vertical and horizontal, incorporating
different lighting techniques) were used to observe
internal features.
Raman microspectroscopy was performed on nine
observable mineral inclusions embedded in transparent hosts. The spectra were collected using a Jobin
Yvon LabRam HR 800 spectrometer coupled with an
Olympus BX41 optical microscope and an Si-based
CCD (charge-coupled device) detector at the Institute
of Geosciences, Johannes Gutenberg University
(Mainz, Germany). The samples were excited by a
514 nm Ar-ion laser. The confocal mode was used to
enable analysis at the micron scale (~0.20.5 m).
Absorption spectra of three Tan HuongTruc Lau
rubies were collected using a Shimadzu UV-2450
UV-Vis spectrophotometer at the Center for
Material Sciences, Hanoi University of Science.
Polished thin sections of 23 samples selected
from primary and secondary deposits at Truc Lau
and Tan Huong were prepared for quantitative
chemical analysis by electron microprobe. The analyses were performed using three different instruments, as indicated in table 2. Also analyzed were 29
mineral inclusions exposed on the polished surfaces.
GEMOLOGICAL CHARACTERISTICS
Crystal Morphology. Two main crystal forms characterized the morphology of the corundum from primary deposits:
1. Prismatic crystal habits composed of the hexag
onal prism a {1120} and basal pinacoid c {0001}
2. A modification of this habit, with the addition
of the positive rhombohedron r {1011}

The crystals had short prismatic and sometimes
tabular hexagonal shapes, with a height-to-width
ratio ranging from 1 to 3.
Visual Appearance. In general, rubies and sapphires
from Tan HuongTruc Lau are only of cabochon
quality. Transparent to semitransparent pieces
with more marketable red to pink colors occur in
secondary deposits, while those extracted from primary deposits are usually opaque to translucent
and have dull to dark colors unsuitable for cutting.
Corundum from the primary deposits ranges from
colorless to gray, pale blue, and yellowish to dark
red and violetish pink; only the latter is typically of
gem quality (again, see figure 10). Corundum from
GEMS & GEMOLOGY
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187
TABLE 1. Gemological characteristics of rubies and sapphires from Tan HuongTruc Lau, Vietnam.
Primary deposits
Secondary deposits
Property
No. of samples
Color
13 polished
Pleochroism
13 polished
Diaphaneity
5 rough,
13 polished
Refractive Indices
3 faceted
10 cabochon
Birefringence
Optic character
Specific gravity
UV fluorescencea
3 faceted
3 faceted
5 rough,
13 polished
5 rough,
13 polished
Spectroscope
spectrum
5 rough,
13 polished
Internal features
5 rough,
13 polished
a Abbreviations:
Observations
Colorless, gray to yellowish gray,
bluish or greenish gray
Dark red, red to pink, purplish
pink
Weak to moderate
Dark red to red, pink: Violet to
violetish red, orange to orangy red
Bluish gray: Greenish gray to
bluish gray
Poor to moderate clarity and
opaque to translucent; rarely
semitransparent to transparent
no = 1.7621.763
ne = 1.7701.771
n = 1.761.77 (spot method)
0.0080.009
Uniaxial negative
3.913.99
Gray to white, bluish gray:
Inert to both LW and SW
Red to pink:
LW: Moderate to weak red
SW: Weak red
Red to pink: Chromium spectra
Bluish and greenish gray: 450 nm
(faint line)
Ilmenite, plagioclase, biotite,
muscovite, apatite, zircon, rutile
needles, magnetite, chlorite
Primary and secondary liquid-gas
inclusions
Growth zoning, parting, fractures,
lamellar twinning
No. of samples
Observations
29 polished
Pink, pinkish to purplish and

brownish red, dark red
29 polished
Moderate to strong
Dark red to red, pink: Violet to violetish
red, orange to orangy red
10 rough,
29 polished
Poor to moderate clarity, opaque to

translucent and semitransparent;
some parts may be transparent
no = 1.7621.763
ne = 1.7701.771
n = 1.761.77 (spot method)
9 faceted
20 cabochon
9 faceted
9 faceted
10 rough,
29 polished
10 rough,
29 polished
0.0080.009
Uniaxial negative
3.924.07
10 rough,
29 polished
Red to pink: Chromium spectra
10 rough,
29 polished
Rutile (needles, silk, clouds, and

stringer formations), ilmenite, zircon, apatite, spinel, diaspore, plagioclase, biotite, muscovite, chlorite, allanite(?), magnetite
Primary and secondary liquid-gas
inclusions
Growth zoning, parting, fractures,
lamellar twinning
Red to pink:
LW: Moderate to strong red
SW: Weak to moderate red
LW = long-wave, SW = short-wave.
Figure 9. These rough and cut rubies are from secondary deposits at Truc Lau. The cabochons on the right
range from 8.24 to 19.53 ct. Note the asterism in the stone on the lower right. Photos by N. N. Khoi.
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GEMS & GEMOLOGY
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Figure 10. This ruby crystal (2.45 g) formed in feldspathic host rock (see figure 7, right). Photo by N. V. Nam.
the secondary deposits, however, has more desirable colors that commonly range from dark red,
brownish red, and violetish to pinkish red (figures 1
and 11). The secondary deposits also yield sapphires
that are usually colorless, yellowish gray, bluish
gray, or multicolored. Blue, green, and yellow hues
are very rare. Diaphaneity ranges from opaque to
nearly transparent.
The corundums dimensions vary considerably,

from several millimeters to several centimeters. The
most significant visual features are growth zoning
(straight and angular) and asterism (figure 12); about
30% of the gem-quality stones show a star phenomenon, according to the miners. Color irregularities such as spots, streaks, and patches are uncommon in these rubies and sapphires.
Another distinct characteristic of corundum
(especially ruby) from both primary and secondary
deposits in Tan HuongTruc Lau is an overgrowth
of iron-stained spinel. These coated stones have an
unsightly yellowish gray appearance until the
spinel crust is cut away to reveal a red core of ruby
(figure 13). Local gem dealers call the spinelencrusted material hng m bt (gamble merchandise), indicating the uncertainty of dealing with
these goods.
Optical Characteristics and Specific Gravity. The
refractive indices, birefringence, and specific gravity
values of ruby and sapphire from Tan HuongTruc
Lau fell within typical values for corundum, and
there was little difference in these properties
TABLE 2. Summary of electron microprobe analyses of corundum from Tan HuongTruc Lau, Vietnam.a
Primary corundum
Oxide
(wt.%)
Al2O3
SiO2
TiO2
Cr2O3
FeO
MnO
MgO
NiO
CaO
Na2O
K2O
V2O5
ZnO
Ga2O3
Total
Secondary corundum
Bluish gray to pale

blue, from Truc Laub
(10)
Pale pink,
from Truc Lauc
(3)
Pink to red,
from Truc Lauc
(4)
Dark red,
from Tan Huongd
(1)
Violetish red to violetish

pink, from Tan Huongd
(5)
97.1298.95
nd0.10
nd0.05
nd0.04
0.941.38
nd0.02
nd0.02
nd0.04
nd0.04
nd0.02
nd0.03
nd0.23
99.0099.30
nd0.10
nd0.22
0.110.44
0.150.48
98.9099.30
nd0.05
0.070.69
0.030.37
99.76
0.18
98.9099.98
0.0140.11
0.690.27
0.0050.15
nd0.12
nd0.04
99.51
99.84
99.67
99.94
100.16
Number of samples shown in parentheses; average of 45 analyses per sample. Total iron is reported as FeO. Abbreviation: nd = not detected.
b
Analyzed at Vietnam Institute of Geosciences and Mineral Resources, using a JEOL JXA 8800R/8900 microprobe with an accelerating voltage of 15
kV, a beam current of 1.2 nA, and a collection time of 20 seconds (major elements) or 15 kV, 50 nA, and 80 seconds (trace elements).
c
Analyzed at the Institute of Geology, Russian Academy of Science, using a Camebax-Kevex microprobe with an accelerating voltage of 15 kV, beam
current of 20 nA, and collection time of 20 seconds.
d
Analyzed at the Earth Sciences Institute, Academia Sinica, Taiwan, using a JEOL JXA 8900-R microprobe with an accelerating voltage of 15 kV, a
beam current of 20 nA, and a collection time of 20 seconds.
GEMS & GEMOLOGY
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189
Figure 11. These red to pinkish red rubies (4.2614.58

ct) are from alluvial deposits in the Tan HuongTruc
Lau area. Note the asterism in some of the stones.
Photo by N. N. Khoi.
between primary and secondary corundum (table 1).

Although high-SG mineral inclusions were common
in corundum from the primary deposits, some samples from the secondary deposits actually had higher
SG values (up to 4.07, versus 3.99). This may be
caused by a higher content of heavy inclusions such
as ilmenite.
Figure 12. Growth zoning and asterism are often

observed in corundum from secondary deposits in
the Tan HuongTruc Lau area. These samples range
from 13.77 to 24.54 ct. Photo by N. N. Khoi.
Internal Features. The majority of the gem-quality

samples were from secondary deposits, which we
aimed to separate from the Khoan ThongAn Phu
gem materials. Nevertheless, some samples from the
primary deposits were investigated for comparison.
These contained various mineral inclusions, such as
ilmenite, plagioclase, biotite, muscovite, apatite, zircon, rutile, magnetite, and chlorite. Among these,
ilmenite, biotite, and magnetite were the most common. Primary and secondary gas-liquid inclusions
were also encountered frequently.
The most common mineral inclusions in samples from secondary deposits were rutile, ilmenite,
zircon, apatite, spinel, and diaspore; some plagioclase and mica (biotite and muscovite) were also
observed. The rutile usually occurred as short needles, but also seen were tiny rutile inclusions with a
silk-like appearance that formed antenna-like patterns (figure 14).
In general, the range of mineral inclusions was
similar between the primary and secondary samples.
Ilmenite was typical, and easily recognized by its
stubby crystal shape, black color (figure 15, left), and
submetallic luster when exposed to the surface.
Apatite (figure 15, right) and zircon were also frequently encountered in our samples, forming nearcolorless euhedral crystals. In addition, we observed a
wide range of fluid inclusions that often showed various stages of healing, forming negative crystals (figure
16), fingerprints, feathers, folded patterns, and irregular fluid droplets. Iron stains were also apparent.
Figure 13. Rubies from secondary deposits at Tan

HuongTruc Lau are often coated by an iron-stained
spinel aggregate. Here the spinel overgrowth has partially broken away from a ruby crystal (~2 cm across) after
the specimen was sawn open. Photo by N. V. Nam.
190
GEMS & GEMOLOGY
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Figure 14. Rutile inclusions,

usually as short needles oriented in three directions
(left), may contribute to the
asterism in some of the
corundum. Rutile inclusions
may also show a silky
appearance (left) or antennalike patterns (right). Photomicrographs by N. N. Khoi;
magnified 45.
Optical phenomena such as asterism, chatoyancy,

and sheen were caused by oriented micro-inclusions,
rutile needles in particular. The star effect in many of
the rubies was quite sharp and attractive. Straight
and angular growth zones, typically sharp and well
defined, were conspicuous in most stones. Asterism
and growth structures were observed together in
some instances (figure 17, left). Three systems of
polysynthetic lamellar twinning parallel to the posi
tive rhombohedron r {1011} were quite common (figure 17, right). Fracturing along these twin planes
yielded parallelogram-shaped rough material.
Absorption Spectra. Preliminary observation of the
ruby samples with the desk-model spectroscope
showed essentially the same features as the diagnostic absorption spectra described by Liddicoat (1993)
for natural and synthetic rubies and purple sapphire.
The strong lines at 692 and 694 nm often appeared
as a single bright emission line at 693 nm. UV-Vis
absorption spectroscopy (figure 18) showed peaks at
~378, 389, and 456 nm related to iron (Fe3+ and Fe2+).
A broad band centered around 570 nm, related to

Fe 2+/Ti 4+, also appeared in these spectra. Cr 3+ features were evidently superimposed by the iron
absorptions.
Chemical Analysis. Microprobe analyses of sapphires from primary deposits (table 2) showed relatively high contents of iron, especially in bluish gray
stones (0.151.38 wt.% FeO). Chromium contents
ranged from low (<0.04 wt.% Cr2O3) in bluish gray
sapphires to moderate (0.110.44% Cr2O3) in the
pink sapphires. Titanium contents ranged up to 0.22
wt.% TiO2. In addition, some samples showed very
small amounts of Si, Ca, K, Na, Ni, and Zn, probably
due to tiny mineral inclusions.
The trace-element compositions of stones from
placer deposits were similar to those from primary
deposits. Their varying proportions clearly corresponded to differences in color. Greater contents of
Cr were recorded for pink sapphires and rubies. In
general, both rubies and sapphires from Tan
HuongTruc Lau had high Fe contents.
Figure 15. Ilmenite is a

typical inclusion in ruby
and sapphire from Tan
HuongTruc Lau, and usually shows a stubby shape
and black color (left).
Apatite typically occurs as
colorless to light-colored
euhedral crystals, as
shown on the right.
Photomicrographs by
N. N. Khoi; magnified 45.
GEMS & GEMOLOGY
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191
logical properties (Khoi, 2004; Khoi et al., 2010a,b),

as discussed below.
Figure 16. Negative crystals are quite common in

ruby and sapphire from Tan HuongTruc Lau, usually distributed along fractures and fissure planes. Two
phases (gas and liquid) were occasionally observed in
these inclusions. Photomicrograph by N. N. Khoi;
magnified 45.
DISCUSSION
Although gem corundum from Tan HuongTruc
Lau, especially star ruby, has been sold in the world
market for more than 10 years, these Vietnamese
deposits remain largely unknown. Many in the trade
assume the stones are from Luc Yen (i.e., Khoan
ThongAn Phu), but those belong to different geologic settings and consequently have distinctive gemo-
Morphology and Appearance. In contrast to the short

prismatic and sometimes tabular morphologies of
corundum from Tan HuongTruc Lau, crystals from
Khoan ThongAn Phu typically have a barrel or
spindle shape with n, z, and hexagonal dipyramids,
r rhombohedra, and c pinacoidal faces with lengthto-width ratios from 5 to 6 (Long, 2003; Nam, 2007;
Thuyet, 2008). The most distinctive feature of the
Tan HuongTruc Lau corundum is its coating of
granular spinel (Hger et al., 2010; Hauzenberger et
al., 2010). Also, pieces of rough from Tan
HuongTruc Lau are generally much larger than
those from Khoan ThongAn Phu.
The majority of cut stones from Khoan
ThongAn Phu range from pure red or pink to purplish red or pink; other hues such as blue, orangy
red, violet, or multicolored are also found with varying tones and saturations. Both rough and polished
stones commonly have strong color zoning visible to
the unaided eye. Diaphaneity usually ranges from
transparent to translucent (Kane et al., 1991; Long,
2003; Khoi et al., 2010a). In contrast, corundum from
Tan HuongTruc Lau shows less color variation,
mostly consisting of pink to purplish or brownish
red hues. Color zoning is uncommon. Diaphaneity is
commonly semitransparent to translucent or opaque
because of fracturing and the abundance of inclusions. Interestingly, some features typical of this
Figure 17. Asterism and growth structures are seen in this 14.45 ct pink sapphire from Truc Lau (left).
Polysynthetic twinning, parallel to the positive rhombohedron r {1011}, is a common feature of ruby
and sapphire from Tan HuongTruc Lau (right). Photomicrographs by N. N. Khoi; magnified 12.
192
GEMS & GEMOLOGY
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TABLE 3. Comparison of internal features in corundum

from Tan HuongTruc Lau and Khoan ThongAn Phu,
Vietnam.a
UV-VIS-NIR ABSORPTION SPECTRUM

3.2
ABSORBANCE
378
2.8
Internal feature
389
456
2.4
570
2.0
400
500
600
700
800
WAVELENGTH (nm)
Figure 18. This UV-Vis-NIR spectrum of a ruby from a

primary deposit at Truc Lau is dominated by Fe-related
absorptions.
corundum (large size, asterism, and angular growth

structures) are also seen in ruby crystals from
Karnataka, India (Panjikar et al., 2009).
Internal Features. A summary of mineral inclusions
in corundum reported from both mining areas is presented in table 3. The most common mineral inclusions in Khoan ThongAn Phu corundum are calcite,
rutile, apatite, spinel, zircon, corundum, pyrrhotite,
graphite, boehmite, hematite, phlogopite, muscovite,
hercynite, tourmaline, and iron oxide or hydroxide
(Kane et al., 1991; Long, 1999; Long et al., 2004; Khoi
et al., 2010a,b). Straight, angular color zones and colored patches and spots are usually seen in the blue
sapphires, and swirl growth marks are observed occasionally (see Kane et al., 1991; Long et al., 2004).
Gem corundum from Tan HuongTruc Lau contains a diversity of mineral inclusions, most commonly ilmenite, rutile, apatite, zircon, diaspore,
boehmite, magnetite, plagioclase, biotite, muscovite, and chlorite. Although straight and angular
growth structures are quite common, color irregularities are rare. Trapiche rubies and pink sapphires
are also known from this region (Schmetzer et al.,
1996), but were not examined for this report.
The common polysynthetic twinning in corundum from the Tan HuongTruc Lau area may be
related to deformation from the Red River Shear
Zone (Khoi et al., 2010b).
CONCLUSIONS
For more than two decades, Vietnam has been an
important source of gem ruby and sapphire. Most of
Tan HuongTruc Laub
Solid Inclusions
Anatase
Anhydrite
Apatite
Biotite
Boehmite
Calcite
Chlorite
Corundum
Diaspore
Dolomite
Graphite
Halite
Hematite
Hercynite
Ilmenite
Iron oxide or
hydroxide
Magnetite
Margarite
Monazite
Muscovite
Nepheline
Nordstrandite
Phlogopite
Plagioclase
Pyrite
Pyrrhotite
Rutile (primary)
Rutile needles
(silk, cloud)
Sphene
Spinel
Tourmaline
Zircon
Liquid Inclusions
Fingerprints
Negative crystals
Salts (Na, Ca,
K chlorides)
Other Features
Color zoning
Growth structures
Twinning
Swirl growth marks
Wedge-shaped
growth features
++
+
+
Khoan ThongAn Phuc

+
+
++
+
+++
+
+
+
+
+
+
+
+
+
++
+++
+++
++
+
+
+
+
+
+
+
+
+
++
+
+
+
++
+
+
+
+
+
++
++
+
++
+
+
+
++
+
++
++
+
+
+
Symbols: +++ = common, ++ = frequently encountered, + =

encountered.
From this study.
c References: Kane et al. (1991), Long (1999), Vinh et al. (1999), Dao
and Delaigue (2001), Giuliani et al. (2003), and Long (2003).
b
the production has come from Yen Bai Province; the

original deposits in the Khoan ThongAn Phu area
and the newer ones in Tan HuongTruc Lau are con-
GEMS & GEMOLOGY
FALL 2011
193
sidered to have the most potential (see figure 19).

Despite their proximity, the two areas belong to different geologic settings (marble- and gneiss-hosted,
respectively). The Tan HuongTruc Lau deposits are
mostly restricted to the Dy Ni Con Voi mountain
range, which is associated with the Red River Shear
Zone. Recent mining activities mostly consist of
sporadic diggings by local people, though a few
mechanized pits are active.
Gem corundum from Tan HuongTruc Lau usually shows a tabular crystal form with deformed
polysynthetic twinning along rhombohedral faces
and sharp growth zones. Their typical colors range
from pink to pinkish red. Color irregularities such as
zoning and spots or patches are rare. Many stones,
particularly the sapphires, have low transparency due
to abundant fracturing and inclusions. The density of
mineral inclusions appears crucial to differentiating
these stones from those from the Khoan ThongAn
Phu deposits. The most common mineral inclusions
in the Tan HuongTruc Lau stones are clusters of
tiny short rutile needles, black stubby ilmenite, euhedral apatite, and assemblages of various minerals (e.g.,
ilmenite, rutile, and zircon), often in the same stone.
Although the vast majority of gem corundum
from Tan HuongTruc Lau is suitable for cutting
cabochons (including star rubies) rather than faceted
stones, some exceptionally large pieces of rough containing gem-quality areas are known. The deposits
Figure 19. This ring is set with a 17.50 ct star ruby from
Truc Lau. The star is sharp and complete throughout the
stone. Jewelry courtesy of DOJI Gold & Gems Group;
photo DOJI Gold & Gems Group and N. N. Binh.
show strong potential for producing commercial

quantities of gem corundum for many years. The
main markets for gem material from the Tan
HuongTruc Lau area are Japan, the Middle East, and
India.
ABOUT THE AUTHORS

Dr. Khoi is a gemologist and associate professor of geology,
Dr. Thuyet is a geologist, and Dr. Nhung is a retired associate professor, at the Hanoi University of Science, Vietnam National
University. Dr. Khoi is also the director of the DOJI Laboratory for
Gemology and Jewelry (DOJI Gold & Gems Group, Hanoi). Dr.
Sutthirat (c.sutthirat@gmail.com) is an assistant professor of geology in the Faculty of Science, Chulalongkorn University, Bangkok,
and an academic advisor for the Gem and Jewelry Institute of
Thailand in Bangkok. Mr. Tuan is vice general director of DOJI Gold
& Gems Group. Mr. Nam holds a masters degree in geology from
the Vietnam Institute of Geosciences and Mineral Resources, Hanoi.
194
ACKNOWLEDGMENTS
This work has been supported over a number of
years by Vietnam National University, Hanoi
(Projects QG-08-13 and SXT10.01), the Gem
and Jewelry Institute of Thailand, and the
Geology Department of Chulalongkorn
University. We thank DOJI Gold & Gems Group
and its technical staff for their assistance with
this work. We are also grateful to Teaching and
Research Improvement Grants from the Hanoi
University of Science at Vietnam National
University for financial support.
GEMS & GEMOLOGY
FALL 2011
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Hanoi, April 410, pp. 4078.
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GEMS & GEMOLOGY
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195
INFRARED SPECTROSCOPY OF NATURAL VS.

SYNTHETIC AMETHYST: AN UPDATE
Stefanos Karampelas, Emmanuel Fritsch, Triantafillia Zorba, and Konstantinos M. Paraskevopoulos
When microscopic identification is not feasible,

FTIR spectra at high resolution (0.5 cm1) can distinguish natural and synthetic amethyst. The 3595
cm1 band is characteristic of natural amethyst and
has a full width at half maximum (FWHM) of 3.3
0.6 cm1. In synthetic amethyst, this band is either
absent or (very rarely) about twice as broad.
Exceptions to this criterion include natural amethyst
with pronounced near-colorless zones, which do
not always display this band, and natural specimens
that either have an intense, unusually broad 3595
cm1 band or show total absorption in the X-OH
region (38003000 cm1) of the spectrum.
em-quality amethyst is found on all continents and in various geologic environments

(figure 1). Some contemporary sources are
Brazil, Uruguay, Zambia, Namibia, Mexico, Russia,
Arizona, Canada, Bolivia, and Sri Lanka (Shigley et
al., 2010). Synthetic amethyst crystals are grown in
either a near-neutral NH4F solution (see figure DD-1
in the G&G Data Depository at gia.edu/gandg) or an
alkaline K2CO3 solution (figure 2). The identification
of NH4F-grown synthetic amethyst is straightforward with standard microscopy (observation of color
zoning; figure DD-2) or infrared spectroscopy
(Balitsky et al., 2004b; figure DD-3). However, most

196
NOTES AND NEW TECHNIQUES
synthetics in the market today are grown in K2CO3

solution (cited below simply as synthetic
amethyst). Classical gemological techniques (observation of twinning, color zoning, and inclusions) can
distinguish only some of these synthetics
(Crowningshield et al., 1986; Notari et al., 2001, and
references therein). The highest-quality products are
free of inclusions, distinct color zoning, and in many
cases twinning, which makes their identification
more challenging.
Recent investigations have demonstrated the effectiveness of laser ablationinductively coupled plasmamass spectrometry (LA-ICP-MS) in separating
natural and synthetic quartz. Plots of Ti+Cr vs. Ga are
reportedly the most useful (Breeding and Shen, 2010).
Unfortunately, this technique is not widely available
and is too expensive to use for the identification of a
common gem such as amethyst. Furthermore, overheating from the ablation laser may cause cracks in
the samples (L. Klemm, pers. comm., 2011).
Infrared absorption spectroscopy in the region of
X-OH stretching vibrations (i.e., 38003000 cm1)
has long been considered useful for distinguishing
natural and synthetic amethyst (Smaali, 1998;
Zecchini and Smaali, 1999; Notari et al., 2001;
Balitsky et al., 2004a,b; Karampelas et al., 2006, and
references therein). In this region, the infrared spectra of natural and synthetic amethyst are largely
similar, though they have some important differences. The specific range of interest is from 3640 to
3500 cm1, where both show absorptions at approximately 3612 and 3585 cm1. These two absorptions
are probably due to vibrations caused by Al substitutions (Kats, 1962).
Earlier studies used bands at 3595 and 3543 cm1
GEMS & GEMOLOGY
FALL 2011
Figure 1. Determining
the natural or synthetic
origin of some amethyst
remains a challenge for
gemologists. Shown here
are three natural samples weighing 22.0043.79 ct (at left; GIA
Collection nos. 13143,
37216, and 31971) and a
4.89 ct synthetic (the
emerald cut at lower
right, GIA Collection
no. 17239) in front of
various samples of undetermined origin. Photo
by Robert Weldon.
to separate natural and synthetic amethyst. The

band at 3543 cm1, observed in the vast majority of
lab-grown amethyst, was considered indicative of
synthesis (Fritsch and Koivula, 1988). However,
stones from a number of natural deposits can also
show this absorption (Kitawaki, 2002), which is
related to the negative rhombohedron growth sector
rather than synthesis (Balitsky et al., 2004a,b).
Likewise, the 3595 cm1 band observed in most natural amethyst was once considered indicative of nat-
ural origin (Zecchini and Smaali, 1999, and references therein), but this band was subsequently noted
in the spectra of some synthetic amethyst (Notari et
al., 2001; Karampelas et al., 2005, 2006), and was
reported to be absent from some natural samples
(Balitsky et al., 2004a,b). FTIR measurements at high
resolution (0.5 cm1) found that this band is present
in all natural amethyst, but can be missed with standard 4 cm1 resolution. In synthetic amethyst, this
band is either absent or (rarely) when present has a
Figure 2. These
K2CO3-grown synthetic
amethysts include an
unusual Russian prismatic cluster (left; 10
cm tall) and a crystal
weighing more than 1
kg (right; 15 cm tall).
The vast majority of
synthetic amethyst in
the gem market is
K2CO3 grown. Photos
by Franck Notari.
GEMS & GEMOLOGY
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197
TABLE 1. Comparison of the 3595 cm1 band in natural and

synthetic (K2CO3 grown) amethyst.
Sample
no.
Am008
Am082
Am106
Am016
Am448
Q022
Am060
Ru007
Uru007
Am068
Am075
Am080
Am023
Am057
Q198
Am169
Am004
Am585
Am4
Am1612
Am177
a
Origin
Bolivia (Anah)
Bolivia (Anah)
Brazil (Marab)
Brazil (Pau dArco)
France (St. Raphael)
Japan (Ishikawa)
Mexico (Veracruz)
Russia (Urals)
Uruguay (Artigas)
USA (Four Peaks,
Arizona)
Zambia (Solwezi)
Zambia (Solwezi)
Unknown
Unknown
Japan
Russia
Russia (prismatic)
Russia
Russia
Russia
Russia
Type
Weight
(ct)
No.
scansa
FWHM
(cm 1)
Natural
Rough
Rough
Rough
Rough
Rough
Faceted
Faceted
Rough
Rough
Rough
0.4
4.1
5.3
0.8
1.0
2.3
3.0
1.0
0.4
3.4
128 or 512
128 or 1024
128 or 1024
200 or 300
128 or 512
512 or 512
128 or 1024
128 or 512
128 or 512
128 or 1024
2.7
3.2
3.3
3.5
3.0
3.0
3.3
3.0
3.9
3.0
Rough
Faceted
Faceted
Faceted
3.8
4.0
1.2
2.9
150 or 300
128 or 512
200 or 700
200 or 700
3.5
3.5
5.0
5.0
Synthetic
Faceted
3.1
Faceted
8.5
Rough
0.2
Faceted
29.3
Faceted
16.0
Faceted 8060.0
Faceted
8.9
300 or 900
128 or 1024
256 or 1024
128 or 1024
128 or 1024
128 or 1024
128 or 1024
At 4 or 0.5 cm 1 resolution, respectively.
FWHM value approximately two times larger than

that of natural specimens (Karampelas et al., 2005,
2006).

This study was carried out on 21 samples, 14 natural
and seven synthetic. Several geographic localities
were represented, including some that did not satisfy
the proposed IR separation criteria given in previous
studies. The natural identity of two samples of
unknown origin was confirmed microscopically. All
the synthetic amethyst samples in this study were
grown in alkaline K2CO3 solutions, including rare
and unusual prismatic material (figure 2, left). Nine
samples were faceted and 12 were rough (for details
on their size and origin, see table 1). All were
obtained from reputable sources (see Acknowledgments), and none contained near-colorless zones.
Infrared absorption spectra of the faceted and
some of the rough samples were acquired with a
Bruker Vertex 70 FTIR spectrometer (under vacuum)
at the University of Nantes, and a Varian 640 FTIR
spectrometer at the Gbelin Gem Lab, both using a
diffuse reflectance accessory as a beam condenser.
198
A Bruker 113v FTIR spectrometer (under vacuum) in

the Physics Department of Aristotle University was
used for measurements on some of the rough samples. The spectra were taken in random crystallographic orientation, as the bands of interest are littleaffected by direction (see Karampelas et al., 2005).
Previous studies found that the true shape of the
3595 cm1 band is obtained at a resolution of 0.5
cm1 (Karampelas et al., 2005; figure DD-4). Thus,
we measured the samples at 0.5 cm1, as well as at
the standard 4 cm1 resolution. To obtain a high signal-to-noise ratio, multiple scans were collected
(again, see table 1). When the 3595 cm1 band was
present, we measured its FWHM (see figure DD-5 for
more information on this process).
RESULTS AND DISCUSSION

IR absorption spectra in the 36403500 cm1 range
are presented in figures 35 (and DD-6 through DD-
NEED TO KNOW
Standard gemological testing is not always sufficient to identify synthetic amethyst.
High-resolution (0.5 cm-1) FTIR analysis has
shown that the band at 3595 cm-1 is present in
the vast majority of natural amethyst.
While the 3595 cm-1 band can occur in synthetic
amethyst, it has a much larger FWHM value than
in natural specimens.
10). The spectra corresponding to the two different

resolutions are stacked and offset in absorbance for
clarity. In these figures, the upper spectra are taken
at a resolution of 0.5 cm1, and the lower ones with a
4 cm1 resolution. The expected absorption bands at
3614 and 3585 cm1 were observed in all samples,
natural and synthetic. The 3543 cm1 band was
observed in five of the natural and all of the synthetic amethyst (see figure 3 and also figures DD-6 and
DD-7).
The 3595 cm1 band was visible in some natural
amethyst at 4 cm1 resolution and in all of them at
0.5 cm1 resolution (see figure 4 and also figures DD8 and DD-9). In some samples, this band was very
intense (figures 5 and DD-10). The band did not
appear in the spectra of any of the synthetic
GEMS & GEMOLOGY
FALL 2011
IR ABSORPTION SPECTRA
3.2
3585
3595
3585
0.65
ABSORBANCE
ABSORBANCE
2.8
0.55
3543
0.45
3614
2.4
2.0
3562
3614
1.6
0.35
1.2
0.25
3640
3620
3600
3580
3560
3540
3520
3500
0.8
3640
3620
3600
WAVENUMBER (cm )
Figure 3. The infrared absorption spectra of a rare 0.2 ct

rough prismatic synthetic amethyst from Russia
(Am004; see figure 2, left) are shown at resolutions of 4
cm 1 (red) and 0.5 cm 1 (black). The 3595 cm 1 band is
not observed, but a shoulder is present at 3543 cm 1.
amethyst studied here, though it did in a sample

from a previous study (Karampelas et al., 2005).
Some natural material from (Marab) Brazil shows
total absorption in the ~3600 to 3000 cm1 region,
but this has been documented as being characteristic
of natural amethyst (Smaali, 1998). In a previous
Figure 4. The infrared absorption spectra of a 3.8 ct
rough amethyst from Zambia (Am075) are shown at
resolutions of 4 cm 1 (red) and 0.5 cm 1 (black). The
3595 cm 1 band is barely visible at 4 cm 1 but well
resolved at 0.5 cm 1 (FWHM of 3.5 cm 1).
3.2
3585
ABSORBANCE
2.8
2.4
3595
2.0
3614
1.6
1.2
0.8
0.4
3640
3620
3600
3580
3560
3540
-1
WAVENUMBER (cm )
3580
3560
3540
3520
3500
WAVENUMBER (cm-1)
-1
3520
3500
Figure 5. The infrared absorption spectra of a 2.9 ct

rough amethyst of unknown origin with natural inclusions (Am057) are shown at resolutions of 4 cm 1 (red)
and 0.5 cm 1 (black). The 3595 cm 1 band is more
intense than the one at 3585 cm 1 in both spectra, with
an FWHM of 5 cm 1 at 0.5 cm 1 resolution. A shoulder
at about 3562 cm 1 is observed at both resolutions.
study, a sample that presented total absorption in

this region was cut into two halves, which both displayed the 3595 cm1 band (as well as those at 3585
and 3614 cm1; Karampelas, 2002). Some natural
amethyst from other localities (e.g., Solwezi,
Zambia) also shows strong absorption (i.e., a high
absorption coefficient) in this region. Relatively
small pieces (<10 ct) of natural amethyst with a high
absorption coefficient can show total absorption in
the ~3600 to 3000 cm1 region. To date, no known
synthetic amethyst (even large samples; figure DD-7)
presents total absorption in this region. However,
more samples of synthetic amethyst need to be studied to strengthen these findings.
The natural amethyst FWHM values of the 3595
cm1 band at 0.5 cm1 resolution are similar to those
previously published (3.3 0.6 cm1; Karampelas et
al., 2006). Some larger 3595 cm1 bands recorded in
this study (FWHM: 5.0 cm1) were obtained from samples in which the 3595 cm1 band was more intense
than the 3585 cm1 band (again, see figures 5 and DD10). Very intense bands at 3595 cm1 have also been
measured in rock crystal quartzes from Norway and
Japan (Nimi et al., 1999; Mller and Koch-Mller,
2009). Although some natural samples with colorless
bands do not show absorption at 3595 cm1, most of
those can be identified with classical gemology (e.g.,
GEMS & GEMOLOGY
FALL 2011
199
CONCLUSION
When classical gemological techniques are inconclusive, FTIR spectroscopy at high resolution (0.5 cm1)
can provide a criterion of demonstrated validity in
separating the material currently on the market (figure 6), including some rare and unusual synthetics. If
there is no 3595 cm1 absorption, or if it has an
FWHM of 7 cm1 or more, the sample is synthetic. If
the 3595 cm1 band has a width of 3.3 0.6 cm1, the
sample is natural. If the 3595 cm1 band is more
prominent than the 3585 cm1 band, its FWHM can
be larger. Total absorption in the X-OH region
(38003000 cm1) occurs only in natural amethyst
and has not been observed to date in synthetic mate-
ABOUT THE AUTHORS

Dr. Karampelas (s.karampelas@gubelingemlab.ch) is a
research scientist at the Gbelin Gem Lab, Lucerne,
Switzerland. Dr. Fritsch is professor of physics at the
Institut des Matriaux Jean Rouxel (IMN)-CNRS, Team
6205, University of Nantes, France. Mrs. Zorba is a
research analyst, and Dr. Paraskevopoulos is professor
of physics, at the Aristotle University of Thessaloniki,
Greece.
3595
1.6
3585
Natural
ABSORBANCE
observations of twinning and color zoning).

The exact cause of the 3595 cm1 band in amethyst is unknown (Staats and Kopp, 1974; Nimi et
al., 1999; Miyoshi et al., 2005; Lameiras et al., 2009;
Thomas et al., 2009; Mller and Koch-Mller, 2009).
This OH band has been linked to the presence of
boron in synthetic quartz (Staats and Kopp, 1974),
and more recently it was observed in the spectra of
B-doped synthetic quartz with an FWHM of about 7
cm1 (at 2 cm1 resolution; Thomas et al., 2009). The
same OH band was attributed to structural B-related defects in the lattice of natural quartz (Mller and
Koch-Mller, 2009). To the best of our knowledge,
however, B-doped synthetic amethyst is not present
in the gem market. Additional research is needed to
find the exact cause of the slight differences in the
FWHM of the 3595 cm1 band in natural and synthetic amethyst.
1.2
3614
Natural
0.8
Synthetic
Synthetic
0.4
0
3640
3620
3600
3580
3560
3540
3520
3500
-1
WAVENUMBER (cm )
Figure 6. Shown here are infrared absorption spectra at

0.5 cm 1 resolution of two synthetic amethysts (green:
Am006, and red: K2CO3-grown from Russia, not presented in table 1 but published in Karampelas et al., 2005)
and two natural specimens (black: Am060, and blue:
Am023). In the synthetics, the 3595 cm 1 band is either
absent (green) or has an FWHM of 7 cm 1 (red). Natural
amethyst typically has the 3595 cm 1 band with an
FWHM of 3.3 0.6 cm 1 (black). However, some natural
samples have a 3595 cm 1 band that is more intense
than the one at 3585 cm 1, with an FWHM of 5 cm 1 at
0.5 cm 1 resolution (blue).
rial. The IR criteria cited above are only valid for

amethyst that does not have large near-colorless
zones. The 3595 cm1 band may be due to a boronrelated defect in the amethyst lattice.
ACKNOWLEDGMENTS
The authors thank E. Petsch (Idar-Oberstein, Germany), the
Laboratoire Franais de Gemmologie (Paris, France), the former Gemmological Association of All Japan (GAAJ)-Zenhokyo
Laboratory (Tokyo, Japan), Frank Notari (Gemlab-Gemtechlab
Laboratories, Geneva, Switzerland), and the Centre de
Recherches Gemmologiques (Nantes, France) for providing
samples for this study. Dr. Leo Klemm (Gbelin Gem Lab)
provided technical information regarding LA-ICP-MS analysis.
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GEMS & GEMOLOGY
FALL 2011
201
EXPLORING THE ORIGIN AND NATURE

OF LUMINESCENT REGIONS
IN CVD SYNTHETIC DIAMOND
Bert Willems, Alexandre Tallaire, and Julien Barjon
In the DiamondView instrument, blue to bluegreen luminescent zones may be seen in CVD
synthetic diamond when the growth run has
been interrupted and resumed, a well-known
practice in the production of gem-quality CVD
synthetics. DiamondView, photoluminescence
(PL), and cathodoluminescence (CL) imaging
were applied to study the origin and nature of
these luminescent regions in two samples of
high-purity single-crystal CVD synthetic diamond. DiamondView and PL measurements
showed a correlation with silicon-related centers.
In addition, CL analysis confirmed the presence
of boron. Both silicon and boron showed preferential incorporation at the interface between
CVD layers, where a higher uptake of impurities
lead to the observed luminescence. Although the
growth interruptions cannot be detected with the
naked eye, the growth history can be determined
accurately using luminescence imaging and
spectroscopy techniques.
uminescence spectroscopy and imaging are

important techniques for characterizing optical
defects in diamond. The luminescence characteristics of diamond have been studied extensively
and have provided insight into associated optical
See end of article for About the Authors.

202
defect centers (see, e.g., Walker, 1979; Collins, 1992).

The Laboratoire des Sciences des Procds et des
Matriaux (LSPM; formerly known as Laboratoire
dIngnierie des Matriaux et des Hautes Pressions,
LIMHP) near Paris grows high-purity, unintentionally doped single-crystal chemical vapor deposition
(CVD) synthetic diamond for high-power electronic
devices (Kone et al., 2010). As part of the fabrication
process for such applications, several active layers
may be grown in different CVD reactors (Denisenko
and Kohn, 2005), which requires that the growth run
be interrupted and resumed in cycles. Although the
CVD synthetic diamond samples studied here were
thin plates rather than faceted gems, the same
approach is applicable to the production of gemquality CVD synthetic diamonds (figure 1), as it
enables the growth of thick single crystals in three
dimensions (Ho et al., 2006) and offers a method to
control the bulk crystalline quality (Friel et al.,
2009). The present study focuses on the luminescence generated by optical defect centers occurring
in the process of these growth interruptions and
resumptions (with pre- or intermediate etching
steps). As such, gemologists can acquire in-depth
information about the origin and growth history of
these synthetic diamonds, which is crucial in differentiating them from natural material.

The two synthetic diamond samples investigated
here were grown at LSPM-CNRS using the plasmaassisted CVD method (Achard et al., 2005). Sample
A was synthesized in a microwave plasma reactor
operating at 2.45 GHz. A previously etched HPHTgrown type Ib (100)-oriented synthetic diamond was
GEMS & GEMOLOGY
FALL 2011
used as the substrate. The growth was performed in

two runs under high-power conditions (3 kW, 200
millibars, 850C, 4% CH4). The thickness of material deposited was 190 m in the first growth run, and
330 m in the second. Before deposition took place
in the second run, a high-power pure hydrogen plasma was applied for 45 minutes. This step is necessary to clean and prepare the surface prior to growth.
Figure 2 shows the schematics of the growth layers
(left) and DiamondView images (right) taken from
the cross-sectional {100} side of the sample. The
HPHT-grown substrate was subsequently removed
by laser cutting. After polishing, the final thickness
of the sample was about 465 m and the lateral
dimensions were 4.49 4.52 mm.
Sample B was grown for cathodoluminescence
(CL) study under similar conditions. The initial lateral dimensions before laser cutting were 4.32 4.32
mm. Three CVD layers were grown with thicknesses of 190, 175, and 220 m, corresponding to two
growth interruptions resulting in a final thickness of
585 m. Before the growth was resumed, the crystal
was submitted to H2/O2 (98%/2%) etching in highpower conditions for about 30 minutes. This
ensured the surface was clean prior to growth, but it
also induced a slight roughening. To access the phosphorescent region of the sample, a cross-sectional
slice was prepared by laser cutting and polishing
along two opposite corners. The schematics of the
cross-sectional slice of sample B are illustrated in figure 3 (left). The corresponding DiamondView (center) and CL (right) images show the interfaces
between the successive synthetic diamond layers.
Sample A was examined by optical microscopy
combined with luminescence spectroscopy and
imaging techniques. Optical micrographs were
recorded using the D-Scope stereomicroscope. This
microscope (with magnifications of 0.740) was
equipped with an illumination system consisting of
Figure 1. Colorless gem-quality CVD-grown synthetic diamonds such as these (0.220.31 ct) are now
commercially available, making proper identification important. Photo by Robert Weldon.
darkfield, overhead daylight, and fluorescence

modes. A specially designed vacuum sample manipulator allowed easy handling. Crossed-polarized
images were acquired with a Leica DFC digital camera attached to a Leica DL LM microscope.
Luminescence patterns generated by the intense
ultra short-wave UV illumination of the DiamondView instrument were recorded with the maximum
illumination power (100%), full aperture (100%), and
integration times of 410 seconds.
Photoluminescence (PL) measurements were performed on sample A using a Renishaw inVia Raman
microscope at 77 K. The system was equipped with
an Ar-ion laser operating at an excitation wavelength of 514.5 nm. Highly localized PL information
was acquired using a Leica Fluotar L 50 objective
(NA = 0.55) in the high-confocal mode using a 2D
increment of 5 m depth 25 m across, with a slit
width of 20 m and a CCD area of 2 pixels (image
Figure 2. The schematics

of the growth layers in
sample A are shown for a
cross-section across {100}.
At right, the DiamondView luminescence (top)
and phosphorescence
(bottom) images show the
two CVD layers and the
HPHT-grown substrate.
GEMS & GEMOLOGY
FALL 2011
203
Figure 3. The schematics of the growth layers in sample B are also shown for a cross-sectional slice (across {100},
left). The DiamondView luminescence image (center) shows the successive CVD layers and the HPHT-grown
substrate. The cathodoluminescence image (right) depicts the roughened interface between the CVD layers,
which exhibits typical etching features and dark lines due to threading dislocations (Tallaire et al., 2011).
height) 576 pixels (spectrometer range), resulting in

an axial resolution of ~5 m. Applying an automated
xyz sample stage, we recorded detailed line and
depth profiles and 2D mapping.
CL imaging of sample B was performed using a
10 kV electron beam produced in a JEOL 7001F scanning electron microscope. Monochromatic CL
images were taken by filtering the excitonic signal
through the monochromator, which was also
equipped with a photomultiplier detector synchronized with the beam scanning.

Optical Microscopy and DiamondView Imaging.
Strain-related birefringence in sample A is shown in
figure 4 (top left). Typical four-petal patterns related
to dislocation bundles also were clearly observed.
Their density was higher at the boundary with the
HPHT-grown substrate, but they were also visible
throughout the interior of the sample. Two examples of dislocation bundles are indicated with white
arrows. Such threading dislocations in CVD synthetic diamond are usually formed at the substrate/layer
interface and penetrate through the overgrowth by
propagating along the [001] growth direction (Friel et
al., 2009; Pinto and Jones, 2009).
The DiamondView images in figure 4 were taken
from the top (growth side; upper right) and from the
bottom (substrate side; lower left) of sample A, and
showed a blue to blue-green picture frame corresponding to the interface between the subsequent
CVD layers but also above the substrate imprint. In
addition to the picture frame, numerous sharp violetish blue linear features were observed; these are
related to the dislocation bundles.
From the substrate side, sample A also showed a
weak-to-strong red luminescence. This red luminescence originates from NV 0 and NV centers at 575
204
and 637 nm and is characteristic of trace nitrogen

incorporation in this particular region of the sample.
Previous measurements have shown that when no
nitrogen is intentionally added to the gas phase, the
NEED TO KNOW
Production of large single-crystal CVD synthetic
diamonds typically involves multiple growth runs.
Blue to blue-green luminescent zones may be
created when the growth run is interrupted and
resumed.
DiamondView, photoluminescence, and
cathodoluminescence imaging were applied to
study the origin and nature of these luminescent
zones.
Both silicon and boron showed preferential
incorporation at the interface between CVD layers, though the exact cause of the luminescence
is still under investigation.
nitrogen content in the synthetic diamond crystal is

below 10 ppb (Tallaire et al., 2006), which is believed
to be the case here. The incorporation of nitrogen
impurities in the crystal was not uniform, however,
since no red luminescence was observed on the
other side of the sample.
Blue to blue-green phosphorescence lasting up to
several seconds was observed (figure 4; lower right).
Similar phosphorescence has been documented in
HPHT-grown synthetic and treated blue type IIb diamond crystals (Watanabe et al., 1997; Lu and EatonMagaa, 2009). Boron-doped blue type IIb synthetic
diamonds exhibit a blue to blue-green phosphores-
GEMS & GEMOLOGY
FALL 2011
cence peak with a maximum at ~500 nm. In contrast, virtually all natural blue type IIb gem diamonds exhibit two phosphorescence peaks, one at
~500 nm (blue-green) and the other at ~660 nm
(orange-red). In addition, it was reported that an
HPHT-treated blue diamond only exhibited a peak
at 500 nm (Eaton-Magana et al., 2008). These results
suggest that phosphorescence spectroscopy might be
an effective tool for discriminating synthetic from
natural blue diamonds. In this study we report for
the first time the observation of this blue to bluegreen phosphorescence in (near-)colorless CVD synthetic diamond crystals where boron is present as a
background impurity, as no boron was intentionally
added during the growth process.
The origin of this phosphorescence has been
attributed to the generally accepted donor-acceptor
recombination mechanism (Dean et al., 1965), where
holes bound to boron acceptors recombine with electrons that are bound to donors and emit luminescence with energy equal to the difference in energy
between the donor and acceptor. The identity of the
donor impurities is still under debate.
Cathodoluminescence Imaging. As shown in figure
3 (right), the interface between two successive CVD
layers was clearly visible with CL imaging. The

interface was slightly roughened and showed the
appearance of typical etching features.
CL spectroscopy of sample B was performed in a
previous study (Tallaire et al., 2011), and clearly
showed the presence of boron impurities. However,
it was not possible to draw conclusions about nitrogen incorporation from the CL observations.
Photoluminescence Spectroscopy and Imaging. The
normalized PL emission intensity profiles of selected
optical defects (NV0 at 575.0 nm, NV at 637.2 nm,
and a [Si-V] doublet at 736.6736.9 nm) on the substrate side are shown in figure 5 (right). The analyzed
area is marked with an arrow in the DiamondView
image in figure 5 (left). The NV luminescence
decreased progressively from the edge of the layer
toward the interior. The most striking feature was a
sharp increase in the [Si-V] doublet emission near
the blue luminescence band. (Note: Features in the
PL line scan do not reflect the strong red/orange
band visible in the DiamondView image. PL measurements in the confocal mode used in this study
analyze a restricted volume, and the data in figure 5
were obtained from the near-surface. Based on PL
depth profile measurements [see below], there is a
Figure 4. Strain-related birefringence (top

left) was observed between crossed polarizing filters in sample A. The substrates
imprint is indicated (white square), as are
two examples of dislocation bundles
(arrows). In DiamondView images of the
growth side (top right) and the substrate
side (bottom left), a square picture
frame corresponds to the interface
between the subsequent CVD layers. The
dark circular outline indicates the position
of the vacuum sample manipulator. The
corresponding phosphorescence image of
sample A (bottom right) was recorded
with a delay time of 1 millisecond. The
picture frame is clearly presented in the
phosphorescence image.
GEMS & GEMOLOGY
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205
PHOTOLUMINESCENCE INTENSITY PROFILES
NORMALIZED INTENSITY
1.0
0.8
[Si-V]/Raman
0.6
0.4
NV/Raman
0.2
NV0/Raman
0
0
200
400
600
800
1000
LENGTH (m)
Figure 5. DiamondView imaging (left) and normalized photoluminescence intensity profiles (right) of NV0 (575.0 nm),
NV (637.2 nm), and [Si-V] (736.6736.9 nm) from the substrate side of sample A show a decrease in NV luminescence
from the edge to the interior, and a sharp increase in the [Si-V] doublet emission near the blue luminescence band.
great amount of NV luminescence centers present at

depth. Also, the DiamondView image shows both
fluorescence and phosphorescence; the blue to bluegreen phosphorescence is much stronger and overwhelms the red-orange fluorescence.)
A combination of line and depth profiles generates 2D images reflecting the PL intensity of the diamond Raman line and the luminescence associated
with the NV0, NV, and [Si-V] centers, as shown in
figure 6. The [Si-V] associated luminescence is clearly localized in a well-defined zone, and extends vertically over several tens of micrometers. Its location is
consistent with the interface between the two CVD
layers, suggesting preferential incorporation, as with
boron. In contrast, nitrogen does not show clearly
preferential incorporation.
Boron, one of the main impurities reported to
cause phosphorescence, was clearly detected in both
samples (see also Tallaire et al., 2011). In addition,

silicon was found to be incorporated at the interrupted interface where new dislocations were formed.
Although NV centers were absent, nitrogen could
still be present as isolated single substitutional
impurities not causing direct luminescence. The
cause of the phosphorescence at the growth interruption cannot be fully determined at this time, and further studies will be required to identify the contribution of silicon, nitrogen, and dislocations.
CONCLUSIONS
Analysis using complementary luminescence spectroscopy and imaging techniques identified preferential incorporation of trace impurities in the CVD
synthetic diamond crystals, especially at the interface between successive layers. CL analysis confirmed that boron is present at the interrupted inter-
Figure 6. Photoluminescence depth profiles of

the substrate side of sample B were used to create
the two-dimensional maps
on the right, which reflect
the PL intensities of the
Raman line and NV 0,
NV , and [Si-V] centers.
The [Si-V] luminescence
is clearly localized along
the interface between the
two growth layers.
206
GEMS & GEMOLOGY
FALL 2011
face, while PL showed the presence of silicon-related

defects. All these impurities are present at background levels in the CVD reactor chamber. We propose that the uptake of these impurities is enhanced
at the growth resumption of the crystal, leading to
the appearance of a distinct luminescent pattern. On
the microscopic level, the surface is roughened by
the formation of etch pits that decorate threading
dislocations. The surface roughening enhances the
uptake of these impurities and also the generation of
new threading dislocations.
The samples in this study were too thin to be cut
into gemstones, but larger samples are technologically feasible. It is likely that CVD growth techniques
will continue to improve, resulting in purer and larger CVD synthetic diamonds entering the gem market. The spatial distribution of spectroscopic features
is important for CVD synthetic diamond identification, as they can provide evidence of the growth history and, in particular, growth interruptions that are
commonly used for the synthesis of large crystals.
Moreover, typical luminescence features associated
with CVD synthetic diamonds (such as NV 0, NV ,
and [Si-V]), as reported in the literature (Martineau et
al., 2004), were also clearly detected in this study.
The identification of CVD synthetic diamonds
depends on a combination of various gemological

and spectroscopic features, as no single feature will
ensure proper identification. The observations
obtained in this study by DiamondView, cathodoluminescence, and photoluminescence spectroscopy
and imaging showed typical CVD-related optical
centers. The discrete growth interruptions between
subsequent CVD layers can be monitored and visualized. As such, the observations unambiguously
confirmed the synthetic origin of these samples. The
combination of these techniques is fully applicable
in the detection and identification of natural and
synthetic gem diamonds.
ABOUT THE AUTHORS

Dr. Willems (bert.willems@hrdantwerp.be) is a research
scientist in the Research department of HRD Antwerp,
Belgium. Dr. Tallaire is a research associate at Centre
National de la Recherche Scientifique (CNRS), within the
Laboratoire des Sciences des Procds et des
Matriaux (LSPM), Villetaneuse, France. Dr. Barjon is a
lecturer at the Universit de Versailles Saint-Quentin en
Yvelines (Groupe dEtude de la Matire Condense,
GEMaC), Meudon, France.
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Achard J., Tallaire A., Sussmann R., Silva F., Gicquel A. (2005) The
control of growth parameters in the synthesis of high-quality
single crystalline diamond by CVD. Journal of Crystal Growth,
Vol. 284, pp. 396 405, http://dx.doi.org/10.1016/j.jcrysgro.
2005.07.046.
Collins A.T. (1992) The characterization of point defects in diamond by luminescence spectroscopy. Diamond and Related
Materials, Vol. 1, pp. 457469, http://dx.doi.org/10.1016/09259635(92)90146-F.
Dean P.J., Lightowelers E.C., Wight D.R. (1965) Intrinsic and
extrinsic recombination from natural and synthetic aluminum-doped diamond. Physical Review, Vol. 140, No. 1A,
pp. A352A368, http://dx.doi.org/10.1103/PhysRev.140.A352.
Denisenko A., Kohn E. (2005) Diamond power devices. Concepts
and limits. Diamond and Related Materials, Vol. 14, No. 37,
pp. 491498, http://dx.doi.org/10.1016/j.diamond.2004.12.043.
Eaton-Magaa S., Post J.E., Heaney P.J., Freitas J., Klein P.,
Walters R., Butler J.E. (2008) Using phosphorescence as a fingerprint for the Hope and other blue diamonds. Geology, Vol.
36, pp. 8386, http://dx.doi.org/10.1130/G24170A.1.
Friel I., Clewes S.L., Dhillon H.K., Perkins N., Twitchen D.J.,
Scarsbrook G.A. (2009) Control of surface and bulk crystalline
quality in single crystal diamond grown by chemical vapour
deposition. Diamond and Related Materials, Vol. 18, pp.
808815, http://dx.doi.org/10.1016/j.diamond.2009.01.013.
Ho S.S., Yan C.S, Liu Z., Mao H.K., Hemley R.J. (2006) Prospects
for large single crystal CVD diamond. Industrial Diamond
Review, Vol. 66, pp. 2832.
Kone S., Civrac G., Schneider H., Isoird K., Issaoui R., Achard J.,
Gicquel A. (2010) CVD diamond Schottky barrier diode, carrying out and characterization. Diamond and Related Materials,
Vol. 19, pp. 792795, http://dx.doi.org/10.1016/j.diamond.

2010.01.036.
Lu R., Eaton-Magaa S. (2009) Lab Notes: Fancy Intense blue type
IIb synthetic diamond. G&G, Vol. 45, No. 4, pp. 291292,
Martineau P.M., Lawson S.L., Taylor A.J., Quinn S.J., Evans D.J.F.,
Crowder M.J. (2004) Identification of synthetic diamond grown
using chemical vapor deposition. G&G, Vol. 40, No. 1, pp.
225, http://dx.doi.org/10.5741/GEMS.40.1.2.
Pinto H., Jones R. (2009) Theory of the birefringence due to dislocations in single crystal CVD diamond. Journal of Physics:
Condensed Matter, Vol. 21, Art. 364220 (7 pp.), http://dx.doi.
org/10.1088/0953-8984/21/36/364220.
Tallaire A., Collins A.T., Charles D., Achard J., Sussmann R.,
Gicquel A., Newton M.E., Edmonds A.M., Cruddace R.J. (2006)
Characterisation of high-quality thick single-crystal diamond
grown by CVD with a low nitrogen addition. Diamond and
Related Materials, Vol. 15, pp. 17001707, http://dx.doi.org/
10.1016/j.diamond.2006.02.005.
Tallaire A., Barjon J., Brinza O., Achard J., Silva F., Mille V.,
Issaoui R., Tardieu A., Gicquel A. (2011) Dislocations and
impurities from etch-pits at the epitaxial growth resumption
of diamond. Diamond and Related Materials, Vol. 20, pp.
875881, http://dx.doi.org/10.1016/j.diamond.2011.04.015.
Walker J. (1979) Optical absorption and luminescence in diamond. Reports of Progress in Physics, Vol. 42, pp. 16051659,
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Watanabe K., Lawson S.C., Isoya J., Kanda H., Sato Y. (1997)
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GEMS & GEMOLOGY
FALL 2011
207
IDENTIFICATION OF EXTRATERRESTRIAL
PERIDOT BY TRACE ELEMENTS
Andy H. Shen, John I. Koivula, and James E. Shigley
Twenty-six peridot samples from the Esquel pallasite meteorite and 27 samples from 10 terrestrial sources were studied by laser ablationinductively coupled plasmamass spectrometry (LAICP-MS). Among the 32 elements analyzed, six
of themLi, V, Mn, Co, Ni, and Znprovided
an excellent separation between pallasitic and
terrestrial peridot.
eridot, known by the ancient Egyptians as

the gem of the sun, has long been valued as
a gemstone. It was mined on Zabargad (now
St. Johns Island) in the Red Sea some 3,500 years
ago, making it one of the earliest known gemstones
(Gbelin, 1981; Ogden, 1992). Peridot is the gemquality green variety of olivine, an important mineral found in ultramafic igneous rocks such as
dunite and in mafic rocks such as basalt. Among
the major modern productive localities, the main
sources of peridot are peridotite xenoliths in alkali
basalts (U.S., Myanmar, China) and serpentinized
dunites (Pakistan).
Olivine is believed to be one of the major minerals in the earths mantle and in many rocky planets
and smaller bodies in the solar system. Pallasite is a

http://dx.doi.org/10.5741.GEMS.47.3.208.
208
rare type of stony iron meteorite that contains gemquality crystalline olivine in an iron-nickel matrix
(figure 1). It is believed to have formed in asteroids
composed of an iron-nickel core and a silicate mantle (Dodd, 1981). The olivine crystals can be extracted from some of these meteorites to make beautifulalthough typically smallfaceted gems (Koivula et al., 1993a,b, 1994). Pallasitic peridot gemstones
were first characterized in 1991, and the subsequent
report by Sinkankas et al. (1992) found that their
optical and physical properties, such as refractive
index and specific gravity, were very similar to and
overlapped those of their terrestrial counterparts,
negating any useful separation through standard
gemological testing.
Nevertheless, the inclusion suites of pallasitic
peridot can be quite telling, allowing relatively easy
separation from terrestrial material (e.g., Koivula,
1981; Koivula and Fryer, 1986; Milisenda et al.,
1996; figures 2 and 3) by means of magnification. In
addition, due to pallasites fiery descent through
earths atmosphere, inclusion-free extraterrestrial
olivine of significant size (>1 ct) is virtually unheard
of. Olivine is generally heat- and impact-sensitive
and is prone to cracking, so any peridot pieces
extracted from such meteorites are typically fractured, and any gems fashioned from them usually
weigh less than half a carat.
Because pallasitic peridot is a commercially available extraterrestrial gem, there is sufficient interest
to make its identification worthwhile. A peridot
without diagnostic inclusion features requires chemical analysis to make the determination. We used
LA-ICP-MS to study the trace-element chemistry
because of the wide range of elements this technique
can analyze, as well as its superior sensitivity.
GEMS & GEMOLOGY
FALL 2011
Figure 1. These polished pallasitic peridot specimens (50.00 and 25.66 ct) are from the Esquel meteorite, which
was found in Argentina in 1951. Photo by Maha Smith.
In terms of chemical composition, olivine is

among the most extensively studied minerals, with
scores of published studies on major and trace-element chemistry of samples from many natural
occurrences. In the GEOROC database maintained
by the Max Planck Institute for Chemistry in Mainz,
Germany (http://georoc.mpch-mainz.gwdg.de/
georoc), more than 40,000 records are dedicated to
olivine. Yet geochemical studies focusing on gemquality peridot are very limited, and not all trace elements are included in GEOROCs data. The gemological literature contains very few papers on pallasitic peridot (see Sinkankas et al., 1992; Pearson,
2009), let alone detailed studies of its trace-element
composition. To our knowledge, though much
research has been published on the trace-element
composition of olivine in pallasite (see Hsu, 2003
and the references therein), most of the literature is
focused on deducing the parent body or the thermal
history of the pallasites, and very few articles have
mentioned terrestrial olivine at all. One recent study
(Leelawatanasuk et al., 2011) specifically focused on
comparing gem peridots from terrestrial and extra-
terrestrial sources, though using EDXRF rather than

LA-ICP-MS. In this article, we present our chemical analysis results comparing pallasitic peridots to
Figure 2. Cruciform acicular dislocations have been
observed in pallasitic peridot. Such features have not
been seen in terrestrial material. Photomicrograph by
J. I. Koivula; magnified 15.
GEMS & GEMOLOGY
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209
Figure 3. Other internal features distinctive of pallasitic peridot are striated brownish red plates (left) and thin transparent reddish brown platy inclusions (center); the platy inclusions also showed iridescence (right). Neither type of
inclusion could be identified with Raman analysis. Photomicrographs by J. I. Koivula; magnified 80 (left) and field
of view 1.2 mm (center and right).
natural samples from several known terrestrial

localities.

Twenty-six samples of pallasitic peridot and 27 terrestrial samples were examined as part of this study.
The latter consisted of 22 pieces of rough, four
faceted stones, and one cabochon (table 1). Three of
the pallasitic peridot samples were faceted stones,
but the remainder were still in matrix as part of
three polished slabs from the Esquel meteorite (e.g.,
figure 1).
We performed chemical analyses with a Thermo
X Series II ICP-MS. A New Wave Research UP-213
laser ablation unit with a frequency-quintupled
Nd:YAG laser (213 nm wavelength) running at 4 ns
pulse width was chosen to ablate the samples. We

used 55 m diameter laser spots, a fluence of around
10 J/cm2, and a 7 Hz repetition rate. For most of the
terrestrial samples, we selected three spots for
analysis, though some of the rough was tested on up
to six spots. The faceted pallasitic samples received
three analysis spots and the pieces in the slabs only
two. For the ICP operations, the forward power was
set at 1300 W and the typical nebulizer gas flow was
~0.90 l/min. The carrier gas used in the laser ablation unit was He, set at 0.78 l/min. The actual nebulizer flow rate varied somewhat from run to run.
The criteria for the alignment and tuning sequence
were to maximize Be counts and keep the ThO/Th
ratio below 2%. We used National Institute of
Standards and Technology SRM (standard reference
TABLE 1. Terrestrial peridot samples used in this study.

No. samples
Weight (ct)
Description
Sourcea
China
2.984.51
GIA
Huang and Xu (2010)
Hawaii, USA
Kilbourne Hole, Texas, USA
1
2
0.48
2.062.88
Emerald and
triangular cut
Rough
Rough
JIK
GIA
San Carlos, Arizona, USA
1.1710.85
GIA, JIK
Mogok, Myanmar
Norway
Pakistan
2
2
3
0.931.90
9.5317.11
0.6415.11
Saudi Arabia
Tanzania
Zabargad (St. Johns Island),
Egypt
4
2
6
1.602.88
2.492.79
2.335.17
Rough and
oval cut
Rough
Oval cut
Rough and
cabochon
Rough
Rough
Rough
Baker et al. (1996)

Bussod and Williams (1991),
Fuhrbach (1992)
Frey and Prinz (1978)
Locality
GIA
GIA
GIA
JR
GIA
LT, JH
References
Webb (1993)
Kostenko et al. (2002)
Kane (2004), Bouilhol et al. (2009)
McGuire (1988), Camp et al. (1992)
Furman (2007)
Kurat et al. (1993), Brooker et al. (2004)
Initials other than GIA refer to authors or those listed in the Acknowledgments.
210
GEMS & GEMOLOGY
FALL 2011
CHEMICAL COMPOSITION
25
20
Terrestrial
V (ppm)
material) 610 and 612 glasses for calibration. We

analyzed three spots apiece on the standards at the
beginning of the experiment; after every four to five
sample runs, three additional spots were measured.
This process allowed us to correct the drift of the
instrument.
To obtain accurate and precise trace-element
chemistry, we selected 29Si as our internal standard.
To determine the accurate concentration of Si, we
used the method developed by Breeding and Shen
(2008), renormalizing each experimental run into a
model molecular formula of (Mg,Fe,Mn,Ni)2SiO4 and
then calculating the Si concentration from that formula. The calculated Si concentrations were used as
internal standard values for experimental runs, and
the concentrations of the other 27 trace elements
were then calculated.
Extraterrestrial
15
10
0
0
10
12
14
16
Li (ppm)
5000
4000
Terrestrial
Extraterrestrial
Ni (ppm)
Table 2 shows the chemical elements that can be

used to separate pallasitic and terrestrial peridot.
Most olivines belong to a complete solid-solution
series between forsterite (Mg2SiO4) and fayalite
(Fe 2SiO 4). Tephroite (Mn 2SiO 4) and Ni-olivine
(Ni2SiO4) have the same olivine structure and can
form a solid solutiontypically in small amounts
with forsterite and fayalite. Most peridot falls toward
the forsterite end of the solid solution. The majorelement composition of our samples is given in table
2 as molar percent forsterite. This limited range of
compositional variation accounts for the restricted
variability of the gemological properties (Phillips and
Griffen, 1981; Deer, et al., 1982).
3000
2000
1000
0
0
500
1000
1500
2000
2500
3000
Mn (ppm)
80
60
TABLE 2. Concentration ranges of diagnostic trace

elements, and gemological properties, of tested peridot
samples.
Element (ppm)
Terrestrial
Li
V
Mn
Co
Ni
Zn
1.1014.5
0.114.46
7721410
84.8147
17704070
9.0467.4
0.210.96
9.1823.4
19202490
4.3719.6
8.53112
5.209.98
Molar fraction
(forsterite%)
SGa
RI (n )a
RI (n )a
RI (n)a
Fo 96.0Fo88.6
Fo90.0 Fo85.5
3.273.36
1.6401.655
1.6571.675
1.6801.693
3.353.40
1.6521.662
1.6701.683
1.6901.703
Extraterrestrial
Zn (ppm)
Terrestrial
Extraterrestrial
40
20
0
0
20
40
60
80
100
120
140
160
Co (ppm)
Figure 4. Chemical plots of vanadium vs. lithium

(top), nickel vs. manganese (middle), and zinc vs.
cobalt (bottom) all show an obvious separation
between the extraterrestrial and terrestrial peridot
groups. The concentration ranges of these elements are listed in table 2.
Values estimated (RI) or calculated (SG) from Deer et al. (1982).
GEMS & GEMOLOGY
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211
Of the 32 elements studied, sixLi, V, Mn, Co,

Ni, and Znwere diagnostic. Figure 4 (top) is a plot
of V vs. Li, which displays an obvious separation
between pallasitic and terrestrial peridot. The same
observations are seen in the plots of Ni vs. Mn (figure 4, middle) and Zn vs. Co (figure 4, bottom). In all
three of these plots, the data points for the samples
of pallasitic and terrestrial origin are clearly segregated. When we compared our extraterrestrial data set
with published pallasitic olivine chemical data, our
Ni, Co, and Mn concentrations agreed with the
results in Hsu (2003) almost perfectly. All but one of
these six elements, Li, can also be determined using
EDXRF, but the concentrations of V in terrestrial
peridot and those of Co and Zn in pallasitic peridot
may be difficult to detect or determine accurately
with EDXRF because they are so low. However, if an
EDXRF instrument can accurately determine Mn
and Ni, then it is possible to perform the separation
based on these two elements alone (Leelawathanasuk et al., 2011).
Although we analyzed a limited number of peridot samples from a single pallasite and various terrestrial sources, each group showed remarkable consistency. Leelawatanasuk et al. (2011) studied four
different pallasite meteorites, and their results also
showed good consistency among those samples. In
addition, our major-element compositional data
agreed well with the chemistry of most pallasitic
olivines (from over 40 fall locations) listed in Wasson
and Choi (2003). This consistency in major-element
chemistry has been noted in the literature.
CONCLUSION
Twenty-six samples of pallasitic peridot and 27 representative samples from 10 world localities were
analyzed by LA-ICP-MS. The results showed that six
ABOUT THE AUTHOR

Dr. Shen (andy.shen@gia.edu) is a research scientist, Mr.
Koivula is analytical microscopist, and Dr. Shigley is distinguished research fellow at GIA in Carlsbad, California.
ACKNOWLEDGMENTS
The authors thank Lisbet Thoresen (Beverly Hills,
212
Figure 5. Though its rarity limits its commercial significance, pallasite can make an attractive gemstone.
This faceted stone (1.12 ct) from the Esquel pallasite
is resting on a polished slab that was cut from the
same meteorite. Courtesy of Robert A. Haag; photo
by Robert Weldon.
elementsLi, V, Mn, Co, Ni, and Znprovided

excellent separation between pallasitic (figure 5) and
terrestrial origin. The collection of additional data on
pallasitic and terrestrial peridot is ongoing.
California), Dr. John Roobol (retired geologist, Saudi

Geological Survey, Saudi Arabia), and Dr. Jim Harrell
(Professor Emeritus, University of Toledo, Ohio) for providing peridot samples from Saudi Arabia and the Egyptian
island of Zabargad. Pallasitic samples were kindly loaned
for photography by Robert A. Haag (The MeteoriteMan,
Tucson, Arizona).
GEMS & GEMOLOGY
FALL 2011
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GEMS & GEMOLOGY
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213
A HISTORY OF DIAMONDS THROUGH PHILATELY:

THE FRANK FRIEDMAN COLLECTION
Stuart D. Overlin
South African jeweler Frank Friedmans collection of diamond-themed stamps and other postal
material offers an illuminating visual record of
diamond history. Comprising approximately
2,000 pieces, these items chronicle diamond formation, the history of mining and manufacturing, and the evolution of a science and an industry built around this remarkable gemstone.
hilately, the collecting of stamps and other

postal material, first became popular with the
introduction of the British penny and twopenny adhesive stamps in 1840. Much of the hobbys
attraction lies in the range of fascinating subjects
that have been documented. Diamonds have
appeared in postage stamps, special cancellation
marks, and postcards issued by numerous countries,
especially those with ties to the industry (figure 1).
The present article reviews one important collection
of such material.
Frank Friedman (figure 2) has spent much of his
life in the South African gem and jewelry industry.
He joined the family enterprise, J. Friedman Jewellers, as an apprentice goldsmith in 1959 and helped
build it into one of the countrys top retailers. In
1985 he established F. Friedman Jewellers, which
was rebranded as Frankli Wild in 1999.
Mr. Friedman began collecting stamps in 1961,
inspired by a jewelry magazine article that described
See end of article for About the Author and Acknowledgments.

214
the hobby as the poor mans way to collect gems

(Fried man, 2007). He joined the Johannes burg
Philatelic Society to learn more and began to acquire
pieces. His collection now totals approximately
2,000 items from more than 36 countries. In addition to stamps, it contains rare postcards, cancellation marks, historical letters, and original artists
renderings of stamp and cancellation designs.
Mr. Friedman has displayed his collection internationally on several occasions. In 1989 it was showcased in the Harry Oppenheimer Museum at the
Israeli Diamond Center in Ramat Gan. In June 1997,
it was the keynote exhibit at the Vicenza Trade Fair
(Weil, 1997). Awards include a gold medal at the
2006 World Philatelic Exhibition in Washington
(Stamp of approval, 2006), a 2008 silver medal at
the World Stamp Championship in Israel, and a large
vermeil medal at the 26th Asian International Stamp
Exhibition (Joburg 2010).
HIGHLIGHTS FROM THE COLLECTION

Selected items from the Friedman collection, arranged
thematically, are described below. These were chosen
for their historical and educational value.
Diamond Origins. The pair of stamps in figure 3
depicts the eruptive emplacement of diamonds on
the earths surface. The 1973 Lesotho stamp provides a cross-section of a diamond-bearing kimberlite pipe. The artists rendering for a 1993 stamp
from the Tongan island of Niuafoou shows an
erupting volcano juxtaposed with diamond crystals
and a polished stone.
History of Prospecting and Mining. Throughout
much of recorded history, India was the worlds sole
diamond source. After alluvial diamonds began to
GEMS & GEMOLOGY
FALL 2011
NEED TO KNOW
Jeweler Frank Friedmans diamond-themed collection of stamps and other postal material contains ~2,000 pieces, representing more than 36
countries.
The pieces date back to the early 19th century
and illustrate diamond formation, the growth of
the global trade, the cutting and polishing processes, important diamonds, and distinguished
scientists.
Figure 1. These diamond-themed stamps issued by

various countries are shown with seven rough crystals (1.2422.32 ct). The diamonds were donated to
GIA by De Beers chairman Ernest Oppenheimer in
1955. Photo by Robert Weldon.
emerge from Brazil in the mid-1700s, the Portuguese

crown controlled the market for the next hundred
years. The Friedman collections earliest cover, an
envelope or postcard sent through the mail system,
is an 1807 specimen with a postmark from the
Brazilian mining town of Diamantina (figure 4).
The discovery of diamonds in South Africa in late
1866 marked the birth of the modern industry.
Although the country did not issue stamps featuring
diamonds until 1960, other postal items show early
South African mining. Examples are an 1873 cover
with a De Beers NR (New Rush) cancellation mark
and turn-of-the-century postcards from the Jagersfontein and Kimberley mines (again, see figure 4).
Figure 2. Jeweler Frank Friedman examines some of the

prized stamps from his collection. Through stamps
you learn so much about the different countries and
glean a lot of information about the diamond trade in
those countries, he says. Photo by Merle Friedman.
Figure 3. The Lesotho stamp on the left and the artists

rendering for a stamp from the Tongan island of
Niuafoou illustrate the process of diamond emplacement in kimberlite.
Twentieth-century mining developments elsewhere in Africa are represented in figure 5. In 1964,

three decades after it began producing diamonds,
Sierra Leone issued the worlds first self-adhesive
stamps, bearing the inscription Land of Iron &
Diamonds. Subsequent stamps featuring diamonds
GEMS & GEMOLOGY
FALL 2011
215
Figure 4. Early diamond mining history is shown in this series:

an 1807 Brazilian postmark from Diamantina, an 1873 De
Beers NR (New Rush) cancellation, a 1903 postcard of miners
having breakfast at Jagersfontein, and a turn- of-the-century
postcard that features Cecil Rhodes and a washing plant at the
Kimberley mine.
had advertisements for Harry Winston on the paper

backing. Other pieces from this set recognize diamond
mining in South-West Africa (now Namibia). An original artists rendering for a 1974 stamp shows marine
mining along the coastline, while a 1983 issue marks
the 75th anniversary of Namibian diamond mining. In
the latter scene, prospectors are literally scratching the
surface of the desert at Kolmanskop (near Lderitz). A
1987 stamp shows Kolmanskop after it was abandoned in 1950, while a 2008 set of four commemorates the countrys diamond mining centennial.
The Global Diamond Industry. Pioneers of the
African diamond industry appear in figure 6, beginning with a 1940 stamp from Southern Rhodesia
(now Zimbabwe) bearing a likeness of De Beers
founder Cecil Rhodes (18531902). A 75th anniversary stamp commemorates August Stauch, the railroad supervisor who secured the prospecting rights
near Lderitz in 1908 after his employees brought
Figure 5. Items related to 20th century diamond mining
include (clockwise from top left) a diamond-shaped
stamp and a Harry Winston advertisement from the
backing of a self-adhesive stamp, both from Sierra
Leone; an original rendering of coastal mining in SouthWest Africa; four stamps marking the 100th anniversary
of diamond mining in South-West Africa (now
Namibia); and a pair of stamps showing the desert mining town of Kolmanskop.
216
GEMS & GEMOLOGY
FALL 2011
Figure 6. Captured in the

top row are early diamond magnates Cecil
Rhodes, August Stauch,
and Ernest Oppenheimer.
The bottom row shows
an Israeli cancellation
mark for the 1956 World
Congress of Diamond
Bourses, a printers proof
of a 1992 Belgian stamp
issued on the Antwerp
Diamond Clubs centennial, and a 1997 German
stamp celebrating IdarObersteins 500 years as
a gem cutting center.
Figure 7. The individual stamps below depict the transformation of rough diamonds. On the left,
clockwise from top left: a sorter examining a crystal, a processing plant in Ivory Coast, the five
stages of diamond cutting, a worker at a diamond polishing wheel, and a pair of Belgian stamps
commemorating Antwerps role as a world diamond cutting center. Diamonds were once routinely
shipped by regular mail, as seen on the right in a 1940 package containing 1,410 carats sent from the
Williamson mine in Tanganyika.
GEMS & GEMOLOGY
FALL 2011
217
the Antwerp Diamond Clubs centennial, and a 1997

German stamp celebrating 500 years of the diamond
and colored stone industry in Idar-Oberstein.
Cutting and Polishing. Figure 7 follows the transformation of diamonds from rough to polished gems,
starting with a signed proof of a 1972 Ivory Coast
stamp of a diamond processing plant. In a 2001
stamp issued by Botswana, a sorter uses her loupe
visor to examine a crystal. A printers proof of an
Ivory Coast stamp from 1972 shows a processing
plant, while a 1970 Botswanan stamp illustrates the
five stages of diamond cutting: rough octahedron,
sawn crystal, fashioned girdle, polished top, and brilliant cut. A signed proof of a 1966 Central African
Republic stamp shows a worker at a polishing
wheel. Belgian-issued stamps from 1960 and 1983
celebrate Antwerps role as a world diamond cutting
center. Diamonds all along the distribution chain
were once routinely shipped by regular mail, as indicated by the parcel carrying 1,410 carats of diamonds
from the Williamson mine in Tanganyika (now
Tanzania) in 1940, the year it opened.
Figure 8. Famous diamonds appear in these items

from the Friedman collection (top to bottom): a 1953
telegram from the Indian parliament regarding ownership of the Koh-i-Noor, a 1971 Soviet stamp depicting the Shah diamond, South African stamps of
Cullinans I and II, and an original artists rendering
for a 1976 stamp of the Lesotho Brown.
him handfuls of shiny stones. A 1983 stamp from

South-West Africa honors Sir Ernest Oppenheimer
(18801957), who led De Beers for 30 years and
established its Central Selling Organisation in 1934.
The collection also offers a glimpse into the diamond trades impact elsewhere. These pieces
include an Israeli cancellation mark created for Tel
Avivs hosting of the 1956 World Congress of
Diamond Bourses, a 1992 Belgian stamp printed for
218
Famous Diamonds. The Friedman collection also

portrays some of the worlds most exceptional diamonds (figure 8). The first is the legendary Koh-iNoor, the ancient Indian diamond that was handed
over to the British Empire in 1850. Evidence of a
postcolonial dispute over the Koh-i-Noor emerges in
a 1953 telegram from the Indian parliament that
mentions the diamonds ownership. A 1971 Soviet
stamp shows the 88.7 ct table-cut Shah, including
the engraved inscriptions. This diamond was offered
by Persian ruler Fath Ali Shah to placate Czar
Nicholas I after the 1829 assassination of a Russian
diplomat (Balfour, 2000). Cullinans I and II, cut from
a 3,106 ct piece of rough discovered at South Africas
Premier mine, became the centerpiece of the Crown
Jewels of England. They are seen in a pair of 1980
South African stamps issued on the 75th anniversary
of the discovery of the rough. Rounding out this
group is a hand-painted proof of a 1976 stamp featuring the Lesotho Brown. This 603.1 ct diamond was
discovered in 1967 and later cut into 18 stones, one
of which was set in an engagement ring for
Jacqueline Kennedy Onassis (Balfour, 2000).
Scientific Breakthroughs. Figure 9 shows a selection
of stamps commemorating scientists who advanced
our understanding of diamonds. A 1980 German
stamp recognizes naturalist Albertus Magnus
GEMS & GEMOLOGY
FALL 2011
formed early experiments on diamond synthesis. In

1991, South Africa issued a stamp in honor of
Alexander Du Toit, the chief geological consultant
to De Beers from 1927 to 1941. Dr. Du Toit mapped
the geology of his native country and produced influential work supporting the continental drift theory,
which asserts that South Africa and South America
were once connected.
CONCLUSION
Fifty years after starting his collection, Mr. Friedman
still adds to it regularly. One of the thrills of collecting is filling that gap that has eluded me for
years, or finding an unusual variety in an unexpected
way, he says. For instance, Ive just acquired a
Namibian stamp of a diamond-barren kimberlite
pipe. It enhances the Namibian content.
Even in the age of digital communication, philately remains a powerful educational medium, a
form of visual history in miniature. The portraits,
scenes, and other information capture illuminating
details and foster greater appreciation of the subject.
Frank Friedmans philatelic collection, which preserves several aspects of diamond history, represents an important contribution to gemologys
scholarship and heritage.
ABOUT THE AUTHOR

Mr. Overlin is associate editor of Gems & Gemology.
Figure 9. These stamps featuring Albertus Magnus,

Antoine Lavoisier, Pierre and Marie Curie, Henri
Moissan (far left in the group illustration), and
Alexander Du Toit recognize pioneers of diamond
research.
(11931280), a medieval writer on diamonds and one

of the first to document the gems extraordinary
hardness. The famed chemist Antoine Lavoisier
(17431794), whose research demonstrated that diamond consists of pure carbon, is featured in a 1943
French stamp. A 1977 stamp issued by the Central
African Republic pays tribute to Marie and Pierre
Curie, who received the 1903 Nobel Prize in physics
for their early studies of radiation and tested its
effects on diamond. Fellow Nobel Prize winner
Henri Moissan, seen in a 1966 Swedish stamp, per-
ACKNOWLEDGMENTS
The author gratefully acknowledges the research assistance of Kathleen Dailey, Gus Pritchett, and Rose Tozer
of GIAs Richard T. Liddicoat Library and Information
Center in Carlsbad. GIAs McKenzie Santimer and Lynn
Viall provided diamonds for photography.
REFERENCES
Balfour I. (2000) Famous Diamonds, 4th ed. Christie, Manson
and Woods Ltd., London, 320 pp.
Friedman F. (2007) Diamonds and philately. The SA Philatelist,
April, pp. 263264.
Stamp of approval (2006) SA Jewellery News, August, p. 55.
Weil A. (1997) Keystone exhibit honours SA jeweler. Diamond
News & SA Jeweller, August, p. 11.
GEMS & GEMOLOGY
FALL 2011
219
G&G
CHALLENGE
WINNERS
This year, hundreds of readers participated in the 2011 GEMS & GEMOLOGY
Challenge. Entries arrived from around the world, as readers tested their
gemological knowledge by answering questions listed in the Spring 2011
issue. Those who earned a score of 75% or better received a GIA Letter of
Completion recognizing their achievement. The participants who scored a
perfect 100% are listed here.
AUSTRALIA Queensland, Elanora: Bert J. Last. Warwick: Elizabeth

Cassidy. Victoria, Ringwood: Paulina Holmer. Western Australia,
Coogee: Helen Judith Haddy. South Australia, Grange: Barbara
Wodecki BELGIUM Flemish Brabant, Brussels: Brigitte Revol
MacDonald. West Flanders, Ruiselede: Lucette Nols. Egenhoven: Guy
Lalous. Hemiksem: Daniel De Maeght CANADA British Columbia,
Delta: Barbara Mui INDONESIA Jakarta: Warli Latumena IRELAND
Galway: Simon Zaletel ITALY Varese, Malnate: Gabriele Tralli.
Naples: Stefano Montemurro. Udine, Tarvisio: Chiara Piussi LITHUANIA Vilnius: Saulius Fokas NETHERLANDS Rotterdam: E. van Velzen NEW
ZEALAND Tauranga: Graeme Petersen. Wellington: Thomas Brent Layton
SPAIN Las Palma De Gran Canaria: Robert Ernst. Valencia: Monika P. Bergel
Becker SWITZERLAND Zurich: Doris C. Gerber, Eva Mettler UNITED KINGDOM Devon, Okehampton: Damian J. Miles USA Arkansas, Greenbrier:
Beverly A. Brannan. California, Anaheim: Nalini Pattni. Carlsbad: Brenda
Harwick, Abba Steinfeld. Hidden Hills: Bradley Partington. Rancho
Cucamonga: Sandy MacLeane. Redwood City: Starla Turner. Connecticut,
Wilton: Susan DiGeorgio. Florida, Clearwater: Tim Schuler. Deland: Sue
Angevine Guess. Longwood: David Hermann. Riverview: Kenneth S. Fee.
Tampa: R. Fred Ingram. Georgia, Roswell: Gary Braun. Hawaii, Makawao:
Alison Fahland. Iowa, West Des Moines: Franklin Herman. Illinois,
Bloomington: William Lyddon. Downers Grove: Sakina Bharani. Indiana, Carmel:
Wendy Wright Feng. Louisiana, Baton Rouge: Cynthia Gestring-Blumberg. Lake
Charles: Cynthia McCown. Massachusetts, Littleton: Jane L. Millard. Millbury:
Bernard M. Stachura. Maryland, Chevy Chase: Andrea R. Blake. Missouri, Saint
Ann: Bruce S. Hoffmann. Minnesota, Minneapolis: Andy Stevens. Montana,
Billings: Onna Stene. New Jersey, Monmouth Beach: Michele Kelley. West
Orange: Jessica M. Craig. Nevada, Las Vegas: Colleen Walsh. Reno: Terence E.
Terras. New York, City Island: Marjorie Kos. Hawthorne: Lorraine Bennett.
Tarrytown: Ronnie Xu. Ohio, Dayton: Michael Williams. Medina: Charles
Perkins. Pennsylvania, State College: Dennis Zwigart. Rhode Island, Rumford:
Sarah Horst. South Carolina, Sumter: James S. Markides. Texas, Amarillo:
Daniel Novak. Livingston: Janet S. Mayou. Virginia, Hampton: Edward A.
Goodman. Washington, Bellevue: Thomas Charles Estervog. Bothell: Kathryn
Howe. Freeland: Warren Carrow. Seattle: Janet Suzanne Holmes. Wisconsin,
Beaver Dam: Thomas G. Wendt. Pulaski: Stephen Kientop.
220
CHALLENGE WINNERS
Answers
See pages 7576 of the Spring
2011 issue for the questions.
1 (a), 2 (b), 3(c), 4 (c), 5 (d),
6 (a), 7 (d), 8 (c), 9 (c), 10
(b), 11 (b), 12 (c), 13 (a), 14
(d), 15 (b), 16 (b), 17 (c), 18
(d), 19 (c), 20 (b), 21 (d), 22
(b), 23 (d), 24 (b), 25 (a)
GEMS & GEMOLOGY
FALL 2011
EDITORS
Thomas M. Moses
Shane F. McClure
Unusually Large CLINOHUMITE

Clinohumite, (Mg,Fe2+)9(SiO4)4(F,OH)2,
is a fairly rare collectors stone with
orangy yellow to brownish orange coloration. Faceted stones typically
weigh <2 ct, but a few much larger
stones have been cut (e.g., 36.56 ct,
see L. Massi, AIGS Bangkok inspects
exceptional clinohumite from Tajikistan, InColor, Summer 2007, pp.
3031). In the present report, we document the properties of an exceptionally large clinohumite weighing 84.23
ct (32.6 24.79 17.77 mm). For
background information on the cutting of this stone, see Y. Zhukov,
ClinohumiteThe mountain fire,
Editors note: All items were written by staff

members of GIA laboratories.
Figure 1. This faceted clinohumite

weighs an impressive 84.23 ct.
InColor, Spring 2011, pp. 4851.

The stone was faceted into a pear
brilliant and was brownish orange (figure 1). Internal features consisted of
numerous two-phase inclusions (fig-
ure 2, left) and fingerprints, as well

as distinct angular brownish orange
growth lines (figure 2, center), as documented previously in clinohumite
(e.g., U. Henn et al., Gem-quality clinohumite from Tajikistan and the
Taymyr region, northern Siberia,
Journal of Gemmology, Vol. 27, No. 6,
2001, pp. 335339; and Winter 2004
GNI, pp. 337338). Abundant twin
planes were also seen with crosspolarized light (figure 2, right). The
stone was inert to long-wave UV radiation, whereas short-wave UV produced moderate orange to strong
chalky yellow fluorescence along the
growth lines. Its Raman spectrum,
along with gemological properties
such as RI (1.6351.670) and SG (3.21)
values, confirmed that it was clinohumite. IR spectroscopy recorded typical
absorptions for clinohumite, including
a broad band centered at 3560 cm1 due
to OH stretching and additional bands
at 4100 and 4510 cm1 caused by
MgOH units and Si-OH bonding,
Figure 2. Microscopic observation of the clinohumite revealed two-phase (fluid-gas) inclusions,

(left, magnified 35), distinct angular brownish orange growth lines (center, 12), and numerous
twin planes (right, cross-polarized light, 75).
222
LAB NOTES
GEMS & GEMOLOGY
FALL 2011
respectively (R. L. Frost et al., Nearinfrared and mid-IR spectroscopy of

selected humite minerals, Vibrational Spectroscopy, Vol. 44, 2007, pp.
154161, http://dx.doi.org/10.1016/
j.vibspec.2006.11.002). The FTIR and
Raman spectra of this stone are available in the G&G Data Depository
(gia.edu/gandg). Energy-dispersive Xray fluorescence (EDXRF) spectroscopy detected major amounts of Mg,
Fe, and Si, and traces of Ti and Mn, as
expected for clinohumite.
There are two main localities that
produce gem-quality clinohumite
the Pamir Mountains of Tajikistan
and the Taymyr region of northern
Siberia (Massi, 2007). Unfortunately,
the geographic origin of the present
clinohumite is unknown. It is the
largest gem-quality clinohumite ever
tested at GIA.
Kyaw Soe Moe and Wai Win
DIAMOND
Black Diamond, Colored by Strong
Plastic Deformation
Black color in diamonds can have various natural or artificial causes, from
inclusions (abundant graphite or pinpoints, or dense clouds) to heating or
extremely strong irradiation. The
New York laboratory recently examined a black diamond colored by
another mechanism.
This round-cut diamond weighed
Figure 3. The black color of this
0.85 ct diamond is attributed to
very strong plastic deformation.
Figure 4. With magnification and

very strong lighting, the diamond
in figure 3 showed a dark brown
color with banded linear distribution. Magnified 70.
0.85 ct (5.70 5.78 3.87 mm) and was
color graded as Fancy black (figure 3).
Viewed with magnification and very
strong fiber-optic illumination, it
revealed fractures and mineral inclusions, as well as a dark brown color
with banded linear distribution (figure
4). Strong plastic deformation and the
related linear banding were also clearly
revealed in the DiamondView. Its midinfrared spectrum showed strong Nrelated absorption in the one-phonon
region and a weak H-related feature at
3107 cm1. Also recorded were very
strong absorptions from amber centers
at ~4170 and 4070 cm1, with intensities of 2.0 and 1.1 cm1, respectively.
The vacancy cluster, a diamond
lattice defect closely related to plastic
deformation, usually absorbs visible
light from ~600 nm to lower wavelengths. When its concentration is
very high, such as in this diamond, its
absorption extends across the entire
visible light region and blocks the vast
majority of light. It is very rare to see a
natural gem diamond with such
strong plastic deformation that it
causes a black appearance. This stone
demonstrates yet another cause of natural black color in diamond.
Wuyi Wang
Figure 5. This 1.29 ct diamond

proved to be coated to enhance
its black color appearance.
2010 Lab Notes sections and S. V. Titkov et al., An investigation into the
cause of color in natural black diamonds from Siberia, Fall 2003, pp.
200209). This color, when natural, is
typically caused by dark/intense mineral or cloud inclusions. It can also be
induced by artificial irradiation or
graphitization along fractures due to
heating (naturally or in the laboratory).
Recently, the New York laboratory
received a 1.29 ct black pear shape (figure 5) for color origin determination.
Infrared absorption spectroscopy confirmed it was a type Ia diamond with
hydrogen impurities. As expected, it
was inert to both long- and short-wave
UV radiation. However, microscopic
examination revealed a distinctly
lighter color along the facet junctions
(figure 6), and these areas showed contrasting luminescence in the
Figure 6. In reflected light, the
1.29 ct diamond displays a distinctly lighter color along the
facet junctions. Magnified 30.
Coated Black Diamond

Gems & Gemology has reported on a
number of interesting black diamonds
in recent years (see the Spring 2007,
Winter 2007, Fall 2008, and Summer
LAB NOTES
GEMS & GEMOLOGY
FALL 2011
223
Figure 7. In the DiamondView, the coating on the black diamond was

apparent from the different luminescence of the facet junctions,
where it had apparently worn off (left). After cleaning with acetone
and corundum powder (with client permission), the coating appeared
smeared and the junctions were less distinct (right).
DiamondView (figure 7). The girdle
also showed uneven concentrations of
dark color, and there were scratches
on the pavilion that were lighter than
the black bodycolor; both of these
could be easily observed with the
microscope. Feathers within the diamond were dark colored due to black
natural inclusions. It was obvious that
this diamond, though rather dark, had
been coated to further enhance its
color.
This was our first encounter with
a coated black diamond. Because of
the coating, we did not issue a color
grade. In this case, the black coating
made the stone appear a deeper, more
even black. Although coating a black
diamond can improve its overall
appearance or color distribution, in
this case the treatment was detectable
with a microscope.
Erica Emerson
Coated Diamond with

Spectroscopic Features of a
Natural-Color Pink
Coated diamonds are fairly commonly
encountered, both in the trade and the
grading lab. Most coatings consist of a
thin film applied to one or more pavilion facets, often at or near the girdle
edge, though sometimes the coating
will completely cover the diamonds
surface. Because of the value of natural-color pink diamonds, pink is a
common choice for such coatings,
which are intended to deepen a weak
bodycolor or to mask an undesired one
(e.g., Winter 2010 Lab Notes, pp.
299300). This treatment can be identified through microscopic observation and UV-Vis spectroscopic features. In the case of pink-coated diamonds, the typical absorption band at
~520 nm (see A. H. Shen et al.,
Figure 8. This 1.05 ct diamond owed its apparent Fancy Light brown-pink
color (left) to a coating. After the coating was removed by acid cleaning,
the diamond was given a color grade of J (right).
224
LAB NOTES
Serenity coated colored diamonds:

Detection and durability, Spring
2007 G&G, pp. 1634, http://dx.doi.
org/10.5741/GEMS.43.1.16) is easily
distinguished from the ~550 nm band
in natural-color stones.
The 1.05 ct heart-shaped diamond
in figure 8, recently submitted for
color grading, initially received a grade
of Fancy Light brown-pink. Its UV-Vis
spectrum showed the broad ~550 nm
absorption band (figure 9) typical of
naturally colored pink diamonds.
With magnification, however, a coating was clearly visible on the pavilion
facets (figure 10). After the coating was
removed by boiling the stone in acid,
the color grade was revised to J (figure
8, right).
Because the normally diagnostic
absorption band for a pink coating
was shifted from 520 to 550 nm,
spectroscopy alone would not have
detected this coating. This reinforces
the essential role of conventional
observation in gem identification.
Sally Chan
Colorless Untreated Diamonds

with High Levels of Strain
Diamonds form under enormous
heat and pressure deep in the earth,
and endure additional stresses during
their journey to the surface. Such
stresses can cause irregularities in
their lattice structure, which can
impart color to a diamond in a variety
of ways. For example, brown color in
type IIa diamonds is believed to be
caused by vacancy clusters, and the
depth of color generally corresponds
to the degree of strain (D. Fisher et al.,
The vacancy as a probe of the strain
in type IIa diamonds, Diamond and
Related Materials, Vol. 15, 2006, pp.
16361642, http://dx.doi.org/10.1016/
j.diamond.2006.01.020; D. Fisher,
Brown diamonds and high pressure
high temperature treatment, Lithos,
Vol. 112S, 2009, pp. 619624, http://
dx.doi.org/10.1016/j.lithos.2009.
03.005). Since high-pressure, hightemperature (HPHT) treatment can
remove brown color from type IIa
diamonds but has a minimal effect
GEMS & GEMOLOGY
FALL 2011
VISIBLE ABSORPTION SPECTRA
ABSORBANCE
0.20
0.15
550
0.10
Coated pink diamond

0.05
Natural pink diamond

0
400
450
500
550
600
650
700
750
WAVELENGTH (nm)
Figure 9. The coated diamonds absorption band at ~550 nm was very
similar to that of a naturally colored pink diamond. Both spectra were
collected at liquid-nitrogen temperature.
on strain, the presence of strain can
be an important criterion for identifying HPHT-annealed stones.
Recently, the Carlsbad laboratory
received two colorless type IIa diamonds for identification: a 0.90 ct Ecolor marquise and a 0.73 ct D-color
round brilliant. Based on gemological
and spectroscopic features, these diamonds were found to be natural and
untreated. However, in the course of
this determination, we also noticed
that both showed an unusually high
degree of tatami strain (figure 11)
when viewed with cross-polarized
Figure 10. A pink coating on the

diamonds pavilion facets was
clearly visible with magnification
(here, 40).
LAB NOTES
light. The strong strain patterns were

more consistent with those seen in
brown diamonds. Typically, type IIa
colorless diamonds show a tatami
pattern, but with a lower concentration of strain laminations.
In addition to visual assessment
using crossed polarizers, an indirect
but relatively reliable indicator of
strain is the peak width of certain
defects determined from photoluminescence (PL) spectra taken at liquid
nitrogen temperature. The PL spectrum of the 0.90 ct diamond showed
both the neutral (575 nm) and negatively charged (637 nm) NV centers;
the full width at half maximum
(FWHM) for these centers was 0.89
and 1.56 nm, respectively. As with
the observed strain, these values were
much higher than is commonly seen
in untreated colorless diamonds. A
compilation of calculated FWHM values for 250 untreated diamonds in the
DE range showed that the NV 0 center had an average width of 0.29 nm
with a standard deviation of 0.07 nm;
the highest value was 0.65 nm. For
the NV center, the average width
was 0.30 nm with a standard deviation of 0.10 nm; the maximum was
0.79 nm. These values are far lower
than those for the 0.90 ct diamond.
It is unusual to find natural-color
diamonds that endured such a high
amount of stress during their history
and yet remained colorless. One possible explanation is that the associated brown coloration was naturally
annealed out during their geologic
history.
Sally Eaton-Magaa
HPHT Treatment for Subtle

Color Enhancement of Diamond
It is well known that HPHT annealing can remove brown coloration
from natural type IIa diamonds, making them colorless to near-colorless.
While a significant number of HPHT-
Figure 11. These untreated natural type IIa diamonds (0.90 ct E color, left;
0.73 ct D color, right) experienced a high amount of stress, as evidenced by
the extensive tatami strain seen in cross-polarized light. They are unusual since they do not show any of the brown color that typically correlates
with such strain. (The apparent brown color in these images is an artifact of
the lighting.)
GEMS & GEMOLOGY
FALL 2011
225
Figure 12. Shown here after HPHT treatment (EF color, 1.742.57 ct),
these type IIa diamonds originally had color grades of JM. This demonstrates that HPHT annealing is being used to make subtle color improvements in such diamonds.
treated type IIa diamonds have been
seen in gem laboratories over the past
decade, little has been published on
the characteristics of the starting
materials. Recently, however, the
New York laboratory had the opportunity to follow four diamonds
through the HPHT treatment process.
When they were first received,
three of the four round diamonds
(1.82.6 ct) were color graded in the
JK range, with the fourth being M
color. Photoluminescence spectroscopy confirmed that they were naturally colored. Infrared spectroscopy
showed they were very pure type IIa;
only one stone had an extremely
weak hydrogen-related absorption, at
3107 cm1. When the diamonds reappeared in the lab very recently, their
color ranged from E to F (figure 12).
They also showed a 25% weight
loss, consistent with the necessary
repolishing after treatment. Their
226
LAB NOTES
photoluminescence spectra revealed

the exact changes that were expected
as a result of HPHT annealing.
Though the general impression of
HPHT treatment in the trade is that it
is used to turn obviously brown diamonds colorless, this experience suggests that such treatment may also be
used to achieve more subtle improvements in diamond color.
Wuyi Wang
the Carlsbad laboratory recently graded a type Ia colorless round brilliant

with a remarkable cleavage-related feature. The cleavage showed prominent
brown radiation staining, suggesting
that radioactive fluids had been present in the post-growth environment
(figure 13). When the diamond was
viewed face-up in the microscope with
darkfield illumination, the cleavage
also exhibited pronounced green luminescence to visible light (figure 14,
left); fiber-optic illumination made the
green luminescence even more dramatic. Radiation stains are well documented in the gemological literature
(e.g., J. I. Koivula, The MicroWorld of
Diamonds, Gemworld International,
Northbrook, Illinois, 2000).
Green luminescence in diamond
is known to be produced by the H3
lattice defect (503.2 nm), which consists of two nitrogen atoms separated
by a vacancy (N-V-N)0. When examined in the DiamondView, the stone
showed clear green fluorescence along
the cleavage (figure 14, right). Using
this image as a map, we collected photoluminescence data from the cleavage area. In addition to the H3 defects,
analysis also revealed high concentrations of the 3H interstitial defect
(503.4 nm). An interstitial defect
occurs when a carbon atom is displaced from its original lattice position, typically by radiation. Thus, the
occurrence of 3H with the green
luminescing H3 defects is consistent
Figure 13. The brown coloration
confined to the cleavage area of
this diamond resulted from the
interaction of radioactive fluids
in the post-growth environment.
Magnified 20.
An Interesting Luminescent
Cleavage in Diamond
Although diamond is the hardest natural substance, it still is susceptible to
breakage along its cleavage directions.
Often mistakenly described as a fracture, cleavage is one of the most common clarity characteristics in gemquality diamonds, and generally is of
little interest to gemologists. However,
GEMS & GEMOLOGY
FALL 2011
of large diamonds can now be treated

successfully, though these can still be
identified by gem labs. This 21.73 ct
pink diamond is one of the largest
HPHT-treated pink diamonds identified in GIAs laboratories.
Wuyi Wang
Figure 14. Darkfield illumination revealed green luminescence along the

cleavage shown in figure 13 (left, see arrows; magnified 20x). In the
DiamondView (right), green luminescence from the H3 defect was clearly visible. Magnified 30.
with the microscopic evidence of
radiation staining.
This is one of the more unusual
examples of cleavage we have seen in
the Carlsbad laboratory. The diamonds cleavage, radiation staining,
and green luminescence all reveal
important information about its history and indicate that radiation exposure occurred naturally.
Nathan Renfro and
Christopher M. Breeding
A Large HPHT-Annealed
Pink Diamond
Unlike irradiation treatment, which
usually adds additional color, annealing a natural diamond under HPHT
Figure 15. This 21.73 ct Light
pink diamond proved to be
HPHT annealed.
LAB NOTES
conditions can remove preexisting

colors as well as create new ones.
When a suitable type IIa brown diamond is HPHT annealed at temperatures appropriate for removing brown
but not pink coloration, then the preexisting pink color can be enhanced.
Such HPHT-treated type IIa pink diamonds have been available for more
than 10 years (e.g., Fall 2000 Lab
Notes, pp. 254255).
The New York laboratory recently
received the large pink diamond in figure 15 for identification. This marquise brilliant (28.15 15.41 7.71
mm) weighed 21.73 ct and was color
graded Light pink. The color was distributed evenly throughout the stone
with no detectable pink graining, and
it showed typical blue fluorescence
when examined in the DiamondView.
The mid-IR spectrum showed type IIa
features with no detectable hydrogenrelated absorption at 3107 cm1. A
weak band centered at ~550 nm was
present in the UV-Vis absorption spectrum at liquid nitrogen temperature.
This band is very common in naturally colored pink-to-red diamonds and
can be made more visible by removing
other unwanted colors. Photoluminescence spectra collected at liquid
nitrogen temperature with varying
laser excitations confirmed that this
diamond was HPHT annealed.
HPHT annealing has become a
very common type of diamond color
treatment. With advances in processing techniques, a substantial number
SYNTHETIC DIAMOND
Gem-Quality CVD Synthetic
Diamonds from Gemesis
In recent years, limited quantities of
gem-quality synthetic diamonds produced by chemical vapor deposition
(CVD) have reached the market. Most
of these have come from Apollo
Diamond Inc. (Boston, Massachusetts).
We recently examined similar products introduced by Florida-based
Gemesis Corp., better known for its
HPHT-grown synthetic diamonds (J. E.
Shigley et al., Gemesis laboratory-created diamonds, Winter 2002 G&G,
pp. 301309). In November 2010, the
company announced plans to market
CVD-grown synthetics.
GIA examined 16 CVD synthetic
diamonds (e.g., figure 16) that were
faceted as round brilliants with the
exception of one rectangular cut.
They ranged from 0.24 to 0.90 ct, with
an average weight of 0.46 ct. They
were colorless (3 samples), near-colorless (11), and lightly colored (2). For
the most part, clarity grades fell
between IF and VVS, due to internal
graining and a few pinpoint inclusions. Only four of the 16 samples had
VS clarity.
Infrared absorption spectroscopy
revealed that all of the CVD synthetic
diamonds were type IIa. Unlike typical
as-grown CVD products, no defectrelated absorptions were recorded in
either the mid- or near-infrared
regions. Photoluminescence analysis
of all samples showed moderately
strong emission from the H3 optical
center (zero-phonon line at 503.2 nm),
moderately strong emissions from NV
centers (575.0 and 637.0 nm), and moderate to strong emissions from the [SiV] center (doublet at 736.6 and 736.9
GEMS & GEMOLOGY
FALL 2011
227
Figure 16. These CVD synthetic diamonds were produced by Gemesis.

The 0.39 ct round brilliant on the left was graded F color and VVS2
clarity; the 0.83 ct sample on the right was graded J-VVS2.
nm). In four samples, the [Si-V] concentrations were relatively high and
could even be detected in the UV-Vis
absorption spectra. A notable feature of
these synthetic diamonds was their
weak to moderate green fluorescence
to short-wave UV radiation. Most were
inert to long-wave UV radiation, with
only five samples showing very weak
green fluorescence. In the DiamondView, they exhibited strong green fluorescence and noticeable blue phosphorescence; characteristic growth striations also were easily seen.
Gemological and spectroscopic
observations strongly suggested that
these CVD synthetic diamonds were
annealed after their growth, presumably to improve their color and transparency. This study confirms that
the quality of CVD synthetic diamonds continues to improve. Nevertheless, gemological and spectroscopic features can clearly separate
Gemesis CVD synthetics from natural diamonds.
Wuyi Wang and Thomas M. Moses
the past few years (see, e.g., Lab Notes:

Winter 2005, pp. 341343; Spring
2010, pp. 5152 and 5254; and
Winter 2010, pp. 300301). Two more
examples recently submitted (on sepa-
rate occasions) to the New York laboratory showed an unusual fluorescence effect.
The two round brilliants (0.47 and
0.63 ct; figure 17) were color graded
Fancy Vivid purplish pink and Fancy
Deep purple-pink, respectively. Their
mid-IR spectra indicated they were
type Ib, with a very low concentration of isolated nitrogen. However,
they did not display the tatami
strain pattern expected for such
diamonds, so we tested them using
the DiamondView. The 0.47 ct
round brilliant showed the cuboctahedral pattern typical of HPHT synthetic growth, while the 0.63 ct sample had a CVD growth pattern; both
displayed strong orange luminescence (figure 17, bottom). Microscopic examination revealed strong
color zoning along growth sectors in
the 0.47 ct synthetic, but this effect
was very subtle in the 0.63 ct sample
Figure 17. These treated-color synthetic diamonds (0.47 and 0.63 ct) have
an evenly distributed face-up color. Their DiamondView images (bottom)
display the patterns typical of HPHT (left) and CVD growth (right).
Treated Synthetic Diamonds with

Pink Color Intensified by
Fluorescence
A combination of irradiation and
HPHT annealing can create pink to
red colors in both natural and synthetic diamonds. We have reported on a
number of these treated stones over
228
LAB NOTES
GEMS & GEMOLOGY
FALL 2011
NV centers, due to their much lower

concentrations.
Kyaw Soe Moe
PEARL
Cultured Pearls from Pteria Sterna
With Plastic Bead Nuclei
It is generally agreed that freshwater
mother-of-pearl shell nuclei produce
the best results for both saltwater and
freshwater beaded cultured pearls.
Occasionally, other materials such as
saltwater shell, ceramic, plastic, or
wax have been used, but these are not
common due to high rejection and
mortality rates (P. C. Southgate and J.
S. Lucas, Eds., The Pearl Oyster, Elsevier, Amsterdam, 2008).
Recently, we received two yellowish brown samples (both ~8 mm in
diameter; e.g., figure 20) for identification. Microradiography revealed centrally positioned beads that were
noticeably more transparent to X-rays
than typical freshwater shell nuclei.
The beads appeared to have distinct
Figure 18. In diffused light, the 0.47 ct pink synthetic diamond displayed
strong, uneven color zoning along growth sectors (left, magnified 45).
The 0.63 ct sample only showed subtle color zoning (right, 35).
LAB NOTES
smooth, gentle slope (indicated by

the blue dotted line in figure 19).
These samples had a more pronounced window (represented by the
shaded region) due to the emission
from NV centers. Fluorescence from
the NV center, activated by visible
light, strongly enhances pink to red
color in diamond. This phenomenon
is not as obvious in natural-color
pink diamonds that are colored by
Figure 19. In this UV-Vis-NIR absorption spectrum (here, of the 0.47 ct sample), the unusual shaded region represents the strong emission of NV centers, which contribute to the pink bodycolor. In most natural-color pink
diamonds, this region normally shows the absorption indicated by the blue
dotted line.
UV-VIS-NIR ABSORPTION SPECTRUM
595
575
637
ABSORBANCE
(figure 18). The former had only a

VVS1-grade feather in the lower girdle facet, while the latter contained
graphitized feathers and tiny black
particles (possibly graphite).
The diamonds UV-Vis-NIR absorption spectra were collected at liquid-nitrogen temperature with broadband illumination (Avantes AvaLightHAL-S) and a CCD detector (Ocean
Optics HR-4000). This light source
has significant emission in the visible-light region (>400 nm) but very
little in the UV region. The 575 nm
feature (zero-phonon line of NV 0)
appeared as a negative peak (figure
19), caused by fluorescence. Strong
fluorescence was also present in the
~650825 nm region from the NV
center (637 nm). In addition, a sharp
peak at 595 nm was recorded in the
absorption spectra, and this peak,
together with the strong NV features
at 575 and 637 nm, were also detected
in low-temperature photoluminescence spectra. These features suggest
that both pink synthetic diamonds
had undergone post-growth treatments, such as irradiation and annealing. These treatments caused the
vacancies to migrate and combine
with preexisting isolated nitrogen
atoms, forming the NV centers that
produce the strong purplish pink
color.
The absorption spectra of most
pink diamonds that are naturally colored by NV centers show a transmission window in the red region with a
400
500
600
700
800
900
1000
WAVELENGTH (nm)
GEMS & GEMOLOGY
FALL 2011
229
sterna mollusks. Whether this atypical

bead material is becoming more prevalent is unknown.
[Note: Though we have used the
term cultured pearl in this note for
simplicity, we recognize that in this
instance the usage may not be in
agreement with recognized definitions, e.g., the CIBJO Pearl Book.]
Chunhui Zhou and Akira Hyatt
Figure 20. This cultured pearl from Pteria sterna (left, ~8 mm in diameter)
proved to have a plastic bead. X-ray computed microtomography of a
similar sample (center) showed the presence of a near-X-ray-transparent
bead as well as a drill hole. When the first sample was sawn in half
(right), a white plastic bead was revealed inside.
Large Conch Pearl

uniform edges and drill holes, although
the cultured pearls themselves were
not drilled. One had a slight exterior
depression apparently corresponding
to one end of the drill hole.
Further gemological testing (UV
fluorescence, UV-Vis reflectance spectroscopy, and EDXRF analysis) indicated that these samples were from
the saltwater mollusk Pteria sterna, a
species native to the Sea of Cortez in
Mexico. Although we have occasionally seen cultured pearls with near-Xray-transparent beads, and reported on
some of them in the Lab Notes section
(e.g., Summer 1988, pp. 114115;
Spring 1994, p. 45), we decided to
acquire the samples from the client in
order to investigate further and identify the material that was used.
One of the two samples was examined using X-ray computed microtomography to obtain more detailed
images of its internal structure (figure
20, center). The resulting images confirmed, with more detail, a distinct
uniform bead outline and drill hole.
The second sample was cut in half for
visual observation and Raman spectroscopic analysis. The exposed bead was
semitranslucent, white, with a plasticlike appearance (figure 20, right), and
was easily scratched using a metal
probe. Raman spectroscopy showed a
dominant peak at 997 cm1, which corresponded to predominantly aromatic
functional groups of possible polystyrene materials.
This is the first time we have
reported on plastic beads used in Pteria
Figure 21. The very large conch pearl in the pendant weighs approximately 100 ct. By comparison, most conch pearls (left, 8.04 ct, 13.53 10.65
7.95 mm) are much smaller, as are South Sea (second from right, 13.00
mm) and akoya cultured pearls (right, 6.75 mm).
Pearls from the Queen conch, Strombus gigas, have long been collectors
items, prized for their unique and
attractive color and surface structure.
Conch pearls come in a range of colors from white to yellow to brown,
but the most desirable is pink.
Recently, a large conch pearl
mounted in a pendant (figure 21) was
submitted to the New York laboratory
for identification. The baroque-shaped
light pink to white specimen measured
35.20 21.65 16.33 mm, weighed
approximately 100 ct, and showed a
very fine flame structure (figure 22). Xradiography revealed an unusually
large number of layered natural growth
structures, which corresponded to the
contours of the pearls surface.
Raman and UV-Vis reflectance
spectra were collected from both the
light pink and white regions of the
pearl. Raman spectroscopy of the pink
area with 514 nm excitation showed
two small peaks at 1520 and 1130 cm1,
which are characteristic of the pigments responsible for pink color in
Figure 22. The large conch pearl
in figure 21 displayed a very fine
flame structure. Magnified 100.
230
LAB NOTES
GEMS & GEMOLOGY
FALL 2011
conch pearls. These peaks were barely

visible in the spectrum of the white
area. The UV-Vis reflectance spectrum
of the pink area also showed stronger
absorption between 480 and 560 nm
than did that of the white area; this
absorption in the green region of the
spectrum is responsible for the pink
color. All of these results suggested
that the pink color was natural and not
the result of treatment.
Though most conch pearls are
small (see E. Fritsch and E. B. Misiorowski, The history and gemology
of Queen conch pearls, Winter
1987 G&G, pp. 208221), large ones
have been reported. The 2005
Allure of Pearls exhibit at the
Smithsonian Museum of Natural
History (www.mnh.si.edu/exhibits/
Pearls/index2.htm) featured two loose
pink conch pearls belonging to collector Susan Hendrickson that weighed
17.70 and 22.40 ct, as well as the
Queen Mary Brooch set with two pink
conch pearls weighing 24.90 and 28.10
ct. We reported on another large conch
pearl in 2008 (125.26 ct; Spring 2008
Lab Notes, p. 72); though that baroque
specimen was somewhat larger than
this pearl, the bodycolor was a mix of
pink, orange, and white. Most conch
pearls are far smaller (again, see figure
21), making this specimen a true rarity, in both size and quality.
JaeWon Chang and Akira Hyatt
SAPPHIRE
Natural and Synthetic Green
Sapphires with Similar Color but
Remarkably Different Chromophores
indicative of a melt-grown synthetic.

LA-ICP-MS analysis confirmed that it
was synthetic sapphire, as cobalt was
the only trace element detected (average 25 ppma). Previous reports on
cobalt-doped melt-grown synthetic sapphires were published in Spring 1996
Lab Notes (p. 51), Spring 2001 Gem
News International (pp. 7577), and
Spring 2008 Lab Notes (pp. 7273).
Sapphireswhether natural or
syntheticwith such a distinct green
coloration are rarely seen in the lab,
and it is quite interesting that two
very different compositions produced
such a similar coloration. UV-Vis-NIR
spectroscopy of the natural sapphire
showed an absorption spectrum typical of corundum with a high iron content: strong lines at 450, 388, and 377
nm from Fe3+, and broad bands at 580
and 700 nm due to Fe2+-Ti4+ intervalence charge transfer (figure 24). In
addition, the 10501075 nm band (due
to Fe3+) was surprisingly strong. It is
well known that a high content of Fe3+
induces a yellow coloration in sapphire, and even small concentrations
of Fe2+-Ti4+ pairs contribute a blue
color component. The resulting green
color of this sapphire, which had an
average Fe content of 1155 ppma, is
quite consistent with its composition.
Polarized UV-Vis-NIR spectra of
the synthetic sapphire showed only

two broad bands centered at 450 and
660 nm, which have been attributed
to Co 3+ substituting for octahedral
Al 3+ (e.g., R. Mller and Hs. H. Gnthard, Spectroscopic study of the
reduction of nickel and cobalt ions in
sapphire, Journal of Chemical
Physics, Vol. 44, No. 1, 1966, pp.
365373, http://dx.doi.org/10.1063/
1.1726471). The two band positions
were virtually identical for the ordinary and extraordinary rays, but the
intensity of the 660 nm band was
greater for the ordinary ray. Furthermore, a weak sharp line at approximately 691 nm was visible in the
ordinary ray spectrum. A transmission window near 500 nm in the spectra of both samples is largely responsible for their similar green coloration.
Color coordinate calculations
using the spectra reported in Mller
and Gnthard (1966) for 2-mm-thick
wafers gave L*a*b* coordinates of
81/51/20 and 86/34/36 for the ordinary ray and extraordinary ray, respectively (again, see figure 23). These correspond to a coloration that is remarkably similar to the synthetic sapphire
reported here, supporting our conclusion that its color is due to Co3+.
Emily V. Dubinsky
Figure 23. The 12.80-mm-long sapphire on the left was identified as natural, with its color due to a high iron content. The 2.07 ct gem on the right
is a cobalt-bearing synthetic sapphire. For comparison, color coordinates
(far right) were calculated for optical spectra reported in Mller and
Gnthard (1966) for Verneuil synthetic sapphire containing Co 3+
(ordinary ray, top; extraordinary ray, bottom).
Recently, two green gems were submitted to the New York laboratory. One
stone (12.80 10.90 8.75 mm; figure
23, left), mounted in a ring with numerous transparent near-colorless stones,
was easily identified as a natural sapphire by its inclusions and trace-element content measured by LA-ICP-MS.
The other gem (2.07 ct; 7.77 6.09
4.93 mm) had no readily apparent inclusions (figure 23, center). Careful examination of the latter gem in immersion
revealed faint curved color banding,
LAB NOTES
GEMS & GEMOLOGY
FALL 2011
231
UV-VIS-NIR ABSORPTION SPECTRA

4.5
Fe3+
4.0
Natural, mixed ray

Synthetic, ordinary ray
ABSORBANCE
3.5
Synthetic, extraordinary ray
3.0
2.5
2.0
1.5
Fe2+-Ti4+
1.0
Fe3+
0.5
Co3+
0
300
Co3+
500
700
900
1100
1300
WAVELENGTH (nm)
Figure 24. In these UV-Vis-NIR spectra, the natural green sapphire shows
strong Fe-related features that are absent from the synthetic sample,
which has bands attributed to Co 3+. The approximate path lengths of the
beam are 9 mm for the natural stone and 5 mm for the synthetic sample.
Unusual Be-Diffused Pink

Sapphire . . . A Cautionary Note
The Carlsbad laboratory recently
examined a 1.40 ct pink sapphire with
unusual orange color zones that was
submitted for a sapphire report. Initial
microscopic observation revealed
numerous thermally altered light-colored crystals, some of which were surrounded by discoid fingerprints (figFigure 25. The altered appearance of these crystals, which are
probably zircon, is consistent
with the high-temperature heat
treatment necessary for Be diffusion of the host sapphire.
Magnified 70.
ure 25), an inclusion scene consistent

with high-temperature heat treatment. Immersion revealed a planar
orange zone near the culet and a shallow orange zone parallel to the table
facet (figure 26). Orange color zones in
heat-treated pink sapphires may be
indicative of beryllium-diffusion treatment. However, when the stone was
tested by laserablation inductively
coupled plasmamass spectrometry
Figure 26. The orange color zones
along the culet and table of this
pink sapphire, as seen immersed
in methylene iodide, were caused
by Be-diffusion treatment. Magnified 10.
(LA-ICP-MS) in the girdle area (as is

GIAs standard practice, to avoid placing an ablation spot in an area that
could affect the stones appearance),
no Be was detected. This was not surprising because there was no orange
color near the girdle.
The orientation of the orange zoning in this sapphire was perpendicular
to the c-axis. This is a common orientation for natural orange zones in padparadscha sapphire that are caused by
trapped hole defects induced by an
excess of natural magnesium (J. L.
Emmett et al., Beryllium diffusion of
ruby and sapphire, Summer 2003
G&G, pp. 84135). To rule out such
orange zoning from naturally incorporated trapped hole centers, it was necessary to check for the presence of Be
directly in one of the orange color
zones. After obtaining permission
from the client, LA-ICP-MS measurements revealed more than 35 ppma Be
in an orange area, which is enough to
impart significant orange color in a
pink sapphire.
It was obvious from the shape and
orientation of the color zones that the
stone was beryllium-diffusion treated
as a tabular preform or piece of rough
that had sufficient sacrificial material
to allow all traces of Be to be removed
from the girdle area during cutting. It is
difficult to say whether this was a
deliberate attempt to defeat the standard practice of testing for beryllium in
the girdle. Nevertheless, careful gemological observation in immersion and
an understanding of color modification
in corundum prevented this Be-diffused sapphire from being misidentified as a standard heated sapphire.
Nathan Renfro and Amy Cooper
Unusually High Beryllium in

Three Blue Sapphires
Trace amounts of natural beryllium
are sometimes detected in untreated
sapphires, such as those from Madagascar. Typically, natural concentrations range from <1 ppma to about
45 ppma Be. Higher concentrations
(>15 ppma) are usually associated
with beryllium diffusion treatment.
232
LAB NOTES
GEMS & GEMOLOGY
FALL 2011
Nb AND Ta VS. Be
Nb or Ta (ppma)
50
40
30
20
10
Figure 27. This 3.21 ct sapphire

contained relatively high levels
of naturally occurring beryllium.
In addition, naturally occurring beryllium in corundum is often present
with traces (usually <1 ppma) of niobium, tantalum, light rare-earth elements, and thorium (see A. Shen et
al., From the GIA Laboratory: Beryllium in corundum: The consequences
for blue sapphire, GIA Insider, Vol.
9, No. 2, Jan. 26, 2007).
During routine testing, three blue
sapphires recently submitted for identification were found to contain relatively high levels of beryllium. The
three consisted of one ring-mounted
stone and two loose sapphires weighFigure 28. Higher concentrations
of Be in this blue sapphire (values in ppma are shown next to
each spot) were often associated
with the presence of milky
clouds. Magnified ~75.
LAB NOTES
0
0
10
15
20
25
30
35
Be (ppma)
Figure 29. The concentrations of niobium (Nb, circles) and tantalum (Ta,
triangles) showed an overall positive correlation to Be levels in the three
sapphires (red = 3.17 ct, blue = 3.21 ct, and green = mounted sapphire). To
convert to units of ppmw, the ppma values are multiplied by 0.44 for Be,
4.56 for Nb, and 8.87 for Ta.
ing 3.17 and 3.21 ct (e.g., figure 27).
Two of the samples showed microscopic evidence of heating, while the
other sapphire (3.17 ct) had inclusion
features that proved it was unheated.
The 3.21 ct stone showed a chalky
blue reaction to short-wave UV radiation (consistent with its low iron content) and strong blue bands when
viewed in immersion, while the other
two sapphires were inert to long- and
short-wave UV radiation due to their
relatively high iron contents. All
three stones contained milky clouds.
Trace-element analysis of all three
sapphires with LA-ICP-MS showed a
wide range of Be concentrations, from
virtually absent up to 33 ppma (figure
28). The concentrations of Be were, in
general, positively correlated to various
transition metals and light rare-earth
elements, including niobium, tantalum, tungsten, lanthanum, cerium,
hafnium, and thorium (e.g., figure 29).
Higher concentrations of all these elements, including Be, were often associated with the clouds, as documented
previously in Be-bearing untreated sapphires. Magnesium also showed a positive correlation with Be, but with large
variations. Titanium showed both positive and negative correlation with Be,
possibly due to Ti concentration variations in the blue zones.
The amount of Be in these sapphires is similar to or higher than that
recorded in some Be-diffused stones.
Their properties suggest that they
came from at least two different
deposits or deposit types, but their specific origins could not be determined.
This is another example showing that
thorough gemological and chemical
analysis is necessary to identify beryllium-diffusion treatment.
Ren Lu and Andy H. Shen
GEMS & GEMOLOGY
PHOTO CREDITS
Jian Xin (Jae) Liao1, 3, 5, 8, 12, 15, 16,
20 (left), 21, 23, and 27 (left); Kyaw Soe
Moe2, 17 (bottom), and 18; Wuyi
Wang4; Erica Emerson6 and 7;
Jason Darley10; David Nelson11;
Nathan Renfro13, 14, 25, and 26;
Sood Oil (Judy) Chia17 (top) and 23
(right); Nicholas Sturman20 (center);
Chunhui Zhou20 (right); JaeWon
Chang22; Ren Lu27 and 28.
FALL 2011
233
Editor
Brendan M. Laurs (blaurs@gia.edu)
Contributing Editors
Emmanuel Fritsch, CNRS, Team 6502, Institut des Matriaux Jean Rouxel (IMN), University of Nantes, France (fritsch@cnrs-imn.fr)
Michael S. Krzemnicki, SSEF Swiss Gemmological Institute, Basel, Switzerland (gemlab@ssef.ch)
Franck Notari, GGTL GemLabGemTechLab, Geneva, Switzerland (franck.notari@gemtechlab.ch)
Kenneth Scarratt, GIA, Bangkok, Thailand (ken.scarratt@gia.edu)
DIAMONDS
Type Ib greenish brown diamonds with a color shift.
Single substitutional nitrogen causes yellow color in diamond. Therefore, type Ib diamonds are often assumed to
be yellow (so-called canary diamonds). While this is true
for type Ib synthetic diamonds, only rarely do their natural
counterparts exhibit a pure yellow color. The most common color of type Ib diamonds is olive, a mixture of
green, brown-yellow, and gray. Some natural type Ib diamonds contain mixed orange and yellow colors, though
often with a brownish or greenish component. In our experience, pure brown samples are by far the rarest of the type
Ib diamonds, and they are seldom larger than 0.25 ct.
Recently, the GGTL laboratory received two greenish
brown diamonds (1.22 and 3.01 ct) for analysis that were
reportedly purchased directly from the mines in Simi, Sierra
Leone. FTIR spectroscopy showed they were pure type Ib,
with approximately 3.6 and 8 ppm, respectively, of single
substitutional nitrogen. In daylight-equivalent illumination,
the two diamonds were color graded Fancy Dark greenish
brown and Fancy yellowish greenish brown. However, they
showed a distinctly different coloration under incandescent
light, where they appeared Fancy Dark orangy brown and
Fancy orangy yellowish brown (figure 1).
When exposed to the 310410 nm broadband illumination of our fluorescence microscope, both diamonds exhibited very distinct, rather homogenously distributed reddish
orange luminescence. Exposure to standard UV radiation
gave similar fluorescence reactions: orange to long-wave
and a less intense orange to short-wave UV. Low-tempera-
ture (77 K) PL spectroscopy, using 405 and 532 nm excitation, identified the cause of the diamonds luminescence
as the NV0 center (575 nm), which dominated their spectra
(e.g., figure 2). In addition, the NV emission (637 nm) was
detected with 532 nm excitation (figure 2, bottom).
The diamonds UV-Vis-NIR spectra, obtained at 77 K
inside an integrating sphere under intense incandescent
illumination, showed the NV0 and NV emissions were
superimposed on the absorption continuum typical of
brown diamonds. Intense incandescent light efficiently
excited the NV0 and NV fluorescence, influencing the
apparent color of the diamonds.
It is important to note that the color grading of fancycolor diamonds actually includes the effect of fluorescence. For instance, purely yellow diamonds with strong
green luminescence can receive green color grades, even
though they do not have a greenish bodycolor. (However,
Figure 1. These 1.22 ct (top) and 3.01 ct (bottom)

greenish brown type Ib diamonds, seen under daylight-equivalent illumination (left), become distinctly orangy brown under incandescent light (right).
Photos by T. Hainschwang.
Editors note: Interested contributors should send information and illustrations to Brendan Laurs at blaurs@gia.edu or
GIA, The Robert Mouawad Campus, 5345 Armada Drive,
Carlsbad, CA 92008. Original photos will be returned after
consideration or publication.
234
GEM NEWS INTERNATIONAL
GEMS & GEMOLOGY
FALL 2011
PL SPECTRA
575
NV0
503
H3
INTENSITY
Raman
400
COLORED STONES AND

ORGANIC MATERIALS
460
520
580
640
700
760
680
740
800
860
575
NV0
637
NV
500
560
620
Gem-quality afghanite from Afghanistan. At the 2011

Tucson gem shows, Dudley Blauwet (Dudley Blauwet
Gems, Louisville, Colorado) exhibited several hundred
afghanites with a light blue color similar to that of aquamarine (e.g., figure 3). Mr. Blauwet purchased his first
rough piece of this material during a December 2009 trip
to Peshawar, Pakistan. His supplier was not certain of the
stones identity, only that it came from a group of mines
near the well-known Lajuar Madan lapis lazuli deposit in
the Sar-e-Sang district of Afghanistans Badakhshan
Province. The crystal yielded a clean 1.16 ct trilliant.
On a return visit in November 2010, Mr. Blauwet purchased two additional lots of the material, 96 g in all, from
a former partner of the original supplier. These were sold
to him as afghanite, an identity confirmed by electron
microprobe analysis (performed by Cannon Microprobe,
Seattle, Washington) of two crystals. They exhibited
hexagonal pyramidal terminations, which is typical of
afghanite. From this rough parcel, about 45 carats of clean
WAVELENGTH (nm)
Figure 2. The low-temperature photoluminescence

spectra of the 1.22 ct diamond at 405 nm (top) and
532 nm excitation (bottom) show that the orange
luminescence (inset, photographed under 310410
nm broadband excitation) is caused by the NV0
defect. Inset photo by T. Hainschwang.
near-colorless diamonds with extremely strong blue fluorescence are not color graded blue.) A notable example of a
diamond with this type of fluorescence-related color
change is the light brown Tavernier diamond, which
appears light pink in incandescent light (Y. Liu et al., The
alexandrite effect of the Tavernier diamond caused by fluorescence, Color Research and Application, Vol. 23, No. 5,
1998, pp. 323327, http://dx.doi.org/10.1002/(SICI)15206378(199810)23:5<323::AID-COL8>3.0.CO;2-Y). However,
the Tavernier is not considered a fancy-color diamond
since it belongs to the D-to-Z range.
We informed the client of the observed color shift
shown by the diamonds and noted the phenomenon on
their reports, with a comment stating that it was related to
fluorescence.
Thomas Hainschwang
(thomas.hainschwang@gemlab.net)
and Franck Notari
GGTL GemlabGemtechlab Laboratory
Balzers, Liechtenstein, and Geneva, Switzerland
Emmanuel Fritsch
Figure 3. These light blue afghanites (0.50, 1.16, and

0.23 ct) were faceted from material reportedly found
recently in Afghanistans Badakhshan Province.
Photo by Robert Weldon.
stones were cut, the two largest weighing 1.16 and 1.18 ct.
Later in November, Mr. Blauwet returned to Peshawar and
obtained another 320 g of rough sorted into four lots of various qualities. Some of these pieces also displayed the distinctive hexagonal pyramidal terminations. The two better
lots, which totaled about 65 g, featured clean facet-grade
material, including one piece that may eventually yield a
3.5 ct gem. Most of the lesser-quality rough was translucent, with some appearing silky.
Afghanite typically has a dark blue color, and gemquality stones are considered very rare (see Spring 2008
GNI, pp. 7980). Mr. Blauwet noted a strong demand for
this brightly colored afghanite in Tucson.
Stuart D. Overlin (soverlin@gia.edu)
GIA, Carlsbad
Iridescent ammonite from Madagascar. At the 2011 Tucson
Gem shows, Marco Campos Venuti (Seville, Spain) had iri-
GEMS & GEMOLOGY
FALL 2011
235
Figure 4. Ammonite from Madagascar showing

attractive iridescence is now being cut into cabochons, in addition to the polished fossils seen previously. The specimens shown here range from 2.8 to
6.4 cm long. Photo by Jeff Scovil.
descent fossil ammonites from southern Madagascar as
whole polished pieces as well as cabochons (figure 4).
Although this type of ammonite has been known for more
than a decade (see, e.g., Fall 2000 GNI, pp. 267268), this
was the first time that this author has seen it fashioned into
cabochons for jewelry use. Mr. Campos Venuti marketed
this material as Madammolite, and had about 50 cabochons that were cut into various shapes, as well as 100
matched pairs, ranging from 15 to 40 mm in longest dimension. He stated that the outer surface of the fossil must be
polished off to reveal the underlying iridescence; no stabilization or other treatments are performed on the material.
All of the pieces displayed red-orange iridescence, and small
areas of green and blue also were seen in a few cabochons.
The iridescent layer was very thin (<1 mm), and was better
developed on one side of the fossil than the other, which
created difficulty in cutting matched pairs. Fractures in the
material created an additional challenges for shaping the
cabochons. The iridescent patterns ranged from smooth and
homogenous to a pleasing ridged appearance.
The availability in a variety of shapes and matched
pairs gives designers interesting opportunities to incorporate these iridescent gems into jewelry, provided they are
properly protected from scratching or impacts that could
break the thin nacreous layer.
Brendan M. Laurs
stone) landscapes en route to the remote mountains that

host the aquamarine-bearing granitic pegmatites. From the
village of Xuan Le, motorbikes were used to traverse the
final 78 km to the base of the mountains, along a narrow
dirt track that crossed several streams on rickety 1-m-wide
wooden bridges.
A steep slippery footpath led from Lang Ben village up
to the mining area. After climbing slowly in the tropical
heat for about 1 hour and 40 minutesand passing an area
that reportedly was mined for topazthe trail emerged
from the jungle into an area containing dozens of shallow
pits mined for the aquamarine (e.g., figure 5). The workings
were sporadically distributed over a distance of ~400 m,
extending from an elevation of 592 m (1,943 ft) to 621 m
(2,039 ft). The pegmatites dipped almost vertically and
were highly decomposed. The shafts reached depths up to
15 m (figure 6), and horizontal tunnels were present at the
bottom of some shafts. There were no timbers or other supports, but the tunnels did not appear in danger of collapsing. No pumps or any other mechanized equipment were
present, probably due to the difficulty of the climb, and the
fact that hand tools were sufficient for digging through the
Figure 5. Aquamarine workings in Vietnams Thanh

Hoa Province consist of small pits surrounded by
dense jungle. Photo by D. Blauwet.
Aquamarine from Thanh Hoa Province, Vietnam: Mining

update. In May 2011, this contributor visited the aquamarine deposits on the west side of Thanh Hoa Province in
northern Vietnam (see L. T.-T. Huong et al., Aquamarine
from the Thuong Xuan District, Thanh Hoa Province,
Vietnam, Spring 2011 G&G, pp. 4248, http://dx.doi.org/
10.5741/GEMS.47.1.42). The journey started in Hanoi, the
home of Mr. Lai Duy, a close friend and guide for the trip.
We drove south on the main highway for about five hours
to Thanh Hoa city. Continuing on narrow side roads, we
passed lush rice fields and beautiful karst (weathered lime-
236
GEMS & GEMOLOGY
FALL 2011
Figure 6. At the Thanh Hoa

deposits, ropes are used to
hoist aquamarine-bearing
material from shafts (left).
Some of the shafts reach
depths of ~15 m (right).
Photos by D. Blauwet.
weathered deposit. According to a local miner, this area

had been worked for about four years, producing an estimated 5060 kg annually of mixed-grade aquamarine.
Climbing higher up the mountain to an elevation of
811 m (2,661 ft; coordinates 1950.7 N, 10509.7 E)
revealed an area that was actively being mined for aquamarine and topaz. These workings consisted of larger tunnels that penetrated deeper (1520 m) into the hillside but
at shallow angles. These pegmatites contained much more
quartz, with broken fragments up to ~20 cm seen in the
mine dumps. The quartz was generally opaque, white to
light smoky, and partially crystallized. Approximately a
dozen miners were active in this area, and they offered
small parcels consisting of broken fragments (13 g) and a
few complete crystals (up to ~7 cm long; figure 7) of attractive blue aquamarine. The crystals commonly had small
fractures along their length that would restrict the cutting
of clean stones to relatively small sizes but with good
color saturation (again, see figure 7). Colorless topaz was
occasionally found as small lustrous transparent crystals.
The miners indicated this area had been worked for several months.
This fascinatingand arduousexpedition provided a
first-hand view of these little-known aquamarine deposits,
which appear to have good potential for producing gemand specimen-quality material for many years to come.
Dudley Blauwet (mtnmin@q.com)
Dudley Blauwet Gems, Louisville, Colorado
Purplish blue and red-brown chalcedony from Peru. While
chalcedony often occurs in light blue hues, saturated blue
specimens are known from just a few localities, such as
Ysterputz in Namibia and Chikwawa in Malawi. Blue
chalcedony was found in Peru several years ago, but the
quality was not high and the material was only used locally. The exact locality is not publicly known, though initially it was believed to lie in the vicinity of Huachocolpa
in the Huancavelica region. This contributor was recently
informed by a reliable local dealer, who visited the locality, that the material comes from a site called Yanacodo,
about 30 km west of the city of Huancavelica. Recent production from this deposit (since 2010) is comparable to the
finest blue chalcedony from other sources (e.g., figure 8).
While in Lima in February 2011, this contributor saw several hundred kilograms of rough and at least 50 cabochons
measuring up to 4 cm across.
Ten pieces of rough and five cabochons were examined
by this contributor for this report. All were purplish blue,
and many displayed agate-like zoning. The samples had a
spot refractive index of 1.54 and a specific gravity of
2.602.61, consistent with published values for chalcedony, and no features were seen with the hand spectroscope. As expected, the material showed an aggregate reaction in the polariscope, which confirmed its fibrous structure. The chalcedony was inert to UV radiation, although
a few pieces contained veinlets that fluoresced white to
both long- and short-wave UV radiation.
Another unusual chalcedony from Peru appeared in
February 2011. It is reportedly from the vicinity of Santa
Ana village, about 30 km southeast of Huancavelica. The
chalcedony is red-brown and therefore can be described as
sard or carnelian. It contains small cavities that are usually
filled by colorless chalcedony. Although carnelian normally occurs as concretions in sedimentary rocks, here it
forms crusts and rarely even stalactites up to 3 cm long
(e.g., figure 9) within cavities hosted by volcanic rocks.
From a study of three pieces of rough and three table cuts,
its gemological properties were the same as for the blue
variety, except that it fluoresced green to long-wave UV
particularly in lighter colored areas.
Jaroslav Hyrsl (hyrsl@kuryr.cz)
Prague, Czech Republic
Figure 7. These Vietnamese aquamarines range from
1.5 to 7.1 cm long (crystals) and 1.34 to 6.96 ct (cut
stones). Photo by Robert Weldon.
GEMS & GEMOLOGY
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237
Figure 8. Fine blue chalcedony such as these pieces

(6.1 and 4.0 cm wide) became available from Peru in
2010. Gift of J. Hyrl, GIA Collection nos. 38420 and
38421; photo by Robert Weldon.
Update on emerald mining in Afghanistan. In May 2011,
author VP traveled to Afghanistan to collect reference samples for GIAs laboratory. Unfortunately, due to the security
situation in parts of Afghanistan, it was impossible to visit
the ruby mining area near Jegdalek or the various deposits
in Badakhshan. However, the authors spent three days in
the emerald mining area near the village of Khenj in the
Panjshir Valley (see, e.g., G. W. Bowersox et al., Emeralds
of the Panjshir Valley, Afghanistan, Spring 1991 G&G, pp.
2639, http://dx.doi.org/10.5741/GEMS.27.1.26).
We witnessed about 400 miners working in the Khenj
area. Mining is performed by groups of up to 20 people,
some working in day/night shifts. The most active site
was Kamar Safeed (figure 10), situated on cliffs at an elevation of 3,000 m. Up to 300 miners were working this site.
Figure 9. Carnelian from Santa Ana, Peru (here, 10.5
cm wide), rarely displays finger-like formations. Photo
by J. Hyrl.
Small groups were also active at Koskanda, Norola,

Siakolo, Habal, and Batak. The Michalak area, where several hundred miners were said to be active in 2010, was
practically abandoned. The Tartah and Dalnow deposits
have reportedly been exhausted. Security concerns prevented a visit to the emerald mining areas in the Panjshir
Valley located outside of the Khenj area (Dach Te Rivaat
and Mukeni), where operations are reportedly limited.
All of the mining activities witnessed at Khenj were
underground, in a maze of tunnels reaching 200 m deep.
Because conventional explosives cannot be legally
obtained in Afghanistan, miners were fabricating their
own by mixing fertilizer with the contents of old unexploded Soviet military ordnance (figure 11). These mixtures are too powerful for gem mining, and many fine
stones are consequently broken or fractured by the blasts.
Dealers in Kabul reported that emerald production had
been good during the past few months, and this was confirmed by miners in Khenj. The emerald parcels were said
to be exported to Pakistan or Dubai for faceting. The gems
were typically light green to deep green, often with very
good transparency. While most of the rough stones were
small (less than 1 g), we also saw several large fine emerald
crystals up to 6 g, as well as some attractive mineral specimens. A preliminary study of the emeralds obtained from
the Khenj area (e.g., figure 12) revealed that their inclusions mirror those normally seen in Colombian emeralds.
The situation at the emerald mines has improved since
VPs previous visit in 2006. Khenj can now be reached in
three hours from Kabul using a new road. Small hydroelectric power stations have brought electricity to the valley,
and the miners are using generators to light and ventilate
the tunnels. While working the Panjshir emerald mines
remains very difficult, the high-quality stones can provide
good income.
Figure 10. Situated on steep cliffs, Kamar Safeed is the

most active emerald mining area near Khenj, a village in
the Panjshir Valley of Afghanistan. Photo by V. Pardieu.
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and Industry. The whole process takes anywhere from

three days to a week. Streamlining the export process
would encourage legal exports, benefiting the local gem
industry and the country as a whole.
Vincent Pardieu (vpardieu@gia.edu)
GIA, Bangkok
Guy Clutterbuck
CGM Ltd., Dublin
A deep green fuchsite-rich rock. The Ricerche e Analisi
Gemmologiche (RAG) laboratory in Turin, Italy, received
for identification three samples of a deep green material
that resembled jadeite or nephrite (figure 13). No information was provided on the samples source. The material
consisted of thin slabs no more than a few millimeters
thick, with a fine granular structure characterized by a
deep green matrix and some very small white spots.
Figure 11. Afghan emerald miners mix fertilizer
with old Soviet military explosives for blasting purposes, which often damages the fragile crystals.
Photo by V. Pardieu.
The Afghan government faces many challenges, one of
which is replacing a complicated and inefficient rough
stone export system. According to one government official, the tax value of a parcel for export must be negotiated
and a 15% tariff paid, then another 9% is levied at the airport. In addition, several papers must be obtained from the
Ministry of Mines and the Afghan Chamber of Commerce
Figure 12. These emerald samples are from the Khenj
area of the Panjshir Valley. The cut stones weigh
~1.52 ct. Photo by V. Pardieu.
Figure 13. This polished slab (~32 mm long), resembling jadeite or nephrite, proved to be a rock composed
of fuchsite, albite, and sphene. Photo by R. Navone.
The samples RI, measured with a refractometer using
the distant observation technique, was between 1.53 and
1.56. The SG was 2.78 and the Mohs hardness was 55.
The material was inert to long- and short-wave UV radiation, and the handheld spectroscope showed general
absorption in the deep red region of the spectrum. The
samples had a fairly even color distribution and no apparent cleavage. At first glance, they could have been either
natural or artificial, as they resembled a compressed powder with some type of hardening media.
With the permission of the client, we cut a thin section
from one of the slabs for examination with a polarizing
microscope (figure 14). The matrix consisted of a colorless
to green foliated aggregate with low relief and low-order
interference colors, consistent with a mica-group mineral.
The thin section was also studied at the University of
Turins mineralogy department with a Cambridge S-360
scanning electron microscope equipped with an Oxford
INCA energy-dispersive spectrometer. SEM-EDS spectroscopy identified the material as fuchsite, the green
chromium-bearing variety of muscovite (in this case,
GEMS & GEMOLOGY
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239
Figure 14. Viewed in cross-polarized light, this thin section of one of the slabs shows bright interference colors
corresponding to Cr-bearing muscovite, gray low-relief
areas of albite (center), and high-relief grains with highorder interference colors that are sphene. Photomicrograph by E. Costa; image width ~0.5 mm.
1.01.5 wt.% Cr2O3). Also present was an anhedral gray to

white mineral with low relief; it was shown to be albite.
Finally, there were a number of high-relief inclusions, deep
yellow to brown and brownish black, with high-order interference colors; these were identified as sphene.
Figure 15 shows an SEM backscattered electron image of
the thin section, in which the gray tone is proportional to the
mean atomic number of the phase. The light grayappearing
matrix is the Cr-bearing muscovite, the dark gray areas are
albite, and the white portions represent sphene.
We detected no dyes, polymers, or other foreign media,
and the texture of the minerals demonstrated the materials
natural origin. We concluded that the slabs were cut and polished from a fine-grained metamorphic rock consisting predominantly of fuchsite. The material had an attractive green
color and could be used for cabochons or carving, although
with caution due to its relatively low hardness. Cabochons
consisting of fuchsite aggregates have been seen previously
(as emerald imitations; see Summer 2002 Gem News
International [GNI], pp. 183184), but those were more
translucent than the material documented here, and they
also contained inclusions of rutile and dolomite, rather than
the albite and sphene impurities in the present samples.
Emanuele Costa (emanuele.costa@unito.it)
Department of Mineralogy and Petrology
University of Turin, Italy
Raffaella Navone
RAG Gemological Laboratory, Turin
Figure 15. The texture of the green rock is well displayed in this backscattered electron image of the
thin section in figure 14, which shows Cr-bearing
muscovite (light gray), albite (dark gray), and sphene
(white). The black areas are microscopic pores in the
rock. Image by E. Costa.
Color-change garnet from Nandagala, Tanzania. Mark Saul

(Swala Gem Traders, Arusha, Tanzania) recently informed
GIAs Bangkok lab about a new deposit of color-change
garnet near Nandagala village, Lindi Province, southern
Tanzania. According to Mr. Saul, the stones were believed
to be alexandrite when first discovered in January 2011,
resulting in a minor gem rush and several dealers overpaying for rough. The garnet comes from two diggings: A primary deposit where small (typically <0.2 g) dark-colored
stones are found, and a nearby alluvial deposit that produces somewhat lighter pieces up to ~2 g. One large (>5 g)
clean stone from the alluvial deposit was faceted into the
11.81 ct gem in figure 16. The alluvial deposit also produces clean but nonphenomenal brownish orange garnets,
some of which exceed 20 g.
The five rough samples in figure 16 were purchased by
GIA, and four were polished with parallel windows and
examined for this report. Their color change was distinct,
showing greenish blue in fluorescent light and purplish red
or red in incandescent light. They had RI and SG values of
1.762 and 3.89, which are typical for color-change pyropespessartine (e.g., D. V. Manson and C. M. Stockton,
Pyrope-spessartine garnets with unusual color behavior,
Winter 1984 G&G, pp. 200207, http://dx.doi.org/10.5741/
GEMS.20.4.200). They were inert to long- and short-wave
UV radiation. With the desk-model spectroscope, the
Figure 16. Pyrope-spessartine from Nandagala,

Tanzania, shows a distinct
color change between daylight-equivalent fluorescent
(left) and incandescent (right)
light. The faceted stone
weighs 11.81 ct and the
rough pieces are 0.41.2 g.
Photos by V. Pardieu.
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GEMS & GEMOLOGY
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Figure 17. Partially healed fissures, needles, and black grains formed a typical inclusion scene in the colorchange garnet samples (left). Also present were zircon-like crystals (center; cross-polarized light) and another
type of dark reddish brown crystalline inclusion (right). Photomicrographs by V. Pardieu; magnified 40.
darkest sample showed a band at ~400 nm and a broad

absorption at ~570 nm; the latter feature was less obvious
for lighter stones with a weaker color change. The inclusion scene (figure 17) was dominated by needles, zirconlike crystals, partially healed fissures, and negative crystals. We also saw some black opaque, reddish brown, and
elongated greenish crystals. Unfortunately, the inclusions
were too deep in the samples to be identified with Raman
spectroscopy.
Chemical composition was measured using EDXRF
spectroscopy and a Thermo X Series II LA-ICP-MS.
The garnets had an average composition of Pyp51Sps40Grs3.5Alm3Gol2Uva0.5 (with 7300 ppm V and 1100 ppm
Cr). This was very similar to that reported for color-change
garnets from Bekily, Madagascar (K. Schmetzer and H. J.
Bernhardt, Garnets from Madagascar with a color change
of blue green to purple, Winter 1999 G&G, pp. 196201,
http://dx.doi.org/10.5741/GEMS.35.4.196).
UV-Vis absorption spectra were collected using a
PerkinElmer Lambda 950 spectrometer. A strong absorption band at ~570 nm (due to V3+ and Cr3+) dominated the
spectra of all samples (e.g., figure 18). This band created two
ABSORPTION COEFFICIENT (cm-1)
Figure 18. This UV-Vis spectrum of a light-colored

Nandagala garnet (3.3 mm thick) shows a broad absorption at ~570 nm due to V3+ and Cr3+, creating transmission windows in the blue-green and red regions.
UV-VIS ABSORPTION SPECTRUM

408
6
423
432
576
463
0
300
400
489
500
600
WAVELENGTH (nm)
700
800
transmission windows, in the blue-green (~480 nm) and red

(700 nm) regions, which are responsible for the color
change. The darkest sample showed a cutoff at ~440 nm,
while the lighter stones had a cutoff at ~310 nm and also
showed absorptions due to Mn2+ (408, 423, and 489 nm),
Fe3+ (432 nm), and Fe2+ (463 nm; see P. G. Manning, The
optical absorption spectra of the garnets almandine-pyrope,
pyrope and spessartine and some structural interpretations
of mineralogical significance, Canadian Mineralogist,
Vol. 9, 1967, pp. 237251).
This new Tanzanian deposit joins Kenya and Madagascar as another source of color-change garnet in the East
African region.
Vincent Pardieu, Kamolwan Thirangoon, and
Sudarat Saeseaw
GIA, Bangkok
An examination of some colorless gems from Myanmar.
This contributor recently had the opportunity to examine
rough and cut samples of four colorless gemsphenakite,
petalite, pollucite, and goshenite berylrecovered from
granitic pegmatites located near Molo village in Momeik
township, northern Shan State, Myanmar. At this locality,
pegmatite dikes intrude a peridotite body that is hosted by
gneiss, marble, and calc-silicate rocks of the Mogok Group.
The pegmatites primarily produce gem-quality pink tourmaline, along with other minerals such as topaz, beryl,
hambergite, quartz, and the colorless gems listed above
(see, e.g., figure 19 and U H. Kyi et al., The pegmatitic
gem deposits of Molo [Momeik] and Sakhan-gyi [Mogok],
Australian Gemmologist, Vol. 22, No. 7, 2005, pp.
303309).
The phenakite (Be2SiO4) crystals were distorted and
some were twinned. They showed etch marks on their
prism faces. The faceted gems usually weigh <1 ct.
Inclusions consisted of small growth tubes and tiny irregular solid crystals.
The petalite (LiAlSi4O10) crystals showed etched cleavages with deep channels. The material is transparent in a
range of sizes, yielding finished gems of 350 ct. Small
solid colorless rounded inclusions were present.
The rough pollucite (CsAlSi2O6. nH2O) did not show
any crystal faces, and its surfaces were cracked, pitted, and
GEMS & GEMOLOGY
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241
Figure 19. These samples of phenakite (2.5 ct), goshenite (4.9 ct), and pollucite (1.0 ct) are from the Momeik
area near Mogok, Myanmar. Photo by U T. Hlaing.
iron stained. Cut gems generally range from 3 to 6 ct.

Parallel lath-like solid inclusions and spiky crystals were
seen.
The goshenite crystals were tabular and typically yield
finished gems of 0.852.0 ct. The material was quite
included, with internal features consisting of two-phase
fingerprints, distorted needle-shaped crystals in random
orientations, and white opaque solids.
The gemological properties recorded from the
phenakite, petalite, pollucite, and goshenite samples were
within reported ranges. They can be differentiated from
one another by their standard gemological properties (e.g.,
RI and/or SG values) and sometimes by their morphologic
characteristics. The Burmese petalite is tabular to elongated with prominent cleavage, phenakite forms isolated prismatic crystals with rhombohedral terminations, goshenite
typically consists of short prismatic crystals, and pollucite
is recovered as broken pieces without any crystal faces.
U Tin Hlaing
Dept. of Geology (retired)
Panglong University, Myanmar
Nuummite from Mauritania. Iridescent orthoamphibole
(anthophyllite-gedrite) as a gem material was first reported
from Greenland nearly 25 years ago (P. W. Uitterdijk Appel
and A. Jensen, A new gem material from Greenland:
Iridescent orthoamphibole, Spring 1987 G&G, pp. 3642,
http://dx.doi.org/10.5741/GEMS.23.1.36). Until fairly
recently, this was the only known locality for this gem,
called Nuummite. The Greenland material is notable for
its golden iridescence, though blue iridescence has also
been seen (Spring 2000 GNI, pp. 7374).
In 2009, a new source of gem-quality iridescent
orthoamphibole was discovered in the Sahara Desert of
central Mauritania (see T. Kobayashi, Iridescent Nuumite, Gemmology, Vol. 41, No. 486, Issue 3, pp. 1415 [in
Japanese]). Three faceted stones and a piece of rough were
donated to GIA by G. Scott Davies (American-Thai
Trading, Bangkok). His company has cut more than 3,000
carats of this Nuummite, showing iridescence that is mostly bluish green, although some stones appear golden yellow
and a small percentage are a highly desirable pure blue (e.g.,
242
Figure 20. These samples of Nuummite (an aggregate

of iridescent orthoamphibole) from Mauritania weigh
9.2016.03 ct and illustrate the variation in color of
this material. Photo by, and gift of, G. Scott Davies;
GIA Collection nos. 3838438386.
figure 20). Finished stones are typically cut to between 10

and 20 mm, corresponding to a weight range of ~820 ct in
cabochon or faceted form. This size range is preferable
because the iridescence is not apparent in smaller stones,
and larger pieces can show an uneven color distribution.
Raman spectra of the iridescent laths were consistent
with anthophyllite and gedrite, which are orthorhombic
members in the magnesium-iron-manganese-lithium
amphibole group. The samples had RI measurements
between 1.649 and 1.669, consistent with the Raman identification. A second shadow edge also was noted at 1.54,
due to an additional mineral component in the rock.
Brassy metallic mineral grains, presumably pyrite, were
also seen in the samples. Hydrostatic SG was 2.98 0.05,
and all three stones were inert to long- and short-wave UV
radiation. With magnification, the iridescent phenomenon
closely resembled that of labradorite. It therefore seems
likely that the iridescence is caused by a lamellar structure
Figure 21. These Nuummite orthoamphibole laths show

blue iridescence on the outer perimeter that shifts to
greenish yellow toward the interior, suggesting a chemical variation within the crystal. Photomicrograph by
N. Renfro; magnified 20.
GEMS & GEMOLOGY
FALL 2011
Figure 22. Mechanized mining is once again producing

blue opal from Sinaloa,
Mexico (left). The opal is
hosted by rhyolite, and the
adjacent matrix is commonly silicified into perlite
(right). Courtesy of Blue
Opal Light Co.
of the orthoamphibole mineral grains. The iridescence displayed color zoning from blue to greenish yellow toward
the core of the crystals (figure 21). This type of concentric
zoning suggests a chemical variation in the amphibole.
This new find of iridescent orthoamphibole makes for
an interesting and unusual gem. This material has also
been offered by online dealers as spheres several centimeters in diameter.
Nathan Renfro (nrefro@gia.edu)
GIA, Carlsbad
Blue opal showing play-of-color from Sinaloa, Mexico.
Mexican opal is known mainly from Quertaro and Jalisco
States, which are most recognized for producing fire and
crystal varieties. Recently the owners of an opal mine in
Sinaloa State (Bertha Almaral, Marco Reyes, and Juan Vital)
showed this contributor a number of specimens that displayed a blue bodycolor and an attractive play-of-color.
The volcanic-hosted deposit is located near the town of
Cosal, approximately 137 km (85 miles) north of
Mazatlan. Although the site was discovered 25 years ago,
mining activity has been sporadic and limited to hand
methods. Under the ownership of Blue Opal Light Co.
since April 2011, operations have become mechanized. A
backhoe fitted with a hydraulic hammer is used to break
up the host rhyolite in search of opal concentrations (figure 22, left). This opal forms nodules and infillings in a
rhyolite lava flow, and is commonly surrounded by perlite
(figure 22, right). The owners estimate that only 10% of
the deposit has been mined.
Two cabochons (one loose and one mounted) were
briefly examined at GIA, and they had spot RI values of
1.46 and 1.47. The hydrostatic SG of the unmounted
sample was 2.32, but this value is not reliable due to the
presence of some matrix material in the cabochon. Both
samplesas well as several rough piecesshowed interesting UV fluorescence: They were inert to long-wave
but luminesced strong green to short-wave UV, with no
phosphorescence.
The opals (figure 23) are reportedly stable, as pieces discovered two decades ago have not shown any crazing. The
material will be marketed as Lightning Blue Opal, starting
in late 2011.
Stuart D. Overlin
pallasite from the Esquel meteorite. Pallasite is a rare type

of stony iron meteorite containing inclusions of transparent crystalline olivine (peridot) in an iron-nickel matrix
(for more information on pallasitic peridot, see the article
by A. Shen et al. on pp. 208213 of this issue). Faceted pallasitic peridot, though rare, has seen jewelry use in the
past. These pendants were unusual in that they combined
polished pieces of pallasite with mother-of-pearl to create
an attractive optical effect.
According to Mr. Falls, slices of pallasite were selected
based on the characteristics of the olivine crystals, which
need to be sufficiently large and transparent. These were
then polished and mounted on top of iridescent slabs of
mother-of-pearl, which were selected based on the pattern
and positioning of the iridescent areas. The sheen from the
mother-of-pearl helps to reflect light back through the
olivine crystals; the backs of the pendants also are left
open to allow light in from behind.
Mr. Falls reported that five of these pendants have been
produced to date, ranging from 2 to 5 cm long. They plan
to continue production as long as sufficient Esquel material is available.
Thomas W. Overton (toverton@gia.edu)
GIA, Carlsbad
Figure 23. These opals from Sinaloa represent higherquality material from the deposit. The loose cabochon weighs 30.41 ct, and the matrix specimen is
8.7 cm long. The earrings in the inset
contain opals measuring 21 12 mm.
Samples courtesy of Blue Opal Light
Co.; photos by Robert Weldon.
Pallasite pendants. Bob and Carol Falls of Rock Falls

Designs (Colorado Springs, Colorado) recently showed
GIA some interesting pendants (e.g., figure 24) set with
GEMS & GEMOLOGY
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243
Figure 24. This unusual pendant (2.5 3.0 cm) is

mounted with polished pallasite over mother-of-pearl.
Photo by Robert Weldon.
Figure 25. These Chinese freshwater cultured pearls

(1721 mm long) proved to be beaded by baroque
cultured pearls. Photo by E. Strack.
Chinese freshwater cultured pearls beaded with baroque

freshwater cultured pearls. This contributor recently examined a strand of Chinese freshwater cultured pearls loaned
by Jeremy Shepherd of Pearl Paradise, Los Angeles,
California. According to Mr. Shepherd, they were produced
at the same farm in Jiangsu Province that was the source of
the so-called Souffl pearls (beaded with mud) that
began appearing on the market in September 2009 (see
Spring 2010 GNI, pp. 6163).
The strand (figure 25) originally consisted of 23 cultured pearls weighing a total of 66.8 g; two were subsequently sacrificed for destructive testing (see below). They
were of baroque shape, ranging from 17.0 12.0 mm to
21.0 13.6 mm. Colors varied from white with a distinct
purplish green overtone to light purple, purplish green,
orange, and bronze with varying overtones. The five cultured pearls with a white bodycolor all showed strong blue
fluorescence to long-wave UV radiation; the others were
inert. All displayed a pronounced metallic luster (again,
see figure 25).
Thirteen of the 23 cultured pearls were examined by Xradiography. Strangely, all the X-radiographs showed beads
with an off-round shape (figure 26, left). In particular, the
internal features of the beads strongly suggested that nonbeaded freshwater cultured pearls had been used. To further investigate this possibility, one sample was sawn in
half (figure 26, center), revealing a concentric structure surrounded by an outer rim of nacre. The rim was clearly distinguishable from the inner portions and appeared more
yellowish with a uniform color distribution; its thickness
varied from 0.6 to 1.2 mm. A second sample was broken
apart with a jewelers hammer, confirming that a white
freshwater cultured pearl of baroque shape had been used
as a bead (figure 26, right).
According to Mr. Shepherd, these cultured pearls were
produced using the same type of mussel as the Souffls,
which some believe to be a hybrid of the Chinese
Hyriopsis cumingii and the Japanese Hyriopsis schlegelii,
though it may be a local variety of H. cumingii. This mussel shell shows a strange curvature on its outer rim that
Figure 26. The X-radiograph of the cultured pearls (left) revealed off-round beads displaying concentric growth
structures that were clearly visible when one sample was cut in half (center, 15.7 12.5 mm). When another
sample was broken apart (right, originally 17 12 mm), a baroque freshwater cultured pearl bead was exposed.
Photos by E. Strack.
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GEMS & GEMOLOGY
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Figure 27. The alleged hybrid of Hyriopsis cumingii and

Hyriopsis schlegelii used to produce these cultured
pearls shows an unexplained curvature at the rim (see
arrow) and intense iridescence. The shell (13 19 cm)
contains a blister pearl on the left (26.3 mm long), and
is shown with an assortment of mostly Souffl pearls
that are 1017 mm long. Photo by Jeremy Shepherd.
lacks explanation so far (figure 27). Similar curvatures have

been observed in old European pearl mussel shells
(Margaritifera margaritifera). It is also interesting to note
that the interior of the shell shows an array of intense
spectral colors. The cause of these metallic colors, which
are also visible in the resulting cultured pearls, has not yet
been determined. It is highly probable that both the
Souffl pearls and the pearl-beaded samples described
here are produced inside the mantle, probably in a later
growth phase, by making use of existing pearl sacks that
stemmed from a previous harvest.
Elisabeth Strack (info@strack-gih.de)
Gemmologisches Institut Hamburg, Germany
Quartz with spessartine inclusions. Brazils Navegadora
mine (Lavra da Navegadora) in the Conselheiro Pena area
of Minas Gerais State has been an important producer of
spessartine, mainly as etched crystals that are sought by
mineral collectors (e.g., J. S. White, Spessartine from the
Navegadora mine, Minas Gerais, Brazil, Rocks &

Minerals, Vol. 84, No. 1, 2009, pp. 4245, http://dx.doi.org/
10.3200/RMIN.84.1.42-45). The mine has also produced
attractive quartz with inclusions of spessartine, as displayed at the 2011 Tucson gem shows by Luciana Barbosa
(Gemological Center, Los Angeles). She indicated that the
material has been sporadically produced, but became significantly more available between 2009 and 2010. She
obtained enough rough material to cut and polish about
1520 pieces. This quartz has been worked into a wide
range of products (e.g., figure 28), ranging from 5 ct gems
to faceted stones in the 100 ct range and large polished
crystal points and spheres.
Although euhedral syngenetic spessartine has been
reported previously as inclusions in quartz (e.g., E. J.
Gbelin and J. I. Koivula, Photoatlas of Inclusions in
Gemstones, ABC Edition, Zurich, Switzerland, 1986, p.
159), the availability of this material in significant quantities and sizes is notable.
Brendan M. Laurs
Pink cats-eye quartz, with color and chatoyancy caused by
tourmaline needles. Chatoyant quartz is widely available
in gray, yellow, and green, and it is often misrepresented as
chatoyant chrysoberyl. Recently, this contributor examined a pink cats-eye quartz that proved interesting because
of the unusual cause of the color and chatoyancy.
The 34.65 ct specimen (figure 29) displayed a broad but
distinct chatoyant band with a dull vitreous luster. At first
glance, it was reminiscent of chatoyant tourmaline
because of its color. Closer examination with the unaided
eye showed color concentrations in various areas, especially toward the sides. This suggested the presence of a dye
along the growth tubes/surface breaks. The specimen
appeared anisotropic under crossed polarizers, with some
interference colors perpendicular to the chatoyant band or
along the direction of the needles. This suggested a uniaxial mineral, although a clear optic figure could not be
resolved due to the dense inclusions. Spot RI and hydro-
Figure 28. These quartz

specimens from Brazil contain well-formed inclusions
of spessartine. The faceted
stone weighs 18.60 ct (photo
by Robert Weldon) and the
cabochon weighs 25.60 ct
(photo by Luciana Barbosa).
GEMS & GEMOLOGY
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245
Figure 29. This 34.65 ct quartz specimen, despite its

resemblance to rose quartz, owes its pink color and
distinct chatoyant band to the presence of tourmaline needles. Photo by G. Choudhary.
static SG were measured at approximately 1.54 and 2.68,

respectively. The sample displayed no reaction to UV radiation, and no features were seen with the desk-model
spectroscope. These properties indicated quartz, but further analysis was required.
With magnification, the sample displayed long tube or
needle-like inclusions (figure 30). From the side, some
pink color was observed along these tubes, which again
raised suspicion regarding the cause of color. The crosssection of the tubes was even darker. At higher magnification, some appeared perfectly triangular (figure 31), a feature typically associated with trigonal minerals such as
tourmaline. This was further supported by the color of the
tubes and the absorption along the c-axis: The inclusions
appeared darker when viewed in cross-section. Hence, the
bodycolor of the sample was colorless but appeared pink
due to the colored inclusions.
IR transmission spectra were obtained both parallel
and perpendicular to the needles. In the parallel direction,
Figure 30. Viewed with magnification, the needles
appeared pink while the rest of the sample was colorless. This suggested that the quartzs pink appearance was due to these inclusions. Photomicrograph
by G. Choudhary; magnified 48.
Figure 31. The cross-section of the needles in figure

30 displayed a perfect triangular shape typically
associated with minerals belonging to the trigonal
system, such as tourmaline. Photomicrograph by
G. Choudhary; magnified 64.
two sets of distinct peaks were seen: in the 48004200
cm1 region (4594, 4534, 4438, and 4343 cm1) and in the
37003000 cm1 region (3585, 3563, 3480, 3379, 3300, and
3197 cm1). According to our database and past studies (see,
e.g., L. T. M. Oanh et al., Classification of natural tourmalines using near-infrared absorption spectroscopy, VNU
Journal of Science: Mathematics Physics, Vol. 26, 2010, pp.
207212; G. Choudhary and S. Fernandes, Spectroscopic
examination of commercially available quartz varieties: A
gemological perspective, Summer 2011 G&G, pp.
146147), the first set of peaks is similar to those seen in
tourmaline, while the second corresponds to those seen in
quartz. In the perpendicular direction, only a broad absorption band was observed in the 37003000 cm1 region, due to
the lower degree of transmission in that orientation.
On the basis of microscopic examination and the infrared
spectra, we identified this sample as quartz with inclusions
of pink tourmaline. Tourmaline is a common mineral inclusion in quartz, but typically it is randomly oriented. Thus,
this sample was interesting and unusual because of its pink
color (though it was not rose quartz) and chatoyancy. Both
were caused by the presence of parallel tourmaline needles.
Gagan Choudhary (gtl@gjepcindia.com)
Gem Testing Laboratory, Jaipur, India
An exceptional rhodochrosite carving. Rhodochrosite, a
manganese carbonate mineral known for its classic rosered color, is often found as massive pink opaque or translucent specimens. Such material is available in large sizes
and typically fashioned into ornamental carvings, beads,
and cabochons. Transparent specimens, however, are relatively rare.
The Gem Testing Laboratory of Jaipur, India, recently
tested a carved specimen (figure 32, left) that was remarkable
for its size and fair degree of transparency. The color was
uneven, ranging from brownish red to reddish brown to
brownish pink. The specimen weighed 10.875 kg and measured approximately 21.60 20.50 15.60 cm. It was carved
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GEMS & GEMOLOGY
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Figure 32. This carved

rhodochrosite is exceptional for its size (10.875
kg), rich brownish red
color, transparency, and
artistic quality. Photos by
M. B. Vyas.
in the form of Lord Mahaveera, one of the ancient Indian

sages who established the tenets of Jain Dharma. The piece
was also noteworthy for the fine artistic work on the back,
which is unusual (figure 32, right).
Although the bodycolor clearly suggested rhodochrosite,
we conducted gemological tests to establish the identity.
However, the carvings large size impeded our ability to measure all the properties. Its relatively dull luster indicated a low
hardness, which was confirmed by scratching an inconspicuous spot on the base with fluorite. The spot RI of around 1.60
displayed a large birefringence blink, typically associated with
carbonate minerals. A weak red reaction was visible with
long- and short-wave UV radiation, and the handheld spectroscope showed strong absorption bands centered at ~460 and
550 nm. We could not measure the carvings specific gravity,
but its heft indicated a somewhat high SG value.
Examination with strong fiber-optic light and a loupe in relatively transparent areas revealed three directions of cleavage (figure 33), a feature associated with calcite-group minerals such as rhodochrosite. In addition, some portions on
the back had rhodochrosites characteristic irregular to
wavy concentric banding patterns (figure 34).
Identifying this specimen was not particularly difficult,
even though its size did not allow the measurement of all
gemological properties. Encountering such a large and

finely carved rhodochrosite with attractive color and transparency was truly a pleasure.
Gagan Choudhary and Meenu Brijesh Vyas
Gem Testing Laboratory, Jaipur, India
Figure 33. Relatively transparent areas of the carving displayed the three directions of cleavage that are associated
with the calcite group of minerals. Photo by M. B. Vyas.
Figure 34. Areas of the carving showed rhodochrosites characteristic wavy to irregular growth
banding. Photo by G. Choudhary.
Sapphire and zircon from Ethiopia. In March 2010, Farooq

Hashmi (Intimate Gems, Glen Cove, New York) loaned
GIA several rough and faceted sapphires that he obtained
on a buying trip to Ethiopia. According to Mr. Hashmi, the
stones came from Yabelo in southern Ethiopia, 185 km
northwest of the Moyale border with Kenya. The sapphires (figure 35) are associated with reddish brown zircon
(figure 36) in secondary deposits. He reported that the
rough zircon was generally available in the 0.53 g range,
and that production of better-quality sapphire and zircon
typically has been about 1 kg per month.
The sapphires ranged from yellow to brownish green to
blue, and many of the rough pieces showed strong yellow and
blue color zones. The four faceted sapphires examined
(0.341.32 ct) were cut as round brilliants with the optic axis
oriented approximately perpendicular to the table. They yielded the following properties: RIno = 1.765, ne = 1.775; birefringence0.010; SG3.954.03, with the more reliable values
GEMS & GEMOLOGY
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Figure 35. These sapphires are from a new deposit in

Ethiopia. The four faceted samples (cut by Matt Dunkle,
Aztec, New Mexico) range from 0.34 to 1.32 ct; the largest
rough stone is 12.06 ct. Photo by Robert Weldon.
of 3.99 and 4.00 coming from the larger specimens; UV fluorescenceinert to both long- and short-wave UV radiation,
except for one yellow stone that fluoresced very weak orange
to long-wave UV; and bands at 450, 460, and 470 nm seen
with the desk-model spectroscope. Microscopic examination
(figure 37) revealed sparse long needles, dense clouds of short
needles and particles, equatorial thin films, and reddish brown
platelets of hematite (identified by Raman spectroscopy). Unidirectional twinning was also seen in one rough specimen.
UV-Vis-NIR spectroscopy of the sapphires confirmed
the Fe3+ absorption features at 450 (very strong), 460, and
470 nm, as well as strong peaks at 376 and 386 nm
attributed to Fe2+-Ti4+ intervalence charge transfer. In addition, the blue to green stones exhibited a broad intervalence charge transfer absorption due to iron in the
800900 nm range.
The trace-element composition of three representative
sapphires measured by EDXRF spectroscopy showed relatively high levels of Fe in all colors, small amounts of Ga
and Ti, no detectable V, and no Cr except in the yellow
stone (table 1). These properties are consistent with sapphires of magmatic origin.
A 13.01 ct zircon (again, see figure 36) was also exam-
Figure 37. The faceted dark blue-green sapphire in

figure 35 contained needles (probably rutile), clouds,
and equatorial thin films. Photomicrograph by D.
Beaton; image width 1.0 mm.
ined for this report. Its RI was >1.81, SG was 4.70, and it
fluoresced weak orange with yellow chalkiness to shortwave UV radiation. Magnification revealed strong doubling and wispy stringers of reflective particles. Its properties are consistent with high-type (non-metamict)
unheated zircon.
Donna Beaton (donna.beaton@gia.edu)
GIA, New York
TABLE 1. Chemical composition of sapphires from

Yabelo, Ethiopia.
Oxide (wt.%)
TiO2
Cr2O3
Fe2O3
Ga2O3
a
Figure 36. Reddish brown zircon is mined with sapphire in the Ethiopian deposit. This unheated 13.01
ct oval brilliant was cut by Hassan Z. Hamza (Noble
Gems Enterprises, Dar es Salaam, Tanzania) from
the largest piece of rough seen by Mr. Hashmi. Photo
by Robert Weldon.
248
Olive green
Yellow
Dark blue-green
0.009
nda
1.438
0.011
0.002
0.001
1.037
0.010
0.004
nd
0.928
0.010
nd = not detected.
Update on sapphire mining in Sri Lanka. In MarchApril

2011, this contributor visited several sapphire deposits in
Sri Lanka to gather information and collect samples for
the GIA laboratory reference collection. The trip assistants
included recent graduates from GIAs Bangkok campus
(Andrea Heather Go of Canada and Afsaneh Tazari of
Iran), David Goubert of Switzerland, and Jeremy Brian and
Jonathan Muyal of France. Our work was facilitated by
ICA members Armil Samoon (Sapphire Cutters Ltd.,
Colombo) and Gamini Zoysa (Institute of Gemmological
Sciences, Colombo).
The region around Ratnapura continues to be the most
active gem mining area. We saw 14 mechanized operations in the area (e.g., figure 38), quite an increase compared to the authors previous visit in 2005 when only one
such mine was working. Most of the operations use water
GEMS & GEMOLOGY
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Figure 38. Several mechanized mines are active in Sri

Lanka, including this operation at Kuruwita near
Ratnapura. Photo by V. Pardieu.
cannons and gravel pumps inside the pits, and some use an
excavator to bring the gem-bearing gravels (illam) to trommels and jigs for processing. We also witnessed traditional
pit mining in paddy fields and rivers, and well as hillside
mining that takes place where the gem-bearing layers are
very close to the surface (figure 39). The area produces
mainly blue (typically with some yellowish zones), yellow,
pink, and geuda sapphires (e.g., figure 40). Gem mining and
trading around Ratnapura is well regulated. Most operations possess mining licenses, and the production is usually sold through an auction system. The region hosts several busy gem markets, as well as cutting and treating centers. A number of treaters are active using both modern
and traditional heating methods.
The second most active mining area is near Elahera
(especially the Matale District). We visited nine mechanized operations scattered over a large area. Activities
were somewhat limited due to early rains, and we were
informed that 2030 excavators are expected to be working in the area after seasonal agricultural activities are
completed. In addition, several hundred small-scale traditional mines are anticipated. Unfortunately, a dam project
near Elahera is expected to flood some potentially rich sapphire prospects, raising concerns among miners. This
region is drier than Ratnapura and the gem gravels are not
as deep. The miners usually dig during the dry season,
stockpile the gem gravel, and then wash it during the rainy
season. Production includes sapphire, ruby, garnet, tourmaline, zircon, chrysoberyl, and many other gems. The
sapphires are mainly blue, geuda, and yellow; pink is least
common. The blue sapphires can be extremely fine and
are usually more evenly colored than those found around
Ratnapura. The rubies (very rare) are usually pinkish with
some blue zoning.
Our next stop was Hasalaka to the south in the highlands. There was little activity, reportedly due to the rice
harvest; up to 3,000 people were said to be active there
recently. We saw sapphires that were yellow, ottu type
(blue on the surface with a colorless or yellowish core), and
geuda; most had very good crystal shape.
Figure 39. Artisanal hillside mining in Sri Lanka

involves digging shallow pits to reach gem-bearing horizons, as shown here near Balangoda, about 35 km east
of Ratnapura. Photo by V. Pardieu.
Further southeast, we visited a large mechanized mine
near Bibile where several excavators were being used to
recover mainly geuda and yellow sapphires. The operation
reportedly started about one year ago and was similar to
the other large pits we saw near Ratnapura.
Continuing south, we documented some mechanized
operations in paddy fields to the north of Passara. The production consisted mainly of yellow, geuda, pink, padparadscha, and some blue sapphires; most of the crystals were
well formed. Further south toward the coast we visited
Okkampitiya and Kataragama. Although we saw some
evidence of mining in these areas, there was little activity
due to heavy rains.
Vincent Pardieu
Green cats-eye spodumene from Brazil. At the 2011
Tucson gem shows, Luciana Barbosa showed this contributor some green spodumene that displayed chatoyancy
(e.g., figure 41). The material was reportedly mined from
Figure 40. These sapphires were seen near Niwitigala
in the Ratnapura area. Photo by V. Pardieu.
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249
Figure 41. This green spodumene from Brazil (4.35 and

6.15 ct) shows chatoyancy. Photo by Robert Weldon.
the Neves pegmatite in the Araua area of Minas Gerais

State. Although the deposit has been a source of facetgrade green spodumene for years, Ms. Barbosa first saw
small parcels of the chatoyant material in 2010; only
about 5% of the production shows this effect, yielding
enough rough material to polish about 25 cabochons.
While clean faceted stones may reach 20+ ct, the cats-eyes
tend to be smaller, typically as cabochons weighing 58 ct.
The material is reportedly not treated in any way.
Although GIA has seen several examples of cats-eye
kunzite, green spodumene showing chatoyancy is much
more unusual (S. F. McClure, pers. comm., 2011).
Chatoyant kunzite has been reported previously (Kunzitkatzenaugen aus Brasilien [Kunzite cats-eye from Brazil],
Gemmologie: Zeitschrift der Deutschen Gemmologischen
Gesellschaft, Vol. 46, No. 2, 1997, pp. 6465, and references therein), but this is the first time that green material
has been documented in the literature, to this authors
knowledge.
Brendan M. Laurs
A color-zoned topaz. The Gem Testing Laboratory in
Jaipur, India, received for identification a transparent yellowish to greenish brown specimen that was striking for
its unusual color zoning. The oval mixed cut (figure 42)
weighed 27.38 ct and measured 21.18 16.39 9.64 mm.
The specimen initially appeared to be a sapphire because
Figure 42. This 27.38 ct topaz shows unusual color zoning, with a pattern resembling that seen in sapphire.
Photo by G. Choudhary.
of the pattern of its color zoning, but the luster and brilliance were lower than would be expected.
The stone had refractive indices of 1.6211.629, with a
birefringence of 0.008 and a biaxial positive optic sign. The
hydrostatic SG was 3.57, and moderate greenish brown to
brown pleochroism was observed. The sample was inert to
long-wave ultraviolet radiation and displayed a weak green
reaction to short-wave UV. No absorption features were
observed with the desk-model spectroscope. The RI and
SG values were consistent with topaz; the RIs indicated an
intermediate OH/F composition, while the SG was consistent with F-rich topaz (R. Webster, Gems, 5th ed., rev. by
P. G. Read, Butterworth-Heinemann, Oxford, UK, 1994,
pp. 150163).
When the topaz was immersed in bromoform, the
color zones became sharper and more prominent (figure
43), and they were still reminiscent of those seen in sapphire. The angles formed by the zones varied with viewing
direction. Viewed from the table, the angles were approximately 40/140 (figure 43, left); from the side, they were
70/110 (figure 43, right). These angles are different from
those seen in corundum (60/120). We were unable to find
any reference in the literature to such angles formed by
the crystal faces of topaz; the pyramidal faces {111} and
{111} only form an angle of 39 (E. S. Dana, Mineralogy,

4th ed., rev. by W. E. Ford, Wiley Eastern Ltd., New Delhi,
1949, pp. 613615). The intersection of the color zones did
Figure 43. The angles formed

by the color zones in the
topaz were different when
viewed from the table (left)
and the side (right). Also
note the planes of intersection, which form a zigzag
pattern. Photos by G.
Choudhary.
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Figure 44. The topaz contained tiny transparent crystal

inclusions associated with streams of fine pinpoints,
forming comet-tail patterns. Photomicrograph by
G. Choudhary; magnified 45.
at least 100 kg of rough, although much more material has

probably been produced since then.
Ten rough pieces and six cabochons (up to 4 cm across)
were examined for this report. All were identified as
variscite by X-ray diffraction, regardless of their color. The
cabochons yielded the following gemological properties:
spot RI1.551.56; SG2.122.23 (lower for material
with cavities); Mohs hardness34; streakcolorless;
UV fluorescenceweak green-yellow reaction to longwave and inert to short-wave UV; and no features seen
with the hand spectroscope. While these samples were not
treated, polymers can enhance variscites durability and
utility for jewelry.
Jaroslav Hyrl
SYNTHETICS AND SIMULANTS

not form a smooth plane but rather a zigzag pattern (again,
see figure 43, left). Therefore, the exact orientation of these
color zones is unknown and can only be assumed to be
aligned with the pyramidal faces.
With magnification, the sample was mostly clean,
except for a few tiny transparent crystals associated with
streams of fine pinpoints that formed comet-like patterns
(figure 44). Similar inclusions were documented in topaz
by E. J. Gbelin and J. I. Koivula (Photoatlas of Inclusions
in Gemstones, Vol. 2, Opinio Publishers, Basel,
Switzerland, 2005, pp. 751752).
This is the first time this contributor has encountered
topaz with a distinct color zoning pattern.
Gagan Choudhary
Variscite from Peru. Green variscite is a popular ornamental material that is best known for the attractive nodules
from Clay Canyon, Utah (W. E. Wilson, Famous mineral
localities: The Clay Canyon variscite mine, Fairfield,
Utah, Mineralogical Record, Vol. 41, No. 4, 2010, pp.
321349). More recently, gem-quality variscite was found
in the Meekatharra District in Western Australia (Spring
2007 GNI, pp. 6364).
In 2009, a new find of variscite was discovered in Peru.
The material was initially thought to be green turquoise,
and its locality was kept secret. An abundance of rough
came to market in early 2011, reportedly from the vicinity
of Yauli, 20 km east of the city of Huancavelica and ~200
km southeast of Lima. The geological position of the find
is not known, but variscite normally originates near the
earths surface from the interaction of Al-rich rocks with
meteoric phosphate-bearing waters. The Peruvian rough
forms veins rather than nodules, and is usually light green
or rarely gray-green (figure 45). It typically contains hollow
cavities, which can be up to 2 cm long; these diminish a
specimens value. Nevertheless, cabochons can be quite
attractive. Some of the gray-green material shows a lamellar agate-like structure (see the stone on the right in figure
45). While in Lima in February 2011, this contributor saw
An accidental corundum and lead glass triplet? In

December 2010, one of these contributors (P-YC) acquired
a parcel of six oval black cabochonssold as star sapphiresthrough several dealers from Chanthaburi,
Thailand via eBay. Since the Gemmological Association of
All Japan (GAAJ) laboratory had described black star sapphires treated with lead glass (Lead glass filled black star
sapphire, Gemmology, Vol. 39, No. 470, issue 11, 2008, p.
2), the parcel was inspected carefully, and one cabochon
exhibited an unusual feature. At 10 magnification, the
6.01 ct stone appeared to have a thin transparent section
through the center, roughly parallel to its base and ~0.5
mm thick at its widest point (figure 46). Standard gemological testing gave the expected spot RI of ~1.76 and a
hydrostatic specific gravity of 4.00. Some fractures contained a foreign material with an RI close to that of corundum, as evidenced by their similar luster in reflected light.
The unusual transparent layer appeared yellow and con-
Figure 45. These variscites are from a new find in Peru.

The pear-shape cabochon is 14.76 ct and the oval is 9.81
ct. Gift of J. Hyrl, GIA Collection nos. 38422 and
38423; photo by Robert Weldon.
GEMS & GEMOLOGY
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251
Figure 46. This corundum and

lead glass triplet (6.01 ct) shows a
thin transparent yellow layer with
included gas bubbles when
viewed from the side in benzyl
benzoate immersion. The cabochons general appearance is
typical of black star sapphires from Thailand (inset). Photos
by E. Fritsch and B. Rondeau (inset).
tained numerous gas bubbles, suggesting a glass. Some of

the bubbles reached the surface, creating cavities.
The stone was examined with a JEOL 5800 scanning
electron microscope. The transparent section showed a
Figure 47. In this backscattered electron micrograph, the

transparent layer in the black star sapphire shows a light
tone indicative of a high atomic number, consistent
with a high lead content. A surface-reaching bubble is
seen in the center; note that the two sides of the fracture
do not correspond in shape. Image by E. Fritsch.
contrasting tone, even in secondary electron imagery. The

contrast was even more pronounced in a backscattered
electron image (figure 47), which is sensitive to atomic
number. Chemical analysis with a PGT IMIX secondary
X-ray detector indicated that the transparent layer was
composed of Pb, Si, Al, and O, strongly suggesting a leadbased glass. The matrix was clearly corundumcontaining only aluminum and oxygenbut elsewhere in the
stone the lead-based substance could be found in narrow
fractures, mostly parallel to the base.
Because the top and bottom edges of the transparent
layer did not correspond in shape (again see figure 47), it
was not a fracture filling in a single crystal. The relative
crystallographic orientation of the two halves, examined
using strong lateral fiber-optic illumination to reveal
growth zones, also differed. The upper half showed a typical dark brown chevron, with one side roughly parallel to
the long axis of the stone, while the bottom half had
stripes that were nearly parallel to the short axis. This
meant that both sections shared roughly the same optic
axis plane, but were rotated ~30 from one another.
The two halves of this cabochon were likely treated
with lead glass as part of a larger parcel of black star sapphire rough. By chance, two crystals showed parting perpendicular to the c-axis, and those two parting surfaces,
both approximately flat, came in contact during the treatment. When the molten lead glass solidified, the two
halves were fused together and cut into a cabochon, leaving a thin layer of lead glass between them. This cabochon, then, would be most properly described as a corundum-glass-corundum triplet.
Emmanuel Fritsch
Pierre-Yves Chatagnier
Centre de Recherches Gemmologiques, Nantes, France
Benjamin Rondeau
CNRS, Team 6112, Laboratoire de Plantologie
et Godynamique, University of Nantes, France
Stefanos Karampelas
Gbelin Gem Lab, Lucerne, Switzerland
Elose Gaillou
Carnegie Institution, Washington, DC
Glass triplet resembling coated mystic topaz. Recently
these contributors received from India a 10.32 ct oval
mixed cut that had been purchased as a coated mystic
topaz. However, when viewed from the side, the samples true nature as a triplet became apparent (figure 48).
A thin iridescent layer ran through its center, between
colorless top and bottom halves, and the mystic effect
was reflected throughout the specimen. When placed in
an immersion cell with water, the triplet lost most of its
colorful appearance.
Both the top and bottom were singly refractive with an
RI of 1.581, and the hydrostatic SG was ~2.47. In the polariscope, it displayed anomalous double refraction when
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GEMS & GEMOLOGY
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layer inside a triplet creates a much more durable multicolor effect. However, since the coating is parallel to the table,
it reflects and colors any surface scratches and breaks (figure 49), thus making these defects far more visible than on
externally coated stones. Although such a triplet is not particularly difficult to design and produce, this is the first
example we have seen.
Olivier Segura (o.segura@bjop.fr)
Laboratoire Franais de Gemmologie, Paris, France
Emmanuel Fritsch
Figure 48. The two halves of this colorful glass triplet

(12.28 17.33 7.92 mm) are easily visible to the
naked eye. The junction between them is seen within
the frosted girdle. Photo by O. Segura.
viewed from the side. We saw no internal characteristics

with magnification, only some rounded facet junctions.
All of these features are consistent with glass.
Energy-dispersive chemical analysis using an EDAX
instrument revealed Si and K as major components, with
impurities of Ti, Fe, Zn, and Zr. This composition is typical of glass, and has been seen previously in other glass
imitations, although the Ti might be attributed to the
layer creating the iridescent effect.
Mystic topaz was first introduced in 1998 by Azotic
Coating Technology (Rochester, Minnesota) as an enhancement of colorless topaz with a thin-film coating of undisclosed material. Today, many firms worldwide use the
same process with topaz, quartz, and glass. Although the
coating is quite resistant, it can be scratched or damaged by
abrasives, chemicals, or an ultrasonic cleaner. Thus, coated
gems cannot be recut or repolished. Placing the iridescent
Figure 49. Viewed face up, the internal iridescent

layer in the glass triplet reflects scratches on the
table. Photo by O. Segura.
CONFERENCE REPORTS
ICA Congress 2011. Fair trade certification is not yet available for gemstones, but it is clear that the movement is
gaining grassroots support. Fair trade, corporate social
responsibility, and supply chain issues were central topics
at the 14th biennial International Colored Gemstone
Association (ICA) Congress in Rio de Janeiro, May 14. In
the more than 20 presentations delivered at the conference, industry leaders urged ICAs international delegates,
which include miners, gem wholesalers, and gemstone
dealers, not to ignore these issues in the colored stone
industry. Highlights of some of the presentations are given
below.
Eli Izhakoff of the World Diamond Council, New
York, a key player in developing the Kimberly Process
certification scheme for diamonds, urged delegates to recognize problems and develop defensive strategies, much
like the WDC does to stay ahead of issues with conflict
diamonds. Andy Lucas of GIA in Carlsbad used video
examples of how rural communities develop skills
through education and training, which he said leads to
social sustainability and poverty alleviation in mining
areas. He highlighted GIAs efforts at developing educational programs to meet those needs. Vincent Pardieu of
GIA in Bangkok suggested that remote gem locales develop partnerships with existing civic groups, such as those
protecting game reserves and national parks, to advance
social and environmental responsibility. This contributor
noted that in the absence of a fair trade label for gemstones, there are many things that small- and mediumscale miners can do to alleviate poverty, protect the environment, and ensure the supply chain from mine to market. Some miners and gem dealers are already creating a
blueprint for doing the right thing in the gem business,
such as Eric Braunwart of Columbia Gem House, who
asks his suppliers, employees, and other stakeholders to
sign and uphold a series of Quality Assurance and Fair
Trade Gems Protocols.
Congress attendees also heard from other segments of
the industry, including policy makers and gem miners. Dr.
Gaetano Cavalieri of the World Jewellery Confederation
(CIBJO), Milan, Italy, discussed the CIBJO Blue Books,
which promote standards for nomenclature and disclosure
codes for gem treatments. He described CIBJOs commit-
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253
ment to social and economic responsibility through the

development of the World Jewelry Confederation
Education Foundation under the auspices of the United
Nations Millennium Development Goals. Ian Harebottle,
CEO of Gemfields, London, which mines for emerald in
Zambia, noted that his company focuses on social sustainability by supporting local schools, medical clinics, and
farming projects, as well as working in partnership with
other stakeholders. Gemfields sells off old equipment
rather than discarding it, plants trees in waste dumps, and
fills nonworking pits with water and stocks them with
fish. He pointed out that such efforts also need to be economically sustainable: They are only made possible by
mining consistent supplies of rough gems, investing in key
resources, and developing marketing campaigns to ensure
stable market prices.
Representatives from two laboratories pointed to their
efforts in determining gemstone country of origin, which goes
to the heart of supply chain issues, particularly in areas of
conflict. Dr. Dietmar Schwarz of the Gbelin Gem Lab,
Lucerne, Switzerland, spoke about global sources of corundum, while Thomas Hainschwang of GGTL Laboratories,
Balzers, Lichtenstein, discussed their efforts to trace emeralds
through observation, chemical composition, and spectroscopy.
Copies of some of the presentations delivered at the conference are available on the ICA website (visit www.gemstone.org, and click on ICA Congress 2011 under Quick
Links).
Robert Weldon (rweldon@gia.edu)
GIA, Carlsbad
Scottish Gemmological Conference 2011. This four-day
SGA event was held in Perth, Scotland, on April 29May 2
with more than 50 delegates in attendance. The first lecture, by Dr. Marcia Pointon (University of Manchester,
U.K.), addressed the depiction of geologic features and
mineral specimens by 19th century British artists.
Two lectures on alexandrite were given by Dr. Karl
Schmetzer (Petershausen, Germany). The legend of alexandrite being discovered the same day that Russian crown
prince Alexander came of age seems to be false, as records
show it was found a year earlier. Historically, alexandrite
production in Russia was a byproduct of emerald mining,
and the gem was not considered important. The color
change of alexandrite is best described as going from
bluish green to purplish red. Stones showing a color
change without a red component should simply be
described as color-change chrysoberyl.
Alan Hodgkinson (SGA president, Edinburgh), discussed issues surrounding specific gravity testing.
Traditional heavy liquids such as bromoform, methylene
iodide, and Clerici solution are all toxic. A safer and more
versatile liquid is sodium polytungstate (SG 2.9), which is
water-soluble and also has a specific gravity that corresponds directly to its refractive index. Thus, if the liquid is
adjusted so that a stone remains suspended, a drop of that
254
liquid can be placed on a refractometer to determine the

stones RI. When working with mounted stones, RI can be
determined from the point at which a stone disappears
in the liquid. With traditional hydrostatic weighing, the
use of pure water at 4C and taking readings to at least two
places to the right of the decimal point are important.
Dominic Mok (Asian Gemmological Institute &
Laboratory, Hong Kong) discussed the laboratory situation
in the Far East. There are now more than 20 labs in Hong
Kong, as well as increased competition from China. Prices
for services have fallen substantially, and customers are
insisting that more advanced testing such as EDXRF analysis be shown on reports. Due to insurance considerations,
more-expensive items cannot be kept overnight, so sameday service is required.
Market trends were addressed by Stuart Robertson
(Gemworld International, Glenview, Illinois). Economic
recovery is slow in the U.S. and Europe, while the Far East
markets continue to be strong. Blue sapphire is still the
best seller, with ruby drawing very high prices for extra
fine color, and the emerald market is improving as a result
of greater consumer acceptance of treatments and an
increase in supply. Color substitutions are commonly
being used to provide lower-cost alternatives (e.g., rubellite
tourmaline and spinel instead of ruby, and apatite instead
of Paraba tourmaline). Treatments are creating a category
best described as Fashion Accessories, and such stones
cannot be promoted as rare.
David Callaghan (retired jeweler, London) discussed
the use of nature motifs in jewelry. He showed examples
of flowers, insects, and animals that were depicted with
gemstones or materials such as enamel and Bakelite.
In the closing two days, delegates had the option to
attend various workshops and tour the mineral collection
on display at the National Museum of Scotland in
Edinburgh.
Douglas Kennedy (douglas@gialondon.co.uk)
GIA, London
Sinkankas Diamond Symposium 2011Diamond. The
ninth annual symposium in honor of John Sinkankas took
place April 16 at GIA in Carlsbad. Co-hosted by GIA and
the San Diego Mineral and Gem Society, the sold-out
event was attended by 132 people.
After opening remarks by convener Roger Merk
(Merks Jade, San Diego, California), Scott Sucher (The
Stonecutter, Tijeras, New Mexico) reviewed the fascinating history of diamond cutting up to 1750. The first record
of diamond being made was in 1280 AD, when stones
were point cut by grinding them on an iron plate with
diamond grit. Major breakthroughs came with the development of the scaife in the 1400s and wire saws in the
1600s. Al Gilbertson (GIA, Carlsbad) continued with diamond cutting after 1750, following the development of the
brilliant cut with contributions by John Mawe, Henry
Morse, and Marcel Tolkowsky. In contemporary times, we
GEMS & GEMOLOGY
FALL 2011
have seen the development of laser cutting, proportion

viewers, and automated scanners that provide a variety of
possibilities for cutting rough into various fancy shapes.
Dr. James Shigley (GIA, Carlsbad) reviewed the geology and exploration of diamond deposits. An economic
kimberlite pipe typically has a grade of only one part diamond per 1 million parts host rock (0.0001% by volume).
Dr. William Skip Simmons (University of New Orleans)
focused on diamonds crystal structure and mineralogy.
Due to its high density, diamond has the highest RI of any
natural colorless transparent material.
Dr. Sally Eaton-Magaa (GIA, Carlsbad) reviewed the
production of synthetic diamond by chemical vapor deposition (CVD) and high pressure, high temperature (HPHT)
growth techniques. For the latter process, it takes about 80
hours to grow a 3.5 ct crystal. Dr. Christopher (Mike)
Breeding (GIA, Carlsbad) explained how treatments such
as irradiation and heating (with or without accompanying
high pressure)and various combinations thereofcan
change the color of diamond based on the characteristics
of the starting material. For example, HPHT processing of
type Ia pale yellow starting material containing nitrogen
pairs can form defects consisting of isolated nitrogen
atoms that are then irradiated and annealed to produce NV
centers, which give rise to red coloration. Dr. George
Rossman (California Institute of Technology, Pasadena)
examined the causes of coloration in diamond. While the
mechanisms involved in producing the color of yellow,
blue, green, brown, and black stones are known, the color
origin of blue-gray-violet, red-pink, and chameleon diamonds is not well understood.
Meg Berry (Mega Gem, Fallbrook, California) described
her experience with diamond drills for processing and
carving gem materials. She favors a 0.75-mm-diameter bit
that is sintered with diamond particles, rather than being
CVD coated. John Koivula (GIA, Carlsbad) illustrated the
microworld of diamond, and emphasized that mineral
inclusions are actually quite rare, with fissures/feathers
and graphite being much more common. Certain mineral
inclusions are indicative of a diamonds source rock, such
as chromite (peridotite), omphacite (eclogite), and
moissanite (deep mantle paragenesis).
Each attendee received a two-volume handout with
presentation summaries as well as outside contributions;
additional copies are available from Mr. Merk ($25 + shipping; merksjade@cox.net). Next years Sinkankas symposium will take place April 21, and the theme will be topaz.
Brendan M. Laurs
MISCELLANEOUS
A jewel that survived 9/11. September 11, 2011, marked
the 10-year anniversary of the terrorist attacks on New
York and Washington, DC. In the aftermath of the New
York attacks, a nine-story office building adjacent to
the twin towers, 5 World Trade Center, partially collapsed but remained standing. The structure was ulti-
mately demolished in January 2002. Buried under tons

of rubble inside the building were 2,500 safety deposit
boxes in the vault of a JPMorgan Chase branch. The
vault sustained severe damage from the fires that
burned for several days after the attacks.
The melted and semi-fused safety deposit boxes were
subsequently moved as a unit to the basement of One
Chase Manhattan Plaza. In early 2002, the bank began
meeting with box owners to return any remaining contents. Charles Maikish, a JPMorgan Chase official, told the
New York Daily News that workers had found mostly
ashes in the boxes: The only thing that would have survived was metal or stone.
Los Angeles gem specialist Robin Silvers recently
brought to this contributors attention a piece of jewelry
that survived the disaster in one of these deposit boxes, a
1950s-era 14K white gold ribbon bow brooch (figure 50). A
client of hers was hoping to restore the brooch. The
clients father had recovered it with a few other jewelry
articles during the very last appointment for retrieving
possessions. The insurer had an appraisal done and
returned the jewelry six months later.
This contributors examination showed the following:
The brooch measured 49.85 31.00 mm and contained 75
diamonds (2.78 carats estimated total weight) in a variety
of cuts and settings, consisting of eight prong-set round
brilliants, 41 bead-set round single cuts, seven prong-set
marquise cuts, and 19 channel-set baguettes. It was missing one diamond (apparently lost before the terrorist
attack). The metalwork was blackened, but remarkably
the diamonds were in good condition and did not show
any significant signs of degradation.
The client ultimately decided not to restore the piece,
preferring instead to keep the brooch in its present condition so people can reflect on the ironic beauty of this
blackened jewel that survived the tragic September 11
attacks.
David Humphrey (dhjewels@earthlink.net)
Gallery of Rare Jewels, Pacific Palisades, California
Update on Myanmar gem sales and production. The
Myanma Gem Emporium conducted a special sale of
jadeite, cultured pearls, and other gems July 313, 2011.
According to an article in Working Peoples Daily (July 15,
2011, pp. 9, 16), a total of 22,317 lots of jade were offered,
of which 17,449 sold. Of those, 17,222 lots sold by tender
and 227 by competitive bidding. Attendance and buying,
especially from China, was up from previous sales. On
average, jade lots sold at 343% of reserve prices. A total of
38 lots of other gems were sold, and cultured pearls also
were popular among buyers.
Production of jadeite in Myanmar remains strong,
while figures reported for other gem materials show variable trends (see table 1).
U Tin Hlaing
Dept. of Geology (retired)
Panglong University, Myanmar
GEMS & GEMOLOGY
FALL 2011
255
TABLE 1. Production of jadeite and other gems

in Myanmar, 20052010.
Year
20052006
20062007
20072008
20082009
20092010
Jadeite
(tons)
Ruby
(carats)
Sapphire
(carats)
Spinel
(carats)
Peridot
(carats)
20,005
20,458
20,266
32,921
25,795
2,298,413
1,555,596
1,518,854
1,821,085
1,692,587
428,891
715,160
308,642
1,234,596
1,081,773
833,218
925,050
363,260
429,312
125,755
344,471
732,442
583,215
21,160
ite (p. 119), the caption should have read as follows:

Heating of zoisite produced little to no change in
V3+ absorptions. A shift in the absorption edge was
recorded along the alpha pleochroic direction,
while additionally along the beta direction a band
at 375 nm became apparent. The most significant
change took place along the gamma direction,
where the shift in the absorption edge revealed
another band at ~380 nm, and the combined
removal of the 455 nm band created a transmission
window in the blue region of the spectrum. This
caused the pleochroic hue to change dramatically
from a brown-yellow or brownish greenish yellow
to slightly greenish blue.
Figure 50. This white gold and diamond brooch

(49.85 31.00 mm) was recovered from a melted
safety deposit box at the World Trade Center site
that was devastated by the September 11, 2001,
terrorist attacks. The metalwork is blackened,
but the diamonds are in good condition. Photo
by Robert Weldon.
ERRATA
Gems & Gemology regrets two incorrect figure captions
in the Summer 2011 Symposium Proceedings issue.
1. In the abstract by C. P. Smith, Natural-color tanzan-
2. In the abstract by S. Gumpesberger, Extreme conoscopy (p. 147), the caption should have read as follows:
An array of mini-sized spheres shows multiple
uniaxial figures across the entire surface of the
twinned amethyst slab on the left. The ametrine
slab on the right exhibits typical uniaxial figures in
Brazil law-twinned zones as well as uniaxial bullseye figures in untwinned areas. Amethyst can also
exhibit twinned and untwinned zones in the same
crystal. Photo by S. M. Gumpesberger; specimens
courtesy of the Royal Ontario Museum, Toronto,
Canada.
We thank Mr. Smith and Ms. Gumpesberger for bringing these corrections to our attention.
For online access to all issues of GEMS & GEMOLOGY from 1981 to the present, visit:
store.gia.edu
256
GEMS & GEMOLOGY
FALL 2011
SpringWinter 2010
Spring 2007
Pink-to-Red Coral: Determining Origin of Color
Serenity Coated Colored Diamonds
Trapiche Tourmaline from Zambia
Summer 2007
Global Rough Diamond Production since 1870
Durability Testing of Filled Diamonds
Chinese Freshwater Pearl Culture
Yellowish Green Diopside and Tremolite from
Tanzania
Polymer-Impregnated Turquoise
Fall 2007
The Transformation of the Cultured Pearl Industry
Nail-head Spicule Inclusions in Natural Gemstones
Copper-Bearing Tourmalines from New Deposits
in Paraba State, Brazil
Type Ia Diamond with Green-Yellow Color Due to Ni
Winter 2007
Latest CVD Synthetic Diamonds from Apollo
Diamond Inc.
Yellow Mn-Rich Tourmaline from Zambia
Fluorescence Spectra of Colored Diamonds
An Examination of the Napoleon Diamond Necklace
Spring 2008
Copper-Bearing (Paraba-type)
Tourmaline from Mozambique
A History of Diamond Treatments
Natural-Color Purple Diamonds from Siberia
Summer 2008
Emeralds from Byrud (Eidsvoll), Norway
Creating a Model of the Koh-i-Noor Diamond
Coated Tanzanite
Coloring of Topaz by Coating and
Diffusion Processes
Fall 2008
Identification of Melee-Size Synthetic
Yellow Diamonds
Aquamarine, Maxixe-Type Beryl, and
Hydrothermal Synthetic Blue Beryl
A New Type of Synthetic Fire Opal:
Mexifire
The Color Durability of Chocolate Pearls
Winter 2008
Color Grading D-to-Z Diamonds at the GIA
Laboratory
Rubies and Sapphires from Winza, Tanzania
The Wittelsbach Blue
Spring 2009
The French Blue and the Hope: New Data
from the Discovery of a Historical Lead Cast
Gray-Blue-Violet Hydrogen-Rich Diamonds
from the Argyle Mine
Hackmanite/Sodalite from Myanmar and
Afghanistan
Pink Color Surrounding Growth Tubes and
Cracks in Tourmalines from Mozambique
Identification of the Endangered Pink-to-Red
Stylaster Corals by Raman Spectroscopy
Summer 2009
Celebrating 75 Years of Gems & Gemology
The Type Classification System of Diamonds
Spectral Differentiation Between Copper and Iron
Colorants in Gem Tourmalines
Andalusite from Brazil
Peridot from Sardinia, Italy
Fall 2009
Characterization of Green Amber
Crystallographic Analysis of the
Tavernier Blue
Fluorescence Cage: Visual Identification
of HPHT-Treated Type I Diamonds
Ammolite Update
Polymer-Filled Aquamarine
Yellow-Green Hayne from Tanzania
Aquamarine from Masino-Bregaglia Massif, Italy
Winter 2009 (PDF only)
Ruby and Sapphire Production and Distribution:
A Quarter Century of Change
Cutting Diffraction Gratings to Improve
Dispersion (Fire) in Diamonds
Chrysoprase and Prase Opal from Haneti,
Central Tanzania
Demantoid from Val Malenco, Italy
Spring 2010
Strongly Colored Pink CVD Lab-Grown
Diamonds
Color Alterations in CVD Synthetic Diamond
with Heat and UV Exposure
Possible Sister Stones of the Hope Diamond
Confocal Micro-Raman Spectroscopy
Bastnsite-(Ce) and Parisite-(Ce) from Malawi
Summer 2010
The Wittelsbach-Graff and Hope Diamonds:
Not Cut from the Same Rough
Play-of-Color Opal from Ethiopia
A New Type of Composite Turquoise
Fire Opal from Madagascar
X-ray Computed Microtomography
Applied to Pearls
Hibonite: A New Gem Mineral
Fall 2010
An Era of Sweeping Change in Diamond and
Colored Stone Production and Markets
Gem Localities of the 2000s
Gemstone Enhancement and Its Detection
in the 2000s
Developments in Gemstone Analysis Techniques
and Instrumentation During the 2000s
Winter 2010
Synthetic Gem Materials in the 2000s
Yellow Scapolite from Madagascar
Pietersite from Namibia and China
Update on Mexifire Synthetic Fire Opal
Gems in a Ciborium from Einsiedeln Abbey
For a complete list of articles fr om 1981 forward, visit gia.edu/gandg.
Now Available
Online:
All Articles
and Issues 19812011
Get PDF Articles at
gia.metapress.com
Electronic (PDF) versions of all articles fr om
Spring 1981 forward are available as part of
Gems & Gemology Online.
Order Back Issues (Print and PDF)

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10% discount for GIA Alumni and active
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The Book Reviews and Gemological Abstracts sections are provided in the online (PDF) version of the journal. Below are the
titles of the books and articles reviewed, with the reviewers names indicated in brackets. These sections are available free of
charge both on the G&G website (gia.edu/gandg) and as part of G&G Online (gia.metapress.com), and are paginated separately from the rest of the issue.
Book Reviews
Living Jewels: Masterpieces from Nature. By Ruth Peltason,
2010 [Delphine A. Leblanc]
The Extraordinary World of Diamonds. By Nick Norman, 2010
[A. J. A. Bram Janse]
The Workbench Guide to Jewelry Techniques. By Anastasia
Young, 2010 [Doug Canivet]
World Hallmarks, Volume I: Europe, 19 th to 21 st Centuries,
2nd ed. By William Whetstone et al., 2010 [Jo Ellen Cole]
Mineral Treasures of the World. By The Geological Museum of
China and The Collectors Edge Minerals, 2010 [Michael T. Evans]
Gemological Abstracts
COLORED STONES AND ORGANIC MATERIALS
A survey of Mn-rich yellow tourmaline from worldwide localities and implications for the petrogenesis of granitic pegmatites. By W. B. Simmons et al. [James E. Shigley*]
DIAMONDS
Alluvial diamond resource potential and production capacity
assessment of the Central African Republic. By P. G. Chirico
et al. [James E. Shigley*]
assessment of Ghana. By P. G. Chirico et al. [James E. Shigley*]
assessment of Mali. By P. G. Chirico et al. [James E. Shigley*]
Brown diamonds from an eclogite xenolith from Udachnaya
kimberlite, Yakutia, Russia. By A. S. Stepanov et al. [Guy Lalous*]
Spectroscopic and microscopic characterization of color lamellae
in natural pink diamonds. By E. Gaillou et al. [James E. Shigley*]
Trace-element patterns of fibrous and monocrystalline diamonds:
Insight into mantle fluids. By S. Rege et al. [Kyaw Soe Moe*]
GEM LOCALITIES
Geochemical and geological controls on the genesis of gemquality Paraba tourmaline in granitic pegmatites from
northeastern Brazil. By H. Beurlen et al. [James E. Shigley*]
The history of kunzite and the California connection. By M.
Mauthner [Keith A. Mychaluk*]
Lopale du Wollo, Ethiopie: Des mines de gisement! [Opal
from Wollo Ethiopia: A source of mining capacity!] By F.
Mazzero et al. [Guy Lalous*]
Prediction of exploration target areas for gem deposits in
Mogok Stone Tract, northern Myanmar, by integrating remote
sensing and geoscience data. By T. K. Oo [James E. Shigley*]
Rubis et saphirs de Marosely, Madagascar [Ruby and sapphire
from Marosely, Madagascar]. By L. E. Cartier [Guy Lalous*]
Sapphires from Sri Lanka. By T. Waltham [Annette Buckley*]
INSTRUMENTS AND TECHNIQUES

Test visuel sur lattraction magntique des matires gemmes
[Visual test of the magnetic attraction of gemstone materials].
By T. Pradat and J.-P. Gauthier [Rolf Tatje*]
Three-dimensional X-ray radiography. By T. Hainschwang

[Kyaw Soe Moe*]
JEWELRY HISTORY
Brazilian colored gemstones in historical jewelry. By R.
Galopim de Carvalho [Jo Ellen Cole*]
Hippologie arabe et archogemmologie sur un harnachement
mameluk, 2me Partie [Arab hippology and archaeological gem ology on a Mamluk harness Part 2]. By E. Gonthier et al. [ Guy
Lalous*]
Hippologie arabe et archogemmologie sur un harnachement
mameluk, 3me Partie. By E. Gonthier et al. [Guy Lalous*]
Gemme da Vigna Barberini (Colle Palatino, Roma) [Gem stones
from Vigna Barberini (Palatine Hill, Rome)]. By E. Gliozzo et al.
[Rolf Tatje*]
Non-destructive analysis of amber artefacts from the prehistoric
Cioclo vina hoard (Romania). By E. S. Teodor [ Edward R.
Blomgren*]

Crystal growth and perfection of large octahedral synthetic diamonds. By A. F. Khokhryakov et al. [Jennifer Stone-Sundberg*]
Developments of elemental technologies to produce inch-size
single-crystal diamond wafers. By H. Yamada et al. [ Jennifer
Stone-Sundberg*]
TREATMENTS
Discrimination between natural and HPHT-treated type IIa
diamonds using photoluminescence spectroscopy. By H. J.
Lim et al. [James E. Shigley*]
Nouvelle absorption utile la dtection des diamants traits par
irradiation et chauffage: Le triplet 6021, 6070 et 6139 cm 1 [New
absorption useful in detecting diamond irradiation and annealing
treatment: A triplet at 6021, 6070 and 6139 cm1]. By A. Respinger
[Guy Lalous*]
MISCELLANEOUS
2010: Year of replenishment, speculation and recycling. By C.
Even-Zohar [Edward Johnson*]
Blood diamonds: International policy options for conflict resolution. By S. Lahiri [Russell Shor*]
Diamonds without borders: An assessment of the challenges
of implementing and enforcing the KP Certification Scheme.
By Partnership Africa Canada [Edward Johnson*]
Environmental stewardship in gemstone mining: Quo vadis?
By L. Cartier [Edward R. Blomgren*]
Gemstone mining as a development cluster: A study of Brazils
emerald mines. By J. Puppim de Oliveira and S. Ali [ Edward R.
Blomgren*]
The geoheritage significance of crystals. By M. Brocx and V.
Semeniuk [Edward R. Blomgren*]
The Tucson mineral show and the market for collector minerals: The potential for artisanal and small scale miners. By B.
Ross et al. [Michele Kelley*]
* Member of the Gemological Abstracts Review Board
258
G&G ONLINE
GEMS & GEMOLOGY
FALL 2011
EDITORS
Susan B. Johnson
Jana E. Miyahira-Smith
Thomas W. Overton
Living Jewels:
Masterpieces from Nature
By Ruth Peltason, 224 pp., illus.,
publ. by The Vendome Press
[www.vendomepress.com], New
York, 2010. US$50.00
In a time of skyrocketing gold prices,
it is interesting to see organic materials such as leather, wood, amber, and
feather making a strong comeback in
the jewelry industry. Yet this new
trend is as old as jewelry itself. Peltason takes the reader on a thematic
journey to explore the variety of living jewels, traditional as well as
exotic. Organic materials are just as
challenging as minerals for gemologists, whether it concerns identification, treatment detection, disclosure,
or ultimately valuation. This book is
intended for jewelry amateurs and
professional dealers interested in
estate pieces, as well as jewelry
designers.
Lavishly embellished with more
than 350 color illustrations, Living
Jewels presents a vast selection chosen according to three main criteria:
originality, historical importance, and
the aesthetic prominence of the
organic material. It is therefore a subjective selection comprising famous
jewelry houses such as Van Cleef &
Arpels, Cartier, Tiffany, Boivin,
Belperron, Verdura, and Grima, while
also spotlighting contemporary jewelers such as Marguerite Stix, Patricia
Van Musulin, Ted Muelhing, and
Jennifer Trask. The book is well organized by material: amber, coral, horn,
ivory, pearls, shell, tortoise shell,
wood, and exotica.
Among the most noteworthy elements is a detailed 40-page section on
pearls. It features classical pearl jewelry such as Victorian fringe necklaces
as well as the most contemporary
BOOK REVIEWS
pieces such as the Queen Annes

lace pin by Ted Muehling. Also in
this section are coveted pearl treasures, including the late Elizabeth
Taylors Peregrina pearl and the socalled Baroda pearl necklace by
Cartier. Non-nacreous pearls such as
melo and conch are also discussed.
Two other sections of particular
interest deal with wood and exotica.
The wood section shows how this
versatile material, so prominent in
the decorative arts, is used by jewelers. A most welcome glossary on
selected varieties of wood provides
simple and useful descriptions for
identification. After highlighting Art
Deco and 1970s pieces, Peltason
reviews interesting works of contemporary studio artists such as Noma
Copley, Christine J. Brandt, Liv
Blvarp, and Anthony Roussel. She
features Lee Hale and Kiff Slemmons,
who use reclaimed everyday materials such as pencils and rulers. Equally
interesting is the exoticas section,
which displays the use of scarabs, butterflies, feathers, teeth, animal skins
(snakeskin and stingray), and even
various type of hair (elephant and
human). She also rekindles the memory of Harry Emanuel, an English
Victorian jeweler remembered for his
exquisite hummingbird ear pendants.
Peltasons elegant writing style is
one of the books main assets. One
might hope, however, for more content on this rich topic. For instance,
the materials are presented very succinctly, with room for more detailed
gemological content. The antique
jewels come with very little contextual information on art period, manufacturing techniques, and provenance.
Some of the jewelry in the exotica
section warrants more detailed ethnological explanation. The photos are
obviously of various sources and
reproduction quality, with different

magnifications often on the same
page. Unfortunately, this makes it
more difficult to evaluate the rarity
and quality of an individual piece.
This becomes particularly evident in
the pearl section, where assessing the
actual size of the jewelry and gemstones is a challenge, some pieces
being magnified and others minimized. Jewelry size information isnt
noted either.
Nevertheless, Living Jewels is an
elegant and interesting book for
antique jewelry enthusiasts, one that
explores a rich topic with a wide scope
of interest from 19th century jewelry
to the most cutting-edge creations.
DELPHINE A. LEBLANC
Hoboken, New Jersey
The Extraordinary World of

Diamonds
By Nick Norman, 302 pp., illus.,
publ. by Janaca Media
[janaca.co.za], Auckland Park,
South Africa, 2010. R199.96
The world of diamond is an extraordinary one indeed. The author has
made a brave attempt to outline this
world in 300 pages. The book is illustrated with many well-chosen
archival and contemporary photographs acquired from the Brentwood Library in Johannesburg, De
Beers, and various diamond mining
companies.
The first 40 pages give a summary
overview of where diamonds are
found, a history of their discoveries,
prospecting and mining methods, and
cutting and polishing. The next 150
pages discuss in greater detail the
development of discoveries from
ancient India, Brazil, and Venezuela,
GEMS & GEMOLOGY
FALL 2011
S1
to more recent times in South Africa

and the rest of the continent, Russia,
Canada, and Australia. Earlier narratives such as Legrands 1980 book
Diamonds: Myth, Magic and Reality
are used extensively, but for recent
developments the author has drawn
upon firsthand accounts from known
experts. Included are discussions of
the recently discovered diamond
mines in Canada, the Bunder prospect
in India, and the Argyle mine in
Australia.
The next 60 pages present a more
detailed account of modern exploration and mining, beginning with
criteria for area selection, defining
drill targets, and conducting feasibility studies. Also included are case histories of the alluvial deposits at Oena
in the lower Orange River, Verneukpan in Namaqualand, coastal and offshore deposits along the Atlantic, and
kimberlites in Botswana and Canada.
There is also a discussion of Cliffords
rule, kimberlite indicator minerals
(e.g., G10 garnet and the Gurney
Cr/Ca diagram), and the distribution
of carbon in the mantle and subducted crust. This is followed by a discussion of microdiamonds formed by
meteorite impact (exemplified by
Popigai in northern Siberia), microdiamonds found in meteorites, graphitized diamonds in the Ronda ultrabasic massif in southern Spain, and a
possible cosmic origin of carbonado.
This is followed by a chapter on
diamond deposits along the Atlantic
coast of South Africa and Namibia,
and how the diamonds traveled from
inland kimberlite deposits. This chapter seems a bit misplaced, as its content really belongs in the section on
case histories. A final chapter on the
supply chain discusses the Central
Selling Organisation and the breakup
of its single-channel marketing
pipeline in the wake of conflict diamonds and new mines in Australia
and Canada that were outside De
Beerss control.
The author effectively uses text
boxes to present short biographies and
specific subjects, and he tells the story
in clear language. There are some
S2
BOOK REVIEWS
lapses, though. In the glossary, for

instance, a diamantaire should be
defined as a trader in diamonds, not
just a cutter. The case history for the
discovery of Orapa should have linked
Gavin Lamont with Manfred Marx,
the young De Beers geologist who
actually discovered the mine by collecting soil samples on the site and
noting the large numbers of garnets in
them. And while the Popigai and
Ronda occurrences are mentioned,
the very large source of microdiamonds near Kokchetav in northern
Kazakhstan is omitted. There, diamonds are contained in Cambrian
metasediments that were deeply
buried and subsequently uplifted. In
contrast to Ronda, however, the tiny
diamonds were enclosed in garnet and
zircon crystals and thereby preserved
from graphitization.
It is the maps, which appear to
have been adapted from a simple atlas,
that let the book down. All nine maps
contain some mistakesmisplaced
symbols, misnamed or omitted occurrences, and inconsistent terminology
in the captions.
Overall, this is an interesting story
that should have been edited more
tightly, as the sequence of subjects
jumps around and parts are repetitive
(beach and offshore mining are discussed in three different sections in
the book). The first 40 pages are spent
summarizing the rest of the book, and
a detailed discussion of the subject
matter doesnt begin until page 60. In
a book that tries to cover the whole
world of diamonds in 300 pages, that
seems a waste of space. The book is
written as a story rather than a scientific text, so it falls between two
stools. It is not up to the standard of a
textbook on diamond geology, but at
the same time it is sometimes too
detailed for the interested layman
who would have to be well versed in
geology and geography to fully appreciate the text. Otherwise, it is a welltold story and a reasonably priced
book.
A. J. A. (BRAM) JANSE
Archon Exploration
Carine, Western Australia
The Workbench Guide to

Jewelry Techniques
By Anastasia Young, 320 pp., illus.,
publ. by Interweave Books
[www.interweave.com], Loveland,
CO, 2010. $34.95
In this meticulously prepared work,
Anastasia Young presents over a hundred jewelry making processes and
techniques, organized in a bench reference style. The book opens with a
contents section that goes beyond a
simple listing of topics and page
numbers. There is a technique file
that numbers all the methods
described and the relevant page numbers, making it simple to quickly
locate a specific topic. There are also
mini-indexes called finders strategically placed throughout the book.
As a result of this well-considered
structure, navigating the book is a
pleasure.
The first chapter opens with a
short piece on how to set up a small
workshop. The rest of the chapter is
about the tools and materials used to
make jewelry. As an unreformed toolaholic, I was delighted with this section. Each item was represented by a
small high-quality photograph of each
tool, the techniques it is used for, and
how it is used. I particularly liked the
fact that the author noted the skill
level required for each tool. Essential
tools for beginning goldsmiths were
also identified by a symbol to help
novices assemble a tool kit. The
materials section of the chapter gives
a broad overview of both traditional
and nontraditional materials used in
modern jewelry, ranging from gold to
concrete.
The second chapter is the heart of
the book. It begins with essential techniques that must be mastered, including sawing, filing, soldering, sanding,
and polishing; these become more
advanced as you go farther into the
chapter. Each technique is described
in some detail and then illustrated
using three or four photographs
accompanied by captions. The method is effective in conveying a basic
understanding. Jewelers who have
GEMS & GEMOLOGY
FALL 2011
mastered the core techniques should

be able to incorporate the more
advanced techniques into their own
projects using the examples provided.
Given the broad range of techniques the author describes, it would
be unfair to expect a lot of detailed or
highly technical information. The
section on chasing and repouss is
typical of her approach. Its four pages
cover three techniques, well de scribed and illustrated, with three
excellent photos of jewelry made
using the techniques and about a
dozen paragraphs discussing materials, tools, and the basic operations
involved. While she mentions that
chasing tools can be handmade by
the craftsman, she does not go into
the details of annealing, shaping,
hardening, and tempering them,
although she does point out the
necessity of these steps. Clearly, if
you want to master one of these techniques, you will need to look beyond
this book. On the other hand, if you
would like to try some of them out
and see how they apply to your work,
it is a great starting point.
The chapter ends with a section
on outwork. This section discusses
the kinds of work that might be contracted out to someone with ad vanced expertise or specialized equipment. Many books written about our
field mistakenly give the impression
that the craftsman should master
every technique and do it all. The
fact is that there have always been
specialists, and it is perfectly appropriate to send out work to someone
who can do it faster or better. The
jewelry industry is seeing the rapid
development of many highly technical and expensive processes, and none
of us has the time or capital required
to master it all. This section discusses
the kind of jobs that might be outsourced and contains many commonsense suggestions about how to work
with subcontractors to achieve good
results.
The third chapter is a brief 10
pages on design, including inspiration
and where to find it, sketching, and
technical drawing. I particularly liked
BOOK REVIEWS
the Design Checklist and the notion

of a brief to define and give structure to a project. The last section,
Design Realization, shows how to
convert drawings and concepts into
finished items. The idea of using
models or 3-D sketches made from
inexpensive or easily worked materials such as paper or modeling clay to
work out final shapes and solve
assembly problems is excellent. I was
impressed with the authors emphasis
on keeping detailed notes and drawings so that the sequence for constructing the piece has been worked
out before expensive materials and
labor are applied.
Next, the Going into Business
chapter covers a topic often omitted
in books of this type. In todays global
market, understanding the business
side of our craft has become more
important than ever. The first half of
the chapter covers photography and
promoting ones work. The author
has included a technique file that
shows how software can improve an
image, plus a brief discussion of the
difficulty in getting quality images of
jewelry. Her section on promotional
material is only one page, but it is full
of great ideas for communicating a
clear identity or brand to the world.
The balance of the chapter deals with
pricing jewelry and deciding where to
sell it and how to display it.
This book is very attractive;
almost every page has a photograph of
jewelry that relates to the text on that
page. The layout is pleasing and user
friendly, the text well written and
packed with good information. This is
a valuable book for students and
beginning goldsmiths, who will discover the broad range of techniques
and materials available today. Professional designers and goldsmiths
who seek innovative techniques or
materials to meet the changing
demands of todays jewelry market
will also find plenty of inspiration
here.
DOUG CANIVET
Gemological Institute of America
World Hallmarks, Volume I:

Europe, 19th to 21st Centuries,
2nd ed.
By William Whetstone, Danusia
Niklewicz, and Lindy Matula, illus.,
publ. by Hallmark Research Institute
[www.hallmarkresearch.com], San
Francisco, 2010. $228
This is a wonderfully organized volume that has long been needed by
appraisers, collectors, and museums.
The authors have a gift for taking this
very complex subject and making it
easily understandable.
The books 5S approach to identifying hallmarks stands for Strike,
Shape, Style, Standard, and System.
Strike is the actual stamping of an
impression onto a tested metal and
the resulting placement and quality of
that impression. The shape of the
mark is its outline, while the style
refers to its design and imagery. Standard marks indicate the fineness of a
particular metal. Lastly, the System of
sequential hallmarks involves the
mark image and the existence of a
surrounding frame with specific shape
and fineness numbers, sometimes
with a date number or letter.
The fifth S, System, also includes
four subcategories: Implied, Symbolic,
Inclusive, and Sequential (ISIS). In this
methodology, an implied hallmark is
recognized by the core image and/or
frame shape. These alone can indicate
type of metal, metal fineness, and
country or location of assay. A symbolic hallmark uses a formal or
national symbol representing the
assaying country but provides little
other information. A hallmark with
letters and numbers added to a core
image is considered an inclusive hallmark. The most informative and easily read hallmarks are sequential hallmarks, consisting of a series of marks
in a line or cluster.
The chapters that follow give a
brief history of the European hallmarking systems by country. The 5S system is applied, and a timeline of precious metal use in each country is provided. Additional hallmarks, along
with ancillary marks that serve a spe-
GEMS & GEMOLOGY
FALL 2011
S3
cific purpose, are described with assay

office marks and identification symbols.
In the back of the book is an analytical index containing a convenient
listing of hallmark images. Although
this image index does not include all
hallmarks, its orderly arrangement
makes looking for the image less
overwhelming than one might suppose. A historical timeline illustrates
various periods of political transition
for the countries that once formed the
Austro-Hungarian Empire, the Russian Empire and the USSR, and
Yugoslavia. The glossary of hallmark
terms is helpful in reading this book,
and an extensive bibliography completes the work. Companion volumes
featuring hallmarks of other countries
are in the works.
JO ELLEN COLE
Vista, California
Mineral Treasures of the World

By The Geological Museum of
China and The Collectors Edge
Minerals Inc., 125 pp., illus., publ.
by Geological Publishing House
[www.gph.com.cn], Beijing, 2010.
286
The Mineral Treasures of the
World exhibit opened in the summer
of 2010 during Chinas World Fair in
Shanghai. Cosponsored by the
Geological Museum of China and
The Collectors Edge Minerals, it
showcased many of the worlds greatest localities for fine minerals with
very rare and exquisite examples.
This book was written to accompany
the exhibition, while educating readers and serving as an infomercial for
The Collectors Edge.
The books Gallery of Treasures
section contains splendid color photographs of specimens from the exhibit. They are outstanding examples,
worthy of the finest collectionstreasures indeed! Each specimen is
described with its name, chemical
formula, size, and a brief narrative.
Many of these are gem species.
S4
BOOK REVIEWS
The books educational purpose

is accomplished by the first five
chapters. They cover the mining of
specimens, their trimming and
cleaning, identifying superb specimens, worldwide market trends, and
how to start collecting fine minerals.
These chapters are richly illustrated
with color photographs that accentuate the subject matter. They build a
strong case for collecting fine minerals, comparing them to fine works of
art that justify their high prices. The
effort and expense of their mining
and the careful cleaning and trimming necessary to bring out their
best are chronicled in the story that
follows one piece from mine to mineral cabinet. The criteria of excellence are given as a general guide to
help the reader recognize a fine mineral specimen and why it holds
greater value.
The book extols the virtues of
collecting and preserving fine minerals for their enjoyment and as an
investment, while also setting out on
its third purpose, to be an advertisement for The Collectors Edge
Minerals as a prime source for their
acquisition. In relating its care and
know-how, the company makes a
strong case for itself.
The Mineral Treasures of the
World exhibit ended in July 2010, but
this accompanying book stands as a
permanent record of its excellence.
Readers of Gems & Gemology, especially those who also collect minerals
or appreciate gem species in their natural finest forms, should enjoy this
book. Although it does mention that
some of these specimens are affordable, it should have elaborated on this
point, as most people only dream of
owning such a specimen, let alone an
entire collection of them. And while
The Collectors Edge is a great
resource, there are many other excellent dealers to choose from. With
these last few points in mind, this
book is highly recommended, especially for the beginner.
MICHAEL T. EVANS
Gemological Institute of America
OTHER BOOKS RECEIVED

Collectors Guide to Granite Pegma tites. By Vandall T. King, 96 pp.,
illus., publ. by Schiffer Publishing
[www.schifferbooks.com], Atglen,
PA, 2010, US$19.95
Collectors Guide to Silicate Crystal
Structures. By Robert J. Lauf, 96 pp.,
illus., publ. by Schiffer Publishing
[www.schifferbooks.com], Atglen,
PA, 2010, US$19.95
These works, volumes 8 and 9 of the
Schiffer Earth Science Monograph
series, review the formation and mineralogy of pegmatites and the crystallography of silicates, respectively.
Typical for the series, both books are
aimed at the educated collector rather
than the academic reader. Both are
also well illustrated, though the pegmatite volume curiously features several photos of Colombian emerald
and red beryl, neither of which form
in pegmatites.
TWO
Gems and Gemology in Pakistan.
By Tahseenullah Khan and Allah
Bakhsh Kausar, 231 pp., illus., publ.
by Geological Survey of Pakistan
(www.gsp.gov.pk), Quetta, 2010, Rs.
3000. This special publication by the
Geological Survey of Pakistan reviews
the exploration, mining, manufacturing, and marketing of gem materials
from that country.
TWO
Diamond Math. By Kenneth A. Glas ser, 451 pp., illus., publ. by Kenneth
A. Glasser Co. [www.diamondmath.
com], Las Vegas, 2010, US$75.00.
This pocket-sized handbook contains
a set of charts allowing quick estimation of a diamonds weight based on
its external measurements. Separate
charts are provided for rounds and a
wide variety of fancy cuts.
TWO
GEMS & GEMOLOGY
FALL 2011
EDITORS
Brendan M. Laurs
Thomas W. Overton
GIA, Carlsbad
REVIEW BOARD
Edward R. Blomgren
Owls Head, New York
Annette Buckley
Austin, Texas
Jo Ellen Cole
Vista, California
R. A. Howie
Royal Holloway, University of London
Edward Johnson
GIA, London
Michele Kelley
Monmouth Beach, New Jersey
Guy Lalous
Academy for Mineralogy, Antwerp, Belgium
Kyaw Soe Moe
GIA, New York
Keith A. Mychaluk
Calgary, Alberta, Canada
Joshua Sheby
New York, New York
James E. Shigley
GIA, Carlsbad
Russell Shor
GIA, Carlsbad
COLORED STONES AND

ORGANIC MATERIALS
A survey of Mn-rich yellow tourmaline from worldwide localities and implications for the petrogenesis of granitic pegmatites. W. B. Simmons [wsimmons@uno.edu], A. U.
Falster, and B. M. Laurs, Canadian Mineralogist, Vol. 49,
No. 1, 2011, pp. 301319, http://dx.doi.org/10.3749/
canmin.49.1.301.
While yellow is an uncommon color for tourmaline, this variety has been found in certain granitic pegmatites in several
countries. The authors present electron microprobe data from
more than 200 yellow to yellow-green tourmalines from
Zambia, Madagascar, Russia, Mozambique, Nepal, the United
States, and Democratic Republic of Congo. The material is predominantly Mn-rich elbaite and fluor-elbaite (>3 wt.%
MnO), although rare yellow rossmanite and fluor-rossmanite
have come from Mozambique. Among the analyzed samples,
the MnO content ranged from 3.09 to 8.90 wt.%. No material
that could be classified as tsilaisite (>10.71 wt.% MnO) was
encountered. The analyzed samples also had higher TiO2 contents (averaging 0.28 wt.%) than pale-color tourmalines. The
yellow color is due to absorptions associated with the Mn2+Ti4+ intervalence charge-transfer mechanism. Yellow tourmaline is a rare late-stage magmatic to miarolitic cavitystage
mineral that requires specific conditions to form. Its presence
implies that the original pegmatite-forming melt is relatively
low in Fe and enriched in both Mn and B. During the early
stages of melt crystallization, Fe must be removed from the
system, but abundant Mn and B along with traces of Ti must
still be available during the late stages of pegmatite formation
for yellow tourmaline to crystallize.
JES
Elise Skalwold
Ithaca, New York
Jennifer Stone-Sundberg
Portland, Oregon
Rolf Tatje
Duisburg, Germany
Dennis A. Zwigart
State College, Pennsylvania
GEMOLOGICAL ABSTRACTS
This section is designed to provide as complete a record as

practical of the recent literature on gems and gemology. Articles
are selected for abstracting solely at the discretion of the section
editors and their abstractors, and space limitations may require
that we include only those articles that we feel will be of greatest
interest to our readership.
Requests for reprints of articles abstracted must be addressed to
the author or publisher of the original material.
The abstractor of each article is identified by his or her initials at
the end of each abstract. Guest abstractors are identified by their
full names. Opinions expressed in an abstract belong to the abstractor and in no way reflect the position of Gems & Gemology or GIA.
GEMS & GEMOLOGY
FALL 2011
S5
DIAMONDS
Alluvial diamond resource potential and production
capacity assessment of the Central African Republic. P. G. Chirico [pchirico@usgs.gov], F. Bar thlmy, and F. A. Ngbokoto, U.S. Geological
Survey Scientific Investigations Report 2010-5043,
Reston, Virginia, 2010, 22 pp.
Diamonds from what is now the Central African Republic
(CAR) were discovered almost a century ago, and commercial production began in 1931. The diamonds are recovered
along rivers that cut through sandstone formations in both
the Kadi-Mambr-Sangha region near Berberati, and the
Haute-Kotto region northeast of Bria. The country was
studied as part of an ongoing effort to assess world diamond production for the Kimberley Process certification
scheme. Because accurate production figures from the
CAR are not available, the authors used two indirect
methods to estimate diamond potential and production.
The methods took into account the size and grade of the
alluvial deposits, as well as the human resources engaged
in artisanal mining efforts. An estimated 39 million carats
of diamonds remain in these two regions, roughly twice
the countrys total output since 1931. Production capacity
is calculated at 840,000 carats per year, twice what has
been reported by the CAR government.
JES
Alluvial diamond resource potential and production capacity assessment of Ghana. P. G. Chirico [pchirico@
usgs.gov], K. C. Malpeli, S. Anum, and E. C. Phillips, U.S. Geological Survey Scientific Investigations Report 2010-5045, Reston, Virginia, 2010,
25 pp.
Diamonds were first found in the former Gold Coast
Colony (now Ghana) in 1919 along the Birim River near
the town of Abomoso, and commercial mining began
shortly afterward. There are no known kimberlite occurrences in Ghana. The two major alluvial diamond mining
areas are along the Bonsa River valley southwest of
Tarkwa, and the Birim River valley between the towns of
Akwatia and Oda. In both areas, diamonds are mined (usually by artisanal diggers) from gravel layers beneath the
alluvial flood plains and adjacent terraces. Based on careful
geological fieldwork, an estimated 91.6 million carats of
alluvial diamonds remain in these two areas.
JES
Alluvial diamond resource potential and production
capacity assessment of Mali. P. G. Chirico [pchirico@usgs.gov], F. Barthlmy, and F. Kon, U.S.
Geological Survey Scientific Investigations Report
2010-5044, Reston, Virginia, 2010, 23 pp.
Alluvial diamond deposits occur in Mali along river systems in the southwest portion of the country between the
S6
village of Kniba and the border of neighboring Senegal.

Some kimberlite pipes in the area have been identified, but
in most cases the primary sources of these diamonds are
unknown. Most have been found fortuitously by artisanal
gold washers. An interesting characteristic of diamonds
from the Kniba area is their exceptional sizenearly
15% of them weigh >15 ct. Crystals larger than 50 ct are
common, and the largest reported to date weighed 232 ct.
This report represents the results of a field study undertaken to assess Malis overall diamond potential. The
resource assessment focused on two alluvial mining areas,
Kniba and the nearby Bougouni region. The authors estimate that these two regions contain approximately 2.3
million carats of diamonds.
JES
Brown diamonds from an eclogite xenolith from
Udachnaya kimberlite, Yakutia, Russia. A. S. Stepa nov [aleksandr.stepanov@anu.edu.au], A. V.
Korsakov, O. P. Yuryeva, V. A. Nadolinniy, M. Perraki, K. De Gussem, and P. Vandenabeele, Spectrochimica Acta A: Molecular and Bio molecular
Spectros copy, Vol. 80, No. 1, 2011, pp. 4148,
http://dx.doi.org/10.1016/j.saa.2011.01.006.
Brown diamonds represent a significant proportion of global diamond production, and their economic importance
has encouraged intensive research on color enhancement
processes. The authors performed petrographic and spectroscopic studies of brown diamonds from an eclogite
xenolith from the Udachnaya pipe (Yakutia, Russia). A
thick plate was cut from the middle of the xenolith, from
which 19 thin sections were subsequently prepared. In
addition, diamonds were extracted from the xenolith and
their distribution was mapped. A polarizing microscope
was used to examine both the thin sections and the diamond crystals. Brown diamonds were randomly intermixed with colorless ones in the rock, often at the grain
boundaries of clinopyroxene and garnet.
Electron paramagnetic resonance, photoluminescence,
infrared, and Raman spectroscopy were used to identify
defects in the diamonds. The brown diamonds were characterized by a set of defects (H4, N2D, and a line at 490.7
nm), which is typical for plastically deformed diamonds
and indicates that they were likely annealed for a relatively short period after deformation occurred. The Raman
peak corresponding to graphite was not observed in brown
regions of the diamonds, eliminating the possibility that
graphite caused the coloration. Comparison with previous
reports of brown diamonds from eclogites showed that
the eclogitic sample had a typical structure, with no signs
of apparent deformation. Two mechanisms are proposed:
(1) deformation of the eclogite by external forces followed
by subsequent recrystallization of silicates, or (2) deformation by local stress arising from decompression and
expansion of silicates during the xenoliths ascent to surface conditions.
GL
GEMS & GEMOLOGY
FALL 2011
Spectroscopic and microscopic characterization of color

lamellae in natural pink diamonds. E. Gaillou
[gailloue@si.edu], J. E. Post, N. D. Bassim, A. M.
Zaitsev, T. Rose, M. D. Fries, R. M. Stroud, A.
Steele, and J. E. Butler, Diamond and Related
Materials, Vol. 19, No. 10, 2010, pp. 12071220,
http://dx.doi.org/10.1016/j.diamond.2010.06.015.
Some natural pink diamonds owe their coloration to multiple thin (~1 mm) pink lamellae oriented along octahedral
planes. Gemologists refer to these parallel colored lamellae
as a type of graining. The diamond is often nearly colorless between these lamellae, and stronger pink color is
associated with more numerous lamellae. Examination at
high magnification shows that the lamellae consist of
paired microtwins created by plastic deformation when
the diamond was under stress. The color of these diamonds results from a broad absorption band centered at
about 550 nm. The optical defect responsible for this broad
spectral feature was not identified, but it is likely associated with plastic deformation. Different optical defects were
identified spectroscopically within the lamellae (where
residual stress persists) and the intervening diamond. The
authors suggest that during plastic deformation, carbonatom vacancies are created in the diamond lattice during
twinning, and when these vacancies diffuse through the
lattice they tend to become trapped by nitrogen impurities
to form the new defect centers along the lamellae.
Annealing of plastically deformed brown diamonds can
result in a residual pink color that is stable under high
pressure and temperature conditions. The authors conclude that the deformation responsible for the pink color
in diamond occurred in the earths mantle. Similar lamellae causing the brown color of some diamonds probably
resulted from deformation during a more recent geologic
event, such as a rapid ascent to the surface in kimberlitic
or lamproitic eruptions.
JES
Trace-element patterns of fibrous and monocrystalline diamonds: Insight into mantle fluids. S. Rege, W. L.
Griffin [bill.griffin@mq.edu.au], N. J. Pearson, D.
Araujo, D. Zedgenizov, and S. Y. OReilly, Lithos,
Vol. 118, 2010, pp. 313337, http://dx.doi.org/
10.1016/j.lithos.2010.05.007.
The fluids in the earths mantle provide valuable information for understanding complex metasomatic processes.
These fluids can be trapped inside a diamond during its
formation in the cratonic subcontinental lithospheric
mantle. The trace-element patterns of 538 fibrous and
monocrystalline diamonds from deposits worldwide were
measured and analyzed using LA-ICP-MS.
In the fibrous diamonds, trace-element concentrations
varied irregularly within each stone, so no obvious chemical zoning was observed. There were two groupsthose
rich in K-Rb-Ba and those poor in Ba-Rb-K. Rock-forming
elements such as Al, Ca, Mg, K, Fe, and Ti showed positive correlations with each other, although this could not
be easily related to petrogenetic processes. Therefore,

these elements represented the fluids trapped during diamond formation. The chemical patterns observed in the
fibrous diamonds were broadly similar to those seen in
kimberlites and carbonatites.
Peridotitic monocrystalline diamonds were classified
into two groups. The first showed a higher trace-element
content but a negative anomaly in Ce, Y, and Sr. The second group had lower trace-element concentrations, while
Yb, Lu, Ba, and Rb were below the limit of detection.
Chalcophile elements, such as Pb, Cu, Zn, Co, and Ni
also were detected, representing submicroscopic sulfide
inclusions. Eclogitic monocrystalline diamonds were also
divided into two groups. The major rock-forming elements, such as Na, Fe, Mg, and Al, were present in these
diamonds, while chalcophile element contents were low.
Interestingly, the trace-element patterns of both peridotitic and eclogitic diamonds from a single source were
similar. The authors propose the existence of immiscible
high-density fluids/melts within the diamond stability
field (6 GPa and 12001300C). According to this model,
most peridotitic and eclogitic monocrystalline diamonds
likely crystallized from fluids such as the high-density
hydrous-silicic fluids related to the precipitation of
fibrous diamond.
Although diamonds of subduction origin did not contain rock-forming elements, they did show similar patterns of other elements. Thus, they were formed from
broadly similar high-density fluids. Diamonds of
superdeep origin (from the transition zone to the lower
mantle) had patterns similar to those of other monocrystalline diamonds around the world, except those from
Brazil, in which Al was the only rock-forming element
detected. A direct link between diamond-forming fluids
and pyrope, the most important diamond indicator mineral, was also found by analyzing trace-element patterns.
The diamond growth rate and environment may be closely related. In other words, diamond grows more slowly in
silicate-rich fluids, and consequently fewer fluid inclusions are trapped.
KSM
GEM LOCALITIES
Geochemical and geological controls on the genesis of
gem-quality Paraba tourmaline in granitic pegmatites from northeastern Brazil. H. Beurlen
[beurlen@ufpe.br], O. J. M. de Moura, D. R. Soares,
M. R. R. da Silva, and D. Rhede, Canadian Mineralo gist, Vol. 49, No. 1, 2011, pp. 277300,
http://dx.doi.org/10.3749/canmin.49.1.277.
Brazils famous neon blue Cu-bearing elbaite tourmalines occur in only four deposits of zoned and highly fractionated granitic pegmatites of the Borborema Pegmatitic
Province. Among several thousand barren pegmatites and
GEMS & GEMOLOGY
FALL 2011
S7
more than 750 Be-Li-Ta rare-metal pegmatites known in

this region, it is only in these four deposits (Batalha,
Capoeira, Glorious, and Quintos) that the necessary conditions were met for these tourmalines to form. The pegmatites are hosted by Fe-poor quartzite or metaconglomerate of the Equador Formation, and they are rich in Li minerals (mainly spodumene or lepidolite) and in B.
Significant amounts of schorl that crystallized in the border zone helped lower the Fe and Mg contents of the pegmatite-forming melt to allow the subsequent crystallization of Fe-poor elbaite. These pegmatites also show extensive replacement of feldspar and other primary minerals by
lepidolite.
The Cu-bearing tourmalines usually occur at the transition between an albite-rich inner intermediate zone and
the quartz core, where they form wedge-shaped crystals
arranged in fan-like, radial, or comb-textured aggregates.
In some cases, they are also found in crystal-lined cavities
in the center of the pegmatites. The tourmalines may be
strongly color zoned, with a pink to red core, a blue intermediate portion, and a green rim. They are distinguished
by relatively high Cu, Li, and F, low Mn and Mg, and near
absence of Fe. They formed by direct crystallization from
a pegmatite-forming melt during an early stage of formation of the quartz core. The crystals are often partially or
completely replaced by lepidolite except within the
quartz core. Several sources have been suggested for the
copper found in these tourmalines, such as skarns and
quartz veins containing Cu-sulfide minerals in the Jucurut Formation that underlies the Equador Formation, but
this question has not been fully answered.
JES
The history of kunzite and the California connection. M.
Mauthner [mmauthner@gmail.com], Rocks &
Minerals, Vol. 86, No. 2, 2011, pp. 112131.
Facts are often lost to history, but occasionally good detective work can bring back missing details and complete an
interesting story. Kunzite, the main gem variety of spodumene, is relatively new to commercial markets, dating
back to the early 1900s. Yet questions remain about when,
where, and by whom the first specimens were truly discovered. Detailed research has yielded a surprisingly
intriguing history that traverses a scientific rivalry, exotic
localities, and hardened prospectors. Equally noteworthy
are the articles historical photographs, many of which the
author has rephotographed from the originals. Although
heavily weighted toward Southern California discoveries,
the article provides a good summary of kunzite finds in
Brazil and Madagascar. Discussion of kunzite from
Afghanistan and Nigeria is limited.
KAM
Lopale du Wollo, Ethiopie: Des mines de gisement! [Opal
from Wollo Ethiopia: A source of mining capacity!]
F. Mazzero, C. Dsagulier, B. Rondeau, D. Ayalew,
G. Ezezew, T. Cenki, and E. Bekele, Revue de Gem-
S8
mologie a.f.g., No. 174, 2010, pp. 1420 [in French].

The article investigates the geologic conditions of gem
opal formation at Wegel Tena, in Ethiopias Wollo
Province. The deposit consists of a single horizontal layer
of weathered ignimbrite (a volcano-sedimentary rock of
rhyolitic composition, formed by the deposition of volcanic ash over a wide area) within a thick series of unaltered Oligocene ignimbrite. The opals contain very wellpreserved plant fossils, which show they formed in a sedimentary environment, most likely during a pause in the
volcanic succession.
Mining conditions at Wegel Tena are harsh and dangerous, and the workers have little knowledge of proper techniques. Their tools are limited to hammers, chisels, shovels, and pickaxes. Many fatal accidents occur due to collapsing tunnels or falls from cliffs. There is no shoring or
ventilation in the tunnels. During their visit, the authors
explained some basic safety rules to the miners and donated safety equipment. The deposit is very promising, as the
opalized layer is quite extensive and shows a high gem
opal content. Wegel Tena has the potential to become an
important opal deposit, provided that the mining becomes
more organized and professional.
GL
Prediction of exploration target areas for gem deposits in
Mogok Stone Tract, northern Myanmar, by integrating remote sensing and geoscience data. T. K.
Oo, Advances in Geosciences, Vol. 26, 2010, pp.
181198.
The region around Mogok in northern Myanmar has been
one of the worlds most famous gem-producing areas for
almost 400 years. Igneous and metamorphic rocks, including granites and pegmatites, gneisses, marbles, schists, and
quartzites, are the source for the ruby, sapphire, and other
gems that are found in both primary and secondary
deposits. Most economic gem mines are found either
along certain horizons in marbles or in skarns, as well as
in alluvial placers derived from these rocks. The overall
geology of the area is complex, with igneous rocks intruding into preexisting metasedimentary rocks, which are
folded and faulted on a regional scale. Remote sensing and
geoscience data have produced a map of promising target
areas for gem mineralization at locations where marbles
occur.
JES
Rubis et saphirs de Marosely, Madagascar [Ruby and sapphire from Marosely, Madagascar]. L. E. Cartier
[gemlab@ssef.ch], Revue de Gemmologie a.f.g., No.
175, 2011, pp. 913 [in French].
This article examines the eluvial corundum deposit
recently discovered at Marosely, in south-central Mada gascar. The material ranges from red to blue, and stones
are typically zoned, giving them an overall purple color.
FTIR spectra show the presence of 3160 and 3309 cm1
absorptions in the untreated corundum. The relevance of
these bands to the detection of heat-treated corundum is
GEMS & GEMOLOGY
FALL 2011
discussed. LA-ICP-MS data for chromophores in colorzoned samples are consistent with EDXRF spectroscopy.
Results for other trace-elements (i.e., concentrations of
<1000 ppm) proved less revealing. Further research using
other analytical methods is needed to advance the study of
the corundum origin.
GL
Sapphires from Sri Lanka. T. Waltham [tony@geophotos.
co.uk], Geology Today, Vol. 27, No. 1, 2011, pp.
2024.
Sri Lanka has long been famous for its sapphires, which
are found scattered in the soils of the countrys valley
floors. Half of the worlds sapphires weighing more than
100 ct hail from the Ratnapura region. Sri Lankas gem
deposits, mined for over 2,000 years, are best exploited
through small-scale, nonmechanized mining. Shallow
pits worked by only a few miners dot the forested area of
Ratnapura, and when the pits reach bedrock, they are considered mined out. Old pits are refilled with soil from new
adjacent pits. This article features excellent photos
accompanying detailed descriptions of the locals mining
processes.
Once the sapphires have been mined, they enter into a
low-key local trade. Buyers and miners do not sell from
formal stalls but instead gather around the local clock
tower to deal through trusted verbal transactions. The
country also has a significant (50,000+ people) cottage
industry of cutting and polishing stones.
The majority of Sri Lankan sapphires are pale, and
these are heat treated to darken their color. Sapphires are
far from the only gems produced in Sri Lanka; only a
quarter of its 3-million-carat annual production is sapphire. Other gems include spinel, aquamarine, garnet,
alexandrite, and zircon.
AB
INSTRUMENTS AND TECHNIQUES

Test visuel sur lattraction magntique des matires
gemmes [Visual test of the magnetic attraction of
gemstone materials]. T. Pradat and J.-P. Gauthier,
Revue de Gemmologie a.f.g., No. 175, 2011, pp.
1418 [in French].
Gems can show different types of magnetism (dia-, para-,
ferro-, antiferro-, and ferrimagnetism) depending on their
composition and the spin of certain elements they contain. This determines whether they are strongly or weakly
attracted to a magnet, or not at all. This behavior is easily
demonstrated with neodymium magnets, which are inexpensive and very strong. The authors describe three simple
methods (direct application, the floating technique, and
the pendulum method) for determining a gems magnetic
behavior. These can be applied as a quick test for presorting mixed lots of similar-looking stones (e.g., red garnets
and spinels, as illustrated). However, magnetism alone is
not sufficient for identifying a gem, and a samples identity
must always be corroborated by standard tests. The article

contains a useful, comprehensive list of gems and their
magnetic characteristics.
RT
Three-dimensional X-ray radiography. T. Hainschwang
[thomas.hainschwang@ggtl-lab.org], Gems & Jewellery, Vol. 20, No. 1, 2011, pp. 1114.
X-ray computed microtomography is the most sophisticated and effective method for 3D X-ray imaging, but it is
very costly and time-consuming. Thus the author developed a rapid, economical analytical method. Three-dimensional X-ray radiography was conducted using a tunable Xray tube, a digital X-ray sensor, and a high-precision rotation device.
The process involves recording multiple images to
obtain 3D radiographs, and these are processed using special software for higher contrast and sharpness. Each analysis requires 20 minutes, including sample preparation
and data processing. Extensive testing proved that this
system could identify and quantify dense filler substances
in gemstones, such as fissure-filled rubies and diamonds.
It also revealed the concentric structure of a natural pearl
from Pteria penguin, whereas conventional X-radiography
usually shows indistinct structure. Unfortunately, entire
pearl strands cannot be scanned by this method.
The 3D X-ray radiography system is cost-effective to
operate and maintain, and it is a faster method than X-ray
computed microtomography. Although its images do not
have such high resolution, they are far superior to conventional X-radiographs.
KSM
JEWELRY HISTORY
Brazilian colored gemstones in historical jewelry. R.
Galopim de Carvalho, InColor, No. 15, Fall/Winter
2010, pp. 4044.
Brazil is well known for its seemingly inexhaustible supply
of various gems from many areas of the country. But until
the discoveries of gold in Minas Gerais in the 17th century
and of diamonds in the mid-1720s, little was known of
Brazils stunning mineral wealth. When diamonds were
found near a town now called Diamantina, locals became
more aware of the mineral riches in the riverbeds and other
sedimentary deposits. During the second quarter of the
18th century, prospectors discovered what were initially
termed Brazilian rubies in the Ouro Preto area of Minas
Gerais. These turned out to be yellow, orange, pink, and
orangy red topaz, and they soon proved quite popular with
jewelers in Portugal, which still ruled Brazil. The trade
term Imperial topaz is thought to have originated soon
after the discovery of these deposits.
To enhance the apparent color of Brazilian gemstones,
colored foil was often placed under closed-back settings. In
the late 18th and early 19th centuries, colorless topaz was
widely used in silver jewelry. Several methods were
GEMS & GEMOLOGY
FALL 2011
S9
employed to make it resemble diamond, including painting the culet with black ink to simulate the extinction of
light in diamonds with a closed-back setting. In the late
1700s, huge quantities of colorless quartz were discovered
in Brazil, and the resulting gems also were set in Portuguese silver jewelry with closed backs and painted culets.
Pyrope-almandine and transparent yellow chrysoberyl
were also given the foil-back treatment to present a uniform color.
JEC
Hippologie arabe et archogemmologie sur un harnachement mameluk, 2me Partie [Arab hippology and
archaeological gemology on a Mamluk harness
Part 2]. E. Gonthier [gonthier@mnhn.fr], T. DeNoblet, and J.-P. Sage-Fresnay, Revue de Gemmologie a.f.g., No. 174, 2010, pp. 2730. Hippologie
arabe et archogemmologie sur un harnachement
mameluk, 3me Partie. E. Gonthier, T. De-Noblet,
and J.-P. Sage-Fresnay, Revue de Gemmologie a.f.g.,
No. 175, 2011, pp. 2227 [in French].
Part 2 of this series on the Mamluk harness (see abstract of
Part 1 in Spring 2011 G&G, p. S9) focuses on its dark blue
lapis lazuli and red coral, and the meaning of these colors.
Lapis was associated with the night and its myriad stars,
the sacred sanctuary of the pharaohs souls. Red coral was
prized for its rarity and its symbolic and traditional values.
The color red represented the desert, as well as blood, violence, and victory. The article also mentions the shipping
routes that brought these stones to Egypt.
Part 3 examines the harnesss turquoise and ruby.
Turquoise from Persia has a more stable color than its
Chinese counterpart, and the color quality of the turquoise
in the harness suggests a Persian origin. The ruby is evidence of the trade ties between the Far East and North
Africa. The caravans of the Silk Road brought the stones
first to Turkey and then to Egypt. It is difficult to identify
the exact origin of the ruby in the Mamluk harness,
though it could be of Afghan or Tajik origin. In the
Mamluk tradition, the role of precious metals and stones
complements the relationship between man and his horse.
The Arabian horse was ornately decorated not because its
rider was a lord, but because this breed was considered the
mount of the prophet.
GL
Gemme da Vigna Barberini (Colle Palatino, Roma)
[Gemstones from Vigna Barberini (Palatine Hill,
Rome)]. E. Gliozzo, N. Grassi, C. Meneghini, P.
Bonanni, and M. A. Tomei, Rivista Gemmologica
Italiana, Vol. 5, No. 3, 2010, pp. 185196 [in Italian].
The authors examined 25 gemstones found in archaeological excavations of Vigna Barberini, a 1st/2nd century AD
site at the Palatine Hill of Rome. Spatially resolved X-ray
diffraction, Raman spectroscopy, and PIXE measurements
were used to identify the stones, which included various
chalcedony and jasper varieties, almandine, peridot, and
lapis lazuli. In most cases, however, their geographic origin
S10
could not be determined. The approach used in this study

may help to establish discriminating criteria, which in
turn would allow the reconstruction of ancient trade
routes.
RT
Non-destructive analysis of amber artefacts from the prehistoric Cioclovina hoard (Romania). E. S. Teodor
[esteo60@yahoo.co.uk], E. D. Teodor, M. Virgolici, M.
Manea, G. Truica, and S. Litescu, Journal of Archaeological Science, Vol. 37, 2010, pp. 23862396,
http://dx.doi.org/10.1016/j.jas.2010.04.011.
Amber is well known from the Baltic Sea and the
Dominican Republic, but deposits are found around the
world, including Romania (referred to as Rumanite or
Romanite). The aim of this study was to determine if the
samples found in a Romanian archeological hoard came
from local deposits or from the shores of the Baltic Sea on
the Amber Route, which crossed central Europe.
Nondestructive analytical techniques are naturally
preferred for archeological artifacts. A total of 43 amber
bead fragments belonging to 13 different types according
to shape and color, dating from the transitional period
between the Late Bronze Age and the Iron Age, were analyzed by Fourier-transform infrared spectroscopyvariable
angle reflectance (FTIR-VAR) and Fourier-transform
Raman spectroscopy (FT-Raman) coupled with multivariate data analysis. Raman spectroscopy has been used in
the last decade to identify specific structural units or
functional groups in complex mixtures of fossil resins,
allowing quick and nondestructive provenance determination; this technique has also been used to identify and
explain chemical degradation mechanisms of Baltic
amber. The combination of the two analytical techniques
used in this study increases the accuracy of either technique alone, given the great similarities between Baltic
and Romanian amber.
The results strongly suggest that a large part of the
amber from the hoard had its origin in the Buz`u county
of Romania, not in the Baltic area, and thus had no connection to the Amber Route.
ERB

Crystal growth and perfection of large octahedral synthetic
diamonds. A. F. Khokhryakov [khokhr@uiggm.
nsc.ru], Y. N. Palyanov, I. N. Kupriyanov, Y. M.
Borzdov, A. G. Sokol, J. Hartwig, and F. Masiello,
Journal of Crystal Growth, Vol. 317, 2011, pp. 3238,
http://dx.doi.org/10.1016/j.jcrysgro.2011.01.011.
For this study, the authors produced 30 octahedral synthetic diamonds ranging from 0.4 to 3.5 ct using a highpressure, high-temperature (HPHT) technique. The crystals
were grown using a split-sphere (BARS) apparatus and a
Ni0.7Fe0.3 metal alloy catalyst. Growth conditions included
a temperature of 1550C and a pressure of 5.7 GPa. The
GEMS & GEMOLOGY
FALL 2011
largest crystal produced was 3.53 ct and had a maximum

width of 9 mm. Dislocation-free regions of about 58 mm3
and some dislocation-free {111} growth sectors were typical
for the larger crystals. The defects in these synthetic diamonds were studied using selective etching, double-reflection interference microscopy, infrared spectroscopy, and
other techniques such as X-ray topography, cathodoluminescence, and photoluminescence.
The carbon source was located above the growth zone.
Growth occurred as the carbon was deposited on the cooler central part, and convection rotated the melt upward
along the hotter exterior walls. The upper {111} faces were
preferred, with average growth rates of 3945 m per
hour. The resulting crystals exhibited low birefringence
and were generally inclusion-free and brownish yellow.
All of the synthetic diamonds exhibited nitrogen concentrations between 100 and 200 ppm, with the nitrogen in
the form of either C-centers (single substitutional atoms)
or A-centers (pairs of nitrogen atoms in neighboring substitutional positions). The degree of nitrogen aggregation
ranged from 5% to 60%, classifying them as types Ib+IaA
and IaA+Ib. X-ray topography studies on (110) plates cut
from the centers of the diamonds found that the synthetic
diamonds contained less than four bunches of defects
extending from the seed crystal. It was concluded that
single <111> dislocations result in low, wide growth
hillocks.
JS-S
Developments of elemental technologies to produce inchsize single-crystal diamond wafers. H. Yamada
[yamada-diamond@aist.go.jp], A. Chayahara, Y.
Mokuno, N. Tsubouchi, S. Shikata, and N. Fujimori, Diamond and Related Materials, Vol. 20,
2011, pp. 616619, http://dx.doi.org/10.1016/j.
diamond.2011.01.001.
Diamond offers many advantages over other semiconductor materials, such as a wide band gap and high thermal
conductivity. The availability of diamond wafers is therefore of great interest to the semiconductor industry.
Currently, three main factors limit the production of
these wafers: the difficulty of growing single-crystal synthetic diamond in suitable sizes at feasible growth rates,
the lack of sufficiently large seed crystals, and the materials brittleness.
The authors produced 1 inch (2.5 cm) mosaic synthetic diamond wafers based on the microwave plasma CVD
growth technique. Their process involved many clever
steps to enlarge a seed crystal and subsequently clone it.
Initially, enlargement was done by growth on various
faces. A lift-off process involving ion implantation facilitated cloning. Then, six half-inch seed clones were joined
to further widen the synthetic diamond wafer in the
desired orientation. Finally, clones of this mosaic wafer
were produced.
The mosaic wafer was examined with Raman spectroscopy at the junctions between seed crystal clones as
well as in non-junction areas. It was determined that the

full width at half maximum (FWHM) of the 1335 cm1
absorption is about 1.5 greater at the junctions than in
the non-junction areas. In all cases, the FWHM was less
than 5 cm1, a value better than that of synthetic diamond
grown hetero-epitaxially and near that of the HPHT-grown
type Ib substrate, but worse than that of high-quality
CVD-grown single-crystal synthetic diamond. The transmission of the mosaic wafers grown in this study showed
the cutoff wavelength to be between that of CVD type IIa
and HPHT type Ib synthetic diamond.
JS-S
TREATMENTS
Discrimination between natural and HPHT-treated type
IIa diamonds using photoluminescence spectroscopy. H. J. Lim, S. Y. Park, H. S. Cheong [hcheong@
sogang.ac.kr], H. M. Choi, and Y. C. Kim, Diamond
and Related Materials, Vol. 19, No. 10, 2010, pp.
12541258, http://dx.doi.org/10.1016/j.diamond.
2010.06.007.
Based on a study of 71 untreated type IIa diamonds (65
DF color, and six brown/M color) and 12 known-HPHTtreated stones, the authors presented spectroscopic criteria
for distinguishing between them. Photoluminescence
spectra were collected using 488 and 514.5 nm lasers, with
diamonds cooled in a liquid helium cryostat. Spectra were
collected on the six M-color diamonds both before and
after annealing. The authors reported that the loss of
brown color in these diamonds was minimal, which they
attributed to the heating conditions they could achieve
during the treatment (only up to 1800C for three hours).
The authors summarized changes in spectral features
(peak position and width, and the occurrence of peaks
with respect to one another) related to the GR1, NV, H4,
and H3 defect centers in both the untreated and treated
diamonds, and in the six diamonds that were annealed.
They proposed a discrimination scheme based on the presence or absence of specific PL spectral features, which they
claim provides strong evidence to distinguish untreated
and HPHT-treated colorless type IIa diamonds.
JES
Nouvelle absorption utile la dtection des diamants
traits par irradiation et chauffage: Le triplet 6021,
6070 et 6139 cm 1 [New absorption useful in
detecting diamond irradiation and annealing treatment: A triplet at 6021, 6070 and 6139 cm1]. A.
Respinger [axel.respinger@gemtechlab.ch], Revue de
Gemmologie a.f.g., No. 175, 2011, pp. 67 [in
French].
Samples of irradiated green diamonds were heated from
300C to 1100C in 50 increments to observe changes in
their infrared spectra. H1a, H1b, and H1c absorptions were
GEMS & GEMOLOGY
FALL 2011
S11
detected, as well as a previously undocumented triplet at

6139, 6070, and 6021 cm1. The triplet, which starts to
appear at 1000C, occurs mainly in type IaAB diamonds
but also in some type IaB diamonds. The feature seems to
be associated with B aggregates.
GL
MISCELLANEOUS
2010: Year of replenishment, speculation and recycling.
C. Even-Zohar, Idex, Vol. 26, No. 253, 2011, pp.
6573.
In the authors annual assessment of the diamond
pipeline, 2010 was characterized by three factors: replenishment of rough supply, recycling of polished goods, and
the return of diamond speculation. Due to the global economic downturn, 2009 saw the most severe financial contraction since World War II. But the trade managed it well
and avoided major bankruptcies. After the supply of rough
into the pipeline fell by about 50% in 2009, 2010 was a
year to restock, even if consumer demand had not yet
returned. Estimates for 2010 rough production were set at
125130 million carats, valued at US$11.8$12.2 billion.
That production figure was up from 2009 but still considerably down from the 160165 million carats produced in
2008. With a widening supply-demand deficit, rough prices
rose accordingly. Meanwhile, many looked for alternatives
to rough.
The year saw extensive recycling of previously owned
polished diamonds back into the markets, especially from
the U.S. into India. The author estimates that a global
total of 5.2 billion carats of diamonds have been mined,
worth about US$0.91.2 trillion in polished prices today,
and up to half of that is in American hands. He quotes
sources as using a widely accepted recycling price of 80%
below Rapaport. Global recycling has become an important part of the trade, estimated to be worth US$6 billion
in 2010.
The use of diamonds as an investment vehicle is once
again becoming a factor, mainly because of expected supply shortages.
EJ
Blood diamonds: International policy options for conflict
resolution. S. Lahiri [lahiri@siu.edy], Indian Growth
and Development Review, Vol. 2, No. 1, 2010, pp.
520, http://dx.doi.org/10.1108/17538251011035846.
The article develops a model, based on recent hostilities,
of how revenues from conflict diamonds, foreign aid, and
arms sales to warring nations make such conflicts worse
especially as foreign aid goes toward recruiting soldiers and
buying arms. The paper employs mathematical formulas
to model how controlling these factors could affect potential conflicts. The author concludes that taxing arms shipments and limiting them by international agreement are
S12
the most effective means of reducing the severity of conflicts.

RS
Diamonds without borders: An assessment of the challenges of implementing and enforcing the KP
Certification Scheme. Partnership Africa Canada,
November 2010, www.pacweb.org/documents/
diamonds_kp/diamonds_without_borders-nov2010_
eng.pdf.
Diamonds are notoriously easy to smuggle. Israel, as chair
of the Kimberley Process Certification System (KPCS) in
2010, recognized the importance of strengthening efforts
to combat diamond smuggling. This report by Partnership
Africa Canada, presented to the KPCS Plenary in
November 2010, details the work done by Israel, Canada,
and the U.S. to conduct multi-stakeholder consultations
in four West African countries: Guinea, Ivory Coast, Sierra
Leone, and Liberia.
Multilateral solutions were put forward such as collaboration between officials from key importing and
exporting countries, and mechanisms for greater information sharing. Also emphasized were national solutions
such as addressing the low prices offered to artisanal miners, which fuels the incentive to smuggle. Increased governance, including gathering of meaningful production
data and the use of law enforcement to bring smugglers to
justice, was also suggested.
EJ
Environmental stewardship in gemstone mining: Quo
vadis? L. Cartier [laurent.cartier@unibas.ch],
InColor, No. 15, Fall/Winter 2010, pp. 1219.
This article explores some of the complex relationships
between gems and the environmental ecologies from
which they are extracted. Although a number of large and
medium-scale companies are involved in colored stone
mining, artisanal miners represent 80% of the extraction
efforts. Protecting vulnerable ecologies is difficult when
artisanal miners do not share the same sense of environmental responsibility as the local people who depend on
the viability of the land. Just as often, regulation and
other government support for sustainability is limited or
nonexistent.
The author argues that all gem industry stakeholders,
including government agencies and consumers, must
examine and assume responsibility for the social, economic, regulatory, and environmental interrelationships that
constitute a sustainable approach to gem extraction. The
core sustainability question is this: Has the extraction left
a viable physical and social environment that can support
livelihoods in the long term once mining has ceased?
The author provides an excellent table summarizing
major environmental challenges associated with gem
mining. He specifies six domains (water, soil, air,
flora/fauna, human, and landscape), with 18 potential
GEMS & GEMOLOGY
FALL 2011
long-term consequences of mining and, most importantly, mitigation strategies. The article also discusses some
of the cultural, economic, and institutional variables that
undergird the continued lack of progress.
Twelve general recommendations to support responsible environmental stewardship and sustainability are
offered. These include realistic, cost-effective regulatory
mechanisms adapted to local realities, training, incentives, and practical assistance in cleaner production methods and the reclamation of mining sites.
ERB
Gemstone mining as a development cluster: A study of
Brazils emerald mines. J. Puppim de Oliveira and S.
Ali [japo3@yahoo.com], Resources Policy, Vol. 36,
j.resourpol.2010.10.002.
Using the concept of clusters and social upgrading, the
authors employ the case study method to analyze six
municipalities within the three most important emerald
producing regions in Brazil (the states of Goias, Minas
Gerais, and Bahia), in order to understand the numerous
social, economic, and policy dynamics of emerald mining
and its impact on local development. In this context, clusters are small agglomerations of economic agents working
in one specific sector in one region.
Most of the value-added economic benefits of emerald
mining have accrued to the top of the production chain,
which generally lies outside the mining region. In fact,
some specialists estimate that less than 5% of the retail
price of a good emerald remains at the local level. Because
most added value arises elsewhere, the local tax revenue
from mining is also small. Thus, the economic benefits of
emerald mining to local communities are minimal.
In many cases the mining activities also have caused
significant negative social impacts: increased strain on
public services and resources, greater crime, and health
and safety problems. The working conditions for miners
are notoriously poor: long hours, low wages, and dangerous mine conditions such as poor ventilation and extreme
heat. Workers also have, at best, informal contracts and no
benefits. The environmental impacts include deforestation, erosion, and soil and water pollution due, in large
part, to a lack of appropriate controls and technology.
Small-scale emerald mining may potentially create
favorable conditions conducive to longer-term development. Better cluster governance could harness the benefits
of scale and collective efficiency to overcome the main
obstacles to social development by upgrading through
markets, ethical concerns, and thoughtful regulation.
ERB
The geoheritage significance of crystals. M. Brocx, [geoheritage@iinet.net.au] and V. Semeniuk, Geology
Today, Vol. 26, No. 6, 2010, pp. 216225,
http://dx.doi.org/10.1111/j.1365-2451.2010.00773.x.
The earth can be considered a crystalline planet, with
thousands of ubiquitous mineral varieties occurring in
diverse geologic environments. Like larger geologic formations, these crystals are significant for deciphering Earth
history. This article discusses how specific crystals are of
geoheritage significance.
The principles of geoconservation and geoheritage as
applied to geologic sites are reviewed in detail. The article
also suggests that some crystals, because of their distinctive attributes (size, rarity, inclusions, etc.) or locality
should be afforded geoheritage status, worthy of protection through geoconservation. Eight of the 15 significant
geologic phenomena used to identify geoheritage and geoconservation significance apply to crystals and minerals.
The authors illustrate a range of internal features (e.g.,
various types of zoning and inclusions) and nine crystal
settings and features (e.g., veins, geodes, euhedrality, large
cavities, and caves). These, and other dimensions such as
arrangement of crystals (e.g., aggregations), occurrence of
unique and unusual features (e.g., largest or best formed of
its kind), and cultural value justify that crystals can be an
important basic component in a given region for understanding the larger history of the earth, and thus are significant for geoheritage and geoconservation.
An extensive table of notable crystal and mineral sites
worldwide and their significance is provided. It includes
amethyst-bearing geodes, large well-formed dravite and
elbaite tourmalines, large gypsum crystals in Mexico and
Spain, zircon crystals from Jack Hills in Australia (the oldest crystals on Earth), well-formed pyrite in Spain, and
outstanding Iceland spar (transparent calcite).
ERB
The Tucson mineral show and the market for collector
minerals: The potential for artisanal and small scale
miners. B. Ross [brad.ross@riotintocom], S. Dessureault, and M. Rieber, Resources Policy, Vol. 36,
j.resourpol.2010.11.001.
During the first two weeks of February, the city of Tucson
in Arizona hosts 43 gem and mineral shows, making it the
largest event of its kind in the world. Six of these shows
specialize primarily in collector minerals. This article
focuses on the potential for artisanal and small-scale miners to compete in the collector market. The principal challenges facing them are capital requirements and intense
competition. Because of these barriers, and the way the
shows are managed and organized, participation is difficult
or impossible for the miners. With the support of government policy makers and NGOs, alternative solutions
including the creation of a separate venue in Tucson solely
for artisanal and small-scale minersmay help these individuals find success in this lucrative market.
MK
GEMS & GEMOLOGY
FALL 2011
S13
Because Public Education

Happens At The Counter.
GIAs Retailer Support Kit and website
EPHRAIM ZION of Dehres Limited handles more

diamonds in a day than most people see in a lifetime. Here he
discusses the power of reputation, global diamond investment
and why a GIA report is vital to any business built on integrity.
A $97.00 value, shipping
and handling extra.
Whats something most people dont know about your job? Its the only business in the world conducted on trust. You
sell 1 to 5 million dollars just on the telephone, without even a signature.
A diamond dealers most valuable asset? Reputation. Yes, you need a sense of artistic value and a knack for design, but
the most essential part is integrity. You cant survive without it.
What has doing business in Hong Kong taught you about the Asian market? Its one of the strongest in the world.
GIAs Retailer Support Kit has been developed to help

sales associates educate the public about diamonds,
Every day, there are new millionaires and new businesses. Asians are very investment-conscious. Diamonds are safer and more
protable than money in a bank.
the 4Cs, and thoroughly explain a GIA grading report.
All-time favorite purchase? Most recently, a 100+ ct. D FL. Incredible brilliance and scintillation. Such a beauty. People fell
www.retailer.gia.edu
Take full advantage of all that GIA has to offer by visiting
down when they saw it.
Did it arrive with a grading report? Ha, ha. GIA, of course. What responsible businessman, with a good reputation and name,
would sell a diamond without a GIA report?
Why is a GIA evaluation so important to ones reputation? Its the most reliable, authentic, dependable gem institute in
the world. People know that, especially in the Far East. Remember what I said about reputation? A GIA report is crucial.
To order your FREE kit, log on to www.retailer.gia.edu
Business words to the wise? Selling is an idea game. The more knowledge you have, the more condence you feel.
GIA gratefully acknowledges those who, for 80 years, have used our resources to
further world expertise in gems. Invest in your success at www.gia.edu
GGWI10

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GEMS & GEMOLOGY

Diamond Stamp Collection

Because Public Education

EPHRAIM ZION of Dehres Limited handles more

GIAs Retailer Support Kit has been developed to help

the 4Cs, and thoroughly explain a GIA grading report.

Take full advantage of all that GIA has to offer by visiting

down when they saw it.

To order your FREE kit, log on to www.retailer.gia.edu

Volume 47, No. 3

Ruby and Sapphire from the Tan HuongTruc Lau Area,

NOTES & NEW TECHNIQUES

Infrared Spectroscopy of Natural vs. Synthetic Amethyst: An Update

Exploring the Origin and Nature of Luminescent Regions in

Identification of Extraterrestrial Peridot by Trace Elements

A History of Diamonds through Philately: The Frank Friedman Collection

2011 Challenge Winners

Gem News International

Book Reviews/Gemological Abstracts Online Listing

Editor and Technical Specialist

Editors, Lab Notes

Editor, Gem News

Editors, Gemological Abstracts

Editors, Book Reviews

Jan Iverson | Editor-in-Chief | jan.iverson@gia.edu

GEMS & GEMOLOGY

RUBY AND SAPPHIRE FROM THE

or more than 20 years, Vietnams Yen Bai

region (Voi, 1991). Other gem occurrences near

See end of article for About the Authors and Acknowledgments.

RUBY AND SAPPHIRE FROM NORTHERN VIETNAM

GEMS & GEMOLOGY

Khoan Thong-An Phu area

are located on the east side of the Chay River and

in 1994 (Thang, 1998). In 1996 the Vietnam National

Figure 3. DOJI Gold &

RUBY AND SAPPHIRE FROM NORTHERN VIETNAM

GEMS & GEMOLOGY

occurrences occupy the northeastern part of Yen Bai

GEOLOGY AND OCCURRENCE

Figure 4. Local miners dig for spinel and corundum

RUBY AND SAPPHIRE FROM NORTHERN VIETNAM

The Khoan ThongAn Phu and Tan HuongTruc Lau

Figure 5. The 18.8 kg Great Star Ruby, one of many

GEMS & GEMOLOGY

Phia Bioc Complex: biotite granite,

Thac Ba Formation: quartz-mica

Nui Voi Formation: biotite-sillimanitegarnet plagiogneiss, amphibole gneiss,

Figure 6. This simplified

Khoan ThongAn Phu area (old mines)

Tan HuongTruc Lau area (new mines)

Yen Bai City

Lao Cai Province southeast to Yen Bai Province. The

ShanRed River Shear Zone (Trinh et al., 1998, 1999;

RUBY AND SAPPHIRE FROM NORTHERN VIETNAM

ed with lenses of amphibolite and marble; they are

GEMS & GEMOLOGY

Figure 7. The left sample

15, and 23 along National Road 70, and also

The primary host rocks are usually deeply weathered,