Spring 2023 Gems Gemology
Spring 2023 Gems Gemology
VOLUME LIX
FEATURE ARTICLES
2 Gemological Characterization of Montana Sapphire from the Secondary
p. 20 Deposits at Rock Creek, Missouri River, and Dry Cottonwood Creek
Aaron C. Palke, Nathan D. Renfro, Jeffrey R. Hapeman, and Richard B. Berg
Examines the mining history and geological characteristics of the three secondary sapphire
deposits in the state of Montana, as well as the properties of these sapphires (unheated and
heat-treated).
46 Morphology of Colombian Emerald: Some Less Common Cases and
Their Growth and Dissolution History
Karl Schmetzer and Gérard Martayan
Evaluates the growth mechanisms of special morphological features in Colombian emerald,
including possible relationships to trapiche emeralds and samples displaying the gota de
p. 63 aceite effect.
REGULAR FEATURES
72 Lab Notes
p. 74 Purple anhydrite • Pink pyrope garnet • Libyan Desert glass bangle • Atypical bead
cultured pearls • Treated freshwater non-bead cultured pearls with antique appearance
• Heart-shaped golden South Sea cultured pearl • Gastropod shell in a shell blister • Ruby
with synthetic overgrowth • Exceptionally large synthetic rutile
Editor
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In our lead article, Dr. Aaron Palke and coauthors present their study of the gemological
characteristics of sapphire from Montana’s secondary deposits. Using Rock Creek,
Missouri River, and
Dry Cottonwood “The article also details the fascinating history of
Creek samples in a sapphire mining in these three Montana mining
variety of colors, districts, which still hold substantial resources.”
the authors provide
typical inclusion scenes and trace element chemistry fingerprints. The article also details the fascinating history of
sapphire mining in these three Montana mining districts, which still hold substantial resources.
Next, Dr. Karl Schmetzer and Gérard Martayan investigate the less common morphological and growth
phenomena of Colombian emerald samples to understand their growth and post-growth history. Based on their
observation of 15 isolated emerald crystals and seven specimens in matrix using optical methods, they offer insight
into the different patterns, with a goal of expanding the database of morphological features in Colombian emerald.
Our regular features provide informative snapshots, beginning with Lab Notes. Highlights from the section
include a rare example of the purple collector gem anhydrite, a heart-shaped golden South Sea cultured pearl
displaying natural shape and color, and the largest sample of synthetic rutile examined at GIA to date. Explore the
inner landscapes of gemstones in our Micro-World section, where you’ll see rare cloud inclusions resembling a
starry night in diamond, a macroscopic mineral inclusion cluster in a Pakistani aquamarine crystal, a three-phase
inclusion in alexandrite, and more. Diamond Reflections returns in this issue, this time exploring plastic deforma-
tion in diamond. Our Gem News International section begins with nearly 30 pages covering the 2023 Tucson gem
shows, ranging from the latest trends and market updates to noteworthy designs, followed by an opulent photo
gallery packed with finds from the shows. The GNI regular features include various pearl discoveries from around
the world and a new source of ruby from Liberia.
Finally, test your gemological knowledge of our 2022 feature articles in the annual G&G Challenge, and find out
which articles received the Dr. Edward J. Gübelin Most Valuable Article Award.
GEMOLOGICAL CHARACTERIZATION OF
MONTANA SAPPHIRE FROM THE SECONDARY
DEPOSITS AT ROCK CREEK, MISSOURI RIVER,
AND DRY COTTONWOOD CREEK
Aaron C. Palke, Nathan D. Renfro, Jeffrey R. Hapeman, and Richard B. Berg
Montana has produced large volumes of sapphire from secondary deposits for more than 150 years. While early
production was mostly for industrial use as watch and instrument bearings, modern heat treatment technology
has enabled the deposits to be worked profitably as gemstone mines, bringing more of this material to the gem
and jewelry trade than ever before. Although pale blue and pale green sapphires make up the bulk of the pro-
duction, fine Montana sapphire comes in nearly every hue, including yellow, orange, purple, and pink, along
with very rare finds of ruby. Secondary Montana sapphire shares some similarities with those from Umba and
Songea in Tanzania, but it is generally straightforward to separate them on the basis of inclusion scenes and
trace element chemistry fingerprints.
N
early 160 years ago, gold prospectors in the oxidizing and reducing environments at high tem-
American West stumbled upon one of North peratures—can be used to either create or intensify
America’s most important gemstone de- a variety of colors (e.g., Emmett and Douthit, 1993).
posits, discovering sapphire in several locations in Whether heated or with a natural, untreated color,
Montana. These were first recovered along the Mis- secondary Montana sapphire occurs in a wide range
souri River near Helena, and additional deposits were
later found at Rock Creek and Dry Cottonwood
Creek. The sapphires recovered from these secondary
deposits generally have overlapping properties and In Brief
are collectively referred to as “Montana sapphire.” • Sapphires have been produced from three secondary
[Note that these are distinct in their gemological deposits in Montana for more than 150 years.
properties from “Yogo sapphires,” which are mined • Most sapphires produced are less than 1 ct and require
from Montana’s only primary deposit, at Yogo Gulch; heat treatment to improve their color. However, large
see Renfro et al. (2017).] Surprisingly, the secondary unheated stones of several carats are available in the
deposits were not initially mined for fine jewelry- market.
grade sapphire but for gold and for industrial-grade • Montana sapphires have characteristic inclusion suites
sapphire to use as watch and instrument bearings. and chemical profiles that allow their origin to be con-
While the deposits produce many stones with ex- fidently identified.
ceptional natural color, the majority require (or at
least benefit from) carefully controlled high-temper-
ature heat treatment to enhance their color for the of sizes and colors including blue, green, yellow, or-
jewelry market. Various heating procedures—in both ange, purple, and pink (figures 1–5). With the rein-
troduction of large-scale mining 25–30 years ago and
the recent acceleration of mining activities at Mis-
See end of article for About the Authors and Acknowledgments.
GEMS & GEMOLOGY, Vol. 59, No. 1, pp. 2–45,
souri River and especially Rock Creek, fine Montana
[Link] sapphire is available in the gem and jewelry market
© 2023 Gemological Institute of America in quantities never seen before. It is also growing in
2 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 1. Top production from Rock Creek from the 2021 mining season, in rough and cut form. The rough stones
range from 10.05 to 67.15 ct and the faceted stones from 3.09 to 12.18 ct. The yellow sapphire at top center was
named the Yellowstone sapphire and is part of the Somewhere in the Rainbow collection. For the faceted stones, the
blue stone on the left and the two blue stones on the bottom are heated, while the others are unheated. Note that
one of the rough stones is missing in the faceted stone layout. Photos by Robert Weldon; courtesy of Potentate Min-
ing, LLC.
popularity with the increasing emphasis on trans- jewelry industry. Demand is also increasing as con-
parency and traceability in supply chains within the sumers become more interested in the less saturated
Figure 2. At 17.04 ct, this natural-color (unheated) Figure 3. The “Bitterroot Flower” brooch by Paula
rough sapphire crystal from Eldorado Bar on the Mis- Crevoshay contains nearly 400 Montana sapphires: 79
souri River is exceptionally large for Montana’s sec- pink (6.03 carats total), 116 yellow (7.46 carats total),
ondary deposits. Photo by Orasa Weldon; courtesy of and 202 additional fancy-color (16.26 carats total).
Pala International. Photo by Robert Weldon; courtesy of Paula Crevoshay.
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 3
stone sapphire, but most were much smaller, from
less than a carat to several carats in size. Seventy-
three Montana sapphires were included in our laser
ablation–inductively coupled plasma–mass spec-
trometry (LA-ICP-MS) trace element measure-
ments, as well as 19 sapphires from Songea,
Tanzania, and 17 from Umba, Tanzania. The Songea
and Umba sapphires were either collected directly
in the field by GIA field gemologists or donated by
Dr. Emmett.
Ultraviolet/Visible/Near-Infrared (UV-Vis-NIR)
Spectroscopy. Spectra were collected with a
PerkinElmer Lambda 950 UV-Vis spectrophotometer
(PE 950) in the 200–1000 nm range, with 1 nm spec-
tral resolution. Spectra presented were collected
from samples oriented as wafers perpendicular to the
optic axis, which allows collection only of the ordi-
Figure 4. This “Fiume” ring features a wide range of nary ray (o-ray) spectrum. Samples used in heat
colors seen in Montana sapphire. The sapphires are all treatment experiments were mounted on aluminum
heat treated, with 2.07 total carat weight. Photo cour- plates with 1 mm apertures during spectroscopy.
tesy of Raintree Jewelry. They were set in place using wax to allow the same
region of the sample to be measured before and after
heat treatment.
blue and teal and fancy-color sapphires that are com-
mon in Montana. Fortunately, these sapphires have Fourier-Transform Infrared (FTIR) Spectroscopy.
unique gemological and chemical characteristics FTIR spectra were collected using a Thermo Fisher
that allow their geographic origin to be confidently Nicolet 6700 FTIR spectrometer equipped with an
determined. XT-KBr beam splitter and a mercury-cadmium-tel-
luride (MCT) detector operating with a 4× beam con-
MATERIALS AND METHODS denser accessory. The resolution was set at 4 cm–1
with 1.928 cm–1 data spacing.
Samples. The Montana sapphires examined in this
study are from a variety of sources. The bulk of the
samples were collected in 2015 by GIA gemologists Raman Spectroscopy. Inclusions were identified,
at the Potentate mine at Rock Creek and from Cass when possible, using Raman spectroscopy with a
Thompson’s mining operation at Eldorado Bar on Renishaw inVia Raman microscope system. The
the Missouri River. Additional samples came from Raman spectra of the inclusions were excited by a
the collections of the authors and were generally Modu-Laser Stellar-REN Ar-ion laser producing
sourced directly from current operations at Rock highly polarized light at 514 nm and collected at a
Creek and Missouri River. Sapphires from the South nominal resolution of 3 cm–1 in the 2000–200 cm–1
Fork of Dry Cottonwood Creek were donated by Dr. range. In many cases, the confocal capabilities of the
John Emmett, director of Crystal Chemistry in Raman system allowed inclusions beneath the sur-
Brush Prairie, Washington, who obtained them from face to be analyzed.
the mining operations of American Gem Corpora-
tion in 1994–1995. Observations described in this LA-ICP-MS. Trace element chemistry was collected
study come primarily from the more than 800 sap- by LA-ICP-MS using a Thermo Fisher iCAP Qc ICP-
phires in the GIA Colored Stone Reference Collec- MS, coupled to an Elemental Scientific Lasers NWR
tion gathered from the sources described above. 213 laser ablation system with a frequency-quintu-
Additional sapphires were provided from the collec- pled Nd:YAG laser (213 nm wavelength with 4 ns
tion of John I. Koivula, GIA’s analytical microscopist. pulse width). Ablation was carried out with 55 μm
The largest sapphire studied was the 67.15 ct Yellow- spot sizes, with a fluence of 8–10 J/cm2 and repetition
4 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 5. Early gold prospecting led to the discovery of Montana sapphire. This gold nugget from Scratchgravel Hills
measures about 4 × 7 cm; courtesy of Bill Larson. The rough sapphires and the necklace containing rough sapphires
and a 3.5 ct lavender spinel cut by Larry Woods are courtesy of Diana Widman. Photo by Robert Weldon.
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 5
rates of 20 Hz. The isotope 27Al was used as an inter- they were mainly targeting gold, whose value was
nal standard at 529250 ppmw, and synthetic and nat- much more obvious than the shiny dense pebbles of
ural corundum reference materials were used as sapphire they sometimes found in their jigs and pans.
external standards (Stone-Sundberg et al., 2017). De- When the first sapphires were discovered in 1865 at
tection limits ranged from 0.1–0.3 ppma for magne- the Missouri River, their range of natural colors did
sium, 0.5–2.0 ppma for titanium, 0.03–0.2 ppma for not suit the gem and jewelry industry of that time—
vanadium, 0.06–1.3 ppma for chromium, 1–5 ppma that happened 30 years later, when bright blue sap-
for iron, and 0.03–0.07 ppma for gallium. Trace ele- phires were found at Yogo Gulch. However, when
ment values are reported here in parts per million on sapphires were found in abundance at Rock Creek in
an atomic basis rather than the more typical parts per 1892, another lucrative market opened up for these
million by weight unit used for trace elements in stones as watch and instrument bearings (figure 6).
many geochemical studies. Units of ppma are the In fact, mining efforts until the late 1920s were
standard used in GIA laboratories for corundum, as driven almost entirely by the search for gold and the
they allow a simpler analysis of crystal chemical use of sapphires as watch bearings. The bulk of the
properties and an understanding of the color mecha- sapphires mined in Montana had ended up being
nisms of sapphire and ruby. Conversion factors are used for industrial purposes. The availability and af-
determined by a simple formula that can be found in fordability of synthetic ruby and sapphire (grown by
table 1 of Emmett et al. (2003). the Verneuil process) in the 1920s and 1930s ended
the first great heyday of sapphire mining in Montana
Heat Treatment. Some heat treatment studies were (Berg, 2014). After some small-scale mining to sup-
carried out at the commercial heating facility operated port the war effort in the 1940s, the major operations
by Dale Siegford of the Sapphire Gallery in Philips- in this early period ended shortly after World War II.
burg, Montana. Treatments were claimed to have It was not until the introduction of advanced heat
been at 1400°C, but other details of this commercial treatment procedures that these deposits became
treatment were not disclosed. Additional heat treat- economically viable again.
ment experiments were carried out at GIA’s experi- The following sections will document each of the
mental heating facility using a Thermal Technology three secondary sapphire deposits in more detail. His-
Model 1000-3560-FP24 muffle tube furnace, similar torical information in this section comes primarily
to the system used in Emmett and Douthit (1993). from the works of Berg (2007, 2014) and Berg and
Landry (2018), which are currently the most compre-
hensive historical works on sapphire mining in these
Gemology. Standard gemological instruments were
deposits. These three publications contain original
used to measure refractive index, birefringence, spe-
historical research based on archived historical re-
cific gravity, and pleochroism. Microscopic observa-
sources and interviews with primary historical fig-
tion was performed using either a Nikon Eclipse
ures. When possible, the primary published source of
LV100 compound microscope or Nikon SMZ1500
information is cited; however, when no citation is
binocular microscope outfitted with a Nikon DS-Ri2
provided, it should be understood that the primary
camera for recording images. Differential interfer-
reference is the original historical research in Berg
ence contrast (DIC) images were taken on the LV100.
(2007), Berg (2014), or Berg and Landry (2018) for Dry
Also used were a Nikon SMZ25 stereomicroscope
Cottonwood Creek, Rock Creek, and Missouri River,
equipped with dual fiber-optic illuminators, darkfield
respectively. Additional sources of historical informa-
and brightfield illumination, polarizing filters, and a
tion are Kunz (1890), Pratt (1906), Clabaugh (1952),
Nikon DS-Ri2 camera.
Emmett and Douthit (1993), Garland (2002), Barron
and Boyd (2015), Hsu et al. (2017), and Kane (2020).
HISTORY
Like much of the American West, the history of Missouri River. The first influx of European settlers
Montana is told in the story of gold. The original into the Montana territory began in 1862 with the
prospectors who discovered the state’s sapphire de- discovery of rich gold placers in Grasshopper Creek
posits generally had little in the way of mineralogi- at the town of Bannack. With rumors of gold circu-
cal, much less gemological, knowledge. While these lating, prospectors would seek their fortune up and
prospectors did stumble upon one of the most impor- down nearly every creek and river in the territory, no
tant gem deposits in the North American continent, matter how large or small. Gold in abundance would
6 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 6. Watch bearings fashioned out of Montana sapphires in various stages of completion. The leftmost pile
contains rough sapphires ready for fabrication, and the pile second from the left contains sapphires ground to
wafers of standard thickness to be drilled out to produce bearings. The four piles to the right show finished natural
sapphire watch bearings. Photo by Robert Weldon; courtesy of the Sapphire Gallery.
be found the next year at Virginia City in Alder The earliest workings on these bars involved hor-
Gulch and, importantly, at Last Chance Gulch near izontal drifts cut through the gravel beds, which al-
Helena. lowed miners to avoid the labor of removing the
The first report of sapphire came in 1865, when several meters of overburden that typically overlie
gold prospector Ed Collins found several while work- the sapphire- and gold-bearing gravels (figure 7). Hy-
ing a gravel deposit along the Missouri River near He- draulic mining, which had been used at other gold
lena at what came to be known as Eldorado Bar. The camps, would have been more efficient. Yet here, as
stones were found not in the river itself, but in gravel in much of the American West, this advanced min-
beds sitting atop bedrock just off the banks of the river, ing technique was limited by access to water. De-
sometimes several hundred meters above water level. spite their proximity to the Missouri River, the
Over the years, similar deposits were identified along gravel beds were at a higher elevation than the river
a roughly 21 km stretch of the Missouri River, with level, so the water would have to be pumped up to
eight major gravel bars eventually worked to some ex- the gravel beds or brought in from elsewhere. The
tent. Collins was apparently unsure what to make of first major mining efforts commenced in 1868, when
the gemmy stones he found, so he sent them east to the Eldorado Ditch Company completed a ditch
Tiffany & Co. in New York and other parties overseas from Trout Creek, at a higher elevation than the
(“Eldorado Bar sapphires,” 1867). The gems were iden- Missouri River, to bring water to the upper terraces
tified as sapphire, although the discovery generated lit- of Eldorado Bar (figure 8). This allowed the gravel
tle attention (Browne, 1868, p. 50). These gravel bars beds to be worked by hydraulic mining, in which
sitting alongside the Missouri River were also rich in high-pressure jets of water were employed to wash
gold, so mining activities continued regardless. sapphire-bearing gravels into sluice boxes with riffles
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 7
Figure 7. Mining opera-
tion at Dana’s Bar. The
piles of rock are from the
trenches below. Photo
by Edgar H. Train be-
tween 1870 and 1879,
Lot 026 B3F15.03 Dana’s
Bar, Montana Historical
Society Photograph
Archives.
set up at intervals to capture sapphire and gold (figure Company as a subsidiary of the Sapphire and Ruby
9). This led to the consolidation of smaller claims on Company of Montana, Ltd. to mine Spokane Bar.
Eldorado Bar, creating larger and more efficient oper- Given the worldwide interest being generated
ations. The process of consolidation continued until about the Missouri River deposit, other mining en-
1872, when original discoverer Ed Collins joined terprises came along as well. Notably, Henry Math-
with seven partners to control a 641 hectare claim eson acquired claims on Emerald Bar and brought in
encompassing most of the upper terrace of Eldorado water with the use of a steam pump. Matheson soon
Bar. sold out to a group of investors out of Helena forming
During a lull in mining in the 1880s, brothers the Montana Gold and Gem Company.
Frank D. and Thomas H. Spratt began buying up and Despite the budding success of Missouri River
staking new mining claims, especially on Eldorado sapphires, which were featured at the 1893 Chicago
Bar. In 1887, with the financial backing of a third World’s Fair, the economic Panic of 1893 crippled the
brother, Augustus N. Spratt, they incorporated the market for them. This was compounded, in no small
Trout Creek Mining Company and began actively part, by the discovery in 1895 of sapphires at Yogo
marketing the sapphires on a national and interna- Gulch whose natural cornflower blue color was pre-
tional scale. In 1890, an English syndicate was ferred in the gem market. Shortly thereafter, the Sap-
formed to market Missouri River sapphires. The syn- phire and Ruby Company of Montana, Ltd. went
dicate ended up purchasing properties on Ruby Bar bankrupt and its properties reverted to Augustus N.
owned by Frank and Edgar Langdon, as well as prop- Spratt, who reformed his holdings as the Eldorado
erties belonging to the Spratt brothers at French Bar Gold and Gem Company.
and their Eldorado Bar claims. The English syndicate In 1911, the lowest terraces of Eldorado and
now controlled most of the profitable workings and Spokane Bars were submerged with the completion
was incorporated as the Sapphire and Ruby Company of the Hauser Dam and the creation of Hauser Lake.
of Montana, Ltd. with initial public stock offerings While it may seem a pity to flood precious gem-
of 400,000 shares at £1 (“Montana’s precious stones,” bearing gravels, the advantages of the newly created
1891; “Sapphire and Ruby Company prospectus,” lake did not go unnoticed. Most notably, in 1938, the
1891). Sapphire and gold production commenced Perry-Schroeder Mining Company was formed and
swiftly, with drift mining utilized initially and hy- purchased a Yuba bucket-line dredge. The Perry-
draulic mining techniques applied later. The Spratt Schroeder Mining Company was one of the few op-
brothers also incorporated the Spokane Sapphire erations allowed to continue mining gold throughout
8 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 8. The flume tak-
ing water from Trout
Creek to the sapphire
and gold mining opera-
tions at the Missouri
River. In this view, the
flume is crossing Trout
Creek itself, with the
water taken from further
upstream. Photo by W.H.
Jackson during the 1869–
1871 Hayden Survey. Lot
032 B5F09.03a Trout
Creek Flume, Montana
Historical Society Photo-
graph Archives.
World War II despite War Production Board Order L- strategic materials. The company was only allowed
208, which shut down gold mining operations across to continue mining gold because it was also produc-
the country in order to focus extraction efforts on ing industrial sapphire, which was in short supply
Figure 9. Hydraulic
mining at French Bar
along the Missouri
River between 1870
and 1879. PAc 97-32.9,
Montana, Montana His-
torical Society Photo-
graph Archives.
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 9
given that the synthetic sapphire manufacturers Rock Creek. The discovery of sapphire in the Rock
were all located in Europe at the time. The Yuba Creek district is often attributed to one Emil Meyer,
dredge continued mining for gold and sapphires until a German immigrant who later partnered with Swiss
1947, marking the end of the historic mining activi- native L.J. Moffat to work the deposit (“Sapphire
ties on the Missouri River. In the ensuing years, sev- mined on Rock Creek after 1892 discovery there,”
eral smaller operations continued to mine for 2019). However, some reports attribute the discovery
sapphire along the gravel bars of the Missouri River. to M.H. Bryan Sr. of Philipsburg, who claimed to
Their efforts have been fueled by the development of have been prospecting for gold on the West Fork of
high-temperature heat treatment processes to im- Rock Creek when he noticed several bright stones at
prove the sapphire colors, making them more desir- the bottom of each pan of dirt. He collected the
able in the global gem and jewelry market. Today, the stones and simply gave the choice gems to his grand-
mining is nearly all concentrated on Eldorado Bar, children to play with. Regardless of who truly dis-
where small-scale miners work some virgin gravels covered the deposit, or whether they found it more
but mostly the tailings left over from the Perry- or less contemporaneously, the recorded date of dis-
Schroeder Mining Company in the 1940s. As that covery is 1892. An article from the September 3,
dredging operation was also tailored to recover gold, 1892 edition of The Anaconda Standard (“New sap-
the company’s sapphire recovery was fairly low com- phire fields,” 1892) indicates that local prospectors
pared to modern operations, and many sapphires were already aware of the rich sapphire diggings and
were left behind. were actively preparing to start working the deposit.
Between 1988 and 1993, Sam Speerstra mined six While this deposit is colloquially referred to as
million carats of sapphire from Eldorado Bar (Berg “Rock Creek,” sapphires have largely been mined
and Landry, 2018). Adjacent to American Gem Cor- from several tributary gulches that cut into the moun-
poration’s main lease, Gem Resources Management tain to the north of the West Fork of Rock Creek. The
Corporation mined Eldorado Bar from 1988 to 1992. two most important, especially in the early days of
While American Gem Corporation’s primary mining mining, were Anaconda Gulch and Sapphire Gulch,
activities were focused at Rock Creek (see “Rock but mining has taken place at numerous gulches as
Creek” history section below), their press release well as in placers along the banks of the West Fork of
from September 1994 indicated that consulting geol- Rock Creek, in an area called the Meadow. Also of par-
ogists and engineers had completed bulk sample test- ticular note for this deposit is the relative lack of gold,
ing on 260 of the nearly 1,200 acres (105 of 485 ha) at especially compared to the Missouri River deposit.
Eldorado Bar controlled by the company (O’- What Rock Creek lacks in gold it more than makes
Donoghue, 1995). These tests were conducted to de- up for with an overwhelming abundance of sapphire.
termine occurrence and grades (carats per cubic yard) Rock Creek has produced more than any other deposit
and indicated considerable sapphire reserves at Eldo- in Montana, including Yogo Gulch, likely eclipsing all
rado Bar. American Gem Corporation also conducted of them combined by nearly a factor of 10. All told, at
test sampling across the river channel at Dana’s Bar. least 70 metric tons of sapphire have been mined from
The company never moved beyond the testing the Rock Creek area (Berg, 2014). However, this esti-
phases, electing instead to concentrate its efforts at mate does not include the mid-1990s yield of nearly 4
Rock Creek and Dry Cottonwood Creek. million carats by the American Gem Corporation or
Present-day mining includes operations of the significant recent production from Potentate Mining
Spokane Bar mine and Gold Fever Rock Shop (cur- (Kane, 2020). In fact, Rock Creek is the only secondary
rently the largest operation), Neal Hurni with Lewis deposit in Montana to be worked only for its sapphire
and Clark Sapphires, Blaze Wharton with Blaze-N- content (gold is recovered there as well but has never
Gems, Bruce Scharf and Blue Jewel mine, Don John- been the primary focus of mining).
son with Obsessed Over Gems, and Tim Beard along The early years saw the deposits worked mostly
Gruell’s Bar. Another notable operation in the recent by smaller operations. Figures of note from the first
past is that of Mac Mader, who constructed a suction few years include 400,000 carats of sapphires pro-
dredge in use from 1983 to 1986 to recover gold and duced by William Knuth of Helena and William Mof-
sapphire from Hauser Lake. In 2012, Mader used a fitt of Philipsburg in 1900, of which 25,000 carats
handheld suction dredge operated from a small barge- were fit for cutting. L.J. Moffat and Emil Meyer were
mounted washing plant on Hauser Lake near French two of the important early miners at Rock Creek.
Bar. Moffat’s Swiss heritage may have helped position
10 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 10. A 1908 map
of the mining claims of
the American Gem Syn-
dicate at Rock Creek.
The various placers are
labeled along with
water-carrying ditches
and streams. Map A-
457, Plat of the claims
of the American Gem
Mining Syndicate, Gran-
ite County, 1908, Mon-
tana Historical Society
Photograph Archives.
these stones in the industrial sapphire market, as in upper Sapphire Gulch, the Star Placer in lower Sap-
most of the production was used by fine watchmak- phire Gulch, and the Anaconda Placer in Anaconda
ers in Switzerland. Their importance in the early Gulch. The company would continue acquiring land
days of mining was recognized with the naming of and patenting placer claims through 1915 (figure 10).
sapphire-bearing gulches. Meyer Gulch was a produc- As with the Missouri River deposit, water has al-
tive tributary of Sapphire Gulch, and Moffat has two ways been the limiting factor in mining operations
gulches named in his honor: the Little Moffat and the at Rock Creek. Water flowing through the gulches
Big Moffat. was insufficient to sustain major mining activity.
The most important era of overall production at With the vast capital it raised, the American Gem
the Rock Creek deposit began in 1901, when articles Mining Syndicate solved this problem at Rock Creek
of incorporation were filed for the American Gem by constructing a series of ditches and flumes. The
Mining Syndicate, based in St. Louis. The company first was Cralle’s Ditch, likely in 1904, which
was incorporated by David Jankower of London and brought water from Stony Lake to the McLure placer
New York; Paul A. Fusz, Moses Rumsey, and Charles at the upper end of Sapphire Gulch, although the
D. McLure of St. Louis; L.S. McLure of San Diego; and water was likely used in Anaconda Gulch as well. In
William Knuth of Helena. The American Gem Min- 1912, the Upper Sapphire Ditch was completed, tak-
ing Syndicate was capitalized with $300,000, with ing water from the North Fork of the West Fork of
Jankower holding 299,996 shares and one share each Rock Creek to the head of North Fork Coal Gulch
distributed to Fusz, Rumsey, A.B. Ewing, and C. and the head of Anaconda Gulch. An additional un-
McLure (“Sapphire mined on Rock Creek after 1892 named ditch was also constructed, bringing water
discovery there,” 2019). In 1902, the American Gem from the West Fork of Rock Creek upstream 1,200 m
Mining Syndicate patented claims at the Ruby Placer to the west to Sapphire Gulch.
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 11
The water from these ditches and flumes sup- In the 1970s, the Thai gem trade developed and per-
ported mining activities during the two most produc- fected high-temperature heat treatment procedures
tive years of 1906 and 1907, which yielded 6,482.3 to dramatically improve the color and clarity of pale
kg and 6,639.9 kg of sapphire, respectively. Mining and milky sapphires, creating deep, rich blue sap-
was carried out by either ground sluicing or hydraulic phires. The original material used was the milky
mining. During these years, mining activities were geuda sapphire from Sri Lanka, but it was soon real-
intense and the mine often operated 24 hours a day. ized that the same heat treatment method could be
From 1903 to 1928, while the American Gem Mining applied to secondary Montana sapphire with out-
Syndicate was working the deposit, 46.4 metric tons standing results. In the early 1980s, a Mr. McCarthy
of sapphire were produced (Berg, 2014). of Helena was reportedly the first person in Montana
Meanwhile, times were changing with increasing to use this high-temperature heat treatment to im-
competition from synthetic ruby and sapphire, espe- prove the color of a Montana sapphire; however, the
cially starting in the 1920s. Although Auguste process was perfected in a technical sense in the
Verneuil grew his first flame-fusion rubies in 1883, 1990s and scrupulously detailed in the work of Em-
the material did not become widely available until mett and Douthit (1993).
the 1910s, when he expanded his enterprise. As more With the ability to transform color through heat
and more flame-fusion ruby and sapphire reached the treatment, the economics of mining and marketing
market, and as the quality of the laboratory-grown Montana sapphire changed for the better. In 1994, a
material improved, Montana sapphire could not new player entered the scene when American Gem
compete. Facing a dire financial situation, the Amer- Corporation purchased much of the gem-producing
ican Gem Mining Syndicate sold most of its claims areas of the Rock Creek district, including the Dann
to Charles Carpp Jr. and J. Walt Kaiser. The two Placer and Anaconda Bench as well as the holdings of
worked the deposit until 1943 and produced about the Gem Mountain Sapphire Corporation. All told,
2.8 metric tons of sapphire, largely through hydraulic American Gem Corporation reported production of
mining (Clabaugh, 1952). They apparently intended more than four million carats of gem-quality rough
to sell the sapphires as gemstones but were unsuc- sapphire, of which more than two million heat-
cessful due to the typically pale colors of the natural treated faceted sapphires to date have been sold into
rough. Therefore, most of the production still went the international market (Kane, 2020). While Ameri-
to the industrial sapphire market. can Gem Corporation, a public company listed on the
After Carpp and Kaiser stopped mining in 1943, Toronto Stock Exchange, carried out a high-profile
the Rock Creek properties passed through several marketing campaign, their efforts never materialized
hands. Carpp and Kaiser sold to Sally and Bill Eaton, into a steady supply of gems, and the company reor-
who operated a fee dig for tourists. The Eatons in ganized as an e-commerce entity in 1999. At this
1966 sold the Meadow property along the West Fork point, Chris Cooney purchased their claims at the
of Rock Creek to Marc Bielenberg and the gulch Anaconda and North Fork Coal gulches, where he
properties to Wilfred Chaussee, who formed the now operates a mining and fee-dig tourism operation
Chaussee Sapphire Corporation and continued run- called Gem Mountain. At the same time, logging
ning the tourist operation. This operation was later company RY Timber acquired the rest of the patented
passed to Wilfred’s daughter and son-in-law, Yvette claims in the Rock Creek deposit.
and Kenneth Clevish. The Clevishes sold in 1980 for The next chapter in the Rock Creek story is being
$1 million to Ted Smith, who renamed the operation written by Potentate Mining. In 2011, Potentate pur-
the Gem Mountain Sapphire Corporation. In the chased Eureka Gulch on the north side of the moun-
meantime, Marc Bielenberg sold the Meadow prop- tain and became the largest landholder on Gem
erty in 1978 to Skalkaho Grazing, Inc., which con- Mountain in 2014 after purchasing most of the south
structed a floating wash plant in 1982 near the side of the mountain from RY Timber. Over the
confluence of the Anaconda and Coal gulches with years, Potentate has actively developed its claims and
the West Fork of Rock Creek. now operates a modern operation utilizing state-of-
Still, mining activities during this period never the-art mining technologies to produce sapphire in
approached the production by the American Gem an environmentally friendly manner while making
Mining Syndicate in the early twentieth century. efficient use of limited water resources. Among the
However, another technological advance on the hori- advances implemented are a new gravel-processing
zon would change the fate of Rock Creek sapphire. facility with a separate gold circuit to maximize gold
12 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
recovery, as well as a water clarifier to ensure the re- wood Creek (Kane, 2020). However, the Dry Cotton-
turn of clean water to the pristine mountain streams. wood Creek sapphires did not react as well to heat
In 2020, Potentate finalized the purchase of the treatment as those from Rock Creek (J.L. Emmett,
Meadow property and now controls the bulk of the pers. comm., 2022), and American Gem Corporation
sapphire-bearing areas of the Rock Creek deposit. Po- abandoned operations there in 1996 to focus on Rock
tentate is pursuing an aggressive marketing cam- Creek. In the same year, Gem River Corporation
paign to put Montana sapphire in a prominent place began mining sapphires in the Grand Pre Flats, but
in the world market. mining stopped in 1998 and the area was reclaimed
for nature. No serious mining efforts have taken
Dry Cottonwood Creek. Sapphires were first found place at Dry Cottonwood Creek since then. How-
by gold prospectors in the South Fork of Dry Cotton- ever, the Dry Cottonwood Creek sapphires do react
wood Creek near the city of Butte in 1889 (Kunz, well to heat treatment in an oxidizing environment
1894). Mining commenced shortly thereafter by the to produce variegated yellow and orange colors (R.E.
Northwest Sapphire Company of Butte, which em- Kane, pers. comm., 2022). With changing market be-
ployed hydraulic mining as well as dredging opera- havior and growing interest in such fancy-color sap-
tions at the South Fork of Dry Cottonwood Creek phires, Dry Cottonwood Creek has the potential to
(Struthers and Fisher, 1903). One of the more signif- become a viable mining property.
icant mining enterprises involved the Variegated Sap-
phire Company, which in 1905 installed a
bucket-line dredge at the Grand Pre Flats, an open CHARACTERISTICS OF THE DEPOSITS
area along the South Fork of Dry Cottonwood Creek. Geology. The rugged terrain and landscapes of west-
The dredge worked an area 24–30 m wide, removing ern Montana are the product of both ancient and
12 m of gravel per day and recovering both gold and modern geological forces at work. The very oldest
sapphire. In 1907, ownership of the enterprise trans- rocks encountered in the sapphire-producing areas be-
ferred to Mr. West Dodd of Des Moines, but this op- long to the Proterozoic Belt supergroup, which forms
eration ended by 1911, only to be briefly revived in the bedrock underlying much of the Missouri River
1914 by Nat Simon. However, Simon abandoned it and Rock Creek deposits and also represents much of
after one season of low gold yield and sapphires that the Belt Mountains seen to the east of the Missouri
were pale and not marketable. In 1908, the Consoli- River deposits. The Belt supergroup includes
dated Gold and Sapphire Mining Company of Butte metasedimentary rocks deposited between 1470 to
installed another dredging operation about 1.5 km 1370 Ma in a sedimentary basin formed at the margin
from the Grand Pre Flats, downstream from the of the North American Craton and some other un-
South Fork of Dry Cottonwood Creek. This effort known ancient landmass. The Belt supergroup, an ac-
was short-lived as well due to the low concentration cumulation of sediments an astonishing 15 km thick
of gold and the difficulty of selling the sapphires in at its maximum extent, provides many clues to the
the gem and jewelry industry. ancient movement of the earth’s protocontinents. But
Interest in the Dry Cottonwood Creek deposit re- these primeval geological formations serve as nothing
vived during World War II due to the shortage of in- more than the backdrop of the gemological story. At
dustrial laboratory-grown sapphire coming from the Missouri River, these ancient formations are sim-
Europe, but there was no production in those years. ply the bedrock upon which the sapphire-bearing
Significant mining did not resume until the 1990s, gravels were deposited. The Proterozoic Belt super-
when American Gem Corporation acquired claims group formation here is in the form of an argillite, a
here and at Rock Creek and Missouri River. Ameri- low-grade metamorphosed version of a sedimentary
can Gem Corporation purchased land in 1993 from shale or claystone. At Rock Creek, the Belt super-
Scott Wurster, who had in turn acquired it from Marc group rocks include metasedimentary rocks that un-
Bielenberg, who had previously owned claims in the derlie Cenozoic volcanic formations, which are
Rock Creek district. The advent of high-temperature apparently related to the gem deposits.
heat treatment made Montana sapphire much more The story of sapphire formation begins much later
attractive to the gem and jewelry industry with the in the earth’s history, during the Cenozoic era. While
rich vivid blue and fancy-color gems that could be the sapphires occur in secondary deposits, field ob-
produced. In 1995, American Gem Corporation servations indicate in each case that the original host
mined 400,000 carats of sapphire from Dry Cotton- rock is most likely related to Cenozoic volcanic for-
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 13
MONTANA
N
S m it
UPPER
HOLTER
h R iv
LAKE
American Bar
er
Hauser Dam
Figure 11. Map of sap-
H AU
phire-bearing gravel
Eldorado Bar
bars along the banks of
SER
H E L E N A VA L L E Y
R E G U L AT I N G R E SE RVO I R
Emerald Bar
C A N YON
FER RY
LAKE
mations erupted around 50 Ma. From about 160 to 11). The sapphire-bearing gravel beds are composed
50 Ma, the entire western seaboard of North America predominantly of locally sourced material. This
was a convergent margin, with the ancient Farallon means there are limited options to consider for poten-
plate being subducted beneath the North American tial bedrock sources of the sapphire. Further compli-
continent. Subduction of the Farallon plate led to sig- cating matters is that the Missouri River here has
nificant volcanism throughout the western United been flooded by the construction of the Hauser Dam
States, Canada, and Mexico. The volcanic formations and subsequent creation of Hauser Lake, limiting po-
in the region of the sapphire deposits are related to tential exposures of sapphire-bearing lithologies. The
the late stages of this period, when a flat-lying Faral- Proterozoic Belt supergroup argilites immediately un-
lon slab started to roll back and eventually detach as derlying the gravel beds are not suitable lithologies
it continued its descent into the earth’s mantle. As for corundum formation, and the same is true for the
the sapphire-bearing volcanic formations were Paleozoic and Proterozoic metasedimentary rocks of
weathered and broken down, the sapphires were lib- the nearby Big Belt Mountains and the Paleozoic sed-
erated and entrained in the rich gem gravels being imentary rocks in the Spokane Hills.
mined to this day. The following sections will briefly What little evidence we have comes from one
describe the relevant formations in each deposit. small sapphire-bearing sill found at French Bar.1
14 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Based on chemical analysis and petrographic obser- tirely. Additionally, many sapphires from the Mis-
vations of thin sections of the volcanic rock, Berg and souri River are found with thin encrustations of
Palke (2016) described it as a basaltic trachyandesite spinel adhering to their surface. This spinel is in-
composed of biotite and augite phenocrysts in a ma- ferred to result from a reaction between the corun-
trix of plagioclase microlites. Rare corundum-bearing dum and magnesium and iron sourced from mafic
xenoliths have been found composed of calcic plagio- magmas that transported the sapphires to the sur-
clase, augite, garnet, margarite, and spinel (Berg and face. This spinel rim is not found on sapphires from
Dahy, 2002). Rock Creek or Dry Cottonwood Creek and is not
Importantly, Berg and Palke (2016) used LA-ICP- even found on all Missouri River sapphires.
MS to analyze the chemistry of sapphires found in
situ in this (sub)volcanic formation, and the results Rock Creek Geology. In the Rock Creek area, sap-
demonstrated that their trace element profiles are phires are found in gravel beds in gulches cutting into
consistent with the gem sapphires found in the Gem Mountain (figure 12). The dominant formations
gravel beds. This indicates that these volcanic forma- in the area are rhyolitic lava flows, dikes, and tuffa-
tions are viable sources of the Missouri River sap- ceous and volcaniclastic formations that overlie
phires. While this single volcanic formation is surely metasedimentary rocks of the Proterozoic Belt super-
too small and has too low a sapphire concentration group. Given that sapphires are found in the gulches
to have supplied gems for the entire Missouri River cutting up into the mountain, their source must have
deposit, it suggests a likely geological origin of the been local. The volcanic formations here are rela-
sapphires, with the implication that other similar tively silica-rich and rhyolitic in composition. Rhy-
sapphire-bearing (sub)volcanic formations must have olite lava flows cap the ridges separating the
been present but were weathered away almost en- sapphire-rich gulches, while the more readily eroded
N N
O
R
T
H
Coal
SA
Gulch PP
HI
Pit RE Ewing
Placer
Dismal
F O R K
Swamp C
H
McLure L
U
Anaconda Placer G
Wild Cat Gulch A
Bench O
R
A NA
R
ulch
U
A
kG Meyer Gulch
Min lch
C O N
e Gu
Pin Queen Gulch
ck
DA
Bla
H
ch
G U L C
G U L C H
Figure 12. Map of sap-
Gul
C OA L
L
G
GU
phire-bearing gulches
U
May
Y
L
C
AT
H
GU
Bench
H
Placer
LC
Placer
L I T T
The Meadow
Sapphire
MONTANA Gulch
S m it
h R iv
er
Big Moffat
Gulch
Sapphire-bearing gulches
and placers
Qal (quaternary alluvium) 0 1 km
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 15
tuffs and volcaniclastic units are less well preserved. Origin of the Secondary Montana Sapphires. Given
No other volcanic formations have been identified in the relative lack of hard rock geological evidence in
the immediate area, although it has been postulated these secondary deposits, one must search elsewhere
that there may be hidden plugs of lamprophyres or for clues about the ultimate origin of these sapphires.
other mafic volcanics in the area that have supplied In fact, while the original sapphire-bearing host rocks
the sapphires (Barron and Boyd, 2015). Notably, Berg have mostly weathered away, remnants of the an-
(2014) did identify a basaltic dike exposed along a cient sapphire-producing geological environments
road cut 4 km east of Sapphire Gulch. No sapphires have been preserved within the sapphires as inclu-
have been found in this dike, but to the authors’ sions. Besides hexagonal bands of silk and rutile par-
knowledge it has never been studied thoroughly. ticles, among the most commonly encountered
Still, this basaltic dike is likely too small and too far inclusions are fluid inclusions of an unusual nature.
from the deposit to be a viable source of the sap- These often have the appearance of typical two-phase
phires. While no sapphires have been found in situ fluid inclusions seen in other gems. However, if one
in any volcanic rocks here, Berg (2014) did identify were to cut into one of these fluid inclusions, the
some with what was described as a “rhyolitic” en- fluid material would be frozen in place and not leak
crustation. This encrustation was observed on an- out of the sapphire as expected. These fluid inclu-
other sapphire by Belley (2022), with scanning sions represent blebs of magma and indicate that the
electron microscopy (SEM) images confirming that fluid present during sapphire growth was a molten
the adhering crust was composed of quartz, plagio- silicate rock. Upon transport to the surface in vol-
clase, and potassium feldspar. Importantly, Rock canic events, the sapphires must have cooled quickly
Creek sapphires are never found with the spinel en- enough to quench these melts into glasses.
crustation found on some Missouri River sapphires, The compositions of the melt inclusions are
which is likely formed by interaction with magne- broadly similar across the three deposits, suggesting
sium and iron in the mafic transporting magma at similar conditions of geological formation. The melts
Missouri River. This observation seems to suggest a coexisting during sapphire growth were poor in MgO
mafic source is less likely at Rock Creek. With the and FeO, moderately enriched in Na2O, K2O, and
enormous volume of sapphire produced at Rock CaO, and (surprisingly) relatively rich in SiO2. The
Creek, the original source rock must have been ex- melts can be classified as dacites or rhyolites accord-
tensive, decreasing the likelihood of a hidden source ing to the total alkali silica (TAS) diagram of Le Bas
that was weathered away. Given the prevalence of et al. (1986). Of particular note is that these melts are
rhyolitic volcanics in the area, the evidence suggests all quartz-normative, meaning that if cooled in an
that rhyolitic volcanism is a likely source of the sap- isolated system, they should have precipitated
phires in this deposit. quartz. This seems counterintuitive at first, as it is
well known that corundum and quartz cannot coex-
Dry Cottonwood Creek Geology. Sapphires at Dry ist under ordinary geological conditions. However,
Cottonwood Creek are found in gravels and second- it is possible for corundum to coexist with a quartz-
ary deposits. Bedrock is composed of volcanic for- normative melt in the case of an incongruent (or
mations from the Eocene-age Lowland Creek peritectic) melting reaction. The presence of quartz-
Volcanics. These overlie Cretaceous granitic rocks normative melts then suggests a genetic model in
of the Boulder Batholith, which contacts the Low- which the secondary Montana sapphires grew
land Creek Volcanics near the western boundary of through partial melting of some aluminum-rich rock
the Grand Pre Flats on the South Fork of Dry Cot- (e.g., an anorthosite or some similar plagioclase-rich
tonwood Creek. The Lowland Creek Volcanics are igneous rock). In this model, the magmas that trans-
predominantly composed of welded tuffs and lava ported the sapphires to the surface in volcanic
flows of dacitic composition. No other volcanics or events might have also been responsible for sapphire
other geological formations exist in the immediate formation by initiating partial melting of the pro-
area. While no thorough field studies have been per- posed aluminum-rich protoliths. In this scenario,
formed to identify the source of the sapphires, the the sapphires could still be foreign to the transport-
Lowland Creek Volcanics seem to be a likely origi- ing magmas but would not be accidental xenocrysts.
nal bedrock source, given the likely volcanic origin In fact, based on observations of rhyolitic secondary
of all Montana sapphire and the paucity of other pos- melt inclusions, Palke et al. (2017) suggested the
sible sources. possibility that some sapphires at Rock Creek may
16 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
not be xenocrysts at all if the partial melting event
that produced the rhyolites seen at the surface also
produced the sapphires entrained in this magma. Of
course, proving or disproving this hypothesis would
be challenging. At Missouri River, the basaltic tra-
chyandesite magma that likely transported some of
the sapphires is significantly different from the melt
inclusions seen in those stones, confirming their
identity as xenocrysts. The Lowland Creek Volcanics
at Dry Cottonwood Creek have not been thoroughly
studied, and their relation to the melt inclusions seen
in those sapphires is less clear.
The sapphires’ origin from some calcium- and
aluminum-rich protolith such as an anorthosite is
also supported by the prevalence of calcium- and
aluminum-rich mineral inclusions such as anor-
thite-rich feldspar and (clino)zoisite. Other genetic
models have been proposed, mostly based on the use
of trace element chemistry wherein the low gallium
and other trace element patterns were thought to
suggest a metasomatic or metamorphic origin for
the sapphires (Garland, 1992; Zwaan et al., 2015).
Such an origin, however, seems to be contradicted
by the pervasiveness of silicate melt inclusions,
which indicate that the sapphires grew in the pres-
ence of a silicate magma.
Figure 13. Faceted unheated Montana sapphires set in
18K gold. Photo by Orasa Weldon; courtesy of Diana
Widman.
GEMOLOGICAL CHARACTERISTICS OF
SECONDARY MONTANA SAPPHIRE
Physical Properties. Sapphires from Montana’s sec- observed, especially for heated stones with a yellow
ondary deposits yield some unique characteristics or orange core and a blue, green, pink, or violet rim
that make them distinct from other sapphires around
the world. While basic physical properties such as re-
fractive index and specific gravity offer no significant Figure 14. This “Twilight” ring showcases some of the
differences, the inclusion suite and trace element common range of colors seen in Montana sapphire.
chemistry can help to distinguish secondary Mon- The sapphires are unheated, with 3.80 total carat
tana sapphire. However, it should be noted that the weight. Photo courtesy of Earth’s Treasury.
characteristics of individual faceted sapphires from
Montana’s secondary deposits overlap significantly,
and these gems cannot currently be reliably sepa-
rated from each other.
In general, sapphires from Montana’s secondary
sources naturally occur in a wide range of hues, in-
cluding blue, green, yellow, orange, pink, and purple
(figures 13–19). Most of these colors are somewhat
pale, especially when unheated (figures 13 and 14).
Vibrant, saturated colors do occasionally occur nat-
urally, but they are more common in heated stones
(figures 15–17). Montana sapphire has become in-
creasingly popular in nonstandard cutting styles (fig-
ures 18–19). Parti-colored sapphires are frequently
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 17
Figure 15. The “Conchita
Sapphire Butterfly,” a
collaboration between
gem dealer/gemologist
Robert Kane and jew-
elry designer Paula
Crevoshay, highlights
the variety and color
range of heat-treated
secondary sapphires
from Montana. The 18K
yellow gold butterfly is
set with 331 round bril-
liant sapphires and two
cabochon-cut sapphires,
totaling 27.97 carats.
The butterfly was do-
nated by Kane and
Crevoshay to the Smith-
sonian Institution’s Na-
tional Gem Collection
in 2007. Photo by
Harold and Erica Van
Pelt; courtesy of Robert
E. Kane.
(figure 20). Some sapphires exhibit a weak to mod- Robert Kane (Fine Gems International, Helena) un-
erate color change when observed in incandescent covered numerous examples of rubies from color-
to daylight illumination (figure 21). Colors generally graded parcels of pink sapphire. While rare, these
change from shades of pink or orange (incandescent) Montana rubies do exist and may be encountered in
to green or violet (daylight). Rubies are also some- the market. Other examples of Montana ruby are
times found (figure 22). Palke and Hapeman (2019) known, including one particularly large faceted gem
reported only 29 g of rough ruby crystals recovered weighing 1.70 ct (Malaquias, 2018).
from more than 400 kg of mine production at Poten- Sapphire rough from these deposits generally occurs
tate’s operation at Rock Creek. While truly red gem as small crystals measuring a few millimeters in diam-
corundum from Montana’s secondary sapphire de- eter, but larger stones have been found. Notably, the
posits are rare, examination of the collection of unheated blue sapphire known as the “Big Sky” sap-
Figure 16. A suite of heated Montana sapphires, 0.76–1.04 ct, displaying a range of colors. Courtesy of Rachel Hill,
Americut Gems.
18 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 17. Various colors
of heated Missouri River
sapphire, ranging from
0.16 to 1.65 ct. Photo by
Tino Hammid; courtesy
of Fine Gems Interna-
tional and American
Sapphire Company, ©
Robert E. Kane.
phire, which sold in 2015 for $394,000, weighed 12.54 also recovered a large crystal from Rock Creek in 2018
ct (Kane, 2020). Rough crystals as large as 37.78 ct have weighing 64.14 ct, known as the “Ponderosa” sapphire,
been reported from Eldorado Bar (Berg and Landry, as well as a 67.15 ct yellow sapphire recovered in 2021
2018), while the Rock Creek deposit has produced that cut a 12.18 ct stone called the Yellowstone sap-
stones as large as the faceted 12.62 ct heated stone re- phire. This is currently part of the Somewhere in the
covered by Potentate Mining known as the “Montana Rainbow collection (again, see figure 1). Rock Creek
Queen” (@potentatemining, May 27, 2019). Potentate also produced a notable 39.14 ct stone in 2008 that was
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 19
Figure 18. With their
nonstandard colors,
Montana sapphires
have become popular
for cutters experiment-
ing with nontraditional
cutting techniques.
This 4.17 ct unheated
sapphire cut by Nadine
Marshall was sourced
from the Missouri
River. Courtesy of Ob-
sessed Over Gems.
recovered from the Anaconda Bench at Gem Mountain finest and largest sapphires produced by Potentate dur-
(Berg, 2014). The largest crystal reported from Dry Cot- ing the 2021 mining season in their rough and polished
tonwood Creek weighed 22 ct but had a flat shape and states.
therefore a low yield when cut into a gem (Berg, 2007).
While small stones under a carat are the main produc- Optical Measurements and Specific Gravity. Stan-
tion from Rock Creek, figure 1 shows a suite of the dard gemological testing of Montana sapphire reveals
Figure 19. Montana sapphires in a range of shapes and colors. All are heated, and the faceted stones range from about
0.20 ct for the 3 × 5 mm kite shapes on the left to 2.11 ct for the hexagon on the right. Photo by Dillon Sprague; cour-
tesy of Columbia Gem House.
20 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 20. Parti-colored sapphires are occasionally Figure 22. A suite of nine unheated rubies from the
found in Montana and can combine a wide range of Rock Creek deposit ranging from 0.17 to 0.58 ct.
colors. These examples, ranging from 1.62 to 3.20 ct, Photo by Kevin Schumacher; courtesy of Jeffrey R.
are all heated. Photo by Jeffrey R. Hapeman. Hapeman, Earth’s Treasury, Inc.
properties one would expect for corundum. The av- sorption bands centered around 3000 cm–1 that is
erage refractive index measured is 1.760–1.770, and often referred to as the “Punsiri peaks” but will be re-
the birefringence typically ranges from 0.008 to ferred to here as the acceptor-dominated 3000 cm–1
0.010. The specific gravity ranges from 3.98 to 4.01, series, given that these peaks are related to hydrogen
also consistent with corundum. associated with acceptor ions, in this case Mg2+, in
FTIR spectra of Montana sapphire can show a va- the corundum (Fukatsu et al., 2003; Sangsawong et
riety of features (figure 23). Commonly seen is a weak al., 2016). The acceptor-dominated 3000 cm–1 series
single peak at 3309 cm–1. This peak is believed to be is not an indicator of heat treatment for Montana
related to hydrogen in the corundum structure asso- sapphire, as these peaks sometimes occur naturally.
ciated with titanium substituting for aluminum In fact, this series of peaks is very common in un-
(Moon and Phillips, 1991). Also common in secondary heated Rock Creek sapphire but only occasionally
Montana sapphire is a peak at about 3220 cm–1. A sim- found in Dry Cottonwood Creek sapphire and almost
ilar peak is often seen in Yogo sapphire as well (Renfro never in Missouri River sapphire. The commercial
et al., 2018), but its origin is unknown. Finally, many importance of this finding will be discussed later in
Montana sapphires show the collection of broad ab- the section dealing with heat treatment. The peak at
Figure 21. Some secondary Montana sapphires exhibit a color change between incandescent illumination (left) and
daylight (right). These examples are unheated and range from 0.74 to 0.83 ct. Photos by Robert Weldon; courtesy
of Jeffrey R. Hapeman, Earth’s Treasury, Inc.
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 21
FTIR SPECTRA
0.16 0.40 0.40
A B C
ABSORPTION COEFFICIENT (cm–1)
0 0 0
3400 3200 3000 3400 3200 3000 3500 3000 2500
WAVENUMBER (cm ) –1
WAVENUMBER (cm )
–1
WAVENUMBER (cm )
–1
Figure 23. Representative FTIR spectra showing expected features for Montana sapphire, including a single
3309 cm–1 peak (A), a 3220 cm–1 peak (B), and the acceptor-dominated 3000 cm–1 series (known as the “Punsiri
peaks,” C).
3220 cm–1 can be used as an indicator of a secondary less commonly as hexagonal prisms. The rough stones
Montana or primary Yogo origin, but the other FTIR also tend to show a rounded appearance, which might
features such as the 3309 cm–1 peak and the accep- cause one to suspect they have been subjected to
tor-dominated 3000 cm–1 series of peaks are observed rounding by abrasion from water transport. However,
in sapphires from many other origins. Montana sap- close examination with a microscope often reveals
phire from all the secondary deposits may also show pronounced geometric patterns on the surface with ei-
mineral inclusion peaks in their FTIR spectra, espe- ther the hillocky-type texture seen at Rock Creek or
cially for kaolinite or gibbsite. dissolution-type etch features (figures 24–26). In fact,
the sapphire morphology from the three deposits gen-
Shape of Rough Crystals/Morphology. The sapphire erally differs enough to allow identification of the ori-
from Montana’s secondary deposits is generally tabu- gin of parcels of rough sapphires, even if individual
lar or blocky in shape and can also appear somewhat stones cannot be traced back to their source. For in-
Figure 24. SEM image showing the surface of a Rock Figure 25. Hillocky structure on the surface of a rough
Creek sapphire. The hillocks on the surface are typi- sapphire from Rock Creek shown with differential in-
cal of Rock Creek sapphire. Image by Richard Berg terference contrast imaging. Photomicrograph by
(modified from Berg, 2022). Aaron Palke; field of view 2.88 mm.
2 mm
22 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 26. Differential interference contrast imaging of the surface of a rough sapphire from Dry Cottonwood
Creek showing etch features on the basal pinacoid surface (left, perpendicular to the c-axis) and on the prismatic
crystal face (right, parallel to the c-axis). Photomicrographs by Aaron Palke; field of view 0.72 mm.
stance, some 25% of sapphires from Missouri River Figure 30 shows typical shapes for the crystals
have an incomplete or spotty dark green coating of found at all three locations. The two most com-
spinel in depressions on the surface, as seen in the monly encountered shapes are hexagonal prismatic
SEM image in figure 27. This feature is not seen in crystals with slightly developed rhombohedral faces
sapphire from Rock Creek or Dry Cottonwood Creek. (figure 30, A and B). Many show development of the
Dry Cottonwood Creek sapphire shows etching along hexagonal bipyramidal faces as well (figure 30, A and
twinning planes as seen in figure 28, which is less C). Crystals typically exhibit six-fold or three-fold
common in Rock Creek and Missouri River sapphire. symmetry on the basal pinacoid; figure 30B shows a
Finally, Rock Creek sapphire often has growth classic raised trigonal pyramid on the basal pinacoid.
hillocks on the basal surface, some with flat surfaces There are slight variations between the three de-
resembling miniature mesas (figure 24). Examples of posits in the prevalence of the various crystal shapes.
rough from each deposit are shown in figure 29. For example, the majority of the crystals from Dry
Spinel
300 μm 2 mm
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 23
A B C
Figure 29. Photos of representative lots of unheated rough from each of Montana’s secondary sapphire deposits:
Rock Creek (A), Missouri River (B), and Dry Cottonwood Creek (C). The ruler in each photo is in millimeter scale.
Photos by John Emmett.
Cottonwood Creek are tabular hexagonal crystals and can reveal the structure even in heavily etched
(figure 30C), while elongated hexagonal prisms (fig- crystals. Despite this variation at each locality, crys-
ure 30D) are particularly common at Missouri River. tals of all of these shapes can be found at any of the
At Rock Creek, most of the crystals have been so deposits.
heavily etched/resorbed that most of their crystal
faces are obscured, although color zoning and the pat- Microscopic Features. Secondary sapphires from Mon-
terns of rutile inclusions follow these crystal faces tana contain a wide array of inclusions, and these are
a powerful tool in confirming a Montana origin. In
natural, unheated Montana sapphire, the most com-
Figure 30. Typical shapes seen in rough Montana sap-
mon features are bands of rutile silk, often arranged in
phires. Crystal forms include pinacoidal faces (pc),
hexagonal patterns, either as dense hexagonal clouds
prismatic faces (p), rhombohedral faces (r), and py-
ramidal faces (py). Most common shapes are pris- (figure 31, A and B) or in a loosely packed but overall
matic crystals modified by pyramidal and/or hexagonal pattern (figure 31, C and D). The individual
rhombohedral faces (A and B); flattened, tabular particles making up the clouds may be relatively long,
hexagonal crystals terminated by rhombohedral, py-
ramidal, and pinacoidal faces (C); and elongate pris-
matic crystals (D). Figure 31 (opposite page). Typical inclusion scenes in un-
heated (A–F) and heated (G and H) secondary Montana
sapphires. A: Dense, hexagonal particulate clouds in a
A pc
B Missouri River sapphire. B: Hexagonal particulate clouds
py made up of small to medium-sized rutile needles in an
py
r pc unheated orange sapphire from Rock Creek. C: More
r loosely packed hexagonally arranged silk in an unheated
p p p p sapphire from Rock Creek. D: Fiber-optic illumination re-
p p
veals interference colors from flattened silk particles in
r
this Rock Creek sapphire. E: The rare rubies occasionally
r
py found in Montana have essentially the same inclusions
as the sapphires, such as the flattened rutile silk in this
Rock Creek ruby. F: The flattened platelet-like silk in
sapphires from Missouri River often has unusual mor-
C D pc
phology, with an atoll-like inclusion at the head of a
r
platelet particle. G: Blue color zones leaking out of proto-
pc genetic rutile inclusions in a heat-treated sapphire from
p py Rock Creek. H: Patchy blue color zoning in a Dry Cot-
r p p p p
py
p tonwood Creek sapphire, caused by dissolution of bands
r
of rutile silk into the corundum lattice. Photomicro-
graphs by Nathan Renfro (A, G, H) and Aaron Palke (B–
r F); fields of view 3.31 mm (A), 4.79 mm (B), 4.79 mm (C),
4.57 mm (D), 1.26 mm (E), 1.26 mm (F), 2.19 mm (G),
and 3.31 mm (H).
24 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
A B
C D
E F
G H
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 25
slender needles varying in size all the way to very fractures or cleavages perpendicular to the direction
short, stubby, or dusty particles. In some cases, the of elongation. Sapphires from Dry Cottonwood Creek
particles take on a flattened, platelet-like shape and are also more likely to contain zircon inclusions, es-
are highly reflective, often showing iridescent inter- pecially in clusters and galaxies of crystals resembling
ference colors with the use of an intense fiber-optic rice grains (figure 32F). Zircon inclusions are rare in
light due to a thin-film effect (figure 31, D–F). sapphire from Rock Creek and Missouri River.
Given that the majority of Montana sapphires on Mica inclusions may be seen and range from
the market have been heat treated to enhance their nearly colorless to pale shades of yellow to occasional
colors, attention must be paid to the inclusions that dark orange hues (figure 33A). Colorless rounded
can help the gemologist confidently identify this treat- feldspar inclusions are fairly common as well from
ment. The most obvious effect of heat treatment on all three deposits. Note that a number of other min-
Montana sapphire is internal diffusion of blue col- eral inclusions were documented by Zwaan et al.
oration from rutile inclusions and silk. This can be (2015) and compiled in a table of occurrence. While
seen as patchy blue color zones that precisely match many of the sapphires they studied appear to have
the original patterns of the rutile silk. This is most been heated, Zwaan et al. (2015) report a more exten-
easily observed using diffuse transmitted illumina- sive list of minerals identified in their study and from
tion, but fiber-optic illumination can be useful as well. other literature sources as well.
This will lead to patchy blue color zoning surrounding In some rare sapphires from Missouri River, un-
bands of silk that are partially or nearly completely usual multiphase inclusions have a negative crystal
dissolved into the corundum lattice (figure 31G) as morphology in which the shape of the inclusion is
well as dark, inky spots surrounding protogenetic ru- constrained by the crystal forms of the corundum
tile inclusions (figure 31H). More examples will be host and not by the minerals inside the inclusion.
shown in the section on heat treatment below. These multiphase inclusions are composed of mica,
On rare occasions, rutile silk may be dense enough spinel, and some other unidentified phases (figure
to produce a star sapphire when cut in cabochon form 33B). These inclusions are interpreted to have been
(figure 32A). Yet star sapphires from Montana are ex- entrapped initially as a melt phase, which recrystal-
ceedingly rare, and the star is usually poorly devel- lized post-entrapment. In fact, melt inclusions with
oped. Many of them show interesting coloration, with a negative crystal shape are quite common in second-
yellow or orange zones in the core of the crystal, ary Montana sapphire. They often are surrounded by
which is most prominent in heat-treated stones (figure decrepitation halos, which may be partially healed
32B). Twinning with tube-like structures at the inter- and show iridescent interference colors (figure 33C).
section of twin planes is fairly common in sapphires In many cases, these inclusions look like standard
from Dry Cottonwood Creek but may occasionally be two-phase fluid inclusions (figure 33, D and E). How-
seen in sapphires from Rock Creek and Missouri ever, when one of these inclusions is cut into at the
River. These features are observed in sapphires from surface of a stone, the apparently fluid phase does not
other deposits as well (Hughes, 2017) and have been flow away but is frozen in place (figure 33F). These
referred to as “Rose channels” (Notari et al., 2018). inclusions were trapped as a relatively silica-rich
(Note that Rose channels have been referred to erro- melt (Palke et al., 2017) that coexisted with the sap-
neously in the past as “boehmite needles.”) Large, phires as they were growing. After being emplaced at
blocky protogenetic rutile inclusions are common in the earth’s surface, the sapphires must have cooled
stones from all the Montana secondary deposits (figure quickly enough to quench the melt phase into a
32C). In this study, garnets were occasionally encoun- glass. Note that while these inclusions resemble the
tered in sapphires from Dry Cottonwood Creek (figure “melted crystal” inclusions seen in heat-treated sap-
32D). Although Zwaan et al. (2015) observed garnet phires, it is not correct to apply this term to these in-
inclusions in sapphire from Rock Creek and Missouri clusions. These are properly called “melt
River, the present authors have not; these inclusions inclusions,” as they were included as a melt and do
are likely rare compared to material from Dry Cotton- not represent crystalline inclusions melted by artifi-
wood Creek. Garnet inclusions could then be consid- cial heat treatment. Therefore, observation of this
ered a likely indicator of Dry Cottonwood Creek type of inclusion is not, in and of itself, evidence of
origin. Sapphires from all three deposits are likely to heat treatment in Montana sapphire. Identification
contain inclusions of clinozoisite, which takes on an of heat treatment is more reliably carried out by ob-
elongate form (figure 32E), sometimes with multiple servation of the altered crystalline inclusions, the al-
26 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
A B
C D
E F
Figure 32. A: Dense rutile silk in a star sapphire from Rock Creek. B: Yellow core in a heated sapphire from Mis-
souri River. C: Protogenetic rutile inclusion in a Rock Creek sapphire. D: Garnet inclusion in a sapphire from Dry
Cottonwood Creek. E: Clinozoisite inclusion in a Dry Cottonwood Creek sapphire. F: Field of zircon inclusions in
a sapphire from Dry Cottonwood Creek. Photomicrographs by Nathan Renfro (A–E) and Aaron Palke (F); fields of
view 2.56 mm (A), 6.26 mm (B), 1.30 mm (C), 2.82 mm (D), 2.09 mm (E), and 1.26 mm (F).
tered nature of rutile silk particles, and/or color dif- highly lustrous surface with the use of a fiber-optic
fusion around rutile or silk particles. light (figure 34). They are always accompanied by a
Also worth mentioning are sulfides assuming a decrepitation halo where sulfide material has leaked
negative crystal shape. These inclusions are dark out into the surrounding corundum host. The nega-
black in darkfield illumination but may display a tive crystal morphology and observation of a
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 27
A B
C D
E F
Figure 33. Inclusions in natural-color (unheated) secondary Montana sapphire. A: Mica inclusions in a Rock Creek
sapphire. B: Missouri River sapphire with an unusual multiphase inclusion composed of mica, spinel, and other
unidentified phases. C: Two negative crystal inclusions with a partially healed decrepitation halo in a Missouri
River sapphire. D: Field of glassy melt inclusions in a Rock Creek sapphire. E: Single glassy melt inclusion with a
decrepitation halo in a Rock Creek sapphire. F: Glassy melt inclusion breaking the surface of a Missouri River sap-
phire. Photomicrographs by Nathan Renfro (A and B) and Aaron Palke (C–F); fields of view 2.09 mm (A), 1.31 mm
(B), 2.34 mm (C), 0.71 mm (D), 1.26 mm (E), and 0.71 mm (F).
polyphase mineral assemblage by SEM analysis sug- present during sapphire formation in addition to the
gests that these are an additional type of melt inclu- more silica-rich melts described above. In the au-
sion. In this case, a sulfide melt must have been thors’ experience, these sulfide melt inclusions are
28 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
A B
C D
Figure 34. Inclusions in natural-color (unheated) secondary Montana sapphire. A: Sulfide inclusion in a Missouri
River sapphire, shown in darkfield illumination. B: The same sulfide inclusion as in A, but with fiber-optic illumi-
nation. C: Sulfide inclusion in a Missouri River sapphire with a decrepitation halo where molten sulfide material
leaked out into a fracture in the corundum host. D: Field of sulfide inclusions in a Missouri River sapphire. Pho-
tomicrographs by Aaron Palke; fields of view 1.26 mm (A–C) and 4.79 mm (D).
seen almost exclusively in sapphires from Missouri medium-saturation pastel hues of blues, greens, yel-
River and Dry Cottonwood Creek, though they are lows, oranges, purples, and pinks. Beyond the initial
not common even then. Although sulfide inclusions impression from the bodycolor, one may find evi-
have been noted in a few Rock Creek sapphires (J.I. dence to separate these sapphires down the ocular
Koivula, pers. comm., 2022), screening of thousands barrel of a microscope. Umba sapphires especially
of samples by the authors has not identified this in- tend to have distinct inclusion features, the most
clusion in Rock Creek sapphire. common of which is heavy, repeated twinning.
Under cross-polarized light, the variously twinned
Inclusions/Microscopic Observations of Other Non- sectors may create a unique mosaic of colors (figure
Classical Sapphires. The sapphires most likely to be 35A). The boundaries between twinned sectors are
confused with Montana sapphire are those from often prominent and may be filled in with some sec-
Songea in Tanzania. Sapphires from Umba in Tanza- ondary aluminum oxy-hydroxide minerals (figure
nia may also show some generally similar character- 35B). Fields of clustered and single zircon inclusions
istics, but the inclusions are generally distinct are quite common in Umba sapphires (figure 35C).
enough to clearly separate them from secondary Dense aggregations of silk are not as common as in
Montana sapphires. The first thing one might notice Montana sapphires; however, the silk that can be
is the overall similar color range among all these de- seen often takes on a platy but very angular appear-
posits, which tends to include light-toned, low- to ance (figure 35, D–F).
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 29
A B
C D
E F
Figure 35. Typical inclusions in Umba sapphires. A: Multiple twinned sectors in cross-polarized light. B: Secondary
aluminum oxy-hydroxide minerals formed in the intersection of twins. C: Clusters of zircon inclusions. D:
Platelet-like reflective particles with iridescent thin-film interference colors using fiber-optic illumination. E:
Platelet inclusions. F: Silk in an Umba sapphire, from elongate needles to platelet-like inclusions. Photomicro-
graphs by Aaron Palke (A, B, D, and F), Charuwan Khowpong (C), and Ungkhana Atikarnsakul (E); fields of view
3.57 mm (A), 1.42 mm (B), 2.90 mm (C), 2.34 mm (D), 4.64 mm (E), and 2.90 mm (F).
Songea sapphires may have inclusion features blocky to angular or needle-like protogenetic rutile
that could look somewhat similar to secondary Mon- inclusions (figure 36, A and B). The silk in some
tana sapphire inclusion features. Often seen are Songea sapphire can somewhat resemble the silk in
30 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
A B
C D
E F
Figure 36. Representative inclusions in Songea sapphires. A: Protogenetic rutile inclusions with lobe-shaped
fringes. B: Two slender rutile inclusions. C: Typical pattern of rutile silk in a Songea sapphire, including sparsely
distributed medium to long silk and billowy clouds of particles. D: Small rutile dust and needles alongside
unidentified colorless crystals. E. Reflective silk and platelet particles. F. Reflective, scattered silk and particles.
Photomicrographs by Aaron Palke (A–C, E, and F) and Nathan Renfro (D); fields of view 1.26 mm (A and B), 2.34
mm (C), 1.79 mm (D), 1.76 mm (E), and 2.34 mm (F).
Montana sapphire. However, it is generally much (figure 36, C–F). Songea sapphire generally does not
more sparsely distributed and may appear in some- have the well-formed hexagonal bands of silk seen in
what randomly placed patches and as flecks of silk the Montana sapphire.
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 31
TABLE 1. Comparison of trace element compositions (in ppma) of sapphires from Montana’s secondary
sources and other deposits.a
Number of
Mg Ti V Cr Fe Ga
samples
Secondary
Montana 31 29 3 6 1600 13
51
(blue, green, (8–111) (3–109) (1–9) (bdl–43) (610–2750) (7–18)
yellow, colorless)
Secondary
Montana 25 29 6 742 1900 15
22
(pink sapphire (11–49) (9–81) (1–27) (32–2400) (620–2960) (11–20)
and ruby)
Myanmar 41 53 6 31 928 24
219
(various colors) (bdl–1510) (6–1018) (bdl–73) (bdl–1260) (172–3041) (5–82)
Detection limits
0.1–0.3 0.5–2.0 0.03–0.2 0.06–1.3 1–5 0.03–0.07
(ppma)
a
Averages are shown first, with the full range given in parentheses.
b
bdl = below detection limit
Trace Element Chemistry. Sapphires from the sec- (2007) as well as the Cr/Ga vs. Fe/Ti diagram of
ondary Montana deposits are classified by gemolo- Sutherland et al. (1998).
gists as “non-classical” sapphires. In essence, this The general trace element characteristics of the
means they are distinct from both the typical meta- secondary Montana sapphire deposits are summa-
morphic sapphires (from Myanmar, Sri Lanka, Mada- rized in table 1, where they are broadly compared
gascar, and Kashmir) and the typical magmatic, with sapphires from other deposits. Note that the
basalt-related sapphires (from Australia, Thailand, trace element chemistry of Montana’s three sec-
Cambodia, Nigeria, and Ethiopia). Their inability to ondary deposits broadly overlaps except for a few
fit into the standard metamorphic/magmatic di- very high-titanium Rock Creek sapphires, so they
chotomy is also seen in their trace element chem- will be considered together here as a single group.
istry. As is typical for non-classical sapphires, the There is some degree of overlap between the Mon-
secondary Montana sapphires have relatively high tana sapphires and a small subset of higher-iron
iron contents, suggesting a magmatic origin, while sapphires from the classical metamorphic deposits
the relatively low-gallium, higher-magnesium con- of Madagascar and Myanmar (figure 37); however,
tents and low-gallium/magnesium ratios suggests a sapphires from these deposits can generally be dis-
metamorphic origin. This discrepancy was pointed tinguished by careful observation of their inclusion
out in Palke et al. (2017), which showed that the characteristics (Palke et al., 2019). The sapphires
Montana sapphires plot in both the metamorphic that are more likely to be confused with the sec-
and magmatic domains in the Fe vs. Ga/Mg and Fe- ondary Montana sapphires are those from Umba
Mg×100-Ti×10 discriminant diagrams of Peucat et al. and Songea in Tanzania. There is broad overlap in
32 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Fe VS. Ga
19
17
13 typical metamorphic
blue sapphires. There is
overlap in the chemistry
11 with some Burmese and
Madagascar sapphires
9
and some minor overlap
with Sri Lanka.
Secondary Montana
Burma (Myanmar)
7
Madagascar
Sri Lanka
5
500 1000 1500 2000 2500 3000
Fe (ppma)
most trace elements for these deposits (figure 38). consistently be used for separating the Montana
Iron contents are higher on average for Songea, and sapphires. But for Montana sapphires occurring in
gallium contents of some Umba sapphires are colorless, green, blue, and yellow ranges, the trace
much higher, but overall these elements cannot element vanadium is a useful identifier. In partic-
Mg VS. Ti
120
Secondary Montana
(blue, green, yellow, colorless)
100 Secondary Montana
(pink, red)
Songea, Tanzania
80 Umba, Tanzania Figure 38. Plot of Mg vs.
Ti (in ppma) of the sec-
ondary Montana sap-
Ti (ppma)
20
0
0 20 40 60 80 100 120
Mg (ppma)
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 33
V VS. Fe
4000
Secondary Montana
(blue, green, yellow, colorless)
3500
Secondary Montana
(pink, red)
Figure 39. Plot of V vs.
3000 Songea, Tanzania
Fe (in ppma) of the sec-
Umba, Tanzania
ondary Montana sap-
2500 phire compared to other
deposits whose stones
Fe (ppma)
0
0 10 20 30 40
V (ppma)
ular, the vanadium vs. iron plot can separate most Emmett and Douthit’s technology was used to heat
Montana sapphires from Umba and Songea sap- the production of the American Gem Corporation
phire (figure 39). The caveat is that this does not in the 1990s and is currently employed by a small
apply to pink sapphire and ruby from Montana, handful of heat treatment facilities in the United
which have higher vanadium concentrations that States.
overlap with sapphire from Songea and Umba. This section chronicles the journey of several sap-
phire wafers through the heat treatment process with
Heat Treatment of Montana Sapphires. The previous careful documentation of their inclusions and spec-
section outlined various internal characteristics with troscopy before and after heating. Additionally, the
an eye toward establishing the provenance of un- samples were cut as oriented wafers with the c-axis
heated Montana sapphire from the Rock Creek, Mis- (or the optic axis) perpendicular to the plane of the
souri River, and Dry Cottonwood Creek deposits. wafer. This allows for only the o-ray spectrum to be
However, the majority of these sapphires entering the collected, while the extraordinary ray (e-ray) spec-
market have been heat treated at high temperatures trum cannot be observed. Note that this section is not
to improve their color, making them more desirable meant to be an exhaustive review of the heat treat-
for use in jewelry. This treatment fundamentally al- ment process for Montana sapphires, but is intended
ters the sapphires’ internal characteristics as well as to give readers an overview of key features that can
their spectroscopic properties. identify heat-treated Montana sapphires and to
It is important to note that, due to their unique demonstrate the effects of heat treatment on stones
chemistry, Montana sapphires require specialized that are commercially available. More technical de-
and carefully controlled heating environments that tails about the heat treatment process can be found
can typically be obtained only in modern resistance- in Emmett and Douthit (1993). The first three exam-
style furnaces. The specific technical requirements ples were heated by Dale Siegford of the Sapphire
for the heat treatment of Montana sapphire were re- Gallery in Philipsburg, Montana, and conditions of
alized in the pioneering scientific work of Emmett heating were not disclosed. The fourth and fifth ex-
and Douthit (1993). These involve careful control of amples were heated at GIA’s experimental heat treat-
not only heating temperatures and duration but also ment facility with carefully controlled conditions
oxidation environments using gas-mixing furnaces. described below.
34 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 40. The Rock
Creek sapphire in exam-
ple 1, measuring 9.5 ×
8.2 mm, before (left)
and after (right) heat
treatment shows the
blue coloration intro-
duced during treatment.
The gray circle on the
left shows the position
of the UV-Vis spectro-
scopic measurement.
Photos by Aaron Palke.
Example 1: Colorless and Cloudy to Blue. The first bands at 377, 388, and 450 nm related to Fe3+ and a
example illustrates the most advantageous outcome gradual upward slope from the near-infrared to the
for heat treatment of Montana sapphires. The stone ultraviolet region, caused by scattering of light from
was initially colorless but quite cloudy and included the rutile silk. The most obvious change caused by
(figure 40, left). The transmitted light photo of the heating is the creation of broad, intense absorption
unheated stone shows dense, hexagonal bands of ru- bands at 580 and 880 nm. The 580 nm band is re-
tile silk that scatter light, creating brown to yellow- sponsible for the stone’s blue coloration, as it absorbs
ish patches. While some unheated Montana sapphire most of the red light passing through by way of the
can be cut into exceptional colorless or slightly gray- excitation of an intervalence charge transfer (IVCT)
ish gems, this stone’s cloudiness makes it undesir- between Fe2+ and Ti4+ (Dubinsky et al., 2020). This
able for faceting. However, heat treatment causes a band increases in intensity as rutile silk is dissolved
dramatic change in the sapphire’s appearance, creat- into the corundum structure, where the titanium
ing a rich blue coloration where there were once ions introduced can pair locally with iron ions in a
patches of cloudy silk (figure 40, right). charge-balancing substitution of Fe2+ +Ti4+ for two
The change in color is also seen in the UV-Vis spec- ions of Al3+. The origin of the 880 nm band is not well
tra of this sapphire before and after heating (figure 41). understood but may be related to clusters of Fe2+, Fe3+,
The unheated sapphire showed narrow absorption and/or Ti4+ cations in the corundum structure
UV-VIS SPECTRA
14 Unheated
Heated
ABSORPTION COEFFICIENT (cm–1)
12
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 35
A B C
Figure 42. Example 1 before heat treatment under fiber-optic illumination (A), after heat treatment under fiber-
optic illumination (B), and after heat treatment under diffuse transmitted illumination (C). Photomicrographs by
Aaron Palke; field of view 4.08 mm.
(Hughes et al., 2017). Of particular note is that while ture of long needles as well as clouds of smaller par-
unheated blue Montana sapphires have a UV-Vis ticles either aligned with the hexagonal growth pat-
spectrum reminiscent of a typical metamorphic blue terns of the corundum or forming less-regular
sapphire, with an 880 nm band that is less intense patterns not ostensibly constrained by the corundum
than the 580 nm band (Palke et al., 2019), this heated lattice (figure 42A). Also seen are some reflective
blue Montana sapphire has a UV-Vis spectrum that platelet inclusions at the top left and bottom center
resembles a magmatic, basalt-related blue sapphire, of figure 42A. The heated stone still shows signifi-
with an 880 nm band that is more intense than the cant scattering of light from these rutile particles
580 nm band. This “reversal” of the UV-Vis spec- using fiber-optic illumination, indicating that the
trum in heated sapphire has been documented by particles have not fully dissolved into the corundum
both Emmett and Douthit (1993) and Hughes and structure. The long rutile needles have been com-
Perkins (2019), and it should provide the basis for pletely destroyed by heat treatment, but the overall
careful application of this classification scheme for pattern and distribution of smaller, cloudy rutile par-
heated blue sapphires. The other notable difference ticles has not changed dramatically (figure 42B).
for the heated sapphire is the decrease in absorption More conclusive evidence of heat treatment comes
in the near-UV and blue/green region of the spectrum from observing the distribution of blue coloration
from about 350 to 500 nm. This is caused by the dis- seen using diffuse transmitted illumination (figure
solution of rutile particles into the corundum struc- 42C) and comparing it to the distribution of incom-
ture and the consequent reduction in light scattering, pletely dissolved rutile inclusions (figure 42B). The
which enhances the blue coloration caused by the blue coloration in this sapphire shows a nearly exact
Fe2+/Ti4+ IVCT. correlation with the incompletely dissolved rutile
Finally, evidence of heat treatment can be found clouds, providing conclusive evidence of high-tem-
through careful microscopic observation. The pris- perature heat treatment. Also notable is that with
tine, unaltered silk in the unheated stone is a mix- the use of intense fiber-optic illumination, the blue
36 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
UV-VIS SPECTRA
ABSORPTION COEFFICIENT (cm–1) 20
Unheated, rim Unheated, core
Heated, rim Heated, core
Figure 44. UV-Vis spec-
15 tra of example 2 in its
unheated and heated
state. Two spectra were
10 collected in both states
in the core and rim of
the crystal demonstrat-
5
ing the creation of blue
coloration after heat
treatment.
0
300 400 500 600 700 800 900 1000
WAVELENGTH (nm)
coloration does seem to emanate from the especially heated core also has a pronounced rise in absorption,
dense cloudy regions such as the sector seen in the and its decrease in wavelength from the near-IR to the
top center of the photomicrograph in figure 42B. near-UV is caused by scattering from the densely con-
centrated rutile silk particles. After heating, the 580
Example 2: Brownish Blue to Blue. Our second ex- nm band increases dramatically in the core and slightly
ample involves a sapphire with a fairly well-devel- in the rim. Increased clarity (and decreased scattering)
oped blue coloration in its unheated state. However, is also important for improving the blue color in the
the extremely dense, cloudy nature of this stone, es- core, as there is also a significant decrease in absorption
pecially in its core, would have made it unsuitable in the ~350–500 nm region caused by dissolution of
for faceting. In this stone, the silk lends a brown col- light-scattering silk. Similar to example 1 above, the
oration. As shown in the before/after photos taken heated stone has what would appear to be a magmatic,
with diffuse transmitted light (figure 43), these basalt-related blue sapphire absorption spectrum, with
brownish cloudy regions take on an intensely satu- the 880 nm band more intense than the 580 nm band.
rated blue color after heat treatment. This is in contrast to the ostensibly metamorphic blue
This intensification of blue color can also be seen sapphire spectrum in the unheated stone.
in the UV-Vis spectra collected in two spots in the Finally, microscopic observations are useful for
core and rim of the sample before and after heating. identifying the high-temperature heat treatment of
In the unheated state, both the core and rim have a no- this sapphire. The unheated sapphire shows an ex-
ticeable broad absorption band at 580 nm related to tremely dense concentration of silk, largely com-
Fe2+/Ti4+ IVCT as well as narrow Fe3+-related absorption posed of medium to long needles, especially in the
bands at 377, 388, and 450 nm (figure 44). The un- core (figure 45A). The long needles have become par-
Figure 45. Example 2 before heat treatment with fiber-optic illumination (A), after heat treatment with fiber-optic
illumination (B), and after heat treatment with diffuse transmitted illumination (C). Photomicrographs by Aaron
Palke; field of view 4.79 mm.
A B C
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 37
Figure 46. The Rock Creek
sapphire in example 3,
measuring 9.5 × 9.2 mm,
before (left) and after
(right) heat treatment
shows creation of blue
color by heat treatment.
The gray circle on the left
shows the position of the
UV-Vis spectroscopic
measurement. Photos by
Aaron Palke.
tially dissolved into the corundum in the heated sap- color is, perhaps, less obvious from the UV-Vis spec-
phire (figure 45B). The use of fiber-optic illumination tra (figure 47). The absolute intensity of absorption
reveals that the silk has not completely dissolved and at 580 nm is not significantly different before and
can still scatter light quite intensely. Importantly, in after treatment. The main difference is the decreased
the heated stone, the light scattering off the remnant absorption between ~350–500 nm caused by reduc-
clouds has a distinct blue color as a result of the tion in scattering when the fine rutile silk is dis-
leaching of Ti4+ ions locally into the corundum. The solved into the corundum, allowing more blue light
correlation between dense blue coloration and the to be transmitted. While not as obvious, the 580 nm
remnant rutile clouds can be seen more clearly with band likely becomes more intense as well, although
the use of diffuse transmitted illumination (figure its increased intensity may be masked by the de-
45C), clearly demonstrating heat treatment. crease in absorption related to scattering. Note that
while the 880 nm band does increase after heating,
Example 3: Light Blue to Deeper Blue. The next ex- this change is not significant enough to make it more
ample involves a light blue sapphire with sparse silk intense than the band at 580 nm.
arranged in a hexagonal pattern, which is made ob- Microscopic observation reveals significant alter-
vious in diffuse transmitted light by the brownish ation of the rutile silk upon heating. Before heating,
coloration of the silk. Heat treatment increased the the silk was composed of a mixture of long, medium,
blue coloration by dissolving some of this silk into and short needles and particles arranged in a hexago-
the corundum structure (figure 46). The change in nal pattern (figure 48A). After heating, the long and
UV-VIS SPECTRA
20
Unheated
ABSORPTION COEFFICIENT (cm–1)
Heated
15
0
300 400 500 600 700 800 900
WAVELENGTH (nm)
38 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
A B C
Figure 48. Example 3 before heat treatment with fiber-optic illumination (A), after heat treatment with fiber-optic
illumination (B), and after heat treatment with diffuse transmitted illumination (C). Photomicrographs by Aaron
Palke; field of view 2.34 mm.
medium silk are completely decomposed and the nificant rutile particles and silk was heated at
hexagonal clouds of particles are made up of very fine, 1700°C for 12 hours in a reducing atmosphere com-
dusty particles (figure 48B). Also notable is the small posed of 0.33 atm partial pressure of H2 and 0.67 atm
inclusion in the core with the concentrically aligned partial pressure of CO2. The sapphire was cooled
decrepitation halo (figure 48A, top center). After heat- slowly at a rate of 4°C/minute. This was done twice
ing, the decrepitation halo has become filled with to ensure the sapphire reached a steady state at these
some residual material, likely from the melting or al- conditions. The same sapphire was heated again at
teration of the originally intact central inclusion. Fi- the same conditions but quenched rapidly by placing
nally, the most conclusive evidence of heat treatment it in a crucible affixed to an alumina rod that can be
comes from comparing the distribution of partially retracted from the bottom of the muffle tube. In this
dissolved silk using a fiber-optic light and blue patches way, the sapphire is cooled from 1700°C to about
of coloration using diffuse transmitted light (figure 1000°C in 1–2 minutes and then further cooled to
48C). The correlation between the remnant silk room temperature in roughly 15 minutes. The spec-
clouds and the blue zones of color allows for easy iden- tra and photos of the sapphire after various stages of
tification of heat treatment in this case. heat treatment demonstrate the deeper blue color of
the rapidly cooled sapphire compared to the slowly
Example 4: Effect of Cooling Rate. While the precise cooled heating (figures 49 and 50). When the sapphire
heating conditions for the above experiments are not is slowly cooled, the titanium dissolved into the
known, additional tests have been carried out at corundum can start to exsolve as rutile (TiO2) as the
GIA’s experimental heat treatment facility. In the solubility of titanium in corundum decreases with
first experiment, a cloudy, pale blue stone with sig- decreasing temperature. As the rutile particles pre-
Figure 49. The sapphire in example 4, measuring 8.1 × 6.5 mm: unheated (A), heated to 1700°C and slowly cooled
(B), and heated to 1700°C and rapidly cooled (C), showing a deeper blue color with rapid cooling. The gray circle
shows the area of analysis. Photos by Aaron Palke.
A B C
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 39
UV-VIS SPECTRA
14 Unheated
Heated, slow cool
Heated, rapid cool
12
ABSORPTION COEFFICIENT (cm–1)
0
350 450 550 650 750 850
WAVELENGTH (nm)
cipitate and grow during cooling, the titanium exits suggests either that rutile was never fully dissolved
the corundum lattice, causing a reduction in the into the corundum lattice at 1700°C or that even
Fe2+-Ti4+ intervalence charge transfer band and a re- with rapid cooling there was still some very rapid
duction in the blue coloration. Rapid cooling exsolution of rutile.
quenches in the high-temperature solubility of tita-
nium in the corundum lattice and retards exsolution Example 5: Creation of Trapped-Hole Coloration.
of rutile upon cooling. Note, however, that rapid For one final example, we consider two sapphires
cooling does not lead to complete dissolution of ru- with entirely different responses to heat treatment.
tile silk and particles in the sapphire, as seen in the Many Montana sapphires are heated to create or in-
photomicrographs in figure 51. The use of intense tensify yellow or orange color by creating what is re-
fiber-optic lighting shows that even the rapidly ferred to as a “trapped hole.” This trapped-hole
cooled sapphire has an abundance of light-scattering chromophore involves a Mg2+ atom substituting for
rutile particles. The presence of these rutile particles Al3+ with a missing electron on a nearby oxygen
Figure 51. Rutile silk and particles in example 4 in the unheated (A), heated (slowly cooled, B), and heated (rapidly
cooled, C) states showing the existence of rutile particles even in the heated and rapidly cooled sapphire. Photomi-
crographs by Aaron Palke; field of view 3.57 mm.
A B C
40 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
A B C
Figure 52. The Rock Creek sapphire in example 5, measuring 0.8 × 0.5 mm: unheated (A), heated to 1200°C in pure
O2 (B), and heated to 1700°C in pure O2 (C). The gray circle shows area of analysis. Photos by Aaron Palke.
anion for charge balance (a trapped hole). This leaves oxygen vacancies instead of the trapped hole on the
the oxygen anion with a charge of –1 and causes it to O– anion.
absorb light at 450 nm, creating intense yellow or or- Figures 52–55 show the results of an oxidizing
ange color (see Dubinsky et al., 2020). Some heaters heat treatment run on two sapphires, one from Rock
who specialize in treating Montana sapphire will Creek (figures 52 and 53) and one from Dry Cotton-
carry out what is referred to as a “fancy burn” in an wood Creek (figures 54 and 55). Both were heated
oxidizing atmosphere to bring out yellow and orange once at 1200°C in a pure O2 atmosphere for 12 hours,
hues. The creation of trapped-hole absorption centers then heated again at 1700°C in a pure O2 atmosphere
by heating Montana sapphires in an oxidizing envi- for 12 hours.
ronment was carefully documented by Emmett and The sapphire from Rock Creek developed an or-
Douthit (1993). ange core after heating in O2 at 1200°C (figure 52).
Many heated fancy-color sapphires will display an The UV-Vis spectrum shows this change, with an in-
intense yellow or orange core where the trapped-hole crease in absorption in the region from 350 to 500 nm
chromophore is developed. This heating needs to be (figure 53). The difference between the heated and un-
carried out in an oxidizing environment in order to heated spectra shows the creation of the trapped-hole
create a trapped hole. Heating in reducing environ- absorption band centered at around 480 nm. The neg-
ments can facilitate the charge balance of Mg2+ by ative dip in the difference spectrum centered at about
UV-VIS SPECTRA
18
Unheated
16 1200°C, 12h
1700°C, 12h
ABSORPTION COEFFICIENT (cm–1)
14 Difference
12
Figure 53. UV-Vis spec-
10 tra of example 5 from
Rock Creek: unheated,
8
heated to 1200°C for 12
6
hours in pure O2, and
heated to 1700°C in
4 pure O2.
-2
350 450 550 650 750 850
WAVELENGTH (nm)
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 41
A B C
Figure 54. The Dry Cottonwood Creek sapphire in example 5, measuring 7.2 × 6.7 mm: unheated (A), heated to
1200°C in pure O2 (B), and heated to 1700°C in pure O2 (C). The gray circle shows area of analysis. Photos by
Aaron Palke.
580 nm indicates that heating also reduced the Fe2+- in this sample by heating at the higher temperature
Ti4+ intervalence charge transfer absorption. Heating of 1700°C in pure O2 (figure 55). This sapphire also
at 1700°C resulted in a negligible change in color, pos- developed blue color in its rim during heating due to
sibly with a slight increase in the trapped-hole absorp- dissolution of rutile particles and introduction of Ti4+
tion band in the UV-Vis spectrum. cations into the corundum structure, leading to cre-
The sapphire from Dry Cottonwood Creek did not ation of Fe2+-Ti4+ IVCT chromophores.
develop the trapped-hole chromophore after heating The fundamental difference in the behavior dur-
at 1200°C (figure 54). The only change at this lower ing the oxidizing heat treatment is in the way excess
temperature was a lightening of the blue color due to Mg2+ cations are charge-balanced in the original un-
a reduction in the Fe2+-Ti4+ IVCT absorption (figure heated sapphire. The FTIR spectrum of the Rock
55). The trapped-hole chromophore is only developed Creek sapphire here contained the acceptor-domi-
UV-VIS SPECTRA
24
Unheated
1200°C, 12h
1700°C, 12h
ABSORPTION COEFFICIENT (cm–1)
19 Difference
-1
350 450 550 650 750 850
WAVELENGTH (nm)
42 MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023
Figure 56. Heat-treated Rock Creek sapphires; the largest rough stone weighs 4.62 ct. Photo by Jeff Scovil; courtesy
of Potentate Mining.
nated 3000 cm–1 series (the “Punsiri band”), which treating Montana sapphires from all three secondary
is caused by H+ cations charge-balancing excess Mg2+ deposits, Dr. Emmett has observed significant differ-
cations. This hydrogen is easily burned away at rel- ences in the way sapphires from these deposits react
atively low temperatures (i.e., 1200°C), leaving the to oxidizing heat treatment. Missouri River sapphires
Mg2+ to be charge-balanced by a trapped hole when do not have the acceptor-dominated 3000 cm–1 series
heated in an oxidizing environment (J.L. Emmett, in the infrared and therefore require high tempera-
pers. comm., 2022). The Dry Cottonwood Creek sap- tures in oxidizing conditions to develop trapped-hole
phire did not have the acceptor-dominated 3000 cm–1 coloration. On the other hand, Rock Creek sapphires
series in its FTIR spectrum, indicating that any ex- often have the acceptor-dominated infrared features
cess Mg2+ would have been charge-balanced by oxy- at 3000 cm–1 (see figure 23) and frequently react well
gen vacancies. Trapped holes in this case can only to an oxidizing fancy burn at temperatures as low as
be created by diffusion of aluminum vacancies into 1200°C. According to Dr. Emmett, a small propor-
the sapphire to annihilate oxygen vacancies, thereby tion of Dry Cottonwood Creek sapphires have the
allowing Mg2+ to be charge-balanced by trapped acceptor-dominated 3000 cm–1 features and will de-
holes instead of the oxygen vacancy (J.L. Emmett, velop yellow or orange color at 1200°C, but more fre-
pers. comm., 2022). But diffusion of aluminum va- quently these require higher temperatures around
cancies requires extreme temperatures and long 1700–1800°C.
heating times, which is why this is only seen in the
sapphire heated at 1700°C for 12 hours and not when CONCLUSIONS
heated at the lower temperature of 1200°C. Only a With large volumes of Montana sapphire being pro-
small number of Montana sapphires have been duced in consistent and reliable quantities (figure 56),
heated this way at GIA’s experimental heat treat- the secondary Montana sapphire deposits are some
ment facility so far. However, in many years of heat of the most important American gem mines in mod-
MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 43
Figure 57. A 2.02 ct un-
heated Montana sap-
phire featuring concave
faceting. Courtesy of
Derek Katzenbach.
ern times. The material fits a wide variety of market trace element chemistry, allowing the provenance of
demands, from heated goods under 1 carat size to these stones to be preserved and traced once the
rare, fine, unheated sapphires up to several carats. stones enter the gem and jewelry market. With the
Aggressive marketing by Potentate Mining and its af- wide range of colors produced, Montana sapphire is
filiates as well as by independent artisanal miners, an exceptionally versatile gem, finding a home in
especially through social media, has driven up inter- nearly any style of jewelry (figure 57). With large re-
est in these gemstones both domestically and in the serves remaining at Rock Creek, Missouri River, and
international gem and jewelry market. Identifying Dry Cottonwood Creek and their growing popularity
the origin and treatments for Montana sapphires can with consumers, Montana sapphire is likely to play
be relatively straightforward based on inclusions and an increasingly important role in the market.
ABOUT THE AUTHORS field at Eldorado Bar at Cass Thompson’s operation (Eldo-
Dr. Aaron Palke is senior manager of colored stone research, and rado Sapphire mine) and from Potentate’s operations at
Nathan Renfro is senior manager of colored stone identification, Rock Creek. Some Dry Cottonwood Creek samples were
at GIA in Carlsbad. Jeffrey R. Hapeman is president of Earth’s donated by Dr. John Emmett, who obtained them from the
Treasury (Westtown, Pennsylvania). Dr. Richard Berg is a research mining operations of American Gem Corporation in
geologist emeritus at the Montana Bureau of Mines and Geology 1994–1995. Dale Siegford provided samples for analysis
at Montana Tech of the University of Montana in Butte. and heat treatment services for some of the samples here.
Many thanks are owed to Dr. Keith Barron and Warren
ACKNOWLEDGMENTS Boyd of Potentate Mining for providing samples, informa-
Many samples containing prominent inclusions were sourced tion, and advice for this manuscript. The authors are grate-
from the inclusion collection of John I. Koivula. Samples from ful for thorough reviews by Dr. Emmett as well as two
GIA’s Colored Stone Reference Collection were collected in the anonymous reviewers.
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MONTANA SAPPHIRE FROM SECONDARY DEPOSITS GEMS & GEMOLOGY SPRING 2023 45
FEATURE ARTICLES
The morphology of Colombian emerald, including growth and dissolution features of their faces, gives insight
into growth and post-growth history of individual crystals. A collection of 15 isolated crystals and seven emeralds
in matrix was studied by optical methods. The authors observed layered growth of prismatic, dipyramidal, and
basal sectors that leads to crystals with prismatic to columnar or rarely pyramidal habit. In the latter case, pris-
matic growth sectors were not developed. The visual appearance of the crystal faces at the surface was influenced
by etch patterns with the formation of cavities, pits, pointed hillocks, and stepped grooves, followed occasionally
by layered overgrowth. Skeletal growth led to the formation of cavities in crystals, some of them resembling
empty cups with planar bottoms. In these crystals, the basal faces showed indentations or deep cavities, sur-
rounded by shells or rims of emerald, bound on both vertical surfaces by prism or dipyramidal faces. Emeralds
in the form of slightly conical empty tubes also belong to the latter group. Possible relationships to trapiche
emeralds and samples exhibiting the gota de aceite effect are discussed.
I
n general, the morphology of Colombian emerald slightly conical empty tubes (Klein, 1941)—or emer-
originating from different mines is rather simple alds in the form of prismatic, empty “cups” with pla-
and formed by a small number of external crystal nar bottoms (Weldon et al., 2016). In most references,
faces. We observe two dominant planes, the basal
pinacoid and the first-order hexagonal prism, occa-
sionally in combination with small second-order
hexagonal prism faces and first- and/or second-order
In Brief
hexagonal dipyramids (Goldschmidt, 1913; Schwarz • The surface texture of Colombian emerald crystals re-
and Giuliani, 2002; Moore and Wilson, 2016). The in- veals details about growth and post-growth history.
ternal growth pattern of such samples, which nor- • Several crystals show indications of natural etching in
mally show prismatic habit, consists of growth aggressive fluids, and some samples have undergone
planes parallel to the external crystal faces (Kiefert several subsequent growth and corrosion steps.
and Schmetzer, 1991). • In crystals with a conical shape, only basal and
Occasionally, natural emerald and beryl crystals dipyramidal growth sectors were developed.
show etching and dissolution features (an overview • Skeletal growth is observed in emeralds showing the
of the pertinent literature is given in box A). Other form of empty cups or emeralds with indentations on
the basal face.
growth features are due to skeletal and polygonal
growth of beryl crystals (see box B). Both growth fea- • Within the empty cups, polygonal growth of small
tures are related to the observations made in this ar- emerald columns is observed.
ticle for Colombian emerald crystals.
Rarely mentioned are emerald crystals with con-
ical habit (Johnson, 1961a,b)—or vasos in the form of such emeralds with conical habit (figure 1) or emer-
ald vasos or cups (figure 2) have been briefly men-
tioned or have only been pictured without
See end of article for About the Authors and Acknowledgments.
GEMS & GEMOLOGY, Vol. 59, No. 1, pp. 46–71,
considering a possible growth mechanism. In the fol-
[Link] lowing discussion, we will use only the term “cups”
© 2023 Gemological Institute of America for both slightly different variants.
Etch pits on basal, prismatic, and pyramidal faces of might show etch pits, other faces of the same crystal are
Colombian emerald have been described or depicted by completely free of such textures (Petersson, 1889;
a few authors (e.g., Honess, 1917, 1929; Medina et al., Arzruni, 1894; Vrba, 1895; Tschermak, 1897; Kohlmann,
1983; Moore and Wilson, 2016). Considering the min- 1908; Sinkankas, 1981).
eral beryl in general, various forms of tiny cavities or These generally observed features of etch patterns in
pits have been observed with different shapes reflecting beryls from numerous localities are consistent with the
the symmetry of the individual basal, prismatic, or results of etching experiments performed in the labora-
dipyramidal crystal faces (figure A-1). In addition, the tory (Taube, 1895/1896; Feklichev, 1963). Such experi-
shape of etch patterns varies between samples from dif- mental processes were done in various acidic or basic
ferent localities (Kurumathoor and Franz, 2018). It has solutions, but normally only for periods of seconds to
also been mentioned that while some faces of crystals minutes.
m a
Figure A-3. Left: A heavily etched Colombian emerald crystal from Muzo measuring 27 mm in length. The basal pinacoid
is completely dissolved, leading to numerous pointed hillocks; the growth sectors related to the a prism faces are optically
reflective. Photo by Jeff Scovil. Right: Etched beryl crystal from Pont de Barost, Haute-Vienne, France, showing a com-
pletely dissolved basal face with numerous pointed hillocks. From Lacroix (1896).
c, m, a, s, p; Growth steps on
L 9.8, partly conical conical surface and on Groth tubes along the c-
8: Chivor — 1.61 ct 9
D 4.8–5.1 with tabular m faces of the tabular axis in tabular part
part part
Growth steps on m, Residual dark gray
L 20.8, c, m, a, s, p;
9: Muzo (?) — 10.76 ct finer structures on the (carbonaceous) material 10
D 10.8–12.1 conical
conical part in cavities
Indentations on c,
Crystal on gray L 15.5, c, m, a, u, p, s; Associated minerals:
11: Chivor 43.2 g growth steps on 12A
shale, 56 × 37 D 3.5–4.1 columnar calcite, pyrite
prismatic faces
aggregate of 11
Crystals on Indentations on c of all
parallel crystals; c, m, a; Associated minerals: 12B and 13,
12: Chivor dark gray shale, 50.0 g crystals, growth steps
largest L 12.5, columnar pyrite, dolomite, albite A and D
51 × 37 on prismatic faces
D 5.0–6.5
earthed within this period or in the last few years— According to the general knowledge of emerald
some of them might originate from Colombian col- formation in the various Colombian deposits, all of
lections, with samples being kept there for several the emeralds grew in cavities and were removed by
years or even decades before they were offered for sale. the miners, either as isolated crystals or in matrix.
Deep indentations on c,
L 37.4, c, m, a, i, f, k;
15: Chivor — 17.24 ct growth steps on Color zoning 15
D 6.6–7.1 columnar
prismatic faces
Irregularly shaped
L 10.8, c, m, a, s, p; Open cup, growth steps
16: Chivor — 6.37 ct hillocks and columns in 16
D 7.3–8.7 columnar on prismatic faces
cup
cup 1: L 5.5,
D 2.5–3.0
cup 2: D 3.0 Associated minerals:
Five crystals
albite, calcite, pyrite;
on black shale; crystal 1: L 12.0, Open cups, growth
17: Chivor 4.5 g c, m; columnar irregularly shaped 2 and 17
26 long, 11–20 D 2.0 steps on m
hillocks and columns in
wide
crystals 2 and 3 both cups
are smaller
crystal 3: L 3.8
c, m, a;
Slightly conical tube
L 14.4, elongated Etch pits and grooves
22: Chivor — 1.63 ct along the c-axis through 21 and 22
D 3.4–4.4 columnar, on prismatic faces
the complete crystal
slightly conical
a
L represents the length of the emerald crystal, D represents measurements of diameters between two m prismatic faces.
b
Weights of samples with emerald crystals in matrix are given in grams; weights of isolated emerald crystals are given in carats.
c
Based on a cell with a:c ratio of 1:0.996; basal pinacoid c {0001}, first-order hexagonal prism m {101̄0}, second-order hexagonal prism a {112̄0}, dihexagonal prism
i {213̄0}, first-order hexagonal dipyramids p {101̄2} and u {101̄1}, second-order hexagonal dipyramids s {112̄2} and f {336̄2}, and dihexagonal dipyramid k {213̄1}.
For the evaluation of growth history, it is impor- ally, and crystal faces were determined by goniomet-
tant to look at all morphological features of a sample ric measurements and/or by the measurement of an-
as a summary and not only at isolated crystal faces. gles between crystal faces in the microscope.
The morphology of the samples was examined visu- The samples were studied exclusively by nonde-
m a m
Figure 3. Morphology of
c c Colombian emeralds
C D observed in the present
study. A–D: Most sam-
s s ples show dominant m
p u p
prism and basal c faces;
occasionally we also
observed smaller a
m a m a prism faces in combina-
tion with s, p, and u
hexagonal dipyramids.
E: Furthermore, two of
the crystals showed ad-
ditional small i prism
faces in combination
with f and k dipyra-
mids. Drawings by K.
Schmetzer.
c
E
p k s
f
m a i
structive methods, especially by optical microscopy liquid. For such rare materials (isolated emerald crys-
at low magnification (up to 80×). A few transparent tals or matrix specimens), no destructive techniques
samples of appropriate size were also examined in (e.g., slicing or polishing of the crystals) could be ap-
immersion using benzyl benzoate as the immersion plied nor any coating of the samples for an investiga-
Figure 4. A and B: In sample 1 (11.8 mm in length), stepped surface structures on different prismatic m faces of a
Colombian emerald crystal represent layered growth in subsequent growth steps. C: Best observation of such lay-
ered stepped growth structures is achieved in reflected light. Photos by G. Martayan (A and B) and K. Schmetzer
(C; field of view 6.0 mm).
A B C
Figure 5. Sample 2 (18.0 mm in length), a columnar emerald that has been heavily corroded by natural etching. A:
The basal plane shows irregularly shaped openings to larger cavities below this face. B: The m prism planes show
etch structures, especially irregularly oriented grooves between hillocks. C: Details of the etch structures with
grooves and hillocks, seen on the m prism face in image B, which are covered by micro-steps as seen in reflected
light. Photos by K. Schmetzer; field of view 3.5 mm (C).
Sinkankas, 1981; Sunagawa and Urano, 1999; Suna- Between the deep irregular grooves, small hillocks are
gawa, 2003; Demianets et al., 2006). observed that show micro-steps on the surface (figure
5C). These micro-steps resemble the pattern pro-
Characteristics of Individual Groups of Samples with duced as fine structure in etch pits by artificial disso-
Respect to Growth or Post-Growth Surface Patterns. lution of beryl crystals (see box A). It is unknown and
Emeralds with Dissolution Features. A group of must be examined in additional samples, which are
three samples with “common” habit (samples 2, 3, not available at the moment, whether this pattern
and 4) showed pronounced dissolution features with and the form of the irregularly shaped grooves are re-
partially dissolved (corroded) crystal surfaces. In the lated to the common inclusion features of Colombian
groups describing samples with extraordinary and emerald (e.g., feathers and healed fractures).
rare habits in the following sections, some emeralds Sample 3 with tabular habit shows a completely
that have undergone dissolution are also mentioned. and irregularly dissolved surface of the m prism, but
To understand the various observations, one general the smaller a prism is not corroded (figure 6A). Only
aspect should be mentioned at the beginning of this small parts of the original surface of the m prism are
section: Some of the crystals examined in this study still present, reflecting under appropriate illumina-
show strong etching and dissolution features only at tion (figure 6B). In this case, we can speak of a pre-
part of the surface. This indicates that only these ferred dissolution of the m prism compared to the a
parts of the emerald crystals were exposed to the ag- prism face. The basal face shows irregularly termi-
gressive dissolution fluid and the other parts of the nated openings to deep cavities, but part of this face
crystals were shielded from the fluid. It can be as- contains no dissolution features (figure 6C), and
sumed that such shielding processes were caused by therefore it might be concluded that this face was
different minerals of the assemblage found in Colom- shielded by minerals from the dissolution fluid.
bian emerald deposits, which were in close contact Sample 4 shows long prismatic habit with first-
with the emeralds’ as-grown surfaces (crystal faces). and second-order m and a prism faces (figure 3A). To-
In the present state, these minerals are at least par- ward one end of the crystal, the prism faces show
tially dissolved or broken away, now exposing the growth steps of an almost undistorted surface (figure
crystal faces of the emeralds for visual examination. 7A). This part represents about one-third of the
Sample 2 (figure 5A) with columnar habit (see fig- length of the crystal. The remaining part is exten-
ure 3B) shows distinct corrosion features. The basal sively etched, deeply corroded on m faces and to a
face reveals several irregularly shaped openings to a much lesser extent on a prism faces (figure 7, A and
cavity below this plane, which is larger than the open- B). In some areas, the m prism faces are completely
ings, extending widely into the crystal. Prism faces dissolved to an area with numerous grooves and
are completely covered by etch structures (figure 5B). hillocks. In contrast, we observe highly reflective
Figure 6. A: Sample 3 (23.6 mm in length), a heavily corroded emerald crystal with a completely dissolved surface
related to the m prism face, but with a small protruding area related to the a prism that is almost free of corrosion.
B: Only small areas of the original surface of the m prism are still reflective. C: The c basal pinacoid reveals irregu-
larly shaped holes leading to cavities below this face. Photos by G. Martayan (A and C), and K. Schmetzer (B);
field of view 7.6 mm (B).
ledges of the a prism protruding from the dissolved concluded that samples 2–4 have undergone a heavy
m growth sectors (figure 7B). This indicates that, as natural dissolution process in which the original sur-
also observed in sample 3, the a prism sectors were faces of the crystal faces were partially or completely
less intensely corroded. At the end, one basal pina- dissolved by natural etching. In other words, the pat-
coid is only influenced slightly or not at all by corro- terns observed in our Colombian samples are related
sion, while the other basal plane on the other end of to intense natural etching processes causing at least a
the crystal is heavily dissolved (figure 7, C and D). partial dissolution of the as-grown crystal faces and
Evaluation. Comparing these observations with creating deep cavities and irregular grooves between
descriptions from the known literature (box A), it is hillocks with stepped surfaces. All three crystals show
Figure 8. A: Emerald
crystals with pyramidal
or partly pyramidal
habit: sample 5 (left,
10.0 mm in length),
sample 7 (center, 8.8
mm in length), and
sample 6 (right, 8.8 mm
in length). B: Surface
texture of the pyrami-
dal emerald crystal
(sample 5) showing
growth lines related to
the basal pinacoid c
(center) and pyramidal
faces p (left and right).
C: Complex surface tex-
ture of a partly pyrami-
B C dal, partly prismatic
crystal (sample 7)
showing a complex pat-
p tern related to pyrami-
c
dal faces (lower part)
and to basal, pyrami-
p dal, and prism faces
p (upper part). The
growth direction of the
c crystals shown in A–C
is always from the bot-
tom to the top. Photos
by G. Martayan (A) and
K. Schmetzer (B and C);
fields of view 2.4 mm
(B) and 2.4 mm (C).
c
p
various dissolution features on different surfaces. Referring to the observations made in this study
Sample 4, for example, shows heavy dissolution from for samples 5–10, the authors must underscore that
one end with a dissolved basal c face to almost two- with the optical methods applied, we only can de-
thirds of its length, while the other end with basal c scribe the features representing the last stage of
face to about one-third of its length is barely affected. growth and/or dissolution.
In samples 2 and 3, it seems that the basal c faces were Three relatively small emerald crystals, desig-
partially shielded from the dissolution fluid. nated samples 5, 6, and 7, show the habit of a six-
An emerald with pointed forms (sample 10) sided pyramid or the habit of a six-sided pyramid
caused by natural etching will be described in the combined with a six-sided prism (figure 8A). The sur-
next section. face texture of the pyramidal sample 5 shows growth
steps related to basal and pyramidal growth layers
Emerald Crystals with Conical Habit or Conical (figure 8B). The basal growth layers are visible as stri-
Zones. Several samples showed, at least partly, a con- ations perpendicular to the c-axis, which indicate al-
ical habit, comparable to six-sided pyramids. ternating basal and dipyramidal faces. The surface
A B
A B
Figure 10. A: Sample 9
s (20.8 mm in length), an
emerald crystal with coni-
cal shape, with basal pina-
coid c, small m prism
faces, and hexagonal s
dipyramids. B: Growth
steps on the surface of one
of the m prism faces,
viewed almost perpendicu-
lar to the c-axis. C:
Hillocks with fine micro-
C D steps between irregularly
shaped groves on the sur-
face of the conical part. D:
Residual dark gray car-
bonaceous material cap-
tured in indentations on
the surface of the conical
part. Photos by K. Schmet-
zer; fields of view 4.5 mm
(B), 3.5 mm (C), and 7.6
mm (D).
dipyramidal growth sectors were developed, but growth step (see references cited above). Skeletal
without development of related prismatic growth growth (see box B and examples below) with pointed
layers. These growth stages without formation of pyramids and sharp hillocks has never been men-
prismatic growth layers apply at least to part of the tioned in any beryl and is therefore considered very
crystal’s growth history. unlikely for this morphological structure.
In the tabular area of sample 8, we observe growth After corrosion, we observe several subsequent
channels parallel to the c-axis, which were not seen growth steps, in which an area with prismatic growth
in the tapered part of the crystal. The diameter of the layers and the conical zone with basal striations were
tabular area is larger than the diameter of the conical developed. Obviously, in one of these growth steps,
part at its upper end. This might indicate a later par- only basal growth layers without prismatic areas were
tial overgrowth of a crystal with conical habit and, formed. It is not completely understood whether the
in this later growth period, the development of a tab- prismatic m growth sectors in the lower part of the
ular area, on top of the tapered part of the crystal (see crystal were grown before or after the conical zone
again figure 9). with tapered surface of the crystal (see again figure 11).
Sample 9, at its wider end, has a short prismatic
area and a long, tapered cone. This cone shows dis- Emeralds with Incomplete Growth of the Basal
solution features on its surface. These features indi- Face. Several variants of incomplete growth of the
cate an etching process of the conical part after basal pinacoid were observed.
crystal growth and a subsequent growth step with Samples 11, 12, and 13 show incomplete growth
the formation of prismatic layers at the end of the of the basal face c, a pattern that could be described
crystal (see again figure 10). as resembling surface indentations. Sample 11 (figure
Sample 10 has likely undergone several growth 12A) is a single emerald crystal on matrix and reveals
and corrosion processes. The residual parts of pris- well-developed prism and pyramidal faces. Sample
matic a growth zones and the small pyramids or 12 (figure 12B) is an aggregate of approximately 11
hillocks forming the end of the conical part of the crystals, grown parallel to each other with somewhat
crystal indicate strong corrosion after an initial different lengths. All crystals of this aggregate show
Figure 12. Emeralds with surface indentations on the basal face, developed as either a single crystal (A: sample 11,
4.1 mm in largest diameter) or as aggregates of parallel emerald crystals (B and C: samples 12 and 13 with crystal
length up to 12.5 mm and 16.5 mm, respectively). Photos by G. Martayan.
incompletely developed c faces. Sample 13 (figure or other structures have different heights within the
12C) is similar to sample 12, but with three such ag- rim. In addition, all three samples have a step-like tex-
gregates consisting of approximately nine, eight, and ture on prism faces and no etch features. A represen-
three emerald crystals. All basal faces have a stepped tative example of that pattern is shown in figure 13D.
micro-texture consisting of numerous layers stacked Samples 14 and 15 show somewhat deeper inden-
parallel to the c-axis of the emerald crystal (figure 13, tations on the basal faces. Sample 14 has an almost
A–C). These structures occasionally end at the level continuous rim parallel to the basal face and inside
of the horizontal surface of the rim, but some columns several hillocks within the indentation zone (figure
A B
14, left). Part of these hillocks in the form of tiny first- and second-order prism faces in combination
columns end with faces parallel to the base (figure with first- and second-order hexagonal dipyramids
14, right), but lower than the horizontal surface of (figure 3C and figure 16, A and B). The m prism faces
the rim, which is formed by the incomplete basal are planar; no growth steps or etch features were vis-
face of the crystal. Sample 15, with similar appear- ible in the optical microscope with the magnification
ance, shows an almost colorless region that ends in applied. The wall thickness of the cup varies between
a basal face with indentations (figure 15A). The end 0.8 and 1.4 mm. Irregularly shaped hillocks or
of the crystal with these indentations is separated columns cover the bottom of the cup, which forms a
from the main part by a small zone with intense clear boundary with the other part of the crystal (fig-
green coloration (figure 15B). This demonstrates that ure 16C). In a view parallel to the c-axis, a micro-
at the beginning of the growth of this zone with a structure is observed forming a three-dimensional
length of about 1.5 mm along the c-axis, growth con- framework of walls, columns, and hillocks at the bot-
ditions were different compared to the earlier growth tom of the cavity (figure 16D). Part of the columns
stages. Hollow channels parallel to the c-axis are or irregular walls end in planar faces parallel to the
found in all parts of the crystal. The areas parallel to basal pinacoid (figure 16, A and B).
the basal face show growth steps (figure 15C). Sample 17 is a piece of black shale covered by al-
Several crystals were formed as “emerald cups.” bite, calcite, and pyrite crystals. Embedded in this
Sample 16 is a crystal with columnar habit in the matrix are five emerald crystals (figures 2 and 17A).
form of an open cup. The morphology consists of Two of these are columnar and hollow, forming deep
Figure 15. A: Sample 15 (37.4 mm in length), an emerald crystal with color zoning; at one end, the sample reveals a
continuous rim surrounding growth areas ending in small basal faces. B: Growth and color zoning (arrows) of the
crystal along the c-axis. C: Areas of the rim and small columns inside the rim with planes parallel to the basal pina-
coid appear bright in reflected light, viewed parallel to the c-axis. Photos by K. Schmetzer; field of view 3.6 mm (C).
A B C
cups with one open end (figure 17B). The cups have space of the cups with irregularly shaped planes.
a wall thickness of approximately 0.5 mm. The bot- Other planes at the ends of the tiny crystals in the
tom of each cup is covered with emerald hillocks or hollow cups reflect together with the residual basal
columns, which frequently end within the hollow face of the rims (figure 17C), indicating that some of
the hillocks or columns also end in faces parallel to the basal pinacoid, but holes are also developed in the
the basal pinacoid. The m prism faces of the cups largest p dipyramid (figure 18C). The cup’s wall
show growth steps (figure 17D). thickness ranges from 1.5 to 2.0 mm. Within the cup,
The three other emerald crystals are “common” a framework of irregularly shaped thin emerald walls
columnar crystals with prismatic and basal faces (fig- is present (figure 18, B and C). The main walls of the
ure 17A), which also show growth steps on m prism inner surface of the rim are oriented parallel to prism
faces and no etch features (figure 17E). faces (figure 18D). The outer m prism faces are cov-
Sample 18 is the largest crystal, in the form of a ered by growth steps (figure 18E).
deep open cup (figure 18, A and B). Morphologically, Sample 19 is considered to be a half cup. Formally,
the columnar and somewhat distorted crystal shows the sample is described as a crystal formed of two
several prism faces and hexagonal dipyramids (see parts. The first part shows platy habit, with two basal
figure 3, C and D). The main opening at one end is in c faces and m, a, and i prism faces (figure 19A). On
Figure 19. A: Sample 19 (7.8 mm in length), an emerald crystal in the form of a half cup developed with two parts:
as a platy part with lower and upper basal pinacoid (white arrows) and an upper curved rim surrounding about
half of the area of the platy part; this rim is terminated by a small basal face (red arrow). B: Stepped surface of the
basal face on top of the horizontal surface of the rim. C: View of the inner surface of the circular rim on top of the
platy part, in this orientation with reflective steep k hexagonal dipyramids, the elongated cavities are filled with
fine-grained white beryl. Photos by G. Martayan (A) and K. Schmetzer (B and C); field of view 14.5 mm (B).
A B C
k
rim rim
rim
rim
beryl
platy
platy
platy platy
3.5 mm in diameter. The diameter of the channel The rims or walls end with faces oriented perpen-
through the crystal at the other end is approximately dicular to the c-axis, and the outer surface of the
1.0 mm. Outside, the tube is terminated by m prism rims are formed by various prismatic and pyramidal
faces, which show etch features—i.e., the original sur- faces. The inner surface of the walls or rims are
face of the tube is partially dissolved (figure 22). The formed by the same faces, mainly first- and second-
horizontal part of the wall or rim oriented parallel to order prism faces and occasionally in combination
the basal pinacoid (see figure 21B) reveals small pits, with steep dipyramids. This means that the outer
most likely due to etching. and the inner outlines of the skeletal beryl walls are
Evaluation. Samples 11–21, all originating from parallel to prismatic and steep dipyramidal faces.
Chivor, show the same phenomenon: incomplete Within these depressions or cavities, we observe ir-
growth of the basal face, but with a different degree regular walls or columns, which end at different
of development. In general, our Colombian samples heights in the cavities with small basal faces. In
display an upper rim surrounding indentations (see samples 15 and 16, it is clearly indicated that the
again figures 12 and 13) and somewhat deeper depres- inner bottom of the cavities is confined to a zone of
sions (figures 14 and 15) or somewhat higher walls or strong color zoning, which indicates a change of
rims surrounding deeper cavities (figures 16–20). In growth conditions at this stage of crystal growth (see
other words: The patterns observed in cups of various again figures 15 and 16).
depths in samples 16–21 or in emeralds with deeper Considering the patterns described for beryl with
indentations of basal faces in samples 14 and 15 re- skeletal and polygonal growth (box B), we conclude
flect deeper indentation patterns on basal planes than that the morphology seen in Colombian emerald
those observed in samples 11–13. samples 11–19 can be understood as a combination
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chen Gesellschaft zu St. Petersburg, Zweite Serie, Vol. 31, pp. entific Translations Ltd., Jerusalem.
155–160. Gübelin E.J. (1944) Gemstone inclusions. G&G, Vol. 4, No. 12, pp.
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pp. 382–397 [in Russian]. Hainschwang T. (2008) Extraordinary “gota de aceite” emerald
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[Link]/gems-gemology
Pearl 1
Button
5.50 ct
Pearl 2
Drop
3.30 ct
Pearl 3
Oval
8.53 ct
Pearl 4
Button
5.87 ct
Figure 8. Surface appearance and internal structures of the four atypical bead cultured pearls. Fields of view 2 mm,
0.6 mm, 2.86 mm, and 16.3 mm.
the surface which was not continuous. center of the nucleus and a small “or- the culturing process (“Atypical
On viewing the μ-CT, the demarcation ganic tail-like feature” at one end ‘beading’ in the production of cul-
was more discernible and followed the within the boundary separating the tured pearls from Australian Pinctada
irregular outline of the pearl (figure 8, bead from the overgrown cultured maxima,” GIA Research News, Feb-
row 1). An irregularly shaped fresh- nacre (figure 8, row 3). All features ruary 13, 2017). This pearl exhibited
water shell bead was clearly used as the were consistent with a saltwater non- distinct surface scratches that were
nucleus, hence the strong yellowish bead cultured pearl being used as the visible without magnification.
green reaction observed in the optical bead nuclei. The lack of growth arcs Pearl 4 also showed a strong de-
X-ray fluorescence unit (figure 9, left). around the demarcation was possibly marcation feature on the RTX and μ-
Under transmitted light, banding due to rapid nacre deposition during CT images. However, the central area
within the bead nucleus was also ob-
served (figure 9, right); externally, the
pearl had notable indentations on its Figure 9. Left: Pearl 1 revealed a strong yellowish green reaction under
surface. optical X-ray fluorescence. Right: Undulating shell banding visible
Pearl 2 hosted the most interesting within the sample’s shell bead nucleus using transmitted light; field of
nucleus of the four. A rectangular “tis- view 6.75 mm.
sue-box” shaped bead, likely a piece of
cut saltwater shell given the almost
identical radio-opacity to that of its
host, was evident in the RTX and μ-
CT images (figure 8, row 2) (Fall 2022
Gem News International, pp. 378–
380). Externally, the pearl was
smooth, lustrous, and free of any sur-
face blemishes.
The RTX and μ-CT images of
pearl 3 revealed an obvious demar-
cation with a linear structure at the
7 8 9 10 11 12
Figure 10. A group of 12 pearls ranging from 7.38 × 6.49 × 6.05 mm to 10.61 × 9.05 × 8.05 mm and weighing 44.37
carats total.
differed from the other three pearls, as color saltwater cultured pearls from weighing 44.37 carats total and rang-
it showed a void-like feature in the Pinctada maxima,” Fall 2012 G&G, ing in size from 7.38 × 6.49 × 6.05
middle (figure 8, row 4). The bead nu- pp. 193–197) and the pearls’ internal mm to 10.61 × 9.05 × 8.05 mm. The
cleus used in the process was most structures and external appearance (A. nine drilled pearls appeared to be old,
likely a saltwater non-bead cultured Homkrajae et al., “Internal structures while the three undrilled pearls
pearl based on the fact that the pearl of known Pinctada maxima pearls: looked whiter and much newer over-
was inert to XRF, in keeping with Cultured pearls from operated marine all (figure 10). The shape of the sam-
pearl 3, despite the relatively thin mollusks,” Fall 2021 G&G, pp. 186– ples varied, and the nine drilled pearls
nacre layers that would allow a fresh- 205), it is apparent that all four of possessed a notable “aged” yellow
water bead to react. The pearl was them formed within Pinctada species coloration, which was also evident on
also unusual because it possessed mollusks, most likely Pinctada max- some areas of the three undrilled
three nearly flat “bases” with concave ima. Atypical bead cultured pearls whiter pearls.
features at the center of each. This have always been an interesting and The older-looking pearls possessed
raised questions about its identity sometimes challenging subject. With a dull luster, but the nacre condition
even before X-ray examination, since modern equipment and practical pearl was good. Microscopic examination
the authors have rarely observed nat- testing experience, laboratories such at 70× magnification soon revealed
ural pearls with such features. as GIA aim to remain one step ahead that the color was concentrated on
This is not the first time GIA has of the possible experiments used by the outer layers and within surface-
encountered aBCPs, but to receive cultivators. reaching features, proving that the
four with variations on two types of Rajesh S. Patel, Abeer Al-Alawi, color was not natural and a treatment
nuclei—atypical shell (not typical Lubna Sahani, and Nicholas Sturman had been used to alter their appear-
round shell beads) and non-bead cul- ance (Summer 2017 Gem News Inter-
tured pearls—in one lot was very in- national, pp. 255–256).
teresting. This proves that such pearls Although the color of pearls can
Treated Freshwater Non-Bead
are still circulating in the market and change over time due to various
are being mixed with natural goods in Cultured Pearls with an Antique causes (e.g., care factors such as stor-
an attempt at deception (Fall 2011 Lab Appearance age conditions and contact with
Notes, pp. 229–230). Given the spec- GIA’s Mumbai laboratory recently re- chemicals), these changes tend to be
tral data collected (S. Karampelas, ceived for identification a group of very gradual and develop over many
“Spectral characteristics of natural- nine drilled and three undrilled pearls years. This is partly due to their bio-
Real-time microradiography (RTX), The ultraviolet/visible reflectance G&G, pp. 202–215). When the surface
shown in the top row of figure 18, re- spectra showed a prominent feature at structures were compared to photo-
vealed a pleasant surprise. An obvious around 450 nm and weaker features at micrographs of known Pinna species
and intriguing gastropod shell was 320, 330, 450, and 460 nm proving shell from GIA’s Bangkok laboratory
hidden beneath the overlying layers, that the sample’s color was natural (figure 17, C and D), the results showed
which resulted in further study using and lacked any treatment. Raman some similarity. However, Raman
X-ray computed microtomography (μ- analysis using 514 nm laser excitation spectra indicative of calcite were ob-
CT) (figure 18, bottom row). The mi- showed a series of peaks at 158, 186, tained for the Bangkok research collec-
nute details of a unique marine 204, and 213 cm–1; a weak peak at 280 tion samples, which differed from the
gastropod exoskeleton measuring ap- cm–1; a doublet peak around 701–704 sample studied here. The Atrina vex-
proximately 8.30 × 5.75 mm were ob- cm–1; and a strong peak at 1085 cm–1. illum species may have been respon-
served within a void feature, and the These were indicative of aragonite. sible for producing the natural shell
overlying growth layers on the face The photoluminescence spectra were blister, and this would explain the
side (the surface that grew within the also consistent with the Raman and aragonite-related Raman peaks since
mollusk it formed in) revealed mini- displayed high fluorescence and arag- this mollusk is known to produce
mal growth arcs. Marine gastropods onite-related peaks. These results pearls with an aragonitic structure.
are known to vary in size, and the were unexpected given the cellular- However, since Atrina species pearls
class consists of many thousands of looking structure observed through are often nacreous when aragonite is
species (A. Nutzel., “Larval ecology the microscope, as this type of struc- present and the sample in question
and morphology in fossil gastropods,” ture usually results in Raman spectra was non-nacreous, the contradicting
Paleontology, Vol. 57, No. 3, 2014, pp. indicative of calcite. data still leaves some doubt as to the
479–503). These observations pro- While the lustrous dark color and true identity of the host. Nevertheless,
vided enough evidence to make a the cellular-looking structure indi- this example of a shell blister encom-
clear distinction between a shell cated the host shell was likely a passing a gastropod shell represents a
blister, such as this sample, and a species from the Pinnidae family, it noteworthy phenomenon of nature
shell blister pearl (“Natural shell was not clear given the spectral data that is rarely encountered.
blisters and blister pearls: What’s the collected (N. Sturman et al., “Observa-
difference?” GIA Research News, Au- tions on pearls reportedly from the Jayesh Surve, Abeer Al-Alawi, and
gust 26, 2019). Pinnidae family (pen pearls),” Fall 2014 Nicholas Sturman
RUBY with Interesting Synthetic gonally shaped, platy crystals (Fall using polarized light, but careful anal-
Overgrowth 2002 G&G Lab Notes, pp. 255–256). ysis is required because the over-
The Carlsbad laboratory received a When viewed in reflective lighting, growth can completely fill cavities
3.02 ct ruby for a colored stone iden- there is no luster difference between and be inconspicuous.
tification and origin report. Standard the host corundum and the synthetic
overgrowth, as the two materials have Nicole Ahline
gemological testing was consistent
with ruby: a hydrostatic specific the same refractive index. The gaps
gravity of 3.96 and a ruby spectrum that could be observed between the
crystals in this stone showed how Exceptionally Large
in a handheld spectroscope. Inter-
they grew in different orientations. SYNTHETIC RUTILE
nally, the stone displayed white
flakes in a hexagonal formation and Synthetic overgrowth is common The Carlsbad laboratory received three
roiled graining. Partially healed fis- enough that it should always be light yellow modified round brilliants
sures with residue, which result looked for in corundum that has un- weighing 11.13, 11.91, and 110.18 ct
from heating in the presence of a dergone high-temperature heat treat- (figure 20) for identification reports.
flux, were also documented. The in- ment. There are cases where Standard gemological testing revealed
clusion scene, along with the stone’s synthetic overgrowth can be observed the stones to be synthetic rutile based
trace element chemistry collected
using laser ablation–inductively
coupled plasma–mass spectrometry
(LA-ICP-MS), were consistent with Figure 20. Three large synthetic rutile brilliants weighing 11.13, 110.18,
Burmese ruby. This ruby was not and 11.91 ct. Courtesy of Arya Akhavan.
treated by beryllium diffusion, as no
beryllium was detected by LA-ICP-
MS. The curious feature of this
stone was a large cavity on the pa-
vilion that was partially filled with
synthetic overgrowth that was ob-
served in the microscope (figure 19).
Synthetic overgrowth can be a by-
product of heating a piece of corun-
dum at high temperatures, with or
without the presence of a flux. This
creates an environment in the crucible
that allows for the partial dissolution
of corundum and can result in syn-
thetic corundum overgrowth on the
surface and in cavities of the heated
stone. Synthetic overgrowth is typi-
cally an aggregated structure of hexa-
Second Place
GEMS ON CANVAS: PIGMENTS HISTORICALLY SOURCED FROM GEM MATERIALS
FALL 2022
Britni LeCroy
Britni LeCroy is a staff gemologist at GIA in Carlsbad, California. She obtained a bachelor’s
degree in geoscience from the University of Texas at Dallas before receiving gemology diplomas
from GIA and the Gemological Association of Great Britain. A frequent contributor to G&G, her
areas of interest include pearls, organic gem materials, and historical gemology.
Britni LeCroy
Third Place
A CANARY IN THE RUBY MINE: LOW-TEMPERATURE HEAT TREATMENT EXPERIMENTS ON
BURMESE RUBY
WINTER 2022
E. Billie Hughes and Wim Vertriest
E. Billie Hughes is a gemologist and cofounder of Lotus Gemology in Bangkok. An award-winning
photomicrographer and sought-after lecturer, she has delivered talks on gemology around the
world. She is a graduate of the University of California, Los Angeles. Wim Vertriest is manager of
E. Billie Hughes Wim Vertriest
field gemology at GIA in Bangkok, where he curates GIA’s colored stone reference collection. He
obtained a master’s degree in geology (geodynamics and geofluids) from KU Leuven in Belgium.
Many thanks to the members of G&G’s Editorial Review Board for voting this year.
About the banner: Acicular inclusions of the blue mineral dumortierite are
present throughout this quartz crystal from Brazil. Photomicrograph by
Nathan Renfro; field of view 5.68 mm.
crystals present, the overall appearance of this alexandrite’s reaction. After exposure to sunlight or artificial light with
multiphase inclusion is comparable to the typical jagged a UV component, samples can quickly develop a much
three-phase inclusions that are distinctive for Colombian stronger color. One hackmanite sample recently examined
emerald. by the author (figure 3) showed this phenomenon.
Jamie Price Another hackmanite was submitted that displayed an
GIA, Carlsbad interesting elongated white inclusion (figure 4, left) that was
identified by micro-Raman as apatite. As we examined the
sample in the microscope, we tried exposing it to a 6-watt
Apatite in Hackmanite long-wave UV light for approximately one second. Almost
Hackmanite, Na8Al6Si6O24(Cl2,S), is a variety of sodalite no- immediately, a change was observed. The hackmanite de-
table for its tenebrescence. When kept in darkness, samples veloped a more vibrant purple color that is clearly displayed
can fade to pale purple and even gray or translucent to in figure 4 (right).
opaque white. When exposed to long-wave ultraviolet il- E. Billie Hughes
lumination, they can display a strong orange fluorescence Lotus Gemology, Bangkok
Figure 4. Left: In darkfield illumination, a white apatite crystal is visible in the hackmanite. Right: After expo-
sure to long-wave UV light for approximately one second, a dramatic change can be seen. The overall color of the
hackmanite is now a more vivid shade of purple. Photomicrographs by E. Billie Hughes; field of view approx-
imately 5 mm.
Figure 8. This partially exposed orange garnet inclusion with surrounding fractures in a brownish yellow diamond
resembled a flying insect. Photomicrograph by Mei Yan Lai; field of view 1.58 mm.
cubic crystal system, and these can be forced into other tern (figure 12). Careful examination revealed a partially
diamond habits. For example, a monoclinic crystal of di- healed fissure intersecting one of the negative crystals, in-
opside may be forced into a cuboctahedral habit. Xeno- dicating the stone had been subjected to heat treatment.
morphic crystals are just one of many unique inclusion Fortunately, this spectacular pattern of negative crys-
types possible within diamond. tals endured the heat treatment process, decorating the in-
Britni LeCroy and Virginia Schwartz ternal micro-world of this sapphire.
GIA, Carlsbad Piradee Siritheerakul and Tao Shiu Hei
GIA, Bangkok
1.768, a chromium emission line in red using a handheld temperature, pressure, and chemistry. While some of these
spectroscope, medium red fluorescence under long-wave growth details are submicroscopic and remain hidden dur-
UV, and weak red fluorescence under short-wave UV. ing microscopic observation, other features such as min-
These properties were consistent with ruby. Microscopic eral inclusions and encapsulated fluids are waiting to be
examination using brightfield illumination revealed nu- discovered. In a very real sense, inclusions and their devel-
merous dark red inclusions (figure 13) that resembled crys- opmental sequencing in their host gems and minerals are
tals commonly seen within natural corundum. descriptions of mineralogical genetics.
Furthermore, magnification showed characteristic in- Researchers focused specifically on inclusions usually
ternal features of flame-fusion ruby such as curved striae cannot outbid serious gem and mineral collectors for crys-
and gas bubbles. The strong curved growth lines and nu- tals and fashioned gems with interesting internal targets.
merous gas bubbles (figure 14) suggested that this was an As a result, many such “gems” end up in private collec-
early type of flame-fusion ruby. Although flame-fusion co- tions, and their inclusions are rarely, if ever, fully doc-
rundum is widely available in the marketplace, it is un- umented. This is a tremendous missed opportunity,
usual to encounter a specimen containing natural-looking because inclusions contain geological information that
dark red solid inclusions. These inclusions are possibly un- tells a story about themselves and their host.
melted alumina powder, and the fact that Raman was un- For this issue’s Quarterly Crystal, we recently had the
able to identify something other than alumina supports opportunity to document a well-formed gem-quality, trans-
this (E.J. Gübelin and J.I. Koivula, Photoatlas of Inclusions parent, very light greenish blue terminated hexagonal crys-
in Gemstones, Volume 3, Opinio Publishers, Basel, Switz- tal of aquamarine, with a small amount of light brown
erland, 2008). matrix at the base and a clearly visible inclusion cluster at
Identification of the natural or laboratory-grown origin the near center (figure 15). The aquamarine was obtained
of a stone with this type of natural-looking inclusion can from Muntazir Mehdi of Shad Fine Minerals International
be difficult. Careful observation is needed to correctly iden- in Gilgit-Baltistan, Pakistan. The geographic source was re-
tify such a specimen’s origin. portedly the Kharguluk mine in Baltistan Province.
Ezgi Kiyak At 56.00 ct with corresponding measurements of 26.36
GIA, New York × 16.09 × 15.02 mm, this aquamarine played host to an
easily eye-visible tight cluster of randomly arranged dark
reddish brown to black bladed crystals (figure 16) that re-
Quarterly Crystal: Columbite(?) in Beryl sembled the mineral columbite-(Mn), Mn2+Nb2O6 , as
Those in the gem and mineral community can appreciate shown by E.J. Gübelin and J.I. Koivula (Photoatlas of Inclu-
the near-perfection of a beautifully crystallized mineral sions in Gemstones, Volume 2, Opinio Verlag, Basel, Switz-
specimen or a well-cut gemstone. But these surfaces are erland, 2005, pp. 263, 319).
only the exterior, covering a complex, multilayered story Micro-Raman has significantly reduced the time re-
within. These internal contents often remain unknown quired to instrumentally identify many inclusions. Some
unless we choose to explore below the surface. Somewhat inclusion identifications that once took hours can now be
like trees and their rings, minerals and gems form as con- made in a matter of minutes using this technique. The
centric, typically crystallized layers, recording the devel- Raman instrument can also analyze some subsurface in-
opmental details within each layer through changes in clusions at depths of more than a millimeter in certain fa-
vorable instances, which means inclusions do not need to stone. Due to the value of this inclusion specimen, we
be exposed to the surface. opted to forgo destructive analysis and keep the beryl crys-
After several Raman attempts from different directions, tal intact for future gemological exploration.
we realized that destructive analysis would be needed to John I. Koivula and Nathan Renfro
clearly identify the inclusion cluster deep within this GIA, Carlsbad
1. Nearly half of the diamonds from C. is reliant upon carbon dating. C. has high levels of trace impurities.
Guyana D. is not currently possible. D. rivals Imperial topaz in color.
A. have green spotting or skins.
B. are found as aggregates. 4. Only the most important paintings [Link] higher the silica content detected
C. reach 10 carats in size. were allowed to use this natural in turquoise, the more likely
D. possess D color. pigment during its prime. A. it will command a higher per-carat
A. Ultramarine price.
2. Heating ruby to 600°C may B. Red ochre B. it will have a higher specific gravity.
A. significantly alter the Raman spectra C. Cinnabar C. its bodycolor will be sky blue.
of any spinel inclusions. D. Azurite D. it has been porcelain treated.
B. cause fissures to begin forming
around solid inclusions. 5. Amber from Phu Quoc, Vietnam 8. Chinese sapphire from Muling
C. affect sphene and apatite inclusions A. is mostly opaque. A. is mostly yellow, green, and blue in
the most. B. is almost exclusively pale yellow in color.
D. alter the appearance of any mica color. B. is always heavily weathered in its
inclusions. C. commonly contains fauna. rough form.
D. commonly contains gas bubbles C. shows remarkable optical homo-
3. Geographic origin determination of and spangles. geneity.
diamonds D. can be blue and yellow bicolor.
A. is reliant upon identification of 6. Schneckenstein topaz
inclusions. A. is currently an important commer- 9. Today, the Habachtal emerald mine
B. is reliant upon trace element cial gemstone. A. produces emeralds similar to those
analysis. B. likely formed at low temperatures. from Colombia.
A familiar wire paper clip can serve to demonstrate de- in the kitchen. Although we cannot feel and observe dia-
formation. If you bend it just slightly, it will deform elas- mond deformation in the same way, it involves the same
tically and return to its unbent shape. The elastic behavior basic principles at the atomic scale. During plastic defor-
is what allows a paper clip to hold on to a few sheets of mation, atomic bonds are breaking and re-forming along
paper. If you bend it beyond a certain point, the bend be- imperfections called dislocations. Plastic deformation in
comes permanent. This is plastic deformation. If you bend all crystalline solids, including diamond, is accomplished
it back and forth a few times in one spot, the paper clip will by the creation and movement of dislocations (Nesse,
break. 2017).
Often we see just one of these three mechanisms dom- A dislocation is a linear (one-dimensional) disruption in
inate, whether it is elastic, brittle, or plastic. Deformation the regular, repeating atomic structure. Figure 2 shows a
behavior depends on many factors, such as the tempera- simplified illustration of a dislocation in a crystal lattice.
ture, how much stress is applied, and, of course, what kind The dislocation is shown end-on, and the crystal lattice ap-
of material it is. For diamond, temperature is a key factor. pears to have an extra half-plane of atoms, shown in orange
If you tried to squeeze, twist, or stretch a diamond at room (figure 2), which resembles a half sheet of paper inserted
temperature, the elastic deformation would be minimal. It into an otherwise orderly paper stack. This is an edge dis-
is among the most rigid of all known materials. If it is sub- location, one of two major dislocation types. The second
jected to high stresses, diamond tends to exhibit brittle de- type is a screw dislocation, which has a different geometry.
formation by cracking or chipping. But at higher Dislocations allow a crystal to deform plastically little
temperatures, diamond begins to exhibit plastic deforma- by little as bonds break and re-form. The crystal as a whole
tion. Experiments show that significant plastic deforma- remains fully intact, as only a small number of its bonds
tion requires temperatures above approximately 900°C are broken at any given time. A dislocation is much like a
(DeVries, 1975; Weidner et al., 1994). wrinkle in a carpet (figure 2, bottom). A carpet could be
moved by introducing a wrinkle and working it across the
carpet. Most of the carpet remains in contact with the floor,
How Does Diamond Deform Plastically? but moving the wrinkle shifts the carpet slightly by break-
Many metal objects, including paper clips, deform plasti- ing and reestablishing contact with the floor. Similarly, as
cally under conditions we can easily create and deform to dislocations move through a crystal, they can allow atomic
a degree that is obvious. Our understanding of how crys- layers to move with respect to one another. Systematic
talline solids deform is underpinned by engineering studies movement of many dislocations can allow the whole crys-
of metals, such as steel used for car frames and bridges. tal to deform plastically when subjected to stress.
Aluminum foil is an example of a metal whose plastic de- Given that crystals are orderly structures, it should
formation behavior can be felt as we shape and conform it come as no surprise that dislocation movement is not ran-
Polarizing filters are a simple yet powerful tool for this ap- pattern of anomalous birefringence, such as banding, mot-
plication, whether using a polariscope or a gem microscope tling, or cross-hatching.
(Renfro, 2015). Viewing a diamond using crossed polarizing Plastic deformation can also be observed using cathodo-
filters is an easy way to see anomalous birefringence, luminescence imaging or deep UV fluorescence imaging
which in natural diamond is typically the result of plastic (e.g., DiamondView). These techniques are especially use-
deformation (figure 5). With this technique, a perfect, un- ful for examining polished diamond surfaces, where slip
strained diamond should appear uniformly dark inside. planes can appear as bright or dark lines (figure 6, left). An-
Bending and twisting of the light as it passes through de- other deformation-related pattern sometimes revealed
formed (strained) regions of the diamond will result in a with these methods is dislocation networks (figure 6,
Figure 5. A natural type IIa diamond with evidence of plastic deformation. Examination with a microscope using
crossed polarizing filters (left) reveals internal banding of dark/light and interference colors due to strain-related
anomalous birefringence. In this diamond, the geometry of the banding correlates with the appearance of unusual
whitish graining (right). The hazy whitish graining may be caused by plastic deformation. Photomicrographs by
Evan M. Smith; field of view 4.79 mm.
right), which have a cellular appearance resembling mud multiple dislocations interact or jogged dislocations move
cracks or a fine mesh (De Corte et al., 2006). Dislocation through the crystal (Leipner et al., 2000, 2003). At the high
networks are thought to be the result of not just plastic de- temperatures necessary for plastic behavior, these vacan-
formation, but also a period of recovery at high tempera- cies are mobile and tend to cluster into groups. These small
tures that allows the dislocations to reorganize into a more groups of vacancies can absorb visible light and cause color.
stable configuration (Hanley et al., 1977). This process may Vacancy clusters made up of about 40−60 vacancies are
be similar to hammering or working metals and then heat- thought to be responsible for the common brown color in
ing them up to relax and reconfigure the tangled disloca- diamond (Avalos and Dannefaer, 2003; Hounsome et al.,
tions that have been introduced. Sublithospheric or 2006; Barnes et al., 2007).
superdeep diamonds often have dislocation network pat- The cause of deformation-related pink is believed to be
terns, and it has been suggested that their formation is pro- similar but involves a broad absorption band centered near
moted by low nitrogen content and/or high temperatures 550 nm that is not fully understood (Gaillou et al., 2010). To
(Smith et al., 2019). be fair, not all brown and pink color is attributable to plastic
deformation, but it is the leading cause (Harris et al., 1979;
Fisher, 2009). An excellent review of brown and pink color
How Does Plastic Deformation Cause Color? in diamond was presented in Eaton-Magaña et al. (2018).
In 1999, General Electric and Lazare Kaplan International
announced that HPHT processing could be applied as a com-
mercial treatment to decolorize brown diamonds (Vagarali What Causes the Deformation?
et al., 2004). This spurred research into the cause of brown It is plain to see that many natural diamonds bear evi-
color, which up until that point had been poorly understood. dence of plastic deformation, but it is not intuitively ob-
Visual indications of deformation had long been recognized vious why this should be the case. There must be some
to correlate with the presence of brown and to a lesser extent geological processes that lead to compression or shearing
pink colors in diamond (Urusovskaya and Orlov, 1964; Har- forces that occasionally deform diamonds. The geological
ris et al., 1979). Internally, these colors often concentrate process should be neither too gentle, because the relatively
along slip planes, glide planes, or less distinctly along “grain- soft silicate host rocks should simply flow around the di-
ing,” all of which are deformation features. Theoretical amonds, nor too violent, which would break diamonds
modeling and experiments played important roles in linking rather than plastically deform them. Several theories have
brown color to dislocation movement and the creation of been proposed.
vacancies in the crystal structure (Avalos and Dannefaer, Kimberlites and related eruptions that bring diamonds
2003; Hounsome et al., 2006; Barnes et al., 2007). from the mantle up to the surface could have the power to
A vacancy is a missing atom in the crystal lattice. Va- deform diamonds. The magmatic journey is thought to be
cancies can be created during plastic deformation when relatively violent, however, and it is clear that diamonds
ACKNOWLEDGMENT
Many thanks to Dr. Steven B. Shirey for discussion and suggestions that helped to improve this column.
REFERENCES
Avalos V., Dannefaer S. (2003) Vacancy-type defects in brown dia- Willems B. (2006) Overview of dislocation networks in natural
monds investigated by positron annihilation. Physica B: Con- type IIa diamonds. G&G, Vol. 42, No. 3, pp. 122–123.
densed Matter, Vol. 340-342, pp. 76–79, DeVries R.C. (1975) Plastic deformation and “work-hardening” of
[Link] diamond. Materials Research Bulletin, Vol. 10, No. 11, pp.
Barnes R., Bangert U., Scott A. (2007) Investigating large vacancy 1193–1199, [Link]
clusters in type IIa diamond with electron energy loss spec- Dobrinets I.A., Vins V.G., Zaitsev A.M. (2013) HPHT-Treated Dia-
troscopy (EELS). Physica Status Solidi (a), Vol. 204, No. 9, pp. monds: Diamonds Forever. Springer Series in Materials Science,
3065–3071, [Link] Springer Berlin, Heidelberg, [Link]
Bulanova G.P., Speich L., Smith C.B., Gaillou E., Kohn S.C., Wib- 642-37490-6
berley E., Chapman J.G., Howell D., Davy A.T. (2018) The Eaton-Magaña S., Ardon T., Smit K.V., Breeding C.M., Shigley J.E.
unique nature of Argyle fancy diamonds: Internal structure, (2018) Natural-color pink, purple, red, and brown diamonds:
paragenesis, and reasons for color. In A.T. Davy et al., Eds., Band of many colors. G&G, Vol. 54, No. 4, pp. 352–377,
Geoscience and Exploration of the Argyle, Bunder, Diavik, [Link]
and Murowa Diamond Deposits, Volume 20. Society of Eco- Evans T., Wild R.K. (1965) Plastic bending of diamond plates. Philo-
nomic Geologists, Littleton, Colorado, pp. 169–190, sophical Magazine: A Journal of Theoretical Experimental and
[Link] Applied Physics, Vol. 12, No. 117, pp. 479–489,
Condie K.C., Pease V., Eds. (2008) When Did Plate Tectonics Begin [Link]
on Planet Earth? Geological Society of America, Special Paper Fisher D. (2009) Brown diamonds and high pressure high tempera-
440, 294 pp. ture treatment. Lithos, Vol. 112, pp. 619–624,
De Corte K., Anthonis A., Van Royen J., Blanchaert M., Barjon J., [Link]
For online access to all issues of GEMS & GEMOLOGY from 1934 to the present, visit:
[Link]/gems-gemology
These seminars are avocational and are not intended to prepare individuals for entry-level [Link] are non-credit bearing and do not lead to a GIA academic credential.
They do not fall under the approval of the Accrediting Commission of Career Schools and Colleges (ACCSC) or the Distance Education Accrediting Commission (DEAC).
© 2023 Gemological Institute of America, Inc. All trademarks owned by Gemological Institute of America, Inc. and used under license.
GEM NEWS INTERNATIONAL
Contributing Editors
Gagan Choudhary, IIGJ-Research & Laboratories Centre, Jaipur, India ([Link]@[Link])
Christopher M. Breeding, GIA, Carlsbad ([Link]@[Link])
Guanghai Shi, School of Gemmology, China University of Geosciences, Beijing (shigh@[Link])
in figure 3. Tourmaline from newly discovered pockets in The demand for one-of-a-kind gems was apparent in all
San Diego County’s Pala District was also on display. aspects—cut, color, and even inclusions. Nontraditional
cuts such as slices, fantasy cuts, rose cuts, kites, and tablets
were readily found in gems ranging from rutilated quartz
Figure 3. This pin features a 63.92 ct Ethiopian opal to diamond (figure 4). Beyond nonstandard cuts, stones
with 23.85 carats of conch pearl, 5.88 carats of natural
pearl, and 15.85 carats of diamond, set in platinum.
Photo by Robert Weldon; courtesy of Pioneer Gems of Figure 4. Earrings featuring diamond slices and rose-
New York. cut rubies. Photo by Mimi Travis.
Figure 6. An unusual 6.95 ct cushion-cut bicolor alexandrite from Madagascar displaying a color change from yel-
lowish green and reddish brown in daylight (left) to yellowish orange and orangy brown in incandescent illumina-
tion (right). Photos by Robert Weldon; courtesy of Bryan Lichtenstein, 3090 Gems, LLC.
before it was finally cut in 2017 by Rohitha Perera in Sri 9). Processed and brought to market as tumble-polished
Lanka (figure 8, right). The Bowersoxes have several other freeforms, the chalcedony was offered by Orbit Ethiopia Plc.
cut gems from this find, with the next largest weighing in According to managing director Tewodros Sintayehu, the
at 541.96 ct. mine is located in the Gamo Zone region, approximately
Jennifer Stone-Sundberg and Si Athena Chen 600 km from Addis Ababa. The material was first discov-
GIA, Carlsbad ered in the Gerese District and has since been found in the
adjacent districts of Kamba and Garda Marta. Sintayehu
noted that he had a very large quantity of the material
New violet orbicular chalcedony from Ethiopia. At the GJX stockpiled.
show, the author encountered a relatively new find of violet The notable features of this material were its fairly vivid
chalcedony reportedly discovered in Ethiopia in 2019 (figure violet color as well as the multitude of white orbicular struc-
tures distributed across the surface of the gems (figure 10). tions for harvesting coral are in place today. Harvesting is
Microscopic examination revealed that the white color was limited to coral with trunks having a basal diameter of at
related to a distinct botryoidal structure where a shallow least 7 mm recovered from 50 meters or deeper by licensed
outer layer of the gems contained all of the white areas. Be- scuba divers.
cause the white orbs are confined to a shallow surface layer, Precious coral is the exoskeleton of very tiny marine
this explains why the material was sold as tumble-polished invertebrates, known as coral polyps. When a colony of
nuggets: Cutting the material into cabochons would likely polyps arrives in a particular area, they start to create the
result in the loss of the white orbicular pattern. A few exoskeletons on rocks, growing upward in a branch-like or
unidentified mineral inclusions were also observed with the fan formation. Di Gennaro mentioned that divers do not
microscope, but the cause of the outer layer’s white orb pat- harvest coral with active colonies as these will continue
tern remains unclear. to grow and the future, larger coral will be more valuable.
This new material is quite remarkable for its beautiful Divers therefore tend to harvest the coral where the colony
pattern. Even if it is only made available as freeform tumble- has already left. Unlike other types of corals, such as com-
polished stones, it will be a welcome addition to the chal- mon and reef, these Mediterranean “deep sea” precious
cedony market. corals are not a natural habitat for other marine species.
Nathan Renfro Reef coral species, which are a natural environment to
GIA, Carlsbad many different marine species, are in many cases endan-
gered and must be preserved.
Italian precious coral. Coral from the Mediterranean Sea Di Gennaro explained that the quality of the coral de-
has been harvested and used for adornments for thousands pends on the locality. He showed us a piece of dark red
of years. More than 7,000 species are categorized as pre- coral (figure 11, left), which is the typical color of coral har-
cious, common, or reef coral. Precious coral is defined by vested from northern Sardinia. It is a darker red due to
the World Jewellery Confederation (CIBJO) Coral Commis- cooler water temperatures from strong currents in the area.
sion as “those that are used in jewelry and decoration, Coral from the southern portion of Sardinia (figure 11, cen-
specifically red, pink, and white varieties with porcelain- ter) tends to be lighter in color. Di Gennaro described this
like luster after polishing.” Italian coral harvested from the as a more “classic” color of Mediterranean coral. He also
Corallium rubrum species is considered precious. showed us a piece of reddish orange coral called “Sciacca,”
At the GJX show, the authors spoke with Sergio Di named for a town in southern Sicily where the coral is har-
Gennaro of Fulvio Di Gennaro Srl. (Torre del Greco, vested (figure 11, right). Di Gennaro said that volcanic ac-
Naples) about the Italian coral market. The Mediterranean tivity below the surface results in warmer water
has been precious coral’s major source since it was first col- temperatures, which in turn causes a more orangy color.
lected for ornamentation over 3,000 years ago, followed by Di Gennaro emphasized the importance of sustainability
Taiwan and Japan with smaller quantities. Beginning in the in the coral industry, noting the heritage of the city of Torre
late 1970s, Mediterranean coral was threatened by over- del Greco, which was built on the art of processing coral.
harvesting. Di Gennaro explained that many strict regula- While current restrictions have reduced the amount of coral
being harvested compared to decades past, sustainable pro- change like this one is extraordinary,” he said. “A size of 35
duction will guarantee that we continue to see stunning carats is what makes it outstanding.”
Mediterranean precious coral for decades to come.
Lisa Kennedy and Cristiano Brigida
Figure 12. A 155 g aquamarine crystal containing a liq-
GIA, New York
uid and gas bubble inclusion. The crystal measures
11.9 cm long and the inclusion 4.3 cm long. Photo by
Exceptional gemstone acquisitions by the Kreis family. Robert Weldon; courtesy of Kreis Jewellery GmbH.
Kreis Jewellery (Niederwörresbach, Germany) is known for
master cutting expertise and distinctive jewelry design (see
Spring 2022 GNI, pp. 86–87). At the GJX show, Stefan and
Alexander Kreis showed us three recent gemstone acquisi-
tions.
First was a 155 g aquamarine crystal containing a two-
phase liquid and gas inclusion measuring 4.3 cm long (figure
12; see video at [Link]/gems-gemology/spring-2023-
gemnews-kreis-family-gemstones). The crystal was found
in the 1960s in Marambaia, Minas Gerais, Brazil, and had
been part of a private collection before the Kreises obtained
it in 2022.
“It would even be a cuttable crystal,” Alexander said.
“Of course we would never touch it because of the spe-
cialty of the huge liquid inclusion. A liquid chamber that
size in quartz would already be amazing,” he continued.
“But having it in an aquamarine, which is totally intact—
you have the complete termination. And look at the sheer
size of that crystal.”
Marambaia was known for large quantities of aquama-
rine by 1900 and produced the 110.5 kg (244 lb), 552,500 ct
Papamel, discovered in 1910, the largest known gem-quality
aquamarine crystal. The crystal that was the basis for the
Dom Pedro, the largest cut aquamarine, weighed around 45
kg (100 lb) and was also from Marambaia.
Stefan said they had received a 35.05 ct cat’s-eye alexan-
drite (figure 13) that morning. He noted the size, exception-
ally sharp eye, and superb color change for Sri Lankan
alexandrite, which typically has a weaker color change than
material from Russia and Brazil. Alexander pointed out that
cat’s-eyes are less common in alexandrite than in other
chrysoberyl. “A cat’s-eye alexandrite with a strong color
The Kreises also showed us a 7.08 ct padparadscha sap- exclusively in White Cliffs and typically occur within
phire (figure 14). “The color mixture of this stone is a real weathering-bleached siltstones and claystones. According
padparadscha color,” Stefan said. Alexander added that a to Dowton, no other type of gem-quality opal was found
range of colors fall into the padparadscha category, but in the same layer where the pineapple opals were mined.
“this is the perfect color.” During mining, it was noticed that two opals had formed
The cat’s-eye alexandrite and padparadscha sapphire will within a few feet of each other but with distinctly different
undoubtedly inspire exquisite jewelry designs from Sonja coloration: One displayed a rich spectrum of play-of-color,
and Vanessa Kreis. Sonja noted, “It is a very intuitive process while the other showed almost no coloration. The 3,510
in which we try to bring out a gem’s natural beauty in such ct Heart of Australia (figure 15) shows rich play-of-color
a way that it blurs the boundaries between jewelry and art.” and is considered one of the finest specimens of this type
Erin Hogarth ever unearthed. In some of Dowton’s samples, the precur-
GIA, Carlsbad sor calcite was not fully substituted by silica gel, and
white calcite crystals can be observed (figure 16).
Ikaite, CaCO3·6H2O, is a rare and metastable hydrated
Rare double pseudomorph ikaite-calcite-opal. At the
carbonate in sedimentary rocks that has only been identified
Pueblo Gem & Mineral Show, Graeme Dowton of Red
in environments ranging from –2° to 7°C in nature (M.L.
Earth Opal (White Cliffs, Australia) exhibited rare double
Vickers et al., “The ikaite to calcite transformation: Impli-
pseudomorph ikaite-calcite-opal gem specimens mined
cations for paleoclimate studies,” Geochimica et Cos-
from the Naatji Nest mine at White Cliffs in New South
mochimica Acta, Vol. 334, 2022, pp. 201–216). The
Wales, Australia. Ikaite was initially substituted with cal-
occurrence of ikaite suggests a period of very cold to near-
cite and then opalized, therefore making these double
freezing paleoclimate conditions in White Cliffs. At ambient
pseudomorph opals. Also called “pineapple opal” in the
market due to the form of their clusters, they are found
Figure 15. The Heart of Australia, a 3,510 ct double
pseudomorph ikaite-calcite-opal gem specimen, is
Figure 14. A 7.08 ct padparadscha sapphire. Photo by considered one of the finest ever unearthed. Courtesy
Robert Weldon; courtesy of Kreis Jewellery GmbH. of Graeme Dowton.
that upon closer inspection, the freshwater pearls more tion of colors compared to traditional akoya BC pearls. Some
often show a rounded flat surface feature on an otherwise white, light cream, and cream pearls were also presented as
spherical pearl, a feature usually too small to affect basic unprocessed and untreated—steps normally used to improve
shape (figure 18). This feature is also occasionally observed appearance and alter color. However, many akoya BC pearls
in other types of freshwater cultured pearls. in the market have been processed to generate a classic
Eliko Pearl Company (New York City) displayed numer- white appearance. Vietnam has produced saltwater cultured
ous strands of Vietnamese akoya BC pearls with bodycolors pearls commercially since the 1990s and is expected to pro-
ranging from silver to light gray and light bluish gray with duce approximately 2,000 kg per annum (N. Sturman et al.,
exceptional orient (figure 19). These provide a greater selec- “Vietnam: Shell nuclei, pearl hatcheries, and pearl farming,”
Fall 2020 G&G, pp. 402–415), which is significantly smaller
than Japan’s anticipated annual production of approximately
Figure 19. Vietnamese akoya bead cultured pearls in 20 tons (roughly 18,000 kg) (T. Matsuyama et al., “Mass
various colors ranging from silver to light gray to light mortality of pearl oyster (Pinctada fucata (Gould)) in Japan
bluish gray. The pearls were said to be unprocessed in 2019 and 2020 is caused by an unidentified infectious
and untreated. Photo by Lisa Kennedy; courtesy of agent,” PeerJ, Vol. 9, 2021, article no. 12180).
Eliko Pearl Company. Eric Yen of Yen’s Jewelry & Accessories Inc. (San Fran-
cisco) and Alan Hakimian of Yoko London presented
strands that combined multicolor pearls from different
pearl types, offering variety and high fashion all at once (fig-
ures 20 and 21). Both pointed out that making mixed and
graduated color strands is an efficient use of all the pearls
produced from a harvest, just one example of economic
sustainability in the pearl industry. Producing only per-
fectly matched color stands would lead to more waste.
Overall, pearl dealers are looking forward to the return
of the gem, jewelry, and pearl shows in Hong Kong in 2023,
as these are some of the largest shows for cultured pearls.
Many have not been able to attend since 2019 due to lock-
down restrictions in Hong Kong.
Lisa Kennedy
Artitaya Homkrajae
GIA, Carlsbad
When comparing pearls from the two regions, Vock ex- sizes ranging from 5.65 to 12.33 mm in diameter. Quahog
plained, there are some differences. Basra pearls usually pearls are known for their unique range of colors, including
have a warmer bodycolor, while Australian pearls tend to white, beige, pink, lavender, purple, brown, and black. These
be whiter. Also, Basra pearls are often rounder than their 21 quahog pearls showed a wide color range, from white and
Australian counterparts. In fact, the Gulf region has the beige to deep purple and tan (figure 24, right). According to
highest percentage of round natural nacreous pearls of any Jeremy, lilac and deep purple are the most desirable and
producing area. He credited this to the smaller shell of the command the highest price. The color of a quahog pearl is
Gulf region mollusks. determined by various factors, including the clam species
To see Alex Vock explain these common appearances and environmental and geochemical conditions.
with examples from his current collection, go to Another rarity on display was a large (16.44 ct, 14.50 ×
[Link]/gems-gemology/spring-2023-gemnews- 14.36 × 11.95 mm) deep purple, button-shaped non-nacre-
natural-nacreous-pearls. ous pearl showing an obvious flame structure at its surface
Lisa Kennedy and Artitaya Homkrajae (figure 25). This pearl formed from one of the many
Spondylus species, also known as “thorny” or “spiny” oys-
ters, which are harvested on the western coast of the Amer-
Exceptionally rare pearls from ECIJA. At the GJX show,
icas as Spondylus princeps and Spondylus calcifer/limbatus.
ECIJA (Santa Barbara, California) displayed a variety of nat-
ural, wild, nacreous, and non-nacreous pearls, including
conch, oyster, scallop, abalone, and quahog pearls. Only
0.2% of all pearls in the current market are natural (S. Figure 25. This non-nacreous pearl weighing 16.44 ct
Karampelas et al., “Raman spectroscopy of natural and cul- and measuring 14.50 × 14.36 × 11.95 mm is reportedly
tured pearls and pearl producing mollusc shells,” Journal from a Spondylus calcifer/limbatus mollusk from the
of Raman Spectroscopy, Vol. 51, No. 9, 2019, pp. 1813– Sea of Cortez in Baja California. Photo by Robert
1821), and the authors found the non-nacreous collection Weldon; courtesy of ECIJA.
especially notable.
ECIJA owner Aylene Norris and her husband, Jeremy
Norris (Oasis Pearl), have been sourcing for 34 years and spe-
cialize in natural pearls. For the first time in Tucson, ECIJA
displayed a collection of round quahog pearls (figure 24).
Quahog pearls are produced in the bivalve mollusk Merce-
naria mercenaria (figure 24, left), a type of saltwater clam
native to the Atlantic Ocean. These non-nacreous pearls
consist mainly of fibrous aragonite and organic matter. They
are often not perfectly spherical but form irregular shapes
such as button or baroque, making this set of round quahog
pearls extremely rare (figure 24, right). Moreover, they ex-
hibited an attractive and strong porcelaneous surface with
Figure 26. These two quartz crystal scepters containing a multitude of complex petroleum fluid inclusions (left)
that fluoresce yellow to blue to long-wave UV light (right) are from a new deposit in Madagascar. The larger crys-
tal weighs 11.05 ct and measures 22.81 mm in length. Photos by Annie Haynes; courtesy of Hidden Gem Gallery.
Microscopic inclusions in quartz are enjoyable to ex- cut into cabochon form. However, transparent material has
amine, and petroleum inclusions are of particular interest always been found in this mine and makes up about 5–
to the collector due to their spectacular UV reaction. The 10% of the production.
introduction of this new quartz find at the Tucson show is At the AGTA show, Greenland Ruby displayed many
an exciting addition to the gem and mineral trade. examples of attractive transparent ruby and pink to orangy
Nathan Renfro and John I. Koivula pink sapphire, including several fancy-color sapphires in
GIA, Carlsbad sizes greater than one carat (figure 28; see also pp. 145–149
of this issue). These fancy colors are achieved by heat treat-
ing nearly colorless to slightly pink transparent material.
Bright orange sapphire from Greenland. The Aappaluttoq A transparent bright orange sapphire weighing 0.89 ct and
mine in Greenland is home to the oldest known ruby- measuring 6.41 × 5.02 mm (figure 29) immediately caught
bearing rocks on Earth. These host rocks are nearly three our eye. Martin Viala, product manager for Greenland
billion years old (A. Polat et al., “New age (ca. 2970 Ma), Ruby, shared with us a video of the original 1.07 g sapphire
mantle source composition and geodynamic constraints on rough (visit [Link]/gems-gemology/spring-2023-
the Archean Fiskenæsset anorthosite complex, SW Green- gemnews-bright-orange-sapphire-greenland). This unusual
land,” Chemical Geology, Vol. 277, No. 1-2, 2010, pp. 1– stone was mined in late 2019 and heated in May 2022.
20). This deposit was initially known for producing Viala noted that it was a textbook example of a chromium
translucent to opaque ruby and pink sapphire, much of it trapped-hole (h•–Cr3+) chromophore (E.V. Dubinsky et al.,
Figure 28. A 1.28 ct heated pink round brilliant sap- Figure 29. A 0.89 ct heated orange oval brilliant sap-
phire. Photo by Robert Weldon; courtesy of Green- phire. Photo by Robert Weldon; courtesy of Green-
land Ruby. land Ruby.
Sweet Home mine rhodochrosite from 1888. At AGTA, New tourmaline pockets in San Diego County’s Pala Dis-
Ann Barker and Tori Lopez of Barker & Co. (Scottsdale, Ari- trict. At the AGTA show, Bill and Carl Larson (Pala Inter-
zona) exhibited a 7.94 ct rectangular step-cut rhodochrosite national, Fallbrook, California) shared details about new
(figure 30) with a provenance dating back more than a hun- pockets uncovered at the Tourmaline King mine. The first
dred years. The stone is from the Sweet Home mine in Col- was discovered in January 2022—the first major find at the
orado’s Alma Mining District, at an elevation of about 3,300 mine in more than a hundred years, and the first in South-
m in the Rocky Mountains. ern California since the “Big Kahuna” pocket at the Ocean-
Sweet Home was established as a silver mine in 1872. view mine in 2010. “We’ve hit off and on three or four
Miners initially discarded most of the rhodochrosite found pockets, some of which are very good,” Bill said.
in association with the silver ore because it interfered with The Larsons showed us several stones, including a
the amalgamation process used then in silver mining. But 16.96 ct emerald-cut green tourmaline (figure 31) from
the large, highly saturated, and nearly perfectly formed rough found near the first pocket in 2022. Bill said the
crystals later discovered there are some of the world’s finest green tourmaline is relatively uncommon for the Pala Dis-
rhodochrosite specimens. trict. “The green has actually been transparent enough to
Rhodochrosite was first described in the mineralogical
literature in 1813 based on specimens from what is now
Romania. In 1887, George F. Kunz wrote of gem-quality Figure 31. A 16.96 ct emerald-cut green tourmaline
rhodochrosite in Colorado, noting it was the first source from rough found near a new pocket at the Tourma-
with such large and transparent crystals. Most of the line King mine. Photo by Robert Weldon; courtesy of
rhodochrosite available worldwide was light pink, opaque, Pala International.
and often banded—typically used for beads, cabochons, and
carvings. This source introduced pink to red gem-quality
single-crystal rhodochrosite, which is rare. The gemstone
became more widely known in the late 1930s, after a Ger-
man gemologist found large volumes in Argentina’s Cata-
marca Province high in the Andes. (In Argentina, the use
of rhodochrosite dates back to the ancient Incas, who are
said to have believed it was the solidified blood of their
fallen rulers.)
The step-cut stone’s traceable history began in 1888,
when a shaft collapse resulted in a 32.61 ct cleavage frag-
ment. Miner Edward Abbott kept it and in 1925 gave it to
Denver businessman Edwin Spray, who later owned the
mine. The same year, Sweet Home miners found large spec-
Figure 38. “Rose Cut” 18K white gold and diamond Figure 39. “Event Horizon” earrings in 18K gold, dia-
earrings. The faceted diamonds are 1.5–2.0 mm in di- mond (0.07 carats total), and orange, mandarin, pink,
ameter. Photo by Robert Weldon; courtesy of Sean green, and blue sapphire (5.2 carats total). Photo by
Hill Designs. Robert Weldon; courtesy of Sean Hill Designs.
Zeki Karaca Jewelry: Luxury pens. Some of the most orig- designs and styles, he began making luxury pens and prod-
inal work we saw at the GJX show included bejeweled pens ucts three years ago. He first ventured into these new prod-
made by Turkish designer Zeki Karaca (figure 40). These ucts by crafting silver gemstone handles for Damascus
intricate pens feature exquisite details and fine craftsman- steel knives. After finding success there, he expanded to
ship in metalworking, enameling, engraving, inlay, and meet the demand for luxury pens, letter openers, and mag-
stone setting. In addition to pens, Karaca also creates other nifying glasses.
desk items such as letter openers and magnifying glasses Each pen takes about six months to design and craft.
(figure 41). All production steps are done by hand, making each item
Born in Istanbul, Karaca has 41 years of jewelry-making one of a kind. After designing an item, Karaca creates a sil-
experience, originally designing jewelry to sell in the Grand ver body using fold forming, with the folds created using
Bazaar. To apply his experience and creativity to different emery sheets. Engraving is executed by a master engraver
using different nibbed steel pens, and dimming is used to
emphasize the engraving. Karaka incorporates diamond,
Figure 41. Silver magnifying glass with 24K gold em- sapphire, emerald, and ruby into the designs and uses 24K
bellishments, inlay, carvings, and diamonds. Photo gold for design highlights. Miniature paintings, such as the
by Robert Weldon; courtesy of Zeki Karaca. peacock on the pen cap in figure 40 (left), are created by
hand with a small brush and then coated with a transpar-
ent enamel for protection. For micro-mosaics, gemstones
such as emerald are crushed and added to the pen body, as
seen in both pens in figure 40. The pen parts are welded to-
gether with a laser, and then the 24K gold nibs are added.
With high demand for his products from collectors,
Karaca continues to explore additional high-end objects as
well as custom designs for some clients.
Jennifer Stone-Sundberg and Mimi Travis
GIA, Carlsbad
Figure 42. A: This Lace Ring is crafted in 18K rose gold with blackened gold lace, featuring a cultured freshwater
pearl measuring 16.5 mm in diameter, enclosed by natural-color pink and lavender sapphire round brilliants weigh-
ing 2.86 carats total. The shank of the ring is embellished with 0.06 carats of diamonds. B: This Tahitian pearl Lace
Ring is created in 18K white gold with sandblasted and blackened gold lace. The cultured Tahitian pearl measures
16.0 mm and is surrounded by round brilliant diamonds, 1.35 carats total. The rubies in the shank weigh a total of
0.08 carats. C: A handmade doily crocheted by Smith’s grandmother. Photos courtesy of Brenda Smith.
blackened gold lace, rubies, and diamonds (figure 42B). In- Smith’s one-of-a-kind “Gibson Girl” earrings (figure 43)
spired by her grandmother’s handmade crocheted doily fea- are inspired by the Austrian symbolist painter Gustav
turing a pineapple motif (figure 42C), the rings were created Klimt. Klimt’s paintings combined realistic faces with geo-
as a tribute to her memory. In 2021, the white freshwater metric clothing, and Smith mirrored this style to create
pearl ring won Best Use of Pearls in the AGTA Spectrum this high-end piece of jewelry. The technique used to create
competition and the Tahitian pearl ring won the InDesign the girl faces is millefiori, which means “thousand flow-
Award in the category of Pearl Jewelry Over $5,000. ers” in Italian and produces slices from canes with concen-
tric and colorful patterns. Millefiori techniques can be used
to make jewelry, decorative objects, candy, and art pieces.
Figure 43. These “Gibson Girl” millefiori earrings in Creating these objects requires a skilled artisan who pos-
18K white gold contain Paraíba tourmalines (1.11 sesses a deep understanding of material properties, consid-
carats total), pink tourmalines (1.54 carats total), and erable experience, and patience. American artist Barbara
0.56 carats of aquamarine. Photo courtesy of Brenda McGuire handcrafted the complex face canes for the ear-
Smith. rings by arranging and embellishing polymer clays to create
a lifelike image. Though millefiori objects are commonly
used in decorative pieces, Smith’s design incorporates a
harmonious blend of colored gemstones expertly paired
and crafted to create a lively figure with a unique person-
ality and color scheme, making it an extravagant and ele-
gant piece of jewelry.
Si Athena Chen and Jennifer Stone-Sundberg
RESPONSIBLE PRACTICES
“There’s been a huge amount of progress over the past land at all, especially in Zambia, Kenya, and Malawi,”
two years,” Wheeler said. The funding helped Virtu Gem Maleta said. In Zambia, two of the mines—one emerald and
develop a strong foundation, she said, and grow enough one amethyst—were woman-owned, and in Kenya they
to be able to pass any chain of custody standard for large- worked with a young woman whose family owned a mine.
capacity buyers. One of Virtu Gem’s benefits is helping artisanal miners
While Virtu Gem has had success in all three countries, formalize their mining process. In Malawi, country coordi-
Wheeler said Kenya has seen the most because some in the nator Chiko Manda wanted to focus on rhodolite. Maleta
trade already had Ultra Tec cutting machines and were sell- said women account for roughly 80% of rhodolite produc-
ing to the international market. “After the first few pur- tion there (figure 51). Rhodolite is alluvial and best mined
chases we did, word spread,” she said. “People were
showing up with 50 gems at a time to process.” Miners can
also bring gems to the country coordinators for cutting. Figure 50. Rough tsavorite mined from a site in
Virtu Gem’s gemstones are cut in each country and Kenya. Photo courtesy of Virtu Gem.
tracked with Provenance Proof Blockchain. They include
amethyst, aquamarine, citrine, moonstone, rhodolite and
other garnets, in all three countries; emeralds in Zambia;
tsavorite in Kenya (figure 50); and color-change garnet in
Malawi. The three countries also produce tourmaline in
various colors, including pinkish orange (“sunset”) in
Malawi and Zambia and golden in Kenya and Malawi. Pro-
duction of morganite from newly discovered deposits in
northern Malawi recently began.
Virtu Gem has helped miners implement CRAFT Code
at four mines in Zambia, two in Malawi, and two in Kenya.
CRAFT Code is designed to improve safety, labor, and pay
conditions through education at the mines. Its components
include mine site certification, safety standards and equip-
ment, and environmental planning, including carbon data
tracking and reduction.
CRAFT Code has an emphasis on protecting women,
and Wheeler said they focused on women for the associated
training. Focusing on woman-owned mines was more diffi-
cult, however. “It’s a big challenge for women to own any
during the rainy season in Malawi, when the women are been easy,” he said. “But we have people who understand
busy tending their gardens. Virtu Gem worked with a the process, who know that the stone they are leaving with
young couple, Ben and Tamara, who did not have a mining Virtu will be sold, but also understand that if it’s not sold,
certificate. it will be returned. That is trust.”
“The chief of the Chewa people didn’t want the women “I was surprised by the lack of trust at the beginning,”
mining,” Wheeler recalled. “Ben had to go and prove him- Wheeler said. “We have to work hard to earn the trust from
self to the chief, that he wasn’t going to take advantage, everybody in the gemstone community. We couldn’t have
and that the women could still do their agriculture.” Ben done this without our partner, Monica Gichuhi, working
joined Virtu Gem’s calls with miners in Kenya and Zambia within the communities, and our country coordinators.”
who shared advice. “He ended up getting permission to She mentioned Caroline Muchira in Kenya, who is also a
mine on the land and the blessing of the chief,” she said. cutter and a GIA Graduate Gemologist; Manda in Malawi;
“He sent me on WhatsApp a picture that he had gotten his and Pauline Mundia in Zambia, a respected woman leader
certificate. He was so happy.” Maleta said that Ben recently whom everyone calls “Mama Pauline.”
received another land permit and is applying for a second “Living up to expectations is hard every single day,”
mining certificate. “That was a way we could still work Wheeler said. “Tucson is hard because we don’t own any-
with the women,” Wheeler said. thing on display. Those are people sending us their stones
Wheeler mentioned the danger of holding a large that they’ve invested in. Before, they would have just sold
amount of gemstones in an informal market, which Ben them and not invested in separating parcels and cutting.
and Tamara encountered with a quantity of rhodolite. “You That’s a lot of pressure. We’ve earned some of that trust,
have the paradox of the women’s safety,” she said. “Every- and we really have worked hard to earn that.”
body hears about it, and you get all these other dealers and “It’s a dream come true for many to have their stones
traders coming in. How are they going to get a fair price? sold at this level,” Maleta said. “For us, for the country, for
Yet they can’t hold on to it.” She said Ben called his friends the people who are trading, the future is bright.”
and pleaded with them to purchase some of the rhodolite. Erin Hogarth
She would like to see a formal system to address this type
of scenario.
Maleta said the past four or five years have seen an in- SYNTHETICS AND SIMULANTS
flux of Kenyans and Zambians to Malawi to buy gems,
some of whom export them back home and misrepresent Luminescent synthetic garnet-like crystals. At the 22nd
the source country. By exporting directly from Malawi, Street show, the author spoke with Tim Challener of Tur-
Virtu Gem has improved supply chain transparency. tle’s Hoard (Raleigh, North Carolina), who was selling some
Maleta said Virtu Gem pays more than the informal unique rough and faceted luminescent synthetic garnet-like
market, but convincing people to participate can be a chal- crystals, which he referred to as “lumogarnets.” After 12
lenge. “To have someone leave a stone with you and years in the gem business, Turtle’s Hoard began selling only
wait—for maybe two months, three months—it hasn’t laboratory-made materials in March 2022. Challener noted
importance of responsible mining and sustainability in the during the AGTA GemFair in Tucson. Guergova, the first
industry. student from the London campus to win the award, designed
In 2021, GIA provided a grant to Mercury Free Mining a stunning bracelet featuring swans to represent together-
(MFM) and the Alliance for Responsible Mining (ARM). ness and loyalty (figure 57).
New methods for concentrating gold continue to be ex- Created in partnership with the Gianmaria Buccellati
plored and tested with the goal of significantly reducing, Foundation in 2018, the award recognizes outstanding talent
or even eliminating, the use of mercury in gold mining. in design among GIA students worldwide. Larry French,
Erica Zaidman chief officer for North America strategies at the foundation,
GIA, Carlsbad said, “On behalf of the Gianmaria Buccellati Foundation,
we want to congratulate Ms. Sara Guergova, this year’s win-
ner, plus all the other finalists whose work so enriched this
ANNOUNCEMENTS year’s competition. We also want to recognize the talented
GIA design instructors who helped guide the students on
Sixth annual Gianmaria Buccellati Foundation Award win- their way to the final judging in Tucson.”
ner. Sara Guergova, a graduate of GIA’s Jewelry Design pro- The 2023 Gianmaria Buccellati Foundation Award for
gram in London, received the sixth annual Gianmaria Excellence in Jewelry Design competition is underway and
Buccellati Foundation Award for Excellence in Jewelry De- open to students in GIA’s Jewelry Design courses who meet
sign. The 12 finalists and winner were announced at the GIA the eligibility requirements. Visit [Link]/buccellati-
Alumni Collective’s “Night at the Museum” event held foundation-award-jewelry-design for more information.
The pendant on the right is a miniature recreation of the “Bahia,” a massive rutilated
quartz fashioned by Glenn Lehrer and Lawrence Stoller. Each pendant in the collection
is carved from leftover raw material. The photo on the left is by Harold and Erica Van
Pelt; courtesy of Glenn Lehrer. The photo on the right and the rest of the photos in this
gallery are by Robert Weldon.
This suite of cat’s-eye topaz cabochons of unknown origin features a 135.80 ct center stone. Courtesy of Mayer
& Watt.
This brooch features a 13.27 ct Imperial topaz sur- In this beautifully matched pair of natural pearl ear-
rounded by 8.50 carats of diamonds, mounted in 18K rings, each 10 ct round pearl sits atop an astonish-
yellow gold. Courtesy of Jewelerette & Co. ingly large 32 ct pearl drop. Courtesy of Sima G. Ltd.
A spray of “mango” quartz measuring 92 × 103 mm from the Boyacá Province in Colombia. The yellow coloration
is believed to be due to the mineral halloysite. Courtesy of Cornerstone Minerals.
This naturally formed azurite disc on kaolinite ma- A stunning pair of Alexandre Reza 18K gold earrings.
trix, accompanied by a cluster of malachite, hails In this design, 112 diamonds (totaling 7.86 carats)
from the Malbunka copper mine in Northern Terri- dangle from two emeralds (totaling 2.12 carats).
tory, Australia. It measures 123 × 140 mm. Courtesy Courtesy of Jardin Jewels.
of Fine Art Minerals and Ghulam Mustafa.
Rough and carved hemimorphite, weighing 173.35 ct A vintage Fred of Paris demi-parure of earrings and a
and 112.26 ct, respectively. Courtesy of Evan Caplan. bangle, set with diamonds, rubies, emeralds, and sap-
phires. Courtesy of Jardin Jewels.
This aquamarine spray cluster from Skardu, Pakistan, measures 160 × 102 mm. Courtesy of Fine Art Minerals and
Ghulam Mustafa.
Indicolite from Afghanistan. The 116.7 ct crystal is Earrings and necklace in a jellyfish motif, set in 14K
from Nuristan Province, and the 9.39 ct cut gem is yellow gold. The mabe pearls are from the Sea of
from Kunav Province. Courtesy of Dudley Bauwet Cortez. Courtesy of Columbia Gem House.
Gems and Mountain Minerals International.
Master cutter Mark Gronlund combines natural Oregon A Cartier Les Oiseaux Libérés diamond, emerald, and
sunstone with unheated Nigerian pink tourmaline in this sapphire ring crafted in 18K white gold. Courtesy of
7.35 ct doublet, shown in table and profile views. Cour- Jardin Jewels.
tesy of Desert Sun Mining and Gems.
Aptly named the “Ring of Fire,” this Ethiopian opal in matrix displays a square of dark opal surrounded by a ring
of white opal. Courtesy of Ellie Gem Arts.
This bicolor spodumene is from Nuristan Province, Afghanistan. Terminations of the crystal appear to mimic the
mountain range from which it was mined. Courtesy of Dudley Blauwet Gems and Mountain Minerals International.
Vintage diamond and carved emerald bracelet designed An art nouveau enameled necklace in a floral motif in-
by Alexandre Reza. Courtesy of Jardin Jewels. corporating 20 seed pearls, four natural freshwater
pearls, and a freshwater Mississippi dogtooth pearl.
Courtesy of Bernard Nacht & Co./Under the Crown.
This horn-shaped boulder opal measures 75.5 × 15.9 × 4 mm and weighs 74.20 ct. Courtesy of Dufty Weis Opals Inc.
Additional RTX and X-ray computed microtomogra-
REGULAR FEATURES phy (μ-CT) analyses were conducted to further study the
internal structures. RTX imaging of pearl A revealed a
non-bead cultured pearl used as a “bead” nucleus (figure
COLORED STONES AND ORGANIC MATERIALS 59). A light gray core surrounded by organic-rich concen-
tric growth structures followed by finer growth arcs was
Pinctada radiata atypical bead cultured pearls from the visible. An obvious demarcation with a small organic tail-
UAE. Pearling is embedded in the culture and traditions of like feature just below the surface overgrown with cul-
everyday life in the United Arab Emirates (UAE), especially tured nacre was also apparent. The lack of growth arcs in
in the trading center of Julfar. Abdulla Al Suwaidi, grand- the nacreous layers was due to rapid growth during the
son of one of the last traditional pearl divers in the UAE, culturing process (“Atypical ‘beading’ in the production
took on the challenge of reviving the country’s pearling in- of cultured pearls from Australian Pinctada maxima,”
dustry. He succeeded in establishing the Suwaidi Pearl GIA Research News, February 13, 2017). Similarly, pearl
Farm in Al Rams, Ras Al Khaimah (RAK), in 2005. B revealed a natural pearl used as a “bead” nucleus (figure
Suwaidi’s cultured pearl farm is recognized as the first of 60), with a very small but clearly visible dark gray core
its kind in the Arabian (Persian) Gulf region. surrounded by faint growth arcs. As with pearl A, a dis-
GIA’s Mumbai laboratory recently examined a quantity tinct demarcation with organic-rich areas and a small or-
of cultured pearls obtained from the farm. The parcel con- ganic tail-like feature were evident just below the surface
tained variously shaped white to cream-colored pearls. Ex- overgrown with cultured nacre. X-ray computed micro-
amination by real-time microradiography (RTX) showed a tomography analysis of both samples revealed clearer im-
variety of different internal structures including bead and ages of the demarcation between the “bead” pearls used
non-bead cultured pearls, but two pearls in particular (fig- as nuclei and the cultured nacre overgrowths.
ure 58) revealed very interesting structures and were con- Optical X-ray fluorescence examination did not show
firmed to be samples from atypical “bead” culturing any fluorescence in either sample. Energy-dispersive X-ray
experiments conducted by the farm. Pearl A was light fluorescence spectrometry revealed manganese levels
cream and near-round, weighing 0.87 ct and measuring below detection limits and strontium levels of 1130 ppm
5.13 × 4.93 mm, while pearl B was cream and button for pearl A and 1446 ppm for pearl B. The results from both
shaped, weighing 0.94 ct and measuring 5.42 × 5.12 × 4.93 testing methods were consistent with a saltwater growth
mm. When viewed under 40× magnification, both pearls environment. The ultraviolet/visible reflectance spectra
exhibited a smooth surface and possessed typical nacreous collected for both pearls showed features around 435 and
overlapping aragonite platelets. 460 nm and an additional weak band at 495 nm. These fea-
tures are similar to spectral observations previously separate from some natural pearls. This would be espe-
recorded for natural Pinctada radiata pearls (A. Al-Alawi cially true of the two samples featured in this report: If ei-
et al., “Saltwater cultured pearls from Pinctada radiata in ther of them were drilled and mixed in strands with
Abu Dhabi (United Arab Emirates),” Journal of Gemmol- natural Gulf pearls, an experienced gemologist would find
ogy, Vol. 37, No. 2, 2020, pp. 164–179). Raman analysis it difficult to separate them from the other pearls. The au-
using 514 nm laser excitation was carried out on the sur- thors have encountered natural pearls with similar dis-
faces of both pearls, and a doublet at 704/705 cm–1 as well tinct boundaries. It should also be noted that the aBCPs
as a peak at 1085 cm–1, indicative of aragonite, were ob- produced at the Suwaidi farm are the result of successful
served. Weak polyenic pigment-related peaks at 1130 and experiments, and they are not commercially available at
1540 cm–1 were only observed for pearl B and were associ- the time of this writing. The farm continues to conduct
ated with its cream coloration. The photoluminescence various experiments and aims to restore the UAE’s place
spectra were also consistent with the Raman results and in the global market by producing the finest Pinctada ra-
displayed high fluorescence together with the aragonite diata cultured pearls available.
peaks, typical of most nacreous pearls.
Abeer Al-Alawi
Using lower-quality pearls (both nacreous and non-
GIA, Global
nacreous), gemstones, and other materials as “bead” nuclei
has been a known practice for the last decade (“Chasing cul- Lubna Sahani
tured pearls at SSEF: Cultured pearls using a natural pearl GIA, Mumbai
as a bead,” 2020, [Link]
Nicholas Sturman
pearls-at-ssef-cultured-pearls-using-a-natural-pearl-as-a-
Bangkok
bead/). Although not seen on a regular basis, atypical
“bead” cultured pearls (aBCPs) are encountered in labora- Chunhui Zhou
tories from time to time and can be very challenging to GIA, New York
Bead cultured abalone pearls from Chile. Abalone is the and various methods have been attempted over the years
common name of the marine mollusk species that belongs (C.Y. Wentzell, “Cultured abalone blister pearls from New
to the Haliotis genus. Various abalone species are distrib- Zealand,” Fall 1998 G&G, pp. 184–200; M. Monteforte and
uted worldwide along cold coastal waters. They live in H. Bervera, “Abalone pearl culture on the west coast of the
rocky habitats, attaching firmly with their muscular foot. Baja California peninsula, Mexico,” World Aquaculture,
Abalone is highly prized for its meat, shell, and pearls. Due 2010, pp. 12–17). However, due to abalone’s hemophilia
to a marked decrease of abalone populations, harvesting and poor tolerance for chemicals and handling, any signif-
wild-caught abalone is heavily regulated. Thus, approxi- icant cut could cause major bleeding, and the nucleation
mately 95% of the global abalone supply comes from farms and implantation procedures could induce infection that
around the world, in countries such as China, South Korea, prohibits the mollusk from producing nacre. Therefore, the
South Africa, Chile, Australia, Taiwan, Japan, the United success rate of bead cultured (BC) abalone pearls was al-
States, and New Zealand (P.A. Cook, “Worldwide abalone ways low and the pearls were of unmarketable quality.
production statistics,” Journal of Shellfish Research, Vol. After 10 years of experimenting, scientists from the Uni-
38, No. 2, 2019, pp. 401–404). versity of Antofagasta, Chile, have successfully created
Abalone’s ear-shaped shells and pearls are known for abalone BC pearls using a patented method for producing
their unique, vibrant iridescent nacre, which is sought after free pearls in abalone. Twelve of their cultured pearls and
in jewelry and decorative items. The iridescence phenome- two abalone shells with a cultured shell blister attached (fig-
non is also known as “orient,” and it is attributed to inter- ure 61) were submitted to GIA for study in May 2022. They
ference and diffraction of light in the multilayered aragonite were the pilot crop of a new pearl culturing technique using
platelet microstructure and organic components. Due to the traditional freshwater shell bead nuclei (5 to 8 mm) inserted
rarity of natural abalone pearls, most abalone products used into grafting channels in the visceral mass of Haliotis
in jewelry today are either abalone shells or assembled cul- rufescens (red abalone) imported into Chile from Mexico in
tured shell blisters (also known as “mabe pearls”). the 1990s (figure 62, left) for abalone farming. The BC pearl
The culturing of whole pearls in abalone mollusks cultivation takes place during the last 24–28 months of the
started around the same time as shell blister culturing for abalone culture process that usually takes 48–52 months,
producing mabe pearl (assembled cultured shell blister), allowing the abalone meat and the pearl to be harvested at
the same time. The facilities include an aquaculture recir- strong iridescence, along with patches and stripes of dark
culation system in eight raceways of 5000 liters, with con- brown organic materials. They exhibited a variety of
tinuous aeration by blowers and a culture water flow of 5000 baroque forms, and four samples possessed horn or tooth
liters per hour (figure 62, right). The local kelp species Lesso- shapes often found in natural abalone pearls. A character-
nia trabeculata obtained from natural, sustainably managed istic underlying botryoidal-like surface structure, usually
sources is used to feed the mollusks twice a week. Despite observed on natural abalone pearls and shells, was also
a high rate of bead nucleus rejection, the survival rate of the present (Fall 2015 Lab Notes, pp. 319–320). Real-time mi-
mollusks after grafting has been 99% and is currently at croradiography (RTX) revealed a round bead nucleus in the
15,000 grafted mollusks per trial, according to the farm. majority of samples, and the nacre layer thickness sur-
The cultured abalone pearls produced using this rounding the bead nuclei ranged from 0.10 to 1.20 mm (fig-
method displayed multicolored nacreous surfaces due to ure 63). One sample lacked a bead nucleus and was
0
100 300 500 700 900 1100 1300 1500
RAMAN SHIFT (cm –1)
identified as a non-bead cultured (NBC) pearl. Its layered reflectance and photoluminescence spectra, and Raman
growth with void-related features resembled the internal spectra showed high fluorescence background and weak
structure commonly found in natural abalone baroque peaks of aragonite at 704 and 1085 cm–1 (figure 64). Energy-
pearls. dispersive X-ray fluorescence analysis revealed all the sam-
Ten natural abalone pearls were selected for spectro- ples had very low or below detection limit manganese
scopic and chemical comparison with the cultured pearl content and high levels of strontium ranging from 1100 to
samples, and both types of samples showed similar results. 5000 ppm. High iodine levels were also detected in most
No specific patterns were observed in ultraviolet/visible samples, which is common in abalone. Trace element con-
centrations determined by laser ablation–inductively cou-
pled plasma–mass spectrometry (LA-ICP-MS) were
compositionally similar in both sample types. However,
Figure 65. The cultured and natural abalone pearl
the cultured samples contained lower boron and higher
samples were compositionally similar in trace ele-
potassium contents. All four tested spots of the NBC sam-
ment concentrations determined by LA-ICP-MS.
ples could be clearly separated from natural samples in the
However, the cultured samples contained lower
plot of boron vs. potassium contents (figure 65). Since the
boron and higher potassium than the natural pearls.
one NBC pearl showed an internal structure similar to that
All four tested spots of the NBC samples are clearly
of natural abalone pearls, the plot can potentially be used
separated from natural samples in this plot.
to differentiate NBC pearls from natural samples. How-
ever, further study on both sample types is required. Addi-
B VS. K tionally, all abalone samples showed higher strontium
concentrations than Pinctada species previously studied.
300 The success of abalone BC pearl production could be a
promising addition to the gem and jewelry industry, and
Spot 3
this study provided useful information for future reference.
K (ppm)
The gemological examination of these Pinctada radi- toq ruby and pink sapphire deposit, located 160 km south
ata pearls proved very rewarding, especially with regard to of Nuuk.
their internal structures. Research into what causes the The corundum extracted at Aappaluttoq is heated in
formation of a pearl in the wild is ongoing. Hence, finding air at temperatures over 1500°C for several hours, with
these minute shells that may be the initiation of growth some flux added. In rare cases, the heating significantly al-
in these two natural pearls is a truly rare circumstance. ters the color of light pink and near-colorless sapphire, re-
Nishka Vaz sulting in fancy-color sapphire. GIA recently studied a
GIA, Mumbai parcel of 22 of these fancy-color sapphires mined and
treated by Greenland Ruby (figure 70).
Nicholas Sturman
A combination of ultraviolet/visible/near-infrared (UV-
Bangkok
Vis-NIR) spectra and trace element chemistry using laser
Abeer Al-Alawi ablation–inductively coupled plasma–mass spectrometry
GIA, Global (LA-ICP-MS) were collected at GIA in Bangkok to identify
the causes of color. For full quantification of the chro-
Color study of fancy sapphire from Greenland. Over the mophores, it is necessary to do this analysis in oriented,
past 70 years, several ruby and pink sapphire localities have clean samples with a known path length. Since most of the
been documented in the region of Greenland’s capital city, Greenland material is polished as cabochons and contains
Nuuk (P.W.U. Appel and M. Ghisler, “Ruby- and sap- some inclusions, it is very challenging to calculate or even
phirine-bearing mineral occurrences in the Fiskenaesset, estimate the absorption coefficients. We limited ourselves
Nuuk and Maniitsoq regions, West Greenland,” GEUS, to a rough interpretation of the chromophores based on the
Geological Survey of Denmark and Greenland, 2014). Sev- shape of the spectra. Orientation of the samples was esti-
eral of these localities are currently exploited on a small mated based on the pleochroism.
scale by the local communities. In 2017, Greenland Ruby Additionally, we could not precisely identify which
A/S started a large-scale mining operation at the Aappalut- area of the stone was analyzed during the spectroscopy, and
thus all UV-Vis spectra were bulk measurements and com- Greenland ruby, this comes down to the balance between
bined the color of different zones. In contrast, the LA-ICP- Mg2+ vs. Ti4+, Si4+, and H+. Since the stones have all been
MS analysis was performed at very specific spots, allowing treated in air (oxidizing atmosphere), we can assume that
the analysis of specific zones. H+ has diffused out of them. With the method used to meas-
The literature describes six chromophores responsible ure trace elements (LA-ICP-MS with a quadrupole MS), we
for color in natural corundum (E.V. Dubinsky et al., “A cannot correctly quantify the Si4+ content in these stones.
quantitative description of the causes of color in corun- The possibility that Si4+ plays a role in the color cannot be
dum,” Spring 2020 G&G, pp. 2–28). Four of the chro- excluded. Regardless, there is no indication here that Si4+ is
mophores from that study are responsible for the colors in required to tilt the balance of chromophores when compar-
this suite. ing trace elements vs. observed color. Since we do not aim
Most stones from the Aappaluttoq deposit are colored to quantitatively analyze the color, we ignore any potential
by the Cr3+ chromophore, giving them their typical pink to presence of Si4+. This means that the concentrations of Mg2+
red color (figure 71). The intensity of the color is directly and Ti4+ are the determining factors: Only if the amount of
linked to the concentration of Cr3+, which can go up to sev- Mg2+ is larger than the Ti4+ concentration can trapped holes
eral 1000 ppma, and in exceptional cases even to 15,000 develop in sapphire from Greenland.
ppma. Most of the lighter-colored material has a concen- Two ions in sapphire can pair with trapped holes: Fe3+
tration of a few 100 ppma, resulting in a pink color. and Cr3+. Since the trapped hole preferentially pairs with
Depending on the orientation, it can appear more pur- Cr3+, this is the chromophore observed in these stones. The
ple (when viewed through the c-axis). In some cases, this quantity of trapped holes that can form in corundum is
is so strong that the face-up color of the stone is modified very low, and as such, not all the Cr3+ couples with a
to an extent that it cannot be defined as ruby or pink sap- trapped hole. The final color will be a combination of the
phire and falls into the fancy reddish purple range. Some trapped hole color and the pure Cr3+ chromophore, result-
of the stones develop a more orangy tone after treatment. ing in a combination of pink to red and orange colors.
(A bright orange oval brilliant seen at the 2023 Tucson Trapped holes are very strong coloring agents that can have
shows is highlighted on pp. 115–116 of this issue.) This a major impact even when their concentration is very low.
color can be attributed to the creation of trapped holes in The Fe3+ chromophore is the weakest one encountered
combination with Cr3+ (figure 72). in natural corundum. Very high concentrations of Fe3+ are
To create trapped holes, the chemical balance in the required to create a yellow color, often exceeding several
stone needs to be correct. Only when a stone is acceptor thousand ppma. Since the Greenland rubies have a maxi-
dominated will trapped holes be present. In the case of mum iron concentration under 1500 ppma, this chro-
mophore creates only a very weak yellow color (figure 73). common, which makes it very difficult to notice any color
Other common chromophores are much stronger and more contribution by Fe3+. Only when the Cr3+ concentration is
UV-VIS-NIR SPECTRA
Figure 73. This plot
shows the o-ray spec-
trum of a pale yellow
sample (black) and a
modified o-ray spec-
ABSORBANCE
O-ray
trum where some con-
Cr 3+ removed tribution by Cr3+ is
subtracted (blue). When
the Cr3+ spectrum is re-
moved, a pure Fe3+ spec-
trum remains. This
300 350 400 450 500 550 600 650 700 750 800
spectrum is character-
WAVELENGTH (nm) ized by the double peak
at 377–388 nm and one
Mg Ti V Cr Fe Ga [Ti]-[Mg] at 450 nm. The ratio of
the 388 to 377 nm band
S269612 Spot 1 16 14 10 96 1150 12 –2
suggests a relatively
S269612 Spot 2 13 12 9 81 1136 13 –1 low Fe3+ chromophore
concentration, which
S269612 Spot 3 14 12 9 76 1143 14 –2 matches the observed
Detection limits 0.011 0.033 0.004 0.068 0.824 0.002 color and analyzed
(ppma) chemistry (in ppma).
UV-VIS-NIR SPECTRA
E-ray
O-ray
Figure 74. The ex-
tremely low Cr3+ con-
ABSORBANCE
Liberian ruby. A gemological education can often prove quartz, and possible spinel. Samples were purchased from
useful in the most unusual of circumstances. On a recent the miners for analysis, which came as a welcome surprise
trip to rural Liberia with the Japan-based NGO Diamonds since they were unaware that these colored stones could
for Peace (DfP), the author discovered a previously unac- carry any value (figure 76, left).
knowledged source of ruby. The original purpose of the The author subsequently analyzed all the samples at
visit was to deliver a rough diamond grading and valuation the Gemmological Certification Services (GCS) laboratory
workshop to the miners working and living in 17 commu- in London. Using advanced and standard gemological test-
nities across Liberia. During the trip, the author stayed in ing, the identity of all the presumed gem-quality minerals
the town of Weasua, one of the larger mining communi- of the collected specimens was confirmed. Particular focus
ties, to experience the standard of living and the general was placed on the rubies due to their apparent abundance
working conditions of the miners. The poverty is extreme. at the mine site, with the hope of providing another means
Most homes are without electricity, facilities, or running of income for this community.
water, and only three functional water pumps exist for a All ten samples tested were identified as corundum.
population of 5,000, all of which place the health and the Due to the nature of the rough material, standard testing
well-being of this community at risk. DfP has been work- was limited, beyond measuring specific gravity—which,
ing with this community since 2018 and has made signif- averaging 4.0 across all samples, supported corundum. The
icant inroads in supporting and improving the lives of these ultraviolet/visible/infrared absorption spectrum, with its
miners, but there is a long way to go, and strategies to aid chromium-associated features, was also consistent with
their mission are continually being developed. ruby. X-ray fluorescence analysis of the trace element
It was therefore fortuitous that during the visit, the au- chemistry revealed 1029–2377 ppm iron and 721–2915
thor learned that there were other promising gem-quality ppm chromium, with low levels of gallium (54 ppm) and
minerals in the alluvial gravels the miners were collecting vanadium (53 ppm).
in their pursuit of diamond (figure 75). Upon initial inspec- Generally, the color of the alluvial material collected
tion while on-site, the author noted material resembling ranged from pinkish gray to a deep purplish red, with sizes
corundum (primarily ruby), garnet, topaz, rock crystal varying from 6 to 14 mm (1.45–15.90 ct), although the au-
thor was shown larger pieces on-site. All of the material gemstone reportedly from Tanzania (figure 77). Its refrac-
showed a moderate to weak red fluorescence response in tive index of 1.714 and hydrostatic specific gravity of 3.59
long-wave UV and inert to weak red in short-wave UV,
consistent with high-iron ruby due to the quenching of
Cr3+-associated fluorescence by iron. The majority of the Figure 77. This faceted purple spinel, weighing 0.51 ct
samples showed lamellar twinning, surface-reaching frac- and measuring 5.20 × 4.17 × 3.10 mm, was reportedly
tures, and iron staining. The material was translucent to from Tanzania. Photo by Jinlin Wu.
opaque, meaning that clear observation of any other inclu-
sions was limited.
Although the material is not considered high-quality
ruby, some of the better pieces have been polished to create
attractive cabochons (figure 76, right). Diamonds for Peace
is currently developing a business plan to monetize this
material for the benefit of the community. The GCS labo-
ratory will continue to support Diamonds for Peace as that
organization explores this new potential avenue of income
for the miners of Weasua.
Beth West
Gemmological Certification Services, London
0.7
Figure 78. The UV-Vis-
ABSORBANCE
0.4
0.3
0.2
350 400 450 500 550 600 650 700 750 800
WAVELENGTH (nm)
indicated spinel. Its ultraviolet/visible/near-infrared (UV- As a rock-forming mineral, forsterite (Mg2SiO4) itself
Vis-NIR) absorption spectrum was characterized by a se- is common, especially in marble-hosted spinel. However,
ries of absorption bands centered at 555 nm and several it is rarely observed in Tanzanian spinel and has been re-
iron-related small bands centered at around 371, 385, 461, ported only once to our knowledge (E. Gübelin and J.I.
and 478 nm, as well as an extremely weak band at ~625 Koivula, Photoatlas of Inclusions in Gemstones, Vol. 2,
nm for Co2+ (figure 78). This absorption profile revealed Opinio Publishers, Basel, Switzerland, 2005, 829 pp.).
that iron (Fe2+ and Fe3+) was the main coloring element
(P.M. Belley and A.C. Palke, “Purple gem spinel from Viet-
nam and Afghanistan: Comparison of trace element chem- Figure 79. A colorless subhedral forsterite (Fo) inclu-
istry, cause of color, and inclusions,” Fall 2021 G&G, pp. sion and a dolomite (Dol) inclusion with an unknown
228–238). dark material attached. Photomicrograph by Jinlin
Energy-dispersive X-ray fluorescence analysis was per- Wu; field of view 0.66 mm.
formed to determine the sample’s trace element concentra-
tion, which showed 10950 ppmw iron, 963 ppmw zinc, 52
ppmw chromium, 94 ppmw vanadium, and 9 ppmw cobalt.
These results were similar to the chemical features of rep-
resentative purple Tanzanian spinel: extremely high iron
content, medium zinc content, and low chromium and
vanadium contents (G. Giuliani et al., “Pink and red spinels Fo
in marble: Trace elements, oxygen isotopes, and sources,”
Canadian Mineralogist, Vol. 55, No. 4, 2017, pp. 743–761).
Microscopic observation revealed a colorless subhedral
mineral, a dolomite with an unknown dark material at-
tached (figure 79), and oriented short needles (figure 80).
Raman spectroscopy identified the colorless mineral as
forsterite. According to the RRUFF database (B. Lafuente Dol
et al., [Link]
peaks at 822, 855, 918, and 963 cm−1 were consistent with
the main peaks of forsterite (figure 81).
RAMAN SPECTRA
855
918 963
225 373 432 543 592
and is active in absorption and luminescence, is widely National Gemstone Testing Center’s (NGTC) Beijing
considered an identifying feature of CVD diamond. Gen- laboratory recently received a 1.63 ct grayish blue princess
erally, the SiV– center is detected by photoluminescence cut (figure 82, left) for identification. Standard testing iden-
spectroscopy and is not observed using absorption spec- tified it as a CVD synthetic diamond. The sample showed
troscopy for most CVD synthetics due to the low silicon an even color distribution. Microscopic investigation re-
content. The absorption spectra may reveal the presence vealed abundant non-diamond carbon inclusions in the
of the SiV– center in the case of a relatively high silicon form of both crystals and clouds, with the clouds distrib-
content, but rarely in amounts significant enough to affect uted along the growth layer (figure 82, right). The
the color. When the silicon content becomes particularly visible/near-infrared (Vis-NIR) spectrum (figure 83),
high, the absorption of SiV– is in sufficient concentration recorded at liquid nitrogen temperature, included a strong
to influence the bodycolor of a diamond. It has been re- broad SiV– center defect at 737 nm next to an equally
ported that the color of silicon-doped blue CVD diamonds strong GR1 center. The diamond’s grayish blue bodycolor
produced by the PDC Company is attributed to strong ab- was attributed to both the strong GR1 center and the high
sorption of the rather intense SiV– center (A. Peretti et al., intensity of the SiV– center, which produced preferential
“New generation of synthetic diamonds reaches the mar- absorption in the red part of the spectrum. In addition,
ket (Part A): Identification of CVD-grown blue diamonds,” weak absorptions at 830, 856, and 946 nm (the SiV0 center)
Contributions to Gemology, No. 14, 2013, pp. 3–20). were observed, which were also reported in CVD synthetic
VIS-NIR SPECTRUM
737
0.55 741
PL SPECTRA
503.5
Figure 84. DiamondView imaging showed green fluo- 50000
A 486.3
rescence with blue dislocations. The diamond also
INTENSITY (counts)
revealed a layered growth structure, indicating a 40000
start-stop cycling growth process typical of CVD dia-
mond, as CVD diamond growth takes place layer by 30000 488 490 494
layer on the top surface of the growing crystal. Image
by Xiaoyu Zhang. 20000 486 490 494
Diamond
Raman
10000 503.2 505 530.7 540.7 552.4
986
400
silicon content of this diamond was so high that it produced Under short-wave ultraviolet (SWUV, 254 nm) radia-
strong absorption in the red range of visible light and affected tion using a standard viewing UV cabinet and a De Beers
the color of the diamond together with the GR1 center. PhosView instrument, the stone displayed a mix of
Wang Yang (wangyang@[Link]), Xiaoyu Zhang, strong greenish blue and medium orange zoned fluores-
and Zhonghua Song cence and phosphorescence (figure 86, bottom). The col-
NGTC, Guangzhou and Beijing ored phosphorescing areas decayed at different rates, with
the greenish blue fading faster than the orange (~90 sec-
onds vs. ~240 seconds, with a half-life of about 25 and 35
HPHT-grown colorless diamond displaying unusual phos-
seconds, respectively).
phorescence effects. Phosphorescence longer than 10 sec-
Deep-UV (<225 nm) imaging demonstrated a strong
onds in reaction to ultraviolet radiation is regularly
greenish blue fluorescence with a clear cuboctahedral struc-
observed in colorless to near-colorless and blue-colored dia-
ture associated with HPHT growth (figure 87). After removal
monds grown by a high-pressure, high-temperature (HPHT)
technique. The gemological laboratory of Stuller Inc. re-
cently tested an HPHT-grown colorless (approximately E
color grade with a blue-gray overtone) oval brilliant dia- Figure 87. Deep-UV imaging of the 0.71 ct colorless
mond weighing 0.71 ct that showed unusual fluorescence diamond showing a cuboctahedral-structured lumi-
and phosphorescence reactions. nescence associated with HPHT growth. Image by
When exposed to a long-wave ultraviolet (LWUV, 365 Guy Borenstein.
nm) source for 60 seconds using a standard UV viewing
cabinet, the stone emitted a gradually increasing strong or-
ange fluorescence, followed by a long-lasting noticeable
phosphorescence (~150 seconds, figure 86, top). The fluo-
rescence and phosphorescence reactions demonstrated a
nonuniform color distribution. Similar results were ob-
served using other light sources, including 395 nm UV
LED, 405 nm blue laser, a tungsten incandescent flashlight,
and a fiber-optic halogen unit.
Given that orange phosphorescence can also be gener-
ated by low- and non-UV light sources, further analysis
was performed using a series of spectral bandpass filters
to identify other wavelengths that stimulate the orange
phosphorescence. Testing demonstrated that medium- to
strong-intensity light centered at around 430 nm produces
the excitation.
HPHT-grown diamond
1.5
revealed it was type IIb
with relatively high lev-
1.0 els of uncompensated
boron (for a colorless
diamond) at 4089, 2929,
0.5
2800, and 2455 cm–1.
0
6000 5000 4000 3000 2000 1000 0
WAVENUMBER (cm–1)
from the excitation source, the stone displayed a phospho- length reinforces the theory that the recorded orange phos-
rescence reaction similar to the reaction under SWUV. phorescence is of a different donor-acceptor pairing.
Infrared spectroscopy revealed a type IIb diamond with Light of 430 nm wavelength can be found in most fluo-
relatively high levels of electrically uncompensated boron rescent and all incandescent indoor light sources, as well as
at 4089, 2929, 2800, and 2455 cm–1 (figure 88). Photolumi- the desk lamps and color grading cabinets found in gemo-
nescence spectroscopy with 532 nm laser excitation at liq- logical laboratories. Therefore, considering the possibility of
uid nitrogen temperature (77K) showed no results, except more diamonds with this property in the market, their phos-
for the diamond’s first- and second-order Raman spectrum phorescence produced from visible light makes it challeng-
peaks, a common tendency in HPHT-grown colorless dia- ing to assign a color in the colorless to near-colorless range
monds (S. Eaton-Magaña et al., “Observations on HPHT- for these diamonds during grading. Even under standard non-
grown synthetic diamonds: A review,” Fall 2017 G&G, pp. or low-UV output 6500K fluorescent bulbs, the orange lu-
262–284). minescence generated by the source becomes noticeable,
The two phosphorescence colors emitted and their rel- adding a yellowish overtone to the blue-gray bodycolor and
atively long duration are well-known properties of HPHT- changing its apparent color grade to approximately F to G.
grown diamonds (S. Eaton-Magaña and R. Lu, Such a change may impair the diamond grader’s ability to
“Phosphorescence in type IIb diamonds,” Diamond and accurately assess the stone’s bodycolor.
Related Materials, Vol. 20, No. 7, 2011, pp. 983–989; Eaton- Guy Borenstein and Sean O’Neal
Magaña et al., 2017), and a blue-orange luminescence com- Stuller Inc.
bination in one gem was also previously reported Lafayette, Louisiana
(Eaton-Magaña and Lu., 2011; B. Deljanin et al., “NDT
breaking the 10 carat barrier: World record faceted and gem-
quality synthetic diamonds investigated,” Contributions to SYNTHETICS AND SIMULANTS
Gemology, Vol. 15, No. 1, 2015) but of weaker intensity.
The laboratory-grown diamond’s property of bicolor, decay- Synthetic color-change wakefieldite. Author AA, a gem-
varying phosphorescence has been previously reported as stone cutter and collector of rare synthetic gems, recently
well (K. Watanabe et al., “Phosphorescence in high-pres- submitted one rough and one faceted stone to GIA for sci-
sure synthetic diamond,” Diamond and Related Materi- entific examination. The material, sourced from RG Crys-
als, Vol. 6, No. 1, 1997, pp. 99–106; Eaton-Magaña and Lu, tals in Bangkok, was stated to be Czochralski-pulled,
2011; Ulrika F.S. D’Haenens-Johansson et al., “Large color- neodymium-doped yttrium orthovanadate, which is com-
less HPHT-grown synthetic gem diamonds from New Dia- monly used in laser applications. It can also form naturally
mond Technology, Russia,” Fall 2015 G&G, pp. 260–279). as the mineral wakefieldite-(Y), with an ideal chemical for-
Considering the HPHT growth method, the long-lasting mula of YVO4. His first observation was a striking color
greenish blue phosphorescence produced by exposure to change from pink or purple to a blue or even green color
SWUV and deep UV was expected. It was previously sug- under various lighting conditions and viewing angles. The
gested to be related to nitrogen-boron donor-acceptor pair finished gemstone (figures 89 and 90) displayed strong fire
recombination (Watanabe et al., 1997). However, the or- due to the material’s very high dispersion.
ange phosphorescence demonstrated a new stimulation Wakefieldite is a rare tetragonal mineral belonging to
source. Its combination with the greenish blue phospho- the xenotime mineral family with an ideal general formula
rescence and the identified visible-light excitation wave- of (REE)VO4, where REE = Y, La, Ce, and Nd among other
rare earth elements. Its general physical and optical prop- examples of faceted wakefieldite. In fact, this was the first
erties include a hardness of 5, specific gravity of 4.25, uni- faceted synthetic wakefieldite seen in a GIA laboratory.
axial + optic sign with refractive indices of nω = 2.000 and Chemistry and visible absorption spectra were collected to
nε = 2.140, birefringence of 0.140, and dispersion of 0.084. quantitatively study the striking color-change behavior.
With prominent, perfect cleavage and relatively low hard- A polished wafer with 10.6 mm thickness was analyzed.
ness, the material is difficult to polish. Natural wakefield- Laser ablation–inductively coupled plasma–mass spectrom-
ite occurs as very small, non-gem crystals unsuitable for etry revealed the material was composed of mostly yttrium
faceting; Czochralski-pulled materials represent the only and vanadium, with 2.2% neodymium by weight (0.03 per
2.5
610 60
2.0 50
541
40
1.5
435
30
1.0
20
0.5
10
0 0
400 450 500 550 600 650 700
WAVELENGTH (nm)
Figure 91. The visible absorption spectra of neodymium-doped YVO4 are shown with the relative power distribution
curves of CIE illuminants F10 and D65 and an Eiko warm white fluorescent bulb with color temperature of 2800K.
formula unit). Since Y3+ does not produce color on its own, the color was determined by the transmission windows in
the color must be derived from the addition of Nd3+ ions sub- the spectrum (440–460, 490–500, 550–570, and 620–670
stituting for Y3+ ions in the crystal lattice. Figure 91 shows nm), which remain constant when switching between these
polarized absorption spectra in the visible range collected illuminants. This was confirmed by observation of the
with an ultraviolet/visible/near-infrared spectrometer for stone in outdoor conditions, which produced the same
both the ordinary ray (o-ray) and extraordinary ray (e-ray). The pinkish purple color seen in incandescent light. The use of
expected color was calculated from the absorption spectra warm fluorescent light (Eiko fluorescent light in figures 91
based on the formula described by Z. Sun et al. (“Quantitative and 92) with color temperature of 2800K also reproduced
definition of strength of chromophores in gemstones and the the greenish blue to blue color seen in cool fluorescent light
impact on color change in pyralspite garnets,” Color Research (F10). It is also worth noting that the absorption features of
and Application, Vol. 47, No. 5, 2022, pp. 1134–1154). Nd3+ ions at 541 and 610 nm were strongly dependent on
As shown in figure 92, the material exhibited a general the polarization of the light, resulting in a strong pleochro-
pink to purple to violet color in most illuminants except ism (grayish purple for the o-ray and green-blue for the e-
the Eiko warm fluorescent light and the o-ray of CIE stan- ray), only observed under F10 illuminant (figure 92).
dard illuminant F10, which represents a typical cool fluo- The color panels under two LED illuminants in GIA’s
rescent light. In fact, the color-change behavior noticed by standard viewing box were also calculated in figure 92. The
author AA could be replicated when comparing illuminant two LED lights, warm and cool, closely imitate the CIE
F10 to any of the other illuminants such as daylight or in- standard illuminants A and D65. The two sets of color pan-
candescent light. Switching between warm incandescent els (A = LED warm pair and D65 = LED cool pair) are ex-
light and actual cool daylight did not produce a dramatic tremely close to each other based on their L, C, and H
change of color. The emission spectrum of F10 fluorescent (lightness, chroma, and hue) color coordinates. This study
also illustrates the consistent results of GIA’s standard
light is mainly composed of sharp peaks at 435, 545, and
viewing box in grading gemstone color.
610 nm (figure 91). Therefore, the color of the synthetic
wakefieldite crystal under illuminant F10 is only deter- Ziyin Sun, Shiyun Jin, Adriana Gudino, and
mined by the small absorption features at ~435, 541, and Aaron C. Palke
610 nm of the Nd3+ ions. Broadband emitters such as incan- Carlsbad, California
descent light and actual daylight (D65 in figure 91), on the Arya A. Akhavan
other hand, do not have these sharp emission features, so Surgical Precision Gems, Toronto
E ll c
E﬩c
Figure 92. Color panels of the 10.59 mm wafer in six different lighting conditions were calculated for both the o-
ray and e-ray. In the top row, A and D65 are CIE standard illuminants for incandescent light and daylight. Eiko is
a fluorescent bulb with color temperature of 2800K, while F10 is a CIE standard narrowband fluorescent illumi-
nant. Warm (2700K) and cool (6700K) LEDs represent the illuminants in the GIA standard viewing box.
Figure 95. Unaltered tubes in the heated purplish Chromophore behaviors (including the 880 nm absorption
pink sapphire. Photomicrograph by Ugo Hennebois; band) in an irradiated pink sapphire. Irradiation is a known
field of view 2 mm. process for enhancing color in corundum, particularly yel-
low and pink sapphire. Recently, some rubies and pink sap-
phires with bluish tint were reportedly treated with
radiation (“LMHC makes progress on laboratory report har-
monisation, discussed current challenges in detection of
corundum treatments,” LMHC press release, March 14,
2023). However, chromophore behaviors in irradiated
ruby/pink sapphire have not been fully investigated. This
report shows preliminary results of an experiment involving
irradiated pink sapphire. An untreated Madagascar pink sap-
phire with a blue modifier (figure 96) was fabricated as an
optical wafer with two polished faces perpendicular to the
c-axis for ultraviolet/visible/near-infrared (UV-Vis-NIR)
spectroscopic study. Trace element chemistry was analyzed
in the UV-Vis-NIR measurement area using laser
ablation−inductively coupled plasma−mass spectrometry.
This information can be used to link the visual color and
the color-causing trace elements listed in figure 96.
The spectrum of the untreated sample displayed broad
absorption bands at ~400 and ~560 nm together with weak
peaks at ~470 and at 693 nm, demonstrating that the Cr3+
chromophore was responsible for the pink color (blue line
in figure 97; see E.V. Dubinsky et al., “A quantitative de-
Elements Mg Ti V Cr Fe Ga
Concentration
30 ± 7a 21 ± 4 16 ± 1 137 ± 7 480 ± 27 15 ± 1
(ppma)
Detection limits
0.05 0.14 0.01 0.17 2.2 0.01
(ppma)
a
average ± standard deviation
Figure 96. Color-calibrated photo of a 0.664 ct pink sapphire from Madagascar before and after irradiation, and
after fade test using fiber-optic light for 6 hours. Path length/thickness: 1.514 mm. Photos by Sasithorn Engniwat.
scription of the causes of color in corundum,” Spring 2020 For our radiation experiment, the sample was treated
G&G, pp. 2–28). This sample also showed a weak broad with a gamma irradiation dose of 500 kGy at the Irradia-
band at around 580 nm related to Fe2+-Ti4+ pairs, which pro- tion Center at the Thailand Institute of Nuclear Technol-
duced a blue color, modifying the pink color from Cr3+ to ogy (public organization). After irradiation, the pink
purple-pink. Weak Fe3+-related absorption features were sapphire changed to a padparadscha-like coloration in
also observed, represented by a broad band at ~330 nm and which the subtle blue color was partially removed (figure
narrow peaks at 377, 388, and 450 nm. The iron-related 96). The UV-Vis-NIR spectrum after irradiation showed a
chromophore only causes significant yellow color at rela- significant increase in absorption intensities at wave-
tively high iron concentrations (greater than ~1000 ppma) lengths shorter than ~560 nm or longer than ~660 nm (red
due to Fe3+ chromophores’ weak color strength. line in figure 97). To observe changes in chromophore be-
UV-VIS-NIR SPECTRA
8.5
Before irradiation
7.5 Figure 97. Polarized
ABSORPTION COEFFICIENT (cm–1)
After irradiation
Difference spectrum UV-Vis-NIR spectra
6.5
comparisons of the pink
5.5 Cr 3+ sapphire before and
Cr 3+
410
560 after irradiation with a
4.5 gamma irradiation dose
of 500 kGy. The differ-
3.5
ence spectrum revealed
2.5 a significant increase in
Cr 3+
Trapped hole-Cr 3+ 693 880 trapped hole paired
1.5 ~470
with Cr3+ and the 880
Fe 2+-Ti4+ nm band in the irradi-
0.5 580
0 ated pink sapphire.
-0.5
300 400 500 600 700 800 900 1000 1100
WAVELENGTH (nm)
havior caused by irradiation, the spectrum after irradiation that has been heat treated, such as heated Madagascar sap-
was subtracted from the pretreatment spectrum. The dif- phire (E.B. Hughes and R. Perkins, “Madagascar sapphire:
ference spectrum (green line in figure 97) revealed that this Low-temperature heat treatment experiments,” Summer
acceptor-dominated corundum with an atomic concentra- 2019 G&G, pp. 184–197) or heated Rock Creek sapphire
tion of magnesium greater than the sum of titanium and (J.L. Emmett and T.R. Douthit, “Heat treating the sap-
silicon concentrations created a strong absorption feature phires of Rock Creek, Montana,” Winter 1993 G&G, pp.
below ~560 nm to the UV region, which matches well 250–272). This feature can also be found in Mozambican
with the trapped hole associated with the Cr3+ spectrum ruby after heat treatment (S. Saeseaw et al., “Update on
for causing orange coloration (Dubinsky et al., 2020). “low-temperature” heat treatment of Mozambican ruby:
Using the absorption cross section information provided A focus on inclusions and FTIR spectroscopy,” GIA Re-
in Dubinsky et al. (2020), the concentration of trapped search News, April 30, 2018). The origin of this band is not
hole-Cr3+ chromophores induced by irradiation was ap- fully understood but may be related to iron clusters.
proximately 0.8 ppma in the sample. This chromophore The 880 nm band was absent in the UV-Vis-NIR spec-
had very high color strength, and therefore a noticeable trum of this sample before treatment. Interestingly, this
color change could be observed with only a tiny concen- pink sapphire developed the 880 nm band after irradiation,
tration of the trapped hole paired with Cr3+ created after with a significant intensity around 1.2 cm–1. Color stability
treatment. The Fe2+-Ti4+ chromophore also reduced by ap- testing is usually performed in gem laboratories for yellow
proximately 0.7 ppma in the treated sample, resulting in to padparadscha sapphires that may contain unstable color
less blue color modification. This slight lightening in blue centers (e.g., A.C. Palke et al., “An update on sapphires
color after irradiation is possibly due to the change in ox- with unstable color,” GIA Research News, December 12,
idation state of iron (which would reduce the number of 2022; Summer 2022 GNI, pp. 259–260). After the color sta-
Fe2+-Ti4+ pairs). In addition, the creation of orange color bility test (figures 96 and 98), the orange coloration intro-
(trapped hole-Cr3+) masked a certain portion of remaining duced by irradiation faded away after exposure to intense
blue color after treatment, as blue and orange are comple- incandescent light due to the dissociation of the trapped
mentary colors. The change in UV-Vis-NIR spectrum cor- hole paired with Cr3+, whereas the 880 nm band remained.
responded with the change in color appearance caused by This preliminary observation suggests that the 880 nm
irradiation. band can be produced by an irradiation process, and this
When studying absorption features in the UV-Vis-NIR feature could provide some interesting evidence of treat-
spectrum of corundum, a broad band centered at around ment, either heat or irradiation, in pink sapphires and ru-
880 nm in the red to near-infrared region is typically asso- bies. However, further studies would be needed to
ciated with basalt-related blue sapphire (e.g., A.C. Palke et understand the development of the 880 nm absorption
al., “Geographic origin determination of blue sapphire,” band.
Winter 2019 G&G, pp. 536–579). This band has little or no Wasura Soonthorntantikul and Wim Vertriest
impact on color. In addition to basalt-related blue sapphires GIA, Bangkok
that are exposed to heat naturally, the 880 nm band can be Aaron Palke
induced in the spectrum of a metamorphic-type sapphire GIA, Carlsbad
The distinctive morphological features of Colombian emeralds, such as their complex growth patterns, conical shapes, and inclusion characteristics, significantly impact their commercial appeal. These features not only contribute to the emerald's unique visual aesthetics but also to its rarity and collector's interest. The formation mechanisms, leading to intriguing patterns like 'gota de aceite' or the trapiche effect, enhance their desirability. Consequently, emeralds displaying these natural occurrences often command higher values in the marketplace, being perceived as more authentic and representative of the Colombian origin, thus heightening their allure among gem enthusiasts and investors .
Emerald crystal growth is characterized by features such as growth planes parallel to external faces, often resulting in prismatic to columnar habits. Key growth morphology includes layers formed during multi-step processes, with some crystals showing characteristics like etching and dissolution features, resulting in pits, grooves, and hillocks on the surface . These features, including skeletal growth and polygonal overgrowth, contribute to unique internal structures like cups or conical shapes, affecting crystal clarity and gemstone quality . Variations in growth conditions, such as mineral inclusions or environmental changes, can lead to nonuniform growth, impacting aesthetics and value. For instance, emeralds with skeletal or incomplete growth may show remarkable but less desirable aesthetic features like cavities or distinct zoning patterns, influencing their suitability as gemstones .
Challenges in identifying atypical bead cultured pearls stem from the use of various nuclei which blur the lines between natural and cultured pearls. For instance, using lower-quality pearls as bead nuclei is common, but it complicates the detection of these pearls as distinct from natural ones. Techniques like X-ray computed microtomography (μ-CT) and real-time microradiography (RTX) have enhanced the ability to discern features such as the demarcation line between bead nuclei and nacre layers . Atypical bead cultured pearls (aBCPs) often involve complex internal structures, such as non-bead pearls used as nuclei, which can include distinct organic features and growth arcs visible via imaging techniques . Advancements include utilizing spectral analytics like ultraviolet/visible reflectance and photoluminescence spectroscopy to analyze pigmentation and structural composition, which help differentiate between naturally and artificially colored pearls . Despite these advancements, the presence of atypical nuclei, such as heart-shaped or non-traditional forms, presents a significant challenge, prompting the continuous development of more sophisticated identification methods .
The primary properties of Montana sapphires include a broad color range, with hues such as blue, green, yellow, orange, purple, and pink, commonly found in secondary deposits like Rock Creek, Missouri River, and Dry Cottonwood Creek . These sapphires often necessitate enhancement techniques to increase their appeal in the gem and jewelry market. The most prevalent enhancement technique is high-temperature heat treatment, which is applied to improve or intensify their color, making them more desirable for use in jewelry . This process involves the use of specialized resistance-style furnaces that allow careful control of temperature and oxidation environments . These treatments are typically applied due to the unique chemical makeup of Montana sapphires, requiring specific treatment conditions . Additionally, the heat treatment technology, originally developed in the 1990s, has notably improved the economics of mining Montana sapphires by significantly enhancing their color and clarity .
Inclusions within Montana sapphires, such as specific kinds of rutile silk, mica, and unique multiphase inclusions, assist in determining their geographic origin. By comparing these inclusion features with those from other regions, gemologists can separate Montana sapphires from similar-looking stones from Tanzania's Umba and Songea regions. Additionally, trace element chemistry, which varies by geographic origin, further helps in identifying and confirming the primary source of a gemstone .
Trapiche emeralds exhibit a distinct pattern characterized by opaque black arms or spokes radiating from a central core that divide the crystal into separate sectors, often resembling a wheel or star shape. These features typically form due to the presence of mineral inclusions acting as obstacles during growth, causing incomplete and nonuniform growth in trapiche emeralds . The growth and dissolution processes involve polygonal growth of small columnar emerald crystals within the "cups" or cavities, followed by subsequent overgrowth on these formations . Additionally, etching processes, involving aggressive dissolution fluids, create unique textural features such as indentations, hillocks, and cavities on the crystal surfaces, which may contribute to the trapiche effect .
Optical and X-ray topography are used in studying gemstone growth to evaluate the internal structures and morphological features resulting from complex growth processes like those observed in Colombian emeralds . These techniques are instrumental in identifying growth zones within gems, revealing structural inclusions, etching patterns, and the degree of skeletal growth and dissolution which are not readily visible otherwise. This is particularly crucial for understanding the growth stages and environmental conditions that lead to distinct gem characteristics such as color zoning and crystal habit variations . By applying these techniques, researchers can distinguish between natural growth and post-growth environmental influences, aiding in the understanding of gemological properties and the geological history of gemstone formation .
Recent developments in Montana sapphire mining have significantly enhanced their market presence and influenced consumer preferences through increased production, marketing efforts, and technological advances. Potentate Mining and other stakeholders have aggressively marketed Montana sapphires domestically and internationally, utilizing social media to boost their profile . The emphasis on transparency and traceability within the jewelry industry has also made these sapphires more appealing to consumers, aligning with trends favoring ethically sourced gems . Technological advances such as high-temperature heat treatment have improved the color and clarity of these sapphires, making them more desirable in the gem market . With large reserves still available and efficient mining operations, Montana sapphires' diverse color range continues to appeal to a broad spectrum of jewelry styles, further solidifying their growing market presence . The combination of increased production, aggressive marketing, and enhanced gem quality has positioned Montana sapphires as a significant player in both domestic and international markets.
Trace element chemistry plays a crucial role in determining gemstone provenance by revealing unique geochemical signatures associated with specific geographic locations. For example, Montana sapphires are identifiable by distinctive trace element profiles, including variations in the concentrations of elements like iron, titanium, and magnesium, derived from laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) trace element measurements . Similarly, trace element chemistry was used to analyze Liberian rubies, which showed specific levels of iron, chromium, gallium, and vanadium, helping to ascertain the geological origin of these stones and providing potential new sources of income for local communities . This analytical approach supports transparency and traceability in the gemstone supply chain by linking specific chemical compositions to their geographic sources .
Provenance Proof Blockchain is used to track gemstones, ensuring transparency and traceability in the supply chain. This system allows each gemstone's journey to be documented and verified, enhancing trust and accountability in the mining and trading processes . Additionally, Virtu Gem has implemented the CRAFT Code to improve safety, labor conditions, and environmental planning at mining sites, further supporting transparency in the supply chain . These efforts are part of a broader movement to promote ethical and sustainable practices in the gemstone industry.