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Tourmaline
Tourmaline
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Tourmaline
A stone cut open and polished, revealing a bright rainbow of colors
General
CategoryCyclosilicate
Formula(Ca,K,Na, )(Al,Fe,Li,Mg,Mn)3(Al,Cr,Fe,V)6
(BO3)3(Si,Al,B)6O18(OH,F)4
[1][2]
IMA symbolTur[3]
Crystal systemTrigonal
Crystal classDitrigonal pyramidal (3m)
H-M symbol: (3m)
Space groupR3m (no. 160)
Identification
ColorMost commonly black, but can range from colorless to brown, red, orange, yellow, green, blue, violet, pink, or hues in-between. It can also be bi-colored, or even tri-colored. Rarely, it can be found as neon green or electric blue.
Crystal habitParallel and elongated; acicular prisms, sometimes radiating; massive; scattered grains (in granite)
CleavageIndistinct
FractureUneven, small conchoidal
TenacityBrittle
Mohs scale hardness7.0–7.5
LusterVitreous, sometimes resinous
StreakWhite
DiaphaneityTranslucent to opaque
Specific gravity3.06+0.20–0.06[1]
Density2.82–3.32
Polish lusterVitreous[1]
Optical propertiesDouble-refractive, uniaxial negative[1]
Refractive indexnω = 1.635–1.675
nε = 1.610–1.650
Birefringence−0.018 to −0.040; typically about −0.020 but in dark stones it may reach −0.040[1]
Pleochroism
  • Typically moderate to strong[1]
  • Red: definite; dark red, light red
  • Green: strong; dark green, yellow-green
  • Brown: definite; dark brown, light brown
  • Blue: strong; dark blue, light blue
Dispersion0.017[1]
Ultraviolet fluorescencePink stones; inert to very weak red to violet in long and short wave[1]
Absorption spectraStrong narrow band at 498 nm, and almost complete absorption of red down to 640 nm in blue and green stones; red and pink stones show lines at 458 and 451 nm, as well as a broad band in the green spectrum[1]
Main tourmaline producing countries

Tourmaline (/ˈtʊərməlɪn, -ˌln/ TOOR-mə-lin, -⁠leen) is a crystalline silicate mineral group in which boron is compounded with elements such as aluminium, iron, magnesium, sodium, lithium, or potassium. This gemstone comes in a wide variety of colors.

The name is derived from the Sinhalese tōramalli (ටෝරමල්ලි), which refers to the carnelian gemstones.[4]

History

[edit]

Brightly colored Ceylonese gem tourmalines were brought to Europe in great quantities by the Dutch East India Company to satisfy a demand for curiosities and gems. Tourmaline was sometimes called the "Ceylonese Magnet" because it could attract and then repel hot ashes due to its pyroelectric properties.[5]

Tourmalines were used by chemists in the 19th century to polarize light by shining rays onto a cut and polished surface of the gem.[6]

Species and varieties

[edit]

Commonly encountered species and varieties of tourmaline include the following:

  • Schorl species
    • Brownish-black to black—schorl
  • Dravite species (from the Drave district of Carinthia)
    • Dark yellow to brownish-black—dravite
  • Elbaite species (named after the island of Elba, Italy)
    • Red or pinkish-red—rubellite variety
    • Light blue to bluish-green—indicolite variety (from indigo)
    • Green—verdelite variety
    • Colorless—achroite variety (from Ancient Greek άχρωμος (ákhrōmos) 'colorless')

Schorl

[edit]
A single stark green fluorite isolated on top of schorl crystals
Schorl, magnified 10×

The most common species of tourmaline is schorl, the sodium iron (divalent) endmember of the group. It may account for 95% or more of all tourmaline in nature. The early history of the mineral schorl shows that the name "schorl" was in use prior to 1400 because a village known today as Zschorlau (in Saxony, Germany) was then named "Schorl" (or minor variants of this name), and the village had a nearby tin mine where, in addition to cassiterite, black tourmaline was found. The first description of schorl with the name "schürl" and its occurrence (various tin mines in the Ore Mountains) was written by Johannes Mathesius (1504–1565) in 1562 under the title "Sarepta oder Bergpostill".[7] Up to about 1600, additional names used in the German language were "Schurel", "Schörle", and "Schurl". Beginning in the 18th century, the name Schörl was mainly used in the German-speaking area. In English, the names shorl and shirl were used in the 18th century. In the 19th century the names common schorl, schörl, schorl and iron tourmaline were the English words used for this mineral.[7]

Dravite

[edit]
Black dravite on a grey matrix

Dravite, also called brown tourmaline, is the sodium magnesium rich tourmaline endmember. Uvite, in comparison, is a calcium magnesium tourmaline. Dravite forms multiple series, with other tourmaline members, including schorl and elbaite.[8]

The name dravite was used for the first time by Gustav Tschermak (1836–1927), Professor of Mineralogy and Petrography at the University of Vienna, in his book Lehrbuch der Mineralogie (published in 1884) for magnesium-rich (and sodium-rich) tourmaline from village Dobrova near Unterdrauburg in the Drava river area, Carinthia, Austro-Hungarian Empire. Today this tourmaline locality (type locality for dravite) at Dobrova (near Dravograd), is a part of the Republic of Slovenia.[9] Tschermak gave this tourmaline the name dravite, for the Drava river area, which is the district along the Drava River (in German: Drau, in Latin: Drave) in Austria and Slovenia. The chemical composition which was given by Tschermak in 1884 for this dravite approximately corresponds to the formula NaMg3(Al,Mg)6B3Si6O27(OH), which is in good agreement (except for the OH content) with the endmember formula of dravite as known today.[9]

Dravite varieties include the deep green chromium dravite and the vanadium dravite.[10]

Elbaite

[edit]
Elbaite with quartz and lepidolite on cleavelandite

A lithium-tourmaline elbaite was one of three pegmatitic minerals from Utö, Sweden, in which the new alkali element lithium (Li) was determined in 1818 by Johan August Arfwedson for the first time.[11] Elba Island, Italy, was one of the first localities where colored and colorless Li-tourmalines were extensively chemically analysed. In 1850, Karl Friedrich August Rammelsberg described fluorine (F) in tourmaline for the first time. In 1870, he proved that all varieties of tourmaline contain chemically bound water. In 1889, Scharitzer proposed the substitution of (OH) by F in red Li-tourmaline from Sušice, Czech Republic. In 1914, Vladimir Vernadsky proposed the name Elbait for lithium-, sodium-, and aluminum-rich tourmaline from Elba Island, Italy, with the simplified formula (Li,Na)HAl6B2Si4O21.[11] Most likely the type material for elbaite was found at Fonte del Prete, San Piero in Campo, Campo nell'Elba, Elba Island, Province of Livorno, Tuscany, Italy.[11] In 1933 Winchell published an updated formula for elbaite, H8Na2Li3Al3B6Al12Si12O62, which is commonly used to date written as Na(Li1.5Al1.5)Al6(BO3)3[Si6O18](OH)3(OH).[11] The first crystal structure determination of a Li-rich tourmaline was published in 1972 by Donnay and Barton, performed on a pink elbaite from San Diego County, California, United States.[citation needed]

Chemical composition

[edit]
Elbaite

The tourmaline mineral group is chemically one of the most complicated groups of silicate minerals. Its composition varies widely because of isomorphous replacement (solid solution), and its general formula can be written as XY3Z6(T6O18)(BO3)3V3W, where:[12]

The 41 minerals in the group (endmember formulas) recognized by the International Mineralogical Association
Species Name Ideal Endmember Formula IMA Number Symbol
Adachiite CaFe2+3Al6(Si5AlO18)(BO3)3(OH)3OH 2012-101 Adc
Alumino-oxy-rossmanite ▢Al3Al6(Si5AlO18)(BO3)3(OH)3O 2020-008 Aorsm
Bosiite NaFe3+3(Al4Mg2)Si6O18(BO3)3(OH)3O 2014-094 Bos
Celleriite ▢(Mn2+2Al)Al6(Si6O18)(BO3)3(OH)3(OH) 2019-089 Cll
Chromium-dravite NaMg3Cr6Si6O18(BO3)3(OH)3OH 1982-055 Cdrv
Chromo-alumino-povondraite NaCr3(Al4Mg2)Si6O18(BO3)3(OH)3O 2013-089 Capov
Darrellhenryite NaLiAl2Al6Si6O18(BO3)3(OH)3O 2012-026 Dhry
Dravite NaMg3Al6Si6O18(BO3)3(OH)3OH - 1884 - Drv
Dutrowite Na(Fe2.5Ti0.5)Al6Si6O18(BO3)3(OH)3O 2019-082 Dtw
Elbaite Na(Li1.5,Al1.5)Al6Si6O18(BO3)3(OH)3OH - 1913 - Elb
Ertlite NaAl3Al6(Si4B2O18)(BO3)3(OH)3O 2023-086 Etl
Ferro-bosiite NaFe3+3(Al4Fe2+2)Si6O18(BO3)3(OH)3O 2022-069 Fbos
Feruvite CaFe2+3(MgAl5)Si6O18(BO3)3(OH)3OH 1987-057 Fer
Fluor-buergerite NaFe3+3Al6Si6O18(BO3)3O3F 1965-005 Fbu
Fluor-dravite NaMg3Al6Si6O18(BO3)3(OH)3F 2009-089 Fdrv
Fluor-elbaite Na(Li1.5,Al1.5)Al6Si6O18(BO3)3(OH)3F 2011-071 Felb
Fluor-liddicoatite Ca(Li2,Al)Al6Si6O18(BO3)3(OH)3F 1976-041[a] Fld
Fluor-rossmanite ▢(LiAl2)Al6Si6O18(BO3)3(OH)3F 2023-111 Frsm
Fluor-schorl NaFe2+3Al6Si6O18(BO3)3(OH)3F 2010-067 Fsrl
Fluor-tsilaisite NaMn2+3Al6Si6O18(BO3)3(OH)3F 2012-044 Ftl
Fluor-uvite CaMg3(Al5Mg)Si6O18(BO3)3(OH)3F - 1930 - Fluvt
Foitite ▢(Fe2+2Al)Al6Si6O18(BO3)3(OH)3OH 1992-034 Foi
Lucchesiite Ca(Fe2+)3Al6Si6O18(BO3)3(OH)3O 2015-043 Lcc
Magnesio-dutrowite Na(Mg2.5Ti0.5)Al6Si6O18(BO3)3(OH)3O 2023-015 Mdtw
Magnesio-foitite ▢(Mg2Al)Al6Si6O18(BO3)3(OH)3OH 1998-037 Mfoi
Magnesio-lucchesite Ca(Mg3Al6Si6O18(BO3)3(OH)3O 2019-025 Mlcc
Maruyamaite K(MgAl2)(Al5Mg)Si6O18(BO3)3(OH)3O 2013-123 Mry
Olenite NaAl3Al6Si6O18(BO3)3O3OH 1985-006 Ole
Oxy-chromium-dravite NaCr3(Mg2Cr4)Si6O18(BO3)3(OH)3O 2011-097 Ocdrv
Oxy-dravite Na(Al2Mg)(Al5Mg)Si6O18(BO3)3(OH)3O 2012-004 Odrv
Oxy-foitite ▢(Fe2+Al2)Al6Si6O18(BO3)3(OH)3O 2016-069 Ofoi
Oxy-schorl Na(Fe2+2Al)Al6Si6O18(BO3)3(OH)3O 2011-011 Osrl
Oxy-vanadium-dravite NaV3(V4Mg2)Si6O18(BO3)3(OH)3O 1999-050 Ovdrv
Povondraite NaFe3+3(Fe3+4Mg2)Si6O18(BO3)3(OH)3O 1979[b] Pov
Princivalleite Na(Mn2Al)Al6Si6O18(BO3)3(OH)3O 2020-056 Pva
Rossmanite ▢(LiAl2)Al6Si6O18(BO3)3(OH)3OH 1996-018 Rsm
Schorl NaFe2+3Al6Si6O18(BO3)3(OH)3OH - 1505 - Srl
Tsilaisite NaMn2+3Al6Si6O18(BO3)3(OH)3OH 2011-047 Tsl
Uvite CaMg3(Al5Mg)Si6O18(BO3)3(OH)3OH 2000-030 Uvt
Vanadio-oxy-chromium-dravite NaV3(Cr4Mg2)Si6O18(BO3)3(OH)3O 2012-034 Vocdrv
Vanadio-oxy-dravite NaV3(Al4Mg2)Si6O18(BO3)3(OH)3O 2012-074 Vodrv
  1. ^ Named 'liddicoatite' in 1976; renamed to fluor-liddicoatite by the IMA in 2011
  2. ^ Named 'ferridravite' in 1979; renamed to povondraite by the IMA in 1990

Mineral species that were named before the IMA was founded in 1958 do not have an IMA number.

The IMA commission on new mineral names published a list of approved symbols for each mineral species in 2021.[13]

A revised nomenclature for the tourmaline group was published in 2011.[14][15][16]

Physical properties

[edit]

Crystal structure

[edit]
Tri-chromatic elbaite crystals on quartz, Himalaya Mine, San Diego Co., California, US

Tourmaline is a six-member ring cyclosilicate having a trigonal crystal system. It occurs as long, slender to thick prismatic and columnar crystals that are usually triangular in cross-section, often with curved striated faces. The style of termination at the ends of crystals is sometimes asymmetrical, called hemimorphism. Small slender prismatic crystals are common in a fine-grained granite called aplite, often forming radial daisy-like patterns. Tourmaline is distinguished by its three-sided prisms; no other common mineral has three sides. Prisms faces often have heavy vertical striations that produce a rounded triangular effect. Tourmaline is rarely perfectly euhedral. An exception was the fine dravite tourmalines of Yinnietharra, in western Australia. The deposit was discovered in the 1970s, but is now exhausted. All hemimorphic crystals are piezoelectric, and are often pyroelectric as well.[citation needed]

A crystal of tourmaline is built up of units consisting of a six-member silica ring that binds above to a large cation, such as sodium. The ring binds below to a layer of metal ions and hydroxyls or halogens, which structurally resembles a fragment of kaolin. This in turn binds to three triangular borate ions. Units joined end to end form columns running the length of the crystal. Each column binds with two other columns offset one-third and two-thirds of the vertical length of a single unit to form bundles of three columns. Bundles are packed together to form the final crystal structure. Because the neighboring columns are offset, the basic structural unit is not a unit cell: The actual unit cell of this structure includes portions of several units belonging to adjacent columns.[17][18]

Color

[edit]
Two dark-green rectangular tourmaline stones and one oval tourmaline stone
Bi-chromatic tourmaline crystal, 0.8 inches (2 cm) long
Tourmaline mineral, approximately 10 cm (3.9 in) tall

Tourmaline has a variety of colors. Iron-rich tourmalines are usually black to bluish-black to deep brown, while magnesium-rich varieties are brown to yellow, and lithium-rich tourmalines are almost any color: blue, green, red, yellow, pink, etc. Rarely, it is colorless. Bi-colored and multicolored crystals are common, reflecting variations of fluid chemistry during crystallization. Crystals may be green at one end and pink at the other, or green on the outside and pink inside; this type is called watermelon tourmaline and is prized in jewelry. An excellent example of watermelon tourmaline jewelry is a brooch piece (1969, gold, watermelon tourmaline, diamonds) by Andrew Grima (British, b. Italy, 1921–2007), in the collection of Kimberly Klosterman and on display at the Cincinnati Art Museum.[19] Some forms of tourmaline are dichroic; they change color when viewed from different directions.[20]

The pink color of tourmalines from many localities is the result of prolonged natural irradiation. During their growth, these tourmaline crystals incorporated Mn2+ and were initially very pale. Due to natural gamma ray exposure from radioactive decay of 40K in their granitic environment, gradual formation of Mn3+ ions occurs, which is responsible for the deepening of the pink to red color.[21]

Magnetism

[edit]

Opaque black schorl and yellow tsilaisite are idiochromatic tourmaline species that have high magnetic susceptibilities due to high concentrations of iron and manganese respectively. Most gem-quality tourmalines are of the elbaite species. Elbaite tourmalines are allochromatic, deriving most of their color and magnetic susceptibility from schorl (which imparts iron) and tsilaisite (which imparts manganese).[citation needed]

Red and pink tourmalines have the lowest magnetic susceptibilities among the elbaites, while tourmalines with bright yellow, green and blue colors are the most magnetic elbaites. Dravite species such as green chromium dravite and brown dravite are diamagnetic. A handheld neodymium magnet can be used to identify or separate some types of tourmaline gems from others. For example, blue indicolite tourmaline is the only blue gemstone of any kind that will show a drag response when a neodymium magnet is applied. Any blue tourmaline that is diamagnetic can be identified as paraiba tourmaline colored by copper in contrast to magnetic blue tourmaline colored by iron.[22]

Treatments

[edit]

Some tourmaline gems, especially pink to red colored stones, are altered by heat treatment to improve their color. Overly dark red stones can be lightened by careful heat treatment. The pink color in manganese-containing near-colorless to pale pink stones can be greatly increased by irradiation with gamma-rays or electron beams. Irradiation is almost impossible to detect in tourmalines, and does not, currently, affect the value. Heavily included tourmalines, such as rubellite and Brazilian paraiba, are sometimes clarity-enhanced. A clarity-enhanced tourmaline (especially the paraiba variety) is worth much less than an untreated gem of equal clarity.[23]

Geology

[edit]
Video of tourmaline ore

Tourmaline is found in granite and granite pegmatites and in metamorphic rocks such as schist and marble. Schorl and lithium-rich tourmalines are usually found in granite and granite pegmatite. Magnesium-rich tourmalines, dravites, are generally restricted to schists and marble. Tourmaline is a durable mineral and can be found in minor amounts as grains in sandstone and conglomerate, and is part of the ZTR index for highly weathered sediments.[24]

Localities

[edit]

Gem and specimen tourmaline is mined chiefly in Brazil and many parts of Africa, including Tanzania, Nigeria, Kenya, Madagascar, Mozambique, Malawi, and Namibia. It is also mined in Asia, notably in Pakistan, Afghanistan, and Indonesia as well as in Sri Lanka and India,[25] where some placer deposit material suitable for gem use is found.

United States

[edit]

Some fine gems and specimen material have been produced in the United States, with the first discoveries in 1822, in the state of Maine. California became a large producer of tourmaline in the early 1900s. The Maine deposits tend to produce crystals in raspberry pink-red as well as minty greens. The California deposits are known for bright pinks, as well as bicolors. During the early 1900s, Maine and California were the world's largest producers of gem tourmalines. The Empress Dowager Cixi of China loved pink tourmaline and bought large quantities for gemstones and carvings from the then new Himalaya Mine, located in San Diego County, California.[26] It is not clear when the first tourmaline was found in California. Native Americans have used pink and green tourmaline as funeral gifts for centuries. The first documented case was in 1890 when Charles Russel Orcutt found pink tourmaline at what later became the Stewart Mine at Pala, California in San Diego County.[27]

Brazil

[edit]
Watermelon Tourmaline mineral on quartz matrix (crystal approximately 2 cm (0.79 in) wide at face)

Almost every color of tourmaline can be found in Brazil, especially in Minas Gerais and Bahia. The new type of tourmaline, which soon became known as paraiba tourmaline, came in blue and green. Brazilian paraiba tourmaline usually contains abundant inclusions. Much of the paraiba tourmaline from Brazil does not actually come from Paraíba, but the neighboring state of Rio Grande do Norte. Material from Rio Grande do Norte is often somewhat less intense in color, but many fine gems are found there. It was determined that the element copper was important in the coloration of the stone.[28]

A large bluish-green tourmaline from Paraiba, measuring 36.44 mm × 33.75 mm × 21.85 mm (1.43 in × 1.33 in × 0.86 in) and weighing 191.87 carats (1.3536 oz; 38.374 g), is the world's largest cut tourmaline.[29][30] Owned by Billionaire Business Enterprises,[29] it was presented in Montreal, Quebec, Canada, on 14 October 2009.[30]

Africa

[edit]
Paraiba tourmaline from Mozambique

In the late 1990s, copper-containing tourmaline was found in Nigeria. The material was generally paler and less saturated than the Brazilian materials, although the material generally was much less included. A more recent African discovery from Mozambique has also produced tourmaline colored by copper, similar to the Brazilian paraiba. The Mozambique paraiba material usually is more intensely colored than the Nigerian and Mozambique Paraiba tourmaline have similar colors to the Brazilian Paraiba, but the prices are relatively cheaper, better clarity and larger sizes. In recent years the pricing of these beautiful gemstones has increased significantly.[31]

Another highly valuable variety is chrome tourmaline, a rare type of dravite tourmaline from Tanzania. Chrome tourmaline is a rich green color due to the presence of chromium atoms in the crystal. Of the standard elbaite colors, blue indicolite gems are typically the most valuable,[32] followed by green verdelite and pink to red rubellite.[33]

See also

[edit]
  • Benjamin Wilson – experimented with the electrical properties of tourmaline

References

[edit]

Further reading

[edit]
[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Tourmaline is a complex group of trigonal borosilicate minerals belonging to the cyclosilicate class, characterized by a general of XY₃Z₆(T₆O₁₈)(BO₃)₃V₃W, where X, Y, Z, T, V, and W represent various cation and anion sites occupied by elements such as sodium, calcium, aluminum, iron, , magnesium, , , oxygen, and . This structural complexity allows for over 40 recognized species within the tourmaline supergroup, with standardized based on dominant occupants at key sites. Tourmaline exhibits a wide of colors—from black and green to pink, blue, and multicolored varieties—due to trace elements like iron, , , , and rarely , making it one of the most color-diverse materials. Physically, it features a Mohs of 7 to 7.5, a specific of 2.9 to 3.2, and a vitreous to resinous luster, with crystals typically forming elongated prisms or columns up to several meters long. Geologically, tourmaline primarily forms in boron-rich environments such as granitic pegmatites, metamorphic rocks like schists and marbles, and hydrothermal veins, with major deposits in countries including , , , and the (particularly and ). Its chemical variability serves as an indicator for tracing magmatic and metamorphic processes, reflecting the composition of the host rocks. Notable varieties include (lithium-rich, often multicolored gems like watermelon tourmaline), schorl (iron-rich black crystals), dravite (magnesium-rich brown), and the vivid copper-bearing tourmaline prized for its neon blue-green hues. Beyond its aesthetic appeal as a for and an eighth-anniversary gem, tourmaline is valued for industrial applications due to its piezoelectric and pyroelectric properties, which generate electric charges under mechanical stress or temperature changes—properties historically speculated to aid Viking navigation and modernly used in pressure gauges and .

History

Etymology and Early References

The name "tourmaline" derives from the Sinhalese term tūramali (or turamali), a generic word used in (then known as Ceylon) to describe multicolored pebbles, often resembling or other mixed gems, extracted from alluvial gem gravels. This term encompassed a variety of unidentified colored stones, including what are now recognized as tourmalines, and was applied broadly without distinguishing specific mineral species. Dutch traders, operating through the , first encountered these gems in Ceylon during the late 1600s and began importing them to in significant quantities by the early 1700s. Records from the company's activities in Ceylon document the shipment of parcels of these multicolored stones around 1703, often mistakenly identified as zircons or other known gems due to their similar appearance and the limited understanding of mineral diversity at the time. The confusion arose because the stones' vibrant hues and water-worn forms mimicked more familiar varieties like hyacinth zircon, leading to their inclusion in trade inventories without separate classification. The first scientific description of tourmaline, highlighting its notable pyroelectric properties, was provided by Swedish naturalist in 1747. Linnaeus named it lapis electrica (electric stone), observing that heating the crystal caused it to attract lightweight particles like ash or dust, a he linked to —marking an early recognition of its unique thermal behavior in European scientific literature. This account built on informal Dutch observations from pipe-cleaning applications but formalized the mineral's distinctive traits for broader study.

Historical Significance and Use

Tourmaline has been valued in ancient civilizations for its aesthetic qualities, often incorporated into jewelry despite frequent misidentification with more renowned gems. In , the stone was believed to acquire its vibrant colors by passing through a , and it was used in amulets and decorative objects for its supposed protective properties. In , black schorl tourmaline appeared in jewelry, such as a 3rd-century CE ring featuring a schorl intaglio depicting , highlighting its role in classical adornment. Similarly, in , tourmaline was employed in sculptures and jewelry, prized for its durability and color variety. During the Age of Exploration, Brazilian tourmaline entered European markets in the 1500s through Spanish conquistadors, who exported green specimens mistaken for emeralds, thereby introducing the gem to Western lapidaries under false pretenses. This confusion persisted until the 1800s, when mineralogists distinguished tourmaline as a unique species, though its multicolored forms had long been known in and traded via the . In the , tourmaline's pyroelectric properties—generating electric charges when heated or cooled—sparked scientific interest, with early experiments by Dutch gem cutters in the early 1700s observing the stone attracting ash, leading to name it "lapis electricus" in 1747. In Victorian England, black schorl gained popularity in mourning jewelry, symbolizing grief and loss amid the era's elaborate commemorative customs. Concurrently, discoveries during California's late 1870s to early 1880s activities uncovered significant tourmaline deposits in and Riverside Counties, boosting American interest and exports, particularly of pink varieties to .

Classification

Mineral Species

The tourmaline supergroup comprises trigonal borosilicates classified within the cyclosilicate group, distinguished by a complex ring structure consisting of six corner-sharing SiO₄ tetrahedra (T₆O₁₈) interlinked with three BO₃ triangular units, along with additional anionic sites occupied by OH, O, or F. The International Mineralogical Association (IMA) approves species nomenclature based on dominant-valence occupancy at the X (9-fold), Y (6-fold), and Z (6-fold octahedral) sites in the general formula XY₃Z₆(T₆O₁₈)(BO₃)₃V₃W, where T is primarily Si (with possible Al substitution), V₃ represents three OH⁻ groups, and W is OH⁻, O²⁻, or F⁻. As of 2025, the tourmaline supergroup includes more than 40 IMA-approved species, classified into alkali, calcic, X-site vacant, and oxy groups. This structural framework allows for extensive solid-solution series, but species are delineated by the prevailing cations, such as Na or Ca at X, and varying combinations of Li, Mg, Fe²⁺, Fe³⁺, Al, or other divalent/trivalent metals at Y and Z sites. Key end-members, representing common species, are defined by distinct cation dominance that facilitates basic mineral identification through chemical analysis or spectroscopy. Schorl, the iron-dominant alkali tourmaline, has the end-member formula NaFe₃Al₆(BO₃)₃Si₆O₁₈(OH)₄, where Fe²⁺ occupies the Y site, imparting typically black coloration and distinguishing it from magnesium-rich variants. Dravite, with Mg dominant at Y, features the formula NaMg₃Al₆(BO₃)₃Si₆O₁₈(OH)₄, often appearing brown and identified by its higher Mg/Fe ratio compared to schorl. Elbaite, lithium-bearing and gem-relevant, is Na(Li_{1.5}Al_{1.5})Al₆(BO₃)₃Si₆O₁₈(OH)₄, where partial Li substitution at Y enables vibrant colors due to trace elements. Uvite, a calcic species, is characterized by Ca at X and Mg at Y, with formula CaMg₃(Al₅Mg)Si₆O₁₈(BO₃)₃(OH)₄ (the F analog is fluor-uvite), differing from alkali species in its calcium content and frequent fluorine enrichment. Rossmanite, an X-site vacant tourmaline, has the end-member ◻(LiAl₂)Al₆Si₆O₁₈(BO₃)₃(OH)₄, notable for its alkali deficiency and Al dominance at Y. Olenite, an oxy variant, is NaAl₃Al₆Si₆O₁₈(BO₃)₃(OH)₃O, identified by oxygen at the W site and high Al content, leading to colorless to pale forms. These differences in dominant cations, particularly Fe²⁺ versus Mg at Y or Na versus Ca at X, underpin IMA classification and enable differentiation via electron microprobe or wet chemistry. Gem varieties used in jewelry are primarily derived from and schorl series members, showcasing color diversity from these species.

Gem Varieties

Tourmaline gem varieties are primarily drawn from the species, which dominates the market due to its vibrant colors and suitability for . These varieties are distinguished commercially and aesthetically by their dominant hues, with naming conventions based on perceived color saturation and tone rather than strict chemical distinctions. Rubellite refers to tourmalines exhibiting pink, red, purplish red, orangy red, or brownish red colors, typically with medium to dark tones and reasonable saturation; however, some experts exclude lighter shades from this category to preserve the term for more vivid examples. Indicolite denotes blue varieties, ranging from dark violetish blue to pure blue or greenish blue, often prized for their depth and clarity in jewelry settings. Verdelite describes intense green tourmalines, sometimes specified as chrome tourmaline when colored by , offering a lush, emerald-like appeal without the latter's typical inclusions. Watermelon tourmaline is a distinctive zoned variety featuring a or core surrounded by a green rind, reminiscent of the fruit's cross-section; it is usually cut as thin slices or cabochons to highlight the dramatic color banding. tourmaline stands out for its neon-like violetish blue, greenish blue, or blue hues, caused by impurities, making it one of the most sought-after varieties for its electric glow. Color is the primary value driver for Paraíba tourmaline, with clarity secondary. Inclusions are common and generally tolerated, eye-clean stones command a premium, but the price impact of inclusions is relatively minor compared to other gems. Eye-visible inclusions typically cause only slight value reductions, while heavy inclusions can reduce value more noticeably if they affect transparency. However, synthetics lack the matching glow intensity of this electric neon blue due to challenges in replicating the precise copper and manganese content. Rarity significantly influences value across these varieties, but tourmaline exemplifies extreme scarcity, discovered in 1989 in Brazil's state and initially yielding only small quantities from pockets. Subsequent sourcing has expanded to , , and other global localities; it is considered rarer than diamonds due to its extremely limited sources, primarily in Brazil's Paraíba region, with only limited additional finds in Mozambique and Nigeria. As a result, supply remains limited, driving prices for fine Brazilian specimens to $20,000–$50,000 per carat or higher due to demand in high-end jewelry. In contrast, and indicolite command premium values for deep, saturated colors, while verdelite and varieties are valued for their aesthetic uniqueness but are generally more accessible than .

Chemical Composition

Tourmaline belongs to the cyclosilicate class and is characterized by the general XY3Z6(T6O18)(BO3)3V3WXY_3Z_6(T_6O_{18})(BO_3)_3V_3W, where the letters represent distinct crystallographic sites occupied by various cations and anions.
  • X site: Typically occupied by Na⁺, Ca²⁺, K⁺, or vacancy (□).
  • Y site: Accommodates a mix of divalent and trivalent cations, including Li⁺, Mg²⁺, Fe²⁺, Mn²⁺, Al³⁺, Fe³⁺, Cr³⁺, V³⁺, and Ti⁴⁺.
  • Z site: Primarily Al³⁺, with possible Fe³⁺, Cr³⁺, V³⁺, or Mg²⁺.
  • T site: Dominated by Si⁴⁺, with minor substitutions by Al³⁺ or B³⁺.
  • B site: Exclusively B³⁺ in three isolated groups.
  • V site: OH⁻ or O²⁻.
  • W site: OH⁻, F⁻, or O²⁻.
This formula reflects the tourmaline supergroup's complexity, with over 30 recognized species defined by the dominant-valency rule at key sites, as per the International Mineralogical Association (IMA) revised in 2011 and updated through 2022. End-member compositions for major species include:
  • Schorl (alkali group, Fe-dominant): NaFe²⁺₃Al₆(Si₆O₁₈)(BO₃)₃(OH)₃(OH).
  • Dravite (alkali group, Mg-dominant): NaMg₃Al₆(Si₆O₁₈)(BO₃)₃(OH)₃(OH).
  • (alkali group, Li-dominant): Na(Li₁.₅Al₁.₅)Al₆(Si₆O₁₈)(BO₃)₃(OH)₃(OH).
  • Uvite (calcic group): CaMg₃(Al₅Mg)(Si₆O₁₈)(BO₃)₃(OH)₃(OH).
Compositional variations arise from substitutions at the Y, Z, and W sites, influenced by trace elements such as Mn, Cr, , and Cu, which contribute to the group's color diversity.

Physical Properties

Crystal Structure and Habit

Tourmaline belongs to the trigonal crystal system and crystallizes in the space group , forming a complex borosilicate framework. This structure is built from slightly distorted six-membered rings of silicate tetrahedra ([Si₆O₁₈]) arranged parallel to the (0001) plane, linked by isolated triangular [BO₃] units and, in some species, additional tetrahedral [BO₄] groups. The framework is further stabilized by chains of edge-sharing octahedra occupied by divalent and trivalent cations (such as Al, Fe, Mg), which twist into helical arrangements along the c-axis, creating a distinctive three-dimensional . Variations in cation occupancy at these sites can subtly affect structural stability without altering the overall symmetry. The most common crystal habit of tourmaline is prismatic, with elongated crystals displaying prominent longitudinal striations parallel to the c-axis due to the alternation of faces. These s often exhibit a triangular or hexagonal cross-section with rounded edges and are typically terminated by rhombohedral or pyramidal faces, resulting in hemimorphic growth. Less frequently, tourmaline occurs in massive, granular aggregates or as fibrous and radial clusters, particularly in hydrothermal environments where influence morphology. Tourmaline possesses a Mohs hardness of 7 to 7.5, rendering it suitable for use in jewelry, and a specific of 3.0 to 3.3, which varies with compositional differences across . Twinning is uncommon but can occur on {10-11} or {40-41} planes, leading to intergrowths that mimic parallel crystals. Fluid inclusions, often appearing as thread-like trichites, are prevalent and can reduce clarity in transparent specimens by trapping remnants of the formative fluids.

Optical and Color Properties

Tourmaline exhibits uniaxial negative optical character, with refractive indices typically ranging from nω = 1.635–1.675 (ordinary ray) and nε = 1.62–1.64 (extraordinary ray). The is moderate to strong, varying between 0.014 and 0.032, which contributes to its distinct double and aids in gem identification. These properties arise from the mineral's complex borosilicate structure, allowing light to split into two polarized rays that travel at different speeds through the . A hallmark of tourmaline's optics is its strong pleochroism, where the gem displays different colors depending on the orientation of light relative to the crystal's c-axis. In green varieties, such as verdolite, this manifests as shifts from yellow-green to blue-green when viewed along different directions, enhancing the stone's visual depth. Darker green and brown tourmalines show even more pronounced dichroism, with colors like dark green to olive green, while paler specimens exhibit weaker effects. This pleochroism is most evident in elongated crystals and cut gems, where the intensity along the length (c-axis) often appears deeper than perpendicular views. The wide color range in tourmaline stems primarily from trace transition metals and intervalence charge transfer mechanisms. Green and blue hues often result from Fe2+–Fe3+ intervalence charge transfer (IVCT), which absorbs light in the red region, while pink and red varieties derive their color from manganese (Mn3+). The vivid turquoise to neon blue of Paraíba-type tourmaline is attributed to copper (Cu2+), frequently combined with manganese for enhanced saturation. These chromophores interact with the crystal lattice, producing sector zoning and color variations during growth. In gem cutting and display, tourmaline's dichroism requires careful orientation to optimize color appearance and minimize unwanted "bow-tie" effects, where mixed hues appear in the center of faceted stones. Cutters typically align the table facet to the c-axis for balanced color in strongly pleochroic material, such as green tourmaline, to avoid overly dark views along the length. This strategic enhances brilliance and appeal, particularly in jewelry settings where viewing angles vary, ensuring the gem's vibrant tones are showcased effectively.

Electrical and Thermal Properties

Tourmaline exhibits , a property by which it generates an in response to temperature changes, with the polarity aligned along the c-axis of its trigonal . The pyroelectric effect in tourmaline was first recorded in by Johann Georg Schmidt, who noted that heated tourmaline could attract bits of ash. The pyroelectric coefficient in tourmaline varies with composition, typically ranging from 1 to 20 μC m⁻² K⁻¹ at , influenced by factors such as iron content in schorl or lithium in . In addition to , tourmaline displays , producing a voltage under mechanical stress due to its non-centrosymmetric crystal lattice. Piezoelectric coefficients for common tourmaline species at include d₃₃ values of 2.3 pC/N for , 1.9 pC/N for schorl, and 3.4 pC/N for dravite, with d₃₁ ranging from -1.9 to -2.3 pC/N across these varieties; these values are approximately 1.5 times higher than those of α-quartz. This property has historically supported applications in pressure sensors and early electromechanical devices, though modern uses favor synthetic materials with higher coefficients. Tourmaline's is highly anisotropic, reflecting its , with principal coefficients α₁₁ (perpendicular to the c-axis) around 3.5–3.9 × 10⁻⁶ K⁻¹ and α₃₃ (parallel to the c-axis) around 7.7–9.1 × 10⁻⁶ K⁻¹ at for schorl and . This directional variation arises from differences in atomic bonding along the axes and contributes to the mineral's stability in geological environments with temperature gradients. Furthermore, certain iron-poor tourmaline varieties, such as dravite with low Fe-Ti content, exhibit weak , resulting in a negative that repels magnetic fields weakly. While tourmaline generates small piezoelectric voltages (with coefficients around 1.9-3.4 pC/N), these are minimal and transient, producing only minor charges insufficient for meaningful biological or therapeutic effects in passive applications such as consumer products.

Geology and Formation

Occurrence and Paragenesis

Tourmaline primarily occurs in granitic pegmatites, where it forms as an accessory during the late stages of , as well as in metamorphic rocks such as schists and gneisses, and in hydrothermal veins associated with igneous intrusions. In pegmatites, tourmaline crystals can grow to large sizes, often zoning from schorl-rich cores to elbaite-rich rims due to evolving fluid compositions. Metamorphic occurrences are common in boron-enriched protoliths, where tourmaline stabilizes across a wide range of pressure-temperature conditions, serving as a petrogenetic indicator. Hydrothermal veins host fibrous or massive tourmaline, typically in association with late-stage fluid circulation in fractured host rocks. The paragenesis of tourmaline reflects its host environment and boron availability. In granitic pegmatites, it is commonly associated with , (especially ), and ( or ), forming pockets or graphic intergrowths that indicate fractional processes. In metamorphic rocks like schists and gneisses, tourmaline coexists with , , , and , particularly in pelitic assemblages where it incorporates from the . Dravite, a magnesium-rich variety, often forms in boron-rich metasedimentary rocks derived from evaporitic or marine sediments, associating with dolomite, , and in such settings. Hydrothermal vein parageneses include tourmaline with , sulfides, and , highlighting its role in metasomatic alteration. Tourmaline formation typically occurs at temperatures between 400°C and 700°C, spanning magmatic to subsolidus conditions where solubility in fluids or melts is sufficient for precipitation. sources are diverse but commonly derive from evaporites, such as marine -rich sediments leached during , or from volcanic and hydrothermal activity that mobilizes through fluid infiltration. These sources provide the essential component, with external fluids often introducing into otherwise depleted systems, influencing tourmaline composition and stability.

Major Geological Settings

Tourmaline is predominantly hosted in granitic s within orogenic belts, where late-stage magmatic differentiation in collisional settings facilitates boron enrichment and crystal growth. These environments, such as the Alpine-Himalayan chain, feature folded and metamorphosed rocks that provide the necessary volatile-rich fluids for pegmatite emplacement during mountain-building episodes spanning from the to recent times. Examples include lithium-rich pegmatites in the Black Hills of , where tourmaline varieties like form in association with beryl and . In these settings, tourmaline crystals can exceed one meter in length, reflecting low-viscosity melt flow in crustal fractures. Metamorphic tourmalinites represent another key setting, forming in contact zones between boron-bearing sediments and intrusive bodies or during regional in orogenic belts. These rocks, often schistose and enriched in boron from proximal evaporitic or marine sources, develop under low- to medium-grade conditions, with ultra-high-pressure variants documented in the Dora Maira massif () and Kokchetav massif (). Hydrothermal deposits linked to zones further contribute, particularly in blackwall metasomatic zones where tourmaline precipitates from boron-rich fluids interacting with ultramafic rocks, as seen in and eclogite terrains. Such settings record fluid evolution in ore provinces, including tin and associations. Sedimentary boron concentrations in evaporite basins host authigenic tourmaline, formed through diagenetic processes in hypersaline environments where is mobilized from volcanic or continental sources. Detrital tourmaline is also common in clastic sediments derived from eroded igneous and metamorphic terrains, accumulating in placer-like deposits. Findings since 2000 highlight mantle-derived tourmaline in kimberlitic and lamproitic , such as dravitic varieties in diamond-bearing breccias from the Alto Paranaíba Igneous Province (), indicating rapid ascent of volatile-rich melts from depths exceeding 150 km. These occurrences underscore tourmaline's stability under conditions, with schorl stable up to at least 3.5 GPa (approximately 100 km depth in cold zones) before breakdown at higher temperatures.

Localities and Mining

North and South America

Tourmaline deposits in are primarily associated with granitic pegmatites and porphyry systems, with the hosting some of the earliest and most historically significant sites for gem-quality material. Mount Mica in , , stands as America's first major gem pegmatite, where elbaite tourmaline was discovered in 1820 during initial operations that uncovered crystals amid disintegrated rock. This locality has produced exceptional green, pink, and bi-color elbaite specimens over nearly two centuries, with sporadic modern since 2004 yielding high-quality gems from miarolitic cavities. In , the Pala Mining District in San Diego County emerged as a key source of pink tourmaline in the late 1800s, with mines such as the Stewart Lithia, Pala Chief, and Tourmaline Queen producing vibrant rubellite and bi-color crystals prized for their clarity and hue. Between 1902 and 1910, these operations supplied over 120 tons of gem-quality pink tourmaline, much of it exported to imperial , though current output remains limited and intermittent due to depleted pockets. U.S. gem tourmaline production is small-scale today, contributing modestly to the nation's overall output valued at around $99 million in 2023. In , tourmaline occurrences are more common in northern within porphyry copper districts, where schorl and dravite form as accessory minerals in hydrothermal veins and breccias. The District features notable tourmaline in association with mineralization, as documented in geological surveys from the early , though gem-quality material is rare and production focuses on industrial uses rather than . Similarly, in , Territory hosts tourmaline in porphyry Cu-Au-Mo deposits like , where Fe- and Mg-rich varieties occur as prismatic grains and vein fillings, serving as exploration indicators for mineralization since the . Other prospects, such as Tsa da Glisza, contain tourmaline porphyroblasts in greenschist-facies rocks linked to emerald potential, but commercial gem extraction is minimal. Mexican and Canadian tourmaline exports are negligible in trade statistics, with combined U.S. imports from these countries accounting for less than 1% of relevant semi-precious stone inflows as of 2024. South America's tourmaline production is dominated by , particularly in the pegmatite-rich terrains of state, where diverse varieties including paraiba-type and muldoon () emerge from complex granitic intrusions. The Jequitinhonha Valley, encompassing areas like Virgem da Lapa and Coronel Murta, features prolific mines such as Manoel Mutuca and Barra de Salinas, yielding gem-quality and schorl in vibrant pinks, greens, and bi-colors from eluvial deposits. These sites contribute to ' status as 's leading gem province, responsible for 74% of national gemstone output as of the early . The iconic paraiba tourmaline, renowned for its neon blue-green hues due to content, was first discovered in 1989 by miner Heitor Dimas Barbosa—who passed away in 2023—at the Mina da Batalha in state (adjacent to influences), after years of prospecting manganotantalite veins; initial production from this yielded small, high-value crystals averaging 0.15-0.75 carats, revolutionizing the gem market. 's tourmaline exports, primarily from pegmatites, form a substantial portion of global gem trade, with annual production exceeding 8 tons from major operations like Cruzeiro alone, supporting an industry valued in the millions.

Africa and Asia

Africa hosts several prominent tourmaline deposits, with emerging as a leading global source for gem-quality varieties, particularly . The island's fields, such as those near Anjanabonoina, yield bi-color and parti-colored crystals exhibiting striking in pink, green, and multicolored patterns, often fashioned into step-cut gems. National tourmaline production in reached an estimated 120 kg annually in 2018 and 2019, contributing significantly to the country's gem exports, though exact global shares vary by year and type. In , the produces distinctive blue indicolite tourmaline, prized for its electric blue to mint green hues and high clarity, sourced from s in areas like Neu Schwaben and Usakos. Tanzania's Umba Valley is renowned for green dravite tourmaline displaying the Usambara effect, where crystals shift from green to red under varying light paths due to and impurities. Artisanal mining dominates tourmaline extraction across these African localities, presenting challenges including child labor, health risks from dust inhalation and accidents, and from unregulated pits. In eastern of Congo, similar artisanal operations for tourmaline have boomed since 2012 amid rising prices, drawing thousands of miners but exacerbating and conflict over sites. These issues underscore the need for improved to mitigate social and ecological impacts in the region. In , Afghanistan's Dara-e-Pech (Pech ) pegmatite field supplies pink to polychrome , including light pink with glassy terminations and vivid zoning. Pakistan's Swat hosts gem pockets in schists associated with emerald deposits, yielding Cr-bearing green tourmaline alongside dravite varieties. Myanmar's area is famed for tourmaline, often in unique "mushroom" or forms with raspberry pink to burgundy red colors on matrix. Post-2010 conflicts in these Asian regions have disrupted tourmaline supply chains; in , ongoing instability has limited access to Pech mines and increased smuggling risks for gem materials. Pakistan's Swat Valley faced militant insurgencies until around 2014, temporarily halting operations and reducing output, while Myanmar's ethnic conflicts in ruby-sapphire areas indirectly affected nearby mining logistics. These hydrothermal settings continue to yield diverse tourmaline, though security challenges persist.

Europe and Other Regions

Tourmaline occurrences in Europe are primarily associated with historical and type localities in igneous and metamorphic settings, contributing to scientific understanding of the mineral group rather than significant commercial output. The island of , , serves as the type locality for , a lithium-rich variety, with notable specimens from the Rosina vein in San Piero in Campo, where yellow-orange crystals occur in pegmatitic druses within aplitic dykes. These crystals, often found alongside and , highlight the mineral's role in boron-enriched late-stage magmatic processes in the Tuscan magmatic province. In , dravite, the magnesium-rich end-member, is documented in metamorphic environments such as metasomatized limestones and rocks in the region, including sites along the River valley, where it forms prismatic crystals with , , and . Sweden's Utö Island features schorl, the iron-rich variety, embedded in granitic pegmatites and associated with boron during the , as seen in the Nyköpingsgranite intrusions, where black tourmaline crystals appear in - matrices. In and , tourmaline deposits are linked to lithium-bearing pegmatites and metamorphic terrains, though extraction remains limited. Western Australia's hosts lithium-rich tourmaline, particularly , in LCT-type pegmatites such as those near Southern Cross, where it occurs as accessory minerals in spodumene- and petalite-bearing zones formed through fractional crystallization of granitic melts. These occurrences underscore the region's role in global resources, with tourmaline serving as an indicator of enrichment in Archean-aged intrusions. On New Zealand's West Coast, metamorphic tourmaline, including dravite-schorl intermediates, appears in ose rocks of the Haast Schist belt around , derived from regional metamorphism of sequences during the , often as disseminated needles or veins with and in low- to medium-grade . Occurrences in oceanic and Antarctic regions are rare and scientifically significant, often involving deep-seated or altered crustal materials with minimal economic impact. Tourmaline has been identified in ophiolitic sequences representing ancient , such as in and hosted in chromitites, where it forms as products during subduction-related processes. In , tourmaline-mineralized brittle faults in the Ford Ranges of reveal fluid-rock interactions in extended continental margins, with schorl and dravite varieties filling mirrored fault surfaces in granitic and metamorphic host rocks. These finds, including potential micro-inclusions in diamond-bearing assemblages from mantle-derived oceanic settings, contribute minimally to global tourmaline production, which is dominated by major gem districts elsewhere.

Uses and Applications

Gemology and Jewelry

Tourmaline is evaluated in based on the standard 4Cs—color, clarity, cut, and carat weight—though its strong and variable (7–7.5 on the ) require specialized considerations for jewelry use. Clarity is a key factor, with eye-clean stones (free of visible inclusions to the naked eye) highly preferred, particularly for green varieties; pink and red tourmalines can tolerate some eye-visible inclusions if the color saturation remains vivid, while inclusions like liquid-filled tubes may enhance value by producing a desirable cat's-eye effect in certain specimens. In the highly prized Paraíba tourmaline, however, color is the primary value driver, with clarity considered secondary. Inclusions are common in this variety and are generally tolerated, with eye-clean stones commanding a premium, though the price impact of inclusions is relatively minor compared to most other gemstones. Eye-visible inclusions typically cause only slight value reductions, while heavy inclusions can reduce value more noticeably if they affect transparency. Cutters often fashion tourmaline into slender rectangular or emerald-cut shapes to align with the elongated and minimize material waste, orienting the table facet parallel to the c-axis for lighter tones or perpendicular for deeper colors to optimize appearance; faceting maximizes brilliance and showcases (displaying multiple colors from different angles), whereas cabochons are used for stones exhibiting . Carat weight significantly impacts pricing, with fine specimens over 5 carats commanding premiums; for example, vivid tourmaline, prized for its neon blue-green hues due to content, prices can range from several thousand dollars per carat for lower-quality or non-Brazilian material to over $100,000 per carat for exceptional Brazilian specimens, as of 2025; however, synthetic versions fail to match the intense electric neon blue glow of natural specimens due to challenges in replicating the precise copper and manganese concentrations responsible for this effect. In historical jewelry, tourmaline gained popularity during the Victorian era (1837–1901), particularly in the late 1800s, when American-sourced pink and green varieties from California and Maine were promoted by Tiffany & Co. gemologist George F. Kunz, leading to its use in brooches, rings, and earrings that highlighted multicolored or zoned stones. These pieces often featured foil-backed settings to enhance color depth, reflecting the era's fascination with bold, natural gem contrasts. In modern jewelry design, tourmaline remains versatile, with artisans slicing bi-color or watermelon varieties (green exterior with pink core) into thin pendants or freeform shapes to preserve zoning patterns, as seen in contemporary collections from jewelers like Shaw Contemporary Jewelry. Tourmaline requires careful handling due to its sensitivity to heat and mechanical stress; exposure to high temperatures can alter color, cause fracturing from thermal shock, or destabilize liquid inclusions, while over-polishing or ultrasonic cleaning may scratch its surface or exacerbate brittleness. The (GIA) recommends cleaning with warm, soapy water and a soft , avoiding steam or ultrasonic methods, and provides identification reports for tourmaline but does not issue formal grading reports like those for . Black tourmaline, also known as schorl, is sometimes promoted in alternative medicine and crystal healing practices for purported therapeutic properties, such as protection from negative energy, electromagnetic fields (EMFs), or emotional grounding, as well as claims that it generates meaningful microcurrents—via its piezoelectric and pyroelectric properties—to provide benefits to the human body, including improved sleep when used in sleep pillows. While tourmaline exhibits piezoelectric properties (generating small electrical charges under mechanical pressure) and pyroelectric properties (generating charges under temperature changes), these effects are limited in magnitude, vary by sample, require external force or heat to activate, and produce only slight charges insufficient to provide therapeutic microcurrent stimulation comparable to controlled medical devices. There is no reliable scientific evidence supporting these health claims, which originate from metaphysical or alternative sources rather than rigorous studies; research, including a 2001 double-blind study by Christopher French, indicates that any perceived benefits are likely attributable to the placebo effect arising from personal beliefs and expectations.

Industrial and Scientific Uses

In materials engineering, finely ground tourmaline is incorporated as a filler in ceramics and plastics, enhancing thermal stability, mechanical strength, and chemical resistance owing to its inherent structural robustness and low reactivity. The piezoelectric properties of tourmaline, which generate an electric charge under mechanical stress, have been utilized in scientific instruments such as pressure transducers and sensors for high-precision measurements in geophysical and engineering applications. Additionally, tourmaline's thermoluminescence response to radiation enables its use in radiation dosimeters, where it records cumulative exposure doses through glow curve analysis, particularly valuable for high-dose monitoring in environmental and nuclear contexts. Emerging applications include tourmaline's potential in water purification, where its far-infrared emission and ion-exchange capabilities are claimed to reduce heavy metal concentrations and restructure water clusters for improved filtration efficacy, though scientific validation remains limited and debated due to inconsistent performance across studies.

References

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