Trachyandesite

Botswana Agate tumbled is an elegant type of Agate with white, black, grey, and occasionally blue bands. Found only in the Bobonong district of Botswana, this agate takes a very fine polish. It is commonly cut into cabochons and it's often used with jewelry, particularly rings.

Leucite is a rock-forming mineral of the feldspathoid group, silica-undersaturated and composed of potassium and aluminium tectosilicate KAlSi2O6. Crystals have the form of cubic icositetrahedra but, as first observed by Sir David Brewster in 1821, they are not optically isotropic, and are therefore pseudo-cubic. Goniometric measurements made by Gerhard vom Rath in 1873 led him to refer the crystals to the tetragonal system. Optical investigations have since proved the crystals to be still more complex in character, and to consist of several orthorhombic or monoclinic individuals, which are optically biaxial and repeatedly twinned, giving rise to twin-lamellae and to striations on the faces. When the crystals are raised to a temperature of about 500 °C they become optically isotropic and the twin-lamellae and striations disappear, although they reappear when the crystals are cooled again. This pseudo-cubic character of leucite is very similar to that of the mineral boracite. The crystals are white or ash-grey in colour, hence the name suggested by A. G. Werner in 1701, from λευκος, '(matt) white'. They are transparent and glassy when fresh, albeit with a noticeably subdued 'subvitreous' lustre due to the low refractive index, but readily alter to become waxy/greasy and then dull and opaque; they are brittle and break with a conchoidal fracture. The Mohs hardness is 5.5, and the specific gravity 2.47. Inclusions of other minerals, arranged in concentric zones, are frequently present in the crystals. On account of the color and form of the crystals the mineral was early known as 'white garnet'. French authors in older literature may employ René Just Haüy's name amphigène, but 'leucite' is the only name for this mineral species that is recognised as official by the International Mineralogical Association.

Carnallite (also carnalite) is an evaporite mineral, a hydrated potassium magnesium chloride with formula KMgCl3·6(H2O). It is variably colored yellow to white, reddish, and sometimes colorless or blue. It is usually massive to fibrous with rare pseudohexagonal orthorhombic crystals. The mineral is deliquescent (absorbs moisture from the surrounding air) and specimens must be stored in an airtight container. Carnallite occurs with a sequence of potassium and magnesium evaporite minerals: sylvite, kainite, picromerite, polyhalite, and kieserite. Carnallite is an uncommon double chloride mineral that only forms under specific environmental conditions in an evaporating sea or sedimentary basin. It is mined for both potassium and magnesium and occurs in the evaporite deposits of Carlsbad, New Mexico; the Paradox Basin in Colorado and Utah; Stassfurt, Germany; the Perm Basin, Russia; and the Williston Basin in Saskatchewan, Canada. These deposits date from the Devonian through the Permian Periods. In contrast, both Israel and Jordan produce potash from the Dead Sea by using evaporation pans to further concentrate the brine until carnallite precipitates, dredging the carnallite from the pans, and processing to remove the magnesium chloride from the potassium chloride. Carnallite was first described in 1856 from its type location of Stassfurt Deposit, Saxony-Anhalt, Germany. It was named for the Prussian mining engineer Rudolf von Carnall (1804–1874).

Seraphinite tumbled has a deep green or grey color with silvery, light veins that make it appear as though it contains feathers. This deems it very attractive and aesthetically pleasing. Seraphinite tumbled is only found in Russia. It has gem quality and is a popular collector’s stone. It can be made into beads for bracelets and necklaces.

Chabazite (UK: /ˈkæbəzaɪt/) is a tectosilicate mineral of the zeolite group, closely related to gmelinite, with the chemical formula (Ca,K2,Na2,Mg)Al2Si4O12•6H2O. Recognized varieties include Chabazite-Ca, Chabazite-K, Chabazite-Na, and Chabazite-Sr, depending on the prominence of the indicated cation. Chabazite crystallizes in the triclinic crystal system with typically rhombohedral shaped crystals that are pseudo-cubic. The crystals are typically twinned, and both contact twinning and penetration twinning may be observed. They may be colorless, white, orange, brown, pink, green, or yellow. The hardness ranges from 3 to 5 and the specific gravity from 2.0 to 2.2. The luster is vitreous. It was named chabasie in 1792 by Bosc d'Antic and later changed to the current spelling. Chabazite occurs most commonly in voids and amygdules in basaltic rocks. Chabazite is found in India, Iceland, the Faroe Islands, the Giants Causeway in Northern Ireland, Bohemia, Italy, Germany, along the Bay of Fundy in Nova Scotia, Oregon, Arizona, and New Jersey.