The mineral was originally named wilkeite by Eakle and Rogers in 1914, in honor of R. M. Wilke, a mineral collector and dealer. In 1922, a sample of “wilkeite” was analysed and found to be sufficiently different from the materialreported by Eakle and Rogers to consider it a new species. The name “ellestadite” was proposed, in honor of Reuben B Ellestad, an American analytic chemist from the Laboratory for Rock Analysis, University of Minnesota, US. In 1982 Rouse and Dunn showed that the Si:S ratio was close to 1:1, giving the formula Ca1033X2, where X represents fluorine, hydroxyl or chlorine, and they named minerals in this group the ellestadite group. The end members of the group were named hydroxylellestadite, fluorellestadite and chlorellestadite ; ideal end-member chlorellestadite is assumed not to exist in nature, although it has been synthesized. Wilkeite was discredited as a unique species, as it is not an end member of any solid solution series, but an intermediate member. The name fluorellestadite was changed to ellestadite- in 2008 and changed back to fluorellestadite in 2010.
Structure
The ellestadites are nesosilicates, which are minerals with isolated SiO4 tetrahedra. They are members of the apatite group, but whereas phosphorus is one of the chief constituents of apatite, in ellestadite it is almost completely replaced by sulfur and silicon, without appreciably altering the structure. The crystal class is hexagonal 6/m, space group P63/m. The tetrahedral groups are arranged to create the 63screw axis, and the fluorine atoms are located in channels parallel to this direction. Some sources give unit cell parameters for one formula unit per unit cell, but some scientists consider the formula to be half the value accepted by the International Mineralogical Association, i.e. Ca5)3F, with two formula units per unit cell. Cell parameters for natural, as opposed to synthetic, material are a = 9.41 to 9.53 Å, and c = 6.90 to 6.94 Å. Rouse and Dunn postulated a hypothetical pure end-member with a = 9.543 Å and c = 6.917 Å. Synthetic material has a = 9.53 to 9.561 Å, and c = 6.91 to 6.920 Å.
Appearance
Fluorellestadite occurs as acicular or hexagonal prismatic, poorly terminated crystals, and as fine-grained aggregates. Crystals are transparent and aggregates are translucent. Material from Crestmore, California, is light rose-red or yellow in color, and typically occurs in a matrix of blue calcite. Material from Russia is pale bluish-green or colorless. The streak is white with a weak bluish tint, and the luster is sub-resinous on broken surfaces, but very brilliant on prism faces.
Physical properties
Fluorellestadite shows imperfect cleavage perpendicular to the long crystal axis. The mineral is very brittle, and breaks with a conchoidal fracture. Its hardness is, between that of fluorite and apatite, and its specific gravity is 3.03 to 3.07, similar to that of fluorite. It is easily soluble in dilute hydrochloric and nitric acids and is not radioactive. When intensely heated, ellestadite becomes colorless and then assumes a pale bluish green color on cooling. The mineral is uniaxial, with refractive indices nω = 1.638 to 1.655 and nε = 1.632 to 1.650. It is sometimes fluorescent, white to blue-white or yellow-white in short-wave ultraviolet light, and medium white-yellow-brown or weak white in long-wave light.
