Cesanite
Cesanite is the end member of the apatite-wilkeite-ellestadite series that substitutes all of apatite's phosphate ions with sulfate ions and balances the difference in charge by replacing several calcium ions with sodium ions. Currently very few sites bearing cesanite have been found and are limited to a geothermal field in Cesano, Italy from which its name is derived, Măgurici Cave in Romania, and in the San Salvador Island caves in the Bahamas.
History
Cesanite was first discovered in 1981 while the Italian National Electricity Board was doing exploratory drilling to examine a reservoir of heated brine to determine its potential as a geothermal energy source. When it was first found it was thought to be an apatite until after more thorough examination.Structure
Cesanite was originally determined by Tazzoli to be isotypic to that of hydroxylapatite. This was determined by refining the original unit cell dimensions and comparing them to the atomic coordinates of Holly Springs hydroxylapatite. From this it was extrapolated that although different elements are substituted for cesanite, the structure and cell parameters are nearly the same with some differences in the bond lengths of the tetrahedra. This similarity was to confirm the space group P3/m previously assigned to cesanite, this changed in 2002 after a reexamination of cesanite by Piotrowski et al. was prompted by its similarities to a synthetically produced analog. After this study it was found that the crystal structure of cesanite to be isostructural to this synthetic analog with the chemical formula Ca2Na3. What can be inferred from this is that while hydroxylapatite remains similar in its chemical formula it is not longer to be considered a structural analog. The new correct space group is P. It can be inferred that the reason the mistake went unnoticed for so long is that cesanite retains pseudo-symmetry in the array of its tetrahedra that closely mimics P3/m.Cesanite's crystal structure is made up of tetrahedra of sulfide cations surrounded by oxygen anions distributed along with hydroxide ions around the Ca and Na ions occupying the M1 through four sites. The M1 and M2 cites create distorted pentagonal bipyramids while the M3 and M4 create tricapped trigonal prisms. The M3 and M4 polyhedra share faces when they are next to each other and form columns parallel to while isolated sulfate tetrahedra alternate along the c axis.