 
                             Aragonite           is a common carbonate mineral. It is unfortunately often thought of as           the poor cousin to calcite. But aragonite is an interesting and           attractive mineral in its own right. It forms interesting habits and           can have a soft pretty color. Its modes of formation and relationship           to calcite are both curious and intriguing.
          
           Aragonite is a polymorph of calcite, which means that it has the same           chemistry as calcite but it has a different structure, and more           importantly, different symmetry and crystal shapes. Aragonite's more           compact structure is composed of triangular carbonate ion groups (CO3),           with a carbon at the center of the triangle and the three oxygens at           each corner. Unlike in calcite, the carbonate ions do not lie in a           single plane pointing in the same direction. Instead they lie in two           planes that point in opposite directions; destroying the trigonal           symmetry that is characteristic of calcite's structure. To illustrate           this, imagine the symmetry of an equilateral triangle; a three fold           rotation with three mirror planes that cross in the center. Now join           two of these triangles together at their bases and you have a           diamond-shaped figure with the symmetry of a two fold rotation with           one mirror plane in the middle. This is what the effect of the two           carbonate planes with opposite orientations has on the symmetry of           this structure. Aragonite has an orthorhombic symmetry (2/m 2/m 2/m)           instead of calcite's "higher" trigonal (bar 3 2/m) symmetry.           A very rare mineral called vaterite is also a polymorph of aragonite           and calcite; making them all trimorphs. Vaterite has an hexagonal           symmetry (6/m 2/m 2/m).
          
           Carbonate minerals with this same structure as aragonite belong to           the Aragonite Group of minerals. The structure is responsible for the           similar properties of this group. Dissimilar properties are the           responsibility or result of the differing metal cations in the various           minerals of the group.
          
           Aragonite is technically unstable at normal surface temperatures and           pressures. It is stable at higher pressures, but not at higher           temperatures such that in order to keep aragonite stable with           increasing temperature, the pressure must also increase. If aragonite           is heated to 400 degrees C, it will spontaneously convert to calcite           if the pressure is not also increased. Since calcite is the more           stable mineral, why does aragonite even form? Well under certain           conditions of formation, the crystallization of calcite is somehow           discouraged and aragonite will form instead. The magnesium and salt           content of the crystallizing fluid, the turbidity of the fluid and the           time of crystallization are decidedly important factors, but there are           perhaps others. Such areas as sabkhas and oolitic shoals tend to allow           significant amounts of aragonite to form. Also metamorphism that           includes high pressures and low temperatures (relatively) can form           aragonite. After burial, given enough time, the aragonite will almost           certainly alter to calcite. Sedimentologists are very interested in           aragonite and calcite stability fields because the conversion of           aragonite to calcite after deposition has a distinct effect on the           character of the sedimentary rocks.
          
           Aragonite's most famous crystal habit is the twinned pseudo-hexagonal           prismatic crystals that it produces. Twinning is the result of an           error during the growth of the crystal. It occurs when the atomic           layer stacking, in a sequence such as ABCABCABCABCABCABC etc, makes a           mistake and a C layer instead of a B layer is place next to an A           layer. The result is an ABCABCABCACBACBACBA stacking sequence (can you           pick out the mistake?). Where the mistake occurs, a mirror plane is           produced that was not there before (the left side is the mirror image           of the right side). This has the effect of increasing the apparent           symmetry of the crystal. The error in aragonite's structure causes a           bend in the crystal of exactly 120 degrees. If three bends or twins           occur, then a 360 degree crystal, called a cyclic twin or trilling,           can form. In this case, aragonite can appear hexagonal (six sided).            These crystals can be thought of as a "triple siamese twin"           where one crystal takes up one third (or 120 degrees) of a hexagon.
          
           Individual cyclic twins from Aragon, Spain have been popular but are           being surpassed by the amazing clusters of aragonite twins that are           now available from Morocco in large numbers. Aragon, Spain is where           aragonite was first discovered and from where aragonite gets its name.           Cyclic twins often show notches that separate the twin individuals.           Aragonite also has another popular habit called flos ferri or "flowers           of iron". This is a branching, clumpy habit that can make           delicate tree, coral or worm-like formations that are most unique. A           steep pyramidal habit forms clusters of sharp spiked crystals           sometimes referred to as a "church steeple" habit. Aragonite           is a constituent of many sea creatures' shell structures; a curious           development since calcite is the more stable form of calcium           carbonate. Most bivalve animals and corals secrete aragonite for their           shells and pearls are composed of mostly aragonite. The pearlization           and iridescent colors in sea shells such as abalone are made possible           by several minute layers of aragonite. Other environments of formation           include hot springs deposits, cavities in volcanic rocks, caves and           mines.