Carbonate-fluorapatite
Chemical formula: Ca<sub>5</sub>(PO<sub>4</sub>,CO<sub>3</sub>)<sub>3</sub>F
Calcium phosphate from the apatite group, in which some phosphate groups are replaced by carbonate groups; it is the main component of phosphorite rocks.
Properties
- Mohs hardness
- 5
- Luster
- Vitreous to resinous
- Streak
- White
- Density
- 3.1-3.2
- Cleavage
- Indistinct on {0001}
- Fracture
- Conchoidal to uneven
- Transparency
- Transparent to opaque
- Crystal system
- Hexagonal
Diagnostic features
## Identification A key diagnostic feature is a hardness of exactly 5 on the Mohs scale. If the mineral forms crystals, their hexagonal shape (hexagonal prisms) is very characteristic. In the case of massive and granular aggregates, identification is more difficult; relatively high density and vitreous luster can be helpful. A weak reaction with hydrochloric acid (when powdered) may indicate the presence of carbonates. ## Distinguishing from Similar Minerals Carbonate-fluorapatite is sometimes confused with beryl (much harder, 7.5-8), tourmaline (harder, 7-7.5, often shows striations on prism faces), and calcite (much softer, 3, reacts violently with acids). It can be distinguished from other apatite varieties mainly by advanced analytical methods. ## Crystal Forms Crystals, when they occur, have a habit of hexagonal prisms, often terminated by pyramids or flat pinacoids. However, it much more often forms granular, massive, radial, reniform (botryoidal), and spherical (oolitic) aggregates, as well as cryptocrystalline masses in phosphorites.
Geological environment
## Genesis Carbonate-fluorapatite is a mineral primarily of sedimentary origin. It forms in marine environments as a result of chemical and biochemical processes, leading to the accumulation and formation of extensive phosphorite deposits. It can also form during diagenetic processes and as a result of weathering of phosphorus-rich rocks. It is the basic building block of fossilized bones and teeth. ## Mineral Associations In phosphorite rocks, it most often co-occurs with calcite, dolomite, quartz, glauconite, pyrite, and clay minerals. In bone fossils, it is the main component, often with admixtures of iron and manganese oxides. ## Localities As the main component of phosphorites, it occurs in vast quantities in many places around the world. The most economically important and known for interesting specimens (mainly fossils) localities include Morocco (Khouribga region), USA (Florida, North Carolina, Idaho), China, Russia, Tunisia, and Jordan.
Rarity
Common
For collectors
## Quality Criteria For collectors, well-formed, sharp, and transparent crystals are most desirable, which are rare for this variety. However, interesting aggregate forms, such as reniform forms, spherical concretions, or oolites, are very popular. Exceptionally valued are well-preserved fossils (e.g., shark teeth, dinosaur bone fragments) composed of carbonate-fluorapatite, where the original bone structure has been replaced by this mineral. ## Popular Localities The most famous collector specimens in the form of fossils come from phosphorite basins in Florida, USA (e.g., Peace River area, mines in Polk County) and from Morocco. Massive, botryoidal, or oolitic forms can be found in all major phosphorite mining regions.
Care and storage
## Cleaning Specimens should be cleaned gently, using a soft brush and distilled water. Ultrasonic cleaners should be avoided, as they can damage specimens with internal fractures. ## What to Avoid The mineral is relatively soft (hardness 5), so it is easily scratched by harder minerals, such as quartz or beryl. It is sensitive to strong acids, which cause it to etch. Some colored varieties may fade with prolonged exposure to sunlight. ## Storage It is recommended to store specimens in separate, padded boxes or display cases to avoid contact with harder minerals. They should be protected from dust and sudden changes in temperature.