Magmatic hydrothermal Flashcards
Magmatic hydrothermal systems: key feature, main commodities, deposit types
These are systems that have their fluids mainly derived from a magma. They create porphyries, skarns, and replacement deposits which are essential for Cu, Mo, and Sn with Au, Ag, Zn, and Pb being by-products
What is a typical P-T range for M-H deposits? What are some of the variables that determine their form?
They are usually at ~900 C and 20 km where post cooling they are at 10 km and 700 C where they hit the wet granite solidus
What is the importance of physical characteristics of the exsolved fluids?
Water is usually within a supercritical state (with alot of dissolved solids) and this means that a small change in pressure causes a major change in density. This causes convection.
What is the role of water immiscibility in M-H systems in relation to the need for an oxidized magma?
If there is the formation of S2 through having a reduced melt (like LMI’s) then the copper in the melt will be partitioned into the solid. If the melt is oxidized then SO2 or SO4 will dominate and the metals will stay in solution to be precipitated as ore.
Components of a mineralizing hydrothermal system
- fluid source: f(magma) or meteoric waters
- source of dissolved ores
- fluid flow pathways
- energy source driving mass transport
- host rock
- chemical driver of ore precipitation
It necessitates a physical gradient for fluids to congregate and precipatate ore minerals
Clarke factor of concentration
This is the V(deposit)/V(leached rock or magma)
How does solutbility change as a f(valence, radii)?
high field strength elements and compounds are highly soluble as ions (think alkalai and alkalai E). Transition metals (plotting in the middle) are weakly soluble. The semi-metals are considered solutble. So in comparison to other elements metals are not as soluble. Generally as charge increases and radii decreases solubility increases.
Ligands
These are anions and anionic compounds tat increase the solubility of metals by creating a barrier around them in water. They are similar to acid strength and are selective in the metals that they complex. Chlorine (salty brines), H2S, and SO4 are key.
What is the composition of magmatic-hydrothermal-solutions?
These are H-O-Si-O…, H2O, CO2, HCl, CH4, H2S, SO2 rich fluids (volatile!)
First and second boiling
First boiling refers to the decompression exsolution of fluids when magmas are rising it takes fluids from an entrained state to a vapor or supercritical state. Second boiling is during crystalization where fluids are exsolved chemically. This is when concentration is most significant.
Common alteration types and related T and pH
- Advanced argillic - low pH (1-2) with T 700-150 C - andalusite at high T, pyrophyllite, and kaolinite
- Sericitic - sericite + chlorite at mid T and mid pH creates characteristic sericite haloes overprinting potassic
- Intermediate argillic - alumino-silicates - pH ~ 4 T ~ 200-400
- Propylitic - epidote, sericite ~400 C from the dispersed volatile rich fluids without acids
- Potassic - high T (700) and K-spar, qtz, biotite - metasomatic
Alteration inidicators
Replaced minerals are key so when there is a fine textured mineral within the shape of a common crystal (for example mica within an old hornblende crystal)
How to tell if fluids are magmatic vs. hydrothermal for alteration?
Magmatic fluids emplace Qz + Bi + K-spar in potassic alteration, Meteoric fluids replace quartz with albite
Skarn: def, commodities, size, geometry, location
A Ca +- Mg silicate-rich metamorphic rock replacing carbonates or, if endoskarns, replacing igneous rocks. They are small (1-10 Mt) but high grade (~2% Cu) with (Cu, Au), (W-Sn), Sn, (Zn-Pb) and form chimneys (cross strata) and mantos (blankets) with increased distance from the heat source they tend to form replacement deposits. These have wollastininite and mass is added to them.
Skarn minerals
Ca - wollastonite (CaSiO3), Ca-garnet (Ca3Fe2(SiO4)3), andradite, pyroxene
Mg - pyroxene (XYSi2O6), serpentine (Mg3Si2O5(OH)4), pyrite (FeS2)
Primary processes involved with metal precipitation
- Cooling: As temperature decreases the solubility of metals in solution significantly decreases -> UST
- Wall rock reactions with acids on carbonates reduce the solution and lower the metal solubility
- Off-gassing and de-pressurizing
Metal solubility trend
Fe > Pb ~Ag~ Zn > Cu > Mo
Paragenisis
This is a term used to describe the time-space relationships of events which for porphyries are usually complex with superposition and zoning. Specifically it is for associations and co-occurances of minerals.
Equation for approximate cooling time
1 ~ K/(t * a2)
Where: K = thermal diffusivity
t = years
a = 1/2 of the shortest distance from the igneous feature to the surface
Types of fluid inclusions
Primary are inclusions that occur during the crystal growth and will not cut accross different growth phases
Seconday are healed cracks and are fragmented lines cross-cutting the crystal growths
“Psuedo-secondary” are healed fractures that only cut through part of the growths
Porphyry Copper: general features, magma composition, locations, commodities, and geometry
Porphyry Cu (+- Mo, Au) are very large deposits (Btonnes) that form cupolas above felsic oxidized magmatic intrusions. They are generally hat-shaped with zoning based upon the solubilities of entrained metals. Notable locations include El Salvador (Chile), Bingham, and Yerington