Magmatic hydrothermal Flashcards

1
Q

Magmatic hydrothermal systems: key feature, main commodities, deposit types

A

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

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2
Q

What is a typical P-T range for M-H deposits? What are some of the variables that determine their form?

A

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

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3
Q

What is the importance of physical characteristics of the exsolved fluids?

A

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.

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4
Q

What is the role of water immiscibility in M-H systems in relation to the need for an oxidized magma?

A

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.

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5
Q

Components of a mineralizing hydrothermal system

A
  • 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
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6
Q

Clarke factor of concentration

A

This is the V(deposit)/V(leached rock or magma)

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7
Q

How does solutbility change as a f(valence, radii)?

A

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.

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8
Q

Ligands

A

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.

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9
Q

What is the composition of magmatic-hydrothermal-solutions?

A

These are H-O-Si-O…, H2O, CO2, HCl, CH4, H2S, SO2 rich fluids (volatile!)

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10
Q

First and second boiling

A

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.

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11
Q

Common alteration types and related T and pH

A
  1. Advanced argillic - low pH (1-2) with T 700-150 C - andalusite at high T, pyrophyllite, and kaolinite
  2. Sericitic - sericite + chlorite at mid T and mid pH creates characteristic sericite haloes overprinting potassic
  3. Intermediate argillic - alumino-silicates - pH ~ 4 T ~ 200-400
  4. Propylitic - epidote, sericite ~400 C from the dispersed volatile rich fluids without acids
  5. Potassic - high T (700) and K-spar, qtz, biotite - metasomatic
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12
Q

Alteration inidicators

A

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)

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13
Q

How to tell if fluids are magmatic vs. hydrothermal for alteration?

A

Magmatic fluids emplace Qz + Bi + K-spar in potassic alteration, Meteoric fluids replace quartz with albite

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14
Q

Skarn: def, commodities, size, geometry, location

A

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.

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15
Q

Skarn minerals

A

Ca - wollastonite (CaSiO3), Ca-garnet (Ca3Fe2(SiO4)3), andradite, pyroxene
Mg - pyroxene (XYSi2O6), serpentine (Mg3Si2O5(OH)4), pyrite (FeS2)

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16
Q

Primary processes involved with metal precipitation

A
  1. Cooling: As temperature decreases the solubility of metals in solution significantly decreases -> UST
  2. Wall rock reactions with acids on carbonates reduce the solution and lower the metal solubility
  3. Off-gassing and de-pressurizing
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17
Q

Metal solubility trend

A

Fe > Pb ~Ag~ Zn > Cu > Mo

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18
Q

Paragenisis

A

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.

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19
Q

Equation for approximate cooling time

A

1 ~ K/(t * a2)
Where: K = thermal diffusivity
t = years
a = 1/2 of the shortest distance from the igneous feature to the surface

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20
Q

Types of fluid inclusions

A

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

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21
Q

Porphyry Copper: general features, magma composition, locations, commodities, and geometry

A

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

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22
Q

What is the importance of oxidation state in porphyry Cu?

A

If H2 S is present (S is reduced) then Cu-S compounds will form and become part of the granite but if oxidized so SO2 is present then the Cu will remain in solution to be deposited.

23
Q

Veins

A

These are tabular bodies within spaces either via hydrofracturing or pre-existing voids
open veins describe veins that have foreign materials inside and closed veins are shut
It favors the precipitation of minerals that have solubilities dictated by changes in pressure and temperature (like sio2).
Lode deposits are composed of many vein sets.

24
Q

Cupolas

A

Dome-shaped areas that are clearly influenced by intruding magmatic stocks

25
Q

What is the relationship between magma composition and metal precipitates?

A

monzo-granitic magmas (LR of ternary) are Mo and Cu is more dioritic/mafic (in the center of the diagram)

26
Q

What are key characteristics of porphyry deposits?

A

These are defined by a very large volume (1Mt-10Gt) ore within evenly distributed vein systems at <1% Cu, 1 ppm Au, .1% Mo. The intrusions at the center are relatively small

27
Q

Porphyry: distribution and geometry

A

These are relatively young <75 myr which makes sense because they are on volcanic arcs that are easily eroded and are not incredibly deep. Geometrically they are considered the bases of strato-volcanos and are composed of many heterogeneous intrustions

28
Q

Geometry of ore in porphyry

A

There are multiple kinds of veins and these tend to form systematic sheets or stocks that indicate relative tension with respect to the intruding magma meaning that they tend to form tangential to the intrusion and normal to the intrusions

29
Q

Unidirectional solidification texture

A

These are most common within the plutons below the porphyry system and is marked by irregular lobe-like quartz druzy forming layers with quenched magmatic materials. It shows that the growth of the materials was unidirectional.

30
Q

What is the general sequence of events for porphyry formation?

A
  1. magmatic intrusion related to the rise and colling of the hydrated, felsic-int. magmas causing USTs and first boiling
  2. Build up + release of fluids related to the convection and collection of fluids in the cupola until reaching critical fraccing pressures
  3. Later intrusions and sources of heat continue to repeat the process causing increased ore concentration and the overprinting of prior minerlization events
31
Q

Greisens: def, commodities, size, notable locations

A

These are hydrothermal alteration of granitic rock specifically related to B and F rich minerals like fluorine, topaz, and/or tourmaline. These are relatively small (10-100Mt) deposits of Sn, W, Cu, Zn, Bi, and Mo like in Cornwall

32
Q

Greisen geometry and geology with respect to porphyry

A

These are driven by equigranular intrusions that are more fractionated luecogranites that form greisen veins that are sub-tangential to the intrusion - similar to pegamtites but not as complex

33
Q

Fluid composition and function for greisens

A

Fluids are typically 250-450 C and the ore minerals are complexed with Cl and either replace or alter the minerals to form the typical greisen minerals

34
Q

Carbonate replacement: def, geometry, examples, commodities

A

These are usually 2-4 km from the heat source and are the complete replacement of CO3 marl-like rocks with epidote, pyroxene, garnet, and sulfide ore minerals. They are in chimneys, karsts/caves, and mantos and form because of the buffering of acidic solutions with the lime at 300-600 C and grades 10-10X that of skarns for Sn, W, Mo Bi, U, Au, Ag, Cu, Zn. Notably the giant silver deposits of N. MX. Replacement deposits have calcite.

35
Q

Common zoning patterns with distance from a magmatic intrusion

A

Close (600C): W-Bi -> Sn -> Sn-Cu-Pb-Zn-As -> Pb-Ag-Zn-Cu far (250 C)

36
Q

High sulfidation epithermal: def, commodities, major processes, geometry, and examples

A

This is defined by Au, Ag, Cu within intensely altered rock (where S fugacity is high). It is relatively shallow (<1.5 km) and ~1-2 km from the magma source. They are commonly just below the lithocap of volcanic materials. They are found in fairly heterogenous ore bodies within vuggy silica surrounded by advanced argilic alterations (alunite-kaolinite) that grade into argilic on the edges.

37
Q

Carbonate replacement processes

A

Basically the fluids dissolve the carbonates and this raises the pH. Upon the dissolution of the carbonates, SiO2 + CaCO3+ H2S + M+ = H2CO3 + MS + CaFeSi2O6 and Zn2+ + H2S = ZnS + 2H

38
Q

High sulfidation processes

A

The fluids are ~250 C with pH ~1-2 with relatively low salinity (2-10% NaCl) and at this temperature the vapors can become liquids which means that H2S and H2SO4 go into solution rapidly lowering the pH, dissolving non-quartz and creating a low-P vugh for ore formation.

39
Q

Paragenetic Sequence

A

This describes characteristic zones of mineralization related to time synchronous events. For example, sericitiv alteration with type A/B copper veins within a Cu porphyry.

40
Q

What are aqueous complexes and which are most important?

A

These the the development of metals surrounded by water due to polarity. The most important three are H2S (Cu, Ag, Au, Hg, Ti, As, and Sb), Cl, and OH

41
Q

Hydrtothermal alteration

A

The process whereby hydrothermal fluids react with rocks to change composition via metasomatism

42
Q

What is vein fill and alteration envelopes?

A

Vein fill refers to the gangue and small quantities of ore that are within the previously open viens. Alteration envelopes are the areas around the vein that have undergone hydrothermal alteration.

43
Q

skarnoid

A

This is where similar rocks near one another exchange mass without significant metasomatism. For example, exchanging Si in interbedded clastic and carbonate beds that are exposed to regional meta.

44
Q

What does K/Na for fluids indicate?

A

This indicates the fluid source as magmatic fluids tend to have more K and terrestial fluids more Na

45
Q

How does iron interact within M-H systems?

A

Fe is everywhere so it is almost inevitably preceipitated within the deposits. The oxidation/reduction of the fluids dictates the minerals formed.

46
Q

What minerals would form in a limestone skarn vs. dolostone vs. siltstone?

A

In limestone garnet, wollastonite and calcite would form. In dolostone the 50:50 Mg:Ca ratio forms diopside, tremolite, and talc. Pyroxene within siltstones.

47
Q

How are H and O used to ID the source of fluids?

A

Rocks have alot more O than H, particularily 18O, which means that when water percolates through them that they deviate from SMOW and/or when magmatic waters and terrestial waters mix

48
Q

Alunite

A

This is a low T sheet silicate that forms when the activity of H2SO4 is high

49
Q

How do lodes and replacement deposits compare and contrast?

A

Lodes are different from replacement because they do not necessitate a reaction with the wall rocks like replacement does. They are commonly co-associated (like in MX) and reflective of low to mid T hydrothermal fluids.

50
Q

Mantos

A

These are CO3 replacement deposits that form flat lying (related to preferrential dissolution) high grade deposits of Cu, Zn, Ag, Au (~2-3%).

51
Q

What are some of the most common skarn minerals and their associated timings?

A

Garnets: early, high-T, -> andradite is high Ca
Pyroxenoids: early and around the garnet
Amphiboles, sheet silicates, and FeOs: are all later in the process and superimpose the garnets/pyroxene
Sulfides: mid-late in the process and distal
Quartz and CO3 minerals: distal to skarn and late

52
Q

Compare and contrast metasomatism (like skarns) and metamorphism (like hornfels)

A

Metasomatism has very few minerals involved but high variance across deposits. Metamorphic processes produce a set of very similar diverse minerals regardless of the localle.

53
Q

Chimneys

A

These are a type of metasomatic deposit which are “dyke like” in geometry, meaning that unlike their oftentimes associated mantos, they are perpindicular to the dominant bedding in a region.

54
Q

Felsic skarns

A

These are W and lithophile (F, Be, Zn, Mo, Sn, W) skarns that form because of the more fractionated source magma and associated fluids. They are typically reduced magmas that are on the order of 100,000 tonnes (slightly smaller than other skarns)