General Flashcards

1
Q

Syngenetic Deposits

A

This term describes terms that were formed at the same time as the host rocks. They are most commonly sedimentary.

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2
Q

Epigenetic deposits

A

These are ores that form after the host rocks. This is common within metasomatic and vein-related deposits.

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3
Q

Hypogene and supergene deposits

A

Hypogene: ores that form because of an ascedning solution Ex: Mississippi-style Pb-Zn
supergene: ores that form because of a descending solution. Ex: meteoric waters in Bisbee

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4
Q

Endogenetic and Exogenetic

A

Endogenetic refers to ores that form because of internal Earth processes. These are metamorphic or igneous processes.
Exogenetic refers to ores that form because of Earth surface processes, likely exogenetic. These are driven by external energy sources (primarily the sun).

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5
Q

Associations of ultramafic, intrusive mafics, intrusive intermediates, and felsic intrusives with ores

A

UMF: Ni, Cr, Pr
Intrusive mafics (gabbro + niorite): Cu, Co, Ni, Fem Ti, V
Intrusive intermediates (andesites): Cu, Au
Granites: Be, Li, Sn, W

These differentiation of elements is driven by fractional crystalization within the Goldschmidt series.

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6
Q

Economic Geology

A

The branch of applied geology concerned with the discovery, understanding and extraction of non-fuel resources from the Earth

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7
Q

Mineral deposits

A

Earth materials that contain anomolous amounts of minerals or elements

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8
Q

Ore deposits

A

Ore deposits or economic deposits are reflective of human need for the mineral and represent a sub-sector of mineral deposits that we mine. They are made of one or more ore bodies.

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9
Q

World-class deposits

A

These are deposits in the uppermost 10% of the grade, tonnage plot (meaning the upper 10% of total reserves) they are important because as size increases economies of scale magnify and they also provide usually >70% of the supply of the mineral resource

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10
Q

Periodic table trend: atomic radius

A

Atomic radius increases in the lower left of the table, francium is the largest

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11
Q

Enrichment factor meaning

A

This is the ratio of the concentration of the element within ore deposits divided by the crustal abundance. Generally as crustal abundance decreases the enrichment factor increases.

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12
Q

Trace metal abundance curve vs. major

A

The major elements follow a normal curve and ore deposits are on the uppermost tail. Trace elements are bimodal with the higher grade hump’s right tail being those that are ore deposits.

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13
Q

$/ton of ore vs. tonnes production

A

As the $/tonne increases the tonnes produced decreases. Ex: Rhenium and diamonds have very few tonnes produced but have a major $/tonne value. Iron is produced in mass with a low $/tonne

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14
Q

Ore minerals

A

These are minerals that are either opaque in thin section (according to normal geologists) or those that contain economically important minerals

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15
Q

Mineral assemblages

A

These represent a form of chemical equilibria where the minerals co-evolve. They are usually intergrown, replace one another, and obey the phase rule.

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16
Q

How can we plot most rocks in terms of their composition?

A

There can be a plot of the summation of (Ca, Mg, Fe2+) vs. summation of K and Na.

17
Q

Equilibrium

A

This describes a state without a spontaneous tendency to change. It can be stable, metastable, or unstable but always reflects some type of minima of PE.

18
Q

Chemical Equilibrium

A

This is where delta G is at a minimum

19
Q

Phase Rule

A

Prescribes the maximum number of phases (fluid, solid, or gas) at equilibrium through f=c+p-2 where c= # of components, p = #of phases, f= degrees of freedom

20
Q

Mineral Associations

A

These are minerals that often co-occur but are not always at equilibrium with one another upon formation.

21
Q

Goldschmidt Classification

A

Lithophile - elements that bond with oxygen - silicates and oxides
chalcophile - elements that bond with sulfur - MS
siderophile - Native elements, alloys, or with Fe
atmophile - gaseous elements

22
Q

Elemental partitioning

A

A term describing how minerals separate during phase changes. Generally, smaller radius low chare ions that substitute into Fe, Mg, Ca sites will be sequestered in the mantle and larger ions will make it to the crust.

23
Q

How do sizes of ions change with charge and with position in the periodic table and why is this important in crystals?

A

Cations are much smaller than anions so the anion-anion repulsion of atoms around a central cation is the major determinant of crystal structure. This means that the cation size (which dictates the distance between anions) is important.

24
Q

List the major mineral groups and what distinguishes each group

A

Oxides- MOx atmophile
Sulfides - MSx S <-> O at shallow depths or under oxidizing conditions
Sulphates - Mx (SO4)x
Carbonates
Phosphates
all three are potentially water soluble and form in acidic conditions
Salts
Silicates - Mx Sx Ox the most common mineral group in the crust
Native minerals - always CCC

25
Q

What general principle governs substitutions in minerals?

A

Pauling’s rules;
1. the coordination number of the cation/anion is determined by the ration of their raii
2. bond lengths are determined by ionic charge and coordination number
3. shared polyhedra faces are less stable
4. higher valency cations are less likely to share faces
5. There are a few select types (size, charge) within a crystal.

26
Q

What are the three major geotherms?

A

Subduction zones - low T - ultrahigh P, goes through blueschist and eclogite facies ~10 C/km
Continental crust - Average ~ 22 C / km goes through the greenschist and amphibolite facies to eventually become granulite
Magmatic arc - high ~50 C/km These border greenschists and hornfels

27
Q

What is the brittle-ductile transition?

A

It is the point below the surface where rocks start behaving like viscous fluids mechanically, basically it is where they no longer follow Mohr-Coloumb failure criterion and instead deform indefinitely following fluid mechanics.

28
Q

Nernst Partition Coefficient

A

This is the ratio (Kia/b = ci a / ci b ) where c is the concentration of element i in phase a or b.
It is dependent on T, P, and composition but generally assumed constant for a given stage of magmatic evolution.

29
Q

Bulk solid to liquid partition coefficient

A

D = Σ f i K ix where fi is the fraction of the element x in the system (not only in one phase.

30
Q

Element compatibility

A

This is the degree to which an element will substitute into the crystal lattice of a phase in a system. It is defined by K where if K>1 it is incompatible and there is more element in the melt than in the solids.

31
Q

Bowens Reaction Series

A

This is the tendency for mafic rocks and plagioclase (high Ca, Mg, and Fe 2+ ) crystalize at high temperatures deep underground and the silica rich rocks and K-spar crystalize at low temperatures near the surface