In ore deposit geology, supergene processes or enrichment are those that occur relatively near the surface as opposed to deep hypogene processes. Supergene processes include the predominance of meteoric water circulation (i.e. water derived from precipitation) with concomitant oxidation and chemical weathering. The descending meteoric waters oxidize the primary (hypogene) sulfide ore minerals and redistribute the metallic ore elements. Supergene enrichment occurs at the base of the oxidized portion of an ore deposit. Metals that have been leached from the oxidized ore are carried downward by percolating groundwater, and react with hypogene sulfides at the supergene-hypogene boundary. The reaction produces secondary sulfides with metal contents higher than those of the primary ore. This is particularly noted in copper ore deposits where the copper sulfide minerals chalcocite (Cu2S), covellite (CuS), digenite (Cu18S10), and djurleite (Cu31S16) are deposited by the descending surface waters.[1]
All such processes take place at essentially atmospheric conditions, around room temperature (25 °C) and standard atmospheric pressure (1 atm).[2]
Zones
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Distinct zones of supergene processes can be identified at various depths. From the surface down they are the gossan cap, leached zone, oxidized zone, water table, enriched zone (supergene enriched zone) and primary zone (hypogene zone).[3]
Gossan cap
editPyrite (FeS2) has oxidised to form goethite (FeO(OH)) and limonite (FeO(OH)·nH2O),[2] which form a porous covering over the oxidized zone known as a gossan cap or iron hat.[4] Prospectors use gossan as an indication of ore reserves.
Leached zone
editGroundwater contains dissolved oxygen and carbon dioxide. As it travels downwards it oxidizes primary sulfide minerals, concomitant with forming sulfuric acid and solutions of oxidized metals.[5] For example, groundwater commonly interacts with pyrite (FeS2) to form an oxidized iron (FeO(OH)) and sulfuric acid (H2SO4), portrayed in the idealized chemical reaction below (intermediate steps omitted):
- 4 FeS2 + 12 H2O + 15 O2 → 4 FeO(OH) + 8 H2SO4
An intermediate in this process is ferric sulfate (Fe2(SO4)3), which oxidizes pyrite and other sulfide minerals.[6]
Oxidized zone
editAbove the water table the environment is oxidizing, and below it is reducing.[7] Solutions traveling downward from the leached zone react with other primary minerals in the oxidised zone to form secondary minerals[5] such as sulfates and carbonates, and limonite, which is a characteristic product in all oxidised zones.[3]
In the formation of secondary carbonates, primary sulfide minerals generally are first converted to sulfates, which in turn react with primary carbonates such as calcite (CaCO3), dolomite (CaMg(CO3)2) or aragonite (also CaCO3, polymorphic with calcite) to produce secondary carbonates.[4] Soluble salts continue on down, but insoluble salts are left behind in the oxidised zone where they form. Examples of insoluble salts that are commonly found in the oxidized zone include lead precipitates like anglesite (PbSO4) and pyromorphite (Pb5(PO4)3Cl); copper precipitates like malachite (Cu2(CO3(OH)2), azurite (Cu3(CO3)2(OH)2), and cuprite (Cu2O); and smithsonite (ZnCO3).[3][7]
Water table
editAt the water table the environment changes from an oxidizing environment to a reducing one.[7]
Enriched zone
editCopper ions that move down into this reducing environment form a zone of supergene sulfide enrichment.[3] Covellite (CuS), chalcocite (Cu2S) and native copper (Cu) are stable in these conditions[7] and they are characteristic of the enriched zone.[3]
The net effect of these supergene processes is to move metal ions from the leached zone to the enriched zone, increasing the concentration there to levels higher than in the unmodified primary zone below, possibly producing a deposit worth mining.
Primary zone
editThe primary zone contains unaltered primary minerals.[5]
Mineral alterations
editChalcopyrite CuFeS2 (primary) readily alters to the secondary minerals bornite Cu5FeS4, covellite CuS and brochantite Cu4SO4(OH)6.[5]
Galena PbS (primary) alters to secondary anglesite PbSO4 and cerussite PbCO3.[2][5]
Sphalerite ZnS (primary) alters to secondary hemimorphite Zn4Si2O7(OH)2.H2O, smithsonite ZnCO3 and manganese-bearing willemite Zn2SiO4.[2][5]
Pyrite FeS2 (primary) alters to secondary melanterite FeSO4.7H2O.[5]
If the original deposits contain arsenic and phosphorus bearing minerals, secondary arsenates and phosphates will be formed.[5]
Etymology
editThe word supergene is derived from the Latin root super meaning 'above' and the Greek root -gene (-γενής) meaning 'born' or 'produced'. The terms supergene and hypogene refer to the depth at which they occur.
See also
editReferences
edit- ^ Guilbert, John M. and Charles F. Park Jr (1986) The Geology of Ore Deposits, W. H. Freeman, ISBN 0-7167-1456-6
- ^ a b c d Manual of Mineralogy (1993) Klein and Hurlbut. Wiley
- ^ a b c d e Understanding Mineral Deposits (2000). Kula C Misra. Kluwer Academic Publishers
- ^ a b The Encyclopedia of Gemstones and Minerals (1991). Martin Holden. Publisher: Facts on File
- ^ a b c d e f g h Field Guide to North American Rocks and Minerals (1992) The Audubon Society. Alfred A Knopf
- ^ Harraz, Hassan Z. (2012), Topic 9: Supergene enrichment, Tanta University
- ^ a b c d John Rakovan (2003) Rocks & Minerals 78:419