New insights into the origin of the Evate apatite-iron oxide-carbonate deposit, Northeastern Mozambique, constrained by mineralogy, textures, thermochronometry, and fluid inclusions
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F17%3A00096233" target="_blank" >RIV/00216224:14310/17:00096233 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1016/j.oregeorev.2016.09.017" target="_blank" >http://dx.doi.org/10.1016/j.oregeorev.2016.09.017</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.oregeorev.2016.09.017" target="_blank" >10.1016/j.oregeorev.2016.09.017</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
New insights into the origin of the Evate apatite-iron oxide-carbonate deposit, Northeastern Mozambique, constrained by mineralogy, textures, thermochronometry, and fluid inclusions
Popis výsledku v původním jazyce
The Evate deposit represents the largest resource of apatite in south-east Africa (155 Mt. ore grading 9.3 wt.% P2O5) accumulated in up to 100 m thick magnetite-carbonate-apatite horizons conformable to the granulitic gneiss of the Monapo Klippe. Baddeleyite and zircon from early iron-oxide (magnetite, geikielite, spinel), apatite- and forsterite-bearing rocks have been dated to 590±6 Ma using the LA-ICPMS U-Pb method, whereas monazites from anhydrite-apatite-carbonate rocks show a concordant U-Pb-Th age corresponding to 449 ± 2 Ma. Temperatures inferred fromcalcite-dolomite solvus data and graphite structural ordering span the interval from >=815 to 276 °C. Primary and secondary fluid inclusions in apatite document calciocarbonatite melts associated with early apatite, and CO2-bearing sulfate-chloride brines progressively dilutedwith low-salinity, probably meteoric waters, towards ultimate stages of the deposit formation. The calciocarbonatite melts have initially coexisted with liquid nitrogen and later with sulfate-chloride brines mixed with N2± CO2 gas. Crystallization of spinel around baddeleyite by the mechanismof Ostwald ripening, nucleation of graphite spherules along pyrrhotite-carbonate boundaries, the occurrence of molybdenite, baddeleyite-to-zircon transformation, and high crystallization temperatures inferred from graphite structural ordering and calcite-dolomite thermometry suggest a magmatic origin of the early mineral assemblages. In contrast, microthermometric characteristics of primary aqueous inclusions in the late apatite and the presence of zeolites (thomsonite-Ca, mezolite) is diagnostic of a low-temperature hydrothermal crystallization. Formation of the early magnetite-apatite-forsterite assemblage is thought to be coeval with mafic alkalic intrusions of the Mazerapane Suite superimposed on the granulite facies metamorphism of the Monapo Klippe. The low-temperature, anhydrite-bearing mineralization was associated with the massive circulation of sulfate-rich brines along fractures activated during the Late Cambrian-Ordovician extension. Origin of the sulfate-rich brines may be genetically related either with the magmatic-hydrothermal differentiation, or with the remobilization of crustal evaporites.
Název v anglickém jazyce
New insights into the origin of the Evate apatite-iron oxide-carbonate deposit, Northeastern Mozambique, constrained by mineralogy, textures, thermochronometry, and fluid inclusions
Popis výsledku anglicky
The Evate deposit represents the largest resource of apatite in south-east Africa (155 Mt. ore grading 9.3 wt.% P2O5) accumulated in up to 100 m thick magnetite-carbonate-apatite horizons conformable to the granulitic gneiss of the Monapo Klippe. Baddeleyite and zircon from early iron-oxide (magnetite, geikielite, spinel), apatite- and forsterite-bearing rocks have been dated to 590±6 Ma using the LA-ICPMS U-Pb method, whereas monazites from anhydrite-apatite-carbonate rocks show a concordant U-Pb-Th age corresponding to 449 ± 2 Ma. Temperatures inferred fromcalcite-dolomite solvus data and graphite structural ordering span the interval from >=815 to 276 °C. Primary and secondary fluid inclusions in apatite document calciocarbonatite melts associated with early apatite, and CO2-bearing sulfate-chloride brines progressively dilutedwith low-salinity, probably meteoric waters, towards ultimate stages of the deposit formation. The calciocarbonatite melts have initially coexisted with liquid nitrogen and later with sulfate-chloride brines mixed with N2± CO2 gas. Crystallization of spinel around baddeleyite by the mechanismof Ostwald ripening, nucleation of graphite spherules along pyrrhotite-carbonate boundaries, the occurrence of molybdenite, baddeleyite-to-zircon transformation, and high crystallization temperatures inferred from graphite structural ordering and calcite-dolomite thermometry suggest a magmatic origin of the early mineral assemblages. In contrast, microthermometric characteristics of primary aqueous inclusions in the late apatite and the presence of zeolites (thomsonite-Ca, mezolite) is diagnostic of a low-temperature hydrothermal crystallization. Formation of the early magnetite-apatite-forsterite assemblage is thought to be coeval with mafic alkalic intrusions of the Mazerapane Suite superimposed on the granulite facies metamorphism of the Monapo Klippe. The low-temperature, anhydrite-bearing mineralization was associated with the massive circulation of sulfate-rich brines along fractures activated during the Late Cambrian-Ordovician extension. Origin of the sulfate-rich brines may be genetically related either with the magmatic-hydrothermal differentiation, or with the remobilization of crustal evaporites.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10500 - Earth and related environmental sciences
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Ore geology reviews
ISSN
0169-1368
e-ISSN
—
Svazek periodika
80
Číslo periodika v rámci svazku
January
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
20
Strana od-do
1072-1091
Kód UT WoS článku
000387625800059
EID výsledku v databázi Scopus
—