Unconformity-related U deposits: Recent advances from fluid inclusions and their host minerals (original) (raw)

Metal-rich fluid inclusions provide new insights into unconformity-related U deposits (Athabasca Basin and Basement, Canada)

The Paleoproterozoic Athabasca Basin (Canada) hosts numerous giant unconformity-related uranium deposits. The scope of this study is to establish the pressure, temperature, and composition (P-T-X conditions) of the brines that circulated at the base of the Athabasca Basin and in its crystalline basement before, during and after UO2 deposition. These brines are commonly sampled as fluid inclusions in quartz- and dolomite-cementing veins and breccias associated with alteration and U mineralization. Microthermometry and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) data from five deposits (Rabbit Lake, P-Patch, Eagle Point, Millennium, and Shea Creek) complement previously published data for the McArthur River deposit. In all of the deposits investigated, fluid inclusion salinity is between 25 and 40 wt.% NaCl equiv., with compositions displaying a continuum between a “NaCl-rich brine” end-member (Cl > Na > Ca > Mg > K) and a “CaCl2-rich brine” end-member (Cl > Ca ≈ Mg > Na > K). The CaCl2-rich brine has the highest salinity and shows evidence for halite saturation at the time of trapping. The continuum of compositions between the NaCl-rich brine and the CaCl2-rich brine end-members combined with P-T reconstructions suggest anisothermal mixing of the two brines (NaCl-rich brine, 180 ± 30 °C and 800 ± 400 bars; CaCl2-rich brine, 120 ± 30 °C and 600 ± 300 bars) that occurred under fluctuating pressure conditions (hydrostatic to supra-hydrostatic). However, because the two brines were U bearing and therefore oxidized, brine mixing was probably not the driving force for UO2 deposition. Several scenarios are put forward to account for the Cl-Na-Ca-Mg-K composition of the brines, involving combinations of seawater evaporation, halite dissolution, mixing with a halite-dissolution brine, Mg/Ca exchange by dolomitization, Na/Ca exchange by albitization of plagioclase, Na/K exchange by albitization of K-feldspar, and Mg loss by Mg-rich alteration. Finally, the metal concentrations in the NaCl-rich and CaCl2-rich brines are among the highest recorded compared to present-day sedimentary formation waters and fluid inclusions from basin-hosted base metal deposits (up to 600 ppm U, 3000 ppm Mn, 4000 ppm Zn, 6000 ppm Cu, 8000 ppm Pb, and 10,000 ppm Fe). The CaCl2-rich brine carries up to one order of magnitude more metal than the NaCl-rich brine. Though the exact origin of major cations and metals of the two brines remains uncertain, their contrasting compositions indicate that the two brines had distinct flow paths and fluid-rock interactions. Large-scale circulation of the brines in the Athabasca Basin and Basement was therefore a key parameter for metal mobility (including U) and formation of unconformity-related U deposits.

Brine-rock interaction in the Athabasca basement (McArthur River U deposit, Canada): consequences for fluid chemistry and uranium uptake: Brine-rock interaction and uranium uptake

Terra Nova, 2010

Terra Nova, 22, 303–308, 2010Terra Nova, 22, 303–308, 2010AbstractThe nature of uranium source rocks, transport conditions and deposition processes are still highly controversial for world-class unconformity-related U deposits. This article presents the first detailed chemistry of brines associated with the giant McArthur River U deposit, Canada. LA-ICP-MS analysis of individual fluid inclusions suggests mixing between a Na–Ca–Mg–K–Sr–Ba brine and a Ca–Mg–Na–K–Sr–Ba brine. The brines share a common origin (evaporated seawater) and show evidence for contrasting interaction with basement rocks. The Na-rich brine lost Mg and K in alteration haloes around U ores, while the Ca-rich brine results from Na–Ca exchange and Sr–Ba gain. U concentrations (0.3–530 μg g−1) are anomalously high compared with usual basinal fluids, this indicating that U uptake occurred within basement rocks. The two brine end-members have mixed within the main U deposit area, which could be one of the major driving forces for U deposition.The nature of uranium source rocks, transport conditions and deposition processes are still highly controversial for world-class unconformity-related U deposits. This article presents the first detailed chemistry of brines associated with the giant McArthur River U deposit, Canada. LA-ICP-MS analysis of individual fluid inclusions suggests mixing between a Na–Ca–Mg–K–Sr–Ba brine and a Ca–Mg–Na–K–Sr–Ba brine. The brines share a common origin (evaporated seawater) and show evidence for contrasting interaction with basement rocks. The Na-rich brine lost Mg and K in alteration haloes around U ores, while the Ca-rich brine results from Na–Ca exchange and Sr–Ba gain. U concentrations (0.3–530 μg g−1) are anomalously high compared with usual basinal fluids, this indicating that U uptake occurred within basement rocks. The two brine end-members have mixed within the main U deposit area, which could be one of the major driving forces for U deposition.

Geochronology of the Paleoproterozoic basement-hosted unconformity-type uranium deposits in Northern Saskatchewan, Canada

Mineralium Deposita, 2009

The importance of geochronology in the study of mineral deposits in general, and of unconformity-type uranium deposits in particular, resides in the possibility to situate the critical ore-related processes in the context of the evolution of the physical and chemical conditions in the studied area. The present paper gives the results of laser step heating 40Ar/39Ar dating of metamorphic host-rock minerals, pre-ore and syn-ore alteration clay minerals, and laser ablation inductively coupled plasma mass spectrometer (LA-ICP-MS) U/Pb dating of uraninite from a number of basement- and sediment-hosted unconformity-related deposits in the Athabasca Basin, Canada. Post-peak metamorphic cooling during the Trans-Hudson Orogen of rocks from the basement occurred at ca 1,750 Ma and gives a maximum age for the formation of the overlying Athabasca Basin. Pre-ore alteration occurred simultaneously in both basement- and sandstone-hosted mineralizations at ca 1,675 Ma, as indicated by the 40Ar/39Ar dating of preore alteration illite and chlorite. The uranium mineralization age is ca 1,590 Ma, given by LA-ICP-MS U/Pb dating of uraninite and 40Ar/39Ar dating of syn-ore illite, and is the same throughout the basin and in both basement- and sandstone-hosted deposits. The mineralization event, older than previously proposed, as well as several fluid circulation events that subsequently affected all minerals studied probably correspond to far-field, continent-wide tectonic events such as the metamorphic events in Wyoming and the Mazatzal Orogeny (ca 1.6 to 1.5 Ga), the Berthoud Orogeny (ca 1.4 Ga), the emplacement of the McKenzie mafic dyke swarms (ca 1.27 Ga), the Grenville Orogeny (ca 1.15 to 1 Ga), and the assemblage and break-up of Rodinia (ca 1 to 0.85 Ga). The results of the present work underline the importance of basin evolution between ca 1.75 Ga (basin formation) and ca 1.59 Ga (ore deposition) for understanding the conditions necessary for the formation of unconformity-type uranium deposits.