The Zoovch Ovoo uranium deposit is located in East Gobi Basin in Mongolia. It is hosted in the Sainshand Formation, a Late Cretaceous siliciclastic reservoir, in the lower part of the post-rift infilling of the Mesozoic East Gobi Basin. The Sainshand Formation corresponds to poorly consolidated medium-grained sandy intervals and clay layers deposited in fluvial-lacustrine settings. The uranium deposit is confined within a 60- to 80-m-thick siliciclastic reservoir inside aquifer driven systems, assimilated to roll-fronts. As assessed by vitrinite reflectance (%Rr < 0.4) and molecular geochemistry, the formation has never experienced significant thermal maturation. Detrital organic matter (type III and IV kerogens) is abundant in the Zoovch Ovoo depocenter. In this framework, uranium occurs as: (i) U-rich macerals without any distinguishable U-phase under SEM observation, containing up to 40 wt % U; (ii) U expressed as UO2 at the rims of large (several millimeters) macerals and (iii) U oxides partially to entirely replacing macerals, while preserving the inherited plant texture. Thus, uranium is accumulated gradually in the macerals through an organic carbon–uranium epigenization process, in respect to the maceral’s chemistry and permeability. Most macerals are rich in S and, to a lesser extent, in Fe. Frequently, Fe and S contents do not fit the stoichiometry of pyrite, although pyrite also occurs as small inclusions within the macerals. The organic matter appears thus as a major redox trap for uranium in this kind of geological setting.

Shallow buried unconsolidated sands generally provide very little information about diagenesis as most detrital minerals remain unchanged. However, in rare cases carbonate cemented nodules or sandstone layers may occur inside unconsolidated series. These cements could help to reconstruct the chronology of events from early to late phase stages of diagenesis. The Late Cretaceous sequence of the Zoovch Ovoo depocenter in East Gobi Basin is represented by 600m of clastic deposits. The 60-80m of Cenomanian unconsolidated sands and clays, deposited in alluvial-deltaic to lacustrine settings, compose the upper part of the post-rift medium-grained siliciclastic reservoir, the Sainshand Formation which hosts uranium roll-front systems. Dolomite cemented sandstone layers with 10-20cm thickness occur among the unconsolidated rock facies. Calcite is absent from this formation, but is present only in the overlying, also outcropping, Bayanshiree Formation. Samples from the dolomite cemented sandstone layers were investigated in detail to uncover their origin and diagenetic history. Four dolomite cement types were recognized that indicate recrystallization episodes and were classified based on the size and shape of the crystals, namely: (i) microcrystalline dolomite frequently associated with siderite, (ii) euhedral dolomite also associated with siderite, (iii) subhedral dolomite and (iv) finally anhedral dolomite. Their REE content varies significantly from dolomite I to IV, in particular by a strong depletion in LREE about 30 times. The contrasted precipitation of calcite in Bayanshiree and dolomite cements in Sainshand formations could be attributed to different Mg/Ca ratio of the circulation fluids in the two aquifers. Both carbonates display however rather homogenous oxygen and carbon isotopic compositions for δ 18 O (-10±1‰ V-PDB) and δ 13 C (-7±1‰ V-PDB). The δ 18 O values are interpreted as inherited from typical meteoric waters quite close to present day waters. The δ 13 C values indicate a mixed source of both organic and mineral carbon. All data taken into account, a full paragenetic succession was constructed. It includes the evolution of dolomite during burial diagenesis and the effects of the oxidizing roll-front uranium rich waters in the system. The latter induces partial dissolution followed by precipitation of a dolomite phase typical of roll-front zones. Carbonate cements can be thus considered as the best and rather unique geochemical indicators for the recognition of a burial history framework to paleofluid circulations and fluid-rock interactions in these intracontinental series of unconsolidated sands.

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The main objective of this paper is to study by means of Organic Petrology techniques, the maturity of the dispersed organic matter from certain sedimentary formations of the Ionian Zone, such as the Bituminous Shale, the Upper Siliceous

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The Zoovch Ovoo uranium roll-front-type deposit is hosted in the Sainshand Formation, a Late Cretaceous siliciclastic reservoir, which constitutes the upper part of the post-rift infilling of the Mesozoic East Gobi Basin in SE Mongolia. The Sainshand Formation consists of unconsolidated medium-grained sand, silt and clay intervals deposited in fluvial-lacustrine settings. The uranium deposit is confined within a 60-80 m thick siliciclastic sequence inside aquifer-driven systems. The overall system experienced shallow burial and was never subjected to temperatures higher than 40°C. This study proposes a comprehensive metallogenic model for this uranium deposit. Sedimentological and mineralogical observations from drill core samples to the microscopic scale (optical and Scanning Electron Microscopy) together with in situ geochemistry of late-formed phases (Laser Ablation-Inductively Coupled Plasma Mass Spectrometry, Electron Probe Microanalysis, Fourier Transform-Infrared Spectroscopy) were considered for the reconstruction of the main stages of U trapping.In the mineralized zone, the uranium ore is expressed as Ca-enriched uraninite (UO 2 ) and less commonly as Ca-enriched phospho-coffinite (U, P)SiO 4 . Trapping mechanisms include i) complexation (i.e. uranyl-carboxyl complexes), ii) adsorption on organic or clay particles) and iii) reduction by pyrite and by bacterial activity to amorphous uraninite. In all cases, the organic matter plays either the role of trap for uranium or nutrient for bacteria that can trap uranium through their metabolism. The shallow burial diagenesis conditions do not allow direct reduction of U(VI) by organic carbon. The δ 34 S values of the iron disulfide are very diverse, fluctuating in extreme cases between -50 to +50‰, with an average δ 34 S value for framboidal pyrite at 2‰, and -20‰ for euhedral pyrite. The positive and negative values reflect close versus open fractionation systems, while bacterial sulphate reduction (BSR) is active during the whole diagenetic history of the deposit as an essential source of reduced sulfur. Therefore, using detrital organic matter as a carbon source, microorganisms play a significant role in uranium trapping, either as a direct reducing agent for uranium or pyrite formation, which will trap uranium redox driven epigenetic processes.