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The Neoproterozoic (840 Ma) Sin Quyen deposit in northwestern Vietnam contains replacement Cu-LREE-Au orebodies in Proterozoic metasedimentary rocks. In this deposit, LREE-bearing minerals include allanite-(Ce), monazite-(Ce), chevkinite-(Ce), and fluorapatite. Fluorapatite from orebodies has undergone variable degrees of metasomatic alteration. Samarium-neodymium isotopic analyses were conducted on altered fluorapatite, and also on allanite-(Ce) and monazite-(Ce), to investigate whether such metasomatism can affect the Sm-Nd isotope system. Allanite-(Ce) and monazite-(Ce) have 147Sm/144Nd ratios ranging from 0.0359 to 0.0549, and 143Nd/144Nd ratios from 0.51147 to 0.51172. Their initial 143Nd/144Nd values at the time of mineralization range from 0.51126 to 0.51148, but mostly cluster between 0.51135 and 0.51145. Thus, the primary ore-forming fluids were relatively homogeneous in their Sm-Nd isotopic compositions. In the 147Sm/144Nd vs. 143Nd/144Nd diagram, the compositions of allanite-(Ce) and monazite-(Ce) generally plot along a Sm-Nd isochron of 840 Ma, implying that the Sm-Nd isotopic systems of these minerals were either closed or only slightly modified. In contrast, altered fluorapatite crystals have 147Sm/144Nd ratios varying from 0.0667 to 0.1348, and 143Nd/144Nd ratios from 0.51160 to 0.51199. The calculated initial 143Nd/144Nd ratios range widely from 0.51114 to 0.51141, with most values lower than those of the allanite-(Ce) and monazite-(Ce). In the 147Sm/144Nd vs. 143Nd/144Nd diagram, their compositions mostly plot below the 840-Ma Sm-Nd isochron. Petrographic observations and trace elemental analyses show that metasomatic modification of fluorapatite grains led to increases of their Sm/Nd ratios. The unaltered domains in the grains have Sm/Nd ratios varying from 0.114 to 0.200, with an average value of 0.161; whereas the altered domains have Sm/Nd ratios varying from 0.111 to 0.254, with an average value of 0.183. The increased Sm/Nd ratios can cause the calculated initial 143Nd/144Nd ratios to be lower than actual initial isotopic ratios, and can also result in compositional deviations from the reference Sm-Nd isochron. This study demonstrates that the traditionally assumed inert Sm-Nd isotopic system can be metasomatically disturbed due to changes in the Sm/Nd ratio. Therefore, care must be taken when interpreting the Sm-Nd isotopic data from apatite/apatite-rich rocks that have undergone metasomatic alteration. [ABSTRACT FROM AUTHOR]

The Sin Quyen deposit in northwestern Vietnam is composed of Fe-Cu-LREE-Au ore bodies hosted in Proterozoic metapelite. There are massive and banded replacement ores with variable amounts of monazite-(Ce) and chevkinite-(Ce) crystals, which have undergone fluid-induced alteration. Monazite-(Ce) and chevkinite-(Ce) were deposited from high-temperature fluids in the early ore-forming stage, but became thermodynamically unstable, and thus were altered to other phases in later ore-forming stages. The alteration of monazite-(Ce) formed a three-layered corona texture, which commonly has relict monazite-(Ce) in the core, newly formed fluorapatite in the mantle, and newly formed allanite-(Ce) in the rim. In some cases, the original monazite-(Ce) was completely consumed, forming a core of polygonal fluorapatite crystals rimmed by allanite-(Ce) crystals. The formation of allanite-(Ce) and fluorapatite at the expense of monazite-(Ce) indicates that the later-stage fluids had high Ca/Na ratios and relatively low temperatures. Chevkinite-(Ce) was variably replaced by an assemblage of allanite-(Ce) + aeschynite-(Ce) ± bastnäsite-(Ce) ± columbite-(Fe) ± ilmenite. The replacement of chevkinite-(Ce) by mainly allanite-(Ce) and aeschynite-(Ce) required low-temperature, Ca-, LREE-, and Nb-rich metasomatic fluids, probably with relatively low fO2. Mass-balance calculations were made to investigate the hydrothermal element mobility. It is assumed that Th was immobile during the alteration process of monazite-(Ce). Light (and middle) REE from La to Tb, U, As, and Ge were variably lost relative to Th, while heavy REE from Dy to Lu, HFSE (e.g., Nb, Ta, Zr, and Hf) and Sr were variably gained relative to Th. Regarding the alteration of chevkinite-(Ce), some major elements in chevkinite-(Ce), such as Ti, La, and Ce, were obviously removed from the system during alteration, whereas Ca, Al, Nb, U, and HREE were needed to be variably supplied by the metasomatic fluids. Concerning the hydrothermal mobility of trace elements, previous studies demonstrated that REE and HFSE can be commonly reserved in the system during alteration, consistent with the traditionally assumed immobile nature of these elements. In contrast, this study shows that REE and HFSE can be mobilized on at least the hundreds of micrometers scale. This may be related to the high flux and strong chemical reactivity of the metasomatic fluids. [ABSTRACT FROM AUTHOR]