Bartosz Budzyń

Experimental determination of stability relations between monazite, fluorapatite, allanite, and REE-epidote as a function of pressure, temperature, and fluid composition

Abstract The experimental alteration of monazite to allanite, REE-epidote, fluorapatite, and/or fluorapatitebritholite was investigated at 450 to 610 MPa and 450 to 500 °C. Experiments involved monazite + albite ± K-feldspar + muscovite ± biotite + SiO2 + CaF2 and variety of fluids including H2O, (KCl + H2O), (NaCl + H2O), (CaCl2 + H2O), (Na2Si2O5 + H2O), 1 M HCl, 2 M NaOH, 2 M KOH, 1 M Ca(OH)2, 2 M Ca(OH)2, and (CaCO3 + H2O). The reaction products, or lack thereof, clearly show that the stability relations between monazite, fluorapatite, and allanite or REE-epidote are more dependent on the fluid composition and the ratio of silicate minerals than on the P-T conditions. A high Ca content in the fluid promotes monazite dissolution and the formation of fluorapatite and allanite or REE-epidote. Lowering the Ca content and raising the Na content in the fluid decreases the solubility of monazite but promotes the formation of allanite. Replacing Na with K in the same fluid causes fluorapatite, with a britholite component, to form from the monazite. However, allanite and REE-epidote are not formed. Monazite is stable in the presence of NaCl brines. In KCl brine, monazite shows a very limited reaction to fluorapatite. When the fluid is (Na2Si2O5 + H2O), strong dissolution of monazite occurs resulting in the mobilization of REEs, and actinides to form fluorapatite-britholite and turkestanite. These experimental results are consistent with natural observations of the partial to total replacement of monazite by fluorapatite, REE-epidote, and allanite in fluid-aided reactions involving the anorthite component in plagioclase at mid- to high-grade metamorphic conditions. In contrast, an alkali-bearing environment with excess Na prevents the growth of allanite and eventually promotes the precipitation of secondary monazite. The results from this study provide implications for geochronology and for deducing fluid compositions in metamorphic rocks.

Sensitive high-resolution ion microprobe analysis of zircon reequilibrated by late magmatic fluids in a hybridized pluton

Zircon from a microgranular enclave in the ca. 315 Ma postcollisional Karkonosze pluton (Western Sudetes, northeastern Bohemian Massif) is characterized by unusual morphologies and reequilibration textures. Blocky, clustered, and skeletal Th-U–rich zircon grains are internally corroded along discrete boundary zones, and subsequently replaced by porous microgranular aggregates of zircon and various other minerals, including thorite. The boundary zones have textures and compositions characteristic of diffusion-controlled chemical reaction fronts, including enrichment in Ca, Ba, and light rare earth elements, whereas microgranular domains are typical of zircon replacement and regrowth by coupled dissolution and precipitation. Initial zircon crystallization occurred with the mingling of mafic magma into a cooler granitic melt, whereas zircon modification is attributed to the reaction of late magmatic fluids from the host granite with the enclave. Precise dating of reequilibrated zircon as 304 ± 2 Ma indicates that fluid activity, which is also responsible for scheelite mineralization, postdates the emplacement of the main part of the pluton by several millions of years.

Fluid–mineral interactions and constraints on monazite alteration during metamorphism

Abstract Clasts of metamorphosed Cadomian granites from the ~50−60 Ma Carpathian flysch in Gródek near the Rożnowskie Lake (Silesian Unit, SE Poland) are studied. They are considered to represent the Silesian Ridge, one of the hypothetical, currently unexposed source areas that supplied Carpathian sedimentary basins with clastic material. The gneisses preserve several examples of corona textures that include cores of primary monazite surrounded by polygonal grains of secondary apatite with thorianite inclusions, with intermediate zones of lamellar grains of secondary monazite and outermost rims of clay minerals, or various combinations thereof. Preservation of the complete textures is rare with polygonal apatite with thorianite inclusions, lamellar grains of monazite and clay minerals being particularly prevalent. Locally, polygonal apatite with thorianite inclusions surrounded by allanite and REE-epidote corona with a bastnäsite-synchysite phase occurs also. The textures observed developed during primary monazite breakdown and replacement by secondary minerals. The variation in reaction products indicates that alteration was strictly dependent on the local chemical system.

Monazite Breakdown in Metapelites From Wedel Jarlsberg Land, Svalbard — Preliminary Report

Monazite Breakdown in Metapelites From Wedel Jarlsberg Land, Svalbard — Preliminary Report Metapelites from the SW part of Wedel Jarlsberg Land were progressively metamorphosed under amphibolite facies conditions followed by a Caledonian low-temperature metamorphic event under greenschist facies conditions. The latter resulted in various stages of monazite breakdown. These include monazite alterations and the formation of allanite-apatite coronas.

Fluorapatite-hingganite-(Y) coronas as products of fluid-induced xenotime-(Y) breakdown in the Skoddefjellet pegmatite, Svalbard

Abstract The pre-Caledonian NYF Skoddefjellet pegmatite in Wedel Jarlsberg Land, Svalbard, contains xenotime-(Y) that is partly replaced by fluorapatite-hingganite-(Y) reaction coronas. Hingganite-(Y) contains up to 2.0 wt.% of Gd2O3, 4.7 wt.% of Dy2O3, 3.3 wt.% of Er2O3 and 5.5 wt.% of Yb2O3. Such unusual, previously undescribed, xenotime-(Y) breakdown was caused by Ca- and F-bearing fluids interacting with the pegmatite. The occurrence of hinnganite-(Y) as a breakdown product of xenotime-(Y) implies that a Be-bearing phase (beryl in this case) was also involved in the reaction. There are few Ca-bearing primary phases in the pegmatite, indicating that the source of fluid was probably located in the generally Ca-richer host rocks (metasediments), though the fluid composition was modified during metasomatism of the pegmatite (i.e. beryl dissolution).