Occurrence and paragenesis of diagenetic monazite in the upper Triassic black shales of the Marvast region, South Yazd, Iran

Upper Triassic-Jurassic black shale at Marvast, Iran, contains grey to green-grey ellipsoidal nodules of monazite ranging from 0.1 to 2?mm across. The presence of host-rock mineral inclusions within the monazite grains, low Th content in the monazite, lack of relict yellow cores (characteristic of igneous monazite), and the absence of monazite in the other sedimentary sequences in the Marvast area rule out a detrital origin for the monazite nodules and suggest authigenic crystallization during sediment compaction. Enrichment of the cores of the monazite grains in mid-range to heavy rare-earth elements (REE) and their rims in La + Ce point to variations in the degree of REE mobility and/or evolving composition of the diagenetic mineralizing fluid during nodule growth. The phosphorus and REE required for monazite crystallization were probably derived from seawater and adsorbed on clays and Fe-Mn hydroxides. The interstitial fluids expelled from the sediments during burial compaction and diagenesis became enriched in P and REE through complexing. The association of the Marvast monazite nodules with the black shale may indicate that organic complexes aided in the mobilization and transport of the REE into the pore fluids. Detailed field investigations in the study area and vicinity show that authigenic monazite in the upper Triassic-Jurassic shale sections is spatially associated with quartz lenses. It is likely that these lenses are surface expressions of shallow intrusive magmas, which provided the heat that promoted the mobilization and redistribution of the REE and P, and initiated precipitation of monazite in the overlying sediments.     

Trace-element distributions in silicates during prograde metamorphic reactions: implications for monazite formation

To assess the petrogenetic relationship between monazite and major silicates during prograde metamorphism, REE were measured across coexisting zoned silicates in garnet through kyanite‐grade pelitic schists from the Great Smoky Mountains, western Blue Ridge terrane, southern Appalachians, to establish REE concentrations and distributions before and after the monazite‐in isograd, and to identify the role major silicates play in the formation of monazite. Results indicate significant scavenging of light rare‐earth elements (LREE) from silicates during the monazite‐in isograd reaction; however, the absolute concentration of LREE hosted in the silicates was insufficient to produce monazite in the quantity observed in these schists. Monazite must have formed mainly from either the dissolution of allanite or some other source of concentrated LREE (possibly adsorbed onto grain boundaries), even though direct evidence for allanite is lacking in a majority of the samples. Laser‐ablation ICP‐MS analyses and theoretical thermodynamic calculations show that monazite may have formed as a result of contributions from both allanite and major silicates. Allanite breakdown initially formed monazite, and monazite production drew LREE liberated from allanite, major silicates and possibly from crystal boundaries. In many rocks the reaction was further promoted by the staurolite‐in reaction, allowing for rapid, isogradic monazite growth.     

Thermobarometric modelling of zircon and monazite growth in melt-bearing systems: examples using model metapelitic and metapsammitic granulites

U–Pb age data collected from zircon and monazite are used to draw fundamental inferences about tectonic processes in the Earth. Despite the emphasis placed on zircon and monazite ages, the understanding of how to relate the timing of growth of zircon and monazite to an evolving rock system remains in its infancy. In addition, few studies have presented large datasets of geochronological data from zircon and monazite occurring in the same metamorphic rock sample. Such information is crucial for understanding the growth of zircon relative to monazite in a systematic and predictive manner, as per this study. The data that exist support the generally held conception that zircon ages tend to be older than monazite ages within the same rock. Here experimental data for zircon and monazite saturation in melt-bearing rocks are integrated with phase diagram calculations. The calculations constrain the dissolution and growth behaviour of zircon and monazite with respect to evolving pressure, temperature and silicate mineral assemblages in high-grade, melt-bearing, metasedimentary rocks. Several key results emerge from this modelling: first, that in aluminous metapelitic rocks (i.e. garnet + cordierite + sillimanite assemblages), zircon ages are older than monazite ages in the same rock; second, that the growth rate of accessory minerals is nonlinear and much higher at and near saturation than at lower temperatures; and third, that the difference in zircon and monazite ages from the same rock may be ascribed to differences in the temperature(s) at which zircon and monazite grow rather than differences in closure temperature systematics. Using our methodology the cooling rate of granulites from the Reynolds Range, central Australia, have been constrained at ∼4 °C Myr⁻¹. This study serves as a first-pass template on which further research in applying the technique to a field study can be based.     

Microcrystals of Th-rich monazite (La) with a negative Ce anomaly in metadiorite and their role for documenting Cretaceous metamorphism in the Slavonian Mountains (Croatia)

Microcrystals (1–15 μm) of unusual monazite (La) with 41–47 mol% cheralite [ThCa(PO₄)₂] component and a strong negative Ce anomaly are described from a metadiorite from the SW Slavonian Mountains, Psunj, Croatia. The dioritic host rock still shows a relictic igneous fabric on macroscopic scale. However, metamorphic reaction textures can be recognized in thin section. These include partial recrystallization of igneous plagioclase to albite coupled with the formation of epidote. Furthermore, partial replacement of igneous hornblende by a fine-grained orthoamphibole-chamosite-epidote paragenesis can be observed and replacement of ilmenite by titanite. The compositions of the metamorphic minerals indicate upper greenschist facies conditions (460–500 °C according to two-feldspar geothermometry) under a high oxygen fugacity. Microstructures show that the monazite crystals belong to the metamorphic paragenesis and formed at the expense of magmatic allanite. Their negative Ce anomalies reflect the oxidizing conditions of metamorphism. Application of the xenotime in monazite solvus geothermometer provides unrealistically high temperatures of ~500–660 °C which disagree with the greenschist facies metamorphic paragenesis. We interpret that the presence of cheralite has a profound effect on the nature of the monazite-xenotime solvus curve and hence the existing calibrations of this geothermometer may be generally unsuitable for cheralite-rich monazite. An important geological result is that the Th-U-total Pb ages of the monazite grains are uniformingly Upper Cretaceous. Our data thus suggest that the imprint of the Alpine orogeny on the Slavonian Mountains was stronger than presumed until now.     

Age constraints on Late Paleozoic evolution of continental crust from electron microprobe dating of monazite in the Peloritani Mountains (southern Italy): another example of resetting of monazite ages in high-grade rocks

In situ monazite microprobe dating has been performed, for the first time, on trondhjemite and amphibolite facies metasediments from the Peloritani Mountains in order to obtain information about the age of metamorphism and intrusive magmatism within this still poorly known sector of the Hercynian Belt. All samples show single-stage monazite growth of Hercynian age. One migmatite and one biotitic paragneiss yielded monazite ages of 311 ± 4 and 298 ± 6 Ma, respectively. These ages fit with previous age determinations in similar rocks from southern Calabria, indicating a thermal metamorphic peak at about 300 Ma, at the same time as widespread granitoid magmatism. The older of the two ages might represent a slightly earlier event, possibly associated with the emplacement of an adjacent trondhjemite pluton, previously dated by SHRIMP at 314 Ma. No evidence for pre-Hercynian events and only a little indication for some monazite crystallization starting from ca. 360 Ma were obtained from monazite dating of the metasediments, suggesting either a single-stage metamorphic evolution or a significant resetting of the monazite isotope system during the main Hercynian event (ca. 300 Ma). Rare monazite from a trondhjemite sample yields evidence for a late-Hercynian age of about 275 Ma. This age is interpreted as representing a post-magmatic stage of metasomatic monazite crystallization, which significantly postdates the emplacement of the original magmatic body.     

Conventional and in situ geochronology of the Teplá Crystalline unit, Bohemian Massif: implications for the processes involving monazite formation

The Teplá Crystalline unit (TCU), western Bohemian Massif, proves highly suitable for studying the effects of differential metamorphic reworking on the U–Th–Pb systematics in monazite, as the overprint of Variscan regional metamorphism onto high-grade Cadomian paragneisses intensifies progressively towards the northwest. Although variably hampered by scarcity, small size, and low uranium contents of monazite, isotope dilution–thermal ionisation mass spectrometry of monazite from paragneisses from the garnet, staurolite, and kyanite zones of the TCU gives a narrow ²⁰⁶Pb/²³⁸U age range from 387 to 382 Ma for Variscan peak metamorphism. These data are supported by 382–373 Ma monazite ages derived from electron microprobe analyses. Inheritance of older components in grains from the central TCU imply major “resetting” of pre-Variscan monazite around 380 Ma, possibly due to widespread garnet growth during Variscan metamorphism, which led to the consumption of pre-Variscan high-Y monazite and subsequent growth of new low-Y monazite. Concordant 498–494 Ma monazite ages in a migmatitic paragneiss close to the adjacent Mariánské Lázně Complex (MLC) grew in response to metagabbro emplacement in the MLC from 503 to 496 Ma and not during either Cadomian or Variscan regional metamorphism. Backscatter imaging and electron microprobe analyses reveal that discordant monazite of the migmatite comprises a mix of various age domains that range from ca. 540 to 380 Ma. Combined evidence presented here suggests that instead of Pb loss by volume diffusion, the apparent resetting of the U–Th–Pb systematics in monazite rather involves new crystal growth or regrowth by recrystallisation and dissolution/reprecipitation.     

Age trends in garnet-hosted monazite inclusions from upper amphibolite facies schist in the northern Grouse Creek Mountains, Utah

We performed in situ Th-Pb dating of monazite in upper amphibolite facies pelitic schist from the Grouse Creek Mountains in northwest Utah. Sixty-six ages from inclusions in four garnet grains range from 37 to 72 Ma and decrease with radial distance from garnet cores. The age range of 30 matrix monazite grains overlaps and extends to younger ages than inclusions (25-58 Ma). The monazite grains are not intersected by cracks in the garnets, through which dissolution, reprecipitation or Pb loss might occur, and are generally too small (<20 μm) to allow for more than one age determination on any one grain. Processes that might explain inclusion ages that decrease with radial distance from garnet cores include: (1) Pb diffusion in monazite, (2) dissolution and reprecipitation of monazite, and (3) co-crystallization of monazite and garnet. After consideration of these possibilities, it is concluded that the co-crystallization of monazite and garnet is the most plausible, with monazite neoblasts deriving REEs from the breakdown of muscovite. Garnet ages derived by regression of the inclusion ages and assuming a constant rate of volume increase during garnet growth yield model ages with a maximum difference between core and rim of 22 m.y.     

Formation of monazite and xenotime inclusions in fluorapatite megacrysts, Gloserheia Granite Pegmatite, Froland, Bamble Sector, southern Norway

Xenotime and monazite inclusions in fluorapatite megacrysts from a granitic pegmatite, Gloserheia, Froland, Bamble Sector, southern Norway are described utilizing high contrast backscattered electron imaging of cross sections of a selection of fluorapatite crystals. Electron microprobe analysis is then used to further characterize the xenotime and monazite, as well as (Y+REE) normal and depleted regions in the fluorapatite. In the (Y+REE) normal regions Y₂O₃ ranges from 0.4 to 1.3 whereas it ranges from below the electron microprobe detection limit to around 0.4 in the depleted regions. Low Y values in monazite (X_Y?=?0.01?0.05) co-existing with xenotime indicates that inclusion formation in the originally (Y+REE)-enriched fluorapatite must have occurred below 300°C. Formation of the xenotime and monazite inclusions is attributed to fluid-aided coupled dissolution-reprecipitation processes during the later stages of subsolidus cooling of the pegmatite. The fluorapatite megacrysts are hypothesized to have under gone two major fluid-induced alteration events. The first occurred sometime after crystallization was complete at temperatures below 300°C and resulted in the initial formation of the xenotime and monazite inclusions. The second occurred at some later time as the product of a relatively limited fluid infiltration, also under T?<?300°C. This resulted in the formation of (Y+REE)-depleted regions along lattice and cleavage planes while at the same time promoting Ostwald ripening of the xenotime inclusions resulting in larger grains in the (Y+REE)-depleted areas.     

Genesis of monazite and Y zoning in garnet from the Black Hills, South Dakota

The paragenesis of monazite in metapelitic rocks from the contact aureole of the Harney Peak Granite, Black Hills, South Dakota, was investigated using zoning patterns of monazite and garnet, electron microprobe dating of monazite, bulk-rock compositions, and major phase mineral equilibria. The area is characterized by low-pressure and high-temperature metamorphism with metamorphic zones ranging from garnet to sillimanite zones. Garnet porphyroblasts containing euhedral Y annuli are observed from the garnet to sillimanite zones. Although major phase mineral equilibria predict resorption of garnet at the staurolite isograd and regrowth at the andalusite isograd, textural and mass balance analyses suggest that the formation of the Y annuli is not related to the resorption-and-regrowth of garnet having formed instead during garnet growth in the garnet zone. Monazite grains in Black Hills pelites were divided into two generations on the basis of zoning patterns of Y and U: monazite 1 with low-Y and -U and monazite 2 with high-Y and -U. Monazite 1 occurs in the garnet zone and persists into the sillimanite zone as cores shielded by monazite 2 which starts to form in the andalusite zone. Pelites containing garnet porphyroblasts with Y annuli and monazite 1 with patchy Th zoning are more calcic than those with garnet with no Y annuli and monazite with concentric Th zoning. Monazite 1 is attributed to breakdown of allanite in the garnet zone, additionally giving rise to the Y annuli observed in garnet. Monazite 2 grows in the andalusite zone, probably at the expense of garnet and monazite 1 in the andalusite and sillimanite zones. The ages of the two different generations of monazite are within the precision of chemical dating of electron microprobe. The electron microprobe ages of all monazites from the Black Hills show a single ca. 1713 Ma population, close to the intrusion age of the Harney Peak Granite (1715 Ma). This study demonstrates that Y zoning in garnet and monazite are critical to the interpretation of monazite petrogenesis and therefore monazite ages.     

Sulfur-rich monazite with high common Pb in ore-bearing schists from the Schellgaden mining district (Tauern Window, Eastern Alps)

The compositional variation of accessory monazite in ore bearing micaschists from the Schellgaden mining district, Tauern Window, Eastern Alps, was studied by means of the electron microprobe. In ore-rich domains monazite yields unusually high sulfur contents (up to 2.5?wt.% SO₃), which enter the monazite structure together with Ca and Sr as ??anhydrite-celestine?? component replacing P and REEs. The exchange reaction is S⁶⁺+ (Ca, Sr)²⁺ = REE³⁺+ P⁵⁺. Sulfur-rich monazite is intergrown with anglesite, pyromorphite or galena and shows oscillatory zoning indicating growth from S-bearing fluids. This type of S-enriched monazite yields very high common lead contents (up to 0.5?wt.% PbO) and unrealistic high apparent Th-U-total Pb single dates (> 1?Ga). However, S-enriched monazite grains provide a flat trendline in the Th* vs. Pb isochron diagram similar to the trendline defined through low-S, and low-Pb monazite crystals (0.1?C1?wt.% SO₃, < 0.05?wt.% PbO), which were observed in ore-poor parts of micaschists. Results from this study imply an Alpine rather than a pre-Alpine formation age for monazite and a strong S-rich fluid activity during the Alpine orogeny. Apart from this geological aspect, the current study also shows that the detection of sulfur in monazite may serve as a warning for a possible presence of common Pb.     

Monazite in Hydrothermal Veins from Alinci,Yugoslavia

Summary A new occurrence of monazite from Alinci, SE Yugoslavia, is described. Crystal morphology studies showed that crystals possess a platelike habit on T01 which we regard as a hitherto unknown morphological feature of monazite. The material has been analysed for uranium, thorium and rare earth element content using gamma spectrometry and inductively coupled argon-plasma atomic emission spectrometry (ICPAES). The monazite displays a complex chemical composition, essentially given as (REE+Y,Th,U,Fe)_1.001P_0.988O₄. The infrared absorption spectra and X-ray diffraction data are in agreement with those for terrestrial monazite, although they indicate minor structural variations caused by the REE distribution in the Alinci monazite.

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Monazit aus hydrothermalen Gängen von Alinci, Jugoslawien

Zusammenfassung Es wird ein neues Monazitvorkommen von Alinci, Jugoslawien, beschrieben. Kristallmorphologische Studien zeigten, daß die Kristalle einen plattigen Habitus nach (T01) aufweisen, eine nach Wissen der Autoren bisher unbekannte morphologische Erscheinung bei Monazit. Das Material wurde auf die Uran-, Thorium- und Seltenerdgehalte mit Gamma-Spektrometrie und induktiv gekoppelter Argonplasma-Atomabsorptions-Spektrometrie (ICPAES) analysiert. Der Monazit zeigt eine komplexe chemische Zusammensetzung, die im wesentlichen als (REE+Y,Th,U,Fe)_1.001P_0.988O₄ angegeben werden kann. Die Ultrarotspektren und die Röntgenbeugungs-Daten stimmen mit jenen von terrestrischem Monazit überein, obwohl sie kleine strukturelle Variationen anzeigen, die durch die REE-Verteilung im Monazit von Alinci verursacht sind.

     

Pressure and temperature conditions for crystallization of metamorphic allanite and monazite in metapelites: a case study from the Miyar Valley (high Himalayan Crystalline of Zanskar,NW India)

The textural and chemical evolution of allanite and monazite along a well‐constrained prograde metamorphic suite in the High Himalayan Crystalline of Zanskar was investigated to determine the P–T conditions for the crystallization of these two REE accessory phases. The results of this study reveals that: (i) allanite is the stable REE accessory phase in the biotite and garnet zone and (ii) allanite disappears at the staurolite‐in isograd, simultaneously with the occurrence of the first metamorphic monazite. Both monazite and allanite occur as inclusions in staurolite, indicating that the breakdown of allanite and the formation of monazite proceeded during staurolite crystallization. Staurolite growth modelling indicates that staurolite crystallized between 580 and 610 °C, thus setting the lower temperature limit for the monazite‐forming reaction at ~600 °C. Preservation of allanite and monazite inclusions in garnet (core and rim) constrains the garnet molar composition when the first monazite was overgrown and subsequently encompassed by the garnet crystallization front. Garnet growth modelling and the intersection of isopleths reveal that the monazite closest to the garnet core was overgrown by the garnet advancing crystallization front at 590 °C, which establishes an upper temperature limit for monazite crystallization. Significantly, the substitution of allanite by monazite occurs in close spatial proximity, i.e. at similar P–T conditions, in all rock types investigated, from Al‐rich metapelites to more psammitic metasedimentary rocks. This indicates that major silicate phases, such as staurolite and garnet, do not play a significant role in the monazite‐forming reaction. Our data show that the occurrence of the first metamorphic monazite in these rocks was mainly determined by the P–T conditions, not by bulk chemical composition. In Barrovian terranes, dating prograde monazite in metapelites thus means constraining the time when these rocks reached the 600 °C isotherm.     

Five generations of monazite in Langtang gneisses: implications for chronology of the Himalayan metamorphic core

Monazite grains from Greater Himalayan Sequence gneisses, Langtang valley, Nepal, were chemically mapped and then dated in situ via Th–Pb ion‐microprobe analysis. Correlation of ages and chemistry reveals at least five different generations of monazite, ranging from c. 9 to >300 Ma. Petrological models of monazite chemistry provide a link between these generations and the thermal evolution of these rocks, yielding an age for the melting of Greater Himalayan rocks within the Main Central Thrust sheet (c. 16 Ma), and for the timing of thrust sheet emplacement that are younger than commonly viewed. Chemical characterization of monazite is vital prior to chronological microanalysis, and many ages previously reported for monazite from the Greater Himalayan Sequence are interpretationally ambiguous.     

CHIME dating of monazite, xenotime, zircon and polycrase: Protocol, pitfalls and chemical criterion of possibly discordant age data

This paper outlines the CHIME (chemical Th–U-total Pb isochron method) dating method, which is based on precise electron microprobe analyses of Th, U and Pb in Th- and U-bearing accessory minerals such as monazite, xenotime, zircon and polycrase. The age-mapping technique that is applicable to young monazite and zircon is also described. CHIME dating consists of analyzing multiple spots within homogeneous age domains that show sufficient compositional variation, and then these data are used to construct a “pseudo-isochron” from which an age can be obtained via regression. This method, when coupled with discrimination of possibly concordant age data by chemical criteria such as the (Ca + Si)/(Th + U + Pb + S) ratio for monazite and Ca and S contents for zircon, has the potential advantage of significant precision, and the ability to work with minerals that have a significant initial common Pb component. This technique can identify two or more homogeneous domains that are separated by age gaps smaller than the error on individual spot age analysis. Many features that are insignificant in major element analysis can have major impact in the acquisition of trace element data. Critical factors include the roles of collimator slit, detector gas, background estimation, accelerating voltage, probe current, X-ray interferences and count rate in affecting the accuracy, and a way to apply the Th and U interference correction without pure Th- and U-oxides or synthesized pure ThSiO₄. The age-mapping procedure for young monazite and zircon includes acquiring PbMα (or PbMβ) intensity of individual pixels with multiple spectrometers, correcting background with background maps computed from a measured background intensity by the intensity relationships determined in advance of the measurement, calibrating of intensity with standards and calculating of ages from the Th, U and Pb concentrations. This technique provides age maps that show differences in age domains on the order of 20 Ma with in monazite as young as 100 Ma. The effect of sample damage by irradiation of intense and prolonged probe measurement is also described.     

In situ U-Pb dating and element mapping of three generations of monazite: Unravelling cryptic tectonothermal events in low-grade terranes

In situ U-Pb dating of monazite and xenotime in sedimentary rocks from the mid-Archean Soanesville Group in the Pilbara Craton, yields ages for provenance, diagenesis and multiple low-grade metamorphic events. Detrital monazite and xenotime grains give dates >3250 Ma, whereas diagenetic xenotime provides a new minimum age of 3190 ± 10 Ma for deposition of the basal Soanesville Group, previously constrained between ∼3235 Ma and ∼2955 Ma. Metamorphic monazite provides evidence for three episodes of growth: at 2.88, 2.16 and 1.65 Ga. Element mapping of monazite for La, Sm, Y and Th reveals distinct cores and rims in some crystals that were used to guide the placement of analytical spots during in situ U-Pb dating by sensitive high-resolution ion microprobe (SHRIMP). Specifically, La and Sm distributions closely correlate with different generations of monazite. The presence of two generations in single monazite crystals highlights the need for characterizing mineral chemistry prior to geochronology. It also shows the importance of using in situ dating techniques rather than methods that rely on the analysis of entire, potentially multi-aged, crystals. The ages recorded by metamorphic monazite span more than one billion years and are interpreted to record cryptic tectonothermal events within the craton. The 2.88 Ga age coincides with a phase of regional deformation, metamorphism and gold mineralization along a major crustal lineament, whereas the most common monazite age population (at 2.16 Ga) corresponds with the migration of a foreland fold-and-thrust belt across the craton. The youngest age (1.65 Ga) coincides with an episode of tectonic reworking in the Capricorn Orogen along the southern Pilbara margin. The prolonged history of monazite growth may, in part, relate to channelized fluid flow during reactivation of long-lived N- to NE-trending crustal structures that transect the craton. Despite repeated episodes of metamorphism, the isotopic system in each generation of monazite remained unperturbed, yielding precise dates. The ability of monazite to record three separate events, and in some instances two events in a single crystal, distinguishes it from most other low-temperature mineral chronometers, which are readily reset during metamorphic overprinting. Low-temperature monazite geochronology can provide a detailed isotopic history of cryptic thermal events and reveal the temporal and spatial patterns of far-field fluid flow related to tectonic processes. The previously unrecognized history of crustal fluid flow in the Pilbara Craton has implications for chemical, mineralogical and isotopic studies seeking to understand conditions on the early Earth.     

Three generations of monazite in Austroalpine basement rocks to the south of the Tauern Window: evidence for Variscan, Permian and Eo-Alpine metamorphic events

Three monazite generations were observed in garnet-bearing micaschists from the Schobergruppe in the basement to the south of the Tauern Window, Eastern Alps. Low-Y monazite of Variscan age (321?±?14?Ma) and high-Y monazite of Permian age (261?±?18?Ma) are abundant in the mica-rich rock matrix and in the outer domains of large garnet crystals. Pre-Alpine monazite commonly occurs as polyphase grains with low-Y Variscan cores and high-Y Permian rims. Monazite of Eo-Alpine age (112?±?22?Ma) is rarer and was observed as small, partly Y-enriched grains (3?wt. %?Y₂O₃) in the rock matrix and within garnet. Based on monazite-xenotime thermometry, Y?+?HREE values in monazite indicate minimum crystallization conditions of 500?°C during the Variscan and 650?°C for the Permian and Alpine events, respectively. Garnet zoning and thermobarometric calculations with THERMOCALC 3.21 record an amphibolite facies, high-pressure stage of ~600?°C/13?C16?kbar, followed by a thermal maximum at 650?C700?°C and 6?C9?kbar. The Eo-Alpine age for these two events is supported by inclusions of Cretaceous monazite in the garnet domains used for thermobarometric constraints and through the high growth temperatures of Eo-Alpine monazite, which is consistent with that of the thermal maximum (~700?°C). The age and growth conditions of a few Mn-rich garnet cores, sporadically present within Eo-Alpine garnet, are unclear because inclusions of monazite, plagioclase and biotite necessary for thermobarometric- and age constraints are absent. However, based on monazite thermometry, Permian and Variscan metamorphic conditions were high enough for the growth of pre-Alpine garnet. The formation of Variscan garnet and its later resorption, plus Y-release, would also explain the high Y in Permian monazite, which cannot originate from preexisting Variscan monazite only. Monazite of Variscan, Permian and/or Eo-Alpine ages were also observed in other garnet-bearing micaschists from the Schobergruppe. This suggests that the basement of the Schobergruppe was overprinted by three discrete metamorphic events at conditions of at least lower amphibolite facies. While the Variscan event affected all parts of this basement, the younger events are more pronounced in its structurally lower units.     

Bulk chemical control on metamorphic monazite growth in pelitic schists and implications for U–Pb age data

Several petrographic studies have linked accessory monazite growth in pelitic schist to metamorphic reactions involving major rock‐forming minerals, but little attention has been paid to the control that bulk composition might have on these reactions. In this study we use chemographic projections and pseudosections to argue that discrepant monazite ages from the Mount Barren Group of the Albany–Fraser Orogen, Western Australia, reflect differing bulk compositions. A new Sensitive High‐mass Resolution Ion Microprobe (SHRIMP) U–Pb monazite age of 1027 ± 8 Ma for pelitic schist from the Mount Barren Group contrasts markedly with previously published SHRIMP U–Pb monazite and xenotime ages of c. 1200 Ma for the same area. All dated samples experienced identical metamorphic conditions, but preserve different mineral assemblages due to variable bulk composition. Monazite grains dated at c. 1200 Ma are from relatively magnesian rocks dominated by biotite, kyanite and/or staurolite, whilst c. 1027 Ma grains are from a ferroan rock dominated by garnet and staurolite. The latter monazite population is likely to have grown when staurolite was produced at the expense of garnet and chlorite, but this reaction was not intersected by more magnesian compositions, which are instead dominated by monazite that grew during an earlier, greenschist facies metamorphic event. These results imply that monazite ages from pelitic schist can vary depending on the bulk composition of the host rock. Samples containing both garnet and staurolite are the most likely to yield monazite ages that approximate the timing of peak metamorphism in amphibolite facies terranes. Samples too magnesian to ever grow garnet, or too iron‐rich to undergo garnet breakdown, are likely to yield older monazite, and the age difference can be significant in terranes with a polymetamorphic history.     

Monazite U-Pb dating of staurolite grade metamorphism in pelitic schists

A study of the occurrence of and relations between rare-earth element (REE) minerals in pelitic schists indicates that monazite forms at or near the P and T of the staurolite isograd. Samples at staurolite grade from the Silurian Perry Mountain Formation in the Rumford quadrangle of Maine yield monazite in sufficient quantities to permit accurate dating of the metamorphic events forming the monazites. The bulk chemistry of the metapelites, as seen in the major element abundances and REE patterns, does not vary significantly across the study area. Thus the appearance and disappearance of REE phases is assumed to reflect changes in metamorphic grade. In a sample from the biotite zone, scanning electron microscope and microprobe studies show allanite and monazite intimately associated on a 10 m scale. The texture suggest that metastable detrital monazite breaks down, distributing its REE components to allanite. From samples below staurolite grade in which monazite is not present, our observations suggest that REEs are partitioned into allanite. At or near the staurolite isograd monazite forms as a metamorphic mineral, initiating its role as a geochronometer. Garnet-biotite geothermometry on samples at this grade from this and other studies places constraints on the minimum temperature necessary to form monazite: 525° C±25°C at 3.1±0.25 kbar. A total of 15 separates from nine schist samples ranging up to sillimanite grade have been dated. Each date is remarkably concordant, even though petrologic and textural studies by previous workers have shown that the rocks in the area have been affected by at least three metamorphic episodes. Calculations indicate insignificant Th disequilibrium in these monazites. The conditions associated with the metamorphic events suggest that monazite remains closed to lead loss provided that subsequent metamorphisms are at or below sillimanite grade. Two distinct metamorphic events are resolved, one at around 400 Ma and one at about 370 Ma. The latter was due to thermal effects of a nearby pluton that yields concordant monazite ages of 363 Ma. This work suggests that in addition to dating plutonism and high-grade metamorphism, monazite should be viewed as a reliable geochronometer for moderate metamorphism of pelitic schists.     

In situ SHRIMP U-Pb dating of monazite integrated with petrology and textures: Does bulk composition control whether monazite forms in low-Ca pelitic rocks during amphibolite facies metamorphism?

Bulk composition and specific reaction history among common silicate minerals have been proposed as controls on monazite growth in metapelitic rocks during amphibolite facies metamorphism. It has also been implied that monazite that formed during greenschist facies metamorphism may be preserved unchanged under upper amphibolite facies conditions. If correct, this would make the interpretation of monazite ages in polymetamorphic rocks exceedingly difficult, because isotopic dates could vary significantly in rocks that have experienced identical metamorphic conditions but differ only slightly in whole-rock composition. Low-Ca pelitic schists from the Mount Barren Group in southwestern Australia display a range of whole-rock compositions in AFM space and different peak mineral assemblages resulting from amphibolite facies metamorphism (∼8 kb, 650 °C). In this study, we test whether bulk composition controls the formation of monazite through geochronology and textural evidence linking monazite growth with deformation and peak metamorphism. X-ray element mapping of monazite from the metapelitic rocks reveals concentric zoning in many grains with compositionally distinct cores and rims. In situ SHRIMP U-Pb geochronology of monazite yields two ²⁰⁷Pb/²⁰⁶Pb age populations. The cores, and texturally early monazite, give an age of 1209 ± 10 Ma, interpreted to record prograde metamorphism, whereas the rims and “late” monazite define a single population of 1186 ± 6 Ma, which is considered the likely age of peak thermal metamorphism. The growth of monazite was widespread in low-Ca pelitic schists representing a broad range of compositions in AFM space, indicating that variations in bulk composition in AFM space did not control the formation of monazite during amphibolite facies metamorphism in the Mount Barren Group.     

前寒武纪沉积岩中自生独居石的发现及其意义

由于受到葛家屯组中发现自生方铅矿的启发 ,首次于大连前寒武纪震旦系十三里台组泥岩中发现了自生独居石 ,这一发现为在中国北方前寒武纪沉积岩中寻找自生独居石提供了重要的线索。它为进一步探索 U、Th- Pb同位素测年拓展了新的研究领域和提供了可能性。本文列举了中国北方前寒武纪沉积岩中 Ce元素异常以及 REE较高的例证 ,认为上述地区都有可能发现自生独居石。同时介绍了最近又在北京十三陵中元古代的常州沟组和串岭沟组所发现自生独居石的新资料。研究表明 ,自生独居石的电子探针扫描形态 ,与岩浆岩、变质岩及砂矿中截然不同。在地质年代分布上 ,元古宙 REE相对丰度较高 ,特别是 L REE较高的泥质岩多数来自古陆壳上。资料对比结果显示 :在 L a+Ce+Nd、Yb+Y、Sm+Gd+Dy三角图中 ,北京十三陵元古宙泥质岩、大连震旦系十三里台组泥岩和辽南 -辽西中元古代泥质岩都属于近古陆的沉积类型。首次提出 ,中国北方元古宙沉积与南方震旦系磷块岩沉积环境存在明显的不同并反映在三角图中 ,前者离 L a+Ce+Nd端点近 ,而后者由于成因上属于洋流上升沉积物而远离该端点。按照大连震旦系十三里台组沉积环境特点 ,自生独居石应为生物成矿作用的产物 ,含矿物泥岩形成于总体氧化环境中的局部还原亚环境中。基于此 ,建立了