Metamorphism and gold mineralization in the Blue Ridge, southernmost Appalachians
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Lode gold mineralization in the Blue Ridge of the southernmost Appalachians is hosted by metavolcanic rocks (e.g., Anna Howe mine, AL; Royal Vindicator mine, GA), metaplutonic rocks (e.g., Hog Mountain mine, AL), and metasedimentary rocks (e.g., Lowe, Tallapoosa, and Jones Vein mines, AL). Most gold occurs in synkinematic quartz + or - plagioclase + or - pyrite + or - pyrrhotite + or - chlorite veins localized along polydeformational faults that juxtapose rocks with significantly different peak metamorphic mineral assemblages.Mineralogy, chemistry, and O and H isotope studies suggest that the three types of host rocks have undergone differing amounts and types of alteration during mineralization. Limited wall-rock alteration in metavolcanic- and metasediment-hosted deposits, and relatively extensive wall-rock alteration in granitoid-hosted deposits, suggests that most deposits formed from fluids that were close to equilibrium with metavolcanic and metasedimentary rocks. Stable isotope compositions of the fluids calculated from vein minerals and vein selvages are consistent with a predominantly metasedimentary fluid source, but vary from deposit to deposit (-22 to -47ppm delta D, 4-5ppm, delta 18 O, and 5-7ppm delta 34 S at Anna Howe and Royal Vindicator; -48 to -50ppm delta D, 9-13ppm delta 18 O, and ca. 19ppm delta 34 S at Lowe and Jones Vein; and -22 to -23ppm delta D, 8-11ppm delta 18 O, 9-10ppm delta 34 S, and -6 delta 13 C at Hog Mountain). Silicate mineral thermobarometry of vein, vein selvage, and wall-rock mineral assemblages indicate that mineralization and regional metamorphism occured at greenschist to amphibolite facies (480 degrees + or - 75 degrees C at Anna Howe, 535 degrees + or - 50 degrees C at 6.4 + or - 1 kbars at Lowe, 530 degrees + or - 50 degrees C at 6.9 + or - 1 kbars at Tallapoosa, and 460 degrees + or - 50 degrees C at 5.5 + or - 1 kbars at Hog Mountain). Oxygen isotope fractionation between vein minerals and selvage minerals consistently records equilibration temperatures that are similar to or slightly lower than those estimated from silicate thermometry.Auriferous veins contain numerous fluid inclusions that were emplaced in several stages and can be subdivided into five compositional types based on salt and CO 2 concentrations. Fluid inclusion isochores for early formed inclusions from these veins intercept the pressure and temperature conditions estimated from silicate mineral thermobarometry and stable isotope thermometry, and are compatible with entrapment at those conditions. These fluids exhibit significant variation in salinity (X (sub NaCl equiv ) ) = 0.0-0.2) and CO 2 (X (sub CO 2 ) = 0.0-0.2), suggesting variation in fluid-wall-rock interaction that accompanied gold deposition during declining temperatures. Less abundant and later fluids within the veins are dominantly CO 2 .The association of gold mineralization with structurally controlled concordant and discordant quartz sulfide veins, and the temperatures and pressures of wall-rock alteration and regional metamorphism indicate that the present distribution of gold is a result of metamorphism during progressive D 2 -D 3 deformation. Isotopic data for alteration envelopes date this event as Alleghanian: 279 + or - 14 Ma (K-Ar whole rock) and 343 + or - 18 Ma (K-Ar biotite) at Lowe; and 315 + or - 18 Ma (Rb-Sr whole-rock isochron; 87 Sr/ 86 Sr i = 0.7061 + or - 0.0008) and 294 + or - 16 Ma (K-Ar whole-rock) at Hog Mountain. Available data are compatible with development of the lodes during early Alleghanian overthrusting of allochthons over sedimentary rocks of the autochthonous North American margin. The implication is that the fluids were derived from metasedimentary and/or metavolcanic formations in the lower parts of the crystalline thrust stack (or possibly from underlying autochthonous sedimentary formations), ascended along permeable fault zones, and were emplaced as veins into dilatent areas in and adjacent to the fault zones.Keywords:
Greenschist
Wall rock
Lode
<p>Deformation of natural mafic rocks by viscous deformation mechanisms can occur even at low temperature conditions. In such instances, crystal plastic mechanisms are not operative, as their activity is restricted to very high temperatures for amphiboles, pyroxenes, and plagioclase. Instead, simultaneous mineral reactions may facilitate deformation at low temperature conditions. The gabbro from the Lyngen Magmatic Complex (LMC) constitutes a good example of such processes, because it has experienced deformation at low temperatures of greenschist to lower amphibolite-facies conditions, and the rock has been transformed from gabbro to greenschist. This study focuses on detailed analysis of deformation processes, metamorphic reactions and fabric development in the LMC gabbro. Most samples are overprinted by epidote amphibolite and greenschist-facies mineral assemblages. Preliminary observations distinguish two different types of amphiboles, which have been interpreted as different generations. The predominant type defines the stretching lineation and shows long prismatic habits whereas the less abundant type crystallized in a sub- to anhedral manner. The metamorphic conditions of growth for each amphibole type is yet not well constrained. However, we initially interpret the former to grow during epidote amphibolite- or greenschist facies-conditions, whereas the latter could represent relict grains from the original magmatic assemblage or products generated at amphibolite- or epidote amphibolite-facies conditions. Further analysis will determine the orientation, geochemistry and metamorphic conditions during growth for both amphibole types. A recent model proposed for eclogites suggests that simultaneous mineral growth and deformation can result in new products growing in a preferred direction. Such preferential growth can generate a shape preferred orientation parallel to the lineation, which results in the formation of crystal preferred orientations (CPO). We aim to test if similar microstructural observations can be translated to the amphiboles of the LMC gabbro. In such case, amphibole CPO&#8217;s would not be the product of crystal plasticity but of preferential growth. The large scale deformation of the LMC emphasizes the relevance of these results, as it would demonstrate that the interaction between mineral reactions and deformation can play a major role on regional deformation of large mafic bodies, such as the ocean floor.</p>
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Two textures of optically negative chlorite and one of positive chlorite can be distinguished in low-grade metavolcanic rocks of the St. Anthony Complex, Newfoundland. The negative chlorite is a low-temperature polytype. Recrystallization from negative to positive chlorite was induced by deformation during and after lower-greenschist-facies metamorphism. Interlayered and intermixed positive and negative chlorites in the matrix of undeformed metavolcanic rocks of the Dunn Point Formation, Nova Scotia, are cross-cut by veins of positive chlorite. Negative chlorite has recrystallized to positive chlorite owing to rising metamorphic temperature under conditions of the prehnite-pumpellyite facies. The negative chlorite is more magnesian than the analogous chlorite in the Newfoundland rocks, and it has recrystallized to the positive form at a lower temperature.--Modified journal abstract.
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For rock-forming minerals, the extent and the behavior of solid solution are understandable only if considered in ttre context of a rigorous petrological framework, as has been shown repeatedly in the met?morphic perology literature. Herein, we present a study of the composition of trioctahedral chlorites, with special focus on nen-limigillg minsl4l 455e6!lages in rocks of low metamorphic grade. The goal has been to discern and understand any systematic changes of chlorite composition due to changing T' P' and bulk-rock composition. The three main compositional variations shown by the metamorphic chlorite in this study include the ratio Fe/Mg, the extent ofTschermak substitution, and deviation from trioctahedral toward dioctahedral chlorite. Our database includes 2619 chlorite compositions, of which 450 are selected from literature covering the temperature range subgreenschist - amphibolite facies, and,2169 are newly determined compositions from greenschist-facies rocks. All samples used are classified according to metemorphic grade, pressure, and brtk-rock composition, thereby establishing groups and subgroups of analytical data. These data are plotted on diagrams aimed at enabling one to discern more specifically how bulk-rock composition, temperatue and pressure affect the three main compositional variations of chlorite from typical meramorphic rocks. Each of ttrese parameters controls chlorite composition to some extent, but the control by the bulk-rock chemistry is clearly dominant. Comm661y it largely obscures the systematic compositional changes caused by temperatue and pressure. Thus, despite numerous attempts, it is evident that chlorite composition by itself is non-viable for geothermobarometric purposes in the case of the non-lirniting assemblages tlpical of the greenschist facies. Attempts to use chlorite from such assemblages for geothermobarometry should be restricted solely to approaches involving cation exchange with some coexisting phase(s).
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A subcircular area of about 650 km 2 in northern California and southwestern Oregon is occupied by rocks of the greenschist metamorphic facies called the Condrey Mountain Schist. This greenschist terrane is bordered on the east and west by rocks belonging to the amphibolite metamorphic facies that structurally overlie and are thrust over the Condrey Mountain Schist. The amphibolite facies is succeeded upward by metavolcanic and metasedimentary rocks belonging to the greenschist metamorphic facies. The Condrey Mountain Schist is composed predominantly of quartz-muscovite schist and lesser amounts of actinolite-chlorite schist formed by the metamorphism of graywacke and spilitic volcanic rocks that may have belonged to the Galice Formation of Late Jurassic age. Potassium-argon age determinations of 141?4 m.y. and 155?5 m.y. obtained on these metamorphic rocks seem to be incompatible with the Late Jurassic age usually assigned the Galice. The rocks that border the amphibolite facies are part of an extensive terrane of metavolcanic and metasedimentary rocks belonging to the western Paleozoic and Triassic belt. The metavolcanic rocks include some unmetamorphosed spilite but are mostly of the greenschist metamorphic facies composed of oligoclase (An15-20) and actinolite with subordinate amounts of chlorite and clinozoisiteepidote. The interbedded sedimentary rocks are predominantly argillite and slaty argillite, less commonly siliceous argillite and chert, and a few lenticular beds of marble. On the south, high-angle faults and a tabular granitic pluton separate the greenschist metavolcanic terrane from the amphibolite facies rocks; on the east, nonfoliated amphibolite is succeeded upward, apparently conformably, by metasedimentary rocks belonging to the greenschist metavolcanic terrane. In the southern part of Condrey Mountain quadrangle, an outlier of a thrust plate composed of the Stuart Fork Formation overlies the metavolcanic and metasedimentary rocks. The Stuart Fork in this region is composed of siliceous phyllite and phyllitic quartzite and is believed to be the metamorphosed equivalent of rocks over which it is thrust. In the Yreka-Fort Jones area, potassium-argon determinations on mica from the blueschist facies in the Stuart Fork gave ages of approximately 220 m.y. (Late Triassic) for the age of metamorphism. Rocks of the amphibolite facies structurally overlie the Condrey Mountain Schist along a moderate to steeply dipping thrust fault. The amphibolite terrane is composed of amphibolite and metasedimentary rocks in approximately equal amounts accompanied by many bodies of serpentinite and a number of gabbro and dioritic plutons. Most of the amphibolite is foliated, but some is nonfoliated; the nonfoliated amphibolite has an amphibolite mineralogy and commonly a relict volcanic rock texture. The nonfoliated amphibolite occurs on the southern and eastern borders of the amphibolite terrane between the areas offoliated amphibolite and the overly ing metavolcanic and metasedimentary rocks. Hornblende and plagioclase (An30-35) are the characteristic minerals, indicating that the rocks are of the almandine-amphibolite metamorphic facies. The metasedimentary rocks interbedded with the amphibolites include siliceous schist and phyllite, minor quartzite, and subordinate amounts of marble. Potassium-argon age dates obtained on hornblende from foliated amphibolite yield ages of 146?4 and 148? 4 m.y., suggesting a Late Jurassic metamorphic episode. Mafic and ultramafic rocks are widespread in the amphibolite terrane but are almost entirely absent from the area of greenschist facies metavolcanic and metasedimentary rocks. The ultramafic rocks, predominantly serpentinite, occur as a few large bodies and many small tabular concordant bodies interleaved with the foliated rocks. The ultramafic rocks include harzburgite and d1lIlite and their serpentinized equivalents. In the Condrey Mountain quadrangle, probably more t
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Abstract The production of large volumes of fluid from metabasic rocks, particularly in greenstone terranes heated across the greenschist–amphibolite facies transition, is widely accepted yet poorly characterized. The presence of carbonate minerals in such rocks, commonly as a consequence of sea‐floor alteration, has a strong influence, via fluid‐rock buffering, on the mineral equilibria evolution and fluid composition. Mineral equilibria modelling of metabasic rocks in the system Na 2 O‐CaO‐FeO‐MgO‐Al 2 O 3 ‐SiO 2 ‐CO 2 ‐H 2 O (NCaFMASCH) is used to constrain the stability of common metabasic assemblages. Calculated buffering paths on T – X CO2 pseudosections, illustrate the evolution of greenstone terranes during heating across the greenschist‐amphibolite transition. The calculated paths constrain the volume and the composition of fluid produced by devolatilization and buffering. The calculated amount and composition of fluid produced are shown to vary depending on P – T conditions, the proportion of carbonate minerals and the X CO2 of the rocks prior to prograde metamorphism. In rocks with an initially low proportion of carbonate minerals, the greenschist to amphibolite facies transition is the primary period of fluid production, producing fluid with a low X CO2 . Rocks with greater initial proportions of carbonate minerals experience a second fluid production event at temperatures above the greenschist to amphibolite facies transition, producing a more CO 2 ‐rich fluid ( X CO2 = 0.2–0.3). Rocks may achieve these higher proportions of carbonate minerals either via more extensive seafloor alteration or via infiltration of fluids. Fluid produced via devolatilization of rocks at deeper crustal levels may infiltrate and react with overlying lower temperature rocks, resulting in external buffering of those rocks to higher X CO2 and proportions of carbonate minerals. Subsequent heating and devolatilization of these overlying rocks results in buffering paths that produce large proportions of fluid at X CO2 = 0.2–0.3. The production of fluid of this composition is of importance to models of gold transport in Archean greenstone gold deposits occurring within extensive fluid alteration haloes, as these haloes represent the influx of fluid of X CO2 = 0.2–0.3 into the upper crust.
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