Granite-hosted mineral deposits of the New Ross area, South Mountain Batholith, Nova Scotia, Canada: P, T and X constraints of fluids using fluid inclusion thermometry and decrepitate analysis

Author(s):  
Sarah Carruzzo ◽  
Daniel J. Kontak ◽  
D. Barrie Clarke

The 370 Ma peraluminous South Mountain Batholith (SMB) intrudes Meguma Supergroup metasedimentary rocks in Nova Scotia. The New Ross area of the SMB contains polymetallic mineralisation (Sn, W, U, Mo, Cu and Mn) in pegmatite, greisen and vein directly or indirectly associated with highly evolved fractions of the SMB. Eight mineral deposits from this area have several fluid inclusion types hosted by quartz: (1) monophase liquid (L); (2) monophase vapour (V); (3) aqueous, L-V (4) aqueous, L-rich + solids; (5) aqueous, L-rich + halite. Inclusions have irregular to equant shapes and are pseudo-secondary or secondary. The irregularity and variability of L:V ratios within fluid inclusion populations suggest post-entrapment modifications of inclusions (i.e. necking).Thermometric data indicate three distinct fluids in terms of salinity: (1) 19-25 wt. % equiv. NaCl (rarely 14-25 wt. % NaCl equiv.), (2) 29-43 wt. % equiv. NaCl, and (3) 0-9 wt. % equiv. NaCl. Temperatures of first melting and ice/hydrohalife melting indicate CaCl2 in solution. Proximity of the deposits to Meguma Supergroup metasedimentary rocks suggests that this Ca component may be externally derived. The majority of the low-salinity fluid population has the composition of meteoric water. Electron microprobe analyses of artificially decrepitated mounds identify Na, Ca and K as major solutes, with a continuum in terms of compositions. Other solute components in the mounds are Fe and Ba, and a variety of metals of unknown speciation also occur (Cu, Zn, Fe, Ni). Homogenisation temperatures (Th) range from c. 80°C to 370°C, but for inclusion assemblages the range is 10°C to 20°C. Given the 3 kbar depth of emplacement of the SMB, estimated entrapment temperatures are c. 200°C to 550°C. The fluid inclusion data appear to reflect: (1) trapping of mixed Na-K-Ca brines during isobaric cooling in pegmatite and greisen deposits as indicated by large ranges in Th; (2) formation of deposits at different ambient pressures (i.e. depth); and (3) mixing of fluids of different reservoirs (i.e. magmatic, metamorphic, meteoric).

Geofluids ◽  
2017 ◽  
Vol 2017 ◽  
pp. 1-19 ◽  
Author(s):  
Qihai Shu ◽  
Yong Lai

The Haisugou porphyry Mo deposit is located in the northern Xilamulun district, northeastern China. Based on alteration and mineralization styles and crosscutting relationships, the hydrothermal evolution in Haisugou can be divided into three stages: an early potassic alteration stage with no significant metal deposition, a synmineralization sericite-chlorite alteration stage with extensive Mo precipitation, and a postmineralization stage characterized by barren quartz and minor calcite and fluorite. The coexistence of high-salinity brine inclusions with low-salinity inclusions both in potassic alteration stage (~440°C) and locally in the early time of mineralization stage (380–320°C) indicates the occurrence of fluid boiling. The positive correlations between the homogenization temperatures and the salinities of the fluids and the low oxygen isotopic compositions (δ18Ofluid < 3‰) of the syn- to postmineralization quartz together suggest the mixing of magmatic fluids with meteoric water, which dominated the whole mineralization process. The early boiling fluids were not responsible for ore precipitation, whereas the mixing with meteoric water, which resulted in temperature decrease and dilution that significantly reduced the metal solubility, should have played the major role in Mo mineralization. Combined fluid inclusion microthermometry and chlorite geothermometer results reveal that ore deposition mainly occurred between 350 and 290°C in Haisugou.


1980 ◽  
Vol 17 (1) ◽  
pp. 132-141 ◽  
Author(s):  
F. J. Longstaffe ◽  
T. E. Smith ◽  
K. Muehlenbachs

The oxygen isotope ratios for 127 rocks and coexisting minerals from Paleozoic granitoids and clastic metasedimentary rocks of southwestern Nova Scotia have been measured. The whole-rock δ18O values for samples of the South Mountain batholith range from 10.1–12.0‰.But discrete granitoid plutons, located to the south of the South Mountain batholith, have lower δ18O values (7.8–10.4‰). Coexisting minerals from the Nova Scotia granitoids are near isotopic equilibrium, indicating that the whole-rock δ18O values primarily reflect the δ18O of the magma, rather than secondary alteration processes. The Meguma Group clastic metasedimentary rocks that host the Nova Scotia granitoids range in δ18O from 10.1–12.9‰. These clastic metasedimentary rocks show no systematic geographic variation in δ18O. The greenschist facies Meguma Group rocks that host the South Mountain batholith have similar δ18O values to the amphibolite facies equivalents located about the southern discrete plutons. Large scale isotopic exchange between the Meguma Group and the South Mountain batholith, or the southern plutons, is not evident.The relatively high δ18O values of the peraluminous South Mountain batholith (10.1–12.0‰) indicate that it formed by anatexis of 18O-rich clastic metasedimentary rocks. The southern plutons were also derived by partial melting of clastic metasedimentary rocks, but their lower δ18O values reflect exchange of the source material with a low 18O reservoir (mafic magmas?) prior to, or during anatexis.The sheared Brenton pluton is much lower in δ18O (5.0‰) than any of the other rocks, probably because of exchange with low 18O fluids during shearing.


2004 ◽  
Vol 68 (1) ◽  
pp. 31-46 ◽  
Author(s):  
J. Zachariáš ◽  
J. Frýda ◽  
B. Paterová ◽  
M. Mihaljevič

AbstractThe major- and trace-element chemistry of pyrite and arsenopyrite from the mesothermal Roudný gold deposits was studied by electron microprobe and laser ablation ICP-MS techniques. In total, four generations of pyrite and two of arsenopyrite were distinguished. The pyrite is enriched in As through an Fe (AsxS1–x)2 substitution mechanism. The As-rich zones of pyrite-2 (up to 4.5 wt.% As) are also enriched in gold (up to 20 ppm), lead (commonly up to 220 ppm, exceptionally up to 1500 ppm) and antimony (commonly <600 ppm, rarely up to 1350 ppm). Positive correlation of As and Au in the studied pyrites is not coupled with an Fe deficiency, in contrast to Au-rich As-bearing pyrites in Carlintype gold deposits. The As-rich pyrite-2 coprecipitated with the Sb-rich (1 –4.2 wt.%) and Au-rich (40 –150 ppm) arsenopyrite-1. The younger arsenopyrite-2 is significantly less enriched in these elements (0 –70 ppm of Au).The chemical zonality of pyrites in the Roudný gold deposits reflects the chemical evolution of orebearing fluids that are not observed in any other mineral phases. The data available suggest relatively high activity of sulphur and low activities of arsenic and gold during crystallization of the older pyrite generation (pyrite-1). Later, after particular dissolution of pyrite-1, Au-rich As-bearing pyrite-2 and arsenopyrite precipitated. These facts suggest a marked increase in the arsenic and gold activities in ore-bearing fluids. The As-content of pyrite-2 decreases in an oscillatory manner from the core to the rim, reflecting changes in the As activity or/and in the P-T conditions. The As-bearing pyrites were formed at temperatures of at least 320–330°C, based on arsenopyrite thermometers and fluid inclusion data.


Clay Minerals ◽  
1984 ◽  
Vol 19 (4) ◽  
pp. 579-590 ◽  
Author(s):  
Tj. Peters ◽  
B. Hofmann

AbstractClay minerals of several hydrothermally altered zones in a 1200-m biotite-granite core from a drillhole in northern Switzerland were studied microscopically, by XRD and by electron microprobe. The minerals principally affected by the hydrothermal alteration were plagioclase (An5-An20) and, to a lesser extent, biotite. Illite, regularly interstratified illite-smectite and dioctahedral chlorite-smectite, dioctahedral chlorite, trioctahedral chlorite and kaolinite were detected in the alteration products. Commonly, two or more clay minerals occurred together in pseudomorphs after plagioclase. The mineral chemistry of the clay minerals showed a predominance of the substitution KAl for Si and, to a lesser extent, MgSi for Al. Fluid-inclusion data and the absence of pure smectite and epidote indicated temperatures of ∼200°C for the fluid that caused this alteration.


2017 ◽  
Vol 54 (7) ◽  
pp. 693-713 ◽  
Author(s):  
Michael A. MacDonald ◽  
D. Barrie Clarke

Melagranites (colour index > 20, with biotite > garnet > cordierite) constitute ∼0.1% of the area of the 7300 km2 peraluminous South Mountain Batholith (SMB), Nova Scotia. The melagranites occur as small bodies showing sharp to gradational contacts against the Meguma Supergroup country rocks, and coeval mingling contacts against other facies of the batholith. They also occur as elliptical or blocky metre-scale enclaves elsewhere in the SMB. Characteristic petrological features of the melagranites include high modal abundances of sulphide minerals, strongly reacted metasedimentary xenoliths, mafic mineral-rich clots, apparent porphyritic textures with highly variable proportions of alkali feldspar megacrysts, and allotriomorphic-granular textures. Chemically and isotopically, melagranite rocks have wide compositional variations. In most major-element, trace-element, and isotopic variation diagrams, the melagranites lie on mixing lines between the more abundant granodioritic and monzogranitic phases of the SMB and the metasedimentary rocks of the Meguma Supergroup. Textural evidence, supported by published experimental evidence, suggests that the garnet, cordierite, and K-feldspar are peritectic phases resulting from incongruent melting of the pelitic fraction of the Meguma metasedimentary country rocks. The field relations, mineral assemblages, textural features, and chemical compositions of the melagranites all point to the melagranites as highly concentrated contamination zones in the SMB, representing small portions of the batholith that have failed either to complete the assimilation process or to disperse their contaminants widely in the batholith. As such, these rarely preserved melagranites provide petrogenetic information disproportionate in importance to their abundance in the batholith, especially about the significant role of contamination and assimilation in determining the physical and chemical composition of the SMB. Without preservation of melagranites in the SMB, and by extension all granite bodies, the petrogenetic importance of contamination is difficult to assess, even with trace-element and isotopic data. The present study shows that high quality field observations are as important in deciphering petrogenesis as chemical data.


2001 ◽  
Vol 38 (9) ◽  
pp. 1285-1299 ◽  
Author(s):  
Nicholas Culshaw ◽  
Pradeep Bhatnagar

In southern Nova Scotia, the Devonian South Mountain Batholith was emplaced into metasedimentary rocks of the Cambro-Ordovician Meguma Group at ca. 370 Ma. The contact of the eastern end of the South Mountain Batholith transects at a high angle the trace of subhorizontal, upright Acadian (mid-late Devonian) folds formed in the Meguma Group. At two locations, where the contact is well exposed, there are contrasting structures in the country rocks adjacent to Acadian anticlinoria and synclinoria, respectively. Regional folds are affected by ductile deformation where anticlinoria abut the batholith but are undisturbed at the synclinoria. At the anticlinorial contacts, the metasedimentary bedding youngs towards the granite, and granite side-down shear resulted in a belt in which bedding is transposed to a new contact-parallel fabric. Deflection of linear structures that were initially horizontal in the Acadian folds (e.g., intersection lineations) illustrates the granite side-down shear. The reorientation of initially horizontal linear structures gradually diminishes as the contact is followed from the anticlinoria to the synclinoria, where the regional fold geometry is preserved right up to the contact, showing that there is no granite side-down shear in the synclinoria at the present level of erosion. Two models that potentially explain this variation in contact structure are discussed. In the first, it is explained as an artifact of emplacement of the batholith late in the growth of the Acadian folds, in which the horizontal, upright anticlinoria amplified and moved upward relative to the pluton. A shear zone was formed parallel to the contact along the thermally softened tip of the anticlinoria. The synclinoria remained fixed vertically and there was no differential movement between granite and country rock. Thus, regional structures and evidence for stoping are most widely preserved in the synclinoria, where they were not overprinted by the marginal shearing. The second model invokes floor-down emplacement of magma into folds of layered sediments with contrasting mechanical properties. The erosion surface within the synclinoria intersects slates of the Halifax Formation with mechanical properties that favour emplacement predominantly by dyking and stoping. Below the level of erosion, the stratigraphically underlying Goldenville Formation, having different mechanical properties than the Halifax, presumably is displaced downwards predominantly by ductile deformation (pure and simple shear). Within the anticlinoria, where the Goldenville Formation is exposed, the requirement of a level pluton floor necessitates that downward deflection is accompanied by relatively high ductile strains in the wall rock. A third possible model that combines features of the syntectonic and floor-down models is an obvious option.


1996 ◽  
Vol 60 (403) ◽  
pp. 927-936 ◽  
Author(s):  
Meideno Que ◽  
Alistair R. Allen

AbstractSericitization in three separate pulses of the Rosses Granite Ring Complex, Co. Donegal, Ireland, has been investigated texturally and chemically using electron microscopy, electron microprobe and fluid inclusion thermometry. The sericitization, which is restricted to the cores of plagioclase, is associated with pores which are abundant in the cores, but absent in the margins. Alkali feldspar, although porous, is unaltered. Associated with the sericitization is alteration of the adjacent primary plagioclase within the cores of grains to a more sodic composition.It is postulated that the sericitization resulted from the action of externally derived secondary hydrothermal fluids, which gained access to the pores in the plagioclase via now sealed microfractures, formed either by contraction during cooling of the Rosses Complex, or more likely by hydraulic fracturing by the fluids themselves. Limited fluid/rock ratios restricted the degree of sericitization within the host plagioclase, whilst an absence of alteration in alkali feldspar may have been due to the inaccessibility of pores in the alkali feldspar to the hydrothermal fluids at the time of alteration. Fluid inclusion data suggest that the fluids were of low salinity, and that the sericitization took place at an early stage in the cooling history of the Rosses Complex at temperatures between 400 and 600°C. It is further contended that greisenization in the Rosses Complex predated the sericitization and that the greisenization may have been due solely to volatile-rich late-stage magmatic fluids.


Minerals ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 64 ◽  
Author(s):  
Nurullah Hanilçi ◽  
Gülcan Bozkaya ◽  
David A. Banks ◽  
Ömer Bozkaya ◽  
Vsevolod Prokofiev ◽  
...  

The deposit occurs in a mid-Miocene monzonite magmatic complex represented by three different intrusions, namely Intrusion 1 (INT#1), Intrusion 2 (INT#2, INT #2A), and Intrusion 3 (INT#3). Gold mineralization is hosted in all intrusions, but INT#1 is the best mineralized body followed by INT#2. SEM-CL imaging has identified two different veins (V1 and V2) and four distinct generations of quartz formation in the different intrusions. These are: (i) CL-light gray, mosaic-equigranular quartz (Q1), (ii) CL-gray or CL-bright quartz (Q2) that dissolved and was overgrown on Q1, (iii) CL-dark and CL-gray growth zoned quartz (Q3), and (iv) CL-dark or CL-gray micro-fracture quartz fillings (Q4). Fluid inclusion studies show that the gold-hosted early phase Q1 quartz of V1 and V2 veins in INT#1 and INT#2 was precipitated at high temperatures (between 424 and 594 °C). The coexisting and similar ranges of Th values of vapor-rich (low salinity, from 1% to 7% NaCl equiv.) and halite-bearing (high salinity: >30% NaCl) fluid inclusions in Q1 indicates that the magmatic fluid had separated into vapor and high salinity liquid along the appropriate isotherm. Fluid inclusions in Q2 quartz in INT#1 and INT#2 were trapped at lower temperatures between 303 and 380 °C and had lower salinities between 3% and 20% NaCl equiv. The zoned Q3 quartz accompanied by pyrite in V2 veins of both INT#2 and INT#3 precipitated at temperatures between 310 and 373 °C with a salinity range from 5.4% to 10% NaCl eq. The latest generation of fracture filling Q4 quartz, cuts the earlier generations with fluid inclusion Th temperature range from 257 to 333 °C and salinity range from 3% to 12.5% NaCl equiv. The low salinity and low formation temperature of Q4 may be due to the mixing of meteoric water with the hydrothermal system, or late-stage epithermal overprinting. The separation of the magmatic fluid into vapor and aqueous saline pairs in the Q1 quartz of the V1 vein of the INT#1 and INT#2 and CO2-poor fluids indicates the shallow formation of the Kışladağ porphyry gold deposit.


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