The sulfur content of Archean volcanic rocks and a comparison with ocean floor basalts

1978 ◽  
Vol 15 (5) ◽  
pp. 715-728 ◽  
Author(s):  
A. J. Naldrett ◽  
A. M. Goodwin ◽  
T. L. Fisher ◽  
R. H. Ridler

In this paper we report the sulfur contents of 1056 basalts, andesites, dacites and rhyolites of known major element composition from the Rankin–Ennadai, Birch Lake – Uchi Lake, Lake of the Woods – Wabigoon Lake, Timmins and Skead Archean greenstone belts of the Canadian Shield. The sulfur contents of 299 ocean floor basalts and 68 sub-aerial or shallow water extrusive rocks are also reported. Sulfur contents for rocks of a given class are highly variable, ranging from near zero to several thousand parts per million (ppm). However, when averages for each of the rock classes are examined, the data from the two best documented of the Archean greenstone belts exhibit the same positive correlation between sulfur and total Fe content of the rocks. The trend for the Rankin–Ennadai belt coincides almost exactly with that reported earlier for the Blake River Group, approximating that expected if the rocks were saturated in sulfide at the time of extrusion. Rocks from the Lake of the Woods – Wabigoon Lake, Timmins and Skead areas seem to be somewhat poorer in sulfur than those from the Rankin–Ennadai and Blake River belts.Despite the fact that all evidence in the literature for fresh glassy pillow rims indicates that modern ocean floor basalts are saturated in sulfide, our average values for these ocean floor rocks are much lower than the predicted saturation levels, suggesting that the rocks have lost one-half to three-fourths of their sulfur, presumably through reaction with sea water. It is suggested that the reason for the Archean basalts retaining most of their sulfur despite the extensive redistribution that has occurred, whereas modern ocean floor basalts lose so much, may be due to the Archean rocks accumulating much more quickly and being exposed to direct interaction with sea water for a much shorter time than the modern rocks.

1980 ◽  
Vol 17 (5) ◽  
pp. 560-568 ◽  
Author(s):  
G. S. Clark ◽  
S.-P. Cheung

Rb–Sr whole-rock ages have been determined for rocks from the Oxford Lake – Knee Lake – Gods Lake greenstone belt, in the Superior Province of northeastern Manitoba.The age of the Magill Lake Pluton is 2455 ± 35 Ma (λ87Rb = 1.42 × 10−11 yr−1), with an initial 87Sr/86Sr ratio of 0.7078 ± 0.0043. This granitic stock intrudes the Oxford Lake Group, so it is post-tectonic and probably related to the second, weaker stage of metamorphism.The age of the Bayly Lake Pluton is 2424 ± 74 Ma, with an initial 87Sr/86Sr ratio of 0.7029 ± 0.0001. This granodioritic batholith complex does not intrude the Oxford Lake Group. It is syn-tectonic and metamorphosed.The age of volcanic rocks of the Hayes River Group, from Goose Lake (30 km south of Gods Lake Narrows), is 2680 ± 125 Ma, with an initial 87Sr/86Sr ratio of 0.7014 ± 0.0009.The age for the Magill Lake and Bayly Lake Plutons can be interpreted as the minimum ages of granitic intrusion in the area.The age for the Hayes River Group volcanic rocks is consistent with Rb–Sr ages of volcanic rocks from other Archean greenstone belts within the northwestern Superior Province.


Recent work has determined the depth of the Mohorovičić discontinuity at sea and has made it likely that peridotite xenoliths in basaltic volcanic rocks are samples of material from below the discontinuity. It is now possible to produce a hypothetical section showing the transition from a continent to an ocean. This section is consistent with both the seismic and gravity results. The possible reactions of the crust to changes in the total volume of sea water are dis­cussed. It seems possible that the oceans were shallower and the crust thinner in the Archean than they are now. If this were so, some features of the oldest rocks of Canada and Southern Rhodesia could be explained. Three processes are described that might lead to the formation of oceanic ridges; one of these involves tension, one compression and the other quiet tectonic conditions. It is likely that not all ridges are formed in the same way. It is possible that serpentization of olivine by water rising from the interior of the earth plays an important part in producing changes of level in the ocean floor and anomalies in heat flow. Finally, a method of reducing gravity observations at sea is discussed.


Minerals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 242 ◽  
Author(s):  
Lucie Mathieu ◽  
Alexandre Crépon ◽  
Daniel J. Kontak

In Archean greenstone belts, magmatism is dominated by intrusive and volcanic rocks with tholeiitic affinities, as well as tonalite- and granodiorite-dominated large-volume batholiths, i.e., tonalite–trondhjemite–granodiorite (TTG) suites. These intrusions are associated with poorly documented mineralization (Cu-Au porphyries) that, in the Neoarchean Abitibi Subprovince (>2.79 to ~2.65 Ga), Superior Province, Canada, are associated with diorite bearing plutons, i.e., tonalite–trondhjemite–diorite (TTD) suites. The importance of TTG versus TTD suites in the evolution of greenstone belts and of their magmatic-hydrothermal systems and related mineralization is unconstrained. The aim of this study was to portray the chemistry and distribution of these suites in the Abitibi Subprovince. The study used data compiled by the geological surveys of Québec and Ontario to evaluate the chemistry of TTG and TTD suites and uncovered two coeval magmas that significantly differentiated (fractional crystallization mostly): 1) a heavy rare earth elements (HREE)-depleted tonalitic magma from high pressure melting of an hydrated basalt source; and 2) a hybrid HREE-undepleted magma that may be a mixture of mantle-derived (tholeiite) and tonalitic melts. The HREE-depleted rocks (mostly tonalite and granodiorite) display chemical characteristics of TTG suites (HREE, Ti, Nb, Ta, Y, and Sr depletion, lack of mafic unit, Na-rich), while the other rocks (tonalite and diorite) formed TTD suites. Tonalite-dominated magmatism, in the Abitibi Subprovince, comprises crustal melts as well as a significant proportion of mantle-derived magmas and this may be essential for Cu-Au magmatic-hydrothermal mineralizing systems.


Variations in trace element contents and inter-element ratios of deep-sea basalts are much more marked than variations in major element contents. This paper explores possible reasons for the variations which have been discovered. Inadequacy of sampling techniques may be responsible for some reported differences, but variations due to this cause are unlikely to approach the magnitude of reported variations. Some variation in samples from restricted areas of the ocean floor can be correlated with variation in the degree of silica saturation of the basalts. Submarine alteration of lavas by reaction with sea water is another possible cause of variation. Studies of metamorphosed deep-sea basalts suggest that very low-grade metamorphism may cause some, though slight, elemental migration. Studies on ultrabasic rocks show variations in trace element contents which, to some degree, appear to complement the variations encountered in basalts, suggesting that the extent of partial melting in the mantle during basaltic genesis influences the trace element contents of the products of melting. However, when such possible explanations have been considered, there remain variations in trace element contents of otherwise comparable basalts from different parts of the ocean floor, which appear to represent real variations in the trace element contents of the erupted basaltic magmas. In view of the difficulty of explaining such differences by contamination of magmas on their way to the surface, it is suggested that variations exist in the trace element contents of mantle material at the levels of basaltic genesis. Geochemical provinces exist in oceanic areas just as they do in continental regions.


2003 ◽  
Vol 40 (3) ◽  
pp. 431-445 ◽  
Author(s):  
Charles Maurice ◽  
Don Francis ◽  
Louis Madore

Numerous small remnants of Archean greenstone belts in the Northern Superior Province (ca. 2875–2710 Ma) have chemical characteristics similar to those of the larger greenstone belts of the Southern Superior Province, and preserve direct evidence of crustal conditions prior to the major volcanic events of the late Archean (Wawa–Abitibi subprovinces; ca. 2760–2700 Ma). Three of the best preserved belts are engulfed in tonalite intrusions of the Faribault-Thury Complex (FTC) and exhibit common chemical characteristics, which may imply a similar origin. The dominant tholeiitic basalts typically have MgO contents > 7 wt.%, TiO2 < 1 wt.% and nearly flat rare-earth element (REE) patterns (La/Smn = 0.77–1.22; Gd/Ybn = 0.86–1.20). Associated komatiites have flat to depleted REE patterns (La/Smn = 0.45–0.95), high Al2O3/TiO2 (>15), low CaO/Al2O3 (<1.2), and chondritic Gd/Yb ratios similar to 2.7 Ga Al-undepleted komatiites. The trace-element ratios of komatiitic rocks are indistinguishable from those of the associated tholeiites, suggesting either a derivation from similar mantle sources or a comagmatic relationship (Nb/Thpm = 0.8–1.1; La/Cepm = 0.9–1.3; Nb/Ce = 0.7–0.9; Y/Hopm ~1; and Th/Lapm = 0.7–1.1). Numerical modelling of trace and major elements during low-pressure crystal fractionation reproduces the spectrum of both inferred liquid and cumulate compositions and is consistent with a comagmatic origin between the komatiites and tholeiites. The relatively low Nb/Th ratios of these mid-Archean volcanic rocks relative to both modern day basalts and late Archean basalts may indicate that they were derived from a mantle source that had not lost its crustal components, nor seen significant recycled oceanic crust (high Nb/Th). The extraction of continental crust from this Archean mantle source might then postdate the FTC volcanism, and may be associated with the generation of the voluminous tonalites that engulf the belts.


1989 ◽  
Vol 53 (4) ◽  
pp. 859-871 ◽  
Author(s):  
Ján Veizer ◽  
Jochen Hoefs ◽  
D.R. Lowe ◽  
P.C. Thurston

The Holocene ◽  
2011 ◽  
Vol 21 (7) ◽  
pp. 1037-1048 ◽  
Author(s):  
Bergrún Arna Óladóttir ◽  
Olgeir Sigmarsson ◽  
Gudrún Larsen ◽  
Jean-Luc Devidal

The Holocene eruption history of subglacial volcanoes in Iceland is largely recorded by their tephra deposits. The numerous basaltic tephra offer the possibility to make the tephrochronology in the North Atlantic area more detailed and, therefore, more useful as a tool not only in volcanology but also in environmental and archaeological studies. The source of a tephra is established by mapping its distribution or inferred via compositional fingerprinting, mainly based on major-element analyses. In order to improve the provenance determinations for basaltic tephra produced at Grímsvötn, Bárdarbunga and Kverkfjöll volcanic systems in Iceland, 921 samples from soil profiles around the Vatnajökull ice-cap were analysed for major-element concentrations by electron probe microanalysis. These samples are shown to represent 747 primary tephra units. The tephra erupted within each of these volcanic system has similar chemical characteristics. The major-element results fall into three distinctive compositional groups, all of which show regular decrease of MgO with increasing K2O concentrations. The new analyses presented here considerably improve the compositional distinction between products of the three volcanic systems. Nevertheless, slight overlap of the compositional groups for each system still remains. In situ trace-element analyses by laser-ablation-inductively-coupled-plasma-mass-spectrometry were applied for better provenance identification for those tephra having similar major-element composition. Three trace-element ratios, Rb/Y, La/Yb and Sr/Th, proved particularly useful. Significantly higher La/Yb distinguishes the Grímsvötn basalts from those of Bárdarbunga and Rb/Y values differentiate the basalts of Grímsvötn and Kverkfjöll. Additionally, the products of Bárdarbunga, Grímsvötn and Kverkfjöll form distinct compositional fields on a Sr/Th versus Th plot. Taken together, the combined use of major- and trace-element analyses in delineating the provenance of basaltic tephra having similar major-element composition significantly improves the Holocene tephra record as well as the potential for correlations with tephra from outside Iceland.


1978 ◽  
Vol 42 (322) ◽  
pp. 209-220 ◽  
Author(s):  
Stefán Arnórsson

SummaryHigh-temperature geothermal fields in Iceland represent localized anomalies of hot, altered rock in the uppermost part of the crust, which coincide with points of maximum tectonic/magmatic activity. These points correspond to the intersection of oblique fault swarms to the plate boundaries. Geothermal activity under mid-ocean ridges follows probably similar tectonic/magmatic anomalies.Due to high permeability sea-water invades the bed-rock of the Reykjanes Peninsula, Iceland, and is overlain by a variably thick lens of dilute ground water of meteoric origin. The variable degree of salinity of geothermal waters in the Reykjanes Peninsula has resulted from different degree of mixing of fresh ground water with the underlying sea-water-ground-water in the downflow zones around the geothermal fields. At Reykjanes the geothermal water represents heated sea-water without any freshwater mixing. The difference in the composition of sea-water or sea-water/fresh water mixtures and the geothermal waters is due to basalt/water interaction at elevated temperatures. The major-element chemistry of the geothermal water represents an equilibrium composition at the relevant aquifer temperatures. The activities of silica, calcium, sulphate, and carbonate are thus limited by the solubilities of quartz, anhydrite, and calcite. Fluoride activity is thought to be controlled by an ionic exchange reaction where it substitutes for hydroxyl groups in phyllosilicates. The ratios of individual cations and hydrogen ion are governed by ionic exchange equilibria with hydrothermal minerals, probably smectite and chlorite. The equilibrium pH for the Reykjanes and Svartsengi geothermal waters is 5·5 and 5·1 respectively. Sea-water will become somewhat acid upon heating to more than about 300 °C and equilibration with basalt, the acidity increasing with temperature.


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