Caveats in defining the magmas parental to the mafic rocks of the Bushveld Complex, and the manner of their emplacement: review and commentary

2002 ◽  
Vol 66 (6) ◽  
pp. 815-832 ◽  
Author(s):  
H. V. Eales

Abstract The composition of magmas proposed as parental to the layered suite of the Bushveld Complex, and some models for the manner of their emplacement, are reviewed briefly. Included are some contributions published in South Africa, with which overseas readers might be less familiar. Emphasis is given to the broader features of the cumulates, and the contradictions raised by whole-rock compositional, Sr-isotopic, and trace-element data that cloud their correlation with proposed parental magmas. It is concluded that the Lower, Critical and Main Zones are the derivatives of only two primary magmatic lineages, while a third was added to residual liquids from which the layered rocks above the Pyroxenite Marker were formed. Excessive amounts of olivine and chromium in the cumulates of the Lower and Lower Critical Zones in the northern sector of the Western Limb can seemingly not be accounted for by the composition and volume of the putative magmas. This is attributed to (1) this sector being a proximal facies located close to the original feeder, and/or (2) crystal-charged magma batches, expelled from a lower magma chamber, being periodically injected into and dispersed within the liquids already in place in the Bushveld chamber. Thus, ongoing changes in the bulk composition of the liquids within the chamber would not be reflected in the rinds of earlier, chilled-facies rocks. The expulsion of significant volumes of liquid residua from the chamber during cumulate deposition is not ruled out.

Lithos ◽  
2018 ◽  
Vol 310-311 ◽  
pp. 332-341 ◽  
Author(s):  
T. Günther ◽  
K.M. Haase ◽  
M. Junge ◽  
T. Oberthür ◽  
D. Woelki ◽  
...  

1988 ◽  
Vol 52 (364) ◽  
pp. 81-89 ◽  
Author(s):  
R. Grant Cawthorn ◽  
Kevin L. Walsh

AbstractPhosphorus contents in cumulus rocks occurring close to the level of apatite appearance in the basic rocks of the Bushveld Complex, South Africa, provide a method of calculating the proportion of intercumulus component in these rocks. Previous experimental studies have accurately constrained the phosphorus content of magmas when apatite becomes stable. The ratio of the phosphorus content in the cumulates immediately below the appearance of apatite to this liquid composition defines the proportion of trapped liquid.Application of this method to rocks from the uppermost mafic rocks of the Bushveld Complex leads to the conclusion that there is from 1 to 6 per cent intercumulus component. Many of these rocks are multiphase cumulates and in such rocks estimation of intercumulus component from textural criteria is difficult.If crystals grow In situ on the floor of the magma chamber such small proportions of interstitial component can be produced without appealing to excessive diffusion and circulation of magma through an unconsolidated crystal pile. The geometry of the intrusion as well as its size might have a major influence on the proportion of the liquid ultimately solidifying within a cumulus rock.


1993 ◽  
Vol 106 (1-2) ◽  
pp. 171-186 ◽  
Author(s):  
D.L. Reid ◽  
R.G. Cawthorn ◽  
F.J. Kruger ◽  
M. Tredoux

2013 ◽  
Vol 107 (6) ◽  
pp. 915-942 ◽  
Author(s):  
Marina Yudovskaya ◽  
Judith Kinnaird ◽  
Anthony J. Naldrett ◽  
Nickolay Rodionov ◽  
Anton Antonov ◽  
...  

Minerals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 570
Author(s):  
Reiner Klemd ◽  
Andreas Beinlich ◽  
Matti Kern ◽  
Malte Junge ◽  
Laure Martin ◽  
...  

The Platreef, at the base of the northern limb of the Bushveld Complex in South Africa, hosts platinum-group element (PGE) mineralization in association with base-metal sulphides (BMS) and platinum-group minerals (PGM). However, whilst a magmatic origin of the stratiform mineralization of the upper Platreef has been widely confirmed, the processes responsible for the PGE and BMS mineralization and metasomatism of the host rocks in the Platreef are still under discussion. In order to contribute to the present discussion, we present an integrated petrographical, mineral-chemical, whole-rock trace- and major-element, sulphur- and neodymium-isotope, study of Platreef footwall clinopyroxenite drill core samples from Overysel, which is located in the northern sector of the northern Bushveld limb. A metasomatic transformation of magmatic pyroxenite units to non-magmatic clinopyroxenite is in accordance with the petrography and whole-rock chemical analysis. The whole-rock data display lower SiO2, FeO, Na2O and Cr (<1700 ppm), and higher CaO, concentrations in the here-studied footwall Platreef clinopyroxenite samples than primary magmatic Platreef pyroxenite and norite. The presence of capped globular sulphides in some samples, which display differentiation into pyrrhotite and pentlandite in the lower, and chalcopyrite in the upper part, is attributed to the fractional crystallization of a sulphide liquid, and a downward transport of the blebs. In situ sulphur (V-CDT) isotope BMS data show isotopic signatures (δ34S = 0.9 to 3.1 ‰; Δ33S = 0.09 to 0.32‰) close to or within the pristine magmatic range. Elevated (non-zero) Δ33S values are common for Bushveld magmas, indicating contamination by older, presumably crustal sulphur in an early stage chamber, whereas magmatic δ34S values suggest the absence of local crustal contamination during emplacement. This is in accordance with the εNd (2.06 Ga) (chondritic uniform reservoir (CHUR)) values, of −6.16 to −6.94, which are similar to those of the magmatic pyroxenite and norite of the Main Zone and the Platreef in the northern sector of the northern Bushveld limb. Base-metal sulphide textures and S–Se-ratios give evidence for a secondary S-loss during late- to post-magmatic hydrothermal alteration. The textural evidence, as well as the bulk S/Se ratios and sulphide S isotopes studies, suggest that the mineralization in both the less and the pervasively hydrothermally altered clinopyroxenite samples of Overysel are of magmatic origin. This is further supported by the PPGE (Rh, Pt, Pd) concentrations in the BMS and mass-balance calculations, in both of which large proportions of the whole-rock Pd and Rh are hosted by pentlandite, whereas Pt and the IPGE (Os, Ir, Ru) were interpreted to mainly occur in discrete PGM. However, the presence of pentlandite with variable PGE concentrations on the thin section scale may be related to variations in the S content, already at S-saturation during magmatic formation, and/or post-solidification mobilization and redistribution.


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