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SDLRC - Region: South Africa - Technical - 1990 onwards
The Sheahan Diamond Literature Reference Compilation - Technical Articles based on Major Region - South Africa: 1990 onwards
The Sheahan Diamond Literature Reference Compilation is compiled by Patricia Sheahan who publishes on a monthly basis a list of new scientific articles related to diamonds as well as media coverage and corporate announcements called the Sheahan Diamond Literature Service that is distributed as a free pdf to a list of followers. Pat has kindly agreed to allow her work to be made available as an online digital resource at Kaiser Research Online so that a broader community interested in diamonds and related geology can benefit. The references are for personal use information purposes only; when available a link is provided to an online location where the full article can be accessed or purchased directly. Reproduction of this compilation in part or in whole without permission from the Sheahan Diamond Literature Service is strictly prohibited. Return to Diamond Region Index
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
Each article reference in the SDLRC is tagged with one or more key words assigned by Pat Sheahan to highlight the main topics of the article. In addition most references have been tagged with one or more region words. In an effort to make it easier for users to track down articles related to a specific region, KRO has extracted these region words and developed a list of major region words presented in the Major Region Index to which individual region words used in the article reference have been assigned. Each individual Region Report contains in chronological order all the references with a region word associated with the Major Region word. Depending on the total for each reference type - technical, media and corporate - the references will be either in their own technical, media or corporate Region Report, or combined in a single report. Where there is a significant number of technical references there will be a technical report dedicated to the technical articles while the media and corporate references are combined in a separate region report. References that were added in the most recent monthly update are highlighted in yellow within the Region Report. The Major Region words have been defined by a scale system of "general", "continent", "country", "state or province" and "regional". Major Region words at the smaller scales have been created only when there are enough references to make isolating them worthwhile. References not tagged with a Region are excluded, and articles with a region word not matched with a Major Region show up in the "Unknown" report.
Kimberlite - diamondiferous
Lamproite - diamondiferous
Lamprophyre - diamondiferous
Other - diamondiferous
Kimberlite - non diamondiferous
Lamproite - non diamondiferous
Lamprophyre - non diamondiferous
Other - non diamondiferous
Kimberlite - unknown
Lamproite - unknown
Lamprophyre - unknown
Other - unknown
Future Mine
Current Mine
Former Mine
Click on icon for details about each occurrence. Works best with Google Chrome.
CITATION: Faure, S, 2010, World Kimberlites CONSOREM Database (Version 3), Consortium de Recherche en Exploration Minérale CONSOREM, Université du Québec à Montréal, Numerical Database on consorem.ca. NOTE: This publicly available database results of a compilation of other public databases, scientific and governmental publications and maps, and various data from exploration companies reports or Web sites, If you notice errors, have additional kimberlite localizations that should be included in this database, or have any comments and suggestions, please contact the author specifying the ID of the kimberlite: [email protected]
Middle-Proterozoic calc-alkaline, shoshonitic volcanism along the Eastern margin of the Namaqua Mobile Belt, South Africa- implications for tectonic evolution area
South African Journal of Geology, Vol. 93, No. 2, pp. 389-399
Review of 1989 international mineral industry activities.Brief mention Of diamonds in several countries. ie. South Africa, Zaire, Namibia, Angola, Guinea
Mining Engineering, Vol. 42, No. 7, July, pp. 665-675
South Africa, Democratic Republic of Congo, Namibia, Angola, Guinea
Cryptoexplosion structures, shock deformation and siderophileconcentration related to explosive venting of fluids associated with alkaline ultramafic magmas
Tectonophysics, Vol. 171, No. 1-4, January 1, pp. 303-335
Peraluminous metamorphic rocks from the Namaqualand Metamorphic Complex (South Africa): geochem. evidence for an exhalation related sed. origin in a Mid.Prot
Chemical Geology, Vol. 81, No. 3, January 30, pp. 221-240
Two cratons and an orogen. Excursion guidebook and review articles for afield workshop through selected Archean terranes of Swaziland, SouthAfrica, Zimbabwe
International Geological Correlation Programme (IGCP) Project 280- the oldest rocks on earth, available from Witwatersrand, approx. 400p. $ 40.00 United States incl. postage
Marine diamonds: the geological controls governing the marine and terrestrial diamond deposits occurring along the West Coast of the Republic of South Africa
Indiaqua, Industrial Diamond ANNUAL, 1991 pp. 53-56, 58-59
The stability of priderite, lindsleyite-mathiasite andyimengite-hawthornite under lower continental lithosphere conditions:experiments at 35 to 50 Kbar
Proceedings of Fifth International Kimberlite Conference held Araxa June 1991, Servico Geologico do Brasil (CPRM) Special, pp. 106-108
Comparison of Siberian and South African Diamondiferous kimberlites
Conference registration The Canadian Institute of Mining, Metallurgy and Petroleum (CIM) Xerox Tower Suite 1210, 3400 de Maissoneuve, Sept. 5-13, 1991 Fax 514 939-2714
Chronology of early Archean granite-greenstone evolution in the BarbertonMountainland, South Africa, based on precise dating by single zirconevaporation
Earth and Planetary Science Letters, Vol. 103, No. 1/4, April pp. 41-54
Argon isotope and halogen chemistry of phlogopite from South Africankimberlites: a combined step-heating, laser probe, electron microprobe and TEMstudy
Low -Ca garnet harzburgite xenoliths from southern Africa: abundance, composition, and bearing on the structure and evolution of the subcratoniclithosphere
Proceedings of Fifth International Kimberlite Conference held Araxa June 1991, Servico Geologico do Brasil (CPRM) Special, pp. 350-352
Variations in trapping temperatures and trace elements in peridotite-suite inclusions African diamonds- evidence 2 inclusion suites implications lithosphere stratigr
Contributions to Mineralogy and Petrology, Vol. 110, No. 1, March pp. 1-15
Phlogophite in the generation of olivine melilitites from Namaqualand, South Africa and implications for element fractionation processes in the uppermantle.
The track record for diamond indicator minerals: a summary of casehistories
The Canadian Mining and Metallurgical Bulletin (CIM Bulletin) , Annual Meeting Abstracts approximately 10 lines, Vol. 86, No. 968, March ABSTRACT p. 70
Lecuyer, C., Gruau, G., Anhaeusser, C.R., Fourcade, S.
The origin of fluids and the effects of metamorphism on the primary chemical compositions of Barberton komatiites: new evidence from geochemistry, isotopes
Economic Geology Research Unit, University of the Witwatersrand, Inf. Circular No. 272, 32p
Kimberlites and kimberlites or apples and orange(ite)s?
Mid-continent diamonds Geological Association of Canada (GAC)-Mineralogical Association of Canada (MAC) Symposium ABSTRACT volume, held Edmonton May, pp. 59-62.
Can differences in heat flow between east and southern Africa be easilyinterpreted? Implications for understanding regional variability in continentalheat
Tectonophysics, Vol. 219, pp. 257-272
South Africa
Heat Flow, Craton, Archean, Tanzanian, Mozambique Belt
Magmas and metasomites from the Proterozoic Premier kimberlite, SouthAfrica.
Mid-continent diamonds Geological Association of Canada (GAC)-Mineralogical Association of Canada (MAC) Symposium ABSTRACT volume, held Edmonton May, pp. 121-126.
Metasomatism of the southern African lithosphere as recorded by mantlegarnets.
Mid-continent diamonds Geological Association of Canada (GAC)-Mineralogical Association of Canada (MAC) Symposium ABSTRACT volume, held Edmonton May, pp. 127-132.
Coupled substitution of Hydrogen and minor elements in rutile and the implications of high OH contents in niobium and chromium rich rutile from the upper mantle.
American Mineralogist, Vol. 78, No. 11, 12, November-December pp. 1181-1191.
Isotopic disequilibration temperatures (Samarium/neodymium, Rubidium-Strontium) between mineral phases of coarse grained, low temperature garnet peridotites from Kimberley Floors.
Proceedings of Fifth International Kimberlite Conference, Vol. 1, pp. 354-365.
The geochemistry (platinum group elements (PGE)) in kimberlites and constraints of the nature platinum group elements (PGE) insubcratonic lithospheric mantle.
International Symposium Upper Mantle, Aug. 14-19, 1994, Extended abstracts pp. 73-75.
Bumby, A.J., Eriksson, P.G., Van der Merve, R., Brummer, J.J.
Shear zone controlled basins in the Blouberg area, Northern Province, syn and post tectonic sedimentation relating to 2.0 Ga reactivation of Limopo Belt.
Journal of African Earth Sciences, Vol. 33, No. 3-4,pp. 445-61.
Ultra high resolution seabed mapping using an AUV Dr. Ian Stephenson, Paul Nicholson, Annitta Attieh and Clayton Summers ( de Beers Marine) present case study
An infrared investigation of inclusion bearing diamonds from the Venetia kimberlite, northern province, South Africa: implications for diamonds from craton margin se
Contributions to Mineralogy and Petrology, Vol. 144, 1, Oct. pp. 98-108.
The Precambrian Earth, tempos and events, editors Eriksson, P.G., Altermann, W., Nelson, D.R., Mueller, W.U., Elsevier, Developments in Precambrian Geology No. 12, C
Canada, Nunavut, Africa, South Africa
Superplumes, igneous provinces, Baker Lake, Limpopo Bel
Gregoire, M., Tinguely, C., Bell, D.R., Le Roex, A.P.
Spinel lherzolite xenoliths from the Premier kimberlite ( Kaapvaal craton) South Africa: nature and evolution of the shallow upper mantle beneath Bushveld Complex.
Comtrasting Group I and Group II eclogite xenolith petrogenesis: petrological, trace element and isotopic evidence from eclogite, garnet websterite and akremite
Journal of Petrology, Vol. 46, 10, Oct. pp. 2059-2090.
Andreoli, M.A.G., Hart, R.J., Ashwal, L.D., Coetzee, H.
Correlations between U, Th content and metamorphic grade in the Western Namaqualand Belt, South Africa: with implications for radioactive heating of the crust.
High pressure intermediate temperature metamorphism in the southern Barbarton granitoid greenstone terrain, South Africa: a consequence of subduction driven ...
Benn, K., Mareschal, J-C., Condie, K.C. Archean Geodynamics and Environments, AGU Geophysical Monograph, No. 164, pp. 239-254.
Internal architecture of the Venetia K1 kimberlite: a new geological model and implications for kimberlite emplacement processes, Venetia mine, Limpopo RSA.
Paleomagnetism of the NeoArchean Pongola and Ventersdorp Supergroups and an appriasal of the 3.0 - 1.9 Ga apparent polar wander path of Kaapvaal Craton
New developments in diamond recovery and security procedures - preserving the dollars. Excellent pictoral- x-ray and optical sorting, material handling
Diamonds in Kimberley Symposium & Trade Show, Bristow and De Wit held August 23-24, Kimberley, South Africa, GSSA Diamond Workshop CD slides 1-94.
Archean to Proterzooic crustal evolution in the Central Zone of the Limpopo belt ( South Africa - Botswana ): constraints from combined U Pb and Lu Hf isotope analyses of zircon.
Archean to Proterzooic crustal evolution in the Central Zone of the Limpopo belt ( South Africa - Botswana ): constraints from combined U Pb and Lu Hf isotope analyses of zircon.
Caro, G., Bennett, V.C., Bourdon, B., Harrison, T.M., Von Quadt, A., Mojzsis, S.J., Harris, J.W.
Application of precise 142 Nd 144 Nd analysis of small samples to inclusions in diamonds ( Finsch SA ) and Hadean zircons ( Jack Hills, Western Australia).
Field evidence of eros-scale asteroids and impact forcing of Precambrian geodynamic episodes: Kaapvaal (South Africa) and Pilbara ( western Australia) cratons
Earth and Planetary Science Letters, Vol. 267, 3-4, pp. 559-570.
Hopp, J., Trieloff, M., Brey, G.P., Woodland, A.B., Simon, N.S.C., Wijbrans, J.R., Siebel, W., Reitter, E.
40 Ar 39 Ar ages of phlogopite in mantle xenoliths from South African kimberlites: evidence for metasomatic mantle impregnation during Kilbaran orogenic cycle.
Trumbull, R.B., Reid, D.L., De Beer, C., Van Acken, D., Romer, R.L.
Magmatism and continental breakup at the west margin of southern Africa: a geochemical comparison of dolerite dikes from northwestern Namibia and the Western Cape.
South African Journal of Geology, Vol. 110, 2-3, Sept. pp. 477-502.
Archean accretion and crustal evolution of the Kalahari craton: the zircon age and Hf isotope record of granitic rocks- Barberton/Swaziland to Francistown Arc.
Emplacement temperatures of pyroclastic and colcaniclastic deposits in kimberlite pipes in southern Africa: new constraints from paleomagnetic measurements
GAC/MAC/AGU Meeting held May 23-27 Toronto, Abstract only
Lithospheric structure, evolution and diamond prospectivity of the Rehoboth Terrane and western Kaapvaal Craton, southern Africa: constraints from broadband
Geochemical processes in peridotite xenoliths from the Premier diamond mine, South Africa: evidence -depletion and refertilization of subcratonic lithosphere.
Crustal structure of the Zimbabwe craton and the Limpopo belt of southern Africa: new constraints from seismic dat a and implications for its evolution.
South African Journal of Geology, Vol. 112, pp. 213-228.
Trace element chemistry of mineral inclusions in eclogitic diamonds from the Premier ( Cullinan) and Finsch kimberlites: implications for evolution mantle
Viljoen, K.S., Harris, J.W., Ivanic, T., Richardson, S.H., Whitehead, K.
Trace element geochemistry and Ni thermometry of garnet inclusions in peridotitic diamonds from Premier and Finsch, South Africa: implications - diamond formation
International Mineralogical Association meeting August Budapest, abstract p. 187.
Provenance and reconnaissance study of detrital zircons of the Paleozoic Cape Supergroup: revealing the interaction of Kalahari and Rio de la Plat a cratons.
International Journal of Earth Sciences, Vol. 100, 2, pp. 527-541.
Electrical conductivity of continental lithospheric mantle from integrated geophysical and petrological modeling: application to the Kaapvaal craton and Rehoboth
Journal of Geophysical Research, Vol. 116, B10, B10202
Petrology of the hypapbyssal kimberlite of the Kroonstad group II kimberlite (orangeite) cluster, South Africa: evolution of the magma within the cluster
The structural, metamorphic and temporal evolution of the country rocks surrounding Venetia mine, Limpopo belt: evidence for a single paleoproterozoic event
Precambrian Research, Vol. 186, 1-4, pp. 51-69.
Africa, South Africa
Tectonometamorphic - implications for a tectonic model
The nature of diamonds and their mineral inclusions: a study of diamonds from the PAnd a and Jagersfontein kimberlites and from placer deposits in Brazil.
Thesis, University of Alberta, Earth and Atmospheric Sciences, 214p.
Canada, Northwest Territories, Africa, South Africa, Brazil
Thesis - note availability based on request to author
Evolution of the South Africa mantle - a case study of garnet peridotites from the Finsch diamond mine ( Kaapvaal craton) part 2: multiple depletion and re-enrichment processes.
Eclogitic and peridotitic diamond formation(Kimberley Pool kimberlites, South Africa), as evidenced from C, N stable isotope: a main mantle derived source.
10th. International Kimberlite Conference Feb. 6-11, Bangalore India, Abstract
In situ U Pb dating and Sr Nd isotopic analysis of perovskite: constraints on the age and petrogenesis of the Kuruman kimberlite province, Kaapvaal Craton, South Africa.
Evolution of the South Africa mantle - a case study of garnet peridotites from the Finsch diamond mine ( Kaapvaal craton) part 1: inter-mineral trace element and isotopic equilibrium.
Mitchell, R.H., Scott Smith, B.H., Skinner, E.M.W.
Mineralogy of magmaclasts and interclast matrices of Kimberley-type pyroclastic kimberlites from the Kao, Letseng-La-Terae, Lethlakane and Premier kimberlite pipes of southern Africa.
10th. International Kimberlite Conference Held Bangalore India Feb. 6-11, Poster abstract
How structure and stress influence kimberlite emplacement.
Proceedings of the 10th. International Kimberlite Conference, Vol. 2, Special Issue of the Journal of the Geological Society of India,, Vol. 2, pp. 51-65.
Giuliani, A., Kamenetsky, V.S., Kendrick, M.A., Phillips, D., Wyatt, B.A., Maas, R.
Oxide, sulphide and carbonate minerals in a mantle polymict breccia: metasomatism by proto-kimberlite magmas, and relationship to the kimberlite megacrystic suite.
A structural analysis of the geophysical signature relationship between linear features and plug like bodies of sheets 2229AB and 2229AD in the Limpopo province, South Africa.
Konzett, J., Wirth, R., Hauzenberger, C., Whitehouse, M.
Two episodes of fluid migration in the Kaapvaal Craton lithospheric mantle associated with Cretaceous kimberlite activity: evidence from a harzburgite containing a unique assemblage of metasomatic zirconium-phases.
Palot, M., Pearson, D.G., Stern, R.A., Stachel, T., Harris, J.W.
Multiple growth events, processes and fluid sources involved in diamond genesis: a micro-analytical study of sulphide bearing diamonds from Finsch mine, RSA.
Geochimica et Cosmochimica Acta, Vol. 106, pp. 51-70.
On the iron isotope heterogeneity of lithospheric mantle xenoliths: implications for mantle metasomatism, the origin of basalts and the iron isotope composition of the Earth.
Contributions to Mineralogy and Petrology, Vol. 165, 6, pp. 1243-1258.
Geochronological and geochemical constraints on the formation and evolution of the mantle beneath the Kaapvaal craton: Lu Hf and Sm Nd systematics of subcalcic garnets from highly depleted peridotites.
Geochimica et Cosmochimica Acta, Vol. 113, pp. 1-20.
Relationships between oxygen fugacity and metasomatism in the Kaapvaal subcratonic mantle, represented by garnet peridotite xenoliths in the Wesselton kimberlite, South Africa.
Evolution of silicocrbonatite parental magmas to form the Phalaborwa igneous complex: a complex history of melting of multiple mantle sources, magma mingling, differentiation and magmatic exsolution.
Viljoen, K.S., Harris, J.W., Richardson, S.H., Gray, K.
Trace element chemistry of peridotitic garnets in diamonds from the Premier ( Cullinan) and Finsch kimberlites, South Africa: contrasting styles of mantle metasomatism.
Perceptions of the impact of board members' individual perspectives on the social and environmental performance of companies. ( Based on SA and not junior companies).
Journal of the South African Institute of Mining and Metallurgy, Vol. 114, Nov. pp. 957-969.
Abstract: We reconstruct the history of topographic growth in southern Africa on both sides of the Orange River valley from an integrated analysis of erosion surfaces, crustal deformation and climate change. First, we propose an inventory of erosion surfaces observed in the study area and classify them according to their most likely formative process, i.e. chemical weathering or mechanical erosion. Among the various land units observed we define a new class of landform: the pedivalley, which corresponds to a wide valley with a flat erosional floor. In the Orange River valley, we mapped three low-relief erosion surfaces, each bevelling a variety of lithologies. The oldest and most elevated is (1) a stripped etchplain evolving laterally into (2) a stepped pediplain bearing residual inselbergs; (3) a younger pediplain later formed in response to a more recent event of crustal deformation. These are all Cenozoic landforms: the etchplain is associated with a late Palaeocene to middle Eocene weathering event, and the two pediplains are older than the middle Miocene alluvial terraces of the Orange River. Landscape evolution was first driven by slow uplift (10 m/Ma), followed by a second interval of uplift involving a cumulative magnitude of at least 200 m. This event shaped the transition between the two pediplains and modified the drainage pattern. A final phase of uplift (magnitude: 60 m) occurred after the Middle Miocene and drove the incision of the lower terraces of the Orange River. Climate exerted a major control over the denudation process, and involved very humid conditions responsible for lateritic weathering, followed by more arid conditions, which promoted the formation of pedivalleys. Collectively, these produce pediplains.
Abstract: The Blue Moon diamond, discovered in January 2014 at the historic Cullinan mine in South Africa, is of significance from both trade and scientific perspectives. The 29.62 ct rough yielded a 12.03 ct Fancy Vivid blue, Internally Flawless gem. The authors were provided the opportunity to study this rare diamond at the Smithsonian Institution before it went on exhibit at the Natural History Museum of Los Angeles County. Infrared spectroscopy revealed that the amount of uncompensated boron in the diamond was 0.26 ± 0.04 ppm, consistent with measurements of several large type IIb blue diamonds previously studied. After exposure to short-wave ultraviolet light, the Blue Moon displayed orange-red phosphorescence that remained visible for up to 20 seconds. This observation was surprising, as orange-red phosphorescence is typically associated with diamonds of Indian origin, such as the Hope and the Wittelsbach-Graff. Time-resolved phosphorescence spectra exhibited peaks at 660 and 500 nm, typical for natural type II blue diamonds. As with most natural diamonds, the Blue Moon showed strain-induced birefringence.
Intracontinental anorogenic alkaline magmatism and carbonatites, associated mineral systems and the mantle plume connection. Brandberg, Erongo, Parana-Etendeka, Kruidfontein, Goudini
Gondwana Research, Vol. 27, 3, pp. 1181-1216.
Africa, East Africa, Namibia, South Africa, China, Australia
Abstract: The circular 625 km2 alkaline Pilanesberg Complex, South Africa, contains coeval eruptive and several distinctive intrusive syenitic and foyaitic components, concentrically arranged at the surface. However, owing to poor outcrop the relationships between the different intrusive rocks, and their shape in the third dimension cannot be convincingly determined in the field. The original interpretation was a laccolith, whereas later models suggested a funnel shape, and appealed to ring-dyke and cone-sheet emplacement mechanisms. However, the radial widths of these coarse-grained bodies are over 1 km and so cannot have been emplaced as ring dykes or cone sheets, which are usually quite thin and fine grained. Creating the space for emplacement and removal of pre-existing country rocks for each postulated subsequent intrusive event presents a major challenge to this latter hypothesis. Extensive previously published and new field relationships are re-evaluated here to suggest that the body is a gently inward-dipping sheet and that subsequent injections of magma merely pumped up an existing and evolving magma chamber rather than intruded into solid rocks. A Bouguer gravity anomaly model is presented that supports the concept of a shallow, flat-bottomed body rather than one that continues to significant depth. There are many analogies with the Kangerlussuaq Intrusion, Greenland.
GSA Annual Meeting, Paper 131-14, 1p. Abstract only
Africa, South Africa
Carbonatite
Abstract: Petrologic and geochemical data for carbonatites and associated alkaline igneous rocks are presented for the Zandkopsdrift Carbonatite Complex, Namaqualand. The samples included in this study are relatively fresh, collected by coring at depths of >70 m below the weathered cap zone. The Zandkopsdrift complex is the only locality in the province known to contain significant carbonatite. The carbonatites studied are calico-, ferro- and silico- carbonatites, based on mineralogy, texture, and major element composition. They have low to moderate Mg-numbers (35-65), variable MgO contents (1.2-8.50 wt.%) and high atomic Ca/Ca+Mg (0.73-0.97), indicating that they are not likely simple mantle melts. The carbonatites contain significant apatite, magnetite, pyrochlore and phlogopite. Zandkopsdrift also contains significant amounts of aillikite and olivine melilitite. These rocks have relatively low SiO2 (25-31 wt.%) and Al2O3 (5.3- 6.1 wt.%), high K2O (6-6.3 wt.%) and TiO2 (5.6-9.5 wt.%) and moderate Mg numbers (51-58). ?18O and ?13C isotopes were measured for carbonatites and aillikites. ?13CPDB values are close to those expected for mantle-derived carbonatites (-3.9 to -8.83), while the ?18OSMOW values are significantly higher (+13. 25 to 21.84‰). The high ?18O value observed in carbonatites and aillikites is most likely attributable to secondary alteration by hydrous/hydrothermal fluids. This supports the inference that the Zandkopsdrift carbonatite is magmatic in origin but was later affected by secondary alteration which resulted in the elevated O stable isotopes. The ‘mantle-like’ ?13C is inconsistent with significant assimilation of C-bearing crustal rocks. Chondrite-normalised REE contents in the carbonatites are 2400 to 10,600 for La and 36 to 170 for Lu. The high REE contents of the carbonatites are most likely due to a combination of a source metasomatised by a highly LREE-enriched agent, as well as significant magmatic differentiation. The relatively fractionated composition of the Zandkopsdrift aillikites and melilitites is also consistent with this hypothesis. We propose that the Zandkopsdrift carbonatites were most likely formed by either immiscible liquid separation from or fractional crystallization of a moderately fractionated, carbonate-rich silicate parental magma.
Session No. 131--Booth# 338
Deep-seated magmatism, its sources and plumes, Proceedings of XIII International Workshop held 2014., Vol. 2014, pp. 178-202.
Africa, South Africa, Russia, Yakutia
Deposit - Dike Newlands, Nyurbinskaya
Abstract: Green garnets occur in concentrates of diamondiferous kimberlite bodies in Yakutia (Udachnaya, Mir, etc.), South Africa (Newlands, Bellsbank), Venezuela (Guaniamo sills), and Canada (Mud Lake field). Mantle xenoliths of rocks containing such garnets are very rare. We found peridotite xenoliths with green garnet in situ in kimberlites of the Newlands dike. Xenoliths are irregular in form, 4.5*1.9 cm, 1.5*0.8 cm, and 1.0*0.5 cm in size, and have similar modal compositions: gar(70)+ol(28)+sp(2), gar(9)+ol(90)+sp(1) and gar(50)+ol(30)+sp(20). Rock texture is medium-crystalline, while structure is massive. We also identified a garnet macrocryst of 0.5*0.4 cm in size with a pale green kelyphytic rim. Garnet composition in the studied samples is quite constant and is characterized by the high Cr2O3 content (10.94-11.99%) and CaO content (19.52-24.94%) at the reduced contents of TiO2 (0.24-0.52%). The chrome spinel is high Cr2O3 (55%) content and the low TiO2 (0.5-0.6%) content. Olivine is high-Mg (Fo95), but elevated CaO content (0.09%). Isotopic composition of oxygen in garnet (?18O = 4.05-4.25 pm) and olivine (?18O = 4.91 pm) differs drastically from the mantle values. Rb-Sr and Sm-Nd isotopic composition show the relatively "young" model age of the sample relative to the depleted mantle (1.78 billion years), the age of formation of this rocks is also relatively "young" - probable mezoproterozoic. In kimberlites and placers of the Nyurbinskaya pipe (Nakyn field, Yakutia) there are 4 green garnet grains of 0.5-2.0 mm in size, including one intergrowth gar+sp. Most garnets are characterized by the higher CaO (18.06-22.87%) and TiO2 (1.46, 1.65, 1.75%) contents not noted before for similar garnets. Studied green garnets have the similar "sine wave" type of REE distribution for low-Ti garnets and a "raised" type of REE distribution with enrichment in medium and light REE for high-Ti garnet.
All green garnets are characterized by an increased content of light REE and Sc. High-Ti garnets are characterized by an increased content of light and middle REE, as well as titanium, and a particularly sharply increased content of Zr (!). Paragenesis ol+sp is formed at 805oand 23.4 kbar, and paragenesis ol+gar is formed at 1080oand 23.8 kbar. The rocks are characterized by nonequilibrium paragenesis ol+sp+gar and formation at moderate depths (80-90 km) under conditions of high heat flow (52-55 mW/m2). Judging from modal composition of studied xenoliths (absence of clinopyroxene), variations in chemical compositions and trace element compositions, relatively "young" model age and non-mantle isotopy of oxygen in garnets, these rocks are not "wehrlites" and likely represent metasomatic rocks such as uvarovite-chromite veins or schlierens at the moderate depths of upper mantle - it is similar to uvarovite-chromite veins of the metasomatic or a hydrothermal origin in the crustal serpentinites.
South African Journal of Geology, Vol. 118, 3, pp. 225-248.
Africa, South Africa
Geophysics - seismics
Abstract: Here we present a comprehensive depth and thickness map of the main Karoo and Cape Basins using borehole and reflection seismic data. The depth to the Whitehill Formation, which is the focus of current shale gas interest within the Karoo, is also mapped. Change: The deepest part of the basin is in the south, along the northern boundary of the Cape Fold Belt (~4000 m in the southwest Karoo and ~5000 m in the southeast; ~5500 to 6000 m sediment thickness). The Whitehill Formation along this boundary reaches a depth of ~3000 m in the southwest and ~4000 m in the southeast. Limited borehole data in the southeastern Karoo show a broad deepening of the basin here compared to the southwestern Karoo. In the southeast near East London faulting has resulted in deepening of the basin close to the coast, with the Whitehill Formation deepening to over ~5000 km. Seismic and borehole data show that the Cape Supergroup pinches out below the Karoo Basin around Beaufort West and Graaff-Reinet in the southern Karoo (32.6°S for the Bokkeveld and 32.4°S for the Table Mountain Group). The Cape Supergroup reaches thicknesses of around 4 km in the south. The gravity effect of these sediments does not account for the Cape Isostatic Anomaly (CIA) in the southern part of the Karoo Basin near Willowmore and Steytlerville, i.e., an ~45 mGal Bouguer gravity low. A refraction seismic profile over the anomaly shows this region is associated with a large volume of low velocity/density shallow sediments (4.5 m/s2, 2500 kg/m3), as well as a low velocity/density anomaly associated with a normal fault and the Klein Winterhoek Thrust Fault (5.5 m/s2, 2650 kg/m3). These low density shallow sediments are explained by uplift of Karoo and Cape sediments of ~2 km or greater that is evident on Soekor reflection seismic data. This deformation has brought lower density shales (1800 to 2650 kg/m3) of the Ecca Group closer to the surface. These shallower features along with a deeper lower crust in this region (6.5 m/s2, 2900 kg/m3) are interpreted to account for the CIA.
Earth and Planetary Science Letters, Vol. 431, pp. 274-286.
Africa, South Africa
Deposit - Lace
Abstract: Major- and trace-element compositions of eclogite and pyroxenite xenoliths of ?2.5 Ga age (in situ Pb-Pb data on clinopyroxene) from the Lace kimberlite on the Kaapvaal craton were investigated in order to constrain: (1) the nature and evolution of their protoliths; (2) the extent to which they preserve information on the state of the asthenospheric mantle source that gave rise to their low-pressure protoliths; and (3) the effect of their deep recycling on the radiogenic isotope evolution of the convecting mantle. Their elemental relationships are consistent with low-pressure fractionation of olivine ± plagioclase and clinopyroxene during oceanic crust formation, whereby the residual melt was enriched in rare-earth elements (REE), high field-strength elements and Y, producing inverse correlations of ?REE with the size of Eu- and Sr-anomalies. LREE-depletion may indicate loss of on average 20% of a partial melt upon subduction and metamorphism (eclogitisation) of oceanic crust, which did not, however, contribute to juvenile growth of continental crust. The eclogites have median Sm/Nd (0.40) and Lu/Hf (0.27) similar to Depleted Mantle, and lower U/Pb (0.02) and Th/Pb (0.02). If deeply subducted, these rocks cannot explain unradiogenic Nd and Hf, and radiogenic Pb isotope compositions in the sources of some modern ocean island basalts. Low incompatible trace-element contents similar to picrites, and Yb concentrations at a given TiO2 content similar to modern MORB, indicate derivation of the protoliths by average melt fractions of ?0.20-0.25?0.20-0.25 that left a spinel peridotite residue at pressures ?2.5 to 3.0 GPa. This shallow intersection of the peridotite solidus suggests moderate Archaean ambient mantle potential temperatures of ?1420 to 1470?°C. Samples filtered for clinopyroxene fractionation and metasomatism have V/Sc (4.7±1.24.7±1.2; n=11n=11) indicating lower fO2fO2 (?1.9 relative to the fayalite-magnetite-quartz buffer=?FMQbuffer=?FMQ) than modern MORB. This is in part due to the higher average melt extraction pressure (?1.5 GPa) during formation of their crustal protoliths. Extrapolation to 1 GPa, similar to the average pressure of present-day MORB generation, yields ?FMQ of ?1.7±1.1?1.7±1.1, corresponding to Fe3+# of 0.07±0.040.07±0.04. If these results are correct, they suggest an Archaean ambient mantle more reducing than at present, with implications for the speciation of volatiles, which affects the mantle solidus and the composition of volcanic gases. This has implications for the Archaean atmospheric redox evolution and the recycling of carbon and other volatiles.
Abstract: Everyday international political economy (EIPE) offers an opportunity to rethink the role of individuals and citizenry in shaping governance of natural resources. In South Africa, significant progress has been made by government in re-shaping water governance since the end of apartheid in the early 1990s. The role of government in water governance and water politics has thus been emphasised to a large degree. This study looks at historical material to assess the role that water politics and EIPE has played in shaping the use and management of water resources in the country. Case studies are analysed of two quaternary catchments, A63E and A71L in the Limpopo River Basin, to show how everyday actions by different actors has shaped the current waterscape in the basin. Four events, namely, the politics of the Middle Iron Age State at Mapungubwe; the development of the Mapungubwe National Park and World Heritage Site; the management of water for the De Beers Venetia Diamond Mine; and the establishment of the Coal of Africa Limited colliery are discussed in terms of the agential power at play during each event. The conclusions of the study are that EIPE and reflexive agential power are important factors in water governance that can sometimes be ignored through neoliberal institutionalism. In the current and future governance of water in South Africa they can offer an alternative view of the role and importance of actors and pathways for development.
Abstract: Garnets from kimberlite-hosted mantle and a few xenoliths from the lower crust were investigated for water, major, minor, and trace elements. Xenoliths from the mantle comprise pyroxenite, eclogite, alkremite, and peridotite, and crustal xenoliths are mafic high-pressure granulites. Samples from South Africa, Lesotho, and Namibia comprise two principal settings, Kaapvaal Craton (‘on craton’) and Rehoboth terrane (‘off craton’). The composition of garnet depends on rock type but is unrelated to the setting, except for Ti and Cr. In garnets from ‘off craton’ mantle xenoliths, Ti positively correlates with Cr whereas those from ‘on craton’ samples reveal a negative correlation between both elements. Rare earth element patterns indicative of a metasomatic overprint are observed in garnets from both settings, especially in eclogitic garnet. Water contents in garnet are low and range from <1 to about 40 ppm. No setting-related difference occurs, but a weak correlation between water and rock type exists. Water contents in garnets from eclogite and mafic granulite are lower than those in pyroxenite, alkremite, and peridotite. All garnets are water under-saturated, i.e. they do not contain the maximum amount of water that can be accommodated in the mineral structure. Cratonic and non-cratonic samples also show the same characteristics in the infrared (IR) absorption spectra. An absorption band at 3650 cm-1 is typical for most mantle garnets. Bands at 3520 and 3570 cm-1 are present only in TiO2-rich garnets from the Rehoboth terrane and are ascribed to a Ti-related hydrogen substitution. A number of garnets, especially from the Kaapvaal Craton, contain molecular water in addition to structural water. Molecular water is inhomogeneously distributed at grain scale pointing to local interaction with fluid and to disequilibrium at grain scale. These garnets consistently reveal either submicroscopic hydrous phases or additional IR bands at 3630 and 3610-3600 cm-1 caused by structural water. Both features do not occur in garnets in which molecular water is absent. The observations imply (i) relatively late introduction of fluid, at least in cases where hydrous phases formed, and (ii) a relatively dry environment because only water-deficient garnets are able to incorporate additional structural water. Most importantly, they imply (iii) that the low water contents are primary and not due to water loss during upward transport. This late water influx is not responsible for the metasomatic overprint indicated by garnet REE patterns. The results of this study suggest dry conditions in the lithosphere, including mantle and crustal sections of both the Kaapvaal Craton (‘on craton’) and the Rehoboth terrane (‘off craton’). If the low water contents contributed to the stabilization of the Kaapvaal cratonic root (Peslier et al., 2010) the same should apply to the Rehoboth lithosphere where the same variety of rock types occurs. The extremely low water contents in eclogite relative to pyroxenite may be explained by an oceanic crust origin of the eclogites. Subduction and partial melting would cause depletion of water and incompatible elements. The pyroxenites formed by crystal accumulation in the mantle and did not suffer melt depletion. Such a difference in origin can be reconciled with the low Ti contents in eclogitic garnet and the high Ti contents in pyroxenitic garnet.
Abstract: Kimberlite magmas are of economic and scientific importance because they represent the major host to diamonds and are probably the deepest magmas from continental regions. In addition, kimberlite magmas transport abundant mantle and crustal xenoliths, thus providing fundamental information on the composition of the sub-continental lithosphere. Despite their importance, the composition and ascent mechanism(s) of kimberlite melts remain poorly constrained. Phlogopite is one of the few minerals that preserves a history of fluid migration and magmatism in the mantle and crust and is therefore an invaluable petrogenetic indicator of kimberlite magma evolution. Here we present major and trace element compositional data for phlogopite from the Bultfontein kimberlite (Kimberley, South Africa; i.e. the kimberlite type-locality) and from entrained mantle xenoliths. Phlogopite macrocrysts (~ > 0.3-0.5 mm) and microcrysts (between ~ 0.1 and 0.3 mm) in the Bultfontein kimberlite display concentric compositional zoning patterns. The cores of these phlogopite grains exhibit compositions typical of phlogopite contained in peridotite mantle xenoliths. However, the rims of some grains show compositions analogous to kimberlite groundmass phlogopite (i.e. high Ti, Al and Ba; low Cr), whereas other rims and intermediate zones (between cores and rims) exhibit unusually elevated Cr and lower Al and Ba concentrations. The latter compositions are indistinguishable from matrix phlogopite in polymict breccia xenoliths (considered to represent failed kimberlite intrusions) and from Ti-rich overgrowth rims on phlogopite in other mantle xenoliths. Consequently, it is likely that these phlogopite grains crystallized from kimberlite melts and that the high Ti-Cr zones originated from earlier kimberlite melts at mantle depths. We postulate that successive pulses of ascending kimberlite magma progressively metasomatised the conduit along which later kimberlite pulses ascended, producing progressively decreasing interaction with the surrounding mantle rocks. In our view, these processes represent the fundamental mechanism of kimberlite magma ascent. Our study also indicates that, in addition to xenoliths/xenocrysts and magmatic phases, kimberlite rocks incorporate material crystallized at various mantle depths by previous kimberlite intrusions (mantle-derived ‘antecrysts’).
In situ oxygen isotope, major-, and trace element constraints on the metasomatic modification and crustal origin of a Diamondiferous eclogite from Roberts Victor, Kaapvaal Craton.
Geochimica et Cosmochimica Acta, in press available, 45p.
Abstract: Xenoliths of mantle peridotite have been sampled from four kimberlite intrusions, Melton Wold, Hebron, Uintjiesberg and Markt, emplaced through the Mesoproterozoic Namaqua-Natal Belt, along the southern border of the Kaapvaal Craton. Although many of the xenoliths are heavily altered, constituent clinopyroxene, garnet and phlogopite are fresh and have been analysed by electron microprobe for major elements and by laser ablation ICP-MS for trace elements. Primitive mantle-normalised REE abundances in clinopyroxene are all strongly LREE enriched and show a range of patterns including uniformly MREE-HREE sloped (referred to here as ‘normal’), sinusoidal and humped sinusoidal patterns. HREE abundances are extremely low (Yb = 0.3-0.06 × PM). REEN patterns in coexisting garnets show a similar range of patterns. When normalised to primitive mantle values, trace element patterns in some clinopyroxenes show strong relative depletion in Rb-Ba, Ta-Nb and Ti, with some samples also being relatively depleted in Zr-Hf. These trace element characteristics are indistinguishable from those found in clinopyroxene and garnet from peridotites from the adjacent cratonic mantle. Numerical modelling of reactive porous flow of an enriched metasomatic melt through a geochemically depleted peridotite matrix can account for the full range in observed REEN patterns. The relative depletion in Rb-Ba, Ta-Nb and Ti can be accounted for by an early crystallisation of phlogopite from the percolating melt. The relative depletion in Zr-Hf in some clinopyroxenes requires either zircon to crystallise in the proximal metasomatic assemblage, or metasomatism by a carbonatitic melt. Modelling results, together with the absence of clinopyroxene with depleted or even partially enriched REEN patterns, suggest that all clinopyroxene has been modally introduced through metasomatism into an initially highly depleted harzburgitic protolith. The range in Sr and Pb isotopic composition of the clinopyroxenes indicates regional metasomatism by melts of various compositions. The strong HREEN depletion is interpreted to reflect the effect of initial melt depletion in the early Proterozoic, with melting extending into the spinel stability field requiring an oceanic realm, and again later in the Mesoproterozoic (Namaqua Orogeny). The superimposed incompatible element enrichment indicates subsequent multiple enrichment events by rising alkaline melts similar in composition to kimberlite or ultramafic alkaline lamprophyre, possibly related to Mesozoic plume upwelling beneath the region, that reintroduced clinopyroxene into the depleted Proterozoic harzburgite protolith.
Abstract: Plate tectonics plays a vital role in the evolution of our planet. Geochemical analysis of Earth’s oldest continental crust suggests that subduction may have begun episodically about 3.8 to 3.2 billion years ago, during the early Archaean or perhaps more than 3.8 billion years ago, during the Hadean. Yet, mantle rocks record evidence for modern-style plate tectonics beginning only in the late Archaean, about 3 billion years ago. Here we analyse the nitrogen abundance, as well as the nitrogen and carbon isotopic signatures of Archaean placer diamonds from the Kaapvaal craton, South Africa, which formed in the upper mantle 3.1 to 3.5 billion years ago. We find that the diamonds have enriched nitrogen contents and isotopic compositions compared with typical mantle values. This nitrogen geochemical fingerprint could have been caused by contamination of the mantle by nitrogen-rich Archaean sediments. Furthermore, the carbon isotopic signature suggests that the diamonds formed by reduction of an oxidized fluid or melt. Assuming that the Archaean mantle was more reduced than the modern mantle, we argue that the oxidized components were introduced to the mantle by crustal recycling at subduction zones. We conclude, on the basis of evidence from mantle-derived diamonds, that modern-style plate tectonics operated as early as 3.5 billion years ago.
In situ oxygen-isotope, major, and trace element constraints on the metasomatic modification and crust origin of a Diamondiferous eclogite from Roberts Victor, Kaapvaal craton.
Geochimica et Cosmochimica Acta, Vol. 174, pp. 345-359.
Contributions to Mineralogy and Petrology, Vol. 171, 11, 24p.
Africa, South Africa
Deposit - Bellsbank
Abstract: An oceanic crustal origin is the commonly accepted paradigm for mantle-derived eclogites. However, the significance of the aluminous members of the eclogite suite, containing kyanite and corundum, has long been underrated and their role neglected in genetic models of cratonic evolution. Here, we present a geochemical and petrological study of a suite of kyanite- and corundum-bearing eclogites from the Bellsbank kimberlite, S. Africa, which originate from depths between 150 and 200 km. Although clearly of high-pressure provenance, these rocks had a low-pressure cumulative origin with plagioclase and olivine as major cumulate phases. This is shown by the very pronounced positive Eu anomalies, low REE abundances, and ? 18O values lower than the Earth’s mantle. Many chemical features are identical to modern-day troctolitic cumulates including a light REE depletion akin to MORB, but there are also distinguishing features in that the eclogites are richer in Na, Fe, and Ni. Two of the eclogites have a minimum age of ~3.2 Ga, defined by the extremely unradiogenic 87Sr/86Sr (0.7007) in clinopyroxene. Phase equilibria indicate that the parent melts were formed by partial melting below an Archean volcanic center that generated (alkali-)picritic to high-alumina tholeiitic melts from a mantle whose oxygen fugacity was lower than today. Fractional crystallization produced troctolites with immiscible sulfide melt droplets within the mafic crust. Instability of the mafic crust led to deep subduction and re-equilibration at 4 6 GPa. Phase relationships plus the presence of a sample with appreciable modal corundum but no Eu anomaly suggest that kyanite- and corundum-bearing eclogites may also originate as plagioclase-free, higher pressure cumulates of highly aluminous clinopyroxene, spinel, and olivine. This is consistent with the crystallizing phase assemblage from an olivine tholeiitic to picritic magma deeper in the Archean oceanic crust or uppermost mantle. We postulate that the magmatic and subduction processes driving modern plate tectonics already existed in the Meso- to Early Archean.
Geochimica et Cosmochimica Acta, Vol. 179, pp. 156-176.
Africa, South Africa
Deposit - Lace
Abstract: Diamond- and kyanite-bearing eclogites from the Lace kimberlite on the Kaapvaal craton have common picritic to gabbroic oceanic protoliths with bimineralic eclogites, lying on arrays of Eu? and ?REE that are consistent with accumulation and fractionation of plagioclase and olivine. However, they also show significant compositional differences, such as more grossular-rich garnet and aluminous clinopyroxene (cpx), which require the operation of additional processes. Their nature is elucidated using mineral major- and trace-element compositions, as well as Sr isotope ratios determined by in situ techniques.Highly variable major-element compositions across the co-genetic eclogite suites exert a strong effect on the trace-element distribution between garnet and cpx, whereby Sc, Ge, Sr, Y, Cd, REE, Th and U partition more strongly into garnet with increasing grossular-content. Thus, significant differences between the trace-element compositions of garnet can ensue from crystal-chemical effects alone, making their use as petrogenetic indicators potentially ambiguous. After correcting for these compositional effects, garnet in kyanite-/diamond eclogites, and in eclogites devoid of accessory minerals but with similar signatures, shows depletion (or dilution) in Sc, Ge, Y, In, Zr, Hf and the HREE, and enrichment in the LREE and Th compared to garnet in bimineralic eclogites. This is interpreted as the signature of a pelite-derived melt, which was transferred by addition of aluminous cpx that later exsolved kyanite and garnet, as observed in other aluminous eclogite suites. Continental input can explain initial (at 2.9 Ga) 87Sr/86Sr ? 0.714 measured in cpx in eleven samples with low 87Rb/86Sr (<0.01). The association of diamond with kyanite suggests that diamond formation is also linked to this event, possibly due to diamond formation by oxidation of reduced carbon, such as methane, and attendant reduction of Fe3+ in garnet. This model of sediment melt-oceanic crust interaction reconciles evidence for both low- and high-pressure igneous processes in some aluminous eclogites. We suggest that a subduction mélange is a favourable setting for the transfer of a sediment-derived signature into oceanic crust, leading to formation of diamondiferous kyanite-eclogites from bimineralic eclogites. Diapirism, fluxed by the presence of partial melt, may have facilitated dispersal of the eclogites in the lithosphere column, consistent with their widely varying equilibration pressures ranging from ?5 to 8 GPa.
Abstract: The lack of consensus on the possible range of initial kimberlite melt compositions and their evolution as they ascend through and interact with mantle and crustal wall rocks, hampers a complete understanding of kimberlite petrogenesis. Attempts to resolve these issues are complicated by the fact that kimberlite rocks are mixtures of magmatic, xenocrystic and antecrystic components and, hence, are not directly representative of their parental melt composition. Furthermore, there is a lack of direct evidence of the assimilation processes that may characterise kimberlitic melts during ascent, which makes understanding their melt evolution difficult. In this contribution we provide novel constraints on the interaction between precursor kimberlite melts and lithospheric mantle wall rocks. We present detailed textural and geochemical data for a carbonate-rich vein assemblage that traverses a garnet wehrlite xenolith [equilibrated at ~ 1060 °C and 43 kbar (~ 140-145 km)] from the Bultfontein kimberlite (Kimberley, South Africa). This vein assemblage is dominated by Ca-Mg carbonates, with subordinate oxide minerals, olivine, sulphides, and apatite. Vein phases have highly variable compositions indicating formation under disequilibrium conditions. Primary inclusions in the vein minerals and secondary inclusion trails in host wehrlite minerals contain abundant alkali-bearing phases (e.g., Na-K bearing carbonates, Mg-freudenbergite, Na-bearing apatite and phlogopite). The Sr-isotope composition of vein carbonates overlaps those of groundmass calcite from the Bultfontein kimberlite, as well as perovskite from the other kimberlites in the Kimberley area. Clinopyroxene and garnet in the host wehrlite are resorbed and have Si-rich reaction mantles where in contact with the carbonate-rich veins. Within some veins, the carbonates occur as droplet-like, globular segregations, separated from a similarly shaped Si-rich phase by a thin meniscus of Mg-magnetite. These textures are interpreted to represent immiscibility between carbonate and silicate melts. The preservation of reaction mantles, immiscibility textures and disequilibrium in the vein assemblage, suggests quenching, probably triggered by entrainment and rapid transport toward the Earth's surface in the host kimberlite magma. Based on the Sr-isotope systematics of vein carbonate minerals, and the close temporal relationship between carbonate-rich metasomatism and kimberlite magmatism, we suggest that the carbonate-rich vein assemblage was produced by the interaction between a melt genetically related to the Bultfontein kimberlite and wehrlitic mantle wall rock. If correct, this unique xenolith sample provides a rare snapshot of the assimilation processes that might characterise parental kimberlite melts during their ascent through the lithospheric mantle.
The Orange and Riet River alluvial diamond deposits in the vicinity of Douglas, Northern Cape Province: geology, evaluation, and exploitation of unique South African large diamond producing deposits.
IGC 35th., Session Mineral Exploration 1p. Abstract
Abstract: Reversed-zoned olivines (Fe-richer cores compared to rims), appear to be ubiquitous in kimberlites with a wide distribution. These olivines generally comprise a subordinate population relative to the dominant normally zoned olivines. However, they are notably more abundant in the megacryst-rich mid-Cretaceous Monastery and early Proterozoic Colossus kimberlites, located on the Kaapvaal and Zimbabwe cratons, respectively. The reverse-zoned olivines at these two localities define compositional fields that are closely similar to those for two olivine megacryst populations of the Cr-poor association which have been documented in the Monastery kimberlite. This points to a genetic link between megacrysts and the reversed zoned olivines. The ubiquitous, occurrence of the Fe-rich (relative to the field for rims) olivines in kimberlites with a wide geographic distribution in turn argues for an intimate link between megacrysts and the host kimberlite. Some large olivines have inclusions of rounded Cr-rich clinopyroxenes, garnets and/or spinel, characterized by fine-scale, erratic internal compositional zoning. Olivines with such chemically heterogeneous Cr-rich inclusions are not derived from disaggregated mantle peridotites, but are rather linked to the Cr-rich megacryst suite. Consequently, they cannot be used as evidence that cores of a majority of kimberlitic olivines are derived from disaggregated mantle peridotites.
Earth and Planetary Science Letters, Vol. 447, pp. 60-71.
Africa, South Africa
Deposit - Bultfontein
Abstract: Understanding the mineralogical controls on radiogenic chronometers is a fundamental aspect of all geochronological tools. As with other common dating tools, it has become increasingly clear that the Re -Os system can be impacted by multiple mineral formation events. The accessory and micrometric nature of the Re -Os-bearing minerals has made assessing this influence complex. This is especially evident in cratonic peridotites, where long residence times and multiple metasomatic events have created a complex melting and re-enrichment history. Here we investigate a harzburgitic peridotite from the Bultfontein kimberlite (South Africa) which contains sub-micron Pt -Fe-alloy inclusions within base metal sulphides (BMS). Through the combination of the focused ion beam lift-out technique and low blank mass spectrometry we were able to remove and analyse the Pt -Fe-alloy inclusions for their Re -Os composition and highly siderophile element (HSE) systematics. Six repeats of the whole-rock yield 187Os/188Os compositions of 0.10893 -0.10965, which correspond to Re depletion model ages (TRD) of 2.69 -2.79 Ga. The Os, Ir and Pt concentrations are slightly variable across the different digestions, whilst Pd and Re remain constant. The resulting HSE pattern is typical of cratonic peridotites displaying depleted Pt and Pd. The Pt -Fe-alloys have PUM-like 187Os/188Os compositions of 0.1294±24 (2-s.d.) and 0.1342±38, and exhibit a saw-tooth HSE pattern with enriched Re and Pt. In contrast, their BMS hosts have unradiogenic 187Os/188Os of 0.1084±6 and 0.1066±3, with TRD ages of 2.86 and 3.09 Ga, similar to the whole-rock systematics. The metasomatic origin of the BMS is supported by (i) the highly depleted nature of the mantle peridotite and (ii) their Ni-rich sulphide assemblage. Occurrence of Pt -Fe-alloys as inclusions within BMS grains demonstrates the genetic link between the BMS and Pt -Fe-alloys and argues for formation during a single but continuous event of silicate melt percolation. While the high solubility of HSE within sulphide mattes rules out early formation of the alloys from a S-undersaturated silicate melt and subsequent scavenging in a sulphide matte, the alignment of the Pt -Fe-alloy inclusions attests that they are exsolutions formed during the sub-solidus re-equilibration of the high temperature sulphide phases. The significant difference in 187Os/188Os composition between the included Pt -Fe-alloys and their BMS host can only be accounted for by different Re/Os. This suggests that the formation of Pt -Fe-alloy inclusions within a BMS can result in the fractionation of Re from Os. A survey experiment examining the partitioning of Re and Os confirmed this observation, with the Re/Os of the Pt -Fe-alloy inclusion up to ten times higher than the co-existing BMS. This fractionation implies that, when Re is present in the sulphide melt, the TRD ages of BMS containing alloy inclusions do not date the loss of Re due to partial melting, but rather its fractionation into the Pt -Fe-alloys. As such, BMS ages should be used with caution when dating ancient partial melting events.
Abstract: Blue diamonds are among the rarest and most valuable of naturally occurring gemstones. In this study, 12 rough naturally-sourced type IIb diamonds were subjected to HPHT annealing, three different irradiation energies, and then all were stepwise annealed from 200 °C to 1100 °C and the optical defects were documented by changes in phosphorescence and photoluminescence spectroscopy. Several optical features that are removed from natural type IIb diamonds by HPHT processing, such as 3H, 648.2 nm peak, 776.4 nm peak, and 660 nm band (red) phosphorescence, can be reintroduced into these diamonds with subsequent electron irradiation and annealing at low-to-moderate temperatures. The thermal stability of these centers along with their spatial distribution provided additional insights into their configuration and distinguished them from nitrogen-bearing diamonds.
Abstract: In this work we report for the first time the crystallographic orientations of olivine inclusions trapped in diamonds from the Kaapvaal craton (South Africa) determined by single-crystal X-ray diffraction, and analyze them together with all available data in the literature. The overall data set indicates no preferred orientation of the olivine inclusions with respect to their diamond hosts. However, diamonds containing multiple olivine inclusions sometimes show clusters of olivines with the same orientation in the same diamond host. We conclude that such clusters can only be interpreted as the remnants of single olivine crystals pre-dating the growth of the host diamonds.
Abstract: Diamonds form from fluids or melts circulating at depth in the Earth's mantle. Analysis of these fluids is possible if they remain entrapped in the diamond during its growth, but this is rarely observed in gem-quality stones. We provide the first evidence that typical mineral inclusions in gem-quality diamonds from the Siberian and Kaapvaal cratons are surrounded by a thin film of hydrous silicic fluid of maximum thickness 1.5 ?m. The fluid contains Si2O(OH)6, Si(OH)4, and molecular H2O and was identified using confocal micro-Raman spectroscopy and synchrotron-based X-ray tomographic microscopy. As the solid mineral inclusions have both peridotitic and eclogitic affinities and occur in two cratonic regions, our results demonstrate the strong connection between water-rich fluids and the growth of gem-quality lithospheric diamonds. The presence of the fluid films should be taken into account for a proper evaluation of H2O contents in the mantle based on H2O contents in solid inclusions and for a robust assessment of diamond formation pressures based on the residual pressures of the inclusions.
Abstract: U-Pb and Lu-Hf data are routinely used to trace detrital zircon in clastic sediments to their original source in crystalline bedrock (the protosource), to map out paths of sediment transport, and characterize large-scale processes of crustal evolution. For such data to have a provenance significance, a simple transport route from the protosource in which the zircon formed to its final site of deposition is needed. However, detrital zircon data from Phanerozoic sedimentary cover sequences in South Africa suggest that this “source to sink” relationship has been obscured by repeated events of sedimentary recycling. Phanerozoic sandstones (Cape Supergroup, Karoo Supergroup, Natal Group, Msikaba Formation) and unconsolidated, Cenozoic sands in South Africa share major detrital zircon fractions of late Mesoproterozoic (940-1120 Ma, ?Hf ? 0 to + 15) and Neoproterozoic age (470-720 Ma, ?Hf ? ? 10 to + 8). A Permian age fraction (240-280 Ma, ?Hf ? ? 8 to + 5) is prominent in sandstones from the upper part of the Karoo Supergroup. All of these sequences are dominated by material derived by recycling of older sedimentary rocks, and only the youngest, late Palaeozoic fraction has a clear provenance significance (Gondwanide orogen). The virtual absence of Archaean zircon is a striking feature in nearly all suites of detrital zircon studied in the region. This indicates that significant events in the crustal evolution history of southern African and western Gondwana are not represented in the detrital zircon record. South Africa provides us with a record of recycling of cover sequences throughout the Phanerozoic, and probably back into the Neoproterozoic, in which the “sink” of one sedimentary cycle will act as the “source” in subsequent cycles. In such a setting, detrital zircon may give information on sedimentary processes rather than on provenance.
Abstract: The origin of high topography in southern Africa is enigmatic. By comparing topography in different cratons, we demonstrate that in southern Africa both the Archean and Proterozoic blocks have surface elevation 500-700 m higher than in any other craton worldwide, except for the Tanzanian Craton. An unusually high topography may be caused by a low density (high depletion) of the cratonic lithospheric mantle and/or by the dynamic support of the mantle with origin below the depth of isostatic compensation (assumed here to be at the lithosphere base). We use free-board constraints to examine the relative contributions of the both factors to surface topography in the cratons of southern Africa. Our analysis takes advantage of the SASE seismic experiment which provided high resolution regional models of the crustal thickness. We calculate the model of density structure of the lithospheric mantle in southern Africa and show that it has an overall agreement with xenolith-based data for lithospheric terranes of different ages. Density of lithospheric mantle has significant short-wavelength variations in all tectonic blocks of southern Africa and has typical SPT values of ca. 3.37-3.41 g/cm3 in the Cape Fold and Namaqua-Natal fold belts, ca. 3.34-3.35 g/cm3 in the Proterozoic Okwa block and the Bushveld Intrusion Complex, ca. 3.34-3.37 g/cm3 in the Limpopo Belt, and ca. 3.32-3.33 g/cm3 in the Kaapvaal and southern Zimbabwe cratons.The results indicate that 0.5-1.0 km of surface topography, with the most likely value of ca. 0.5 km, cannot be explained by the lithosphere structure within the petrologically permitted range of mantle densities and requires the dynamic (or static) contribution from the sublithospheric mantle. Given a low amplitude of regional free air gravity anomalies (ca. + 20 mGal on average), we propose that mantle residual (dynamic) topography may be associated with the low-density region below the depth of isostatic compensation. A possible candidate is the low velocity layer between the lithospheric base and the mantle transition zone, where a temperature anomaly of 100-200 °C in a ca. 100-150 km thick layer may explain the observed reduction in Vs velocity and may produce ca. 0.5-1.0 km to the regional topographic uplift.
Abstract: We present a new regional model for the depth-averaged density structure of the cratonic lithospheric mantle in southern Africa constrained on a 30? × 30? grid and discuss it in relation to regional seismic models for the crust and upper mantle, geochemical data on kimberlite-hosted mantle xenoliths, and data on kimberlite ages and distribution. Our calculations of mantle density are based on free-board constraints, account for mantle contribution to surface topography of ca. 0.5-1.0 km, and have uncertainty ranging from ca. 0.01 g/cm3 for the Archean terrains to ca. 0.03 g/cm3 for the adjacent fold belts. We demonstrate that in southern Africa, the lithospheric mantle has a general trend in mantle density increase from Archean to younger lithospheric terranes. Density of the Kaapvaal mantle is typically cratonic, with a subtle difference between the eastern, more depleted, (3.31-3.33 g/cm3) and the western (3.32-3.34 g/cm3) blocks. The Witwatersrand basin and the Bushveld Intrusion Complex appear as distinct blocks with an increased mantle density (3.34-3.35 g/cm3) with values typical of Proterozoic rather than Archean mantle. We attribute a significantly increased mantle density in these tectonic units and beneath the Archean Limpopo belt (3.34-3.37 g/cm3) to melt-metasomatism with an addition of a basaltic component. The Proterozoic Kheis, Okwa, and Namaqua-Natal belts and the Western Cape Fold Belt with the late Proterozoic basement have an overall fertile mantle (ca. 3.37 g/cm3) with local (100-300 km across) low-density (down to 3.34 g/cm3) and high-density (up to 3.41 g/cm3) anomalies. High (3.40-3.42 g/cm3) mantle densities beneath the Eastern Cape Fold belt require the presence of a significant amount of eclogite in the mantle, such as associated with subducted oceanic slabs. We find a strong correlation between the calculated density of the lithospheric mantle, the crustal structure, the spatial pattern of kimberlites, and their emplacement ages. (1) Blocks with the lowest values of mantle density (ca. 3.30 g/cm3) are not sampled by kimberlites and may represent the "pristine" Archean mantle. (2) Young (< 90 Ma) Group I kimberlites sample mantle with higher density (3.35 ± 0.03 g/cm3) than the older Group II kimberlites (3.33 ± 0.01 g/cm3), but the results may be biased by incomplete information on kimberlite ages. (3) Diamondiferous kimberlites are characteristic of regions with a low-density cratonic mantle (3.32-3.35 g/cm3), while non-diamondiferous kimberlites sample mantle with a broad range of density values. (4) Kimberlite-rich regions have a strong seismic velocity contrast at the Moho, thin crust (35-40 km) and low-density (3.32-3.33 g/cm3) mantle, while kimberlite-poor regions have a transitional Moho, thick crust (40-50 km), and denser mantle (3.34-3.36 g/cm3). We explain this pattern by a lithosphere-scale (presumably, pre-kimberlite) magmatic event in kimberlite-poor regions, which affected the Moho sharpness and the crustal thickness through magmatic underplating and modified the composition and rheology of the lithospheric mantle to make it unfavorable for consequent kimberlite eruptions. (5) Density anomalies in the lithospheric mantle show inverse correlation with seismic Vp, Vs velocities at 100-150 km depth. However, this correlation is weaker than reported in experimental studies and indicates that density-velocity relationship in the cratonic mantle is strongly non-unique.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 14p.
Africa, South Africa
Deposit - Cullinan
Abstract: There are many underground mining software tools available to plan and schedule the development of underground mines. A shortfall of these tools is the optimization of the underground equipment and strategy in order to maximize the development rate. This paper will illustrate how the SimMine® software was used to maximize underground development at Petra Diamonds' Cullinan Diamond Mine. It will also determine the effect of various development strategies and equipment capacities on the underground development rate and pinpoint potential bottlenecks in the mine development cycle.
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The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 12p.
Africa, South Africa
Deposit - Venetia
Abstract: The nature of diamond deposits are such that most mineral resource reporting codes contain a sub-section unique to diamond estimation and classification. These codes identify a number of criteria which define the uniqueness of diamond deposits, including, the low and variable grade of diamond deposits; the particulate nature of diamonds which affects both size and revenue of individual particles and finally the inherent difficulties and uncertainties in the estimation of diamond resources. These criteria are expanded on to provide an overview of the estimation of kimberlite diamond deposits. Placer deposits have been excluded as they constitute a particularly complex example of particulate distributions. Diamond grade, typically of the order of parts per million (ppm), is dependent on the number of stones per unit volume or mass as well as the diamond size distribution while diamond revenue is dependent on size, model, colour and quality. These parameters of a discrete particle result in a conmlOdily which requires some unique estimation and modelling methodologies. For most commodities "grade" is a measure of concentration and is directly proportional to value. [n the case of diamonds however the same stone grade (e.g. stones per 100 tonnes) may have significantly different carat grades and revenue, depending on the characteristics of the individual stones (size, model, colour and quality). The De _Beers Consolidated Mines Venetia Mine is used as an example of diamond eslimation as well as to highlighl some propriety grade eslimation techniques. The mine has been sampled for grade using a number of different sample supports, from 36" diameter reverse circulation drillholes to micro diamond core drilling. De Beers Group Services (Ply) Lld (DBGS) have developed a technique of mixed (or multiple) support kriging which allows for the combination of samples of different sizes (and therefore grade distributions) in the estimation process. In addition DBGS have researched techniques of both global and local grade estimation using micro diamonds. The estimation of kimberlite diamond deposits has a number of unique components resulting from the discrete nature of the diamond distribution. It is however equally fundamentally important to understand exactly what the sampling data represents; the constraints Wlder which the data were coUected (e.g. bottom cut ofJ) and the adjustments necessary to ensure parity Page 73 The Southern African Institute of Mining and Metallurgy Diamonds - Source to Use 2010 DBush between and within sampling programmes as well as the likely metallurgical process III a production environment.
Abstract: Olivine is the dominant mineral present in kimberlite magmas; however, due to the volatile-rich nature of most kimberlites, they rarely survive late-stage serpentinisation. Here we present major and trace element data for a rare example of ultra-fresh olivine in a macrocrystic calcite kimberlite from the Benfontein kimberlite sill complex. Olivines are characterised by xenocrystic cores surrounded by multiple growth zones representing melt crystallisation and late-stage equilibration. Two distinct core populations are distinguished: Type 1) low Fo (88-89), Ni-rich, Ca- and Na-rich cores, interpreted here to be the result of carbonate-silicate metasomatism potentially as part of the earliest stages of kimberlite magmatism, and Type 2) high Fo (91-93), Ni-rich, low-Ca cores derived from a typical garnet peridotite mantle source. In both cases, the cores have transitional margins (Fo89-90) representing equilibration with a proto-kimberlite melt. Trace element concentrations, in particular Cr, of these transition zones suggest formation of the proto-kimberlite melt through assimilation of orthopyroxene from the surrounding garnet peridotite lithology. Trace element trends in the surrounding melt-zone olivine (Fo87-90) suggest evolution of the kimberlite through progressive olivine crystallisation. The final stages of olivine growth are represented by Fe-rich (Fo85) and P-rich olivine indicating kimberlite evolution to mafic compositions. Fine (< 60 ?m), Mg-rich olivine rims (Fo94-98) represent equilibration with the final stages of kimberlite evolution back to Fe-poor carbonatitic melts. We present a step-by-step model for kimberlite magma genesis and evolution from mantle to crust tracked by the chemistry of olivines in the Benfontein kimberlite. These steps include early stages of metasomatism and mantle assimilation followed by direct crystallisation of the kimberlite melt and late-stage equilibration with the evolved carbonatitic residual liquids. The Ca contents of the Type 1 xenocrystic olivines are the highest yet measured for mantle olivines, and do not overlap with any known mantle xenolith lithologies. These olivines likely represent an important stage of metasomatism directly related to the early stages of kimberlite melt ponding at the base of the lithospheric mantle.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 18p.
Africa, South Africa
Deposit - Finsch
Abstract: Finsch Mine is a kimberlite diamond mine located at Lime Acres in the Northern Cape Province of South Africa. The mine was founded in 1961 and started surface mining in 1964. Underground production commenced in 1990 using a modified blast-hole open stoping method for the mining of Blocks 1, 2 and 3. Block 4 is currently being mined as a block cave. The process of identifying and optimizing a method to mine the Block 5 orebody started in 1991, and in 2006 incline caving was identified as being technically feasible. This paper aims to document the process employed in developing this method by the Block 5 pre-feasibility team as well as discuss the technical challenges encountered during this process. The paper commences with a history of Finsch Mine and highlights the complex geology and threat of sidewall failure that prompted the decision to use block caving as the mining method for Block 4. A literature study of mines that implemented mining methods upon which the incline cave was conceptualized is then presented. These practices were then used to form the basis for the designs on which the initial geotechnical modelling was done and built upon through an iterative process of modelling and design changes. The ventilation of the mining area, initial productivity simulation results, and the applicability of automation and comminution processes in the incline cave are also presented. The paper concludes with an investigation into some of the challenges of the mining method, and shows that that incline caving is a technical option available for further investigation in determining the optimal mining method to be employed at Block 5, Finsch Diamond Mine.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 14p.
Africa, South Africa
Deposit - Finsch
Abstract: De Beers' Finsch Mine is situated in the Northern Cape ,province, 170 km northwest of Kimberley. The concentrator facility, designed and constructed by Bateman Engineering, was commissioned in 1967 and upgraded in 1979 using diamond liberation and extraction technology available at the time of design. Since then significant advances in diamond processing and technology have been made and these -have been incorporated into the new main treatment plant and recovery plant flowsheets, making diamond liberation and recovery from the Pre-1979 dumps a viable economic option at Finsch." Significant challenges were experienced as a result of the integration of new technology and its associated infrastructure into an existing plant. Major process flow changes were implemented during the execution phase of the project. The combined effect of these issues resulted in the project being overspent by 25% and the final handover to the Client was some 18 months later than originally planned." The paper highlights some of the difficulties experienced as a result of changes made during the execution phases of the project.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 12p.
Africa, South Africa
Deposit - Namaqualand mines
Abstract: Alluvial diamond deposits covered with a thick overburden cannot be explored effectively and mined profitably with the available conventional techniques. A novel directional drilling technique has been developed and site trials have been conducted at the e Beers Namaqualand Mines situated at the western coast of South Africa. This paper describes the technique developed as well as the results of the site trials. The main task of the project is to develop a tool and a supporting system to achieve a remote exploration and ore extraction method for inaccessible alluvial diamond deposits. The project involves the acquisition of a system, commissioning on-site and evaluating the information obtained during assessment. The project consists of the design - of certain tools and instrumentation for the system, investigations and desktop studies as well as development of the systems logistics. The operating philosophy of the system is based on the keyhole surgery principle. In this study a pilot hole was drilled first, starting from the surface with an inclination to reach deeply seated diamondiferous gravel layers, followed by drilling into a more or less horizontal gravel layer for a certain length and finally pointing-upwards reaching ground surface at a predetermined exit point. The pilot drill bit was then replaced with a larger diameter reamer/mining tool and an HDPE tail pipe was attached behind the reamer. The drill string was retracted back to enlarge the guide hole and flush the excavated ore to the surface through the tail pipe. The material flow in between the sections of the system was carefully measured to assess and record the gravel recovery rates. Several horizontal holes were drilled at preplanned drill paths to reach and follow the ore layer and the ore extraction was achieved by means of a reamer/mining tool. Principles of the concept have been proven viable in this investigation
Abstract: Kimberlitic magmaclasts are discrete ovoid magmatic fragments that formed prior to emplacement from disrupted kimberlite magma. To provide new constraints on the origin and evolution of the kimberlite melts, we document the mineralogy and petrography of a magmaclast recovered from one of the ca. 520 Ma Venetia kimberlites, South Africa. The sample (BI9883) has a sub-spherical shape and consists of a ~ 10 mm diameter central olivine macrocryst, surrounded by porphyritic kimberlite. The kimberlitic material consists of concentrically aligned, altered olivine phenocrysts, set in a crystalline groundmass of calcite, chromite, perovskite, phlogopite, apatite, ilmenite, titanite, sulphides, rutile and magnetite along with abundant alteration phases (i.e. serpentine, talc and secondary calcite). These features are typical of archetypal hypabyssal kimberlites. We examined primary fluid/melt inclusions in chromite, perovskite and apatite containing a diversity of daughter phases. Chromite and perovskite host polycrystalline inclusions containing abundant alkali-carbonates (i.e. enriched in K, Na, Ba, Sr), phosphates, Na-K chlorides, sulphides and equal to lesser quantities of olivine, phlogopite and pleonaste. In contrast, apatite hosts polycrystalline assemblages with abundant alkali-carbonates and Na-K chlorides and lesser amounts of olivine, monticellite and phlogopite. Numerous solid inclusions of shortite (Na2Ca2(CO3)3), Na-Sr-carbonates and apatite occur in groundmass calcite along with fluid inclusions containing daughter crystals of Na-carbonates and Na-chlorides. The primary inclusions in chromite, perovskite and apatite are considered to represent remnants of fluid(s)/melt(s) trapped during crystallisation of the host minerals, whereas the fluid inclusions in calcite are probably secondary in origin. The component proportions of these primary fluid/melt inclusions were estimated in an effort to constrain the composition of the evolving kimberlite melt. These estimates suggest melt evolution from a silicate-carbonate kimberlite melt that became increasingly enriched in carbonates, phosphates, alkalis and chlorides, in response to the fractional crystallisation of constituent minerals (i.e. olivine to apatite). The concentric alignment of crystals around the olivine kernel and ovoid shape of the magmaclast can be ascribed to the low viscosity of the kimberlite melt and rapid rotation whilst in a liquid or partial crystalline state, or to progressive layer-by-layer growth of the magmaclast. Although the mineralogy of our sample is similar to hypabyssal kimberlites worldwide, it differs from hypabyssal kimberlite units in the main Venetia pipes, which contain monticellite-phlogopite rich assemblages and segregationary matrix textures. Therefore magmaclast BI9883 probably originated from a batch of magma distinct from those that produced known hypabyssal units within the Venetia kimberlite cluster.-
Abstract: The Mesoproterozoic Pilanesberg Complex, South Africa, is built up by several distinct, ring-shaped intrusions of syenite and peralkaline nepheline syenite. A mildly peralkaline ((Na + K) / Al = 1.04–1.09), medium-to coarse grained nepheline syenite makes up the outermost ring in the southwestern part of the complex (“Matooster type white foyaite”). In this rock, mafic silicate minerals (amphibole, biotite, aegirine) and Ti-bearing minerals (ilmenite, astrophyllite, aenigmatite, lorenzenite, bafertisite, jinshajiangite) are interstitial to feldspar and nepheline, and define a series of mineral assemblages reflecting a change from a miaskitic crystallization regime (with Na-Ca amphibole, titanite and ilmenite) to increasingly agpaitic conditions (with arfvedsonite, aegirine, astrophyllite, aenigmatite, lorenzenite). The main driving force behind the evolution was an increase in peralkalinity of the trapped liquid, mainly by adcumulus growth of alkali feldspar and nepheline, which in the later stages of evolution was combined with increases in oxygen fugacity and water activity. Unlike in most other agpaitic rock complexes, Zr remained compatible in aegirine (and to some extent in amphibole) almost to the end of the process, when a hydrous zirconium silicate mineral (hilairite) crystallized as the only mineral in the rock having essential zirconium. The presence of minerals such as hilairite, bafertisite, jinshajiangite and a Na-REE-Sr rich apatite group mineral (fluorcaphite ?) in the latest assemblages suggests that the last remaining interstitial melt or fluid approached a hyperagpaitic composition. The isolated melt pockets in the Pilanesberg white foyaite follow a pattern of evolution that can be seen as a miniature analogue of the fractional crystallization processes controlling magma evolution in large, alkaline igneous rock complexes.-
Thesis, University of Pretoria, Ms Metallurgical Engineering 279p. Pdf
Africa, Angola, South Africa
Deposit - AC 56-5-1, Venetia Red
Abstract: Kimberlite is the host rock from which diamonds are mined. The mineralogical features for kimberlites vary greatly with country, origin, depth and type of kimberlite. Kimberlites can contain various clay species with some kimberlites containing predominantly clay minerals. The presence of these clay minerals in the ore can cause difficulty in dewatering due to high flocculant demand, poor supernatant clarity and low settling rates. Identifying critical parameters that can predict the settling behaviour of African kimberlite slurries will assist the process engineer to predict the settling behaviour of different kimberlite slurries. Especially identifying the kimberlites that will most likely not settle with normal flocculant dosage rates is useful. From first principles the settling of a particle is described by Stoke’s law which incorporates the density of the particle and size of the particle as the inherent particle variables. In this case density is assumed constant and therefore the size of particles influence the settling rate of particles to a great extent. This study therefore investigated the influence of particle size on settling rate and whether the particle size distribution showed correlation with settling rate when regression modelling was fitted on the data. Other variables that were tested for correlation with settling were pH when the kimberlite is mixed in water as well as various mineralogical features of the ore. Fitting a simple model to any of these properties or combinations of these properties was attempted which would allow for prediction of settling behaviour. The mineralogical features were classified by evaluating the mineral composition, fractional elemental analysis, cation exchange capacity and the exchangeable sodium percentage of the different kimberlites. These variables were tested as well as their settling behaviour with 18 different African kimberlite samples. The settling rate and slurry bed compaction during natural settling as well coagulant and flocculant assisted settling were measured for the kimberlite slurries. The best performing coagulant and flocculant for each kimberlite were combined to evaluate potential improvements in the settling rates and slurry bed compaction compared to current settling practices that only utilise flocculant additions. Especially the use of coagulant for kimberlites that did not show settling with only flocculants was evaluated. For these 18 kimberlites only 2 kimberlites did not settle with the use of flocculants with settling rates varying between 10.7m/h and 25m/h. Both these kimberlites also did not settle with the combination of coagulant and flocculant, but could only settle with only coagulant additions at settling rates of 1.9 m/h and 2.2 m/h. Regression analysis fitted to the settling rate investigated the influence of particle size, pH and mineralogical features on settling. For representation of the particle size two data points from the Particle Size Distribution (PSD) was utilised which represented the fine material and the coarser material. These two data points were taken at percentage passing 7.5 ?m and 75 ?m. Regression data for kimberlite with flocculant additions showed that particle size and the pH of the slurry were identified as significant parameters in predicting settling. The regression data showed a R2 of 0.78 for the settling rate and an adjusted R2 of 0.79 for the slurry bed depth.
Abstract: Magnesium and oxygen are critical elements in the solid Earth and hydrosphere. A better understanding of the combined behavior of Mg and O isotopes will refine their use as a tracer of geochemical processes and Earth evolution. In this study, the Mg-isotope compositions of garnet and omphacite separated from well-characterized xenolithic eclogites from the Roberts Victor kimberlite pipe (South Africa) have been measured by solution multi-collector ICP-MS. The reconstructed whole-rock ?26Mg values of Type I (metasomatized) eclogites range from ? 0.61‰ to ? 0.20‰ (Type IA) and from ? 0.60‰ to ? 0.30‰ (Type IB) (mean ? 0.43‰ ± 0.12‰), while ?26Mg of Type IIA (fresh, least metasomatized) eclogites ranges from ? 1.09‰ to ? 0.17‰ (mean ? 0.69‰ ± 0.41‰); a Type IIB (fresh, least metasomatized) has ?26Mg of ? 0.37‰. Oxygen-isotope compositions of garnet were analyzed in situ by SIMS (CAMECA 1280) and cross-checked by laser fluorination. Garnets have ?18O of 6.53‰ to 9.08‰ in Type IA, 6.14‰ to 6.65‰ in Type IB, and 2.34‰ to 2.91‰ in Type IIB. The variation of ?26Mg and ?18O in Type IA and IB eclogites is consistent with the previously proposed model for the evolution of these samples, based on major and trace elements and radiogenic isotopes. In this model, the protoliths (Type II eclogites) were metasomatized by carbonatitic to kimberlitic melts/fluids to produce first Type IA eclogites and then Type IB. Metasomatism has changed the O-isotope compositions, but the Mg-isotope compositions of Type IA are mainly controlled by the protoliths; those of Type IB eclogites reflect mixing between the protoliths and the kimberlitic melt/fluid. The combination of a large range of ?26Mg and low ?18O in Type II eclogites cannot be explained easily by seawater alteration of oceanic crust, interaction of carbonate/silicate sediments with oceanic crust, or partial melting of mafic rocks.
Abstract: Magmas forming large igneous provinces (LIP) on continents are generated by extensive melting in the deep crust and underlying mantle and associated with break-up of ancient supercontinents, followed by formation of a new basaltic crust in the mid-oceanic rifts. A lack of the unifying model in understanding the sources of LIP magmatism is justified by lithological and geochemical complexity of erupted magmas on local (e.g. a cross-section) and regional (a single and different LIP) scales. Moreover, the majority of LIP rocks do not fit general criteria for recognizing primary/primitive melts (i.e. < 8 wt% MgO and absence of high-Fo olivine phenocrysts). This study presents the mineralogical (olivine, Cr-spinel, orthopyroxene), geochemical (trace elements and Sr-Nd-Hf-Pb isotopes) and olivine-hosted melt inclusion compositional characteristics of a single primitive (16 wt% MgO), high-Ti (2.5 wt% TiO2) picrite with high-Mg olivine (up to 91 mol% Fo) from the Letaba Formation in the ~ 180 Ma Karoo LIP (south Africa). The olivine compositions (unusually high ?18O (6.17‰), high NiO (0.36-0.56 wt%) and low MnO and CaO (0.12-0.20 and 0.12-0.22 wt%, respectively)) are used to argue for a non-peridotitic mantle source. This is supported by the enrichment of the rock and melts in most incompatible trace elements and depletion in heavy rare earth elements (e.g. high Gd/Yb) that reflects residual garnet in the source of melting. The radiogenic isotopes resemble those of the model enriched mantle (EM-1) and further argue for a long-term enrichment of the source in incompatible trace elements. The enriched high-Ti compositions, strongly fractionated incompatible trace elements, presence of primitive olivine and high-Cr spinel in the Letaba picrites are closely matched by olivine-phyric rocks from the ~ 260 Ma Emeishan (Yongsheng area, SW China) and ~ 250 Ma Siberian (Maimecha-Kotuy region, N Siberia) LIPs. However, many other compositional parameters (e.g. trace element and ?18O compositions of olivine phenocrysts, Fe2 +/Fe3 + in Cr-spinel, Sr-Nd-Hf isotope ratios) only partially overlap or even diverge. We thus imply that parental melts of enriched picritic rocks with forsteritic olivine from three major continental igneous provinces - Karoo, Emeishan and Siberia cannot be assigned to a common mantle source and similar melting conditions. The Karoo picrites also exhibit some mineralogical and geochemical similarities with rocks and glasses in the south Atlantic Ridge and adjacent fracture zones. The geodynamic reconstructions of the continental plate motions since break-up of the Gondwanaland in the Jurassic support the current position of the source of the Karoo magmatism in the southernmost Atlantic. Co-occurrence of modern and recent anomalous rocks with normal mid-ocean ridge basalts in this region can be related to blocks/rafts of the ancient lithosphere, stranded in the ambient upper mantle and occasionally sampled by rifting-related decompressional melting.
Abstract: The petrogenesis of kimberlites commonly is obscured by interaction with hydrothermal fluids, including deuteric (late-magmatic) and/or groundwater components. To provide new constraints on the modification of kimberlite rocks during overprinting by such fluids and on the fractionation of kimberlite magmas during crystallisation, we have undertaken a detailed petrographic and geochemical study of a hypabyssal sample (BK) from the Bultfontein kimberlite (Kimberley, South Africa).
Journal of Structural Geology, Vol. 86, pp. 47-61.
Africa, South Africa
Deposit - Venetia
Abstract: The Beit Bridge Complex of the Central Zone (CZ) of the Limpopo Belt hosts the 519 ± 6 Ma Venetia kimberlite diatremes. Deformed shelf- or platform-type supracrustal sequences include the Mount Dowe, Malala Drift and Gumbu Groups, comprising quartzofeldspathic units, biotite-bearing gneiss, quartzite, metapelite, metacalcsilicate and ortho- and para-amphibolite. Previous studies define tectonometamorphic events at 3.3-3.1 Ga, 2.7-2.5 Ga and 2.04 Ga. Detailed structural mapping over 10 years highlights four deformation events at Venetia. Rules-based implicit 3D modelling in Leapfrog Geo provides an unprecedented insight into CZ ductile deformation and sheath folding. D1 juxtaposed gneisses against metasediments. D2 produced a pervasive axial planar foliation (S2) to isoclinal F2 folds. Sheared lithological contacts and S2 were refolded into regional, open, predominantly southward-verging, E-W trending F3 folds. Intrusion of a hornblendite protolith occurred at high angles to incipient S2. Constrictional-prolate D4 shows moderately NE-plunging azimuths defined by elongated hornblendite lenses, andalusite crystals in metapelite, crenulations in fuchsitic quartzite and sheath folding. D4 overlaps with a: 1) 2.03-2.01 Ga regional M3 metamorphic overprint; b) transpressional deformation at 2.2-1.9 Ga and c) 2.03 Ga transpressional, dextral shearing and thrusting around the CZ and d) formation of the Avoca, Bellavue and Baklykraal sheath folds and parallel lineations.
Journal of South African Institute of Mining and Metallurgy, Vol. 116, Aug. pp. 745-753.
Africa, South Africa
Deposit - Cullinan
Abstract: In 2012, Cullinan Diamond Mine began an expansion programme with the shaft deepening and development of access to the C-Cut 1 block at approximately 839 m below surface. The expansion programme is funded by a combination of bank loans and retained operating profit generated by the mine. Continuous production during deepening of the No. 1 Shaft, which is the rock hoisting shaft, was therefore critical for sustainability and efficiency as well as overall funding of the project. The deepening method, support design and verification, as well as learning outcomes pertaining to the extension of the No. 1 Shaft underneath the existing operating shaft are summarized, with emphasis on the importance of gaining some understanding of the shaft's host rock mass.
Journal of South African Institute of Mining and Metallurgy, Vol. 116, Apr. pp. 343-348.
Africa, South Africa
Deposit - Cullinan
Abstract: Near-infrared (NIR) spectroscopy sorting technology is incorporated in an automated optical mineral sorter that can discriminate between materials using the differences in characteristics when exposed to near-infrared radiation. During September 2014 to April 2015, a pilot plant that utilized NIR technology to discriminate between kimberlite and waste materials was commissioned to determine the viability of including this technology in the diamond winning process flow sheet at Cullinan Diamond Mine. The plant was used to minimize the waste content in the size fraction -70+35 mm that reports to the crushing section and then to the dense media separation process. This paper describes the initial test work, conducted at Mintek, that led to the decision to conduct a pilot-scale study. The mineralogical characterization of the feed and product streams to establish the sorting criteria and the operational data obtained during the pilot plant campaign are described. The results indicated a good possibility of discriminating between the kimberlite and waste material using NIR technology. However, the consistency of discrimination was not good enough to avoid the risk of potential diamond loss. Furthermore, a lower than expected availability of the machine reduced the throughput capabilities.
Abstract: In situ laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and electron probe microanalysis (EPMA) are used to characterize magnetite and ilmenite of the phoscorite-carbonatite association at Phalaborwa. We trace the behavior of the compatible elements for two different generations of magnetite related to (1) a magmatic stage, with variable Ti-V content, which pre-dates the copper mineralization, and (2) a late hydrothermal, low-Ti, low-temperature event, mostly post-dating sulfide formation. Magnetite is shown to be a robust petrogenetic indicator; no influence on its chemical composition is detected from the intergrowth with the accompanying phases, including the interaction with coexisting sulfides. High spatial resolution EPMA characterize the tiny late-stage hydrothermal magnetite veins, as well as the ilmenite granular and lamellar exsolutions mostly developed in the magnetite from the phoscorite. By combining geochemical data with geothermo-oxybarometry calculations for magnetite-ilmenite pairs, we infer that the most primitive magnetite probably formed at oxygen fugacity above the nickel nickel oxide (NNO) buffer, revealing an evolutionary trend of decreasing temperature and oxygen fugacity. Geochemical similarity exists between magnetite from phoscorite and carbonatite, thus supporting a common mantle source for the phoscorite-carbonatite association.
Geochimica et Cosmochimica Acta, Vol. 200, pp. 167-185.
Africa, South Africa, Russia
Metasomatism
Abstract: We present Mg and Fe isotopic data for whole rocks and separated minerals (olivine, clinopyroxene, orthopyroxene, garnet, and phlogopite) of garnet peridotites that equilibrated at depths of 134-186 km beneath the Kaapvaal and Siberian cratons. There is no clear difference in ?26Mg and ?56Fe of garnet peridotites from these two cratons. ?26Mg of whole rocks varies from ?0.243 to ?0.204 with an average of ?0.225 ± 0.037 (2?, n = 19), and ?56Fe from ?0.038‰ o 0.060 with an average of ?0.003 ± 0.068 (2?, n = 19). Both values are indistinguishable from the fertile upper mantle, indicating that there is no significant Mg-Fe isotopic difference between the shallow and deep upper mantle. The garnet peridotites from ancient cratons show ?26Mg similar to komatiites and basalts, further suggesting that there is no obvious Mg isotopic fractionation during different degrees of partial melting of deep mantle peridotites and komatiite formation. The precision of the Mg and Fe isotope data (±0.05 for ?26Mg and ?56Fe, 2?) allows us to distinguish inter-mineral isotopic fractionations. Olivines are in equilibrium with opx in terms of Mg and Fe isotopes. Garnets have the lowest ?26Mg and ?56Fe among the coexisting mantle minerals, suggesting the dominant control of crystal structure on the Mg-Fe isotopic compositions of garnets. Elemental compositions and mineralogy suggest that clinopyroxene and garnet were produced by later metasomatic processes as they are not in chemical equilibrium with olivine or orthopyroxene. This is consistent with the isotopic disequilibrium of Mg and Fe isotopes between orthopyroxene/olivine and garnet/clinopyroxene. Combined with one sample showing slightly heavy ?26Mg and much lighter ?56Fe, these disequilibrium features in the garnet peridotites reveal kinetic isotopic fractionation due to Fe-Mg inter-diffusion during reaction between peridotites and percolating melts in the Kaapvaal craton.
Abstract: In situ laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and electron probe microanalysis (EPMA) are used to characterize magnetite and ilmenite of the phoscorite-carbonatite association at Phalaborwa. We trace the behavior of the compatible elements for two different generations of magnetite related to (1) a magmatic stage, with variable Ti-V content, which pre-dates the copper mineralization, and (2) a late hydrothermal, low-Ti, low-temperature event, mostly post-dating sulfide formation. Magnetite is shown to be a robust petrogenetic indicator; no influence on its chemical composition is detected from the intergrowth with the accompanying phases, including the interaction with coexisting sulfides. High spatial resolution EPMA characterize the tiny late-stage hydrothermal magnetite veins, as well as the ilmenite granular and lamellar exsolutions mostly developed in the magnetite from the phoscorite. By combining geochemical data with geothermo-oxybarometry calculations for magnetite-ilmenite pairs, we infer that the most primitive magnetite probably formed at oxygen fugacity above the nickel nickel oxide (NNO) buffer, revealing an evolutionary trend of decreasing temperature and oxygen fugacity. Geochemical similarity exists between magnetite from phoscorite and carbonatite, thus supporting a common mantle source for the phoscorite-carbonatite association.
Abstract: In-situ trace element analyses of fluorapatite, calcite, dolomite, olivine, and phlogopite have been undertaken on representative phoscorite and carbonatite rocks of the Palaeoproterozoic Phalaborwa Complex. Textural and compositional characterization reveals uniformity of fluorapatite and calcite among most of the intrusions, and seems to favor a common genetic origin for the phoscorite-carbonatite association. Representing major repositories for rare earth elements (REE), fluorapatite and calcite exhibit tightly correlated light REE (LREE) abundances, suggesting that partitioning of LREE into these rock forming minerals was principally controlled by simple igneous differentiation. However, light rare earth element distribution in apatite and calcite cannot be adequately explained by equilibrium and fractional crystallization and instead favors a complex crystallization history involving mixing of compositionally distinct magma batches, in agreement with previously reported mineral isotope variability that requires open-system behaviour.
Geochimica et Cosmochimica Acta, Vol. 200, pp. 167-185.
Africa, South Africa, Russia
Craton, Peridotite
Abstract: We present Mg and Fe isotopic data for whole rocks and separated minerals (olivine, clinopyroxene, orthopyroxene, garnet, and phlogopite) of garnet peridotites that equilibrated at depths of 134-186 km beneath the Kaapvaal and Siberian cratons. There is no clear difference in ?26Mg and ?56Fe of garnet peridotites from these two cratons. ?26Mg of whole rocks varies from ?0.243‰ to ?0.204‰ with an average of ?0.225 ± 0.037‰ (2?, n = 19), and ?56Fe from ?0.038‰ 0.060 with an average of ?0.003 ± 0.068‰ (2?, n = 19). Both values are indistinguishable from the fertile upper mantle, indicating that there is no significant Mg-Fe isotopic difference between the shallow and deep upper mantle. The garnet peridotites from ancient cratons show ?26Mg similar to komatiites and basalts, further suggesting that there is no obvious Mg isotopic fractionation during different degrees of partial melting of deep mantle peridotites and komatiite formation. The precision of the Mg and Fe isotope data (?±0.05‰ for ?26Mg and ?56Fe, 2?) allows us to distinguish inter-mineral isotopic fractionations. Olivines are in equilibrium with opx in terms of Mg and Fe isotopes. Garnets have the lowest ?26Mg and ?56Fe among the coexisting mantle minerals, suggesting the dominant control of crystal structure on the Mg-Fe isotopic compositions of garnets. Elemental compositions and mineralogy suggest that clinopyroxene and garnet were produced by later metasomatic processes as they are not in chemical equilibrium with olivine or orthopyroxene. This is consistent with the isotopic disequilibrium of Mg and Fe isotopes between orthopyroxene/olivine and garnet/clinopyroxene. Combined with one sample showing slightly heavy ?26Mg and much lighter ?56Fe, these disequilibrium features in the garnet peridotites reveal kinetic isotopic fractionation due to Fe-Mg inter-diffusion during reaction between peridotites and percolating melts in the Kaapvaal craton.
Geochimica et Cosmochimica Acta, in press available 55p.
Africa, South Africa
Deposit - Roberts Victor
Abstract: Heterogeneous, modally banded kyanite-bearing and bimineralic eclogites from the lithospheric mantle, collected at the Roberts Victor Diamond mine (South Africa), show a reaction texture in which kyanite is consumed. Geothermobarometric calculations using measured mineral compositions in Perple_X allowed the construction of a P-T path showing a steep, cool prograde metamorphic gradient of 2 °C/km to reach peak conditions of 5.8 GPa and 890 °C for the kyanite eclogite. The kyanite-out reaction formed bimineralic eclogite and is probably an integral part of the mineralogical evolution of most archetypal bimineralic eclogites at Roberts Victor and potentially elsewhere. The kyanite-out reaction occured at close to peak pressure (5.3 GPa) and was associated with a rise in temperature to 1380 °C. Mass balance calculations show that upon breakdown, the kyanite component is fully accommodated in garnet and omphacite via a reaction system with low water fugacity that required restricted fluid influx from metasomatic sources. The ?18O values of garnets are consistently higher than normal mantle values. Each sample has its characteristic trend of ?18O variance between garnets in the kyanite-bearing sections and those in the bimineralic parts covering a range between 5.1‰ and 6.8‰. No systematic change in O-isotope signature exists across the sample population. Differences in garnet trace element signatures between differing lithologies in the eclogites are significant. Grossular-rich garnets coexisting with kyanite have strong positive Eu-anomalies and low Gd/Yb ratios, while more pyrope-rich garnets in the bimineralic sections have lost their positive Eu-anomaly, have higher Gd/Yb ratios and generally higher heavy rare earth element contents. Garnets in the original kyanite-bearing portions thus reflect the provenance of the rocks as metamorphosed gabbros/troctolites. The kyanite-out reaction was most likely triggered by a heating event in the subcratonic lithosphere. As kyanite contains around 100 ppm of H2O it is suggested that the kyanite-out reaction, once initiated by heating and restricted metasomatic influx, was promoted by the release of water contained in the kyanite. The steep (high-P low-T) prograde P-T path defining rapid compression at low heating rates is atypical for subduction transport of eclogites into the lithospheric mantle. Such a trajectory is best explained in a model where strong lateral compression forces eclogites downward to higher pressures, supporting models of cratonic lithosphere formation by lateral collision and compression.
Abstract: Kimberlitic magmaclasts are discrete ovoid magmatic fragments that formed prior to emplacement from disrupted kimberlite magma. To provide new constraints on the origin and evolution of the kimberlite melts, we document the mineralogy and petrography of a magmaclast recovered from one of the ca. 520 Ma Venetia kimberlites, South Africa. The sample (BI9883) has a sub-spherical shape and consists of a ~ 10 mm diameter central olivine macrocryst, surrounded by porphyritic kimberlite. The kimberlitic material consists of concentrically aligned, altered olivine phenocrysts, set in a crystalline groundmass of calcite, chromite, perovskite, phlogopite, apatite, ilmenite, titanite, sulphides, rutile and magnetite along with abundant alteration phases (i.e. serpentine, talc and secondary calcite). These features are typical of archetypal hypabyssal kimberlites. We examined primary fluid/melt inclusions in chromite, perovskite and apatite containing a diversity of daughter phases. Chromite and perovskite host polycrystalline inclusions containing abundant alkali-carbonates (i.e. enriched in K, Na, Ba, Sr), phosphates, Na-K chlorides, sulphides and equal to lesser quantities of olivine, phlogopite and pleonaste. In contrast, apatite hosts polycrystalline assemblages with abundant alkali-carbonates and Na-K chlorides and lesser amounts of olivine, monticellite and phlogopite. Numerous solid inclusions of shortite (Na2Ca2(CO3)3), Na-Sr-carbonates and apatite occur in groundmass calcite along with fluid inclusions containing daughter crystals of Na-carbonates and Na-chlorides. The primary inclusions in chromite, perovskite and apatite are considered to represent remnants of fluid(s)/melt(s) trapped during crystallisation of the host minerals, whereas the fluid inclusions in calcite are probably secondary in origin. The component proportions of these primary fluid/melt inclusions were estimated in an effort to constrain the composition of the evolving kimberlite melt. These estimates suggest melt evolution from a silicate-carbonate kimberlite melt that became increasingly enriched in carbonates, phosphates, alkalis and chlorides, in response to the fractional crystallisation of constituent minerals (i.e. olivine to apatite). The concentric alignment of crystals around the olivine kernel and ovoid shape of the magmaclast can be ascribed to the low viscosity of the kimberlite melt and rapid rotation whilst in a liquid or partial crystalline state, or to progressive layer-by-layer growth of the magmaclast. Although the mineralogy of our sample is similar to hypabyssal kimberlites worldwide, it differs from hypabyssal kimberlite units in the main Venetia pipes, which contain monticellite-phlogopite rich assemblages and segregationary matrix textures. Therefore magmaclast BI9883 probably originated from a batch of magma distinct from those that produced known hypabyssal units within the Venetia kimberlite cluster.
Abstract: The Mesoproterozoic Pilanesberg Complex, South Africa, is built up by several distinct, ring-shaped intrusions of syenite and peralkaline nepheline syenite. A mildly peralkaline ((Na + K) / Al = 1.04–1.09), medium-to coarse grained nepheline syenite makes up the outermost ring in the southwestern part of the complex (“Matooster type white foyaite”). In this rock, mafic silicate minerals (amphibole, biotite, aegirine) and Ti-bearing minerals (ilmenite, astrophyllite, aenigmatite, lorenzenite, bafertisite, jinshajiangite) are interstitial to feldspar and nepheline, and define a series of mineral assemblages reflecting a change from a miaskitic crystallization regime (with Na-Ca amphibole, titanite and ilmenite) to increasingly agpaitic conditions (with arfvedsonite, aegirine, astrophyllite, aenigmatite, lorenzenite). The main driving force behind the evolution was an increase in peralkalinity of the trapped liquid, mainly by adcumulus growth of alkali feldspar and nepheline, which in the later stages of evolution was combined with increases in oxygen fugacity and water activity. Unlike in most other agpaitic rock complexes, Zr remained compatible in aegirine (and to some extent in amphibole) almost to the end of the process, when a hydrous zirconium silicate mineral (hilairite) crystallized as the only mineral in the rock having essential zirconium. The presence of minerals such as hilairite, bafertisite, jinshajiangite and a Na-REE-Sr rich apatite group mineral (fluorcaphite ?) in the latest assemblages suggests that the last remaining interstitial melt or fluid approached a hyperagpaitic composition. The isolated melt pockets in the Pilanesberg white foyaite follow a pattern of evolution that can be seen as a miniature analogue of the fractional crystallization processes controlling magma evolution in large, alkaline igneous rock complexes.
South African Journal of Geology, Vol. 119, 4, pp. 585-606.
Africa, South Africa
deposit - Lichtenburg Ventersdorp
Abstract: Diamond-bearing gravels of the Lichtenburg-Ventersdorp area of the North West Province are associated with north-south orientated sinuous ‘runs’ that occur almost entirely on a flat erosional surface of the Malmani dolomites (Transvaal Supergroup) at some 1,500 m elevation. East to west, this dolomite plain measures 150 km, and north-south it is on average 40 km wide. This unconformity, which first developed before the Pretoria Group sedimentation over a period of at least 80 Myr, is marked by siliceous breccias (palaeo-karst infill) and conglomerates (reworked breccias). It was exhumed in pre-Karoo and post-Gondwana times. Glacial pavements and remnants of thin Lower Karoo sediments are also found on this polyphase surface. The gravels that make up these ‘runs’ and sinkholes directly or indirectly linked to these runs, are coarse-grained, very poorly-sorted, and are best described as diamictites. The ‘runs’ are narrow, elongated, generally positive ridges that meander across the dolomite surface and are up to 30 km long and between 80 to 300 m wide. They have always been regarded as post-Cretaceous drainage features linked to southward-flowing river systems. Diamonds were discovered in these ‘runs’ and they have produced some 12 million carats. However, no Cainozoic fossils or artefacts have ever been found in almost 90 years of mining. From new field evidence, geomorphological studies, age dating from inclusions in diamond and zircon and clay analyses, it is proposed that these coarse-grained runs represent proximal palaeoeskers of the last deglaciation of the Dwyka continental ice sheet, that are preserved on this ancient ‘palimpsest’ surface. The age of the deposit is constrained by two populations of agate within the diamictites that are linked to two separate volcanic units of the Pretoria Group. In addition, the youngest crustal zircon ages from the gravels are 1 Ba, but mantle zircons from Lichtenburg suggest that these have been derived from Cambrian age kimberlites. Analysis of inclusions in diamond support a Neoproterozoic to Cambrian source for the diamonds, so the absence of diamonds from Mesozoic kimberlites and Cainozoic fossils within the gravels support the conclusion that the runs are of Karoo age.
Abstract: The Pilanesberg Complex (South Africa) is one of the world's largest but least studied alkaline complexes. It consists of trachytes, phonolites, syenites and nepheline syenites (foyaites) and the preservation of the volcanic carapace makes it unique among the larger alkaline complexes. The intrusive history of the Pilanesberg Complex shows similarities to the Greenland Kangerlussuaq Intrusion, and our new whole-rock major and trace element analyses, combined with existing data, show that the complex belongs to the Sr-rich type of evolved alkaline rocks, more similar to the complexes of the Kola Peninsula than Ilímaussaq. Despite the absence of mafic lithologies, comparison with experimental studies shows that the parental magma was most likely an alkali basalt. Significant iron enrichment is caused by an early stage of fractionation involving clinopyroxene and amphibole rather than olivine and plagioclase, reflecting water-rich compositions and intermediate levels of oxygen fugacity. This fractionation trend has led to strong enrichment in Sr and Ba, but only moderate levels of Y and middle to heavy rare earth elements, and minimal Eu-anomaly. Late-stage water-rich fluids caused significant autometasomatism in most units. New U-Pb dating of titanite constrains the age of the Pilanesberg Complex as 1395 + 10/? 11 Ma. Initial 87Sr/86Sr isotope ratios around 0.7028 (?Sr1395 = ? 1) are typical for a moderately depleted mantle source, unlike the local lithospheric mantle. The combination of an enriched trace-element signature and depleted isotopic characteristics is evidence for small degrees of partial melting. Epsilon Sr values are similar to those reported for other alkaline complexes worldwide, emplaced in crust with contrasting geological histories; this likely reflects lithospheric metasomatism shortly before magmatism and minimal crustal contamination.
Abstract: The 2060 Ma old Palabora Carbonatite Complex (PCC), South Africa, comprises diverse REE mineral assemblages formed during different stages and reflects an outstanding instance to understand the evolution of a carbonatite-related REE mineralization from orthomagmatic to late-magmatic stages and their secondary post-magmatic overprint. The 10 rare earth element minerals monazite, REE-F-carbonates (bastnäsite, parisite, synchysite), ancylite, britholite, cordylite, fergusonite, REE-Ti-betafite, and anzaite are texturally described and related to the evolutionary stages of the PCC. The identification of the latter five REE minerals during this study represents their first described occurrences in the PCC as well as in a carbonatite complex in South Africa. The variable REE mineral assemblages reflect a multi-stage origin: (1) fergusonite and REE-Ti-betafite occur as inclusions in primary magnetite. Bastnäsite is enclosed in primary calcite and dolomite. These three REE minerals are interpreted as orthomagmatic crystallization products. (2) The most common REE minerals are monazite replacing primary apatite, and britholite texturally related to the serpentinization of forsterite or the replacement of forsterite by chondrodite. Textural relationships suggest that these two REE-minerals precipitated from internally derived late-magmatic to hydrothermal fluids. Their presence seems to be locally controlled by favorable chemical conditions (e.g., presence of precursor minerals that contributed the necessary anions and/or cations for their formation). (3) Late-stage (post-magmatic) REE minerals include ancylite and cordylite replacing primary magmatic REE-Sr-carbonates, anzaite associated with the dissolution of ilmenite, and secondary REE-F-carbonates. The formation of these post-magmatic REE minerals depends on the local availability of a fluid, whose composition is at least partly controlled by the dissolution of primary minerals (e.g., REE-fluorocarbonates). This multi-stage REE mineralization reflects the interplay of magmatic differentiation, destabilization of early magmatic minerals during subsequent evolutionary stages of the carbonatitic system, and late-stage fluid-induced remobilization and re-/precipitation of precursor REE minerals. Based on our findings, the Palabora Carbonatite Complex experienced at least two successive stages of intense fluid–rock interaction.
Abstract: The petrogenesis of kimberlites is commonly obscured by interaction with hydrothermal fluids, including deuteric (late-magmatic) and/or groundwater components. To provide new constraints on the modification of kimberlite rocks during fluid interaction and the fractionation of kimberlite magmas during crystallisation, we have undertaken a detailed petrographic and geochemical study of a hypabyssal sample (BK) from the Bultfontein kimberlite (Kimberley, South Africa). Sample BK consists of abundant macrocrysts (> 1 mm) and (micro-) phenocrysts of olivine and lesser phlogopite, smaller grains of apatite, serpentinised monticellite, spinel, perovskite, phlogopite and ilmenite in a matrix of calcite, serpentine and dolomite. As in kimberlites worldwide, BK olivine grains consist of cores with variable Mg/Fe ratios, overgrown by rims that host inclusions of groundmass phases (spinel, perovskite, phlogopite) and have constant Mg/Fe, but variable Ni, Mn and Ca concentrations. Primary multiphase inclusions in the outer rims of olivine and in Fe-Ti-rich (‘MUM’) spinel are dominated by dolomite, calcite and alkali carbonates with lesser silicate and oxide minerals. Secondary inclusions in olivine host an assemblage of Na-K carbonates and chlorides. The primary inclusions are interpreted as crystallised alkali-Si-bearing Ca-Mg-rich carbonate melts, whereas secondary inclusions host Na-K-rich C-O-H-Cl fluids. In situ Sr-isotope analyses of groundmass calcite and perovskite reveal similar 87Sr/86Sr ratios to perovskite in the Bultfontein and the other Kimberley kimberlites, i.e. magmatic values. The ?18O composition of the BK bulk carbonate fraction is above the mantle range, whereas the ?13C values are similar to those of mantle-derived magmas. The occurrence of different generations of serpentine and occasional groundmass calcite with high 87Sr/86Sr, and elevated bulk carbonate ?18O values indicate that the kimberlite was overprinted by hydrothermal fluids, which probably included a significant groundwater component. Before this alteration the groundmass included calcite, monticellite, apatite and minor dolomite, phlogopite, spinel, perovskite and ilmenite. Inclusions of groundmass minerals in olivine rims and phlogopite phenocrysts show that olivine and phlogopite also belong to the magmatic assemblage. We therefore suggest that the crystallised kimberlite was produced by an alkali-bearing, phosphorus-rich, silica-dolomitic melt. The alkali-Si-bearing Ca-Mg-rich carbonate compositions of primary melt inclusions in the outer rims of olivine and in spinel grains with evolved compositions (MUM spinel) support formation of these melts after fractionation of abundant olivine, and probably other phases (e.g., ilmenite and chromite). Finally, the similarity between secondary inclusions in kimberlite olivine of this and other worldwide kimberlites and secondary inclusions in minerals of carbonatitic, mafic and felsic magmatic rocks, suggests trapping of residual Na-K-rich C-O-H-Cl fluids after groundmass crystallisation. These residual fluids may have persisted in pore spaces within the largely crystalline BK groundmass and subsequently mixed with larger volumes of external fluids, which triggered serpentine formation and localised carbonate recrystallisation.
Abstract: Magmas forming large igneous provinces (LIP) on continents are generated by extensive melting in the deep crust and underlying mantle and associated with break-up of ancient supercontinents, followed by formation of a new basaltic crust in the mid-oceanic rifts. A lack of the unifying model in understanding the sources of LIP magmatism is justified by lithological and geochemical complexity of erupted magmas on local (e.g. a cross-section) and regional (a single and different LIP) scales. Moreover, the majority of LIP rocks do not fit general criteria for recognizing primary/primitive melts (i.e. < 8 wt% MgO and absence of high-Fo olivine phenocrysts). This study presents the mineralogical (olivine, Cr-spinel, orthopyroxene), geochemical (trace elements and Sr-Nd-Hf-Pb isotopes) and olivine-hosted melt inclusion compositional characteristics of a single primitive (16 wt% MgO), high-Ti (2.5 wt% TiO2) picrite with high-Mg olivine (up to 91 mol% Fo) from the Letaba Formation in the ~ 180 Ma Karoo LIP (south Africa). The olivine compositions (unusually high ?18O (6.17‰), high NiO (0.36–0.56 wt%) and low MnO and CaO (0.12–0.20 and 0.12–0.22 wt%, respectively)) are used to argue for a non-peridotitic mantle source. This is supported by the enrichment of the rock and melts in most incompatible trace elements and depletion in heavy rare earth elements (e.g. high Gd/Yb) that reflects residual garnet in the source of melting. The radiogenic isotopes resemble those of the model enriched mantle (EM-1) and further argue for a long-term enrichment of the source in incompatible trace elements. The enriched high-Ti compositions, strongly fractionated incompatible trace elements, presence of primitive olivine and high-Cr spinel in the Letaba picrites are closely matched by olivine-phyric rocks from the ~ 260 Ma Emeishan (Yongsheng area, SW China) and ~ 250 Ma Siberian (Maimecha-Kotuy region, N Siberia) LIPs. However, many other compositional parameters (e.g. trace element and ?18O compositions of olivine phenocrysts, Fe2 +/Fe3 + in Cr-spinel, Sr-Nd-Hf isotope ratios) only partially overlap or even diverge. We thus imply that parental melts of enriched picritic rocks with forsteritic olivine from three major continental igneous provinces – Karoo, Emeishan and Siberia cannot be assigned to a common mantle source and similar melting conditions. The Karoo picrites also exhibit some mineralogical and geochemical similarities with rocks and glasses in the south Atlantic Ridge and adjacent fracture zones. The geodynamic reconstructions of the continental plate motions since break-up of the Gondwanaland in the Jurassic support the current position of the source of the Karoo magmatism in the southernmost Atlantic. Co-occurrence of modern and recent anomalous rocks with normal mid-ocean ridge basalts in this region can be related to blocks/rafts of the ancient lithosphere, stranded in the ambient upper mantle and occasionally sampled by rifting-related decompressional melting.
Geochemical and petrographical study of megacrysts and mantle xenoliths from Gemsbok Hollow and Gruendorn kimberlites in the Warmbad kimberlite Province, South Africa
Abstract: The widespread occurrence of pyrope garnet in Archean lithospheric mantle remains one of the ‘holy grails’ of mantle petrology. Most garnets found in peridotitic mantle equilibrated with incompatible-trace-element-enriched melts or fluids and are the products of metasomatism. Less common are macroscopic intergrowths of pyrope garnet formed by exsolution from orthopyroxene. Spectacular examples of these are preserved in both mantle xenoliths and large, isolated crystals (megacrysts) from the Kaapvaal craton of southern Africa, and provide direct evidence that some garnet in the sub-continental lithospheric mantle initially formed by isochemical rather than metasomatic processes. The orthopyroxene hosts are enstatites and fully equilibrated with their exsolved phases (low-Cr pyrope garnet ±± Cr-diopside). Significantly, P-TP-T estimates of the post-exsolution orthopyroxenes plot along an unperturbed conductive Kaapvaal craton geotherm and reveal that they were entrained from a large continuous depth interval (85 to 175 km). They therefore represent snapshots of processes operating throughout almost the entire thickness of the sub-cratonic lithospheric mantle. New rare-earth element (REE) analyses show that the exsolved garnets occupy the full spectrum recorded by garnets in mantle peridotites and also diamond inclusions. A key finding is that a few low-temperature exsolved garnets, derived from depths of ~90 km, are more depleted in light REEs than previously observed in any other mantle sample. Importantly, the REE patterns of these strongly LREE-depleted garnets resemble the hypothetical composition proposed for pre-metasomatic garnets that are thought to pre-date major enrichment events in the sub-continental lithospheric mantle, including those associated with diamond formation. The recalculated compositions of pre-exsolution orthopyroxenes have higher Al22O33 and CaO contents than their post-exsolution counterparts and most likely formed as shallow residues of large amounts of adiabatic decompression melting in the spinel-stability field. It is inferred that exsolution of garnet from Kaapvaal orthopyroxenes may have been widespread, and perhaps accompanied cratonization at ~ 2.9 to 2.75 Ga. Such a process would considerably increase the density and stability of the continental lithosphere.
Tracing mantle metasomatism using combined stable (S,O) and radiogenic (Sr, Nd, Hf, Pb) isotope geochemistry: case studies from mantle xenoliths of the Kimberley kimberlites.
Abstract: An oceanic crustal origin is the commonly accepted paradigm for mantle-derived eclogites. However, the significance of the aluminous members of the eclogite suite, containing kyanite and corundum, has long been underrated and their role neglected in genetic models of cratonic evolution. Here, we present a geochemical and petrological study of a suite of kyanite- and corundum-bearing eclogites from the Bellsbank kimberlite, S. Africa, which originate from depths between 150 and 200 km. Although clearly of high-pressure provenance, these rocks had a low-pressure cumulative origin with plagioclase and olivine as major cumulate phases. This is shown by the very pronounced positive Eu anomalies, low REE abundances, and ?18O values lower than the Earth’s mantle. Many chemical features are identical to modern-day troctolitic cumulates including a light REE depletion akin to MORB, but there are also distinguishing features in that the eclogites are richer in Na, Fe, and Ni. Two of the eclogites have a minimum age of ~3.2 Ga, defined by the extremely unradiogenic 87Sr/86Sr (0.7007) in clinopyroxene. Phase equilibria indicate that the parent melts were formed by partial melting below an Archean volcanic center that generated (alkali-)picritic to high-alumina tholeiitic melts from a mantle whose oxygen fugacity was lower than today. Fractional crystallization produced troctolites with immiscible sulfide melt droplets within the mafic crust. Instability of the mafic crust led to deep subduction and re-equilibration at 4–6 GPa. Phase relationships plus the presence of a sample with appreciable modal corundum but no Eu anomaly suggest that kyanite- and corundum-bearing eclogites may also originate as plagioclase-free, higher pressure cumulates of highly aluminous clinopyroxene, spinel, and olivine. This is consistent with the crystallizing phase assemblage from an olivine tholeiitic to picritic magma deeper in the Archean oceanic crust or uppermost mantle. We postulate that the magmatic and subduction processes driving modern plate tectonics already existed in the Meso- to Early Archean.
Geochemistry of the Namaqualand, Busmanland and Warmbad melillitite and kimberlite provinces of South Africa and Namibia: the southern extension of the African kimberlitic megalineament.
Abstract: The Koffiefontein kimberlite is one of the classic locales on the Kaapvaal Craton and best known for being the first locality where very deep diamonds were recovered. Koffiefontein diamonds were last studied in 1980s and, based on major advances in micro-analytical techniques, here we revisit the mine to provide improved inclusion-based geothermobarometry. Currently, ~70 peridotitic diamonds have been studied with ~150 olivine, Cr-rich pyrope garnet, enstatite, and diopside inclusions liberated. So far, the inclusions were analysed (EPMA) for their major element compositions. The peridotitic inclusion suite is dominated by a highly-depleted harzburgitic association: olivine Mg-number ranges between 93 and 95, harzburgitic garnets contain < 3.00 wt % CaO, and 14 % of garnet inclusions are lherzolitic in paragenesis. Conventional mineral exchange geothermobarometry on non-touching inclusion pairs reveals that diamonds with harzburgitic inclusions derive from close to the base of the lithosphere (1143-1283 °C and 55-65 kbar; 12 diamonds) whilst much rarer lherzolitic inclusions last equilibrated in the upper portion of diamond stable lithosphere (983-1158 °C and 47-52 kbar; 5 diamonds). Both associations fall along a 39 mW/m2 reference geotherm (Hasterok and Chapman, 2011), implying a total lithosphere thickness of ~200 km at 90 Ma. To expand our geothermobarometry data beyond rare garnet-opx associations we conducted high-precision trace element analysis of Al and Ca in olivine inclusions via EPMA. Using long count times (300 sec on peak and each background) and a 200 nA beam current, detection limits of 8 ppm for Al and 6 ppm for Ca were achieved. This technique allowed for trace element analysis of olivine inclusions as small as 20 ?m in diameter. Based on these high-precision Al analyses, the updated Al-inolivine thermometer of Bussweiler et al (2017) extrapolated to a 39 mW/m2 geotherm yielded temperatures of 1124-1278 °C (30 diamonds).
Abstract: The petrogenesis of kimberlites is commonly obscured by interaction with hydrothermal fluids, including deuteric (late-magmatic) and/or groundwater components. To provide new constraints on the modification of kimberlite rocks during fluid interaction and the fractionation of kimberlite magmas during crystallisation, we have undertaken a detailed petrographic and geochemical study of a hypabyssal sample (BK) from the Bultfontein kimberlite (Kimberley, South Africa). Sample BK consists of abundant macrocrysts (N1 mm) and (micro-) phenocrysts of olivine and lesser phlogopite, smaller grains of apatite, serpentinised monticellite, spinel, perovskite, phlogopite and ilmenite in a matrix of calcite, serpentine and dolomite. As in kimberlites worldwide, BK olivine grains consist of cores with variable Mg/Fe ratios, overgrown by rims that host inclusions of groundmass phases (spinel, perovskite, phlogopite) and have constant Mg/Fe, but variable Ni, Mn and Ca concentrations. Primary multiphase inclusions in the outer rims of olivine and in Fe-Ti-rich (‘MUM’) spinel are dominated by dolomite, calcite and alkali carbonates with lesser silicate and oxide minerals. Secondary inclusions in olivine host an assemblage of Na-K carbonates and chlorides. The primary inclusions are interpreted as crystallised alkali-Si-bearing Ca-Mg-rich carbonate melts, whereas secondary inclusions host Na-K-rich C-O-H-Cl fluids. In situ Sr-isotope analyses of groundmass calcite and perovskite reveal similar 87Sr/86Sr ratios to perovskite in the Bultfontein and the other Kimberley kimberlites, i.e. magmatic values. The ?18O composition of the BK bulk carbonate fraction is above the mantle range, whereas the ?13C values are similar to those of mantle-derived magmas. The occurrence of different generations of serpentine and occasional groundmass calcite with high 87Sr/86Sr, and elevated bulk carbonate ?18O values indicate that the kimberlite was overprinted by hydrothermal fluids, which probably included a significant groundwater component. Before this alteration the groundmass included calcite, monticellite, apatite and minor dolomite, phlogopite, spinel, perovskite and ilmenite. Inclusions of groundmass minerals in olivine rims and phlogopite phenocrysts show that olivine and phlogopite also belong to the magmatic assemblage. We therefore suggest that the crystallised kimberlite was produced by an alkali-bearing, phosphorus-rich, silica-dolomitic melt. The alkali-Si-bearing Ca-Mg-rich carbonate compositions of primary melt inclusions in the outer rims of olivine and in spinel grains with evolved compositions (MUM spinel) support formation of these melts after fractionation of abundant olivine, and probably other phases (e.g., ilmenite and chromite). Finally, the similarity between secondary inclusions in kimberlite olivine of this and other worldwide kimberlites and secondary inclusions in minerals of carbonatitic, mafic and felsic magmatic rocks, suggests trapping of residual Na-K-rich C-O-H-Cl fluids after groundmass crystallisation. These residual fluids may have persisted in pore spaces within the largely crystalline BK groundmass and subsequently mixed with larger volumes of external fluids, which triggered serpentine formation and localised carbonate recrystallisation.
Abstract: The concept of vertical pit mining has developed as an alternative mining method for the exploitation from surface of small, vertical or near vertical, massive orebodies to depths of approximately 100 m where ore extraction can become uneconomical due to high stripping ratios. Support of the sidewalls is ensured with systematic anchoring depending on the condition of the insitu rock mass together with the installation of mesh and shotcrete in order to prevent small-scale ravelling and spalling which, with the pit at depth, can prove hazardous to operations at the base of the pit. Hoisting of the ore is carried out either by a vertical A Frame hoist at the crest of the pit, which requires tramming of ore at the base of the pit to the hoist. Alternatively, a Blondin Cableway system, which allows for loading of kibbles at any location within the pit, negating the need for a tram to the hoist located on the side of the pit, can be utilised. For various reasons the technique has been successfully applied to the mining of a chrome deposit in Zimbabwe to a depth of 95m and a kimberlite pit in West Africa where the pit was terminated at a depth of 85m due to a sidewall failure. Feasibility studies for two further vertical pits were conducted for orebodies in South Africa and Australia, kimberlite and nickel respectively, but due to economic considerations, have not been mined.
The Archean sedimentary sulfur recycling under the Kaapvaal craton revisited from 4S- isotopic compositions in sulfide inclusions in diamonds from Kimberley Pool.
Abstract: Fibrous diamond growth zones can contain abundant high density fluid inclusions (HDFs) and these provide the most direct information on the source and composition of diamond-forming fluids. Four different fluid end-members have been defined; silicic, low-Mg carbonatitic, high-Mg carbonatitic, and saline. Continuous arrays exist between the silicic and low-Mg carbonatitic end-member and between the saline and high-Mg carbonatitic end-member. Different processes have been proposed to explain the two major element compositional arrays, but the origin of and relation between the various fluid end-members is still uncertain. In this study we provide new constraints on the evolution and origin of these diamond-forming fluids by combining noble gas systematics with ?13C, N concentrations, and fluid inclusion compositions.
Geochemical Perspectives Letters, Vol. 4, pp. 1-6.
Africa, South Africa, Zimbabwe
metasomatism, geochronology
Abstract: Metasomatism, the chemical alteration of rocks by a variety of melts and fluids, has formed a key concept in studies of the Earth’s mantle for decades. Metasomatic effects are often inferred to be far-reaching and yet the evidence for their occurrence is usually based upon individual hand specimens or suites of rocks that display considerable heterogeneity. In rare cases, however, we are offered insights into larger-scale chemical modifications that occur in the mantle. Here we utilise the Lu–Hf systematics of zircon megacrysts erupted in kimberlite magmas to discern two temporally and compositionally discrete metasomatic events in the mantle beneath southern Africa, each having an influence extending over an area exceeding one million km2. These data provide unambiguous evidence for metasomatic processes operating at continental scales and seemingly unperturbed by the age and composition of the local lithospheric mantle. The most recent of these events may be associated with the major Jurassic-Karoo magmatism in southern Africa.
Earth and Planetary Science Letters, Vol. 474, pp. 283-295.
Africa, South Africa
deposit - Lace
Abstract: Reconstructing the redox state of the mantle is critical in discussing the evolution of atmospheric composition through time. Kimberlite-borne mantle eclogite xenoliths, commonly interpreted as representing former oceanic crust, may record the chemical and physical state of Archaean and Proterozoic convecting mantle sources that generated their magmatic protoliths. However, their message is generally obscured by a range of primary (igneous differentiation) and secondary processes (seawater alteration, metamorphism, metasomatism). Here, we report the Fe3+/?Fe ratio and ?18 O in garnet from in a suite of well-characterised mantle eclogite and pyroxenite xenoliths hosted in the Lace kimberlite (Kaapvaal craton), which originated as ca. 3 Ga-old ocean floor. Fe3+/?Fe in garnet (0.01 to 0.063, median 0.02; n = 16) shows a negative correlation with jadeite content in clinopyroxene, suggesting increased partitioning of Fe3+ into clinopyroxene in the presence of monovalent cations with which it can form coupled substitutions. Jadeite-corrected Fe3+/?Fe in garnet shows a broad negative trend with Eu*, consistent with incompatible behaviour of Fe3+ during olivine-plagioclase accumulation in the protoliths. This trend is partially obscured by increasing Fe3+ partitioning into garnet along a conductive cratonic geotherm. In contrast, NMORB-normalised Nd/Yb - a proxy of partial melt loss from subducting oceanic crust (<1) and metasomatism by LREE-enriched liquids (>1) - shows no obvious correlation with Fe3+/?Fe, nor does garnet ?18OVSMOW (5.14 to 6.21‰) point to significant seawater alteration. Median bulk-rock Fe3+/?Fe is roughly estimated at 0.025. This observation agrees with V/Sc systematics, which collectively point to a reduced Archaean convecting mantle source to the igneous protoliths of these eclogites compared to the modern MORB source. Oxygen fugacites (fO2) relative to the fayalite-magnetite-quartz buffer (FMQ) range from ?log ? fO2 = FMQ-1.3 to FMQ-4.6. At those reducing conditions, the solubility of carbon in the fluids released by dehydration is higher than in fluids closer to FMQ. The implication is that Archean processes of C transport and deposition would have differed from those known in modern-style subduction zones, and diamond would have formed from methane-rich fluids. In addition, such reducing material could drive redox melting or freezing upon deep recycling and migration of CH4-bearing fluids into the ambient mantle.
Journal of Structural Geology, Vol. 86, pp. 47-61.
Africa, South Africa
deposit - Venetia
Abstract: The Beit Bridge Complex of the Central Zone (CZ) of the Limpopo Belt hosts the 519 ± 6 Ma Venetia kimberlite diatremes. Deformed shelf- or platform-type supracrustal sequences include the Mount Dowe, Malala Drift and Gumbu Groups, comprising quartzofeldspathic units, biotite-bearing gneiss, quartzite, metapelite, metacalcsilicate and ortho- and para-amphibolite. Previous studies define tectonometamorphic events at 3.3-3.1 Ga, 2.7-2.5 Ga and 2.04 Ga. Detailed structural mapping over 10 years highlights four deformation events at Venetia. Rules-based implicit 3D modelling in Leapfrog Geo™ provides an unprecedented insight into CZ ductile deformation and sheath folding. D1 juxtaposed gneisses against metasediments. D2 produced a pervasive axial planar foliation (S2) to isoclinal F2 folds. Sheared lithological contacts and S2 were refolded into regional, open, predominantly southward-verging, E-W trending F3 folds. Intrusion of a hornblendite protolith occurred at high angles to incipient S2. Constrictional-prolate D4 shows moderately NE-plunging azimuths defined by elongated hornblendite lenses, andalusite crystals in metapelite, crenulations in fuchsitic quartzite and sheath folding. D4 overlaps with a: 1) 2.03-2.01 Ga regional M3 metamorphic overprint; b) transpressional deformation at 2.2-1.9 Ga and c) 2.03 Ga transpressional, dextral shearing and thrusting around the CZ and d) formation of the Avoca, Bellavue and Baklykraal sheath folds and parallel lineations.
Abstract: The nitrogen isotopic composition of mantle samples lie between -15 to -5 ‰ and, is different from subducted sediments that varies between +6 to +15 ‰. As a result, N can be an excellent tracer of a subducted component [e.g. 1]. We have studied N from Indian carbonatites of adjacent locations in Hogenakal (2700 Ma) and Sevattur (770 Ma) with established mantle origin. We have also studied two diamonds representative of the Witwatersrand basin (2900–2700 Ma) and Jagersfontein (1100-1700 Ma) belonging to the Kapvaal supergroup. Both India and the Kapvaal craton formed part of a supercontinent that persisted as coherent units until the breakup of Pangea. Comparing the N in these diamonds with the carbonatites will put constraints on differences in their sources and the role of subduction in their generation. The nitrogen isotopic composition of the carbonatites are comparable ranging between -3 to +13 ‰, although value as low as -22 ‰ is observed from an apatite from Hogenakal. The N contents vary from 130 to 6000 ppb. Of the diamonds, Jagersfontein have ?15N of +2.3 and +9.3 ‰, while those from the Witwatersrand basin are –2.3 and 0 ‰. Their nitrogen lie between 500-900 ppm. These results have important implications for their formation and sources.
Abstract: The Pilanesberg Alkaline Complex (South Africa) consists of a partially eroded phonolitic-trachytic package of lavas and tuffs, intruded by consanguinous syenites and nepheline syenites (foyaites). The latter have been divided in several units, based on their colour and mineralogy. Most of the foyaitic units are sodic in composition, but whole rock analyses show that some samples are more potassic, with Na2O/K2O<0.8. This observation, together with old reports of leucite-bearing lavas [1], could suggest the existence of a second, potassic magmatic lineage. To investigate whether the observed potassium-enrichment is a primary feature, or the result of deuteric alteration, the mineralogical distinction between sodic and potassic samples was investigated. The mineralogy of the sodic samples is dominated by nepheline, alkali-feldspar and aegirine, ± titanite, amphibole, biotite, and late agpaitic phases [2]. Within the potassic samples, the main primary ferromagnesian mineral is biotite, which shows conspicuous zoning in thin section; nepheline has been extensively replaced by sodalite and cancrinite, but alkali-feldspar appears relatively unaltered. No agpaitic minerals were observed. U-Pb isotope systematics of titanite are similar for sodic and potassic samples in terms of the age (ca. 1.4 Ga) and composion of common Pb; Ar-Ar dating of biotite also gives ca. 1.4 Ga, showing that biotite is a primary magmatic phase. Compositions of the biotite in sodic and potassic samples are similar, with the sodic samples having slightly higher Fe# (independent of whole rock Fe#), higher Na, but lower (Na+K) and Ba. Zoning in biotite from potassic samples is related to a decrease in Mg, Ti and F in the rim of the crystals. Despite the primary character of the biotite, the question whether the potassic samples reflect a combination of alteration and perhaps minor crustal contamination, or a separate mag
Abstract: The widespread occurrence of pyrope garnet in Archean lithospheric mantle remains one of the ‘holy grails’ of mantle petrology. Most garnets found in peridotitic mantle equilibrated with incompatible-trace-element-enriched melts or fluids and are the products of metasomatism. Less common are macroscopic intergrowths of pyrope garnet formed by exsolution from orthopyroxene. Spectacular examples of these are preserved in both mantle xenoliths and large, isolated crystals (megacrysts) from the Kaapvaal craton of southern Africa, and provide direct evidence that some garnet in the sub-continental lithospheric mantle formed initially by isochemical rather than metasomatic processes. The orthopyroxene hosts are enstatites and fully equilibrated with their exsolved phases (low-Cr pyrope garnet?±?Cr-diopside). Significantly, P-T estimates of the post-exsolution orthopyroxenes plot along an unperturbed conductive Kaapvaal craton geotherm and reveal that they were entrained from a large continuous depth interval (85 to 175?km). They therefore represent snapshots of processes operating throughout almost the entire thickness of the sub-cratonic lithospheric mantle. New rare-earth element (REE) analyses show that the exsolved garnets occupy the full spectrum recorded by garnets in mantle peridotites and also diamond inclusions. A key finding is that a few low-temperature exsolved garnets, derived from depths of ?90?km, are more depleted in light rare-earth elements (LREEs) than previously observed in any other mantle sample. Importantly, the REE patterns of these strongly LREE-depleted garnets resemble the hypothetical composition proposed for pre-metasomatic garnets that are thought to pre-date major enrichment events in the sub-continental lithospheric mantle, including those associated with diamond formation. The recalculated compositions of pre-exsolution orthopyroxenes have higher Al2O3 and CaO contents than their post-exsolution counterparts and most probably formed as shallow residues of large amounts of adiabatic decompression melting in the spinel-stability field. It is inferred that exsolution of garnet from Kaapvaal orthopyroxenes may have been widespread, and perhaps accompanied cratonization at ?2.9 to 2.75 Ga. Such a process would considerably increase the density and stability of the continental lithosphere.
Abstract: The Palabora Carbonatite Complex (PCC) in South Africa intruded at 2060 Ma into Archean basement. The tripartite pipe-like intrusion is represented by a northern and southern pyroxenite and the central Loolekop pipe. Carbonatites and phoscorites of the Loolekop pipe experienced at least 4 stages of mineralization, recrystallization and redistibution reflected by an (1) orthomagmatic, (2) late-magmatic, (3) sulphide and (4) post-magmatic phase (Giebel et al., 2017). These four stages exhibit considerable variability of REE mineralization and especially stages 2 and 4 show intense fluid-rock interaction textures. We present microtextural and compositional data on apatite and phlogopite along a 2 km depth profile through the Loolekop pipe and investigate how these data reflect fluidmineral interaction with depth during stage (2). A special focus lies on understanding the behaviour, sources and sinks of REE elements. While fluid-apatite interaction causes a dissolution of apatite coupled with a precipitation of monazite at apatite rims, the fluid-phlogopite interaction induces a chloritization of phlogopite and an occasional formation of britholite along strongly dissolved phlogopite rims. We suspect that REE are transported into the system by this late-magmatic fluid rather than being released by the dissolution of orthomagmatic REE-bearing minerals. Combining these observations with fluid inclusion textures and microthermometry, we will investigate the nature and composition of the involved fluids and will try to model REE mineralisation processes during late-magmatic fluidmineral ineraction
Abstract: Metasomatised regions of Earth’s sub-continental lithospheric mantle potentially represent a large volatile reservoir. Nevertheless, the mechanisms involved in the storage and upward transport of volatiles such as C and S, from the convecting mantle and/or subducting slabs, are poorly understood. We have carried out a systematic microanalytical study of a suite of sulfide-rich mantle peridotites from the Bultfontein diamond mine, Kimberley. EDS mapping of large (>2mm), interstitial base metal sulfides in the Bultfontein xenoliths has identified distinct Ni-rich regions (pentlandite). The Ni-rich sulfides are adjacent to olivine with Ni poor rims (<0.2 wt% NiO). Diffusion profiles between the protolith olivines and adjacent sulfides are used to estimate the timing of the S-rich metasomatic event. The presence of large unequilibrated olivine indicates that Nisulfides were introduced immediately prior to kimberlite emplacement. The calculated composition of melt in equilibrium with metasomatic clinopyroxenes in the Bultfontein sulphide-bearing peridotites shows a strong correlation to high-density carbonatitic fluids trapped in diamonds. This association is extended by the wealth of metasomatic sulfides in the Bultfontein xenoliths. Moreover, Ni-rich sulfides (~25 wt%) are the most common mineral inclusion in peridotitic diamonds, implying that diamonds crystallise from a S-saturated fluid. Many studies attribute the metasomatism at Bultfontein to silicate melts associated with the kimberlite, but we explore the possibility of metasomatism by reactive percolation of a volatile-rich agent with carbonatitic affinity. The S-rich nature of the metasomatism and the correlation with diamond high-density fluids has great implications for the transport of volatiles from the deep mantle to shallow regions of the craton.
Abstract: Polycrystalline diamond aggregates (diamondites) are produced by rapid crystal nucleation caused by extreme carbon supersaturation in mantle fluids. They may form episodically and under variable chemical conditions, providing snapshots of diamond formation in the Earth’s mantle. Diamondites, thus, represent an extreme end member of diamond formation mechanisms, while forming via the same processes and ingredients as the gem-sized diamonds. We present results on a large suite of diamondites from the Venetia mine (South Africa), comprising a complete characterisation of the diamonds and their silicate inclusions and intergrowths. The highlighted characteristic of this sample suite is its heterogeneity in all aspects, from affiliated silicate to diamond composition and texture of the diamond aggregates. The diamond grains in the samples are intergrown with silicates (garnets, clinopyroxenes, phlogopites) comprising a websteritic-eclogitic and a peridotiticpyroxenitic suite of minerals. Diamonds, regardless of their affiliation based on their silicate phases, overlap in carbon and nitrogen composition and have ?13C values between -28 and -8 ‰, ?15N values of 0.8 to 16.3 ‰ and nitrogen contents of 4 to 2329 ppm. The entire range of carbon and nitrogen variability of the suite is also reflected in some individual samples. Cathodoluminescence imaging visualizes different zones in the samples that can be interpreted as different growth events with differing nitrogen contents and ?15N decoupled from ?13C values, in line with the variability off nitrogen aggregation states. Electron backscatter diffraction analyses identify an original texture of randomly intergrown diamond grains that is partly changed by deformation and newly grown smaller diamond grains. The large overall variability suggesting episodic formation of diamondite with nitrogen from crustal sources.
South African Institute of Mining and Metallurgy, Vol. 116, 8, pp. 745-752.
Africa, South Africa
deposit - Cullinan
Abstract: In 2012, Cullinan Diamond Mine began an expansion programme with the shaft deepening and development of access to the C-Cut 1 block at approximately 839 m below surface. The expansion programme is funded by a combination of bank loans and retained operating profit generated by the mine. Continuous production during deepening of the No. 1 Shaft, which is the rock hoisting shaft, was therefore critical for sustainability and efficiency as well as overall funding of the project. The deepening method, support design and verification, as well as learning outcomes pertaining to the extension of the No. 1 Shaft underneath the existing operating shaft are summarized, with emphasis on the importance of gaining some understanding of the shaft's host rock mass.
Abstract: Diamond inclusions are the only samples from the mantle transition zone (410-660 km) and the lower mantle. Majoritic garnet is a rare inclusion, limited to pressures of ~8-20 Gpa with Si content being indicative of depth of re-equilibration. These garnet inclusions can therefore provide information on properties of the transition zone such as oxidation state. In this study, we used Synchrotron Mössbauer Source (SMS) to determine the ferric-ferrous ratios of 13 small (30 to 100 micrometers diameter) majoritic inclusions in diamonds from Jagersfontein. The studied inclusions have pyroxenitic affinities [1], with compositions intermediate between typical peridotite and eclogite. They contain 4.62-11.2 wt% CaO, 0.03-0.34 wt% Cr2O3 and Mg# of 0.65-0.81. Minimum pressures for their equilibration using Beyer and Frost [2] barometer are between 8 and 18 GPa with at least 4 of these inclusions being formed in the transition zone. The Fe3+/Fetotal ratios in the garnets increase from 0.08±0.01 to 0.30±0.03 with increasing pressure. These values define a clear extension of the trend apparent in the data from peridotite xenoliths crystallised at lower pressures. Thermodynamic calculations suggest that these high ferric contents correspond to oxygen fugacities above the FeFeO (IW) buffer, which means that the high Fe3+ contents were not generated by disproportionation of Fe2+ to Fe3+ and Fe0 . It is more likely that carbonate was the oxidising agent responsible for generating the high Fe3+ of these garnets.
South African Institute of Mining and Metallurgy, Vol. 116, 4, pp. 343-350.
Africa, South Africa
deposit - Cullinan
Abstract: Near-infrared (NIR) spectroscopy sorting technology is incorporated in an automated optical mineral sorter that can discriminate between materials using the differences in characteristics when exposed to near-infrared radiation. During September 2014 to April 2015, a pilot plant that utilized NIR technology to discriminate between kimberlite and waste materials was commissioned to determine the viability of including this technology in the diamond winning process flow sheet at Cullinan Diamond Mine. The plant was used to minimize the waste content in the size fraction -70+35 mm that reports to the crushing section and then to the dense media separation process. This paper describes the initial test work, conducted at Mintek, that led to the decision to conduct a pilot-scale study. The mineralogical characterization of the feed and product streams to establish the sorting criteria and the operational data obtained during the pilot plant campaign are described. The results indicated a good possibility of discriminating between the kimberlite and waste material using NIR technology. However, the consistency of discrimination was not good enough to avoid the risk of potential diamond loss. Furthermore, a lower than expected availability of the machine reduced the throughput capabilities.
Abstract: Heterogeneous, modally banded kyanite-bearing and bimineralic eclogites from the lithospheric mantle, collected at the Roberts Victor Diamond mine (South Africa), show a reaction texture in which kyanite is consumed. Geothermobarometric calculations using measured mineral compositions in Perple_X allowed the construction of a P-T path showing a steep, cool prograde metamorphic gradient of 2 °C/km to reach peak conditions of 5.8 GPa and 890 °C for the kyanite eclogite. The kyanite-out reaction formed bimineralic eclogite and is probably an integral part of the mineralogical evolution of most archetypal bimineralic eclogites at Roberts Victor and potentially elsewhere. The kyanite-out reaction occured at close to peak pressure (5.3 GPa) and was associated with a rise in temperature to 1380 °C. Mass balance calculations show that upon breakdown, the kyanite component is fully accommodated in garnet and omphacite via a reaction system with low water fugacity that required restricted fluid influx from metasomatic sources. The ?18O values of garnets are consistently higher than normal mantle values. Each sample has its characteristic trend of ?18O variance between garnets in the kyanite-bearing sections and those in the bimineralic parts covering a range between 5.1‰ and 6.8‰. No systematic change in O-isotope signature exists across the sample population. Differences in garnet trace element signatures between differing lithologies in the eclogites are significant. Grossular-rich garnets coexisting with kyanite have strong positive Eu-anomalies and low Gd/Yb ratios, while more pyrope-rich garnets in the bimineralic sections have lost their positive Eu-anomaly, have higher Gd/Yb ratios and generally higher heavy rare earth element contents. Garnets in the original kyanite-bearing portions thus reflect the provenance of the rocks as metamorphosed gabbros/troctolites. The kyanite-out reaction was most likely triggered by a heating event in the subcratonic lithosphere. As kyanite contains around 100 ppm of H2O it is suggested that the kyanite-out reaction, once initiated by heating and restricted metasomatic influx, was promoted by the release of water contained in the kyanite. The steep (high-P low-T) prograde P-T path defining rapid compression at low heating rates is atypical for subduction transport of eclogites into the lithospheric mantle. Such a trajectory is best explained in a model where strong lateral compression forces eclogites downward to higher pressures, supporting models of cratonic lithosphere formation by lateral collision and compression.
Geochimica et Cosmochimica Acta, in press available, 22p.
Africa, South Africa
deposit - Venetia
Abstract: Re-Os and platinum group element analyses are reported for peridotite xenoliths from the 533 Ma Venetia kimberlite cluster situated in the Limpopo Mobile Belt, the Neoarchaean collision zone between the Kaapvaal and Zimbabwe Cratons. The Venetian xenoliths provide a rare opportunity to examine the state of the cratonic lithosphere prior to major regional metasomatic disturbance of Re-Os systematics throughout the Phanerozoic. The 32 studied xenoliths record Si-enrichment that is characteristic of the Kaapvaal lithospheric mantle and can be subdivided into five groups based on Re-Os analyses. The most pristine group I samples (n = 13) display an approximately isochronous relationship and fall on a 3.28 ± 0.17 Ga (95 % conf. int.) reference line that is based on their mean TMA age. This age overlaps with the formation age of the Limpopo crust at 3.35–3.28 Ga. The group I samples derive from ?50 to ?170 km depth, suggesting coeval melt depletion of the majority of the Venetia lithospheric mantle column. Group II and III samples have elevated Re/Os due to Re addition during kimberlite magmatism. Group II has otherwise undergone a similar evolution as the group I samples with overlapping 187Os/188Os at eruption age: 187Os/188OsEA, while group III samples have low Os concentrations, unradiogenic 187Os/188OsEA and were effectively Re-free prior to kimberlite magmatism. The other sample groups (IV and V) have disturbed Re-Os systematics and provide no reliable age information. A strong positive correlation is recorded between Os and Re concentrations for group I samples, which is extended to groups II and III after correction for kimberlite addition. This positive correlation precludes a single stage melt depletion history and indicates coupled remobilisation of Re and Os. The combination of Re-Os mobility, preservation of the isochronous relationship, correlation of 187Os/188Os with degree of melt depletion and lack of radiogenic Os addition puts tight constraints on the formation and subsequent evolution of Venetia lithosphere. First, melt depletion and remobilisation of Re and Os must have occurred within error of the 3.28 Ga mean TMA age. Second, the refractory peridotites contain significant Re despite recording >40 % melt extraction. Third, assuming that Si-enrichment and Re-Os mobility in the Venetia lithospheric mantle were linked, this process must have occurred within ?100 Myr of initial melt depletion in order to preserve the isochronous relationship. Based on the regional geological evolution, we propose a rapid recycling model with initial melt depletion at ?3.35 Ga to form a tholeiitic mafic crust that is recycled at ?3.28 Ga, resulting in the intrusion of a TTG suite and Si-enrichment of the lithospheric mantle. The non-zero primary Re contents of the Venetia xenoliths imply that TRD model ages significantly underestimate the true depletion age even for highly depleted peridotites. The overlap of the ?2.6 Ga TRD ages with the time of the Kaapvaal-Limpopo collision is purely fortuitous and has no geological significance. Hence, this study underlines the importance of scrutiny if age information is to be derived from whole rock Re-Os analyses.
Abstract: Precise dating of diamond growth is required to understand the interior workings of the early Earth and the deep carbon cycle. Here we report Sm-Nd isotope data from 26 individual garnet inclusions from 26 harzburgitic diamonds from Venetia, South Africa. Garnet inclusions and host diamonds comprise two compositional suites formed under markedly different conditions and define two isochrons, one Archaean (2.95?Ga) and one Proterozoic (1.15?Ga). The Archaean diamond suite formed from relatively cool fluid-dominated metasomatism during rifting of the southern shelf of the Zimbabwe Craton. The 1.8 billion years younger Proterozoic diamond suite formed by melt-dominated metasomatism related to the 1.1?Ga Umkondo Large Igneous Province. The results demonstrate that resolving the time of diamond growth events requires dating of individual inclusions, and that there was a major change in the magmatic processes responsible for harzburgitic diamond formation beneath Venetia from the Archaean to the Proterozoic.
Van der Meer, Q., Klaver, M., Reisberg, L., Riches, A. J.V., Davies, G.R.
Preservation of an Archean whole rock Re-Os isochron for the Venetia lithospheric mantle: evidence for rapid crustal recycling and lithosphere stabilization at 3.3 Ga.
Geochimica et Cosmochimica Acta, Vol. 216, pp. 242-263.
South African Journal of Geology, Vol. 120, 1, pp. 1-20.
Africa, South Africa
deposit - Jagersfontein
Abstract: Our earlier studies continued in a diligent search for rare ultradeep xenoliths in the kimberlite diatreme at Jagersfontein. The search has met with moderate success insofar as 20 majorite-bearing (decomposed to *gt + lamellar px) xenoliths are identified. Discrete gts (1 to 2 cm), gt-rich layers (2 to 3 cm) in lherzolites, and rare megacrystic gts (>3 cm) from xenoliths characterize the ultradeep suite. Pyroxene lamellae are crystallographically controlled along {111} gt planes, but px may also be prismatic, lensoidal, coarsely graphic, or annular to gt; jigsaw, rather than 120° dihedral textures, are typical. Gt ranges from Pyr68-74 mole% and CaO - Cr2O3 relations, with two exceptions, are distinctly lherzolitic. Cpx37-46 = Wo mole%, Jd 3-19 mole%, with 0.4 to 2.4 wt% Cr2O3; opx = 92 to 95 mole% en, and ol averages 92.5 mole% with maximum wt% 0.1 CaO, 0.4 NiO, and 0.1 Cr2 O3. A new class of 10 ultradeep xenoliths has lamellar spinel (Cr/Cr + Al = 0.74; Mg/Mg + Fe = 0.58) in addition to cpx with gt >3wt% Cr2O3 (c.f. 0.5 to 1.5 for sp-free types). Five samples are texturally linked but are compositional outliers to the central body of data: two are sp hosts (Cr# 0.69, Mg# 0.76) and (Cr# 0.74, Mg# 0.57) to gt (Pyr72) + cpx (Jd14); one is a gt megacryst (Pyr80) with sp (Cr# 57, Mg# 69); and the remaining two are unusually rich in chromium with gt = 7.3 to 8.2 wt% Cr2O3, rimmed by cpx (2.3 to 3.3 wt% Cr2O3). In addition, there are 17 xenoliths with compositional affinities to the ultradeep suite but lacking the texturally diagnostic lamellar intergrowths of cpx in gt are possibly completely equilibrated to gt + irregular cpx. Results from the new collection substantiate our earlier conclusions that the mantle was sampled by the Jagersfontein kimberlite from the lower lithosphere (250 to 350 km) and the transition zone (435 km) with diagnostic high P-T majorite in lherzolite that decomposed to gt + px at one or more interruptive stations (e.g. lithosphere-asthenosphere boundary), and at one or another time, en route to the surface. Homogeneous majorite occurs as diamond inclusions at Jagersfontein but these are eclogitic, leading to the proposition that the source region in the asthenosphere was an unassimilated mixture of lherzolite and eclogite in the Mid-Cretaceous at the time of kimberlite sampling. Important questions arise: Is majorite primordial; did majorite form exclusively from the transition of pyroxene; or did subsequent dissolution into coexisting garnet take place? Why has majorite not been identified in eclogite, nor diamonds of lherzolitic affinity? Does the formation of majorite and the crystallization of encapsulating diamond imply distinct high P-T events?
Abstract: A series of terraces flanking the Lower Orange River in the study area were deposited after ca. 90% of the incision had occurred, thus only the late stage incision/depositional history of this margin is able to be addressed here. Two principal suites of river terraces are distinguished by their palaeo-courses, bedrock strath levels, overall geometry and clast assemblages: an older, higher lying Proto suite and a younger Meso suite. The Proto suite represents a long, post-Eocene, through the Oligocene into the Early Miocene, phase of incision, followed by a prolonged period of aggradation where up to 90 m of fluvial, diamondiferous deposits accumulated during the Early-Middle Miocene. The Meso suite of deposits represents shorter phrases of incision and aggradation in the Pilo-Pleistocene. The Proto and Meso deposits were built in response to both base level rise and increased supply of material from tributaries draining the Great Escarpment locally, with clast assemblage and downstream fining data indicating the latter to be the more important variable. River incision into bedrock is a topic of great interest to fluvial geomorphologists, although most data are derived from active tectonic settings. The incision of a large river into a plateau surface is relatively rare, the best known example being the Colorado River in the young (6 Ma) Grand Canyon. The Orange River in the study area represents a long-lived example of this setting, with the present day dissected topography having evolved from more confined canyon-like walls following the early incision of the Orange River in the Early Tertiary. Although a long-lived incision, the modern channel is not graded in the study area, and is actively incising. The world-wide dataset of incision rates in modern rivers indicates that the Orange River could have completed its entire incision within less than a million years. The continued downcutting of this river so long after the initial incision event is indicative of the roles of intermittent, ongoing epeirogenesis and/or eustatic influences (both of which cannot be proven at this stage), tributary input from the plateau rim (Great Escarpment) or merely the long tag time involved in landscape adjustment following incision into a plateau surface.
Earth and Planetary Science Letters, Vol. 481, pp. 143-153.
Africa, South Africa
deposit - Wesselton
Abstract: Rare garnet crystals from a peridotite xenolith from the Wesselton kimberlite, South Africa, have distinct zones related to two separate episodes of mantle metasomatism. The garnet cores were firstly depleted through melt extraction, then equilibrated during metasomatism by a potentially diamond-forming carbonate-bearing or proto-kimberlitic fluid at 1100-1300?°C and 4.5-5.5 GPa. The garnet rim chemistry, in contrast, is consistent with later overgrowth in equilibrium with a kimberlite at around and . This suggests that the rock was physically moved upwards by up to tens of kilometres between the two metasomatic episodes. Preserved high Ca, Al and Cr contents in orthopyroxenes suggest this uplift was tectonic, rather than magmatic. Diffusion profiles were measured over the transitions between garnet cores and rims using electron microprobe (Mg, Ca, Fe for modelling, plus Cr, Mn, Ti, Na, Al) and nano Secondary Ion Mass Spectrometry (NanoSIMS; 89Y, along with 23Na, Ca, Cr, Fe, Mn and Ti) analyses. The short profile lengths (generally <10 ?m) and low Y concentrations (0.2-60 ppm) make the NanoSIMS approach preferable. Diffusion profiles at the interface between the zones yield constraints on the timescale between the second metasomatic event and eruption of the kimberlite magma that brought the xenolith to the surface. The time taken to form the diffusion profiles is on the order of 25 days to 400 yr, primarily based on modelling of Y diffusion along with Ca, Fe and Mg (multicomponent diffusion) profiles. These timescales are too long to be produced by the interaction of the mantle xenolith with the host kimberlite magma during a single-stage ascent to the crust (hours to days). The samples offer a rare opportunity to study metasomatic processes associated with failed eruption attempts in the cratonic lithosphere.
Geochemistry, Geophysics, Geosystems, Vol. 18, 10, pp. 3556-3575.
Africa, South Africa
geodynamics
Abstract: The deep mantle African Superswell is considered to contribute to the topographic uplift of the Southern African Plateau, but dynamic support estimates vary wildly depending on the approach and data used. One reason for these large disparities is that the role of lithospheric structure, key in modulating deep dynamic contributions to elevation, is commonly ignored or oversimplified in convection studies. We use multiple high-quality geophysical data coupled with xenolith-based geochemical constraints to compute the isostatic lithospheric contribution to the elevation of the Plateau, facilitating isolation of the current dynamic component from the total observed elevation. We employ a multiobservable stochastic algorithm to invert geoid anomaly, surface-wave dispersion data, magnetotelluric data, and surface heat flow to predict elevation in a fully thermodynamically and internally-consistent manner. We find that a compositionally layered 230?±?7 km thick lithosphere is required to simultaneously fit all four data types, in agreement with abundant independent xenolith evidence. Our stochastic modeling indicates a lithospheric contribution to elevation of the order of 670 m, which implies dynamic support arising from the convecting sublithospheric mantle of ?650 m. Our results have important implications for the understanding of lithospheric-deep mantle feedback mechanisms and for calibrating dynamic topography estimates from global convection studies.
The Bulhoek carbonatite complex, South Africa: evidence for magmatic crystallization of dolomite at low pressures and the petogenetic implications.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 5-7.
Africa, South Africa
deposit - Bulhoek
Abstract: In many plutonic carbonatite complexes the dominant carbonatite type is calcitic and there is a tendency to assume that dolomitic carbonatites are insignificant relative to calcitic types. While calcitic carbonatites dominate in regions of rifting, e.g. the East African Rift System, dolomitic carbonatites are more abundant in the Archaean Kaapvaal and Zimbabwean Cratons of southern Africa and the Archaean parts of the Canadian Shield (Harmer and Gittins, 1997). The ~1.4Ga Newania carbonatite, the only dolomite carbonatite complex described from India, is located within the Archaean Aravalli Craton (Ray et al., 2013). Increased exploration activity on carbonatites in response to the short-lived 2009-2012 REE boom has highlighted the importance of dolomitic carbonatites as targets for REE (and P) deposits: for example, of the 10 advanced African REE projects (i.e. deposits with a defined resource) associated with carbonatites, 7 are hosted within dolomite carbonatites (Harmer and Nex, 2016). This study reports a detailed petrological study of the Bulhoek Carbonatite Complex, one of a number of carbonatite and alkaline igneous complexes that were emplaced into the central Kaapvaal Craton at 1.4 Ma (Hanson et al., 2006). The Bulhoek Complex comprises three centres of intrusion of magnesian carbonatite into granitic and granophyric components of the 2.05Ga Bushveld Complex over a linear 20 km long zone. At all three centres, areas of fenitised granite enclose sheeted intrusions of dolomitic carbonatite of similar composition and intrusive style. No alkaline silicate magmatic rocks have been in the vicinity of the intrusive centres. Carbonatites were emplaced in three discrete intrusive episodes: initial intrusion was accompanied by significant shattering of the country rocks and produced a sequence of medium-grained, flow foliated dolomite carbonatites (C1) containing clasts of fenitised country rock granites along with xenoliths of fenitised ferrogabbro and magnetite transported from Bushveld Upper Zone cumulates underlying the granites. A second intrusive pulse produced cross-cutting sheets of medium- to coarse-grained dolomitic carbonatite free of xenoliths (C2) that make up the bulk of the carbonatite at each intrusive centre. Evidence that both C1 and C2 carbonatites intruded as crystal-rich mushes include strongly developed sub-vertical foliations, deflection of foliations around large fenite xenoliths and the common occurrence of folded foliations through drag effects at contacts with country rock and in C2 intrusions along contacts with C1 carbonatites.
Abstract: Geodynamics of crustal growth and evolution consist in one of the thorniest questions of the early Earth. In order to solve it, Archean cratons are intensively studied through geophysical, geochemical and geochronological investigations. However, timing and mechanisms leading to accretion and stabilization of crustal blocks are still under question. In this study, new information on the evolution of Archean cratons is provided through complementary approaches applied to the northern margin of the Archean Kaapvaal craton (KC). The study area comprises the Pietersburg Block (PB) and the terrane immediately adjacent to the North: the Southern Marginal Zone of the Limpopo Complex (SMZ). We present a comprehensive petro-metamorphic study coupled with LA-ICP-MS U-Pb isotope examination of both Na- and K-rich granitoids from the two areas. This dataset points toward a new interpretation of the northern KC (PB?+?SMZ). Two significant magmatic events are newly recognized: (i) a ca. 3.2?Ga event, and (ii) a protracted magmatic event between ca. 2.95–2.75?Ga. These events affected in both investigated areas and are unrelated to the ca. 2.7?Ga-old event usually attributed to the SMZ. More importantly, phase equilibrium modelling of several lithologies from the SMZ basement points to middle-amphibolite facies conditions of equilibration instead of granulite-facies conditions historically assumed. This study has both important regional and global implications. Firstly, the presence of a continuous basement from the Thabazimbi-Murchison Lineament to the Palala Shear Zone, different than Central Zone of the Limpopo Complex basement, implies a complete reviewing of the whole Limpopo Complex concept. Secondly, the geometry observed in the northern Kaapvaal craton is assumed to testify for a complete accretionary orogenic sequence with formation of both mafic and TTG lithologies through arc-back arc geodynamic. This was followed by a long-lived lateral compression triggering partial melting of the lower continental crust and emplacement of Bt-granitoids bodies that stabilizes the continental crust. Lastly, partial melting of the underlying enriched mantle stabilized the entire lithosphere allowing long-term preservation of the crustal block.
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) xenoliths are transported from the deep-cratonic lithosphere to the Earth's surface by Cretaceous kimberlites emplaced in the Kimberley area of the Kaapvaal Craton. MARID xenoliths have high modal abundances (70-80?vol%) of mica and amphibole, indicating their origin from a hydrous source. The ?18O values (4.7????18O???6.9‰) of phlogopite micas from 14 MARID samples indicate that these minerals are both 18O-enriched and 18O-depleted with respect to the average upper mantle ?18O value of 5.8?±?0.6‰. The range of ?2H values of phlogopites (?83????2H????53‰, n?=?14) of MARID xenoliths are slightly larger than the average mantle ?2H value (?70?±?10‰). The oxygen (?18Ophlogopites-amphibole?=??0.4 and 0.4‰) and hydrogen (?2Hphlogopite-amphibole?=?14 and 36‰) isotopic disequilibrium recorded from two MARID xenoliths suggests the duration of the last isotopic exchange, possibly just before the kimberlite emplacement, between these minerals and metasomatic fluids was too short to reach isotopic equilibrium. Our model calculation indicates that the phlogopites of MARID xenoliths underwent isotopic exchange with fluids of ?18O?=?5.5 to 10‰, ?2H?=??62 to ?90‰. The range of ?18O value of the calculated metasomatic fluids resembles the oxygen isotopic composition of the primary mantle carbonate (~ 6-9‰) suggesting interaction between carbonatic melt and MARID xenoliths in the continental lithospheric mantle. Furthermore, ?18O values of phlogopites together with previously published nitrogen isotope data (?11 ? ?15N ? 9‰; Banerjee et al., 2015) indicates incorporation of inhomogeneously distributed recycled crustal material from subducted crust within their source magma. Therefore, O-H-N isotope data for MARID xenoliths indicates their crystallization from geochemically heterogeneous magma in the upper continental mantle and subsequent metasomatism with mantle fluids.
Earth and Planetary Science Letters, Vol. 401, pp. 132-147.
Africa, South Africa
metasomatism
Abstract: The Karoo igneous rocks (174-185 Ma) of southern Africa represent one of the largest continental flood basalt provinces on Earth. Available evidence indicates that Karoo magmas either originated in the asthenosphere and were extensively modified by interaction with the lithospheric mantle prior to emplacement in the upper crust; or were produced by partial melting of enriched mantle lithosphere. However, no direct evidence of interaction by Karoo melts (or their precursors) with lithospheric mantle rocks has yet been identified in the suites of mantle xenoliths sampled by post-Karoo kimberlites in southern Africa. Here we report U-Pb ages for lindsleyite-mathiasite (LIMA) titanate minerals (crichtonite series) from three metasomatised, phlogopite and clinopyroxene-rich peridotite xenoliths from the ?84 Ma Bultfontein kimberlite (Kimberley, South Africa), located in the southern part of the Karoo magmatic province. The LIMA minerals appear to have formed during metasomatism of the lithospheric mantle by fluids enriched in HFSE (Ti, Zr, Hf, Nb), LILE (K, Ba, Ca, Sr) and LREE. LIMA U-Pb elemental and isotopic compositions were measured in situ by LA-ICP-MS methods, and potential matrix effects were evaluated by solution-mode analysis of mineral separates. LIMA minerals from the three samples yielded apparent U-Pb ages of , and (). A single zircon grain extracted from the ?190 Ma LIMA-bearing sample produced a similar U-Pb age of , within uncertainty of the LIMA ages. These data provide the first robust evidence of fluid enrichment in the lithospheric mantle beneath the Kimberley region at ?180-190 Ma, and suggest causation of mantle metasomatism by Karoo melts or their precursor(s). The results further indicate that U-Pb dating of LIMA minerals provides a new, accurate tool for dating metasomatic events in the lithospheric mantle.
Earth and Planetary Science Letters, Vol. 482, pp. 253-264.
Africa, South Africa
metasomatism
Abstract: Radiogenic isotope variations unrelated to radiogenic ingrowth are common between minerals found in metasomatised mantle xenoliths entrained in kimberlite, basalts and related magmas. As the metasomatic minerals are assumed to have been in isotopic equilibrium originally, such variations are typically attributed to contamination by the magma host and/or interaction with mantle fluids during or before xenolith transport to surface. However, the increasing evidence of metasomatism by multiple, compositionally distinct fluids permeating the lithospheric mantle, coeval with specific magmatic events, suggests that isotopic disequilibrium might be a consequence of discrete, though complex, metasomatic events. Here we provide clear evidence of elemental and Sr isotope heterogeneity between coeval Ti-rich LIMA (lindsleyite–mathiasite) minerals at the time of their formation in the mantle. LIMA minerals occur in close textural association with clinopyroxene and phlogopite in low-temperature (?800–900?°C), strongly metasomatised mantle xenoliths from the ?84 Ma Bultfontein kimberlite (South Africa). Previous U/Pb dating of the LIMA phases was used to argue that each xenolith recorded a single event of LIMA crystallisation at ?180–190 Ma, coeval with the emplacement of Karoo magmas. SEM imaging reveals that up to four types of LIMA phases coexist in each xenolith, and occasionally in a single LIMA grain. Major element and in situ Sr isotope analyses of the different LIMA types show that each phase has a distinct elemental composition and initial 87Sr/86Sr ratio (e.g., 0.7068–0.7086 and 0.7115–0.7129 for two LIMA types in a single xenolith; 0.7053-0.7131 across the entire sample suite). These combined age and isotopic constraints require that multiple fluids metasomatised these rocks at broadly the same time (i.e. within a few thousands to millions of years), and produced similar mineralogical features. Elemental and isotopic variations between different LIMA types could be due to interaction between one (or more) Karoo-related Ti-rich silicate melts and previously metasomatised, phlogopite-rich lithospheric mantle. This study demonstrates that mantle metasomatic assemblages seemingly generated in a single event may instead result from the infiltration of broadly coeval fluids with variable compositions. This in turn implies that the isotopic variations recorded in mantle rocks may be an inherent feature of metasomatism, and that hot fluids infiltrating a rock do not necessarily cause equilibration at the cm scale, as has been assumed previously. Simple modelling of solid-state diffusion in mantle minerals shows that isotopic disequilibrium may be preserved for up to hundreds of Myr at mantle lithosphere temperatures (?1100–1200?°C), unless subsequently affected by transient heating and/or fluid infiltration events. Radiogenic isotope disequilibrium associated with mantle metasomatism may therefore be a common feature of mantle xenoliths.
Abstract: The compositions of kimberlite melts at depth and upon emplacement in the upper crust remain elusive. This can be attributed to the unquantified effects of multiple processes, such as alteration, assimilation, xenocryst contamination, and fractional crystallisation. The inability to accurately constrain the composition and physical properties of kimberlite melts prevents a comprehensive understanding of their petrogenesis. To improve constraints on the compositions of kimberlite melts, we have combined modal analysis including the discrimination of xenocrystic from magmatic phases, with mineral chemistry determinations to reconstruct a whole-rock composition. We apply this approach to a sample of “fresh” macrocrystic hypabyssal kimberlite (sample BK-1) from the Bultfontein mine (Kimberley, South Africa). The accuracy of this whole-rock reconstruction method is validated by the similarity between reconstructed and measured whole-rock compositions. A series of corrections are then applied to account for the effects of post-emplacement serpentinisation, pre-emplacement olivine crystallisation, and the inclusion and assimilation of mantle material. This approach permits discernment of melt compositions at different stages of kimberlite evolution. The primitive melt parental to the Bultfontein kimberlite is estimated to contain 17.4-19.0?wt% SiO2, 20.2-22.8?wt% MgO, 20.9-21.9?wt% CaO, 2.1-2.3?wt% P2O5, 1.2-1.4?wt% TiO2, 0.9-1.1?wt% Al2O3, and 0.6-0.7?wt% K2O, and has a Mg# of 83.4-84.4. Primary volatile contents (i.e., after an attempt to account for volatile loss) are tentatively estimated at ~2.1-2.2?wt% H2O and ~22.9-25.4?wt% CO2. This composition is deficient in SiO2, MgO and H2O, but enriched in CaO and CO2 compared with most previous estimates of primitive kimberlite melts. We suggest that the primitive melt parental to the Bultfontein kimberlite was a transitional silicate-carbonate melt, which was progressively enriched in SiO2, MgO, Al2O3, Cr2O3, and Na2O through the assimilation of lithospheric mantle material. Comparisons with experimentally produced low-degree melts of carbonated lherzolite indicate that the Bultfontein kimberlite could have formed by ~0.5% melting of asthenospheric mantle at ~6.0-8.6?GPa (i.e., ~190-285?km) and ~1400-1500?°C. The low calculated Na2O contents (<0.2?wt%), which are inconsistent with derivation from low-degree melting of lherzolite, suggest that an alkali-bearing, volatile-rich fluid was exsolved during ascent or released after emplacement, and subsequently removed.
gssaconferences.co.za /compliance -jse-reporting, June 28,29 th
Africa, South Africa
diamond resource and reserve reporting
Abstract: This two-day Workshop (28th and 29th June 2018) comprises an introduction to the SAMREC and SAMVAL Codes, and JSE Reporting. This course is aimed at geologists, mining engineers and other technical specialists, who include sign-off as Competent Persons ("CPs") or Competent Valuators ("CVs") in their job description. Day one focuses on the basics of the SAMREC and SAMVAL Codes, and concentrates on the requirements for CPs who compile documents, specifically Competent Persons Reports and Integrated Annual Reports, for companies listed on the Johannesburg Stock Exchange (applicable primarily to Solid Minerals). Day two focuses on the Section 12 Listing rules applicable to both the Main Board and the Alt-X as well as the requirements of SAMREC and SAMVAL, highlighting some of the issues experienced by CPs over the years as well as some of the updated requirements as a result of the implementation of the 2016 SAMREC/SAMVAL Codes. An introduction to the JSE Readers Panel and a discussion of some of the on-going compliance issues identified by the panel.
South African Journal of Geology, Vol. 120, 1, pp. 1-20.
Africa, South Africa
deposit - Jagersfontein
Abstract: Our earlier studies continued in a diligent search for rare ultradeep xenoliths in the kimberlite diatreme at Jagersfontein. The search has met with moderate success insofar as 20 majorite-bearing (decomposed to *gt + lamellar px) xenoliths are identified. Discrete gts (1 to 2 cm), gt-rich layers (2 to 3 cm) in lherzolites, and rare megacrystic gts (>3 cm) from xenoliths characterize the ultradeep suite. Pyroxene lamellae are crystallographically controlled along {111} gt planes, but px may also be prismatic, lensoidal, coarsely graphic, or annular to gt; jigsaw, rather than 120° dihedral textures, are typical. Gt ranges from Pyr68-74 mole% and CaO - Cr2O3 relations, with two exceptions, are distinctly lherzolitic. Cpx = Wo37-46 mole%, Jd3-19 mole%, with 0.4 to 2.4 wt% Cr2O3; opx = 92 to 95 mole% en, and ol averages 92.5 mole% with maximum wt% 0.1 CaO, 0.4 NiO, and 0.1 Cr2O3. A new class of 10 ultradeep xenoliths has lamellar spinel (Cr/Cr + Al = 0.74; Mg/Mg + Fe = 0.58) in addition to cpx with gt >3wt% Cr2O3 (c.f. 0.5 to 1.5 for sp-free types). Five samples are texturally linked but are compositional outliers to the central body of data: two are sp hosts (Cr# 0.69, Mg# 0.76) and (Cr# 0.74, Mg# 0.57) to gt (Pyr72) + cpx (Jd14); one is a gt megacryst (Pyr80) with sp (Cr# 57, Mg# 69); and the remaining two are unusually rich in chromium with gt = 7.3 to 8.2 wt% Cr2O3, rimmed by cpx (2.3 to 3-3 wt% Cr2O3). In addition, there are 17 xenoliths with compositional affinities to the ultradeep suite but lacking the texturally diagnostic lamellar intergrowths of cpx in gt are possibly completely equilibrated to gt + irregular cpx. Results from the new collection substantiate our earlier conclusions that the mantle was sampled by thejagersfontein kimberlite from the lower lithosphere (250 to 350 km) and the transition zone (435 km) with diagnostic high P-T majorite in lherzolite that decomposed to gt + px at one or more interruptive stations (e.g. lithosphere-asthenosphere boundary), and at one or another time, en route to the surface. Homogeneous majorite occurs as diamond inclusions at Jagersfontein but these are eclogitic, leading to the proposition that the source region in the asthenosphere was an unassimilated mixture of lherzolite and eclogite in the Mid-Cretaceous at the time of kimberlite sampling. Important questions arise: Is majorite primordial; did majorite form exclusively from the transition of pyroxene; or did subsequent dissolution into coexisting garnet take place? Why has majorite not been identified in eclogite, nor diamonds of lherzolitic affinity? Does the formation of majorite and the crystallization of encapsulating diamond imply distinct high P-T events?
South African Journal of Geology, Vol. 120, 3, pp. 371-384.
Africa, Zimbabwe, South Africa
diamond morphology
Abstract: The morphological, chemical impurities and carbon isotope properties of diamonds may reveal subtle details of their mantle source and growth characteristics, supporting efforts towards identifying their original place of harvesting. Here we investigate the mantle carbon and nitrogen sources and growth patterns from selected diamonds mined from four kimberlites: macro-sized diamonds from River Ranch kimberlite in Zimbabwe and the Swartruggens and Klipspringer kimberlitic deposits from South Africa, and micro-sized diamonds from the Klipspringer and Premier kimberlite intrusions in South Africa. Type IaAB diamonds are found in all the samples; Type IaB diamonds only occur in samples from the Swartruggens, River Ranch and Premier kimberlites. A single Type II diamond (nitrogen below the detection limit) was also observed in the River Ranch and Premier kimberlites. Both the micro- and macro-sized diamonds from Klipspringer have similar nitrogen contents. Based on the % B-defect, the diamonds from Klipspringer are grouped into low- and high-nitrogen aggregates (i.e. % of B-defect <40% and >56%, respectively) that likely represent two different diamond forming episodes. Time averaged mantle storage temperatures for Type IaAB diamonds are calculated to have been: 1060°C for Swartruggens; 1190°C for River Ranch; 1100°C (low aggregated); and 1170°C (highly aggregated) for Klipspringer, and 1210°C for Premier diamonds. The CL-images of the River Ranch, Klipspringer and Premier diamonds reveal multi-oscillatory growth zones. The carbon isotopic analyses on the diamonds reveal an average ?13CVPDB value of: -4.5‰ for Swartruggens; -4.7‰ for River Ranch; -4.5‰ for Klipspringer; and -3‰ for Premier. With the exception of the diamond from Premier, the average ?13C value of the diamonds are similar to the average ?13C value of the mantle (-5‰), which is similar to the occurrence of diamonds in the other kimberlites. The internal carbon isotopic variation of individual diamonds from Swartruggens, Klipspringer and Premier are less than 4‰, which is similar to the variability of most other diamond occurrences reported from elsewhere in the world. Up to 6.7‰ internal carbon isotopic variation was observed in a single diamond from River Ranch. The internal carbon isotopic studies of the diamonds reveal that the primary carbon in the Swartruggens and Klipspringer was derived from an oxidation of CH4-bearing fluid, whereas in the River Ranch the primary carbon was derived from the reduction of carbonate-or CO2-bearing fluids. The Swartruggens diamonds also reveal a secondary carbon sourced from a reduction of CO2- or carbonate-rich fluid or melt. Diamonds from Klipspringer exhibit a cyclic change in ?13C values that reflects fluctuation in a complex mantle perturbation system or periodic change in fugacity of the mantle. Based on this study, we conclude that, in principle, a selected range of diamond signatures might be used to fingerprint their origins; especially when linked to their other physical properties such as a low temperature magnetic signature.
Abstract: The mantle beneath the Cullinan kimberlite (formerly known as "Premier") is a unique occurrence of diamondiferous cratonic mantle where diamonds were generated contemporaneously and shortly following a mantle upwelling that led to the formation of a Large Igneous Province that produced the world's largest igneous intrusion - the 2056?Ma Bushveld Igneous Complex (BIC). We studied 332 diamond inclusions from 202 Cullinan diamonds to investigate mantle thermal effects imposed by the formation of the BIC. The overwhelming majority of diamonds come from three parageneses: (1) lithospheric eclogitic (69%), (2) lithospheric peridotitic (21%), and (3) sublithospheric mafic (9%). The lithospheric eclogitic paragenesis is represented by clinopyroxene, garnet, coesite and kyanite. Main minerals of the lithospheric peridotitic paragenesis are forsterite, enstatite, Cr-pyrope, Cr-augite and spinel; the sublithospheric mafic association includes majorite, CaSiO3 phases and omphacite. Diamond formation conditions were calculated using an Al-in-olivine thermometer, a garnet-clinopyroxene thermometer, as well as majorite and Raman barometers. The Cullinan diamonds may be unique on the global stage in recording a cold geotherm of 40?mW/m2 in cratonic lithosphere that was in contact with underlying convecting mantle at temperatures of 1450-1550?°C. The studied Cullinan diamonds contain a high proportion of inclusions equilibrated at temperatures exceeding the ambient 1327?°C adiabat, i.e. 54% of eclogitic diamonds and 41% of peridotitic diamonds. By contrast, ? 1% of peridotitic diamond inclusions globally yield equally high temperatures. We propose that the Cullinan diamond inclusions recorded transient, slow-dissipating thermal perturbations associated with the plume-related formation of the ~2?Ga Bushveld igneous province. The presence of inclusions in diamond from the mantle transition zone at 300-650?km supports this view. Cullinan xenoliths indicative of the thermal state of the cratonic lithosphere at ~1.2?Ga are equilibrated at the relatively low temperatures, not exceeding adiabatic. The ability of diamonds to record super-adiabatic temperatures may relate to their entrainment from the deeper, hotter parts of the upper mantle un-sampled by the kimberlite in the form of xenoliths or their equilibration in a younger lithosphere after a decay of the thermal disturbance.
Reviews of African Political Economy, Vol. 44, 152, pp. 272-291.
Africa, South Africa
history
Abstract: This article examines the history of South African mining over the last 30 years. It notes the declining contribution of mining to the economy, and a drop in employment levels and labour migration. It considers political, legislative and macro-economic changes, as well as mine ownership and control. It addresses the question why a democratically elected government, progressive labour legislation, trade-unionisation and Black Economic Empowerment have made remarkably little difference to working conditions. After examining the trajectories of individual commodities, such as gold, platinum, coal and diamonds, it concludes there has been no fundamental change in the relationship between state and capital.
The Journal of the Southern African Institute of Mining and Metallurgy, Vol. 118, Jan. pp. 1-6.
Africa, South Africa
diamond size frequency
Abstract: Diamond size frequency distribution (SFD) curves, combined with the associated dollar per carat per size class, play an important role in the diamond industry. Value per size class is unique for each deposit and typically varies from less than a dollar per carat to several thousands of dollars per carat for special stones. Recovery of large stone therefore contributes significantly to the bottom line of a large diamond producer. While the design of the process plant should prevent damage and possible breakage of large stones, it should also ensure adequate liberation of the finer diamonds. Innovative solutions are required to protect and recover type I and II diamonds if prominent within the resource. X-ray transmission (XRT) sorting presents the opportunity to develop flow sheet designs that incorporate a balance between exploitation of the resource and process efficiency, as well as practical capital and operating costs. This paper serves to illustrate the role and application of SFD curves in determining optimum cut-off and re-crush sizes within the flow sheet of a large diamond producer. A thorough understanding of the unique technical and economic aspects of a deposit provides the basis from where new and innovative technologies can be proposed, allowing mining companies to maintain and improve profit margins. It highlights the results of various plant trials and newly commissioned XRT sorters for larger size fractions. It also provides recommendations for future applications of XRT machines in the diamond process flow sheet.
Abstract: It is well established that the cratonic subcontinental lithospheric mantle (C-SCLM) represents a residue of extensively melted peridotite. The widespread occurrence of garnet in C-SCLM remains a paradox because experiments show that it should be exhausted beyond ?20% melting. It has been suggested that garnet may have formed by exsolution from Al-rich orthopyroxene; however, the few documented examples of garnet exsolution in cratonic samples are exotic and do not afford a direct link to garnet in granular harzburgite. We report crystallographic, petrographic, and chemical data for an exceptionally well preserved orthopyroxene megacryst containing garnet lamellae, juxtaposed against granular harzburgite. Garnet lamellae are homogeneously distributed within the host orthopyroxene and occur at an orientation that is unrelated to orthopyroxene cleavage, strongly indicating that they formed by exsolution. Garnet lamellae are subcalcic Cr-pyrope, and the orthopyroxene host is high-Mg enstatite; these phases equilibrated at 4.4 GPa and 975 °C. The reconstructed precursor is a high-Al enstatite that formed at higher pressure and temperature conditions of ?6 GPa and 1750 °C. The megacryst shows evidence for disintegrating into granular peridotite, and garnet and orthopyroxene within the granular peridotite are texturally and chemically identical to equivalent phases in the megacryst. Collectively, this evidence supports a common origin for the granular and exsolved portions of the sample. We hypothesize that high-Al enstatite was a common phase in the C-SCLM and that exsolution during cooling and stabilization of the C-SCLM could be the origin of most subcalcic garnets in depleted peridotites.
Earth Planetary Science Letters, Vol. 491, pp. 134-147.
Africa, South Africa
deposit - De Beers-Pool
Abstract: Fluid/melt inclusions in diamonds, which were encapsulated during a metasomatic event and over a short period of time, are isolated from their surrounding mantle, offering the opportunity to constrain changes in the sub-continental lithospheric mantle (SCLM) that occurred during individual thermo-chemical events, as well as the composition of the fluids involved and their sources. We have analyzed a suite of 8 microinclusion-bearing diamonds from the Group I De Beers Pool kimberlites, South Africa, using FTIR, EPMA and LA-ICP-MS. Seven of the diamonds trapped incompatible-element-enriched saline high density fluids (HDFs), carry peridotitic mineral microinclusions, and substitutional nitrogen almost exclusively in A-centers. This low-aggregation state of nitrogen indicates a short mantle residence times and/or low mantle ambient temperature for these diamonds. A short residence time is favored because, elevated thermal conditions prevailed in the South African lithosphere during and following the Karoo flood basalt volcanism at ?180 Ma, thus the saline metasomatism must have occurred close to the time of kimberlite eruptions at ?85 Ma. Another diamond encapsulated incompatible-element-enriched silicic HDFs and has 25% of its nitrogen content residing in B-centers, implying formation during an earlier and different metasomatic event that likely relates to the Karoo magmatism at ca. 180 Ma. Thermometry of mineral microinclusions in the diamonds carrying saline HDFs, based on Mg-Fe exchange between garnet-orthopyroxene (Opx)/clinopyroxene (Cpx)/olivine and the Opx-Cpx thermometer, yield temperatures between 875-1080?°C at 5 GPa. These temperatures overlap with conditions recorded by touching inclusion pairs in diamonds from the De Beers Pool kimberlites, which represent the mantle ambient conditions just before eruption, and are altogether lower by 150-250?°C compared to P-T gradients recorded by peridotite xenoliths from the same locality. Oxygen fugacity differs as well. The calculated for the saline HDF compositions (to ?1.34) are higher by about a log unit compared with that recorded by xenoliths at 4-7 GPa. We conclude that enriched saline HDFs mediated the metasomatism that preceded Group I kimberlite eruptions in the southwestern Kaapvaal craton, and that their ‘cold and oxidized’ nature reflects their derivation from a deep subducting slab. This event had little impact on the temperature and redox state of the Kaapvaal lithosphere as a reservoir, however, it likely affected its properties along limited metasomatized veins and their wall rock. To reconcile the temperature and oxygen fugacity discrepancy between inclusions in diamonds and xenoliths, we argue that xenoliths did not equilibrate during the last saline metasomatic event or kimberlite eruption. Thus the P-T-gradients they record express pre-existing lithospheric conditions that were likely established during the last major thermal event in the Kaapvaal craton (i.e. the Karoo magmatism at ca. 180 Ma).
Mineralogy and Petrology, in press available, 14p.
Africa, South Africa
deposit - Bultfontein
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) and PIC (Phlogopite-Ilmenite-Clinopyroxene) xenoliths are thought to be formed by intense Bprimary^ mantle metasomatism. These rocks also display secondary features, such as cross-cutting veins and geochemical zonation of matrix minerals, which probably reflect latermetasomatic events. To investigate the nature and origin(s) of these secondary features, 28 MARID and PIC xenoliths from southern African kimberlites and orangeites have been studied. MARID-hosted veins contain both carbonate and Ti-rich phases (e.g., titanite, phlogopite), suggesting that they formed by the infiltration of a carbonated silicate melt. Elevated TiO2 contents in MARID matrix mineral rims are spatially associated with carbonate-dominated veins, suggesting a genetic relationship between vein formation and geochemical zonation. Spongy rims around primaryMARID and PIC clinopyroxene are depleted in Na2O andAl2O3 relative to their cores, possibly reflecting mineral dissolution in the xenoliths during ascent and emplacement of the entraining kimberlite. The preservation of compositional differences between primary and secondary phases in MARID and PIC xenoliths indicates that metasomatism occurred shortly before, or broadly coeval with, kimberlite/orangeite magmatism; otherwise, at typical mantle temperatures, such features would have quickly re-equilibrated. Increased Na2O in some mineral rims (e.g., K-richterite) may therefore reflect equilibration with a more Na-enriched primitive kimberlite melt composition than is commonly suggested. Vein-hosted clinopyroxene 87Sr/86Sri (0.70539 ± 0.00079) in one MARID sample is intermediate between primary clinopyroxene in the sample (0.70814 ± 0.00002) and the host Bultfontein kimberlite (0.70432 ± 0.00005), suggesting that vein minerals are derived from interactions between primary MARID phases and kimberlite-related melts/fluids. Sulfur isotope compositions of barite (?34SVCDT = +4.69 ‰) and sulfides (?34SVCDT = ?0.69 ‰) in carbonate veins reflect equilibration at temperatures of 850-900 °C, consistent with sulfurrich melt/fluid infiltration in the lithospheric mantle. In contrast, vein carbonate C-O isotope systematics (?13CVPDB = ?9.18 ‰ ?18OVSMOW = +17.22‰) are not typical of kimberlites or other mantle carbonates (?13CVPDB = ?3 to ?8‰ ?18OVSMOW = 6 to 9 ), and may represent post-emplacement hydrothermal interactions of the cooling kimberlite with crustal fluids. These constraints suggest protracted metasomatism of MARID rocks shortly before and during entrainment by the host kimberlite.
Geophysical Research Abstracts www.researchgate.net, Vol. 20, EGU2018-128291p. Abstract
Africa, South Africa
diamond inclusions
Abstract: Changing recycling budgets of surface materials and volatiles by subduction of tectonic plates influence the compositions of Earth’s major reservoirs and affect climate throughout geological time. Fluids play a key role in processes governing subduction recycling, but quantifying the exact fate of volatiles introduced into the mantle at ancient and recent destructive plate boundaries remains difficult. Here, we report on the role of fluids and the fate of volatiles and other elements at two very different tectonic settings: 1) at subduction settings, and 2) within the subcontinental lithospheric mantle (SCLM). We will show how olivine-hosted melt inclusions from subduction zones and mineral inclusions in diamond from the SCLM are used to reveal how changing tectonic settings influence volatile cycles with time. Melt inclusions from the complex Italian post-collisional tectonic setting are used to identify changing subduction recycling through time. The use of CO2 in deeply trapped melt inclusions instead of in lavas or volcanic gases provides a direct estimate of deep recycling, minimizing possible effects of contamination during transfer through the crust. The aim is to distinguish if increased recycling of sediments from the down-going plate at continental subduction settings results in increased deep CO2 recycling or if the increased CO2 flux results from crustal degassing of the overriding plate. Both processes likely affected climate through Earth history but could thus far not be discriminated. The study of mineral inclusions and their host diamonds from the SCLM can link changes in the cycling of carbon-rich fluids and the time and process through which the carbon redistribution took place. We use Sm-Nd isotope techniques to date the mineral inclusions and use the carbon isotope data of the host diamonds to investigate the growth conditions. I will present case-studies of peridotitic and eclogitic diamonds from three mines in Southern Africa.
Mineralogy and Petrology, 10.1007/ s00710-018- 0589-4, 14p.
Africa, South Africa, Canada, Northwest Territories, Ontario
deposit - Venetia, Voorspoed, Gahcho Kue, Victor, Snap Lake
Abstract: De Beers kimberlite mine operations in South Africa (Venetia and Voorspoed) and Canada (Gahcho Kué, Victor, and Snap Lake) have the potential to sequester carbon dioxide (CO2) through weathering of kimberlite mine tailings, which can store carbon in secondary carbonate minerals (mineral carbonation). Carbonation of ca. 4.7 to 24.0 wt% (average?=?13.8 wt%) of annual processed kimberlite production could offset 100% of each mine site’s carbon dioxide equivalent (CO2e) emissions. Minerals of particular interest for reactivity with atmospheric or waste CO2 from energy production include serpentine minerals, olivine (forsterite), brucite, and smectite. The most abundant minerals, such as serpentine polymorphs, provide the bulk of the carbonation potential. However, the detection of minor amounts of highly reactive brucite in tailings from Victor, as well as the likely presence of brucite at Venetia, Gahcho Kué, and Snap Lake, is also important for the mineral carbonation potential of the mine sites.
Mineralogy and Petrology, 10.1007/ s00710-018- 0568-9, 15p.
Africa, South Africa
geochronology
Abstract: The West Coast of Namaqualand in South Africa hosts extensive detrital diamond deposits, but considerable debate exists as to the provenance of these diamonds. Some researchers have suggested derivation of the diamonds from Cretaceous-Jurassic kimberlites (also termed Group I kimberlites) and orangeites (also termed Group II kimberlites) located on the Kaapvaal Craton. However, others favour erosion of diamonds from the ca.300 Ma Dwyka Group sediments, with older, pre-Karoo kimberlites being the original source(s). Previous work has demonstrated that 40Ar/39Ar analyses of clinopyroxene inclusions, extracted from diamonds, yield ages approaching the time(s) of source kimberlite emplacement, which can be used to constrain the provenance of placer diamond deposits. In the current study, 40Ar/39Ar analyses were conducted on clinopyroxene inclusions from two similar batches of Namaqualand detrital diamonds, yielding (maximum) ages ranging from 117.5?±?43.6 Ma to 3684?±?191 Ma (2?) and 120.6?±?15.4 Ma to 688.8?±?4.9 Ma (2?), respectively. The vast majority of inclusions (88%) produced ages younger than 500 Ma, indicating that most Namaqualand diamonds originated from Cretaceous-Jurassic kimberlites/orangeites, with few, if any, derived from the Dwyka tillites. The provenance of the Namaqualand diamonds from ca.115-200 Ma orangeites is consistent with Late Cretaceous paleo-drainage reconstructions, as these localities could have been sampled by the ‘paleo-Karoo’ River and transported to the West Coast via an outlet close to the current Olifants River mouth. At ca.90 Ma, this drainage system appears to have been captured by the ‘paleo-Kalahari’ River, a precursor to the modern Orange River system. This latter drainage is considered to have transported diamonds eroded from both ca.80-90 Ma kimberlites and ca.115-200 Ma orangeites to the West Coast, which were subsequently reworked along the Namibian coast, forming additional placer deposits.
Mineralogy and Petrology, June 14, DOI:10.1007/ s00710-018 -0595-6, 16p.
Africa, South Africa
deposit - Boshof
Abstract: We describe the petrography and mineral chemistry of sixteen eclogite and garnet pyroxenite xenoliths from the reworked Boshof road dump (Kimberley) and define three groups that stem from different depths. Group A, the shallowest derived, has low HREE (heavy rare earth element) abundances, flat middle to heavy REE patterns and high Mg# [= 100•Mg/(Mg?+?Fe)]. Their protoliths probably were higher pressure cumulates (~ 0.7 GPa) of mainly clinopyroxene (cpx) and subordinate orthopyroxene (opx) and olivine (ol). Group B1 xenoliths, derived from the graphite/diamond boundary and below show similarities to present-day N-MORB that were modified by partial melting (higher Mg# and positively inclined MREE (middle REE) and HREE (heavy REE) patterns of calculated bulk rocks). Group B2 samples from greatest depth are unique amongst eclogites reported so far worldwide. The calculated bulk rocks have humped REE patterns with very low La and Lu and prominent maxima at Sm or Eu and anomalously high Na2O (up to 5 wt%) which makes protolith identification difficult. The complex trace element signatures of the full spectrum of Kimberley eclogites belie a multi-stage history of melt depletion and metasomatism with the introduction of new phases especially of phlogopite (phlog). Phlogopite appears to be characteristic for Kimberley eclogites and garnet peridotites. Modelling the metasomatic overprint indicates that groups A and B1 were overprinted by volatile- and potassium-rich melts probably by a process of chromatographic fractionation. Using constraints from other metasomatized Kimberley mantle rocks suggest that much of the metasomatic phlogopite in the eclogites formed during an intense episode of metasomatism that affected the mantle beneath this region 1.1 Gyr ago.
Mineralogy and Petrology, June 14, DOI:10.1007/ s00710-018 -0588-5, 16p.
Africa, South Africa
deposit - De Beers dyke
Abstract: We present petrographic and mineral chemical data for a suite of samples derived from the De Beers dyke, a contemporaneous, composite intrusion bordering the De Beers pipe (Kimberley, South Africa). Petrographic features and mineral compositions indicate the following stages in the evolution of this dyke: (1) production of antecrystic material by kimberlite-related metasomatism in the mantle (i.e., high Cr-Ti phlogopite); (2) entrainment of wall-rock material during ascent through the lithospheric mantle, including antecrysts; (3) early magmatic crystallisation of olivine (internal zones and subsequently rims), Cr-rich spinel, rutile, and magnesian ilmenite, probably on ascent to the surface; and (4) crystallisation of groundmass phases (i.e., olivine rinds, Fe-Ti-rich spinels, perovskite, apatite, monticellite, calcite micro-phenocrysts, kinoshitalite-phlogopite, barite, and baddeleyite) and the mesostasis (calcite, dolomite, and serpentine) on emplacement in the upper crust. Groundmass and mesostasis crystallisation likely forms a continuous sequence with deuteric/hydrothermal modification. The petrographic features, mineralogy, and mineral compositions of different units within the De Beers dyke are indistinguishable from one another, indicating a common petrogenesis. The compositions of antecrysts (i.e., high Cr-Ti phlogopite) and magmatic phases (e.g., olivine rims, magnesian ilmenite, and spinel) overlap those from the root zone intrusions of the main Kimberley pipes (i.e., Wesselton, De Beers, Bultfontein). However, the composition of these magmatic phases is distinct from those in ‘evolved’ intrusions of the Kimberley cluster (e.g., Benfontein, Wesselton water tunnel sills). Although the effects of syn-emplacement flow processes are evident (e.g., alignment of phases parallel to contacts), there is no evidence that the De Beers dyke has undergone significant pre-emplacement crystal fractionation (e.g., olivine, spinel, ilmenite). This study demonstrates the requirement for detailed petrographic and mineral chemical studies to assess whether individual intrusions are in fact ‘evolved’; and that dykes are not necessarily produced by differentiated magmas.
Mineralogy and Petrology, 10.1007/ s710-018- 0603-x 15p.
Africa, South Africa
deposit - Finsch, De Beers Pool, Koffiefontein
Abstract: Fibrous diamond growth zones often contain abundant high-density fluid (HDF) inclusions and these provide the most direct information on diamond-forming fluids. Noble gases are incompatible elements and particularly useful in evaluating large-scale mantle processes. This study further constrains the evolution and origin of the HDFs by combining noble gas systematics with ?¹³C, N concentrations, and fluid inclusion compositions for 21 individual growth zones in 13 diamonds from the Finsch (n = 3), DeBeers Pool (n = 7), and Koffiefontein (n = 3) mines on the Kaapvaal Craton. C isotope compositions range from ?2.8 to ?8.6‰ and N contents vary between 268 and 867 at.ppm, except for one diamond with contents of <30 at.ppm N. Nine of the thirteen studied diamonds contained saline HDF inclusions, but the other four diamonds had carbonatitic or silicic HDF inclusions. Carbonatitic and silicic HDFs yielded low He concentrations, R/Ra (³He/?Hesample/³He/?Heair) values of 3.2–6.7, and low ??Ar/³?Ar ratios of 390–1940. Noble gas characteristics of carbonatitic-silicic HDFs appear consistent with a subducted sediment origin and interaction with eclogite. Saline HDFs are characterised by high He concentrations, with R/Ra mostly between 3.9 and 5.7, and a wide range in ??Ar/³?Ar ratios (389–30,200). The saline HDFs likely originated from subducted oceanic crust with low He but moderate Ar contents. Subsequent interaction of these saline HDFs with mantle peridotite could explain the increase in He concentrations and mantle-like He isotope composition, with the range in low to high ??Ar/³?Ar ratios dependent on the initial ³?Ar content and extent of lithosphere interaction. The observed negative correlation between ?He contents and R/Ra values in saline HDFs indicates significant in situ radiogenic ?He production.
Noble gas geochemistry of fluid inclusions in South African diamonds: implications for the origin of diamond-forming fluids.
Mineralogy and Petrology, doi.org/10.1007/s710-018-0601-z 15p.
Africa, South Africa
deposit - Cullinan
Abstract: We studied a suite of Cullinan diamonds (<0.3 ct) with mineral inclusions, which comprised 266 Type I and 75 blank Type II (<20 ppm N) diamonds, as classified by infrared spectroscopy. More than 90% (n?=?68) of Type II diamonds do not luminesce. In contrast, 51.9% (n?=?177) of Type I diamonds luminesce, with blue colors of different intensity. Carbon isotopic compositions of Type I and II diamonds are similar, with ?13CVPDB ranging from ?2.1 to ?7.7‰for Type I diamonds (n?=?25), and from ?1.3 to ?7.8- for Type II diamonds (n?=?20). The Type II diamonds are sourced from three parageneses, lithospheric lherzolitic (45%), lithospheric eclogitic (33%), and sublithospheric mafic (22%). The lherzolitic suite contains Cr-pyrope, forsterite, enstatite, clinopyroxene and Cr-spinel formed at 1090-1530 °C and P?=?4.6-7.0 GPa. Lithospheric eclogitic diamonds containing garnet, omphacite, kyanite and coesite comprise 33% of Type II diamonds. The sublithospheric mafic paragenesis is mainly represented by Cr-free majorite, various CaSiO3 phases and omphacite equilibrated at 11.6-26 GPa, in the transition zone and the lower mantle. The lherzolitic paragenesis predominates in Type II diamonds, whereas 79% Type I diamonds are sourced from eclogites. The higher incidence of sublithospheric inclusions was found in Type II diamonds, 22% against 6% in Type I diamonds. The similarity of the mineral parageneses and C isotopic compositions in the small Cullinan Type II and Type I diamonds indicate the absence of distinct mantle processes and carbon sources for formation of studied Type II diamonds. The parent rocks and the carbon sources generally vary for Type II diamonds within a kimberlite and between kimberlites.
Abstract: In the mid 1880s a little-known photographer named Robert Harris produced a series of albumen prints showing the stages of body searching that black labourers in De Beers diamond mines were obliged to undergo by state ordinance enacted in 1883. The original photographs surfaced briefly in the sale-room in 2007 but have since disappeared. Two sets of copies survive. Bearing in mind the history of documentary photography in South Africa, this essay examines the historical and textual significance of this series of photographs in the context of the history of mining and discusses the imperatives and ethics of locating, researching and publishing controversial imagery in the internet age.
Geochemistry, Geophysics, Geosystems, Vol. 19, 5, pp. 1499-1518.
Africa, South Africa
craton
Abstract: Cratons, the ancient cores of continents, have an unusually thick lithosphere (the tectonic plate beneath them). At least ?200 km thick, it has a highly anomalous composition, making it less dense than the surrounding mantle. Cratonic lithosphere can thus be cooled to much lower temperatures than elsewhere. Variations in this delicate buoyancy balance probably give rise to variations in the surface elevation across the Earth's stable continents. Lithospheric thickness and composition are key parameters, but both are notoriously difficult to determine. Here we use very accurate measurements of seismic surface?wave velocities and determine deep structure beneath cratons in southern Africa. We discover an unexpectedly strong, gradual thickening of the lithosphere from the central Kaapvaal Craton to the neighboring Limpopo Belt (from 200 to 300 km thick). Curiously, surface elevation decreases monotonically with increasing lithospheric thickness. This demonstrates the effect of the deep lithosphere on topography and gives us new information on the composition of the deepest parts of lithosphere.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0613-8 19p.
Africa, South Africa
deposit - Finsch
Abstract: Microinclusion-bearing diamonds offer the opportunity to investigate relationships between mantle metasomatism, diamond formation and kimberlite eruptions in intracratonic provinces. We have analyzed a suite of 7 microinclusion-bearing diamonds from the Finsch Group II kimberlite, South Africa, and identified two diamond populations: ‘Finsch IaA’ diamonds have nitrogen solely in A-centers and contain saline high-density-fluid (HDF) microinclusions, while ‘Finsch IaAB’ diamonds have nitrogen in both A- and B-centers (25-35% B-centers) and are characterized by carbonatite HDF compositions. Based on nitrogen aggregation states and estimates for mantle residence temperatures, we conclude that ‘Finsch IaA’ diamonds formed during a young saline metasomatic event that preceded kimberlite eruption by ~50 kyr to 15 Myr. The possible timing of metasomatism and formation of ‘Finsch IaAB’ diamonds by carbonatite HDFs is less constrained, and could have taken place between ~15 Myr and 2 Gyr before eruption. Two of the diamonds encapsulated omphacite microinclusions in association with saline or low-Mg carbonatitic-like HDF. We observe compositional differences for Al2O3 vs. CaO between these metasomatised omphacites, and also compared to omphacites in mantle eclogites which were identified as metasomatised by kimberlite or high-Mg carbonatite; suggesting a possible relationship between Al2O3 and CaO in metasomatised omphacite and the type of fluid/melt it interacted with. The combined data for microinclusion-bearing diamonds from the Finsch Group II kimberlite and the neighbouring Group I kimberlites at Koffiefontein and De Beers Pool indicate that a substantial volume of the southwest Kaapvaal deep lithosphere was impacted by saline metasomatism during Cretaceous time, and a direct relationship between saline metasomatism, diamond formation and the Kaapvaal late-Mesozoic ‘kimberlite bloom’. We therefore conclude that saline HDFs play a key role in the buildup of metasomatic mantle sources leading to kimberlite eruptions.
Abstract: Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable 87Sr/86Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted 87Sr/86Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with 87Sr/86Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.
Abstract: Natural-color blue diamonds are among the rarest and most valuable gemstones. Gray and violet diamonds are also included here, as these diamonds can coexist on a color continuum with blue diamonds. More so than most other fancy colors, many diamonds in this color range are sourced from specific locations-the Cullinan mine in South Africa and the Argyle mine in Australia. Although blue color is often associated with boron impurities, the color of diamonds in this range (including gray and violet) also originates from simple structural defects produced by radiation exposure or from more complex defects involving hydrogen. These different mechanisms can be characterized by absorption and luminescence spectroscopy. A fourth mechanism-micro-inclusions of grayish clouds or tiny graphite particles in gray diamonds-can be distinguished through microscopy. In this article, we summarize prior research as well as collected data such as color and carat weight on more than 15,000 naturally colored blue/gray/violet diamonds from the GIA database (along with an analysis of spectroscopic data on a subset of 500 randomly selected samples) to provide an unprecedented description of these beautiful gemstones.
Abstract: We report preliminary results of a systematic search for fluid/melt microinclusions in mantle minerals. “Dusty” garnets from xenolith XRV6 [1], a heavily metasomatised Type I eclogite from Roberts Victor mine, SA, carry many microinclusions (<1 ?m). FTIR analyses of "dusty" zones indicate the presence of molecular water in the inclusions and hydroxyl groups in the garnet. EPMA analysis of 136 microinclusions constrains the bulk composition of the microinclusions. Compared to the host garnet, they are enriched in TiO2, FeO, CaO, Na2O and K2O and depleted in Al2O3 and MgO. The silica contents seem to be similar to that of the host garnet. Figure 1: a. Backscatter image of the microinclusions in XRV6 garnet. b. K2O vs. MgO of the clear garnet (red) and the microinclusions (+ their surrounding garnet, blue). Most of the elements form compositional mixing arrays of microinclusion+garnet (Fig. 1b). The arrays trend away from the compositions of large melt pools or secondary minerals found in the xenolith. They point towards the array of silicic to low-Mg carbonatitic high density fluids (HDFs) trapped in diamonds, indicating the role of such fluids in mantle metasomatism.
Abstract: Polycrystalline diamond aggregates (framesites, boart, diamondite) are an understudied variety of mantle diamond, but can make up 20% of the production in some Group I kimberlites. Their polycrystalline nature indicates rapid precipitation from carbon-oversaturated fluids and individual PDAs often contain a chemically heterogeneous suite of websteritic and pyroxenitic inclusions and minerals intimately intergrown with the diamond crystals. Geochemical and microstructural evidence suggests that fluid-driven redox reactions with lithospheric material occurring episodically over millions of years play a major role in freezing carbon in the subcratonic lithosphere (Jacob et al., 2000; 2016; Mikhail et al., 2014). A suite of 39 samples from the Venetia kimberlite pipe in South Africa allows a more detailed look at the diamondforming fluids. 13C values in the diamonds measured by secondary ion mass spectrometry range from +2 to -28 and cover the entire range for PDA from the literature. Nitrogen concentrations are mostly very low (less than 100 at ppm), but reach up to 2660 at ppm in individual samples. These high nitrogen concentrations in concert with mostly positive 15N values of up to +17 and some very negative 3C values suggest crustal material as the source of the nitrogen and the carbon. However, detailed analysis of the sample provides evidence for a more complex growth history followed by alteration. Individual diamond crystals show complex growth zonations by cathodoluminescence imaging that can be related with the carbon and nitrogen isotopic compositions and points to growth incorporating several pulses of carbon-nitrogen fluid with distinct isotopic compositions. Most of these growth events show decoupled carbon and nitrogen systematics. In addition, EBSD identifies deformation and recrystallization and nitrogen aggregation states range from pure IaA to pure IaB, supporting a heterogeneous and episodic growth history.
Africa, Zimbabwe. Australia, Canada, Northwest Territories, South Africa, Botswana
deposit - Murowa, Argyle, Diavik, Venetia, Orapa
Abstract: FTIR maps of diamond plates, cut through the centre of growth, contain abundant information about changing defect concentrations from core to rim. These data can, in principle, be interpreted in terms of the variation in conditions of diamond growth and the temperatures experienced by the diamond during the period of mantle residence between growth and exhumation. Many diamonds show multiple growth zones that can be observed by cathodoluminescence. Importantly, the combination of nitrogen concentration and nitrogen aggregation measured by FTIR can be used to determine whether the growth zones are of similar or very different ages (Kohn et al., 2016). In this study, we use automated fitting of several thousand individual spectra within each FTIR map to define a model temperature for each pixel using the Python program, QUIDDIT. We then use a two-stage aggregation model to constrain potential temperature-time histories for each diamond. To take full advantage of the temperature history recorded by zoned diamonds, radiometric ages of inclusions are required. If the growth ages of each zone and the date of exhumation are well-known, then a model temperature can be calculated for each zone. The combination of zone-specific ages and improved quality and processing of FTIR spectra is able to provide unique new insights into the thermal history of diamondbearing lithospheric mantle. For the first time we will be able to use the N defects in diamonds to work out whether a particular location in the lithosphere has heated or cooled over long periods of geological time. The implications for the mechanism of formation of lithosphere will be discussed. We will illustrate the approach using examples of zoned diamonds from Murowa (Zimbabwe), Argyle (Australia), Diavik (Canada), Venetia (South Africa) and Orapa (Botswana).
Africa, South Africa, Guinea, South America, Brazil
deposit - Kankan, Jagersfontein, Juina
Abstract: Inclusions in super-deep diamonds provide a unique window to the sublithospheric mantle (e.g. [1-4]). Here we present oxygen isotopes for Kankan majoritic garnet and former bridgmanite inclusions. The clustering of Kankan majorites around a ?18O of +9‰ is nearly identical to those reported from Jagersfontein [1]. This elevated and nearly constant ?18O signal indicates homogenization of partial melts from the uppermost part of altered basaltic slabs. Conversely, ?18O values in Juina majorites are highly variable [2] due to crystallization from small, discrete melt pockets in a heterogeneous eclogitic source. While all these majorites have eclogitic/pyroxenitic Cr2O3 and CaO contents, charge-balance for Si[VI] is achieved very differently, with Jagersfontein [3], Kankan [4], and Juina [2] majorites transitioning from eclogitic Na[VIII]Si[VI] to peridotitic-pyroxenitic [5] Mg[VI]Si[VI] substitutions. We interpret this shift as the result of homogenized eclogitic partial melts infiltrating and reacting with adjacent pyrolitic mantle at Kankan and Jagersfontein. Increases in Mg# and Cr2O3 with reductions in ?18O support this reaction. This model is in agreement with recent experiments in which majorites and diamonds form from a reaction of slab-derived carbonatite with reduced pyrolite at 300-700 km depth [6]. The Kankan diamonds also provide an opportunity to establish the chemical environment of the lower mantle. Four inclusions of MgSiO3, inferred to be former bridgmanite [4], provide the first-measured ?18O values for lower mantle samples. These values suggest derivation from primitive mantle, or unaltered subducted oceanic lithospheric mantle. The Kankan super-deep inclusions thus provide a cross-section of deep mantle that highlights slab-pyrolite reactions in the asthenosphere and primitive compositions in the lower mantle.
Abstract: Volcanic pipes, or maar-diatreme volcanoes, form during explosive eruptions of mantle-derived magmas near Earth's surface. Impressive examples are the carrot-shaped, downward tapering structures formed by kimberlite magmas. Kimberlites originate from >150 km depth within Earth's mantle beneath thick continental roots, away from tectonic plate margins. Kimberlite pipes can be significant diamond deposits, and the complex architecture revealed during exploration and mining is ascribed to repeated magma injections leading to multiple eruptions. Repeated magmatic pulses cause diatremes to widen and grow downward, forming kilometer-sized subterranean structures. However, the time-resolved evolution of kimberlite pipe systems is largely unknown. We present the first U/Pb perovskite ages for newly discovered kimberlite dikes (1139.8 ± 4.8 Ma) that cut through the volcaniclastic infill of the Premier kimberlite pipe (1153.3 ± 5.3 Ma) at Cullinan Diamond Mine, South Africa. The ages reveal that renewed kimberlite volcanic activity occurred, at a minimum, 3 m.y. after the main pipe formation. This finding suggests that the largest kimberlite pipes, and maar-diatreme volcanoes in general, may be magmatically active for several millions of years, which conflicts with this volcanism being described as 'monogenetic' at millennia time scales. Exemplified by Tier-1 diamond deposits on the Kaapvaal craton, long-lasting kimberlite volcanic activity may be an important factor in growing large diatremes, plus enabling effective transport of mantle cargo from the diamond stability field to Earth's surface.
Africa, South Africa, China, United States, Canada, South America
diamond inclusions
Abstract: We present the first evidence for inclusions of ice-VII in diamonds from southern Africa, China, North- and South-America [1]. Combining synchrotron X-ray diffraction, - X-ray fluorescence and IR spectroscopy, we show the presence of ice-VII as inclusions in diamonds that have formed at depth > 410 km to about 800 km in the Earth's mantle. What is now crystalline ice-VII, a high pressure polymorph of water-ice, was component of an aqueous fluid entrapped in the diamonds that were growing in the deep mantle. Because of the confinement by the host diamonds, the inclusions retain high pressures. The same holds for inclusions of magnesian calcite, halite, and ilmenite found in the same diamond specimens. These inclusions reflect the presence of aqueous and carbonaceous fluids in the mantle transition zone and the shallow lower mantle. Using their current residual pressures and the equations of state, we can reconstruct their recovery paths [2,3]. Further, we can use the intersection of modelled recovery paths to better constrain the encapsulation pressure and temperature of these inclusions in diamonds.
Abstract: Mineral and fluid/melt inclusions in diamonds, which are encapsulated and isolated during a metasomatic event, offer the opportunity to constrain changes in the sub-continental lithospheric mantle that occurred during individual thermochemical events. Fibrous diamonds from the Group I De Beers Pool kimberlites, South Africa (SA), trapped incompatibleelement enriched saline high-density fluids (HDFs) and peridotitic mineral microinclusions. Their substitutional nitrogen resides almost exclusively in A-centers. With regard to the elevated thermal conditions that prevailed in the SA lithosphere during and following Karoo volcanism at ~180 Ma, this low-aggregation state of nitrogen suggests a short mantle residence time, constraining the time of saline metasomatism to be close to the eruption of the kimberlites at ~85 Ma. Thermometry of mineral microinclusions yield temperatures between 875-1080 ºC (at 5 GPa). These temperatures overlap with conditions recorded by touching inclusion pairs, which represent the mantle ambient conditions just before eruption, and are altogether lower by 150-250°C compared to P-T gradients recorded by peridotite xenoliths from the same locality. In addition, the oxygen fugacity calculated for the saline HDF compositions (?log??O2(FMQ) = -2.5 to -1.3) are higher by about a log unit compared with that recorded by xenoliths at 4-7 GPa. We conclude that enriched saline HDFs mediated the metasomatism that preceded Group I kimberlite eruptions in the southwestern Kaapvaal craton, and that their ‘cold and oxidized’ nature reflects their derivation from a deep subducting slab. To reconcile the temperature and oxygen fugacity discrepancy between inclusions in diamonds and xenoliths, we argue that xenoliths did not equilibrate during the last saline metasomatic event or kimberlite eruption. Thus the P-T-??O2 gradients they record express pre-existing lithospheric conditions that were likely established during the last major thermal event in the Kaapvaal craton (i.e. the Karoo magmatism at ca. 180 Ma).
Abstract: Olivine phenocryst chemistry is a useful tracer of mantle source lithology as olivine is typically the first mineral to crystallize in a range of mafic to alkaline magma types and contains geochemical information about the primary parent magma composition. It is particularly useful in discriminating between pyroxenite (i.e.,recycled crustal component) and peridotite mantle source lithologies. Radiogenic isotope studies of HIMU basalts have shown the important role of a recycled crustal component in the source. However, olivine chemistry of HIMU basalts suggests a dominantly peridotitic mantle source with a subduction-derived metasomatic carbonate component. To further investigate how olivine chemistry can be used to understand the source of HIMU magmas, I present major and trace element data for olivine megacrysts related to the 89?Ma Cr-poor megacryst suite from the Monastery kimberlite (South Africa), which have previously been interpreted to crystallize at high P-T conditions of ~1400?°C and ~5?GPa from a magma sourced from a HIMU reservoir. Olivine megacrysts have high-Ni concentrations at a given Fo (forsterite) content, overlapping ocean island basalts (OIB) interpreted to have formed from pyroxenite-dominated sources but are distinct from typical olivine in HIMU basalts. However, they have low 100*Mn/Fe (0.8-1.1) and no correlation is observed between Ni and trace elements indicative of recycled components such as Co, Li, or Zn. The olivine megacryst chemistry is similar to that of aillikite olivine interpreted to be controlled by phlogopite in the source rather than pyroxenite. Comparison with olivine chemistry from orangeites/Group II kimberlites (sourced from phlogopite-rich mantle lithologies) supports a phlogopite controlon low 100*Mn/Fe in olivine. Further comparison with olivine phenocryst chemistry of HIMU melilitites (76-58?Ma) in southern Africa suggests a mineralogically heterogeneous HIMU reservoir formed by metasomatic modification of the lithospheric mantle in southern Africa. Thus, olivine megacryst chemistry supports interpretations for the recycled component of the HIMU reservoir as mineralogically complex metasomatic lithologies formed by the infiltration of subduction-derived melts into the base of the lithospheric mantle. In addition to carbonate-richHIMU mantle lithologies in southern Africa and worldwide, Monastery kimberlite olivine megacrysts and olivine in melilitites suggest that a phlogopite-richHIMU lithology is present in southern Africa. An important question arising from this study is in reconciling the homogenous isotopic ratios of HIMU basalts worldwide with an apparent heterogeneous lithological source indicated by olivine chemistry.
Abstract: The flux of elements into Earth's sub-continental lithospheric mantle is facilitated by the passage of small-fraction melts that either crystallise new phases or react with pre-existing minerals.Metasomatised peridotite records the end product of this exchange but rarely captures the process in the act due to subsolidus re-equilibration. We present the results of a systematic investigation of a metasomatic melt channel preserved in a mantle peridotite from the Late Cretaceous Bultfontein kimberlite (Kaapvaal craton) that shows rare direct evidence of the melt-rock reaction processes. We show that the metasomatic proto-kimberlite melt underwent variable crystallisation of clinopyroxene, sulfides, phlogopite, spinel and zircon together with interaction and diffusive exchange with the surrounding olivine-rich mantle. Element profiles across large olivine porphyroclasts (Fo88) show significant core-to-rim variations in Ni (NiO?=?0.18-0.32?wt%) and Cr (Cr?=?35-60?ppm), while concentrations of all other elements (e.g. Mg, Fe, Mn, Co, V)are remarkably homogeneous. Electron backscatter diffraction analysis shows that the disequilibrium of Ni and Cr is greatest where the crystal contains large components of the [100] and [010] axes. The disequilibrium is preserved in certain orientations because diffusion of Ni and Cr in olivine is more anisotropic than Fe-Mg and Mn, and slower in the [100] and [010] directions. We present the first observations of Ni and Cr decoupling from other elements in mantle olivine and suggest that this is a consequence of: (i)changing mineral-melt concentration gradients associated with the reactive percolation of a precursory kimberlite melt; and (ii) late-stage sulfide and spinel precipitation. We use the diffusion limited re-equilibration of Ni in olivine to quantify the timing of metasomatism prior to xenolith entrainment by the host kimberlite. Our modelling indicates that reactive percolation occurred on the order of 103-105?years prior to entrainment; this provides an additional line of support for the hypothesis that a period of metasomatism by proto-kimberlite melts precedes the final kimberlite ascent to the surface. The broader implication of our finding of variable rates of minor element diffusion in natural olivine is that it highlights the importance of anisotropy and the impact of changing local concentration gradients during subsolidus re-equilibration.
Mineralogy and Petrology, doi:10.1007/ s00710-018-0568-9 15p.
Africa, South Africa
deposit - Group I, orangeites Group II
Abstract: The West Coast of Namaqualand in South Africa hosts extensive detrital diamond deposits, but considerable debate exists as to the provenance of these diamonds. Some researchers have suggested derivation of the diamonds from Cretaceous-Jurassic kimberlites (also termed Group I kimberlites) and orangeites (also termed Group II kimberlites) located on the Kaapvaal Craton. However, others favour erosion of diamonds from the ca.300 Ma Dwyka Group sediments, with older, pre-Karoo kimberlites being the original source(s). Previous work has demonstrated that 40Ar/39Ar analyses of clinopyroxene inclusions, extracted from diamonds, yield ages approaching the time(s) of source kimberlite emplacement, which can be used to constrain the provenance of placer diamond deposits. In the current study, 40Ar/39Ar analyses were conducted on clinopyroxene inclusions from two similar batches of Namaqualand detrital diamonds, yielding (maximum) ages ranging from 117.5?±?43.6 Ma to 3684?±?191 Ma (2s) and 120.6?±?15.4 Ma to 688.8?±?4.9 Ma (2s), respectively. The vast majority of inclusions (88%) produced ages younger than 500 Ma, indicating that most Namaqualand diamonds originated from Cretaceous-Jurassic kimberlites/orangeites, with few, if any, derived from the Dwyka tillites. The provenance of the Namaqualand diamonds from ca.115-200 Ma orangeites is consistent with Late Cretaceous paleo-drainage reconstructions, as these localities could have been sampled by the ‘paleo-Karoo’ River and transported to the West Coast via an outlet close to the current Olifants River mouth. At ca.90 Ma, this drainage system appears to have been captured by the ‘paleo-Kalahari’ River, a precursor to the modern Orange River system. This latter drainage is considered to have transported diamonds eroded from both ca.80-90 Ma kimberlites and ca.115-200 Ma orangeites to the West Coast, which were subsequently reworked along the Namibian coast, forming additional placer deposits.
History of Photography, Vol. 42, 1, pp. 4-24. doi.org/10.1080/ 03087298.2018. 1429095
Africa, South Africa
deposit - Kimberley
Abstract: In the mid 1880s a little-known photographer named Robert Harris produced a series of albumen prints showing the stages of body searching that black labourers in De Beers diamond mines were obliged to undergo by state ordinance enacted in 1883. The original photographs surfaced briefly in the saleroom in 2007 but have since disappeared. Two sets of copies survive. Bearing in mind the history of documentary photography in South Africa, this article examines the historical and textual significance of this series of photographs in the context of the history of mining and discusses the imperatives and ethics of locating, researching, and publishing controversial imagery in the Internet age.
The Southern African Institute of Mining and Metallurgy Diamonds - from source to use 2013, 9p. Pdf researchgate
Africa, Angola, South Africa
deposit - Mulepe, Voorspoed
Abstract: Construction of geological models for kimberlites has historically largely been based on visual volcanic textures and features, with chemical data only produced on an ad-hoc basis depending on the level of perceived complexity observed in the geological data. The focus of this manuscript is a high-level mineral resource management view of the impact which the initial absence of proper chemical data had on two kimberlite resource models as well as the increasing magnitude of the problem caused by the lack of chemical data once the resource estimation process commenced. The impact of the absence of chemical data on projects where micro-diamond estimation techniques are employed is also discussed. Metallurgical parameters have historically not been incorporated into kimberlite resource models, but recent work at De Beers Group Services has shown that geostatistical quantification of the DMS (Dense Media Separator) yield is useful for mine planning purposes, and will add value in the understanding of the kimberlite emplacement process. A case study is presented where a geostatistical analysis and conditional simulation was performed on the DMS yield in a kimberlite at a local block scale. These data were used to identify mining blocks where the DMS yield would exceed the capability of the treatment plant.
Abstract: Geologists have a new window onto the early Earth: zircon crystals from South Africa that could be as much as 4.1 billion years old. Ancient crystals of zircon - a durable mineral found in rock that has been squeezed and heated - from Western Australia have revealed some of the planet’s early secrets, such as clues to the chemistry of its primordial crust. But researchers have had little in the way of other records for this period of Earth’s infancy. Now, Benjamin Byerly at Louisiana State University in Baton Rouge and his colleagues report their discovery of a second rich trove of zircons. The crystals lie east of Pretoria, in a rock formation known as the Barberton greenstone belt. The African zircons are important because they have been subject to less heating and squeezing than the Australian samples. As a result, the African crystals may have richer stories to tell about the chemistry of Earth’s early years.
Abstract: The question of whether high-grade metamorphism and crustal melting in the early Archaean were associated with modern-style plate tectonics is a major issue in unravelling early Earth crustal evolution, and the eastern Kaapvaal craton has featured prominently in this debate. We discuss a major ca. 3.2?Ga tectono-magmatic-metamorphic event in the Ancient Gneiss Complex (AGC) of Swaziland, a multiply deformed medium- to high-grade terrane in the eastern Kaapvaal craton consisting of 3.66-3.20?Ga granitoid gneisses and infolded greenstone remnants, metasedimentary assemblages and mafic dykes. We report on a 3.2?Ga granulite-facies assemblage in a metagabbro of the AGC of central Swaziland and relate this to a major thermo-magmatic event that not only affected the AGC but also the neighbouring Barberton granitoid-greenstone terrane. Some previous models have related the 3.2?Ga event in the eastern Kaapvaal craton to subduction processes, but we see no evidence for long, narrow belts and metamorphic facies changes reflecting lithospheric suture zones, and there is no unidirectional asymmetry in the thermal structure across the entire region from Swaziland to the southern Barberton granite-greenstone terrane as is typical of Phanerozoic and Proterozoic belts. Instead, we consider an underplating event at ca. 3.2?Ga, giving rise to melting in the lower crust and mixing with mantle-derived under- and intraplated mafic magma to generate the voluminous granitoid assemblages now observed in the AGC and the southern Barberton terrane. This is compatible with large-scale crustal reworking during a major thermo-magmatic event and the apparent lack of a mafic lower crust in the Kaapvaal craton as shown by seismic data.
Journal of Geophysical Research: Solid Earth, doi: 10.1029/2018JB016012
Africa, South Africa
diamond inclusions
Abstract: Here we report the first results from elastic geobarometry applied to a kyanite inclusion entrapped within an eclogitic diamond (from Voorspoed mine, South Africa) using micro?Raman and Fourier transform infrared spectroscopy, electron microprobe analysis, ab initio calculations, and finite element modeling. Application of elastic geobarometry to very elastically anisotropic kyanite inclusions is challenging, as current models do not allow for elastic anisotropy. In order to minimize the effects of anisotropy, we have explored the effects of deviatoric stress on Raman modes via ab initio density functional theory. The results allowed us to select the Raman mode (at ca. 638 cm?1) that is the least sensitive to deviatoric stress. The shift of this band in the inclusion while still trapped within the diamond relative to the inclusion in air (once liberated) was used under hydrostatic approximation to determine a residual pressure on the inclusion of 0.184 ± 0.045 GPa and an entrapment pressure of 5.2 ± 0.3 GPa (~160 km depth) for an FTIR N?aggregation residence temperature of 1119 ± 50 °C. This is the first geothermobarometric determination for a diamond from the Voorspoed kimberlite. It overlaps with P-T estimates obtained by traditional chemical geobarometry for diamonds from other kimberlites from the Kaapvaal craton, suggesting that the hydrostatic approximation does not introduce significant errors in the geobarometric evaluation. Our protocol of Raman peak selection can be used for geobarometry of further kyanite?bearing diamonds and may provide a guide for more robust geobarometry of other types of mineral inclusions in diamonds, both eclogitic and peridotitic.
Earth and Planetary Science Letters, Vol. 503, pp. 108-117.
Africa, South Africa, Zimbabwe
geophysics - seismic
Abstract: The depths of the 410 km (d410) and 660 km (d660) discontinuities beneath southern Africa, which is presumably underlain by the lower-mantle African Superswell, are imaged in 1? radius consecutive circular bins using over 6400 P-to-S receiver functions (RFs) recorded by 130 seismic stations over a 27 yr period. When the IASP91 standard Earth model is utilized for moveout correction and time-depth conversion, a normal mantle transition zone (MTZ) thickness of 246 ± 7 km is observed, suggesting that the Superswell has no discernible effect on mantle transition zone temperature. Based on the negligible disparity of the mean MTZ thicknesses between on (246 ± 6 km) and off (246 ± 8 km) cratonic regions, we conclude that the deep Archean cratonic keels possess limited influence on MTZ thermal structure. The apparently shallower-than-normal MTZ discontinuities and the parallelism between the d410 and d660 are mostly the results of upper mantle high wave speed anomalies probably corresponding to a thick lithosphere with a mean thickness of about 245 km beneath the Kaapvaal and 215 km beneath the Zimbabwe cratons. In contradiction to conclusions from some of the previous studies, the resulting spatial distribution of the stacking amplitudes of the P-to-S converted phases at the discontinuities is inconsistent with the presence of an excessive amount of water in the MTZ and atop the d410.
Abstract: The Benfontein kimberlite is a renowned example of a sill complex and provides an excellent opportunity to examine the emplacement and evolution of intrusive kimberlite magmas. We have undertaken a detailed petrographic and melt inclusion study of the Benfontein Upper, Middle and Lower sills. These sills range in thickness from 0.25 to 5?m. New perovskite and baddeleyite U/Pb dating produced ages of 85.7?±?4.4?Ma and 86.5?±?2.6?Ma, respectively, which are consistent with previous age determinations and indicate emplacement coeval with other kimberlites of the Kimberley cluster. The Benfontein sills are characterised by large variations in texture (e.g., layering) and mineral modal abundance between different sill levels and within individual samples. The Lower Sill is characterised by carbonate-rich diapirs, which intrude into oxide-rich layers from underlying carbonate-rich levels. The general paucity of xenogenic mantle material in the Benfontein sills is attributed to its separation from the host magma during flow differentiation during lateral spreading. The low viscosity is likely responsible for non-explosive emplacement of the Benfontein sills, while the rhythmic layering is attributed to multiple magma injections. The Benfontein sills are marked by the excellent preservation of olivine and groundmass mineralogy, which is composed of monticellite, spinel, perovskite, baddeleyite, ilmenite, apatite, calcite, dolomite along with secondary serpentine and glagolevite [NaMg6[Si3AlO10](OH,O)8•H2O]. This is the first time glagolevite is reported in kimberlites. Groundmass spinel exhibits atoll-textures and is composed of a magnesian ulvöspinel magnetite (MUM) or chromite core, surrounded by occasional pleonaste and a rim of Mg-Al-magnetite. We suggest that pleonaste crystallised as a magmatic phase, but was resorbed back into the residual host melt and/or removed by alteration. Analyses of secondary inclusions in olivine and primary inclusions in monticellite, spinel, perovskite, apatite and interstitial calcite are largely composed of Ca-Mg carbonates and, to a lesser extent, alkali-carbonates and other phases. These inclusions probably represent the entrapment of variably differentiated parental kimberlite melts, which became progressively more enriched in carbonate, alkalis, halogens and sulphur during crystal fractionation. Carbonate-rich diapirs from the Lower Sill contain more exotic phase assemblages (e.g., Ba-Fe titanate, barite, ancylite, pyrochlore), which probably result from the extreme differentiation of residual kimberlite melts followed by physical separation and isolation from the parental carbonate-rich magma. It is likely that any alkali or halogen rich minerals crystallising in the groundmass were removed from the groundmass during syn?/post-magmatic alteration, or in the case of Na, remobilised to form secondary glagolevite. The Benfontein sill complex therefore provides a unique example of how the composition of kimberlites may be modified after magma emplacement in the upper crust.
2018 Yellowknife Geoscience Forum , p. 91-92. abstract
Africa, South Africa
deposit - Roberts Victor
Abstract: It is well known that mechanical disaggregation, such as jaw crushing, can cause irreversible damage to valuable gemstones hosted in crystalline rocks. The SELFRAG Lab device uses electrical pulses at high voltages - typically between 150 and 200 kV - to separate material into individual grains along natural boundaries. The purpose of this research is to assess the viability of the SELFRAG as a tool to disaggregate diamond-bearing eclogites, and to assess if this method preserves grains that would otherwise be damaged through mechanical disaggregation. In order to test the applicability of the SELFRAG to diamond recovery from mechanically strong diamond-bearing lithologies, we studied its effects on a diamondiferous eclogite, RV09, from Roberts Victor mine. The Roberts Victor mine is located in South Africa and is renowned for its unusually high abundance of mantle-derived eclogite xenoliths1. Before the eclogite was disaggregated, we bisected the sample and used a CT scan to determine its constituent minerals and the spatial distribution of diamond. One half of the sample was then placed into the SELFRAG, where it was subjected to ~100 shots of 200 kV electrical discharges that segregated the sample into individual grains of similar sizes. The other half was jaw crushed, using a steel jaw crusher which produced non-uniform composite grains and abundant fine material. The varying sizes and aggregate pieces made it difficult to pick diamonds, and after no diamonds were found, the jaw-crushed portion underwent further disaggregation in the SELFRAG. After exerting the same time and effort picking through both portions of the RV09 sample, ten diamonds were recovered from the electronically disaggregated portion, while no diamonds were found in the conventionally disaggregated sample. The diamonds released from the SELFRAG were then imaged with a scanning electron microscope (SEM) to determine the extent to which the diamonds were damaged. Most of the released diamonds showed no evidence of breakage, but a few showed signs of damage that may have occurred prior to kimberlite eruption. The dramatic disparity between the number of diamonds recovered with the SELFRAG and the lack of diamonds in the jaw crushed portion indicates that electrical disaggregation is a superior method compared to the conventional mechanical comminution technique. There are little to no signs of breakage in the SELFRAG-liberated diamonds, whereas, the damage caused by jaw crushing was extensive enough to produce small fragments not readily visible via optical microscopy. The SELFRAG is a promising alternative to conventional disaggregation and offers a practical solution for lessening damage to valuable stones in rocks such as eclogites and kimberlites.
Abstract: A detailed electron microprobe study has been carried out on the compositional variations of mica and apatite from carbonatites, phoscorites and associated pyroxenites (and fenites) of the Loolekop deposit, Palabora Carbonatite Complex (South Africa). Mica in pyroxenites and fenites is Mg-rich biotite, whilst micas in carbonatites and phoscorites are compositionally diverse including phlogopite, Ba-rich phlogopite (up to 30% kinoshitalite component), IVAl-rich phlogopite (up to 30% eastonite component) and tetraferriphlogopite. The various types of phlogopites are interpreted as orthomagmatic phases, whereas tetraferriphlogopite precipitation was a late-magmatic to hydrothermal process that additionally introduced REE into the system. Orthomagmatic apatite is generally REE- and Sr-poor fluorapatite and does not show large compositional differences between rock types. Apatite associated with the late-stage tetraferriphlogopite mineralization reaches higher levels of REE (up to 4.9?wt%), Si (up to 1.5?wt% SiO2), Sr (up to 2.6?wt% SrO) and Na (up to 1.0?wt% Na2O). The compositional variation of micas and apatites, which is affiliated with distinct rock types, reflects the multi-stage evolution of the Loolekop deposit and provides detailed insight into the relationships of the carbonatite-phoscorite assemblage. The obtained data support the separation of phoscorite and carbonatite by immiscibility from a common parental magma, which may happen due to a decrease of temperature and/or pressure during the ascent of the magma. This results in a density contrast between the carbonatitic and phoscoritic components that will lead to descending phoscorite accumulations at the outer zones of the magma channel and a jet-like ascent (further promoted by its extremely low viscosity) of the carbonatite magma. The genetic model deduced here explains the peculiar association of carbonatites, phoscorites and silicate rocks in many alkaline complexes worldwide.
Abstract: The flux of elements into Earth’s sub-continental lithospheric mantle is facilitated by the passage of small-fraction melts that either crystallise new phases or react with pre-existing minerals. Metasomatised peridotite records the end product of this exchange but rarely captures the process in the act due to subsolidus re-equilibration. We present the results of a systematic investigation of a metasomatic melt channel preserved in a mantle peridotite from the Late Cretaceous Bultfontein kimberlite (Kaapvaal craton) that shows rare direct evidence of the melt-rock reaction processes. We show that the metasomatic proto-kimberlite melt underwent variable crystallisation of clinopyroxene, sulfides, phlogopite, spinel and zircon together with interaction and diffusive exchange with the surrounding olivine-rich mantle. Element profiles across large olivine porphyroclasts (Fo88) show significant core-to-rim variations in Ni (NiO = 0.18-0.32 wt.%) and Cr (Cr = 35-60 ppm), while concentrations of all other elements (e.g. Mg, Fe, Mn, Co, V) are remarkably homogeneous. Electron backscatter diffraction analysis shows that the disequilibrium of Ni and Cr is greatest where the crystal contains large components of the [100] and [010] axes. The disequilibrium is preserved in certain orientations because diffusion of Ni and Cr in olivine is more anisotropic than Fe-Mg and Mn, and slower in the [100] and [010] directions. We present the first observations of Ni and Cr decoupling from other elements in mantle olivine and suggest that this is a consequence of: (i) changing mineral-melt concentration gradients associated with the reactive percolation of a precursory kimberlite melt; and (ii) late-stage sulfide and spinel precipitation. We use the diffusion limited re-equilibration of Ni in olivine to quantify the timing of metasomatism prior to xenolith entrainment by the host kimberlite. Our modelling indicates that reactive percolation occurred on the order of 103-105 years prior to entrainment; this provides an additional line of support for the hypothesis that a period of metasomatism by proto-kimberlite melts precedes the final kimberlite ascent to the surface. The broader implication of our finding of variable rates of minor element diffusion in natural olivine is that it highlights the importance of anisotropy and the impact of changing local concentration gradients during subsolidus re-equilibration.
Canada, Ontario, Attawapiskat, Africa, South Africa
deposit - Victor, Finsch, Newlands
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. “Planed” and “ribbed” trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Abstract: A study of the morphology, mineral inclusions, nitrogen content, and nitrogen aggregation state of diamonds from the Voorspoed kimberlite, was conducted. The diamonds are characterised by a highly unusual inclusion mineral paragenesis dominated by eclogitic and transitional websteritic-lherzolitic inclusions along with related websteritic inclusions, while a comparatively minor harzburgitic diamond inclusion suite account for the remainder. This differs substantially from many of the diamond populations in kimberlites on the Kaapvaal Craton where a harzburgitic inclusion paragenesis predominates. Only in the case of the Orapa kimberlite in Botswana has a similar diamond inclusion suite been encountered before, although in that instance an eclogitic and websteritic inclusion suite predominate. Calculated garnet-clinopyroxene equilibration temperatures, at an assumed pressure of 50?kbar, range from 1040 °C to 1296?°C. Temperatures of 1114?°C to 1348?°C, at 50?kbar, are calculated for lamellar orthopyroxene-clinopyroxene intergrowths. ‘Reconstituted’ pyroxenes mathematically reconstructed from the lamellar orthopyroxene-clinopyroxene intergrowths produce temperatures of 1238?°C to 1416?°C, suggesting that the lithosphere cooled by at least 100?°C after diamond crystallisation. Nitrogen contents and nitrogen aggregation states of whole diamonds range from below the detection limit (~10?ppm) to 1442 atomic ppm (average 167 atomic ppm), and up to 97% of the highly aggregated ‘B' component (average 65%), respectively. The elevated aggregation state of the nitrogen in the diamonds from Voorspoed, coupled with a high level of platelet degradation in many of the diamonds analysed, relative to a world-wide database, is unusual, but broadly comparable to diamonds from kimberlites occurring in craton margin settings, such as Argyle and Venetia. Diamond inclusion thermobarometry, as well as the elevated nitrogen aggregation states of the diamonds (coupled with the evidence for platelet degradation in the diamonds) are indicative of a diamond crystallisation event associated with a transient thermal pulse, as well as associated deformation of the mantle containing the diamonds. The websteritic and the transitional websteritic-lherzolitic mantle source rocks of the Voorspoed diamonds likely formed through melt infiltration into mantle peridotite, possibly in the reaction envelope surrounding an ascending mantle plume. In order to account for the unusually low abundance of harzburgitic diamonds at Voorspoed, it is postulated that a primary, pre-existing suite of harzburgitic diamonds which have crystallised in the Mesoarchaean, was destroyed through heating and oxidation during the passage of magmas associated with the Ventersdorp large igneous province at 2.72?Ga, and which was subsequently followed by the crystallisation of a younger eclogitic and transitional websteritic-lherzolitic suite of diamonds.
South African Journal of Geology, Vol. 121, pp. 227-236.
Africa, South Africa
geomorphology
Abstract: Rocky reaches of the southeast African coastline are characterized mainly by log-spiral and headland-bound bays. Extensive fieldwork was carried out to investigate both documented and new exposures of Cretaceous beds on the southern KwaZulu-Natal and upper Eastern Cape (Transkei) coasts. Our results suggest that geological inheritance plays an important role in the contemporary rocky coast geomorphology. We offer evidence that post-Gondwana break-up mass flow channels play an important role in the present southeast African coastline morphology. Mass flow channels contain fills of incompetent Cretaceous rocks which are being preferentially eroded by prevailing marine and fluvial processes to form headland-bound embayment landforms. This study has identified an important geomorphic process for the development of the current southeast African coastline.
Gems & Gemology, Sixth International Gemological Symposium Vol. 54, 3, 1p. Abstract p. 274.
Africa, South Africa, Angola
deposit - Cullinan, Lulo
Abstract: Many of the world’s largest and most valuable gem diamonds exhibit an unusual set of physical characteristics. For example, in addition to their conspicuously low nitrogen concentrations, diamonds such as the 3,106 ct Cullinan (type IIa) and the Hope (type IIb, boron bearing) tend to have very few or no inclusions, and in their rough state they are found as irregular shapes rather than as sharp octahedral crystals. It has long been suspected that type IIa and IIb diamonds form in a different way than most other diamonds. Over the past two years, systematic investigation of both type IIa and IIb diamonds at GIA has revealed that they sometimes contain rare inclusions from unique geological origins. Examination of more than 130 inclusion-bearing samples has established recurring sets of inclusions that clearly show many of these diamonds originate in the sublithospheric mantle, much deeper in the earth than more common diamonds from the cratonic lithosphere. We now recognize that type IIa diamonds, or more specifically, diamonds with characteristics akin to the historic Cullinan diamond (dubbed CLIPPIR diamonds), are distinguished by the occurrence of ironrich metallic inclusions. Less frequently, CLIPPIR diamonds also contain inclusions of majoritic garnet and former CaSiO3perovskite that constrain the depth of formation to within 360–750 km. The inclusions suggest that CLIPPIR diamonds belong to a unique paragenesis with an intimate link to metallic iron in the deep mantle (Smith et al., 2016, 2017). Similarly, findings from type IIb diamonds also place them in a “superdeep” sublithospheric mantle setting, with inclusions of former CaSiO3 perovskite and other high-pressure minerals, although the iron-rich metallic inclusions are generally absent (Smith et al., 2018). Altogether, these findings show that high-quality type II gem diamonds are predominantly sourced from the sublithospheric mantle, a surprising result that has refuted the notion that all superdeep diamonds are small and nongem quality. Valuable information about the composition and behavior of the deep mantle is cryptically recorded in these diamonds. CLIPPIR diamonds (figure 1) confirm that the deep mantle contains metallic iron, while type IIb diamonds suggest that boron and perhaps water can be carried from the earth’s surface down into the lower mantle by plate tectonic processes. In addition to being gemstones of great beauty, diamonds carry tremendous scientific value in their unique ability to convey information about the interior of our planet.
Abstract: The Benfontein kimberlite is a renowned example of a sill complex and provides an excellent opportunity to examine the emplacement and evolution of intrusive kimberlite magmas. We have undertaken a detailed petrographic and melt inclusion study of the Benfontein Upper, Middle and Lower sills. These sills range in thickness from 0.25 to 5?m. New perovskite and baddeleyite U/Pb dating produced ages of 85.7?±?4.4?Ma and 86.5?±?2.6?Ma, respectively, which are consistent with previous age determinations and indicate emplacement coeval with other kimberlites of the Kimberley cluster. The Benfontein sills are characterised by large variations in texture (e.g., layering) and mineral modal abundance between different sill levels and within individual samples. The Lower Sill is characterised by carbonate-rich diapirs, which intrude into oxide-rich layers from underlying carbonate-rich levels. The general paucity of xenogenic mantle material in the Benfontein sills is attributed to its separation from the host magma during flow differentiation during lateral spreading. The low viscosity is likely responsible for non-explosive emplacement of the Benfontein sills, while the rhythmic layering is attributed to multiple magma injections. The Benfontein sills are marked by the excellent preservation of olivine and groundmass mineralogy, which is composed of monticellite, spinel, perovskite, baddeleyite, ilmenite, apatite, calcite, dolomite along with secondary serpentine and glagolevite [NaMg6[Si3AlO10](OH,O)8•H2O]. This is the first time glagolevite is reported in kimberlites. Groundmass spinel exhibits atoll-textures and is composed of a magnesian ulvöspinel - magnetite (MUM) or chromite core, surrounded by occasional pleonaste and a rim of Mg-Al-magnetite. We suggest that pleonaste crystallised as a magmatic phase, but was resorbed back into the residual host melt and/or removed by alteration. Analyses of secondary inclusions in olivine and primary inclusions in monticellite, spinel, perovskite, apatite and interstitial calcite are largely composed of Ca-Mg carbonates and, to a lesser extent, alkali-carbonates and other phases. These inclusions probably represent the entrapment of variably differentiated parental kimberlite melts, which became progressively more enriched in carbonate, alkalis, halogens and sulphur during crystal fractionation. Carbonate-rich diapirs from the Lower Sill contain more exotic phase assemblages (e.g., Ba-Fe titanate, barite, ancylite, pyrochlore), which probably result from the extreme differentiation of residual kimberlite melts followed by physical separation and isolation from the parental carbonate-rich magma. It is likely that any alkali or halogen rich minerals crystallising in the groundmass were removed from the groundmass during syn?/post-magmatic alteration, or in the case of Na, remobilised to form secondary glagolevite. The Benfontein sill complex therefore provides a unique example of how the composition of kimberlites may be modified after magma emplacement in the upper crust.
Contributions to Mineralogy and Petrology, Vol. 174, 8 22p.
Africa, South Africa, Russia, Canada, Northwest Territories
deposit - Bultfontein, Roberts Victor, Udachnaya-East, Obnazhennaya, Vtorogodnitsa, Koala, Leslie
Abstract: Djerfisherite (K6(Fe,Ni,Cu)25S26Cl) occurs as an accessory phase in the groundmass of many kimberlites, kimberlite-hosted mantle xenoliths, and as a daughter inclusion phase in diamonds and kimberlitic minerals. Djerfisherite typically occurs as replacement of pre-existing Fe-Ni-Cu sulphides (i.e. pyrrhotite, pentlandite and chalcopyrite), but can also occur as individual grains, or as poikilitic phase in the groundmass of kimberlites. In this study, we present new constraints on the origin and genesis of djerfisherite in kimberlites and their entrained xenoliths. Djerfisherite has extremely heterogeneous compositions in terms of Fe, Ni and Cu ratios. However, there appears to be no distinct compositional range of djerfisherite indicative of a particular setting (i.e. kimberlites, xenoliths or diamonds), rather this compositional diversity reflects the composition of the host kimberlite melt and/or interacting metasomatic medium. In addition, djerfisherite may contain K and Cl contents less than the ideal formula unit. Raman spectroscopy and electron backscatter diffraction (EBSD) revealed that these K-Cl poor sulphides still maintain the same djerfisherite crystal structure. Two potential mechanisms for djerfisherite formation are considered: (1) replacement of pre-existing Fe-Ni-Cu sulphides by djerfisherite, which is attributed to precursor sulphides reacting with metasomatic K-Cl bearing melts/fluids in the mantle or the transporting kimberlite melt; (2) direct crystallisation of djerfisherite from the kimberlite melt in groundmass or due to kimberlite melt infiltration into xenoliths. The occurrence of djerfisherite in kimberlites and its mantle cargo from localities worldwide provides strong evidence that the metasomatising/infiltrating kimberlite melt/fluid was enriched in K and Cl. We suggest that kimberlites originated from melts that were more enriched in alkalis and halogens relative to their whole-rock compositions.
Abstract: Strontium and Pb isotopic compositions of clinopyroxene (cpx) in selected samples from three well-characterised eclogite suites with oceanic crustal protoliths (Lace/Kaapvaal craton, Orapa/Zimbabwe craton and Koidu/West African craton) were acquired by high-precision isotope dilution thermal ionisation mass spectrometry (ID-TIMS) and in situ multicollector-laser ablation-inductively-coupled plasma mass spectrometry (MC-LA-ICPMS). The aims of this study are twofold: (1) assess their utility to obtain formation or resetting age constraints and identify elemental signatures that enhance the chances of successful age dating, and (2) to confirm the veracity and utility of results obtained by novel MC-LA-ICPMS techniques. Strontium-Pb isotope systematics of eclogitic cpx measured in this study are decoupled and may reflect addition of unsupported radiogenic Sr during seawater alteration or interaction with oceanic sediments in subduction mélanges, and/or disturbance due to mantle metasomatism, to which the more incompatible Pb is more susceptible. Despite a complex history, subsets of samples yield meaningful model dates. Clinopyroxene fractions from Lace with high Pb contents (3-6?ppm), unradiogenic Pb isotopic compositions (206Pb/204Pb?=?13.57-13.52) and low 238U/204Pb (1.0-1.5) give single-stage model Pb dates of 2.90-2.84?Ga. In contrast, samples from Orapa plot to the right of the Geochron and do not yield meaningful Pb model ages. However, these data do define secondary isochrons that can be modelled to yield minimum age constraints on major events affecting the cratonic lithosphere. Within the uncertainties, the resultant 2.18?±?0.45?Ga age obtained for Koidu eclogites reflect disturbance of the Pb isotope system due to subduction beneath the craton linked to the Eburnean orogeny, while they retained their unradiogenic 87Sr/86Sr (0.7016). Similarly, the age for samples from Orapa (2.20?±?0.54?Ga) is interpreted as an overprint age related to Palaeoproterozoic accretion at the western craton margin. Gabbroic eclogites (Eu/Eu*?>?1) with plagioclase-rich protoliths having low time-integrated Rb/Sr and U/Pb retain the least radiogenic Sr and, in part, Pb. High model ? (9.0 to 9.1) for several eclogites from Lace with elevated LREE, Th and Pb abundances reflects ca. 3.0?Ga addition of a sedimentary component, possibly derived from reworking of a high-? basaltic protocrust, as observed on other cratons. We suggest that sample targeting can be usefully guided by fast-throughput in situ LA-ICPMS techniques, which largely yield results identical to ID-TIMS, albeit at lower precision, and which can further help identify kimberlite contamination in the mineral separates used for solution work.
A geochemical and Nd, Sr and stable Ca isotopic study of carbonatites and associated silicate rocks from the ~65 Ma old Ambadongar carbonatite complex and the Phenai Mata igneous complex, Gujarat, India: implications for crustal contamination, carbonate r
Earth and Planetary Science Letters, Vol. 506, pp. 15-26.
Africa, South Africa
deposit - Newlands, Kimberley, Bultfontein
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) and PIC (Phlogopite-Ilmenite-Clinopyroxene) rocks occur as mantle-derived xenoliths in kimberlites and other alkaline volcanic rocks. Both rock types are alkaline and ultramafic in composition. The H2O and alkali metal enrichments in MARID and PIC rocks, reflected in abundant phlogopite, have been suggested to be caused by extreme mantle metasomatism. Radiogenic (Sr-Nd-Hf-Pb) isotope and trace element compositions for mineral separates from MARID (clinopyroxene and amphibole) and PIC (clinopyroxene only) samples derived from Cretaceous kimberlites (Kimberley) and orangeites (Newlands) from South Africa are used here to examine the source(s) of mantle metasomatism. PIC clinopyroxene is relatively homogeneous, with narrow ranges in initial isotopic composition (calculated to the emplacement age of the host Bultfontein kimberlite; 87Sr/86Sri: 0.7037-0.7041; ?Ndi: +3.0 to +3.6; ?Hfi: +2.2 to +2.5; 206Pb/204Pbi: 19.72-19.94) similar to kimberlite values. This is consistent with PIC rocks representing peridotites modified by intense metasomatic interaction with kimberlite melts. The MARID clinopyroxene and amphibole separates () studied here display broader ranges in isotope composition (e.g., 87Sr/86Sri: 0.705-0.711; ?Ndi: ?11.0 to ?1.0; ?Hfi: ?17.9 to ?8.5; 206Pb/204Pbi: 17.33-18.72) than observed in previous studies of MARID rocks. The Nd-Hf isotope compositions of kimberlite-derived MARID samples fall below the mantle array (??Hfi between ?13.0 and ?2.4), a feature reported widely for kimberlites and other alkaline magmas. We propose that such displacements in MARID minerals result from metasomatic alteration of an initial “enriched mantle” MARID composition (i.e., 87Sr/86Sri = 0.711; ?Ndi = ?11.0; ?Hfi = ?17.9; and 206Pb/204Pbi = 17.3) by the entraining kimberlite magma (87Sr/86Sr; ?Nd; ?Hf; 206Pb/204Pb). A model simulating the flow of kimberlite magma through a mantle column, thereby gradually equilibrating the isotopic and chemical compositions of the MARID wall-rock with those of the kimberlite magma, broadly reproduces the Sr-Nd-Hf-Pb isotope compositions of the MARID minerals analysed here. This model also suggests that assimilation of MARID components could be responsible for negative ??Hfi values in kimberlites. The isotopic composition of the inferred initial MARID end-member, with high 87Sr/86Sr and low ?Nd, ?Hf, and 206Pb/204Pb, resembles those found in orangeites, supporting previous inferences of a genetic link between MARID-veined mantle and orangeites. The metasomatic agent that produced such compositions in MARID rocks must be more extreme than the EM-II mantle component and may relate to recycled material that experienced long-term storage in the lithospheric mantle.
Abstract: The oxidation state of iron in Earth’s mantle is well known to depths of approximately 200?km, but has not been characterized in samples from the lowermost upper mantle (200-410?km depth) or the transition zone (410-660?km depth). Natural samples from the deep (>200?km) mantle are extremely rare, and are usually only found as inclusions in diamonds. Here we use synchrotron Mössbauer source spectroscopy complemented by single-crystal X-ray diffraction to measure the oxidation state of Fe in inclusions of ultra-high pressure majoritic garnet in diamond. The garnets show a pronounced increase in oxidation state with depth, with Fe3+/(Fe3++ Fe2+) increasing from 0.08 at approximately 240?km depth to 0.30 at approximately 500?km depth. The latter majorites, which come from pyroxenitic bulk compositions, are twice as rich in Fe3+ as the most oxidized garnets from the shallow mantle. Corresponding oxygen fugacities are above the upper stability limit of Fe metal. This implies that the increase in oxidation state is unconnected to disproportionation of Fe2+ to Fe3+ plus Fe0. Instead, the Fe3+ increase with depth is consistent with the hypothesis that carbonated fluids or melts are the oxidizing agents responsible for the high Fe3+ contents of the inclusions.
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. "Planed" and "ribbed" trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Journal of the Southern African Insitiute of Mining and Metallurgy, Vol. 118, 8, pp. 845- 852.
Africa, South Africa
artisanal, alluvial
Abstract: The number of people involved in artisanal and small-scale mining (ASM) has grown quickly to about 40.5 million, compared to 7 million in industrial mining. Furthermore, the ASM sector is contributing significantly to global mineral supply and new opportunities are arising for ASM in an evolving mining ecosystem. Given this growth trend, it is important to ask whether ASM is likely to be successful in the mining of all types of orebodies. The history of early South African diamond mining suggests that the mining of a massive ore deposit by numerous artisanal and small-scale miners is likely to result in poor safety conditions as the depth of mining increases. Early photographs taken at the Kimberley mine showed a very uneven pit floor with leads-lags between the claims. This raises the question of why neighbouring miners did not ensure safer working conditions for each other. Two models described in the paper illustrate why there is likely to be a lack of cooperation and coordination between miners to address this and other safety-related problems. The dynamics of multiple claim holders mining next to one another at increasing depths are analysed, and it is shown that a consolidation of claims into a single firm per kimberlite pipe was required for improved planning, coordination, safety, efficiency, and sustainability.
Abstract: The Archean-Proterozoic transition was among the most important in geological history for it includes evidence of establishment of ‘modern-style’ plate tectonics, unprecedented paleoclimatic upheavals, and oxygenation of the atmosphere. The early Paleoproterozoic sedimentary record includes evidence of the world's first widespread glacial episodes, which have come to be known as the ‘Huronian Glacial Event’. None of these important changes coincides precisely with the accepted date of 2.5?Ga for the ‘boundary’ between the two great Precambrian eons. Rather, the geological record contains evidence of gradual transitions over many millions of years. For example the Archean sedimentary record in areas such as South Africa includes evidence of stable conditions (e.g. the Pongola Supergroup) that were not achieved in the Laurentian craton until much later during the Paleoproterozoic Era. The Pongola Supergroup in South Africa contains some of the world's oldest (c. 2.9?Ga) but locally developed glacial deposits. Many of these important changes are now considered to have been gradual and oscillatory in nature, including evidence of ‘whiffs of oxygen’ in Archean rocks, long before the Paleoproterozoic Great Oxidation Event. Oxidation of the oceans was also a long and extremely complex process, the details of which are still poorly understood. Glaciations near the beginning of the Paleoproterozoic Era have been considered by some to have been world-spanning ‘snowball Earth’ events. Repeated Huronian glaciations were probably brought about by weathering of Lauroscandia, the world's first ‘supercraton’, controlled by episodic rift-related uplifts during its disintegration. Among these glaciations only the third, represented by the Gowganda Formation and equivalents, was widespread throughout Lauroscandia. Because the two older glaciogenic units are known from only two locations in North America, their formation and preservation were probably controlled by local tectonic events. In like fashion, Paleoproterozoic glaciogenic units in South Africa and Western Australia appear to be local deposits from mountain glaciers formed during periods of tectonically generated (compressional?) uplift. The restricted distribution and diachronous nature of such tectonic events, and associated glaciogenic deposits, cast doubt on the viability of attempts at global correlations of individual Paleoproterozoic glaciogenic formations and on the existence of a Paleoproterozoic (or Neoproterozoic?) snowball Earth.
Contributions to Mineralogy and Petrology, Vol 174, https://doi.org/ 10.1007/s00410-019-1552-z
Africa, South Africa
deposit - Roberts Victor, Jagersfontein
Abstract: Mantle eclogites are commonly accepted as evidence for ancient altered subducted oceanic crust preserved in the subcontinental lithospheric mantle (SCLM), yet the mechanism and extent of crustal recycling in the Archaean remains poorly constrained. In this study, we focus on the petrological and geochemical characteristics of 58 eclogite xenoliths from the Roberts Victor and Jagersfontein kimberlites, South Africa. Non-metasomatized samples preserved in the cratonic root have variable textures and comprise bimineralic (garnet (gt)-omphacite (cpx)), as well as kyanite (ky)- and corundum (cor)-bearing eclogites. The bimineralic samples were derived from a high-Mg variety, corresponding to depths of ~ 100-180 km, and a low-Mg variety corresponding to depths of ~ 180-250 km. The high-Al (ky-, cor-bearing) eclogites originated from the lowermost part of the cratonic root, and have the lowest REE abundances, and the most pronounced positive Eu and Sr anomalies. On the basis of the strong positive correlation between gt and cpx ?18O values (r2 = 0.98), we argue that ?18O values are unaffected by mantle processes or exhumation. The cpx and gt are in oxygen isotope equilibrium over a wide range in ?18O values (e.g., 1.1-7.6‰ in garnet) with a bi-modal distribution (peaks at ~ 3.6 and ~ 6.4‰) with respect to mantle garnet values (5.1 ± 0.3‰). Reconstructed whole-rock major and trace element compositions (e.g., MgO variation with respect to Mg#, Al2O3, LREE/HREE) of bimineralic eclogites are consistent with their protolith being oceanic crust that crystallized from a picritic liquid, marked by variable degrees of partial melt extraction. Kyanite and corundum-bearing eclogites, however, have compositions consistent with a gabbroic and pyroxene-dominated protolith, respectively. The wide range in reconstructed whole-rock ?18O values is consistent with a broadly picritic to pyroxene-rich cumulative sequence of depleted oceanic crust, which underwent hydrothermal alteration at variable temperatures. The range in ?18O values extends significantly lower than that of present-day oceanic crust and Cretaceous ophiolites, and this might be due to a combination of lower ?18O values of seawater in the Archaean or a higher temperature of seawater-oceanic crust interaction.
Geochimica et Cosmochimica Acta, in press available 21p.
Africa, South Africa
deposit - Bultfontein
Abstract: Current understanding of the fate of subducted material (and related fluids) in the deep Earth can be improved by combining major and trace element geochemistry with stable isotopic compositions of mantle rocks or minerals. Limited isotopic fractionation during high temperature processes means that significant deviations from mantle-like isotope ratios in mantle rocks probably result from recycling of surficial material. To determine the effects and origins of mantle metasomatic fluids/melts, new ?15N and ?18O data have been collected for thirteen mantle xenoliths - harzburgites, wehrlites, lherzolites, and MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) rocks - from the Bultfontein kimberlite (Kimberley, South Africa), which show varying degrees of metasomatism. The ?18O values of olivine and orthopyroxene in phlogopite-free harzburgites match the mantle composition (?18Oolivine?=?+5.2?±?0.3‰; ?18Oorthopyroxene?=?+5.7?±?0.3‰; 2?s.d.), consistent with previous inferences that harzburgites were formed by interaction with ancient silica-rich melts unrelated to subduction processes. Wehrlite samples display mineral compositional characteristics (e.g., low La/Zr in clinopyroxene) resembling those of other products of kimberlite melt metasomatism, such as PIC (Phlogopite-Ilmenite-Clinopyroxene) rocks. The inferred interaction with kimberlite melts may be responsible for O isotopic disequilibrium between clinopyroxene and olivine (?18O?=?+0.2‰) in the wehrlites of this study. In contrast with broadly mantle-like ?18O values, the ?15N value of phlogopite in a wehrlite sample (+5.9‰) differs from the mantle composition (?15N?=??5?±?2‰). This unusual N isotopic composition in kimberlite-related mantle products might indicate that a recycled crustal component occurred in the source of the Kimberley kimberlites, or was assimilated during interaction with the lithospheric mantle. Similar major and trace element characteristics in clinopyroxene from phlogopite-lherzolite and MARID samples suggest metasomatism by fluids of similar composition. Lherzolite and MARID clinopyroxene ?18O values (as low as +4.4‰) extend below those reported in mantle peridotites (i.e. ?18Oclinopyroxene?=?+5.6?±?0.3‰; 2?s.d.), and strong negative correlations are found between mineral ?18O values and major element compositions (e.g., Na2O contents in clinopyroxene). Furthermore, phlogopite ?15N values (+4 to +7‰) in the studied lherzolite and MARID samples are higher than mantle values. Combined, the low ?18O-high ?15N isotopic signatures of MARID and lherzolite samples suggest progressive mantle metasomatism by a melt containing a recycled oceanic crust (eclogitic) component. This study demonstrates that progressive enrichment of the subcontinental lithospheric mantle may be inextricably linked to plate tectonics via recycling of subducted crustal material into the deep mantle.
Abstract: The evaluation of primary kimberlite compositions is hindered by significant melt modifications during ascent through the lithosphere by entrainment of xenolithic material, volatile degassing, and near surface alteration. Consequently, hypabyssal kimberlite emplaced in the upper crust may not provide a true reflection of the primary kimberlite magma. This contribution places new constraints on kimberlite melt composition by providing an assessment of quenched glass-rich polymineralic melt inclusions hosted in olivine megacrysts from the Monastery kimberlite, South Africa. Melt inclusions predominantly contain variable proportions of euhedral or skeletal grains of calcite, phlogopite, spinel, perovskite, serpentine, and fresh to devitrified glass. Estimates of the bulk compositions of melt inclusions, and the compositions of crystalline phases present therein, are compatible to those of hypabyssal kimberlites worldwide and show a volatile-rich (CO2?+?H2O ~10-17?wt%) carbonated silicate (SiO2 ~27-41?wt%) composition. The glass component has a Si-Mg-Fe-rich and largely CaO-, K2O- and TiO2-free major element composition and is REE-depleted. It also contains approximately 10?wt% H2O but is CO2?free. The glass represents a residual melt that existed after crystallization of the observed mineral assemblage. From some, but not all melt inclusions, apophyses radiate outwards. These fractures typically contain partially devitrified glass that is compositionally identical to the fresh residual glass within the melt inclusions, indicating fracture formation during decompression of the hosting megacryst and at a stage after the melt had evolved. These features are consistent with a trapping of the melt inclusions at high pressure, prior to kimberlite ascent to the surface, in the SCLM at a depth corresponding to 4.5-6?GPa. Textures and compositions of phases within the melt inclusions represent stages of the kimberlite melt and magma evolution. They provide evidence in support of high-pressure experimental studies suggesting a carbonated silicate primary melt rather than a carbonatite. Furthermore, the composition of fresh glass in the melt inclusions, which is compositionally similar to serpentine, suggests that much groundmass serpentine in hypabyssal kimberlites may have formed from similar silicate melt or devitrified glass.
Geochimica et Cosmochimica Acta, in press available, 19p.
Africa, South Africa, Canada, South America, Brazil
deposit - Lac de Gras, Paranaiba
Abstract: Kimberlites are the deepest melts produced on Earth that are erupted at the surface and can therefore provide unique insights into the composition and evolution of the mantle. Radiogenic isotopes provide ambiguous evidence for the occurrence of recycled crustal material in kimberlite sources. Oxygen isotopes can fractionate significantly only in the shallow crust, and thus represent a powerful tracer of subducted material in the sources of kimberlite. To constrain the oxygen isotope composition of kimberlite melts, we have examined olivine grains in eleven Cretaceous to Eocene archetypal kimberlites from southern Africa, Lac de Gras (Canada) and Alto Paranaiba (Brazil), which exhibit radiogenic isotope evidence for recycled crustal material in their sources including highly radiogenic Pb isotopes and Nd-Hf isotope compositions deviating below the mantle array. Olivine grains are commonly zoned between a mantle-derived xenocrystic core and one or more magmatic overgrowths, i.e. occasional internal zones, ubiquitous rims and rare rinds (moving outward from the core). The oxygen isotope composition of different olivine zones was determined in situ within separated olivine grains by secondary ion mass spectrometry (SIMS) after point selection using back-scattered electron (BSE) images combined with major and minor element analyses. With the exception of a few cores, the ?18O values of different olivine zones do not deviate from typical mantle olivine values of 5.18?±?0.28‰ (Mattey et al., 1994). There are no correlations between oxygen isotopes and major/minor element compositions for internal zones and rims from individual localities or in the entire dataset. This indicates that the oxygen isotope composition of kimberlite melts is not affected by melt differentiation to the point of olivine rim crystallisation. However, olivine rinds from the Koala kimberlite (Canada) display an inverse correlation between ?18O and Mn-Ca concentrations, with ?18O values extending below the mantle range, which is probably due to carbonate fractionation, CO2 degassing and/or assimilation of serpentine-rich material after kimberlite emplacement in the upper crust. The mantle-like ?18O composition of olivine internal zones and rims suggests that assimilation of mantle material and liberation of a CO2-rich phase during ascent in the mantle do not significantly modify the original ?18O signature of kimberlite melts. Modelling of oxygen isotope fractionation shows that up to 15 wt% of CO2 can be lost by kimberlites en route to the upper crust. Our results combined with mass balance calculations indicate that only a limited amount (<5-10 wt%) of recycled crustal material could occur in the source of kimberlites from southern Africa, Lac de Gras and Alto Paranaiba, or that the recycled material had an oxygen isotope composition similar to the mantle.
Geochimica et Cosmochimica Acta, in press available, 16p.
Africa, South Africa
deposit - Kimberly region
Abstract: Carbonate-bearing assemblages in the mantle have been interpreted to be the source for Si-undersaturated, CO2-rich magmas, including kimberlites. However, direct evidence for carbonate in the mantle is rare in the contemporary literature. Here we present petrography, trace element, and C-O-Sr-Nd-Pb isotope composition for a suite of carbonate xenoliths from the Kimberley region kimberlites to ascertain their mantle or crustal origin and gain insight to the potential for the occurrence of carbonate in the mantle. Carbonate xenoliths were found in large kimberlite blocks from the Bultfontein kimberlite and Big Hole region. The xenoliths are characterised by pale green alteration margins made of fine-grained microlites of an unknown mineral as well as spherules surrounded by glassy material. They are generally 1–4?cm in size, coarse-grained (1–2?mm), and comprised entirely of calcite. Carbonate xenoliths from the Bultfontein kimberlite have low total REE concentrations (0.2–4.9?ppm), constant 87Sr/86Sri (0.7047–0.7049) combined with variable ?Ndi (?0.1 to ?26.2) and 206Pb/204Pbi, 207Pb/204Pbi, and 208Pb/204Pbi of 16.7–18.8, 15.3–15.6, 36.5–38.4, respectively. Xenoliths from the Big Hole sample have higher 87Sr/86Sri (0.7088–0.7095), lower ?Ndi (?24.5 to ?3.8), and 206Pb/204Pbi, 207Pb/204Pbi, and 208Pb/204Pbi of 18.9–19.9, 15.7–15.8, 38.4–38.8, respectively. The ?13C values for both Bultfontein (?5.7 to ?6.6‰) and Big Hole (?4.7 to ?5.4‰) carbonates are within the typical range expected for mantle-derived carbonate. The ?18O values (15.5–17.5‰) are higher than those of mantle silicate rocks, indicative of late-stage low-temperature interaction with fluids; a common feature of groundmass calcite in the Kimberley kimberlites. The Sr- and C- isotope composition of the Bultfontein xenoliths indicates a mantle origin whereas the Big Hole xenolith Sr- and C-isotopes are more ambiguous. Isotope mixing models are inconsistent with interaction between the host kimberlite and carbonate xenoliths. Correlation between ?Ndi and ?18O values for the Bultfontein xenoliths indicates late-stage interaction with low-temperature fluids, which may also be responsible for the large range in ?Ndi. This in turn indicates that the highest ?Ndi of ?0.1 represents the primary carbonate xenolith signature, and this value overlaps typical Group I kimberlites. We discuss two possible origins for the carbonate xenoliths. (1) Carbonate xenoliths from the sub-continental lithospheric mantle (SCLM), where quenched margins and the large range of ?Ndi are related to formation in the mantle. (2) Carbonate xenoliths from an earlier phase of carbonatite magmatism. The similarity of isotope signatures of the Bultfontein carbonates to Group I kimberlite may further suggest a link between kimberlite and carbonatite volcanism such as observed elsewhere in the world.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0588-5 17p.
Africa, South Africa
deposit - De Beers dyke
Abstract: We present petrographic and mineral chemical data for a suite of samples derived from the De Beers dyke, a contemporaneous, composite intrusion bordering the De Beers pipe (Kimberley, South Africa). Petrographic features and mineral compositions indicate the following stages in the evolution of this dyke: (1) production of antecrystic material by kimberlite-related metasomatism in the mantle (i.e., high Cr-Ti phlogopite); (2) entrainment of wall-rock material during ascent through the lithospheric mantle, including antecrysts; (3) early magmatic crystallisation of olivine (internal zones and subsequently rims), Cr-rich spinel, rutile, and magnesian ilmenite, probably on ascent to the surface; and (4) crystallisation of groundmass phases (i.e., olivine rinds, Fe-Ti-rich spinels, perovskite, apatite, monticellite, calcite micro-phenocrysts, kinoshitalite-phlogopite, barite, and baddeleyite) and the mesostasis (calcite, dolomite, and serpentine) on emplacement in the upper crust. Groundmass and mesostasis crystallisation likely forms a continuous sequence with deuteric/hydrothermal modification. The petrographic features, mineralogy, and mineral compositions of different units within the De Beers dyke are indistinguishable from one another, indicating a common petrogenesis. The compositions of antecrysts (i.e., high Cr-Ti phlogopite) and magmatic phases (e.g., olivine rims, magnesian ilmenite, and spinel) overlap those from the root zone intrusions of the main Kimberley pipes (i.e., Wesselton, De Beers, Bultfontein). However, the composition of these magmatic phases is distinct from those in ‘evolved’ intrusions of the Kimberley cluster (e.g., Benfontein, Wesselton water tunnel sills). Although the effects of syn-emplacement flow processes are evident (e.g., alignment of phases parallel to contacts), there is no evidence that the De Beers dyke has undergone significant pre-emplacement crystal fractionation (e.g., olivine, spinel, ilmenite). This study demonstrates the requirement for detailed petrographic and mineral chemical studies to assess whether individual intrusions are in fact ‘evolved’; and that dykes are not necessarily produced by differentiated magmas.
Abstract: Six diamonds with a fibrous core, intermediate zone and monocrystalline outer zone (“cloudy diamonds”) from the Koffiefontein mine, South Africa, were investigated for N concentrations, carbon isotope compositions and micro-inclusion compositions along core to rim traverses. This study evaluates the nature of the change from fibrous to gem diamond growth and the relation between major element composition of high density fluid inclusions and N ? ?¹³C in fibrous growth zones. Three diamonds contain saline to carbonatitic fluid micro-inclusions with constant or increasing carbon isotope values which are inferred to have formed by varying amounts of Rayleigh fractionation in a closed system of a carbonate-bearing fluid. Continuous N ? ?¹³C fractionation trends from the fibrous to gem growth zone in two of the diamonds and equally low nitrogen aggregation states indicate formation of diamond shortly before kimberlite eruption from a single fluid without a time gap between fibrous and gem diamond growth. High major element/CO32- ratios in the growth media resulted in a constant major element composition of the fluid inclusions found in the studied fibrous diamonds. The transition from fibrous to gem diamond growth is likely caused by the precipitation of diamond reducing the degree of oversaturation of carbon in the fluid and hence decreasing the rate of diamond growth. Two other diamonds have inclusions that change from silicate minerals in the inner fibrous growth zones towards pure saline fluid compositions in the outer fibrous growth zones. This decrease in Si, Mg and Ca and increase in K and Cl in the inclusions is accompanied by a decrease in ?¹³C values and N contents. These trends are suggested to be the result from gradually mixing in more saline fluids with lower ?¹³C values. One diamond with silicic inclusions has significant N aggregation into B-centres, suggesting this fluid is different and that diamond formation occurred significantly (e.g. 1250 °C gives ?10 Ma) before the kimberlite eruption.
Abstract: The ca. 1153?Ma Premier kimberlite pipe on the Kaapvaal craton has been intruded by late-stage kimberlite and carbonatite magmas forming discrete 0.5 to 5?m wide dykes within the lower diatreme. On the basis of petrography and geochemistry, the fresh kimberlite dykes represent archetypal monticellite phlogopite kimberlite of Group-1 affinity. Their mineral compositions, however, show marked deviations from trends that are typically considered as diagnostic for Group-1 kimberlite in mineralogical-genetic classification schemes for volatile-rich ultramafic rocks. Groundmass spinel compositions are transitional between magnesian ulvöspinel (a Group-1 kimberlite hallmark feature) and titanomagnetite trends, the latter being more diagnostic for lamproite, orangeite (formerly Group-2 kimberlite), and aillikite. The Premier kimberlite dykes contain groundmass phlogopite that evolves by Al- and Ba-depletion to tetraferriphlogopite, a compositional trend that is more typical for orangeite and aillikite. Although high-pressure cognate and groundmass ilmenites from the Premier hypabyssal kimberlites are characteristically Mg-rich (up to 15?wt% MgO), they contain up to 5?wt% MnO, which is more typical for carbonate-rich magmatic systems such as aillikite and carbonatite. Manganese-rich groundmass ilmenite also occurs in the Premier carbonatite dykes, which are largely devoid of mantle-derived crystal cargo, suggesting a link to the kimberlite dykes by fractionation processes involving development of residual carbonate-rich melts and fluids. Although mineralogical-genetic classification schemes for kimberlites and related rocks may provide an elegant approach to circumvent common issues such as mantle debris entrainment, many of the key mineral compositional trends are not as robust for magma type identification as previously thought. Utilizing an experimentally constrained CO2-degassing model, it is suggested that the Premier kimberlite dykes have lost between 10 and 20?wt% CO2 during magma ascent through the cratonic lithosphere, prior to emplacement near the Earth's surface. Comparatively low fO2 values down to ?5.6 ?NNO are obtained for the kimberlite dykes when applying monticellite and perovskite oxybarometry, which probably reflects significant CO2 degassing during magma ascent rather than the original magma redox conditions and those of the deep upper mantle source. Thus, groundmass mineral oxybarometry may have little value for the prediction of the diamond preservation potential of ascending kimberlite magmas. After correction for olivine fractionation and CO2-loss, there remains a wide gap between the primitive kimberlite and carbonatite melt compositions at Premier, which suggests that these magma types cannot be linked by variably low degrees of partial melting of the same carbonated peridotite source in the deep upper mantle. Instead, fractionation processes produced carbonate-rich residual melts/fluids from ascending kimberlite magma, which led to the carbonatite dykes within Premier pipe.
Geochimica et Cosmochimica Acta, in press available 29p.
Africa, South Africa, Botswana
deposit - Koffiefontein, Letlhakane, Orapa, Finsch, De Beers Pool
Abstract: Ten individual gem-quality monocrystalline diamonds of known peridotite/eclogite paragenesis from Southern Africa (Koffiefontein, Letlhakane, Orapa) were studied for trace element concentrations and He and Ar abundances and isotopic compositions. In addition, two samples, consisting of pooled fragments of gem-quality peridotitic diamonds from Finsch and DeBeers Pool respectively, were analysed for noble gases. Previous studies (Richardson et al., 1984; Pearson et al., 1998; Gress et al., 2017; Timmerman et al., 2017) provided age constraints of 0.09, 1.0-1.1, 1.7, 2.3, and 3.2-3.4?Ga on mineral inclusions in the studied diamonds, allowing us to study trace elements and noble gases over 3 Gyr of geological time. Concentrations of trace elements in the diamonds are very low - a few hundred ppt to several tens of ppbs - and are likely dependent on the amount of sub-micron inclusions present. Trace element patterns and trace element/3He ratios of the studied monocrystalline diamonds are similar to those in fibrous diamonds, suggesting that trace elements and stable noble gas isotopes reside within the same locations in diamond and track the same processes that are reflected in the trace element patterns. We cannot discern any temporal differences in these geochemical tracers, suggesting that the processes generating them have been occurring over at least the past 2.3?Ga. 3He/4He ratios decrease and 4He and 40Ar* contents increase with increasing age of peridotitic and some eclogitic diamonds, showing the importance of in-situ radiogenic 4He and 40Ar ingrowth by the decay of U-Th-Sm and K respectively. For most gem-quality monocrystalline diamonds, uncertainties in the 3He/4He evolution of the continental lithospheric mantle combined with large analytical uncertainties and possible spatial variability in U-Th-Sm concentrations limit our ability to provide estimates of diamond formation ages using 4He ingrowth. However, the limited observed 4He ingrowth (low U?+?Th/3He) together with a R/Ra value of 5.3 for peridotitic diamond K306 is comparable to the present-day sub-continental lithospheric mantle value and supports the young diamond formation age found by Re-Os dating of sulphides in the same diamond by Pearson et al. (1998). After correction for in-situ radiogenic 4He produced since diamond formation a large variation in 3He/4He remains in ?1?Ga old eclogitic diamonds that is suggested to result from the variable influence of subducted altered oceanic crust that has low 3He/4He. Hence, the 3He/4He isotope tracer supports an origin of the diamond-forming fluids from recycled oceanic crust for eclogitic diamonds, as indicated by other geochemical proxies.
Journal of African Earth Sciences, Vol. 158, available 14p. pdf
Africa, South Africa
magmatism
Abstract: Field and sub-surface data from the Victoria West sill complex in the Karoo Large Igneous Province (ca. 180 Ma) of South Africa are used to constrain the emplacement controls of the regional-scale sill complexes in the central Karoo basin. Cross-cutting relationships point to the presence of five distinct and successively emplaced saucer-shaped sills. Growth of the sill complex was achieved through magmatic underaccretion of magma batches below earlier sills and associated uplift of the overlying strata. The magmatic underaccretion suggests that earlier sills were fully crystallized during the emplacement of later magma pulses and that the rigid (high E) dolerites, in particular, acted as stress barriers that impeded further upward propagation of steep feeder sheets. The resulting nested structure of sills-in-sills within a confined area of less than 2000 km2 also suggests the reutilization of the same or similar feeder system even after full crystallization thereof. The emplacement controls of sills in the central Karoo through stress barriers implies that sill emplacement occurred under very low deviatoric stresses or in a mildly compressional stress regime prior to the break-up of Gondwana. The swap from earlier (184-180?Ma), mainly sill complexes to later (182-174?Ma) dykes and dyke swarms is indicative of a switch in the stress field during the early stages of Gondwana break-up. We speculate that loading, thermal subsidence and lithospheric flexure associated with the emplacement of the earlier, stacked and voluminous sill complexes in the Karoo basins may have determined the formation of the large Karoo dyke swarms, particularly when coinciding with deeper crustal structures. The original and inherited basin geometry and lithospheric structure is pivotal in the development of later Karoo magmatism.
Abstract: Accurately dating the formation and modification of Earth’s sub-cratonic mantle still faces many challenges, primarily due to the long and complex history of depletion and subsequent metasomatism of this reservoir. In an attempt to improve this, we carried out the first study on peridotites from the Kaapvaal craton (Finsch Mine) that integrates results from Re-Os, Lu-Hf, Sm-Nd and Sr-isotope systems together with analyses of major-, trace- and platinum-group elements. The Finsch peridotites are well-suited for such a study because certain compositional features reflect they were highly depleted residues of shallow melting (1.5?GPa) at ambient Archean mantle temperatures. Yet, many of them have overabundant orthopyroxene, garnet and clinopyroxene compared to expected modal amounts for residues from partial melting. Finsch peridotites exhibit a wide range of rhenium depletion ages (TRD) from present day to 2.7?Ga, with a prominent mode at 2.5?Ga. This age overlaps well with a Lu-Hf isochron of 2.64?Ga (?Hf (t)?=?+26) which records silico-carbonatitic metasomatism of the refractory residues. This late Archean metasomatism is manifested by positive correlations of Pt/Ir and Pd/Ir with 187Os/188Os ratios and good correlations of modal amounts of silicates, especially garnet, with Os isotope ratios. These correlations suggest that the Highly Siderophile Elements (HSE) and incompatible element reenrichment and modal metasomatism result from one single major metasomatic event at late Archean. Our detailed study of Finsch peridotites highlights the importance of using multiple isotopic systems, to constrain the ages of events defining the evolution of lithospheric mantle. The Re-Os isotope system is very effective in documenting the presence of Archean lithosphere, but only the oldest TRD ages may accurately date or closely approach the age of the last major partial melting event. For a meaningful interpretation of the Re-Os isotope systematics the data must be combined with HSE patterns, trace-element compositions and ideally other isotopic systems, e.g. Lu-Hf. This is highlighted by the widespread evidence in Finsch peridotites of Pt, Pd and Re enrichment through significant Base Metal Sulfide (BMS) addition (mainly in the range of 0.002-0.08?wt%) that systematically shifts the mode of TRD model ages to younger ages.
Abstract: The powerpoint of the presentation made by Wiehan Smit at the SAIMM July 2019 Grade Control School has been made available by the author as a pdf file.
Abstract: The physical manifestations of plate tectonics on the modern Earth are relatively well-understood, but the nature and timing of its onset remains enigmatic, with the geodynamic regime(s) that operated during the Archaean hotly debated. This absence of a consistent geodynamic framework within which regional-scale observations can be placed limits our understanding of Archaean assemblages and associated mineral deposits. To engage with the Archaean geodynamics discussion, this thesis focuses on ultramafic-mafic complexes in the Lewisian Gneiss Complex (LGC) of the North Atlantic Craton and Johannesburg Dome of the Kaapvaal Craton. Globally, such complexes have been the subject of wide-ranging interpretations that have disparate implications for Archaean geodynamic regimes. Throughout this thesis, it is demonstrated that confidently constraining element mobility is of paramount importance when aiming to constrain the origin of Archaean ultramafic rocks, with a variety of geochemical proxies shown to be susceptible to element mobility. Notably, high field strength element anomalies - a geochemical proxy commonly used to fingerprint subduction-related magmatism - are here shown to be highly susceptible to element mobility, with the role of subduction as an Archaean geodynamic process potentially overestimated as a result. Such mobility can, however, be constrained and a primary geochemistry obtained using the integrated approach utilised here, whereby detailed petrography, bulk-rock geochemistry and mineral chemistry are examined using the context provided by rigorous field geology. Using this approach, the ultramafic-mafic complexes in the LGC are here interpreted as recording two temporally and petrogenetically distinct phases of Archaean magmatism. One group of complexes likely represents an early ultramafic-mafic crust that pre-dates the tonalite-trondhjemite-granodiorite (TTG) magmas, while a second group of complexes are interpreted as representing several layered intrusions that were emplaced into TTG. The ultramafic-mafic complexes in the Johannesburg Dome are considered to represent intrusive and extrusive remnants of an Archaean greenstone belt, contradicting a recently proposed hypothesis whereby the complexes are interpreted as fragments of an Archaean ophiolite. When combined with similar opposition to other proposed Archaean ophiolite occurrences in other cratons, this contradiction is potentially significant to the Archaean geodynamics debate, raising questions as to the validity of a > 3.6 Ga onset for modern-style plate tectonics.
Geochimica et Cosmochimica Acta, in press available 49p. Pdf
Africa, South Africa
deposit - Benfontein
Abstract: Olivine chemistry has been widely used to track the petrogenesis of mafic and ultramafic magmas from their mantle source to eruption at the surface. A major challenge in these studies is deciphering crystal growth versus diffusion controlled zoning. Here we report a multi-element approach using high-precision electron microprobe techniques to evaluate crystal growth versus diffusion in kimberlitic olivine from the Benfontein kimberlite, South Africa. These results have implications for both the petrogenesis of kimberlite magmas and the understanding of crystal growth and diffusion-based zoning in igneous olivine in general. The Benfontein olivine contain multiple phosphorous (P)-rich and P-poor zones. Core zones are characterized by homogenous low-P (<78?ppm) concentrations, consistent with xenocrystic origins. Gradational changes in Fo, Ni, Cr and other minor/trace elements at core-margins are similarly characterized by constant low-P concentrations that are indistinguishable from the central regions of the core. Olivine P-maps effectively outline the original xenocryst core, whereas gradational margins are interpreted as diffusion controlled zones related to early-stage equilibration of xenocrystic olivine with proto-/kimberlite melt. Multiple P-poor (100-150?ppm) and P-rich (200-450?ppm) concentric, oscillatory zones with inclusions of kimberlitic oxide phases are observed surrounding the low-P xenocrystic cores. Oxide phases change from chromite in the inner zones to ilmenite in the intermediate zones to magnetite-rich spinel in the outer zones of the olivine. The P-zoning corresponds with changes in Fo content implying that stages of crystal growth was preserved by both fast and slow diffusing elements rather than diffusion processes. Elements compatible with olivine (±chromite) crystallization (i.e., Ni and Cr) display a constant decrease across all zones, suggesting that magma mixing is unlikely a controlling process for P-zoning. We interpret P-rich zones to result from stages of solute trapping related of rapid disequilibrium growth driven by extrinsic factors such as changes in pressure-temperature during kimberlite evolution. In contrast, P-poor zones represent stages of equilibrium crystal growth. The outer olivine zones are characterized by an increase in Fo contents up to Fo96, and in conjunction with a change to more Fe3+-rich oxides, suggest late stage increase in fO2. Correlated Fo and P changes in the Benfontein olivine suggest that major element zonation represents an example where crystal growth-induced Fo zoning has been preserved in olivine. Furthermore, P-rich olivine zones preserve evidence for concentric growth rather than common dendritic structures seen in other occurrences. These results have implications for understanding the effect of magma dynamics and changes in pressure-temperature-fO2 conditions on olivine growth in igneous rocks.
Abstract: The late evolution of kimberlite magmas, i.e., during and-following emplacement into the upper crust, remains a-controversial aspect of kimberlite petrogenesis. Likewise, it is-unclear whether or not there is a link between melt composition-and the emplacement mechanism of intrusive kimberlites (i.e.,-planar dykes/sills vs. irregular intrusions in the root zone of-pipes). Resolving these issues is hampered by the absence of-comparative studies of late-magmatic kimberlite phases (e.g.,-apatite, monticellite, mica) in dykes, sills, and root-zone-intrusions from the same locality.-Here we report petrographic and mineral-chemical results-for groundmass phases in samples of dykes, sills, and root zone-intrusions from the Kimberley kimberlites (South Africa).-Early crystalised phases (e.g., olivine, spinel) in dykes/sills and-root-zone intrusions have indistingushable compositions, and-hence crystallised from similar primitive melts. Conversely,-apatite major element compositions are variable and can-discriminate dykes/sills (i.e., low and constant Sr, with-increasing Si) from root zone intrusions (high but variable Sr,-low and constant Si). The Sr depletion in root zone apatite is-interpreted to represent fractional crystallisation of earlier-apatite, perovskite, and calcite from a broadly similar parental-melt. Silica enrichment of apatite from dykes/sills may be-attributed to the coupled incorporation of CO32- and Si into the-apatite structure, reflecting higher CO2 contents in the melts-that formed dykes/sills. CO2 enrichment in the dykes/sills is-consistent with petrographic obervations. Dykes/sills are-enriched in carbonates, may contain dolomite, and are depleted-in mica and monticellite compared to the groundmass of rootzone-kimberlites. This suggests the melts parental to-dykes/sills have a higher CO2/H2O ratio compared to those-parental to root zone intrusions. These two distinct melt-evolution paths cannot be due to crustal contamination before-emplacement because the Sr-isotope compositions of latecrystallised-carbonates are indistinguishable in dykes/sills and-root-zone intrusions. We speculate that CO2 is better retained-in dykes/sills due to a higher confining pressure (i.e., lack of-breakthrough to the surface).-
Geochemistry, Geophysics, Geosystems, Vol. 20, 7, pp. 3311-3327.
Africa, South Africa
geophysics
Abstract: We conduct a joint inversion of teleseismic receiver functions and Rayleigh wave phase velocity dispersion from both ambient noise and earthquakes using data from 79 seismic stations in southern Africa, which is home to some of the world's oldest cratons and orogenic belts. The area has experienced two of the largest igneous activities in the world (the Okavango dyke swarm and Bushveld mafic intrusion) and thus is an ideal locale for investigating continental formation and evolution. The resulting 3?D shear wave velocities for the depth range of 0-100 km and crustal thickness measurements show a clear spatial correspondence with known geological features observed on the surface. Higher than normal mantle velocities found beneath the southern part of the Kaapvaal craton are consistent with the basalt removal model for the formation of cratonic lithosphere. In contrast, the Bushveld complex situated within the northern part of the craton is characterized by a thicker crust and higher crustal Vp/Vs but lower mantle velocities, which are indicative of crustal underplating of mafic materials and lithospheric refertilization by the world's largest layered mafic igneous intrusion. The thickened crust and relatively low elevation observed in the Limpopo belt, which is a late Archean collisional zone between the Kaapvaal and Zimbabwe cratons, can be explained by eclogitization of the basaltic lower crust. The study also finds evidence for the presence of a stalled segment of oceanic lithosphere beneath the southern margin of the Proterozoic Namaqua?Natal mobile belt.
Abstract: In the Archaean, global surface heat flow was substantially higher than today because of greater internal radiogenic heat production and primordial heat content within the Earth. Nonetheless, the lithospheric roots of Archaean cratons were apparently surprisingly cool, recording similarly low ambient temperatures to those inferred today, allowing e.g. for the stabilisation of diamond. This finding is seemingly in conflict with a generally ‘hotter’ Archaean mantle, as is widely postulated, but the paradox could be explained if the sub-cratonic lithospheric mantle was substantially thicker in the Archaean than today. Here, we report a re-investigation of the thermal structure of the Archaean Kalahari lithosphere using published and unpublished petrological data of diamond inclusions indicated to be of Archaean age. Our thermobarometric calculations agree with earlier findings that the Archaean cratonic mantle root was surprisingly cool. Importantly, the shape of the inclusion-derived P-T array deviates from the modern geotherm recorded by peridotite xenoliths. Specifically, diamond inclusions define a systematically steeper geothermal gradient than is observed in cratonic xenoliths. We find that Archaean diamond inclusion and modern xenolith P-T data cannot be reconciled by a single steady-state geotherm. The P-T conditions recorded in diamond inclusions are incompatible with the current characteristically low present-day heat-production of the overlying crust. Instead, the steeper geotherm implies high heat production in the crust during diamond formation and the distinctive geothermal gradient recorded in the studied diamond inclusions could reflect ancient mantle conditions. We modelled a suite of ‘fossil’ geotherms, with increased radiogenic heat production within the crust during the Archaean. Solutions providing very good fits with the diamond inclusion geotherm all require that the Archaean lithosphere must have extended to far greater depths than is preserved today. The required depth ranges from ~ 300 km to ~ 450 km depth, for a modern (~ 1350°C) and a significantly hotter (~ 1600°C) mantle potential temperature, respectively. In either case, it is clear that the Kalahari lithosphere must have experienced significant (at least 100 km) basal erosion subsequent to its formation.
The Journal of the Southern African Institute of Mining and Metallurgy, Vol. 119, pp. 97-103.
Africa, South Africa
deposit - Finsch
Abstract: Accurate delineation of the contact between a kimberlite pipe and country rock at production level depths is a challenge due to limited geological data. Geological information is obtained from widely spaced diamond core boreholes which are drilled either from surface or from higher mining levels within the pipe. Kimberlite pipe/country rock contacts are notoriously irregular and variable, further reducing the confidence in contact positions defined by the drill-holes. At Finsch Diamond Mine (FDM), the opportunity arose to further improve the confidence in the contact positions relative to the planned slot (end) positions of each sublevel cave tunnel during the development stage of these tunnels. As a result, the accuracy of the 3D geological model has improved.
The use of diamond drill core for this purpose is expensive due to site establishment requirements. The lengthy time taken during site establishment also delays the development of tunnels and support cycles, thereby extending the completion dates. FDM has reduced delays during development by adopting percussion drilling, in conjunction with gamma ray logging. The S36 drill rig is mounted on a moveable platform and does not require a costly and lengthy site establishment. The holes are generally drilled (0°/flat) on grade elevation, and these holes could also be drilled from the rim tunnels (developed in waste) into the kimberlite pipe. A single-boom production drill rig is normally used to drill holes about 20 m in length. On completion of the contact delineation drilling, gamma logging of the holes is conducted using the GeoVista geophysical sonde (or probe) to log the natural gamma signature of the dolomite/ kimberlite contact. The advantage of this tool is that the readings are continuous within centimetre intervals, and due to contrasting characteristics between kimberlite (rich in clay minerals) and dolomite, the contact position can be determined accurately. The better definition of contact positions also adds value to tunnel stopping distance in terms of developing the tunnel's slot at the optimum distance from the contact (easier blasting of longhole rings, avoidance of contact overbreak and premature waste ingress, and other matters relating to extraction of ore from these tunnels). This method is highly successful and has reduced development costs (on-time completion), improved definition of the pipe's contact position for geological modelling, improved blast design, and mitigated early waste ingress by maintaining the contact's integrity.
Abstract: Goldschmidtite is a new perovskite-group mineral (IMA No. 2018-034) with the ideal formula (K,REE,Sr)(Nb,Cr)O3. A single grain of goldschmidtite with a maximum dimension of ?100 ?m was found as an inclusion in a diamond from the Koffiefontein pipe in South Africa. In addition to the dark green and opaque goldschmidtite, the diamond contained a Cr-rich augite (websteritic paragenesis) and an intergrowth of chromite, Mg-silicate, and unidentified K-Sr-REE-Nb-oxide. Geothermobarometry of the augite indicates that the depth of formation was ?170 km. The chemical composition of gold-schmidtite determined by electron microprobe analysis (n = 11, WDS, wt%) is: Nb2O5 44.82, TiO2 0.44, ThO2 0.10, Al2O3 0.35, Cr2O3 7.07, La2O3 11.85, Ce2O3 6.18, Fe2O3 1.96, MgO 0.70, CaO 0.04, SrO 6.67, BaO 6.82, K2O 11.53, total 98.53. The empirical formula (expressed to two decimal places) is (K0.50La0.15Sr0.13Ba0.09Ce0.08)?0.95(Nb0.70Cr0.19Fe0.05Al0.01Mg0.04Ti0.01)?1.00O3. Goldschmidtite is cubic, space group Pm3m, with unit-cell parameters: a = 3.9876(1) Å, V = 63.404(6) Å3, Z = 1, resulting in a calculated density of 5.32(3) g/cm3. Goldschmidtite is the K-analog of isolueshite, (Na,La)NbO3. Raman spectra of goldschmidtite exhibit many second-order broad bands at 100 to 700 cm-1 as well as a pronounced peak at 815 cm-1, which is possibly a result of local ordering of Nb and Cr at the B site. The name goldschmidtite is in honor of the eminent geochemist Victor Moritz Goldschmidt (1888-1947), who formalized perovskite crystal chemistry and identified KNbO3 as a perovskite-structured compound.
Geophysical Research Letters, Vol. 46, 16, pp. 9509-9518.
Africa, South Africa
geophysics - seismics
Abstract: P and S waves travel times from large, distant earthquakes recorded on seismic stations in Botswana and South Africa have been combined with existing data from the region to construct velocity models of the upper mantle beneath southern Africa. The models show a region of higher velocities beneath the Rehoboth Province and parts of the northern Okwa Terrane and the Magondi Belt, which can be attributed to thicker cratonic lithosphere, and a region of lower velocities beneath the Damara?Ghanzi?Chobe Belt and Okavango Rift, which can be attributed a region of thinner off?craton lithosphere. This finding suggests that the spatial extent of thick cratonic lithosphere in southern Africa is greater than previously known. In addition, within the cratonic lithosphere an area of lower velocities is imaged, revealing parts of the cratonic lithosphere that may have been modified by younger magmatic events.
Journal of Southern African Studies, Vol. 45, 5, pp. 805-820.
Africa, South Africa
economics
Abstract: Existing studies on mining in Angola are mostly concerned with its social and military underpinnings and tend to analyse the diamond sector as empirically distinct from the state. In addition, little attention has been paid to how they are bound together and what these interconnections mean for the nature of politics in Angola. This gap in the literature is significant because diamond companies produce far more than revenue and profits: for some 100?years, the diamond sector has governed, policed, defended and controlled the strategic, diamond-rich provinces of Lunda Sul and Lunda Norte. In order to fill this lacuna, this article offers a case study on the role of the diamond industry for the state in Angola from the creation of the first diamond company in 1917 to the end of the Angolan civil war in 2002. Drawing on a wide range of untapped official documents and on interviews, it argues that the diamond sector has functioned historically as the conduit through which the state projects its power and secures its interests in strategic but hostile territory.
Abstract: Southern Africa is characterised by unusually elevated topography and abnormal heat flow. This can be explained by thermal perturbation of the mantle, but the origin of this is unclear. Geophysics has not detected a thermal anomaly in the upper mantle and there is no geochemical evidence of an asthenosphere mantle contribution to the Cenozoic volcanic record of the region. Here we show that natural CO2 seeps along the Ntlakwe-Bongwan fault within KwaZulu-Natal, South Africa, have C-He isotope systematics that support an origin from degassing mantle melts. Neon isotopes indicate that the melts originate from a deep mantle source that is similar to the mantle plume beneath Réunion, rather than the convecting upper mantle or sub-continental lithosphere. This confirms the existence of the Quathlamba mantle plume and importantly provides the first evidence in support of upwelling deep mantle beneath Southern Africa, helping to explain the regions elevation and abnormal heat flow.
Abstract: Eclogite mantle xenoliths from various kimberlite occurrences on the Kaapvaal craton show evidence for depth- and redox-dependent metasomatic events that led to variable base metal sulphide and incompatible element enrichments. Eclogite xenoliths from the Roberts Victor, Jagersfontein, Kimberley (Kamfersdam) and Premier kimberlites were investigated for their silicate and base metal sulphide geochemistry, stable oxygen isotope compositions and oxybarometry. The variably metasomatised eclogites had basaltic, picritic and gabbroic protolith compositions and have garnet ?18O values that range from +3.3 to +7.9‰, which, when coupled with the trace element characteristics, indicate oceanic lithosphere protoliths that had undergone variable degrees of seawater alteration. The deepest equilibrated eclogites (175220?km depth) from near the base of the Kaapvaal craton lithosphere are the most refractory and feature significant light rare earth element (LREE) depletions. They show the most oxidised redox compositions with ?logƒO2 values of FMQ-3.9 to FMQ-1.5. Subtle metasomatic overprinting of these eclogites resulted in base metal sulphide formation with relatively depleted and highly fractionated HSE compositions. These deepest eclogites and their included base metal sulphides suggest interaction with relatively oxidised melts or fluids, which, based on their HSE characteristics, could be related to precursor kimberlite metasomatism that was widespread within the Kaapvaal craton mantle lithosphere. In contrast, eclogites that reside at shallower, “mid-lithospheric” depths (140180?km) have been enriched in LREE and secondary diopside/phlogopite. Importantly, they host abundant metasomatic base metal sulphides, which have higher HSE contents than those in the deeper eclogites at the lithosphere base. The mid-lithospheric eclogites have more reducing redox compositions (?logfO2?=?FMQ-5.3 ? FMQ-3.3) than the eclogites from the lowermost Kaapvaal lithosphere. The compositional overprint of the shallower mantle eclogites resembles basaltic rather than kimberlitic/carbonatitic metasomatism, which is also supported by their relatively reducing redox state. Base metal sulphides from the mid-lithospheric eclogites have HSE abundances and distributions that are similar to Karoo flood basalts from southern Africa, suggesting a link between the identified shallow mantle metasomatism of the Kaapvaal cratonic lithosphere and the Karoo large igneous event during the Mesozoic. The sulphide-hosted platinum group element abundances of the mid-lithospheric eclogites are higher compared with their analogues from the deeper lithospheric eclogites, which in combination with their contrasting oxidation states, may imply redox-controlled HSE mobility during sulphur-rich metasomatism of continental mantle lithosphere.
Abstract: Field evidence from the Pilbara craton (Australia) and Kaapvaal craton (South Africa) indicate that modern tectonic processes may have been operating at ca. 3.2 Ga, a time also associated with a high density of preserved Archaean impact indicators. Recent work has suggested a causative association between large impacts and tectonic processes for the Hadean. However, impact flux estimates and spherule bed characteristics suggest impactor diameters of <100 km at ca. 3.5 Ga, and it is unclear whether such impacts could perturb the global tectonic system. In this work, we develop numerical simulations of global tectonism with impacting effects, and simulate the evolution of these models throughout the Archaean for given impact fluxes. We demonstrate that moderate-size (?70 km diameter) impactors are capable of initiating short-lived subduction, and that the system response is sensitive to impactor size, proximity to other impacts, and also lithospheric thickness gradients. Large lithospheric thickness gradients may have first appeared at ca. 3.5-3.2 Ga as cratonic roots, and we postulate an association between Earth’s thermal maturation, cratonic root stability, and the onset of widespread sporadic tectonism driven by the impact flux at this time.
Abstract: Topographic uplift of the southern African Plateau is commonly attributed to mantle causes, but the links between mantle processes, uplift, and erosion patterns are not necessarily straightforward. We acquired apatite (U-Th)/He (AHe) dates from eight kimberlite and basement samples from the lower reaches of the large westward-draining Orange River system with the goal of evaluating the roles of lithospheric modification and river incision on the erosion history here. Average AHe dates range from 79 to 118 Ma and thermal history models suggest that most samples are consistent with a main erosion phase at ca. 120-100 Ma, with some variability across the region indicating a complex erosion history. Major erosion overlaps with the timing of strong lithospheric thermochemical modification as recorded in xenoliths from the studied kimberlites, but the denudation pattern does not mimic the northward progression of lithospheric alteration across the study region. We attribute this area’s denudation history to a combination of mantle effects, rifting, establishment of the Orange River outlet at its current location, and later faulting. When considering these results with other kimberlite-derived surface histories from an ?1000-km-long E-W transect across the plateau, an eastward-younging trend in denudation is evident. The interplay of mantle processes and the shape of the large, west-draining Orange River basin likely control this first order-pattern.
Abstract: We addressed when plate-tectonic processes first started on Earth by examining the ca. 2.0 Ga Limpopo orogenic belt in southern Africa. We show through palinspastic reconstruction that the Limpopo orogen originated from >600 km of west-directed thrusting, and the thrust sheet was subsequently folded by north-south compression. The common 2.7-2.6 Ga felsic plutons in the Limpopo thrust sheet and the absence of an arc immediately predating the 2.0 Ga Limpopo thrusting require the Limpopo belt to be an intracontinental structure. The similar duration (?40 m.y.), slip magnitude (>600 km), slip rate (>15 mm/yr), tectonic setting (intracontinental), and widespread anatexis to those of the Himalayan orogen lead us to propose the Limpopo belt to have developed by continent-continent collision. Specifically, the combined Zimbabwe-Kaapvaal craton (ZKC, named in this study) in the west (present coordinates) was subducting eastward below an outboard craton (OC), which carried an arc equivalent to the Gangdese batholith in southern Tibet prior to the India-Asia collision. The ZKC-OC collision at ca. 2.0 Ga triggered a westward jump in the plate convergence boundary, from the initial suture zone to the Limpopo thrust within the ZKC. Subsequent thrusting accommodated >600 km of plate convergence, possibly driven by ridge push from the west side of the ZKC. As intracontinental plate convergence is a key modern plate-tectonic process, the development of the Limpopo belt implies that the operation of plate tectonics, at least at a local scale, was ongoing by ca. 2.0 Ga on Earth.
Contributions to Mineralogy and Petrology, in press available, 21p. Pdf
Africa, South Africa
deposit - Benfontein
Abstract: Primary carbonates in kimberlites are the main CO2 carriers in kimberlites and thus can be used to constrain the original carbon and oxygen-isotope composition of kimberlite melts and their deep mantle sources. However, the contribution of syn- and post-emplacement processes to the modification of the C-O-isotope composition of kimberlites is yet to be fully constrained. This study aims to shed new light on this topic through a detailed textural, compositional (major and trace elements), and in situ C-O-Sr isotopic characterisation of carbonates in the Benfontein kimberlite sills (Kimberley, South Africa). Our multi-technique approach not only reveals the petrographic and geochemical complexity of carbonates in kimberlites in unprecedented detail, but also allows identification of the processes that led to their formation, including: (1) magmatic crystallisation of Sr-rich calcite laths and groundmass; (2) crystallisation of late groundmass calcite from hydrothermal fluids; and (3) variable degrees of crustal contamination in carbonate-rich diapirs and secondary veins. These diapirs most likely resulted from a residual C-O-H fluid or carbonate melt with contributions from methane-rich fluids from the Dwyka shale wall rock, leading to higher 87Sr/86Sr and ?18O, but lower ?13C values than in pristine magmatic calcite. Before coalescing into the diapiric segregations, these fluids/melts also variably entrained early formed calcite laths and groundmass phases. Comparison between in situ and bulk-carbonate analyses confirms that O isotopic analyses of bulk carbonates from kimberlite rocks are not representative of the original isotopic signature of the kimberlite magma, whereas bulk C-isotope compositions are similar to those of the pristine magmatic carbonates. Calcite laths and most groundmass grains at Benfontein preserve isotopic values (?18O?=?6-8‰ and ?13C?=???4 to ??6‰), similar to those of unaltered carbonatites worldwide, which, therefore, probably correspond to those of their parental melts. This narrow range suggests kimberlite derivation from a mantle source with little contribution from recycled crustal material unless the recycled material had isotopic composition indistinguishable from typical mantle values.
Contributions to Mineralogy and Petrology, Vol. 175, 34 31p. Pdf
Africa, South Africa
carbonatite
Abstract: The Phalaborwa world-class phosphate deposit (South Africa) is hosted by a Paleoproterozoic alkaline complex mainly composed of phoscorite, carbonatite, pyroxenitic rocks, and subordinate fenite. In addition, syenite and trachyte occur in numerous satellite bodies. New petrological and in-situ geochemical data along with O and Sr isotope data obtained on apatite demonstrate that apatite is in the principal host rocks (pyroxenitic rocks, phoscorite and carbonatite) formed primarily by igneous processes from mantle-derived carbonatitic magmas. Early-formed magmatic apatite is particularly enriched in light rare earth elements (LREE), with a decrease in the REE content ascribed to magma differentiation and early apatite fractionation in isolated interstitial melt pockets. Rayleigh fractionation favored a slight increase in ?18O (below 1%) at a constant Sr isotopic composition. Intrusion of fresh carbonatitic magma into earlier-formed carbonatite bodies locally induced re-equilibration of early apatite with REE enrichment but at constant O and Sr isotopic compositions. In fenite, syenite and trachyte, apatite displays alteration textures and LREE depletion, reflecting interaction with fluids. A marked decrease in ?18O in apatite from syenite and trachyte indicates a contribution from ?18O-depleted meteoric fluids. This is consistent with the epizonal emplacement of the satellite bodies. The general increase of the Sr isotope ratios in apatite in these rocks reflects progressive interaction with the country rocks over time. This study made it possible to decipher, with unmatched precision, the succession of geological processes that led to one of the most important phosphate deposits worldwide.
Abstract: Mineral major and trace elements combined with Sr isotopes of clinopyroxene are used to unravel the origins and evolution of mantle eclogite and pyroxenite xenoliths from the Doornkloof-Sover orangeite dike (western Kaapvaal craton), and to investigate the generation and destruction of diamond in these rocks. Two different eclogite types are present: (1) MgO-poor eclogites (MgO?=?7.3 to 14.5?wt%; n?=?43) with accessory diamond ± corundum and kyanite; garnet grossular content (median Ca#?=?0.25) and clinopyroxene jadeite content (0.39). Reconstructed bulk rocks are LREE-depleted (median La 0.29?ppm) and have low median Cr2O3 (0.06?wt%) and incompatible trace-element contents (e.g. Sr, Zr, Ba, Pb, Th), and high Li and transition metal abundances. Some are characterised by stepped REE patterns or steep slopes in the MREE, similar to eclogites affected by interaction with dehydration fluids generated in subduction zones. These fluids may also have deposited diamond in typically reducing eclogite assemblages at diamond-stable pressures. (2) MgO-rich eclogites and pyroxenites (MgO?=?14.0 to 20.0?wt%; n?=?29), which are barren and enriched in LREE (median La 1.39?ppm), Cr2O3 (0.25?wt%) and incompatible trace elements, with lower Li and transition metal abundances than the MgO-poor group. These are typical signatures of carbonated ultramafic melt metasomatism in the mantle lithosphere. Strontium isotopic compositions vary widely in both groups, but high Cr2O3 and Ba contents are dominantly associated with 87Sr/86Sr?>?0.7055. This reflects interaction with metasomatic agents remobilised from ancient lithospheric metasomes, which eventually gave rise to regional orangeite magmatism. The presence of strong positive Eu anomalies in both groups, including two pyroxenites, requires low-pressure igneous protoliths, presumably derived from a ca. 3?Ga spreading ridge, as reported for other eclogite materials from the western Kaapvaal craton. Based on the proportions of MgO-poor and -rich eclogites and pyroxenites, approximately 40% of the diamond inventory were destroyed by mantle metasomatism centred at ~135?±?15?km depth, overlapping a low-velocity anomaly (mid-lithospheric discontinuity). Two diamondiferous orangeites ?20?km from Doornkloof-Sover contain significantly different eclogite xenolith populations: At Newlands, MgO-poor diamondiferous eclogites are present in addition to barren MgO-rich ones and pyroxenite, suggesting that the host orangeite sampled a source region equally affected by diamond-destructive mantle metasomatism, whereas at Bellsbank, all eclogites are MgO-poor and LREE-depleted. This may explain higher diamond grades reported for this locality compared to Newlands or Doornkloof-Sover.
Abstract: The application of Raman spectroscopy for the identification and characterization of minerals and related materials has increased appreciably during recent years. Raman spectroscopy has proven to be a most valuable and versatile analytical tool. Successful applications cover virtually all the mineralogical sub-disciplines, and have become more numerous in geochemistry. We present a general summary of present applications, illustrated by selected examples. In addition, we briefly point out several aspects of spectral acquisition, data reduction, and interpretation of Raman results that are important for the application of Raman spectroscopy as a reliable analytical tool.
Contributions to Mineralogy and Petrology, Vol. 175, 21p. Pdf
Africa, South Africa
deposit - Kimberley
Abstract: Kimberlites are pipe-like igneous bodies, consisting of a pyroclastic crater and diatreme, commonly underlain by coherent root-zone rocks, and with associated dyke/sill complexes. The processes that control the different modes of coherent kimberlite emplacement remain uncertain. In addition, late evolution of kimberlite melts during emplacement into the upper crust remains poorly constrained. Therefore, it is unclear whether there is a link between melt composition/evolution and the emplacement mechanism of coherent kimberlites (i.e. planar dykes/sills vs. irregular bodies in the root zone). An absence of comparative studies on late-stage magmatic phases across the different emplacement modes of coherent kimberlite from the same locality hamper resolution of these issues. Therefore, we report petrographic and mineral chemical data for groundmass apatite in samples of dyke, sill, and root-zone kimberlites from the Kimberley cluster (South Africa). Early crystallised phases (olivine, spinel, Mg-ilmenite) in dyke/sill and root-zone kimberlites have indistinguishable compositions, and hence crystallised from similar primitive melts. Conversely, apatite compositions are generally distinct in dyke/sill (low Sr, high and variable Si) and root-zone kimberlites (high and variable Sr, low Si). The Si enrichment of apatite in dykes/sills is attributed to the coupled incorporation of CO32? and SiO44? for PO43?, reflecting higher CO2 contents in their parental melts, and potentially higher Si contents due to the preferential crystallisation of carbonates over mica/monticellite. The low Sr contents of apatite in dyke/sill kimberlites reflect equilibrium with a (kimberlite) melt (i.e. DSr is close to unity for carbonate and silicate melts), whereas the higher Sr contents of apatite in root-zone kimberlites require crystallisation from, or overprinting by a H2O?±?CO2 fluid (significantly higher DSr). The relative enrichment of CO2 in kimberlite dykes/sills is evident from the abundance of carbonates, the presence of mesostasis dolomite and calcite phenocrysts in some samples, and concomitant reduced proportions of other groundmass phases (e.g. serpentine, mica, monticellite). During late alteration of kimberlite dykes/sills, monticellite is typically replaced by carbonates, whereas olivine and pleonaste are relatively stable, indicating the melts which form dykes/sills evolve to higher CO2/H2O ratios. It is unlikely that these two distinct evolutionary paths were caused by crustal contamination before or during near surface magma emplacement, because crustal assimilation is not recorded in the O and Sr isotopic composition of late crystallising olivine rinds or carbonates, respectively. We suggest that higher concentrations of CO2 are retained in kimberlite dykes/sills due to higher confining pressures (i.e. lack of breakthrough to the surface). In contrast, exsolution of CO2 from root-zone kimberlites increased melt H2O/CO2 ratios and promoted the crystallisation of mica and monticellite at the expense of dolomite and calcite. Apatite compositions have the potential to aid in the discrimination of kimberlites from lamproites (higher LREE, Sr, F, and S, lower Si contents) and carbonatites (higher LREE, F, Cl and S, lower Fe contents). However, the compositions of kimberlitic apatite overlap those from aillikites, probably due to similar late-stage melt compositions.
Journal of the Southern African Institute of Mining and Metallurgy, 8p. Pdf
Africa, South Africa
legal
Abstract: Despite the importance that barrier identification has for policy-making and industry stakeholders alike; little guidance exists on consistent processes to systematically identify barriers that are hindering the different sectors of a value chain’s expansion and growth. This article describes the development of a framework that supports the identification of barriers to growth in mineral value chains. The resultant process was applied to the case of the manganese value chain in South Africa, and revealed 31 barriers within this industry. The results were validated by a panel of experts and the feedback was used to rework and improve the framework.
Abstract: The trace element and radiogenic isotope systematics of clinopyroxene have frequently been used to characterise mantle metasomatic processes, because it is the main host of most lithophile elements in the lithospheric mantle. To further our understanding of mantle metasomatism, both solution-mode Sr-Nd-Hf-Pb and in situ trace element and Sr isotopic data have been acquired for clinopyroxene grains from a suite of peridotite (lherzolites and wehrlites), MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside), and PIC (Phlogopite-Ilmenite-Clinopyroxene) rocks from the Kimberley kimberlites (South Africa). The studied mantle samples can be divided into two groups on the basis of their clinopyroxene trace element compositions, and this subdivision is reinforced by their isotopic ratios. Type 1 clinopyroxene, which comprises PIC, wehrlite, and some sheared lherzolite samples, is characterised by low Sr (~100-200 ppm) and LREE concentrations, moderate HFSE contents (e.g., ~40-75 ppm Zr; La/Zr < 0.04), and restricted isotopic compositions (e.g., 87Sr/86Sri = 0.70369-0.70383; ?Ndi = +3.1 to +3.6) resembling those of their host kimberlite magmas. Available trace element partition coefficients can be used to show that Type 1 clinopyroxenes are close to being in equilibrium with kimberlite melt compositions, supporting a genetic link between kimberlites and these metasomatised lithologies. Thermobarometric estimates for Type 1 samples in this study indicate equilibration depths of 135-160 km within the lithosphere, thus showing that kimberlite melt metasomatism is prevalent in the deeper part of the lithosphere beneath Kimberley. In contrast, Type 2 clinopyroxenes occur in MARID rocks and coarse granular lherzolites in this study, which derive from shallower depths (<135 km), and have higher Sr (~350-1000 ppm) and LREE contents, corresponding to higher La/Zr of > ~ 0.05. The isotopic compositions of Type 2 clinopyroxenes are more variable and extend from compositions resembling the “enriched mantle” towards those of Type 1 rocks (e.g., ?Ndi = ?12.7 to ?4.4). To constrain the source of these variations, in situ Sr isotope analyses of clinopyroxene were undertaken, including zoned grains in Type 2 samples. MARID and lherzolite clinopyroxene cores display generally radiogenic but variable 87Sr/86Sri values (0.70526-0.71177), which are correlated with Sr contents and La/Zr ratios, and which might be explained by the interaction between peridotite and melts from different enriched sources within the lithospheric mantle. Most notably, the rims of these Type 2 clinopyroxenes trend towards compositions similar to those of the host kimberlite and Type 1 clinopyroxene from PIC and wehrlites. These results are interpreted to represent clinopyroxene overgrowth during late-stage (shortly before/during entrainment) metasomatism by kimberlite magmas. Our study shows that a pervasive, alkaline metasomatic event caused MARID to be generated and harzburgites to be converted to lherzolite in the lithospheric mantle beneath the Kimberley area, which was followed by kimberlite metasomatism during Cretaceous magmatism. This latter event is the time at which discrete PIC, wehrlite, and sheared lherzolite lithologies were formed, and MARID and granular lherzolites were partly modified.
Journal of Petrology, 10.1093/petrology /egaa062/5857610 90p. Pdf
Africa, South Africa
deposit - Kimberley
Abstract: Olivine is the most abundant phase in kimberlites and is stable throughout most of the crystallisation sequence, thus providing an extensive record of kimberlite petrogenesis. To better constrain the composition, evolution, and source of kimberlites we present a detailed petrographic and geochemical study of olivine from multiple dyke, sill, and root zone kimberlites in the Kimberley cluster (South Africa). Olivine grains in these kimberlites are zoned, with a central core, a rim overgrowth, and occasionally an external rind. Additional ‘internal’ and ‘transitional’ zones may occur between the core and rim, and some samples of root zone kimberlites contain a late generation of high-Mg olivine in cross-cutting veins. Olivine records widespread pre-ascent (proto-)kimberlite metasomatism in the mantle including: (a) Relatively Fe-rich (Mg# <89) olivine cores interpreted to derive from the disaggregation of kimberlite-related megacrysts (20% of cores); (b) Mg-Ca-rich olivine cores (Mg# >89; >0.05?wt.% CaO) suggested to be sourced from neoblasts in sheared peridotites (25% of cores); (c) transitional zones between cores and rims probably formed by partial re-equilibration of xenocrysts (now cores) with a previous pulse of kimberlite melt (i.e., compositionally heterogeneous xenocrysts); and (d) olivine from the Wesselton water tunnel sills, internal zones (I), and low-Mg# rims, that crystallised from a kimberlite melt that underwent olivine fractionation within the shallow lithospheric mantle. Magmatic crystallisation begins with internal olivine zones (II), which are common but not ubiquitous in the Kimberley olivine. These zones are euhedral, contain rare inclusions of chromite, and have a higher Mg# (90.0 ± 0.5), NiO, and Cr2O3 contents, but are depleted in CaO compared to the rims. Internal olivine zones (II) are interpreted to crystallise from a primitive kimberlite melt during its ascent and transport of olivine toward the surface. Their compositions suggest assimilation of peridotitic material (particularly orthopyroxene) and potentially sulfides prior to or during crystallisation. Comparison of internal zones (II) with liquidus olivine from other mantle-derived carbonate-bearing magmas (i.e., orangeites, ultramafic lamprophyres, melilitites) show that low (100×) Mn/Fe (?1.2), very low Ca/Fe (?0.6), and moderate Ni/Mg ratios (?1.1) appear to be the hallmarks of olivine in melts derived from carbonate-bearing garnet-peridotite sources. Olivine rims display features indicative of magmatic crystallisation, which are typical of olivine rims in kimberlites worldwide - i.e. primary inclusions of chromite, Mg-ilmenite and rutile, homogeneous Mg# (88.8 ± 0.3), decreasing Ni and Cr, increasing Ca and Mn. Rinds and high-Mg olivine are characterised by extreme Mg-Ca-Mn enrichment and Ni depletion, and textural relationships indicate these zones represent replacement of pre-existing olivine, with some new crystallisation of rinds. These zones likely precipitated from evolved, oxidised, and relatively low-temperature kimberlite fluids after crustal emplacement. In summary, this study demonstrates the utility of combined petrography and olivine geochemistry to trace the evolution of kimberlite magmatic systems from early metasomatism of the lithospheric mantle by (proto-)kimberlite melts, to crystallisation at different depths en route to surface, and finally late-stage deuteric/hydrothermal fluid alteration processes after crustal emplacement.
Contributions to Mineralogy and Petrology, Vol. 175, 49 dor.org./10.1007 /s00410-020-01686-0
Africa, South Africa
deposit - Kimberley
Abstract: Kimberlites are pipe-like igneous bodies, consisting of a pyroclastic crater and diatreme, commonly underlain by coherent root-zone rocks, and with associated dyke/sill complexes. The processes that control the different modes of coherent kimberlite emplacement remain uncertain. In addition, late evolution of kimberlite melts during emplacement into the upper crust remains poorly constrained. Therefore, it is unclear whether there is a link between melt composition/evolution and the emplacement mechanism of coherent kimberlites (i.e. planar dykes/sills vs. irregular bodies in the root zone). An absence of comparative studies on late-stage magmatic phases across the different emplacement modes of coherent kimberlite from the same locality hamper resolution of these issues. Therefore, we report petrographic and mineral chemical data for groundmass apatite in samples of dyke, sill, and root-zone kimberlites from the Kimberley cluster (South Africa). Early crystallised phases (olivine, spinel, Mg-ilmenite) in dyke/sill and root-zone kimberlites have indistinguishable compositions, and hence crystallised from similar primitive melts. Conversely, apatite compositions are generally distinct in dyke/sill (low Sr, high and variable Si) and root-zone kimberlites (high and variable Sr, low Si). The Si enrichment of apatite in dykes/sills is attributed to the coupled incorporation of CO32? and SiO44? for PO43?, reflecting higher CO2 contents in their parental melts, and potentially higher Si contents due to the preferential crystallisation of carbonates over mica/monticellite. The low Sr contents of apatite in dyke/sill kimberlites reflect equilibrium with a (kimberlite) melt (i.e. DSr is close to unity for carbonate and silicate melts), whereas the higher Sr contents of apatite in root-zone kimberlites require crystallisation from, or overprinting by a H2O?±?CO2 fluid (significantly higher DSr). The relative enrichment of CO2 in kimberlite dykes/sills is evident from the abundance of carbonates, the presence of mesostasis dolomite and calcite phenocrysts in some samples, and concomitant reduced proportions of other groundmass phases (e.g. serpentine, mica, monticellite). During late alteration of kimberlite dykes/sills, monticellite is typically replaced by carbonates, whereas olivine and pleonaste are relatively stable, indicating the melts which form dykes/sills evolve to higher CO2/H2O ratios. It is unlikely that these two distinct evolutionary paths were caused by crustal contamination before or during near surface magma emplacement, because crustal assimilation is not recorded in the O and Sr isotopic composition of late crystallising olivine rinds or carbonates, respectively. We suggest that higher concentrations of CO2 are retained in kimberlite dykes/sills due to higher confining pressures (i.e. lack of breakthrough to the surface). In contrast, exsolution of CO2 from root-zone kimberlites increased melt H2O/CO2 ratios and promoted the crystallisation of mica and monticellite at the expense of dolomite and calcite. Apatite compositions have the potential to aid in the discrimination of kimberlites from lamproites (higher LREE, Sr, F, and S, lower Si contents) and carbonatites (higher LREE, F, Cl and S, lower Fe contents). However, the compositions of kimberlitic apatite overlap those from aillikites, probably due to similar late-stage melt compositions.
South America, Brazil, Africa, South Africa, Guinea, Canada, Northwest Territories
deposit - Sao Luis, Juina
Abstract: Bridgmanite (Mg,Fe)SiO3, a high pressure silicate with a perovskite structure, is dominant material in the lower mantle at the depths from 660 to 2700 km and therefore is probably the most abundant mineral in the Earth. Although synthetic analogues of this mineral have been well studied, no naturally occurring samples had ever been found in a rock on the planet’s surface except in some shocked meteorites. Due to its unstable nature under ambient conditions, this phase undergoes retrograde transformation to a pyroxene-type structure. The identification of the retrograde phase as ‘bridgmanite’ in so-called superdeep diamonds was based on the association with ferropericlase (Mg,Fe)O and other high-pressure (supposedly lower-mantle) minerals predicted from theoretical models and HP-HT experiments. In this study pyroxene inclusions in diamond grains from Juina (Brazil), one single-phase (Sample SL-14) and two composite inclusions of (Mg,Fe)SiO3 coexisting with (Mg,Fe)3Al2Si3O12 (Sample SL-13), and with (Mg,Fe)3Al2Si3O12 and (Mg,Fe)2SiO4 (Sample SL-80) have been analyzed to identify retrograde phases of former bridgmanite. XRD and Raman spectroscopy have revealed that these are orthopyroxene (Opx). (Mg,Fe)2SiO4 and (Mg,Fe)3Al2Si3O12 in these inclusions are identified as olivine and jeffbenite (TAPP). These inclusions are associated with inclusions of (Mg,Fe)O (SL-14), CaSiO3 (SL-80) and composite inclusion of CaSiO3+CaTiO3 (SL-13). XRD patterns of (Mg,Fe)SiO3 inclusions indicate that they consist of polycrystals. This polycrystalline textures together with high lattice strain of host diamond around these inclusions observed from EBSD may be an evidence for the retrograde phase transition of former bridgmanite. Single-phase inclusions of (Mg,Fe)SiO3 in superdeep diamonds are suggested to represent a retrograde phase of bridgmanite and fully inherit its initial chemical composition, including a high Al and low Ni contents [Harte, Hudson, 2013; Kaminsky, 2017]. The composite inclusions of (Mg,Fe)SiO3 with jeffbenite and other silicate and oxide phases may be interpreted as exolusion products from originally homogeneous bridgmanite [Walter et al., 2011]. The bulk compositions of these composite inclusions are rich in Al, Ti, and Fe which are similar to Al-rich bridgmanite produced in experiments on the MORB composition. However, the retrograde origin of composite inclusions due to decomposition of Al-rich bridgmanite may be doubtful because each of observed phases may represent single-phase inclusions, i.e. bridgmanite and high pressure garnet (majoritic garnet), with similar compositional features.
deposit - Roberts Victor, Jagersfontein, Kimberley, Kamfersdam, Premier
Abstract: Eclogite mantle xenoliths from various kimberlite occurrences on the Kaapvaal craton show evidence for depth- and redox-dependent metasomatic events that led to variable base metal sulphide and incompatible element enrichments. Eclogite xenoliths from the Roberts Victor, Jagersfontein, Kimberley (Kamfersdam) and Premier kimberlites were investigated for their silicate and base metal sulphide geochemistry, stable oxygen isotope compositions and oxybarometry. The variably metasomatised eclogites had basaltic, picritic and gabbroic protolith compositions and have garnet ?18O values that range from +3.3 to +7.9‰, which, when coupled with the trace element characteristics, indicate oceanic lithosphere protoliths that had undergone variable degrees of seawater alteration. The deepest equilibrated eclogites (175-220 km depth) from near the base of the Kaapvaal craton lithosphere are the most refractory and feature significant light rare earth element (LREE) depletions. They show the most oxidised redox compositions with ?logƒO2 values of FMQ-3.9 to FMQ-1.5. Subtle metasomatic overprinting of these eclogites resulted in base metal sulphide formation with relatively depleted and highly fractionated HSE compositions. These deepest eclogites and their included base metal sulphides suggest interaction with relatively oxidised melts or fluids, which, based on their HSE characteristics, could be related to precursor kimberlite metasomatism that was widespread within the Kaapvaal craton mantle lithosphere. In contrast, eclogites that reside at shallower, “mid-lithospheric” depths (140-180 km) have been enriched in LREE and secondary diopside/phlogopite. Importantly, they host abundant metasomatic base metal sulphides, which have higher HSE contents than those in the deeper eclogites at the lithosphere base. The mid-lithospheric eclogites have more reducing redox compositions (?logfO2 = FMQ-5.3 ? FMQ-3.3) than the eclogites from the lowermost Kaapvaal lithosphere. The compositional overprint of the shallower mantle eclogites resembles basaltic rather than kimberlitic/carbonatitic metasomatism, which is also supported by their relatively reducing redox state. Base metal sulphides from the mid-lithospheric eclogites have HSE abundances and distributions that are similar to Karoo flood basalts from southern Africa, suggesting a link between the identified shallow mantle metasomatism of the Kaapvaal cratonic lithosphere and the Karoo large igneous event during the Mesozoic. The sulphide-hosted platinum group element abundances of the mid-lithospheric eclogites are higher compared with their analogues from the deeper lithospheric eclogites, which in combination with their contrasting oxidation states, may imply redox-controlled HSE mobility during sulphur-rich metasomatism of continental mantle lithosphere.
Abstract: The petrology and bulk-rock sulphur isotopic compositions of kimberlite samples from four localities (Bultfontein, De Beers, Kimberley, Wesselton) of the archetypal Kimberley cluster, South Africa, were used to investigate the origin(s) of S in kimberlites and gain insights into the occurrence of recycled crustal material in the source of Mesozoic kimberlites. The samples, which show variable degrees of alteration, are all hypabyssal and were derived from coherent root-zones as well as dykes and sills. Typical sulphide minerals are Cu-Fe-Ni-sulphides with less common pyrite, galena, sphalerite, and djerfisherite. They occur in a variety of textural associations, for example as groundmass phases, secondary inclusions in olivine, inclusions in matrix phases (e.g., phlogopite), or in carbonate-serpentine segregations. Barite is the most commonly observed sulphate phase. Bulk-sample ?34SVCDT values of sulphides in fresh kimberlites, which mostly do not contain barite, vary from - 2.0 to -5.7 ‰. Slightly altered kimberlite samples, in which sulphides were generally associated with serpentine, returned somewhat higher bulk-sulphide ?34SVCDT (-3.8 to +1.1 ‰). One sample from the Wesselton Water Tunnel Sills complex contains abundant barite and pyrite in its groundmass, with the latter having ?34SVCDT (+0.2 to +1.9 ‰) similar to altered kimberlites. Two further altered samples returned ?34SVCDT values (-10.1 to -13.0 ‰) that suggest a contribution from the local country rocks (Dwyka shale: ?34SVCDT from -10.2 to -10.5 ‰). All samples have near-zero ?33S values, suggesting that material displaying mass-independent fractionation has not played an important role. The negative ?34SVCDT values of fresh kimberlites from Kimberley suggest the involvement of recycled crustal material in their source, which is consistent with radiogenic isotope compositions. Overall, it appears that most kimberlitic sulphide S isotopic compositions can be explained by the action of a few typical magmatic/hydrothermal processes.
The Journal of the Southern African Insitute of Mining and Metallurgy, Vol. 119, Feb. 6p. Pdf
Africa, South Africa
DMC
Abstract: The petrology and bulk-rock sulphur isotopic compositions of kimberlite samples from four localities (Bultfontein, De Beers, Kimberley, Wesselton) of the archetypal Kimberley cluster, South Africa, were used to investigate the origin(s) of S in kimberlites and gain insights into the occurrence of recycled crustal material in the source of Mesozoic kimberlites. The samples, which show variable degrees of alteration, are all hypabyssal and were derived from coherent root-zones as well as dykes and sills. Typical sulphide minerals are Cu-Fe-Ni-sulphides with less common pyrite, galena, sphalerite, and djerfisherite. They occur in a variety of textural associations, for example as groundmass phases, secondary inclusions in olivine, inclusions in matrix phases (e.g., phlogopite), or in carbonate-serpentine segregations. Barite is the most commonly observed sulphate phase. Bulk-sample ?34SVCDT values of sulphides in fresh kimberlites, which mostly do not contain barite, vary from - 2.0 to -5.7 ‰. Slightly altered kimberlite samples, in which sulphides were generally associated with serpentine, returned somewhat higher bulk-sulphide ?34SVCDT (-3.8 to +1.1 ‰). One sample from the Wesselton Water Tunnel Sills complex contains abundant barite and pyrite in its groundmass, with the latter having ?34SVCDT (+0.2 to +1.9 ‰) similar to altered kimberlites. Two further altered samples returned ?34SVCDT values (-10.1 to -13.0 ‰) that suggest a contribution from the local country rocks (Dwyka shale: ?34SVCDT from -10.2 to -10.5 ‰). All samples have near-zero ?33S values, suggesting that material displaying mass-independent fractionation has not played an important role. The negative ?34SVCDT values of fresh kimberlites from Kimberley suggest the involvement of recycled crustal material in their source, which is consistent with radiogenic isotope compositions. Overall, it appears that most kimberlitic sulphide S isotopic compositions can be explained by the action of a few typical magmatic/hydrothermal processes. One of the most important performance indicators of a dense medium cyclone (DMC) circuit is the Tromp curve, and by extension the separation density and Ecart Probable (Ep) values. The densimetric profiles of DMC product streams have been traditionally acquired using heavy liquid sinkfloat analysis, which has certain disadvantages, such as the associated safety and health risks. More recently, non-toxic media such as lithium hetero-polytungstates (LST) have been used, with the desired densities being achieved by maintaining the solutions at specific temperatures. However, the high costs of these liquids can be prohibitive. The long turnaround time of the sink-float analysis is a further disadvantage for timeous interventions to the operating set-points of the DMC process. The RhoVol technology can generate the density distribution of a batch of particles in a rapid, accurate, repeatable, and safe manner. Additional data of interest, such as particle size and shape, are also measured and reported on a per-particle basis. Furthermore, samples can be sorted into discrete sorting bins based on any of the measured parameters of the particle, making further analyses of the material possible. This technology has applications across all commodities that use the DMC, particularly in the size fractions 25 +8 mm and 8 +3 mm. To date, laboratory results have proved very encouraging separation densities are within 5% of traditional sink-float results, and the technology is being introduced to diamond DMC plants.
Journal of Petrology, https://doi.org/ 10.1093/petrology /egaa040 50p. Pdf
Africa, South Africa
kimberlites
Abstract: Eclogite xenoliths, together with garnet pyroxenites and some mafic garnet granulites, found in kimberlites located along the southern margin of the Kaapvaal craton in southern Africa have been analysed by electron microprobe and mass spectrometry techniques to determine their geochemical characteristics. The majority of eclogites are bimineralic with garnet and omphacitic clinopyroxene in subequal proportions, with rutile as the main accessory phase; a few contain kyanite. Based on K2O in clinopyroxene and Na2O in garnet, the eclogites can be classified as Group II eclogites, and the majority are high-Ca in character. Garnet pyroxenites comprise garnet clinopyroxenites and garnet websterites. Major and trace element concentrations and isotope ratios of reconstituted bulk rock compositions of the eclogites and garnet pyroxenites allow constraints to be placed on depth of origin and likely protolith history. Calculated Fe–Mg exchange equilibration temperatures for the eclogites range from 815 to 1000?°C, at pressures of 1·7?±?0·4?GPa as determined by REE partitioning, indicating that they were sampled from depths of 50–55?km; i.e. within the lower crust of the Namaqua–Natal Belt. The garnet pyroxenites show slightly lower temperatures (686–835?°C) at similar pressures of equilibration. Initial 143Nd/144Nd and 87Sr/86Sr ratios (calculated to time of kimberlite emplacement) of both lithologies overlap the field for lower crustal samples from the Namaqua–Natal Belt. Further evidence for a crustal origin is found in the similar REE patterns shown by many of the associated garnet granulite xenoliths. Garnet pyroxenites are interpreted to have a similar origin as the associated eclogites but with the mafic protolith having insufficient Na (i.e. low modal plagioclase) to allow for development of omphacitic pyroxene. Metamorphism of the mafic protoliths to these eclogites and garnet pyroxenites is inferred to have occurred during crustal shortening and thickening associated with the collision of the Namaqua–Natal Belt with the Kaapvaal craton at 1–1·2?Ga.
The Journal of the Southern African Insitute of Mining and Metallurgy, Vol. 119, Feb, 9p. Pdf
Africa, South Africa, Zimbabwe, Namibia, Angola, DRC, Lesotho, Botswana, eSwatini
production
Abstract: Southern Africa is generally thought to be well explored, with only limited potential for major new diamond discoveries. However, Chiadzwa in Zimbabwe and reports of a significant new kimberlite find in Angola are testimony to the dangers attached to an attitude that 'there is nothing left to find'.
Since the major discoveries in the central interior of South Africa in the 1870s, diamond exploration in the region has been led by market and political factors that influence the key exploration drivers of opportunity and value proposition. Unexpected new discoveries by new players always impact on existing producers and, from time to time, denial of opportunity through political or protectionist policies has inhibited investment in exploration. Entrepreneurial exploration appetite in southern Africa will be tempered by the potential value equation and security of investment. Overlaid on this, developments in diamond recovery technologies provide opportunity to reinvigorate current mines and old prospects previously considered too difficult or costly to exploit. Position on the cost curve will remain a key factor for survival in an increasingly competitive environment.
Abstract: Because of their robust nature, diamonds survive mantle processes and protect occluded minerals since the time of diamond formation. For the Kaapvaal Craton - the archetype for craton formation and evolution - the geochemical signatures of inclusions in Koffiefontein diamonds tell a story from craton formation to evolution and from lithospheric (below about 160 km) to lower mantle (>660 km) environs. We analysed a suite of 94 lithospheric to lower mantle diamonds and their silicate and oxide inclusions. Geochemical results confirm that the diamond substrates are very depleted, with Mg#OL of 91.5-95.0 and a dominance of low-Ca (<1.8 wt% CaO), presumably dunite-derived garnet. The Si-rich nature and preserved high Mg# of the peridotitic diamond substrates beneath Koffiefontein and the formation of KNbO3 (goldschmidtite) from an extremely fractionated melt/fluid indicate that potentially both mantle- and subduction-related fluids are the cause of metasomatism in the Kaapvaal cratonic root. Mantle-like, restricted carbon isotopic compositions of both P- and E-type diamonds (avg. ?13C -5.7 ‰ and -6.6 ‰, respectively) indicate that an abundant, mantle-derived CHO fluid is responsible for diamond formation. Diamonds have a large range in nitrogen concentrations and isotopic compositions, suggesting decoupling from carbon and heterogeneous sources. ?18O of former bridgmanite and ?13C of its host diamond document a purely mantle-derived lower mantle component. Combined, these results reveal a complex and multistage evolution of the Kaapvaal Craton whereby multiple episodes of fluid and melt metasomatism re-enriched the craton already, prior to diamond formation, followed by diamond entrainment in a kimberlite possibly derived from the lower mantle.
The Journal of the Southern African Insitute of Mining and Metallurgy, Vol. 119, Feb. 10p. Pdf
Africa, South Africa
deposit - Cullinan
Abstract: In 2017, Petra Diamonds completed the construction and commissioning of a modern, fit-for-purpose diamond processing plant at Cullinan Diamond Mine (CDM). The design of CDM's milling circuit is unconventional in that it comprises an autogenous (AG) mill with a grate discharge with large ports, low-revolution jaw crushers, and high-pressure grinding roll crushers with large operating gaps. In this paper we review the design to provide guidance on what is expected from the milling circuit and to demonstrate how the design aims to address challenges experienced in the old plant, which was based on staged crushing technology. We assessed the performance of the CDM AG milling circuit from commissioning and early production stages to examine its impact along multiple dimensions. In the assessment we sought to understand the lessons from our milling circuit regarding diamond liberation, energy consumption, and the future of diamond processing as a whole.
Abstract: The thermobarometric analysis of inclusions in lithospheric diamonds indicates that they originated from a wide range of depths, with a global mode at ca. 170±15 km [1]. Studies based on diamond depth distribution at global scale, however, cannot clarify if this mode reflects a real concentration of diamonds, preferential sampling of materials from this level by rising kimberlites, or even a statistical distribution within the hard limits imposed by diamond stability, lithosphere thickness, and mantle adiabat under typical cratonic thermal regimes. We addressed this problem by comparing depth distributions for peridotitic diamonds from the three localities that have been the most prolific for diamond geobarometry (Cullinan, Kimberley and Voorspoed, South Africa) with those of mantle xenocrysts from the same kimberlite sources. P-T estimates indicate that the diamonds were formed at T higher, equal or lower than the ambient geotherm. They may record old mantle thermal regimes or local thermal perturbations related to infiltration of parent fluids or melts. Nonetheless, the diamonds show similar depth distributions for different localities, with a distinct mode at ?175 ?? 10 km. The similarity of these distributions with that calculated for peridotitic diamonds worldwide, as well as the lack of systematic correlation with kimberlite sampling efficiency as recorded by mantle xenocrysts, suggests that this mode has genetic significance. Based on observed depth distributions at both local and global scale and on thermodynamic modeling of COH fluids, diamond-forming processes are predicted to become less efficient with decreasing depth from at least ?160 km. In addition, diamond endowment near the base of the lithosphere may be negatively affected by infiltration of carbon-undersaturated melts. Considering the poor correlation between diamond and xenocryst depth distributions in single kimberlites or kimberlite clusters, even limited xenocryst records from diamond favorable depths (especially the 160-190 km interval) may correspond to significant diamond potential.
South America, Brazil, Africa, South Africa, Canada, Northwest Territories
geochronology
Abstract: Kimberlites emplaced since ~2 Ga show Nd and Hf isotopic compositions that follow a remarkably consistent linear evolution [1]. However, kimberlites emplaced <200 Ma within a few thousand kilometers of the western paleo-margin of Pangea (i.e. Brazil, southern Africa, and Lac de Gras in western Canada) deviate towards more enriched Nd and Hf isotopic compositions possibly due to contribution by recycled crustal material, introduced to the deep kimberlite source via subduction [1]. To address this anomaly further we have compared new and existing geochronological and Nd isotopic data for 28 kimberlites from Lac de Gras (LDG; ca. 47 - 75 Ma) with their olivine and spinel mineral chemistries. Olivine grains typically include mantle-derived xenocrystic cores (Mg# = 83.5-94.2) overgrown by magmatic rims with relatively constant Mg# values. Olivine rims and chromite are the first magmatic phases to crystallise from kimberlite and can be used as proxies for primitive melt compositions. The average Mg# of olivine cores from each kimberlite is positively correlated with average olivine rim Mg#, suggesting that assimilation of heterogeneous lithospheric mantle contributed to the primitive melt compositions. The ?Nd(i) values from whole-rock and perovskite from LDG kimberlites vary between -3.4 and -0.4 that are negatively correlated with their emplacement ages. This correlation is indicative of an evolving kimberlite source which may have resulted from a progressively lower contribution of recycled material. No systematic relationships were observed between olivine rim or chromite compositions and age or Nd isotopic composition. This observation highlights decoupling between kimberlite source evolution and primitive melt compositions due to the combined effects of crustal recycling in the kimberlite source and lithospheric mantle assimilation during kimberlite ascent.
Africa, South Africa, Guinea, Australia,South America, Brazil, Canada, Northwest Territories
deposit - Koffiefontein, Kankan, Lac de Gras, Juina, Machado, Orroroo
Abstract: (Mg,Fe)SiO3 bridgmanite is the dominant phase in the lower mantle; however no naturally occurring samples had ever been found in terrestrial samples as it undergoes retrograde transformation to a pyroxene-type structure. To identify retrograde phases of former bridgmanite single-phase and composite inclusions of (Mg,Fe)SiO3 in a series of superdeep diamonds have been examined with electron microscopy, electron microprobe, Raman spectroscopy and X-ray diffraction techniques. Our study revealed that (Mg,Fe)SiO3 inclusions are represented by orthopyroxene. Orthopyroxenes in single-phase and composite inclusions inherit initial chemical composition of bridgmanites, including a high Al and low Ni contents. In composite inclusions they coexist with jeffbenite (ex-TAPP) and olivine. The bulk compositions of these composite inclusions are rich in Al, Ti, and Fe, which are similar but not fully resembling Al-rich bridgmanite produced in experiments on the MORB composition. The retrograde origin of composite inclusions due to decomposition of Al-rich bridgmanite may be doubtful because each of observed minerals may represent coexisting HP phases, i.e. bridgmanite or ringwoodite.
Abstract: Mineral carbonation is a form of carbon capture, utilization and storage (CCUS) that aims to transform excess CO2 into environmentally benign carbonate minerals which are geologically stable. Here, we investigated the reactivity of processed kimberlite and kimberlite ore from the Venetia Diamond Mine (South Africa). Highly reactive phases, such as brucite [Mg(OH)2], are uncommon in the samples collected from Venetia necessitating the development of new strategies for mineral carbonation. Kimberlite ore and tailings from this mine consist of a clay-rich mineral assemblage that is dominated by lizardite (a serpentine mineral) and smectites. Smectites are swelling clays that can act as a source of Mg and Ca for carbonation reactions via cation exchange, dissolution and/or direct replacement of smectites to form carbonate phases. Although carbonation of serpentine and brucite has long been a focus of CCUS in mine wastes [1], smectite carbonation has not been explored in this setting. Quantitative X-ray diffraction using Rietveld refinements coupled with Fourier-transform infrared spectroscopy indicate that smectites of stevensite-saponite composition are abundant in the Venetia samples (1.3-15.4 wt.%). Synchrotron-based X-ray fluorescence mapping correlated with scanning and transmission electron microscopy show that smectites are distributed as altered, smooth regions measuring from 1 to 20 ?m in breadth. These phases are rich in Mg and Ca and Al-poor. To better understand the behaviour/reactivity of smectites during the cation exchange process, we have used batch experiments with pure endmembers of Ca-, Mg- and Na-montmorillonite under different treatment conditions (NH4-citrate, NH4-O-acetate, NH4-Cl and Na3-citrate). After 24 hours of reaction, ICP-MS analyses reveal that the four treatments have the same efficiency for Ca and Mg exchange, while NH4-Cl and NH4- O-acetate treatments minimize calcite dissolution. Our end goals are to optimize settling time and to maximize extraction of Ca and Mg for carbonation reactions during ore processing.
Marine and Petroleum Geology, Vol. 28, pp. 1385-1401.
Africa, South Africa
geomorphology
Abstract: The application of the onset of supercontinentality, the “Great Oxidation Event” (GOE) and the first global scale glaciation in the Neoarchaean-Palaeoproterozoic as panacea-like events providing a framework or even chronological piercing points in Earth’s history at this time, is questioned. There is no solid evidence that the Kaapvaal craton was part of a larger amalgamation at this time, and its glacigenic record is dominated by deposits supporting the operation of an active hydrological cycle in parallel with glaciation, thereby arguing against the “Snowball Earth Hypothesis”. While the Palaeoproterozoic geological record of Kaapvaal does broadly support the GOE, this postulate itself is being questioned on the basis of isotopic data used as oxygen-proxies, and sedimentological data from extant river systems on the craton argue for a prolongation of the greenhouse palaeo-atmosphere (possibly in parallel with a relative elevation of oxygen levels) which presumably preceded the GOE. The possibility that these widespread events may have been diachronous at the global scale is debated.
Abstract: Eclogite xenoliths, together with garnet pyroxenites and some mafic garnet granulites, found in kimberlites located along the southern margin of the Kaapvaal craton in southern Africa have been analysed by electron microprobe and mass spectrometry techniques to determine their geochemical characteristics. The majority of eclogites are bimineralic with garnet and omphacitic clinopyroxene in subequal proportions, with rutile as the main accessory phase; a few contain kyanite. Based on K2O in clinopyroxene and Na2O in garnet, the eclogites can be classified as Group II eclogites, and the majority are high-Ca in character. Garnet pyroxenites comprise garnet clinopyroxenites and garnet websterites. Major and trace element concentrations and isotope ratios of reconstituted bulk rock compositions of the eclogites and garnet pyroxenites allow constraints to be placed on depth of origin and likely protolith history. Calculated Fe-Mg exchange equilibration temperatures for the eclogites range from 815 to 1000?°C, at pressures of 1•7?±?0•4?GPa as determined by REE partitioning, indicating that they were sampled from depths of 50-55?km; i.e. within the lower crust of the Namaqua-Natal Belt. The garnet pyroxenites show slightly lower temperatures (686-835?°C) at similar pressures of equilibration. Initial 143Nd/144Nd and 87Sr/86Sr ratios (calculated to time of kimberlite emplacement) of both lithologies overlap the field for lower crustal samples from the Namaqua-Natal Belt. Further evidence for a crustal origin is found in the similar REE patterns shown by many of the associated garnet granulite xenoliths. Garnet pyroxenites are interpreted to have a similar origin as the associated eclogites but with the mafic protolith having insufficient Na (i.e. low modal plagioclase) to allow for development of omphacitic pyroxene. Metamorphism of the mafic protoliths to these eclogites and garnet pyroxenites is inferred to have occurred during crustal shortening and thickening associated with the collision of the Namaqua-Natal Belt with the Kaapvaal craton at 1-1•2?Ga.
Nature Communications, doi:.org/10.1038/ s41467-020-17442 -8 11p. Pdf
Africa, South Africa, Russia, Siberia
water
Abstract: Trace amounts of water dissolved in minerals affect density, viscosity and melting behaviour of the Earth’s mantle and play an important role in global tectonics, magmatism and volatile cycle. Water concentrations and the ratios of hydrogen isotopes in the mantle give insight into these processes, as well as into the origin of terrestrial water. Here we show the presence of molecular H2 in minerals (omphacites) from eclogites from the Kaapvaal and Siberian cratons. These omphacites contain both high amounts of H2 (70 to 460 wt. ppm) and OH. Furthermore, their ?D values increase with dehydration, suggesting a positive H isotope fractionation factor between minerals and H2-bearing fluid, contrary to what is expected in case of isotopic exchange between minerals and H2O-fluids. The possibility of incorporation of large quantities of H as H2 in nominally anhydrous minerals implies that the storage capacity of H in the mantle may have been underestimated, and sheds new light on H isotope variations in mantle magmas and minerals.
Abstract: The thermobarometric analysis of inclusions in lithospheric diamonds has shown that these diamonds may originate from a wide range of depths, with a global mode at ~175 ± 15 km. Studies based on diamond depth distribution at global scale, however, cannot clarify if this mode reflects a real concentration of diamonds, preferential sampling of materials from this level by ascending kimberlites, or simply a statistical distribution within the hard limits imposed by diamond stability, lithosphere thickness and mantle adiabat under typical cratonic thermal regimes. We addressed this problem by comparing depth distributions for peridotitic diamonds from the three localities that have been the most prolific for diamond geobarometry (Cullinan, Kimberley and Voorspoed, South Africa) with those of mantle xenocrysts from the same kimberlite sources. The revised P-T estimates indicate that the diamonds were formed at T higher, equal or lower than the ambient geotherm recorded by the xenocrysts. These conditions may represent old mantle thermal regimes or local thermal perturbations related to infiltration of parental fluids or melts. Nonetheless, the studied diamonds show similar depth distributions for the different localities, with a distinct mode at ?180 ± 10 km. The similarity of these distributions with that calculated for peridotitic diamonds worldwide, as well as the lack of systematic correlation with kimberlite sampling efficiency as recorded by mantle xenocrysts, suggests that this mode has genetic significance. Based on observed depth distributions and thermodynamic modeling of COH fluids, diamond-forming processes are predicted to become less efficient with decreasing depth from at least ?165 km. In addition, diamond endowment near the base of the lithosphere may be negatively affected by infiltration of carbon-undersaturated melts or fluids after diamond formation. Considering the poor correlation between diamond and xenocryst depth distributions in single kimberlites or kimberlite clusters, even limited xenocryst records from diamond favorable depths (especially from the 160-190 km interval) may correspond to significant diamond potential.
Journal of Petrology, in press available, 90p. Pdf
Africa, South Africa
deposit - Kimberley
Abstract: Olivine is the most abundant phase in kimberlites and is stable throughout most of the crystallization sequence, thus providing an extensive record of kimberlite petrogenesis. To better constrain the composition, evolution, and source of kimberlites we present a detailed petrographic and geochemical study of olivine from multiple dyke, sill, and root zone kimberlites in the Kimberley cluster (South Africa). Olivine grains in these kimberlites are zoned, with a central core, a rim overgrowth, and occasionally an external rind. Additional ‘internal’ and ‘transitional’ zones may occur between the core and rim, and some samples of root zone kimberlites contain a late generation of high-Mg olivine in cross-cutting veins. Olivine records widespread pre-ascent (proto-)kimberlite metasomatism in the mantle including the following features: (1) relatively Fe-rich (Mg# <89) olivine cores interpreted to derive from the disaggregation of kimberlite-related megacrysts (20?% of cores); (2) Mg-Ca-rich olivine cores (Mg# >89; >0•05?wt% CaO) suggested to be sourced from neoblasts in sheared peridotites (25?% of cores); (3) transitional zones between cores and rims probably formed by partial re-equilibration of xenocrysts (now cores) with a previous pulse of kimberlite melt (i.e. compositionally heterogeneous xenocrysts); (4) olivine from the Wesselton water tunnel sills, internal zones (I), and low-Mg# rims, which crystallized from a kimberlite melt that underwent olivine fractionation and stalled within the shallow lithospheric mantle. Magmatic crystallization begins with internal olivine zones (II), which are common but not ubiquitous in the Kimberley olivine. These zones are euhedral, contain rare inclusions of chromite, and have a higher Mg# (90•0 ± 0•5), NiO, and Cr2O3 contents, but are depleted in CaO compared with the rims. Internal olivine zones (II) are interpreted to crystallize from a primitive kimberlite melt during its ascent and transport of olivine toward the surface. Their compositions suggest assimilation of peridotitic material (particularly orthopyroxene) and potentially sulfides prior to or during crystallization. Comparison of internal zones (II) with liquidus olivine from other mantle-derived carbonate-bearing magmas (i.e. orangeites, ultramafic lamprophyres, melilitites) shows that low (100×) Mn/Fe (?1•2), very low Ca/Fe (?0•6), and moderate Ni/Mg ratios (?1•1) appear to be the hallmarks of olivine in melts derived from carbonate-bearing garnet-peridotite sources. Olivine rims display features indicative of magmatic crystallization, which are typical of olivine rims in kimberlites worldwide; that is, primary inclusions of chromite, Mg-ilmenite and rutile, homogeneous Mg# (88•8 ± 0•3), decreasing Ni and Cr, and increasing Ca and Mn. Rinds and high-Mg olivine are characterized by extreme Mg-Ca-Mn enrichment and Ni depletion, and textural relationships indicate that these zones represent replacement of pre-existing olivine, with some new crystallization of rinds. These zones probably precipitated from evolved, oxidized, and relatively low-temperature kimberlite fluids after crustal emplacement. In summary, this study demonstrates the utility of combined petrography and olivine geochemistry to trace the evolution of kimberlite magmatic systems from early metasomatism of the lithospheric mantle by (proto-)kimberlite melts, to crystallization at different depths en route to surface, and finally late-stage deuteric or hydrothermal fluid alteration after crustal emplacement.
Abstract: During the past two decades significant progress has been made in understanding the origin and evolution of kimberlites, including relationships to other diamondiferous magma types such as lamproites and aillikites. However, the association of kimberlites and carbonatites on continental shields remains poorly understood, and two opposing ideas dominate the debate. While one school of thought argues that primary carbonatite melts transform into hybrid carbonated silicate magmas akin to kimberlites by assimilation of cratonic mantle material, others use geochemical evidence to show that carbonatite magmas can evolve from near-primary kimberlite melts within the cratonic lithosphere. The 1.15 Ga Premier kimberlite pipe on the Kaapvaal craton in South Africa hosts several kimberlite and carbonatite dykes. Reconstructions of magma compositions suggest that up to 20 wt.% CO2 was lost from near-primary kimberlite melts during ascent through the cratonic lithosphere, but the carbonatite dyke compositions cannot be linked to the kimberlite melts via differentiation. Geochemical evidence, including mantle-like ?13C compositions, suggests that the co-occurring kimberlite and carbonatite dykes represent two discrete CO2-rich magma batches derived from a mixed source in the convecting upper mantle. The carbonatites probed a slightly more depleted source component in terms of Sr-Nd-Hf isotopic compositions relative to the peridotitic matrix that was more effectively tapped by the kimberlites (87Sr/86Sri = 0.70257 to 0.70316 for carbonatites vs. 0.70285 to 0.70546 for kimberlites; ?Ndi = +3.0 to +3.9 vs. +2.2 to +2.8; ?Hfi = -2.2 to +0.7 vs. -5.1 to -1.9). Platinum-group element systematics suggest that assimilation of refractory lithospheric mantle material by the carbonatite melts was negligible (<1 vol.%), whereas between 5 - 35 vol.% of digested cratonic peridotite account for the kimberlite compositions, including the low 187Os/188Os signature (?Osi = -12.7 to -4.5). The kimberlite and carbonatite dykes show similarly strong Nd-Hf isotope decoupling (??Hfi = -10.7 to -7.6 vs. -8.8 to -6.1), regardless of the variable lithospheric mantle imprints. This observation suggests a common sublithospheric origin of the negative ??Hf signature, possibly linked to ancient recycled oceanic crust components in the convecting upper mantle to transition zone sources of CO2-rich magmatism. Mesoproterozoic kimberlite and carbonatite magmatism at Premier was coeval with subduction and collision events along the southern Kaapvaal craton margin during the 1,220 -1,090 Ma Namaqua-Natal orogeny associated with Rodinia supercontinent formation. Thermochronology suggests that the entire Kaapvaal craton was affected by this collisional tectonic event, and it appears that the changing lithospheric stress-field created pathways for deep-sourced kimberlite and carbonatite magmas to reach Earth’s surface. We find that collision-induced (e.g., Premier) and continental breakup-related (e.g., Kimberley) kimberlite magmas are compositionally indistinguishable, with the inference that plate tectonic processes aid solely in the creation of magma ascent pathways without a major influence on deep mantle melting beneath cratons. It follows that on-craton kimberlite magmatism in the hinterland of collision zones is not necessarily more likely to entrain large sublithospheric diamonds than kimberlite eruptions linked to continental breakup. This implies that Premier’s world-class endowment with ‘ultradeep’ Type-II diamonds is not causally related to its setting behind an active orogenic front.
Abstract: Newlands and Bobbejaan kimberlites, South Africa, contain suites of highly chromian, garnet-rich peridotites amongst their xenolith population and an investigation of these xenoliths has been targeted because there is an overlap of mineral compositions withthe garnet-chromite-olivine paragenesis found as inclusions in diamonds. A high proportion of garnets and chromites in these rocks plot in the diamond facies fields on Cr2O3-CaO and Cr2O3-MgO wt. % plots respectively. However, it has also been found that many Cr-rich assemblages are clinopyroxene-bearing (lherzolitic) as well as harzburgitic (i.e. forming arange of chromite-garnet peridotite assemblages). Many samples have garnets with inclusions of serpentine ± chromite (+ clinopyroxene in lherzolitic samples) whose arrangement are sometimes indicative of exsolution or annealed exsolution textures. Initial bulk REE patterns were calculated for the pre-exsolution, pre-metasomatism, high-Cr garnets. The patterns found are humped for harzburgitic samples and relatively flat for lherzolitic ones. These appear to be closely linked to the concentration of Ca in garnet indicative of a single-stage formation process for the humped profiles. The profiles were later modified by exsolution of pyroxenes (with a clear link between Ca content of garnet and the garnet/clinopyroxene partition coefficients) and, in a few cases, by metasomatism causing a zonation of REE.Most of the garnets have strongly developed zonation patterns which are a result of diffusion towards the matrix (external zonation) followed by zonation towards inclusions (internal zonation). Cr-Al and Mg-Ca inter-diffuse in both types of zonation; Ti may also be strongly zoned, whereas Fe is not distinctly zoned in any sample. External zonation may be divided into ‘P-T re-equilibration’ and ‘metasomatic’ types, where the former type conforms to down-P-T garnet-spinel transition reaction simulations and the latter does not. All internal zonations conform to down P-T reaction simulations. All the zonation profiles conform well to diffusion controlled reaction models. External P-T re-equilibration is modelled to have occurred on an order of magnitude greater timescale than internal zonation (~5 Ma compared to ~0.5 Ma using DMg= 10-20m2 /s). Metasomatic zonation occurs over the longest diffusion distances and is modelled to have timescales up to 20 Ma. Based upon the geometries of chemical heterogeneity in the minerals analysed, a sequence of events has been proposed for the evolution of the Newlands and Bobbejaan samples: (1) Earliest known mineralogy. Thereis little evidence for the events prior to and during this stage. However, the modal mineralogy is postulated to have been more garnet and olivine-rich than seen in the samples and the crystals more chemically homogeneous. The P and T in samples are modelled to have the highest Ps and Ts of all stages (potentially > 65kb and > 1350°C). (2) Exsolution.This stage represents the initiation of an event which significantly lowered P and T where spinel and pyroxene exsolved from garnet. (3a) External zonation - P-T re-equilibration and metasomatism. These events are contiguous with stage 2 and P-T estimates for this stage indicate further lowering of P and T. This is accompanied by modification of a few samples by the infiltration of metasomatic fluid. (3b) Internal zonation – P-T re-equilibration. This stage represents the final lowering of P and T, yielding final P-T estimates on clinopyroxene inclusion-garnet boundaries of 38-50 kb and 900-1150°C. These P-T estimates place samples plot on a relatively cool continental steady state geotherm. (4) Kimberlite eruption. The initial formation of the garnet-rich rock types with their (calculated) highly chromian composition and particular initial REE compositions appears to be related to a major depletion event with subsequent burial. Differential interaction with a CO2-bearing fluid would generate the range of harzburgitic and lherzolitic compositions found. However it is acknowledged that this is difficult to determine and constrain because of the lack of preservation of evidence prior to Stage 2.The down-P-T event has a similar timescale and associated uplift rate to be related to continent-continent collision according to the time scales for diffusion. The contemporaneous metasomatism leads to postulation that the event may have been related to the continental accretion of the eastern and western parts of the Kaapvaal craton in the late Archaean. In terms of the relation to diamond, it was found that samples with high-Cr harzburgitic garnets tended to yield P-T estimates that were most substantially into the diamond stability field based upon the Cr-Al partitioning between garnet and spinel and also modelling the samples using the computer programme known as‘Perplex’. Clinopyroxene-bearing samples (i.e. those with a bulk rock composition higher inCa) tended to indicate higher temperatures of equilibration. Cr-spinels from the harzburgitic paragenesis have higher Mg and lower Ti than the lherzolitic Cr-spinels, but overlapping Cr compositions at high Cr and may be differentiated on Cr-Mg and Cr-Ti compositional plots.
Abstract: The structural depression that occupies the Okavango Basin in southern Africa comprises a depo?centre within the intracratonic Kalahari Basin where sediments of the Cenozoic Kalahari Group have accumulated. The Okavango Basin has been formed due to stretching and subsidence at an area of diffused deformation, southwestwards to the main East African Rift System (EARS). Sediments from two full Kalahari Group sequences, located on opposite sides of the Gumare Fault that forms a major fault within the Okavango Basin, were studied to determine their provenance and chronology. Terrestrial Cosmogenic Nuclide (TCN) 26Al/10Be burial dating was used to constrain a chronostratigraphical framework, and Pb, Sr, and Nd isotopic ratios combined with geochemical and sedimentological analyses were applied to track the source areas of the sediments.Results indicate the following sequence of basin filling: (a) Accumulation between ca. 4-3 Ma during which the currently downthrown (southern) block received a mixture of sediments mostly from the Choma?Kalomo, Ghanzi?Chobe, and Damara terranes, and possibly from the Lufilian Belt and/or Karoo basalts during earlier stages of deposition. Simultaneously, the upthrown (northern) block received sediments from more distant Archean sources in the Zimbabwe and/or Kasai cratons, (b) Hiatus in sedimentation occurred at both sites between ca. 3-2 Ma, (c) Sediments on both sides of the Gumare Fault share a similar source (Angolan Shield) with minor distinct contributions to the downthrown block from the Kasai Craton and local sources input to the upthrown block, and (d) Regional distribution of aeolian sand since at least 1 Ma. The change in source areas is attributed to rearrangements of the drainage systems that were probably linked to vertical crustal movements on the margins of the Okavango Basin. The tectonically induced morphodynamics controlled the landscape evolution of the endorheic basin where vast lakes, wetlands and salt pans have developed through time.
White-Gaynor, A.L., Nyblade, A.A., Durrheim, R., Raveloson, R., van der Meijde, M., Fadel, I., Paulssen, H., Kwadiba, M., Ntibinyane, O., Titus, N., Sitali, M.
Geochemistry, Geophysics, Geosystems, 10.1029/GC008925 20p. Pdf
Africa, South Africa
Geophysics, seismic
Abstract: We report new P and S wave velocity models of the upper mantle beneath southern Africa using data recorded on seismic stations spanning the entire subcontinent. Beneath most of the Damara Belt, including the Okavango Rift, our models show lower than average velocities (?0.8% Vp; ?1.2% Vs) with an abrupt increase in velocities along the terrane's southern margin. We attribute the lower than average velocities to thinner lithosphere (~130 km thick) compared to thicker lithosphere (~200 km thick) immediately to the south under the Kalahari Craton. Beneath the Etendeka Flood Basalt Province, higher than average velocities (0.25% Vp; 0.75% Vs) indicate thicker and/or compositionally distinct lithosphere compared to other parts of the Damara Belt. In the Rehoboth Province, higher than average velocities (0.3% Vp; 0.5% Vs) suggest the presence of a microcraton, as do higher than average velocities (1.0% Vp; 1.5% Vs) under the Southern Irumide Belt. Lower than average velocities (?0.4% Vp; ?0.7% Vs) beneath the Bushveld Complex and parts of the Mgondi and Okwa terranes are consistent with previous studies, which attributed them to compositionally modified lithosphere resulting from Precambrian magmatic events. There is little evidence for thermally modified upper mantle beneath any of these terranes which could provide a source of uplift for the Southern African Plateau. In contrast, beneath parts of the Irumide Belt in southern and central Zambia and the Mozambique Belt in central Mozambique, deep?seated low velocity anomalies (?0.7% Vp; ?0.8% Vs) can be attributed to upper mantle extensions of the African superplume structure.
Canada, Nunavut, Southampton Island, Africa, Kaapvaal
craton
Abstract: Ancient rocks have survived plate tectonic recycling for billions of years, but key questions remain about how and when they were exhumed to the surface. Constraining exhumation histories over long timescales is a challenge because much of the rock record has been lost to erosion. Argon and helium noble gas thermochronology can reconstruct deep-time <350 °C thermal histories by using the distinct temperature sensitivities of minerals such as feldspar, zircon, and apatite, while exploiting grain size and radiation damage effects on diffusion kinetics. Resolution of unique time-temperature paths over long timescales requires multiple chronometers, appropriate kinetic models, and inverse simulation techniques to fully explore and constrain possible solutions. Results suggest that surface histories of ancient continental interiors are far from uninteresting and may merely be misunderstood.
Lithos, doi.org/10.1016/ j.lithos.2020.105918 67p. Pdf
Africa, South Africa
deposit - Roberts Victor
Abstract: Platinum-group elements (PGE) display a chalcophile behaviour and are largely hosted by base metal sulphide (BMS) minerals in the mantle. During partial melting of the mantle, BMS release their metal budget into the magma generated. The fertility of magma sources is a key component of the mineralisation potential of large igneous provinces (LIP) and the origin of orthomagmatic sulphide deposits hosted in cratonic mafic magmatic systems. Fertility of mantle-derived magma is therefore predicated on our understanding of the abundance of metals, such as the PGE, in the asthenospheric and lithospheric mantle. Estimations of the abundance of chalcophile elements in the upper mantle are based on observations from mantle xenoliths and BMS inclusions in diamonds. Whilst previous assessments exist for the BMS composition and chalcophile element budget of peridotitic mantle, relatively few analyses have been published for eclogitic mantle. Here, we present sulphide petrography and an extensive in situ dataset of BMS trace element compositions from Roberts Victor eclogite xenoliths (Kaapvaal Craton, South Africa). The BMS are dominated by pyrite-chalcopyrite-pentlandite (± pyrrhotite) assemblages with S/Se ratios ranging 1200 to 36,840 (with 87% of analyses having S/Se this editing is incorrect. This should read "(with 87% of analyses having S/Se < 10,000)" Please note the 100 ppm) and are characteristically enriched in Os, Ir, Ru and Rh. Nano- and micron-scale Pd-Pt antimonide, telluride and arsenide platinum-group minerals (PGM) are observed spatially associated with BMS. We suggest that the predominance of pyrite in the xenoliths reflects the process of eclogitisation and that the trace element composition of the eclogite BMS was inherited from oceanic crustal protoliths of the eclogites, introduced into the SCLM via ancient subduction during formation of the Colesberg Magnetic Lineament c. 2.9 Ga and the cratonisation of the Kaapvaal Craton. Crucially, we demonstrate that the PGE budget of eclogitic SCLM may be substantially higher than previously reported, akin to peridotitic compositions, with significant implications for the PGE fertility of cratonic mafic magmatism and metallogenesis. We quantitatively assess these implications by modelling the chalcophile geochemistry of an eclogitic melt component in parental magmas of the mafic Rustenburg Layered Suite of the Bushveld Complex.
South African Journal of Geology, Vol. 123, 4, pp. 597-614. pdf
Africa, South Africa
alkaline rocks
Abstract: Numerous Mesoproterozoic alkaline intrusions belonging to the Pilanesberg Alkaline Province are present within the Transvaal sub-basin of the Kaapvaal Craton. The Pilanesberg Complex is the best-known example; it represents one of the world’s largest alkaline complexes, and is associated with a northwest-southeast trending dyke swarm that extends from Botswana to the southwest of Johannesburg. This paper documents the results of a petrological and geochemical study of a thin mafic sill (here referred to as an alkaline igneous body, AIB), which intrudes the ca. 2 200 Ma Silverton Formation close to the southernmost part of the Pilanesberg dyke swarm. The AIB has only been observed in cores from a borehole drilled close to Carletonville. It is hypocrystalline, containing randomly oriented elongated skeletal kaersutite crystals and 6 to 8 mm varioles mainly composed of radially oriented acicular plagioclase. These two textures are related to undercooling, probably linked to the limited thickness (70 cm) of the AIB coupled with a probable shallow emplacement depth. Ar-Ar dating of the kaersutite gives an age of ca. 1 400 Ma, similar to the age of Pilanesberg Complex. However, the AIB is an alkaline basaltic andesite and is thus notably less differentiated than the Pilanesberg Complex and some of its associated dykes, such as the Maanhaarrand dyke, for which we provide whole-rock geochemical data. Literature data indicate that the Pilanesberg dyke swarm also contains mafic hypabyssal rocks suggesting a link between the dyke swarm and the AIB. The AIB is characterized by strongly negative ?Nd and ?Hf, that cannot be related to crustal contamination, as shown by positive Ti and P anomalies, and the absence of negative Nb-Ta anomalies in mantle-normalised trace element diagrams. The AIB magma is interpreted to have been derived from a long-lived enriched, probably lithospheric mantle reservoir. The AIB thus provides important information on the magma source of the Pilanesberg Alkaline Province.
Lithos, doi.org/10.1016/ jlithos.2020.105880, 26p. Pdf
Africa, South Africa
deposit - Bultfontein
Abstract: The metasomatised continental mantle may play a key role in the generation of some ore deposits, in particular mineral systems enriched in platinum-group elements (PGE) and Au. The cratonic lithosphere is the longest-lived potential source for these elements, but the processes that facilitate their pre-concentration in the mantle and their later remobilisation to the crust are not yet well-established. Here, we report new results on the petrography, major-element, and siderophile- and chalcophile-element composition of native Ni, base metal sulphides (BMS), and spinels in a suite of well-characterised, highly metasomatised and weakly serpentinised peridotite xenoliths from the Bultfontein kimberlite in the Kaapvaal Craton, and integrate these data with published analyses. Pentlandite in polymict breccias (failed kimberlite intrusions at mantle depth) has lower trace-element contents (e.g., median total PGE 0.72 ppm) than pentlandite in phlogopite peridotites and Mica-Amphibole-Rutile-Ilmenite-Diopside (MARID) rocks (median 1.6 ppm). Spinel is an insignificant host for all elements except Zn, and BMS and native Ni account for typically <25% of the bulk-rock PGE and Au. High bulk-rock Te/S suggest a role for PGE-bearing tellurides, which, along with other compounds of metasomatic origin, may host the missing As, Ag, Cd, Sb, Te and, in part, Bi that are unaccounted for by the main assemblage. The close spatial relationship between BMS and metasomatic minerals (e.g., phlogopite, ilmenite) indicates that the lithospheric mantle beneath Bultfontein was resulphidised by metasomatism after initial melt depletion during stabilisation of the cratonic lithosphere. Newly-formed BMS are markedly PGE-poor, as total PGE contents are <4.2 ppm in pentlandite from seven samples, compared to >26 ppm in BMS in other peridotite xenoliths from the Kaapvaal craton. This represents a strong dilution of the original PGE abundances at the mineral scale, perhaps starting from precursor PGE alloy and small volumes of residual BMS. The latter may have been the precursor to native Ni, which occurs in an unusual Ni-enriched zone in a harzburgite and displays strongly variable, but overall high PGE abundances (up to 81 ppm). In strongly metasomatised peridotites, Au is enriched relative to Pd, and was probably added along with S. A combination of net introduction of S, Au +/? PGE from the asthenosphere and intra-lithospheric redistribution, in part sourced from subducted materials, during metasomatic events may have led to sulphide precipitation at ~80-120 km beneath Bultfontein. This process locally enhanced the metallogenic fertility of this lithospheric reservoir. Further mobilisation of the metal budget stored in these S-rich domains and upwards transport into the crust may require interaction with sulphide-undersaturated melts that can dissolve sulphides along with the metals they store.
Nature Scientific Reports, doi.org/10.1038/ s41598-020-76800-0 10p. Pdf
Australia, Africa, South Africa
alkaline magmatism
Abstract: Large-scale mantle convective processes are commonly reflected in the emplacement of Large Igneous Provinces (LIPs). These are high-volume, short-duration magmatic events consisting mainly of extensive flood basalts and their associated plumbing systems. One of the most voluminous LIPs in the geological record is the ~?2.06 billion-year-old Bushveld Igneous Complex of South Africa (BIC), one of the most mineralised magmatic complexes on Earth. Surprisingly, the known geographic envelope of magmatism related to the BIC is limited to a series of satellite intrusions in southern Africa and has not been traced further afield. This appears inconsistent with the inferred large size of the BIC event. Here, we present new radiometric ages for alkaline magmatism in the Archean Yilgarn Craton (Western Australia), which overlap the emplacement age of the BIC and indicate a much more extensive geographic footprint of the BIC magmatic event. To assess plume involvement at this distance, we present numerical simulations of mantle plume impingement at the base of the lithosphere, and constrain a relationship between the radial extent of volcanism versus time, excess temperature and plume size. These simulations suggest that the thermal influence of large plume events could extend for thousands of km within a few million years, and produce widespread alkaline magmatism, crustal extension potentially leading to continental break-up, and large ore deposits in distal sectors. Our results imply that superplumes may produce very extensive and diverse magmatic and metallogenic provinces, which may now be preserved in widely-dispersed continental blocks.
Earth and Planetary Science Letters, doi.org/10.1016/ j.epsl.2020. 116720 19p. Pdf
Africa, South Africa
deposit - Bellsbank
Abstract: The nature of the deep calcium geochemical cycle through time is unresolved, in part due to the dearth of information about the calcium isotope composition of Archean recycled oceanic crust. Remnants of such ancient oceanic crust are preserved in the form of cratonic mantle eclogites, brought to surface as xenoliths in kimberlite magma eruptions. The ? 44 / 40Ca of fresh mantle-derived eclogite xenoliths (i.e., garnet and omphacite mineral separates) from the Bellsbank kimberlite on the Kaapvaal craton in South Africa are presented here in combination with their trace element compositions, garnet Fe3+ contents and ?18O values. The studied Bellsbank eclogite xenoliths have geochemical compositions that indicate oceanic crustal protoliths, with bulk Al2O3 from 15 to 27 wt.%, Eu anomalies from 0.8 to 2.6 and, significantly, garnet ?18O values from +2.7 to +6.2‰. Garnet Fe3+/?Fe contents yield logfO2(?FMQ) values between -4.0 and -1.2 for a depth range of 110-180 km, recording strong redox heterogeneity of the eclogite component within the Archean Kaapvaal mantle lithosphere. Reconstructed bulk eclogite MgO contents correlate negatively with fO2, suggesting that the redox compositions are related to magmatic differentiation during oceanic crust formation, excluding secondary metasomatic overprints. These data may thus emphasize that Archean basaltic oceanic crust had a similarly variable redox composition to modern MORB-type crust. Reconstructed bulk ? 44 / 40Ca values for the Bellsbank eclogites range from +0.28 to +1.56‰. Although some of the xenoliths have ? 44 / 40Ca values that overlap with the average mantle composition and modern MORB (+0.94 ± 0.1 and +0.83 ± 0.05‰), half of our dataset shows excursions to more extreme Ca isotopic compositions. Both higher and lower ? 44 / 40Ca relative to mantle compositions are recorded by the eclogites, with a general negative correlation with ?18O suggestive of seawater-alteration of oceanic crust. The combined low ? 44 / 40Ca (+0.28‰) and ?18O (+3.4‰) measured for one eclogite xenolith may record a subtle imprint by carbonate-rich mantle melts, which are known to contain isotopically light calcium contributed by recycled sediments. In contrast, the high ? 44 / 40Ca of up to +1.56‰ for some eclogite xenoliths, coupled with strong LREE depletion, can be explained by calcium isotope fractionation during partial melting. The protracted history of recycled oceanic crust as probed by cratonic mantle eclogites is recorded by their highly variable ? 44 / 40Ca-?18O-fO2 signatures. Whereas some of this heterogeneity can be linked to processes that operated on the Archean ocean floor such as seawater-alteration of basaltic crust, other sources of compositional variability are introduced by loss and addition of melts during subduction recycling and mantle residence. The observed ? 44 / 40Ca complexity of ancient recycled oceanic crust components at the scale of a single mantle-derived eclogite xenolith suite implies that mantle plume sourced intraplate magmas should reveal similarly strong calcium isotope variations contributed by apparently essential recycled crust components - as observed in the global oceanic island basalt record.
Vancouver Kimberlite Cluster, Feb. 24, recorded update https://www.youtube.com/ channel/UCcZvayDnqDD azIHAh1Otreg gets you into the VKC
Africa, South Africa
deposit - Koffiefontein
Abstract: Diamonds and their mineral inclusions preserve mantle processes over space and time. Forming over a protracted period, diamonds also provide snapshots of early craton formation and mantle evolution over much of Earth’s history. The lithosphere beneath Koffiefontein is extremely depleted and is characterised by high-Mg# olivine and low-Ca garnet. In addition to garnet LREE enrichment, Koffiefontein experienced a unique K-Nb-Ta-rich metasomatism event that resulted in new minerals. The lack of clinopyroxene and co-existing garnet-orthopyroxene assemblages lead to the use of the electron microprobe for trace element analysis of Al in olivine. Geothermobarometry indicates that upper mantle diamond formation conditions are 1100-1300 °C and 4-7 GPa. Koffiefontein diamonds have a main ?13C mode for both peridotitic and eclogitic diamonds similar to mantle carbon. Relationships of ?15N-[N] and ?13C-?15N indicate that nitrogen was derived from subducted sources and suggests that formation of not only eclogitic but also peridotitic diamonds involved fluids derived from altered oceanic crust. Lower mantle diamonds with coexisting ferropericlase and former bridgmanite indicate formation at or below 660 km. The high bulk Mg# of this assemblage is consistent with the diamond substrate originating from the depleted lithospheric mantle portion of an oceanic slab. Diamond formation at Koffiefontein dominantly takes place in depleted peridotite at both lithospheric and lower mantle depths. The ?13C-?15N systematics suggest the same subducted source for both peridotitic and eclogitic diamonds. Subduction has played an important role in the formation and evolution of the Kaapvaal Craton and subsequent diamond formation.
Abstract: Thirty-nine garnet harzburgites from Kimberley in the Kaapvaal Craton (South Africa) were studied to constrain the origin, age and evolution of sub-cratonic lithospheric mantle (SCLM). In order to avoid chemical overprinting by recent metasomatism, only garnet harzburgites that appeared clinopyroxene-free to the naked eye were sampled. The majority of garnets were, however, in equilibrium with clinopyroxene (24 of 39). Whole rock and mineral major-trace element geochemistry and garnet Sr-Nd-Hf isotope data are presented. Equilibration pressures range from 3.8-6.1?GPa, indicating the harzburgites were derived from a large portion of the SCLM (~115-185?km). High olivine Mg# (~93.4, n?=?39) and low whole rock heavy rare earth elements (HREE) contents are consistent with large degrees of partial melting (>45%) and garnet exhaustion leaving a dunitic residue with olivine ?90%, orthopyroxene ?10% and HREE <0.01 times chondrite. Mineral modes, whole rock Al2O3 (0.5-3.2?wt%) and SiO2 (43.1-49.1?wt%), however, indicate heterogeneous re-introduction of garnet (?13%) and orthopyroxene (?50%). Harzburgites with high garnet and relatively low orthopyroxene modes (mostly ~7-13% and?~?9-30%; n?=?6) are characterised by mildly sinusoidal garnet REE patterns (Tbsingle bondDy minimum and high HREE) and Archaean depleted Hf TDM ages (2.7-3.3?Ga; ?Hfe: +190 to +709). In contrast, harzburgites with high orthopyroxene and relatively low garnet and modes (~1.5-7.5% and?~?25-50%; n?=?19) are characterised by highly sinuous REE patterns (Hosingle bondYb minimum and low HREE) and Proterozoic enriched Hf TDM ages (0.7-1.6?Ga; ?Hfe: ?16 to +6). It is inferred that Archaean G10 garnet re-introduction caused a significant increase in HREE, making melt depletion models based on HREE inaccurate. Orthopyroxene addition, a few hundred million years later, most likely at ~2.7?Ga and associated with Ventersdorp magmatic activity, caused partial consumption of garnet and olivine, and changed garnet compositions leading to: 1) Cr/Al ratio increase; 2) HREE decrease; 3) more sinusoidal REE patterns; and 4) un-radiogenic 176Hf/177Hf. Garnets define a Lusingle bondHf isochron age of 2702?±?64?Ma (?Hfi?=?+44, n?=?31), which is interpreted as a consequence of partial isotopic equilibrium within the SCLM and mixing of the garnet- and orthopyroxene-rich metasomatic components. The low LILE contents and absence of Nbsingle bondTa anomalies are consistent with modal metasomatism caused by intra-plate magmatism. In addition, the REE signatures of metasomatic agents in equilibrium with the garnets suggest that carbonatitic melts and SiO2-rich hydrous melts were responsible for re-introduction of garnet and orthopyroxene, respectively. Srsingle bondNd isotope systematics were disrupted associated with kimberlite magmatism (Nd isochron: 217?±?58?Ma, ?Ndi?=?+4; n?=?34), consistent with recent G10 garnet transformation into G9 garnets (Ca?+?Fe-enriched). This event may have caused garnet addition (up to 1%), suggesting that garnet was formed or destroyed in at least 4 different events: i) initial extensive polybaric melting, ii) asthenospheric melts re-introducing the bulk of the garnet, iii) orthopyroxene addition and garnet loss, all in the Archaean, and iv) minor garnet addition possibly related to recent kimberlite magmatism prior to eruption.
Abstract: Samples from three petrographically distinct, intrusive kimberlite bodies and associated kimberlite dykes from the eastern lobe of the Du Toitspan kimberlite pipe, Kimberley, South Africa, have been analysed for their bulk rock major and trace element compositions and their olivine and phlogopite compositions. The two dominant intrusive bodies (D13, D14) are distinguished by the one (D13) being phlogopite-rich and best classified as a macrocrystic hypabyssal phlogopite kimberlite, and the other (D14) being phlogopite-poor and best classified as a macrocrystic hypabyssal monticellite kimberlite. The minor D17 intrusive body is classified as a macrocrystic transitional hypabyssal serpentinized phlogopite kimberlite. The associated kimberlite dykes range texturally from aphanitic to macrocrystic and are classified as calcite kimberlites. The major kimberlite intrusions and their associated dykes show no evidence of crustal contamination and are characterised by broadly overlapping geochemistry except for distinctly higher K2O (> 2?wt%) and Al2O3 (>3?wt%) and flattening HREE patterns (Gd/YbN?=?6.5-7.0) in the D13 - phlogopite kimberlite compared to the D14 - monticellite kimberlite and the calcite kimberlite dykes (Gd/YbN?=?9.6-12.1). These distinguishing geochemical features of the D13 - phlogopite kimberlite are comparable to typical Group II kimberlites in southern Africa. However, their diagnostic incompatible trace element ratios (for example, Th/Nb, La/Nb, Ce/Pb, and Ba/Nb) are instead comparable to other kimberlite intrusions analysed in this study and to southern African Group I kimberlites in general. Semi-quantitative modelling suggests that these kimberlite intrusions could have derived by low (<1%) degrees of partial melting of a source region that is enriched in LREE (Lan?=?~6.1; Ybn?~?1.47) comparable to metasomatised peridotites from the underlying lithospheric mantle. The composition of the D13 phlogopite kimberlite is consistent with a partial melt of a modally metasomatised source containing a higher proportion of residual clinopyroxene relative to garnet (compared to that giving rise to the D14 monticellite kimberlite and calcite kimberlite dykes), as well as accessory amounts of phlogopite, i.e. a garnet phlogopite peridotite (GPP). The absence of K-anomalies on primitive mantle normalized diagrams for the D13 phlogopite kimberlite requires that phlogopite was not a residual phase during partial melting and was exhausted shortly before or at the moment of melt segregation. The higher Gd/Yb ratios and lower K2O in the D14 monticellite kimberlite and calcite kimberlite dykes can be explained by partial melting of a cryptically metasomatized, phlogopite - free, garnet peridotite (GP) source, containing a higher proportion of garnet relative to clinopyroxene. The low absolute K and strong negative K-anomaly on primitive mantle normalized diagrams for the D14 monticellite kimberlite were inherited from a source region that previously experienced cryptic metasomatism by a differentiated fluid already carrying a negative K-anomaly.
Abstract: The paper brings together the language of diamond numbers and the underlying principles for calculation of diamond liberation, followed by estimation of process efficiency at circuit and complete plant levels. In this way it provides a reference point, albeit a mixture of the theoretical and empirical, to assess the effectiveness of diamond plant accounting systems in the field. Having established today's baseline, the wider aim is ongoing education, peer technical debate, and progression to a more exact science.
Abstract: Investing in a mining venture can be risky and stakeholders need transparent, unbiased reports to understand the Mineral Resources and Mineral Reserves a mining company holds. Readability and textual choice can be used consciously to manipulate perceptions, or it can be done unconsciously. This exploratory study investigates the readability and textual choice of supplementary Mineral Resources and Mineral Reserves Reports of companies listed on the Johannesburg Stock Exchange. The results indicate that narrative manipulation occurs in these reports through word choices that make the reports difficult to read, as well as specific narrative selections. This reduces the informational value of the reports. The results of the study will be useful to various stakeholders, such as mining company management, investors, investment specialists, financial analysts, and even employees and the general community, who all use these reports to make important decisions. It is also useful for the preparers of the Mineral Resources and Mineral Reserves Reports, Competent Persons, and other technical specialists to be aware of readability and that certain textual choices can affect the interpretation of these reports. It is recommended that bodies such as the JSE and the SAMREC and SAMVAL Code committees consider adding a plain language requirement to regulations, guidelines, and codes to ensure transparent, unbiased, and objective reports.
Journal of Geochemical Exploration, Vol. 224, 106757, 13p. Pdf
Africa, South Africa
deposit - Palabora
Abstract: A detailed characterization of alkaline tailing ponds and waste rock dumps from Phalaborwa Igneous Complex (PIC) South Africa, has been accomplished. The study goes beyond the environmental characterization of mining wastes, offering the first insight towards the recycling of the wastes as alkaline reagent to neutralize acid industrial wastewater. To achieve these aims, tailings and waste rocks were characterized using a combination of conventional, novel and modified Acid Rock Drainage (ARD) prediction methodologies, as well as South African leachate tests, sequential extractions and pseudo-total digestions. The scarcity of Fe-sulphide minerals and the abundance of alkaline minerals indicated that PIC wastes are not ARD producers. The highest neutralization potential was found in the carbonatite rocks and East tailing samples (range between 289 and 801 kg CaCO3 eq/t). According to the National Environmental Management Waste Act (59/2008) of South Africa, tailing ponds and waste rock dumps from PIC classify as non-hazardous (Type 3 waste). The sequential extractions showed that the different fractions from most of the samples would mostly release sulphate and non-toxic elements, such as Ca, Mg, Na and K, which might be a concern if leached in high concentration. In addition, relatively high concentrations of radionuclides, such as U and Th (average of 6.7 and 36.3 mg/kg, respectively) are present in the non-labile fraction of PIC wastes, while the leachable concentrations were always below 0.006 mg/L. Among PIC wastes, East tailing would be the best option as alkaline reagent to neutralize acid wastewater because of its high neutralization potential and non-harmful leachate composition. In general, this study exposes the shortcomings in mine waste characterization, particularly for alkaline mine wastes, and introduces the assessment of potential revalorization as a novel practice in mine waste characterization that, if extended as a regular practice, would facilitate a circular economy approach to the mining industry with its consequent economic and environmental benefits.
Abstract: Projects with long histories must be documented in current disclosures with transparency and materiality, using historical data and historical estimates. Historical data may be of great value if it is from a reliable source, and the raw data can be validated and/or duplicated. Historical estimates can and should be reported, but with qualification of the ever-changing economic parameters of ‘Reasonable Prospects for Eventual Economic Extraction’ (RPEEE). The SAMREC Code requires current sampling results and diamond valuations, without which RPEEE cannot be assessed; consequently, historical estimates cannot ever be declared as current Diamond Resources or Reserves. The SAMREC Code defines historical estimates and provides guidance on the use of historical data. Examples from real projects and reports in the public domain are reviewed in this paper. Opinions on use and misuse are those of the writer; judgment on good or bad practice is not the intention and is left to the opinion of the reader. Comparison, with both the JORC Code (Australasia) and CIM Definition Standards and National Instrument 43-101 (Canada), is provided. The SAMREC Code appears to be more closely aligned with the Canadian standards.
Abstract: Alluvial diamond and other gemstone deposits have, typically, been exploited by small artisanal operations with little or no geological control. Over the last decade, however, alluvial deposits have become more interesting to larger (often listed), mid-tier companies wishing to benefit from the higher incomes generated by high-quality stones. The difficulties associated with evaluation and valuation of such alluvial diamond/gemstone deposits are widely known but, regrettably, often not widely understood - leading to several misconceptions over what can and cannot be expected from such deposits. Fortunately, there is a reasonably well-established body of knowledge on alluvial diamonds that has resulted in accepted industry-standard practices of how to evaluate these deposits. The 2016 version of the SAMREC Code includes several sections specific to the requirements of secondary diamond and gemstone deposits, both alluvial and marine. Consequently, it is possible to define Diamond/Gemstone Resources in accordance with the major international Committee for Mineral Reserves International Reporting Standards (CRIRSCO) type codes. This paper outlines some of the requirements and some of the pitfalls that need to be appreciated while estimating Diamond/Gemstone Resources and/or Reserves on such deposits.
Abstract: Chemical events involving deep carbon- and water-rich fluids impact the continental lithosphere over its history. Diamonds are a by-product of such episodic fluid infiltrations, and entrapment of these fluids as microinclusions in lithospheric diamonds provide unique opportunities to investigate their nature. However, until now, direct constraints on the timing of such events have not been available. Here we report three alteration events in the southwest Kaapvaal lithosphere using U-Th-He geochronology of fluid-bearing diamonds, and constrain the upper limit of He diffusivity (to D???1.8?×?10?19 cm2 s?1), thus providing a means to directly place both upper and lower age limits on these alteration episodes. The youngest, during the Cretaceous, involved highly saline fluids, indicating a relationship with late-Mesozoic kimberlite eruptions. Remnants of two preceding events, by a Paleozoic silicic fluid and a Proterozoic carbonatitic fluid, are also encapsulated in Kaapvaal diamonds and are likely coeval with major surface tectonic events (e.g. the Damara and Namaqua-Natal orogenies).
South African Journal of Geology, doi:10.25131/sajg.124.0028 10p. Pdf
Africa, South Africa
deposit - Salpeterkop
Abstract: The Salpeterkop volcano forms part of what has been referred to as the Upper Cretaceous Sutherland Suite of alkaline rocks, an igneous province composed of olivine melilitites, carbonatites, trachytes and ultramafic lamprophyres. Salpeterkop is a remnant of the summit tuff ring structure that surrounds a crater which is almost 1 km in diameter and is filled with epiclastic strata. Five pieces of silicified wood were collected from the crater filled sediments, sectioned and identified as a new species of Cupressinoxylon, C. widdringtonioides. This is the first example of the fossil genus in South Africa. Only one member of the Cupressaceae s.l. occurs in southern Africa today. From the wide and indistinct growth rings in the fossil wood it can be deduced that the local climate was warm and humid with little or no seasonality, in support of global records of a warm Late Cretaceous. The preservation of the crater further signifies the low level of erosion the region has experienced since its emplacement.
Abstract: Thermal events and metasomatic processes have influenced the Kaapvaal craton in South Africa. High-density fluids (HDFs) trapped as microinclusions in diamond are main metasomatic agents which provide an insight to these processes in the Earth's mantle. Here we present data for 15 fibrous, HDF-bearing diamonds from the Voorspoed mine, South Africa, reflecting multiple diamond-forming events in a cooling lithosphere. Analyzed by FTIR and EPMA, the Voorspoed fibrous diamonds reveal three populations that differ in their nitrogen aggregation and HDF composition. A silicic?carbonatitic group containing 11-30% B-centers, a saline group containing 5-16% B-centers, and a single high-Mg carbonatitic diamond with 0% B-centers. The distinct nitrogen aggregation of the fibrous diamond groups in Voorspoed and the lack of clear major element evolutionary trends for each HDF type or intermediate compositions between the different types suggest different time-temperature formation histories. Thermobarometry of mineral inclusions in non-fibrous monocrystalline Voorspoed diamonds (Viljoen et al., 2018) indicates that the Voorspoed lithosphere cooled by 100-200 °C since their host diamonds crystallized at high initial temperatures. High temperatures in Voorspoed lithosphere can be correlated with the eruption of the Ventersdorp flood basalts at the central Kaapvaal (ca. 2.7 Ga) or the Bushveld complex (ca. 2.06 Ga), and cooling rates of the lithosphere provide a time frame for a cooling process that originated ~2-3 Ga. Combining these data with the nitrogen aggregation systematics of fibrous and monocrystalline Voorspoed diamonds, we suggest that most Voorspoed diamonds formed during 4 metasomatic events: the oldest one recorded took place between 2 and 3 Gyr as a result of a major thermal perturbation, whereas the following three occurred between 200 and 600 Myr, 30-90 and < 30 Myr before kimberlite eruption in a cooling lithosphere. An even older (or deeper) event is hinted by a few diamonds where all nitrogen is in B-centers. The sequence of events implied by Voorspoed HDF compositional and nitrogen aggregation differences show affinities with other occurrences in South Africa (e.g. Kimberley, Finsch and Koffiefontein) and may reflect thermal and lithological variation between the central and southwest Kaapvaal lithosphere.
Le Bras, L.Y., Bolhar, R., Bam, L., Guy, B.M., Bybee, G.M., Nex, P.A.M.
Three dimensional tectural investigation of sulfide mineralisation from the Loolekop carbonatite-phoscorite polyphase intrusion in the Phalaborwa Igneous Complex ( South Africa), with implications for ore-forming processes.
Mineralogical Magazine, 19p. Pdf doi:10.1180/mgm.2021.32
Abstract: Controversies surround the origin of kimberlite megacrysts, including whether and how they are genetically related to their host kimberlites, the relationship between the Cr-poor and Cr-rich suites and the dominant processes responsible for elemental and isotopic variations of megacrysts from a given kimberlite. We present new in-situ major and trace element and Sr isotopic results for clinoyroxene and garnet megacrysts from four southern African kimberlites: Colossus and Orapa (Group 1 kimberlites on the Zimbabwe craton), and Kalkput and Bellsbank (Group 2 kimberlites on the western Kaapvaal craton), that include both Cr-poor and Cr-rich megacryst varieties. Cr-poor megacrysts are present at Colossus, Orapa and Kalkput and the data exhibit tight, well-defined trends on major element diagrams as well as incompatible and rare earth element abundances similar to those previously reported for Cr-poor megacrysts. Cr-rich megacrysts, which are also present at Orapa and are the only variety present at Bellsbank, generally have higher Mg# values, lack well-defined major element trends and show stronger incompatible element enrichments as well as more radiogenic 87Sr/86Sri ratios than Cr-poor megacrysts from the same kimberlite group. Thermobarometry indicates that the Cr-poor megacrysts equilibrated at temperatures of ?1200 to 1450 °C and pressures of 4.5 to 7.5 GPa. Cr-rich megacrysts, in contrast, extend to temperatures and pressures as low as 700 °C and 3 GPa, respectively. This indicates that, in the studied suites, Cr-poor megacrysts equilibrated at high temperatures in the lower lithosphere (>135 km), whereas Cr-rich megacrysts typically equilibrated at lower temperatures and pressures. Within the Cr-poor megacrysts from Group 1 and Group 2 kimberlites, there is a clear correspondence between kimberlite group, diagnostic incompatible element ratios (e.g., Nb/La) and Sr isotope ratios that parallel the differences noted between whole-rock Group 1 and Group 2 kimberlites. In the case of Cr-poor megacrysts, similar calculated melt compositions in equilibrium with garnet and clinopyroxene from the same kimberlite were obtained using recent high-pressure mineral?carbonated melt partition coefficients. This suggests formation in conditions close to trace element equilibrium, and is consistent with crystallization from primitive melts with kimberlite-like trace element compositions. In the case of Cr-rich megacrysts, differences in the compositions of melts in equilibrium with clinopyroxene and garnet tend to be larger, and melts in equilibrium with Cr-rich clinopyroxene tend to show significantly greater incompatible element enrichments than those of estimated near-primary kimberlite melts. This could be due to the different behaviour of clinopyroxene and garnet during metasomatic melt-rock interaction, but the apparent disequilibrium between clinopyroxene and garnet could also be due to some of the Cr-rich megacrysts actually being peridotitic xenocrysts. We propose a model for the origin of southern African megacrysts in which carbonated protokimberlite melts formed stockwork-like bodies of variable size in the deep lithosphere (>130 km), which fed networks of melt-filled veins extending into the surrounding and overlying mantle. Crystallization of larger melt bodies resulted in megacryst assemblages dominated by Cr-poor megacrysts, and the incompatible element and isotopic characteristics of these dominantly reflect those of the protokimberlite melt. In contrast, crystallization of smaller melt bodies and their vein networks resulted in megacryst assemblages dominated by Cr-rich megacrysts, which formed as a result of extensive assimilation and metasomatic melt-rock interaction between protokimberlite and peridotite wallrock at low melt/rock ratios, particularly in the middle to shallow lithosphere where pre-existing potassic metasomatic heterogeneities are prevalent. The Cr-rich nature and enrichments in incompatible elements and radiogenic Sr in the Cr-rich megacrysts reflect extensive interaction of their parental magmas with this metasomatized peridotite.
AGU Research Letter, 10.1029/2021GL092570 11p. Pdf
Africa, South Africa
geophysics - magnetotellurics
Abstract: Measuring the composition of the Earth’s mantle is important for understanding mantle processes like plate tectonics, but is surprisingly difficult. Our most accurate information comes from mantle rocks, called xenoliths, that have been brought to the surface during volcanic eruptions. However, these rocks only come from a handful of places. We tend to expect that the rest of the mantle has the same composition as the xenoliths but this might be incorrect. We tested whether xenolith compositions really are representative of the broader mantle by comparing them with compositions interpreted from electrical conductivity models of the mantle. We carried out this comparison in the Kimberley region, South Africa, because it has excellent xenolith and electrical conductivity data. Our results show that xenolith compositions do seem to be broadly representative but there are two important differences: Hydrous minerals found in some xenoliths may not be spatially extensive depending on temperature, and the water contents of some other minerals are different from the broader region. This means that the compositions of xenoliths are at least partly controlled by local processes. Electrical conductivity data may be more useful for measuring some aspects of the composition of the broader mantle, especially its water content.
Journal of Gems & Precious Metals, Vol. 1, 1 pp. 1-11. pdf
Africa, South Africa
deposit - Loxtondal
Abstract: At the end of 2014, around the so called Loxtondal Orangeitic (now called Kaapval type lamproites) cluster, in Boshof district, two circular a nomalies (~540 to ~1100 meters in diameter) were identified by Landsat Satellite Images and interpreted as being of "kimberlites" pipes; probable anomaly which were referred to as Olie 1 and Olie 2. Subsequently, 100 kg of soil samples (horizon A/B) were taken for each of these anomalies. From them there was a high concentration of indicator minerals (IM): olivine, garnets (violets, reds and oranges), chromites, ilmenites, rutile, frosting tourmaline, zircon and among them some crystals of micro and macro diamonds. The high concentration of IM on Olie 2 led to focus the work on it . IM of Olie 2 was burned in HFl and by caustic fusion what contributed about 86 macro (<1 mm) and micro diamonds. The previus works contributed to raising the interest of some diamond geology groups that took new samples that provided electron microprobe analysis of hundreds of chromites and hundreds of garnets: chromites; picro-cromites, and G-9-G-10 garnets. The calculated pressure of the formation of chromites and garnets of Oli e 2 released in the information of seismic Vs-1D and tomography (Model TX2011). It would allow more adequately to reproduce these two minerals generated in the facies of diamonds and separate them from those generated in facies of graphite. A task that would allow a better approach to the diamond potential of this anomaly studied. It was found that in Olie 2 chromites of diamond facies and garnets (G 9 and G 10) are very representative. For this time the study of the lithospheric cratonic mantle (Archon), through of the commented seismic Vs-1D and tomography (Model TX2011) on the Loxtondal cluster (Olie-2)/Kimberley-area setting allowed to estimate the surface heat flow as being approximately 37.5 mW/m2 = 280 km depth of cratonic root (or LAB). Environment in which the highest reference diamond grade is the Kimberley pipe with 200 cpht; and so, for this reason, a similar diamonds-grade could be expected on the Olie-2/potential associated pipes-area.
Abstract: The central region of the Kaapvaal craton is relatively understudied in terms of its lithospheric mantle architecture, but is commonly believed to be significantly impacted by post-Archean magmatism such as the ca. 2056 Ma Bushveld large igneous event. We investigate a collection of 17 eclogite xenoliths from the Cretaceous Palmietfontein kimberlite at the Western Limb of the Bushveld Complex for their mineralogical compositions (major and trace elements, plus Fe3+ contents), as well as stable oxygen and radiogenic Pb isotopic compositions to gain further insights into the nature and evolution of the central Kaapvaal cratonic mantle lithosphere. New U/Pb age determinations on mantle-derived zircon yield a magma emplacement age of ca. 75 Ma for the Palmietfontein Group-1 kimberlite, which means that the entrained eclogite xenoliths may record a protracted metasomatic history from the Proterozoic through to most of the Phanerozoic eon. Garnet ?18O values of up to 6.9‰ and positive Eu anomalies for the bulk rocks suggest seawater-altered oceanic crustal protoliths for the Palmietfontein eclogite xenolith suite, which is typical for the eclogitic components of the Kaapvaal root and other cratonic mantle sections worldwide. However, several features of the Palmietfontein eclogites are commonly not observed in other mantle-derived eclogite xenolith suites. Firstly, the samples studied yield relatively low equilibration pressures and temperatures between 2.7 and 4.5 GPa and 740-1064 °C, indicating a relatively shallow residence between 90 and 150 km depths. Secondly, euhedral coarse amphibole is present in several eclogite nodules where it is in equilibrium with ‘touching’ garnet, supporting eclogite residence within the amphibole stability field at uppermost lithospheric mantle conditions. Thirdly, primary omphacitic clinopyroxene is often overgrown by diopside, and is significantly enriched in incompatible trace elements. The clinopyroxene is also characterized by elevated 206Pb/204Pb of 17.28-19.20 and 207Pb/204 Pb of 15.51-16.27, and these Pb isotopic compositions overlap with those of Mesozoic Group-2 kimberlites from the Kaapvaal craton. Our results show that eclogites reside at ~85 km depth beneath the central Kaapvaal craton as part of a layer that corresponds to an approximately 50 km thick seismically-detected mid-lithospheric discontinuity. Mid-lithospheric discontinuities have been interpreted as metasomatic fronts formed by focussed crystallization of hydrous mineral phases from enriched volatile-bearing melts, and as such the strongly overprinted amphibole-bearing eclogite xenoliths from Palmietfontein may represent a physical expression of such seismically anomalous metasomatic layer at mid-lithospheric depth. Our Pb isotope data suggest that the focussed metasomatism can be attributed to volatile-rich melts reminiscent of potassic Group-2 kimberlites, which have been invoked in MARID-style metasomatic overprinting of the lower lithospheric mantle beneath the western Kaapvaal craton. However, the relatively low fO2 recorded by the Palmietfontein eclogites (minimum FMQ-4.5) suggests that the metasomatism at mid-lithospheric depth was less protracted compared to the more intensive and oxidizing metasomatism typically observed near the base of cratonic mantle roots. While it is possible that Proterozoic magmatic events were responsible for the focussed mid-lithospheric metasomatism of the Kaapvaal mantle, on the basis of the Pb isotope constraints the Palmietfontein eclogites were most likely overprinted during ca. 120 Ma Group-2 kimberlite magmatism.
Tappe, S., Massuyeau, M. , Smart, K.A., Woodland, A.B., Gussone, N., Milne, S., Stracke, A.
Sheared peridotite and megacryst formation beneath the Kaapvaal Craton: a snapshot of tectonomagmetic processes across the lithosphere-asthenosphere transition.
Geological Society of London Special Publications, doi:https://dori.org/10.1144/SP513-2021-84 30p. Pdf proof
Africa, South Africa
lamproite
Abstract: Orangeites are a significant source of diamonds, yet ambiguity surrounds their status among groups of mantle-derived potassic rocks. This study reports mineralogical and geochemical data for a ca. 140 Ma orangeite dyke swarm that intersects the Bushveld Complex on the Kaapvaal craton in South Africa. The dykes comprise distinctive petrographic varieties that are linked principally by olivine fractionation, with the most evolved members containing minor amounts of primary carbonate, sanidine and andradite garnet in the groundmass. Although abundant groundmass phlogopite and clinopyroxene have compositions that are similar to those of cratonic lamproites, these phases show notable Ti-depletion, which we consider a hallmark feature of type orangeites from the Kaapvaal craton. Ti-depletion is also characteristic for the bulk rock compositions and is associated with strongly depleted Th-U-Nb-Ta contents at high Cs-Rb-Ba-K concentrations. The resultant high LILE/HFSE ratios of orangeites suggest that mantle source enrichment occurred by metasomatic processes in the proximity of ancient subduction zones. The Bushveld-intersecting orangeite dykes have strongly enriched Sr-Nd-Hf isotopic compositions (initial 87Sr/86Sr = 0.70701-0.70741; ?Nd = ?10.6 to ?5.8; ?Hf = ?14.4 to ?2.5), similar to those of other orangeites from across South Africa. Combined with the strong Ti-Nb-Ta depletion, this ubiquitous isotopic feature points to the involvement of ancient metasomatized mantle lithosphere in the origin of Kaapvaal craton orangeites, where K-rich metasomes imparted a ‘fossil’ subduction geochemical signature. Previous geochronology studies identified ancient K-enrichment events within the Kaapvaal cratonic mantle lithosphere, possibly associated with collisional tectonics during the 1.2-1.1 Ga Namaqua-Natal orogeny of the Rodinia supercontinent cycle. It therefore seems permissible that the cratonic mantle root was preconditioned for ultrapotassic magma production by tectonomagmatic events that occurred along convergent plate margins during the Proterozoic. However, reactivation of the K-rich metasomes had to await establishment of an extensional tectonic regime, such as that during the Mesozoic breakup of Gondwana, which was accompanied by widespread (1000 × 750 km) small-volume orangeite volcanism between 200 and 110 Ma. Although similarities exist between orangeites and lamproites, these and other potassic rocks are sufficiently distinct in their compositions such that different magma formation processes must be considered. In addition to new investigations of the geodynamic triggers of K-rich ultramafic magmatism, future research should more stringently evaluate the relative roles of redox effects and volatile components such as H2O-CO2-F in the petrogeneses of these potentially diamondiferous alkaline rocks.
South African Journal of Geology, Vol. 124, pp. 421-442.
Africa, South Africa
magmatism
Abstract: At least four spatially overlapping Large Igneous Provinces, each of which generated ~1 x 106 km3 or more of basaltic magmas over short time intervals (<5 m.y.), were emplaced onto and into the Kaapvaal Craton between 2.7 and 0.18 Ga: Ventersdorp (2 720 Ma, ~0.7 x 106 km3), Bushveld (2 056 Ma, ~1.5 x 106 km3), Umkondo (1 105 Ma, ~2 x 106 km3) and Karoo (182 Ma, ~3 x 106 km3). Each of these has been suggested to have been derived from melting of sub-continental lithospheric mantle (SCLM) sources, but this is precluded because: (1) each widespread heating event sufficient to generate 1 to 2 x 106 km3 of basalt from the Kaapvaal SCLM (volume = 122 to 152 x 106 km3) would increase residual Mg# by 0.5 to 2 units, depending on degree of melting, and source and melt composition, causing significant depletion in already-depleted mantle, (2) repeated refertilization of the Kaapvaal SCLM would necessarily increase its bulk density, compromising its long-term buoyancy and stability, and (3) raising SCLM temperatures to the peridotite solidus would also have repeatedly destroyed lithospheric diamonds by heating and oxidation, which clearly did not happen. It is far more likely, therefore, that the Kaapvaal LIPs were generated from sub-lithospheric sources, and that their diverse geochemical and isotopic signatures represent variable assimilation of continental crustal components. Combined Sr and Nd isotopic data (n = 641) for the vast volumetric majority of Karoo low-Ti tholeiitic magmatic products can be successfully modelled as an AFC mixing array between a plume-derived parental basalt, with <10% of a granitic component derived from 1.1 Ga Namaqua-Natal crust. Archaean crustal materials are far too evolved (?Nd ~ -35) to represent viable contaminants. However, a very minor volume of geographically-restricted (and over-analysed) Karoo magmas, including picrites, nephelinites, meimechites and other unusual rocks may represent low-degree melting products of small, ancient, enriched domains in the Kaapvaal SCLM, generated locally during the ascent of large-volume, plume-derived melts. The SCLM-derived rocks comprise the well-known high-Ti (>2 to 3 wt.% TiO2) magma group, have ?Nd, 182 values between +10.5 and -20.9, and are characteristically enriched in Sr (up to 1 500 ppm), suggesting a possible connection to kimberlite, lamproite and carbonatite magmatism. These arguments may apply to continental LIPs in general, although at present, there are insufficient combined Sr + Nd isotopic data with which to robustly assess the genesis of other southern African LIPs, including Ventersdorp (n = 0), Bushveld (n = 55) and Umkondo (n = 18).
South African Journal of Geology, Vol. 124, pp. 519-536.
Africa, South Africa
geodynamics
Abstract: The delicate interplay of various Earth’s systems processes in the Critical Zone is vital in ensuring an equilibrium across the different spheres of life. The upper crust forms a thin veneer on the Earth’s surface that is defined by an interconnected network of brittle structures. These brittle structures enable various Earth System processes. Increased anthropogenic interactions within the very upper crust have seemingly resulted in a growing number of negative natural effects, including induced seismicity, mine water drainage and land degradation. Brittle structures across South Africa are investigated. These structures include various fractures and dykes of different ages and geodynamic evolutions. The orientation of these structures is compared to the underlying tectonic domains and their bounding suture zones. The orientations corroborate an apparent link between the formation of the brittle structures and the tectonic evolution of the southern African crust. Reactivation and the creation of new structures are also apparent. These are linked to the variability of the surrounding stress field and are shown to have promoted magmatism, e.g., Large Igneous Provinces, and the movement of hydrothermal fluids. These fluids were commonly responsible for the formation of important mineral deposits. The preferred structural orientations and their relationship to underlying tectonic zones are also linked to fractured groundwater aquifers. Subsurface groundwater displays a link to structural orientations. This comparison is extended to surficial water movement. Surface water movement also highlights an apparent link to brittle structures. The apparent correlation between these Earth’s systems processes and the interconnectivity developed by brittle structures are clear. This highlights the importance of high-resolution geological and structural mapping and linking this to further development of the Earth’s Critical Zone.
Abstract: The Small and Junior diamond mining industry, which is dominated by alluvial diamond miners, and a few remaining small kimberlite operations, produced a high proportion of diamonds in South Africa in the late 1950s and early 1960s, prior to the discovery and development of major kimberlite mines such as Finsch and Venetia, in the 1970’s and 80’s. Subsequent to these discoveries the Small and Junior sector remained an active and important participant in the local diamond industry, particularly in respect of the highly sought after top-quality gemstone diamonds produced from the extensive alluvial deposits of South Africa. Since 2004 the sector has shown a strong decline. This report highlights the challenges faced by the Small and Junior diamond miners and makes recommendations for the revival of this sector.
The impact of the mineral and petroleum resources development act, ACT 28 of 2002 ( MPRDA) on th sustainability of the alluvial diamond mining sector in the northern Cape Province.
Abstract: Copper-sulfides within carbonatites and phoscorites of the Phalaborwa Igneous Complex, South Africa, have been investigated since the middle of the 20th Century. However, aspects of ore formation have remained unclear. This study examines the mechanisms involved in Cu-sulfide mineralisation by micro-focus X-ray computed tomography as applied to sulfide-rich drill core samples. Several texturally distinct assemblages of magmatic sulfides can be identified, including: (1) <500 ?m rounded bornite and chalcopyrite grains disseminated within the gangue; (2) elongated mm-scale assemblages of chalcopyrite and bornite; and (3) mm-to-cm thick chalcopyrite cumulates. Chalcopyrite veins were also observed, as well as late-stage valleriite, documenting late-stage fluid circulation within the pipe, and alteration of magmatic and hydrothermal sulfides along fractures within the gangue, respectively. The results of micro-focus X-ray computed tomography indicate that magmatic sulfides are sub-vertically aligned. Spatial variability of the sulfide assemblages suggests that textural changes within sulfide layers reflect fluctuating magma flow rate during emplacement of carbonatite-phoscorite magmas, through coalescence or breakup of sulfide liquid droplets during ascent. Modal sulfide abundances, especially for disseminated assemblages, differ from one carbonatite-phoscorite layer to another, suggesting a strong control of the mechanical sorting in the formation of Cu-sulfide textures within the Loolekop carbonatite. The alternation of carbonatite and phoscorite within the intrusion suggest that the Loolekop Pipe was emplaced through a series of successive magma pulses, which differentiated into carbonatite and phoscorite by melt immiscibility/progressive fractional crystallisation and pressure drop. Three-dimensional textural analysis represents an effective tool for the characterisation of magma flow and is useful for the understanding of magmatic processes controlling sulfide liquid-bearing phoscorite-carbonatite magmas.
Abstract: Models for a xenocryst origin for kimberlite olivines emphasise the similarity between their core compositions and those in mantle peridotites. While this permits a xenocryst origin, it does not provide proof, as magmas generated in equilibrium with mantle olivines could, in principle, crystallize initial olivines matching those in the source region. Further, in several kimberlites, there is a striking disparity between the compositional range of olivine cores and that in associated mantle peridotite xenoliths from the same locality. Olivine-liquid Mg-Fe exchange coefficients and Ni partition coefficients permit equilibrium between Mg-rich mantle olivines (Mg#?~?94-93) and magmas matching kimberlite bulk rock compositions. Glass inclusions in olivine megacrysts from the Monastery kimberlite, with compositions which overlap the range of archetypal Group I kimberlites, were interpreted to represent original liquids trapped at pressures of 4.5-6?GPa. These glass inclusions provide direct petrographic support for primitive melts matching kimberlite bulk chemistry in the lower SCLM. A majority of kimberlitic olivines show normal (decreasing Mg#) core to rim zonation. Cores of normal-zoned kimberlitic olivines are typically homogeneous, but collectively define a field with a range in Mg # and invariant or slightly decreasing Ni towards more Fe-rich compositions. The most Mg-rich cores of normal-zoned olivines typically have Mg# in the range 94-93, but there are marked differences in the Fe-rich extreme of the normal-zoned population between different kimberlite clusters. Olivine rims typically define a field characterized by steeply decreasing Ni, coupled with invariant or slightly increasing or decreasing Mg#, which invariably overlaps the Fe-extreme of core compositions of the relatively Mg-rich, normal-zoned olivines. Consequently, while there is a sharp inflection in chemical gradient between the respective fields of cores and rims, they nevertheless define a continuous compositional field. Trace element modelling demonstrates that these zonation patterns can be explained in terms of a Raleigh crystallization model. Most, if not all kimberlites are characterized by a subordinate group of olivine macrocrysts with cores that are Fe-rich relative to the field for rims, and thus show reverse zonation, which are interpreted to be linked to the Cr-poor megacryst suite. Rare Mg-rich olivines (relative to rims), have high-pressure inclusions of garnet, clinopyroxene and orthopyroxene. When present, such inclusions often show disequilibrium features such as internal chemical zonation. This points to a very short mantle residence time prior to entrainment by the host kimberlite, indicating a link to the Cr-rich megacryst suite rather than mantle peridotites. In addition to a variable, but generally subordinate proportion of olivines derived from Cr-poor and Cr-rich megacrysts, xenocrysts derived from disaggregated mantle peridotites will undoubtedly be present. While their proportions are difficult to quantify, the collective evidence points to a cognate origin for a majority of kimberlitic olivines. A kimberlite magma ascent model is proposed which provides a framework for understanding both olivine compositional variation and apparently enigmatic internal and external olivine morphology.
Earth and Planetary Science Letters, Vol. 572, 1, 117118
Africa, South Africa
deposit - Premier, Roberts Victor, Jagersfontein
Abstract: Multiple sulphur isotopic compositions of sulphides from Kaapvaal craton mantle eclogites allow to elucidate the recycling of sulphur into the deep Earth and to differentiate between recycled crust and mantle origins of eclogite-hosted sulphides, including the precious metals that they capture. We present multiple sulphur isotope ratio measurements by secondary ion mass spectrometry for sulphides from a collection of mantle-derived eclogite xenoliths from Proterozoic and Mesozoic kimberlite occurrences in South Africa (Premier, Roberts Victor, Jagersfontein). Previous work established that the host eclogites have elemental and oxygen isotopic compositions in support of seawater-altered oceanic lithosphere protoliths, and for many of these xenolith suites Archean ages have been suggested. The eclogite-hosted sulphides have values from ?5.7 to ‰, with the upper end of this wide range representing the highest-ever recorded composition of material derived from the Earth's mantle. The values range from ?0.29 to ‰ and do not record significant mass-independent sulphur isotope fractionation, i.e., there is no compelling S-MIF signature. Most of the sulphide grains have values that fall within a range between ?6 and ‰, and they probably retain an isotopic record of sulphides that formed originally within altered oceanic crust. In contrast, the highly positive values from +13 to ‰ detected in sulphide grains from a single eclogite xenolith are similar to those of marine sulphates, which were probably a minor sulphur component of the oceanic crustal protolith. The lack of a significant S-MIF signature in the eclogitic sulphides that show evidence for a recycled crust origin implies that this sulphur component stems from a post-Archean surficial reservoir. This finding suggests that the cratonic mantle eclogites may have formed from post-Archean oceanic crust (e.g., Paleoproterozoic eclogite protoliths), or - as is preferred here - the ‘surficial’ sulphur was introduced into the cratonic root during relatively young metasomatic events and is thus unrelated to eclogite petrogenesis and Archean continent formation.
Geochemistry, Geophysics, Geosystems, 10.1029/2021GC009691 55p. Pdf
Africa, South Africa, Lesotho, Europe, Greenland
craton
Abstract: Understanding the rate at which temperature changes with increasing depth (geothermal gradients) within ancient continental crust and its underlying mantle (cratonic lithosphere) is essential for understanding the internal structure of Earth. However, understanding geothermal gradients requires a chemical and physical understanding of deep cratonic lithosphere (up to ?200 km depth) and samples from such depths are only available as fragments hosted in melts that originate there (e.g., kimberlites). This limited sample availability of the cratonic mantle roots has resulted in some properties of this domain, used in geothermal modeling, to be poorly constrained. Here we use samples of cratonic mantle lithosphere to determine one critical and poorly constrained parameter used in modeling geothermal gradients—the heat produced from the radiogenic decay of K, U, and Th to their daughter isotopes. We measure these elements in the samples via in situ laser ablation methods to quantify their potential heat production. Comparing our results to previous estimates of heat production, our new estimates produce differences in the thicknesses of cratonic lithosphere calculated from modeled geothermal gradients by >10 km depending on the chosen lithological model. The results from this study provide an important new data set for constraining heat production in cratonic mantle peridotites.
Journal of Geochemical Exploration, Vol. 23, 13p. Pdf
Africa, South Africa
geophysics - magnetics
Abstract: In this study, the southern margin of the Archean Kaapvaal Craton in South Africa is selected to investigate the occurrences of potential kimberlite bodies. Ground magnetic survey was conducted to identify potential targets for further exploration. Euler 3D deconvolution and Keating correlation coefficients are the processing techniques that were applied to the ground magnetic data to identify geological features that correspond to kimberlite models. These techniques revealed several potential targets that resemble geologic models of kimberlite bodies. Seven of these targets (Targets A, B, C, D, E, F and G), spatially cluster along or at the intersections of linear structures, which is consistent with one of the primary geological conditions that control the emplacement of kimberlite bodies. A follow-up soil sampling and analysis was conducted to assess the geochemistry of soils at the seven targets. The major element geochemistry of soil samples suggest that Target B possesses residual soils that originated from kimberlite intrusion, while the remaining six samples show geochemical characteristics of soils derived from crustal rocks. The composition of compatible (Ni, Cr, V, Co, Cu and Zn) and incompatible (Nb, Zr, Sr, Ce, and Ba) trace elements of Target B shows similarity with the known Group 1 Kimberlites locally and globally, thus confirming that Target B most probably belongs to Group 1 Kimberlite petrological clan. This, however, does not preclude the possibility of modification of kimberlite chemistry by crustal assimilation during ascent and post-emplacement processes such as weathering as demonstrated by elevated concentrations of SiO2, Al2O3 and Rb and low content of MgO. In light of this, Target B may be interpreted as a potentially contaminated and weathered Group 1 Kimberlite pipe which intruded the Karoo Supergroup at the intersection of linear structures. This finding is consistent with the presence of large number of known diamondiferous kimberlites in this region, which post-date the formation of the Karoo Supergroup.
Abstract: The cratonic lithosphere-asthenosphere boundary is commonly invoked as the site of sheared peridotite and megacryst formation, a well-recognized petrological assemblage whose genetic relationships—if any—remain poorly understood. We have undertaken a comprehensive petrology and Sr-Nd-Hf-Ca isotope study of sheared peridotite xenoliths and clinopyroxene megacrysts from the c. 1150 Ma Premier kimberlite pipe on the central Kaapvaal craton in South Africa. New textural and mineral trace element evidence suggests that strong tectonic and magmatic overprinting affected the lower cratonic mantle over a vertical distance of ?50 km from the lithosphere-asthenosphere boundary located at ?200-225 km depth. Although modification of the central Kaapvaal cratonic mantle is commonly linked to the c. 2056 Ma Bushveld large igneous event, our thermobarometry, mantle redox, and Sr-Nd-Hf-Ca isotope data support a model in which volatile-rich low-volume melts and associated high-density fluids refertilized the lithosphere base shortly before or during asthenosphere-derived kimberlite and carbonatite magmatism at around 1150 Ma. This episode of lithospheric mantle enrichment was facilitated by exceptionally strong shear movements, as are recorded in the plastically deformed peridotites. We argue that stress-driven segregation of percolating carbonated melts contributed to megacryst formation along, or in close proximity to, shear zones within the cratonic mantle lithosphere. Integration of our results from the Kaapvaal craton and modern petrological concepts allows for the identification of a lithosphere-asthenosphere transition zone between ?150 and 225 km depth. This horizon is defined by intersections of the ?40-42 mW m-2 Premier paleogeotherm with (1) CO2-H2O-present solidus curves for peridotite (upper bound), and (2) typical mantle adiabats with potential temperatures between 1315 and 1420 °C (lower bound). At Premier, the most strongly deformed sheared peridotites occur mainly between ?160 and 185 km depth, firmly within the lithosphere-asthenosphere transition zone. Contrary to many previous models, we suggest that sheared peridotite formation occurs in localized deformation zones spaced out across the entire width of the lithosphere-asthenosphere transition zone, rather than being restricted to a single thin layer at the craton base where mantle flow causes viscous drag. Hence, plate-tectonic stresses acting on the lower cratonic lithosphere may be accommodated by extensive networks of shear zones, which provide transient pathways and sinks for percolating volatile-rich melts, linking the formation of megacrysts and sheared peridotites.
Abstract: The cratonic lithosphere-asthenosphere boundary is commonly invoked as the site of sheared peridotite and megacryst formation, a well-recognized petrological assemblage whose genetic relationships—if any—remain poorly understood. We have undertaken a comprehensive petrology and Sr-Nd-Hf-Ca isotope study of sheared peridotite xenoliths and clinopyroxene megacrysts from the c. 1150 Ma Premier kimberlite pipe on the central Kaapvaal craton in South Africa. New textural and mineral trace element evidence suggests that strong tectonic and magmatic overprinting affected the lower cratonic mantle over a vertical distance of ?50 km from the lithosphere-asthenosphere boundary located at ?200-225 km depth. Although modification of the central Kaapvaal cratonic mantle is commonly linked to the c. 2056 Ma Bushveld large igneous event, our thermobarometry, mantle redox, and Sr-Nd-Hf-Ca isotope data support a model in which volatile-rich low-volume melts and associated high-density fluids refertilized the lithosphere base shortly before or during asthenosphere-derived kimberlite and carbonatite magmatism at around 1150 Ma. This episode of lithospheric mantle enrichment was facilitated by exceptionally strong shear movements, as are recorded in the plastically deformed peridotites. We argue that stress-driven segregation of percolating carbonated melts contributed to megacryst formation along, or in close proximity to, shear zones within the cratonic mantle lithosphere. Integration of our results from the Kaapvaal craton and modern petrological concepts allows for the identification of a lithosphere-asthenosphere transition zone between ?150 and 225 km depth. This horizon is defined by intersections of the ?40-42 mW m-2 Premier paleogeotherm with (1) CO2-H2O-present solidus curves for peridotite (upper bound), and (2) typical mantle adiabats with potential temperatures between 1315 and 1420 °C (lower bound). At Premier, the most strongly deformed sheared peridotites occur mainly between ?160 and 185 km depth, firmly within the lithosphere-asthenosphere transition zone. Contrary to many previous models, we suggest that sheared peridotite formation occurs in localized deformation zones spaced out across the entire width of the lithosphere-asthenosphere transition zone, rather than being restricted to a single thin layer at the craton base where mantle flow causes viscous drag. Hence, plate-tectonic stresses acting on the lower cratonic lithosphere may be accommodated by extensive networks of shear zones, which provide transient pathways and sinks for percolating volatile-rich melts, linking the formation of megacrysts and sheared peridotites.
Journal of African Earth Sciences, Vol. 185, 104414, 19p. Pdf
Africa, South Africa
carbonatite
Abstract: The Salpeterkop volcano is spatially part of the Sutherland Suite of alkaline rocks in the Northern Cape. It is one of the best preserved volcanoes in South Africa with part of the tuff ring still intact, remnants of the ejecta mantle outside the crater still preserved, and is host to epiclastic rocks, including ash and lapillistone and water lain sediments, inside the crater. New dates from apatites and phlogopites from Salpeterkop suggest an age close to 70 Ma. This Upper Cretaceous age is supported by the silicified wood found within the epiclastic sediments. Its relationship to the alkaline rocks in this cluster is not entirely clear but field evidence suggests that initial olivine melilitites and ultramafic bodies were followed by the main eruption that produced Salpeterkop. Clear igneous components in the associated breccias and pyroclastics are rare but indicate that this volcano was linked to an alkaline (trachytic) intrusion driven by phreatic magmatism. This is further highlighted by the presence of (nepheline?) syenite xenoliths in some carbonatite breccias and dykes that are part of the later carbonatites with its associated hydrothermal alteration products. Although the carbonatites are largely late-stage, there is evidence of earlier carbonatite activity from a precursor carbonatite dyke that has off-set an olivine melilitite dyke. Relatively unaltered pyroclastics, associated with two vents, northeast and northwest of the crater respectively, represent the final phase of this volcanic centre. Finally, the preservation of the Salpeterkop crater and its associated volcaniclastics highlights the change of intense landscape denudation, that ensued from Gondwana break-up to the end of the Cretaceous, to a period of drastically reduced erosion rates during the Cenozoic Era.
Journal of Petrology, doi.org/petrology/egab090 65p. Pdf
Africa, South Africa
deposit - Roberts Victor
Abstract: The origin of the eclogites that reside in cratonic mantle roots has long been debated. In the classic Roberts Victor kimberlite locality in South Africa, the strongly contrasting textural and geochemical features of two types of eclogites have led to different genetic models. We studied a new suite of 63 eclogite xenoliths from the former Roberts Victor Mine. In addition to major- and trace-element compositions for all new samples, we determined 18O/16O for garnet from 34 eclogites. Based on geochemical and textural characteristics we identify a large suite of Type I eclogites (n = 53) consistent with previous interpretations that these rocks originate from metamorphosed basaltic-picritic lavas or gabbroic cumulates from oceanic crust, crystallised from melts of depleted MORB mantle. We identify a smaller set of Type II eclogites (n = 10) based on geochemical and textural similarity to eclogites in published literature. We infer their range to very low ?18O values combined with their varied, often very low Zr/Hf ratios and LREE-depleted nature to indicate a protolith origin via low-pressure clinopyroxene-bearing oceanic cumulates formed from melts that were more depleted in incompatible elements than N-MORB. These compositions are indicative of derivation from a residual mantle source that experienced preferential extraction of incompatible elements and fractionation of Zr-Hf during previous melting.
Abstract: Kaapvaal lamproites, also known as orangeites, are H2O-rich, diamondiferous, highly micaceous, ultrapotassic rocks. Olivines in kimberlites have been shown to be extremely useful in tracking melt evolution, highlighting the importance of the chemical effects of SCLM assimilation on asthenosphere-derived melts. Kaapvaal lamproites are derived from melting metasomatised SCLM and may be expected to form an endmember to the asthenosphere melt-SCLM trend defined by kimberlites. In this contribution, we use olivine composition in Kaapvaal lamproites to further understand melt evolution in the SCLM and assess the similarity between Kaapvaal lamproite, other diamondiferous lamproites, and kimberlite petrogenesis in cratonic regions. We present olivine composition for representative on- and off-craton Kaapvaal lamproites from Finsch and Melton Wold, respectively. Olivines from these Kaapvaal lamproites are characterized by distinct core and rim zones, regardless of the size of individual grains. Polycrystalline grains are abundant at Finsch but relatively rare at Melton Wold. The olivine cores from both occurrences are predominantly Mg-rich (Fo>89) whereas Fe-rich cores (Fo<89) are rare. Mg-rich cores are interpreted to be derived from the disaggregation of mantle peridotites, including sheared peridotites, whereas Fe-rich cores are derived from olivines of the Cr-poor megacryst suite. The average Fo and NiO concentrations of the Melton Wold cores are lower than Finsch cores, likely related to less refractory off-craton mantle. The olivine rims at Finsch and Melton Wold are characterized by reverse zoning with ranges of Fo89-92 and Fo90-91, respectively. The rims are interpreted to represent crystallisation related to a complex interplay between increasing oxidation, assimilation of orthopyroxene, and increasing alkali content of the melt during evolution. The average core and rim compositions of Finsch and Melton Wold, in conjunction with data from diamondiferous lamproites of other cratonic regions, define a broad positive correlation. Kaapvaal lamproites have Mg-rich core and rim compositions, similar to that of Lac de Gras kimberlites, and interpreted to reflect sampling and equilibration of low volume Kaapvaal lamproite melt with refractory mantle. In contrast to Lac de Gras kimberlites, Kaapvaal lamproites have high abundances of groundmass phlogopite that reflect metasomatic material in the SCLM source, likely present as veins within refractory peridotite. This suggests that increasing proportions of melt-metasomatised SCLM interactions are not always linked with increasing Fe content of melts. We show that the petrogenesis of Kaapvaal lamproites is similar to that of kimberlites and lamproites from other cratonic regions, however, the high abundance of phlogopite and Fo-rich olivine rims suggest a distinct metasomatic lithology in the source and that olivine composition; i.e., a proxy for melt composition, may be strongly controlled by melt volume during melt-SCLM interactions.
Africa, South Africa, Europe, Greenland, China, Russia, Siberia, Canada, South America, Brazil
subduction, metasomatism
Abstract: To investigate halogen heterogeneity in the subcontinental lithospheric mantle (SCLM), we measured the concentrations of Cl, Br, and I in kimberlites and their mantle xenoliths from South Africa, Greenland, China, Siberia, Canada, and Brazil. The samples can be classified into two groups based on halogen ratios: a high-I/Br group (South Africa, Greenland, Brazil, and Canada) and a low-I/Br group (China and Siberia). The halogen compositions were examined with the indices of crustal contamination using Sr and Nd isotopes and incompatible trace elements. The results indicate that the difference between the two groups was not due to different degrees of crustal contamination but from the contributions of different mantle sources. The low-I/Br group has a similar halogen composition to seawater-influenced materials such as fluids in altered oceanic basalts and eclogites and fluids associated with halite precipitation from seawater. We conclude that the halogens of the high-I/Br group are most likely derived from a SCLM source metasomatized by a fluid derived from subducted serpentinite, whereas those of the low-I/Br group are derived from a SCLM source metasomatized by a fluid derived from seawater-altered oceanic crust. The SCLM beneath Siberia and China could be an important reservoir of subducted, seawater-derived halogens, while such role of SCLM beneath South Africa, Greenland, Canada, and Brazil seems limited.
Contribution to Mineralogy and Petrology, Vol. 1777, 2, 10.1007/s00410-021-01880-8
Africa, South Africa
deposit - Lace
Abstract: We studied diamond inclusions in the 133 Ma Lace kimberlite of the Kroonstad Group II kimberlite cluster (Kaapvaal craton) to compare them to diamonds beneath the adjacent coeval Voorspoed kimberlite. The studied 288 Lace diamonds are mostly colorless dodecahedral Type IaAB. Based on diamond inclusions (DI), 38 Lace diamonds were classified as eclogitic (44%, 19 samples), peridotitic (35%, 15 samples), and websteritic (9%, 4 samples). The diamonds formed from mantle carbon (?13C?=?? 9.1 to ? 2.5 ‰ for 18 samples), with the exception of one eclogitic diamond (?13C?=?? 19.2 ‰). A rare zircon inclusion provides age constraints for the Lace eclogite protolith at 3.2?±?0.4 Ga (Lu-Hf model age) and Lace eclogite diamond formation at 188?±?37 Ma (U-Pb age). The eclogite protolith age suggests its formation contemporaneous with the lower crustal magmatism and metamorphism in the Central Kaapvaal craton, complementary to the tonalite-trondhjemite-granodiorite magmatism in the region and synchronous with the consolidation of the Eastern Kaapvaal Block. Two distinct kinds of eclogites are found to host Lace diamonds, (1) Fe-rich eclogites located at 160-190 km, and (2) more calcic-magnesian eclogites with mineral compositions identical to websteritic DIs, that derive from shallower lithospheric depths. Various thermobarometric methods applied to Lace diamonds and DIs constrain the Lace geotherm as reflecting a surface heat flow below or equal to 38 mW/m2 and a lithosphere thickness of at least 220 km, at the time of kimberlite eruption. These thermal parameters demonstrate an excellent match between the thermal state of the Voorspoed and Lace mantle segments that persisted from the Archean to Cretaceous times. The Lace peridotitic-to-eclogitic diamond ratio (5/4) does not differ much from the Voorspoed DI ratio (6/4), but a hot and spatially restricted carbonatitic metasomatism event affected the Voorspoed peridotitic mantle to create the majority of Voorspoed diamonds. The contrast in the mineralogy of DIs in Lace and Voorspoed diamonds highlights the very local (ca. 10 km) extent of the metasomatism and heating, as well as the variability of the diamond-forming processes at the same spatial scale.
Geological Society of London Special Publication 513, pp. 17-44.
Africa, South Africa
lamproites
Abstract: Orangeites are a significant source of diamonds, yet ambiguity surrounds their status among groups of mantle-derived potassic rocks. This study reports mineralogical and geochemical data for a c. 140 Ma orangeite dyke swarm that intersects the Bushveld Complex on the Kaapvaal craton in South Africa. The dykes comprise distinctive petrographic varieties that are linked principally by olivine fractionation, with the most evolved members containing minor amounts of primary carbonate, sanidine and andradite garnet in the groundmass. Although abundant groundmass phlogopite and clinopyroxene have compositions that are similar to those of cratonic lamproites, these phases show notable Ti-depletion, which we consider a hallmark feature of type orangeites from the Kaapvaal craton. Ti-depletion is also characteristic of bulk rock compositions and is associated with strongly depleted Th-U-Nb-Ta contents at high Cs-Rb-Ba-K concentrations. The resultant high large ion lithophile element/high field strength element ratios of orangeites suggest that mantle source enrichment occurred by metasomatic processes in the proximity of ancient subduction zones. The Bushveld-intersecting orangeite dykes have strongly enriched Sr-Nd-Hf isotopic compositions (initial 87Sr/86Sr = 0.70701-0.70741; ?Nd = ?10.6 to ?5.8; ?Hf = ?14.4 to ?2.5), similar to those of other orangeites from across South Africa. Combined with the strong Ti-Nb-Ta depletion, this ubiquitous isotopic feature points to the involvement of ancient metasomatized mantle lithosphere in the origin of Kaapvaal craton orangeites, where K-rich metasomes imparted a ‘fossil’ subduction geochemical signature. Previous geochronology studies identified ancient K-enrichment events within the Kaapvaal cratonic mantle lithosphere, possibly associated with collisional tectonics during the 1.2-1.1 Ga Namaqua-Natal orogeny of the Rodinia supercontinent cycle. It therefore seems permissible that the cratonic mantle root was preconditioned for ultrapotassic magma production by tectonomagmatic events that occurred along convergent plate margins during the Proterozoic. However, reactivation of the K-rich metasomes had to await establishment of an extensional tectonic regime, such as that during the Mesozoic breakup of Gondwana, which was accompanied by widespread (1000 × 750 km) small-volume orangeite volcanism between 200 and 110 Ma. Although similarities exist between orangeites and lamproites, these and other potassic rocks are sufficiently distinct in their compositions such that different magma formation processes must be considered. In addition to new investigations of the geodynamic triggers of K-rich ultramafic magmatism, future research should more stringently evaluate the relative roles of redox effects and volatile components such as H2O-CO2-F in the petrogeneses of these potentially diamondiferous alkaline rocks.
Abstract: We report Zn-isotope compositions of garnet, clinopyroxene, and whole rocks for 14 Type I and 10 Type II eclogites from the Roberts Victor kimberlite (Kaapvaal Craton, South Africa) that were previously analyzed for Mg-O isotopes. Type II eclogites are the protoliths of the highly metasomatized Type I. Garnet and clinopyroxene in Type II eclogites have ?66Zn from 0.14‰ to 0.50‰ and from 0.29‰ to 0.58‰, respectively; reconstructed whole-rock ?66Zn is from 0.24‰ to 0.54‰, which is higher than typical mantle values (0.16-0.20‰). Their heavy Zn- and light Mg- and O-isotope compositions (?26Mg = -1.1‰ to -0.14‰, ?18O = 2.3‰ to 4.9‰) cannot originate from subducted, carbonate-rich, altered oceanic crust, which is enriched in heavy Zn-O and light Mg isotopes. The low ?18O may be inherited from parental melts derived from low-?18O mantle sources like those that produced the Weltevreden komatiites of the Kaapvaal Craton. The high ?66Zn and low ?26Mg reflect diffusion-driven Zn-Mg-isotope exchange between peridotites and the parental melts during their emplacement in the deep lithosphere. Type I eclogites have reconstructed whole-rock ?66Zn from 0.03‰ to 0.43‰ and garnet ?18O from 6‰ to 9.1‰ but show more scatter in inter-mineral Zn-isotope fractionation than Type II, reflecting incomplete equilibration during later metasomatism by carbonatitic-to-kimberlitic melts. Our evidence from multiple isotopes thus suggests that the Roberts Victor eclogites might have crystallized from deep-seated melts at mantle depths.
Abstract: The thermochemical structure of the subcontinental mantle holds information on its origin and evolution that can inform energy and mineral exploration strategies, natural hazard mitigation and evolutionary models of Earth. However, imaging the fine-scale thermochemical structure of continental lithosphere remains a major challenge. Here we combine multiple land and satellite datasets via thermodynamically constrained inversions to obtain a high-resolution thermochemical model of central and southern Africa. Results reveal diverse structures and compositions for cratons, indicating distinct evolutions and responses to geodynamic processes. While much of the Kaapvaal lithosphere retained its cratonic features, the western Angolan-Kasai Shield and the Rehoboth Block have lost their cratonic keels. The lithosphere of the Congo Craton has been affected by metasomatism, increasing its density and inducing its conspicuous low-topography, geoid and magnetic anomalies. Our results reconcile mantle structure with the causes and location of volcanism within and around the Tanzanian Craton, whereas the absence of volcanism towards the north is due to local asthenospheric downwellings, not to a previously proposed lithospheric root connecting with the Congo Craton. Our study offers improved integration of mantle structure, magmatism and the evolution and destruction of cratonic lithosphere, and lays the groundwork for future lithospheric evolutionary models and exploration frameworks for Earth and other terrestrial planets.
Abstract: We report Zn-isotope compositions of garnet, clinopyroxene, and whole rocks for 14 Type I and 10 Type II eclogites from the Roberts Victor kimberlite (Kaapvaal Craton, South Africa) that were previously analyzed for Mg-O isotopes. Type II eclogites are the protoliths of the highly metasomatized Type I. Garnet and clinopyroxene in Type II eclogites have ?66Zn from 0.14‰ to 0.50‰ and from 0.29‰ to 0.58‰, respectively; reconstructed whole-rock ?66Zn is from 0.24‰ to 0.54‰, which is higher than typical mantle values (0.16-0.20‰). Their heavy Zn- and light Mg- and O-isotope compositions (?26Mg = ?1.1‰ to ?0.14‰, ?18O = 2.3‰ to 4.9‰) cannot originate from subducted, carbonate-rich, altered oceanic crust, which is enriched in heavy Zn-O and light Mg isotopes. The low ?18O may be inherited from parental melts derived from low-?18O mantle sources like those that produced the Weltevreden komatiites of the Kaapvaal Craton. The high ?66Zn and low ?26Mg reflect diffusion-driven Zn-Mg-isotope exchange between peridotites and the parental melts during their emplacement in the deep lithosphere. Type I eclogites have reconstructed whole-rock ?66Zn from 0.03‰ to 0.43‰ and garnet ?18O from 6‰ to 9.1‰ but show more scatter in inter-mineral Zn-isotope fractionation than Type II, reflecting incomplete equilibration during later metasomatism by carbonatitic-to-kimberlitic melts. Our evidence from multiple isotopes thus suggests that the Roberts Victor eclogites might have crystallized from deep-seated melts at mantle depths.
Journal of Geophysical Research, 10.1029/2021JB023105, 28p.
Africa, South Africa
geophysics - magnetotellurics
Abstract: The present-day composition of Earth's tectonic plates results from past geological processes. We can learn about Earth's composition from deep rock samples that are carried to the surface during volcanic eruptions and by probing its physical properties, like electrical conductivity, with geophysics. In southern Africa, there are extensive deep rock samples, which have been brought to the surface by kimberlite volcanoes that also host diamonds, and also extensive geophysical data. In this article, we compare the rock compositions with electrical conductivity to learn more about Earth's composition. Our results show that the oldest parts of the plates, which retain compositions similar to their initial composition, appear resistive. On the other hand, regions that have been intruded by deep fluids or molten rock can be resistive or conductive, depending on the types of minerals that were formed during the intrusion. The kimberlite volcanoes mostly erupted through the edges of the most resistive parts of the plates and did not erupt through the conductors. These results will help us to make more accurate interpretations about the composition of parts of the Earth where we do not have deep rock samples.
