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The Sheahan Diamond Literature Reference Compilation - Technical Articles based on Major Region - Quebec
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]
Montregian Hills I. Petrography, Major and Trace Element Chemistry, and Strontium Isotopic Chemistry of the Western Intrusions, Mounts Royal, St. Bruno and Johnson.
Fahrig, W.F., Christie, K.W., Chown, E.H., Janes, D., Machado, N.
The tectonic significance of some basic dyke swarms in the Canadian Superior province with special reference to The geochemistry and paleomagnetism of th
Canadian Journal of Earth Sciences, Vol. 23, No. 2, February pp. 238-253
The tectonic significance of some basic dike swarms in the Canadian Superior Province with special reference to geochemistry and paleomagnetism of Mistassini swarm
Canadian Journal of Earth Sciences, Vol. 23, pp. 238-53.
Trace element charactertistics of the Strange Lake Zirconium, Yttrium, Niobium,and Berylium rare earth elements (REE) mineralization and the host peralkaline granite
Geological Association of Canada (GAC) Annual Meeting, Vol. 11, p. 102. (abstract.)
Quebec, Labrador
Rare earth, Zirconium, Berylium, REE, yttrium, Carbonatite, Alkaline rock
A comparison of the mineralogy of Point of Rocks Mesa, New Mexico with that of Mont. St. Hilaire Quebec and Ilimaussaq Greenland and the Kolapeninsula, USS
New Mexico Geology, Vol. 8, No. 2, May p. 42. extened abstract
Comparative amphibole chemistry of the Montregian and White Mountain alkaline suites and the origin of amphibole megacrysts in alkali basalts andlamprophyres
Mineralogical Magazine, Vol. 52, No. 364, No. 1, March pp. 91-104
Petrology and pyroxene chemistry of Montregian dykes-the origin of concentric zoning and green cores in clinopyroxenes from alkali basalts andlamprophyres
Canadian Journal of Earth Sciences, Vol. 25, No. 12, December pp. 2041-2058
A reappraisal of the geology and geochemistry of the Zr-Y-Nb-Be and rare earth elements (REE)mineralized Strange Lake peralkalinepluton, Quebec-Labrador
Geological Association of Canada (GAC)/Mineralogical Association of Canada (MAC) Vancouver 90 Program with Abstracts, Held May 16-18, Vol. 15, p. A12. Abstract
The role of hydrothermal processes in the granite hosted Zirconium, Yttrium, rare earth elements (REE) deposit at Strange Lake, Quebec/Labrador: evidence from fluid inclusions
Geochimica et Cosmochimica Acta, Vol. 54, pp. 2403-2418
Kimzeyite (Zr-garnet) from alnoites at Ile Bizard and Oka Quebec:mineralogy and petrogenesis
Geological Association of Canada (GAC)/Mineralogical Association of Canada (MAC) Vancouver 90 Program with Abstracts, Held May 16-18, Vol. 15, p. A135. Abstract
The role of hydrothermal processes in the granite-hosted Zirconium, Yttrium, rare earth elements (REE) deposit at Strange Lake Quebec, Labrador- evidence from fluid inclusions-comment
Geochimica et Cosmochimica Acta, Vol. 55, No. 11, pp. 3443-3447
Decompressiong reactions and P=T conditions in high grade rocks, northernLabrador; P-T paths individual samples and implications for early Prot. tectonicevol
Journal of Petrology, Vol. 32, No. 1, February pp. 139-168
Metamorphosed boninitic basalts, arc tholeiites, and cryptic volcanics tratigraphy from the Elzevir Terrane of the Grenville Province, Calumet mine, Quebec
Canadian Journal of Earth Sciences, Vol. 29, No. 1, January pp. 26-34
uranium-lead (U-Pb) geochronology of deformation and metamorphism across a central transect of the Early Proterozoic: Tornget Orogen, North River map area, Labrador.
Canadian Journal of Earth Sciences, Vol. 30, pp. 1470-89.
Toft, P.B., Scowen, A.H., Arkani-Hamed, J., Francis, D.
Demagnetization by hydration in deep crustal rocks in the Grenville Province of Quebec, Canada: implications for magnetic anomalies of continental collision zones
Mineraux lourdes dans le till et ex pour le diamant, region du Lac Vernon (34J) terroire du Nouveau Quebec. M.I. Project de cartographie du Grand Nord.
Quebec Ministere des Resources Naturelles, (FRE), MB2002-01.
Geochemistry of boninite type volcanic rocks in the Frotet Evans greenstone belt, Opawica subprovince Quebec: implications for the evolution of Archean belts
Precambrian Research, Vol. 115, No.1-4, pp. 349-71.
Ruee vers le diamant au Quebec - Otish, Wemindji, Alluviaq, Torngat, Temiscamingue, Desmaraisville, la Beaver, Renard, Nottaway, Caniapiscau, Bienville, Aigneault
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
Paleomagnetism, U Pb geochronology and geochemistry of Lac Esprit and other dyke swarms, James Bay area, Quebec: implications for Paleoproterozoic deformation
Canadian Journal of Earth Sciences, Vol. 44, 5, pp. 643-664.
Indicator mineralogy of kimberlite boulders and sand samples from the Lac Baby and Sharp Lake eskers, Lake Timiskaming field, western Quebec and northeast Ontario
Geological Survey of Canada Open File, No. 5050, 21p.
The lithospheric root beneath Hudson Bay, Canada from Rayleigh wave dispersion: no clear seismological distinction between Archean and Proterozoic mantle.
Rogermitchellite, a new mineral species from Mont Hilaire Quebec: description, structure, determination and relationship with HFSE bearing cyclosilicates.
The origin of Triassic/Jurassic kimberlite magmatism, Canada: two mantle sources revealed from the Sr-Nd isotopic composition of groundmass perovskite.
Hunt, L., Stachel, T., Grutter, H., Armstrong, J., McCandless, T.E., Simonetti, A., Tappe, S.
Small mantle fragments from the Renard kimberlites, Quebec: powerful recorders of mantle lithosphere formation and modification beneath the eastern Superior Craton.
Roulleau, E., Pinti, D.L., Stevenson, R.K., Takahata, N., Sano, Y., Pitre, F.
N, Ar and Pb isotopic co-variation in magmatic minerals: discriminating fractionation processes from magmatic sources in Montregian Hills, Quebec, Canada.
In situ determination of major and trace elements in calcite and apatite, and U-Pb ages of apatite from the Oka carbonatite complex: insights into a complex crystallization history.
Economic geology of Renard 3, Quebec, Canada: a diamondiferous, multi-phase pipe infilled with hypabyssal and tuffisitic kimberlite.
Proceedings of the 10th. International Kimberlite Conference, Vol. 2, Special Issue of the Journal of the Geological Society of India,, Vol. 2, pp. 241-256.
Geological Society of London Special Publication: Continent formation through time., No. 389, pp. 41-67.
Canada, Ontario, Quebec
Geotectonics
Abstract: Hudson Bay Lithospheric Experiment (HuBLE) was designed to understand the processes that formed Laurentia and the Hudson Bay basin within it. Receiver function analysis shows that Archaean terranes display structurally simple, uniform thickness, felsic crust. Beneath the Palaeoproterozoic Trans-Hudson Orogen (THO), thicker, more complex crust is interpreted as evidence for a secular evolution in crustal formation from non-plate-tectonic in the Palaeoarchaean to fully developed plate tectonics by the Palaeoproterozoic. Corroborating this hypothesis, anisotropy studies reveal 1.8 Ga plate-scale THO-age fabrics. Seismic tomography shows that the Proterozoic mantle has lower wavespeeds than surrounding Archaean blocks; the Laurentian keel thus formed partly in post-Archaean times. A mantle transition zone study indicates ‘normal’ temperatures beneath the Laurentian keel, so any cold mantle down-welling associated with the regional free-air gravity anomaly is probably confined to the upper mantle. Focal mechanisms from earthquakes indicate that present-day crustal stresses are influenced by glacial rebound and pre-existing faults. Ambient-noise tomography reveals a low-velocity anomaly, coincident with a previously inferred zone of crustal stretching, eliminating eclogitization of lower crustal rocks as a basin formation mechanism. Hudson Bay is an ephemeral feature, caused principally by incomplete glacial rebound. Plate stretching is the primary mechanism responsible for the formation of the basin itself.
Abstract: Mantle-derived carbonatites are igneous rocks dominated by carbonate minerals. Intrusive carbonatites typically contain calcite and, less commonly, dolomite and siderite as the only carbonate minerals. In contrast, lavas erupted by the only active carbonatite volcano on Earth, Oldoinyo Lengai, Tanzania, are enriched in Na-rich carbonate phenocrysts (nyerereite and gregoryite) and Na-K halides in the groundmass. The apparent paradox between the compositions of intrusive and extrusive carbonatites has not been satisfactorily resolved. This study records the fortuitous preservation of halite in the intrusive dolomitic carbonatite of the St.-Honoré carbonatite complex (Québec, Canada), more than 490 m below the present surface. Halite occurs intergrown with, and included in, magmatic minerals typical of intrusive carbonatites; i.e., dolomite, calcite, apatite, rare earth element fluorocarbonates, pyrochlore, fluorite, and phlogopite. Halite is also a major daughter phase of melt inclusions hosted in early magmatic minerals, apatite and pyrochlore. The carbon isotope composition of dolomite (?13C = –5.2‰) and Sr-Nd isotope compositions of individual minerals (87Sr/86Sri = 0.70287 in apatite, to 0.70443 in halite; ?Nd = +3.2 to +4.0) indicate a mantle origin for the St.-Honoré carbonatite parental melt. More radiogenic Sr compositions of dolomite and dolomite-hosted halite and heavy oxygen isotope composition of dolomite (?18O = +23‰) suggest their formation at some time after magma emplacement by recrystallization of original magmatic components in the presence of ambient fluids. Our observations indicate that water-soluble chloride minerals, common in the modern natrocarbonatite lavas, can be significant but ephemeral components of intrusive carbonatite complexes. We therefore infer that the parental magmas that produce primary carbonatite melts might be enriched in Na and Cl. This conclusion affects existing models for mantle source compositions, melting scenarios, temperature, rheological properties, and crystallization path of carbonatite melts.
Geochimica et Cosmochimica Acta, in press available 20p.
Canada, Ontario, Quebec
Ungava craton
Abstract: Although terrestrial picritic magmas with FeOTOT ?13 wt.% are rare in the geological record, they were relatively common ca. 2.7 Ga during the Neoarchean episode of enhanced global growth of continental crust. Recent evidence that ferropicritic underplating played an important role in the ca. 2.74–2.70 Ga reworking of the Ungava craton provides the impetus for a comparison of ca. 2.7 Ga ferropicrite occurrences in the global Neoarchean magmatic record. In addition to the Fe-rich plutons of the Ungava craton, volumetrically minor ferropicritic flows, pyroclastic deposits, and intrusive rocks form parts of the Neoarchean greenstone belt stratigraphy of the Abitibi, Wawa, Wabigoon and Vermillion domains of the southern and western Superior Province. Neoarchean ferropicritic rocks also occur on five other Archean cratons: West Churchill, Slave, Yilgarn, Kaapvaal, and Karelia; suggesting that ca. 2.7 Ga Fe-rich magmatism was globally widespread. Neoarchean ferropicrites form two distinct groups in terms of their trace element geochemistry. Alkaline ferropicrites have fractionated REE profiles and show no systematic HFSE anomalies, broadly resembling the trace element character of modern-day ocean island basalt (OIB) magmas. Magmas parental to ca. 2.7 Ga alkaline ferropicrites also had high Nb/YPM (>2), low Al2O3/TiO2 (<8) and Sc/Fe (-3 × 10?4) ratios, and were enriched in Ni relative to primary pyrolite mantle-derived melts. The high Ni contents of the alkaline ferropicrites coupled with the low Sc/Fe ratios are consistent with derivation from olivine-free garnet-pyroxenite sources. The second ferropicrite group is characterized by decisively non-alkaline primary trace element profiles that range from flat to LREE-depleted, resembling Archean tholeiitic basalts and komatiites. In contrast to the alkaline ferropicrites, the magmas parental to the subalkaline ferropicrites had flat HREE, lower Nb/YPM (<2), higher Al2O3/TiO2 (8-25) and Sc/Fe (-4 × 10?4) ratios, and were depleted in Ni relative to melts of pyrolitic peridotite; suggesting they were derived from garnet-free peridotite sources. Neodymium isotopic evidence indicates that the source of alkaline ferropicrites was metasomatically enriched shortly before magma generation (-3.0 Ga), but the subalkaline ferropicrites do not show evidence of precursor metasomatism. The metasomatic enrichment of the alkaline ferropicrite sources may have been accompanied by conversion of Fe-rich peridotite to secondary garnet-pyroxenite. Melting experiments on "pyrolitic" compositions and consideration of the dependence of the density of silicate liquids on pressure and temperature, suggest that ferropicrites cannot originate by melting of normal terrestrial mantle (Mg-number = 0.88-0.92) at high pressures and temperatures. The geochemical similarity between the subalkaline ferropicrites and the shergottite-nakhlite-chassigny (SNC) and howardite-eucrite-diogenite (HED) differentiated meteorites suggests, however, that the Fe-rich mantle may originate from the infall of Fe-rich chondritic meteorites. The occurrence of ca. 2.7 Ga Fe-rich rocks on at least six cratons that are commonly coeval with the more ubiquitous komatiites and Mg-tholeiites is consistent with the existence of heterogeneous Fe-rich "plums" throughout the Neoarchean mantle. The paucity of ferropicrites in the post-2.7 Ga geological record suggests that majority of these Fe-rich plums have been melted out during the global Neoarchean melting of the mantle.
Abstract: Magmatic volatiles are critically important in the petrogenesis of igneous rocks but their inherent transience hampers the identification of their role in magmatic and mineralization processes. We present evidence that magmatic volatiles played a critical role in the formation of the 1894 Ma Paleoproterozoic Montviel alkaline-carbonatite complex, Canada, and the related carbonatite-hosted REE-Nb deposit. Field and drill core relationships indicate that lithological units of the complex were emplaced in the following order: clinopyroxenites, melteigites, ijolites, melanosyenites, leucosyenites, granites, lamprophyric silicocarbonatites, rare magnesiocarbonatites, calciocarbonatites, ferrocarbonatites, late mixed carbonatites, kimberlitic silicocarbonatites and polygenic breccias. Magmatic minerals within these units were systematically metasomatized. In undersaturated silicate rocks, augite recrystallized to aegirine–augite and aegirine, plagioclase recrystallized to albite, and nepheline recrystallized with analcime, cancrinite and albite. Primary biotite was replaced by secondary, REE-rich metasomatic biotite, particularly along fractures and alteration pockets. In carbonatites, liquidus phases consisted of calcite and dolomite and were recrystallized to ferroan dolomite, ankerite, siderite, barytocalcite, witherite and strontianite, which are intimately related to the REE-bearing carbonates and fluorocarbonates. Biotite is common to all lithologies, ranges in REE concentrations from 1.5 to 230 ppm and yielded subsolidus crystallization temperatures ranging from 770 °C to 370 °C. Sm-Nd isotope analyses from biotite and aegirine-augite yield a range of ?Nd values (+ 3.4 to ? 3.0) that suggests mixing of fluids from three sources during the crystallization of the Montviel magmas. The clinopyroxenites to melteigite, ijolites and melanosyenites crystallized augite and biotite with initial ?Nd value ? 3.4 and these minerals were metasomatized by a 1st fluid, lowering their ?Nd to values comprised between 0.8 and 3.4. Silicocarbonatites and carbonatites subsequently crystallized aegirine-augite and biotite with initial ?Nd value ? 2.6 and a 2nd fluid metasomatized the minerals to lower ? values. Both the 1st and the 2nd fluids eventually mixed with a 3rd recrystallizing aegirine-augite and biotite and lower their ?Nd values down to ? 3.0. The results presented herein suggest that the mantle magmas evolved through 4 distinct mantle pulses by fractional crystallization, mixing of depleted mantle fluids with crustal fluids, and metasomatism. Some of the silicate rocks also show evidence of assimilation of wall rock as part of their petrogenetic evolution. During the last stages of its evolution in carbonatites, the fluid source transited from the depleted mantle to the crust and we speculate that this resulted in a violent explosive eruption creating the diatreme-shaped, HREE-rich polygenic breccia.
Symposium on critical and strategic materials, British Columbia Geological Survey Paper 2015-3, held Nov. 13-14, pp. 265-
Canada, Quebec
Rare earths
Abstract: Rare earth elements (REE) are strategic metals vital to global economic growth because they are used in a wide range of high-technology industries (e.g., energy, transport, and telecommunications; Walters et al., 2011). The world production and reserves are mainly owned by China. In 2008, the Chinese government introduced export quotas on rare metals, which led to a global search for new sources of REE. Québec has substantial REE resources (Simandl et al., 2012), which may contribute to future production. Gosselin et al. (2003) and Boily and Gosselin (2004) inventoried rare metals (REE, Zr, Nb, Ta, Be, and Li) occurrences and deposits in Québec and, based mainly on lithological association, subdivided them into seven types: 1) deposits associated with peraluminous granitic complexes; 2) deposits associated with carbonatite complexes; 3) deposits associated with peralkaline complexes; 4) deposits associated with placers and paleoplacers; 5) iron oxide, Cu, REE, and U deposits; 6) deposits associated with granitic pegmatites, migmatites, and peraluminous to metaluminous granites; and 7) deposits associated with calc-silicate and metasomatized rocks or skarns. Herein we review REE mineralization in the province, adopting a more genetic scheme based on the classifi cation of Walters et al. (2011). The REE occurrences and deposits are subdivided into primary deposits, formed by magmatic and/ or hydrothermal processes, and secondary deposits, formed by sedimentary processes and leaching. Primary deposits are then subdivided into four types: 1) carbonatite complex-associated; 2) peralkaline igneous rock-associated; 3) REE-bearing Iron- Oxide-Copper-Gold (IOCG) deposits; and 4) hyperaluminous/ metaluminous granitic pegmatite-, granite-, and migmatiteassociated deposits, and skarns. Secondary deposits are subdivided into two deposit types: 1) placers and paleoplacers and 2) REE-bearing ion-adsorption clays.
Symposium on critical and strategic materials, British Columbia Geological Survey Paper 2015-3, held Nov. 13-14, pp. 69-74.
Canada, Quebec
Alkalic
Abstract: The Crevier alkaline intrusion is in the Grenville Province, north of the Lac Saint-Jean region of Québec (Fig. 1). It covers ~25 km2 (Bergeron, 1980) and intrudes charnockitic suites in the allochthon belt defi ned by Rivers et al. (1989). This intrusion has a U-Pb zircon age of 957.5 ± 2.9 Ma (Groulier et al., 2014) and is oriented N320°, along the axis of crustal weakness known as the Waswanipi-Saguenay corridor (Bernier and Moorhead, 2000). This corridor is related to the Saguenay graben, which hosts the Saint-Honoré (Niobec) Nb-Ta-REE deposit and Montviel REE deposit. The age of the Saint-Honoré carbonatite was estimated at 584 to 650 Ma (K-Ar whole rock; Vallée and Dubuc, 1970; Boily and Gosselin, 2004). The Montviel intrusion has a U-Pb zircon age of 1894 ± 3.5 Ma (David et al., 2006; Goutier, 2006). These crystallization ages are very different and cannot be related to a single event for the injection of alkaline intrusions. As mapped by Bergeron (1980), the Crevier alkaline intrusion is broadly composed of syenite and carbonatite rocks (Fig. 2). The Nb- Ta mineralization consists of pyrochlore hosted by a nepheline syenite dike swarm in the centre of the intrusion. The highest REE concentrations, up to 729 ppm La and 1465 ppm Ce, are at the edge of the Crevier alkaline intrusion (Niotaz sud showing; Fig. 2).
Symposium on critical and strategic materials, British Columbia Geological Survey Paper 2015-3, held Nov. 13-14, pp. 75-82.
Canada, Quebec
Niobium
Abstract: The mineralogy of rare earth element (REE) ore deposits is critical in understanding their petrogenesis but also has signifi cant implications for metallurgy. Like many ore deposits, high-grade rocks do not necessarily equate to positive economic viability and this is especially true for REE deposits. Consequently, knowledge of sample mineralogy acquired early in a project’s life can lead to more effi cient exploration programs through confi rmation of either ‘good’ or ‘bad’ mineralogy. Many REE minerals show fi ne grain sizes and their accumulation can be diffi cult to recognize in hand sample or drill core with an unaided eye. Knowledge of their distribution before sampling can ensure that the best rocks or core lengths are sampled for petrographic or detailed study. REE minerals generally have complex yet diagnostic absorption patterns in visible to shortwave infrared (VNIRSWIR) refl ectance spectra that are driven primarily by REErelated 4f-4f intraconfi gurational electronic transitions. Our recent research (Turner et al., 2014, Turner 2015) has focused on three important mineral classes: REE fl uorocarbonates (bastnaesite, synchysite, and parisite), REE phosphates (monazite, xenotime, and britholite), and REE-bearing silicates (cerite, mosandrite, kainosite, zircon and eudialyte). Refl ectance spectra were acquired in the visible to short wave infrared regions (500 nm to 2500 nm) and samples were characterized using scanning electron microscopy and electron microprobe analysis. The results of our work and publications from other research groups (e.g., Rowan et al., 1986, Swayze et al., 2013, Hoefen et al., 2014, Boesche et al., 2015) have shown the strong applicability of refl ectance spectroscopy and hyperspectral imaging to understanding, exploring, and exploiting rare earth element ore deposits and their associated rocks.
A 2169 Ma U-Pb baddeleyite age for the Otish gabbro, Quebec: implications for correlation of Proterozoic magmatic events and sedimentary seuences in the eastern Superior province.
Canadian Journal of Earth Sciences, Vol. 53, 2, pp. 119-128.
Abstract: For decades, geologists have debated the geodynamic processes that operated in the young Earth. In the Archean, 4 and 2.5 billion years ago, the interior of the planet was much hotter which led to more rapid convection and, according to some authors, to an absence of plate tectonics. Komatiites (Fig. 1) - volcanic rocks with abnormal, olivine-enriched compositions - are thought to result from high-degrees of partial melting of extremely hot parts of the Earth’s mantle. This interpretation is blurred, however, by uncertainty as to the water content of komatiitic magmas. There are two schools of thought on this question: the first proposes that the magmas were dry (<0.1% water) and very hot (> 1600°C), and were produced in mantle plumes from the base of the mantle; the second suggests that the magmas were hydrated, with lower melting temperatures, and had formed in subduction settings. The analysed komatiite melt contained 30% magnesium oxide and 0.6% water and began to crystallize at a relatively low temperature of 1530°C. The chemical composition of the magma and low oxygen fugacity are inconsistent with a subduction setting. he mantle plume (orange) traverses the transition zone, which contains excess H2O, F and Cl in ringwoodite and/or wadsleyite (high pressure polymorphs of olivine).The plume is hot enough to be partially molten near the top of the transition zone (small black dots) and entrains hydrous melt (blue shapes) either from the layer at the upper boundary of the transition zone or from the hot boundary between the plume and the transition zone. Alternatively or additionally, the plume may entrain solid wadsleyite from the transition zone (green shapes). All these hydrous materials introduce H2O and possibly F and Cl into the plume and accelerate its melting (larger black dots). Further ascent of the plume generates more melt during decompression (large black dots), which then separates from the source and ascends to the surface without reaction with peridotite (purple stripes). Instead, the authors suggest that the magmas were generated in a deep mantle plume and that the water and other volatile components, especially the halogens (F, Cl), were entrained into the komatiitic magma as it passed through the transition zone between the upper and lower mantle, at a depth below 410 km (Fig. 3). This implies the existence of a deep reservoir of water in the mantle: a portion of the mantle containing a few thausends of parts per million of water in high pressure polymorphs of olivine wadsleyite, ringwoodite. This water may have accumulated during the primordial accretion of the Earth or by the unexpectedly early subduction of hydrated slabs that became trapped in the transition zone. Finally, the authors propose that modern mantle plumes do not extract water from the transition zone because they are colder and therefore entirely solid when they crossed the transition zone.
The 4th Colloquium on Diamonds - source to use held Gabarone March 1-3, 2010, 14p.
Canada, Quebec
Deposit - Renard
Abstract: The Renard kimberlite cluster is located in the Monts Otish region of Quebec, Canada. A Canadian National Instrument (NI) 43-101 compliant resource statement for the Renard kimberlites 2, 3, 4 and 9 and the Lynx kimberlite dyke was first issued in 2008 followed by a Preliminary Economic Assessment and the development of a conceptual mine plan. Following a successful drill program in 2009 tbat greatly expanded the amount of kimberlite in Renard 2, a revised resource statement was issued in December 2009 comprising 23 mitlion carats of Indicated Mineral Resources and 13 million carats of Inferred Mineral Resources, a threefold increase on the previous estimate. The project is currently the focus of a second Preliminary Economic Assessment and it is expected that a full feasibility and permitting program will commence in 2010 leading to the creation of Quebec's first diamond mine by 2013
Abstract: Neoproterozoic kimberlite, ultramafic lamprophyre, and carbonatite magmatic activity was widespread across the Canadian-Greenland Shield. Models to explain the preponderance of this deeply-derived CO2-rich magmatism between 680-540 Ma range from impingement of multiple mantle plumes to rifting activity linked to the breakout of the Laurentian plate from the Rodinia supercontinent configuration. We add to the debate about the origin of kimberlite magmas and evaluate possible mantle sources of the 655 Ma ‘diamond-rich’ Renard (new SIMS U/Pb perovskite ages) and 629 Ma ‘barren’ Wemindji kimberlites on the eastern Superior craton in Quebec, Canada. Our Sr-Nd-Hf and carbon isotope data (87Sr/86Sri = 0.70241-0.70442; ?Ndi = + 0.2 to + 4.8; ?Hfi = + 0.3 to + 6.5; ?13C = ? 5.6 to ? 3.9‰) suggest a common and moderately depleted convecting upper mantle source region for both the Renard and Wemindji kimberlites, which occur 400-km apart in the interior of the Superior craton. In contrast, the low Os isotope ratios (187Os/188Osi = 0.11078-0.12620; ?Osi = ? 13.7 to ? 1.6) and unfractionated chondritic relative HSE abundances (Os, Ir, Ru, Pt, Pd, Re) indicate significant involvement of ancient refractory cratonic mantle material in kimberlite magma formation. Our model calculations suggest that for both the diamond-rich Renard and the barren Wemindji kimberlite magmas up to 30% of the Os was derived from refractory cratonic peridotites. This material might have been assimilated by originally more CO2-rich carbonated silicate melts derived from the asthenosphere. We also show that the geochemical and Sr-Nd-Hf-Os isotopic compositions of the Renard and Wemindji kimberlites do not require significant input from melts derived from olivine-poor cratonic mantle lithologies such as MARID-type veins and pyroxenites/eclogites. This contrasts with the petrogenesis of deeply-derived volatile-rich potassic magmas found along the peripheries of cratons (e.g., ultramafic lamprophyres, kamafugites, and olivine lamproites), a setting where abundant non-peridotitic components have been added to the lithospheric mantle over the course of continent evolution. Provided that CO2-rich melts, such as proto-kimberlites, occur near the solidus of volatile-fluxed peridotites, no excess mantle heat is required in their formation. This important but often overlooked constraint, together with the observation that there exist no spatial or temporal relationships between the Superior craton kimberlites and Large Igneous Provinces during the Late Neoproterozoic, suggests that kimberlite magmatic activity was tectonically controlled. In our preferred model, ubiquitous CO2-rich proto-kimberlite melts form during volatile-controlled redox melting processes at ambient mantle temperatures in a thermal boundary layer directly beneath thick cratonic lithosphere. The success rate of ‘evolving’ hybrid kimberlite magmas reaching Earth’s surface increases when tensile stresses propagate into the > 200 km thick keels of continental lithosphere. These conditions are frequently met during fast and changing plate motions associated with the assembly and breakup of supercontinents.
Abstract: Neoproterozoic kimberlite, ultramafic lamprophyre, and carbonatite magmatic activity was widespread across the Canadian-Greenland Shield. Models to explain the preponderance of this deeply-derived CO2-rich magmatism between 680-540 Ma range from impingement of multiple mantle plumes to rifting activity linked to the breakout of the Laurentian plate from the Rodinia supercontinent configuration. We add to the debate about the origin of kimberlite magmas and evaluate possible mantle sources of the 655 Ma ‘diamond-rich’ Renard (new SIMS U/Pb perovskite ages) and 629 Ma ‘barren’ Wemindji kimberlites on the eastern Superior craton in Quebec, Canada. Our Sr-Nd-Hf and carbon isotope data (87Sr/86Sri = 0.70241-0.70442; ?Ndi = + 0.2 to + 4.8; ?Hfi = + 0.3 to + 6.5; ?13C = ? 5.6 to ? 3.9‰) suggest a common and moderately depleted convecting upper mantle source region for both the Renard and Wemindji kimberlites, which occur 400 km apart in the interior of the Superior craton. In contrast, the low Os isotope ratios (187Os/188Osi = 0.11078-0.12620; ?Osi = ? 13.7 to ? 1.6) and unfractionated chondritic relative HSE abundances (Os, Ir, Ru, Pt, Pd, Re) indicate significant involvement of ancient refractory cratonic mantle material in kimberlite magma formation. Our model calculations suggest that for both the diamond-rich Renard and the barren Wemindji kimberlite magmas up to 30% of the Os was derived from refractory cratonic peridotites. This material might have been assimilated by originally more CO2-rich carbonated silicate melts derived from the asthenosphere. We also show that the geochemical and Sr-Nd-Hf-Os isotopic compositions of the Renard and Wemindji kimberlites do not require significant input from melts derived from olivine-poor cratonic mantle lithologies such as MARID-type veins and pyroxenites/eclogites. This contrasts with the petrogenesis of deeply-derived volatile-rich potassic magmas found along the peripheries of cratons (e.g., ultramafic lamprophyres, kamafugites, and olivine lamproites), a setting where abundant non-peridotitic components have been added to the lithospheric mantle over the course of continent evolution. Provided that CO2-rich melts, such as proto-kimberlites, occur near the solidus of volatile-fluxed peridotites, no excess mantle heat is required in their formation. This important but often overlooked constraint, together with the observation that there exist no spatial or temporal relationships between the Superior craton kimberlites and Large Igneous Provinces during the Late Neoproterozoic, suggests that kimberlite magmatic activity was tectonically controlled. In our preferred model, ubiquitous CO2-rich proto-kimberlite melts form during volatile-controlled redox melting processes at ambient mantle temperatures in a thermal boundary layer directly beneath thick cratonic lithosphere. The success rate of ‘evolving’ hybrid kimberlite magmas reaching Earth’s surface increases when tensile stresses propagate into the > 200 km thick keels of continental lithosphere. These conditions are frequently met during fast and changing plate motions associated with the assembly and breakup of supercontinents.
Abstract: A prominent dike of camptonite cuts the Middle Ordovician Tétreauville Formation of the Trenton Group in the Montréal-Est quarry operated by Lafarge Canada Inc. The “Lafarge” dike is strikingly porphyritic, with largely anhedral macrocrysts of unzoned calcic amphibole up to 13 cm across. The macrocrysts are rimmed with ferri-kaersutite resembling the amphibole in the fine-grained matrix of the camptonite. The magnesio-hastingstite macrocrysts have virtually the same composition as the matrix; they thus grew without much of a boundary layer. The magma crystallized in a disequilibrium way as a pseudo-unary system. The macrocrysts are unusually enriched in Fe3+ (approximately 44% of the total iron), yet locally enclose globules of immiscible sulfide melt. The magma became oxygenated owing to preferential loss of hydrogen upon the dissociation of aqueous gas bubbles. The amygdaloidal macrocrysts have a relatively high ?D value because of this loss of H2; the values of ?18O are typical of an upper mantle source. Camptonite dikes are very common on Mont Royal. Like the Lafarge dike, they likely arose by the disequilibrium crystallization of batches of the parental melt of asthenospheric origin.
Abstract: The Ashram Zone, which is host to the Ashram Rare Earth Element (REE) Deposit, occurs within the Eldor Carbonatite Complex, Québec, Canada. The complex is located within the Paleoproterozoic New Québec Orogen (Labrador Trough), and has been subjected to greenschist metamorphism and folding during the Hudsonian Orogeny at 1.75 Ga. To date, consanguineous undersaturated alkaline rocks have not been recognized within or adjacent to the complex. It is evident that the bulk compositions of the rocks, essentially magnesiocarbonatites and ferrocarbonatites, do not represent those of liquid compositions, as many are complex breccias which have been subjected to later hydrothermal activity. The Ashram Zone is dominated by diverse textural varieties of carbonatite which include: fluorite-rich schlieren carbonatites; coarse-to-medium grained granular carbonatites; fine grained, commonly mosaic-textured, quartz-bearing carbonatites; and colloform carbonatites. Compositional and textural data are provided for the minerals present in the carbonatites. The major rock-forming minerals are diverse Ca-Mg-Fe carbonates, fluorite, and quartz. The carbonates range in their compositional evolution from rare dolomite through ferrodolomite and magnesian siderite to siderite. The principal REE-bearing minerals of the Ashram Deposit are monazite-(Ce) and monazite-(Nd), with lesser amounts of bastnaesite-(Ce) and bastnaesite-(Nd). The minor and accessory mineral suite is characterized by the presence of apatite, phlogopite, xenotime, diverse Sc- and sn-bearing Nb-Ti-minerals (niobian rutile, nioboaeschynite, samarskite), barite, sphalerite, several uncommon, but here relatively abundant, Ba- and Ba-Be minerals (bafertisite, magbasite, barylite, betrandite, sanbornite, cebaite), yangzhumingite, cassiterite, galena, pyrite, and rare magnetite and potassium feldspar. Pyrochlore is absent and the Nb-Ti oxide assemblage is similar to that found in NYF-pegmatites associated with F-rich, A-type granitoids. The mineralogy of the Ashram Deposit, compared to that of other carbonatites associated with undersaturated silicate rocks is unique, especially with respect to the abundance of fluorite and monazite (commonly with Nd-enrichment), Ba-Be-enrichment, the NYF-type Nb-Ti oxide assemblage (especially xenotime, Y-Nb-aeschynite, samarskite), phlogopite-potassium feldspar quartz-rich residua with granitoid characteristics, paucity of magnetite, pyrochlore, and Sr-bearing carbonates. The Ashram Deposit is considered to be a late-magmatic-to-hydrothermal F-REE magnesio-to-ferrocarbonatite derived from as yet unknown consanguineous antecedents.
Abstract: Near Meech Lake, Québec, the edges of Mesoproterozoic carbonatite dikes are composed of calcite, dolomite, fluorapatite, phlogopite, amphibole, and pyrochlore. The carbonatite is separated from amphibole-fenite by a narrow, fine-grained reaction selvage of phlogopite pierced with long prisms of amphibole. The amphibole is mainly richterite, but it extends to magnesio-arfvedsonite (overgrowth, crystal rim). Uranium-rich pyrochlore is metamict and ranges from calciopyrochlore to kenopyrochlore with Ta-U enrichment in crystal rims. Chemical characteristics of the suite are: (1) F and Nb highest in the selvage, and (2) decline of Sr and Ce outwards from the carbonatite. A similar pattern (this research) is found at Fen, Norway. Rare earths are enriched in LREE with smooth downward-sloping patterns, in chondrite-normalized curves, to HREE. Two major surges of mineralization are suggested: (1) early, metasomatic-alkalic, creating fenites with enrichment in Mg, Na, and K; and (2) later igneous depositing carbonatites and introducing first F, P, and Nb, then Ca, Sr, and Ce. Thermochemical and geochronological data place carbonate equilibration at 700 °C and the emplacement at 1026 Ma b.p. Calciocarbonatites, in monzonitic orthogneiss, are enriched in Ba and Ce. They are composed of baryte, calcite, phlogopite, fluorapatite, magnesio-riebeckite, and non-metamict allanite-(Ce). A mica selvage is present, but amphibole fenite is almost completely lacking. Magnesiocarbonatite has a well-developed selvage against granite but lacks significant amphibole fenite. In breccia cement at nearby Fortune Lake, pyrochlore is associated with abundant fluorapatite but lacks carbonates. The Cambro-Proterozoic calciocarbonatite near Fen, Norway is particularly Nb-rich in breccia zones, and pyroxene fenite takes the place of amphibole fenite at Meech Lake. In contrast to a relatively anorogenic regime during carbonatite petrogenesis at Fen, metamorphism has obscured pyrochlore zonation and enhanced amphibole growth at Meech Lake
Abstract: The Renard 65 pipe is located in the Otish Mountains, Quebec, Canada. It is one of nine diamondiferous kimberlite pipes in the ~ 640 Ma Renard cluster and is the largest of four pipes in the Renard Mine reserve. Detailed characterizations of the petrographic and compositional features of these pipe-infilling kimberlite rock types supports their classification into three geological units: Kimb65a, Kimb65b, and Kimb65d. These pipe-infilling kimberlites are interpreted to represent the solidified products of two separate magmatic events: Phase A containing Kimb65a, and Phase B containing Kimb65b and Kimb65d. This research demonstrates that the interclast matrix modal mineralogy (diopside + phlogopite + serpentine) in pyroclastic rock types in the Renard 65 kimberlites are inconsistent with origins by hydrothermal alteration involving hydrous meteoric fluids. Detailed investigation of the reactions between granitic and gneissic crustal xenolith lithologies and their host kimberlites, suggests that reactions occur at both magmatic and subsolidus temperatures involving significant volumetric proportions of xenoliths. The assimilation of crustal xenoliths, and contamination of the kimberlite magmas primarily by Si, are demonstrated to result in enhanced degassing of magmatic volatiles during emplacement and stabilization of the hybrid groundmass assemblage diopside + phlogopite + serpentine over the non hybrid groundmass assemblage calcite + phlogopite + serpentine. It is thus interpreted that the spatial distribution of transitional to Kimberley-type pyroclastic kimberlite rock types, which are characterized by diopside-rich and calcite-poor matrix assemblages as observed in the Renard 65 pipe and other similar pipes, is a function of crustal xenolith distribution in the magma during emplacement. This model not only accounts for the features of Kimberley-type pyroclastic kimberlite rock types, but also the spatial distribution of these rock types in numerous pipes which is often not consistent with lateral textural gradations as has been previously proposed. These results further indicate that the different mineralogy and textures of Fort-à-la-Corne-type pyroclastic kimberlites with respect to Kimberley-type pyroclastic kimberlites may be a consequence of not only the structural controls imparted by the host rock lithology with implications for emplacement-related processes, but also the absence of contamination of the magma by silicic crustal xenoliths.
Subsolidus compositional modification of kimberlitic spinel in the Renard 65 kimberlite pipe, Quebec, Canada - implications for the use of spinel chemistry in the identification of kimberlite phases.
Punctuated long lived emplacement history of kimberlites from the Renard cluster, Superior Province, Canada indicated by new high precision U-Pb groundmass perovskite dating.
Canada, Northwest Territories, Quebec, United States, Colorado
deposit, A54, Lynx, Kelsey Lake
Abstract: Eighteen diamond samples from the A154 South kimberlite pipe (Diavik Mine), Slave Craton, Northwest Territories (Canada); sixteen diamond samples from the Lynx kimberlite dyke, Superior Craton, Quebec (Canada) and twelve diamond samples from the Kelsey Lake kimberlite pipe, Wyoming Craton, Colorado (USA), were cut through the core-zones, polished, imaged by cathodoluminescence (CL), and analyzed by secondary ion mass spectrometry (SIMS) for carbon isotope composition and nitrogen abundance. Twenty Kelsey Lake diamond plates, including the twelve crystals analyzed by SIMS, were analyzed by Fourier transform infrared spectrometry (FTIR) for nitrogen concentration and aggregation state. Diamond samples from Diavik and Kelsey Lake have average ?13CPDB and nitrogen contents (atomic ppm) similar to those found by earlier studies: averaging between ? 3.9‰ and 486 ppm, and ? 7‰ and 308 ppm, respectively. Samples from the Lynx dyke, investigated for the first time, are substantially different, having ?13C = ?1.2‰ and nitrogen content = 32 ppm (averages). All three localities have examples of significant variations in nitrogen content (> 100 ppm) within single stones. Carbon isotope variation within individual stones is relatively minor (< 2‰). In terms of nitrogen aggregation, samples from the Kelsey Lake kimberlite are dominated by zones of Type IaA, but mixed-type and Type IaB (less common) stones also occur. For the majority of samples, overall intra-diamond zonations of nitrogen abundances and carbon isotope ratios are not in agreement with modeled trends for single-event Rayleigh fractionation of diamond from fluid under nitrogen-compatible conditions at 1100 °C. The involvement of fluids from subducted crustal reservoirs with exceptionally light, and in the case of Lynx samples, exceptionally heavy ?13CPDB values is necessary to explain the observed growth histories of all the samples studied here.
Continuity of kimberley-type pyroclastic kimberlite phases within Renard 2 over 1,000 m depth - insights to the geological and emplacement model, Superior craton, Canada.
Abstract: A growing number of studies have suggested that hydrothermal remobilization is crucial for the formation of carbonatite-hosted rare earth element (REE) deposits [1-3]. The Ashram REE deposit, hosted by the Paleoproterozoic Eldor Carbonatite Complex [4], is an example of a REE deposit formed mainly due to hydrothermal processes in magnesio- and ferro-carbonatite. The REE minerals in the Ashram deposit, monazite-(Ce), bastnäsite-(Ce), xenotime- (Y) and minor aeschynite-(Y), are secondary, and were precipitated from hydrothermal fluids. They occur mainly as disseminations, in breccia matrices and veins, and as vug fillings. Hydrothermal apatite and fluorite are also present in appreciable quantities in REE-mineralized zones. Monazite- (Ce) was the earliest REE mineral to form, and was followed by xenotime-(Y) and bastnäsite-(Ce). The compositions of the main REE minerals vary with location in the deposit, particularly in respect to their Nd2O3 and ThO2 contents. Two generations of monazite-(Ce) have been distinguished on the basis of their Nd content. Early, low-Nd monazite-(Ce) formed by replacing apatite through the substitution of 3REE3+ for 5Ca2+ + F- ; low-Nd apatite is LREE-enriched compared to apatite. In contrast, the later high-Nd generation, which has a chondrite-normalized REE profile almost perfectly parallel to that of the apatite, is interpreted to have formed by dissolving the Ca2+ and F- of the apatite and reconstituting the REE and phosphate as monazite-(Ce): Ca4.94REE0.060(PO4)3F = 0.060REEPO4 + F- + 4.94Ca2+ + 2.94PO4 3- Bastnäsite-(Ce) developed as a replacement of monazite- (Ce) through ligand exchange (F- and CO3 2- for PO4 3- ), while preserving the original REE chemistry. A combination of magmatic zone-refinement and hydrothermal remobilization, involving a chloride-bearing fluid, contributed to the formation of a carbonatite-hosted REE deposit.
Geochemical Perspectives Letters, Vol. 3, pp. 230-237.
Canada, Quebec, Anticosti Island
carbon cycle
Abstract: Chemical weathering of silicate rocks is a primary drawdown mechanism of atmospheric carbon dioxide. The processes that affect weathering are therefore central in controlling global climate. A temperature-controlled “weathering thermostat” has long been proposed in stabilising long-term climate, but without definitive evidence from the geologic record. Here we use lithium isotopes (?7Li) to assess the impact of silicate weathering across a significant climate-cooling period, the end-Ordovician Hirnantian glaciation (~445 Ma). We find a positive ?7Li excursion, suggestive of a silicate weathering decline. Using a coupled lithium-carbon model, we show that initiation of the glaciation was likely caused by declining CO2 degassing, which triggered abrupt global cooling, and much lower weathering rates. This lower CO2 drawdown during the glaciation allowed climatic recovery and deglaciation. Combined, the data and model provide support from the geological record for the operation of the weathering thermostat.
Earth and Planetary Science Letters, Vol. 478, pp. 52-58.
Canada, Quebec
Mistastin crater
Abstract: Bolide impacts influence primordial evolution of planetary bodies because they can cause instantaneous melting and vaporization of both crust and impactors. Temperatures reached by impact-generated silicate melts are unknown because meteorite impacts are ephemeral, and established mineral and rock thermometers have limited temperature ranges. Consequently, impact melt temperatures in global bombardment models of the early Earth and Moon are poorly constrained, and may not accurately predict the survival, stabilization, geochemical evolution and cooling of early crustal materials. Here we show geological evidence for the transformation of zircon to cubic zirconia plus silica in impact melt from the 28 km diameter Mistastin Lake crater, Canada, which requires super-heating in excess of 2370?°C. This new temperature determination is the highest recorded from any crustal rock. Our phase heritage approach extends the thermometry range for impact melts by several hundred degrees, more closely bridging the gap between nature and theory. Profusion of >2370?°C superheated impact melt during high intensity bombardment of Hadean Earth likely facilitated consumption of early-formed crustal rocks and minerals, widespread volatilization of various species, including hydrates, and formation of dry, rigid, refractory crust.
Abstract: Alkaline and carbonatite rocks are relatively rare but offer the opportunity to study the contribution of fluids in the genesis of mantle and crustal rocks because they are commonly affected by metasomatism. Carbonate minerals represent versatile archives of mantle and crustal magmatic-hydrothermal processes because they can have magmatic, metasomatic or hydrothermal origins and because they host the trace elements, stable and radiogenic isotopes required to unravel their petrogenesis. Previous studies have shown that the 1894 Ma Montviel alkaline?carbonatite complex was emplaced through four injections of volatile-saturated, mantle magmas which evolved through fractional crystallization, mixing of mantle and crustal fluids and metasomatism. Trace element analyses and ?18O, ?13C, 87Sr/86Sr and 143Nd/144Nd isotope compositions of metasomatic and hydrothermal carbonates further support that each magma injection was accompanied by a volatile phase. Variations in trace element concentrations suggest that the carbonatite might have exsolved from a metasomatized mantle or hybrid silicate?carbonatite magma, and that the fluid composition evolved towards higher REE and lower HFSE with increasing degree of segregation of the carbonatite magma and the silicate source. A strong correlation between the C-O-Sr isotopic systems show that mantle fluids mixed with crustal fluids, increasing the 87Sr/86Sr from mantle to crustal values, and driving the C and O isotopic ratios towards respectively lighter and heavier values. The Sm/Nd isotopic system was weakly coupled with the other isotopic systems as depleted mantle fluids mixed with crustal fluids and metasomatized the crystallizing magmas, thereby redistributing the REE and affecting their Sm/Nd ratios. The Nd isotopes suggest that the mixed mantle/crustal fluids redistributed the rare earth elements, producing ultra-depleted (?Nd = + 10), normally depleted (?Nd = + 4) and slightly enriched (?Nd = ? 2) isotopic compositions.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0567-y 9p.
Canada, Quebec
deposit - Renard
Abstract: The Renard 2 kimberlite pipe is one of nine diamondiferous kimberlite pipes that form a cluster in the south-eastern portion of the Superior Province, Québec, Canada and is presently being extracted at the Renard Mine. It is interpreted as a diatreme-zone kimberlite consisting of two Kimberley-type pyroclastic units and related country rock breccias, all cross-cut by coherent kimberlite dykes and irregular intrusives. Renard 2 has been the subject of numerous diamond drilling campaigns since its discovery in 2001. The first two geological models modelled kimberlite and country rock breccia units separately. A change in modelling philosophy in 2009, which incorporated the emplacement envelope and history, modelled the entire intrusive event and projected the pipe shape to depth allowing for more targeted deep drilling where kimberlite had not yet been discovered. This targeted 2009 drilling resulted in a?>?400% increase in the volume of the Indicated Resource. Modelling only the kimberlite units resulted in a significant underestimation of the pipe shape. Current open pit and underground mapping of the pipe shape corresponds well to the final 2015 geological model and contact changes observed are within the expected level of confidence for an Indicated Resource. This study demonstrates that a sound understanding of the geological emplacement is key to developing a reliable 3D geological and resource model that can be used for targeted delineation drilling, feasibility studies and during the initial stages of mining.
Abstract: Granites and pegmatites in the Strange Lake pluton underwent extreme enrichment in high field strength elements (HFSE), including the rare earth elements (REE). Much of this enrichment took place in the most altered rocks, and is expressed as secondary minerals, showing that hydrothermal fluids played an important role in HFSE concentration. Vasyukova et al. (2016) reconstructed a P-T-X path for the evolution of these fluids and provided evidence that hydrothermal activity was initiated by exsolution of fluid during crystallisation of border zone pegmatites (at ~450-500?°C and 1.1?kbar). This early fluid comprised a high salinity (25?wt% NaCl) aqueous phase and a CH4?+?H2 gas. During cooling, the gas was gradually oxidised, first to higher hydrocarbons (e.g., C2H6, C3H8), and then to CO2, and the salinity decreased to 4?wt% (~250-300?°C), before increasing to 19?wt%, due to fluid-rock interaction (~150?°C). Here, we present crush-leach fluid inclusion data on the concentrations of the REE and major ligands at different stages of the evolution of the fluid. The chondrite-normalised REE profile of the fluid evolved from light REE (La-Nd)-enriched at high temperature (~400?°C, Stages 1-2a) to middle REE (Sm-Er)-enriched at 360 to 250?°C (Stages 2b-3) and strongly heavy REE (Tm-Lu)-enriched at low temperature (150?°C, Stage 5). These changes in the REE distribution were accompanied by changes in the concentrations of major ligands, i.e., Cl? was the dominant ligand in Stages 1, 2, 4 and 5, whereas HCO3? was dominant in Stage 3. Alteration of arfvedsonite to aegirine and/or hematite contributed strongly to the mobilisation of the REE. This alteration released middle REE (MREE) and heavy REE (HREE), which either partitioned into the fluid or precipitated directly as bastnäsite-(Ce), ferri-allanite-(Ce) or gadolinite-(Y). Replacement of primary fluorbritholite-(Ce), which crystallised from an immiscible fluoride melt and altered to bastnäsite-(Ce), was also important in mobilising the REE (MREE). This paper presents the first report of the distribution of the REE in an evolving hydrothermal fluid. Using this distribution, in conjunction with information on the changing physicochemical conditions, the study identifies the sources of REE enrichment, reconstructs the path of REE concentration, and evaluates the REE mineralising capacity of the fluid. Finally, this information is integrated into a predictive model for REE mobilisation applicable not only to Strange Lake but any REE ore-forming system, in which hydrothermal processes were important.
Abstract: Geochemical characterization including mineralogical measurements and kinetic testing was completed on samples from the Montviel carbonatite deposit, located in Quebec (Canada). Three main lithological units representing both waste and ore grades were sampled from drill core. A rare earth element (REE) concentrate was produced through a combination of gravity and magnetic separation. All samples were characterized using different mineralogical techniques (i.e., quantitative evaluation of minerals by scanning electron microscopy (QEMSCAN), X-ray diffraction (XRD), and scanning electron microscopy with X-ray microanalysis (SEM-EDS)) in order to quantify modal mineralogy, liberation, REE deportment and composition of REE-bearing phases. The REE concentrate was then submitted for kinetic testing (weathering cell) in order to investigate the REE leaching potential. The mineralogical results indicate that: (i) the main REE-bearing minerals in all samples are burbankite, kukharenkoite-Ce, monazite, and apatite; (ii) the samples are dominated by REE-free carbonates (i.e., calcite, ankerite, and siderite); and (iii) LREE is more abundant than HREE. Grades of REE minerals, sulfides and oxides are richer in the concentrate than in the host lithologies. The geochemical test results show that low concentrations of light REE are leached under kinetic testing conditions (8.8-139.6 ?g/L total light REE). These results are explained by a low reactivity of the REE-bearing carbonates in the kinetic testing conditions, low amounts of REE in solids, and by precipitation of secondary REE minerals.
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0614-7 12p.
Canada, Quebec
deposit - Renard
Abstract: The Renard 2 pipe is currently the deepest-drilled and most extensively studied kimberlite body in the Renard cluster, central Québec, Canada, forming the major component of the Mineral Resource of Stornoway Diamond Corporation’s Renard Mine. Renard 2 is infilled with two distinct kimberlite units that exhibit Kimberley-type pyroclastic kimberlite and related textures. Hypabyssal kimberlite also occurs as smaller cross-cutting sheets and irregular intrusions. The units are distinguished by their rock textures, groundmass mineral assemblages, olivine macrocryst size distributions and replacement products, mantle and country rock xenolith contents, whole rock geochemical signatures, bulk densities and diamond grades. These differences are interpreted to reflect different mantle ascent and near-surface emplacement processes and are here demonstrated to be vertically continuous from present surface to over 1000 m depth. The distinctive petrological features together with sharp, steep and cross-cutting internal contact relationships, show that each unit was formed from a separate batch of mantle-derived kimberlite magma, and was completely solidified before subsequent emplacement of the later unit. The mineralogy and textures of the ultra-fine-grained interclast matrix are consistent with those described at numerous Kimberley-type pyroclastic kimberlite localities around the world and are interpreted to reflect rapid primary crystallization during emplacement of separate kimberlite magmatic systems. The units of fractured and brecciated country rock surrounding the main kimberlite pipe contain kimberlite-derived material including carbonate providing evidence of subsurface brecciation. Together these data show that Renard 2 represents the deeper parts of a Kimberley-type pyroclastic kimberlite pipe system and demonstrates that their diagnostic features result from magmatic crystallisation during subsurface volcanic emplacement processes.
Mineralogy and Petrology, doi.org/10.1007/ s00710-018-0633-4 13p.
Canada, Quebec
deposit - Renard
Abstract: Renard 65, a diamondiferous pipe in the Neoproterozoic Renard kimberlite cluster (Québec, Canada), is a steeply-dipping and downward-tapering diatreme comprised of three pipe-filling units: kimb65a, kimb65b, and kimb65d. The pipe is surrounded by a marginal and variably-brecciated country rock aureole and is crosscut by numerous hypabyssal dykes: kimb65c. Extensive petrographic and mineralogical characterization of over 700 m of drill core from four separate drill holes, suggests that Renard 65 is a Group I kimberlite, mineralogically classified as phlogopite kimberlite and serpentine-phlogopite kimberlite. Kimb65a is a massive volcaniclastic kimberlite dominated by lithic clasts, magmaclasts, and discrete olivine macrocrysts, hosted within a fine-grained diopside and serpentine-rich matrix. Kimb65b is massive, macrocrystic, coherent kimberlite with a groundmass assemblage of phlogopite, spinel, perovskite, apatite, calcite, serpentine and rare monticellite. Kimb65c is a massive, macrocrystic, hypabyssal kimberlite with a groundmass assemblage of phlogopite, serpentine, calcite, perovskite, spinel, and apatite. Kimb65d is massive volcaniclastic kimberlite with localized textures that are intermediate between volcaniclastic and coherent, with tightly packed magmaclasts separated by a diopside- and serpentine-rich matrix. Lithic clasts of granite-gneiss in kimb65a are weakly reacted, with partial melting of feldspars and crystallization of richterite and actinolite. Lithic clasts in kimb65b and kimb65d are entirely recrystallized to calcite + serpentine/chlorite + pectolite and display inner coronas of diopside-aegirine and an outer corona of phlogopite. Compositions are reported for all minerals in the groundmass of coherent kimberlites, magmaclasts, interclast matrices, and reacted lithic clasts. The Renard 65 rocks are texturally classified as Kimberley-type pyroclastic kimberlites and display transitional textures. The kimberlite units are interpreted to have formed in three melt batches based on their distinct spinel chemistry: kimb65a, kimb65b and kimb65d. We note a strong correlation between the modal abundances of lithic clasts and the textures of the kimberlites, where increasing modal abundances of granite/gneiss are observed in kimberlites with increasingly fragmental textures.
Mineralogy and Petrology, doi.org/101007/ s00710-018-0629-0 13p.
Canada, Quebec
deposit - Renard
Abstract: Kimberlites are rare volatile-rich ultramafic magmas thought to erupt in short periods of time (<1 Myr) but there is a growing body of evidence that the emplacement history of a kimberlite can be significantly more protracted. In this study we report a detailed geochronology investigation of a single kimberlite pipe from the Renard cluster in north-central Québec. Ten new high precision ID-TIMS (isotope dilution - thermal ionization mass spectrometry) U-Pb groundmass perovskite dates from the main pipe-infilling kimberlites and several small hypabyssal kimberlites from the Renard 2 pipe indicate kimberlite magmatism lasted at least ~20 Myr. Two samples of the main pipe-infilling kimberlites yield identical weighted mean 206Pb/238U perovskite dates with a composite date of 643.8?±?1.0 Myr, interpreted to be the best estimate for main pipe emplacement. In contrast, six hypabyssal kimberlite samples yielded a range of weighted mean 206Pb/238U perovskite dates between ~652-632 Myr. Multiple dates determined from these early-, syn- and late-stage small hypabyssal kimberlites in the Renard 2 pipe demonstrate this rock type (commonly used to date kimberlites) help to constrain the duration of kimberlite intrusion history within a pipe but do not necessarily reliably record the emplacement age of the main diatreme in the Renard cluster. Our results provide the first robust geochronological data on a single kimberlite that confirms the field relationships initially observed by Wagner (1914) and Clement (1982); the presence of antecedent (diatreme precursor) intrusions, contemporaneous (syn-diatreme) intrusions, and consequent (post-diatreme) cross-cutting intrusions. The results of this detailed U-Pb geochronology study indicate a single kimberlite pipe can record millions of years of magmatism, much longer than previously thought from the classical viewpoint of a rapid and short-duration emplacement history.
Abstract: Magmatism of the Povungnituk Group of the Cape Smith Belt, northern Superior craton, was formed in three stages: (i)early alkaline magmatism and associated carbonatites (undated), (ii) a main flood basalt sequence (Beauparlant Formation) (constrained between 2040 and 1991?Ma), and (iii) a late stage alkaline pulse (Cecilia Formation) (ca. 1959?Ma). We suggest that the main stage of magmatic activity (middle pulse) was of short duration. A new UPb baddeleyite age of 1998?±?6?Ma is obtained from a dolerite sill intruding the uppermost section of the Beauparlant Formation. This age has regional significance because it matches the previously obtained 1998?±?2?Ma age for the Watts Group (Purtuniq) ophiolite of the northern Cape Smith Belt and the 1998?±?2?Ma?U-Pb age of the Minto dykes intruding the craton to the south. These coeval units, along with additional units correlated on paleomagnetic grounds (Eskimo Formation), are interpreted to define a large igneous province (LIP), extending over an area of >400,000?km2, which we herein define as the Minto-Povungnituk LIP. Geochemical comparison between the Watts Group ophiolite, Minto dykes and the mafic Povungnituk Group shows significant differences allowing these data to be divided into two groups and domains within the LIP. A northern domain, comprising the Povungnituk and Watts groups, shows mixing between a depleted mantle source and a more enriched mantle plume-sourced melt. A southern domain comprising the Minto dykes and the paleomagnetically linked Eskimo Formation shows signs of an even more enriched source, while these magmas also show the effect of crustal contamination. Two distinct source mechanisms can be responsible for the observed geochemical differences between the two domains. First, a difference in lithospheric sources, where melting of different portions of Superior craton lithosphere caused the different melt signatures in the interior of the craton. In this case magmatism in the two domains is only related by having the same heat source (e.g.,a mantle plume) interpreted to be located on the northwestern side of the northern Superior craton. Second, two distinct deep mantle sources that remained separated within the ascending plume. This is analogous to some current hotspots interpreted to sample both large low shear velocity provinces (LLSVP) and adjacent ambient deep mantle. This latter interpretation would allow for the use of bilateral chemistry in LIPs as a potential tool for the recognition and mapping of the LLSVP boundaries throughout Earth's history.
Abstract: Large peralkaline complexes are ‘factories’ that have produced a variety of ‘exotic’ minerals including high field strength element minerals. In most cases, these minerals are secondary and crystallise in a hydrothermal paragenesis that is extremely difficult to decipher due to the complexity of the textural relationships. The Strange Lake pluton is one of these complexes, and contains 37 exotic minerals, most of which are secondary. Adding to the difficulty in establishing a comprehensive paragenesis for these minerals and an alteration/precipitation path for the pluton is the fact that there were several stages of crystallisation of the same exotic and common secondary minerals, e.g., bastnäsite, fluocerite, gadolinite, aegirine, fluorite, and zircon. In this paper, we present a model, which describes a detailed path for the alteration and precipitation of minerals in the closed hydrothermal system of a peralkaline granitic pegmatite, based on direct measurements of the evolving composition of the aqueous fluid that exsolved from the late-stage magma crystallising rare-metal pegmatites in the Strange Lake pluton. The driving force for this evolution was cooling-induced oxidation that ultimately transformed the CH4-H2 gas in this fluid to CO2. This led to a large drop in the pH, which was a major control on the composition of the fluid and the crystallisation of secondary minerals. Although large numbers of minerals formed and were replaced during the different stages of fluid evolution, the changing chemistry of the fluid was largely a response to the alteration of four minerals, namely arfvedsonite, elpidite, narsarsukite and fluorite. The earliest stage of alteration, which took place at ~360?°C, was marked by the replacement of arfvedsonite by aegirine. This alteration decreased salinity and released K, Li, and Rb to the fluid, causing K-metasomatism. At ~300?°C, CH4 and higher hydrocarbons reacted to produce CO2. This caused a massive drop in pH from a value?>?10 to a value of ~3 and intense alteration, which included the dissolution of fluorite, the breakdown of elpidite to zircon and quartz and the replacement of narsarsukite by titanite. With ongoing dissolution of fluorite, Ca activity reached a level sufficient to promote the alteration of elpidite to armstrongite or gittinsite. This was accompanied by alteration of arfvedsonite to ferroceladonite and microcline to Al-phyllosilicates, enriching the fluid in Na, Fe and F. Soon after, there was a near total loss of CO2 (at ~230?°C). This loss was catastrophic and was focused along conical fractures (these developed as a result of the collapse of the roof of the pluton), with resultant fragmentation of the rocks along the fluid path. Alteration to phyllosilicates continued after the loss of CO2, as the system cooled to ~190?°C. This marked the beginning of the final stage of alteration, which involved the replacement of arfvedsonite by aegirine and hematite. It also coincided with large scale hematisation within the pluton. Finally, it led to the cementation of the fragments along the fluid path to form the fluorite-hematite ring breccia that is now evident at the margins of the pluton. The model of fluid evolution presented here is potentially applicable to many other peralkaline complexes. The only requirements are that the system was closed until a relatively late stage and that the exsolved fluid was saline and contained a reduced carbonic component. This is a feature of many peralkaline complexes, most notably, the Khibiny and Lovozero complexes in Russia, and Ilímaussaq in Greenland.
Abstract: The Saint-Honoré alkaline complex located near the Saguenay River (Grenville Province, Québec) has a syenite outer rim and concentric units of calcio-, magnesio- to ferro-carbonatite moving towards the centre. The Mg-carbonatite hosts a niobium deposit, and the Fe-carbonatite hosts a rare earth-rich zone at its centre. The Nb mineralization has a close spatial relationship to the syenite enclaves suggesting that the syenites may have played a critical role in concentrating the pyrochlore (Pcl). There are two forms of Nb mineralization: high- and low-grade. Low-grade mineralization is characterized by highly variable Pcl chemistry with higher U concentrations and a low abundance of fluoroapatite (Ap), whereas high-grade mineralization has a consistent Pcl chemistry (low-U), abundant Ap (with many acicular crystals) and more abundant phlogopite and magnetite. Some of the Pcl crystals have been altered to columbite by hydrothermal processes. It is interpreted that the metamict Pcl (rich in radioactive elements) was altered more readily than the Pcl having undamaged crystal structure. The high-grade mineralization is generally located near the syenite enclaves. Syenite enclaves (from a centimetre scale to several tens of metres in size) reacted with the carbonatite magma to produce a phlogopite rim. Ap is also abundant along the immediate contact between the enclaves and Mg-carbonatite. Large enclaves show hydro-fracturing by the carbonatite suggesting they were crystalline enough to be brittle. There are smaller textures (3-6 mm in diameter) that share many similarities with the syenite enclaves; however, these textures are rounded and could be interpreted as being related to liquid immiscibility. The interaction of carbonatite magma with syenite enclaves is interpreted to have started with abundant crystallization of acicular Ap which depleted the magma in F and lowered the magma's Nb-solubility. Pcl then crystallized in abundance in the vicinity of the syenite enclaves to create the economic Nb-rich zone.
Abstract: The Saguenay City alkali province (~ 580 Ma) comprises the Saint-Honoré alkaline complex (carbonatite-syenite), lesser-known minor subsurface carbonatite intrusions and several sets of lamprophyre (sl) dykes. Flat-lying, north-dipping dykes (l-100 cm) that crop out close the Saguenay River/Fjord were formed by multiple intrusions of a very fluid magma. The dykes are continuously variable in composition from carbonatite to ultramafic lamprophyre. Olivine phenocrysts (l-3 mm) are pseudomorphed by serpentine but phlogopite phenocrysts (l-5 mm) are well preserved in a matrix of a fine-grained serpentine, chlorite and carbonate. A few dykes are phoscorites, with abundant phenocrysts of phlogopite, oxides, apatite and accessory baddeleyite. In all dykes, the matrix may have been originally fine-grained or even glassy, and subsequently altered by water dissolved in the original magma. Several dykes contain abundant xenoliths: mostly crustal and possibly one of mantle origin. Low-carbonate dykes have a narrow range in Sr isotopes (0.7030-0.7033) versus the wider range of high-carbonate dykes (0.7032-0.7046), but this distinction is not seen in ?Nd (3.4-4.9). Overall, it appears that each batch of magma was small and came from independent mantle sources. Recently, we found a new set of vertical, NW-directed lamprophyres around the Baie des Ha! Ha!, about 15 km south of the main swarm. They have phlogopite phenocrysts to 50 mm and olivine pseudomorphs. Their contrasting orientation suggests that they have a different age to the Saguenay River dykes, but they have yet to be dated. The overall pattern is of an extensive mantle source that delivered small volumes of volatile-rich ultramafic magmas over a long period. We consider that some of these magma batches accumulated and differentiated in a magma chamber beneath the Saint-Honoré alkaline complex, whereas others rose uninterrupted to high levels of the crust where they were emplaced as dykes.
Abstract: We propose to study the Kipawa peralkaline complex, a rare-earth deposit principally composed of eudialyte, mosandrite and britholite. The Kipawa complex is situated in the Parautochton zone of the Grenville Province in the Tesmiscamingue region of Quebec, 55 km south of contact with Superior Province. The complex consists of peralkaline syenites, amphibolites, gneisses that are intercalated with calc-silicate rocks and marble, and overlain by a peralkaline gneissic granite. The Kipawa complex differs geochemically and petrologically from other well-known peralkaline complexes such as the Illimausaq, Lovozero, Thor Lake or Strange Lake complexes. Classic peralkaline complexes are large, circular igneous complexes, with or without volcanism and have an isotopic signature reflecting mantle origin with different degrees of assimilation and crustal contamination (for example Illimausaq is reported with ?Nd values of 0.4 and -5.7). The Kipawa Complex is a thin, folded stack of sheet imbricates between Kikwissi Suite rocks, McKillop Lake sequence and Red Pine Chute gneiss, suggesting a regional tectonic control. Isotopic analyses carried out by other teamsindicate a strong crustal signature (?Nd = -8.7). Several hypotheses are possible: crustal contamination, hydrothermal activity, fluids alteration during formation, metamorphism or dominant crustal origin. Our objective is to characterize the geochemical and isotopic composition of the Kipawa complex in order to improve our understanding of the age and formation of the complex. Analyses of both whole rocks, eudialytes and zircons will be made to obtain isotopic signatures and determine formation ages and/or post-formation processes.
Abstract: We sampled the mid-Ediacaran Saint-Honoré alkali intrusion and related dykes in the Saguenay City region of Québec for paleomagnetic and U-Pb, 40Ar/39Ar geochonologic study. 40Ar/39Ar geochronology of phlogopite separates from carbonatite of the central intrusion return plateau ages with a weighted mean of 578.3 ± 3.5 Ma. Baddeleyite from a phoscorite dyke provides a concordant age of 580.25 ± 0.87 Ma for the crystallization of the dykes associated with the St-Honoré intrusive complex. Paleomagnetic results from the intrusion itself and related carbonatite and lamprophyre dykes exhibit some streaking between higher to moderate inclination directions, even at the site level, after screening to remove a steep, present-day viscous remanence. The predominant St-Honoré mean direction (13 sites), which is primary (baked contact test on the host Lac St-Jean anorthosite), is D = 119, I = 72.3°; ?95 = 9.5°, retained at higher coercivity and to high unblocking temperatures by titanomagnetite. Assuming a geocentric axial dipole, this result places the St. Honoré locality at 57° S at ~ 580 Ma, implying that Laurentia straddled mid-paleolatitudes at that time. Notably, the paleopole location at 27.2° N, 320.7 E (dp = 15°, dm = 17°) is consistent with similar mid-Ediacaran age paleopoles which place Laurentia at mid- to high paleolatitudes. The Saint-Honoré result implies that Laurentia had moved from low latitude in the early Ediacaran to higher southern paleolatitudes by 580-570 Ma, and then back to low paleolatitudes by as early as 564 Ma. Viewed as apparent polar wander (APW), this motion traces an 'Ediacaran loop' that can also be seen in similar-aged paleomagnetic results from at least two other paleocontinents. The similar APW loops suggest a role for true polar wander in Ediacaran geodynamics, and perhaps help to define a longitudinally-constrained global Ediacaran paleogeography.
Abstract: Kimberlites often entrain crustal felsic xenoliths, which show alteration and metamorphism as a result of interaction with the host kimberlite. We studied granite and gneiss xenoliths in the Renard 65 kimberlite pipe (Northern Québec, Canada). The study comprised a detailed petrographic examination of 45 thin sections, a scanning electron microscopy and an X-ray powder diffractometry of a sample sub-set. Two major units of the Renard 65 pipe (Unit A and Unit B/D) distinguished by abundance of crustal xenoliths along with the degree of their alteration, were investigated. Unit A is a volcaniclastic kimberlite with 40-90 % xenoliths, whereas Unit B/D is a hypabyssal kimberlite with textures transitional to pyroclastic, containing 15-40 % more intensely altered xenoliths. Both units carry xenoliths of coarse-grained leucogranite (K-feldspar, plagioclase, quartz, biotite with accessory garnet, apatite, and zircon) and medium-grained gneiss (plagioclase, quartz, biotite, orthopyroxene with accessory garnet, apatite and zircon). The Unit A xenoliths are partially replaced by chlorite, sericite, epidote, serpentine, richterite, actinolite and clinochlore vermiculite. In Unit B/D four distinct metamorphic and metasomatic mineral assemblages almost completely replace xenoliths. The assemblages include aegirine, pectolite, garnet, wollastonite, xonotlite, prehnite, calcite, K-feldspar and richterite in various proportions. Secondary K-feldspar and calcite may indicate the granite protolith, whereas wollastonite may be the signature of the gneiss protolith. The presence of secondary garnet and wollastonite, the hallmark skarn minerals, suggests the analogy between the classical skarn geological processes at the contact between felsic rocks and the host hot carbonate-rich melts. The observed mineralogy of the Renard 65 felsic xenoliths will be compared with the theoretically predicted mineralogy modelled using Theriak-Domino or Perplex software for the known bulk hybrid kimberlite compositions. The comparison will enable constraints on temperatures, volatile contents and thermal history of the kimberlite melt during emplacement.
Canadian Journal of Earth Science, Vol. 56, pp. 957-969.
Canada, Quebec, Labrador
REE
Abstract: A study of rare metal indicator minerals and glacial dispersal was carried out at the Strange Lake Zr?-?Y?-?heavy rare earth element deposit in northern Quebec and Labrador, Canada. The heavy mineral (>3.2 specific gravity) and mid-density (3.0-3.2 specific gravity) nonferromagnetic fractions of mineralized bedrock from the deposit and till up to 50 km down ice of the deposit were examined to determine the potential of using rare earth element and high fileld strength element indicator minerals for exploration. The deposit contains oxide, silicate, phosphate, and carbonate indicator minerals, some of which (cerianite, uraninite, fluorapatite, rhabdophane, thorianite, danburite, and aeschynite) have not been reported in previous bedrock studies of Strange Lake. Indicator minerals that could be useful in the exploration for similar deposits include Zr silicates (zircon, secondary gittinsite (CaZrSi2O7), and other hydrated Zr±Y±Ca silicates), pyrochlore ((Na,Ca)2Nb2O6(OH,F)), and thorite (Th(SiO4))/thorianite (ThO2) as well as rare earth element minerals monazite ((La,Ce,Y,Th)PO4), chevkinite ((Ce,La,Ca,Th)4(Fe,Mg)2(Ti,Fe)3Si4O22), parisite (Ca(Ce,La)2(CO3)3F2), bastnaesite (Ce(CO3)F), kainosite (Ca2(Y,Ce)2Si4O12(CO3)•H2O), and allanite ((Ce,Ca,Y)2(Al,Fe)3(SiO4)3(OH)). Rare metal indicator minerals can be added to the expanding list of indicator minerals that can be recovered from surficial sediments and used to explore for a broad range of deposit types and commodities that already include diamonds and precious, base, and strategic metals.
Abstract: We have investigated a locality very well known to mineral collectors, the Yates U-Th prospect near Otter Lake, Québec. There, dikes of orange to pink calcite enclose euhedral prisms of fluorapatite, locally aligned. Early investigators pointed out the importance of micro-inclusions in the prisms. We describe and image the micro-inclusions in two polished sections of fluorapatite prisms, one of them with a millimetric globule of orange calcite similar to that in the matrix. We interpret the globule to have been an inclusion of melt trapped during growth. Micro-globules disseminated in the fluorapatite are interpreted to have crystallized in situ from aliquots of the boundary-layer melt enriched in constituents rejected by the fluorapatite; the micro-globules contain a complex jigsawed assemblage of carbonate, silicate, and sulfate minerals. Early minerals to crystallize are commonly partly dissolved and partly replaced by lower-temperature phases. Such jigsawed assemblages seem to be absent in the carbonate matrix sampled away from the fluorapatite prisms. The pressure and temperature attained at the Rigolet stage of the Grenville collisional orogeny were conducive to the anatexis of marble in the presence of H2O. The carbonate melt is considered to have become silicocarbonatitic by assimilation of the enclosing gneisses, which were also close to their melting point. Degassing was important, and the melt froze quickly. The evidence points to a magmatic origin for the carbonate dikes and the associated clinopyroxenite, rather than a skarn-related association.
The Canadian Geographer, https://doi.org/ 10.1111/cag.12603
Canada, Quebec
legal
Abstract: This paper highlights the relevance of analyzing entangled territorialities and Indigenous use of maps in order to better understand what Lévy describes in terms of “spatial capital”—the socio?economic dynamics and power relationships maintained and negotiated between the stakeholders interacting within the Indigenous forestland. More specifically, it discusses the entanglement dynamics of land tenures coexisting today within Nitaskinan, the ancestral territory claimed by the Atikamekw Nehirowisiwok. Within Nitaskinan, members of the First Nation negotiate the continuity of their practices, occupation, and use of ancestral hunting territories with state institutions, logging companies, and non?Indigenous members of civil society who have interests in the land resources. All these stakeholders implement different territorial regimes that interact and sometimes conflict. Based on concrete ethnographic examples, the analysis presented here focuses on the compromises, frictions, resistance, and creativity that are part of territorial coexistence between Indigenous and non?Indigenous people. This paper is about the entanglement of Indigenous and state's land tenures in a Canadian context. The study highlights the relevance of analyzing entangled territorialities to better understand the power relationships within Indigenous forestland. The study demonstrates the complex articulations between domination and resistance dynamics in Indigenous mapping in a territorial negotiation process. This paper is about the entanglement of Indigenous and state's land tenures in a Canadian context. The study highlights the relevance of analyzing entangled territorialities to better understand the power relationships within Indigenous forestland. The study demonstrates the complex articulations between domination and resistance dynamics in Indigenous mapping in a territorial negotiation process.
The Canadian Mineralogist, Vol. 56, pp. 267-286. pdf
Canada, Quebec
deposit - Certac
Abstract: Xenoliths and xenocrysts of mantle material from kimberlite dikes located underground at the Certac Au mine, Québec, in the eastern Superior Craton, were studied in terms of the major element composition of their constituent minerals. The kimberlite was dated at 1151 ± 46 Ma by the U-Pb perovskite method. This suite thus provides a rare glimpse into the Mesoproterozoic mantle of the Superior Craton. Two parageneses of mantle material unrelated to the kimberlite magmatism occur: (1) an olivine + ilmenite ± magnetite association characterized by relatively Fe-rich olivine (Mg# = 0.68-0.84) and ilmenite enriched in Mg and Cr (4-13 wt.% MgO, Cr2O3 up to 3 wt.%), and (2) spinel peridotite characterized by Mg-rich olivine (Mg# = 0.91-0.94). The Fe-rich association is interpreted as a magmatic cumulate likely unrelated to the kimberlite. No mantle-derived garnet occurs in the xenoliths or as xenocrysts. The presence of Cr-rich spinel (Cr# = 0.84-0.98) in high temperature (860-953 °C) chromite peridotite indicates bulk compositions too depleted in Al for garnet to be stable, although geothermometry suggests they equilibrated at depths corresponding to garnet stability (90-131 km, depending on the geothermal gradient). Alternatively, the presence of phlogopite in two of the three high temperature (i.e., deepest) chromite peridotites suggests the absence of garnet and presence of low-Al chromite may have been caused by metasomatism from a K-rich fluid that replaced garnet with phlogopite + clinopyroxene ± chromite. Less depletion at shallower depths is indicated by a chromite (Cr# = 0.60) dunite that equilibrated at 831 °C and a low temperature (752 °C) Mg-Al-spinel lherzolite.
The Canadian Mineralogist, Special Publication 14, 634p.
Canada, Quebec
Book
Abstract: This paper introduces a special section of the Canadian Journal of Development Studies, "The Africa Mining Vision: A Manifesto for More Inclusive Extractive Industry-Led Development?" Conceived by African ministers "in charge of mineral resources" with inputs and guidance from African Union Heads of State, the Africa Mining Vision (AMV) was officially launched in February 2009. The papers presented in this special section reflect critically on progress that has since been made with operationalising the AMV at the country level across Africa; the general shortcomings of the manifesto; and the challenges that must be overcome if the continent is to derive g Taking over 20 years of meticulous preparation, László and Elsa Horváth, a duo of dedicated and dynamic amateur mineralogists, along with two researchers, Robert Gault, a mineralogist, and Glenn Poirier, a geologist, have produced the ultimate book "Mont Saint-Hilaire: History, Geology, Mineralogy". The photography captures the colors of Vásárely, the symmetry of Escher, the form of Bartók and the intricate patterns of Mandelbrot, all found here, in this miracle of nature. One cannot but marvel at how this single, small quarry contains such mineral diversity. At last count, over 434 mineral species have been found at Mont Saint-Hilaire, representing 9% of all known mineral species. The 66 type minerals first described from this locality represent 1.3 % of all mineral species, placing the Poudrette quarry in an extremely rarified class for worldwide mineral localities. Almost half, 47, of all known chemical elements are included in this mineral mix. Beginning some 124 million years ago, several million years and a variety of geological processes were needed to accomplish this assemblage. Be captivated, learn and, most of all, enjoy!reater economic benefit from its abundant mineral wealth.
Abstract: The oval-shaped basin of Hudson Bay occurs near the center of the round-oval Archaean crustal domain of the North American continent. This paper presents models of the geological structure and evolution of the subcontinental lithospheric mantle underlying Hudson Bay and surrounding tectonic provinces based on geological interpretations of regional geological and geophysical data and results of seismic tomography investigations that have been conducted under the Hudson Bay Lithospheric Experiment. The experiment was aimed at lithospheric processes directly related to the origin of the North American craton and the Hudson Bay basin. Hudson Bay is located directly above the lithospheric keel of North America. The geological history demonstrates systematic "renovation" of the basin: (1) origin and evolution of the Neoarchaean Lake Minto basin (~2.75 Ga); (2) accumulation of the Palaeoproterozoic volcanic-sedimentary filling of the epicontinental basin, relics of which is preserved on its passive margins (2.03-1.87 Ga); (3) origin of Ordovician-Late Devonian sedimentary sequence whose maximum thickness reaches 2.5 km; and (4) the development of Late Jurassic-Miocene sediment-filled ring-shaped trough immediately above the lithospheric keel. The Hudson Bay basin occurs above the lithospheric keel in compliance with thermomechanical model of ascending plume. Tomography studies have not detected evidence of either production or transformation of the lithosphere in the Palaeoproterozoic, which are implied by the model of the United Plates of America. Interpretations of tomography data reveal a vertical axial zone in the lithosphere beneath Hudson Bay, which extends from the lithosphere-asthenosphere boundary to the base of the crust or, perhaps, even to the present day surface. The zone is made up of relatively light low-velocity igneous rocks, probably a swarm of kimberlite dikes or pipes. At 2.75 Ga, the North American continent was a single continental mass with Hudson Bay at its center.
Abstract: There are lingering questions about how far back in geologic time plate tectonic processes began. In the Paleoproterozoic of eastern Laurentia, accretion of intra-oceanic juvenile terranes along the leading edge of the Superior craton apex (Ungava indenter) during the interval 1.87-1.83 Ga was followed by collision with the Churchill plate at ca. 1.83-1.79 Ga. Orthogonal shortening along the indenter led to early obduction of the juvenile terranes including the ca. 2.0 Ga Watts Group ophiolite, followed by out-of-sequence thrusting at ca. 1.83 Ga of granulite-facies crystalline basement of the Sugluk block (Churchill plate) along the Sugluk suture. Exhumation and erosion of the Sugluk block led to deposition of a foreland/delta fan sequence in the Hudson Bay re-entrant (Omarolluk and Loaf formations of the Belcher Group), with detritus sourced exclusively from the Sugluk block. Continued collision led to critical wedge development and orocline formation in the Hudson Bay re-entrant, forming a strongly arcuate fold-thrust belt. On the other (eastern) side of the indenter, material flow during crustal shortening was accommodated by lateral extrusion of microplates towards a then open ocean basin, in a manner similar to present-day extrusion of Indochina as a response to India - South China craton convergence. In the Churchill plate hinterland W-NW of the indenter, propagating strike-slip faults resulted in the far-field extrusion and oblique exhumation of Archean crustal slices of the Rae crustal block. The 1.83-1.79 Ga Superior-Churchill collision accommodated a minimum of 500 km of continent-continent convergence, with resulting style and mechanisms of orogenic growth and material flow similar to those observed in the Alpine-Himalayan orogenic system.
Journal of Metamorphic Geology, doi:10.1111/jmg.12599
Canada, Quebec
cratons
Abstract: Dating the onset of continental collision is fundamental in defining orogenic cycles and their effects on regional tectonics and geodynamic processes through time. Part of the Palaeoproterozoic Trans?Hudson Orogen, the Southeastern Churchill Province (SECP) is interpreted to result from the amalgamation of Archean to Palaeoproterozoic crustal blocks (amalgamated as the central Core Zone) that diachronically collided with the margins of the North Atlantic and Superior cratons, resulting in two bounding transpressive orogens: the Torngat and New Quebec Orogens. The SECP exposes mainly gneissic middle to lower orogenic crust in which deformation and amphibolite to granulite facies metamorphism and anatexis overprinted the early geological features classically used to constrain the timing of collisional events. To enable improved tectonic models for the development of the SECP, and the Trans?Hudson as a whole, we investigated granulite facies supracrustal sequences from the Tasiuyak Complex (TC) accretionary prism and the western margin of the North Atlantic Craton-that is, Saglek Block (upper plate)-using a multi?chronometer approach coupled with trace element geochemistry. In particular, the use of garnet Lu-Hf geochronology provides an important minimal time constraint for crustal thickening and collision. Garnet growth in the TC is constrained at 1885 ± 12 Ma (Lu-Hf), indistinguishable from U-Pb age of prograde monazite at 1873 ± 5 Ma. Zircon growth during melt crystallization occurred at 1848 ± 12 Ma. Garnet from the overriding Saglek Block is dated at 2567 ± 4.4 Ma (Lu-Hf) and indicates that gneissic rocks from the upper plate did not record the metamorphic imprint of the Torngat Orogeny. The diachronicity of the integrated metamorphic record across the strike of the SECP is explained by the location of terrane boundaries, consistent with the westward growth of the Churchill plate margin through sequential amalgamation of narrow crustal blocks during accretionary tectonics from c. 1.9 to 1.8 Ga.
Geology of Ore Deposits, Vol. 62, 8, pp. 704-718. pdf
Russia, Canada, Quebec
Mineralogy
Abstract: The chemical diversity of minerals can be analyzed in terms of the concept of mineral systems based on the set of chemical elements that are essential for defining a mineral species. Only species-defining elements are considered to be essential. According to this approach, all minerals are classified into ten types of mineral systems with the number of essential components ranging from 1 to 10. For all known minerals, only 70 chemical elements act as essential species-defining constituents. Using this concept of mineral systems, various geological objects may be compared from the viewpoint of their mineral diversity: for example, alkali massifs (Khibiny and Lovozero in Russia; Mont Saint Hilaire in Canada), evaporite deposits (Inder in Kazakhstan and Searles Lake in the United States), fumaroles of active volcanoes (Tolbachik in Kamchatka and Vulcano in Sicily, Italy), and hydrothermal deposits (Otto Mountain in the United States and El Dragon in Bolivia). Correlations between chemical and structural complexities of the minerals were analyzed using a total of 5240 datasets on their chemical compositions and 3989 datasets on their crystal structures. The statistical analysis yields strong and positive correlations (R2 > 0.95) between chemical and structural complexities and the number of different chemical elements in a mineral. The analysis of relationships between chemical and structural complexities provides strong evidence for the overall trend of a greater structural complexity at a higher chemical complexity. Following R. Hazen, four groups of minerals representing four mineral evolution stages have been considered: (I) “Ur-minerals,” (II) minerals from chondrite meteorites, (III) Hadean minerals, and (IV) contemporary minerals. According to the obtained data, the number of species-defining elements in minerals and their average contents increase regularly and significantly from stage I to stage IV. The analyzed average chemical and structural complexities in these four groups demonstrate that both are gradually increasing in the course of mineral evolution. The increasing complexity follows an overall trend: the more complex minerals were formed in the course of geological time, without replacing the simpler ones. The observed correlations between chemical and structural complexities understood in terms of the Shannon information suggest that chemical differentiation is the major force that drives the increase of mineral complexity over the course of geological time.
Contributions to Mineralogy and Petrology, Vol. 176, 10, 28p. Pdf
Canada, Quebec
deposit - Renard
Abstract: This study aims to constrain the nature of kimberlite-xenolith reactions and the fluid origin for Kimberley-type pyroclastic kimberlite (KPK). KPKs are characterized by an abundance of basement xenoliths (15-90%) and display distinct pipe morphology, textures, and mineralogy. To explain the KPK mineralogy deviating from the mineralogy of crystallized kimberlite melt, we study reactions between hypabyssal kimberlite transitional to KPK and felsic xenoliths. Here, we characterize the pectolite-diopside-phlogopite-serpentine-olivine common zonal patterns using petrography, bulk composition, thermodynamic modelling, and conserved element ratio analysis. To replicate the observed mineral assemblages, we extended the thermodynamic database to include pectolite, using calculated density functional theory methods. Our modelling reproduces the formation of the observed distinct mineralogy in reacted granitoid and gneiss. The assimilation of xenoliths is a process that starts from high temperatures (1200-600 °C) with the formation of clinopyroxene and wollastonite, continues at 600-200 °C with the growth of clinopyroxene, garnet, and phlogopite finishing at temperatures?
Abstract: Potential environmental issues associated with the mining of carbonatites are receiving increased attention due to the importance of critical metals for green technologies. This study investigates the chemistry of tailings seepage at the former Saint Lawrence Columbium mine near Oka, Québec, Canada, which produced pyrochlore concentrate and ferroniobium from a carbonatite-hosted Nb-REE deposit. Detailed field sampling and laboratory methods were used to characterize the hydraulic properties of the tailings, their bulk chemistry, mineralogy, pore water and effluent chemistries. The tailings are composed of REE-enriched calcite (64-89 wt %) and fluorapatite (2-22 wt %), as well as biotite (6-17 wt %) and chlorite (0-7 wt %). Minor minerals include ankerite, pyrite, sphalerite, molybdenite, magnetite and unrecovered pyrochlore. Secondary minerals include gypsum, barite, strontianite and rhodochrosite. Geochemical mass balance modeling, constrained by speciation modeling, was used to identify dissolution, precipitation and exchange reactions controlling the chemical evolution of pore water along its flow path through the tailings impoundment. In the unsaturated zone, these reactions include sulfide oxidation and calcite dissolution with acid neutralization. Below the water table, gypsum dissolution is followed by sulfate reduction and FeS precipitation driven by the oxidation of organic carbon in the tailings. Incongruent dissolution of biotite and chlorite releases K, Mg, Fe, Mn, Ba and F and forms kaolinite and Ca-smectite. Cation exchange reactions further remove Ca from solution, increasing concentrations of Na and K. Fluoride concentrations reach 23 mg/L and 8 mg/L in tailings pore water and effluent, respectively. These values exceed Canadian guidelines for the protection of aquatic life. In the mildly alkaline (pH 8.3) pore waters, Mo is highly mobile and reaches an average concentration of 83 ?g/L in tailings effluent, which slightly exceeds environmental guidelines. Concentrations (unfiltered) of Zn reach 1702 ?g/L in tailings pore water although values in effluent are usually less than 20 ?g/L. At the ambient pH, Zn is strongly adsorbed by Fe-Mn oxyhydroxides. Although U forms mobile complexes in tailings pore water, concentrations do not exceed 16 ?g/L due to the low solubility of its pyrochlore host. Adsorption and the low solubility of pyrochlore limit concentrations of Nb to less than 49 ?g/L. Cerium, from calcite dissolution, is strongly adsorbed although it reaches concentrations (unfiltered) in excess of 1 mg/L and 100 ?g/L in pore water and effluent, respectively. Results of this study show that mine tailings from carbonatite deposits are enriched in a wide variety of incompatible elements with multiple mineral hosts of varying solubility. Some of these elements, such as F and Mo, may represent contaminants of concern because of their mobility in alkaline tailings waters.
Abstract: Assimilation of country rock xenoliths by the host kimberlite can result in the development of concentric reaction zones within the xenoliths and a reaction halo in the surrounding contaminated kimberlite. Petrographic and geochemical changes across the reaction zones in the xenoliths and the host kimberlite were studied using samples with different kimberlite textures and contrasting xenolith abundances from the Renard 65 kimberlite pipe. The pipe, infilled by Kimberley-type pyroclastic (KPK) and hypabyssal kimberlite (HK) and kimberlite with transitional textures, was emplaced into granitoid and gneisses of the Superior Craton. Using samples of zoned, medium-sized xenoliths of both types, mineralogical and geochemical data were collected across xenolith-to-kimberlite profiles and contrasted with those of fresh unreacted country rock and hypabyssal kimberlite. The original mineralogy of the unreacted xenoliths (potassium feldspar-plagioclase-quartz-biotite in granitoid and plagioclase-quartz-biotite-orthopyroxene in gneiss) is replaced by prehnite, pectolite, and diopside. In the kimberlite halo, olivine is completely serpentinized and diopside and late phlogopite crystallized in the groundmass. The xenoliths show the progressive degrees of reaction, textural modification, and mineral replacement in the sequence of kimberlite units KPK — transitional KPK — transitional HK. The higher degree of reaction observed in the HK-hosted xenoliths as compared to the KPK-hosted xenoliths in this study and elsewhere may partly relate to higher temperatures in xenoliths included in an HK melt. The correlation between the degree of reaction and the kimberlite textures suggests that the reactions are specific to and occur within each emplaced batch of magma and cannot result from external post-emplacement processes that should obliterate the textural differences across the kimberlite units. Xenolith assimilation may have started in the melt, as suggested by the textures in the xenoliths and the surrounding halos and proceeded in the subsolidus. Elevated CaO at the kimberlite-xenolith contact appears to be an important factor in producing the concentric mineralogical zoning in assimilated xenoliths.
Abstract: Assimilation of country rock xenoliths by the host kimberlite can result in the development of concentric reaction zones within the xenoliths and a reaction halo in the surrounding contaminated kimberlite. Petrographic and geochemical changes across the reaction zones in the xenoliths and the host kimberlite were studied using samples with different kimberlite textures and contrasting xenolith abundances from the Renard 65 kimberlite pipe. The pipe, infilled by Kimberley-type pyroclastic (KPK) and hypabyssal kimberlite (HK) and kimberlite with transitional textures, was emplaced into granitoid and gneisses of the Superior Craton. Using samples of zoned, medium-sized xenoliths of both types, mineralogical and geochemical data were collected across xenolith-to-kimberlite profiles and contrasted with those of fresh unreacted country rock and hypabyssal kimberlite. The original mineralogy of the unreacted xenoliths (potassium feldspar-plagioclase-quartz-biotite in granitoid and plagioclase-quartz-biotite-orthopyroxene in gneiss) is replaced by prehnite, pectolite, and diopside. In the kimberlite halo, olivine is completely serpentinized and diopside and late phlogopite crystallized in the groundmass. The xenoliths show the progressive degrees of reaction, textural modification, and mineral replacement in the sequence of kimberlite units KPK — transitional KPK — transitional HK. The higher degree of reaction observed in the HK-hosted xenoliths as compared to the KPK-hosted xenoliths in this study and elsewhere may partly relate to higher temperatures in xenoliths included in an HK melt. The correlation between the degree of reaction and the kimberlite textures suggests that the reactions are specific to and occur within each emplaced batch of magma and cannot result from external post-emplacement processes that should obliterate the textural differences across the kimberlite units. Xenolith assimilation may have started in the melt, as suggested by the textures in the xenoliths and the surrounding halos and proceeded in the subsolidus. Elevated CaO at the kimberlite-xenolith contact appears to be an important factor in producing the concentric mineralogical zoning in assimilated xenoliths.
