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The Sheahan Diamond Literature Reference Compilation - Scientific and Media Articles based on Major Keyword - Alkaline Rocks
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 Keyword 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 an effort to make it easier for users to track down articles related to a specific topic, KRO has extracted these key words and developed a list of major key words presented in this Key Word Index to which individual key words used in the article reference have been assigned. In most of the individual Key Word Reports the references are in crhonological order, though in some such as Deposits the order is first by key word and then chronological. Only articles classified as "technical" (mainly scientific journal articles) and "media" (independent media articles) are included in the Key Word Index. References that were added in the most recent monthly update are highlighted in yellow.
Alkaline Rocks are rocks formed from magmas or fluids enriched with alkalis (potassium oxide and sodium oxide) relative to silica (silicon dioxide). When the magma is under-saturated with alkalis it is called "sub-alkaline". Alkaline rocks can be extrusive or intrusive. Although rare, they form a wide range of minerals. Alkaline rocks are relevant to diamonds because kimberlites and lamproites originate as alkaline magmas. They are especially relevant to rare earth minerals when they occur as carbonatites and syenites.
Strontium isotopic study of ultramafic nodules from neogene alkaline lavas of British Columbia, Canada and Josephine peridotite southwestern Oregon, USA
lead, Strontium, neodymium isotope studies of the 100-2700 Ma old alkalic rocks-carbonatite complexes in the Canadian Shield: inferences on the geochemical and structural evolution
Ph.D. Thesis, University of of California Santa Barbara,
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
Coupled substitutions involving REEs and Sodium and Silicon in apatites in Alkaline rocks from the Ilimaussaqintrusion, South Greenland, and the petrol.implication
American Mineralogist, Vol. 74, No. 7 and 8, July-August pp. 896-901
Compositional relations between natrolite, gonnardite, and thomsonite-products of nepheline alteration in alkaline rocks of the Magnet Cove igneouscomplex
Geological Society of America (GSA) Annual Meeting Abstracts, Vol. 21, No. 6, p. A326. Abstract
Compositional variations in pyroxenes and amphiboles of the Belknap Mountains complex, New Hampshire: evidence for the origin of silica-saturated alkaline rocks
American Mineralogist, Vol. 75, No. 9-10. Sept.-Oct. pp. 1092-1105
Temporal distribution of the ultramafic-alkalic and alkalic rocks withIn the Russian, Siberian and North American ancient platforms and theirsurroundings
Geological Survey of Wyoming Open File Report, No. 89-9, 33p
Mineralogy and geochemistry of perovskite- rich pyroxenites
Geological Association of Canada (GAC)/Mineralogical Association of Canada (MAC) Vancouver 90 Program with Abstracts, Held May 16-18, Vol. 15, p. A83. Abstract
Geochemical behaviour of rare earth elements in alterites of phosphate and titanium ore deposits in Tapira (Minas Gerais, Brasil):importance ofphosphates
Chemical Geology ( Geochem. of the Earth's surface and of min. formation, 2nd., Vol. 84, No. 1-4, July 5, pp. 377. Abstract
Brazil
Alkaline rocks, rare earth elements (REE) -phosphates
Gold bearing sulfide veins in shoshonites, formed by high -T, high -Clalkaline fluids, Prospector Mtn. Yukon Territory
Geological Association of Canada (GAC)/Mineralogical Association of Canada (MAC)/SEG Annual Meeting May 27-29. Toronto, Ontario, Abstract, Vol. 16, p. A46. Abstract
Conference registration The Canadian Institute of Mining, Metallurgy and Petroleum (CIM) Xerox Tower Suite 1210, 3400 de Maissoneuve, Sept. 5-13, 1991 Fax 514 939-2714
Mantle xenoliths in potassic magmas from Montana: Strontium, neodymium, and Osmium isotopic constraints on the evolution of the Wyoming craton lithosphere
Proceedings of Fifth International Kimberlite Conference held Araxa June, pp. 183-185
Alkaline hybrid mafic magmas of the Yampa area, northwest Colorado, and their relationship to the Yellowstone mantle plume and lithospheric mantle domains
Contributions to Mineralogy and Petrology, Vol. 107, No. 3, pp. 310-327
Potassic volcanism working group post congress excursion -volcanism in the Umbria-latium ultra alkaline district, Italy
International Conference on active volcanoes and risk mitigation, Field trip Sept. 2-, Department Scienze Della Terra, Piazza University of 06100 Perugia
Geology and petrology of Cerro Santo Tomas essexitic stock near locus typicus of the potassium-rich Guaira-Paraguari alkaline Province in easternParaguay.
Zentralblatt fur Geologie und Paleontologie, Vol. 1, 1991, No. 6, pp. 1773-1784.
samarium-neodymium (Sm-Nd) and Rubidium-Strontium ages of hornblende clinopyroxenite and metagabbro from the Lillebukt alkaline complex, Seiland Igneous Province.
Coexiting potassium-rich alkaline and shoshonitic magmatism of arc affinities In the Proterozoic: a reassessment of syenitic stocks in the southwestern GrenvilleProvince
Contribution to Mineralogy and Petrology, Vol. 113, pp. 262-279
International symposium on mineralization related to mafic and ultramafic rocks with a special session on alkaline and carbonatitic magmatism and associated min
Crscm-cnrs, To Be Held September 1-3, Orleans France,
Schmitt, H.R., Cameron, E.M., Hall, G.E.M., Viave, J.
Mobilization of gold into lake sediments from acid and alkaline mineralized environments in the southern Canadian shield: gold in lake sediments andnat.waters
Journal of Geochemical Exploration, Vol. 48, No. 3, August pp. 329-358
Proterozoic and Paleozoic a type granite suites in Labrador andNewfoundland: samarium-neodymium (Sm-Nd) evidence for the importance of juvenile sources.
Geological Association of Canada (GAC) Abstract Volume, Vol. 19, p.
rare earth elements (REE) distribution and rare earth elements (REE) carriers in laterites formed on the alkaline complexes of Araxa and Catalao, Brasil.
Compositional variations in clinopyroxenes from the Alno alkaline complex, east central Sweden: characterisation and implications for magmatic process.
18th. International Mineralogical Association Sept. 1-6, Edinburgh, abstract p.247.
Magma compositions and genesis of the rocks of the Mushugai Khuduk carbonatite bearing alkalic complex ( southern Mongolia): evidence from melt inclusions.
Periodico di Mineralogia, (in english), Vol. LXX11, 1. April, pp. 95-105.
Recognition of emplacement time of Jambil carbonatite complex from NW Pakistan: constraints from fission track dating of apatite using age standard approach.
GAC Annual Meeting Halifax May 15-19, Abstract 1p.
Abiogenic Fischer-Topsch synthesis of hydrocarbons in alkaline igneous rocks: fluid inclusions, textural and isotopic evidence from the Lovozero complex, NW Russia.
40Ar 39 Ar dates from alkaline intrusions in the northern Crazy Mountains, Montana: implications for the timing and duration of alkaline magmatism .. central
Veevers, J.J., Belousova, E.A., Saeed, A., Sircombe, K., Cooper, A.F., Read, S.E.
Pan Gondwanaland detrital zircons from Australia analysed for Hf isotopes and trace elements reflect an ice covered Antarctic provenance of 700-500 Ma ...
Earth Science Reviews, Vol. 76, 3-4, June pp. 135-174.
Oyhantcabal, P., Siegesmund, S., Wemmer K., Frei, R., Layer, P.
Post collisional transition from calc-alkaline to alkaline magmatism during transcurrent deformation in southernmost Dom Feliciano Belt ( Brazilian Pan-African
Plume related mantle source of super large rare metal deposits from the Lovozero and Khibin a massifs on the Kola Peninsula, east Baltic Shield: Sr, Nd, Hf isotope ssytematics.
Rogermitchellite, a new mineral species from Mont Hilaire Quebec: description, structure, determination and relationship with HFSE bearing cyclosilicates.
Lan, T-G., Fan, H-R., Santosh, M., Hu, F-F., Yang, Y-H, Liu, Y.
Geochemistry and Sr Nd Pb Hf isotopes of the Mesozoic Dadian alkaline intrusive complex in the Sulu orogenic belt, eastern China: implications for crust mantle interaction.
Lower crustal melting via magma underplating: elemental Sr Nd Pb isotopic constraints from late Mesozoic intermediate felsic volcanic rocks in NE Chin a block.
Geochemistry of alkaline basalts and associated high Mg basalts from the 2.7 Ga Penakacherla Terrane, Dharwar Craton, India: an Archean depleted mantle OIB array
Mineralogy of heavy minerals concentrates from the unconsolidated deposits of Eledoi and Pello Hill volcanic cones ( Gelai volcano): first preliminary data
Peralk-Carb 2011, workshop held Tubingen Germany June 16-18, Poster
Prelevic, D., Akal, C., Foley, S.F., Romer, R.R.,Stracke, A., Van den Bogaard, P.
Ultrapotassic mafic rocks as geochemical proxies for post collisional dynamics of orogenic lithospheric mantle: the case of southwestern Anatolia, Turkey.
Peralk-Carb 2011, workshop held Tubingen Germany June 16-18, Poster
Crystal chemistry of natural layered double hydroxides from the Kovdor alkaline massif, Kola. Polytypes of quininite: cation ordering and superstructures.
Peralk-Carb 2011, workshop held Tubingen Germany June 16-18, Poster
Azzone, R.G., Enrich, G.E.R., De Barros Gomes, C., Ruberti, E.
Trace element composition of parental magmas from mafic-ultramafic cumulates determined by in situ mineral analyses: the Juquia mafic-ultramafic alkaline-carbonatite massif, SE Brazil.
Journal of South American Earth Sciences, in press available, 17p.
Kazanskyite, Ba Ti Nb Na3 Ti (Si207) 202 (OH) 2 (H20)4, a group III Ti disilicate mineral from the Khibiny alkaline massif, Kola Peninsula, Russia: description and crystal structure.
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.
Eocene potassic magmatism of the Milk River area southern Alberta NTS 72E and Sweet Grass Hills, northern Montana: overview and new dat a on mineralogy, geochemistry, petrology and economic potential.
Alberta Geological Survey, Open file report 2012-01, 96p. Free pdf
Tretyachenko, W., Bovkun, A.V., Garanin, K.V., Garanin, V.K., Tretyachenko, N.G.
Formation features of the early Hercynic alkaline ultrabasic and basic volcanic complexes from Zimny Bereg area, north east of Archangelsk region, Russia.
10th. International Kimberlite Conference Held Bangalore India Feb. 6-11, Poster abstract
Baddeleyite trace element composition as a source of isotope geochemical and geochronological information about magmatic processes: Kovdor alkaline ultramafic massif as an example.
Abstract: Galena from four REE-rich (Khibina, Sallanlatvi, Seblyavr, Vuoriyarvi) and REE-poor (Kovdor) carbonatites, as well as hydrothermal veins (Khibina) all from the Devonian Kola Alkaline Province of northwestern Russia was analysed for trace elements and Pb and S isotope compositions. Microprobe analyses show that the only detectable elements in galena are Bi and Ag and these vary from not detectable to 2.23 and not detectable to 0.43 wt.% respectively. Three distinct galena groups can be recognized using Bi and Ag contents, which differ from groupings based on Pb isotope data. The Pb isotope ratios show significant spread with 206Pb/204Pb ratios (16.79 to 18.99), 207Pb/204Pb (15.22 to 15.58) and 208Pb/204Pb ratios (36.75 to 38.62). A near-linear array in a 207Pb/204Pb vs. 206Pb/204Pb ratio diagram is consistent with mixing between distinct mantle sources, one of which formed during a major differentiation event in the late Archaean or earlier. The S isotopic composition (?34S) of galena from carbonatites is significantly lighter (–-6.7 to -–10.3% Canyon Diablo Troilite (CDT) from REE-rich Khibina, Seblyavr and Vuoriyarvi carbonatites, and - 3.2% CDT from REE-poor Kovdor carbonatites) than the mantle value of 0%. Although there is no correlation between S and any of the Pb isotope ratios, Bi and Ag abundances correlate negatively with ?34S values. The variations in the isotopic composition of Pb are attributed to partial melting of an isotopically heterogeneous mantle source, while those of ?34S (together with Bi and Ag abundances) are considered to be process driven. Although variation in Pb isotope values between complexes might reflect different degrees of interaction between carbonatitic melts and continental crust or metasomatized lithosphere, the published noble gas and C, O, Sr, Nd and Hf isotopic data suggest that the variable Pb isotope ratios are best attributed to isotopic differences preserved within a sub-lithospheric mantle source. Different Pb isotopic compositions of galena from the same complex are consistent with a model of magma replenishment by carbonatitic melts/fluids each marked by quite different Pb isotopic compositions.
Abstract: The circular 625 km2 alkaline Pilanesberg Complex, South Africa, contains coeval eruptive and several distinctive intrusive syenitic and foyaitic components, concentrically arranged at the surface. However, owing to poor outcrop the relationships between the different intrusive rocks, and their shape in the third dimension cannot be convincingly determined in the field. The original interpretation was a laccolith, whereas later models suggested a funnel shape, and appealed to ring-dyke and cone-sheet emplacement mechanisms. However, the radial widths of these coarse-grained bodies are over 1 km and so cannot have been emplaced as ring dykes or cone sheets, which are usually quite thin and fine grained. Creating the space for emplacement and removal of pre-existing country rocks for each postulated subsequent intrusive event presents a major challenge to this latter hypothesis. Extensive previously published and new field relationships are re-evaluated here to suggest that the body is a gently inward-dipping sheet and that subsequent injections of magma merely pumped up an existing and evolving magma chamber rather than intruded into solid rocks. A Bouguer gravity anomaly model is presented that supports the concept of a shallow, flat-bottomed body rather than one that continues to significant depth. There are many analogies with the Kangerlussuaq Intrusion, Greenland.
Deep-seated magmatism, its sources and plumes, Proceedings of XIII International Workshop held 2014., Vol. 2014, pp. 124-147.
Baltic Shield, Fennoscandia
Carbonatite, alkaline rocks
Abstract: The paper presents the results of a study of the large Paleozoic ore-magmatic system in the northeastern Fennoscandian Shield comprising the Khibiny and Lovozero plutons, the Kurga intrusion, volcanic rocks, and numerous alkaline dike swarms. As follows from the results of deep drilling and 3D geophysical simulation, large bodies of rocks pertaining to the ultramafic alkaline complex occur at the lower level of the ore-magmatic system. Peridotite, pyroxenite, melilitolite, melteigite, and ijolite occupy more than 50 vol % of the volcanic-plutonic complex within the upper 15 km accessible to gravity exploration. The proposed model represents the ore-magmatic system as a conjugate network of mantle magmatic sources localized at different depth levels and periodically supplying the melts belonging to the two autonomous groups: (1) ultramafic alkaline rocks with carbonatites and (2) alkali syenites-peralkaline syenites, which were formed synchronously having a common system of outlet conduits. With allowance for the available isotopic datings and new geochronological evidence, the duration of complex formation beginning from supply of the first batches of melt into calderas and up to postmagmatic events, expressed in formation of late pegmatoids, was no less than 25 Ma.
Symposium on critical and strategic materials, British Columbia Geological Survey Paper 2015-3, held Nov. 13-14, pp. 83-90.
Europe, Greenland
Alkalic
Abstract: The Ilímaussaq alkaline complex is among the largest known alkaline complexes in the world and has been studied since the early 19th century, when Giesecke explored Greenland for minerals. More than 230 different mineral species occur in the complex. Ilímaussaq is the type locality for 34 minerals, including 15 that have not been reported elsewhere. Some of these are rock-forming minerals and thus, although unique to Ilímaussaq, may not be considered rare. Among the minerals fi rst described from Ilímaussaq are two important sources for critical materials: steenstrupine- (Ce) and eudialyte (Table 1). Steenstrupine-(Ce) is the main target mineral for the Kvanefjeld multi-element project in the northern part of Ilímaussaq, whereas eudialyte is targeted at the Tanbreez project in the southern part known as Kringlerne (Fig. 1). The fi rst detailed mapping and petrological studies of the complex were published by Ussing (1912), who also defi ned the term ‘agpaitic’ for rocks where the molar ratio (Na+K)/ Al is greater than or equal to 1.2. Since then, the distinction between agpaitic and miaskitic has changed from being based on just rock chemistry to being based more on mineral paragenesis. Sørensen (1997) defi ned agpaitic as peralkaline rocks in which High Field Strength Elements (HFSE; e.g., Zr and Ti) are hosted in complex minerals such as eudialyte and rinkite. Rocks with high alkalinity, where HFSE are hosted in minerals such as zircon, are considered miaskitic. Khomyakov (1995) further developed the agpaitic classifi cation by introducing the term hyperagpaitic for the most evolved syenites. Hyperagpaitic rocks are characterised by containing water soluble minerals (e.g., natrosilite and natrophosphate) and complex phosphosilicates (e.g., steenstrupine-(Ce) and vuonnemite; Khomyakov, 1995). The Ilímaussaq complex is one of several alkaline complexes formed during Mesoproterozoic rifting in the southwestern part of Greenland, which collectively is called the Gardar province (Upton, 2013). With an age of ~1.6 Ga, Ilímaussaq is the youngest major intrusion of the Gardar province (Waight et al., 2002; Krumrei et al., 2006).
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).
Tappe, S., Smart, K.A., Stracke, A., Romer, R.L., Prelevic, D., van den Bogaard, P.
Melt evolution beneath a rifted carton edge: 40Ar/39/Ar geochronology and Sr-Nd-Hf-Pb isotope systematics of primitive alkaline basalts and lamprophyres from the SW Baltic Shield.
Geochimica et Cosmochimica Acta, Vol. 173, pp. 1-36.
Abstract: The Quaternary Tasse basalts are exposed near the north shore of Quesnel Lake in southeastern British Columbia. They host a variety of mantle xenoliths consisting predominantly of spinel lherzolite with minor dunite and pyroxenite. Mineralogically, the xenoliths are composed of olivine, orthopyroxene, clinopyroxene and spinel characterized by forsterite (Fo87-93), enstatite (En90-92), diopside (En45-50-Wo40-45-Fs5), and Cr-spinel (6 ? 11 wt.% Cr), respectively. All of the mantle xenoliths are coarse-grained and show granoblastic textures. Clinopyroxene and spinel display textural evidence for chemical reactions with percolating melts. The mantle xenoliths are characterized by restricted Mg-numbers (89 ? 92) and low abundances of incompatible elements (Ba = 2 ? 11 ppm; Sr = 3 ? 31 ppm) and Yttrium (1 ? 3 ppm). On the basis of REE patterns, the xenoliths are divided into three groups reflecting the various degrees of mantle metasomatism: (1) Group 1 consists of concave-up LREE patterns (La/Smcn = 0.48 ? 1.16; Gd/Ybcn = 0.71 ? 0.92); (2) Group 2 possesses flat to moderately LREE-enriched patterns (La/Smcn = 1.14 ? 1.92; Gd/Ybcn = 0.87 ? 1.09); and (3) Group 3 is characterized by strongly LREE-enriched patterns (La/Smcn = 1.53 ? 2.45; Gd/Ybcn = 1.00 ? 1.32). On MORB-normalized trace element diagrams, the majority of the xenolith samples share the enrichment of LILE (Rb, Ba, K), U, Th, Pb, Sr and the depletion of HFSE (Nb, Ta, Ti, Y) relative to REE. These geochemical characteristics are consistent with a compositionally heterogeneous subcontinental lithospheric mantle source that originated as subarc mantle wedge peridotite at a convergent plate margin. The Tasse basalts have alkaline compositions characterized by low SiO2 (44 ? 46 wt.%) and high alkali (Na2O + K2O = 5.1 ? 6.6 wt.%) contents. They are strongly enriched in incompatible elements (TiO2 = 2.4 ? 3.1 wt.%; Ba = 580 ? 797 ppm; Sr = 872 ? 993 ppm) and, display OIB-like trace element patterns (La/Smn = 3.15 ? 3.85; Gd/Ybn = 3.42 ? 4.61). They have positive ?Nd (+ 3.8 to + 5.5) values, with 338 ? 426 Ma depleted mantle model ages, and display uniform OIB-like Sr (87Sr/86Sr = 0.703346 ? 0.703591) and Pb (206Pb/204Pb = 19.40 ? 19.58; 207Pb/204Pb = 15.57 ? 15.60; 208Pb/204Pb = 38.99 ? 39.14) isotopic compositions. The basalts erupted discontinuously along a > 1000 km long SE-NW-trending linear belt with minimal compositional variation indicative of a homogenous mantle source. The Sr ? Nd ? Pb isotope and trace element systematics of the alkaline basalts suggests that they originated from partial melting of an upwelling asthenospheric mantle source. Melting of the asthenospheric mantle might have stemmed from extension of the overlying lithosphere in response to the early stages of back-arc basin opening in the Omineca and Intermontane belts. Ridge subduction beneath the Canadian Cordillera might have played an important role in the weakening of the lithospheric mantle prior to its extension. Alternatively, melting of the upwelling asthenosphere in response to the delamination of the lithospheric mantle beneath the Rocky Mountain Trench might have generated the alkaline lavas.
Abstract: During Neoproterozoic Snowball Earth glaciations, the oceans gained massive amounts of alkalinity, culminating in the deposition of massive cap carbonates on deglaciation. Changes in terrestrial runoff associated with both breakup of the Rodinia supercontinent and deglaciation can explain some, but not all of the requisite changes in ocean chemistry. Submarine volcanism along shallow ridges formed during supercontinent breakup results in the formation of large volumes of glassy hyaloclastite, which readily alters to palagonite. Here we estimate fluxes of calcium, magnesium, phosphorus, silica and bicarbonate associated with these shallow-ridge processes, and argue that extensive submarine volcanism during the breakup of Rodinia made an important contribution to changes in ocean chemistry during Snowball Earth glaciations. We use Monte Carlo simulations to show that widespread hyaloclastite alteration under near-global sea-ice cover could lead to Ca2+ and Mg2+ supersaturation over the course of the glaciation that is sufficient to explain the volume of cap carbonates deposited. Furthermore, our conservative estimates of phosphorus release are sufficient to explain the observed P:Fe ratios in sedimentary iron formations from this time. This large phosphorus release may have fuelled primary productivity, which in turn would have contributed to atmospheric O2 rises that followed Snowball Earth episodes.
Abstract: Textural and compositional variations of apatite from four intrusions with different characteristic features of the rift-related alkaline Gardar Province were investigated: dyke rocks that belong to the most primitive rocks of the Province (Isortoq), nepheline-syenites associated with a carbonatite (Grønnedal-Ika), SiO2-saturated and SiO2-oversaturated syenites (Puklen) and nepheline-syenites displaying the transition from miaskitic to agpaitic mineral assemblages (Motzfeldt, Fig.1). Additionally, apatites from these intrusions were compared with other apatites of the Gardar Province. These include apatites from the Older Giant Dyke Complex, the Younger Giant Dyke Complex (both from the Tugtutôq region) and a narsarsukite-bearing trachytic dyke (Igdlutalik), as well as apatites from the Kûngnât, the North Qôroq and the Ilímaussaq intrusive complexes. This results in a complete overview of rift-related magmatites of the Gardar Province, ranging from primitive to highly evolved rocks. Backscattered electron images reveal the presence of various types of apatite textures including (i) growth zonation (concentric and oscillatory) that formed during magmatic differentiation and (ii) overgrowth and secondary textures (rounded cores, patchy zonation and overgrowth rims) due to fluid/melt induced metasomatic overprint and intracrystalline diffusion (Fig.2). Additionally, apatite compositions were analyzed with wavelength-dispersive electron microprobe analyses. During the crystallization history of the different intrusions, as well as within samples (documented by zoning patterns), increasing concentrations are observed for Si, REE, Na and F, whereas Cl shows a decreasing trend. However, for F, Cl and Na these trends are only observed in dyke rocks. Compositional variation of the investigated apatites is mainly due to substitution of Ca and P by variable amounts of Si, Na and REE. This study reveals that variations in the chemical composition of apatite are useful tools to obtain geochemical information about the host magma and its magmatic evolution. Here, Si and REE were found to be reliable petrogenetic indicators, whereas Na, F and Cl are only applicable in fast cooling systems to avoid redistribution of those elements.
Abstract: Igneous intrusions, notably carbonatitic-alkalic intrusions, peralkaline intrusions, and pegmatites, represent significant sources of rare-earth metals. Geophysical exploration for and of such intrusions has met with considerable success. Examples of the application of the gravity, magnetic, and radiometric methods in the search for rare metals are presented and described. Ground gravity surveys defining small positive gravity anomalies helped outline the shape and depth of the Nechalacho (formerly Lake) deposit within the Blatchford Lake alkaline complex, Northwest Territories, and of spodumene-rich mineralization associated with the Tanco deposit, Manitoba, within the hosting Tanco pegmatite. Based on density considerations, the bastnaesite-bearing main ore body within the Mountain Pass carbonatite, California, should produce a gravity high similar in amplitude to those associated with the Nechalacho and Tanco deposits. Gravity also has utility in modelling hosting carbonatite intrusions, such as the Mount Weld intrusion, Western Australia, and Elk Creek intrusion, Nebraska. The magnetic method is probably the most successful geophysical technique for locating carbonatitic-alkalic host intrusions, which are typically characterized by intense positive, circular to sub-circular, crescentic, or annular anomalies. Intrusions found by this technique include the Mount Weld carbonatite and the Misery Lake alkali complex, Quebec. Two potential carbonatitic-alkalic intrusions are proposed in the Grenville Province of Eastern Quebec, where application of an automatic technique to locate circular magnetic anomalies identified several examples. Two in particular displayed strong similarities in magnetic pattern to anomalies accompanying known carbonatitic or alkalic intrusions hosting rare-metal mineralization and are proposed to have a similar origin. Discovery of carbonatitic-alkalic hosts of rare metals has also been achieved by the radiometric method. The Thor Lake group of rare-earth metal deposits, which includes the Nechalacho deposit, were found by follow-up investigations of strong equivalent thorium and uranium peaks defined by an airborne survey. Prominent linear radiometric anomalies associated with glacial till in the Canadian Shield have provided vectors based on ice flow directions to source intrusions. The Allan Lake carbonatite in the Grenville Province of Ontario is one such intrusion found by this method. Although not discovered by its radiometric characteristics, the Strange Lake alkali intrusion on the Quebec-Labrador border is associated with prominent linear thorium and uranium anomalies extending at least 50 km down ice from the intrusion. Radiometric exploration of rare metals hosted by pegmatites is evaluated through examination of radiometric signatures of peraluminous pegmatitic granites in the area of the Tanco pegmatite.
Abstract: A new 190Pt-4He method for dating isoferroplatinum has been developed at the Institute of Precambrian Geology and Geochronology, Russian Academy of Sciences. Here we publish the first results of dating of isoferroplatinum from the main mineralogical and geochemical types of PGE mineralization in dunite. The obtained 190Pt-4He age of isoferroplatinum is 129 ± 6 Ma. The gained 190Pt-4He age of isoferroplatinum specimens of different genesis (magmatic, fluid-metamorphogenic, and metasomatic) from the Kondyor Massif indicates that the PGM mineralization took place synchronously and successively with evolution of primarily picrite, followed by subalkaline and alkaline melts of the Mesozoic tectonic-magmatic activation of the Aldan Shield.
Geochemistry: Exploration, Environment, Analysis, Vol. 16, 3-4, pp. 193-212.
Canada, Ontario
Alkalic
Abstract: Mineral exploration is increasingly taking advantage of real time techniques that dramatically reduce the costs and time taken to obtain results compared to traditional analytical methods. Portable X-ray fluorescence (pXRF) is now a well-established technique that is used to acquire lithogeochemical data. To date, however, benchtop scanning electron microscopes, equipped with energy dispersive systems (bSEM-EDS) have received little attention as a possible mineral exploration tool. This study examines the utility of combining pXRF and bSEM-EDS to characterize the igneous stratigraphy and its relationship to Cu-Pd mineralization in a drill hole at the Four Dams occurrence, located within the Eastern Gabbro assemblage of the Coldwell Alkaline Complex, Canada. The first part of this study compares field portable and laboratory techniques. Seventy-two powdered samples analysed by pXRF are compared with traditional major elements analysed by inductively coupled atomic emission spectroscopy (ICP-AES) and trace elements by inductively coupled plasma spectrometry (ICP-MS), and the compositions of 128 olivine, clinopyroxene and plagioclase grains analysed by bSEM-EDS are compared with traditional electron microprobe data. Our results show that each portable technique yields results similar to their lab-based counterparts within the analytical capabilities and precisions of the respective instruments. The second part presents a case study for the application of pXRF and bSEM-EDS to resolve questions related to igneous stratigraphy as an aid to mineral exploration in a complicated geological setting. A major problem for Cu-Pd exploration in the Coldwell Complex of NW Ontario is that the oxide-rich units that host Cu-Pd mineralization in the Marathon Series are petrographically similar to the barren oxide-rich units in the Layered Series. However, the mineralized units are geochemically distinctive. Our results show that the mineralized Marathon Series can be distinguished from the barren Layered Series, including oxide-rich units of both, by combinations of P2O5, Ba, Zr and V/Ti values, determined by pXRF, combined with plagioclase, olivine or clinopyroxene compositions measured by bSEM-EDS. The combination of pXRF and bSEM-EDS thus shows considerable promise as an exploration technique.
Abstract: The Burpala alkaline massif contains rocks with more than 50 minerals rich in Zr, Nb, Ti, Th, Be and rare earth elements (REE). The rocks vary in composition from shonkinite, melanocratic syenite, nepheline and alkali syenites to alaskite and alkali granite and contain up to 10% LILE and HSFE, 3.6% of REE and varying amounts of other trace elements (4% Zr, 0.5% Y, 0.5% Nb, 0.5% Th and 0.1% U). Geological and geochemical data suggest that all the rocks in the Burpala massif were derived from alkaline magma enriched in rare earth elements. The extreme products of magma fractionation are REE rich pegmatites, apatite-fluorite bearing rocks and carbonatites. The Sr and Nd isotope data suggest that the source of primary melt is enriched mantle (EM-II). We correlate the massif to mantle plume impact on the active margin of the Siberian continent.
Abstract: Highly evolved alkaline/peralkaline igneous rocks host deposits of rare earth elements (REE) including Y as well as Zr, Hf, Nb, Ta , U and Th. The host rocks spanning from silica-undersaturated (nepheline syenites) to silica-oversaturated (granites) occur in intraplate tectonic environments, mainly in continental settings and are typically associated with rifting, faulting and/or crustal extension. They range in age from Neoarchean/Paleoproterozoic to Mesozoic, but several significant deposits are of Mesoproterozoic age. The deposits/prospects can be subdivided into three types. The first is hosted by nepheline syenitic rocks of large, layered alkaline intrusions where the mineralization commonly occurs in layers rich in REE-bearing minerals which mostly show cumulate textures (e.g., Thor Lake/Nechalacho, Canada; Ilimaussaq, Greenland; Lovozero, Russia; Kipawa, Canada; Norra Kärr, Sweden; Pilanesberg, South Africa). The second type includes mineralization in peralkaline granitic rocks where REE-bearing minerals are usually disseminated. The mineralization is typically hosted by pegmatites (including the NYF-type), felsic dikes and minor granitic intrusions (e.g., Strange Lake, Canada; Khaldzan-Buregtey, Mongolia; Ghurayyah, Saudi Arabia; Bokan, Alaska, United States). The third type is disseminated and very fine-grained and hosted by peralkaline felsic volcanic/volcaniclastic rocks, mostly of trachytic composition (e.g., Dubbo Zirconia and Brockman/Hastings, Australia). The bulk of the REE is present in ore/accessory minerals which in some mineralized zones, particularly in cumulate rocks from alkaline complexes, can reach >10 vol.%. Mineralization is composed of a variety of REE-bearing minerals which frequently show complex replacement textures. They include fluorocarbonates, phosphates, silicates and oxides. Economically most important are bastnäsite, monazite, xenotime, loparite, eudialyte, synchysite and parasite. Many other minerals are either sparse or it is difficult with present technology to profitably extract REE from them on a commercial scale. Compared to carbonatite-hosted REE deposits, the REE mineralization in alkaline/peralkaline complexes has lower light REE concentrations but has commonly higher contents of heavy REE and Y and shows a relative depletion of Eu. Elevated concentrations of U and Th of the ore assemblages make gamma-ray (radiometric) surveys an important exploration tool. The host peralkaline (granitic, trachytic and nepheline syenitic) magmas undergo extensive fractional crystallization which is protracted in part due to high contents of halogens and alkalis. The REE mineralization in these rocks is related to late stages of magma evolution, and typically records two mineralization periods. The first produces the primary magmatic ore assemblages which are associated with the crystallization of fractionated peralkaline magma rich in rare metals. This assemblage is commonly overprinted during the second period by the late magmatic to hydrothermal fluids which remobilize and enrich the original ore. The parent magmas are derived from a metasomatically enriched mantle-related lithospheric source by very low degrees of partial melting triggered probably by uplift (adiabatic) or mantle plume activity. The rare metal deposits/mineralization related to peralkaline igneous rocks represent one of the most economically important resources of heavy REE including Y. In addition to REE, some of these deposits contain economically valuable concentrations of other rare metals including Zr, Nb, Ta, Hf, Be, U and Th as well as phosphates.
Journal of Volcanology and Geothermal Research, in press available 11p.
South America, Brazil
Alkaline rocks
Abstract: We report the first high-precision ID-TIMS U-Pb baddeleyite/zircon and 40Ar/39Ar step-heating phlogopite age data for diabase and lamprophyre dykes and a mafic intrusion (José Fernandes Gabbro) located within the Ponta Grossa Arch, Brazil, in order to constrain the temporal evolution between Early Cretaceous tholeiitic and alkaline magmatism of the Paraná-Etendeka Magmatic Province. U-Pb dates from chemically abraded zircon data yielded the best estimate for the emplacement ages of a high Ti-P-Sr basaltic dyke (133.9 ± 0.2 Ma), a dyke with basaltic andesite composition (133.4 ± 0.2 Ma) and the José Fernandes Gabbro (134.5 ± 0.1 Ma). A 40Ar/39Ar phlogopite step-heating age of 133.7 ± 0.1 Ma from a lamprophyre dyke is identical within error to the U-Pb age of the diabase dykes, indicating that tholeiitic and alkaline magmatism were coeval in the Ponta Grossa Arch. Although nearly all analysed fractions are concordant and show low analytical uncertainties (± 0.3-0.9 Ma for baddeleyite; 0.1-0.4 Ma for zircon; 2?), Pb loss is observed in all baddeleyite fractions and in some initial zircon fractions not submitted to the most extreme chemical abrasion treatment. The resulting age spread may reflect intense and continued magmatic activity in the Ponta Grossa Arch.
Journal of Asian Earth Sciences, Vol. 135, pp. 80-94.
China
Alkaline rocks
Abstract: In this paper, some potassic and ultrapotassic rocks in the South China Block (SCB) have been recognized, according to a set of new geochronological, geochemical and Sr-Nd isotopic data. Zircon U-Pb dating from six plutons yield consistent crystallization ages of 445-424 Ma. These potassic and ultrapotassic rocks can be geochemically subdivided into three groups. Group 1, represented by the Longchuan gabbro, longmu diabase, Tangshang and Danqian diorite (445-433 Ma), have low silica contents (SiO2 = 47.38-54.16 wt.%), and high MgO (4.21-9.51 wt.%) and total alkalis (Na2O + K2O = 3.08-5.57 wt.%), with K2O/Na2O ratios of 0.62-1.82. They are enriched in LREE and depleted in Ba, Sr and Ta-Nb-Ti, and exhibit relatively high initial 87Sr/86Sr ratios (0.70561-0.71128), low ?Nd(430 Ma) values (?8.4 to ?3.2), suggesting that they were most plausibly generated by the partial metling of enriched mantle source (EMI). Group 2, from the Huwei diorite (424 Ma), have 45.68-52.87 wt.% of SiO2, 5.79-9.25 wt.% of MgO and 52-65 of mg-number. They have significantly higher Th (9.92 ppm), Ce (88.0-115 ppm) concentration and Ce/Yb (27.6-46.8), Th/Yb ratios (2.58-7.99), and relatively low initial 87Sr/86Sr ratios (0.70501-0.70599), and high ?Nd(430 Ma) values (?2.1 to ?1.5). We propose that they originated from the partial melting of the depleted mantle source with subsequent contamination by crustal materials. Group 3, represented by the Daning lamprophyre (?445 Ma), has SiO2 contents ranging from 41.73 wt.% to 45.22 wt.%, MgO from 13.74 wt.% to 15.16 wt.%, and mg-muber from 73 to 77, with high K2O/Na2O ratios (>2.0). They have 87Sr/86Sr ratios of 0.62912-0.70384 and ?Nd(t = 430 Ma) values of ?6.4 to ?6.3, indicating that the source components are close to the EMI source, with significant sediments involved. These Silurian potassic and ultrapotassic rocks in the SCB can be responsible for post-orogenic delamination and intra-plate extension. And the delamination had a small size and a long duration, and a negligible impact.
Journal of African Earth Sciences, Vol. 129, pp. 202-223.
Africa, Morocco
Alkaline rocks
Abstract: The Jbel Boho complex (Anti-Atlas/Morocco) is an alkaline magmatic complex that was formed during the Precambrian-Cambrian transition, contemporaneous with the lower early Cambrian dolomite sequence. The complex consists of a volcanic sequence comprising basanites, trachyandesites, trachytes and rhyolites that is intruded by a syenitic pluton. Both the volcanic suite and the pluton are cut by later microsyenitic and rhyolitic dykes. Although all Jbel Boho magmas were probably ultimately derived from the same, intraplate or plume-like source, new geochemical evidence supports the concept of a minimum three principal magma generations having formed the complex. Whereas all volcanic rocks (first generation) are LREE enriched and appear to be formed by fractional crystallization of a mantle-derived magma, resulting in strong negative Eu anomalies in the more evolved rocks associated with low Zr/Hf and Nb/Ta values, the younger syenitic pluton displays almost no negative Eu anomaly and very high Zr/Hf and Nb/Ta. The syenite is considered to be formed by a second generation of melt and likely formed through partial melting of underplated mafic rocks. The syenitic pluton consists of two types of syenitic rocks; olivine syenite and quartz syenite. The presence of quartz and a strong positive Pb anomaly in the quartz syenite contrasts strongly with the negative Pb anomaly in the olivine syenite and suggests the latter results from crustal contamination of the former. The late dyke swarm (third generation of melt) comprises microsyenitic and subalkaline rhyolitic compositions. The strong decrease of the alkali elements, Zr/Hf and Nb/Ta and the high SiO2 contents in the rhyolitic dykes might be the result of mineral fractionation and addition of mineralizing fluids, allowing inter-element fractionation of even highly incompatible HFSE due to the presence of fluorine. The occurrence of fluorite in some volcanic rocks and the Ca-REE-F carbonate mineral synchysite in the dykes with very high LREE contents (Ce ?720 ppm found in one rhyolitic dyke) suggest the fluorine-rich nature of this system and the role played by addition of mineralizing fluids. The REE mineralization expressed as synchysite-(Ce) is detected in a subalkaline rhyolitic dyke (with ?LREE = 1750 ppm) associated with quartz, chlorite and occasionally with Fe-oxides. The synchysite mineralization is probably the result of REE transport by acidic hydrothermal fluids as chloride complex and their neutralization during fluid-rock interaction. The major tectonic change from compressive to extensional regime in the late Neoproterozoic induced the emplacement of voluminous volcaniclastic series of the Ediacran Ouarzazate Group. The alkaline, within-plate nature of the Jbel Boho igneous complex implies that this extensional setting continued during the early Cambrian.
International Journal of Earth Sciences, in press available 17p.
Africa, Namibia
Alkaline rocks
Abstract: Rb-Sr whole-rock and mineral isotope data from nepheline syenite, tinguaite, and carbonatite samples of the Kalkfeld Complex within the Damaraland Alkaline Province, NW Namibia, indicate a date of 242?±?6.5 Ma. This is interpreted as the age of final magmatic crystallization in the complex. The geological position of the complex and the spatially close relationship to the Lower Cretaceous Etaneno Alkaline Complex document a repeated channeling of small-scale alkaline to carbonatite melt fractions along crustal fractures that served as pathways for the mantle-derived melts. This is in line with Triassic extensional tectonic activity described for the nearby Omaruru Lineament-Waterberg Fault system. The emplacement of the Kalkfeld Complex more than 100 Ma prior to the Paraná-Etendeka event and the emplacement of the Early Cretaceous Damaraland intrusive complexes excludes a genetic relationship to the Tristan Plume. The initial ?Sr-?Nd pairs of the Kalkfeld rocks are typical of younger African carbonatites and suggest a melt source, in which EM I and HIMU represent dominant components.
Abstract: A quartzolite from the Rova occurrence, Keivy alkali granite province, Kola Peninsula, Russia, is used to examine the differing responses of certain rare-metal minerals during interaction with hydrothermal fluids. The minerals are two silicates [chevkinite-(Ce) and zircon], a phosphate [monazite-(Ce)] and an oxide [fergusonite-(Y)]. Textural evidence is taken to show that the dominant alteration mechanism was interface-coupled dissolution-reprecipitation. Zircon was the most pervasively altered, possibly by broadening of cleavage planes or fractures; the other minerals were altered mainly on their rims and along cracks. The importance of cracks in promoting fluid access is stressed. The compositional effects of the alteration of each phase are documented. The hydrothermal fluids carried few ligands capable of transporting significant amounts of rare-earth elements (REE), high field strength elements (HFSE) and actinides; alteration is inferred to have been promoted by mildly alkaline, Ca-bearing fluids. Expansion cracks emanating from fergusonite-(Y) are filled with unidentified material containing up to 35 wt% UO2 and 25 wt% REE2O3, indicating late-stage, short-distance mobility of these elements. Electron microprobe chemical dating of monazite yielded an age of 1665 ± 22 Ma, much younger than the formation age of the Keivy province (2.65-2.67 Ga) but comparable to that of the Svecofennian metamorphic event which affected the area (1.9-1.7 Ga) or during fluid-thermal activation of the region during rapakivi granite magmatism (1.66-1.56 Ga). Dates for altered monazite range from 2592 ± 244 Ma to 773 ± 88 Ma and reflect disturbance of the U-Th-Pb system during alteration.
Abstract: The Late Cretaceous Itatiaia complex is made up of nepheline syenite grading to peralkaline varieties, quartz syenite and granite, emplaced in the metamorphic rocks of the Serra do Mar, SE Brazil. The nepheline syenites are characterized by assemblages with alkali feldspar, nepheline, Fe-Ti oxides, clinopyroxene, amphibole, apatite and titanite, while the peralkaline nepheline syenites have F-disilicates (rinkite, wöhlerite, hiortdahlite, låvenite), britholite and pyrophanite as the accessory phases. The silica-oversaturated rocks have alkali feldspar, plagioclase, quartz, amphibole, clinopyroxene and Fe-Ti oxides; the chevkinite-group minerals are the featured accessory phases and are found with allanite, fluorapatite, fluorite, zircon, thorite, yttrialite, zirconolite, pyrochlore and yttrocolumbite. The major- and trace-element composition of the Itatiaia rocks have variations linked to the amount of accessory phases, have smooth, enriched chondrite-normalized rare-earth element (REE) distribution patterns in the least-evolved nepheline syenites and convex patterns in the most-evolved nepheline syenites. The REE distribution patterns of the quartz syenites and granites show a typical pattern caused by fractional crystallization of feldspar and amphibole, in an environment characterized by relatively high oxygen fugacity (>NiNiO buffer) and high concentrations of H2O and F, supporting the crystallization of hydrous phases, fluorite and F-disilicates. The removal of small amounts of titanite in the transition from the least-evolved to the most-evolved nepheline syenites stems from petrogenetic models involving REE, and is shown to be a common feature of the magmatic evolution of many other syenitic/ trachytic/ phonolitic complexes of the Serra do Mar and elsewhere.
Abstract: Accurate characterization of the platinum group mineral (PGM) assemblages for Cu-Ni-PGE deposits are typically constrained by sample size and the difficulty of finding statistically significant numbers of grains, which is expected given the low concentrations of platinum group elements (<2 ppm), the great variety of PGM, and the likelihood that a few large grains (>75 µm) can account for large fractions of total mass. Despite these limitations, an accurate survey of PGM from different deposit types would have significant value towards developing deposit models and respective exploration strategies. In this study, we present results for a comprehensive evaluation of PGM at four copper-PGE occurrences hosted within separate but co-genetic gabbro or troctolite intrusions in the Coldwell Alkaline Complex and confirm that accurate surveys are possible with sufficient sample material and efficient PGM concentration methods. The PGM concentration methods used include: (1) hydroseparation of sieved size fractions of pulverized material, and (2) panning of grain separates produced by electric pulse disaggregation of drill core specimens. A favourable comparison of the results has verified the reliability of each method and added confidence that the PGM assemblages identified at three of the four locations are fully characterized. Precious metal mineral (PMM) assemblages are determined for the Main zone and W Horizon at the Marathon deposit, and the main zones at each of the Geordie Lake deposit and Area 41 occurrence. A total of 10,824 PMM grains (PGE and Au-Ag) and 68 mineral species, including 16 unknown minerals, were identified, of which 768 grains and 31 species occur at the Main zone, 523 grains and 41 species at Area 41,9485 grains and 43 species at W horizon, and 56 grains and 12 species at Geordie Lake. The PMM are grouped as follows: Pd-Ge, PGE-S-As, Pt-Fe alloy, Pd-Cu-Pb-Au, Pd-Ni-S, Pd-Pt-Sn, Pt-As, Pd-As, Pd-Pt-Sb-As, Pd-Pt-Bi-Te, and Au-Ag. All of the deposits were found to contain similar proportions of Pd-Pt-Sb-As, Pd-Pt-Bi-Te and Au-Ag minerals. But the W Horizon and Area 41 are distinguished from the Marathon Main zone and Geordie Lake deposits by the presence of minerals in the PGE-S-As, Pt-Fe alloy, Pd ± Cu ± Pb ± Au and Pd-Ge groups. Taken together, the PMM assemblages for deposits in the Coldwell exhibit a strong correlation to PGE enrichment relative to the range for mantle Cu/Pd values (1000-10,000). And there is no relationship between the abundances of Pd-Pt-Bi-Te and Pd-Pt-Sb-As minerals that are commonly associated with hydrous phases, and the intensity of hydrothermal alteration. Thus minerals found only at the W Horizon and Area 41, where significant PGE upgrading has occurred, including Pt-Fe alloys, rustenburgite, marathonite, palladogermanide, unknown Rh-Ni-Fe-sulfide, Au-Pd-Cu alloy, braggite, coldwellite, laurite, zvyagintsevite, laflammeite, and unknown phases Pd5As2, Pd3As, Pd3(As,Pb,Bi) might be considered as index minerals for PGE enriched types of mineralization in the Coldwell.
Abstract: The W Horizon, Marathon Cu-Pd deposit in the Mesoproterozoic Midcontinent rift is one of the highest grade PGE repositories in magmatic ore deposits world-wide. The textural relationships and compositions of diverse platinum-group mineral (PGM) and sulfide assemblages in the extremely enriched ores (>100 ppm Pd-Pt-Au over 2 m) of the W Horizon have been investigated in mineral concentrates with ?10,000 PGM grains and in situ using scanning electron microprobe and microprobe analyses. Here we show, from ore samples with concentrations up to 23.1 Pd ppm, 8.9 Pt ppm, 1.4 Au ppm and 0.73 Rh ppm, the diversity of minerals (n = 52) including several significant unknown minerals and three new mineral species marathonite (Pd25Ge9; McDonald et al., 2016), palladogermanide (Pd2Ge; IMA 2016-086, McDonald et al., 2017), kravtsovite (PdAg2S, IMA No 2016-092, Vymazalová et al., 2017). The PGM are distributed as PG-, sulfides (52 vol%), -arsenides (34 vol%), -intermetallics of Au-Ag-Pd-Cu and Pd-Ge(10 vol%) and -bismuthides and tellurides (4 vol%). The discovery of abundant (>330 grains) large unknown sulfide minerals with Rh allows us to present analyses three significant potentially new minerals (WUK-1, WUK-2, WUK-3) that are all clearly enriched in Rh (averaging 4.2, 8.5 and 28.21 wt% Rh respectively). Several examples of paragenetic sequences and mineral chemical changes for enrichment of Cu, Pd and Rh with time are revealed in the PGM and base-metal sulfides. We suggest this enhanced metal enrichment formed in response to increasing fO2 causing the oxidation of Fe2+ to Fe3+ and to a lesser extent, S. Phase relations in the Ag-Pd-S, Rh-Ni-Fe-S, Pd-Ge, Au-Pd-Cu-Ag, Pd-Ag-Te systems help constrain the crystallization temperatures of the majority of ore minerals in the W Horizon at ?500 °C or moderate to high subsolidus temperatures (400–600 °C). Local transport by aqueous fluids becomes evident as minerals recrystallize down to <300 °C. The PGE-enriched W Horizon ores exhibit a complex post-magmatic history dominated by the effects of oxidation during cooling of a Cu-PGE enriched magma source from a deep reservoir.
Abstract: The Mesoproterozoic Pilanesberg Complex, South Africa, is built up by several distinct, ring-shaped intrusions of syenite and peralkaline nepheline syenite. A mildly peralkaline ((Na + K) / Al = 1.04–1.09), medium-to coarse grained nepheline syenite makes up the outermost ring in the southwestern part of the complex (“Matooster type white foyaite”). In this rock, mafic silicate minerals (amphibole, biotite, aegirine) and Ti-bearing minerals (ilmenite, astrophyllite, aenigmatite, lorenzenite, bafertisite, jinshajiangite) are interstitial to feldspar and nepheline, and define a series of mineral assemblages reflecting a change from a miaskitic crystallization regime (with Na-Ca amphibole, titanite and ilmenite) to increasingly agpaitic conditions (with arfvedsonite, aegirine, astrophyllite, aenigmatite, lorenzenite). The main driving force behind the evolution was an increase in peralkalinity of the trapped liquid, mainly by adcumulus growth of alkali feldspar and nepheline, which in the later stages of evolution was combined with increases in oxygen fugacity and water activity. Unlike in most other agpaitic rock complexes, Zr remained compatible in aegirine (and to some extent in amphibole) almost to the end of the process, when a hydrous zirconium silicate mineral (hilairite) crystallized as the only mineral in the rock having essential zirconium. The presence of minerals such as hilairite, bafertisite, jinshajiangite and a Na-REE-Sr rich apatite group mineral (fluorcaphite ?) in the latest assemblages suggests that the last remaining interstitial melt or fluid approached a hyperagpaitic composition. The isolated melt pockets in the Pilanesberg white foyaite follow a pattern of evolution that can be seen as a miniature analogue of the fractional crystallization processes controlling magma evolution in large, alkaline igneous rock complexes.
Journal of South American Earth Sciences, Vol. 77, pp. 286-309.
South America, Brazil
alkaline - Jacupiringa
Abstract: The Jacupiranga Complex is one of several Meso-Cenozoic alkaline intrusive complexes along the margins of the intracratonic Paraná Basin in southern Brazil. The complex encompasses a wide range of rock-types, including dunites, wehrlites, clinopyroxenites, melteigites-ijolites, feldspar-bearing rocks (diorites, syenites, and monzonites), lamprophyres and apatite-rich carbonatites. While carbonatites have been extensively investigated over the last decades, little attention has been paid to the silicate rocks. This study presents new geochonological and geochemical data on the Jacupiranga Complex, with particular emphasis on the silicate lithotypes. 40Ar/39Ar ages for different lithotypes range from 133.7 ± 0.5 Ma to 131.4 ± 0.5 Ma, while monzonite zircon analyzed by SHRIMP yields a U-Pb concordia age of 134.9 ± 1.3 Ma. These ages indicate a narrow time frame for the Jacupiranga Complex emplacement, contemporaneous with the Paraná Magmatic Province. Most of the Jacupiranga rocks are SiO2-undersaturated, except for a quartz-normative monzonite. Based on geochemical compositions, the Jacupiranga silicate lithotypes may be separated into two magma-evolution trends: (1) a strongly silica-undersaturated series, comprising part of the clinopyroxenites and the ijolitic rocks, probably related to nephelinite melts and (2) a mildly silica-undersaturated series, related to basanite parental magmas and comprising the feldspar-bearing rocks, phonolites, lamprophyres, and part of the clinopyroxenites. Dunites and wehrlites are characterized by olivine compositionally restricted to the Fo83-84 interval and concentrations of CaO (0.13–0.54 wt%) and NiO (0.19–0.33 wt%) consistent with derivation by fractional crystallization, although it is not clear whether these rocks belong to the nephelinite or basanite series. Lamprophyre dikes within the complex are considered as good representatives of the basanite parental magma. Compositions of calculated melts in equilibrium with diopside cores from clinopyroxenites are quite similar to those of the lamprophyres, suggesting that at least a part of the clinopyroxenites is related to the basanite series. Some feldspar-bearing rocks (i.e. meladiorite and monzonite) show petrographic features and geochemical and isotope compositions indicative of crustal assimilation, although this may be relegated to a local process. Relatively high CaO/Al2O3 and La/Zr and low Ti/Eu ratios from the lamprophyres and calculated melts in equilibrium with cumulus clinopyroxene point to a lithospheric mantle metasomatized by CO2-rich fluids, suggesting vein-plus-wall-rock melting mechanisms. The chemical differences among those liquids are thought to reflect both variable contributions of melting resulting from veins and variable clinopyroxene/garnet proportions of the source.
Abstract: The Pilanesberg Complex (South Africa) is one of the world's largest but least studied alkaline complexes. It consists of trachytes, phonolites, syenites and nepheline syenites (foyaites) and the preservation of the volcanic carapace makes it unique among the larger alkaline complexes. The intrusive history of the Pilanesberg Complex shows similarities to the Greenland Kangerlussuaq Intrusion, and our new whole-rock major and trace element analyses, combined with existing data, show that the complex belongs to the Sr-rich type of evolved alkaline rocks, more similar to the complexes of the Kola Peninsula than Ilímaussaq. Despite the absence of mafic lithologies, comparison with experimental studies shows that the parental magma was most likely an alkali basalt. Significant iron enrichment is caused by an early stage of fractionation involving clinopyroxene and amphibole rather than olivine and plagioclase, reflecting water-rich compositions and intermediate levels of oxygen fugacity. This fractionation trend has led to strong enrichment in Sr and Ba, but only moderate levels of Y and middle to heavy rare earth elements, and minimal Eu-anomaly. Late-stage water-rich fluids caused significant autometasomatism in most units. New U-Pb dating of titanite constrains the age of the Pilanesberg Complex as 1395 + 10/? 11 Ma. Initial 87Sr/86Sr isotope ratios around 0.7028 (?Sr1395 = ? 1) are typical for a moderately depleted mantle source, unlike the local lithospheric mantle. The combination of an enriched trace-element signature and depleted isotopic characteristics is evidence for small degrees of partial melting. Epsilon Sr values are similar to those reported for other alkaline complexes worldwide, emplaced in crust with contrasting geological histories; this likely reflects lithospheric metasomatism shortly before magmatism and minimal crustal contamination.
Russian Geology and Geophysics, Vol. 58, pp. 659-673.
Russia, Siberia
alkaline - Maimecha
Abstract: Comparative analysis of ultramafic meymechites of the Maimecha Suite and alkaline volcanics of the Ary-Dzhang Suite (foidites (nephelinites, analcimites, limburgites, etc.) and melilitites) has shown their consanguinity, which indicates their relationship with the same magmatic system periodically producing large amounts of alkaline ultramafic melts. We have studied the petrogeochemical and mineralogical compositions of rocks and melt inclusions in the hosted olivines. The rocks of the Maimecha and Ary-Dzhang Suite differ considerably in MgO content, which is well explained by the accumulation of olivine. The inclusions in olivines from the meymechites and the rocks of the Ary-Dzhang Suite correspond in composition to foidites. The trace and rare-earth element patterns are similar both in the foidites and meymechites and in the melt inclusions: They show negative anomalies of Rb and K and positive anomalies of Nb and Ta. The ratios of indicator elements (Nb/Ta, Ba/La, Ta/La, etc.) in the rocks of the Maimecha and Ary-Dzhang Suite are constant and almost independent of their Mg# values. The La/Yb ratio in the foidites is significantly higher than that in the meymechites and in the melt inclusions from their olivines, which indicates that the rocks of the Ary-Dzhang Suite resulted from the fractionation of highly magnesian alkaline picritoid melt.
Cal-alkaline mica-lamprophyres and F-Sn rhyolite intrusions associated F-Sn explosive breccia pipes and their relationship to Sn- polymetallic mineralization.
Abstract: The Pilanesberg Alkaline Complex (South Africa) consists of a partially eroded phonolitic-trachytic package of lavas and tuffs, intruded by consanguinous syenites and nepheline syenites (foyaites). The latter have been divided in several units, based on their colour and mineralogy. Most of the foyaitic units are sodic in composition, but whole rock analyses show that some samples are more potassic, with Na2O/K2O<0.8. This observation, together with old reports of leucite-bearing lavas [1], could suggest the existence of a second, potassic magmatic lineage. To investigate whether the observed potassium-enrichment is a primary feature, or the result of deuteric alteration, the mineralogical distinction between sodic and potassic samples was investigated. The mineralogy of the sodic samples is dominated by nepheline, alkali-feldspar and aegirine, ± titanite, amphibole, biotite, and late agpaitic phases [2]. Within the potassic samples, the main primary ferromagnesian mineral is biotite, which shows conspicuous zoning in thin section; nepheline has been extensively replaced by sodalite and cancrinite, but alkali-feldspar appears relatively unaltered. No agpaitic minerals were observed. U-Pb isotope systematics of titanite are similar for sodic and potassic samples in terms of the age (ca. 1.4 Ga) and composion of common Pb; Ar-Ar dating of biotite also gives ca. 1.4 Ga, showing that biotite is a primary magmatic phase. Compositions of the biotite in sodic and potassic samples are similar, with the sodic samples having slightly higher Fe# (independent of whole rock Fe#), higher Na, but lower (Na+K) and Ba. Zoning in biotite from potassic samples is related to a decrease in Mg, Ti and F in the rim of the crystals. Despite the primary character of the biotite, the question whether the potassic samples reflect a combination of alteration and perhaps minor crustal contamination, or a separate mag
Abstract: The rocks, which are totally comprised of olivine and mica, have been found among the xenoliths of the Udachnaya-East pipe (Yakutia). The essential amount (first percents) of ilmenite of different morphology has been found in two rocks. These exotic olivine glimmerites appeared to be similar to the polymict breccia in the wide variations of olivine (LUV709/11 and LUV659/11 - Mg#(%): 86-93 and 83-91, respectively), phlogopite ((wt.%), LUV659/11: SiO2 38.5-40.6, TiO2 2.5-6, Al2O3 11.3-14, Cr2O3 0.4-1, MgO 19.8-23.1, FeO 6.1-7.9, Na2O 0.5-1.3, K2O 8.6-9.9), ilmenite (LUV709/11: Mg#(%) 23.6-47.8; Cr2O3 (wt.%): 0.63-1.01) compositions and also in the abundance of accessory minerals (chromite, rutile, sulphides, calcite, dolomite, siderite, barite). The compositions of rock-forming minerals of the glimmerites do not fall within the compositional fields of similar minerals from the peridotites of kimberlite xenoliths but strongly overlap with that from the polymict breccias. Moreover, the compositions of phlogopite from the glimmerites have demonstrated similar in Al, Fe and Ti composition kimberlite trend typical of phlogopites from the polymict breccia of the South Africa. Unusual olivine glimmerites LUV659/11 and LUV709/11 were probably formed from the ancient protokimberlite melts like polymict breccias. Initially they have been strongly depleted and hence olivine is the main rock-forming mineral. Therefore, two main stages of metasomatic retreatment before the capture by kimberlite can be recognized. One is related with Ti and Fe introduction (ilmenite formation), another, more strong, with abundant introduction of Al and alkalis (mainly K) with a consequent formation of abundant phlogopite. These stages probably had several phases as evidenced by the compositional variations of the formed minerals.
Balasubramani, S., Sahoo, P., Bhattacharya, D., Rengarajan, M., Thangavel, S., Bhatt, A.K., Verma, M.B., Nanda, L.K.
A note on anomalous concentration of scandium in the Pakkanadu alkaline complex, Salem District, Tamil Nadu, India.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 46.
India
alkaline rocks
Abstract: Pakkanadu Alkaline complex (PAC) of Neoproterozoic age is located at the southwestern end of Dharmapuri rift/shear zone on the northern part of southern granulitic terrain in Tamil Nadu, India. PAC mainly comprises carbonatite-syenitepyroxenite suite of rocks. Syenite is the predominant rock exposed on the eastern and western part of the explored area with enclaves of pyroxenite and dunite. The carbonatite (sovite) occurs as thin veins/bands and discontinuous lenticular bodies intrusive into highly deformed biotite schist that is considered as the fenitised product of pyroxenite traceable over a strike length of 1.5 km. Petromineralogical study of the biotite schist, pyroxenite containing carbonatite rock and carbonatite indicated presence of monazite, allanite, sphene and betafite as the main radioactive minerals occurring as inclusion within biotite or as discrete mineral grains. Other ore minerals are apatite, thorite, titanite, rutile and barite. Chloritisation, hematitisation, silicification and calcitisation are the main wall rock alteration observed in pyroxenite and syenite. Sub-surface exploration carried out by Atomic Minerals Directorate (AMD) in PAC revealed that biotite schist (n=166) contains anomalously high concentration of Scandium (11-1275 ppm, av.161 ppm), REE (67-58275 ppm, av. 14836 ppm,) and V (5-620 ppm, av. 127 ppm, with carbonatite veins and syenite (n=149) contain scandium (10-462 ppm, av.71 ppm,), REE (18-57510 ppm, av. 4106 ppm) and V (1-285 ppm, av. 48 ppm). In these rocks, LREE (12.5-57670 ppm, av. 9617 ppm, n=315) shows enrichment over HREE (7.1-774 ppm, av. 173 ppm, n=315). The concentration of Scandium (Av. 166 and 71 ppm in biotite schist and syenite respectively) is anomalous as compared to its crustal abundance (22 ppm). Geochemical analyses of the rock indicate that the radioactive biotite schist, pyroxenite containing carbonatite veins generally shows higher Sc and REE concentrations as compared to those of the other rocks (syenite). However, there is no significant correlation between REE and Sc. The higher concentration of scandium in PAC is possibly due to selective partitioning of it into minerals like apatite, pyrochlore, allanite, monazite and other REE bearing phases, apart from its concentration in the ferromagnesian minerals. Scandium rarely concentrates in nature as independent ore mineral. The demand for the metal is very high due to multiple high value commercial uses as an alloy with aluminum, specifically in aerospace and automobile industry, besides, in solid oxide fuel cells (SOFC) in electrical industries. Eight boreholes drilled as part of the preliminary subsurface exploration in PAC, covering an area of 0.05 sq. km, indicated an elevated Scandium content of about 6 times that of the average crustal abundance.
Gautam, I., Bhutani, R., Balakrishnan, S., Chatterjee, A., George, B.G., Ray, J.S.
142Nd/144Nd of alkaline magmas in Phenai Mat a complex, Chhota Udaipur, Deccan flood basalt province.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 14.
India
alkaline rocks
Abstract: The 65 million year old alkaline plug at Phenai Mata Complex, in Chota Udaipur sub province, is often linked to the last pulse of the Deccan volcanism. However, many believe that the Deccan-Reunion mantle plume that was responsible for the generation of flood basalts might not have been the source of Phenai Mata. It, however, could have acted as a heat source for these magmas derived from the subcontinentallithospheric- mantle (SCLM). Since the SCLM is generally considered to be a nonconvective mantle domain it has the potential to preserve some of the geochemical evidence of the early silicate Earth differentiation, e.g., 142Nd anomaly. In search of such signatures we analysed alkali basalts from the complex for their 142Nd/144Nd using high precision thermal ionization mass spectrometry. Whereas the geochemical characterization of these samples confirmed the lithospheric origin of their source magmas, their ? 142Nd compositions are found to be normal with respect to terrestrial standards. We infer that either the mantle source of Phenai Mata does not represent a true non-convective mantle or it is too young to retain any evidence of 146Sm decay.
Journal of the Geological Society of India, Vol. 91, 2, pp. 135-146.
India
Prakasam alkaline province
Abstract: Three distinct alkaline magmas, represented by shonkinite, lamprophyre and alkali basalt dykes, characterize a significant magmatic expression of rift-related mantle-derived igneous activity in the Mesoproterozoic Prakasam Alkaline Province, SE India. In the present study we have estimated emplacement velocities (ascent rates) for these three varied alkaline magmas and compared with other silicate magmas to explore composition control on the ascent rates. The alkaline dykes have variable widths and lengths with none of the dykes wider than 1 m. The shonkinites are fine- to medium-grained rocks with clinopyroxene, phologopite, amphibole, K-feldspar perthite and nepheline as essential minerals. They exhibit equigranular hypidiomorphic to foliated textures. Lamprophyres and alkali basalts characteristically show porphyritic textures. Olivine, clinopyroxene, amphibole and biotite are distinct phenocrysts in lamprophyres whereas olivine, clinopyroxene and plagioclase form the phenocrystic mineralogy in the alkali basalts. The calculated densities [2.54-2.71 g/cc for shonkinite; 2.61-2.78 g/cc for lamprophyre; 2.66-2.74 g/cc for alkali basalt] and viscosities [3.11-3.39 Pa s for shonkinite; 3.01-3.28 Pa s for lamprophyre; 2.72-3.09 Pa s for alkali basalt] are utilized to compute velocities (ascent rates) of the three alkaline magmas. Since the lamprophyres and alkali basalts are crystal-laden, we have also calculated effective viscosities to infer crystal control on the velocities. Twenty percent of crystals in the magma increase the viscosity by 2.7 times consequently decrease ascent rate by 2.7 times compared to the crystal-free magmas. The computed ascent rates range from 0.11-2.13 m/sec, 0.23-2.77 m/sec and 1.16-2.89 m/sec for shonkinite, lamprophyre and alkali basalt magmas respectively. Ascent rates increase with the width of the dykes and density difference, and decrease with magma viscosity and proportion of crystals. If a constant width of 1 m is assumed in the magma-filled dyke propagation model, then the sequence of emplacement velocities in the decreasing order is alkaline magmas (4.68-15.31 m/sec) > ultramafic-mafic magmas (3.81-4.30 m/sec) > intermediate-felsic magmas (1.76-2.56 m/sec). We propose that SiO2 content in the terrestrial magmas can be modeled as a semi-quantitative “geospeedometer” of the magma ascent rates.
Journal of the Geological Society of India, Vol. 91, pp. 135-146.
India
Alkaline - Prakasam
Abstract: Three distinct alkaline magmas, represented by shonkinite, lamprophyre and alkali basalt dykes, characterize a significant magmatic expression of rift-related mantle-derived igneous activity in the Mesoproterozoic Prakasam Alkaline Province, SE India. In the present study we have estimated emplacement velocities (ascent rates) for these three varied alkaline magmas and compared with other silicate magmas to explore composition control on the ascent rates. The alkaline dykes have variable widths and lengths with none of the dykes wider than 1 m. The shonkinites are fine- to medium-grained rocks with clinopyroxene, phologopite, amphibole, K-feldspar perthite and nepheline as essential minerals. They exhibit equigranular hypidiomorphic to foliated textures. Lamprophyres and alkali basalts characteristically show porphyritic textures. Olivine, clinopyroxene, amphibole and biotite are distinct phenocrysts in lamprophyres whereas olivine, clinopyroxene and plagioclase form the phenocrystic mineralogy in the alkali basalts. The calculated densities [2.54-2.71 g/cc for shonkinite; 2.61-2.78 g/cc for lamprophyre; 2.66-2.74 g/cc for alkali basalt] and viscosities [3.11-3.39 Pa s for shonkinite; 3.01-3.28 Pa s for lamprophyre; 2.72-3.09 Pa s for alkali basalt] are utilized to compute velocities (ascent rates) of the three alkaline magmas. Since the lamprophyres and alkali basalts are crystal-laden, we have also calculated effective viscosities to infer crystal control on the velocities. Twenty percent of crystals in the magma increase the viscosity by 2.7 times consequently decrease ascent rate by 2.7 times compared to the crystal-free magmas. The computed ascent rates range from 0.11-2.13 m/sec, 0.23-2.77 m/sec and 1.16-2.89 m/sec for shonkinite, lamprophyre and alkali basalt magmas respectively. Ascent rates increase with the width of the dykes and density difference, and decrease with magma viscosity and proportion of crystals. If a constant width of 1 m is assumed in the magma-filled dyke propagation model, then the sequence of emplacement velocities in the decreasing order is alkaline magmas (4.68-15.31 m/sec) > ultramafic-mafic magmas (3.81-4.30 m/sec) > intermediate-felsic magmas (1.76-2.56 m/sec). We propose that SiO2 content in the terrestrial magmas can be modeled as a semi-quantitative "geospeedometer" of the magma ascent rates.
Journal of the Geological Society of India, Vol. 91, pp. 395-399.
India
Alkaline - Mundwara
Abstract: The occurrence of a rare mantle-derived chrome-diopside megacryst (~8 mm), containing inclusions of olivine, in a lamprophyre dyke from the late Cretaceous polychronous (~100 - 68 Ma) Mundwara alkaline complex of NW India is reported. The olivine inclusions are forsteritic (Fo: 85.23) in composition, and their NiO (0.09 wt%) and CaO (0.13 wt%) contents imply derivation from a peridotitic mantle source. The composition of the chrome diopside (Cr2O3: 0.93 wt ) (Wo45.27 En48.47 Fs5.07 and Ac1.18) megacryst is comparable to that occurring in the garnet peridotite xenoliths found in diamondiferous kimberlites from Archaean cratons. Single pyroxene thermobarometry revealed that this chrome diopside megacryst was derived from a depth range of ~100 km, which is relatively much deeper than that of the chrome-diopside megacrysts (~40-50 km) reported in spinellherzolite xenoliths from the alkali basalts of Deccan age (ca. 66- 67 Ma) from the Kutch, NW India. This study highlights that pre- Deccan lithosphere, below the Mundwara alkaline complex, was at least ~100 km thick and, likely, similar in composition to that of the cratonic lithosphere.
Mineralogy and Petrology, doi.org/101007/ s00710-018-0623-6 10p.
Europe, Sweden
alkaline
Abstract: Potassic-richterite, ideally AKB(NaCa)CMg5TSi8O22W(OH)2, is recognized as a valid member of the amphibole supergroup (IMA-CNMNC 2017-102). Type material is from the Pajsberg Mn-Fe ore field, Filipstad, Värmland, Sweden, where the mineral occurs in a Mn-rich skarn, closely associated with mainly phlogopite, jacobsite and tephroite. The megascopic colour is straw yellow to grayish brown and the luster vitreous. The nearly anhedral crystals, up to 4 mm in length, are pale yellow (non-pleochroic) in thin section and optically biaxial (?), with ??=?1.615(5), ??=?1.625(5), ??=?1.635(5). The calculated density is 3.07 g•cm?1. VHN100 is in the range 610-946. Cleavage is perfect along {110}. EPMA analysis in combination with Mössbauer and infrared spectroscopy yields the empirical formula (K0.61Na0.30Pb0.02)?0.93(Na1.14Ca0.79Mn0.07)?2(Mg4.31Mn0.47Fe3+0.20)?5(Si7.95Al0.04Fe3+0.01)?8O22(OH1.82F0.18)?2 for a fragment used for collection of single-crystal X-ray diffraction data. The infra-red spectra show absorption bands at 3672 cm?1 and 3736 cm?1 for the ? direction. The crystal structure was refined in space group C2/m to R1?=?3.6% [I >?2?(I)], with resulting cell parameters a?=?9.9977(3) Å, b?=?18.0409(4) Å, c?=?5.2794(2) Å, ??=?104.465(4)°, V?=?922.05(5) Å3 and Z?=?2. The A and M(4) sites split into A(m) (K+), A(2/m) (Na+), A(2) (Pb2+), and M(4?) (Mn2+) subsites, respectively. The remaining Mn2+ is strongly ordered at the octahedrally coordinated M(2) site, possibly together with most of Fe3+. The skarn bearing potassic-richterite formed at peak metamorphism, under conditions of low SiO2 and Al2O3 activities and relatively high oxygen fugacities.
Physics and Chemistry of Minerals, Vol. 45, pp. 745-758.
Russia, Kola Peninsula
alkaline
Abstract: The new eudialyte-group mineral siudaite, ideally Na8(Mn2+2Na)Ca6Fe3+3Zr3NbSi25O74(OH)2Cl•5H2O, was discovered in a peralkaline pegmatite situated at the Eveslogchorr Mt., Khibiny alkaline massif, Kola Peninsula, Russia. The associated minerals are aegirine, albite, microcline, nepheline, astrophyllite, and loparite-(Ce). Siudaite forms yellow to brownish-yellow equant anhedral grains up to 1.5 cm across. Its lustre is vitreous, and the streak is white. Cleavage is none observed. The Mohs’ hardness is 4½. Density measured by hydrostatic weighing is 2.96(1) g/cm3. Density calculated using the empirical formula is equal to 2.973 g/cm3. Siudaite is nonpleochroic, optically uniaxial, negative, with ??=?1.635(1) and ??=?1.626(1) (??=?589 nm). The IR spectrum is given. The chemical composition of siudaite is (wt%; electron microprobe, H2O determined by HCN analysis): Na2O 8.40, K2O 0.62, CaO 9.81, La2O3 1.03, Ce2O3 1.62, Pr2O3 0.21, Nd2O3 0.29, MnO 6.45, Fe2O3 4.51. TiO2 0.54, ZrO2 11.67, HfO2 0.29, Nb2O5 2.76, SiO2 47.20, Cl 0.54, H2O 3.5, -O?=?Cl ??0.12, total 99.32. According to Mössbauer spectroscopy data, all iron is trivalent. The empirical formula (based on 24.5 Si atoms pfu, in accordance with structural data) is [Na7.57(H2O)1.43]?9(Mn1.11Na0.88Ce0.31La0.20Nd0.05Pr0.04K0.41)?3(H2O)1.8(C a5.46Mn0.54)?6(Fe3+1.76Mn2+1.19)?2.95Nb0.65(T i0.20Si0.50)?0.71(Zr2.95Hf0.04Ti0.01)?3Si24.00Cl0.47O70(OH)2Cl0.47•1.2H2O. The crystal structure was determined using single-crystal X-ray diffraction data. The new mineral is trigonal, space group R3m, with a?=?14.1885(26) Å, c?=?29.831(7) Å, V?=?5200.8(23) Å3 and Z?=?3. Siudaite is chemically related to georgbarsanovite and is its analogue with Fe3+-dominant M2 site. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 6.38 (60) (-114), 4.29 (55) (-225), 3.389 (47) (131), 3.191 (63) (-228). 2.963 (100) (4-15), 2.843 (99) (-444), 2.577 (49) (3-39). Siudaite is named after the Polish mineralogist and geochemist Rafa? Siuda (b. 1975).
Abstract: Low-volume alkaline silicate and carbonate magmas are products of volatile-controlled incipient melting processes in the Earth’s mantle. Although this form of melting is ubiquitous beneath the thick and cold portions of continental lithosphere, such melts rarely reach the Earth’s surface due to a combination of their small volumes, reactive nature, and great depths of origin. In spite of being rare at surface, the impact of alkaline and carbonate magmatism on the dynamic stability of mantle lithosphere and its metal endowment may be disproportionately large, but it is difficult to grasp in the absence of spatial and temporal constraints on melt mobility. We review evidence from major alkaline and carbonatite provinces for metasomatic overprinting of the underlying continental mantle lithosphere, and evaluate how these processes influenced plate tectonic evolution in these regions. Key examples from Greenland and Africa show that metasomatic weakening of mantle lithosphere by pervasive alkaline and carbonate melts is frequently the first step in continent fragmentation ultimately leading to supercontinent dispersal. A major obstacle in identifying carbonate melt metasomatized mantle is the use of differentiated ‘surface’ carbonatite compositions as proxies for geochemical processes operating at great depths. We assess the robustness of some of the classic geochemical proxies, such as Ti/Eu and Zr/Sm, and identify new promising fingerprints of passing carbonate melts in the deep mantle lithosphere. New evidence from the Kaapvaal craton, one of world’s best endowed metallogenic provinces, shows that redox- and volatile-controlled alkaline melting events can effectively mobilize sulphide-hosted PGE and base metal budgets from eclogite components within the thick mantle lithosphere. Such precursor alkaline magmatic events, heralding the formation of major continental rifts and mantle plume impingement, can enhance the metal contents of subsequent asthenosphere-derived mafic magmas, thereby upgrading oreforming potential. However, economic metal deposits only form when geologic conditions during magma emplacement in the crust are favorable, with mantle metal budgets being less critical.
South African Journal of Geology, Vol. 122, 4, pp. 397-420.
India
alkaline, carbonatites
Abstract:
On the last page of his 1937 book “Our Wandering Continents” Alex Du Toit advised the geological community to develop the field of “comparative geology”, which he defined as “the study of continental fragments”. This is precisely the theme of this paper, which outlines my research activities for the past 28 years, on the continental fragments of the Indian Ocean. In the early 1990s, my colleagues and I were working in Madagascar, and we recognized the need to appreciate the excellent geological mapping (pioneered in the 1950s by Henri Besairie) in a more modern geodynamic context, by applying new ideas and analytical techniques, to a large and understudied piece of continental crust. One result of this work was the identification of a 700 to 800 Ma belt of plutons and volcanic equivalents, about 450 km long, which we suggested might represent an Andean-type arc, produced by Neoproterozoic subduction. We wondered if similar examples of this magmatic belt might be present elsewhere, and we began working in the Seychelles, where late Precambrian granites are exposed on about 40 of the >100 islands in the archipelago. Based on our new petrological, geochemical and geochronological measurements, we built a case that these ~750 Ma rocks also represent an Andean-type arc, coeval with and equivalent to the one present in Madagascar. By using similar types of approaches, we tracked this arc even further, into the Malani Igneous Province of Rajasthan, in northwest India. Our paleomagnetic data place these three entities adjacent to each other at ~750 Ma, and were positioned at the margins, rather than in the central parts of the Rodinia supercontinent, further supporting their formation in a subduction-related continental arc. A widespread view is that in the Neoproterozoic, Rodinia began to break apart, and the more familiar Gondwana supercontinent was assembled by Pan-African (~500 to 600 Ma) continental collisions, marked by the highly deformed and metamorphosed rocks of the East African Orogen. It was my mentor, Kevin Burke, who suggested that the present-day locations of Alkaline Rocks and Carbonatites (called “ARCs”) and their Deformed equivalents (called “DARCs”), might mark the outlines of two well-defined parts of the Wilson cycle. We can be confident that ARCs formed originally in intracontinental rift settings, and we postulated that DARCs represent suture zones, where vanished oceans have closed. We also found that the isotopic record of these events can be preserved in DARC minerals. In a nepheline syenite gneiss from Malawi, the U-Pb age of zircons is 730 Ma (marking the rifting of Rodinia), and that of monazites is 522 Ma (marking the collisional construction of Gondwana). A general outline of how and when Gondwana broke apart into the current configuration of continental entities, starting at about 165 Ma, has been known for some time, because this record is preserved in the magnetic properties of ocean-floor basalts, which can be precisely dated. A current topic of active research is the role that deep mantle plumes may have played in initiating, or assisting, continental fragmentation. I am part of a group of colleagues and students who are applying complementary datasets to understand how the Karoo (182 Ma), Etendeka (132 Ma), Marion (90 Ma) and Réunion (65 Ma) plumes influenced the break-up of Gondwana and the development of the Indian Ocean. Shortly after the impingement of the Karoo plume at 182 Ma, Gondwana fragmentation began as Madagascar + India + Antarctica separated from Africa, and drifted southward. Only after 90 Ma, when Madagascar was blanketed by lavas of the Marion plume, did India begin to rift, and rapidly drifted northward, assisted by the Marion and Deccan (65 Ma) plumes, eventually colliding with Asia to produce the Himalayas. It is interesting that a record of these plate kinematics is preserved in the large Permian - Eocene sedimentary basins of western Madagascar: transtensional pull-apart structures are dextral in Jurassic rocks (recording initial southward drift with respect to Africa), but change to sinistral in the Eocene, recording India’s northward drift. Our latest work has begun to reveal that small continental fragments are present in unexpected places. In the young (max. 9 Ma) plume-related, volcanic island of Mauritius, we found Precambrian zircons with ages between 660 and 3000 Ma, in beach sands and trachytic lavas. This can only mean that a fragment of ancient continent must exist beneath the young volcanoes there, and that the old zircons were picked up by ascending magmas on their way to surface eruption sites. We speculate, based on gravity inversion modelling, that continental fragments may also be present beneath the Nazareth, Saya de Malha and Chagos Banks, as well as the Maldives and Laccadives. These were once joined together in a microcontinent we called "Mauritia", and became scattered across the Indian Ocean during Gondwana break-up, probably by mid-ocean ridge "jumps". This work, widely reported in international news media, allows a more refined reconstruction of Gondwana, suggests that continental break-up is far more complex than previously perceived, and has important implications for regional geological correlations and exploration models. Our results, as interesting as they may be, are merely follow-ups that build upon the prescient and pioneering ideas of Alex Du Toit, whose legacy I appreciatively acknowledge.
Abstract: To provide new insights into the origin and evolution of ultramafic lamprophyres (UMLs) and their mantle source, we examined two UML (aillikite and damtjernite) occurrences of different ages in the western portion of the Siberian Craton (Ilbokich and Chadobets). New age, mineral and rock geochemistry, along with Sr-Nd-Pb-C-O isotope data was obtained. Our new 206Pb/238U perovskite age (399 ± 4 Ma) confirms the previously published Early Devonian age of the Ilbokich aillikite. RbSr isochron and 40Ar/39Ar dating yielded a Middle Triassic age (243 ± 3 Ma and 241 ± 1 Ma, respectively) for the Chadobets aillikites, indicating post-Trap emplacement of these rocks. Both UMLs are characterized by incompatible elements, including light rare earth element (LREE) enrichments (La is up to ×200 chondrite concentration), and strong fractionation of REEs ((La/Yb)n: 33-84). Despite the close geochemical affinity of both UMLs, the Nd isotopic compositions of aillikites, as well as the Pb isotopic composition of Chadobets and Ilbokich UMLs, do not overlap and are distinctly different from each other. The initial Sr and Nd isotopic compositions of the Ilbokich UMLs fall in within a narrow 87Sr/86Sr0 range (0.7032-0.7042) and ?Nd(T) (4.03-3.97). Chadobets UMLs have a similar Sr isotopic signature (87Sr/86Sr0: 0.7031-0.7043) and a more depleted Nd isotopic signature (?Nd(T) 4.09-5.08). The initial Pb isotope compositions of the Chadobets UMLs are moderately radiogenic, ranging between 206Pb/204Pb = 18.4-19.0, 208Pb/204Pb = 38.3-38.8, and are characterized by a narrow 207Pb/204Pb ratio between 15.5 and 15.6. The Ilbokich Pb isotope compositions are less variable and range between 206Pb/204Pb = 18.0-18.4, 208Pb/204Pb = 37.8-38.4 and 207Pb/204Pb ratios between 15.5 and 15.6. The oxygen isotopic composition of carbonate from both UMLs is characterized by highly variable ?18O values from +12.1 and up to +20.5‰ (SMOW). The isotopic composition of ?13C values range from ?1.3‰ to ?7.1. Based on the minor impact of crustal contamination in both aillikites, it is inferred that their radiogenic isotope composition reflects a mantle source signature. The mantle source of the Chadobets aillikites is likely to include carbonatitic magma as a metasomatic agent. In contrast, phlogopite-rich metasomes within the lithospheric mantle could have contributed more significantly to the Ilbokich aillikites. These metasomes could be formed during the Caledonian orogeny, which did not only affect the southwestern boundary of the Siberian Craton, but also expanded to the craton interior. This study provides additional support for the evolution of the south-western portion of the Siberian SCLM, ranging from mantle containing phlogopite enrichment domains during the Early Devonian to hydrous-phase reduced mantle in the Triassic due to the thermal impact of the Siberian Traps.
Abstract: To provide new insights into the origin and evolution of ultramafic lamprophyres (UMLs) and their mantle source, we examined two UML (aillikite and damtjernite) occurrences of different ages in the western portion of the Siberian Craton (Ilbokich and Chadobets). New age, mineral and rock geochemistry, along with Sr-Nd-Pb-C-O isotope data was obtained. Our new 206Pb/238U perovskite age (399 ± 4 Ma) confirms the previously published Early Devonian age of the Ilbokich aillikite. RbSr isochron and 40Ar/39Ar dating yielded a Middle Triassic age (243 ± 3 Ma and 241 ± 1 Ma, respectively) for the Chadobets aillikites, indicating post-Trap emplacement of these rocks. Both UMLs are characterized by incompatible elements, including light rare earth element (LREE) enrichments (La is up to ×200 chondrite concentration), and strong fractionation of REEs ((La/Yb)n: 33-84). Despite the close geochemical affinity of both UMLs, the Nd isotopic compositions of aillikites, as well as the Pb isotopic composition of Chadobets and Ilbokich UMLs, do not overlap and are distinctly different from each other. The initial Sr and Nd isotopic compositions of the Ilbokich UMLs fall in within a narrow 87Sr/86Sr0 range (0.7032-0.7042) and ?Nd(T) (4.03-3.97). Chadobets UMLs have a similar Sr isotopic signature (87Sr/86Sr0: 0.7031-0.7043) and a more depleted Nd isotopic signature (?Nd(T) 4.09-5.08). The initial Pb isotope compositions of the Chadobets UMLs are moderately radiogenic, ranging between 206Pb/204Pb = 18.4-19.0, 208Pb/204Pb = 38.3-38.8, and are characterized by a narrow 207Pb/204Pb ratio between 15.5 and 15.6. The Ilbokich Pb isotope compositions are less variable and range between 206Pb/204Pb = 18.0-18.4, 208Pb/204Pb = 37.8-38.4 and 207Pb/204Pb ratios between 15.5 and 15.6. The oxygen isotopic composition of carbonate from both UMLs is characterized by highly variable ?18O values from +12.1 and up to +20.5‰ (SMOW). The isotopic composition of ?13C values range from ?1.3‰ to ?7.1. Based on the minor impact of crustal contamination in both aillikites, it is inferred that their radiogenic isotope composition reflects a mantle source signature. The mantle source of the Chadobets aillikites is likely to include carbonatitic magma as a metasomatic agent. In contrast, phlogopite-rich metasomes within the lithospheric mantle could have contributed more significantly to the Ilbokich aillikites. These metasomes could be formed during the Caledonian orogeny, which did not only affect the southwestern boundary of the Siberian Craton, but also expanded to the craton interior. This study provides additional support for the evolution of the south-western portion of the Siberian SCLM, ranging from mantle containing phlogopite enrichment domains during the Early Devonian to hydrous-phase reduced mantle in the Triassic due to the thermal impact of the Siberian Traps.
Abstract: The redox state of Earth’s upper mantle in several tectonic settings, such as cratonic mantle, oceanic mantle, and mantle wedges beneath magmatic arcs, has been well documented. In contrast, oxygen fugacity (graphic) data of upper mantle under orogens worldwide are rare, and the mechanism responsible for the mantle graphic condition under orogens is not well constrained. In this study, we investigated the graphic of mantle xenoliths derived from the southern Tibetan lithospheric mantle beneath the Himalayan orogen, and that of postcollisional ultrapotassic volcanic rocks hosting the xenoliths. The graphic of mantle xenoliths ranges from ?FMQ = +0.5 to +1.2 (where ?FMQ is the deviation of log graphic from the fayalite-magnetite-quartz buffer), indicating that the southern Tibetan lithospheric mantle is more oxidized than cratonic and oceanic mantle, and it falls within the typical range of mantle wedge graphic values. Mineralogical evidence suggests that water-rich fluids and sediment melts liberated from both the subducting Neo-Tethyan oceanic slab and perhaps the Indian continental plate could have oxidized the southern Tibetan lithospheric mantle. The graphic conditions of ultrapotassic magmas show a shift toward more oxidized conditions during ascent (from ?FMQ = +0.8 to +3.0). Crustal evolution processes (e.g., fractionation) could influence magmatic graphic, and thus the redox state of mantle-derived magma may not simply represent its mantle source.
Kara, J., Vaisanen, M., Heinonen, J.S., Lahaye, Y., O'Brien, H., Huhma, H.
Tracing arcologites in the Paleoproteroic era - a shift from 1.88 Ga calc-alkaline to 1.86 Ga high-Nb and adakite-like magmatism in central Fennoscandian shield.
Abstract: In the last few decades, advanced monitoring networks have been extended to the main active volcanoes, providing warnings for variations in volcano dynamics. However, one of the main tasks of modern volcanology is the correct interpretation of surface-monitored signals in terms of magma transfer through the Earth's crust. In this frame, it is crucial to investigate decompression-induced magma degassing as it controls magma ascent towards the surface and, in case of eruption, the eruptive style and the atmospheric dispersal of tephra and gases. Understanding the degassing behaviour is particularly intriguing in the case of poorly explored evolved alkaline magmas. In fact, these melts frequently feed hazardous, highly explosive volcanoes (e.g., Campi Flegrei, Somma-Vesuvius, Colli Albani, Tambora, Azores and Canary Islands), despite their low viscosity that usually promotes effusive and/or weakly explosive eruptions. Decompression experiments, together with numerical models, are powerful tools to examine magma degassing behaviour and constrain field observations from natural eruptive products and monitoring signals. These approaches have been recently applied to evolved alkaline melts, yet numerous open questions remain. To cast new light on the degassing dynamics of evolved alkaline magmas, in this study we present new results from decompression experiments, as well as a critical review of previous experimental works. We achieved a comprehensive dataset of key petrological parameters (i.e., 3D textural data for bubbles and microlites using X-ray computed microtomography, glass volatile contents and nanolite occurrence) from experimental samples obtained through high temperature-high pressure isothermal decompression experiments on trachytic alkaline melts at super-liquidus temperature. We explored systematically a range of final pressures (from 200 to 25 MPa), decompression rates (from 0.01 to 1 MPa s?1), and volatile (H2O and CO2) contents. On these grounds, we integrated coherently literature data from decompression experiments on evolved alkaline (trachytic and phonolitic) melts under various conditions, with the aim to fully constrain the degassing mechanisms and timescales in these magmas. Finally, we simulated numerically the experimental conditions to evaluate strengths and weaknesses in decrypting degassing behaviour from field observations. Our results highlight that bubble formation in evolved alkaline melts is primarily controlled by the initial volatile (H2O and CO2) content during magma storage. In these melts, bubble nucleation needs low supersaturation pressures (? 50-112 MPa for homogeneous nucleation, ? 13-25 MPa for heterogeneous nucleation), resulting in high bubble number density (~ 1012-1016 m?3), efficient volatile exsolution and thus in severe rheological changes. Moreover, the bubble number density is amplified in CO2-rich melts (mole fraction XCO2 ? 0.5), in which continuous bubble nucleation predominates on growth. These conditions typically lead to highly explosive eruptions. However, moving towards slower decompression rates (? 10?1 MPa s?1) and H2O-rich melts, permeable outgassing and inertial fragmentation occur, promoting weakly explosive eruptions. Finally, our findings suggest that the exhaustion of CO2 at deep levels, and the consequent transition to a H2O-dominated degassing, can crucially enhance magma vesiculation and ascent. In a hazard perspective, these constraints allow to postulate that time-depth variations of unrest signals could be significantly weaker/shorter (e.g., minor gas emissions and short-term seismicity) during major eruptions than in small-scale events.
South African Journal of Geology, Vol. 123, 4, pp. 597-614. pdf
Africa, South Africa
alkaline rocks
Abstract: Numerous Mesoproterozoic alkaline intrusions belonging to the Pilanesberg Alkaline Province are present within the Transvaal sub-basin of the Kaapvaal Craton. The Pilanesberg Complex is the best-known example; it represents one of the world’s largest alkaline complexes, and is associated with a northwest-southeast trending dyke swarm that extends from Botswana to the southwest of Johannesburg. This paper documents the results of a petrological and geochemical study of a thin mafic sill (here referred to as an alkaline igneous body, AIB), which intrudes the ca. 2 200 Ma Silverton Formation close to the southernmost part of the Pilanesberg dyke swarm. The AIB has only been observed in cores from a borehole drilled close to Carletonville. It is hypocrystalline, containing randomly oriented elongated skeletal kaersutite crystals and 6 to 8 mm varioles mainly composed of radially oriented acicular plagioclase. These two textures are related to undercooling, probably linked to the limited thickness (70 cm) of the AIB coupled with a probable shallow emplacement depth. Ar-Ar dating of the kaersutite gives an age of ca. 1 400 Ma, similar to the age of Pilanesberg Complex. However, the AIB is an alkaline basaltic andesite and is thus notably less differentiated than the Pilanesberg Complex and some of its associated dykes, such as the Maanhaarrand dyke, for which we provide whole-rock geochemical data. Literature data indicate that the Pilanesberg dyke swarm also contains mafic hypabyssal rocks suggesting a link between the dyke swarm and the AIB. The AIB is characterized by strongly negative ?Nd and ?Hf, that cannot be related to crustal contamination, as shown by positive Ti and P anomalies, and the absence of negative Nb-Ta anomalies in mantle-normalised trace element diagrams. The AIB magma is interpreted to have been derived from a long-lived enriched, probably lithospheric mantle reservoir. The AIB thus provides important information on the magma source of the Pilanesberg Alkaline Province.
Geologica Carpathica ** Eng, Vol. 71, 4, pp. 343-360. pdf
Europe, Czech Republic
alkaline rocks
Abstract: Sills of hydrothermally altered alkaline magmatic rock (teschenite) of Lower Cretaceous age at the ?er?ák and ?epišt? sites in the Silesian Unit (Flysch Belt of the Outer Western Carpathians, Czech Republic) host leucocratic dykes and nests which contain accessory minerals enriched in Zr, Nb and REE: Zr-, Nb-rich titanite, zircon, gittinsite, pyrochlore, monazite, REE-rich apatite, epidote, and vesuvianite. Titanite forms wedge-shaped crystals or irregular aggregates enclosed in the analcime groundmass or overgrowths on Zr-rich ferropargasite and taramite or Zr-rich aegirine-augite to aegirine. Titanite crystals show oscillatory or irregular patchy to sector zoning and contain up to 17.7 wt. % ZrO2 and 19.6 wt. % Nb2O5, and ?1.1 wt. % REE2O3. High-field-strength elements (HFSE) are incorporated into the structure of the studied titanite predominantly by substitutions: (i) [6]Ti4+???[6]Zr4+; (ii) [6]Ti4+?+?[6]Al3+???[6]Zr4+?+?[6]Fe3+; and (iii) [6]2Ti4+???[6]Nb5+?+?[6](Al, Fe)3+. Magmatic fractional crystallization, high-temperature hydrothermal autometasomatic overprint and low-temperature hydrothermal alterations resulted in the formation of the HFSE-rich mineral assemblages within the leucocratic teschenites. Autometamorphic processes caused by high-temperature hypersaline aqueous solutions (salinity ~50 wt. %, ~390-510 °C), which were released from the HFSE-enriched residual melt, played a major role in the crystallization of Zr-, Nb-, and REE-rich minerals. The mobilization of HFSE could have occurred either by their sequestration into a fluid phase exsolved from the crystallizing melt or by superimposed alteration processes. The distinctive positive Eu anomaly (EuCN/Eu*?=?1.85) of leucocratic dykes infers possible mixing of Eu2+-bearing magmatic fluids with more oxidized fluids.
Geologica Carpathica ** Eng, Vol. 65, 6, pp. 419-431. pdf doi: 10.15 /geoca-2015-0003
Europe, Czech Republic
alkaline rocks
Abstract: Hydrothermal mineralization hosted by the Lower Cretaceous igneous rock of the teschenite association at Jasenice (Silesian Unit, Flysch Belt, Outer Western Carpathians) occurs in two morphological types - irregular vein filled by granular calcite and regular composite vein formed by both fibrous and granular calcite and minor chlorite, quartz, and pyrite. Crosscutting evidence indicates that the granular veins are younger than the composite vein. The composite vein was formed by two mechanisms at different times. The arrangement of solid inclusions in the marginal fibrous zone suggests an episodic growth by the crack-seal mechanism during syntectonic deformation which was at least partially driven by tectonic suction pump during some stages of the Alpine Orogeny. Both the central part of the composite vein and monomineral veins developed in a brittle regime. In these cases, the textures of vein suggest the flow of fluids along an open fracture. The parent fluids of both types of vein are characterized by low temperatures (Th=66-163 °C), low salinities (0.4 to 3.4 wt. % NaCl eq.), low content of strong REE-complexing ligands, and ?18O and ?13C ranges of + 0.2/+12.5 %. SMOW and -11.8/-14.1 %. PDB, respectively. The parent fluids are interpreted as the results of mixing of residual seawater and diagenetic waters produced by dewatering of clay minerals in the associ-ated flysch sediments. The flow of fluids was controlled by tectonic deformation of the host rock.
Nature Scientific Reports, doi.org/10.1038/ s41598-020-76800-0 10p. Pdf
Australia, Africa, South Africa
alkaline magmatism
Abstract: Large-scale mantle convective processes are commonly reflected in the emplacement of Large Igneous Provinces (LIPs). These are high-volume, short-duration magmatic events consisting mainly of extensive flood basalts and their associated plumbing systems. One of the most voluminous LIPs in the geological record is the ~?2.06 billion-year-old Bushveld Igneous Complex of South Africa (BIC), one of the most mineralised magmatic complexes on Earth. Surprisingly, the known geographic envelope of magmatism related to the BIC is limited to a series of satellite intrusions in southern Africa and has not been traced further afield. This appears inconsistent with the inferred large size of the BIC event. Here, we present new radiometric ages for alkaline magmatism in the Archean Yilgarn Craton (Western Australia), which overlap the emplacement age of the BIC and indicate a much more extensive geographic footprint of the BIC magmatic event. To assess plume involvement at this distance, we present numerical simulations of mantle plume impingement at the base of the lithosphere, and constrain a relationship between the radial extent of volcanism versus time, excess temperature and plume size. These simulations suggest that the thermal influence of large plume events could extend for thousands of km within a few million years, and produce widespread alkaline magmatism, crustal extension potentially leading to continental break-up, and large ore deposits in distal sectors. Our results imply that superplumes may produce very extensive and diverse magmatic and metallogenic provinces, which may now be preserved in widely-dispersed continental blocks.
Abstract: 2.9 Ga is an uncommon magmatic age in Archean evolution worldwide, especially in West Gondwana. We identified so far unknown 2.97-2.92 Ga high?K calc?alkaline magmatism in the Borborema Province, northeast Brazil. It appears to indicate that the transition to high?K magmas occurred before c. 2.7 Ga in Earth's history. The 2.9 Ga protoliths were reworked and progressively changed composition to 2.65 Ga and 2.25 Ga higher?K granites in early magmatic arcs. Therefore, despite several reworking events from the Archean to Proterozoic times, these rare relicts of K?rich magmatism indicate that reworking of felsic components was significant for the growth and differentiation of continental crust from c. 2.9 Ga onwards in West Gondwana.
Geology of Ore Deposits, Vol. 62,8, pp. 704-718. pdf
Russia, Canada
alkaline rocks
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.
Abstract: On the basis of petrographic and mineralogical studies, we have established the presence of clastic rocks with a strong predominance of K-feldspar among the rock-forming fragments within the Late Precambrian sedimentary sequence in the southwestern part of the Siberian Platform. Two types of mineralogical occurrence of K-feldspars are determined: (1) huge zonal crystal clasts with increased Ba concentrations in the central parts of the grains and (2) the main mineral phase in the form of a decrystallized glassy mass. In both cases, low concentrations of Na (lower than 0.1 wt %) are detected. K-feldspars of the second type contain intergrowths of idiomorphic rhombic dolomite with a high ankerite component. Dolomite grains contain inclusions of K-feldspar. The prevailing accessory minerals are F-apatite (with high concentrations of REEs), zircon (with high concentrations of Th), magnetite, rutile, monacite, and sinchizite. Encasement minerals with an idiomorphic shape are identified, with K-feldspar being located in the center, while the middle shell is formed by apatite with a high REE content, and the outer shell is formed by apatite without rare earth elements. These rocks are products of high-potassium volcanic activity. The age of this event has been established on the basis of U-Pb zircon dating to about 640 Ma. The Lu-Hf zircon systematics for these rocks indicates the connection of volcanism with igneous events of mantle genesis within its range. The products of explosive eruption, which are widespread within the Biryusa uplift of the Siberian Platform, were erroneously considered earlier as Riphean sedimentary rocks of the Karagas Series.
Contributions to Mineralogy and Petrology, 176, 21p. Pdf
India
alkaline rocks
Abstract: Strongly SiO2-undersaturated alkalic rocks (Mg#?>?50, SiO2???45 wt%, Na2O?+?K2O???3 wt%) occur in three early-stage (Sarnu-Dandali, Mundwara, Bhuj) and one late-stage (Murud-Janjira) rift-associated volcanic complexes in the Cretaceous-Paleogene Deccan Traps flood basalt province of India. Thermobarometry based on clinopyroxene-liquid equilibrium suggests that they mostly crystallized beneath the Moho at?~?15 kbar/1270 °C to?~?11-12 kbar/1115-1156 °C pressures and temperatures. Primary magma compositions in equilibrium with lherzolite were estimated through reverse fractionation calculations by incrementally adding equilibrium phases to the rocks in olivine:clinopyroxene:spinel:phlogopite?=?12:68:20:15 proportions at low temperatures followed by olivine:clinopyroxene:spinel?=?12:68:20 proportions at higher temperatures. A comparison of the primary magmas with experimentally generated melts shows that their compositions are consistent with an origin from garnet lherzolite sources with?
Abstract: The Cretaceous High Arctic Large Igneous Province (HALIP) in Canada, although dominated by tholeiites (135-90?Ma), contains two main groups of alkaline igneous rocks. The older alkaline rocks (?96?Ma) scatter around major fault and basement structures. They are represented by the newly-defined Fulmar Suite alkaline basalt dykes and sills, and include Hassel Formation volcanics. The younger alkaline group is represented by the Wootton Intrusive Complex (92.2-92.7?Ma), and the Audhild Bay Suite (83-73?Ma); both emplaced near the northern coast of Ellesmere Island. Fulmar Suite rocks resemble EM-type ocean island basalts (OIB) and most show limited crustal contamination. The Fulmar Suite shows increases of P2O5 at near-constant Ba-K-Zr-Ti that are nearly orthogonal to predicted fractionation- or melting-related variations; which we interpret as the result of melting composite mantle sources containing a regionally widespread apatite-bearing enriched component (P1). Low-P2O5 Fulmar Suite variants overlap compositionally with enriched HALIP tholeiites, and fall on common garnet lherzolite trace element melting trajectories, suggesting variable degrees of melting of a geochemically similar source. High-P2O5 Hassel Formation basalts are unusual among Fulmar rocks, because they are strongly contaminated with depleted lower crust; and because they involve a high-P2O5-Ba-Eu mantle component (P2), similar to that seen in alkali basalt dykes from Greenland. The P2 component may have contained Ba-Eu-rich hawthorneite and/or carbonate minerals as well as apatite, and may typify parts of the Greenlandic sub-continental lithospheric mantle (SCLM). Mafic alkaline Audhild Bay Suite (ABS) rocks are volcanic and hypabyssal basanites, alkaline basalts and trachy-andesites, and resemble HIMU ocean island basalts in having high Nb, low Zr/Nb and low 87Sr/86Sri. These mafic alkaline rocks are associated with felsic alkaline lavas and syenitic intrusions, but crustally-derived rhyodacites and rhyolites also exist. The Wootton Intrusive Complex (WIC) contains geochemically similar plutonic rocks (alkali gabbros, diorites and anatectic granites), and may represent a more deeply eroded, slightly older equivalent of the ABS. Low-P2O5 ABS and WIC alkaline mafic rocks have flat heavy rare-earth (HREE) profiles suggesting shallow mantle melting; whereas High-P2O5 variants have steep HREE profiles indicating deeper separation from garnet-bearing residues. Some High-P2O5 mafic ABS rocks seem to contain the P1 and P2 components identified in Fulmar-Hassel rocks, whereas other samples trend towards possible High-P2O5+Zr (PZr) and High-P2O5+K2O (PK) components. We argue that the strongly alkaline northern Ellesmere Island magmas sampled mineralogically heterogeneous veins or metasomes in Greenlandic-type SCLM, which contained trace phases like apatite, carbonates, hawthorneite, zircon, mica or richterite. The geographically more widespread apatite-bearing component (P1), could have formed part of a heterogeneous plume or upwelling mantle current that also generated HALIP tholeiites when melted more extensively, but may also have resided in the SCLM as relics of older events. Rare HALIP alkaline rocks with high K-Rb-U-Th fall on mixing paths implying strong local contamination from either Sverdrup Basin sedimentary rocks or granitic upper crust. However, the scarcity of potassic alkaline HALIP facies, together with the other trace element and isotopic signatures, provide little support for an ubiquitous fossil sedimentary subduction zone component in the HALIP mantle source.
Abstract: The Cretaceous High Arctic Large Igneous Province (HALIP) in Canada, although dominated by tholeiites (135-90?Ma), contains two main groups of alkaline igneous rocks. The older alkaline rocks (?96?Ma) scatter around major fault and basement structures. They are represented by the newly-defined Fulmar Suite alkaline basalt dykes and sills, and include Hassel Formation volcanics. The younger alkaline group is represented by the Wootton Intrusive Complex (92.2-92.7?Ma), and the Audhild Bay Suite (83-73?Ma); both emplaced near the northern coast of Ellesmere Island. Fulmar Suite rocks resemble EM-type ocean island basalts (OIB) and most show limited crustal contamination. The Fulmar Suite shows increases of P2O5 at near-constant Ba-K-Zr-Ti that are nearly orthogonal to predicted fractionation- or melting-related variations; which we interpret as the result of melting composite mantle sources containing a regionally widespread apatite-bearing enriched component (P1). Low-P2O5 Fulmar Suite variants overlap compositionally with enriched HALIP tholeiites, and fall on common garnet lherzolite trace element melting trajectories, suggesting variable degrees of melting of a geochemically similar source. High-P2O5 Hassel Formation basalts are unusual among Fulmar rocks, because they are strongly contaminated with depleted lower crust; and because they involve a high-P2O5-Ba-Eu mantle component (P2), similar to that seen in alkali basalt dykes from Greenland. The P2 component may have contained Ba-Eu-rich hawthorneite and/or carbonate minerals as well as apatite, and may typify parts of the Greenlandic sub-continental lithospheric mantle (SCLM). Mafic alkaline Audhild Bay Suite (ABS) rocks are volcanic and hypabyssal basanites, alkaline basalts and trachy-andesites, and resemble HIMU ocean island basalts in having high Nb, low Zr/Nb and low 87Sr/86Sri. These mafic alkaline rocks are associated with felsic alkaline lavas and syenitic intrusions, but crustally-derived rhyodacites and rhyolites also exist. The Wootton Intrusive Complex (WIC) contains geochemically similar plutonic rocks (alkali gabbros, diorites and anatectic granites), and may represent a more deeply eroded, slightly older equivalent of the ABS. Low-P2O5 ABS and WIC alkaline mafic rocks have flat heavy rare-earth (HREE) profiles suggesting shallow mantle melting; whereas High-P2O5 variants have steep HREE profiles indicating deeper separation from garnet-bearing residues. Some High-P2O5 mafic ABS rocks seem to contain the P1 and P2 components identified in Fulmar-Hassel rocks, whereas other samples trend towards possible High-P2O5+Zr (PZr) and High-P2O5+K2O (PK) components. We argue that the strongly alkaline northern Ellesmere Island magmas sampled mineralogically heterogeneous veins or metasomes in Greenlandic-type SCLM, which contained trace phases like apatite, carbonates, hawthorneite, zircon, mica or richterite. The geographically more widespread apatite-bearing component (P1), could have formed part of a heterogeneous plume or upwelling mantle current that also generated HALIP tholeiites when melted more extensively, but may also have resided in the SCLM as relics of older events. Rare HALIP alkaline rocks with high K-Rb-U-Th fall on mixing paths implying strong local contamination from either Sverdrup Basin sedimentary rocks or granitic upper crust. However, the scarcity of potassic alkaline HALIP facies, together with the other trace element and isotopic signatures, provide little support for an ubiquitous fossil sedimentary subduction zone component in the HALIP mantle source.
Abstract: Syn-exhumation mafic magmatism during continental collision provides insights into the crust-mantle reaction during deep subduction and the nature of orogenic lithospheric mantle in collisional orogens. In this study, we present a comprehensive data set of zircon U-Pb ages and whole-rock major-trace elements as well as Sr-Nd-Pb isotopes of alkaline mafic rocks from the southern Liaodong Peninsula, eastern China. Zircon U-Pb analyses yield Late Triassic age of 213 ± 3 to 217 ± 3 Ma, younger than the Middle Triassic ultrahigh-pressure metamorphic rocks of the Dabie-Sulu orogen. Thus, the alkaline mafic rocks are products of syn-exhumation magmatism during continental collision of the South and North China blocks. The rocks show shoshonitic affinities with high K2O (3.78-5.23 wt%) and K2O/Na2O (0.71-1.22). They are characterized by arc-like trace-element patterns with enriched LILE, Pb, and LREE, and depleted HFSE. They exhibit enriched Sr-Nd isotopic compositions with high initial 87Sr/86Sr isotopic ratios of 0.7058-0.7061 and negative ?Nd(t) values of ?13.0 to ?15.1. These results suggest involvement of recycled continental crust in their mantle source. The mantle source likely formed by the metasomatic reaction of subducted continental crust-derived melts with the overlying subcontinental lithospheric mantle during the Triassic continental collision. Decompressional melting of this metasomatized mantle formed syn-exhumation mafic magmas during the transition from convergent to extensional tectonics in the Late Triassic. Accordingly, mafic rocks from the southern Liaodong Peninsula provide a geochemical record of the subduction and recycling of continental crust into the mantle and melt-mantle reaction induced metasomatism within the orogen.
Abstract: General information is presented on ten agpaitic occurrences located in southern Brazil and at the border between Brazil and Paraguay. All the Brazilian agpaitic rocks are Late Cretaceous in age, whereas the Paraguayan ones are older than Early Triassic. The most significant occurrence is Poços de Caldas, the largest alkaline massif in South America. In general, these agpaitic rocks contain mineral assemblages that indicate presence of typical halogen-bearing Na-Ca-HFSE phases, eudialyte-, rinkite- and wöhlerite-group minerals being the most frequent ones. However, these associations are indeed more complex in terms of composition, with accessory phases in some cases consisting of various minerals, including U-Th oxides/silicates, Nb oxides, REE-Sr-Ba bearing carbonates-fluorocarbonates-phosphates-silicates and Zr-Na rich silicates. They usually form late magmatic stage to hydrothermal/deuteric assemblages linked with coarse and fine-grained, mainly silica-undersaturated evolved rocks. Data also indicate significant differences in type, amount and composition of agpaitic minerals in all investigated occurrences.
Abstract: The Cretaceous High Arctic Large Igneous Province (HALIP) in Canada, although dominated by tholeiites (135-90?Ma), contains two main groups of alkaline igneous rocks. The older alkaline rocks (?96?Ma) scatter around major fault and basement structures. They are represented by the newly defined Fulmar Suite alkaline basalt dykes and sills, and include Hassel Formation volcanic rocks. The younger alkaline group is represented by the Wootton Intrusive Complex (92•2-92•7?Ma), and the Audhild Bay Suite (83-73?Ma), both emplaced near the northern coast of Ellesmere Island. Fulmar Suite rocks resemble EM-type ocean island basalts (OIB) and most show limited crustal contamination. The Fulmar Suite shows increases of P2O5 at near-constant Ba-K-Zr-Ti that are nearly orthogonal to predicted fractionation- or melting-related variations, which we interpret as the result of melting composite mantle sources containing a regionally widespread apatite-bearing enriched component (P1). Low-P2O5 Fulmar Suite variants overlap compositionally with enriched HALIP tholeiites, and fall on common garnet lherzolite trace element melting trajectories, suggesting variable degrees of melting of a geochemically similar source. High-P2O5 Hassel Formation basalts are unusual among Fulmar rocks, because they are strongly contaminated with depleted lower crust; and because they involve a high-P2O5-Ba-Eu mantle component (P2), similar to that seen in alkali basalt dykes from Greenland. The P2 component may have contained Ba-Eu-rich hawthorneite and/or carbonate minerals as well as apatite, and may typify parts of the Greenlandic sub-continental lithospheric mantle (SCLM). Mafic alkaline Audhild Bay Suite (ABS) rocks are volcanic and hypabyssal basanites, alkaline basalts and trachy-andesites, and resemble HIMU ocean island basalts in having high Nb, low Zr/Nb and low 87Sr/86Sri. These mafic alkaline rocks are associated with felsic alkaline lavas and syenitic intrusions, but crustally derived rhyodacites and rhyolites also exist. The Wootton Intrusive Complex (WIC) contains geochemically similar plutonic rocks (alkali gabbros, diorites and anatectic granites), and may represent a more deeply eroded, slightly older equivalent of the ABS. Low-P2O5 ABS and WIC alkaline mafic rocks have flat heavy rare earth element (HREE) profiles suggesting shallow mantle melting; whereas High-P2O5 variants have steep HREE profiles indicating deeper separation from garnet-bearing residues. Some High-P2O5 mafic ABS rocks seem to contain the P1 and P2 components identified in Fulmar-Hassel rocks, whereas other samples trend towards possible High-P2O5 + Zr (PZr) and High-P2O5 + K2O (PK) components. We argue that the strongly alkaline northern Ellesmere Island magmas sampled mineralogically heterogeneous veins or metasomes in Greenlandic-type SCLM, which contained trace phases such as apatite, carbonates, hawthorneite, zircon, mica or richterite. The geographically more widespread apatite-bearing component (P1) could have formed part of a heterogeneous plume or upwelling mantle current that also generated HALIP tholeiites when melted more extensively, but may also have resided in the SCLM as relics of older events. Rare HALIP alkaline rocks with high K-Rb-U-Th fall on mixing paths implying strong local contamination from either Sverdrup Basin sedimentary rocks or granitic upper crust. However, the scarcity of potassic alkaline HALIP facies, together with the other trace element and isotopic signatures, provides little support for a ubiquitous fossil sedimentary subduction-zone component in the HALIP mantle source.
Abstract: Alkaline igneous rocks host many global high-field-strength element (HFSE) and rare-earth element (REE) deposits. While HFSEs are commonly assumed to be immobile in hydrothermal systems, transport by late-stage hydrothermal fluids associated with alkaline magmas is reported. However, the magnitude of the flux and the conditions are poorly constrained and yet essential to understanding the formation of REE-HFSE ores. We examined the alteration of country rocks (“fenitization”) accompanying the emplacement of a syenite magma at Illerfissalik in Greenland, through analysis of changes in rock chemistry, mineralogy, and texture. Our novel geochemical maps show a 400-m-wide intrusion aureole, within which we observed typically tenfold increases in the concentrations of many elements, including HFSEs. Textures suggest both pervasive and structurally hosted fluid flow, with initial reaction occurring with the protolith's quartz cement, leading to increased permeability and enhancing chemical interaction with a mixed Ca-K-Na fenitizing fluid. We estimated the HFSE masses transferred from the syenite to the fenite by this fluid and found ~43 Mt of REEs were mobilized (~12% of the syenite-fenite system total rare-earth-oxide [TREO] budget), a mass comparable to the tonnages of some of the world's largest HFSE resources. We argue that fenite can yield crucial information about the tipping points in magma evolution because retention and/or loss of volatile-bonded alkali and HFSEs are key factors in the development of magmatic zirconosilicate-hosted HFSE ores (e.g., Kringlerne, at Ilímaussaq), or the formation of the syenite-hosted Nb-Ta-REE (Motzfeldt-type) roof-zone deposits.
