Potassic glass and calcite carbonatite in lapilli from extrusive carbonatites at Rangwa Caldera Complex, Kenya

2003 ◽  
Vol 67 (5) ◽  
pp. 931-955 ◽  
Author(s):  
G. Rosatelli ◽  
F. Wall ◽  
M. J. Le Bas

AbstractThe ∽16 Ma Rangwa Caldera Complex, part of the large Kisingiri nephelinite-carbonatite volcano, Homa Bay District, western Kenya (0º34’S; 34º09’E) contains carbonatitic lapilli and ash tuffs, agglomerate and tuffisite, and a number of intrusive calcite carbonatites. A detailed petrographic and electron microprobe study has been performed on 20 fresh samples from the collection at The Natural History Museum, London.Most of the juvenile lapilli and ash particles are either predominantly composed of devitrified silicate glass (now biotite/phlogopite but probably also originally potassic silicate) or calcite carbonatite, which suggests that two molten liquids were erupted simultaneously. Some 10 mm-diameter lapilli contain quench-textured calcite crystals set in devitrified glass. They are interpreted as having crystallized from a molten silicate-carbonate melt at, or very near, the surface.The extrusive carbonate is mostly composed of calcite, consistent with intrusive calcite compositions at Rangwa. Other key minerals are magnetite, two types of mica (magnesian-biotite phenocrysts and phlogopite xenocrysts) and fluorapatite.The pyroclastic rocks contain many calcite carbonatite clasts, and fragments of calcite, aegirine and diopside, fluorapatite, magnetite, plus some phlogopite, titanite, K-feldspar, fenite and glimmerite; ijolite lithics are rare. Thus, there is no evidence for a cognate nephelinitic (ijolitic) or melilitic magma nor evidence for a direct relationship with the nephelinites of the Kisingiri volcano.Two hypotheses are discussed. A rising silicate and K-rich carbonatite liquid may have evolved towards a carbonate-rich K-silicate liquid after crystallization of calcite, phlogopite, apatite and magnetite. Preservation of the the potassic component may be rare, with a more usual scenario being that potassic component separates as fenitizing fluids. The alternative is that the silicate component is remobilized fenite, formed from country rock that was mobilized by supercritical K-rich, fenitizing fluids associated with the carbonatite. Both scenarios require generation of a K-rich carbonatite magma, probably from a carbonated phlogopite-rich metasomatized mantle.

Minerals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 654
Author(s):  
Eugene V. Sklyarov ◽  
Andrey V. Lavrenchuk ◽  
Anna G. Doroshkevich ◽  
Anastasia E. Starikova ◽  
Sergei V. Kanakin

Pyroxenite and nepheline-pyroxene rocks coexist with dolomite-bearing calcite marbles in Tazheran Massif in the area of Lake Baikal, Siberia, Russia. Pyroxenites occur in a continuous elongate zone between marbles and beerbachites (metamorphosed gabbro dolerites) and in 5 cm to 20 m fragments among the marbles. Pyroxene in pyroxenite is rich in calcium and alumina (5–12 wt% Al2O3) and has a fassaite composition. The Tazheran pyroxenite may originate from a mafic subvolcanic source indicated by the presence of remnant dolerite found in one pyroxenite body. This origin can be explained in terms of interaction between mafic and crust-derived carbonatitic melts, judging by the mineralogy of pyroxenite bodies and their geological relations with marbles. According to this model, the intrusion of mantle mafic melts into thick lower crust saturated with fluids caused partial melting of silicate-carbonate material and produced carbonate and carbonate-silicate melts. The fassaite-bearing pyroxenite crystallized from a silicate-carbonate melt mixture which was produced by roughly synchronous injections of mafic, pyroxenitic, and carbonate melt batches. The ascending hydrous carbonate melts entrained fragments of pyroxenite that crystallized previously at a temperature exceeding the crystallization point of carbonates. Subsequently, while the whole magmatic system was cooling down, pyroxenite became metasomatized by circulating fluids, which led to the formation of assemblages with garnet, melilite, and scapolite.


1970 ◽  
Vol 91 ◽  
pp. 1-26
Author(s):  
B.J Walton ◽  
A.R Arnold

A swarm of thin NW-SE lamprophyric carbonatite dykes of Mesozoic age occurs south of Frederikshåb associated with a contemporaneous, parallel swarm of thick dolerites. Apart from local country rock material, inclusions in the lamprophyric carbonatites are mainly of the following types: 1) Single crystals of olivine which were probably mainly derived from the upper mantle. 2) Relatively unmodified garnet- and pyroxene-granulite nodules brought up from a lower crustal level. 3) Nodules, and single crystals, consisting mainly of hornblende and salite which are considered to have formed by metasomatic reaction between the carbonatite magma and mainly acid to intermediate lower crustal rocks, possibly at relatively low levels in the dykes. Hornblende shows various stages of growth from initially small, iron-rich crystals to larger, iron-poor crystals which have commonly replaced pyroxenes. The pyroxenes show a similar but less pronounced development. 4) Alkaline nodules which are again thought to have developed by metasomatic reaction between the magma and country rock inclusions, but possibly at higher levels in the dykes. 5) Phlogopite megacrysts which may be partly xenocrystal but which are thought to have mainly crystallised from the contaminated magma. Complete chemical analyses of lamprophyric carbonatites and partial analyses of individual minerals are presented.


2000 ◽  
Vol 64 (4) ◽  
pp. 651-661 ◽  
Author(s):  
K. M. Law ◽  
J. D. Blundy ◽  
B. J. Wood ◽  
K. V. Ragnarsdottir

AbstractWe have performed an experimental study of the influence of varying size and charge on cation partitioning between wollastonite and silicate-carbonate melt in the system CaCO3-SiO2. The experimental conditions (3 GPa, 1420°C) lie close to the wollastonite II tc/I tc phase boundary. Results for 1+, 2+, 3+ and 4+ partitioning show parabolic dependence of partition coefficients on ionic radius, which can be fitted to the elastic strain model of Blundy and Wood (1994), wherein partitioning is described using three parameters: site radius (r0), site elasticity (apparent Young's Modulus) and the ‘strain-free’ partition coefficient (D0) for an element with radius r0. The apparent Young's Modulus of the Ca site in wollastonite, obtained from modelling the 2+ partitioning data, is 99±3 GPa, similar to the bulk-crystal value for the polymorph wollastonite I tc. r0 decreases with increasing charge on the substituent cation, while D0 also shows an approximately parabolic dependence on charge, with a maximum for 2+ cations. Partition coefficients for divalent cations Zn, Co, Fe, Cd, Mn and Pb are lower than would be predicted from their ionic radii alone, indicating a preference for the melt. This may be a consequence either of cation-carbonate complexation in the melt, or of the more distorted nature of cation co-ordination environments in melts.


2012 ◽  
Vol 76 (2) ◽  
pp. 411-439 ◽  
Author(s):  
I. P. Solovova ◽  
A. V. Girnis

AbstractThis paper reports an investigation of the crystallization products of K-rich silicate and carbonate melts trapped as melt inclusions in clinopyroxene phenocrysts from the Dunkeldyk alkaline igneous complex in the Tajik Republic. Heating experiments on the melt inclusions suggest that the carbonate melt was formed by liquid immiscibility at 1180°C and ∼0.5 GPa. The carbonate-rich inclusions are dominated by Sr-bearing calcite, and rich in incompatible elements. Most of the silicate minerals are SiO2-poor and rich in K, Ba and Ti. Leucite, kalsilite and aegirine are the earliest magmatic minerals. High Ba and Ti contents in the melt resulted in the crystallization of Ba-rich K-feldspar, titanite, perovskite and Ti-bearing garnet, and the rare Ba-Ti silicates fresnoite and delindeite. The last minerals to crystallize from volatile-rich melts and fluids were aegirine, götzenite, K-Ba- and Ca-Sr-bearing zeolites, fluorite and strontium-rich baryte. Interaction of the early minerals with residual melts and fluids produced Ba-rich phlogopite and Sr-rich apatite.


2019 ◽  
Vol 64 (9) ◽  
pp. 986-994
Author(s):  
А. V. Spivak ◽  
Yu. А. Litvin ◽  
Е. S. Zakharchenko ◽  
D. А. Simonova ◽  
L. S. Dubrovinsky

The peritectic reaction of ringwoodite (Mg,Fe)2SiO4 and silicate-carbonate melt with formation of magnesiowustite (Fe,Mg)O, stishovite SiO2 and Mg, Na, Ca, K-carbonates is revealed by experimental study at 20 GPa of melting relations of the multicomponent MgO-FeO-SiO2-Na2CO3-CaCO3-K2CO3 system of the Earth’s mantle transition zone. A reaction of CaCO3 and SiO2 with the formation of Ca-perovskite CaSiO3 is also detected. It is shown that the peritectic reaction of ringwoodite and melt with the formation of stishovite physic-chemically controls the fractional ultrabasic-basic evolution of both magmatic and diamond-forming systems of the deep horizons of the transition zone up to its boundary with the Earth’s lower mantle.


Minerals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 724
Author(s):  
Anna A. Nosova ◽  
Ludmila V. Sazonova ◽  
Alexey V. Kargin ◽  
Elena O. Dubinina ◽  
Elena A. Minervina

The study reports petrography, mineralogy and carbonate geochemistry and stable isotopy of various types of ocelli (silicate-carbonate globules) observed in the lamprophyres from the Chadobets Uplift, southwestern Siberian craton. The Chadobets lamprophyres are related to the REE-bearing Chuktukon carbonatites. On the basis of their morphology, mineralogy and relation with the surrounding groundmass, we distinguish three types of ocelli: carbonate-silicate, containing carbonate, scapolite, sodalite, potassium feldspar, albite, apatite and minor quartz ocelli (K-Na-CSO); carbonate–silicate ocelli, containing natrolite and sodalite (Na-CSO); and silicate-carbonate, containing potassium feldspar and phlogopite (K-SCO). The K-Na-CSO present in the most evolved damtjernite with irregular and polygonal patches was distributed within the groundmass; the patches consist of minerals identical to minerals in ocelli. Carbonate in the K-Na-CSO are calcite, Fe-dolomite and ankerite with high Sr concentration and igneous-type REE patterns. The Na-CSO present in Na-rich damtjernite with geochemical signature indicates the loss of the carbonate component. Carbonate phases are calcite and Fe-dolomite, and they depleted in LREE. The K-SCO was present in the K-rich least-evolved damtjernite. Calcite in the K-SCO has the highest Ba and the lowest Sr concentration and U-shaped REE pattern. The textural, mineralogical and geochemical features of the ocelli and their host rock can be interpreted as follows: (i) the K-Na-CSO are droplets of an alkali–carbonate melt that separated from residual alkali and carbonate-rich melt in highly evolved damtjernite; (ii) the Na-CSO are droplets of late magmatic fluid that once exsolved from a melt and then began to dissolve; (iii) the K-SCO are bubbles of K-P-CO2 fluid liberated from an almost-crystallised magma during the magmatic–hydrothermal stage. The geochemical signature of the K-SCO carbonate shows that the late fluid could leach REE from the host lamprophyre and provide for REE mobility.


2019 ◽  
Vol 488 (6) ◽  
pp. 640-644
Author(s):  
N. S. Gorbachev ◽  
A. V. Kostyuk ◽  
Yu. B. Shapovalov ◽  
P. N. Gorbachev ◽  
A. N. Nekrasov ◽  
...  

The phase relations in the phlogopite-carbonate system were studied at P = 3.8 GPa, T = 1200-1300 C. The interaction of phlogopite with carbonate melt resulted in the formation of a polymineral association of relic and newly formed phases of the phlogopite-carbonate-clinopyroxene-spinel-garnet composition coexisting with carbonate melt. By increasing the temperature from 1200 to 1300 C in the carbonate melt increases the solubility of phlogopite and the concentrations of its components - Si, Al, Mg, K. The phase composition of the quenching phases of the carbonate melt varies from substantially carbonate with isolated microcrystals of apatite and phlogopite at 1200 C to phlogopite-carbonate with a variety of texture ratios at 1300 C, reflecting the spontaneous crystallization of the carbonate melt during quenching. In the studied P-T, close to the mantle adiabate, phlogopite remains stable in the presence of silicate-carbonate melt.


Sign in / Sign up

Export Citation Format

Share Document