Based on the field relations, associated rock types and age, the carbonatite-alkaline rock complexes of India, that are spatially related to deep main faults, rifts and shear zones, have been classified in to two major groups, namely: 1. Middle — late Cretaceous, subvolcanic -volcanic complexes (Amba Dongar, Siriwasan, Swangkre, Mer-Mundwara, Sarnu-Dandali-Kamthai) and 2. Paleo-Neoproterozoic plutonic complexes (Newania, Sevathur, Samalpatti, Hogenakal, Kollegal, Pakkanadu, Udaiyapatti, Munnar, and Khambamettu). The middle Cretaceous Sung Valley and Samchampi complexes also belong to this plutonic group. Three minor associations, belonging to these two age groups include, the Neoproterzoic, late stage veins of carbonatites in peralkaline syenite complexes (e.g., Kunavaram, Elchuru), the diamond-bearing carbonatite and kimberlite at Khaderpet and the lamprophyre-lamproite association (e.g., Pachcham Is. Upper Cretaceous, Deccan Volcanic Province, and the Proterozoic Chitrangi Group). Petrological associations include carbonatite-nephelinite-phonolite (e.g. Amba Dongar, Sarnu-Dandali-Kamthai), dunite-peridotite-pyroxenite-ijolitemelilitite (e.g. Sung Valley), miaskitic syenite-pyroxenite ± dunite (e.g. Sevathur, Samalpatti, Pakkanadu), carbonatite alone with fenites (e.g. Newania), besides those minor associations mentioned above. Sovites (calico-carbonatites) occur as the most dominant type in some ten (10) complexes. Beforsite (magnesio-carbonatite) is the dominant type at Newania and ankeritic-sideritic types are mainly found at Amba Dongar, Siriwasan and Newania. The rare benstonite-bearing carbonatites are found at Jokkipatti and Udaiyapatti in Tamil Nadu. Mineralogically and chemically the carbonatites show considerable diversity. Fenitised zones and types of fenites (Na, K and mixed) vary widely since the carbonatites are emplaced in a variety of hostrocks ranging from granitic, mafic, ultramafic, charnockitic types besides basalts and sandstones. Stable (δ13C and δ18O) and radiogenic (Sr, Nd and Pb) isotopes clearly indicate their mantle origin and also the diverse types of sources (both depleted HIMU and enriched EM 1 and 2). Petrogenetic considerations reveal three types of carbonatites, namely direct partial melts from metasomatised mantle (e.g. Newania), liquid immiscibility from carbonatite-nephelinite association (e.g. Amba Dongar) and through fractionation of ultra-alkaline ultramafic and mafic association (e.g. Sung Valley). Carbonatites of India that host significant resources include Amba Dongar (Fluorite, REE, Nb, P, Ba, Sr), Kamthai (REE), Sevathur (Nb, P, vermiculite), Beldih (P, Fe), Sung Valley (P, Nb, REE, Fe) and Samchampi (P, Nb, Fe, REE).

Carbonatites of India

Approximately >50% of global rare earth element (REE) resources are hosted by carbonatite related deposits, of which monazite is one of the most important REE minerals. Monazite dominates more than 30 carbonatite-related REE deposits around the world, including currently exploited mineralization at Bayan Obo and Mount Weld. These deposits are widely distributed across all continents, except Antarctica. Though rare, monazite occurs as the primary mineral in carbonatite, and mostly presents as a secondary mineral that has a strong association with apatite. It can partially or completely replace thin or thick overgrowth apatite, depending on the availability of REE. Other mineral phases that usually crystallize together with monazite include barite, fluorite, xenotime, sulfide, and quartz in a carbonate matrix (e.g., dolomite, calcite). This review of monazite geochemistry within carbonatite-related REE deposits aims to provide information regarding the use of monazite as a geochemical indicator to track the formation history of the REE deposits and also supply additional information for the beneficiation of monazite. The chemical compositions of monazite are highly variable, and Ce-monazite is the dominant solid solution in carbonatite related deposits. Most monazite displays steep fractionation from La to Lu, absent of either Eu or Ce anomalies in the chondrite normalized REE plot. The other significant components are huttonite and cheratite. Some rare sulfur-bearing monazite is also identified with an SO3 content up to 4 wt %. A 147Sm/144Nd ratio with an average ~0.071 for monazite within carbonatite-related ores is similar to that of their host rocks (~0.065), and is the lowest among all types of REE deposits. Sm/Nd variation of monazite from a single complex reflects the differentiation stage of magma, which decreases from early to late. Based on the differences of Nd and Sr abundances, Nd isotopic composition for monazite can be used to track the magma source, whereas Sr isotopic composition records the signatures of the fluid source. Th-(U)-Pb age determination of the secondary monazite records variable thermal or metasomatic disturbances, and careful geochronological interpretation should be brought forward combined with other lines of evidence. ThO2 is the most difficult contamination in the beneficiation of monazite, luckily, the ThO2 content of monazite within carbonatite is generally low (<2 wt %).

Geochemistry of Monazite within Carbonatite Related REE Deposits

Abstract Carbonatites are carbonate-rich rocks of igneous origin. They form the magmas of their own that are generated in the deep mantle by low degrees of partial melting of carbonated peridotite or eclogite source rocks. They are known to occur since the Archaean times till recent, the activity showing gradual increase from older to younger times. They are commonly associated with alkaline rocks and be genetically related with them. They often induce metasomatic alteration in the country rocks forming an aureole of fenitization around them. They are host for economically important mineral deposits including rare metals and REE. They are commonly associated with the continental rifts, but are also common in the orogenic belts; but not known to occur in the intra-plate regions. The carbonatites are known to occur all over the globe, majority of the occurrences located in Africa, Fenno-Scandinavia, Karelian-Kola, Mongolia, China, Australia, South America and India. In the Indian Subcontinent carbonatites occur in India, Pakistan, Afghanistan and Sri Lanka; but so far not known to occur in Nepal, Bhutan, Bangladesh and Myanmar. This paper takes an overview of the carbonatite occurrences in the Indian Subcontinent in the light of recent data. The localities being discussed in detail cover a considerable time range (>2400 Ma to <0.6 Ma) from India (Hogenakal, Newania, Sevathur, Sung Valley, Sarnu-Dandali and Mundwara, and Amba Dongar), Pakistan (Permian Koga and Tertiary Pehsawar Plain Alkaline Complex which includes Loe Shilman, Sillai Patti, Jambil and Jawar), Afghanistan (Khanneshin) and Sri Lanka (Eppawala). This review provide the comprehensive information about geochemical characteristics and evolution of carbonatites in Indian Subcontinent with respect to space and time.

An Overview of the Carbonatites from the Indian Subcontinent

Characterization of organic matter and its implications for pyrite hosted refractory gold mineralization along the South Purulia Shear Zone, eastern India

Major highlights of researches carried out on kimberlites, lamproites, lamprophyres, carbonatites, other alkaline rocks and mafic dykes from the Indian shield during 2012-2016 are presented. New findings involving field mapping, petrology , geochemistry (including high quality mineral based in situ isotopic studies) and geophysics have provided remarkable insights on the mode of their occurrence, timing of emplacement, mineralogy and bulk-rock composition, redox conditions, relative contribution of the lithosphere and asthenosphere, as well as their economic potential. Several large-scale geodynamic aspects such as plume-lithosp here interactions, ancient subduction events, layered structure of the sub-continental lithospheric mantle, spatial extent of the Precambrian large igneous provinces and supercontinent configurations could be unraveled from these studies on deep-mantle derived small-volume magmatic rocks.

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Kimberlites, Lamproites, Lamprophyres, Carbonatites, other Alkaline Rocks, and Mafic Dykes from the Indian Shield: Glimpses of Research (2012-2016)

The variant rock types of an Alkaline-Carbonatite Complex (ACC) comprising alkali pyroxenite, nepheline syenite, phoscorite, carbonatite, syenitic fenite and glimmerite along with REE and Nb-mineralization are found at different centres along WNW-ESE trending South Purulia Shear Zone (SPSZ) in parts of Singhbhum Crustal Province. The ACC occurs as intrusions within the Mesoproterozoic Singhbhum Group of rocks. Alkali pyroxenite comprises of aegirine augite, magnesiotaramite, magnesiokatophorite as major constituents. Pyrochlore and eucolite are ubiquitous in nepheline syenite. Phoscorite contains fluorapatite, dahllite, collophane, magnetite, hematite, goethite, phlogopite, calcite, sphene, monazite, pyrochlore, chlorite and quartz. Coarse fluorapatite shows overgrowth of secondary apatite (dahllite). Secondary apatite is derived from primary fluorapatite by solution and reprecipitation. The primary fluorapatite released REE to crystallize monazite grains girdling around primary apatite. Carbonatite is composed dominantly of Srcalcite along with dolomite, tetraferriphlogopite, phlogopitic biotite, aegirine augite, richterite, fluorapatite, altered magnetite, sphene and monazite. The minerals comprising of the carbonatite indicate middle stage of carbonatite development. Fenite is mineralogically syenite. Glimmerite contains 50–60% tetraferriphlogopite. An alkali trend in the evolution of amphiboles (magnesiotaramite-magnesiokatophorite-richterite) and chinopyroxenes (aegirine augite, aegirine) during the crystallization of the suite of rocks is noted. Monazite is the source of REE in phoscorite and carbonatite. Fluorapatite has low contents of REE, PbO, ThO2 and UO2. Pyrochlore reflects Nb-mineralization in nepheline syenite and it is enriched in Na2O, CaO, TiO2, PbO and UO2. Pyrochlore containing UO2 (6.605%) and PbO (0.914%) in nepheline syenite has been chemically dated at 948 ± 24 Ma by EPMA.

S. K. Basu

Papers

Petrography and mineral chemistry of Alkaline-Carbonatite Complex in Singhbhum Crustal Province, Purulia region, Eastern India