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Petrogenesis of a nepheline syenite from parts of the Chotanagpur Granite Gneissic Complex: implications for Neoproterozoic crustal extension in the East Indian Shield

Published online by Cambridge University Press:  28 April 2022

Satabdi Das*
Affiliation:
Department of Geological Sciences, Jadavpur University, Kolkata, 700032, India
Deepak K Sinha
Affiliation:
Atomic Minerals Directorate for Exploration and Research, Hyderabad, 500016, India
Sanjoy Sanyal
Affiliation:
Department of Geological Sciences, Jadavpur University, Kolkata, 700032, India
Subrata Karmakar
Affiliation:
Department of Geological Sciences, Jadavpur University, Kolkata, 700032, India
Biswajit Panigrahi
Affiliation:
Atomic Minerals Directorate for Exploration and Research, Jamshedpur, 831002, India
Sirina Roy Choudhury
Affiliation:
Department of Geological Sciences, Jadavpur University, Kolkata, 700032, India
Shyamal Sengupta
Affiliation:
Department of Geological Sciences, Jadavpur University, Kolkata, 700032, India
Pulak Sengupta
Affiliation:
Department of Geological Sciences, Jadavpur University, Kolkata, 700032, India
*
Author for correspondence: Satabdi Das, Email: satabdi.jugeol@gmail.com
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Abstract

The North Purulia Shear Zone that dissects the granulite basement of the Chotanagpur Granite Gneissic Complex of the East Indian Shield exposes a deformed and metamorphosed nepheline syenite. The studied ‘foid-monzosyenite’ shows high abundances of large ion lithophile elements and high field strength elements with low abundances of compatible elements. Trace-element signatures show negative U, Th, Zr, Ti and Pb and positive Sr, Ba and Eu anomalies with respect to the primitive mantle. The chondrite-normalized diagram shows strongly fractionated rare earth element patterns ((La/Lu)N ∼23–87). Geochemical fingerprints suggest that the basanitic protolith was formed by low-degree partial melting of garnet peridotite in the sub-continental lithospheric mantle. The enriched large ion lithophile, high field strength element and light rare earth element concentrations (relative to primitive mantle) can be explained by a mixed mantle source with components from a previously deformed alkaline rock/carbonatite. Geochemical data do not support any significant crustal contamination and suggest variable fractionation of clinopyroxene, ilmenite, titanite and apatite from the parental melt. Petrological data are consistent with the view that the nepheline syenite magma was emplaced in a rift setting with a minimum temperature of 800–900°C, low fO2 conditions (below the fayalite–magnetite–quartz buffer) at a mid-crustal depth between 950 and 900 Ma. The continental rift zone, however, did not lead to the formation of an open ocean basin. Subsequently, the studied rock and its basement was deformed and metamorphosed in a continent–continent collisional setting at ∼900 Ma. Combining information from the other Indian occurrences with this study, it is demonstrated that the deformed alkaline rocks and carbonatite are potentially valuable for tracing the birth and demise of the palaeo-supercontinents.

Information

Type
Original Article
Copyright
© The Author(s), 2022. Published by Cambridge University Press
Figure 0

Fig. 1. General geological map of the East Indian Shield comprising the Chotanagpur Granite Gneissic Complex (CGGC) in the north, North Singhbhum Fold Belt (NSFB) in the middle and Singhbhum Craton in the south (modified after Acharyya, 2003). The red star shows the occurrence of the studied nepheline syenite in the southern portion of the Domain-IA of the CGGC. MSRF – Monghyr-Saharsa Ridge Fault; EITZ – Eastern Indian Tectonic Zone; NPSZ – North Purulia Shear Zone; SPSZ – South Purulia Shear Zone; SSZ – Singhbhum Shear Zone. Deformed nepheline syenites and carbonatites of the CGGC are marked as blue coloured circles and squares, respectively.

Figure 1

Fig. 2. Simplified litho-structural map showing distribution of alkaline rocks and associated rocks in and around Kankarkiari–Kusumdih village (modified after Das et al. 2019). The sample locations are indicated in white.

Figure 2

Fig. 3. (a) S2 gneissic banding of the host felsic orthogneiss (FOG) swerving around the enclaves of khondalite. S1 foliation of the khondalite enclave abuts against the external S2 foliation at a high angle. (b) Greasy-looking charno-enderbite occurring as a patch in FOG, but with a gradational boundary; continuous S2 foliation can be traced across the boundaries of the two units. (c) Gneissic foliation (S3) in nepheline syenite defined by alternate thin dark, impersistent bands composed of biotite, amphibole and pyroxene and light grey coloured feldspars and nepheline. (d) Megacrystic nepheline and alkali feldspar sprinkled inhomogeneously within a fine-grained groundmass of nepheline-feldspar define relict porphyritic appearance of the rock. (e) The S3 gneissic foliation defined by amphibole and/or biotite is swerving around nepheline porphyroclasts. (f) Secondary shear fabric composed of haphazard biotite grains in the rock.

Figure 3

Fig. 4. (a) Intense deformation modified the pristine orthocumulus texture and developed a granoblastic mosaic of fine recrystallized nepheline (Ne), alkali feldspar (Kfs), plagioclase (Pl), clinopyroxene, magnetite, titanite, apatite and calcite grains with polygonal grain margins. (b) S3 foliation defined by oriented grains of biotite (Bt) and amphibole (Am) swerves past spindle-shaped megacrystic nepheline; perthite with an albite rim occurs as an inclusion within the porphyroclast. (c) Lenticular megacrystic perthite records undulose extinction, bending of lamellae, marginal recrystallization and a core–mantle texture. (d) Back-scattered electron image shows oriented grains of amphibole and biotite replacing the magmatic phases (clinopyroxene (Cpx), plagioclase) as a result of metamorphism. (e) Randomly oriented biotite replaces ilmenite (Ilm), magnetite (Mag) and alkali feldspar along the margins. (f) Cancrinite (Ccn) veinlets replace nepheline grains along the fractures and cleavage planes.

Figure 4

Table 1. Representative oxide analyses (wt %) and calculated cations per formula unit of clinopyroxene

Figure 5

Table 2. Representative oxide analyses (wt %) and calculated cations per formula unit of amphibole

Figure 6

Table 3. Representative oxide analyses (wt %) and calculated cations per formula unit of biotite

Figure 7

Table 4. Representative oxide analyses (wt %) and calculated cations per formula unit of nepheline

Figure 8

Table 5. Representative oxide analyses (wt %) and calculated cations per formula unit of feldspars

Figure 9

Table 6. Representative oxide analyses (wt %) and calculated cations per formula unit of apatite

Figure 10

Table 7. Representative oxide analyses (wt %) and calculated cations per formula unit of magnetite, ilmenite, titanite and calcite

Figure 11

Fig. 5. (a) Clinopyroxene compositions plotted on the Q (quadrilateral pyroxene) – jadeite (Jd) – aegirine (Ac) diagram (Morimoto, 1988). (b) Clinopyroxene compositions extend across the boundaries between diopside–hedenbergite and aegirine–augite on the Na/(Na + Ca) versus AlVI/(AlVI + Fe3+) atoms per formula unit diagram. (c) Amphibole compositions plot in the field of hastingsite to ferro-pargasite on the Mg number versus Si (apfu) diagram for calcic amphiboles by Leake et al. (1997). (d) Nepheline compositions plotted on the normative nepheline (Ne) – kalsilite (Kls) – silica (Qtz) triangular diagram (Tilley, 1954).

Figure 12

Table 8. Representative bulk composition of Kusumdih nepheline syenite

Figure 13

Fig. 6. (a) The studied rock falls in the ‘foid-monzosyenite’ and ‘foid-bearing monzonite’ field on the Feldspathoid – Plagioclase feldspar – Alkali feldspar (FAP) diagram (Le Maitre, 2002). (b) The Total Alkali Silica (TAS) diagram suggests that most of the samples are of ‘nepheline syenite’; with some plotting in between the fields of ijolite and gabbro (Le Bas et al. 1992). (c) The samples plot in the ‘shoshonite’ field on the K2O versus silica diagram (Peccerillo & Taylor, 1976). (d) The molar A/NK versus A/CNK diagram reveals that the rock samples are ‘metaluminous’ to ‘peralkaline’ in nature (Shand, 1943). (e) Samples appear to be slightly miaskitic when plotted on the Agpaitic index (molar Na + K/Al) versus SiO2 plot. Fields for bulk-rock data from other DARs from India (Upadhyay & Raith, 2006; Upadhyay et al. 2006a,b,c) have been included in diagrams (a–d).

Figure 14

Fig. 7. (a) Primitive-mantle normalized trace-element spidergram (after McDonough & Sun, 1995) and (b) chondrite-normalized rare earth element diagram (after McDonough & Sun, 1995) for the studied rock.

Figure 15

Fig. 8. Selected bivariate diagrams and plots showing the trends in major- and trace-element concentrations. Symbols used for the samples are the same as in Figure 6.

Figure 16

Fig. 9. Variation diagrams of major oxides with concentration of Mg no. (Differentiation Index) showing positive variation trends for SiO2, TiO2, FeO, CaO and P2O5, a negative trend for Na2O and scatter for K2O and Al2O3. Symbols used for the samples are the same as in Figure 6.

Figure 17

Fig. 10. Trace-element variation diagrams with concentration of Mg no. (Differentiation Index). Symbols used for the samples are the same as in Figure 6.

Figure 18

Fig. 11. Primitive-mantle normalized trace-element spidergram for the studied rock compared with (a) the nepheline syenite occurrences in India, and (b) the nepheline syenite occurrences from across the world. Chondrite-normalized rare earth element diagram for the studied rock compared with (c) the nepheline syenite occurrences in India, and (d) the nepheline syenite occurrences from across the world. Average values are plotted for other occurrences, whereas a zone has been marked for the studied rock (Eby et al. 1998; Upadhyay & Raith, 2006; Upadhyay et al. 2006a,b,c; Casquet et al. 2008; Nude et al. 2009; Obeid & Lalonde, 2013; Viana & Battilani, 2014; Cheng et al. 2018).

Figure 19

Fig. 12. (a) Al and Ti content of the clinopyroxene, which suggest the crystallizing pressure of the clinopyroxene from the studied rock was below 10 kbar (Thompson, 1974). The squares represent the experimental pressures in terms of Ti and Al content of clinopyroxene. (b) Apatite saturation temperature gives an estimate of the near liquidus temperature for the alkaline magma of 900°C (Green & Watson, 1982). (c) log fO2 versus temperature diagram in the activity constrained CFTSO system indicates low oxygen fugacity conditions for the crystallization of the alkaline magma, below the FMQ buffer, within the stability field of hedenbergite, ilmenite, titanite and magnetite (Wones, 1989; Lindsley, 1991).

Figure 20

Fig. 13. Schematic diagram of the evolutionary model illustrating the petrogenesis of the studied deformed nepheline syenite showing the (a) formation of the high-grade rocks with the prominent S2 fabric in a continent–continent collision at 1000–950 Ma. (b1) Generation of a basanitic magma by low-degree partial melting of sub-continental lithospheric mantle (SCLM, compositionally garnet peridotite) in a continental rift setting. (b2) Further crystal fractionation of clinopyroxene, apatite, ilmenite, titanite and zircon produced the nepheline syenite (blue) magma that was emplaced in the crust at 950–900 Ma. (c) Rifting failed and the nepheline syenite along with the basement it includes was deformed and metamorphosed in another continent–continent collision at ∼900 Ma.

Figure 21

Fig. 14. Emplacement and metamorphic ages of Proterozoic alkaline rocks and carbonatites of India showing relationship of their emplacement and metamorphism with major supercontinent cycles. Detailed information on these localities is given in Paul et al. (2020).