International Journal of Mineralogy

International Journal of Mineralogy / 2014 / Article

Research Article | Open Access

Volume 2014 |Article ID 978793 | https://doi.org/10.1155/2014/978793

Maitrayee Chakraborty, Sayan Biswas, Nandini Sengupta, Pulak Sengupta, "First Report of Florencite from the Singhbhum Shear Zone of the East Indian Craton", International Journal of Mineralogy, vol. 2014, Article ID 978793, 8 pages, 2014. https://doi.org/10.1155/2014/978793

First Report of Florencite from the Singhbhum Shear Zone of the East Indian Craton

Academic Editor: M. Arima
Received29 Jun 2013
Accepted06 Nov 2013
Published03 Feb 2014

Abstract

Metamorphic florencite is being reported from kyanite-rich rocks from the eastern part of the Palaeo- to Mesoproterozoic Singhbhum shear zone. This is the first report of florencite from the Precambrian rocks of the Indian Shield. Host rock of florencite is a kyanite-rich rock (>80  vol%) with small and variable amounts of quartz, lazulite, augelite, and rutile. Florencite forms small (<20 microns) idioblastic-to-subhedral crystals that are included in large kyanite grains. Rarely, florencite replaces kyanite. The florencite has small proportion of crandallite (8.7–11.8 mol%) and goyazite (<2 mol%) components. Florencite of this study is dominated by Ce (~49 mol%) with significant La (~30 mol%) and Nd (~21 mol%). Compared to other florencite occurrences of the world, florencite of the studied rock is impoverished in S, Sr, and Ba and rich in P. Stability of the assemblage florencite-kyanite-augelite-lazulite and the quantitative thermobarometry in the adjoining rocks suggest that florencite was formed during Palaeoproterozoic metamorphism that culminated at the range of and  kbar. Integrating all the geological features it is postulated that florencite was formed due to metasomatism of some aluminous protolith by infiltration of acidic fluids charged with and LREE.

1. Introduction

Florencite is a rare but important mineral in the alunite super group with the general formula of AB3(XO4)2(OH)6, where A-site filled with Ce, La, and Nd, B-site with Al and X-site with P (Bayliss et al. [1]). The structure of florencite also accommodates variable amounts of Ca2+, Pb2+, Hg2+, K+, Ba2+, Sr2+, Rb+ (in A-site), Fe3+, Cu2+, Zn2+, Sn2+, V3+, Cr3+, and Ga3+ (in B-site) (Bayliss et al. [1], Dill [2]). Florencite is commonly associated in hydrothermally altered rock (Dill [2], Gaboreau et al. [3], Hikov et al. [4], and Repina [5], among others) and less commonly in metamorphic rocks (Nagy et al. [6], Izbrodin et al. [7], and Janots et al. [8]). Because of its open structure that can accommodate a large number of cations and anions including the REE, the composition of florencite provides a wealth of information about the source and composition of the metamorphic and hydrothermal fluids (Visser et al. [9], Nagy et al. [6], Dill [2], Gaboreau et al. [3], Hikov et al. [4], Izbrodin et al. [7], Repina [5], and Janots et al. [8]). Once formed florencite is very difficult to be destroyed even in the weathering profile and hence controls the mobility of LREE over a wide range of geological conditions (Gaboreau et al. [3], Izbrodin et al. [7], and Repina [5]). Florencite is associated with different types of hydrothermal or deposits including unconformity type uranium deposits and thus the presence of this mineral can be used as a pathfinder mineral in exploration of these deposits (Gaboreau et al. [3]).

Singhbhum shear zone (SSZ) of the East Indian shield separates the Palaeo- to Meso- to Neo Archaean Singhbhum craton from Palaeoproterozoic metamorphosed volcano sedimentary pile, known as North Singhbhum Fold Belt (NSFB, Figure 1 after Dunn and Dey [10] and Saha [11]). It is generally agreed upon that Palaeoproterozoic tectonism led to thrusting of the NSFB over the Archaen Singhbhum craton along the SSZ (discussed in Sarkar and Gupta [12]). Multitudes of rocks are intermingled, intensely sheared and hydrothermally altered along the SSZ. Repeated hydrothermal activities developed different types of Cu-Fe-U-P deposits that are associated with tourmalinization, muscovitization, and ferruginization (discussed in Sengupta et al. [13], and Sarkar and Gupta [12]). Infiltration-driven metamorphism in the SSZ produced a number of exotic rocks including per-aluminous kyanite-quartz rocks that fringe the northern boundary of the SSZ (Figures 1 and 2; Figure 2: partly after Mukhopadhyay and Deb [14]). In the eastern part, where the SSZ takes a bend towards south (Figure 1), kyanite-quartz rock is spatially associated with chloritoid-bearing schist, pssammopelites, mica schist, and bands of tourmalinite (Figure 2). All these rocks share a common history of deformation and metamorphism that culminated at 490 ± 40°C and 6.3 ± 1 kbar (Sengupta [15]). In this communication, we are describing the mode of occurrence of florencite in the host of kyanite-rich rock (>80 vol% kyanite) that is exposed near the village of Kanyaluka (Figure 2). Integrating all the petrological data we demonstrate that florencite was developed due to infiltration of acidic fluid charged with P and LREE into the per-aluminous kyanite-rich rock at the culmination of metamorphism and deformation. Incidentally, this is the first report of florencite from any Precambrian rocks of India.

2. Petrography and Mineral Chemistry

In domains of minimum strain, kyanite-rich rock develops randomly oriented blades of kyanite that occupy more than 80 vol% of the rock (Figure 3(a), abbreviations after Kretz [16]). Grains of quartz and rutile occupy the interstitial space of the mesh formed by the kyanite blades (Figures 3(a) and 3(b)). The kyanite-rich rock develops centimeter to decimeter thick bands of intense shearing. In the shear bands, kyanite blades are kinked, bent, and fractured (Figure 3(b)) and the quartz grains show undulose extinction. Locally, deformed kyanite blades are extensively replaced by augelite and lazulite (Figure 4(a)). Unlike kyanite, lazulite and augelite do not show any deformation (static growth). In the backscattered electron (BSE) images, florencite grains appear as numerous small bright spots in the dull background composed of lazulite, kyanite, and quartz (Figure 4(b)). Small disseminated idioblastic, subhedral to anhedral crystals (<20 microns) of florencite are included in kyanite, quartz, and lazulite (Figures 4(c) and 4(d)). Rarely, florencite replaces kyanite (Figure 4(c)). Textural features attest to the view that florencite crystals are left stranded within lazulite when the latter mineral replaced kyanite (Figure 4(d)). This feature suggests equilibrium coexistence of florencite and lazulite.

Electron microprobe analyses and WDS spectrum of the florencite are presented in Table 1 and Figure 5, respectively. Also included in Table 1 are the representative analyses of kyanite, lazulite, and rutile. For comparison, florencite analyses from some well-known localities are also included in Table 1. Chemical compositions of florencite and the adjacent minerals were determined from carbon-coated thin sections by electron microprobe analysis (EMPA) with a CAMECA SX100 electron microprobe at the Central Petrological Laboratory, Geological Survey of India, Kolkata. For elements other than Sr, Ba, and the REE, the accelerating voltage used was 15 kV with a 12 nA current. Elements were analyzed using natural standards, except for Mn and Ti for which synthetic standards were used. For the heavy metals (Ba, Sr, and REE) 20 kV and 20 nA were used. The following standards are used for REE (REE glass), Sr (celestite), and Ba (barite). The raw data were processed using the PAP procedure (Pouchou and Pichoir [17]). The composition of florencite is recalculated on 11 oxygen basis and the nomenclature of the different species is according to Bayliss et al. [1]. Compositionally florencite is essentially a solid solution of the species Florencite-(Ce) (48.7 mol%), Florencite-(La) (29.9 mol%), and Florencite-(Nd) (21.3 mol%) (Table 1). Similar to other natural florencite compositions, concentrations of LREE outweigh the concentrations of HREE. The concentrations of HREE, S, and As are below the detection limit of electron microprobe. Concentrations of Sr (0.002 to 0.008 apfu), Ba (~0.00003  apfu), Ca (0.040 to 0.062  apfu), and K (0.001 to 0.012  apfu) are low. Concentration of ThO2 varies between ~0.5 and 1.2 wt% (0.01–0.024  apfu). The WDS spectrum suggests that the elements that are not measured do not have any significant concentrations. Lazulite is dominated by Mg (98.06 mol% lazulite) with a small amount of scorzalite (1.94 mol% Fe-Lazulite, Table 1). Kyanite, rutile, and quartz have essentially the end member compositions.


ElementsLocation
Florencite (calculated on 11 oxygen basis. Values in wt%)Florencite data by Nagy et al. 2002 [6] (values in wt%)Florencite data by Janots et al. 2006 [8] (values in wt%)Florencite data by Doroshkevich et al. 2009 [19] (values in wt%)Lazulite (values in wt%)Augelite (values in wt%)Kyanite (values in wt%)Rutile (values in wt%)
Singhbhum shear zone (SSZ)Sopron Hills, Eastern Alps, HungarySebtide complex, Rif, MoroccoAmba-Dongar, Gujarat, IndiaSinghbhum shear zone (SSZ)

SiO20.00 0.06 0.01 n.a. 0.24–4.2 >0.75 0.01 0.23 36.69 0.00
TiO20.07 0.00 0.04 n.a. n.a. n.a. 0.03 0.06 0.02 100.90
Al2O328.47 27.37 27.28 28.66–31.89 27.10–31.92 27.86–30.67 33.49 49.30 62.45 0.06
Cr2O30.00 0.00 0.00 n.a. n.a. n.a. 0.00 0.08 0.04 0.13
FeO 0.00 0.01 0.00 n.a. 0.17–1.4 n.a. 0.00 0.00 0.03 0.10
MnO 0.00 0.00 0.00 n.a. n.a. n.a. 0.43 0.04 0.02 0.00
CaO 0.42 0.64 0.54 0.72–1.44 0.42–0.69 0.23–0.81 0.01 0.00 0.00 0.01
MgO 0.01 0.05 0.10 n.a. 0.02–0.70 n.a. 13.32 0.03 0.01 0.00
Na2O 0.09 0.09 0.11 n.a. 0.01–0.06 n.a. 0.03 0.00 0.06 0.00
K2O 0.00 0.00 0.01 n.a. n.a. n.a. 0.00 0.00 0.02 0.01
P2O530.81 30.72 30.84 26.97–28.93 22.4–26.4 26.08–28.56 48.44 37.09 0.00 0.00
ZrO20.00 0.00 0.00 n.a. n.a. n.a.
Nb2O50.00 0.00 0.04 n.a. n.a. n.a.
La2O36.83 7.69 7.12 6.46–8.66 4.22–4.25 3.91–12.64
Ce2O3 10.93 12.15 11.78 10.91–14.33 8.37–9.26 4.94–12.32
PbO 0.00 0.00 0.00 n.a. n.a. n.a.
ThO20.49 1.18 1.18 0.55–9.94 0.59–1.09 n.a.
U2O30.04 0.02 0.02 n.a. 0.07–0.17 n.a.
BaO 0.00 0.00 0.00 n.a. n.a. n.a.
SrO 0.12 0.15 0.10 0.16–0.67 1.32–5.91 4.47–13.36
Nd2O32.70 2.61 2.69 1.65–5.00 3.96–4.80 1.02–2.91
Sm2O31.10 1.06 1.09 0.10–0.92 0.55–0.60 n.a.
SO30.00 0.00 0.00 n.a. 0.21–0.59 1.08–4.71
Total 82.08 83.81 82.95 87.6990.36 78.2186.35 71.4078.98 95.76 86.83 99.40 101.25

a.p.f.u. a.p.f.u. a.p.f.u. a.p.f.u. a.p.f.u. a.p.f.u. a.p.f.u. a.p.f.u. a.p.f.u. a.p.f.u.
Si 0.00 0.01 0.00 n.a. 0.020–0.379 0.060–0.170 0.00 0.02 1.00 0.00
Ti 0.00 0.00 0.00 n.a. n.a. n.a. 0.00 0.00 0.00 1.00
Al 2.99 2.90 2.89 3.203–3.360 2.880–3.131 2.710–2.950 1.95 3.84 2.00 0.00
Cr 0.00 0.00 0.00 n.a. n.a. n.a. 0.01 0.00 0.00 0.00
Fe 0.00 0.00 0.00 n.a. 0.012–0.107 0.020–0.333 0.02 0.00 0.00 0.00
Mn 0.00 0.00 0.00 n.a. n.a. n.a. 0.00 0.00 0.00 0.00
Ca 0.04 0.06 0.05 0.068–0.105 0.038–0.067 0.020–0.070 0.00 0.00 0.00 0.00
Mg 0.00 0.01 0.01 n.a. 0.003–0.095 n.a. 0.98 0.00 0.00 0.00
Na 0.02 0.02 0.02 n.a. 0.002–0.012 n.a. 0.00 0.00 0.00 0.00
K 0.00 0.00 0.00 n.a. n.a. n.a. 0.00 0.00 0.00 0.00
P 2.33 2.34 2.35 2.041–2.117 1.710–1.863 1.770–2.001 2.03 2.08 0.00 0.00
Zr 0.00 0.00 0.00 n.a. n.a. n.a.
Nb 0.00 0.00 0.00 n.a. n.a. n.a.
La 0.11 0.13 0.12 0.104–0.106 0.131–0.140 0.110–0.340
Ce 0.18 0.20 0.19 0.204–0.213 0.277–0.282 0.140–0.392
Pb 0.00 0.00 0.00 n.a. n.a. n.a.
Th 0.01 0.02 0.02 n.a. 0.022–0.011 n.a.
U 0.00 0.00 0.00 n.a. 0.001–0.004 n.a.
Ba 0.00 0.00 0.00 n.a. n.a. n.a.
Sr 0.01 0.01 0.01 0.011–0.035 n.a. n.a.
Nd 0.09 0.08 0.09 0.142–0.156 0.128–0.143 0.030–0.071
Sm 0.03 0.03 0.03 0.023–0.027 0.018–0.019 n.a.
S b.d.l. b.d.l. b.d.l. n.a. 0.069–0.285 0.070–0.273
Total cation 5.80 5.80 5.79 5.8925.992 5.7635.945 5.6375.834 4.98 5.95 3.00 1.00

REE0.42 0.45 0.44 0.484–0.537 0.603–0.612 0.300–0.603
Florencite (mol%) 89.94 86.69 88.45
Goyazite (mol%) 1.36 1.47 1.03
Crandallite (mol%) 8.70 11.84 10.52

Note n.a.: not available, b.d.l.: below detection limit.

Entry of small amount of Th and Ca in the structure of florencite can be explained by the substitution (Nagy et al. [6], Georgieva and Velinova [18], and Gaboreau et al. [3]). Compared to the florencite compositions reported from many florencite occurrences in the world, florencite compositions of this study are depleted in Sr, Ca, Ba, and S whereas they are enriched in P2O5 (Table 1).

3. Discussion

Florencite in the kyanite rich rock of the Singhbhum shear zone records the first occurrence of this mineral from any Precambrian rocks of the peninsular India. The only other locality of florencite in India is the carbonatite complex of Amba Dongar, Gujarat (Doroshkevich et al. [19]).

Textural features suggest that florencite was formed during and after the growth of kyanite and, hence, originated during metamorphism that accompanied the ductile shearing of the studied rock. Florencite remained stable during the formation of lazulite and augelite that replaced kyanite under static condition (post-shearing). Experimental study in the Al-P-O-H system and the observations from natural rocks show that the assemblage augelite + kyanite is stable at conditions 380°–475°C and pressure >2 kbar (Wise and Loh [20] and Visser et al. [9]). The assemblage kyanite + lazulite, on the other hand, has a wide thermal and baric stability (>400°C and >2 kbar, Schmid-Beurmann et al. [21] and Morteani et al. [22]). Stability of florencite at high temperature (up to 550°C) is reported from the eastern Alps (Nagy et al. [6]) and from African carbonatites (Mckie [23]). Briefly, the assemblage kyanite + augelite + lazulite + florencite appears to form at temperature and pressure that exceeded 400°C and 2 kbar. This is in a good agreement with the calculated values of 490 ± 40°C and ~6 ± 1 kbar from the adjoining chloritoid garnet bearing schist (Sengupta [15]).

Origin of florencite in kyanite-quartz rock requires advective transport of LREE and P presumably by infiltration of aqueous fluids. Singhbhum shear zone is characterized by repeated infiltrations of aqueous fluids that resulted in mineralization of Cu-Fe-U-P and tourmalinization (reviewed in Sengupta et al. [13] and Sarkar and Gupta [12]). In this study we document phosphate, REE and Mg-metasomatism, which developed end member lazulite (very low content of scorzalite) in kyanite-rich rock. Several studies have demonstrated that florencite develops in hydrothermally altered (sensu lato) rock in which the metasomatic fluids are oxidized and have acidic pH (Visser et al. [9], Nagy et al. [6], Gaboreau et al. [3], Hikov et al. [4] and Georgieva and Velinova [18]). In view of this we envisage that infiltration of acidic fluid from an extraneous source to be responsible for the development of florencite. Absence of muscovitization of kyanite in kyanite quartz rock of this particular studied area and extensive tourmalinization of the adjoining rocks (Sengupta et al. [13]) supports that acidic metasomatic fluids infiltrated the rocks of the area. Studies have shown that acidic fluids can dissolve a large amount of and LREE as these chemical species form the ligand (REE ) (Ayers and Watson [24], c.f. Jones et al. [25]). This fluid upon interacting with per-aluminous host rock stabilized florencite (Nagy et al. [6]).

4. Conclusion

(1)Florencite, a REE-Al phosphate, has been reported from a metamorphosed kyanite-rich rock from the Singhbhum shear zone of the east Indian Shield.(2)Petrology of the florencite-bearing mineral association suggests metamorphic growth of florencite in the range of ~6 ± 1 kbar and 490° ± 40°C. This is the first report of florencite from Precambrian rocks of India.(3)Florencite was formed due to interaction of acidic aqueous fluids charged with PO4− and REE and aluminous country rock during regional metamorphism and ductile shearing in the Singhbhum shear zone.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

Maitrayee Chakraborty and Sayan Biswas acknowledge the research grants sanctioned by the CSIR, New Delhi, and UGC, New Delhi, respectively. Nandini Sengupta acknowledges the financial assistance from project WOS-A, DST (Department of Science and Technology, New Delhi). Pulak Sengupta acknowledges the financial assistance from the CAS, Department of Geological Sciences and UPE-II, Jadavpur University. They thank Mr. Priyadarshi Chowdhury and Dr. A. Gupta for their assistance during the fieldwork. They also thank two anonymous reviewers for their helpful comments that improved the clarity of the paper.

References

  1. P. Bayliss, U. Kolitsch, E. H. Nickel, and A. Pring, “Alunite supergroup: recommended nomenclature,” Mineralogical Magazine, vol. 74, no. 5, pp. 919–927, 2010. View at: Publisher Site | Google Scholar
  2. H. G. Dill, “The geology of Aluminium Phosphates and sulfates of the alunite supergoup,” Earth-Science Reviews, vol. 53, pp. 35–93, 2001. View at: Google Scholar
  3. S. Gaboreau, D. Beaufort, P. Vieillard, P. Patrier, and P. Bruneton, “Aluminum phosphate-sulfate minerals associated with Proterozoic unconformity-type uranium deposits in the East Alligator River Uranium Field, Northern Territories, Australia,” Canadian Mineralogist, vol. 43, no. 2, pp. 813–827, 2005. View at: Google Scholar
  4. A. Hikov, C. Lerouge, and N. Velinova, “Geochemistry of alunite group minerals in hydrothermally altered rocks from the Asarel porphyry copper deposit, Central Srednogorie,” Review of the Bulgarian Geological Society, vol. 71, no. 1–3, pp. 133–148, 2010. View at: Google Scholar
  5. S. A. Repina, “Fractionation of REE in the xenotime and florencite paragenetic association from Au-REE mineral occurrences of the Nether-Polar Urals,” Geochemistry International, vol. 49, no. 9, pp. 868–887, 2011. View at: Publisher Site | Google Scholar
  6. G. Nagy, E. Draganits, A. Demény, G. Pantó, and P. Árkai, “Genesis and transformations of monazite, florencite and rhabdophane during medium grade metamorphism: examples from the Sopron Hills, Eastern Alps,” Chemical Geology, vol. 191, no. 1–3, pp. 25–46, 2002. View at: Publisher Site | Google Scholar
  7. I. A. Izbrodin, G. S. Ripp, and A. G. Doroshkevich, “Aluminium phosphate and phosphate-sulphate minerals in kyanite schists of the Ichetuyskoye area, West Transbaikalia, Russia: crystal chemistry and evolution,” Mineralogy and Petrology, vol. 101, no. 1, pp. 81–96, 2011. View at: Publisher Site | Google Scholar
  8. E. Janots, F. Negro, F. Brunet, B. Goffé, M. Engi, and M. L. Bouybaouène, “Evolution of the REE mineralogy in HP-LT metapelites of the Sebtide complex, Rif, Morocco: monazite stability and geochronology,” Lithos, vol. 87, no. 3-4, pp. 214–234, 2006. View at: Publisher Site | Google Scholar
  9. D. Visser, R. O. Felius, and M. Moree, “Augelite and cerian crandallite in dumortierite quartzites, Vaca Morta quarry, Vereda range, Macaúbas, Bahia, Brazil,” Mineralogical Magazine, vol. 61, no. 4, pp. 607–609, 1997. View at: Google Scholar
  10. J. A. Dunn and A. K. Dey, “Geology and petrology of Eastern Singhbhum and surrounding areas,” Memoirs of the Geological Survey of India, vol. 69, no. 2, 1942. View at: Google Scholar
  11. A. K. Saha, “Crustal evolution of Singhbhum, North Orissa, Eastern India,” Geological Society of India Memoir, vol. 27, article 341, 1994. View at: Google Scholar
  12. S. C. Sarkar and A. Gupta, Crustal Evolution and Metallogeny in India, vol. 741, Cambridge University Press, 2012.
  13. N. Sengupta, P. Sengupta, and H. K. Sachan, “Aluminous and alkali-deficient tourmaline from the Singhbhum Shear Zone, East Indian shield: insight for polyphase boron infiltration during regional metamorphism,” American Mineralogist, vol. 96, no. 5-6, pp. 752–767, 2011. View at: Publisher Site | Google Scholar
  14. D. Mukhopadhyay and G. K. Deb, “Structural and textural development in Singhbhum shear zone, eastern India,” Proceedings of the Indian Academy of Sciences, vol. 104, no. 3, pp. 385–405, 1995. View at: Publisher Site | Google Scholar
  15. N. Sengupta, “Stability of chloritoid + biotite-bearing assemblages in some metapelites from the Palaeoproterozoic Singhbhum Shear Zone, eastern India and their implications,” Geological Society, London—Special Publications, vol. 365, pp. 91–116, 2012. View at: Google Scholar
  16. R. Kretz, “Symbols for rock-forming minerals,” American Mineralogist, vol. 68, no. 1-2, pp. 277–279, 1983. View at: Google Scholar
  17. J. L. Pouchou and F. Pichoir, “A new model for quantitative X-ray microanalysis—part-I: application to the analysis of homogeneous samples,” La Recherche Aérospatiale, no. 3, pp. 167–192, 1984. View at: Google Scholar
  18. S. Georgieva and N. Velinova, “Florencite-(Ce, La, Nd) from the advanced argillic alterations in the Chelopech high-sulphidation epithermal Cu-Au deposit, Bulgaria,” in Proceedings of the National Conference with International Participation (GEOSCIENCES '12), Bulgarian Geological Society, 2012. View at: Google Scholar
  19. A. G. Doroshkevich, S. G. Viladkar, G. S. Ripp, and M. V. Burtseva, “Hydrothermal REE mineralization in the Amba Dongar carbonatite complex, Gujarat, India,” Canadian Mineralogist, vol. 47, no. 5, pp. 1105–1116, 2009. View at: Publisher Site | Google Scholar
  20. W. S. Wise and S. E. Loh, “Equilibria and origin of minerals in the system Al2O-AlPO4-H2O,” American Mineralogist, vol. 61, pp. 409–413, 1976. View at: Google Scholar
  21. P. Schmid-Beurmann, G. Morteani, and L. Cemič, “Experimental determination of the upper stability of scorzalite, FeAl2[OH/PO4]2, and the occurrence of minerals with a composition intermediate between scorzalite and lazulite(ss) up to the conditions of the amphibolite facies,” Mineralogy and Petrology, vol. 61, no. 1–4, pp. 211–222, 1998. View at: Google Scholar
  22. G. Morteani, D. Ackermand, and H. A. Horn, “Aluminum-phosphates and borosilicates in muscovite-kyanite metaquartzites near Diamantina (Minas Gerais, Brazil): petrogenetic implications,” Periodico di Mineralogia, vol. 70, pp. 111–129, 2001. View at: Google Scholar
  23. D. Mckie, “Goyazite and florencite from two African carbonatites,” Mineralogical Magazine, vol. 33, pp. 281–297, 1962. View at: Google Scholar
  24. J. C. Ayers and E. B. Watson, “Solubility of apatite, monazite, zircon, and rutile in supercritical aqueous fluids with implications for subduction zone geochemistry,” Philosophical Transactions—Royal Society of London A, vol. 335, no. 1638, pp. 365–375, 1991. View at: Google Scholar
  25. A. P. Jones, F. Wall, and C. T. Williams, Eds., Rare Earth Minerals: Chemistry, Origin and Ore Deposits, vol. 357 of The Mineralogical Society Series 7, Chapman and Hall, 1996.

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