Main minerals of abnormally high-grade ores of the Tomtor deposit (Arctic Siberia)

The Tomtor massif of Paleozoic ultramafic alkaline rocks and carbonatites is located in the northern part of the Sakha Republic (Yakutia). The massif (its total area is ~ 250 km²) is ~ 20 km in diameter, with a rounded shape and a concentrically zoned structure. The core of the massif consists of carbonatites surrounded by a discontinuous ring of ultramafic rocks and foidolites. The outer part is composed of alkali and nepheline syenites. All rocks are weathered and covered with eluvium, which is the thickest after carbonatites enriched in phosphates and REE. The weathering profile consists of four layers, from the top: kaolinite-crandallite, siderite, goethite, and francolite. The highest-grade ores are observed in the bedded deposit which fills depressions in “sagging” eluvium. The ores are laminated and cryptogranular, with high Nb, Y, Sc, and REE contents (on average, 4.5% Nb₂O₅, 7-10% REE₂O₃, 0.75% Y₂O₃, and 0.06% Sc₂O₃). The highest-grade ores are natural Nb and REE concentrates. The total REE content in some layers is > 10%. The morphologic features of the highest-grade phosphate ores from the northern part of the Burannyi site were studied. The ore-forming minerals belong to the pyrochlore group, crandallite group (goyazite), and monazite-Ce. The pyrochlore group minerals occur mainly as crystals that were completely replaced by barium-strontium pyrochlore and/or plumbopyrochlore but retained the original faces; also, they occur as numerous conchoidal fragments. The grains of the pyrochlore group minerals sometimes have a zonal structure, with an unaltered pyrochlore core and a reaction rim. Goyazite occurs predominantly as colloform grains. According to SEM and TEM data, monazite occurs in the ores as ~ 50 nm particles, which cover the outer part of halloysite tubes (800–3000 nm long and 300 nm in diameter) as a dense layer and make up peculiar biomorphic aggregates. The mineralogical data, the occurrence of biomorphic aggregates, and the close association of organic remains with ore minerals suggest that the high-grade ores of the Tomtor deposit, including the Burannyi site, resulted from a hydrothermal-sedimentary process with a presumably important role of bioaccumulation of REE phosphates.     

Geochemistry of Cadmium in Mesozoic Phosphorites of the East European Platform

Cadmium is the most toxic admixture in mineral fertilizers. The Cd concentration in Mesozoic phosphorites, which are widespread in the East European Platform, has not been investigated. The present study was stimulated by the scanty and contradictory nature of the published data on this issue. We determined Cd concentration in 21 phosphorite samples from major deposits and checked the reliability of obtained results by external replicate analyses. It has been established that the Cd concentration in phosphorites varies from 5 ppm in the Late Jurassic–Early Cretaceous basin to 2 ppm in the Late Cretaceous basin. Cadmium does not enter the structure of phosphate and sulfide minerals. The Cd concentration is independent of the phosphorus abundance. However, all studied samples show a positive correlation of Cd with organic matter mainly contained in phosphates, supporting the biophilic nature of Cd. Mesozoic phosphorites of the East European Platform accumulated in epicontinental basins. They are significantly depleted in Cd relative to Mesozoic–Cenozoic phosphorites in pericontinental basins of the southern margin of the Tethys Ocean. The Cd concentration is more stable in Mesozoic phosphorites than in Mesozoic–Cenozoic deposits.     

Structural CO2 in the Apatite of the Late Cretaceous Phosphorite Resources in Egypt: Effect on the Crystal Chemistry and Geologic Implications

Abstract: Phosphorite deposits in Egypt, known as the Duwi Formation, are a part of the Middle East to North Africa phospho‐genic province of late Cretaceous to Paleogene age. Based on the petrographical observation, the phosphatic grains in the phosphorites are classified into phosphatic mudclasts and phosphatic bioclasts. Both of them are composed of francolite. The structural CO₂ contents in the francolite range from 3.3 to 7.2 % with an average of 5.3 %. Results indicated that the substitution with CO₃^2‐ of PO₄^3‐ in the francolite decreases the unit cell volume and a‐cell dimension, and increases the c/a ratio. Effect is more obvious in the a‐cell dimension; therefore, it is more significant in distinction between the different apatite species. Lack of covariance between structural CO₂ contents in the francolite and the carbonate minerals contents may render the supposition that the phosphorites formed as a result of replacement of preexisting calcareous sediments is doubtful. Similarity in CO₂ content in both weathered and fresh samples indicates that the structural CO₂ content in the phosphorites is not affected by weathering, and reflects the conditions and CO₂ concentration of the depositional environment. Similarity in mineralogy and CO₂ contents in the different phosphatic grains and higher CO₂ content in the Egyptian phosphorites compared with the authigenic phosphates of Peru margin, which formed by the same mechanism as the Duwi phosphorites, suggest that the phosphatic grains in the Duwi Formation were francolitized during diagenesis by introducing CO₂ from the surrounding pore water and diagenesis took place at an elevated temperature. Scattered values of structural CO₂ contents suggest the reworking origin of the phosphatic grains in the late Cretaceous phosphorites in Egypt.     

沉积磷块岩结构类型、成因及成矿阶段

磷块岩的岩石类型和成矿阶段划分是磷块岩研究的一项基础性工作,早在50年代后期,叶连俊等人就对磷块岩及其分类进行过研究[1],随着沉积学的发展,尤其是近年来碳酸盐岩研究的进展,磷块岩岩石学研究也有了一些新的突破。磷块岩分类从矿体形态(层状、透镜状、结核状)、大地构造(地台型、地槽型)等分类走向了结构成因分类。在这方面,工作较多,较系统的有美国的S.R.Riggs和法国的M.S1ansky[9][10]。我国的孙枢、陈其英、赵东旭[2][3]及孟祥化[4]、周茂基[5]、东野[6]等人也先后对磷块岩的结构成因类型进行过研究。这些研究给磷块岩的分类奠定了一个很好的基础。     

Ultra-fine structures and genesis of the Campanian Negev high-grade phosphorites (southern Israel)

Ultra-fine structures of the Negev high-grade phosphorites provide valuable clues to unravelling the genesis of these rocks, the question of their differential areal distribution, and the biosedimentary mechanisms involved in their considerable enrichment. Peculiar to these phosphorites is an intergranular phosphate matrix, for the most part constituted by a variety of phosphatic microbial tubules displaying a range of spatial micro-organizations. The phosphate particles fixed by this filamentous meshwork also consists of internally organized and non-organized packed microbial remains of different types. Analogies between the fabrics of the matrix and the corpuscles lead to conception of a two-stage depositional scheme for these phosphorites, based on rhythmical repetition of two sedimentary mini-events, in a slightly oscillating, very shallow marine system—(1) a low-energy event of microbial colonization of the Mishash bottoms, followed by early phosphatization of the organic structures mainly in marginal situations; and (2) a higher-energy event which broke up the phosphatic mats into debris, redepositing them as clastic layers in nearby basinward sites, while becoming bound by a new meshwork of filamentous microphytes. The differential phosphatization of the intergranular microbial binder, again occurring mostly in marginal localities, produced highly enriched phosphorites. Minor truncations and redepositions leading to amalgamation of the successive layers account for the massive fabric now displayed by most of these rocks. Examining the structural and textural features, the validity of the sedimentary mechanisms of Recent phosphorite formation for the Campanian Negev rocks is discussed.     

朝阳磷矿磷块岩的类型和成因特征

朝阳磷矿的磷块岩有五种类型,即泥晶磷块岩、球粒磷块岩、鲕粒磷块岩、内碎屑磷块岩和细晶磷块岩。其中内碎屑磷块岩占优势。磷酸盐岩沉积在海退旋回中,是处于深水向浅水过渡的层位。磷块岩的沉积环境主要是隆起附近的浅水带。     

Trace elements in supergene phosphorites

Supergene phosphorites were analyzed for Sr, Ba, Zn, Cd, Sc, Cr, Ag, and V, i.e., elements incorporated in carbonate-apatite by isomorphic substitution. The phosphorites were subdivided into four groups: (1) phosphorites related to the weathering of sedimentary rocks, (2) phosphorites related to the weathering of endogenous rocks, (3) lacustrine coprolite phosphorites, and (4) phosphorites of ocean islands. In all the phosphorites groups, Sr, Zn, and Ba were the most abundant of the trace elements, whereas Cd, Ag, and Sc showed the lowest concentrations. Variations in trace element contents between supergene phosphorites of different genetic groups or within a single group can be explained by the different compositions of weathered rocks and geochemical environments of supergene phosphorite formation. At the same time, the contents of some trace elements are correlated with the structural type of phosphorite. In particular, phosphorite crusts or only their outer parts show elevated contents of chalcophile elements (Cd, Zn, and Ag), whereas massive phosphorites and inner parts of crusts are often enriched in such lithophile elements as Sc, V, and Cr. It was found that Cd, Zn, Ag, Sr, and Ba are positively correlated with CO₂ but show negligible correlations with other constituents of carbonate-apatite.     

Uranium in supergene phosphorites

The distribution of uranium was studied in supergene phosphorites from the zones of the weathering of sedimentary and endogenous rocks, as well as in nonmarine coprolitic phosphorites and, to a lesser extent, phosphorites from ocean islands. These phosphorites show a diversity of the composition of their carbonate-apatite and structural characteristics. The uranium content ranges mostly from 5 to 100 ppm, with minimum and maximum values of 0.5 and 790 ppm. There is no correlation between the uranium content of a phosphorite and the type of rock with which it is connected. Lacustrine coprolitic phosphorites show elevated uranium contents (about 200 ppm). The maximum uranium content was detected in finely laminated phosphorite encrustations. The correlation analysis of the whole data set (63 samples) showed that uranium content is not correlated with any other component of phosphorites at a confidence level of 0.95. In contrast, there is a correlation between U and P₂O₅, CaO, and F for the combined set of samples from southern Siberian deposits. The significant correlation of U with Na₂O and CO₂ is variable both for southern Siberia on the whole and for particular deposits from this region.     

Combustion metamorphism of bituminous sediments and the formation of melts of granitic and sedimentary composition

During combustion metamorphism, i.e. the heating of sediments rich in organic matter by spontaneous subsurface combustion, temperatures obtained are frequently high enough to cause partial or total melting of the original rocks. These melts are of particular geochemical interest because at lower temperatures their composition closely simulates that of granitic and at higher temperatures that of common sedimentary rocks. At the California localities, studied here, the parent rocks are mainly bituminous mudstones with smaller amounts of diatomites and phosphorites and lesser dolomites, limestones, shales and cherts. It is estimated that rock melting started below 1000° C. The first partial melts correspond to a melt fraction of about 5% have a constant composition which is controlled by the eutectic of the dominant mudstones, and are undistinguishable in major and trace element composition from common S-type granites. Compared with the original rocks, these melts are enriched in SiO₂, Al₂O₃, K₂O, Na₂O, as well as in Ta, Hf, Zr, Th and REE, and are depleted in all other elements studied. The only difference between these low-temperature melts and granitic ones is their oxygen isotope composition, which is that of the sedimentary parent rocks. These melts intruded the country rocks as sills and dikes and cooled to glassy rocks simulating obsidians.As temperatures rose, the melts changed composition and left the magmatic field. At the highest temperatures (in excess of 1650 C), their composition equals that of the original sediments from which they are derived, except for volatile components such as H₂O and CO₂. These melts formed intrusive bodies, mainly stocks, up to several kilometers across. On cooling, these melts formed fine-grained but holocrystalline rocks, the dominant minerals of which are cristobalite, α- and β-tridymite, calcic plagioclase, cordierite, wollastonite, gehlenite, andradite and apatite. Where the parent rocks included phosphorites, two immiscible melts formed an emulsion in which droplets of apatitic composition are surrounded by a silicate melt, almost devoid of P₂O₅.     

New occurrence of potential phosphate resource in northeast Jordan

An exploration program aided by field investigation, exploration drilling, detailed sampling, lithological and petrological studies, geochemical investigation, and resource calculation leads to the discovery of a potential phosphate resource in northeast Jordan close to the international border with Saudi Arabia and Iraq. The studied phosphate is of the Middle Eocene age that belongs to the Wadi Shallala Formation. It is equivalent to the phosphate deposits recorded in the lower part of the Umm Wual Formation in the Turayf region of Saudi Arabia and the Eocene Ratga Formation in the Ethna phosphate deposit west of Iraq. The phosphorites in the region are broadly similar in mineralogical composition and geochemical affinities. X-ray diffraction indicates the presence of francolite with variable amounts of calcite and quartz. Most samples consist of phosphate clasts embedded in carbonate and silica matrix and cement. P₂O₅ content is up to 32.3 % with an average equal to 18.6 %. The impurity is caused by the presence of variable amounts of SiO₂ and CaO. The F% and F/P₂O₅ ratio in studied phosphates is lower compared with that in phosphates from Jordan and Saudi Arabia. The geological and geochemical results were integrated for resource estimation. Three high-grade phosphate layers with ≥23 % P₂O₅ were considered in the calculations. The phosphate resource is classified as an inferred resource. The total volume of the resource is about 649 million tons. The average P₂O₅ content is 24.57, and the stripping ratio is 1:5.8.     

Organic Gases in Fluid Inclusions of Ore Minerals and Their Constraints on Ore Genesis: A Case Study of the Changkeng Au-Ag Deposit, Guangdong, China

The newly discovered Changkeng Au-Ag deposit is a new type of sediment-hosted precious metal deposit. Most of the previous researchers believed that the deposit was formed by meteoric water convection. By using a high vacuum quadrupole gas mass spectrometric system, nine light hydrocarbons have been recognized in the fluid inclusions in ore minerals collected from the Changkeng deposit. The hydrocarbons are composed mainly of saturated alkanes C1-4 and unsaturated alkenes C2-4 and aromatic hydrocarbons, in which the alkanes are predominant, while the contents of alkenes and aromatic hydrocarbons are very low. The Σalka/Σalke ratio of most samples is higher than 100, suggesting that those hydrocarbons are mainly generated by pyrolysis of kerogens in sedimentary rocks caused by water-rock interactions at medium-low temperatures, and the metallogenic processes might have not been affected by magmatic activity. A thermodynamic calculation shows that the light hydrocarbons have reached chemical equilibrium     

Phosphate-rich sedimentary rocks: Significance for organic facies and petroleum exploration

Phosphorus-bearing rocks and sediments can be divided into two genetically distinct classes: phosphatic shales or limestones and phosphorites. Phosphatic shales are primary sediments in which phosphate nodules or micronodules have formed diagenetically by precipitation of calcium phosphates derived mainly from organic phosphorus. The nodules form in reducing environments at shallow depths within the sediments, where loss of phosphate by diffusion to the overlying water column is minimized. Highly biogenic sediments containing large amounts of organic matter and some fine clastic debris provide ideal environments for the formation of phosphate nodules.Phosphorites, in contrast, represent concentrated accumulations of reworked phosphate nodules which originated in phosphatic shales or limestones. Currents, wave action, recrystallization, and erosion and resedimentation are important mechanisms in the concentration process.Phosphatic shales and limestones may become excellent oil source rocks if thermal maturity is achieved. They are useful facies indicators for anoxic or nearly anoxic depositional environments, and are often associated with restricted basins, or, during certain geologic periods, with broad shelves developed during transgressions. Phosphorites, in contrast, are often correlated with sea-level regressions or uplifts. They are modest source rocks because of their low organic carbon contents and the fact that they were reworked under oxidizing conditions. Nevertheless, because phosphorites are derived from, and often grade into, phosphatic shales, they also are of potential utility in the search for oil source beds.     

Grain size and geochemistry of surface sediments in northwestern continental shelf of the South China Sea

Eighty-six surface sediments collected from the northwestern continental shelf of the South China Sea (SCS) were analyzed for grain size distribution, calcium carbonate, organic carbon, and major and trace element compositions to investigate sediment provenance and factors controlling their geochemical composition. Sediments from the eastern continental shelf of Hainan Island have higher sand and lower clay content, while the samples from the nearshore Hainan Island have higher contents of gravel and clay. Calcium carbonate contents in samples show a positive correlation with water depth in northwestern shelf of SCS, suggesting that it is related to biological factors. However, the nearshore sediments have higher contents of organic carbon compared to those of the outer shelf, possibly suggesting that the terrigenous organic matter usually deposited in nearshore environments such as bays and estuaries. Compared with the upper continental crust, the samples have relatively lower contents of SiO₂ and Al₂O₃, higher than those of the Pearl and Red river sediments. The low contents of K₂O and Na₂O in sediments from the northwestern continental shelf are consistent with intense chemical weathering in the river basin due to the seasonally hot and humid climate regime. The sediments mainly consist of three components, including the gravel fraction composed of calcareous debris, the sand fraction composed of quartz, and the silt and clay fractions mainly composed of clay minerals. The content of each component depends on grain size, sediment source, biogenesis, and hydrodynamic conditions, which finally controls the chemical composition of the sediments. The distributions of Co/Al₂O₃, Cr/Al₂O₃, and Zr/Sc ratios for sediments in the northwestern continental shelf suggest that source rocks are mainly composed of felsic rocks rather than mafic rocks. There is a distinct difference in sediment source between eastern and western shelf sediments; the eastern shelf sediments are characterized by high Zr/Sc ratios mainly derived from the Pearl River, while the western shelf sediments have relatively low values of Zr/Sc indicating a main contribution possibly sourced from the Red River Basin. Terrigenous materials from Hainan Island usually influence the geochemistry of sediments deposited in the nearshore area.     

Lower Eocene phosphorites of the western desert,Iraq

Marine sedimentary phosphorites of Eocene age (Upper Ypresian) are exposed in the extreme west of Iraq within the Dammam Formation. They are associated with limestone and chert, and their deposition seems to have taken place in a shallow marine environment within a structurally controlled basin open to the sea from the northern and western sides only.The studied phosphorites are granular in texture, coarse-grained and cemented by calcite which is occasionally silicified. Bone fragments are present in small amounts. Carbonate-fluorapatite is the only phosphate mineral detected in these phosphorites, with relatively high amounts of the components SO₄^?2, CO₃^?2, F^?1, H₃O¹ and Na¹ substituting in the crystal structure.The Lower Eocene phosphorites of Iraq are part of the Tethyan phosphorite province, and are comparable in many aspects with those of Paleocene and Upper Cretaceous age in the Western Desert of the country.     

The incorporation of uranium into diagenetic phosphorite

The behavior of U during the diagenetic formation of marine phosphorite has been modelled. The model examines a dissolution-reprecipitation replacement of skeletal hydroxyapatite, calcium carbonate and earlier generated francolite by francolite. The amount of organic matter consumed relative to the mass of francolite formed, the replacement reaction progress, and the concentration of U in the replaced phases are the important parameters which dictate the concentration of U in the phosphate rock.A partition coefficient between apatite and interstitial solution was calculated, and is $\text{λ}{}_{\mathrm{U}}{}^{\mathrm{F}}\text{= 0.57}$.Natural phosphorites have been examined and are discussed in the light of the proposed model. The U mass-balance in a Recent phosphorite is in good accord with theoretical predictions. Differences in U concentrations between sea-floor phosphorites are explained either by the (original) variation in the organic matter distribution in the corresponding sediments and/or by mineralogical differences (CaCO₃vs. hydroxyapatite) therein.Senonian phosphate rocks which were formed via the francolite → francolite transformation, demonstrate that during that process the organic matter content in the sediment was approximately 50%.The model supports the idea that phosphorite rock formation is a multistage process.     

The use of three physico-chemical methods in the study of the organic matter associated with the sedimentary phosphorites in Djebel Onk Basin, Algeria

The study of the organic matter (OM) associated with the phosphate ore of Kef Essennoun deposit (Djebel Onk mining basin, Algeria) was with a view to determine the decomposition degree of the OM within the pellets and the matrix, and the conditions of diagenesis. The sedimentary phosphates of this deposit are constituted of sub-rounded, phosphate-rich grains (pellets) dispersed in a surrounding, much poorer than pellets in P, matrix (or gangue). The survey of the OM associated with both pellets and matrix used several types of analyses: scanning electron microscopy (SEM), scanning electron microscope with energy-dispersive X-ray analysis, Fourier transform infrared spectroscopy and nuclear magnetic resonance spectroscopy. The results show the OM, dispersed approximately homogeneously, in the form of large flat particles, within the gangue and within the phosphatic pellets in the form of small particles. The O/C ratio showed that the OM is more oxidised in the matrix than within the pellets. The oxidation increased with the phosphatisation rate of the pellets and more with the carbonation rate of the matrix, but it decreased with the silicification degree in the siliceous carbonated matrix. Two major functional classes were distinguished within pellets: aliphatic and oxygenated ones, the latter being fundamentally present in humic OM. The presence and abundance of these humic compounds in pelletal phosphorites are known from the 1980s and considered as witnessing a formation of apatite in a strictly closed environment, inside the pellet.     

Two‐Stage Sulfide Mineral Assemblages in the Mineralized Ultramafic Rocks of the Laowangzhai Gold Deposit (Yunnan,SW China): Implications for Metallogenic Evolution

The Laowangzhai gold deposit, located in the Ailaoshan gold belt (SW China), is hosted in various types of rocks, including in quartz porphyry, carbonaceous slate, meta‐sandstone, lamprophyre, and altered ultramafic rocks. In contrast to other wall rocks, the orebodies in altered ultramafic rocks are characterized by the occurrence of a large amount of Ni‐bearing minerals. The ore‐forming process of the orebodies hosted by altered ultramafic rocks can be divided into two stages: pyrite‐vaesite‐native gold and gersdorffite‐violarite stages. The contents of As and Sb increased during the evolution of ore‐forming fluid based on the mineral assemblages. Thermodynamic modeling of the Ni‐Cu‐As‐Fe‐S system using the SUPCRT92 software package with the updated database of slop16.dat indicates the fS₂ in ore‐forming fluid decreases significantly from stage I to stage II. The decreases of fS₂ due to crystallization of sulfides and fO₂ due to fluid–rock reaction were responsible for ore formation in altered ultramafic rocks of the Laowangzhai gold deposit. Geological evidence, the in situ sulfur isotope values of pyrite, and the other published isotopic data suggest that the ore‐forming fluid for ultramafic rock ores was dominantly composed of evolved magmatic fluid with the important input of sediments.     

Geochemical and Sr–Pb–Nd isotopic characteristics of the Shakhtama porphyry Mo–Cu system (Eastern Transbaikalia,Russia)

The Shakhtama Mo–Cu porphyry deposit is located within the eastern segment of the Central Asian Orogenic Belt, bordering the southern margin of the Mongol–Okhotsk suture zone. The deposit includes rocks of two magmatic complexes: the precursor plutonic (J₂) and ore-bearing porphyry (J₃) complexes. The plutonic complex was emplaced at the final stages of the collisional regime in the region; the formation of the porphyry complex may have overlapped with a transition to extension. The Shakhtama rocks are predominantly metaluminous, I-type high K calc-alkaline to shoshonitic in composition, with relatively high Mg#, Ni, Cr and V. They are characterized by crustal-like I_Sr (0.70741–0.70782), relatively radiogenic Pb isotopic compositions, ε_Nd(T) values close to CHUR (−2.7 to +2.1) and Nd model ages from 0.8 to 1.2 Ga. Both complexes are composed of rocks with K-adakitic features and rocks without adakite trace element signatures. The regional geological setting together with geochemical and isotopic data indicate that both juvenile and old continental crust contributed to their origin. High-Mg# K-adakitic Shakhtama magmas were most likely generated by partial melting of thickened lower crust during delamination and interaction with mantle material, while magmas lacking adakite-like signatures were probably generated at shallower levels of lower crust. The derivation of melts, related to the formation of plutonic and porphyry complexes involved variable amounts of old Precambrian lower crust and juvenile Phanerozoic crust. Isotopic data imply stronger contribution of juvenile mantle-derived material to the fertile magmas of the porphyry complex. Juvenile crust is proposed as an important source of fluids and metals for the Shakhtama ore-magmatic system.     

Precambrian phosphorites in the Bijawar rocks of Hirapur-Bassia areas,sagar district,madhya pradesh,India

The Precambrian phosphorites of Bijawar Group of rocks show characteristics of a epicontinental sea with restricted and very shallow marine environment of formation along some shoals, which existed during the iron-rich Precambrian times. These phosphorite deposits located in the Hirapur-Bassia areas show extensive leaching of carbonate and phosphate minerals during episodes of weathering. X-ray diffraction studies indicated that carbonate-flourapatite is the major apatitic phase in these phosphorites while crandallite developed on the surface outcrops. There is a general tendency for the depletion of CO₂ in these apatites leading to formation of flourapatite. This CO₂ is an indicator of hidden weathering in the rocks. Major and trace element determinations of phosphorite have been used to indicate various correlation factors responsible for the concentration of elements in these Precambrian leached phosphorites.The paper is a contribution to the aims and objectives of IGCP Project 156The paper is dedicated to Prof. Dr. R. C. Misra, who as a teacher and guide had been a source of inspiration to the senior author for the last two decades