Mineralogy,paragenesis and genesis of the braunite deposits of the Mary Valley Manganese Belt,Queensland, Australia

The Mary Valley manganese deposits exhibit mineralogy and textures characteristic of at least four parageneses. The deposits consist mainly of isolated occurrences of braunite, together with a number of lower and higher valency manganese oxides, and manganese silicates, in bedded radiolarian cherts and jaspers of Permian age. The parageneses are: (a) Braunite — quartz (primary), (b) Braunite — hausmannite — spessartine — tephroite — quartz (metamorphic). (c) Hydrated manganese silicates — barite — braunite — hausmannite (hydrothermal veins), (d) Tetravalent manganese oxides (pyrolusite, cryptomelane, manjiroite, nsutite) (supergene). The primary mineralisation is interpreted as the result of the geochemical separation of Mn from Fe in a submarine exhalative system, and the precipitation of Mn as oxide within bedded radiolarian oozes and submarine lavas. During diagenesis this hydrothermal manganese oxide reacted with silica to produce primary braunite. The later geological of evolution of this volcanogenicsedimentary deposit involved metamorphism, hydrothermal veining by remobilised manganese, and supergene enrichment.     

Manganese mineralization in Archean greenstone belt,Joda–Noamundi sector,Noamundi basin,East Indian Shield

A Mesoarchean greenstone belt (3.5–3.0 Ga) in the western part of the East Indian Shield comprising the Iron Ore Group of the Noamundi basin contains economic resources of both iron and manganese ores in the NNE plunging regional synclinorium. Manganese mineralization in the central and eastern parts of this synclinorium, particularly in Joda–Noamundi sector, has taken place in multiple cycles starting from syngenetic sedimentary and exhalative type through mobilization and remobilization in different stages of tectonism, deformation and hydrothermal activities to latest lateritic or supergene type. A relatively high temperature metamorphic jacobsite–hausmannite–bixbyite–braunite assemblage, low temperature hydrothermal pyrolusite–psilomelane–hollandite assemblage and supergene pyrolusite–manganomelane–groutite–polianite assemblage are present and were formed by recycling of manganese in different stages of mineralization. A detailed structural study of the manganese ore bodies as well as their ore petrographic and mineralogical characteristics with mineral chemistry has revealed systematic mineralization and their relation to deformational phases. Such recycling of manganese and its structural control of mineralization in different phases is unique of its kind in comparison with other Archean manganese deposits in the world.     

Manganese deposits: Communication 1. Genetic models of manganese ore formation

Major regularities in the formation of manganese rocks and ores have been established on the basis of available published and original data. The proposed genetic classification of main manganese deposits (with model examples) is as follows: sedimentary-diagenetic (Nikopol, Bol’she-Tokmak; Ukraine), (volcanogenic) hydrothermal-sedimentary (deposits of the Atasui area, Kazakhstan; Magnitogorsk Trough, South Urals), epigenetic (catagenetic) (deposits of the Kalahari manganese ore field, South Africa; Usinsk deposit, Kuznetsk Alatau), and supergene (residual, infiltrational, cavern filling, and pisolitic deposits in India, Brazil, South Africa, and Australia). The results suggest the following conclusions: (1) all primary manganese rocks and ores at the known deposits are hydrothermal- and diagenetic-sedimentary formations of marine environments; (2) manganese concentrations achieve the size of deposits at postsedimentary stages of the initial manganiferous sediment and manganese rock transformation (diagenesis, catagenesis, and retrograde diagenesis); (3) indispensable participation of the isotopically light carbon dioxide related to the destruction of organic matter (OM) is a characteristic feature of manganese carbonate formation during diagenesis; and (4) the role of organic carbon in manganese ore formation becomes notable since early stages of Mn accumulation in the Precambrian sedimentary basins (terminal Archean-initial Early Proterozoic).     

鄂东北早元古代沉积变质锰矿元素矿物组合特征

鄂东北早元古代沉积变质锰矿是我国时代最古老的锰矿之一,是由早元古代锰质碳酸盐岩经区域变质作用而成,后又经风化富集形成工业矿床。由于特殊的地质构造背景和成矿作用的多阶段性,元素和矿物组合复杂,具有独特性。本文研究了各种组分的演变关系和元素集散因素,为锰质碳酸盐岩在高压绿片岩相区域动力变质及其后表生作用中的演变提供了一个实例。     

Manganese and ferromanganese ores from different tectonic settings in the NW Himalayas,Pakistan

In Pakistan manganese and ferromanganese ores have been reported from the Hazara area of North West Frontier Province, Waziristan agencies in the Federally Administered Tribal Areas and the Lasbela-Khuzdar regions of Baluchistan. This study is focused on comparison of mineralogy and geochemistry of the continental ferromanganese ores of Hazara and the ophiolitic manganese ores of the Waziristan area of Pakistan. In the Hazara area, ferromanganese ores occur at Kakul, Galdanian and Chura Gali, near Abbottabad, within the Hazira Formation of the Kalachitta-Margala thrust belt of the NW Himalayas of the Indo-Pakistan Plate. The Cambrian Hazira Formation is composed of reddish-brown ferruginous siltstone, with variable amounts of clay, shale, ferromanganese ores, phosphorite and barite. In Waziristan, manganese ores occur at Shuidar, Mohammad Khel and Saidgi, within the Waziristan ophiolite complex, on the western margin of the Indo-Pakistan Plate in NW Pakistan. These banded and massive ores are hosted by metachert and overlie metavolcanics.The ferromanganese ores of the Hazara area contain variable amount of bixbyite, partridgeite, hollandite, pyrolusite and braunite. Bixbyite and partridgeite are the dominant Mn-bearing phases. Hematite dominates in Fe-rich ores. Gangue minerals are iron-rich clay, alumino-phosphate minerals, apatite, barite and glauconite are present in variable amounts, in both Fe-rich and Mn-rich varieties. The texture of the ore phases indicates greenschist facies metamorphism. The Waziristan ores are composed of braunite, with minor pyrolusite and hollandite. Hematite occurs as an additional minor phase in the Fe-rich ores of the Shuidar area. The only silicate phase in these ores is cryptocrystalline quartz.The chemical composition of the ferromanganese ores in Hazara suggests that the Mn–Fe was contributed by both hydrogenous and hydrothermal sources, while the manganese ores of Waziristan originated only from a hydrothermal source. It is suggested that the Fe–Mn ores of the Hazara area originated from a mixed hydrothermal–hydrogenetic source in shallow water in a ontinental shelf environment due to the transgression and regression of the sea, while the Mn ores of Waziristan were formed at sea-floor spreading centers within the Neo-Tethys Ocean, and were later obducted as part of the Waziristan ophiolite complex.     

Structural controls and timing of fault-hosted manganese at Woodie Woodie,East Pilbara,Western Australia

High-grade fault-hosted manganese deposits at the Woodie Woodie Mine, East Pilbara, are predominantly hydrothermal in origin with a late supergene overprint. The dominant manganese minerals are pyrolusite, braunite, and cryptomelane. The ore bodies are located on, or near the unconformities between the Neoarchean Carawine Dolomite and the Paleoproterozoic Pinjian Chert breccia (weathering product of Carawine Dolomite), and sedimentary units of the overlying ca 1300–1100 Ma Manganese Group. Stratabound manganese is typically located above or adjacent to steep fault-hosted manganese. The ore bodies range in size from 0.2 to 5.5 Mt with an average of 0.5 Mt. Historically, over 35 Mt of manganese has been mined at Woodie Woodie, and current ore resources are 29.94 Mt at 39.94% Mn, 6.96% Fe (resource and reserves statement, June 2011, Consolidated Minerals Pty Ltd).Manganese mineralization at Woodie Woodie is related to northwest–southeast directed extension and basin formation during the Mesoproterozoic. Basin architecture is generally well preserved and major manganese occurrences are localised along growth faults which down-throw the Pinjian Chert Breccia into local extensional basins. Manganese ore bodies are typically located on steep 2nd and 3rd order structures that extend off the major growth faults. Mineralized structures display a dominant northeast-trend reflecting the direction of maximum dilation during northwest–southeast extension.A paragenetic sequence is identified for the manganese ore at Woodie Woodie, with early hydrothermal braunite–pyrolusite–cryptomelane–todorokite–hausmannite, overprinted by late supergene oxides. Preliminary fluid inclusion studies in quartz crystals intergrown with pyrolusite and cryptomelane indicate that primary and pseudosecondary inclusions display a range of salinities from 1 to 18 eq. wt.% NaCl and trapping temperatures estimated to be from 220º to 290º at 1 kbar pressure.A lead–manganese oxide (coronadite) is common in manganese ores at Woodie Woodie, and Pb-isotope studies of 40 lead-rich ore samples from 16 pits indicate mineralization occurred within an age range of 955–1100 Ma. A mixed source is suggested for the lead, but was predominantly basalts and/or volcanogenic sedimentary units (e.g., Jeerinah Formation) of the ca 2700 Ma Fortescue Group. The typically high Mn:Fe ratios and enrichment in elements such as Pb, As, Cu, Mo, Zn are consistent with a dominantly hydrothermal origin for the manganese at Woodie Woodie. Supergene manganese is distinguished from hypogene manganese by a marked enrichment in REE in the supergene manganese.An early structural framework, established during Neoarchean rifting, provides a major structural control on manganese ore distribution. The Woodie Woodie mine corridor is located in a zone of oblique strike-slip extension on major northwest-trending transform faults and north-trending oblique normal faults. A major transform structure at the southern end of the Woodie Woodie mine corridor (Jewel-Southwest Fault Zone) likely acted as a major fluid conduit for manganese-bearing hydrothermal fluids and this would account for the concentration of significant manganese ore occurrences to the north and south of this structure.     

Geology and ore genesis of the manganese ore deposits of the Postmasburg manganese-field,South Africa

The Postmasburg Mn/Fe-ores occur exclusively in dolomitic Precambrian sinkhole structures with siliceous breccias and shales as hostrocks. The main manganese minerals are braunite and bixbyite, apart from secondary alteration products of the psilomelane-manganomelane family. Various generations of ore minerals could be identified. The ore mineralization is subdivided into three different genetic types. They are classified either as pure karst deposits or as combined formations of karst origin and shallow marine sedimentation due to the transgression of the Banded Iron Formation (BIF) sea. Post-sedimentary metamorphism is identified as very low grade. The development of the different ore types is illustrated schematically.     

Mineralogy, chemistry and genesis of Nishikhal manganese ores of South Orissa, India

Manganese ores of Nishikhal occur as distinctly conformable bands in the khondalite suite of rocks belonging to the Precambrian Eastern Ghats complex of south Orissa, India. Manganese minerals recorded are cryptomelane, romanechite, pyrolusite, with minor amounts of jacobsite, hausmannite, braunite, lithiophorite, birnessite and pyrophanite. Goethite, graphite, hematite and magnetite are the other opaque minerals and quartz, orthoclase, garnet, kaolinite, apatite, collophane, fibrolite, zircon, biotite and muscovite are the gangue minerals associated with these ores. The mineral chemistry of some of the phases, as well as the modes of association of phosphorous in these ores have been established. The occurrence of well-defined bands of manganese ore; co-folding of manganese ore bands and associated metasedimentary country rocks; the min-eral assemblage of spessartite-sillimanite-braunite-jacobsite-hausmannite; the geochemical association of Mn-Ba-Co-Ni-Zn together with the Si versus Al and Na versus Mg plots of the manganese ores suggest that the Nishikhal deposit is a metamorphosed Precambrian lacustrine deposit. Continental weathering appears to be the source for manganese and iron. After deposition and probable diagenesis, the manganese-rich sediments were metamorphosed along with conformable psammitic and pelitic sediments under granulite facies conditions, and subsequently underwent supergene enrichment to produce the present deposit. Received: 14 March 1995 / Accepted: 11 April 1996     

Geological and Geochemical Investigation of Three Ophiolite‐Hosted Manganese Prospects,Southeast of Birjand,South Khorasan,East of Iran

The studied ophiolite‐hosted manganese prospects are located in southeast of Birjand, South Khorasan, in the east of Iran. The manganese ores within the ophiolitic sequence in this region occur as small discrete patches, associated with radiolarian chert and shale. Manganese ores in the host rocks are recognizable as three distinct syngenetic, diagenetic, and epigenetic features. The syngenetic manganese ores occurred as bands associated with light‐red radiolarian chert. The diagenetic Mn ores occurred as lenses accompanied by dark‐red to brown radiolarian chert. The epigenetic Mn ores occurred as veins/veinlets within the green radiolarian shale. The major manganese ore minerals are pyrolusite, braunite, bixbyite, ramsdellite, and romanechite showing replacement, colloidal, and brecciated textures. The high mean values of Mn/Fe (15.32) and Si/Al (15.65), and the low mean concentration values of trace elements, such as Cu (85.9 ppm), Ni (249.9 ppm), and Zn (149 ppm), as well as the high concentration values of Si, Fe, Mn, Ba, Zn, Sr, and As in the studied manganese ores furnished sufficient evidence to postulate that the sea‐floor Mn‐rich hydrothermal exhalatives were chiefly responsible for the ore formation, and the hydrogenous processes had negligible role in generation of the ores. The further geological and geochemical evidence also revealed that the ores deposited on the upper parts of the ophiolitic sequence by submarine exhalatives. The intense hydrothermal activities caused leaching of elements such as Mn, Fe, Si, Ba, As and Sr from the basaltic lavas (spilites). After debouching of the sea‐floor exhalatives, these elements entered the sedimentary basin. The redox conditions were responsible for separation of Fe from Mn.     

Mineral paragenesis of the Kalahari managanese field, South Africa

The mineralogy of the managanese ores of the giant Paleoproterozoic Kalahari manganese deposit of the Transvaal Supergroup has been subject of many studies and up to now 135 different ore and gangue minerals have been described, of which eight represent new mineral species. Through correlation of different mineral assemblages with specific geological events and by determining relative ages of minerals in outcrop, hand specimen and under the microscope an attempt is made in this publication to construct a paragenetic sequence for this complex mineral assemblage. Sedimentation and early diagenesis of the Hotazel Formation, composed of interbedded iron formation and braunite lutite, was followed by low-grade metamorphism and associated stratabound metasomatism. Braunite lutite of sedimentary origin, comprising 97% of the total ore reserve, is composed of braunite, hematite and kutnahorite, and abundant early diagenetic kutnahorite and manganoan calcite forming laminae and ovoids. Fluid flow during late diagenesis or lower greenschist facies metamorphism led to stratabound metasomatic oxidation of Mn-bearing carbonates to hausmannite and Mn-poor calcite. Three structurally controlled hydrothermal alteration events succeed metamorphism. These events are referred to as Wessels, Mamatwan and Smartt events. The Wessels alteration event is the oldest of the three events and it is of great economic importance because virtually all of the high-grade ore (> 42% Mn), 3% of the total ore reserve, formed during this event through alteration of carbonate-rich low-grade Mamatwan-type ore (braunite lutite) to high-grade, carbonate-poor Wessels-type manganese ore. This Wessels hydrothermal alteration event took place in the northwestern part of the Kalahari deposit, associated with a system of major north-south- and minor east-west-striking normal faults. The Mamatwan alteration event is observed throughout the Kalahari manganese deposit but alteration is very localized. Reduction halos and discolouration of braunite lutite around fracture or joint-hosted sulphide-carbonate mineralization are typical of the Mamatwan alteration event. In contrast, the Smartt alteration event is characterized by oxidation of braunite lutite and the formation of todorokite and manganomelane. Syn- and Post-Kalahari supergene alteration has taken place below the suboutcrop of the Hotazel Formation against the calcretized sediments of the Cenozoic Kalahari Formation. Cryptomelane and pyrolusite are the predominant products of surficial weathering.     

三种锰硅酸盐矿物的鉴别及其研究意义

蜡硅锰矿，粒硅锰矿，鉴别，研究意义     

广东省新榕锰矿地质特征及成因探讨

新榕锰矿是广东省重要的锰矿床 ,主矿体产于地下岩溶空洞内 ,矿石中伴生银的平均含量达 10 0×10 -6以上。锰矿石中含有少量的脆银矿、溴角银矿、含锑银黝铜矿、银金矿、单斜绿铜锌矿、黄铁矿、磁黄铁矿及重晶石等矿物。据各类岩石、矿石的矿物成分 ,以及成矿元素、稀土元素地球化学特征等方面研究 ,认为Fe、Mn成矿物质主要来源于元古宇云开群和泥盆系桂头组中的富铁锰质岩层 (锰铝榴石片岩、含锰千枚岩 ) ,部分来源于矿区北部断裂带中的热液硫化物 ,伴生元素Ag、Pb、Zn等也来源于矿区北部断裂带的热液多金属硫化物。有机质 (微生物 )可能参与了成矿物质的风化淋滤、迁移、沉淀富集等成矿作用。地下岩溶空洞是最有利的成矿场所。锰矿的成矿期为新生代。矿床成因类型属迁积_岩溶堆积型锰矿     

Mineralogy of metamorphosed manganese deposits of the South Urals

A mineralogical investigation of metamorphosed manganese rocks was carried out at ore deposits related to the Devonian volcanic complexes of the Magnitogorsk paleovolcanic belt of the South Urals. The mineralogical appearance of these rocks is determined by three consecutively formed groups of mineral assemblages: (1) assemblages occupying the main volume of orebodies and formed during low-grade regional metamorphism (T = 200−250°C, P = 2–3 kbar); (2) assemblages of segregated and metasomatic veinlets that fill the systems of late tectonic fractures; and (3) assemblages of near-surface supergene minerals. Sixty-one minerals have been identified in orebodies and crosscutting hydrothermal veinlets. The major minerals are quartz, hematite, hausmannite, braunite, tephroite, andradite, epidote, rhodonite, caryopilite, calcite, and rhodochrosite. The mineral assemblages of metamorphosed manganese rocks (metamanganolites) are characterized. Chemical compositions of braunite, epidote-group minerals, piemontite, pyroxenes, rhodonite, pyroxmangite, and winchite are considered. The bibliography on geology and mineralogy of the South Ural manganese deposits is given.     

Braunite mineralogy and paragenesis from the Kajlidongri mine,Madhya Pradesh,India

The Kajlidongri manganese deposit, Madhya Pradesh, India contains braunite belonging to at least two different parageneses, i.e. a fine-grained, metamorphic type and a younger, coarser-grained, hydrothermal type. Microanalyses of braunite from these paragenetic types indicate considerable variations in iron content from zero to 32.7% Fe₃O₃, which the writers consider is due to varying proportions of braunite I and bixbyite modules in polysomatic braunite.     

Implications of rock mineralogy and texture on the feasibility of in situ leach mining of Mn-bearing iron formations of central Minnesota,U.S.A.

The U.S. Bureau of Mines is investigating the feasibility of extracting Mn using in situ leach mining methods. Among the deposits being examined are the iron formations of the Cuyuna range, Minnesota, which contain high-tonnage, low grade deposits of manganese oxides. Manganese minerals identified include pyrolusite, cryptomelane-hollandite, manganite, braunite and lithiophorite. Ore reactivities, as measured by batch leaching tests using aqueous SO₂, are compared to theoretical estimates of the leaching behavior of individual manganese minerals based on kinetic and thermodynamic evaluations. Experimental results in some cases show opposite trends to those predicted by theoretical estimates. In batch leaching tests of Cuyuna Range ores, texture was shown to be of greater importance, than thermodynamic reactivity in determining amenability to leaching. Predicting the practical potential for recovery of Mn by in situ leaching must involve identification of the effects of texture (massive, fractured-host, or interstitial) in addition to ore mineral reactivity.     

Oxidation of As^Ⅲ by Several Manganese Oxide Minerals in Absence and Presence of Goethite

Oxidation of As^Ⅲ by three types of manganese oxide minerals affected by goethite was investigated by chemical analysis, equilibrium redox, X-ray diffraction （XRD） and transmission electron microscopy （TEM）. Three synthesized Mn oxide minerals of different types, birnessite, todorokite, and hausmannite, could actively oxidize As^Ⅲ to Asv, and greatly varied in their oxidation ability. Layer structured birnessite exhibited the highest capacity of As^Ⅲ oxidation, followed by the tunnel structured todorokite. Lower oxide hansmannite possessed much low capacity of As^Ⅲ oxidation, and released more Mn^2＋ than birnessite and todorokite during the oxidation. The maximum amount of Asv produced during the oxidation of As^Ⅲ by Mn oxide minerals was in the order： birnessite （480.4 mmol/kg） 〉 todorokite （279.6 mmol/kg） 〉 hansmannite （117.9 mmol/kg）. The oxidation capacity of the Mn oxide minerals was found to be relative to the composition, crystallinity, and surface properties. In the presence of goethite oxidation of As^Ⅲ by Mn oxide minerals increased, with maximum amounts of Asv being 651.0 mmol/kg for birnessite, 332.3 mmol/kg for todorokite and 159.4 mmol/kg for hansmannite. Goethite promoted As^Ⅲ oxidation on the surface of Mn oxide minerals through adsorption of the Asv produced, incurring the decrease of Asv concentration in solutions. Thus, the combined effects of the oxidation （by Mn oxide minerals）-adsorption （by goethite） lead to rapid oxidation and immobilization of As in soils and sediments and alleviation of the As^Ⅲ toxicity in the environments.     

Oxidation and Mineralization of Mn2+ Ions Mediated by Pseudomonas putida: Insights from an Experimental Study

The formation of manganese oxides in nature is commonly mediated by microorganisms.In this study,the mineralization of biogenic manganese oxidation mediated by Pseudomanas putida has been experimentally investigated by employing various characterization techniques,including SEM,FESEM,TEM,XRD,and STXM-NEXAFS.The results indicate that Mn~(2+) ions can be oxidized into Mn(Ⅳ) minerals(birnessite and pyrolusite) and Mn(Ⅲ) minerals(hausmannite and feitknechtite),successively.The primary products(birnessite and pyrolusite) further transformed into hausmannite and feitknechtite under Mn~(2+) ion-enriched conditions.However,birnessite and pyrolusite are the endproducts of the continuous microbial oxidation processes.These biogenic Mn oxides are poorly crystallized,which provides them with a high potential for usage in environmental restoration of contaminated soils and waters contaminated with heavy metals.The approaches employed in this study will also enrich genesis research of biological oxidation of Mn(Ⅱ) species in nature.     

Sorption of ferric iron from ferrioxamine B to synthetic and biogenic layer type manganese oxides

Siderophores are biogenic chelating agents produced in terrestrial and marine environments that increase the bioavailability of ferric iron. Recent work has suggested that both aqueous and solid-phase Mn(III) may affect siderophore-mediated iron transport, but scant information appears to be available about the potential roles of layer type manganese oxides, which are relatively abundant in soils and the oligotrophic marine water column. To probe the effects of layer type manganese oxides on the stability of aqueous Fe-siderophore complexes, we studied the sorption of ferrioxamine B [Fe(III)HDFOB⁺, an Fe(III) chelate of the trihydroxamate siderophore desferrioxamine B (DFOB)] to two synthetic birnessites [layer type Mn(III,IV) oxides] and a biogenic birnessite produced by Pseudomonas putida GB-1. We found that all of these predominantly Mn(IV) oxides greatly reduced the aqueous concentration of Fe(III)HDFOB⁺ at pH 8. Analysis of Fe K-edge EXAFS spectra indicated that a dominant fraction of Fe(III) associated with the Mn(IV) oxides is not complexed by DFOB as in solution, but instead Fe(III) is specifically adsorbed to the mineral structure at multiple sites, thus indicating that the Mn(IV) oxides displaced Fe(III) from the siderophore complex. These results indicate that layer type manganese oxides, including biogenic minerals, may sequester iron from soluble ferric complexes. We conclude that the sorption of iron-siderophore complexes may play a significant role in the bioavailability and biogeochemical cycling of iron in marine and terrestrial environments.     

Models of rock varnish formation constrained by high resolution transmission electron microscopy

Nanometre-scale transmission electron microscope imagery of manganiferous rock varnishes from Death Valley, California, Peru, Antarctica, and Hawaii confirms prior infrared mineralogy studies. The building blocks of rock varnish are clay minerals that are cemented to the rock by oxyhydroxides of manganese and iron. Rock varnish is layered on the scale of nanometres, with the basic structure defined by the subparallel alignment of detrital clay minerals. Although only a few examples of bacteria were found, possible cell-wall encrustations are ubiquitous and aligned with the clay minerals. Mn–Fe oxides appear to be mobilized from bacterial casts and then reprecipitate on clay minerals that weather into monolayers. These observations have implications for varnish dating and palaeoenvironmental techniques: K–Ar and uranium-series dating of rock-varnish oxides can only yield minimum ages; however, this small spatial scale of mobilization would not alter the signal from micron-scale microchemical laminations.     

Mineralogy,geochemistry and origin of Mn in the high-Mn iron ores,Bahariya Oasis,Egypt

Although Mn is one of the major impurities in the economic iron ores from the Bahariya Oasis, information on its modes of occurrence and origin is lacking in previous studies. High-Mn iron ores from El Gedida and Ghorabi–Nasser iron mines were subjected to detailed mineralogical, geochemical, and petrographic investigations using X-ray diffraction (XRD), infrared absorption spectrometry (IR), Raman spectroscopy, X-ray fluorescence (XRF), scanning electron microscopy (SEM), and electron probe microanalyzer (EPMA) to clarify the modes of occurrence of Mn in these deposits and its origin. The results showed that the MnO₂ contents range between 0.03 and 13.9 wt.%. Three mineralogical types have been identified for the Mn in the high-Mn iron ores, including: (1) inclusions within the hematite and goethite and/or Mn accumulated on their active surfaces, (2) coarse-grained and crystalline pyrolusite, and (3) fine-grained cement-like Mn oxide and hydroxide minerals (bixbyite, cryptomelane, aurorite, romanechite, manjiroite, and pyrochroite) between the Fe-bearing minerals. The Mn carbonate mineral (rhodochrosite) was detected only in the Ghorabi–Nasser high-Mn iron ores. Since IR patterns of low-Mn and high-Mn samples are almost the same, a combination of XRD analysis using non-filtered Fe-Kα radiations and Raman spectroscopy could be the best way to identify and distinguish between different Mn minerals.Assuming that both Fe and Mn were derived from the same source, the occurrence of high-Mn iron ores at the base of the stratigraphic section of the deposits overlain by the low-Mn iron ores indicated a supergene origin of the studied ores by descending solutions. The predominance of Mn oxide and hydroxide minerals in botryoidal shapes supports this interpretation. The small grain size of Mn-bearing minerals as well as the features of microbial fossils such as spherical, elliptical, and filamentous shapes of the Fe-bearing minerals suggested a microbial origin of studied iron ores.Variations in the distribution and mineralogy types of Mn in the iron ores of the Bahariya Oasis demanded detailed mineralogical and petrographic characterizations of the deposits before the beneficiation of high-Mn iron ores from the Bahariya Oasis as feedstock for the ironmaking industries in Egypt by magnetizing reduction. High Mn contents, especially in the Ghorabi–Nasser iron ore and occurrence of Mn as inclusions and/or accumulated on the surface of the Fe-bearing minerals would suggest a possible utilization of the high-Mn iron ores to produce ferromanganese alloys.