Rare earth element abundances in rocks and minerals from the Fiskenaesset Complex,West Greenland

Rare earth element (REE) abundances determined by activation analysis in rocks, plagioclase and mafic separates from the Fiskenaesset Complex are presented together with data on major and trace elements in the minerals. The REE data for the rocks and plagioclases are distinct from those of many other anorthositic complexes and the abundances are some of the lowest recorded for plagioclase from terrestrial anorthosites. The bulk and trace element compositions of the Fiskenaesset plagioclases show a number of similarities to those of lunar plagioclases. The plagioclases show a positive Eu anomaly of about 10 and a depletion in the heavy REE relative to the light ones. The mafic separates are enriched in the heavy REE relative to the light ones, and show no Eu anomaly except in one sample with a positive anomaly not attributable to plagioclase contamination. It is estimated, from experimental partition coefficient data, that the REE pattern in the magma at an early stage of fractionation was La (17×) to Lu (0.7× chondrites) with a possible positive Eu anomaly. This highly fractionated REE pattern may be attributed to partial melting of a garnet-bearing source.     

Rare-earth abundances in indian kimberlite

Abundances of some rare-earth elements (REE), together with Hf, Ta, Th, and Ba have been determined by neutron activation analyses in twelve kimberlite samples from Peninsular India. The kimberlites have fractionated REE patterns with enrichment of light rare earths; La/Yb ratio varies from 39 to 166. A systematic relationship exists between the total rare-earth abundances and the petrochemistry of the rocks. The rare-earth abundances observed in the kimberlites are consistent with their derivation by partial melting of a hydrous garnet peridotite mantle and subsequent fractional crystallization of the melt.     

Adakitic rocks at convergent plate boundaries: Compositions and petrogenesis

Science China Earth Sciences - Adakitic rocks are intermediate-acid magmatic rocks characterized by enrichment in light rare-earth elements, depletion in heavy rare-earth elements, positive to...     

The Geochemistry of Volcanogenic Mineralization in the Northwestern Segment of the Pacific Ore Belt: Northeast Russia

This paper considers the geochemistry of volcanogenic mineralization in the northeastern segment of the Pacific Ore Belt (Northeast Russia). We give new evidence for the compositions and concentrations of trace and rare-earth elements (REE) in the ores of volcanogenic fields: Au-Ag epithermal (of various types and ages), Cu-Mo-Au porphyritic, Au-Bi related to granitoidal intrusions, Sn-Ag subvolcanic and kies polymetallic enriched in Au and Ag, as well as REEs in alkaline volcanic rocks. Geochemical signatures have been compiled for 17 formation types of volcanogenic fields. It was found that the ore-forming fluids in most fields belonged to an NaCl-H₂O hydrothermal system that was enriched in Cl relative to F; the values of Y/Ho in the ores of nearly all types correspond with the interval of ratios characteristic for present-day hydrothermal fluids in backarc basins; most of the ores that we studied had near-chondrite spectra with configurations similar to those of the REE spectra in volcanic rock sequences of the andesite-diorite series. Comparative analysis of REE spectra in the distribution of trace elements over classes of gold concentration shows synchronous enrichment of ores in similar sets of trace elements. The high Co/Ni ratio in volcanogenic ores probably reflects the superposition of a later magmatic fluid upon an earlier mineralization. Samples from ores of volcanogenic fields, except for Kuroko, show δCe and δEu varying from negative to mildly positive values, thus indicating low-oxidizing conditions during deposition. It was found for Au-Ag epithermal ores that they are enriched in a wide range of trace elements; they have low concentrations of REEs, the light REEs are more abundant than the heavy ones, and the Eu anomalies vary considerably from small negative to low and high positive values. The results provide evidence of an exhalation hydrothermal origin of the Khotoidokh field. It has been shown that the REEs in the ores of the Bol’shoe field are of the type that is most valuable to industry. The results can be used to deal with practical problems: determining the formation type and evaluating the industrial value of a field; detecting accessory components in ores; and discriminating between the types of geochemical anomalies (in rocks or in soil) and stray fluxes as to the potential of a field.     

Trace element mobility in the mylonite zone within the ophiolite aureole,St. Anthony Complex,Newfoundland

The late syntectonic mylonite zone (45–100 m thick) within the dynamothermal aureole of the St. Anthony Complex in northwestern Newfoundland was derived from surrounding quartz and epidote amphibolites by deformation and the nearly isovolumetric metasomatism. Amphibolites have a composition typical of light REE-depleted ocean-floor tholeiites. Mylonites (biotite amphibolites) resemble transitional alkali basalts in major and trace element composition and in the interrelation among relatively immobile elements such as Ti, Zr, Nb, Y and P. Their REE patterns are enriched in light REE and show gradual depletion of heavy REE with La/Yb ratios ranging from 8.4 to 18.4. The results emphasize the need for caution in interpreting the concentration and ratios of any elements in mafic rocks which have been affected by metasomatism in an amphibolite facies shear zone.     

Origin of the anomalies in light and middle REE in sediments of an estuary affected by phosphogypsum wastes (south-western Spain)

Sc, Y, Th, Cu and rare earth elements (REE) concentrations have been analyzed in 14 samples of surface sediments and in two gravity cores by means of ICP-MS. Mean concentrations of Sc, Y and Th in surface sediments are 6.23, 4.76 and 16.30 ppm, respectively, lower than those present in the Upper Continental Crust (UCC). Cu concentration in these sediments is very high, 1466 ppm, and is caused by inputs from the Odiel and Tinto rivers, affected by acid mine drainage. SigmaREE mean concentration is 106.8 ppm, lower than that observed in other rivers and estuaries. In the cores, Sc, Y and Th concentrations show a significant increase in the intermediate levels, between 10 and 40 cm depth. The same pattern exists with Cu, where concentrations of 4440 ppm can be reached. Vertical evolution patterns for Sc, Y, Cu and heavy REE (HREE) are similar, and contrary to those shown by Th, light REE (LREE) and middle REE (MREE). Plots of North American Shale Composite (NASC)-normalized REE data of surface sediments show a slight depletion in REE concentrations. Most samples present with middle REE enrichment relative to light REE and heavy REE. Conversely, samples of the intermediate levels of the cores show significant enrichment of REE relative to NASC and high values in the (La/Gd)NASC and (La/Yb)NASC ratios. These anomalies in the fractionation patterns caused by enrichments in LREE and MREE concentrations is related to the presence of high concentrations of Th. They were generated by effluents from fertilizer factories between 1968 and 1998 which used phosphorite as source material.     

Importance of vertical geochemical processes in controlling the oceanic profiles of dissolved rare earth elements in the northeastern Indian Ocean

Vertical profiles of dissolved rare earth elements (REEs) were obtained in the Bay of Bengal and the Andaman Sea. The REE concentrations at various depths in the Bay of Bengal are the highest in the Indian Ocean. This is attributable ultimately to the large outflow of the Ganges–Brahmaputra and Irrawaddy rivers, but the dissolved REE flux to surface waters alone cannot explain the large and near-constant REE enrichment throughout the entire water column. The underlying fan sediments serve as not a source but a sink for dissolved REE(III)s. Absence of excess ²²⁸Ra in the deep waters suggests that lateral input of dissolved REEs from slope sediments is also small in these regions. Partial (<0.3%) dissolution of detrital particles, which are carried by the rivers and lateral surface currents and subsequently settle through the water column, appears to be a predominant source for the dissolved REEs. Vertical profiles showing an almost linear increase with depth are common features for the light and middle REEs everywhere, but their concentration levels are variable from basin to basin and from element to element. This suggests that their oceanic distributions respond quickly to the variation of particle flux and its REE composition through reversible exchange equilibrium with suspended and sinking particles much like the case for Th. The relative importance of the vertical geochemical processes of reversible scavenging over the horizontal basin-scale ocean circulation with passive regeneration like nutrients decreases systematically from the light to the heavy REEs. Using a model, the mean oceanic residence times of REEs in the Bay of Bengal are estimated to range from 37 years for Ce to 140–1510 years for the strictly trivalent REEs. In the deep water of the Andaman Sea, isolated from the Bay of Bengal by the Andaman–Nicobar Ridge (maximum sill depth of ∼1800 m), the REE concentrations are almost uniform presumably due to rapid vertical mixing. The REE(III) concentrations are similar to that of ∼1250 m depth water in the Bay of Bengal, consistent with other oceanographic properties. However, the REE composition of the deep water appears to be altered slightly by preferential scavenging of the light REE(III) at the bottom boundary of the basin.     

Rare earth element and other trace element distribution,and the origin of the iblean magmas

In the Iblean region, southeast Sicily, a sequence of subaqueous and subaerial volcanics is interlayered in sedimentary levels, Upper Miocene to Lower Pleistocene in age. These rocks range from low-K tholeiites to basanites.Rare earth elements (REE) have been determined by instrumental neutron activation analysis in five samples, and other trace elements (Li, Rb, Sr, Co, Cr, Cu, Ni) by atomic absorption spectrophotometry in thirteen samples, already analyzed also for major elements.The tholeiites differ systematically from rocks of the alkalic suite for elements like Li, Sr and light REE (Sr < 200 ppm, Ce ? 15 ppm in the former; Sr > 500 up to 2000 ppm, Ce > 150 ppm in the latter), while Ni, Co, Cr and heavy REE ranges overlap in the two rock suites.The results agree in indicating different degrees of partial melting, probably at different levels in a heterogeneous mantle, as responsible for the origin of most of the rocks found in the Iblean region: the tholeiites should have been formed at relatively shallow depth by fusion of large proportions of a depleted mantle, while increasingly undersaturated volcanics of the alkalic suite have been probably generated at greater depth by partial melting of decreasing amounts of mantle material.     

Provenance for the Chang 6 and Chang 8 Member of the Yanchang Formation in the Xifeng area and in the periphery Ordos Basin: Evidence from petrologic geochemistry

Study indicates that the major paleocurrent and source direction for the Chang 8 Member of the Yangchang Formation, Upper Triassic in the Xifeng area of the southwestern Ordos Basin derived from the southwest direction with the southeast source as the subordinate one. While the Chang 6 Member was influenced not only by the same source as that of the Chang 8 Member from the southwest and the southeast direction, but also affected by the northeast and the east provenance around the Ordos Basin, based upon measurement of paleocurrents on outcrops located in the periphery Ordos Basin, analysis of framework grains and heavy minerals in sandstones of the Chang 6 and Chang 8 Members and their spatial distribution in the study area, combined with characteristics of trace elements and rare-earth elements of mudstones and of a small amount of sandstones in the Xifeng area and outcrops in margin of the Ordos Basin. The Yuole-Xuanma-Gucheng-Heshui-Ningxia region located in the northeastern and the eastern Xifeng area was the mixed source area where the southwest, southeast, northeast and the east sources were convergent till the Chang 6 Member was deposited. The rare earth elements of the Chang 6 and Chang 8 Members are characterized by slight light rare earth-elements (LREE) enrichment and are slightly depleted in heavy rare earth-elements (HREE) with weak to moderate negative abnormal Eu, resulting in a right inclined REE pattern, which implies that the source rocks are closely related with better differential crust material. Analysis on geochemical characteristics of the mudstones and sandstones, features of parent rocks in provenance terranes and tectonic settings shows that source rocks for the Chang 8 Member mainly came from metamorphic and sedimentary rocks in transitional continental and basement uplift terranes with a small amount of rocks including metamorphic, sedimentary and igneous rocks coming from mixed recycle orogenic belt located in the southwest margin of the Ordos basin. Rocks in the crystalline basement and the overlying sedimentary cover in a basement uplift setting in the northeast periphery of the basin also contributed a part of the sources for the Chang 6 Member, in addition to the sources deriving from transitional continental and basement uplift terranes in the southwest margin of the basin. Parent rocks of the provenance terrane in the northeast margin of the Ordos Basin are characterized by having more felsic rocks.     

Rare earth element mobility during granite alteration: Evidence from southwest England

Geochemical analyses of granitic rocks from southwest England reveal that the rare earth elements (REE) were potentially mobile during hydrothermal and supergene alteration. In particular, trivalent REE were removed from the system during K-silicate alteration, Eu was lost during sericitic alteration; all REE were lost during tourmalinization, and light REE were lost during chloritization and argillic alteration. The fluids themselves had low concentrations of REE; in only one case (chloritization) were heavy REE introduced during alteration. Analysis of separated minerals indicated that the behaviour of the REE could be partly explained in terms of their different affinities for the primary and secondary assemblages. Thermodynamic calculations indicated that REE mobility is enhanced by the presence of fluorine in the alteration fluids partly because REE form more stable complexes with F than with Cl and partly because elements such as Ti, Zr and P that form REE-bearing minor phases are themselves potentially mobile.     

Rare earth elements in the pore waters of reducing nearshore sediments

The REE are mobile during early diagenesis in reducing nearshore sediments of Buzzards Bay leading to greatly enhanced concentrations in pore waters, e.g. 815 pmol kg⁻¹ Nd and 1910 pmol kg⁻¹ Ce within 30 cm of the sediment-seawater interface, about 10–50 times local seawater values. Two principal diagenetic reactions have been identified. Preferential Ce enrichment (positive Ce anomalies) and preferential heavy REE enrichment (light REE removal) in the pore waters is associated with redox cycling of Fe and Mn within the upper few centimeters of the sediment. Release of REE, without fractionation, from sediments and addition to pore waters occurs deeper within the sediment column. The impact on the bulk sediment chemistry is undetectable but the porewater gradients imply that there are significant dissolved REE fluxes, both internal to the sediment system and across the sediment-seawater interface.     

Trace and rare earth element geochemistry of the black and grey shales of the Calabar Flank,Southeastern Nigeria: constraints on the depositional environment and the degree of metal enrichment

This study focuses on the trace and rare earth elements(REE) geochemistry of the Nkporo and Ekenkpon Shales of the Calabar Flank.The main aim is to infer their depositional environment and the degree of their metal enrichment.The shale samples were analyzed using inductively coupled plasma mass spectrometry.The results indicated that the mean concentrations of K,Na,and Fe in Nkporo and Ekenkpon Shales are 1.45,0.4,and 4.17 wt%,and 1.11,0.44,and 5.42 wt%;respectively.The Nkporo Shale is enriched with the following trace elements;PMn Sr Ba Zn Ce Rb Zr VCr Ni and depleted in the following trace elements;Ta GeSb Bi Cd Ag Te In Hg.While the Ekenkpon Shale is enriched with the following trace elements;P Mn Ba Sr VCe Zr Rb Cr Zn Ni and depleted in;Sb Ge Bi Ag Ce Te InHg.The concentration of redox-sensitive elements such as V,Ni,Mo,U,Cu,Cr,Re,Cd,Sb,Ti,Mn,and their ratio V/Mo and U/Mo in the black and grey shale samples show different patterns.The REE obtained from the Nkporo and Ekenkpon Shales were PAAS normalized.The Nkporo Shale showed a slightly flat light rare-earth element(LREE),middle rare-earth element(MREE),and heavy rare earth element(HREE) pattern enrichment.Ce/Ce*ranges from 0.95 to 1.09 in Nkporo Shale and 0.67 to 1.40 in Ekenkpon Shale.The Ekenkpon Shale showed a slight LREE,MREE enrichment,and depleted HREE patterns.The Mn contents and U/Mo ratio in Nkporo and Ekenkpon Shales suggests a poor oxygen transitional environment.The V/Mo and V/(V+Ni) ratios indicated that the Nkporo shales were deposited in an anoxic to suboxic conditions and Ekenkpon shales were also deposited under an anoxic to suboxic conditions.The V/Ni ratio indicated that the organic matter in the Nkporo shale is terrigenous while that of the Ekenkpon shales are both terrigenous and marine in origin.     

Trace element characteristics of the fluid liberated from amphibolite-facies slab: Inference from the metamorphic sole beneath the Oman ophiolite and implication for boninite genesis

Major and trace element compositions of amphibolites and quartzose rocks in the 230-m-thick metamorphic sole underlying the mantle section of the Oman ophiolite in Wadi Tayin area were determined to investigate the chemical characteristics of the hydrous fluid released from subducted amphiboltie-facies slab. The fluid-immobile element compositions indicate that protoliths of these rocks are mid-ocean ridge basalt-like tholeiite and deep-sea chert, which is consistent with the idea that these rocks represent Tethyan oceanic crust overridden during the early, intraoceanic thrusting stage of the Oman ophiolite emplacement. The rare-earth element (REE) and high field-strength element concentrations of the amphibolites show limited variations, within a factor of two except for a few evolved samples, throughout transect of the sole. On the other hand, concentrations of fluid-mobile elements, especially B, Rb, K and Ba, in amphibolites are highly elevated in upper 30 m of the sole (> 600 °C in peak metamorphic temperature), suggesting the equilibration with evolved, B-Rb-K-Ba-rich fluids during prograde metamorphism. The comparison with amphibolites in the lower 150 m (500 to 550 °C) demonstrates that the trace element spectra of the fluids equilibrated with the high-level amphibolites may vary as a function of metamorphic temperature. The fluids are characterized by striking enrichments of B, Rb, K and Ba and moderate to minor enrichments of Sr, Li, Be and Pb. At higher temperature (up to 700 °C), the fluids become considerably enriched in light REE and Nb in addition to the above elements. The estimated trace element spectra of the fluids do not coincide with the compositions of basalts from matured intra-oceanic arcs, but satisfactorily explain the characteristics of the low-Pb andesites and boninites found in the Oman ophiolite. Compositional similarity between the boninites of Oman and other localities suggests that the fluids estimated here well represent the amphibolite-derived fluids involved in the magmatism of immatured, hot, shallow subduction zones.     

The distribution of trace elements in surface continental waters and the character of their migration in water

The results of studying the elemental composition of surface continental waters in the European Russia from tundra to arid zone are discussed. The relative concentrations of elements in the solid residue of waters from various natural-climatic zones are evaluated, and the enrichment or dispersion of continental waters by these elements are analyzed as compared with their clarkes in the rocks that occur in the catchment areas. The coefficients of migration in water are evaluated, and the major elements with respect to which surface waters enrich under anthropogenic load are identified. The territorial distribution of higher concentrations of the most hazardous elements in waters of lakes is characterized.     

An evaluation of the behavior of the rare earth elements during the weathering of sea-floor basalt

We present rare earth element (REE) data for fresh and altered tholeiitic basalts sampled during a dredging transect at 23°N in the Atlantic Ocean and covering a time span of 0 to 57 million years. These data have been used to evaluate the behavior of the REE during low-temperature weathering processes. Compositional trends from altered basalt interiors to palagonitized rinds in individual pillow samples indicate significant mobility of the light REE: some elements are enriched by four orders of magnitude in rinds relative to interiors. The heavy REE show no selective mobilization and can be used in a normalization procedure which indicates that the light REE are enriched in altered interiors relative to fresh interiors of the basalts. Cerium behaves anomalously and accords with either its abundance in seawater or its fractionation from seawater during the formation of ferromanganese deposits.These results indicate that REE data from fresh glassy or crystalline basalt samples only may be used with confidence in petrological models.     

Behaviour of rare earth elements during hydrothermal alteration at the Buena Esperanza copper-silver deposit, northern Chile

A study of the REE behaviour in alteration zones of the Buena Esperanza subvolcanic CuAg deposit, located in the Coastal Range of northern Chile, reveals that the elements are mobile in the rocks during alteration. The ore-forming process developed in three different stages of alteration-mineralization.

The hydrothermal alteration of the early and middle stages affected basaltic fragments of a breccia pipe. La and Ce were leached from the rock fragments located at the bottom and at the middle part of the breccia pipe and partly redeposited at the top during alteration. Sm, Eu and Tb were released selectively and the heavy REE behaved as relatively immobile elements. Sericite is the most important alteration mineral for fixing the REE during this stage. The incoming fluids had low REE contents.

The late stage of hydrothermal alteration happened simultaneously with the intrusion of a gabbroic volcanic neck, affecting mainly these subvolcanic rocks. REE patterns of samples from the top and bottom of the alteration zone exhibit roughly parallel trends, but are systematically enriched in REE in comparison to unaltered samples. This enrichment seems to be more intensive at the top of the altered area coinciding with the enrichment of Rb, K and Cu in these rocks. Epidote plays the most important role for fixing this hydrothermal input of REE during the latest stage of alteration.     

The pliocene volcanism of the voras Mts (Central Macedonia,Greece)

Major element chemistry, K/Ar ages and trace element data are reported for volcanic rocks from the Voras volcanic complex of Central Macedonia (Greece). Petrological data show that the Voras volcanic rocks consist essentially of intermediate members of the high-K calc-alkaline and shoshonitic series, the most abundant rock types being high-K andesites and dacites, latites and trachytes. K/Ar ages determined on selected samples show values ranging between 5.0 and 1.8 m.y., indicating that the Voras volcanism was active from Pliocene up to the Lower Pleistocene. The high Th, Hf, Ba and LREE shown by some representative samples together with their strongly fractionated light and heavy REE patterns and the absence of significant negative Eu anomalies indicate a magma genesis by low degrees of partial melting of a source enriched in large ion lithophile elements, leaving a garnet-bearing and plagioclase-free residue. This source is believed to be represented by a mantle garnet peridotite enriched in incompatible elements. The geotectonic significance of the K-rich volcanism of the Voras area is discussed within the general framewoek of the late Tertiary tectonic evolution of the Aegean area and its emplacement is related to the distension tectonic movements which have affected the boundary area between the Macedonian microplate and the European craton since the Neogene.     

Petrogenetic relationships of acid and basic rocks in iceland: Sr-isotopes and rare-earth elements in late and postglacial volcanics

Strontium isotope ratios and rare-earth element abundances have been measured in acid, intermediate and basic rocks from three late to postglacial volcanic complexes, and several other postglacial basalts in Iceland. Late and postglacial basalts in Iceland have been generated from a source region which is essentially homogeneous with respect to⁸⁷Sr/⁸⁶Sr. The mean⁸⁷Sr/⁸⁶Sr ratio for the basalts analysed is 0.70328 and the range is from 0.70317 ± 6to0.70334 ± 5 (2σ).Acid rocks from the Kerlinganfjöll and Namafjall volcanic complexes have⁸⁷Sr/⁸⁶Sr ratios which are indistinguishable from analysed basalts from the same complexes. However, intermediate and acid rocks from the Torfajökull complex have significantly higher⁸⁷Sr/⁸⁶Sr ratios and could not have been derived by fractional crystallization from basaltic magmas similar to those found in the same complex. These latter rocks have most probably been produced by remelting of Tertiary gabbroic rocks in Layer 3. Most of the basalts analysed have higher total rare-earth element abundances than typical dredged ocean-ridge tholeiites, and show less light rare-earth depletion. Intermediate and acid compositions show overall higher abundances and light rare-earth enrichments. The measured rare-earth abundances are compared with abundances generated by differential partial melting of various model source regions.It is shown that both the tholeiitic and alkali basalt compositions could be generated from the same source material by different degrees of partial melting. Variable partial melting of gabbroic material may account for the rare-earth element abundances of both the rhyolitic rocks (small degrees of melting) and the intermediate rocks (more extensive melting).     

Geochemistry of upper cretaceous volcanic rocks from the pontic chain,northern turkey

Preliminary data on major elements, Cs, Ba, Rb, Pb, Sr, REE, Y, Th, U, Zr, Ht, Sn, Nb, W, Mo, Cr, V, Sc, Ni, Co and Cu contents for eight samples coming from the Upper Cretaceous volcanic belt of the Pontic Chain (Northern Turkey) are reported. SiO, versus K₂O relationship shows that the analyzed samples belong to the calc-alkaline and shoshonite series. The calc-alkaline rocks appear to represent two distinct magma types one close in composition to typical island are calc-alkaline magmas and one with high incompatible elements concentration and tractionated heavy REE patterns which suggest a genesis by partial melting at high pressure with a garnet bearing residue. Shoshonitic rocks show Na₂O/K₂O close to one, high incompatible elements concentration, and TiO₂%. Al₂O₃%, Ni and Co contents, Ni/Co and V/Ni ratios and REE patterns similar to typical island are andesites which suggest for these rocks similar genetical processes as the island are calc-alkaline magmas.     

Petrography and geochemistry of manganiferous rocks in the Mankwadzi area in the southern Kibi‐Winneba metavolcanic belt,Ghana: Implications for genesis of Mn formations in the Birimian of West Africa

Manganiferous rocks in the Mankwadzi area in the southernmost portion of the Kibi‐Winneba metavolcanic belt, one of several Mn occurrences in the Paleoproterozoic Birimian of Ghana, are hosted in hornblende schist and amphibolite. These rocks are, in places, intruded by hornblende dyke. In outcrop, the manganiferous rocks appear to be conformable with the host schist and amphibolite, are macroscopically dark, fine‐grained and structurally massive to distinctly banded. Observed alternating light and dark occasionally macro‐folded bands suggest post‐depositional deformation of both light and dark bands. Microscopic observations revealed that the light bands are dominantly Si‐rich and the dark bands mainly of opaque minerals. Whole rock analyses of the manganiferous rocks show high contents of MnO (16.75–27.4 wt%) suggesting that the opaque minerals are likely rich in Mn. The analyzed rock samples show moderate to strong enrichments in light rare earth elements compared to heavy rare earth elements. Whereas the manganiferous rocks show perceptibly negative Eu anomaly, host hornblende schist and hornblende dyke do not. Eu anomaly in amphibolite samples is, however, uncertain as the three samples analyzed gave positive, negative and no Eu anomalies. Based on the field characteristics, microscopic and geochemical features, we suggest that the Mn occurrence in the Mankwadzi area originated via sedimentary deposition and was later modified by metamorphism, hydrothermal and/or supergene processes similar to manganiferous occurrences at Nsuta and Tambao in the Birimian of West Africa.