Light Rare Earth Element Depletion Research Articles

Petrogenesis and tectonic setting of the proto-tethyan dachaidan ophiolite, North China: insights from clinopyroxene chemistry and whole-rock Sr–Nd–Pb and zircon Hf isotopes

IntroductionThe Dachaidan ophiolites outcrop within an ultrahigh-pressure metamorphic belt along the northern margin of the Qaidam Basin. However, their age, source, and tectonic setting remain still in debate.MethodIn this study, we investigated the geochemistry and geochronology of the Dachaidan ophiolitic gabbros.Results and DiscussionZircon U–Pb dating yielded a crystallization age of 510.0 ± 2.8 Ma and 510.0 ± 2.9 Ma for the gabbro. The gabbros have low SiO2 contents (47.15–50.10 wt.%) and high MgO contents (6.35–9.04 wt.%) and Mg# values (55–74). The total rare earth element (∑REE) contents are 8.35–28.07 ppm, lower than those of normal-type mid-ocean ridge basalts (MORBs), and the gabbros exhibit light REE depletion or flat REE patterns, with small positive Eu anomalies (Eu/Eu* = 1.06–1.40). Trace element patterns are depleted to enriched in Nb and Ta, similar to island arc rocks and MORB. Clinopyroxene thermobarometry indicates the parental magma of the gabbros formed by high-temperature (1,318°C–1,363°C) and medium-pressure (1.27–1.64 GPa) partial melting in a mantle wedge. The gabbros have depleted Sr–Nd–Pb-Hf isotopic compositions, with (87Sr/86Sr)i = 0.704586–0.707441, εNd(t) = 4.7–6.6, and zircon εHf(t) = 7.6–11.4. The age-corrected Pb isotope ratios of these volcanic rocks are variable, with 206Pb/204Pb(t) = 18.085–18.253, 207Pb/204Pb(t) = 15.595–15.614, and 208Pb/204Pb(t) = 37.880–38.148, which are similar to the isotopic compositions of typical Indian MORBs. The source of the Dachaidan ophiolite is inferred to have been depleted mantle. The Dachaidan ophiolite likely formed in a forearc oceanic setting along the northern margin of the Qaidam Basin, during the initial subduction of an oceanic plate.

Accumulation of rare earth elements in human gallstones: a perspective from dietary and human health

BackgroundGallstone disease poses a global threat to human health and is strongly linked to environmental factors. However, there is currently no data on the presence of rare earth elements (REEs) in human gallstones. This paper investigates the concentration and distribution of REEs in gallstones for the first time, aiming to explore the environmental implications on human health.MethodsA total of 25 gallstone samples were collected in Shanghai and the content of REEs was measured by Inductively coupled plasma-Mass Spectrometry (ICP-MS) to explore the distribution of REEs in gallstones.ResultsThe concentration of REEs in gallstones ranged from 4.89 to 190.8 ng/g (mean 39.21). In most of the gallstone analyses, REEs have been detected and generally attributed to environmental exposure or food contamination. The Y/Ho ratio of gallstones was lower than that of continental rocks, similar to that in the blood, indicating limited fractionation during fluid transport processes in the gallbladder.ConclusionsThe upper continental crust (UCC)-normalized REEs pattern in gallstones showed depletion of light REEs, while most showed enrichment of heavy REEs. Positive Gd anomalies were found in most samples, while few samples suggested anthropogenic influence. Whether exogenous inputs or in vivo biofractionation lead to changes in REEs fractionated patterns require further analyses.

Y-Ho fractionation during basalt alteration in hydrothermal system: An implication for superchondritic Y/Ho signature recorded in Precambrian banded iron formations

The concentration of rare earth elements (REE) in Precambrian sedimentary rocks is widely used to estimate their depositional environment. Specifically, superchondritic Y/Ho value is a powerful indicator for determining whether a sedimentary rock was deposited in a marine environment. Currently, superchondritic Y/Ho value in seawater is believed to result from the preferential adsorption of Y onto Fe-Mn oxides. In modern oceans, Fe-Mn oxides are considered the sink for subchondritic Y/Ho value. On the contrary, Precambrian banded iron formations (BIFs) display superchondritic Y/Ho value, suggesting that Precambrian seawater also possessed a superchondritic Y/Ho value. However, Precambrian BIFs cannot account for the sink of subchondritic Y/Ho value. Thus, other processes must have been responsible for maintaining the superchondritic Y/Ho value of Precambrian seawater. A hydrothermal experiment involving mid-ocean ridge basalt (MORB) and a Cl-rich fluid was conducted at 300 °C and 500 bars to assess the role of basalt-hosted hydrothermal systems on the Y/Ho value of seawater. Over time, the fluid's Ca concentration increased while Na decreased, suggesting plagioclase albitization occurred. The REE pattern of the reacted fluids exhibited superchondritic Y/Ho values up to 63.2. Based on the presence of positive Eu anomaly and the degree of light REE depletion, the REE in the hydrothermal fluids was mainly sourced from plagioclase during albitization. The superchondritic Y/Ho values in the fluids can be explained by the preferential leaching of these elements due to differences in chloride complexing strength between REE. Subchondritic Y/Ho values observed in Precambrian hydrothermally altered basalts may be interpreted as remnants generating superchondritic Y/Ho values in coexisting Precambrian hydrothermal fluids. Therefore, we believe that the superchondritic Y/Ho value of Precambrian seawater was maintained by basalt-hosted hydrothermal system.

1.38 Ga magmatism and the extension tectonics in East Kunlun, northern Tibetan Plateau

Numerous Paleo- to Mesoproterozoic magmatic rocks were emplaced during the assembly, accretion and break-up of the Columbia supercontinent, and are keys to illustrating the supercontinent circle. The geological, petrological, geochronological and geochemical data of the newly discovered meta-felsic and meta-mafic magmatic rocks from the Wulonggou area are presented in this study to shed light on the Mesoproterozoic geodynamic setting of the Central Kunlun Belt and the Qaidam Block. Zircon U-Pb geochronological results indicate that the crystallization ages of the meta-felsic samples are 1385–1376 Ma, and the meta-mafic is 1379 ± 25 Ma (MSWD=0.17). Samples from the meta-felsic unit have SiO2 contents of 68.37–73.03 wt% and belong to the high-K calc-alkaline series. They exhibit similar REE distribution patterns and display enrichment in light rare earth elements (LREES) and negative Eu anomalies. Enrichments in Rb, Ba, Th, U and K, depletion in Nb, Ta, Sr, P and Ti are seen in the primitive mantle-normalized trace element pattern diagram. Magmatic zircons from different meta-felsic samples yield variable εHf(t) values of −8.14 to + 9.37 corresponding to ca. 1.7–2.0 Ga two-stage Hf model ages. Samples from the meta-mafic unit have low SiO2 concentrations of 49.87–50.43 wt%, high contents of Fe2O3T, MgO, CaO and TiO2, and Mg# values of 52–58. They show low total REE concentrations of 19.8–30.4 µg/g, and depletion in LREES, flat HREES distribution patterns with (La/Yb)N of 0.27–0.53 and insignificant Eu anomalies. Flat distribution pattern of high field strength elements (HFSEs) is observed in the primitive mantle-normalized trace element pattern diagram. They display similar immobile elements’ concentrations and distribution patterns, low Ti/Y, Nb/Y, La/Yb, and high Nb/La ratios, comparable with the present-day normal middle ocean ridge basalt. Zircons from the meta-mafic sample have mostly positive εHf(t) values ranging from −0.10 to + 4.10 with a single stage Hf model ages of ca. 1.7–2.0 Ga. The geochemical result implies that the meta-felsic unit was generated by partial melting of the Paleoproterozoic juvenile mafic lower-crustal material with mantle attributions, and the meta-mafic unit was probably from partial melting of the lithospheric mantle. Synthesizing the above evidences, Wulonggou Mesoproterozoic meta-magmatic rocks are a bimodal suite formed in a continental extensional tectonic setting which is probably related to the break-up of the Columbia supercontinent.

In situ geochemistry of apatite: Petrogenetic and tectonic interpretations of Jurassic felsic magmatism in the Yanbian area, NE China

Geochemical analyses of individual minerals provide more detailed insights into the petrogenesis of igneous rocks than whole-rock analyses. This study conducted in situ geochemical and Nd isotope analyses of apatites from 10 Jurassic granitic plutons in the Yanbian area, NE China, to establish the petrogenesis and regional tectonic evolution. The results indicate that the apatite geochemistry of Jurassic granitoids in the Yanbian area was controlled primarily by the composition of parental melt. Post-magmatic alteration may lead to geochemical decoupling between apatite and parental melt, while Nd isotopes exhibit some resilience to such alterations. Apatites from Early Jurassic granitoids display characteristics that are consistent with an I-type origin, whereas those from Middle and Late Jurassic granitoids exhibit an adakitic affinity. Variations in apatite compositions indicate the fractional crystallization of other rare earth element (REE)-bearing minerals during magma evolution. The early crystallization of plagioclase and allanite led to decreases in Sr and Th contents in apatite, respectively, resulting in a negative Eu anomaly and light REE depletion. The fractional crystallization of titanite and hornblende resulted in the depletion of middle REE in apatite. Hornblende is regarded as the main residual phase in the magma source of Middle and Late Jurassic adakitic granitoids in the Yanbian area. Apatite Nd isotopic compositions suggest that the Jurassic granitoids in the Yanbian area originated from two crustal sources: the Central Asian Orogenic Belt and the North China Craton. Additionally, increasing trends in apatite Sr/Y and (La/Yb)N ratios from the Early to Late Jurassic suggest a gradual thickening of the regional crust, which is likely driven by the continentward migration of the subduction zone associated with the Paleo-Pacific Plate.

Quantifying the Criteria Used to Identify Zircons from Ore-Bearing and Barren Systems in Porphyry Copper Exploration

Abstract Zircon is a common mineral in igneous rocks, which is resistant to both chemical weathering and physical abrasion. Its chemistry can potentially be used to distinguish ore-forming porphyry magmas from barren magma systems. This study compiles >23,000 zircon analyses from >30 porphyry deposits, barren intrusions, and rivers to determine the principal geochemical characteristics of fertile zircons using predictive modeling, and compares them with traditional geochemical thresholds. The results show that the Eu/Eu* and Dy/Yb ratios, P content, and the curvature at the end of rare earth element (REE) patterns (λ3) are the most diagnostic characteristics of fertile zircons. The use of geochemical thresholds, as Boolean conditions, reach their maximum performance for Eu/Eu* and Dy/Yb (sensitivity [sens] = 0.73, specificity [spec] = 0.90), but it is outperformed by the random forest model (sens = 0.91, spec = 0.93) in the testing set. Explanatory analysis of the models shows that the fertility signal in zircons becomes stronger as the porphyry system evolves and is accompanied by an overall decrease in the middle to light REE and P content, characteristics that are absent in barren zircons. We attribute the observed difference in λ3 to the co-crystallization of other accessory phases, suggesting that the changes in the zircon Ce anomaly is controlled by the depletion of light and middle REE. The low P content in fertile zircons is caused by extensive crystallization of apatite. Fertile zircons have an excess of (REE + Y)3+, which we attribute to charge-balance by H+ in hydrous magmas. Simple machine learning algorithms outperform the traditional geochemical discriminators in their predictions and provide insights into characteristics that have not previously been considered for evaluating porphyry copper fertility using zircon geochemistry. We propose simplified methods that can be easily incorporated into exploration workflows.

Trace element variations in mussels' shells from continent to sea: The St. Lawrence system, Canada

Rare Earth Elements (REE) and several trace elements abundances in mussel's shells collected along the St. Lawrence River, the Estuary, and the Gulf of St. Lawrence (EGSL) reveal coherent chemical variations, with a sharp contrast between freshwater and seawater bivalves. In freshwater mussel's shells, Rare Earth Elements and Y (REY) patterns are rather flat. Their Mn and Ba concentrations are higher than those of EGSL mussel shells, which are much richer in Sr. Shale-normalized REY abundances in mussel's shells from the EGSL show positive anomalies in La and Y and well-marked negative anomalies in Ce, reflecting those of seawater. Prince Edward Island shells show light REE depletion relative to PAAS, positive La and Y anomalies, and negative Ce anomalies. Our data confirm the lack of detectable Gd pollution in the St. Lawrence River and in the EGSL, as well as Pb pollution at the mouth of the Saguenay Fjord and near Rimouski.

Nd isotope and element composition of shales from the Parnaíba Basin, NE Brazil: Insights for provenance shifts in a cratonic basin

Sm-Nd and Sr isotope compositions of 24 samples of fine-grained clastic rocks from eastern Parnaíba basin, NE-Brazil, are presented along with major and trace element compositions of 19 of these samples. Samples were collected from outcrops of the Paleozoic Canindé (Pimenteiras, Longá and Poti) and Balsas (Piaui Formation) groups, and from the Jurassic Pastos Bons Formation. Discrimination diagrams based on Th, Sc, La and Zr indicate sedimentary provenance from felsic dominant sources and high degrees of crustal recycling. PAAS-normalized REE diagrams show that the Pimenteiras and Longá Formations display flat patterns with slight REE enrichment, and initial εNd and 87Sr/86Sr around the average composition of the upper continental crust, respectively between −8.9 and −14.6 and between 0.711 and 0.760, indicating provenance from old Precambrian basement. The Nd TDM model ages of the Pimenteiras between 1.32 Ga and 2.00 Ga indicate heterogeneity of source areas during the Devonian, and TDM ages around 1.6 Ga in the Longá Formation samples suggest intense recycling of older sediments. The Poti formation samples yield TDM ages of 2.30 Ga and 2.32 Ga, respectively, suggesting tectonic reactivation and new input from Archean-Paleoproterozoic basement complexes. The Pastos Bons Formation samples show lower Th-Sc ratios, light-REE depletion, and less negative initial εNd, indicating contribution from mafic rocks, probably from the underlying Mosquito Formation intraplate tholeiitic basalts and dolerites.

Melting processes, cooling rates, and tectonic settings of the Neo-Tethyan mantle: the in-situ mineral chemical record

Peridotites in the Yarlung Zangbo ophiolite (YZO) have the potential to elaborate the mantle dynamics that operated below the Neo-Tethyan oceanic crust. Here, we measured major and trace element concentrations of minerals (e.g., clinopyroxene, orthopyroxene, olivine, and spinel) in YZO harzburgites and lherzolites to trace the origin and evolution of the YZO. The rare earth element (REE) patterns of clinopyroxenes in lherzolites and harzburgites plot within the field of abyssal and forearc peridotites, respectively, indicating that the latter experienced a higher degree of partial melting. Based on the relative extents of light (LREE) and heavy (HREE) REE depletions in clinopyroxene, we classified the lherzolites into two groups (I and II). The group I clinopyroxenes are depleted in HREEs and enriched in LREEs and MREEs compared to those of group II. Meanwhile, the REE patterns of harzburgite clinopyroxenes are identical to that of group II, although they display lower REE concentrations. Models based on REE abundances in clinopyroxene suggest that group I lherzolites experienced ~8–11% partial melting in the spinel domain, whereas group II lherzolites formed after 5% melting in the garnet domain followed by 6–9% and 9–16% partial melting in the spinel domain, respectively. These high degrees of melting may suggest that the harzburgites formed in a supra-subduction zone (SSZ) setting. Surprisingly, the REE-in-two-pyroxenes thermometer (TREE) shows that the YZO peridotites record high-temperature cooling at 991–1218 °C which is lower than the conditions below mid-oceanic ridges (MORs), but compatible with recent reports of high closure temperatures in forearc environments. Furthermore, our TREE results constrain the cooling rate of the YZO peridotites to ~0.01–0.5 °C/yr, overlapping with rates reported for SSZ, MOR, and abyssal peridotites. By integrating the petrological, geochemical, and thermal features, we tentatively interpret the group I lherzolites accreted in an Early Cretaceous forearc during subduction initiation, whereas the group II lherzolites and the harzburgites formed by further melting of the earlier lherzolites in a SSZ setting.

Fractional crystallization of garnet in alkali basalts at >1.8 GPa and implications for geochemical diversity of Large Igneous Provinces

A suite of lavas from northwest Mull, British Palaeocene Igneous Province, exhibit major and trace element characteristics that are best explained by very high pressure (>1.8 GPa) crystallization of an assemblage comprising aluminous clinopyroxene (Al-Cpx) plus garnet. The resulting series of consanguineous magmas are mildly Si-undersaturated. The trace element effects of this crystallizing assemblage are manifested in increasing light rare earth element (LREE) enrichment and heavy REE (HREE) depletion with decreasing whole-rock MgO, a predictable consequence of the bulk distribution coefficient (D) of this assemblage being > > 1 for HREE but <<1 for the LREE. Early crystallization of Al-Cpx and replacement of plagioclase feldspar by garnet in the crystallizing assemblage also results in increasing or near constant Al2O3 abundances in cotectic compositions with MgO < ∼7 wt%. Garnet as opposed to plagioclase crystallization is also reflected in the incompatibility of Sr and compatibility of Y resulting in very high Sr/Y lavas (up to 100) with high Sr (∼1200 ppm) and low Y contents (∼12 ppm). Lavas also have high Zr/Y (up to 30). Major element constraints suggest the crystallizing assemblage comprised ∼40% garnet and 60% Al-Cpx.Magmas that fractionated at ∼1.8 GPa rose to the surface without interacting with the continental crust. Immediately underlying basalts and picrites show evidence of crustal contamination and assimilated fusible portions of the crust, therefore effectively lining the plumbing system and allowing later magmas to rise to the surface without crustal contamination. A local change in tectonic regime from extension to passive appears to be linked to a change from low pressure to very high-pressure crystallization of magmas. Whilst evidence for garnet fractionation in continental flood basalts is very rare, this paper provides a characterization of its geochemical consenquences.

Origin of Erzgebirge ultrahigh‐pressure garnetite: Formation from a basaltic protolith by serpentinization‐assisted metasomatism?

AbstractErzgebirge ultrahigh‐pressure (UHP) garnet peridotite includes scarce layers of garnet pyroxenite, nodules of garnetite and, very rarely, of eclogite. Peridotite‐hosted eclogite shows the same subalkali‐basaltic bulk rock composition, mineral assemblage and peak conditions as gneiss‐hosted eclogite present in the same UHP unit. Garnetite has considerably more Mg, moderately enhanced Ca and Fe and significantly lower contents of Na, Ti, P, K and Si than eclogite, whereas Al is very similar. In addition, the compatible trace elements (Ni, Co, Cr, V) are elevated and most incompatible elements (Zr, Hf, Y, Sr, Rb and rare Earth elements [REE]) are depleted in garnetite relative to eclogite. In contrast to other large ion lithophile elements (LILEs), Pb (+121%) and Ba (+83%) are strongly enriched. The REE patterns of garnetite are characterized by depletion of light and heavy REE and a medium REE hump indicative of metasomatism, features being absent in eclogite. An exceptional garnetite sample shows an REE distribution similar to that of eclogite. Garnetite is interpreted to have formed from the same, but metasomatically altered, igneous protolith as eclogite. Except for Ba and Pb, the chemical signature of garnetite is explained best by metasomatic changes of its basaltic protolith caused by serpentinization of the host peridotite. Garnetite is chemically similar to basaltic rodingite/metarodingite. Although rodingite is commonly more enriched in Ca, there are also examples with moderately enhanced Ca matching the composition of Erzgebirge garnetite. Limited Ca metasomatism is attributed to the preservation of Ca in peridotite during hydrous alteration. This can be explained by incomplete serpentinization favouring metastable survival of the original clinopyroxene. In this case, most Ca is retained in peridotite and not available for infiltration and metasomatism of the garnetite protolith. This inescapable consequence is supported by the fact that clinopyroxene is part of the garnet peridotite UHP assemblage, which would not be the case if Ca had been removed from the protolith prior to high‐pressure metamorphism. The enrichment of compatible elements in garnetite is attributed to decomposition of peridotitic olivine (Ni, Co) and spinel (Cr, V) during serpentinization. Enrichment of Ba and Pb contrasts the behaviour of other LILEs and is ascribed to dehydration of the serpentinized peridotite (deserpentinization). This requires two separate stages of metasomatism: (1) intense chemical alteration of the basaltic garnetite precursor, together with serpentinization of peridotite at the ocean floor or during incipient subduction; and (2) prograde metamorphism and dehydration of serpentinite during continued subduction, thereby releasing Pb–Ba‐rich fluids that reacted with associated metabasalt. Finally, subduction to &gt;100 km and UHP metamorphism of all lithologies led to formation of garnetite, eclogite and garnet pyroxenite hosted by co‐facial garnet peridotite as observed in the Erzgebirge.

Genesis and depositional environment of the Carboniferous Baishanquan iron deposit in Eastern Tianshan, Northwestern China

Submarine volcanic-hosted iron deposits are the most important iron deposit in Northwestern China. However, their origin remains controversial. Here, we present detailed studies of the petrology, geochronology, geochemistry and FeSi isotopes of iron ores from Baishanquan deposit in Eastern Tianshan, Northwestern China. Similar to Precambrian banded iron formations (BIFs), the Baishanquan deposit is hosted in a volcanic-sedimentary succession, the iron ores are characterized by banding with alternate iron-rich and silica-rich layers, and the mineral assemblage is dominant by magnetite, quartz and Fe-silicates. The iron ores show distinct light rare earth elements (REE) depletion [(La/Yb)PAAS = 0.24–0.47], no significant Eu anomalies (Eu/Eu⁎ = 0.88–1.16), relatively high Y/Ho ratios (30–34), and δ30Si values in quartz from the iron ores ranging from −0.80 to 1.67‰. These data indicate mixed seawater and low-temperature submarine hydrothermal source for both the iron and silica. The absence of negative Ce anomalies suggests that the depositional environment was characterized by low oxygen conditions similar to modern oxygen minimum zones. Positive δ56Fe values in most magnetite (−0.45 to +1.02‰) suggest partial Fe(II) oxidation of the iron ores. Interestingly, the iron ores also contain relatively high Al2O3, CaO, MgO, and Zr concentrations, indicating that the sedimentary basin was subject to periodic clastic input. Indeed, zircon LA-ICP-MS UPb dating of interlayered dacite indicates that the Baishanquan volcanic-sedimentary rocks and associated iron ores were deposited at 327.3 ± 2.8 Ma (N = 25, MSWD = 0.52). This is significant because the appearance of these iron deposit provides direct evidence that marine ferruginous conditions – at least locally - may have still been present at Carboniferous period.

Geochemical Characteristics of Garnet from Zinc–Copper Ore Bodies in the Changpo–Tongkeng Deposit and Its Geological Significance

The Changpo–Tongkeng tin polymetallic deposit in Dachang, Guangxi, is a world-class, superlarge, polymetallic tin deposit consisting of lower skarn zinc–copper ore bodies and upper tin polymetallic ore bodies. Garnet is the main gangue mineral in the skarn zinc–copper ore bodies and has a granular texture. Based on hand specimens and microscopic observations, the existing garnet can be divided into two generations: an early generation (Grt I) and a late generation (Grt II). The results of electron probe microanalysis (EPMA) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) in situ microanalysis show that the contents of SiO2 and CaO in the garnets from the two generations present limited variations, while the FeOT and Al2O3 contents vary significantly, indicating the grossular–andradite solid solution series (Gro29–82And12–69). Compared with Grt I (Gro72And25), Grt II (Gro39And59) is Fe-enriched and oscillatory zoning is developed. The total rare earth element (REE) contents in the two generations of garnet are relatively low, showing light rare earth element (LREE) depletion and heavy rare earth element (HREE) enrichment patterns. Grt II has higher REE content than Grt I and exhibits significant negative Eu anomalies (δEu = 0.18–0.44). The contents and variation characteristics of the major and trace elements in the two generations of garnet suggest that there were variable redox conditions and water/rock ratios in the hydrothermal system during the crystallization process of garnet. In the early stage, skarnization was in a relatively closed and low-oxygen fugacity system, with hydrothermal diffusion metasomatism being dominant, forming homogeneous Grt I lacking well-developed zoning. In the late stage of skarnization, the oxygen fugacity of the ore-forming fluids increased, with infiltration metasomatism being dominant, forming Grt II with well-developed oscillatory zoning. The contents of Sn, As, W, In, and Ge in the garnets are relatively high and increase with the proportion of andradite. Sn in zinc–copper ore bodies mainly exists in the form of isomorphic substitution in garnet, which may be the main reason for the lack of tin ore bodies during the skarn stage. This paper compares the trace element contents in garnets from domestic skarn deposits. The results indicate that the Sn content and δEu in garnet can be used to evaluate the tin-forming potential of skarn deposits.

Whole Rock, Mineral Chemistry during Skarn Mineralization-Case Study from Tongshan Cu-Mo Skarn Profile

Studying the activation, migration and precipitation processes of ore-forming elements is essential for understanding the genesis and mechanisms of skarn deposits. A typical skarn profile formed by the intrusion of Yanshanian granodiorite into the Carboniferous carbonate strata was studied. The profile is highly consistent with the classic skarn profile, ranging from the intrusion, weak alteration belt, skarn belt (inner and outer skarn belt) and mineralization belt (mainly characterized by Cu mineralization) to the surrounding marble without being affected by late-stage low-temperature or supergene weathering alteration. Whole-rock data show that the major and trace elements exhibit relatively small changes in the granodiorite and inner skarn, but huge variation in the boundary between the inner and outer skarn; Na, Al, Ti and Sr show significant decreases, while Fe, Mg, Zn, V and Ni show significant increases. The elemental content in the outer skarn is 10–100 times or more higher than that in the marble, but the elements such as Ca, Sr and Cs diluted from the marble. During the migration process from the inner skarn to the outer skarn, some elements (such as K, Rb and Ba) were depleted in the inner, but not enriched in the outer, indicating that they may migrate to farther locations. Grossularite developed in the inner skarn, with light rare earth element (LREE) depletion and heavy REE enrichment, as well as positive and negative anomalies of Eu (δEu = 0.42–3.95). Andradite developed in the outer skarn, with zonation development, light REE enrichment, and heavy REE depletion and a positive Eu anomaly (δEu = 0.36–46.83). Some negative Eu anomalies appear at the edges of garnets in the outer skarn, indicating fluctuations in fO2 during the late skarn process. A positive correlation between Fe3+ and REE3+ in the garnets from the inner skarn, as well as between Al3+ and REE3+ from the outer skarn indicated that there are different YAG substitution mechanisms of REE between the inner and outer skarn. Low garnet REE contents and highly variable Y/Ho ratios in outer skarn suggest that the significant fluctuations in REEs may be primarily controlled by water-rock interactions. Considering the whole-rock major and trace element contents, as well as the trace element features of garnet, we found that whole-rock Na, Al, Ti and Sr elements, garnet Ti, Zr and Nb elements exhibit significant differences between the inner and outer skarn. These characteristics can be used to distinguish the boundary between the rock body and carbonate during the skarnification process.

Heterogeneous Subcontinental Lithospheric Mantle below the South Margin of the Siberian Craton: Evidence from Composition of Paleoproterozoic Mafic Associations

Abstract —Paleoproterozoic mafic associations of the Irkut block from the Sharyzhalgai uplift are gabbro-dolerite dikes and small gabbronorite and monzodiorite massifs, which formed at 1.87–1.84 Ga and were coeval with granitoids and basite intrusions of the South Siberian magmatic belt (SSB). All the Paleoproterozoic mafic associations of the Irkut block are characterized by the presence of biotite and alkali feldspar, enrichment in K2O, LILE, Th, and light REE, highly fractionated multielement spectra with sharp Nb and Ti depletion, and extremely low εNd(T) from –5.1 to –10.1. In these compositional features, they are similar to mafic complexes in the central and eastern parts of the SSB (the Baikal uplift and the western Aldan shield). Their geochemical and isotopic characteristics did not result from crustal contamination but point to derivation from the subcontinental lithospheric mantle (SCLM) enriched by reaction with felsic subduction-related and OIB-like mafic melts formed at a low degree of melting. The geochemically contrasting Paleoproterozoic gabbronorites in the Onot block of the Sharyzhalgai uplift are marked by depletion in K2O, Ba, LILE, Th, and light REE, weak depletion in Nb, and higher εNd(T) from –0.3 to –1.4. The gabbronorites indicate not only an increase in the contribution of a depleted source to their genesis but also the heterogeneity of the subcontinental lithospheric mantle below the south margin of the Siberian Craton. The formation of enriched SCLM domains throughout the South Siberian belt was mainly the result of Archean subduction-related metasomatic processes. The wide distribution of Paleoproterozoic mafic complexes with subduction geochemical signatures and negative εNd(T) on most early Precambrian cratons is due to global change in the composition and an increase in the heterogeneity of the subcontinental lithospheric mantle toward the end of the Archean.

Petrogenesis and tectonic setting of Early Cretaceous mafic dykes in the North Qinling Orogenic Belt, central China: constraints on the lithospheric lower crust delamination

Late Mesozoic mafic dykes, which are widely developed in the North Qinling Orogenic Belt (NQOB), include abundant geodynamic information. This paper describes the mafic dykes that intrude the Late Jurassic granite in the Dayu and Kuyu areas, and reports important petrological constraints for the late Mesozoic tectonic transition from compression to extension in the NQOB. Three zircon U–Pb results show that the minimum ages of the mafic dykes are 139.8 ± 1.4 Ma, 137.4 ± 1.7 Ma and 133.4 ± 0.9 Ma, indicating that the emplacement age of the Dayu and Kuyu mafic dykes is 140–133 Ma. Petrogeochemical analyses suggest that the mafic dykes belong to the high-K calc-alkaline shoshonite series with low SiO2 (46.93–56.73 wt%), MgO (1.88–9.10 wt%) and TiO2 (1.17–1.82 wt%), and high Al2O3 (13.98–17.46 wt%), TFe2O3 (7.81–10.92 wt%) and K2O (1.28–4.78 wt%). The mafic dykes are enriched in large ion lithophile elements (e.g. Rb, Ba, K, La, Sr) and depleted in high-field-strength elements (e.g. Nb, Ta, Zr, Ti). These samples have the right-sloping chondrite-normalised rare earth element patterns, which suggest light rare earth element enrichment and heavy rare earth elements depletion with no obvious Eu anomalies (δEu = 0.94–1.11). The I Sr, ε Nd(t), ε Hf (t) and T DM2(crust) values are 0.7056–0.7060, −10.60 to −5.98, −14.1 to −2.8, and 1382.4 ± 25.1 to 2081.9 ± 47.6 Ma, respectively. Both elemental and isotopic geochemistry show that the formation of Dayu and Kuyu mafic dykes is due to the partial decompression melting of previously enriched lithospheric mantle during a delamination process. The mafic dykes have undergone fractionation crystallisation of Mg–Fe phase minerals during magma ascent, accompanied by some crustal contamination. Combined with the regional tectonic setting, we suggested that the NQOB experienced intra-continental extension during the Early Cretaceous. KEY POINTS Early Cretaceous (140–133 Ma) mafic dykes have been discovered in the middle part of the North Qinling Orogenic Belt. The remote effect of the Paleo-Pacific Plate subduction has reached the middle of the North Qinling Orogenic Belt. The North Qinling Orogenic Belt entered the extensional stage in the Early Cretaceous (140–133 Ma).

Rare earth element signatures of Doushantuo cap dolostones capture an increase in oxygen in the anoxic Ediacaran ocean

The Rare Earth Element (REE) systematics of the post-Marinoan cap dolostones reflect the marine redox conditions and chemistry in the immediate aftermath of the snowball Earth. Rare earth elements and yttrium (REY) compositions in the Doushantuo cap dolostones that directly overlie Nantuo glacial diamictites in south China are determined from the inner shelf to the slope. In general, shale-normalized REY patterns (REYSN) of the cap dolostones show significant fractionations that are characterized by light REE depletion, slight middle REE enrichment relative to the light and heavy REEs, positive Eu anomalies, and slightly super-chondritic Y/Ho ratios. These dolostones, however, show no significant shale-normalized negative Ce anomalies. Such REYSN patterns are consistent with an extensive anoxic Ediacaran ocean in the shallow-to-deep water columns. The REE concentrations and normalized patterns in the cap dolostones vary spatially and stratigraphically. When compared to the shelf edge and the slope, cap dolostones from the inner shelf are distinguished by uniformly less fractionated REYSN patterns with an absence of Eu anomalies, and suppressed light REE depletion and MREE enrichment. These marked differences in the REYSN patterns indicate significant continental influences on the seawater chemistry within the restricted inner shelf (lagoon) during glacial meltdown. The temporal trends in the REY dataset of the Doushantuo cap dolostone reflect shifts in marine redox conditions. Dolostones from two thick shelf margin sections (5 m and 7 m thick, respectively) show almost identical stratigraphic trends in the REY concentrations, and the Ce, Y, and middle REE anomalies. The overall stratigraphic decrease in the Ce anomaly, accompanied by the increase in the Y anomaly and decrease in the middle REE anomaly towards the top of the rock unit, suggests that dissolved oxygen was increasing in the shallow water column during the deposition of the cap dolostones. The REE data in this study reveal that the oxygenation of the Ediacaran oceans started in the immediate aftermath of the snowball Earth (635–632 Ma).

Rare Earth Element Deposits in Mongolia

In Mongolia, rare earth element (REE) mineralization of economic significance is related either to the Mesozoic carbonatites or to the Paleozoic peralkaline granitoid rocks. Carbonatites occur as part of alkaline silicate-carbonatite complexes, which are composed mainly of nepheline syenites and equivalent volcanic rocks. The complexes were emplaced in the Gobi-Tien Shan rift zone in southern Mongolia where carbonatites usually form dikes, plugs or intruded into brecciated rocks. In mineralized carbonatites, REE occur mainly as fluorocarbonates (bastnäsite, synchysite, parisite) and apatite. Apatite is also present in the carbonatite-hosted apatite-magnetite (mostly altered to hematite) bodies. Alkaline silicate rocks and carbonatites show common geochemical features such as enrichment of light REE but relative depletion of Ti, Zr, Nb, Ta and Hf and similar Sr and Nd isotopic characteristics suggesting the involvement of the heterogeneous lithospheric mantle in the formation of both carbonatites and associated silicate rocks. Hydrothermal fluids of magmatic origin played an important role in the genesis of the carbonatite-hosted REE deposits. The REE mineralization associated with peralkaline felsic rocks (peralkaline granites, syenites and pegmatites) mainly occurs in Mongolian Altai in northwestern Mongolia. The mineralization is largely hosted in accessory minerals (mainly elpidite, monazite, xenotime, fluorocarbonates), which can reach percentage levels in mineralized zones. These rocks are the results of protracted fractional crystallization of the magma that led to an enrichment of REE, especially in the late stages of magma evolution. The primary magmatic mineralization was overprinted (remobilized and enriched) by late magmatic to hydrothermal fluids. The mineralization associated with peralkaline granitic rocks also contains significant concentrations of Zr, Nb, Th and U. There are promising occurrences of both types of rare earth mineralization in Mongolia and at present, three of them have already established significant economic potential. They are mineralization related to Mesozoic Mushgai Khudag and Khotgor carbonatites in southern Mongolia and to the Devonian Khalzan Buregtei peralkaline granites in northwestern Mongolia.

Geochemistry, zircon U-Pb chronology and Hf isotope composition of the Heishan’gou iron deposit in the Bikou Terrane, central China: Implication for the genesis of the Yudongzi banded iron formations

The Yudongzi banded iron formations (BIFs) are widely spread in the Neoarchean Yudongzi Group of the Bikou Terrane, Central China. Their sedimentary and metamorphic ages, however, remain controversial, either their forming or reworking processes. In this contribution, we conducted an integrated study of zircon U-Pb-Hf isotope geochemistry, as well as mineral and bulk-rock geochemistry on the Heishan’gou iron deposit, the largest iron deposit of the Yudongzi BIFs, to constrain their formation and metamorphism ages, source of ore-forming material and tectonic setting. Mineral chemistry analysis indicates that the amphibolite, host-rock of the Heishan’gou deposit suffered amphibolite facies metamorphism. LA-ICP-MS U-Pb dating of zircon grains from orthometamorphic host-rocks suggests that the Heishan’gou deposit was formed at the early Neoarchean (2781 ± 43 Ma for amphibolite and 2776 ± 43 Ma for plagioclase-hornblende schist), and metamorphosed at ca. 2480 ± 26 Ma and 1818 ± 44 Ma, respectively. The low contents of aluminum, titanium and high field strength elements in BIFs suggest that they are detritus-free marine chemical precipitates. The rare earth elements (REE) and Y patterns of BIFs display seawater-like signatures with light REE depletion, and positive La and Y anomalies. Meanwhile, their positive Eu anomalies suggest that submarine hydrothermal fluid might also be involved in the precipitation of BIFs. Combined with zircon Hf isotope data and geochemical compositions of amphibolites, it is proposed that the Yudongzi BIFs should be formed at back-arc basin setting. Compared with the representative Archean continent nucleus of the Yangtze Block (Kongling Complex), the Yudongzi Complex experienced distinct crustal evolutionary history. It indicates that the Yudongzi Complex might represent the accretionary block combined to the Yangtze continental nucleus later than the Paleoproterozoic.

A tool to distinguish magmatic from secondarily recrystallized carbonatites—Calcite/apatite rare earth element partitioning

Abstract Crustal geochemical signatures in carbonatites may arise from carbon recycling through the mantle or from fluid-mediated interaction with the continental crust. To distinguish igneous from fluid-mediated processes, we experimentally determined rare earth element (REE) partitioning between calcite/melt and apatite/melt at subvolcanic emplacement conditions (1–2 kbar, 750–1000 °C). Our data allow modeling of calcite-apatite (Cc/Ap) partition coefficients (D), representing a new tool to bypass the previously required but largely unknown carbonatite melt composition. Experimentally determined magmatic calcite/apatite REE patterns are flat, as is ~0.75, and they show a slight U-shape that becomes more pronounced with temperature decreasing from 1000 to 750 °C. Application to texturally well-equilibrated natural Ca-carbonatites and calcite-bearing nephelinites shows that some calcite-apatite pairs follow this pattern and, hence, confirm the magmatic nature of the carbonates. values of other mineral pairs range from 10−2 to 10−3, which, together with a substantial light REE depletion in the calcite, is interpreted as fluid-mediated light REE removal during secondary calcite recrystallization. Calcite/apatite REE distributions are well suited to evaluate whether a carbonatite mineralogy is primary and magmatic or has been affected by secondary recrystallization. In this sense, our tool provides information about the sample's primary or secondary nature, which is essential when assigning isotopic crustal signatures (in Ca, C, or Sr) or REE patterns to related geologic processes.