Metamorphic disturbances of magnetite chemistry and the Sm-Nd isotopic system of reworked Archean iron formations from NE Brazil

Iron formations are valuable archives of sedimentary conditions and post-depositional events.However,geochemical proxies commonly used to determine genetic characteristics can be variably modified during metamorphism and deformation,hampering their use as records of regional geological events.This work focuses on strongly reworked magnetite-quartz-rich rocks from the São Josédo Campestre Massif,one of the oldest fragments of preserved crust in South America.The genetic classification of these magnetite-quartz-rich rocks is not straightforward because primary assemblages and textures were variably modified by granulite facies metamorphism during a regional Paleoproterozoic migmatization event.To address genetic ambiguities,we analyzed their magnetite and pyroxene chemistry,wholerock geochemistry,and Sm-Nd isotopes.Magnetite chemistry indicates that pyroxene-poor iron formations(Type B)are low in trace elements such as Ti,Al,V,and Mn,suggesting a chemical similarity to iron formations elsewhere.In contrast,magnetites from pyroxene-enriched Type A iron formations are rich in trace elements and more akin to magnetite crystallized from higher temperature systems,such as skarn and IOCG.The^(147)Sm/^(144)Nd of these rocks show substantial variation even at the outcrop scale,indicating a locally-controlled,highly heterogeneous mixture of Archean,Paleoproterozoic,and Neoproterozoic sources.Therefore,our geochemical tools point out to heterogenous signatures of these magnetitequartz rocks and proxies compatible with both low and high-temperature conditions and age of deposition spanning sources from the Archean to the Neoproterozoic.We interpret that the studied São Josédo Campestre magnetite-quartz rocks represent Archean iron formations with original magnetite chemistry and isotopic signatures variably modified by metamorphism and by at least one deformation-related hydrothermal event.These results contrast with similar examples from China and Greenland where iron formations either preserved the magnetite chemistry or the primary isotopic signatures.Our study indicates that metamorphism can selectively affect chemical proxies used to study iron formations and undermine the genetic classification of iron ores.Thus,these proxies should be carefully applied in the interpretation of syn-depositional environments of polydeformed belts.

Genesis of the Nuri Cu-W-Mo Deposit,Tibet,China:Constraints from in situ Trace Elements and Sr Isotopic Analysis of Scheelite

The Nuri deposit is the only Cu-W-Mo polymetallic deposit with large-scale WO3 resources in the eastern section of the Gangdese metallogenic belt,Tibet,China.However,the genetic type of this deposit has been controversial since its discovery.Based on a study of the geological characteristics of the deposit,this study presents mineralization stages,focusing on the oxide stage and the quartz-sulfide stage where scheelite is mainly formed,referred to as Sch-A and Sch-B,respectively.Through LA-ICP-MS trace element and Sr isotope analyses,the origin,evolutionary process of the oreforming fluid and genesis of the ore deposit are investigated.Scanning Electron Microscope-Cathodoluminescence(SEMCL)observations reveal that Sch-A consists of three generations,with dark gray homogenous Sch-A1 being replaced by relatively lighter and homogeneous Sch-A2 and Sch-A3,with Sch-A2 displaying a gray CL image color with vague and uneven growth bands and Sch-A3 has a light gray CL image color with hardly any growth band.In contrast,Sch-B exhibits a‘core-rim’structure,with the core part(Sch-B1)being dark gray and displaying a uniform growth band,while the rim part(Sch-B2)is light gray and homogeneous.The normalized distribution pattern of rare earth elements in scheelite and Sr isotope data suggest that the early ore-forming fluid in the Nuri deposit originated from granodiorite porphyry and,later on,some country rock material was mixed in,due to strong water-rock interaction.Combining the O-H isotope data further indicates that the ore-forming fluid in the Nuri deposit originated from magmatic-hydrothermal sources,with contributions from metamorphic water caused by water-rock interaction during the mineralization process,as well as later meteoric water.The intense water-rock interaction likely played a crucial role in the precipitation of scheelite,leading to varying Eu anomalies in different generations of scheelite from the oxide stage to the quartz-sulfide stage,while also causing a gradual decrease in oxygen fugacity(fO2)and a slow rise in pH value.Additionally,the high Mo and low Sr contents in the scheelite are consistent with typical characteristics of magmatic-hydrothermal scheelite.Therefore,considering the geological features of the deposit,the geochemical characteristics of scheelite and the O-H isotope data published previously,it can be concluded that the genesis of the Nuri deposit belongs to porphyry-skarn deposit.

Diffusion of Sm-Nd in Scheelite and its Significance to Isotopic Dating and Tracing

As the principal ore mineral in various tungsten(-gold)deposits,scheelite(CaWO_(4))plays an important role in directly dating the timing of ore formation,and in tracing associated material sources through the study of its Sm-Nd geochronology and Nd isotopic characteristics.Since the retention of Sm-Nd systematics within scheelite is presently unconstrained,equivocal interpretations for isotopic data resulting from this method have occurred quite often in previous studies that apply these isotopic data.In order to better elucidate the closure of Sm-Nd in scheelite,the kinetics of Sm and Nd within this mineral lattice were investigated through calculation of diffusion constants presented herein.The following Arrhenius relations were obtained:D_(Nd)=4.00exp(-438 kJ·mol^(–1)/RT)cm^(2)/s D_(Sm)=1.85exp(-427 kJ·mol^(–1)/RT)cm^(2)/s showing diffusion rate of Nd is near identical to Sm in scheelite when at the same temperature.However,compared to other rare earth elements(REEs),which have markedly different atomic radii to either Nd or Sm,these are shown to exhibit a great variation in diffusivities.The observed trends in our data are in excellent agreement with the diffusion characteristics of REEs in other tetragonal ABO4 minerals,indicating that ionic radius is a key constraint to the diffusivity of REEs in the various crystal lattices.With this in mind,the same substitution mechanism and a very slight discrepancy in radii will allow us to infer that significant Sm/Nd diffusional fractionation in scheelite is unlikely to occur during most geological processes.Based upon the diffusion data determined herein,Sm and Nd closure temperatures and retention times in scheelite are discussed in terms of diffusion dynamics.Those results suggest that closure temperatures for Sm-Nd within this mineral are relatively high in contrast to the temperature ranges of ore-formation responsible for scheelite-related deposits,and any later thermal environments.It is likely,therefore,that relevant isotopic information could be easily retained under most geological conditions,since initial crystallization of the scheelite.In addition,comparison of this mineral-element pair over a range of temperatures with some other common minerals used as geochronometers(e.g.,zircon and apatite)indicates that Sm-Nd system has a slower diffusive rate in scheelite than for Sr in apatite or Ar in quartz,and only a little faster than for Pb in zircon.It should be noted,within most hydrothermal deposits where zircon has crystallized,its size is typically no more than 100μm,whereas scheelite commonly occurs as macroscopic grains.For this reason,the larger dimensions of scheelite would provide a robust Sm-Nd system more able to resist perturbations,relating to any later thermal process.As such Sm-Nd investigations of scheelite are akin to U-Pb within zircon samples used in isotopic dating.These observations indicate that Sm-Nd age and isotopic information can provide reliable data in all but the most extreme case,especially when data are extracted from macroscopic grains of scheelite that are chosen to be“pristine”(i.e.,free of surface alteration and/or fractures).

Extensive Resetting of Feldspar Pb Isotopic Composition in Archean–Paleoproterozoic Granitic Rocks from the Kongling Terrane,South China:Implications for Tracing Thermal Evolutionary History

Feldspar Pb isotopes have been widely used to trace magmatic formation and evolution processes.However,it remains unclear whether post-magmatic thermal events can affect feldspar Pb isotopic ratios.Here,the in situ Pb isotopic composition of feldspar hosted in granitic rocks(thirteen Archean and one Paleoproterozoic)from the northern Kongling terrane,Yangtze Craton,South China,is analyzed.The samples reveal a substantial variation in their Pb isotopic composition,spanning the gap between the 1.9 Ga and present-day geochrons,which indicates extensive resetting by later tectonothermal events.This resetting was interpreted to have likely resulted from Paleoproterozoic and Neoproterozoic tectonothermal events related to the assembly and breakup of the Columbia and Rodinia supercontinents.These results suggest that Pb isotopes should be used cautiously when tracing magma sources and petrogenesis in magmatic rocks that have experienced post-magmatic reworking.However,the in situ Pb isotopic composition of feldspar in ancient granitoids may also potentially be used to reveal later tectonothermal events.The extensive resetting of the Pb isotopic composition in feldspar by regional thermal events may also provide new insights into our understanding of the Pb isotope paradox.

Bulk geochemistry,Rb-Sr,Sm-Nd,and stable O-H isotope systematics of the Metzimevin high-grade iron ore deposit,Mbalam iron ore district,southern Cameroon

Bulk geochemistry,Sr,Nd,and O-H isotope systematics are reported for the first time on banded iron formation(BIF)-hosted high-grade iron ore at the northwestern segment of Congo Craton(CC).Located in Mbalam iron ore district,Southern Cameroon,Metzimevin iron ore deposit is a hematite-magnetite BIF system,dominated by SiO_(2)+Fe_(2)O_(3)(97.1 to 99.84 wt%),with low concentrations of clastic elements e.g.,Al_(2)O_(3),TiO_(2),and HFSE,depicting a nearly pure chemical precipitate.The REE+Y signature of the iron deposit displays strong positive Eu anomaly,strong negative Ce anomaly,and chondritic to superchondritic Y/Ho ratios,suggestive of formation by mixed seawater-high temperature hydrothermal fluids in oxidising environment.The^(87)Sr/^(86)Sr ratios of the BIF are higher than the maximum^(87)Sr/^(86)Sr evolution curves for all Archean reservoirs(bulk silicate earth,Archean crust and Archean seawater),indicating involvement of continentally-derived components during BIF formation and alteration.TheƐ_(Nd)(t)(+2.26 to+3.77)and Nd model age indicate that chemical constituents for the BIF were derived from undifferentiated crustal source,between 3.002 and 2.88 Ga.The variable and diverse O and H isotope data(−1.9‰to 17.3‰and−57‰to 136‰respectively)indicate that the Metzimevin iron ore formed initially from magmatic plumes and later enriched by magmatic-metamorphic-modified meteoric fluids.Mass balance calculations indicate mineralisation by combined leaching and precipitation,with an average iron enrichment factor of>2.67 and SiO_(2)depletion factor of>0.99.This is associated with an overall volume reduction of 28.27%,reflecting net leaching and volume collapse of the BIF protholith.

Muscovite^(40)Ar/^(39)Ar isotopic dating of pegmatite veins in the Bieyesamas rare metal deposit in the Altay Mountain,Xinjiang,northwestern China

1.Objective The Altay Orogenic Belt in Xinjiang,China is located in the west of the Central Asian Orogenic Belt and in the transition zone between the Siberian Plate and the Kazakhstan-Junggar Plate,extending approximately 500 km in northern Xinjiang,China(Fig.1a).The Altay Orogenic Belt has undergone two-way accretion of the Paleozoic crust and the Meso-Cenozoic intracontinental orogeny,leading to the formation of large numbers of intermediate-acid intrusions.More than 100000 pegmatite veins have been discovered in the intermediate-acid intrusions,and they constitute an important rare metal metallogenic belt of China(Fig.1b).

Stable Isotopic Signatures of NO3 in Waste Water Effluent and Los Angeles River

A metropolitan city such as Los Angeles (LA) is an ideal study site with a very high population density, and it houses at least 3 treatment plants where sewage is treated preliminarily and then progressing to tertiary treatment before discharging into the LA River. We will gain a better understanding of the water quality in the LA River and the nitrate load in the watershed system by examining the influence of waste water treatment plants (WWTPs). The goal of this study is to pinpoint the exact source of nitrate in the LA River using the isotope signatures. We have selected sampling locations both upstream and downstream of the WWTP. This serves to monitor nitrate levels, aiding in the assessment of treatment plant effectiveness, pinpointing nitrate pollution sources, and ensuring compliance with environmental regulations. The research explores the isotopic composition of NO3 in relation to atmospheric nitrogen and Vienna Standard Mean Ocean Water, shedding light on the contributions from various sources such as manure, sewage, soil organic nitrogen, and nitrogen fertilizers. Specifically, there is a change in the δ15NAir value between the dry and wet seasons. The isotope values in the Tillman WWTP sample changed between dry and wet seasons. Notably, the presence of nitrate originating from manure and sewage is consistent across seasons, emphasizing the significant impact of anthropogenic and agricultural activities on water quality. This investigation contributes to the broader understanding of nitrogen cycling in urban water bodies, particularly in the context of wastewater effluent discharge. The findings hold implications for water quality management and highlight the need for targeted interventions to mitigate the impact of nitrogen-containing compounds on aquatic ecosystems. Overall, the study provides a valuable framework for future research and environmental stewardship efforts aimed at preserving the health and sustainability of urban water resources. This data informs decisions regarding additional treatment or mitigation actions to safeguard downstream water quality and ecosystem health.

Determinant variables on the isotopic values of particulate organic matter in a neotropical floodplain

Particulate organic matter(POM)is an important energy source for aquatic consumers,understanding its origin and composition is essential for understanding the energetic dynamics of aquatic environments.The aim of this study was to analyze the relationship between POM and phytoplankton(isotopic values and chlorophyll concentration)and abiotic variables during dry and rainy seasons.Sampling was conducted in rivers and lagoons in the floodplain of the Upper ParanáRiver.We found a greater difference in ^(δ13)C values of POM between sampling points than between seasons,indicating that the composition of regional sources influences the composition of POM more than dry and rainy seasons.In addition,the concentration of chlorophyll during the dry season was positively correlated with ^(δ13)C values during that rainy period.Additionally,we found a relationship between factors limiting the growth of phytoplankton and ^(δ13)C values of POM,such as phosphate ions,indicating that variables that regulate phytoplankton growth tend to influence the composition of POM in river floodplains.Therefore,maintaining the variables that regulate the phytoplankton community is of fundamental importance for the composition of POM,an important energy source in aquatic environments.

Geochemical and Isotopic Techniques Constraints on the Origin,Evolution,and Residence Time of Low-enthalpy Geothermal Water in Western Wugongshan,SE China

Geothermal resources are increasingly gaining attention as a competitive,clean energy source to address the energy crisis and mitigate climate change.The Wugongshan area,situated in the southeast coast geothermal belt of China,is a typical geothermal anomaly and contains abundant medium-and low-temperature geothermal resources.This study employed hydrogeochemical and isotopic techniques to explore the cyclic evolution of geothermal water in the western Wugongshan region,encompassing the recharge origin,water-rock interaction mechanisms,and residence time.The results show that the geothermal water in the western region of Wugongshan is weakly alkaline,with low enthalpy and mineralization levels.The hydrochemistry of geothermal waters is dominated by Na-HCO_(3)and Na-SO_(4),while the hydrochemistry types of cold springs are all Na-HCO_(3).The hydrochemistry types of surface waters and rain waters are NaHCO_(3)or Ca-HCO_(3).The δD and δ^(18)O values reveal that the geothermal waters are recharged by atmospheric precipitation at an altitude between 550.0 and 1218.6 m.Molar ratios of maj or solutes and isotopic compositions of^(87)Sr/^(86)Sr underscore the significant role of silicate weathering,dissolution,and cation exchange in controlling geothermal water chemistry.Additionally,geothermal waters experienced varying degrees of mixing with cold water during their ascent.Theδ^(13)C values suggest that the primary sources of carbon in the geothermal waters were biogenic and organic.Theδ^(34)S value suggests that the sulfates in geothermal water originate from sulfide minerals in the surrounding rock.Age dating using 3H and^(14)C isotopes suggests that geothermal waters have a residence time exceeding 1 kaBP and undergo a long-distance cycling process.

Morphological and Sulfur-Isotopic Characteristics of Pyrites in the Deep Sediments from Xisha Trough,South China Sea

Pyrite is one of the common authigenic minerals in marine sediments.Previous studies have shown that the morphological and isotopic characteristics of pyrite are closely related to the geochemical environment where it is formed.To better understand the for-mation mechanism of authigenic pyrite,we analyzed the isotopic composition,morphology,and distribution of pyrite in the sediment at 500m below the seafloor from Xisha Trough,South China Sea.Mineral morphologies were observed by scanning electron micros-copy and Raman spectrography.X-Ray computed tomography was applied to measure the particle size of pyrite.The size of pyrite crystals in the matrix sediment mainly ranged between 25 and 65µm(av.ca.40µm),although crystals were larger(av.ca.50μm)in the veins.The pyrites had a fine-grained truncated octahedral shape with occasionally well-developed growth steps,which implies the low growth rate and weak anaerobic oxidation of methane-sulfate reduction when pyrite was formed.Theδ^(34)S values of pyrites ranged from+20.8‰Vienna-defined Canyon Diablo Troilite(V-CDT)to+33.2‰V-CDT and from+44.8‰V-CDT to+48.9‰,which suggest two growth stages.In the first stage,with the continuous low methane flux,the pyrite possibly formed in an environment with good access to seawater.In the second stage,the pyrites mainly developed in sediment fractures and appeared in veins,probably due to the limited availability of sulfate.The less exposure of pyrite to the environment in the second stage was probably caused by sediment accumulation or perturbation.In this study,an episodic pyritization process was identified,and the paleoenvironment was reconstructed for the sediment investigated.

Loggerhead Sea Turtles Hand-Reared in Captivity: Isotopic Insights into Their Inherent Dietary Variation

Stable isotope analysis is a widely used method for gathering ecological insights into the diet and feeding habitats of various species. While captive studies often limit lethal sampling and differ from wild conditions, they offer valuable insights into inherent isotopic variations among individuals, which are often assumed to reflect differences between natural populations. In the Sea Turtle Conservation Program, loggerhead turtle hatchlings from different nests were fed. Necropsies were conducted on turtles that died during this period, obtaining bone fragments for analysis. We evaluated the isotopic variation of carbon (δ13C) and nitrogen (δ15N) in bone tissue across six turtle nests (n = 66 samples) and assessed differences in Straight Carapace Length (SCL, n = 71 samples). Using SIBER and nicheROVER in R, we calculated niche width and overlap, while the simmr package determined primary prey assimilation. Despite feeding the hatchlings the same prey, we observed variations in nitrogen isotope assimilation between nests. Nests 4 and 6 had a niche width >1.8‰, indicating consistent consumption frequencies across all prey and >70% niche overlap with other nests. In contrast, nests 1 and 2 showed a narrower niche width (Mugil sp. constituted the primary diet component (>40%) across all groups. This study demonstrates how factors like competition or prey preference can influence the assimilation of diet, even when the source remains constant (inherent variation).

Hydrogeochemical and isotopic assessment of the origin of NO_(3)^(−)and N-NH_(3)contents in the aquifer located in a closed lacustrine volcano-sedimentary basin in the metropolitan area of Mexico City

To explain the presence and spatial distribution of NO_(3)^(−)and N-NH_(3)in the Aquifer of the Metropolitan Area of Mexico City(AMAMC),a hydrogeochemical and isotopic analysis using^(13)C DIC(as well as the stable isotopes^(18)O and^(2)H)in groundwater was conducted.This aquifer is located in an old closed lacustrine volcano-sedimentary basin;some wells hosted in the semi-confined zone contain high N-NH_(3)concentrations,while others present NO_(3)^(−)contents in the recharge zones(hosted in an oxidizing environment).In this study,a change in the isotopic signature(primarily in^(18)O and^(2)H)was observed from the recharge zones to the basin center in some of the wells with high NO_(3)^(−)concentrations,this behavior can be attributed to evaporation during the incorporation of recently infiltrated water.In addition,the results for^(13)C(along with ^(2) H)in wells with the highest N-NH_(3)concentrations exhibited an atypically broad range of values.Results indicated the occurrence of hydrogeochemical and/or biochemical processes in the aquifer(in an oxidizing or reducing environment),such as organic degradation,bacterial decomposition(primarily in the ancient Lake Texcoco and which acts as a natural sink for carbon,nitrogen,sulfur,and phosphorus),besides rock weathering and dissolution,which may be responsible for a very marked isotopic modification of the^(13)C(and,to a lesser extent,2 H).Methanotrophic bacterial activity and methanogenic activity may be related to N-NH_(3)removal processes by oxidation and residual water incorporation respectively,whereas the increase in the NO_(3)^(−)content in some wells is due to the recent contribution of poor-quality water due to contamination.

A review of ^(17)O isotopic labeling techniques for solid-state NMR structural studies of metal oxides in lithium-ion batteries

Recent advances in utilizing ^(17)O isotopic labeling methods for solid-state nuclear magnetic resonance(NMR)investigations of metal oxides for lithium-ion batteries have yielded extensive insights into their structural and dynamic details.Herein,we commence with a brief introduction to recent research on lithium-ion battery oxide materials studied using ^(17)O solid-state NMR spectroscopy.Then we delve into a review of ^(17)O isotopic labeling methods for tagging oxygen sites in both the bulk and surfaces of metal oxides.At last,the unresolved problems and the future research directions for advancing the ^(17)O labeling technique are discussed.

Characteristics of carbon isotopic composition of alkane gas in large gas fields in China

Exploration and development of large gas fields is an important way for a country to rapidly develop its natural gas industry.From 1991 to 2020,China discovered 68 new large gas fields,boosting its annual gas output to 1925×108m3in 2020,making it the fourth largest gas-producing country in the world.Based on 1696 molecular components and carbon isotopic composition data of alkane gas in 70 large gas fields in China,the characteristics of carbon isotopic composition of alkane gas in large gas fields in China were obtained.The lightest and average values ofδ^(13)C_(1),δ13C2,δ13C3andδ13C4become heavier with increasing carbon number,while the heaviest values ofδ^(13)C_(1),δ13C2,δ13C3andδ13C4become lighter with increasing carbon number.Theδ^(13)C_(1)values of large gas fields in China range from-71.2‰to-11.4‰(specifically,from-71.2‰to-56.4‰for bacterial gas,from-54.4‰to-21.6‰for oil-related gas,from-49.3‰to-18.9‰for coal-derived gas,and from-35.6‰to-11.4‰for abiogenic gas).Based on these data,theδ^(13)C_(1)chart of large gas fields in China was plotted.Moreover,theδ^(13)C_(1)values of natural gas in China range from-107.1‰to-8.9‰,specifically,from-1071%o to-55.1‰for bacterial gas,from-54.4‰to-21.6‰for oil-related gas,from-49.3‰to-13.3‰for coal-derived gas,and from-36.2‰to-8.9‰for abiogenic gas.Based on these data,theδ^(13)C_(1)chart of natural gas in China was plotted.

Sm-Nd ISOTOPIC SYSTEMATICS OF THE NE JIANGXI OPHIOLITE(NEJXO), SE MARGIN OF THE YANGTZE CRATON, SOUTH CHINA

The ophiolite belt along the S.E. margin of the Yangtze craton(or platform), South China is commonly considered to be formed during the Sibao-Xuefeng orogenic cycle and interpreted to represent a Proterozoic suture or subduction zone. In contrast, Hsu et al. recently argued that this ophiolite belt represented a melange which was overthrust onto a foreland thrust belt during Mesozoic. To resolve this conflict and obtain better under-

Apatite Geochemical and Nd Isotopic Insights into Trachyte Petrogenesis in the Tianchi Volcanic Area of Changbai Mountain,NE China

We report the oxide,element geochemistry and Nd isotopic geochemical data of apatite in the middle Pleistocene medium-and fine-grained trachyte in the Tianchi volcanic area(TVA)of Changbai Mountain,discussing the relationship between apatite and the composition of the whole rock.The purpose is to use the apatite geochemical data to constrain the evolutionary process of trachytic magma and the petrogenesis of trachyte in the cone-forming period of the Tianchi volcano.Apatite(Ca_(5)(PO_(4))_(3)(OH,F,Cl))is a common accessory mineral that occurs widely in volcanic rocks in the TVA.The apatites in the trachyte are mainly subhedral-anhedral,having the characteristics of magmatic apatite.In terms of oxide and element geochemistry,they have homogeneous Al_(2)O_(3),SiO_(2),MgO,P_(2)O_(5),K_(2)O,CaO and heterogeneous TiO2,with high F content.They are generally enriched in Th,U and LREEs,depleted in Nb,Ta,Zr,Hf and HFSEs,showing negative Ba,Sr and Ti anomalies,similar to those of the whole-rock host trachytes.The ratios of high(La/Yb)_(N),low δEu(Eu/Eu*),Sr/Y value and ΣREE content in apatite,and the F,Sr,Y,Th/U,La/Sm,and Nd/Tb with ΣREE andδEu anomalies showed a linear correlation,all of those indicating that the host magma has the characteristic of high differentiation.The apatite grains generally having ^(147)Sm/^(144)Nd,^(143)Nd/^(144)Nd ratios and ε_(Nd)(t)values of 0.1072-0.1195,0.5123-0.5126 and -3.49 to -0.10,respectively,are similiar to those of the host rock.The Nd model ages TDM1 are 949-803 Ma in apatite.Combined with theεNd(t)value of the apatite core(-7.06 to-3.49),we conclude that the initial magma of the host trachyte was derived from the partial melting of Proterozoic crustal material and there was an assimilation of wall rocks during its evolution.

Rare earth elemental and Sr isotopic evidence for seawater intrusion event of the Songliao Basin 91 million years ago

Petrogenesis of lacustrine dolostone is closely related with paleo-lake water conditions.Here we report the high spatial-resolution petrographic and geochemical results of a lacustrine dolomite nodule from the Qingshankou Formation,the Songliao Basin.Sedimentary and elemental signatures confirm the protogenetic origin of this nodule and its effectiveness in recording geochemical characteristics of paleo-lake water during dolomitization.The low Y/Ho ratios,middle rare earth element(MREE)enrichment and subtle positive Eu anomalies within the nodule indicate a fresh water source.However,the Sr isotope values in the core of the nodule(0.7076-0.7080)are close to contemporaneous seawater(0.7074),yet different from the modern river(0.7120)and the host black shale(0.7100).On the premise of excluding the influence of hydrothermal fluids,the significantly low strontium isotope values of the lacustrine dolomite might be caused by seawater interference during dolomitization.Our findings demonstrate that lacustrine dolomite within black shales is not only a faithful tracer of diagenetic water environment,but also a novel and easily identified mineralogical evidence for episodic seawater intrusion event(91 Ma)in the Songliao Basin,which supplements other paleontological and geochemical evidence.

Decoupling of Lu-Hf and Sm-Nd Isotopic System in Deep-Seated Xenoliths from the Xuzhou-Suzhou Area,China: Differences in Element Mobility during Metamorphism

This paper presents whole-rock Hf isotopic data for a suite of eclogite and garnet clinopyroxenite xenoliths hosted in the Early Cretaceous dioritic intrusions from the Xuzhou-Suzhou area along the southeastern margin of the Eastern Block of the North China Craton(NCC).Six of the eight studied xenolith samples plot significantly above the terrestrial Hf-Nd isotopic array and haveεHf(0)value up to+60.All the samples define a well correlated 147 Sm/144 Nd-143 Nd/144 Nd age of 2081 Ma,which is considered to record the granulite-facies metamorphism.In contrast,the Lu-Hf isotope system faithfully records the protolith information.The mineralogical assemblage,especially garnet and/or zircon(rutile to some extent)mainly controlled the decoupling of Hf-Nd isotope.The metamorphic modification on protolith characteristics and the differences in element mobility during metamorphism may also reinforce the observed decoupling between the Sm-Nd and Lu-Hf isotope systems;i.e.,the absence of the correlations inεNd-εHf and also 87 Sr/86 Sr-143 Nd/144 Nd diagram.The Lu/Hf isochron age of 2424 Ma is similar to the zircon age peak of the studied xenoliths and the dominant age of NCC basement,indicating that the igneous protolith has an affinity to the Archean basement of the NCC.Furthermore,the positiveεHf(t)values at 2500 Ma indicate a crustal growth event of 2500 Ma in the NCC.

Rising utilization of stable isotopes in tree rings for climate change and forest ecology

Analyses of stable isotopes(C,O,H)in tree rings are increasingly important cross-disciplinary programs.The rapid development in this field documented in an increasing number of publications requires a comprehensive review.This study includes a bibliometric analysis-based review to better understand research trends in tree ring stable isotope research.Overall,1475 publications were selected from the Web of Science Core Collection for 1974-2023.The findings are that:(1)numbers of annual publications and citations increased since 1974.From 1974 to 1980,there were around two relevant publications per year.However,from 2020 to 2022,this rose sharply to 109 publications per year.Likewise,average article citations were less than four per year before 1990,but were around four per article per year after 2000;(2)the major subjects using tree ring stable isotopes include forestry,geosciences,and environmental sciences,contributing to 42.5%of the total during 1974-2023;(3)the top three most productive institutions are the Chinese Academy of Sciences(423),the Swiss Federal Institute for Forest,Snow and Landscape Research(227),and the University of Arizona(204).These achievements result from strong collaborations;(4)review papers,for example,(Dawson et al.,Annu Rev Ecol Syst 33:507-559,2002)and(McCarroll and Loader,Quat Sci Rev 23:771-801,2004),are among the most cited,with more than 1000 citations;(5)tree ring stable isotope studies mainly focus on climatology and ecology,with atmospheric CO_(2) one of the most popular topics.Since 2010,precipitation and drought have received increasing attention.Based on this analysis,the research stages,key findings,debated issues,limitations and direc-tions for future research are summarized.This study serves as an important attempt to understand the progress on the use of stable isotopes in tree rings,providing scientific guid-ance for young researchers in this field.

Origin of hydrocarbon fluids and discussion of abnormal carbon isotopic compositions in the Lishui-Jiaojiang Sag,East China Sea Shelf Basin

The hydrocarbon gases in the L1 gas field of the Lishui-Jiaojiang Sag have been commonly interpreted to be an accumulation of pure sapropelic-type thermogenic gas.In this study,chemical components,stable isotopic compositions,and light hydrocarbons were utilized to shed light on the origins of the hydrocarbon fluids in the L1gas pool.The hydrocarbon fluids in the L1 gas pool are proposed to be a mixture of three unique components:mid-maturity oil from the middle Paleocene coastal marine Lingfeng source rock,oil-associated(late oil window)gas generated from the lower Paleocene lacustrine Yueguifeng source rock,and primary microbial gas from the paralic deposits of the upper Paleocene Mingyuefeng source rock.Here,for the first time,the hydrocarbon gases in the L1 gas pool are diagnosed as mixed oil-associated sapropelic-type gas and microbial gas via four pieces of principal evidence:(1)The abnormal carbon isotopic distributions of all methane homologues from C_(1)(CH_(4)or methane)to C_(5)(C_(5)H_(12)or pentane)shown in the Chung plot;(2)the diagnostic~(13)C-depleted C_(1)compared with the thermogenic sapropelic-type gas model,whileδ^(13)C_(2)(C_(2)H_(6)or ethane)andδ^(13)C_(3)(C_(3)H_(8)or propane)both fit perfectly;(3)the excellent agreement of the calculated carbon isotopic compositions of the pure thermogenic gas with the results of the thermal simulated gas from the type-II1 kerogen-rich Yueguifeng source rock;and(4)the oil-associated gas inferred from various binary genetic diagrams with an abnormally elevated gas oil ratio.Overall,the natural gases of the L1 gas pool were quantified in this study to comprise approximately 13%microbial gas,nearly 48%oil-associated sapropelic-type gas,and 39%of nonhydrocarbon gas.The microbial gas is interpreted to have been codeposited and entrained in the humic-kerogen-rich Mingyuefeng Formation under favorable lowtemperature conditions during the late Paleocene-middle Eocene.The microbial gas subsequently leaked into the structurally and stratigraphically complex L1 trap with oil-associated sapropelic-type gas from the Yueguifeng source rock during the late Eocene-Oligocene uplifting event.A small amount of humic-kerogen-generated oil in the L1 gas pool is most likely to be derived from the underlying Lingfeng source rock.The detailed geological and geochemical considerations of source rocks are discussed to explain the accumulation history of hydrocarbon fluids in the L1 gas pool.This paper,therefore,represents an effort to increase the awareness of the pitfalls of various genetic diagrams,and an integrated geochemical and geological approach is required for hydrocarbonsource correlation.