Boron Isotopic Composition of Halite from 46-m-long Sediment Core in the Qarhan Salt Lake,Western China

Previous studies have investigated the boron isotopic composition of salt lake brines in the Qaidam Basin,western China.However,the research on boron isotopic composition of halite is very limited due to halite’s low

Boron isotopic variations in tourmaline from metacarbonates and associated calc-silicate rocks from the Bohemian Massif: Constraints on boron recycling in the Variscan orogen

Various metacarbonate and associated calc-silicate rocks form minor but genetically significant components of the lithological units in the Bohemian Massif of the Variscan orogen in Central Europe.These rocks vary in terms of their lithostratigraphy,chemical composition and mineral assemblage(dolomite/calcite ratio,silicate abundance).Tourmaline is present in five paragenetic settings within the metacarbonate and calc-silicate units.TypeⅠcomprises individual,euhedral,prismatic grains and grain aggregates in a carbonate-dominant(calcite±dolomite)matrix poor in silicates.TypeⅡis characterized by euhedral to subhedral grains and coarse-to fine-grained aggregates in silicate-rich layers/nests within metacarbonate bodies whereas typeⅢoccurs as prismatic grains and aggregates at the contact zones between carbonate and associated silicate host rocks.TypeⅣis in veins crosscutting metacarbonate bodies,and typeⅣtourmaline occurs at the exocontacts of elbaite-subtype granitic pegmatite.Tourmaline from the different settings shows distinctive compositional features.Typical for typeⅠare Mg-rich compositions,with fluor-uvite>dravite>>magnesio-lucchesiite.Tourmalines from typeⅡsilicate-rich layers/nests are highly variable,corresponding to oxy-schorl,magnesio-foitite,Al-rich dravite and fluor-uvite.Typical for typeⅢtourmalines are Ca,Ti-bearing oxy-dravite compositions.The typeⅣveins feature dravite and fluor-uvite tourmaline compositions whereas typeⅤtourmaline is Li,F-rich dravite.Tourmaline is the only Bbearing phase in paragenetic typesⅠ-Ⅳ,where it is characterised by two principal ranges of B-isotope composition(δ^11B=-13‰to-9‰and-18‰to-14‰).These ranges correspond to regionally different units of the Moldanubian Zone.Thus,the Svratka Unit(Moldanubian Zone s.l.)contains only isotopically lighter tourmaline(δ^11B=-18‰to-14‰),whereas metacarbonates in the Poli?ka unit(Teplá-Barrandian Zone)and Olesnice unit(Moravicum of the Moravo-Silesian Zone)has exclusively isotopically heavier tourmaline(δ^11B=-9‰to-13‰).Tourmalines from metacarbonates in the Variegated Unit cover both ranges of isotope composition.The isotopically light end of the B isotope range may indicate the presence of continental evaporites within individual investigated areas.On the other hand,variations in the range of~8δ-units is consistent with the reported shift in B isotopic composition of metasedimentary rocks of the Bohemian Massif due to the prograde metamorphism from very-low grade to eclogite facies.In contrast to the metacarbonate-hosted settings,tourmaline of paragenetic type V from the exocontact of granitic pegmatites displays a significantly heavier range ofδ^11B(as low as-7.7‰to-0.6‰),which is attributed to partitioning of 10 B to cogenetic axinite and/or different B-signature of the source pegmatite containing tourmaline with heavyδ^11B signature.

Geochemical and Boron Isotopic Evidence that Tourmaline Records Country Rock Assimilation of Leucogranites in the Himalayan Orogen

Tourmaline geochemical and boron(B)isotopic compositions in two-mica granites(TMG),tourmaline-bearing leucogranites(Tou-LG),tourmalites and metapelites from the Gyirong-Malashan areas of the Himalayan orogen provide evidence for country rock assimilation during the intrusion of Himalayan leucogranite.The schorls in Gyirong leucogranitic plutons show low contents of MgO(0.238%-1.160%)and δ^(11)B values(-12.1‰--11.2‰),while dravites gathered in the contact zone between the leucogranitic veins and metapelites show high contents of MgO(4.815%-6.755%)and δ^(11)B values(-10.7‰--9.3‰).This geochemical and isotopic variation of tourmalines can also be identified in the Malashan gneiss dome.As a result,three types of tourmaline were identified in the Himalayan orogen:(1)Tou-Ⅰ in the TMG and Tou-LG,which is the most common tourmaline type of schorl;(2)Tou-Ⅱ(dravite and high-Mg schorl)in the Tou-LG and tourmalite at the margins of the leucogranite;and(3)Tou-Ⅲ(mainly dravite,with minor high-Mg schorl)in metapelites of the High Himalayan Crystalline Sequence.The lenses and veins of Tou-LG may have experienced metasomatism and assimilation as a result of interaction with the High Himalayan Crystalline Sequence metasedimentary country rocks,which can be traced by the geochemical and isotopic characteristics of the tourmaline therein.

The source of lithium in Lakkor Co Salt Lake on Qinghai-Tibet Plateau,China:evidence from hydrochemical characteristics and boron isotope

The availability of lithium resources is of great significance for the development of modern technologies,as well as for civil and military industries.The Qinghai-Tibet Plateau is a region known for its abundance of lithium-rich salt lakes.However,the specific origin of lithium in these lakes is still unknown,which hinders the advancement of the lithium resource business in this region.To research this issue,this study involved the collection of 20 samples from Lakkor Co Salt Lake on Qinghai-Tibet Plateau,encompassing samples of surface brine,cold springs,fresh lakes,and recharge rivers.The composition of anions and cations in these samples was determined.Furthermore,the analysis extensivelyutilizedthePiperthree-linediagram,Gibbs model,and ion proportion coefficient.The findings of this study indicate that as the moves from the recharge water system to salt lake,there is a transition in water type from strong carbonate to moderate carbonate and weak carbonate,as well as Na sulfate.This research based on a similar source of both lithium and boron,utilized ion correlation analysis and boron isotope study in the Lakkor Co area,and analyzed the source and transporting process of lithium.The main origin of lithium in Lakkor Co is the dissolution of lithiumrich rocks,recharge water systems,and deep hydrothermal fluids.These findings are highly significant in enhancing the foundational data of lithium-rich brine resources in the Qinghai-Tibet Plateau and are beneficial for assessing the future development of such deposits.

Boron Isotopic Fractionation and Trace Element Incorporation in Various Species of Modern Corals in Sanya Bay, South China Sea

The boron isotope paleo-pH proxy has been extensively studied due to its potential for understanding past climate change, and further calibrations were considered for accurate applications of the proxy because of significant variability related to biocarbonate microstructure. In this work, we studied the boron isotopic fractionation between modern marine corals and their coexisting seawater collected along shallow area in Sanya Bay, South China Sea. The apparent partition coefficient of boron（KD） ranged from 0.83×10-3 to 1.69×10-3, which are in good agreement with previous studies. As the analyzed coral skeleton（~5 g） spanned the growth time period of 1–2 years, we discussed the boron isotopic fractionation between pristine corals and modern seawater using the annual mean seawater pH of 8.12 in this sea area. Without taking the vital effect into account,（11B/10B）coral values of all living corals spread over the curves of（11B/10B）borate vs.（11B/10B）sw with the α4-3 values ranging from 0.974 to 0.982. After calibrating the biological effect on the calcifying fluid pH, the field-based calcification on calcifying fluid pH（i.e., Δ（pHbiol-pHsw）） for coral species of Acropora, Pavona, Pocillopora, Faviidae, and others including Proites are 0.42, 0.33, 0.36, 0.19, respectively, and it is necessary to be validated by coral culturing experiment in the future. Correlations in B/Ca vs. Sr/Ca and B/Ca vs. pHbiol approve temperature and calcifying fluid pH influence on skeletal B/Ca. Fundamental understanding of the thermodynamic basis of the boron isotopes in marine carbonates and seawater will strengthen the confidence in the use of paleo-pH proxy as a powerful tool to monitor atmospheric CO2 variations in the past.

Boron isotopic composition of Paleozoic brachiopod and coeval coral calcites in Yunnan-Guizhou Plateau, China

Boron isotope values in Paleozoic brachiopods and corals, collected from the Yunnan-Guizhou Plateau, China, can be used to constrain the boron isotope compositions of past oceans. All brachiopod shells and coral samples were screened for diagenetic recrystallization by cathodoluminescence microscopy, trace element geochemistry of B, Fe, Mn, Sr, and scanning electron microscopy. The boron isotope ratios for brachiopods in Silurian, Devonian, Carboniferous, and Triassic calcites are in the ranges 8.9‰-14.0‰, 8.8‰-13.8‰, 10.3‰-16.3‰, and 6.7‰-12.4‰, respectively. The boron isotope ratios of coral calcites in the Silurian, Devonian, and Permian are 9.1‰-12.2‰, 6.1‰-13.8‰, and 9.2‰-16.1‰, respectively. The δ11B values for both brachiopods and corals are significantly lower than those for modern biogenic carbonates, indicating that the Paleozoic oceans were depleted of δ11B by up to 10‰. Our results are consistent with previous published studies. The boron isotope compositions of corals and brachiopods show the consistent trends. The low δ11B values may be explained by an enhanced riverine flux of boron from the continents.

Boron isotope geochemistry of Zigetang Co saline lake sediments,Tibetan Plateau

The origin of boron in boron-rich salt lakes in the Tibetan Plateau is highly controversial.In this study,we carried out a detailed study on boron geochemistry and isotope composition of lake sediments collected in Zigetang Co,central Tibet.Evaporites had high boron concentrations of 172.3–418.6 lg/g and δ^(11)B values of-8.2%to-3.3%,suggesting a non-marine origin for the saline lake.The boron isotopic fractionation factor,a,between evaporite and brackish water(a_(evaporite–brackish))decreased systematically with depth,from 0.9942 at the top of the drill core to 0.9893 at the bottom;the linear variation between α_(evaporite–brackish)and depth reflects boron isotopic fractionation associated with progressive crystallization.The positive correlation between δ^(11)B versus[B]and δ^(11)B versus depth in the evaporite phase reflects pH and boron speciation in the solution control on the adsorption of boron,and B(OH)_3 species incorporated preferentially into Mg(OH)_2 precipitation at high pH.

Boron isotope geochemistry of Bangor Co Salt Lake(central Tibet):implications for boron origin and uneven mixing of lake water

Boron is an essential,widely used,micronutrient element and is abundant in salt lakes on the Qinghai-Tibet Plateau.The origin and distribution of boron brine deposits on the Qinghai-Tibet Plateau is an important foundation for B resource formation,evolution,and enrichment,which have long been the subject of debate.The boron isotope system is a sensitive geochemical tracer,making it useful for eff ectively and precisely tracking a wide range of geological processes and sources.This study investigates the major cations,[B],andδB values of samples(lake brine,river waters,and cold spring water)from the Bangor Co Lake which is a typical salt lake rich in boron in Tibet,China.There are magnitude-scale diff erences in[B]among diff erent sample types:river samples<cold spring water<<brine lakes.[B]values vary from 0.73 to~1113 mg/L.Similar to[B],theδB values of the samples exhibit magnitude-scale variations as[B],ranging from-7.35‰to+7.66‰.There are also magnitude-scale diff erences inδB among diff erent sample types.TheδB values of cold spring water are relatively low,and the values range from-1.26‰to-7.75‰.However,the river water samples and saline lakes have higher values,from 0.38‰to 4.62‰,and theδB values of river water samples are basically in the distribution range of those of Bangor Co Lake.This indicates that the sources of boron in Bangor Co Lake are mainly the recharge water with higherδB values and spring water with lowerδB values,and the boron sources and the uneven mixing of lake water are two reasons that account for the large change in theδB value of Bangor Co Lake.

Chronology and Genesis of S-type Granites in Hetai District, Guangdong Province: Constraints from LA-ICP-MS Zircon U-Pb Dating and Tourmaline Boron Isotope In-situ Analyses

1 Introduction Hetai district,which is a mountainous area,situated on Guangning and Zhaoqing city,west Guangdong Province.Hetai district is generally located on southwest of South China Caledonian fold belt,east margin of Yunkai post-Caledonian uplift.Multiple type granites are widely distributed in Hetai district,including Caledonian,Indosinian and Yanshanian granites.Based on different

Problems of Lithium Isotope Research in Salt Lake Study

Lithium in nature mainly exists in the forms of solid minerals and ionic liquid.More than 150 lithium minerals exist,which are mainly pegmatite mineral including triphane,lithionite and petalite.Liquid lithium mainly

A preliminary experimental study of the boron concentration in vapor and the isotopic fractionation of boron between seawater and vapor during evaporation of seawater

A laboratory experiment was undertaken to investigate the behaviour of boron at the seawater-air interface under air flow conditions. Dried air at 25 and 35℃ was passed over or bubbled through seawater at the same temperature. A combination of ice-chilled condensers and KOH impregnated cellulose fibre filters was used to collect boron from the reacted air. When air stripped of boron was passed over the seawater, boron was found in the reacted air, and its concentration was higher in the higher temperature test. In the tests where air was bubbled through seawater the concentration of boron in the reacted air was directly proportional to the air flow rate. In this situation the boron in the reacted air was mainly introduced as a spray of microdroplets. Isotopic analysis of the collected boron in the non-bubbled tests yields fractionation factors which demonstrate that the lighter isotope, 10B, is enriched in the reacted air. The size of the fractionation changes with temperature, ruling out a purely kinetic effect.

A Multi–fluid Constrain for the Forming of Potash Deposits in the Savannakhet Basin: Geochemical Evidence from Halite

The Khorat Plateau on the Indochina Terrane is known to have formed during the closure of the Tethys Ocean, although the origin of its potash mineral deposits is a topic of current debate. Data from a borehole on Savannakhet Basin is used in this study to re-define the evaporation processes of the study area. Geochemical analyses of halite from various borehole-derived evaporite strata have elucidated the fluid sources from which these ores formed. Measured δ11B indicated that ore deposits formed primarily due to evaporation of seawater, although non-marine fluids affected the later stages of the evaporation process. Fluctuations in B and Br concentrations in carnallite- and sylvite-rich strata indicate the influence of fresh water. Boron concentration in carnallite unit indicated the influence of hydrothermai fluids. From the relative timings of these various fluid influxes, the evolution of these evaporates can be divided into four stages： （1） an initial marine evaporation at the beginning of the deposit＇s formation, where seawater （and minor fresh water） trapped on the uplifted Khorat Plateau produced sediments and salts with Br contents lower than those of normal marine-derived evaporites; （2） a transgression stage, where seawater recharged the basin; （3） a hydrothermal infiltration stage, which was coeval with the late Yanshan movement; and （4） a stage of fresh water supply, as recorded by fluctuations in B and Br contents, inferring intermittent fresh water influx into the basin. Thus, although evaporites on the Savannakhet Basin primarily formed via marine evaporation, they were also influenced to a significant degree by the addition of non-marine fresh water and hydrothermal fluids.

Proto-Adamastor ocean crust(920 Ma)described in Brasiliano Orogen from coetaneous zircon and tourmaline

Proto-Adamastor ocean bathed Rodinia and successor continental fragments from 1.0-0.9 Ga up to0.75 Ga,and evolved into world Adamastor Ocean at 0.75-0.60 Ga.Mesoproterozoic oceanic crust is poorly preserved on continents,only indirect evidence registered in Brasiliano Orogen.We report first evidence of ophiolite originated in proto-Adamastor.We use multi-technique U-Pb-Hf zircon andδ^11B tourmaline isotopic and elemental compositions.The host tourmalinite is enclosed in metaserpentinite,both belonging to the Bossoroca ophiolite.Zircon is 920 Ma-old,εHf(920 Ma)=+12,HfTDM=1.0 Ga and has’oceanic’composition(e.g.,U/Yb<0.1).Tourmaline is dravite withδ^11B=+1.8‰(Tur 1),0‰(Tur 2),-8.5‰(Tur 3).These characteristics are a novel contribution to Rodinia and associated world ocean,because a fragment of proto-Adamastor oceanic crust and mantle evolved at the beginning of the Brasiliano Orogen.

Geochemical study of boron isotopes in the process of loess weathering

In this paper the boron contents and boron isotopic composition ofacid-soluble phases in loess and paleosol samples are determined for the first time. The boroncontents of acid-soluble phases in the Luochuan loess section (S_0—S_2) vary within the range of(0.8—2.7)x10^(-6) and their δ^(11)B values vary from -1.8 per thousand to +18.6 per thousand,mostly within the range of 0—+10 per thousand. The boron contents and δ^(11)B values of paleosollayers are higher than those of loess layers, especially in the loess layer S_1. Varying chemicalweathering intensity and loess adsorption capability are the main factors leading to the variationsof boron contents and δ^(11)B values of acid-soluble phases in the loess section. The variation ofchemical weathering intensity in response to the variation of climatic conditions seems to be themain factor leading to the variations of boron contents and δ^(11)B values of acid-soluble phasesin the loess section.

Geochemical processes and origin of boron isotopes in geothermal water in the Yunnan-Tibet geothermal zone

Boron concentrations and isotope compositions have been measured for 93 water samples from the hot springs and drill-holes in the geothermal system in the Yunnan-Tibet Geothermal Belt(YTGB),China.Boron concentrations range from 0.036–472.4ppm,and theδ11B values range from -16.0‰to 13.1‰,indicating the non-marine origin for each geothermal system.We observed a clear binary mixing relationship between the B concentrations and B isotope compositions in Tibet geothermal area.This relationship can be well explained by two sources,i.e.,marine carbonate rocks and magmatic rocks,for the Tibet geothermal water.No evidence supports a mantle contribution to B.In addition,we found that the precipitation only plays a dilution role for B of geothermal waters.δ11B values for the precipitation across the southern Tibetan Plateau area range from -6.0‰ to -6.8‰at least.Due to data scarcity in Yunnan geothermal area,we observed possible different boron sources from the Tibet geothermal system.Comparing it with other geothermal systems in the world,we found that the samples from YTGB have the lowestδ11B values and the largest range of B concentration,which might be related to their special geological background.On the whole,the world geothermalδ11B-Cl/B relation suggests a mixing process between marine and non-marine sources.Additionally,we suggest that B source of B-enriched geothermal waters is mainly from B-enriched crustal country-rocks,instead of mantle.

Separation characteristics of boron isotopes in continuous annular chromatography

A well designed continuous annular chromatograph （CAC） column was set to stndy the enrichment of Boron isotopes. The column is 820 mm high and consists of a rotational annulus with an outer diameter of 246 mm and a width of 15 mm. The weak basic resin （Diaion WA21J）, the boric acid and water were used as the absorbent, the feed and the eluent respectively. The effects of CAC rotating speed, concentration of boric acid and flow ratio of eluent to feed on the enrichment of 10B were investigated. The concentration of boron isotope was determined by a Thermal Elemental X7 ICP-MS （Thermo Electron Co., USA）. It is shown from the experimental results that 10B and 11B can be separated effectively by this CAC column. By fitting the experimental elution profiles based on reliable mathematic models and software the mass transfer coefficient k and adsorp- tion equilibrium constant K values of 10B and 11B in CAC column were estimated. It is clear from this study that the CAC has practical continuous operational capabilities in comparison with fixed batch chromatography and is an effective technology for seoarating boron isotones.

Petrogenesis of granitic pegmatite veins:Perspectives from major element and B isotope in tourmalines,Chakabeishan,Northern Tibetan Plateau

The petrogenesis of regionally zoned granitic pegmatite veins remains debated.Because of the economic significance,we carried out a study on the Chakabeishan(CKBS)pegmatite-type Li-Be deposit,eastern North Qaidam Tectonic Belt,Northern Tibetan Plateau,by means of in-situ major element and B isotope compositions of tourmalines in the beryl-bearing and spodumene-bearing pegmatite veins.Tourmalines(Tur-Be)from the beryl-bearing pegmatite are homogeneous schorl with low Mg/(Mg+Fe),high Na/(Na+Ca)and Y Al,suggesting that they are of magmatic origin.Two generations of tourmalines(TurLi)from the spodumene-bearing pegmatite are identified:(i)the crystal cores(mostly elbaite and Lirich schorl with subordinate schorl)are consistent with being of magmatic origin crystallized at the magmatic stage;(ii)the crystal rims(schorl)are best understood as the overgrowth at the later hydrothermal stage.Tur-Be and Tur-Li show an obvious difference in core-to-rim B isotopic variation trend with d11B decrease in Tur-Be and increase in Tur-Li.The core-to-rim d11B decrease in Tur-Be results from degassing during its host pegmatitic melt evolution,whereas the core-to-rim d11B increase in Tur-Li is related to fluid exsolution.The estimated d11B values for the initial melts of the beryl-bearing and spodumenebearing pegmatites are10.46‰and10.78‰,respectively,indicating that they most likely originate from protracted fractional crystallization/differentiation of granitic intrusions rather than partial melting of metapelite.Both Mg/(Mg+Fe)ratios and Li abundances in the cores of Tur-Be are lower than those of Tur-Li,suggesting that Tur-Li crystallizes from chemically more evolved melts.

Two-neutron halo state of ^(15)B around 3.48 MeV by a three-body model

We investigate low-lying bound states of the neutron-rich nucleus ^15B by assuming it is a three-body system made of an inert core 13 B and two valence neutrons. The three-body wave functions are obtained using the Faddeev formalism. Special attention is paid to the excited state at 3.48（6） MeV observed in the 13 C（14 C,12 N）15 B reaction, whose properties are less clear theoretically. In our three-body model, besides the ground state 3/21, a second 3/22^-state is discovered at around 3.61 MeV, which might be identified with the excited state observed at3.48（6） MeV. We study this 3/22^-state in detail. It turns out to be a two-neutron halo state with a large matter radius rm≈4.770 fm. ＆nbsp

The neutron halo structure of ^(17)B studied with the relativistic Hartree-Bogoliubov theory

The properties of neutron-rich boron isotopes are studied in the relativistic continuum Hartree-Bogoliubov theory in coordinate space with NL-SH,PK1 and TM2 effective interactions.Pairing corrections are taken into account by a density dependent force of zero range.The binding energies calculated for these nuclei agree with the experimental data quite well.The neutron-rich nucleus 17 B has been predicted to have a two-neutron halo structure in its ground state.The halo structure of 17 B is reproduced in a self-consistent way,and this halo is shown to be formed by the valence neutron level 2s 1/2.