Boron isotope variations in nature: a synthesis

The large relative mass difference between the two stable isotopes of boron, ¹⁰B and ¹¹B, and the high geochemical reactivity of boron lead to significant isotope fractionation by natural processes. Published ¹¹B values (relative to the NBS SRM-951 standard) span a wide range of 90. The lowest ¹¹B values around — 30 are reported for non-marine evaporite minerals and certain tourmalines. The most ¹¹B-enriched reservoir known to date are brines from Australian salt lakes and the Dead Sea of Israel with ¹¹B values up to +59. Dissolved boron in present-day seawater has a constant world-wide ¹¹B value of + 39.5. In this paper, available ¹¹B data of a variety of natural fluid and solid samples from different geological environments are compiled and some of the most relevant aspects, including possible tracer applications of boron-isotope geochemistry, are summarized.

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Résumé La grande différence relative de masse entre les isotopes stables du bore, ¹⁰B et ¹¹B, et la grande réactivité geochimique du bore ont pour conséquence un fractionnement isotopique naturel important. Les valeurs de ¹¹B publiées (par rapport au standard NBS SRM-951) varient de 90. Les valeurs de ¹¹B les plus basses (–30) correspondent aux evaporites non-marines et à certaines tourmalines. Le réservoir le plus enrichi en ¹¹B est représenté par les saumures des lacs salés d' Australie et par la Mer Morte en Israël, qui ont des valuers de ¹¹B allent jusqu'à + 59. L'eau de mer a une valeur de ¹¹B mondialement constante de + 39.5. Des valeurs de ¹¹B des solutions naturelles ainsi que des roches et minéraux de différentes origines, publiées jusqu'à présent, sont présentées ici. En outre quelques aspects importants concernant la géochimie des isotopes du bore y compris quelques applications sont exposés.

     

江西省安福地区地热水化学特征研究

为研究江西安福地区水文地球化学特征及控制因素, 本文采集了15组样品, 采用水化学、同位素分析等方法进行研究。结果表明: 研究区地热水以Na-HCO3型水为主, 地下水以HCO3-Na·Ca型为主, 地表水由西南向东北从HCO3-Na·Ca向HCO3-Ca型水演化。水化学组分演化过程主要受岩石风化作用控制, 地层封闭性较差, 水中的Na+、HCO– 3、Sr2+来源于硅酸岩风化溶解。由稳定同位素特征可知, 研究区地热水补给来源为大气降水。研究区热储温度为49.8~101.4 ℃, 地热水循环深度为1 502.6~1 513.6 m。热水在沿断裂带上升过程中与浅层冷水发生混合, 其混合比例为76.1%~87.5%。研究成果为安福地区水循环演化提供依据, 有利于地热资源的合理开采与保护。     

Fe-Cu-Zn-Mo同位素示踪氧化还原过程

非传统稳定同位素（Fe-Cu-Zn-Mo）理论与数据相结合提高了科研工作者对地质体系氧化还原过程的理解。本文对这一相对较新的领域进行了综述,包括与氧化还原过程相关的同位素分馏理论和实验约束、时空尺度下的氧逸度以及同位素示踪氧化还原过程。稳定同位素理论预测,Fe-Cu-Zn-Mo同位素应该对氧化还原状态的变化能够做出响应。结果表明,Fe同位素作为岩浆过程、表生过程、俯冲带流体性质"氧逸度计"应用前景广阔;Cu同位素在岩浆、热液、陆地系统可以很好地示踪氧化还原过程;Zn同位素由于络合过程分馏已经被用在许多不同环境中作为含硫/碳流体迁移的敏感示踪剂;Mo同位素作为古氧逸度计可有效重建古海洋-大气氧化还原状态。     

陆丰南地区断拗转换界面厘定及其地质意义

珠江口盆地经历裂陷阶段向拗陷阶段的转变，同期沉积地层记录了该构造变革和沉积演化过程，为厘定断拗转换界面提供了可能。基于地震反射、沉积旋回特征，识别出陆丰南地区恩平组内部存在全区可追踪对比的构造沉积转换面——T72界面，也是区分上下恩平组界面。对陆丰13洼洼间隆钻井LFA开展上下恩平组碎屑锆石U- Pb 定年、重矿物组分、元素分析，提出恩平组T72界面上下地层物源体系发生转变。结合区域沉积充填特征，表明陆丰南地区T72界面为断- 拗转换界面。具体表现为：下恩平组沉积期湖盆继承文昌期裂陷盆地特征，湖盆水体较深，物源主要为盆地内部的中生代基底凸起，沉积层序明显受盆内低凸起控制，在盆内低凸起四周发育一系列近源的辫状河三角洲，井区主要接受来自惠陆低凸起物源;上恩平组沉积期间，湖盆进入断拗过渡期，湖盆扩大、水体变浅，盆内低凸起四周的断裂活动减弱，沉积层序逐渐向盆内低凸起超覆，盆外太古宙—古生代物源组分供给不断加强，近源的三角洲砂体逐渐向远源的浅水三角洲砂体转化，同时发育宽广的滨浅湖环境，原供给物源的惠陆低凸起为水体淹没，井区接受了北部隆起外的物源。     

甘孜- 理塘洋可能存在北向俯冲：来自松潘- 甘孜道孚- 炉霍岩浆岩的证据

松潘- 甘孜造山带巨厚的三叠系复理石沉积盖层给探讨其基底性质、俯冲- 碰撞过程和深部岩浆作用增添了难度，使得带内广泛出露的花岗质岩体和少量镁铁质岩体成为解开松潘- 甘孜造山带构造演化谜团的重要研究对象。锆石U- Pb定年结果表明道孚花岗闪长岩形成于223. 5~217. 4 Ma，炉霍二长岩结晶年龄为219. 4 Ma，辉长岩为218. 9 Ma，均属于晚三叠世岩浆活动的产物。化学成分研究结果表明，花岗质岩石都表现出I型花岗岩特征，其中炉霍二长岩具有较高的Ba、Sr含量，相对较高且均一的εHf(t)值（-3. 69~-1. 65），表明其可能来源于富集玄武质新生下地壳的熔融。道孚花岗闪长岩具有分散的εHf(t)值（-13. 51~0. 41），野外和地球化学特征指示其形成于幔源熔体与古老壳源熔体的混合。辉长岩在微量元素蜘蛛图上具有类似的模式，不同程度富集Ba、Sr、Pb、Th和U元素，出现Nb、Ta、Ti元素亏损，具有岛弧玄武岩的特征，来源于流/熔体交代的地幔楔部分熔融。综合区域已有资料，我们对甘孜- 理塘洋的演化历史提出新的认识，认为甘孜- 理塘洋不仅仅存在向南俯冲的可能性，同时也具有北向俯冲的历史，晚三叠世道孚- 炉霍岩浆岩的形成受控于甘孜- 理塘洋向北边松潘- 甘孜地块俯冲的背景之下。     

Evaluating the mobility of137Cs,239+240Pu and210Pb from their distributions in laminated lake sediments

Post-depositional mobility of¹³⁷Cs,^239+240Pu and²¹⁰Pb was assessed in six small lake basins by comparing sedimentary nuclide profiles with their known fallout history. Laminae couplets, when present, were determined to be varves because the¹³⁷Cs and^239+240Pu 1963 fallout peaks are present in laminae couplets corresponding to years 1962–1964. There is no evidence of mobility of²¹⁰Pb, because 1) mass accumulation rates based on²¹⁰Pb agree with those based on¹³⁷Cs and^239+240Pu peak depths and with those based on varve counts, and 2)²¹⁰Pb ages agree with varve ages. Significant mobility of¹³⁷Cs is evident from the penetration of¹³⁷Cs to depths 15–20 cm deeper than^239+240Pu. Deep penetration of¹³⁷Cs in spite of a sharp gradient below the peak is interpreted by a numerical model to suggest that¹³⁷Cs is present in two distinct forms in these sediments, 67–82% as an immobile form and 18–33% reversibly adsorbed with a K _d of approximately 5000. The profiles can be interpreted equally well assuming a small portionof the total¹³⁷Cs was present as an extremely mobile phase (K _d 5000) in the months to years following peak fallout, slowly becoming more strongly adsorbed. High NH ₄ ⁺ concentrations in porewaters may enhance diffusion of the mobile form of¹³⁷Cs, but not of the immobile form of¹³⁷Cs that defines the sharp gradient. Mobility of¹³⁷Cs is likely also enhanced by the low clay content and the high porosity of these sediments. Thus the first detection of¹³⁷Cs in the sediments cannot automatically be assumed to correspond to a date of 1952 (initial testing of thermonuclear weapons), although the depth of the peak can be assumed to correspond to 1963 (the year of maximum fallout from testing of thermonuclear weapons).^239+240Pu is a more reliable sediment chronometer than¹³⁷Cs because it is significantly less mobile.This is the sixth of a series of papers to be published by this journal following the 20 ^th anniversary of the first application of²¹⁰Pb dating of lake sediments. Dr P.G. Appleby is guest editing this series.     

Low temperature volatile production at the Lost City Hydrothermal Field, evidence from a hydrogen stable isotope geothermometer

Although commonly utilized in continental geothermal work, the water-hydrogen and methane-hydrogen isotope geothermometers have been neglected in hydrothermal studies. Here we report δD-CH₄ and δD-H₂ values from high-temperature, black smoker-type hydrothermal vents and low-temperature carbonate-hosted samples from the recently discovered Lost City Hydrothermal Field. Methane deuterium content is uniform across the dataset at − 120 ± 12‰. Hydrogen δD values vary from − 420‰ to − 330‰ at high-temperature vents to − 700‰ to − 600‰ at Lost City. The application of several geothermometer equations to a suite of hydrothermal vent volatile samples reveals that predicted temperatures are similar to measured vent temperatures at high-temperature vents, and 20-60 °C higher than those measured at the Lost City vents. We conclude that the overestimation of temperature at Lost City reflects 1) that methane and hydrogen are produced by serpentinization at > 110 °C, and 2) that isotopic equilibrium at temperatures < 70 °C is mediated by microbial sulfate reduction. The successful application of hydrogen isotope geothermometers to low-temperature Lost City hydrothermal samples encourages its employment with low-temperature diffuse hydrothermal fluids.     

Thermal and isotopic profiling of the Pipeline hydrothermal system: Application to exploration for Carlin-type gold deposits

New exploration techniques are vital to the search for new orebodies in mature terranes, as well as for extensions of existing orebodies. This research focused on application of low-temperature dating techniques (primarily apatite fission-tracks) and stable isotope measurements (carbon and oxygen in carbonate rocks) in and around the Pipeline deposit, a Carlin-type gold system. The primary purpose of the project was to assess whether these techniques could provide exploration vectors that might be used in conjunction with other geologic, geochemical, and geophysical techniques to determine the locus of fossil hydrothermal fluid flow, and the attendant possibility of finding economic mineral deposits.At Pipeline, measurements of apatite fission-tracks and (U − Th) / He geochronometry yield a clear indication of the elevated temperatures associated with the fossil hydrothermal system. The pattern is one of a central target (Pipeline deposit) with decreasing thermal effects as far as several kilometers laterally from the known ore zone. Because of the irregular nature of fluid flow through fractures, a significant number of samples are required to discern this pattern, but the pattern is quite clear from the 32 samples in and around the Pipeline pit.Stable isotope measurements of carbonate rocks yield patterns centered on the Pipeline pit area. Oxygen isotopes in particular are shifted toward lower values as the result of interaction between the hydrothermal fluids and carbonate rocks. Carbon isotopes show a pattern, but it is somewhat more difficult to interpret than the oxygen isotope pattern. As with the geochronometric patterns, isotopic indications of fluid flow are present several kilometers from the ore zone at Pipeline. Also as with the geochronometric data, a relatively large sample set is required to see the pattern. At Pipeline, the patterns are evident in approximately 45 surface samples and very clearly in the cross-sections containing approximately 100 samples.From these data, it is clear that thermal and stable isotopic measurements on rocks at a significant distance from the known Pipeline hydrothermal system record the passage of hot fluids through the rock. Both techniques provide a footprint of the Pipeline system that is several diameters larger than the ore zone (as presently known). Therefore, thermochronologic and stable isotopic measurements can be utilized in conjunction with other techniques as part of an overall exploration strategy for Carlin-type deposits. Although these techniques do not provide a direct indication of the metal content of the fossil hydrothermal fluids, they do provide an indication of the robustness of fluid flow and the potential size of a hydrothermal system.     

Are the South and North Liaohe Groups of North China Craton different exotic terranes? Nd isotope constraints

The Liaohe Group is an important Paleoproterozoic stratigraphic unit in the northeastern part of the North China Craton and is traditionally subdivided into the North and South Liaohe Groups. Associated with both the North and South Liaohe Groups are voluminous Paleoproterozoic granitoid rocks, named the Liaoji granitoids. Different tectonic models, including terrane amalgamation, continent–arc collision and rift closure, have been proposed to interpret the tectonic setting and evolution of the North and South Liaohe Groups and associated Liaoji granitoids. At the centre of the controversy between these models is whether or not the North and South Liaohe Groups developed on the same Archean basement. Nd isotopic geochemistry of the Liaoji granitoids provides important constraints on this controversial issue. The Liaoji granitoids associated with the North and South Liaohe Groups display similar ε_Nd values, restricted to a narrow range from 0 to 2, implying that these granitoid rocks were derived from the same or a similar magma source. Moreover, the Liaoji granitoids associated with the North and South Liaohe Groups have similar Nd model ages (T_DM), ranging from 2.4 to 2.6 Ga, suggesting that the protoliths of the Liaoji granitoids associated with both groups may have formed simultaneously, and that the basement rocks underneath the Liaoji granitoids and associated North and South Liaohe Groups belong to the same continental block rather than two different blocks. Combining lithological, structural and geochronological considerations, we interpret the North and South Liaohe Groups as having developed on a single late Archean basement that underwent Paleoproterozoic rifting associated with the intrusion of the Liaoji granitoids and the formation of the Liaohe Group, and closed upon itself in the Paleoproterozoic.     

The timing of ultrahigh-temperature metamorphism in Southern India: U–Th–Pb electron microprobe ages from zircon and monazite in sapphirine-bearing granulites

We report here U–Pb electron microprobe ages from zircon and monazite associated with corundum- and sapphirine-bearing granulite facies rocks of Lachmanapatti, Sengal, Sakkarakkottai and Mettanganam in the Palghat–Cauvery shear zone system and Ganguvarpatti in the northern Madurai Block of southern India. Mineral assemblages and petrologic characteristics of granulite facies assemblages in all these localities indicate extreme crustal metamorphism under ultrahigh-temperature (UHT) conditions. Zircon cores from Lachmanapatti range from 3200 to 2300 Ma with a peak at 2420 Ma, while those from Mettanganam show 2300 Ma peak. Younger zircons with peak ages of 2100 and 830 Ma are displayed by the UHT granulites of Sengal and Ganguvarpatti, although detrital grains with 2000 Ma ages are also present. The Late Archaean-aged cores are mantled by variable rims of Palaeo- to Mesoproterozoic ages in most cases. Zircon cores from Ganguvarpatti range from 2279 to 749 Ma and are interpreted to reflect multiple age sources. The oldest cores are surrounded by Palaeoproterozoic and Mesoproterozoic rims, and finally mantled by Neoproterozoic overgrowths. In contrast, monazites from these localities define peak ages of between 550 and 520 Ma, with an exception of a peak at 590 Ma for the Lachmanapatti rocks. The outermost rims of monazite grains show spot ages in the range of 510–450 Ma.While the zircon populations in these rocks suggest multiple sources of Archaean and Palaeoproterozoic age, the monazite data are interpreted to date the timing of ultrahigh-temperature metamorphism in southern India as latest Neoproterozoic to Cambrian in both the Palghat–Cauvery shear zone system and the northern Madurai Block. The data illustrate the extent of Neoproterozoic/Cambrian metamorphism as India joined the Gondwana amalgam at the dawn of the Cambrian.