西藏波龙斑岩铜金矿床钾长石和绢云母40Ar/39Ar年龄及其地质意义

西藏波龙斑岩铜金矿床是新近在青藏高原中部发现的规模最大的斑岩型矿床。文章对该矿床内的蚀变钾长石和蚀变绢云母进行了⁴⁰Ar/³⁹Ar年代学测试,获得蚀变钾长石的⁴⁰Ar/³⁹Ar坪年龄为(118.33±0.60) Ma,反等时线年龄为(118.49±0.74) Ma (初始⁴⁰Ar/³⁶Ar=286.1±8.4),表明波龙斑岩铜金矿床的钾化蚀变年龄为118~119 Ma;蚀变绢云母的⁴⁰Ar/³⁹Ar坪年龄为(121.61±0.67) Ma,反等时线年龄为(121.1±2.0) Ma (初始⁴⁰Ar/³⁶Ar=279±19)。由于蚀变绢云母测试样品内可能混入了斜长石,受其影响,蚀变绢云母测年结果的下限可能代表了该矿床绢英岩化蚀变年龄。这些蚀变钾长石和蚀变绢云母⁴⁰Ar/³⁹Ar测年结果与波龙矿床的成岩年龄值和成矿年龄值在误差范围内基本一致,表明该矿床的钾化和绢英岩化与成岩、成矿同期,该矿床的岩浆-热液活动过程的时限为121~118 Ma。     

柴北缘锡铁山榴辉岩退变质成因角闪石40Ar/39Ar年代学研究

采用激光阶段加热⁴⁰Ar/³⁹Ar技术,对柴达木盆地北缘锡铁山榴辉岩退变质作用形成的榴闪岩和斜长角闪岩之角闪石进行了定年分析。09NQ44Amp来自榴闪岩,各阶段表观年龄(以现代空气氩⁴⁰Ar/³⁶Ar比值295.5扣除非放射性成因⁴⁰Ar)构成了单调下降的阶梯状年龄谱。在反等时线图解上,2~4阶段数据点和5~18阶段数据点分别构成了两条等时线,等时年龄分别为427.6±10Ma和425.1±2.6Ma,对应的初始⁴⁰Ar/³⁶Ar比值则分别为435.2±6.1和705.3±13。角闪石09NQ43Amp来自榴辉岩强烈退变质作用形成的斜长角闪岩,⁴⁰Ar/³⁹Ar阶段加热分析也获得单调下降的年龄谱,在反等时线图解上其数据点3~6阶段和7~16阶段分别构成了两条等时线,等时年龄分别为418.9±2.9Ma和418.1±2.1Ma,对应的初始⁴⁰Ar/³⁶Ar比值则分别为493.7±2.8和685.8±34.3。等时线截距值高于现代大气⁴⁰Ar/³⁶Ar比值,表明角闪石中含过剩⁴⁰Ar。同时,由低温和中-高温阶段加热数据点分别构成两条等时年龄基本一致,截距值却明显不同的等时线,表明在角闪石热力学性质不同的源区,存在两期明显不同且未混合的初始捕获Ar组分。等时年龄425~418Ma代表的是锡铁山榴辉岩角闪岩相退变质作用发生的时间。等时线图解法虽然有效的校正了角闪石中的过剩⁴⁰Ar,但仅根据表观年龄图谱和等时线图谱还无法清晰判断过剩⁴⁰Ar在角闪石中的赋存状态,有待进一步探讨。     

泥炭样品的AMS 14 C年龄测定: 全样、植物残体和孢粉浓缩物*

沉积物¹⁴ C的年龄测定一直是第四纪年代学研究的热点。文章对中国干旱、半干旱地区的内蒙古库伦泥炭剖面的泥炭全样、植物残体和孢粉浓缩物进行了AMS ¹⁴ C测年比较研究。从泥炭沉积物中提取用于AMS ¹⁴ C测年的孢粉浓缩物的关键步骤包括:过筛(125μm,63μm和10μm),重液浮选(比重1.9)及在180倍的体视显微镜下进行手工挑选。测年结果表明:孢粉浓缩物的测年值比同一层位的泥炭沉积物全样或植物残体的测年值老225~340年; 植物残体与孢粉浓缩物的测年结果较为接近。但是,距地表24~27cm处孢粉浓缩物给出了610~780A.D.的年龄值,远老于其下样点的年龄,而泥炭全样为现代样品,二者相差1255年,这可能与该样品孢粉纯度较低、掺杂有一些老碳物质燃烧后形成的微粒杂质有关。因此,提高孢粉纯度对孢粉浓缩物¹⁴ C测年至关重要。     

青藏高原若干地点的第四纪冰川年代学* ——深切怀念孙殿卿院士

青藏高原第四纪冰川时空演化问题广受关注。应用宇宙成因核素暴露年龄测定方法开展高原古冰川的年代学研究,对青藏高原聂拉木、唐古拉山、义敦海子山和折多山等4个地区的第四纪冰碛物进行了\{¹⁰ Be\},²⁶ Al和²¹ Ne暴露年龄测定,获得了青藏高原不同地点第四纪冰川发育的年代学数据,结果表明青藏高原出现了多期第四纪冰期,分别为YD事件、末次冰期晚阶段、末次冰期早阶段、倒数第2次冰期和倒数第3次冰期。     

深海沉积物10Be记录研究

DSDP519钻孔¹⁰Be测定结果表明，在B／M，M／G两地磁极性倒转期间，¹⁰Be产生率均约增加20％。DSDP519孔δ¹⁰Be曲线与DSDP502孔δ¹⁸O曲线具有明显的正相关关系。CT85－5钻孔¹⁰Be曲线在34000±3000aB．P存在明显的峰，峰值比正常值高出2．5倍，⁹Be，Zn变化曲线中均未观察到此峰，与Vostok冰芯¹⁰Be峰在时间上属于同期。这进一步说明了此时期内¹⁰Be浓度增加是全球性的，只能归因于¹⁰Be产生率的增加。Raisbeck峰讯号可以成为某些储存库精确时标。     

东喜马拉雅构造结气候构造作用下热史演化的40Ar/39Ar年代学记录

以喜马拉雅山系为典型实例,究竟是气候作用还是构造作用引起山体隆升的问题已经成为地球系统科学研究中的重要前沿问题。无论是气候因素还是构造因素引起山体隆升,二者都与一个共同的地表过程——剥蚀作用相关,剥蚀作用对山体中地质体的影响可以用岩石矿物经历的热史演化来描述,所以,在造山作用研究中,山体或山脉的热史演化是揭开地质体经历地质过程、山体隆升研究的重要途径。利用河砂组成矿物来研究流域的地质过程和构造演化已经成为现代地质科学的重要手段。本文采集了雅鲁藏布江下游墨脱县以南约50 km处地东河段内的现代河砂,对其中的角闪石、白云母、黑云母及钾长石等四种矿物进行了高精度单颗粒激光⁴⁰Ar/³⁹Ar年代学测试,并进行了概率统计。地东河段河砂中富钾矿物⁴⁰Ar/³⁹Ar年代学统计结果显示,大峡谷流域的热史演化可以确定有多个阶段,分别可以识别出70~69、61~60、43~42、35~34、26~25、25~23、22~20、20~18、17~14、12~11、8~6、5~4及<2Ma等13个热史演化阶段。通过将上述热史信息与印度大陆与欧亚大陆碰撞角度和碰撞速率变化曲线的对比,可以确定70~69、61~60、43~42、35~34、22~20和12~11Ma等6个阶段的年代学信息是两大陆碰撞角度和碰撞速率变化事件在东喜马拉雅构造结热史上的记录;通过与全球深海氧、碳同位素记录曲线的对比,可以认为26~25、25~23、17~14、8~6、5~4和<2Ma等6个阶段的年代学信息是气候变化在东喜马拉雅构造结热史上的记录。东喜马拉雅构造结地质体热史演化是构造与气候相互作用的结果。     

现代沉积的210Pb计年

²¹⁰Pb具有百年时间尺度沉积计年的重要价值。²¹⁰Pb_ex计年假设：沉积物是封闭系统；进入水体的²¹⁰Pb能有效地转移到沉积物中并不发生沉积后迁移；非过剩²¹⁰Pb与其母体²²⁶Ra保持平衡。²¹⁰Pb_ex计年可用稳定输入通量-稳定沉积物堆积速率模式、常量初始浓度模式或恒定补给速率模式。沉积物柱芯必须保持原态并以0．5～1cm间隔分截；用相应层节²²⁶Ra校正。沉积物表层混合作用及²²²Rn的丢失可能导致顶部²¹⁰Pb_ex异常。季节性缺氧湖泊沉积物顶部可能存在²¹⁰Pb及²¹⁰Po的再迁移。²¹⁰Pb与¹³⁷Cs两种计年方法原理上具有根本差别。²¹⁰Pb，¹³⁷Cs与沉积纹理方法对比是准确计年的重要保证。     

现代沉积年分辨的137Cs计年──以云南洱海和贵州红枫湖为例

1964,1975及1986年三个¹³⁷CS时标计算出红枫湖和洱海沉积物平均堆积速率完全一致,说明1975年和1986年次级蓄积峰作为计年时标的可靠性。洱海沉积物平均堆积速率为0．047±0．002g／(cm²·a),与²¹⁰Pb方法所获得的结果一致;红枫湖为0．17±0．01g／(cm²·a),与其建湖以来沉积物实际堆积的观察结果吻合。洱海1964年沉积物中¹³⁷CS的比活度(校正到沉积年代)仅46．4Bq／kg,而红枫湖达145Bq／kg。由于红枫湖沉积物堆积速率约为洱海的3．7倍,所以其1964年层节沉积物中¹³⁷CS蓄积量比洱海大11.5倍。红枫湖沉积物中¹³⁷CS累计值的99．4％分配于1985年以前,而洱海的19．4％分配于1986年以后,显示出¹³⁷CS在洱海沉积物中的较大扩散能力。     

东平湖沉积物 210Pb、137Cs 垂直分布及年代学意义

对东平湖沉积物柱状岩芯放射性年代学研究表明： 12cm处的 ¹³⁷Cs比活度峰值对应于1963年人工核试验高峰,9cm和6cm处的 ¹³⁷Cs比活度蓄积峰可能分别与1974年的全球核素散落和1986年前苏联切尔诺贝利核电站核泄漏有关; ²¹⁰Pb比活度随深度呈指数衰减,利用 ¹³⁷Cs核素1963年对应的蓄积峰进行校正,采用 ²¹⁰Pb计年的CRS模式建立了1889年以来东平湖现代沉积年代序列。根据 ²¹⁰Pb年代序列,计算了东平湖现代沉积速率,发现近百年来东平湖地区沉积速率有明显变化： 1889～1945年,沉积速率较高,平均达0.297g/cm2•a; 1945～1963年,沉积速率整体处于下降趋势; 1963～2000年,沉积速率比较稳定,平均约0.141g/cm2•a; 约2000年以来,沉积速率有增高趋势。通过分析认为,1945年以前东平湖较高的沉积速率可能与东平湖作为黄河水的自然滞洪区有关; 1950年代国家对东平湖的治理改造,控制了黄河水的自然倒灌,导致了东平湖沉积速率的迅速下降; 1963年以后,由于黄河上中游大型水利工程设施的修建,抑制了东平湖调洪功能的发挥,导致东平湖沉积速率低而稳定; 近年来,东平湖沉积速率有增大趋势,这可能与湖区人民发展围网养殖带入较多的沉积物有关。     

西藏东南部察隅地区德玛拉岩群的同位素年代学研究及其意义

青藏高原冈底斯地块东南部的德玛拉岩群为一套角闪岩相变质岩系,一直被认为是前寒武纪变质基底,但并没有可靠的年代学证据。论文对采自其中的黑云角闪片岩和黑云母石英片岩进行了锆石LA-ICP-MS U-Pb定年和黑云母³⁹Ar-⁴⁰Ar定年,测试表明,黑云角闪片岩原岩锆石U-Pb年龄为217.1Ma,由黑云母³⁹Ar-⁴⁰Ar获得的变质年龄为22.3Ma,黑云母石英片岩中碎屑锆石主要为岩浆成因,年龄范围主要集中在520~600Ma和900~1100Ma,黑云母³⁹Ar-⁴⁰Ar变质年龄为16.3Ma和22.3Ma。上述结果虽不能完全否定西藏东南部察隅地区前寒武纪基底变质岩系的存在,但至少说明现今的德玛拉岩群中还包含有遭受中生代岩浆侵入的古生代沉积岩,它们在新生代经历了变质和岩浆作用的再造,是一套变质杂岩。     

A chlorine-36 study of regional groundwater flow and vertical transport in southern Nevada

Chlorine-36 data for groundwater from the Death Valley regional flow system is interpreted in the context of existing conceptual models for regional groundwater flow in southern Nevada. Chlorine-36 end member compositions are defined for both recharge and chemically evolved groundwater components. The geochemical evolution of ³⁶Cl is strongly controlled by water-rock interaction with Paleozoic carbonate rocks that comprise the regional aquifer system, resulting in chemically evolved groundwater that is characteristically low in ³⁶Cl/Cl and high in Cl. Groundwater from alluvial and volcanic aquifers that overlie the regional carbonate aquifer are generally characterized by high ³⁶Cl/Cl and low Cl signatures, and are chemically distinct from water in the regional carbonate aquifer. This difference provides a means of examining vertical transport and groundwater mixing processes. In combination with other geochemical and hydrogeologic data, the end members defined here provide constraints on aquifer residence times and mixing ratios.     

Chlorine-36 and the initial value problem

 Chlorine-36 is a radionuclide with a half-life of 3.01×10⁵a. Most ³⁶Cl in the hydrosphere originates from cosmic radiation interacting with atmospheric gases. Large amounts were also produced by testing thermonuclear devices during 1952–58. Because the monovalent anion, chloride, is the most common form of chlorine found in the hydrosphere and because it is extremely mobile in aqueous systems, analyses of both total Cl^– as well as ³⁶Cl have been important in numerous hydrologic studies. In almost all applications of ³⁶Cl, a knowledge of the initial, or pre-anthropogenic, levels of ³⁶Cl is useful, as well as essential in some cases. Standard approaches to the determination of initial values have been to: (a) calculate the theoretical cosmogenic production and fallout, which varies according to latitude; (b) measure ³⁶Cl in present-day precipitation and assume that anthropogenic components can be neglected; (c) assume that shallow groundwater retains a record of the initial concentration; (d) extract ³⁶Cl from vertical depth profiles in desert soils; (e) recover ³⁶Cl from cores of glacial ice; and (f) calculate subsurface production of ³⁶Cl for water that has been isolated from the atmosphere for more than one million years. The initial value from soil profiles and ice cores is taken as the value that occurs directly below the depth of the easily defined bomb peak. All six methods have serious weaknesses. Complicating factors include ³⁶Cl concentrations not related to cosmogenic sources, changes in cosmogenic production with time, mixed sources of chloride in groundwater, melting and refreezing of water in glaciers, and seasonal groundwater recharge that does not contain average year-long concentrations of ³⁶Cl. Received, December 1996 · Revised, August 1997 · Accepted, August 1997     

Dating of syngenetic ice wedges in permafrost with 36Cl

A new method of permafrost dating with the cosmogenic radionuclide ³⁶Cl is presented. In the first application, syngenetic ice wedges are dated using the ratio of ³⁶Cl and Cl concentrations in ice as the signal. ³⁶Cl is produced in the atmosphere by nuclear reactions of cosmic rays on argon. Stable chlorine enters the atmosphere from the oceans. Their ratio does not depend on chloride concentration in precipitations and on sublimation of snow. In situ production of ³⁶Cl in permafrost ice via cosmic ray-induced reactions and neutron capture are calculated and the dating age limit is estimated as 3 million years. ³⁶Cl/Cl ratios in permafrost samples from cape Svyatoy Nos (Laptev Sea coast), North-Eastern Siberia, are measured by accelerator mass spectrometry. Analysis of the first results and the calculated dates support the feasibility of the ³⁶Cl permafrost dating method     

琼北火山岩激光40Ar/39Ar定年研究

新生代以来,雷琼地区多次、大量地喷发了一系列火山岩。前人主要基于K-Ar法对此划分了期次。本文采用激光40Ar/39Ar年代学方法,对琼北火山岩区进行了精细定年研究。低本底激光40Ar/39Ar法能够对低钾含量,极少量样品(毫克级)进行精细测定,非常适合极年轻火山岩的定年工作。结果显示的火山岩激光40Ar/39Ar法高质量数据表明琼北火山喷发活动时限跨越1.3～0.052Ma。在比较了表观年龄与等时线年龄差异之后,本文给出了年龄推荐值。正如测试数据所显示,本地区新生代火山岩普遍存在40Ar和36Ar过剩的问题,此时只有等时线年龄才代表喷发的真实年龄。     

The last glaciation of the Arctic volcanic island Jan Mayen

The volcanic island of Jan Mayen, remotely located in the Norwegian-Greenland Sea, was covered by a contiguous ice cap during the Late Weichselian. Until now, it has been disputed whether parts of the island south of the presently glaciated Mount Beerenberg area were ever glaciated. Based on extensive field mapping we demonstrate that an ice cap covered all land areas and likely also extended onto the shallow shelf areas southeast and east of the island. Chronological interpretations are based on K-Ar and ⁴⁰Ar/³⁹Ar dating of volcanic rocks, cosmogenic nuclide (³⁶Cl) surface exposure dating of bedrock and glacial erratics, and radiocarbon dating. We argue that ice growth started after 34 ka and that an initial deglaciation started some 21.5–19.5 ka in the southern and middle parts of the island. In the northern parts, closer to the present glaciers, the deglaciation might have started later, as evidenced by the establishment of vegetation 17–16 cal. ka BP. During full glaciation, the ice cap was likely thickest over the southern part of the island. This may explain a seemingly delayed deglaciation compared with the northern parts despite earlier initial deglaciation. In a broader context, the new knowledge of the Late Weichselian of the island contributes to the understanding of glaciations surrounding the North Atlantic and its climate history.     

Stable chlorine isotopes in arid non-marine basins: Instances and possible fractionation mechanisms

Stable chlorine isotopes are useful geochemical tracers in processes involving the formation and evolution of evaporitic halite. Halite and dissolved chloride in groundwater that has interacted with halite in arid non-marine basins has a δ³⁷Cl range of 0 ± 3‰, far greater than the range for marine evaporites. Basins characterized by high positive (+1 to +3‰), near-0‰, and negative (−0.3 to −2.6‰) are documented. Halite in weathered crusts of sedimentary rocks has δ³⁷Cl values as high as +5.6‰. Salt-excluding halophyte plants excrete salt with a δ³⁷Cl range of −2.1 to −0.8‰. Differentiated rock chloride sources exist, e.g. in granitoid micas, but cannot provide sufficient chloride to account for the observed data. Single-pass application of known fractionating mechanisms, equilibrium salt-crystal interaction and disequilibrium diffusive transport, cannot account for the large ranges of δ³⁷Cl. Cumulative fractionation as a result of multiple wetting-drying cycles in vadose playas that produce halite crusts can produce observed positive δ³⁷Cl values in hundreds to thousands of cycles. Diffusive isotope fractionation as a result of multiple wetting-drying cycles operating at a spatial scale of 1–10 cm can produce high δ³⁷Cl values in residual halite. Chloride in rainwater is subject to complex fractionation, but develops negative δ³⁷Cl values in certain situations; such may explain halite deposits with bulk negative δ³⁷Cl values. Future field studies will benefit from a better understanding of hydrology and rainwater chemistry, and systematic collection of data for both Cl and Br.     

Characteristics of deep groundwater flow in a basin marginal setting at Sellafield,Northwest England: Cl and halide evidence

A number of chemical and physical processes inside and outside a sedimentary basin (e.g. evaporite dissolution and topographic drive, respectively) affect groundwater flow near the basin’s margin. Contrasting formations at the margin, typically basinal sedimentary rocks and basement, are host to the interplay between these processes so that groundwater flows and compositions change within a relatively small volume. To interpret how groundwater flow and geochemistry have evolved, interactions between these processes must be understood. Such interactions were investigated near the margin of the East Irish Sea Basin in NW England, by sampling deep groundwaters (to 1500 m below sea level) from Ordovician volcanic basement rocks and Carboniferous to Triassic sedimentary cover rocks. Variable Br/Cl ratios and Cl concentrations in deep saline waters and brines indicate mixing patterns. Variations in ³⁶Cl/Cl constrain the timing of mixing. Relatively low Br/Cl ratios (ca. 1 × 10⁻³ by mass) characterise brine from the western sedimentary cover and reflect halite dissolution further west. Saline water with relatively high Br/Cl ratios (ca. 2 × 10⁻³ by mass) of uncertain origin occupies the eastern basement. These two waters mix across the area. However, mixing alone cannot explain variable ³⁶Cl/Cl ratios, which partly reflect differing in situ³⁶Cl production rates in different rock formations. Most ³⁶Cl/Cl ratios in groundwater sampled from the eastern metavolcanic basement (mean = 25 × 10⁻¹⁵) and western sedimentary cover (mean = 10 × 10⁻¹⁵) are at or close to equilibrium with in situ³⁶Cl production. These variations in ³⁶Cl/Cl across the site possibly took >1.5 Ma to be attained, implying that deep groundwater flow responded only slowly to the Quaternary glaciation of the site. Interplay between varied processes in basin marginal settings does not necessarily imply flow instability.     

Abundances of F,Cl S and P in Volcanic Magmas and Their Evolution,Wudalianchi

F, Cl, S and P were determined, using electron microprobe, in magmatic inclusions trapped within minerals and glass mesostasis from Wudalianchi volcanic rocks. The initial volcanic magma from Wudalianchi corresponds to the basanitic magma crystallized near the surface ( pressure < 91 Mpa ). The potential H₂O content of this magma is in the range 2 — 4 wt. %. The initial composition of volcanic magmas varies regularly from early to late volcanic events. From the Middle Pleistocene to the recent eruptions (1719 – 1721 yr.), the basicity of volcanic magma tends to increase, as reflected by an increase in MgO and CaO contents and by a progressive decrease in SiO₂ and K₂O contents. Meanwhile. from early (Q₂ ) to late (Q₃) episodic eruptions of the Middle Pleistocene, the initial concentrations of chlorine in volcanic magmas range from 1430 – 1930 ppm to 1700 ppm and decrease to 700 — 970 ppm for the first episodic eruption during the Holocene (Q ₄ ¹ ). The chlorine concentrations of volcanic magmas of recent eruption (Q ₄ ² ) are increased again to 2600 – 2870 ppm. A parallel evolution trend for phosphorus and chlorine concentrations in magmas has been certified: 1500 – 5970 ppm (Q₂)→ 3500 – 4210 ppm (Q₃)→ 1100– 3500 ppm (Q ₄ ¹ )→ 6800– 7900 ppm (Q ₄ ² ). The fluorine contents of volcanic magmas, from early to late volcanic events, show the same trend: 770 – 2470 ppm → 200–700 ppm → 700 – 800 ppm. During the crystallization-evolution of volcanic magmas, fluorine and phosphorus tend to be enriched in residual magmas as a result of crystal-melt differentiation. for example. the fluorine contents reach 5000– 6800 ppm and the phosphorus contents, 2.93wt.% in residual magmas. An appreciable amount of chlorine may be lost from water rich volcanic magmas prior to eruption as a result of degassing. Apparently, water serves as a gas carrier for the chlorine. The chlorine contents of residual magmas may decrease to 100 – 300 ppm. The volcanic magmas from Wudalianchi are poor in sulfur, normally ranging from 200 to 400ppm. On account of the behavior of sulfur in magmas and the strontium and oxygen isotopic analyses ((⁸⁷Sr /⁸⁶Sr)_i=0.70503– 0.70589; δ¹⁸O = + 5.50 – + 6.89 ‰ ), it can be considered that the basanitic magmas in the Wudalianchi volcanic area came from the upper mantle and have not yet been contaminated probably by continental crust materials.     

Control of Cl production in carbonaceous shales by phosphate minerals

When using ³⁶Cl to date very old groundwater in regional aquifer systems, knowledge of the subsurface ³⁶Cl input into the aquifer system is essential. Although ³⁶Cl can be produced through nuclear reactions in the subsurface, in many situations, the input of ³⁶Cl into sedimentary aquifer systems by this avenue of production can be neglected. This is a valid assumption when investigating long-flowpath groundwater systems composed of sandstones, limestones, and shales of typical composition. These rock types are not sufficiently enriched in radioactive elements to produce significant ³⁶Cl in the deep subsurface. Carbonaceous shales, on the other hand, can concentrate the radioactive elements necessary to produce significant ³⁶Cl in the deep subsurface. Chlorine-36 ratios (³⁶Cl/Cl) for a suite of Late Devonian and Pennsylvanian carbonaceous shales were calculated from bulk-rock chemistry as well as measured using accelerator mass spectrometry. The poor agreement between calculated and measured ratios is the result of the assumption of chemical homogeneity used by the calculation algorithm, an assumption that was not satisfied by the carbonaceous shales. In these shales, organic matter, clay minerals, and accessory minerals are heterogeneously distributed and are physically distinct on a micron-order scale. Although organic matter and clay minerals constitute the overwhelming bulk of the shales, it is the phosphate minerals that are most important in enhancing, and suppressing, ³⁶Cl production. Minerals such as apatite and carbonate-apatite (francolite)—by including uranium, rare earth elements (REEs), and halogens—have an important impact on both neutron production and thermal neutron absorption. By incorporating both uranium and fluorine, phosphate minerals act as neutron production centers in the shale, increasing the probability of ³⁶Cl production. By incorporating REEs and chlorine, phosphate minerals also act to shield ³⁵Cl from the thermal neutron flux, effectively suppressing the production of ³⁶Cl. To reconcile the measured ³⁶Cl ratios with the ratios calculated assuming chemical homogeneity, the shales were artificially split into three fractions: organic, clay mineral, and phosphate mineral. Neutron production was calculated separately for each fraction, and the calculation results demonstrated that the phosphate fraction exerted much more control on the ³⁶Cl ratio than the organic or clay mineral fractions. By varying the uranium and chlorine contents in the phosphate fraction, a new, heterogeneous ³⁶Cl ratio was calculated that agreed with the measured ratio for the overwhelming majority of the carbonaceous shales. When using rock chemistry to calculate the ³⁶Cl ratio, rock types that show mineralogical heterogeneity on a micron scale can be divided into bulk fractions and accessory fractions for separate calculations of neutron production and neutron absorption. In this manner, a more accurate, heterogeneous ³⁶Cl ratio can be calculated for the rock as a whole.     

(极)年轻火山岩激光熔蚀40Ar/39Ar定年

对中国大量年轻或/和极年轻火山岩的定年实践研究表明,(极)年轻火山岩的激光熔蚀40Ar/39 Ar定年具有不同于第四纪以前喷发火山岩定年的显著特点.激光熔蚀40Ar/39Ar定年技术因为本底低、样品用量小以及与现代惰性气体同位素质谱设备在灵敏度、高精度方面的相一致,在年轻火山岩的定年中得到深入运用.借助激光在年轻或/和极年轻火山岩的40 Ar/39 Ar定年中,实践证明,样品形成时限越年轻(特别是相当于第四纪时期的样品),Nier值与样品中初始氩比值的偏离会引起K-Ar和40Ar/39 Ar表观年龄的偏差越大.对于小于0.2Ma的样品,Nier值与样品中初始氩比值的偏离对K-Ar和40Ar/39Ar表观年龄的偏差影响呈指数增长;当样品年龄相对较老(老于第四纪)时,Nier值和初始氩比值的偏离对K-Ar和40Ar/39 Ar表观年龄的影响较小.以40Ar/ArAr定年为出发点,定量给出界定年轻与极年轻火山岩的年龄:2～0.2Ma的火山岩界定为年轻火山岩,0.2Ma以来的火山岩称为极年轻火山岩.实验结果还证实,测定(极)年轻火山岩基质年龄时要尽量剔除非同源分馏的斑晶,以便去除斑晶可能带来的过剩氩影响;年轻火山岩样品的测年,应根据岩石结构和粒度特征选取合适的粒度,通常情况下,推荐0.2mm颗粒直径(60～80目)为理想粒径;年轻火山岩样品在快中子辐照后冷却放置时间不宜过长,否则造成37 Ar测不准,影响数据结果,带来较大偏差;激光40Ar/39Ar精细定年对标准样品的均一性有很高的要求,通过标定常用的国内外监测标样发现,标样SB-778-Bi,Bem4M,BT-1均一性很好,适合用作激光熔蚀40Ar/39Ar定年监测;测试数据的处理中,火山岩喷发后冷却结晶中同时形成的斑晶和基质的等时线处理能够帮助获得客观真实和精细的年龄结果.在此基础上,北京大学惰性气体同位素实验室建成了专用于(极)年轻火山岩精细定年的激光熔蚀40Ar/39Ar定年实验流程.