Carbon isotopes, time boundaries and evolution

The carbon isotope composition of carbonate rocks in time-boundary zones is interpreted as a reflection of the variations in the total biomass at mass extinction events. Better stratigraphic control and identification of hiatuses can be gained by stable isotope stratigraphic methods than with any other type of stratigraphy. It is suggested that the use of carbon isotopes can help in solving some of the problems confronting palaeontologists and lead to a better understanding of the evolutionary significance of these events.     

Radium isotopes in saline seepages,south-western Yilgarn,Western Australia

Water samples from saline seepages in the south-western Yilgarn Block of Western Australia contain high activities of the four naturally-occurring radium isotopes. Activities of up to 310 $\text{pCi}\text{l}$ for ²²⁶Ra and 1720 $\text{pCi}\text{l}$ for ²²⁸Ra were measured and the ${}^{228}\text{Ra}{}^{226}\text{Ra}$ ratio averaged 6.1. Activities of the two short-lived radium isotopes were also high. ²²³Ra activities of up to 94 $\text{pCi}\text{l}$ were found with an average ${}^{226}\text{Ra}{}^{223}\text{Ra}$ ratio of 3.3, considerably lower than the natural abundance ratio of 21.4. Activities of up to 23 $\text{pCi}\text{l}$²²⁷Ac, the long-lived ($\text{t}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 22 years}$) grandparent of ²²³Ra, were also measured. The analysis of surface granite samples, the probable source rocks of the radium, gave $\text{Th}\text{U}$ activity ratios of around 1.5. The higher ${}^{228}\text{Ra}{}^{226}\text{Ra}$ ratios of the waters were attributed to readily leached ²²⁸Ra in the weathered granites as a result of thorium remaining after weathering. Leach experiments on U-Th ore by NaCl solutions showed that all four radium isotopes were equally leached. Sulphate anions reduced the ²²⁶Ra and ²²⁸Ra leaching to a greater extent than for ²²³Ra and ²²⁴Ra, suggesting that the latter isotopes were being supported in solution by parent isotopes. In particular this suggested ²²⁷Ac was leached into the sulphate solution but this does not fully account for the amount of ²²⁷Ac seen in the seepage waters.     

黔南坳陷油苗来源:碳、硫同位素及生物标志物证据

为明确黔南坳陷不同层位油苗来源,在广泛采集不同层位烃源岩、油苗样品的基础上,采用GC、GC-MS及GC-IRMS等方法对其碳、硫同位素及生物标志物特征进行系统分析,进而开展了油源对比.结果表明:油苗的δ13C值为-33.04‰～-31.63‰,平均-32.26‰(n=18);δ34S值为+16.06‰～+23.06‰,平均+18.99‰(n=4);油苗遭受不同程度生物降解,常规甾、萜烷面貌特征差异较大,但普遍含有较丰富的三环萜烷、伽玛蜡烷、三芳甾烷、芳基类异戊二烯烃、惹烯和硫芴;C25三环萜烷/C24四环萜烷值、二苯并噻吩/菲与Pr/Ph相关图表明油苗为典型海相原油;Ts/(Ts +Tm)、C29甾烷20S/(20S+ 20R)及甲基菲指数等均表明油苗为成熟-高熟原油.研究区下寒武统牛蹄塘组黑色泥岩干酪根δ13C值为-35.79‰～-29.88‰,平均-32.85‰(n=35),与油苗相关性良好,而泥盆系、石炭系和二叠系烃源岩δ13C值显著偏重,均大于-29‰;下寒武统牛蹄塘组黑色泥岩干酪根δ34S值为+ 14.78‰～+ 17.60‰,平均+16.32‰(n=4),与油苗具有很好的可比性,而下、中泥盆统黑色泥岩干酪根δ34S值分别为-9.10‰～-6.78‰和+0.63‰～ +7.93‰,二叠系煤系地层有机质δ34S值为-7.40‰～+4.00‰,均显著偏轻.此外,下寒武统黑色泥岩普遍含有较丰富的伽玛蜡烷、三芳甾烷、芳基类异戊二烯烃和惹烯,三芴系列中硫芴含量极高,其它几套黑色泥岩则不合或贫含三芳甾烷和惹烯,伽玛蜡烷和硫芴含量亦较低.综合认为油苗具相同来源,且均与研究区下寒武统黑色泥岩具有较好亲缘关系.     

Sulfur isotopes of the Nairne Pyrite deposit,South Australia

The Nairne Pyrite deposit occurs in at least five horizons in a succession of graywackes, quartzites, and siltstones of Cambrian age. Pyrite and pyrrhotite have been traced along bedding planes for almost 100 km suggesting, of course, a syngenetic origin for the sulfides. Sulfur isotopic analyses of samples from the Nairne Pyrite open-cut project provide S³⁴ values ranging from –12.8 to –20.6 permil. Such enrichment in S³², even though the spread in S³⁴ values is comparatively narrow, is suggestive of bacteriogenic sulfur which corroborates the geological evidence that the deposit is bacteriogenic — syngenetic in origin.

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Zusammenfassung Die Pyrit-Lagerstätte Nairne umfaßt wenigstens fünf Horizonte cambrischer Grauwacken, Quartzite und feine Sand- bis Tonsteine. Pyrit und Magnetkies sind über eine Distanz von fast 100 km schichtgetreu, was auf einen syngenetischen Ursprung der Sulfide hinweist. Schwefelisotop-Analysen von Pyrit aus dem Tagebau-Projekt erstrecken sich über einen S³⁴-Bereich von –12,8 bis –20,6 Promille. Diese Anreicherung weist auf einen bakteriellen Ursprung des Schwefels hin, obgleich die Spannweite der Resultate sehr eng ist. Somit ist die Feldvermutung einer syngenetisch-bakteriellen Entstehung bekräftigt.

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The isotopic analyses included in this paper were supported through the U. S. Atomic Energy Commission Contract AT (11-1) 1553, for which we are most grateful.     

Chromium,chromium isotopes and selected trace elements,western Mojave Desert,USA

Chromium(VI) concentrations in excess of the California Maximum Contaminant Level (MCL) of 50 μg/L occur naturally in alkaline, oxic ground-water in alluvial aquifers in the western Mojave Desert, southern California. The highest concentrations were measured in aquifers eroded from mafic rock, but Cr(VI) as high as 27 μg/L was measured in aquifers eroded from granitic rock. Chromium(VI) concentrations did not exceed 5 μg/L at pH < 7.5 regardless of geology. δ⁵³Cr values in native ground-water ranged from 0.7 to 5.1‰ and values were fractionated relative to the average δ⁵³Cr composition of 0‰ in the earth’s crust. Positive δ⁵³Cr values of 1.2 and 2.3‰ were measured in ground-water recharge areas having low Cr concentrations, consistent with the addition of Cr(VI) that was fractionated on mineral surfaces prior to entering solution. δ⁵³Cr values, although variable, did not consistently increase or decrease with increasing Cr concentrations as ground-water flowed down gradient through more oxic portions of the aquifer. However, increasing δ⁵³Cr values were observed as dissolved O₂ concentrations decreased, and Cr(VI) was reduced to Cr(III), and subsequently removed from solution. As a result, the highest δ⁵³Cr values were measured in water from deep wells, and wells in discharge areas near dry lakes at the downgradient end of long flow paths through alluvial aquifers. δ⁵³Cr values at an industrial site overlying mafic alluvium having high natural background Cr(VI) concentrations ranged from −0.1 to 3.2‰. Near zero δ⁵³Cr values at the site were the result of anthropogenic Cr. However, mixing with native ground-water and fractionation of Cr within the plume increased δ⁵³Cr values at the site. Although δ⁵³Cr was not necessarily diagnostic of anthropogenic Cr, it was possible to identify the extent of anthropogenic Cr at the site on the basis of the δ⁵³Cr values in conjunction with major-ion data, and the δ¹⁸O and δD composition of water from wells.     

Sulfur isotopes and origin of some sulfide deposits,New England,Australia

The S-isotopic compositions of sulfide deposits from Steinmann, granitoid and felsic volcanic associations have been examined. Ores of Steinmann association have ³⁴S values close to zero per mil (³⁴S=+0.3±3.1) it appears they are of mantle origin. Isotopically, ores of granitoid association regularly show a variable enrichment in ³²S relative to meteoritic (³⁴S=–2.7±3.3). The composition is in accord with an upper mantle/lower crustal source. Two stratiform accumulations of felsic volcanic association show a narrow spread of ³⁴S values (+0.2 to 2.4); a mantle origin for the sulfur in these deposits is favored. In contrast, vein, stockwork and cement ores are moderately enriched in ³²S relative to meteoritic (³⁴S=–4.0±6.4). These ores are polygenetic; sulfur and metals appear to have been leached from local country rocks where volcanogenic and biogenic sulfur predominate.     

Stable carbon isotopes in selected granitic,mafic, and ultramafic igneous rocks

Noncarbonate (combustion) and carbonate (acid decomposition) carbon were separately analyzed in 18 granitic rocks from a group of related Tertiary intrusions near Crested Butte, Colorado, and 14 mafic and ultramafic rocks from various localities in the western United States. Among the granites, carbonate carbon ranges from nil to 0.76 per cent with δC¹³-values from ?5.6 to ? 9.0‰ (vs PDB); noncarbonate carbon varies from 32–360 ppm with δC¹³-values from ?19.7 to ?26.6‰, The mafic and ultramafic rocks have carbonate carbon contents ranging from 53 ppm to about 2 per cent with δC¹³-values from + 2.9 to ?10.3‰; noncarbonate carbon varies from 26 to 150 ppm with δC¹³-values of ?22.2 to ? 27.l‰ For these samples, carbonate carbon ranges from 12.0 to 29.4‰ heavier than coexisting noncarbonate carbon. This consistent difference between δC¹³ of carbonate and noncarbonate carbon may be an isotopic fractionation effect. Because the specific indigenous form of noncarbonate (combustion) carbon is in doubt, conclusive interpretations regarding isotopic equilibration and fractionation cannot be made.These results have bearing on the assessment of the isotopic composition of mantle carbon and consequently are germane to the question of the origin (source) and history of crustal carbon. If mantle carbon is isotopically similar to noncarbonate (combustion) carbon, i.e. δC¹³-values from ?19.7 to ? 27.1‰, then a simple mantle degassing source for crustal carbon is improbable. Such a result would indicate an additional source of crustal carbon such as from a primitive atmosphere or extra-terrestrial accretion.     

Holocene hydrological reconstructions from stable isotopes and paleolimnology, Cordillera Real, Bolivia

Multiproxy analyses of sediment cores from Lago Taypi Chaka Kkota (LTCK) Cordillera Real, Bolivia, provide a record of drier conditions following late Pleistocene deglaciation culminating in pronounced aridity between 6.2 and 2.3 ka B.P. Today LTCK is a glacial-fed lake that is relatively insensitive to changes in P–E because it is largely buffered from dry season draw-down through the year-round supply of glacial meltwater. This was not the case during the middle to late Holocene when glaciers were absent from the watershed. Lake-water δ¹⁸O values inferred from δ¹⁸O analysis of sediment cellulose range from −12.9 to −5.3‰ and average −8.7‰ between 6.2 and 2.3 ka B.P. Modern lake-water δ¹⁸O from LTCK averages −14.8‰ which is compatible with the δ¹⁸O_lw value of −14.3‰ for the surface sediment cellulose. Analyses of δ¹⁸O from modern surface waters in 23 lakes that span the range from glacial-fed to closed basin vary from −16.6 to −2.5‰. This approximates the magnitude of the down-core shift in δ¹⁸O_lw values in LTCK during the middle to late Holocene from −12.9 to −5.3‰. Strong paleohydrologic change during the middle Holocene is also evident in diatom assemblages that consist of shallow-water, non-glacial periphytic taxa and bulk organic δ¹³C and δ¹⁵N that show increases likely resulting from degradation of lacustrine organic matter periodically exposed to subaerial conditions. Neoglaciation began after 2.3 ka B.P. as indicated by changes in the composition of the sediments, lower δ¹⁸O values, and a return to diatom assemblages characteristic of the glacial sediments that formed during the Late Pleistocene. Collectively, these data indicate that the past 2.3 ka B.P. have been the wettest interval during the Holocene. Millennial-scale shifts in the paleohydrologic record of LTCK during the early to middle Holocene conform to other regional paleoclimatic time-series, including Lake Titicaca and Nevado Sajama, and may be driven by insolation and resultant changes in atmospheric circulation and moisture supply. In contrast, an apparent 1200-year lag in the onset of wetter conditions at LTCK (2.3 ka B.P.) compared to Lake Titicaca (3.5 ka B.P.) provides evidence for variable sub-regional hydrologic response to climate change during the middle to late Holocene.     

Stable isotopes in mineralogy

Stable isotope fractionations between minerals are functions of the fundamental vibrational frequencies of the minerals and therefore bear on several topics of mineralogical interest. Isotopic compositions of the elements H, C, O, Si, and S can now be determined routinely in almost any mineral. A summary has been made of both published and new results of laboratory investigations, analyses of natural materials, and theoretical considerations which bear on the importance of temperature, pressure, chemical composition and crystal structure to the isotopic properties of minerals. It is shown that stable isotope studies can sometimes provide evidence for elucidating details of crystal structure and can be a powerful tool for use in tracing the reaction paths of mineralogical reactions.     

四川会理拉拉IOCG矿床萤石氢氧同位素特征研究

正氢、氧(H、O)同位素在地质学领域被广泛应用于成矿流体的来源与演化方面的研究(郑永飞等,2000, Deng J et al., 2009),其同位素值可用于直接与自然界水组成范围进行比较,由此指示从成矿早阶段到晚阶段流体的混合特征(徐九华等,2011)。四川拉拉IOCG矿床位于扬子地块西南缘,矿区地层主要包括:下元古界河口群(Pt_1hk)、会理群通安组(Pt_1t)、上三叠统白果湾组(T_3b,图1)。     

陕西渭北东部岩溶水环境同位素

陕西渭北东部岩溶水系统是一个复杂的地下水系统，碳酸盐岩大面积隐伏与深埋。使用传统手段和方法勘查岩溶地下水和研究可持续开发利用方案遇到诸多困难，不仅费时，而且耗资大。本文通过系统分析研究陕西渭北东部地区岩溶地下水T、D、^180、^14C环境同位素特征，揭示岩溶水的补给迳流排泄条件、岩溶水系统边界性质以及岩溶水与黄河洛河地表水、黄河岩溶泉与洛河岩溶泉之间的补排关系。结果显示环境同位素方法简便有效，能够达到预期目的。     

Stable carbon isotopes of graphite from Bogala Mine,Sri Lanka

The ratios of the carbon isotopes ¹³C and ¹²C of twenty-four graphite samples from Bogala Mine, Sri Lanka have been determined. The graphites are isotopically very similar (mean value $\text{?7.76? °}{}^{13}\text{C}{}_{\mathrm{PDB}}$; range $\text{<2?}$). Three models for the biogenic or abiogenic origin of the graphite deposit are discussed.     

Environmental isotopes in determining groundwater flow systems, northern part of Epirus, Greece

On the basis of the isotopic composition of water in the northern part of Epirus, Greece, from springs at different altitudes with well-defined recharge areas, the altitude effect on the δ¹⁸O value of groundwater is –0.142±0.003ö (100?m)^–1 and is uniform over the entire study area. Using the δ¹⁸O composition of surface water and groundwaters, the contribution of Ioannina Lake and the channel draining the lake water to the Kalamas River to the recharge of springs and boreholes was confirmed and quantitatively defined. In contrast, the Voidomatis and Vikos Rivers are not sources for recharge of the big springs along their banks. However, water from the Aoos River does replenish the aquifer in the unconsolidated deposits underlying the plain of Konitsa. In addition, limestones of Senonian–Late Eocene ages, dolomites, and limestones of the "Vigles" facies are hydraulically interconnected, and the limestones of the "Pantokrator" facies are hydraulically isolated from the other carbonate formations.     

Sulphur isotopes from the gruvåsen sulphide skarn deposit,Bergslagen, Sweden

Summary The Gruvåsen sulphide skarns in Western Bergslagen are hosted by a sequence of marbles and metacherts, intruded by a number of thin mafic sills and dykes of midProterozoic age. The sulphide skarns show a zonal distribution with Cu-Zn-Fesulphide-rich pyroxene skarns (± scheelite, molybdenite, cassiterite, bismuth) in the central, and Zn-Fe-Pb-As-sulphide-rich amphibole skarns in the peripheral zones of mineralization. The sulphide skarns in the central zone are closely related to a phase of local potassic alteration that affected the marbles, cherts and mafic intrusions. ³⁴S values of sulphides range between + 0.5 and + 1.3% for the central zone, and between-1.4 and + 1.5% for the peripheral zone. Sulphide-pair sulphur isotope geothermometry (Ohmoto and Rye, 1979) yields temperatures around 555°C corresponding with the temperature of 550–600°C estimated from silicate and sulphide parageneses. Although the Gruvâsen deposit is situated close to the Filipstad-type granitic intrusion, this granite is unlikely to have a genetic relationship with the sulphide mineralization, because the sulphide skarns were deformed at about 1,860 Ma, whereas the postkinematic Filipstad-type granite is dated at +- 1,640Ma (Oen, 1982). Hydrothermal fluids at estimated temperatures around 550°C, presumably heated by the coeval solidifying mafic sills and dykes, are considered responsible for the dissolution and transport of sulphur from the mafic rocks, and of metals from both mafic and felsic rocks underlying the Gruvåsen marbles, and for the redeposition of metals and sulphur in the Gruvåsen sulphide skarn deposit.

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Schwefelisotopen der Gruvåsen Sulfid-Skarnlagerstätte, Bergslagen, Schweden

Zusammenfassung Die sulfidischen Skarne von Gruvåsen, West-Bergslagen, sitzen in Mergeln and Metaquarziten auf, die von zahlreichen mitelproterozoischen, geringmächtigen mafischen Sills und Gängen durchdrungen werden. Die Sulfid-Skarne sind zoniert. Im zentralen Bereich der Mineralisation treten Cu-Zn-Fe-sulfidreiche Pyroxen-Skarne auf (+- Scheelit, Molybdenit, Cassiterit, Wismuth), während die Randzonen vorwiegend aus Zn-Fe-Pb-As-sulfidreichen Amphibol-Skarnen bestehen. Die zentralen Skarnanteile zeigen engen Zusammenhang mit einer lokalen K-Alteration der Mergel, Metaquarzite und mafischen Intrusionen. In der zentralen Zone liegen die ³⁴ S-Werte der Sulfide zwischen + 0.5 und + 1.3%, in der Randzone zwischen - 1.43 und + 1.5%. SchwefelisotopenGeothermometrie von Sulfidpaaren (Ohmoto & Rye, 1979) ergaben Temperaturen um 550°C. Diese stimmen mit den Temperaturen aus den Silikat- und Sulfidparagenesen von 550–600°C gut überein. Obwohl die Gruvåsen Lagerstätte nahe der FilipstadTyp Granitintrusion liegt, erscheint eine genetische Verbindung mit der Sulfidmineralisation unwahrscheinlich, da die Sulfid-Skarne ein Deformationsalter von 1860 Mio zeigen, während der postkinematische Filipstad-Typ Granit auf +- 1640 mio datiert ist (Oen, 19982). Es wird vermutet, daß hydrothermale Lösungen, die durch die erstarrenden mafischen Sills und Gänge auf etwa 550°C aufgeheizt worden sind, für die Vererzung verantwortlich sind. Der Schwefel kann aus den mafischen Gesteinen bezogen werden, die Metalle aus mafischen und felsischen Gesteinen, die die Gruvåsen Mergel unterlagern. Hydrothermale Aktivität verursachte Lösung, Transport und Umlagerung des Schwefels und der Metalle in die Gruväsen Sulfid-Skarn Lagerstätte.

     

The Kaidun chondrite breccia: Petrology, oxygen isotopes, and trace element abundances

Oxygen isotope and trace element data for 13 samples of the Kaidun chondritic breccia reaffirm the complex polymict nature of this unique meteorite. Bulk Kaidun samples most closely resemble CR chondrites, but the matrix is CI-like. Two separated clasts are CR-like but have some properties that resemble CM, two clasts are enstatite chondrites (one EL and one EH), one clast is an aubrite-like metal-rich impact melt, and one clast is a unique layered olivine-bearing pyroxenite with the isotopic composition of an aubrite. Yet, although each clast resembles a known meteorite group, all deviate in some respect from the norms for those groups. Collectively, Kaidun has sampled materials not yet represented in the world meteorite collections and which greatly extend the definitions of known meteorite groups. Phyllosilicates in Kaidun span a very wide range in composition and vary from clast to clast, suggesting that the aqueous alteration experienced by the clasts predated assembly of the Kaidun parent body.     

石碌钴-铜矿床流体包裹体和稳定同位素特征及成因

海南石碌钴-铜矿体赋存于石碌群第六层的下段,即介于铁矿体与石碌群第五层片岩之间的含钴-铜层位中,容矿岩石主要为白云岩、透辉石透闪石化白云岩。钴-铜矿床的形成经历了海底喷溢沉积期、石英-硫化物期(热液期)和表生期。海底喷溢沉积期石英包裹体均一温度变化于112~205℃,多集中在130~205℃;盐度w(NaCl_eq)为1.74%~6.59%;密度变化于0.88~0.95 g/cm³。温度范围与很多古代沉积喷流矿床及正在活动的海底热液成矿作用的温度相似,盐度低于曾报道的多数沉积喷流矿床的流体包裹体盐度值, 但与那些同为低密度成矿流体的喷流沉积矿床极为相近。海底喷溢沉积期形成的硬石膏δ³⁴S值为+21.4‰~+21.8‰,平均值为+21.6‰,强烈富集重硫,硬石膏δ³⁴S值代表着新元古代石碌群沉积时海水的δ³⁴S值。石英-硫化物期石英、白云石和方解石均一温度多集中在170~270℃;盐度w(NaCl_eq)为1%~7%;密度变化于0.88~0.95 g/cm³。成矿流体属于中温低盐度流体。石英-硫化物期成矿流体δD值为-63‰~-83‰,成矿流体δ¹⁸O_水值变化于1.3‰~6.8‰之间,指示成矿流体来源于岩浆,成矿后期有大气降水的加入。石英-硫化物期硫化物δ³⁴S值为+8.1‰~+21.2‰,硫源来源于石碌群中蒸发岩的溶解作用。石碌钴-铜矿床属中温热液充填交代矿床,与矿床周围花岗质岩浆活动有关。     

Fossil pollen, molluscs, and stable isotopes in the Dättnau valley, Switzerland

Pollen and mollusc deposits in a sedimentation series laid down in the Dattnau valley during the Late Glacial and early Post-glacial were studied. For the first time δ¹³C and δ¹⁸O in land-snail shells were measured. It was possible to reconstruct vegetational and climatic developments from the Bölling ( c . 12,500 B.P.) until well into the early Boreal ( c . 9,000 B.P.). The two sets of findings agree well. The Late Glacial is seen to comprise two intervals: the continuous, locally rather moist, warm Bölling/Alleröd period, and the subsequent dry . cold Younger Dryas. The profile ceases after the changeover from the Late Glacial to the Post-glacial. The transitions from the Alleröd to the Younger Dryas and hence to the Preboreal and Boreal are both clearly identifiable in the pollen diagram; the mollusc record, however, ceases to be interpretable shortly before the climatic change to the Post-glacial. The δ¹⁸O curve shows a clear distinction between the AllerÖd and the Younger Dryas. The Gerzensee fluctuation, immediately before this transition. is evident as a negative deviation.     

锂同位素与大陆风化

气候变化与大气二氧化碳浓度息息相关.大陆岩石圈风化是影响大气二氧化碳浓度的重要过程.通过还原陆壳古风化信息,我们可以有效地了解地球气候条件的演化历史.传统方法上,前人曾使用锶同位素示踪大陆风化,但其解释尚有不足.例如,海水锶同位素比值会受到海洋热液的影响,而河流锶同位素比值则易受风化岩石类型的影响.此外,只有硅酸盐风化被认为在长时间尺度控制着大气碳汇,但锶的碳酸盐风化却与硅酸盐风化很难分辨.因此,我们需要一种更理想的同位素体系作为示踪大陆风化历史的介质.锂,作为微量元素,主要集中在岩石圈的硅酸盐矿物中,在碳酸盐岩含量较少.所以,硅酸盐风化可以使用锂同位素予以记录.同时,锂同位素受生物分馏效应影响较小,可以在海相碳酸盐岩中保存良好.这些优势为海相碳酸盐岩的锂同位素信号示踪大陆风化历史提供了有力支撑,但我们仍需对风化、迁移和结晶等过程的锂同位素地球化学行为有清晰的认识.为此,本文回顾不同储库的锂同位素组成以及各物相间锂元素配分和同位素分馏特征,总结了近年来锂同位素在重建大陆风化历史方面的进展,并详述了有待解决的关键问题.