230Th/234U dating of Holocene tufas: possibilities and problems

High-resolution chronologies in continental carbonate deposits such as tufas are required for detailed palaeoclimatic and environmental studies. This work set out to establish if high-resolution U-series dating of detritus-rich Holocene tufas is routinely possible. The study centres on a paludal Holocene tufa from southern England that already has an existing Holocene chronology, based on ¹⁴C and supported by biostratigraphy, against which to compare U-series dates. The results show that significant detrital contamination combined with low initial U concentrations, and short time for ingrowth of radiogenic ²³⁰Th make high-resolution U-series dating of Holocene tufa very difficult. Moreover, a single (²³⁰Th/²³²Th)_initial value to correct for the presence of detrital ²³⁰Th is not appropriate at the study site, a finding that may apply to most Holocene tufas. Total sample dissolution of coeval samples demonstrates considerable variability in the isotopic composition of the detritus. The total sample dissolution data are too scattered to constrain chronologies at the required resolution and may indicate the incorporation of a ²³⁰Th-rich component in the detritus.     

C and Th/U dating of Pleistocene and Holocene stromatolites from East African paleolakes

During recent humid episodes, stromatolites were built along paleolake margins, some 60 m above the modern water level of Lakes Natron and Magadi (southern Gregory Rift Valley). Three generations of stromatolites are observed, the more recent ones frequently covering pebbles and boulders eroded from the older ones. The youngest one yielded ¹⁴C ages ranging from approximately 12,000 to 10,000 yr B.P. Their δ¹³C values (≥2.6%) suggest isotopic equilibrium between the paleolake total inorganic dissolved carbon and the atmospheric CO₂, thereby lending credence to the reliability of the ¹⁴C. An initial ²³⁰Th/²³²Th ratio in the detrital component was determined by Th/U measurements on the ¹⁴C dated stromatolites. Using this value a ²³⁰Th/²³⁴U chronology for the older stromatolites was calculated. Ages of ≥240,000 and 135,000 ± 10,000 yr were obtained for the first and second generations, respectively. A humid episode apparently characterized eastern Africa during each glacial-interglacial transition. ¹⁸O and ¹³C measurements on stromatolites, when compared to values on modern waters and carbonates, provide paleohydrological information. Long residence time of the paleolake waters and less seasonally contrasted regimes are inferred.     

TIMS测定铀矿石样品中^234U/^238U、^230Th/^232Th、^228Ra/^226Ra的方法研究

研究了TIMS测定铀矿石样品中234U/238U、230Th/232Th、228Ra/226Ra的方法。建立了铀矿石密闭混酸一次溶样的方法和采用阴离子、阳离子和Sr特效树脂逐级离子交换分离纯化U、Th和Ra的流程,满足了TIMS测量要求。测定结果表明：100～1000 ng的天然铀中234U/238U,其测量精密度从静态多接收的2.34%提高到动态多接收的0.47%;对230Th与232Th丰度接近、质量为1μg左右的钍,采用三带点样技术和法拉第多接收技术测定230Th/232Th,其内精度平均值为0.0048%,外精度为0.028%;采用单带加钽发射剂,ETP跳峰测定50～100 fg镭-228稀释剂中的228Ra/226Ra,其内精度小于0.10%,外精度小于0.20%。比较TIMS和HR-ICP-MS、α能谱法测定234U/238U、230Th/232Th、228Ra/226Ra结果,三者结果相吻合。TIMS测量法样品用量少、快速、准确、精密度高,是U、Th、Ra同位素比值测定方法的又一补充。     

Radiocarbon dating of shells from marine Holocene deposits in the Disko Bugt area, West Greenland

Shells were collected from marine sediments in the area youth of Disko Bugt from various altitudes up to 50 m. Radiocarbon dates showed that only some of the shells were from sands and gravels formed at or near sea level and could be used to date the land/sea level changes. The shell dates show a regression from about 43 m at 7000 B.P. to about 8 m at 4000 B.P. All sediments with shells are Holocene in age, the oldest date being nearly 9000 B.P. The date of the Fjord Stage moraine in Orpigsoq is estimated at about 8000 B.P. on the basis of the altitude of the marine limit at 62 m. Extrapolations dated the older marine limits, falling from an altitude of 130 m to 80 m, at about 11,000 B.P. to 9000 B.P. These are approximate dates for the deglaciation of the area outside the Fjord Stage moraine. The distribution of shells in the sediments was shown to be largely dependent on habitat and water depth. At least some changes ill fauna were caused by a decrease of water depth due to the relative uplift of land. No tilting or warping of the land surface could he detected in the at-ea about 100 km long from the coast towards the Inland Ice.     

Precise two chronometer dating of Pleistocene travertine: The Th/U and Raex/Ra(0) approach

In order to determine the geochemical evolution of a freshwater limestone cave system located in central Switzerland (Hell Grottoes at Baar/Zug,) young postglacial tufaceous limestone and travertine precipitates were investigated using the ²³⁰Th/²³⁴U ingrowth system. Additional analyses of further radionuclides within the ²³⁸U decay chain, i.e. ²²⁶Ra and ²¹⁰Pb, showed that the Th/U chronometer started with insignificant inherited ²³⁰Th over the entire formation period of the travertine setting (i.e. ²³⁰Th(0)=0). A contribution from detrital impurities with ²³⁰Th/²³⁴U in secular equilibrium could be precisely subtracted by applying isochron dating of cogenetic phases and recently formed travertine. The resulting precise ²³⁰Th/²³⁴U formation ages were found to be consistent with the geological stratigraphy and were furthermore used to demonstrate the applicability of the next geologically important chronometer in the ²³⁸U-decay series, based on decay of excess ²²⁶Ra normalized to the initial, i.e.²²⁶Ra_ex/²²⁶Ra(0). This system is suitable for dating phases younger than 7000 yr when the correction of a detritus component increasingly limits the precision of the ²³⁰Th/²³⁴U chronometer. Analytical solutions of the coupled ²³⁴U/²³⁰Th/²²⁶Ra radionuclide system predicted that the ²²⁶Ra_ex/²²⁶Ra(0) chronometer is independent of the actual ²³⁰Th activity build up from decay of ²³⁴U, if the systems starts with zero inherited ²³⁰Th(0). The data set confirmed this hypothesis and showed furthermore that the initially incorporated ²²⁶Ra excess must have remained almost uniform in all limestone over a period of at least 7000 yr, i.e. 4–5 half-lives of ²²⁶Ra. This is concluded because (i) the ²²⁶Ra_ex/²²⁶Ra(0) ages agreed well with those derived from ²³⁰Th/²³⁴U, (ii) all data plot within uncertainty on the ²²⁶Ra_ex/²²⁶Ra(0) decay curve and (iii) the atomic Ba/Ca ratio was found to be constant in the travertine material independent of the sample ages. Provided that such boundary conditions hold, ²²⁶Ra_ex/²²⁶Ra(0) should be applicable to materials which are suitable for ²³⁰Th/²³⁴U dating in sedimentology and oceanography, i.e. travertine, corals, phosphorites, etc., and should strongly support ²³⁰Th/²³⁴U for samples that have been formed a few thousand years ago.     

Factors controlling the groundwater transport of U, Th, Ra, and Rn

A model for the groundwater transport of naturally occurring U, Th, Ra, and Rn nuclides in the²³⁸U and²³²Th decay series is discussed. The model developed here takes into account transport by advection and the physico-chemical processes of weathering, decay, α-recoil, and sorption at the water-rock interface. It describes the evolution along a flowline of the activities of the²³⁸U and²³²Th decay series nuclides in groundwater. Simple sets of relationships governing the activities of the various species in solution are derived, and these can be used both to calculate effective retardation factors and to interpret groundwater data. For the activities of each nuclide, a general solution to the transport equation has been obtained, which shows that the activities reach a constant value after a distance ϰ_i, characteristic of each nuclide. Where ϰ_i is much longer than the aquifer length, (for²³⁸U,²³⁴U, and²³²Th), the activities grow linearly with distance. Where gKⁱ is short compared to the aquifer length, (for²³⁴Th,²³⁰Th,²²⁸Th,²²⁸Ra, and²²⁴Ra), the activities rapidly reach a constant or quasi-constant activity value. For²²⁶Ra and²²²Rn, the limiting activity is reached after 1 km. High δ²³⁴U values (proportional to the ratio^ɛ234Th/^W238U) can be obtained through high recoil fraction and/or low weathering rates. The activity ratios²³⁰Th/²³²Th,²²⁸Ra/²²⁶Ra and²²⁴Ra/²²⁶Ra have been considered in the cases where either weathering or recoil is the predominant process of input from the mineral grain. Typical values for weathering rates and recoil fractions for a sandy aquifer indicate that recoil is the dominant process for Th isotopic ratios in the water. Measured data for Ra isotope activity ratios indicate that recoil is the process generally controlling the Ra isotopic composition in water. Higher isotopic ratios can be explained by different desorption kinetics of Ra. However, the model does not provide an explanation for²²⁸Ra/²²⁶Ra and²²⁴Ra/²²⁶Ra activity ratios less than unity. From the model, the highest²²²Rn emanation equals 2ɛ. This is in agreement with the hypothesis that²²²Rn activity can be used as a first approximation for input by recoil (Krishnaswamiet al 1982). However, high²²²Rn emanation cannot be explained by production from the surface layer as formulated in the model. Other possibilities involve models including surface precipitation, where the surface layer is not in steady-state.     

Ra/Ra and Ra/Ba ratios to track barite formation and transport in the water column

We measured ²²⁸Ra_ex/²²⁶Ra_ex and ²²⁶Ra_ex/Ba_ex ratios in suspended and sinking particles collected at the Oceanic Flux Program (OFP) time-series site in the western Sargasso Sea and compared them to seawater ratios to provide information on the origin and transport of barite (BaSO₄) in the water column. The ²²⁸Ra_ex/²²⁶Ra_ex ratios of the suspended particles down to 2000 m are nearly identical to those of seawater at the same water depth. These ratios are much lower than expected if suspended barite was produced in surface waters and indicate that barite is produced throughout the mesopelagic layer. The ²²⁸Ra_ex/²²⁶Ra_ex activity ratios of sinking particles collected at 1500 and 3200 m varied mostly between 0.1 and 0.2, which is intermediate between the seawater ratio at these depths (<0.03) and the seawater ratios found in the upper 250 m (0.31-0.42). This suggests that excess Ba (i.e., Ba_ex = Ba_total − Ba_lithogenic), considered to be mainly barite, present in the sinking flux is a mixture of crystals formed recently in the upper water column, formed several years earlier in the upper water column, or formed recently in deeper waters. We observe a sizeable temporal variability in the ²²⁸Ra_ex/²²⁶Ra_ex ratios of sinking particles, which indicates temporal variability in the relative proportion of barite crystals originating from surface (with a high ²²⁸Ra_ex/²²⁶Ra_ex ratio) and mesopelagic (with a low ²²⁸Ra_ex/²²⁶Ra_ex ratio) sources. However, we could not discern a clear pattern that would elucidate the factors that control this variability. The ²²⁶Ra/Ba ratios measured in seawater are consistent with the value reported from the GEOSECS expeditions (2.3 dpm μmol⁻¹) below 500 m depth, but are significantly lower in the upper 500 m. High ²²⁶Ra_ex/Ba_ex ratios and elevated Sr concentrations in suspended particles from the upper water column suggest preferential uptake of ²²⁶Ra over Ba during formation of SrSO₄ skeletons by acantharians, which must contribute to barite formation in shallow waters. Deeper in the water column the ²²⁶Ra_ex/Ba_ex ratios of suspended particles are lower than those of seawater. Since ²²⁸Ra_ex/²²⁶Ra_ex ratios demonstrate that suspended barite at these depths has been produced recently and in situ, their low ²²⁶Ra_ex/Ba_ex ratios indicate preferential uptake of Ba over Ra in barite formed in mesopelagic water.     

Ra/Ra and Ra/Ba ratios in the Western Mediterranean Sea: Barite formation and transport in the water column

²²⁶Ra, ²²⁸Ra and Ba distributions as well as ²²⁸Ra/²²⁶Ra and ²²⁶Ra/Ba ratios were measured in seawater, suspended and sinking particles at the DYFAMED station in the Western Mediterranean Sea at different seasons of year 2003 in order to track the build-up and fate of barite through time. The study of the ²²⁸Ra_ex/²²⁶Ra_ex ratios (Ra_ex = Ra activities corrected for the lithogenic Ra) of suspended particles suggests that Ba_ex (Ba_ex = Ba concentrations corrected for the lithogenic Ba, mostly barite) formation takes place not only in the upper 500 m of the water column but also deeper (i.e. throughout the mesopelagic layer). Temporal changes in the ²²⁸Ra_ex/²²⁶Ra_ex ratios of sinking particles collected at 1000 m depth likely reflect changes in the relative proportion of barite originating from the upper water column (with a high ²²⁸Ra/²²⁶Ra ratio) and formed in the mesopelagic layer (with a low ²²⁸Ra/²²⁶Ra ratio). ²²⁸Ra_ex/²²⁶Ra_ex ratios measured in sinking particles collected in the 1000 m-trap in April and May suggest that barite predominantly formed in the upper water column during that period, while barite found outside the phytoplankton bloom period (February and June) appears to form deeper in the water column. Combining ratios of both the suspended and sinking particles provides information on aggregation/disaggregation processes. High ²²⁶Ra_ex/Ba_ex ratios were also found in suspended particles collected in the upper 500 m of the water column. Because celestite is expected to be enriched in Ra [Bernstein R. E., Byrne R. H. and Schijf J. (1998) Acantharians: a missing link in the oceanic biogeochemistry of barium. Deep-Sea Res. II45, 491-505], acantharian skeletons may contribute to these high ratios in shallow waters. The formation of both acantharian skeletons and barite enriched in ²²⁶Ra may thus contribute to the decrease in the dissolved ²²⁶Ra activity and ²²⁶Ra/Ba ratios of surface waters observed between February and June 2003 at the DYFAMED station.     

The age of Upper Pleistocene marine deposits of the Boreal transgression on the basis of electron-spin-resonance (ESR) dating of subfossil mollusc shells

The potential use of a new ESR method for the dating of subfossil shells is discussed on an example from the northern part of the East-European Plain. A variant of the ESR technique, elaborated at the Institute of Geology of the Academy of Sciences of the Estonian SSR, is described and the Eemian age of the Boreal transgression proved.     

Reconstructing seawater column 90Sr based upon 210Pb/226Ra disequilibrium dating of mollusk shells

The shells of marine and fresh water mollusks can serve as effective archives in retrieving information on natural and anthropogenic environmental changes. The advantage of using bivalves is that they integrate water chemistry changes into their shells during their life span. Retrospective study of environmental changes and pollutants using bivalve shells requires precise determination of the time of incorporation into the abiotic environmental matrix (here after age) of the specimen. For the first time, a set of archived bivalve samples (for which date of the death/collection is known) has been analyzed to establish the ages of mollusk shells using the ²¹⁰Pb–²²⁶Ra disequilibrium method. In addition, Sr and ⁹⁰Sr were analysed. The ages obtained using the ²¹⁰Pb/²²⁶Ra disequilibrium dating method agrees well with the calendar years calculated from the date of death/collection. The ages obtained can be utilized to reconstruct the ⁹⁰Sr levels in the water column at sites where the mollusk shells were collected.     

Radiocarbon dating of marine shells, including a discussion of apparent age of Recent shells from Norway

General problems in determining and interpreting shell C¹⁴ dates are discussed: calculation methods, factors influencing primary activity (apparent age), and determination of contamination. It is concluded that shell dates are reliable when handled carefully. Measurements on ten shells, collected between 1898 and 1923 on the Norwegian coast, gave apparent ages from 340±75 to 550±80 years, indicating that apparent age is not a significant problem in dating of Norwegian shells.     

Fractionation of U,Th, Ra and Pb from boreal forest soils by sequential extractions

To determine the mobility of natural radionuclides in boreal forest soil, a five-step sequential extraction procedure was carried out on soil samples taken from various depths down to 3 m on Olkiluoto Island, Finland, where there are plans to construct a spent nuclear fuel disposal repository in the bedrock. The extracted fractions studied were exchangeable, acid-soluble, reducible, oxidizable and tightly bound. It was found that the extractability of most of the radionuclides studied was dependent on the sample grain size and depth. All the elements were concentrated in the smallest grain size samples (<0.063 mm). The extraction behaviour of Th, however, did not vary with sample depth, and only about 10% of the Th was extracted by the time of the final extraction step. Stable Pb and ²¹⁰Pb, as well as Ba and Ra concentrations were strongly correlated in the extractions. Radium and Ba were leached more readily than the other elements; approximately 17% of the total Ra was found in the first fraction extracted, representing exchangeable ions. Uranium was more mobile in the topsoil horizons than in the lower horizons. In the topsoil samples, an average of 51% of the extractable U was leached in the second extraction step, representing the elements soluble in weak acids, whereas only 13% of the U in the subsoil samples was extracted in this step. This is probably due to changes in soil redox conditions lower down the soil profile. The extraction behaviour of Pb and Fe also suggests the presence of more reducing conditions in the deeper soil horizons, because the percentage of extractable Pb and Fe in the oxidizable fraction increased with sample depth.     

Dating fluvial terraces by Th/U on pedogenic carbonate, Wind River Basin, Wyoming

Reliable and precise ages of Quaternary pedogenic carbonate can be obtained with ²³⁰Th/U dating by thermal ionization mass spectrometry applied to carefully selected milligram-size samples. Datable carbonate can form within a few thousand years of surface stabilization allowing ages of Quaternary deposits and surfaces to be closely estimated. Pedogenic carbonate clast-rinds from gravels of glacio-fluvial terraces in the Wind River Basin have median concentrations of 14 ppm U and 0.07 ppm ²³²Th, with median (²³⁰Th/²³²Th) = 270, making them well suited for ²³⁰Th/U dating. Horizons as thin as 0.5 mm were sampled from polished slabs to reduce averaging of long (≥10⁵ yr), and sometimes visibly discontinuous, depositional histories. Dense, translucent samples with finite ²³⁰Th/U ages preserve within-rind stratigraphic order in all cases. Ages for terraces WR4 (167,000 ± 6,400 yr) and WR2 (55,000 ± 8600 yr) indicate a mean incision rate of 0.26 ± 0.05 m per thousand years for the Wind River over the past glacial cycle, slower than inferred from cosmogenic-nuclide dating. Terrace WR3, which formed penecontemporaneously with the final maximum glacial advance of the penultimate Rocky Mountain (Bull Lake) glaciation, has an age of 150,000 ± 8300 yr indicating that it is broadly synchronous with the penultimate global ice volume maximum.     

Single Column Sequential Extraction of Ra,Nd, Th,Pa and U from a Natural Sample

A new procedure allowing the sequential extraction of Ra, Nd, Th, Pa and U from the same initial natural sample (sea or river waters, particles, sediments, rocks) is proposed. Extraction recoveries were better than 90%. Procedural blanks ranged from 80 pg (for Nd) to below 1 fg, the detection limit of the MC‐ICP‐MS used (for Pa); all were negligible compared with the amounts of elements currently determined. Based on classical anionic resins attached to a peristaltic pump allowing precise flow rate control, this procedure allowed a consequent reduction of the sample size, which improved the sampling resolution and reduced the sampling cost. It also ensured a better consistency of the samples for the five tracers.     

Seawater nutrient and carbonate ion concentrations recorded as P/Ca, Ba/Ca, and U/Ca in the deep-sea coral Desmophyllum dianthus

As paleoceanographic archives, deep sea coral skeletons offer the potential for high temporal resolution and precise absolute dating, but have not been fully investigated for geochemical reconstructions of past ocean conditions. Here we assess the utility of skeletal P/Ca, Ba/Ca and U/Ca in the deep sea coral D. dianthus as proxies of dissolved phosphate (remineralized at shallow depths), dissolved barium (trace element with silicate-type distribution) and carbonate ion concentrations, respectively. Measurements of these proxies in globally distributed D. dianthus specimens show clear dependence on corresponding seawater properties. Linear regression fits of mean coral Element/Ca ratios against seawater properties yield the equations: P/Ca_coral (μmol/mol) = (0.6 ± 0.1) P/Ca_sw(μmol/mol) - (23 ± 18), R² = 0.6, n = 16 and Ba/Ca_coral(μmol/mol) = (1.4 ± 0.3) Ba/Ca_sw(μmol/mol) + (0 ± 2), R² = 0.6, n = 17; no significant relationship is observed between the residuals of each regression and seawater temperature, salinity, pressure, pH or carbonate ion concentrations, suggesting that these variables were not significant secondary dependencies of these proxies. Four D. dianthus specimens growing at locations with Ω_arag ? 0.6 displayed markedly depleted P/Ca compared to the regression based on the remaining samples, a behavior attributed to an undersaturation effect. These corals were excluded from the calibration. Coral U/Ca correlates with seawater carbonate ion: U/Ca_coral(μmol/mol) = (−0.016 ± 0.003) (μmol/kg) + (3.2 ± 0.3), R² = 0.6, n = 17. The residuals of the U/Ca calibration are not significantly related to temperature, salinity, or pressure. Scatter about the linear calibration lines is attributed to imperfect spatial-temporal matches between the selected globally distributed specimens and available water column chemical data, and potentially to unresolved additional effects. The uncertainties of these initial proxy calibration regressions predict that dissolved phosphate could be reconstructed to ±0.4 μmol/kg (for 1.3-1.9 μmol/kg phosphate), and dissolved Ba to ±19 nmol/kg (for 41-82 nmol/kg Ba_sw). Carbonate ion concentration derived from U/Ca has an uncertainty of ±31μmol/kg (for ). The effect of microskeletal variability on P/Ca, Ba/Ca, and U/Ca was also assessed, with emphasis on centers of calcification, Fe-Mn phases, and external contaminants. Overall, the results show strong potential for reconstructing aspects of water mass mixing and biogeochemical processes in intermediate and deep waters using fossil deep-sea corals.     

环境水样中铀、钍、镭和铅同位素及其比值的系统分析

本文研究了从5L水中用铁、铅、钡和铈作载体,系统分析~(234)U、~(238)U、~(228)Th、~(230)Th~(232)Th、~(224)Ra、~(226)Ra、~(228)Ra和~(210)Pb的含量或比值。铀、钍经Fe(OH)_3沉淀富集后用TBP萃淋树脂柱分离,用激光荧光和比色法测定,同位素比值用α谱仪测量,化学回收率在90％以上,测量下限分别为1μg/L和3μg/L。镭、铅经硫酸盐沉淀富集后,用EDTA在不同pH条件下分离,~(224)Ra和~(226)Ra用射气法测定,~(228)Ra和~(210)Pb分别用其β子体~(228)Ac和~(210)Bi在低本底β装置上测量,测量下限分别为2.5×10~(-2)、8×10~(-3)、4×10~(-3)和5×10~(-3)Bq/L。     

The first case study of 230Th/U and 14C dating of mid-valdai organic deposits

From the viewpoint of precision and reliability of radioisotopic dating, deposits whose quantitative age can be determined through several methods of geochronometry are of special interest. The mutually conforming finite ¹⁴C and ²³⁰Th/U dates of buried Neopleistocene organic deposits, taken from the Tolokonka section by the North Dvina River (100 km downstream from the city of Kotlas), have been obtained for the first time in Russia. The stratigraphical reference of these results to those obtained via the optically induced luminescence for upper and lower bedding layers has been established. The presented geochronometric data have allowed us to consider the age of oxbow lake organic deposits completely reliable and refer the time of their formation to the Tyrbei warming within the MIS-3. The applicability of the new version of the ²³⁰Th/U method for dating of interglacial and interstadial deposits, for the purpose of solving the Middle and Late Neopleistocene chronostratigraphy issues, is confirmed.     

Geochemistry and U-series dating of Holocene and fossil marine hydrothermal manganese deposits from the Izu-Ogasawara arc

This study investigated Holocene and fossil hydrothermal manganese deposits in the Izu-Ogasawara arc. Mineralogically, these deposits comprise 10 Å and 7 Å manganate minerals, and the fossil samples showed higher 10 Å stabilities. Chemical compositions of the Holocene samples are typical of other hydrothermal manganese deposits, including low Fe/Mn ratios, low trace metals, and low rare earth elements. Although the fossil samples generally have similar chemical characteristics, they exhibit significant enrichment in Ni, Cu, Zn, Cd, Ba, REE, Tl, and Pb contents. Furthermore, the chondrite-normalized REE patterns showed more light REE enrichment trends. These chemical characteristics suggest post-depositional uptake of these metals from seawater. U-Th dating of a Holocene hydrothermal manganese deposit from the Kaikata Seamount indicated 8.8 ± 0.94 ka for the uppermost layer and downward growth beneath the seafloor with a growth rate of ca. 2 mm/kyr. This is approximately three orders of magnitude faster than that of hydrogenetic ferromanganese crusts. U-Pb age of a fossil hydrothermal manganese deposit from the Nishi-Jokyo Seamount showed 4.4 ± 1.6 Ma, which was contemporary with basaltic volcanism (5.8 ± 0.3 Ma). Hydrothermal manganese deposits contain high concentrations of high value Mn, but only small amounts of valuable minor metals; their ages constrain the periods of past hydrothermal activity and provide a vector to explore for polymetallic sulfide deposits.     

南京直立人的U/Th和U/Pa年代

中国直立人化石的准确定年对于研究人类演化有着极为重要的意义。1993～1994年在南京汤山葫芦洞发现的两个直立人头盖骨化石和一枚牙化石被称为“南京直立人”。其中1号头盖骨化石之上的方解石钙板的U/Th年龄为53.3_(-1.2)~(+1.5)万年;但考虑到定年的准确性,则为53.3_(-3.0)~(+3.5)万年。其~(231)Pa/~(235)U活度比值为0.998±0.006。这表明“南京直立人”的年代应该大于50万年。与”南京直立人”伴生的动物牙化石U/Th年代为18.5～29.0万年;U/Pa年代为13.7～17.2万年。此外,对于同一颗牙化石,牙釉的年龄小于牙本质的年龄。同一样品的U/Pa年龄也显著小于其U/Th年龄。因此,牙化石的U摄取过程并不符合U早期摄取模式。多数牙化石分析点在~(234)U/~(238)U-~(230)Th/~(238)U图上落在位于U早期摄取和线性摄取模式曲线之间,指示牙化石的U摄取过程很可能介于上述两种模式之间。如果这一假设成立,那么牙化石的U/Th和U/Pa线性摄取模式年龄则为其年代的上限。因为不受U摄取过程~(234)U/~(238)U变化的影响,U/Pa线性摄取模式年龄比U/Th较为可靠。最小的U/Pa线性摄取模式年龄为1Ma,这是”南京直立人”上限年龄的估计。从定年结果看,”南京直立人”可能生活在海洋同位素(MIS)16阶段,但这不是最终结论。