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1.
Uranium contents and234U/238U activity ratios have been determined for groundwaters from the Lincolnshire Limestone artesian aquifer in eastern England. Changes in the quantitative and isotopic chemistry of the dissolved uranium are explained in terms of a mixing model involving the rapidly moving fissure water and much older water stored in the pore system of this oolitic limestone. The western part of the aquifer, closest to recharge, is dominated by oxidising groundwaters which then enter a reducing zone towards the east, where there is an abrupt decrease in Eh and the chlorinity of the groundwaters begins to increase. Uranium contents in the oxidising zone range from 0.7 to 3.4 μg kg?1 and234U/238U activity ratio of this dissolved uranium is close to unity, the equilibrium value. The uranium content decreases abruptly when the grounwaaters enter the reducing zone, averaging 0.04 μg kg?1 east of the oxidation/reduction barrier. Simultaneously with the decrease in uranium content, there is an increase in234U/238U activity ratio and this ratio increases to a maximum within 7 km of the oxidation/reduction barrier. This increase in activity ratio is attributed to enhanced234U solution due to234Th recoil from uraniferous fissure surfaces east of the oxidising zone. The activity ratio of dissolved uranium in the ancient pore waters could in principle reach high values due to234Th recoil from the oolith surfaces. However, the activity ratio actually declines further east and this can only be explained as a consequence of mixing with pore waters in which the uranium activity ratio is closer to equilibrium.234Th recoil from the oolith surfaces has probably been inhibited by sealing of the uranium-bearing surfaces in the process of oolith cementation.  相似文献   

2.
The northern region of Guangdong Province, China, has suffered from the extensive mining/milling of uranium for several decades. In this study, surface waters in the region were analyzed by inductively coupled plasma optical emission spectrometry (ICP‐OES) for the concentrations of uranium (U), thorium (Th), and non‐radioactive metals (Fe, Mn, Mg, Li, Co, Cu, Ni, and Zn). Results showed highly elevated concentrations of the studied radionuclides and metals in the discharged effluents and the tailing seepage of the U mining/milling sites. Radionuclide and heavy metal concentrations were also observed to be overall enhanced in the recipient stream that collected the discharged effluents from the industrial site, compared to the control streams, and rivers with no impacts from the U mining/milling sites. They displayed significant spatial variations and a general decrease downstream away from upper point‐source discharges of the industrial site. In addition, obvious positive correlations were found between U and Th, Fe, Zn, Li, and Co (R2 > 0.93, n = 28) in the studied water samples, which suggest for an identical source and transport pathway of these elements. In combination with present surface water chemistry and chemical compositions of uraniferous minerals, the elevation of the analyzed elements in the recipient stream most likely arose from the liquid effluents, processing water, and acid drainage from the U mining/milling facilities. The dispersion of radionuclides and hazardous metals is actually limited to a small area at present, but some potential risk should not be negligible for local ecosystem. The results indicate that environmental remediation work is required to implement and future cleaner production technology should be oriented to avoid wide dispersion of radioactivity and non‐radioactive hazards in U mining/milling sites.  相似文献   

3.
We analyzed, U, Th and230Th/232Th activity ratios for a few tholeiites from the Mid-Atlantic Ridge FAMOUS zone at 36°50′N. The results show a fairly wide scatter for both Th/U and (230Th/232Th) ratios. Seawater contamination appears to be responsible for this scatter and, for the uranium, produces an increase in content yielding a (234U/238U) ratio greater than 1 and, for the Th, an increase of the (230Th/232Th) ratio which is a very sensitive indicator for contamination. Also, the latter often is selective: U, Th and Sr are not affected in the same manner.When discarding all data for contaminated samples, the FAMOUS zone appears to be very homogeneous with aTh/U ratio value of 3.05 and a (230Th/232Th) ratio value of 1.24. Comparison with other active volcanic areas reveals a negative correlation between (230Th/232Th) and87Sr/86Sr ratios for present lavas which is indicative of a consistency in Th-U and Rb-Sr fractionation in the source regions of these magmas. The Th isotopic geochemistry can thus provide useful information for the study of present volcanism, information as valuable as that from Sr, Pb or Nd isotopes.  相似文献   

4.
Natural concentrations of 238U and δ234U values were determined in estuarine surface waters and pore waters of the Amazon and Fly (Papua New Guinea) Rivers to investigate U transport phenomena across river-dominated land–sea margins. Discharge from large, tropical rivers is a major source of dissolved and solid materials transported to the oceans, and are important in defining not only oceanic mass budgets, but also terrestrial weathering rates.On the Amazon shelf, salinity-property plots of dissolved organic carbon, pH and total suspended matter revealed two vastly contrasting water masses that were energetically mixed. In this mixing zone, the distribution of uranium was highly non-conservative and exhibited extensive removal from the water column. Uranium removal was most pronounced within a salinity range of 0–16.6, and likely the result of scavenging and flocculation reactions with inorganic (i.e., Fe/Mn oxides) and organic colloids/particles. Removal of uranium may also be closely coupled to exchange and resuspension processes at the sediment/water interface. An inner-shelf pore water profile indicated the following diagenetic processes: extensive (1 m) zones of Fe(III)—and, to a lesser degree, Mn(IV)—reduction in the absence of significant S(II) concentrations appeared to facilitate the formation of various authigenic minerals (e.g., siderite, rhodocrosite and uraninite). The pore water dissolved 238U profile co-varied closely with Mn(II). Isotopic variations as evidenced in δ234U pore waters values from this site revealed information on the origin and history of particulate uranium. Only after a depth of about 1 m did the δ234U value approach unity (secular equilibrium), denoting a residual lattice bound uranium complex that is likely an upper-drainage basin weathering product. This suggests that the enriched δ234U values represent a riverine surface complexation product that is actively involved in Mn–Fe diagenetic cycles and surface complexation reactions.In the Fly River estuary, 238U appears to exhibit a reasonably conservative distribution as a function of salinity. The absence of observed U removal does not necessarily imply non-reactivity, but instead may record an integration of concurrent U removal and release processes. There is not a linear correlation between δ234U vs. 1/238U that would imply simple two component mixing. It is likely that resuspension of bottom sediments, prolonged residence times in the lower reaches of the Fly River, and energetic particle–colloid interactions contribute to the observed estuarine U distribution. The supply of uranium discharged from humid, tropical river systems to the sea appears to be foremost influenced by particle/water interactions that are ultimately governed by the particular physiographic and hydrologic characteristics of an estuary.  相似文献   

5.
A young (<1 m.y.) tholeiitic basalt dredged from the Mid-Atlantic Ridge displays a234U excess and a230Th deficiency that have resulted from the addition of seawater uranium during weathering at seafloor temperatures. Two older samples, though they acquired substantial amounts of uranium from seawater, are depleted in234U, indicating preferential leaching of this isotope. Hydrothermally altered samples suggest that some uranium loss may have occurred. Possible isotopic effects of preferential234U leaching, however, are obscured by secondary addition of seawater uranium at lower temperatures.  相似文献   

6.
The aim of this 6?year study was to assess whether freshwater inputs (rainfall and dam discharges) were acting as physical, physiological or trophic forcing factors on phytoplankton pigment concentrations and the dominant mysids of a temperate estuary (Guadalquivir estuary; SW, Spain). The effects of natural and human-controlled freshwater inputs modified the physico-chemical conditions and consequently biological production (bottom up control). Nutrient (nitrogen hypernutrification), suspended particulate matter and allochthonous photosynthetic pigment imports linked to freshwater inputs from adjacent habitats were observed, as well as light-limited autochthonous primary production. Seasonal and/or spatial patterns were shown by all study variables, including mysids. Freshwater management effects on dominant mysids differed depending on the species?? salinity tolerance (physiological forcing) and preferred prey availability (trophic forcing). Moreover, high inorganic matter content had a negative effect on the density of Mesopodopsis slabberi (physical forcing), which led to an increased detritivory/herbivory ratio (Neomysis integer/M. slabberi ratio). In conclusion, freshwater inputs appeared to effect estuarine lower trophic levels via a combination of different forcing mechanisms. Although several general patterns can be derived, the response of the system to freshwater inputs was not always univocal.  相似文献   

7.
Uranium and thorium isotope activities were measured by isotope dilution alpha spectrometry in four late Pleistocene and Holocene foraminiferal calcite samples. Sample cleaning methods were utilized to separate calcite tests from contaminating clay and surface oxide coatings. The maximum concentration of lattice bound uranium is 0.023 ppm (10 × 10?9 moles U/mole Ca), consistent with the lowest reported value, 0.025 ppm [1].230Th/234U activity ratios in samples cleaned as described above are much greater than one, indicating that the cleaning methods used do not effectively remove230Th from the surfaces of the calcite. The upper limit for lattice bound232Th is 0.039 ppm (17 × 10?9 moles Th/mole Ca).  相似文献   

8.
The aim of this study is to investigate the concentrations of U, Th, V, Mo, and Zr in natural waters taken from Turkey. Among these water species, Lake Van is the largest soda lake and the fourth largest closed basin on Earth. The water samples were collected from 51 locations between 2008 and 2009. The inductively coupled plasma‐MS was used for determinations. The obtained U and Zr concentrations are in the range of 37–110 µg L?1 and 17–78 µg L?1 in Lake Van and 0.53–0.81 µg L?1 and 0.15–0.19 µg L?1 in Lake Hazar, respectively. The concentration of uranium in other studied waters varies from the lowest 0.09 µg L?1 in Tigris (Dicle) river to the highest 4.0 µg L?1 in Mediterranean Sea water. Mean Mo and V concentrations in the studied water samples were found to be in ranges of 0.1–17 and 2.7–113 µg L?1, respectively. The obtained highest U concentration in Lake Van correlates with the highest Mo and Zr levels compared to the Lake Hazar and river waters. These results imply that there is a young occurrence of uranium minerals around Lake Van. It is concluded that there is about 50.000 ton of uranium in Lake Van water.  相似文献   

9.
Measurement of excess 234Th (t1/2 = 24.1 days) in surface sediment from 12 stations throughout Long Island Sound, U.S.A., demonstrates: (1) a mean (summer) sediment inventory of 3.6 dpm/cm2 consistent with complete, nearly instantaneous removal of 234Th from the overlying water and capture within the estuary, and (2) preferential association of excess 234Th with small particles and inventory build-ups in muddy bottom areas. There may also be a tendency for higher inventories in areas of high physical or biogenic reworking of surface sediments. A range of particle reworking rates (0–5 cm) from <0.01 × 10?6 to 1.6 × 10?6 cm2/s is found in the Sound with most values ～0.2?0.5 × 10?6 cm2/s. The inventory and reworking patterns demonstrate the high mobility, both horizontal and vertical, of particles in the estuary on 234Th decay time scales and are unequivocal evidence for control of reactive element distribution in the water column by the muddy regions of the basin.  相似文献   

10.
This study presents uranium and thorium concentrations and activity ratios for all riverine phases (bedload, suspended load, dissolved load and colloids) from basaltic terrains in Iceland and the Azores. Small basaltic islands, such as these, are thought to account for ~ 25% of CO2 consumed by global silicate weathering, and for ~ 45% of the flux of suspended material to the oceans. These data indicate that [U] and [Th] in the dissolved and colloidal fractions are strongly controlled by pH, and to a much lesser extent by levels of dissolved organic carbon (which are low in these environments). At high pH, basalt glass dissolution is enhanced, and secondary mineral formation (e.g. Fe-oxyhydroxides and allophane) is suppressed, resulting in high dissolved [U], and low colloidal [U] and [Th], indicating a direct chemical weathering control on elemental abundances. When the dissolved (234U/238U) activity ratio is >~1.3 (i.e. when physical weathering, groundwater contribution or soil formation are high), there is little isotope exchange between dissolved and colloidal fractions. At lower activity ratios, the dissolved load and colloids have indistinguishable activity ratios, suggesting that when chemical weathering rates are high, secondary clay formation is also high, and colloids rapidly adsorb dissolved U. Many of the suspended sediment samples have (234U/238U) activity ratios of > 1, which suggests that uptake of U onto the suspended load is important. Identical (230Th/232Th) in suspended, dissolved and colloidal samples suggests that Th, like U, is exchanged or sorbed rapidly between all riverine phases. This particle-reactivity, combined with poorly constrained contributions from groundwater and hydrothermal water, and short-term variations in input to soils (volcanic and glacial), suggests that U-series nuclides in riverine material from such basaltic terrains are unlikely to reflect steady state erosion processes.  相似文献   

11.
Two expeditions (October 1989 and May 1992) were carried out to two points of the main Amazon River channel and four tributaries. The Solimões and Madeira rivers, taking their origin in the Andes, are whitewater rivers. The Negro River is a typical acid, blackwater river. The Trombetas River flows through bauxite‐rich areas, and is characterized by low concentrations of dissolved humic substances. The 238U, 234U, 232Th and 230Th activities were recorded from dissolved, suspended particulate phases and river bank sediments. The latter were analysed for their 226Ra, 228Ra and 210Pb contents, and also subjected to leaching with 0·2 M hydroxylamine–hydrochloride solution to determine the concentrations of radionuclides bound to amorphous Fe hydroxides and Mn oxides and hydroxides. The dissolved U average concentration in the Amazon system is ten times lower than the mean world river concentration. The uranium concentration observed at Óbidos in the lower Amazon (0·095 µg L?1), where the U content in the river bank sediments and suspended matter is lowest, suggests U release from the solid phase during river transport. About 485 t of U are transported annually to the Amazon delta area in dissolved form, and 1943 t bound to suspended particulate matter. Total U and Th concentrations in the river bank sediments ranged from 1·59 to 7·14 µg g?1 and from 6·74 to 32 µg g?1, respectively. The highest concentrations were observed in the Trombetas River. The proportion extracted by means of the hydroxylamine solution (HL) was relatively high for U in the Trombetas river bank sediment (31%) and for Th in the Solimões sediment (30%). According to the alpha recoil effects, the 234U/238U activity ratios of the Andean river waters and downstream Amazon water (Óbidos) were >1, but were <1 in the Negro River (at Manaus). The activity ratios of dissolved U correlate with pH and also with the U activity ratios in the river bank sediment hydroxylamine extracts. As expected, the 234U/238U activity ratios in river bank sediments were <1 in the Andean rivers and in the downstream Amazon, but they were >1 in the Trombetas and Negro rivers. Such ratios probably result from the binding of dissolved uranium to solid sediment. The 228Th/232Th ratios of river bank sediments were close to unity (except for the Negro River, where it is lower), suggesting no significant Th exchanges between the river water and the sediment. The 226Ra/232Th activity ratios were <1, and the 226Ra/228Ra activity ratios generally were significantly higher than the activity ratios of their respective parents. This perhaps is the result of easier leaching of the 226Ra parent, 230Th, from solid material (owing to the alpha recoil effect) than of the 228Ra parent. Uranium and thorium isotopes were used as tools to evaluate the chemical weathering rate of rocks in the Amazon system, which was estimated to be 2·7 cm 1000 year?1 s?1. Copyright © 2002 John Wiley & Sons, Ltd.  相似文献   

12.
Spectral gamma ray wireline logging derives the concentrations of potassium, thorium, and uranium of the formation by measuring the gamma ray spectrum under the assumption of secular equilibrium. These measurements were carried out in a number of boreholes drilled by Ocean Drilling Program Leg 193 at the PACMANUS hydrothermal field. Spectral gamma ray logs from several of these holes show intervals of increased radioactivity, associated with high uranium values of up to 60 ppm (Snowcap hydrothermal field) and 25 ppm (Roman Ruins hydrothermal field). Nine samples of hydrothermally altered dacite were analyzed using gamma spectrometry to examine the origin of elevated radioactivity and to test for distortion of secular equilibrium. Core spectrometry indicates that secular equilibrium is distorted. Distortion can be explained by either an uptake of nuclides of the lower part of the 238U decay series, or by removal of 238U or 234Th from the rocks. In all cases wireline uranium logs and core spectrometry do not reflect true uranium concentrations of the formation but uranium is overestimated by a factor of 3–4. At Roman Ruins, uranium values from wireline logging show higher uranium concentrations over large intervals than uranium values from core spectrometry and from published core geochemistry, even when a possible leaching of uranium is taken into account. Wireline logs indicate that depth intervals of increased radioactivity are related to the occurrence of stockwork mineralization. In these depth intervals, core recovery was extremely low. In addition to the distortion of secular equilibrium, low core recovery and preferential loss of softer and more altered material cause a sampling bias between core samples and wireline data and may explain the observed difference in uranium concentrations between core and wireline logs.  相似文献   

13.
The geochronology of cave deposits in the Cradle of Humankind UNESCO World Heritage Site in South Africa provides a timeframe essential for the interpretation of its fossils. The uranium-lead (U–Pb) and uranium-thorium disequilibrium (U/Th) dating of speleothems, mostly flowstones that underlie and blanket the fossil-bearing sediments, have been effective in this sense, but U–Pb is limited by the requirement of ∼1 ppm U concentrations and low common Pb contents, and U/Th has a c. 500 ka limit of applicability. Here we report age results for calcite-aragonite speleothems obtained using a new combined uranium-thorium-helium ((U,Th)–He) and U/Th dating routine. We reproduced within analytical uncertainty, the published U–Pb or U/Th ages for (a) flowstone in three drill core samples in the range 2000–3000 ka, (b) a flowstone hand sample taken at surface with an age of 1800 ka, and (c) five underground flowstone samples in the range 100–800 ka. Calcite retentivity for He under cave conditions is thus demonstrated. In the few cases where helium loss was observed in speleothems, only some of the subsamples were affected, and to varying degrees, suggesting loss by lattice damage not related to diagenetic processes, rather than volume diffusion. In the 100 to 800 ka range, the combined U/Th disequilibrium and (U,Th)–He method also yielded reliable values for initial (230Th/238U) and (234U/238U) activity ratios. Importantly, most subsamples had high initial (230Th/238U) values, ranging from 1.0 to 19.7, although having low Th/U ratios. This is probably due to incorporation of Fe–Mn oxides-hydroxides dust, on which 230Th was previously adsorbed. Such samples are mostly not dateable by U/Th without the additional input from the He analysis. If not detected and corrected for, such high initial (230Th/238U) values can lead to inaccurate U/Th and U–Pb ages. Our study shows that the incorporation of He analysis in U/Th dating has broad potential application, with four methods for calculating the ages, in carbonates from different environments where U-Pb or U/Th dating would not work.  相似文献   

14.
Animal bones, associated with Palaeolithic artefacts and skeletal remains of early hominids from the cave of La Chaise-de-Vouthon, have been dated using a new approach to uranium series dating of bone. Speleothem (cave calcite) interstratified with bone-bearing sediments in the two chambers of Grotte Bourgeois-Delaunay and Grotte Suard have previously been dated by the 230Th/234 U method. This provides a chronological control for the bone ages, for which the method is still at an experimental stage. A good agreement is shown in most cases between the calcite and the bone ages, showing the cave to have been a stable environment for the deposition of bone and the acquisition of uranium.  相似文献   

15.
The activity concentrations of 226Ra and 228Ac in weathered Japanese soils from two selected prefectures have been measured using a γ-ray spectroscopy system with high purity germanium detector. The uranium, thorium, and rare earth elements (REEs) concentrations were determined from the same soil samples using inductively coupled plasma mass spectrometry (ICP-MS). For example, granitic rocks contain higher amounts of U, Th, and light REEs compared to other igneous rocks such as basalt and andesites. Therefore, it is necessary to understand the interaction between REEs and nature of soils since soils are complex heterogeneous mixture of organic and inorganic solids, water, and gases. In this paper, we will discuss about distribution pattern of 238U and 232Th along with REEs in soil samples of weathered acid rock (granite) collected from two prefectures of Japan: Hiroshima and Miyagi.  相似文献   

16.
The quantities of petroleum hydrocarbons being discharged to the Hudson Raritan estuary have been estimated, in tonnes day?1, from data in the literature as: sewage discharges (35), oil refinery discharges (1.3), non-oil refinery industrial discharges (17), oil spills (1.5), atmospheric deposition (0.002), urban and rural run-off (37). Losses have been estimated in a somewhat similar manner as: permanent deposition in sediments (11), dredging (5.8), advection (6.5), bed sedimentary transport (0.007), decomposition in water and sediments (42), evaporation (0.4), movement of surface slicks (0.4). The results are approximate but suggest that petroleum hydrocarbons originate principally from sewage as well as urban and rural run-off and only moderate proportions are discharged through the estuary mouth. However, this discharge combined with that due to dredging spoil disposal operations results in a considerable quantity of petroleum hydrocarbon entering the adjacent New York Bight.  相似文献   

17.
We analyzed uranium-series concentrations and isotopic ratios in a mixed aragonite and calcite stalagmite from Juxtlahuaca Cave, from the Sierra Madre del Sur of Mexico. The U-series data for the aragonite layers return highly precise and stratigraphically correct ages over the past ca. 4300 years. In contrast, age determinations from calcite layers are too old by several hundred years relative to the precise aragonite ages, have analytical uncertainties an order of magnitude larger than aragonite ages, and yield ages that do not overlap the aragonite ages within analytical uncertainties. Based on geochemical and petrographic observations, we interpret the calcite layers to have formed from recrystallization of aragonite soon after primary aragonite deposition. Calcite occurs as discontinuous lenses on and off the growth axis, and laminae can be traced between aragonite and calcite layers, demonstrating that visible growth banding is not effaced in the recrystallization process. Paired aragonite-calcite U-series data from coeval stratigraphic layers demonstrate that uranium concentrations decrease by two orders of magnitude during calcitization, and result in decreased (234U/238U). Uranium loss during diagenesis mimics a need for an age correction using an initial 230Th/232Th ratio one to two orders of magnitude larger than the bulk Earth ratio of 4.4 ± 2.2 × 10−6. A need for apparent high initial 230Th/232Th ratios results from ingrowth of 230Th during 234U decay.  相似文献   

18.
An iron-rich deposit dredged from the upper flank of Dellwood Seamount in the Northeast Pacific has been analyzed for major and trace elements, rare-earth contents and uranium isotopic composition. In terms of mineralogy and overall chemical composition, the deposit resembles other iron-rich deposits variously attributed to volcanic hydrothermal activity. Both the relative concentrations of the rare-earth elements and the isotopic composition of uranium rule out seawater as the sole source of elements in this deposit. The rare-earth element pattern indicates that these elements were derived from the underlying basalt. The234U/238U ratio is significantly higher than in seawater and can best be explained by preferential leaching of234U generated by decay from its parent238U in the underlying rock and subsequent redeposition of the excess234U together with the Fe and minor metals. These data are consistent with a model for the origin of submarine metal-rich solutions involving mobilization of elements from the interior of slowly cooling basalts by circulating seawater.  相似文献   

19.
Measurements of uranium concentration and the234U/238U activity ratio in oceanic basalts which have undergone low-temperature seafloor alteration indicate that uranium uptake is a pervasive occurrence but that the various phases involved behave differently with respect to this process. Palagonite exhibits uranium contents 8–20 times higher than unaltered glass coupled with low234U/238U, suggesting ongoing preferential leaching of234U. Altered crystalline interiors of several old basalts have234U/238U > 1, indicative of recent uranium exchange with seawater. The data also provide evidence for uranium sources with234U/238U higher than the seawater value of 1.14. Manganese crusts on basalts of a variety of ages have isotopic ratios indicating that they either are recent deposits or also have experienced continuing uranium exchange with seawater.  相似文献   

20.
Zafarraya Cave is considered a reference site for the last presence of Homo neanderthalensis presence in the south of the Iberian Peninsula. In this paper, accelerator mass spectrometry (AMS) radiocarbon dates were carried out on charcoals and faunal remains, U–Th dating using either alpha spectrometry or Thermal-Ionization Mass Spectrometry (TIMS) and ESR dating were performed on faunal remains. These analyses were carried out on samples from the Mousterian levels of the site (archaeostratigraphic units UC, UD, UE, UF, UG). The 14C AMS dates of charcoal samples (n = 11) were scattered and displayed no coherence with the stratigraphy suggesting possible alteration. The delicate charcoal and faunal samples underwent the gentle RR, ZR (ABA) or AG (ABA) pretreatment procedures at ORAU. The RR protocol is currently considered too gentle and the results are considered with caution. Four ZR charcoal pretreatments failed due to the fact that the charcoal samples were altered. Only two charcoals samples subjected to the ZR pretreatment yielded a reliable % C (>60%) (OxA-9001 and OxA-9002, 40,294–42,761 and 38,763–40,604 cal BP). Their ages are consistent with the stratigraphy and are considered to provide the best age estimate for the level bearing the Z2 Neandertal mandible (Unit UE). For the dentine and the bone samples, the 14C AMS were less dispersed. 14C analyses failed for four bone samples due to insufficient collagen content. Moreover, the %C is very low for two samples, suggesting alteration of the fossil remains at Zafarraya. Only two other samples with enough %C (>30%) were retained: OxA-8024 and OxA-8999 (Unit UE). The respective 14C ages range from ∼34 to 39 ka cal BP. The U/Th (TIMS) analyses of enamel samples displayed an extremely low uranium content (< ∼ 0.02–0.04 ppm). Moreover, the U/Th age range of faunal remains is large, thus providing no conclusive results. ESR dating was chosen for this exercise as, in combination with U-series, it can be used to assess U-uptake in open systems. The combined ESR and U/Th (TIMS) age estimates on tooth enamel yielded US-ESR ages between 33 (+3/−4) ka to 43 ± 3 ka (MIS3) for two Equus teeth and one Capra tooth in unit UE, overlapping with the oldest charcoal and bone 14C dates. The age of the Zafarraya fossil remains was derived from the US-ESR time range of 30–46 ka (MIS 3). We consider this age range to be more representative of the Neandertal occupations at the site than the hitherto widely cited uncalibrated 14C age of around 30 ka.  相似文献   

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