Temporal evolution of lead isotope ratios in sediments of the Central Portuguese Margin: A fingerprint of human activities

Stable Pb isotope ratios (²⁰⁶Pb/²⁰⁷Pb, ²⁰⁸Pb/²⁰⁶Pb), ²¹⁰Pb, Pb, Al, Ca, Fe, Mn and Si concentrations were measured in 7 sediment cores from the west coast of the Iberian Peninsula to assess the Pb contamination throughout the last 200 years. Independently of their locations, all cores are characterized by increasing Pb/Al rends not related to grain-size changes. Conversely, decreasing trends of ²⁰⁶Pb/²⁰⁷Pb were found towards the present. This tendency suggest a change in Pb sources reflecting an increased proportion derived from anthropogenic activities. The highest anthropogenic Pb inventories for sediments younger than 1950s were found in the two shallowest cores of Cascais and Lisboa submarine canyons, reflecting the proximity of the Tagus estuary. Lead isotope signatures also help demonstrate that sediments contaminated with Pb are not constrained to estuarine–coastal areas and upper parts of submarine canyons, but are also to transferred to a lesser extent to deeper parts of the Portuguese Margin.     

Characterization of lake water and ground water movement in the littoral zone of Williams Lake,a closed‐basin lake in north central Minnesota

Williams Lake, Minnesota is a closed‐basin lake that is a flow‐through system with respect to ground water. Ground‐water input represents half of the annual water input and most of the chemical input to the lake. Chemical budgets indicate that the lake is a sink for calcium, yet surficial sediments contain little calcium carbonate. Sediment pore‐water samplers (peepers) were used to characterize solute fluxes at the lake‐water–ground‐water interface in the littoral zone and resolve the apparent disparity between the chemical budget and sediment data. Pore‐water depth profiles of the stable isotopes δ¹⁸O and δ²H were non‐linear where ground water seeped into the lake, with a sharp transition from lake‐water values to ground‐water values in the top 10 cm of sediment. These data indicate that advective inflow to the lake is the primary mechanism for solute flux from ground water. Linear interstitial velocities determined from δ²H profiles (316 to 528 cm/yr) were consistent with velocities determined independently from water budget data and sediment porosity (366 cm/yr). Stable isotope profiles were generally linear where water flowed out of the lake into ground water. However, calcium profiles were not linear in the same area and varied in response to input of calcium carbonate from the littoral zone and subsequent dissolution. The comparison of pore‐water calcium profiles to pore‐water stable isotope profiles indicate calcium is not conservative. Based on the previous understanding that 40–50 % of the calcium in Williams Lake is retained, the pore‐water profiles indicate aquatic plants in the littoral zone are recycling the retained portion of calcium. The difference between the pore‐water depth profiles of calcium and δ¹⁸O and δ²H demonstrate the importance of using stable isotopes to evaluate flow direction and source through the lake‐water–ground‐water interface and evaluate mechanisms controlling the chemical balance of lakes. Published in 2003 by John Wiley & Sons, Ltd.     

Historical record of metal accumulation and lead source in the southeastern coastal region of Korea

Concentrations of heavy metals and Pb isotopes were measured in the 1-M HCl leaching fraction of core sediments spanning the last 400 years. This sedimentary record of pollution history in metal concentrations shows a good correlation with the increases in industrialization, urbanization, and energy consumption since 1901s. Notably, the Pb concentration and the ²⁰⁷Pb/²⁰⁶Pb and ²⁰⁸Pb/²⁰⁶Pb ratios were constant before the 1910s (16.7 μg/g, 0.844, and 2.098, respectively), whereas they increased steadily up to 21.9 μg/g, 0.848, and 2.101 after the 1910s. The correlations between Pb isotope ratios (²⁰⁶Pb, ²⁰⁷Pb, and ²⁰⁸Pb) showed different linear regression trends for core sediments before and after the 1910s, indicating differences in Pb sources. Our interpretation suggests that the source of anthropogenic Pb in Korean coastal region and the Yellow Sea shelf was presumed to be Chinese coals or ores, which have also played a major role as sources of atmospheric particulate Pb.     

137Cs湖泊沉积年代学方法应用的局限——以Crawford湖为例

＾１３７Ｃｓ湖泊沉积年代学方法是测定现代湖泊沉积物沉积年代和沉积速率的重要同位素年代学方法之一。对加拿大Ｃｒａｗｆｏｒｄ湖采集的沉积孔柱内＾１３７Ｃｓ垂直分布的研究发现,该方法给出时的标有明显偏差。比较＾２１０Ｐｂ和纹层等年代方法的结果,其１９６３年时标蓄积峰值所在位置明显移向表层,而作为１９５４年时标的该核素出现蓄积的层位则远早于该年沉积物蓄积层位。研究还表明,孔柱中较高的间隙水含量、缺少足以吸     

Source area and seasonal 87Sr/86Sr variations in rivers of the Amazon basin

We report the results of a detailed study of dissolved Sr isotopes in the Solimões and Beni‐Madeira Rivers of the Amazon basin. This study developed data collected over 8 years indicating large spatial and temporal variations in dissolved Sr isotopes among the rivers of the Amazon basin. The large ⁸⁷Sr/⁸⁶Sr variations were found to be correlated with the geology of the source areas of the suspended sediments. The Beni‐Madeira River displays a high average ⁸⁷Sr/⁸⁶Sr ratio and large ⁸⁷Sr/⁸⁶Sr fluctuations during the hydrological cycle. This large average value and fluctuations were related to the presence of Precambrian rocks and Ordovician sediments in the source area of the suspended sediment of the river. In contrast, the Solimões River displays a narrow range of Sr isotope ratio variations and an average value close to 0.709. This river drains mostly Phanerozoic rocks of northern Peru and Ecuador that are characterized by low Sr isotope ratios. The isotopic fluctuations in the Beni‐Madeira River were observed to propagate downstream at least as far as Óbidos. This signal is characterized by an inverse relationship between the concentration of elemental Sr and its isotopic ratios. We further demonstrate that the Sr isotopic composition and content in the Beni‐Madeira River is controlled by suspended sediments derived from the Andes. Despite draining areas underlain by Precambrian rocks and having high ⁸⁷Sr/⁸⁶Sr ratios, such rivers as the Negro and Tapajós play a minor role in the total Sr budget of the Amazon basin. Copyright © 2013 John Wiley & Sons, Ltd.     

Dating of sediments from Lake Zurich (Switzerland) with210Pb and137Cs

²¹⁰Pb- and¹³⁷Cs-measurements, and varve counting have been used to date sediment cores from Lake Zurich (Switzerland). Two cores from different water depths were dated with²¹⁰Pb/²¹⁰Po and revealed sediment accumulation rates of (0.055±0.015) g·cm^?2·y^?1 and (0.09±0.03) g·cm^?2·y^?1, respectively. A comparable rate of (0.07±0.01) g·cm^?2·y^?1 has been obtained from¹³⁷Cs measurements. These rates were confirmed by annual layer (varve)-counts which lead to rates of 0.07 g·cm^?2·y^?1. Constant²¹⁰Pb activities were observed in the top 6 cm of the sediment cores. This constancy is generally explained in the literature by mixing processes caused by bioturbation and by distortion during coring operations of the uppermost water-rich fluffy sediments. However the distinct¹³⁷Cs-maxima and the regular and undisturbed varve lamination of the top sediment observed in the cores of Lake Zurich contradict this assumption. In addition, measurements of⁷Be at the water/sediment interaces proved complete sediment core recovery and mechanically undisturbed sediments. Remobilization processes are assumed to cause the observed constant²¹⁰Pb activities. Remobilization may also be the reason for an incomplete²¹⁰Pb inventory in the sediments which contain only about 50% of the fallout from atmosphere. The results of the²¹⁰Pb dating should therefore be considered with some care. If existent, varve counting represents the easiest and most reliable means for dating lake sediments.     

Chemical forms of Pb, Zn and Cu in the sediment profiles of the Pearl River Estuary

The chemical forms of heavy metals (Pb, Zn and Cu) in sediment cores of the Pearl River Estuary were studied using a sequential chemical extraction method. The isotope ratios of 206Pb/207Pb in various chemical fractions were also measured to assess the potential Pb sources. Zinc and Cu were mainly associated with the residual fraction. The Fe-Mn oxide and organic/sulphide fractions were the next important phases for Zn and Cu, respectively. For Pb, different chemical partitioning patterns were found among different sediment cores. Most Pb was associated with the residual fraction in the sediments. In some sediment profiles, the major phase of Pb in the top layers was the Fe-Mn oxide fraction. The proportion of Pb in the Fe-Mn oxide fraction decreased significantly with increasing depth. Among the different depths, the 206Pb/207Pb isotope ratios in the residual fraction remained fairly stable, with a mean value of 1.202, which may represent the natural background value. The 206Pb/207Pb ratios in the exchangeable fraction were the lowest among the five fractions, particularly in top sediments, showing the anthropogenic inputs of heavy metals from recent rapid industrial development in the surrounding region. For the other three non-residual fractions, there was a similar trend of increasing 206Pb/207Pb ratios down the profile. Results from this study are useful in assessing both the chemical changes for heavy metals in marine sediments and the potential of heavy metal release into the water environment of an estuary area.     

A multi-isotopic and trace element investigation of the Cretaceous-Tertiary boundary layer at Stevns Klint, Denmark - inferences for the origin and nature of siderophile and lithophile element geochemical anomalies

Os, Sr, Nd and Pb isotope data were collected from a profile across the Cretaceous-Tertiary (K-T) boundary layer at Stevns Klint, Denmark. ?_Nd [T=65 Ma] values from within the boundary layer (Fish Clay) are lower by ∼1 ? unit than those of the underlying Maastrichtian limestone and the overlying Danian chalk sequences. Systematic profile-upward changes of Pb, Sr and Os isotopic compositions and concentrations in the boundary layer cannot be accounted for by in situ growth of daughter products since the sedimentation of the Fish Clay. While Os, Nd and Pb isotopes indicate the admixing of less radiogenic components to the Fish Clay, Sr isotopes show elevated radiogenic values in the boundary layer, relative to the carbonate sequences beneath and above it. The sudden change in lithophile (e.g., Sr, Pb and Nd) isotope compositions at the base of the Fish Clay and profile-upward trends of ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb ratios towards those of the overlying Danian chalk are interpreted to reflect recovery from enhanced, acid rain-induced continental (local?) weathering input to the seawater. However, a continental crustal source is invalid for the siderophile element Os. In the light of evidence from chromium isotopes for a cosmic origin of the platinum group elements (PGEs) and certain moderately siderophile elements (Cr, Ni, Co, V) in K-T boundary sediments, including Stevns Klint [Shukolyukov and Lugmair, Science 282 (1998) 927-929], and supported by the finding of projectile debris [Bauluz et al., Earth Planet. Sci. Lett. 182 (2000) 127-136] and the occurrence of abundant Ni-rich spinel at many K-T sites [Robin et al., Nature 363 (1993) 615-617; Kyte, Nature 396 (1998) 237-239], we favor to explain the sudden drop of ¹⁸⁷Os/¹⁸⁸Os ratios from 0.210 to 0.160 at the K-T boundary to derive from global fall-out of extraterrestrial matter. The present ¹⁸⁶Os/¹⁸⁸Os ratio of 0.119836±0.000004 measured in the basal layer of the Fish Clay is within the uncertainty a chondritic value. We therefore exclude the possibility of a major contribution of PGEs to the sediment from iron meteorites. Chondrite-normalized (Ru/Ir)_N ratios of ∼0.95±0.14 and (Os/Ir)_N ratios of ∼0.93±0.14 in the Fish Clay cannot distinguish between abundance ratios of different types of chondrites, and strongly sub-chondritic (Pt/Ir)_N ratios of ∼0.62±0.09 (2σ) suggest differential PGE remobilization through the sedimentary column (and consequently the alteration of inter-element ratios). PGEs and the moderately siderophile elements Cr, Ni, V, and Co form an elemental association with systematically upward-decreasing concentrations in the Fish Clay. Low Co/Ni ratios of ∼0.12 in the Fish Clay relative to values of ∼0.35 in the over- and underlying carbonate sequences support mixing of meteorite-derived (Co/Ni ∼0.05) and terrestrial upper mantle/crustal (Co/Ni >∼0.3) sources. While lithophile element isotope data indicate an increased continental crustal input to the Fish Clay at the K-T transition, the uncertainty with respect to possible post-depositional alteration of abundance patterns of siderophile and moderately siderophile elements - though not affecting the chondritic isotopic composition of Os - does not allow confirmation of indications from chromium isotopes for a carbonaceous (CV-type) meteorite as the preferred K-T impactor type by Shukolyukov and Lugmair [Science 282 (1998) 927-929].     

Quantitative reconstruction of the lake water paleotemperature of Daihai Lake, Inner Mongolia, China and its significance in paleoclimate

By measuring Sr/Ca ratios of the ostracod shells (Limnocthere cf. inopinata) in sediments of the Daihai Lake, and combined with Sr²⁺/Ca²⁺ ratios of the lake water, this paper obtained paleosalinity of the lake water. Vaporizing experiment of the lake water in laboratory showed that there was a quantitative relationship between salinity and oxygen isotope. Using this relationship, oxygen isotope values of the paleo-lake water were calculated. By measuring the oxygen isotope of the authigenic carbonate in the lake’s sediments, and in combination with the oxygen isotope values of the paleo-lake water, the paleotemperature of the lake water was calculated. Finally, based on these proxies, the paleoclimate in the lake basin was explored.     

Source and distribution of lead in the surface sediments from the South China Sea as derived from Pb isotopes

Rapid economic development in East Asian countries has inevitably resulted in environmental degradation in the surrounding seas, and concern for the environment and its protection against pollutants is increasing. Identification of sources of contaminants and evaluation of current environmental status are essential to environmental pollution management, but relatively little has been done in the South China Sea (SCS). In order to investigate the abundance, distribution, and sources of Pb within the SCS, stable Pb isotopes and their ratios were employed to assess the contamination status and to differentiate between natural and anthropogenic origins of Pb in the surface sediments. The total Pb concentrations in sediments varied from 4.18 to 58.7 mg kg⁻¹, with an average concentration of 23.6 ± 8.9 mg kg⁻¹. The observed Pb isotope ratios varied from 18.039 to 19.211 for ²⁰⁶Pb/²⁰⁴Pb, 15.228 to 16.080 for ²⁰⁷Pb/²⁰⁴Pb, 37.786 to 39.951 for ²⁰⁸Pb/²⁰⁴Pb, 1.176 to 1.235 for ²⁰⁶Pb/²⁰⁷Pb, and 2.468 to 2.521 for ²⁰⁸Pb/²⁰⁷Pb. The majority of these ratios are similar to those reported for natural detrital materials. Combined with Pb enrichment factor values, our results show that Pb found within most of the SCS sediments was mainly derived from natural sources, and that there was not significant Pb pollution from anthropogenic sources before 1998. Further studies are needed to reconstruct deposition history and for trend analysis.     

Lead and strontium isotopes in Cretaceous kimberlites and mantle-derived xenoliths from Southern Africa

Concentrations of lead, uranium and thorium and isotopic compositions of lead are reported for twelve Cretaceous kimberlites and five Cretaceous nucleated autoliths. The samples are from Lesotho and from the area around Kimberley (Cape Province, South Africa). In the case of the autoliths potassium, rubidium and strontium concentrations and⁸⁷Sr/⁸⁶Sr ratios were also measured.Work reported on clinopyroxenes from mantle-derived xenoliths in kimberlites includes lead isotopes for twelve samples and strontium isotopes for nine of these.The autoliths have initial⁸⁷Sr/⁸⁶Sr ratios between 0.7035 and 0.7095. A large spread in initial lead isotope ratios (²⁰⁶Pb/²⁰⁴Pb: 17.6–20;²⁰⁸Pb/²⁰⁴Pb: 37.7–39.5) was found in the matrix kimberlites and autoliths. In the²⁰⁷Pb/²⁰⁴Pb vs.²⁰⁶Pb/²⁰⁴Pb plot, the initial lead isotope ratios of the kimberlite and autolith samples roughly define a slope of 0.10, corresponding to an age of 1575 m.y. With respect to the spread of initial ratios as well as with respect to this slope, the kimberlite and autolith lead isotopic pattern is comparable to patterns obtained from carbonatites and ocean island volcanics.The xenoliths studied include coarse-granular and porphyroclastic material from the Kimberley area and coarse-granular samples from Lesotho. Their⁸⁷Sr/⁸⁶Sr ratios are generally between 0.704 and 0.706 but a value of 0.713 was found in one sample. They show a surprisingly large spread in lead isotope ratios (²⁰⁶Pb/²⁰⁴Pb: 17.5–20;²⁰⁸Pb/²⁰⁴Pb: 37.3–39.4).The isotopic patterns of the xenolithic material and of the kimberlites and autoliths are considered to provide a strong indication that the upper mantle beneath Southern Africa is isotopically heterogeneous on a regional scale.     

Isotopic composition of lead and strontium in lavas and coarse-grained blocks from Ascension Island,South Atlantic

New Sr and Pb isotope data are presented for a selection of lavas and associated coarse-grained blocks from Ascension Island. K-Ar dates for the lavas range up to1.5±0.2Ma. Initial⁸⁷Sr/⁸⁶Sr ratios are consistent with earlier measurements and for most rocks are ca. 0.7029, but range up to 0.7135 in the case of the most evolved lavas and blocks. Pb isotope data are also consistent with earlier measurements, but the Pb in two gabbroic blocks is less radiogenic than Pb in the other rocks. It is suggested that these gabbroic blocks crystallized from a magma of tholeiitic composition whose source was similar to that of mid-oceanic ridge basalt whereas the lavas and other blocks crystallized from mildly alkaline magmas derived from a source further from the crest of the Mid-Atlantic Ridge. The high⁸⁷Sr/⁸⁶Sr ratios result from contamination of the most silicic magma by radiogenic Sr from pelagic sediments. These data and their interpretation are consistent with the petrological and geochemical observations that the granite blocks are the coarse-grained equivalents of the volcanic suite [11] and not fragments of relict continental material [2,3].     

Fluxes of uranium and thorium series isotopes in the Santa Barbara Basin

Samples from the MANOP Santa Barbara Basin sediment trap intercomparison were analyzed for the isotopes of uranium, thorium, radium, lead, and polonium. All of the traps showed approximately the same compositions and isotopic ratios, indicating that they trapped similar materials. The²³⁴Th flux via falling particles was very close to the flux predicted from the production and scavenging rates of²³⁴Th from the water column. The²¹⁰Pb content of the trapped particles and the surface sediments were the same, however, the measured flux of²¹⁰Pb was seven times greater than the predicted flux. Predicted and measured fluxes of²²⁸Th and²¹⁰Po were similarly out of balance. To explain this apparent inconsistency, we suggest (as others have done) that the Santa Barbara Basin is an area where scavenging from the water column is intensified and where sediments deposited initially on the margins may be physically remobilized on a short time scale. These two effects increase the apparent area from which the basin derives the longer-lived isotopes but does not increase significantly the supply of the short-lived²³⁴Th.     

Ce anomalies in Gough Island lavas — Trace element characteristics of a recycled sediment component

High precision trace element data obtained by inductively coupled plasma mass spectrometry and Sr–Nd isotope analyses are presented for mafic volcanic rocks from Gough Island, South Atlantic. The new data reveal negative Ce anomalies, with Ce/Ce^? values in Gough lavas extending down to ～ 0.92. Ce is only fractionated from other rare earth elements (REE) due to formation of Ce⁴⁺ under oxidizing conditions of near-surface environments while other REE remain trivalent. Ce anomalies in convergent margin magmas have been shown to indicate a contribution of a subducted sediment component. In contrast, Ce anomalies in intra-plate basalts have been attributed to weathering processes, but can be excluded here based on element–element systematics indicating magmatic trends rather than weathering-induced element mobility. Shallow-level contamination by local marine sediments with negative Ce anomaly inherited from seawater can be excluded because Gough lavas with increasingly negative Ce anomalies do not trend towards low Ce/Pb ratios characterizing such sediments. Rather, it is argued that the negative Ce anomalies in Gough Island lavas are consistent with variable amounts of a sediment component in the mantle plume source. Mixtures between estimates of subducting sediment columns with negative Ce anomaly and mantle capable of giving rise to Gough Island magmas without Ce anomalies reproduce the Gough compositional array with the exception of highly fluid-mobile elements. The calculated trace element composition of the deeply recycled sediment in the Gough plume source is depleted in fluid-mobile elements such as Ba and Pb relative to the composition of some present-day subducting sediments. This loss is attributed to the dehydration or flushing of sediment in the subduction factory, consistent with constraints from arc magmas.     

Dual effects of precipitation and evaporation on lake water stable isotope composition in the monsoon region

We present the results of a 3‐year monitoring programme of the stable isotope composition of lake water and precipitation at Taozi Lake, in the East Asian monsoon region of China. Our aims were to reveal the spatiotemporal pattern of variation of stable isotopes in a small closed‐basin lake and to quantitatively determine the impacts of precipitation and evaporation on the stable isotope composition of lake water under a humid monsoon climate. In the time domain, the stable oxygen isotopic ratio of the lake water (δ¹⁸O_L) exhibited substantial seasonal and interannual variations, but the isotope variations between different precipitation events substantially exceeded seasonal and interannual variations. Compared with the stable isotopes in precipitation, δ¹⁸O_L was substantially positive and d_L was negative. In the space domains, the lake water was homogeneously mixed. Indicated by statistic analyses, precipitation plays a dominant role in dynamic of the lake stable isotope during precipitation events of relatively large magnitude, whereas the effect of evaporation is dominant during smaller precipitation events. Results advance our understanding of the stable isotope change rule in the process of lake water evaporation, and it is helpful to identify the climatic significance recorded in stable isotopic compositions of lake bottom sediments.     

Stable Pb isotope ratios in aerosols, precipitation, and size-fractionated particulate matter in the Gulf of Maine, Scotian Shelf, and Labrador Sea

Measurements of Pb isotopes in aerosols, precipitation, and size-fractionated particulate matter from the Gulf of Maine, Scotian Shelf and Labrador Sea are used to investigate the source of Pb. The ²⁰⁶Pb/²⁰⁷Pb ratio in aerosols and precipitation collected at New Castle, NH suggests that anthropogenic Pb is a mixture of US and Canadian sources. ²⁰⁶Pb/²⁰⁷Pb ratios in >53 μm particulate matter from the Gulf of Maine and Scotian Shelf slope waters are consistent with contaminant Pb inputs predominantly from US and Canadian sources, while in shelf waters ²⁰⁶Pb/²⁰⁷Pb ratios in >0.4 μm and >53 μm particles are consistent with a mixture of US and Canadian sources, as well as Pb associated with resuspended surface sediment. ²⁰⁶Pb/²⁰⁷Pb ratios in particulate matter (>0.4 μm, 10-53 μm, and >53 μm) from Labrador Sea surface waters range from 1.165 to 1.211 and are a mixture of Pb derived from ore compositions consistent with Broken Hill, Australia and southeast Missouri, US sources.     

Pb‐isotope compositions of the Tasik Chini volcanic‐hosted massive sulfide deposit,Central Belt of Peninsular Malaysia: Implication for source region and tectonic setting

Lead isotope data of sulfides and host volcanic rocks from the Bukit Botol and Bukit Ketaya deposits, the two representative deposits of the Tasik Chini volcanic‐hosted massive sulfide (VHMS) deposit, Central Belt of Peninsular Malaysia, are reported. Lead isotope compositions of the associated sulfide minerals and volcanic rocks from the Bukit Botol deposit exhibit homogeneous and less radiogenic values (²⁰⁶Pb/²⁰⁴Pb showing a range of composition from 18.14 to 18.20, ²⁰⁷Pb/²⁰⁴Pb between 15.52 and 15.59 and ²⁰⁸Pb/²⁰⁴Pb from 37.96 to 38.35). Similarly, the Pb isotopic compositions of the host volcanic rocks from the Bukit Ketaya deposit yielded a narrow range to those of the sulfide samples (²⁰⁶Pb/²⁰⁴Pb from 18.04 to 18.20, ²⁰⁷Pb/²⁰⁴Pb between 15.43 and 15.57 and ²⁰⁸Pb/²⁰⁴Pb of 37.96 to 38.30). The uniform Pb‐isotope compositions of the sulfides in the ore horizon and the host volcanic rocks from both deposits suggest a derivation from a similar source reservoir and mineralization processes. In the framework of the tectonic model for the Central Belt of Peninsular Malaysia, both deposits display a range of lead isotopic compositions originated from mixing of bulk crust/juvenile arc and minor mantle sources, which are typical for VHMS deposits in an island arc–back arc setting.     

Lithium isotope variations in Tonga–Kermadec arc–Lau back‐arc lavas and Deep Sea Drilling Project (DSDP) Site 204 sediments

Lithium isotopes have been identified as a promising tracer of subducted materials in arc lavas due to the observable variations in related reservoirs such as subducting sediments and altered oceanic crust. The Tonga–Kermadec arc–Lau back‐arc provides an end‐member of subduction zones with the coldest thermal structure on Earth. Reported here are Li isotope data for 14 lavas from the arc front and 7 back‐arc lavas as well as 12 pelagic and volcaniclastic sediments along a profile through the sedimentary sequence at DSDP Site 204. The arc and back‐arc lavas range from basalts to dacites in composition with SiO₂ = 48.3–65.3 wt% over which Li concentrations increase from 2 ppm to 16 ppm. Li/Y ratios range from 0.08 to 0.77 and from 0.24 to 0.65 in the arc and back‐arc lavas, respectively. The majority of the lavas have δ⁷Li that ranges from 2.5 ‰ to 5.0 ‰ with an average of (3.6 ±0.7) ‰, similar to that reported from other arcs and there is no distinction between the arc front and back‐arc lavas. The pelagic sediments have variable Li concentrations (33–133 ppm) and δ⁷Li that ranges from 1.2 ‰ to 10.2 ‰ while the volcaniclastic sediments have an even greater range of Li concentrations (3.6–165 ppm) and generally higher δ⁷Li values (8–14 ‰). However, δ⁷Li in the lavas does not correlate with commonly used trace element ratio or isotope signatures indicative of slab‐derived fluids or the sediments. This is probably because the range of δ⁷Li in the lavas and sediments overlap. Calculated sediment mass‐balance models require significantly more sediment than previous estimates based on Th–Nd–Be isotopes. This may indicate that a sizeable proportion of the total Li budget in the lavas is provided by Li‐enriched fluids from the subducting sediments and/or altered oceanic crust.     

210pb as a chronometer and tracer,Burrinjuck Reservoir,Australia

Cores taken at Burrinjuck Reservoir in southeastern New South Wales have been dated using the first appearance of ¹³⁷Cs, charcoal/bushfire correlations, and annual grass pollen peaks. None of the main ²¹⁰Pb dating models reproduced the ‘known’ chronology. Correlation analysis shows no significant relationship between original ²¹⁰Pb (unsupp.) concentration and grain-size, sedimentation rate or loss on ignition. Differences in sediment source may explain the variations in ²¹⁰Pb. A simple provenance model has been used to interpret the ratio of original ²¹⁰Pb (unsupp.)/²²⁶Ra as a tracer of topsoils and subsoils. High ratios in the reservoir sediments probably indicate eroded topsoils and low ratios eroded subsoils.     

Sediment yields and sources in a welsh upland lake-catchment during the past 800 years

Estimates of suspended sediment yield over the past 800 years have been derived from a whole-basin study of lake sediments in Llyn Geirionydd, North Wales. Magnetic and physical sediment properties were used to correlate a suite of cores to a master chronology based on ²¹⁰Pb and ¹⁴C dates. The sources of sediment within the catchment were identified by comparing the magnetic and heavy metal properties of sediments, soils, and stream sediments. Mean suspended sediment yields range from 6 to 18 t km^?2 yr^?1 with high yields in the periods 1765-1830 and 1903-1985 corresponding to mining activities in the catchment. The impact of earlier deforestation, agricultural expansion, or climatic change on sediment yields is low, although there is evidence that agricultural activities increased levels of peak stream discharge. Afforestation in the 20th century does not appear to have significantly increased sediment yield. Sediment sources have remained fairly constant through time; they appear to be widespread and dominated by stream channel sides rather than point sources, except during the mining phases when spoil material has dominated the sediment load. Sediment loads to the lake today are still dominated by sediment derived from unvegetated spoil heaps.