Palaeohydrological significance of late Quaternary strontium isotope ratios in a tropical lake

Ostracods preserved in late Quaternary sediments of Wallywash Great Pond, a fresh coastal lake in SW Jamaica, record temporal variations in the strontium-isotope composition of lake water. Oxygen-isotope and Sr/Ca ratios in ostracods reveal temporal variations in the lake's hydrology, related to effective precipitation, and in its salinity related to varying marine-saline groundwater input from changes in relative sea level. Evaluation of isotopic and trace-element data indicates that the stratigraphic variations in ⁸⁷Sr/⁸⁶Sr ratios during the late Quaternary are best explained by climatically-controlled hydrological changes. During wetter periods, the lake's Sr budget was dominated by springwater input with relatively low ⁸⁷Sr/⁸⁶Sr ratio, whereas during drier times reduced springflow, possibly coupled with input of more-radiogenic Sr from other sources, such as sea-spray aerosols and perhaps Saharan dust, led to an increase in the Sr-isotope ratio of the lake water. Despite proximity of the lake to the sea and evidence for slight intrusion of marine saline groundwater in the past, however, the extent of marine input appears to have had limited influence on the lake's Sr-isotope ratios. Whereas the ⁸⁷Sr/⁸⁶Sr ratios cannot be used as a palaeosalinity proxy in this particular lake, they do provide valuable information about the mechanisms underlying hydrological change.     

Sr/Sr and Sr/Ca in speleothems for paleoclimate reconstruction in Central China between 70 and 280 kyr ago

Limestone cave deposits (speleothems) provide archives for past changes in regional climates over a range of timescales. While δ¹⁸O and δ¹³C in speleothem calcite have been commonly used for reconstruction of paleoclimates, we report here further efforts in the use of ⁸⁷Sr/⁸⁶Sr and Sr/Ca signals in speleothem calcite to deduce paleomonsoon variability near the Loess Plateau of central China. A two end-member mass-balance model of concentration and isotopic composition of strontium in a cave system is used to estimate variation of the ⁸⁷Sr/⁸⁶Sr ratio in sediments overlying a limestone cave. We show that this ratio reflects climate-driven variations in the provenance and the extent of chemical weathering of the epikarstic sediments. The measurements of ⁸⁷Sr/⁸⁶Sr made on a well-dated stalagmite, SFL, from Buddha Cave (33^o40N′ 109^o05′E) show ratios of 0.71092 to 0.71133 (±0.00001 as 2σ) during relatively cold periods (e.g., Marine Isotope Stage (MIS) 5b, 5d, and 8), lower than ratios of 0.71133 to 0.71194 during relatively warm periods (e.g., MIS 5a, 5c, 5e, and 7). As changes in the Sr/Ca ratio may affect speleothem ⁸⁷Sr/⁸⁶Sr, we show that the direct use of speleothem ⁸⁷Sr/⁸⁶Sr is less ideal than our modeled ⁸⁷Sr/⁸⁶Sr for the exogenic Sr source above the cave as a paleomonsoon proxy. Using the δ¹⁸O, δ¹³C, Sr/Ca, and ⁸⁷Sr/⁸⁶Sr records of the stalagmite, we reconstruct the variability of the East Asian monsoon for the time period between 70 and 280 kyr ago. The results show that summer monsoons were more intense during interglacial periods than during glacial periods.     

Strontium-isotope studies of “brown water” (organic-rich groundwater) from Denmark

 Groundwater from some Quaternary and upper Tertiary aquifers in western Jutland, Denmark, is heavily influenced by "brown water", i.e., groundwater with a high content of naturally occurring dissolved organic matter. Stable-isotope analyses (¹⁸O/¹⁶O and D/H) indicate that both Quaternary and upper Tertiary aquifers are dominated by meteoric water. However, strontium-isotope analyses make it possible to distinguish between water samples from Quaternary and Miocene aquifers. Relatively low ⁸⁷Sr/⁸⁶Sr ratios, i.e., ∼0.7083, in Sr-rich water samples indicate that the majority of dissolved Sr in groundwater from Miocene as well as Quaternary strata is probably derived from Miocene marine skeletal carbonate matter in the subsurface. This situation is probably the result of Quaternary glacial reworking of upper Tertiary material and/or hydraulic contact between Quaternary and Miocene aquifers. A positive correlation between Sr contents and non-volatile organic carbon indicates that the remarkably high contents of organic matter recorded in these aquifers almost certainly are derived from Miocene sources as well. Received, February 1999 / Revised, July 1999 / Accepted, July 1999     

Constraining the marine strontium budget with natural strontium isotope fractionations (Sr/Sr∗, δSr) of carbonates, hydrothermal solutions and river waters

We present strontium (Sr) isotope ratios that, unlike traditional ⁸⁷Sr/⁸⁶Sr data, are not normalized to a fixed ⁸⁸Sr/⁸⁶Sr ratio of 8.375209 (defined as δ^88/86Sr = 0 relative to NIST SRM 987). Instead, we correct for isotope fractionation during mass spectrometry with a ⁸⁷Sr-⁸⁴Sr double spike. This technique yields two independent ratios for ⁸⁷Sr/⁸⁶Sr and ⁸⁸Sr/⁸⁶Sr that are reported as (⁸⁷Sr/⁸⁶Sr∗) and (δ^88/86Sr), respectively. The difference between the traditional radiogenic (⁸⁷Sr/⁸⁶Sr normalized to ⁸⁸Sr/⁸⁶Sr = 8.375209) and the new ⁸⁷Sr/⁸⁶Sr∗ values reflect natural mass-dependent isotope fractionation. In order to constrain glacial/interglacial changes in the marine Sr budget we compare the isotope composition of modern seawater ((⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_Seawater) and modern marine biogenic carbonates ((⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_Carbonates) with the corresponding values of river waters ((⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_River) and hydrothermal solutions ((⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_HydEnd) in a triple isotope plot. The measured (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_River values of selected rivers that together account for ∼18% of the global Sr discharge yield a Sr flux-weighted mean of (0.7114(8), 0.315(8)‰). The average (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_HydEnd values for hydrothermal solutions from the Atlantic Ocean are (0.7045(5), 0.27(3)‰). In contrast, the (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_Carbonates values representing the marine Sr output are (0.70926(2), 0.21(2)‰). We estimate the modern Sr isotope composition of the sources at (0.7106(8), 0.310(8)‰). The difference between the estimated (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_input and (⁸⁷Sr/⁸⁶Sr∗, δ^88/86Sr)_output values reflects isotope disequilibrium with respect to Sr inputs and outputs. In contrast to the modern ocean, isotope equilibrium between inputs and outputs during the last glacial maximum (10-30 ka before present) can be explained by invoking three times higher Sr inputs from a uniquely “glacial” source: weathering of shelf carbonates exposed at low sea levels. Our data are also consistent with the “weathering peak” hypothesis that invokes enhanced Sr inputs resulting from weathering of post-glacial exposure of abundant fine-grained material.     

Hydrogeochemistry and strontium isotopes of spring and mineral waters from Monte Vulture volcano,Italy

This paper describes the results of a study that was conducted to determine the relationship between hydrogeochemical composition and ⁸⁷Sr/⁸⁶Sr isotope ratios of the Mt. Vulture spring waters. Forty samples of spring waters were collected from local outcrops of Quaternary volcanites. Physico-chemical parameters were measured in the field and analyses completed for major and minor elements and ⁸⁷Sr/⁸⁶Sr isotopic ratios. A range of water types was distinguished varying from alkaline-earth bicarbonate waters, reflecting less intense water–rock interaction processes to alkali bicarbonate waters, probably representing interaction with volcanic rocks of Mt. Vulture and marine evaporites. The average ⁸⁷Sr/⁸⁶Sr isotope ratios suggest at least 3 different sources. However, some samples have average Sr isotope ratios (0.70704–0.70778) well above those of the volcanites. These ratios imply interaction with other rocks having higher ⁸⁷Sr/⁸⁶Sr ratios, probably Triassic evaporites, which is substantiated by their higher content of Na, SO₄ and Cl. The Sr isotope ratios for some samples (e.g. Toka and Traficante) are intermediate between the value for the Vulture volcanites and that for the local Mesozoic rocks. The salt content of these samples also lies between the value for waters interacting solely with the volcanites and the value measured in the more saline samples. These waters are thus assumed to result from the mixing of waters circulating in volcanic rocks with waters presumably interacting with the sedimentary bedrock (marine evaporites).     

Possible causes of quasiperiodic variations in geomagnetic reversal frequency and Sr/Sr ratios in marine carbonates through the Phanerozoic

Variations in frequency of geomagnetic reversals through the Phanerozoic have been analyzed jointly with ⁸⁷Sr/ ⁸⁶Sr ratios in marine carbonate sediments. The time series of both parameters contain principal components with periods from 90 to 110 Ma and show a certain correlation. Namely, (i) both time series have five local minimums spaced at similar intervals (period lengths); (ii) the minimums in the Δ⁸⁷Sr/⁸⁶Sr curve follow in time those of the reversal frequency, with a lag from 12 Myr in the Ordovician to 38 Myr in the Cretaceous; (iii) the rate of heat transfer from processes at the core-mantle boundary (in D″ layer) which control the Earth's geological life was from 7 to 25 cm/yr in the Phanerozoic. This rate approaches the observed velocities of horizontal plate motion and the predicted mantle convection rates.     

Paleoclimate reconstruction based on the timing of speleothem growth and oxygen and carbon isotope composition in a cave located in the rain shadow in Israel

High-resolution ²³⁰Th/²³⁴U ages and δ¹⁸O and δ¹³C compositions of speleothems in Ma’ale Efrayim Cave located to the east of the central mountain ridge of Israel enable us to examine the nature of the rain shadow aridity during glacial and interglacial intervals. Speleothem growth occurred during marine glacial isotopic periods, with no growth during the two last marine isotope interglacial intervals and during the peak of the Last Glacial Maximum. This contrasts with speleothem growth in caves located on the western flank of the central mountain ridge, in the Eastern Mediterranean semiarid climatic zone, which continued throughout the last 240,000 yr. Thus, during glacial periods water reached both sides of the central mountain ridge. A comparison of the present-day rain and cave water isotopic compositions and amounts at the Ma’ale Efrayim Cave site with those on the western flank shows that evaporation and higher temperatures on the eastern flank are major influences on isotopic composition and the lack of rainfall. The δ¹⁸O and δ¹³C profiles of the speleothems deposited between 67,000 and 25,000 yr B.P. match the general trends of the isotopic profiles of Soreq Cave speleothems, suggesting a similar source (eastern Mediterranean Sea) and similar climatic conditions. Thus, during glacial periods the desert boundary effectively migrated further south or east from its present-day location on the eastern flank, whereas interglacial periods appear to have been similar to the present, with the desert boundary at the same position. The decrease in overall temperature and a consequent reduction in the evaporation to precipitation ratios on the eastern flank are viewed as the major factors controlling the decay of the rain shadow effect during glacial periods.     

Typical Geochemical Elements in Loess Deposit in the Northeastern Tibetan Plateau and Its Paleoclimatic Implication

Widespread and thick loess deposit in the northeastern Tibetan Plateau records paleoclimatic changes over the Quaternary period. In this study, we investigate a loess section located in a high terrace of the Huangshui River in the Xining Basin, and collect samples at 20-cm intervals by digging a well of 16-m depth （including paleosol S1 and SO and several loess interlayers over the last glacial-interglacial cycle and the Holocene）. Concentration of some active elements （Sr and Ca） and inert elements （Rb, Zr, Ti） in these loess samples are measured. The results show that ratios of those elements （oxide）, such as Rb/Sr, Ti/Sr, and Zr/CaO ratios, would indicate sensitively paleoclimatic changes, especially the history of precipitation over the last glacial-interglacial and the Holocene. Moreover, the curves of Rb/Sr, Ti/Sr, and Zr/CaO ratios had almost the same variable trends from the bottom to the top and also closely correlated with values of magnetic susceptibility and the global marine δ^18O record. But compared with the curves of magnetic susceptibility, the changes of ratios of these elements （oxide） are clearer and easy to understand. Therefore, the ratios of these typical chemical elements in the loess deposit may be used as an excellent index to investigate the history of paleoclimate, particularly precipitation changes in the northeastern Tibetan Plateau.     

Fluxes of Sr into the headwaters of the Ganges

Himalayan weathering is recognized as an important agent in modifying sea water chemistry, but there are significant uncertainties in our understanding of Himalayan riverine fluxes. This paper examines causes of the variability, including that of the seasons, by analysis of downstream variations in Sr, ⁸⁷Sr, and major ions in the mainstream, in relation to the composition of tributary streams from subcatchments with differing geologic substrates.Water samples were collected over four periods spanning the premonsoon, monsoon, and postmonsoon seasons. Uncertainties in the relative fluxes have been estimated, using Monte Carlo techniques, from the short-term variability of mainstream chemistry and the scatter of tributary compositions. The results show marked seasonal variations in the relative inputs related to high monsoon rainfall in the High and Lesser Himalaya, contrasting with the major contribution from glacial melt waters from the Tibetan Sedimentary Series (TSS) at times of low rainfall. Much of the spread in previously published estimates of the sources of Sr in Himalayan rivers may result from these seasonal variations in Sr fluxes.The annual fluxes of Sr into the headwaters of the Ganges are derived from the three main tectonic units in the proportions 35 ± 1% from the TSS, 27 ± 3% from the High Himalayan Crystalline Series (HHCS), and 38 ± 8% from the Lesser Himalaya. The particularly elevated ⁸⁷Sr/⁸⁶Sr ratios characteristic of the HHCS and the Lesser Himalaya enhance their influence on seawater Sr-isotope composition. The TSS contributes 13 ± 1%, the HHCS 30 ± 3%, and the Lesser Himalaya 57 ± 11% of the ⁸⁷Sr flux in excess of the seawater ⁸⁷Sr/⁸⁶Sr ratio of 0.709.     

Reconstructing the migration patterns of late Pleistocene mammals from northern Florida, USA

We used analyses of the strontium isotope (⁸⁷Sr/⁸⁶Sr) ratios of tooth enamel to reconstruct the migration patterns of fossil mammals collected along the Aucilla River in northern Florida. Specimens date to the late-glacial period and before the last glacial maximum (pre-LGM). Deer and tapir displayed low ⁸⁷Sr/⁸⁶Sr ratios that were similar to the ratios of Florida environments, which suggest that these taxa did not migrate long distance outside of the Florida region. Mastodons, mammoths, and equids all displayed a wide range of ⁸⁷Sr/⁸⁶Sr ratios. Some individuals in each taxon displayed low ⁸⁷Sr/⁸⁶Sr ratios that suggest they ranged locally, while other animals had high ⁸⁷Sr/⁸⁶Sr ratios that suggest they migrated long distances (> 150 km) outside of the Florida region. Mastodons were the only taxa from this region that provided enough well-dated specimens to compare changes in migration patterns over time. Pre-LGM mastodons displayed significantly lower ⁸⁷Sr/⁸⁶Sr ratios than late-glacial mastodons, which suggests that late-glacial mastodons from Florida migrated longer distances than their earlier counterparts. This change in movement patterns reflects temporal changes in regional vegetation patterns.     

Late Quaternary climatic control on erosion and weathering in the eastern Tibetan Plateau and the Mekong Basin

High-resolution siliciclastic grain size and bulk mineralogy combined with clay mineralogy, rubidium, strontium, and neodymium isotopes of Core MD01-2393 collected off the Mekong River estuary in the southwestern South China Sea reveals a monsoon-controlled chemical weathering and physical erosion history during the last 190,000 yr in the eastern Tibetan Plateau and the Mekong Basin. The ranges of isotopic composition are limited throughout sedimentary records: ⁸⁷Sr/⁸⁶Sr = 0.7206–0.7240 and ε_Nd(0) = −11.1 to −12.1. These values match well to those of Mekong River sediments and they are considered to reflect this source region. Smectites/(illite + chlorite) and smectites/kaolinite ratios are used as indices of chemical weathering rates, whereas the bulk kaolinite/quartz ratio is used as an index of physical erosion rates in the eastern Tibetan Plateau and the Mekong Basin. Furthermore, the 2.5–6.5 μm/15–55 μm siliciclastic grain size population ratio represents the intensity of sediment discharge of the Mekong River and, in turn, the East Asian summer monsoon intensity. Strengthened chemical weathering corresponds to increased sediment discharge and weakened physical erosion during interglacial periods. In contrast, weakened chemical weathering associated with reduced sediment discharge and intensified physical erosion during glacial periods. Such strong glacial–interglacial correlations between chemical weathering/erosion and sediment discharge imply the monsoon-controlled weathering and erosion.     

Strontium isotope variations in lower tertiary-quaternary volcanic rocks from the Kurile island arc

Average ⁸⁷Sr/⁸⁶Sr ratios for lavas from Quaternary and Pleistocene volcanoes of the Kurile island arc, NW Pacific, decrease from 0.7035 in the south to 0.7032 in the north. The northern Kuriles are characterised by K₂Oricher volcanics and by an older crust. Varying ratios show no simple relation to crustal thickness or geochemical indicators of crustal contamination. This is thought to reflect the immature character of the crust — its simatic composition, low Rb/Sr ratios and youthfulness. Older lavas from the Kuriles (Lower Tertiary, Miocene) have similar or slightly higher ⁸⁷Sr/⁸⁶Sr ratios; some have suffered slight alteration and possibly crustal contamination. Quaternary volcanics from the Kurile and Aleutian arcs have the lowest ⁸⁷Sr/⁸⁶Sr ratios of all circum-Pacific arcs and this may be ascribed to (a) the isotopic individuality of the landward North American plate and/or (b) the high degree of mechanical coupling between the Pacific and North American plates reducing the amount of subducted ⁸⁷Sr-rich sediments and seawater. An isotopic boundary between island arcs is located in central Hokkaido. The primary basaltic magmas of the Kuriles were derived from mantle recently contaminated by radiogenic Sr. Subsequent fractionation to andesites and dacites occurred by closed-system fractional crystallization.     

A strontium isotopic study of the volcanic rocks of the Myoko volcano group,central Japan

Thirty-one selected volcanic rocks from the Myoko volcano group which comprises a volcanic chain of four independent volcanoes of Quaternary to Recent age are analyzed for ⁸⁷Sr/⁸⁶Sr ratios. The rocks of the lizuna volcano, the oldest among the Myoko volcano group, have higher ⁸⁷Sr/⁸⁶Sr ratios and show a larger scatter ranging from 0.7043₇ to 0.7055₆ than those of other volcanoes. The Kurohime volcanic rocks have a restricted range of ⁸⁷Sr/⁸⁶Sr ratios (0.7040₃∼0.7043₅). ⁸⁷Sr/⁸⁶Sr ratios of the Myoko volcanic rocks are almost the same in average to those of the Kurohime volcanic rocks, although somewhat varied ranging from 0.7037₈ to 0.7046₁. A single analysis of the Yakeyama volcanic rock yielded a ⁸⁷Sr/⁸⁶Sr ratio of 0.7042₇. A characteristic pattern in ⁸⁷Sr/⁸⁶Sr ratios is observed through the volcanic activity of the Myoko volcano group; ⁸⁷Sr/⁸⁶Sr ratios are high in the early stage of the volcanic activity and then decrease to low values, the late eruptives being characterized by constant ⁸⁷Sr/⁸⁶Sr ratios. The negative correlation between ⁸⁷Sr/⁸⁶Sr and Rb/Sr, and positive correlation between ⁸⁷Sr/⁸⁶Sr and Sr found in the rocks of the Iizuna volcano are interpreted to show the occurrence of contamination by materials with high ⁸⁷Sr/⁸⁶Sr ratios (>0.7056), low Rb/Sr ratios (<0.01) and high Sr contents (>300 ppm). Sialic crustal contamination may have played only a minor role.     

Strontium isotopic evidence on the chemical evolution of pore waters in the Milk River Aquifer,Alberta, Canada

Strontium isotope ratios were measured on 13 rock, 18 leachate and 28 pore-water samples from the Milk River aquifer, the confining argillaceous formations, and the glacial till mantling the recharge area. Strontium isotope ratios (⁸⁷Sr/⁸⁶Sr) of pore waters from the aquifer, confining units, and the glacial till ranged from 0.7069 to 0.7082. The ⁸⁷Sr/⁸⁶Sr ratios in aquifer pore waters decrease with increasing distance from the aquifer recharge area, and this is interpreted to be the result of mixing and water–rock interaction within the aquifer.The solute composition of the recharging groundwater is modified by the local lithology, causing distinct geochemical patterns along different flow paths within the aquifer. Whole-rock ⁸⁷Sr/⁸⁶Sr ratios indicate that the shales and till are generally more radiogenic than the aquifer sandstone. The authigenic carbonate cements and rock-forming minerals comprising the major lithologic units had little apparent influence on the pore-water Sr chemistry. Carbonate cement leachates from the till and the aquifer sandstone are more radiogenic than those from the confining shale formations. Feldspar separates from the aquifer sandstone have relatively radiogenic Sr isotope ratios, whereas bentonites from the Milk River and Colorado Shale Formations have whole-rock and leachate Sr isotope ratios that are relatively unradiogenic. Ratios of most Milk River aquifer pore waters are lower than those of any leachates or whole rocks analyzed, except the bentonites.The ⁸⁷Sr/⁸⁶Sr ratios of exchangeable Sr in the bentonites are similar to ratios found in the more evolved pore waters. Simple rock–water interaction models calculated for the whole-rock, leachate, and exchangeable-ion/pore-water pairs indicate that ion exchange with bentonite clays within the Milk River and Colorado Shale Formations appears to influence the isotopic evolution of the pore-water Sr in each of these units.     

Sr isotopic and elemental characteristics of calcites in the Chinese deserts: Implications for eolian Sr transport and seawater Sr evolution

Calcite content, Sr concentrations, and isotopes of calcites in the Chinese deserts are systematically studied in this paper. Calcite contents, which are calculated according to acid-soluble Ca contents in the deserts, are generally higher in the sandy deserts than in the sandy lands and decrease roughly from northwest to northeast of China. Acid-soluble Sr is well correlated with calcite in the Chinese deserts, implying acid-soluble Sr comes mainly from the calcite dissolution. Sr concentrations in calcites, calculated on the basis of calcite contents and acid-soluble Sr concentrations in the deserts, have an inverse relation to calcite contents, essentially mirroring the degree of Sr substitution for Ca in the calcite development. Desert calcites have regional variations in Sr isotopic ratios. Calcite Sr isotopic ratios depend on geological settings and chemical weathering. The Badain Jaran, and Tengger deserts are probably affected by additional factors such as the remote groundwater cycle or overturning of underlying sand deposits.Only four deserts (Taklimakan, Qaidam, Badain Jaran, and Tengger) appear to be potential sources of eolian deposits in the Chinese Loess Plateau (CLP). Isotopic signatures of calcite Sr and silicate Nd further indicate that the Tengger desert was not an important source for eolian deposits in the CLP. Eolian calcite was probably enriched due to wind sorting from the potential sources to the CLP and suffered weathering–leaching after it accumulated in the CLP. Sr isotopic compositions and Ca/Sr molar ratios of calcites are different between the deserts and the Lingtai profile, due to the integrated effect of wind sorting and weathering–leaching.It is essential to calculate accurately the ⁸⁷Sr/⁸⁶Sr ratio and Sr concentration of eolian calcite entering the oceans according to geochemical data of the Chinese deserts, because of the importance of the Chinese deserts in the global dust cycle. The calculated Sr concentration and ⁸⁷Sr/⁸⁶Sr ratio of eolian calcite entering the North Pacific Ocean, are 11.75 μmol/g and 0.71032, respectively. The calculated values in this study are close to the recommended values by Jacobson [Jacobson A. D. (2004) Has the atmospheric supply of dissolved calcite dust to seawater influenced the evolution of marine ⁸⁷Sr/⁸⁶Sr ratios over the past 2.5 million years? Geochem. Geophys. Geosyst. 5(12), 1–9, Q12002. doi:10.1029/2004GC000750]. Using the same model as that of Jacobson (2004), the effect of Asia dust on the evolution of seawater Sr isotopes is evaluated. (⁸⁷Sr/⁸⁶Sr)_seawater increases by 0.3 × 10⁻⁵ if the lower dust flux of 2.34 × 10⁸ mol Sr/yr is used in the model, suggesting the little effect of Asian dust on the seawater Sr record in the Quaternary. The increase in (⁸⁷Sr/⁸⁶Sr)_seawater is 1.5 × 10⁻⁵ if the higher value of 1.17 × 10⁹ mol Sr/yr is used, as observed in the Quaternary Sr record. These results further support the suggestions of Jacobson (2004).     

Late Quaternary river terrace sequences in the eastern Kunlun Range,northern Tibet: A combined record of climatic change and surface uplift

The Kunlun Range, a reactivated orogenic belt, constitutes the northern margin of the Tibetan Plateau. The extreme relief and major landforms of the Kunlun Range are a product of late Cenozoic tectonics and erosion. However, well-developed late Quaternary terraces that occur along the northern slope of the Kunlun Range probably resulted from climatic change rather than surface uplift. The terrace sequences formed in thick Quaternary valley fills and have total incision depths of 50–60 m. Optically stimulated luminescence dating was employed to place time controls on the valley fills and associated terraces. Dating results suggest that periods of significant aggradation were synchronous between different rivers and correspond to the last glacial stage. The abrupt change from aggradation to incision occurred between 21.9 ± 2.7 and 16 ± 2.2 ka, coincident with the last glacial–interglacial transition. Additional terraces developed during the late glacial period and early to middle Holocene. Based on a broader set of chronological data in northern Tibet, at least four regional incision periods can be recognized. Chronological data, terrace elevation profiles, and climate proxy records suggest that these terracing periods were triggered by cool and/or wet climatic conditions. A geometric survey of the riverbed longitudinal profile suggests that surface uplift serves as a potential dynamic forcing for long-term incision. A model is proposed for terrace formation as a response to climatic perturbation in an uplifted mountain range.     

中国第四纪冰期、地文期和黄土记录

中国第四纪冰川的发育受岩石圈运动造成的三大地貌阶梯的严格控制,主要出现在最高阶梯的青藏高原和西北山地,第二阶梯以下分布零星。把冰期、地文期和黄土记录结合起来研究会迅速提高中国第四纪冰川的研究水平。兰州附近有三次古冰川遗迹,分别可以和T₁、T₂、T₃和T₄相应。相当于氧同位素2、4、6和16阶段,即70,000—10,000aB.P.、0.15MaB.P.和0.6MaB.P.。     

Determination of Sr/Sr mass-dependent isotopic fractionation and radiogenic isotope variation of Sr/Sr in the Neoproterozoic Doushantuo Formation

We measured both mass-dependent isotope fractionation of δ⁸⁸Sr (⁸⁸Sr/⁸⁶Sr) and radiogenic isotopic variation of Sr (⁸⁷Sr/⁸⁶Sr) for the Neoproterozoic Doushantuo Formation that deposited as a cap carbonate immediately above the Marinoan-related Nantuo Tillite. The δ⁸⁸Sr and ⁸⁷Sr/⁸⁶Sr compositions showed three remarkable characteristics: (1) high radiogenic ⁸⁷Sr/⁸⁶Sr values and gradual decrease in the ⁸⁷Sr/⁸⁶Sr ratios, (2) anomalously low δ⁸⁸Sr values at the lower part cap carbonate, and (3) a clear correlation between ⁸⁷Sr/⁸⁶Sr and δ⁸⁸Sr values. These isotopic signatures can be explained by assuming an extreme greenhouse condition after the Marinoan glaciation. Surface seawater, mixed with a large amount of freshwater from continental crusts with high ⁸⁷Sr/⁸⁶Sr and lighter δ⁸⁸Sr ratios, was formed during the extreme global warming after the glacial event. High atmospheric CO₂ content caused sudden precipitation of cap carbonate from the surface seawater with high ⁸⁷Sr/⁸⁶Sr and lighter δ⁸⁸Sr ratios. Subsequently, the mixing of the underlying seawater, with unradiogenic Sr isotope compositions and normal δ⁸⁸Sr ratios, probably caused gradual decrease of the ⁸⁷Sr/⁸⁶Sr ratios of the seawater and deposition of carbonate with normal δ⁸⁸Sr ratios. The combination of ⁸⁷Sr/⁸⁶Sr and δ⁸⁸Sr isotope systematics gives us new insights on the surface evolution after the Snowball Earth.     

The strontium isotopic composition and origin of burial cements in the Lincolnshire Limestone (Bajocian) of central Lincolnshire, England

Strontium isotopic composition (⁸⁷Sr/⁸⁶Sr) of two petrographically, chemically and isotopically (δ¹⁸O and δ¹³C) distinct phases of burial calcites from the Lincolnshire Limestone are indistinguishable (0.70820± 26). The mean ⁸⁷Sr/⁸⁶Sr ratio of these phases is considerably more radiogenic than ⁸⁷Sr/⁸⁶Sr ratios of Bajocian marine waters (～0.70725). Neither Bajocian marine waters nor meteoric waters buffered by host marine carbonate in the Limestone could have precipitated the burial spars. Radiogenic strontium may have been contributed from K-feldspar dissolution and/or clay recrystallization, either within clastic portions of the Limestone itself, or from major clastic units adjacent to the Limestone. Alternatively, Palaeozoic marine waters or remobilized Palaeozoic marine carbonate and/or sulphate could have supplied the necessary radiogenic strontium.     

Late Quaternary glacial–interglacial variations in sediment supply in the southern Drake Passage

Geochemical characteristics of marine sediment from the southern Drake Passage were analyzed to reconstruct variations in sediment provenance and transport paths during the late Quaternary. The 5.95 m gravity core used in this study records paleoenvironmental changes during the last approximately 600 ka. Down-core variations in trace element, rare earth element, and Nd and Sr isotopic compositions reveal that sediment provenance varied according to glacial cycles. During glacial periods, detrital sediments in the southern Drake Passage were mostly derived from the nearby South Shetland Islands and shelf sediments. In contrast, interglacial sediments are composed of mixed sediments, derived from both West Antarctica and East Antarctica. The East Antarctic provenance of the interglacial sediments was inferred to be the Weddell Sea region. Sediment input from the Weddell Sea was reduced during glacial periods by extensive ice sheets and weakened current from the Weddell Sea. Sediment supply from the Weddell Sea increased during interglacial periods, especially those with higher warmth such as MIS 5, 9, and 11. This suggests that the influence of deep water from the Weddell Sea increases during interglacial periods and decreases during glacial periods, with the degree of influence increasing as interglacial intensity increases.