Evaluation of oxygen isotopes in carbonate as an indicator of lake evolution in arid areas: The modern Qinghai Lake, Qinghai–Tibet Plateau

The oxygen isotopic composition of carbonate in lakes has been used as a useful indicator in Palaeolimnological research, and has made some important contributions to our understanding of lacustrine systems. For modern lakes in arid or cold areas, however, there are few data available to test the effect of lake salinity and temperature on the oxygen isotopic composition of various carbonate sources such as ostracod, bulk carbonate, and fine-grained carbonate (< 60 μm). Here we examined the oxygen isotopic composition of ostracods, bulk carbonate, and fine-grained carbonates, as well as that of coexisting water from Lake Qinghai and the smaller surrounding lakes and ponds on the Qinghai–Tibet Plateau. Our investigation highlights three key effects. First, the oxygen isotopic composition of ostracods, bulk carbonate, and fine-grained carbonate in the lakes and ponds shows a clear response to lake water δ¹⁸O values, and these vary with water salinity. The relationship between lake water δ¹⁸O and salinity is not only dominated by the evaporation/freshwater input ratios, but is also controlled by the distance to the mouth of the major rivers supplying to the lake. Second, the ostracod, bulk carbonate, and fine-grained carbonate show similar isotopic change trends in the study area, and oxygen isotopic differences between ostracods and authigenic carbonate may be explained by the different water temperatures and very small ‘vital offsets’ of ostracods. Finally, the effect of water depth on temperature leads to increasing δ¹⁸O values in carbonates as water depth increases, both in benthic ostracods living on the lake bottom, as well as in bulk carbonate precipitated at the water surface.For arid, high-altitude Lake Qinghai, our results suggest that variations in the δ¹⁸O values of carbonate in Lake Qinghai are mainly controlled by the oxygen-isotope ratio of the lake water changing with water salinity. As a secondary effect, increasing water depth leads to cooler bottom and surface water, which may result in more positive δ¹⁸O values of ostracod and bulk carbonate.     

新疆玛纳斯湖沉积物氧同位素记录的古气候信息探讨──与青海湖和色林错比较

内陆封闭湖泊自生碳酸盐氧同位素组成与大气降水同位素组成、空气相对湿度和地面气温这三个参数相关。我国季风带的青海湖与色林错的δ¹⁸O曲线非常相似,说明古气候变化受相同因素驱动。在10500～9500aB．P．的末次冰期向全新世的过渡期,这两个湖泊的δ¹⁸O值大幅度下降,这是夏季风雨水的低δ¹⁸O值的缘故。属于西风带的玛纳斯湖和季风带的青海湖的δ¹⁸O曲线基本上是对称的。大约9500～4000aB．P,图形由对称转变为相似,据此推论当时夏季风的影响范围可能达到新疆北部。     

Controls on ostracod valve geochemistry, Part 1: Variations of environmental parameters in ostracod (micro-)habitats

The variations of environmental conditions (T°, pH, δ¹³C_DIC, [DIC], δ¹⁸O, Mg/Ca, and Sr/Ca) of ostracod habitats were examined to determine the controls of environmental parameters on the chemical and isotopic composition of ostracod valves. Results of a one-year monitoring of environmental parameters at five sites, with depths of between 2 and 70 m, in Lake Geneva indicate that in littoral to sub-littoral zones (2, 5, and 13 m), the chemical composition of bottom water varies seasonally in concert with changes in temperature and photosynthetic activity. An increase of temperature and photosynthetic activity leads to an increase in δ¹³C values of DIC and to precipitation of authigenic calcite, which results in a concomitant increase of Mg/Ca and Sr/Ca ratios of water. In deeper sites (33 and 70 m), the composition of bottom water remains constant throughout the year and isotopic values and trace element contents are similar to those of deep water within the lake. The chemical composition of interstitial pore water also does not reflect seasonal variations but is controlled by calcite dissolution, aerobic respiration, anaerobic respiration with reduction of sulphate and/or nitrate, and methanogenesis that may occur in the sediment pores. Relative influence of each of these factors on the pore water geochemistry depends on sediment thickness and texture, oxygen content in bottom as well as pore water. Variations of chemical compositions of the ostracod valves of this study vary according to the specific ecology of the ostracod species analysed, that is its life-cycle and its (micro-)habitat. Littoral species have compositions that are related to the seasonal variations of temperature, δ¹³C values of DIC, and of Mg/Ca and Sr/Ca ratios of water. In contrast, the compositions of profundal species are largely controlled by variations of pore fluids along sediment depth profiles according to the specific depth preference of the species. The control on the geochemistry of sub-littoral species is a combination of controls for the littoral and profundal species as well as the specific ecology of the species.     

Environmental Evolution of the Water Body of Qinghai Lake since the Postglacial Age

Based on the data developed from various s natural waters in the Qinghai Lake area and ostracode shells present in drill core QH-16A of recent lake-floor sediments ,this paper discusses the distribution of stable isotopes in the modern water body of Qinghai Lake,and the initial isotopic composition of the lake water has been deduced ,Studies of δ^18O,δ^13C,Mg/Ca and Sr/Ca in ostracode shells provide the basis for the establishment of the model of climatic fluctuation in the Qinghai Lake area since the postaglacial age,as well as for the elucidation of the environmental evolution of the water body of Qinghai Lake since the postglacial age.     

Climatic change recorded by stable isotopes and trace elements in a British Holocene tufa

Combined stable isotope (δ¹⁸O and δ¹³C) and trace element (Mg, Sr) geochemistry from bulk tufa calcite and ostracod shell calcite from an early Holocene British tufa reveal clear records of Holocene palaeoclimatic change. Variation in δ¹⁸O is caused principally by change in the isotopic composition of Holocene rainfall (recharge), itself caused mainly by change in air temperature. The δ¹³C variability through much of the deposit reflects increasing influence of soil‐zone CO₂, owing to progressive woodland soil development. Bulk tufa Mg/Ca and Sr/Ca are controlled by their concentrations in the spring water. Importantly, Mg/Ca ratios are not related to δ¹⁸O values and thus show no temperature dependence. First‐order sympathetic relationships between δ¹³C values and Mg/Ca and Sr/Ca are controlled by aquifer processes (residence times, CO₂ degassing and calcite dissolution/reprecipitation) and probably record intensity of palaeorainfall (recharge) effects. Stable isotope records from ostracod shells show evidence of vital effects relative to bulk tufa data. The ostracod isotopic records are markedly ‘spiky’ because the ostracods record ‘snapshots’ of relatively short duration (years), whereas the bulk tufa samples record averages of longer time periods, probably decades. The δ¹⁸O record appears to show early Holocene warming, a thermal maximum at ca. 8900 cal. yr BP and the global 8200 yr BP cold event. Combined δ¹³C, Mg/Ca and Sr/Ca data suggest that early Holocene warming was accompanied by decreasing rainfall intensity. The Mg/Ca data suggest that the 8200 yr BP cold event was also dry. Warmer and wetter conditions were re‐established after the 8200 yr BP cold event until the top of the preserved tufa sequence at ca. 7100 cal. yr BP. Copyright © 2004 John Wiley & Sons, Ltd.     

Carbonate stable isotope signals in the 1-Ma sedimentary record of the HDP-04 drill core from Lake Hovsgol, NW Mongolia

Oxygen and carbon stable isotope ratios in carbonates from the HDP-04 drill core from Lake Hovsgol, NW Mongolia, show an overall covariant relationship suggesting that for the most of the past 1 Ma Hovsgol remained a closed-basin lake. Carbonate δ¹⁸O ratio is responsive to regional climate change: a ca. +1.5‰ basinwide δ¹⁸O shift has occurred with the onset of Bølling–Allerød warming (sensu lato), followed by a ca. 0.8‰ depletion during the Younger Dryas. The post-glacial δ¹⁸O shift of the same magnitude is recorded in bulk carbonates, shells of two ostracod species and in wet-sieved fine fraction <63 μm. Associated with the lake-level rise and correlative with the post-glacial warming in the northern hemisphere, the observed δ¹⁸O shift is nevertheless positive. This argues against changes in local temperature and hydrology as key driving mechanisms. Most likely, Lake Hovsgol δ¹⁸O reflects a climate-driven shift in the composition of regional precipitation. Tied into a distinct lithologic succession, the radiocarbon-dated late glacial δ¹⁸O shift apparently represents a ‘template’ of the lake's response to glacial–interglacial transitions: a similar pattern of parallel changes in lithology and carbonate stable isotope composition is observed in at least 10 more intervals in the 1-Ma record, including the MIS 20/MIS19 transition at the Brunhes/Matuyama paleomagnetic reversal boundary. The comparison of carbon stable isotope ratios of untreated and in vacuo roasted bulk sediment with those of detrital carbonates suggests that clastic input of carbonates by lake tributaries does not affect the geochemistry of bulk carbonates in the HDP-04 section. The profiles of bulk carbonate δ¹⁸O and δ¹³C in the Pleistocene section of the HDP-04 drill core suggest at ca. 15.4 ka, at ca. 100 m below today's level, Lake Hovsgol still stood relatively high as compared with prior extended periods of time during late Matuyama and early Brunhes. Isotopically heavy δ¹⁸O and δ¹³C ratios during the mid–late Brunhes, particularly, in carbonate crusts and oolites, are suggestive of past episodes of dramatic evaporative ¹⁸O-enrichment of lake waters. Despite the expectation of muted amplitudes of temperature- and precipitation-related isotope signals, the sedimentary record from the sensitive ‘water gauge’ basin of Lake Hovsgol has high potential for providing important constraints on past hydrologic evolution of continental interior Asia during the Pleistocene.     

青藏高原中部色林错中晚全新世以来古气候变化特征

色林错位于青藏高原中部印度季风和西风环流的过渡地带，同时受西风环流和印度季风系统控制，是研究二者进退变化特征的理想场所。本文利用色林错SL 1钻孔中介形虫 Limnocythere inopinata 的丰度及其壳体微量元素Mg/Ca和Mn/Ca比值重建了色林错5. 3 ka BP以来的古气候环境变化特征。5. 3~2. 9 ka BP， L. inopinata 丰度较小，壳体的低Mg/Ca比值和高Mn/Ca比值表明此阶段气候偏冷湿；2. 9~1. 8 ka BP， L. inopinata 丰度较前一阶段增加，壳体Mg/Ca比值略有增长但仍为低值表明气温虽然有所回升但仍然较低，Mn/Ca比值较前一阶段明显降低，指示湖泊水位下降；1. 8 ka BP至今， L. inopinata 丰度达到最大，壳体的高Mg/Ca和Mn/Ca比值指示湖泊温度和水位均呈显著的上升趋势。通过与西风区、过渡区以及印度季风区其他湖泊的环境沉积记录对比，本文认为青藏高原中部地区在中全新世晚期主要受西风环流影响，气温较低，西风带来大量水汽使得湖面呈扩张趋势；而到晚全新世西风环流逐渐北撤，色林错受季风影响更大，季风带来的降水和气温升高导致的冰川融水增加与色林错水位上升有密切关系。     

Calcium-isotope fractionation in selected modern and ancient marine carbonates

The calcium-isotope composition (δ^44/42Ca) was analyzed in modern, Cretaceous and Carboniferous marine skeletal carbonates as well as in bioclasts, non-skeletal components, and diagenetic cements of Cretaceous and Carboniferous limestones. In order to gain insight in Ca²⁺_aq-CaCO₃-isotope fractionation mechanisms in marine carbonates, splits of samples were analyzed for Sr, Mg, Fe, and Mn concentrations and for their oxygen and carbon isotopic composition. Biological carbonates generally have lower δ^44/42Ca values than inorganic marine cements, and there appears to be no fractionation between seawater and marine inorganic calcite. A kinetic isotope effect related to precipitation rate is considered to control the overall discrimination against ⁴⁴Ca in biological carbonates when compared to inorganic precipitates. This is supported by a well-defined correlation of the δ^44/42Ca values with Sr concentrations in Cretaceous limestones that contain biological carbonates at various stages of marine diagenetic alteration. No significant temperature dependence of Ca-isotope fractionation was found in shells of Cretaceous rudist bivalves that have recorded large seasonal temperature variations as derived from δ¹⁸O values and Mg concentrations. The reconstruction of secular variations in the δ^44/42Ca value of seawater from well preserved skeletal calcite is compromised by a broad range of variation found in both modern and Cretaceous biological carbonates, independent of chemical composition or mineralogy. Despite these variations that may be due to still unidentified biological fractionation mechanisms, the δ^44/42Ca values of Cretaceous skeletal calcite suggest that the δ^44/42Ca value of Cretaceous seawater was 0.3-0.4‰ lower than that of the modern ocean.     

Ostracod Mg/Sr/Ca and 87Sr/86Sr geochemistry from Tibetan lake sediments: Implications for early to mid‐Pleistocene Indian monsoon and catchment weathering

Jin, Z. D., Bickle, M. J., Chapman, H. J., Yu, J., An, Z., Wang, S. & Greaves, M. J. 2010: Ostracod Mg/Sr/Ca and ⁸⁷Sr/⁸⁶Sr geochemistry from Tibetan lake sediments: Implications for early to mid‐Pleistocene Indian monsoon and catchment weathering. Boreas, 10.1111/j.1502‐3885.2010.00184.x. ISSN 0300‐9483 Lacustrine sediment serves as a valuable archive for tracing catchment weathering processes associated with past climatic and/or tectonic changes. High‐resolution records of fossil ostracod Mg/Ca, Sr/Ca and ⁸⁷Sr/⁸⁶Sr ratios from a lake sediment core from the central Tibetan Plateau reveal a temporal link between lake‐water chemistry and catchment weathering and distinct monsoonal oscillations over the early to mid‐Pleistocene. Between 2.01 and 0.95 Ma, lake‐water chemistry was dominated by a high proportion of carbonate weathering related to variations in the Indian monsoon, resulting in relatively low and constant ostracod ⁸⁷Sr/⁸⁶Sr but obvious fluctuations in Mg/Ca, Sr/Ca and δ¹⁸O. Across the mid‐Pleistocene transition (MPT), a significant increase in ⁸⁷Sr/⁸⁶Sr and frequently fluctuating ratios of ostracod Mg/Ca, Sr/Ca and δ¹⁸O are coincident with increases in both Chinese loess grain size and Arabian Sea lithogenic flux. This correlation indicates an increased glaciation and a strong monsoon seasonal contrast over the plateau. The increase in lake‐water ⁸⁷Sr/⁸⁶Sr across the MPT highlights a change in catchment weathering patterns, rather than one in climate‐enhanced weathering intensity, with an increased weathering of ⁸⁷Sr‐rich minerals potentially induced by marked extensive glaciation and strong seasonality in the central plateau.     

Lithium isotopes in foraminifera shells as a novel proxy for the ocean dissolved inorganic carbon (DIC)

Past ocean pH and pCO₂ are critical parameters for establishing relationships between Earth's climate and the carbon cycle. Previous pCO₂ estimates are associated with large uncertainties and are debated. In this study, laboratory cultures of the foraminiferan genus Amphistegina were performed in order to examine the possible factors that control the Li isotope composition (δ⁷Li) of their shells. δ⁷Li is insensitive to temperature and pH variations but correlates positively with the Dissolved Inorganic Carbon (DIC) of seawater. Li/Ca ratio in the shells shows negative correlation with δ⁷Li, consistent with published data for planktonic foraminifera from core tops and from short periods during the Cenozoic. We propose that the sensitivity of δ⁷Li and Li/Ca ratio to DIC is a biological phenomenon and is related to biomineralization mechanisms in foraminifera. We used the published foraminiferal δ⁷Li records, and our experimental results, to determine the paleo-ocean DIC and pH for the last glacial–interglacial cycle. The results are consistent with published estimates of pH and pCO₂ based on boron isotopes and ice cores. We suggest Li and its isotopes may serve as a new complementary proxy for the paleo-ocean carbonate chemistry.     

A first look at oxygen isotope records from modern and Holocene-aged gastropod (Stenomelania) shells from Lake Kutubu,Papua New Guinea

The oxygen isotopic composition of Stenomelania gastropod shells was investigated to reconstruct Holocene palaeoclimate change at Lake Kutubu in the southern highlands of Papua New Guinea. Oxygen isotope (δ¹⁸O) values recorded in aquatic gastropod shells change according to ambient water δ¹⁸O values and temperature. The gastropod shells appear to form in oxygen isotopic equilibrium with the surrounding water and record a shift in average shell oxygen isotopic composition through time, probably as a result of warmer/wetter conditions at ca. 600–900 and 5900–6200 cal a bp. Shorter term fluctuations in oxygen isotope values were also identified and may relate to changes in the intensity or source of rainfall. Further δ¹⁸O analyses of gastropod shells or other carbonate proxies found in the Lake Kutubu sediments are warranted. © 2020 John Wiley & Sons, Ltd.     

Mg/Ca, Sr/Ca, and stable isotopes in modern and Holocene Protothaca staminea shells from a northern California coastal upwelling region

This study explores the potential of intertidal Protothaca staminea shells as high-resolution geochemical archives of environmental change in a coastal upwelling region. Mg/Ca and Sr/Ca ratios were analyzed by excimer laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS) at sub-weekly temporal resolution in shells growing ∼1 mm per month. Growth patterns of a modern P. staminea shell from Humboldt Bay, California, collected in December 1999 made it possible to infer a lifespan from 1993 to 1998. Growth hiatuses in the shell may have excluded records of extreme events. Mg/Ca ratios appeared to be partly controlled by water temperature; the correlation coefficient between temperature and Mg/Ca was r = 0.71 in one of four growth increments. Significant year-to-year differences in the sensitivity of Mg/Ca to temperature in P. staminea could not be explained, however. Sr/Ca ratios appeared to be more closely related to shell growth rate. Oxygen isotopes, measured at 2-week temporal resolution in the same shell, did not show a clear relation to local temperature in summer, possibly because temperatures were higher and less variable at the King Salmon mudflat, where the shell was collected, than in the main channel of Humboldt Bay, where water properties were monitored. Negative shell δ¹³C values (<−0.5‰) marked spring and summer coastal upwelling events.The Mg contents of P. staminea midden shells dated to ∼3 ka and ∼9 ka were significantly lower than in the modern shell. This may have resulted from degradation of a Mg-rich shell organic matrix and precluded quantitative interpretation of the older high-resolution records. Elevated δ¹³C values in the ∼3 ka shell suggested that the individual grew in highly productive or stratified environment, such as a shallow coastal embayment or lagoon.     

Stable 18O and 13C isotope records of Viviparus diluvianus (Kunth, 1865) shells from Holsteinian (MIS 11) lakes of eastern Poland as palaeoenvironmental and palaeoclimatic proxies

The oxygen and carbon stable isotope composition of Viviparus diluvianus shells was determined in the palaeolakes of the Holsteinian interglacial (MIS 11) in eastern Poland: the Ortel Królewski, Hrud, Ossówka, Roskosz and Szymanowo lakes. The occurrence of V. diluvianus covers the Taxus zone, the so‐called intra‐interglacial cooling period (Pinus‐Larix zone), the climatic optimum (Carpinus‐Abies zone) and the post‐optimal period with an undefined pollen zone. The isotope record of V. diluvianus shells allowed palaeoclimate and palaeoenvironmental reconstructions. δ¹⁸O and δ¹³C vary from −8.7‰ in the post‐optimal period to −4.8‰ in the optimal period, and from −10.6‰ at the beginning of the Taxus zone to −4.2‰ at the climatic optimum, respectively. A positive correlation of the isotope curves indicates closed‐water bodies, and only at Roskosz was some occasional overflow inferred. Higher oxygen isotopes correspond to an increase in temperature and/or enhanced evaporation, which is well marked in the Carpinus‐Abies zone, whereas samples enriched in ¹³C are correlated with periods demonstrating a lower water level and higher productivity in the lakes. Episodes of lake shallowing and dense aquatic vegetation occurred in the Pinus‐Larix zone and during the climatic optimum. The isotope ratios for the climatic optimum significantly exceed those of the other periods, thus pointing to warmer conditions. An estimation of relative changes of average summer temperatures using the δ¹⁸O/temperature gradient yielded variation of 1–2 °C within the lakes. Absolute temperature reconstructions indicate the effects of specific local conditions. Hence, V. diluvianus shells offer a reliable proxy in qualitative studies of interglacial lake records.     

Constraints on water chemistry by chemical weathering in the Lake Qinghai catchment, northeastern Tibetan Plateau (China): clues from Sr and its isotopic geochemistry

Lake water, river water, and groundwater from the Lake Qinghai catchment in the northeastern Tibetan Plateau, China have been analyzed and the results demonstrate that the chemical components and ⁸⁷Sr/⁸⁶Sr ratios of the waters are strictly constrained by the age and rock types of the tributaries, especially for groundwater. Dissolved ions in the Lake Qinghai catchment are derived from carbonate weathering and part from silicate sources. The chemistry of Buha River water, the largest tributary within the catchment, underlain by the late Paleozoic marine limestone and sandstones, constrains carbonate-dominated compositions of the lake water, being buffered by the waters from the other tributaries and probably by groundwater. The variation of ⁸⁷Sr/⁸⁶Sr ratios with cation concentrations places constraint on the Sr-isotopic compositions of the main subcatchments surrounding Lake Qinghai. The relative significance of river-water sources from different tributaries (possibly groundwater as well) in controlling the Sr distribution in Lake Qinghai provides the potential to link the influence of hydrological processes to past biological and physical parameters in the lake. The potential role of groundwater input in the water budget and chemistry of the lake emphasizes the need to further understand hydrogeological processes within the Lake Qinghai system.     

Stable isotopic compositions of Recent freshwater cyanobacterial carbonates from the British Isles: local and regional environmental controls

Recent (<50 years old) freshwater cyanobacterial carbonates from diverse environments (streams, lakes, waterfalls) throughout Britain and Ireland were analysed for their stable carbon and oxygen isotope compositions. The mean δ¹⁸O value of ?5–9‰ PDB for river and stream data represents calcite precipitation in equilibrium with the mean oxygen isotopic composition of precipitation in central Britain (?7–5‰SMOW) assuming a mean water temperature of 9°C. The mean δ¹⁸O of lake data, ?4–5‰ PDB, is statistically different, reflecting the effects of residence time and/or variations in the oxygen isotopic composition of rainfall. Carbon isotopes have wide variations in both fluviatile and lake data sets (+ 3 to ?12‰ PDB). These variations are principally controlled in the fluviatile samples by contribution of isotopically light ‘soil zone’ carbon relative to isotopically heavier carbon from limestone aquifer rock dissolution. Lake samples have the heaviest carbon isotope values, reflecting a trend toward isotopic equilibrium between atmospheric CO₂ and aqueous HCO^?₃. We infer that isotopic compositions of ancient cyanobacterial carbonates should also record environmental information, although the effects of stabilization and diagenesis on primary δ¹⁸O values will need careful consideration. Primary carbon isotope compositions should be well preserved, although in marine samples values will be buffered by the isotopic composition of aqueous marine bicarbonate.     

Characteristics of the change of major lakes on the Qinghai Tibet Plateau in the last 25 years

On the Qinghai-Tibet Plateau there are three super large lakes, the Qinghai Lake, Nam Co and Siling Co, and eleven large lakes, the Zhari Nam Co, Tangra Yumco, Ayakkum Lake, Banggong Co, Har Lake, Ngoring Lake, Yamzho Yumco, Gyaring Lake, Chibuzhang Co, Ulan Ul Lake and the Ngangla Ringco. The authors studied the changes of these major lakes in the past 25 years, based on interpretations of the MSS images obtained during the middle 1970s and ETM⁺ images obtained in the late 1990s or at the beginning of the 21st century. The study shows that: the areas of the Har Lake andNgoring Lake have remained relatively stable; the areas of the Qinghai Lake, Zhari Nam co, Tangra Yumco, Ayakkum Lake, Gyaring Lake, Ulan Ul Lake and Ngangla Ringco have been reduced to varying degrees, of which the areas of the Qinghai Lake and Ulan Ul Lake have decreased most sharply by 60.60 km² and 59.80 km² respectively; the areas of the Nam Co, Siling Co and Bangong Co have increased more or less, of which the area of the Siling Co has increased most sharply by 140.42 km². The analysis on the changes in areas of major lakes has provided new materials for the study of the lake evolution, climatic change and environmental variation on the Qinghai-Tibet Plateau. __________ Translated from Geological Bulletin of China, 2007, 26(12): 1633–1645 [译自: 地质通报]     

Speleothem stable isotope records interpreted within a multi-proxy framework and implications for New Zealand palaeoclimate reconstruction

A primary step in the interpretation of speleothem stable isotope records (¹⁸O/¹⁶O and ¹³C/¹²C) is to conduct a comparison with other local palaeoclimate proxies. Here, two new master speleothem δ¹⁸O and δ¹³C records (one from eastern North Island, and the other from western/southern South Island, New Zealand) are evaluated against independent precipitation and temperature proxy information to assess their palaeoclimate reconstruction potential. This comparison also resulted in a serendipitous opportunity to reconstruct past circulation using climate regime classification [Lorrey, A.M., Fowler, A.M., Salinger, J., 2007a. Regional climate regime classification as a qualitative tool for interpreting multi-proxy palaeoclimate data spatial patterns: a New Zealand case study. Palaeo-3, in press], specifically because these two regional climate districts are hyper-sensitive to westerly circulation changes, and in many cases, exhibit contrasting climate character in response to circulation anomalies.For both the western South Island and the eastern North Island master speleothem δ¹³C records, variations tracked changes in relative regional precipitation. The δ¹⁸O master speleothem record for both regions varied with temperature change. Both records contain strong regional climate signals that suggest they have good value for palaeoclimate reconstruction. The ensuing attempt at a multi-proxy reconstruction of regional climate regimes from the compiled proxies indicates past circulation in the New Zealand sector has varied considerably during the past four millennia. Centennial-scale circulation changes for the past 4000 years are evident, and are analogous to modern Blocking, Zonal and Trough regime types [Kidson J. W., 2000. An analysis of New Zealand synoptic types and their use in defining weather regimes. International Journal of Climatology 20, 299–316] that characterise changes in present-day (prevailing) westerly circulation. This palaeoclimate reconstruction indicates modern regional climate regime classification can be extended at least as far back as the temporal coverage of the records presented here, and it can likely be improved on with better dating control and the addition of new records with higher resolution. It is also anticipated that future work will expand to include more proxy data from across New Zealand to improve the clarity of past climate regime occurrence for the Late Holocene.     

Salinity control on long-chain alkenone distributions in lake surface waters and sediments of the northern Qinghai-Tibetan Plateau, China

Long-chain alkenones in lacustrine settings are potentially excellent biomarkers for the reconstruction of past terrestrial environmental conditions, and have been found in many different types of lakes around the globe. A wider range of factors influence the occurrence and distribution of alkenones in lake sediments and waters when compared to marine systems. Lake environmental conditions, such as temperature (in particular) and salinity, are among the key factors controlling alkenone distributions in lacustrine settings. Here we investigated alkenone distribution patterns in lakes of the northern Qinghai-Tibetan Plateau, China, and their possible relationship with environmental conditions, by analyzing paired samples of suspended particulate matter in surface waters and surface sediments. Salinity of investigated lake waters ranges from almost 0 to ∼100 g/L, while temperature variation among the lakes is minimal, effectively eliminating temperature effects on the alkenone distribution patterns observed here. We show that (1) alkenone concentrations vary substantially between the lakes, yet controlling mechanisms remain elusive; (2) C₃₇/C₃₈ ratios are substantially lower in the lakes of the Qaidam Basin than in the Lake Qinghai region, probably indicating different alkenone producers in the two regions; and (3) large variations in %C_37:4 (the percentage of the C_37:4 alkenone), determined from both surface waters and sediments, are negatively correlated with salinity. We suggest that the %C_37:4 index could be used as a salinity indicator at least on a regional scale, with careful considerations of other potentially complicating factors. However, potential reasons for why salinity could significantly affect %C_37:4 values need further investigation.     

季风与西风对青藏高原全新世气候变化的影响:同位素证据

青藏高原气候变化在冰期-间冰期、千年、十年际和季节尺度上受亚洲季风和西风环流的交互影响,表现出显著的区域性特征。然而全新世以来青藏高原气候变化的机制还不甚清楚,主要原因之一是缺少指示意义明确的古气候代用指标。课题组近年来利用叶蜡氢同位素(δDwax)重建了高原东北部的青海湖、中北部的令戈错、中部的达则错、西部的班公错和阿翁错不同时间尺度的大气降水同位素记录,本文对上述工作进行总结,并结合青藏高原全新世以来已发表的其他地点的同位素和古水文记录,揭示全新世以来季风与西风对青藏高原不同区域气候变化的影响。结果表明:1)早全新世青海湖、令戈错、班公错和阿翁错4个湖泊均主要受夏季风影响,夏季风可以影响到青藏高原的大部分地区,此时夏季风在青藏高原的最北界限可能位于青海湖以北、克鲁克湖以南。2)中全新世青海湖、班公错和阿翁错受夏季风影响逐渐减弱;然而令戈错在7.0~4.5 ka水汽主要来源于西风环流。3)晚全新世青海湖和班公错受季风的影响进一步减弱;西风在3.5~1.7 ka和2.0~1.0 ka分别影响到高原中部的令戈错和达则错;晚全新世阿翁错受冰川融水补给影响降水同位素异常偏负。4)本研究表明在中晚全新世季风较弱的时期,西风能够深入到青藏高原内部地区,给高原内部地区带来冷湿的水汽。     

柴西上干柴沟组中上段介壳微量元素古环境古气候意义

介壳微量元素具有重要的沉积古环境古气候意义,结合介壳微量元素含量变化特征和介壳化石组合生态环境特征可得到柴达木盆地西部上干柴沟组中上段更为详尽的古环境古气候演化特征。柴达木盆地西部上干柴沟组中上段介壳微量元素比值Sr/Ca、Ba/Ca、U/Ca及元素Sr、Ba、U在A阶段（28.35~26.42 Ma）值较低,B阶段（26.42~23.08 Ma）值整体较高,段末值有所下降,C阶段（23.08~22.33 Ma）值明显上升,Mn/Ca和Mn值变化大致相反。A阶段Sr/Ca和Sr均值（分别为0.002 278、37.76×10-9）较低,B阶段均值（分别为0.003 347、41.46×10-9）较高,C阶段二者均值（分别为0.003 346、56.06×10-9）也较高,Ba/Ca、U/Ca、B、U有着类似的平均值变化特征,Mn/Ca和Mn值有着相反的平均值变化特征。同时相应各阶段介壳化石组合有所不同。通过介壳微量元素变化及化石组合特征,结合同期深海氧同位素及前人研究成果表明,上干柴沟组中上段柴西古湖古环境古气候演化特征为: A阶段,盐度较低和还原性较强,水位较高,气候相对温暖润湿;B阶段,整体盐度较高和氧化性较强,水位较浅,气候整体炎热干旱,段末气候干旱程度降低;C阶段,盐度和氧化性增高,湖水变浅,气候向冷干演化,响应了早中新世中国西北内陆干旱化。该地区该时段古气候主要受全球气候演化和青藏高原隆升的影响,与副特提斯海西退也有一定关系。