Isotopic constraints on growth conditions of multiphase calcite–pyrite–barite concretions in Carboniferous mudstones

Carbonate concretions in the Lower Carboniferous Caton Shale Formation contain diagenetic pyrite, calcite and barite in the concretion matrix or in different generations of septarian fissures. Pyrite was formed by sulphate reduction throughout the sediment before concretionary growth, then continued to form mainly in the concretion centres. The septarian calcites show a continuous isotopic trend from δ¹³C=?28·7‰ PDB and δ¹⁸O=?1·6‰ PDB through to δ¹³C=?6·9‰ PDB and δ¹⁸O=?14·6‰ PDB. This trend arises from (1) a carbonate source initially from sulphate reduction, to which was added increasing contributions of methanogenic carbonate; and (2) burial/temperature effects or the addition of isotopically light oxygen from meteoric water. The concretionary matrix carbonates must have at least partially predated the earliest septarian cements, and thus used the same carbonate sources. Consequently, their isotopic composition (δ¹³C=?12·0 to ?10·1‰ PDB and δ¹⁸O=?5·7 to ?5·6‰ PDB) can only result from mixing a carbonate cement derived from sulphate reduction with cements containing increasing proportions of carbonate from methanogenesis and, directly or indirectly, also from skeletal carbonate. Concretionary growth was therefore pervasive, with cements being added progressively throughout the concretion body during growth. The concretions contain barite in the concretion matrix and in septarian fissures. Barite in the earlier matrix phase has an isotopic composition (δ³⁴S=+24·8‰ CDT and δ¹⁸O=+16·4‰ SMOW), indicating formation from near‐surface, sulphate‐depleted porewaters. Barites in the later septarian phase have unusual isotopic compositions (δ³⁴S=+6 to +11‰ CDT and δ¹⁸O=+8 to +11‰ SMOW), which require the late addition of isotopically light sulphate to the porewaters, either from anoxic sulphide oxidation (using ferric iron) or from sulphate dissolved in meteoric water. Carbon isotope and biomarker data indicate that oil trapped within septarian fissures was derived from the maturation of kerogen in the enclosing sediments.     

Climatic control of fluvial-lacustrine cyclicity in the Cretaceous Cordilleran Foreland Basin, western United States

Tectono-stratigraphic models of foredeep sedimentation have generally presumed a direct link between changing rates of tectonism and concomitant sedimentological response as manifested by change in thickness, composition or depositional environment of sediment accumulating in adjacent basins. Lacustrine limestone units within the early Cretaceous fluvial/lacustrine Gannett Group of western Wyoming exhibit systematic variation in several geochemical proxies of relative rates of precipitation and evaporation, indicating that lakewater chemistry was controlled by variation in regional climate. Change in proportion of allochthonous terrigenous clastic vs. autochthonous carbonate deposition, as well as carbonate Mg/Ca ratio and stable isotopic composition, occurs at two scales. Metre-scale alternation of micritic limestone and argillaceous marl is accompanied by mineralogical and isotopic variation within individual beds, indicating preferential carbonate accumulation during intervals of decreased regional meteoric precipitation relative to lake-surface evaporation. Limestone deposition began during intervals of maximum aridity, and decreased as increased meteoric precipitation-driven flux of terrigenous clastic sediment overwhelmed sites of carbonate accumulation. Similar upsection variation in limestone mineralogy and isotopic composition at a scale of tens of metres reflects the multiple processes of long-term increase in meteoric precipitation and lakewater freshening prior to influx of terrigenous sediment, across-basin fluvial-deltaic progradation, and renewed accumulation of riverine terrigenous units. Such trends suggest that formation-scale alternation between fluvial clastic and lacustrine carbonate deposition was controlled by climate change.     

Water chemistry and sedimentological observations in littlefield lake,michigan: Implications for lacustrine marl deposition

A combination of both water chemistry and sedimentological information was used to investigate the carbonate-producing mechanism in Littlefield Lake, a small lake located in Isabella County, central Michigan. Data on temperature, dissolved oxygen, pH, calcium carbonate (CaCO₃) saturation, alkalinity, calcium, and magnesium were obtained on a monthly basis over a 13-month period, with each parameter determined at 1m intervals over a depth range of 20m. The loss of dissolved carbon dioxide (CO₂) from warm surface waters during direct degassing, and to a lesser extent during photosynthetic uptake by lacustrine macrophytes and phytoplankton during the summer, results in massive precipitation of the low-magnesium calcite which predominates in all Littlefield Lake sedimentary facies However, despite the fact that carbonate precipitation in this rather typical temperate-region marl lake is directly related to, and may be driven by, seasonal variation in these physiochemical parameters, most calcite forms as encrustations around cyanophytic and chlorophytic macrophytes. Such relationships demonstrate that carbonate precipitation in marl lakes may result from complex interactions between both biochemical and physiochemical processes. As such, marl formation in this, and probably many other calcareous lake systems, can not be simply ascribed to one or the other of these two general mechanisms.     

桂林地区大气降水（大雨、暴雨）的δ18O特征与水汽来源的关系

现代大气降水中的稳定同位素组成是全球或地区性水循环研究的重要载体,同时也是冰芯、湖泊沉积物、石笋等研究领域中,运用稳定同位素来重建古气候的重要依据。本文研究了桂林地区2012年大气降水氢氧同位素组成的逐日变化,根据得到的132组氢氧稳定同位素组成建立了桂林局地大气降水线方程为δD = 8.8δ18O +17.96,大气降水的δ18O波动范围在-13.56‰～+1.07‰,平均为-5.78‰;δD在-101.52‰～+16.02‰,δD平均为-41.03‰。利用降水稳定同位素资料,结合后向轨迹法( Backwards Trajectory) 对桂林水汽来源进行追踪,发现夏季(5-10月)大气降水的水汽来源主要受来自孟加拉湾、南海海洋气团的水汽源的控制,降水的δ18O值偏负,平均为-8.02‰(共64组);冬季(11月至次年4月)大气降水的水汽来源主要受来自西太平洋暖湿气团、冬季风冷气团或西风环流所携带的大陆性气团的影响,不同程度地叠加了局地环流气团、蒸发水汽的补给的影响,降水的δ18O值偏正,平均为-2.86‰(共68组)。研究结果表明,桂林大气降水的稳定同位素组成与降水的水汽来源、季风类型、降水云团来源和性质有关,来自远距离输送夏季风海洋性水汽团形成的降水δ18O值较低(或偏负), 而大陆性气团或局地蒸发水汽循环形成的降水δ18O值较高（或偏正）。不同的水汽来源是决定降水中δ18O值变化的主要因素,因此,通过降水中的δ18O值,特别是其季节变化的特征分析,可以反过来揭示当地降水的水汽来源。      

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.     

Isotope geochemistry, petrology and depositional environments of the diatomite-dominated Tripoli Formation (Lower Messinian), Sicily

ABSTRACT The Tripoli Formation (Lower Messinian) in Sicily includes diatomites irregularly alternating with marl and carbonate beds and lies, stratigraphically, between the Tortonian pelagic marls and the evaporitic Calcare di base. The relationships between mineralogy, textural features and oxygen-carbon isotopic compositions of carbonate components point to a wide variability of depositional conditions and suggest that Tripoli sedimentation occurred in small basins characterized by periodic and marked restriction from the open sea.
The isotopic values of calcite and dolomite in the diatomites suggest an evolution from normal marine towards more restricted environments. Evaporating conditions are also indicated by the occurrence of anhydrite, length-slow chalcedonic quartz and moulds of gypsum. In a more advanced stage, the precipitation of heavy δ¹⁸0 dolomite in the interstitial pores of fossil-poor diatomites denotes an environment with highly evaporated water. Mixing of meteoric and marine waters, on the other hand, might have favoured the precipitation of a dolomite characterized by relatively low δ¹⁸0 and δ¹³C values.
The deposition of marl and carbonate beds alternating with or overlying the diatomites took place in an environment with highly evaporated marine waters on the basis of δl¹⁸O values of dolomite (up to + 9.10‰) and aragonite (up to + 5.83‰), occurrence of evaporitic minerals and lack of fossils. The presence at these levels of calcite with extremely negative δ¹³C values (down to - 38.40‰), filling gypsum moulds, suggests activity of sulphate-reducing bacteria. Some aragonitic marls, however, bear evidence of deposition in relatively normal marine conditions.     

A Late Weichselian stable isotope stratigraphy compared with biostratigraphical data: A case study from southern Sweden

Late Weichselian lake sediments from a site in southern Sweden, were analysed for stable carbon and oxygen isotopes, as well as plant macrofossils and insect remains. By comparison of independent data sets, general climatic changes were demonstrated. Lithological, chemical and stable isotope data reveal two significant climatic oscillations at ca. 12 200–12 000 and ca. 11 000–10 200 yr BP respectively. Continental climatic conditions, indicated by evaporative enrichment of ¹⁸O in lake marl, characterise parts of the early lake history, including the Older Dryas Stadial. Distinct variations of δ¹³C in organic material is discussed in terms of climatically induced changes in lake-water chemistry. Different types of photosynthetic assimilation of dissolved inorganic carbon is proposed as a contributing factor influencing lake marl δ¹³C. The universal application of a positive correlation between lake marl δ¹⁸O and mean annual air temperature is questioned. Quantifications of mean summer and winter temperatures based on beetle analysis show a climatic optimum around 12 000 yr BP, a marked cooling around 11 000 yr BP and a strong amelioration at ca. 10 200 yr BP. These climatic events were accompanied by distinct changes in aquatic vegetation. Plant macrofossil and insect analyses indicate an open vegetation during the entire period studied. Biostratigraphical data reflecting local limnic and terrestrial vegetation and regional climate facilitate the interpretation of stable isotope data.     

伊犁河谷大气降水同位素特征及环境意义

为研究伊犁谷地降水同位素特征及陆地内循环对其的影响,为流域水循环研究提供科学依据,于2016年在伊宁、尼勒克和新源气象站采集降水同位素样品。采用回归对照法,讨论降水氘氧稳定同位素的影响因素。研究表明,研究区大气降水线方程为δD=7.96δ^18O+10.37,与全球大气降水线较接近,水汽主要由西风带输送;氘氧同位素夏季富集冬季贫化而氘盈余无规律变化,由于降水过程不仅受温度效应,还受到水汽陆地再循环影响。冬夏季样品在D-^18O关系图中分布特征,证明冬夏影响降水同位素本地水循环因素不同,夏季以云下蒸发为主。根据对氘过量计算的夏季降水雨滴蒸发分数为4.1%~16.2%,再次证明夏季云下蒸发效应明显,而在冬季云下蒸发效应几乎不会发生。     

成都地区大气降水稳定同位素组成反应的气候特征

分析了1986-1998年成都地区大气降水的稳定同位素组成。夏季降水的δD和δ^18O值比冬季降水轻,反映了季风气候的降水特点。成都地区的大气降水线方程是：δD=1．42＋7．530δ^18O,与全球和中国降水线方程相比,表明了成都地区的蒸发程度稍大于降雨,说明成都地区大气降水的不平衡蒸发程度弱,反映了海洋性气候特征。成都地区大气降水δ^18O与降雨量、温度和水汽压之间都是负相关关系。但是降雨量对大气降水δ^18O的影响最大。     

桂林洞穴滴水与现代碳酸钙δ18O记录的环境意义--以桂林七星岩NO.15支洞为例

现代洞穴动态监测的一个先决条件就是为洞穴碳酸盐(CaCO₃)沉积物-石笋的各种替代指标的解译提供可靠的依据,充分利用现代碳酸盐(CaCO₃)沉积物的各种替代指标,并与现代器测气象资料进行相互对比、并用以校正,是精确或定量解释石笋气候替代指标的关键.
经对桂林七星岩15号支洞的5个滴水点进行了长达四个水文年(2008~2011年)的大气降水、洞穴滴水、现代碳酸盐沉积物的动态监测和研究,并探讨了洞穴滴水和现代碳酸盐(CaCO₃)的δ18O与降水δ18O的相关关系.研究表明,洞穴滴水和现代碳酸盐(CaCO₃)的年平均δ18O值非常接近降水的δ18O平均值,并具有与地表降水δ18O相同的变化趋势,反映了洞穴滴水和现代碳酸盐(CaCO₃)的δ18O主要来自大气降水的δ18O,即明显受控于降水的δ18O.在4个水文年中,现代洞穴次生化学碳酸盐(CaCO₃)沉积物的δ18O值与滴水的δ18O值记录的年内(或年际)变化或多年的变化趋势基本相同,表现出明显的四高峰(δ18O低值区)四低谷(δ18O高值区)的波动变化特征,具有明显的年际、季节性变化规律,显示具有雨热同季的特点.研究结果表明洞穴滴水和洞穴现代碳酸盐(CaCO₃)沉积物的δ18O可以记录当地或洞穴上方的气候变化信号,即现代碳酸盐(CaCO₃)沉积物的δ18O主要作为夏季风强度或降雨量的替代指标.     

达里诺尔湖水体稳定氢、氧同位素组成变化对结冰过程的响应

利用自然界中广泛分布的环境同位素进行湖泊水体演化过程分析已经成为现代湖泊科学的重要研究方向.通过采集内蒙古达里诺尔湖(简称"达里湖") 2013年1月份的湖冰、湖水, 2012年夏季湖水与湖区大气降水等, 共分析了77个样品中稳定氢(H)、氧(O)同位素值的变化情况, 在此基础上对达里湖水体稳定H、O同位素组成变化及其对结冰过程的响应进行了详细分析, 结果显示: (1)伴随结冰过程的完成, 各站点深层冰体(厚度~65 cm)中δD、δ18O值比表层冰体(厚度~15 cm)中的值出现不同幅度的偏重.而冰下水体中δD、δ18O平均值则比冰体中的平均值分别偏轻约13.85‰、2.23‰.在冰层形成的快速与稳定阶段, δD、δ18O值的变化幅度也存在差异.同时, 冬季外源水体的输入对各站点间同位素值差异的影响比夏季更明显; (2)夏季湖水、冬季湖水与湖冰的同位素值均落在全球大气降水线与湖区大气降水线之外, 显示湖泊冰封之前, 蒸发对湖泊水体同位素偏移存在一定程度的影响; 而冬季湖水与湖冰的同位素值基本位于同一斜率区间, 且全部落在夏季湖水同位素值的右侧, 显示两者之间并不存在明显的蒸发分馏作用, 造成上述现象的因素只能归结于结冰过程.      

博斯腾湖全新世岩芯沉积物碳酸盐氧同位素气候意义

西风影响区全新世气候变化逐渐受到重视。但目前该区高精度定年和气候意义明确的代用指标仍然缺乏。利用西风影响区新疆博斯腾湖BST04H钻孔岩芯沉积物全新世自生碳酸盐(细颗粒沉淀碳酸盐和介形虫壳体)氧同位素,结合该区降水同位素分布特征和流域水文状况,分析该区湖泊沉积物碳酸盐氧同位素的气候意义,并与湖泊不同位置钻孔碳酸盐氧同位素指标进行对比。结果表明,博斯腾湖深水区沉积物自生碳酸盐氧同位素主要反映了区域的降水(入流)/蒸发比,并保留了入流水体同位素组成的变化信息。全新世自8100cal.aB.P.以来,氧同位素呈现出在波动中逐渐偏正的长期变化趋势,中全新世以后波动幅度加大,其间氧同位素值偏负的波动并不完全指示有效湿度增加,而是入湖水体同位素变化,并与湖泊的水文状况有关。这种波动在湖泊西部距离入湖河口位置较近的钻孔中表现得更为明显。不同位置钻孔同位素变化有很好的对应性,但不同位置相同时段内的波动幅度不一样。实际研究中应充分对比分析,深入理解指标的意义,防止仅依靠某一个位置的指标将这种局地波动信息解释成代表大范围区域的气候或环境信息。     

Lake carbonate-δ18O records from the Yukon Territory,Canada: Little Ice Age moisture variability and patterns

A 1000-yr history of climate change in the central Yukon Territory, Canada, is inferred from sediment composition and isotope geochemistry from small, groundwater fed, Seven Mile Lake. Recent observations of lake-water δ¹⁸O, lake level, river discharge, and climate variations, suggest that changes in regional effective moisture (precipitation minus evaporation) are reflected by the lake’s hydrologic balance. The observations indicate that the lake is currently ¹⁸O-enriched by summer evaporation and that during years of increased precipitation, when groundwater inflow rates to the lake increase, lake-water δ¹⁸O values decrease. Past lake-water δ¹⁸O values are inferred from oxygen isotope ratios of fine-grained sedimentary endogenic carbonate. Variations in carbonate δ¹⁸O, supplemented by those in carbonate and organic δ¹³C, C/N ratios, and organic carbon, carbonate and biogenic silica accumulation rates, document changes in effective moisture at decadal time scales during the early Little Ice Age period to present. Results indicate that between ～AD 1000 and 1600, effective moisture was higher than today. A shift to more arid climate conditions occurred after ～AD 1650. The 19th and 20th centuries have been the driest of the past millennium. Temporal variations correspond with inferred shifts in summer evaporation from Marcella Lake δ¹⁸O, a similarly small, stratified, alkaline lake located ～250 km to the southwest, suggesting that the combined reconstructions accurately document the regional paleoclimate of the east-central interior. Comparison with regional glacial activity suggests differing regional moisture patterns during early and late Little Ice Age advances.     

华北地区大气降水稳定同位素特征与水汽来源

选取华北地区的包头,石家庄,天津,太原IAEA/WMO/GNIP大气降水的氢氧同位素组成的资料,分析了华北地区降水稳定同位素的时空分布特征及其影响因素.研究表明:华北地区降水中的δ18O值都表现出明显的“夏高冬低”的季风气候特征,夏季表现雨量效应,冬季温度效应明显;华北各地区降水线方程与全国及全球降水线相比,斜率和截距都偏小,揭示了华北地区降水是在非瑞利条件下进行的,并且除天津外,其他地区稳定同位素特征还受到降水过程中局地水汽循环的影响;d值总体表现出冬高夏低的季节变化特征,说明了冬季风和夏季风期间降水的水源区蒸发条件不同.     

Changes in carbon and oxygen isotope composition during limestone diagenesis

The calcite fossils of the Derbyhaven Beds, Isle of Man, have δ¹³C values (+ 1·8 PDB) similar to modern, shallow-water marine skeletons, but the δ¹⁸O values (?6·1 PDB) are much lighter than modern skeletons. The light oxygen values indicate either re-equilibration with isotopically light water before cementation started, or Carboniferous sea water with δ¹⁸O of ?6‰. Aragonite dissolution was followed by precipitation of zoned calcite cement. In this cement, up to six intracrystalline zones, recognized in stained thin sections, show isotopic variation. Carbon varies from + 3-8 to + 1-2‰. and oxygen from ? 2-6 to ? 12-4‰. with decreasing age of the cement. This trend is attributed to increasing temperature and to isotopic evolution of the pore waters during burial. The zoned calcite is sequentially followed by dolomite and kaolinite cements which continue the trend towards light isotopic values. This trend is continued with younger, fault-controlled dolomite, and is terminated by vein-filling calcite and dolomite. The younger calcite, interpreted as a near-surface precipitate from meteoric waters, is unrelated to the older sequence of carbonates and has distinctly different carbon isotope ratios: δ¹³C ? 6-8‰.     

Oxygen and Hydrogen Isotopes of Waters in the Ordos Basin,China: Implications for Recharge of Groundwater in the North of Cretaceous Groundwater Basin

Hundreds of precipitation samples collected from meteorological stations in the Ordos Basin from January 1988 to December 2005 were used to set up a local meteoric water line and to calculate weighted average isotopic compositions of modern precipitation. Oxygen and hydrogen isotopes, with averages of ?7.8‰ and ?53.0‰ for δ18O and δD, respectively, are depleted in winter and rich in spring, and gradually decrease in summer and fall, illustrating that the seasonal effect is considerable. They also show that the isotopic difference between south portion and north portion of the Ordos Basin are not obvious, and the isotope in the middle portion is normally depleted. The isotope compositions of 32 samples collected from shallow groundwater (less than a depth of 150 m) in desert plateau range from ?10.6‰ to ?6.0‰ with an average of ?8.4‰ for δ18O and from ?85‰ to ?46‰ with an average of ?63‰ for δD. Most of them are identical with modern precipitation. The isotope compositions of 22 middle and deep groundwaters (greater than a depth of 275 m) fall in ranges from ?11.6‰ to ?8.8‰ with an average of ?10.2‰ for δ18O and from ?89‰ to ?63‰ with an average of ?76‰ for δD. The average values are significantly less than those of modern precipitation, illustrating that the middle and deep groundwaters were recharged at comparatively lower air temperatures. Primary analysis of 14C shows that the recharge of the middle and deep groundwaters started at late Pleistocene. The isotopes of 13 lake water samples collected from eight lakes define a local evaporation trend, with a relatively flat slope of 3.77, and show that the lake waters were mainly fed by modern precipitation and shallow groundwater.     

An alternative model for positive shifts in shallow-marine carbonate δ13C and δ18O

Abstract Positive shifts in global seawater δ¹³C_DIC are related to changes in the ratio of organic relative to inorganic carbon burial in oceanic basins, whereas factors such as climatic cooling and the accumulation of polar ice are known to cause positive shifts in δ¹⁸O. Here, an alternative model is proposed for the formation of local positive isotope shifts in shallow-marine settings. The model involves geochemically altered platform-top water masses and the effects of early meteoric diagenesis on carbonate isotopic composition. Both mechanisms are active on modern (sub)tropical carbonate platforms and result in low carbonate δ¹³C and δ¹⁸O relative to typical oceanic values. During high-amplitude transgressive events, the impact of isotopically light meteoric fluids on the carbonate geochemistry is much reduced, and ¹³C-depleted platform-top water mixes with open oceanic water masses having higher isotope values. Both factors are recorded as a transient increase in carbonate ¹³C and ¹⁸O relative to low background values. These processes must be taken into consideration when interpreting the geochemical record of ancient epeiric seas.     

三水盆地古近系湖相沉积岩的氧、碳同位素地球化学记录及其环境意义

三水盆地古近系莘庄组顶部至土布心组红岗段的全岩碳酸盐稳定同位素分析结果表明其形成期间经历了多次环境变迁。根据碳酸盐氧、碳同位素比值及其相互关系的变化,可识别三次海水入侵期。其时δ18O值大幅度向正值漂移。而由于受有机质降解的影响,相应时期的δ13 C均表现为低值。在不直接受海洋影响的湖相沉积阶段,δ18O与δ13 C的相关程度虽然未达到典型的封闭型湖泊水平,但仍呈现一定的正相关变化 (r =0.6 5 ),表明其湖水滞留时间较长。而频繁出现的石膏薄层沉积也指示湖盆的封闭性较好。这些均表明这一时期的三水盆地可能是一周期性封闭型湖泊。其稳定同位素组成主要受制于蒸发量/降雨量平衡的变化。而δ13 C比值往往还受有机质活动的控制,更多的是反映有机质生产力、埋藏与降解率。     

High‐resolution diatom δ18O records,from the last 150 years,reflecting changes in amount of winter precipitation in two sub‐Arctic high‐altitude lakes in the Swedish Scandes

Waters from high‐altitude alpine lakes are mainly recharged by meteoric water. Because of seasonal variations in precipitation and temperature and relatively short hydraulic residence times, most high‐altitude lakes have lake water isotopic compositions (δ¹⁸O_lake) that fluctuate due to seasonality in water balance processes. Input from snowmelt, in particular, has a significant role in determining lake water δ¹⁸O. Here we compare two high‐resolution δ¹⁸O_diatom records from lake sediments in the Swedish Scandes with instrumental data from the last century obtained from nearby meteorological stations. The time period AD 1900–1990 is characterised by an increase in winter precipitation and high winter/summer precipitation ratios and this is recorded in δ¹⁸O_diatom as decreasing trends. Lowest δ¹⁸O_diatom values and highest amount of winter precipitation are found around AD 1990 when the winter North Atlantic Oscillation index was above +2. We conclude that for the last 150 a the main factor affecting the δ¹⁸O_diatom signal in these sub‐Arctic high‐altitude lakes with short residence times has been changes in amount of winter precipitation and that δ¹⁸O_diatom derived from high‐altitude lakes in the Swedish Scandes can be used as a winter precipitation proxy. Copyright © 2010 John Wiley & Sons, Ltd.     

淡水软体动物壳质氧同位素组成与气候环境

研究现代及第四纪淡水软体动物一些属种的氧同位素组成,显示如下规律:与海相软体动物相比,淡水软体动物富集轻氧同位素组成,δ16<-5‰;相同水域生活的不同属种的氧同位素组成相差较小（萝卜螺等例外）,不同水域生活的软体动物壳质氧同位素相差较大;全贝壳氧同位素主要继承生活时的水体的氧同位素组成,受气候干湿程度影响;第四纪化石也富集轻氧同位素组成,δ16O分布范围较宽;湿润期,化石富集16O,凉干期,化石富集16O。