Evidence for centennial-scale Lateglacial and early Holocene climatic complexity from Quoyloo Meadow,Orkney, Scotland     

Rhys G. O. Timms  Ashley M. Abrook  Ian P. Matthews  Christopher P. Francis  Agnieszka Mroczkowska  Ian Candy  Stephen J. Brooks  Alice M. Milner  Adrian P. Palmer 《第四纪科学杂志》2021,36(3):339-359

The influence of the North Atlantic on the margins of Europe means the region is particularly sensitive to changes in the ocean–atmospheric system. During the Last Glacial–Interglacial Transition (16–8 cal ka bp ) this system was repeatedly disrupted, leading to a series of abrupt and short-lived shifts in climate. Despite much research, the number and magnitude of these ‘centennial-scale’ events is not well understood. To address this, we expand upon investigations at Quoyloo Meadow, Orkney, Scotland, one of the best chronologically constrained palaeoclimate records in northern Britain. By coupling stable isotope and chironomid fossil analyses with existing data, this study identifies multiple phases of centennial-scale disturbance at: c. 14.0, 11.1, 10.8, 10.5, 10.45 and 10.3 cal ka bp , with the events at 14.0 and 10.3 exhibiting a particularly pronounced cold-climate signature. During the Holocene, the strongest response to climate forcing was at c. 10.3–10.0 cal ka bp , expressed as a two-stage drop in mean July temperatures, a shift in pollen spectra indicative of ‘less-stable’ climatic regimes, and a depletion in δ¹⁸O values. We interpret this as the first reliably dated incidence of the ‘10.3-ka event’ in the British Isles and consider the wider impact of this climatic reversal in other Holocene records.  相似文献   

MC-ICP-MS锂同位素溶液分析技术与应用     

田世洪  路娜  侯增谦  苏本勋  肖燕  杨丹 《地质论评》2021,67(3):67040029-67040029

Li同位素是一种新兴的非传统稳定同位素示踪工具,在地质学、地球化学研究中具有广阔的应用前景。目前,Li同位素溶液分析技术主要采用热电离质谱仪（TIMS）和多接收电感耦合等离子质谱仪（MC-ICP-MS）,与TIMS相比,MC-ICP-MS具有分析精度高、样品量少、测试速度快等诸多优点。本研究团队近年来建立了MC-ICP-MS高精度Li同位素分析方法,在天然样品、标准物质以及石英包裹体的Li同位素测定中都取得了良好结果。以此为依托,研究团队建立了适用于西藏本地岩石成因研究的Li同位素地质端元,并将Li同位素应用于青藏高原岩石圈结构及其隆升历史、川西碳酸岩型稀土矿床富集机制、四川呷村VMS型矿床成矿流体来源和四川甲基卡硬岩型Li矿床富集机理等方面。本文比较详细地综述了这些研究进展,旨在加深对Li同位素溶液分析技术的理解,展示其在地球化学研究中的良好应用前景。  相似文献   

滇西勐兴铅锌矿床热液方解石碳氧同位素、稀土元素特征及其指示意义     

刘锦康 《地质与勘探》2021,57(4):852-864

勐兴铅锌矿床是滇西保山地块内系列低温热液矿床中的典型代表,但地质科研工作相对薄弱。由于方解石是该矿床中分布广泛且与热液活动息息相关的重要脉石矿物,其形成贯穿整个成矿过程,故对其C-O同位素及稀土元素组成特征进行系统研究,以便探讨矿床成矿流体来源及演化。结果显示,该矿床两阶段方解石的δ~(13)C_(PDB)和δ~(18)O_(SMOW)值与海相碳酸盐岩较为接近,且从阶段Ⅰ→阶段Ⅱ呈微弱下降趋势,表明成矿流体中的C主要来源于围岩碳酸盐岩的溶解,阶段Ⅱ成矿流体在与围岩反应之前可能已经发生CO2热液去气作用;阶段Ⅰ方解石的稀土总量、特征参数及配分模式与结晶灰岩较为一致,而阶段Ⅱ方解石与生物碎屑灰岩较为相似,表明阶段Ⅰ方解石中的REE主要来源于结晶灰岩,而后生物碎屑灰岩对阶段Ⅱ方解石中的稀土贡献较大。以上数据及其矿床地质特征均显示该矿床为MVT型铅锌矿床,结合区域构造演化,认为勐兴矿床的形成与中特提斯洋闭合后腾冲地块与保山地块陆陆碰撞挤压密切相关。  相似文献   

柱色谱分离-分子筛络合洗脱过程中正构烷烃单体碳同位素分馏研究     

董浩伟  赵佳玉  曾凡刚  谢曼曼  尚文郁  王淑贤  孙青 《岩矿测试》2021,(3):349-357

应用气相色谱-气体同位素质谱(GC-C-IRMS)分析正构烷烃单体碳同位素之前,需要对饱和烃样品中正构烷烃和异构烷烃进行预分离、富集,在预分离和富集过程中正构烷烃单体碳同位素是否发生分馏是高精度分析正构烷烃单体碳同位素比值(δ~(13)C)的关键。本文以正构烷烃混合溶液为对象,利用柱色谱、5■分子筛络合、环己烷-正戊烷混合溶剂两次洗脱,GC-C-IRMS分析正构烷烃单体碳同位素,研究前处理过程中正构烷烃单体碳同位素是否发生分馏。结果表明:使用柱色谱分离前后,多数正构烷烃单体碳同位素比值相差-0.2‰～0.2‰;当5■分子筛不完全络合时,未络合的正构烷烃单体碳同位素比值偏重约0.7‰,可能发生了微弱的碳同位素分馏,但并未影响洗脱后的正构烷烃单体碳同位素比值;使用环己烷-正戊烷混合溶剂洗脱前后,碳同位素比值相差-0.2‰～0.5‰,以同样方式洗脱第二次,获得的正构烷烃单体碳同位素比值与模拟样品相差-0.3‰～0.2‰。分析不同回收率(20%)正构烷烃的单体碳同位素比值,处理前后的差值基本在0.3‰以内,可见当正构烷烃回收率低至20%左右时,其单体碳同位素仍未发生明显分馏。柱色谱分离-5■分子筛络合-混合溶剂洗脱方法适用于回收率大于20%的正构烷烃单体碳同位素分析。  相似文献   

新疆奇台县黄羊山石墨矿床特征、物质来源及成因     

孙新浩  任云生  孙珍军  李作武  王承洋 《岩石学报》2021,37(6):1867-1882

黄羊山石墨矿床位于新疆东准噶尔造山带南部的卡拉麦里地区东南段,是近年来新发现的国内外首个产于花岗岩体中的超大型石墨矿床。成矿地质条件、矿床地质特征研究表明,该矿床与黄羊山碱性花岗岩体具有密切的时空及成因联系,矿石具独特的球状构造,球体中石墨与长英质矿物及磁黄铁矿、黄铜矿等金属硫化物密切共生。为确定黄羊山石墨矿床的成因和成矿物质来源,本文开展了球状矿石中的石墨拉曼光谱分析和C同位素测试,对与石墨密切共生的金属硫化物开展S-Pb同位素分析。结果表明,黄羊山矿床球状矿石不同部位石墨的拉曼谱峰相似,显示具有很高的结晶程度,估算结晶温度为750～800℃;7件石墨样品的δ~(13)C值在-19.27‰～-19.90‰,分布非常集中,介于岩浆碳值和有机碳值之间,表明具有两者的混合来源。4件磁黄铁矿样品的δ~(34)S值集中在-2.3‰～-2.9‰之间,接近原始地幔值;在Pb同位素构造环境判别图解上,Pb同位素比值(~(206)Pb/~(204) Pb=18.114～19.040,~(207)Pb/~(204) Pb=15.448 ～ 15.543,~(208) Pb/~(204)Pb=38.253～38.915)显示较好的线性关系,延伸方向与地幔演化曲线的延伸方向基本一致;S-Pb同位素测试结果表明,与石墨共生金属硫化物具有幔源特征。综合黄羊山矿床成矿地质条件、成矿特征、石墨及共生硫化物的物质来源等研究结果,本文初步认为,黄羊山石墨矿床形成于碱性花岗岩的岩浆作用阶段,矿石中的金属硫化物来自岩浆混合作用中的幔源基性端元,碳质由于岩浆同化混染作用达到饱和,在硫化物的催化下沉积形成石墨。  相似文献   

青藏高原西部阿汝冰芯记录的近100 a气温变化研究   总被引：2，自引：2，他引：0  

杨丹丹  姚檀栋  邬光剑  朱美林  德吉 《冰川冻土》2021,43(1):124-134

以2017年9月钻取自青藏高原西部阿汝冰崩区长度55.29 m的阿汝冰芯为研究对象,通过冰芯δ¹⁸O记录与Nye模型重建了冰芯上部17.87 m的时间序列是1917—2016年。结合冰芯邻近的改则、狮泉河气象站1973—2016年夏季平均气温数据,通过相关性分析及线性回归法、Mann-Kendall（M-K）检验分析,发现冰芯与气象站记录的过去44年气温显著升高;根据M-K突变检验得出,20世纪80年代是气温变化由高—低—高的转折时期,且阿汝冰芯记录的突变年份1981年前后气温上升约1.97 ℃。同样地,采用线性回归法、M-K检验分析阿汝冰芯与邻近的古里雅冰芯共同记录的1917—1991年气温变化情况,发现两支冰芯记录的75年间气温变化总体呈上升趋势;根据M-K突变检验得出,升温始于20世纪30年代中后期并于50年代达到显著升温的趋势,且阿汝冰芯记录的突变年份1949年前后气温上升了约1.1 ℃。阿汝冰芯与气象站和古里雅冰芯记录的气温变化具有一致的升温趋势,但阿汝冰芯记录的增温幅度比气象站记录高,同时比古里雅冰芯记录的增温幅度小。  相似文献   

运用H、O同位素分析石阡地区地热水来源     

李永康  陈正山  王甘露 《水文》2021,41(1):28-34

通过对贵州省石阡地区地热水、冷泉及河流的地热地质条件、水化学成分及氢氧同位素分析,对该地区的地热水、冷泉及河流的水化学特征、来源及石阡地区的补给模式进行了研究。温泉水属于低中矿化度的弱碱性水;温泉群中阳离子以Ca^2+、Mg^2+为主,阴离子以SO4^2-和HCO3^-为主,研究区水化学类型主要为HCO3-Ca和SO4.HCO3-Ca型。区域内地热水中δ18O值为-9.32‰~-6.81‰,δD为-64.4‰~-44.9‰;冷泉及河流中δ18O值为-7.51‰~-6.00‰,δD为-50.7‰~-38.2‰,均分布在我国大气降水线及当地大气降水线附近,表明该地区主要是大气降水成因。通过H、O同位素计算补给区温度,地热水补给高程,以及冷泉及河流补给高程,推测出补给区可能为袍木寨背斜一带及红石走滑断裂及其断裂束附近的碳酸盐岩裸露地区。氚盈余参数d表明石阡地区大多数地热水埋深较浅,循环径流时间较短,地质环境处于开放与半开放之间,水-岩反应作用相对较弱。  相似文献   

哀牢山中段镇沅金矿晚二叠世花岗斑岩U-Pb年代学、岩石地球化学及其构造意义     

张垚垚  张达  陈宣华  莫宣学  赵泽南  霍海龙 《岩石学报》2021,37(6):1674-1690

云南镇沅地区位于哀牢山构造带中段,是古特提斯哀牢山洋关闭及碰撞造山的关键部位。本文对该地区出露的花岗斑岩进行了年代学、岩石地球化学与同位素地球化学研究。锆石U-Pb年代学给出加权平均年龄为253.3±2.0Ma,表明花岗斑岩形成于晚二叠世。3个花岗斑岩脉共5个样品分析结果表明,其SiO_2含量65.30%～70.79%,全碱含量(K_2O+Na_2O)3.53%～4.39%,Al_2O_3含量13.42%～16.40%,为高钾钙碱性亚碱性系列岩石,成分上与花岗闪长岩类似,为S型花岗岩。稀土元素含量较低,轻重稀土分异程度较高,稀土配分曲线为右倾,无明显Ce异常,具弱负Eu异常,微量元素配分曲线为右倾,大离子亲石元素相对富集,高场强元素相对亏损,与典型地壳相一致。锆石Hf同位素ε_(Hf)(t)为-1.0～4.1,显示岩浆源区为亏损地幔和古老地壳物质部分熔融。岩石大地构造环境分析表明,该花岗斑岩形成于晚二叠世同碰撞构造环境。  相似文献   

Effect of the Dry Ashing Method on Cadmium Isotope Measurements in Soil and Plant Samples     

Wei‐Xin Lv  Hao‐Ming Yin  Meng‐Shu Liu  Fang Huang  Hui‐Min Yu 《Geostandards and Geoanalytical Research》2021,45(1):245-256

A dry ashing method is commonly used to remove organic material from samples prior to geochemical analysis. In the course of this study, the Cd isotope ratios of a series of soil and plant reference materials and samples were studied to evaluate the effect of the dry ashing method on measurement results of Cd isotope ratios. The samples were pre‐treated using the dry ashing method and high‐pressure bomb for comparison. The results show that the digestion using high‐pressure bombs did not lead to Cd loss, but using the dry ashing method would cause different proportions of Cd loss. The whole range of Cd isotope difference between two methods was from ?0.07‰ to 3.01‰. There was also an obvious difference in measured Cd isotope ratios from the same leaf sample pre‐treated independently by the dry ashing method, indicating that the amount of Cd loss and the effect on Cd isotope measurement during dry ashing is related to the properties of the samples. Therefore, dry ashing may not be appropriate for the removal of organic material in Cd isotope ratio measurement, especially for samples with high organic contents. The δ^114/110Cd values of reference materials NIST SRM 1573a and GSD‐30 are reported for the first time in this study.  相似文献   

Inter‐laboratory Characterisation of Apatite Reference Materials for Chlorine Isotope Analysis     

Alicja Wudarska  Ewa S&#x;aby  Michael Wiedenbeck  Jaime D. Barnes  Magali Bonifacie  Neil C. Sturchio  Grard Bardoux  Frdric Couffignal  Johannes Glodny  Linnea Heraty  Timm John  Christof Kusebauch  Sathish Mayanna  Franziska D. H. Wilke  Ewa Deput 《Geostandards and Geoanalytical Research》2021,45(1):121-142

Here we report on a set of six apatite reference materials (chlorapatites MGMH#133648, TUBAF#38 and fluorapatites MGMH#128441A, TUBAF#37, 40, 50) which we have characterised for their chlorine isotope ratios; these RMs span a range of Cl mass fractions within the apatite Ca₁₀(PO₄)₆(F,Cl,OH)₂ solid solution series. Numerous apatite specimens, obtained from mineralogical collections, were initially screened for ³⁷Cl/³⁵Cl homogeneity using SIMS followed by δ³⁷Cl characterisation by gas source mass spectrometry using both dual‐inlet and continuous‐flow modes. We also report major and key trace element compositions as determined by EPMA. The repeatability of our SIMS results was better than ± 0.10‰ (1s) for the five samples with > 0.5 % m/m Cl and ± 0.19‰ (1s) for the low Cl abundance material (0.27% m/m). We also observed a small, but significant crystal orientation effect of 0.38‰ between the mean ³⁷Cl/³⁵Cl ratios measured on three oriented apatite fragments. Furthermore, the results of GS‐IRMS analyses show small but systematic offset of δ³⁷Cl_SMOC values between the three laboratories. Nonetheless, all studied samples have comparable chlorine isotope compositions, with mean 10³δ³⁷Cl_SMOC values between +0.09 and +0.42 and in all cases with 1s ≤ ± 0.25.  相似文献