Theoretical calculation of equilibrium Mg isotope fractionation between silicate melt and its vapor

Isotope fractionation during the evaporation of silicate melt and condensation of vapor has been widely used to explain various isotope signals observed in lunar soils, cosmic spherules, calcium–aluminum-rich inclusions, and bulk compositions of planetary materials. During evaporation and condensation, the equilibrium isotope fractionation factor (α) between high-temperature silicate melt and vapor is a fundamental parameter that can constrain the melt’s isotopic compositions. However, equilibrium α is difficult to calibrate experimentally. Here we used Mg as an example and calculated equilibrium Mg isotope fractionation in MgSiO₃ and Mg₂SiO₄ melt–vapor systems based on first-principles molecular dynamics and the high-temperature approximation of the Bigeleisen–Mayer equation. We found that, at 2500 K, δ²⁵Mg values in the MgSiO₃ and Mg₂SiO₄ melts were 0.141?±?0.004 and 0.143?±?0.003‰ more positive than in their respective vapors. The corresponding δ²⁶Mg values were 0.270?±?0.008 and 0.274?±?0.006‰ more positive than in vapors, respectively. The general \(\alpha - T\) equations describing the equilibrium Mg α in MgSiO₃ and Mg₂SiO₄ melt–vapor systems were: \(\alpha_{{{\text{Mg}}\left( {\text{l}} \right) - {\text{Mg}}\left( {\text{g}} \right)}} = 1 + \frac{{5.264 \times 10^{5} }}{{T^{2} }}\left( {\frac{1}{m} - \frac{1}{{m^{\prime}}}} \right)\) and \(\alpha_{{{\text{Mg}}\left( {\text{l}} \right) - {\text{Mg}}\left( {\text{g}} \right)}} = 1 + \frac{{5.340 \times 10^{5} }}{{T^{2} }}\left( {\frac{1}{m} - \frac{1}{{m^{\prime}}}} \right)\), respectively, where m is the mass of light isotope ²⁴Mg and m′ is the mass of the heavier isotope, ²⁵Mg or ²⁶Mg. These results offer a necessary parameter for mechanistic understanding of Mg isotope fractionation during evaporation and condensation that commonly occurs during the early stages of planetary formation and evolution.     

Metallogeny of the Baiyangping Lead‐Zinc Polymetallic Ore Concentration Area,Northern Lanping Basin of Yunnan Province,China

The Lanping Basin in the Nujiang‐Lancangjiang‐Jinshajiang (the Sanjiang) area of northeastern margin of the Tibetan Plateau is an important part of eastern Tethyan metallogenic domain. This basin hosts a number of large unique sediment‐hosted Pb‐Zn polymetallic deposits or ore districts, such as the Baiyangping ore concentration area which is one of the representative ore district. The Baiyangping ore concentration area can be divided into the east and west ore belts, which were formed in a folded tectogene of the India‐Asia continental collisional setting and was controlled by a large reverse fault. Field observations reveal that the Mesozoic and Cenozoic sedimentary strata were outcropped in the mining area, and that the orebodies are obviously controlled by faults and hosted in sandstone and carbonate rocks. However, the ore‐forming elements in the east ore belt are mainly Pb‐Zn‐Sr‐Ag, while Pb‐Zn‐Ag‐Cu‐Co elements are dominant in the west ore belt. Comparative analysis of the C‐O‐Sr‐S‐Pb isotopic compositions suggest that both ore belts had a homogeneous carbon source, and the carbon in hydrothermal calcite is derived from the dissolution of carbonate rock strata; the ore‐forming fluids were originated from formation water and precipitate water, which belonged to basin brine fluid system; sulfur was from organic thermal chemical sulfate reduction and biological sulfate reduction; the metal mineralization material was from sedimentary strata and basement, but the difference of the material source of the basement and the strata and the superimposed mineralization of the west ore belt resulted in the difference of metallogenic elements between the eastern and western metallogenic belts. The Pb‐Zn mineralization age of both ore belts was contemporary and formed in the same metallogenetic event. Both thrust formed at the same time and occurred at the Early Oligocene, which is consistent with the age constrained by field geological relationship.     

山东黄金西岭勘查区深部勘探孔防斜与纠斜措施

西岭勘查区金矿找矿工作已全面进入勘探阶段,勘查区网度为80 m×80 m,对于钻孔质量要求十分严格：终孔靶点偏差不超过勘探网度的四分之一,即不超过20 m。对于西岭勘查区设计孔深均超过1500 m（部分钻孔设计甚至超过2500 m）的钻孔而言,这种要求远远超过地质岩心钻探规程要求。山东黄金地勘公司根据多年深孔施工经验,在防斜与纠斜方面均取得了一些突破,自主研发了钻具扶正器、独创了钻孔纠斜法,形成了一套实用的钻孔质量保证措施。     

三峡库岸滑坡变形特征及影响因素分析

三峡库区涉水滑坡主要影响因素是水位和降雨量,也是库区滑坡体失稳的主要影响因素和诱发因素。库区每年重复着水位升降不利于滑坡的稳定,而降雨特别是大强度的降雨也诱发产生滑坡。当水位波动遇到降雨,出现工况叠加,滑坡将加剧。因此,有必要对影响滑坡变形的主导因素进行了解分析。2016年6月三峡库区全面展开了自动化监测,使得数据统计方便可靠。本文采用滑坡变形速率、降雨量、库水位变化、最大水位变化速率、淹没程度,运用灰色关联度分析法对涉水滑坡进行了计算分析。水位下降阶段,文中土质滑坡变形受库水位影响最大。水位上升阶段,该土质滑坡上部变形受降雨影响最大,下部受水位影响最大。文中岩质滑坡总是受库水位影响最大。     

贵州松桃高地特大型富锰矿床主要地质特征

位于贵州铜仁松桃国家锰矿整装勘查区内的高地富锰矿床,(332)+(333)类碳酸锰富锰矿石资源量达7 166. 84万吨,锰平均品位25. 75%,矿体平均厚度4. 52 m,富锰矿体赋存于总资源量达1. 61亿吨的高地超大型锰矿床之中,由一个单一的富锰矿体构成,是我国新发现的首个特大型富锰矿床,富锰矿资源量相当于我国富锰矿资源量总和的2倍。成因类型属古天然气渗漏沉积型锰矿床,富锰矿产于古天然气渗漏沉积成矿系统中心相区。高地富锰矿床地处独特的"新月形"南华纪早期李家湾-高地-道坨(Ⅳ级)地堑盆地中心,菱锰矿体中均出现以块状构造夹被沥青充填的气泡状富菱锰矿石。地表燕山期北北东向的断裂构造十分发育,但主要为上陡下缓犁式正断层,未触及高地深部隐伏巨型锰矿体,以致富锰矿体保存亦十分完整,易于开发利用。     

基于遥感和GIS的岩溶区1∶5万区域地质填图难易程度分区

从岩溶区1∶5万区域地质填图的实际需求出发,采用遥感地质综合解译和GIS综合分析相结合的技术手段,在详细解译区域地质、地貌、环境、水文等要素的基础上,以地层延伸性、地形地势、水系形态、冲沟密度为评价参数,定性地划分了研究区1∶5万区域地质填图的难易程度。实地调查显示,区域地质填图难易程度分区的成果与研究区的实际地质情况基本一致,可作为岩溶区1∶5万区域地质填图工作部属的依据,能在保证成果精度的前提下显著提高岩溶区1∶5万区域地质调查的工作效率。      

围压和孔隙结构对不同粒级砂岩孔隙度渗透率的影响实验研究

孔隙度和渗透率是储层评价的两个重要参数.岩石毛管压力曲线和核磁共振T2谱图是描述储层微观结构特征的重要参数.通过测量不同压力条件下岩心样品的孔隙度和渗透率,得到了孔隙度和渗透率随压力的变化情况.实验结果表明：孔隙度和渗透率随着压力的增加而降低,并且与压力服从对数函数变化规律.不同孔隙度渗透率区间的砂岩样品,孔隙度和渗透率随着压力变化的趋势不同.通过测量不同粒级砂岩样品的毛管压力曲线和核磁共振T2谱图,证实了孔隙结构对孔隙度和渗透率的影响,微观孔隙结构是决定渗透性好坏的关键因素.     

辽宁凌源四合当地区九佛堂组珍稀化石层划分及意义

辽宁省凌源市四合当地区九佛堂组含有丰富的中生代热河生物群化石,尤其是珍稀化石.通过剖面测制、化石采集以及实地调查等手段,将九佛堂组划分为3个段,确定了化石层的分布及重要化石的产出层位,同时命名了3个化石层：一段的韩家沟层、二段的卅二道湾层、三段的四合当层,加深了辽西九佛堂组化石层的研究程度.     

内蒙古巴林右旗晚二叠世埃达克质火山岩特征及其地质意义

内蒙古东南部巴林右旗地区发育晚二叠世埃达克质火山岩,岩石组合为安山岩、粗安岩、英安岩及辉石安山岩,其LA-ICP-MS锆石U-Pb测年结果为256.7±2.7Ma,指示其形成于晚二叠世。地球化学特征显示,该套火山岩属准铝质-弱铝质中钾钙碱性岩石系列,具富Si(SiO_256%)、高Al(Al_2O_315%)、富Na、贫K、高Sr、低Yb和Y等特征,Na_2O/K_2O值为2.33~3.90,Mg~#值为35.3~60.8;稀土元素总量为96.69×10~(-6)~192.4×10~(-6)、轻重稀土元素分馏较明显((La/Yb)_N值为6.27~13.82),具正的Eu(δEu=1~1.67)异常,在原始地幔标准化蛛网图中,富集大离子亲石元素Rb、Ba、U,亏损高场强元素Nb、Ta,为O型(大洋型)埃达克质火山岩地球化学特征。综合区域资料,巴林右旗埃达克质火山岩是残留在地幔中的古亚洲洋残余洋壳部分熔融并受到地幔橄榄岩混染形成的,暗示晚二叠世存在古亚洲洋向华北板块俯冲消亡事件。     

内蒙古1∶5万乌音呼日勒庙等四幅区域地质矿产调查新进展

内蒙古1∶5万乌音呼日勒庙等四幅区域地质矿产调查项目取得的新进展及主要成果为: 根据岩石组合、动植物化石及同位素年龄等,重新厘定、划分了16个岩石地层填图单位,在多个组段沉积岩层位中首次发现丰富的动、植物化石,建立了各地层年代学格架; 将侵入岩重新解体划分为4个填图单元,并建立了侵入岩年代学格架; 新发现1处规模较大的韧性变形带,主要为逆—左行走滑韧性断层,时代归属于中三叠世末期,为额尔古纳河—阿龙山NE向韧性变形域的南部延伸; 新发现矿(化)点20处,其中金属矿点3处,金属矿化点6处,非金属矿点9处,非金属矿化点2处; 总结了该区成矿规律,圈定了成矿远景区及找矿靶区。