2000年—2020年中国大型湖泊月平均透明度遥感监测数据集

湖泊水体透明度是湖泊水环境状况的综合表征,与多种水质参数关系密切,对湖泊水环境监测具有重要意义.本文的目的 是介绍一种中国大型湖泊(＞20 km2)月平均透明度遥感监测数据集的生成流程、主要特征和应用价值.数据集生产方法是将Liu等(2020)构建的透明度遥感算法应用于GEE (Google Earth Engine)...     

海水热力学方程TEOS-10及其与海水状态方程EOS-80的比较

新的2010年海水热力学方程TEOS-10采用1990年国际温标以及考虑世界大洋海水组成空间差异的绝对盐度,与旧的1980年海水状态方程EOS-80相比,具有更高的准确度和更广的适用范围,能够直接计算包括熵、焓、热容量在内的旧方程无法计算的热力学变量,将给海洋学研究带来重要的影响。借助气候态平均数据计算的结果表明,新旧方程计算的密度之差,在全球大多数海域可超过10-2kg/m3。在赤道以北的太平洋和印度洋海域,包括中国东海和南海的深海区域,该差别尤为显著,在精度要求较高的研究中必须予以考虑。新方程对密度计算的这一修正主要归因于其首次提出的绝对盐度,考虑了包括中性溶质在内的所有溶质的作用,弥补了实用盐标的缺陷。新旧方程计算冰点等其他物理量也有相应的修正。应尽快推广应用TEOS-10以及绝对盐度,充分发挥其对海洋学发展的推动作用。     

中国三地软玉的矿物组成和成矿地质背景研究

为了查明新疆玛纳斯、青海格尔木、江苏溧阳产软玉的矿物组成和了解其品质与矿物组成的内在联系,为软玉的鉴别与质量评价等提供基础资料,采用偏光显微镜、电子探针、X射线粉末衍射等测试方法对3个产地的软玉样品进行了测试分析,从矿物成因特征、结构构造、矿物组成、化学成分等方面进行了对比分析。结果表明,新疆玛纳斯、青海格尔木、江苏溧阳的软玉虽然均由透闪石组成,但其晶体中Mg与Fe的离子数量明显不同,玛纳斯碧玉中的透闪石含有更多的Fe,其化学成分十分接近阳起石的;玛纳斯碧玉的成矿地质背景与格尔木和溧阳的有所差别,形成于蛇纹石化超镁铁岩中,富含FeOT和MgO,而溧阳和格尔木软玉则产于中酸性火成岩与白云质大理岩的接触带中,其FeOT的质量分数较低。软玉的颜色、韧性和透明度主要取决于其形成的地质背景条件。     

Possible link between new coronavirus variants and atmospheric lightning and seawater intrusion

自新型冠状病毒肺炎暴发一年多以来,已经对全球产生深远影响.新型冠状病毒肺炎变异毒株的出现使当前疫情发展充满了不确定性.从这方面出发,我们讨论病毒变异与大气因素之间的联系.根据固氮过程和硝酸盐在人体中的转化过程,我们提出了新型冠状病毒肺炎变异毒株的出现或许和闪电以及海水入侵有联系.我们的研究对新型冠状病毒肺炎变异毒株可能的产生原因提供新的观点.     

基于非均匀水体对比度传输方程的海水透明度计算试验

针对均匀水体假设的海水透明度经验计算公式不具有普适性的缺点,将海水在垂直方向上分为若干光学性质相近的均匀层,推导出非均匀水体中目标对比度传输方程,在此基础上,建立了海水透明度的计算模型。利用BROKE_WEST_ACS实测的海水固有光学性质数据和透明度盘观测数据,对计算模型进行了数值试验和效果分析。结果表明:模型计算值与透明度盘实测值平均相对误差为9.1%;该模型既克服了透明度盘测量易受天气状况和人眼差异影响较大的缺点,又突破了均匀水体透明度计算方法的局限性。     

三峡小江回水区透明度季节变化及其影响因子分析

三峡成库后其季节调蓄过程使该水域湖沼学特征具有独特性.根据三峡小江流域回水区段为期2年的定位跟踪观测,对透明度(SD)和主要环境指标的相互关系进行分析研究.研究期间,小江回水区透明度均值为170±7cm,各采样点透明度差异不明显且季节变化过程一致,自春末夏初开始降至最低水平,夏季汛期相对稳定,夏末入秋持续升高,冬季维持在较高状态,入春后下降.对透明度和主要环境指标的相关性分析发现,无机悬浮颗粒(PIM)是影响透明度的主要指标.透明度同PIM、Chl.a多元回归模型为:SD=(-89.389±8.101)·lg(PIM)+(-84.008±8.624)·lg(Chl.a)+(264.132±8.232).汛期低水位状态下(145-150m)小江回水区水动力条件趋于天然河道,河道输沙量增加使无机悬浮颗粒含量远高于藻类生物量而成为影响透明度的主要环境指标.在中水位(150-156m)和高水位(156m以上),虽然藻类进入非生长季节,但水位抬升和水体滞留时间的延长促使悬浮颗粒物大量沉淀,悬浮生长于表层水体的藻类成为影响透明度的主要环境指标,生物作用对透明度的影响明显.     

Seawater-like trace element signatures (REE + Y) of Eoarchaean chemical sedimentary rocks from southern West Greenland,and their corruption during high-grade metamorphism

Modern chemical sediments display a distinctive rare earth element + yttrium (REE + Y) pattern involving depleted LREE, positive La/La*_SN, Eu/Eu*_SN, and Y_SN anomalies (SN = shale normalised) that is related to precipitation from circumneutral to high pH waters with solution complexation of the REEs dominated by carbonate ions. This is often interpreted as reflecting precipitation from surface waters (usually marine). The oldest broadly accepted chemical sediments are c. 3,700 Ma amphibolite facies banded iron-formation (BIF) units in the Isua supracrustal belt, Greenland. Isua BIFs, including the BIF international reference material IF-G are generally considered to be seawater precipitates, and display these REE + Y patterns (Bolhar et al. in Earth Planet Sci Lett 222:43–60, 2004). Greenland Eoarchaean BIF metamorphosed up to granulite facies from several localities in the vicinity of Akilia (island), display REE + Y patterns identical to Isua BIF, consistent with an origin by chemical sedimentation from seawater and a paucity of clastic input. Furthermore, the much-debated magnetite-bearing siliceous unit of “earliest life” rocks (sample G91/26) from Akilia has the same REE + Y pattern. This suggests that sample G91/26 is also a chemical sediment, contrary to previous assertions (Bolhar et al. in Earth Planet Sci Lett 222:43–60, 2004), and including suggestions that the Akilia unit containing G91/26 consists entirely of silica-penetrated, metasomatised, mafic rock (Fedo and Whitehouse 2002a). Integration of our trace element data with those of Bolhar et al. (Earth Planet Sci Lett 222:43–60, 2004) demonstrates that Eoarchaean siliceous rocks in Greenland, with ages from 3.6 to 3.85 Ga, have diverse trace element signatures. There are now geographically-dispersed, widespread examples with Isua BIF-like REE + Y signatures, that are interpreted as chemically unaltered, albeit metamorphosed, chemical sediments. Other samples retain remnants of LREE depletion but are beginning to lose the distinct La, Eu and Y positive anomalies and are interpreted as metasomatised chemical sediments. Finally there are some siliceous samples with completely different trace element patterns that are interpreted as rocks of non-sedimentary origin, and include metasomatised mafic rocks. The positive La/La*_SN, Eu/Eu*_SN and Y_SN anomalies found in Isua BIFs and other Eoarchaean Greenland samples, such as G91/26 from Akilia, suggests that the processes of carbonate ion complexation controlling the REE − Y patterns were already established in the hydrosphere at the start of the sedimentary record 3,600–3,850 Ma ago. This is in accord with the presence of Eoarchaean siderite-bearing marbles of sedimentary origin, and suggests that CO₂ may have been a significant greenhouse gas at that time.     

Evolution of groundwater salinity in the unconfined aquifer of Bou-Areg, Northeastern Mediterranean coast, Morocco

The Bou-Areg plain in the Mediterranean coast at the North-eastern of Morocco is characterized by a semi-arid climate. The aquifer consists of two sedimentary formations of Plio-quaternary age: the upper formation of fine silts and the lower one of coarse silts with sand and gravels. The aquifer is underlain by marly bedrock of Miocene age that dips toward the coastal lagoon of Bou-Areg. The hydrodynamic characteristics vary between 10⁻⁴ and 10⁻³ m/s; and transmissivities range between 10⁻⁴ and 10⁻¹ m²/s. The general direction of flow is SW to NE, toward the lagoon. The aquifer is crossed by the river Selouane, which also ends in the lagoon. The groundwater is characterized by a high salinity that can reach 7.5 g/l. The highest values are observed in the upstream and in the downstream sectors of the aquifer. The temporal evolution of the physico-chemical parameters depends on the climatic conditions and piezometric variations. The analysis of the spatio-temporal distribution of the physico-chemical parameters suggests different sources of groundwater salinization: the seawater intrusion, the influence of marly gypsum-bearing terrains, and the influence of anthropogenic products as the agricultural fertilizers, which cause great nitrate concentrations that vary between 80 and 140 mg/l.     

正己烷/海水微乳液形成的相图研究

用相图方法研究正己烷／海水微乳液的形成。体系相图由水（或人工海水，盐度分别为０，１３．６９６，３０．０７０和４１．１１８）／油（正己烷）／表面活性剂（ＡＳ，ＣＴＡＢ及ＢＲＩＪ３５）／助表面活性剂（正丁醇）在４０℃时构成。分别研究表面活性剂类型，油及醇含量和海水盐度对微乳液形成的影响。结果表明：醇与表面活性剂的摩尔浓度比值大于１时，最适宜于形成微乳液；形成微乳液区的面积随正己烷含量增加而减少；含离子