两级磨料新型孕镶金刚石钻头

研制出一种两级磨料新型孕镶金刚石钻头,该种钻头解决了时效与寿命不能同步提高这一长期困扰钻头研制者的难题。现场应用证实了这种新型钻头的优越性,钻头综合指标较一般钻头提高１７９％。     

Chemistry of high mountain lakes in siliceous chatchments of the Central Eastern Alps

Alpine lakes in siliceous catchments of Tyrol and Carinthia (Austria) show signs of acidification. About 9% of the studied lakes have no alkalinity, more than 20% are below pH 6. About two thirds of all lakes have acid neutralizing capacities below 100 eq 1^–1. In spite of moderate precipitation acidity, some lakes show considerable concentrations of dissolved reactive aluminum during or shortly after snowmelt. High altitude lakes of the Alps are definitely more acidic than high mountain lakes in remote areas. Large differences in water and soil chemistry of nearby situated lakes were attributed to heterogeneities of bedrock geology. Paleolimnological investigations on former pH values of five lakes, based on diatom assemblages in the sediment, showed different developments: recent and past acidification, stable conditions, and alkalinization.     

Carbonate alteration of the Upper Mount McRae Shale beneath the martite-microplaty hematite ore deposit at Mount Whaleback, Western Australia

The formation of large martite-microplaty hematite ore deposits in northwest Australia remains a contentious topic in part because important evidence supporting a unifying genetic model has not been observed at all deposits. Carbonate replacement of silica has been found along normal faults below ore at the Mount Tom Price and Giles Mini deposits, which suggests an early hypogene process during ore formation. However, such rocks have not been identified at the largest martite-microplaty hematite deposit, Mount Whaleback. In this study, samples of the Mount McRae Shale are examined for their chemistry, mineralogy and petrography. These samples were collected from several key locations, including an area that immediately underlies ore along the Mount Whaleback fault at Mount Whaleback. Compared to unaltered black Mount McRae Shale from Wittenoom Gorge in the north and altered black and red Mount McRae Shale at Mount Whaleback, reddish-green Mount McRae Shale along the Mount Whaleback fault is greatly enriched in MgO and CaO and depleted in SiO₂. This chemistry arises from significant amounts of fine- to medium-grained ferroan-dolomite and ankerite and cross-cutting chlorite and carbonate veins. The composition is distinct from that produced during regional metamorphism, and most likely represents hydrothermal alteration after metamorphism. The lack of carbonate-rich, silica-poor rocks in the overlying Dales Gorge Member at Mount Whaleback is consistent with pervasive oxidation of most rocks in the region during or after ore genesis, a process that removed carbonates. Although several questions remain unanswered, these results support models that invoke an early hypogene stage during the formation of the martite-microplaty hematite deposits in the Hamersley Province.Editorial Handling: B. Lehmann     

方石英的亚稳态形成机制探讨

方石英形成于石英或鳞石英热力学稳定区是一种普遍的现象，并基本上是由非晶态SiO2转变而成。方石英的这种亚稳态形成机制可用Ostwald分步规则这一动力学经验规律来阐述；而引起非晶态SiO2转变成方石英的速率常数大大高于方石英转变成石英或鳞石英的速率常数的本质是非晶态SiO2局部中程有序结构与β—方石英的动态无序结构的相似性；这种相似性使非晶态SiO2结晶过程中β—方石英的有效成核速率大大增加，并最终导致亚稳态方石英的形成。非晶态SiO2中所含的杂质元素有利于降低方石英的形成温度，加速反应进程，但对于亚稳态方石英的形成没有决定作用，除非这些杂质元素有利于方石英结构的稳定性。     

硅胶／壳聚糖吸附材料的制备及表征

利用γ-氨基丙基-三乙氧基硅烷偶联剂与活化硅胶表面的羟基反应,制备了硅烷化硅胶,所得产物与壳聚糖反应合成了硅胶／壳聚糖复合吸附材料。通过红外光谱分析（IR）,扫描电镜（SEM）及能谱分析对复合材料进行表征,并测试了硅胶／壳聚糖复合材料对Zn^2＋、Cd^2＋的吸附能力。结果表明：复合吸附材料对Zn^2＋、Cd^2＋具有很好的吸附能力,最大吸附率为96．01％及90．65％。     

海洋沉积物32 Si测年方法研究

天然32Si是宇宙射线成因的,随着降水进入湖泊或海洋,被硅质生物摄取后最终存在于生物硅中。32Si来源单一,生产速率相对恒定,半衰期为150 a,可测年的时间尺度为100~1 000 a,是该时间尺度最合适的测年核素,填补了百年到千年时间尺度测年方法的空白。本文建立了海洋沉积物32Si的测量方法,主要步骤为:（1）样品前处理;（2）生物硅的分离与纯化;（3）生物硅样品中磷的分离与纯化;（4）32P的制样与β计数测量。全程通过硅钼蓝和磷钼蓝分光光度法监测实验过程硅和磷的损失情况,对南沙海域采集的沉积物岩心进行研究,得到南沙海域沉积物岩心32Si的平均活度为16.60 mBq/kg,范围值为8.39~33.34 mBq/kg;32Si在SiO₂中的平均比活度为0.356 Bq/kg,32Si的核素丰度平均值为1.29×10-16（32Si/SiO₂）;根据岩心32Si活度估算得深水区（水深1 335~1 537 m）和浅水区（121~141 m）岩心的沉积速率分别为0.106 cm/a、0.191 cm/a;根据32Si活度计算32Si的平均沉降通量为2.14×10-6 Bq/（cm2·a）,与参考文献的结果较为吻合。     

东印度洋近20 ka以来的生物硅记录及其古生产力意义

通过对东印度洋钻孔CJ01-185的生物硅来探讨东印度洋古生产力的变化和古气候演化的响应。CJ01-185钻孔的生物硅含量在末次冰期最低,为0.86%;而到了全新世晚期生物硅含量达到1.89%。全新世晚期生物硅的堆积速率明显大于末次冰期。随着全新世海平面的快速上升,巽他海峡贯通,来自爪哇海的陆源物质输入到东印度洋,导致全新世的生物硅含量和生物硅的堆积速率增加。研究表明：巽他海峡贯通前,研究区的古生产力主要受东南季风变化和上升流的活动影响;而巽他海峡贯通后,古生产力很明显受到陆源物质输入的控制,东南季风变化和上升流的影响较弱。     

南黄海生物硅的时空变化

Concentrations of biogenic silica(BSi) in the southern Yellow Sea were determined during four cruises(spring:April–May 2014; autumn: November 2014; summer: August–September 2015; winter: January 2016). Samples of BSi were measured using the double extraction method. Seasonal and spatial variations of BSi and the potential correlation between chlorophyll a(Chl a) content and BSi in four seasons were measured in this study. Significant spatial variability was observed in seawater BSi concentrations. The average concentration of BSi was highest in winter and lowest in spring. Furthermore, the relationships between concentrations of BSi and hydrological parameters were also discussed. There was a significant positive correlation between Chl a and BSi. The concentrations of BSi showed significant relationships with temperature and the concentrations of silicates, total inorganic nitrogen and total inorganic phosphorus, indicating that distribution of BSi was affected by temperature and nutrient level.     

西太平洋马尔库斯-威克海山区沉积物中生物硅含量分布

分析了大洋40航次在西太平洋马尔库斯-威克海山区山间海盆采集的表层沉积物中生物硅和有机质的含量,并对其分布特征和来源进行了初步的研究。结果表明,马尔库斯-威克海山区附近海域深海表层沉积物中生物硅含量总体较低,含量在0.88%～12.41%之间,平均含量为2.19%,分布上呈现西南含量高,向东北方向递减的趋势;深海表层沉积物中有机碳含量较低,δ¹³C同位素组成分布与生物硅相同。沉积物柱状样的研究表明研究区在过去的100～200 ka期间表层水体中硅质生物的初级生产力是逐渐增加的。     

Phosphorites,glass ramps and carbonate factories: The evolution of an epicontinental sea and a late Palaeozoic upwelling system (Phosphoria Rock Complex)

The Permian Phosphoria Rock Complex of the western USA contains an enigmatic assemblage of bioelemental rocks (i.e. phosphorites and cherts) that accumulated in a depositional system with no modern analogue. This study utilizes detailed sedimentological, stratigraphic and petrographic examination to evaluate the genetic relations of phosphorites, spiculitic chert and carbonates of the Ervay cycle (depositional sequence) and propose a unified oceanographic model for their deposition. The Ervay cycle contains three marine and one terrestrial facies association, each of which composes the bulk of a single lithostratigraphic unit. The marine facies associations include: (i) granular phosphorites (Retort Member); (ii) spiculitic cherty dolostones (Tosi Member); and (iii) marine to peritidal carbonates (Ervay Member). Red beds and intercalated gypsum (Goose Egg Formation) accumulated in the vast desert adjacent to the sea. The three marine members are chronostratigraphically distinct, successive and conformably stacked. They are not coeval facies belts. They reflect the progressive evolution of the epicontinental sea from the location of: (i) authigenic phosphogenesis (lowstand to transgression); to (ii) a glass ramp with biosiliceous (sponge) deposition (transgression); to (iii) a carbonate ramp (regression). This succession of switching biochemical sediment factories records the evolution of sea-level, nutrient supply, upwelling, oxygenation and dissolved Si. Intense upwelling, potentially coupled with aeolian input, led to sedimentary condensation and phosphogenesis. Decreased upwelling intensity during transgression increased oxygenation sufficiently for a siliceous sponge benthos. Sponges were favoured over biocalcifiers due to elevated dissolved silica and a low carbonate saturation state. The cessation of sponge dominance and transition to a carbonate ramp occurred due to decreasing upwelling intensity, Si drawdown and an increased carbonate saturation state. These results provide insight into the role of Si loading in faunal turnover on glass ramps and highlight how differences in dissolved Si utilizers in pre-Cretaceous versus post-Cretaceous upwelling systems influence the resultant deposits.