150ka B.P.以来萨拉乌苏河流域的CaCO3旋回

以米浪沟湾地层剖面作为萨拉乌苏河流域的典型剖面，探讨了150kaB.P.以来的CaCO3含量分布与气候变化的关系。1）该剖面CaCO3含量及其低-高变化同古风成沙与上覆河湖相或古土壤构成的没积旋回呈现出明显的对应关系。与米浪沟湾剖面的沉积旋回一样，CaCO3在分布上相应地构成了27个含量高低变化旋回。2)CaCO3在风成沙中含量的分布比较稀散，0.8%-7.18%，平均值2.50%；在河湖相和古土壤中土壤中相对富集，2.20%-14.90%，平均值5.74%。从而揭示出其时两者的气候背景是不同的，前者是干旱寒冷气候作用下的风力的侵蚀、搬运与堆积的产物；而后者则与暖湿气候环境下萨拉乌苏河流域地处鄂尔多斯高原和黄土高原这间特殊的低洼地貌位置有关。气候暖湿，河湖沼泽发育、成土成壤作用增强，低洼的集水条件有利于CaCO3的聚集。3）导致米浪沟湾剖面CaCO3的多旋回相对稀钐与聚集的根本原因可能是150kaB.P.以来北半球冰期-间冰期气候波动影响下乌素沙漠冬夏季风的多次更迭所致。     

The Origin and Distribution of Salts on Alluvial Fans in The Atacama Desert,Northern Chile

The Atacama Desert has been predominantly hyperarid since the middle Miocene. Combined ionic and X-ray diffraction analysis shows that calcium sulphate is prevalent on three similar alluvial fans in salar basins across a transect of different environments in Antofagasta Province, northern Chile. Differences between the fans were largely due to the effect of local factors on salt input, secondary redistribution and deposit preservation. Thus carbonate was notable in the High Andes (fan C) and Pre-Cordillera (fan B), whereas in the Central Valley (fan A) greater qualities of the more soluble salts (chlorides and nitrates) probably reflect the higher level of aridity and an oceanic source (the camanchaca). Calcium sulphate distribution on the alluvial fans and on adjacent hilltops indicates an aeolian origin. Evidence from the Pre-Cordillera (fan B), however, suggests that salt input may have been episodic, related to changes in conditions within the general aridity and possibly to stone pavement and soil development. Calcium sulphate sources range from an input in Andean precipitation and the camanchaca to abundant regional evaporite deposits. It is probable, however, that products of Andean volcanism constitute the dominant primary source of calcium sulphate, and that the salt has subsequently been distributed widely within the endoreic basins of the region by a combination of groundwater, surface flow and the wind. © 1997 John Wiley & Sons, Ltd.     

Comparison of methods for calculating annual solute exports from six forested appalachian watersheds

Six methods were compared for calculating annual stream exports of sulfate, nitrate, calcium, magnesium and aluminum from six small Appalachian watersheds. Approximately 250–400 stream samples and concurrent stream flow measurements were collected during baseflows and storm flows for the 1989 water year at five Pennsylvania watersheds and during the 1989–1992 water years at a West Virginia watershed. Continuous stream flow records were also collected at each watershed. Solute exports were calculated from the complete data set using six different scenarios ranging from instantaneous monthly measurements of stream chemistry and stream flow, to intensive monitoring of storm flow events and multiple regression equations. The results for five of the methods were compared with the regression method because statistically significant models were developed and the regression equations allowed for prediction of solute concentrations during unsampled storm flows. Results indicated that continuous stream flow measurement was critical to producing exports within 10% of regression estimates. For solutes whose concentrations were not correlated strongly with stream flow, weekly grab samples combined with continuous records of stream flow were sufficient to produce export estimates within 10% of the regression method. For solutes whose concentrations were correlated strongly with stream flow, more intensive sampling during storm flows or the use of multiple regression equations were the most appropriate methods, especially for watersheds where stream flows changed most quickly. Concentration–stream flow relationships, stream hydrological response, available resources and required level of accuracy of chemical budgets should be considered when choosing a method for calculating solute exports. © 1997 John Wiley & Sons, Ltd.     

Cyclic fluctuations of anoxia during Cretaceous time in the South Atlantic Ocean

The holes of the DSDP-IPOD program in the South Atlantic Ocean document two major anoxic events during Oxfordian to middle Albian times and secondly from late Cenomanian to Santonian times. The black shales formed during these two anoxic events differ in their rhythmicity and origin.During Lower Cretaceous time, the anoxic conditions resulted from the confined, euxinic nature of the basins. The rhythmicity of these black shales probably does not result from a global phenomenon (climatic or tectono-eustatic), but from local conditions resulting from the slender dimensions of the young ocean basin(s). The diversity and the diachroneity of the deposits from the south to the north precisely reflect the dynamics of the oceanic spreading.During Upper Cretaceous time, the anoxic conditions fluctuated in relation to a mid-water oxygen-minimum zone. The rhythmicity of black shale deposition seems to result from a global phenomenon, because of the widespread occurrence of the event. In the South Atlantic ocean, the cyclic fluctuations of anoxia were due to cyclic variations in the depth of the mid-water oxygen-minimum zone. There is no simple process to explain such rhythmicity. It probably results from the interplay of the three main variables which characterize the oceans at the time of the Cenomanian-Turonian boundary: the increased rate of sea floor spreading, high sea-levels and low water-circulation.     

赤道东经90°海岭活塞柱状心钙同位素曲线特征及其古环境意义

A δ~(44) Ca curve from shells of the planktonic foraminifera Globigerinoides sacculifer in calcareous biogenic oozes has been extracted from the Nintyeast Ridge in the Indian Ocean since 300 ka. By combining terrigenous inputs(e.g., grain size, magnetic susceptibility, and turbidite frequency) with the oceanic productivity(e.g., biogenic content and Neogloboquadrina dutertrei content), it is found that the curve's variations are closely related to the historical evolution of the oceanic calcium cycle. The δ~(44)Ca value is in lower tendency and has small oscillation during Marine Isotope Stage(MIS) 6, when the supply of terrigenous detrital is highest. In contrast, during MIS 3,5 and 7, the δ~(44) Ca values are in higher tendency, and their fluctuations are consistent with the variations of the productivity proxies. These results suggest that the calcium isotopes are mainly influenced by the input of the Himalayan erosion products to the northern Indian Ocean. In addition, the developmental stages of calcareous planktons may have a secondary impact on the fluctuations of the calcium isotope ratio of sea water.     

CaZrO_3的性质及其在耐火材料中的应用

随着钢水的优质化,对有关的耐火材料提出了更高的要求,特别是耐火材料不能对钢水造成污染的要求。ＣａＯ耐火材料不仅不污染钢水且能捕获钢液中的氧化物夹杂物,具有净化钢水的作用［１］。然而ＣａＯ在空气中极易水化,故其使用受到限制。尽管各种防止ＣａＯ水化的技术不断有所发展［２］,但水化仍不可避免。不少研究在不破坏ＣａＯ性质的前提下,采用稳定的化合物形式,获得很好的效果。在ＣａＯ的化合物中,作为耐火材料使用最成功的是ＣａＯ与ＺｒＯ２的化合物ＣａＺｒＯ３［３］。它具有很好的抗水化性能,熔点也很高。在连铸温度下…     

喀斯特水库水化学特征及对无机碳沉积通量的指示

为探究筑坝后不同水库物理、化学、生物过程对水化学和碳循环的影响,本研究对贵州三岔河流域的平寨水库、普定水库以及猫跳河流域的红枫湖水库进行研究,于2018年3月2019年1月分别在入库河流和库区采集了分层水样和沉降颗粒物,并探究水中主要离子及颗粒物通量的时空变化特征及其控制因素.结果表明,水体主要离子的主要来源受碳酸盐溶解影响,并且离子浓度受光合作用控制.红枫湖水库水体水化学类型为Ca-Mg-HCO₃-SO₄型,普定水库、平寨水库水化学类型均为Ca-HCO₃-SO₄.夏季藻类光合作用诱导碳酸盐沉淀导致水体表层Ca²⁺、HCO₃^-及溶解态Si浓度降低,其降低幅度分别为20.87%~44.25%、33.12%~51.18%、48.55%~96.34%.此外,藻类光合作用也影响C、N、Si等生源要素间的化学计量关系.Mg²⁺/Ca²⁺比值在水体垂向剖面上主要受碳酸钙沉淀的控制,而在不同水库之间则主要受流域岩性的控制.根据沉积物捕获器通量计算的平寨水库、普定水库、红枫湖水库夏季颗粒无机碳沉积通量分别为0.74、1.36、0.27 t/（km²·d）,而根据水体Ca²⁺浓度降低计算的通量分别为0.31~0.64、0.35~0.99、0.09~0.29 t/（km²·d）,根据水体HCO₃^-浓度降低计算的通量分别为0.30~0.65、0.29~1.26、0.12~0.33 t/（km²·d）.其红枫湖水库无机碳沉降通量的实测值与计算值接近,而平寨、普定水库实际沉降通量高于计算值,这可能是有外源输入导致.因此,利用水化学分层数据能对喀斯特水库中的无机碳沉降通量进行合理估算,并且能够得到较好的估算结果,从而指示碳循环的过程.     

偏高岭土协同石灰钝化红黏土水敏性的机制

红黏土水敏性强,添加石灰等碱性材料处治后,能获得即刻的改良效果,但由于红黏土呈弱酸性,石灰改良后其长期性能会衰减。为提高石灰稳定红黏土（简称La+L）的长期性能,添加偏高岭土（4%）协同石灰（5%）稳定红黏土（简称La+L+MK）,改善其水敏性和酸?碱互损作用。制备8种初始含水率的压实试样（初始孔隙比相同）,养护到预定时间后开展无侧限抗压强度试验,同时,测定试样的钙离子浓度、电导率和pH值。结果表明：初始含水率为26%左右时,改良土的无侧限抗压强度最高,初始含水率偏高或偏低都不利于改良土的强度增长。究其原因,试样偏干时,缺少水分,石灰水化不充分,不能形成游离态钙离子,无法进行火山灰反应,颗粒之间无法形成胶结;试样偏湿时,火山灰反应形成的胶结强度不及过量水分引起的基质吸力丧失量。试样的钙离子浓度和电导率变化规律,证实了以上原因解释的猜想。当然,添加偏高岭土后,能够显著改善偏湿状态下的石灰土强度。即使浸水饱和后,相对石灰改良土,也能够保持较高的强度,充分证明偏高岭土能够有效降低石灰土水敏性,提高其耐久性。偏高岭土直接提供了大量硅、铝氧化物,且将土体pH值降到有利于硅、铝氧化物溶解的碱性范围,加速火山灰反应,缓减或抑制石灰?红黏土的互损作用。     

NanoSr – A New Carbonate Microanalytical Reference Material for In Situ Strontium Isotope Analysis

The in situ measurement of Sr isotopes in carbonates by MC‐ICP‐MS is limited by the availability of suitable microanalytical reference materials (RMs), which match the samples of interest. Whereas several well‐characterised carbonate reference materials for Sr mass fractions > 1000 µg g^?1 are available, there is a lack of well‐characterised carbonate microanalytical RMs with lower Sr mass fractions. Here, we present a new synthetic carbonate nanopowder RM with a Sr mass fraction of ca. 500 µg g^?1 suitable for microanalytical Sr isotope research (‘NanoSr’). NanoSr was analysed by both solution‐based and in situ techniques. Element mass fractions were determined using EPMA (Ca mass fraction), as well as laser ablation and solution ICP‐MS in different laboratories. The ⁸⁷Sr/⁸⁶Sr ratio was determined by well‐established bulk methods for Sr isotope measurements and is 0.70756 ± 0.00003 (2s). The Sr isotope microhomogeneity of the material was determined by LA‐MC‐ICP‐MS, which resulted in ⁸⁷Sr/⁸⁶Sr ratios of 0.70753 ± 0.00007 (2s) and 0.70757 ± 0.00006 (2s), respectively, in agreement with the solution data within uncertainties. Thus, this new reference material is well suited to monitor and correct microanalytical Sr isotope measurements of low‐Sr, low‐REE carbonate samples. NanoSr is available from the corresponding author.     

南海西沙海槽83PC柱状沉积物组成特征及其古环境意义

为了解南海北部末次间冰期以来的沉积环境演化,分析了西沙海槽83PC柱状沉积物的浮游有孔虫氧碳同位素、碳酸钙、有机碳和粒度组成。浮游有孔虫的δ18 O值具有冰期-间冰期旋回特征,记录了海平面的升降和古气候的变化,而海平面变化控制了沉积物的碳酸钙和有机碳含量。冰期,海平面下降,陆源物质输入增多,带来了大量的碎屑物质和陆源有机质,沉积物具有低碳酸钙含量和高有机碳含量;间冰期,海平面上升,陆源物质输入减少,碎屑物质的稀释作用减弱,沉积物具有高碳酸钙含量和低有机碳含量。南海北部83PC柱状沉积物记录了末次间冰期以来的多次海平面升降旋回,还记录了气候变冷事件以及低碳酸钙沉积事件,其中,150、510、660和740cm处的低碳酸钙含量和相对重δ18 O值记录了全球性气候变冷事件,而冰后期的低碳酸钙沉积事件,则主要反映了季风降雨的增强,出现了洪水高发期,陆源碎屑物质对碳酸钙沉积的稀释作用明显增强。