中国内蒙古白云鄂博Fe—Nd—REE矿床地质特征与陨石撞击成因

中国内蒙古白云鄂博Ｆｅ－Ｎｂ－ＲＥＥ矿床由于其独特的矿床地质与矿物地球化学特征而明显有别于世界上其它绝大多数的Ｆｅ,Ｎｂ,ＲＥＥ矿床,本文提出该矿床是约１５００Ｍａ前一块富含ＲＥＥ,Ｎｂ的铁陨石撞击在华北地台北缘碳酸盐沉积陆架上形成的。现在矿床矿体中心的块状铁矿石更多地代表了陨石的成分,矿体外侧富含ＲＥＥ,Ｎｄ的环状白云岩是形成的含金属热液蚀变沉积成因方解石质碳酸盐沉积物的结果。     

冲绳海槽晚更新世以来环境演变的矿物-地球化学记录

国家自然科学基金资助项目（Ｎｏ．４９６７６２９０,１９９７～１９９９）“冲绳海槽晚更新世以来环境演变的矿物 地球化学记录” ,根据表层和柱状样品的成因矿物学和地球化学研究 ,重建了冲绳海槽中部自晚更新世以来的环境演变历史。沉积物的ＴｉＯ２ （ＴＦｅ２Ｏ３ ＭｇＯ）,Ｋ２Ｏ／Ｎａ２Ｏ （ＴＦｅ２Ｏ３ （ＴＦｅ２Ｏ３ ＭｇＯ）,Ａｌ／（Ａｌ Ｍｎ Ｆｅ）,Ｌａ／Ｙｂ ＲＥＥ,ＬＲＥＥ／ＨＲＥＥ（平均８．６９） ,δＥｕ（平均０．６０）和轻稀土型配分类型特征判明为活动大陆边缘 大陆岛弧型沉积环境 ,沉积物具有典型…     

陆缘南海成矿金属存在形式和沉析作用的定量研究

通过溶液化学平衡反应模型理论计算表明：软泥水和底层海水除Ｆｅ在软泥水中呈高价态的分子化合物（Ｆｅ（ＯＨ）３）和络合离子（Ｆｅ（ＯＨ）２＋）,以及二者均存在含量甚微的单一离子Ｆｅ３＋以外,Ｆｅ的其它组分形式和Ｍｎ、Ｃｕ、Ｎｉ、Ｃｏ元素均以低价态的单一离子、络合离子和分子化合物形式存在。软泥水比底层海水的组分存在形式要多,且组分含量变化幅度要大。软泥水中Ｆｅ主要含量是Ｆｅ（ＯＨ）３,而底层海水主要是Ｆｅ２＋。软泥水现代正在发生沉析的矿物有：赤铁矿、针铁矿和石英,在外陆架—陆坡海域软泥水可生成方解石、文石,陆坡海域的软泥水还可沉析菱锰矿和水锰矿;底层海水正在沉析的仅是方解石、文石、赤铁矿和针铁矿。碳酸盐类矿物的沉析与海底分布的钙质粘土、泥等沉积物相吻合。水锰矿的生成为陆坡海山区存在的多金属结壳（核）提供了成矿信息,并表明多金属结壳（核）不是通过海水的物理化学作用的途径生成的。     

O_2~(·-)损伤过氧化氢酶过程中辅基Fe(Ⅲ)的ESR波谱

在体外Ｏ·－２损伤ＣＡＴ的过程中,对ＣＡＴ辅基Ｆｅ（Ⅲ）的ＥＳＲ波谱进行了分析研究。发现：辅基Ｆｅ（Ⅲ）的ＥＳＲ谱线特征有显著改变,如：ｇ因子、ΔＨｐｐ及线型等均有显著变化。说明：辅基Ｆｅ（Ⅲ）的微观环境发生了变化,提示：这些变化可能是Ｏ·－２造成ＣＡＴ活性改变的主要分子机制。     

海坛岛海域表层沉积物中主量化学成分的地球化学

本文对海坛岛海域３３个表层沉积物中１０种化学成分的含量、含量变化和区域平面分布作了描述和探讨。化学成分中Ｃｏｒｇ、Ｎ、Ｐ、Ｆｅ、ＡＩ、Ｔｉ、Ｍｇ等元素的关性好,和粘土矿物关系密切,从陆源搬运入海;Ｃａ、碳酸盐和上述及粘土含量呈负相关,在富含生物介壳的粗粒沉积中富集;Ｍｎ主要赋存于陆源碎屑,而在砾砂中有自生Ｍｎ沉积。Ｑ型聚类分析的结果表明,调查区可分为３个地球化学分区,综合反映了沉积物的地球化学特征。     

南沙群岛珊湖礁潟湖垂直沉降颗粒物中主要元素的生物地球化学过程研究

本文首次报道用沉积物捕捉器（ＳＴ）研究南沙群岛珊瑚礁湖沉降颗粒物中主要元素垂直通量、垂直转移形态、再循环过程及垂直通量与表层海水温度的关系。结果显示,作为生物化学沉积标志的Ｃａ、Ｍｇ具有最高的垂直通量,达１．４和０．１ｇ／（ｍ２·ｄ）以上,作为生物富集标志的Ｂｒ、Ⅰ也有较高的垂直转移量;垂直转移形态的研究表明Ｎａ、Ｋ、Ｃａ、Ｍｇ、Ｓｒ主要以碳酸盐结合态向海底转移,其中Ｃａ、Ｍｇ、Ｓｒ占９９％以上,Ｆｅ、Ｉ、Ｂａ主要以铁锰氧化物结合态向海底输送,在垂直沉降颗粒物到达海底后,有相当部分的主要元素可再循环进入水体中,Ｂｒ、Ｉ、Ｋ、Ａｌ的绝大部分进入再循环,Ｍｇ、Ｎａ、Ｃｌ有一半左右进入再循环,Ｃａ、Ｓｒ、Ｂａ、Ｆｅ大部分被埋葬;Ｎａ等９种元素的垂直转移量随ＳＳＴ呈指数降低响应,对ＳＳＴ的敏感性Ｆｅ＞Ｂｒ＞Ｓｒ＞Ｃａ＞Ｎａ＞Ｃｌ＞Ｍｇ＞Ｉ＞Ａｌ,这再一次验证了ＣａＣＯ３随温度升高,其溶解度降低、化学沉积量增加这一自然界的普遍规律,表明在珊瑚礁海水的垂直沉降颗粒物中主要元素是作为珊瑚的重要成分与ＣａＣＯ３一同被沉积下来的,ＣａＣＯ３起到稀释剂的作用。     

海坛岛海域表层沉积物中主要化学成分的地球化学

本文对海坛岛海域３３个表层沉积物中１０种化学成分的含量、含量变化和区域平面分布作了描述和探讨。化学成分中Ｃｏｒｇ、Ｎ、Ｐ、Ｆｅ、Ａｌ、Ｔｉ、Ｍｇ等元素的相关性好,和粘土矿物关系密切,从陆源搬运入海;Ｃａ、碳酸盐和上述及粘土含量呈负相关,在富含生物介壳的粗粒沉积中富集;Ｍｎ主要赋存于陆源碎屑,而在砾砂中有自生Ｍｎ沉积。Ｑ型聚类分析的结果表明,调查区可分为３个地球化学分区,综合反映了沉积物的地球化学特     

REE distribution in water-sediment interface system at deep ocean floor

ＲＥＥｄｉｓｔｒｉｂｕｔｉｏｎｉｎｗａｔｅｒ－ｓｅｄｉｍｅｎｔｉｎｔｅｒｆａｃｅｓｙｓｔｅｍａｔｄｅｅｐｏｃｅａｎｆｌｏｏｒ￥ＺｈａｎｇＬｉｊｉｅ；ＬｉｕＪｉｈｕａａｎｄＹａｏＤｅ（ＲｅｃｅｉｖｅｄＦｅｂｒｕａｒｙ１，１９９４；ａｃｃｅｐｔｅｄＭａｙ...     

火星陨石ALH84001中碳酸盐高温成因的可能性

已被公认为火星来源的AllanHills陨石（ALH84001）因其含有大量带状、类似地表成因的碳酸盐矿物而有别于其它火星陨石．对这些碳酸盐矿物已有的氧同位素组成研究结果显示，它们似乎是形成于火星地壳中低温（0－80℃）水体中或者是近地表的热液体系中．本文报道了这些碳酸盐的主要元素组成分析结果，这些结果限制了它们形成时流体的温度和成分．我们认为对这些化学组成以及缺少共生的水成矿物的最好解释是，在一次撞击事件中，热的（＞650℃）富＊q流体与超基性宕反应形成了这些碳酸盐．火星陨石ALH84001主要由厘米大小、排成格架的等轴…     

约翰斯顿岛附近海域铁锰结壳矿物学和地球化学研究

铁锰结壳存在两种不同的产状，一种是铁锰氧化和的围绕“核心”生长形成的球状结壳，另一种是铁锰氧化物在基底岩石上生长形成的被状结壳。本文对Ｒ／Ｖ，Ｋａｉｍｉｋａｉ－Ｏ－Ｋａｎａｌｏａ船１９９３年１１月在约翰期顿岛附近海域取得铁锰结壳进行了矿物学和地球化学分析。该区铁锰结壳主要组成矿物为δ－ＭｎＯ２，Ｍｎ／Ｆｅ比值为２．０２，富Ｃｏ（０．８８１％），盆Ｃｕ（０．１％），稀土总量（∑ＲＥＥ）１９１８．２７     

中国鱼类名录Ⅻ--鳚亚目、(鱼衔)亚目、喉盘鱼亚目、鰕虎鱼亚目、微体鱼亚目、刺尾鱼亚目、带鱼亚目、鲭亚目、鲳亚目、金枪鱼亚目、攀鲈亚目、刺鳅亚目

鳚亚目 4 科 33 属 95 种，鰕虎鱼亚目 5 科 98 属 259 种，刺尾鱼亚目 5 科 11 属 65 种，鲈形目 19亚目 104 科 535 属 1799 种。     

The distribution of Mn,Fe, Cu,Ni, Co,Ga, Cr,V, Ba,Sr, Sn,Zn, and Pb,in some soil-sized particulates from the lower troposphere over the world ocean

Soil-sized particulates have been collected on board ship by a mesh technique from the lower troposphere of the North, Equatorial and South Atlantic Ocean, northern and southern Indian Ocean, South and East China Sea and various coastal localities.Spectrographic analysis reveals that, on average, the particulates have concentrations of Mn, Ni, Co, Ga, Cr, V, Ba, and Sr which are of the same order of magnitude as those in average crustal material. In contrast, the average concentrations of Pb, Sn, and Zn are one order of magnitude higher than those in average crustal material.Within this “world-wide” average there are significant geographical variations in the distributions of Pb, Sn, and Zn which may be related to anthropogenic sources.On the basis of trace-element distributions lower tropospheric soil-sized marine particulates have been divided into four genetic components; local, zonal, inter-zonal, and global. The proportions of these components vary geographically, and each component may have both a natural and an anthropogenic fraction.     

Distribution, abundance, and growth of larval tautog, Tautoga onitis, in Buzzards Bay, Massachusetts, USA

Tautog, Tautoga onitis, is an abundant species of fish in estuaries of the northeastern United States. Planktonic tautog larvae are abundant in summer in these estuaries, but there is little information on rates of growth of tautog larvae feeding on natural assemblages of food in the plankton. We examined abundance and growth of larval tautog and environmental factors during weekly sampling at three sites along a nearshore‐to‐offshore transect in Buzzards Bay, Massachusetts, USA during summer 1994. This is the first study of a robust sample size (336 larvae) to estimate growth rates of field‐caught planktonic tautog larvae feeding on natural diets, using the otolith daily‐growth‐increment method. The study was over the entire summer period when tautog larvae were in the plankton. The sampling sites contrasted in several environmental variables including temperature, dissolved oxygen (DO), and chlorophyll a concentration. There was a temporal progression in the abundance of tautog larvae over the summer, in relation to location and temperature. Tautog larvae were first present nearshore, with a pronounced peak in abundance occurring at the nearshore sites during the last 2 weeks in June. Larvae were absent at this time further offshore. From late June through August, larval abundance progressively decreased nearshore, but increased offshore although never approaching the abundance levels observed at the nearshore sites. The distribution and abundance of tautog larvae appeared to be related to a nearshore‐to‐offshore seasonal warming trend and a nearshore decrease in DO. Otoliths from 336 larvae ranging from 2.3 to 7.7 mm standard length had otolith increment counts ranging from 0 to 19 increments. Growth of larval tautog was estimated at 0.23 mm·day^?1, and length of larvae prior to first increment formation was estimated at 2.8 mm indicating that first increment formation occurs 3–4 days after hatching at 2.2 mm. Despite spatial and temporal differences in environmental factors, there were no significant differences in growth rates at any of three given sites over time, or between sites. Because larval presence only occurred at a narrow range of temperature (17–23.5 °C) and DO (6.5–9.3 mg·l^?1), in situ differences in growth did not appear to be because of differences in larval distribution and abundance patterns relative to these parameters.     

The behavior of Zn,Cd, Cu,Ni, Co,Fe, and Mn in anoxic baltic waters

In June 1981, dissolved Zn, Cd, Cu, Ni, Co, Fe, and Mn were determined from two detailed profiles in anoxic Baltic waters (with extra data for Fe and Mn from August 1979). Dramatic changes across the O₂H₂S interface occur in the abundances of Cu, Co, Fe, and Mn (by factors of ?100). The concentrations of Zn, Cd, and Ni at the redox front decrease by factors between 3 to 5.Equilibrium calculations are presented for varying concentrations of hydrogen sulfide and compared with the field data. The study strongly supports the assumption that the solubility of Zn, Cd, Cu, and Ni is greatly enhanced and controlled by the formation of bisulfide and(or) polysulfide complexes. Differences between predicted and measured concentrations of these elements are mainly evident at lower ΣH₂S concentrations.Cobalt proved to be very mobile in anoxic regions, and the results indicate that the concentrations are limited by CoS precipitation. The iron (Fe²⁺) and manganese (Mn²⁺) distribution in sulfide-containing waters is controlled by total flux from sediment-water interfaces rather than by equilibrium concentrations of their solid phases (FeS and MnCO₃). The concentrations of these metals are therefore expected to increase with prolonged stagnation periods in the basin.     

Arsenic,barium, germanium,tin, dimethylsulfide and nutrient biogeochemistry in Charlotte Harbor,Florida, a phosphorus-enriched estuary

Concentrations of dissolved nutrients (NO₃, PO₄, Si), germanium species, arsenic species, tin, barium, dimethylsulfide and related parameters were measured along the salinity gradient in Charlotte Harbor. Phosphate enrichment from the phosphate industry on the Peace River promotes a productive diatom bloom near the river mouth where NO₃ and Si are completely consumed. Inorganic germanium is completely depleted in this bloom by uptake into biogenic opal. The $\text{Ge}\text{Si}$ ratio taken up by diatoms is about 0·7 × 10^?6, the same as that provided by the river flux, confirming that siliceous organisms incorporate germanium as an accidental trace replacement for silica. Monomethylgermanium and dimethylgermanium concentrations are undetectable in the Peace River, and increase linearly with increasing salinity to the seawater end of the bay, suggesting that these organogermanium species behave conservatively in estuaries, and are neither produced nor consumed during estuarine biogenic opal formation or dissolution. Inorganic arsenic displays slight removal in the bloom. Monomethylarsenic is produced both in the bloom and in mid-estuary, while dimethylarsenic is conservative in the bloom but produced in mid-estuary. The total production of methylarsenicals within the bay approximately balances the removal of inorganic arsenic, suggesting that most biological arsenic uptake in the estuary is biomethylated and released to the water column. Dimethylsulfide increases with increasing salinity in the estuary and shows evidence of removal, probably both by degassing and by microbial consumption. An input of DMS is observed in the central estuary. The behavior of total dissolvable tin shows no biological activity in the bloom or in mid-estuary, but does display a low-salinity input signal that parallels dissolved organic material, perhaps suggesting an association between tin and DOM. Barium displays dramatic input behavior at mid-salinities, probably due to slow release from clays deposited in the harbor after catastrophic phosphate slime spills into the Peace River.     

Cadmium,cobalt, copper,iron, lead,nickel and zinc in Indian Ocean water

Results of trace-metal analyses of water samples obtained during a cruise with the Soviet R.V. “Akademik Kurchatov” in the Indian Ocean are presented. The determinations were performed on board with atomic absorption spectrophotometry after a two-stage dithiocarbamate—Freon extraction procedure. Trace-metal concentrations found are in the same range as those found recently for similar open-ocean areas by other workers. The values for lead and zinc are probably high due to contamination. Vertical profiles indicate biogenic processes as controlling factors for the increase of cadmium, copper and nickel concentrations with depth. Iron shows an irregular depth distribution as a result of large random variations in concentration.     

Northstar-Geology,Exploration History,and Development Status,Beaufort Sea,Alaska

Exploration for oil at Northstar has been long and costly. Northstar leases were first acquired in 1979 at a joint state and federal sale by Shell Oil, Amerada Hess, and Texas Eastern. The Northstar Unit is 6 mi offshore and about 4 mi northeast of the Point McIntyre Field. Oil was first discovered in Shell's Seal Island 1 in 1983. Five additional appraisal wells were drilled (1983-1986) from two man-made gravel islands in 40 ft of water. Early engineering estimates put the cost of development at $ 1.6 billion. In February 1995, BP Exploration (Alaska) acquired a 98 % interest in the Northstar Unit from Amerada Hess and Shell Oil. When developed by BP, Northstar will be the first oil produced from federal leases in Alaska. To date, the oil industry has invested in excess of $ 140 million in exploration and appraisal operations. An additional $ 90 million was spent on lease bonus bids. The giant Prudhoe Bay and Kuparuk Fields lie along the Barrow Arch. This arch is bounded to the north by a rift margin that deepens into the present-day offshore region. Northstar is located among a series of down-stepping faults off this northern rift margin of the Prudhoe Kuparuk high. The structure is a gently south-dipping northwest-trending faulted anticline. The crest of the structure is located near 10,850 ft subsea. The primary reservoir is the Ivishak Formation (325 ft thick) of the Sadlerochit Group. This is the same primary reservoir at Prudhoe Bay, approximately 12 mi to the south. At Northstar the Ivishak is a high-energy, coarse-grained conglomeratic facies of the Ivishak Formation. The primary lithology is a pebbly chert to quartz conglomerate with occasional sandstone. This very high net to gross reservoir appears to contain no regionally continuous permeability barriers. Cementation has reduced primary porosity to less than 15 %. Accurate porosity estimates are difficult to make due to the coarse-grained nature of the lithology and the presence of kaolinite and microporous chert. Permeability is highly variable, but averages 10 to 100 mDarcies. Oil is a very light and volatile 42 API crude with approximately 2,100 ft3 of gas per stock tank barrel of oil. This oil is very different from the heavier oils (26) found to the south in Prudhoe Bay. Estimated recoverable oil reserves range from 100 to 160 million barrels. A free-standing drilling rig is required at Northstar because the reserves are beyond extended-reach drilling techniques from shore-based facilities. The current development plan is to expand the existing Seal Island to about 5 acres. This is significantly less than Endicott's 40-acre island. The proposed drilling and produc tion island will be accessed by summer barges and winter ice roads. Oil, gas, and water will be processed at a stand-alone facility and then sent to shore via a subsurface pipeline. Northstar will have the first Arctic subsea pipeline in Alaska to transport oil to shore facilities (TAPS). Preliminary tests in Spring 1996 were very successful in demonstrating the technology to successfully bury a subsea pipeline safely in the Arctic.