Acute toxicity of bromochlorinated seawater to selected estuarine species with a comparison to chlorinated seawater toxicity

The acute toxicity of bromochlorinated estuarine water (ca. 20%) was determined for several estuarine organisms. The most sensitive species were oysters (Crassostrea virginica, larvae and juveniles) and copepods (Acartia tonsa) with 48-h LC₅₀'s of 0·10 to 0·21 mg BrCl/litre. Palaemonetes pugio was most tolerant with a 96-h LC₅₀ of 0·70 mg BrCl/litre. The fish species tested (Menidia menidia, Brevoortia tyrannus and Leiostomus xanthurus) all had a 96-h LC₅₀ of 0·21–0·23 mg BrCl/litre.The BrCl toxicity data are compared with Cl₂ toxicity data for the same species. When the LC₅₀'s are expressed as equivalents per litre, BrCl is found to be two to four times less toxic than Cl₂. The ranking of species in terms of sensitivity is the same for both disinfectants.Some data are provided concerning the decay rates of BrCl and Cl₂ in estuarine water. BrCl was found to decay more rapidly than Cl₂ at higher ammonia levels (0·25 mg NH₄-N/litre). The question of chemical speciation is discussed with particular reference to the differential toxicities.     

Green's theorem and Green's functions for the steady-state cosmic-ray equation of transport

Green's Theorem is developed for the spherically-symmetric steady-state cosmic-ray equation of transport in interplanetary space. By means of it the momentum distribution functionF _o(r,p), (r=heliocentric distance,p=momentum) can be determined in a regionr _arr_bwhen a source is specified throughout the region and the momentum spectrum is specified on the boundaries atr _a andr _b . Evaluation requires a knowledge of the Green's function which corresponds to the solution for monoenergetic particles released at heliocentric radiusr _o , Examples of Green's functions are given for the caser _a =0,r _b = and derived for the cases of finiter _a andr _b . The diffusion coefficient is assumed of the form = _o(p)r ^b . The treatment systematizes the development of all analytic solutions for steady-state solar and galactic cosmic-ray propagation and previous solutions form a subset of the present solutions.     

油田开发中后期岩相单元的细分研究

油田开发中后期建立在原小层对比和沉积微相基础上的储层地质模型已不能适应调整挖潜和剩余油分布研究的要求,需要在小层划分的基础上,进一步细分到岩相单元。本文以大庆长垣南部葡北油田葡I组油层为例提出岩相单元的概念,通过现代沉积研究论证岩相单元细分的可行性,结合密井网测井曲线分析旋回性、隔夹层分布的稳定性及目前经济技术和采油工艺等,探讨细分单元的基本原则。最后提出岩相单元细分的基本方法。     

Terrestrial discharge influences microbioerosion and microbioeroder community structure in coral reefs

Microbioerosion rates and microbioeroder community structure were studied in four Kenyan protected coral-reef lagoons using shell fragments of Tridacna giant clams to determine their response to the influence of terrestrial run-off. Fourteen different microbioeroder traces from seven cyanobacteria, three green algae and four fungi species were identified. The river discharge-impacted reef and ‘pristine’ reef showed similar composition but higher microbioeroder abundance and total cyanobacteria- and chlorophyte-bioeroded areas when compared with the other study reefs. Cyanobacteria dominated during the north-east monsoon (NEM) relative to the south-east monsoon (SEM) season, with algae and cyanobacteria being major microbioeroders in the river-impacted and pristine reefs. The rate of microbioerosion varied between 4.3 g CaCO3 m^?2 y^?1 (SEM) and 134.7 g CaCO₃ m^?2 y^?1 (NEM), and was highest in the river-impacted reef (127.6 g CaCO₃ m^?2 y^?1), which was almost double that in the pristine reef (69.5 g CaCO₃ m^?2 y^?1) and the mangrove-fringed reef (56.2 g CaCO₃ m^?2 y^?1). The microbioerosion rates measured in this study may not be high enough to cause concern with regard to the health and net carbonate production of Kenya’s coral reefs. Nevertheless, predicted increases in the frequency and severity of stresses related to global climate change (e.g. increased sea surface temperature, acidification), as well as interactions with local disturbances and their influence on bioerosion, may be increasingly important in the future.     

Geochemical zoning around the McClean uranium deposits, Saskatchewan, Canada

Some 3400 drill core samples of the Athabasca Group and underlying regolith have been obtained by sampling 8-m sections from 55 diamond drill holes in the McClean Lake Area, Saskatchewan. Forty eight holes are from sections over six areas known to contain uranium mineralization and 7 are from unmineralized areas. The uranium zones are covered by 30 to 180 m of Athabasca sandstones and conglomerates.The uranium mineralization of the McClean deposits can be described as belonging to two different facies; a more reduced sulphide-arsenide facies and a more oxidized hematite-“bleached” facies, superimposed on any one of three host rocks.The sulphide-arsenide facies is probably older and, except in one deposit, it forms a patchy distribution of relicts. The principal pattern is an upwards increase in sulphur/arsenic ratio. The hematite-“bleached” facies appears to be younger and may represent a reworking of the earlier sulphide-arsenide facies mineralization under more oxidizing conditions.The trace metals can be grouped according to their redox behaviour. Vanadium, Mo and U, occurring as oxides, form one group while Ni, Co, Zn, Cu and As, occurring as sulphides and/or arsenides, form intermediate and most reduced groups, respectively. Iron is concentrated in the most oxidized facies as hematite or goethite and in the most reduced facies as pyritebravoite, siderite and chlorite. Manganese follows the distribution of siderite.The ratio of oxidized to reduced minerals can be represented by the ratio of U/Ni. This ratio can be used to estimate the variation of redox potential in the deposit at the time of deposition or alteration. The principal pattern is one of systematic increase in U/Ni ratio or oxidation potential both upward and to the northeast in each of the hematite and bleached facies.A generalized Eh-pH diagram is used to qualitatively describe the significance of each mineral facies.The U/Ni ratio of the transition between the hematite and “bleached” facies increases upwards. The phase diagram suggests that a possible cause is an upward decrease in pH and increase in Eh.The overall distribution is compatible with the origin of the deposits due to reduction at the interface between a plume of reductant emanating from fractures in the sub-Athabasca basement and an oxidizing aquifer moving southwestward in the sandstone. This model does not accurately predict the distribution of elements among the seven McClean Lake pods. However, it explains the overall pattern. Local variations in metal ratios in solution either in time or reflecting local provenance could be adduced to explain local deviations from the overall pattern.Clay alteration, apparently largely contemporaneous with the earliest mineralization, is largely illitic but with sporadic occurrences of xenotime and goyazite. Thus K and to some extent P, Y and light REE's are also enriched to some degree in the deposits.Uranium analysis of the drill core shows that there is little movement of U into the overlying sandstones from basement rocks and regolith that contain no uranium deposits. Uranium in the Athabasca sandstone from these areas averages less than 1 ppm. However, where uranium zones have been found in the basement rocks, regolith and lower Athabasca sandstone, U values greater than 2–3 ppm consistently occur in the overlying sandstones at or near surface.There appear to be two types of U anomalies, those that flank the deposits and those that directly overlie them. Both types exhibit vertical and lateral continuity. They are associated with vertical to steeply dipping fracture systems that traverse the Athabasca sandstone from basement to surface. The fractures are thought to be related to diagenetic processes from compaction of the sedimentary rocks over basement irregularities as well as tectonic processes (i.e. re-adjustment along old basement structures).These results suggest that target areas containing deeply buried uranium deposits could be defined by U analyses of the Athabasca sandstone from quite widely spaced holes of limited depth. This conclusion can be compared to XRD and chemical studies of clay mineral distribution within the Athabasca sandstone about the deposits.     

全球碳酸锂贸易格局与供应危机传播研究

随着新能源产业的快速发展, 全球碳酸锂贸易量逐渐增长, 但其出口集中于少数国家, 这意味着全球碳酸锂供应存在一定的风险。为了深入了解全球碳酸锂贸易格局演变、供应危机传播路径及影响, 本文构建了2000—2021年全球碳酸锂贸易网络和级联失效模型, 概述了主要出口国贸易流向和贸易格局演变过程, 并模拟了不同供应危机来源的雪崩规模、传播路径及其影响。我们得到: (1)20多年来全球碳酸锂贸易集中度逐渐增加, 出口前三位国家保持稳定, 而主要进口大国变化明显, 贸易格局已由南美供应全球转变为南美供应东亚; (2)碳酸锂贸易供应危机的影响范围逐渐扩大, 间接传播逐渐占据主导地位; (3)智利供应危机对中日韩的影响程度逐渐扩大, 但对欧洲的影响时间最长; 阿根廷和中国的雪崩规模在上升、传播次数增加, 而美国则相反。本文将贸易格局演变与危机传播结合, 明确了全球碳酸锂主要贸易国智利、阿根廷、中国、德国等作为供应危机来源的影响程度及其传播路径。以上分析结果将有利于维护全球碳酸锂贸易稳定和主要贸易国采取应对策略缓解供应危机。