南海北部海区水团的判别分析

将判别分析应用于南海北部海区的水团分析。划分为八个水团:沿岸冲淡水团(F),近岸混合水团(M),暖表层水团(WS),表层水团(S),表—次层混合水团(SU),次层水团(U),次—中层混合水团(UI)和中层水团(I)。给出了各水团在四季代表月的Bayes多组判别的系数和参数。用资料检验判别的成效.冬季和春季可达95.90％以上,夏季为94.80％,秋季是全年最低值,为92.72％。讨论了造成错判的原因,并与Fisher判别作了比较。当测值维数较低时,建议选用Bayes判别。对八个水团以及各水团两两之间差异的显著性进行了检验,证实在每个季节中各水团之间的差异,都在高度置信水平(α=0.01)上具有显著性。因而,划分为八个水团是有实际意义的,其判别式的系数和参数,可用于实际的判别和预报。     

Coral Recruitment and Regeneration on a Maldivian Reef 21 Months after the Coral Bleaching Event of 1998

Abstract. This paper describes the quantitative inventory of stony corals on a Maldivian reef after the bleaching event of 1998. The detailed data, collected in March 1999 and March 2000, comprise survival, new recruitment and regenerates. They were obtained in 6 transects laid out randomly on the reef flat, on 22 Acropora tables on 6 sites at the reef edge and on 39 Porites lobata blocks and 1 Diploastrea heliopora colony. The present cover of living zooxanthellate corals is reduced to ca. 2 – 5 % of its previous state. Acroporidae and Pocilloporidae were practically wiped out, while Poritidae survived partly and Agariciidae (esp. Pavona) are now the dominant group. New settlements on dead Acropora tables were mainly Agariciidae, followed by Acroporidae and Pocilloporidae. Regenerates on Porites were pronounced and the apparent yearly increase in mass was about threefold that of Diploastrea, which is 3 – 4 mm per year. The influence on reef ecology in terms of coral substrate and species, possible sources of larvae, change of guilds in reef builders, other species and the prospect for further development of the reef, with respect to growth versus erosion, is discussed.     

Calculation of the added mass of circular cylinders in shallow water

The added mass of hull section shapes must be known, in order to carry out any studies of ship motions, which may be associated with either seakeeping or manoeuvring. Determination of the added mass in deep water can involve conformal mapping or surface singularity distributions. However, in shallow water the problem of determining the added mass is made more difficult by the proximity of the seabed. In this paper, three approaches to the problem of finding the added mass of semi-circular sections are explored. Although there is no known exact solution to this problem, the relationships given by the three methods are compared and the approximate nature of the solutions is examined. The first method is a series solution, which is taken here to include more terms than are normally given in the existing literature. The other two solutions are considered to be new, and so are given in some mathematical detail.     

饱和流体多孔介质中AVA特征分析及储层参数反演研究

AVA(Amplitude Versus Angle)技术是基于常规介质模型(均匀各向同性介质模型)发展起来的,由于忽略了储层的孔隙结构和充填流体的影响,造成AVA特征中是部分对地震波能量的吸收和衰减作用反映不足.从振幅特征方程的实际应用出发,建立起各参数与常规岩性参数之间的关系.以Gassmann方程与Biot理论为基础,推导出振幅特征方程中弹性参数与常规岩性、储层参数(如:纵波速度、横波速度、密度、孔隙度、流体参数Kf)之间的转化关系式,详细研究饱和流体多孔介质模型中的AVA特征,比较该介质模型与常规介质模型在AVA特征上的差异,并将饱和流体多孔介质AVA技术应用于川西凹陷深层须家河组储层预测,通过多波AVA储层参数的反演研究,为直接利用地震资料进行储层识别并进一步识别其流体特征提供了一种有力手段.     

兰州—白银多目标地球化学调查野外工作方法浅析

多目标区域地球化学调查从调查区表层、深层采样土壤元素分布特征入手建立土壤元素地球化学分配机制,以景观、地貌及地质特征为基础,选择合理的采样位置,正确的采样方法、采样层位,应用掌上机（Pocket PC）及数字填图系统（Rgmap）采集野外样品,本文以兰州—白银黄土覆盖区景观区为例,对表层、深层采样方法和技术要求进行探讨,对全省开展多目标地球化学调查,特别是野外工作方法提供借鉴。     

淮南刘庄煤矿地基人工冻融土工程性质与中微观结构之间关系研究

以淮南刘庄煤矿主井地基的人工冻融土为研究对象,以偏光显微镜,扫描电镜（SEM）为主要研究手段,研究分析了人工冻融土与原状土的中微观结构、冻融前后的中微观结构的变化规律及内在原因。此外,还研究分析了人工冻融土冻融前后的中微观结构及其变化与人工冻融土的物理、力学、工程性质之间的关系。研究显示中微观结构对人工冻融土的物理、力学、工程性质有很大的影响,冻融前后中微观结构的变化受到土的种类、埋深、原状土的中微观结构等因素的影响,且冻融前后的中微观结构的变化在一定程度上主导了冻融前后的物理、力学、工程性质的改变。     

节理岩体卸荷强度特性的试验研究

卸荷状态工程岩体的强度特性与传统的加载岩体有本质的区别。目前对于岩石卸荷强度特性的研究比较多见,但对于含节理的岩体在卸荷应力状态下的强度特性,尤其是节理面对其强度的影响研究实属少见。本文通过岩体三轴模拟试验研究了卸荷应力状态下节理岩体的破坏特征,突出考虑了节理面性质对卸荷强度的影响,在此基础上提出了节理岩体卸荷强度准则的一般表达式并进行了对比验证。     

Zircon M257 ‐ a Homogeneous Natural Reference Material for the Ion Microprobe U‐Pb Analysis of Zircon

We introduce and propose zircon M257 as a future reference material for the determination of zircon U‐Pb ages by means of secondary ion mass spectrometry. This light brownish, flawless, cut gemstone specimen from Sri Lanka weighed 5.14 g (25.7 carats). Zircon M257 has TIMS‐determined, mean isotopic ratios (2s uncertainties) of 0.09100 ± 0.00003 for ²⁰⁶pb/²³⁸U and 0.7392 ± 0.0003 for ²⁰⁷pb/²³⁵U. Its ²⁰⁶pb/²³⁸U age is 561.3 ± 0.3 Ma (unweighted mean, uncertainty quoted at the 95% confidence level); the U‐Pb system is concordant within uncertainty of decay constants. Zircon M257 contains ～ 840 μg g^?1 U (Th/U ～ 0.27). The material exhibits remarkably low heterogeneity, with a virtual absence of any internal textures even in cathodoluminescence images. The uniform, moderate degree of radiation damage (estimated from the expansion of unit‐cell parameters, broadening of Raman spectral parameters and density) corresponds well, within the “Sri Lankan trends”, with actinide concentrations, U‐Pb age, and the calculated alpha fluence of 1.66 × 10¹⁸ g^?1. This, and a (U+Th)/He age of 419 ± 9 Ma (2s), enables us to exclude any unusual thermal history or heat treatment, which could potentially have affected the retention of radiogenic Pb. The oxygen isotope ratio of this zircon is 13.9%o VSMOW suggesting a metamorphic genesis in a marble or calc‐silicate skarn.     

Composition-Induced Variations in SIMS Instrumental Mass Fractionation during Boron Isotope Ratio Measurements of Silicate Glasses

An analytical artefact is reported here related to differences in instrumental mass fractionation between NIST SRM glasses and natural geological glasses during SIMS boron isotope determinations. The data presented demonstrated an average 3.4‰ difference between the NIST glasses and natural basaltic to rhyolitic glasses mainly in terms of their sputtering-induced fractionation of boron isotopes. As no matrix effect was found among basaltic to rhyolitic glasses, instrumental mass fractionation of most natural glass samples can be corrected by using appropriate glass reference materials. In order to confirm the existence of the compositionally induced variations in boron SIMS instrumental mass bias, the observed offset in SIMS instrumental mass bias has been independently reproduced in two laboratories and the phenomenon has been found to be stable over a period of more than one year. This study highlights the need for a close match between the chemical composition of the reference material and the samples being investigated.     

Recommended Values of 239Pu, 240Pu and 239+240Pu Concentrations in Reference Material IAEA-315 (Marine Sediment) Estimated by Thermal Ionisation Mass Spectrometry, Inductively Coupled Plasma-Mass Spectrometry and Alpha Spectrometry

The recommended concentrations of ²³⁹Pu, ²⁴⁰Pu and ^239+240Pu in reference material IAEA‐315 (marine sediment) were estimated by three analytical methods: isotope dilution thermal ionisation mass spectrometry (TIMS), isotope dilution inductively coupled plasma‐mass spectrometry (ICP‐MS) and alpha spectrometry. The determination of ²³⁹Pu and ²⁴⁰Pu (^239+240Pu by alpha spectrometry) was carried out with samples from randomly selected bottles using each method. Plutonium‐238 was also measured by alpha spectrometry. A plutonium‐242 reference material was used as a spike for the quantitative analysis. The influence of ²⁴²Pu in the samples was therefore calculated; however, this contribution was less than the range of uncertainty and did not influence the final results. The obtained data were statistically analysed using variance component analysis and paired comparison. The combined standard uncertainties from “method/measurement”, “bottle” and “sub‐sample” were in the order of 3 to 6%. The main contributions to the uncertainty were from the material heterogeneity and from systematic differences between methods. Based on this study with twenty‐seven analyses using 10–14 g sample mass, concentrations of (38 ± 3) Bq kg^?1, (28 ± 3) Bq kg^?1 and (66 ± 4) Bq kg^?1 are proposed as recommended values for ²³⁹Pu, ²⁴⁰Pu and ^239+240Pu, respectively, and (9.5 ± 0.4) Bq kg^?1 for ²³⁸Pu as an information value in reference material IAEA‐315. In mass concentration units, these amount to (16.4 ± 1.2) ng kg^?1, (3.3 ± 0.4) ng kg^?1 and (0.015 ± 0.003) ng kg^?1 for ²³⁹Pu, ²⁴⁰Pu and ²³⁸Pu, respectively. The certified reference materials NIST 4350B and NIST 4354 were also analysed by TIMS for quality assurance of the method used in this study.