抗差估计的初值选择

对L1 范估计的平差值和LS估计的平差值作为抗差估计的初值进行了比较 ,指出在 ρ函数是严凸函数时 ,二者无明显的区别。因为LS估计简单且易于计算 ,因此建议用LS估计的平差值作为抗差估计的初值。     

用遗传算法解算病态方程

对应用遗传算法解决病态方程问题进行了探讨。利用拟合法而不是通过法方程求解参数，从而避免了法方程系数求逆，使病态方程的解答有了较好的结果。通过模拟计算并和其他方法进行比较，证明该方法是可行的和有效的。     

The geochemistry of gem opals as evidence of their origin

Seventy-seven gem opals from ten countries were analyzed by inductively coupled plasma-mass spectrometry (ICP-MS) through a dilution process, in order to establish the nature of the impurities. The results are correlated to the mode of formation and physical properties and are instrumental in establishing the geographical origin of a gem opal. The geochemistry of an opal is shown to be dependant mostly on the host rock, at least for examples from Mexico and Brazil, even if modified by weathering processes. In order of decreasing concentration, the main impurities present are Al, Ca, Fe, K, Na, and Mg (more than 500 ppm). Other noticeable elements in lesser amounts are Ba, followed by Zr, Sr, Rb, U, and Pb. For the first time, geochemistry helps to discriminate some varieties of opals. The Ba content, as well as the chondrite-normalized REE pattern, are the keys to separating sedimentary opals (Ba > 110 ppm, Eu and Ce anomalies) from volcanic opals (Ba < 110 ppm, no Eu or Ce anomaly). The Ca content, and to a lesser extent that of Mg, Al, K and Nb, helps to distinguish gem opals from different volcanic environments. The limited range of concentrations for all elements in precious (play-of-color) compared to common opals, indicates that this variety must have very specific, or more restricted, conditions of formation. We tentatively interpreted the presence of impurities in terms of crystallochemistry, even if opal is a poorly crystallized or amorphous material. The main replacement is the substitution of Si⁴⁺ by Al³⁺ and Fe³⁺. The induced charge imbalance is compensated chiefly by Ca²⁺, Mg²⁺, Mn²⁺, Ba²⁺, K⁺, and Na⁺. In terms of origin of color, greater concentrations of iron induce darker colors (from yellow to “chocolate brown”). This element inhibits luminescence for concentrations above 1000 ppm, whereas already a low content in U (≤ 1 ppm) induces a green luminescence.     

Coupled redox transformations of catechol and cerium at the surface of a cerium(III) phosphate mineral

Highly insoluble Ce-bearing phosphate minerals form by weathering of apatite [Ca₅(PO₄)₃.(OH,F,Cl)], and are important phosphorous repositories in soils. Although these phases can be dissolved via biologically-mediated pathways, the dissolution mechanisms are poorly understood. In this paper we report spectroscopic evidence to support coupling of redox transformations of organic carbon and cerium during the reaction of rhabdophane (CePO₄·H₂O) and catechol, a ubiquitous biogenic compound, at pH 5. Results show that the oxic–anoxic conditions influence the mineral dissolution behavior. Under anoxic conditions, the release of P and Ce occurs stoichiometrically. In contrast, under oxic conditions, the mineral dissolution behavior is incongruent, with dissolving Ce³⁺ ions oxidizing to CeO₂. Reaction product analysis shows the formation of CO₂, polymeric C, and oxalate and malate. The presence of more complex forms of organic carbon was also confirmed. Near edge X-ray absorption fine structure spectroscopy measurements at Ce-M_4,5 and C-K absorption edges on reacted CePO₄·H₂O samples in the absence or presence of catechol and dissolved oxygen confirm that (1) the mineral surface converts to the oxide during this reaction, while full oxidation is limited to the near-surface region only; (2) the Ce valence remains unchanged when the reaction between CePO₄·H₂O and O₂ but in the absence of catechol. Carbon K-edge spectra acquired from rhabdophane reacted with catechol under oxic conditions show spectral features before and after reaction that are considerably different from catechol, indicating the formation of more complex organic molecules. Decreases in intensity of characteristic catechol peaks are accompanied by the appearance of new π^* resonances due to carbon in carboxyl (ca. 288.5 eV) and carbonyl (ca. 289.3 eV) groups, and the development of broad structure in the σ^* region characteristic of aliphatic carbon. Evolution of the C K-edge spectra is consistent with aromatic-ring cleavage and polymerization. These results further substantiate that the presence of catechol, O₂ (aq) causes both the oxidation of structural Ce³⁺ and the transformation of catechol to more complex organic molecules. Scanning Transmission X-Ray Microscopy measurements at the C K and Ce M_4,5 edges indicate three dominant organic species, varying in complexity and association with the inorganic phase. Untransformed catechol is loosely associated with CeO₂, whereas more complex organic molecules that exhibit lower aromaticity and stronger CO π^* resonances of carboxyl-C and carbonyl-C groups are only found in association with the grains. These results further serve as basis to postulate that, in the presence of O₂, CeO₂ can mediate the oxidative polymerization of catechol to form higher molecular weight polymers. The present work provides evidence for a pathway of biologically-induced, non-enzymatic oxidation of cerium and formation of small CeO₂ particles at room temperature. These findings may have implications for carbon cycling in natural and cerium-contaminated soils and aqueous environments.     

Evidence for crustal degassing of CF4 and SF6 in Mojave Desert groundwaters

Dissolved tetrafluoromethane (CF₄) and sulfur hexafluoride (SF₆) concentrations were measured in groundwater samples from the Eastern Morongo Basin (EMB) and Mojave River Basin (MRB) located in the southern Mojave Desert, California. Both CF₄ and SF₆ are supersaturated with respect to equilibrium with the preindustrial atmosphere at the recharge temperatures and elevations of the Mojave Desert. These observations provide the first in situ evidence for a flux of CF₄ from the lithosphere. A gradual basin-wide enhancement in dissolved CF₄ and SF₆ concentrations with groundwater age is consistent with release of these gases during weathering of the surrounding granitic alluvium. Dissolved CF₄ and SF₆ concentrations in these groundwaters also contain a deeper crustal component associated with a lithospheric flux entering the EMB and MRB through the underlying basement. The crustal flux of CF₄, but not of SF₆, is enhanced in the vicinity of local active fault systems due to release of crustal fluids during episodic fracture events driven by local tectonic activity. When fluxes of CF₄ and SF₆ into Mojave Desert groundwaters are extrapolated to the global scale they are consistent, within large uncertainties, with the fluxes required to sustain the preindustrial atmospheric abundances of CF₄ and SF₆.     

平鲷♀与真鲷♂的杂交研究

研究了不同盐度，温度，ｐＨ对平鲷Ｒｈａｂｄｏｓａｒｇｕｓ ｓａｒｂａ♀和真鲷Ｐａｇｒｏｓｏｍｕｓ ｍａｊｏｒ♂清子活力的影响，确立了人工授精与孵化的条件参数。平鲷♀与真鲷♂杂交的受精率达９５％以上，胚胎发育与其亲本的相似。经过超低温保存的真鲷精子的激活率，活力与鲜精的接近，其杂产的受精率也可达９５％以上。实验获得了杂产仔鱼，但杂交的孵化率比对照组低。     

南海大鹏湾夜光藻种群在其生态群落中的地位和功能

分析了１９９１年上半年南海大鹏湾盐田水域夜光菏和浮游动、植物之间的种群动态关系，结果表明，在春季高峰期３月至５月初，调查海域共出现１２个夜光藻和浮游动、植物高峰。其中，以发生４次赤潮的夜光藻种群占主导地位，其次是枝角类的鸟啄尖头蚤，其最高数量高达９６２３８ｉｎｄ／ｍ＾３。相比之下，在夜光藻和枝角类岛啄尖头捕食压力的影响下，浮游植物的春季高峰并不显著。调查结果表明夜光藻的过度繁殖，不但对产浮游性卵的     

珠江口东岸池养鲻鱼的年龄与生长

研究池养条件下鲻鱼ＭｕｇｉｌｃｅｐｈａｌｕｓＬｉｎｎａｅｕｓ的年龄和生长特性，结果表明，鳞片新年轮主要在１０—１月出现；鳞长与体长关系式为：Ｒ—０．００９０７Ｌ（０．７７６４）；Ｉ—Ｖ龄鱼体长和体重相对生长率和生长指标随着年龄增长而逐渐下降；体长与体重关系式为：Ｗ＝１．２７１６×１０（－５）Ｌ（３．０６９５），体长与全长关系式为：ＬＴ＝１０．３７１１＋１．１８０６ＬＢ，当年鱼体长和体重生长与月龄的关系分别为：ＬＢ＝８．６６６９＋２５．５７６９ｔ，Ｗ＝０．１１７０ｔ（３．５５３０），ｖｏｎＢｅｒｔａｌｌａｎｆｆｙ生长参数Ｌ∞＝６１３．２５ｍｍ，Ｋ＝０．３４１２，ｔ０＝－０．８２５，体重生长拐点值为２．４６ａ。     

海带的一个自然突变型

在多细胞藻的遗传学研究中,被发现的突变型很少[1].绿藻中有一些突变型,其中较多的是某种石莼(Ulva mutabilis)[2].三浦昭雄等在紫菜中发现突变型.在褐藻中未见有突变型的报道.这里所报道的是海带(Laminaria japonica)的一个突变型.