Examination of Silicate Limitation of Primary Production in Jiaozhou Bay,China Ⅱ.Critical Value and Time of Silicate Limitation and Satisfaction of the Phytoplankton Growth

Analysis and comparison of Jiaozhou Bay data collected from May 1991 to February 1994 revealed the spatiotemporal variations of the ambient Si(OH)₄:NO₃ (Si:N) concentration rations and the seasonal variations of (Si:N) ratios in Jiaozhou Bay and showed that the Si:N ratios were <1 throughout Jiaozhou Bay in spring, autumn, and winter. These results provide further evidence that silicate limits the growth of phytoplankton (i.e. diatoms) in spring, autumn and winter. Moreover, comparison of the spatiotemporal variations of the Si:N ratio and primary production in Jiaozhou Bay suggested their close relationship. The spatiotemporal pattern of dissolved silicate matched well that of primary production in Jiaozhou Bay. Along with the environmental change of Jiaozhou Bay in the last thirty years, the N and P concentrations tended to rise, whereas Si concentration showed cyclic seasonal variations. With the variation of nutrient Si limiting the primary production in mind, the authors found that the range of values of primary production is divided into three parts: the basic value of Si limited primary production, the extent of Si limited primary production and the critical value of Si limited primary production, which can be calculated for Jiaozhou Bay by Equations (1), (2) and (3), showing that the time of the critical value of Si limitation of phytoplankton growth in Jiaozhou Bay is around November 3 to November 13 in autumn; and that the time of the critical value of Si satisfaction of phytoplankton growth in Jiaozhou Bay is around May 22 to June 7 in spring. Moreover, the calculated critical value of Si satisfactory for phytoplankton growth is 2.15–0.76 μmol/L and the critical value of Si limitation of phytoplankton growth is 1.42–0.36 μmol/L; so that the time period of Si limitation of phytoplankton growth is around November 13 to May 22 in the next year; the time period of Si satisfactory for phytoplankton growth is around June 7 to November 3. This result also explains why critical values of nutrient silicon affect phytoplankton growth in spring and autumn are different in different waters of Jiaozhou Bay and also indicates how the silicate concentration affects the phytoplankton assemblage structure. The dilution of silicate concentration by seawater exchange affects the growth of phytoplankton so that the primary production of phytoplankton declines outside Jiaozhou Bay earlier than inside Jiaozhou Bay by one and half months. This study showed that Jiaozhou Bay phytoplankton badly need silicon and respond very sensitively and rapidly to the variation of silicon. This study was funded by NSFC (No. 40036010) and subsidized by Special Funds from National Key Basic Research Program of P. R. China (G19990437), the Postdoctoral Foundation of Ocean University of Qingdao, the Director's Foundation of the Beihai Monitoring Center of the State Oceanic Administration and the Foundation of Shanghai Fisheries University.     

Sensitivity study of coastal plumes

INTRODUCTIONIn laboratory, Griffiths and Linden (1981 ) simulated the buoyancy-driven coastal currentsusing both a ring source and a point source in a rotating cylinder tank. The POint source was simifar to the river-forced plume in the coastal region. The coastal plume together with the gravitycoastal current moved along the coast, keeping the barrier on the right in the Northern Hemisphere. Stern et al. (1982) also conducted a similar experiment using a rectangular tank and carried ou…     

中国海带养殖现状与发展趋势

中国海带养殖规模与养殖产量均世界首位,并形成了一个集育苗、养殖、食品加工、藻类化工与生物制品开发于一体的链式产业,有关工作为我国海水养殖业的发展奠定了重要的理论、技术与实践基础.在国家高度重视资源与环境协调发展和渔业经济结构调整的深刻背景下,高新技术的研究与应用将是保障海带养殖产业优质、健康和高效发展的关键.     

黄河口沉积物重金属含量变化特征研究

在黄河口的平水期、枯水期和丰水期采集沉积物样品。分析了铜、铅、锌、镉、铬、砷、汞浓度.结果表明,黄河口沉积物样品中的重金属含量由河到海呈现先上升后下降的趋势,平水期和枯水期Cd、Cr、As呈显著相关(0.01水平)。重金属含量为平水期>枯水期>丰水期。水文特征严重影响到沉积物中重金属的迁移。沉积物中重金属含量和沉积物的粒度密切相关.粒度越小重金属含量越高,反映了河流沉积的特征。沉积物中重金属浓度较低。各项目基本上都符合海洋沉积物质量一类标准。     

Interannual variability in the sea surface cooling induced by tropical cyclones in the South China Sea

Sea surface cooling induced by tropical cyclones (TCs) is an important component of air-sea interactions. Using coordinate transformation and composite analysis...     

常德张家界高速公路慈利东互通段膨胀土工程特性及改性研究

在对常德张家界高速公路慈利东互通段工程地质综合测试、补充勘探的基础上 ,通过对膨胀土及其改良土进行了系统的试验研究 ,如自由膨胀率、有荷膨胀量、收缩、胀缩总率、颗粒分析、压缩、抗剪强度、承载比试验 ,评价了该段膨胀土的工程特性 ,对于指导膨胀土路基的设计与施工 ,具有重要的意义     

Fluid and melt inclusions in the Mesozoic Fangcheng basalt from North China Craton: implications for magma evolution and fluid/melt-peridotite reaction

Melt inclusions and fluid inclusions in the Fangcheng basalt were investigated to understand the magma evolution and fluid/melt-peridotite interaction. Primary silicate melt inclusions were trapped in clinopyroxene and orthopyroxene phenocrysts in the Fangcheng basalt. Three types of melt inclusions (silicate, carbonate, and sulfide) coexisting with fluid inclusions occur in clinopyroxene xenocrysts and clinopyroxene in clinopyroxenite xenoliths. In situ laser-ablation ICP-MS analyses of major and trace element compositions on individual melt inclusions suggest that the silicate melt inclusions in clinopyroxene and orthopyroxene phenocrysts were trapped from the same basaltic magma. The decoupling of major and trace elements in the melt inclusions indicates that the magma evolution was controlled by melt crystallization and contamination from entrapped ultramafic xenoliths. Trace element patterns of melt inclusions are similar to those of the average crust of North China Craton and Yangtze Craton, suggesting a considerable crustal contribution to the magma source. Calculated parental melt of the Fangcheng basalt has features of low MgO (5.96 wt%), high Al₂O₃ (16.81 wt%), Sr (1,670 ppm), Y (>35 ppm), and high Sr/Y (>40), implying that subducted crustal material was involved in the genesis of the Fangcheng basalt. The coexisting fluid and melt inclusions in clinopyroxene xenocrysts and in clinopyroxene of xenoliths record a rare melt-peridotite reaction, that is olivine + carbonatitic melt₁ (rich in Ca) = clinopyroxene + melt₂ ± CO₂. The produced melt₂ is enriched in LREE and CO₂ and may fertilize the mantle significantly, which we consider to be the cause for the rapid replacement of lithospheric mantle during the Mesozoic in the region.     

Rapid Determination of Trace Element Compositions in Peridotites by LA‐ICP‐MS Using an Albite Fusion Method

A rapid sample preparation procedure is described to determine trace element compositions of peridotites using LA‐ICP‐MS. Peridotite powders were fused with albite in a molybdenum–graphite assembly to obtain homogeneous glasses. Best conditions for the fusion procedure (heating at 1500–1550 °C for 10–15 min with a sample‐to‐flux ratio of 1:2) were constrained with melting experiments on two USGS reference materials, PCC‐1 and DTS‐2B. Mass fractions of first series transition elements, Ba and Pb, in quenched glasses of PCC‐1 and DTS‐2B are consistent with published data within 10% RSD. Three spinel peridotite xenoliths from eastern China were analysed following both our method and conventional solution ICP‐MS. Compared with solution ICP‐MS, the relative deviations of our method for most elements were within 10%, while for the REE, Ta, Pb, Th and U, the relative deviations were within 20%. In particular, volatile elements (e.g., Pb and Zn) are retained in the glass. Compared with conventional wet chemistry digestion, our method is faster. Additional advantages are complete sample fusion, especially useful for samples with acid‐resistant minerals (spinel and rutile), and long‐term conservation of glasses allowing unlimited repeated measurements with microbeam techniques. The same approach can be used for analyses of other mantle rocks, such as eclogites and pyroxenites.     

Zinc Isotopic Compositions of NIST SRM 683 and Whole‐Rock Reference Materials

In this study the homogeneity of the zinc isotopic composition in the NIST SRM 683 reference material was examined by measuring the Zn isotopic signature in microdrilled sample powders from two metal nuggets. Zinc was purified using AG MP‐1M resin and then measured by MC‐ICP‐MS. Instrumental mass bias was corrected using the “sample‐standard bracketing” method and empirical external normalisation with Cu doping. After evaluating the potential effects of varying acid mass fractions and different matrices, high‐precision Zn isotope data were obtained with an intermediate measurement precision better than ± 0.05‰ (δ⁶⁶Zn, 2s) over a period of 5 months. The δ⁶⁶Zn_JMC‐Lyon mean values of eighty‐four and fourteen drilled powders from two nuggets were 0.11 ± 0.02‰ and 0.12 ± 0.02‰, respectively, indicating that NIST SRM 683 is a good isotopic reference material with homogeneous Zn isotopes. The Zn isotopic compositions of seventeen rock reference materials were also determined, and their δ⁶⁶Zn values were in agreement with most previously published data within 2s. The δ⁶⁶Zn values of most of the rock reference materials analysed were in the range 0.22–0.36‰, except for GSP‐2 (1.07 ± 0.06‰, n = 12), NOD‐A‐1 (0.96 ± 0.03‰, n = 6) and NOD‐P‐1 (0.78 ± 0.03‰, n = 6). These comprehensive data should serve as reference values for quality assurance and interlaboratory calibration exercises.