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Abstract. Benthic fluxes of dissolved N. Si and P nutrients, alkalinity, dissolved inorganic C (DIC), and O2 from sediments in the Gulf of Trieste (northern Adriatic, Italy) were measured monthly for 16 months, using laboratory incubated flux chambers at in siru temperatures in the dark. The annual average fluxes were: 02 = -19.3 ± 8.2, DIC = 13.7 ± 9.6, NO3 = -0.04 ± 0.16, NH4 = 0.3 ± 0.4. PO4= 4.001 ± 0.01, Si = 0.9 ± 0.1 mmol m-2 d-1, with strong temporal fluctuations. The highest effluxes of all nutrients and DIC were observed in the summer. Small effluxes of DIC and NH4 and influxes of Si and PO4 were observed in late winter. Only NH4 (ca. 50%) and Si (ca. 70%) fluxes were significantly correlated with temperature. This correlation suggests that the rate of downward input and the quality of sedimented organic matter (autochthonous and allochthonous) were superimposed on the temperature fluctuations. High DIC, NH4 and Si effluxes observed in May 1993 during low temperature were due to the degradation of sedimentary organic matter produced by an early spring bloom of benthic microalgae which occurred about 6 weeks earlies while the autumn phytoplankton bloom was simultaneously reflected in enhanced benthic fluxes due to higher temperature. The role of benthic biological advection in this transport across the sediment-water interface, evaluated by comparison between measured benthic and calculated diffusive fluxes from nutrient pore water concentrations, was of minor importance. This is probably due to low infaunal activity throughout the year it was localized mostly in the narrow surficial layer. The annual average diffusive fluxes of NH4 and PO4 were higher than those measured, probably due to the presence of nitrificationdenitrifi-cation processes and redox-dependent chemical reactions at the oxic sediment-water interface, respectively. Only during bottom-water hypoxia in September 1993 did strong PO4 effluxes prevail. Calculations based on the Redfield stoichiometry of oxic decomposition of organic N to NH4 and NO3, and differences between diffusive and measured NH4 fluxes showed that denitrifkation averaged 0.8 mmol m-2 d-1. Significant correlations between NH4 and PO4 DIC and Si, and NH4 and Si fluxes suggested their parallel regeneration and utilization at the sediment-water interface. The nutrient fluxes observed were not significantly linked to O2 consumption, suggesting also that anaerobic oxidation processes were important at the sediment-water interface in the gulf. The N, P and Si nutriqnts released from sediment pore waters are probably utilized in benthic microalgal and bottorn-hater primary production. This indicates that pelagic and benthic communities in the central part of the Gulf of Trieste function relatively independently of each other.  相似文献   
13.
Abstract. The importance of sponge spicules in the turnover of biogenic silica (BSi) in the detritic bottoms of the Eastern Ligurian Riviera was evaluated by studying sediment cores and the detrital matter collected by a trap over a one year period.
This study made evident that: i) Sponge spicules represent the main component of the BSi both in the sediments and in the trapped matter; ii) A correlation exists between the sponge biomass present on the overhanging cliff and the amount of sponge spicules found in the sediment below; iii) Inside the sediments, a superficial layer (10 cm deep) characterized by intensive silica dissolution processes can be observed; and iv) The amount of spicules collected using the trap is not constant throughout the year, but shows a characteristic trend with low values in spring and summer and high values in autumn and winter.  相似文献   
14.
采用2. 0 mol/dm~3Na_2CO_3溶液5h单点化学提取-硅钼蓝连续分光光度分析法分别测定了大亚湾西部海域13个表层沉积物和1个沉积物岩芯中生物硅的含量.表层沉积物和沉积物岩芯中生物硅含量占比分别为0. 69%~2. 02%和1. 24%~2. 05%,平均值分别为1. 42%和1. 60%.结果证实西大亚湾沉积物中生物硅含量水平与我国南海近岸海域基本一致.在210Pbex测年的基础上,通过分析沉积物岩芯中生物硅、有机物、无机碳等多指标,揭示近百年来大亚湾周边环境变化对海洋环境的影响,证实了上世纪80年代以来西大亚湾周边农业、海水养殖业和工业发展等人类活动加剧了该海域生态环境变化,尤其90年代核电站运行对海洋生态变化造成一定的影响.  相似文献   
15.
以烟台四十里湾作为研究区域,分析了16个站位表层沉积物中生物硅的含量,探讨沉积物中生物硅对内湾环境的指示作用.结果表明,污水排放区、垃圾倾倒区沉积物中生物硅含量较高(平均值分别为0.71%和0.78%),对应上层水体的富营养化;航道区生物硅含量很低(平均值0.37%),与航船扰动造成的低生产力状况符合.沉积物中生物硅含量较好地反映了上层水体的浮游植物状况,并与上层营养盐浓度具有很好的对应关系.研究表明,沉积环境能够明显影响沉积物中生物硅的沉积和保存.  相似文献   
16.
以2011年6月和8月在长江口邻近海域采集的沉积物和间隙水样品为研究对象,讨论了沉积物中生物硅(BSi)和间隙水中溶解硅(DSi)的分布情况和影响因素,并初步探讨了生物硅的循环和保存。结果表明,表层沉积物中BSi的含量较低,且均小于1%。柱状沉积物中BSi的含量范围为0.34%~0.52%。C3、D1站位柱状沉积物中BSi的记录主要是由早期成岩过程控制,33#站位的分布特征主要是由水动力等变化控制。沉积物间隙水中DSi的浓度范围为101.6~263.9 μmol/L,低于纯BSi的溶解度;间隙水的pH值越大,沉积物的含水率越低,还原性越强,间隙水中DSi的含量越高。3站位生物硅的埋藏效率均较高,表明长江口邻近海域是潜在的硅的汇。沉积通量的分布与沉积速率和埋藏效率的分布一致,均有近岸高于远海的趋势。  相似文献   
17.
Problems with biogenic silica measurement in marginal seas   总被引:5,自引:0,他引:5  
Surface sediment samples from the Bohai, Yellow Sea, and the Pacific were used to assess biogenic silica (BSi) content and to study uncertainties in BSi measurements. The contents of BSi in the Bohai and Yellow Sea are all less than 1%. The dissolution of BSi in sediments from the Bohai and Yellow Sea is very important to maintain high levels of silicate in the water column. The non-biogenic silica from clay minerals has an obvious effect on BSi of sediment samples in the Bohai and Yellow Sea with low BSi and high clay minerals. The solid to solution ratio was found to have a great influence on BSi measurement, which can induce uncertainties up to 75%. The effect of loss by sorption and centrifugation is negligible. Interlaboratory comparison of techniques for BSi measurement by the wet alkaline extraction technique of Mortlock and Froelich [Deep-Sea Res. 36 (1989) 1415-1426] with clay correction was suggested to give no significant differences. However, differences in sediment compositions and reagent to sample ratio may limit the application of the wet alkaline extraction method.  相似文献   
18.
春季长江口及邻近海域悬浮颗粒态硅的研究   总被引:2,自引:0,他引:2       下载免费PDF全文
对春季长江口及邻近海域悬浮颗粒态生物硅(PBSi)、成岩硅(LSj)进行了大面调查和围隔培养实验研究,讨论了悬浮颗粒物中PBSi的分布情况及其影响因素.分析表明,PBSi与LSi的含量分别为0.22~4.25和1.75~184μmol/dm<'3>,与世界其他海域相比LSi的含量偏高,PBSi含量则处于中等水平.由于陆...  相似文献   
19.
Vertical and seasonal characteristics of biogenic silica (BSi) dissolution in seawater were investigated by multiple dissolution experiments using seawater collected from surface and mesopelagic layers in Suruga Bay during the period 2002–2004. The dissolution rate coefficients calculated based on temporal changes of BSi concentration varied with the season of sample collection. They ranged from 0.023–0.057 day− 1 for surface samples and 0.0018–0.0025 day− 1 for mesopelagic samples for temperatures approaching in situ conditions. Experiments at various temperatures confirmed that BSi dissolution depends on temperature in natural seawater. Dissolution rate coefficient (day− 1) of BSi correlated significantly with temperature (°C), and Q10 was 2.6. Addition of bioavailable organic matter to low-bioactivity seawater enhanced the protease activity and abundance of bacteria, and increased BSi dissolution rate by a factor of 1.4–2.0. There is clear evidence that BSi dissolution is accelerated by bacterial activity and potentially limited by bioavailable organic matter in natural seawater. Dissolution rates and total decreases of BSi concentration were lower during experiments using mesopelagic samples than in those using surface samples. This suggests that dissolution of BSi varies with depth and that BSi in the mesopelagic water is more resistant to the dissolution than that in the surface water. This lower dissolution rate was caused by lower temperature and lower bacterial activity due to less bioavailable organic matter in mesopelagic water. Our results provide a mechanistic understanding of variations in silica cycling within the seasonally and vertically differing marine environment.  相似文献   
20.
Moored sediment traps were deployed from January 2004 through December 2007 at depths of 550 and 800 m in San Pedro Basin (SPB), CA (33°33.0′N, 118°26.5′W). Additionally, floating sediment traps were deployed at 100 and 200 m for periods of 12-24 h during spring 2005, fall 2007, and spring 2008. Average annual fluxes of mass, particulate organic carbon (POC), ??13Corg, particulate organic nitrogen (PON), ??15N-PON, biogenic silica (bSiO2), calcium carbonate (CaCO3), and detrital material (non-biogenic) were coupled with climate records and used to examine sedimentation patterns, vertical flux variability, and organic matter sources to this coastal region. Annual average flux values were determined by binning data by month and averaging the monthly averages. The average annual fluxes to 550 m were 516±42 mg/m2 d for mass (sdom of the monthly averages, n=117), 3.18±0.26 mmol C/m2 d for POC (n=111), 0.70±0.05 mmol/m2 d for CaCO3 (n=110), 1.31±0.21 mmol/m2 d for bSiO2 (n=115), and 0.35±0.03 mmol/m2 d for PON (n=111). Fluxes to 800 and to 550 m were similar, within 10%. Annual average values of ??13Corg at 550 m were −21.8±0.2‰ (n=108), and ??15N averages were 8.9±0.2‰ (n=95). The timing of both high and low flux particle collection was synchronous between the two traps. Given the frequency of trap cup rotation (4-11 days), this argues for particle settling rates ≥83 m/d for both high and low flux periods. The moored traps were deployed over one of the wettest (2004-2005, 74.6 cm rainfall) and driest (2006-2007, 6.6 cm) rain years on record. There was poor correlation (Pearson's correlation coefficient, 95% confidence interval) of detrital mass flux with: Corg/N ratio (r=0.10, p=0.16); ??15N (r=−0.19, p=0.02); and rainfall (r=0.5, p=0.43), suggesting that runoff does not immediately cause increases in particle fluxes 15 km offshore. ??13Corg values suggest that most POC falling to the basin floor is marine derived. Coherence between satellite-derived chlorophyll a records from the trap location (±9 km2 resolution) and SST data indicates that productivity and export occurs within a few days of upwelling and both of these parameters are reasonable predictors of POC export, with a time lag of a few days to 2 weeks (with no time lag—SeaWiFS chlorophyll a and POC flux, r=0.25, p=0.0014; chlorophyll a and bSiO2 flux, r=0.28, p=0.0002).  相似文献   
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