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111.
Spatio-temporal changes in totally and enzymatically hydrolyzable amino acids (THAA and EHHA) and EHAA/THAA ratios of superficial sediments were assessed during 1997-1999 in three areas (i.e., the Gulf of Lions, the Bay of Biscay, and Central Chile) differing in their primary productivity. In all three areas, and even off Central Chile where a strong El Niño event took place during 1997-1998, spatial changes were always much greater than temporal ones. The factors affecting the spatial distributions of amino acid concentrations differed among areas. In the Gulf of Lions, sediment granulometry was apparently the most important driving force of THAA, EHAA, and EHAA/THAA, and there was no marked difference between stations located on the open slope and those in submarine canyons. Conversely, in the Bay of Biscay, there were clear differences between the stations located off Cap-Breton, on the open slope, and those in the Cap-Ferret canyon; the latter two featuring lower EHAA and THAA but higher EHAA/THAA. This pattern is likely to result from the predominance of different sources of organic matter and especially from the importance of continental inputs to the Cap-Breton canyon. Off Central Chile, amino acid concentrations and ratios were both maximal around 100 m depth, probably reflecting the interaction between the primary productivity gradient and the presence of an oxygen minimum zone (OMZ) reducing the degradation of sedimentary organics. When comparing the average values collected in the three areas studied, THAA and EHAA were highest in Central Chile, intermediate in the Bay of Biscay and lowest in the Gulf of Lions. EHAA/THAA ratios were also highest in Central Chile but were lowest in the Bay of Biscay. Differences between the Gulf of Lions and the Bay of Biscay could have been affected by sampling design. In Central Chile, the use of labile organic carbon to total organic carbon (C-LOM/TOC) and EHAA/THAA as indices of organic matter lability led to very similar results. This was not the case in the Bay of Biscay. It is therefore argued that the use of C-LOM/TOC should be restricted to highly productive areas.  相似文献   
112.
盐度对隐杆藻类胡萝卜素及脂肪酸含量的影响   总被引:2,自引:0,他引:2  
于1992年6月,采集分离江苏台南盐场盐生隐杆藻,通过不同浓度的NaCl研究盐度对类胡萝卜素、脂肪酸含量的影响;类胡萝卜素,依Jones等(1974)方法提取,脂肪酸依Schwarzenbach等(1978)方法提取。结果表明,在0.5—1.5mol/LNaCl培养基中,类胡萝卜素的百分含量从2.76%下降到0.67%;然而当培养基NaCl浓度增加到3.5mol/L时,类胡萝卜素的百分含量又开始上升,到2.31%。在低盐度(NaCl,0.5-1.0mol/L)和高盐度NaCl,3.0-3.5mol/U)下培养的盐生隐杆藻中,总脂肪酸的含量高于中盐度(NaCl,10-25mol/L)的;软脂肪酸含量变化同总脂肪酸相似;此外,在不同盐度下各种脂肪酸的相对百分含量也是变化的。  相似文献   
113.
Advances in analytical techniques now allow for the potential analysis of intact peptides and proteins isolated from marine sediments. However, there is no established technique for the extraction of macromolecular materials from marine sediments. Six different methods for extracting the amino acid component from coastal marine sediments were compared to the standard hot acid hydrolysis technique for their percent recovery and amino acid composition. The standard hot acid hydrolysis on dried, whole sediments released the greatest concentration of total amino acids (PS-THAA; 3.52 mg gdwt 1 ± 10% (SMD)), yet this only accounted for 22% of the total nitrogen in Puget Sound sediments (Washington, USA). Repeated hydrolysis of the same samples did not improve the recovery of nitrogen by more than an additional 10%. Base extraction (0.5 N NaOH) was the second best method for recovering amino acid nitrogen, releasing 60% of the Puget Sound total hydrolyzable amino acids (PS-THAA) (corresponding to 13% of the total sedimentary nitrogen), and has the advantage that it does not rely on peptide hydrolysis to free the nitrogenous component from the sediment matrix. The amino acid distribution of the 0.5 N NaOH extract was not significantly different than the initial THAA. Other non-hydrolyzing methods released lower yields of amino acids (Triton X-100 ≥ hot water > 50 mM NH4HCO3 > HF), but might prove to be of use to investigators interested in specific fractions of sedimentary organic nitrogen because these four methods had distinctly different amino acid compositions (enrichments in basic amino acids and depletions in acidic amino acids). Treatments with HF both before and after traditional hydrolysis and/or extractions with base did not release any more of the sedimentary nitrogen. Our results are consistent with the hypothesis that a large fraction of the sedimentary nitrogen (TN) is protected within an organic matrix.  相似文献   
114.
Total suspended matter was collected along the Yangtze River (Changjiang) and in the East China Sea in April to May and in September 2003, respectively, to study origin and fate of particulate organic nitrogen. Concentrations of particulate organic carbon (POC), nitrogen (PN) and hydrolyzable particulate amino acids (PAA; d- and l-enantiomers) were higher in the Yangtze Estuary than in the river and decreased offshore towards the shelf edge. In the coastal area, higher values of PAA were observed in the surface layer than in the bottom water. Stable carbon isotope ratios (δ13C) of POC increased from − 24.4‰ in the river to values around − 21‰ on the East China Sea Shelf. Dominant amino acids were aspartic acid + aspartine (Asx), glutamic acid + glutamine (Glx), glycine, alanine and serine. The proportions of Asx, Glx and isoleucine were higher in the marine than in the riverine samples contrary to the distributions of glycine, alanine, threonine and arginine. The proportions of d-amino acids were highest in the riverine suspended organic matter (6% of PAA) decreasing towards the shelf edge (1.5% of PAA). d-arginine, not reported in natural aquatic samples so far, was the most abundant d-amino acid in the river. The amino acid composition of the particulate organic matter (POM) in the Yangtze River indicates an advanced stage of degradation of POM. Highly degraded organic matter from soils is probably a main source of POM in the Yangtze River, but the relatively high δ13C values and low C/N ratios (7.7 ± 1.6) also indicate contribution from anthropogenic sources. The degraded riverine material was a dominant organic matter source in the estuary, where aquatic primary production had only a small overall contribution. In the East China Sea, gradual settling of riverine organic matter and the addition of fresher phytoplankton impacted the amino acid composition and δ13C values, and on the outer shelf relatively fresh phytoplankton-derived organic matter dominated.  相似文献   
115.
Characterization of the proteinaceous matter in marine aerosols   总被引:1,自引:0,他引:1  
Marine aerosols play a dominant role in the transfer of oceanic material to the atmosphere. Most marine aerosol originates when air bubbles burst at the sea surface ejecting material from the sea surface microlayer and bubble surface layers into the air. Concentrations of chemical compounds in these surface layers often differ from their concentrations in bulk water. We examined the enrichment of aerosols with proteinaceous matter and attempted to characterize the physical nature and sources of this matter. We measured concentrations of dissolved free (DFAA), dissolved combined (DCAA), and particulate (PAA) amino acids, transparent stainable particles (TSP), and bacteria and virus-like particles as carriers of protein, in natural and simulated aerosols. We also evaluated D/L ratios certain amino acids in all amino acid fractions.DFAA and DCAA enriched the aerosols we sampled by 1.2–20 times compared to bulk seawater; PAA enrichment was usually higher (up to 50-fold). Aerosols contained particles typical of seawater, e.g., microorganisms, organic debris, inorganic particles with adsorbed organic matter, but also a large number of semitransparent gel-like particles, which all contained amino acids. Some of these particles were probably scavenged from bulk water, but new particles produced as bubbles burst at the surface comprised at least 10% of total proteinaceous matter in the aerosol. D/L ratios of certain amino acid suggested that the particles were most likely made from dissolved polymers secreted by phytoplankton that were concentrated on bubble surfaces and in the microlayer. Examination with Alcian Blue (a dye that targets carbohydrates) and Coomassie Blue (a dye that targets proteins) showed that most TSP in the aerosols contained both proteins and polysaccharides. Microorganisms enriched the aerosols by up to two orders of magnitude, but contributed less than 4% to the total protein pool.  相似文献   
116.
大亚湾海域溶解游离氨基酸及其与环境的关系   总被引:4,自引:0,他引:4  
对大亚湾海域溶解游离氨基酸(DFAA)的分布特征及其影响因素进行了研究。现场采样调查分别于1995年5月、11月和2000年4月进行。结果表明 :(1)大亚湾海域DFAA的含量较高 ,在0.69~4.73μmol/L之间 ,平均2.16±0.87μmol/L,可能主要源于较为旺盛的生物活动 ;(2)DFAA含量在海域的平面分布变化较大 ,垂直分布和季节及年变化不明显 ;(3)DFAA与海水中的DOC呈正相关、与叶绿素呈负相关关系 ,与TIN的相关性则呈季节变化 ,生物效应可能是影响该海域DFAA含量的主要因素。  相似文献   
117.
Particulate samples were collected from the Changjiang river system during a flood period, in May 1997, and POC, stable isotope and lipids associated with particles were examined. Results showed the decrease (0.84% ~ 1.88%) of organic carbon content from the upper reaches to the estuary.δ13C values of particulate organic carbon was in the range of -24.9×10-3 to -26.6×10-3, which were close to the isotopic signature of continental C3 vegetation. Total particulate n-alkanes concentrations varied from 1.4 to 10.1μg/dm3,or from 23.7 to 107μg/g of total suspended matter. Fatty acids were present in all the samples, from 1.4 to 5.4μg/dm3, with saturated and unsaturated straight-chain and branched compounds in the carbon number range from C12 to C30. Both δ13C and the ratio of carbon content to nitrogen content indicate the predominance of terrestrial inputs (soil organic matter) among the particles. The biomarker approach has been used to identify the relative portion of terrigenous and autochthonous fraction in the particulate samples. The distribution of fatty acids suggests a striking phytoplanktonic and microbial signal in most particle samples. The terrestrial alkanes are used to estimate the contribution of terrestrial inputs along the mainstream.  相似文献   
118.
于1982年12月-1984年5月,以青岛汇泉湾习见的马粪海胆为材料,运用0.5mol/L KCl或0.5mol/L LiCl诱导法得到其卵母细胞;差速离心技术提取其线粒体;SDS萃取到线体核酸;再以羟基磷灰石柱层析分离邮线粒体核酸各组分。结果表明,从所得各种分离产物测不出任何蛋白质,所以,应用上述各种方法和技术,能够有效地分离出海胆卵母细胞线粒体中的DNA,rRNA,tRNA和多核苷酸。  相似文献   
119.
基于对胶州湾表层沉积物中总可水解氨基酸(THAA)的含量、组成、构型及分布特征的系统研究,通过氨基酸碳氮归一化产率(THAA-C%,THAA-N%)、降解因子DI、反应活性指数RI以及D型氨基酸占比(D-AA%,摩尔百分比)等指标结合碳氮比(TOC/TN)、碳稳定同位素(δ13C)探析了胶州湾沉积物中有机质的来源与降解状态,利用细菌源有机质及胞外肽酶活性(EEA)探讨了微生物在有机质迁移转化过程中的作用与贡献。结果表明,胶州湾表层沉积物中氨基酸平均含量为(7.60±3.64)μmol/g,在陆源与海源混合影响下,其水平分布呈现湾内高于湾外、湾内东部高于西部的特点,表明湾内东部陆源输入对沉积物THAA具有较高贡献。THAA-C%、THAA-N%、DI、RI以及D-AA%等指示因子均显示胶州湾表层沉积物中有机质的降解程度呈现湾外高于湾内、湾内东部高于西部的变化趋势,有机质来源、微生物活性与上覆水水深共同影响了有机质的降解程度。胶州湾表层沉积物中细菌源有机碳的贡献率为(29.35±18.73)%,其水平分布显示出湾内西部与湾外相近且高于湾内东部的特点。细菌胞外肽酶活性(EEA)平均为(0.81±1.31)nmol/(g·h)(以MCA计),整体分布趋势与细菌贡献率相反,呈现湾内东部高于湾内西部和湾外的特性。沉积物中有机质的不同海源、陆源占比决定了有机质的可降解性,而有机质的降解程度进一步影响了细菌源有机质的贡献与胞外肽酶活性。  相似文献   
120.
Global warming poses a great threat to wetland ecological stability and water quality improvement. In this paper, we sampled six types of wetlands representing different kinds of land utilisation around the TaiHu Lake Basin in southeast China. An outdoor computerized microcosm was set up in May 2008 to simulate climate scenarios of ambient temperature (control) and a warmed ambient temperature (+5 °C) using a novel minute‐scale daily and seasonal temperature manipulation technology. The 18‐month incubation indicated that warming impaired the ecological sink of sediment (fixing P from porewater) while strengthening the role of the ecological source, moreover, the rate of P release from sediment into porewater (19–113% for total phosphorus) was much stronger than from top sediment into overlying water. Warming enhanced the activity of neutral and alkaline phosphatases for P‐deficient wetland sediments and neutral phosphatases for P‐rich sediments, at the 14th month of incubation. A significant increase in total phospholipid fatty acids (PLFAs) occurred under warming in sediments with relatively low levels of PLFAs, but bacterial abundance in the sediment biomass tended to decrease (18%) along with an increase (4·5%) of the fungi‐to‐bacteria ratio. The variations of carbon consumption and availability indicated by measured dissolved organic carbon in sediment may have contributed to P release from sediments to water. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   
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