全文获取类型
收费全文 | 894篇 |
免费 | 130篇 |
国内免费 | 215篇 |
专业分类
测绘学 | 6篇 |
大气科学 | 14篇 |
地球物理 | 277篇 |
地质学 | 368篇 |
海洋学 | 449篇 |
天文学 | 4篇 |
综合类 | 58篇 |
自然地理 | 63篇 |
出版年
2024年 | 4篇 |
2023年 | 17篇 |
2022年 | 35篇 |
2021年 | 44篇 |
2020年 | 41篇 |
2019年 | 50篇 |
2018年 | 40篇 |
2017年 | 34篇 |
2016年 | 34篇 |
2015年 | 41篇 |
2014年 | 52篇 |
2013年 | 73篇 |
2012年 | 43篇 |
2011年 | 79篇 |
2010年 | 36篇 |
2009年 | 69篇 |
2008年 | 55篇 |
2007年 | 59篇 |
2006年 | 52篇 |
2005年 | 44篇 |
2004年 | 43篇 |
2003年 | 27篇 |
2002年 | 40篇 |
2001年 | 30篇 |
2000年 | 31篇 |
1999年 | 21篇 |
1998年 | 20篇 |
1997年 | 20篇 |
1996年 | 22篇 |
1995年 | 16篇 |
1994年 | 9篇 |
1993年 | 14篇 |
1992年 | 10篇 |
1991年 | 9篇 |
1990年 | 1篇 |
1989年 | 2篇 |
1988年 | 2篇 |
1987年 | 2篇 |
1986年 | 1篇 |
1985年 | 5篇 |
1984年 | 6篇 |
1983年 | 3篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1976年 | 1篇 |
排序方式: 共有1239条查询结果,搜索用时 15 毫秒
61.
应用MODIS影像监测海州湾无机氮浓度的研究 总被引:1,自引:0,他引:1
利用连云港海州湾2004年至2006年的水质监测资料,选取时间上完全同步的空间分辨率为500m的MODIS Terra 1B数据,对反射率的单波段因子和波段组合因子与可溶无机氮(DIN)质量浓度之间进行相关分析。从总体上看,单波段因子与DIN质量浓度的相关性较低,但在含氮基团倍频和合频吸收带附近的波段(波段2、7)反射率与DIN质量浓度呈负相关,显示了含氮基团对水体光谱特征的影响;在波段组合因子中,因子F11(3.4)和F13(3.4)与DIN质量浓度呈显著正相关,用这两个因子建立DIN质量浓度的回归模型,R^2都达到0.7以上,相对精度达70%左右,最终选择因子F11(3.4)的线性模型反演该海域的DIN质量浓度,其结果与实际情况非常吻合。 相似文献
62.
Preliminary study on the dissolved and colloidal organic carbon in the Zhujiang River estuary 总被引:3,自引:0,他引:3
INTRODUCTIONEstuariescompriseamajorbiogeochemicalinterfaceconnectingthelandandthesea (Man toura,1 987) .Thebehaviorandfateofaparticularriver bornesubstanceintroducedintoanestuaryisdeterminedtoalargeextentbythebiogeochemicalpropertiesofthesubstanceaswellasp… 相似文献
63.
长江口盐度梯度下不同形态碳的分布、来源与混合行为 总被引:1,自引:0,他引:1
河口碳的生物地球化学过程是全球碳循环的重要组成。通过测定溶解无机碳(DIC)及其稳定同位素丰度(δ13CDIC),溶解有机碳(DOC),有色溶解有机物(CDOM),颗粒有机碳(POC)及其稳定同位素丰度(δ13CPOC)与元素比值(N/C)及相关指标,研究了2014年7月长江口盐度梯度下不同形态碳的分布、来源和混合行为。结果表明,DIC浓度、DOC浓度、POC含量分别为1 583.2~1 739.6 μmol/L,128.4~369.4 μmol/L和51.2~530.8 μmol/L,这些不同形态碳及CDOM的荧光组分的分布模式相似,均是从口内到口外,整体呈现先增大后减小的趋势,并与盐度呈现非保守混合行为。添加作用主要发生在在口门处最大浑浊带附近。与含量相反,从口内到口外,δ13CDIC和δ13CPOC均呈现逐渐减小再增大的趋势,在口门附近达到最低值,分别为-9.7‰和-26.7‰。在口门附近不同形态碳含量上升及δ13CDIC、δ13CPOC的降低可能主要与沉积物再悬浮及微生物作用有关。基于蒙特卡洛模拟的三端元混合模型的结果显示,河口内外POC来源变化明显,口内POC以陆源有机碳贡献为主,平均为62.3%,口外海源贡献逐渐增加。CDOM相关参数结果表明长江口CDOM主要来自陆源输入,海源及人类活动等也对其产生影响。 相似文献
64.
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
65.
66.
本研究利用总有机碳分析仪联用稳定同位素质谱仪(TOC-IRMS)技术,探讨了高温氧化法测试水体中溶解有机碳(Dissolved Organic Carbon, DOC)含量及稳定碳同位素组成。根据溶解有机碳的组成特征,从氧化难易程度、分子结构等方面选取5种可溶于水的化合物:咖啡因、葡萄糖、邻苯二甲酸、乙酸钾和腐殖酸钠,配置成DOC溶液。通过改变溶液碳含量、氧化温度、通氧量大小,载气流速等参数,研究不同实验条件对DOC碳转化率及δ13C值的影响。TOC-IRMS在氧化温度850℃,通氧时长20 s(流速10 cm3/min),载气流速80 cm3/min的条件下,测得5种化合物不同浓度DOC溶液的平均碳转化率为95.69%~103.57%;δ13C值与标定参考值基本一致,差值范围为-0.82‰~0.55‰。在上述实验条件下,测得不同类型水样的DOC含量相对标准偏差小于3.7%,δ13C值的标准偏差小于0.2‰,结果表明TOC-IRMS联用在线高温氧化法测定不同类型水样的DOC含量... 相似文献
67.
西北太平洋低纬度区域海水中溶解氨基酸的分布及组成研究 总被引:1,自引:1,他引:0
本文对2018年秋季西北太平洋低纬度区域上层海洋(5~200 m)中溶解氨基酸(THAA)的分布和组成进行了研究。结果表明,该海域表层海水中THAA的浓度范围为0.40~0.97μmol/L,平均浓度为0.58±0.14μmol/L;5~200m垂直断面上THAA的平均浓度为0.59±0.16μmol/L,范围为0.30~1.05μmol/L。调查海域内THAA浓度明显低于中国近海,在5~200m内的垂直分布基本表现出随深度增加而增加的趋势。将表层和垂直水体中的THAA分别与DOC、Chla等环境因子进行相关性分析,结果显示均无显著相关性。西北太平洋低纬度区域海水中的优势氨基酸是天冬氨酸(Asp)、谷氨酸(Glu)、丝氨酸(Ser)、甘氨酸(Gly)、苏氨酸(Thr)和丙氨酸(Ala)。基于氨基酸的碳归一化产率(THAA-C%)、降解因子(DI)值,表明该海域表层海水中的有机质降解程度较高,且随深度的增加而降低。 相似文献
68.
Annual Variation of Benthic Nutrient Fluxes in Shallow Coastal Waters (Gulf of Trieste, Northern Adriatic Sea) 总被引:5,自引:0,他引:5
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
69.
分别于1989年,1992年,1991年8月,1991年5月对大辽河口、鸭绿江口、滦河口、东村河口水体中总汞进行了取样和分析,其中又对大辽河口和东村河口进行了溶解态汞的分析。大辽河口和东村河口溶解态汞的含量分别为85~460ng/L和180~500ng/L,平均值分别为210和324ng/L;总汞含量分别为95~550和400~1000ng/L,平均值分别为310和640ng/L。大辽河河流段和河口段溶解态汞和颗粒态汞是主要存在形式。河口溶解态汞和颗粒态汞随氯度变化趋势相似。东村河口溶解态汞约占50%。鸭绿江口和滦河口总汞含量分别为30~2500和3700~6700ng/L,平均值分别为700和5700ng/L。鸭绿江口总汞随氯度变化趋势与随浊度变化趋势一致。而在滦河口总汞含量随两者变化趋势则不同。还讨论了滦河口、东村河口、鸭绿江口和大辽河口汞的污染程度。 相似文献
70.
Marine colloidal material (1 kDa–0.2 μm) was isolated by cross-flow ultrafiltration followed by diafiltration and freeze-drying from surface waters of the Gulf of Mexico and the Middle Atlantic Bight (MAB), as well as from estuarine waters of Galveston Bay. Elemental characterization of isolated colloidal material included organic carbon (OC) and selected trace metal (Cu, Pb, Zn, Cd, Co, Ni, Cr, Be, Fe, Al, Mn, V, Ba, and Ti) determinations. It was found that levels of these metals in marine colloids ranged from <0.1 to 50 μg/g colloidal matter, except for Fe which generally had a concentration >120 μg/g. Most metals (Cu, Pb, Zn, Ni, Al, Mn, V, and Ti) had an average concentration >1 μg/g while concentrations of Cd, Co and Be were usually <1 μg/g. Metal concentrations (μg/g) in isolated colloids were, in general, higher in Galveston Bay than in the Gulf of Mexico, suggesting either high abundance of trace metals in estuarine waters or differences in organic matter composition. Higher colloidal metal concentrations in the MAB than in the Gulf of Mexico might be due to higher terrestrial inputs in the MAB. Colloidal metal concentrations (μg/g) were generally lower than those in average soils, continental crust and suspended particles. However, metal/aluminum ratios (Me/Al) in isolated marine colloids were significantly higher than those for average soils and continental crust. Most importantly, colloids had a metal composition and metal/OC ratio (Me/C) similar to humic substances and marine plankton, suggesting that marine colloids largely originate from planktonic sources and are composed of predominately organic components. The Me/C ratios of Galveston Bay colloids followed the sequence of Cu>Ni, Cr, Zn>Mn>Co>Pb, Cd, which is similar to the Irving–Williams order except for Mn, suggesting that the interaction of metals with marine colloids is determined by the affinity of metals for specific organic ligands. 相似文献