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101.
Katsumi Matsumoto 《Journal of Oceanography》2006,62(6):887-902
Iron fertilization of nutrient-rich surface waters of the ocean is one possible way to help slow the rising levels of atmospheric
CO2 by sequestering it in the oceans via biological carbon export. Here, I use an ocean general circulation model to simulate
a patch of nutrient depletion in the subpolar northwest Pacific under various scenarios. Model results confirm that surface
fertilization is an inefficient way to sequester carbon from the atmosphere (Gnanadesikan et al., 2003), since only about 20% of the exported carbon comes initially from the atmosphere. Fertilization reduces future production
and thus CO2 uptake by utilizing nutrients that would otherwise be available later. Effectively, this can be considered as leakage when
compared to a control run. This “effective” leakage and the actual leakage of sequestered CO2 cause a significant, rapid decrease in carbon retention (only 30–45% retained after 10 years and less than 20% after 50 years).
This contrasts markedly with the almost 100% retention efficiency for the same duration using the same model, when carbon
is disposed directly into the northwest Pacific (Matsumoto and Mignone, 2005). As a consequence, the economic effectiveness
of patch fertilization is poor in two limiting cases of the future price path of carbon. Sequestered carbon in patch fertilization
is lost to the atmosphere at increasingly remote places as time passes, which would make monitoring exceedingly difficult.
If all organic carbon from one-time fertilization reached the ocean bottom and remineralized there, acidification would be
about −0.05 pH unit with O2 depletion about −20 μmol kg−1. These anomalies are probably too small to seriously threaten deep sea biota, but they are underestimated in the model because
of its large grid size. The results from this study offer little to advocate purposeful surface fertilization as a serious
means to address the anthropogenic carbon problem. 相似文献
102.
103.
Rapid economic developments in East Asian countries have inevitably resulted in environmental degradation in the surrounding seas, and concern for both the environment and protection from pollutants is increasing. Identification of sources of contaminants is essential to environmental pollution management. In this study, the provenance of anthropogenic lead (Pb), a major pollutant of Yellow Sea sediments, was determined for river mouth sediments, including those of the Changjiang, Huanghe, Han, and Geum Rivers, and for age-determined shelf core sediments through the measurement of Pb isotope ratios in the HCl-leached fraction using multi-collector inductively coupled plasma-mass spectrometry (MC ICP/MS). Anthropogenic Pb has accumulated in shelf core sediments since 1910, and its isotope ratios were estimated as 0.863–0.866 and 2.119–2.125 for 207Pb/206Pb and 208Pb/206Pb, respectively, from the mixing relationships of the two endmembers. River mouth sediments exhibited enough distinction in anthropogenic Pb isotope ratios to be discriminated: 0.874 (2.144) in the Huanghe, 0.856 (2.129) in the Han, 0.857 (2.122) in the Geum, and 0.854 (2.101) in the Changjiang for 207Pb/206Pb (208Pb/206Pb), respectively. Although isotope ratios of geogenic Pb in sediments dating before 1910 showed narrow ranges (0.842–0.845 and 2.088–2.100 for 207Pb/206Pb and 208Pb/206Pb, respectively), distinct isotope ratios in each core permitted source identification of sediments in the Yellow Sea based on geographic locations and the geogenic Pb of each river. By comparing the isotope ratios of the estimated anthropogenic Pb to source-related materials, the provenances of anthropogenic Pb in Chinese river sediments were presumed to be Chinese coal or ore, which is also a major source of atmospheric particulate Pb. The anthropogenic Pb in the shelf core sediments in the northern Yellow Sea originated from northern Chinese cities such as Beijing and Tianjin through atmospheric pathways. Pb isotope ratios indicated that Pb in Korean river sediments was characteristic of local Korean ores. 相似文献
104.
秋茄和榕树叶片中正构烷烃分布和单体化合物δ13C值及其光合作用 总被引:1,自引:0,他引:1
对深圳福田、阳江、海南新竹红树林秋茄Kandelia candel及海口榕树Ficusm icrocarpa叶中类脂物进行萃取,分离出正构烷烃,通过气相色谱(GC)及色谱-质谱(GC MS)分析,测出了正构烷烃的碳数分布和相对含量.气相色谱-稳定同位素比质谱仪(GC-IRMS)测定了正构烷烃单体化合物的稳定同位素组成δ13C.秋茄叶和榕树叶正构烷烃的碳数分布均为C17C33,主要集中在C23-C31(>90%).化合物含量最高为C27的有深圳福田秋茄、海南新竹秋茄、海口榕树,而阳江秋茄为C25.单体化合物的稳定同位素δ13C深圳福田秋茄为-31.42‰-34.48‰,阳江秋茄为-31.69‰-33.62‰,海南新竹秋茄为-30.30‰-33.04‰,海口榕树为-29.92‰33.56‰;平均值分别为-32.95‰、32.67‰、31.67‰、-31.74‰.结果表明,秋茄和陆地植物榕树的光合作用都是通过C3途径,是典型C3植物. 相似文献
105.
渐新世/中新世分界的地层学事件 总被引:5,自引:1,他引:5
介绍渐新世/中新世分界面(即古近纪/新近纪分界面)附近的浮游有孔虫和钙质超微化石事件及其新年龄。2004年国际地层年代表确定该分界面位于第58长偏心率周期弱振幅处,古地磁事件C6Cn.2n底面,经天文调谐后的年龄为23.03 Ma。发生在该界面附近的生物地层学事件主要是浮游有孔虫Paragloborotalia kugleri的始现面(22.96 Ma)和钙质超微化石Sphenolithus delphix的末现面(23.11 Ma)。在南海北部东沙群岛附近的大洋钻探ODP1148站,渐新世/中新世界面以崩塌沉积物为特征,有明显沉积间断,标志南海当时有较大范围的构造运动。 相似文献
106.
分析了赤道东北太平洋海域沉积物中Ba、Ti、Al和有机碳(Corg)的含量。研究表明,研究区沉积物中钡为0.198%~0.792%;采用标准陆源物质扣除法获得的生物钡(Babio)的含量为0.162%~0.764%,占沉积物中总钡含量的81.6%~96.5%,平均为88.7%,其在沉积物中的分布表现为上部一致,下部变化较大;有机碳(Corg)的含量为0.18%~0.58%,并表现为随沉积物深度的增加而降低。沉积物中Babio/Ti的比值表现为东区高于西区,且向高纬度降低的特点,而沉积物中Corg/Ti和Babio/Ti则表现为负相关关系,表明研究区沉积物中钡可能和上层海洋生产力的相关性不明显。 相似文献
107.
108.
The common assumption that the ratio between particulate organic carbon (POC) and particulate 234Th obtained from shallow sediment traps and filterable particles are representative of the ratio in the total particle settling flux should be treated with caution in view of well-known biases associated with tethered shallow sediment traps and the decoupling between size and settling velocity of many natural particle regimes. To make progress toward reliably constraining the POC / 234Th ratio on truly settling particles, we have tested here a settling collection technique designed to remove any hydrodynamic bias; split flow-thin cell fractionation (SPLITT). These first results from a North Sea fjord and an open Baltic Sea time-series station indicates that the POC / 234Th ratio on the more complete particle-settling spectrum, isolated with SPLITT, was higher than the POC / 234Th ratio obtained simultaneously from tethered shallow sediment traps in seven out of seven parallel deployments with an average factor of 210%. The POC / 234Th ratio from the SPLITT was either in the same range or higher than that obtained on filtered “bulk” particles. To explain this novel data we hypothesize that the slowest settling fraction is organic-matter rich and does not strongly complex 234Th (i.e., high POC / 234Th). We suggest that this ultra-slow sinking fraction is better collected by SPLITT than with tethered sediment traps because of minimized hydrodynamic bias.This was tested using the ratio of POC / Al as a tracer of detrital mineral-ballast influenced settling velocity. The higher POC / Al ratios in SPLITT samples relative to in traps is consistent with the hypothesis that SPLITT is better suited for collecting also the slow-settling component of sinking particles. This important slow-settling component appears to here consist primarily of non-APS/TEP components of plankton exudates or other less-strongly 234Th-complexing organic matter. Further applications of the SPLITT technique are likely to return increasingly new insights on the composition (including “truly settling” POC / 234Th) of the total spectrum of particles settling out of the upper ocean. 相似文献
109.
The physical and chemical variability of the water column at subtidal station of an estuary in the Seto Inland Sea, Japan,
was studied over a 24-hour period during a spring tide (tidal range ca. 2 m) in May 1995. Surface water and several depths through the water column were monitored every one and two hours, respectively.
At each occasion, water temperature, salinity and dissolved oxygen concentration were measured and water samples were collected
for the determination of nutrients and suspended particulate matter (SPM). Disruptive changes in the physical and chemical
characteristics of the water was produced by the tidal cycle and the mixing of water masses of different origin. These changes
were highly significant both spatially and temporally, yet with varying effects on physical parameters, nutrients and the
different components of SPM. Significant differences in nutrient concentrations were also observed when the data-set was divided
into ebb and flood components, irrespective of the depth. Nitrate and nitrite rose to 1.8 times higher during the flood. Spatial
differences of SPM were less marked than those of nutrients, only particulate organic carbon (POC) being significantly higher
at the surface than in the intermediate and the lower layer. Both POC and pheopigment concentrations increased markedly through
the water column, being highest shortly before the lower low tide. In contrast, suspended solid (SS) content increased sharply
after the lower low tide (>40 mg l−1) and this coincided with a marked decrease of the C/SS content (<20 mg g−1). The lagtime between POC and SS tidal transport was caused by particle resuspension from the exposed intertidal sediments
as the tidal level rose, and particle transport selection in relation to the tidal state.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
110.
气象要素与蒸发密切相关,通过室内外不同气象条件下的器皿水蒸发实验,获得了水面蒸发氢氧稳定同位素分馏因子与气象要素的关系。实验结果表明,随着蒸发的进行,剩余水体中逐渐富集重同位素;自由水体蒸发同位素分馏在垂线上有分层现象,表层水体同位素值比垂线平均的同位素值略富集;不同温度条件下的室内蒸发实验中,温度越高,液-气间分馏系数越小,相应于同一剩余水体体积比,剩余水体稳定同位素值则越低。室外器皿水自由蒸发实验中得出的蒸发线方程斜率较大地偏离了当地降水线,表明实验期间水体蒸发分馏作用较明显。该研究为进一步揭示水体蒸发分馏规律提供了可靠的实验依据。 相似文献