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J.P. Coelho M. Nunes M. Dolbeth M.E. Pereira A.C. Duarte M.A. Pardal 《Estuarine, Coastal and Shelf Science》2008
The annual total and organic mercury bioaccumulation pattern of Scrobicularia plana and Hediste diversicolor was assessed to evaluate the potential mercury transfer from contaminated sediments to estuarine food webs. S. plana was found to accumulate more total and organic mercury than H. diversicolor, up to 0.79 mg kg−1 and 0.15 mg kg−1 (wet weight) respectively, with a maximum annual uptake of 0.21 mg kg−1 y−1, while for methylmercury the annual accumulation was similar between species and never exceeded 0.045 mg kg−1 y−1. The higher organic mercury fraction in H. diversicolor is related to the omnivorous diet of this species. Both species increase methylmercury exposure by burrowing activities and uptake in anoxic, methylmercury rich sediment layers. Integration with the annual biological production of each species revealed mercury incorporation rates that reached 28 μg m−2 y−1, and to extract as much as 11.5 g Hg y−1 (of which 95% associated with S. plana) in the 0.4 km2 of the most contaminated area, that can be transferred to higher trophic levels. S. plana is therefore an essential vector in the mercury biomagnification processes, through uptake from contaminated sediments and, by predation, to transfer it to economically important and exploited estuarine species. 相似文献
23.
Sulfide and iron control on mercury speciation in anoxic estuarine sediment slurries 总被引:2,自引:0,他引:2
Seunghee Han Anna Obraztsova Patrizia Pretto Dimitri D. Deheyn Joris Gieskes Bradley M. Tebo 《Marine Chemistry》2008,111(3-4):214-220
In order to understand the role of sulfate and Fe(III) reduction processes in the net production of monomethylmercury (MMHg), we amended anoxic sediment slurries collected from the Venice Lagoon, Italy, with inorganic Hg and either potential electron acceptors or metabolic byproducts of sulfate and Fe(III) reduction processes, gradually changing their concentrations. Addition of sulfide (final concentration: 0.2–6.3 mM) resulted in an exponential decrease in the sulfate reduction rate and MMHg concentration with increasing concentrations of sulfide. Based on this result, we argue that the concentration of dissolved sulfide is a critical factor controlling the sulfate reduction rate, and in turn, the net MMHg production at steady state. Addition of either Fe(II) (added concentration: 0–6.1 mM) or Fe(III) (added concentration: 0–3.5 mM) resulted in similar trends in the MMHg concentration, an increase with low levels of Fe additions and a subsequent decrease with high levels of Fe additions. The limited availability of dissolved Hg, associated with sulfide removal by precipitation of FeS, appears to inhibit the net MMHg production in high levels of Fe additions. There was a noticeable reduction in the net MMHg production in Fe(III)-amended slurries as compared to Fe(II)-amended ones, which could be caused by a decrease in the sulfate reduction rate. This agrees with the results of Hg methylation assays using the enrichment cultures of anaerobic bacteria: whereas the enrichment cultures of sulfate reducers showed significant production of MMHg (4.6% of amended Hg), those of Fe(III), Mn(IV), and nitrate reducers showed no production of MMHg. It appears that enhanced Fe(III)-reduction activities suppress the formation of MMHg in high sulfate estuarine sediments. 相似文献
24.
Enhanced concentrations of dissolved gaseous mercury in the surface waters of the Arctic Ocean 总被引:2,自引:0,他引:2
During an almost three months long expedition in the Arctic Ocean, the Beringia 2005, dissolved gaseous mercury (DGM) was measured continuously in the surface water. The DGM concentration was measured using an equilibrium system, i.e. the DGM in the water phase equilibrated with a stream of gas and the gas was thereafter analysed with respect to its mercury content. The DGM concentrations were calculated using the following equation, DGM = Hgeq / kH' where Hgeq is the equilibrated concentration of elemental mercury in the gas phase and kH' is the dimensionless Henry's law constant at desired temperature and salinity. During the expedition several features were observed. For example, enhanced DGM concentration was measured underneath the ice which may indicate that the sea ice acted as a barrier for evasion of mercury from the Arctic Ocean to the atmosphere. Furthermore, elevated DGM concentrations were observed in water that might have originated from river discharge. The gas-exchange of mercury between the ocean and the atmosphere was calculated in the open water and both deposition and evasion were observed. The measurements showed significantly enhanced DGM concentrations, compared to more southern latitudes. 相似文献
25.
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
26.
文章研究了臭氧及臭氧类高级氧化技术(AOPs-O3)在不同pH条件下降解甲基对硫磷(MP)的效能。结果表明,在pH 3~10的条件下(反应过程控制pH),单独臭氧化5min即可完全降解MP,但不同pH下化学耗氧量(COD)和有机磷的释放率差异明显。在pH为3.3,7.5和9.4的条件下单独臭氧30min后COD的去除率分别为55.17%,89.64%和93.10%,有机磷的释放率分别为16.33%,95.00%和99.99%。考虑酸性条件下可以规避碳酸盐的负面影响(特别是高浓度废水),利用O3/H2O2/Ti(IV)在pH 3.3条件下处理MP溶液,COD去除率和有机磷释放率分别达到89.64%和81.57%。相对法计算求得MP与O3和羟基自由基(·OH)的速率常数分别为31.98L·(mol·s)-1和7.488×109 L·(mol·s)-1。活性污泥法的测试结果表明,MP经O3/Ti(IV)/H2O2(pH=3.3)和O3(pH=9.4)可提升含MP废水的可生化性,但与培养液体系相比仍具有一定的毒性。 相似文献
27.
利用JM—3型数字金膜测汞仪对渭河盆地活动断层进行壤中气汞测量,取得了初步结果。认为,壤中气汞异常与活动断层存在着密切的关系,通过测汞寻找隐伏活动断层,判定断层活动性是可行的。 相似文献
28.
Tang Lilian Li Fanglin 《地球科学》1986,(1)
本文以526个岩石样品的Hg、Zn测定及闪锌矿单矿物Hg的热释温度测定为基础,探讨了甲生盘层控硫铅锌矿床Hg的岩石地球化学异常特征,提出了以Hg×100/Zn为指标研究成矿后侵入体的热力对Hg的驱赶作用的可能性。从岩体向外250m的距离内,该比值逐渐从2升高到7。原生Hg异常的研究有利于解释该地壤中汞气异常的形成。已经证实,壤中汞气测量对寻找这类矿床是有效的。 相似文献
29.
Mercury in the Tinto-Odiel Estuarine System (Gulf of Cádiz, Spain): Sources and Dispersion 总被引:1,自引:0,他引:1
The Tinto and Odiel are small rivers draining one of the largest sulphide deposits in the world. As a result of these deposits and a large industrial complex, the adjacent marine area receives a high amount of metal input. Mercury distribution in the Tinto-Odiel estuary, the Huelva Ría and the Gulf of Cádiz was assessed in water and suspended particulatematter (SPM) and sediments. In the rivers and estuaries, dissolved (HgD)and particulate (HgP) mercury showed wide variations (13 to 200 pM and0.3 to 330 nmol g-1 respectively) depending on the presence or notof sulphidic waters, phosphogypsum deposits, detrital pyrite and oxyhydroxides.In the Ría, concentrations were lower than 10 pM and 4.5 nmol g-1 for HgD and HgP respectively. In surface waters of the Gulf of Cádiz, the average HgD concentration (pm standard deviation) was 2.9 pm 0.9 pM, which is similar to that of North Atlantic Central Waters. The surface sediments collected in the rivers, the Ría and the Gulf showed systematically enriched mercury compared to pre-industrial levels. Vertical mercury profiles in dated sediment cores were typical of anthropogenically influenced environments starting in the early Roman age. These distribution features suggest that most of the Hg discharged by the Huelva Ría is trapped in the sediments of the Gulf of Cádiz. 相似文献
30.