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21.
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   
22.
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   
23.
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   
24.
气象用二等标准水银温度计检定结果不确定度分析   总被引:1,自引:1,他引:0  
温晓清  沙奕卓  雷勇 《气象科技》2008,36(2):240-243
二等标准水银温度计(简称温度计)检定结果的不确定度,直接影响温度量值传递的检定结果.针对我国省级气象计量单位现用的温度计量标准,从温度计的测温原理、检定方法、测量不确定度分量人手,根据JJFl059-1999<测量不确定度评定与表示>规范的分析方法,利用2007年检定数据,对一套温度计的检定结果进行不确定度评定.通过对检定结果的不确定度评定,梳理出一套清晰的分析步骤和科学方法,同时也为省级气象计量部门定期接受技术监督局的计量标准考核,提供误差分析范例.  相似文献   
25.
汞作为一种重要的成矿元素,广泛分布于不同地质体中,并参与成岩成矿作用.随着质谱技术的飞跃发展,汞同位素地球化学研究取得引人瞩目的进展.汞同位素被广泛地应用于示踪地球表生生物地球化学过程及汞污染等.近年来,汞同位素又被应用于揭示行星的演化过程、识别地质历史时期大火成岩省及示踪矿床成矿物质来源等方面.本文在前人研究的基础上...  相似文献   
26.
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   
27.
用巯基棉富集水中痕量汞,用饱和氯化钠的盐酸溶液解吸,冷原子吸收法测定。当水样取1 L时,最低检测浓度可达0-003 μg/L,方法相对标准偏差为3-8 % ~6-9 % ,巯基棉汞平均回收率为91-1% 。该法操作简单、快速、富集倍数大,适用于天然水中痕量汞的分析。  相似文献   
28.
种瑾  米丰收 《内陆地震》1991,5(2):155-160
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   
29.
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   
30.
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   
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