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221.
岩溶区地下水补给型水库表层无机碳时空变化特征及影响因素 总被引:6,自引:2,他引:4
为更深入地认识岩溶区地下水补给型水库表层无机碳的循环过程,于2014-07-12~2014-07-20期间,以广西上林县大龙洞岩溶水库表层水体为研究体系,对无机碳循环研究的重要指标进行定点观测和高密度的昼夜监测.结果发现:1从上游到下游DIC含量和水体p CO2值逐渐增加[DIC(平均):122.88 mg·L-1增至172.02 mg·L-1,p CO2(平均):637.91×10-6增至1 399.97×10-6],δ13CDIC值逐渐偏负[δ13CDIC(平均):-4.34‰降至-6.97‰].2库区均为大气CO2的源,CO2交换通量在7.11~335.54 mg·(m2·h)-1之间,平均125.03 mg·(m2·h)-1,上游和下游地区CO2交换通量较大[平均131.73 mg·(m2·h)-1、170.25 mg·(m2·h)-1],中游狭窄地区CO2交换通量较小[平均116.05 mg·(m2·h)-1].3表层水体p CO2值和水-气界面CO2交换通量存在晚上升高,白天降低的昼夜变化规律,且与叶绿素a(Chla)呈负相关关系.分析认为:1大龙洞水库表层水体DIC含量、δ13CDIC值和水体p CO2的空间分布主要受浮游植物浓度、浊度、电导率、水深、透明度等的影响,而水-气界面CO2交换通量除了受浮游植物浓度空间变化的影响外还受风速的影响.2浮游植物昼夜垂向运动及光合作用和呼吸作用昼夜变化控制着水库表层水体溶解性无机碳的昼夜循环过程. 相似文献
222.
对贵州施秉白云岩喀斯特世界自然遗产地49个水点进行采样,分析地表水和地下水水化学特征及控制因素,并探讨溶解无机碳(DIC)稳定同位素的分布特征和来源.结果发现,研究区地表水和地下水p H值呈中性到碱性,溶解质较低,水中阳离子以Ca2+、Mg2+为主,阴离子以HCO-3为主,水化学类型为重碳酸-钙镁型(HCO3-Ca·Mg).北部上游页岩分布区外源水水中Cl-、NO-3、SO2-4的比重相对白云岩区喀斯特水水点的高,Si的含量也明显高于白云岩地区喀斯特水;外源水的SIc和SId值为负,而流经白云岩区后均大于0.水化学数据表明研究区水化学受降水和人为活动影响很小,Gibbs图显示水中离子组成主要受岩性的控制.研究区喀斯特地表水中δ13CDIC值变化范围为-8.27‰~-11.55‰,平均为-9.45‰,地下水的δ13CDIC值范围为-10.57‰~-15.59‰,平均为-12.04‰,地表水δ13CDIC值比地下水偏重.DIC的δ13CDIC值在杉木河支流上整体表现为河流上游相对于下游偏轻,而杉木河干流上河水DIC的δ13CDIC值的变化则比较复杂.根据同位素质量平衡,利用DIC的δ13CDIC实测值,计算了喀斯特区地下水DIC来自土壤CO2和白云岩矿物溶解的比例,计算结果为51.2%来自于土壤CO2,矿物本身的贡献约为48.8%. 相似文献
223.
硫氧同位素示踪南京北郊大气PM2.5中硫酸盐来源 总被引:3,自引:1,他引:2
采用EA-IRMS联用技术对2014年1月南京北郊大气细粒子(PM2.5)中硫酸盐的硫和氧同位素组成进行了分析,结合大气颗粒物化学组成,追溯南京北郊大气PM2.5中硫酸盐的来源,并评估了各污染源的贡献率.结果表明,2014年1月南京北郊硫酸盐气溶胶的硫同位素组成(δ34S)范围为2.7‰~6.4‰,平均值为5.0‰±0.9‰(n=16);氧同位素组成(δ18O)值范围为10.6‰~16.1‰,平均值为12.5‰±1.37‰(n=16).通过气溶胶与可能污染源的δ34S值对比和后向轨迹分析,得出结论:研究区域大气中硫同位素组成主要受当地燃煤中硫的影响,其次是远距离传输硫.此外,有低δ34S值硫源存在,但贡献比较小,可能来自生物成因硫.绝对主因子分析结果显示:人为成因硫和远距离传输硫贡献率分别为46.74%和31.54%. 相似文献
224.
225.
ABSTRACT: Stable isotopes of deuterium and oxygen-18 of surface and ground water, together with anion concentrations and hydraulic gradients, were used to interpret mixing and flow in ground water impacted by artificial recharge. The surface water fraction (SWF), the percentage of surface water in the aquifer impacted via recharge, was estimated at different locations and depths using measured deuterium/hydrogen (DIH) ratios during the 1992, 1993, and 1994 recharge seasons. Recharged surface water completely displaced the ground water beneath the recharge basins from the regional water table at 7.60 m to 12.16 m below the land surface. Mixing occurred beneath the recharge structures in the lower portions of the aquifer (>12.16 m). Approximately 12 m down-gradient from the recharge basin, the deeper zone (19.15 m depth) of the primary aquifer was displaced completely by recharged surface water within 193, 45, and 55 days in 1992, 1993, and 1994, respectively. At the end of the third recharge season, recharged surface water represented ~50 percent of the water in the deeper zone of the primary aquifer ~1000 m downgradient from the recharge basin. A classic asymmetrical distribution of recharged surface water resulted from the recharge induced horizontal and vertical hydraulic gradients. The distribution and breakthrough times of recharged surface water obtained with stable isotopes concurred with those of major anions and bromide in a tracer test conducted during the 1995 recharge season. This stable isotope procedure effectively quantified mixing between surface and ground water. 相似文献
226.
227.
Woo-Jung Choi Gwang-Hyun Han Sang-Mo Lee Goon-Taek Lee Kwang-Sik Yoon Soo-Myung Choi Hee-Myong Ro 《Agriculture, ecosystems & environment》2007,120(2-4):259-268
An understanding of the long-term changes in the nitrate contamination pattern of unconfined groundwater is critical to conservation of drinking water in rural areas supporting mixed land-use activities such as cropping, livestock farming, and residence. To examine the effect of different land-use activities on nitrate contamination, groundwater samples were collected monthly for 3 years (1997–1999) from 12 wells in rural areas with different land-use activities and analyzed for the concentrations and N isotopic ratios (δ15N) of nitrate. The characteristics of nitrate contamination clearly differed with land-use activities. The percentages of samples that had a nitrate concentration exceeding the national standard for drinking water (10 mg N L−1) were 0, 23, 43, and 67% for the uncontaminated natural area, cropping area, cropping-livestock farming complex area, and residential area, respectively. The range of δ15N values was between +1.4 and +4.5‰ for groundwater nitrate from the uncontaminated natural area. In the cropping area, the δ15N values were slightly different with the type of fertilizer applied to fields in the vicinity of the well, and the values ranged between +8.7 and +14.4‰ for the compost-applied area and between +4.5 and +8.5‰ for the area where urea was applied with compost. The δ15N values of the cropping-livestock farming complex area ranged from +1.0 to +17.7‰, probably resulting from mixed contamination sources (inorganic fertilizer and livestock manure). The well located closest to the livestock feedlot had relatively higher δ15N values, with a range between +8.7 and +17.6‰. In the residential area, a higher δ15N (most frequently above +10‰) of nitrate suggested that the major source of contamination was effluent from leaky septic tanks. Our data showed that unconfined groundwater is susceptible to land-use activities above the aquifers, and the impacts of the activities could be more precisely inferred from long-term data on the concentration and δ15N of nitrate. By determining the impacts, more effective (specific to contamination sources) measures for preventing groundwater quality could be implemented. 相似文献
228.
William C. Sidle 《Journal of the American Water Resources Association》2003,39(5):1067-1077
ABSTRACT: Water balance modeling and the analysis of stable water isotopes in ground water were conducted to aid the location of ground water discharge areas within the Goose River basin, in mid‐coastal Maine. Previous investigations of drinking water from wells in the fractured crystalline bedrock encountered persistent elevated total arsenic. Such contamination may be related to discharging ground water from fractured zones in the basin. Modeled discharge rates greater than +10 cm/yr and 18O values lighter than‐9.5 per mil VSMOW may indicate recent recharge is mixing with deeper ground water and is focused along some fractured zones in arsenic bearing crystalline rocks. 相似文献
229.
上海市大气气溶胶中铅污染的综合研究 总被引:14,自引:2,他引:12
采用质子激发X荧光分析(PIXE)、质子微探针、电感耦合等离子质谱(ICP-MS)和扩展X-射线吸收精细结构谱(EXAFS)等分析手段研究上海市大气气溶胶PM10中铅的浓度、化学种态和铅的源解析.研究发现2002年冬天和2003年上海地区大气气溶胶PM10中铅的平均浓度分别为369ng/m3和224ng/m3,铅的化学种态主要是PbCl2、PbSO4和PbO,燃煤烟尘、钢铁烟尘和汽车尾气是主要排放源,它们对气溶胶中铅的贡献率分别为50%、35%和15%. 相似文献
230.