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21.
湄洲湾表层沉积物中重金属的地球化学特征 总被引:6,自引:2,他引:6
根据1984年湄洲湾表层沉积物中重金属的分析资料,讨论了它们的地球化学特征和主要来源。沉积物中重金属的含量(Fe、Mn、Cu、Ni 的质量分数均值分别为3.21%、730×10~(-6)、19.4×10~(-6)、44×10~(-6)分布比较均匀,Pb、Zn 和Co 含量(质量分数均值分别为47.0×10~(-6)、25.8×10~(-6)和243×10~(-6))偏高,微量金属含量不受Fe-Mn 氧化物和有机物控制,本地区的金属来源受陆源输入的影响明显。 相似文献
22.
Spatial and seasonal variations in depth profile of trace metals in saltmarsh sediments from Sapelo Island, Georgia, USA 总被引:1,自引:0,他引:1
This study was undertaken to elucidate the impact of early diagenetic processes on the accumulation of trace metals in Sapelo Island saltmarsh sediments as a function of time, space and sediment properties. Samples were collected from three sites in summer (May 1997) and winter (January 1998) along a transect from an unvegetated Creek Bank through a vegetated Tidal Levee to the vegetated midmarsh with evident lateral heterogeneity caused by hydrologic regime, macrophytes and microbial and macrofaunal activities. A suite of trace metals (As, Ba, Cr, Co, Cu, Cd, Mo, Ni, Pb, Th, Ti, U, V, Zn and Zr) was analyzed to obtain their depth-distribution at the three sites. Spatially marked differences were observed, that were primarily related to hydraulic flushing of trace metals away from the sites in high-energy regimes, rapid downward mixing and reworking of sediment via bioturbation, and below-ground degradation and production of Spartina biomass. Although sulfate reduction and the formation of acid volatile sulfide and pyrite were dominant processes throughout the marsh, the trace metal scavenging role of sulfides was not apparent. However, possible sulfurization of organic matter, leading to enhanced trapping of trace metals with organic carbon, may have played an important role in sequestration of trace metals.No similarity was observed visually between the depth trends of trace metals and sediment properties (grain size, iron-oxyhydroxide content, acid volatile sulfides and pyrite content) that are known to play a major role in trace metal partitioning. Only organic carbon content closely followed the trace metal profiles at all the three sites. Minor variation in depth-integrated sediment trace metal content was observed seasonally at each of the three sites. Furthermore, the depth trend of profiles of individual trace metals also did not vary significantly over the seasons either. 相似文献
23.
罗非鱼、南美白对虾对重金属富集的研究 总被引:11,自引:0,他引:11
对广东省养殖的罗非鱼Oreochromis niloticus及南美白对虾Litopeneaus vannamei体内Pb、Cd、Hg、As 4种重金属富集及分布状况进行研究。比较了不同规格罗非鱼及南美白对虾体内重金属差异。分析重金属在罗非鱼及南美白对虾不同部位的分布状况。结果表明,罗非鱼及南美白对虾体内Pb、Cd、Hg、As均有不同程度的检出,但含量均低于国家限定标准(NY5125-2002);其中Pb的含量最高,罗非鱼和南美白对虾体内Pb含量最高值分别为限量的39.32%和42.18%;重金属含量因其规格大小及部位而异,趋势为大规格样品重金属含量相对较高,重金属含量在罗非鱼及南美白对虾体内的增长情况与其体重具有正相关性;罗非鱼内脏重金属含量明显高于肌肉组织,虾头为虾重金属富集的主要部位。 相似文献
24.
原子吸收光谱法和等离子光谱法分别研究了潮滩盐沼植物翅碱蓬(Suaedaheterop-tera)根际与非根际(根上部和根下部)沉积物中Cu、Zn、Pb和Cd的总量和化学形态。结果表明,从总量来看,不同潮滩沉积物中4种重金属次序均为Zn>Pb>Cu>Cd,但同一元素随潮滩位置变化明显,尤以中潮滩差异最显著,重金属总量明显大于其他两个潮滩(低潮滩和高潮滩),特别是根际沉积物中的重金属总量远高于非根际沉积物总量,其比值分别为Cu3·4—4·2倍,Zn2·2—2·7倍,Pb3·2—3·3倍。同一潮滩均表现为根际沉积物>根上部>根下部。Cd含量相对较低,其变化不明显。从化学形态看,沉积物重金属表现为环境直接影响态(交换态和有机结合态)、环境间接影响态(碳酸盐态和铁锰氧化物态)和稳定态(残渣态)。与非根际沉积物相比,根际沉积物中重金属的化学形态发生了显著的变化,Cu和Pb以稳定态为主,其次为环境间接影响态,环境直接影响态最低;Zn与上述2种金属不同,以环境直接影响态含量最高(可交换态是有机结合态的7倍),其次分别为环境间接影响态(主要是碳酸盐结合态)和稳定态。实验结果表明,由于特异根圈效应,一方面该植物使可迁移形态的Cu和Pb在根际逐步得到矿化,使其生物可利用性降低;另一方面使Zn的生物可利用性提高,促进了植物对Zn的吸收利用。 相似文献
25.
大窑湾疏浚物倾倒区环境调查研究 总被引:2,自引:1,他引:2
本文以1989年8月调查资料为基础,论述了大窑湾疏浚物倾倒区的水化学要素(pH、盐度、DO、COD、浊度)、营养盐(NO_2-N、NO_3-N、NH_4-N、PO_4-P、SiO_3-Si)和重金属(Cu、Zn、Pb、Cd)等污染物分布特征;分析了水质、底质的环境状况及潮流的影响。从环境地球化学观点探讨了该疏浚物倾倒区选择的科学性。 相似文献
26.
27.
Cu2+、Zn2+、SDS、DBS对脊尾白虾的毒性试验 总被引:4,自引:0,他引:4
选用铜、锌2种常见重金属和十二烷基硫酸钠(SDS)、十二烷基苯磺酸钠(DBS)2种阴离子表面活性剂对脊尾白虾Palaemon carincauda仔虾进行96h急性毒性试验。结果表明,Cu2 、Zn2 、SDS、DBS对脊尾白虾仔虾的96h LC50分别为0.34、0.82、14.3和14.4 mg.L-1。将脊尾白虾仔虾对这4种毒物的敏感性与文献报道的其它动物进行了比较,结果认为可以将其作为毒性测试的标准试验生物。 相似文献
28.
29.
Determination of cadmium(II), copper(II), manganese(II) and nickel(II) species in Antarctic seawater with complexing resins 总被引:1,自引:0,他引:1
Raffaela Biesuz Giancarla Alberti Girolamo D'Agostino Emanuele Magi Maria Pesavento 《Marine Chemistry》2006,101(3-4):180-189
The strong species of cadmium(II), copper(II), manganese(II) and nickel(II) in an Antarctic seawater sample are investigated by a method based on the sorption of metal ions on complexing resins. The resins compete with the ligands present in the sample to combine with the metal ions. Two resins with different adsorbing strengths were used. Very stable metal complexes were investigated with the strong sorbent Chelex 100 and weaker species with the less strong resin, Amberlite CG-50. Strong species were detected for three of the considered metal ions, but not for Mn(II). Cu(II) is completely linked to species with a side reaction coefficient as high as log αM(I) = 11.6 at pH = 7.3. The ligand concentration was found to be similar to that of the metal ion, and the conditional stability constant was around 1020 M− 1. In the considered sample, only a fraction of the metal ions Cd(II) and Ni(II) is bound to the strong ligands, with side reaction coefficients equal to log αM(I) = 5.5 and 6.5 at pH = 7.3 for Cd(II) and Ni(II), respectively. These findings were confirmed by the test with the weaker sorbent Amberlite CG-50. It can be calculated from the sorption equilibria that neither Mn(II) nor Ni(II) is adsorbed on Amberlite CG-50 under the considered conditions and, in fact, only a negligible fraction of Mn(II) and Ni(II) was adsorbed. A noticeable fraction of Cd(II) was adsorbed on Amberlite CG-50, meaning that cadmium(II) is partially linked to weak ligands, possibly chloride, while no copper(II) was adsorbed on this resin, confirming that copper(II) is only combined in strong species. These results are similar, but not identical, to those obtained for other seawater samples examined in previous investigations. 相似文献
30.