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21.
鼎湖山自然保护区大气气溶胶中的PAHs   总被引:6,自引:2,他引:6  
多环芳烃(PAHs)是环境中分布广泛、危害人类健康的有机化合物,通过对鼎湖山自然保护区自然地理和大气气溶胶中苯并(a)芘分析认为,春季样品中大气气溶胶中PAHs主要来源于高等植物排放,夏季来源于珠江三角洲经济区化石燃烧排放。  相似文献   
22.
The outer layers of layflat, low density polyethylene plastic tubing (the principal component of semi-permeable membrane devices, SPMDs) were biofouled at a clean site in Hong Kong coastal waters for periods of 1–4 weeks. Following pre-fouling, triolein was added to the SPMDs and, along with control (unfouled) devices, they were exposed to a range of organochlorine pesticides (-HCH, aldrin, p,p-DDT) and PAHs (anthracene, fluoranthene and benzo(a)pyrene) under laboratory conditions. Results showed that the uptake of contaminants by SPMDs was severely reduced by as much as 50% under fouling conditions in comparison to unfouled controls. The ultimate utility of SPMDs as passive monitors is thus reduced, although alternative measures, such as the use of permeability reference compounds may compensate, and allow for realistic evaluations of dissolved environmental concentrations in aquatic environments. However, due to the complexities involved in such procedures––especially as they need to be conducted on a case-by-case basis––the utility of SPMDs appears to be limited for estimates of bioavailability unless necessary calibrations are undertaken within each environment that the sampler is used.  相似文献   
23.
INTRODUCTIONThe Permian-Triassic ( Tr/P) boundary , datedto be (251 .4±0 .3) Ma ago ,is marked by the mostdrastic mass extinction of organisms in the Phanero-zoic .In order to explore the pattern and the cause ofthe mass extinction,extensive research has been fo-cused on biostratigraphy , isotopic chronostratigra-phy , event stratigraphy , ecostratigraphy and se-quence stratigraphy (Payne et al .,2004 ; Reichowetal .,2002 ; Yin et al .,2001 ;Jin et al .,2000 ;Zhanget al .,1996 ,1995 ;…  相似文献   
24.
傅立叶变换红外光谱联用技术在化石燃料分析中的应用   总被引:2,自引:0,他引:2  
高志农  牛菲 《岩矿测试》1998,17(1):58-63
对傅立叶变换红外光谱联用技术在化石燃料分析中的应用进行了较全面的总结评述,重点介绍了气相色谱/红外光谱联机、高压液相色谱/红外光谱联机、薄层色谱/红外光谱联机、超临界流体色谱/红外光谱联机、裂解色谱/红外光谱联机、热重分析/红外光谱联机、气相色谱/红外光谱/质谱三机联用技术等在化石燃料的结构组分分析、成因机理研究及其勘探等诸方面的重要应用,尤其是在芳香族化合物和几何异构体的分离鉴定方面发挥出的突出功效。引用文献59篇。  相似文献   
25.
Responses to abiotic and biotic stresses that potentially drive the vertical zonation of the intertidal lichens Hydropunctaria maura, an upper littoral lichen, and Wahlenbergiella mucosa, a lower littoral lichen, were investigated in field and laboratory experiments. When transplanted, both lichens exhibited an inability to survive outside their normal vertical distribution range. W. mucosa appeared to be unable to tolerate prolonged periods of desiccation following translocation from lower to upper littoral regions, whereas H. maura was unable to survive in lower littoral zones possibly owing to increased grazing pressure. The effect of desiccation in both lichens was compared using pulse amplitude modulated chlorophyll fluorescence and infra‐red gas analysis; results indicated a more hydration‐dependent nature of W. mucosa. Photosynthetic (algal) pigments and phenolic compounds were determined in both lichen thalli, and a range of additional coastal lichens occupying a natural gradient from upper to lower shore levels. Pigment composition and concentration in both lichen thalli were similar whereas levels of phenolic compounds were up to three times higher in W. mucosa than H. maura. Pigment and phenolic concentration and composition exhibited some seasonality across 13 different lichens originating from different shore levels. Phenolic concentration increased towards the lower shore, suggesting a potential anti‐herbivory function. This marks the first study of pigments and phenolics in coastal lichen communities, and prompts further investigations on the particular physiological features of marine and maritime lichens that enable them to thrive in this extreme environment.  相似文献   
26.
建立了用加速溶剂萃取,气相色谱-质谱法同时测定河流沉积物中16种多环芳烃和19种有机氯农药的分析方法,优化了萃取溶剂、萃取温度和时间、凝胶渗透色谱收集时间、固相萃取洗脱溶剂和洗脱体积等条件。16种多环芳烃的方法检出限在0.15~0.59 ng/g,加标回收率为82%~102%,相对标准偏差(RSD,n=5)为1.1%~4.5%。19种有机氯农药的方法检出限在0.14~2.23 ng/g,加标回收率为71%~108%,相对标准偏差(RSD,n=5)为1.0%~4.5%。实际样品的测定结果表明,该方法分离效果较好,能够满足沉积物样品中多环芳烃和有机氯农药的分析要求。  相似文献   
27.
利用多环芳烃标准样品连续和穿插进样相结合的方式,检验了气相色谱-燃烧-同位素比质谱仪(GC-C-IRMS)测定多环芳烃单体碳同位素比值(δ13C)的稳定性和准确性,观察了测定过程中色谱柱的分离效果。结果表明,出峰面积和分离程度是影响化合物δ13C平行性的主要原因。通过多次实验,分析了样品前处理过程中多环芳烃各个化合物稳定碳同位素的分馏情况,包括凝胶渗透色谱(GPC)和硅胶柱等净化过程,以及旋转蒸发和氮气吹扫等浓缩过程。实验表明,各前处理过程中样品内多环芳烃的稳定碳同位素分馏均不明显,其中硅胶柱净化过程相比GPC过程对样品中多环芳烃的δ13C影响较大,但总体上仍未超过未处理标样δ13C值的2倍标准偏差范围。旋转蒸发和氮吹过程对样品中多环芳烃的δ13C影响程度相当,都位于未处理标样δ13C值1倍标准偏差以内的水平。  相似文献   
28.
为了研究有机酸盐生烃演化特征,对有机酸盐进行了270℃、320℃、360℃、400℃和430℃一系列温度点的热模拟,实验结果表明,有机酸盐会大量转化为酮系列化合物,酮化合物最大产率阶段为320℃到360℃,其中360℃时产率最高,其转化率可达有机酸盐加入量的39%,400℃后产率急剧下降。这表明脂肪酸镁向酮系列化合物的最大转化温度段稍早或一致于有机质大量生烃阶段,但该类化合物对热较敏感,高温下不易保存,因此酮作为评价有机酸盐生烃贡献强度的指标只能适合于中—低温演化阶段的烃源岩。  相似文献   
29.
持久性有机污染物因其与环境和人类健康息息相关而受到国内外研究学者的持续关注。本研究以类持久性有机污染物—多环芳烃(polycyclic aromatic hydrocarbons, PAHs)和新型持久性有机污染物—六溴环十二烷(hexabromocyclododecanes, HBCDs)为研究对象,于2019年1月和2月对九龙江河口表层水体进行了采样分析,采用固相萃取 气质联用(GC MS)方法,分析其表层水体中18种溶解态多环芳烃及3种六溴环十二烷的含量分布特征和组分特征,探究其来源并进行污染评价。结果表明,表层水体中溶解态多环芳烃ΣPAHs含量范围为38.49~256.00 ng/L,各组分以2环和3环为主,4环次之,5环及以上仅有个别站位检出,其来源以石油源为主,主要来源于石油类化石燃料燃烧。HBCDs的含量范围为ND~49.951 ng/L,以α HBCD为主,γ HBCD次之,β HBCD最少。与国内外其他港湾及流域相比,九龙江河口PAHs含量依然处于较高水平,HBCDs含量则处于相对较低水平。  相似文献   
30.
南大西洋沉积物中多环芳香化合物的组成特征研究   总被引:1,自引:0,他引:1  
10 samples of sediments obtained from the South Mid-Atlantic Ridge were measured for the abundances and distributions of polycyclic aromatic compounds(PAHs). The total concentrations of PAHs(∑PAHs) ranged from 2.768 to 9.826 μg/g dry sediment. The ∑PAHs was higher in sample 22V-TVG10 and sample 26V-TVG05 which were close to hydrothermal fields, with the lowest value in sample 22V-TVG14 which was farthest from hydrothermal fields, suggesting a probable hydrothermal origin of ∑PAHs of samples. Approximately nine kinds of PAHs were identified, and low molecular mass tricyclic and tetracyclic aromatic compounds were predominant in the samples. The concentrations of fluoranthene which were typical as hydrothermal alteration compounds were the highest among PAHs with dry weight between 0.913–3.157 μg/g. The phenanthrene homologue was most abundant in the samples, and the ratios between parent phenanthrene and methylphenanthrene which probably reflected the degree of hydrothermal alteration ranged from 0.097 to 1.602. The sample 22V-TVG10 possessing a maximum ratio value showed the intense influence of the hydrothermal alteration on this sample, which might further imply that PAHs in sediments were mainly derived from the hydrothermal alteration.  相似文献   
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