首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   318篇
  免费   66篇
  国内免费   75篇
测绘学   1篇
大气科学   51篇
地球物理   121篇
地质学   117篇
海洋学   114篇
综合类   18篇
自然地理   37篇
  2024年   1篇
  2023年   7篇
  2022年   12篇
  2021年   22篇
  2020年   18篇
  2019年   13篇
  2018年   13篇
  2017年   12篇
  2016年   13篇
  2015年   16篇
  2014年   15篇
  2013年   34篇
  2012年   15篇
  2011年   12篇
  2010年   20篇
  2009年   14篇
  2008年   15篇
  2007年   23篇
  2006年   28篇
  2005年   18篇
  2004年   14篇
  2003年   16篇
  2002年   13篇
  2001年   10篇
  2000年   14篇
  1999年   15篇
  1998年   10篇
  1997年   8篇
  1996年   6篇
  1995年   3篇
  1994年   1篇
  1993年   6篇
  1992年   4篇
  1991年   1篇
  1990年   3篇
  1989年   2篇
  1988年   2篇
  1987年   2篇
  1986年   2篇
  1985年   3篇
  1984年   1篇
  1983年   1篇
  1981年   1篇
排序方式: 共有459条查询结果,搜索用时 298 毫秒
21.
喀斯特适生植物固碳增汇策略   总被引:5,自引:1,他引:4  
吴沿友 《中国岩溶》2011,30(4):461-465
通过分析喀斯特地区的土壤化学性质,明确了喀斯特地区植物的固碳增汇的限制因素为岩溶干旱、低营养、高pH、高重碳酸盐等。通过对喀斯特适生植物和非适生植物的无机碳源、氮源的利用以及对低营养的响应差异分析,总结出了喀斯特适生植物交替、高效利用碳酸氢根离子作碳源的开源固碳增汇策略,以较低的营养成本获取较高的光合固碳能力的低成本倍增固碳增汇策略,以及掠夺式吸收限制性的铵态氮和补偿式吸收硝态氮来实现固碳增汇作用的以氮增汇策略等;提出了喀斯特适生植物固碳增汇能力的利用途径,可最大限度挖掘出喀斯特地区植物的固碳增汇潜能。   相似文献   
22.
三峡库区梁滩河流域水化学与硝酸盐污染   总被引:9,自引:1,他引:8  
运用水化学和水质分析技术,测定了三峡库区梁滩河流域地表水体和地下水体中的水化学组成和硝酸盐氮含量,揭示了梁滩河流域地表水和地下水水体的水化学组成和硝酸盐污染的空间分布规律、来源及循环过程。结果表明:梁滩河流域地表水的硝酸盐污染表现为沿着地表径流从上游到下游呈现出加重的趋势,这种污染趋势与养殖业、生活和工农业废污水的沿程直接排放有着直接关系;而地下水硝酸盐污染呈现出流域上游和下游较轻、而中游东侧支流区域较重的空间分布特征,这种空间分布特征与地表水体中氨氮和有机氮的含量、地表水与地下水之间的补给排泄关系、厚层土壤包气带的存在以及土地利用状况等因素有着密切的关系。  相似文献   
23.
针对复杂硝酸铵水盐体系溶解度的测定,传统分析方法操作步骤繁琐,且试剂较贵,引入一种简单准确的分析方法,即热分解法,对LiNO3-KNO3-NH4NO3-H2O体系和NaNO3-KNO3-NH4NO3-H2O体系中硝酸铵和水的含量进行精确分析。结果表明,热分解温度控制在230~240℃,若控制样品质量为1.5 g,分解时间不低于36 h,能将LiNO3-KNO3-NH4NO3-H2O体系中的硝酸铵和水彻底分解,且随着样品中硝酸铵含量增加,热分解时间也将延长,分析相对误差能控制在0.2%以内。针对复杂NaNO3-KNO3-NH4NO3-H2O体系,热分解温度控制在230~255℃,若控制样品质量为1.5 g,分解时间不少于44 h,且随着样品中硝酸铵含量的增加,相应延长热分解时间,能将复杂NaNO3-KNO3-NH4NO3-H2O体系中的硝酸铵和水彻底分解,分析相对误差能控制在0.2%以内。  相似文献   
24.
The hyporheic zone of riverbed sediments has the potential to attenuate nitrate from upwelling, polluted groundwater. However, the coarse‐scale (5–10 cm) measurement of nitrogen biogeochemistry in the hyporheic zone can often mask fine‐scale (<1 cm) biogeochemical patterns, especially in near‐surface sediments, leading to incomplete or inaccurate representation of the capacity of the hyporheic zone to transform upwelling NO3?. In this study, we utilised diffusive equilibrium in thin‐films samplers to capture high resolution (cm‐scale) vertical concentration profiles of NO3?, SO42?, Fe and Mn in the upper 15 cm of armoured and permeable riverbed sediments. The goal was to test whether nitrate attenuation was occurring in a sub‐reach characterised by strong vertical (upwelling) water fluxes. The vertical concentration profiles obtained from diffusive equilibrium in thin‐films samplers indicate considerable cm‐scale variability in NO3? (4.4 ± 2.9 mg N/L), SO42? (9.9 ± 3.1 mg/l) and dissolved Fe (1.6 ± 2.1 mg/l) and Mn (0.2 ± 0.2 mg/l). However, the overall trend suggests the absence of substantial net chemical transformations and surface‐subsurface water mixing in the shallow sediments of our sub‐reach under baseflow conditions. The significance of this is that upwelling NO3?‐rich groundwater does not appear to be attenuated in the riverbed sediments at <15 cm depth as might occur where hyporheic exchange flows deliver organic matter to the sediments for metabolic processes. It would appear that the chemical patterns observed in the shallow sediments of our sub‐reach are not controlled exclusively by redox processes and/or hyporheic exchange flows. Deeper‐seated groundwater fluxes and hydro‐stratigraphy may be additional important drivers of chemical patterns in the shallow sediments of our study sub‐reach. © 2015 The Authors. Hydrological Processes Published by John Wiley & Sons Ltd.  相似文献   
25.
用θ~θ液体衍射仪精确测量了Ca(NO3)2.4H2O熔体的X射线衍射数据,通过数据处理给出了熔盐的结构函数和实验径向分布函数曲线,并由r=0.618λ/sinθ对结构函数曲线进行了定性描述;通过理论模型计算获得了熔体配位结构参数。研究结果表明,熔体中至少存在一种带单氧桥键或双氧桥键的双核配合物;并用计算给出的局域结构模型,讨论了熔体结构对晶体生长过程的影响。  相似文献   
26.
根据2010年5月至2010年10月每月对青木关地下河河水的监测数据,利用15N同位素技术并结合水化学指标,分析地下河的水化学特征以及硝态氮来源的时空变化特征。结果表明,地下河出口丁家龙洞硝态氮浓度(5.077mg/L)比入口天池硝态氮浓度(0.842mg/L)高6倍多。入口天池处地下河河水硝态氮浓度比较低,δ15N浓度变化范围为-7.0475‰~+7.059‰,变化幅度不大,说明该点的氮污染较低,地下水受外界影响较小,污水和粪便不是主要的δ15N来源。出口丁家龙洞处的δ15N浓度变化范围在-21.453‰~+37.825‰,总体浓度高且变化幅度大,受上游养猪场粪便直接排入及降水影响较大。   相似文献   
27.
本文采用石墨炉原子吸收光谱法测定地球化学样品中痕量银。选择硝酸镁和硫脲混合溶液为基体改进剂,银的灰化温度为800℃,研究了最佳的分析测定条件。该方法检出限为0.01μg/g。用该方法对国家地球化学标准样品的测定结果与标准值相符。  相似文献   
28.
实验研究了4A沸石分子筛经熔融盐处理后对KNO3和NH4NO3的吸持作用。结果表明:在实验条件下,KNO3处理后的4A沸石中含钾(以K2O计)15.01%,含NO-3 9.23%;NH4NO3处理后的4A沸石中含NO-3 10.78%,含NH+4 0.94%。熔融盐处理后的样品X射线衍射峰相对强度发生了变化,红外光谱中1 640 cm-1附近水的吸收带强度减弱,1 390 cm-1附近出现的NO-3离子的强吸收带及825 cm-1附近出现的NO-3离子的弱吸收带,以及热重-差热曲线中KNO3和NH4NO3的热失重和分解热效应均证明沸石中吸持盐的存在。处理后4A沸石分子筛的基本骨架结构没有被破坏,吸持盐的4A沸石对营养盐的储备大大提高,是潜在的缓释肥料。  相似文献   
29.
The southwestern Adirondack region of New York receives among the highest rates of atmospheric nitrogen (N) deposition in the USA. Atmospheric N deposition to sensitive ecosystems, like the Adirondacks, may increase the acidification of soils through losses of exchangeable nutrient cations, and the acidification of surface waters associated with enhanced mobility of nitrate (NO3?). However, watershed attributes, including surficial terrestrial characteristics, in‐lake processing, and geological settings, have been found to complicate the relationships between atmospheric N deposition and N drainage losses. We studied two lake‐watersheds in the southwestern Adirondacks, Grass Pond and Constable Pond, which are located in close proximity (~26 km) and receive similarly high N deposition, but have contrasting watershed attributes (e.g. wetland area, geological settings). Since the difference in the influence of N deposition was minimal, we were able to examine both within‐ and between‐watershed influences of land cover, the contribution of glacial till groundwater inputs, and in‐lake processes on surface water chemistry with particular emphasis on N solutes and dissolved organic carbon (DOC). Monthly samples at seven inlets and one outlet of each lake were collected from May to October in 1999 and 2000. The concentrations of NO3? were high at the Grass Pond inlets, especially at two inlets, and NO3? was the major N solute at the Grass Pond inlets. The concentrations of likely weathering products (i.e. dissolved Si, Ca2+, Mg2+, Na+) as well as acid neutralizing capacity and pH values, were also particularly high at those two Grass Pond inlets, suggesting a large contribution of groundwater inputs. Dissolved organic N (DON) was the major N solute at the Constable Pond inlets. The higher concentrations of DON and DOC at the Constable Pond inlets were attributed to a large wetland area in the watershed. The DOC/DON ratios were also higher at the Constable Pond inlets, possibly due to a larger proportion of coniferous forest area. Although DON and DOC were strongly related, the stronger relationship of the proportion of wetland area with DOC suggests that additional factors regulate DON. The aggregated representation of watershed physical features (i.e. elevation, watershed area, mean topographic index, hypsometric‐analysis index) was not clearly related to the lake N and DOC chemistry. Despite distinctive differences in inlet N chemistry, NO3? and DON concentrations at the outlets of the two lakes were similar. The lower DOC/DON ratios at the lake outlets and at the inlets having upstream ponds suggest the importance of N processing and organic N sources within the lakes. Although an inverse relationship between NO3? and DOC/DON has been suggested to be indicative of a N deposition gradient, the existence of this relationship for sites that receive similar atmospheric N deposition suggest that the relationship between NO3? and the DOC/DON ratio is derived from environmental and physical factors. Our results suggest that, despite similar wet N deposition at the two watershed sites, N solutes entering lakes were strongly affected by hydrology associated with groundwater contribution and the presence of wetlands, whereas N solutes leaving lakes were strongly influenced by in‐lake processing. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   
30.
选择三亚鹿回头近岸海域常见的鹿角杯形珊瑚(Pocillopora damicornis)幼虫为研究对象,采用室内连续培养的方法,探究了升温(29℃和31℃)与硝酸盐加富(0、5、20μmol/dm^3)对鹿角杯形珊瑚幼虫共生体的生理影响。结果表明:升温和硝酸盐加富对鹿角杯形珊瑚幼虫存活率与共生虫黄藻叶绿素荧光指数(Fv/Fm)无显著影响,但对幼虫附着率的影响表现为明显的交互作用。升温条件下,各处理珊瑚幼虫附着率均显著下降,且硝酸盐加富加剧了升温对珊瑚幼虫附着率的负面影响。再者,升温对幼虫呼吸速率的影响与硝酸盐的浓度有关,5μmol/dm^3硝酸盐处理抵消了升温对幼虫呼吸的促进作用;与此同时,5μmol/dm^3硝酸盐处理提高了幼虫的净光合作用而且光合呼吸速率比(PG/RD)大于2,表明此时珊瑚幼虫共生体系光合作用固定的有机碳为净累积。综上,适量的硝酸盐加富可以缓解升温对珊瑚幼虫代谢的负面影响,但高浓度硝酸盐加富则会不利于鹿角杯形珊瑚幼虫的附着及种群的本地补充。  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号