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31.
应力释放模型的改进及其在研究台湾地区地震预测问题中的应用. 总被引:2,自引:0,他引:2
应力释放模型过去主要用于研究大范围历史大地震活动规律.本文对应力释放模型进行了改进,对其能否运用于区域更小、时段更短、震级更低的情况进行了探讨;以台湾地区近百年6级以上地震为例的研究结果表明,应力释放模型仍然适用.在回溯性的地震预测检验中,用改进的应力释放模型计算出台湾地区地震发生的条件概率强度,并用其预测6级以上地震的发震时刻.结果表明,其预测精度优于泊松模型. 相似文献
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Byron C. Shumate Claire L. Schelske Thomas L. Crisman William F. Kenney 《Journal of Paleolimnology》2002,27(1):71-77
A paleolimnological evaluation of cladoceran microfossils was initiated to study limnological changes in Lake Apopka, a large (125 km2), shallow (mean depth = 1.6 m), warm, polymictic lake in central Florida. The lake switched from macrophyte to algal dominance in the late 1940s, creating a Sediment Discontinuity Layer (SDL) that can be visually used to separate sediments derived from macrophytes and phytoplankton. Cladoceran microfossils were enumerated as a means of corroborating extant eutrophication data from the sediment record. Inferences about the timing and trajectory of eutrophication were made using the cladoceran-based paleo-reconstruction. The cladoceran community of Lake Apopka began to change abruptly in both total abundance and relative percent abundance just before the lake shifted from macrophyte to algal dominance. Alona affinis, a mud-vegetation associated cladoceran, disappeared before the SDL was formed. Planktonic and benthic species also began to increase below the SDL, indicating an increase in production of both planktonic and benthic species. Chydorus cf. sphaericus, an indicator of nutrient loading, increased relative to all other cladocerans beginning in the layer below the SDL and continuing upcore. Changes in the transitional sediment layer formed before the lake switched to phytoplankton dominance, including an increase in total phosphorus concentration, suggest a more gradual eutrophication process than previously reported. Data from this study supported conclusions from other paleolimnological studies that suggested anthropogenic phosphorus loading was the key factor in the hypereutrophication of Lake Apopka. 相似文献
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Pore‐ice sublimation is a prerequisite for aeolian activity in cold environments where surface sediments hold significant amounts of frozen water. Few quantitative studies have defined the rate of grain release from cemented surfaces by pore‐ice sublimation. In 1996–1997, controlled field experiments at Presqu'ile Beach, Ontario, were implemented to measure sediment release from frozen surfaces. The release rates were compared to the local wind regime, ambient temperature and humidity. In additional field experiments, the effect of sediment water content on grain release by sublimation was examined. From the experimental results, an equation which predicts grain release based on local wind speed, ground temperature, humidity, and surface water content is proposed. Predicted release rates show reasonable agreement with natural deflation measured on the beach at Presqu'ile Provincial Park. 相似文献
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根据国内提出的控制饮用水生物稳定性的可同化有机碳(AOC)标准,通过配制水样研究了AOC及细菌再生长潜力(BRP)同水中磷含量的关系;同时针对净水工艺试验出水水样,考察了水中的磷同其生物稳定性的关系。结果表明,对于配水水样,在一定的磷浓度范围内,磷是水中细菌生长的限制因子;在净水试验工艺出水水样中添加50μg/L的PO43--P后,AOC增加了55%,BRP增加了123%,表明水中磷是其生物稳定性的限制因子。由于常规的净水工艺对水中的磷可以有效去除,把水中总磷(TP)控制在5μg/L内来提高饮用水生物稳定性具有一定的可能性和现实性。 相似文献
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滇池微生物解磷与聚磷作用的实验研究及磷的现代沉积与微生物成矿作用 总被引:4,自引:0,他引:4
滇池是世界上磷质来源最丰富的湖泊,是研究磷的现代沉积和微生物对磷循环作用及微生物成矿的天然场所。研究发现,滇池微生物种群和数量繁多,但能对磷溶解、转化、迁移、聚集、沉积的微生物主要有解磷菌和聚磷菌两类。这两类微生物与滇池磷的含量之间有一系列规律的相关性:在底泥磷高含量区域,解磷菌的种群和数量与底泥磷含量成负相关关系,与水体磷含量成正相关关系,而聚磷菌的种群和数量与底泥磷含量成正相关关系,与水体磷含量成负相关关系;在底泥磷低含量区域,上述相关性则相反。滇池中这种活着的微生物在自然环境条件下对磷的溶解、转化、迁移、聚集和沉积的作用,对古磷块岩微生物成矿说提供了可靠的依据,而且对以磷为限制性因子的湖、海、江河环境污染的防治提供了理论资料。 相似文献
38.
Sediment Phosphorus Chemistry and Microbial Biomass along a Lowland New Zealand Stream 总被引:1,自引:0,他引:1
R. W. McDowell 《Aquatic Geochemistry》2003,9(1):19-40
An evaluation of the distribution of P concentrations in streamflow, P fractions andthe microbial biomass P pool was made of bed and bank sediments along a lowlandstream in New Zealand. Agricultural intensification increased downstream. However,most P fractions decreased downstream (total P decreased from c. 400 to 250 mg kg-1) in bed sediments, while P in streamflow remained relatively constant (generally < 0.005 mg l-1) and sediment microbial P increased from 2 to 8 mg kg-1. An investigation of P release from dried and rewetted sediments showed that solution P (CaCl2-P) increased, on average > 300%, and proportional to the size of the microbial biomass P pool before drying, except in sediments with much organic carbon (OC). When supplied with a P source (1 mg l-1) and then simultaneously with a C source (glucose, 100 mg l-1), all sediment behaved similarly and biotic sorption accounted for, on average, 27 and 34% of the total sediment uptake, respectively (maximum of 58%). The quantity of P taken up was related to the initial size of the microbial biomass P pool, and the availability of P as influenced by organic P complexes and OC. The sediment microbial biomass represents a transient, but small store of P could be useful to indicate bioavailable P inputs. 相似文献
39.
R. Hellmann J.-M. Penisson R. L. Hervig J.-H. Thomassin M.-F. Abrioux 《Physics and Chemistry of Minerals》2003,30(4):192-197
Using an approach combining high-resolution and energy-filtered transmission electron microscopy (HRTEM and EFTEM), we have studied with Å to nm-spatial resolution the interfacial region that delimits the near-surface altered zone and non-altered labradorite feldspar after dissolution under acid pH conditions. The interface is characterized by extremely sharp and spatially coincident changes in structure and chemistry. The 500-nm-thick altered zone is depleted in interstitial cations (Ca, Na, K) and Al, a framework element, whereas it is enriched in H, O, and Si. Modeling H+-alkali interdiffusion within a 500-nm-thick altered zone shows that volume interdiffusion cannot reproduce the sharp chemical interfaces measured by EFTEM. Based on these new data, we propose that the near-surface altered zone is a result of interfacial dissolution-reprecipitation, and not of preferential leaching of cations and interdiffusion with H+. This implies an intrinsic dissolution process that is stoichiometric, where the breaking of bonds and release of interstitial cations and framework elements (Al, Si, and O) to solution occur contemporaneously at equal relative rates from the original fluid–mineral interface. 相似文献
40.