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排序方式: 共有491条查询结果,搜索用时 15 毫秒
41.
探讨淡水养殖尤其是大水域网箱养鱼中由于投饵方式的不当和投饵量过多导致过剩饵料沉积引起水域环境污染的解决方法。本研究利用鱼类的听觉生物学特性,参考音响驯化技术的有关参数,结合投饵用400 Hz正弦波连续音对鲤(Cyprinus carpioLinnaeus)进行了音响驯化实验。结果表明,最初放声时,实验鱼产生惊愕反应,迅速离声源而去;但驯化6 d后,实验鱼在放声后迅速游向声源,摄食时间由最初的150 s缩短到实验后期的60 s。整个实验阶段放声组与对照组摄食时间差异极显著(P<0.01),摄食率和特定生长率无显著差异(P>0.05)。根据实验鱼的生长参数,求得了参考投饵量曲线和方程。本实验结果为音响驯化技术在淡水鱼养殖中的推广应用提供了基础数据。 相似文献
42.
Macrofauna Communities in the Eastern Mediterranean Deep Sea 总被引:1,自引:0,他引:1
Abstract. During two expeditions with RV ‘Meteor’ in summer 1993 and winter 1997/98 the structural and functional diversity of the benthic system of the highly oligotrophic eastern Mediterranean deep sea was investigated. The macrofauna communities were dominated by polychaetes even at the deepest stations. The fauna at shallow stations was dominated by surface deposit feeders, whereas subsurface deposit feeders and predators generally increased with depth. A high percentage of suspension‐feeding Porifera was found in the Levantine Basin. Mean abundance and number of taxa of both expeditions were significantly correlated to depth and distance to the nearest coast as well as to the total organic carbon (TOC) content in sediments. Numbers of taxa and abundance decreased generally with depth, although lowest numbers were not found at the deepest stations but in the extremely oligotrophic Levantine and Ierapetra Basin. Biomass measured during the second cruise was extremely low in the Ierapetra Basin and comparable to other extreme oligotrophic seas. The significant correlations found for TOC contents and macrofauna with distance to coast during both expeditions apparently reflect the role of hydrographically governed transport of organic matter produced in coastal regions into greater and extreme depths of the Mediterranean Sea. Seasonal differences in macrofauna communities due to seasonal differences in food supply were not found. However, recent large‐scale hydrographic changes (Eastern Mediterranean Transient, EMT) might change the oligotrophy and, thus, the structure of the benthic communities in the Eastern Mediterranean deep sea. 相似文献
43.
Ana C. Silva Ana C. Amador Sónia Brazão Claúdia Faria Diana Boaventura 《Marine Ecology》2010,31(4):525-532
Patellid limpets are key species on rocky shores, structuring intertidal assemblages through their grazing. Their role as prey for fish is, however, often overlooked in studies of intertidal ecosystem functioning. The shanny Lipophrys pholis is a common predator of limpets on rocky shores in Northern Europe and, in this study, we examined the characteristics of its predation on limpets based on prey size. The limpet size range that adult L. pholis (10–12.5 cm) can eat was examined in the laboratory using Patella depressa in 0.2 cm classes, varying between 0.5 cm and 3.0 cm in maximum shell length. There was a limpet size refuge above 1.8 cm, while all smaller sizes were readily consumed by the shanny. The predator attacking behaviour was also examined and found to vary with prey size. Limpets up to 0.8 cm were crushed by the jaw‐constricting force and eaten whole, whereas larger prey were prised from the substratum and the body subsequently separated from the shell. To examine whether there was a L. pholis preference for P. depressa size, a two‐stage laboratory experiment was done using two size classes defined as small (0.7–0.8 cm maximum shell length) and large (1.5–1.6 cm maximum shell length). In the first stage, the predator was given each limpet size class separately. In the second stage, the fish was given a choice between the two classes. Lipophrys pholis was shown to have a preference for the large size class (1.5–1.6 cm). The average number of limpets consumed by the shanny was examined for the duration of one high‐tide typical of the central region of Portugal (≈ 4 h). On average, approximately five limpets (up to an eight limpet maximum) were consumed. The present study shows that L. pholis has a feeding preference based on limpet size, which suggests that the limpet population structure and intra‐ and inter‐specific interactions may be influenced by the shanny predation. 相似文献
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46.
针对动态规划在供水库群优化调度中存在"维数灾",且难以获得真正最优解这一缺点,将改进的加速遗传算法应用到供水库群的水资源优化配置之中。在加速遗传算法中,嵌入局部搜索,以加强算法的全局寻优能力。以库群间的水利联系为线索,设计了相应的算法框架,并提出了供水策略区间的概念。为了体现该算法的优越性,以二个串联供水水库的水资源优化配置为例,选用该方法与基于动态规划的轮库迭代法进行比较研究。结果表明该方法合理可行、收敛速度快,有一定的实用性。 相似文献
47.
提要 在梭子蟹的单体筐养养殖系统中,试验了生态掩体(砂盒)中不同的砂粒粒径大小以及砂层厚度对梭子蟹幼蟹摄食行为与生长特性的影响。砂粒粒径设三个水平,分别为:>2 mm、<0.2 mm以及混合砂;砂层厚度有0cm、2cm、5cm、8cm四个水平。试验共进行6天,结果表明:砂粒粒径及砂层厚度对梭子蟹幼蟹的摄食与生长都有明显的影响。从砂粒粒径看,幼蟹在细砂(SPS)中挖洞休息,蟹体与砂面呈30-45°角,仅露眼睛及触角在外。一天内有3-6次进食,总进食时间为142.7±22.52 min,在摄食次数、总进食时间、平均摄食量(0.2427±0.0137 g/gBW)、以及脱皮及成活率都远高于其他粒径组,该组中幼蟹的体重增长最快,增加了0.814±0.113 g,增长率为91.5±3.43%;而该组的饵料系数(FCR)最低为1.17±0.11。因此,筐养养殖系统砂掩体的砂粒粒径最好为0.2 mm以下。砂层厚度也有类似结果,5 cm以上厚度养殖效果最佳。平均摄食量为0.2087±0.0046 g/gBW,该厚度下,幼蟹无死亡、100%脱皮,体重也增加最快,增加了0.791±0.121 g,增长率为88.9±3.74%,饵料系数(FCR)达到1.37±0.23,表明筐养系统掩体中砂层厚度要在5 cm以上。三种保护性酶类(SOD, POD, CAT)活性随着砂粒粒径变小和砂层厚度增加而降低,而消化酶类(淀粉酶、蛋白酶、脂酶)活性则表现与保护性酶类相反特性。从两类酶的活性变化也能证实,在优选条件下(细砂、厚度>5 cm),幼蟹所受的胁迫在降低。 相似文献
48.
D. J. Edwards 《新西兰海洋与淡水研究杂志》2013,47(2):341-350
In each of eight 5‐day pond experiments carried out at intervals over a year, 0+ to 1 +‐year‐old grass carp, Ctenopharyngodon idella Val., were offered a choice of at least 10 species of water weeds from the Rotorua area. Water temperature was measured each day. Food selectivity decreased with increasing temperature and size of fish, but preference for the weeds did not change. At summer temperatures the fish ate much weed and grew at about 4g/fish/day, but in winter little food was taken and growth was slow. 相似文献
49.
D. J. Staples 《新西兰海洋与淡水研究杂志》2013,47(3):365-374
Growth of the red gurnard, Chelidonichthys kumu (Lesson and Garnot), from Pegasus Bay, Canterbury, was measured during 1966–67. Otoliths were used as an indicator of fish growth; mean length‐at‐age data were obtained from back‐calculated fish lengths at the time of formation of successive annual rings in the otoliths. Growth in length was found to be adequately expressed by the von Bertalanffy growth equation : lt = 52.0 [1 ‐ e‐0.406 (t‐o.291)] (where lt is the fork length in cm at age t). The length: weight relationship was: w = 78.56 × 10‐4 l 3.072 (where w is the weight in grams). From this relationship, growth in weight was described by the equation: wt = 1469 [1 ‐ e‐0.406 (t‐0.291)]3. 相似文献
50.