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51.
R.Afza  H.Brunner 《核农学报》1996,10(4):216-220
<正> The number of somatic embryos and regenerated plantlets were directly induced from irra-diated rice roots of the variety Taipei 309(Oryza sativa L.).For the induction of somatic em-bryos,the suitable age of roots was no more than 7 days after seed culture on the medium and thesections near tip were more vigorous than those near base of a root;the number of somatic em-bryos induced by the media with 1.11mg/L2,4-D plus 0.47mg/L NAA and 2.21mg/L 2,4-Dplus 1.86mg/L NAA was much higher than that induced by 1.11mg/L 2,4-D alone;10~20 Gyand 40 Gy of γ irradiation were the most favourable for increasing somatic embryo number onthe media of 2.21mg/L 2,4-D plus 1.86mg/L NAA and 1.11mg/L 2,4-D plus 0.47mg/L NAAor 1.11mg/L 2,4-D alone respectively.The highest number of regenerated plantlets was fromthat cultured on the medium of 1.11mg/L 2,4-D plus 0.47mg/L NAA and irradiated with 30~40 Gy of γ rays.  相似文献   
52.
It is well established that increasing soil bulk density (SBD) above some threshold value reduces plant root growth and thus may reduce water and nutrient acquisition. However, formation and elongation of maize seminal roots and first order lateral (FOL) roots in various soil layers under the influence of SBD has not been documented. Two studies were conducted on a loamy sand soil at SBD ranging from 1.25 g cm–3 to 1.66 g cm–3. Rhizotrons with a soil layer 7 mm thick were used and pre‐germinated plants were grown for 15 days. Over the range of SBD tested, the shoot growth was not influenced whereas total root length was reduced by 30 % with increasing SBD. Absolute growth rate of seminal roots was highest in the top soil layer and decreased with increasing distance from the surface. Increasing SBD amplified this effect by 20 % and 50 % for the top soil layer and lower soil layers, respectively. At the end of the experiment, total seminal roots attributed to approximately 15 % of the total plant root length. Increasing SBD reduced seminal root growth in the lowest soil layer only, whereas FOL root length decreased with SBD in all but the uppermost soil layer. For FOL, there was a positive interaction of SBD with distance from the soil surface. Both, increasing SBD and soil depth reduced root length by a reduction of number of FOL roots formed while the length of individual FOL roots was not influenced. Hence, increasing SBD may reduce spatial access to nutrients and water by (i) reducing seminal root development in deeper soil layers, aggravated by (ii) the reduction of the number of FOL roots that originate from these seminal roots.  相似文献   
53.
伐后竹蔸清理技术研究   总被引:2,自引:0,他引:2  
分析了现有竹林伐后竹蔸(桩根)清理技术的缺点,即人工挖掘劳动强度较大,劈裂腐烂法其林地更新速度较慢,化学腐蚀法的剩余化学试剂会对大气环境造成一定污染等,设计了一种质量轻、体积小、移动方便、功效高,且能在地形土质复杂的稠密竹林内移动作业的竹蔸清理设备.  相似文献   
54.
Soil compaction is one of the major problems facing modern agriculture. Overuse of machinery, intensive cropping, short crop rotations, intensive grazing and inappropriate soil management leads to compaction. Soil compaction occurs in a wide range of soils and climates. It is exacerbated by low soil organic matter content and use of tillage or grazing at high soil moisture content. Soil compaction increases soil strength and decreases soil physical fertility through decreasing storage and supply of water and nutrients, which leads to additional fertiliser requirement and increasing production cost. A detrimental sequence then occurs of reduced plant growth leading to lower inputs of fresh organic matter to the soil, reduced nutrient recycling and mineralisation, reduced activities of micro-organisms, and increased wear and tear on cultivation machinery. This paper reviews the work related to soil compaction, concentrating on research that has been published in the last 15 years. We discuss the nature and causes of soil compaction and the possible solutions suggested in the literature. Several approaches have been suggested to address the soil compaction problem, which should be applied according to the soil, environment and farming system.

The following practical techniques have emerged on how to avoid, delay or prevent soil compaction: (a) reducing pressure on soil either by decreasing axle load and/or increasing the contact area of wheels with the soil; (b) working soil and allowing grazing at optimal soil moisture; (c) reducing the number of passes by farm machinery and the intensity and frequency of grazing; (d) confining traffic to certain areas of the field (controlled traffic); (e) increasing soil organic matter through retention of crop and pasture residues; (f) removing soil compaction by deep ripping in the presence of an aggregating agent; (g) crop rotations that include plants with deep, strong taproots; (h) maintenance of an appropriate base saturation ratio and complete nutrition to meet crop requirements to help the soil/crop system to resist harmful external stresses.  相似文献   

55.
首先对不锈钢材料的切削性能和不锈钢材料的攻丝特点进行分析,介绍了振动攻丝的基本原理,利用自行设计的振动攻丝机进行振动攻丝与传统机械攻丝和手动攻丝的对比实验分析,结果表明振动攻丝具有降低攻丝扭矩、提高牙形精度和螺距精度的效果.最后通过对振动攻丝的攻丝现象进行分析,利用振动攻丝弹塑性再切削和丝锥刚性化效果解释高强度材料攻丝过程的本质是降低攻丝扭矩,提高攻丝质量.  相似文献   
56.
丝瓜子叶原生质体培养研究   总被引:3,自引:0,他引:3  
经1%纤维素酶、0.5%离析酶、3mmol/L MES 和0.25mol/L 甘露醇的CPW 酶液酶离出的丝瓜子叶原生质体,在去NH_4NO_3的KM_(8p)附加0.5mg/L 2、4-D、lmg/L BA、125mg/L 水解酪蛋白(CH)、0.15~0.20mol/L 葡萄糖和0.05mol/L 蔗糖的培养基上培养出微愈伤组织,再经MS附加多种成分的培养基培育,增殖出大量松散粒状、表面光滑的多种形态愈伤组织,并分化出根。  相似文献   
57.
为进一步了解木本植物不定根发生、发育的机理,对苹果砧木M26试管苗不定根的发生、发育过程进行解剖观察,利用十二烷基磺酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)对M26试管苗在接入生根培养基前后,不同时期表达的蛋白进行了研究。结果发现:在不定根原基形成和发育的阶段性过程中,茎基部蛋白质的种类和数量出现明显差异。生根培养后,在继代苗茎基部表达的5条蛋白条带减弱或消失,其分子量分别为26.8 kDa、37kDa、40.3 kDa、43 kDa和66 kDa;明显表达了4条新的蛋白条带,其分子量分别为26 kDa、27.7 kDa、32.5 kDa、和45 kDa,同时有4条蛋白条带(38.5 kDa、42 kDa、53.2 kDa和55.5 kDa)其表达丰度提高。多种蛋白条带的消失和出现,可作为M26试管苗不定根产生的生化标志。在不定根原基逐步形成发育的同时,有3条蛋白条带的表达丰度也逐步提高,可作为不定根形成过程表达的特异标记蛋白带。  相似文献   
58.
红锥切根育苗试验研究   总被引:8,自引:0,他引:8  
通过红锥切根、沾灰育苗试验,分析成苗率、苗高、地径、主根、须根及枝、叶等一系列苗木数量、质量性状的差异。结果表明:切根能使红锥苗木主根变短,侧根部位提高,根系发达,苗木地径和苗高明显增加,生长旺盛。但切根也在一定程度上降低了成苗率。  相似文献   
59.
提取高质量茶树总RNA的方法研究   总被引:7,自引:2,他引:7  
由于茶树富含多糖、多酚,从茶苗组织中尤其是从茶苗的根中提取高质量的RNA较为困难,试用了多种方法都未能获得高质量的RNA.为此,作者借鉴多年生的草本植物RNA提取方法-CTAB法,并在此基础上进行了改进,首次提取茶苗嫩根中的总RNA.电泳检测显示,该方法提取的总RNA 28S和18S条带清晰且28S较18S条带亮,紫外光谱分析显示A260/A280的比值为1.93.用于RT-PCR反应,成功克隆了492 bp的谷氨酰胺合成酶基因片段.说明用该方法提取的RNA纯度和完整性好.试用该方法从营养成分丰富的茶籽胚中提取总RNA,效果同样很好.  相似文献   
60.
科尔沁沙地低缓沙丘主要植被根系层土壤水分特性分析   总被引:4,自引:0,他引:4  
土壤与植物是SPAC系统的两个主要要素,本文通过对科尔沁沙地低缓固定沙丘主要植被榆树、小叶锦鸡儿根系发育区域内的土壤水分的取样调查,分析了植被周边土壤水分与植物地上生长形态以及地下根系分布间的关系,并分析了沙地土壤水分的空间分布格局及其主要影响因素。  相似文献   
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