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101.
根据水稻纹枯病发生与危害程度的调查资料,经与各诱病因素的相关性分析,组建成早、晚稻纹枯病的长期预测模型。经1990~1994年的应用检验,预测准确率达80%以上。  相似文献   
102.
Hybrid sterility is a major hindrance to utilizing the heterosis in indica-japonica hybrids. To isolate a gene Sc conferring the hybrid sterility, the locus was mapped using molecular markers and an F2 population derived from a cross between near isogenic lines. A primary linkage analysis showed that Sc was linked closely with 4 markers on chromosome 3, on which the genetic distance between a marker RG227 and Sc was 0.07 cM. Chromosome walking with a rice TAC genomic library was carried out using RG227 as a starting probe, and a contig of ca. 320 kb covering the Sc locus was constructed. Two TAC clones, M45EI4 and M90J01 that might cover the Sc locus, were partially sequenced. By searching the rice sequence databases with sequences of the TACs and RG227 a japonica rice BAC sequence, OSJNBb0078P24 was identified. By comparing the TAC and BAC sequences, six new PCR-based markers were developed. With these markers the Sc locus was further mapped to a region of 46 kb. The results suggest that the BAC OSJNBb0078P24 and TAC M45EI4 contain the Sc gene. Six ORFs were predicted in the focused 46-kb region.  相似文献   
103.
A Double Haploid (DH) population, 116 plants, derived from the cross between Japonica upland rice IRAT109 and paddy rice Yuefu, planted in PVC pipe under upland ecosystem in 2001 and 2002, was used in this study. Seven root traits, including basal root thickness (BRT), total root number (RN), maximum root length (MRL), root fresh weight (RFW), root dry weight (RDW), ratio of root fresh weight to shoot fresh weight (RFW/SFW) and ratio of root dry weight to shoot dry weight (RDW/SDW), were studied. Using index of drought resistance (IDR), the ratio of yield under upland ecosystem to yield under lowland ecosystem of DH lines, as the criteria of drought resistance, and correla-tion analysis between root traits and IDR, showed that BRT, MRL and RN were significantly correlated with IDR. High IDR lines had thicker BRT, longer MRL and less RN than low IDR lines. A molecular linkage map with 94 RFLP markers and 71 SSR markers covering 1535.1 cM was pro-duced. QTLs and G譋 interactions for BRT, RN, MRL, RFW, RDW, RFW/SFW and RDW/SDW were obtained based on the constructed molecular linkage map and soft-ware QTLmapper version 1.0. A total of 18 additive QTLs and 18 pairs of epistatic QTLs associated with root traits were detected. There were nine additive QTLs and two pairs of epistatic QTLs performed significant interactions with environment. Some QTLs with high general contribution and no G譋 interaction were obtained. Two pairs of epistatic QTLs mrl3 and mrl8, brt3 and brt11a controlling MRL and BRT had high general contributions of 21.51% and 13.03% respectively. An additive QTL and a pair of epistatic QTLs controlling RFW and RDW had high general contributions of 13.50% and 25.64% respectively. Marker assisted selec-tion (MAS) for rice drought resistance based on QTL with high general contribution, low G譋 interaction and tightly linkage with IDR were also discussed.  相似文献   
104.
水稻花培育种技术操作和无性系变异体选择   总被引:3,自引:0,他引:3  
概述了水稻花培育种的技术操作程序和细胞无性系变异的选择方法。选择合适的水稻花培起始材料,选用适宜的培养基配方,对于水稻花培中愈伤组织诱导和分化至关重要。某些增效因子(例如水解乳蛋白、单核苷酸、AgNO3等)可提高灿稻花培的绿苗分化率。无性系变异为农作物细胞工程育种提供丰富的选择材料。通过对细胞变异的研究,建立了裸米选择-测米培胚的技术方法,并选育出多个高蛋白量的水稻优质品种(品系)。  相似文献   
105.
106.
以温敏核不育系810S为对照,对810S的淡黄叶突变体标810S叶绿素含量、净光合速率、暗呼吸速率和生物产量进行了比较研究.结果表明:淡黄叶突变体标810S各叶位叶绿素含量均比对照810S低,其光合色素含量的变化幅度为对照的60.9%~50.4%,但标810S各叶位净光合速率比对照高,增加幅度为4~5μmol.m-2.s-1.各发育时期的暗呼吸速率标810S比对照高0.23~0.35μmol.m-2.s-1,株高和生物学产量与810S接近.  相似文献   
107.
微波辅助提取米糠多糖的工艺   总被引:3,自引:0,他引:3  
以脱脂挤压米糠为原料,采用微波辅助法提取米糠多糖,并与传统热水浸提方法进行比较,通过考察料液比、微波辐射时间以及微波功率三个因素,设计正交试验,得出微波辅助提取米糠多糖的优化工艺条件为:料液比1:10,微波辐射时间为2min,微波炉功率400W.传统热水浸提米糠多糖提取率为2.02%,纯度为68.53%,微波辅助提取多糖的提取率为2.76%,纯度为72.47%.与传统热水浸提方法相比较,微波辅助法的米糠多糖提取率和纯度分别提高了36.6%和5.7%.微波辅助法提取可以显著提高米糠多糖的提取效率,但对其理化性质并无影响.  相似文献   
108.
109.
一个水稻抗纹枯病突变体的遗传分析及其基因的初步定位   总被引:3,自引:0,他引:3  
高水平抗纹枯病突变体和高感纹枯病品种蜀恢881杂交构建分离群体,经F2分离世代的遗传分析,抗、感单株比例符合3 1(χc2=0.563,χ12,0.05=3.84),初步确定该突变体对纹枯病的抗性由一对显性主效基因所控制,命名为Rsb-2(t)。利用已合成的530对微卫星引物,对抗纹枯病突变体和蜀恢881进行多态性引物筛选,用多态性引物对上述F2分离群体的全部感病单株和部分抗病单株的DNA进行PCR分析,借助MAPERMAKER/EXP3.0软件,对其微卫星标记实验数据进行连锁分析,将Rsb-2(t)定位于第3染色体的p臂,发现RM218、RM251、RM4321和RM5748与Rsb-2(t)连锁,它们均位于着丝粒端,连锁距离分别为32.1 cM,41.1 cM,42.4 cM和49.7 cM。研究结果为进一步对该基因的精细定位奠定了基础。  相似文献   
110.
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