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991.
Genetic diversity in apricot, Prunus armeniaca, aimed at improving resistance to plum pox virus 总被引:2,自引:0,他引:2
Plum Pox Virus, a non-persistent virus transmitted by aphids, causes serious damage to stone fruits. The apricot tree is very sensitive and in order to breed apricot cultivars resistant to Plum Pox Virus and establish breeding strategies, genetic diversity based on 10 enzymatic systems, six of which were polymorphic, has been studied. The plant material studied, 94 accessions, included the most important apricot cultivars grown in PPV-affected areas. Genetic diversity is high and showed important differences between the three geographical groups studied (North African, European and North American). The North American group was very diverse and allozymes can be used to identify three subgroups. Some North American PPV-resistant cultivars were very distant from the rest of the cultivars, mainly due to the presence of rare alleles found in an Asian apricot related species. These results support the hypothesis that Asian-related species might be the origin of PPV resistance within the North American cultivars. Three North American cultivars have been considered as putative donors of PPV resistance to the European cultivars because of their agronomic behaviour, chilling requirements and distance from European cultivars. However, to increase the genetic variability of the European group and thereby to favour recombination, the study of Asian apricot resources is also recommended. 相似文献
992.
Stylar ribonucleases in almond: correlation with and prediction of incompatibility genotypes 总被引:5,自引:0,他引:5
R. Bskovic K. R. Tobutt I. Batlle H. Duval P. Martinez-Gomez T. M. Gradziel 《Plant Breeding》2003,122(1):70-76
To clarify incompatibility relationships among almond cultivars, 35 were analysed for stylar ribonucleases, which have previously been shown to correlate with incompatibility S alleles. Stylar proteins were extracted and separated electrophoretically and the zymograms compared with ladders of ribonucleases corresponding to the 12 S alleles previously reported. Sixteen cultivars showed a band corresponding to two of the known ribonucleases, 17 showed one known ribonuclease and one ‘new’ band, and two showed two new bands. Twelve new ribonucleases were detected; 11 were attributed to new S alleles (S13 to S23) and a mutant form of S7 was attributed to S7A. Genotypes were proposed for nine cultivars of five incompatibility groups that had not been genotyped previously, VII, X, XI, XII and XIII. Twenty‐four cultivars of unknown incompatibility relationships were provisionally genotyped: six of these could be assigned to existing groups and two new groups were established, XIV and XV, along with group O of cultivars with unique genotypes. Test crosses confirmed that eight pairs of cultivars showing similar zymograms were indeed cross‐incompatible, including the two representatives of each of the two new groups. Virtually all self‐incompatible cultivars of known genotype are listed in a table. The data should be useful for planning cultivar combinations for orchards and for designing crosses for breeding programmes. 相似文献
993.
Haploids in apple were induced using anther culture and in situ parthenogenesis followed by in vitro culture of immature embryos or cotyledons. In addition to an earlier characterization of the zygosity state using isozymes, the purpose of this work was an analysis of simple sequence repeats (SSRs) to describe the homozygosity more comprehensively. Five previously described SSR primer combinations were applied. Initially, polymerase chain reaction amplification with the primer pairs was performed on the donor genotypes ‘Alkmene’ and ‘Remo’ and on a further four apple cultivars. Only those primer pairs that amplified two different contrasting alleles could be used for investigation of the zygosity state. According to these analyses both the androgenic and parthenogenic regenerated shoots are homozygous. 相似文献
994.
梅花品种"美人"叶片离体再生体系建立 总被引:1,自引:0,他引:1
以“美人’梅离体培养的叶片为材料进行愈伤组织诱导再生研究,诱导过程分两步,第一步是愈伤组织的诱导,诱导过程中生长素2,4-D起了决定性的作用,并且以液体培养基为佳,而且暗培养的愈伤组织再分化率明显高于光培养。具体培养基为1/2WPM+5mg/L 2,4-D;第二步是在愈伤组织诱导出之后,进一步诱导愈伤组织再生出植物,在经过7d液体培养基的诱导之后将离体叶片转入1/2WPM+1.0mg/L 6-BA+0.1mg/L NAA+8mg/L AgNO3+100mg/L水解乳蛋白培养,再分化率可以达到24.25%。愈伤组织分化出苗之后,进一步诱导生根,“美人”梅最佳生根培养基是1/2WPM+0.5mg/L NAA。 相似文献
995.
996.
He Tian-Ming Chen Xue-Sen Xu Zheng Gao Jiang-Sheng Lin Pei-Jun Liu Wen Liang Qing Wu Yan 《Genetic Resources and Crop Evolution》2007,54(3):563-572
Genetic structure of three wild populations (Xinyuan, Gongliu and Daxigou) of apricot in the Ily Valley, Xinjiang Uygur Autonomous
Region of China, was investigated with microsatellite (simple sequence repeat, SSR) markers. The higher polymorphism and greater
transportability of these markers between Prunus species proved SSR markers were much efficient for conducting genetic diversity studies in wild apricot. Nei's gene diversity
(He) and Shannon's index of diversity (I) were 0.287 and 0.458, respectively. This indicated that the wild apricot in the Ily Valley still maintained a relatively
high level of diversity. The Gst of 0.137 and Fst of 0.164 revealed that genetic variation mainly resided among individuals
within populations (83.6–86.3%). Population differentiation could also be found according to the distribution of SSR alleles
between the populations. Mantel test showed the genetic distance between populations was significantly correlated to the geographical
distance. The modest amount of gene flow (2.684) would reduce the disjunction between wild apricots. The long-distance dispersal
of pollen by insects was probably the main way of gene flow between populations. Based on the study of population genetic
structure, an effective conservation strategy of the species was discussed. 相似文献
997.
Ten cpSCAR markers that show polymorphism in Prunus avium were used to fingerprint sweet cherry cultivars. The purpose of the study was also to contribute to identification and to
help determine their genetic interrelationships. Samples of ‘0900 Ziraat’, a superior Turkish variety, which were collected
in several locations all over Turkey, had identical cpSCAR patterns, and they resembled a common European haplotype, A. ‘Sweetheart’,
‘Summit’ and ‘Canada Giant’ and their haplotype are intermediate between the previously described haplotypes A and B, which
were originally found in Central and Eastern European sweet and wild cherries, and those from Northern Turkey, respectively.
The data therefore suggests a local maternal descent (within Europe and Asia Minor) of the cultivars analysed. Our results
show that chloroplast DNA analysis is a straightforward way to classify cherry cultivars. We compare our results to others
previously reported for sweet cherry cultivars, and conclude that cpSCAR diversity data could be considered for phylogenetic
studies in this group. 相似文献
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