全文获取类型
收费全文 | 138篇 |
免费 | 2篇 |
国内免费 | 5篇 |
专业分类
林业 | 11篇 |
农学 | 9篇 |
基础科学 | 1篇 |
6篇 | |
综合类 | 73篇 |
农作物 | 4篇 |
水产渔业 | 1篇 |
畜牧兽医 | 5篇 |
园艺 | 33篇 |
植物保护 | 2篇 |
出版年
2023年 | 1篇 |
2021年 | 4篇 |
2020年 | 3篇 |
2019年 | 2篇 |
2018年 | 3篇 |
2017年 | 6篇 |
2016年 | 8篇 |
2015年 | 4篇 |
2014年 | 8篇 |
2013年 | 8篇 |
2012年 | 12篇 |
2011年 | 17篇 |
2010年 | 12篇 |
2009年 | 13篇 |
2008年 | 9篇 |
2007年 | 11篇 |
2006年 | 8篇 |
2005年 | 3篇 |
2004年 | 1篇 |
2003年 | 5篇 |
1996年 | 1篇 |
1995年 | 2篇 |
1994年 | 1篇 |
1993年 | 2篇 |
1992年 | 1篇 |
排序方式: 共有145条查询结果,搜索用时 31 毫秒
1.
2.
During 2012–2014 surveys for the presence of phytoplasma diseases in Fars province (Iran), pomegranate little leaf symptoms were observed in several orchards in Khafr and Neyriz areas. Samples collected from symptomatic plants positively reacted in nested PCR assays using P1/P7 followed by R16F2n/R16R2 primer pairs producing the expected 1,250 bp DNA fragments. Real and virtual RFLP analysis showed that the sequences of phytoplasma strains from Khafr and Neyriz (KPLL and NPLL strains, respectively) were identical to each other and belong to 16SrII phytoplasma group, subgroup D. Phylogenetic analysis of the R16F2n⁄R16R2 DNA region confirmed that KPLL and NPLL phytoplasmas were enclosed in the same clade as other 16SrII-D subgroup phytoplasmas. This is the first reported occurrence of a 16SrII phytoplasma infecting pomegranate trees. 相似文献
3.
Pomegranate fruit is an important source of potentially healthy bioactive compounds and mineral nutrients. Changes in total phenolic compound, concentrations, and levels of macronutrients (P, K, N, Mg, Ca and Na) and micronutrients (Zn, Cu, Mn, Fe and B) in arils and peel of pomegranate fruit were recorded from 10 days after full bloom until harvest. Total phenolics levels increased at early stage of growth both in peel and arils of fruit, but thereafter generally decreased during maturation and reached to 3.70 and 50.22 mg g−1 of dry weight in arils and peel, respectively, at harvest. The amount of total phenolics in peel was markedly higher than arils of pomegranate fruit. The concentration of most elements in arils and peel decreased during fruit growth and development. At harvest the relative order of concentration of macronutrients both in arils and peel was K > N > Ca > P > Mg > Na. The concentration of most micronutrients was greater in the arils than in the peel especially in early season. The relative order of concentration of micronutrients in arils was B > Fe > Zn > Cu > Mn. The accumulation of all the macro- and microelement within the fruit also increased during fruit growth and development. These results provide important data on total phenolics and macro- and micronutrient changes during fruit growth and development, emphasizing that pomegranate fruit can be a good source of bioactive compounds and minerals. 相似文献
4.
5.
石榴DNA提取方法的比较及抗氧化剂对DNA质量的影响* 总被引:8,自引:1,他引:8
比较了SDS-CTAB微量提取法和改进的SDS微量提取法提取的石榴叶片DNA质量,结果认为两种方法提取的DNA均可用于RAPD分析,但SDS微量提取法较适合于石榴叶片DNA的提取。试验中还研究了抗氧化剂PVP,α-巯基乙醇和抗坏血酸3种试剂单独使用及PVP与α-巯基乙醇混合使用对SDS-CTAB微量提取法的影响,发现与对照相比,单独加抗坏血酸及PVP与α-巯基乙醇混合使用能很好地防止DNA在提取过程中的褐化。 相似文献
6.
7.
8.
在蛋仔公鸡饮水中添加石榴皮煎提剂后,石榴果皮煎剂能够显著提高免疫器官指数和单核吞噬细胞吞噬指数,并且以1%的添加水平效果最好。 相似文献
9.
[目的]测定并分析比较不同花期石榴花蜂蜜中黄酮类化合物含量。[方法]用丙酮作萃取剂,以芦丁为标准对照品,采用分光光度法测定了2011和2012年云南蒙自石榴花期采集的24个蜂蜜样品的总黄酮含量,并对各年不同生产批次蜂蜜黄酮含量进行比较。[结果]试验得出,2011年石榴花蜂蜜黄酮平均含量(23.60±1.36)mg/kg,显著高于2012年平均含量(17.10±0.53)mg/kg。同时得出,石榴不同花期生产的蜂蜜中黄酮含量不同,随花期变化而改变,盛花期高于初花期和末花期,初花期到盛花期含量升高,盛花期到末花期含量降低。[结论]研究可为石榴花蜂蜜的开发利用以及功能研究提供参考依据。 相似文献
10.
Sequential subculturing leads to a gradual physiological change in cells that may be termed ‘rejuvenation’. The effect of repetitive subculturing on callus induction and shoot regeneration from leaf explants of Punica granatum L. ‘Kandhari Kabuli’ were investigated. Surface-sterilised leaves were cultured on 1.0× Murashige and Skoog (MS) medium supplemented with 4.0 mg l–1 α-naphthaleneacetic acid (NAA) and 2.0 mg l–1 6-benzyladenine (BA) for callus induction. Shoots were regenerated from callus on 1.0× MS medium supplemented with 1.5 mg l–1 BA, 0.5 mg l–1 kinetin, and 0.25 mg l–1 NAA. Subculturing of callus onto fresh medium maintained the rate of shoot formation and substantially increased the production of shoot buds up to the second subculture. Following further subculture passages, a lower shoot regeneration potential from callus was observed. A maximum shoot bud induction from callus of 63.9% was observed at the second subculture passage. The rate of multiplication of in vitro shoots increased until the fourth subculture, then became constant. Similarly, in vitro rooting of micro-shoots increased up to the third subculture, followed by a decline during further subculturing. 相似文献