全文获取类型
收费全文 | 1368篇 |
免费 | 179篇 |
国内免费 | 80篇 |
出版年
2023年 | 37篇 |
2022年 | 29篇 |
2021年 | 50篇 |
2020年 | 59篇 |
2019年 | 59篇 |
2018年 | 58篇 |
2017年 | 52篇 |
2016年 | 70篇 |
2015年 | 64篇 |
2014年 | 62篇 |
2013年 | 74篇 |
2012年 | 62篇 |
2011年 | 62篇 |
2010年 | 48篇 |
2009年 | 70篇 |
2008年 | 70篇 |
2007年 | 67篇 |
2006年 | 60篇 |
2005年 | 54篇 |
2004年 | 50篇 |
2003年 | 45篇 |
2002年 | 45篇 |
2001年 | 34篇 |
2000年 | 45篇 |
1999年 | 34篇 |
1998年 | 38篇 |
1997年 | 32篇 |
1996年 | 28篇 |
1995年 | 20篇 |
1994年 | 18篇 |
1993年 | 15篇 |
1992年 | 15篇 |
1991年 | 15篇 |
1990年 | 11篇 |
1989年 | 11篇 |
1988年 | 9篇 |
1987年 | 10篇 |
1986年 | 10篇 |
1985年 | 6篇 |
1984年 | 7篇 |
1983年 | 3篇 |
1982年 | 3篇 |
1981年 | 3篇 |
1980年 | 2篇 |
1978年 | 4篇 |
1977年 | 1篇 |
1976年 | 1篇 |
1974年 | 1篇 |
1973年 | 1篇 |
1972年 | 1篇 |
排序方式: 共有1627条查询结果,搜索用时 15 毫秒
41.
为系统掌握常春二乔玉兰春夏季开花物候节律,探讨其与营养物质的关系,本研究以6年生常春二乔玉兰为试验材料,观测其年生长发育节律、春夏季开花物候特性以及茎段营养物质的含量变化。结果表明:(1)每年12月始至翌年2月下旬为常春二乔玉兰休眠期。2月下旬花芽膨大生长,并于3月开始春季开花,花期持续约20 d。4月进行营养生长,5月完成花芽分化。5月底部分花芽膨大并于6月开始开花,夏季花期持续约20 d。7~9月为未膨大花芽的发育滞缓期。此外,少量夏季开放的花的基部侧芽再次分化形成花芽。10~12月随着落叶的开始,树体逐渐进入休眠期。(2)常春二乔玉兰营养生长后分化的花芽能够花开两季。春季开花为先花后叶,开花率为100%,开花同步率较高,雌、雄蕊发育正常,为可育花。夏季开花为花叶同放,开花率约为30%,且开花同步率较低,开放的花内雌、雄蕊发育异常,为不育花。(3)春季开花期间可溶性糖和可溶性蛋白呈下降趋势,淀粉含量于开花后期下降;夏季开花期间可溶性糖和淀粉总体呈先降后升趋势,而可溶性蛋白总体呈下降趋势。综上所述,常春二乔玉兰春、夏季开花期内开花模式存在一定差异,其显著节律特征与营养物质含量变化有关,推测低水平的可溶性糖及高水平的淀粉和可溶性蛋白有利于春季开花的启动,而低水平的可溶性蛋白及高水平的可溶性糖和淀粉含量则有利于夏季开花的实现。 相似文献
42.
Colin Bonner Nina A. Sokolov Sally Erin Westover Michelle Ho Arthur E. Weis 《Ecology and evolution》2019,9(7):3770-3783
Gene flow between populations can allow the spread of beneficial alleles and genetic diversity between populations, with importance to conservation, invasion biology, and agriculture. Levels of gene flow between populations vary not only with distance, but also with divergence in reproductive phenology. Since phenology is often locally adapted, arriving migrants may be reproductively out of synch with residents, which can depress realized gene flow. In flowering plants, the potential impact of phenological divergence on hybridization between populations can be predicted from overlap in flowering schedules—the daily count of flowers capable of pollen exchange—between a resident and migrant population. The accuracy of this prospective hybridization estimate, based on parental phenotypes, rests upon the assumptions of unbiased pollen transfer between resident and migrant active flowers. We tested the impact of phenological divergence on resident–migrant mating frequencies in experiments that mimicked a single large gene flow event. We first prospectively estimated mating frequencies two lines of Brassica rapaselected or early and late flowering. We then estimated realized mating frequencies retrospectively through progeny testing. The two estimates strongly agreed in a greenhouse experiment, where procedures ensured saturating, unbiased pollination. Under natural pollination in the field, the rate of resident–migrant mating, was lower than estimated by phenological divergence alone, although prospective and retrospective estimates were correlated. In both experiments, differences between residents and migrants in flowering schedule shape led to asymmetric hybridization. Results suggest that a prospective estimate of hybridization based on mating schedules can be a useful, although imperfect, tool for evaluating potential gene flow. They also illustrate the impact of mating phenology on the magnitude and symmetry of reproductive isolation. 相似文献
43.
Reproductive timing is a key life‐history trait that impacts the pool of available mates, the environment experienced during flowering, and the expression of other traits through genetic covariation. Selection on phenology, and its consequences on other life‐history traits, has considerable implications in the context of ongoing climate change and shifting growing seasons. To test this, we grew field‐collected seed from the wildflower Mimulus guttatus in a greenhouse to assess the standing genetic variation for flowering time and covariation with other traits. We then created full‐sib families through phenological assortative mating and grew offspring in three photoperiod treatments representing seasonal variation in daylength. We find substantial quantitative genetic variation for the onset of flowering time, which covaried with vegetative traits. The assortatively‐mated offspring varied in their critical photoperiod by over two hours, so that families differed in their probability of flowering across treatments Allocation to flowering and vegetative growth changed across the daylength treatments, with consistent direction and magnitude of covariation among flowering time and other traits. Our results suggest that future studies of flowering time evolution should consider the joint evolution of correlated traits and shifting seasonal selection to understand how environmental variation influences life histories. 相似文献
44.
为评价4种种子处理剂对菜心种子的安全性以及对黄曲条跳甲Phyllotreta striolata (Fabricius)的防治效果和保苗作用,本研究开展了室内、田间安全性试验以及田间保护试验。室内安全性试验结果显示,40%溴酰·噻虫嗪种子处理悬浮剂、600 g/L吡虫啉悬浮种衣剂、18%噻虫胺种子处理悬浮剂、54%吡虫·氟虫腈悬浮种衣剂用量分别低于5 120、9 600、2 880、7 040 g(a.i.)/100 kg种子时,对菜心种子发芽和生长无影响。田间安全性及保护作用结果显示,40%溴酰·噻虫嗪种子处理悬浮剂和54%吡虫·氟虫腈悬浮种衣剂保护作用显著,菜心出苗后25 d的株高和鲜重与对照组相比均有增加,且差异显著。结果表明40%溴酰·噻虫嗪种子处理悬浮剂和54%吡虫·氟虫腈悬浮种衣剂对菜心种子具有较好的安全性,且对菜心苗期有良好的保护作用。 相似文献
45.
46.
五月季竹开花及复壮过程中DNA甲基化的MSAP分析 总被引:1,自引:0,他引:1
孙慧敏;顾小平;袁金玲;岳晋军 《植物研究》2013,33(6):723-730
以五月季竹为材料,采用MSAP技术对其开花及花后无性复壮过程中的DNA甲基化状况进行检测,分析其开花前后的甲基化动态,以揭示竹子开花及复壮过程中的表观遗传变化规律。结果显示:(1)五月季竹开花时其叶片甲基化水平降低,而在无性复壮产生不再开花新竹的过程中其叶片甲基化水平又逐渐回升;(2)与未开花竹株相比,五月季竹开花时有29.09%的甲基化位点发生了变异,其中有17.88%的位点在开花植株中发生了完全的去甲基化,远高于发生甲基化位点的比率;(3)复壮竹株与未开花竹株之间发生变异的位点数和所占比率,尤其是发生去甲基化的位点数和比率,低于开花竹株;(4)开花五月季竹花器官的甲基化水平低于叶片,同时有28.58%的位点发生了甲基化状态的改变,且同样以去甲基化为主。 相似文献
47.
Ethanolic sprays of gibberellins were applied to developing shoots of about 12-year-old Scots pine (Pinus sylvestris L.) grafts during the shoot elongation period in two consecutive years. Both male and female flowering was increased by these treatments in both years. The effect was particularly distinct in male flowering. However, different clones showed varying responses to the treatment. This variation was associated with both the genotype and the environmentally determined year-to-year fluctuation in flowering. Differences among clones were analysed further by introducing a model earlier developed for comparisons of the growth rhythm in various woody and herbaceous species. 相似文献
48.
Flowering requirements of Scandinavian Festuca pratensis 总被引:1,自引:0,他引:1
O.M. Heide 《Physiologia plantarum》1988,74(3):487-492
Flowering requirements of three Scandinavian cultivars of Festuca pratensis Huds, have been studied in controlled environments. At 3 and 6°C, primary induction was independent of photoperiod, while short days (8 h) were more effective than long days (24 h) at higher temperatures. The critical temperature for induction was about 15°C in short days and about 12°C in long days. Saturation of induction required 18–20 weeks of exposure to optimal conditions. At temperatures below 12°C both induction and initiation of inflorescence primordia took place in long days, while a transition to long days was required for inflorescence initiation after primary induction in short days. A minimum of 8 long-day cycles were required for flowering of plants primary induced in short days and saturation of flowering required more than 16 cycles. The critical photoperiod for secondary induction was about 13 h. High temperature (21°C) had some devernalization effect in primary induced plants, suppressing flowering compared with 15°C. 相似文献
49.
50.
Gibberellic acid signaling is required for ambient temperature‐mediated induction of flowering in Arabidopsis thaliana 下载免费PDF全文
Vinicius Costa Galvão Silvio Collani Daniel Horrer Markus Schmid 《The Plant journal : for cell and molecular biology》2015,84(5):949-962
Distinct molecular mechanisms integrate changes in ambient temperature into the genetic pathways that govern flowering time in Arabidopsis thaliana. Temperature‐dependent eviction of the histone variant H2A.Z from nucleosomes has been suggested to facilitate the expression of FT by PIF4 at elevated ambient temperatures. Here we show that, in addition to PIF4, PIF3 and PIF5, but not PIF1 and PIF6, can promote flowering when expressed specifically in phloem companion cells (PCC), where they can induce FT and its close paralog, TSF. However, despite their strong potential to promote flowering, genetic analyses suggest that the PIF genes seem to have only a minor role in adjusting flowering in response to photoperiod or high ambient temperature. In addition, loss of PIF function only partially suppressed the early flowering phenotype and FT expression of the arp6 mutant, which is defective in H2A.Z deposition. In contrast, the chemical inhibition of gibberellic acid (GA) biosynthesis resulted in a strong attenuation of early flowering and FT expression in arp6. Furthermore, GA was able to induce flowering at low temperature (15°C) independently of FT, TSF, and the PIF genes, probably directly at the shoot apical meristem. Together, our results suggest that the timing of the floral transition in response to ambient temperature is more complex than previously thought and that GA signaling might play a crucial role in this process. 相似文献