首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   1440篇
  免费   116篇
  国内免费   48篇
  2023年   12篇
  2022年   11篇
  2021年   22篇
  2020年   31篇
  2019年   22篇
  2018年   22篇
  2017年   23篇
  2016年   47篇
  2015年   51篇
  2014年   68篇
  2013年   78篇
  2012年   69篇
  2011年   68篇
  2010年   56篇
  2009年   57篇
  2008年   63篇
  2007年   50篇
  2006年   76篇
  2005年   73篇
  2004年   89篇
  2003年   45篇
  2002年   45篇
  2001年   42篇
  2000年   41篇
  1999年   38篇
  1998年   42篇
  1997年   34篇
  1996年   44篇
  1995年   30篇
  1994年   33篇
  1993年   22篇
  1992年   19篇
  1991年   25篇
  1990年   16篇
  1989年   20篇
  1988年   12篇
  1987年   14篇
  1986年   11篇
  1985年   15篇
  1984年   12篇
  1983年   10篇
  1982年   13篇
  1981年   8篇
  1980年   7篇
  1979年   2篇
  1978年   4篇
  1977年   3篇
  1976年   2篇
  1971年   1篇
  1967年   1篇
排序方式: 共有1604条查询结果,搜索用时 390 毫秒
851.
852.
Fine structural events in the mature stylar transmitting tissue ofsweet pepper (Capsicum frutescens L. var. grossum Bally) have been investigated byelectron microscope with regard to pollen tribe grwoth. The transmitting tissue consists of parenchymatous cells with large intercellular spaces filled with an electron densesubstance. The pollen tubes grow through the intercellular spaces in the intercellular substance. Cells of this tissue are rich in organelles, especially the rough and tubular ER, and numerous lomasomes near the plasma membrane. It is demonstrated that they function as secretory cells. On the other hand, the fact that the transmitting tissue contains many large amyloplastids with several starch grains in the cytoplasm and numerous globular protein bodies in vacuoles, indicates that the transmitting tissue mayhave some nutritive value for the growth of pollen tubes. The results obtained from this observation are in agreement with those of mostspecies reported by other authors and support the conclusion that the transmitting tissue is not a collenchyma tissue and the nature of intercellular substances is essentially same as that of the middle lamella.  相似文献   
853.
应用正交试验设计法研究基本培养基、植物生长调节剂种类及浓度对文心兰花梗茎段芽再生丛生芽诱导、增殖和生根培养的影响。筛选出最佳基本培养基为1/2 MS;最佳诱导培养基为1/2 MS+6-BA 5.0 mg/L+NAA 0.5 mg/L+蔗糖20 g/L;最佳增殖培养基为1/2 MS+6-BA 3.0 mg/L+NAA 0.5 mg/L+蔗糖30 g/L;最佳生根培养基为1/2 MS+IBA 0.05 mg/L+NAA 0.3 mg/L+香蕉泥100 g/L+蔗糖20 g/L。  相似文献   
854.
855.
Fucose-specific adhesins on germ tubes of Candida albicans   总被引:1,自引:0,他引:1  
Lectin-like adhesins of hyphal-form Candida albicans were investigated by conventional fluorescence microscopy, fluorescence microscopy with image analysis, spectrofluorimetry and flow cytometry. Labelling was done with neoglycoprotein probes consisting of sugars (fucose, mannose, glucose, galactose, lactose) covalently linked to bovine serum albumin (BSA), which itself was labelled with fluorescein. The fucose probe bound to both the yeast and germ-tube portions of hyphal-form cells, not especially at the tip, but in the adjacent region of the germ-tube portion. Probes with the other sugars did not label the hyphal-form cells. Fucose-probe binding to the cells was optimal at pH 5.0 in citrate buffer, and was a time-dependent reaction requiring 30–60 min and reaching saturation concentration at 100 μg ml−1. Each hyphal-form cell of C. albicans grown in 199 medium was calculated to have about 2×107 fucose probe-binding sites. There appeared to be no requirement for Ca2+ or Mg2+ in binding. Binding of the fucose probe to the hyphal-form cells was higher at 37°C than at 22°C or 4°C. Fluorescence intensity of the fucose-labelled yeast forms was not increased over the hyphal-form cells. A germ-tube-deficient mutant when exposed to hyphal-form growth conditions for 2 h showed much less binding of the fucose probe than the wild-type which produced germ tubes. Confirmation of specificity and the need for a carrier molecule was obtained by showing that Fuc-BSA (without fluorescein) effectively inhibited the binding of the fucose probe, although l-fucose itself was inactive, as was Gal-BSA.  相似文献   
856.
PP333对怀地黄试管苗形态及生理特性的影响   总被引:1,自引:0,他引:1  
李明军  徐鑫  张晓丽  杜琳   《广西植物》2007,27(2):250-254
研究PP333对怀地黄试管苗生长及一些生理指标的影响。通过单因子实验、比色法和愈创木酚法探讨PP333对试管苗的影响。结果表明,不同浓度PP333均促进试管苗芽的萌发,使根系粗壮,根数增加,低浓度PP333(0.01、0.05mg·L-1)促进试管苗茎的伸长生长,高浓度(0.1、2mg·L-1)抑制茎、叶生长,PP333浓度为2mg·L-1时壮苗效果最佳。PP333处理使试管苗生长中期叶片可溶性蛋白含量、POD活力提高。适宜浓度的PP333可以改变试管苗的生理特性,达到培育壮苗的目的。  相似文献   
857.
野葛的组织培养和植株再生   总被引:19,自引:1,他引:18  
野葛〔Puerarialobata(Wild.)Ohwi〕为豆科多年生缠绕藤本植物,分布遍及全国,主产南方[1],可药食两用,其块根肥厚,富含淀粉、蛋白质、钙、磷、铁及脂肪酸等,还含有多种异黄酮类化合物,对治疗心绞痛、高血压、冠心病,抑制肿瘤等效果显...  相似文献   
858.
The callose synthase (CalS) activity of membrane preparations from cultured Nicotiana alata Link & Otto pollen tubes is increased several-fold by treatment with trypsin in the presence of digitonin, possibly due to activation of an inactive (zymogen) form of the enzyme. Active and inactive forms of CalS are also present in stylar-grown tubes. Callose deposition was first detected immediately after germination of pollen grains in liquid medium, at the rim of the germination aperture. During tube growth the 3-linked glucan backbone of callose was deposited at an increasing rate, reaching a maximum of 65 mg h−1 in tubes grown from 1 g pollen. Callose synthase activity was first detected immediately after germination, and then also increased substantially during tube growth. Trypsin caused activation of CalS throughout a 30-h time course of tube growth, but the degree of activation was higher for younger pollen tubes. Over a 10-fold range of callose deposition rates, the assayed CalS activity was sufficient to account for the rate of callose deposition without trypsin activation, implying that the form of CalS active in isolated membranes is responsible for callose deposition in intact pollen tubes. Sucrose-density-gradient centrifugation separated a lighter, intracellular membrane fraction containing only inactive CalS from a heavier, plasma-membrane fraction containing both active and inactive CalS, with younger pollen tubes containing relatively more of the inactive intracellular enzyme. The increasing rate of callose deposition during pollen-tube growth may thus be caused by the transport of inactive forms of CalS from intracellular membranes to the plasma membrane, followed by the regulated activation of these inactive forms in this final location. Received: 1 December 1998 / Accepted: 21 January 1999  相似文献   
859.
Jaborosa integrifolia exhibits stigma-height polymorphism. There are individuals with flowers where anthers and stigma are at the same height but the rule is variable herkogamy, the most common type (75%) being that with an exerted stigma. Self- and cross-tubes did not differ in their capability to reach the ovary (t = –0.67,P < 0.53); they had a high growth rate (6.95 ± 2.28 mm h–1). There is not autogamy but mostly self-incompatibility. Fruits from controlled cross-pollination showed the highest seed set and seed viability. The nectar sugar is characterized by a similar amount of glucose and fructose, and by the absence of sucrose. Although nectar secretion was continuous throughout the life of the flower, most nectar was secreted during the first 24 h after flower opening. Nectar production costs appear to be lower than in other species since nectar secretion is neither inhibited after a removal (i.e. a pollinator visit) nor reabsorbed as the flower ages. Sphingids visit the flowers mainly after midnight. They insert their proboscis down to the base of the corolla tube to reach the nectar. The upper limit to fruit production is set by pollinator visits. Fruits produced from open-pollinated flowers are often predated by numerous larvae (mainly lepidopteran ones). Considering that this species is mostly self-incompatible and pollination is limited, that each plant displays only a low number of flowers throughout the flowering season, and that there is a high rate of fruit predation, it is not surprising that fruits ofJ. integrifolia are so rare.  相似文献   
860.
杜仲休眠枝条中多糖颗粒变化的超微结构研究   总被引:3,自引:0,他引:3  
在对杜仲(Eucommia ulmoides Oliv.)形成层休眠期枝条的超微结构研究中发现,在筛管分子的筛板附近有一种复合球形体。细胞化学研究证明,这是一种多糖颗粒,但不同于枝条其他薄壁细胞中的多糖颗粒,而与细胞壁中的多糖相似。这种复合球形体只出现于形成层生理休眠期的筛分子中,而在被动休眠期和活动的筛分子中则看不到。  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号