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21.
Summary

Tree species adapted to the climatic conditions of the northern boreal and subarctic vegetation zones have a capacity to develop a very high level of frost hardiness, even to survive the temperature of liquid nitrogen in midwinter. Proper timing of hardening, as well as of dehardening, is crucial for winter survival of these species. In northern tree species, cessation of apical elongation growth and bud set is a prerequisite for developmental and metabolic processes leading to hardening, and this chain of events is induced by photoperiod. The northern tree species are closely adapted to the local light climate and display photoperiodic ecotypes. The critical photoperiod is under genetic control and increases with increasing latitude of origin of the eco-type. The photoperiod is probably perceived by the phytochrome system, but the role of other pigment systems, like cryptochrome, has not been studied in woody plants. Phytochrome genes have been cloned from both conifers and deciduous species, but so far we do not have any information about possible differences between photoperiodic ecotypes at the phytochrome level. Northern and southern ecotypes have different responses to red:far red ratios, which could indicate differences in composition of their phytochrome systems, for example, the proportions of phytochrome A and B. Both phytochrome A and phytochrome B can be involved in photoperiodic responses. Experiments with transgenic hybrid aspen suggest that responses to photoperiod could be affected by the amount of phytochrome A present in plants. In deciduous species, the plant hormone gibberellin A1 (GA1) can completely substitute for a long photoperiod, and short day induced cessation of growth is preceded by a significant reduction of GA1 levels, particularly in the elongation zone. Photoperiodic control of GA metabolism is supported by several studies, but very little is known about the interaction between phytochrome and GA metabolism and/or responsiveness to GA1. Although our knowledge is still very fragmentary, available results suggest that cessation of growth and initiation of hardening in trees can be controlled both through the phytochrome and the GA mediated systems. Research with tree species is a tedious and slow process, but with the emerging new methods and approaches, we may expect exciting new results in the near future.  相似文献   
22.
分蘖与株高是禾本科草类植物重要的农艺性状,明确参与调控分蘖与株高的基因类型对牧草和草坪草分子辅助育种具有重要意义。以表型差异明显的两个高羊茅品种“Kentucky-31”(K31)和“Regenerate”为材料,旨在构建高羊茅分蘖节转录组图谱,挖掘在分蘖节部位调控生长发育相关的差异表达基因(differentially expressed genes,DEGs)。基于高通量测序技术平台Illumina HiSeq 2500×Miseq 300进行转录组测序,并将得到的数据进行de novo组装,结果共获得77872条单基因簇(unigene)。将获得的unigenes与非冗余蛋白数据库(non-redundant protein database,NR)、蛋白质数据库(universal protein,Uniprot)、基因本体数据库(gene ontology,GO)、东京基因与基因组数据库(kyoto encyclopedia of genes and genomes,KEGG)以及直系同源蛋白簇(clusters of orthologous groups,COG)数据库进行比对,结果显示:分别有59927、40213、44447、15146和13767条unigenes成功获得注释。“Regenerate”与“K31”对比有1573个上调DEGs和1441个下调DEGs。GO富集分析发现,DEGs主要富集在细胞、细胞组分、大分子复合物组装等生物过程。DEGs中共注释到42个差异表达转录因子,主要包括TCP、WRKY和ARF等19种类型。还注释到与8类植物激素相关的DEGs,包括生长素、细胞分裂素、脱落酸、赤霉素、乙烯、油菜素甾醇、水杨酸和茉莉酸。利用实时荧光定量PCR对DEGs进行表达模式验证,发现其与RNA-Seq测序结果一致,证实了测序结果的准确性。研究结果丰富了高羊茅的转录组序列资源,初步获得控制株高及分蘖发育的候选因子,为进一步开展基因功能及分子育种研究提供了理论支持。  相似文献   
23.
关于激素在果实生长发育过程中的作用 ,前人曾进行过大量的研究 ,并取得了许多宝贵的成果[1,2 ] ,而对银杏 (GinkgobilobaL .)种子的相关研究却很少。银杏作为一种古老的裸子植物 ,其种子的生长发育与一般的裸子植物又有不同 ,它的胚珠直接着生在短枝上 ,没有了一般裸子植物的球果构造 ,从表面上看很类似于杏 (Armeniacaspp .)、桃 (Amygdalusspp .)等的生长发育过程。本文从分析银杏种子生长发育的一般特点出发 ,研究了银杏种子生长发育与内源激素含量的关系 ,旨在探索银杏种子生长发育的一般规律 ,…  相似文献   
24.
以小叶杨(Populussimoniicarr.)原生质体培养的愈伤组织为供试材料,用高压波相色谱法(HPLC),测定它们在四种不同分化培养基上四大类内源激素(IAA,GA3,CTK,ABA)的含量变化,并检定有关N的生化反应。结果表明,不同分化培养基上的愈伤组织中内源激素含量和种类差异很大。导致细胞分裂素(CTK)含量高,种类多以及细胞分裂素与生长素的比值(CTK/IAA)高的处理,有利于愈伤组织分化;但若愈伤组织中含有内源脱落酸(ABA),则抑制分化。测定结果还表明,小叶杨原生质体培养的愈伤组织分化过程中,其硝酸还原酶活力与氨基态N含量互为消长。分化频率高的愈伤组织中,硝酸还原酶活力低,而氨基态N含量高.  相似文献   
25.
To determine the relationship between female sterility of Pinus tabulaeformis Carr. and plant hormones, content changes of several endogenous plant hormones in a female-sterile clone and a normal clone were analyzed during the key period of female gametophyte abortion in mutant clones. The change of ABA content showed a similar pattern between normal and mutant clones, but the ABA content of the mutant clone was always much higher than that of the normal clone. In the normal clone, the IAA content decreased significantly at the early stage of the period and reached its minimum during the first ten days of April and stabilized thereafter. The endogenous ZR levels increased sharply at the early stages and reached a maximum in the middle of April, then decreased dramatically. The IAA and ZR contents of the mutant clone did not change perceptively through the entire period. We conclude that the high levels of ABA and the deficit of IAA and ZR may be the reasons of female gametophyte abortion in the female-sterile clones of P. tabulaeformis.  相似文献   
26.
采用石蜡切片技术和酶联免疫吸附法(ELISA),以银杏幼胚为外植体,添加0,1和5 mg/L AgNO3作处理,观察21 d内愈伤组织的形成过程,测定内源激素吲哚乙酸(IAA)、保幼激素类似物(ZR)、赤霉素(GA)和脱落酸(ABA)的变化,分析AgNO3对银杏幼胚愈伤组织分化潜能的影响。结果表明:根据解剖结构愈伤形成可分为4个阶段。第1阶段(0~7 d),IAA升高,ABA降低,表皮细胞启动脱分化。第2阶段(≥7~11 d),4种激素浓度均升高,愈伤组织和细胞团初步形成。第3阶段(≥11~16 d),GA、ABA大幅降低,细胞团大量形成。第4阶段(≥16~21 d),ABA骤降、GA迅速上升,愈伤组织和细胞团增殖。1 mg/L AgNO3处理下分生细胞团种类最多,其次为5mg/L处理,0 mg/L处理最少。研究认为,银杏幼胚愈伤组织具有较强的分化潜能,AgNO3能影响其内源激素的平衡,调控分化方向。  相似文献   
27.
Two hundred eight Angus-crossbred heifers (291 ± 23 kg) from four sources were used in a randomized complete block design. The objective of the study was to determine the effects of implant strategy and Zn supplementation on performance, carcass characteristics, muscle fiber diameter, and mineral status of heifers. Heifers were assigned to a 2 × 2 factorial study for 168 d, and factors included Zn and implant (IMP). Heifers were supplemented Zn (mg/kg dry matter [DM]; ZnSO4) at national (30; NRC) or industry (100; IND) recommendations. Implant strategies (Merck Animal Health, Madison, NJ) included extended-release Revalor-XH on day 0 (REV-XH; 20 mg estradiol + 200 mg trenbolone acetate) containing four uncoated pellets and six coated pellets or the uncoated implant Revalor-200 on day 0 and again on day 91 (REV-200; 20 mg estradiol + 200 mg trenbolone acetate). Heifers were blocked by weight within source to pens of five or six heifers per pen (nine pens per treatment). A corn silage-based diet was fed during the growing period (days 0–55) followed by transition to a corn-based finishing diet. Weights were taken consecutively on days −1/0, 55/56, and 167/168. Liver and muscle from the longissimus thoracis were collected from one heifer per pen on days −5, 14, 105, and 164. Data were analyzed via Mixed Procedure of SAS. Average daily gain (ADG) and liver mineral used Period as the repeated effect. Corresponding to periods of high hormone payout from each implant, days 0–28 and 91–120 ADG were greatest for REV-200, whereas REV-XH numerically peaked during days 56–91 (IMP × Period; P = 0.02). Day 91 IND body weight tended to be heavier (P = 0.06) and day 120 body weight was heavier (P = 0.05) than NRC heifers. No effect of Zn or IMP on final body weight was observed (P ≥ 0.21). Muscle fiber cross-sectional diameter on day 164 was greater (P = 0.05) in IND than NRC. Liver Mn concentrations decreased by day 14 regardless of implant, though days 105 and 164 concentrations were lesser for REV-200 than REV-XH (IMP × Period; P = 0.02). No effects of Zn, IMP, or the interaction were observed for carcass-adjusted gain to feed, days 0–168 DM intake, hot carcass weight, or ribeye area (P ≥ 0.11). The nominal differences in performance between implant strategies suggest that extended-release implants may be an effective implant strategy to replace re-implant programs in heifers, whereas the improved performance of heifers fed IND vs. NRC during times of peak hormone payout suggests a role for Zn in periods of rapid growth.  相似文献   
28.
【目的】分析梅PmARF17的生物学功能,探究梅花发育进程中其表达丰度与内源激素动态变化的关系,为梅花发育的调控研究提供依据。【方法】以梅品种‘大嵌蒂’为试材,克隆PmARF17,利用生物信息学软件分析基因结构、系统进化及其与其他物种同源蛋白的差异;亚细胞定位确定PmARF17蛋白在细胞中作用的部位;以梅品种‘大嵌蒂’和‘龙眼’不同发育阶段的花芽、叶芽、花器官为试材,利用qRT-PCR检测PmARF17时空表达模式,通过UPLC法测定IAA、GA3、ABA、ZT含量的动态变化,并与PmARF17的表达进行相关性分析;克隆PmARF17启动子,分析启动子的顺式作用元件,利用瞬时表达解析PmARF17与GA3的调控模式。【结果】从梅品种‘大嵌蒂’中克隆得到PmARF17,系统进化树分析表明PmARF17蛋白与其他植物的ARF蛋白序列高度同源;亚细胞定位表明其作用于细胞核和细胞膜上;qRT-PCR表达和内源激素含量的相关性分析表明,PmARF17的表达与IAA含量的变化趋势没有明显的相关性。PmARF17在雌蕊完好花芽中的表达水平相对不完全花芽显著上调,而GA3含量与PmARF17的表达趋势一致。ABA和ZT含量总体上与PmARF17的表达呈相反的趋势,表明两者可能抑制PmARF17的表达。PmARF17启动子含有GA顺式元件,且具有启动活性和组织表达特异性,在花瓣、雄蕊及根部特异表达。【结论】 PmARF17可能是梅花发育的正调控基因,促进梅雌蕊的正常发育。PmARF17的表达可能受到GA3的正调控,其可能通过作用于雄蕊和花瓣,进而影响梅的雌蕊发育进程。  相似文献   
29.
【目的】VQ基因家族在植物生长、发育以及对生物或非生物胁迫反应中发挥重要功能。在全基因组尺度上,全面鉴定苦荞(Fagopyrum tataricum L. Gaertn.)VQ(FtVQ)基因家族,分析其在苦荞叶斑病原——互格链格孢(Alternaria alternata)和黑孢霉(Nigrospora osmanthi)侵染和防御相关激素——水杨酸(SA)、茉莉酸(JA)、乙烯(ET)处理下的表达模式,为深入解析苦荞VQ基因家族在植物抗病防御中的功能及机理奠定基础,同时为优良基因资源发掘及抗病品种改良提供线索。【方法】基于VQ保守结构域的隐马尔可夫文件(PF05678),采用HMMER 3.0对苦荞平苦一号基因组数据库进行比对搜索,鉴定VQ基因;通过DNAMAN、MapInspect、MEGA、MEME、OrthoFinder、PLACE等生物信息学工具分析基因结构、染色体分布、启动子顺式元件、蛋白质理化性质、蛋白质保守基序、蛋白质亚细胞定位和蛋白质系统进化关系;采用实时荧光定量PCR(qPCR)方法分析苦荞叶VQ基因在病原侵染或激素处理下的表达模式。【结果】从苦荞基因组中鉴定获得28个VQ基因,大小为566—1 454 bp,均无内含子,不均一地分布在8条染色体上。根据它们在染色体上的物理位置,命名为FtVQ1FtVQ28。每一个FtVQ蛋白含有1个VQ基序——FxxxVQx(L/F/I/V/A/Y)TG(x代表任意氨基酸)。亚细胞定位预测表明,21个FtVQ蛋白定位在细胞核中,其余定位在叶绿体或细胞质中。根据蛋白质氨基酸序列与保守结构基序,FtVQ蛋白归类于5个亚家族,亚家族内基因结构和蛋白质基序相对保守。基因重复分析表明,苦荞基因组中有8对VQ旁系同源基因,均为大片段重复基因,提示大片段基因重复在FtVQ基因家族数量扩张中发挥主要作用;它们的非同义突变和同义突变的比值(Ka/Ks)均小于1,提示重复基因在进化中经历了纯化选择。启动子顺式元件预测表明,所有FtVQ基因启动子含有BIHD1OS、CGTCA、ERELEA4、W-box和类W-box等病原或SA、JA、ET反应元件,尤其在FtVQ10FtVQ14FtVQ15FtVQ22FtVQ23FtVQ27的启动子区域密集程度更高。qPCR分析显示,在可检测的20个FtVQ基因中,有55%—70%的基因为病原或激素处理下的差异表达基因(DEGs),其中72.7%—85.7%的DEGs的表达显著上调。【结论】苦荞基因组拥有28个VQ基因成员,部分VQ基因可能参与了苦荞对叶斑病原的抗性反应。  相似文献   
30.
Low protein provision in utero and post‐partum may induce metabolic disorders in adulthood. Studies in mink have mainly focused on short‐term consequences of low protein provision in utero whereas the long‐term responses to low protein (LP) provision in metabolically programmed mink are unknown. We investigated whether low protein provision in utero affects the long‐term response to adequate (AP) or LP provision after weaning in male mink. Eighty‐six male mink were exposed to low (19% of ME from CP; crude protein) or adequate (31% of ME from CP) protein provision in utero, and to LP (~20% of ME from CP) or AP (30–42% of ME from CP) provision post‐weaning. Being metabolically programmed by low protein provision in utero did not affect the response to post‐weaning diets. Dietary protein content in the LP feed after weaning was below requirements; evidenced by lower nitrogen retention (p < 0.001) preventing LP mink from attaining their growth potential (p < 0.02). LP mink had a lower liver, pancreas and kidney weight (p < 0.05) as well as lower plasma IGF‐1 concentrations at 8 and 25 (p < 0.05) weeks, and a higher incidence of hepatic lipidosis at 25 weeks (p < 0.05). Furthermore, LP mink had a higher body fat (p < 0.05) and lower body CP content (p < 0.05) at 50 weeks of age. It is concluded that some effects of low protein provision in utero can be alleviated by an adequate nutrient supply post‐partum. However, long‐term exposure to low protein provision in mink reduces their growth potential and induces transient hepatic lipidosis and modified body composition.  相似文献   
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