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541.
542.
棉铃虫滞育的遗传方式 总被引:6,自引:0,他引:6
采自北京和湖北省武穴市的棉铃虫(HelicoverpaarmigeraHubner)在24℃,12:12(L:D)光周期下的滞育充分别为80.32%和53.00%对北京群的滞育性和武穴种群的滞育不敏感性分别进行5代和14代选育,北京种群(B)的滞育反应无明显变化,而武穴种群(W)则稳定在20%~30%之间,表明武穴种群存在较大的遗传异质性,对二者的杂交试验显示,显性系数DWB和DBW分别为-0.2 相似文献
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545.
研究测定了棉铃虫对 30种氨基酸、10种糖类和 4种棉花次生物质的取食选择性。结果显示初孵幼虫对0.1g/ml的L-苏氨酸、DL-2-氨基-n-丁酸、L-亮氨酸、L-缬氨酸、DL-瓜氨酸、L-丙氨酸、D-海藻糖、D-果糖以及棉花次生物质儿茶精、棉酚、槲皮素表现出较强的趋性反应 ,但将L-苏氨酸、L-亮氨酸、D-瓜氨酸、L-缬氨酸、L-苯丙氨酸以0.009g/ml的浓度、槲皮素和10种糖物质以0.025g/ml的浓度分别掺入人工饲料中,5日龄幼虫仅对D-海藻糖表现出高的取食选择性 相似文献
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547.
A primitive cotton(Gossypium hirsutum L.) accession, V-64, from the Caribbean Islands was bioassayed for antibiosis against pests of this crop in comparison with
the commercial strains Acala SJ-2 and Pima S-5. V-64 reduced weight gain and leaf consumption ofSpodoptera littoralis andHelicoverpa armigera, and significantly reduced oviposition ofBemisia tabaci. The leaf pigment glands in V-64 were larger and more abundant than in the commercial strains, and the feeding ofH. armigera on these glands was avoided, indicating that the glands probably constituted the major resistance character in V-64.
Contribution from the Agricultural Research Organization. No. 3187-E, 1991 series. 相似文献
548.
转Bt基因抗虫棉棉铃虫防治技术研究 总被引:9,自引:5,他引:4
1995~1997年就转Bt基因抗虫棉对棉铃虫的抗性及棉铃虫的防治技术进行了研究。结果表明,抗虫棉对棉铃虫具有很强的内在抗性,对初孵幼虫致死率达90%以上,对幼虫的生长发育影响严重,其毒力随幼虫龄期的增大而降低。在棉铃虫大发生年份,对二、三代棉铃虫不进行药剂防治则显著减产。初步提出抗虫棉的棉铃虫防治策略为:二代以保棉株生长点为主,三代要重点防治以保蕾铃。其防治指标是:二代棉铃虫百株累计卵量200~300粒,三代百株累计卵量80~120粒。 相似文献
549.
Elevated oxidative detoxification is a major mechanism responsible for pyrethroid resistance in Helicoverpa armigera from Asia. Constitutive overexpression of CYP9A12 and CYP9A14 was associated with pyrethroid resistance in the YGF strain of H. armigera. CYP9A12 and CYP9A14 were functionally expressed in the W(R) strain of yeast (Saccharomyces cerevisiae) transformed with a plasmid shuttle vector pYES2. The cell lysates prepared from yeast transformed with CYP9A12 and CYP9A14, respectively, exhibited considerable O-demethylation activities against two model substrates p-nitroanisole (0.59 and 0.42 nmol p-nitrophenol min−1 mg protein−1) and methoxyresorufin (2.98 and 5.41 pmol resorufin min−1 mg protein−1), and clearance activity against the pyrethroid esfenvalerate (8.18 and 4.29 pmol esfenvalerate min−1 mg protein−1). These results provide important evidence on the role of CYP9A12 and CYP9A14 in conferring pyrethroid resistance in H. armigera, and also demonstrate that the yeast expression system can provide necessary redox environment for insect P450s to metabolize xenobiotics. 相似文献
550.
The Helicoverpa armigera cathepsin B-like proteinase (HCB) has been shown to have a wide spectrum of substrates. It has been involved in the degradation of yolk protein during embryonic development and also in the decomposition of the adult fat body. To study the possibility of using HCB to improve the insecticidal activity of bioinsecticides, it was inserted into the pFASTBACDUAL-green fluorescent protein (GFP) donor plasmid under the strong polyhedrin promoter, and the polyhedrin gene was retained behind the HCB gene so that the virus could orally infect the host and survive in the natural environment. After the recombinant plasmid transfected the Sf21 cells, the recombinant baculovirus Autographa californica multiple nucleocapsid nucleopolyhedrovirus (AcMNPV)-GFP-HCB-Polh+ was produced. A 37-kDa recombinant procathepsin B was expressed in AcMNPV-GFP-HCB-Polh+-infected Sf21 cells and processed into 29/25-kDa mature forms. Gelatin zymography revealed that the proteolytic activities of the recombinant HCB and other proteases were activated or enhanced by HCB in AcMNPV-GFP-HCB-Polh+-infected larvae. Green fluorescence was observed earlier and was more intense in AcMNPV-GFP-HCB-Polh+-infected larvae than in HCB-free AcMNPV-GFP-Polh+-infected ones that were infected at the same time; this indicated that the AcMNPV-GFP-HCB-Polh+ virus spreaded faster in larvae than the AcMNPV-GFP-Polh+ virus. A bioassay revealed that infection with the AcMNPV-GFP-HCB-Polh+ virus shortened the median survival time of H. armigera larvae by 12 h as compared with those infected with the AcMNPV-GFP-Polh+ or the wild-type AcMNPV virus. These results suggest that HCB may possibly play a role in the recombinant virus in improving the rate of killing larvae. 相似文献