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ABSTRACT

Pest management professionals in California receive more customer complaints about Argentine ants than for any other urban ant pest. Fipronil, applied as a 30 × 30 cm band around the house foundation, has become the preferred treatment used to control these ants. Unfortunately, fipronil is now showing up in urban waterways at levels that are toxic to aquatic invertebrates. Our recent studies are aimed at mitigating insecticide runoff while still controlling the ant infestations. A high priority is preventing fipronil runoff from the driveway to the street, where it can flow into drains and from there to urban waterways. In this paper, two related studies address these issues. Not treating driveways with fipronil reduced by two to three orders of magnitude its runoff when compared with earlier studies. However, not treating the driveway can reduce efficacy of treatments. Granular bifenthrin, indoxacarb, botanicals, and a thiamethoxam ant bait were tested as supplemental treatments. The gel bait showed the best result as a supplement, but only after 8 weeks. We have reduced fipronil runoff while maintaining efficacy of the ant treatments.  相似文献   
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BACKGROUND: Spodoptera litura (F.) is a cosmopolitan pest that has developed resistance to several insecticides. The aim of the present study was to establish whether an emamectin‐selected (Ema‐SEL) population could render cross‐resistance to other insecticides, and to investigate the genetics of resistance. RESULTS: Bioassays at G1 gave resistance ratios (RRs) of 80‐, 2980‐, 3050‐ and 2800‐fold for emamectin, abamectin, indoxacarb and acetamiprid, respectively, compared with a laboratory susceptible population Lab‐PK. After three rounds of selection, resistance to emamectin in Ema‐SEL increased significantly, with RRs of 730‐fold and 13‐fold compared with the Lab‐PK and unselected (UNSEL) population respectively. Further studies revealed that three generations were required for a tenfold increase in resistance to emamectin. Resistance to abamectin, indoxacarb, acetamiprid and emamectin in UNSEL declined significantly compared with the field population at G1. Furthermore, selection with emamectin reduced resistance to abamectin, indoxacarb and acetamiprid on a par with UNSEL. Crosses between Ema‐SEL and Lab‐PK indicated autosomal and incomplete dominance of resistance. A direct test of a monogenic model and Land's method suggested that resistance to emamectin was controlled by more than one locus. CONCLUSION: Instability of resistance and lack of cross‐resistance to other insecticides suggest that insecticides with different modes of action should be recommended to reduce emamectin selection pressure. Copyright © 2010 Society of Chemical Industry  相似文献   
4.
茚虫威属于噁二嗪类杀虫剂,与大多数杀虫剂不同的是其进入害虫体内需要经活化代谢转变成N-去甲氧羰基代谢物(decarbomethoxylated metabolite,DCJW)后不可逆地阻断钠通道,进而发挥杀虫活性。茚虫威由于其作用机制不同于常见的使钠离子通道延迟关闭的菊酯类药剂而被广泛用于鳞翅目和一些同翅目、鞘翅目害虫的防治。抗药性是任何杀虫药剂使用后面临的问题,茚虫威也不例外,许多害虫对其产生了不同程度的抗性。昆虫对茚虫威产生抗性的机制包括酯酶活性、谷胱甘肽S-转移酶(glutathione S-transferase,GST)和P450活性的增加以及分子靶标F1845Y、V1848I、L1014P的突变,这些对茚虫威抗性机制的研究基本都是基于抗性种群和敏感种群开展的,需要进一步验证其对抗性研究的贡献度。针对我国田间害虫种群对茚虫威的抗性现状,及时实施对茚虫威有效的抗性治理是迫切的。对于茚虫威的抗性治理除了传统的杀虫药剂轮用、混用外,需要利用其作用机制特点开展抗性治理策略研究。一是充分利用其活化代谢的特点,开展组合药剂的研究应用;二是菊酯类药剂和茚虫威的作用机制均与钠离子通道有关,但是前者是使钠离子通道关闭延迟,而后者是阻断钠离子通道,开展相关基础研究,使菊酯类药剂与茚虫威合理地用于抗性治理中。本文综述了茚虫威的抗性现状、抗性机制与交互抗性、茚虫威的抗性风险评价,针对茚虫威的抗性特点提出了抗性治理策略。  相似文献   
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BACKGROUND: The goal of the research was to gather efficacy data required to introduce reduced-risk insecticides in sustainable control programs for European corn borer, Ostrinia nubilalis Hubner, on potato. RESULTS: Laboratory tests confirmed that sprays of indoxacarb and novaluron at recommended field rates are as effective as spinosad against neonate larvae of O. nubilalis. However, there is evidence that higher rates would enhance the inhibition of chitin synthesis by novaluron. The three insecticides showed ovilarvicidal activity when applied to O. nubilalis egg masses 2 days prior to black head stage. The ovicidal activity of spinosad and novaluron was almost twice that of indoxacarb. At the recommended field rates, the residues of the three insecticides displayed contact toxicity to O. nubilalis larvae. Spinosad residues 16 h old or less provided the highest immediate (24 h after exposure) contact mortality, followed by indoxacarb and then by novaluron. Also, residues of spinosad had faster contact efficacy than indoxacarb, which had faster efficacy than novaluron. CONCLUSION: Spinosad, indoxacarb and novaluron have ovicidal properties, which could enhance O. nubilalis management programs. However, the contact residual toxicity is limited in duration and would likely only play a minor role in O. nubilalis control.  相似文献   
6.
建立了反相条件下茚虫威在对映体水平上的液相色谱-串联质谱(LC-MS/MS)残留分析方法。采用基质匹配标准品的外标法定量,比较分析了基质分散萃取与固相萃取2种净化方法中基质效应的影响。番茄和葡萄样品均采用乙腈提取,NH2/Carb复合固相萃取小柱净化;水样直接采用C18-H固相萃取小柱富集净化。手性拆分的色谱条件为:Chiralpak AD-RH手性分离柱,以V(乙腈)∶V(水)=65∶35为流动相,柱温25 ℃,流速0.4 mL/min。结果表明:在0.005~0.5 mg/kg(水样为mg/L)添加水平范围内,茚虫威对映体在3种基质中的回收率在65.5% ~117.0%之间,相对标准偏差(RSD,n=5)为4.1% ~18.1%。对映体的检出限(LOD)为1.4~4.3 μg/kg(μg/L),定量限(LOQ)为4.7~14.2 μg/kg(μg/L)。方法操作简便,结果稳定可靠,可用于茚虫威对映体在番茄、葡萄和水样品中残留的分析。  相似文献   
7.
BACKGROUND: Non-repellent insecticides, including fipronil and indoxacarb, are becoming increasingly important for soil treatments to manage the eastern subterranean termite, Reticulitermes flavipes (Kollar). The effects of these insecticides on termite walking and tunneling behavior could significantly reduce their efficacy against colonies. RESULTS: Groups of R. flavipes were exposed to several concentrations of commercial formulations of fipronil and indoxacarb, and the ability of treated termites to tunnel in soil and walk was assessed. Increasing insecticide concentration resulted in a reduction in the ability of R. flavipes to walk, tunnel and form tunnel branches; the importance of these effects on the use of non-repellent insecticides is discussed. CONCLUSION: Exposure of R. flavipes to 1, 10 or 50 mg L−1 of fipronil or 50, 100 or 200 mg L−1 of indoxacarb significantly reduced termite walking and tunneling and the number of tunnel branches. Distance walked (ca 73 mm) by untreated control termites did not change over time for at least 16 h after treatment; control termites formed ca 150 cm of tunnels with ca 40 branches. Copyright © 2012 Society of Chemical Industry  相似文献   
8.
The effects of the oxadiazine insecticide indoxacarb and its N-decarbomethoxylated metabolite (DCJW) on tetrodotoxin-resistant (TTX-R) voltage-gated sodium channels in rat dorsal ganglion neurons were studied using the whole-cell patch clamp technique. Indoxacarb and DCJW suppressed the peak amplitude of action potentials, and DCJW exhibited a faster time course and higher potency than indoxacarb in the blocking effects. In voltage-clamp experiments, indoxacarb and DCJW suppressed TTX-R sodium currents in a time-dependent manner without a steady-state level of suppression. IC50 values for indoxacarb and DCJW on TTX-R sodium currents were estimated to be 10.7 and 0.8 microM after 25 min of bath application, respectively. DCJW was about 10 times more potent than indoxacarb in blocking TTX-R sodium currents. Although the suppressive effects of indoxacarb were partially reversible after washout with drug-free external solution, no recovery of sodium current was observed in DCJW treated neurons after prolonged washout. In current-voltage relationships, both indoxacarb and DCJW blocked the sodium currents to the same degree in the entire range of membrane potentials. The sodium conductance-voltage curve was not shifted along the voltage axis by indoxacarb and DCJW at 10 microM. In contrast, the steady-state inactivation curves were shifted in the hyperpolarizing direction by indoxacarb as well as by DCJW. Based on these results, it was concluded that indoxacarb and DCJW potently blocked the TTX-R sodium channel in rat DRG neurons with hyperpolarizing shifts of the steady-state inactivation curves, suggesting preferential association of the insecticides to the inactivated state of sodium channels. The small structural variation between indoxacarb and DCJW resulted in clear differences in potency for blocking sodium channels and reversibility after washout.  相似文献   
9.
The interactions between six insecticides (indoxacarb, cypermethrin, chlorpyrifos, azinphosmethyl, tebufenozide and chlorfenapyr) and three potential synergists, (piperonyl butoxide (PBO), S,S,S-tributyl phosphorotrithioate (DEF) and diethyl maleate (DEM)) were studied by dietary exposure in a multi-resistant and a susceptible strain of the obliquebanded leafroller, Choristoneura rosaceana (Harris). The synergists did not produce appreciable synergism with most of the insecticides in the susceptible strain. Except for tebufenozide, PBO synergized all the insecticides to varying degrees in the resistant strain. A very high level of synergism by PBO was found with indoxacarb, which reduced the resistance level from 705- to 20-fold when PBO was administered alone and to around 10-fold when used in combination with DEF. DEF also synergized indoxacarb, cypermethrin, chlorpyrifos, azinphosmethyl and tebufenozide in the resistant strain. DEM produced synergism of indoxacarb, chlorpyrifos, azinphos-methyl and chlorfenapyr in the resistant strain. DEM was highly synergistic to cypermethrin, and to some extent to tebufenozide in both the susceptible and resistant strains equally, implying that detoxification by glutathione S-transferases was not a mechanism of resistance for these insecticides. The high level of synergism seen with DEM in the case of cypermethrin may be due to an increase in oxidative stress resulting from the removal of the antioxidant, glutathione. These studies indicate that enhanced detoxification, often mediated by cytochrome P-450 monooxygenases, but with probable esterase and glutathione S-transferase contributions in some cases, is the major mechanism imparting resistance to different insecticides in C. rosaceana.  相似文献   
10.
应用30%茚虫威悬浮剂防治水稻稻纵卷叶螟(Cnaphalocrocis medinalis Guene).试验结果表明,该药剂对稻纵卷叶螟具有良好的防治效果,施药量在18、27、36 g(ai)/hm2浓度时,药后18d防治效果分别为82.08%、84.28%、87.68%,且持效期较长.试验期间未发现该药剂在供试剂量下对水稻产生药害,从使用成本与防治效果两方面综合考虑,生产上30%茚虫威悬浮剂的使用剂量以27~36 g(ai)/hm2为宜.  相似文献   
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