Effects of insecticides on plant-growth-promoting activities of phosphate solubilizing rhizobacterium Klebsiella sp. strain PS19

In this study, four technical grade insecticides, fipronil, pyriproxyfen, imidacloprid and thiamethoxam were applied at the recommended and the higher doses to investigate their effects on plant growth-promoting activities of phosphate-solubilizing Klebsiella sp. strain PS19, isolated from mustard rhizosphere. All tested insecticides displayed a concentration-dependent inhibition in plant growth promoting traits, like, inorganic phosphate solubilization, biosynthesis of phytohormones and siderophores, of rhizobacterial strain PS19. For example, the phosphate-solubilizing activity of Klebsiella sp. PS 19 was reduced maximally by 95%, at 3900 μg l⁻¹ pyriproxyfen over control. At the recommended rate, the magnitude of toxicity of insecticides to plant growth promoting traits was less severe compared to the higher doses. The sequence of insecticide-toxicity expressed as percent decrease, determined at highest dose rate of each insecticide, over control was: pyriproxyfen (95) = imidacloprid (95) > thiamethoxam (94) > fipronil (85), for phosphate-solubilizing activity while for salicylic acid (SA) it was: thiamethoxam > pyriproxyfen = imidacloprid > fipronil. The impact of the highest dose rate of insecticides on 2,3-dihydroxybenzoic acid (DHBA) was almost equal to those observed for SA. Thiamethoxam decreased the indole acetic acid (IAA) synthesis maximally by 86% whereas fipronil had least toxicity and reduced it by 67% relative to the control. Among the experimental insecticides, pyriproxyfen at 3900 μg l⁻¹ in general, had the greatest toxic effects for plant growth promoting activities of the test strain. The study inferred that insecticides affect the plant beneficial activities of rhizobacteria adversely. These findings are likely to add a new insight into the pest management practices.     

Effect of temperature on toxicity of pyrethroids and endosulfan, activity of mitochondrial Na-K-ATPase and Ca-Mg-ATPase in Chilo suppressalis (Walker) (Lepidoptera: Pyralidae)

The toxicity of deltamethrin, bifenthrin, and endosulfan to the fourth-instar larvae of rice stem borer, Chilo suppressalis (Walker), was measured at 17, 27, and 37 °C. The three insecticides all displayed a positive temperature coefficient between 17 and 37 °C. The temperature coefficients of deltamethrin, bifenthrin, and endosulfan were 5.59, 1.68, and 2.85, respectively. However, temperature coefficients of deltamethrin and bifenthrin between 17 and 27 °C and between 27 and 37 °C varied. The inhibition of the above three insecticides to mitochondrial Na⁺-K⁺-ATPase and Ca²⁺-Mg²⁺-ATPase from the fourth-instar larvae of rice stem borer was determined at 17, 27, and 37 °C. The inhibition of deltamethrin to the specific activities of Na⁺-K⁺-ATPase and Ca²⁺-Mg²⁺-ATPase showed a negative temperature coefficient, but endosulfan exhibited a positive temperature coefficient. Inhibition of bifenthrin exhibited the contrary temperature coefficients between Na⁺-K⁺-ATPase and Ca²⁺-Mg²⁺-ATPase and a negative temperature coefficient for the former and a positive temperature coefficient for the later.     

Surface contact toxicity and synergism of several insecticides against different stages of the tropical bed bug, Cimex hemipterus (Hemiptera: Cimicidae)

BACKGROUND: Five formulated insecticides (lambda‐cyhalothrin at 10 mg m^?2, bifenthrin at 50 mg m^?2, fipronil at 10 mg m^?2, fenitrothion at 50 mg m^?2, imidacloprid at 5 mg m^?2) and one active ingredient (DDT at 500 mg m^?2) were evaluated using a surface contact method against early and late instars and adults of two strains of the tropical bed bug, Cimex hemipterus (F.). Synergism of lambda‐cyhalothrin and fipronil using piperonyl butoxide (PBO) was also assessed. RESULTS: The order of susceptibility of different stages of bed bugs was as follows: early stage ? lambda‐cyhalothrin > bifenthrin = imidacloprid > fipronil > fenitrothion > DDT; late stage—lambda‐cyhalothrin > bifenthrin > fenitrothion > imidacloprid > fipronil > DDT; adult—lambda‐cyhalothrin > imidacloprid > bifenthrin > fenitrothion > fipronil > DDT. The late instars exhibited significantly higher LT₅₀ among the life stages. The addition of PBO to fipronil increased the susceptibility of the insects. CONCLUSIONS: Lambda‐cyhalothrin, bifenthrin, fenitrothion and fipronil at the recommended application rates were effective against C. hemipterus. Although imidacloprid demonstrated good initial response against C. hemipterus, the insects showed substantial recovery 72 h post‐treatment. The late instars (fourth and fifth instars) should be used as the model for toxicological evaluation. Copyright © 2011 Society of Chemical Industry     

3种白蚁防治药剂对散白蚁的控制效果观察

2010年-2012年应用吡虫啉10%悬浮剂、联苯菊酯5%悬浮剂和氟虫腈0.5%粉剂等3种白蚁防治药剂对危害房屋建筑的散白蚁进行了针对性处理,对其防治效果进行了观察和统计研究。结果表明：吡虫啉10%悬浮剂、联苯菊酯5%悬浮剂、氟虫腈0.5%粉剂对房屋建筑散白蚁危害的控制率分别为：85.30%、84.01%、80.33%,具有较好的防治效果,且吡虫啉10%悬浮剂、联苯菊酯5%悬浮剂防效均显著高于氟虫腈0.5%粉剂。此外,对3种白蚁防治药剂处理后再次发生蚁害的情况进行了分析。     

Neonicotinoid insecticides imidacloprid and clothianidin affect differently neural Kenyon cell death in the cockroach Periplaneta americana

The intracellular toxicity of the neonicotinoid insecticides imidacloprid and clothianidin was studied on cockroach Periplaneta americana Kenyon cells using the trypan blue exclusion test and the adenylate kinase (AK) detection reagent. To evaluate cytotoxicity, Kenyon cells were exposed to different concentrations (1, 5, 10, 50 and 100 μM) of both imidacloprid and clothianidin at different delays (1, 3, 5, 8 and 24 h). Our data show that both imidacloprid and clothianidin decreased cell viability, with a more pronounced effect following imidacloprid exposure. Indeed, a significant decrease of cell viability was observed for 50 and 100 μM imidacloprid at 8 and 24 h, with trypan blue exclusion test. Study of the AK activity revealed that 50 and 100 μM imidacloprid induced an increase of AK activity, except for 50 μM at 24 h whereas at the same concentrations, clothianidin induced a transient effect at 5 and 8 h. According to previous studies showing that imidacloprid was a partial agonist and clothianidin a full agonist of insect nicotinic acetylcholine receptors, we demonstrated that both imidacloprid and clothianidin were also able to induce distinct intracellular toxic effects.     

Biochemical and physiological changes on Bacillus thuringiensis cotton after imidacloprid foliar spray

Bacillus thuringiensis cotton is a variety of cotton genetically modified to contain a gene derived from B. thuringiensis bacteria; which results in expression of toxin protein that confers resistance to bollworm complex (the most destructive pest of cotton). Introduction of Bt cotton lowered the need of insecticides, but still a number of insecticides are used for other insects like jassids, whitefly, aphids and tobacco caterpillar to which Bt gene does not provide effective control. Imidacloprid (tradename Imidacel 17.8 SL) is an insecticide designed for control of these major sucking/piercing insects that affect cotton. So in the present work we studied the post effect of imidacloprid insecticide on plant health of three Bt cotton hybrids (RCH-134, JKCH-1947, NCEH-6R) as there are reports of this insecticide causing growth and yield enhancements in absence of insect pests. Imidacloprid was first sprayed at recommended concentration (40 ml/acre) on 3 months old plants sown in randomly designed plots with three replications of each hybrid. The spray was repeated three times at 10 days interval. The level of B. thuringiensis gene expression, peroxidase activity and total phenols was measured on third day after every spray in leaves along with growth and yield of plants. The insecticide has shown to increase the level of B. thuringiensis protein, peroxidase enzyme activity, total phenols, height, number of bolls retained on plants and yield. These observations suggested that the imidacloprid treated plants showed better growth and development, thereby imidacloprid has growth enhancing effect on Bt cotton plants in addition to its insecticidal properties.     

Behavioral effects of acute exposure to the insecticide fipronil

The effects of fipronil (Frontline® Top Spot) were investigated in 40 days old rats utilizing open field (OF), hole-board (HB) and elevated plus-maze (EPM) apparatus. Rats (N = 15) received topical application of fipronil (70, 140 and 280 mg/kg) in the neck region and behavior was tested 3 h after administration. Animals treated with corn oil (vehicle) were used as controls. In the OF test animals treated with fipronil at 140 mg/kg showed increased rearing, whereas animals exposed to 280 mg/kg showed increased freezing, grooming, and rearing. In the HB test fipronil at 280 mg/kg increased head-dip and head-dipping behaviors. In the EPM test the only observed effect was increased number of entries in both open and closed EPM arms in animals treated with 280 mg/kg. In conclusion, dermal exposure to fipronil causes effects related to emotionality, fear, and exploratory activity; results add strength to the growing concern that pirazole insecticides can be neurotoxic to humans.     

Effect of synthetic insecticides on the larvae of <Emphasis Type="Italic">Coccinella septempunctata</Emphasis> from Greek populations

Coccinella septempunctata L. is one of the most abundant ladybird species in Greece, preying on several aphid species and other arthropods, of which many are pests of cultivated plants. These pests are usually controlled with chemical insecticides. During this process, however, beneficials are also exposed to pesticides. The development of Integrated Pest Management (IPM) programs against aphids requires the evaluation of the effects of insecticides on beneficial insects. We evaluated the LD₅₀ of imidacloprid, acetamiprid, bifenthrin and deltamethrin on first, second, third and fourth instar larvae of C. septempunctata by topical application. Moreover, we studied their sublethal effects (LD₁₀) on the development, weight and prey consumption of fourth instar larvae. The topical application bioassays showed that deltamethrin and bifenthrin were highly toxic to all larval instars, whereas imidacloprid and acetamiprid were less toxic to fourth instar larvae. The LD₁₀ dose significantly affected, developmental time, adult weight and daily predation. These results show the importance of assessing potential effect of insecticides on C. septempunctata for developing effective IPM programs of aphids in Greece.     

山东省绿盲蝽田间种群对六种杀虫剂的敏感性监测

为了解山东地区绿盲蝽对常用杀虫剂的敏感性变化情况,于2010—2012年采用玻璃管药膜法监测山东聊城、菏泽、滨州、德州地区绿盲蝽田间种群对马拉硫磷、毒死蜱、灭多威、丁硫克百威、联苯菊酯和氟虫腈等6种杀虫剂的敏感性。结果显示,相对于2009年的监测数据,2010—2012 年各地绿盲蝽种群对不同杀虫剂表现出不同程度的敏感性变化,但相对毒力比值均小于10倍。其中对毒死蜱、联苯菊酯的敏感性均未降低,菏泽种群表现为敏感性增强,相对毒力比值小于1。2011—2012年德州种群对丁硫克百威、灭多威和氟虫腈的敏感性降低,相对毒力比值大于3倍,其它种群敏感性变化不大,相对毒力比值均小于3倍。3年间菏泽种群对马拉硫磷的敏感性变化不大,相对毒力比值小于3倍,其它种群敏感性均有所降低。因此,毒死蜱、马拉硫磷、联苯菊酯、丁硫克百威等仍是山东棉区防治绿盲蝽的有效药剂。     

Cytochrome P450 monooxygenase-mediated permethrin resistance confers limited and larval specific cross-resistance in the southern house mosquito, Culex pipiens quinquefasciatus

The cytochrome P450-dependent monooxygenases (P450s) are an important enzymatic system that metabolizes xenobiotics (e.g., pesticides), as well as endogenous compounds (e.g., hormones). P450-mediated metabolism can result in detoxification of insecticides such as pyrethroids, or can be involved in the bioactivation and detoxification of insecticides such as organophosphates. We isolated (from the JPAL strain) a permethrin resistant strain (ISOP450) of Culex pipiens quinquefasciatus, having 1300-fold permethrin resistance using standard backcrossing procedures. ISOP450 is highly related to the susceptible lab strain (SLAB) and the high resistance to permethrin is due solely to P450-mediated detoxification. This is the first time in mosquitoes that P450 monooxygenase involvement in pyrethroid resistance has been isolated and studied without the confounding effects of kdr. Resistance in ISOP450 is incompletely dominant (D = +0.3), autosomally linked, and monofactorally inherited. It is expressed in the larvae, but not in adults. Cross-resistance to pyrethroids lacking a 3-phenoxybenzyl moiety (tetramethrin, fenfluthrin, bioallethrin, and bifenthrin) ranged from 1.5- to 12-fold. ISOP450 had only limited (6.6- and 11-fold) cross-resistance to 3-phenoxybenzyl pyrethroids with an α-cyano group (cypermethrin and deltamethrin, respectively). Examination of cross-resistance patterns to organophosphate insecticides in ISOP450 showed an 8-fold resistance to fenitrothion, while low, but significant, levels of negative cross-resistance were found for malathion (RR = 0.84), temephos (RR = 0.73), and methyl-parathion (RR = 0.55). The importance and uniqueness of this P450 mechanism in insecticide resistance is discussed.     

Effects of trichlorfon and sodium dodecyl sulphate on antioxidant defense system and acetylcholinesterase of Tilapia nilotica in vitro

The effects of organophosphorus insecticide trichlorfon, surfactant sodium dodecyl sulphate (SDS), and the mixture of trichlorfon and SDS on the antioxidant defense system and acetylcholinesterase (AChE) in Tilapia nilotica were assessed in vitro. Various concentrations of trichlorfon (0, 0.0001, 0.001, 0.01, 0.1 and 1 g/L) and SDS (0, 0.0625, 0.125, 0.25, 0.5, 1 g/L) were incubated with homogenate of liver and muscle, respectively, at 25 °C for 0, 30, 60 and 90 min. Two concentrations of mixture of trichlorfon and SDS (0.0001 g/L trichlorfon + 0.5 g/L SDS, 0.1 g/L trichlorfon + 0.5 g/L SDS) and 0.0001 g/L trichlorfon, 0.1 g/L trichlorfon, 0.5 g/L SDS and control, were incubated simultaneously with homogenate of liver and muscle, respectively, at 25 °C for 60 min. After incubation, the content of reduced-glutathione (GSH) and the activity of superoxide dismutase (SOD), catalase (CAT) and glutathione S-transferase (GST) in homogenate of liver were determined, and the activities of AChE in homogenate of muscle were also measured.Treatment with trichlorfon caused a significant concentration-dependent and time-related inhibition of AChE activity at all treatment concentrations and times since trichlorfon is a cholinesterase inhibitor. For the same trichlorfon treatment, an apparent decrease in GSH content was found in concentration of 0.01, 0.1, 1 g/L, whereas no significant alteration in antioxidant enzyme activity were found at all experiment concentrations and times, which might indicate that antioxidant enzymes have not involved in the metabolism of trichlorfon. The depletion of GSH might indicate that ROS could be involved in the toxic effects of trichlorfon. Exposure of SDS can inhibit activities of AChE, GST and CAT at concentrations of 0.5 and/or 1 g/L, which could be due to the denaturing process of SDS to the enzymes. For the mixture exposure of trichlorfon and SDS, the effect of the mixture of 0.0001 g/L trichlorfon and 0.5 g/L SDS on inhibition of AChE shows synergistic other than simple additive of trichlorfon and SDS. The combined effects of chemicals and detergents deserve to be particularly noted. It should be noted that the toxicity experiments were made in tissue homogenates instead of whole organisms. The responses against the toxic compounds will not be the same in both systems.     

Influence of pesticides and application methods on pest and predatory arthropods associated with cotton

Incidence of sucking pests was studied in a transgenic (Bt) and non-transgenic cotton (non-Bt) agro ecosystem in 2008 and 2009. Simultaneously, the influence of different pesticides applied in two different methods on sucking pests and generalist predators was investigated on transgenic cotton. In stem application, the insecticides solutions prepared were painted directly on the middle portion of the plant stem but in foliar application the recommended dosages of the insecticides were sprayed on the cotton plant. The transgenic and non-transgenic cotton did not differ significantly in the population of sucking pests. The different pesticides when applied by foliar sprays reduced significantly more sucking pests than stem application. Among the different insecticides used, imidacloprid caused the maximum reduction of the leaf hopper population, acetamiprid caused the maximum whitefly reduction, and clothianidin caused the maximum thrips reduction under foliar application. Via stem application, acetamiprid and thiomethoxam were found better in suppression of the sucking pests?? population, but the population of predators was significantly less disrupted by the stem application method. The foliar application was in general more effective; stem application may be more applicable early in the season when its efficacy was higher and when foliar sprays were particularly destructive to beneficial pests. In foliar application, all the systemic neonicotinoids like imidacloprid, clothianidin, admire, thiamethoxam and acetamiprid were found highly toxic to natural enemies in comparison with spirotetramat, buprofezin and fipronil.     

Thiamethoxam is a neonicotinoid precursor converted to clothianidin in insects and plants

Neonicotinoid insecticides are compounds acting agonistically on insect nicotinic acetylcholine receptors (nAChR). They are especially active on hemipteran pest species such as aphids, whiteflies, and planthoppers, but also commercialized to control many coleopteran and some lepidopteran pest species. The most prominent member of this class of insecticides is imidacloprid. All neonicotinoid insecticides bind with high affinity (I₅₀-values around 1 nM) to [³H]imidacloprid binding sites on insect nAChRs. One notable ommission is the neonicotinoid thiamethoxam, showing binding affinities up to 10,000-fold less potent than the others, using housefly head membrane preparations. Electrophysiological whole cell voltage clamp studies using neurons isolated from Heliothis virescens ventral nerve cord showed no response to thiamethoxam when applied at concentrations of 0.3 mM, although the symptomology of poisoning in orally and topically treated noctuid larvae suggested strong neurotoxicity. Other neonicotinoids, such as clothianidin, exhibited high activity as agonists on isolated neurons at concentrations as low as 30 nM. There was no obvious correlation between biological efficacy of thiamethoxam against aphids and lepidopterans and receptor affinity in electrophysiological and binding assays. Pharmacokinetic studies using an LC-MS/MS approach to analyze haemolymph samples taken from lepidopteran larvae revealed that thiamethoxam orally applied to 5th instar Spodoptera frugiperda larvae was rapidly metabolized to clothianidin, an open-chain neonicotinoid. Clothianidin shows high affinity to nAChRs in both binding assays and whole cell voltage clamp studies. When applied to cotton plants, thiamethoxam was also quickly metabolized, with clothianidin being the predominant neonicotinoid in planta briefly after application, as indicated by LC-MS/MS analyses. Interestingly, the N-desmethylated derivative of thiamethoxam, N-desmethyl thiamethoxam, was not significantly produced in either lepidopteran larvae or in cotton plants, although it was often mentioned as a possible metabolite, being nearly as active as imidacloprid. In conclusion, our investigations show that thiamethoxam is likely to be a neonicotinoid precursor for clothianidin.     

八种杀虫剂对黑粪蚊的防治效果及残留分析

选择8种杀虫剂,分别在实验室和菇房条件下研究其对黑粪蚊的防治效果和对平菇菌丝生长的影响,并分析施药后不同时间平菇中的农药残留.结果表明,40%辛硫磷EC、40%氧乐果EC、48%毒死蜱EC对黑粪蚊具有很好的防治效果,但对平菇菌丝的抑制率明显高于其它药剂;10%吡虫啉WP、4.5%高效氯氰菊酯EC不仅对黑粪蚊成、幼虫具有良好的防治效果,而且使用后对平菇菌丝生长的影响较小;2.5%高效氯氟氰菊酯EW、4.5%高效氯氰菊酯EC、1.8%阿维菌素EC等使用5天后均未检测到农药残留,5%氟虫腈SC和10%吡虫啉WP药后15天仍能检测到残留.     

The role of GABA and glutamate receptors in susceptibility and resistance to chloride channel blocker insecticides

Despite a point mutation in the pore-forming segment of the Rdl GABA receptor subunit that is widespread and persistent in insect populations and confers high levels of resistance to dieldrin and other polychlorocycloalkane (PCCA) insecticides, the phenylpyrazole insecticide fipronil, which binds at same site, has proven to be effective in controlling many insects, including dieldrin-resistant populations. Fipronil and its major sulfone metabolite are unique among chloride channel blocking insecticides in that they also potently block GluCls. We present here a patch clamp study of the action of fipronil sulfone on native GABA receptors and GluCl receptors from susceptible and dieldrin-resistant German cockroaches, to provide a better understanding of the effect of the Rdl mutation on the function and insecticide sensitivity of these two targets, and its role in resistance. Dieldrin blocked GABA currents with an IC₅₀ of 3 nM in wild-type cockroaches, and 383 nM in resistant insects, yielding a resistance ratio of 128. Fipronil sulfone blocked GABA currents with an IC₅₀ of 0.8 nM in susceptible insects and 12.1 nM, or 15-fold higher, in resistant insects. While both GluClD (desensitizing) and GluClN (non-desensitizing) receptors were found in German cockroach neurons, GluClN receptors were rare and could not be included in this study. GluClD receptors from resistant insects had reduced sensitivity to glutamate and a lower rate of desensitization than those from susceptible insects, but their sensitivity to block by fipronil sulfone was not significantly changed, with an IC₅₀ of 38.5 ± 2.4 nM (n = 8) in the susceptible strain and 40.3 ± 1.0 nM (n = 7) in the resistant strain. Fipronil sulfone also slowed the decay time course of GluClD currents. These results suggest that GluClD receptors contain the Rdl subunit, but their sensitivity to fipronil sulfone is not altered in resistant insects.     

Degradation of bifenthrin,chlorpyrifos and imidacloprid in soil and bedding materials at termiticidal application rates

Organophosphorus, pyrethroid and chloronicotinyl insecticides have been used to control termites in building structures in recent years. We investigated the degradation behaviour of three insecticides (bifenthrin, chlorpyrifos and imidacloprid) at termiticidal application rates under standard laboratory conditions (25 °C, 60% field moisture capacity and darkness) for 24 months. The study was carried out on one soil and two bedding materials (sand-dolomite and quarry sand), which are commonly used under housing in Australia. Experiments were also conducted to examine the effect of soil moisture on the degradation of these insecticides. Insecticide residues in the samples collected at different days after application were measured by high performance liquid chromatography (HPLC). The rate of degradation of bifenthrin and imidacloprid insecticides was adequately described by a first-order kinetic model (r² = 0.93–0.97). However, chlorpyrifos degradation was biphasic, showing an initial faster degradation followed by a slower rate. Therefore, the degradation data during the slower phase only (after a two-month period) followed the first-order law (r² = 0.95). Soil moisture had little effect on degradation of imidacloprid and bifenthrin. Among the three insecticides, bifenthrin and imidacloprid were most stable and chlorpyrifos the least. Chlorpyrifos showed a major loss (75–90%) of residue during the 24 months incubation period. In the bedding materials, simultaneous accumulation of the primary metabolite of chlorpyrifos, TCP (3,5,6-trichloro-2-pyridinol) was observed. Hydrolysis appeared to have caused the observed rapid loss of chlorpyrifos, especially in the highly alkaline bedding materials (sand-dolomite and quarry sand). © 1999 Society of Chemical Industry     

稻田常用农药对四地区二化螟盘绒茧蜂雌成蜂的触杀毒性

为明确稻田常用农药对二化螟幼虫期优势寄生性天敌二化螟盘绒茧蜂Cotesia chilonis(Mat-sumura)的毒性,采用药膜法在室内测定了7种杀虫剂原药以及18种常用农药制剂对扬州、安吉、金华和乐清4个地区二化螟盘绒茧蜂雌成蜂的触杀毒性。结果表明,7种杀虫剂原药中氟虫腈、毒死蜱和三唑磷对该蜂毒性较高,杀虫单、吡虫啉和阿维菌素次之,氯虫苯甲酰胺则最低。12种杀虫剂制剂中20%氯虫苯甲酰胺悬浮剂和3种阿维菌素相关制剂对该蜂毒性相对较低,其余均具高毒性;4种杀菌剂中的异稻.三环唑对该蜂高毒,苯甲.丙环唑次之,井岗.蜡芽菌(井冈霉素)和盐酸吗啉胍.三氮唑核苷则毒性最低;2种除草剂中苄嘧.丙草胺毒性高于苄.二氯。此外,同一种药剂对不同地区雌蜂的毒性也有所不同。     

Effects of seed potato tuber treatment with imidacloprid on some soil and foliar insects in Croatia

The treatment of seed potato tubers by imidacloprid, as well as the standard granular insecticides applied in the furrow, did not, in four years of trials, sufficiently prevent damage from wireworms, noctuid larvae and mole crickets to potato tubers. The main reason for this failure is the spatial and temporal distance between the application of insecticides and the moment when their action is needed. On the other hand, the effects of imidacloprid applied as seed tuber treatment on the larvae of the Colorado potato beetle was very good: depending upon conditions, it lasted from at least 55, to 70 days at the most. It protected the foliage from any substantial damage from the entire first generation, and ensured high yields. Therefore a decision on seed tuber treatment with imidacloprid in Croatia should primarily depend upon the cost/benefit calculation based on damage expected from the CPB (or aphids), and not from soil insect pests.     

The toxicity of five insecticides to earthworms of the Pheretima group,using an artificial soil test

An artificial soil test was used to assess the toxicity of five insecticides, used for turfgrass pest management, to earthworms of the Pheretima group (Megascolecidae). The effects of cyfluthrin, carbaryl, chlorpyrifos, fipronil and imidacloprid on earthworm mortality, earthworm biomass and individual earthworm mass, were assessed. Carbaryl and chlorpyrifos had a significant greater effect on earthworm mortality than cyfluthrin, seven days after the application of the insecticides. No other significant earthworm mortality was found. None of the insecticides had a significant influence on earthworm biomass. Cyfluthrin initially reduced individual earthworm mass, but not biomass, more than the other insecticides. Carbaryl reduced biomass more than the other insecticides for all the assessments. Carbaryl, imidacloprid and cyfluthrin had a larger negative effect than the control, fipronil and chlorpyrifos on individual earthworm mass in the 14 and 21 day assessments. © 2000 Society of Chemical Industry