Finite dose diffusion studies: II. Effect of concentration and pH on NAA penetration through isolated tomato fruit cuticles

The effects of NAA [2‐(1‐naphthyl)acetic acid] concentration and pH on penetration of NAA from aqueous droplets (5 µl) through isolated tomato (Lycopersicon esculentum) fruit cuticles were studied using a finite dose diffusion system. Penetration time‐courses were characterized by a lag phase, which generally extended beyond the time of droplet drying. Initially penetration rates increased, reached a maximum penetration rate, remained constant for several hours, and then decreased with time. Penetration approached a plateau within 120 h after droplet application. Increasing NAA concentration in the donor droplet increased NAA penetration in both the presence and absence of the citric acid buffer (20 mM , pH 3.2). Maximum rates of penetration and the total amount of NAA that penetrated at 120 h were both linearly related to the initial concentration of the donor droplet (ranging from 0.001 to 0.1 mM NAA). The apparent first‐order rate constants for the concentration dependence of NAA penetration rates were greater with buffer than without (0.94 × 10⁻⁸ vs 0.50 × 10⁻⁸ m s⁻¹, respectively). While pH of the receiver solution (pH 6.2 vs 2.2) did not affect penetration, decreasing donor pH from 6.2 to 2.2 increased NAA penetration at 120 h. © 2000 Society of Chemical Industry     

Mobilities of Organic Compounds in Reconstituted Cuticular Wax of Barley Leaves: Effects of Monodisperse Alcohol Ethoxylates on Diffusion of Pentachlorophenol and Tetracosanoic Acid

Effects of monodisperse alcohol ethoxylates on mobilities of ¹⁴C-labelled pentachlorophenol (PCP) and tetracosanoic acid (C₂₄AC) in reconstituted cuticular wax of barley leaves were measured. Depending on the respective alcohol ethoxylate investigated, the diffusion coefficient (D) of PCP in barley wax was increased by factors ranging from 3·3 to 19·6, whereas D of C₂₄AC, was increased by factors varying between 22 and 315. In order to analyse the relationship between the concentration of surfactants in the wax and their effects on D, the amounts of alcohol ethoxylates dissolved in the wax at equilibrium with external concentrations well above the critical micelle concentration (CMC) were determined. Wax/water partition coefficients (K_ww) of the alcohol ethoxylates were about one order of magnitude lower than cuticle/water partition coefficients (K_cw), which is a consequence of the semi-crystalline structure of the wax compared with amorphous cutin. Correlations between effects on D and maximum amounts of alcohol ethoxylates dissolved in the wax were obtained indicating an unspecific wax/surfactant interaction. This was solely dependent on the amount of surfactant sorbed to the wax, leading to increased mobilities of pesticides in the wax. Applying ESR-spectroscopy, which gave an insight into the molecular structure of the wax, supported this interpretation of an unspecific plasticising effect of the alcohol ethoxylates on the molecular structure of the wax. The results obtained in this study are in good accordance with the results obtained in a recent study investigating the effects of the same group of alcohol ethoxylates on mobilities of pesticides in isolated, but intact, cuticular membranes of Citrus. This demonstrates that the investigation of isolated and subsequently reconstituted cuticular wax is a useful model system analysing the mechanisms of the surfactant interaction with the transport-limiting barrier of plant cuticles.     

A mechanistic analysis of penetration of glyphosate salts across astomatous cuticular membranes

Penetration of glyphosate salts across isolated poplar (Populus canescens (Aiton) Sm) cuticular membranes (CM) was studied using Na+, K+, NH4+, trimethylsulfonium+ (TMS) and isopropylamine+ (IPA) as cations. After droplet drying, humidity over the salt residues on the outer surfaces of the CM was kept constant, and cuticular penetration was monitored by sampling the receiver solution facing the inner surfaces of the CM. Glyphosate salts disappeared exponentially with time from the surfaces of the CM. This first-order process could be quantitatively described using rate constants (k) or half-times (time for 50% penetration; t1/2). Humidity strongly affected the velocity of penetration, as k increased by factors of 5.3 (K-glyphosate), 6.9 (TMS-glyphosate), 7.1 (NH4-glyphosate), 8.5 (Na-glyphosate) and 10.5 (IPA-glyphosate) when humidity was increased from 70 to 100%. Depending on the type of cation and humidity, t1/2 varied between 4 and 70h, but the humidity effect was statistically significant only at 100% humidity, when half-times were highest with IPA-glyphosate and lowest with TMS-glyphosate. Glyphosate acid penetration was measured only at 90% humidity and found to be extremely slow (t1/2 = 866 h). Adding 0.2 g litre-1 of a wetter (alkylpolyglucoside) to the donor increased IPA-glyphosate rate constants by about four times, but increasing concentration produced no further increase in k. When donors contained 0.2 g litre-1 wetter, further additions of 4 g litre-1 Ethomeen T25 did not change rate constants measured with IPA-glyphosate at 90% humidity, while Genapol C-100 and diethyl suberate increased k by only 35%. Concentration of IPA-glyphosate (1, 2 and 4 g litre-1) did not influence k at 90% humidity, and pH of donor solutions (4.0, 7.7, 9.5) had no effect on k of K-glyphosate at 90% humidity. Temperature (10 to 25 degrees C) had only a small influence on velocity of penetration of IPA-glyphosate and K-glyphosate, as energies of activation amounted to only 4.26 and 2.92 kJ mole-1, respectively. These results are interpreted as evidence for penetration of glyphosate salts in aqueous pores.     

Polydisperse ethoxylated fatty alcohol surfactants as accelerators of cuticular penetration. 2: Separation of effects on driving force and mobility and reversibility of surfactant action

Polydisperse ethoxylated fatty alcohol (EFA) surfactants can improve the performance of crop protection agents. At the cuticular level they act as accelerators of penetration by increasing the mobility of active ingredients in the cuticle, the barrier properties of which are mainly caused by cuticular waxes. Polydisperse Genapol C-050 (GP C-050, average formula C12.5E5.8) was also found to increase mobility in wax-extracted polymer matrix membranes (MX) of bitter orange and pear, indicating that sorption of surfactants increased segmental mobility of polymethylene chains in cutin and wax. Sorption into MX of the active fraction of GP C-050 from 5g litre⁻¹ micellar solutions was in equilibrium in less than 1 h after establishing contact. This is almost 100-fold faster than with cuticular membranes (CM). Temperature dependence of solute mobilities in CM was studied in order to measure activation energies (E_D) of diffusion in the presence and absence of aqueous surfactant solutions. Monodisperse fatty alcohol ethoxylates C8E3, C8E4 and C12E6, and (non-surface-active) tributylphosphate decreased E_D of the model compounds WL 110547 and bifenox in Citrus, Pyrus and Stephanotis CM by more than 100 kJ mol⁻¹. This corresponds to 50 to 275-fold increases of mobilities at 15 °C. Our data suggest that the decrease in activation energies with the concomitant accelerating effect on mobility contributes considerably to the effects of so-called activator surfactants. High temperature and accelerators act similarly on barrier properties of CM. It is shown that effects of both monodisperse and polydisperse EFA surfactants on solute mobility are reversible and that radiolabelled C12E8 penetrated pear CM rapidly. However, rates of penetration were lowered by excess amounts of WL 110547 and especially phenylurea. Partition coefficients of seven organic solutes between Capsicum fruit cuticles and GP C-050 were very low and, with the exception of methylglucose, smaller than 1. They decreased with lipophilicity and differed about 100-fold. Especially for the lipophilic compounds they were orders of magnitude lower than octanol/water or cuticle/water partition coefficients, which indicates the limited usefulness of these values for an understanding of penetration of active ingredients from formulation residues. © 1999 Society of Chemical Industry     

Visualization of the effect of a surfactant on the uptake of xenobiotics into plant foliage by confocal laser scanning microscopy

A radiolabelling method is generally used to determine the foliar uptake of xenobiotics. This technique cannot provide any information on the localization of chemicals inside leaf tissues. The influence of an alcohol ethoxylate surfactant on the uptake of three fluorescent dyes, difluorofluorescein (hydrophilic), rhodamine B (moderately lipophilic) and a naphthalimide dye (lipophilic), into the leaves of three contrasting species, bean (Vicia faba), wheat (Triticum aestivum) and cabbage (Brassica oleracea), at 16 h after treatment was measured using a conventional wash‐off method and also visualized in vivo by confocal laser scanning microscopy (CLSM). Whereas the lipophilic dyes showed greater intrinsic uptake than the hydrophilic one, the enhancing effect of the surfactant on uptake was more pronounced for the latter. CLSM revealed that the presence of the surfactant increased the transport of difluorofluorescein into the epidermal cells of bean and wheat leaves, but not cabbage leaves. Rhodamine B showed greatest transcuticular diffusion in all three species, but most of the dye moved into the vacuole of the epidermal cells. The naphthalimide dye was strongly retained by the wax–cuticle layer of all species, even in the presence of the surfactant. CLSM has proven to be an attractive tool for studying xenobiotic diffusion. The results obtained using fluorescent dyes are believed to be applicable to the foliar uptake of herbicides.     

Absorption, translocation and allocation of glyphosate in resistant and susceptible Chilean biotypes of Lolium multiflorum

Glyphosate [N-(phosphonomethyl) glycine] is currently the most important non-selective, wide-spectrum herbicide used worldwide. Introduced in 1974, glyphosate was initially a non-crop herbicide and plantation crop herbicide, although it is now widely used in no-till crop production and, more recently, for weed control in herbicide-resistant transgenic crops, such as maize, soybean and cotton ( Baylis 2000 ; Caseley & Copping 2000 ). Despite its widespread and long-term use, no case of evolved resistance to glyphosate was documented until 1996 ( Pratley et al . 1996 ). Since then, a few other cases have been reported. To date, evolved resistance to glyphosate has been identified and documented in Lollium rigidum in Australia ( Powles et al . 1998 ; Pratley et al . 1999 ), Eleusine indica in Malaysia ( Lee & Ngim 2000 ), and L. rigidum in South Africa and California (USA), and Conyzia canadensis in Delawere (USA) ( Van Gessel 2001 ). Also, accessions of L. rigidum from South Africa and California have been reported to resist glyphosate ( Heap 2001 ). In Chile, the first case of glyphosate-resistance in Lolium multiflorum was reported in 1999 and documented in 2003 ( Pérez & Kogan 2003 ). This case was the result of an intensive selection pressure caused by the continuous applications of glyphosate in fruit orchards over 8–10 years. The present study is a first approach to elucidating the mechanism involved in the resistance of one biotype of L. multiflorum selected in Chilean orchards.     

Effect of additives in aqueous formulation on the foliar uptake of dimethomorph by cucumbers

BACKGROUND: The efficacy enhancement of dimethomorph formulation by several adjuvants is thought to be through increased foliar uptake. In order to identify the most effective adjuvants, the adjuvancy of 36 additives was examined in aqueous formulations in relation to the absorption of dimethomorph by cucumber leaves. RESULTS: Polyethylene glycol monohexadecyl ethers with ethylene oxide (EO) contents of between 7 and 20, polyethylene glycol monooctadecyl ethers with EO contents of between 10 and 20 and polyethylene glycol monooctadecenyl ethers with EO contents of between 6 and 20 were effective adjuvants for promoting dimethomorph uptake from both aqueous acetone solutions and aqueous wettable powder (WP) suspensions into cucumber leaves. Polyethylene glycol monododecyl ethers with EO contents of between 7 and 9 were effective in promoting dimethomorph uptake from aqueous WP suspensions but less effective relative to the other adjuvants tested with aqueous acetone solutions. Foliar uptake of dimethomorph was also facilitated by the addition of methyl hexadecanoate, methyl octadecenoate and methyl octadecadienoate. CONCLUSIONS: Although the foliar uptake of dimethomorph from both aqueous WP suspensions and aqueous acetone solutions was greatest in the presence of fatty alcohol ethoxylates generally having a C₁₆ or C₁₈ lipophile, uptake from aqueous surfactant–acetone solutions was, on average, 7.6‐fold greater than that from aqueous WP suspensions containing surfactant. Copyright © 2009 Society of Chemical Industry     

Effects of temperature and concentration of the accelerators ethoxylated alcohols,diethyl suberate and tributyl phosphate on the mobility of [14C]2,4‐dichlorophenoxy butyric acid in plant cuticles

Intrinsic activities of monodisperse ethoxylated dodecanols (MEDs), diethyl suberate (DESU) and tributyl phosphate (TBP) were investigated using Stephanotis floribunda leaf cuticular membranes (CMs) and [¹⁴C]2,4‐dichlorophenoxy butyric acid (2,4‐DB) as a model solute. When sorbed in cuticular membranes, MEDs, DESU and TBP increase solute mobility and are called accelerators for this reason. With MEDs, dose‐effect curves (log mobility vs accelerator concentration) were linear but, with DESU and TBP, curves convex to the x axes were obtained that approached a maximum at 90 and 150 g kg⁻¹, respectively. Accelerators increased the mobility of 2,4‐DB in the CMs by 9‐ to 48‐fold, and effects were larger at lower temperatures (range 15–30 °C). Activation energy for diffusion of 2,4‐DB was 105 kJ mol⁻¹, decreasing with increasing accelerator concentrations to 26 kJ mol⁻¹ with DESU at 90 g kg⁻¹ and 64 kJ mol⁻¹ with TBP at 150 g kg⁻¹. Thus, the intrinsic activity of DESU was much higher than that of TBP, which implies that, for a given effect, less DESU than TBP would be needed. MEDs were also very effective accelerators, lowering activation energies to 36 kJ mol⁻¹. Data are discussed in relation to increasing rates of foliar penetration of active ingredients at low temperatures. © 2001 Society of Chemical Industry     

Finite dose diffusion studies: I. Characterizing cuticular penetration in a model system using NAA and isolated tomato fruit cuticles

A finite dose diffusion system was employed to study cuticular penetration of 2‐(1‐naphthyl) [1−¹⁴C]acetic acid (NAA) from simulated spray droplets through enzymatically isolated tomato fruit cuticles (Lycopersicon esculentum Mill cv Pik Red). Isolated cuticles were mounted on diffusion half‐cells with the cell wall surfaces facing a 20 mM citric acid receiver solution (pH 3.2, volume 2.9 ml, prepared with deionized water). A 5‐µl donor droplet containing NAA at 100 µM in 20 mM citric acid buffer (pH 3.2) was applied to the outer surface. Penetration was monitored by repeated sampling of the receiver solution. NAA penetration was characterized by (1) an initial lag phase of about 2.3 h, (2) a phase of nearly constant maximum rate of penetration averaging 6.3% of applied NAA h⁻¹ (equivalent to 0.032 nmol h⁻¹) and (3) a plateau phase approaching an asymptote at 81.2% of applied NAA (equivalent to 0.406 nmol) at 120 h. Within 1 h after application droplets appeared dry on visual inspection. Immediately after droplet drying, 7.0% of the applied NAA was sorbed to the cuticle, but only 0.5% penetrated into the receiver solution, indicating that penetration occurred almost exclusively from the apparently dry deposit. At 120 h, 5.2% of the NAA applied was associated with the deposit and 4.3% with the cuticle. The distribution of maximum rates of penetration was log‐normal, but penetration at 120 h followed a normal distribution. Cuticle thickness (estimated 5–25 µm) had no significant effect on NAA penetration. Maximum rates of penetration through pepper fruit and citrus and ficus leaf cuticles were 4.9‐, 2.6‐ and 0.1‐times that through tomato fruit cuticles. At 120 h, penetration averaged 85.5, 79.5 and 34.7% for pepper, citrus and ficus cuticles, respectively. Extracting epicuticular and embedded waxes increased NAA penetration rates through tomato fruit cuticle more than three‐fold, but had little effect on penetration at 120 h (71.0 vs 87.7% for cuticular vs dewaxed cuticular membranes). The maximum penetration rate and total penetration were found to be useful parameters in describing the penetration time‐course. © 2000 Society of Chemical Industry     

两种喷雾助剂对氟磺胺草醚在反枝苋上的吸收和药效的影响

采用14C-氟磺胺草醚同位素标记法研究了喷雾助剂JFC 和ABS(十二烷基苯磺酸钠)对14C-氟磺胺草醚在反枝苋上的吸收和药效的影响。结果表明,在药液中添加2 g/L的JFC ,反枝苋对14C-氟磺胺草醚的吸收面积可增加1.4倍,吸收量增加3.2倍,药效提高28.5%;添加2 g/L的ABS ,反枝苋对14C-氟磺胺草醚的吸收面积增加1.3倍,吸收量增加1.0倍,药效提高19.2%。JFC不但具有促进药液在反枝苋叶面扩展的能力,还具有促进药剂渗透的能力,当添加2 g/L的JFC 时,反枝苋单位面积吸收强度增加75.7%;ABS基本上不能增加反枝苋单位面积的吸收强度,只具有促进药液扩展的能力。     

Finite dose diffusion studies: III. Effects of temperature, humidity and deposit manipulation on NAA penetration through isolated tomato fruit cuticles

Effects of temperature, humidity, rewetting and removal of deposits on penetration of NAA [2-(1-naphthyl)acetic acid] through isolated tomato (Lycopersicon esculentum Mill) fruit cuticles were studied using a finite dose diffusion system. In this system, an aqueous 5-microliter droplet (0.1 mM NAA in 20 mM citric acid buffer) is applied to the outer surface of a cuticle, which is mounted in a glass diffusion half-cell. The cell wall surface is in contact with a receiver solution (20 mM citrate). Penetration is monitored by repeated sampling of the receiver solution. Droplets appeared dry on visual inspection within 1 h of application, but significant NAA penetration continued after droplet drying. Maximum rates of NAA penetration increased exponentially as temperature was increased (from 5 degrees to 35 degrees C), the energy of activation averaging 153 (+/- 11.6)kJ mol-1. At 35 degrees C, penetration reached a plateau within 10 h of application (at 91.1 (+/- 1.0)% of dose applied) while at 5 degrees C penetration after 800 h reached only 30.2 (+/- 7.5)%. Increasing relative humidity from 20 to 80% increased maximum rates [from 1.0 (+/- 0.21) to 2.7 (+/- 0.80)% h-1] and penetration at 120 h after application [from 36.8 (+/- 2.1) to 64.3 (+/- 3.7)%]. Rewetting deposits at 120, 240 and 360 h after application resulted in increased NAA penetration. However, amounts and rates of NAA penetration progressively decreased with each subsequent rewetting. Removal of deposits by cellulose acetate stripping at various times after droplet application resulted in a rapid decrease in NAA penetration. NAA penetration following deposit removal was always less than 6.1% of the amount of NAA applied and averaged 0.5 (+/- 0.2)% when deposits were removed immediately after droplet drying.     

Sorption in reconstituted waxes of homologous series of alcohol ethoxylates and n-alkyl esters and their effects on the mobility of 2,4-dichlorophenoxybutyric acid

Equilibrium sorption of n-alkyl esters (dimethyl suberate, diethyl suberate, diethyl sebacate, dibutyl suberate and dibutyl sebacate) and monodisperse alcohol ethoxylates (diethylene glycol, tetraethylene glycol, pentaethylene glycol, hexaethylene glycol and octaethylene glycol monododecyl ether) between the reconstituted cuticular waxes of Stephanotis floribunda Brongn (Madagascar jasmine) or Hordeum vulgare L (barley) leaves and an external aqueous receptor solution was determined. Logarithms of the wax/receptor partition coefficient (K(wax/rec)) of the n-alkyl esters increased linearly with the number of C-atoms. With alcohol ethoxylates, log K(wax/rec) decreased linearly with the number of ethylene oxide units. For both groups of compounds, K(wax/rec) increased with increasing lipophilicity. The values of K(wax/rec) in Stephanotis wax were between 5 and 16 times higher than in barley wax. It is argued that this difference was due to different chemical composition and crystallinity of the waxes. Mobility of [14C]2,4-dichlorophenoxybutyric acid (2,4-DB) in reconstituted Stephanotis and barley wax was increased by a factor of 2-8 by both n-alkyl esters and alcohol ethoxylates. Effects on the mobility of 2,4-DB were linearly related to the internal concentrations of n-alkyl esters and alcohol ethoxylates in reconstituted Stephanotis or barley wax. At the same internal concentrations the effect of n-alkyl esters on the mobility of 2,4-DB in wax exceeded that of alcohol ethoxylates by between 1 and 2 orders of magnitude. Results are discussed in relation to formulating systemic pesticides.     

Visualisation of the uptake of two model xenobiotics into bean leaves by confocal laser scanning microscopy: diffusion pathways and implication in phloem translocation

The diffusion of two fluorescent dyes, Oregon Green 488 (Oregon Green) and Rhodamine B into the leaves of broad bean (Vicia faba L) plants was studied to simulate the foliar uptake process of pesticides. The uptake rate of these model xenobiotics into bean foliage was measured using a standard leaf surface wash-off method. Diffusion into leaf tissues was visualised in vivo by confocal laser scanning microscopy (CLSM). The moderately lipophilic dye (Rhodamine B) showed faster uptake than the hydrophilic one (Oregon Green), despite the former being a larger molecule. While no distinct channels or domains for preferential entry of any of the dyes could be detected in the cuticle layer by CLSM, two different diffusion patterns were identified for the movement of these two dyes after traversing the cuticle. Upon desorption from the cuticle, Rhodamine B diffused extensively into the vacuole of the epidermal cells. Further transport of this dye from the epidermal cells to the mesophyll cells was not observed. In contrast, Oregon Green was found in the epidermal cell walls and cytoplasm, and was also present in the mesophyll cells. Examination of the petioles of the treated leaves revealed that, once absorbed, Oregon Green moved readily out of the treated leaf, whereas Rhodamine B did not show any phloem translocation. It is proposed that these two different diffusion characters may be responsible for the contrasting phloem mobility of the two xenobiotics. The results are discussed in relation to the current knowledge on the uptake, translocation and efficacy of pesticides as influenced by their properties.     

Screening of weed extracts for antifungal properties against Colletotrichum lagenarium,the causal agent of anthracnose in cucumber

The antifungal activity of the leaf extracts from 203 weed species was investigated by performing a bioassay using cucumber plants and Colletotrichum orbiculare. The leaf extracts from four families, namely, Urticaceae, Onagraceae, Commelinaceae, and Solanaceae, showed a relatively stronger inhibition of the anthracnose lesions in cucumber plants when compared with the other families investigated in the study. A remarkable inhibition of anthracnose infection in cucumber leaves was observed with the extracts from the following 19 weed species: Boehmeria nipononivea and Boehmeria longispica, Persicaria scabra, Ranunculus japonicus and Ranunculus sceleratus, Cardamine flexuosa, Oenothera biennis, Aeschynomene indica, Indigofera pseudo‐tinctoria, Torilis scabra, Calystegia japonica, Solanum americanum, Bidens pilosa, Gnaphalium japonicum, Kalimeris yomena, Bromus catharticus, Cynodon dactylon, Alopecurus aequalis, and Scirpus tabernaemontani. In particular, it is noteworthy that the extracts from C. dactylon, K. yomena, and S. americanum completely inhibited anthracnose infection in cucumber.     

三种叶面肥在新疆两种葡萄上应用效果的比较研究

研究了3种叶面肥对红地球葡萄和木纳格葡萄产量和品质的影响。结果表明,在葡萄不同生育时期喷施螯合氨基酸钙液肥、腐植酸液肥和平衡营养肥,均明显增加了2个葡萄品种叶片叶绿素SPAD值、产量、可溶性固形物含量和还原型Vc含量,显著降低可滴定酸含量。其中红地球葡萄和木纳格葡萄,以连续喷施4次螯合氨基酸钙液肥效果最好:每公顷产量增幅分别为8.50%和17.15%,明显高于其它两喷肥处理,品质也好于其它两喷肥处理。     

Dieback and mortality of Nothofagus in Britain: ecology,pathogenicity and sporulation potential of the causal agent Phytophthora pseudosyringae

Since 2009 extensive dieback and mortality of Nothofagus obliqua, associated with bleeding cankers on stems and branches, has been observed in the UK. The causal agent was identified as Phytophthora pseudosyringae, based on morphological and analysis of the internal transcribed spacer (ITS) sequences. Between 2011 and 2013, a survey assessed the frequency and nature of these P. pseudosyringae infections. Mature trees of Nothofagus with stem lesions caused by P. pseudosyringae were found across England, Scotland and Wales. Additional symptoms such as twig blight and leaf necrosis indicated that aerial infection was occurring. Besides N. obliqua, other hosts regularly encountered included Nothofagus alpina, Fagus sylvatica and Vaccinium myrtillus. In pathogenicity tests involving inoculation of logs, P. pseudosyringae was shown to be an aggressive bark pathogen of N. obliqua and F. sylvatica, but significantly less aggressive on N. alpina. Foliage susceptibility and sporulation tests showed marked differences between the six host species tested. Leaves of N. obliqua and V. myrtillus were highly susceptible. Leaves of N. alpina were moderately susceptible, those of Rhododendron ponticum slightly susceptible and those of F. sylvatica not susceptible at all. High levels of sporulation were observed only on inoculated N. obliqua and V. myrtillus leaves. This suggests that P. pseudosyringae may sporulate heavily on N. obliqua foliage in the field and that this inoculum initiates the aerial lesions observed on the shoots, branches and stems. The results also suggest that P. pseudosyringae has the potential to pose a serious threat to N. obliqua and other Nothofagus species in their Southern Hemisphere native ranges.     

Mobility of oxathiapiprolin in and between tomato plants

BACKGROUND

Oxathiapiprolin (OXPT; FRAC code 49) is a new piperidinyl-thiazole isooxazoline anti-oomycete fungicide that targets oxysterol-binding proteins. The fungicide is known to translocate acropetally from root to shoot to protect plants against fungal attack.

RESULTS

OXPT is ambimobile. It can also translocate basipetally from shoot to root. OXPT exhibits an unprecedented capacity for trans-plant protection. When two tomato plants are grown in one pot, and one is treated with OXPT (on the stem, leaves or apex), while the other plant and soil surface are adequately covered, both plants become protected against late blight caused by Phytophthora infestans.

CONCLUSION

Trans-plant systemic protection induced by OXPT involves translocation of the fungicide from the shoot of the treated plant to its root, exudation into the soil and uptake by the root of the neighboring untreated plant to protect it against the disease. Liquid chromatography–tandem mass spectrometry analyses confirmed the occurrence of OXPT in root exudates of OXPT-treated tomato plants in quantities sufficient to protect detached tomato leaves and intact plants against P. infestans. © 2022 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.