THE MOVEMENT OF PARAQUAT IN PLANTS

Summary. A qualitative study of the movement of the herbicide paraquat from droplets applied to leaves of tomato plants, using ¹⁴C-methyl-labelled and ¹⁴C-ring-labelled paraquat dichloride and di(methylsulphate), has shown that it moves in the xylem with the transpiration stream. The chemical is as well transported from young leaves as from mature ones, and will move through a steam-ringed petiole. The enhancement of the amount of paraquat transported from the treated leaves which occurs when treated plants are kept in darkness for a period following treatment and then exposed to light, is probably due to the greater movement into the xylem through undamaged tissue which can occur in the dark. Once the chemical has been absorbed into treated leaves, light-induced damage is required for significant movement through the rest of the plant to take place, but the damage then inhibits further entry of paraquat into the xylem. The movement of paraquat in broad bean and maize is essentially similar, though the enhancement of movement by a period of darkness after application is much less marked.
La migration du paraquat dans les plantes     

Tumours of Begonia and some other ornamentals,induced by Corynebacterium fascians

In 1975 many tumours were observed in plants ofBegonia Schwabenland grown in Aalsmeer. Submersion of the roots ofNicotiana megalosiphon seedlings in a homogenate of tumorous tissue, induced tumours after two weeks. Short periods of submergence yielded results similar to those obtained after longer periods. Tumour homogenates lost their infectivity after ten min at 50°C. Aphids transmitted the infectious agent.Treatment with propylene oxide did not inhibit infectivity completely. Filtration through a 450 nm filter removed the infectious agent.Tobacco tumor virus or a viroid could not be isolated. Cultures ofCorynebacterium fascians, isolated from tumours ofN. megalosiphon were highly infectious and induced tumours in healthyN. megalosiphon andBegonia. Tumorous tissue homogenates ofPelargonium zonale, Dahlia sp.,Gladiolus sp., andLilium sp. also caused tumours inN. megalosiphon, from whichC. fascians was isolated. It was not possible to produce tumours inN. megalosiphon with homogenates from roses with symptoms of bud proliferation.Samenvatting In 1975 werden vele tumoren waargenomen inBegonia Schwabenland op Aalsmeerse bedrijven (Fig. 1). De infectiositeit van tumorweefsel kon goed en snel worden vastgesteld door de wortels van zaailingen vanNicotiana megalosiphon in een homogenaat van tumorweefsel te dompelen. Tumoren ontstonden na twee weken, de eindbeoordeling geschiedde na een maand (Fig. 2). Ook verschillende andereNicotiana spp.,Melilotus officinalis (Fig. 3) enPisum odoratum (Fig. 4) werden aangetast.Bij de infectiositeitstoets gaven zeer korte dompeltijden even goede resultaten als langere (Tabel 1). Infectieus sap verloor zijn infectievermogen na 10 min verhitting bij 50°C. Bladluizen brachten de smetstof over. Propyleenoxide verminderde de infectiositeit wel, doch onderdrukte deze niet totaal. Bij filtratie door een 450 nm filter bleef het infectieuse agens op het filter achter. Het tumor-inducerende agens was ook aanwezig in die delen van planten met tumoren welke gezond leken en het ging voor een gering deel over met zaad (Tabel 2).Uit tumoren konden wij geen tabakstumorvirus of een viroïde isoleren. Culturen vanCorynebacterium fascians, geïsoleerd uit tumoren vanN. megalosiphon bleken zeer infectieus en veroorzaakten tumoren inN. megalosiphon enBegonia. Homogenaten van tumorweefsel vanPelargonium zonale, dahlia (Fig. 5), gladiool (Fig. 6) enLilium Mid Century Hybrid Enchantment (Fig. 7) veroorzaakten ook tumoren opN. megalosiphon, waaruitC. fascians werd geïsoleerd. Met sap van kroeskopzieke rozen konden wijN. megalosiphon niet besmetten.     

Determination and persistence of imazalil in post-harvest-treated apples during cold storage

A method to determine imazalil (allyl 1 -(2, 4-dichlorophenyl)-2-imidazol- 1-ylethyl ether) on apples using high performance liquid chromatography is described. After harvest, fruits were immersed in an aqueous suspension (1 g litre-1) and cold stored (0-2°C) at 85-90% r.h. Samples were taken monthly and imazalil was determined in the peel, outer pulp, inner pulp and on whole fruit. Residues were 3.8-4.9 mg imazalil kg-1 and decreased during storage. Most imazalil was found on the peel and amounts in the pulp decreased toward the core.     

Combining competition from Lolium perenne and an insect–fungus combination to control Rumex obtusifolius seedlings

Although adult Rumex obtusifolius are problematic weeds, their seedlings are poor competitors against Lolium perenne, particularly in established swards. We investigated the possibility of using this weakness to augment control of R. obtusifolius seedlings with combinations of Gastrophysa viridula (Coleoptera: Chrysomelidae) and the rust fungus Uromyces rumicis. Rumex obtusifolius seedlings were grown in competition with L. perenne sown at different rates and times after R. obtusifolius: they competed successfully with L. perenne when sown 21 days before the grass. Sowing both species at the same time resulted in a dominant grass sward, with R. obtusifolius becoming dominant when sown 42 days prior to L. perenne. Grass sowing rate had no effect on R. obtusifolius growth or biomass. A second experiment investigated how competition from L. perenne sown 21 days after R. obtusifolius combined with damage from G. viridula and/or U. rumicis (applied at either the 3–4‐ or 10–13‐leaf stage, or at both stages) affected the growth and final biomass of R. obtusifolius. Beetle grazing at the latter leaf stage was the only treatment that reduced R. obtusifolius biomass, although rust infection at the earlier application led to an increase in shoot and root weight. The results are discussed in terms of the potential for use of these agents in the field.     

Pathogenicity of the root-knot nematode Meloidogyne javanica on potato

Host–parasite relationships and pathogenicity of Meloidogyne javanica on potatoes (newly recorded from Malta) were studied under glasshouse and natural conditions. Potato cvs Cara and Spunta showed a typical susceptible reaction to M. javanica under natural and artificial infections, respectively. In potato tubers, M. javanica induced feeding sites that consisted of three to four hypertrophied giant cells per adult female. Infection of feeder roots by the nematode resulted in mature large galls which usually contained at least one mature female and egg mass. In both tubers and roots, feeding sites were characterized by giant cells containing granular cytoplasm and many hypertrophied nuclei. Cytoplasm in giant cells was aggregated alongside the thickened cell walls. Stelar tissues within galls appeared disorganized. The relationship between initial nematode population density ( P ) [0–64 eggs + second-stage juveniles (J2s) per cm³ soil] and growth of cv. Spunta potato seedlings was tested under glasshouse conditions. A Seinhorst model [ y = m  + (1 −  m ) z ^{( P − T )}] was fitted to fresh shoot weight and shoot height data of nematode-inoculated and control plants. Tolerance limits ( T ) for fresh shoot weight and shoot height of cv. Spunta plants infected with M. javanica were 0·50 and 0·64 eggs + J2s per cm³ soil, respectively. The m parameter in that model (i.e. the minimum possible y -values) for fresh shoot weight and shoot height were 0·60 and 0·20, respectively, at P  = 64 eggs + J2s per cm³ soil. Root galling was proportional to the initial nematode population density. Maximum nematode reproduction rate was 51·2 at a moderate initial population density ( P  = 4 eggs + J2s per cm³ soil).     

Note: Comparison of three laboratory methods to evaluate the pathogenicity and virulence of tenPseudomonas syringae pv.syringae strains on apple, pear, cherry and peach trees

The pathogenicity and virulence of ten GreekPseudomonas syringae pv.syringae strains from different hosts (citrus, pear, apple, peach and cherry) were evaluated using three different laboratory methods, which produced results in good agreement. All ten strains were virulent on apple, pear, cherry and peach trees. The extent of tissue colonized varied considerably among strains and cultivars. On excised shoots and twigs of apple and pear, strains BPI 176, BPI 203, PI 2 and PI 14 were the most virulent and strains BPI 689, BPI 992, BPI 4, BPI 20, PI 18 and PI 19 were the least virulent. On excised shoots and twigs of peach and cherry, strains BPI 176, BPI 203, PI 2, PI 14, PI 18 and PI 19 were the most virulent and strains BPI 4 and BPI 20 were the least virulent. Moderate virulence was evinced by strains BPI 689 and BPI 992. These pathogenicity assays are proposed as rapid and reproducible screening systems to evaluate the susceptibility of apple, pear, cherry and peach cultivars to this bacterial pathogen.     

The effect of carbon dioxide under pressure against eggs of Ephestia kuehniella Zeller and adults of Stegobium paniceum (L.) and Oryzaephilus surinamensis (L.)

The efficacy of an atmosphere with a high content of carbon dioxide under a pressure of 5 and 10 bar against young eggs of Ephestia kuehniella Zeller (Lep.: Pyralidae) and adults of Stegobium paniceum (L.) (Col.: Anobiidae) and Oryzaephilus surinamensis (L.) (Col.: Cucujidae) was investigated. At a pressure level of 10 bar, a 100% mortality in eggs of E. kuehniella was obtained after 4 hours. Complete control was not obtained with the adult beetles, except for a 2 hour-treatment at 10 bar with individuals of S. paniceum, which not were offered protection. It is demonstrated that when working with an atmosphere of carbon dioxide under pressure of 10 bar for 2 hours, even a slight protection from food material will influence the mortality. The reason for these findings are discussed.     

Relationships Between Tillage and Spatial Patterns of Heterodera glycines

ABSTRACT The dynamics of Heterodera glycines spatial patterns were studied under different tillage systems in two naturally infested soybean fields in Iowa from 1994 to 1997. At each location, there were four different tillage treatments (conventional tillage, reduced tillage, ridge tillage, and no tillage). Soil samples were taken from 98 contiguous quadrats (5.2 m(2)) per plot in the fall of 1994, before any tillage was performed, and in the spring of the following 3 years shortly after planting. Cysts were extracted from soil samples by elutriation and counted, and eggs were extracted from cysts and enumerated. Spatial patterns of H. glycines populations were characterized by geostatistical analysis and variance-to-mean (VM) ratios. Semivariance values were calculated for cyst and egg densities and semivariograms were constructed. In general, there was greater spatial dependence among cyst populations than egg populations. In one field with a strongly aggregated initial H. glycines population, tillage practices resulted in changes in spatial patterns of H. glycines populations, characterized by spherical-model semivariogram parameters (sill, nugget effect, and range of spatial dependence). These parameters indicated increasing aggregation over time in no tillage and ridge tillage treatments, but decreasing aggregation in reduced and conventional tillage treatments. There was an increase of 350% in sill values (maximum semivariance) for cyst populations after 3 years of no tillage, but in the conventional tillage treatment, sill values remained unchanged or decreased over time as tillage was implemented. Semivariograms for cyst and egg population densities revealed strong anisotropy (directional spatial dependence) along soybean rows, coincident with the direction of tillage practices. VM ratios for cyst counts increased each year in the no tillage and ridge tillage treatments, but decreased for 2 years in reduced tillage and conventional tillage treatments. Final VM ratios for cyst and egg counts were highest in the no tillage treatment. In a second field, with low initial aggregation of H. glycines populations, there was little measurable change in semivariogram parameters after 3 years of no tillage, but in the conventional tillage treatment, populations became less aggregated, as the range, sill, and the proportion of the sill explained by spatial dependence decreased for cyst population densities. Our results indicated that in soybean fields with initially aggregated populations of H. glycines, no tillage and ridge tillage systems promoted aggregation of the nematode population, whereas conventional and reduced tillage systems resulted in a less aggregated spatial pattern.     

Evaluation of PCR,IEF and ELISA techniques for the detection and identification of potato cyst nematodes from field soil samples in England and Wales

Effective management of potato cyst nematodes (PCNs) requires simple, rapid and accurate identification and quantification of field populations. Soil samples from a survey of 484 fields in potato rotations in England and Wales were used to compare the identification and quantification of PCNs using IEF, PCR, ELISA and bait plant tests. The cyst counts and bait plant test revealed that 64.3% of field samples contained PCNs. Bait plant tests increased the detection rate of PCNs in field samples by 4–6.4%. This means that some infestations are cryptic and would not normally be detected by standard counts. IEF, PCR and ELISA methods distinguished between Globodera rostochiensis and G pallida and were able to register mixed populations; however they were not in full agreement. All methods suggested that G pallida is the dominant species in the field samples tested. The PCR results indicated that 66% of field samples contained pure G pallida, 8% contained pure G rostochiensis and 26% contained mixtures of the two species. Estimates of the relative process times taken per sample in the PCR, IEF and ELISA techniques are given. © 2001 Society of Chemical Industry     

Characterization of cereal bare patch isolates of Rhizoctonia solani by random amplified polymorphic DNA analysis

RAPD-PCR was used to characterize isolates of Rhizoctonia solani from bare patches in cereal and pasture crops at two locations in Western Australia, Newdegate and Esperance. All of the isolates belonged to anastomosis group 8, pectic zymogram group 1-1 or 2. The pectic zymogram assignment could be confirmed by RAPD-PCR. There was no difference in RAPD-PCR pattern between highly virulent and weakly virulent isolates at Newdegate, or between isolates from different patches at Newdegate. The Newdegate isolates were identical to isolates from Esperance, and to isolates from various locations in South Australia.