Distribution of glyphosate and of its target enzyme inside wheat plants

Enolpyruvylshikimate phosphate (EPSP) synthase activity has been measured in different organs of 1–14-day-old wheat seedlings growing in culture chambers. Enzyme activity was first detected after two days, and reached its maximum value at day 4. It remained almost unchanged for 14 days thereafter. During germination, one of the most important sources of enzyme was the seed scutellum. Later, the developed leaves contained 43% of the whole stock of enzyme. Although the enzyme distribution was not identical under light or in the dark, there was no evident light induction of EPSP synthase. High enzyme activity was found in the coleoptile, continuing for the whole life-time of this organ, and which might be associated with its lignification. Five to 40% of the total enzyme was found in the roots, reaching a maximum at 14 days. At this stage, glyphosate applied to the first grown leaf was phloem-transported to the sink organs, with no clear relationship being shown between EPSP synthase activity and herbicide quantity in each organ. At day 4, glyphosate treatment, by soaking the seedlings in the herbicide solution, was followed by an active phloem transport from the scutellum to the growing parts. The average internal concentration of radiolabelled compounds (glyphosate plus its possible derivatives) which induced wheat seedling growth decrease, was shown to reach 50 to 100 μM under our conditions.     

Some ecological and behavioural aspects of siganid populations in the Red Sea and Mediterranean coasts of Israel in relation to their suitability for aquaculture

A comparative study of five populations of fishes: Siganus rivulatus (Forskal) and Siganus luridus (Ruppell) from both the Red Sea and Mediterranean Sea and Siganus argenteus (Quoy and Gaimard) from the Red Sea was carried out during 1972. The study included ecological and behavioural aspects that may have significance in determination of suitability of the species for aquaculture. Emphasis has been put on the behaviour, reproduction, availability of fry and resistance to changes in salinity levels.     

Effect of endotoxic compounds isolated fromVerticillium lecanii on the sweetpotato whitefly,Bemisia tabaci

Toxic products extracted by methanol from intact mycelia ofVerticillium lecanii were tested for their toxicity to eggs, larvae, pupae and adults ofBemisia tabaci and additional insects. All stages ofB. tabaci were sensitive to the toxin, with larvae showing the highest, and adults the lowest, sensitivity. Using a 0.5% crude toxin preparation, the mortality rate ofB. tabaci was 88%, 53.5%, 53.2% and 37% for larvae, eggs, pupae and adults, respectively. High sensitivity of adults, which was characterized by rapid paralysis followed by death, was observed inB. tabaci, Myzus persicae, Aphis gossypii, Acyrthosiphon pisum andFrankliniella occidentalis. Other insects,viz., Heliothis peltigera, Maladera matrida, Carpophilus hemipterus andCeratitis capitata, exhibited significantly lower sensitivity. The toxin was partially purified by differential extraction with organic solvents and on silica gel H and Sephadex LH 20 columns. Based on the toxin inactivation by saponification and its mobility in a polar solvent on thin layer chromatography, it is suggested that the toxic products might be phospholipids.     

Kinetics of Uptake and Metabolism of Atrazine in Model Plant Systems

The present work concerns atrazine absorption and metabolism by corn (Zea mays.) seedlings immersed in an aqueous medium in comparison with Acer pseudoplatanus cell cultures. At the point of equilibrium, the apparent concentration inside the A. pseudoplatanus cells (with a moderate lipid content: 0·17% of dry weight) was about twice that of the medium. This equilibrium was probably due to a simple partition process; part of the atrazine was dissolved in the cell water and reached the same concentration as in the external medium while the rest was concentrated inside the cellular lipids. The theoretical calculation of the lipid/water partition, taking into account the value of log P measured not with the lipids but with octanol (log P=2·5), gave a value of 1·5 for concentration inside the plant material. Such an equilibrium, resulting from a partition process between water and lipids, was also obtained in non-living corn seedlings. In living seedlings, an over-concentration of radioactivity due to [¹⁴C]atrazine derivatives was rapidly obtained inside roots and shoots giving concentrations respectively 7- and 12-fold higher than that of atrazine in the external medium. This was due to very rapid chemical transformation of atrazine into its hydroxy derivatives, especially hydroxyatrazine. This hydrolysis of atrazine in corn was due to the presence of high levels of benzoxazinone derivatives in corn seedling cells. The hydroxylated metabolites were able to concentrate in the cells very rapidly and were unable to diffuse freely into the external medium. As a consequence, this process facilitated the penetration of large quantities of atrazine which became rapidly hydroxylated, allowing therefore the passive penetration of atrazine to be further improved, since the concentration C₁ in the receiver compartment was always close to zero. The passive transfer of atrazine, following Fick's law: dq/dt=-Pa (C₀–C₁), was therefore optimized. © 1997 SCI.     

Construction of a genetic map of melon with molecular markers and horticultural traits, and localization of genes associated with ZYMV resistance

Abstract: A partial linkage map of melon was constructed from a cross between PI414723 and Dulce. Twenty-two SSR, 46RAPD, 2 ISSR markers and four horticultural markers [female flower form (a), Fusarium resistance, striped epicarp (st), and fruit flesh pH (pH)] were analyzed in an F₂/F₃ population to produce a map spanning 14 linkage groups. We report for the first time map positions for the st, a, and pH genes. One SSR marker was tightly linked to pH. Mapping the a gene for the female flower form to molecular linkage group 4 enabled the merging of the map of horticultural traits with the of molecular markers in this region. Using the 22 SSR markers of this map, two of the three postulated ZYMV resistance genes were located using a BC₁ population (PI414723 recurrent parent). One SSR marker was tightly linked to a ZYMV resistance gene, designated Zym-1. This revised version was published online in August 2006 with corrections to the Cover Date.     

Introduced <Emphasis Type="Italic">Tuber aestivum</Emphasis> replacing introduced <Emphasis Type="Italic">Tuber melanosporum</Emphasis>: a case study

A Tuber melanosporum plantation established in 1994/1995 on Kibbutz Bar’am (in the Upper Galilee, Israel) gradually lost its T. melanosporum mycorrhiza. In 1999, T. aestivum inoculated seedlings were inadvertently introduced into the plantation to fill the gaps between trees. A single T. melanosporum fruit body was found in 1999. Although no truffles were found after 1999 and until 2009, in that year and in 2010, truffles were collected. Morphological and molecular analyses proved these to be T. aestivum. Thus, the intentionally introduced T. melanosporum mycorrhiza was replaced by that of another introduced mycorrhizal fungus, T. aestivum. Local oak species produced higher yields compared to introduced host species known to be good T. melanosporum plant symbionts. The yield was comparable to that reported for young commercial orchards, but the fruiting season was earlier than in Europe.     

Contents Volume 127 2002

Volume Contents

Contents Volume 127 2002     

Estimation of between and within accession variation in selected Spanish melon germplasm using RAPD and SSR markers to assess strategies for large collection evaluation

The population structure of 15 Spanish melon (C. melo L.)accessions, mostly of Group Inodorus, was assessed by the analysis of 16individuals of each accession using 100 random amplified polymorphic DNA (RAPD) bands produced by 36 primers, and allelic variation at 12microsatellite (SSR) loci (23 alleles). A relatively high level of polymorphism (25.6%) was detected using RAPD markers, and eight SSR loci (66.7%) were useful in discriminating accessions. Cluster analysis using RAPD- and SSR-based genetic distance estimates resulted in similar and consistent groupings of most of the accessions studied. The mean genetic distance and standard error among accessions estimated by RAPD variation was 0.421 ± 0.099, and mean SSR-based genetic distance estimate was 0.285 ± 0.141. Albeit many dominant markers examined were fitted to a 3:1 test ratio, deviation from this ratio and from Hardy-Weinberg expectations for many SSR loci suggests that some populations were in genotypic disequilibrium. Moreover, a higher level of genetic variation was observed between Cassaba market classes than within accessions, suggesting that, depending upon the accession, allelic fixation has occurred in these populations. The relatively high level of heterogeneity observed (different band morphotypes and cluster grouping within a particular market class), however, indicates that the Spanish melons examined possess a relatively broad genetic background. An appraisal of accession population structure such as the one reported herein indicates that bulk sampling techniques coupled with molecular analysis techniques that employ a unique array of discriminating markers can provide information leading to effective strategies for diversity analyses of large collections. This revised version was published online in August 2006 with corrections to the Cover Date.     

Effects of bifenox and oxadiazon on isolated chloroplasts,plant mitochondria and leaf pieces

The effects of bifenox (methyl 5-(2,4-dichlorophenoxy)-2-nitrobenzoate) and oxadiazon (5-tert-butyl-3-(2,4-dichloro-5-isopropoxyphenyl)-1,3,4-oxadiazol-2(3H)-one on photosynthetic activity were investigated in isolated chloroplasts, and on respiratory activity in isolated mitochondria. The global effects of these chemicals were also investigated on cucumber cotyledon pieces. It was found that, in vitro, bifenox and oxadiazon acted on cotyledon pieces as typical diphenyl ether herbicides, causing complete pigment bleaching, even at low concentrations. In addition, bifenox and oxadiazon were shown to inhibit the photosynthesis process at the chloroplast level. At concentrations of up to 40-50 μM, oxadiazon and bifenox were observed to inhibit fully the light-dependent oxygen evolution of spinach class A chloroplasts, oxadiazon acting preferentially on electron transfer at the PS II level whereas bifenox acted on the photophosphorylation process. Comparison of the amounts of herbicide needed to inhibit photosynthesis and to cause bleaching of cucumber pieces leads to the conclusion that photosynthesis inhibition by bifenox and oxadiazon is only a secondary effect.