No abstract

Field experiments were conducted in the two cropping seasons between 2002 and 2004 to determine effects on soil-borne diseases, weeds and yield of strawberry of raised bed solarization (RBS), alone or with chicken manure (CM) amendment, methyl bromide (MB), TeloDrip (1,3-dichloropropene + chloropicrin), short RBS combined with reduced doses of metam sodium (MS) and TeloDrip. In both seasons, raised bed soil solarization (for 7 weeks) alone or with CM amendment (10 t/ha), MS (50 ml/m 2 ) after 2-week RBS, and MB (50 g/m 2 ) significantly reduced soil-borne diseases (caused by Rhizoctonia spp. and Phytophthora cactorum) while application of TeloDrip at a rate of 500 kg/ha and a half-dose after short solarization controlled the soil-borne diseases to a lesser extent in the 2003-2004 cropping season. All treatments provided effective control of four weed species; annual bluegrass (Poa annua), common purslane (Portulaca oleracea), redroot pigweed (Amaranthus retroflexus) and barnyardgrass (Echinochloa crus-galli) but not horseweed (Conyza canadensis). In the first year trial, total marketable yields from RBS with or without CM and 2-week solarization plus MS were equivalent to yields produced by MB treatment whereas only raised bed soil solarization and CM amendment led to the same increase of yield as MB in the second year.

Pseudomonas isolates from different crop plants were screened for in vitro growth inhibition of Phytophthora capsici and production of biosurfactant. Two in vivo experiments were performed to determine the efficacy of selected Pseudomonas strains against Phytophthora blight of pepper by comparing two fungicide treatments [acibenzolar-S-methyl (ASM) and ASM + mefenoxam]. Bacterial isolates were applied by soil drenching (1 × 109 cells/ml), ASM (0.1 μg a.i./ml) and ASM + mefenoxam (0.2 mg product/ml) were applied by foliar spraying, and P. capsici inoculum was incorporated into the pot soil three days after treatments. In the first experiment, four Pseudomonas strains resulted in significant reduction from 48.4 to 61.3% in Phytophthora blight severity. In the second experiment, bacterial treatments combining with olive oil (5 mL per plant) significantly enhanced biological control activity, resulting in a reduction of disease level ranging from 56.8 to 81.1%. ASM + mefenoxam was the most effective treatment while ASM alone was less effective in both bioassays. These results indicate that our Pseudomonas fluorescens strains (6L10, 6ba6 and 3ss9) that have biosurfactant-producing abilities are effective against P. capsici on pepper, and enhanced disease suppression could be achieved when they were used in combination with olive oil.

No abstract

The aim of this study was to determine the effect of soil solarization on soilborne diseases, weeds and plant yields by using polyethylene film (30-μm-thick) containing different additives [ultraviolet (UV), ultraviolet + infrared (UV + IR), ultraviolet + infrared + anti-fog + anti-dust (UV + IR + AF + AD)], and used polyethylene film (260-μm-thick). Trials were conducted in commercial strawberry (Fragaria ananassa cv. 'Camarosa') fields in the town of Sultanhisar in Aydin province, Turkey, between 2007 and 2009. The highest soil temperatures at the depth of 10 cm under a polyethylene sheet containing UV + IR + AF + AD were 54°C in 2007 and 50.7°C in 2008. During the 2007 growing season, collapse and death of strawberry plants were not detected. At the end of the 2008 season (May-June), collapsed and dying strawberry plants were observed. Pure cultures of Macrophomina phaseolina and Rhizoctonia solani were isolated from affected roots and crowns of plants. Viability studies of M.phaseolina were conducted under various field conditions and temperatures and M. phaseolina sclerotia survived more than 18 days at 45°C. There was a sharp decline in M. phaseolina at 50°C, where it survived for 19 h but was completely killed at 20 h. It first lost viability after 17 h at 50°C and after 60 min at 55°C. In the field, solarization did not reduce the viability of M. phaseolina at a soil depth of 10 or 20 cm; however, a significant reduction (66%) in survival was determined at a soil depth of 5 cm. All treatments controlled Portulaca oleracea, Amaranthus spp., Digitaria sanguinalis, Echinochloa crus-galli, Veronica hederifolia, Raphanus raphanistrum, Setaria verticillata and Mercurialis annua at a rate of 100%, but no treatment was effective on Cyperus rotundus. The marketable fruit yield was 38,004 kg.ha −1 for UV + IR, 35,834 kg.ha −1 for UV-added polyethylene film and 35,368 kg.ha −1 for used polyethylene sheetcovered plots, whereas it was 27,365 kg.ha −1 for untreated control plots.

With a typical Mediterranean climate, Aydin is the third largest strawberry-producing province, responsible for 13% of the overall strawberry production in Turkey. Strawberries (Fragaria × ananassa Duchesne) are mainly grown in raised, plastic-mulched beds under tunnels and soil solarization is the most effectively used management practice to control soil-borne pathogens. During October 2011 and 2012, 2 months after planting, wilting and collapse of plants were observed on commercial strawberry (cv. strawberry Festival) fields in Sultanhisar town of Aydin Province. Eleven percent of the plants were wilted and died. Symptomatic plants exhibited blackened necrotic discoloration of roots and in the cross section of crowns. A fungus was consistently isolated from pieces of infected tissue cut aseptically from the crowns and placed on potato dextrose agar. Fungus produced white colonies and later turned olivaecious black with dense aerial mycelium after 4 to 5 days incubation at 27°C. Dark brown to black pycnidia that formed on 20- to 30-day-old pure cultures under daylight conditions produced abundant conidia that were two-celled, thick-walled, and oval shaped with longitudinal striations. Single spore isolates from 12 samples were obtained and stored for further identification. The average size of 300 conidia was 25.42 ± 2.12 × 12.87 ± 1.08 μm. The morphology of the fungus was similar to Lasiodiplodia theobromae (Pat.) Griff. & Maubl. (syn. Botryodiplodia theobromae Pat.). To confirm the identity of the isolates, the internal transcribed spacer (ITS) region of ribosomal DNA and the elongation factor 1-alpha gene were amplified with the universal ITS1/ITS4 and EF1-688F/EF1-1251R (1) primers, respectively. The amplicons from 12 isolates were commercially sequenced at Macrogen (Korea) and were deposited in GenBank under consecutive accession numbers KF910369 to KF910380 and KJ641536 to KJ641547. Sequence comparison and phylogenetic analysis revealed that all 12 isolates were closely related and belonged to L. theobromae. Pathogenicity tests were performed by the toothpick technique (2) under greenhouse conditions (28°C, 14/10-h day/night, 70% RH) on potted strawberry plants (cv. strawberry Festival). Toothpicks carrying fungal growth taken from 1-week-old corn meal agar cultures of the tested isolates was placed into the basal crown tissue of the plants by piercing about 5 mm depth. Six plants were inoculated for each isolate and six were treated with sterile toothpick for control. All inoculated plants developed wilting and dieback symptoms resembling those of naturally infected plants within 2 to 3 weeks of incubation. All plants inoculated with the tested isolates collapsed after 4 weeks and showed discoloration of internal crown tissue. Control plants did not exhibit any disease symptoms, and crown tissue was symptomless. L. theobromae was successfully re-isolated from lesions of all inoculated plants. L. theobromae has been reported to cause cankers and dieback in a wide range of hosts in tropical and subtropical regions of the world (3). To the best of our knowledge, this is the first report of L. theobromae causing dieback on strawberry plants. References: (1) A. Alves et al. Fungal Divers. 28:1, 2008. (2) M. E. A. El-Morsi and I. A. Ibrahim. Wudpecker J. Agric. Res. 1:215, 2012. (3) E. Punithalingam. Plant diseases attributed to Botryodiplodia theobromae Pat. J. Cramer, Vaduz, 1980.

No abstract

Samples of diseased plants were collected from 12 lettuce fields in Aydin province of the Aegean Region of Turkey. A total of 8 bacterial isolates were identified by morphological characterization, sequence analysis of 16S rDNA and gyrB genes, and pathogenicity. The survey included twelve lettuce fields of three different cultivars [Yedikule (romaine type), Robinson and Chianti (iceberg type)]. The incidence of the disease ranged from 48 to 95%. Plants of cv. Chianti were the most severely infected cultivars. To our knowledge, this is the first report of the presence of Xanthomonas hortorum pv. vitians in lettuce plants in Turkey.