The incidence of Alternaria spp. and Leptosphaeria maculans in commercial brassica seed in the United Kingdom

Tests on samples of oilseed rape seed ( Brassica napus ) sown in the UK between 1981 and 1984 indicated that on average 25% of samples were infected with Alternaria brassicae and 61% with Leptosphaeria maculans , with maximum incidences of infection of 19 and 4.2% respectively. Much infection by Alternaria spp. occurred on vegetable and forage brassica seed produced in the UK between 1979 and 1983. In B. oleracea types A. brassicicola occurred most frequently, affecting 88% of samples and up to 55% of seeds. A. brassicae was detected in 44% of B. oleracea samples and in up to 13% of seeds. Little Alternaria infection occurred in swede or forage rape samples (B. napus ), but A. brassicae affected up to 8–5% of seeds in turnip samples ( B. campestris ). L. maculans occurred in 44% of samples of vegetable and forage brassica seed produced in the UK, with a maximum of 4–6% infected seeds. A. brassicicola was present in 73% of samples of imported B. oleracea seed, affecting up to 25.5% of seeds. A. brassicae was absent from these samples and little L. maculans was detected. Pathogenicity tests on isolates of L. maculans from infected seeds indicated that virulent pathotypes were present in 16 rape seed samples but in only one sample (swede) of vegetable or forage brassica seed. The high incidence of seed infection by these pathogens emphasizes the importance of applying fungicide treatments to all types of brassica seed.     

Health of farmer-saved maize seed in north-east Nigeria

Many Nigerian farmers depend for their seed on seed-producing farmers, the so-called informal Seed System (SS), but seed quality of the SS is unknown. Farmers planting low quality seed risk poor field emergence and low plant vigour as a result of low physiological quality or infection with seed-borne pathogens. The objective of this research was to test seed quality of maize seed from the informal SS in north-east Nigeria. A total of 46,500 seeds (93 samples of 500 seeds each) were tested for germination, off-types and seed health. Seed pathology was quantified by plating disinfected seeds onto agar, and identifying the fungi present after 3 days incubation. Twelve seed-borne pathogens were identified including Bipolaris maydis (found in 45 % of the farmer-produced samples), Botryodiplodia theobromae (97 %) and Curvularia lunata (38 %). All samples were infected with Fusarium verticillioides, with a median infection incidence of 59 % (2009) and 51 % (2010). None of the 93 samples tested passed the demands for certified seed of the National Agricultural Seeds Council (NASC) in Nigeria, in particular the maximum limit of five off-types per kg seed sample. Based on these results, seed-producing farmers must improve the health of seed. The NASC should revise the standards for off-type seeds to minimize the time spent by farmers sorting planting material.     

Flower infection of Brassica oleracea with Xanthomonas campestris pv. campestris results in high levels of seed infection

During seed production, Brassica seed may become infected with Xanthomonas campestris pv. campestris after systemic colonization of plants upon leaf infection, or alternatively, after flower infection. Polytunnel experiments were conducted in 2007 and 2008 to study the relative importance of these colonization routes resulting in seed infection. Cauliflower plants (Brassica oleracea) were spray-inoculated at the 8-leaf stage, after formation of cauliflowers or during flowering, at which stage leaves or blossoms were inoculated. Inoculation at all stages resulted in a relatively high percentage of systemic infection; the average estimated infection incidences for stem base and peduncle infections were 16 % and 19 %, respectively. When seed samples were examined by dilution plating for deep-seated infection following hot water treatment, Xcc was detected in 61 % of the 23 seed samples harvested from plants with inoculated flowers. However, symptom development in seedlings raised from the seeds could not be confirmed in a grow-out test under favourable conditions for Xcc infection at a high RH (>95 %) and a relative high temperature (28 °C). Xcc was not detected in 59 seed samples harvested from leaf-inoculated plants with the exception of one sample from plants inoculated at peduncle formation. In a third polytunnel experiment carried out in 2009, the population dynamics of Xcc on inoculated flowers was investigated. Following spray-inoculation of flowers, 52 % of the flowers were infected with Xcc. During development of siliques, infection incidence decreased slowly and at 56 dpi, 20 % of the superficially disinfected siliques were infected with Xcc. It was estimated that 0.18 % of the seeds was infected and that 1–10 % of the infected siliques contained infected seeds. The implications of these results for control of Xcc in a seed production crop are discussed.     

Factors impacting the detection of weed seed contaminants in seed lots

BACKGROUND

The setting and following of phytosanitary standards for weed seeds can lessen the impacts of weeds on agriculture. Standards adopted by seed companies, laboratories and regulators ensure the contamination rates do not exceed some thresholds. Globally sample size standards are set based on the amount needed to obtain a contaminant in a random sample of the seed lot, not detectability. New Zealand requires a 95% confidence that the maximum pest limit of 0.01% of quarantine weed seed contamination is not exceeded in an imported seed lot. We examined 24 samples each containing approximately 150 000 seeds of either perennial ryegrass (12 samples) or white clover seeds (12 samples) that were then spiked with seeds (contaminants) from 12 non-crop species (3–8 seeds of each). We considered factors that may impact detection rates: shape, color, size, and texture relative to the crop, and technician (including a commercial seed laboratory).

RESULTS

A linear mixed model fitted to the data indicated significant observer, crop, and seed color, shape, and size effects on detection. Detectability increased by 20% ± 7.7 (± standard error) when seeds had a distinct shape or color (28% ± 8.1), or were larger (23% ± 8.7) rather than smaller, relative to the crop. Commercial laboratory identifications were usually correct at the level of genus, and species for common weeds, but some misidentifications occurred.

CONCLUSION

Sample sizes for border inspections should be based on detectability of regulated weed seeds in the crop in combination with weed risk for the crop and location. © 2022 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.     

Colonization of citrus seed coats by 'Candidatus Liberibacter asiaticus': implications for seed transmission of the bacterium

Huanglongbing is an economically damaging disease of citrus associated with infection by 'Candidatus Liberibacter asiaticus'. Transmission of the organism via infection of seeds has not been demonstrated but is a concern since some citrus varieties, particularly those used as rootstocks in commercial plantings are propagated from seed. We compared the incidence of detection of 'Ca. Liberibacter asiaticus' DNA in individual fruit peduncles, seed coats, seeds, and in germinated seedlings from 'Sanguenelli' sweet orange and 'Conners' grapefruit fruits sampled from infected trees. Using real-time quantitative PCR (qPCR) we detected pathogen DNA in nucleic acid extracts of 36 and 100% of peduncles from 'Sanguenelli' and from 'Conners' fruits, respectively. We also detected pathogen DNA in extracts of 37 and 98% of seed coats and in 1.6 and 4% of extracts from the corresponding seeds of 'Sanguenelli' and 'Conners', respectively. Small amounts of pathogen DNA were detected in 10% of 'Sanguenelli' seedlings grown in the greenhouse, but in none of 204 extracts from 'Conners' seedlings. Pathogen DNA was detected in 4.9% and in 89% of seed coats peeled from seeds of 'Sanguenelli' and 'Conners' which were germinated on agar, and in 5% of 'Sanguenelli' but in none of 164 'Conners' seedlings which grew from these seeds on agar. No pathogen DNA was detected in 'Ridge Pineapple' tissue at 3 months post-grafting onto 'Sanguenelli' seedlings, even when pathogen DNA had been detected initially in the 'Sanguenelli' seedling. Though the apparent colonization of 'Conners' seeds was more extensive and nearly uniform compared with 'Sanguenelli' seeds, no pathogen DNA was detected in 'Conners' seedlings grown from these seeds. For either variety, no association was established between the presence of pathogen DNA in fruit peduncles and seed coats and in seedlings.     

Comparison of visual head blight ratings, seed infection levels, and deoxynivalenol production for assessment of resistance in cereals inoculated with Fusarium culmorum

Seven spring wheat, 13 barley, 14 oats and 20 winter wheat genotypes were inoculated at flowering in 1993 and 1994 with mixed conidial suspensions of 8 isolates of Fusarium culmorum. Four weeks after inoculation, head blight was recorded in the field. After harvest, seed infection was assessed by a Freezing Blotter Test in the laboratory. Seed samples were also analyzed for deoxynivalenol (DON) content. Differences were found in head blight rating, the levels of infected seeds and the DON content between wheat, barley, and oats and between cultivars. Highly significant correlations were found between the percentage of heavily infected seed and the DON content. The weighted mean value of infected seeds and DON content were also significantly correlated. No significant correlation was found between head blight rating in the field and DON content. The level of infected seeds, as determined by the Freezing Blotter Test, was a better indication of the DON content in the seeds than the head blight rating. This visual assessment of levels of infected seeds gives a reliable estimate of resistance to Fusarium.     

A real-time PCR assay for detection and quantification of Verticillium dahliae in spinach seed

Verticillium dahliae is a soilborne fungus that causes Verticillium wilt on multiple crops in central coastal California. Although spinach crops grown in this region for fresh and processing commercial production do not display Verticillium wilt symptoms, spinach seeds produced in the United States or Europe are commonly infected with V. dahliae. Planting of the infected seed increases the soil inoculum density and may introduce exotic strains that contribute to Verticillium wilt epidemics on lettuce and other crops grown in rotation with spinach. A sensitive, rapid, and reliable method for quantification of V. dahliae in spinach seed may help identify highly infected lots, curtail their planting, and minimize the spread of exotic strains via spinach seed. In this study, a quantitative real-time polymerase chain reaction (qPCR) assay was optimized and employed for detection and quantification of V. dahliae in spinach germplasm and 15 commercial spinach seed lots. The assay used a previously reported V. dahliae-specific primer pair (VertBt-F and VertBt-R) and an analytical mill for grinding tough spinach seed for DNA extraction. The assay enabled reliable quantification of V. dahliae in spinach seed, with a sensitivity limit of ≈1 infected seed per 100 (1.3% infection in a seed lot). The quantification was highly reproducible between replicate samples of a seed lot and in different real-time PCR instruments. When tested on commercial seed lots, a pathogen DNA content corresponding to a quantification cycle value of ≥31 corresponded with a percent seed infection of ≤1.3%. The assay is useful in qualitatively assessing seed lots for V. dahliae infection levels, and the results of the assay can be helpful to guide decisions on whether to apply seed treatments.     

Comparison of extraction procedures and determination of the detection threshold for Clavibacter michiganensis ssp. michiganensis in tomato seeds

Several seed extraction procedures, used for detection of Clavibacter michiganensis ssp. michiganensis ( Cmm ) in naturally infected and artificially infested tomato seed lots were evaluated. Extraction methods that included grinding the seeds were significantly better at detecting the pathogen in three different seed lots than methods that used only soaking. The detection threshold of Cmm in relation to seed sample size was determined by adding naturally infected seeds into samples of three different sizes. Cmm was detected by agar plating assay, on three media (CNS, mSCM, D₂ANX), and by direct PCR from seeds and Bio-PCR (bacteria cultured on agar media prior to PCR). In samples of 10 000 seeds containing one infected seed, Cmm could be detected only by Bio-PCR and in only one replicate out of five. In samples containing five or 10 infected seeds per 10 000 seeds, three of five and five of five replicates, respectively, were detected by the three detection methods. In samples of 5000 seeds, one infected seed could be detected in all five replicates only after adding a concentration step. A high correlation ( R ² = 0·9448) between artificially infested seeds and the disease incidence was found. Seed lots infested with less than 58 colony-forming units (CFU) per g did not cause disease under glasshouse conditions, whereas lots with about 1000 CFU g⁻¹ caused disease in 78 plants out of 2000.     

<Emphasis Type="Italic">Indian citrus ringspot virus:</Emphasis> localization of virus in seed tissues and evidence for lack of seed transmission

Indian citrus ringspot disease is an important viral disease in kinnow mandarin orchards where disease incidence up to 100% has been recorded. The disease is caused by Indian citrus ringspot virus (ICRSV), a positive sense flexuous RNA virus. The transmission of ICRSV is generally through budwood. Association of ICRSV with pollens of naturally infected flowers from cv. ‘Kinnow’ mandarins has been shown previously and this study demonstrates the presence of ICRSV in seed tissues. DAC-ELISA revealed the presence of virus in seed coats but not in embryo and endosperm of seeds collected from the fruits of ICRSV-infected Kinnow plants. Of the infected seed coats, 18% were found to harbor the virus. The seedlings in the grow-out test did not show any symptom for 2 years and the virus could not be detected in seedlings by DAC-ELISA and RT-PCR. The present study indicated that ICRSV could be localized in the testa of seeds but its transmission to progeny was not observed.     

进境苇状羊茅和多年生黑麦草种子携带内生真菌带菌率的研究

苇状羊茅内生真菌和多年生黑麦草内生真菌曾给一些国家的畜牧业造成巨大损失.为防止内生真菌随进境草籽传入我国并在中国扩散危害,我们对该2种进境草籽内生真菌的带菌率进行了研究.首先通过分离培养,得到了苇状羊茅内生真菌和黑麦草内生真菌,然后采用染色法对1998年以来收集到的从天津口岸进境的部分苇状羊茅和黑麦草种子进行了初步检验,经检验,37份苇状羊茅样品中有18个品种带菌,34份多年生黑麦草样品中14个品种带菌,带菌率最高可达86.7%.早熟禾、剪股颖等其它禾本科草籽目前尚未发现带有内生真菌.     

Tracing seed to seedling transmission of the wheat blast pathogen Magnaporthe oryzae pathotype Triticum

Wheat blast caused by Magnaporthe oryzae pathotype Triticum (MoT), initially restricted to South America, is a global threat for wheat after spreading to Asia in 2016 by the introduction of contaminated seeds, raising the question about transmission of the pathogen from seeds to seedlings, a process so far not well understood. We therefore studied the relationship between seed infection and disease symptoms on seedlings and adult plants. To accomplish this objective, we inoculated spikes of wheat cv. Apogee with a transgenic isolate (MoT-DsRed, with the addition of being resistant to hygromycin). We identified MoT-DsRed in experiments using hygromycin resistance for selection or by observation of DsRed fluorescence. The seeds from infected plants looked either apparently healthy or shrivelled. To evaluate the transmission, two experimental designs were chosen (blotter test and greenhouse) and MoT-DsRed was recovered from both. This revealed that MoT is able to colonize wheat seedlings from infected seeds under the ground. The favourable conditions of temperature and humidity allowed a high recovery rate of MoT from wheat shoots when grown in artificial media. Around 42 days after germination of infected seeds, MoT-DsRed could not be reisolated, indicating that fungal progression, at this time point, did not proceed systemically/endophytically. We hypothesize that spike infection might occur via spore dispersal from infected leaves rather than within the plant. Because MoT-DsRed was not only successfully reisolated from seed coats and germinating seeds with symptoms, but also from apparently healthy seeds, urgent attention is needed to minimize the risks of inadvertent dispersal of inoculum.     

The question of seed transmissibility of Plum pox virus

For many years, Plum pox virus (PPV) was considered to be transmissible by seed, increasing the fear of long-distance spread of the disease. In the late 1970s, it was claimed on the basis of biological transmission of the virus to herbaceous indicator plants and the development of serological diagnosis based on polyclonal antibodies, that PPV was seed-transmitted, with a different infection rate according to the plant species and part of the seed which was tested. In the 1990s, PPV was characterized into four different types, and specific monoclonal antibodies were produced for them. These new and more sensitive diagnostic techniques, together with RT-PCR with different sets of specific primers, were used to approach once again the problem of PPV transmission through seeds. The virus was detected in seed coats and cotyledons, but embryonic tissue and seedlings obtained from germinated seeds never showed symptoms, and gave negative results for PPV with both ELISA and PCR assays. No PPV isolate is currently recognized to be seed transmitted, so vertical transmission of PPV from infected mother plants to their progeny does not occur. Hypothetically, the only possibility of seed transmission would arise from a mutation in the helper component of the virus, associated with high susceptibility of the infected Prunus cultivar.     

Effects of the seed weight and burial depth on the seed behavior of common ragweed (Ambrosia artemisiifolia)

Common ragweed (Ambrosia artemisiifolia L.) is one of the annual plants that were described recently as invasive weeds in Europe. This species is described as an invasive plant that produces seeds that are highly variable. Its production of variably sized seeds is regarded as promoting its spread in different environments. Experiments were carried out to determine the influence of the seed weight and temperature on germination and the influence of the seed weight and burial depth on seedling emergence. The seeds were divided into a number of classes of weight and the seed weight effect on germination was evaluated by Petri dish assays. In another experiment, the seeds were buried at different depths in a clay soil/sand mix to estimate the burial effect on germination and seedling emergence. The germination level of A. artemisiifolia was high overall, between 76.8% and 94.2%. The seed germination was modified by temperature but it was not influenced by the seed weight. The amounts of germination and seedling emergence were greater for the seeds on the soil surface and decreased with an increasing burial depth, from 2 to 8 cm. No germination or emergence was observed for the seeds that were buried at 10 and 12 cm. The lightest seeds were more sensitive to burial. A greater level of seedling emergence for those seeds that were placed near the soil surface could explain the success of this species in open habitats, where the probability of deeper burial is low. After high seed production, the management of A. artemisiifolia in fields could be partly achieved through soil tillage, burying seeds below 10 cm, and not carrying out deep soil tillage the following year.     

Infection of sesame seed by Alternaria sesami (Kawamura) Mohanty and Behera and severity of Alternaria leaf spot in Kenya

Infection levels of Alternaria sesami in sesame (Sesamum indicum L.) seeds collected from farmers in western districts of Kenya were detected using the oatmeal agar plate method. Infection levels varied from 9% in Kakamega to 24% in Siaya. Samples from Busia had a mean infection level of 11.69%. Alternaria leaf spot was monitored in plots planted with Alternaria sesami infected seed at six different infection levels at Kibwezi to determine the effect of transmission of the fungus by seed on disease severity. Increase in per cent leaf area blighted and per cent defoliation fit more closely the Gompertz model than the logistic model. Rates of disease increase in blighted leaf areas and defoliation, and areas under disease progress curves (AUDPC), varied among the six seed infection levels. Infection levels with larger AUDPC generally had faster rates of disease progress. Disease was most severe on plants established from seeds with 8% infection and least on plants established from seeds with 0% infection. Disease severity increased with increased seed infection level.     

Seed transmission of Melon necrotic spot virus and efficacy of seed-disinfection treatments

Rates of seed transmission of Melon necrotic spot virus (MNSV) were estimated in seedlings grown from commercial melon ( Cucumis melo ) cv. Galia F₁ seeds. Seedlings at the cotyledon stage and adult plants were assayed for MNSV by DAS-ELISA and RT-PCR. None of the seedling groups tested positive for MNSV by ELISA. The proportion of seedlings infected with MNSV was at least 7 and 8% in seed lots 05 and 06, respectively, as estimated from RT-PCR analysis of grouped seedlings. Fourteen and eight grouped samples (10 seedlings per group), of a total of 200 and 100 seedlings, respectively, grown from infected seeds were MNSV-positive in seed lots 05 and 06, respectively, corresponding to seed-to-seedling transmission rates of 11·3 and 14·8%, respectively. Several seed-disinfection treatments were evaluated for their ability to prevent seed transmission of MNSV. The results suggest that a treatment of 144 h at 70°C can be used to eradicate MNSV in melon seeds without hindering germination.     

The infestation of tomato seed by Fusarium oxysporum f.sp. radicis-lycopersici

The infestation of seed by Fusarium oxysporum f.sp. radicis-lycopersici occurred at rates of 0-1 to 0-01 % in fruit on stem-infected plants. Direct infection of fruit in the flower or young developing fruit stage resulted in a grayish-brown lesion on the stylar end of the fruit or mummification. F. oxysporum f.sp. radicis-lycopersici was isolated from all seeds in such fruit. Picked fruit inoculated on the stem scar also became infected but 96 h after inoculation of the fruit, the seed was not infested or infected. The contact of clean seed with hands that had previously handled F. oxysporum f.sp. radicis-lycoperisid-infesied sawdust resulted in a high level of seed infestation. The fungus survived on seed sent across Canada and stored for up to 12 weeks. Treatment with NaOCl or 0·1 N HCl did not completely disinfest infested seed.     

Summer-grown seed potatoes: an attempt to produce seed for the spring season in Israel

Seed potatoes were grown in Israel during summer (June-October) at Ramat haNegev (the Negev plateau). This is the hottest season in the semi-arid climate prevailing in the region. Because of the high temperature, no tuberization occurred in cv. ‘Up-to-Date; and ‘Draga’ and ‘Cara’ showed a marked yield reduction. Reasonable yields were, however, obtained at Ramat haNegev during summer growth with the cvs. ‘Désirée’, ‘Blanka’, ‘Spunta’ and ‘Alpha’. At Bet Dagan (coastal plain) Désirée grown during summer met with many problems and yields were negligible, probably because of the higher night temperature as compared with Ramat haNegev. Growth during summer in Ramat haNegev offers the advantages of relative isolation from other potato fields (potatoes are not grown in summer) and low aphid activity, in contrast to the common growing seasons — spring and autumn. Insecticide application and planting high quality seeds — imported elite or Class A — in summer, reduced potato leaf roll virus (PLRV) infection to an average of 4.5% in 1984 and 1.8% in 1985, in comparison with an average of 20.8% in 1979, when poor quality seeds were used and no insecticides were applied. Infection with potato virus Y (PVY) was 1.7% in 1984 and 0.1% in 1985. The yielding capacity in spring 1980 of seed potato produced at Ramat haNegev in the summer of 1979, was significantly lower than that of imported and Golan Heights seed. This is attributed mainly to the high level of virus infection of the former seeds. PLRV-free seed potatoes from the same batch yielded similarly to imported seed potatoes or seed potatoes from the Golan Heights. This was reconfirmed in the 1985 experiment in which Ramat haNegev seeds were much less infected with PLRV and produced yields similar to the imported and Golan ones. Seed potatoes from Ramat haNegev behave like young seeds when planted in the spring. Therefore, their yielding capacity probably increases the earlier the harvest and the longer the subsequent growing period.     

Passalora blight of anise (Pimpinella anisum) and its control in Turkey

Passalora blight of anise, caused byPassalora malkoffii (Bubák) U. Braun, is an important disease of anise in Turkey. The disease affects all the aboveground parts of plants including flower clusters. Infected seeds have dark, linear stromata. Detection of the pathogen on seeds was studied by the blotter method, agar method, washing test and sowing infected seeds in disease-free soils. The pathogen was recovered only by the washing test and to a limited extent by water agar + seed decoction agar. Sixteen of 24 seed samples from diseased regions were found to be infected. The pathogen was not detected by any other methods. However, several indigenous fungi,e.g. Alternaria alternata, were isolated, which may have prevented the growth of the pathogen. Seed washings of infected seed samples had typical spores of the pathogen up to 10⁶ conidia per gram of seed. Transmission of the pathogen was shown by sowing infected seeds in disease-free field soils in two locations where anise had not been grown previously. Azoxystrobin, chlorothalonil + carbendazim and flutriafol seed treatments at 0.04 g a.i. kg⁻¹ seed, 1.0 g + 4.5 g a.i. kg⁻¹ seed and 0.015 g a.i. kg⁻¹ seed reduced the disease by 92.5%, 89.6% and 36.2% in 2002 and by 78.9%, 75.8% and 41.2% in 2003, respectively. Three foliar applications of axosystrobin, chlorothalonil + carbendazim and flutriafol at the rates of 187.5 g a.i. ha⁻¹, 1500 g + 6750 g a.i. ha⁻¹ and 31.3 g a.i ha⁻¹ reduced disease incidence by 92.5%, 86.0% and 96.8% in 2002 and by 97.5%, 90.8% and 97.0% in 2003, respectively. http://www.phytoparasitica.org posting May 17, 2005.     

Relationships between seed germination, fumonisin content, and Fusarium verticillioides infection in selected maize samples from different regions of Costa Rica

Thirty-five maize seed samples from three geographic regions of Costa Rica were analysed for fumonisin content, germinability, and Fusarium verticillioides infection with and without surface disinfection. The concentration of fumonisins in the maize samples varied from 4 ng g⁻¹ to 16 000 ng g⁻¹ with an all over-all average of 2500 ng g⁻¹. There was a significant difference in fumonisin content between samples from Alajuela and Guanacaste. Germination of the seed samples ranged from 12% to 98% with significant differences between regions. F. verticillioides infection was 12–98% and 13–97% for surface-disinfected and nondisinfected seeds, respectively. There was a significant negative correlation ( r  = -0.52) between fumonisin content and seed germination, but no significant correlation was found between fumonisin content and F. verticillioides infection, or between F. verticillioides infection and seed germination. Most of the high fumonisin seed samples had some mechanical or insect damage. Whether or not the fumonisins had a direct effect on germination was not further established. It is concluded that the large differences in fumonisin content of maize seeds within and between regions are primarily caused by differences in seed quality, genetic diversity of F. verticillioides strains in natural populations, climatic differences between regions, and varietal differences. Some of the fumonisin levels found in this study coincide with levels associated with risks to humans and animals in other countries.     

Role of seed infection by the Ascochyta blight pathogen of dried pea (Mycosphaerella pinodes) in seedling emergence, early disease development and transmission of the disease to aerial plant parts

The role of infected seed in the epidemiology of Ascochyta blight of pea, caused by Mycosphaerella pinodes, was studied both under growth chamber and field conditions, using healthy seeds, naturally infected seeds and artificially infected seeds. Results suggest that infected seeds caused serious losses, as a result of poor germination and high transmission of the disease, to parts of the plants under soil level. Foot rot symptoms often caused the death of young seedlings. Losses were increased by low temperatures during the early stage of crop development. M. pinodes progressed from seeds to aerial parts of the plants, but no Ascochyta blight symptoms occurred, the disease remaining near to the basal parts of the plants as a foot rot symptom. This suggests that seeds cannot be regarded as a source of contamination in the epidemiology of the disease.