Currently the soybean crop is affected by the white mold (Sclerotinia sclerotiorum). The disease can reduce the crop yield and quality and decrease the prices of agricultural lands. The aim of the current research was...Currently the soybean crop is affected by the white mold (Sclerotinia sclerotiorum). The disease can reduce the crop yield and quality and decrease the prices of agricultural lands. The aim of the current research was to assess epidemiology of white mold on soybean crop grown at Arapoti, PR, Brazil, utilizing data related to agricultural practices and local meteorological factors. The experiment was conducted in a naturally infested area. The soybean crop was sown on October 18th, 2011. The experimental design adopted herein was a randomized block in a factorial combination with 4 row spacings (0.35, 0.45, 0.60, 0.75 m) and 4 plant populations (150, 200, 250, 300 thousand plants per hectare) and 4 replications. The temporal analysis of the epidemic was evaluated using mathematical models, such as Logistics, Monomolecular and Gompertz, in order to determine the best model that described the progress of the disease as a function of local meteorological elements. For the incidence data it has been shown that both logistic and monomolecular models were those that were best fitted to the experimental data. For severity, the best model related to the experimental data was the logistic one. Either for incidence or for severity, air temperature was considered to be the environmental factor most affecting the progress of the disease. The variability in the apparent infection rates of white mold on soybean was not affected by different row spacings and plant populations;therefore, suggesting that macroclimatic variations prevailed in such a fashion to mitigate the effect of cultural practices adopted in the field.展开更多
The genetic diversity and genetic structure of a population of isolates of Sclerotinia sclerotiorum (Lib.) de Bary from different regions and host plants were investigated using the random amplified polymorphic DNA (R...The genetic diversity and genetic structure of a population of isolates of Sclerotinia sclerotiorum (Lib.) de Bary from different regions and host plants were investigated using the random amplified polymorphic DNA (RAPD) method with 20 random decamer primer pairs in order to provide some information on the phylogenetic taxa and breeding for resistance to sclerotinia stem rot. A minimum of three and a maximum of 15 unambiguously amplified bands were generated, furnishing a total of 170 bands ranging in size from 100 to 3 200 bp, corresponding to an average of 8.5 bands per primer pair. One hundred and four of these 170 bands (61.2%) were polymorphic, the percentage of polymorphic bands for each primer pair ranging from 0.0% to 86.7%. The genetic relationships among the isolates, based on the results of RAPD analysis, were examined. The genetic similarity of all selected isolates was quite high. At the species level, the genetic diversity estimated by Nei's gene diversity (h) was 0.197 and Shannon's index of diversity (I) was 0.300. The unweighted pair-group mean analysis (UPGMA) cluster analysis showed that most isolates from the same regions were grouped in the same cluster or a close cluster. The population of isolates from Hefei (Anhui Province, China) was more uniform and relatively distant to other populations. The Canadian population collected from carrot (Daucus carota var. sativa DC.) was relatively close to the Polish population collected from oilseed rape (Brassica napus L.) plants. There was no relationship between isolates from the same host plants. An analysis of molecular variance (AMOVA) revealed that the percentage of variance attributable to variation among and within populations was 50.62% and 49.38%, respectively. When accessions from China, Europe, and Canada were treated as three separate groups, the variance components among groups, among populations within groups, and within populations were ?0.96%, 51.48%, and 49.47%, respectively. The genetic differentiations among and within populations were highly significant (P < 0.001). Similarly, the coefficient of gene differentiation (Gst) in total populations calculated by population genetic analysis was 0.229 4, which indicated that the genetic variation among populations was 22.94%. The gene flow (Nm) was 1.68, which indicated that the gene permutation and interaction among populations was relatively high.展开更多
文摘Currently the soybean crop is affected by the white mold (Sclerotinia sclerotiorum). The disease can reduce the crop yield and quality and decrease the prices of agricultural lands. The aim of the current research was to assess epidemiology of white mold on soybean crop grown at Arapoti, PR, Brazil, utilizing data related to agricultural practices and local meteorological factors. The experiment was conducted in a naturally infested area. The soybean crop was sown on October 18th, 2011. The experimental design adopted herein was a randomized block in a factorial combination with 4 row spacings (0.35, 0.45, 0.60, 0.75 m) and 4 plant populations (150, 200, 250, 300 thousand plants per hectare) and 4 replications. The temporal analysis of the epidemic was evaluated using mathematical models, such as Logistics, Monomolecular and Gompertz, in order to determine the best model that described the progress of the disease as a function of local meteorological elements. For the incidence data it has been shown that both logistic and monomolecular models were those that were best fitted to the experimental data. For severity, the best model related to the experimental data was the logistic one. Either for incidence or for severity, air temperature was considered to be the environmental factor most affecting the progress of the disease. The variability in the apparent infection rates of white mold on soybean was not affected by different row spacings and plant populations;therefore, suggesting that macroclimatic variations prevailed in such a fashion to mitigate the effect of cultural practices adopted in the field.
基金Basic Research and Development Plan of China，国家科技攻关项目，the Sino-Polish Scientific and Technological Cooperation Project for 2004-2006，中国科学院资助项目
文摘The genetic diversity and genetic structure of a population of isolates of Sclerotinia sclerotiorum (Lib.) de Bary from different regions and host plants were investigated using the random amplified polymorphic DNA (RAPD) method with 20 random decamer primer pairs in order to provide some information on the phylogenetic taxa and breeding for resistance to sclerotinia stem rot. A minimum of three and a maximum of 15 unambiguously amplified bands were generated, furnishing a total of 170 bands ranging in size from 100 to 3 200 bp, corresponding to an average of 8.5 bands per primer pair. One hundred and four of these 170 bands (61.2%) were polymorphic, the percentage of polymorphic bands for each primer pair ranging from 0.0% to 86.7%. The genetic relationships among the isolates, based on the results of RAPD analysis, were examined. The genetic similarity of all selected isolates was quite high. At the species level, the genetic diversity estimated by Nei's gene diversity (h) was 0.197 and Shannon's index of diversity (I) was 0.300. The unweighted pair-group mean analysis (UPGMA) cluster analysis showed that most isolates from the same regions were grouped in the same cluster or a close cluster. The population of isolates from Hefei (Anhui Province, China) was more uniform and relatively distant to other populations. The Canadian population collected from carrot (Daucus carota var. sativa DC.) was relatively close to the Polish population collected from oilseed rape (Brassica napus L.) plants. There was no relationship between isolates from the same host plants. An analysis of molecular variance (AMOVA) revealed that the percentage of variance attributable to variation among and within populations was 50.62% and 49.38%, respectively. When accessions from China, Europe, and Canada were treated as three separate groups, the variance components among groups, among populations within groups, and within populations were ?0.96%, 51.48%, and 49.47%, respectively. The genetic differentiations among and within populations were highly significant (P < 0.001). Similarly, the coefficient of gene differentiation (Gst) in total populations calculated by population genetic analysis was 0.229 4, which indicated that the genetic variation among populations was 22.94%. The gene flow (Nm) was 1.68, which indicated that the gene permutation and interaction among populations was relatively high.
