Hippeastrum, a highly diverse genus in the Amaryllidaceae family, is a valuable ornamental bulbous flowering plant. Somatic embryogenesis(SE) is an efficient method for mass production of Hippeastrum plantlets. Previo...Hippeastrum, a highly diverse genus in the Amaryllidaceae family, is a valuable ornamental bulbous flowering plant. Somatic embryogenesis(SE) is an efficient method for mass production of Hippeastrum plantlets. Previous studies have been devoted to the in vitro propagation of Hippeastrum, but the SE and its regulatory networks are rarely reported. In this study, we established a direct SE method of Hippeastrum Bangkok Rose' using leaf bases as explants. MS supplemented with 1.00 mg·L^(-1)NAA +1.00 mg·L^(-1)KT + 0.25 mg·L^(-1)TDZ was the optimal medium for SE. Histological observations showed that the bipolar somatic embryo originated from the epidermal cell layer and underwent initiation,globular, scutellar and coleoptile stages. During SE, endogenous hormones of IAA, CTK, ABA, and SA were highly accumulated. Transcriptomic analysis revealed the genes encoding auxin biosynthesis/metabolic enzymes and efflux carriers were induced, while the auxin receptor of TIR1 and ARF transcriptional repressor of Aux/IAA were down-regulated and up-regulated, respectively, leading to suppression of auxin signaling. In contrast, cytokine signaling was promoted at the early stage of SE, as biosynthesis, transport, and signaling components were up-regulated.Various stress-related genes were up-regulated at the early or late stages of SE. Chromatin remodeling could also be dynamically regulated via distinct expression enzymes that control histone methylation and acetylation during SE. Moreover, key SE regulators, including WOXs and SERKs were highly expressed along with SE. Overall, the present study provides insights into the SE regulatory mechanisms of the Hippeastrum.展开更多
Huanglongbing(HLB)is the most destructive bacterial disease of citrus worldwide.While most citrus varieties are susceptible to HLB,Poncirus trifoliata,a close relative of Citrus,and some of its hybrids with Citrus are...Huanglongbing(HLB)is the most destructive bacterial disease of citrus worldwide.While most citrus varieties are susceptible to HLB,Poncirus trifoliata,a close relative of Citrus,and some of its hybrids with Citrus are tolerant to HLB.No specific HLB tolerance genes have been identified in P.trifoliata but recent studies have shown that constitutive disease resistance(CDR)genes were expressed at much higher levels in HLB-tolerant Poncirus hybrids and the expression of CDR genes was modulated by Candidatus Liberibacter asiaticus(CLas),the pathogen of HLB.The current study was undertaken to mine and characterize the CDR gene family in Citrus and Poncirus and to understand its association with HLB tolerance in Poncirus.We identified 17 CDR genes in two citrus genomes,deduced their structures,and investigated their phylogenetic relationships.We revealed that the expansion of the CDR family in Citrus seems to be due to segmental and tandem duplication events.Through genome resequencing and transcriptome sequencing,we identified eight CDR genes in the Poncirus genome(PtCDR1-PtCDR8).The number of SNPs was the highest in PtCDR2 and the lowest in PtCDR7.Most of the deletion and insertion events were observed in the UTR regions of Citrus and Poncirus CDR genes.PtCDR2 and PtCDR8 were in abundance in the leaf transcriptomes of two HLB-tolerant Poncirus genotypes and were also upregulated in HLB-tolerant,Poncirus hybrids as revealed by real-time PCR analysis.These two CDR genes seem to be good candidate genes for future studies of their role in citrus-CLas interactions.展开更多
The cultivated strawberry(Fragaria×ananassa)is consumed worldwide for its flavor and nutritional benefits.Genetic analysis of commercially important traits in strawberry are important for the development of breed...The cultivated strawberry(Fragaria×ananassa)is consumed worldwide for its flavor and nutritional benefits.Genetic analysis of commercially important traits in strawberry are important for the development of breeding methods and tools for this species.Although several quantitative trait loci(QTL)have been previously detected for fruit quality and flowering traits using low-density genetic maps,clarity on the sub-genomic locations of these QTLs was missing.Recent discoveries in allo-octoploid strawberry genomics led to the development of the IStraw90 single-nucleotide polymorphism(SNP)array,enabling high-density genetic maps and finer resolution QTL analysis.In this study,breeder-specified traits were evaluated in the Eastern(Michigan)and Western(Oregon)United States for a common set of breeding populations during 2 years.Several QTLs were validated for soluble solids content(SSC),fruit weight(FWT),pH and titratable acidity(TA)using a pedigree-based QTL analysis approach.For fruit quality,a QTL for SSC on linkage group(LG)6A,a QTL for FWT on LG 2BII,a QTL for pH on LG 4CII and two QTLs for TA on LGs 2A and 5B were detected.In addition,a large-effect QTL for flowering was detected at the distal end of LG 4A,coinciding with the FaPFRU locus.Marker haplotype analysis in the FaPFRU region indicated that the homozygous recessive genotype was highly predictive of seasonal flowering.SNP probes in the FaPFRU region may help facilitate marker-assisted selection for this trait.展开更多
Downy mildew(DM),caused by obligate parasitic oomycetes,is a destructive disease for a wide range of crops worldwide.Recent outbreaks of impatiens downy mildew(IDM)in many countries have caused huge economic losses.A ...Downy mildew(DM),caused by obligate parasitic oomycetes,is a destructive disease for a wide range of crops worldwide.Recent outbreaks of impatiens downy mildew(IDM)in many countries have caused huge economic losses.A system to reveal plant–pathogen interactions in the early stage of infection and quickly assess resistance/susceptibility of plants to DM is desired.In this study,we established an early and rapid system to achieve these goals using impatiens as a model.Thirty-two cultivars of Impatiens walleriana and I.hawkeri were evaluated for their responses to IDM at cotyledon,first/second pair of true leaf,and mature plant stages.All I.walleriana cultivars were highly susceptible to IDM.While all I.hawkeri cultivars were resistant to IDM starting at the first true leaf stage,many(14/16)were susceptible to IDM at the cotyledon stage.Two cultivars showed resistance even at the cotyledon stage.Histological characterization showed that the resistance mechanism of the I.hawkeri cultivars resembles that in grapevine and type II resistance in sunflower.By integrating full-length transcriptome sequencing(Iso-Seq)and RNA-Seq,we constructed the first reference transcriptome for Impatiens comprised of 48,758 sequences with an N50 length of 2060 bp.Comparative transcriptome and qRT-PCR analyses revealed strong candidate genes for IDM resistance,including three resistance genes orthologous to the sunflower gene RGC203,a potential candidate associated with DM resistance.Our approach of integrating early disease-resistance phenotyping,histological characterization,and transcriptome analysis lay a solid foundation to improve DM resistance in impatiens and may provide a model for other crops.展开更多
Powdery mildew(PM)caused by Podosphaera aphanis is a major fungal disease of cultivated strawberry.Mildew Resistance Locus O(MLO)is a gene family described for having conserved seven-transmembrane domains.Induced loss...Powdery mildew(PM)caused by Podosphaera aphanis is a major fungal disease of cultivated strawberry.Mildew Resistance Locus O(MLO)is a gene family described for having conserved seven-transmembrane domains.Induced loss-of-function in specific MLO genes can confer durable and broad resistance against PM pathogens.However,the genomic structure and potential role of MLO genes for PM resistance have not been characterized yet in the octoploid cultivated strawberry.In the present study,MLO gene families were characterized in four diploid progenitor species(Fragaria vesca,F.iinumae,F.viridis,and F.nipponica)and octoploid cultivated(Fragaria×ananassa)strawberry,and potential sources of MLO-mediated susceptibility were identified.Twenty MLO sequences were identified in F.vesca and 68 identified in F.×ananassa.Phylogenetic analysis divided diploid and octoploid strawberry MLO genes into eight different clades,in which three FveMLO(MLO10,MLO17,and MLO20)and their twelve orthologs of FaMLO were grouped together with functionally characterized MLO genes conferring PM susceptibility.Copy number variations revealed differences in MLO composition among homoeologous chromosomes,supporting the distinct origin of each subgenome during the evolution of octoploid strawberry.Dissecting genomic sequence and structural variations in candidate FaMLO genes revealed their potential role associated with genetic controls and functionality in strawberry against PM pathogen.Furthermore,the gene expression profiling and RNAi silencing of putative FaMLO genes in response to the pathogen indicate the function in PM resistance.These results are a critical first step in understanding the function of strawberry MLO genes and will facilitate further genetic studies of PM resistance in cultivated strawberry.展开更多
Developing CRISPR/Cas9-mediated non-transgenic mutants in asexually propagated perennial crop plants is challenging but highly desirable.Here,we report a highly useful method using an Agrobacterium-mediated transient ...Developing CRISPR/Cas9-mediated non-transgenic mutants in asexually propagated perennial crop plants is challenging but highly desirable.Here,we report a highly useful method using an Agrobacterium-mediated transient CRISPR/Cas9 gene expression system to create non-transgenic mutant plants without the need for sexual segregation.We have also developed a rapid,cost-effective,and high-throughput mutant screening protocol based on Illumina sequencing followed by high-resolution melting(HRM)analysis.Using tetraploid tobacco as a model species and the phytoene desaturase(PDS)gene as a target,we successfully created and expediently identified mutant plants,which were verified as tetra-allelic mutants.We produced pds mutant shoots at a rate of 47.5%from tobacco leaf explants,without the use of antibiotic selection.Among these pds plants,17.2%were confirmed to be non-transgenic,for an overall non-transgenic mutation rate of 8.2%.Our method is reliable and effective in creating non-transgenic mutant plants without the need to segregate out transgenes through sexual reproduction.This method should be applicable to many economically important,heterozygous,perennial crop species that are more difficult to regenerate.展开更多
A laboratory study was conducted to evaluate the effect of compost amendment on mobility and leaching potential of heavy metals, nitrogen (N) and phosphorus (P) from a peat-based commercial container medium containing...A laboratory study was conducted to evaluate the effect of compost amendment on mobility and leaching potential of heavy metals, nitrogen (N) and phosphorus (P) from a peat-based commercial container medium containing 700 g kg-1 peat, 200 g kg-1 perlite and 100 g kg-1 vermiculite at varying amendment rates of compost (0, 0.25, 0.50, 0.75 and 1.00 L L-1). Increasing compost amendment significantly and linearly increased the pH (P < 0.01), the total concentrations of organic carbon (P < 0.05), copper (Cu) (P < 0.01), cadmium (Cd) (P < 0.01), and lead (Pb) (P < 0.01), and increased the bulk density (P < 0.01) of the medium. The electrical conductivity (EC), and total N and P of the medium increased significantly (P < 0.01) and quadratically with increasing compost amendment. The relationship of the C/N ratio of the medium with the compost amendment rate was decreasing, significant (P < 0.01) and cubic, while that of the total Zn was increasing, significant (P < 0.01) and cubic. Extractable P, NO3-N, and NH4-N increased initially with an increasing compost amendment of up to 0.50 L L-1 and then decreased with further increasing compost rate. Increasing compost rates resulted in a highly significant (P < 0.01) and linear increase in total Cd, Cu, and Pb, and a highly significant (P < 0.01) and cubic increase in total Zn in the medium. Increasing compost rates also significantly (P < 0.01) increased extractable Cu (linearly) and Zn (quadratically), but significantly (P < 0.01) decreased extractable Pb (linearly). There was no significant effect of compost amendment on the extractable Cd concentration in the medium. However, with increasing compost rates from 0.25 to 1.00 L L-1, extractability of P, Cd, Cu, Pb and Zn (extractable concentration as a percent of total) was decreased, indicating that compost amendment could lower the leachability of these elements from the medium.展开更多
FHB is one of the most destructive diseases of wheat. Resistance testing depends strongly on inoculation methods, and on measured traits. Therefore a four-year (2009-2012) study was performed using spray inoculation +...FHB is one of the most destructive diseases of wheat. Resistance testing depends strongly on inoculation methods, and on measured traits. Therefore a four-year (2009-2012) study was performed using spray inoculation + polyethylene (PE) bag cover, spray inoculation + mist irrigation, and spawn method supported by mist irrigation on 40 genotypes, 20 from Hungary and 20 from IFA Tulln, Austria. Each year four isolates were used in artificial inoculations except the spawn method where stalk debris served the inoculum. Visual Fusarium head blight (FHB) scores, Fusarium damaged kernels (FDK) and deoxynivalenol (DON) contamination were checked. 7680 FHB and FDK, as well as 3840 DON analyses served as the background for the statistical evaluation. The most reliable method used was the spray + polyethylene (PE) bag;the other two were significantly poorer being valid for all traits. The FHB scores were the least reliable, whereas the FDK was much more consequent and the DON gave the best results. The FDK gave much better predictions for DON contamination than FHB. The cultivars responses correlated well at different epidemic severities. The presence of the kernel resistance was confirmed and a new trait as extra kernel susceptibility was described. Presence of DON resistance was confirmed again, and extra DON susceptibility was described as a new trait. DON performance varied on the most sensitive cultivar between 0.32 and 143 mg/kg (mean 17.52 mg/kg) and on the most resistant genotype between 0.00 and 18.19 mg/kg (mean 1.87 mg/kg). Correlations between stability and resistance level are r = 0.85 for FHB, 0.78 for FDK, and 0.88 for DON, all at a significance level of p = 0.001. The very close correlation between FDK and DON contamination (r = 0.81, p = 0.001) proves that control of DON contamination needs appropriate resistance. In the breeding program evaluation of FDK is the most important, and then DON will be decided. Variety registration must be updated;otherwise no improvement on the field will occur.展开更多
基金funded by Guangdong Basic and Applied Basic Research Foundation (Grant No.2023A1515010237)the 2021 Dongguan Provincial Rural Revitalization Program (Grant No.20211800400022)+2 种基金the Guangdong Key Technology Research and Development Program (Grant Nos.2020B020220005,2022B1111040003)the Guangdong Modern Agricultural Industry Technology System Program (Grant No.2023KJ121)the South China Botanical Garden,the Chinese Academy of Sciences (Grant No.QNXM-02)。
文摘Hippeastrum, a highly diverse genus in the Amaryllidaceae family, is a valuable ornamental bulbous flowering plant. Somatic embryogenesis(SE) is an efficient method for mass production of Hippeastrum plantlets. Previous studies have been devoted to the in vitro propagation of Hippeastrum, but the SE and its regulatory networks are rarely reported. In this study, we established a direct SE method of Hippeastrum Bangkok Rose' using leaf bases as explants. MS supplemented with 1.00 mg·L^(-1)NAA +1.00 mg·L^(-1)KT + 0.25 mg·L^(-1)TDZ was the optimal medium for SE. Histological observations showed that the bipolar somatic embryo originated from the epidermal cell layer and underwent initiation,globular, scutellar and coleoptile stages. During SE, endogenous hormones of IAA, CTK, ABA, and SA were highly accumulated. Transcriptomic analysis revealed the genes encoding auxin biosynthesis/metabolic enzymes and efflux carriers were induced, while the auxin receptor of TIR1 and ARF transcriptional repressor of Aux/IAA were down-regulated and up-regulated, respectively, leading to suppression of auxin signaling. In contrast, cytokine signaling was promoted at the early stage of SE, as biosynthesis, transport, and signaling components were up-regulated.Various stress-related genes were up-regulated at the early or late stages of SE. Chromatin remodeling could also be dynamically regulated via distinct expression enzymes that control histone methylation and acetylation during SE. Moreover, key SE regulators, including WOXs and SERKs were highly expressed along with SE. Overall, the present study provides insights into the SE regulatory mechanisms of the Hippeastrum.
基金ZD acknowledges financial support of this study from the Citrus Research and Development Foundation,Inc.(CDRF)(Project#108766 and#105077)from the USDA-NIFA Citrus Disease Research and Extension(CDRE)Program(Grant No.2015-70016-23027).
文摘Huanglongbing(HLB)is the most destructive bacterial disease of citrus worldwide.While most citrus varieties are susceptible to HLB,Poncirus trifoliata,a close relative of Citrus,and some of its hybrids with Citrus are tolerant to HLB.No specific HLB tolerance genes have been identified in P.trifoliata but recent studies have shown that constitutive disease resistance(CDR)genes were expressed at much higher levels in HLB-tolerant Poncirus hybrids and the expression of CDR genes was modulated by Candidatus Liberibacter asiaticus(CLas),the pathogen of HLB.The current study was undertaken to mine and characterize the CDR gene family in Citrus and Poncirus and to understand its association with HLB tolerance in Poncirus.We identified 17 CDR genes in two citrus genomes,deduced their structures,and investigated their phylogenetic relationships.We revealed that the expansion of the CDR family in Citrus seems to be due to segmental and tandem duplication events.Through genome resequencing and transcriptome sequencing,we identified eight CDR genes in the Poncirus genome(PtCDR1-PtCDR8).The number of SNPs was the highest in PtCDR2 and the lowest in PtCDR7.Most of the deletion and insertion events were observed in the UTR regions of Citrus and Poncirus CDR genes.PtCDR2 and PtCDR8 were in abundance in the leaf transcriptomes of two HLB-tolerant Poncirus genotypes and were also upregulated in HLB-tolerant,Poncirus hybrids as revealed by real-time PCR analysis.These two CDR genes seem to be good candidate genes for future studies of their role in citrus-CLas interactions.
基金This research was funded through the USDA’s National Institute of Food and Agriculture—Specialty Crop Research Initiative project,‘RosBREED:Enabling Marker-Assisted Breeding in Rosaceae’(2009-51181-05808)‘RosBREED:Combining Disease Resistance and Horticultural Quality in New Rosaceous Cultivars’(2014-51181-22378).
文摘The cultivated strawberry(Fragaria×ananassa)is consumed worldwide for its flavor and nutritional benefits.Genetic analysis of commercially important traits in strawberry are important for the development of breeding methods and tools for this species.Although several quantitative trait loci(QTL)have been previously detected for fruit quality and flowering traits using low-density genetic maps,clarity on the sub-genomic locations of these QTLs was missing.Recent discoveries in allo-octoploid strawberry genomics led to the development of the IStraw90 single-nucleotide polymorphism(SNP)array,enabling high-density genetic maps and finer resolution QTL analysis.In this study,breeder-specified traits were evaluated in the Eastern(Michigan)and Western(Oregon)United States for a common set of breeding populations during 2 years.Several QTLs were validated for soluble solids content(SSC),fruit weight(FWT),pH and titratable acidity(TA)using a pedigree-based QTL analysis approach.For fruit quality,a QTL for SSC on linkage group(LG)6A,a QTL for FWT on LG 2BII,a QTL for pH on LG 4CII and two QTLs for TA on LGs 2A and 5B were detected.In addition,a large-effect QTL for flowering was detected at the distal end of LG 4A,coinciding with the FaPFRU locus.Marker haplotype analysis in the FaPFRU region indicated that the homozygous recessive genotype was highly predictive of seasonal flowering.SNP probes in the FaPFRU region may help facilitate marker-assisted selection for this trait.
基金supported by grants from the Florida Department of Agriculture and Consumer Service(FDACS)Florida Specialty Crop Block Grant Program(FDACS contract#020705 to A.P.and Z.D.)the Fred C.Gloeckner Foundation,Inc.(Z.D.),and the USDA/NIFA hatch projects(Project#FLA-GCR-005065 and FLA-GCC-005507)(Z.D.)。
文摘Downy mildew(DM),caused by obligate parasitic oomycetes,is a destructive disease for a wide range of crops worldwide.Recent outbreaks of impatiens downy mildew(IDM)in many countries have caused huge economic losses.A system to reveal plant–pathogen interactions in the early stage of infection and quickly assess resistance/susceptibility of plants to DM is desired.In this study,we established an early and rapid system to achieve these goals using impatiens as a model.Thirty-two cultivars of Impatiens walleriana and I.hawkeri were evaluated for their responses to IDM at cotyledon,first/second pair of true leaf,and mature plant stages.All I.walleriana cultivars were highly susceptible to IDM.While all I.hawkeri cultivars were resistant to IDM starting at the first true leaf stage,many(14/16)were susceptible to IDM at the cotyledon stage.Two cultivars showed resistance even at the cotyledon stage.Histological characterization showed that the resistance mechanism of the I.hawkeri cultivars resembles that in grapevine and type II resistance in sunflower.By integrating full-length transcriptome sequencing(Iso-Seq)and RNA-Seq,we constructed the first reference transcriptome for Impatiens comprised of 48,758 sequences with an N50 length of 2060 bp.Comparative transcriptome and qRT-PCR analyses revealed strong candidate genes for IDM resistance,including three resistance genes orthologous to the sunflower gene RGC203,a potential candidate associated with DM resistance.Our approach of integrating early disease-resistance phenotyping,histological characterization,and transcriptome analysis lay a solid foundation to improve DM resistance in impatiens and may provide a model for other crops.
基金This work was supported by the Florida Strawberry Research and Education Foundation(FSREF)the“Next-generation Disease Resistance Breeding and Management Solutions for Strawberry”under award no.2017-51181-26833.
文摘Powdery mildew(PM)caused by Podosphaera aphanis is a major fungal disease of cultivated strawberry.Mildew Resistance Locus O(MLO)is a gene family described for having conserved seven-transmembrane domains.Induced loss-of-function in specific MLO genes can confer durable and broad resistance against PM pathogens.However,the genomic structure and potential role of MLO genes for PM resistance have not been characterized yet in the octoploid cultivated strawberry.In the present study,MLO gene families were characterized in four diploid progenitor species(Fragaria vesca,F.iinumae,F.viridis,and F.nipponica)and octoploid cultivated(Fragaria×ananassa)strawberry,and potential sources of MLO-mediated susceptibility were identified.Twenty MLO sequences were identified in F.vesca and 68 identified in F.×ananassa.Phylogenetic analysis divided diploid and octoploid strawberry MLO genes into eight different clades,in which three FveMLO(MLO10,MLO17,and MLO20)and their twelve orthologs of FaMLO were grouped together with functionally characterized MLO genes conferring PM susceptibility.Copy number variations revealed differences in MLO composition among homoeologous chromosomes,supporting the distinct origin of each subgenome during the evolution of octoploid strawberry.Dissecting genomic sequence and structural variations in candidate FaMLO genes revealed their potential role associated with genetic controls and functionality in strawberry against PM pathogen.Furthermore,the gene expression profiling and RNAi silencing of putative FaMLO genes in response to the pathogen indicate the function in PM resistance.These results are a critical first step in understanding the function of strawberry MLO genes and will facilitate further genetic studies of PM resistance in cultivated strawberry.
基金We thank the financial support from the USDA National Institute of Food and Agriculture SCRI(grant no.2015-70016-23027)the Florida Citrus Development Foundation(2016-001)+1 种基金the Genetically Modified Organisms Breeding Major Projects of China(2014ZX0801008B-001)The Connecticut-Storrs Agriculture Experimental Station,the Priority Academic Program Development of Jiangsu Higher Education Institutions and the Innovative Research Project of JAAS(ZX-17-2006)also contributed financially to some experiments presented in this manuscript.
文摘Developing CRISPR/Cas9-mediated non-transgenic mutants in asexually propagated perennial crop plants is challenging but highly desirable.Here,we report a highly useful method using an Agrobacterium-mediated transient CRISPR/Cas9 gene expression system to create non-transgenic mutant plants without the need for sexual segregation.We have also developed a rapid,cost-effective,and high-throughput mutant screening protocol based on Illumina sequencing followed by high-resolution melting(HRM)analysis.Using tetraploid tobacco as a model species and the phytoene desaturase(PDS)gene as a target,we successfully created and expediently identified mutant plants,which were verified as tetra-allelic mutants.We produced pds mutant shoots at a rate of 47.5%from tobacco leaf explants,without the use of antibiotic selection.Among these pds plants,17.2%were confirmed to be non-transgenic,for an overall non-transgenic mutation rate of 8.2%.Our method is reliable and effective in creating non-transgenic mutant plants without the need to segregate out transgenes through sexual reproduction.This method should be applicable to many economically important,heterozygous,perennial crop species that are more difficult to regenerate.
文摘A laboratory study was conducted to evaluate the effect of compost amendment on mobility and leaching potential of heavy metals, nitrogen (N) and phosphorus (P) from a peat-based commercial container medium containing 700 g kg-1 peat, 200 g kg-1 perlite and 100 g kg-1 vermiculite at varying amendment rates of compost (0, 0.25, 0.50, 0.75 and 1.00 L L-1). Increasing compost amendment significantly and linearly increased the pH (P < 0.01), the total concentrations of organic carbon (P < 0.05), copper (Cu) (P < 0.01), cadmium (Cd) (P < 0.01), and lead (Pb) (P < 0.01), and increased the bulk density (P < 0.01) of the medium. The electrical conductivity (EC), and total N and P of the medium increased significantly (P < 0.01) and quadratically with increasing compost amendment. The relationship of the C/N ratio of the medium with the compost amendment rate was decreasing, significant (P < 0.01) and cubic, while that of the total Zn was increasing, significant (P < 0.01) and cubic. Extractable P, NO3-N, and NH4-N increased initially with an increasing compost amendment of up to 0.50 L L-1 and then decreased with further increasing compost rate. Increasing compost rates resulted in a highly significant (P < 0.01) and linear increase in total Cd, Cu, and Pb, and a highly significant (P < 0.01) and cubic increase in total Zn in the medium. Increasing compost rates also significantly (P < 0.01) increased extractable Cu (linearly) and Zn (quadratically), but significantly (P < 0.01) decreased extractable Pb (linearly). There was no significant effect of compost amendment on the extractable Cd concentration in the medium. However, with increasing compost rates from 0.25 to 1.00 L L-1, extractability of P, Cd, Cu, Pb and Zn (extractable concentration as a percent of total) was decreased, indicating that compost amendment could lower the leachability of these elements from the medium.
文摘FHB is one of the most destructive diseases of wheat. Resistance testing depends strongly on inoculation methods, and on measured traits. Therefore a four-year (2009-2012) study was performed using spray inoculation + polyethylene (PE) bag cover, spray inoculation + mist irrigation, and spawn method supported by mist irrigation on 40 genotypes, 20 from Hungary and 20 from IFA Tulln, Austria. Each year four isolates were used in artificial inoculations except the spawn method where stalk debris served the inoculum. Visual Fusarium head blight (FHB) scores, Fusarium damaged kernels (FDK) and deoxynivalenol (DON) contamination were checked. 7680 FHB and FDK, as well as 3840 DON analyses served as the background for the statistical evaluation. The most reliable method used was the spray + polyethylene (PE) bag;the other two were significantly poorer being valid for all traits. The FHB scores were the least reliable, whereas the FDK was much more consequent and the DON gave the best results. The FDK gave much better predictions for DON contamination than FHB. The cultivars responses correlated well at different epidemic severities. The presence of the kernel resistance was confirmed and a new trait as extra kernel susceptibility was described. Presence of DON resistance was confirmed again, and extra DON susceptibility was described as a new trait. DON performance varied on the most sensitive cultivar between 0.32 and 143 mg/kg (mean 17.52 mg/kg) and on the most resistant genotype between 0.00 and 18.19 mg/kg (mean 1.87 mg/kg). Correlations between stability and resistance level are r = 0.85 for FHB, 0.78 for FDK, and 0.88 for DON, all at a significance level of p = 0.001. The very close correlation between FDK and DON contamination (r = 0.81, p = 0.001) proves that control of DON contamination needs appropriate resistance. In the breeding program evaluation of FDK is the most important, and then DON will be decided. Variety registration must be updated;otherwise no improvement on the field will occur.