LXV SIGA Annual Congress
“From genes to fork: On Mendel’s footsteps”
06-09 September 2022
SESSION 5 - New routes to plant adaptation and sustainable agriculture
ORAL COMMUNICATIONS5.01 | Reverse genetic tools and their utilization to dissect grain yield components in wheat |
5.02 | Exploring the molecular bases of Root Growth Angle and its regulation in barley and wheat |
5.03 | Barley germination after flooding events depends on hypoxia-induced secondary dormancy |
5.04 | Functional study of lipoxygenase-mediated resistance against Aspergillus flavus and Fusarium verticillioides infection in Maize |
5.05 | CRISPR/Cas9-mediated mutagenesis of a polyamine oxidase gene increases tomato plant tolerance to drought stress |
5.06 | Eremocitrus glauca, a genetic source to fight against Huanglongbing, a highly destructive citrus disease |
5.07 | Triticum aestivum subspecies: exploring ancient diversity |
5.08 | Transcriptomic analysis in response to long period of cadmium exposure reveals tolerance mechanisms involving the root cell wall lignification in Arundo donax L. |
5.09 | Screening of Solanum lycopersicum x Solanum pennellii introgression lines for the resistance versus the parasitic weed Phelipanche ramosa: a step towards dual RNA-sequencing aimed at studying host/parasite crosstalk |
5.10 | Novel protein fragments for tomato resilience to salt stress |
5.11 | Constitution of new genetic variability of wheat and legumes and selection of best performing genotypes for conventional agriculture |
5.12 | Chloroplast omics of endive ("Cichorium endivia" L.): characterising genome structural variants and transcriptome response to rainfall-induced waterlog stress. |
5.13 | Arabidopsis thaliana growth promotion and salt stress tolerance by the PGPR Beijerinckia fluminensis |
5.14 | New strategies for Botrytis Bunch Rot control for a sustainable viticulture |
5.15 | Transcriptional analysis of eight magic maize parental lines infected with Fusarium verticillioides |
5.16 | A pale green barley mutant to increase the albedo of cultivated areas and agriculture sustainability |
5.17 | Matching maize and soil microbiome to boost seed yield and quality |
5.18 | Marker-trait associations of agronomic traits from the Cerealmed durum wheat panel as assessed in multi-environment trials under conservative agriculture |
5.19 | Accelerate the identification and selection of drought resilience tomato genotypes through in vivo phenotyping |
5.20 | Water stress response evaluation in Olea europaea L . cultivars: a multidisciplinary approach |
5.21 | Evolutionary populations as a model for studying adaptation strategies towards drought-stress |
5.22 | Phenological and bioclimatic diversity reveal challenges and opportunities to adapt Ethiopian barley (Hordeum vulgare L.) to a changing climate |
5.23 | Italian maize germplasm enrichment and innovation through Italy – Bolivia cooperation project and EVA European maize network |
5.24 | Apulian olive germplasm as potential sources of resistance to Xylella fastidiosa |
5.25 | Simultaneous application of heat and drought stress on durum wheat-Thinopyrum ponticum recombinant lines revealed tolerance traits associated with presence of the wild 7el1 chromosome introgressions |
5.26 | Analysis of VvEPFL9-1 and VvEPFL9-2 expression in grapevine leaves and correlation with stomatal density |
5.27 | Genome editing protocols and genetic diversity tools for flowering time adaptation in Asteraceae |
5.28 | Metabolic GWAS of eggplant peel composition in a worldwide collection |
5.29 | Genome Wide Association analysis of agronomically relevant traits in an eggplant core collection representative of the worldwide genetic variation |
5.30 | Effects of nitrogen form supply on the response to Fusarium oxysporum f. sp. melongenae in eggplant lines carrying partial resistance |
5.31 | The miRNA397a/laccase regulatory module control kernel size and shape in barley |
5.32 | Water use efficiency of a spring 2-row barley population assessed in the PlantArray physiological phenotyping platform |
5.33 | Characterizing heterosis in a set of recombinant intercrosses (RIXs) developed from a multiparental maize population |
5.34 | Exploitation of genetic diversity of a tomato MAGIC Population through Genome wide association analysis |
5.35 | First overview of Chloride Channel (CLC) family members for their transcriptional differential responses to nitrate in NUE-contrasting eggplant genotypes |
5.36 | Development of a non-chemical RNAi-based strategy for Amaranthus hybridus L. weed management |
5.37 | Identification of a set of wide untapped diversity for reaction to tan spot in durum wheat |
5.38 | Analysis of salinity tolerance in tomato Introgression Lines (ILs) based on morpho-biometric parameters and differential gene expression |
5.39 | Unlocking the hidden potential of genetic diversity to improve durum wheat resistance to heat stress |
5.40 | MIRALO* - Analysis of maize inbred lines for the development of hybrids with efficient radical apparatus |
5.41 | Pulse thermography as a new tool for early detection of necrotrophic fungal infections in plants |
5.42 | Evaluation of ear rot resistance in Italian maize inbred lines and molecular characterization of Fusarium isolates* |
5.43 | Engineering water use in tomato by generating novel allelic variation of ABA signaling genes via Crispr-Cas9 |
5.44 | Key genes involved in cuticle deposition as target to manipulate leaf permeability and increase plant adaptation to environmental cues |
5.45 | Study of the ability in exploiting organic P sources by the fodder crops alfalfa and maize |
5.46 | The Smart-Breed Project: innovative molecular technologies for the adaptation of horticultural species to climate change through precision breeding |
5.47 | CRF (CYTOKININ RESPONSE FACTOR) transcription factors in abiotic-stress and flowering time: from Arabidopsis thaliana to Lactuca sativa and Solanum lycopersicum |
5.48 | Heterologous production of irregular monoterpenes in tobacco and benthamiana as precursors for the synthesis of mealybug pheromones. |
5.49 | Editing of the durum wheat PDIL5-1 gene to increase resistance to soil-borne bymoviruses |
5.50 | Investigating the role of GRF4 in Barley seed size determination |
5.51 | Browsing in the Global Durum Panel for resistance to soil-borne viruses |
5.52 | Genome wide association mapping of flowering-veraison interval in Vitis vinifera L |
5.53 | Application of Microbial Consortia and biochar for sustainable Lettuce and Rocket cultivation |
5.54 | Translating genomic information to Prunus breeding programs |
5.55 | Citizen science and participatory breeding activities within the HARNESSTOM project |
5.56 | Exploring the biodiversity of plant traits and microbiome in maize local varieties as novel tools to face environmental challenges |
5.57 | Genome-wide association mapping of root traits in durum wheat (Triticum durum) |
5.58 | Genome Wide Association study uncovers the QTLome for osmotic adjustment and related drought adaptive traits in durum wheat |
5.59 | Functional characterization of a tomato gluthathione S-transferase gene and its implication in the plant response to environmental stresses |
5.60 | Screening tomato glutathione S-transferase diversity for association to drought stress |
5.61 | Analysis of the reserve proteome of wheat flours (T. durum and T. aestivum) grown in the presence of biostimulants and amendments |
5.62 | Digital phenotypes during recurrent drought stress: screening of a tomato collection |
5.63 | Grape volatile metabolism: a comparative analysis of transcripts and metabolites’ profiles in Aglianico and Falanghina ripening berries |
5.64 | Forward and reverse genetics approaches for the characterization of barley plant architecture genes |
5.65 | CRISPR/Cas9 mediated generation of tomato elite-edited lines tolerant to multistresses |