- 2021 - 2024 Can the identical gene allow adaptation to different environments? : Taking rheophytic and serpentine ecotypes as examples
- 2019 - 2022 Tolerance evaluation of broad-leaved teree species and possibility of establishing disaster resilient coastal forest
- 2018 - 2021 Comparative study of plant adaptation processes in riverside and serpentine areas
- 2017 - 2020 Analyses of effects of plant-microbe interactions in rhizosphere on evolution of plant-phytophagous insect interactions
- 2014 - 2017 Evolutionary processes of symbiotic interactions between parasitic plants and endophytic fungi.
- 2015 - 2017 ダムによる水量調節が河川沿いに生育が特化した植物の生育に与える影響の評価
- 2013 - 2016 Comparative morphology of leaves among ecotypes of rheophytic and serpentine environments
- 2012 - 2015 サゴヤシ野生林の実態解明と持続的利用に関する研究
- 2011 - 2014 Evolution of dynamics of plant-mycorrhizal fungi-endophyte triadic relationships in heterotrophic plants
- 2012 - 2013 河川沿いに特化した植物群の形態学的および遺伝学的比較による河川環境の多様性創出機構の解明
- 2010 - 2013 Accumulation of Curcumin and its genetic variation in medicinal plant Curcuma species
- 2010 - 2012 Evolutionary developmental background of morphological adaptation of Heteropappus species(Asteraceae)
- 2008 - 2011 菌根菌が超集積植物ヘビノネゴザの重金属、ヒ素集積に与える影響
- 2008 - 2011 Evolution of plant heterotrophy from autotrophy in plant-arbuscular mycorrhizal fungi mutualistic systems.
- 2008 - 2011 Host utilization by Nealsomyia rufella (Diptera ; Tachinidae)-Why does not the bagworm, Eumeta japonica (Lepidoptera ; Psychidae), become extinct in Kochi Prefecture?-
- 2008 - 2010 Evolutionary developmental study of Heteropappus species (Asteraceae)
- 2006 - 2010 土着天敵クロヒョウタンカスミカメの生物農薬として の利用
- 2006 - 2008 キク科ハマベノギク属の形態的適応に関する研究
- 2003 - 2006 花の相称性を支配する遺伝的メカニズムとその進化機構の解明
Show all