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The New Phytologist|October 5, 2021
A dated phylogeny shows Plio-Pleistocene climates spurred evolution of antibrowsing defences in the New Zealand floraKévin J L Maurin, Rob D Smissen, Christopher H LuskThe New Phytologist|October 5, 2021
Pathogen-driven coevolution across the CBP60 plant immune regulator subfamilies confers resilience on the regulator moduleQi Zheng, Kristina Majsec, Fumiaki KatagiriThe New Phytologist|October 5, 2021
Correlations between allocation to foliar phosphorus fractions and maintenance of photosynthetic integrity in six mangrove populations as affected by chillingLi Yan, V S John Sunoj, Aidan W Short, et al.The New Phytologist|October 7, 2021
Physiological roles of Casparian strips and suberin in the transport of water and solutesMonica Calvo-Polanco, Zoe Ribeyre, Myriam Dauzat, et al.The New Phytologist|October 7, 2021
Methane emissions may be driven by hydrogenotrophic methanogens inhabiting the stem tissues of poplarHuili Feng, Jiahuan Guo, Xuehong Ma, et al.The New Phytologist|February 8, 2022
A cost-benefit analysis of leaf carbon economy with consideration of seasonal changes in leaf traits for sympatric deciduous and evergreen congeners: implications for their coexistenceYunhan Ye, Kanehiro Kitayama, Yusuke OnodaThe New Phytologist|February 4, 2022
Multivariate selection mediated by aridity predicts divergence of drought-resistant traits along natural aridity gradients of an invasive weedCarter Carvalho, Rochelle Davis, Tim Connallon, et al.The New Phytologist|June 21, 2019
Iron acquisition strategies in land plants: not so different after allLouis Grillet, Wolfgang SchmidtThe New Phytologist|June 22, 2019
Expecting the unexpected: factors influencing the emergence of fungal and oomycete plant pathogensPilar Corredor-Moreno, Diane G O SaundersPageof 1,257