about
Understanding the low photosynthetic rates of sun and shade coffee leaves: bridging the gap on the relative roles of hydraulic, diffusive and biochemical constraints to photosynthesisProtective Response Mechanisms to Heat Stress in Interaction with High [CO2] Conditions in Coffea sppSustained photosynthetic performance of Coffea spp. under long-term enhanced [CO2]Long-term elevated air [CO2 ] strengthens photosynthetic functioning and mitigates the impact of supra-optimal temperatures in tropical Coffea arabica and C. canephora species.Differentially expressed genes and proteins upon drought acclimation in tolerant and sensitive genotypes of Coffea canephoraSustained enhancement of photosynthesis in coffee trees grown under free-air CO2 enrichment conditions: disentangling the contributions of stomatal, mesophyll, and biochemical limitations.Improving the estimation of mesophyll conductance to CO₂: on the role of electron transport rate correction and respirationLimitations to photosynthesis in coffee leaves from different canopy positions.Could shading reduce the negative impacts of drought on coffee? A morphophysiological analysis.Enhanced Photosynthesis and Growth in atquac1 Knockout Mutants Are Due to Altered Organic Acid Accumulation and an Increase in Both Stomatal and Mesophyll Conductance.Drought tolerance is associated with rooting depth and stomatal control of water use in clones of Coffea canephora.Arabidopsis and tobacco plants ectopically expressing the soybean antiquitin-like ALDH7 gene display enhanced tolerance to drought, salinity, and oxidative stress.Magnesium decreases leaf scald symptoms on rice leaves and preserves their photosynthetic performance.Alterations in Gas Exchange and Oxidative Metabolism in Rice Leaves Infected by Pyricularia oryzae are Attenuated by Silicon.Photosynthesis and photoprotection in coffee leaves is affected by nitrogen and light availabilities in winter conditions.Soybean Resistance to Cercospora sojina Infection Is Reduced by Silicon.Asymmetrical effects of mesophyll conductance on fundamental photosynthetic parameters and their relationships estimated from leaf gas exchange measurements.Leaf gas exchange and oxidative stress in sorghum plants supplied with silicon and infected by Colletotrichum sublineolum.Limitations to photosynthesis in leaves of wheat plants infected by Pyricularia oryzae.Stomatal dynamics are limited by leaf hydraulics in ferns and conifers: results from simultaneous measurements of liquid and vapour fluxes in leaves.In field-grown coffee trees source-sink manipulation alters photosynthetic rates, independently of carbon metabolism, via alterations in stomatal functionSilicon nutrition increases grain yield, which, in turn, exerts a feed-forward stimulation of photosynthetic rates via enhanced mesophyll conductance and alters primary metabolism in riceDeficiency in silicon uptake affects cytological, physiological, and biochemical events in the rice--Bipolaris oryzae interactionLeaf gas exchange and chlorophyll a fluorescence in wheat plants supplied with silicon and infected with Pyricularia oryzaeSilicon nutrition alleviates the negative impacts of arsenic on the photosynthetic apparatus of rice leaves: an analysis of the key limitations of photosynthesisLeaf Gas Exchange and Chlorophyll a Fluorescence Imaging of Rice Leaves Infected with Monographella albescens
P50
Q28538019-A326C147-1F55-4409-ADAD-44016AC25862Q28597148-7E634080-C747-413B-A7A2-E43BDA5A87EFQ30712374-828E06EE-F9C3-429E-B95C-3F4212688C3BQ30993189-BDB709A4-85E6-4655-8C7E-9F127A123D6FQ34236525-0882AEEF-EEE4-4903-AF36-5FAA40CC6E75Q36380119-5DD96ECF-33AF-48AC-A819-20CE90969F15Q37069220-55C8C346-3969-4D51-9846-B4A56FDE1F25Q38878466-F5C7FEB8-40FC-4BF6-A4BB-E181C4C8F33DQ38935179-277F4885-858E-4062-8C3C-4A8462DE8159Q39239330-6F1A1E14-4401-4AD3-951C-974731230C11Q39356998-BDF6535B-00C2-4E76-BE99-33DB7BC22973Q39404225-8A7DB137-EA1D-4F44-9985-C54D4F9C0CBEQ40500637-283BEC07-7E61-49B2-A5C1-D4FFC43FD777Q41530497-FB5D612E-14DE-4B18-85E9-2A4451AE5FEAQ43104426-F1978015-A540-42AC-8018-CF0E4900DCF9Q46896880-9E473643-9740-4F3E-9D44-A9D34A2C1725Q46984048-46813DC4-AA0B-4C25-B26D-D77B575535F4Q47659680-D1FD2261-D1DE-4BBC-82F1-624EFFE36B7BQ47893318-7C0265E2-C89C-463E-8657-C173FA04F2B6Q53297220-34337553-DD34-4DC9-B691-EA0F050B9D45Q80677672-8CE07935-8C25-4637-95DA-04D1FD1BF73EQ85003951-CD910EE3-9FBE-43B4-971D-2FA47701DA19Q85109441-854F29B3-0933-496A-B993-7ADD9518BDAEQ85946097-8EF79EEE-D975-467A-9CFE-3B151C805457Q87396645-C8F421C1-1F10-49A6-AEF9-7599E0952184Q87672397-AB7648E6-9B87-41CB-9376-4A677B92C565
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Fábio M DaMatta
@en
Fábio M DaMatta
@nl
type
label
Fábio M DaMatta
@en
Fábio M DaMatta
@nl
prefLabel
Fábio M DaMatta
@en
Fábio M DaMatta
@nl
P31
P496
0000-0002-9637-8475