312 related articles for article (PubMed ID: 22139428)
1. Effects of low atmospheric CO2 and elevated temperature during growth on the gas exchange responses of C3, C3-C4 intermediate, and C4 species from three evolutionary lineages of C4 photosynthesis.
Vogan PJ; Sage RF
Oecologia; 2012 Jun; 169(2):341-52. PubMed ID: 22139428
[TBL] [Abstract][Full Text] [Related]
2. Increasing water use efficiency along the C3 to C4 evolutionary pathway: a stomatal optimization perspective.
Way DA; Katul GG; Manzoni S; Vico G
J Exp Bot; 2014 Jul; 65(13):3683-93. PubMed ID: 24860185
[TBL] [Abstract][Full Text] [Related]
3. Is C4 photosynthesis less phenotypically plastic than C3 photosynthesis?
Sage RF; McKown AD
J Exp Bot; 2006; 57(2):303-17. PubMed ID: 16364950
[TBL] [Abstract][Full Text] [Related]
4. C2 photosynthesis generates about 3-fold elevated leaf CO2 levels in the C3-C4 intermediate species Flaveria pubescens.
Keerberg O; Pärnik T; Ivanova H; Bassüner B; Bauwe H
J Exp Bot; 2014 Jul; 65(13):3649-56. PubMed ID: 24916069
[TBL] [Abstract][Full Text] [Related]
5. Growth of the C4 dicot Flaveria bidentis: photosynthetic acclimation to low light through shifts in leaf anatomy and biochemistry.
Pengelly JJ; Sirault XR; Tazoe Y; Evans JR; Furbank RT; von Caemmerer S
J Exp Bot; 2010 Sep; 61(14):4109-22. PubMed ID: 20693408
[TBL] [Abstract][Full Text] [Related]
6. Photosynthesis of C3, C3-C4, and C4 grasses at glacial CO2.
Pinto H; Sharwood RE; Tissue DT; Ghannoum O
J Exp Bot; 2014 Jul; 65(13):3669-81. PubMed ID: 24723409
[TBL] [Abstract][Full Text] [Related]
7. Does long-term cultivation of saplings under elevated CO2 concentration influence their photosynthetic response to temperature?
Šigut L; Holišová P; Klem K; Šprtová M; Calfapietra C; Marek MV; Špunda V; Urban O
Ann Bot; 2015 Nov; 116(6):929-39. PubMed ID: 25851132
[TBL] [Abstract][Full Text] [Related]
8. The temperature response of C(3) and C(4) photosynthesis.
Sage RF; Kubien DS
Plant Cell Environ; 2007 Sep; 30(9):1086-106. PubMed ID: 17661749
[TBL] [Abstract][Full Text] [Related]
9. Initial events during the evolution of C4 photosynthesis in C3 species of Flaveria.
Sage TL; Busch FA; Johnson DC; Friesen PC; Stinson CR; Stata M; Sultmanis S; Rahman BA; Rawsthorne S; Sage RF
Plant Physiol; 2013 Nov; 163(3):1266-76. PubMed ID: 24064930
[TBL] [Abstract][Full Text] [Related]
10. Antisense reduction of NADP-malic enzyme in Flaveria bidentis reduces flow of CO2 through the C4 cycle.
Pengelly JJ; Tan J; Furbank RT; von Caemmerer S
Plant Physiol; 2012 Oct; 160(2):1070-80. PubMed ID: 22846191
[TBL] [Abstract][Full Text] [Related]
11. The functional significance of C3-C4 intermediate traits in Heliotropium L. (Boraginaceae): gas exchange perspectives.
Vogan PJ; Frohlich MW; Sage RF
Plant Cell Environ; 2007 Oct; 30(10):1337-45. PubMed ID: 17727423
[TBL] [Abstract][Full Text] [Related]
12. Carbon dioxide diffusion across stomata and mesophyll and photo-biochemical processes as affected by growth CO2 and phosphorus nutrition in cotton.
Singh SK; Badgujar G; Reddy VR; Fleisher DH; Bunce JA
J Plant Physiol; 2013 Jun; 170(9):801-13. PubMed ID: 23384758
[TBL] [Abstract][Full Text] [Related]
13. Panicum milioides (C(3)-C(4)) does not have improved water or nitrogen economies relative to C(3) and C(4) congeners exposed to industrial-age climate change.
Pinto H; Tissue DT; Ghannoum O
J Exp Bot; 2011 May; 62(9):3223-34. PubMed ID: 21307386
[TBL] [Abstract][Full Text] [Related]
14. The temperature response of CO2 assimilation, photochemical activities and Rubisco activation in Camelina sativa, a potential bioenergy crop with limited capacity for acclimation to heat stress.
Carmo-Silva AE; Salvucci ME
Planta; 2012 Nov; 236(5):1433-45. PubMed ID: 22733425
[TBL] [Abstract][Full Text] [Related]
15. Photosynthesis-related characteristics of the midrib and the interveinal lamina in leaves of the C3-CAM intermediate plant Mesembryanthemum crystallinum.
Kuźniak E; Kornas A; Kaźmierczak A; Rozpądek P; Nosek M; Kocurek M; Zellnig G; Müller M; Miszalski Z
Ann Bot; 2016 Jun; 117(7):1141-51. PubMed ID: 27091507
[TBL] [Abstract][Full Text] [Related]
16. Photosynthetic responses to heat treatments at different temperatures and following recovery in grapevine (Vitis amurensis L.) leaves.
Luo HB; Ma L; Xi HF; Duan W; Li SH; Loescher W; Wang JF; Wang LJ
PLoS One; 2011; 6(8):e23033. PubMed ID: 21887227
[TBL] [Abstract][Full Text] [Related]
17. Evolution of C4 photosynthesis in the genus Flaveria: how many and which genes does it take to make C4?
Gowik U; Bräutigam A; Weber KL; Weber AP; Westhoff P
Plant Cell; 2011 Jun; 23(6):2087-105. PubMed ID: 21705644
[TBL] [Abstract][Full Text] [Related]
18. Modelling (18)O2 and (16)O2 unidirectional fluxes in plants. III: fitting of experimental data by a simple model.
André MJ
Biosystems; 2013 Aug; 113(2):104-14. PubMed ID: 23153764
[TBL] [Abstract][Full Text] [Related]
19. Photosynthetic downregulation in leaves of the Japanese white birch grown under elevated CO(2) concentration does not change their temperature-dependent susceptibility to photoinhibition.
Komatsu M; Tobita H; Watanabe M; Yazaki K; Koike T; Kitao M
Physiol Plant; 2013 Feb; 147(2):159-68. PubMed ID: 22607385
[TBL] [Abstract][Full Text] [Related]
20. Photosynthetic characterization of Rubisco transplantomic lines reveals alterations on photochemistry and mesophyll conductance.
Galmés J; Perdomo JA; Flexas J; Whitney SM
Photosynth Res; 2013 Jul; 115(2-3):153-66. PubMed ID: 23703453
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
