Elevated CO2 Induces Biochemical and Ultrastructural Changes in Leaves of the C4 Cereal Sorghum

By J. Watling, M. Press, W. P. Quick. 2000

135 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/986d6d787441f476330f32b9af3e55ea1652916a

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Citations in the corpus

The C4 pathway: an efficient CO2 pump (2004, background): “Cell wall width varied between 0.13 and 0.66 µm with an average width of 0.36 µm. Measurements from micrographs of Hattersley and Browning (1981) range from 0.24 to 1.4 µm. Watling et al. (2000) found much thicker walls in Sorghum bicolor, between 1.5 and 3.6 µm. Liu and Dengler (1994) show a bund”
Canopy photosynthesis, evapotranspiration, leaf nitrogen, and transcription profiles of maize in response to CO2 enrichment (2006, background): “K I M et al. r 2006 Blackwell Publishing Ltd, Global Change Biology, 12, 588–600 plants grown at elevated Ca (see also Maroco et al., 1999; Watling et al., 2000).”
Quo vadis C4? An ecophysiological perspective on global change and the future of C4 plants (2004, background): “the initial slope and CO2-saturated A (Figure 5; Tissue et al. 1995; LeCain and Morgan 1998; Ghannoum et al. 2000; Watling et al. 2000; Snowdon et al. 2002).”
Temperature dependence of growth, development, and photosynthesis in maize under elevated CO2 (2007, background): “Photosynthetic acclimation to long-term CO2 enrichment also has been reported in C4 plants (Kim et al., 2006; Maroco et al., 1999; Read et al., 1997; Watling et al., 2000 ).”
Up-regulation of photosynthesis and sucrose metabolism enzymes in young expanding leaves of sugarcane under elevated growth CO2 (2006, background): “Sorghum plants grown at double-ambient [CO2] in controlled environment chambers (12-h photoperiod at 800 mmol m 2 s 1 PPFD) have a 49% reduction in leaf PEPC protein concentration, but no change in Rubisco protein content [29].”