Evidence map›Paper›PMID 24692650›Full record

ArticleJournal of experimental botany2014

Photosynthetic flexibility in maize exposed to salinity and shade.

Robert E Sharwood, Balasaheb V Sonawane, Oula Ghannoum

Open access · bronzeAbstract read
In one paragraph

Article in Journal of experimental botany, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 85 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Robert E SharwoodHawkesbury Institute for the Environment, University of Western Sydney, Richmond, Locked bag 1797, Penrith NSW 2751, Australia.
Balasaheb V SonawaneHawkesbury Institute for the Environment, University of Western Sydney, Richmond, Locked bag 1797, Penrith NSW 2751, Australia.
Oula GhannoumHawkesbury Institute for the Environment, University of Western Sydney, Richmond, Locked bag 1797, Penrith NSW 2751, Australia o.ghannoum@uws.edu.au.
Western Sydney University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

C4 photosynthesis involves a close collaboration of the C3 and C4 metabolic cycles across the mesophyll and bundle-sheath cells. This study investigated the coordination of C4 photosynthesis in maize plants subjected to two salinity (50 and 100mM NaCl) treatments and one shade (20% of full sunlight) treatment. Photosynthetic efficiency was probed by combining leaf gas-exchange measurements with carbon isotope discrimination and assaying the key carboxylases [ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) and phosphoenolpyruvate carboxylase (PEPC)] and decarboxylases [nicotinamide adenine dinucleotide phosphate malic enzyme (NADP-ME) and phosphoenolpyruvate carboxykinase (PEP-CK)] operating in maize leaves. Generally, salinity inhibited plant growth and photosynthesis to a lesser extent than shade. Salinity reduced photosynthesis primarily by reducing stomatal conductance and secondarily by equally reducing Rubisco and PEPC activities; the decarboxylases were inhibited more than the carboxylases. Salinity increased photosynthetic carbon isotope discrimination (Δp) and reduced leaf dry-matter carbon isotope composition ((13)δ) due to changes in p i/p a (intercellular to ambient CO2 partial pressure), while CO2 leakiness out of the bundle sheath (ϕ) was similar to that in control plants. Acclimation to shade was underpinned by a greater downregulation of PEPC relative to Rubisco activity, and a lesser inhibition of NADP-ME (primary decarboxylase) relative to PEP-CK (secondary decarboxylase). Shade reduced Δp and ɸ without significantly affecting leaf (13)δ or p i/p a relative to control plants. Accordingly, shade perturbed the balance between the C3 and C4 cycles during photosynthesis in maize, and demonstrated the flexible partitioning of C4 acid decarboxylation activity between NADP-ME and PEP-CK in response to the environment. This study highlights the need to improve our understanding of the links between leaf (13)δ and photosynthetic Δp, and the role of the secondary decarboxylase PEP-CK in NADP-ME plants such as maize.

Indexed as

PhotosynthesisPlant TranspirationStress, PhysiologicalCarbon DioxideCarbon IsotopesLightMalate DehydrogenaseNitrogenPhosphoenolpyruvate Carboxykinase (ATP)Phosphoenolpyruvate CarboxylasePlant ProteinsRibulose-Bisphosphate CarboxylaseSalinityZea maysCarbon DioxideCarbon IsotopesMalate Dehydrogenasemalate dehydrogenase (oxaloacetate-decarboxylating) (NADP+)NitrogenPhosphoenolpyruvate Carboxykinase (ATP)Phosphoenolpyruvate CarboxylasePlant ProteinsRibulose-Bisphosphate CarboxylaseC4 photosynthesiscarbon isotope discriminationleakinessNADP-MEPEPCPEP-CKRubisco.

Identifiers

PMID24692650
PMCPMC4085963
OpenAlexW2105219119

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.