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Figure 1.

Shoot growth performance of the four barley genotypes (CM72, Gairdner, XZ16 and XZ169) under normal, moderate and high salinity conditions.

(A) shoot dry weight (g−1 plant) at 35 days after salinity treatments and normal conditions (four biological replicates, bars show SE), * and ** indicates significant (P<0.05) and highly significant difference (P<0.01), respectively; (B) shoot relative dry weight (%) at 35 days after moderate (150 mM NaCl) and high (300 mM) salinity treatment; (C) pictures of shoot-plants of CM72, Gairdner, XZ16 and XZ169 at 35 days after salinity treatment and normal conditions.

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Figure 1 Expand

Figure 2.

The chlorophyll content (SPAD value) of the four barley genotypes (CM72, Gairdner, XZ16 and XZ169) at 35 days after salinity treatment and normal conditions (eight biological replicates, bars show SE).

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Figure 3.

Principal component analysis (PCA) of metabolic profiles in roots and leaves of CM72 and XZ16 under control and high salinity conditions (six biological replicates).

(A) PCA in roots; (B) PCA in leaves. CK: control; T: salt treatment; PC1, the first principal component; PC2, the second principal component.

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Figure 3 Expand

Figure 4.

Global comparison of metabolic profiles in roots and leaves between CM72 and XZ16 under control and high salinity conditions.

There are eighty-two metabolites identified in this study and the numbers in the figure indicate the numbers of metabolites with no significant difference in their contents for each comparison.

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Figure 4 Expand

Table 1.

Relative concentration and fold changes of major metabolites in roots of CM72 and XZ16 after 21 days of 300 mM salinity treatment.

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Table 1 Expand

Table 2.

Relative concentration and fold changes of major metabolites in leaves of CM72 and XZ16 after 21 days of 300 mM salinity treatment.

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Figure 5.

Change in metabolites of the metabolic pathways in roots of CM72 and XZ16 after 21 days of salinity treatment.

Numbers 1–4 on the X-axis indicate CM72-control, CM72-salt treatment, XZ16-control and XZ16-salt treatment, respectively. The concentration of metabolites on the Y-axis is presented as normalized values transformed by Metaboanalyst software (www.metaboanalyst.ca/), and the box plots show centered means and standard deviation of each variable. Metabolites in red indicate significant (P<0.05) up-accumulation in both CM72 and XZ16, in purple mean significant (P<0.05) up-accumulation in CM72 or XZ16, in light blue show significant (P<0.05) down-accumulation in CM72 or XZ16, and in dark blue represent significant (P<0.05) down-accumulation in CM72 and XZ16.

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Figure 6.

Change in metabolites of the metabolic pathways in leaves of CM72 and XZ16 after 21 days of salinity treatment.

Numbers 1–4 on the X-axis indicate CM72-control, CM72-salt treatment, XZ16-control and XZ16-salt treatment, respectively. The concentration of metabolites on the Y-axis is presented as normalized values transformed by Metaboanalyst software (www.metaboanalyst.ca/), and the box plots show centered means and standard deviation of each variable. Metabolites in red indicate significant (P<0.05) up-accumulation in both CM72 and XZ16, in purple mean significant (P<0.05) up-accumulation in CM72 or XZ16, in light blue show significant (P<0.05) down-accumulation in CM72 or XZ16, and in dark blue represent significant (P<0.05) down-accumulation in CM72 and XZ16.

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Figure 6 Expand