JXB Advance Access originally published online on February 26, 2009
Journal of Experimental Botany 2009 60(6):1633-1644; doi:10.1093/jxb/erp028
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© 2009 The Author(s).
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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RESEARCH PAPER |
Water and nitrogen conditions affect the relationships of 
13C and 18O to gas exchange and growth in durum wheat
1Unitat de Fisiologia Vegetal, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain
2International Maize and Wheat Improvement Center (CIMMYT), El Batán, Mexico
* To whom correspondence should be addressed. E-mail: j.araus{at}cgiar.org
Received 4 October 2008; Revised 5 January 2009 Accepted 26 January 2009
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Abstract |
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Whereas the effects of water and nitrogen (N) on plant
13C have been reported previously, these factors have scarcely been studied for 18O. Here the combined effect of different water and N regimes on 13C, 18O, gas exchange, water-use efficiency (WUE), and growth of four genotypes of durum wheat [Triticum turgidum L. ssp. durum (Desf.) Husn.] cultured in pots was studied. Water and N supply significantly increased plant growth. However, a reduction in water supply did not lead to a significant decrease in gas exchange parameters, and consequently 13C was only slightly modified by water input. Conversely, N fertilizer significantly decreased 13C. On the other hand, water supply decreased 18O values, whereas N did not affect this parameter. 18O variation was mainly determined by the amount of transpired water throughout plant growth (Tcum), whereas 13C variation was explained in part by a combination of leaf N and stomatal conductance (gs). Even though the four genotypes showed significant differences in cumulative transpiration rates and biomass, this was not translated into significant differences in 18Os. However, genotypic differences in 13C were observed. Moreover, 
80% of the variation in biomass across growing conditions and genotypes was explained by a combination of both isotopes, with 18O alone accounting for 50%. This illustrates the usefulness of combining 18O and 13C in order to assess differences in plant growth and total transpiration, and also to provide a time-integrated record of the photosynthetic and evaporative performance of the plant during the course of crop growth.
Key words:
13C and 18O, leaf gas exchange, water and nitrogen limitation, wheat, WUE
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Introduction |
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TopAbstractIntroductionMaterials and methodsResultsDiscussionSupplementary dataReferences |
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In recent decades, stable carbon and oxygen isotopes have been shown to be powerful non-invasive probes for characterizing photosynthetic metabolism in plants. It has been known for some time that the carbon isotope composition of plant dry matter (
13C), which is frequently expressed as the discrimination value (13C), provides a time-integrated measurement of the plant's transpiration efficiency (i.e. the ratio of carbon gain to water transpired) over the period during which dry matter is assimilated. Indeed, it is >20 years since 13C was first proposed as a potential tool for screening wheat genotypes with higher transpiration efficiency (Farquhar and Richards, 1984; Rebetzke et al., 2002), and the first genotypes selected using this approach were subsequently released in Australia (Rebetzke et al., 2002; Condon et al., 2004). Whereas increased water input has been widely reported to have a positive effect on 13C (Araus et al., 2003; Condon et al., 2004), there are contradictory reports as to how the amount of nitrogen (N) fertilization affects 13C. Thus, for wheat and other cereals, 13C has been reported to increase (Shangguan et al., 2000), decrease (Choi et al., 2005; Cabrera-Bosquet et al., 2007; Zhao et al., 2007; Serret et al., 2008), or not be affected (Hubick, 1990; White et al., 1990) as a result of N supply.
The oxygen isotope composition (18O) of organic matter is known to reflect variation in: (i) the isotopic composition of source water; (ii) evaporative enrichment in leaves due to transpiration; and (iii) biochemical fractionation during synthesis of organic matter (Craig and Gordon, 1965; Dongmann et al., 1974; Yakir, 1992; Farquhar and Lloyd, 1993). Hence, the oxygen isotope signature of plant matter, expressed either as composition (18O) or as enrichment above source water (18O), has been used to assess the leaf evaporative conditions at the time the material was formed (Yakir et al., 1990; Yakir, 1992; Saurer et al., 1997; Barbour et al., 2000a, b; Barbour, 2007). The leaf oxygen isotope signature has been negatively correlated with relative humidity (Saurer et al., 1997; Barbour et al., 2000b; Ferrio et al., 2007) and also with transpiration rate (Barbour and Farquhar, 2000; Barbour et al., 2000a). Conversely, Sheshshayee et al. (2005) reported a positive relationship between 18O and the transpiration rate in groundnut and rice genotypes that contrasts with the present theory. Moreover, Barbour et al. (2000a) have proposed the use of the stable oxygen isotope signature (in their study expressed as 18O) measured in plant matter as an integrative indicator of genetic differences in stomatal conductance (gs), as well as a predictor of grain yield in field-grown wheat. Therefore, the 18O signature of plant tissue is of interest in terms of breeding for improved water use, and genotypic variability for this trait has been identified in bread wheat (Barbour et al., 2000a; Farquhar et al., 2007; Ferrio et al., 2007). As plant material has been shown to record leaf evaporative conditions, measurement of the 18O signature might provide a powerful tool for plant breeders (Barbour, 2007), to track genotypic differences not only in stomatal conductance but also in yield. However, up to now, most studies dealing with the use of 18O for breeding have been conducted under well-watered conditions (Barbour et al., 2000 a, b; Bindumadhava et al., 2005; Sheshshayee et al., 2005), even if the plants in question have been grown under different evaporative demand (Barbour and Farquhar, 2000; Bindumadhava et al., 2006). Research involving the 18O signature under water-limited conditions is far scarcer (Yakir et al., 1990; Ferrio et al., 2007), although genotypic differences have been identified. Furthermore, the combined effect of N fertilizer and water regime on the 18O oxygen isotope composition of plant material has not been assessed, despite the fact that the amount of N fertilization may affect the photosynthetic (Lawlor, 2001) and transpiration rates (Claus et al., 1993) in wheat and other cereals.
In terms of surface area, cereals are the main crops in the Mediterranean basin, occupying preferably the dry lands. Among cereals, durum wheat is the most widely grown in the South Mediterranean basin and is a very important crop in the European agro-food industry. In these environments, water limitation, which is frequently accompanied by low N availability, is the main constraint on wheat yield (Oweis et al., 1998; Araus et al., 2002; Passioura, 2002). Selecting genotypes better suited to the lack of water (Condon et al., 2004) and N (Hirel et al., 2007) is therefore one of the main targets for increasing yield in these environments. The use of physiological traits such as phenotypical criteria for selecting genotypes better adapted to such growing conditions might help plant breeders (Bänziger et al., 2000; Araus et al., 2002; Lafitte et al., 2003). The best potential traits to use provide time-integrated (i.e. through the crop cycle) information on plant performance (Araus et al., 2002). Among these traits the signature of the stable carbon and oxygen isotopes in plant matter reflects the photosynthetic (Farquhar et al., 1989) and transpirative (Barbour 2007; Farquhar et al., 2007) conditions in which the plants were grown (Araus et al., 1998, 2003).
The aim of the present research was to study the combined effect of different water and N regimes on 13C, 18O, water-use efficiency (WUE), and growth of four contrasting genotypes of durum wheat. The usefulness of combining 13C and 18O measurements in shoot dry matter to track differences in WUE, leaf gas exchange, cumulative transpiration, and growth in these plants was also tested.
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Materials and methods |
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TopAbstractIntroductionMaterials and methodsResultsDiscussionSupplementary dataReferences |
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Plant material and growth conditions
Three durum wheat [Triticum turgidum L. ssp. durum (Desf.) Husn.] genotypes (Bicrecham-1, Lahn/Haucan, and Omrabi-3) released by the CIMMYT/ICARDA durum wheat breeding programme, plus one of the most cultivated Spanish varieties (Mexa) were grown in a greenhouse at the University of Barcelona, from December 2004 to April 2005. These four genotypes were chosen on the basis of their contrasting yield performance under Mediterranean conditions (Villegas et al., 2001; Ferrio et al., 2005). Fourteen seeds of each genotype were planted per pot (5.0 L, filled with washed sand). After germination, they were thinned to seven plants per pot, representing a plant density of
223 plants m–2, and watered daily with deionized water for 2 weeks. After this, three different water regimes and two N levels were imposed, by applying nutrient solution every 2 d. The water levels were achieved by weighing the pots prior to watering, and then adding the amount of water needed to reach 40, 70, and 100% of their container capacity (CC). The N supply was controlled using two different nutrient solutions: complete Hoagland solution (Hoagland and Arnon, 1950) and the same solution with N diluted four times (i.e. 0.06725 g N L–1 and 0.27 g N L–1 for the low and high N, respectively). Pots with different treatments were displayed in a randomized complete block design. Each treatment was replicated four times and the whole experimental set-up accounted for a total of 96 pots. Plants were grown in the greenhouse under mean day/night temperatures of 25/15 °C, a maximum photosynthetic photon flux density (PPFD) of 1000 µmol m–2 s–1, and a mean vapour pressure deficit (VPD) of 0.75 kPa.
Leaf gas exchange measurements
Gas exchange of the flag leaf blade was measured 2 weeks after anthesis, just before harvesting, using an open IRGA LI-COR 6400 system (LI-COR Inc., Lincoln, NE, USA). Photosynthetic measurements were performed under light-saturated conditions (1000 µmol photon m–2 s–1 of PPFD), at 25 °C and 400 µmol mol–1 of CO2. The measured gas exchange parameters were: light-saturated net CO2 assimilation rate (Asat); transpiration rate (E); and stomatal conductance (gs). Then the ratio of intercellular to ambient CO2 concentration (Ci/Ca) was calculated according to Sharkey and Raschke (1981).
Determination of cumulative transpiration and water status
The amount of water evapotranspired was monitored throughout the experiment by weighing each pot just prior to watering. The pots were then adjusted to their water regime (40, 70, and 100% CC) by adding nutrient solution to maintain the experimental design. Simultaneously, empty pots without plants were also weighed to record direct evaporation from the soil. Then, the cumulative transpiration (Tcum) was calculated as the difference between evapotranspiration and evaporation.
Water status was determined by means of measurements on relative water content (RWC) in the flag leaf blades 1 d after the last watering and just before harvesting. Leaf blade segments were weighed (fresh weight; FW), floated on distilled water at 4 °C overnight, and weighed again (TW). They were then dried at 80 °C for 48 h. After this, the dry weight (DW) was determined. RWC was then calculated as:
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Water-use efficiency
WUE was calculated using both instantaneous and time-integrated measurements. The time-integrated WUE, WUEbiomass, was calculated as the ratio of total aboveground biomass (AB) to evapotranspired water throughout plant growth. Moreover, instantaneous WUE (WUEinstantaneous) and intrinsic WUE (WUEintrinsic) were calculated as the ratio of Asat to E and gs, respectively.
Total nitrogen content and carbon isotope analyses
For each analysis, 1 mg of fine powdered shoot, spike, flag leaf, or root tissue was weighed in tin cups. The total N content of samples was analysed at the Colorado Plateau Stable Isotope Laboratory (CPSIL) using an Elemental Analyser (EA) (Carlo Erba 2100, Milan, Italy). The same EA interfaced with an isotope ratio mass spectrometer (IRMS) (Thermo-Finnigan Deltaplus Advantage, Bremen, Germany) was also used to analyse 13C/12C ratios (R) of plant material. Results were expressed as 13C values, using a secondary standard calibrated against Vienna Pee Dee Belemnite calcium carbonate (VPDB), and the analytical precision was 0.1
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The carbon isotope discrimination (13C) of plant parts was then calculated from a and p (Farquhar et al., 1989) as:
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13C=–11.3.
Oxygen isotope analyses
The oxygen isotope composition was determined in shoots (including leaves and stems), since this plant part was considered as the most representative because it makes up a significant proportion of the dry weight in the plant. In addition, 13C of shoots integrates the photosynthetic performance and the water status of the plant during their growth better than other plant parts (Tambussi et al., 2007a).
The 18O/16O ratios of irrigation water were determined by the CO2:H2O equilibration technique and using an IRMS (Delta S Finnigan MAT, Bremen, Germany). The 18O/16O ratios of shoot dry matter were determined by an on-line pyrolysis technique using a thermo-chemical elemental analyser (TC/EA Thermo Quest Finnigan, Bremen, Germany) coupled with an IRMS (Delta C Finnigan MAT, Bremen, Germany). Results were expressed as 18O values, using a secondary standard calibrated against the Vienna standard mean oceanic water (VSMOW), and the analytical precision was 0.2.
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Then, following the same notation used for carbon isotope discrimination, the 18O enrichment in shoot parts (18Os) was calculated as follows:
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18Os and 18Oiw refer to the oxygen isotope compositions of shoots and irrigation water, respectively (18Oiw was approximately –6.5.). The 18O/16O ratios of both irrigation water and shoot dry matter were calculated at the Scientific Facilities of the University of Barcelona.
Biomass determination
Total biomass was collected 2 weeks after anthesis. The spike, flag leaf, the rest of the shoot (including leaves and stems), and the root were separated and oven-dried at 80 °C for 48 h, before being weighed and powdered. The leaf dry mass per unit leaf area (LDM) of the flag leaf blades was calculated as the ratio between dry weight and leaf surface (g m–2). Moreover, the specific leaf nitrogen (SLN) of the flag leaf blades was calculated as the ratio between dry N content in dry matter and the leaf surface (g m–2).
Statistical analysis
Analysis of variance (ANOVA) was performed using the General Linear Model procedure to calculate the effects of water and genotype within each N treatment. Means were compared using a Tukey-b multiple comparison test (P <0.05). The bivariate correlation procedure was used to calculate the Pearson correlation coefficients. Multiple linear regression analysis (stepwise) was used to analyse the relationship between the variables studied. Linear stepwise models were built from water and genotype means within each N treatment. Data were analysed using the SPSS statistical package (SPSS Inc., Chicago, IL, USA).
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Results |
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Plant growth and N content
Large differences in total AB and root biomass, as well as in the different components of AB, were observed in response to the different levels of water supply and N fertilization studied (Table 1, Fig. 1). Accumulated transpiration (Tcum) also changed greatly in response to both N and water treatments (Table 1). Thus, AB, spike biomass (SB), and Tcum in control plants (i.e. high N and 100% CC) were five, three, and three times higher, respectively, than in plants grown under the most limiting conditions (i.e. low N and 40% CC, Table 1). However, the effect of water regime was greater in the low than in the high N regime; in fact, there were two-way significant interactions between water regime and N levels for total AB, SB, and Tcum. In addition, large genotypic differences in these three traits were also observed. Omrabi-3 was the genotype with highest AB and Tcum in both N treatments, whilst Mexa had the lowest values. Bicrecham-1 and Lahn/Haucan had intermediate values (Table 1). However, whereas interactions of genotypes with both N and water conditions were not significant for Tcum, these interactions did reach significance for total biomass, although only between genotypes and N regime. LDM values were affected by genotype but not by water regime and N, and the only significant interaction was between genotype and water regime.
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The results also showed that the N content of shoots on a dry matter basis (SN), as well as that of the flag leaf per unit leaf area (SLN) and dry weight (LN), increased in response to N supply and, to a lesser extent, as water increased (Table 1). In addition, genotypic differences in the N content of shoots and the flag leaf were found. In both N treatments, Omrabi-3 was the genotype with the highest SLN and LN in the flag leaf, whereas Mexa had the lowest values. SN was also the highest and the lowest in Omrabi-3 and Mexa, respectively, but only under high N conditions. In fact, SN showed a genotypic interaction between genotype and both water and N treatments, whereas LN did not show any interactions between genotypes and growing conditions; for SLN, only interactions between genotype and water regime were observed (Table 1).
Leaf gas exchange
Water supply had a significant positive effect on light-saturated net CO2 assimilation (Asat) but not on stomatal conductance (gs) or transpiration (E). However, for all three parameters there was a significant interaction between water regime and N levels. Thus, Asat, gs, and E increased (28, 52, and 38%, respectively) with water supply under high N treatments, whereas no differences were found in plants grown with a low N supply (Table 1). The Ci/Ca ratio did not change significantly in response to water treatment or according to the N regime. The N regime did have a significant effect on the four gas exchange parameters shown in Table 1. Hence, higher values of Asat, gs, Ci/Ca, and E were found in the low N compared with the high N treatment. Genotypic differences for Asat and Ci/Ca were observed, but, whereas the interaction between genotype and water regime was not significant, that between genotype and N regime was. Thus, at low N, Omrabi-3 showed higher values of Asat compared with the other three genotypes, while at high N no differences between the four genotypes were observed. Conversely, for Ci/Ca, Omrabi-3 showed lower values than the other genotypes at high N, while no differences were observed at low N. Differences across treatments and genotypes in net photosynthesis were mediated mostly by differences in stomatal conductance, as shown by the relationship between Asat and gs when all the treatments were plotted together (Fig. 2a). In contrast, Asat and LN were only significantly correlated at low N (Fig. 2b).
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Water status and WUE
Water supply increased the RWC values in both N treatments, although significant differences between water treatments were only found in plants grown at low N (Table 1). However, these values remained relatively high (>85%) even in the lower water regime. The N regime did not affect RWC. WUE, measured both gravimetrically (WUEbiomass) and using gas exchange measurements (WUEintrinsic and WUEinstantaneous), increased in response to N fertilization (Table 2). However, the effect of water deficit on these parameters was not clear. While at low N the three traits showed the same pattern of increase as the water supply increased, only the response of WUEbiomass reached significance. At high N, an increase in water supply only led to a significant decrease in WUEintrinsic, and, in fact, significant interactions between water and N conditions were observed for WUEbiomass and WUEintrinsic. Furthermore, significant differences between genotypes were also observed for all three WUEs, particularly in plants grown at high N. Nevertheless, Omrabi-3 was the most efficient genotype in terms of water use, regardless of the N regime.
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Effects of water and nitrogen on
13C and 18OsN conditions and genotype had a significant effect on
13C, whereas water had no effect (except for 13C of flag leaves). When the two N treatments were compared, higher 13C values in plant dry matter were found in low N plants (Table 2). Moreover, a slight but significant increase in 13C of all plant parts was observed with increasing water supply from 70% to 100% CC in plants grown under high N, while, under low N, 13C values from 70% to 100% CC followed the opposite pattern. In fact, the two-way interactions between growing conditions were significant for all the 13C. In addition, significant genotypic differences in 13C were found in all plant organs within each N and water treatment. The Mexa genotype showed the highest values of 13C, regardless of the N regime and the tissue considered, whereas Omrabi-3 showed the lowest values but only at high N. In fact, there was a significant interaction between genotype and N regime for the four different 13C analysed. In addition, differences in 13C between plant parts were also found (Table 2).
The 18O of shoots was enriched compared with the 18O of irrigation water (–6.5) and, therefore, 18Os was positive in all cases (Table 2). The water regime had a significant effect on 18Os, whilst no differences in 18Os values were found when comparing genotypes or N treatments. Thus, within each N treatment, 18Os decreased as the water supply increased. Moreover, two-way interactions were not significant in any case.
Relationships between different traits
When data for all the water regimes and genotypes grown together at high N were combined, 13C of shoots, flag leaves, spikes, and roots correlated strongly and negatively with time-integrated WUE, and also negatively with instantaneous measurements of WUE (Table 3). Under low N conditions, correlations of different 13C only reached significance against WUEintrinsic, with 13C of spikes being the best correlated. In contrast, the results showed no significant correlations between 18O of shoots and either instantaneous or time-integrated measurements of WUE in either of the N treatments (Table 3). In addition, 18O of shoots did not significantly correlate with 13C of shoots, regardless of the N regime considered (data not shown).
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Due to the water regime increasing biomass and decreasing
18Os values, significant negative correlations were found between 18Os and either AB, SB, or Tcum in both N treatments (Table 4; Fig. 4). Conversely, 13Cs did not correlate with either Tcum or AB (Table 4). However, it did correlate positively with SB, although only in the high N treatment.
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Furthermore, whereas at high N
13Cs correlated positively with gs and E, 18Os correlated negatively with these same gas exchange parameters; these correlations were not found in the low N treatments. Moreover, in the high N treatments, strong correlations were found between the ratio of carbon and oxygen isotopes (13Cs/18Os) and gs and E (Table 4; Fig. 5).
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In addition, a stepwise analysis was performed to explain the causes of variation of the different parameters studied (Table 5). Thus, the variation in the total AB was explained in both N treatments by the combination of
18Os and 13Cs. 18Os and 13C explained, respectively, 59% and 17% of the variation in AB at low N, while under high N 18Os and 13C explained 48% and 36% of AB variation, respectively. Moreover, in both N treatments, variation in 18Os was mainly explained by changes in Tcum. On the other hand, 13Cs and Asat variations were explained in both N treatments by a combination of gs and leaf N (expressed as LN or SLN). Differences in the ratio Ci/Ca were explained in the high N treatments by changes in gs and leaf N, whereas no explanation was found for low N treatments when these variables were entered into the model.
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Discussion |
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TopAbstractIntroductionMaterials and methodsResultsDiscussionSupplementary dataReferences |
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Water and nitrogen effects on plant growth and water status
Although the different water regimes produced large differences in biomass in both N treatments (Fig. 1), the relatively small decreases in gas exchange parameters,
13C and RWC, suggest that mild water stress was experienced even with the most water-limited treatments. This can be explained in part by a combination of different factors, including the fact that plant growth, more than gas exchange, is affected by moderate water stress (Hsiao, 1973; Jones, 1980; McCree, 1986; Kramer and Boyer, 1995). Hence, both the way in which water regimes were imposed (i.e. sustained water limitation during the course of crop growth) and the growing conditions in pots led plants to acclimatize, with an adjustment of the total leaf area to the available water conditions in the pot and, therefore, with water status (e.g. gs and RWC) remaining at moderate or non-water stress levels. Moreover, the lack of differences in LDM between water treatments (and therefore the absence of differences in leaf structure) reinforces the idea that plants adjust their total leaf area to water availability.
In addition, when both N treatments were compared, a negative effect of N supply on gas exchange parameters was observed. High N supply clearly increased the total plant biomass (and therefore the total leaf area), thereby causing leaves to compete for the available water in the pot. This resulted in a negative effect on gas exchange parameters (mainly in terms of decreasing gs) in both well-watered and water-limited plants (in which the effect was greater, Table 1). Genotypic differences may also support this situation, as in the case of Omrabi-3, where the large increase in biomass reached in the high N treatment resulted in a clear decrease in gs and E values. Similar results were found in field-grown rice in aerobic soils (Kondo et al., 2004), where a large biomass production due to high N fertilization exacerbated water stress, which resulted in lower stomatal conductance and 13C.
Source of variation on plant isotope signatures
Carbon isotope discrimination (13C) varied extensively between the different analysed plant parts (shoots, flags, spikes, and roots), as predicted by both theory (Hubick and Farquhar, 1989; Badeck et al., 2005) and previous results reported in wheat grown under Mediterranean conditions (Araus et al., 1997; Merah et al., 2002). Lower 13C values in spikes compared with the shoot or flag leaf may reflect changes in soil water availability, as well as the increase in evaporative demand occurring during the final stages of crop growth (Condon and Richards, 1992); however, the lower gs of the spike compared with that of leaves (Araus et al., 1993; Tambussi et al., 2005, 2007b) may also be involved.
Moreover, when N treatments were compared, a significant decrease in 13C values in plants grown under high N supply was found. According to Farquhar et al. (1989), a decrease in 13C can be explained by a reduction in the ratio Ci/Ca (Table 1). This reduction in Ci/Ca may be due to either greater photosynthetic capacity or lower gs, or to both factors (Farquhar and Richards, 1984; Condon et al., 2004). Although many reports have suggested that N fertilization may decrease 13C by lowering Ci/Ca, mainly as a result of improved carboxylation efficiency (Livingstone et al., 1999; Ripullone et al., 2004), a significant decrease in Asat in response to N fertilization was found. This can be explained by the lower gs values found in the high N treatments, which resulted in a significant decrease in both Asat and 13C as compared with the low N treatments.
However, within each N treatment, and regardless of differences found between N treatments, the increase in Asat was associated with increases in gs and LN (as revealed by stepwise analysis, Table 5). Nevertheless, the effect of LN was higher under low N treatments. Hence, at low N, where the effect of gs was lower, a higher N content in leaves (SLN and LN) associated with more water input and/or N application was probably involved in lowering Ci/Ca and 13C. Conversely, at high N, differences in Asat were mainly associated with changes in gs. This is supported by the close relationships found between Asat and gs and LN (Fig. 2).
It was also observed that 18Os increased significantly in the water-limited treatments, while no differences in 18Os were found between N treatments. A similar pattern in response to differences in water status was found in bread wheat kernels (Ferrio et al., 2007), where plants with the wettest conditions had the lower 18O values. Similarly, Saurer et al. (1997) reported a variation in 18O in the cellulose of trees grown under different soil moisture conditions, with the lowest values in those species growing with the highest moisture soil index.
Even though the four genotypes showed significant differences in cumulative transpiration rates, this was not translated into significant differences in 18Os between genotypes. Nevertheless, there are reports showing genotypic variability for this trait in bread wheat (Barbour et al., 2000a; Ferrio et al., 2007). However, a negative trend was observed, with higher 18O enrichment in those genotypes with lower transpiration rates when grown at high N.
Stepwise analysis revealed that variation in 18Os was explained in both N treatments as a response to Tcum. In accordance with the theory (Barbour and Farquhar, 2000), where 18O in plant organic material may provide an integrated measurement of water loss, it was found that under both N treatments 18Os was able to differentiate between water treatments, becoming enriched in 18O as water supply decreased. This was also the case under low N levels, where differences between water regimes in terms of leaf gas exchange were less evident.
Although 18O clearly showed differences between water treatments, the 18O signature could be altered as shoots including leaves and stems were measured. It is well known that during cellulose formation in newly developing stems (sink tissues), the cleavage of the sucrose formed in leaves allows re-equilibration of some or all of the oxygen with the surrounding stem water (Barbour and Farquhar, 2000), altering the 18O enrichment which has already occurred in the leaves (sucrose source). However, the shoot samples contained not only stems but also a large proportion of leaves. Nevertheless, a simplified Péclet model developed by Barbour and co-workers (http://www.ecophys.biology.utah.edu/) was used to validate the results. The model reasonably predicted the measured 18Os values (r=0.69 and slope 1.1) although the range of prediction was lower than that observed (Supplementary Fig. S1 available at JXB online).
Correlation between traits
The negative correlations observed between 18Os and both gs and E are consistent with the strong relationships found between 18O and gs and E in bread wheat (Barbour et al., 2000a) and in cotton (Barbour and Farquhar, 2000). However, these results contrast with the positive relationships between 18O of leaf biomass and mean transpiration rate reported in groundnut and rice (Sheshshayee et al., 2005) and, more recently, in the tropical tree, Ficus insipida (Cernusak et al., 2007). Farquhar et al. (2007) have recently discussed the results of Sheshshayee et al. (2005) stating that when variation in E is caused by changes in the evaporative demand a positive relationship between E and isotopic enrichment can be maintained. However, when variation in E is driven by changes in gs a negative relationship between E and isotope enrichment is expected. This is the case in the present study where, at a given VPD, a lower stomatal conductance caused 18O enrichment in plant dry matter, and a negative correlation between 18Os and E was observed (Table 4). A nice example is shown in Barbour and Farquhar (2000) where at a given relative humidity cotton leaves with lower gs, and therefore lower E and higher leaf temperature, exhibited higher 18O enrichment.
Regardless of the correlations between 18O and gas exchange parameters, under the particular growing conditions of the present research, where water regimes were maintained at a constant and steady level through watering, it was found that cumulative transpiration (Tcum) played a pivotal role in 18O. Moreover, Tcum also strongly determined the amount of biomass accumulated, and this was supported by the strong positive correlations found between AB and Tcum (r=0.99, P <0.001 and r=0.99, P <0.001 for the low and high N treatments, respectively; Fig. 3). Therefore, a negative relationship between 18O and AB in both N treatments was also found (Fig. 4b, Table 4).
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In addition, and as suggested by Barbour et al. (2000a), under well-watered to mild water-limited conditions, and when grain yield and stomatal conductance are positively correlated, the 18O signature would be a good predictor of yield. In agreement with this, a positive correlation between gs and SB (r=0.87, P <0.01, data not shown) was found in the high N treatments, and therefore the expected correlation between SB and
18Os was also found (r= –0.80, P <0.01, Table 4).
Furthermore, Barbour et al. (2000a) reported that when variation in 13C is mainly driven by changes in gs, a negative correlation between 13C and 18O (or positive between 13C and 18O) is expected. Saurer et al. (1997) also reported a linear positive relationship between 13C and 18O cellulose of trees grown under different soil moisture conditions, stating the linear dependence of the ratio Ci/Ca on the ratio ea/ei. In the present results, although a negative relationship was found between 13Cs and 18Os (r= –0.42), this was not statistically significant. This can be explained by the fact that plants grown at high N supply displayed a 13C variation that was not completely attributable to changes in gs but was also influenced by intrinsic photosynthetic capacity (Table 5). As a consequence, the increase in Ci/Ca caused by increased gs will be partially offset by a decrease in Ci/Ca associated with an increased photosynthetic capacity (Barbour et al., 2000a), and therefore the expected correlation between 13C and 18O is reduced. In addition, at low N, no relationship was found between the two isotopes.
Bindumadhava et al. (2005) reported that the ratio Ci/gs can be used as a rapid estimate of ‘instantaneous’ carbon assimilatory capacity, since at a given gs the variation in Ci is mainly a function of photosynthetic capacity. Moreover, in their study, variation in 13C and 18O was mainly driven by changes in photosynthetic capacity and stomatal conductance, respectively, and therefore they reported that the ratio 13C/18O would represent a time-averaged estimate of Ci/gs, and hence an integrated estimation of the photosynthetic capacity during the course of crop growth. Conversely, the present results showed the inverse trend, with a negative correlation between the ratios Ci/gs and 13C/18O (r= –0.73, P <0.01, Fig. 5b) in the high N treatments. These opposing results can be explained through consideration of the causes affecting variation in 13C and 18O signatures. Whereas the work of Bindumadhava et al. (2005) indicated that differences in 13C were mainly driven by changes in photosynthetic capacity, the present results showed that 13Cs was associated with changes in both gs and intrinsic photosynthetic capacity. This could also explain why gs and E correlated better with 13Cs/18Os than with each isotope alone (Table 4).
In the present study, the differences in gas exchange parameters (gs and E), as well as their correlation with stable isotopes found in the high N treatments, contrast with the lack of such results in the low N treatments. In the case of the correlation between 13C and gas exchange parameters, this might be explained by 13C dependence on Ci/Ca. Thus, at low N, changes in Ci/Ca across water regimes are not as dependent on gs as at high N (see Table 5), and, in fact, increasing water input did not produce a parallel increase in gs and E or Asat. In the case of 18O, instantaneous transpiration at low N is also less clearly affected by the water regime than at high N. Conversely, cumulative transpiration is highly dependent on the total leaf area, which in turn is strongly affected by the water regime in both N treatments. Thus, at high N, more water implies not just more photosynthesis and a better water status but, probably (and more importantly), higher levels of accumulated transpiration and, therefore, higher rates of plant growth. In contrast, at low N, the effect of higher quantities of irrigation leading to increased plant growth and increased cumulative transpiration is indirect, and this is mediated by greater availability of N with increasing fertirrigation. Hence, differences obtained in terms of biomass were not paralleled by significant differences in gas exchange parameters.
In addition, the strong correlation found between 18Os and AB in both N treatments, along with the lack of correlation of AB with 13Cs, emphazise the fact that plant growth (and thus total water transpired by the plant) more than gas exchange per unit leaf area is affected by moderate and steady water stress.
Conclusion
In accordance with the current theory of Barbour and Farquhar (2000), this study shows an increase in the 18O enrichment of plant matter in water-limited plants as a consequence of a decrease in transpiration. Thus, under the particular growing conditions studied here, 18O was strongly and negatively associated with AB regardless of the N regime. In fact, 18O was the only trait among the stable isotope and gas exchange traits analysed that did not show an interaction between growing conditions and which was only affected by the water regime. This illustrates the usefulness of measuring 18O to assess differences in plant growth and total transpiration. In addition, this study showed that the two isotopes, 13C and 18O, are not mutually exclusive and that the combined measurement of both at the plant matter level may provide a time-integrated record of the photosynthetic and evaporative performance of the plant during the course of crop growth, thus helping plant breeders to select genotypes that are better adapted to water limitation, regardless of the N status.
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Supplementary data |
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TopAbstractIntroductionMaterials and methodsResultsDiscussionSupplementary dataReferences |
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Supplementary data are available at JXB online.
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Acknowledgements |
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This study was supported in part by the European research project WatNitMed (INCO CT-2004-509107) and the Spanish Ministry of Education and Science project (AGL2006-13541-C02). LC-B and GM were the recipients of a doctoral fellowship (Programa Nacional de Formación de Personal Universitario, Spanish Ministry of Education and Science).
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Abbreviations |
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AB, aboveground biomass; Asat, light-saturated net CO2 assimilation rate; Ci and Ca, intercellular and ambient CO2 concentrations;
13C, carbon isotope composition; 13C, carbon isotope discrimination; 18O, oxygen isotope composition; 18O, oxygen isotope enrichment; E, transpiration rate; gs, stomatal conductance; LDM, leaf dry mass per unit leaf area; RWC, relative water content; SB, spike biomass; WUEbiomass, time-integrated water-use efficiency; WUEinstantaneous, instantaneous water-use efficiency; WUEintrinsic, intrinsic water-use efficiency. |
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