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Helianthus Nighttime Conductance and Transpiration Respond to Soil Water But Not Nutrient Availability^1,[W],[OA]

Department of Plant Biology, University of Georgia, Athens, Georgia 30602–7271

	ABSTRACT

TOP ABSTRACT RESULTS DISCUSSION MATERIALS AND METHODS LITERATURE CITED

 
We investigated the response of Helianthus species nighttime conductance (g_night) and transpiration (E_night) to soil nutrient and water limitations in nine greenhouse studies. The studies primarily used wild Helianthus annuus, but also included a commercial and early domesticate of H. annuus and three additional wild species (Helianthus petiolaris Nutt., Helianthus deserticola Heiser, and Helianthus anomalus Blake). Well-watered plants of all species showed substantial g_night (0.023–0.225 mol m^–2 s^–1) and E_night (0.29–2.46 mmol m^–2 s^–1) measured as instantaneous gas exchange. Based on the potential for transpiration to increase mass flow of mobile nutrients to roots, we hypothesized that g_night and E_night would increase under limiting soil nutrients but found no evidence of responses in all six studies testing this. Based on known daytime responses to water limitation, we hypothesized that g_night and E_night would decrease when soil water availability was limited, and results from all four studies testing this supported our hypothesis. We also established that stomatal conductance at night was on average 5 times greater than cuticular conductance. Additionally, g_night and E_night varied nocturnally and across plant reproductive stages while remaining relatively constant as leaves aged. Our results further the ability to predict conditions under which nighttime water loss will be biologically significant and demonstrate that for Helianthus, g_night can be regulated.

Several researchers have speculated that nighttime water loss could enhance nutrient uptake by increasing mass flow of soluble nutrients to plant roots (Snyder et al., 2003; Daley and Phillips, 2006; Caird et al., 2007). The Barber-Cushman model predicts that increasing water flux to the rhizoplane minimizes or eliminates the formation of a nitrate depletion zone around plant roots when conditions are appropriate for E_night (Barber and Cushman, 1981; Barber, 1995). Empirically, McDonald et al. (2002) demonstrated a benefit of increased transpiration on nitrate delivery and uptake by Populus plants. Although the Tanner and Beevers (2001) study is sometimes cited as contrary evidence, it dealt only with effects of transpiration on long-distance nitrogen transport within the xylem, not with mass flow delivery to roots. Thus, increased nutrient acquisition may represent a benefit that counters the cost of water loss at night.

If nighttime water loss increases nutrient acquisition, then plants may benefit from the ability to regulate g_night in response to nutrient conditions. The effects of nitrate availability on g_day and E_day have been investigated and are variable (Chapin, 1990; Fredeen et al., 1991; Ciompi et al., 1996; Cechin and Fumis, 2004). Potential regulatory pathways are still being debated (Dodd et al., 2003; Sakakibara et al., 2006). Two recent field studies with nutrient addition treatments found that g_night declined in response to nutrient additions (Ludwig et al., 2006; Scholz et al., 2007). However, the experimental designs of these studies did not permit direct effects due to reduced plant demand for nutrient acquisition regulating g_night to be separated from indirect effects of plant size or water status. More studies are needed that experimentally manipulate soil nutrient availability and test its effect on g_night and E_night, independent of confounding variation in soil and plant water potential.

During the day, stomatal conductance is regulated with respect to changing soil water potential and atmospheric demand to minimize use of available water during CO₂ uptake and maintain soil-to-leaf hydraulic continuity (Sperry et al., 2002). To further optimize use of limited soil water, regulation may also occur at night, reducing g_night and consequently E_night. This expectation held true for droughted wheat plants, where g_night decreased as compared to well-watered controls (Rawson and Clarke, 1988). However, variable results have been obtained from studies that manipulated soil water potential with salt addition (Donovan et al., 1999) or through irrigation in the field (Donovan et al., 2003). At this time, generalization about the effect of soil water availability on g_night and E_night is not possible, and further examination in controlled experiments is needed.

The magnitude of g_night and E_night may also vary temporally as leaves age or across plant reproductive stages (e.g. prereproductive, reproductive). Field studies have shown that small juvenile plants have higher g_day and E_day and lower water use efficiency than larger adults (Donovan and Ehleringer, 1991, 1992). Leaf age has been shown to cause a decline in g_day in sunflowers (Helianthus annuus; Cechin and Fumis, 2004). Similar to these daytime responses, Grulke et al. (2004) found higher g_night in large saplings than in mature trees, and Blom-Zandstra et al. (1995) found g_night of rose leaves declined as leaves aged from 3 to 6 weeks. However, in both of these cases, direct effects of reproductive stage and leaf age cannot be differentiated from additional variables such as plant size and age. Controlled studies are needed to accurately assess the role of plant reproductive stage and leaf age on g_night.

Most measures of plant water loss include loss across both the cuticular and stomatal pathways operating in parallel. Because cuticular conductance (g_cuticular) is very small compared to daytime conductance through open stomata (g_stomata), its contribution to g_day has traditionally been ignored. However, when considering much lower magnitude g_night and E_night, cuticular losses may represent a substantial portion of the total measurement. Estimates of g_cuticular, ranging from 0.004 to 0.016 mol m^–2 s^–1, have been derived from gas exchange measurements of intact leaves where stomatal closure has been induced by either leaf wilting (water stress) or exogenous abscisic acid (ABA) application (Rawson and Clarke, 1988; Kerstiens, 1995; Boyer et al., 1997; Burghardt and Riederer, 2003; Nobel, 2005). These estimates include water loss through the cuticle and maximally closed stomata and thus represent a functional definition of g_cuticular. New techniques are available for estimating conductance and permeability of the cuticle separate from the stomatal pores, and they highlight the potential for variability in cuticular permeability (Schreiber et al., 2001; Santrucek et al., 2004; Kerstiens, 2006). However, it is still useful to measure water loss occurring though the cuticle plus stomata at maximal closure, because this represents a baseline that is not subject to short-term stomatal regulation.

We examined g_night and E_night in controlled greenhouse studies using wild H. annuus, H. annuus domesticates (commercial cultivar and Hopi domesticate), and a group of closely related wild species (Helianthus anomalus Blake, Helianthus deserticola Heiser, and Helianthus petiolaris Nutt.). Substantial g_night (0.08–0.10 mol m^–2 s^–1) has been reported for H. annuus and H. anomalus in their native habitats (Snyder et al., 2003; Ludwig et al., 2006). The inclusion of several species allowed us to assess whether results for regulation of g_night and E_night can be generalized across closely related species. As large annuals, the Helianthus species were easily grown in the greenhouse, allowing experimental manipulation of soil treatments under controlled environmental conditions. This allowed for robust tests of environmentally stimulated regulation and nighttime water loss at different phases of maturity.

Our objective was to investigate issues of regulation and variation in g_night and E_night. Specifically, we addressed three questions: Are g_night and E_night regulated in response to soil nutrient and water availability? Under optimal soil conditions, do g_night and E_night vary nocturnally (within a night) and across leaf lifespan and plant reproductive stage? Finally, is g_night substantially larger than g_cuticular when the latter is defined functionally as conductance though the cuticle and maximally closed stomata?

	RESULTS

TOP ABSTRACT RESULTS DISCUSSION MATERIALS AND METHODS LITERATURE CITED

 
In all nine greenhouse studies (summarized in Table I ; Supplemental Table S1), the four species of wild Helianthus plus domesticated H. annuus and H. annuus Hopi all showed substantial loss of water at night. For sufficiently watered plants, g_night averaged 0.098 mol m^–2 s^–1 (range, 0.023–0.225) and E_night averaged 1.19 mmol m^–2 s^–1 (range, 0.29–2.46). Where available, g_day averaged 0.893 mol m^–2 s^–1 and E_day averaged 15.60 mmol m^–2 s^–1. VPD_l for the gas exchange measurements averaged 1.30 kPa at night and 2.14 kPa during the day.

Six studies applied a soil nutrient treatment, four of which only manipulated soil nitrate (Table I). There was no effect of nutrient limitation on g_night and E_night in any of these studies of Helianthus species (Fig. 1 ; Supplemental Table S1; P > 0.05 for all). The nutrient limitation was substantial enough to significantly reduce vegetative shoot biomass in all six studies (Table II ) and reproductive biomass in the studies where plant growth continued into the reproductive stage (Fall 2003-1 micro- and macronutrient manipulation, P < 0.05 for all species except H. deserticola; Fall 2004-1, Spring 2005, Summer 2005 nitrogen manipulation, P < 0.001; data not shown). Leaf total nitrogen content was also measured in four of the six nutrient manipulation studies. The limited nitrate treatment imposed as a modified Hoagland solution resulted in lower leaf nitrogen content (Table II). Leaf nitrogen was measured in only one study involving total macro- and micronutrient manipulation, and here the limited treatment resulted in significantly lower leaf nitrogen concentrations for H. annuus but not for H. anomalus or H. petiolaris.

View larger version (21K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 1. Effect of manipulating soil nutrient availability on gnight showing all of the tests for wild H. annuus. In Fall 2003-1, availability of all macro- and micronutrients was manipulated, whereas only nitrogen, available as nitrate, was manipulated in the additional four studies. Bars are lsmeans (least square means) ± 1 SE. See Supplemental Table S1 for nutrient treatment comparisons for H. annuus domesticate, H. annuus Hopi, and other Helianthus species.

Four studies applied soil water treatments (Table I): sufficient (maintained near field capacity) and limited. Plants with limited water showed substantially reduced g_night, E_night (P < 0.001), g_day, E_day, and photosynthesis (P < 0.05–0.001; Fig. 2 ; Supplemental Table S1). In the Fall 2004-2 study, g_night and E_night were assessed in both wild H. annuus and H. annuus Hopi, but there was no interaction between accession and response to soil water limitation for these traits (P > 0.05). During Fall 2005-2, xylem pressure potentials were measured at three points though the night and were consistently and substantially lower in the water-limited H. annuus (F_1,14 = 30.82, P < 0.001; Fig. 3 ).

View larger version (16K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 2. Effect of manipulating soil water availability on gnight during Fall 2003-2 (A), Fall 2004-2 (B), Summer 2005 (C), and Fall 2005-2 (D). In studies where both a water and nutrient treatment were applied (A and C), bars represent data from the high nutrient treatment only. Bars are lsmeans ± 1 SE. gcuticular for H. annuus and H. annuus domesticate, measured in Fall 2004-1, Spring 2005, and Spring 2006, ranged from 0.013 to 0.023 mol m–2 s–1.

View larger version (14K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 3. Variation in H. annuus gnight and Enight across a single night during Fall 2004-1 (A) and Fall 2005-2 (B) studies. Included are independent measurements of VPDa. Fall 2005-2 included measurements of xylem pressure potential (C) made on separate, randomly chosen plants from each treatment level. Points represent means ± 1 SE, n = 5 to 6 for gnight and Enight and n = 3 to 4 for xylem pressure potential. gcuticular for H. annuus, measured in Fall 2004-1, Spring 2005, and Spring 2006, ranged from 0.013 to 0.023 mol m–2 s–1.

A 24-h time course was measured for H. annuus in Fall 2005-2. g_day, E_day, and photosynthesis showed typical patterns, increasing rapidly in the morning and declining during the afternoon. g_night and E_night, though low compared to daytime rates, increased through the night in the sufficiently watered plants despite a small increase in atmospheric VPD (VPD_a) though the night (Fig. 3; time effect for g_night and E_night, respectively, F_2,11 = 31.2, P < 0.001; F_2,11 = 32.37, P < 0.001). In addition to instantaneous gas exchange measures, gravimetric measures were used to estimate total E_night and total E_day during the same time period. E_night of sufficiently watered plants was 0.86 (SE = 0.10) for instantaneous gas exchange and 0.22 (SE = 0.01) mmol m^–2 s^–1 for gravimetric measures. These rates were 5.7% and 6.5%, respectively, of the daytime rates measured by the same methods. Measures of E_night and E_day made with instantaneous and gravimetric methods were correlated (E_night r² = 0.78, P < 0.001, and E_day r² = 0.87, P < 0.001; Spearman rank correlations). During this same night and day period, average VPD_a in the greenhouse was 0.6 kPa (SE = 0.02) and 1.5 kPa (SE = 0.12), respectively.

Repeated measures of g_night and E_night were also made on sufficiently watered H. annuus in the Fall 2004-1 study and showed similar trends to those documented in 2005 (Fig. 3). g_night and E_night increased through the night (time effect, respectively: F_2,29 = 145.84, P < 0.001; F_2,29 = 358.69, P < 0.001) despite increasing VPD_a, and these trends were not affected by nitrate treatment (P > 0.5).

The effect of leaf aging on g_night and E_night was initially assessed in the Spring 2005 study. Repeated measures of g_night and E_night were made on the same leaves of H. annuus across 4 weeks, starting when leaves were recently fully expanded. Start dates for the 4-week measurement sets were staggered across several weeks and used in the analysis to account for random environmental variation between nights. There was no decline in g_night or E_night due to leaf aging (F_1,321 = 0.83, P > 0.3; F_1,321 = 0.57, P > 0.4, respectively; Supplemental Table S1). In the Fall 2005-1 study, leaf age effects were further assessed by comparing a young fully mature and older fully mature leaf of the same plant using sufficient nitrate treatment, 10-week-old plants. Here again, g_night and E_night did not differ with leaf age (t₁₄ = 1.21, P = 0.2; t₁₄ = 1.22, P = 0.2, respectively).

The effect of plant reproductive stage on g_night and E_night was assessed in the Fall 2005-1 study. For H. annuus, plant reproductive stage affected g_night and E_night under both sufficient and limited nitrate availability (F_2,46 = 17.45, P < 0.001; F_2,46 = 15.96, P < 0.001, respectively; Fig. 4 ; Supplemental Table S1). Prereproductive plants (5.5 weeks old) had higher g_night and E_night than did reproductive plants (10 or 15.5 weeks old).

View larger version (17K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 4. Effect of plant reproductive stage on gnight (A) and Enight (B) in H. annuus during the Fall 2005-1 study. Measurements were made on most recently fully mature leaves produced concurrently. Five and one-half-week-old plants were prereproductive, while 10- and 15.5-week-old plants were both reproductive. Bars are lsmeans ± 1 SE, n = 8 to 9.

During the Fall 2004-1 and Spring 2005 studies, g_cuticular, functionally defined as water loss though the cuticle with stomata at maximal closure, was measured on excised, wilted leaves. In Fall 2004-1, g_night (stomatal and cuticular conductances combined) was higher than g_cuticular for all four wild Helianthus species (Fig. 5 ). In Spring 2005, g_night was again higher than g_cuticular (Fig. 5). In both studies, g_cuticular measured on leaves was higher than instrument error (P < 0.001), which averaged –7.5 x 10^–6 mol m^–2 s^–1 during g_cuticular measurements. During Spring 2006, g_cuticular was measured on intact leaves of plants infused with exogenous ABA into the xylem. g_cuticular was lower than g_night measured on intact leaves of control plants for both wild H. annuus and domesticated H. annuus (Fig. 5).

View larger version (16K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 5. Instantaneous measures of gnight and gcuticular, functionally defined as conductance though both the cuticle and stomata at maximal closure. Measures of gcuticular were made on excised, wilted leaves during the Fall 2004-1 study (A) and Spring 2005 study (B) and on intact leaves of plants infused with exogenous ABA during the Spring 2006 study (C). Bars are means ± 1 SE, n = 5 to 6 bulked across nitrate treatment in Fall 2004-1, n = 9 bulked across nitrate treatment in Spring 2005, and n = 3 to 7 sufficient nitrate treated plants during Spring 2006. Measures were made on different leaves of the same plant in Fall 2004-1and Spring 2005 and made on separate control or ABA treatment plants during one night during Spring 2006. t values and associated degrees of freedom are presented from a paired t test in Fall 2004-1 and Spring 2005 and from an independent t test in Summer 2006 (*, P < 0.05; **, P < 0.01; ***, P < 0.001).

	DISCUSSION

TOP ABSTRACT RESULTS DISCUSSION MATERIALS AND METHODS LITERATURE CITED

 
The Helianthus g_night reported here for greenhouse-grown plants (0.023–0.225 mol m^–2 s^–1) are within the range reported for two of these species in their native habitats (Snyder et al., 2003; Ludwig et al., 2006) and for C₃ and C₄ plants in general (Caird et al., 2007). The wild and domesticated Helianthus species in our studies had typical values for g_day, E_day, and photosynthesis (Supplemental Table S1), and the g_night values were relatively large and greater than explained by g_cuticular.

In the Fall 2005-2 study, gravimetric measures were compared to instantaneous measures of transpiration. The gravimetric measures were approximately 4-fold lower, reflecting their integration over the entire night or day period, whereas instantaneous measures were timed to capture maximal E_night and E_day rates. However, there was a strong correlation between the two measurement techniques. Additionally, the percentage total E_night of total E_day measured gravimetrically over the 24 h gave an estimate of 6%, which agreed well with the 5% estimate from instantaneous gas exchange measures during the same day/night period. This added validity to our estimates based on instantaneous measures.

Response of g_night and E_night to Soil Nutrient and Water Manipulation

We hypothesized that regulation might occur for increased g_night under limited nutrient conditions to increase bulk flow of soil solution to the roots and reduce the development of a nutrient depletion zone in the rhizosphere. Although the soil nutrient limitations were sufficient to limit shoot and reproductive biomass and generally to reduce leaf nitrogen concentration, they did not affect g_night and E_night in any of the wild Helianthus species or in domesticated H. annuus. Thus, for Helianthus, there is no evidence of nighttime stomatal regulation in response to soil nutrient limitations. Contrary to our Helianthus results, we have evidence that other species do respond to soil nutrient limitations imposed while controlling for plant water status, some with higher g_night (Distichlis spicata, Populus balsamifera subsp. trichocarpa) and others with lower g_night (Arabidopsis [Arabidopsis thaliana]; M. Caird and A. Howard, unpublished data). A broader range of species needs to be tested to support any generalizations. The variable response of g_night to nutrient limitation may involve the same mechanisms that are currently being investigated for g_day responses, such as ABA, pH, and cytokinin signals (Dodd et al., 2003; Sakakibara et al., 2006).

Whether or not a species regulates g_night in response to soil nutrients, a plant that is transpiring at night may have increased uptake of nutrients such as nitrate. McDonald et al. (2002) demonstrated that Populus plants transpiring continuously (day and night), instead of only during the day, took up more nitrogen. Given that there is genetic variation for g_night and E_night (Arabidopsis; M. Caird, unpublished data), selection may favor high g_night and E_night in nutrient poor habitats if E_night provides a nutrient uptake benefit. The four wild Helianthus species studied here are native to habitats differing in nutrient availability; H. anomalus and H. deserticola are endemic to nutrient poor desert dune habitats (Rosenthal et al., 2002; Brouillette et al., 2007). We found that H. deserticola did have higher g_night and E_night than H. petiolaris, consistent with the direction predicted by selection for higher g_night in lower nutrient habitats, but the magnitude of difference was relatively small and appeared largely driven by greater g_cuticular in H. deserticola.

g_night and E_night did decline in response to water limitations that were generally sufficient to decrease leaf predawn xylem pressure potential, g_day, E_day, and photosynthesis. Declines were such that g_night in the limited water treatments was generally within the range we recorded for functionally defined g_cuticular. For three of the four studies, the water limitation was short term and consisted of withholding water just prior to measurements on fully mature leaves, so that the effect on g_night could not be due to a long-term change in leaf structure, stomatal density or size, or cuticle. The decline in g_night and E_night due to water limitation demonstrates that guard cell regulation of nighttime water loss is possible, analogous to daytime regulation of water loss in response to soil drying. Our results agree with previous results showing lower g_night associated with decreased plant water status in Hibiscus cannabinus (Muchow et al., 1980), Pseudostuga menziesii (Running, 1976; Blake and Ferrell, 1977), and H. anomalus (Ludwig et al., 2006), and a water stress treatment resulting in decreased water loss at night in wheat plants (Rawson and Clarke, 1988). The nighttime stomatal response to drought likely involves many of the same mechanisms that are currently being investigated for daytime responses, such as ABA and pH signals (Dodd, 2003; Davies et al., 2005; Li et al., 2006), although this remains to be determined.

Variation in g_night and E_night Nocturnally and across Leaf Lifespan and Plant Reproductive Stages

Assessing temporal variation is necessary for interpreting the significance of instantaneous leaf-level measures of g_night and E_night. We complemented single instantaneous measures on most recently fully expanded leaves of mature plants with studies that assessed variation nocturnally, across leaf lifespan, and across plant reproductive stages. Beginning with nocturnal variation (across a single night), repeated measures during the night in two studies both showed a significant increase in g_night and E_night. A similar gradual increase in g_night has been observed in several other species, including Arabidopsis, desert shrubs, and trees (Lasceve et al., 1997; Leymarie et al., 1998, 1999; Donovan et al., 2003; Bucci et al., 2004; Dodd et al., 2004, 2005), and potential regulatory mechanisms are being investigated (Lasceve et al., 1997; Gardner et al., 2006).

When g_night was measured across three nocturnal time points for sufficiently watered H. annuus in Fall 2005-2, the increase in g_night was associated with an increase in VPD_a, although of small magnitude (from approximately 0.5–0.7 kPa; Fig. 3). Thus, over this range of VPD_a, the correlation between g_night and VPD was not the negative relationship expected from daytime VPD_a responses (Franks and Farquhar, 1999). However, a larger range of VPD_a is needed to test nighttime VPD responses. Correlative data from other studies suggest that g_night does decline in response to increased VPD_a, similar to g_day, and responses may be species specific (Oren et al., 2001; Bucci et al., 2004; but see Barbour et al., 2005 for contrast). Bakker (1991) found a decline in g_night in response to experimentally manipulated VPD. However, more studies are needed that experimentally manipulate VPD_a and VPD_l and account for potentially confounding factors such as g_cuticular, circadian rhythms, and xylem pressure potential recovery.

We assessed variation in g_night and E_night across entire leaf lifetime. In contrast to Cechin and Fumis (2004), who found that g_day declined as Helianthus leaves aged, and Blom-Zandstra et al. (1995) who found that g_night declined as rose leaves aged, we found no decline in H. annuus g_night and E_night as recently matured (i.e. fully expanded) leaves aged over the following 4 weeks. Measures on the same plants indicated that leaf lifespan (number of days from 1-cm leaf blade length to 50% of leaf senesced) averaged 40 d (5.7 weeks). Thus, our gas exchange measurements captured the majority of leaf lifespan. The lack of decline in nighttime gas exchange rates over leaf lifespan suggests that for Helianthus, instantaneous g_night on a recently matured leaf may be used to scale up to instantaneous g_night for whole-plant leaf area, provided that there is an open canopy structure.

To generalize across plant life stages, we investigated variation in g_night and E_night across plant reproductive stages, controlling for leaf age. Prereproductive H. annuus showed significantly higher g_night and E_night than individuals that were flowering or setting seeds. Our results are consistent with those of Grulke et al. (2004) who found g_night to be higher in large saplings compared to mature ponderosa pine.

Young plants, during rapid vegetative growth, expend a large portion of respiratory energy on nutrient uptake, and this proportion generally declines as plants age (Marschner, 1995). Thus, although Helianthus species appear unable to regulate nighttime water loss in response to soil nutrient conditions, an inherently higher E_night for younger plants may be beneficial if it reduces formation of a nutrient depletion zone around roots at night, as suggested by results with the Barber-Cushman model (Barber and Cushman, 1981). Nutrient depletion zones may be more pronounced around roots of prereproductive plants due to a significantly lower root mass ratio (F_2,46 = 6.89, P < 0.01). Whether or not increased E_night represents a nutrient uptake benefit for prereproductive phase plants, it is possible that estimates of total water flux in mixed-aged stands or integrated over the life of a crop are underestimated when based on a combination of E_day and E_night measured only on reproductive-aged individuals.

The Contribution of g_cuticular to g_night

Measures of g_night and E_night include cuticular and stomatal pathways in parallel, yet only water loss through stomata, at an aperture greater than maximal possible closure, may be subject to guard cell regulation. For all wild Helianthus species except H. deserticola, g_stomata was 5 times greater than g_cuticular, suggesting that most nighttime water loss can be regulated. With the exception of the extremely high g_cuticular for H. deserticola, which deserves further investigation, the remaining g_cuticular for Helianthus were in the upper range of those reported in the literature using comparable techniques (Rawson and Clarke, 1988; Kerstiens, 1995; Boyer et al., 1997; Burghardt and Riederer, 2003; Nobel, 2005). More characterizations are needed of inter- and intraspecific variation in g_cuticular, including the extent to which growth conditions and atmospheric humidity can change g_cuticular components (Schreiber et al., 2001; Kerstiens, 2006; Kock et al., 2006).

Variation among Studies in Magnitude of g_night

Although our tests of g_night responses to nutrients and water occurred within each study, and cross study comparisons were not preplanned, the study differences in maximum g_night deserve some comments. For wild H. annuus in the nutrient and water manipulation studies, g_night of sufficiently watered plants ranged from 0.04 to 0.12 mol m^–2 s^–1 (Figs. 1 and 2; Supplemental Table S1). Because studies were conducted in different seasons and years, some of the variation may have been due to differences in the growth environment and to VPD_l differences during the nights and days of gas exchange measurements. However, the study with the lowest g_night (Fall 2005-1) did not stand out as having the highest VPD_l on the night or accompanying day of gas exchange measurements or an unusual VPD_a across the growth interval of the study. It is possible that using study means obscures a specific time interval where VPD_a affected leaf development and maximum g_night, but there are many other potential contributing factors. We recommend more exploration of growth environment (temperature, humidity, CO₂ levels, light quantity and quality, plant nutritional status, growth medium, etc.) on leaf structure, stomatal density and size, cuticular properties, and maximum g_night (Hetherington and Woodward, 2003; Bergmann et al., 2006; Kock et al., 2006). Additionally, the effects of VPD_a and VPD_l prior to and during the gas exchange measurements deserve more attention (Franks and Farquhar, 1999; Schreiber et al., 2001).

Across multiple studies, we demonstrate substantial g_night and E_night in Helianthus wild species and domesticates. For Helianthus, nighttime water loss occurs largely through stomata and is regulated in response to plant water stress but not soil nutrient availability. Additionally, Helianthus g_night varies nocturnally and across plant reproductive stages but does not vary for individual leaves as they age. More research is needed to test the commonality of these findings in plants of various life histories and native to diverse habitats. Building generalities for variation and regulation of g_night and E_night is necessary for predicting the conditions under which nighttime water loss will be biologically significant.

	MATERIALS AND METHODS

TOP ABSTRACT RESULTS DISCUSSION MATERIALS AND METHODS LITERATURE CITED

 
The objectives were addressed in nine greenhouse studies carried out at the Biological Sciences Plant Growth Facility at the University of Georgia, Athens (Table I). The studies included four wild annual Helianthus species (Helianthus annuus, Helianthus anomalus Blake, Helianthus deserticola Heiser, and Helianthus petiolaris Nutt.), commercial H. annuus cv Gray Stripe (referred to as H. annuus domesticate), and the Hopi domesticate of H. annuus (referred to as H. annuus Hopi). Achenes of the four wild Helianthus species were collected in Juab County, Utah, except for the H. annuus from Keith County, Nebraska used in the Fall 2003-2 and Fall 2004-2 studies, and the H. petiolaris collected in Washington County, Utah. The achenes of H. annuus domesticate used in Fall 2003-2 and Spring 2006 studies were obtained from Carolina Biological. The achenes of H. annuus Hopi (PI 432504 NPGS accession) used in the Fall 2004-2 study were originally collected from Shungopovi Village, Hopi Indian Reservation, Navajo County, Arizona.

The wild Helianthus species and the H. annuus Hopi achenes were germinated in petri dishes and transferred to pots after the seedlings developed root hairs. The H. annuus domesticate achenes were sown directly into the study pots. The study pots (20–25 cm diameter) contained a mix of sand and Turface (fritted clay, Profile Products), except for the Fall 2003-1 and Fall 2003-2 studies that used all sand. All plants were grown in a greenhouse with natural daylight supplemented to 12 to 14 h with metal-halide lamps. Temperatures were generally set to be at or above 26°C (day) and 16°C (night). For the six studies that had greenhouse weather available for the growth interval (Fall 2004-1, Fall 2004-b, Spring 2005, Summer 2005, Fall 2005-1, and Spring 2006), the average night VPD_a and day VPD_a across studies (n = 6) was 0.88 (SE = 0.11) and 1.57 (SE = 0.10) kPa, respectively.

Nutrient and Water Treatments

Nutrient treatments manipulated either total macro- and micronutrients (slow-release fertilizer, Osmocote Plus, Scotts-Sierra Horticultural Products) or manipulated just nitrogen (available only as nitrate). The latter was achieved with thrice weekly applications of a modified Hoagland solution containing 140 or 7 µg mL^–1 nitrogen as nitrate. The sufficient and limited nitrate Hoagland solutions contained equal amounts of potassium (176 µg mL^–1 K) and phosphorus (31 µg mL^–1 P). Additional macronutrients were calcium (50 µg mL^–1 in high; 10 µg mL^–1 in low), sulfur (8 µg mL^–1 in high; 120 µg mL^–1 in low), and magnesium (55 µg mL^–1 in high; 6 µg mL^–1 in low). Micronutrients included: Cl (0.443 µg mL^–1), B (0.068 µg mL^–1), Mn (0.027 µg mL^–1), Zn (0.033 µg mL^–1), Cu (0.008 µg mL^–1), Mo (0.012 µg mL^–1), and Fe (0.698 µg mL^–1 as FeEDTA). In the three studies without a nutrient treatment, the plants received either the high nitrate Hoagland solution or weekly application of 20:10:20 NPK soluble fertilizer (Peter's Peat-Lite Special, Scotts-Sierra Horticultural Products).

The soil water treatments consisted of supplying plants with ample water to maintain soils near field capacity (sufficient) and limiting the soil water availability (limited) either just prior to gas exchange measures or as a sustained treatment throughout the study. The limitation of soil water availability prior to gas exchange measures consisted of withholding water until visual wilting and depression of daytime gas exchange rates were achieved. The sustained water limitation in the Fall 2003-2 study consisted of watering every 4 to 5 d, beginning 2 weeks after germination. For the Fall 2005-2 study, leaf predawn xylem pressure potentials were sampled to accompany gas exchange measurements using a pressure chamber (Soil Moisture Equipment).

Gas Exchange Procedures

Leaf level measurements of daytime and nighttime gas exchange were made with a portable photosynthesis system (LI-6400, LI-COR). Measurements were made on a young fully expanded leaf of each plant, except when testing leaf age effects in the Spring 2005 study. The chamber light level was set to be 0 or 2,000 µmol m^–2 s^–1 during the night and day, respectively. To view equipment and plants at night, we used green safety headlamps with intensity not detectable by an LI-190 sensor (0 µmol m^–2 s^–1 photosynthetic photon flux density (LiCor) to avoid promoting stomatal opening. During the Fall 2004-1 study and part of the Spring 2005 study, leaves of some species were too small for the standard chamber, and an Arabidopsis (6400-15, LiCor) chamber was used. This chamber lacks an internal light source, and daytime measurements were therefore only taken on sunny days when photosynthetically active radiation exceeded 1,500 µmol m^–2 s^–1.

For both chambers, air temperature was set to ambient, and CO₂ was supplied at 400 µmol mol^–1. Flow was set to 125 to 200 µmol s^–1 at night and 700 µmol s^–1 during the day. Chamber fan speed was set to high. To partially compensate for removal of the boundary layer due to the chamber mixing fan, chamber relative humidity was manually manipulated to a target 5% to 10% above ambient (assessed with open chamber). The standard chamber directly measures leaf temperature, and before every set of measurements, the leaf thermocouple was checked to ensure it was reading accurately to within 0.1°C. Sample and reference infrared gas analyzers were matched prior to every plant for nighttime measurements. Measurements were also made with an empty chamber or with dry paper in the chamber every four to six leaf measures to assess instrument error. Averaged by study, estimates of instrument error obtained with the standard or Arabidopsis chamber at night yielded values for g from 0.001 to 0.016 mol m^–2 s^–1, which was always substantially lower than plant measures. Plant measures were logged when readings were stable and typically within 1 to 2 min of clamping onto the leaf.

Whenever possible, leaves were chosen that would fill the leaf chamber (6 cm² for standard chamber; 0.8 cm² for Arabidopsis chamber). When leaves that did not fill the chamber were used, all leaves in the measurement set (including those that filled the chamber) were marked before removal from the chamber to indicate placement of the chamber gaskets. The following day, gas exchange leaves were cut to remove all area that was not inside the chamber and scanned (Winfolia, Regent Instruments) to determine area. Leaves that did not fill the chamber were used in the Arabidopsis chamber in Fall 2004-1 (minimum area 0.45 cm²) and in the standard chamber in Fall 2005-1 (minimum area 4.5 cm²).

Daytime measurements were typically made between 9 AM and 2 PM, and nighttime measurements were typically made between 1 AM and the beginning of astronomical twilight (sun 12° below the horizon). Measures made at three times spaced though the night confirmed that this period captured maximum g_night but was well before a predawn stomatal opening would occur.

In the Fall 2005-2 study, nighttime water loss was measured both instantaneously using the LI-6400 as well as gravimetrically. Gravimetric measures of transpiration made over a 24-h time span were achieved by sealing the pot and root system in a bag, bagging all flower heads, and weighing at the beginning and end of the day and night periods. To obtain water loss per area, all leaves were harvested the following day, and total leaf area was measured using a LI-3100 leaf area meter (LiCor).

Assessment of Cuticular Water Loss

g_cuticular was defined functionally as conductance through the cuticle and stomata at maximum closure induced by either leaf wilting (water stress) or exogenous ABA application. As such, it includes both water loss through the cuticle and water loss through stomata at minimum aperture. The conductance provided by the LI-6400 (g_night or g_day in this study) is a total of both g_cuticular and g_stomata in parallel. Stomatal conductance at night was calculated as g_night minus g_cuticular (Nobel, 2005).

Cuticular water loss for excised, wilted leaves was estimated both by weighing (Rawson and Clarke, 1988) and by gas exchange measurements with the LI-6400. For weighing, excised leaves (cut end of petiole sealed with wax) were allowed to dry and wilt in the dark at ambient room temperature and VPD. Weights were taken approximately every 15 min, and, after initial rapid loss of water during which time stomata presumably closed, the linear relationship of water loss and time was used to estimate E_cuticular. During this period of linear water loss, g_cuticular and E_cuticular were also measured with the LI-6400 set to match ambient temperature and VPD. In the Fall 2004-1 study, E_cuticular from these methods, including all four species of wild Helianthus, were highly correlated (r² = 0.939, P < 0.0001, n = 24). Thus, only the instantaneous LI-6400 measurements of g_cuticular and E_cuticular are reported.

g_cuticular and E_cuticular were also measured on leaves for which stomatal closure had been induced by exogenous ABA application. ABA was fed into the xylem sap of sufficiently watered plants (Borel et al., 2001). Funnels were sealed around the stems of treatment plants and filled at predawn with degassed ABA solution [1.6 mol m^–3 synthetic (±) ABA, 0.4 mol m^–3 Ca(NO₃)₂, and 2.0 mol m^–3 KH₂PO₄]. Stems were drilled radially below the surface of the solution. Funnels were covered with silver foil and the solution was topped off as needed during the following day and night to ensure the drill hole was always below the surface of the solution. Plants were watered amply throughout the period of experimentation, and gas exchange measures were made on the first leaf above the infusion point.

Leaf Tissue Analysis

In most of the nutrient treatment studies, leaves used for gas exchange were collected after measurement, dried, ground, and analyzed for nitrogen content (Carbo Era NA 1500 CN analyzer). When a factorial design of water and nutrient treatments was present, only the plants in the high water treatment were analyzed for leaf nitrogen. In the Fall 2004-1 study, gas exchange measurements were made on two dates per plant, and these two leaves were combined for analysis of nitrogen content.

Biomass Measures

Plants were generally harvested after reaching reproductive maturity and when plants began to show shoot senescence. Plants in the Fall 2003-2, Fall 2005-2, and younger age classes in Fall 2005-1 studies were harvested before or shortly after the appearance of first flower. Plant shoots were divided into vegetative and reproductive components, dried at 60°C, and weighed.

Experimental Design and Statistical Analysis

Experiments were either complete randomized block designs or completely randomized (Table I). When gas exchange measurements were made across several days and nights, plants were grouped by block so that random effects due to night of measurement (e.g. VPD_a) were accounted for by the block effect. Measurements of different species or treatments made in one night and block were randomized to avoid confounding treatment results with effects of circadian rhythm or changing VPD though the night.

Most data were analyzed using a mixed-model ANOVA, with block treated as a random effect (PROC MIXED; SAS Institute, 2004, version 9.1) or with a general linear model ANOVA when blocking was not present (Fall 2005-2 study; PROC GLM; SAS Institute, 2004, version 9.1). In some cases, plant death, outliers, or difficulties with treatment application (e.g. ABA application, Spring 2006) resulted in an unbalanced design. When additional tests only involved two levels of a single variable, paired or independent t tests were used as appropriate. The Fall 2004-1 and Fall 2005-2 studies included repeated gas exchange measures during a 24-h period, and these data were analyzed in a repeated-measurement mixed model in PROC MIXED with an unstructured covariance matrix. In all analyses, variables were log transformed when necessary to approach model assumptions of normality of residuals and homogeneity of variance.

Supplemental Data

The following materials are available in the online version of this article.

Table S1. A summary of means and statistical results for results summarized in text for g_night, E_night, g_day, E_day, and photosynthesis.

	ACKNOWLEDGMENTS

 
The authors thank A. Tull, M. Boyd, M. Gebremedhin, F. Ludwig, M. Spharago, S. Howard, and B. Brouillette for assistance in the greenhouse, and J.H. Richards for comments on earlier drafts.

Received September 2, 2006; accepted November 22, 2006; published December 1, 2006.

	FOOTNOTES

 
¹ This work was supported by the National Science Foundation (grant nos. 0416627 to L.A.D. and 0416581 to J.H.R.).

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Ava R. Howard (ahoward{at}plantbio.uga.edu).

^[W] The online version of this article contains Web-only data.

^[OA] Open Access articles can be viewed online without a subscription.

www.plantphysiol.org/cgi/doi/10.1104/pp.106.089383

^* Corresponding author; e-mail ahoward{at}plantbio.uga.edu; fax 706–542–1805.

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