The effects of persistent drought and waterlogging on the dynamics of nonstructural carbohydrates of Robinia pseudoacacia L. seedlings in Northwest China
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The nonstructural carbohydrates (NSCs) of plants are posited to be crucial traits for the resistance and resilience of plants to climate change-induced drought and flooding. However, the potential effects of persistent drought and waterlogging on the dynamics of the NSCs and the underlying mechanisms are still poorly understood.
We measured the NSCs concentrations and pool size, photosynthetic rate and biomass of Robinia pseudoacacia L. seedlings for both 2015 and 2016 under five soil water treatments: 3%, 8%, 17%, 24% and 34% soil water content, representing extreme drought (ED), moderate drought (MD), the control group (CG), field capacity (FC) and waterlogging (WL) stresses, respectively. We observed the relationship between the pool size of NSCs and the survival of seedlings under water stress (drought and waterlogging) for 30 days in greenhouse.
Compared with CG, the net photosynthetic rate decreased 91%, 67%, 34% and 71%, and the biomass decreased by 37%, 15%, 16% and 33% under ED, MD, FC and WL, respectively. The total NSC (TNSC) concentration was significantly increased by 154% under ED after 10 days and sharply decreased by 50% under ED after 30 days. The concentrations of soluble sugars (SS) were significantly increased by 100% under MD after 10 days and sharply decreased by 60% under ED after 30 days. Compared with GC, the response of NSCs, photosynthetic rate and biomass under ED were more dramatic than that under WL. The pool sizes of fructose and sucrose were larger under ED and WL, but the maximum pool size of starch occurred under the CG. The depletion of NSCs was not observed under ED at the end of the experiments in both 2015 and 2016.
Our results indicate that the dynamics of NSCs is an important physiological feature of plant adaptation and resistance to drought and waterlogging. In addition, high sugars concentrations are beneficial for the plants during the short-term extreme drought and the longer term mild drought or waterlogging.
KeywordsCarbon pool Soil water Whole-tree Sugars Starch Tree mortality
The net photosynthetic rate
Analysis of variance
High soil water treatment (including field capacity and waterlogging)
The ratios of above- and below-ground
Reactive oxygen species
The ratio of soluble sugars and starch
Total nonstructural carbohydrates
Extreme event-induced tree mortality occurs globally and is likely to be exaggerated by future climate change, particularly drought and flood (Patz et al. 2005; Bréda et al. 2006; Huntington et al. 2006; Adams et al. 2009; Allen et al. 2010; Pachauri et al. 2014). As is well known, the events of extreme drought and floods will affect forest ecosystems along with rising temperatures, heat waves, and changing interactions between pests/pathogens and hosts (Bonan 2008; Allen et al. 2010). However, the underlying mechanisms of drought-induced tree mortality remain unclear (McDowell et al. 2008a, b; Sala 2009; Sala et al. 2010). In ideal condition over the time, tree mechanism is largely governed by the increasing stand level competition and social status on an individual tree (Saud et al. 2016, 2018), but under drought stress, trees are vulnerable to carbon starvation. Previous studies suggested that trees were vulnerable to carbon starvation under drought stress (Parker and Patton 1975; Bréda et al. 2006; McDowell et al. 2008a, b; Adams et al. 2009; Sala et al. 2010). However, there are the elusive and complex phenomena of nonstructural carbohydrates (NSCs) in plants in response to drought that are induced by different drought features (i.e., intensity and duration) and tree species, size, age and tissues (Sala et al. 2012; Hartmann et al. 2013; Palacio et al. 2014). Therefore, the lack of consensus among these studies on the effect of water availability on the NSC dynamics suggests that further studies are necessary to elucidate the underlying mechanisms (McDowell et al. 2008a, b; O’Grady et al. 2013).
Although studies on the effect of drought on NSCs is extensive, there has been few studies focusing on the effect of waterlogging (Board 2008; Parent et al. 2008; Nguyen et al. 2018). Sala et al. (2012) and Palacio et al. (2014) reported the manner in which we think about modeling tree growth and reviewed the literature on the minimum thresholds of nonstructural carbohydrates (NSC) under multiple environmental stresses. Some studies found that there was lack of direct evidence for the carbon-starvation hypothesis to explain water-induced mortality in plant (Sala 2009; Sala et al. 2010, 2012). Moreover, approximately 16% of land has been affected by waterlogging, resulting in severe economic losses (Luan et al. 2018). The assessment of the relationship between plant waterlogging and changes in NSCs concentration and allocation is very limited.
Some previous research suggested that different drought intensities induced different physiological responses of plants (Ditmarova et al. 2010; Osakabe et al. 2014) which may induce various NSC dynamics in trees to resist and survive under different water-stressed conditions (McDowell et al. 2008a, b). According to the previous hypothesis, mild drought stress may not result in the exhaustive depletion of NSCs, which may occur under severe drought stress, and trees may die from irreversible xylem cavitation (McDowell et al. 2011). However, there is a lack of research on the underlying mechanisms of NSC dynamics, particularly under drought (McDowell et al. 2008a, b) and waterlogging conditions.
In addition, not only drought intensity but also drought duration changes the NSC allocation and dynamics (McDowell et al. 2011). In the early stage of drought, the NSC concentrations may increase because the metabolic rate precedes the reduction in the photosynthetic rate (Korner 2003; Osakabe et al. 2014). However, as the drought stress persists, the reduction in the metabolic rate precedes that of the photosynthetic rate (Hsiao 1973; McDowell et al. 2011). Many previous studies focused only on the initial and final stage of the short-term drought manipulation (Regier et al. 2009, 2010; Anderegg and Anderegg 2013). Some previous studies also found that waterlogging as the dominant water stress within tree pits and thus avoidance of waterlogging conditions is required to stimulate increased tree growth (Grey et al. 2018; Ismail 2018). Therefore, it is necessary to understand how the duration of drought (McDowell and Sevanto 2010; Sala et al. 2010) and waterlogging (Sairam et al. 2008) changes the NSC dynamics in plants.
It has been demonstrated that different species have distinct functions and sizes of the NSC pool of different components (e.g., fructose, glucose, sucrose, starch, fructans and lipids) (Hoch et al. 2003; Würth et al. 2005; Millard et al. 2007; Palacio et al. 2014). Recently, there have been studies on the drought-induced allocations in carbon assimilation, transport, and utilization between the above- and below-ground tree tissues (Day et al. 2008; Klein et al. 2016). However, the accurate estimate of the NSC dynamics in whole trees is difficult and challenging for mature trees, because it has been measured only by C isotopes in a few studies (Ryan 2011; Dietze et al. 2014).
Therefore, it is necessary to study the response mechanisms of the NSC concentration of different tree species under drought and waterlogging stress with different intensities and durations. Robinia pseudoacacia (black locust) is a widely planted drought-resistant tree species in the Loess Plateau of China (Mantovani et al. 2014; Cao et al. 2018). It has unique features of rapid growth, drought resistance, resistance to barren soil and nitrogen fixation, and it can be used a model tree species to study the effect of water stress (drought and waterlogging) on tree growth and physiological acclimation. In this study, we manipulated different levels of the soil water content (ED: extreme drought, MD: mild drought, CG: control group, FC: field capacity and WL: waterlogging) and duration (10-day, 20-day and 30-day) to: 1) investigate the effect of drought intensity and duration on the NSC dynamics of R. pseudoacacia seedlings; and 2) examine the photosynthetic rate and plant growth to reveal the underlying mechanisms involved in NSC dynamics driven by drought and excessive water stresses. We hypothesized that 1) drought and waterlogging would significantly affect the NSC concentration, especially under ED condition; 2) a decrease in NSCs concentration would be observed at the later stage of the treatment, but not at the initial stage; and 3) plant NSCs respond more strongly to drought than to waterlogging.
We used a randomized block design with 4 replicates in 2015 and 2016, respectively. The NSC measurements were conducted on two-year old R. pseudoacacia L. seedlings grown in a greenhouse (located in the Northwest A&F University, Yangling, Shaanxi, China) for two consecutive years, 2015 and 2016. Seventy-two seedlings were used in both years. The seedlings were grown in 30-cm diameter and 40-cm deep pots. Each pot contained a mixture of nutrient-poor sand and local field soil (Cumulic Anthrosol) with a ratio of 1:5. The local soil was sieved (4-mm sieve) to remove roots, coarse organic matter and coarse sand prior to mixing. We fertilized all the pots with one-quarter strength Hoagland solution after transplantation to the pots. The seedlings were grown for four and a half months prior to the beginning of the water stress treatments to minimize biases due to the difference in the initial weight and/or height of the seedlings.
Effect of water status on gravimetric soil moisture across treatments, where Ext is extreme drought (no watering), MD and CG are at 30% and 70% of field capacity, FC is field capacity and WL is waterlogged
(2.46 ± 0.12)%
(7.23 ± 0.13)%
(16.481 ± 0.20)%
(24.02 ± 0.23)%
(33.31 ± 0.43)%
(2.70 ± 0.16)%
(7.89 ± 0.42)%
(16.85 ± 0.18)%
(24.65 ± 0.21)%
(33.96 ± 0.41)%
Nonstructural carbohydrate measurements
We measured NSCs with four randomly selected seedlings in both 2015 and 2016 prior to the start of the water treatments. NSC were measured at the end of the experiment on one randomly selected seedling from each water treatment from each block. The leaves, twigs, stems and roots were sampled separately for each seedling. The whole-seedling concentration and the pool of the TNSC is defined as the sum of the soluble sugars (including fructose, glucose and sucrose) and starch concentrations and pools, respectively.
Soil moisture and seedling biomass
The gravimetric soil water content was determined on a 20-g sample of sieved (2-mm mesh) and homogenized soil from each pot by oven drying at 105 °C for 24 h. We determined the biomass of the leaves, twigs, stems and roots separately for all seedlings. The materials were oven-dried for 48 h at 70 °C in kraft bags (12 cm × 15 cm) to a constant weight and then weighed.
A one-way analysis of variance (ANOVA) was used to examine the relationship between the SWC and dependent variables among the water treatments at the time of harvest. The data normality and homogeneity of variance were tested using the Shapiro-Wilk and Levene tests, respectively. We also tested the concentrations and pools of NSCs (soluble sugars, fructose, glucose, sucrose and starch) in each seedling for normality. In addition, we used a two-way ANOVA with a water treatment as a fixed factor and a block as a random factor to test the difference in SS and starch among the water treatments. The total seedling biomass as a covariate to account was included to scale the relationships between the plant size and response variables (Minucci et al. 2017). The familywise type I error rate for contrasts was controlled at ɑ = 0.05 using a Bonferroni correction. If there was no interaction, a post hoc separation of means was conducted using Tukey’s honestly significant difference (HSD) test. We also used a repeated-measures analysis of variance (ANOVA) to determine the effects of the soil water stresses (ED, MD, CG, FC and WL) and treatment durations (0-day, 10-day, 20-day and 30-day) on the net photosynthetic rates, dry biomass and the TNSC (soluble sugars = fructose + glucose + sucrose; starch) concentrations in each tissue. The assumption of sphericity was tested using Mauchly’s sphericity test (Mauchly 1940). The Bonferroni test was used to identify significant differences in the mean net photosynthetic rates, dry biomass, and NSCs concentrations in each tissue. The results were considered significant when P < 0.05. All statistical analyses were performed using SPSS v.20.0 (SPSS, Inc., Chicago, USA).
The effect of drought intensity, waterlogging and duration on the photosynthetic rate and biomass
The biomass under the drought stresses (i.e., ED and MD) decreased by 56% and 23% under ED and MD, respectively, compared to the initial value (0-day) (Fig. 2a and b). The biomass under ED decreased consistently over the course of experiment (P < 0.01) whereas it showed an opposite trend under CG. Under WL, the biomass first decreased and then increased with time.
The TNSC and SS concentrations in whole seedlings
The concentrations of NSC components (fructose, glucose, sucrose and starch)
The ratios of soluble sugars and starch in the seedlings
The ratios of above- and below-ground in NSC, SS and starch pools of seedlings
Effects of the treatment intensities on the total non-structural carbohydrates dynamics
We found that the NSC concentrations under extreme drought (ED) were significantly lower than those under the control group (CG) and high soil water conditions (FC and WL, included) at 20-day and 30-day. These results support our first hypothesis that drought stress would significantly influence the NSC concentration, particularly under ED at the initial stage of the treatments (10-day), which is consistent with recent findings (Zhang et al. 2015; Cao et al. 2018). However, their studies did not investigate different NSC components (fructose, glucose and sucrose) of soluble sugars. In contrast, waterlogging only had moderate legacy effects on the NSC concentrations and pools, and subsequently plant growth and productivity were not significantly affected. Even some historic studies showed that higher initial NSC pools were not advantageous for resistance and survival in plants (Pretzsch et al. 2018). But we observed that bigger NSC pool sizes play a key role under drought and waterlogging conditions during short-term.
Effects of the treatment intensities on the soluble sugars dynamics
It is important to note that soluble sugars play a crucial role in osmotic adjustment, vascular transport, and the repair of embolisms (Sala et al. 2012). The increase in soluble sugar concentrations has been reported in several previous studies (Latt et al. 2001; Silva et al. 2010). Increased concentrations of soluble sugars can remit the tree water potential, maintain cell turgor, and enhance water absorption by the roots from the soil (Handa et al. 1983; Silva et al. 2010; Williams et al. 2012). However, under drought conditions, our results were generally consistent with the previous findings that leaves can save carbon and directly make carbon available for plant growth (Kozlowski 1992; McDowell et al. 2008a, b; Dietze et al. 2014). In addition, the previous results suggested that plants used less and stored greater NSC, particularly conifer species (Michelot et al. 2012; Thomas and Martin 2012). However, a previous study found that broadleaf deciduous seedlings primarily contain more NSC in the roots than that at the whole-seedling level (Villar-Salvador et al. 1999, 2015). Other studies showed that there were no significant differences in the NSC concentrations between tree species (Hoch et al. 2003; Zhang et al. 2014). Our results are consistent with the generally accepted observation that higher NSC concentrations occurred under drought and high soil water conditions (FC and WL) compared to normal moisture conditions (Zhang et al. 2014, 2015; Cao et al. 2018). Our results were also consistent with those of the previous studies showing that the starch and soluble sugars have a transformational relationship under ambient pressure. This is mainly due to the reduction of temporarily stored starch in plants to compensate for the reduction of carbon assimilation and the maintenance of respiration and survival required for net photosynthesis from leaves. In particular, starch reaches a minimum during extreme environmental stresses (Chantuma et al. 2009; Li et al. 2013a, b). The reduction in biomass could be due to limitations in growth, structural carbon degradation and tissues (leaves and twigs) drop. In addition, the features of starch in plants facilitate its use as a long-term and accessible carbon storage, while soluble sugars act as an intermediate, ready-to-use energy and structure for growth and to resist stresses under biotic and abiotic conditions (Würth et al. 2005; Richardson et al. 2013; Bellasio et al. 2014; Richardson et al. 2015).
Effects of the treatment intensities on fructose, glucose and sucrose dynamics
Our results on the concentration of the SS components showed that there were similar patterns of variation in the TNSC and SS under drought stresses. However, the glucose concentration has the lowest value among the three components of SS. Maybe because glucose is involved in some biochemical synthetic processes and masked in the form of other compounds. Glucose has hormone-like functions and controls many vital processes through mostly unknown mechanisms in plants, may be more sensitive to stress signals (Cheng et al. 2002; León and Sheen 2003; Sheen 2014). The patterns of fructose and sucrose are consistent with recent studies (Li et al. 2011; Tauzin and Giardina 2014). In living plants, soluble sugars not only provide energy and carbon skeletons but also serve as signaling molecules to adapt to environmental stresses. Information on plant glucose and sucrose signaling is available, but to date, no fructose-specific signaling pathway has been reported (Li et al. 2011). In our study, fructose patterns were similar to those of sucrose. We could also conclude that fructose participated in signal and osmotic adjustments, although the results showed that the glucose variation trends were the most sensitive, especially under ED and MD.
Similarities and differences between drought and high soil moisture
In addition, drought stress led to an increased NSC concentration more significantly than those under field capacity (FC) and waterlogged (WL) across the experiments in both 2015 and 2016. Differences among the effects of soil moisture intensity on the NSC concentrations may result from the changes in the carbon source or sink and the underlying carbon allocation mechanisms. Some historical studies have found that under carbon source limited conditions (from photosynthesis), plants can increase their NSC storage and allocate it to survive at the expense of regular growth (Pantin et al. 2013; Wiley 2013; Saffell et al. 2014). In addition, Wiley (2013) found that trees can maintain higher NSC levels to survive with lower growth under moderate drought, while plants under severe drought (ED) had significantly lower NSC at the end of the experiments. In our study, net photosynthetic rates have been decreasing along with the drought and exceed-CG (FC and WL) stress gradients (Fig. 1a and b). As a result, the NSC concentrations under MD and WL were slightly higher than those under the CG, while NSCs under ED were significantly higher at the first sampling and lower than those under the CG at the second and third sampling (Fatichi et al. 2014). In addition, the synthesis of starch under ED and MD stress were inhibited to a greater extent than those under WL and FC, and the activity of hydrolases is sharply activated, leading to an increase in the ratio of soluble sugars to starch. Latt et al. (2001) reported the conversion of starch to sugars in all the tissues of the trees under drought stress. In our study, an increase in the concentration of soluble sugars and the ratios of soluble sugars to starch was also observed under all drought stresses (ED and MD). Silva et al. (2010) proposed that K+ and Na+ play crucial roles in osmotic adjustment under normal soil water conditions, while soluble sugars are more important under relatively stressful conditions, which may be due to the effects of hydraulic limitations that emerged earlier than carbon starvation (Adams et al. 2017). These results suggest that the R. pseudoacacia seedlings can adjust the osmotic potential through different pathways under drought and high soil moisture, because R. pseudoacacia could increase sugar concentrations to mitigate the increasing drought stress under ED and MD.
Under high soil water conditions (FC and WL), our results showed that the TNSC and SS were also increased, with slight fluctuations, but to a lesser degree than those under ED and MD. Waterlogging stops root growth and function because of the oxygen shortages that restrict root respiration. The concentrations of potentially toxic compounds increase in anoxic soils, which can enter through roots, damaging both root and above-ground tissues. Plants have some potential defense mechanisms to buffer waterlogging stresses through germinating aerial roots to survive. Hartmann et al. (2013, 2015) conducted experiments examining high soil water mechanisms and reported on those on conifers (Hartmann et al. 2013, 2015; Hartmann and Trumbore 2016). They found that carbon metabolism below-ground is related to the mechanism of tree mortality. Our results on fructose, glucose and sucrose showed that there were similar patterns of variation with the TNSC and SS, except for the lowest concentration of glucose. The whole process was observed, especially under drought conditions.
Effects of treatment duration on the NSCs dynamics
All the total non-structural carbohydrates (NSCs) concentration and dynamics of Robinia pseudoacacia L. seedlings under drought treatments were basically consistent but vary with different soil water treatments from the beginning to the final sampling. However, the NSC concentrations under ED decreased from 10-day to 30-day. In contrast, under MD, they significantly and stably increased over the course of the experiments in both 2015 and 2016. In addition, the net photosynthetic rate and biomass were significantly and synchronously decreased under ED, MD and WL but increased at 20-day under WL (see Figs. 2 and 3). Therefore, the carbon assimilation was reduced except for the middle and late period of WL in 2015 and 2016. These results support our second hypothesis that a decrease in NSCs would be observed when the drought period was longer but not during the initial drought phase. In addition, we observed that the concentrations of the TNSC, as well as the soluble sugars, were significantly greater at the 10-day than that at the 20-day and 30-day sampling times. However, previous research showed that there were similar results for red oak but the opposite results for white pine (coniferous species) (Richardson et al. 2015). Therefore, species type, plant tissues, sampling time and the protocol of the selection of sampling trees may be attributed to the discrepancy in these results (Dietze and Moorcroft 2011; Zhang et al. 2014). The NSC concentrations (TNSC, SS, fructose, glucose and sucrose) in most plants increased with decreased precipitation (Korner 2003; Würth et al. 2005), which is supported for our results and primarily due to the increased soluble sugars produced by starch degradation under drought conditions (Fig. 5). Waterlogging and the subsequent oxygen stress can lead to detrimental growth effects as it induces important physiological responses by plants and changes the nonstructural carbohydrates allocation in seedlings. Previous studies showed that stomata conductance and hydraulic conductivity are diminished under waterlogging (Vartapetian and Jackson 1997; Parent et al. 2008) and often a reduction in the rate of photosynthesis can be observed (Dreyer 1994; Pezeshki and DeLaune 1996). Metabolism in roots changes from aerobic (mitochondrial) respiration to anaerobic fermentation, leading to a depletion of carbohydrate reserves (Parent et al. 2008). However, the depletion of carbohydrate reserves was not observed in our studies, maybe due to the treatment durations were too short to be observed, and maybe mainly due to germinate some aerial roots at 20-day, so that once again unclogged the NSC pathways. As a consequence of these disturbances of vital physiological and metabolic processes, reductions of above-ground growth and main root growth are commonly observed in woody plants subjected to soil waterlogging condition (Frye and Grosse 1992; Kozlowski and Pallardy 2002; Glenz et al. 2006).
Effects of treatment intensity and duration on the NSCs dynamics
Previous studies have shown that the dynamics of NSCs in drought vary considerably among species and with the duration and intensity of the stress (Adams et al. 2009; McDowell et al. 2011). When converted into the ratio of soluble sugars to starch (RSS), the dynamics of the RSS differed significantly at four time sampling (P < 0.01, Fig. 5), due to variation among the replicates and microenvironments, and significant differences were noted among the treatments (Additional file 1: Figures S1 and S2). These phenomena can help to understanding of the interpretation of starch conversion into soluble sugars in plants to provide energy and regulate the osmotic potential to alleviate and resist drought and waterlogging over the short-term. Our results are partially consistent with the previous experiments in which herbaceous plants, short-lived with respect to woody plants, show constant or increased carbon storage during drought, very likely because of reduced translocation (Müller et al. 2001). The increase in the carbon storage pool and concentration also reflects the role of soluble sugars in osmoregulation and reactive oxygen species (ROS) regulation, both of which lead to basal alkalization, which destroys membrane function (Miller et al. 2008). However, photosynthesis was lower for longer duration than the initial stage, demonstrating that factors in addition to the negative carbon balance trigger plant carbohydrate metabolism (McDowell et al. 2008a, b; Adams et al. 2009, 2013; Sevanto et al. 2014).
Previous research has indicated that the timescale of various physiological processes during different drought stages plays an important role in understanding the NSC dynamics (Fatichi et al. 2014). In the short term, adaptation to the lag in photosynthesis may lead to the accumulation of starch and soluble sugars (Hsiao 1973; Korner 2003). In the medium term, the decline in photosynthesis before respiration can reduce the storage of NSCs due to their metabolism (Hsiao 1973; McDowell et al. 2011; Beier et al. 2012). In the long term, complex domestication mechanisms may be used to fine-tune tree growth via photosynthesis in order to ensure the storage of NSC (Kozlowski 1992; Hoch et al. 2003; Fatichi et al. 2014). However, the consumption of NSCs occurs under conditions in which trees cannot grow in harmony with photosynthesis (McDowell et al. 2008a, b). In our study, we observed higher NSC concentrations under both drought and waterlogging stress compared to those under the field capacity (FC), suggesting that the time frame of 30 d (from the initiation of soil water treatment to the third time sampling) was long enough for the downregulation of photosynthesis. The lower, but continuous, increase in the NSC concentrations under MD and ED from the beginning to the end might be the result of the acclimation mechanisms that allowed the seedlings to adjust the balance of carbon sink and source, preventing NSC depletion and sustaining survival and reserve accumulation under drought stress (Scartazza et al. 2013). The significant decrease in the NSC concentrations in the leaves, twigs and stems during the growing season under ED at the end of the experiment may result from the poor adjustment of growth, photosynthesis, and translocation of NSCs to metabolism. At the end of the two-year experiments, as the net photosynthetic rates under ED and MD significantly decreased, the seedlings under the CG maintained relatively sufficient NSC supplies by decreasing their soluble sugar storage and may increase starch reserves, while the seedlings under ED, whose growth have decreased or even stopped prior to this period, consumed NSCs to maintain normal metabolism.
Additionally, NSCs play fundamental roles in plant germination, growth, reproduction, and resistance and may also be conclusive to plant survival under negative stresses (Kozlowski 1992). In particular, NSCs are mobilized in trees to maintain respiration during stress, build biomass and sustain new growth in the future and supply energy for any adaptive responses to drought (Kozlowski 1992; Barbaroux et al. 2003). As is well known, R. pseudoacacia is an annular porous and Leguminosae species that needs to obtain new leaf reserves before germination to reach a large part of its annual stem growth (Bréda and Granier 1996; Landhäusser and Lieffers 2011). Annular porous species have a higher respiratory capacity than diffuse porous species (Barbaroux and Breda 2002; Barbaroux et al. 2003), and there are higher basal respiration rates and Q10 values in the plants (Edwards and Hanson 1996). Therefore, R pseudoacacia requires a larger amount of NSC under drought conditions than those under high moisture conditions, which is supported by our study in which the NSC concentrations decreased significantly under ED at the end of the two-year experiments. In addition, the RSS in the seedlings would continue to decrease from 0-day to 30-day but would still be higher than the initial value as well as the value of the control (CG) over time. If the starch is consumed in large quantities, it indicates that the plant needs soluble sugars to resist the stress. However, even under the ED conditions, the starch and soluble sugars were not exhausted at 30 days. Consequently, R. pseudoacacia seedlings under ED may be more vulnerable to high temperature and other biotic stresses during the experiments. Therefore, it would require additional study to explore the impact of high temperature on the variation of NSCs under drought and waterlogging conditions (Galvez et al. 2013). However, there are still several limitations in this study: 1) We studied the mechanisms of NSC dynamic changes under continuous drought and waterlogging conditions but did not clearly define the tipping point of NSCs for tree mortality, which used membrane failure and chlorophyll fluorescence to predict the plant mortality under drought (Guadagno et al. 2017); 2) We primarily studied the partitioning and dynamics of the TNSC, SS, starch, fructose, glucose and sucrose concentrations on the whole-tree scale. The change status did not use isotope techniques to accurately reveal the NSC allocation mechanisms; 3) we measured photosynthesis and biomass as covariates to clarify the NSC dynamic mechanisms without combining hydraulic characteristics. We should combine carbon starvation with hydraulic failure to explore the response of the trees to drought and waterlogging to understand possible mechanisms, and further research on this direction is urgently needed.
The main conclusions of this study are as follows: 1) the intensity and duration of soil water stress have significant effects on the NSC dynamics of Robinia pseudoacacia seedlings. 2) We observed a significant decrease in NSC concentration under severe drought stress, and the NSC concentration under MD and FC remained high levels. The NSC concentration under WL conditions recovered near the initial value. 3) Drought causes seedlings to preferentially increase NSC in below-ground tissues. While FC and WL can promote the distribution of NSCs mainly in the above-ground tissues. In summary, the dynamic characteristics (for strength and duration) and component types of NSCs in drought and waterlogged are important for elucidating the relationship between NSC dynamics and soil water stress. However, further research is needed to investigate the NSC dynamics during the dormant season, as well as the NSC allocation and storage characteristics of plant tissues under drought and waterlogging stress.
We greatly appreciate the help of Dr. Yi Zhang on the implementation of our experiments and seedling culture and water control in the greenhouse.
This study was mainly funded by the National Key R&D Program of China (2016YFC0500203), Qian Ren program and the Natural Sciences and Engineering Research Council of Canada (NSERC) Discovery Grant. The National Natural Science Foundation of China (41571081) and the National Key R&D Program of China (2016YFC0501804). The National Natural Science Foundation of China (41601098) and the Young Excellence Program for the Teachers of the College of Forestry, Northwest A&F University (Z111021603).
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Compliance with ethical standards
BY, CP and MW contributed conception and design of the study; BY organized the database; BY performed the statistical analysis; BY wrote the first draft of the manuscript; WL and MD revised the section of the manuscript. All authors contributed to manuscript revision, read and approved the submitted version.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
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