Spatiotemporal dynamic changes in transpiration in the shoot sheath and its relation to water transportation during rapid growth of Moso bamboo

Introduction

Moso bamboo (Phyllostachys edulis), a native of China, is widely distributed in the tropical and subtropical areas of East and Southeast Asia and plays important roles in regional water and soil loss management, water restoration, and soil conservation (Song et al., 2017; Zhang et al., 2019). The species is known for the rapid growth of emerging shoots (Liese and Köhl, 2015), with growth rates reaching up to 10–80 cm per day (Liese and Köhl, 2015; Song et al., 2016). Furthermore, it takes only 1–2 months for this bamboo species to grow from shoot to culm through a stage known as the “explosive growth” stage (Song et al., 2016).

Water is an important solvent for plant cells as it affects various life activities and regulates plant growth rate. It is an important factor that not only directly affects plant growth and development but is also an essential component of physiological metabolism. In bamboo species, water supply is thus a determinant of shoot differentiation, the number of shoots available for harvesting, and the quality of new growth (Fu et al., 2005). Moso bamboo is connected by a subterranean rhizome system that serves as a conduit for water and nutrient exchange between different culms within the same clone (Wilsey, 2002; Xu et al., 2013). Studies have found that during the rapid growth phase of Moso bamboo, water is transferred from the stem through the root, and thus, the rapid growth of bamboo shoots is related to water transport from the mother culms to the shoots (Dierick et al., 2010; Zhang R. et al., 2017; Zhang Z. Z. et al., 2017).

Transpiration is commonly used to indicate the water status of plants as well as the interactions between plants and environmental factors (Ruiz-Pdrez et al., 2001). In this regard, the evaporative surface of the sheath is considered crucial in gramineous plants, particularly as the plant approaches a critical stage. Sheath transpiration significantly contributes to overall water loss in plants, particularly during the night (Sadok et al., 2020). When bamboo shoots and young culms are branchless and leafless, the shoot sheath serves as the primary transpiratory organ (Wang et al., 2018). The culm sheath is also directly connected to the outer vascular bundle, and its transpiration rate (T_r) and stomatal conductance (gs) are significantly higher than those of the leaf sheath (Wang et al., 2018). Moreover, the removal of the culm sheath affects the height of bamboo shoots (Shang et al., 2013; Wang et al., 2017). However, despite the multiple functions of the shoot sheath in the rapid growth phase of Moso bamboo, studies on the spatiotemporal dynamics of the T_r of the shoot sheath are limited.

Deuterium oxide (D₂O) tracing is an effective method for studying water transport among interconnected plants such as those connected by bamboo culms and rhizomes. In Bambusa blumeana, increased deuterium concentrations were detected in the leaves of culms of neighboring bamboos that had been treated with D₂O (Dierick et al., 2010). Thermal dissipation probes (Granier, 1985) in the clumps of Bambusa vulgaris also indicated water transport from mature culms to newly sprouted culms during the sprouting stage (Fang et al., 2019). Similarly, a 20% decrease in water use rates was noted after cutting rhizomes between neighboring culms (Zhao et al., 2017). Nevertheless, the relationship between water transport among culms of Moso bamboo and its effect on shoot sheath transpiration during the explosive growth stage has not been adequately explored.

In this study, we determined the spatiotemporal dynamics of T_r and gs in the shoot sheaths and analyzed the water distribution patterns in the shoots of Moso bamboo using the isotope tracer method. An acidic magenta aqueous solution was used to trace the water transport route. The objectives of this study were (1) to determine the spatiotemporal variations in shoot sheath transpiration and its effect on the rapid growth of bamboo shoots during the branchless, leafless stage and (2) to determine the water transport pattern and its relationship with shoot sheath transpiration. The findings of this study will provide a theoretical basis for water management during the explosive growth stage of Moso bamboo shoots.

Materials and methods

Measurement of environmental factors and plant height

The experiment was conducted in a Moso bamboo forest in Jing County, Anhui Province, China. We established three plots (10 × 10 m²), containing a total of 41 bamboo culms. Plant height was measured from the tip of the shoot to the culm using a CGQ-1 direct reading height gauge (Harbin Optical Instrument Factory Co., Ltd., China) between March 29 and April 28. Measurements were taken in the morning (06:00–08:00) and evening (18:00–20:00), ensuring a 12-h interval between successive measurements and two measurements every 24 h. Once the bamboo shoots attained a height of 4 m, three plants were randomly selected, and their heights were recorded every hour for 48 h.

The light intensity (Lx), air temperature (T, °C), and relative humidity (RH, %) were recorded every hour during the study period using Microclimate meters (Pocket Weather Tracker 4000, Kestrel Corp., USA), which were installed in the center of each plot. Thereafter, the vapor pressure deficit (VPD) was calculated using RH and T.

Determination of physiological indexes of shoot sheaths

T_r and gs were measured using a Li-COR 6400 photosynthesis apparatus (LI-COR, USA), with a light intensity of 800 mol/m²/s, CO₂ concentration of 400 μmol/mol, and temperature of 25°C. When the bamboo shoots attained a height of more than 4 m, a researcher needed to climb a ladder and record the measurements.

A total of 18 (out of 41) bamboo plants were selected from the three plots to measure the changes in T_r and gs in the shoot sheaths and culms of plants with an average height of 0.5, 1, 2, 4, 7, and 13 m (Figures 1b–d, f, g) and average diameter of 4–5 cm. The T_r and growth rate were measured for different bamboo plants. Nonetheless, the T_r and gs of three plants with similar heights were determined simultaneously from 08:00 to 10:00.

Figure 1

Figure 1. (a, e) Peeled-off sheath of 0.5-m bamboo shoot, the number (s1, s2, s3…s30) represents the location of the sheath in the bamboo shoots, the same as (c). The s-upper, s-middle, and s-lower parts of the culm sheath are marked, I represents the innermost layer of the culm sheath. (b–d, f, g) Photographs of 1-, 2-, 4-, 7-, and 13-m bamboo shoots. The number (s1, s2, s3…s15) represents the location of the sheath, the same as (a, e). S represents the top of the culm sheath; W stands for culm sheath of internode 13; T represents the upper part of the outermost-layer culm sheath; M represents the middle part of the outmost-layer culm sheath; B represents the bottom part of the outermost-layer culm sheath.

It was difficult to determine the T_r and gs in the interior of the sheath; hence, these parameters were measured for the exterior of the sheath, which was then peeled immediately to rapidly determine the values of these parameters in the interior of the sheath. In the process, bamboo shoots were damaged, and thus, another set of shoots was used for further estimations. Each sheath of the bamboo shoots was numbered (at different heights) as follows: 0.5 m (sheath number: 30, 21, and 23), 1 m (sheath number: 31, 31, and 23), 2 m (sheath number: 31, 31, and 31), 4 m (sheath number: 30, 31, and 31), 7 m (sheath number: 30, 21, and 23), and 13 m (sheath number: 37, 38, and 39). The peeled-off sheath is shown in Figures 1a, e. We measured the T_r and gs of the S-upper, S-middle, and S-lower parts of all the culm sheaths (s1 to sn; Figure 1a), and the area of each culm sheath was measured using the grid method (Zhuang, 1979). Then, average values of the T_r and gs of three bamboo shoots of similar height were analyzed.

As the unit of T_r was mmol/m²/s, the unit of transpiration water consumption (T_c) was converted to kilogram per meter square per hour to facilitate its estimation at different heights using the following formula: T_c = 0.0648T_r. The formula used to calculate the T_c of bamboo shoots over 8 h during the day (T_s, kg) is as follows.

$\begin{array}{l}{\text{T}}_{\text{s}}={\displaystyle \sum _{i=1}^n}{T}_{ci}{A}_{i}t(\text{n}=1,2,3,4\dots )\end{array}$

where T_ci is the transpiration rate of the sheath i (kg/m²/h), A_i is the area (m²) of the sheath i, t (8 h) is the time interval, and n is the number of culm sheaths.

Three bamboo shoots were then selected to measure the T_r and gs at 09:00, 12:00, 14:00, 15:00, 17:00, and 18:00. The values for the S-upper part of bamboo sheaths of s1–s5, s10–s15, and s15–s20 culms were measured without any damage to the plants. Thereafter, we calculated the average of the values obtained from different sheaths of a bamboo shoot and the values obtained for the same period.

Isotopic tracing in bamboo shoots

We found that the length of the internode of the shoots of heights 0.5, 1, 2, and 4 m was extremely reduced, and the amount of tissue fluid was low. Additionally, as lignification was severe in the internode of bamboo shoots with a height of over 7 m, the tissue fluid could not be extracted. Moreover, the T_r of 7-m-tall bamboo shoots was the highest; hence, they were selected for further estimations. Furthermore, the growth rate of bamboo shoots was not uniform. Therefore, three bamboo shoots with a height of 7 m (collected from 24 April 2019 to 30 April 2019) and another set of three shoots (collected between 30 April 2019 and 11 May 2019) were used for isotopic tracer experiments.

The mother bamboo of each shoot was identified using the rhizome. The surface soil of the sample plant was removed, and 10 mL of D₂O (99.9% D, Shanghai Research Institute of Chemical Industry, China) was injected into the base of the mother bamboo. Following Meinzer et al.'s (2006) method, fluid from shoot guttation was collected after injection. Figure 2 shows three white water-receiving devices (top, middle, and bottom) around each bamboo shoot. Fluid from guttation before sunrise was collected, and the T_r of the sheath was measured between 08:00 and 09:00 from the second day to the seventh day of the two experiments. The s1–s5, s10–s15, and s15–s20 culm sheaths (S-upper part) were selected to measure the T_r, and their average was determined. After 7 days, tissue fluid was collected from 5, 10, 15, 20, 25, 30, and 35 internodes of the shoots. All the samples were tested at the Shanghai Chemical Research Institute, and the relative isotope ratio (δD) in the guttation and tissue fluid was measured at the Shanghai Research Institute of Chemical Industry. During the study period, the annual temperatures were 25.6 ± 5.3°C and 25.5 ± 5.2°C, the average soil moisture was 28.02 and 29.5%, and the average RH was 93.58 and 88%.

Figure 2

Figure 2. Schematic drawing of isotopic tracing experiment; the green bamboo culm is the mother bamboo; next to the three bamboo shoots, the top, middle, and bottom, three parts of the bamboo shoots are equipped with the device of guttation reception.

The δD of guttation before injection was used as the baseline, and the isotope data were standardized according to the maximum value of δD. After standardization, the baseline value was 0, and the maximum value was 1. When the δD increased significantly (>10% from the baseline), it was recorded as time “h”. Simultaneously, the distance (D) between the bamboo shoot and the mother bamboo was measured to determine tracer velocity (m/h) as D/h.

Sectioning of bamboo shoots

Six bamboo shoots (height: 2 m) were treated with 1% (m/V) acidic magenta aqueous solution for tracing, according to the protocol reported by Xie et al. (2011). The bamboo shoots were randomly divided into two groups. The cavity at the bottom of the shoots in the first group was injected with a magenta solution at 06:00. After 24 h, the shoots were excised at the bottom to observe whether the magenta solution was transported upward along the bamboo cavity. The bamboo shoots in the other group were excised at the base and then immersed in the magenta solution for 24 h. Subsequently, the 10th internode was manually sliced to observe and record the transportation path of the dye. Each experiment was performed in triplicate.

Following Li et al. (2017), paraffin sections were cut from the middle part of the 10th internode at a height of 0.5, 1, 2, 4, 7, and 13 m. The middle part of each shoot was sliced (~1 × 0.5 cm²), fixed in formaldehyde: acetic acid: ethanol (5: 5: 90%) solution, and placed in a container equipped with a vacuum pump to extract air. Each section was dehydrated using a series of gradient alcohol solutions and embedded in paraffin. Then, 8-μm-thick transverse slices were stained with Tibetan Red for 10 min and Fast Green for 5–10 s. Thereafter, the slices were sealed with a neutral adhesive and observed under an Olympus BX51 microscope (Olympus Medical Systems Corp., Japan) equipped with a digital image acquisition system.

Statistical analyses

Data are presented as mean ± standard deviation. SPSS 26.0 was used for one-way analysis of variance (ANOVA), least significant difference test, and multiple comparisons (α = 0.05), and SPSS 26.0 and Excel 2016 were used to create the linear model and correlation graphs. We determined the coefficient of variation (CV) using the following formula: CV = standard deviation/mean. Pearson's correlation coefficients are presented in tables.

Results

Changes in the T_r and gs of the shoot sheath during the rapid growth phase

The average T, RH, VPD, and light intensity during the daytime were 21.21 ± 5.38°C, 64.56 ± 22.60%, 1.05 ± 0.91, and 3,455.25 ± 6,053.22 Lx, respectively. The average T, RH, and VPD values at night were 15.39 ± 4.22°C, 88.01 ± 12.03%, and 0.22 ± 0.28, respectively. Between 10 April 2019 and 12 April 2019, the lowest temperature was ~10°C, and RH at night increased by 40%. On 20 April 2019, the temperature peaked at 33°C, and on 13 April 2019, light intensity reached its maxima at noon (~39,349 Lx) (Figures 3A–D).

Figure 3

Figure 3. (A–D) Changes in light intensity, VPD, temperature (T), and relative humidity (RH) during the period of the rapid growth of bamboo shoots. (E) Height growth rate of bamboo shoots during the rapid growth period. (F, G) Height change of bamboo shoot and T_r and gs changes of shoot sheath during the rapid growth period. The curves represent the change in height of the bamboo shoots; the columns represent the T_r and gs of shoot sheath in 0.5, 1, 2, 4, 7, and 13 m.

The height of the 41 bamboo shoots was measured daily from 30 March 2019 to 27 April 2019. The bamboo shoots grew from 15.17 ± 11.19 cm to 1,310 ± 19.89 cm (Figures 3F, G). The growth rate of the bamboo shoots was low during the early stages when the average plant height was 1 m. Thereafter, the shoots grew more rapidly, reaching an average plant height of 2 m. After 19 April 2019, the growth rate of the bamboo shoots decreased, with an average plant height of 5 m. On 26 April 2019, the growth rate of the bamboo shoots, with an average plant height of 10 m, decreased significantly during the late stages (Figure 3E).

T_r and gs of the shoot sheath were the lowest when the shoot height was 1 m and the highest when the shoot height was 4 and 7 m, respectively (Figures 3F, G). The T_r of the lower parts (s1–s10) of bamboo culm sheaths was higher than that of the upper parts (s21–s31) when the shoot height was 0.5–7 m, but the trend was opposite in taller plants, with a height of 7 m (Figures 4A, B). However, the variations in T_r and gs in different parts of the shoot sheaths were not significant, although gs in the lower parts (Figure 1c) of the culm sheaths was significantly higher than those in other parts (Figures 4C, D). The T_s of bamboo shoots was the highest in plants of height 4 m (Figure 4E). Additionally, T_s was related to T and RH of the microclimate (P < 0.05) (Table 1).

Figure 4

Figure 4. (A, B) T_r and gs of shoot sheaths at different growth heights, lower was s1–s10, mid was s11–s20, and upper was s21–s31 bamboo sheaths. (C, D) T_r and gs of bamboo shoots in different sheath parts, blue and yellow represent day and night values, respectively. (E) Transpiration water consumption of shoots sheaths over 8 h a day of different heights; means with different letters are significantly different (LSD test, P < 0.05). 0.05). ^*indicates a significant difference (P < 0.05).

Table 1

Table 1. Correlation coefficient of microclimate change, transpiration, and plant height growth rate during the period of rapid growth of bamboo shoots.

Diurnal variations in the T_r and gs of the shoot sheath

From 11:00 on 18 April 2019 to 11:00 on 20 April 2019, the height of bamboo shoots, T, and RH were continuously monitored (Figures 5A, B). The height of bamboo shoots increased from 369.03 ± 13.69 cm to 469.3 ± 15.4 cm, and the growth rate was higher during the daytime and lower at night, with the highest growth rate occurring from 14:00 to 20:00 (Figure 5C). There was a diurnal variation in T_r and gs in 4-m-tall bamboo shoots; the values were significantly lower at noon and higher in the morning and evening (Figures 5D, E). The CV of the growth rate was significantly correlated with T_r (P < 0.05) (Figure 5F). However, there was no significant correlation between CV of the growth rate and gs (Figure 5G). Moreover, instantaneous Tr was significantly correlated with T, RH, and VPD (P < 0.01) (Table 1). The growth rate was influenced by light intensity (P < 0.01) and correlated with instantaneous T_r (P < 0.05) (Table 2).

Figure 5

Figure 5. (A, B) Diurnal variation of light intensity, T, RH, and VPD in 4-m bamboo shoots. (C) Diurnal variation of height growth rate of 4-m bamboo shoots. (D, E) Diurnal variation of T_r and gs of 4-m bamboo shoots, where L represents leaf sheath and S represents culm sheath. (F, G) Relationship between growth rate of plant height per hour and T_r and gs. Means with different letters are significantly different (LSD test, P < 0.05).

Table 2

Table 2. Correlation coefficient of diurnal microclimate, dural transpiration rate, and plant height growth rate in 4-m bamboo shoots.

Water transportation in bamboo shoots and its relationship with T_r

D₂O was injected into the mother bamboo connected to 7-m-tall bamboo shoots; guttation and shoot tissue fluids were collected; and the path of the isotope tracer was determined (Figure 6). The results showed that the δD of the two experiments was consistent. On days 3 and 7 after injection, the isotope was transported to the top of bamboo shoots from the mother bamboo through rhizomes, indicating that the injected isotope was not transported to the bamboo shoots by the mother bamboo at once. On day 12, δD was high in all internodes of the shoots, indicating that the isotope was completely transported from the mother bamboo (Figures 6A–D). The δD of guttation increased significantly with an increase in T_r (P > 0.05) (Figure 6E), whereas tracer velocity increased with an increase in T_r (P > 0.05) (Figure 6F).

Figure 6

Figure 6. (A) δD ratio changes in guttation of bamboo shoots in the first test. (B) δD ratio changes in guttation of bamboo shoots in the second test. (C) Trace results of δD ratio in tissue fluid of different stem heights at 3rd day and 7th day after D₂O injection in the first test. (D) Tracer results of δD ratio in tissue fluid of different stem heights at 7th and 11th days after D₂O injection in the second test. (E) Relationship between isotope δD ratio in guttation and T_r of shoot sheath. (F) Relationship between δD tracer velocity and T_r of shoot sheath; means with different letters are significantly different (LSD test, P < 0.05).

Water transportation path in bamboo shoots

A preliminary study was conducted on the water transportation pathway in bamboo shoots by soaking them in a fuchsine dye solution as well as injecting the fuchsine dye solution in situ (Figures 7A, E). The results revealed that the fuchsine dye solution was transported upward along the vascular bundles, and the staining was deeper in areas with larger conduits, near the medullary cavity (Figures 7B, C). A transportation pathway was thus observed along the transverse wall of the bamboo in the segments (Figure 7D). However, when the magenta solution was injected into the pulp cavity of the bamboo shoots, the dye was not transported upward through the pulp cavity (Figure 7A).

Figure 7

Figure 7. (A) Cross section of medullary cavity 24 h after injection to the bamboo cavity with a magenta solution. (B) Cross section of bamboo shoots after soaking for 24 h. (C, D) Longitudinal section of internode of bamboo shoots after soaking for 24 h. (E) Bamboo shoot is soaked in a magenta solution. Mc, medullary cavity; v, cross section of vascular bundle; lc, longitudinal conduit; ts, the transverse septum of the internode; c, culm of sheaths stripped off; s, sheaths.

Discussion

Relationship between shoot sheath transpiration, water transportation, and shoot growth

This study verified the relationship between the δD of bamboo shoot guttation and the T_r of shoot sheaths. In this study, the δD of guttation increased with an increase in T_r (Figure 6E). Previous studies have also shown that plants exhibiting high guttation show enhanced metabolism and rapid growth (Singh et al., 2013; Chen et al., 2019).

In this study, the T_r of the shoot sheaths varied with shoot height (Figure 4A). As the vascular bundle matured, it extended outward from the wall, thereby enhancing the water-carrying capacity and transpiration in the bamboo culm (Figure 8). Paraffin sectioning of bamboo shoots at various heights revealed the gradual development of vascular bundle cells as the shoots matured (Figure 8), which developed completely with duct sieves when bamboo shoots reached a height of 4 m (Figure 8D). Furthermore, the T_r values were higher when the shoot height was 4 and 7 m (Figure 3F).

Figure 8

Figure 8. (A) Structure of vascular bundle at 10th internode in 0.5-m bamboo shoots. (B) Structure of vascular bundle at 10th internode in 1-m bamboo shoots. (C) Structure of vascular bundle at 10th internode in 2-m bamboo shoots. (D) Structure of vascular bundle at 10th internode in 4-m bamboo shoots. (E) Structure of vascular bundle at 10th internode in 7-m bamboo shoots. (F) Structure of vascular bundle at 10th internode in 13-m bamboo shoots. pa, parenchyma; v, vessel element; ph, phloem.

The T_r of bamboo sheaths decreased at noon (Figure 5D) because of the variations in water vapor pressure that may have led to daily fluctuations in water use (O'brien et al., 2004; Kume et al., 2007) (Table 2). This was consistent with the findings of previous studies (Wang et al., 2018). However, the growth rate of bamboo shoots was the highest from 16:00 to 18:00 (Figure 5C), which was different from the findings of previous studies (Thapa et al., 2015; Fang et al., 2019) in which tropical bamboo was observed to grow rapidly at night. This could be attributed to the micrometeorological drivers that exhibited greater control over the bamboo forests in this study. The growth of bamboo shoots and daily height variations in Moso bamboo shoots correlated with instantaneous variations in T_r and light intensity (Figure 5F; Table 2). Previous studies found that the increase in liquid flow density was likely driven by enhanced solar radiation and ventilation, leading to increased transpirational demand in the canopies of the remaining culms (Whitehead et al., 1984; Teklehaimanot et al., 1991; Bréda et al., 1995; Sun et al., 2014).

In this study, the T_r of the lower culm sheaths (s1–s10) was higher than that of the upper culm sheaths (s21–s31) at shoot heights ranging from 0.5 to 4 m (Figure 4A). Previous studies have suggested that the rate of daytime photosynthesis in the upper part of the culm sheaths was consistently higher than that in the lower parts (Wang et al., 2018). Vertessy et al. (1995) suggested that T_r is influenced by the ecological structure of the plants and environmental factors. Additionally, the upper part of bamboo culm sheaths (s21–s31) was purplish-brown and densely covered with brown spines, whereas the lower part (s1–s10) contained scattered purple spots. Zheng et al. (2022) observed numerous vascular bundles in the lower part of culm sheaths, where a greater number of xylem ducts were apparent in a vascular bundle and their cross-sectional area exceeded that of the phloem. This suggested that lower parts of the culm sheaths (s1–s10) exhibit a high capacity for water transport. However, further studies are required to understand the relationship between T_r and these morphological characteristics.

Water transportation pathway in bamboo shoots during the rapid growth phase

Bamboo shoots and culms maintain water balance through an interconnected network of roots (Marshall, 1996; Hutchings and Wijesinghe, 1997; Wang et al., 2011; Zhang et al., 2012). In this study, the isotope tracer revealed that water was transported from the culm to the shoots through rhizomes during the explosive growth phase (Figures 6A–D), which was consistent with the findings of previous studies (Li et al., 1998; Song et al., 2016; Cao et al., 2018). However, the transported water did not reach all the shoots in equal quantities (Figures 6C, D). A likely explanation is that water was transported by diffusion from adjoining cells, and the amount of water transferred was associated with the leaf water potential or leaf area of the connected plants (Kroon et al., 1996; Adonsou et al., 2016). Nonetheless, this hypothesis requires further investigation.

Bamboo sheaths play a crucial role in shoot transpiration and respiration (Wang et al., 2018) as they regulate dynamic changes in water pressure and transport through guttation at night and transpiration during the day (Wang et al., 2020). We observed a significant increase in the δD of guttation with an increase in T_r (Figure 6E). This was attributed to the increased water transport velocities owing to transpiration (Figure 6F), which led to decreased water potentials and the generation of negative water pressures and potentials in the sink cells (Deng et al., 2020). According to the cohesion–tension theory, guttation is the process by which water is pumped out of parenchyma cells and phloem under tension (Fichtner and Schulze, 1990; Zhang et al., 2013; Savage et al., 2016). The shoots of Moso bamboo exhibited high transpiration rates, which could not be completely satisfied by the water absorbed through the rhizome system. Thus, mother bamboo supplemented the water supply through the rhizome system (Figures 6A–D), indicating that transpiration is a significant factor that influences water transport.

This study found that the pulp cavity of the bamboo shoots was unable to transport water (Figure 7A), and the vascular bundle adjacent to the pulp cavity of the bamboo wall served as the primary pathway for water transport (Figures 7B–D). Staining was also observed in the ducts of the bamboo nodal diaphragm (Figure 7D), Indicating that these interconnecting ducts played a crucial role in facilitating an efficient water-transport system in bamboo shoots (Zheng et al., 2022).

Conclusion

The instantaneous shoot height growth was associated with the Tr of the shoot sheath. The isotopic tracer experiment revealed that water transport from the mother bamboo to bamboo shoots occurred at a slow rate. However, water transport was a systematic and continuous process in Moso bamboo shoots. The continuous monitoring of transpiration and stem flow at different shoot heights were valuable contributions to this study. However, it was difficult to analyze water transportation in bamboo shoots without branches and leaves using traditional methods. Nonetheless, this study provides reliable data and a method to study water transportation in bamboo shoots.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Author contributions

JL: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. LC: Conceptualization, Writing – review & editing. JW: Investigation, Writing – review & editing. JX: Investigation, Writing – review & editing. HZ: Investigation, Writing – review & editing. YB: Investigation, Writing – review & editing. ZC: Investigation, Writing – review & editing. SM: Investigation, Writing – review & editing. JG: Conceptualization, Writing – review & editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported by the National Natural Science Foundation of China (Grant No. 32001379), the National Natural Science Foundation of China (Grant No. 31971737), and the Basic Scientific Research Fund Program of ICBR (Grant No. 1632021016).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

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