An external heat pulse method for measurement of sap flow through fruit pedicels, leaf petioles and other small-diameter stems

The external heat ratio method is described for measurement of low rates of sap flow in both directions through stems and other plant organs, including fruit pedicels, with diameters up to 5 mm and flows less than 2 g h⁻¹. Calibration was empirical, with heat pulse velocity ( v _h) compared to gravimetric measurements of sap flow. In the four stem types tested ( Actinidia sp. fruit pedicels, Schefflera arboricola petioles, Pittosporum crassifolium stems and Fagus sylvatica stems), v _h was linearly correlated with sap velocity ( v _s) up to a v _s of approximately 0.007 cm s⁻¹, equivalent to a flow of 1.8 g h⁻¹ through a 3-mm-diameter stem. Minimum detectable v _s was approximately 0.0001 cm s⁻¹, equivalent to 0.025 g h⁻¹ through a 3-mm-diameter stem. Sensitivity increased with bark removal. Girdling had no effect on short-term measurements of in vivo sap flow, suggesting that phloem flows were too low to be separated from xylem flows. Fluctuating ambient temperatures increased variability in outdoor sap flow measurements. However, a consistent diurnal time-course of fruit pedicel sap flow was obtained, with flows towards 75-day-old kiwifruit lagging behind evaporative demand and peaking at 0.3 g h⁻¹ in the late afternoon.     

Water relations in silver birch during springtime: How is sap pressurised?

• Positive sap pressures are produced in the xylem of birch trees in boreal conditions during the time between the thawing of the soil and bud break. During this period, xylem embolisms accumulated during wintertime are refilled with water. The mechanism for xylem sap pressurization and its environmental drivers are not well known.
• We measured xylem sap flow, xylem sap pressure, xylem sap osmotic concentration, xylem and whole stem diameter changes, and stem and root non‐structural carbohydrate concentrations, along with meteorological conditions at two sites in Finland during and after the sap pressurisation period.
• The diurnal dynamics of xylem sap pressure and sap flow during the sap pressurisation period varied, but were more often opposite to the diurnal pattern after bud burst, i.e. sap pressure increased and sap flow rate mostly decreased when temperature increased. Net conversion of soluble sugars to starch in the stem and roots occurred during the sap pressurisation period. Xylem sap osmotic pressure was small in comparison to total sap pressure, and it did not follow changes in environmental conditions or tree water relations.
• Based on these findings, we suggest that xylem sap pressurisation and embolism refilling occur gradually over a few weeks through water transfer from parenchyma cells to xylem vessels during daytime, and then the parenchyma are refilled mostly during nighttime by water uptake from soil. Possible drivers for water transfer from parenchyma cells to vessels are discussed. Also the functioning of thermal dissipation probes in conditions of changing stem water content is discussed.

     

红地球葡萄延后栽培成熟期水分运输研究

以3年生延后栽培的红地球葡萄为材料,在生育后期设置土壤水分处理控制在0.20(T_1)、0.25(T_2)和0.30 m~3·m~(-3)(T_3)左右,以果农常用的管理方法为对照(CK),在果实成熟期采用切片和田间树体茎流测定方法,研究果实水分运输结构变化和树体耗水状况。结果表明:(1)葡萄果实转色初期,果梗维管束的木质部结构完整且导管壁清晰可见;转色中期,果梗木质部部分导管壁变模糊,果刷中央维管束横切面积较转色前期变小;转色后期,果刷和果梗木质部导管壁模糊且破裂。(2)当葡萄果实可溶性固形物为7%时,果梗表皮细胞排列紧密且细胞间隙小,果刷维管束导管清晰可见;当可溶性固形物含量达到11%时,果刷中央维管束导管数量大于胚珠维管束,且分布不同;当可溶性固形物含量增加至15%时,果梗表皮细胞排列疏松,表皮细胞拉长,部分细胞发生破裂,果刷中央维管束和胚珠维管束的导管均出现解体。(3)9月11日左右,不同土壤水分处理(CK、T_1、T_2和T_3)茎液流达到最大值,峰值分别为3.51、3.95、4.37和4.59 d·L~(-1);葡萄转色中期,在低温影响下T_1的茎液流量整体显著低于T_2、T_3(P0.05),但与CK无显著差异;10月15日至10月26日无明显极端低温发生,不同处理树体茎液流量均呈下降趋势;11月下旬随着温度持续降低,树体各处理茎液流量迅速下降。研究发现,土壤含水量过高,低温发生时会造成树体茎液流量降低,增加土壤供水能够延缓葡萄可溶性固形物的积累,从而延缓葡萄成熟。     

Nutrient translocation in the xylem of poplar — diurnal variations and spatial distribution along the shoot axis

This investigation shows diurnal variations in the xylem sap composition of poplar (Populus tremula x P. alba). All major macronutrients reached a maximum concentration in the first half of the light period and decreased to the middle of the night. The relative abundance of the nutrients did not change during the day. The sap flow, which responded very fast to the environmental changes (2.2-fold increase within 10-20 min of illumination), reached a maximum value in the second half of the light period. Transpiration (and photosynthesis) was constant throughout the light phase. The calculated translocation rates displayed a maximum in the first half of the light period and therefore did not fit the time course of sap flow. During the night, translocation rates were 63-69% lower than the maximum. The regulation of nutrient translocation is discussed taking the active xylem loading into account. The axial distribution located the nitrate assimilation in younger leaves and storage of nitrate (and other macronutrients) in older leaves. Nitrate and potassium concentrations in the xylem sap did not change along the plant axis. However, the sap flow was greater in younger shoot sections than in older sections. We assume that the greater demand for nitrate in the younger shoot section was satisfied via an increased volume flow rather an increased nitrate concentration.     

Ion-mediated flow changes suppressed by minimal calcium presence in xylem sap in Chrysanthemum and Prunus laurocerasus

After the discovery of ion-mediated changes in xylem hydraulic resistance a few years ago, a number of research papers were published that related ion-mediated flow changes in the xylem to various aspects of whole plant functioning and evolutionary diversification of vascular cells. Ion-mediated changes in xylem hydraulic resistance are commonly quantified as the percentile change in hydraulic resistance, relative to the hydraulic resistance measured using a reference fluid, usually (ultra) pure deionized water. In this research the impact was investigated of the complete absence of all ions in deionized water compared with reference fluids containing a minimal amount of free calcium on the quantification of ion-mediated flow changes in stem segments of Chrysanthemum (Dendranthemaxgrandiflorum Tzvelev) and Prunus L. (Prunus laurocerasus L.). The addition of 10 mM KCl to deionized water significantly increased flow rate in Chrysanthemum (17-24%) and Prunus L. (16%). The addition of 1 mM CaCl(2) to the reference fluid reduced this KCl-mediated increase in flow rate to 1-2% in both species. 1 mM Ca(2+) is within the lower range of Ca(2+)-concentrations normally measured in xylem sap of many plant species, and three times lower than the original Ca(2+)-concentration measured in the xylem sap of Chrysanthemum plants used for the present measurements. The present results indicate that the complete removal of cations from the xylem fluid with deionized water causes the major part of the ion-mediated flow change previously reported in the xylem of plants. It is concluded that the use of deionized water as a reference fluid should be avoided. Earlier proposed relationships between ion-mediated changes and water flow in xylem of plants should be re-evaluated if they were based on deionized water as the reference fluid.     

Vascular Development and Sap Flow in Apple Pedicels

Xylem and phloem tissues of the pedicel of apple fruit increasein cross-sectional area throughout development. The increasein phloem is similar in the two cultivars examined (Cox's OrangePippin and Royal Gala) and reflects a steadily increasing phloemsap flow to the fruit. The increase in xylem tissue is due toa proliferation of non-conducting, structural, components sinceclose examination reveals no increase in the number of vesselelements from just after flowering onwards. The greater number,and the larger diameter, of the vessels in Cox's explains theinitially higher xylem conductance found in this cultivar. In vitro measurements of xylem exudation reveal a decline duringthe growing season in the xylem conductance of both cultivarsand an increasing proportion of fruit (particularly in Cox's)in which the xylem comes to be totally non-conducting. Thisobservation is in line with previously reported measurementsof xylem sap flow in vivo. The straightforward techniques used in this study offer a feasiblealternative to more arduous methods of assessing xylem and phloemsap flows and their balance during growth.Copyright 1994, 1999Academic Press Apple, xylem, phloem, vascular development, sap flow, Malus domestica Borkh     

Carbon balance in leaves of young poplar trees

In the present study, important components of carbon metabolism of mature leaves of young poplar trees (Populus x canescens) were determined. Carbohydrate concentrations in leaves and xylem sap were quantified at five different times during the day and compared with photosynthetic gas exchange measurements (net assimilation, transpiration and rates of isoprene emission). Continuously measured xylem sap flow rates, with a time resolution of 15 min, were used to calculate diurnal balances of carbon metabolism of whole mature poplar leaves on different days. Loss of photosynthetically fixed carbon by isoprene emission and dark respiration amounted to 1% and 20%. The most abundant soluble carbohydrates in leaves and xylem sap were glucose, fructose and sucrose, with amounts of approx. 2 to 12 mmol m(-2) leaf area in leaves and about 0.2 to 15 mM in xylem sap. Clear diurnal patterns of carbohydrate concentration in xylem sap and leaves, however, were not observed. Calculations of the carbon transport rates in the xylem to the leaves were based on carbohydrate concentrations in xylem sap and xylem sap flow rates. This carbon delivery amounted to about 3 micromol C m(-2) s(-1) during the day and approx. 1 micromol C m(-2) s(-1) at night. The data demonstrated that between 9 and 28 % of total carbon delivered to poplar leaves during 24 h resulted from xylem transport and, hence, provide a strong indication for a significant rate of carbon cycling within young trees.     

Dynamics of concentrations and nutrient fluxes in the xylem of Ricinus communis– diurnal course, impact of nutrient availability and nutrient uptake

Diurnal courses of nutrient transport in the xylem and their response to external availability of nutrients were studied. In soil culture, maximal concentrations in all analysed substances were observed during night‐time. Over experimental periods of up to 20 d, concentrations of some ions increased, most by accumulation in the soil. Stringent nutrient conditions were established in a novel pressure chamber. An aeroponic nutrient delivery system inside allows the sampling of xylem sap from intact plants under full control of the nutrient conditions at the root. Analysis of xylem transport under these highly defined conditions established that (1) diurnal variations in concentrations and fluxes in the xylem are dominated by plant‐internal processes; (2) concentrations of nutrients in the xylem sap are highly but specifically correlated with each other; (3) nitrate uptake and nitrate flux to the shoot are largely uncoupled; and (4) in continuous light, diurnal variations of xylem sap concentrations vanish. Step changes in nitrate concentrations of the nutrient solution established that (5) the concomitant increase in nitrate concentration and flux in the xylem is delayed by 2–3 h and is only transient. Diurnal variations of xylem sap composition and use of the new technique to elucidate xylem‐transport mechanisms are discussed.     

Effects of branch solid Fe sulphate implants on xylem sap composition in field-grown peach and pear: changes in Fe, organic anions and pH

The effects of placing solid implants containing Fe sulfate in branches of Fe-deficient pear and peach trees on the composition of the xylem sap have been studied. Iron sulfate implants are commercially used in northeastern Spain to control iron chlorosis in fruit trees. Implants increased Fe concentrations and decreased organic acid concentrations in the xylem sap, whereas xylem sap pH was only moderately changed. The citrate to Fe ratios decreased markedly after implants, therefore improving the possibility that Fe could be reduced by the leaf plasma membrane enzyme reductase, known to be inhibited by high citrate/Fe ratios. In peach, the effects of the implants could be observed many months post treatment. In pear, some effects were still observed one year after the implants had taken place. Results obtained indicate that solid Fe sulfate implants were capable of significantly changing the chemical composition of the xylem sap in fruit trees.     

Effects of drought on nutrient and ABA transport in Ricinus communis

We studied the effects of variations of water flux through the plant, of diurnal variation of water flux, and of variation of vapour pressure deficit at the leaf on compensation pressure in the Passioura-type pressure chamber, the composition of the xylem sap and leaf conductance in Ricinus communis. The diurnal pattern of compensation pressure showed stress relaxation during the night hours, while stress increased during the day, when water limitation increased. Thus compensation pressure was a good measure of the momentary water status of the root throughout the day and during drought. The bulk soil water content at which predawn compensation pressure and abscisic acid concentration in the xylem sap increased and leaf conductance decreased, was high when the water usage of the plant was high. For all xylem sap constituents analysed, variations in concentrations during the day were larger than changes in mean concentrations with drought. Mean concentrations of phosphate and the pH of the xylem sap declined with drought, while nitrate concentration remained constant. When the measurement leaf was exposed to a different VPD from the rest of the plant, leaf conductance declined by 400mmol m^?2 s^?1 when compensation pressure increased by 1 MPa in all treatments. The compensation pressure needed to keep the shoot turgid, leaf conductance and the abscisic acid concentration in the xylem were linearly related. This was also the case when the highly dynamic development of stress was taken into account.     

Modification of leaf apoplastic pH in relation to stomatal sensitivity to root-sourced abscisic acid signals

The confocal microscope was used to determine the pH of the leaf apoplast and the pH of microvolumes of xylem sap. We quantified variation in leaf apoplast and sap pH in relation to changes in edaphic and atmospheric conditions that impacted on stomatal sensitivity to a root-sourced abscisic acid signal. Several plant species showed significant changes in the pH of both xylem sap and the apoplast of the shoot in response to environmental perturbation. Xylem sap leaving the root was generally more acidic than sap in the midrib and the apoplast of the leaf. Increasing the transpiration rate of both intact plants and detached plant parts resulted in more acidic leaf apoplast pHs. Experiments with inhibitors suggested that protons are removed from xylem sap as it moves up the plant, thereby alkalinizing the sap. The more rapid the transpiration rate and the shorter the time that the sap resided in the xylem/apoplastic pathway, the smaller the impact of proton removal on sap pH. Sap pH of sunflower (Helianthus annuus) and Commelina communis did not change significantly as soil dried, while pH of tomato (Lycopersicon esculentum) sap increased as water availability in the soil declined. Increasing the availability of nitrate to roots also significantly alkalinized the xylem sap of tomato plants. This nitrogen treatment had the effect of enhancing the sensitivity of the stomatal response to soil drying. These responses were interpreted as an effect of nitrate addition on sap pH and closure of stomata via an abscisic acid-based mechanism.     

Effects of Osmotic Potential in Nutrient Solution on Diurnal Growth of Tomato Fruit

Tomato fruit on plants grown in circulating nutrient solutionexhibited a diurnal cycle in growth rate, measured as a changein diameter, with a maximum during thc day. The diurnal growthcycle was less evident in those fruit grown at high electricalconductivity (17 mS), or on days of reduced irradiance. Girdledfruit of low conductivity plants grew at a much reduced ratewith a diurnal cycle in reverse to that of ungirdled fruit,while girdled fruit of high conductivity plants showed no diurnalgrowth. The evidence suggests that phloem and xylem water transportinto fruit operate on opposite diurnal cycles. Partitioning of available xylem water in detached fruit betweenthe calyx and berry, as well as within the berry, was determinedby berry size and relative humidity in the air. Although berrytranspiration rate was unaffected by conductivity treatmentduring plant growth, water uptake capacity was greatly reducedin the berry from high conductivity plants, suggesting an increasedresistance in the xylem transport system within the fruit. Key words: Salinity, electrical conductivity, tomato fruit, xylem transport, transpiration     

MRI of long-distance water transport: a comparison of the phloem and xylem flow characteristics and dynamics in poplar, castor bean, tomato and tobacco

We used dedicated magnetic resonance imaging (MRI) equipment and methods to study phloem and xylem transport in large potted plants. Quantitative flow profiles were obtained on a per-pixel basis, giving parameter maps of velocity, flow-conducting area and volume flow (flux). The diurnal xylem and phloem flow dynamics in poplar, castor bean, tomato and tobacco were compared. In poplar, clear diurnal differences in phloem flow profile were found, but phloem flux remained constant. In tomato, only small diurnal differences in flow profile were observed. In castor bean and tobacco, phloem flow remained unchanged. In all plants, xylem flow profiles showed large diurnal variation. Decreases in xylem flux were accompanied by a decrease in velocity and flow-conducting area. The diurnal changes in flow-conducting area of phloem and xylem could not be explained by pressure-dependent elastic changes in conduit diameter. The phloem to xylem flux ratio reflects what fraction of xylem water is used for phloem transport (Münch's counterflow). This ratio was large at night for poplar (0.19), castor bean (0.37) and tobacco (0.55), but low in tomato (0.04). The differences in phloem flow velocity between the four species, as well as within a diurnal cycle, were remarkably small (0.25-0.40 mm s(-1)). We hypothesize that upper and lower bounds for phloem flow velocity may exist: when phloem flow velocity is too high, parietal organelles may be stripped away from sieve tube walls; when sap flow is too slow or is highly variable, phloem-borne signalling could become unpredictable.     

Chemical regulation of gas exchange and growth of plants in drying soil in the field

There is now substantial evidence that chemical regulation ofshoot physiology occurs in droughted plants in the field. Theevidence that ABA may play a role in such regulation is considered,and topics of relevance to the worker interested in determiningthe ABA relations of plants in the field; such as the methodsused for ABA quantification, the relevance of quantifying ABAin various plant tissues, methods of xylem sap collection andtiming of sap collection are reviewed. A possible role of tissuesensitivity to ABA in controlling the diurnal changes in stomatalconductance and leaf growth rate seen in the field is also considered. Key words: ABA, drought, stomatal conductance, leaf growth, hormonal sensitivity, xylem sap     

甘肃石羊河流域干旱荒漠区花棒蒸腾耗水量

研究了甘肃石羊河流域干旱荒漠区天然生长条件下花棒的蒸腾耗水规律．结果表明：花棒木质部液流速率随探针插入深度的加大呈“高-低”变化趋势;主根直径较小的花棒各位点的平均液流速率上升速度较快,变幅较大;不同主根直径花棒的液流量相差较大,但变化趋势较为一致,即昼夜变幅较大,夜间液流量较小,白天液流量较大,呈多峰曲线;日液流量与蒸发蒸腾量ET0呈线性相关,蒸腾耗水主要在6-9月,占生长季总蒸腾量的79．04％;花棒生长后期日液流量与0—50cm深沙层含水量呈显著相关,与其它层含水量无明显相关性;气象因素对花棒树干液流量影响的大小表现为日均气温〉空气水汽压差〉风速．     

不同灌溉量对塔克拉玛干沙漠腹地梭梭水分生理特性的影响

利用热平衡式茎流计和压力室,对不同灌溉量下塔克拉玛干沙漠腹地防护林植物梭梭的水分生理特性进行了测定.结果表明：梭梭茎干液流的日变化曲线随着灌溉量的不同而有所差异,灌溉量为每次每株35和24.5 kg条件下,茎干液流日变化曲线呈单峰型,且变幅较大,灌溉量为每次每株14 kg条件下,其日变化曲线为双峰型,变化较平缓;随着灌溉量的减少,梭梭日平均液流速率逐渐降低,其日单株耗水量也随之降低;随着灌溉量的减少,梭梭的清晨水势和午后水势逐渐降低, 且茎干液流速率与总辐射、空气温度、相对湿度和风速的相关性均增强,但不同灌溉量下,其与总辐射的相关性都最强.     

华北落叶松树体储水利用及其对土壤水分和潜在蒸散的响应: 基于模型模拟的分析

 树体储水在树木水分传输中具有重要的作用, 不仅为蒸腾提供水分来源, 还具有缓冲作用, 可防止木质部导管水势过低以至于水分传输的失败。树体储水动态及其利用的研究对于认识树木对水分胁迫的响应机制具有重要意义。该研究构建了包含树体储水释放-补充作用的树干水分传输模型, 可模拟计算林分小时尺度的冠层蒸腾、边材液流、树体储水与木质部导管水流交换过程, 并以六盘山北侧的华北落叶松(Larix principis-rupprechtii)人工林为例, 在林分水平分析树体储水利用及其 与土壤水分和潜在蒸散之间的关系。检验结果表明, 该模型能够精确地模拟出林分边材液流的日变化特征, 模拟与观测的小时液流速率决定系数R²为0.91 (n = 2 352)。模拟结果表明, 在典型晴朗天气下, 在日出时树体储水利用启动, 至9:00左右达到峰值(0.14 mm?h^–1), 午间降至0, 下午降为负值直至午夜, 即进入树体补水阶段; 树体储水日使用量(DJ_z)为0.04–0.58 mm?d^–1, 与日蒸腾量(DT_r)成正相关(R² = 0.91), 对蒸腾的贡献为25.6%。分析结果表明, 当潜在蒸散(ET_p)低于4.9 mm?d^–1时, ET_p是华北落叶松树体储水利用的主要驱动因子, DJ_z与ETp成正相关(R² = 0.68); 当ET_p高于4.9 mm?d^–1时, DJ_z随着ET_p的增加呈现降低趋势; DJ_z与土壤水势没有显著相关关系(p > 0.05), 但最大树体储水日使用量(DJ_zmax)与土壤水分含量成正相关(R² = 0.79), 说明土壤水分是树体储水利用的限制因子。     

Most Water in the Tomato Truss Is Imported through the Xylem,Not the Phloem: A Nuclear Magnetic Resonance Flow Imaging Study

In this study, we demonstrate nuclear magnetic resonance flow imaging of xylem and phloem transport toward a developing tomato (Solanum lycopersicum) truss. During an 8-week period of growth, we measured phloem and xylem fluxes in the truss stalk, aiming to distinguish the contributions of the two transport tissues and draw up a balance between influx and efflux. It is commonly estimated that about 90% of the water reaches the fruit by the phloem and the remaining 10% by the xylem. The xylem is thought to become dysfunctional at an early stage of fruit development. However, our results do not corroborate these findings. On the contrary, we found that xylem transport into the truss remained functional throughout the 8 weeks of growth. During that time, at least 75% of the net influx into the fruit occurred through the external xylem and about 25% via the perimedullary region, which contains both phloem and xylem. About one-half of the net influx was lost due to evaporation. Halfway through truss development, a xylem backflow appeared. As the truss matured, the percentage of xylem water that circulated into the truss and out again increased in comparison with the net uptake, but no net loss of water from the truss was observed. The circulation of xylem water continued even after the fruits and pedicels were removed. This indicates that neither of them was involved in generating or conducting the circulation of sap. Only when the main axis of the peduncle was cut back did the circulation stop.Fruits are terminal organs that depend completely on long-distance transport to supply them with sugars and water for growth. Water is imported by means of both the xylem and the phloem, whereas sugars are only imported by means of the phloem. Fruits have to compete for water with the rest of the plant, and for that reason, xylem influx is expected to be sensitive to changes in plant water potential. Xylem influx into fruits may thus be lower during the day and higher during the night. When in the apoplast the water potential is especially low, for instance, when the plant is transpiring a lot of water during a hot day, fruits may even experience a xylem efflux and lose water to the vegetative parts of the plant (Johnson et al., 1992; Guichard et al., 2005). It has been suggested that in several species, in order to reduce the sensitivity of fruits to changes in plant water status, during fruit development the xylem connection between fruit and plant is reduced or even severed (Findlay et al., 1987; Lang, 1990; Creasy et al., 1993; Lang and Ryan, 1994; van Ieperen et al., 2003; Drazeta et al., 2004). In contrast to the xylem, the phloem is expected to be relatively insensitive to diurnal changes in water potential (Ehret and Ho, 1986; Ho et al., 1987). For instance, in the main stem of a number of plants, the phloem was found not to respond to diurnal differences in plant water status, whereas the xylem did (Peuke et al., 2001; Windt et al., 2006).The tomato (Solanum lycopersicum) plant has been the subject of many studies dealing with long-distance transport to fruits and has been chosen as a model system in this study as well. It has been estimated that in tomato fruits, about 80% to 90% of the influx of sap takes place by means of the phloem (Ho et al., 1987; Plaut et al., 2004; Guichard et al., 2005). It has been proposed that the low xylem contribution is due to the presence of some form of restriction in the xylem connection between plant and fruit, possibly in the knuckle (Lee, 1989; van Ieperen et al., 2003). Despite the expected low xylem contribution and limited conductivity of the xylem connection between plant and fruit, fruits have been shown to exhibit a diurnal pattern of growth. In most cases, fruits have been observed to grow fastest at night (Lee, 1989; Grange, 1995; van de Sanden and Uittien, 1995; Guichard et al., 2005). The opposite has been found to occur as well (Ehret and Ho, 1986; Pearce et al., 1993), but in these cases, the faster daytime growth was probably caused by a low diurnal stress environment. In a number of studies, even an efflux of xylem sap and fruit shrinkage during the day was reported (Johnson et al., 1992; Leonardi et al., 1999, 2000). It has been proposed that, if the phloem and xylem operate under different diurnal cycles or if their relative contributions can be modified in any way by adjusting the environmental conditions in a greenhouse, it might become possible to control and regulate fruit yield as well as fruit quality and taste.Considering the importance of fruit for the world''s food production, surprisingly little is known about the dynamics of sap flow to fruits. Since the conception of the cohesion tension theory (Dixon and Joly, 1894) and the Munch pressure flow hypothesis (Münch, 1930), there has been a decent theoretical understanding of the basic forces that govern phloem and xylem flow. It has already been attempted to apply this understanding to model fruit growth for a variety of fruits and applications (e.g. Daudet et al., 2002). However, many of the parameters that are needed to model long-distance transport to fruits are currently outside of experimental reach. First, little is known about the pressure and water potential gradients that drive flow to fruits. The xylem and the phloem are extremely sensitive to invasive experimentation and are easily disturbed, and the water potentials in the fruits’ symplast and apoplast are difficult to assess. Second, it is not clear whether xylem and phloem sap only enters the fruit (unidirectional flow), or if return flow is possible as well, and if it is, under which conditions it may occur. As the results of this study show, NMR flow imaging can provide answers to these important questions.

Estimating Long-Distance Transport to Fruits

So far, the most important methods to estimate xylem and phloem influx in fruits have been the subtractive method (Lang and Thorpe, 1989) and the mineral accumulation method (Ho et al., 1987). In the subtractive method, the contribution of xylem and phloem are estimated by heat girdling the pedicel (fruit stalk) of a fruit. Heat girdling destroys the sieve tubes, stopping phloem influx, while the xylem is assumed to remain intact and functional. By comparing the growth of nongirdled fruits to that of girdled fruits, the phloem contribution can be estimated. The most critical assumption in this method is that the xylem sap flow is not affected by heat girdling. However, the validity of this assumption is not evident. First, because xylem and phloem flow to fruits are coupled. Xylem influx is driven by a water potential difference between the xylem and the fruit symplast, which is maintained by osmotically active compounds (sugars), which in turn are imported by means of the phloem. Fishman et al. (2001) showed that the coupling between phloem and xylem influx could give rise to significant errors when using the pedicel girdling technique. A second reason is that heat girdling may profoundly affect xylem function. The xylem tissue may apparently escape heat girdling unscathed, as demonstrated by Guichard et al. (2005), but if the surrounding cells are damaged, it is not unlikely that functional damage will occur. For instance, it has been proposed that the cells that surround the xylem protect it against embolisms by preventing the entry of air (Hacke and Sperry, 2001). Van Ieperen et al. (2003) found that in the tomato pedicel, the abscission zone is the site of highest xylem resistance and that only a few xylem conduits traverse it. If an obstruction would occur in these conduits, either by embolisms or by particles of debris, it could significantly affect xylem resistance and have large implications for xylem transport to the fruit.In the second method, the mineral composition of the fruit is used to estimate the relative xylem and phloem contribution. Ho et al. (1987) measured calcium accumulation, net water import, and fruit respiration in tomato fruits. The xylem contribution to fruit growth was then estimated based on a number of assumptions: (1) the calcium content of phloem sap can be neglected compared to that of xylem sap; (2) the calcium content of xylem sap is similar to that measured in root stump exudate; and (3) xylem backflow from fruits does not occur. However, in view of current knowledge, the first and third assumptions are questionable. Calcium is used in signal transduction and as such is known to be present in the phloem. The question is, in what concentration. In phloem sap exudate of castor bean (Ricinus communis) and eucalyptus (Eucalyptus globulus), calcium concentrations have been found that were about 66% and 25% of the concentration in the root stump exudate, respectively (Pate et al., 1998; Peuke et al., 2006). In Banksia prionotes, the calcium concentration in phloem exudate was even found to be 10 times higher than that of the xylem sap (Pate and Jeschke, 1995). It should be noted that in these studies phloem sap was harvested by cutting. This may have elicited a wounding response, causing elevated calcium levels in the phloem (Knoblauch et al., 2001). Still, we argue that these findings illustrate that the calcium concentration in the phloem cannot be assumed to be negligible, especially when the majority of influx of sap is thought to take place via the phloem. The assumption that backflow does not take place also may not hold. In a number of studies, backflow from tomato fruits has already been observed, especially under summer conditions or high vapor deficit (Johnson et al., 1992; Leonardi et al., 1999, 2000; Guichard et al., 2005). The subtractive and the mineral accumulation method thus are likely to be subject to large systematic errors. Better methods to estimate or measure long-distance transport to fruits are needed.

NMR Flow Imaging

Over the last 10 years, it has been demonstrated that NMR flow imaging can provide an excellent tool to measure xylem and phloem transport (Van As, 2007). NMR flow imaging does not only give information about the average flow velocity, such as heat pulse based methods do, but gives access to all properties of the flowing water, such as the flow conducting area, the distribution of flow velocities, and the volume flow, all on a per pixel basis (Scheenen et al., 2000b). So far, studies have been conducted measuring flow in the stem of a variety of plants, ranging from castor bean seedlings (Köckenberger et al., 1997) to fully developed tomato, castor bean, and tobacco (Nicotiana tabacum) plants, and a small poplar tree (Populus spp.; Windt et al., 2006). The technique has been used to study the diurnal variation in long-distance transport (Peuke et al., 2001; Windt et al., 2006), the effects of cold girdling (Peuke et al., 2006), and xylem embolism repair (Scheenen et al., 2007) and has been used as a reference technique to provide detailed velocity maps for comparison with different heat pulse methods (e.g. Helfter et al., 2007; D. Chavarro, C.W. Windt, M.W. Lubczynski, J. Roy, and H. Van As, unpublished data). These studies have in common that flow was only measured in the main stem of the plant. This is a convenient place to do flow imaging for a variety of reasons. In comparison with other flow-conducting structures in the plant, the stem is large, sturdy, and stable. It conducts the largest fluxes, and the xylem and phloem can be easily distinguished on the basis of their direction of flow. These properties make imaging xylem and phloem transport relatively easy.

Aims and Research Questions

In this study, we used NMR flow imaging to measure long-distance transport to fruits. As a model plant, tomato was chosen. The anatomy of the tomato truss, as well as the dimensions of the magnetic resonance imaging (MRI) device and its components, made it impossible to image the pedicel of a single fruit. The pedicels were too short and too close together to fit them with the radio frequency (RF) coil that is needed for MRI. For this reason, we chose to perform flow imaging on the peduncle of tomato, measuring the transport toward the entire developing truss. After fitting the plant in the imager, it was impossible to remove the plant without damaging it. The plant was therefore left in the imager and allowed to grow there for 8 weeks. In this period, we continuously monitored long-distance transport into the truss, aiming to answer the following questions: (1) can xylem and phloem flow into the truss be visualized and distinguished; (2) what transport tissues conduct sap into the truss during truss development; (3) is phloem and xylem transport into the truss unidirectional, or does backflow occur; and (4) can NMR flow imaging be used to draw up a quantitative balance of xylem and phloem influx into the truss?     

Diurnal changes in branch diameter as indicator of water status of Hinoki cypress Chamaecyparis obtusa

We investigated use of strain gauges for monitoring the water status of trees by measuring changes in the diameter of the largest spreading branch of a 27-year-old Chamaecyparis obtusa tree. The change in xylem diameter in the branch is more closely related than the change in phloem diameter to the change in leaf water potential. Since the diurnal changes in diameter match the diurnal changes in water balance (sap flow velocity - transpiration), measuring the change in xylem diameter using a strain gauge is useful in evaluating the water status of C. obtusa.     

Collection of Xylem Sap at Flow Rate Similar to in vivo Transpiration Flux

We have explored a method to collect xylem sap using a Scholanderpressure chamber for potted plants. Intact root system in potswhich fitted the pressure chamber was pressurised at a pneumaticpressure numerically equal to the absolute value of shoot waterpotential. The rate of xylem flow obtained from the stem stumpunder such pressure was found similar to the rate of transpirationbefore detopping. The rate of pressurised flow from detop-pedroots was linearly related to the pressure applied in both well-wateredand soil-dried plants. The osmotic concentration of the xylemsap was negatively related to the rate of volume flow, suggestingthe necessity to collect xylem sap at in vivo flow rate if originalsolute concentration is to be evaluated. The concentration ofABA in the xylem sap, however, did not show such a relationshipwith water flux. Both well-watered and soil-dried plants showedthe concentration of ABA in xylem sap largely stable with arange of volume flow rate, indicating a linear relationshipbetween the rate of ABA delivery through xylem and that of volumeflow. We also compared the concentrations of ABA in xylem sapsequentially collected from pressurised roots with that fromdetached shoots of the same plants. The concentration of ABAin the initial saps from shoots showed to be similar to thatfrom roots. However, a decrease in the concentration of ABAin the xylem sap collected from detached leaf or twig was observedwhen more volume of sap was collected, which might also be dependenton the plant species and the volume of xylem vessels concerned. (Received February 3, 1997; Accepted October 7, 1997)