Ethylene Enhances Water Transport in Hypoxic Aspen

Abstract

Water transport was examined in solution culture grown seedlings of aspen (Populus tremuloides) after short-term exposures of roots to exogenous ethylene. Ethylene significantly increased stomatal conductance, root hydraulic conductivity (L_p), and root oxygen uptake in hypoxic seedlings. Aerated roots that were exposed to ethylene also showed enhanced L_p. An ethylene action inhibitor, silver thiosulphate, significantly reversed the enhancement of L_p by ethylene. A short-term exposure of excised roots to ethylene significantly enhanced the root water flow (Q_v), measured by pressurizing the roots at 0.3 MPa. The Q_v values in ethylene-treated roots declined significantly when 50 μm HgCl₂ was added to the root medium and this decline was reversed by the addition of 20 mm 2-mercaptoethanol. The results suggest that the response of Q_v to ethylene involves mercury-sensitive water channels and that root-absorbed ethylene enhanced water permeation through roots, resulting in an increase in root water transport and stomatal opening in hypoxic seedlings.

Hypoxia, a condition of oxygen deficiency in plant roots, is the main consequence of flooding or waterlogging. Plants respond to hypoxia with reduced root permeability, closure of stomata, hypertrophy of lenticels, epinasty, formation of aerenchyma, and adventitious roots (Vartapetian and Jackson, 1997). Ethylene accumulation is often assumed to be the factor responsible for many of the responses observed in plants exposed to hypoxia (Mattoo and Suttle, 1991; Abeles et al., 1992). Hypoxia induces the formation in roots of the immediate precursor of ethylene, 1-aminocyclopropane-1-carboxylic acid, which is transported in the xylem to the shoots and there rapidly oxidized to ethylene (Mattoo and Suttle, 1991). The synthesis of ethylene and the response of plants to ethylene differ among tissues and different plant species (Abeles et al., 1992), and can be affected by different internal and environmental factors (Sharp et al., 2000; Grichko and Glick, 2001).

The effects of ethylene on stomatal closure are not clear. Several studies on the effects of exogenous ethylene on stomatal movements demonstrated differential responses between the examined species (Taylor and Gunderson, 1986; Woodrow et al., 1988; Gunderson and Taylor, 1991; Abeles et al., 1992). Exogenous ethylene is known to increase membrane permeability in petal cells (Mayak et al., 1977; Borochov and Woodson, 1989); however, its impact on cell-to-cell water transport has not been thoroughly examined.

Water transport across intact higher plant cell membranes occurs predominantly through water channels (aquaporins; Chrispeels et al., 1997). Aquaporins are located in root cell membranes (Chrispeels and Maurel, 1994) at a high density (Johansson et al., 1998). In our previous work (Wan and Zwiazek, 1999, 2001; Kamaluddin and Zwiazek, 2001), we showed that the root water channels in aspen (Populus tremuloides) and Cornus stolonifera rapidly responded to changes in root metabolism. Phosphorylation of the aquaporins has been suggested to be the likely mechanism controlling water permeation through the cell membranes (Maurel, 1997; Johansson et al., 1998). There is evidence that plasma membrane aquaporin PM28A from spinach (Spinacia oleracea) leaves is a phosphoprotein and that its phosphorylation is carried out by a Ca²⁺-dependent membrane-bound protein kinase (Johansson et al., 1996).

Ethylene has been shown to induce very rapid and transient protein phosphorylation with the involvement of Ca²⁺-dependent specific protein kinases in the induction of pathogenesis related genes in tobacco (Nicotiana tabacum) leaves (Raz and Fluhr, 1993), epicotyl shortening in peas (Pisum sativum; Berry et al., 1996), and in the accumulation of 1-aminocyclopropane-1-carboxylic acid oxidase transcript in pea plants (Kwak and Lee, 1997). The ethylene-induced phosphorylation in pea tissues (Berry et al., 1996; Kwak and Lee, 1997) and in mung bean (Vigna radiata) hypocotyls (Kim et al., 1997) was inhibited with the application of a protein kinase inhibitor, okadaic acid. Okadaic acid also inhibited the phosphorylation of aquaporin phosphoprotein PM28A in spinach leaves (Johansson et al., 1996). These reports suggest that, through its effect on protein phosphorylation, ethylene may be involved in the regulation of water channel activities.

In the present study, we investigated the effects of exogenous ethylene on root water transport in aspen seedlings. We studied the hypothesis that the exposure of roots to ethylene would increase the transport of water in physiologically depressed roots of hypoxic seedlings. We measured the root hydraulic conductivity (L_p), stomatal conductance (g_s), and root respiration in hypoxic seedlings before and after exposing the roots to ethylene. To confirm the effect of ethylene, we used an ethylene action inhibitor, silver thiosulphate (STS), and determined its effect on L_p in ethylene-treated plants. To determine the extent to which mercury-sensitive water channels are involved in ethylene-induced water transport, we also examined the effect of mercuric chloride on pressure-induced root water flow (Q_v) in ethylene-treated roots.

RESULTS

Morphology of Hypoxic and Aerated Seedlings

A decline in growth rates of hypoxic seedlings was noticeable and drooping of leaves and hypertrophy of lenticels were evident. Aerated seedlings did not show leaf drooping; however, some hypertrophy of lenticels was also observed.

Response of g_s to Hypoxia and Exogenous Ethylene

Root hypoxia resulted in a decrease in g_s over time (Fig. 1A). A significant decrease in g_s was observed within 1 d of hypoxic treatment. The decline in g_s continued to d 11 when it measured less than 25% of the rates recorded for control seedlings. The g_s values of aerated seedlings remained at a similar level throughout the experimental period.

Figure 1.

Effects of hypoxia and ethylene applied to roots of hypoxic plants on g_s (A), L_p (B), and root respiration (C). Each data point represents mean (n = 5) ± se. Ethylene was applied to hypoxic seedlings at 9 pm on d 10 and measurements were taken on d 11.

The hypoxic roots exposed to ethylene for 12 h, including an 8-h-dark period, showed over a 2-fold increase in g_s (Fig. 1A). The g_s values of hypoxic seedlings treated with ethylene remained significantly higher than those of hypoxic seedlings throughout the measurement period, although there was a gradual decline in g_s, over time on d 11 in ethylene-treated hypoxic seedlings as well as in well-aerated seedlings. There was no significant change in g_s in untreated hypoxic seedlings over time on d 11.

L_p in Response to Hypoxia and Ethylene

L_p significantly decreased in response to hypoxia (Fig. 1B). Similarly to g_s, a significant decrease in L_p was found within 1 d of hypoxic treatment and further decline continued until d 5 (Fig. 1B). L_p of well-aerated seedlings remained little changed throughout the experimental period.

Ethylene applied to the hypoxic seedlings at the end of d 10 triggered a drastic increase in L_p. When measured 12 h after ethylene treatment, there was a 3-fold increase in L_p of hypoxic plants (Fig. 1B). Unlike g_s, L_p did not change appreciably over the measurement period on d 11 in ethylene-treated hypoxic, untreated hypoxic, and aerated control seedlings.

Root Respiration in Response to Hypoxia and Ethylene

Root respiration significantly decreased as a result of hypoxia (Fig. 1C). After 3 d of hypoxic treatment, root respiration rates declined to about 50% of those measured in aerated seedlings (Fig. 1C).

Ethylene significantly enhanced root respiration in hypoxic seedlings (Fig. 1C). Within 12 h after the application of ethylene, respiration rates of hypoxic plants were at over 80% level of the respiration rates measured in well-aerated control roots (Fig. 1C). Both ethylene-treated hypoxic and untreated hypoxic seedlings showed some decline in respiration rates over time on d 11 (Fig. 1C).

L_P in Ethylene-Treated Plants Exposed to STS

Applied ethylene significantly increased L_P in aerated seedlings (Fig. 2). Ethylene-treated aerated roots showed a 25% increase in L_P compared with the values measured before ethylene treatment (P < 0.037). This increase in L_P was observed within 15 min of pressurization. STS significantly reversed the enhancement of L_P by ethylene (P < 0.044) when measured after 4 h of STS treatment. STS had no effect on L_P of roots that had not been treated with ethylene (P < 0.524).

Figure 2.

Effects of STS on ethylene-enhanced L_p of aspen seedlings. Each data point represents mean (n = 7) ± se. The black bars indicate the control group and the white bars indicate the ethylene-treated group. The same root system of each group was measured after application of ethylene and/or STS.

Mercurial Inhibition of Q_v in Ethylene-Treated Roots

Pressure-induced Q_v in ethylene-treated root systems increased by about 50% compared with the flow rate before treatment (Fig. 3). Q_v in the untreated root systems remained constant throughout the measurement period (Fig. 3). Root systems treated with 50 μm HgCl₂ showed a gradual decline in Q_v. The decline commenced within 10 min after the addition of 50 μm HgCl₂ and within 1.5 h, Q_v decreased to about 65% of the pretreatment flow rates. A similar magnitude of decline in Q_v was observed in ethylene-treated roots when HgCl₂ was added to the bathing solution. In ethylene-treated roots, Q_v decreased to about 66% of the ethylene-treated flow rate after adding 50 μm HgCl₂ (Fig. 3). The inhibition in Q_v by HgCl₂ was partly reversed by the addition of 20 mm ME to the bathing solution. After the addition of ME, Q_v increased to 80% of the pretreated flow rates in root systems not treated with ethylene within 30 min, and at the same time the recovery in ethylene-treated roots was 87% with the addition of ME.

Figure 3.

Effects of exogenous ethylene and mercuric chloride on Q_v of aspen seedlings. Each data point indicates mean (n = 6) ± se. Arrows indicate the time of treatment with ethylene, mercuric chloride, 2-mercaptoethanol (ME), or water (control).

DISCUSSION

Root hypoxia brought about a substantial decrease in g_s with a concomitant decline in L_p and root respiration in aspen seedlings (Fig. 1). Our data suggest that the reduction in L_p by hypoxia was likely because of the inhibition of water transport through the aquaporins. The presence of water channel proteins in the plasma membrane and the tonoplast allows a plant to regulate its water flow through the cell-to-cell pathway (Chrispeels et al., 1997). Metabolic dependence of Q_v and the effects of respiration on water channel function have been reported for different plants (Tyerman et al., 1999; Wan and Zwiazek, 1999; Zhang and Tyerman, 1999; Kamaluddin and Zwiazek, 2001; Wan et al., 2001). In wheat (Triticum aestivum) root cells, the extent of inhibition of cell hydraulic conductivity was similar in roots treated with HgCl₂ and hypoxia and interpreted as a result of the decreased phosphorylation of aquaporins (Zhang and Tyerman, 1999). NaN₃, a potent inhibitor of oxidative phosphorylation, is also known to rapidly inhibit Q_v across membranes (Kamaluddin and Zwiazek, 2001). Water transport through some aquaporins is regulated by phosphorylation (Daniels et al., 1994; Maurel et al., 1995; Johansson et al., 1998). Stress-induced reduction in L_p can be caused by the decreased phosphorylation of aquaporins (Johansson et al., 1996, 1998). Therefore, it is conceivable that reduced phosphorylation of root cell aquaporins might be the cause of the decreased L_p that we observed in hypoxic seedlings.

In our study, ethylene applied to hypoxic seedlings enhanced g_s with a concomitant increase in L_p and root respiration (Fig. 1). Although we did not examine the effects of ethylene on the phosphorylation-dephosphorylation of water channel proteins in this study, it is plausible that these events could be involved in this response. Under the condition of oxygen deprivation, the amount of ATP produced in the plant roots decreases (Reid et al., 1985). The decrease in L_p might be partly because of the inhibitory effects of hypoxia mediated through the decreased root respiration rates. There was a simultaneous decline in g_s as a result of hypoxia (Fig. 1A). In a previous study (Wan and Zwiazek, 1999), we demonstrated that mercury-sensitive processes in roots were responsible for triggering stomatal closure in aspen leaves. It is plausible that similar processes were responsible for stomatal closure in hypoxic plants.

The role of abscisic acid (ABA) in the observed responses of plants to ethylene cannot be discounted. Ethylene has been reported to trigger ABA synthesis (Abeles et al., 1992; Hansen and Grossmann, 2000) and ABA triggers stomatal closure in stressed plants (Zeevaart and Creelman, 1988). Both ABA and gibberellic acid are also known to activate the promoter of the aquaporin PIP1b (Kaldenhoff et al., 1993, 1996) and some studies reported an increase in L_p of ABA-treated roots (Ludewig et al., 1988; Freundl et al., 1998; Hose et al., 2000), possibly by its effect on aquaporins (Abe et al., 1997; Hose et al., 2000). On the other hand, Wan and Zwiazek (2001) demonstrated that ABA applied to roots of hydroponically grown aspen seedlings reduced g_s but not root L_p and other studies showed that ABA biosynthesis and transport to shoots is restricted under the oxygen shortage conditions (Zeevaart et al., 1989; Else et al., 1995). Therefore, ABA may not be the primary factor triggering changes in stomatal opening and L_p of hypoxic plants.

The effect of ethylene on phosphorylation of aquaporin proteins is yet to be investigated. There is, however, evidence that ethylene induces a rapid and transient protein phosphorylation in tobacco leaves, and a protein kinase inhibitor, H-7,1-(5-isoquinolinylsulfonyl)-2-methylpiperazine, blocked ethylene-induced pathogenesis-related protein accumulation (Raz and Fluhr, 1993). A rapid change in the pattern of protein phosphorylation was also induced by ethylene in pea epicotyls (Berry et al., 1996) and H-7-sensitive protein kinase(s) was found to be involved in ethylene-induced protein phosphorylation in pea seedlings (Kwak and Lee, 1997). In aerated roots, ethylene increased L_p within 15 min (Fig. 2), similar to the phosphorylation effect observed in tobacco leaves (Raz and Fluhr, 1993). The ethylene-induced increase in L_p of aspen was significantly reversed by the application of STS, which strongly and noncompetitively binds ethylene (Beyer, 1976). Because no changes in L_p were observed in control plants, STS action was likely due to its antagonistic action on ethylene binding. The anionic complex of STS is rapidly transported through plant tissues (Veen, 1983) and can negate the effects of ethylene even after short treatment (Reid et al., 1980). STS inhibited the ethylene binding in carnations (Sisler et al., 1986) and reversed the effects of applied ethylene on root extension growth in lettuce (Lactuca sativa; Abeles and Wydoski, 1987) and on seedling growth of barley (Hordeum vulgare; Locke et al., 2000). In our study, the application of ethylene resulted in an increase in Q_v (Fig. 3) similar to the increase in L_p (Fig. 2). This increase in Q_v in response to ethylene, the decline of the ethylene-induced Q_v by HgCl₂, and the substantial reversion by ME suggest the possible involvement of ethylene in mercury-sensitive processes, particularly the water channel activity, in the enhancement of Q_v by ethylene.

In addition to increased Q_v, both root respiration and g_s increased in hypoxic seedlings after ethylene treatment (Fig. 1C). Respiration rates have been reported to increase in response to ethylene treatment in fruits (Frenkel et al., 1968; McGlasson et al., 1971) and roots (Kahl and Laties, 1989). Ethylene can enhance respiration via the alternative respiration pathways (Esashi et al., 1987) and increase tissue ATP content through mobilization of AMP or ADP (Perl, 1982). It is possible that similar mechanisms and the resulting effect on phosphorylation could also be partly responsible for the increase of Q_v in our experiment. Phosphorylation-induced enhancement of the activity of root water channels could result in an increase in Q_v rates, increase in leaf hydration, and stomatal opening. However, in our study, plants were removed from hypoxic mineral solution with dissolved oxygen levels of <2 mg L⁻¹ and root respiration rates were measured under the oxygen levels of approximately 4 mg L⁻¹ of the nonaerated Hoagland solution. Therefore, the measurements reflected respiration potential under somewhat elevated level of dissolved oxygen rather than the respiration under the prevailing oxygen levels of the hypoxic conditions.

In our study, hypoxic seedlings treated with ethylene for several hours showed a large increase in L_p, which was substantially higher than that observed in roots of aerated seedlings treated with ethylene for several minutes. This might be because of the pronounced responsiveness of the highly physiologically depressed hypoxic roots to ethylene rather than the difference in duration of ethylene treatment. The increased L_p (Fig. 2) and Q_v (Fig. 3) as a result of short-term exposure of roots to ethylene adequately supported the water channel-mediated enhanced L_p in hypoxic seedlings. Because the duration of ethylene treatment for hypoxic seedlings was 12 h, the possibility that ethylene-induced root hair development (Taiz and Zeiger, 1998) could be the reason for the increase in L_p in hypoxic seedlings cannot be entirely ruled out. However, root hair development is often hampered in hydroponically grown plants (Fahn, 1982).

Although dissolved oxygen level of aerated solution was substantially greater than in nonaerated plants, aerated seedlings showed some signs of hypoxia by producing hypertrophic lenticels around the root collar region. In addition, the excised roots of aerated seedlings treated with ethylene in STS experiment and in Q_v experiment were kept in stagnant bathing solution for about an hour before the treatment with ethylene and thus they likely experienced short-term hypoxic condition before ethylene treatment. This could explain why L_p or Q_v of aerated seedlings also showed response to ethylene.

In summary, the results presented in this paper demonstrated an increase in L_p and g_s of hypoxic aspen seedlings after exposing roots to ethylene. We suggest that root water channels likely mediated the ethylene-enhanced root water transport and we discuss the possibility of ethylene effects on phosphorylation of water channel proteins. We interpreted the response of g_s to root-applied ethylene as a result of improved leaf hydration because of the enhancement of Q_v.

MATERIALS AND METHODS

Experimental Conditions and Hypoxic Treatment

Aspen (Populus tremuloides) seedlings were germinated and grown for 6 weeks in styrofoam containers filled with a peat:sand mixture (1:1, v/v) before transferring to aerated solution culture. The roots were gently washed free of soil in cold tap water and the seedlings were transferred to 10-L containers with one-half-strength modified Hoagland solution (Epstein, 1972). Ten containers, each with eight seedlings, were placed in a growth room set to a 16-h photoperiod with photosynthetic photon flux of 300 μmol m⁻² s⁻¹, 22°C/18°C (day/night) temperatures, and a constant relative humidity of approximately 70% (v/v). The seedlings were grown in solution culture for about 3 weeks before experimental treatments and the solution was replaced every 2 weeks.

The seedlings from five randomly picked containers were transferred individually into 0.5-L plastic containers containing one-half-strength Hoagland solution and hypoxia was induced by stopping aeration. The seedlings of other five containers were kept aerated and served as controls. During the hypoxic treatment, the whole root system and a part of the stem 1 cm above the root collar was always kept submerged in the solution. In the aerated containers, the concentration of dissolved oxygen in nutrient solution was always >7 mg L⁻¹, whereas that in the nonaerated containers was <2 mg L⁻¹.

g_s Measurements

Leaf g_s, was measured in hypoxic and control plants at 9 am on d 1, 3, 5, and 10 after the initiation of hypoxic treatment and at 3-h intervals on d 11 after adding ethylene to hypoxic plants. The measurements were carried out with a steady-state porometer (LI-COR, Lincoln, NE) in the same growth chamber where the seedlings were growing. The second fully developed leaf was measured for g_s in each of the five seedlings per treatment (n = 5).

L_p Measurements

Root hydraulic conductance (K_r) was measured for excised root systems of seedlings. A high-pressure flow meter (HPFM; Dynamax Inc., Houston) was used for the measurements as described by Tyree et al. (1995). Each root system was subjected to a pressure increasing from 0 to 0.4 MPa. K_r was the slope of the regression line of the water flow over the applied pressure and expressed in kg MPa⁻¹ s⁻¹. Root volume of each root system was determined from the volume of displaced water and L_p was obtained by dividing the K_r value by root volume and expressed in kg MPa⁻¹ s⁻¹ cm⁻³ root volume. There were five root systems per treatment taken for all measurements (n = 5).

Root Respiration Measurements

Root respiration was measured as oxygen uptake using a Clark-type electrode (Yellow Springs Instruments, Yellow Springs, OH). Respiration rates were determined by placing the root system in an airtight cylinder containing nonaerated one-half-strength Hoagland solution with the initial oxygen level of approximately 4 mg L⁻¹. The bathing solution was kept continuously stirred with a stirring bar during measurements. Oxygen uptake was monitored for 20 min by recording data every 5 min in five root systems per treatment (n = 5). Respiration rate was the average of oxygen uptake over time expressed in μg min⁻¹ cm⁻³ root volume. Mean respiration rate recorded for control root systems was used to normalize the data for each root system of corresponding hypoxic seedlings.

Ethylene Treatment of Hypoxic Seedlings

The individual 0.5-L plastic containers containing hypoxic seedlings were exposed to ethylene at 21 h on d 10, just before the end of the day, 12 h before the measurements on d 11. The roots were sealed in the container with the lower two-thirds of the root system immersed in one-half-strength Hoagland solution and the upper one-third exposed to the air. Ethylene was supplied into the container from the ethylene gas cylinder through a narrow 1-mm diameter tube stretched up to the bottom of the container to a concentration of 20 μL L⁻¹and then the tube was tightly closed. The concentration of the applied ethylene was determined by gas chromatography by comparing the peak area with that produced by pure ethylene standard. Air samples containing ethylene were injected into the 30-m-long, 0.32-mm internal diameter GS-Q column (J&W Scientific, Folsom, CA) and analyzed using a Hewlett-Packard 5890 Series II gas chromatograph (Hewlett-Packard, Mississauga, ON) under the following conditions: oven temperature, 60°C; injector and detector temperatures, 150°C; and carrier gas (helium) linear flow rate, 25 cm s⁻¹.

The seedlings were placed in the growth chamber in the same growth chamber where the seedlings were growing. After 12 h, including an 8-h night period, g_s, L_p, and root respiration were measured in ethylene-treated hypoxic, untreated hypoxic, and aerated seedlings (n = 5) on d 11 at 3-h intervals taking the first measurements at 9 am.

STS Treatment

An excised root system of aerated seedlings was used to record K_r with the HPFM. For ethylene treatment, the excised root system was placed in a plastic container with one-half of the container filled with one-half-strength Hoagland solution. Ethylene gas was supplied into the container following the same procedure as described above and the container was closed airtight. The container with the excised root system exposed to ethylene was then placed in a pressure chamber (PMS Instruments, Corvallis, OR) and pressurized at 0.3 MPa for 10 min. Fifteen minutes after pressurization, K_r of the ethylene-treated root systems was recorded with the HPFM. Then, STS in the form of 0.2 mm silver nitrate and 0.8 mm sodium thiosulphate, in 1:4 (w/v) molar concentration ratio (De Stigter, 1981), was added to the bathing solution and maintained at the room temperature for 4 h before measuring K_r of the root systems that had been exposed to ethylene. At the same time, the root systems that served as controls were also treated with STS and their K_r values were recorded before and after STS treatment as for the ethylene-treated roots.

K_r was measured in seven root systems (n = 7) of each treatment. L_p for individual root system was calculated from the K_r and root volume, and expressed in kg MPa⁻¹ s⁻¹ cm⁻³ root volume. Possible differences between treatment means were explored by paired Student's t test.

Measurements of Q_v in Response to Ethylene and HgCl₂

The steady-state root flow rate (Q_v) was measured following the hydrostatic pressure method (Wan and Zwiazek, 1999; Kamaluddin and Zwiazek, 2001). A 0.25-L glass cuvette containing one-half-strength Hoagland solution was inserted into a pressure chamber (PMS Instruments). The solution was kept continuously stirred during the measurements with a magnetic stirrer. For the measurements, the stem was severed above the collar region and the roots sealed in the pressure chamber. The entire root system was immersed in the solution with the debarked part of the stem protruding through a rubber gasket secured to the lid of the pressure chamber. Chamber pressure was gradually increased to 0.3 MPa and held constant during the measurements. The protruding stem was fitted to a graduated pipette by a short piece of rubber tubing and the water expressed through the stem was collected into the pipette. Root Q_v of the whole root system was monitored over time by recording the volume of sap every 5 min and the results were expressed in μL water min⁻¹ root system⁻¹.

Q_v was measured in the root systems treated with ethylene and/or HgCl₂. Q_v of each root system was recorded for 30 min under constant pressure of 0.3 MPa before treatment. Then, the pressure was released and the roots were treated with ethylene or HgCl₂. Ethylene treatment was given following the same procedure as described for the STS experiment. The ethylene-treated roots were then placed in the pressure chamber and the pressure of 0.3 MPa was restored. The flow was monitored for 30 min after the treatment with ethylene and then the ethylene-treated root system was treated with HgCl₂. For HgCl₂ treatment, the pressure was released and an appropriate amount of concentrated HgCl₂ solution was injected into the bathing solution to achieve 50 μm concentration before pressurizing the roots again to 0.3 MPa. In this way, Q_v of six root systems were monitored for another 1 h. For another set of six root systems, HgCl₂ was added to the bathing solution after measurement of Q_v over the initial 30 min and then monitored for another 1.5 h. Q_v of the HgCl₂-treated roots was measured for another 30 min after adding 20 mm ME to the bathing medium. Q_v was also measured for six control root systems where HgCl₂ or ME was replaced with distilled water and monitored over 2.5 h. Mean Q_v value obtained over the initial 30 min was used to normalize the data for each root system.