Quantitative Estimations of Downward Oxygen Transport from Aerial to Subterranean Parts in Intact Seedlings of Rice and Other Plants

Quantitative estimations of downward oxygen transport from aerial to subterranean parts in intact seedlings were carried out in the present investigation with the respiratory hydrometer specially designed by us for this purpose. The chief object of the investigation is rice, a crop which is notable for its marshy habitat and whose submerged roots are in particular demand of such transport. Some other common plants (wheat, pea, water cress, etc.), either of marshy or of mesophytic habitat, have also been included in the investigation for comparison. Although rice has long been known for its capability of downward oxygen transport, as has often been revealed by various qualitative demonstrations and indirect estimations; yet, data of direct quantitative measurement of the actual amount transported, so far as we are aware, have been very scanty. The few attempts of bringing about such quantitative measurement in an intact plant are made by enclosing its shoot and root in two adjoining compartments respectively, and gas analysis is made on samples taken from each compartment at intervals. The procedure is so elaborate and tedious that estimations on a large scale could not be readily carried out and the results have often been rendered unreliable by mishandling of the plant and air leakage between the compartments. Proposals to the path and mechanism of downward oxygen transport in higher plants have largely been based upon such scanty quantitative approximations and various qualitative observations, and the conclusions derived therefrom are contraversial and far from being convincing. The presentation in this communication of a simple yet accurate experimental method for the quantitative determination of this kind might be opportune and appropriate. The basic principle of the respiratory hydrometer employed in this investigation has been given previously (Lou et al., 1963). Seedlings raised in water culture are inserted into the vessel of the hydrometer (Fig. 1) with its aerial part in the air space above and roots in the water passage below. As the diffusion rate of oxygen in water is about 1/300,000 that in air, the submerged roots of an intact rice seedling practically have their immediate oxygen supply cut off and have to rely upon the oxygen transported from above. Downward oxygen transport in intact seedlings can be easily estimated through the following procedures and the results thus obtained are summarized below: 1. The difference between two consecutive determinations of the oxygen absorbed by the aerial parts of intact seedlings made before and after their roots are severed gives the amount of oxygen transported downwards to roots. For the marshy plant (rice, water cress), it is about 50% (range: 30%–70%) of the total amount absorbed; whereas for ordinary land plants raised in water culture (wheat, pea), it is 20%–30% of the total. 2. The above results are in good agreement with those obtained by determining the respiratory quotients of intact seedlings first in air (e.g.R.Q. ≌ 1 in case of rice seedling) and then with their roots submerged in water (R.Q. ≌ 0.5). The difference between the two consecutive determinations again gives the fraction of oxygen transported downwards. 3. Either by varying the oxygen supply to the aerial part (from 1/4 to twice the oxygen content in air) or by increasing the oxygen consumption of the root through temperature increase or DNP stimulation, the oxygen concentration gradient along the vertical axis of the plant can be steepened or lessened at will. When such experiment is carried out in rice seedlings, the amount of oxygen transported downwards increases with the gradient.     

Path of Downward Oxygen Transport from Aerial to Subterranean Parts in Intact Seedlings of Rice and Other Plants

There are two opposite opinions as regards the mechanism and the path of downward oxygen transport in rice and other higher plants. Van Raalte (1940), Yamada (1952), and others maintain that an oxygen pressure gradient of decreasing magnitude from the stem base down to the root tip exists in the intercellular air spaces, which are interconnected throughout the cortex, and the oxygen transported therein is in free molecular form and moves about by diffusion along its own gradient. Recent diffusion experiments in plants by Barber (1962), employing radioactive O15 as indicator, gave direct confirmation of this hypothesis. The opposite view is held by Brown (1947), Soldatenkov (1963) and others. They consider that the passive diffusion of oxygen along its own gradient is inadequate to account for the actual amount transported downwards. The fact that downward oxygen transport in roots comes almost to a standstill, once the aerial part is removed while the cut end of the short stump is still left in air, casts doubts as to the validity of the diffusion hypothesis; and is in favour of their claim that in addition to, or in placement of, diffusion, active participation of living tissues in shoot is necessary to drive enough oxygen to meet the demand of roots. The oxygen in active transport is no longer in free gaseous state but is in dissolved or combined form (as in peroxides) and moves presumably along the vascular bundles in a way which is hitherto unrevealed but is apparently dependent upon the physiological activity of the conducting tissue. In our previous report (Lou et al 1964), we gave data based on quantitative measurement of the amount of oxygen transported downwards from aerial to submerged parts in intact seedlings with the respiratory hydrometer specially designed for the purpose. In seedlings of marshy plants (e.g. rice), it amounts to about 50% of the total oxygen absorbed by the aerial part; in water cultured seedlings of ordinary land plants (e.g. pea), 20%–30%. By deliberately blocking the alternative paths of oxygen transport in seedlings, one at a time, and measuring the downward oxygen transport accordingly in the same way as before, we should be able to decide which one of the two paths is mainly responsible for the transport. The blocking can be conveniently carried out at the upper end of the radical in a pea (or broadbean) seedling by surgical treatment (see Fig.1); either by ringing off the peripheral cortex where most of the air spaces reside; or by piercing through the central cylinder, within which the vascular bundles are confined. The treated radical is then submerged in water and ready for measurement. Without recourse to surgical treatment and mechanical injury, the air space in the cortex can also be blocked by displacing its air content with water through vacuum infiltration. The present investigation has shown that when the intercellular spaces in the cortex of the radical are blocked either by ringing or by infiltration, the aerial part of the treated seedling absorbs much less oxygen than the control as though its radical were completely severed (Table 2); or, in other words, the downward oxygen transport is effectively stopped by such a means. On the other hand, interruption of vascular bundles in the central cylinder only reduces the amount of oxygen in transport to less than one half, which can be accounted for by the combined effect of the reduced root activity due to shortage of food supply and the unavoidable partial disruption of the peripheral cortex. Besides taking actual measurement, downward oxygen transport in intact pea (or broadbean) seedlings can also be detected by simply noticing the growth rate of its radical. As is shown in this investigation, the radical ceases growing in still water, if the oxygen supply from its aerial part is interrupted. As a result of oxygen deficiency, the radical tip deteriorates in a few days. These effects can be easily realized by ringing off the cortex or by infiltrating its air spaces with water. That the peripheral ringing of the radical does no harm to its growth process is revealed by the fact that if air is bubbled through the water culture steadily, normal growth ensues. The above results leave no doubt that in seedlings of rice, pea, and broadbean, downward oxygen transport mainly takes place in the intercellular spaces in the radical cortex, and seems to have no concern with the activities of vascular bundle and cortex. Although there are evidence that rice roots may actively secrete oxygen in the form of peroxides to its immediate neighborhood (the rhizosphere), the actual amount and the distance traversed in such an active transport however, is very much limited and is insignificant as compared with that taking place in the intercellular spaces.     

Relationship Between Downward Oxygen Transport and Intercellular Spaces in Root Cortex in Water Cultured and Moist Cultured Seedlings

In the present investigation, seedlings of rice, pea, sorghum, and maize are raised both in water culture and moist culture. The former culture is to provide the roots with an oxygen deficient condition; while the latter, a direct access to air. The amount of oxygen transported downwards in the seedlings varies not only with the nature of plants but also with the way how they are raised: More oxygen is transported downwards in marsh plant (rice) than in land plants (pea, sorghum, maize); and, in case the same plant is concerned, more in water cultured seedlings than in moist cultured ones. Downward oxygen transport in the various seedlings is intimately correlated with the relative volume of the intercellular spaces in the root: the more the downward transport, the larger the air spaces in the cortex. The fractional volume of the intercellular spaces in a small plant segment can be conveniently estimated by determining the specific gravities of the fresh turgescent segment before and after it is filled with water by vaccum infiltration. The difference between the two consecutive measurements in specific gravity times 100 gives directly the percentage of the volume occupied by air spaces. When large root segments are used, the relative volume can also be determined by weighing before and after vaccum infiltration. To test whether oxygen diffusion in the intercellular spaces of roots could actually account for its downward transport, a model is built of capillary tubings with dimensions and oxygen pressure gradients similar to those found in roots. The amount of oxygen diffused in such a model is measured with a respiratory hydrometer (see Fig. 1) and fits closely that measured in roots. By comparing the amount of oxygen transported downwards in a seedling with that consumed by its excised roots in air, it can be shown that, in case of rice, it could meet (and at times may even exceed) 100% of that consumed by roots in water cultured seedlings, but is less in moist cultured ones. In land plants (pea, sorghum, and maize), however, the downward oxygen supply is far below its requirement, being 80%–100% in water cultured seedlings and 30%–60% in moist cultured ones. The above results, together with those obtained in previous communications, support the view that adaptation of a plant to flooded condition is primarily achieved by its capacity of providing adequate intercellular spaces for downward oxygen diffusion. The capacity depends not only upon the phylogeny of the plant concerned but also upon its ontogenic development.     

Suppression of gravitropic response of primary roots by submergence

Primary roots of six plant species were placed horizontally either in humid air or under water, and their growth and gravitropic responses were examined. In air, all the roots showed a normal gravitropic curvature. Under water without aeration, roots of rice (Oryza sativa L.), oat (Avena sativa L.), azuki bean (Vigna angularis Ohwi et Ohashi), and cress (Lepidium sativum L.) curved downward at almost same rate as in air, whereas the curvature of roots of maize (Zea mays L.) and pea (Pisum sativum L.) was strongly suppressed. Submergence did not cause a decrease in growth rate of these roots. When roots of maize and pea were placed horizontally under water without aeration and then rotated in three dimensions on a clinostat in air, they showed a significant curvature, suggesting that the step suppressed by submergence is not graviperception but the subsequent signal transmission or differential growth process. Constant bubbling of air through the water partly restored the gravitropic curvature of maize roots and completely restored that of pea roots. The curvature of pea roots was also partly restored by the addition of an inhibitor of ethylene biosynthesis, aminooxyacetic acid. In air, ethylene suppressed the gravitropic curvature of roots of maize and pea. Furthermore, the level of ethylene in the intercellular space of the roots was increased by submergence. These results suggest that the accumulation of ethylene in the tissue is at least partly involved in suppression of transmission of the gravity signal or of differential growth in maize and pea roots under conditions of submergence.Abbreviations AOA aminooxyacetic acid - 3-D three-dimensional Dedicated to Professor Andreas Sievers on the occasion of his retirementWe thank Professor H. Suge and Drs. H. Takahashi and H. Kataoka, Tohoku University and Dr. T. Suzuki, Yamagata University, for helpful suggestions. The present study was supported in part by a Grant for Basic Research in Space Station Utilization from the Institute of Space and Astronautical Science, Japan.     

Graviresponse in higher plants and its regulation in molecular bases: relevance to growth and development, and auxin polar transport in etiolated pea seedlings]

We review the graviresponse under true and simulated microgravity conditions on a clinostat in higher plants, and its regulation in molecular bases, especially on the aspect of auxin polar transport in etiolated pea (Pisum sativum L. cv. Alaska) seedlings which were the plant materials subjected to STS-95 space experiments. True and simulated microgravity conditions substantially affected growth and development in etiolated pea seedlings, especially the direction of growth of stems and roots, resulting in automorphosis. In etiolated pea seedlings grown in space, epicotyls were the most oriented toward the direction far from the cotyledons, and roots grew toward the aerial space of Plant Growth Chamber. Automorphosis observed in space were well simulated by a clinorotation on a 3-dimensional clinostat and also phenocopied by the application of auxin polar transport inhibitors of 2,3,5-triiodobenzoic acid, N-(1-naphtyl)phthalamic acid and 9-hydroxyfluorene-9-carboxylic acid. Judging from the results described above together with the fact that activities of auxin polar transport in epicotyls of etiolated pea seedlings grown in space substantially were reduced, auxin polar transport seems to be closely related to automorphosis. Strenuous efforts to learn in molecular levels how gravity contributes to the auxin polar transport in etiolated pea epicotyls resulted in successful identification of PsPIN2 and PsAUX1 genes located in plasma membrane which products are considered to be putative efflux and influx carriers of auxin, respectively. Based on the results of expression of PsPIN2 and PsAUX1 genes under various gravistimulations, a possible role of PsPIN2 and PsAUX1 genes for auxin polar transport in etiolated pea seedlings will be discussed.     

Influence of submergence on growth of seedlings of Scirpus lacustris and Phragmites australis

• 1 Seeds of Scirpus lacustris and Phragmites australis were germinated in early June, and twenty-four seedlings of each species were subsequently exposed to submerged conditions (eight seedlings at each of the water depths 0.2, 0.4 and 0.8m), in outdoor 500–1 tanks in southern Sweden. Weight and shoot length of the plants were measured in September.
• 2 The Phragmites seedlings did not show any significant growth when submerged. The Scirpus seedlings, however, developed submerged leaves and exhibited considerable submerged growth. One Scirpus plant, in shallow water (0.2m), had developed an aerial shoot by September. Shoot length of the remaining (submerged) Scirpus plants was positively related to plant weight within water depth treatments, and was higher, in relation to plant weight, in deeper water. Mean weight in September of the submerged Scirpus plants decreased with increased water depth.
• 3 In south Swedish lakes with a lowered water table, Scirpus often occupies large areas on the lakeward side of the reed belt, which is generally dominated by Phragmites. The differences between the two species, in performance of submerged seedlings, suggest that this zonation may be created through successful submerged seedling establishment of Scirpus on the lakeward side of Phragmites.

     

Metabolic adaptation to flooding stress in upland and lowland rice seedlings

Ability of metabolic adaptation in upland and lowland rice (Oryza sativa L.) seedlings to flooding stress was compared. Flooding stress increased alcohol dehydrogenase (ADH) activity and ethanol concentration in shoots and roots of the upland and lowland rice seedlings. The difference in ADH activity and ethanol concentration in shoots between the upland and lowland rice was not apparent. However, both ADH activity and ethanol concentration in roots of the lowland rice were 2-fold greater than those in roots of the upland rice, suggesting that flooding-induction of ethanolic fermentation in lowland rice roots may be significantly greater than that in the upland rice roots. Since flooding often causes the anaerobic conditions in rooting zone than aerial part of plants and ethanolic fermentation is essential to survive in the anaerobic conditions, the ability of metabolic adaptation in lowland rice seedlings to flooding stress may be greater than that in upland rice seedlings.     

Inhibitory effects of monoamine oxidase inhibitors on the growth of pea and rice seedlings

Two monoamine oxidase inhibitors of the hydrazine-type, safrazineand nialamide, inhibited growth in seedlings of rice and pea.We demonstrated histochemically that monoamine oxidase is locatedchiefly in sieve tubes and in the epidermis of pea seedling.Activity of this enzyme was high in the apical part of the epicotyl,decreasing toward the base. Inhibition of pea monoamine oxidaseby safrazine and nialamide was observed histochemically andwith an extract from the epicotyl. This supports the hypothesisthat indole-3-acetic acid (IAA) is formed from tryptamine byamine oxidase and that inhibition of this enzyme causes loweringof the auxin level, resulting in growth inhibition. Inhibitionof growth in rice seedlings by safrazine was reversed by theaddition of IAA to the culture medium. (Received May 6, 1970; )     

Antioxidative enzymes in seedlings of Nelumbo nucifera germinated under water

Dry seeds of anoxia-tolerant lotus ( Nelumbo nucifera Gaertn= Nelumbium speciosum Willd.) have green shoots with plastids containing chlorophyll, so photosynthesis starts even in seedlings germinated under water, namely hypoxia. Here we investigated antioxidative enzyme changes in N. nucifera seedlings responding to oxygen deficiency. The activity of superoxide dismutase (SOD; EC 1.15.1.1), dehydroascorbate reductase (DHAR; EC 1.8.5.1) and glutathione reductase (GR; EC 1.6.4.2) were lower in seedlings germinated under water (submerged condition) in darkness (SD seedlings) than those found in seedlings germinated in air and darkness (AD seedlings). In contrast, ascorbate peroxidase (APX; EC 1.11.1.11) activity was higher in SD seedlings and the activity of catalase (EC 1.11.1.6) and monodehydroascorbate reductase (MDAR; EC 1.6.5.4) in SD seedlings was nearly the same as in AD seedlings. When SD seedlings were exposed to air, the activity of SOD, DHAR and GR increased, while the activity of catalase and MDAR decreased. Seven electrophoretically distinct SOD isozymes were detectable in N. nucifera . The levels of plastidic Cu,Zn-SODs and Fe-SOD in SD seedlings were comparable with those found in AD seedlings, which may reflect the maintenance of green plastids in SD seedlings as well as in AD seedlings. These results were substantially different from those previously found in rice seedlings germinated under water.     

Use of X-ray absorption spectroscopy and biochemical techniques to characterize arsenic uptake and reduction in pea (Pisum sativum) plants.

Arsenite (As(III)) and arsenate (As(V)) uptake by peas was investigated using inductively coupled plasma/optical emission spectroscopy (ICP-OES) at pH below 4 and at pH 5.8. Additionally, total amylolitic activity and alpha-amylase (1,4-alpha-d-glucan glucanohydrolase; EC 3.2.1.1) activity was assayed in plants exposed to arsenic treatments. At pH below 4, the uptake for As(III) and As(V) in roots was 137 and 124 mg As kg(-1) dry weight (d wt), respectively. Translocation of arsenic to the aerial part was relatively low ( approximately 5mg As kg(-1) d wt). The uptake for As(III) and As(V) in roots at pH 5.8 was about 43 and 30 mg As kg(-1) d wt, respectively, and translocation of As to the aerial part was not detectable. None of the arsenic treatments affected the total amylolitic activity in roots; however, the shoots from all treatments showed an increase in the total amylolitic activity. Alpha-amylase activity in the pea leaves was not significantly affected by arsenic treatments. X-ray absorption spectroscopy (XAS) studies showed a reduction of As(V) to As(III) in the roots. From linear combination X-ray absorption near edge structure (LC-XANES) fittings, it was determined that arsenic was present as a mixture of As(III) oxide and sulfide in pea roots.     

Transport of Abscisic Acid-2-C-14 in Intact Pea Seedlings

When abscisic acid-2-C-14 (AbA-2-C-14), 1 μg in 5 μl 40% ethanol, is applied to the apical bud of light-grown pea seedlings, C-14 is translocated downwards only in very small amounts and does not enter the root. In contrast to this, C-14 from indoleacetic acid-C-14 (IAA-2-C-14) applied in the same manner is translocated to the root where it accumulates. When AbA-2-C-14 is injected to the stem tissue at the apical bud, more labelled material is transported downwards than after application to the surface. Application of AbA-2-C-14 to an expanded leaf results in considerable accumulation of C-14 in the growing apical parts and in the lateral roots.     

ABA and IAA in rice seedlings under anaerobic conditions

The rice is important in plant science for its ability to germinate and grow with restricted or without oxygen availability. In this work we have investigated the variation of growth substances when anoxia was imposed to rice seedlings previously grown in air. An increase, in all the organs of a seedling and in particular in the fraction released in the medium, was observed for ABA (abscisic acid), PA (phaseic acid) and DPA (dihydrophaseic acid) quantities.Vice versa a reduction of total IAA (indol-3-ylacetic acid) was observed in seedlings. This was accompanied by its accumulation in roots. IAA was poorly released in aerobic conditions and anoxia has not changed this pattern.     

Effects of exposure to humid air on epidermal viability and suberin deposition in maize (Zea mays L.) roots

When the basal zones of 4-d-old hydroponically grown maize ( Zea mays L. cv. Seneca Horizon) roots were exposed to moist air for 2 d, the development of both endodermis and exodermis was affected. In the endodermis, Casparian bands enlarged and more cells developed suberin lamellae. The most striking effect was seen in the exodermis. In submerged controls, only 4% of the cells had Casparian bands, whereas in root regions exposed to air, 93% developed these structures. Similarly, in submerged roots 11% of the exodermal cells had either developing or mature suberin lamellae compared with 92% in the air-treated region. The majority of epidermal cells remained alive in the zone exposed to air. Some cell death had occurred earlier in the experiment when the seedlings were transferred from vermiculite to hydroponic culture. The precise stimulus(i) associated with the air treatment which led to accelerated development in both endodermis and exodermis is as yet unknown.     

Chilling Sensitivity of Photosynthetic Oil-Seedlings: I COTTON SUNFLOWER

Despite the high probability that sensitive post-emergent seedlingswill be exposed to suboptimal temperatures which significantlyaffect subsequent development and yield, growers of long-season,indeterminate crops must rely upon empirically determined ‘earliestplanting dates’ Most ‘chilling-stress’ studieshave dealt, not with photosynthetic seedlings, but rather withthe effect of low, non-freezing temperatures (< 10 ?) upongerminating seeds and pre-emergent seedlings. A photosyntheticseedling growth system was used to monitor the effects of temperaturesfrom 10 to 35? upon the roots and aerial portions of chilling-sensitivecotton and relatively chilling-resistant sunflower oil-seedlings.Length measurements of cotton seedlings were too variable tobe reliable indicators of temperature treatment effects, butroot and shoot fresh weights could be used as non-destructivemeasurements of differences in root and shoot temperature responsesin both cotton and sunflower seedlings. The fresh weights wereindicative of the relative water status of seedling roots andshoots, including that of seedlings returned to 30? after exposureto other temperatures. Growth of both cotton and sunflower seedlingswas inhibited to some degree at non-optimal temperatures andthe capacities of the roots and shoots to return to normal waterstatus, as indicated by fresh weights and relative water contents,was correlated with sensitivity to suboptimal temperatures Key words: Cotton, sunflower, temperature, water status     

Ethylene enhances water transport in hypoxic aspen

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 microM HgCl(2) 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.     

Growth of submerged mycelia of Aspergillus kawachii in solid-state culture

Submerged mycelial growth of Aspergillus kawachii IFO4308 in solid-state culture (SSC) was studied. From the result of Northern blot analysis, acid-stable α-amylase was found to be produced mainly by the submerged mycelia rather than the aerial mycelia. The submerged mycelia showed better growth in SSC using rice as the solid substrate (koji) than in agar plate culture in spite of low concentrations of dissolved oxygen in koji. Good growth in SSC suggested the existence of an effective oxygen transfer mechanism in koji which governed the mycelial growth. When koji was submerged in water, small bubbles were generated. This phenomenon indicated the formation of vacant spaces in koji during SSC. The submerged mycelia showed better growth in the koji having a larger number of vacant spaces. Considering these facts it was concluded that the vacant spaces participate in effecting an oxygen transfer mechanism in koji as air vents because the diffusivity of oxygen in an air is larger than in koji itself.     

Respiratory Properties of Mitochondria from Rice Seedlings Germinated under Water and Their Changes during Air Adaptation

Respiratory activities were compared among rice seedlings germinated in air for 6 days (aerobic seedlings), those germinated under water for 5 days (submerged seedlings), and those grown in air for 1 day after 5 days' submerged germination (air-adapted seedlings). The respiratory activity of the submerged seedlings increased rapidly on transfer to air and reached a plateau at 16 hours in air. Respiration of the submerged seedlings was as sensitive to cyanide as those of aerobic and air-adapted seedlings. 2,4-Dinitrophenol had no effect on the respiration of the submerged seedlings, but stimulated those of the other two types of seedlings. Mitochondria from three types of seedlings did not differ in the ADP/O ratio and the respiratory control ratio (RCR) when succinate was oxidized. However, mitochondria from submerged seedlings (submerged mitochondria) showed poor RCR of about unity when malate was oxidized. Both the rate of succinate oxidation and succinate dehydrogenase activity were low in submerged mitochondria, but increased during air adaptation. Although submerged mitochondria oxidized malate very slowly, this activity increased after exposure to air without any increase in malate dehydrogenase activity. When NAD⁺ was added to submerged mitochondria, oxidation of malate was restored to the level of the aerobic controls. Addition of NAD⁺ enhanced the state 3 rate in submerged mitochondria, and RCR recovered to nearly the same value as that of the aerobic controls. Similar effects of NAD⁺ on 2-oxoglutarate oxidation were observed. All these defects in submerged mitochondria were repaired during air adaptation. These results suggest that NAD⁺-linked substrate oxidation was low in submerged mitochondria because of NAD⁺ deficiency, and that the oxidation increased with an increasing level of NAD⁺ during air adaptation.     

The tropic response of plant roots to oxygen: oxytropism in Pisum sativum L.

Plant roots are known to orient growth through the soil by gravitropism, hydrotropism, and thigmotropism. Recent observations of plant roots that developed in a microgravity environment in space suggested that plant roots may also orient their growth toward oxygen (oxytropism). Using garden pea (Pisum sativum L. cv. Weibul's Apollo) and an agravitropic mutant (cv. Ageotropum), root oxytropism was studied in the controlled environment of a microrhizotron. A series of channels in the microrhizotron allowed establishment of an oxygen gradient of 0.8 mmol · mol⁻¹ · mm⁻¹. Curvature of seedling roots was determined prior to freezing the roots for subsequent spectrophotometric determinations of alcohol dehydrogenase activity. Oxytropic curvature was observed all along the gradient in both cultivars of pea. The normal gravitropic cultivar showed a maximal curvature of 45° after 48 h, while the agravitropic mutant curved to 90°. In each cultivar, the amount of curvature declined as the oxygen concentration decreased, and was linearly related to the root elongation rate. Since oxytropic curvature occurred in roots exposed to oxygen concentrations that were not low enough to induce the hypoxically responsive protein alcohol dehydrogenase, we suspect that the oxygen sensor associated with oxytropism does not control the induction of hypoxic metabolism. Our results indicate that oxygen can play a critical role in determining root orientation as well as impacting root metabolic status. Oxytropism allows roots to avoid oxygen-deprived soil strata and may also be the basis of an auto-avoidance mechanism, decreasing the competition between roots for water and nutrients as well as oxygen. Received: 14 January 1998 / Accepted: 10 February 1998     

Maximum axial and radial growth pressures of plant roots

Summary The axial root growth force exerted by seedlings of pea (Pisum sativum cv. Greenfeast), cotton (Gossypium hirsutum cv. Sicot 3) and sunflower (Helianthus annuus cv. Hysun) was measured. Effects of different seedling age and different batches of seeds on axial root growth pressure were investigated. Mean values of the maximum axial root growth pressure (P_a) estimated from the maximum axial root growth force (F_max) and root diameter were 497, 289, and 238 kPa respectively for pea, cotton and sunflower seedlings of same size. P_a and F_max were significantly influenced by seedling age and for pea seedlings of same age they varied with the seed batch. A new technique was developed for estimating radial root growth pressure and was tested on pea seedlings. Each pea root was confined both in the axial and radial directions in a cylindrical chalk sample at a constant water potential. The roots exerted radial stress which caused tensile failure in a proportion of the chalks. The measurement of tensile strength of duplicate chalks enabled estimation of the maximum radial pressures exerted by the roots. The maximum axial and radial root growth pressures were of comparable magnitude.