Changes in growth and water-soluble solute concentrations in Sorghum bicolor stressed with sodium and potassium salts

Sorghum bicolor L. Moench, RS 610, was grown in liquid media salinized with NaCl, KCl, Na₂SO₄, K₂SO₄ or with variable mixtures of either NaCl/KCl or Na₂SO₄/K₂SO₄ at osmotic potentials ranging from 0 to -0.8 MPa. The purpose was to study the effects of different types and degrees of salinity in growth media on growth and solute accumulation. In 14-day-old plants the severity of leaf growth inhibition at any one level of osmotic potential in the medium increased according to the following order: NaCl < Na₂SO₄ < KCl = K₂SO₄. Inhibition of growth by mixtures of Na⁺ and K⁺ salts was the same as by K⁺ salts alone. Roots responded differently. Root growth was not affected by Na⁺ salts in the range of 0 to -0.2 MPa while it was stimulated by K⁺ salts. The major cation of leaves was K⁺ because S. bicolor is a Na⁺-excluder, while Na⁺ was the major cation in roots except at low Na⁺/K⁺ ratios in media. Anions increased in tissues linearly in relation to total monovalent cation, but not with a constant anion/cation ratio. This ratio increased as the cation concentrations in tissues increased. Sucrose in leaf tissue increased 75 fold in Chloride-plants (plants growing in media in which the only anion of the salinizing salts was Cl^?) and 50 fold in Sulphate-plants (the only anion of the salinizing salts was SO₄^2-). Proline increased 60 and 18 fold in Chloride- and Sulphate-plants, respectively, as growth media potentials decreased from 0 to -0.8 MPa. The concentrations of both sucrose and proline were directly proportional to the amount of total monovalent cation in the tissue. Sucrose concentrations began increasing when total monovalent cations exceeded 100 μmol (g fresh weight)^?1 (the monovalent cation level in non-stressed plants), but proline did not start accumulating until monovalent cation concentrations exceeded 200 μmol (g fresh weight)^?1. Therefore, sucrose seemed to be the solute used for osmotic adjustment under mild conditions of saline stress while proline was involved in osmotic adjustment under more severe conditions of stress. Concentrations of inorganic phosphate, glucose, fructose, total amino acids and malic acid fluctuated in both roots and leaves in patterns that could be somewhat correlated with saline stress and, sometimes, with particular salts in growth media. However, the changes measured were too small (at most a 2–3 fold increase) to be of importance in osmotic adjustment.     

Growth and solute accumulation in 3-week-old seedlings of Agropyron elongatiun stressed with sodium and potassium salts

Agropyron elongatum [Host. (Beauv.)] [^cv. Arizona Glendale, was grown in liquid medium salinized with either NaCl, KCI, or a 50:50 mixture of these two salts at osmotic potentials ranging from 0 to –1.6 MPa. The amount of growth in 21 days was measured, and extracts were made of the shoots at this time. The extracts were assayed for low-molecular-weight organic compounds (glucose, fructose, sucrose, be-taine, proline) and inorganic solutes (Na⁺, K⁺, Cl^?, P.). The purpose was to determine if there was any correlation between the harmful effect of salinity on growth and the concentrations of solutes in tissues. Growth inhibition of A. elongatum was roughly proportional to the osmotic potential of the growth medium and was independent of the ionic composition of the salinizing salts. Total monovalent cation (the sum of Na⁺ and K⁺) concentrations and the ratio of these two cations in leaves were mainly a function of the ionic compostion of the salt in growth media, and, to a lesser degree, of osmotic potentials. F At an osmotic potential of –0.2 MPa, total monovalent cation in leaves was the same as in non-stressed plants. However, if the salinizing salt contained NaCl, there was an increase in foliar Na⁺ with a balancing decrease in K⁺. At stress levels between –0.4 and –1,6 MPa, and, if the media were salinized with either 100% NaCl or a 50:50 mixture of NaCl and KCI, total monovalent cation concentrations remained constant at a value that was twice that in non-stressed plants. Although total monovalent cation concentrations were equal in plants grown under these two salinity conditions, the K⁺/Na⁺ ratios shifted from a value of 1:2 in plants grown in 100% NaCl to 3:1 in plants subjected to the 50:50 mixture. If 100% KCI was used to salinize media, total monovalent cation was 80% of its concentration in NaCl-treated plants in the range of –0.4 to -1.2 MPa. At –1.6 MPa due to 100% KCI, total monovalent cation was double that in plants subjected to -0.4 MPa. In the range of osmotic potentials from–0.2 to –1.2 MPa, the chloride:cation ratio was 1:2. At –1.6 MPa the ratio changed to 3:4. Proline started accumulating in leaves of A. elongatum when the tissue concentration of total monovalent cation exceeded 200 μ (g fresh weight)^?1. Above this threshold value of total monovalent cation, the proline concentration of leaves was 6% of the amount of total monovalent cation that exceeded 200 umol (g fresh weight)¹.     

Solute adjustments in leaves of two species of wheat at two different stages of growth in response to salinity

Changes in leaf solute concentrations in response to salinity were measured at two growth stages in two species of wheat, Triticum turgidum L. cv. Aldura (Durum group) and Triticum aestivum L., cv. Probred that differed in their salt tolerances. Both species at 55 days of age were Na⁺-excluders, but the concentration of Na⁺ was 10 times higher in T. turgidum than T. aestivum at low to moderate levels of stress. The ratio then decreased until it was 2:1 at – 1.2 MPa. In T. turgidum, K⁺ concentrations decreased with increasing Na⁺ concentrations so that the sum of the two cations remained constant at all stress levels, but in T. aestivum K⁺ decreased more rapidly than Na⁺ increased. In both species growing in media at 0 to –0.6 MPa, the amounts of Mg²⁺ and Ca²⁺ in 55-day-old plants that could be extracted with hot water were below 0.1 mmol (g dry weight)^?1. Then, as osmotic potentials of media decreased further, hot water-extractable Ca²⁺ increased greatly until, at – 1.2 MPa, Ca²⁺ concentrations were almost equal to the sum of Na⁺ and K⁺. In the range of 0 to –1.0 MPa, the ratio of Cl^? to total cationic charge remained constant at 1:6 in T. aestivum and 1:2 in T. turgidum. However, at – 1.2 MPa, the ratio in both species had changed to 2:3. Sucrose and betaine concentrations were 4 and 48 μmol (g dry weight)^?1, respectively, in non-stressed plants of both species. At – 1.2 MPa, sucrose had increased 30-fold but betaine had increased only 2.5-fold. Proline increased exponentially relative to foliar Na⁺ in T. turgidum. In T. aestivum only plants grown at –1.2 MPa contained sufficient Na⁺ to stimulate the accumulation of proline. Although the quantities of the solutes in leaves of non-stressed 96-day-old plants differed from those in non-stressed younger plants, the patterns of change of organic solutes as the older plants were subjected to increasing saline stresses were the same as in younger plants with the exception of sucrose. Sucrose concentrations were much higher in leaves of non-stressed older plants and this sugar first increased and then decreased with decreasing osmotic potentials of media.     

Differential effects of Na+, Mg2+, K+, Ca2+ and osmotic stress on the wild type and the NaCl-tolerant mutants stl1 and stl2 of Ceratopteris richardii

In order to identify physiological components that contribute to salinity tolerance, we compared the effects of Na⁺, Mg²⁺ and K⁺ salts (NaCl, Na₂SO₄, MgCl₂, MgSO₄, KCl and K₂SO₄), Ca₂₊ (CaSO₄), mannitol and melibiose on the wild type and the single-gene NaCl-tolerant mutants stl1 and stl2 of Ceratopteris richardii. Compared with gametophytic growth of the wild type, stl2 showed a low level of tolerance that was restricted to Na⁺ salts and osmotic stress. stl2 exhibited high tolerance to both Na⁺ and Mg²⁺ salts, as well as to osmotic stress. In response to short-term exposure (3 d) to NaCl, accumulation of K⁺ and Na⁺ was similar in the wild type and stl1. In contrast, stl2 accumulated higher levels of K⁺ and lower levels of Na⁺. Ca²⁺ supplementation (1.0 mol m^?3) ameliorated growth inhibition by Na⁺ and Mg²⁺ stress in wild type and stll, but not in stl2. In addition, under Na⁺ stress (175 mol m^?3) wild-type, stll and stl2 gametopbytes maintained higher tissue levels of K⁺ and lower levels of Na⁺ when supplemented with Ca²⁺ (1.0 mol m^?3). stl2 gametophytes were extremely sensitive to K⁺ supplementation. Growth of stl2 was greater than or equal to that of the wild type at trace concentrations of K⁺ but decreased substantially with increasing K⁺ concentration. Supplementation with K⁺ from 0 to 1.85 mol m^?3 alleviated some of the inhibition by 75 mol m^?3 NaCl in the wild type and in stl1. In stl2, growth at 75 mol m^?3 NaCl was similar at 0 and 1.85 mol m^?3 K⁺ supplementation. Although K⁺ supplementation above 1.85 mol m^?3 did not alleviate inhibition of growth by Na⁺ in any genotype, stl2 maintained greater relative tolerance to NaCl at all K⁺ concentrations tested.     

Influence of physical factors on the growth of insect cells in vitro

Summary The tolerances of a cell line (IMC-HZ-1) from a moth,Heliothis zea, for the monovalent cations Na⁺ and K⁺ were defined. Cells shifted to media containing more than 70mm of K⁺ showed decreased growth rates. No evidence was obtained for Na⁺ toxicity. The osmotic pressure tolerances were influenced by the K⁺ concentration of the medium. The richer the medium was in K⁺, the narrower was the spectrum of osmotic pressure tolerance. Once the limit of K⁺ tolerance was exceeded, the rate of decline of growth was linear with respect to further increases in K⁺. This rate of decline was independent of osmotic pressure. The initial responses of cells during one subculture (2 to 4 population doublings) in media differing from the standard medium (used to maintain the cell line) were not reliable indicators of the growth potential of the cells. Continued subculture in such media resulted in an upward trend in population growth rates in most cases. This investigation was supported by U. S. Public Health Service Research Grant no. AI 09914 from the National Institute of Allergy and Infectious Diseases. This is Paper no. 8637, Scientific Journal Series, Minnesota Agricultural Experiment Station. The material is part of the dissertation of T. J. K. presented for the Ph.D. degree at the University of Minnesota.     

Hormones-induced modifications in the response of wheat flag leaf to NaCl

A field experiment was carried out to investigate the effects of presoaking the wheat grains (Triticum aestivum L.) in 33 or 66 mM NaCl and indolyl-3-acetic acid (IAA at 50 g m⁻³), gibberellic acid (GA₃ at 100 g m⁻³) or kinetin (100 g m⁻³) on some tolerance criteria in wheat flag leaf at different stages of development. At various stages of flag leaf development pretreatment with 33 or 66 mM NaCl decreased degree of succulence (particularly 66 mM), relative growth rate, net assimilation rate, relative water content, K⁺ content and K⁺/Na⁺ ratio and at the same time induced accumulation of abscisic acid and Na⁺. In the majority of cases grain pretreatment with GA₃ or kinetin and to a lesser extent with IAA alleviated either partially or completely the deleterious effect of salinity on the above mentioned parameters.     

Effects of salinity on uptake and distribution of Na+, Cl- and K+ in two wheat cultivars

Plants of two wheat (Triticum aestivum L.) cultivars differing in salt tolerance were grown in sand with nutrient solutions. 35-d-old plants were subjected to 5 levels of salinity created by adding NaCl, CaCl₂ and Na₂SO₄. Growth reduction caused by salinity was accompanied by increased Na⁺ and Cl^- concentrations, Na⁺/K⁺ ratio, and decreased concentration of K⁺. The salt tolerant cv. Kharchia 65 showed better ionic regulation. Salinity up to 15.7 dS m^-1 induced increased uptake of Na⁺ and Cl^- but higher levels of salinity were not accompanied by further increase in uptake of these ions. Observed increases in Na⁺ and Cl^- concentrations at higher salinities seemed to be the consequence of reduction in growth. Uptake of K⁺ was decreased; more in salt sensitive cultivar. This was also accompanied by differences in its distribution.     

Salt-tolerance in plants. II. In vitro translation of m-RNAs from salt-tolerant and salt-sensitive plants on wheat germ ribosomes. Responses to ions and compatible organic solutes

Abstract Messenger RNA from salt-sensitive and salt-tolerant plants Triticum aestivum. Beta vulgaris, Pisum sativum, Chenopodium album and Atriplex nummularia was translated in vitro in a wheatgerm translation system. The optimal monovalent and divalent ion concentrations for translation were independent of the salt tolerance of the plants from which the m-RNAs were derived. Translation was optimal in 100 120 mol m⁻³ potassium acetate and 1.5–2.0 mol m⁻³ Mg²⁺. Substitution of Na⁺ for K⁺, or of Cl⁻ for acetate, was inhibitory. The pattern of polypeptides synthesized from cytoplasmic m-RNAs of salt-sensitive and salt-tolerant plants remained constant in all the conditions examined. The effects of adding the ‘compatible' organic solutes glycine-betaine and mannitol were examined in the wheat-germ system primed with RNA from the leaves of Triticum aestivum or Beta vulgaris. The rate of translation, the optimum ionic concentrations and the distribution of polypeptide products were maintained in organic solute concentrations of up to 500 mol m⁻³. Proline above 300 mol m⁻³ and surcose above 100 mol m⁻³ did inhibit translation. The results indicate that translation in plants is unlikely in cytoplasmic K⁺ concentrations exceeding 180 mol m⁻³, but would proceed in the presence of up to 500 mol m⁻³ mannitol or glyinebetaine, or of up to 300 mol m⁻³ proline.     

Salt-tolerance in plants. I. Ions, compatible organic solutes and the stability of plant ribosomes

Abstract Polysomes and ribosomes recovered from a number of plant species were tested for stability when incubated at 25°C in salt solutions in the absence of ATP and initiation factors. Stability was assessed by sucrose density gradient analysis. The stability was inversely proportional to salt concentrations above 125 mol m⁻³ KCl. Polysomes were less stable in the presence of Na⁺ than K⁺ salts, and were much less stable in Cl⁻ than in acetate salts. Polysomes from Triticum aestivum. Hordeum vulgare, Capsicum annuum, Helianthus annuus. Pisum sativum, Atriplex nummularia, Beta vulgaris, Cladophora sp., Enteromorpha sp. and Corallina cuvieri were similarly sensitive to KCl. Polysomes from Ulva lactuca were more sensitive than the other species. Cytoplasmic and plastid polysomes from T. aestivum were similarly unstable in 500 mol m⁻³ KCl. Unprogrammed ribosomal subunit couples from T. aestivum, B. vulgaris and U. lactuca showed Mg²⁺-dependent conformational instability and dissociation in KCl. Slight differences in ribosomal stability were observed between species, but these were unrelated to the salt tolerances of the plants. The ‘compatible’ organic solutes, glycinebetaine and proline, failed to reduce ion-induced instability. Ribosome yield and polysome profiles were similar in leaves of B. vulgaris containing significantly different levels of both Na⁺ and Cl⁻ after growth in media containing 50 or 200 mol m⁻³ NaCl. The results are consistent with the hypothesis that plants maintain a cytoplasmic solute environment that is compatible with ribosomal stability.     

Osmotic adaptation in halotolerant yeast, Debaryomyces nepalensis NCYC 3413: role of osmolytes and cation transport

Debaryomyces nepalensis NCYC 3413, a food spoiling yeast isolated from rotten apple, has been previously demonstrated as halotolerant yeast. In the present study, we assessed its growth, change in cell size, and measured the intracellular polyol and cations (Na⁺ or K⁺) accumulated during growth in the absence and presence of different concentrations of salts (NaCl and KCl). Cells could tolerate 2 M NaCl and KCl in defined medium. Scanning electron microscopic results showed linear decrease in mean cell diameter with increase in medium salinity. Cells accumulated high amounts of K⁺ during growth at high concentrations of KCl. However, it accumulated low amounts of Na⁺ and high amounts of K⁺ when grown in the presence of NaCl. Cells grown in the absence of salt showed rapid influx of Na⁺/K⁺ on incubation with high salt. On incubation with 2 M KCl, cells grown at 2 M NaCl showed an immediate efflux of Na⁺ and rapid uptake of K⁺ and vice versa. To withstand the salt stress, osmotic adjustment of intracellular cation was accompanied by intracellular accumulation of polyol (glycerol, arabitol, and sorbitol). Based on our result, we hypothesize that there exists a balanced efflux and synthesis of osmolytes when D. nepalensis was exposed to hypoosmotic and hyperosmotic stress conditions, respectively. Our findings suggest that D. nepalensis is an Na⁺ excluder yeast and it has an efficient transport system for sodium extrusion.     

Effects of buffer capacity on growth,photosynthesis, and solute accumulation of a glycophyte (wheat) and a halophyte (<Emphasis Type="Italic">Chloris virgata</Emphasis>)

Two species with different resistances to alkaline pH, the glycophylic Triticum aestivum (wheat) and the halophilic Chloris virgata, were chosen as test organisms. The salt-alkaline (SA) mixed stress conditions with different buffer capacities (BC) but with the same salt molarities and pH were established by mixing neutral (NaCl, Na₂SO₄), and alkaline salts (NaHCO₃ and Na₂CO₃) in various proportions. Growth, photosynthetic characteristics, and solute accumulation of the seedlings were monitored to test the validity of BC as a decisive index of alkali-stress (AS) intensity in SA mixed stress. At the same salinities and pHs, the relative growth rate, the content of photosynthetic pigments, and net photosynthetic rates of wheat and C. virgata decreased, while Na⁺ content and Na⁺/K⁺ ratios in shoots increased with increasing BC. Hence BC was a true measure of AS intensity at mixed SA stress and the alkali-resistance mechanism of plants was easy to interpret. BC of soil solution is an important parameter for estimating the alkalization degree of salt-alkalized soil.     

The Usage of Plasmalemmal Vesicles Inverted by Brij 58 Treatment for Studying Processes,which Occur on the Cytosolic Membrane Surface

We studied the possible use of the detergent Brij 58 in physiological experiments for the reorientation of right-side-out plasmalemmal vesicles, which were isolated from wheat (Triticum aestivum L.) coleoptiles. The activities of K⁺, Mg²⁺-ATPase and the ATP-dependent H⁺-potential were higher in Brij 58-treated vesicles, whereas membrane permeability for K⁺ and Na⁺ remained unchanged. Brij 58 did not suppress the ATP-dependent IAA transport into vesicles and RNA polymerase II activation by IAA–protein plasmalemmal complexes in the system of isolated nuclei. The conclusion was that, using Brij 58, we could obtain the plasmalemmal fraction, which consisted almost completely of closed inverted vesicles. These vesicles can be applied for the in vitro study of the processes, which occur on the cytosolic plasmalemmal surface.     

Responses of salt-tolerant and intolerant wheat genotypes to sodium chloride: Photosynthesis,antioxidants activities,and yield

Physiological responses of two wheat (Triticum aestivum L.) genotypes (salt-tolerant DK961 and salt-sensitive JN17) to increased salt concentrations (50, 100, 150 mM NaCl: NaCl⁵⁰, NaCl¹⁰⁰, NaCl¹⁵⁰) were studied. Photosynthetic capacity, irradiance response curves, contents of soluble sugars, proteins, and chlorophyll (Chl), K⁺/Na⁺ ratio, and activities of antioxidant enzymes (superoxide dismutase, peroxidase, and catalase) in flag leaves were measured on 7 d after anthesis. In control (NaCl⁰) plants, non-significant (p>0.05) differences were found in gas exchange and saturation irradiance (SI) between salt-tolerant (ST) and salt-sensitive (SS) wheat genotypes. However, we found higher soluble sugar and protein contents, K⁺/Na⁺ ratio, and antioxidant enzyme activities, but lower Chl content and yield in ST wheat. Salinity stresses remarkably increased soluble sugar and protein contents and the antioxidant activities, but decreased K⁺/Na⁺ ratio, Chl contents, SI, photosynthetic capacities, and yield, the extent being considerably larger in JN17 than DK961. Although the soluble sugar and protein contents and the antioxidant activities of JN17 elevated more evidently under salt stresses, those variables never reached the high levels of DK961. The antioxidant enzyme activities of SS wheat increased in NaCl⁵⁰ and NaCl¹⁰⁰, but decreased rapidly when the NaCl concentration reached 150 mM. Thus the ST wheat could maintain higher grain yield than the SS one by remaining higher osmoregulation and antioxidative abilities, which led to higher photosynthetic capacity. Hence the ST wheat could harmonize the relationship between CO₂ assimilation (source) and the grain yield (sink) under the experimental conditions.     

The Effect of Different Salts of Sodium and Potassium on the Accumulation of Glycinebetaine in Atriplex Prostrata

Atriplex prostrata was grown for one month in nutrient solutions with NaCl, KCl, Na₂SO₄, and K₂SO₄ (at osmotic potentials of 0, –0.75, –1.00, and –1.50 MPa). Plants treated with K₂SO₄ had less glycinebetaine at –1.0 and –1.50 MPa than those treated with Na⁺ salts, probably due to the inhibitory effects of K⁺ on glycinebetaine accumulation.     

ATP-dependent Ca2+ transport in wheat root plasma membrane vesicles

Plasma membrane preparations of high purity were obtained from roots of dark-grown wheat (Triticum aestivum L. cv. Drabant) by aqueous polymer two-phase partitioning. These preparations mainly contained sealed, right-side-out vesicles (ca 90% exposing the original outside out). By subjecting the preparations to 4 freeze/thaw cycles the proportion of sealed, inside-out (cytoplasmic side out) vesicles increased to ca 30%. Inside-out and right-side-out plasma membrane vesicles were then separated by partitioning the freeze/thawed plasma membranes in another aqueous polymer two-phase system. In this way, highly purified, sealed, inside-out (>60% inside-out) vesicles were isolated and subsequently used for characterization of the Ca²⁺ transport system in the wheat plasma membrane. The capacity for ⁴⁵Ca²⁺ accumulation, nonlatent ATPase activity and proton pumping (the latter two markers for inside-out plasma membrane vesicles) were all enriched in the inside-out vesicle fraction as compared to the right-side-out fraction. This confirms that the ATP-binding site of the ⁴⁵Ca²⁺ transport system, similar to the H⁺-ATPase, is located on the inner cytoplasmic surface of the plant plasma membrane. The ⁴⁵Ca²⁺ uptake was MgATP-dependent with an apparent K_m for ATP of 0.1 mM and a high affinity for Ca²⁺ [K_m(Ca²⁺/EGTA) = 3 μM]. The pH optimum was at 7.4–7.8. ATP was the preferred nucleotide substrate with ITP and GTP giving activities of 30–40% of the ⁴⁵Ca²⁺ uptake seen with ATP. The ⁴⁵Ca²⁺ uptake was stimulated by monovalent cations; K^? and Na⁺ being equally efficient. Vanadate inhibited the ⁴⁵Ca²⁺ accumulation with half-maximal inhibitions at 72, 57 and 2 μM for basal, total (with KCI) and net K⁺-stimulated uptake, respectively. The system was also highly sensitive to erythrosin B with half-maximal inhibition at 25 nM and total inhibition at 1μM. Our results demonstrate the presence of a primary Ca²⁺ transport ATPase in the plasma membrane of wheat roots. The enzyme is likely to be involved in mediating active efflux (ATP-binding sites on the cytoplasmic side) to the plant cell exterior to maintain resting levels of cytoplasmic free Ca²⁺ within the cell.     

Effects of interrupted K+ supply on growth and uptake of K+, Ca2+, Mg2+ and Na+ in spring wheat

Effects of interrupted K⁺ supply on different parameters of growth and mineral cation nutrition were evaluated for spring wheat (Triticum aestivum L. cv. Svenno). K⁺ (2.0 mM) was supplied to the plants during different periods in an otherwise complete nutrient solution. Shoot growth was reduced before root growth after interruption in K⁺ supply. Root structure was greatly affected by the length of the period in K⁺ -free nutrient solution. Root length was minimal, and root branching was maximal within a narrow range of K⁺ status of the roots. This range corresponded to cultivation for the last 1 to 3 days, of 11 in total, in K⁺ -free nutrient solution, or to continuous cultivation in solution containing 0.5 to 2 mM K⁺. In comparison, both higher and lower internal/external K⁺ concentrations had inhibitory effects on root branching. However, the differing root morphology probably had no significant influence on the magnitude of Ca²⁺, Mg²⁺ and Na⁺ uptake. Uptake of Ca²⁺ and especially Mg²⁺ significantly increased after K⁺ interruption, while Na⁺ uptake was constant in the roots and slowly increased in the shoots. The two divalent cations could replace K⁺ in the cells and maintain electroneutrality down to a certain minimal range of K⁺ concentrations. This range was significantly higher in the shoot [110 to 140 μmol (g fresh weight)^?1] than in the root [20 to 30 μmol (g fresh weight)^?1]. It is suggested that the critical K⁺ values are a measure of the minimal amount of K⁺ that must be present for physiological activity in the cells. At the critical levels, K⁺ (⁸⁶Rb) influx and Ca²⁺ and Mg²⁺ concentrations were maximal. Below the critical K⁺ values, growth was reduced, and Ca²⁺ and Mg²⁺ could no longer substitute for K⁺ for electrostatic balance. In a short-term experiment, the ability of Ca²⁺ to compete with K⁺ in maintaining electroneutrality in the cells was studied in wheat seedlings with different K⁺ status. The results indicate that K⁺, which was taken up actively and fastest at the external K⁺ concentration used (2.0 mM), partly determines the size of Ca²⁺ influx.     

Vigor and salt tolerance in 3 lines of tall wheatgrass

The F₁ progeny of the cross of two salt-tolerant lines of Thinopyrum elongatum [Host] D. R. Dewey grew better than either parent under non-saline and saline growth conditions. Under non-saline conditions, the hybrid produced 1.8 times as much vegetative tissue as one parent and 3.2 times more than the other parent in the same length of time. The relative growth rates of the 2 parental lines decreased equally as media osmotic potentials decreased. The relative growth rate of the hybrid did not decrease as rapidly as that of the parents; therefore, it was concluded that the greater growth of the hybrid was due to increased salt tolerance. Carbohydrate reserves and water-soluble solutes believed to be involved in osmotic adjustment were assayed to determine if there were any differences between the hybrid and its parents in their abilities to accumulate these compounds. The concentrations of these constituents were measured at dawn and at dusk of the same day in plants grown in media at osmotic potentials ranging from –0.1 to –1.2 MPa. There were no differences in pool sizes of the organic compounds in the 3 lines. Starch increased 10–40 fold in leaves from dawn to dusk and sucrose increased 100-fold. However, this pattern was unaffected by salinity. Conversely, betaine concentrations increased with increasing salinity but were the same at dawn and dusk. Na⁺ and K⁺ were affected by both light and salinity. Cl was one-half (Na⁺+ K⁺) on a molar basis under all conditions. Proline accumulated when (Na⁺+ K⁺) exceeded 200 μmol (g fresh weight)^?1. Since this amount of (Na⁺+ K⁺) existed only in tissues harvested at dusk from severely saline-stressed plants, only leaves from such plants harvested at dusk contained proline.     

Ion movements induced by transcellular osmosis inNitella flexilis

Summary Movements of K⁺, Na⁺, and Cl^}- ions during transcellular osmosis were studied in internodal cells ofNitella flexilis. Much K⁺ was released from the endosmotic cell part, but only a little from the exosmotic cell part. The amount of K⁺ released depended on the osmotic gradient driving transcellular osmosis. Movement of Na⁺ was hardly detected. Cl^}- was released in nearly the same amounts as K⁺. Release of K⁺ from the endosmotic cell half was stimulated remarkably by lowering the temperature from 20 to 1 °C, and also by lowering the internal osmotic pressure but inhibited by raising it.The dependence of K⁺ release on osmotic gradient, internal osmotic pressure and temperature can be explained by their effects on membrane depolarization and membrane resistance (Hayama et al. 1978). We concluded thatP _K remained unchanged, whileP _Cl increased a great deal in the endosmotic cell part.     

Growth of Pediococcus soyae nov. sp. in Highly Concentrated Solutions of Inorganic Salts and Sugars

Pediococcus soyae nov. sp., which has an inherited salt tolerant nature, is grown in solutions of high osmotic pressure. When this strain is transferred from 0.5% salted medium to a new medium containing 18% sodium chloride, the viable counts of this organism firstly decrease from about one half to one-third of the inoculated cells, and then normal growth occurs. This indicates the occurrence of physiological adaptation at an early stage of growth.

The growth of this lactic acid bacterium is observed in concentrated solutions of various inorganic salts. The solutions containing Na⁺, K⁺, Cl^?, NO₃^? and SO₄^{– –} ions are not toxic for the organism, and the organism can grow in solutions of 133 atm. osmotic pressure, generally. However, Li⁺, Ca⁺⁺, Mg⁺⁺ and Br⁺ are, toxic for growth.

In concentrated sugar solutions, this organism also propagates well, and growth is observed in the media containing 50% glucose or 60% sucrose, osmotic pressure being 105 and 84 atm., respectively. Therefore, Pediococcus soyae nov. sp. is osmotolerant.     

Effect of anisotonic media on cell volume and electrolyte fluxes in slices of the dogfish (Squalus acanthias) rectal gland

Summary Osmotic responses of slices of dogfish rectal gland to hypotonic (urea-free) and hypertonic media were studied. Transfer of tissue from isotonic (890 mosM) to hypotonic (550 mosM) saline produced an osmotic swelling associated with a slow net uptake of cell K⁺ (and Cl^–) and a slow, two-component efflux of urea. Media made hypertonic (1180 mosM) by addition of urea or mannitol produced osmotic shrinkage with a net loss of KCl. The cell osmotic responses in hypotonic media were lower than predicted for an ideal osmometer. No volume regulatory responses were seen subsequent to the initial osmotic effects. The cation influx in hypotonic media lacked specificity: in the presence of 0.5 mM ouabain or in K⁺-free media a net influx of Na⁺ was found. At steady state, the cell membrane potential evaluated from the Nernst potentials of K⁺ and triphenylmethyl phosphonium⁺, was independent of medium tonicity, suggesting the membrane potential as a determinant in the cellular osmotic response. Zero-time⁸⁶Rb⁺ fluxes were measured:⁸⁶Rb⁺ influx was not affected by hypotonicity, implying an unchanged operation of the Na⁺–K⁺-ATPase. On the other hand,⁸⁶Rb⁺ efflux was significantly reduced at hypotonicity; this effect was transient, the efflux returning to the control value once the new steady state of cell volume had been reached. A controlled efflux system is therefore involved in the cell osmotic response. The absence of the volume regulatory phenomenon suggests that the cells are not equipped with a volume-sensing mechanism.Abbreviations and symbols DW dry weight - E extracellular (polyethylene glycol) space - E Nernst potential - H₂O_e H₂O_i tissue water, extra- and intracellular - TPMP ⁺ triphenyl methyl phosphonium salt - WW wet weight