Assimilate transport in maize (Zea mays L.) seedlings at vertical low temperature gradients in the root zone

Even moderate chilling temperatures may cause important modifications in assimilate movement in maize seedlings from the shoot to the roots, but there is no information on long-distance transport of assimilates in plants subjected to vertical gradients of moderately low temperatures in the root zone. Seedlings of a chilling-tolerant (KW1074) and a chilling-sensitive inbred line (CM109) of maize were grown in a system that allowed the maintenance of temperature gradients between the topsoil (0-10 cm) and the subsoil (10-50 cm). After pregrowth at 24C until the third-leaf stage, plants were subjected to chilling-stress regimes for 6 d (17/17/17C, 17/17/12°C, 12/12/12°C, 12/12/17°C, air/topsoil/subsoil). The time taken for the assimilates to enter the phloem from the second leaf increased at low temperatures for both lines, but to a much greater extent in CM109. Although mainly influenced by air and topsoil temperature, low temperature in the subsoil also affected this trait in CM109. The speed of assimilate transport between the second leaf and the mesocotyl in KW1074 was strongly reduced by cool temperatures in the shoot and topsoil as well as by 12°C in the subsoil in CM109, because the latter line had a larger portion of its root system in the subsoil as compared to KW1074. The portion of assimilates allocated to the root decreased at low temperatures in both lines, but to a greater extent in CM109, and was controlled mostly by the subsoil temperature. After rewarming, values of all measured parameters of assimilate transport returned to near pregrowth levels within a few days.Keywords: Assimilate transport, low temperature stress, root growth, vertical soil temperature gradients, Zea mays L.      

Response of Douglas fir seedlings to phosphorus fertilization and influence of temperature on this response

Summary Effects of P fertilizers on growth of Douglas fir (Pseudotsuga menziesii var.menziesii (Mirb.) Franco.) seedlings were examined in pots and nursery beds. In pot experiments levels of P equivalent to 300 kg/ha were adequate for maximum growth over 14–18 weeks and resulted in available soil P levels of 80 ppm after 15 weeks' growth. Maximum growth in pots was obtained with shoot P concentrations of 0.18%–0.20%, with higher values at lower temperatures, but the optimum concentration for one-year old (1-0) nursery seedlings was 0.16% P. Growth of seedlings was greatly restricted at a soil temperature of 5°C and an air temperature of 12°C. At a soil temperature of 10°C and an air temperature of 14°C seedling P requirement was greater than at soil and air temperatures of 20°C.Comparison showed that monammonium phosphate was more effective than calcium superphosphate in stimulating growth in pots and nursery. Triple superphosphate was also effective in the nursery. Diammonium phosphate, potassium dihydrogen phosphate and phosphoric acid had no advantages as P sources in the nursery. Available P levels of 100–130 ppm, in the loamy sand and sandy loam nurseries studied, and needle P concentrations of 0.18%, when sampled in October, were associated with maximum growth of two-year old (2-0) seedlings.P fertilization decreased root/shoot ratio, but did not alter the allometric relationship of shoot to root. Improving P status from a low level increased root growth capacity in 2-0 seedlings and P fertilization of potted seedlings increased dry weight/height ratio. Uptakes per seed bed ha of 236 kg N, 31 kg P, 81 kg K and 73 kg Ca by 2-0 seedlings were comparable with, or greater than, uptake rates of agricultural crops. Recoveries of 6–11% of P from fertilizer were recorded in the nursery.     

Effect of a strong cold storage induced desiccation on metabolic solutes,stock quality and regrowth,in seedlings of two oak species

Bare-root seedlings of pedunculate oak (Quercus robur L.) and northern red oak (Quercus rubra L.) were lifted in January and stored at 1.8°C, at 82% relative humidity, until their fresh weight declined by 33%. Root growth potential (RGP), fine root electrolyte leakage (REL), fine root water content (RWC), shoot tip water content (SWC), starch and metabolic solute contents in root and shoot, were measured just after lifting and after treatment. Survival of treated seedlings was also assessed in a field trial. RWC, SWC, REL, RGP were dramatically affected by desiccation during cold storage. In both species, root soluble carbohydrate level, inositol level and isocitrate level increased, whereas root starch level and shoot soluble carbohydrate level decreased. In northern red oak, treated seedlings had higher root contents of soluble carbohydrates, inositol and proline than in pedunculate oak. Moreover, treatment induced proline accumulation only in northern red oak roots. These differences could explain why field survival of treated seedlings was significantly better in northern red oak than in pedunculate oak.     

The Effect of Root Temperature on Growth and Uptake of Ammonium and Nitrate by Brassica napus L. in Flowing Solution Culture: I. GROWTH

Macduff, J. H., Hopper, M. J. and Wild, A. 1987. The effectof root temperature on growth and uptake of ammonium and nitrateby Brassica napus L. in flowing solution culture. I. Growth.—J.exp. Bot. 38: 42–52 Oilseed rape (Brassica napus L. cv. Bien venu) was grown for49 d in flowing nutrient solution at pH 6?0 with root temperaturedecrementally reduced from 20?C to 5?C; and then exposed todifferent root temperatures (3, 5, 7, 9, 11, 13,17 or 25?C)held constant for 14 d. The air temperature was 20/15?C day/nightand nitrogen was supplied automatically to maintain 10 mmolm^–3 NH₄NO₃ in solution. Total dry matter production wasexponential with time and similar at all root temperatures givinga specific growth rate of 0?0784 g g^–1 d^–1. Partitioningof dry matter was influenced by root temperature; shoot: rootratios increased during treatment at 17?C and 25?C but decreasedafter 5 d at 3?C and 5?C. The ratio of shoot specific growthrate: root specific growth rate increased with the ratio ofwater soluble carbohydrates (shoot: root). Concentrations ofwater soluble carbohydrates in shoot and root were inverselyrelated to root temperature; at 3, 5 and 7?C they increasedin stem + petioles throughout treatment, coinciding with a decreasein the weight of tissue water per unit dry matter. These resultssuggest that the accumulation of soluble carbohydrates at lowtemperature is the result of metabolic imbalance and of osmoticadjustment to water stress. Key words: Brassica napus, oilseed rape, root temperature, specific growth rate     

Influence of root temperature on growth of Pinus sylvestris,Fagus sylvatica,Tilia cordata and Quercus robur

One-year-old tree seedlings were incubated in a greenhouse from April to July, under natural daylight conditions, with their root systems at constant temperatures of 5, 10, 15, 20, 25, 30 and 35 °C and with the above ground parts kept at a constant air temperature of 18–20 °C. The course of height growth, total mass increment, root, shoot and leaf weight as well as leaf areas were measured. The results indicate that clear differences exist in the optimal root zone temperatures for various growth parameters in different tree species. Pinus sylvestris had a maximal height increment at about 5–10 °C and maximal total mass increment at 15 °C root temperature. In contrast, the optimum for Quercus robur was at 25 °C. Tilia cordata and Fagus sylvatica had their optima for most growth parameters at 20 °C. The root temperature apparently indirectly influenced photosynthesis (dry weight accumulation) and respiration loss. From the observed symptoms and indications in the literature it seems probable that a change in hormone levels is involved as the main factor in the described effects. Variation of root temperature had only an insignificant effect on bud burst and the time at which the shoots sprouted. Apparently species of northern origin seem to have lower root temperature optima than those of more southern origin. This is to be verified by investigation of other tree species.     

Bud dormancy and vegetative growth in Salix polaris as affected by temperature and photoperiod

Summary Vegetative growth of two ecotypes (lat. 78° 15N and 69°37N) of Salix polaris L. was studied in phytotron experiments. Dormancy of the winter buds was broken by chilling at 0.5°C for 14 to 42 days. Chilling requirement increased with decreasing growth temperature. The optimum temperature for bud break and shoot growth was about 15°C for both ecotypes. Cessation of apical shoot growth and abscission of shoot tip was not prevented by long photoperiods. However, at high temperature, 15°C or more, and in 18 to 24 h photoperiod, two or three growth flushes occurred frequently in both ecotypes. Leaf abscission in the arctic ecotype from lat. 78°N was not affected by photoperiod when grown at 6°C, but was stimulated by short photoperiod when grown at 15°C. In the ecotype from lat. 69°N leaf abscission was enhanced by short photoperiod even at 6°C.     

An assessment of the role of ethylene in mediating lettuce (Lactuca sativa) root growth at high temperatures

Growth of temperate lettuce (Lactuca sativa) plants aeroponically in tropical greenhouses under ambient root-zone temperatures (A-RZTs) exposes roots to temperatures of up to 40 degrees C during the middle of the day, and severely limits root and shoot growth. The role of ethylene in inhibiting growth was investigated with just-germinated (24-h-old) seedlings in vitro, and 10-d-old plants grown aeroponically. Compared with seedlings maintained at 20 degrees C, root elongation in vitro was inhibited by 39% and root diameter increased by 25% under a temperature regime (38 degrees C/24 degrees C for 7 h/17 h) that simulated A-RZT in the greenhouse. The effects on root elongation were partially alleviated by supplying the ethylene biosynthesis inhibitors aminooxyacetic acid (100-500 microM) or aminoisobutyric acid (5-100 microM) to the seedlings. Application of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid to seedlings grown at 20 degrees C mimicked the high temperature effects on root elongation (1 microM) and root diameter (1 mM). Compared with plants grown at a constant 20 degrees C root-zone temperature, A-RZT plants showed decreased stomatal conductance, leaf relative water content, photosynthetic CO(2) assimilation, shoot and root biomass, total root length, the number of root tips, and root surface area, but increased average root diameter. Addition of 10 microM ACC to the nutrient solution of plants grown at a constant 20 degrees C root-zone temperature mimicked the effects of A-RZT on these parameters but did not influence relative water content. Addition of 30 microM aminoisobutyric acid or 100 microM aminooxyacetic acid to the nutrient solution of A-RZT plants increased stomatal conductance and relative water content and decreased average root diameter, but had no effect on other root parameters or root and shoot biomass or photosynthetic CO(2) assimilation. Although ethylene is important in regulating root morphology and elongation at A-RZT, the failure of ethylene biosynthesis inhibitors to influence shoot carbon gain limits their use in ameliorating the growth inhibition induced by A-RZT.     

Temperature changes and the geotropic reaction of the radicle of zea mays L.

Summary The relationship between the geotropic reaction of the maize radicle and changing temperatures was investigated with seedlings grown in soil, in vermiculite, and between sheets of chromatographic paper. The seeds were oriented horizontally and vertically and the angle to vertical of several successive 2-cm segments of each radicle was measured.Constant temperatures of 17°C and 33°C and cyclic temperatures with times of 1, 3, 6, 12 and 18 hours at 33°C, the remaining time of the 24 hour cycle at 17°C were imposed on maize seedlings. The most horizontal radicles occurred at constant 17°C (0 hours at 33°C) and the most vertical radicles occurred in cycles with 1 and 3 hours at 33°C. Longer times at 33°C up to and including constant 33°C produced increasingly more horizontal radicles. Curvature of the radicles in response to temperature continued with distance from the seed.Slightly more horizontal growth occurred with radicles from seeds oriented horizontally rather than vertically. However, radicles from both seed orientations responded similarly to temperature and distance from the seed.These observations were noted with growth in two and three dimensions and from experiments in several different growth chambers. A further experiment indicated that a change toward more vertical growth could be induced with a single change in temperature from 17°C to 33°C. re]19760413     

Comparison of the effects of nitrate and ammonium forms of nitrogen on auxin content in roots and the growth of plants under different temperature conditions

Average root length, root/shoot ratio and auxin content in roots were higher in plants supplied with nitrate rather than ammonium and grown at 18, 21, 24°C. The effects on root length were most pronounced at the highest temperatures (21 and 24°C); and the warmer the temperature, the earlier appearance of the differences in growth rate between NO₃- and NH₄-fed plants. A sharp acceleration of root growth was characteristic of NO₃-fed plants grown at 21 and 24°C and was associated with a temporary increase in auxin concentration measured by immunoassay.     

Effect of soil temperature on nutrient allocation and mycorrhizas in Scots pine seedlings

We studied the effect of soil temperature on nutrient allocation and mycorrhizal development in seedlings of Scots pine (Pinus sylvestris L.) during the first 9 weeks of the growing season. One-year-old seedlings were grown in Carex-peat from a drained and forested peatland at soil temperatures of 5, 9, 13 and 17 °C under controlled environmental conditions. Fourteen seedlings from each temperature treatment were harvested at intervals of three weeks and the current and previous year's parts of the roots, stems and needles were separated. Mineral nutrient and Al contents in all plant parts were determined and the tips and mycorrhizas of the new roots were counted. Microbial biomass C and N in the growth medium were determined at the end of the experiment. None of the elements studied, except Fe, were taken up from the soil by the seedlings during the first three weeks. Thereafter, the contents of all the elements increased at all soil temperatures except 5 °C. Element concentrations in needles, stems and roots increased with soil temperature. Higher soil temperature greatly increased the number of root tips and mycorrhizas, and the numbers of mycorrhizas increased more than did the length of new roots. Cenococcum geophilum was relatively more abundant at lower soil temperatures (5 and 9 °C) than at higher ones (13 and 17 °C). A trend was observed for decreased microbial biomass C and N in the peat soil at higher soil temperatures at the end of the experiment.     

Effects of soil temperature on root and shoot growth traits and iron deficiency chlorosis in sorghum genotypes grown on a low iron calcareous soil

Iron deficiency chlorosis (FeDC) is a common disorder for sorghum [Sorghum bicolor (L.) Moench] grown on alkaline calcareous soils. Four sorghum genotypes were grown in growth chambers on a low Fe (1.3 g/g DTPA-extractable), alkaline (pH 8.0), calcareous (3.87% CaCO₃ equivalent) Aridic Haplustoll to determine effects of different soil temperatures (12, 17, 22 and 27°C at a constant 27°C air temperature) on various root and shoot growth traits and development of FeDC. As soil temperature increased, leaf chlorosis became more severe, and shoot and root dry weights, root lengths, and leaf areas increased markedly. Shoot/root ratios, shoot weight/root length, leaf area/shoot weight and leaf area/root weight and root length also increased while root length/root weight decreased as soil temperature increased. Severe FeDC developed in all genotypes even though genotypes had previously shown different degrees of resistance to FeDC. Genotypes differed in most growth traits, especially dry matter yields, root lengths, and leaf areas, but most traits did not appear to be related to genotype resistance to FeDC. The most FeDC resistant genotype had the slowest growth rate and this may be a mechanism for its greater resistance to FeDC.     

The effect of rhizosphere dissolved inorganic carbon on gas exchange characteristics and growth rates of tomato seedlings

The possibility that an enhanced supply of dissolved inorganic carbon (DIC=CO2+HCO3^-) to the root solution could increase the growth of Lycopersicon esculentum (L.) Mill. cv. F144 was investigated under both saline and non-saline root medium conditions. Tomato seedlings were grown in hydroponic culture with and without NaCl and the root solution was aerated with CO2 concentrations in the range between 0 and 5000 mol mol^-1. The biomass of both control and salinity-stressed plants grown at high temperatures (daily maximum of 37C) and an irradiance of 1500 mol m^-2 s^-1 was increased by up to 200% by enriched rhizosphere DIC. The growth rates of plants grown with irradiances of less than 100 mol m^-2 s^-1 were increased by elevated rhizosphere DIC concentrations only when grown at high shoot temperatures (35C) or with salinity 28°C). At high light intensities, the photosynthetic rate, the CO2 and light-saturated photosynthetic rate (jmax) and the stomatal conductance of plants grown at high light intensity were lower in plants supplied with enriched compared to ambient DIC. This was interpreted as 'down-regulation' of the photosynthetic system in plants supplied with elevated DIC. Labelled organic carbon in the xylem sap derived from root DI¹⁴C incorporation was found to be sufficient to deliver carbon to the shoot at rates equivalent to 1% and 10% of the photosynthetic rate of the plants supplied with ambient- and enriched-DIC, respectively. It was concluded that organic carbon derived from DIC incorporation and translocated in the xylem from the root to the shoot may provide a source of carbon for the shoots, especially under conditions where low stomatal conductance may be advantageous, such as salinity stress, high shoot temperatures and high light intensities.     

Developmental Physiology of Sugar-beet: IV. EFFECTS OF GROWTH SUBSTANCES AND DIFFERENTIAL ROOT AND SHOOT TEMPERATURES ON SUBSEQUENT GROWTH

The effects of three growth substances, viz. indol-3yl-aceticacid (IAA), gibberellic acid (GA₃), and kinetin (KIN), and differentialshoot and root temperatures on growth of sugar-beet (Beta vulgarisL.) plants have been studied. IAA, GA₃, and KIN were applied in aqueous lanolin at differentconcentrations (50 ppm to 5000 ppm) to decapitated sugar-beetplants at the eight-leaf stage, one group also having alternateleaves removed. The growth substances significantly increasedthe dry weights of the plants when all the leaves were present,which was mainly explained by the large increase in roots. Thegrowth substances probably stimulated cambial activity and hencethe mobilization of substrates resulting in a bigger root whena relatively large leaf area existed. The failure of the plantsto respond to treatments following the removal of alternateleaves suggests that under such conditions the growth substanceshave hardly any major effect on the production of substrates;rather they influence growth by regulating the movement of substratesby altering the ‘sink strength’ if the supply ofsubstrates is not limiting. It could also be that the rootsproduce sufficient growth substances to maintain half the leavesat maximum expansion and maximum photosynthesis. Treatment withgrowth substances would therefore have little effect. When allthe leaves were present, they are limited by insufficient growthsubstances. All combinations of root and shoot temperatures of 17 and 25°C were imposed on plants decapitated at the eight-leafstage, one group also having each alternate leaf removed. Leaf8 expanded most at shoot and root temperature of 25 °C whereasother leaves had the largest areas at shoot and root temperatureof 17 °. When all the leaves were present root growth wasmaximal at shoot temperature of 17°C and root temperatureof 25 °C, but when alternate leaves were removed maximumroot growth occurred at shoot and root temperatures of 25 °C.Generally, a higher concentration of soluble carbohydrates wasfound in the roots and leaves when either the shoot or rootor both were kept at 17 °C. Concentrations of nitrogen,phosphorus, and potassium in different organs were less at 17°C than at higher shoot or root temperatures and decreasedwith age.     

Effect of planting date,ventilation and soil temperature on growth and nutrition of tomato in high tunnels

Growth rates and tissue nutrient concentrations were measured in tomato (Lycopersicon esculentum Mill) grown in unheated high tunnels in the spring in the northeast USA. Two weeks after transplant on 3 April, seedlings had low concentrations of Nitrogen, Magnesium and other nutrients, while later plantings on 17 April and 1 May had adequate nutrition. The low yield and small fruit of the 3 April planting, compared to the later plantings, was likely related to this nutrient stress soon after transplant. Air and soil temperatures were less than 10°C at planting on 3 April. Air and soil were warmed during the day to different extents in tunnels vented at different temperatures. Over all plantings and ventilation regimes, relative growth rates over the two weeks after transplant were correlated to average air temperature. However, there was little uptake of P, N and Mg, when soil was cooler than 12°C. Nutrient concentrations in the shoot became very low because shoot growth continued when soil temperature limited nutrient uptake.     

Soil temperature and flooding effects on two species of citrus

Summary Rough lemon (Citrus jambhiri Lush.) and sour orange (C. aurantium L.) seedlings were grown at constant soil temperatures of 16, 24, and 33 C for 3 months. Shoot and root growth of rough lemon was greatest at 33 C while growth of sour orange was greatest at 24 C. There were no significant effects of soil temperature on shoot: root ratio, leaf water potential or stomatal conductance. The hydraulic conductivity of intact root systems of both species was highest when seedlings were grown at 16 C. Thus, acclimation through greater root conductivity at low soil temperature may have compensated for decreased root growth at 16 C and negated effects of soil temperature on plant water relations. Half the plants growing at each soil temperature were subsequently flooded. Within 1 week, the soil redox potential (Eh) dropped below zero mV, reaching a minimum Eh of –250mV after 3 weeks of flooded conditions. Flooded plants exhibited lower root conductivity, a cessation of shoot growth, lower leaf water potentials, lower stomatal conductances, and visual sloughing of fibrous roots. Decreases in root conductivity in response to flooding were large enough to account for the observed decreases in stomatal conductance.Florida Agricultural Experiment Stations Journal Series No. 4080.     

Effect of sub-optimal root zone temperatures at varied nutrient supply and shoot meristem temperature on growth and nutrient concentrations in maize seedlings (Zea mays L.)

Maize seedlings were grown for 10 to 20 days in either nutrient solution or in soils with or without fertilizer supply. Air temperature was kept uniform for all treatments, while root zone temperature (RZT) was varied between 12 and 24°C. In some treatments the basal part of the shoot (with apical shoot meristem and zone of leaf elongation) was lifted up to separate the indirect effects of root zone temperature on shoot growth from the direct effects of temperature on the shoot meristem.Shoot and root growth were decreased by low RZT to a similar extent irrespective of the growth medium (i.e. nutrient solution, fertilized or unfertilized soil). In all culture media Ca concentration was similar or even higher in plants grown at 12 as compared to 24°. At lower RZT concentrations of N, P and K in the shoot dry matter decreased in unfertilized soil, whereas in nutrient solution and fertilized soil only the K concentration decreased.When direct temperature effects on the shoot meristem were reduced by lifting the basal part of the shoot above the temperature-controlled root zone, shoot growth at low RZT was significantly increased in nutrient solution and fertilized soil, but not in unfertilized soil. In fertilized soil and nutrient solution at low RZT the uptake of K increased to a similar extent as plant growth, and thus shoot K concentration was not reduced by increasing shoot growth rates. In contrast, uptake of N and P was not increased, resulting in significantly decreased shoot concentrations.It is concluded that shoot growth at suboptimal RZT was limited both by a direct temperature effect on shoot activity and by a reduced nutrient supply through the roots. Nutrient concentrations in the shoot tissue at low RZT were not only influenced by availability in the substrate and dilution by growth, but also by the internal demand for growth.     

Root-zone temperature effects on the early development of maize

Summary Maize plants were grown in sand culture under greenhouse conditions from emergence to the 4-leaf stage at root-zone temperature of 12.5°, 15° and 17.5°C in one experiment, and grown to the 6-leaf stage at root zone temperatures of 15°, 20°, and 25°C in a second experiment. Attention was given to plant part differentiation as determined by leaf appearance, and to growth as determined by dry tissue accumulation, at specified growth stages.For anyone growth-stage interval the number of days required for that interval increased with decreasing root-zone temperature. Dry weights of both roots and shoots at the various growth stages decreased with increasing root-zone temperature. Root zone temperature had a direct influence on the meristematic region of the shoots of young maize plants because of the close proximity of this region to the ground surface and thereby regulated plant development during the period of leaf initiation.Increased root-zone temperature enhanced plant development rate relative to plant growth rate thus reducing the ultimate yield of maize at the 4- and 6- leaf stages.It was concluded that because of the direct influence of root-zone temperature on the shoot meristem and hence on the nutrient demands of the shoot, due consideration should be given to this factor in studies concerned with soil temperature.Agronomy Department Paper No. 709.     

Rapid acclimation of root hydraulic conductivity to low temperature

Root hydraulic conductance of many species is substantially reduced by exposure to low temperatures. The objective of this research was to investigate the decrease and recovery of root hydraulic conductivity in spinach (Spinacia oleracea L.) root systems upon exposure to low temperature. Root hydraulic conductivity (Lp) was determined for detached whole root systems as the slope of the flux and an applied pressure gradient. Water flux (Jv), of root systems grown at 20C, decreased immediately upon exposure to 5C. After 2-5 h Jv recovered and reached a stable value after 12 h exposure to 5°C. In separate experiments, the root Lp of plants acclimated for 7 d at 5°C was 125% greater than that of isolated root systems acclimated for 12 h at 5°C. Lp of plants grown and measured at 5°C was about 50% of the Lp of plants grown and measured at 20°C. The rapid acclimation to low temperatures observed in detopped root systems was also indicated in intact plants at 20/5°C (shoot/root temperatures) using mass flow porometry. Acclimation of the root system after exposure to 5°C was apparent by recovery of stomatal opening. These results indicate that spinach root systems have the ability to acclimate rapidly to changes in temperature and to continue acclimating during prolonged exposure to low temperature.     

Evaluation of host and pathogen responses for screening soil amendments to control Sclerotium rolfsii

Three strains of Bradyrhizobium, 280A, 2209A and 32H1, that nodulated peanuts (Arachis hypogaea L.), were tested for their ability to grow and survive at elevated temperatures of up to 42°C in laboratory culture. Strain 32H1 was unable to grow at 37°C and was more sensitive to elevated temperatures than the other two strains. All three produced heat-shock proteins of molecular weights 17 kDa and 18 kDa. Two greenhouse experiments were conducted to determine the effect of high root temperature on nodulation, growth and nitrogen fixation of peanut. Two peanut varieties (Virginia cv NC7 and Spanish cv Pronto) were inoculated and exposed to root temperatures of 30°, 37° and 40°C. Nodulation and nitrogen fixation were strongly affected by root temperature but there was no variety × temperature interaction. At a constant 40°C root temperature no nodules were formed. Nodules were formed when roots were exposed to this temperature with diurnal cycling but no nitrogen fixation occurred. Highest plant dry weight, shoot nitrogen content and total nitrogen were observed at a constant root temperature of 30°C. Increasing root temperature to 37°C reduced average nitrogen content by 37% and total nitrogen by 49% but did not reduce nodulation. The symbiotic performance of the strains corresponded to their abilities to grow and survive at high temperature in culture.     

Fatty acid composition of microsomal phospholipids and H+-ATPase activity in the roots of Scots pine seedlings grown at different root temperatures during flushing

The fatty acid composition of phospholipids in the microsomesand the vanadate-sensitive H⁺-ATPase activity of the roots ofone-year-old Scots pine (Pinus sylvestris L.) seedlings werestudied during flushing in spring. The seedlings in hydroponiccultures were subjected to different root temperatures (5, 12or 20°C). The shoot was maintained at 20/15° C (day/night)during the 35 d experiment. After 35 d at 5° C, root growthwas totally inhibited and shoot growth partly inhibited. In roots grown at 5° C the fatty acid composition of themicrosomal phospholipids and the degree of fatty acid unsaturation(bond index) were unchanged, while in roots grown at 12 and20° C the fatty acid composition changed and bond indexdecreased. At those root temperatures, the most obvious changewas a decline in the proportion of linolenic acid (C18:3). Inthe new white roots grown either at 12°C or 20°C theproportion of C18:2 was higher and the proportion of C18:3 lowerthan in 1-year-old roots. Independently of root temperature,H⁺-ATPase activity, determined on a fresh weight basis, declinedto half of the original activity during the experiment. Thedecline in H⁺ -ATPase activity was most rapid during the firstweek. In the old roots the decline in H⁺-ATPase activity followedclosely the decline in amount of membrane protein. In new rootsH⁺-ATPase activity was high and increased with increasing roottemperature. These results suggest that in the roots of Scotspine seedlings, vanadate-sensitive H⁺-ATPase activity is dependenton age, while changes in the microsomal fatty acid compositionof phospholipids are regulated mainly by root temperature. Key words: Fatty acids of phospholipids, microsomes, H⁺-ATPase, root temperature, Scots pine