The Influence of Temperature on Seed Germination Rate in Grain Legumes: I. A COMPARISON OF CHICKPEA, LENTIL, SOYABEAN AND COWPEA AT CONSTANT TEMPERATURES

For a single seed population of each of four species of grainlegume positive linear relationships were shown between temperatureand rate of germination for different fractions (G) of eachpopulation, from a base temperature, T_b(G), at which germinationrate is zero, to an optimum temperature, T_o(G) at which germinationrate is maximal. At constant temperatures warmer than T_o(G)there were negative relations (probably linear) between temperatureand rate of germination to the maximum temperature for germination,T_m(G), Within each population T_b(G) did not differ, but it didvary between species, viz.0.0?C, 0.25?C, 4.and 8.5?C for chickpea(Cicer arietinum L.), lentil (Lens culinaris Medic.), soyabean(Glycine max [ Merr.) and cowpea (Vigna unguiculata [L.] Walp.),respectively. In contrast, T_o(G) varied both within each populationand also between the four species: 80% of seeds in each populationhad T_o(G) values within the range 31.8?C to 33.8 ?C, 24.0?Cto 24.4?C, 34.0?C to 34.5?C and 33.2?C to >40?C, respectively.Values of T_m(G) were much more vanable: the 80% population rangewas 48 .0?C to 60.8?C for chickpea, 31.8?C to 34.4?C for lentiland 46.8?C to 55.2?C for soyabean; reliable estimates couldnot be made for cowpea, but the results suggest higher and morevariable values of T_m(G) than in the other three species. Atsub-optimal temperatures the distribution of thermal time forthe different fractions of each population was normal, exceptfor lentil where it was log-normal. A single equation is proposedto describe the influence of sub-optimal temperatures on ratesof germination for whole seed populations. At supra-optimaltemperatures, variation in thermal time for the different fractionsof each population was only slight. The implications of thesefindings for the adaptation of grain legume crops to differentenvironments, and for the screening of germplasm, are discussed. Key words: Seed germination rate, temperature, grain legumes     

Antitranspirant-induced Heat Stress in the Parasitic Plant Striga hermonthica--A Novel Method of Control

Leaf temperatures (T₁) of the parasitic plant Striga hermonthicaare substantially below those of the air (T_a), [T_a–T₁]reaching 7 ?C at T_a = 40 ?C. This results from high rates oftranspiration and the consequent evaporative cooling of theleaf. Application of an antitranspirant, which mechanicallyimpedes foliar loss of water vapour, reduced transpiration andstomatal conductance by 40% and 57%, respectively, and reduced[T_a– T₁] to 2 ?C at T_a = 40 ?C. The temperature sensitivityof photosynthesis in the host-parasite association differed,the optima (T_opt) being 37.2 and 40.1 ?C for S. hermonthicaand sorghum, respectively. Once Topt had been exceeded in S.hermonthica net photosynthesis declined rapidly, reaching thelethal limit (Tmax) at 42.6 ?C. S. hermonthica is particularlysensitive to high temperatures and antitranspirant-induced overheatingleads to blackening and shrivelling of the leaf after as littleas 4 h at T_a = 40 ?C. Application of an antitranspirant underfield conditions in the Sudan at T_a = 40 ?C resulted in 28%and 67% reductions in transpiration and stomatal conductance,together with a 5 ?C increase in T₁, and subsequent leaf death.In addition to these short-term physiological responses, antitranspirantspraying of the arasite increased the grain and straw yieldof the crop by factors of 3.4 and 2.6, respectively. Antitranspirantsmay have potential use as a method of controlling Striga inthe field. Key words: Striga hermonthica, sorghum, photosynthesis, transpiration, high temperature stress, anti-transpirant     

Effect of Root Temperature on the Infection Processes and Nodulation in Lotus and Stylosanthes

Infection threads were observed abundantly in the root hairsof Lotus corniculatus L., but very rarely in L. hispidus, Desf.,in response to infection by Rhizobium strains 3001 and 3002.Numbers of infections differed between species and strains andwere also affected by temperature. In L. corniculatus all thenodules originated from infection threads, but in L. hispidusmost nodules appeared to originate by direct bacterial penetrationthrough the epidermis, and infected root hairs were very rarelyseen. Both species of Lotus were tolerant to cold temperatures,the minimum temperature for nodulation being 10 ?C. The optimumtemperature for nodulation of L. corniculatus was 20 ?C with3001 and between 27 and 30 ?C with 3002, a few nodules beingformed with both strains at 35 ?C. L. hispidus formed more nodulesthan L. corniculatus and the optimum temperature for both thestrains was between 25 and 27 ?C. No infection threads were seen in root hairs or nodules of Stylosanthesguyanensis (Aubl.) S. W. and S. humilis H.B.K. infected withRhizobium strain CB1552, and all the nodules were formed inthe axils of lateral roots. Optimum temperature for nodulationin S. guyanensis and S. humilis was around 27 ?C; nodulationwas completely inhibited at 15 ?C and very few nodules wereformed at 35 ?C. Both in Lotus and Stylosanthes the transfer of plants from suboptimalto optimal and supraoptimal temperatures increased nodulation.Delayed inoculation and excision of root tips increased nodulation.     

Initiation of Rapid Ethylene Synthesis by Apple and Pear Fruits in Relation to Storage Temperature

The influence of storage temperature on the onset of rapid ethyleneproduction was investigated for fruits of Conference pear (Pyruscommunis L.) and five cultivars of apple (Malus domestica Borkh.).The time taken from harvest to rapid ethylene production wasshorter and more uniform at 3 ?C than at 18–20 ?C forConference pears and Golden Delicious apples. Increases in internalethylene concentration, 1-amino cyclopropane-1-carboxylic acidconcentration and ethylene production were simultaneous in GoldenDelicious apples at 3 ?C. When Golden Delicious apples wereheld at 3 ?C for 48 h and then kept at 20 ?C the mean time ofonset of ethylene production was similar to that for applesheld continuously at 20 ?C. However, two periods of 48 h at3 ?C caused earlier ethylene production. Conversely, ethyleneproduction at 3 ?C was delayed by transfer to 20 ?C for twoperiods of 48 h. Cox's Orange Pippin and other apple cultivarstended to show more synchronous ethylene production at 3 ?Cthan at higher temperatures but the mean time of onset was eitherunaffected by temperature or slighdy delayed at lower temperature.Acceleration of the onset of ethylene production by low temperaturewas never observed in Cox's Orange Pippin apples harvested atweekly intervals from 10 August to 17 September. Key words: Ethylene, Storage temperature, Pyrus communis, Malus domestica     

Effects of temperature on the cytokinin requirement of tobacco calluses

A cytokinin-nonrequiring strain (T22) was isolated from a cytokinin-requiringcallus strain T2 of tobacco (Nicotiana tabacum var. Bright Yellow). Strain T22 grew rapidly on the medium without added kinetinat 26?C. But its growth was completely suppressed at 16?C. Thisgrowth suppression at 16?C was partially recoverable by supplyingkinetin. Benzyladenine, geranylaminopurine and 2-methyl-8-benzylamino-s-triazolo[l,5-a]pyrazinewere also effective in removing growth suppression at 16?C.Adenine, which was unable to remove growth suppression of T22at 16?C, promoted the growth of T2 at 26?C, but not at 16?C.Physiological differences between cytokinin-requiring and -nonrequiringcalluses are discussed. ¹Part II in the series "Studies, on Plant Tissue Cultures";for Part I, See Plant & Cell Physiol. 9: 103–114 (1968). (Received May 29, 1970; )     

Alterations in the Heat Response of Chlorella ellipsoidea by Deuteration

For the elucidation of the isotope effect on cell functionsof deuterium (D) incorporated into cell constituents, alterationsin the heat response of D-exchanged Chlorella ellipsoidea (D-Chlorella)were investigated. D-Chlorella cells obtained by culture inmedium that contained 60 mol% D₂O were assayed for their responseto heat in H₂O medium to rule out the solvent isotope effectof D₂O. Upon heating at 41–45?C, the heat sensitivityof D-Chlorella was greater than that of ordinary (H-Chlorella)cells; at 43?C, the heat sensitivity of D-Chlorella was 1.5–1.6times higher than that of H-Chlorella. For the induction ofresistance to heating, preheating of the cells at a lower temperaturethan that used for heat treatment was effective in the caseof both D- and H-Chlorella. However, the optimum temperaturefor preheating of D-Chlorella (34?C) was lower than for H-Chlorella(36–37?C). With preheating at 34?C, heat-shock proteins(HSPs), in particular proteins of 62 and 79 kDa, were inducedsimilarly in both types of cell. However, the gel-electrophoreticpatterns of HSPs induced at 37?C were differed somewhat betweenD- and H-Chlorella. These results suggest that the responseof cells to heat, in particular the induction of resistanceto heating and the synthesis of HSPs, was altered by deuterationof cell constituents. (Received June 11, 1990; Accepted November 24, 1990)     

Effects of temperature and light on the population dynamics of the Asterionella-Rhizophydium association

Growth parameters of the diatom Astenonella formosa Hass, andits fungal parasite Rhizophydium planktoniacum Canter emend,were measured at five temperatures and six light intensitieswith a 15?9 h light:dark cycle, using laboratory cultures ofboth organisms. With the parameter values obtained, thresholdhost densities were calculated in order to estimate the effectsof light and temperature on survival and epidemic developmentof the parasite The uninfected host reached light-saturatedgrowth rates between 0.917 day^–1 at 21?C and 0 285 day¹at 2?C. Under light limitation the optimum growth temperaturefor Asterionella decreased because of a reduced growth efficiencyGrowth inhibition at high irradiances was only observed at 2?CThe parasite reached the highest zoospore production at 2?Cand saturating irradiances: 30 2 zoospores per sporangium. Thisvalue was consistently reduced by lower irradiances and highertemperatures to only 2.2 zoospores at the opposite light andtemperature extremes Low light conditions depressed also theinfectivity of the zoospores At very low irradiances, they becamecompletely uninfective The light dependence of zoospore productionand infectivity was restricted to light intensities that limitedthe growth rate of the host. The development time of the sporangiaand the mfecti ve lifetime of the zoospores were not affectedby light but only by temperature, and ranged from 19.0 and 121 days respectively at 2?C to 1.9 and 2 1 days at 21?C- Theseeffects result in optimal conditions for the development ofa Rhizophydium epidemic at 11?C and a moderate light limitationof Astenonella At temperature above 7?C, the possibilities forepidemic development are only slightly affected by light andtemperature, except for very low irradiance levels, when thezoospores of the parasite become uninfective. However, below5?C the development of an epidemic is only possible at limitinglight levels. Conditions for survival of the parasite at lowhost densities are optimal at low temperatures and high irradiancelevels     

Differences in cold lability of pyruvate, Pi dikinase among C4 species

The cold lability of pyruvate, Pi dikinase in crude leaf extractswas studied in a number of C⁴ plants. The survey included C⁴monocots and dicots and species representingthe three C⁴ subgroups:NADP-malic enzyme, NAD-malic enzyme, and PEP-carboxykinase types. In some species (e.g., Digitaria sanguinalis, Sorghum bicolorand Echinochloa crus-galli), the enzyme was very sensitive tocold treatment (half life of about 8 min at 0?C and 10 to 15min at 10?C). In other species (Panicum miliaceum, Panicum maximumand Panicum texanum), the enzyme was very cold tolerant (retentionof 60 to 85% activity after 60 min at 0?C and 90% activity after60 min at 10?C). Among the plants examined, the most cold sensitivepyruvate,Pi dikinase was found among species of the NADP-malicenzyme subgroup. (Received March 9, 1979; )     

Solute Leakage from Solanum nigrum L. Seeds Exposed to High Temperatures during Imbibition

Exposure of Solanum nigrum L. seeds to high temperatures duringimbibition affected their leakage pattern: (1) The rate of leakageof total electrolytes was markedly increased with elevationof temperature. The increase was highest during the first 3h of imbibition but with a reduced rate thereafter. (2) Leakageof Na⁺ was almost complete after 6 h of imbibition at both temperatures,but much more Na⁺ leaked out at 50?C than at 25?C. (3) A markedincrease in leakage of K⁺ occurred after 24 h of exposure to50?C so that after 96 h three times more K⁺ leaked out at 50?Cthan at 25?C. (4) After 6 h of imbibition Ca11 and Mg⁺⁺ continuedto leak out at 25?C and at 50?C at a similar rate. (5) Imbibitionat an elevated temperature induced a marked increase in theleakage of both nucleic acids and proteins. (6) Malate dehydrogenasewas not detected in the leachate at 25?C, but was found after48 h at 50?C. It is assumed that this enzyme was of cytoplasmicorigin, indicating heat damage to membranes. The possible roleof the above phenomena in the loss of viability of the seedsdue to exposure to high temperature during imbibition is discussed. Key words: Leakage, Germination, S. nigrum     

Quantal Response of Fruit and Seed Germination Rate in Quercus robur L. and Castanea sativa Mill, to Constant Temperatures and Photon Dose

A linear relationship between constant temperatures in the sub-optimaltemperature range and germination rate is shown in both Quercusrobur L and Castanea sativa Mill germinated under nominal darkconditions. The mean base temperature was interpolated for Qrobur as 0 8 ? or 2-4 ?, depending on seed lot provenance, andfor C. sativa as 1 -4? The optimum temperature for germinationin Q. robur was about 20? compared with around 28 ? in C. sativaOver the sub-optimal temperature range the distribution of thermaltimes was log-normal for each population studied their spreadvarying both between Q robur seed lots and between species However,in C. sativa germinated close to the mean base temperature,the distribution in thermal times was reduced Thermal timesto germination were decreased in Q. robur and C sativa by approximately0 3 and 0-5 log-units, respectively, when the pericarp was removed,i.e in the seeds, but the sensitivity of the response remainedrelatively unaltered In both species the germination rate was the same when nominaldark or safe green light conditions were employed during thegermination test. However, at 21 ? Q robur exhibited the highirradiance reaction (HIR) at photon doses above 30mmol m^–2d^–1. HIR first affected the germination rate by an inhibitionof radicle extension The sensitivity of the response to thermaltime was reduced as photon dose increased. This photo-inhibitionwas exacerbated at supra-optimal temperatures. In contrast,C. sativa germination rate at 26 ? was little influenced bylight at a photon dose of 752 mmol m^–2 d^–1 Key words: Seed germination rate, temperature, thermal time, light, photon dose     

A Cold-Sensitive spo14 Mutation Affecting Ascospore Formation in the Fission Yeast Schizosaccharomyces pombe

In the fission yeast Schizosaccharomyces pombe, twenty sporulation-specificgenes (spo1–spo20) have been identified and analyzed.We found that a mutation designated spo14–221 caused cold-sensitivesporulation: ascospores were formed at 30?C but not at 23?C.Nuclear staining with 4',6-diamidino-2-phenylindole revealedthat a strain with this mutation completed meiosis even at therestrictive temperature. Electron microscopy showed that assemblyof forespore membranes during meiosis II was abnormal and incompletein the mutant cultured at 23?C. Temperature-shift experimentsindicated that the cold-sensitive period began during earlymeiosis I and terminated with the end of meiosis II. These resultssuggest that the product of the spo14 gene is synthesized andexecutes its function prior to the expression of the sporulation-deficientphenotype of the mutant, prior to the formation of the abnormalforespore membrane. (Received October 5, 1989; Accepted February 28, 1990)     

Use of the Weibull Function to Calculate Cardinal Temperatures in Faba Bean

The onset of germination of faba bean seeds at constant temperaturewas progressively delayed as that temperature diverged froman optimum of 25.5 ?C. At temperatures below 10 ?C, or above28 ?C, the maximum germination percentage fell to below 90%.There was no germination at 39 ?C. Positive and negative linearrelationships were established between the constant temperaturesand the rates of progress of germination to different percentiles,at sub-optimal and supra-optimal temperatures, respectively.Like germination rates, base temperature (T_b) declined from3.71 to –0.83 ?C as the percentile value increased from10% to 80%. Caution was urged in extrapolating beyond the experimentaldata set. Differences in the ceiling temperature (T_c) with percentilecould not be discerned. Cumulative germination progress curves at each temperature weremodelled by the Weibull, logistic, and cumulative normal distributionfunctions. Cardinal temperatures (T_b and T_c) calculated fromthese data reasonably approximated the actual data. The Weibullfunction demonstrated a good approximation at all percentilelevels, while the logistic and cumulative normal distributionfunctions, as a result of their inherent symmetry, deviatedat the extreme percentiles. It was concluded that the Weibullfunction not only accurately modelled cumulative germinationbut could also be used in the calculation of cardinal temperatures. Key words: Seed germination rate, cardinal temperatures, faba bean, Weibull function, probit and logic scales     

A Cryomicroscopic Study of Cylindrocystis brebissonii De Bary and Two Species of Micrasterias Ralfs (Conjugatophyceae, Chiorophyta) during Freezing and Thawing

The changes in morphology of the unicellular algae Cylindrocystisbrebissonii and two species of Micrasterias during freezingand thawing were observed on a light microscope fitted witha temperature controlled stage. At slow rates of cooling extensiveshrinkage of the protoplast was observed. The response of thecell wall varied with cell-type. In C. brebissonii plasmolysiswas not observed and the cell wall and protoplast shrank together.In Micrasterias the cell wall did not contract and a distinctplasmolysis was observed. Following freezing to and thawingfrom –25?C cells of C. brebissonii were non-viable butremained osmotically responsive. Cooling at faster rates inducedintracellular ice formation in all cell-types. The criticalrate of cooling varied with cell-type and was determined bycell volume and suface area. Intracellular gas bubbles wereobserved during thawing following both rapid and slow cooling. Following cooling in dimethylsulphoxide cells of C. brebissoniiwere protected against freezing injury. The recovery on thawingfrom –196?C being determined by the rate of cooling, anoptimum rate of 1?C min^–1 was observed. During slow ratesof cooling (<2?C min^–1) cells remained unshrunken,at faster rates (10?C min^–1) the loss of cell viabilitywas related to osmotic shrinkage during cooling rather thanto nucleation of intracellular ice. Intracellular ice formationwas observed only following significantly faster rates of cooling(>20?C min^–1). Key words: Cylindrocystis, Micrasterias, cryomicroscopy, freezing injury     

Effect of High Temperature on the Development of Cyanide-Sensitive Respiration in the Germination Process of Spinach Seeds

Germination of spinach (Spinacia oleracea L. var. grabra cv.Nobel) seeds was inhibited at a high temperature (35?C). Effectsof KCN on the respiration of seeds incubated at 20 and 35?Cwere compared in order to investigate the mechanism of inhibitionof seed germination by high temperature. Respiration of germinatingseeds incubated at 20?C was inhibited about 50% by 5 mM. KCNsolution, whereas it hardly inhibited the weak respiration ofthe seeds at 35?C. Germination of seeds was delayed by exogenousKCN. When the KCN solution was renewed daily, germination wascompletely inhibited. Pericarp removal promoted germinationat 35?C, but atypical germination (cotyledons emerging earlierthan a radicle) took up more than half of the total germination.The inhibitory action of KCN on the respiration of seeds wasnot altered by pericarp removal. A KCN addition, even at 20?C,elicited atypical germination in the pericarp-less seeds. Theseresults show that cyanide-sensitive respiration is needed toinduce typical spinach seed germination (root emergence), butis rendered inoperative by high temperatures thus bringing aboutpoor germination and atypical germination. (Received December 1, 1984; Accepted February 8, 1985)     

The Effect of Temperature on Photosynthesis and Carbon Fluxes in Sunflower and Rape

Sunflower (Helianthus annuusL.) and oilseed rape (Brassica napusL.) were grown at constant temperatures of 30 ?C (warm) and13 ?C (cold). Maximal rates of photosynthesis between 5 ?C and35 ?C were at higher temperatures in sunflower than rape. Photosyntheticrate over 4 h at the growth temperature declined in warm-andcold-grown rape and cold-grown sunflower, but remained constantin warm-grown sunflower. The stimulation of photosynthesis by2.0 kPa O₂ compared to 21 kPa O₂ declined with decreasing temperature.At 10 ?C in warm-grown rape photosynthesis was insensitive to2.0 kPa O₂. However, sensitivity to low O₂ continued at 10 ?Cin warm-grown sunflower. Carbohydrates accumulated in the cold,particularly fructose, glucose and sucrose in warm-grown sunflowertransferred to 13 ?C. By monitoring changes of ¹⁴C in leaves after the assimilationof ¹⁴CO₂, the rates of carbon export from leaves, pool sizesand carbon fluxes between them were estimated. The transferof warm- and cold-grown rape to 13 ?C and 30 ?C, respectively,had little effect on these parameters over 22 h. However, exportof carbon from sunflower leaves at 13 ?C was markedly less thanat 30 ?C, irrespective of the growth temperature, due to slowerexport from the transport pool. The rapid suppression of carbonexport at 13 ?C in warm-grown sunflower may be due to inhibitedtranslocation rather than reduced sink demand in the cold. It is concluded that assimilate utilisation is more depressedin the cold than is photosynthesis; this imposes a greater restrictionon biomass production in sunflower than in rape. Key words: Sunflower, rape, temperature, photosynthesis, carbon fluxes     

Effects of two free radical scavengers and intermittent warming on chilling injury and polar lipid composition of cucumber and sweet pepper fruits

Cucumber (Cucumis sativus L.) and sweet pepper (Capsicum annuumL.) fruits were chilled at 2.5?C for different periods and thentransferred to 20?C and subsequently evaluated for chillinginjury. Sodium benzoate at 10 nw or ethoxyquin at 9.2 mM, appliedas a 5-min dip before chilling, increased the degree of unsaturationof 18-carbon fatty acids in the polar lipids and reduced theseverity of chilling injury. Intermittent warming to 20?C for24 hr at 3-day intervals also alleviated the chilling symptomsand increased fatty acid unsaturation of the polar lipids incucumber and pepper fruits. (Received August 22, 1978; )     

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     

Effect of Temperature and External pH on the Cytoplasmic pH of Chara corallina

Cytoplasmic pH (pH_c) in Chara corallina was measured (from [¹⁴C]stribution)as a function of external pH (pH₀)and temperature. With pH₀near 7, pH_c at 25?C is 7.80; pH_cincreases by 0.005 pH units?C^–1 temperature decrease, i.e. pH_c at 5 ?C is 7.90. WithpH? near 5.5, the increase in pH_c with decreasing temperatureis 0.015 units ?C^–1 between 25 and 15?C, but 0.005 units?C^–1 between 15 and 5?C. This implies a more precise regulationof pH_c with variations in pH_o at 5 or 15 ?C compared with 25?C. The observed dp H_c/dT is generally smaller than the –0.017units ?C^–1 needed to maintain a constant H⁺/OH^–1,or a constant fractional ionization of histidine in protein,with variation in temperature. It is closer to that needed tomaintain the fractional ionization of phosphorylated compoundsor of CO₂–HCO₃^– The value of dpH_c/dT has importantimplications for several regulatory aspects of cell metabolism.These include (all as a function of temperature) the rates ofenzyme reactions, the _H+ at the plasmalemma(and hence the energy available for cotransport processes),and the mechanism for pH_c regulation by the control of bidirectionalH⁺ fluxes at the plasmalemma.     

Two photophobic responses in Volvox carteri

Phototaxis of Volvox carteri is the result of two photophobicresponses: stop and accelerationof flagellar activity in theanterior region of the colony. These responses of a colony fixedunder a microscope were analyzed quantitatively by cine-micrography. The phototactic sign of Volvox is temperature-dependent: itis positive at room temperature and negative at low temperature.When the temperature was lowered, the stop response to the on-stimuluswas reduced and changed to the acceleration response, whilethe acceleration response to the off-stimulus changed to thestop response. Decrease in light inteasity resulted in reduction in both stopresponses, i.e., the response to the on-stimulus at 24?C andthat to the off-stimulus at 16?C, but scarcely affected theacceleration responses. The action spectra of the photophobic responses at 24? and 14?Care similar, with a peak at 520 nm. (Received January 24, 1979; )     

Alteration of the respiratory function in chill-sensitive callus due to low temperature stress: Involvement of the alternate pathway

The diversion of electron flow to the alternate pathway in mitochondriaof chillsensitive callus of Cornus stolonifera was studied withreference to the immediate response of the cells to chilling.Temperatures below 15?C diverted the bulk of respiration tothe alternate path, proportionally as the temperature decreasedto 0?C. The alternate path, however, existed in cells in a suppressedform at temperatures above 15?C. In chill-resistant callus ofSambucus Sieboldiana, no alteration was noted in electron apportionmentbetween the cytochrome path and the alternate path. Thus, thereseems to be a marked difference in the mode of respiration betweensensitive and resistant plant cells at low temperatures. Therespiratory control ratio also markedly declined at temperaturesbelow 15?C in chill-sensitive callus, but a higher respiratorycontrol ratio was observed below 10?C in chill-resistant callus.From these results, an alteration in the regulatory system forelectron apportionment between the two paths is probably themost immediate response of chill-sensitive cells to low temperatures. ¹Contribution No. 2154 from the Institute of Low TemperatureScience. (Received June 6, 1979; )