STUDIES OF CARBON AND NITROGEN METABOLISM BY THREE MARINE PHYTOPLANKTON SPECIES IN NITRATE-LIMITED CONTINUOUS CULTURE1,2

Characteristics of carbon production, excretion and dark respiration, and nitrate uptake kinetics were studied using continuous culture techniques for Thalassiosira allenii Takano, Monorhrysis lutheri Droop and Dunaliella tertiolccta Butcher. Fur T. allenii. the ratio of dark C loss to daytime net C production varied between 0.1 and 0.2 over a growth rate range from ca. 0.005 to 0.06 h^-1. For M. lutheri and D. tertiolecta. this same ratio varied belween 0.2 and 0.3 between growth rates of ca. 0.005 and 0.025 h^-1, but declined at higher growth rates when the dark nitrate uptake capacity of the cells was exceeded by the pumping rate. Carbon excretion rates averaged less than 1.5% of daytime net C production rates. Productivity indices showed little correlation with growth rate, due to the significant poisitive correlation between chl a:C ratios and growth rate. Chlorophyll a:C ratios for T. allenii were less than 0.01 al growth rates less than 0.03 h^-1, and appoached zero at zero growth rate. Dark nitrate maximum uptake rates for M. lutheri, D. tertiolecta and T. allenii averaged 23, 64 and 120%, respectively, of light nitrate maximum uptake rates. Excretion of nitrite was observed during most nitrate uptake experiments. This excretion reduced net uptake of nitrate spikes in the dark for M. lutheri and D. tertiolecta by 79 and 23%, respectively.     

Growth characteristics of the cyanobacterium Nostoc flagelliforme in photoautotrophic, mixotrophic and heterotrophic cultivation

Nostoc flagelliforme is a terrestrial cyanobacterium with high economic value. Dissociated cells separated from a natural colony of N. flagelliforme were cultivated for 7 days under either phototrophic, mixotrophic or heterotrophic culture conditions. The highest biomass, 1.67 g L⁻¹ cell concentration, was obtained under mixotrophic culture, representing 4.98 and 2.28 times the biomass obtained in phototrophic and heterotrophic cultures, respectively. The biomass in mixotrophic culture was not the sum as that in photoautotrophic and heterotrophic cultures. During the first 4 days of culture, the cell concentration in mixotrophic culture was lower than the sum of those in photoautotrophic and heterotrophic cultures. However, from the 5th day, the cell concentration in mixotrophic culture surpassed the sum of those obtained from the other two trophic modes. Although the inhibitor of photosynthetic electron transport DCMU [3-(3,4-dichlorophenyl)-1,1-dimethylurea] efficiently inhibited autotrophic growth of N. flagelliforme cells, under mixotrophic culture they could grow by using glucose. The addition of glucose changed the response of N.flagelliforme cells to light. The maximal photosynthetic rate, dark respiration rate and light compensation point in mixotrophic culture were higher than those in photoautotrophic cultures. These results suggest that photoautotrophic (photosynthesis) and heterotrophic (oxidative metabolism of glucose) growth interact in mixotrophic growth of N. flagelliforme cells.     

Nutritional characteristics of a mixotrophic nanoflagellate,Ochromonas sp.

Autotrophic and heterotrophic growth characteristics of a nano-flagellate were investigated. The flagellate,Ochromonas sp., was isolated from the northern Baltic Sea. Autotrophic growth was poor. Axenically pregrown flagellates did not increase significantly in cell number during incubation in different inorganic media. The number of flagellates remained constant 3–5 weeks in cultures kept in the light (100mol m^–2 sec^–1), whereas in the dark, a high mortality rate was found. Uptake of inorganic¹⁴C into an acid-stable fraction indicated thatOchromonas had a functional photosynthetic apparatus. Heterotrophic growth in both liquid medium and medium containing bacteria was rapid. The maximum growth rate corresponded to a generation time of 5.3 hours. Light had no effect on heterotrophic growth. Cells pregrown onEscherichia coli minicells survived without additional bacteria as food when kept in the light, but rapid death occurred in darkness. In conclusion, heterotrophy is the major mechanism to support growth in this species ofOchromonas, but under poor environmental conditions photoautotrophy might be a strategy for survival rather than growth.     

RATES OF PHOTOSYNTHESIS AND RESPIRATION OF THE MOSS BRYUM SANDBERGII AS INFLUENCED BY LIGHT INTENSITY AND TEMPERATURE

Using differential respirometry and air enriched to 3% CO₂ (v/v), the rates of photosynthesis and dark respiration of the moss Bryum sandbergii were measured as influenced by temperature and light intensity. The optimal temperature for net (apparent) photosynthesis was between 24 to 30 C; however, the photosynthesis/respiration ratio was about 11 to 27 between 4 to 24 C and dropped to lower values at 34 C., which indicates a wide temperature tolerance for this moss in short-term experiments. The maximum temperature for photosynthesis was about 41 C and the minimum was below –5 C. At 20 C light saturation was approached at 6.2 mw cm^–2 (ca. 700 ft-c) but not completely reached at 12 mw cm^-2; the light compensation point was estimated to be 0.4 mw cm^-2 (ca. 40 ft-c). At 4 C light saturation and the compensation point were at lower levels and apparently solarization occurred at 12 mw cm^-2. Light intensity had little or no apparent effect on dark respiration. However, respiration increased with temperature over various ranges extending from –5 to 39 C with temperature quotients of about 2.5 to 1.2. The significance of these characteristics is discussed with respect to the ecological relationships of the species.     

NUTRITION OF PANDORINA MORUM1,2

A defined medium was developed for 3 strains of Pandorina morum. The strains tested required no vitamins or other organic compounds. The optimal initial pH was between 7.0 and 8.0. Various carbon sources were tested, and only glycolate and acetate appreciably stimulated growth. Mixotrophic growth in the light was stimulated by glycolate in all 3 strains, and by acetate in strains 880 and N76-6. Only strain N76-6 utilized acetate for heterotrophic growth in the dark. Thirty strains of P. morum of world-wide distribution were surveyed for mixotrophic and heterotrophic growth with acetate. All were found to fit 1 of 3 classes with respect to acetate metabolism: (1) no effect in light or dark; (2) stimulation of growth in light only; (3) stimulation of growth in light and dark.     

Light control of the respiration of exogenous glycerol in the red macroalga Grateloupia doryphora

Heterotrophic activity in macroalgae has been little studied, but the red macroalga Grateloupia doryphora is known to grow in light at a higher rate in a glycerol-containing medium than in seawater. The effects of 0·1 M exogenous glycerol in seawater (SW90-gly) on the respiration rate of G. doryphora and the role played by light were investigated. The algae pretreated for 2 h in the light and in SW90-gly evolved oxygen and fixed carbon dioxide (H¹⁴CO₃ ^?), but also evolved radioactive ¹⁴CO₂ from [¹⁴C]glycerol. The rate of oxygen evolution was lower than that of samples in seawater, due to a high respiration rate and/or a partial inhibition of photosynthesis induced by glycerol. In contrast, the rate of inorganic carbon fixation was higher in SW90-gly than in control samples in seawater, suggesting that non-photosynthetic patterns were operating. In darkness, after pretreatment in the light in SW90-gly, samples showed a high oxygen uptake rate just after the light was turned off. Twenty minutes of darkness were enough to decrease this high respiration rate to that of samples in seawater. The oxygen uptake observed in all experiments with glycerol was mitochondrial as it was inhibited by potassium cyanide and salicylhydroxamic acid (SHAM). Pretreatment of samples in the light in SW90-gly with the photosynthetic inhibitor DCMU did not inhibit ensuing dark respiration, thus providing evidence for a non-photosynthetic effect of the light. The highest dark respiration rate was observed after the samples were pretreated in monochromatic blue light in glycerol-containing media.     

Osservazioni Sull'effetto Inibente di Elevate Pressioni Osmotiche su Diversi Tipi di Crescita

Abstract

On the inhibition of seeds germination and of growth by cell enlargement by the osmotic pressure of the medium. — The mechanism of inhibition by osmotic pressure (O.P.) of the medium on growth and respiration of germinating wheat, castor bean and lettuce sèeds and of etiolated pea internode segments was investigated.

The following results were obtained:

1 - External osmotic pressure (up to 0.3 M) of various substances such as mannitol, urea, glucose, NaCl, was shown to inhibit the germination and growth of lettuce, wheat and castor bean seeds.

2 - a) A remarkable decrease of the development of respiration during the first 48 h of germination was demonstrated in embryos of wheat seeds germinated and maintained in mannitol solutions at concentration from 0,2 to 0,3 M.

b) A slight but reproducible inhibition of óxygen uptake by O.P. was also observed in embryos isolated from wheat seeds germinated in water for 24 and 34 h and transported respectively in water or into 0,2 M mannitol solutions.

This is interpreted as indicating that high external O.P. inhibits both the respiratory metabolism and the development with time of enzyme systems supporting respiration.

3 - Mannitol solutions (0,2–0,3 M) inhibited completely growth by cell enlargement in pea internode sections, while they did not at all affect oxygen uptake and protein synthesis ( ¹⁴ C - leucine incorporation). The stimulatory effect of auxin on pea elongation was almost completely suppressed by mannitol, whereas the hormone stimulation of respiration remained unchanged.

These data are interpreted as indicating that in tissues, presenting an advanced differentiation, high external O.P. inhibits growth by a direct physico-chemical mechanism; while the inhibitory effect in embrional tissues seems to comprehend, besides this direct effect, a complicated metabolic component, apparently influencing protein synthesis.     

Responses of Heterotrophic Cultures of Chlorella vulgaris Beyerinck to Darkness and Light. II. Action Spectrum for and Mechanism of the Light Requirement for Heterotrophic Growth

Chlorella vulgaris Beyerinck (Emerson's strain), fails to grow in the dark even when sugars are provided. This phenomenon was clearly demonstrated in the alga, C. vulgaris, for which the growth rate in darkness on a glucose medium remained constant for 2 days and then declined to approach zero. Pigment concentrations also declined in darkness. Changes in flow rate of 1% CO₂-in-air from zero to 7 ml per minute caused a progressive increase in the dark growth rate over a 5-day period, but did not maintain growth in the dark. Rates above 7 ml per minute produced no changes in growth rates.

White light intensities below the compensation point of the alga maintained heterotrophic growth. The saturation value for this response was 0.8 μw/cm². White light also initiated growth in nongrowing cultures transferred from darkness to light.

The action spectrum for heterotrophic growth indicated a porphyrin as the active pigment. Light in the 425 mμ region was 4 times as effective as white light in stimulating heterotrophic growth. A secondary peak of growth stimulation occurred in the 575 mμ region.

The respiration of glucose by the alga was stimulated by low intensities of white light. This response was not immediate, but was clearly present after the third day of incubation.

Malonate and cyanide were inhibitory to growth of C. vulgaris on inorganic medium or glucose medium under 300 ft-c of white light. These data suggested that succinic dehydrogenase and cytochrome oxidase systems were present.

Substances inhibitory to growth were excreted into the medium under dark-growth conditions, and 2 of these substances were indentified as formic and acetic acids.

The evidence suggested that respiration of glucose cannot proceed for an extended period of time in darkness. The reason for this is postulated to be the lack of a cytochrome or a cytochrome precursor.

     

Acetate Metabolism by an Obligate Phototrophic Strain of Pandorina morum1

SYNOPSIS. Acetate metabolism was studied in 2 strains of the green alga Pandorina morum. Both strains were capable of mixotrophic growth in the light, but only one strain was capable of heterotrophic growth in the dark. ¹⁴C-2-acetate uptake by both strains was studied in the light and dark, in the presence and absence of CO₂ and 3(3,4-dichlorophenyl)-1,1-dimethylurea (10^?5M). The distribution of radioactivity incorporated into the insoluble, aqueous and chloroform soluble fractions of the cells was determined. The strain incapable of heterotrophic growth in the dark was found to incorporate very little acetate in the dark, and its ability to incorporate acetate into the insoluble fraction was severely limited under all conditions. Incorporation into the aqueous and chloroform-soluble fractions in the light was similar in both strains. The reduced incorporation into the insoluble fraction was almost totally the result of limited incorporation of acetate into polysaccharides by the obligate phototrophic strain.     

Photosystem II and Hypoxic Quiescence in Alligatorweed

Stem cuttings of alligatorweed [Alternanthera philoxeroides (Mart.) Griseb.] were subjected to various light and chemical inhibitor treatments to obtain information about the physiological nature of the hypoxic quiescence induced by dark submergence. White or red light at 40 μE m^?2 s^?1 stimulated growth from submerged stem cuttings but far-red at 5 μE M^?2 s^?1 did not. Photo-system II inhibitors, such as 3-(3,4-dichlorophenyl) 1,1-dimethylurea (DCMU) at 1.4 × 10^?5M or 2-chloro-4,6-bis(ethylamino)-s-triazine (simazine) at 10^?5M, completely inhibited the growth that normally occurs in a submerged state under continuous white light at 40 μE m^?2 s^?1. These concentrations of DCMU or simazine did not reduce nonphotosynthetic growth from underwater nodes of emersed stem cuttings partially exposed to air in the light for 1 week. Hydrogen peroxide at 50 mg/1 added every other day partially relieved the simazine-induced inhibition of growth from submerged, illuminated cuttings. These data indicated that sprouting and early growth of submerged, illuminated alligatorweed depended on the oxygen produced by photosystem II to support respiration and to overcome hypoxic quiescence.     

Respiration in the Light and Bacterio-Phytoplankton Coupling in a Coastal Environment

In pelagic ecosystems, the principal source of organic matter is via autotrophic production and the primary sink is through heterotrophic respiration. One would therefore anticipate that there is some degree of linkage between these two compartments. Recent work has shown that respiration in the light is higher than dark respiration. Consequently, many of the methods used to determine respiration and production are biased as they require the assumption that light and dark respiration rates are equivalent. We show here that, in a coastal ecosystem, under visible light exposure, respiration in the light is related to gross production. More than 60% of the variation of respiration in the light, measured at 1 to 40 μg L⁻¹ of chlorophyll a (Chla), could be explained by the variations of gross production. Secondly, the relative contribution of bacterial respiration to community respiration in the light represented up to 79% at low Chla (1 μg L⁻¹) and was negatively correlated with Chla concentration. Although bacterial production and bacterial respiration were both enhanced in the light, bacterial respiration in the light was more stimulated than bacterial production, which resulted in a decrease in bacterial growth efficiency during light exposure. These results show that the impact of light on the functioning of the microbial loop needs to be taken into account for a better understanding of the oceanic carbon cycle.     

HETEROTROPHIC GROWTH OF ULVA LACTUCA (CHLOROPHYCEAE)1

The effect of external glucose (51 mM) and acetate (13 mM) on growth and photosynthetic capacity of Ulva lactuca L. was tested in laboratory cultures over 41 days in the dark and in dim light (0.9 μmol photons·m^?2·s^?1) at 7–8° C. Glucose and acetate had a significant positive effect on growth rate, chlorophyll content, and quantum yield for discs grown in the dark and in dim light. The carbon gain from heterotrophic uptake was low and only allowed U. lactuca to maintain a specific uptake was low and only allowed U. lactuca to maintain a specific growth rate of 0.005 day^?1 compared to 0.06–0.1 day^?1 at higher light intensities. However, plants with added organic substrate maintained a normal chlorophyll content and were able to photosynthesize whereas control plants lost pigmentation and photosynthetic capability after 41 days in both dim light and darkness, probably because of disorganization of the photosynthetic apparatus. This suggest that the ecological significance of heterotrophic uptake is to allow U. lactuca to survive during prolonged low light conditions with an intact photosynthetic apparatus.     

Photosynthetic characteristics of the shade-adapted C4 grass Muhlenbergia sobolifera (Muhl.) Trin.: control of development of photorespiration by growth temperature

Muhlenbergia sobolifera (Muhl.) Trin., a C₄ grass, occurs in understory habitats in the northeastern United States. Plants of M. sobolifera were grown at 23 and 30°C at 150 and 700 μmol photons m⁻² s⁻¹. The photosynthetic CO₂ compensation point, maximum CO₂ assimilation, dark respiration and the absorbed quantum use efficiency (QUE) were measured at 23 and 30°C at 2 and 20% O₂. Photosynthetic CO₂ compensation points ranged from 4 to 14mm³ dm⁻³ CO₂ and showed limited O₂ sensitivity. The mean photosynthetic CO₂ compensation point of plants grown at 30°C (4·5 mm³ dm⁻³) was 57% lower and 80% less inhibited by O₂ than that of plants grown at 23°C. Photosynthesis was similarly affected by growth temperature, with 70% more O₂ inhibition in plants grown at 23°C; suppression over all treatments ranging from 2 to 11%. Unlike typical C₄ species, plants of M. sobolifera from both temperature regimes exhibited higher CO₂ assimilation rates when grown at low light. Growth temperature and light also affected QUE; plants grown at low light and 23°C had the highest value (0·068 mol CO₂/mol quanta). Measurement temperature and growth light regime significantly affected dark respiration; however, O² did not affect QUE or dark respiration under any growth or measurement conditions. The results indicate that M. sobolifera is adapted to low PPFD, and that complete suppression of photorespiration is dependent upon high growth temperature.     

Trophic dependencies of some larval chironomidae (Diptera) and fish species in the River Thames

Experiments are described to characterise the heterotrophic potential of Westiellopsis prolifica Janet, which fixes nitrogen under light and dark conditions. The growth of the organism in terms of dry weight increase, was more in fructose, lactose, sucrose, sorbose, galactose, glucose, sodium acetate, mannitol, sorbitol, glycerol, ethyl alcohol and butyl alcohol, when the alga was pretreated with light and subsequently incubated with the substrates in light. Mannose, xylose, acetic acid, propionic acid, fructose 1,6 di Po₄, pyruvic acid, dihydroxyacetone and succinic acid decreased the growth of the organism in the same condition. In dark incubation after pretreatment with light, as well as in the dark, Westiellopsis showed a better growth response to almost all the exogenous substrates. However, after pretreatment either with light or dark, the test organism utilised exogenous substrates quicker in light than in dark incubations. These experiments would suggest that the substrate specificity and efficiency of substrate utilisation by the alga during its heterotrophic growth are governed by the growth conditions.     

GROWTH OF TWO FACULTATIVELY HETEROTROPHIC MARINE CENTRIC DIATOMS1,2

The facultative, heterotrophs Cyclotella cryptica (sclone WT-1-8) and Coscinodiscus sp. were selectively isolated from coastal waters by dark incubation of organically enriched solid medium. C. cryptica grows in the dark with glucose and galactose, and Coscinodiscus sp. with glucose. Clone WT-1-8 of C. cryptica grows about twice as fast with glucose as a previously studied clone (0-3A). In the dark with, 5 × 10^?6 M glucose C. cryptica divides every 3 days, while with 5 × 10^?5 M glucose Coscinodiscus sp. divides every 10 days. Heterotrophic growth of either diatom for 1 year does not cause a major reduction in carbon, nitrogen, chlorophyll a, and chlorophyll c contents, or in photosynthetic ability, compared to light-grown cells. It is possible that facultative heterotrophy is of ecological benefit to these diatoms, probably for slow growth and survival during extended periods of dim light or darkness.     

PHOSPHORUS LIMITATION AND CARBON METABOLISM IN A UNICELLULAR ALGA: INTERACTION BETWEEN GROWTH RATE AND THE MEASUREMENT OF NET AND GROSS PHOTOSYNTHESIS1

Chlamydomonas reinhardii Dangeard was grown in continuous culture under P limitation at a range of dilution rates. Carbon uptake measurements were performed using double isotope (¹²C/¹⁴C) techniques and the fluxes of carbon in the light and dark were analysed over the range of growth rates. ¹⁴C uptake was shown to be equal to gross photosynthesis only at maximum relative growth rates; at low relative growth rates ¹⁴C uptake approximated net photosynthesis. The altered pattern of C uptake was found to be due to the suppression of dark respiration in the light and the release of ¹⁴C0₂ from respiratory pathways at low relative growth rates. Metabolic channelling of ¹⁴C from photosynthetic pathways to respiratory pathways occurred at low growth rates as the specific activity of the respired CO₂ reached 45% of the input gas mixture. These data are discussed in the light of the controversy concerning the measurement of gross and net photosynthesis in natural populations and in the light of models of ¹⁴C uptake in single celled algae. Existing models are shown to be adequate for high relative growth rates but not for low relative growth rates under P limitation.     

ORGANIC CARBON SUPPLEMENTATION OF STERILIZED MUNICIPAL WASTEWATER IS ESSENTIAL FOR HETEROTROPHIC GROWTH AND REMOVING AMMONIUM BY THE MICROALGA CHLORELLA VULGARIS1

Heterotrophic growth of the microalga Chlorella vulgaris Beij. in synthetic as well as sterilized municipal wastewater of a nonindustrialized city was measured. The city wastewater contained high levels of ammonium and nitrate, medium levels of phosphate, and low levels of nitrite and organic molecules and could not support heterotrophic growth of C. vulgaris. Evaluation of 11 known carbon sources for this microalga that were added to standard synthetic wastewater containing the same levels of nitrogen and phosphorus as the municipal wastewater revealed that the best carbon sources for heterotrophic growth were Na‐acetate and d ‐glucose. These provided the highest growth rates and the largest removal of ammonium. Growth increased with concentration of the supplement to an optimum at 0.12 M Na‐acetate. This carbon source was consumed completely within 10 d of incubation. Higher concentrations inhibited the growth of C. vulgaris. The microalgal populations under heterotrophic growth conditions were one level of magnitude higher than that under autotrophic growth conditions that served as a comparison. No growth occurred in the dark in the absence of a carbon source. Na‐acetate was superior to d ‐glucose. In municipal wastewater, when Na‐acetate or d ‐glucose was added, C. vulgaris significantly enhanced ammonium removal under heterotrophic conditions, and its capacity was equal to ammonium removal under autotrophic growth conditions. This study showed that sterilized wastewater can be treated by C. vulgaris under heterotrophic conditions if supplemented with the appropriate organic carbon source for the microalgae.     

16O2/18O2 analysis of oxygen exchange in Dunaliella tertiolecta. Evidence for the inhibition of mitochondrial respiration in the light

A mass spectrometric ¹⁶O₂/¹⁸O₂-isotope technique was used to analyse the rates of gross O₂ evolution, net O₂ evolution and gross O₂ uptake in relation to photon fluence rate by Dunaliella tertiolecta adapted to 0.5, 1.0, 1.5, 2.0 and 2.5 M NaCl at 25°C and pH 7.0.At concentrations of dissolved inorganic carbon saturating for photosynthesis (200 M) gross O₂ evolution and net O₂ evolution increased with increasing salinity as well as with photon fluence rate. Light compensation was also enhanced with increased salinities. Light saturation of net O₂ evolution was reached at about 1000 mol m^-2s^-1 for all salt concentrations tested. Gross O₂ uptake in the light was increased in relation to the NaCl concentration but it was decreased with increasing photon fluence rate for almost all salinities, although an enhanced flow of light generated electrons was simultaneously observed. In addition, a comparison between gross O₂ uptake at 1000 mol photons m^-2s^-1, dark respiration before illumination and immediately after darkening of each experiment showed that gross O₂ uptake in the light paralleled but was lower than mitochondrial O₂ consumption in the dark.From these results it is suggested that O₂ uptake by Dunaliella tertiolecta in the light is mainly influenced by mitochondrial O₂ uptake. Therefore, it appears that the light dependent inhibition of gross O₂ uptake is caused by a reduction in mitochondrial O₂ consumption by light.Abbreviations DCMU 3-(3, 4-dichlorophenyl)-1, 1-dimethylurea - DHAP dihydroxy-acetonephosphate - DIC dissolved inorganic carbon - DR_a rate of dark respiration immediately after illumination - DR_b rate of dark respiration before illumination - E₀ rate of gross oxygen evolution in the light - NET rate of net oxygen evolution in the light - PFR photon fluence rate - RubP rubulose-1,5-bisphosphate - SHAM salicyl hydroxamic acid - U₀ rate of gross oxygen uptake in the light     

IAA-induced opening of excisedMimosa pulvinules

Movement ofMimosa pudica L. pulvinules was investigated by using excised ones which were placed on a moist filter paper. The pulvinules excised in the morning opened at the addition of IAA (10⁻⁷ M to 10⁻⁴M) in the dark. The lag period for the onset of the opening was about 15 min. Na-acetate buffer (pH 4) also induced the opening of pulvinules in the dark, and the buffer-induced opening was inhibited by the uncouplers of oxidative phosphorylation. Na-MES and Na-citrate buffers (pH 4) did not induce the opening. Pulvinules taken from closed leaves in the evening were less responsive to IAA than those taken from open leaves in the morning. The pulvinules taken in the evening slightly opened with incandescent light (4000 lux), but those preincubated with IAA (10⁻⁷M and 10⁻⁶M) opened distinctly upon the illumination.     

GERMINATION OF LIGHT-INHIBITED SEED OF NEMOPHILA INSIGNIS

Germination of Nemophila insignis seed is inhibited by light over a wide range of temperatures. At low temperatures the light intensity required for inhibition is higher. At 25 C there is little germination (in darkness as well as in light); at 27.5 C germination is inhibited altogether. Virtually complete germination in light is obtained when the endosperm directly covering the radicle is removed. This operation also improves germination in darkness at 25 C. Mechanical scarification performed elsewhere in the seed is without effect. As with Phacelia tanacetifolia, Nemophila seed apparently fails to germinate in light because the endosperm restrains the expansive growth of the embryo. The embryo of dark-imbibed seed develops a force which enables it to overcome the physical resistance of the endosperm. Light inhibits the process which leads to generation of “expansive force.” Gibberellic acid at 5 × 10^–4 m stimulates germination in light and in the dark. Abscisic acid at 10^-4 m inhibits germination; at 10^-6 m it inhibits only root growth. The inhibition of germination or root growth caused by abscisic acid cannot be reversed by gibberellic acid. Eighty per cent oxygen under certain conditions promotes germination. The rate of O₂ uptake is enhanced in oxygen-enriched atmosphere; however, there is no corresponding increase in the rate of CO₂ output. Thus high oxygen tension enhances an oxidative process other than respiration. This reaction is favorable to seed germination.