EFFECTS OF FLOWING WATER ON NITROGEN- AND PHOSPHORUS-LIMITED PHOTOSYNTHESIS AND OPTIMUM N:P RATIOS BY SPIROGYRA FLUVIATILIS (CHAROPHYCEAE)1,2

The effects of flowing water on net photosynthesis, dark respiration, specific growth rate, and optimum N:P ratios by Spirogyra fluviatilis Hilse were assessed. The alga was cultivated under nitrogen or phosphorus limitation in laboratory streams at three flow velocities: 3, 12, and 30 cm·s^?1. The Droop equation adequately described respiration and photosynthesis (PS_net) as a function of N or P cell quota (Q^N or Q^p). The data show that for N- or P-limited Spirogyra fluviatilis, flowing water is physiologically costly. Generally, flowing water had little effect on respiration rates; however, the proportion of gross photosynthesis devoted to dark respiration did increase with flow velocity. For photosynthesis, the minimum N and P cell quotas increased with velocity, and the theoretical PS_net maxima for N and P both appeared greatest at 12 cm·s^?1. The Droop models showed that for any given Q^N or Q^p, PS_net, was reduced by the 30-cm·s^?1 treatment. Consistent with this finding, independent estimates of specific growth rates for P-limited S. fluviatilis in the laboratory streams were inversely related to flow velocity when ambient PO₄^?3 was undetectable. However, growth was not diminished at the fastest velocity when PO₄^?3 was available for uptake. Thus, the increase in cellular phosphorus demand can be offset by flow-enhanced P uptake when conditions permit; otherwise, growth will be impaired. The optimum N:P ratios for S. fluviatilis at 3, 12, and 30 cm·s^?1 were 50, 58, and 52 by atoms, respectively, when calculated for PS_net= 0. The optimum ratios were inversely related to PS_net and decreased to approximately 20 when PS_net was near maximum. The potential for flowing water to mediate nutrient partitioning among lotic algae by altering growth rates and optimum nutrient ratios is discussed.     

Photosynthesis and respiration in bladelets of Ecklonia cava Kjellman (Laminariales, Phaeophyta) in two localities with different temperature conditions

Characteristics of photosynthesis and respiration of bladelets were compared between Ecklonia cava Kjellman sporophytes growing in a warmer temperate locality (Tei, Kochi Pref., southern Japan) and in a cooler temperate locality (Nabeta, Shizuoka Pref., central Japan). Photosynthesis and respiration were measured with a differential gas-volumeter (Productmeter). In photosynthesis-light curves at 20°C, the rate of net photosynthesis was almost the same at light intensities lower than 25 μmol m⁻² s⁻¹ and the light-saturation occurred at 200–400 μmol m⁻²s⁻¹ in plants of both localities. The light-saturated net photosynthetic rates were higher in winter and spring than in summer and autumn in both plants. The optimum temperature for net photosynthesis at 400 μmol m⁻²s⁻¹ was 27°C throughout the year in the Tei plant and 25–27°C in the Nabeta plant. The decrease of net photosynthetic rates in the supraoptimal temperature range up to 29°C was sharper in winter and spring than in summer and autumn in both plants, being smaller in the Tei plant than in the Nabeta plant in all seasons. The dark respiration rate always increased with water temperature rise in both plants. No clear differences were found in the dark respiration rate between Tei and Nabeta plants except that when measured against dry weight, the Tei plant showed a slightly lower rate as compared with the Nabeta plant.     

Effects of Variations in Daylength and Temperature on Net Rates of Photosynthesis, Dark Respiration, and Excretion by Isochrysis galbana Parke

The effects of variable daylength and temperature on net rates of photosynthesis, dark respiration, and excretion of a unicellular marine haptophyte, Isochrysis galbana Parke, were examined and related to division rates. Six combinations of daylength (18:6, 12:12, 6:18 light:dark, LD) and temperature (20, 25 C) were used. Daily rates of net photosynthesis were closely correlated to division rates, suggesting a direct relationship, and were maximal when cells were grown at 12:12 LD at both temperatures and 18:6 LD at 20 C. A daylength of 6 hours decreased daily rates by decreasing the time for carbon uptake. Further, cells grown with this daylength had maximal chlorophyll a contents, suggesting a physiological adaptation by photosynthetic units to short light periods. A photoperiod of 18:6 LD at 25 C decreased daily rates of net photosynthesis by reducing the hourly rate of net photosynthesis via an unidentified mechanism. The importance of rates of net dark respiration in controlling daily net photosynthesis was small, with carbon lost during dark periods varying between 4 and 14% of that gained during light periods. Also, the influence of net excretion was small, varying between 1.0 and 5.5% of daily net photosynthesis.     

Response of wheat canopy CO2 and water gas-exchange to soil water content under ambient and elevated CO2

The nature of the interaction between drought and elevated CO₂ partial pressure (pC_a) is critically important for the effects of global change on crops. Some crop models assume that the relative responses of transpiration and photosynthesis to soil water deficit are unaltered by elevated pC_a, while others predict decreased sensitivity to drought at elevated pC_a. These assumptions were tested by measuring canopy photosynthesis and transpiration in spring wheat (cv. Minaret) stands grown in boxes with 100 L rooting volume. Plants were grown under controlled environments with constant light (300 µmol m^?2 s^?1) at ambient (36 Pa) or elevated (68 Pa) pC_a and were well watered throughout growth or had a controlled decline in soil water starting at ear emergence. Drought decreased final aboveground biomass (?15%) and grain yield (?19%) while elevated pC_a increased biomass (+24%) and grain yield (+29%) and there was no significant interaction. Elevated pC_a increased canopy photosynthesis by 15% on average for both water regimes and increased dark respiration per unit ground area in well‐watered plants, but not drought‐grown ones. Canopy transpiration and photosynthesis were decreased in drought‐grown plants relative to well‐watered plants after about 20–25 days from the start of the drought. Elevated pC_a decreased transpiration only slightly during drought, but canopy photosynthesis continued to be stimulated so that net growth per unit water transpired increased by 21%. The effect of drought on canopy photosynthesis was not the consequence of a loss of photosynthetic capacity initially, as photosynthesis continued to be stimulated proportionately by a fixed increase in irradiance. Drought began to decrease canopy transpiration below a relative plant‐available soil water content of 0.6 and canopy photosynthesis and growth below 0.4. The shape of these responses were unaffected by pC_a, supporting the simple assumption used in some models that they are independent of pC_a.     

Effect of irradiance and temperature on the photosynthesis of a cultivated red alga,Pyropia tenera (= Porphyra tenera), at the southern limit of distribution in Japan

The effect of irradiance and temperature on the photosynthesis of the red alga, Pyropia tenera, was determined for maricultured gametophytes and sporophytes collected from a region that is known as one of the southern limits of its distribution in Japan. Macroscopic gametophytes were examined using both pulse‐amplitude modulated fluorometry and/or dissolved oxygen sensors. A model of the net photosynthesis–irradiance (P‐E) relationship of the gametophytes at 12°C revealed that the net photosynthetic rate quickly increased at irradiances below the estimated saturation irradiance of 46 μmol photons m^?2 s^?1, and the compensation irradiance was 9 μmol photons m^?2 s^?1. Gross photosynthesis and dark respiration for the gametophytes were also determined over a range of temperatures (8–34°C), revealing that the gross photosynthetic rates of 46.3 μmol O₂ mg_chl‐a^?1 min^?1 was highest at 9.3 (95% Bayesian credible interval (BCI): 2.3–14.5)°C, and the dark respiration rate increased at a rate of 0.93 μmol O₂ mg_chl‐a^?1 min^?1°C^?1. The measured dark respiration rates ranged from ?0.06 μmol O₂ mg_chl‐a^?1 min^?1 at 6°C to ?25.2 μmol O₂ mg_chl‐a^?1 min^?1 at 34°C. The highest value of the maximum quantum yield (Fv/Fm) for the gametophytes occurred at 22.4 (BCI: 21.5–23.3) °C and was 0.48 (BCI: 0.475–0.486), although those of the sporophyte occurred at 12.9 (BCI: 7.4–15.1) °C and was 0.52 (BCI: 0.506–0.544). This species may be considered well‐adapted to the current range of seawater temperatures in this region. However, since the gametophytes have such a low temperature requirement, they are most likely close to their tolerable temperatures in the natural environment.     

Remarks on mixotrophic and autotrophic carbon nutrition of Vitis plantlets cultured in vitro

Two Vitis species were cultured in vitro under photoautrophic (sucrose-free culture medium) and photomixotrophic (sucrose 15 g l^-1) conditions during the period following microcutting rooting (day 34 to day 120). Several parameters were measured at the end of the culture: growth, plant dry weight, carbohydrate uptake from the medium and rates of photosynthesis and dark respiration. The two species behaved very differently. Under photoautotrophic conditions, dark respiration, net photosynthesis and daily CO₂ fixation were higher in Vitis vinifera than in Vitis rupestris. Culture under mixotrophic conditions caused increase in growth, respiration and photosynthesis in Vitis rupestris. In contrast, photosynthesis decreased in Vitis vinifera under the same conditions.     

Variation in leaf respiration in relation to growth and photosynthesis of Lolium

Six Lolium genotypes with contrasting apparent photorespiration and CO_a compensation concentration, [C0₂]_c, were compared for net photosynthesis, dark respiration, leaf starch accumulation, rate of leaf expansion and shoot regrowth. Plants were grown in day/night temperatures of 15/10 and 25/20 ^oC. There were significant (P < 0–05) differences between the genotypes in all these parameters. At 25/20 ^oC apparent photorespiration was correlated with [CO₂]_c. Correlation coefficients, pooled from both temperature regimes, revealed that genotypes with high rates of net photosynthesis accumulated more leaf starch during light periods than genotypes with slow photosynthesis, but rates of leaf expansion and dry matter increase were only correlated, negatively, with dark respiration. Apparent photorespiration was negatively correlated with dark respiration. These findings suggest that attributes related to photorespiration such as [CO₂]_c and O₂ uptake from CO₂-free air in the light are unlikely to be useful selection criteria for growth of C₃ grasses, that net photosynthesis was probably not limiting growth and that maintenance respiration may have been an important determinant of genotypic differences in growth rate. Selections for slow and fast rates of dark respiration of mature leaves were therefore made at 8 and at 25 ^oC from within two different populations of L. perenne, S.23. This characteristic showed repeatabilities (broad-sense heritability) of from 0–41 to o-66. Six independent comparisons of simulated swards of the slow- and fast-respiring selections were made under periodic cutting regimes, either in a growth room at 25 ^oC or in a glasshouse from August to May. Growth of all plots of slow-respiring genotypes was consistently more rapid than that of the fast-respiring, at 25 ^oC in the growth room, and during autumn and spring in the glasshouse. There was no difference in winter growth. The implications of these results for the use of gas exchange measurements as selection criteria in plant breeding programmes are discussed.     

A coral polyp model of photosynthesis, respiration and calcification incorporating a transcellular ion transport mechanism

A numerical simulation model of coral polyp photosynthesis, respiration and calcification was developed. The model is constructed with three components (ambient seawater, coelenteron and calcifying fluid), and incorporates photosynthesis, respiration and calcification processes with transcellular ion transport by Ca-ATPase activity and passive transmembrane CO₂ transport and diffusion. The model calculates dissolved inorganic carbon and total alkalinity in the ambient seawater, coelenteron and calcifying fluid, dissolved oxygen (DO) in the seawater and coelenteron and stored organic carbon (CH₂O). To reconstruct the drastic variation between light and dark respiration, respiration rate dependency on DO in the coelenteron is incorporated. The calcification rate depends on the aragonite saturation state in the calcifying fluid (Ωa _cal). Our simulation result was a good approximation of “light-enhanced calcification.” In our model, the mechanism is expressed as follows: (1) DO in the coelenteron is increased by photosynthesis, (2) respiration is stimulated by increased DO in the light (or respiration is limited by DO depletion in the dark), then (3) calcification increases due to Ca-ATPase, which is driven by the energy generated by respiration. The model simulation results were effective in reproducing the basic responses of the internal CO₂ system and DO. The daily calcification rate, the gross photosynthetic rate and the respiration rate under a high-flow condition increased compared to those under the zero-flow condition, but the net photosynthetic rate decreased. The calculated calcification rate responses to variations in the ambient aragonite saturation state (Ωa _amb) were nonlinear, and the responses agreed with experimental results of previous studies. Our model predicted that in response to ocean acidification (1) coral calcification will decrease, but will remain at a higher value until Ωa _amb decreases to 1, by maintaining a higher Ωa _cal due to the transcellular ion transport mechanism and (2) the net photosynthetic rate will increase.     

Field measurement of net photosynthesis of mosses at Langhovde,East Antarctica

Net photosynthesis and dark respiration (CO₂ flux) of Antarctic mosses were measured at Langhovde, East Antarctica, from 9 to 17 January 1988. Moss blocks were taken from communities in the Yukidori Valley (69°14′30″S, 39°46′00″E) at Langhovde. Each block was composed ofCeratodon purpureus andBryum pseudotriquetrum, orB. pseudotriquetrum. The upper part of the block was used to measure net photosynthesis and dark respiration. The net photosynthesis of each sample was measured in the field for one or three days with two infrared CO₂ gas analyzers and an assimilation chamber. The relationships of net photosynthetic rate and dark respiration rate, to the water content of the sample, the intensity of solar radiation and the moss temperature were estimated from the field data. The maximum rate of net photosynthesis was about 4 μmol CO₂ m⁻²s⁻¹ at saturating radiation intensity and at optimum temperature, about 10°C. Environmental features of moss habitats in the Yukidori Valley are discussed in relation to these results.     

Leaf development and phloem transport in Cucurbita pepo: Carbon economy

Summary Net photosynthesis, dark respiration and growth for leaf 5 of Cucurbita pepo L. plants grown under controlled conditions were measured and the data used for an assessment of the changes in carbon balance during growth of the leaf through expansion to maturity. The blade is first capable of net CO₂ fixation when ca. 8% expanded but the initial rapid growth during this period is sustained almost entirely through imported nutrients. When the growth rate starts to decline rapidly the net photosynthetic capacity of the blade begins to increase. This increase is accompanied by an expansion of the intercellular spaces and by decreasing dark respiration measured at night and in dark periods during the day. The blade becomes completely independent of phloem imported nutrients and begins to export excess photosynthate when the phase of rapid decrease in relative growth rate is almost complete at about 45% expansion. Maximum net photosynthesis of ca. 11 mg CO₂ h^-1 dm^-2 is achieved at 70% expansion. The first detectable synthesis of the transport sugars stachyose and raffinose in the blade coincides with the beginning of intralaminar phloem transport from the tip to the base of the leaf. The synthesis of sucrose, the other major transport sugar, is detectable at all stages of leaf development.     

The effect of light quality and gibberellic acid (GA3) on photosynthesis and respiration rates of pea seedlings

CO₂ exchange were measured on pea seedlings (Pisum sativum L. var. Bördi) cultivated from seeds imbibed either in water (C-plants) or in gibberellic acid (GA₃) at the concentration of 25 g/1 (GA-plants), and then grown under 17 W/m² blue light (B-plants) or 11 W/m² red light (R-plants).When measured under the same light conditions as during growth the net photosynthesis (APS) rate in B-plants was about twice higher than that in R-plants. Dark respiration (DR) rate was 70% higher in B- than in R-plants. Red light retarded the development of photosynthetic activity, but GA₃ suppressed this effect. The hormone enhanced net photosynthesis and dark respiration to the same extent.When measured under saturating white light net photosynthesis rate of C-plants was also two times higher in B-plants than in R-plants. Growth conditions had only a slight effect on the APS of GA-plants under white light. APS rates of GA-plants grown under red light were higher under white light than those of C-plants, but lower than those of plants grown under blue light.We assume that blue light induced formation of plants that were adapted to higher light intensity: red light had an opposite effect, whereas gibberellic acid induced formation of plants that were adapted to medium light intensity.     

Epilithic chlorophyll a,photosynthesis, and respiration in control and fertilized reaches of a tundra stream

Photosynthesis and respiration by the epilithic community on cobble in an arctic tundra stream, were estimated from oxygen production and consumption in short-term (4–12 h), light and dark, chamber incubations. Chlorophyll a was estimated at the end of each incubation by quantitatively removing the epilithon from the cobble. Fertilization of the river with phosphate alone moderately increased epilithic chlorophyll a, photosynthesis, and respiration. Fertilization with ammonium sulfate and phosphate, together, greatly increased each of these variables. Generally, under both control and fertilized conditions, epilithic chlorophyll a concentrations (mg m⁻²), photosynthesis, and respiration (mg O₂ m⁻², h⁻¹) were higher in pools than in riffles. Under all conditions, the P/R ratio was consistent at ∼ 1.8 to 2.0. The vigor of epilithic algae in riffles, estimated from assimilation coefficients (mg O₂ [mg Chl a]⁻¹ h⁻¹) was greater than the vigor of epilithic algae in pools. However, due to the greater accumulation of epilithic chlorophyll a in pools, total production (and respiration) in pools exceeded that in riffles. The epilithic community removed both ammonium and nitrate from water in chambers. Epilithic material, scoured by high discharge in response to storm events and suspended in the water column, removed ammonium and may have increased nitrate concentrations in bulk river water. However, these changes were small compared to the changes exerted by attached epilithon.     

Changes in respiration,dry-matter production and its partition in rice (Oryza sativa L.) in response to water deficits during the grain-filling period

A simple, physiologically based model was devised and used for estimating the respiration rate and the overall conversion efficiency of photosynthate into the grain dry-matter in dehydrated plants relative to well watered controls. The model described mathematically the partitioning of assimilate produced by current photosynthesis and of assimilate stored previously between the grain and those plants parts other than grain (the “straw”). Using data obtained from the dry-matter analysis and CO₂ gas exchange measurements, the model gave us two independent estimates of the respiration rate and the overall conversion efficiency; one for the plants given a prolonged dark period and the other for those grown in a normal light and dark cycle. The rate of dark respiration increased with mild water stress: 4.3 mg g⁻¹ day⁻¹ in control plants with leaf water potential of around −0.4 MPa and 11.3 mg g⁻¹ day⁻¹ in dehydrated plants with leaf water potential of around −1 MPa, when both the control and dehydrated plants were left in the dark for ten days. Similar values were obtained for plants in a normal light and dark cycle: 5.6 in well watered and 8.1 mg g⁻¹ day⁻¹ in the stressed plants. Accordingly, the overall conversion efficiency (the ratio of grain dry-matter against the gross carbohydrate input to the construction and maintenance processes) was 0.7 to 0.8 for the well hydrated control and 0.4 to 0.5 for moderately dehydrated plants. With increasing water deficits, however, the respiration rate decreased: 4.8 mg g⁻¹ day⁻¹ when plants were severely stressed (below −3 MPa in midday leaf water potential). The decrease in straw dry weight alone overestimates dry-matter partition of the stored assimilate in the straw into grain by 20 to 30% in well watered plants and the error increases to 50 to 60% in more dehydrated plants.     

Carbon balance of Yucca elata Engelm. during a hot and cool period in situ

Respiratory activity of intact, attached roots was measured under field and controlled conditions. Root respiration of Yucca elata Engelm. was highly temperature dependent: Q₁₀ values decreased from 2.1 (12–22° C) to 1.7 (26–36° C) as temperatures increased. Respiration ceased after 5 h at 42° C. In the field, in August, when net leaf photosynthesis was severely depressed, the diel fluctuation in the respiration rate of suberized and partially suberized roots was predominantly a function of temperature. A photoperiod-associated rise in respiration rates apart from temperature response occurred in February for nonsuberized, partially suberized, and suberized roots when active net photosynthesis occurred throughout the photoperiod. In whole-plant root systems, respiratory CO₂ was 3.2 and 4.3 mg CO₂·g DW^-1·d^-1 in August and February, respectively, when adjusted for the proportion of suberized and nonsuberized lateral roots. On a whole-plant basis, 0.89 mg C·g DW^-1·d^-1 was gained during February and 0.46 mg C·g DW^-1·d^-1 was lost in August. The belowground: aboveground ratio of whole-plants in situ was 0.42 on a shallow soil where vertical root growth was limited to a soil depth of 68 cm and ranged from 1.29 to 5.94 \(\left( {\bar x = 3.31} \right)\) in deep sands. No leaf dark fixation of CO₂ was observed in field plants during August and February, nor in well-watered plants or plants subjected to drought in laboratory studies. Although small diel fluctuations in leaf acidity occurred in both field and greenhouse-grown plants, results of this study suggest that Y. elata is a C₃ plant.     

PHOTOSYNTHESIS AND PHOTOSYNTHESIS-COUPLED RESPIRATION IN NATURAL BIOFILMS QUANTIFIED WITH OXYGEN MICROSENSORS1

Photosynthesis and respiration were analyzed in natural biofilms by use of O₂ microsensors. Depth profiles of gross photosynthesis were obtained from the rate of decrease in O₂ concentration during the first few seconds following extinction of light, and net photosynthesis of the photic zone was calculated from O₂ concentration gradients measured at steady state. Respiration within the photic zone was calculated as the difference between gross and net photosynthesis. Two types of biofilms were investigated: one dominated by diatoms, and one dominated by cyanobacteria. High O₂/CO₂ ratios caused increased respiration especially within the diatom biofilm, which could indicate that photorespiration was a dominant O₂-consuming process. The rate of respiration was constant within both biofilms during the first 4.6 s following extinction of light, even when respiration was stimulated by high O₂/CO₂ ratio. The assumption of a constant rate of respiration during the dark period is an essential one for the determination of gross photosynthetic activity by use of O₂ microsensors. We here present the first evidence to substantiate this assumption. The results strongly suggest that gross photosynthesis as measured by use of O₂ microsensors may include carbon equivalents that are subsequently lost through photorespiration. Computer modeling of photosynthesis profiles measured after 1.1, 1.6, and 2.6 s of dark incubation illustrated how the actual photosynthesis profile could have appeared if it had been possible to do the determination at time 0. Diffusion of O₂ during the up to 4.6-s long dark incubations did not affect gross photosynthetic rate when integrated over all depths, but the apparent vertical distribution of the photosynthetic activity was strongly affected.     

Photosynthetic Production of a Brackish Water Community of Chara tomentosa L. and its Dependence on Environmental Conditions

Net photosynthesis and dark respiration of a natural Chara tomentosa community were continuously recorded. There is a close correlation between net rate of photosynthesis and variations in the PhAR flux under water. The net photosynthesis fluence Px correlates with the PhAR fluence Ix, but the quotient Px/Ix varies seasonally, apparently as a consequence of variations in chlorophyll content following long-range changes in radiation fluence. No influence of temperature, salinity or pH on net photosynthesis was detected, but water temperature stimulates dark respiration and consequently diminishes net primary production.     

Effects of salinity on photosynthetic characteristics in photomixotrophic cell-suspension cultures from Alternanthera philoxeroides

We studied the effect of NaCl salinity on the development of cellular photosynthesis using a green, photomixotrophic, cell-suspension culture of Alternanthera philoxeroides (Mart.) Griseb. For these cells, increasing the concentration of sucrose in the media produces a rapid drop in net photosynthetic rate, which recovers as sucrose is depleted from the media. This predictable recovery provides a simple system to examine cellular photosynthetic development. Cells, unadapted to high salinity, were transferred to nutrient media with 30 mM sucrose (Control) or nutrient media with 30 mM sucrose and 100 mM NaCl (Salt). A dramatic increase in the dark respiration rate of Control and Salt cells during the first 6 d of the experiment produced net oxygen consumption in the light. The high dark respiration rates during this period were accompanied by a decline in total Chl and the amounts of two photosynthetic proteins, the light harvesting Chl a/b binding protein of photosystem II (LHCP) and the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase (rubisco SSU). The dark respiration rate of Salt cells was greater than that of Control cells on days 4–8. After day 4, dark respiration rates decreased and net photosynthesis increased to stable values in both treatments at day 11 after media sucrose concentration reached a minimum. As dark respiration rates decreased and net photosynthetic rates increased, total Chl and the amounts of LHCP and rubisco SSU increased in both Control and Salt cells. The slower development of photosynthetic capacity in salt cells was correlated with a fresh weight that was 20% lower than that of control cells at the end of the experiment.     

Photosynthesis and respiration ofPinus pumila needles in relation to needle age and season

Rates of net photosynthesis and dark respiration were measured for detached needles ofPinus pumila trees growing on the Kiso mountain range in central Japan in 1987. Dependency of photosynthesis on light and temperature was examined in relation to needle age and season. The light saturation point of net photosynthesis was lower in 3- and 4-yr-old needles than that in current (flushed in 1987), 1- and 2-yr-old needles.P _nmax, net photosynthetic rates at 1000 μmol m⁻² s⁻¹ and 15°C, of needles from 1- to 4-yr-old generally decreased with needle age.P _nmax of 1- to 4-yr-old needles became higher in August than in other months, andP _nmax of current needles did so in September. Current needles showed high respiration rates (at 15°C) only in August. Optimum air temperatures for net photosynthesis at 1000 μmol m⁻² s⁻¹ were between 10 and 15°C for current and 1-yr-old needles. The temperature coefficient of dark respiration rates was 2.3–3.3 for current needles from August to October, and 2.2 for 1-yr-old needles in mid-July.     

The Effect of Cadmium on Net Photosynthesis, Transpiration, and Dark Respiration of Excised Silver Maple Leaves

Excised leaves of silver maple (Acer saccharinum L.) exposed to 0, 0.045, 0.090, or 0.180 mM Cd²⁴ exhibited reduced net photosynthesis and transpiration, and increased dark respiration. Rates of net photosynthesis and transpiration diminished with time and were strongly correlated with solution concentration and tissue content of Cd²⁴, Net photosynthesis and transpiration were reduced to 18 and 21%, respectively, of the untreated controls after 64 h. Dark respiration increased as much as 193% of the untreated controls but was poorly correlated with solution concentration or tissue content of Cd²⁴, Diffusive resistances of leaves to carbon dioxide and water vapor transfer increased with both increasing Cd²⁴ concentration and time. These findings are discussed in relation to stomatal function.     

Cyclic variations of photosynthetic activity under nitrogen fixing conditions in Synchococcus RF-1

When nitrogen fixing cell cultures of Synechococcus RF-1 were subjected to an alternating lightdark regime (12 h:12 h), a cyclic decrease in the photosynthetic oxygen evolution potential was observed during the dark periods. This rhythm of net photosynthesis rate was maintained for at least two days after transition to continuous light. The decrease in net photosynthesis was accompanied by a stimulation of dark respiration. However, the magnitude of oxygen uptake was considerably smaller than the observed decrease in oxygen evolution. The photosynthetic activity of cells taken from the dark period was characterized by (i) a significantly lower quantum yield and (ii) a strong reduction in the light-saturated rate of photosynthesis. Growing the cultures on nitrate or under continuous light completely suppressed this rhythm. Protein synthesis was not necessary for the recovery of the light-saturated rate of photosynthesis during the light period. The cellular content of chlorophyll a and of phycobiliproteins did not vary between light and dark period, indicating that quantitative changes in the composition of the photosynthetic apparatus are not the basis for the observed oscillations. Regulatory modifications of the photosynthetic efficiency are proposed as an adaptation mechanism to adjust the intracellular oxygen concentration to the needs for nitrogenase activity.Abbreviation Chl chlorophyll