The effects of elevated [CO2] and water availability on growth and physiology of peach (Prunus persica) plants

ABSTRACT

Peach (Prunus persica L.) seedlings were germinated and grown for two growing seasons either in open top chambers (OTC) with ambient (350 μmol mol^-1) or elevated (700 μmol mol^-1) [CO₂], or in an outside control plot, all located inside a glasshouse. The seedlings were grown in 10 dm³ pots and were fertilised once a week following Ingestad principles in order to supply mineral nutrients at free access rates. In the second growing season, rapid onset of water stress was imposed on rapidly growing peach seedlings by withholding water for a four-week drying cycle. In elevated [CO₂], seedlings had a total dry mass which was 33% higher than that in ambient [CO₂]. This increase was largely a consequence of increased height growth. [CO₂] and irrigation treatments had only small effects on allocation, and there was no increase in root allocation with low water availability possibly as consequence of the high-nutrient regime. Specific leaf area was significantly reduced in elevated [CO₂], and probably resulted from increases in starch concentrations. Stomatal conductance (g _s) was not affected by elevated [CO₂] both in well-watered and water-stressed seedlings. The combination of increased assimilation rate (A) and unchanged g _s led to large increases in intrinsic water use efficiency in response to elevated [CO₂]. The A/C _i curves were used to derive the parameters describing photosynthetic capacity, A_max, J_max and V_cmax . These parameters were similar among [CO₂] treatments; thus, there was no downward acclimation of photosynthesis in elevated [CO₂]. Moreover, A_max, J_max and V_cmax scaled linearly with leaf N content per unit leaf area. This indicates that the whole-plant source-sink balance of peach seedlings was not disrupted by growth in elevated [CO₂], because root volume and nutrient supply were non-restricting. These values may be used in scaling up models to improve their ability to predict the magnitude of tree responses to climate change in the Mediterranean area.     

How is the relationship between the C4 cereal Sorghum bicolor and the C3 root hemi-parasites Striga hermonthica and Striga asiatica affected by elevated CO2?

The C₄ cereal Sorghum bicolor was grown under either ambient (350 μmol mol^?1) or elevated (700 μmol mol^?1) [CO₂] in either the presence or absence of the C₃ obligate root hemi-parasites Striga hermonthica or S. asiatica. Both uninfected and infected sorghum plants were taller and had greater biomass, photosynthetic rates, water-use efficiencies and leaf areas under elevated compared with ambient [CO₂]. There was no evidence of any downregula-tion of photosynthesis in sorghum grown at elevated [CO₂]. Biomass of infected sorghum was lower under both ambient and elevated [CO₂], and although infected plants were larger under elevated [CO₂] the relative impact of infection on host biomass was either the same (S. asiatica) or only slightly less (S. hermonthica) than under ambient [CO₂]. In contrast, biomass of S. hermonthica and S. asiatica per host was lower under elevated than ambient [CO₂], although rates of photosynthesis were higher at elevated [CO₂] and parasite stomatal conductance was not responsive to [CO₂]. Parasites emerged above-ground and flowered earlier under ambient compared with elevated [CO₂]. It appears that the mechanism(s) by which the parasites affect host growth is (are) relatively insensitive to increased atmospheric [CO₂], although the parasites themselves were adversely affected by growth at elevated [CO₂].     

Atmospheric carbon dioxide and fertilizer nitrogen effects on radiation interception by rice 1

In order to predict the potential impacts of global change, it is important to understand the impact of increasing global atmospheric [CO₂] on the growth and yield of crop plants. The objectives of this study were to determine the interaction of N fertilization rates and atmospheric [CO₂] on radiation interception and radiation-use efficiency of rice (Oryza sativa L. cv. IR72) grown under tropical field conditions. Rice plants were grown inside open top chambers in a lowland rice field at the International Rice Research Institute in the Philippines at ambient (about 350 μmol mol^-1) or elevated (about 600 μmol mol^-1 during the 1993 wet season and 700 μmol mol^-1 during the 1994 dry season) in combination with three levels of applied N (0, 50 or 100 kg N ha^-1 in the wet season; 0, 90 or 200 kg N ha-1 in the dry season). Light interception was not directly affected by [CO₂], but elevated [CO₂] indirectly increased light interception through increasing total absorbed N. Plant N requirement for radiation interception was similar for rice grown under ambient [CO₂] or elevated [CO₂] treatments. The conversion efficiency of intercepted radiation to dry matter, radiation-use efficiency (RUE), was about 35% greater at elevated [CO₂] than at ambient [CO₂]. The relationship between leaf N and RUE was curvilinear. At ambient [CO₂], RUE was fairly stable across levels of leaf N, but leaf N less than about 2.5% resulted in lower RUE for plants grown with elevated [CO₂] than for plant grown at ambient [CO₂]. Decreased leaf N with increased [CO₂], therefore decreased RUE of rice plants grown at elevated [CO₂]. When predicting responses of rice to elevated [CO₂], RUE should be adjusted with a decrease in leaf N. This revised version was published online in June 2006 with corrections to the Cover Date.     

The impact of elevated carbon dioxide on the growth and gas exchange of three C4 species differing in CO2 leak rates

Recent work has suggested that the photosynthetic rate of certain C₄ species can be stimulated by increasing CO₂ concentration, [CO₂], even under optimal water and nutrients. To determine the basis for the observed photosynthetic stimulation, we tested the hypothesis that the CO₂ leak rate from the bundle sheath would be directly related to any observed stimulation in single leaf photosynthesis at double the current [CO₂]. Three C₄ species that differed in the reported degree of bundle sheath leakiness to CO₂, Flaveria trinervia, Panicum miliaceum, and Panicum maximum, were grown for 31–48 days after sowing at a [CO₂] of 350 μl l^?1 (ambient) or 700 μl l^?1 (elevated). Assimilation as a function of increasing [CO₂] at high photosynthetic photon flux density (PPFD, 1 600 μmol m^?2 s^?1) indicated that leaf photosynthesis was not saturated under current ambient [CO₂] for any of the three C₄ species. Assimilation as a function of increasing PPFD also indicated that the response of leaf photosynthesis to elevated [CO₂] was light dependent for all three C₄ species. The stimulation of leaf photosynthesis at elevated [CO₂] was not associated with previously published values of CO₂ leak rates from the bundle sheath, changes in the ratio of activities of PEP-carboxylase to RuBP carboxylase/oxgenase, or any improvement in daytime leaf water potential for the species tested in this experiment. In spite of the simulation of leaf photosynthesis, a significant increase in growth at elevated [CO₂] was only observed for one species, F. trinervia. Results from this study indicate that leaf photosynthetic rates of certain C₄ species can respond directly to increased [CO₂] under optimal growth conditions, but that the stimulation of whole plant growth at elevated carbon dioxide cannot be predicted solely on the response of individual leaves.     

Temperature/light dependent development of selective resistance to photoinhibition of photosystem I

Exposure of winter rye leaves grown at 20°C and an irradiance of either 50 or 250 μmol m⁻² s⁻¹ to high light stress (1600 μmol m⁻² s⁻¹, 4 h) at 5°C resulted in photoinhibition of PSI measured in vivo as a 34% and 31% decrease in ΔA₈₂₀/A₈₂₀ (P700⁺). The same effect was registered in plants grown at 5°C and 50 μmol m⁻² s⁻¹. This was accompanied by a parallel degradation of the PsaA/PsaB heterodimer, increase of the intersystem e⁻ pool size as well as inhibition of PSII photochemistry measured as F_v/F_m. Surprisingly, plants acclimated to high light (800 μmol m⁻² s⁻¹) or to 5°C and moderate light (250 μmol m⁻² s⁻¹) were fully resistant to photoinhibition of PSI and did not exhibit any measurable changes at the level of PSI heterodimer abundance and intersystem e⁻ pool size, although PSII photochemistry was reduced to 66% and 64% respectively. Thus, we show for the first time that PSI, unlike PSII, becomes completely resistant to photoinhibition when plants are acclimated to either 20°C/800 μmol m⁻² s⁻¹ or 5°C/250 μmol m⁻² s⁻¹ as a response to growth at elevated excitation pressure. The role of temperature/light dependent acclimation in the induction of selective tolerance to PSI photoinactivation is discussed.     

Direct and acclimatory responses of stomatal conductance to elevated carbon dioxide in four herbaceous crop species in the field

In order to separate the net effect of growth at elevated [CO₂] on stomatal conductance (g_s) into direct and acclimatory responses, mid‐day values of g_s were measured for plants grown in field plots in open‐topped chambers at the current ambient [CO₂], which averaged 350 μmol mol^?1 in the daytime, and at ambient + 350 μmol mol^?1[CO₂] for winter wheat, winter barley, potato and sorghum. The acclimatory response was determined by comparing g_s measured at 700 μmol mol^?1[CO₂] for plants grown at the two [CO₂]. The direct effect of increasing [CO₂] from 350 to 700 μmol mol^?1 was determined for plants grown at the lower concentration. Photosynthetic rates were measured concurrently with g_s. For all species, growth at the higher [CO₂] significantly reduced g_s measured at 700 μmol mol^?1[CO₂]. The reduction in g_s caused by growth at the higher [CO₂] was larger for all species on days with low leaf to air water vapour pressure difference for a given temperature, which coincided with highest conductances and also the smallest direct effects of increased [CO₂] on conductance. For barley, there was no other evidence for stomatal acclimation, despite consistent down‐regulation of photosynthetic rate in plants grown at the higher [CO₂]. In wheat and potato, in addition to the vapour pressure difference interaction, the magnitude of stomatal acclimation varied directly in proportion to the magnitude of down‐regulation of photosynthetic rate through the season. In sorghum, g_s consistently exhibited acclimation, but there was no down‐regulation of photosynthetic rate. In none of the species except barley was the direct effect the larger component of the net reduction in g_s when averaged over measurement dates. The net effect of growth at elevated [CO₂] on mid‐day g_s resulted from unique combinations of direct and acclimatory responses in the various species.     

Interactive effects of nitrogen and phosphorus on the acclimation potential of foliage photosynthetic properties of cork oak,Quercus suber,to elevated atmospheric CO2 concentrations

Leaf gas-exchange and chemical composition were investigated in seedlings of Quercus suber L. grown for 21 months either at elevated (700 μmol mol^–1) or normal (350 μmol mol^–1) ambient atmospheric CO₂ concentrations, [CO₂], in a sandy nutrient-poor soil with either ‘high’ N (0.3 mol N m^–3 in the irrigation solution) or with ‘low’ N (0.05 mol N m^–3) and with a constant suboptimal concentration of the other macro- and micronutrients. Although elevated [CO₂] yielded the greatest total plant biomass in ‘high’ nitrogen treatment, it resulted in lower leaf nutrient concentrations in all cases, independent of the nutrient addition regime, and in greater nonstructural carbohydrate concentrations. By contrast, nitrogen treatment did not affect foliar N concentrations, but resulted in lower phosphorus concentrations, suggesting that under lower N, P use-efficiency in foliar biomass production was lower. Phosphorus deficiency was evident in all treatments, as photosynthesis became CO₂ insensitive at intercellular CO₂ concentrations larger than ≈ 300 μmol mol^–1, and net assimilation rates measured at an ambient [CO₂] of 350 μmol mol^–1 or at 700 μmol mol^–1 were not significantly different. Moreover, there was a positive correlation of foliar P with maximum Rubisco (Ribulose-1,5-bisphosphate carboxylase/oxygenase) carboxylase activity (V_cmax), which potentially limits photosynthesis at low [CO₂], and the capacities of photosynthetic electron transport (J_max) and phosphate utilization (P_max), which are potentially limiting at high [CO₂]. None of these potential limits was correlated with foliar nitrogen concentration, indicating that photosynthetic N use-efficiency was directly dependent on foliar P availability. Though the tendencies were towards lower capacities of potential limitations of photosynthesis in high [CO₂] grown specimens, the effects were statistically insignificant, because of (i) large within-treatment variability related to foliar P, and (ii) small decreases in P/N ratio with increasing [CO₂], resulting in balanced changes in other foliar compounds potentially limiting carbon acquisition. The results of the current study indicate that under P-deficiency, the down-regulation of excess biochemical capacities proceeds in a similar manner in leaves grown under normal and elevated [CO₂], and also that foliar P/N ratios for optimum photosynthesis are likely to increase with increasing growth CO₂ concentrations. Symbols: A, net assimilation rate (μmol m^–2 s^–1); A_max, light-saturated A (μmol m^–2 s^–1); α, initial quantum yield at saturating [CO₂] and for an incident Q (mol mol^–1); [CO₂], atmospheric CO₂ concentration (μmol mol^–1); C_i, intercellular CO₂ concentration (μmol mol^–1); C_a, CO₂ concentration in the gas-exchange cuvette (μmol mol^–1); F_B, fraction of leaf N in ‘photoenergetics’; F_L, fraction of leaf N in light harvesting; F_R, fraction of leaf N in Rubisco; Γ*, CO₂ compensation concentration in the absence of R_d (μmol mol^–1); J_max*, capacity for photosynthetic electron transport; J_mc, capacity for photosynthetic electron transport per unit cytochrome f (mol e^–[mol cyt f]^–1 s^–1); K_c, Michaelis-Menten constant for carboxylation (μmol mol^–1); K_o, Michaelis-Menten constant for oxygenation (mmol mol^–1); M_A, leaf dry mass per area (g m^–2); O, intercellular oxygen concentration (mmol mol^–1); [P_i], concentration of inorganic phosphate (mM); P_max*, capacity for phosphate utilization; Q, photosynthetically active quantum flux density (μmol m^–2 s^–1); R_d*, day respiration (CO₂ evolution from nonphotorespiratory processes continuing in the light); Rubisco, ribulose-1,5-bisphosphate carboxylase/oxygenase; RUBP, ribulose-1,5-bisphosphate; T_l, leaf temperature (°C); U_TPU*, rate of triose phosphate utilization; V_cmax*, maximum Rubisco carboxylase activity; V_cr, specific activity of Rubisco (μmol CO₂[g Rubisco]^–1 s^–1] *given in either μmol m^–2 s^–1 or in μmol g^–1 s^–1 as described in the text.     

Effects of Elevated [CO2] and Low Soil Moisture on the Physiological Responses of Mountain Maple (Acer spicatum L.) Seedlings to Light

Global climate change is expected to affect how plants respond to their physical and biological environments. In this study, we examined the effects of elevated CO₂ ([CO₂]) and low soil moisture on the physiological responses of mountain maple (Acer spicatum L.) seedlings to light availability. The seedlings were grown at ambient (392 µmol mol⁻¹) and elevated (784 µmol mol⁻¹) [CO₂], low and high soil moisture (M) regimes, at high light (100%) and low light (30%) in the greenhouse for one growing season. We measured net photosynthesis (A), stomatal conductance (g _s), instantaneous water use efficiency (IWUE), maximum rate of carboxylation (V _cmax), rate of photosynthetic electron transport (J), triose phosphate utilization (TPU)), leaf respiration (R _d), light compensation point (LCP) and mid-day shoot water potential (Ψ_x). A and g _s did not show significant responses to light treatment in seedlings grown at low soil moisture treatment, but the high light significantly decreased the C _i/C _a in those seedlings. IWUE was significantly higher in the elevated compared with the ambient [CO₂], and the effect was greater at high than the low light treatment. LCP did not respond to the soil moisture treatments when seedlings were grown in high light under both [CO₂]. The low soil moisture significantly reduced Ψ_x but had no significant effect on the responses of other physiological traits to light or [CO₂]. These results suggest that as the atmospheric [CO₂] rises, the physiological performance of mountain maple seedlings in high light environments may be enhanced, particularly when soil moisture conditions are favourable.     

Net ecosystem CO2 exchange in Mojave Desert shrublands during the eighth year of exposure to elevated CO2

Arid ecosystems, which occupy about 35% of the Earth's terrestrial surface area, are believed to be among the most responsive to elevated [CO₂]. Net ecosystem CO₂ exchange (NEE) was measured in the eighth year of CO₂ enrichment at the Nevada Desert Free‐Air CO₂ Enrichment (FACE) Facility between the months of December 2003–December 2004. On most dates mean daily NEE (24 h) (μmol CO₂ m^?2 s^?1) of ecosystems exposed to elevated atmospheric CO₂ were similar to those maintained at current ambient CO₂ levels. However, on sampling dates following rains, mean daily NEEs of ecosystems exposed to elevated [CO₂] averaged 23 to 56% lower than mean daily NEEs of ecosystems maintained at ambient [CO₂]. Mean daily NEE varied seasonally across both CO₂ treatments, increasing from about 0.1 μmol CO₂ m^?2 s^?1 in December to a maximum of 0.5–0.6 μmol CO₂ m^?2 s^?1 in early spring. Maximum NEE in ecosystems exposed to elevated CO₂ occurred 1 month earlier than it did in ecosystems exposed to ambient CO₂, with declines in both treatments to lowest seasonal levels by early October (0.09±0.03 μmol CO₂ m^?2 s^?1), but then increasing to near peak levels in late October (0.36±0.08 μmol CO₂ m^?2 s^?1), November (0.28±0.03 μmol CO₂ m^?2 s^?1), and December (0.54±0.06 μmol CO₂ m^?2 s^?1). Seasonal patterns of mean daily NEE primarily resulted from larger seasonal fluctuations in rates of daytime net ecosystem CO₂ uptake which were closely tied to plant community phenology and precipitation. Photosynthesis in the autotrophic crust community (lichens, mosses, and free‐living cyanobacteria) following rains were probably responsible for the high NEEs observed in January, February, and late October 2004 when vascular plant photosynthesis was low. Both CO₂ treatments were net CO₂ sinks in 2004, but exposure to elevated CO₂ reduced CO₂ sink strength by 30% (positive net ecosystem productivity=127±17 g C m^?2 yr^?1 ambient CO₂ and 90±11 g C m^?2 yr^?1 elevated CO₂, P=0.011). This level of net C uptake rivals or exceeds levels observed in some forested and grassland ecosystems. Thus, the decrease in C sequestration seen in our study under elevated CO₂– along with the extensive coverage of arid and semi‐arid ecosystems globally – points to a significant drop in global C sequestration potential in the next several decades because of responses of heretofore overlooked dryland ecosystems.     

The effects of elevated atmospheric CO2 on the amount and depth distribution of plant water uptake in a California annual grassland

Soil moisture profiles can affect species composition and ecosystem processes, but the effects of increased concentrations of atmospheric carbon dioxide ([CO₂]) on the vertical distribution of plant water uptake have not been studied. Because plant species composition affects soil moisture profiles, and is likely to shift under elevated [CO₂], it is also important to test whether the indirect effects of [CO₂] on soil water content may depend on species composition. We examined the effects of elevated [CO₂] and species composition on soil moisture profiles in an annual grassland of California. We grew monocultures and a mixture of Avena barbata and Hemizonia congesta– the dominant species of two phenological groups – in microcosms exposed to ambient (～370 μmol mol^?1) and elevated (～700 μmol mol^?1) [CO₂]. Both species increased intrinsic and yield‐based water use efficiency under elevated [CO₂], but soil moisture increased only in communities with A. barbata, the dominant early‐season annual grass. In A. barbata monocultures, the [CO₂] treatment did not affect the depth distribution of soil water loss. In contrast to communities with A. barbata, monocultures of H. congesta, a late‐season annual forb, did not conserve water under elevated [CO₂], reflecting the increased growth of these plants. In late spring, elevated [CO₂] also increased the efficiency of deep roots in H. congesta monocultures. Under ambient [CO₂], roots below 60 cm accounted for 22% of total root biomass and were associated with 9% of total water loss, whereas in elevated [CO₂], 16% of total belowground biomass was associated with 34% of total water loss. Both soil moisture and isotope data showed that H. congesta monocultures grown under elevated [CO₂] began extracting water from deep soils 2 weeks earlier than plants in ambient [CO₂].     

Photosynthetic performance of vegetative and reproductive structures of green hellebore (<Emphasis Type="Italic">Helleborus viridis</Emphasis> L. agg.)

Photosynthetic irradiance response of vegetative and reproductive structures of the green-flowered deciduous perennial green hellebore was studied by the comparative use of chlorophyll (Chl) fluorescence techniques and gas exchange measurements. All the Chl-containing organs (leaves, sepals, stalks, and fruits) examined were photosynthetically active showing high intrinsic efficiencies of photosystem 2 (F_v/F_m: 0.75–0.79) after dark adaptation. Even in the smaller fertile and sterile parts of the flower (nectaries and anthers) a remarkable photosynthetic competence was detected. With increasing photon flux densities (PFD) electron transport rates, actual quantum yields, and photochemical quenching coefficients of the main photosynthetic organs decreased in the order: leaf>sepal>fruit>stalk. At moderate to high PFDs the sepals achieved maximum electron transport rates corresponding to about 80 % of concomitant mature leaves. In contrast, maximum net photosynthetic rate of the sepals [2.3 mol(CO₂) m^–2 s^–1] were less than one fourth of the leaves [10.6 mol(CO₂) m^–2 s^–1]. This difference is explained by a 70–80 % lower stomatal density of sepals in comparison to leaves. As the basal leaves emerge late during fruit development, the photosynthetically active sepals are a major source of assimilates, contributing more than 60 % of whole-plant CO₂ gain in early spring. The ripening dehiscent fruits are characterized by an effective internal re-fixation of the respirational carbon loss and thus additionally improve the overall carbon budget.     

Avocado shoot culture, plantlet development and net CO2 assimilation in an ambient and CO2 enhanced environment

Summary The proliferation and survival of avocado nodal cultures of juvenile origin were affected by the form and concentration of nitrogen. Optimum growth was achieved on modified Murashige and Skoog medium containing 67% KNO₃ and 33% NH₄NO₃ with total N of 40 mM supplemented with 100 mg l⁻¹ myo-inositol, 1 mg l⁻¹ thiamine HCl, 30 g l⁻¹ sucrose, and 4.44 μM BA with a 16-h photoperiod (120–150 μmol m⁻² s⁻¹). Proliferating shoots and plantlets were photosynthetically active. Better shoot growth and accumulation of higher biomass occurred in a CO₂-enriched environment than under ambient CO₂ conditions. CO₂ assimilation efficiency, however, was higher under the latter conditions than in a CO₂-enhanced environment, e.g., 31±7 and 17±2 μmol CO₂ m⁻² s⁻¹, respectively. The net CO₂ assimilation rates of in vitro grown plantlets were comparable to those of seedlings ex vitro.     

The impact of recent increases in atmospheric CO2 on biomass production and vegetative retention of Cheatgrass (Bromus tectorum): implications for fire disturbance

Cheatgrass (Bromus tectorum) is a recognized, invasive annual weed of the western United States that reduces fire return times from decades to less than 5 years. To determine the interaction between rising carbon dioxide concentration ([CO₂]) and fuel load, we characterized potential changes in biomass accumulation, C : N ratio and digestibility of three cheatgrass populations from different elevations to recent and near‐term projections in atmospheric [CO₂]. The experimental CO₂ values (270, 320, 370, 420 μmol mol^?1) corresponded roughly to the CO₂ concentrations that existed at the beginning of the 19th century, that during the 1960s, the current [CO₂], and the near‐term [CO₂] projection for 2020, respectively. From 25 until 87 days after sowing (DAS), aboveground biomass for these different populations increased 1.5–2.7 g per plant for every 10 μmol mol^?1 increase above the 270 μmol mol^?1 preindustrial baseline. CO₂ sensitivity among populations varied with elevational origin with populations from the lowest elevation showing the greatest productivity. Among all populations, the undigestible portion of aboveground plant material (acid detergent fiber ADF, mostly cellulose and lignin) increased with increasing [CO₂]. In addition, the ratio of C : N increased with leaf age, with [CO₂] and was highest for the lower elevational population. These CO₂‐induced qualitative changes could, in turn, result in potential decreases in herbivory and decomposition with subsequent effects on the aboveground retention of cheatgrass biomass. Overall, these data suggest that increasing atmospheric [CO₂] above preambient levels may have contributed significantly to cheatgrass productivity and fuel load with subsequent effects on fire frequency and intensity.     

Stomatal acclimation to increased CO2 concentration in a Florida scrub oak species Quercus myrtifolia Willd

Native scrub‐oak communities in Florida were exposed for three seasons in open top chambers to present atmospheric [CO₂] (approx. 350 μmol mol^?1) and to high [CO₂] (increased by 350 μmol mol^?1). Stomatal and photosynthetic acclimation to high [CO₂] of the dominant species Quercus myrtifolia was examined by leaf gas exchange of excised shoots. Stomatal conductance (g_s) was approximately 40% lower in the high‐ compared to low‐[CO₂]‐grown plants when measured at their respective growth concentrations. Reciprocal measurements of g_s in both high‐ and low‐[CO₂]‐grown plants showed that there was negative acclimation in the high‐[CO₂]‐grown plants (9–16% reduction in g_s when measured at 700 μmol mol^?1), but these were small compared to those for net CO₂ assimilation rate (A, 21–36%). Stomatal acclimation was more clearly evident in the curve of stomatal response to intercellular [CO₂] (c_i) which showed a reduction in stomatal sensitivity at low c_i in the high‐[CO₂]‐grown plants. Stomatal density showed no change in response to growth in high growth [CO₂]. Long‐term stomatal and photosynthetic acclimation to growth in high [CO₂] did not markedly change the 2·5‐ to 3‐fold increase in gas‐exchange‐derived water use efficiency caused by high [CO₂].     

Photosynthetic gas exchange response of poplars to steady-state and dynamic light environments

The steady-state and dynamic photosynthetic response of two poplar species (Populus tremuloides and P. fremontii) to variations in photon flux density (PFD) were observed with a field portable gas exchange system. These poplars were shown to be very shade intolerant with high light saturation (800 to 1300 mol photons m^–2 s^–1) and light compensation (70 to 100 mol m^–2 s^–1) points. Understory poplar leaves showed no physiological acclimation to understory light environments. These plants become photosynthetically induced quickly (10 min). Activation of Rubisco was the primary limitation for induction, with stomatal opening playing only a minor role. Leaves maintained high stomatal conductances and stomata were unresponsive to variations in PFD. Leaves were very efficient at utilizing rapidly fluctuating light environments similar to those naturally occurring in canopies. Post-illumination CO₂ fixation contributed proportionally more to the carbon gain of leaves during short frequent lightflecks than longer less frequent ones. The benefits of a more dynamic understory light environment for the carbon economy of these species are discussed.     

Photosynthetic response of Prorocentrum mariae-lebouriae (Dinophyceae) to different spectral qualities,irradiances, and temperatures

Photosynthetic productivity (P_s) of the estuarine dinoflagellate Prorocentrum mariae-lebouriae (Parke and Ballantine) comb. nov., was measured with an open differential infra-red gas analysis system especially designed to measure CO₂ uptake at a constant CO₂ concentration. P_s was determined in six different fluorescent lamp spectral qualities (SQ) (daylight, blue, green, orange, orange-red and red) with bandwiths ranging from 50 to 75 nm and at photon flux densities (PFD) from 1.7 to 170 mol of quanta s^–1 m^–2 to characterize the spectral response of daylight SQ grown P. mariae-lebouriae cultures. P_s was significantly higher for blue irradiation than for any other SQ. Compared to blue (100%) the following mean values were found: daylight 88%, green 79%, orange 29%, orange-red 56%, and red 87%. Differences were greatest at low PFD. Most measurements were performed at 20°C, but P_s was found to vary as a direct function of the culture temperature. A 10°C increase in temperature caused a 50% increase in P_s from 10° to 30°C with saturating PFD. Since the analytical system measured very small CO₂ differentials, down to 0.5 l l^–1, we were able to detect small and fast CO₂ transients at the beginning and end of an irradiation. These transients, known as CO₂-burst and CO₂-gulp, increased in magnitude with increased PFD.     

Growth response of cotton to CO2 enrichment in differing light environments

Experiments were conducted to examine the growth responses of cotton (Gossypium hirsutum L. cv. Coker 315) to CO₂ enrichment under different light regimes. Plants were exposed to 350 or 700 μl l^?1 CO₂ and six light treatments differing in photosynthetic period length (8 or 16 h) and in photosynthetic photon flux density (PPFD) for 32 days of vegetative growth. Higher PPFD (1 100 μmol m^?2 s^?1) was provided by a combination of high intensity discharge and incandescent lamps (HID), and lower PPFD (550 μmol m^?2 s^?1) was provided by fluorescent and incandescent lamps (F) or HID and incandescent lamps with shade cloth (HID_s). Growth was generally much slower with the 8-h photosynthetic periods, but the growth stimulation by CO₂ enrichment was larger than with 16-h photosynthetic periods. After 28 to 32 days of treatment, the growth enhancement with CO₂ enrichment was 152 and 78% for 8- and 16-h photosynthetic periods, respectively, under HID; 100 and 77% in F, and 77 and 56% in HID_s. The higher PPFD of HID positively influenced the CO₂ effect only at the slower growth rate in the 8-h light period. The stimulation of leaf area expansion by CO₂ enrichment was also greater with the 8-h photosynthetic period for all light sources. These results, and others on net assimilation rate, shoot to root dry weight ratios and specific leaf weights, suggest that the growth response to CO₂ enrichment with the longer photosynthetic period was depressed by limiting factors, perhaps nutritional, in the growth environment. The results also show that extensive variability in CO₂ response can occur under light intensities which are often used in growth chamber experiments.     

Influences of light and UV-B on growth and sporulation of the green alga Ulva pertusa Kjellman

The cosmopolitan presence of Ulva spp. is partly due to its great reproductive ability, but relatively little information is available for the radiation conditions triggering reproduction. In the present study, we investigated the effect of photon irradiance, photoperiod, and spectral qualities of light on growth and reproduction of Ulva pertusa.During 8-day culture of discs cut from marginal parts of the thallus of U. pertusa, the size of the thallus discs was greatest at 10 μmol m⁻² s⁻¹, while saturation of reproduction occurred at 30 μmol m⁻² s⁻¹. The minimum photon irradiance allowing growth and reproduction was 5 and 10 μmol m⁻² s⁻¹, respectively. Rapid increases in the size and subsequent initiation of sporulation were observed in samples transferred to saturating irradiance from 5 μmol m⁻² s⁻¹ or darkness for 9 days. When exposed to different photoperiods (8:16-, 12:12-, 16:8-h LD and continuous light regimes) combined with different photon irradiances (10 and 100 μmol m⁻² s⁻¹), U. pertusa thallus showed that the thallus size attained at the low irradiance was similar in daylengths longer than 12 h per day, while the surface area increased in parallel with increasing light duration at the high irradiance. The degree of sporulation at 10 μmol m⁻² s⁻¹ varied, ranging from no sporulation in 8:16-h LD to 80% in 16:8-h LD and continuous light. On the other hand, there was no remarkable difference in the degree of sporulation between the photoperiods except for slightly smaller percentage sporulation in 8:16-h LD at 100 μmol m⁻² s⁻¹.At 5 μmol m⁻² s⁻¹, the growth of U. pertusa was markedly lower in green than in blue or red light, but there was no sporulation in any spectral quality. The degree of sporulation at 20 μmol m⁻² s⁻¹ was almost twice as much in blue or red as in green light.The size of plants irradiated with 1.0 W m⁻² of UV-B for 20-40 min increased by 18-21% relative to control, whereas higher UV irradiance caused inhibition of growth. There was a significantly lower incidence of sporulation in UV-B-irradiated plants with the degree of reduction being greater in those exposed to higher UV doses. The total biologically effective UV-B dose for 50% inhibition of sporulation was 0.085 Dose_eff kJ m⁻². The time required to achieve 50% inhibition would be longer than 13 h at depths below 1 m in Ahnin coastal waters. The vertical attenuation coefficient of PAR (λ=400-700 nm) and UV-B (λ=300-320 nm) in April 1998 at Ahnin on the eastern coast of Korea was 0.21 m⁻¹ for K_PAR and 0.54 m⁻¹ for K_UV-B. A large reduction of light quantity and rapid disappearance of blue wavelength occurred by shading from overlying thalli.Percentage inhibition of sporulation was only 14-18% at 150-200 μmol m⁻² s⁻¹ compared with 70% at 10 μmol m⁻² s⁻¹, when plants were incubated under different irradiances of PAR immediately after UV-B exposures.These different photoadaptive strategies for sporulation may in part account for the great ecological success of U. pertusa.     

GROWTH,PHOTOSYNTHESIS AND MAINTENANCE METABOLIC COST IN THE DIATOM PHAEODACTYLUM TRICORNUTUM AT VERY LOW LIGHT LEVELS 1

The compensation point for growth of Phaeodactylum tricornutum Bohlin is less than 1 μmol. m^?2s^?1. Growth at low PFDs (<3.5 μmol. m^?2.s^?1) does not appear to reduce the maximum quantum efficiency of photosynthesis (ø_m) or to greatly inhibit the potential for light-saturated, carbon-specific photosynthesis (P_m^c). The value for ø_m in P. tricornutum is 0.10–0.12 mol O₂-mol photon^?1, independent of acclimation PFD between 0.75 and 200 μmol.m^?2.s^?1 in nutrient-sufficient cultures. P_m^c in cells of P. tricornutum acclimated to PFDs <3.5 μmol m^?2?s^?1 is approximately 50% of the highest value obtained in nutrient-sufficient cultures acclimated to growth-rate-saturating PFDs. In addition, growth at low PFDs does not severely restrict the ability of cells to respond to an increase in light level. Cultures acclimated to growth at lees than 1% of the light-saturated growth rate respond rapidly to a shift-up in PFD after a short initial lag period and achieve exponential growth rates of 1.0 d^?1 (65% of the light- and nutrient-saturated maximum growth rate) at both 40 and 200 μmol.m^?2.s^?1     

Effects of growth-light quantity,growth-light quality and CO2 concentration on Rubisco deactivation during low PFD or darkness

The effects of CO₂ concentration and the effects of growth-light conditions on Ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco) deactivation were examined for Spinacea oleracea (spinach). Rubisco deactivation kinetics and the degree that Rubisco activation limited the rise in photosynthesis following an increase in photon flux density (PFD) were determined from gas-exchange time courses. There were no significant differences in the apparent relaxation time for Rubisco deactivation among leaves exposed to high or low CO₂ (50 or 1000 mol mol^-1) and low PFD (170 mol m^-2 s^-1) or darkness. However, when PFD was increased to 1700 mol m^-2 s^-1 following a period of low PFD or darkness, leaves exposed to low CO₂ × low PFD showed a lower contribution to the photosynthetic induction process by the activation of Rubisco than leaves exposed to the other treatments. For the growth-light experiments, spinach was grown under high PFD × high red:far-red ratio (R:FR), low PFD × high R:FR, or low PFD × low R:FR light environments. Leaves that matured under the low PFD × low R:FR treatment showed a lower percent change in photosynthesis due to Rubisco activation than leaves exposed to the other growth-light treatments. However, there were no significant differences among the growth-light treatments in the maximum contribution of Rubisco activation to the induction response or in the apparent relaxation time for Rubisco deactivation during shade events.