Photosynthesis and respiration in Alocasia macrorrhiza following transfers to high and low light

Summary Photosynthetic capacities and respiration rates of Alocasia macrorrhiza leaves were measured for 4 weeks following reciprocal transfers between high (20% of full sun) and low (1% of full sun) light environments. Photosynthetic capacities and respiration rates of mature, high-light leaves were 1.7 and 4.5 times those of low-light leaves, respectively. Following transfer, respiration rates adjusted within 1 week to those characteristic of plants grown in the new environment. By contrast, photosynthetic capacities either did not adjust or changed only slowly following transfer. Most of the difference in respiration between high- and low-light leaves was related to the carbohydrate status as determined by the daily PFD and little was directly related to the maintenance costs of the photosynthetic apparatus. Leaf construction cost was directly proportional to maximum photosynthetic capacity. Consequently, although daily carbon gain per unit leaf area was the same for low-light and high to low-light transferred plants within a week after transfer, the carbon return per unit of carbon investment in the leaves remained lower in the high to low transfer plants throughout the 4 week measurement period. Conversely, in high-light, the low leaf construction cost of the low to high-light transferred plants resulted in carbon gain per unit investment just as high as that of the high-light plants.     

Arbuscular Mycorrhizal Symbiosis with Arundo donax Decreases Root Respiration and Increases Both Photosynthesis and Plant Biomass Accumulation

The effect of arbuscular mycorrhiza (AM) symbiosis on plant growth is associated with the balance between costs and benefits. A feedback regulation loop has been described in which the higher carbohydrate cost to plants for AM symbiosis is compensated by increases in their photosynthetic rates. Nevertheless, plant carbon balance depends both on photosynthetic carbon uptake and respiratory carbon consumption. The hypothesis behind this research was that the role of respiration in plant growth under AM symbiosis may be as important as that of photosynthesis. This hypothesis was tested in Arundo donax L. plantlets inoculated with Rhizophagus irregularis and Funneliformis mosseae. We tested the effects of AM inoculation on both photosynthetic capacity and in vivo leaf and root respiration. Additionally, analyses of the primary metabolism and ion content were performed in both leaves and roots. AM inoculation increased photosynthesis through increased CO₂ diffusion and electron transport in the chloroplast. Moreover, respiration decreased only in AM roots via the cytochrome oxidase pathway (COP) as measured by the oxygen isotope technique. This decline in the COP can be related to the reduced respiratory metabolism and substrates (sugars and tricarboxylic acid cycle intermediates) observed in roots.     

Respiration and photosynthesis of bladders and leaves of aquatic utricularia species

In aquatic species of carnivorous utricularia, about 10 - 50 % of the total biomass consists of bladders. Utricularia bladders are physiologically very active organs though their chlorophyll content may greatly be reduced. To specify energetic costs of carnivory, respiration (RD) and net photosynthetic rate (PN) were compared in bladders and leaves or shoot segments of six aquatic utricularia species with differentiated (U. ochroleuca, U. intermedia, U. floridana) or non-differentiated shoots (U. vulgaris, U. australis, U. bremii) under optimum conditions (20 degrees C, [CO (2)] 0.20 mM, 400 micromol m (-2) s (-1) PAR). RD of bladders of six utricularia species (5.1 - 8.6 mmol kg (-1)(FW) h (-1)) was 75 - 200 % greater, than that in leaves in carnivorous or photosynthetic shoots (1.7 - 6.1 mmol kg (-1)(FW) h (-1)). Within individual species, this difference was statistically significant at P < 0.002 - 0.01. However, PN in photosynthetic leaves/shoots (40 - 117 mmol kg (-1)(FW) h (-1)) exceeded that in bladders (5.2 - 14.7 mmol kg (-1)(FW) h (-1)) 7 - 10 times. RD of empty bladders of U. ochroleuca was exactly the same as that in bladders containing prey. Though utricularia bladders are essential for uptake of growth limiting mineral nutrients N and P from prey as the main benefit of carnivory, the current results support previous work showing that bladder function requires greater metabolic (maintenance) cost and very low photosynthetic efficiency (great RD : PN ratio).     

Photosynthetically versatile thin shade leaves: A paradox of irradiance-response curves

Thick sun leaves have a larger construction cost per unit leaf area than thin shade leaves. To re-evaluate the adaptive roles of sun and shade leaves, we compared the photosynthetic benefits relative to the construction cost of the leaves. We drew photosynthetically active radiation (PAR)-response curves using the leaf-mass-based photosynthetic rate to reflect the cost. The dark respiration rates of the sun and shade leaves of mulberry (Morus bombycis Koidzumi) seedlings did not differ significantly. At irradiances below 250 μmol m⁻² s⁻¹, the shade leaves tended to have a significantly larger net photosynthetic rate (P _N) than the sun leaves. At irradiances above 250 μmol m⁻² s⁻¹, the P _N did not differ significantly. The curves indicate that plants with thin shade leaves have a larger daily CO₂ assimilation rate per construction cost than those with thick sun leaves, even in an open habitat. These results are consistently explained by a simple model of PAR extinction in a leaf. We must target factors other than the effective assimilation when we consider the adaptive roles of thick sun leaves.     

The influence of water stress preconditioning on dark respiration

The respiration rate of individual leaves of cotton (Gossypium hirsutum L. cv. Stoneville 213), beans (Phaseolus vulgaris L. cv. Bush Blue Lake), and sorghum (Sorghum vulgare Pers.) which had been fully expanded prior to a series of severe water stresses was compared with those of unstressed leaves of similar age. Measurements were made over a range of leaf temperatures. The respiration rate per unit area of the leaves of all rewatered plants were significantly lower than those of the plants which had not undergone water stress. During the stress periods, the leaves of all species suffered dry matter loss. The respiration rates per unit dry matter for cotton and beans were the same for the plants which had undergone stress as they were for the plants which had not undergone stress, thus for these two C3 plants the decrease in dark respiration due to water stress may be explained entirely by the loss of dry matter. Respiration rates of the water stressed sorghum leaves expressed on a per unit weight basis were significantly lower than those which had not undergone water stress preconditioning. The lower respiration rates of the stressed leaves when expressed on both a per unit area basis and a per unit weight basis for the C4 species indicate that water stress adaptation of C4 plants may include alterations in the respiratory mechanism or on the amount of residual respirable substrate. The light compensation points of all the species were not altered by the water stress preconditioning. This indicates that the mechanisms controlling the net photosynthetic exchange per unit leaf area underwent adaptations as a result of repeated water stress which decreased its efficiency.     

Carbon dioxide exchange rates in soybeans during podfilling as a function of potassium supply

Photosynthetic and dark respiration rates of single leaflets and whole plant canopies were measured during podfilling of soybean plants that were grown under low and high K regimes. Dark respiration rates of detached seed from these plants were also determined during the latter part of seed development. The study was carried out to test the hypothesis that low oil/protein ratios of seed from K-deficient plants resulted from the reduction in carbon availability within the plant, as a result of lower carbon assimilation rates and higher rates of respiratory carbon loss. Photosynthetic rates of upper canopy leaflets during early podfilling were depressed under K deficiency but this effect did not occur with whole plant canopies. In fact, towards the latter part of the podfilling period canopy photosynthetic rates were higher in K-deficient plants as nitrogen was exported earlier from the leaves in high-K plants, resulting in earlier leaf senescence in these plants. The level of K supply had no consistent effect on dark respiration rates of single leaflets or plant canopies, and had no effect on CO₂ evolution rates from detached, developing seed. The findings do not substantiate the hypothesis that reduced photosynthetic efficiency or enhanced respiratory carbon loss are responsible for lower oil/protein ratios in seed from K-deficient soybean plants.     

The impact of two gall-forming arthropods on the photosynthetic rates of their hosts

The impact of herbivores on host plant photosynthetic rates can range from negative to positive. While defoliation by chewing herbivores can result in increases in photosynthesis followed by compensatory growth, other herbivore guilds, such as mesophyll feeders which damage photosynthetic leaf tissues, almost always reduce photosynthetic rates. The impact of galling herbivores on host photosynthesis has rarely been examined, even though the limited tissue disruption and the strong metabolic sinks induced by gall-forming herbivores could potentially stimulate photosynthetic rates. I examined the hypothesis that gall-inducing herbivores could stimulate photosynthesis in neighboring leaves in response to increased sink-demand by the gall. To address this hypothesis, I measured photosynthetic rates of galled leaves or leaflets, neighboring ungalled leaves or leaflets, and ungalled leaves or leaflets on ungalled shoots on naturally growing Prunus serotina (wild cherry) and Rhus glabra (smooth sumac). The leaves of wild cherry were galled by an eriophyid mite, Phytoptus cerasicrumena; the leaves of smooth sumac by an aphid, Melaphis rhois. I found that both species reduced the photosynthetic rates of the leaves or leaflets they galled from 24 to 52% compared to ungalled leaves in ungalled areas of the plants. Contrary to my hypothesis, mite galls on wild cherry reduced photosynthesis of neighboring ungalled leaves within the same shoot by 24% compared to ungalled leaves on gall-free shoots. Aphid galls on sumac leaflets did not significantly alter the photosynthetic rates of neighboring leaflets relative to ungalled leaves on ungalled shoots. Although gall-formers would appear to have the potential to stimulate photosynthesis in the same manner as defoliating herbivores, i.e., by increasing sink demand relative to source supply, I found only negative impacts on photosynthesis. I suggest that sink competition for nutrients between developing leaves and growing gall tissue may account for the negative impacts of sink-inducing gallers on photosynthesis. Received: 17 October 1997 / Accepted: 2 February 1998     

Effects of leaf and sap feeding insects on photosynthetic rates of goldenrod

Summary Herbivory can alter the balance between sources and sinks within a plant, and changes in the source-sink ratio often lead to changes in plant photosynthetic rates. We investigated how feeding by three insect herbivores affected photosynthetic rates and growth of goldenrod (Solidago altissima). One, a phloem-sap feeding aphid (Uroleucon caligatum), creates an additional sink, and the other two, a leaf-chewing beetle (Trirhabda sp.) and a xylem-sap feeding spittlebug (Philaenus spumarius) both reduce source supply by decreasing leaf area. Plants were grown outside in large pots and insects were placed on them at predetermined densities, with undamaged plants included as controls. All insects were removed after a 12-day feeding period. We measured photosynthetic rates both of damaged leaves and of undamaged leaves that were produced after insect removal. Photosynthetic rates per unit area of damaged leaves were reduced by spittlebug feeding, but not by beetle or aphid feeding. Conductance of spittlebugdamaged leaves did not differ from controls, but internal carbon dioxide concentrations were increased. These results indicate that spittlebug feeding does not cause stomatal closure, but impairs fixation within the leaf. Effects of spittlebug feeding on photosynthetic rates persisted after the insects were removed from the plants. Photosynthetic rates per unit area of leaves produced after insect removal on spittlegug-damaged plants were lower than control levels, even though the measurements were taken 12 days after insect removal. The measurement leaf on spittlebugdamaged plants was reduced in area by 27% relative to the controls, but specific leaf area (leaf area/leaf weight) was increased by 18%. Because of the shift in specific leaf area, photosynthetic rates were also examined per unit leaf weight, and when this was done there were no significant differences between control and spittlebug-damaged plants. Beetle and aphid feeding had no effects on the photosynthetic rate of the leaves produced after insect removal. Plant relative growth rates (in terms of height) were reduced by spittlebugs during the period that the insects were feeding on the plants. Relative growth rates of spittlebug-damaged plants were increased above control levels after insect removal, but these plants were still shorter than controls 17 days after insect removal. Beetles and aphids did not affect plant relative growth rates or plant height. Feeding by both spittlebugs and beetles reduced leaf area, and the effect of the spittlebug was more severe than that of the beetle. These results show that effects of herbivory on photosynthetic rates cannot be predicted simply by considering changes in the source-sink ratio, and that spittlebug feeding is more damaging to the host plant than beetle or aphid feeding.     

Photosynthesis in relation to leaf characteristics of cotton from controlled and field environments

In situ and light-saturated net photosynthetic rates per unit leaf area were greater in cotton (Gossypium hirsutum L.) plants grown in pots in the field than in similar plants from a phytotron growth chamber. Light-saturated stomatal resistances did not differ in leaves of similar age and exposure on field and chamber plants; lower photosynthetic rates in chamber leaves were associated with greater mesophyll resistance. Differences in net photosynthetic rates were related to differences in leaf thickness. When the photosynthetic rates were expressed per unit of mesophyll volume or per unit chlorophyll differences between field and chamber plants were much less than when rates were expressed per unit leaf area. Characterization of the chloroplast lamellar proteins showed that the field leaves had smaller photosynthetic units than the chamber leaves. Since the field leaves also contained more chlorophyll per unit area, this resulted in a much larger number of photosynthetic units per unit area in the field leaves.     

Contrasting oxygen dynamics in the freshwater isoetid Lobelia dortmanna and the marine seagrass Zostera marina

BACKGROUND: and Aims Submerged plants possess well-developed aerenchyma facilitating intra-plant gas-phase diffusion of O2 to below-ground tissues, which are usually buried in anoxic sediments. However, aquatic habitats differ in terms of O2 fluctuations in the water column and in O2 consumption of the sediment, and aquatic plants differ in aerenchymal volume and resistance to O2 diffusion through the plant and across leaf and root surfaces. The hypothesis that the freshwater isoetid Lobelia dortmanna and the marine seagrass Zostera marina should display pronounced contrasts in intra-plant O2 dynamics because of differences in morphology/anatomy, physiology and growth habitat was tested. METHODS: In order to determine the O2 dynamics and relate this to the anatomy and morphology of the two species, O2 microelectrodes were inserted in the aerenchyma of leaves and roots, the sediment pore-water, and the water column in the field. Manipulation of water column O2 in the laboratory was also carried out. KEY RESULTS: It was found that intra-plant transport of O2 between leaf and root tips takes place more readily in L. dortmanna than in Z. marina due to shorter distances and greater cross-sections of the aerenchyma. The major exchange of O2 across roots of L. dortmanna can be accounted for by small intra-plant resistances to diffusion, larger root than leaf surfaces, and greater radial diffusive resistance of leaves than roots. In contrast, the major O2 exchange across leaves than roots of Z. marina can be accounted for by the opposite anatomical-morphological features. The larger aerenchymal volume and the smaller metabolic rates of L. dortmanna compared to Z. marina imply that turnover of O2 is slower in the aerenchyma of L. dortmanna and O2 fluctuations are more dampened following changes in irradiance. Also, O2 accumulated in the aerenchyma can theoretically support dark respiration for a few hours in L. dortmanna but for only a few minutes in Z. marina. CONCLUSIONS: The build-up of O2 in the pore-water of L. dortmanna sediments during the day as a result of high release of photosynthetic O2 from roots and low O2 consumption of sediments means that sediment, aerenchyma and water are important O2 sources for respiration during the following night, while Z. marina relies on the water column as the sole source of O2 because its sediments are anoxic. These differences between L. dortmanna and Z. marina appear to represent a general difference between the isoetid species mainly inhabiting sediments of low reducing capacity of oligotrophic lakes and the elodeid freshwater species and marine seagrasses mainly inhabiting sediments of higher reducing capacity in more nutrient-rich habitats.     

Growth,biomass distribution and CO2 exchange of northern hardwood seedlings in high and low light: relationships with successional status and shade tolerance

The physiology, morphology and growth of first-year Betula papyrifera Marsh., Betula alleghaniensis Britton, Ostrya virginiana (Mill.) K. Koch, Acer saccharum Marsh., and Quercus rubra L. seedlings, which differ widely in reported successional affinity and shade tolerance, were compared in a controlled high-resource environment. Relative to late-successional, shade-tolerant Acer and Ostrya species, early-successional, shade-intolerant Betula species had high relative growth rates (RGR) and high rates of photosynthesis, nitrogen uptake and respiration when grown in high light. Fire-adapted Quercus rubra had intermediate photosynthetic rates, but had the lowest RGR and leaf area ratio and the highest root weight ratio of any species. Interspecific variation in RGR in high light was positively correlated with allocation to leaves and rates of photosynthesis and respiration, and negatively related to seed mass and leaf mass per unit area. Despite higher respiration rates, early-successional Betula papyrifera lost a lower percentage of daily photosynthetic CO₂ gain to respiration than other species in high light. A subset comprised of the three Betulaceae family members was also grown in low light. As in high light, low-light grown Betula species had higher growth rates than tolerant Ostrya virainiana. The rapid growth habit of sarly-successional species in low light was associated with a higher proportion of biomass distributed to leaves, lower leaf mass per unit area, a lower proportion of biomass in roots, and a greater height per unit stem mass. Variation in these traits is discussed in terms of reported species ecologies in a resource availability context.     

Comparative life history and physiology of two understory Neotropical herbs

Summary Demography and physiology of two broad-leaved understory tropical herbs (Marantaceae) were studied in gaps and shaded understory in large-scale irrigated and control treatments during the dry season at Barro Colorado Island (BCI), Panama. Because photosynthetic acclimation potential may not predict light environments where tropical species are found, we studied a suite of physiological features to determine if they uniquely reflect the distribution of each species. Calathea inocephala and Pleiostachya pruinosa grow and reproduce in gaps, persist in shade, and have equivalent rates of leaf production. Calathea leaves survived 2 to 3 times as long as leaves of Pleiostachya and plants of Pleiostachya were 6 to 8 times more likely to die as plants of Calathea during 3.5 years of study. Pleiostachya had lowest survival in shade and when not irrigated during the dry season, while Calathea survived well in both habitats and both treatments. Pleiostachya had higher photosynthetic capacity and stomatal conductance than Calathea and acclimated to gaps by producing leaves with higher photosynthetic capacity. Calathea had lower mesophyll CO₂ concentrations than Pleiostachya. Both species had similar dark respiration rates and light compensation points, and water-use and nitrogen-use efficiencies were inversely related between species. Species showed no differences in leaf osmotic potentials at full turgor. Calathea roots were deeper and had tuberous swellings.Leaf-level assimilation and potential water loss are consistent with where these species are found, but photosynthetic acclimation to high light does not reflect both species' abilities to grow and reproduce in gaps. Pleiostachya's gap-dependent, rapid growth and reproduction require high rates of carbon gain in short-lived leaves, which can amortize their cost quickly. High rates of water loss are associated with reduced longevity during drought. Calathea's roots may confer greater capacitance, while its leaves are durable, long-lived and have lower water loss, permitting persistence long after gap closure.     

Local weak light induces the improvement of photosynthesis in adjacent illuminated leaves in maize seedlings

To copy with highly heterogeneous light environment, plants can regulate photosynthesis locally and systemically, thus, maximizing the photosynthesis of individual plants. Therefore, we speculated that local weak light may induce the improvement of photosynthesis in adjacent illuminated leaves in plants. In order to test this hypothesis, maize seedlings were partially shaded, and gas exchange, chlorophyll a fluorescence and biochemical analysis were carefully assessed. It was shown that local shading exacerbated the declines in the photosynthetic rates, chlorophyll contents, electron transport and carbon assimilation‐related enzyme activities in shaded leaves as plants growth progressed. While, the decreases of these parameters in adjacent illuminated leaves of shaded plants were considerably alleviated compared to the corresponding leaves of control plants. Obviously, the photosynthesis in adjacent illuminated leaves in shaded plants was improved by local shading, and the improvement in adjacent lower leaves was larger than that in adjacent upper ones. As growth progressed, local shading induced higher abscisic acid contents in shaded leaves, but it alleviated the increase in the abscisic acid contents in adjacent leaves in shaded plants. Moreover, the difference in sugar content between shaded leaves and adjacent illuminated ones was gradually increased. Consequently, local weak light suppressed the photosynthesis in shaded leaves, while it markedly improved the photosynthesis of adjacent illuminated ones. Sugar gradient between shaded leaves and adjacent illuminated ones might play a key role in photosynthetic regulation of adjacent illuminated leaves.     

Response of photosynthesis and respiration of resurrection plants to desiccation and rehydration

Using non-invasive techniques (CO₂ gas exchange, light scattering, light absorption, chlorophyll fluorescence, chlorophyll luminescence), we have analysed the response of respiration and photosynthesis to dehydration and rehydration of leaves of the resurrection plants Craterostigma plantagineum Hochst., Ramonda mykoni Reichb. and Ceterach officinarum Lam. et DC. and of the drought-sensitive mesophyte spinach (Spinacia oleracea L.). The following observations were made: (i) The rate of water loss during wilting of detached leaves of drought-tolerant resurrection plants was similar to that for leaves of the sensitive mesophyte, spinach. Leaves of Mediterranean xerophytes lost water much more slowly. (ii) Below a residual water content of about 20%, leaves of spinach did not recover turgor on rewatering, whereas leaves of the resurrection plants did. (iii) Respiration was less sensitive to the loss of water during wilting in the resurrection plants than in spinach. (iv) The sensitivity of photosynthesis to dehydration was similar in spinach and the resurrection plants. Up to a water loss of 50% from the leaves, photosynthesis was limited by stomatal closure, not by inhibition of reactions of the photosynthetic apparatus. Photosynthesis was inhibited and stomates reopened when loss of water became excessive. (v) After the leaves had lost 80% of their water or more, the light-dependent reactions of photosynthetic membranes were further inhibited by rewatering in spinach; they recovered in the resurrection plants. (vi) In desiccated leaves of the resurrection plants, slow rehydration reactivated mitochondrial gas exchange faster than photosynthetic membrane reactions. Photosynthetic carbon assimilation recovered only slowly.     

High thermal acclimation potential of both photosynthesis and respiration in two lowland Plantago species in contrast to an alpine congeneric

Thermal acclimation of photosynthesis and respiration can enable plants to maintain near constant rates of net CO₂ exchange, despite experiencing sustained changes in daily average temperature. In this study, we investigated whether the degree of acclimation of photosynthesis and respiration of mature leaves differs among three congeneric Plantago species from contrasting habitats [two fast‐growing lowland species (Plantago major and P. lanceolata), and one slow‐growing alpine species (P. euryphylla)]. In addition to investigating some mechanisms underpinning variability in photosynthetic acclimation, we also determined whether leaf respiration in the light acclimates to the same extent as leaf respiration in darkness, and whether acclimation reestablishes the balance between leaf respiration and photosynthesis. Three growth temperatures were provided: constant 13, 20, or 27°C. Measurements were made at five temperatures (6–34°C). Little acclimation of photosynthesis and leaf respiration to growth temperature was exhibited by P. euryphylla. Moreover, leaf masses per area (LMA) were similar in 13°C‐grown and 20°C‐grown plants of the alpine species. In contrast, growth at 13°C increased LMA in the two lowland species; this was associated with increased photosynthetic capacity and rates of leaf respiration (both in darkness and in the light). Alleviation of triose phosphate limitation and increased capacity of electron transport capacity relative to carboxylation were also observed. Such changes demonstrate that the lowland species cold‐acclimated. Light reduced the short‐term temperature dependence (i.e. Q₁₀) of leaf respiration in all three species, irrespective of growth temperature. Collectively, our results highlight the tight coupling that exists between thermal acclimation of photosynthetic and leaf respiratory metabolism (both in darkness and in the light) in Plantago. If widespread among contrasting species, such coupling may enable modellers to assume levels of acclimation in one parameter (e.g. leaf respiration) where details are only known for the other (e.g. photosynthesis).     

A hemiparasite in the forest understorey: photosynthetic performance and carbon balance of Melampyrum pratense

• Melampyrum pratense is an annual root‐hemiparasitic plant growing mostly in forest understorey, an environment with unstable light conditions. While photosynthetic responses of autotrophic plants to variable light conditions are in general well understood, light responses of root hemiparasites have not been investigated.
• We carried out gas exchange measurements (light response and photosynthetic induction curves) to assess the photosynthetic performance of M. pratense in spring and summer. These data and recorded light dynamics data were subsequently used to model carbon balance of the hemiparasite throughout the entire growth season.
• Summer leaves had significantly lower rates of saturated photosynthesis and dark respiration than spring leaves, a pattern expected to reflect the difference between sun‐ and shade‐adapted leaves. However, even the summer leaves of the hemiparasite exhibited a higher rate of light‐saturated photosynthesis than reported in non‐parasitic understorey herbs. This is likely related to its annual life history, rare among other understorey herbs. The carbon balance model considering photosynthetic induction still indicated insufficient autotrophic carbon gain for seed production in the summer months due to limited light availability and substantial carbon loss through dark respiration.
• The results point to potentially high importance of heterotrophic carbon acquisition in M. pratense, which could be of at least comparable importance as in other mixotrophic plants growing in forests – mistletoes and partial mycoheterotrophs. It is remarkable that despite apparent evolutionary pressure towards improved carbon acquisition from the host, M. pratense retains efficient photosynthesis and high transpiration rate, the ecophysiological traits typical of related root hemiparasites in the Orobanchaceae.

     

The photosynthesis of ryegrass leaves grown in a simulated sward

Plants were taken from simulated swards of perennial ryegrass (Lolium perenne) grown in a controlled environment and the rates of photosynthesis of the youngest fully expanded leaves, and the second and third youngest leaves on the same tillers were measured. The youngest leaves had the highest rates and the third the lowest, with the second leaves intermediate. The rate of photosynthesis in bright light of successive youngest expanded leaves decreased as the swards increased in leaf area, but did not when plants were grown so that the main stem was not shaded. When plants were grown at different densities and the photosynthetic rates of leaves of a particular ontogenetic rank were measured, it was found that leaves on plants from higher densities had lower rates of photosynthesis. Also leaves on plants grown in bright light had higher photosynthetic rates than those on plants grown in dim light. It is concluded that the decline in the photosynthetic capacity of successive leaves in a rapidly growing simulated sward is due to the intense shading to which they are subjected during their expansion.     

Carbohydrate storage and use in an alpine population of the perennial herb, Oxytropis sericea

I tested hypotheses for ecological roles of storage carbohydrates in perennating organs (roots and branches) of alpine Oxytropis sericea, a leguminous herb. In naturally growing plants, total nonstructural carbohydrates achieved their maximal concentration in the fall, declined during winter, and reached minimal levels immediately after growth initiation in the spring. Experimental manipulation of carbon sink-source relations through shading of leaves of reproductive plants revealed that the normally unused portion of these carbohydrates is largely available for withdrawal. In another experiment, plants subjected to carbohydrate depletion through shading suffered decreased leaf growth after winter dormancy and had a lower probability of flowering and decreased inflorescence biomass. The dependence of reproductive growth on stored carbohydrates, however, was limited to its initial stages, because accumulation of storage carbohydrates occurred simultaneously with inflorescence expansion, flowering, and fruiting. Moreover, the whole-plant photosynthetic rate, estimated from gas exchange measurements also peaked at the time of inflorescence growth. To address whether stored reserves allow compensatory regrowth following defoliation, plants were subjected to experimental removal of leaves and inflorescences. Defoliated O. sericea partly regrew the lost leaves but withdrawal of stored carbohydrates was limited. Similarly, in a second defoliation experiment where infructescences were left intact, the plants used little stored carbohydrate and only partly compensated for fruit growth. However, carbohydrate accumulation was negatively affected by defoliation. While the ecological importance of stored nonstructural carbohydrates cannot be attributed to any function in isolation, winter respiration, leaf regrowth after winter, and early reproductive growth in O. sericea all depend to a significant extent on stored reserves. Maintaining a large storage pool may protect these functions in years when carbon status is less favorable than during this study. Received: 13 May 1998 / Accepted: 24 November 1998     

Photosynthesis and dark respiration of leaves of terrestrial carnivorous plants

Using CO₂ gasometry, net photosynthetic (P _N) and dark respiration rates (R _D) were measured in leaves or traps of 12 terrestrial carnivorous plant species usually grown in the shade. Generally, mean maximum P _N (60 nmol CO₂ g⁻¹(DM) s⁻¹ or 2.7 μmol m⁻² s⁻¹) was low in comparison with that of vascular non-carnivorous plants but was slightly higher than that reported elsewhere for carnivorous plants. After light saturation, the facultatively heliophytic plants behaved as shade-adapted plants. Mean R _D in leaves and traps of all species reached about 50% of maximum P _N and represents the high photosynthetic (metabolic) cost of carnivory.     

Temperature and light: The determining factors in maximum depth distribution of aquatic macrophytes in Ontario,Canada

In stratified lakes with high light penetration, the maximum depth at which macrophytes occur is frequently limited by temperature. At this depth a variety of species may be found. On the other hand, when the clarity of water limits the light penetration and the temperature at depth is sufficient for good plant growth, the plants occurring at greatest depth are ones that do not require photosynthetic oxygen for root growth. Such plants include the Charales, Isoetes, Utricularia and Ceratophyllum.