Differences in the Interacting Effects of Light and Temperature on Growth of Four Species in the Vegetative Phase

A comparative study, employing the concepts of growth analysis,has been made of the varying responses in the early vegetativephase of Gossypium hirsutum, Helianthus annuus, Phaseolus vulgaris,and Zea mays to combinations of light intensity (1.08, 2.16,3.24, 4.32, and 5.4 x 10⁴ lx—photoperiod 14 h) and constantdiurnal air temperatures (10, 15, 20, 25, 30, and 35 °C).Depending on the combination of treatments, the temperatureof the internal tissues departed from air temperature by 6.9to 1.4 °C: so only the internal temperatures are cited here. For each species there are complex interactions between theeffects of light and temperature on the net assimilation rate,the leaf-area ratio, and the relative growth-rates of plantweight and leaf area. The magnitude of the changes induced bythe two factors vary both with the growth component and thespecies. The temperature responses are maximal up to 20–5°C while at the highest temperatures they may be negative.The temperature coefficients for leaf-area ratio are consistentlyless than those of the other three components: here betweenspecies the coefficients over 10–20 °C vary by a factorof 9.6, 5.4, and 5.1 for the rates of gain in plant weight andleaf area and the net assimilation rate, while the orderingwithin each growth component is species dependent. Under conditions of optimal temperature the relative growth-rateand net assimilation rate progressively increase, accordingto the species, up to either 4.32 or 5.4x 10⁴ lx. The leaf-arearatio is always largest at the lowest intensity. The level oflight at which the rate of gain in leaf area reaches a maximumranges from 2.16x 10⁴ lx for Phaseolus to between 4.32 and 5.40x10⁴ lx for Gossypium. The highest relative growth-rate and net assimilation rate ofHelianthus exceed those of Zea substantially. Indeed the maximalassimilation rate for Helianthus of 2.10 g dm^–2 week^–1is the highest ever recorded under field or controlled conditions.Possible reasons for this reversal of the photosynthetic potentialsof the two species observed by previous workers are discussed.     

The Effect of Temperature on Vegetative Growth in Climatic Races of Dactylis glomerata in Controlled Environments

The growth patterns in two natural populations of Dactylis glomeratafrom contrasting climatic regions, Norway and Portugal, werestudied at four constant temperatures (5, 10, 20, and 30°C) in a 16-h photoperiod. Marked changes in relative growth-rateat different temperatures were positively correlated with changesin both net assimilation rate and leaf-area ratio, whereas differencesbetween the populations in the relative growth-rate were theresult of differences in net assimilation rate, and were negativelycorrelated with differences in leaf-area ratio. The changesin leaf-area ratio at different temperatures were correlatedwith changes in leaf morphology and distribution of assimilateswithin the plant. The possible adaptive advantage of these vegetativegrowth patterns is discussed in relation to the survival ofthe plants in the original environments.     

An Analysis of Plant Growth and its Control in Arctic Environments

The relative growth-rate of plants grown on a vermiculite culturemedium in an arctic climate during the growing season was abouta quarter of that of comparable plants on the same medium ina temperate climate. In both climates the relative growth-ratewas lower on natural soils than on vermiculite. Net assimilationrates and, to a lesser extent, leaf-area ratios were depressedby arctic climates and soils. Net assimilation rates of seven species in various habitatsin two arctic regions were about 0.1–0.3g dm^–2wk^–1.Previous suggestions that net assimilation rates in arctic regionsequal or exceed those in temperate regions are attributed tomisinterpretation of data or to inadequate methods. There is evidence that the depression of net assimilation ratesin arctic regions is due to the low temperatures, which, especiallywhen associated with soil nitrogen deficiency, reduce the rateat which assimilates are used in respiration and new growth;this causes sugars to accumulate to levels at which they depressassimilation.     

Effect of Temperature on Net Assimilation Rate

Net assimilation rates and other growth attributes were comparedfor rape, sunflower, and maize plants growing widely spacedat temperatures of 10°, 16°, 22°, 28°, and 34°C, in light of 3, 000 f.c. intensity. The optimum temperature for net assimilation rate lay between20° and 30° C, and was lowest for rape and highest formaize. The temperature coefficient of the net assimilation ratewas lower than that of the relative growth-rate, especiallyin rape and sunflower, corresponding to an increase in leaf-arearatio with in temperature. This arose to an increase in leaf-arearatio with rise in temperature. This mcrease arose through changeinleafarea/leaf weight; temperature had little effect on leafweight/plant weight. In moderate to warm conditions the net assimilation rate variedlittle with temperature: by only± 10 per cent between12° and 30° C for rape, and 23° and 36° C formaize. This agrees with observations in natural climates whichsuggest that temperature is generally less important than lightin controlling net assimilation rates, except in cool climates.In natural climates, as in these controlled climates, relativegrowth-rate is more temperature-dependent.     

Further Effects of Light Intensity, Carbon Dioxide Concentration, and Day Temperature on the Growth of Chrysanthemum morifolium cv. Bright Golden Anne in Controlled Environments

In earlier work the effects of light intensity over the range31 to 250 J cm^–2 day^–1 and carbon dioxide concentrationfrom 325 to 900 ppm with 8-h days at 18.3 °C and 16-h nightsat 15.6 °C were described. The present paper is concernedwith three further experiments with light levels up to 375 Jcm^–2 day^–1 (which corresponds to the daily totalin a glasshouse in southern England in early May or August andthe intensity is approximately that of mid-winter sunshine),carbon dioxide concentration up to 1500 ppm, and day temperaturesof 18.3 to 29.4 °C. Final plant weight was increased by light over the range 125–375J cm^–2 day^–1 and by carbon dioxide over the range325–900 ppm, with positive interaction between them; thisinteraction was increased by raising the temperature to 23.9°C and somewhat more at 29.4 °C day temperature. Leaf-arearatio and specific leaf area were reduced by increasing eitherlight or carbon dioxide but there was little effect of temperature.Leaf-weight ratios were uniform within experiments but therewere small consistent differences between one experiment andthe other two which also affected leaf-area ratios. Mean unit leaf rate was scarcely affected by day temperatureover the range investigated. There were the usual increasesdue to increased light and carbon dioxide concentration anda consistent difference in absolute value between one experimentand the other two. These differences in mean unit leaf rateare illustrated in detail in the ontogenetic trend of unit leafrate and plant size. Lower unit leaf rates were to a considerableextent compensated for by increased leaf-area ratios in theusual way. Despite the substantial differences in day temperature the specificwater contents (g water g dry weight^–1) differed little,showing in the majority of cases higher values in the highertemperature for otherwise similar treatment combinations. Flower development was somewhat delayed at 23.9 °C day temperature,and substantially so at 29.4 °C. Lateral branch length wasincreased at 23.9 °C and excessively so at 29.4 °C.This reveals quite clearly that a temperature optimum for vegetativegrowth may not be the optimum for flowering performance norproduce a desirable plant shape. Despite the marked effects of temperature on rate of flowerdevelopment, the relationship between flower development andthe ratio of flower to total weight was the same for all treatmentcombinations in all three experiments and coincident with thatreported earlier. Gasometric determinations indicated that respiratory loss bythe whole plant was a smaller proportion of net photosyntheticgain at a temperature of 29.4 °C than at 18.3 °C andwas likewise a smaller proportion at 1500 ppm carbon dioxidethan at 325 ppm. If photorespiration of leaves is assumed tobe as great as their dark respiration, the respiratory lossesare in the range of 31–50 per cent of the gross gain.Greater rates of photorespiration would increase the proportionaterespiratory loss.     

Growth Analysis of Sweet Pepper (Capsicum annuum L.): 2. Interacting Effects of Irradiance, Temperature and Plant Age in Controlled Conditions

A growth analysis was carried out with sweet pepper plants grownin a phytotron. Irradiance conditions were: 0.84 or 3.25 MJm^–2 in 8 h, 1.67 MJ m^–2 in 16 h and 2.51 MJ m^–2in 24 h. Temperatures applied were 25 or 21 °C during thephotoperiod in combination with 25, 21 and 17 or 21, 17 and13 °C respectively during the nyctoperiod. Highest values for leaf area and total dry weight were foundwhen applying 1.67 MJ m^–2 in 16 h, followed by 3.25 MJm^–2 in 8 h, irrespective of the temperature regime. Continuousirradiance ultimately resulted in leaf drop. A reduction inthe day temperature decreased leaf area and total dry weight.At a day temperature of 25 °C the dry weight increased withdecreasing night temperature when applying 3.25 MJ m^–2in 8 h. At a day temperature of 21 °C leaf area and dryweight were reduced when 17 or 13 °C were applied duringa 16 h nyctoperiod. Values for relative growth rate, net assimilation rate, leafarea ratio and leaf weight ratio strongly decreased with advancingplant age. The effects of irradiance treatment on RGR and NARwere analogous to those on total dry weight while the reversepattern was observed for the LAR. A decrease in day temperaturedecreased the RGR. The effects of night temperature exhibitedstrong interactions with day temperature and photoperiod. Theinfluence of temperature on RGR was largely mediated throughchanges in the LAR. The latter parameter was highly correlatedwith the specific leaf weight. Capsicum annuum L., sweet pepper, growth analysis, irradiance, temperature, plant age     

Physiological and Ecological Studies in the Analysis of Plant Environment: XII. The Role of the Light Factor in Limiting Growth

Previous investigations in southern England on twenty-two herbaceousspecies have demonstrated that for widely spaced plants thediurnal solar radiation limits the net assimilation rate ofall species and restricts the relative growth rate of many.In examining how far these limitations apply to other environmentsit is now shown that in the subtropics and tropics the levelsof net assimilation rate and relative growth rate can greatlyexceed those so far recorded for cool temperate regions, andthese differences are attributed to the higher insolation andtemperatures. From a variety of evidence it is concluded that as the distancebetween plants is reduced 8O the net assimilation rate is progressivelydiminished even in regions of high insolation through the enhancedmutual shading. In consequence levels of light which may besupra-optimal for relatively isolated individuals may yet limitthe dry-matter production of a dense population. There is anoptimal ratio of leaf area to ground surface (leaf-area index)for the maximal exploitation of the incoming radiation in carbonfixation by the population and this optimum will vary with thespecies and the light intensity. Where other environmental factorsare favourable, light may limit dry-matter production everywhere. On an annual basis dry-matter production will be dependent ontwo components—the length of the ‘growing season’and the period over which the leaf-area index remains optimal.In the tropics the highest annual rate of production so farrecorded is 7⁸ tonnes/hect. produced by Saccharum officinarumandin north-east Europe 23.5 tonnes by Fagus sylvatica. Over shortperiods the rate of dry-matter production can attain 3⁸g./m.²/dayand the utilization of solar energy can be as high as 4.2 percent., or 9.5 per cent, for the range 4, 000–7, 000 A. Although information on the productivity of natural communitiesis still ex-ceedingly scanty, an attempt has been made to interpretthe general pattern in terms of the length of the growing season,the level of solar radiation, the magni-tude of the leaf-areaindex of the whole community, and the period over which theleaf canopy remains green. It is postulated that in any regionthe vegetation reaches a dynamic equilibrium when there is themaximum exploitation of the incoming radiation to produce thegreatest production of dry matter.     

Effect of Photoperiod on Growth of Sugar Beet

Sugar beet grown in controlled environments were given similardaily amounts of visible radiation during three different photoperiodtreatments. Plants were given (a) 115 W m^–2 visible irradiancefrom fluorescent and tungsten lamps for 12 h; (b) 88 W m^–2of the same light for 16 h or (c) 115 W m^–2 from fluorescentand tungsten lamps for 12 h extended to 16 h with low intensity(3 W m^–2) incandescent light from the tungsten lamps only.Plant growth was increased similarly in both long day treatments[(b) and (c)] and dry weights were 25 per cent greater thanin the 12 h photoperiod (a) after 6 weeks. Leaf area was increasedby 18 per cent and net assimilation rate by 10 per cent in the16 h photoperiod at 88 W ^m–2 (b). By contrast, extendingthe photoperiod with 4 h of incandescent light (c) triggereda photomorphogenic increase in leaf expansion which increasedleaf area per plant by 47 per cent and leaf-area ratio by 12per cent.     

Effect of Light Intensity, Carbon Dioxide Concentration, and Leaf Temperature on Gas Exchange of Spray Carnation Plants

The rates of CO₂ assimilation by potted spray carnation plants(cv. Cerise Royalette) were determined over a wide range oflight intensities (45–450 W m^–2 PAR), CO₂ concentrations(200–3100 vpm), and leaf temperatures (5–35 °C).Assimilation rates varied with these factors in a way similarto the response of single leaves of other temperate crops, althoughthe absolute values were lower. The optimal temperature forCO₂ assimilation was between 5 and 10 °C at 45 W m^–2PAR but it increased progressively with increasing light intensityand CO₂ concentration up to 27 °C at 450 W m^–2 PARand 3100 vpm CO₂ as expressed by the equation TOpt = –6.47-h 2.336 In G + 0.031951 where C is CO₂ concentration in vpmand I is photo-synthetically active radiation in W m^–2.CO₂ enrichment also increased stomatal resistance, especiallyat high light intensities. The influence of these results on optimalization of temperaturesand CO₂ concentrations for carnation crops subjected to dailylight variation, and the discrepancy between optimal temperaturesfor growth and net photosynthesis, are discussed briefly     

Physiological and Ecological Studies in the Analysis of Plant Environment: XIII. A Comparison of the Effects of Seasonal Variations in Light Energy and Temperature on the Growth of Helianthus annuus and Vicia faba in the Vegetative Phase

The influences of seasonal changes in light radiation and temperatureon the vegetative growth of Helianthus annuus and Vicia fabahave been investigated in the east of Scotland by pot experiments,carried out in the open at weekly intervals between June andSeptember in 1956 and May and October in 1957. To minimize theeffects of ontogenetic drift pots containing plants of a similarmorphological status were selected from batches sown every fewdays. At the beginning and end of each experiment replicatedand paired pots were harvested and the dry weights of the leaves,stems, and roots together with the leaf areas determined. Fromthese data weekly values for net assimilation rate, leaf-arearatio (ratio of leaf area to plant weight), and relative growthrate were calculated. Simultaneously, records were kept of the diurnal changes inair temperature and of light energy by means of an integratingphotometer. Multiple regressions linking light and temperature with netassimilation rate, leaf-area ratio, and relative growth ratewere calculated separately for each year. A significant ‘time-of-season’trend was largely eliminated by including an additional variable,the initial leaf-area ratio. In the individual regressions thevariance accounted for was very high, ranging from 75 to 97per cent. The results demonstrated that for both species the net assimilationrate and relative growth rate were positively dependent on lightand temperature. The leaf-area ratio of both species was negativelyaffected by light, but only for V. faba was there a positiverelationship between the leaf-area ratio and temperature. H.annuus grew faster than V. faba during the major part of theseason, largely because of its higher leaf-area ratio. The results are compared with prior investigations in Englandand elsewhere.     

Developmental Physiology of Sugar Beet: I. THE INFLUENCE OF LIGHT AND TEMPERATURE ON GROWTH

Sugar beet plants were grown for 12 weeks from emergence ingrowth rooms at temperatures of 10, 17, 24 and 31 °C and20, 50, 80, and 110 cal visible radiation cm^-2d^-1, and the changeswith time in their dry weight, leaf area, leaf numbers, andstorage root sugar determined. The first stage of growth wasdominated by the development of the shoot, but the storage rootgradually assumed increasing importance and eventually grewat a faster rate and to a greater weight than the shoot. Therelative growth rate and final yield of dry matter of the shootwere greatest at 24 °C and of the root between 17 and 24°C. The relative rate of expansion and the final area ofthe leaf surface were also greatest at 24 °C, whilst therates of production and of unfolding of leaves were greatestat about 17 °C. All these attributes were increased withincreased radiation. Net assimilation rate increased almostproportionately with radiation and was not significantly affectedby temperature.The relationships of total leaf area with plantdry weight, root dry weight with shoot dry weight, and totalleaf number with plant dry weight were scarcely affected bychanges in radiation, but were much influenced by temperature.Plants of the same dry weight generally had bigger roots andsmaller areas of leaf surface as temperatures departed from24 °C and had most leaves at 17 °C. Sugar concentrationsin the storage root were greatest at 17 °C, but the totalamount of sugar was about the same at 17 and 24 °C. Theconcentration of sugar in the storage root depended on rootsize.Thus, temperature affected both the rate and pattern ofdevelopment, and radiation affected the rate but not the patternof development.     

Growth Responses of Two Solanum Species to Contrasting Temperatures and Irradiance Levels: Relations to Photosynthesis, Dark Respiration and Chlorophyll Fluorescence

Potato production in the tropical lowlands during the rainyseason is constrained by high temperature and low irradiance.This study examined the effect of these two variables on drymatter production and allocation, using plant growth, leaf anatomy,gas exchange and chlorophyll fluorescence measurements. Plantsof two clones, Solanum goniocalyx cv. Garhuash Huayro (GH) andDTO-33, a heat tolerant clone of S. tuberosum x S. phureja,were grown in growth chambers at 33/25 °C or 20/10 °Cday/night temperature. At each temperature, plants were grownin either 12 h high irradiance (430–450 µmol m^–2s^–1 PAR) or 12 h low irradiance (250–280 µmolm^–2 s^–1) both with a 6–h photoperiod extensionof 6 µmol m^–2 s^–1. Plants were harvested after10 d (initial harvest) and after 20 d (final harvest). By theend of the study DTO-33 had produced more dry matter and hadtuberized, whereas GH had a greater leaf area ratio (LAR) andspecific leaf area (SLA). The highest relative growth rate (RGR)was at low temperature and low irradiance, possibly due to acombination of thin leaves with a large surface area. At thehigh temperature, low irradiance had the opposite effect, producingthe lowest net assimilation rate (NAR) and lowest RGR. Bothtuber number and weight were markedly reduced by high temperature.Low irradiance, in combination with high temperature, producedvirtually no tubers. Stomatal density, which was greater onGH than in DTO-33, was increased at high temperature. When measuredat 30 °C both clones, especially DTO-33, showed heat-adaptationin terms of ability to maintain a high rate of net photosynthesisat 30 °C. Plants grown at high irr-adiance and low temperaturehad the lowest net photosynthetic rate at 30 °C. Concurrentmeasurements of chlorophyll fluorescence indicated that onlythe initial (O) fluorescence parameter was affected. The dataconfirm the field observation that reduction in potato growthat high temperature can be aggravated by lower irradiance. Thisreduction is associated with a reduced leaf area and NAR. Growth analysis, heat adaptation, light     

Changes in the Growth of Salvinia natans Induced by Cycles of Light and Darkness of widely Different Duration

The growth of Salvinia natans has been examined when clonalmaterial, maintained at a constant temperature (30 ^°C) receivesthe same amount of light energy per day but where the light-darkcycle of equal intervals varies in eight steps from 1 min to12 h. The area per leaf, the rate of leaf production, the netassimilation rate, and the relative growth-rate increase withthe lengthening of the cycle, but the leaf-area ratio is reduced.The magnitude of the changes differs between the criteria whilethe order of the response may be disparate between consecutiveintervals. In supporting experiments the same measurements weremade on plants subjected to a wide range of light intensitieswith a common photoperiod of 12 h. Here decreasing light intensityproduces similar trends to those recorded for increasing thelength of the cycle but the patterns of response may diverge.It was also established that the size of the stomatal pore isthe same in the light and in the dark. It is postulated thatvanations in the light-dark cycle may influence both the levelof photosynthetic activity and the pathways.     

Effect of Photoperiod on Vegetative Growth in Two Natural Populations of Dactylis glomerata L.

The growth of two natural populations of cocksfoot from contrastingclimatic regions (Norway and Portugal) was studied at four temperaturesand two photoperiods. Serial harvests were taken and quadraticcurves were fitted to log dry weight and leaf area for eachreplicate in order to calculate growth attributes at a constantplant weight for all treatments. Interactions of population,temperature, and photoperiod on relative growth-rate (RGR) werefound, with the greatest population differences at 5 and 30°C in an 8-h photoperiod. Leaf-area ratio (LAR) played alarger part than net assimilation rate (NAR) in determiningthe differential population responses in RGR to daylength, andthese differences in LAR were primarily the result of differentpatterns of dry-matter distribution within the plant.     

Effect of Light Intensity on Growth of Natural Populations of Dactylis glomerata L.

The growth of two natural populations of cocksfoot from contrastingclimatic regions, Norway and Portugal, was studied in two photoperiodsat three temperatures with three levels of light energy (48,144, and 240 W m^–2 in the wavelength interval 400–700nm). There was a consistent increase in relative growth-rate(RGR) in response to increased light energy up to 144 W m^–2,but above this energy level there was either no change, or,in some treatments, a decline. Net assimilation rate (NAR) increased,whilst leaf area ratio decreased from the lowest to the highestenergy level in most treatments. The decrease of LAR with increasedlight energy could be attributed to a decrease of both leafweight ratio (LWR) and specific leaf area (SLA), a greater proportionof dry matter being distributed to plant parts other than leaf.This effect occurred although there was a positive relationshipbetween light energy and relative leaf growth-rate (RLGR). Populationdifferences in these growth attributes were most marked in thetreatments with low-temperature and short-day conditions. Theefficiency of energy conversion of visible radiation declinedfrom 3–4 per cent at the lowest energy level to 1–2per cent at the highest energy level.     

Effects of CO2-Enrichment on the Growth of Young Tomato Plants in Low Light

Carbon dioxide-enrichment of young tomato plants grown in controlled-environmentcabinets at low light intensity (14 cal cm^–2 day^–1,visible radiation) increased their net assimilation rates and,initially, relative growth-rates. Subsequently, the relativegrowth-rate fell to near the rate of non-enriched plants, owingto a fall in leaf-area ratio associated with an increase inleaf dry weight/area. Sowing non-enriched plants a few daysearlier to reach the same total dry weight would not have producedidentical plants. The effects of CO₂-enrichment to 1000 vpm could be simulatedby increasing light intensity by approximately one third exceptthat the plants had shorter internodes than those in extra CO₂.This was a morphogenetic effect of light since CO₂-enrichmentitself produced slightly shorter plants than controls for anequivalent total dry weight. CO₂-enrichment did not change the dry-weight distribution inthe plants and had little effect on rate of leaf produoctionor the number of flower primordia. There were no indicationsthat beneficial effects of CO₂-enrichment operated other thanthrough increased photosynthesis.     

The Potential for Photoinhibition of Pinus sylvestris L. Seedlings Exposed to High Light and Low Soil Temperature

The effect of high light and root chilling on gas exchange,chlorophyll fluorescence, and bulk shoot water potential (_shoot)was examined for Pinus sylvestris seedlings. Transferring plantsfrom low light (200 µmol m^–2s^–1, PAR) anda soil temperature of 15 °C to high light (850 µmolm^–2 s^–1) and 1 °C caused >90% decrease innet photosynthesis and leaf conductance measured at 350 mm³dm^-3 CO₂, and a decrease in the ratio of variable to maximumfluorescence (F_v/F_m) from 0.83 to 0.63. The decrease in Fv/Fmwas, however, only marginally greater than when seedlings weretransferred from low to high light but kept at a soil temperatureof 15 °C. Thus, photoinhibition was a minor component ofthe substantial decrease observed for net photosynthesis at1 °C soil temperature. The decrease in net photosynthesisand _shoot at 1 °C was associated with an increase in calculatedintracellular CO₂ concentration, suggesting that non-stomatalfactors related to water stress were involved in inhibitingcarbon assimilation. Measurements at saturating external CO₂concentration, however, indicate that stomatal closure was thedominant factor limiting net photosynthesis at low soil temperature.This interpretation was confirmed with additional experimentsusing Pinus taeda and Picea engelmannii seedlings. Decreasesin gas-exchange variables at 5 °C soil temperature werenot associated with changes in _shoot Thus, hormonal factors,localized decreases in _needles or changes in xylem flux maymediate the response to moderate root chilling.     

An Analysis of Growth of Oil Palms under Nursery Conditions: I. Establishment and Growth in the Wet Season

Growth of oil palm seedlings over the period 2–31 weeksafter planting in the nursery was studied using growth-analysistechniques. Curves of the Gompertz type were fitted to the basicdata of plant dry weight and leaf area, and from the equationsof the fitted curves, net assimilation rate (E_A), relative growth-rate(Rw), and relative leaf growth-rate (R_A) were calculated. The low values of E_A (0.16-0–31 g/dm²/week) and Rw (1.4–2.2per cent./per day) confirm earlier work on oil palm seedlings.The time trend of increasing E_A and R_W over the period studiedis associated with steadily increasing solar radiation overthe second half of the period. Leaf-area ratio is markedly affected by transplanting, and asthis unbalance of leaf area/total dry weight has been shownto be associated with low rates of EA in seedlings, it is suggestedthat the low values of E_A and R_W in the first half of the experimentalperiod are due to the effect of transplanting. These findings are discussed in relation to current nurserypractice.     

Effect of Water Stress on Gas Exchange in Fronds of the Ostrich Fern (Matteuccia struthiopteris (L.) Todaro)

Experiments were conducted in a gas exchange system to examinethe effect of a water stress, induced by –200 kPa polyethyleneglycol (PEG), on carbon dioxide and water vapour flux, fronddiffusive resistance, intercellular carbon dioxide concentration,carbon dioxide residual resistance and frond water potentialin the ostrich fern (Matteuccia struthiopteris (L.) Todaro).Measurements were taken 1 d after the application of PEG. Themeasurements were made on young fronds (8 d old) and maturefronds (20–24 d old) at PPFD's (Photosynthetic PhotonFlux Density) from 0–1400 µmol m^–22 s^–1.Water stress decreased the net photosynthesis rate in maturefronds at PPFD's of 210 µmol m^–2 s^–1 or greaterand increased the net photosynthesis rate below 210 µmolm^–2 s^–1 in young fronds. The increase in net photosynthesisin stressed young fronds was associated with a significant reductionin the dark respiration rate. Water stress and decreasing PPFD'sincreased frond diffusive resistance. Carbon dioxide concentrationin the intercellular spaces decreased with increasing frondage and PPFD's up to 200 µmol m^–2 s^–1. Theresidual resistance to carbon dioxide flux was not significantlyaffected by either frond age or water stress. Frond water potentialwas significantly lower in mature fronds than in young fronds. Key words: Matteuccia struthiopteris, Water relations, Photosynthesis, Dark respiration     

Physiological and Ecological Studies in the Analysis of Plant Environment: VII. An Analysis of the Differential Effects of Light Intensity on the Net Assimilation Rate, Leaf-Area Ratio, and Relative Growth Rate of Different Species

Since relative growth rate is the product of net assimilationrate and leaf-area ratio (leaf area/plant weight), it followsthat if the effects of shading on both net assimilation rateand leaf-area ratio can be expressed mathematically, then therelationship between light intensity and relative growth ratecan be derived from the product of the two mathematical expressions. For all the ten species investigated in field and pot cultureexperiments, it has been found that during the early vegetativephase both the changes in leaf-area ratio and net assimilationrate, over the range of 0·1 to full daylight, are linearlyrelated to the logarithm of the light intensity. In consequence,the relationship between relative growth rate and the logarithmof light intensity—being the product of the two linearregressions—is curvilinear. For species of shady habitats (Geum urbanum, Solamun dulcamara)neither the levels of assimilation rate nor the ‘compensation-point’values are very different from those of the eight species fromopen situations (e.g. Hordeum vulgare, Pisum sativum, Fagopyrumesculentum). Nevertheless the intensity at which growth rateis maximal varies between species: it is 0•5 for G. urbanum,0•7 for H. annuus, full daylight for F. esculentum, whilefor Trifolium subterraneum the calculated value is 1·8daylight. Such specific differences can be largely accountedfor in terms of the differences in leaf-area ratio at the differentlight levels. On the basis of this analysis of the light factor, a ‘shade’plant is best redefined as a species in which a reduction ofthe light intensity causes a rapid rise in the leaf-area ratiofrom an initial low value in full daylight: for a ‘sun’plant the converse definition holds.