共查询到20条相似文献,搜索用时 31 毫秒
1.
Derivation of Pressure-Volume Curves by a Non-Linear Regression Procedure and Determination of Apoplastic Water 总被引:1,自引:0,他引:1
Data from pressure-volume (PV) analysis may be submitted totransformation I [i.e. leaf water potential (1) versus inverserelative water content (1/R)] or to transformation II (i.e.1/1 versus R). This may cause an essential distortion of theerror structure especially in transformation II due to the relativelylarge range which is to be covered by the 1/1 ratio. Similarly,logarithmic transformation of leaf turgor potential (P) whenderiving the sensitivity factor of elasticity (ß)by linear regression from values of In p and 1/R may distortthe error structure. In order to investigate the magnitude ofthe distortion effect on parameters derived from PV analysisby regression a non-linear regression procedure was comparedwith the common linear procedure when calculating p from ßin the turgid region and leaf osmotic potential (P) in boththe turgid and non-turgid region. As test plants we used fieldgrown species of spring barley (Hordeum distichum L., cvs Gunnarand Alis). The results show that transformations and applicationof linear regression procedures distort the error structureof p more than the error structure of ', which was only slightlyaffected. However, we recommend the use of the non-linear procedurein both cases. Furthermore, from PV analysis, obtained by thermocouple hygrometryon living and killed leaf tissue, respectively, we derived themathematical basis for calculating the apoplastic water fraction(Ra). Ra was 0.15 at R= 1 and decreased with dehydration. The equations describing the relation between and R and betweenp and R were extended to take into account the apoplastic waterfraction. Key words: Apoplastic water, distortion errors, non-linear regression, pressure-volume curves 相似文献
2.
The Meaning of Matric Potential 总被引:6,自引:1,他引:5
The commonly used equation, = P - + , which describes thepartitioning of plant water potential, , into components ofhydrostatic pressure, P, osmotic pressure, , and matric potential,, is misleading. The term , which is supposed to show the influenceof a solid phase on , is zero if a consistent definition ofpressure is used in the standard thermodynamic derivation. However,it can be usefully defined by = + D, where D is the osmoticpressure of the equilibrium dialysate of the system. The practicaland theoretical significance of this definition is discussed. 相似文献
3.
An error occurs in the calibration of xylem pressure potential() against leaf-water potential () when the calibration is madeusing plant material in which the water stress has been inducedartificially after excision. The impostion of water stress afterexcision affects the determination more than it affects , consequentlythe relationship between these two indices of water stress isaltered. Care should be exercised to ensure that identical proceduresare adopted during . calibrations and during susbsequent fieldmeasurements of with the pressure-chamber apparatus. 相似文献
4.
In recent years alternative ways have been proposed to transformmeasurements of leaf water potential, , and relative water content,R*, in order to derive values of osmotic pressure at full turgidityin leaves and shoots, o(when 0). Two types of transformationsare usually considered: 1/ versus R* and versus 1/R*, and linearregression is used to fit the data in the region where turgoris thought to be zero. It appears that when o is estimated bylinear extrapolation of 1/Psi; versus R* then apoplastic watermight not influence the accuracy of o but when the versus \/R*transformation is used apoplastic water causes an underestimateof o. We examine the accuracy of the estimate of o obtainedfrom the two transformations when there are random errors in, systematic errors in , and when the osmotic solutions arenon-ideal. The 1/ versus R* transformation generally producesthe best estimate of 0 by linear extrapolation. 相似文献
5.
An equation is derived expressing average turgor pressure ofa leaf (p) as a function of relative water content (RWC). Basedon this derivation, the relationships of the bulk elastic modulus(v) and both RWC and p, are formulated and discussed. The bulkelastic modulus (v) becomes zero for p = 0, that is at the turgorloss point for the leaf. At full water saturation the valueof ev is proportional to the water saturation turgor potentialp(max). The factor relating P and v (structure coefficient ,Burstrom, Uhrstr?m and Olausson, 1970) changes only very littlefor values of p, which are not too close to zero. An exampleis given for the calculation from experimental data of the turgorpressure function, the structure coefficient function, and thev function. Key words: Cell wall, Turgor pressure, Bulk elastic modulus 相似文献
6.
Changes in components of leaf water potential during soil waterdeficits influence many physiological processes. Research resultsfocusing on these changes during desiccation of peanut (Arachishypogeae L.) leaves are apparently not available. The presentstudy was conducted to examine the relationships of leaf waterl, solute s and turgor p potentials, and percent relative watercontent (RWC) of peanut leaves during desiccation of detachedleaves and also during naturally occurring soil moisture deficitsin the field. The relationship of p to l and RWC was evaluated by calculatingp from differences in l and s determined by thermocouple psychrometryand by constructing pressure-volume (P-V) curves from the land RWC measurements. Turgor potentials of Early Bunchand Florunner leaves decreased to zero at l of1.2 to 1.3 MPa and RWC of 87%. There were no cultivardifferences in the l at which p became zero. P-V curves indicatedthat the error of measuring s after freezing due to dilutionof the cellular constituents was small but resulted in artefactualnegative p values. Random measurements on two dates of l, s, and calculation ofp from well-watered and water-stressed field plots consistingof several genotypes indicated that zero p occurred at l of1.6 MPa. It was concluded that the relationships of p,l, s, and RWC of peanut leaves were similar to leaves of othercrops and that these relationships conferred no unique droughtresistance mechanism to peanut. 相似文献
7.
By analysing the relationship between inverse water potential(1), and relative water content (RWC) measured on leavesof roses (Rosa hybrida cv. Sonia), grown soilless, it was foundthat a non-linear (NL) model was better suited than a linearmodel to reproduce values observed in the non-turgid region.To explain this apparent curvature, it is assumed that a reductionof the non-osmotic water fraction (Ap) takes place when decreases.Osmotic potentials () measured on fresh and frozen leaf discstend to support this hypothesis. A method for exploiting PVcurves, which takes into account the variation of Ap, is described.It delivers values for the turgor pressure (p), the relativeosmotic water content, and the mean bulk volumetric elasticitycoefficient, lower than those given by the linear model. Onthe other hand, it gives higher estimates for Ap and for . Whenapplying the traditional model to obtain estimates for waterrelations characteristics of rose leaves, and comparing resultsfrom two distinct salinity treatments (electrical conductivitiesof 1·8 mS cm1 and 3·8 mS cm1, respectively),one deduces a significant reduction of at turgor-loss in thehigh salinity treatment. The NL method is, in addition, ablesimultaneously to reveal a reduction of and a significant increasein p at RWC=100% this proves that soillessgrown roseplants are able to osmoregulate when subjected to a constantand relatively high degree of salinity. Key words: Apoplastic water, non-linear regression, pressure-volume curves, tissue-water relations 相似文献
8.
HENSON I. E.; ALAGARSWAMY G.; MAHALAKSHMI V.; BIDINGER F. R. 《Journal of experimental botany》1983,34(4):442-450
The water potential () at which stomata completed closure (8Lmin)was determined for pearl millet (Pennisetum americanum [L.]Leeke) at two growth stages by monitoring changes in leaf conductance(gL) and following shoot detachment. Leaf water status wasevaluated concurrently using a pressure-volume (P-V) technique. In a pot experiment with young vegetative plants, 8Lmin closelyapproximated to the estimated at zero turgor (u) both for controland for drought-conditioned plants which had osmotically adjusted.However, for penultimate leaves of field-grown flowering plants,8Lmin was found to be 0.61 (irrigated plants) and 0.87 (droughtedplants) MPa below u. In drought-stressed field-grown plants,osmotic adjustment (characterized by a decrease in solute (osmotic)potential (s ) at both full hydration and zero turgor) was insufficientto maintain a positive bulk leaf turgor potential (p) once had declined to below about -1.5 MPa. It is suggested that localizedadjustment by the stomatal complex in response to environmentaldifferences, leaf ageing and/or ontogenetic change, is responsiblefor the uncoupling of stomatal from bulk leaf water status. Key words: Stomata, Water stress, Pennisetum americanum 相似文献
9.
The daily cycle of the transpiration rate, stomatal conductance,water potential, and the concentration of the main osmoticumidentified in ash leaves, malate and mannitol, were monitoredin a field on the Isere river plain. On sunny days, the stomatalconductance tends to remain close to its maximun value allowinga high transpiration rate and diurnal variations in leaf waterpotential, w, which may fall as low as 2 MPa at solarnoon. These variations of w are closely correlated with changesin malate, mannitol and the concentration of the well-knownosmoticum K+, which agree with the involvement of an osmoticadjustment to counteract the evaporative demand during daylighthours. How malate, mannitol and K+ contribute to the osmoticadjustment was analysed subsequently by comparing the solutepotential s, evaluated by the Boyle-Van't Hoff relation, tothe osmotic potential measured by thermocouple psychrometry.These experiments have led us to suspect some errors in themeasurement of , presumably due to experimental artefacts andthe ability of Ca 2+ , present in high levels in leaves, toform chelates with malate once the cells have been decompartmentedby freezing and thawing. Since significant changes of Ca2+ alsooccurred during the diurnal variations of w, the possible mechanismsby which Ca2+ may be implicated in controlling the water statusof the tree are discussed. Key words: Fraxinus excelsior L, osmotic adjustment, thermocouple psychrometry, malate, calcium 相似文献
10.
Legge, N. J. 1985. Water movement from soil to root investigatedthrough simultaneous measurement of soil and stem water potentialin potted trees.J. exp. Bot. 36: 15831589. Osmotic tensiometers implanted in the stems of three mountainash (Eucalyptus regnans F. Muell.) saplings growing in largeplastic bins recorded stem water potential, w, while soil waterpotential, w, was simultaneously recorded by instruments nearthe trees' roots and in the surrounding root-free soil Earlyin a drying cycle, with the soil still wet, the diurnal variationin 1, was often slight, despite diurnal variations in u approaching2.0 M Pa. Late in a drying cycle the diurnal fluctuations in1, and u were very similar although changes in 1, still laggedup to 1.5 h behind changes in u. 1values at this time occasionallyreached 3.0 MPa with no apparent damage to the treesWatering the bins in daytime led to a response in 1, valueswithin about 5 min, whereas u, values did not respond for afurther 20 min. u values then rose rapidly but after only 1h began to decline again, while 1, values remained at or nearsaturation for the rest of the day. Water uptake hypotheseswhich attribute an important role to a soil-root interface resistanceare not supported by these data Key words: Soil water potential, penrhizal gradients 相似文献
11.
The Relationship Between Transpiration Rate, Water Potential, and Resistances to Water Movement in Sunflower (Helianthus annuus L.) 总被引:3,自引:0,他引:3
The effects of transpiration rate on the vertical gradientsof leaf and stem xylem water potential ( and ) were examinedusing hydroponic sunflower plants. Transpiration was variedby stepwise alterations of environmental conditions. The gradientsof and were relatively small (2.3 and 0.8 x 105 Pa m1)when transpiration rates approached zero, but increased sharplyto 5.4 and 2.3 x 105 Pa m1 as transpiration increased.However, the gradients were independent of transpiration ratesabove 0.4 g dm2 h1 owing to variability of theplant resistance. The gradients of I were usually less thanhalf those of I. 1 in individual leaves remained constant over a wide range oftranspiration rates (0.42.4 g dm2 h1) andeach leaf possessed a characteristic plateau value related toits elevation. I responded similarly but was approximately 2.0x 105 Pa higher than I at the same elevation. Identical resultswere obtained regardless of the procedure employed to vary transpiration. The drop in water potential between stem and leaf implies thatthe leaf resistance is appreciable. This was confirmed usingrapidly transpiring excised leaves freely supplied with water.I increased by 2.02.5 x 105 Pa following removal of theroot resistance but remained 2 x 105 Pa lower than similar excisedleaves in darkness. Furthermore, I in excised leaves remainedconstant over a wide range of transporting rates, demonstratingthat the leaf resistance is also variable. The results are discussed in relation to previous reports. 相似文献
12.
An apparatus for determining water potential of leaves () isdescribed. It is a modification of one previously developedby van Andel for determining osmotic potentials of sap (), forwhich purpose it may still be employed. A constantanminalphathermocouple is used for direct determination of wet-bulb temperaturedepression of air in moisture equilibrium with leaves. The system has advantages over others in simplicity of manufactureand electrical circuitry, and in adaptability to a range ofsignal reading and recording methods. It is capable of handlingrelatively large samples, e.g. 20 cereal leaves of total area(single side) of 300 cm2. Tests of leaf maturity and position effects in two potato cropsare described. Differences between corresponding values of and , considered indicative of cell wall pressures, were lessin lower leaves. In one crop, was lower in relation to leafrelative water content with lower than with upper leaves and,in the other crop, with leaves from the more mature stages ofgrowth. These findings are in accord with a higher rigidityof cell walls in lower and more mature leaves. Mean differences of and involved in the above conclusionswere small, usually less than 2 bar, indicating the potentialusefulness of the apparatus. 相似文献
13.
Effects of Priming and Endosperm Integrity on Seed Germination Rates of Tomato Genotypes: II. GERMINATION AT REDUCED WATER POTENTIAL 总被引:3,自引:0,他引:3
Seed germination rates (GR =inverse of time to germination)are sensitive to genetic, environmental, and physiological factors.We have compared the GR of tomato (Lycopersicon esculentum Mill.)seeds of cultivar T5 to those of rapidly germinating L. esculentumgenotypes PI 341988 and PI 120256 over a range of water potential(). The influence of seed priming treatments and removal ofthe endosperm/testa cap enclosing the radicle tip on germinationat reduced were also assessed. Germination time-courses atdifferent 's were analysed according to a model that identifieda base, or minimum, allowing germination of a specific percentage(g) of the seed population (b(g)), and a hydrotime constant(H) indicating the rate of progress toward germination per MPa.h.The distribution of b(g) determined by probit analysis was characterizedby a mean base (b) and the standard deviation in b among seeds(b). The three derived parameters, b, b) and H, were sufficientto predict the time-courses of germination of intact seeds atany . A normalized time-scale for comparing germination responsesto reduced is introduced. The time to germination at any (tg())can be normalized to be equivalent to that observed in water(tg(0)) according to the equation tg(0)=[l(/b(g))]tg().PI 341988 seeds were more tolerant of reduced and had a morerapid GR than T5 seeds due to both a lower b and a smaller H.The rapid germination of PI 120256, on the other hand, couldbe attributed entirely to a smaller H. Seed priming (6 d in1.2 MPa polyethylene glycol 8000 solution at 20 ?C followedby drying) increased GR at all >b(g), but did not lower theminimum allowing germination; i.e. priming reduced H withoutlowering b. Removing the endosperm/testa cap (cut seeds) markedlyincreased GR and lowered the mean required to inhibit germinationby 0.7 to 0.9 MPa. However, this resulted primarily from downwardadjustment in b during the incubation of cut seeds at low inthe test solutions. The difference in b between intact and cutseeds incubated at high was much less (0.l MPa), indicatingthat at the time of radicle protrusion, the endosperm had weakenedto the point where it constituted only a small mechanical barrier.In the intact seed, endosperm weakening and the downward adjustmentin embryo b ceased at < 0.6 MPa, while the reductionin H associated with priming proceeded down to at least 1.2MPa. Based on these data and on the pressure required to pushthe embryos from the seeds at various times after imbibition,it appears that the primary effect of priming was to shortenthe time required for final endosperm weakening to occur. However,as priming increased GR even in cut seeds, priming effects onthe embryo may control the rate of endosperm weakening. Key words: tomato, Lycopersicon esculentum Mill., water potential, germination rate, seed priming, genetic variation 相似文献
14.
Field Studies of Cereal Leaf Growth: IV. WINTER WHEAT LEAF EXTENSION IN RELATION TO TEMPERATURE AND LEAF WATER STATUS 总被引:1,自引:0,他引:1
Throughout winter and early spring, rule and auxanometer measurementsshowed that leaf extension rate (RE) was directly related totemperature and stopped at about 0°C. During this period,both night and day time RE responded similarly to temperature.Bright sunshine in late April and May caused fast transpirationwhich was associated with low leaf water potential () and slowRE. When bright sun was obscured by cloud, RE increased butthis did not compensate for previous slow RE. Leaf turgor potential,calculated as the difference between and leaf osmotic potential,was large (0.61.8 MPa) and bore little relation to RE.Low was associated with slower RE than would have been expectedwithout water stress, but the relation was not unique. On abright day in May, adaptation to low occurred and during theafternoon RE was faster than at similar values of and meristemtemperatures before noon. The response of RE and duration ofleaf extension to temperature suggested that for any particularleaf grown under field conditions, variation in mean growingtemperature would affect final leaf length only slightly. Becausesevere water stress slows RE without affecting the durationof leaf extension markedly, it decreases final leaf size. 相似文献
15.
Water Relations of Potato Leaves. II. Pressure--Volume Analysis and Inferences About the Constancy of the Apoplastic Fraction 总被引:1,自引:0,他引:1
Water relations characteristics of potato (Solanum tuberosumL. cv. Bintje) leaves were determined from pressurevolumeanalysis using a pressure chamber. Turgor was 077 MPa and thebulk volumetric modulus of elasticity 81 MPa at full turgidity;turgor loss occurred when water potential () had declined to087 MPa at a relative water content (RWC) of 0912;the apoplastic water fraction (A) was 0235. As is usually found,there was a linear relation between 1/ and RWC beyond turgorloss. This finding supports the assumptions of the constancyof A during leaf dehydration. Beyond turgor loss the difference between and [measured afterfreezing and thawing (d)] was about 01 MPa. This differencedid not increase as the leaf water content decreased. This resultcontradicts the constancy of A. It was concluded from calculations with a simple model of leafdehydration that analysis of the relation between and d providesmore insight in the changes in the apoplastic fraction thanthe relation between 1/ and RWC. Research on the size of theapoplastic fraction and its changes with water potential wouldcomplement current understanding of leaf water relations. Solanum tuberosum, L., water potential, pressure chamber, osmotic potential, pressure potential, relative water content, apoplast, symplast 相似文献
16.
Field Studies of Cereal Leaf Growth: III. BARLEY LEAF EXTENSION IN RELATION TO TEMPERATURE, IRRADIANCE, AND WATER POTENTIAL 总被引:1,自引:0,他引:1
A mechanical auxanometer, suitable for measuring hourly ratesof leaf extension of grass and cereal crops, is described. Severalof these instruments were used to monitor leaf extension rates(RE) of a spring barley crop. RE of main stem and first leaftillers responded similarly to environmental factors. DuringMay, when soil water deficits were less than 50 mm, and on dulldays later in the season, RE was directly related to meristemtemperature with night and day measurements responding similarly.During the central 10 h of bright days in late May and June,RE was unrelated to temperature but slowed during bright sunshineand accelerated at the start of cloudy periods. Pressure chambermeasurements of total leaf water potential () showed that brightsun caused to decrease rapidly and that this was associatedwith slow RE. Analysis of 2 h mean values of and RE indicatedthat, at any given temperature, RE slowed in direct proportionto decrease of . 相似文献
17.
LARQUE-SAAVEDRA A.; RODRIGUEZ M. T.; TREJO C.; NAVA T. 《Journal of experimental botany》1985,36(11):1787-1792
Larqué-Saavedra, A., Rodriguez, M. T., Trejo, C. andNava, T. 1985. Abscisic acid accumulation and water relationsof four cultivars of Phaseolus vulgaris L. under drought.J.exp. Bot 36: 17871792. Plants of four cultivars of Phaseolus vulgaris L. differingin drought resistance were grown in pots under greenhouse conditionsand prior to flowering water was withheld from the pots untilthe mid-day transpiration rate reached values below 1.0 µgH2O cm2 s1 (designated the droughtstage). At this point leaves were harvested on 3 or 4 occasionsover 24 h to determine the abscisic acid (ABA) concentration,total water potential (), solute potential (1) and turgor potential(p). Results showed that values of , 1, and p differed between cultivarswhen they reached the drought stage. The stomatalsensitivity to changes in and p, was as follows: Michoacán12A3 > Negro 150 Cacahuate 72 > Flor de Mayo. These datacorrelated well with the pattern of drought resistance reportedfor the cultivars. ABA accumulation at the drought stage differedbetween cultivars at each sampling time, but overall differencesin ABA level between cultivars were not significant. ABA levelsdid not, therefore, correlate with the drought resistance propertiesreported for the cultivars. Results are discussed in relationto and hour of the day when bean samples were taken for ABAanalysis. Key words: Phaseolus vulgaris L., drought resistance, abscisic acid 相似文献
18.
Thomas, H. 1987. Physiological responses to drought of Loliumperenne L.: Measurement of, and genetic variation in, waterpotential, solute potential, elasticity and cell hydration.J.exp. Bot. 38: 115125. Clonally-replicated genotypes of Loiium perenne L. were grownin a controlled environment. Leaf water potential (w) osmoticpotential (s), turgor potential (p = w s), elasticity(E), leaf hydration (g water per g dry matter, H) and numberof green leaves per tiller (NGL) were measured before and duringa 42 d drought treatment. A simplified method of estimating E (at w < 1?0 MPa) usingonly six measurements was developed to permit a measurementrate of 8 leaves per hour. Measurement errors in all characterswere 3% or less. During drought, w and s (at w = 0?5 MPa) decreased significantly,p and E increased significantly, and H decreased slightly. Plantsize during drought was negatively correlated with s, and Hand positively correlated with p, osmotic adjustment, E andNGL. Measurements made on the genotypes before draughting didnot give a reliable indication of their physiological conditionafter adaptation to drought. Genetically controlled variation (broad sense heritability)of drought-adapted plants for E was 15%, w 23%, s, 34%, p, 35%,H 34% and NGL 64%. The possibilities for, and effectivenessof, divergent selection of genotypes with high and low expressionof the characters are discussed. Key words: Water relations, Lolium, genetic variation 相似文献
19.
Leaf diffusion resistance interpreted as stomatal resistance,leaf water potential (w), solute potential (s) and leaf turgorpotential (p) of the chilling sensitive species Phaseolus vulgariswere determined during chilling at 4 °C in the light. Bothchill-hardened and non-hardened plants were used. For comparison,the chilling resistant species Pisum sativum was also used. The results for chilled P. sativum were similar to those obtainedfor chill-hardened P. vulgaris plants receiving a chilling treatment.In both cases a reduction in stomatal aperture and the maintenanceof a positive leaf turgor were the responses to chilling. Leavesof chilled but non-hardened P. vulgaris plants were found tomaintain open stomata throughout the chilling treatment despitea severe wilt developing after 7 h at 4 °C. This was incontrast to the chill-resistant P. sativum. which showed a rapidclosing and subsequent re-opening of the stomata to a new reducedaperture. During the first 12 h of chilling wof P. vulgaris leaves changedfrom 0.47 MPa to 1.24 MPa. On more prolonged chillingw tended to return to pre-chilling values. In addition. p decreasedfrom 0.42 MPa to zero after only 9 h of chilling, and remainedat this value for the remainder of the chilling period, s, changedrapidly from 0.89 MPa to 1.35 MPa in the first7.5 h, and after 9 h. w and s, were equal, i.e. zero p. In contrast,the chilling resistant plant P. sativum maintained a positivep throughout the chilling period, and there was little differencebetween values of w, and s in control and chilled leaves. Key words: Chilling, Stomata, ater relations, Phaseolus vulgaris, Pisum sativum 相似文献
20.
Aspects of the water relations of spring wheat (Triticum aestivumL.) are described for cultivars Highbury (low ABA) and TW269/9(high ABA), and low and high ABA accumulating F6selections derivedfrom a cross between them. In a pot experiment, pressure-volume (P-V) curves were constructedfor main stem leaf four (MSL4) of well-watered plants of Highburyand TW269/9. Estimates of solute potential (2) from these curveswere similar for the two cultivars, but varied with the timeof sampling and the time allowed for hydration in dim light. In a field experiment with four low and four high ABA F6lines,P-V curves for flag leaves from both droughted and irrigatedplants gave at both zero turgor (p) and zero water potential(1) which differed with degree of stress, sampling time andgenotype. 1was strongly dependent on the initialL of the leafand was reduced on average by c. 0.4 MPa per MPa decline ininitial L.5, was lower (more negative) by c. 0.1-MPa in theafternoon than in the morning. Overall, was also 0.1 MPa lowerin low ABA lines than in high ABA lines. In another field experiment, flag leaves of five low and fivehigh ABA F6lines were sampled over a 4 week period from droughtedplots and L and 5, measured (the latter by osmometry with expressedsap). For these leaves 5, at zero p or zero L was consistentlylower by 0.30.5 MPa than estimates of 5, from the P-Vcurves with flag leaves. However, data for the low ABA lineswere again lower (by c. 0.1 MPa) than those for high ABA lines. The consequences of these differences in 1 are discussed inrelation to the stimulation of ABA accumulation in low and highABA selections. Key words: Water potential, Solute potential, P-V curves, Wheat (Triticum aestivum), Drought stress 相似文献