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1.
Crop load affects maximum daily trunk shrinkage of plum trees   总被引:1,自引:0,他引:1  
We studied the effects of low fruit load (3-4 fruits cm(-2) of trunk cross-sectional area (TCSA), and high fruit load (6-7 fruits cm(-2) TCSA) on maximum daily trunk shrinkage (MDS) and trunk growth rates (TGR) over two seasons in plum (Prunus salicina Lindell) trees receiving full irrigation or deficit irrigation. Seasonal changes in MDS and TGR were compared with those in midday stem water potential (Psi(s)) and leaf stomatal conductance (g (s)). Crop load increased g (s) in fully irrigated trees approaching harvest. Although crop load did not affect plant water status in either watering regime, there were considerable differences in both MDS and TGR as a function of crop load. Compared with low-cropping [corrected] trees, MDS was 34% higher and TGR was 48% lower in high-cropping [corrected] trees. The differential responses of MDS and Psi(s) to crop load were a consequence of a higher MDS for a given Psi(s) in the high-cropping trees compared with the low-cropping trees. There was a linear increase in MDS with crop load, with a slope of 15.2 microm MPa(-1) per unit increment of crop load. In the fully irrigated trees, day-to-day variations in MDS were related to evaporative demand; however, the slope of the relationship between MDS and evaporative demand increased with crop load, indicating that different reference equations must be used to adjust for tree crop load when using MDS to determine plant water status and irrigation requirements.  相似文献   

2.
Conceptual models accounting for the influence of source:sink ratio on water relations of trees are theoretically relevant from a physiological perspective and practically important for irrigation scheduling. Midday stem water potential of horticultural trees often declines with increasing crop load but the actual response depends on environmental, management and plant factors. Here we advance a quantitative synthesis of the response of stem water potential to crop load from the perspective of phenotypic plasticity, defined as 'the amount by which the expression of individual characteristics of a genotype are changed by different environments'. Data sets of stem water potential for contrasting crop loads were compiled for apple (Malus domestica L. Borkh.), olive (Olea europea L.), peach (Prunus persica L.), pear (Pyrus communis L.) and plum (Prunus domestica L.). Phenotypic plasticity of stem water potential was calculated as the slope of the linear regression between stem water potential for each crop load and the environmental mean of stem water potential across crop loads. Regression lines for trees with different crop load diverged with decreasing environmental mean stem water potential. For the pooled data, plasticity of stem water potential was a linear function of relative crop load. This represents a significant shift in perspective: the effect of crop load on the trait per se (stem water potential) is environmentally contingent, but the effect of crop load on the plasticity of the trait is not. We conclude that research on the effects of crop load on tree water relations would return more robust results if plant traits are considered from the dual perspective of the trait per se and its plasticity.  相似文献   

3.
We studied the relief of water stress associated with fruit thinning in pear (Pyrus communis L.) trees during drought to determine what mechanisms, other than stomatal adjustment, were involved. Combinations of control irrigation (equal to crop water use less effective rainfall) and deficit irrigation (equal to 20% of control irrigation), fruit load (unthinned and thinned to 40 fruits per tree) and root pruning (pruned and unpruned) treatments were applied to pear (cv. 'Conference') trees during Stage II of fruit development. Daily patterns of midday stem water potential (Psi(stem)) and leaf conductance to water vapor (g(l)) of deficit-irrigated trees differed after fruit thinning. In response to fruit thinning, gl progressively declined with water stress until 30 days after fruit thinning and then leveled off, whereas the effects of decreased fruit load on Psi(stem) peaked 30-40 days after fruit thinning and then tended to decline. Soil water depletion was significantly correlated with fruit load during drought. Our results indicate that stomatal adjustment and the resulting soil water conservation were the factors determining the Psi(stem) response to fruit thinning. However, these factors could not explain differences in daily patterns between g(l) and Psi(stem) after fruit thinning. In all cases, effects of root pruning treatments on Psi(stem) in deficit-irrigated trees were transitory (Psi(stem) recovered from root pruning in less than 30 days), but the recovery of Psi(stem) after root pruning was faster in trees with low fruit loads. This behavior is compatible with the concept that the water balance (reflected by Psi(stem) values) was better in trees with low fruit loads compared with unthinned trees, perhaps because more carbon was available for root growth. Thus, a root growth component is hypothesized as a mechanism to explain the bimodal Psi(stem) response to fruit thinning during drought.  相似文献   

4.
A water deficit during stage III of fruit growth was established with the aim of determining if it is possible to achieve an improvement in tree water status by summer pruning and fruit thinning. The experiment was set up as a randomized block split-plot design across trials (irrigation) where pruning was assigned to the main plot and fruit thinning to the sub-plots. The irrigation treatments were (1) standard full irrigation (FI), and (2) suppression of irrigation during stage III of fruit growth until leaves visibly withered (LWI); the pruning treatments were (1) experimental summer pruning (EP), and (2) standard summer pruning (CP); and three fruit thinning intensities were applied to facilitate analysis of the effects of the treatments in relation to fruit load. Changes in amount of light intercepted and in tree stem water potential (Psi stem) were evaluated. The EP treatment reduced the amount of light intercepted by the tree. In the FI treatment, there was a significant reduction in fruit growth measured as both water accumulation and dry mass accumulation. Under FI conditions, reductions in fruit load as a result of EP were not accompanied by a significant improvement in Psi stem. In the LWI treatment, EP produced a significant improvement of 0.17 MPa in Psi stem, but there was no improvement in fruit growth compared with CP trees. A reduction in fruit load from 350 (commercial load) to 150 per tree significantly improved Psi stem by 0.3 MPa at the end of stage III of fruit growth. These results indicate that improvements in water status in response to pruning may be insufficient to promote fruit growth if the pruned trees are unable to provide an adequate supply of assimilates to the developing fruits.  相似文献   

5.
Lopez G  Girona J  Marsal J 《Tree physiology》2007,27(11):1619-1626
Effect of water stress during stage III of peach fruit development on winter root starch concentration (RSC) and subsequent reproductive development was studied. Two irrigation treatments were applied in two consecutive seasons (2003-2004): full irrigation (FI) and no irrigation during stage III of fruit development until visible leaf wilting (LWI), which occurred when midday stem water potential reached -1.80 MPa. Three fruit thinning intensities were applied within each irrigation treatment. The year 2005 was a recovery year in which all trees received full irrigation and commercial fruit thinning. Water deficit and high fruit loads in the previous season significantly reduced the concentration of winter RSC. Fruit set and fruit growth from full bloom to 30 days after full bloom (30 DAFB) increased with increasing winter RSC before other factors, such as inter-fruit competition and availability of carbon from current photosynthesis, came into play. Consequently, severe water stress reduced the total number of fruits and fruit dry mass growth 30 DAFB. However, during the recovery year and after fruit thinning, fruit loads were similar between irrigation treatments and yield capacity remained unaffected. Peach fruit production recovered quickly from the deleterious effects of two consecutive years of water stress because of a combination of two factors: (1) reduced initial fruit set that was still adequate to achieve a commercial crop; and (2) the low sensitivity of fruit growth 30 DAFB to winter RSC.  相似文献   

6.
Four-year-old apple (Malus x domestica Borkh.) trees cv. 'Braeburn' on M.26 rootstock were thinned at full bloom to establish six crop loads ranging from a heavy crop to a deflowered treatment. At harvest, mean yield per tree varied from 0 to 38 kg and mean fruit weight ranged from 225 g in the heaviest cropping treatment to 385 g in the lightest cropping treatment. Light cropping resulted in a significant advance in fruit maturity as indicated by background color, starch/iodine score and soluble solids. There were small differences in leaf photosynthetic rate among the treatments when shoot growth was active. However, in early January, coincident with cessation of shoot growth and maximum rate of accumulation of fruit weight, leaf assimilation rate was reduced by as much as 65% on the deflowered trees compared to the trees carrying the heaviest crop. Leaf assimilation rate showed a curvilinear response to crop load at this time, with little increase in leaf assimilation when crop load exceeded 12 fruit m(-2) leaf area.  相似文献   

7.
In nut tree orchards in California, irrigation is typically withheld during the harvest period to reduce the likelihood of bark damage during mechanical shaking of the trees. The ensuing water stress, however, may result in premature defoliation and subsequent yield declines. Our objective was to establish and quantify the water stress resulting from irrigation deprivation and determine its impact on leaf function and persistence in mature almond trees (Prunus dulcis (Mill.) D.A. Webb cv. Nonpareil) during a 3-year field experiment. The severity of the water stress was characterized by measurements of predawn leaf (Psi(pd)) and midday stem (Psi(ms)) water potentials, stomatal conductance (gs), net CO2 assimilation rate (A) and leaf abscission. During 1995, Psi(ms) of fully irrigated (FI) trees was maintained above -1.0 MPa. In trees in the moderate- (MS) and severe-stress (SS) treatments, Psi(ms) was reduced to -1.4 to -2.0 MPa and -2.0 to -2.6 MPa, respectively. After 18 days of irrigation deprivation, A was reduced by 32 and 58% at midday and early afternoon, respectively, compared with morning values. A significant decrease in morning values of A only occurred after 30 days of irrigation deprivation. Water-use efficiency and A declined as evaporative demand increased from morning to afternoon. Assimilation also declined seasonally as leaves aged. Midday stem water potential was highly correlated with A, but less so with gs. The coefficient of determination between Psi(ms) and gs improved considerably when vapor pressure deficit and wind were multiply regressed with Psi(ms). Although A recovered rapidly when MS trees were irrigated, recovery in SS trees was slower and incomplete. Integrating the MS and SS effects for an extended period during 1995 resulted in 14 and 30% declines in A, and 6 and 20% declines in gs, respectively. The apparent Psi(ms) threshold for leaf abscission was -1.8 MPa. Daily canopy light interception declined with decreasing Psi(ms) as a result of premature defoliation (and perhaps altered leaf angles) from 67.9% in FI trees to 61.4 and 60.7% in MS and SS trees, respectively.  相似文献   

8.
We studied water use by Eucalyptus tereticornis Sm. in two plantations, differing in tree density (1800 stems ha(-1) at Site I and 1090 stems ha(-1) at Site II), in different years. At both sites, stomatal conductance, predawn and midday water potentials and microclimate were measured and used to estimate hourly transpiration by the Penman-Monteith equation. Growth in girth was also measured. Stomatal conductance was closely correlated with atmospheric vapor pressure deficit (D); however, stomata did not close completely even at high D ( approximately 5.0 kPa). Midday leaf water potentials did not fall below -2.0 MPa during any part of the year at either site. Predawn leaf water potentials were greater than -0.25 MPa during the postmonsoon period, but declined to -0.7 MPa at Site I during the premonsoon period. Transpiration estimates ranged from 0.6 to 1.2 mm h(-1) at Site I and from 0.2 to 0.6 mm h(-1) at Site II. The extrapolated transpiration values for the rain-free days of the year were 1563 mm and 853 mm for Sites I and II, respectively. Growth in girth was negligible during the premonsoon period. Photosynthesis was not affected by the minor water stress that developed during the premonsoon period.  相似文献   

9.
Recovery of water status in water-stressed pistachio trees (Pistacia vera L. cv. Kerman) was investigated by subjecting trees to regulated deficit irrigation (RDI) (60% of crop evapotranspiration rate, ET(c)) during stages I and II of fruit development (FD) followed by full irrigation during FD stage III (kernel-filling). Trees irrigated at 100% ET(c) throughout FD stages I, II and III served as controls. Water-stress severity was characterized by changes in soil water content and midday stem water potential (Psi(md)). Midday leaf conductance (g(1)) and trunk diameter variation (TDV) were also measured. In RDI trees, the lowest Psi(md) value, -1.8 MPa, occurred at the end of the RDI period. The corresponding value for the control trees was around -1.1 MPa. Although the RDI treatment affected gas exchange later than Psi(md), the greatest reductions in gas exchange (60% of control values) also appeared at the end of the RDI period. There were significant differences in TDV between control and RDI trees at the end of the RDI period. Although plant water status recovered within 20 days of resuming irrigation, the TDV values indicated a longer period might be necessary for complete recovery. Recovery of g(1) was faster than that of Psi(md), although differences in TDV between control and RDI trees indicated that gas exchange recovered later than Psi(md). The slow recovery of pistachio trees during FD stage III from water stress imposed during FD stages I and II suggests that irrigation should exceed 100% ET(c) during FD stage III or that more extensive irrigation should commence before the end of FD stage II.  相似文献   

10.
This paper offers a different framework for managing Mediterranean drought carob-tree orchard ecosystems. Two dry-farming systems were compared during two consecutive years: pure productive orchards and mixed orchards in a total of 360 mature trees distributed by 18 plots with areas of 0.55 and 0.30 ha per plot, respectively. Carob, fig, almond and olive trees compose mixed orchards. Trees of the mixed orchards were more productive than those of pure orchards. The main problem of both systems was the large variability and the low fruit production due to non-bearing trees, inducing unfavorable economic returns. Yield varied between 7.7 and 28.5 kg tree?1 respectively in pure and mixed orchards. In this paper we propose to use carbon sequestration calculations as an added benefit to farmers. A carbon stocking model estimation was established, based on trunk diameters of different trees. We depicted two management scenarios based on fruits production and carbon sequestration incomes: a low value scenario, using mean fruit production, and a high valuable scenario based on the hypothesis that all trees reached its potential maximum. Since under dry-farming systems fruit production irregularity is still a pendent problem, mixed orchards may offer a potential higher revenue, while maintaining higher crop diversification and whole biodiversity. C sequestration benefit, as here we purpose, may represent 125–300 % of income, respectively under low or high valuable scenario. Thus, CO2 equivalent is a novel ecological economic incentive that may potentiate a new income for farmers while assuring carob ecosystem services.  相似文献   

11.
Effects of irrigation deprivation during the harvest period on yield determinants in mature almond (Prunus dulcis (Mill.) D.A. Webb cv. Nonpareil) trees were investigated during a 3-year field experiment. Return bloom and fruit set were measured on 2185 individually tagged spurs. Water stress resulting from irrigation deprivation during the harvest period, which purportedly coincides with the time of flower initiation, had no effect on the percentage of spurs that flowered or set fruit during subsequent years. Although water stress had no apparent effect on spur mortality, 66% of the tagged spurs died within 3 years. In addition, many spurs were vegetative by the third year, indicating the importance of spur renewal for sustained fruit production. Reductions in nut yield were evident after two successive years of irrigation deprivation during the harvest period. Regression analysis indicated a loss in yield of 7.7 kg tree(-1) in response to each 1 MPa decrease in stem water potential below -1.2 MPa during the previous seasons. The number of fruiting positions per tree (estimated indirectly for whole trees based on weight of current-year shoots > 5 cm in length) was negatively associated with water stress. Yield reduction in response to water stress during harvest appears to be a compound, multiyear effect, associated with reduced annual growth and renewal of fruiting positions.  相似文献   

12.
Environmentally sound management of N in apple orchards requires that N supply meets demand. In 1997, newly planted apple trees (Malus domestica Borkh. var. Golden Delicious on M.9 rootstock) received daily applications of N for six weeks as Ca(15NO3)(2) through a drip irrigation system at a concentration of 112 mg l(-1) at 2-8, 5-11 or 8-14 weeks after planting. Irrigation water was applied either to meet estimated evaporative demand or at a fixed rate. In 1997, trees were harvested at 5, 8, 11 and 14 weeks after planting; and in 1998 at 3 weeks after full bloom. The amount of fertilizer N recovered was similar in trees in both irrigation treatments, but efficiency of fertilizer use was greater for trees receiving demand-controlled irrigation than fixed-rate irrigation. This was attributed to lower N inputs, greater retention time in the root zone and less N leaching in the demand-controlled irrigation treatments compared with fixed-rate irrigation treatments. Less fertilizer N was recovered by trees receiving an early application of N than a later application of N and this was related to the timing of N supply with respect to tree demand. Demand for root-supplied N was low until 11 weeks after planting, because early shoot and root growth was supported by N remobilized from woody tissue, which involved 55% of the total tree N content at planting. Rapid development of roots > 1 mm in diameter occurred between 11 and 14 weeks after planting, after remobilization ended, and was greater for trees receiving an early application of N than for trees receiving a later application of N. Late-season tree N demand was supplied by native soil N, and uptake and background soil solution N concentrations were higher for trees receiving demand-supplied irrigation compared with fixed-rate irrigation. Total annual N uptake by roots was unaffected by treatments and averaged 6-8 g tree(-1). Nitrogen applications in 1997 affected growth and N partitioning in 1998. Trees receiving early applications of N had more flowers, spur leaves and bourse shoots than trees receiving later applications of N. Consequently, more N was remobilized into fruits in trees receiving early applications of N compared with fruits in trees receiving later applications of N. Demand for N in the young apple trees was low. Early season demand was met by remobilization from woody tissues and the timing of demand for root-supplied N probably depends on whether flowering occurs. Method of N delivery affected the efficiency of N use. We conclude that N demand can be met at soil solution N concentrations of around 20 mg l(-1).  相似文献   

13.
We investigated crop load and water stress effects on diurnal stem extension growth of field-grown peach (Prunus persica (L.) Batsch) trees. Neither the presence of fruit nor reduced irrigation significantly altered the timing of diurnal fluctuations in stem growth rate. Stems with subtending fruit had significantly reduced growth compared to stems with no subtending fruit. Crop load had no significant effect on relative stem extension rates and the majority of the reduction in absolute growth was the result of a smaller zone of elongation in fruit-bearing stems than in stems with no subtending fruit. Fruit removal did not increase growth rates within 24 h. When irrigation was reduced, the length of the stem elongation zone and total daily stem growth were significantly decreased relative to well-irrigated controls and the decreases were highly correlated with stem water potential. Compared with well-irrigated controls, relative stem extension rates of water-stressed trees were reduced at several times during the 24-h period, but the degree of reduction was not proportional to the difference in stem water potentials between the treatments.  相似文献   

14.
Net photosynthetic rates (A) of leaves on 11-year-old, field-grown apple trees (Malus domestica Borkh. cv. Golden Delicious) were measured after removal of fruits at four different stages of development. Defruiting decreased A by 21, 42, 27 and 7% when fruits were growing at 311, 293, 229 and 113 mg(DW) day(-1), respectively. Photosynthesis was inhibited more in the afternoon than in the morning, but it was not affected during the first 8 h after fruit removal. Inhibition of A was positively correlated with crop sink strength, but it was not correlated with fruit relative growth rate or crop load. Defruiting decreased A at saturating irradiances (PPFD > 1000 micro mol m(-2) s(-1)), but did not modify the apparent quantum yield of single leaves. These results suggest that the overall effect of defruiting on carbon fixation is negligible in dense canopies, but it may be significant in sparse canopies and in single shoots.  相似文献   

15.
Berman ME  DeJong TM 《Tree physiology》1996,16(10):859-864
Effects of water stress on fruit fresh and dry weights were investigated in peach trees, Prunus persica (L.) Batsch., with varying crop loads: light, moderate and heavy. In well-watered controls, tree water status was independent of crop load. In trees receiving reduced irrigation, the degree of water stress increased with increasing crop load. Water stress induced fruit fresh weight reductions at all crop loads. Fruit dry weight was not reduced by water stress in trees having light to moderate crop loads, indicating that the degree of water stress imposed did not affect the dry weight sink strength of fruit. Water-stressed trees with heavy crop loads had significantly reduced fruit dry weights, which were likely due to carbohydrate source limitations resulting from large crop carbon demands and water stress limitations on photosynthesis.  相似文献   

16.
Between June 1993 and June 1994, 112 farmers in the oil palm (Elaeis guineensis)-cassava (Manihot esclentus) belt of southeastern Nigeria were interviewed to determine the status and agroforestry potential of Dacryodes edulis. Between 50% and 100% of respondents in different states within the belt owned D. edulis trees. On average, a farmer owned 9.3 trees, the largest number being 16, by farmers in Imo State. Twenty percent of farmers in the system rated D. edulis their best farm tree. It was present in all the farm niches: homegardens (51.4%), tree crop plots (20.7%) food crop plots (11.4%), secondary forest/fallow (14.2%) and virgin forest (2.5%). The tree is planted primarily for home consumption and sale to generate cash. At the current densities, on-farm D. edulis trees generally did not decrease yield of companion crops or trees. Except for ring weeding around the stem, D. edulis trees received little or no management attention. More than 50% of the trees produced 33 to 50 kg of fruit tree−1 annually. This is valued at US $0.4 to 0.8 kg−1. Farmers were willing to plant more D. edulis trees provided trees with traits such as less height for easy harvesting of fruits, larger fruit, more fruits, sweeter fruits and year round production of fruits were available. Possible agroforestry technologies into which D. edulis may fit include live fences, scattered trees in food crop fields, shade trees in tree crop plots and contour bund or hedgerow planting. Research is required to determine best tree accessions, canopy management strategies, optimum tree population and improved methods on post- harvest handling of fruits. This revised version was published online in June 2006 with corrections to the Cover Date.  相似文献   

17.
苹果树梨树腐烂病是对果树危害严重的一种病害,对果树生产造成了较大的威胁。通过对苹果树梨树腐烂病发生程度的相关性因素的分析,结果表明,苹果树梨树腐烂病的发生程度与果树大小年、树龄、果树生长状况、冻害的发生、土壤管理制度、修剪程度等都有十分密切的相关性:树龄1~10a的发病轻,20a以上的发病重;枝条发育不充实,不能自然落叶的果园发病重,枝条充分成熟的树体发病轻;易遭冻害的果园发病重;清耕不间作的果园发病重,间作的发病轻;重修剪的发病重,轻修剪的发病轻。  相似文献   

18.
为探明山旱塬区苹果园耗水规律以及影响果树耗水的主导因子,确定水分承载力,合理配置有限的水资源,于2014~2015年采用SF-L树干茎流仪和Watch Dog 2900ET自动气象站对山旱塬区花牛苹果树干茎流及环境因子进行了连续观测,分析了花牛苹果树干茎流速率的变化规律及其与环境因子的相关关系。结果表明,在果树生长周期,各月份根据日均茎流速率由大到小排列依次为5月、6月、7月、8月、9月,随着月份的递增,茎流峰值出现时间逐渐延迟;5~9月份苹果树干茎流速率变化规律表现为昼高夜低,7:00~9:00树干茎流速率开始急速上升,12:00~15:00达到最大值,17:00~18:00开始逐步下降,21:00趋于稳定;不同天气条件下苹果树干茎流速率为晴天大于雨天;对茎流速率与环境因子的相关性分析结果表明,太阳辐射强度、相对湿度、空气温度、饱和水气压差、露点温度与树干茎流速率呈极显著性相关,风速对茎流速率也有一定影响。  相似文献   

19.
Surface conductance to water vapor diffusion was measured in individual peach fruits (Prunus persica (L.) Batsch) and plotted as a function of fresh fruit mass for four cultivars. Surface conductance increased with fresh fruit mass, but the pattern differed with cultivar, and fruit-to-fruit variation occurred. Relationships between fruit mass and surface conductance were modeled by fitting mathematical equations to the data. The simulation model of Fishman and Génard (1998) was used to study dry mass and water components of fruit growth (1) when surface conductance varied with fruit size or was constant, and (2) when surface conductance values were high, moderate or low with respect to fruit mass. Increased surface conductance with fresh fruit mass resulted in fruit growth cessation. Fruits differing in surface conductance had similar dry mass. However, under well-watered conditions (stem water potential between -1 and -0.2 MPa), the water balance components of growth (osmotic and hydrostatic pressure, water potential and water balance) differed greatly and, as a result, the lower the surface conductance the greater the fresh fruit mass. These differences were buffered under drought conditions (stem water potential between -2.4 and -0.6 MPa).  相似文献   

20.
Five-year-old early maturing peach trees (Prunus persica (L.) Batsch cv. Flordastar grafted on GF-677 peach rootstock) were subjected to three irrigation treatments from March 18 to November 10, 2006. Control plants (T0 treatment) which received irrigation in excess of their crop water requirements (1089.7 mm) were compared with plants watered according to sap flow (SF; T1 treatment) or maximum daily trunk shrinkage (MDS; T2 treatment) measurements, so as to maintain SF and MDS signal intensities (control SF/SF in T1 and MDS in T2/control MDS, respectively) close to unity. When SF or MDS signal intensity on at least two of three consecutive days was at or below unity, irrigation was reduced by 10%. When the MDS signal intensity on at least two of three consecutive days exceeded unity, irrigation was increased by 10%. During the experiment, estimated crop evapotranspiration was 704.9 mm, and the cumulative amounts of applied water in the T1 and T2 treatments were 463.2 and 654.5 mm, respectively. The MDS-signal-intensity-driven irrigation schedule was more suitable than the SF-signal-intensity-driven irrigation schedule because it was more sensitive and reliable in detecting changes in plant water status, preventing the development of detectable plant water stress. Moreover, it had no effect on fruit size. We conclude that peach tree irrigation scheduling can be based on MDS measurements alone. Changes in the irrigation protocol assayed were proposed to reduce MDS signal intensity deviations above unity, for example, by increasing the irrigation scheduling frequency or the amount of water applied, or both. Irrigation schedules based on maintaining MDS signal intensities close to unity could be applied when local crop factor values are unavailable.  相似文献   

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