Effect of soil water osmotic potential on growth and water relationships in barley during soil water depletion

Summary Barley plants (Hordeum distichum, L., cv. Zita) grown in a sandy soil in pots were adjusted during a pretreatment period of 5 days to three levels of soil water osmotic potential by percolating 61 of a nutrient solution with additional 0, 22.3 and 44.6 mM KCl. A drying cycle was then started and the plants were harvested when the soil water matric potential had decreased to –1.4 MPa, respectively 6, 7 and 8 days later.No significant differences in dry matter yields, transpiration coefficients and wilting percentages were found between treatments.During the drying cycle leaf water potential ( _l ) decreased concomitantly with decrease in soil water potential ( _s ) with almost constant and similar differences ( _l – _s ) for all treatments despite differences in levels of potentials. The concomitant decrease in leaf osmotic potential () was due partly to dehydration (58%) and partly to increase in leaf solute content (42%) independent of treatment. The part of total osmotic solutes due to K decreased relatively during the drying cycle.Close relationships were found between and _l as functions of relative water content (RWC). Identical curves for the two levels of salt treatment agree with similar concentrations of K, Cl, and ash found for salt treated plants indicating that maximum uptake of macro nutrients may have been reached.During the main part of the drying cycle the turgor potential as function of RWC was higher and decreased less steeply with decreasing RWC in the salt treated than in the non-salt treated plants.In the beginning of the drying cycle additions of KCI lowered the transpiration rates of the salt treated plants resulting in a slower desiccation of the soil and hence an increased growth period. A delay in uptake from a limited soil water supply may be advantageous during intermittent periods of drought.     

Pressure chamber procedures for leaf water potential measurements of cotton

Summary Measurement of leaf water potential ( _l ) with a pressure chamber is usually regarded as a reliable and practical field technique. However, recent evidence indicates that results depend on the measurement techniques employed. Field experiments were conducted to identify the magnitude and sources of error affecting pressure chamber measurements of _l in cotton (Gossypium hirsutum L.) and to develop an accurate and operationally flexible procedure. Water potential of bare cotton leaves was about 0.2 MPa less than aluminum foil wrapped leaves when the elapsed time between excision to chamber pressurization was less than 30 s. The water potential of intact leaves increased 0.3 MPa after 15 s of enclosure in aluminum foil. 5 to 30 min of enclosure were sufficient to reach equilibrium between _l and water potential within the plant stem. Aluminum foil wrapped leaves maintained their _l for 2 h stored in a humid, dark box at 21–28 °C while wet wrapped (cheesecloth) or bare leaf _l increased after one hour because of hydration. An accurate and operationally flexible _l measurement procedure, suitable for large scale sampling, was defined.Contribution from the USDA-ARS, Water Management Research Laboratory, 2021 S. Peach, Fresno, CA 93727 and the Dept. of Land, Air and Water Resources, University of California, Davis, CA 95616, USA     

Establishment of shallow and restricted root systems in cotton and its impact on plant response to irrigation

Summary The effects of frequent and shallow soil wetting by surface drip irrigation on root growth, morphology, and location, and their impact on plant sensitivity to irrigation management were studied in cotton (Gossypium hirsutum L.). Daily drip irrigation, which wetted the 0 to 40-cm soil depth, encouraged root development mainly around the drippers. Water extraction took place mostly from 0 to 20 cm below the drippers, where the roots were concentrated. Shallowness of root growth was not altered by the expansion and deepening of the wetted soil zone which resulted from an increase in amount of irrigation water. The shallow and restricted root system was characterized by a high fraction of thin roots (less than 1 mm dia.) which comprised almost 90% of the root dry matter. Root proximity to the drippers and the limited amount of water in the rooted soil led to a sensitive and quick response of the plants to small amounts of irrigation. A supply of 1.0 mm H₂O given at midday to 70 day-old plants resulted in a leaf water potential (L _w) increase from –1.64 to –1.32 MPa over a 20-min period. This amount of irrigation comprised 15% of the average daily quantity. A 24 h delay in irrigation to 80 dayold plants was enough to decrease L _w from –1.41 to –2.42 MPa. This decrease was caused by a soil water deficit of less than 6 mm H₂O. Extending the irrigation delay to 72 h affected yield and earliness, although the deficient amount of water was supplied over the several days after the treatment. A strong response to minor, but continuous, differences in the daily irrigation amount was detected. Differences in irrigation of less than 1 mm H₂O per day applied during the whole growth season substantially affected L _w, yield and earliness. It was concluded that the establishment of a shallow and restricted root system resulted in strong dependence of the plants on frequent and sufficient supply of water, and temporary minor changes in irrigation affected plant water status and productivity.     

Response of cotton water stress indicators to soil salinity

Summary A field study was conducted on cotton (Gossypium hirsutum L. c.v. Acala SJ-2) to investigate the effects of soil salinity on the responses of stress indices derived from canopy temperature, leaf diffusion resistance and leaf water potential. The four salinity treatments used in this study were obtained by mixtures of aqueduct and well water to provide mean soil water electrical conductivities of 17, 27, 32 and 38 dS/m in the upper 0.6 m of soil profile. The study was conducted on a sandy loam saline-alkali soil in the lower San Joaquin Valley of California on 30 July 1981, when the soil profile was adequately irrigated to remove any interference of soil matric potential on the stress measurements. Measurements of canopy temperature, leaf water potential and leaf diffusion resistance were made hourly throughout the day.Crop water stress index (CWSI) estimates derived from canopy temperature measurements in the least saline treatment had values similar to those found for cotton grown under minimum salinity profiles. Throughout the course of the day the treatments affected CWSI values with the maximum differences occurring in mid-afternoon. Salinity induced differences were also evident in the leaf diffusion resistance and leaf water potential measurements. Vapor pressure deficit was found to indicate the evaporative demand at which cotton could maintain potential water use for the various soil salinity levels studied. At vapor pressure deficits greater than 5 kPa, cotton would appear stressed at in situ soil water electrical conductivities exceeding 15 dS/m. The CWSI was as sensitive to osmotic stress as other, more traditional plant measures, provided a broader spatial resolution and appeared to be a practical tool for assessing osmotic stress occurring within irrigated cotton fields.     

Relationships between crop temperature,grain yield,evapotranspiration and phenological development in two hybrids of moisture stressed sorghum

Summary Recent studies have shown that the grain yields of corn (Zea mays L.) and wheat (Triticum aestivum L.) are related to the degree of water stress they undergo. The purpose of the study reported here was to establish relationships between crop temperature and the grain yields, phenological development, evapotranspiration rates (ET) and leaf water potential ( _l ) of two hybrids of grain sorghum (Sorghum bicolor L. Moench) subjected to varying levels of plant water stress. The study was conducted at the University of Nebraska Sandhills Agricultural Laboratory in 1978 on a Typic Ustipsamment (Valentine fine sand) soil. The sorghum hybrids used were RS 626 and NB 505. Four irrigation treatments were applied in order to subject the crops to varying levels of water stress during each of three major growth stages. Soil moisture was monitored with a neutron probe. ET was estimated with the water balance technique. Crop temperature was measured with an IR thermometer and leaf water potential was measured with a Scholander pressure bomb. Grain yields were reduced by water stress occuring at anytime during the growing season. Yield reductions were largest when stress occurred during only the grainfill period and were least when stress occurred during the entire growing season. The percentage reduction in sorghum grain yield can be described by an index involving the seasonal accumulation of the daily mid-day temperature differences between well-watered and stressed crops ( TSD). As TSD values increased, ET decreased. However, the correlation of ET with TSD was relatively low (R² = 0.60) probably due to the limited amount of data available for analysis and inaccuracies in the soil water balance method used to estimate ET. The mid-day temperature of well-watered rows ranged between 18.0 and 32.8 °C with a mid-day temperature range of about 0.5 °C between the well-watered rows in various plots for several days following an irrigation. However, in certain instances, the mid-day temperature range increased to 1–2 °C for a few days before irrigation. This suggests that certain of the rows experienced water stress and should have been irrigated earlier. Yield data support that conclusion. Range in crop temperature within a field appeared to be a sensitive indicator of crop water stress in sorghum. No significant difference in the phenological development of sorghum resulted from water stress except in one NB 505 plot in which plants were stressed throughout the entire season. In that plot, the stressed plants lagged in development behind non-stressed plants by approximately ten days. The differences in mid-day leaf water potentials ( _l ) and crop temperatures (T) between stressed and non-stressed vegetation were examined. As T increased up to about 4 °C, _l , also increased. Beyond that point, _l decreased while T continued to increase. This behavior was attributed to stomatal closure which permitted an increase in _l of the stressed plants (hence reducing _l ) even as T continued to increase.Published as Paper No. 6551, Journal Series, Nebraska Agricultural Experiment Station. The work reported was conducted under Regional Research Project 11–33 and Nebraska Agricultural Experiment Station Project 11–50. The work upon which this publication is based was supported in part by funds provided by the Office of Water Research and Technology B-044-NEB, US Department of the Interior, Washington, DC, as authorized by the Water Research and Development Act of 1978. This article was sponsored in part by the Nebraska Water Resources Center, Institute of Agriculture and Natural Resources, University of Nebraska-LincolnResearch Assistant, Associate Professor, Research Assistant, and Associate Professor, University of Nebraska, Lincoln. Contents of this puplication do not necessarily reflect the views and policies of the Office of Water Research and Technology, US Dept. of the Interior, nor does mention of trade names or commercial products constitute their endorsement or recommendation for use by the United States Government     

Effect of root and water distribution in lysimeters and in the field on the onset of crop water stress

Summary Lysimeters have been frequently used to study crop response to the onset of water stress. To test the representativeness of lysimeter derived criteria for the onset of crop water stress, spring wheat (Triticum aestivum L.) was grown in two field plots with 1.0 m deep lysimeters in the center of each plot. One plot was well-watered while the second was subjected to a drying period with no irrigation. Crop water stress was assessed by monitoring leaf water potential ( _l ), stomatal diffusive resistance (r _s ), canopy temperature (CT), evapotranspiration (ET), and soil water content in both plots and lysimeters. The rate of change of all these measured parameters, when compared to the well-watered field control-plot revealed that the field-grown plants showed signs of water stress long before the lysimeter-grown plants. Water stress developed gradually for the field crop, but the transition from the well-watered to the stressed condition happened abruptly for the lysimeter-grown plants. Once this transition occurred, the lysimeter-grown plants were more drought stressed than the field-grown plant. Water profiles measured inside the lysimeter were different from those measured in the adjacent plots. An increase in root length density with depths below 0.6 m was observed in the lysimeters as opposed to a quasimonotonic decrease with depth in the field. The response of the lysimeter-grown plants was a result of the anomalous water content and root distribution. We conclude that threshold values of ET, _l , r _s , and CT for the onset of water stress obtained when deep-rooted crops grown in a shallow lysimeter are subjected to drought periods may not be directly applicable to field situations.     

Irrigation scheduling in a mature peach orchard using tensiometers and dendrometers

Three trickle irrigation schedules, two of which were scheduled according to soil water potential ( soil) (tensiometer method) and daily stem contraction (DSC) (dendrometer method) respectively and the other one was a schedule of restricted water supply, were applied to a mature peach orchard.The annual water application based on soil was greater than that based on DSC. However, tree growth, fruit size and leaf water potential (leaf) on the trees in the dendrometer scheduling plot did not differ from those in the tensiometer scheduling plot while the premature fruit drop and fruit bud initiation were greatly different. The restricted water supply treatment limited significantly both tree and fruit growth. In addition, the lower leaf was observed on the trees in this plot.Further study shows that use of the dendrometer method for scheduling irrigation satisfies the water needs of the plant and that the tensiometer method is less accurate.Abbreviations leaf leaf water potential - soil soil water potential - DSC daily stem contraction - LVDT linear variable displacement transducer - PET potential evapotranspiration     

Continuous measurement of plant and soil water status for irrigation scheduling in plum

The usefulness of continuous measurement of soil and plant water status for automated irrigation scheduling was studied in a drip-irrigation experiment on plum (Prunus salicina Black Gold). Two levels of water restriction were imposed at different phenological periods (from pit-hardening to harvest, post-harvest) and compared with a well irrigated control treatment. Soil matrix water potential (_soil) was measured with granular matrix sensors (Watermark); and short-period trunk diameter variation (TDV) was measured with linear variable displacement transformers. The Watermark sensor readings were in reasonable agreement with the irrigation regime and showed a good indication of plant water status across the season (r²=0.62), although they were a better predictor of stem water potential (_stem) in the dry range of _soil. Nonetheless, the most important drawback in their use was the high variability of readings (typical CV of 35–50%). From TDV measurements, maximum daily shrinkage (MDS) and trunk growth rate (TGR) were calculated. Their performance was also compared with _stem, which had the lowest variability (CV of 7%). During most of the fruit growth period, when TGR was minimum, MDS was higher in the less-irrigated treatment than in the control and correlated well (r²=0.89) with _stem. However, after harvest, when TGR was higher, this correlation decreased as the season progressed (r²=0.73–0.52), as did the slope between MDS and _stem, suggesting tissue elasticity changes. Later in the season, TGR was better related to plant water status. These observations indicate some of the difficulties in obtaining reference values useful for irrigation scheduling based exclusively on plant water status measurements.     

Effects of frequency of irrigation and gypsum treatment on leaf water potential and leaf stomatal conductance of lucerne (Medicago sativa L.) grown on a heavy clay soil

Summary Concurrent diurnal measurements of water potential, osmotic potential and conductance were made on leaves of lucerne grown under weekly (W) and fortnightly (F) irrigation on gypsum-treated (G) and untreated soil (C). Measurements were made throughout the period of vegetative growth.Leaf water potentials were lower both at dawn and in the afternoon under fortnightly as compared to weekly irrigation. Gypsum application led to a slower decline in water potential under fortnightly irrigation, although the effect was small compared with more frequent irrigation. Stomatal conductance was reduced under treatments F_G and F_C during the later stages of vegetative growth, coinciding with leaf water potentials of less than c. –1.6 MPa.The relationship between leaf water potential and turgor potential changed with time such that positive turgor was maintained as leaf water potential declined. Turgor maintenance was achieved through a decrease in leaf osmotic potential. These data suggest that lucerne is capable of osmotic adjustment.Stomatal conductance declined rapidly below a leaf turgor potential of c. 0.1 MPa. It is hypothesised that osmotic adjustment enabled stomatal adjustment, which contributed to continued assimilation despite increasing soil moisture deficits.     

Cotton root and shoot responses to subsurface drip irrigation and partial wetting of the upper soil profile

The ability of cotton roots to grow downwards through a partially-wetted soil (Calcic Haploxeralf) profile toward a water source located beneath them was investigated. Plants were grown in 60-cm-high soil columms (diameter 10 cm), the bottom 15 cm of which was kept wet by frequent drip irrigation, while the upper 45 cm was wetted three times per week up to 20, 40, 60, 80 or 100% of pot capacity. Pot capacity was defined as the water content which gave uniform distribution within the pot and was at a soil matric potential ( _m ) of –0.01 MPa. Plants were harvested 42 and 70 days after emergence (DAE). Root length density was reduced by decreased soil moisture content. At 42 DAE, density was reduced in the soil profile down to 36 cm. The density in the middle segment of the cylinder (24–36 cm) increased at the second harvest, from 0.1 to 0.35 cm · cm^–3 at 40% and from 0.2 to 0.5 cm · cm^–1 at 60% of pot capacity, respectively. A significant rise in root length density was found at all moisture contents above 20% in the two deepest soil segments. It was most marked at 40% where the rise was from 0.2 to 0.8 cm · cm^–3, due to the development of secondary roots at the wetted bottom of the column. When only 20% of pot capacity was maintained in the top 45 cm of the profile, almost no roots reached the wetted soil volume, and root length density was very low. Hydrotropism, namely root growth through dry soil layers toward a wet soil layer was thus not apparent. Root dry weight per unit length decreased with increasing depth in the column at all moisture levels. However, the only significant decrease was, found between the top and the second soil segments and was due to thicker primary roots in the top segment. There was no clear relationship between length and dry weight of roots. Total plant dry weight and transpiration were reduced significantly only at 20% of pot capacity. Dry matter production by roots was less severely inhibited than that by shoots, under decreased moisture content in the soil profile. Leaf water potential decreased when the soil moisture content of the top 45 cm of the profile was reduced below 60% of pot capacity. It was concluded that even at soil moisture content equivalent to a _m of 0.1 MPa, the rate of root growth was sufficient to reach a wetted soil layer at the bottom of the soil column, where the plant roots then proliferated. This implies that as long as the soil above the subsurface dripper is not very dry there is no real need for early surface irrigation.     

Comparing deep drainage estimated with transient and steady state assumptions in irrigated vertisols

Chloride mass balance (steady state or transient state) models are used extensively in Vertisols of Queensland and New South Wales (NSW) in Australia to estimate deep drainage. The aim of this study was to compare deep drainage estimated assuming steady state and transient state conditions with chloride mass balance models in irrigated cotton (Gossypium hirsutum L.)-based farming systems in the lower Namoi Valley of North Western NSW. Drainage was estimated at seven sites, and treatments included rotation crops such as wheat (21–62 mm/year) (Triticum aestivum), sorghum (12–47 mm/year) (Sorghum bicolor) and dolichos (12–21 mm/year) (Lablab purpureus), minimum tillage (62–83 mm/year), where cotton was sown into standing wheat stubble, and conventional tillage where stubble was incorporated (35–78 mm/year). Soil water content was measured with a neutron moisture meter in the 0.2–1.2 m depth. Soil was sampled before sowing and after harvest to a depth of 1.2 m along diagonal transects. The soil chloride concentration was determined by titration with AgNO₃. Irrigation water was also analysed for chloride. The deep drainage estimates were compared using regression analysis and students paired t-test. In addition, a paired t-test of the soil chloride concentration before sowing and after harvest was used to determine if the soil chloride flux was either in a steady state or transient state. In 9 out of the 13 data sets (69%), drainage estimated with the models agreed with changes between pre- and post-season soil chloride concentrations. Under frequently irrigated summer crops such as cotton and sorghum and in better structured soils chloride flux reached steady state conditions whereas under partially-irrigated crops or where soil structure was poorer, the chloride flux deviated markedly from steady-state conditions. The latter observation may be due to preferential flow via deep cracks in infrequently irrigated soil. Deep cracking would be due to the more intense shrinking and swelling in partially irrigated soil in comparison with frequently-irrigated crops. Comparison of estimated deep drainage with pre- and post-season soil chloride concentrations showed that the steady state mass balance model best estimated deep drainage under cotton crops which were irrigated more frequently or wheat crops which had better soil structure.

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Canopy temperature and water stress of cotton crops with complete and partial ground cover

Summary The use of canopy and air temperature differences to compute a crop water stress index (CWSI) for assessing plant water status was investigated using cotton crop canopies that either fully or partially covered the ground. The complete ground cover canopy condition was studied in a well watered moisture regime in a rainout shelter with measurements made on six Texas cotton race stocks. The partial ground cover canopy situation was investigated in a well watered moisture regime of a commercial cotton variety Paymaster 266 grown in the field. The slope of the nonstressed baseline of the CWSI for a cotton canopy with about 50% ground cover was approximately one-half that reported for full canopies. Values of CWSI calculated with theoretical and empirical procedures agreed more closely under a complete canopy condition than under a partial canopy situation. Values of aerodynamic resistance (r _a ) and canopy resistance for well watered soil moisture conditions (r _ep )were estimated in order to use the theoretical procedure of computing CWSI. Values of r _a ranged from 10 to 15 sm^–1 and r _cp from 50 to 60 sm^–1. Both the theoretical and empirical procedures showed much promise, but more information is needed to develop techniques for evaluating r _a and r _cp under differing canopy and environmental conditions.     

Drought sensitivity,root development and osmotic adjustment in field grown peas

Summary In order to study the drought sensitivity of pea (Pisum sativum L. cv. Bodil) during different growth phases, a field experiment was conducted in 1985 and 1986 on coarse textured sandy soil with low water-holding capacity. Drought occurred naturally or was imposed by shelters during the vegetative, the flowering and the pod filling growth phase, respectively. Drought sensitivities were assessed as the ratio between relative yield decrease (1 – Y_a/Y_m) and relative evapotranspiration deficit (1 – ET_a/ET_m) of the individual growth phases, where Y_a and ET_a are the actual yield and evapotranspiration, respectively, of a drought stressed plot and Y_m and ET_m are the maximum yield and evapotranspiration of the fully irrigated treatment. Root growth was followed by measuring root density (L _v ) in 10 cm soil layers to a depth of 50 cm. The leaf osmotic potential at full hydration ( _s ¹⁰⁰ ) was measured in the last fully developed leaf during the growing season.The available water capacity was estimated to be 42–50 mm on the basis of a plot of ET_a/ET_m versus soil water deficit measured by the neutron moderation method or direct measurement of the root depth. The root zone with L _v >0.1 cm^–2 only reached a depth of 35 cm at the end of the flowering phase and a depth of 45–50 cm at maturity. Root growth continued during the drought periods. The drought sensitivity of pea was high during the flowering phase, especially in 1986 when water stress developed rapidly, and considerably lower during the pod filling phase. The yield reduction caused by drought in the flowering phase was mainly the result of a lower number of pods per stalk. Severe drought did not occur during the vegetative phase. The leaf osmotic potential ( _s ¹⁰⁰ ) declined from c. -0.75 MPa to c. -1.30 MPa during the growing season. Osmotic adjustment was largest during drought in the early growth phases; in 1985 _s ¹⁰⁰ decreased 0.5 MPa under relatively slow drought development during the flowering phase while in 1986, when drought stress developed rapidly, _s ¹⁰⁰ only decreased 0.2 MPa. Osmotic adjustment may have caused the lower drought sensitivity in 1985 than in 1986 and mediated the continued root growth during drought.     

Water relations of drought-resistant and drought-sensitive wheat cultivars sprinkled with saline water

Summary Water potential, osmotic potential, turgor potential, and stomatal resistance were measured on leaves of a drought-sensitive (Ponca) and a drought-resistant (KanKing) cultivar of winter wheat (Triticum aestivum L.) treated with foliar applications of NaCl to determine the effect of salt on the water status of two cultivars varying in drought resistance. Plants were grown under controlled conditions in soil, which was watered or allowed to dry. Water potential of the soil was determined. Given an ample water supply, water potential and osmotic potential of leaves of both cultivars with NaCl were lower, and stomatal resistance was higher, than without NaCl. The combination of salt and drought killed both cultivars, but the turgor potential of the drought-sensitive cultivar with the two stresses reached zero before that of the drought-resistant cultivar. Under limited water supply, both cultivars with foliar applications of salt extracted more water from soil than they did with no salt, and the drought-resistant cultivar took up more water than did the drought-sensitive cultivar. The drought-resistant cultivar with foliar NaCl maintained a higher turgor potential and extracted more water from the drying soil than did the drought-sensitive cultivar with foliar NaCl, suggesting that the drought-resistant cultivar was also more salt tolerant.     

Yield and growth responses of kenaf (Hibiscus cannabinus L.) in a semi-arid tropical environment to irrigation regimes based on leaf water potential

Summary The growth response of kenaf (Hibiscus cannabinus L.) to four irrigation schedules based on leaf water potential _l was evaluated in a semi-arid tropical environment. Total dry matter production was unaffected by regimes in which the mean value of leaf water potential _l (mean of solar noon and dawn value) did not fall below –1.26 MPa. Stem elongation was more sensitive than dry matter accumulation to plant water stress. — The economic yield for paper pulp production (i. e. total plant dry matter production minus that of the foliage and upper 60 cm of stem) increased with the frequency of irrigation. — Growth recovery by kenaf following a period of water stress was examined. Alleviation of water stress 10 weeks after irrigation, when _l was –1.60 MPa, produced stem elongation rates that were greater than those of plants previously receiving irrigation. This ability to withstand water stress and partially compensate in growth following alleviation of the stress indicates that the kenaf crop has stress response features suitable for rainfall only production under semi-arid tropical conditions. — Irrigation schedules based on _l resulted in water applications tailored to crop requirements in that water use increased, and the time interval between irrigation decreased, with increasing canopy development as well as with increasing evaporative demand. However, erratic fluctuations in _l between irrigations make scheduling by this method difficult and the use of daily mean, dawn or noon values of _l for scheduling irrigation of kenaf cannot be recommended in environments of high evaporative demand. The factors contributing to these fluctuations in (_l) are discussed.     

Photosynthesis,leaf conductance,and water relations of cowpea under saline conditions

Summary Cowpea (Vigna unguiculata L.), grown widely under both irrigated and dryland conditions, is well adapted to drought and high temperature and is moderately salt tolerant. Data on photosynthetic response and regulation of water relations in cowpea under salinity stress is lacking. Therefore, in conjunction with a field plot experiment to establish the leaching requirement of cowpea, measurements were made of carbon dioxide assimilation rates (A) by ¹⁴CO₂ uptake, leaf conductances to H₂O (g₁) by tritum uptake, and to CO₂ (g), and leaf total water potential (_t ¹) and osmotic potential ( ¹).Cowpeas, grown in field plots containing Pachappa fine sandy loam (mixed, thermic, Mollic Haploxeraff), were irrigated daily with saline water (1,350 mg 1^–1 total salt concentration) to achieve leaching fractions of 0.17, 0.13, 0.09, 0.07, and 0.02. Cowpea maintained high leaf water potentials, high rates of CO₂ assimilation and high leaf conductances under moderately saline conditions (high leaching). Values of _t ¹ and ¹ for high leaching were consistently 50 to 200 J kg^–1 higher than for low leaching throughout the day. Calculating ¹ at full leaf turgor eliminated diurnal variation in ¹. As leaching decreased, however, A, g₁, and g, decreased significantly. About 45% of the 1°C assimilated by the leaf was incorporated rapidly into ethanol insoluble compounds. The relationship between A and g₁ for cowpea was similar to that reported for other crops.Contribution from the US Salinity Laboratory, USDA-ARS, 4500 Glenwood Dr., Riverside, CA. 92501, USA     

Online-monitoring of tree water stress in a hedgerow olive orchard using the leaf patch clamp pressure probe

The need for sophisticated irrigation strategies in fruit tree orchards has led to an increasing interest in reliable and robust sensor technology that allows automatic and continuous recording of the water stress of trees under field conditions. In this work we have evaluated the potential of the leaf patch clamp pressure (LPCP) probe for monitoring water stress in a 4-year-old ‘Arbequina’ hedgerow olive orchard with 1667 trees ha⁻¹. The leaf patch output pressure (P_p) measured by the LPCP probe is inversely correlated with the leaf turgor pressure (>50 kPa). Measurements of P_p were made over the entire irrigation season of 2010 (April to November) on control trees, irrigated up to 100% of the crop water needs (ET_c), and on trees under two regulated deficit irrigation (RDI) strategies. The 60RDI trees received 59.2% of ET_c and the 30RDI trees received 29.4% of ET_c. In the case of the RDI trees the irrigation amounts were particularly low during July and August, when the trees are less sensitive to water stress. At severe water stress levels (values of stem water potential dropped below ca. −1.70 MPa; turgor pressure < 50 kPa) half-inversed or completely inversed diurnal P_p curves were observed. Reason for these phenomena is the accumulation of air in the leaves. These phenomena were reversible. Normal diurnal P_p profiles were recorded within a few days after rewatering, the number depending on the level of water stress previously reached. This indicates re-establishment of turgescence of the leaf cells. Crucial information about severe water stress was derived from the inversed diurnal P_p curves. In addition P_p values measured on representative trees of all treatments were compared with balancing pressure (P_b) values recorded with a pressure chamber on leaves taken from the same trees or neighbored trees exposed to the same irrigation strategies. Concomitant diurnal P_b measurements were performed in June and September, i.e. before and after the period of great water stress subjected to RDI trees. Results showed close relationships between P_p and P_b, suggesting that the pressure chamber measures relative turgor pressure changes as the LPCP probe. Therefore the probe seems to be an advantageous alternative to the pressure chamber for monitoring tree water status in hedgerow olive tree orchards.     

The effect of soil surface temperature on the crop water stress index

Summary A coupled soil-vegetation energy balance model which treats the canopy foliage as one layer and the soil surface as another layer was validated againt a set of field data and compared with a single-layer model of a vegetation canopy. The two-layer model was used to predict the effect of increases in soil surface temperature (T _s ) due to the drying of the soil surface, on the vegetation temperature (T _v ). In the absence of any change in stomatal resistance the impact of soil surface drying on the Crop Water Stress Index (CSWI) calculated from T _v was predicted. Field data came from a wheat crop growing on a frequently irrigated plot (W) and a plot left un watered (D) until the soil water depletion reached 100 mm. Vegetation and soil surface temperatures were measured by infrared thermometers from tillering to physiological maturity, with meteorological variables recorded simultaneously. Stomatal resistances were measured with a diffusion porometer intensively over five days when the leaf area index was between 5 and 8. The T _v predicted by the single-layer and the two-layer models accounted for 87% and 88% of the variance of measured values respectively, and both regression lines were close to the 11 relationship. Study of the effect of T _s on the CWSI with the two-layer model indicated that the CWSI was sensitive to changes in T _s . The overestimation of crop water stress calculated from the CWSI was predicted to be greater at low leaf area indices and high levels of stomatal resistance. The implications for this bias when using the CWSI for irrigation scheduling are discussed.List of Symbols C Sensible heat flux from the soil-vegetation system (W m^–2) - c _{l shade} Mean stomatal conductance of the shaded leaf area (m s^–1) - c _{l sun} Mean stomatal conductance of the sunlit leaf area (m s^–1) - c _max Maximum stomatal conductance (m s^–1) - c ₀ Minimum stomatal conductance (m s^–1) - C _p Specific heat at constant pressure (J kg^–1 °C^–1) - C _s Sensible heat flux from the soil (W m^–2) - C _v Sensible heat flux from the vegetation (W m^–2) - c _v Bulk stomatal conductance of the vegetation (m s^–1) - CWSI Crop Water Stress Index (dimensionless) - e _a Vapor pressure at the reference height (kPa) - e _b Vapor pressure at the virtual source/sink height of heat exchange (kPa) - e ₀ ^* Saturated vapor pressure at T ₀ (kPa) - e _s Vapor pressure at the soil surface (kPa) - e _v ^* Saturated vapor pressure at T _v (kPa) - G Soil heat flux (Wm^–2) - GLAI Green leaf area index (dimensionless) - GLAI_shade Green shaded leaf area index (dimensionless) - GLAI_sun Green sunlit leaf area index (dimensionless) - k Extinction coefficient for photosynthetically active radiation (dimensionless) - k ₁ Damping exponent for Eq. A 5 (m² W^–1) - LAI Leaf area index (dimensionless) - LE Latent heat flux from the soil-vegetation system (W m^–2) - LE _s Latent heat flux from the soil (W m^–2) - LE _v Latent heat flux from the vegetation (W m^–2) - p _a Density of air (kg m^–3) - PAR_a Photosynthetically active radiation above the canopy (W m^–2) - PAR_u Photosynthetically active radiation under the canopy (W m^–2) - r _a Aerodynamic resistance (s m^–1) - r _b Heat exchange resistance between the vegetation and the adjacent air boundary layer (s m^–1) - r _c Bulk stomatal resistance of the vegetation (s m^–1) - R _n Net radiation above the canopy (W m^–2) - R _s Net radiation flux at the soil surface (W m^–2) - r _st Mean stomatal resistance of leaves in the canopy (s m^–1) - R _v Net radiation absorbed by the vegetation (W m^–2) - r _w Heat exchange resistance between the soil surface and the boundary layer (s m^–1) - S Photosynthetically active radiation on the shaded leaves (W m^–2) - S _d Diffuse photosynthetically active radiation (W m ^–2) - S ₀ Photosynthetically active radiation on a surface perpendicular to the beams (W m^–2) - T _a Air temperature at the reference height (°C) - T _b Temperature at the virtual source/sink height of heat exchange (°C) - T ₀ Aerodynamic temperature (°C) - T _s Soil surface temperature (°C) - T _v Vegetation temperature (°C) - w ₀ Single scattering albedo (dimensionless) - Psychrometric constant (kPa °C) - ₀ Cosine of solar zenith angle (dimensionless)     

Nitrogen fertilizer management of cotton grown under drip irrigation in a grumusol

Summary A field experiment was carried out for two years on a grumusol (Typic chromoxerert) soil at Merhavya, Israel, to study the influence of different concentrations of N in soil solution on the growth and yield of drip-irrigated cotton (Gossypium hirsutum L.) var. Acala SJ-2. The N-concentrations in the soil solution used were: 0, 12.5, 25, 50, 75 and 100 ppm N. The soil was analyzed for moisture and NO₃-N every two weeks and the concentration of NO₃-N in the soil solution was calculated. When the NO₃-N concentration was less than the above-mentioned levels, N-fertilizer was added in the irrigation water to match these concentrations. If the tested soils showed higher concentrations, no N fertilizer was applied.The maximum yields of seed cotton obtained were 6.3 ton h^–1 in the first year, and 5.7 ton ha^–1 in the second year. Concentrations below 25 ppm N in the soil solution reduced the cotton seed and lint yields, but concentrations of 50 ppm N and above did not increase the yields and sometimes even decreased them. Application of more nitrogen caused excessive vegetative growth and less seed-cotton and lint.The results show that soil nitrate analysis during the cotton season can be used to monitor the N supplied by drip irrigation.Contribution from the Agricultural Research Organization, The Volcani Center, Bet Dagan, Israel. No. 1418-E, 1985 series     

Water relations,growth and yield of Fino lemon trees under regulated deficit irrigation

Fino lemon trees (Citrus limon L. Burm. fil.) on sour orange (Citrus aurantium L.), growing on a low water retention capacity soil, were submitted to three different irrigation treatments over four years: 100% ETc all year (T-0), 25% ETc all year except during the rapid fruit growth period when 100% ETc was applied (T-1) and 100% ETc all year, except during the rapid fruit growth period when 70% ETc was applied (T-2). A water saving of 30 and 20% was achieved in the T-1 and T-2 treatments, respectively. The plant responses to irrigation treatments were similar in all the years studied. Leaf water potential decreased during deficit irrigation periods in T-1 and T-2 treatments. Larger differences were found in values taken at predawn ( _pd) than at midday ( _md), indicating that _pd is a more useful indicator of plant water status. There was neither osmotic nor elastic adjustment in response to deficit irrigation treatment. A clear separation between the main periods of shoot and fruit growth was found, which can be considered an advantageous characteristic in applying regulated deficit irrigation strategies. Onset of the critical period of rapid fruit growth could be determined precisely by considering the decrease in relative fruit growth rate values. T-2 treatment did not induce a significant reduction in total yield, but it caused a delay in reaching marketable lemon fruit size. T-1 treatment did not affect total yield, with a reduction in yield on the first pick occurring in only one year. Chemical characteristics of lemon fruit were not significantly modified by irrigation treatment.